Engineering Materials

Engineering Materials
Introduction to Eng. Materials :

Since the earliest days of the evolution of mankind , the main
distinguishing features between human begins and other mammals has
been the ability to use and develop materials to satisfy our human
requirements. Nowadays we use many types of materials, fashioned in
many different ways, to satisfy our requirements for housing, heating,
furniture, clothes, transportation, entertainment, medical care, defense
and all the other trappings of a modern, civilised society.
Most materials doesn't exist in its pure shape , it is always exist as a
ores . During the present century the scope of metallurgical science has
expanded enormously , so that the subject can now be studied under the
following headings :
a) Physical metallurgy
b) Extraction metallurgy
c) Process metallurgy
In the recent years studying the metallurgy science gave to humanity an

ever growing range of useful alloys. Whilst many of these alloys are put
to purposes of destruction, we must not forget that others have
contributed to the material progress of mankind and to his domestic
comfort.
This understanding of the materials resources and nature enable the
engineers to select the most appropriate materials and to use them with
greatest efficiency in minimum quantities whilst causing minimum
pollution in their extraction, refinement and manufacture.
Selection of materials :
Let’s now start by looking at the basic requirements for selecting
materials that are suitable for a particular application. For example figure
1 shows a connecter joining electric cables. The plastic casing has been
partly cut away to show the metal connector. Plastic is used for the outer
casing because it is a good electrical insulator and prevents electric shock
if a person touches it. It also prevents the conductors touching each other
and causing a short circuit. As well as being a good insulator the plastic is
cheap, tough, and easily moulded to shape. It has been selected for the
casing because of these properties – that is, the properties of
1
toughness, good electrical insulation, and ease of moulding to shape. It is
also a relatively low cost material that is readily available.
The metal joining piece and its clamping screws are made from
brass. This metal has been chosen because of its special properties. These
properties are good electrical conductivity, ease of extruding to shape,
ease of machining (cutting to length, drilling and tapping the screw
threads ), adequate strength and corrosion resistance. The precious metal
silver is an even better conductor, but it would be far too expensive for
this application and it would also be too weak and soft.
Figure 1. The electrical connector.
Another example as in figure 2 shows the connecting rod of a motor

car engine. This is made from a special steel alloy. This alloy has been
chosen because it combines the properties of strength and toughness with
the ability to be readily forged to shape and finished by machining.
Figure 2. The connecting rod of motor car engine.
Thus the reasons for selecting the materials in the above examples
can be summarized as :
 Commercial factors such as:
Cost, availability, ease of manufacture.
 Engineering properties of materials such as:
Electrical conductivity, strength, toughness, ease of forming by
extrusion, forging and casting, machinability and corrosion resistance.
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Engineering Materials Msc. Shaymaa Mahmood
Engineering materials:
Almost every substance known to man has found its way into the
engineering workshop at some time or other. The most convenient way to
study the properties and uses of engineering materials is to classify them
into ‘families’ as shown in figure below:
Figure 3. classification of engineering materials.
1. Metals
1.1 Ferrous metals
 These are metals and alloys containing a high proportion of the
element iron.
 They are the strongest materials available and are used for
applications where high strength is required at relatively low cost
and where weight is not of primary importance.
 As an example of ferrous metals such as : bridge building, the
structure of large buildings, railway lines, locomotives and rolling
stock and the bodies and highly stressed engine parts of road
vehicles.
 The ferrous metals themselves can also be classified into
"families', and these are shown in figure 4.
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Engineering Materials Msc. Shaymaa Mahmood
Figure 4. Classification of ferrous metals.
1.2 Non – ferrous metals

 These materials refer to the remaining metals known to
mankind.
 The pure metals are rarely used as structural materials as they
lack mechanical strength.
 They are used where their special properties such as corrosion
resistance, electrical conductivity and thermal conductivity are
required. Copper and aluminum are used as electrical conductors
and, together with sheet zinc and sheet lead, are use as roofing
materials.
 They are mainly used with other metals to improve their
strength.
 Some widely used non-ferrous metals and alloys are classified
as shown in figure 5.
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Figure 5. Classification of non-ferrous metals and alloys.
2. Non – metallic materials

2.1 Non – metallic (synthetic materials )
These are non – metallic materials that do not exist in nature,
although they are manufactured from natural substances such as oil,
coal and clay. Some typical examples are classified as shown in figure
6.
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Figure 6. classification of synthetic materials.
 They combine good corrosion resistance with ease of manufacture

by moulding to shape and relatively low cost.
 Synthetic adhesives are also being used for the joining of metallic
components even in highly stressed applications.
2.2 Non – metallic (Natural materials )

Such materials are so diverse that only a few can be listed here to
give a basic introduction to some typical applications.
 Wood: This is naturally occurring fibrous composite material used
for the manufacture of casting patterns.
 Rubber :This is used for hydraulic and compressed air hoses and oil
seals. Naturally occurring latex is too soft for most engineering uses
but it is used widely for vehicle tyres when it is compounded with
carbon black.
 Glass : This is a hardwearing, abrasion-resistant material with

excellent weathering properties. It is used for electrical insulators,
laboratory equipment, optical components in measuring instruments
etaand, in the form of fibers, is used to reinforce plastics. It is made
by melting together the naturally occurring materials : silica (sand),
limestone (calcium carbonate ) and soda (sodium carbonate).
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 Emery : This is a widely used abrasive and is a naturally occurring
aluminum oxide. Nowadays it is produced synthetically to maintain
uniform quality and performance.
 Ceramic: These are produced by baking naturally occurring clays

at high temperatures after moulding to shape. They are used for
high – voltage insulators and high – temperature – resistant cutting
tool tips.
 Diamonds: These can be used for cutting tools for operation at high
speeds for metal finishing where surface finish is greater
importance. For example, internal combustion engine pistons and
bearings. They are also used for dressing grinding wheels.
 Oils : Used as bearing lubricants, cutting fluids and fuels.
 Silicon : This is used as an alloying element and also for the

manufacture of semiconductor devices.
These and other natural, non-metallic materials can be classified as

shown in figure 7.
Composite materials (composites )

These are materials made up from, or composed of, a combination of
different materials to take overall advantage of their different properties.
In man-made composites, the advantages of deliberately combining
materials in order to obtain improved or modified properties was
understood by ancient civilizations. An example of this was the
reinforcement of air-dried bricks by mixing the clay with straw.this
helped to reduce cracking caused by shrinkage stresses as the clay dried
out. In more recent times, horse hair was used to reinforce the plaster
used on the walls and ceiling of buildings. Again this was to reduce the
onset of drying cracks.
Nowadays, especially with the growth of the plastics industry and the
development of high-strength fibers, a vast range combinations of
materials is available for use in composites.
For example, carbon fiber reinforced frames for tennis rackets and
shafts for golf clubs have revolutionized these sports.
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Figure 7. Classification of natural materials.
Factors affecting materials properties:

The following are the more important factors which can be influence
the properties and performance of engineering materials.
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1. Heat treatment
This is the controlled heating and cooling of metals to change their
properties to improve their performance or to facilitate processing.
An example of heat treatment is the hardening of a piece of high-
carbon steel rod. If it is heated to dull red heat and plunged into cold
water to cool it rapidly (quenching), it will become hard and brittle. If it
is again heated to dull red heat but allowed to cold very slowly it will
become softer and less brittle (more tough). In this condition it is said to
be annealed.
After the heat treatment happened on the material it will be in its
best condition for flow forming, during flow forming (working) the
grains will be distorted and this will result in most metals becoming
work hardened if flow formed at room temperature. To remove any
locked in stresses resulting from the forming operations and to prepare
the material for machining, the material has to be normalized.
2. Processing
Hot –and cold working process will be referred to understand what
is meant by terms hot and cold working as applied to metals. Figure 8
shows examples of hot and cold working.
Figure 8. Examples of (a) hot-working and (b) cold-working process.
Metal is hot worked or cold worked depending upon the

temperature at which it is flow formed to shape . These temperatures are
not easy to define . for instance , lead hot works at room temperature
and can be beaten into complex shapes without cracking , but steel does
not hot work until it is red hot .
When metal are examined under the microscope it can be seen that
they consist of very small grains. When most metals are bent or worked
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at room temperature (cold worked) these grains become distorted and
the metal becomes hard and brittle .
When metals are hot worked the crystals are also distorted.
however, they reform instantly into normal crystals because the process
temperature is above the temperature of recrystallisation for the metal
being used and work hardening does not occur. this cold working is the
flow forming of metals below the temperature the recrystallisation,
whilst hot working is the flow forming of metals above the temperature
of recrystallisation.
3. Environmental reactions
The properties of materials can also be effected by reaction with
environment in which they are used. For example:
Resting of steel
Unless steel structures are regularly maintained by rest
neutralization and painting process, resting will occur. The rest will eat
into the steel, reduce its thickness and, therefore, its strength. In extreme
cases an entire structure made from steel may be eaten away.
Dezincification of brass
Brass is an alloy of copper and zinc and when brass is exposed to a
marine environment for along time, the salt in the sea water pray react
with the zinc content of the brass so as remove it and leave it behind on
spongy, porous mass of copper. This obviously weakness the material
which fails under normal working conditions.
Degradation of plastic
Many plastic degrade and become weak and brittle when exposed
to the ultraviolet content of sunlight. Special dyestuffs have to be
incorporated into the plastic to filter out these harmful rays.
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Metal Structure and Bounding in Materials :

Introduction:-
Although the properties of the metals used widely they all had one
thing in common. No matter what their composition, no matter what
changes they had gone through during extraction from the ore, refinement
and processing, they were all crystalline.
Atoms:-
Not so very long ago, in our early chemistry lessons, we used to say
that the atom was the smallest unit of which matter was composed and
was indivisible. Also the atom is considered as the basic structural unit of
matter Now, it is not quite so simple as that, and the chemist no longer
regards the atom as being in the nature of an in destructible little billiard-
ball which is held by some mysterious force of attraction to its neighbors.
Each atom is composed of a positively charged nucleus surrounded

by a sufficient number of negatively charged electrons so that the charges
are balanced and neutrons which carry no charge. The number of
electrons identifies the atomic number and the element of the atom.
When the atoms have gained or lost one or more electrons, it is called
as” Ions”. Losing of an electron makes the atom electropositive since
there will be a positively charged proton without its balancing electron.
Such an ion is called a positive ion. While gaining an electron makes the
atom electronegative since there is no spare positively charged proton in
the nucleus to balance the additional electron. Such an ion is called a
negative ion.
Chemical properties are related to the numbers of electrons and
protons present and in this respect there are altogether ninety-two
basically different types of atom which occur naturally. Of late the
scientists have succeeded in building up a series of new ones.
When two or more atoms, either of one type or of different types, are
joined together chemically, the unit which is produced is called a
molecule.
In a similar way the gases fluorine and chlorine, with seven electrons in
the outer shell in each case, have like chemical properties. Both are gases
1
(at normal temperatures and pressures) with strongly non-metallic
properties.
Many of the similarities and differences among the elements can be
explained by their respective atomic structures as shown in Figure 1.
Figure 1. Simple model of atomic structure for several elements :

(a) hydrogen , (b) helium, (c) fluorine, (d) neon, (e) sodium.
We might infer that there is a maximum number of electrons that

can be contained in a given orbit. This turns out to be correct, and the
maximum is defined by:
Maximum number of electrons in an orbit = 2 n2

where n identifies the orbit, with n = 1 closest to the nucleus.
The number of electrons in the outermost shell, relative to the

maximum number allowed, determines to a large extent the atom's
chemical affinity for other atoms. These outer shell electrons are
called valence electrons. For example, since a hydrogen atom has
only one electron in its single orbit, it readily combines with another
hydrogen atom to form a hydrogen molecule H 2. For the same
reason, hydrogen also reacts readily with various other elements (for
example, to form H2O). In the helium atom, the two electrons in its
only orbit are the maximum allowed [2n2 = 2(l)2 = 2]. and so helium
is very stable. Neon is stable for the same reason. Its outermost orbit
(n = 2) has eight electrons (the maximum allowed), so neon is an
inert gas.
In contrast to neon, fluorine has one fewer electron in its outer
shell (n =2) than the maximum allowed and is readily attracted to
other elements that might share an electron to make a more stable
set. The sodium atom seems divinely made for the situation, with
one electron in its outermost orbit. It reacts strongly with fluorine to
form the compound sodium fluoride, as pictured in Figure 2.
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Figure 2. The sodium fluoride molecule, formed by the transfer of the extra electron
of the sodium atom to complete the outer orbit of the fluorine atom.
At the low atomic numbers considered here, the prediction of the number
of electrons in the outer orbit is straightforward. As the atomic number
increases to higher levels, the allocation of electrons to the different orbits
becomes somewhat more complicated.
Bonding in Materials:
It depends on the bonding between atoms and molecules where the
atoms are held together in molecules by various types of bonds that
depends on the valence electrons. By comparison , molecules are
attracted to each other by weaker bonds, which generally result from the
electron configuration in the individual molecules.
Thus , we have the following types of bonding :
1. Ionic Bond
In the ionic bond, the atoms of one element give up their outer
electron(s), which an in turn attracted to the atoms of some other
element to increase their electron count in the outermost shell to eight,
as shown in figure 3. This bond is naturally provides a very Strong
bond between atoms and as a properties of solid materials with the
ionic bonding include low electrical conductivity and poor ductility.
Figure 3. Ionic bond .
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As an example of this bond is the Sodium chloride (table salt) is

a more common example. Because of the transfer of electrons
between the atoms, sodium and chlorine ions are formed as shown
in this reaction :
Na + + Cl ‾ → Na +Cl ‾
2. Covalent Bond
In the covalent bond, electrons are shared (as opposed to
transferred) between atoms in their outermost shells to achieve a
stable set of eight. as shown in figure 4.
Figure 4. Covalent bond.
Solids with covalent bonding generally possess high hardness and

low electrical conductivity . As an example of covalent bond the
molecule of the gas methane ( CH 4 ) , four hydrogen atoms are
combined with one carbon atom. The carbon atom has four
electrons in its outer shell, but these are joined by four more
electrons, contributed singly by each of the four hydrogen atoms as
shown in figure 5.
H
H—C—H
H
(ii)
Figure 5. (i) Covalent Bonding in a Molecule of Methane, CH4.
(ii) Chemists express the structural formula for the methane molecule.
3. Metallic Bond
It is the atomic bonding mechanism in pure metals and metal
alloys. The metallic bonding involves the sharing of outer shell
electrons by all atoms to form a general electron cloud that
permeates the entire block as shown in figure 6.
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ELECTRON 'CLOUD'
Figure 6 . Diagrammatic Representation of the "Metallic Bond".
This cloud provides the attractive forces to hold the atoms

together and form a strong, rigid structure in most cases. Because
of the general sharing of electrons and their freedom to move
within the metal, metallic bonding provides typical properties of
materials characterized such as good electrical conductivity , good
conduction of heat and good ductility.
4. Van der Waal’s Force

They are very small forces of attraction acting between atoms in
cases where the formation of ionic or covalent bonds is not
possible.
Basically similar forces also act between atoms which are already
bounded in neighboring molecules , giving rise to weak Van der
Waal’s forces between long-chain molecules in polymers.
Crystalline Structures :
Many substances, including metals, have a crystalline structure in the
solid state. Metal crystals from when the molten metals cools and
solidifies, where as crystals of other substances, for example copper
sulphate, and sodium chloride ( salt ), form when a saturated solution of
compound evaporates causing the solid to crystallize out.
In crystalline structure , the atoms are located at regular and recurring
positions in three dimension . The pattern may be replicated millions of
times within a given crystal. The structure can be viewed in the form of a
unit cell, which is the basic geometric grouping of atoms that is repeated.
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There are several types of pattern in which metallic atoms can
arrange them selves on solidification , but the most common is as follows
:-
1. Body-Centered-Cubic [BCC]
As shown in figure 7 (a), as an example of the materials for this
type :
Chromium, Molybdenum, Niobium, Tungsten, Iron.
2. Face-Centered-Cubic [FCC]
As shown in figure 7 (b), as an example of the materials for this
type :
Aluminum, Copper, Lead, Nickel, Iron, Gold, Silver.
3. Hexagonal-Closed-Packed [HCP]
As shown in figure 7 (c), as an example of the materials for this
type :
Beryllium, Cadmium, Magnesium, Zinc.
(a) (b) (c)

Figure 7 The three principle types of structural in which metallic elements crystallize :
(a) Body-Centered-Cubic (b) Face-Centered-Cubic (c) Hexagonal-Closed-Packed.
There are some metals that are undergo a change of structure at

different temperatures. Iron metal for example is arranged in a body-
centered-cubic ( BCC ) at room temperature, when the metal is heated
and reaches a temperature of 910˚C, the atoms rearrange themselves into
Face-Centered-Cubic ( FCC ) crystals. If the metal is heated to the still
higher temperature of 1400˚C the atoms again rearrange themselves, this
time back into Body-Centered-Cubic form.
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Noncrystalline (Amorphous) Structures:
The noncrystalline solids materials do not have their basic particles
arranged in a geometric patter. Their particles have a random formation,
and such as a result, such substances are said to be amorphous (without
shape).
Many important materials are noncrystalline: liquids and gases, for
example. Water and air have a noncrystal structures. A metal loses its
crystalline structure when it is melt. Such as glass, plastics and rubber are
materials that fall into this category. While many important plastics are
mixture of crystalline and noncrystalline forms.
Two closely related features differentiate noncrystalline from

crystalline materials :-
1. Absence of long – range order in the molecular structure of a
noncrystalline. It can be visualized with reference to figure 8. They
closely packed and repeating pattern of the crystal structure and
random arrangement of atoms in the noncrystalline materials.
Figure 8. Difference in structure between (a) crystalline and (b) noncrystalline

materials.
2. Differences in melting and thermal expansion characteristics. It

could be demonstrated by a metal when it is melts. When the metal
is molten an increase in volume compared to the material’s solid
crystalline state. This effect is characteristic most materials when
melted ( a noble exception is ice; liquid water is denser than ice).
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The crystalline state :

As we mention before, that all of the metals and its alloys have
crystalline structure where the atoms are rearranged in an organized
shapes which it is called as the crystal lattice. This lattice consisted of
another smallest grouping of atoms each one is called the unit cell as
shown in figure 9.
Figure 9. Representation of part of a space lattice with a unit cell outlined.
The unit cell is the smallest parallel surfaces of the crystalline

structure that can be removed or repeated in different directions. It is also
differ from each other in shape or size in the crystalline lattice from one
material to another.
The atoms that belongs to the unit cell are called the basic atoms, its
number is different from one shape of arrangement to another, this
number can be found from the following equation:-
N = NC + NI + NF
where N : is the number of the basic atoms in the unit cell.
NC : is the number of the atoms in the corner.
NI : is the number of the atoms in side the cube.
NF : is the number of the atoms in the center of the face.
For the Body-centered-cubic (BCC), it is obvious that the unit cell

have just two atoms the first one in the corner of the cube and the second
in the center of the cube (that share the unit cell with each atom in the
corner ) as in the equation:
N = 8* 1/8 + 1 = 2
As for the Face-centered-cubic (FCC) it is calculated by the equation
below:
N = 8 * 1/8 + 6 * 1/2 = 4
Finally for the Hexagonal-closed-packed (HCP) is also calculated as
follows :
N = 12 * 1/6 + 3 + 2 * 1/2 = 6
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The atomic packing factor [A.P.F]:

It can be defined as the ratio between the volume of the basic atoms
of the unit cell (which represent the volume of all atoms in one unit cell )
to the volume of the unit cell it self.
For cubic crystals, there is one constant to be quoted. The unit cell
constant of pure metal crystals can be directly related to the atomic
diameter of the element as below:-
1. Body-centered-cubic (BCC)
In the body centered cubic the length of the cube diagonal = 2 D ,
as shown in figure 10, and by Pythagoras :
(2D)2 = a2 + 2a2
 D= 3a & r= D
2 2
3
 r  a
4
The volume of the atom can be calculated as follows :
V  4r3  4( 3a)3
3 3 4
The volume of the basic atoms in the unit cell can be calculated as
follows :
Vb 2[ 4 3a)3 ]
(
3 4
The volume of the unit cell is Vu = a3

2[ 4  ( 3 a)3]
A .P .F .  V b  3 4 = 0.68
Vu a3
where D : is the atomic diameter
a : is the lattice constant
r : is the atomic radius
Figure 10. Body centered cubic unit cell. Relation between a and D.
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2. Face-centered-cubic (FCC)
Similarly, for face centered cubic as shown in figure 11, the
length of a face diagonal = 2D and by Pythagoras:
(2D)2 = a2 + a2
 D= 1 a & r= D
2 2
1
 r  a
2 2
The volume of the basic atoms in the unit cell can be calculated as
follows :
Vb  4[ 4 ( 1 a)3 ]
3 2 2
The volume of the unit cell is : Vu = a3
4 [4  ( 1 a)3]
3 2 2
A.P.F. = 0.74
a3
Figure 11. Face centered cubic unit cell. Relation between a and D.
3. Hexagonal-closed-packed (HCP)
There are two lattice constant, a and c as shown in figure 12, that
parameter a is equal to one atomic diameter [a = D] , the parameter
c is the high of the hexagonal structure. From the hexagonal
structure basics :
a
c = 1.633 , r =
a 2
so the volume of the basic atoms is :
4 a
V b 6 [ ( )3]a3
3 2
and the volume of the unit cell is :
3 3 2 3 3
Vu  a .c  1 . 633 a3
2 2
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A .P .F .  a3  0 .74
3 3  1 .633 a 3
Figure 12. Hexagonal structure with unit cell outlined, and showing
relationship between a and c.
Example :
The atomic radius of an iron atom is 1.238 * 10-10 m. Iron crystallizes as
BCC. Calculate the lattice parameter of the unit cell, a. How many atoms
are contained within the BCC unit cell ? Also find the atomic packing
factor ?
For BCC unit cell
4
a  r
3
For iron r = 1 . 238  10  10 m
Therefore
4  1 . 238  10  10
a   2 . 861  10  10 m
3
There are 9 atoms 8 in the corners and 1 in the center of the

cubic. And the
V 2[ 4  ( 3 a ) 3 ]
A .P .F .  b  3 4 = 0.68
V 3
u a
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General Properties of Engineering Materials

The principle properties of materials which are of importance to the
engineer in selecting materials. These can be broadly divided into:
Physical properties of materials

These properties concerned with such properties as melting,
temperature, electrical conductivity, thermal conductivity, density,
corrosion resistance, magnetic properties, etc. and the more important
of these properties will be considered as follows :
1. Density
Density is defined as mass per unit volume for a material. The
derived unit usually used by engineers is the kg/m3 . Relative density
is the density of the material compared with the density of the water
at 4˚C. The formulae of density and relative density are:
density ( )  mass (m)
volume (V )
Density of the material
Relative density (d) =
Density of pure water at 4˚C
2. Electrical conductivity
Figure 1 shows a piece of electrical cable. In this example copper
wire has been chosen for the conductor or core of the cable because
copper has the property of very good electrical conductivity. That is,
it offers very little resistance to the flow of electrons (electric
current) through the wire. A plastic materials such as polymerized
has been chosen for the insulating sheathing surrounding the wire
conductor. This material has been chosen because it is such a bad
conductor, where very few electrons can bass through it. Because
they are very bad conductors they are called as insulators. There is
no such thing as a perfect insulator, only very bad conductors.
Figure 1. Electrical conductivity.
For example, metallic conductors of electricity all increase in

resistance as their temperatures rise. Pure metal shows this effect
more strongly than alloys. However, pure metals generally have a
better conductivity than alloys at room temperature. The
conductivity of metals and metal alloys improves as the temperature
falls.
Conversely, non-metallic materials used for insulators tend to
offer a lower resistance to the passage of electrons, and so become
poorer insulators, as their temperatures rise. Glass, for example, is an
excellent insulator at room temperature, but becomes a conductor if
raised to red heat.
3. Melting temperature of material

The melting temperatures and the recrystallisation temperatures
have a grate effect on the materials and the alloys of the materials
properties and as a result on its applications.
4. Semiconductors
So far we have examined the conductivity of the metals and the
insulating properties of the non-metals (exception : carbon). In
between conductors and isolators lies a range of materials known as
semiconductors. These can be good or bad conductors depending
upon their temperatures. The conductivity of semiconductor
materials increases rapidly for relatively small temperature increases.
This enable them to be used as temperature sensors in electronic
thermometers.
Semiconductor materials are capable of having their conductors
properties changed during manufacture. Examples of semiconductor
materials are silicon and germanium. They are used extensively in
the electronics industry in the manufacture of solid-state devices
such as diodes, thermistors, transistors and integrated circuits.
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5. Thermal conductivity
This is the ability of the material to transmit heat energy by
conduction. Figure 2 shows a soldering iron. The bit is made from
copper which is a good conductor of heat and so will allow the heat
energy stored in it to travel easily down to the tip and into the work
being soldered. The wooden handle remains cool as it has a low
thermal conductivity and resists the flow of heat energy.
Figure 2. Thermal conductivity.
6. Fusibility
This is the ease with which materials will melt. It can be seen
from figure 3 that solder melts easily and so has the property of high
fusibility. On the other hand, fire bricks used for furnace linings only
melt at very high temperatures and so have the properties of low
fusibility. Such materials which only melt a very high temperatures
are called refractory materials. These must not be confused with
materials which have a low thermal conductivity and used as thermal
insulators. Although expanded polystyrene is an excellent thermal
insulator, it has a very low melting point ( high fusibility ) and in no
way can it be considered a refractory material.
Figure 3. Fusibility.
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7. Reluctance (as magnetic properties)
Just as some materials are good or bad conductors of electricity,
some materials can be good or bad conductors of magnetism. The
resistance of magnetic circuit is referred to as reluctance. The good
magnetic conductors have low reluctance and examples are the
ferromagnetic materials which get their name from the fact that they
are made from iron, steel and associated alloying elements such as
cobalt and nickel. All other materials are non-magnetic and offer a
high reluctance to the magnetic flux felid.
8. Temperature stability
Any changes in temperature can have very significant effects on
the structure and properties of materials. However, there are several
effects can appear with changes in temperature such as creep.
Creep is defined as the gradual extension of a material over a
long period of time whilst the applied load is kept constant. It is also
an important factor when considering plastic materials, and it must
be considered when metals work continuously at high temperatures.
For example gas-turbine blades. The creep rate increases if the
temperature is raised, but becomes less if the temperature is lowered.
Mechanical properties of materials

These properties are concerned with the following properties :
1. Tensile strength TS
It is the ability of a material to withstand tensile ( stretching )
loads without breaking. For example, figure 4 shows a heavy load
being held up by a rod fastened to beam. As the force of gravity
acting on the load is trying to stretch the rod, the rod is said to be
in tension. Therefore, the material from which the rod is made
needs to have sufficient tensile strength to resist the pull of the
load.
Strength: is the ability of a material to resist applied forces
without fracturing.
Figure 4. Tensile Strength
٤
2. Toughness
It is the ability of the materials to withstand bending or it is
the application of shear stresses without fracture, so the rubbers
and most plastic materials do not shatter, therefore they are tough.
For example, if a rod is made of high-carbon steel then it will be
bend without breaking under the impact of the hammer, while if a
rod is made of glass then it will broken by impact loading as
shown in figure 5.
Figure 5. Toughness (Impact Resistance).

.
3. Malleability
It is the capacity of substance to withstand deformation under
compression without rupture or the malleable material allows a
useful amount of plastic deformation to occur under compressive
loading before fracture occurs. Such a material is required for
manipulation by such processes as forging, rolling and rivet
heading as shown in figure 6.
Figure 6. Malleability
4. Hardness
It is the ability of a material to withstand scratching
(abrasion) or indentation by another hard body , it is an indication
of the wear resistance of the material. For example, figure 7 shows
a hardened steel ball being pressed first into a hard material and
then into a soft material by the same load. As seen that the ball
only makes a small indentation in the hard material but it makes a
very much deeper impression in the softer material.
٥
Figure 7. Hardness.
5. Ductility
It refer to the capacity of substance to undergo deformation
under tension without rupture as in wire drawing (as shown in
figure 8 ), tube drawing operation.
Figure 8. Ductility
6. Stiffness
It is the measure of a material's ability not to deflect under an
applied load. For example, although steel is very much stronger
than cast iron, then the cast iron is preferred for machine beds and
frames because it is more rigid and less likely to deflect with
consequent loss of alignment and accuracy.
Consider figure 9 (a): for a given load the cast iron beam deflect
less than the steel beam because cast iron is more rigid material.
However, when the load increased as shown in figure 9 (b), the
cast iron beam will break, whilst the steel beam deflects little
further but not break. Thus a material which is rigid is not
necessarily strong.
٦
Figure 9. Stiffness (rigidity):

(a) The tested materials deflect under a light load
(b) The tested materials deflect under a heavy load.
7. Brittleness
It is the property of a material that shows little or no plastic
deformation before fracture when a force is applied. Also it is
usually said as the opposite of ductility and malleability.
8. Elasticity
It is the ability of a material to deform under load and return to
its original size and shape when the load is removed. If it is made
from an elastic material it will be the same length before and after
the load is applied, despite the fact that it will be longer whilst the
load is being applied. All materials posses elasticity to some
degree and each has its own elastic limits. As in figure 10.
Figure 10. Elasticity.
٧
9. Plasticity
This property is the exact opposite to elasticity, while the
ductility and malleability are particular cases of the property of the
plasticity . It is the state of a material which has been loaded
beyond its elastic limit so as to cause the material to deform
permanently. Under such conditions the material takes a permanent
set and will not return to its original size and shape when the load
is removed. When a piece of mild steel is bent at right angles into
the shape of a bracket, it shows the property of plasticity since it
dose not spring back strength again, this is shown in figure 11.
Figure 11. Plasticity.

Some metals such as lead have a good plastic range at room
temperature and can be extensively worked (where working of
metal means squeezing, stretching or beating it to shape). This is
advantage for plumber when beating lead flashings to shape on
building sites.
٨
Materials Testing
Introduction:
Testing of materials are necessary for many reasons, and the subject
of materials testing is very broad one. Some of the purpose for the testing
of materials are:
1. To determine the quality of a material. This may be one aspect of
process control in production plant.
2. To determine such properties as strength, hardness, and ductility.
3. To check for flaws within a material or in a finished component.
4. To assess the likely performance of the material in a particular
service condition.
It is obvious that there is not one type of test that will provide all the
necessary information about a material and its performance capabilities,
and there are very many different types of test that have been devices for
use in the assessment of materials. One of the most widely tests is the
tensile test to destruction. In this type of test a test-piece of standard
dimensions is prepared, and this is then stressed in un axial tension. Other
tests that are often used for the determination of strength data are
compression, torsion, hardness, creep and fatigue tests. With the
exception of harness tests, these are all test of a destructive nature and
they normally require the preparation of test-pieces to certain standard
dimensions.
For the detection of flaws or defects within part-processed stock
material, or within finished components, there are several non-destructive
test techniques available. In addition, there are many special tests that
have been devised for the purpose of assessing some particular quality of
material, or for obtaining information on the possible behavior of
component or assembly in service.
In spite of the properties of materials where introduced, then the
composition, processing and heat treatment of a range of metallic and
non-metallic materials widely used by the engineer have been described,
we should more be able to understand the problems and techniques
associated with the testing of materials properties because they can be,
nonetheless, useful to the designer, fabricator, and research worker, as
follow:
1. Tensile test
The main principle of the tensile test is denotes the resistance of a
material to a tensile load applied axially to a specimen.
There are a several tensile testing machine, as in figure 1 (a) shows a
popular bench-mounted tensile testing machine, whilst figure 1(b) shows
a more sophisticated machine suitable for industrial and research
laboratories, while in figure 1(c) shows the schematic drawing of a tensile
– testing apparatus. These machines are capable of performing
compression, shear and bending tests as well as tensile tests.
(a) (b) (c)

Figure 1. Tensile testing machines.
It is very important to the tensile test to be considered is the standard

dimensions and profiles are adhered to.
The typical progress of tensile test can be seen in figure 2 .
Figure 2. Typical progress of a tensile test: (1) beginning of test, no load; (2)
uniform elongation and reduction of cross-sectional area; (3) continued elongation,
maximum load reached; (4) necking begins, load begins to decrease; and (5)
fracture. If pieces are put back together as in (6), final length can be measured.
٢
Let's now look at Figure 3. In this figure, the gauge length (L0) is the
length over which the elongation of the specimen is measured. The
minimum parallel length (Lc) is the minimum length over which the
specimen must maintain a constant cross-sectional area before the test
load is applied. The lengths L0. Lc, Li. and the cross-sectional area (A) are
all specified in BS 18.
Figure 3. Properties of tensile test specimens: (a) cylindrical; (b) flat.
The elongation obtained for a given force depends upon the length and
area of the cross-section of the specimen or component, since:
elongation = appliedforce  L
EA
where L = length
A = cross-sectional area
E = elastic modulus
Therefore if the ratio [ L/A ] is kept constant (as it is in a proportional test
piece), and E remains constant for a given material, then comparisons can
be made between elongation and applied force for specimens of different
sizes.
٣
Tensile test results:
Let's now look at the sort of results we would get from a typical tensile
test on a piece of annealed low-carbon steel. The load applied to the
specimen and the corresponding extension can be plotted in the form of a
graph, as shown in Figure 4 .
Figure 4. Load-extension curve for a low-carbon steel.
 From A to B the extension is proportional to the applied load. Also, if

the load is removed the specimen returns to its original length. Under
these relatively lightly loaded conditions the material is showing elastic
properties.
 From B to C it can be seen from the graph that the metal suddenly extends
with no increase in load. If the load is removed at this point the metal will
not spring back to its original length and it is said to have taken
a permanent set. Therefore, B is called "limit of proportionality ", and if
the force is increased beyond this point a stage is reached where a sudden
extension takes place with no increase in force. This is known as the
" yield point" C.
 The yield stress is the stress at the yield point; that is, the load at B divided
by the original cross-section area of the specimen. Usually, a designer
works at 50 per cent of this figure to allow for a 'factor of safety'.
 From C to D extension is no longer proportional to the load, and if the
load is removed little or no spring back will occur. Under these
relatively greater loads the material is showing plastic properties.
 The point D is referred to as the 'ultimate tensile strength' when referred
extension graphs or the 'ultimate tensile stress' (UTS) when
٤
referred to stress-strain graphs. The ultimate tensile stress is calculated
by dividing the load at D by the original cross-sectional area of the
specimen. Although a useful figure for comparing the relative strengths
of materials, it has little practical value since engineering equipment is
not usually operated so near to the breaking point.
 From D to E the specimen appears to be stretching under reduced load
conditions. In fact the specimen is thinning out (necking) so that the
'load per unit area' or stress is actually increasing. The specimen finally
work hardens to such an extent that it breaks at E.
 In practice, values of load and extension are of limited use since they
apply to one particular size of specimen and it is more usual to plot the
stress-strain curve.
 Stress and strain are calculated as follows:
stress( )  load
areaofcross  section
extension
steain( ) 
originallength
The tensile test experimental results on some materials:

The interpretation of tensile test data requires skill borne out of
experience, since many factors can affect the test results - for instance, the
temperature at which the test is carried out, since the tensile modulus and
tensile strength decrease as the temperature rises for most metals and
plastics, whereas the ductility increases as the temperature rises. The test
results are also influenced by the rate at which the specimen is strained.
Figure 5 shows a typical stress-strain curve for an annealed mild steel.
From such a curve we can deduce the following information.
 The material is ductile since there is a long elastic range.
 The material is fairly rigid since the slope of the initial elastic range
is steep.
 The limit of proportionality (elastic limit) occurs at about 230 MPa.
 The upper yield point occurs at about 260 MPa.
 The lower yield point occurs at about 230 MPa.
 The ultimate tensile stress (UTS) occurs at about 400MPa.
٥
Figure 5. Typical stress-strain curve for annealed mild steel.
Figure 6 shows a typical stress-strain curve for a grey cast iron. From
such a curve we can deduce the following information.
 The material is brittle since there is little plastic deformation before it
fractures.
 A gain the material is fairly rigid since the slope of the initial elastic range
is steep.
 It is difficult to determine the point at which the limit of proportionality
occurs, but it is approximately 200 MPa.
 The ultimate tensile stress (UTS) is the same as the breaking stress for this
sample. This indicates negligible reduction in cross-section (necking) and
minimal ductility and malleability. It occurs at approximately 250 MPa.
Figure 6. Typical stress-strain curve of grey cast iron.
The yield point, however, is possibly of greater importance to the

engineer than the tensile strength itself, so it becomes necessary to specify a
stress which corresponds to a definite amount of permanent extension as a
substitute for the yield point. This is commonly called the "Proof Stress",
and is derived as shown in figure 7. A line BC is drawn parallel to the line of
proportionality, from a predetermined point B. the stress corresponding to C
٦
will be the proof stress in the case illustrated it will be known as the "0.1 %
Proof stress", since AB has been made equal to 0.1 % of the gauge length.
The material will fulfil the specification therefore if, after the proof force is
applied for fifteen seconds and removed, a permanent set of not more than
0.1 % of the gauge length has been produced. Proof lengths are commonly
0.1 %and 0.2 % of the gauge length, depending upon the type of alloy.
The time limit of 15 seconds is specified in order to allow sufficient time
for extension to be complete under the proffer force.
Figure 7. Method used to obtain the 0.1 % proof stress.
Figure 8 shows a typical stress-strain curve for a wrought light alloy.

From this curve we can deduce the following information:
 The material has a high level of ductility since it shows a long plastic
range.
 The material is much less rigid than either low-carbon steel or cast iron
since the slope of the initial plastic range is much less steep when plotted
to the same scale.
 The limit of proportionality is almost impossible to determine, so the
proof stress will be specified instead. For this sample a 0.2 per cent proof
stress is approximately 500 MPa (the line AB).
٧
Figure 8. Typical stress-strain curve of a light alloy.
It is important to determine the properties of polymeric materials

which are may ranged from highly plastic to the highly elastic. As in
figure 9 the stress-strain curves for polymeric materials have been
classified in to five main groups by Carswell and Nason.
Figure 9. Typical stress-strain curves for polymers.
A tensile test can also yield other important facts about a material
under test. For example, it can enable the elastic modulus (E) for the
material to be calculated.
The physicist Robert Hooke found that within its elastic range the
strain produced in a material is proportional to the stress applied. It was
left to Thomas Young to quantify this law in terms of a mathematical
constant for any given material.
strain α stress
٨
therefore stress = constant (E)
strain
This constant term (E) is variously known as 'Young's modulus', the
'modulus of elasticity' or the 'tensile modulus'. Thus:
tensile or compressive stress

E = ‫ـــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
strain
(force)/(original cross-sectional area)

= ‫ـــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
(change in length)/(original length)
Example 1 :
Calculate the modulus of elasticity for a material which produces the
following data when undergoing test:
Applied load = 35.7 kN, Cross-sectional area = 25mm2, Gauge length =
28 mm, Extension = 0.2 mm.
E = stress
strain
Where
35.7kN
stress (σ) = = 1.428 MPa
and 0.2mm
strain (ε) = = 0.007
35.7  28 2
therefore E= = 199.92 kN / mm
25  0.2
= 200 GPa (approx.)

This would be a typical value for a low-carbon steel.
It was stated earlier that malleability and ductility are special cases of the
types of plasticity.
 Malleability This refers to the extent to which a material can undergo
deformation in compression before failure occurs.
 Ductility This refers to the extent to which a material can undergo
٩
deformation in tension before failure occurs.
All ductile materials are malleable, but not all malleable materials are
ductile since they may lack the strength to withstand tensile loading.
Therefore ductility is usually expressed, for practical purposes, as the
percentage; Elongation in gauge length of a standard test piece at the
point of fracture when subjected to a tensile test to destruction.
increase in length
Elongation % = ------------------------------ x 100
original length
The increase in length is determined by fitting the pieces of the fractured
specimen together carefully and measuring the length at failure.
increase in length (elongation) = length at failure — original length
Figure 10 shows a specimen for a soft, ductile material before and

after testing. It can be seen that the specimen does not reduce in cross-
sectional area uniformly, but that server local necking occurs prior to
fracture. Since most of the plastic deformation and, therefore, most of the
elongation occurs in the necked region, doubling the gauge length dose
not double the elongation when calculated as a percentage of gauge
length. Therefore it is important to use a standard gauge length if
comparability between results is to be achieved.
Elongation is calculated as follows :
Figure 10. Elongation.
Lu  Lo
Elongation % = 100
Lo
١٠
Example 2:
Calculate the percentage elongation of a 70/30 brass alloy, if the original
gauge length (L0) is 56 mm and the length at fracture ( Lu) is 95.2 mm.
L  Lo
Elongation % = u 100
Lo
95.2  56
= 100 = 70 %
56
2. The compression test

Because of the presence of submicroscopic cracks, brittle materials are
often weak in tension, as tensile stress tends to propagate those cracks which
are oriented perpendicular to the axis of tension. The tensile strengths they
exhibit are low and usually vary from sample to sample. These same
materials can nevertheless be quite strong in compression. Brittle materials
are chiefly used in compression, where their strengths are much higher. A
schematic diagram of a typical compression test is shown in figure 11.
Figure 11. Compression test of ductile material.
Figure 12. shows a comparison of the compressive and tensile strengths

of gray cast iron and concrete, both of which are brittle materials.
Figure 12. Tensile and compressive engineering stress-strain curves for gray cast iron
and concrete.
١١
Because the compression test increase the cross-sectional area of the
sample, necking never occurs. Extremely ductile materials are seldom
tested in compression because the sample is constrained by friction at the
points of contact with the plants of the apparatus. This constraint gives
rise to a complicated stress distribution which can only be analyzed in an
approximate fashion.
3. Ductility testing
The percentage elongation, as determined by the tensile test, has
already been discussed as a measure of ductility. Another way of
assessing ductility is a simple bend test. There are several ways in which
this test can be applied, as shown in figure 13. The test chosen will
depend upon the ductility of the material and the severity of the test
required.
 Close bend test The specimen is bent over on itself and flattened. No
allowance is made for spring back, and the material is satisfactory if the
test can be completed without the metal tearing or fracturing. This also
applies to the following tests.
 Angle bend test The material is bent over a former and the nose radius
of the former and the angle of bend (θ˚) are fixed by specification.
Again no allowance is made for spring back.
 180 ˚ bend test This is a development of the angle bend test using a flat
former as shown. Only the nose radius of the former is specified.
Figure 13. Bend tests: (a) close bend; (b) angle bend; (c) 180 :C bend.
١٢
4. Impact testing (toughness testing)

Impact tests consist of striking a suitable specimen with a controlled
blow and measuring the energy absorbed in bending or breaking the
specimen. The energy value indicates the toughness of the material under
test.
Figure 14 shows a typical impact testing machine which has a hammer
that is suspended like a pendulum, a vice for holding the specimen in the
correct position relative to the hammer and a dial for indicating the
energy absorbed in carrying out the test in joules (J).
When the heavy pendulum, released from a known height, strikes and
breaks the sample before it continues its upward swing. From knowledge
of the mass of the pendulum and the difference between the initial and
final heights, the energy absorbed in fracture can be calculated, as shown
in figure 15 the schematic drawing of the impact test machine.
Figure 14. Typical impact testing machine.
Figure 15. Schematic drawing of standard impact-testing apparatus.
١٣
Figure 16 shows how a piece of high carbon steel rod will bend when
in the annealed condition, after hardening and lightly tempering, the same
piece of steel will fracture when hit with a different hammer.
Figure 16. Impact loading: (a) a rod of high-carbon (1.0%) steel in the annealed
(soft) condition will bend struck with a hammer (UTS 925 MPa); (b) after
hardening and lightly tempering, the same piece steel will fracture when
hit with a hammer despite its UTS having increased to 1285 MPa.
There are several types of the impact tests and the most famous type is
the Izod test.
In the Izod test, a 10mm square, notched specimen is used, it is
preferred to use a specimen that have a more than one or two and even
three notched in the same specimen. The striker of the pendulum hits the
specimen with a kinetic energy of 162.72 J at a velocity of 3.8m/s. Figure
17 shows details of the specimen and the manner in which it is supported.
Figure 17. Izod test (a/I dimensions in millimeters); (a) detail of notch; (b) section
of test piece (at notch); (c) position of strike.
Since test use a notched specimen, useful information can be

obtained regarding the resistance of the material to the spread of a crack
which may originate from a point of stress concentration such as sharp
comers, undercuts, sudden changes in section, and machining
١٤
marks in stressed components. Such points of stress concentration
should be eliminated during design and manufacture.
A second type of impact test is the Charpy test. While in the Izod test
the specimen is supported as a cantilever, but in the Charpy test it is
supported as a beam. It is struck with a kinetic energy of 298.3 J at a
velocity of 5m/s. The Charpy impact test is usually use for testing the
toughness of polymers. Figure 18 shows details of the Charpy tes:
manner in which it is supported.
Figure 18. Charpy test (all dimensions in millimeters).
The effects of temperature on the materials mechanical

properties:
The temperature of the specimen at the time of making the test also
has an important influence on the test results. Figure 19 hows the
embrittlement of low-carbon steels at refrigerated temperatures, and
hence their unsuitability for use in refrigeration plant and space vehicles.
Figure 19. Effect of test temperatures on toughness.
١٥
The impact test is also useful as a production tool in comparing
manufactured materials with others which have proved satisfactory in
service. Steels, like most other BCC metals and alloys, absorb more
energy when they fracture in a ductile fashion rather than in a brittle
fashion. On this account the impact test is often used to assess the
temperature of the transition from the ductile to brittle state which occurs
as the temperature is lowered. The transition temperature is also
dependent on the shape of the notch in the specimen. For identical
materials, the sharper the notch, the higher the apparent transition
temperature. The results of impact tests for several materials are shown
in figure 20.
Figure 20. Impact test results for several alloys over a range of testing temperatures.
5. Creep test
Even at constant stress, materials continue to deform for an indefinite
period of time. This time – dependent deformation is called creep. At
temperatures less than 40 percent of the absolute melting point, the extent
of creep is negligible, but at temperatures higher than this it becomes
increasingly important. It is for this reason that the creep test is
commonly thought of as a high-temperature test.
The majority of creep testing is conducted in the tensile mode, and the
type of test-piece used is similar to the normal tensile test-piece. Most
creep testing is carried out under constant-load conditions and utilizes
dead weights acting through a simple lever system. In the creep testing an
extensometer readings are noted at regular time interval s until the
required a mount of data has been obtained, or until the test-piece
fractures, depending on whether the object of the test is to determine the
creep rate or to determine the total creep strain.
One of the difficulties in creep testing is that a single test may take a
very long time to complete (10000 hours is 417 days), and there are
١٦
serious difficulties in attempting to extrapolate from the results of
comparatively short-term tests to assess the probable behavior of a
material over a 10 or 20 year period of service.
Modern creep-testing laboratories may contain several hundred
creep-testing machines in continuous use.
Also creep is sensitive to both the applied load and the testing
temperature, as shown in figure 21: increasing stress raises the level of
the creep curve, and increasing temperature, which accelerates recovery
processes, increase the creep rate.
Figure 21. The effects of stress and temperature on creep behavior.
6. Hardness testing
Hardness has already been defined as the resistance of a material to

indentation or abrasion by another hard body ( good hardness generally
means that the material is resistant to scratching and wear) . It is by
indentation that most hardness tests are performed. A hard indenter is
pressed into the specimen by a standard load, and the magnitude of the
indentation (either area or depth) is taken as a measure of hardness.
Hardness tests are commonly used for assessing material properties
because they are quick and convenient. However, a variety of testing
methods is appropriate due to differences in hardness among different
materials. The most well known hardness tests are Brinell and Rockwell.
١٧
1. The Brinell hardness test
In this test, hardness is measured by pressing a hard steel ball into the
surface of the test piece, using a known load. It is important to choose the
combination of load and ball size carefully so that the indentation is free
from distortion and suitable for measurement. The relationship of the
Brinell hardness [HB] which is between load P (kg), the diameter D (mm)
of the hardened ball indenter and the diameter d (mm) of the indentation
on the surface is given by the expression:
Load (Kg)
HB = ‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
Area of curved surface of indentation
P(Kg)
HB =
1 2 2 2
2  D[D  D  d ](mm )
P
For different materials, the ratio D2 has been standardized in order to
obtain accurate and comparative results such as :
P
K=
D2
Where K is. a constant; typical values of K are:
Ferrous metals K = 30
Copper and copper alloys K = 10
Aluminum and aluminum alloys K=5
Lead, tin and white-bearing metals K=1
Figure 22 shows how the Brinell hardness value is determined. The
diameter of the indentation is measured in two directions at right angles
and the average taken. The diameter is measured either by using a
microscope scale, or by a projection screen with micrometer adjustment.
Figure 22. Principle of the Brinell hardness test.
١٨
To ensure consistent results, the following precautions should be
observed.
 The thickness of the specimen should be at least seven times the depth of
the indentation to allow unrestricted plastic flow below the indenter.
 The edge of the indentation should be at least three times the diameter of
the indentation from the edge of the test piece.
 The test is unsuitable for materials whose hardness exceeds 500 HB, as
the ball indenter tends to flatten.
There are a definite relationship between strength and hardness so it is
possible to measure the tensile strength from the hardness test.
2. The Vickers hardness test

This test is preferable to the Brinell test where hard materials are
concerned, as it uses a diamond indenter. (Diamond is the hardest material
known - approximately 6000 HB.) The diamond indenter is in the form of a
square-based pyramid with an angle of 1 36˚ between opposite faces.
Since only one type of indenter is used the load has to be varied for
different hardness ranges. Standard loads are 5, 10, 20. 30, 50 and 1 00
kg. It is necessary to state the load when specifying a Vickers hardness
number. For example, if the hardness number is found to be 200 when
using a 50 kg load, then the hardness number is written as HV (50) = 200.
Figure 23 shows the measuring screen for determining the distance
across the corners of the indentation. The screen can be rotated so that
two readings at right angles can be taken and the average is used to
determine the hardness number (HD). This is calculated by dividing the
load by the projected area of the indentation:
Load (Kg)
Hv = ‫ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــ‬
Surface area of indentation (mm2)
P(Kg)
Hv = 1
2
[d 2sin (136)](mm 2 )
= 2P sin 68 = 1.854 P

d2d2
where P is the load in Kg and d (mm) is the diagonal of the
impression made by the indenter made by the diamond.
١٩
Figure 23. The Vickers hardness test method: (a) universal hardness-testing machine;
(b) measuring screen showing magnified of Vickers impression.
3. The Rockwell hardness test

Although not as reliable as the Brinell and Vickers hardness tests for
laboratory purposes, the Rockwell test is widely used in industry as it is
quick, simple and direct reading. Universal electronic hardness testing
machines are now widely used which, at the turn of a switch, can provide
either Brinell, Vickers or Rockwell tests and show the hardness number as
a digital readout automatically. They also give a "hard copy' printout of
the test result together together with the test conditions and date.
In principle the Rockwell hardness test compares the difference in

depth of penetration of the indenter when using forces of two different
values. That is, a minor force is first applied (to take up the backlash and
pierce the skin of the component) and the scale are set to read zero. Then
a major force is applied over and above the minor force and the increased
depth of penetration is shown on the scales of the machine as a direct
reading of hardness without the need for calculation or conversion tables.
Figure 24 shows a typical Rockwell hardness testing machine.
The standard Rockwell test can not be used for very thin sheet and
foils and for these the Rockwell superficial hardness test is used.
٢٠
Figure 24. The Rockwell hardness test.
4. Shoe Scleroscope
The test piece must be small enough to mount in the testing machine,
and hardness is measured as a function of indentation. However, the
scleroscope is not like other types of hardness tests based their measure
on the ratio of applied load divided by the resulting impression are [ like
Brinell and Vicker well] or by the depth of impression [ like Rock well].
The scleroscope is an instrument that measures the rebound height of a
hammer droped from a certain distance above the surface of the material
to be tested. The hammer consist of a weight with diamond indenter
attached to it. The scleroscope therefore measures the mechanical energy
absorbed by the material when the indenters strikes the surface. The
energy absorbed gives an indication of resistance to penetration, which
matches our definition of hardness. As shown in figure 25.
The primary use of the sclerscope seems to be in measuring the

hardness of large parts of steel, large rolls, casting and gears. And since
the seclroscope can be carried to the work piece, it is useful for testing
large surfaces and other components which could not easily be placed on
the testing tables of any other testing machines.
Figure 25. Shore scleroscope.
٢١
The table below shows the different in the ways of measuring the
hardness numbers for methods we mentioned above.
Table 1. Hardness tests.
٢٢
Surface Hardening of Steel

Introduction:
The service conditions of many steel components such as cams and
gears, make it necessary for them to possess both hard, wear-resistant
surfaces and, at the same time, tough, shock-resistant cores.
In plain carbon steels these two different sets of properties exist only in
alloys of different carbon content. A low-carbon steel, containing
approximately 0-1% carbon, will be tough, whilst a high-carbon steel of
0-9% or more carbon will possess adequate hardness when suitably heat-
treated.
The situation can best be met by employing a low-carbon steel with
suitable core properties and then causing either carbon or nitrogen to
penetrate to a regulated depth into the surface skin; as in the principal
surface-hardening processes of carburising and nitriding.
Alternatively, a steel of medium carbon content and in the normalised
condition can be used, local hardness at the surface then being introduced
by one or other of the name-hardening processes.
In the first case the hardenable material is localised, whilst in the
second case it is the heat-treatment itself which is localised.
There are four main types of the surface hardening which are :-
1. Case hardening
2. Nitriding
3. Flam hardening
4. Induction hardening
The first two types include a change in the chemical structure of the
surface while the other types include a change in the micro constituents as
a result for the positional heat treatment.
1. Case hardening
Is one of the most used for producing a hard surface on a ductile
steel. It involves the introduction of additional carbon into the surface of
mild steel, effectively producing a composite material consisting of low
carbon steel with a thin case, about 0.5 – 0.7 mm in thickness, of high
carbon steel, this was the principle of case-hardening that have been used
for centuries in the conversion of mild or wrought iron to steel by the
cementation process.
The case-hardening consists in surrounding the component with
suitable carbon material and heating it to above its upper critical
temperature for long enough to produce a carbon enriched layer of
sufficient depth.
Solid, liquid and gaseous carburizing media are used. The nature and
scope of the work involved will govern which media is best to employ.
The case-hardening process has two distinct steps, as shown in figure 1:
 Carburising ( the additional of carbon)
 Heat treatment ( hardening and core refinement)
Figure 1. Case hardening : (a) carburising, (b) after carburising, (c) after
quenching component.
1. Carburising
Carburizing makes use of the fact that low carbon steel absorb
carbon when heated to the austenitic condition various carbonaceous
materials are used in the carburizing process as follows:-
1.1 Carburising in solid media

"Pack-carburising", as it is usually called, involves packing the
components into cast-iron or steel boxes along with the carburizing
material so that a space of approximately 50 mm exists between the
components. The lids are then luted on to the boxes, which are slowly
٢
heated to the carburizing temperature for between 900 and 950ْ C.
they are maintained at this temperature for up to five hours, according
to depth of case required.
Carburising media vary in composition, but consist essentially of
some carbonaceous material, such as wood or bone charcoal or
charred leathers together with an energiser which may account for up
to 40% of the total composition. This energiser is usually a mixture of
sodium carbonate ("soda ash") and barium carbonate, and its purpose
is to accelerate the solution of carbon by the surface layer of the steel.
It is thought that carburisation proceeds by dissociation of carbon
monoxide which will be present in the hot box. When the gas comes
into contact with the hot steel it dissociates thus:
2CO CO2 + C
The atomic carbon deposited at the surface of the steel dissolves
easily in the metal. In this method of carburizing the thickness of the
surface is between 0.05 – 1.55 mm.
If it is necessary to prevent any areas of the component from being
carburised, this can be achieved by electro-plating these areas with
copper to a thickness of 0-075-0-10 mm; carbon being insoluble in
solid copper at the carburising temperature.
When carburising is complete the components are quenched or
cooled slowly in the box, according to the nature of the subsequent
heat-treatment to be applied.
1.2 Carburising in a liquid bath ( Cyaniding)
Liquid-carburising is carried out in baths containing from 20 to

50% sodium cyanide, together with up to 40% sodium carbonate and
varying amounts of sodium chloride.
This cyanide-rich mixture is heated in pots to a temperature of 870-
950° C, and the work, which is contained in wire baskets, is immersed
for periods varying from about five minutes up to one hour, depending
upon the depth of case required.
One of the main advantages of cyanide-hardening is that
pyrometric control is so much more satisfactory with a liquid bath.
Moreover, afte r treatment the basket of work can be quenched. This
not only produces the necessary hardness but also gives a clean
surface to the components.
٣
The process is particularly useful in obtaining shallow cases of 0.1
– 0.25 mm.
Dissociation of the carbon monoxide at the steel surface then takes
place with the same result as in pack-carburising. The nitrogen, in
atomic form, also dissolves in the surface and produces an increase in
hardness by the formation of nitrides as it does in the nitriding
process.
Cyanides are, of course, extremely poisonous, and every
precaution should be taken to avoid inhaling the fumes from a pot.
Every pot should be fitted with an efficient fume-extracting hood.
Likewise the salts s hould in no circumstances be allowed to come
into contact with an open wound. Needless to say, the consumption of
food by operators whilst working in the shop containing the cyanide
pots should be Absolutely forbidden.
1.3 Carburising by gaseous media
Gas-carburising is carried out in both batch-type and continuous

furnaces. The components are heated at about 900° C for three or four
hours in an atmosphere containing gases which will deposit carbon
atoms at the surface of the components. The most important of these
gases are the hydrocarbons methane CH4 , and propane, C3H8.
They should be of high purity in order to avoid the deposit of oily
soot which impedes carburising. To facilitate better gas circulation and
hence, greater uniformity of treatment the hydrocarbon is mixed
with a "carrier" gas. This is generally an "endothermic" type of
atmosphere made in a generator and consisting of a mixture
containing mainly nitrogen, hydrogen and carbon monoxide.
The relative proportions of hydrocarbon and carrier are adjusted to
give the desired carburizing rate. Thus, the concentration gradient of
carbon in the surface can be "flattened" by prolonged treatment in a
less rich carburising atmosphere. Control of this type is possible only
with gaseous media.
Gas-carburising is becoming increasingly popular, particularly for
the mass production of thin cases. Not only is it a neater and cleaner
process but the necessary plant is more compact for a given output.
Moreover, the carbon of the surface layers can be controlled more
accurately and easily with thickness of about 0.25 – 1.0 mm.
2. Heat treatment after Carburising
٤
If carburising has been correctly carried out, the core will still be of
low carbon content (0.1 – 0.2% carbon), whilst the case should have a
maximum carbon content of 0.83% carbon (the eutectoid composition),
Figure 2. Heat-treatment After Carburising.

A Indicates the temperature of treatment for the core, and B the temperature of
treatment for the case.
Considerable gain growth occurs in the material during a carburizing

treatment, therefore a three stage of heat treatment must be given to the
carburized parts to produce the desired final properties. This heat
treatment involves:
2.1 Refining the core
The component is first heat-treated with the object of refining the
grain of the core, and consequently toughening it. This is effected by
heating it to just above its upper critical temperature (about 870° C for
the core) when the coarse ferrite-pearlite structure will be replaced by
refined austenite crystals. The component is then water-quenched, so
that a fine ferrite-martensite structure is obtained.
The core-refining temperature of 870° C is, however, still high above
the upper critical temperature for the case, so that, at the quenching
temperature, the case may consist of large austenite grains. On
٥
quenching these will result in the formation of coarse brittle martensite.
Further treatment of the case is therefore necessary.
2.2 Refining the case

The component is now heated to about 760° C, so that the coarse
martensite of the case changes to fine-grained austenite. Quenching then
gives a fine-grained martensite in the case.
At the same time the martensite produced in the core by the initial
quench will be tempered somewhat, and much will be reconverted into
fine-grained austenite embedded in the ferrite matrix (point C in
Figure.2). The second quench will produce a structure in the core
consisting of martensite particles embedded in a matrix of ferrite grains
surrounded by bainite. The amount of martensite in the core is reduced
if the component is heated quickly through the range 650-760° C and
then quenched without soaking. This produces a core structure
consisting largely of ferrite and bainite, and having increased toughness
and shock-resistance.
2.3 Tempering
The component is tempered at about 200 – 220 ° C to relieve any
quenching strains present in the case.
2. Nitriding
The process is used to put a hard, wear-resistant (‫ )ﻰﻠﺒﻟا ﺔﻣوﺎﻘﻣ‬coating on
components made from special alloy steels, for example, drill bushes.
The alloy steels used for this process contain either 1.0% aluminium, or
traces of molybdenum, chromium and vanadium. Nitrogen gas is
absorbed into the surface of the metal to form very hard nitrides. The
process consists of heating the components in ammonia gas at between
500 and 600 °C for upwards of 40 hours.
At this temperature the ammonia gas breaks down and the atomic
nitrogen is readily absorbed into the surface of the steel. The case is
applied to the finished component. No subsequent grinding is possible
since the case is only a few micrometres thick. However, this is no
disadvantage since the process does not affect the surface finish of the
component and the propcess temperature is too low to cause distortion.
Some of the advantages of nitriding are:
Carking and distortion are eliminated since the processing
٦
temperature is relatively low and there is no subsequent quenching.
 Surface hardnesses as high as 1150 HD are obtainable with

'Nitralloy' steels.
 Corrosion resistance of the steel is improved.
 The treated components retain their hardness up to 500 °C
compared with the 220 °Cfor case-hardened plain carbon and low-
alloy steels.
 Resistance to fatigue is good.
 The process is cheap when large number of components are to be
treated.
As disadvantage of nitriding is more expensive than that with case-

hardening, so that the process is economical only when large number of
components are to be treated.
Carbonitriding. This is a surface-hardening process which makes use of
a mixture of carburising gases and ammonia. It is sometimes known as
"dry cyaniding" — a reference to the fact that a mixed carbide-nitride
case is produced as in the ordinary liquid cyanide pro-cess. The relative
proportions of carbon and nitrogen in the case can be varied by
controlling the ratio of ammonia to hydrocarbons in the treatment
atmosphere.
3. Flame hardening
Localised surface hardening can also be achieved in medium- and
high-carbon steels and some cast irons by rapid local heating and
quenching. Figure 3 shows the principle of flame hardening. A carriage
moves over the work piece so that the surface is rapidly heated by an oxy-
acetylene or an oxy-propane flame. The same carriage carries the water-
quenching spray. Thus the surface of the work piece is heated and
quenched before its core can rise to the hardening temperature. This
process is often used for hardening the slideways of machine tools, such
as gears, spindles and pins, that are confidently treated by this process,
since they can be spun between centers.
٧
Figure 3. Surface hardening with flame hardening (Shorter process).
4. Induction hardening
These processes are similar in principle to flame-hardening, except
that the component is held stationary- whilst the whole of its surface is
heated simultaneously by electro-magnetic induction, as shown in figure
4. The component is surrounded by an inductor block through which a
high-frequency current in the region of 2ooo Hz, passes. This raises the
temperature of the surface layer to above its upper critical in a few
seconds. The surface is then quenched by pressure jets of water which
pass through holes in the inductor block.
Thus, as in flame-hardening, the induction processes make use of the
existing carbon content (which must be above 0-4%), whilst in both case-
hardening and nitriding an alteration in the composition of the surges
layer of the steel takes place.
Figure 4. Surface hardening with induction hardening.
٨
Phase Equilibrium Diagrams
Phase equilibrium diagram is a graphic relationship between

temperature and weight ratios of elements and alloys contribute to the built of
the diagram.
Where Phase is a uniform part of an alloy, having a certain chemical
composition and structure, and which is separated from other alloy
constituents by a phase boundary.
For example the salt – water solution have a four possible phases:
- Water vapor (steam)
- Liquid salt solution (sodium chloride in water)
- Crystals of water (ice)
- Crystals of salt (sodium chloride)
Alloying systems :
Alloy is a metal composing of a mixture of elements. Most of alloys are
composed of a base metal with small amounts of additives or alloying
elements. The typical examples of alloys are steel/cast iron (iron base alloys),
bronze/brass (copper base alloys), aluminum alloys, nickel base alloys,
magnesium base alloys, titanium alloys.
There are many types of alloying systems which they are:
- Binary system
It means that alloying have two metals only.
- Ternary system
It means that alloying have three metals only.
- Multi system
It means that alloying have three and more than that metals.
The constituent components of most commercially available binary alloys

are completely soluble in each other in the liquid (molten) state and, in
general, do not form intermetallic compounds. (The exceptions being some
bearing metals.) However, upon cooling into the solid state, binary alloys can
be classified into the following types.
 Simple eutectic type The two components are soluble in each other in the
liquid state but are completely insoluble in each other in the solid state.
 Solid solution type The two components are completely soluble in each
other both in the liquid state and in the solid state.
 Combination type The two components are completely soluble in the
liquid state, but are only partially soluble in each other in the solid state.
Thus this type of alloy combines some of the characteristics of both the
previous types, hence the name ‘combination type’ phase equilibrium
diagram.
Let's now consider these three types of binary alloy systems and their
phase equilibrium diagrams in greater detail.
1) Phase equilibrium diagrams (Eutectic type):
In general case, consider for studying a two components presents which
are referred to as metal A and metal B, with the phase diagram as shown
in figure 1.
2
Figure 1. Phase equilibrium diagram (eutectic type).
Although they are mutually soluble in the liquid state, both components
retain their individual identities of crystals of A and crystals of B in the
solid state, If you refer to figure 1, you can see that the line joining the
points where solidification begins is referred to as the liquidus and that the
line joining the points where solidification is complete is referred to as the
solidus.
This type of equilibrium diagram gets its name from the fact that at one
particular composition (E), the temperature at which solidification
commences is a minimum for the alloying elements present. With this
composition the liquidus and the solidus coincide at the same temperature,
thus the liquid changes into a solid with both A crystals and B crystals
forming instantaneously at the same temperature. This point on the
diagram is called the eutectic, the temperature at which it occurs is the
eutectic temperature, and the composition is the eutectic composition.
In practice, few metal alloys from simple eutectic type phase diagrams. It
is identical with this type of phase diagram is produced for a salt (sodium
chloride) and water solution, it is total solubility of the salt in water in the
liquid state and total insolubility (crystals of ice and separate crystals of salt)
in the solid state. As an example of eutectic are carbon steels .
3
2) Phase equilibrium diagrams (Solid solution type):

Solid solution is a phase, where two or more elements are completely
soluble in each other.
Depending on the ratio of the solvent (matrix) metal atom size and solute
element atom size, two types of solid solutions may be formed:
substitution or interstitial.
Substitution solid solution
If the atoms of the solvent metal and solute element are of similar sizes
(not more, than 15% difference), they form substitution solid solution,
where part of the solvent atoms arc substituted by atoms of the alloying
element as shown in figure 2.
Figure 2. Substitution solid solution.
Interstitial solid solution
If the atoms of the alloying elements are considerably smaller, than the
atoms of the matrix metal, interstitial solid solution forms, where the
matrix solute atoms are located in the spaces between large solvent atoms
4
Figure 3. Interstitial solid solution.
When the solubility of a solute element in interstitial solution is

Exceeded, a phase of intermediate compound forms. These compounds
(WC, Fe3C etc.) play important role in strengthening steels and other
alloys.
Some substitution solid solutions may form ordered phase where ratio
between concentration of matrix atoms and concentration of alloying
atoms is close to simple numbers like AuCu 3 and AuCu.
Solid solution formation usually causes increase of electrical resistance
and mechanical strength and decrease of plasticity of the alloy.
In this type as shown in figure below the line marked liquids joins the
points where solidification commences, whilst the line marked solidus
joins the points where solidification is complete. This time there is no
eutectic composition. It has already been stated that copper and nickel are
not only mutually soluble in the liquid (molten) state, they are a/so
mutually soluble in the solid state and they form a substitutional solid
solution. The phase equilibrium diagram for copper-nickel alloys is shown
in figure 4.
5
Figure 4. Copper-nickel phase equilibrium diagram.
3) Phase equilibrium diagrams (Combination type):

Many metals and non-metals are neither completely soluble in each
other in the solid state nor are they completely insoluble. Therefore they
form a phase equilibrium diagram of the type shown in figure 5. In this
system there are two solid solutions labelled α and β. The use of the Greek
letters α, β, γ, etc., in phase equilibrium diagrams may be defined, in
general, as follows:
 A solid solution of one component A in an excess of another
component B, such that A is the solute and B is the solvent, is
referred to as solid solution α.
 A solid solution of the component B in an excess of the component
A, so that B now becomes the solute and A becomes the solvent, is
referred to as solid solution β.
 In a more complex alloy, any further solid solutions or intermetallic
compounds which may be formed would be referred to by the
subsequent letters of the Greek alphabet. That is, γ, β, etc.
6
Figure 5. Combination type phase equilibrium diagram.
We will steady the iron-carbon phase diagram as an example on the phase

equilibrium diagram which it describes the iron-carbon system of alloys,
containing up to 6.67 % carbon, discloses the phases compositions and their
transformations occurring with the alloys during their cooling or heating, as
shown in figure 6.
Carbon content 6.67 % corresponds to the fixed composition of the iron
carbide Fe3C .
7
Figure 6. Iron-carbon phase diagram.
8
The following phases are involved in the transformation, occurring with
iron-carbon alloys:
L Liquid solution of carbon in iron.

δ ferrite solid solution of carbon in iron. Maximum concentration of carbon
in δ-ferrite is 0.09 % (1493˚C) temperature of the peritectic transformation.
The crystal structure of δ-ferrite is BCC (cubic body centered).
Austenite interstitial solid solution of carbon in γ-iron. It has FCC (cubic face
centered) crystal structure, permitting high solubility of carbon up to 2.06
% at (1147˚C). It dose not exist below (723˚C) and maximum carbon
concentration at this temperature is 0.83 % .
α – ferrite solid solution of carbon in α-iron . It has BCC crystal structure

and low solubility of carbon up to 0.25 % at (723˚C). It is exists at room
temperature.
Cementite iron carbide, intermetallic compound, having fixed composition
Fe3C. It is a hard and brittle substance, influencing on the properties of steel
and cast irons.
The following phase transformations occur with iron-carbon alloys:
Alloys, containing up to 0.51% of carbon, start solidification with

formation of crystals of δ-ferrite. Carbon content in δ-ferrite increases up to
0.09% in course solidification, and at (1493°C) remaining liquid phase and δ-
ferrite perform peritectic transformation, resulting in formation of austenite.
Alloys, containing carbon more than 0.51%, but less than 2.06%, form
primary austenite crystals in the beginning of solidification and when the
temperature reaches the curve ACM primary cernentite stars to form.
Iron-carbon alloys, containing up to 2.06% of carbon, arc called Steels.

Alloys, containing from 2.06 to 6.67% of carbon, experience eutectic
transformation at (1147 °C). The eutectic concentration of carbon is 4.3% .
9
In practice only hypoeutectic alloys are used. These alloys (carbon content
from 2.06% to 4.3%) are called cast irons. When temperature of an alloy
from this range reaches 2097 °F (1147 °C), it contains primary austenite
crystals and some amount of the liquid phase. The latter decomposes by
eutectic mechanism to a fine mixture of austenite and cementite, called
ledeburite.
All iron-carbon alloys (steels and cast irons) experience eutectoid

transformation at (723°C), The eutectoid concentration of carbon is
0.83%.
When the temperature of an alloy reaches (723°C), austenite transforms to

pearlite (fine ferrite-cementite structure, forming as a result of decomposition
of austenite at slow cooling conditions).
Critical temperatures
 Upper critical temperature (point) A3 is the temperature, below

which ferrite starts to form as a result of ejection from austenite in the
hypoeutectoid alloys.
 Upper critical temperature (point) ACM is the temperature, below

which cementite starts to form as a result of ejection from austenite in
the hypereutectoid alloys.
 Lower critical temperature (point) A1 is the temperature of the

austenite-to-pearlite eutectoid transformation. Below this temperature
austenite does not exist.
 Magnetic transformation temperature A2 is the temperature

below which a-ferrite is ferromagnetic .
10
Phase compositions of the iron-carbon alloys at room
temperature:
 Hypoeutectoid steels (carbon content from 0 to 0.83%) consist of
primary (proeutectoid) ferrite (according to the curve A3) and pearlite.
 Eutectoid steel (carbon content 0.83%) entirely consists of

pearlite.
 Hyperelltectoid steels (carbon content from 0,83 to 2.06%)

consist of primary (proeutectoid)cementite (according to the curve
ACM) and pearlite.
 Cast irons (carbon content from 2.06% to 4.3%) consist of

proeutectoid cementite CT ejected from austenite according to the
curve ACM , peaiiite and transformed ledeburite (ledeburite in
which austenite transformed 10 pearlite).
11
Heat treatment of carbon steel
Introduction :
Plain carbon steels and alloy steels are among the relatively few
engineering materials which can be usefully heat treated in order to vary their
mechanical properties. The other main group is the heat-treatable aluminium
alloys. Steels can be heat treated because of the structural changes that can
take place within solid iron-carbon alloys. The various heat-treatment
processes appropriate to plain carbon steels are:
 Annealing.
 Normalising.
 Hardening.
 Tempering.
In all the above processes the steel is heated slowly to the appropriate
temperature for its carbon content and then cooled. It is the rate of cooling
which determines the ultimate structure and properties that the steel will
have, providing that the initial heating has been slow enough for the steel to
have reached phase equilibrium at its process temperature. Figure 1 shows
the types of the ranges of carbon steels.
1
Figure 1. Heat-treatment temperature Ranges of Classes of Carbon Steels in Relation to the

Equilibrium Diagram.
1. Annealing
All annealing processes are concerned with rendering steel soft and
ductile so that it can be cold worked and/or machined. There are three basic
annealing processes, as shown in figure 2, and these are:
 Stress-relief annealing at subcritical temperatures.
 Spheroidised annealing at subcritical temperatures.
 Full annealing for forgings and castings.
The process chosen depends upon the carbon content of the steel, its
pretreatment processing, and its subsequent processing and use.
2
Figure 2. Annealing temperature for plain carbon steel .
a) Stress-relief annealing
It is also called 'process annealing' , 'interstage annealing' and sub-
critical annealing, it is often used for softening cold worked low carbon
(0.4 % carbon content) steel or mild steel . To fully anneal such a steel
would involve heating to a temperature of more than 900˚C, with
consequent high cost. In a mild steel ferrite makes up about 90 % of the
structure, and the recrystallisation temperature of cold worked ferrite is
only about 500˚C. annealing a cold worked mild steel in the
temperature range 550 – 600 ˚C will result in complete recrystallisation
of ferrite, although the cold worked pearlite will be largely unaffected.
Frequently, however, we must apply a considerable amount of cold-
work to mild steels, as, for example, in the drawing of wire. Stress-relief
annealing then becomes necessary to often the metal so that further
drawing operations can be carried out. Such annealing is carried out at
about 650° C. Since this temperature is well above the recrystallisation
temperature of 500° C, recrystallisation \vill be accelerated so that it will
be complete in a matter of minutes on attaining the maximum
temperature.
3
It should be noted that process annealing is a sub-critical operation,
that is, it takes place below the lower critical temperature (Ai). For this
reason, although recrystallisation is promoted, there is no phase change
and the constituents ferrite and cementite remain present in the structure
throughout the process.
Process annealing is generally carried out in either batch-type or
continuous furnaces, usually with an inert atmosphere of burnt coal gas,
though cast-iron annealing "pots" are still used, their lids being luted on
with clay.
b) Spheroidised annealing
The Spheroidised condition is produced by annealing the steel at a
temperature between 650 and 700 ْ C, just below the lower critical
temperature. During this treatment cementite forms as spheroidal partisles
in a ferrite matrix, putting the steel into a soft, but very tough, condition.
Since the temperature involved are sub critical no phase changes take
place and spheroidisation of the cementite is purely a surface tension
effects. This is referred to as the a spheroidisation of pearlitic cementite
and the process is shown diagrammatically in figure 3.
Figure 3. The Spheroidisation of Pearlitic Cementite.
4
c) Full annealing
It is the treatment given to produce the softest possible condition in a
hypoeutectoid steel. It involves heating the steel to a temperature within
the range 30 – 50 ْ C above the upper critical temperatures and then
allowing the steel to cool slowly within the furnace. This produces a
structure containing coarse pearlite.
This results in the formation of fine grains of austenite that transform
into relatively fine grains of ferrite and pearlite or pearlite and cementite
(depending upon the carbon content) as the steel is slowly cooled to
room temperature, usually in the furnace.
Full annealing is an expensive treatment and when it is not absolutely
essential for the steel to be in a very soft condition, but a reasonably soft
and ductile material is required, the process known as normalizing is
used instead.
Ferrite, which then begins to precipitate in accordance with the
equilibrium diagram, deposits first at the grain boundaries of the
austenite, thus revealing, in the final structure, the size of the original
austenite grains. The remainder of the ferrite is then precipitated along
certain crystallographic planes within the lattice of the austenite. This
gives rise to a directional precipitation of the ferrite, as shown in figure
4. and Plate , representing typically what is known as a Widmanstatten
structure. This type of structure was first encountered by Widmanstatten
in meteorites, which may be expected to exhibit a coarse structure in
view of the extent to which they are overheated during their passage
through the upper atmosphere. .The mesh-like arrangement of ferrite in
the Widmanstatten structure tends to isolate the stronger pearlite into
separate patches, so. that strength, and more particularly toughness, are
impaired. The main characteristics of such a structure are, therefore,
weakness and brittle-ness, and steps must be taken to remove it either by
heat-treatment or by mechanical working. Hot-working will effectively
break up this coarse as-cast structure and replace it by a fine-grained
material, but in this instance we are concerned with retaining the actual
shape of the casting. Heat-treatment must therefore be used to effect the
necessary refinement of grain.
5
Figure 4. The structural effects of heating a steel casting to a temperature just above its
upper critical , followed by cooling to room temperature.
This operation need a very specific controlling on the heat

temperature of annealing because if any fault is occrous, it will make
some un desired phases in the steel such as :-
1) Over heating
Overheating during annealing, or heating for too long a period in the
austenitic range, will obviously cause grain growth of the newly formed
austenite crystals, leading to a structure almost as bad as the original
Widmanstatten structure. For this reason the requisite annealing
temperature should not be exceeded, and the
6
casting should remain in the austenitic range only for as long as is
necessary to make it completely austenitic. In fact, castings are
sometimes air-cooled to about 650° C and then cooled more slowly to
room temperature, by returning to a furnace to prevent stresses due to
rapid cooling from being set up.
2) Burning (Excessive over heating)

Excessive overheating will probably cause oxidation, or
"burning", of the surface, and the penetration by oxide films of the
crystal boundaries following ecarburization of the surface.
Such damage cannot be repaired by heat-treatment, and the castings

can only be scrapped. To prevent "burning", castings are often annealed
in cast-iron boxes into which they are packed with lime, sand, cast-iron
turnings or carbonaceous material, according to the carbon content of
the castings.
3) Under-qunealing
As the lower critical temperature (723 ْ C) is reached on heating,
the patches of pearlite change to austenite, but these crystals of
austenite are very small, since each grain of pearlite gives rise to a
number of new austenite crystals. As the temperature rises, the
Widmanstatten-type plates of ferrite are dissolved by the austenite
until, when the upper critical temperature is reached, the structure
consists entirely of fine-grained austenite. Cooling causes re-
precipitation of the ferrite, but, since the new austenite crystals are
small, the precipitated ferrite will also be distributed as small particles.
Finally, as the lower critical temperature is reached, the remaining
small patches of austenite will transform to pearlite.
7
2. Normalising
The process resembles full annealing except that, whilst in annealing
the cooling rate is deliberately retarded, in normalising the cooling rate is
accelerated by taking the work from the furnace and allowing it to cool in
free air. Provision must be made for the free circulation of cool air, but
draughts must be avoided.
In the normalising process, as applied to hyper-eutectoid steels, it can be
seen that the steel is heated to approximately 50ْ C above the upper critical
temperature line. This ensures that the transformation to fine grain austenite
corrects any grain growth or grain distortion that may have occurred
previously. Again, the steel is cooled in free air and the austenite transforms
into fine grain pearlite and cementite. The fine grain structure resulting
from the more rapid cooling associated with normalising gives improved
strength and toughness to the steel but reduces its ductility and malleability.
The increased hardness and reduced ductility allows a better surface finish
to be achieved when machining. (The excessive softness and ductility of
full annealing leads to local tearing of the machined surface.)
The type of structure obtained by normalising will depend largely upon

the thickness of cross-section, as this will affect the rate of cooling. Thin
sections will give a much finer grain than thick sections, the latter often
differing little in structure from an annealed section.
Although highly successful, this procedure tied up an excessive amount
of working capital and space and nowadays heat treatment is preferred as
the work in progress is turned round more quickly.
8
3. Hardening
When a piece of steel, containing sufficient carbon, is cooled rapidly
from above its upper critical temperature it becomes considerably harder
than it would be if allowed to cool slowly.
This involves rapidly quenching the steel, from a high temperature into
oil or water. Hypereutectoid steels are heated to (30- 50 ْ C) above the upper
critical temperature prior to quenching. It is possible that some cementite
grain boundaries.
Consequently, hypereutectoid steels are hardened by quenching from
(30- 50 ْ C) above the lower critical temperature. At this temperature the
structure because one of spheroidal cementite partictes in an austenite
matrix.
The degree of hardness produced can vary, and is dependent upon such
factors as the initial quenching temperature; the size of the work; the
constitution, properties and temperature of the quenching medium; and the
degree of agitation and final temperature of the quenching medium.
To harden apiece of steel, it must be heated then quenched in some

media which will produce in it the desired rate of cooling . the medium
used will depend upon the composition of the steel and the ultimate
properties required.
The quenching medium is chosen according to the rate at which it is
desired to cool the steel. The following list of media is arranged in order of
quenching speeds:
5 % Caustic soda
5 – 20 % Brine
Cold water
Warm water
Mineral oil.
9
4. Tempering
A quench-hardened plain carbon steel is hard, brittle and hardening
stresses are present. In such a condition it is of little practical use and it has to
be reheated, or tempered, to relieve the stresses and reduce the brittleness.
This temperature will remove internal stress setup during quenching,
remove some, or all, of the hardness, and increase the toughness of the
material.
Tempering causes the transformation of martensite into less brittle
structures. Unfortunately, any increase in toughness is accompanied by
some decrease in hardness. Tempering always tends to transform the
unstable martensite back into the stable pearlite of the equilibrium
transformations.
Tempering temperatures below 200 °C only relieve the hardening
stresses, but above 220 ْ C the hard, brittle martensite starts to transform
into a fine pearlitic structure called secondary troostite (or just
'troostite'). Troostite is much tougher although somewhat less hard than
martensite and is the structure to be found in most carbon-steel cutting tools.
Tempering above 400 ْ C causes any cementite particles present to "ball-
up" giving a structure called sorbite. This is tougher and more ductile than
troostite and is the structure used in components subjected to shock loads
and where a lower order of hardness can be tolerated, for example springs.
It is normal to quench the steel once the tempering
For most steels, cooling form the tempering temperature may be either
cooling in air, or quenching in oil or water. Some alloy steels, however,
may be become embrittled if slowly cooled temperature has been reached.
from the tempering temperature, and these steels have to be quenched.
10
Cast Iron
Introduction :
Cast iron is the name given to those ferrous metals containing more than
1.7 % carbon. It is similar in composition to crude pig iron as produced by
the blast furnace. Unlike steel, it is not subjected to an extensive refinement
process. After the pig iron has been remelted in a cupola furnace ready for
casting, selected scrap iron and scrap steel added to the melt to give the
required composition.
Although normal grades of cast iron are not particularly strong, and are
quite brittle, they are widely used as engineering materials, because of their
cheapness, ease of melting and casting, very good machineable and a high
damping capacity, resistance to wear and compressive strength are required,
it has a high fluidity which makes it easy to cast into intricate shapes and it
has a melting point between 1147 and 1250ْ C, which is substantially lower
than the melting point for mild steel.
The complete iron carbon diagram as in figure 1, it will be noticed that a
eutectic of austenite and cementite which contains 4.3% carbon is formed at
1131° C. (This eutectic point, like the eutectoid composition in the case of
steel at 0.83% carbon, may be moved farther to the left of the diagram by the
elements present, so that a cast iron containing less than 4-3% carbon may be
of eutectic composition.) In accordance with the equilibrium diagram, a cast
iron containing more than the eutectic amount of carbon may be expected to
begin solidification by depositing some cementite. Unless cooling is very
rapid, however, graphite may precipitate instead, due to instability of the
cementite caused by other elements (notably silicon) present. This primary
graphite, which separates out from the melt during cooling, forms as large
flakes, usually called "kish". The finer flakes of graphite occurring in grey
cast iron are those which are formed by decomposition of the cementite after
solidification Graphite flakes of this
latter type exist in cast irons of compositions either above or below the
eutectic, and produce rather better mechanical properties.
The presence of graphite gives a softer iron which machines well because
of the effect of the graphite flakes in forming chip cracks in advance of the
edge of the cutting tool.
Figure 1.The phase equilibrium diagram of the iron.
As for figure 2. shows that there is a eutectic when there is 4.3% carbon
present. At this composition the molten metal solidifies at 1147ْ C into
austenite (γ phase) and cementite (Fe3C). Unless cooling is very rapid,
graphite will be precipitated out due to the instability of the cementite as a
result of some of the impurities present (particularly silicon ). As cooling
proceeds, further graphite is precipitated out from the austenite. At 723ْ C
providing cooling is slow enough, the remaining austenite (γ phase) changes
into ferrite (α phase). Thus at room temperature the composition consists of
ferrite plus large flakes of graphite together with fine flakes of graphite
formed by the decomposition of the cementite after solidification.
2
Figure 2. Section of the iron-carbon phase equilibrium diagram.
For the relationship between carbon content, microstructure and mechanical

properties figure 3 is shown below.
3
4
Figure 3. Diagram showing the relationship between carbon content, microstructure and
mechanical properties of plain carbon steels in the normalized condition.
The structure of cast iron is affected by the following factors:-

a) The rate of solidification. Slow rates of solidification allow for graphite
formation and castings made in sand moulds tend to solidify gray. More
rapid solidification will tend to give white irons structures. Metal chills
are sometimes inserted into parts of sand moulds in those areas where a
high surface hardness is required.
b) Carbon content. The higher the carbon content of the iron, the greater
will be the tendency for it to solidify grey.
c) The presence of other elements. Some elements promote the formation
of graphite in an iron structure. Silicon and nickel have strong
graphitising tendencies, as shown in figure 4.
Figure 4. Effect of silicon and carbon content on the structure of cast irons.
d) The effect of heat treatment. The prolonged heating of a white iron will
cause graphitization to occur. This phenomenon is used as the basis for
the production of malleable irons. Graphite is less dense than cementite
and, if cementite decomposes into ferrite and graphite during service, this
change will be accompanied by a reduction in the density of the iron, and
a corresponding increase in dimensions. This phenomenon
5
is termed the growth of cast irons, and irons for high-temperture service
must be in a fully graphtitised state before being put into use.
e) The rate of cooling on the structure of cast iron. A high rate of cooling
during solidification tends to prevent the decomposition of cementite in
an iron which, on slow cooling, would become graphitic. This effect is
important in connection with the choice of a suitable iron for the
production of castings of thin section. Supposing an iron which, when
cooled slowly, had a fine grey structure containing small flakes of
graphite were chosen for such a purpose. In thin sections it would cool so
rapidly that decomposition of the cementite could not take place, and a
thin section of completely white iron would result. Such a section would
be brittle and useless.]This effect is illustrated by casting a "stepped bar"
of iron of a suitable composition. Here, the thin "steps" have cooled so
quickly that no decomposition of the cementite has occurred, as indicated
by the white fracture and the high Brinell figures. The thicker steps,
having cooled more slowly, are graphitic and consequently softer. Due to
the chilling effect exerted by the mould, most castings have a hard white
skin on the surface. This is often noticeable when taking the first "cut" in
a machining operation.
In casting thin sections, then, it is necessary to choose an iron of rather
coarser grey fracture than is required in the finished casting. That is, the
iron must have a higher silicon content than that used for the production
of castings of heavy section.
Carbon can exist in two forms in cast iron, namely as free graphite or
combined with some of the iron to form iron -carbide (ccmentite).
These two varieties are usually referred to as "graphitic carbon" and
"combined carbon" respectively, and the total amount of both types in
the specimen of iron as "total carbon".
This make the casting to be classified as either white or grey.
These terms arise from the appearance of a freshly fractured surface.
Gray iron structure :-

An iron that contains graphite in its structure shows a fracture
surface that is grey and dull in color, as shown in figure 5.
6
Figure 5. Grey cast iron.
Properties and uses of grey cast irons:

These are the most widely used cast irons and they vary in composition
according to specific applications.
Cast irons Cast irons requiring high fluidity are used for very intricate
mouldings for decorative iron work and architectural tracery. They lack
mechanical strength since the high fluidity is obtained by ensuring that the
melt has a high silicon content (2.5-3.5%) and a high phosphorus content
(approximately 1.5%). It is the high phosphorus content which reduces the
strength of the metal.
General-purpose engineering irons have to have reasonable mechanical
strength. Ideally they should have fine graphite flakes in a matrix of pearlite.
Such a cast iron would combine good mechanical properties with good
machinability. The silicon content would be dependent upon the thickness
and mass of the casting, varying between 2.5 % for thin sections and about
1.5% for castings with thick sections. The phosphors content would be kept
low to improve toughness and shock resistance, although up to 0.8% may be
present to improve fluidity. Sulphur must be kept below 0.1 % to avoid
segregation, hard spots and embrittlement.
Local hardening of grey iron castings (e.g. slideways) can be achieved by
chilling. This lone by introducing 'chills' or metal plates into the mould just
behind the surface layer of sand to promote rapid cooling and the formation of
cementite. The hardness occurs only at the surface of the casting and the core
7
remains grey and tough.
Large heavy castings do not require a high silicon content as they

naturally cool slowly and there is adequate time for any cementite to break
down into ferrite and flake graphite. A typical composition would be (1.2-
1.5)% silicon, 0.5% phosphorus and 0.1% sulphur.
White iron structure:-
If, however, the whole of the carbon content of an iron is in the combined
form, as cementite, a fresh fracture surface appears bright and silvery, and
this is termed a white iron structure, as shown in figure 6.
White irons are exception alloy hard, but brittle, it is not often used,
except as the basis for the production of malleable irons, although protions of
many sand casting are made to solidify while, by the insertion of cills in the
sand mould, in order to produce hard and wear resistance surfaces in parts of
the casting.
Figure 6. White cast iron.
Properties and uses of white cast iron :-

White cast irons are little used except as a basis for malleable cast irons
are wear resistant but lack ductility and they break easily since they are very
brittle are virtually un machinable except by grinding.
8
Alloying elements and impurities:

Cast irons are not solely alloys of iron and carbon as the phase equilibrium
diagram would suggest, but complex alloys in which impurities such as
sulphur, phosphorus and alloy elements such as silicon and manganese have a
significant influence on the properties of the casting
1. Silicon
This element is used to soften cast irons by promoting the formation of
flake graphite at the expense of cementite. The silicon content is increased
in irons used for light or thin components which might chill harden by
cooling too quickly in the mould and becoming hard and brittle. The
addition of significant amounts of silicon can reduce the eutectic
composition down to 3.5 % carbon. Thus, at a constant rate of cooling, the
addition of silicon to a cast iron having 3 % carbon will have the
following effects.
Ferritic grey cast iron is produced with 3 per cent silicon.
Ferritic /pearlitic cast iron is produced with 2 per cent silicon.
pearlitic cast iron is produced with 1.5 percent silicon.
White cast iron is produced with no silicon.
Providing sufficient silicon has been added to break down the
cementite into flake graphite (3% silicon in this example) there is no
benefit in adding extra silicon. In fact, the presence of excess silicon will
lead to increased hardness and brittleness.
2. Sulphur
Sulphur is an impurity carried over from the fuel used in the blast
furnace during the extraction of the iron from its ore. The presence of
sulphur in cast irons, even in small quantities, has the effect of stabilising
the cementite and preventing the formation of flake graphite. Thus,
sulphur hardens the cast iron. It also causes embrittlement due to the
formation of iron sulphide (FeS) at the grain boundaries.
3. Manganese
The addition of this element in small quantities is essential in all
ferrous metals as it combines with any residual sulphur present to form
manganese sulphide (MnS). Unlike ferrous sulphide, manganese sulphide
is insoluble in the molten iron and floats to the top of the melt to join the
9
slag. Thus by removing the sulphur, the manganese indirectly softens the
cast iron and also removes a source of embrittlement. Increasing the
manganese content beyond that required to neutralise the sulphur has the
effect of stabilising the cementite and causing hardness in the iron, just as
the sulphur did, but without any embrittlement. Thus it is important to
balance the amount of manganese, sulphur and silicon present with great
care. Manganese also promotes grain refinement and increases the
strength of the cast iron.
4. Phosphorus
Like sulphur, this is a residual impurity from the extraction process. It
is present in cast iron as iron phosphide (Fe 3P). This phosphide forms a
eutectic with ferrite in grey cast irons, and with ferrite and cementite in
white cast irons. Since these eutectics melt at only 950 °C, high
phosphorus content cast irons have great fluidity. Cast irons containing 1
per cent phosphorus are thus very suitable for the production of thin
section castings and highly intricate ornamental castings. Unfortunately
phosphorus, like sulphur, causes hardness and embrittlement in the cast
iron and the amount present must be kept to a minimum in castings where
shock resistance and strength are important.
Types of cast iron

There are several types of cast iron such as :
1) Alloy cast iron
Although complex alloys, such cast irons are still referred to as

common cast ire: the term alloy cast irons being reserved for those cast
irons containing substantial amounts of such metallic elements as
chromium, nickel, etc. Alloying elements may be added to cast irons in
order to improve their properties, and alloy cast irons have been
developed to give high-strength materials, hard and abrasion- resistance
materials, corrosion resistance irons and irons for high-temperature
service.
The alloying elements in cast irons are similar to those in alloy steels,
which are as follows:
 Nickel This is used for grain refinement, to add strength, and to promote
the formation of free graphite. Thus it toughens the casting.
10
 Chromium This stabilises the combined carbon (cementite) present and
thus increases the hardness and wear resistance of the casting. It also
improves the corrosion resistance of the casting, particularly at elevated
temperatures. As in alloy steels, nickel and chromium tend to be used
together because they have certain disadvantages when used separately
which tend to offset their advantages. However, when used together the
disadvantages are overcome, whilst the advantages are retained.
 Copper This is used very sparingly as it is only slightly soluble in iron;
however, it is useful in reducing the effects of atmospheric corrosion.
 Vanadium This is used in heat-resisting castings as it stabilises the
carbides and reduces their tendency to decompose at high temperatures.
 Molybdenum This dissolves in the ferrite and, when used in small
amounts (0.5 % ), it improves the impact strength of the casting. It also
prevents 'decay' at high temperatures in castings containing nickel and
chromium. When molybdenum is added in larger amounts it forms
double carbides, increases the hardness of castings with thick sections,
and also promotes uniformity of the microstructure.
Martensite Martensitic cast irons contain between 4 and 6 % nickel

and approximately 1 per cent chromium, for example, 'Ni-hard' cast
iron. It is naturally martensitic in the cast state but, unlike alloys with
rather less nickel and chromium, it does not need to be quench hardened
thus reducing the possibility of cracking and distortion. It is used for
components which need to resist abrasion. It can only be machined by
grinding.
Austenite Austenitic cast irons contain between 11 and 20 per cent

nickel and up to 5% chromium. These alloys are corrosion resistant, heat
resistant, tough and non magnetic. Since the melting temperatures of
alloy cast irons can be substantially higher than those for common grey
cast irons, care must be taken in the selection of moulding sands and the
preparation of the surfaces of the moulds. Increased venting of the
moulds is also required as the higher temperatures cause more rapid
generation of steam and gases. The furnace and crucible linings must
also be suitable for the higher temperatures and the inevitable increase in
maintenance costs is also a significant factor when working with high-
alloy cast irons.
11
2) Malleable cast iron
Malleable cast irons are produced from white cast irons by a variety
of heat-treatment processes, depending upon the final composition and
structure required. As their name implies, malleable cast irons have
increased malleability and ductility, increased tensile strength, and
increased toughness.
1. Black-heart process
In this process the white iron castings are heated in airtight boxes out
ْ
of contact with air at 850-950 C for 50-170 hours, depending upon the
mass and thickness of the castings. The effect of this prolonged heating
is to break down the iron carbide (cementite) of the white cast iron into
small rosettes of graphite.
The name 'black-heart' comes from the darkened appearance of the
iron, when fractured, resulting from the formation of free graphite.
It is used in the wheel hubs, break drums, conduit fitting control
levers and pedals.
2. White-heart process
In this process the castings are packed into airtight boxes with iron
oxide in the form of high-grade ore. They are then heated to about 1000ْ
C for between 70 and 100 hours, depending upon the mass and thickness
of the castings. The ore oxidises the carbon in the castings and draws it
out, leaving a ferritic structure near the surface and a pearlitic structure
near the centre of the casting. There will also be some fine rosettes of
graphite. White-heart castings behave much as expected of a mild steel
casting, but with the advantage of a very much lower melting point and
higher fluidity at the time of casting.
It is used in the wheel hubs, bicycle and motor cycle frame fittings,
gas, water and steam pipe fittings.
12
3. Pearlitic process
This process is similar to the black-heart process inasmuch as the
castings are heated to 850-950 ْ C for 50-170 hours in a non-oxidising
environment. As in the black-heart process the iron carbide (cementite)
breaks down into austenite and free graphite. However, in the pearlitic
cast iron process, rapid cooling prevents the austenite changing into
ferrite and graphite, and a pearlitic structure is produced instead. Since
this 'pearlitic cast iron' also has a fine grain resulting from the rapid
cooling, it is harder, tougher and has a higher tensile strength than black-
heart cast iron. However, there is a marked reduction in malleability and
ductility. Pearlitic malleable irons can be produced by increasing the
manganese content of the melt from 1.0-1.5 per cent. This inhibits the
production of free graphite and encourages the formation of cementite
and pearlite.
It is used in the gears, couplings, axle housing, differential housing
and components.
Properties and uses of malleable cast irons:
Malleable irons exploit the excellent casting properties of cast iron

during the casting process, after which they are converted by heat-
treatment processes into a composition and structure whose properties
resemble that of a low-carbon steel. This results in castings which are
stronger and much less brittle than ordinary cast irons and are widely
used in the automobile, agricultural machinery and machine tool
industries for the manufacture of small and medium sized stressed
components.
Malleable iron castings are also used in the electrical industry for
conduit fittings, switch gear cases and components.
13
3) Spheroidal graphite cast iron
(Also known as " S.G. cast iron" "nodular iron" or "ductile iron".)
In a normal grey cast iron the graphite flakes are long and thin, and
tend to be pointed at their ends, as shown in figure 7. These long, thin
flakes, having negligible tensile strength, act as discontinuities in the
structure; whilst the sharp-pointed ends of the flakes introduce points of
stress concentration. In S.G. cast iron the graphite flakes are replaced by
spherical particles of graphite (Plate I54A), so that the metallic matrix is
much less broken up, and the sharp "stress raisers" are eliminated.
The formation of this spheroidal graphite is effected by adding small

amounts of cerium or magnesium to the molten iron just before casting.
Since both of these elements have strong carbide-forming tendencies,
the silicon content of the iron must be high enough (at least 2.5%) in
order to prevent the formation, by chilling, of white iron in thin sections.
Magnesium is the more widely used, and is usually added (as a nickel-
magnesium alloy) in amounts sufficient to give a residual magnesium
content of 0.1% in the iron. S.G. cast irons produced by the magnesium
2
process have tensile strengths of up to 775 N/mm .
Figure 7. Speroidal graphite cast iron.
Properties and uses of spheroidal graphite cast irons:

Speroidal graphite cast irons are now used for quite highly stressed
components in the automobile industry. By designing components with
this material in mind, speroidal graphite castings can, in some instances,
replace steel forgings at much lower cost; for example: camshafts,
crankshafts and differential gear carriers for motor vehicles.
14
4) Inoculated cast iron (‫)ﻲﻟﻌﻟا ﻢﻌﻄﻤﻟا ﺮھﺰﻟا ﺪﯾﺪﺣ‬
If an ordinary cast iron is super heated to, say, 1500ْ C before casting,
the formation of graphite is delayed and does not begin until well below
the solidification range. This leads to the production of very small
graphite flakes, which is a desirable feature. Unfortunately, much brittle
cementite is also retained since graphitisation is incomplete under these
conditions of. cooling. Hence the super-heated iron is "inoculated" with
some refractory material which will produce many small particles or
nuclei, wlich, in turn, will promote the formation of fine graphite flakes.
"Meehanite" (a registered proprietary name) is an iron which would
normally solidify "white" but which has been inoculated with calcium
silicide just before casting. Ferrosilicon, graphite and various commercial
inoculants are used in other "trademarked" cast irons. In all of these
products improved mechanical properties are obtained as a result of the
small-flaked graphite induced by inoculation.
15
Alloy Steels
Introduction :
Steels are, essentially, alloys of iron and carbon, containing up to 1.5 % of
carbon. Steel is made by oxidizing away the impurities that are present in the
iron produced in the blast furnace.
The earliest attempt to produce an alloy steel was in 1822 and it has
progressing in producing the alloy steel because of using alloy steel in those
industries upon modern civilization largely depends.
Pure metal objects are used where good electrical conductivity, good
thermal conductivity, good corrosion resistance or a combination of these
properties are required. Therefore alloys are mainly used for structural
materials since they can be formulated to give superior mechanical
properties.
It is called as alloy steel because there are other elements added to the iron
beside the carbon with specific amount for each element. These elements
improve the properties of the alloying steel and make it used with
applications more than the carbon steel. So the most used elements with the
alloy steel and with their amount as a percentage of :
- 2 % Manganese (Mn)
- 0.5 % Chrome (Cr) or Nickel (Ni)
- 0.3 % Tungsten (W) or Cobalt
- 0.1 % Molybdenum (Mo) or Vanadium
- different amount of Aluminum (Al), Copper (Cu) and Silicon (Si).
Alloys steels are generally classified into two major types depending on
the structural classification :
- Low alloy steels :

It is one that possesses similar microstructure to, and requires similar heat
treatment to, plain carbon steels. These generally contain up to 3 – 4 % of one
or more alloying elements for purpose of increasing strength, toughness and
hardenability. The applications of low alloy steels are similar to those of plain
carbon steels of similar carbon contents. Low alloy steels containing nickel
are particularly suitable for applications requiring resistance to fatigue.
- High alloy steels :

Those steels that possess structures, and require heat treatments, that
differ considerably form those of plain carbon steels. A few examples of high
alloy steels are given below:
1. High-speed tool steels
Tungsten and chromium form very hard and stable carbides. Both
elements also raise the critical temperatures and, also, cause an increase in
softening temperatures. High carbon steels rich in these elements provide
hard wearing metal-cutting tools, which retain their high hardness at
temperature up to 600˚C. a widely used high-speed tool steel composition is
containing 18% of tungsten, 4% of chromium, 1% of vanadium and 0.8% of
carbon .
This high-alloy content martensite dose not soften appreciably unit it is
heated at temperatures is excess of 600˚C making them usable as cutting
tools at high cutting speeds.
2. Stainless steels
When chromium is present in amounts in excess of 12% , the steel
becomes highly resistance to corrosion, owing to protective film of chromium
oxide that forms on the metal surface. Chromium also raises the α to γ
transformation temperature of iron, and tends to stabilize ferrite in the
structure.
2
There are several types of stainless steels, and these are summarized below:
a) Ferritic stainless steels contain between 12- 25% of chromium and

less than 0.1% of carbon.
b) Martensitic stainless steels contain between 12-18 % of chromium,
together with carbon contents ranging from 0.1 to 1.5 %
c) Austenitic steels contain both chromium and nickel. When nickel is
present, the tendency of nickel to lower the critical temperatures over-
rides the opposite effect of chromium, and the structure may become
wholly austenitic.
3. Maraging steels
These are very high-strength materials that can be hardened to give
2
tensile strengths up to 1900 MN/m . They contain 18% of nickel, 7% of
cobalt and small amounts of other elements such as titanium, and the carbon
content is low, generally less than 0.05% .
A major advantage of marging steels is that after the solution treatment they
are soft enough to be worked and machined with comparative ease.
Alloy elements cab be classified depending on the using of the alloy (its
application) or according to the basic influence of the element on the alloy
steel properties as follow:
1. alloying elements tend to make carbides such as Cr, W, Ti, V and
Mo it is used in the applications that needs to higher hardness.
2. alloying elements due to analyzing carbides such as Ni, Al, Co and

Si.
Si&Co
Fe3C 3Fe  C 
3. alloying elements stabilizing uestinet γ such as Ni, Co, Cu and Mn.
4. alloy elements stabilizing ferret α such as Cr, W, V, AL and Si.
3
The principal effects which these alloying elements have on the
microstructure and properties of a steel can be classified as follows:
1. The Effect on the Allotropic Transformation Temperatures.
Some elements, notably nickel, manganese, cobalt and copper, raise the
A4 temperature and lower the A3 temperature, as shown in figure 1. In this
way these elements, when added to a carbon steel, tend to stabilise austenite
(γ) and increase the range of temperature over which austenite can exist as a
stable phase.
°/o ALLOYING ELEMENT
Figure 1.—Relative Effects of the Addition of an Alloying Element on the Allotropic

Transformation Temperatures at A3 and A4 which tending to stabilise y.
Other elements, the most important of which include chromium, tungsten,

vanadium, molybdenum, aluminum and silicon, have the reverse effect, in
that they tend to stabilize ferrite (α) by raising the A3 temperature and
lowering the A4 , as indicated in figure 2.
4
°/o ALLOYING ELEMENT
Figure 2. Relative Effects of the Addition of an Alloying Element on the Allotropic Transformation
Temperatures at A3 and A4 tending to stabilize α.
2. The Effect on the Stability of the Carbides.
Some of the alloying elements form very stable carbides when added to a
plain carbon steel. This generally has a hardening effect on the steel,
particularly when the carbides formed are harder than iron carbide itself.
Such elements include chromium, tungsten, vanadium, molybdenum,
titanium and manganese [ these elements are called the carbide stabilizer].
When more than one of these elements are present, a structure containing
complex carbides is often formed.
3. The effect on grain growth.
The rate of crystal growth is accelerated, particularly at high

temperatures, by the presence of some elements, notably chromium.
Fortunately, grain growth is retarded by other elements, notably nickel
and vanadium, whose presence-thus produce a steel which is less sensitive to
the temperature conditions of heat-treatment.
5
4.The Displacement of the Eutectoid Point.
The addition of an alloying element to carbon steel displaces the

eutectoid point towards the left of the equilibrium diagram. That is, a steel
can be completely pearlitic even though it contains less than 0.83% carbon.
For example, the addition of 2.5% manganese to a steel containing 0.65%
carbon produces a completely pearlitic structure in the normalized condition
Figure 3. The Effects of Manganese and Titanium on the Displacement of the Eutectoid Point in
Steel.
Similarly, although a high-speed steel may contain only 0.7% carbon, its
microstructure exhibits masses of free carbide due to the displacement of the
eutectoid point far to the left by the effects of the alloying elements which
are present. Whilst Figure 4. shows the extent to which some elements raise
or lower the eutectoid temperature. This latter will move in sympathy with
the A3 point.
6
Figure 4. The effect of alloying elements on the eutectoid temperature.
5. The Retardation of Transformation Rates.

By adding alloying elements, we reduce the critical cooling rate which is
necessary for the transformation of austenite to martensite to take place. This
feature of the alloying of steels has obvious advantages and all alloying
elements, with the exception of cobalt, will reduce transformation rates.
In order to obtain a completely martensitic structure in the case of a plain
0.83% carbon steel, we must cool it from above 723˚ C to room temperature
in approximately one second. This treatment involves a very drastic quench,
generally leading to distortion or cracking of the component. By adding
small amounts of suitable alloying elements, such as nickel and chromium,
we reduce this critical cooling rate to such an extent that a less drastic oil-
quench is rapid enough to produce a totally martensitic structure. Further
increases in the amounts of alloying elements will so reduce the rate of
transformation that such a steel can be hardened by cooling in air.
7
"Air-hardening" steels have the particular advantage that
comparatively little distortion is produced during hardening. This feature of
alloying is one of the greatest significance.
6. The Improvement in Corrosion-resistance.
The corrosion-resistance of steels is substantially improved by the

addition of elements such as aluminum, silicon and chromium. These
elements form thin but dense and adherent oxide films which protect the
surface of the steel from further attack.
7. Effects on the Mechanical Properties.
One of the main reasons for alloying is to effect improvements in the

mechanical proper ties of a steel. These improvements are generally the
result of physical changes already referred to.
For example:
hardness is increased by stabilising the carbides; strength is increased when

alloying elements dissolve in the ferrite; and toughness is improved due to
refinement of grain.
Some alloying elements may improve the magnetic properties such as
cobalt and tungsten while other elements can made the alloy steel without
any particles such as vanadium.
Some general effects of adding an alloying elements is shown in table 1:
8
Nickel Steel
Nickel is extensively used in alloy steels for engineering purposes,

generally in quantities up to about 5.0%. When so used, its purpose is to
increase tensile strength and toughness. It is also used in stainless steel. The
main sources of nickel are the Sudbury mines in Northern Ontario, Canada;
Cuba and the one-time cannibal island of New Caledonia in the Pacific.
The addition of nickel to a plain carbon steel tends to stabilize the

austenite phase over an increasing temperature range, by raising the A4 point
and lowering the A3 point. Thus, the addition of 25% nickel to pure iron
renders it austenitic, and so non-magnetic, even after slow cooling to room
temperature. The structure obtained after slow cooling to room temperature
can be estimated for a nickel steel of known composition by referring to the
type of diagram devised by Guillet (Figure 5). These diagrams show the
approximate relationship between microstructure, carbon content and the
amount of alloying element added.
Figure 5. The Effects of Nickel as an Alloying Element of the Guillet diagram.
9
At the same time nickel makes the carbides unstable and tends to cause
them to decompose to graphite. For this reason it is inadvisable to add nickel
by itself to a high-carbon steel, and most nickel steels are low-carbon steels.
If a higher carbon content is desired, then the manganese content is usually
increased, since manganese acts as a stabiliser of carbides.
In addition to improving tensile strength and toughness, nickel has a

grain-refining effect which makes the low-nickel, low-carbon steels very
suitable for case-hardening, since grain growth will be limited during the
prolonged period of heating in the region of 900˚ C.
The 3% and 5% nickel steels are the most widely employed. Those with
the lower carbon contents are used mainly for case-hardening, whilst those
with up to 0.4% carbon are used for structural purposes, shafting, gears, etc.
Chromium steels
The main producers of chromium are the South Africa, the Philippines,
Jugoslavia, New Caledonia, Rhodesia, Cuba and Turkey, though not all of
these countries are important exporters. Sierra Leone, a relatively small
producer, is at present expanding its output.
The main function of chromium when added in relatively small amounts
to a carbon steel is to cause a considerable increase in hardness. At the same
time strength is raised with some loss in Ductility, though this is not
noticeable when less than 1.0% chromium is added. The increase in hardness
is due mainly to the fact that chromium is a carbide stabiliser, and forms the
hard carbides Cr7C3 or Cr23C6.
Chromium lowers the A4 temperature and raises the A3 temperature,

forming the closed γ-loop already mentioned. In this way it stabilises the α-
phase at the expense of the γ-phase. The latter is eliminated entirely, as
shown in Figure 6, if more than 11% chromium is added to pure iron, though
with carbon steels a greater amount of
chromium would be necessary to have this effect.
10
Figure 6. The Effects of Chromium as an Alloying Element.
The main disadvantage in the use of chromium as an alloying element is

its tendency to promote grain growth, with the attendant brittleness that this
involves. Care must therefore be taken to avoid overheating or .holding for
too long at the normal heat-treatment temperature.
Steels containing small amounts of chromium and up to 0.45% carbon are

used for axle shafts, connecting-rods and gears; whilst those containing more
than 1.0% carbon are extremely hard and are useful for the manufacture of
ball-bearings, drawing dies and parts for grinding machines.
Chromium is also added in larger amounts up to 21% and has a

pronounced effect in improving corrosion - resistance due to the protective
layer of oxide formed. This oxide layer is extremely thin, and these steels
take a very high polish. They contain little or no carbon and are therefore
completely ferritic and non-hardening (except by cold-work). They are used
widely in the chemical- engineering industry; for domestic purposes, such as
stainless-steel sinks; and in food containers, refrigerator parts, beer barrels,
cutlery and table-ware. The best-known alloy in this group is "stainless
iron", containing 13% chromium and usually less than 0.05% carbon.
11
If the carbon content exceeds 0.1% the alloy is a true stainless steel and
is amenable to hardening by heat treatment. The most common alloy in this
group contains 13% chromium and approximately 0.3% carbon. Due to
displacement of the eutectoid point to the left, this steel is of approximately
eutectoid composition. It is widely used in stainless-steel knives.
Nickel - Chromium Steels

Certain disadvantages attend the addition of either nickel or chromium,
singly, to a carbon steel. Whilst nickel tends to prevent grain growth during
heat-treatment, chromium accelerates it, producing
the attendant brittleness under shock. On the other hand, whilst chromium
tends to form stable carbides, making it possible to produce high-chromium,
high-carbon steels, nickel has the reverse effect in assisting graphitisation.
The deleterious effects of each element can be overcome, therefore, if we
add them in conjunction with each other. Then, the tendency of chromium to
cause grain growth is nullified by the grain-refining effect of the nickel,
whilst the tendency of nickel to favor graphitisation of the carbides is
counteracted by the strong carbide-forming tendency of the chromium.
At the same time other physical effects of each element are additive, so
that they combine in:
- increasing strength,
- corrosion-resistance
- the retardation of transformation rates during heat-treatment.
- heat resistance
- increase and stablies of carbides that leads to increase in the hardness.
- making the drastic water-quenches avoidable.
12
These advantages make the Ni – Cr steels used at very important
fields such as : stations of electricity generation, the tools of surgery , valves,
the tools of cooking and it is etc.
13
Metal Cutting
Introduction :
Before the middle of the 18th century the main material used in
engineering structures was wood. The lathe and a few other machine tools
existed, mostly constructed and most commonly used for shaping wooden
parts. The boring of cannon and the production of metal screws and small
instrument parts were the exceptions. It was the steam engine, with its
requirement of large metal cylinders and other parts of unprecedented
dimensional accuracy, which led to the first major developments in metal
cutting.
The materials of which the first steam engines were constructed were not
very difficult to machine. Grey cast iron, wrought iron, brass and bronze
were readily cut using hardened carbon steel tools, The methods of heat
treatment of tool steel had been evolved by centuries of craftsmen, and
reasonably reliable tools were available. Although rapid failure of the tools
could be avoided only by cutting very slowly.
The technology of metal cutting has been improved by contributions from
all the branches of industry with an interest in machining. The replacement
of carbon tool steel by high speed steels and cemented carbides has allowed
cutting speeds to be increased by many times. Machine tool manufacturers
have developed machines capable of making full use of the new tool
materials, while automatic machines, numerically controlled (NC) machines,
often with computer control (CNC), and transfer machines greatly increase
the output per worker employed. Tool designers and machinists have
optimized the shapes of tools to give long tool life at high cutting speed.
Lubricant manufacturers have developed many new coolants and lubricants
to improve surface finish and permit increased rates of metal removal.
Progress in technology of machining is achieved by the ingenuity and
experiment, logical thought and dogged worrying of many thousands of
practitioners engaged in the many-sided arts of metal cutting. The worker
operating the machine, the tool designer, the lubrication engineer, the
metallurgist, are all constantly probing to find answers to new problems
created by the necessity to machine novel materials, and by the incentives to
reduce costs, by increasing rates of metal removal, and to achieve greater
precision or improved surface finish.
During cutting, the interface between tool and work material is largely
inaccessible to observation, but indirect evidence concerning stresses,
temperatures, metal flow and interactions between tool and work material
While heat can be made to fuse and unite, it can also be employed to
separate, that is, perform a cutting operation. The earliest arc welding patent
for the Benardos carbon-arc process also mention cutting. This was achieved
by forming a molten pool and allowing it to fall out by gravity.
The results or thermal cutting in this way are rough and generally
unsatisfactory bur great improvements result from combining the heat source
with a jet of gas, usually oxygen or air.
 An air jet with a carbon arc is widely used for gouging the surface of
steel. The arc melts a pool on the surface and the air jet blows it away.
 An oxygen jet with an oxy-acetylene heat source was the most
commonly used thermal cutting process for steel. Although today oxy-
propane has become widely used.
 In plasma cutting an inert gas tungsten arc is constricted by making the
arc pass through a water-cooled nozzle and the inert gas thus
concentrated forms the jet which elects the molten metal from the cut.
 A recent development has allowed air to be used the plasma torch for
cutting thin sheet steel. This has only been possible by finding an
electrode material more resistant to oxidation than tungsten.
Most cutting processes, including oxy-fuel gas cutting, are available

with computer controlled profiling equipment which can access standard
shapes in memory and select the sequence of cutting and the arrangement
of shapes to provide the most economical use of material.
٢
There are different types of metal cutting process, we will study the
following three types as an example of the materials used for cutting:
1) Cutting with the oxy-fuel gas

The oxy-fuel gas cutting process depends on the reaction between
oxygen and iron to form iron oxides. This reaction gives out
considerable heat and is self-sustaining once the required preheat or
'kindling' temperature is reached. To earn out cutting a blowpipe is
needed in which the nozzle supplying the oxy-fuel gas flame contains a
central ounce through which a jet of oxygen can be directed. Actually
the preheating flame is usually supported from a ring of holes as shown
in figure 1.
Figure 1. Principle of oxy-fuel gas cutting.
Cutting then commences with the flow of oxygen sweeping away

the fluid products of combustion through the slot which is being cut.
The slot is called a kerf. Oxy-fuel gas cutting is sensitive to the
cleanliness of the surface being cut and if possible rust or paint should
be removed before cutting begins.
Manual oxy-fuel gas cutting is extremely useful for reclaiming
scrap metal and fettling castings, etc. Although manual cutting is used
on a small scale for preparing edges for welding the quality of the cut is
greatly improved by mechanisation. A major use of oxy-fuel gas
cutting is in mechanised or automated cutting.
٣
2) Laser cutting
Laser cutting was the first and still is the most important application
for CO2 lasers up to 500W. It is normally carried out with the aid of a
gas jet,. as shown in figure 2, oxygen or compressed air being used for
ferrous materials (as the resultant exothermic reaction assists the cutting
process) and inert gases when cutting non-metals. The process will cut
profiles with precision at high speed and is especially suitable for heat
resisting and alloy steels which are difficult to cut by other means.
For example: Cutting speeds for mild steel with a 500 \V laser are
indicated by the rule-of-thumb:
in 40 80 120 160
Steel thickness mm 1 2 3 4
1000
Cutting speed m/min 4 3 2 1 ipm 160 120 80 40
Figure 2. Principle of laser cutting.
٤
3) some materials used for cutting such as diamond which is the

hardest of all materials, diamond, has long been employed as a cutting
tool although its high cost has restricted use to operations where other
tool material cannot perform effectively. Diamond tools show a much
lower rate of wear and longer tool life than carbides or oxides under
conditions where abrasion is the dominant wear mechanism because
of their very high hardness. The extreme hardness of diamond is
related to its crystal structure. This consists two interpenetrating, face-
centered cubic lattices arranged so that each carbon atom has four near
neighbors to which it is attracted by covalent bonds.
Importance of Coolants and lubricants in cutting of materials:

A tour of most machine shops will demonstrate that some cutting
operations are carried out dry, but in many other cases, a flood of liquid is
directed over the tool, to act as a coolant and or a lubricant. These cutting
fluids perform a very important role and many operations cannot be
efficiently carried out without the correct type of fluid. They are used for a
number of objectives:
(1) To prevent the tool, work piece and machine from overheating.
(2) To increase tool life.
(3) To improve surface finish.
(4) To help clear the swarf from the cutting area.
٥
Non–Ferrous Materials
Introduction :
The non-ferrous metals which are most commonly used by engineers, it also
refers to the 38 metals other than iron that are known to man.
Two of the most important non-ferrous metals are Aluminum (Al) and
Copper (Cu). They are not only form the bases of many important alloys, but
they are widely used in their own right as pure metals.
A list of non-ferrous metals would be complete without mention of the
'new metals' . Although known for many years, these metals have only been
available in bulk for engineering applications since the Second World Ware.
Further with the development of supersonic aircraft and the nuclear power
industry, that there has been a large – scale commercial demand for these
materials.
These 'new metals' are very expensive compared with the more
conventional engineering materials and they are only used where their special
properties can be fully exploited.
The pure non-ferrous metals are used mainly where their properties of
corrosion resistance and high electrical and thermal conductivity can be
exploited. They are not widely used as structural materials in mechanical
engineering because of their relatively low strengths.
Aluminum and Its Alloys

Introduction :
The first samples of aluminum was produced in 1825 by the Danish
physicist and chemist H.C. Oersted.
While in 1886 a C.M. Hall had discovered a relatively cheap method for
producing aluminum by electrolyzing a fused mixture of aluminum oxide and
the mineral cryolite.
Aluminum cannot be purified by blowing air through it, as in the case of
iron. This treatment would oxidise the aluminum and leave behind the
impurities. Therefore the ore must be purified before being electrolysed, and
this, involves an expensive chemical process. Although aluminum has a great
affinity for oxygen, its corrosion-resistance is relatively, high. This is due to
the dense impervious film of oxide which forms on the surface of the metal
and protects it from further oxidation. The high affinity of aluminum for
oxygen also makes it useful as a deoxidant in steels and also in the Thermit
process of welding.
The properties of aluminum which chiefly affect its use as a metallurgical
material are its low relative density and its high affinity for oxygen. Since its
relative density is only about one-third that of steel, or of a copper-base alloy,
it is used, when alloyed with small amounts of other elements, for castings in
aero, automobile and constructional engineering. Moreover, alloying and heat-
treatment can produce alloys of aluminum which are, weight for weight,
stronger than steel, so that the use of aluminum alloys is further extended to
stress-bearing members in both aero-engine and air-frame.
The fact that aluminum has over 50% of the specific conductivity of copper
means that, weight for weight, it is a better conductor of electricity than is
copper. Hence it is now widely used, generally twisted round a steel core for
strength, as a current carrier in the electric "grid" system. Pure aluminum is
2
relatively soft and weak (it has a tensile strength of about 90 N/mm in the
annealed condition), so that for most other engineering purposes it is used in
the alloyed condition.
2
Alloys of Aluminum
The addition of alloying elements is made principally to improve
mechanical properties, such as tensile strength, hardness, rigidity and
machinability, and sometimes to improve fluidity and other casting properties.
One of the chief-.defects to which aluminum alloys are prone is porosity

<
due to gases dissolved during the melting process. Molten Aluminum will
dissolve considerable amounts of hydrogen if, for any reason, this is present in
the furnace atmosphere. When the metal is cast and begins to solidify the
solubility of hydrogen diminishes almost to zero, so that tiny bubbles of gas
are formed in the partly solid metal. These cannot escape, and give rise to
"pinhole" porosity. The defect is eliminated by treating the molten metal
before casting with a suitable "flux, or by bubbling nitrogen or chlorine
through the melt. As a substitute for chlorine, which is a poisonous gas, tablets
of the organic compound hexachlorethane can be used.
Aluminum alloys are used in both the cast and wrought conditions. Whilst
the mechanical properties of many of them, both cast and wrought, can be
improved by the process known as "precipitation-hardening", a number are
used without any such treatment being applied. It is convenient, therefore, to
classify the somewhat bewildering multitude of aluminum alloys into the
following two main groups, according to the condition in which they are
employed.
1. Wrought Alloys
a) Wrought alloys which are not heat – treated:
The main requirements of alloys in this group are sufficient strength and
rigidity in the work-hardened state, coupled with good Son-resistance. As
will be seen, these alloys are widely used in the manufacture of panels for
land-transport vehicles. Here the high corrosion – resistance of the
aluminum - magnesium alloys is utilized, those with a higher magnesium
value having an excellent resistance to sea-water and marine atmospheres,
so that they are used extensively for marine super - structures. The desired
mechanical properties are produced by the degree of cold-work applied in
the final cold-working operation and these alloys are commonly supplied
as "soft", "quarter hard" , "half hard", "three-quarter hard" or "full hard".
The main disadvantage is that,
3
once the material has been finished to size, no further variation can made in
mechanical properties (other than softening by annealing), whereas, with
the precipitation-hardening alloys, the properties can be varied, within
limits, by heat-treatment.
b) Wrought alloy which are heat – treated:

The most significant feature of the aluminum alloys is the ability of
some of them to undergo a change in properties under suitable heat-
treatment. Although this phenomenon is not confined to aluminum
alloys, but is possible with any alloy in a series in which change in
solubility of some constituent in the parent metal takes place, it is
more widely used in the aluminum-base alloys than in any others.
The phenomenon was first observed by a German research metal-
lurgist, Dr. Alfred Wilm, in 1906, who noticed that an aluminum alloy
containing small amounts of magnesium, silicon and copper, when
quenched from a temperature in the region of 500˚ C, subsequently
hardened unassisted, if allowed to remain at room temperature over a
period of days.
The strength increased in this way, reaching a maximum value in just
under a week, and the effect was subsequently known as " age-
hardening". About four years later Wilm transferred the sole rights of
his patent to the Durener Metal Works at Duren in Western Germany, and
the alloy produced was named "duralumin" .
The first significant use of duralumin was during the First World War,
when it found application in the structural members of the airships bearing
the name" of Graf von Zeppelin.
The age-hardening process can be accelerated by heating the quenched
alloy at temperatures up to 180˚ C. Such treatment was referred to
originally as "artificial age-hardening", but both of these lightly
misleading titles are now covered in modern metallurgical nomenclature by
the general term "precipitation-hardening".
We will consider the application of this principle to the precipitation-

hardening of aluminum-copper alloys.
4
.
Let us assume that we have an aluminum-copper alloy containing 4 0
% copper. At temperatures above 500˚ C this will consist entirely of a solid
solution as indicated by the equilibrium diagram figure 1. If we now allow
the alloy to cool very slowly to room temperature, equilibrium will be
reached at each stage and particles of the inter metallic compound CuAl2
(θ) will form as a non-coherent precipitate. This precipitation will
commence at A and continue until at room temperature only 0.2% (X)
copper remains in solution in the aluminum. The resulting structure will
lack strength because only 0.2% copper is left in solution, and it will be
brittle because of the presence of coarse particles of CuAl2.
Figure 1. Aluminum-rich end of the Aluminum-Cooper equilibrium

diagram, showing the observed microstructure effects of slow cooling and
precipitation-hardening.
If the alloy is now slowly reheated, the particles of CuAl2 will be

gradually absorbed, until at A we once more have a complete solid solution
a ( in industrial practice a slightly higher temperature, B, will
5
be used to ensure complete solution of the CuAl2). On quenching the alloy
we retain the copper in solution, and, in fact, produce a supersaturated
solution of copper in aluminum at room temperature.
In this condition the alloy is somewhat stronger and harder because
there is more copper actually in solid solution in the aluminum, and it
is also much more ductile, because the brittle particles of CuAl2
are now absent. So far these phenomena permit of a straightforward
explanation, forthcoming from a simple study of the microstructure. What
happens subsequently is of a sub-microscopical nature, that is, its
observation is beyond the range of an ordinary optical microscope.
If the quenched alloy is allowed to remain at room tempera-> it will be
found that strength and hardness gradually increase (with corresponding
reduction in ductility) and reach a maximum in about six days. After this
time has elapsed no further appreciable changes occur in the properties. The
completely α-phase structure obtained by quenching is not the equilibrium
structure at room temperature. It is in fact super-saturated with copper so
that there is a strong urge for copper to be rejected from the solid solution α
as particles of the non-coherent precipitate CuAl2 (θ). This stage is never
actually reached at room temperature because of the sluggishness of
diffusion bf the copper atoms within the aluminum lattice. However, some
movement does occur and the copper atoms take up positions within the
aluminum lattice so that nuclei of the intermediate phase (θ') are formed.
These nuclei are present as a coherent precipitate continuous with the
original a lattice, and in this form, cause distortion within the α lattice. This
effectively hinders the movement of dislocations and so the yield strength is
increased. The sub-microscopical change within the structure can be
represented so:
Cu + 2Al θ'
[Al lattice] [Al lattice] [Intermediate coherent precipitate]
An improvement in properties over those obtained by ordinary "natural

age-hardening" can be attained by "tempering" the quenched alloy at
temperatures up to nearly 200˚ C for short periods. This treatment increases
the amount of the intermediate coherent precipitate θ' by accelerating the
rate of diffusion, and so strength and hardness of the alloy rise still further.
If the alloy is heated to a higher temperature, a stage is reached where the
structure begins to revert
6
rapidly to one of equilibrium and the coherent intermediate phase θ'
precipitates fully as non-coherent particles of θ (CuAl2):
θ' θ
[Intermediate coherent precipitate] [Non-coherent precipitate CuAl2 ]
When this occurs both strength and hardness begin to fall. Further
increases in temperature will cause the θ particles to grow to a size making
them easily visible with an ordinary optical microscope, and this will be
accompanied by a progressive deterioration in mechanical properties.
Figure 2 illustrates the general effects of variations in time and temperature
during post-quenching treatment for a typical alloy of | the precipitation-
hardening variety. At room temperature (20˚ C) the tensile strength
increases slowly and reaches a maximum of about
2
390 N/mm . Precipitation-treatment at temperatures above 100° C will
result in a much higher maximum tensile strength being reached.
Optimum strength is obtained by Treatment at 165˚ C for about
ten hours, after which, if the treatment time is prolonged, rapid
precipitation of non-coherent particles of θ (CuAl2) will cause a
deterioration in tensile strength and hardness as shown by curve C.
Treatment at 200˚ C, as represented by curve D , will give poor results
because the rejection from solution of non-coherent θ is very rapid
such that precipitation will ''overtake" any increase in tensile strength. This
process of deterioration in structure and properties due to faulty heat-
treatment is generally termed "reversion". Time and temperature of
precipitation-treatment differ with the composition of the alloy, and must
always be controlled accurately to give optimum results.
7
Figure 2. The effects of time and temperature of participation –

treatment on the structure and tensile strength of a suitable alloy.
There are a number of alloy compositions sold under the general trade
name of "Duralumin", but all of them rely on the presence of
approximately 4.0% copper to effect hardening. In addition, both
Magnesium and silicon are usually present, so that hardening will to some
extent be assisted by the formation of Mg2Si. Thus, one standard grade of
duralumin contains 4.0% copper, 0.6% manganese, 0.5% magnesium and
0.4% silicon, with small amounts of iron. The main function of manganese
is to refine the grain.
Just as " tempering " will accelerate precipitation-hardening, so will
refrigeration impede the process. This fact was utilised extensively in
aircraft production during the Second World War. If a duralumin rivet is
solution-treated it is in a soft condition, but if sufficient time is allowed to
elapse before using the solution-treated rivet it will begin to harden and will
possibly split whilst being driven. It was found that if, immediately after
quenching, the duralumin rivets were stored in a refrigerator at about —20°
C, precipitation-hardening was considerably slowed down, and the rivets
could therefore be stored at the sub-zero temperature until they were
required.
Although the addition of copper forms the basis of many of the
precipitation-hardening aluminum alloys, copper is absent from a number
of them which rely instead on the presence of magnesium
8
and silicon. Such alloys have a high electrical conductivity approaching that
of pure aluminum, so that they can be used for the manufacture of
overhead, conductors of electricity. Most commercial grades of aluminum
contain iron as an impurity, but in some of these alloys it is Utilised in
greater amounts in order to increase strength by promoting the formation of
FeAl3, which assists in precipitation-hardening. Titanium finds application
as a grain refiner, whilst other alloys con-taining zinc and chromium
produce tensile strengths in excess of
2
620 N/mm in the heat-treated condition.
2. Casting Alloys
a) Cast alloys which are not heat-treatment
This group of alloys contain those which are widely used as general-
purpose materials as sand-casting. These alloys are mainly used when rigidity,
fluidity in casting and good corrosion-resistance are important than strength.
Undoubtedly the most widely used alloys in this class are those containing
between 9 and 13 % silicon, with occasionally small amounts of copper.
b) Cast alloys which are heat-treatment

Many of these alloys are of the 4 % copper type, whilst others contain an
addition of about 2 % nickel. Precipitation-hardening is then due to the
combined effects of intermediate phases based on the intermetallic
compounds CuAl2 and NiAl3 .
As a cast alloy it is used where high strength is required at elevated
temperatures, as, for example, in high duty piston and cylinder heads.
9
Copper and Its Alloys

Introduction :
Copper was undoubtedly the first metal to be used by Man. In many
countries it is found in small quantities in the metallic state and, being soft, it
was readily shaped into ornaments and utensils.
It is thought that bronze was accidentally produced in Cornwall by smelting
ores containing both tin- and copper-bearing minerals in the camp fires of
ancient Britons. It was the best material for making knives and other cutting
implements.
Properties and Uses of Copper
A very large part of the world's production of metallic copper is used in the
unalloyed form, mainly in the electrical industries. Copper has a very high
specific conductivity, and is, in this respect, second only to silver, to which it is
but little inferior. When relative costs are considered, copper is naturally the
metal used for industrial purposes demanding high electrical conductivity.
1) The Electrical Conductivity of Copper.

The International Standard of Electrical Resistance for annealed copper was
adopted in 19137 and copper which reached this standard
was said to be 100% conductive. The fact that, working to the 1913 standard,
figures of 101 and 102% are frequently quoted is explained by reason of
improvements that have taken place in the production of copper since 1913.
As indicated in Figure 3, the presence of impurities reduces electrical

conductivity. To a less degree, cold-work has the same effect. Reduction in
conductivity caused by the presence of some elements in small amounts is not
great, so that up to 1% cadmium, for example, is added to telephone wires in
order to strengthen them. Such an alloy, when hard-drawn, has a tensile
2 2
strength of some 460 N/mm as compared with 340 N/mm for hard-drawn,
pure copper, whilst the electrical conductivity is still over 90% of that for soft
pure copper. Other elements have pronounced effects on conductivity; 0.04%
phosphorus, for
10
example, will reduce the electrical conductivity to about 75% of that for pu re
copper.
Figure 3. The Effect of Impurities on the Electrical Conductivity of Copper.
2) The Commercial Grades of Copper

It include both furnace-refined and electrolytically refined metal. High-
conductivity copper (usually referred to as O.F.H.C. or "oxygen-free high
conductivity") is of the highest purity, and contains at least 99-9% copper. It is
used where the highest electrical and thermal conductivities are required, and
is copper which has been refined electrolytically.
Fire-refined ..grades of copper can be either "tough pitch" or "deoxidised"
according to their subsequent application. The former contains small amounts
of oxygen (present as cuprous oxide, Cu2O) absorbed during the
manufacturing process. It is usually present in amounts of the order of 0.04-
0.05% oxygen (equivalent to 0.45- 0.55% cuprous oxide). The cuprous oxide is
present as tiny globules, which are part of a copper-cuprous oxide eutectic.
These globules have a negligible effect as far as electrical conductivity, and
most of the other properties, are concerned.
11
For processes such as welding and tube-making, however, the existence of
these globules is extremely deleterious, since reducing atmospheres containing
hydrogen cause "gassing" of the metal. Hydrogen is soluble in solid copper, so
that it comes into contact with the subcutaneous globules of cuprous oxide,
reducing them thus:
Cu20 + H2 2Cu + H20
Although this is what is called a "reversible reaction", the high
concentration of hydrogen relative to cuprous oxide makes-the reaction
proceed to the right, and the water formed is present as steam, which is
almost insoluble in solid copper. It is therefore precipitated at the crystal
boundaries, thus, in effect, pushing the crystals a part and reducing
the ductility by as much as 85% and the tensile strength by 30 - 40%.
Under the microscope "gassed" tough-pitch copper is recognised by the
thick grain boundaries, which are really minute fissures, and by the absence of
cuprous oxide globules.
For such purposes as welding, therefore, copper is deoxidised before being
cast by the addition of phosphorus, which acts in the same way as the
manganese used in deoxidising steels. A small excess of
phosphorus, of the order of 0-04%, dissolves in the copper after deoxidation,
and this small amount is sufficient to reduce the electrical conductivity by as
much as 25%. So, whilst copper which is destined for welding or thermal
treatment in hydrogen-rich atmospheres should be of this type,
copper deoxidised by phosphorus would be unsuitable for electrical purposes,
where either electrolytic copper or good-quality tough-pitch copper must be
used.
Up to 0.5% arsenic was added to much of the copper used in
the construction of locomotives. This addition considerably increased
the strength at elevated, temperatures by raising the softening temperature from
˚
about 190 C for the pure metal to 550˚ C for arsenical copper. This
made arsenical copper useful in the manufacture of steam locomotive fire-
boxes, boiler tubes and rivets, since the alloy, whilst being stronger at high
temperatures, still had a high thermal conductivity.
The addition of 0.5 % lead or tellurium imparts free-cutting properties to

copper and provides a material which can be machined
12
to close tolerances whilst still retaining 95% of the conductivity of
pure copper.
3) The Effects of Impurities
The Effects of Impurities on the electrical properties of copper have
already been mentioned. Quite small amounts of some impurities will also
cause serious reductions in the mechanical properties.
Bismuth is possibly the worst offender, and even as little as 0-002% will
sometimes cause trouble, since bismuth is insoluble in amounts in excess of
this figure, and, like ferrous sulphide in steel, collects as brittle films at the
crystal boundaries. Antimony produces similar effects and, in particular,
impairs the cold-working properties.
Selenium and tellurium make welding difficult, in addition to re-ducing the
conductivity and cold-working properties; whilst lead causes hot-shortness,
since it is insoluble in copper and is actually molten at the hot-working
temperatures.
The Copper-base Alloys

The copper-base alloys include the brasses and bronzes, the latter being
copper-rich alloys containing either tin, aluminum, silicon or beryllium;
though the tin bronzes are possibly the best known.
☻The Brasses
The brasses comprise the useful alloys of copper and zinc containing up to
45% zinc, and constitute one of the most important groups of non-ferrous
engineering alloys.
As shown by the equilibrium diagram figure 4, copper will dissolve up to
32.5% zinc at the solidus temperature of 902° C, the proportion increasing
to 39.0% at 454° C. With extremely slow rates of cooling, which allow
the alloy to reach structural equilibrium, the solubility of zinc in copper will
again decrease to 35.2% at 250° C. Diffusion is very sluggish, however,
at temperatures below 450° C, and with ordinary industrial rates of cooling
the amount of zinc which can remain in solid solution in copper at room
temperature is about 39 %. The solid solution so formed is represented by
the symbol a. Since this solid solution is of the disordered type, it is prone to
the phenomenon of coring, though this is not extensive, indicated by the
13
narrow range between liquids and solidus.
If the amount of zinc is increased beyond 39 % another phase, β', will
appear in the microstructure of the slowly cooled brass. This phase is hard, but
quite tough at room temperature, and plastic when it changes to its
modification β above 454° C. Further increases in the zinc content beyond
50 % cause the appearance of the phase γ in the structure. This is extremely
brittle, rendering alloys which contain it unsuitable for engineering purposes.
Due to coring effects, an alloy which is nominally α-phase in structure may

contain some β'- phase in the as-cast condition. This will depend upon the
rate of cooling and the nearness of the composition of the alloy to the
 ' phase boundary. Such β'-phase will usually be absorbed
fairly quickly on subsequent mechanical working whilst hot. The
' alloys usually have a Widmanstatten structure on cooling, due to
the manner in which the particles of the α-phase precipitate as the alloy cools
from out of the β-phase area.
As mentioned above, the α-phase is quite soft and ductile at room
temperatures, and for this reason the completely α-phase brasses are excellent
cold-working alloys. The presence of the β'-phase, however, makes them
rather hard and with a low capacity for cold-work; but since the β-phase is
plastic at red heat, the α + β' brasses are best shaped by hot-
working processes, such as forging or extrusion. The a-phase tends to be
rather hot-short within the region of 30% zinc and between the
temperatures of 300 and 750° C, and is therefore much less suitable
as a hot-working alloy unless temperatures and working conditions are
strictly controlled. The α-phase would also introduce difficulties during
the extrusion of the α + β' alloys were it not for the fact that it
is absorbed into the β-phase when the 60-40 composition (one of the most
popular alloys of this group) is heated to a point above the
 phase boundary in the region of 750° C, thus producing a
uniform plastic structure of β -phase only. The α-phase is usually in
process of being precipitated whilst hot-working is taking place, so
that, instead of the Widmanstatten structure being formed again as
the temperature tails, it is replaced by a refined granular α + β'
structure which possesses superior mechanical properties to those of the
directional Widmanstatten structure. The needle-shaped crystals of the α-
phase are prevented from forming by the mechanical disturbances which
14
accompany the working process.
Figure 4. The Copper-Zinc Thermal-equilibrium Diagram.

The lower diagram indicates the relationship between composition
and mechanical Properties.
Thus the brasses can conveniently be classified according to whether they

are hot-working or cold-working alloys.
15
☻The Tin Bronzes
Bronzes containing approximately 10 % Tin were probably the first alloys
to be used by man. One of the significant factors in the early Roman conquests
was undoubtedly the bronze sword, and it is thought that in even earlier times
metal-workers realized that a high Tin content, in the region of 10 % produced
a hard bronze whilst less Tin gave a softer alloy.
16
Polymers & Plastics

Introduction :
Naturally occurring polymers—those derived from plants and animals have
been used for many centuries; these materials include wood, rubber, cotton,
wool, leather, and silk. Other natural polymers such as proteins, enzymes,
starches, and cellulose are important in biological and physiological processes
in plants and animals.
Modern scientific research tools have made possible the determination of
the molecular structures of this group of materials, and the development of
numerous polymers, which are synthesized from small organic molecules.
Many of our useful plastics, rubbers, and fiber materials are synthetic
polymers. In fact, since the conclusion of World War II, the field of materials
has been virtually revolutionized by the advent of synthetic polymers. The
synthetics can be produced inexpensively, and their properties may be managed
to the degree that many are superior to their natural counterparts. In some
applications metal and wood parts have been replaced by plastics, which have
satisfactory properties and may be produced at a lower cost.
To under stand the polymers structure we should see first the Hydrocarbon
Molecules. Since most polymers are organic in origin, we briefly review some
of the basic concepts relating to the structure of their molecules. First, many
organic materials are hydrocarbons; that is, they are composed of hydrogen
and carbon. Furthermore, the intermolecular bonds are covalent. Each carbon
atom has four electrons that may participate in covalent bonding, whereas
every hydrogen atom has only one bonding electron. A single covalent bond
exists when each of the two bonding atoms
contributes one electron, as represented schematically in Figure 1 for a
molecule of methane (CH4). Double and triple bonds between two carbon
atoms involve the sharing of two and three pairs of electrons, respectively.
Figure 1.Schematic representation of covalent bonding in a molecule of methane (CH4).
For example, in ethylene, which has the chemical formula C 2H4, the two
carbon atoms are doubly bonded together, and each is also singly bonded to
two hydrogen atoms, as represented by the structural formula
where ─ and ═ denote single and double covalent bonds, respectively. An

example of a triple bond is found in acetylene, C 2H2:
Molecules that have double and triple covalent bonds are termed
unsaturated. That is, each carbon atom is not bonded to the maximum (four)
other atoms; as such, it is possible for another atom or group of atoms to
become attached to the original molecule. Furthermore, for a saturated
hydrocarbon, all bonds are single ones, and no new atoms may be joined
without the removal of others that are already bonded.
2
Polymer Molecules:
The molecules in polymers are gigantic in comparison to the hydrocarbon
molecules already discussed; because of their size they are often referred to as
macromolecules.
Within each molecule, the atoms are bound together by covalent interatomic
bonds. For carbon chain polymers, the backbone of each chain is a string of
carbon atoms. Many times each carbon atom singly bonds to two adjacent
carbons atoms on either side, represented schematically in two dimensions as
follows:
Each of the two remaining valence electrons for every carbon atom may be
involved in side-bonding with atoms or radicals that are positioned adjacent to
the chain. Of course, both chain and side double bonds are also possible. These
long molecules are composed of structural entities called repeat units, which
are successively repeated along the chain.1 The term monomer refers to the
small molecule from which a polymer is synthesized. Hence, monomer and
repeat unit mean different things, but sometimes the term monomer or
monomer unit is used instead of the more proper term repeat unit.
The Chemistry of Polymer Molecules:

Consider again the hydrocarbon ethylene (C 2H4), which is a gas at ambient
temperature and pressure, and has the following molecular structure:
If the ethylene gas is reacted under appropriate conditions, it will transform

to polyethylene (PE), which is a solid polymeric material. This process begins
when an active center is formed by the reaction between an initiator or catalyst
species ( ) and the ethylene monomer, as follows:
3
Figure 2. For polyethylene, (a) a schematic representation of repeat unit and chain
structures, and (b) a perspective of the molecule, indicating the zigzag backbone structure.
Molecular Structure:
The physical characteristics of a polymer depend not only on its molecular
weight and shape but also on differences in the structure of the molecular
chains. Modern polymer synthesis techniques permit considerable control over
various structural possibilities. This section discusses several molecular
structures including linear, branched, cross linked, and network, in addition to
various isomeric configurations.
4
Circles designate individual repeat units.
Figure 3. Schematic representations of: (a) linear, (b) branched, (c) cross linked, and
(d) network (three-dimensional) molecular structures.
Linear Polymers
They are those in which the repeat units are joined together end to end in
single chains. These long chains are flexible and may be thought of as a mass
of spaghetti, as represented schematically in Figure 3.a, where each circle
represents a repeat unit. For linear polymers, there may be extensive van der
Waals and hydrogen bonding between the chains. Some of the common
polymers that form with linear structures are polyethylene, poly(vinyl
chloride), polystyrene, poly(methacrylate), nylon, and the fluorocarbons.
Branched Polymers
Polymers may be synthesized in which side-branch chains are connected to
the main ones, as indicated schematically in Figure 3.b, these are fittingly
called branched polymers. The branches, considered to be part of the main-
chain molecule, may result from side reactions that occur during the synthesis
of the polymer. The chain packing efficiency is reduced with the formation of
side branches, which results in a lowering of the polymer density. Those
5
polymers that form linear structures may also be branched. For example, high
density polyethylene (HDPE) is primarily a linear polymer, while low density
polyethylene (LDPE) contains short chain branches.
Cross linked Polymers

In cross linked polymers, adjacent linear chains are joined one to another at
various positions by covalent bonds, as represented in Figure 3.c. The process
of cross linking is achieved either during synthesis or by a nonreversible
chemical reaction.
Often, this cross linking is accomplished by additive atoms or molecules
that are covalently bonded to the chains.
Network Polymers
Multifunctional monomers forming three or more active covalent bonds,
make three-dimensional networks (Figure 3.d) and are termed
network polymers. Actually, a polymer that is highly cross linked may also be
classified as a network polymer. These materials have distinctive mechanical
and thermal properties; the epoxies, polyurethanes, and phenol-formaldehyde
belong to this group.
Polymers are not usually of only one distinctive structural type. For
example, a predominantly linear polymer might have limited branching and
cross linking.
General properties of polymeric materials

The properties of polymeric materials can vary widely, but they all have
certain properties in common:
1. Electrical insulation
All polymeric materials exhibit good electrical insulation properties.
However, their usefulness in this field is limited by their low heat
resistance and their softness. Thus they are useless as formers on which to
wind electric radiator elements, and as insulators for use out of doors
where their relatively soft surface would soon be roughened by the
weather. Dirt collecting on this roughened surface would then provide a
conductive path, causing a short circuit.
2. Strength/weight ratio
6
Polymeric materials vary in strength considerably. Some of the
stronger, such as nylon, compare favorably with the weaker metals. All
polymeric materials are much lighter than any of the metals used for
engineering purposes. Therefore, properly chosen and proportioned, their
strength/weight ratio compares favorably with many light alloys and they
are steadily taking over engineering, duties which, until recently, were
considered the prerogative of metal.
3. Corrosion resistance
All polymeric materials are inert to most inorganic chemicals and can
be used in environments which are hostile even to the most corrosion-
resistant metals. The synthetic rubbers, which are a product of polymer
chemistry, are superior to natural (polyisoprene) since they are not
attacked by oils and greases.
Mechanical Behavior of Polymers / Stress–Strain Behavior:

The mechanical properties of polymers are specified with many of the same
parameters that are used for metals that is, modulus of elasticity, and yield and
tensile strengths. For many polymeric materials, the simple stress–strain test is
employed for the characterization of some of these mechanical parameters. The
mechanical characteristics of polymers, for the most part, are highly sensitive
to the rate of deformation (strain rate), the temperature, and the chemical nature
of the environment (the presence of water, oxygen, organic solvents, etc.).
Some modifications of the testing techniques and specimen configurations used
for metals are necessary with polymers, especially for the highly elastic
materials, such as rubbers.
Three typically different types of stress–strain behavior are found for
polymeric materials, as represented in Figure 4. Curve A illustrates the stress–
strain character for a brittle polymer, inasmuch as it fractures while deforming
elastically. The behavior for a plastic material, curve B, is similar to that for
many metallic materials; the initial deformation is elastic, which is followed by
yielding and a region of plastic deformation. Finally, the
deformation displayed by curve C is totally elastic; this rubber-like elasticity
(large recoverable strains produced at low stress levels) is displayed by a class
of polymers termed the elastomers.
7
Figure 4. The stress–strain behavior for brittle (curve A), plastic (curve B), and highly
elastic (elastomeric) (curve C) polymers.
Figure 5. Schematic tensile stress–strain curve for a semicrystalline polymer. Specimen

contours at several stages of deformation are included.
Fracture of Polymers:
8
The fracture strengths of polymeric materials are low relative to those of
metals and ceramics. As a general rule, the mode of fracture in thermosetting
polymers (heavily cross linked networks) is brittle. In simple terms, during the
fracture process, cracks form at regions where there is a localized stress
concentration (i.e., scratches, notches, and sharp flaws). As with metals, the
stress is amplified at the tips of these cracks leading to crack propagation and
fracture. Covalent bonds in the network or cross linked structure are severed
during fracture.
For thermoplastic polymers, both ductile and brittle modes are possible, and
many of these materials are capable of experiencing a ductile-to-brittle
transition. Factors that favor brittle fracture are a reduction in temperature, an
increase in strain rate, the presence of a sharp notch, increased specimen
thickness, and any modification of the polymer structure that raises the glass
transition temperature. Glassy thermoplastics are brittle below their glass
transition temperatures.
One phenomenon that frequently precedes fracture in some thermoplastic
polymers is crazing. Associated with crazes are regions of very localized
plastic deformation, which lead to the formation of small and interconnected
microvoids (Figure 6.a).
Figure 6. Schematic drawings of (a) a craze showing microvoids and

fibrillar bridges, and (b) a craze followed by a crack.
Polymer Types :
9
There are many different polymeric materials that are familiar to us and find
a wide variety of applications; in fact, one way of classifying them is according
to their end use.
Within this scheme the various polymer types include plastics, elastomers
(or rubbers), fibers, coatings, adhesives, foams, and films. Depending on its
properties, a particular polymer may be used in two or more of these
application categories.
For example, a plastic, if cross linked and utilized above its glass transition
temperature, may make a satisfactory elastomer. Or a fiber material may be
used as a plastic if it is not drawn into filaments. This portion of the chapter
includes a brief discussion of each of these types of polymer.
1. Plastics:
Possibly the largest number of different polymeric materials come under the
plastic classification. Plastics are materials that have some structural rigidity
under load, and are used in general-purpose applications. Polyethylene,
polypropylene, poly(vinyl chloride), polystyrene, and the fluorocarbons,
epoxies, phenolics, and polyesters may all be classified as plastics. They have a
wide variety of combinations of properties.
Some plastics are very rigid and brittle (Figure 15.1, curve A). Others are
flexible, exhibiting both elastic and plastic deformations when stressed, and
sometimes experiencing considerable deformation before fracture (Figure 4,
curve B).
Polymers falling within this classification may have any degree of
crystallinity, and all molecular structures and configurations (linear, branched,
isotactic, etc.) are possible. Plastic materials may be either thermoplastic or
thermosetting; in fact, this is the manner in which they are usually sub
classified. However, to be considered plastics, linear or branched polymers
must be used below their glass transition temperatures (if amorphous) or below
their melting temperatures (if semicrystalline), or
must be cross linked enough to maintain their shape.
Several plastics exhibit especially outstanding properties. For
applications in which optical transparency is critical, polystyrene and poly
(methyl methacrylate) are especially well suited; however, it is imperative that
the material be highly amorphous or, if semicrystalline, have very small
crystallites. The fluorocarbons have a low coefficient of friction and are
extremely resistant to attack by a host of chemicals, even at relatively high
temperatures. They are utilized as coatings on nonstick cookware, in bearings
and bushings, and for high-temperature electronic components.
10
The advantages of plastics:-

The grate increase in the use of plastics is due to
- their many useful properties,
- couples with comparatively low cost,
- their low densities,
- their high resistance to chemical attack,
- their thermal and electrical insulation properties,
- their ease of fabrication in to a wide variety of both simple and complex
shapes.
The disadvantages of plastics :-
The main disadvantages of plastics are :
- The low strength and elastic modulus values, in compression with those
of metals
- The low softening and thermal degradation temperature
- Their comparatively high thermal expansion coefficients.
2. Fibers:
The fiber polymers are capable of being drawn into long filaments having at
least a 100:1 length-to-diameter ratio. Most commercial fiber polymers are
utilized in the textile industry, being woven or knit into cloth or fabric.
To be useful as a textile material, a fiber polymer must have a host of rather
restrictive physical and chemical properties. While in use, fibers may be
subjected to a variety of mechanical deformations stretching, twisting,
shearing, and abrasion. Consequently, they must have a high tensile strength
(over a relatively wide temperature range) and a high modulus of elasticity, as
well as abrasion resistance. These properties are governed by the chemistry of
the polymer chains and also by the fiber drawing process.
The molecular weight of fiber materials should be relatively high or the
molten material will be too weak and will break during the drawing process.
Also, because the tensile strength increases with degree of crystallinity, the
structure and configuration of the chains should allow the production of a
highly crystalline polymer.
That translates into a requirement for linear and unbranched chains that are
symmetrical and have regular repeat units. Polar groups in the polymer
11
also improve the fiber-forming properties by increasing both crystallinity and
the intermolecular forces between the chains.
Convenience in washing and maintaining clothing depends primarily on the
thermal properties of the fiber polymer, that is, its melting and glass transition
temperatures.
Furthermore, fiber polymers must exhibit chemical stability to a rather
extensive variety of environments, including acids, bases, bleaches, dry
cleaning solvents, and sunlight. In addition, they must be relatively
nonflammable and amenable to drying.
12
Corrosion & Its Prevention

Introduction :
Corrosion is the slow but continuous eating away of metallic components
by chemical or electrochemical attack. That this is costly and destructive will
be vouched for by any motorist.
Three factors govern corrosion.
• The metal from which the component is made.
• The protective treatment the component surface receives.
• The environment in which the component is kept.
All metals corrode to a greater or lesser degree; even precious metals like
gold and silver tarnish in time, and this is a form of corrosion. Prevention
processes are unable to prevent the inevitable failure of the component by
corrosion; they only slow down the process to a point where the component
will have worn out or been discarded for other reasons before failing due to
corrosion. Let's now look at the three ways in which metals corrode.
• Dry corrosion This is the direct oxidation of metals which occurs when a
freshly cut surface reacts with the oxygen of the atmosphere. Most of the
corrosion-resistant metals such as lead, zinc and aluminum form a dry oxide
film which protects the metal from further atmospheric attack.
• Wet corrosion This occurs in two ways:
a) The oxidation of metals in the presence of air and moisture, as in the
rusting of ferrous metals.
b) The corrosion of metals by reaction with the dilute acids in rain due to
the burning of fossil fuels (acid rain) - for example, the formation of the
carbonate 'patina' on copper. This is the characteristic green film seen on
the copper clad roofs of some public buildings.
• Galvanic corrosion This occurs when two dissimilar metals, such as iron
and tin or iron and zinc, are in intimate contact. They form a simple
1
electrical cell in which rain, polluted with dilute atmospheric acids, acts as
an electrolyte as generated and circulates within the system. Corrosion
occurs with (depending upon its position in the electrochemical series)
being eaten away.
Other metals, in addition to iron and steel, corrode when exposed to the
atmosphere. The green corrosion -product which covers a copper roof, or the
white, powdery film formed on some unprotected aluminum alloys is clear
evidence of this.
Fortunately the reactivity of a metal and the rate at which it corrode is not
related. For example, although aluminum is chemically more reactive than
iron, as soon as it is exposed to the atmosphere it forms an oxide film which
seals the surface and prevents further corrosion from taking place. On the other
hand, iron is less reactive and forms its to oxide film more slowly.
Unfortunately, the iron hydroxide film (rust) is porous and the process
continues unabated until the metal is destroyed.
Types of corrosion:-
1. Atmospheric corrosion
Any metal exposed to normal atmospheric conditions become covered

with an invisible, thin film of moisture. This moisture film is invariably
contaminated with dissolved solids and gases which increase the rate of
corrosion. The most common example of corrosion due to dissolved oxygen
from the atmosphere is the rapid surface formation of 'red rust' on
unprotected ferrous metals. This 'red rust' is a hydroxide of iron and should
not be confused with the blue- black oxide of iron called 'mill-scale' which
is formed by heating iron in dry air.
Once 'rusting' commences the action is self-generating - that is, it will
continue even after the initial supply of moisture and air is removed. This is
why all traces of rust must be removed or neutralized before painting,
otherwise rusting will continue under the paint, causing it to blister and
flake off.
2
2. Galvanic corrosion
It has already been stated that when two dissimilar metals come into
intimate association in the presence of an electrolyte that a simple
electrical cell is formed resulting in the eating away of one or other of the
metals. Metals can be arranged in a special order called the
electrochemical series. This series is listed in Table 1 and it should be
noted that, in this context, hydrogen gas behaves like a metal.
Table 1. Electrochemical series

Metal Electrode
Sodium -2.71 Corroded (anodic)
Magnesium -2.40
Aluminium -1.70
Zinc -0.76
Chromium -0.56
Iron -0.44
Cadmium -0.40
Nickel -0.23
Tin -0.14
Lead -0.12
Hydrogen (reference potential) 0.00
Copper +0.35
Silver +0.80
Platinum + 1.20
Gold + 1.50 Protected ( cathodic)
If any two metals come into contact in the presence of a dilute acid, the
more negative metal will corrode more rapidly and will be eaten away.
3. Corrosion accelerated by mechanical stresses
We have seen that failure of a component may take place due to

corrosion arising from electrolytic action between two different phases in a
microstructure, or between two different materials in a fabricated structure.
Failure of a component may also occur as a result of the complementary
effects of chemical corrosion and mechanical stress. The methods of stress
application may vary and this will affect the extent of corrosion which
occurs. Forms of corrosion in which stress plays a part can be classified as
follows:
3
3.1 Stress Corrosion. In a cold-worked metal the pile-up of dislocations at

crystal boundaries and other points increases the energy in those regions
so that they become anodic to the rest of the structure. Consequently,
corrosion takes place in these regions of high energy and the locked-up
stresses give rise to the formation of cracks which grow progressively
with the continuance of corrosion. A similar process may take place in
components in which unequal heating or cooling has given rise to the
presence of locked-up stresses, as, for example, near to welded joints.
3.2 Corrosion Fatigue. As might be expected, any component which is

subjected to alternating stresses and is working in conditions which
promote corrosion may fail at a stress well below the normal fatigue
limit (3.72). The action of the corrosive medium will tend to be
concentrated at any surface flaw and behave as a focal point for the
initiation of a fatigue crack. Once a crack has been formed it will spread
more rapidly as a result of the corrosive action combined with
alternating stress.
3.3 Fretting Corrosion is allied to corrosion fatigue and occurs particularly

where closely fitting machine parts are subjected to vibrational stresses.
In steel this form of corrosion appears as patches of finely divided ferric
oxide (Fe203).
3.4 Impingement Corrosion refers to the combined effects of mechanical

abrasion and chemical corrosion on a metallic surface. Mechanical
wear can be caused by the impingement of entrained air bubbles or
abrasive particles suspended in the liquid. The impingement of such
media may lead to the perforation of any protective film existing on the
surface. This film may be an oxide, which is cathodic to the exposed
metal beneath. This type of corrosion is encountered in pump
mechanism turbine and tuber carrying sea-water.
4
Factors affecting corrosions:-

1. Structural design
The following factors should be observed during the design stage of a
component or assembly to reduce corrosion to a minimum.
• The design should avoid crevices and corners where moisture may become
trapped, and adequate ventilation and drainage should be provided.
• The design should allow for easy washing down and cleaning.
• Joints which are not continuously welded should be sealed, for
example, by the use of mastic compounds or impregnated tapes.
• Where dissimilar metals have to be joined, high-strength epoxy adhesives
should be considered since they insulate the metals from each other and
prevent galvanic corrosion.
• Materials which are inherently corrosion resistant should be chosen or, if
this is not possible, an anti-corrosive treatment should be specified.
2. Environment
The environment in which the component or assembly is to spend its
service life must be carefully studied so that the materials chosen, or the anti-
corrosion treatment specified, will provide an adequate service life at a
reasonable cost. It would be unnecessary and uneconomical to provide a
piece of office equipment which will be used indoors whit a protective finish
suitable for heavy-duty contractors plant which is going to work on
construction sites in all kinds of weather conditions.
3. Applied or internal stresses

Chemical and electrochemical corrosion is intensified when a metal is
under stress. This applies equally to externally applied and internal stresses,
although more common in the latter case. Internal stresses are usually caused
by cold working and, if not removed by stress-relief heat treatment, results in
corrosive attack along the crystal boundaries. This weakens the metal
considerably more than simple surface corrosion. An example of
intercrystalline corrosion is the 'season cracking' of a brass after severe cold
working.
Intercrystalline corrosion occurs at the grain boundaries of crystals not
only when impurities are present but also when stress concentrations are
present. Grain boundaries are regions of high energy levels, even in very pure
5
metals, so corrosion tends to occur more quickly at the grain boundaries.

Severely cold- worked α brasses are prone to ‘season cracking'. Here,
intercrystalline corrosion follows the grain boundaries until the component is
no longer able to sustain the internal stresses due to cold working. The
component then cracks. This can be prevented by a low-temperature stress
relief annealing process. This low temperature does not cause
recrystallisation but is sufficient to remove the locked up stresses by allowing
the atoms to move small distances nearer to their equilibrium positions.
4. Composition and structure

The presence of impurities in non-ferrous metals reduces their corrosion
resistance. Hence the high level of corrosion resistance exhibited by high-purity
copper, aluminum and zinc. The importance of grain structure has also been
mentioned above, and a fine-grain structure is generally less susceptible to
corrosion than a coarse-grain structure. The inclusion of certain alloying
elements such as nickel and chromium can also improve corrosion resistance -
for example, the stainless steels and cupro-nickel alloys.
5. Temperature
For all chemical reactions there is a critical temperature below which they
will not take place. Since corrosion is the result of chemical or
electrochemical reactions, corrosion is retarded or stopped altogether at low
temperatures. On the other hand, corrosion is at its worst in the hot. humid
atmosphere of the tropical rain forests, and equipment for use in such
environments has to be 'tropicalised' if it is to have a reasonable service life.
High temperatures alone do not increase the rate of corrosion, and corrosion
is virtually nonexistent in arid desert areas of the world. Failure of
mechanical devices in desert environments is due generally to the abrasive
effect of the all-pervasive sand.
6
Metals which resist corrosion
It has already been made clear that metals combine with atmospheric
oxygen and or atmospheric pollutants to a greater or lesser extent. The
following metals, which resist corrosion, react to form impervious,
homogeneous coatings on their surfaces which prevent further corrosion from
taking place, providing these coatings remain undisturbed.
Such as copper, zinc, aluminum , lead, stainless steel, nickel and chromium.
The protection of corrosion:-

There are two principal methods by which corrosion may be prevented or
minimized. First, the metallic surface can be insulated from the corrosive
medium by some form of protective coating. Such coatings include various
types of paints and varnishes, metallic films having good corrosion-resistance
and artificially thickened oxide films. All of these are generally effective in
protecting surfaces from atmospheric corrosion, though zinc coatings are used
to protect iron from the rusting action of water, whilst tin coatings offer
protection against most animal and vegetable juices encountered in the canning
industry.
In circumstances where corrosive action is severe, or where mechanical
abrasion is likely to damage a surface coating, it may be necessary to use a
metal or alloy which has an inherent resistance to corrosion. Such corrosion
-resistant alloys are relatively expensive, so that their use is limited generally
to chemical- engineering plant, marine-engineering equipment and other
special applications.
There are many types of the protection from corrosion, which they are:-
1) The Use of a Metal or Alloy Which Is Inherently Corrosion-resistant
The corrosion-resistance of a pure metal or a homogeneous solid solution is
generally superior to that of an alloy in which two or
more phases are present in the microstructure. As mentioned above,
the existence of two phases leads to electrolytic action when the surface
of the alloy comes into contact with an electrolyte.
Most of the alloys which are used because of their high

corrosion-resistance exhibit solid-solution structures. Aluminum-
7
magnesium alloys containing up to 7-0% magnesium fulfil these conditions

and are particularly resistant to marine atmospheres. Stain less steel of the "18-
8" type is completely austenitic in structure when correctly heat-treated, but
faulty heat-treatment may lead to the
precipitation of carbides and, hence, to corrosion. Although such corrosion is
partly due to the impoverishment of the austenitic matrix in chromium (since it
is mainly chromium carbide which is precipitated), this corrosion is accelerated
by electrolytic action between the carbide particles and the matrix. “Weld-
decay” in steels of this type occurs for similar reasons.
2) Protection by Metallic Coatings

Protection afforded by metallic coatings can be either "direct" or
"sacrificial". Direct protection depends on an unbroken film of metal covering
the article, and if the film becomes broken, corrosion may be accelerated by
electrolytic action between the film and the metal beneath. In the case of
sacrificial protection, however, the metallic film becomes the anode in the
event of a break in the film, and thus dissolves in preference to the surface
beneath. It follows that, when protection is limited to the direct type, as in the
case of tin coatings on steel, the quality of the coating is most important, since
acceleration, and not inhibition, of corrosion would follow a break in the film.
In both cases, of course, protection of the direct type is the fundamental aim of
the metal-coating process, and it is only in the possibility of the coating
becoming broken that the effects of electrolytic action must be considered.
A number of methods are available for the production of metallic coatings.
The most widely used are either electro-plating or dipping the articles to be
coated into a bath of the molten metal. In some cases a successful coating can
be produced by heating the articles to be coated in the finely powdered metal,
whilst specialised use is made of the process known as "cladding".
8
2.1 Cladding.
This process is applicable chiefly to the manufacture of "clad" sheet. The
basis metal is sandwiched between pieces of the coating metal, and the
sandwich is rolled to the required thickness. "Alclad", which is duralumin
coated with pure aluminum, is possibly the best known of these products,
whilst "Niclad" (nickel-coated steel) is also manufactured.
Figure 1. Sectional through clad metal composite.
2.2 Hot-dip Metal Coating

Tin and zinc are the metals most often used to produce metallic coatings in
this manner, though increasing use is being made of aluminum.
(a) Hot-dip Tinning.

(b) Hot-dip Galvanising
(c) Hot-dip Coating with Aluminum.
2.3 Coating by means of a spray of molten metal

Metal spraying consists in projecting "atomised" particles of molten metal
from a special pistol by a stream of compressed air on to a suitably prepared
surface. Surface preparation usually involves blasting the surface with an
abrasive; steel grit having replaced sharp silica sand for this purpose on
account of the silicosis hazards involved when the latter is used. The metal
most commonly used for spraying is zinc, though coatings of aluminium, tin,
lead, solder, cadmium, silver, copper and stainless steel can be deposited in
this way.
In yet another process invented by Dr. Schoop , the originator of metal-

spraying processes, electricity is used in place of gas for heating in those
pistols which utilise zinc wire. In this pistol an arc is struck between two zinc
wires so that their ends melt continuously as the wires are fed forward. The
metal particles are carried forward by a stream of compressed air.
9
Metal spraying has wide application in view of its portability and

flexibility; thus, large structures, such as storage tanks, pylons and bridges,
can be sprayed on site. Notable recent examples include the Forth Road
Bridge and the Volta River Bridge (Ghana), both of which were zinc coated
using modern developments of the Schoop process.
2.4 Electro-plating
The formation of metal coatings by electro-deposition is well known, and a
wide variety of metals can be thus used, including copper, nickel, chromium,
cadmium, gold and silver. Tin and zinc can also be electro-deposited, and a
coating thus formed has advantages over one produced by hot-dipping in
respect of flexibility, uniformity and control of thickness of film.
In the actual process of electro-plating the article to be plated is made the
cathode in an electrolytic cell. Sometimes the metal to be deposited is
contained, as a soluble salt, in the electrolyte, in which case the anode is a non-
reactive conductor, such as stainless steel, lead or carbon. In most cases,
however, the anode consists of a plate of the pure metal which is being
deposited, whilst the electrolyte will contain a salt or salts of the same metal.
Then, the anode gradually dissolves and maintains the concentration of the
metal in the electrolyte as it is deposited on to the articles forming the cathode.
The conditions under which deposition takes place are very important, so
that the cell voltage, the current density (measured in amperes per square meter
of cathode surface), the ratio of anode area to cathode area and the time of
deposition, as well as the composition and temperature of the electrolyte, must
all be strictly controlled if a uniform adherent and non-ferrous film is to be
obtained.
Figure 2. The electro plating.
10
3) Protection by oxide coating
In some instances the film of oxide which forms on the surface
of a metal is very dense and closely adherent. It will then protect the metal
surface beneath from oxidation. Stainless steels owe their resistance to
corrosion to the presence of a high proportion of chromium, which is one of
these elements that form oxide films impervious to oxygen. The "blueing" of
ordinary carbon steel by heating it in air produces an oxide film of such a
nature that it affords partial protection from corrosion.
Anodizing. Reference has already been made to the protection afforded

aluminum by the natural film of oxide which forms on its surface. Anodic
oxidation, or anodising, is an electrolytic process for thickening this oxide film.
This process may be applied for several reasons, such as to provide a "key" for
painting, to provide an insulating coating for an electrical conductor or to
provide a surface which may be dyed, as well as to increase the resistance of
aluminum to corrosion.
Before being anodised the surface of the article must be chemically clean.
Preliminary treatment involves sand-blasting, scratch brushing or barrel
polishing, according to the nature of the component. This is followed by
degreasing in either the liquid or vapour of electrolytic cleaning.
In the actual anodising operation which follows, the aluminum article to be
treated is made the anode in an electrolyte containing either chromic, sulphuric
or oxalic acid; the cathode being a plate of lead or stainless steel. When an
electric current is passed, oxygen is formed at the anode and immediately
combines with the aluminum surface of the article. The layer of oxide thus
formed grows outwards from the surface of the aluminum. The normal
thickness of a satisfactory anodic film produced commercially varies between
0-007 and 0-015 mm., and a film having a thickness within these limits would
be formed by anodising a component in a 15% sulphuric acid solution at 20° C
2
for about thirty minutes, using a current density of about 100 A/m at a cell
voltage of 15. A longer period of treatment produces a thicker, but soft and
spongy, film which would be unsatisfactory in service. The thickness of the
natural film produced on an aluminum surface by exposure to air at normal
temperatures is of the order of 0.000 013 mm.
11
Anodising
Aluminum and aluminum alloy components are cleaned and degreased.
After which they are etched, wire-brushed or polished depending upon the
surface texture required. The work is then made the anode of an electrolytic
cell (see electroplating, where the work is the cathode) and a direct current is
passed through the cell. The electrolyte is a dilute acid and varies with the
finish and protection required. Colours may be integral or applied subsequently
by dyeing. The purpose of the treatment is to increase the thickness of the
natural, protective oxide film and improve the corrosion resistance of the
metal.
4) Protection by other nonmetallic coatings

Coatings of this type usually offer only a limited protection against
corrosion and are, more often than not, used only as a base for painting.
4.1 Phosphating
A number of commercial processes fall under this heading, but in all of
them a coating of phosphate is produced on the surface of steel or zinc-base
alloys by treating them in or with a solution of acid phosphates. In order
that the metal shall be made rust-proof a finishing treatment with varnish,
paint, oil or lacquer is required.
4.2 Chromating
Chromate coatings are produced on magnesium-base alloys, and on zinc
and its alloys, by immersing the articlesin a bath containing potassium
bichromate along with various other additions. The colour of the films
varies with the bath and alloy, from yellow to grey and black.
12
5) Cathodic protection
This method of protection against corrosion can be used for buried or
submerged pipe-lines and other structures. The pipe -line is made to act as a
cathode by burying near it pieces of a metal which is much more
electropositive than the iron of the pipe-line. These pieces of metal will
therefore be anodic towards the iron of the pipe-line and will corrode
sacrificially.
Alternatively, a current from D.C. mains can be passed through the soil or
water on to the metallic surface concerned so as to keep it at a slightly negative
potential with respect to its surroundings. When electric power is available this
will be the cheaper method, since electricity can be obtained more cheaply
from the mains than from any electro-chemical source. To protect the whole
surface of a pipe-line by this means, however, would be expensive, but if the
pipe has already been coated with paint or some other non-metallic substance,
so that it is only necessary to protect any defective areas, the power cost is
small, since very small currents only are necessary. In some parts of America
the current is generated by dynamos driven by windmills.
13
Ceramics
Introduction:
Ceramics are compounds between metallic and nonmetallic elements; they
are most frequently oxides, nitrides, and carbides. For example, some of the
common ceramic materials include aluminum oxide (or alumina,Al 2O3),
silicon dioxide (or silica, SiO2), silicon carbide (SiC), silicon nitride (Si 3N4),
and, in addition, what some refer to as the traditional ceramics those
composed of clay minerals (i.e., porcelain), as well as cement, and glass.
Up until the past 60 or so years, the most important materials in this class
were termed the “traditional ceramics,” those for which the primary raw
material is clay; products considered to be traditional ceramics are china,
porcelain, bricks, tiles, and, in addition, glasses and high-temperature ceramics.
Of late, significant progress has been made in understanding the fundamental
character of these materials and of the phenomena that occur in them that are
responsible for their unique properties.
Consequently, a new generation of these materials has evolved, and the
term “ceramic” has taken on a much broader meaning. To one degree or
another, these new materials have a rather dramatic effect on our lives;
electronic, computer, communication, aerospace, and a host of other industries
rely on their use.
With regard to mechanical behavior, ceramic materials are relatively stiff
and strong stiffnesses and strengths are comparable to those of the metals. In
addition, ceramics are typically very hard. On the other hand, they are
extremely brittle (lack ductility), and are highly susceptible to fracture .
These materials are typically insulative to the passage of heat and electricity
, and are more resistant to high temperatures and harsh environments than
metals and polymers. Several common ceramic objects are shown in the
photograph of Figure 1.
1
Figure 1. Common objects that are made of ceramic materials: scissors, a china tea cup, a
building brick, a floor tile, and a glass vase.
Impurity atoms can form solid solutions in ceramic materials much as they
do in metals. Solid solutions of both substitutional and interstitial types are
possible.
Ceramic Phase Diagrams:

Phase diagrams have been experimentally determined for a large number of
ceramic systems. For binary or two-component phase diagrams, it is frequently
the case that the two components are compounds that share a common element,
often oxygen. These diagrams may have configurations similar to metal–metal
systems, and they are interpreted in the same way.
As an example, one of the relatively simple ceramic phase diagrams is that
found for the aluminum oxide–chromium oxide system, Figure 2.This diagram
has the same form as the isomorphous copper–nickel phase diagram, consisting
of single liquid and single solid phase regions separated by a two-phase solid–
liquid region having the shape of a blade. The solid solution is a substitutional
one in which substitutes for and vice versa. It exists for all compositions below
the melting point of inasmuch as both aluminum and chromium ions have the
same charge as well as similar radii (0.053 and 0.062 nm, respectively).
Furthermore, both Al2O3 and Cr2O3 have the same crystal structure.
2
Figure 2. The aluminum oxide – chromium oxide phase diagram.
Mechanical Properties :
Ceramic materials are somewhat limited in applicability by their
mechanical properties, which in many respects are inferior to those of metals.
Brittle Fracture of Ceramics:

The brittle fracture process consists of the formation and propagation of
cracks through the cross section of material in a direction perpendicular to
the applied load. Crack growth in crystalline ceramics may be either
transgranular (i.e., through the grains) or intergranular (i.e., along grain
boundaries); for transgranular fracture, cracks propagate along specific
crystallographic (or cleavage) planes, planes of high atomic density.
Stress–Strain Behavior:
At room temperature, virtually all ceramics are brittle. Microcracks, the
presence of which is very difficult to control, result in amplification of
applied tensile stresses and account for relatively low fracture strengths
(flexural strengths). This amplification does not occur with compressive
loads, and, consequently, ceramics are stronger in compression.
3
The stress at fracture using this flexure test is known as the flexural
strength, modulus of rupture, fracture strength, or the bend strength, an
important mechanical parameter for brittle ceramics.
Hardness
One beneficial mechanical property of ceramics is their hardness, which
is often utilized when an abrasive or grinding action is required; in fact, the
hardest known materials are ceramics.
Creep
Often ceramic materials experience creep deformation as a result of
exposure to stresses (usually compressive) at elevated temperatures. In
general, the time deformation creep behavior of ceramics is similar to that
of metals; however, creep occurs at higher temperatures in ceramics. High-
temperature compressive creep tests are conducted on ceramic materials to
ascertain creep deformation as a function of temperature and stress level.
Types and Applications of Ceramics:

Most ceramic materials fall into an application-classification scheme that
includes the following groups: glasses, structural clay products, white wares,
refractories, abrasives, cements, and the newly developed advanced ceramics
as shown in Figure 3.
Figure 3. Classification of ceramic materials on the basis of application.
4
1) Glasses
The glasses are a familiar group of ceramics; containers, lenses, and
fiberglass represent typical applications. Most inorganic glasses can be
made to transform from a noncrystalline state to one hat is crystalline by the
proper high-temperature heat treatment. This process is called
crystallization, and the product is a fine-grained polycrystalline material
which is often called a glass–ceramic. The formation of these small glass-
ceramic rains is, in a sense, a phase transformation, which involves
nucleation and growth stages.
Glass-ceramic materials have been designed to have the following
characteristics:
relatively high mechanical strengths;
low coefficients of thermal expansion (to avoid thermal shock);
relatively high temperature capabilities; good dielectric properties (for
electronic packaging applications); and
good biological compatibility.
The most common uses for these materials are as ovenware, tableware,
oven windows, and rangetops—primarily because of their strength and
excellent resistance to thermal shock. They also serve as electrical
insulators and as substrates for printed circuit boards, and are used for
architectural cladding, and for heat exchangers and regenerators.
2) Clay Products
One of the most widely used ceramic raw materials is clay. This
inexpensive ingredient, found naturally in great abundance, often is used as
mined without any upgrading of quality. Another reason for its popularity
lies in the ease with which clay products may be formed; when mixed in the
proper proportions, clay and water form a plastic mass that is very
amenable to shaping. The formed piece is dried to remove some of the
moisture, after which it is fired at an elevated temperature to improve its
mechanical strength.
3) Refractories
Another important class of ceramics that are utilized in large tonnages is
the refractory ceramics. The salient properties of these materials include
the capacity to withstand high temperatures without melting or
decomposing, and the capacity to remain unreactive and inert when
exposed to severe environments. In addition, the ability to provide thermal
insulation is often an important consideration.
5
Refractory materials are marketed in a variety of forms, but bricks are

the most common. Typical applications include furnace linings for metal
refining, glass manufacturing, metallurgical heat treatment, and power
generation.
Of course, the performance of a refractory ceramic, to a large degree,
depends on its composition. On this basis, there are several classifications
namely, fireclay, silica, basic, and special refractories.
4) Abrasives
Abrasive ceramics are used to wear, grind, or cut away other material,
which necessarily is softer. Therefore, the prime requisite for this group of
materials is hardness or wear resistance; in addition, a high degree of
toughness is essential to ensure that the abrasive particles do not easily
fracture. Furthermore, high temperatures may be produced from abrasive
frictional forces, so some refractoriness is also desirable.
Diamonds, both natural and synthetic, are utilized as abrasives; however,
they are relatively expensive. The more common ceramic abrasives include
silicon carbide, tungsten carbide (WC), aluminum oxide (or corundum),
and silica sand.
5) Cements
Several familiar ceramic materials are classified as inorganic cements:
cement, plaster of paris, and lime, which, as a group, are produced in
extremely large quantities.
The characteristic feature of these materials is that when mixed with
water, they form a paste that subsequently sets and hardens. This trait is
especially useful in that solid and rigid structures having just about any
shape may be expeditiously formed. Also, some of these materials act as a
bonding phase that chemically binds particulate aggregates into a single
cohesive structure. Under these circumstances, the role of the cement is
similar to that of the glassy bonding phase that forms when clay products
and some refractory bricks are fired. One important difference, however, is
that the cementitious bond develops at room temperature.
6) Advanced Ceramics
Many of our modern technologies utilize and will continue to utilize
advanced ceramics because of their unique mechanical, chemical, electrical,
magnetic, and optical properties and property combinations.
6
Deformation in Metals
Introduction:
After studying the mechanical properties of metals, we learned that
deformation can occur either by elastic movement or by plastic flow.
Elastic flow in matels:
In elastic deformation a limited distortion of the crystal lattice is produced, but
the atoms do not move permanently from their ordered positions, and as soon
as the stress is removed the distortion disappeared. When metal is stressed
beyond the elastic limit plastic deformation takes place and there must, clearly
, be some movement of the atoms in to new positions, since considerable
permanent distortion can be produced. Our present task, then, is to consider
ways in which this extensive rearrangement of atoms with in the lattice
structure can take place to give rise to this permanent deformation.
Plastic flow in metals:

As mentioned previously, many materials possess an elastic limit and when stressed they
strain in an elastic manner up to a certain point. Beyond THIS developed is no longer directly
proportional to the applied
POINT THE STRAIN
stress, and also, the strain developed is no longer fully recoverable. If the stress
is removed elastic strain is recovered but the material will be left in a state of
permanent, or plastic, strain. The mechanism of plastic deformation is not the
same for all classes of materials and it is necessary to consider the various
materials groups separately. Metals, in general, are characterized by possessing
high elastic modulus values, and also the ability to be strained m a plastic
manner. Some metals will begin to deform plastically at very low values of
stress and will yield to a very considerable extent before fracture occurs. Other
metals and alloys show little plastic yielding before fracture. These latter
materials are termed brittle. Plastic deformation in metals may take place by
the process of slip, or by twinning.
1
1) Slip
It is the deformation done by one layer or plan of atoms gliding over
another.
An early theory evolved to explain plastic deformation in metals was
the 'block slip' theory. In this it was postulated that when the yield stress
of the metal was exceeded plastic deformation took place by the
movement of large blocks of atoms sliding relative to one another across
certain planes — slip planes — within the crystal as shown in Figure 1.
The 'block slip' theory accounted for many of the observed

phenomena but possessed a number of drawbacks, one of which being
that the theoretical yield strength of a metal, calculated on the basis of
this theory, was about a thousand times greater than the experimentally
observed strengths of pure metals. Present-day theories of plastic flow in
metals are based on the existence of small imperfections, or defects,
within crystals. These are structural defects, termed dislocations. and
plastic deformation is due to the movement of dislocations across the
slip planes of a crystal under the action of an applied stress. The
calculated stress required to bring about the movement of dislocations is
of the same order of magnitude as observed yield stresses in metals. In
recent years it has been possible to produce small single crystals that are
virtually defect free. These small perfect crystals, termed whiskers,
possess properties close to the very high theoretical strengths predicted
for perfectly crystalline metals.
2
Figure1.Plastic deformation according to the 'block slip' theory, (a) Original

unstressed condition, (b) Elastic strain only. Specimen will revert to (a) when
the stress is removed, (c) Elastic and plastic deformation. When stress is
removed the specimen will appear as in (d). (d) Unstressed. No elastic strain
but permanent plastic strain remains.
If the slip planes were aligned either normal to, or parallel to, the
stress axis, failure occurred in a brittle manner with negligible plastic
deformation as in Figure 2. If, however, the slip planes were inclined at
some angle, θ, other than 0° or 90°, plastic yielding took place before
failure.
Figure 2. Effect of stress on single crystals of hexagonal metal. (a) Slip planes
normal to the applied stress; brittle fracture; no slip. (b) Slip planes in line
with the applied stress; brittle fracture; no slip. (c) Slip planes inclined to
the applied stress; slip and plastic deformation caused by shear force
acting on slip planes.
3
2) Twinning
In addition to deformation by slip, some metals, notably zinc,
tin and iron, deform by a process known as "twinning". The mechanism of
this process is illustrated in Figure 3. In deformation by slip all atoms in one
block move the same distance, but in deformation by twinning, atoms in
each successive plane within a block will move different distances, with the
effect of altering the direction of the lattice so that each half of the crystal
becomes a mirror image of the other half. It is thought that twinning also
proceeds by the movement of dislocations. The twins thus formed are called
"mechanical twins" to distinguish them from the "annealing twins" which
become apparent in copper alloys during an annealing operation which
follows cold work. The mechanical twins formed in iron by a sudden shock
are called "Neumann bands".
Figure 3. The formation of "Mechanical Twins".
4
Plastic deformation and strain hardening:

When a metal is stressed beyond its elastic limit dislocations within the
metal begin to move and plastic deformation occurs. The movement of one
dislocation through a lattice will give one increment of plastic deformation,
namely a displacement of the order of one atomic spacing. The movement of
extremely large numbers of dislocations would be necessary to give a visible
amount of plastic slip and the number of dislocations that would need to be
present to account for the large amount of plastic deformation that takes place
in commercial metal- working processes such as rolling or forging would be so
great as to mean that there would be virtually no regular sections of lattice at
all. In fact, the number of dislocations present in a fully annealed metal is
comparatively small and additional dislocations are generated during plastic
deformation.
Energy of Mechanical Deformation:

As deformation proceeds, the metal becomes harder and stronger, and,
whether by slip or by twinning, a stage is reached when no more deformation
can be produced. An increase in the applied force will then lead only to
fracture. In this state, when tensile strength and hardness have reached a
maximum and elongation a minimum, the material is said to be work-
hardened. Thus we can summarise the effects of mechanical deformation
briefly as follows - if sufficient stress is applied to a metal, slip (or twinning)
will take place in individual crystals. As deformation proceeds, the capacity for
slip decreases that the force necessary to produce it must increase. A point is
reached, coinciding with the maximum resistance to slip (the maximum
strength and hardness), where no more deformation is possible and fracture
will take place. The material must then be annealed if further cold work is to be
carried out on it.
During a cold -working process approximately 90 % of the mechanical

energy employed is turned into heat, whilst the remaining 10 % is stored inside
the material as mechanical potential energy. The bulk of this stored energy (9
% of that originally employed) is that associated with the number of
dislocations present. These have energy because they distort the lattice and
cause atoms to occupy positions of higher-than-minimum energy. The
remaining stored energy (1 % of the energy
5
originally employed) exists as locked-up residual stresses arising from elastic

strains internally balanced.
The increased-energy state of a cold-worked metal makes it chemically more
active and consequently less resistant to corrosion. This is particularly true of
micro-stresses acting at grain boundaries and leading
' increased intercrystalline corrosion by causing the grain boundaries to
corrode more quickly than the rest of the material. This stored potential energy
is also the main driving force of recrystallisation.
Annealing and Recrystallisation:

A cold-worked metal is in a state of considerable mechanical stress,
resulting from elastic strains internally balanced. These elastic strains are
largely due to unhomogeneous deformation having taken place during
cold-working. If the metal is heated to a sufficiently high
'erature these strains will be removed; at the same time the tensile
strength and hardness of the metal will fall to approximately their
original value and the capacity for cold -work return. This form of heat
treatment is known as annealing, and is made use of when the metal is required
for use in a soft but tough state or, alternatively, when it is to undergo further
cold deformation. Annealing takes place in three stages as follows:
Stage I - The Relief of Stress

Stage II - Recrystallisation.
Stage III - Grain Growth.
6
The industrial shaping of metals
Introduction:
Materials have to be processed into a great variety of shapes in order to
make component parts of every type. The shapes required vary enormously,
both in size and complexity, ranging from micro-electronic components to
large castings and forgings of , perhaps, several hundred tones mass (1 tones =
1000 kg = 1 Mg). The engineer must have some awareness of the range of
manufacturing processes available, and of the advantages and limitations of the
various processes. The properties of the material in the finished component are
also influenced to a considerable extent by the type of shaping process
employed, and by the conditions existing during processing.
Metals and alloys may be shaped into something approaching the final
required form by one of the following operations:
(a) casting into either a sand or a metal mould;
(6) casting as an ingot followed by a hot-working process;
(c) casting as an ingot followed by a cold-working process;
(d) sintering from a powdered metal.
There are, it is true, other processes, such as electro-deposition and the
condensation of metal vapours, but these operations are usually confined to the
surface treatment of metallic components rather than to their actual shaping.
Electro- deposition is sometimes used to build up parts which have become
badly worn.
1
FORMING OPERATIONS
Forming operations are those in which the shape of a metal piece is changed
by plastic deformation; for example, forging, rolling, extrusion, and drawing
are common forming techniques. Of course, the deformation must be induced
by an external force or stress, the magnitude of which must exceed the yield
strength of the material. Most metallic materials are especially amenable to
these procedures, being at least moderately ductile and capable of some
permanent deformation without cracking or fracturing.
When deformation is achieved at a temperature above that at which
recrystallization occurs, the process is termed hot working ; otherwise, it is
cold working. With most of the forming techniques, both hot- and cold-
working procedures are possible. For hot-working operations, large
deformations are possible, which may be successively repeated because the
metal remains soft and ductile. Also, deformation energy requirements are less
than for cold working.
However, most metals experience some surface oxidation, which results in
material loss and a poor final surface finish. Cold working produces an
increase in strength with the attendant decrease in ductility, since the metal
strain hardens; advantages over hot working include a higher quality surface
finish, better mechanical properties and a greater variety of them, and closer
dimensional control of the finished piece. On occasion, the total deformation is
accomplished in a series of steps in which the piece is successively cold
worked a small amount and then process annealed ; however, this is an
expensive and inconvenient procedure.
An example of the forming operations are illustrated schematically in Figure
1.
Figure 1. Metal deformation during (a) forging, (b) rolling, (c) extrusion, and (d) drawing.
2
1. Casting
Casting is a fabrication process whereby a totally molten metal is poured
into a mold cavity having the desired shape; upon solidification, the metal
assumes the shape of the mold but experiences some shrinkage. Casting
techniques are employed when (1) the finished shape is so large or complicated
that any other method would be impractical, (2) a particular alloy is so low in
ductility that forming by either hot or cold working would be difficult, and (3)
in comparison to other fabrication processes, casting is the most economical.
Furthermore, the final step in the refining of even ductile metals may involve a
casting process. A number of different casting techniques are commonly
employed, including sand, die, investment, lost foam, and continuous casting.
Only a cursory treatment of each of these is offered.
Sand Casting
With sand casting, probably the most common method, ordinary sand is
used as the mold material. A two- piece mold is formed by packing sand
around a pattern that has the shape of the intended casting. Furthermore, a
gating system is usually incorporated into the mold to expedite the flow of
molten metal into the cavity and to minimize internal casting defects. Sand-
cast parts include automotive cylinder blocks, fire hydrants, and large pipe
fittings.
Figure 2. Mould for a Sand-casting.
Die Casting
In die casting, the liquid metal is forced into a mold under pressure and at a
relatively high velocity, and allowed to solidify with the pressure maintained. A
two piece permanent steel mold or die is employed; when clamped together,
the two pieces form the desired shape. When complete solidification has been
achieved, the die pieces are opened and the cast piece is ejected. Rapid casting
rates are possible, making this an inexpensive method; furthermore, a single
3
set of dies may be used for thousands of castings. However, this technique
lends itself only to relatively small pieces and to alloys of zinc, aluminum, and
magnesium, which have low melting temperatures.
Figure 3. A Pressure Die-casting Machine.
2. Hot Working
Any increase in the temperature of a metal leads to an increase in atomic
spacings so that the bond strength will decrease slightly. Moreover, a
dislocation does not produce as much distortion and can move more easily
through the crystal. Consequently the yield strength falls as the temperature
rises.
However, hot-working operations invariably take place above the
recrystallisation temperature of a metal or alloy. The importance of this will be
at once apparent. Deformation and recrystallisation will be taking place
simultaneously, so that a considerable speeding-up of the process is possible,
with no tedious inter-stage anneals as are necessary in cold-deformation
processes.
Moreover, with most alloys, malleability and plasticity are considerably
increased at high temperatures, so that far less power is needed to produce
deformation. With some alloys it is essential to use a hot-working process,
since they are hard or brittle when cold, owing to the presence of a hard micro-
constituent which is absorbed at the hot- working temperature.
There are many types of hot working processes which are: Hot –rolling,
Forging, Prop-forging, Heading, Hot-pressing and Extrusion. The main
hot-working processes are dealt with are below:
4
- Hot – rolling
Hot-rolling is universally applied to the "breaking-down" of large steel
ingots to sections, strip, sheet and rod of various sizes. In fact, the only
conditions under which cold-work is applied to steel are when the section is
too small to retain its heat, or when a superior finish is required in the
product.
A steel-rolling shop consists of a powerful "two-high" reversing mill, to
break down the white-hot ingots, followed by trains of rolls which will be
either plain or grooved according to the type of product being
manufactured. Hot-rolling is similarly applied to most of the non-ferrous
alloys in the initial breaking-down stages, but the finishing operations are
more likely to involve cold-work.
- Forging
The simplest and most ancient working process known to metallurgical
industry is essentially that which was employed by Tubal Cain, and which
is still employed by a skilled blacksmith. Although power-driven hammers
are now used, skill is still necessary on the part of the smith, since he works
with comparatively simple shaping tools known as "swages".
Wrought iron is always associated with the blacksmith, but many other
ferrous and non-ferrous alloys can be shaped by both hand and mechanical
forging processes. During forging, the coarse "as-cast" structure is broken
down and replaced by one which is of relatively fine grain. At the same
time impurities are redistributed in a more or less fibrous form. Therefore it
is more satisfactory, all other things being equal, to forge a component than
to cast it to shape.
- Extrusion
The extrusion process is now used for shaping a variety of ferrous and non-ferrous metals and alloys.
Its most important feature is that we are able to force the metal through a die, and, in a single
process from the cast billet, to obtain quite complicated sections of

tolerably accurate dimensions. The metal billet is heated to
the required extrusion temperature and placed in the container of the
extrusion press. The ram is then driven hydraulically with sufficient
pressure to force the metal through a hard alloy-steel die.
5
the solid metal section issues from the die in a manner similar to the flow of
toothpaste from its tube.
Using this process, a wide variety of sections can be produced, including
round rod, hexagonal brass rod (for parting off as nuts), brass curtain rail,
small-diameter rod (for drawing still further to wire), tubes 'tress-bearing
sections in aluminum alloys (mainly for aircraft construction).
Figure 4. Extrusion (a) commencement of extrusion stroke; (b) completion

of extrusion stroke.
3. Cold Working
Cold-working from the ingot to the finished product, with, of course, the
necessary intermediate annealing stages, is applied only in the case of a few
alloys. These include both alloys which are very malleable in the cold and, on
the other hand, those which become brittle when heated.
Cold-working is more often applied in the finishing stages of production.
Then its functions are:
(a) to enable accurate dimensions to be attained in the finished product
(b) to obtain a clean, smooth finish;
6
(c) by adjusting the amount of cold-work in the final operation after annealing,
to obtain the required degree of hardness, or "temper", in alloys which
cannot be hardened by heat-treatment.
Raising the temperature of an alloy generally increases its malleability, but
reduces its ductility because of the attendant reduction in yield strength. Thus
in hot-working processes we are always pushing the alloy into shape, whilst in
cold-working operations we frequently make use of the high ductility of some
alloys when cold, by pulling them into their required shapes. Therefore,
processes involving the putting or "drawing" of metal through a die are always
cold-working operations.
There are many cold -working processes, but the principal ones used in
metallurgical industries are below:
Cold-rolling, Drawing of solid and Hollow sections, Cold-pressing and

Deep-drawing, Coining and Spinning.
- Cold-rolling.
Cold- rolling is applied during the finishing stages of production of both
strip and section and also in the production of very thin materials such as foil.
In most other cases cold-rolling mills are similar in design to those used for
hot-rolling. The production of mirror-finished metal foil is carried out in rolls
enclosed in an "air-conditioned" cubicle, and the rolls themselves are polished
frequently with clean cotton wool. Only by working in perfectly clean
surroundings, with highly polished rolls, can really high grade foil be obtained.
In addition to quality of finish, the objects of cold- rolling are accuracy of

dimensions and the adjustment of the correct temper in the material.
- Coining
Coining, or embossing, is really a cold-forging process and, as its name
implies, it is used for the production of coinage, medallions and the like. It has
also been used on an experimental scale for producing engineering components
to exact dimensions. A malleable alloy is essential for this type of process if
excessive wear on the dies is to be avoided.
7
4. Sintering from a Powder

This method of producing metallic structures has become increasingly
important in recent years, and is particularly useful when there is a big
difference in the melting points of the metals to be alloyed, or when a metal
has an extremely high melting point. As an example, products containing a
high proportion of tungsten are usually formed by sintering, since this metal is
difficult and expensive to melt on a commercial scale.
The metal to be sintered is obtained as a fine powder, either by grinding; by

volatilisation and condensation; or by reduction of its powdered oxide. Any
necessary mixing is carried out, and the mixed powdered metals are then
placed in a hardened steel die and compressed. The pressures used vary with
2
the metals to be sintered, but are usually between 70 and 700 N mm . The
brittle compressed mass is then heated in a small electric furnace to a
temperature which will cause sintering to take place and produce a
mechanically satisfactory product. Sintering will often occur below the melting
point of either metal, though frequently it is above the melting point of one of
them.
8
Composite materials
Introduction:
As was mentioned that alloys of metals with non- metals could only occur if
all the component materials were miscible, that is, soluble in each other in the
molten state. Composite materials can be made up from materials that are not
soluble in each other. Composite materials are not alloys.
In its simplest form a composite material consists of two dissimilar
materials in which one material forms a matrix to bond together the other
(reinforcement ) material. The matrix and reinforcement are chosen so that
their mechanical properties complement each other, whilst their deficiencies
are neutralised. For example, in GRP moulding, the polyester resin is the
matrix that binds together the glass fiber reinforcement.
Material property combinations and ranges have been extended by the
development of composite materials. Generally speaking, a composite is
considered to be any multiphase material that exhibits a significant proportion
of the properties of both constituent phases such that a better combination of
properties is realized. According to this principle of combined action, better
property combinations are fashioned by the judicious combination of two or
more distinct materials. Property trade-offs are also made for many composites.
In designing composite materials, scientists and engineers have ingeniously
combined various metals, ceramics, and polymers to produce a new generation
of extraordinary materials. Most composites have been created to improve
combinations of mechanical characteristics such as stiffness, toughness, and
ambient and high-temperature strength.
In a 'composite', the reinforcement material, in the form of rods, strands,
fibers or particles, is bonded together with the other matrix materials. For
example, the fibers may have some of the highest moduli and greatest strengths
available in tension, but little resistance to bending and compressive
1
forces. On the other hand, the matrix can be chosen to have high resistance to
bending and compressive forces. Used together these two different types of
material produce a composite with high tensile and compressive strengths and
a high resistance to bending.
Structural Composites
A structural composite is normally composed of both homogeneous and
composite materials, the properties of which depend not only on the properties
of the constituent materials but also on the geometrical design of the various
structural elements. Laminar composites and sandwich panels are two of the
most common structural composites; only a relatively superficial examination
is offered here for them.
LAMINAR COMPOSITES
A laminar composite is composed of two-dimensional sheets or panels that
have a preferred high-strength direction such as is found in wood and
continuous and aligned fiber-reinforced plastics. The layers are stacked and
subsequently cemented together such that the orientation of the high-strength
direction varies with each successive layer in Figure 1. For example, adjacent
wood sheets in plywood are aligned with the grain direction at right angles to
each other. Laminations may also be constructed using fabric material such as
cotton, paper, or woven glass fibers embedded in a plastic matrix. Thus a
laminar composite has relatively high strength in a number of directions in the
two-dimensional plane; however, the strength in any given direction is, of
course, lower than it would be if all the fibers were oriented in that direction.
Figure 1. The stacking of successive oriented, fiber-reinforced layers for a laminar

composite.
2
Brittle materials such as concrete and ceramics are strong in compression

but weak in tension since they are susceptible to crack propagation, as shown
in Figure 2 (a) . The use of composite materials overcomes this problem by
preventing the crack from 'running'. Two ways in which a crack can be
prevented from running are:
• The use of lamination, as shown in Figure 2(b).
• The use of reinforcing fibres which hold the brittle matrix in compression,
so an external tensile load cannot open up any surface cracks and
discontinuities (Figure 2(c).
Figure 2. Principles of reinforced composite materials: (a) crack propagation in a non-

reinforced ceramic material, (b) behavior of a laminated composite when in tension; ic)
fibre reinforcement
3
PLYWOOD
Wood like all materials reinforced by parallel fibres, has highly directional
strength characteristics. Figure 3(a) shows a plank being bent in a plane
perpendicular to the lay of the grain. Loading the plank in this way exploits its
greatest strength characteristics. Figure 3(b) shows what would happen if a
piece of wood is loaded so that bending occurs parallel to the lay of the grain.
The wood breaks easily since the lignin bone is relatively weak compared with
the natural cellulose reinforcement fibres.
Figure 3. Effect of the direction of grain on the strength of wood.
Plywood overcomes this problem and is a man-made composite which

exploits the directivity of the strength of natural wood. Figure 4, shows how
plywood is built up from veneers (thin sheets of wood) bonded together by a
high-strength and water- resistant synthetic resin adhesive. When laying up the
veneers, care is taken to ensure that the grain of each successive layer is
perpendicular (at right angles) to the preceding layer. When the correct number
of veneers have been laid up, the adhesive component of the composite is
cured under pressure in a hydraulic press.
4
Figure 4. Structure of plywood.
SANDWICH PANELS
Sandwich panels, considered to be a class of structural composites, are
designed to be light-weight beams or panels having relatively high stiff nesses
and strengths. A sandwich panel consists of two outer sheets, or faces, that are
separated by and adhesively bonded to a thicker core as shown in Figure 5. The
outer sheets are made of a relatively stiff and strong material, typically
aluminum alloys, fiber-reinforced plastics, titanium, steel, or plywood; they
impart high stiffness and strength to the structure, and must be thick enough to
withstand tensile and compressive stresses that result from loading. The core
material is lightweight, and normally has a low modulus of elasticity. Core
materials typically fall within three categories: rigid polymeric foams (i.e.,
phenolics, epoxy, polyurethanes), wood (i.e., balsa wood), and honeycombs.
Figure 5. Schematic diagram showing the cross section of a sandwich panel.
5
Structurally, the core serves several functions. First of all, it provides

continuous support for the faces. In addition, it must have sufficient shear
strength to withstand transverse shear stresses, and also be thick enough to
provide high shear stiffness (to resist buckling of the panel). (It should be
noted that tensile and compressive stresses on the core are much lower than on
the faces.)
Another popular core consists of a “honeycomb” structure—thin foils that
have been formed into interlocking hexagonal cells, with axes oriented
perpendicular to the face planes; Figure 6 shows a cutaway view of a
honeycomb core sandwich panel. The honeycomb material is normally either
an aluminum alloy or aramid polymer. Strength and stiffness of honeycomb
structures depend on cell size, cell wall thickness, and the material from which
the honeycomb is made. Sandwich panels are used in a wide variety of
applications including roofs, floors, and walls of buildings; and, in aerospace
and aircraft (i.e., for wings, fuselage, and tailplane skins).
Figure 6. Schematic diagram showing the construction of a honeycomb core sandwich

panel.
Fiber reinforcement
Technologically, the most important composites are those in which the
dispersed phase is in the form of a fiber. Design goals of fiber-reinforced
composites often include high strength and/or stiffness on a weight basis.
These characteristics are expressed in terms of specific strength and specific
modulus parameters, which correspond, respectively, to the ratios of tensile
strength to specific gravity and modulus of elasticity to specific gravity.
This method of reinforcement can range from the glass fibres used in GRP
plastic mouldings to the thick steel rods used to reinforce concrete.
6
1. Reinforced concrete
Concrete itself is a particle-reinforced material. It consists of a mortar
made from a hydraulic cement and sand. reinforced with an aggregate of
chipped stones as shown in figure 7. The stones are crushed so that they
have a rough texture and sharp corners that will key into and bond with
the mortar matrix. This basic concrete has a very high compressive
strength but is very weak in tension. To improve its performance overall,
metal reinforcing rods are added, as shown in Figure 8.
As well as the amount of reinforcement, the positioning of the

reinforcement is also important. Since concrete is strong in compression
but weak in tension, it would seem sensible to insert the reinforcement
near the tension side of the beam, as shown in figure 8. The tension side
is the side of the beam that is on the outside of the 'bend' when the beam
'gives' under the effect of an externally applied load.
Figure 7. Structure of concrete.
Figure 8. Simple reinforced concrete beam.
7
2. Glass- reinforced plastic (GRP)

This important composite material is produced when a plastic material,
usually a polyester resin is reinforced with glass fibre in strand or mat form.
The resin is used to provide shape, colour and finish, whilst the glass fibres,
which are laid in all directions, impart mechanical strength.
When a GRP moulding is correctly 'laid up', the thick, viscous resin
completely surrounds and adheres to the glass fibres of the 'chopped strand
mat' or the woven fibre glass cloth. The resin sets to give a hard. rigid
structure. To shorten the setting time a catalyst (accelerator) is often added to
the resin immediately before moulding. To improve the appearance of the
'rough side' of the moulding (the side not in contact with the polished surface
of the mould), a surfacing tissue is added made up from finer strands of mat.
As shown in Figure 9, Glass-reinforced plastic is widely used for products that
require high strength to weight ratios such as boat hulls, car bodies, gliders,
etc. It has the advantages of being resistant to most environments and it can be
used to form more complex shapes than is possible in wood or sheet metal.
Figure 9. Composition of a GRP lay up.
3. Carbon fibres
These have a higher elastic modulus and lower density than glass fibres,
and can be used to reinforce composite materials having a higher strength to
weight ratio. Carbon fibers are used as a reinforcement in polymeric materials
for a wide range of lightweight, high-strength applications. For example,
carbon fibres are used in the manufactures of gas turbine fan blades, racing car
body panels, high-performance tennis racket frames and high-performance golf
club shafts.
8
Welding
Introduction:
Welding is an operation of joining metals and alloys. Thus differences
between the weld metal and the pieces being joined are structural rather than
compositional.
There are many types of joining materials and the alloys which they are :
1) Soft soldering
2) Brazing
3) Welding
There are two types of welding :
1. Fusion welding processes
2. Solid – phase welding processes
1. Fusion welding
In fusion welding any additional material added to the joint has a similar
composition and strength to the metals being joined. . Figure 1 shows the
principle of fusion welding, where not only the filler metal but also the edges
of the components being joined are melted. The molten metals fuse together
and, when solid, form a homogeneous joint whose strength is equal to the
metals being joined.
1
Figure 1. Fusion welding: (a) before - a single 'V' butt requires extra metal: (b) after - the edges of the
'V' are ,melted and fused together with the molten filler metal.
The fusion welding have some specifications which in this operation the
material that is welded is molten a partionally moltution, no using for pressure
in this operation, the space between the welded materials are filled with a filler.
There are several way to fusion weld such as : oxyacetylene, metallic arc,
atomic hydro, laser welding, we will study the most important ways:
a) Oxyacetylene welding
In this process the heat source is a mixture of oxygen and acetylene burning
:
to produce a flame whose temperature can reach 3250 C. and this is above the
melting point of most metals. Figure 2 shows a typical set of welding
equipment. The welding gases form a highly flammable and even explosive
mixture, so this equipment must only be used by a suitably qualified person or
a trainee under the direct instruction of such a person.
2
Figure 2 Oxyacetylene welding equipment
b) Metallic arc welding

This is a fusion-welding process where the heat energy required to melt the
edges of the components being joined and also the filler rod is supplied by an
electric arc. The arc is the name given to the prolonged spark struck between
two electrodes. In this process the filler rod forms one electrode and the work
forms the other electrode. The filler rod/electrode is coated with a flux which
melts and shields the joint from atmospheric oxygen at the very high
:
temperatures involved. (Average arc temperature is about 6000 C.) The flux
also stabilises the arc and prevents the rod from short circuiting against the
sides of the when welding thick metal. Figure 3 compares the principles of gas
and metallic welding.
3
Figure 3 Comparison of (a) oxyacetylene welding and (b) manual metallic arc welding.
As with gas welding, arc-welding equipment must not be used by untrained

persons except under the closest supervision.
2. Solid-phase welding
In this method the material which are welded dose not fusion, it use an out
pressure to weld so it is not using any external material in the welding process.
There are several ways to weld in the solid-phase welding such as spot
welding , seam welding, cold-pressure welding and friction welding etc…
Effect of welding on the structure and properties of materials:

The structures in a welded joint range from the wrought structures of the parent
metal to the cast structures of the weld itself, all of which will have been subjected
to heat treatment by the high temperatures involved in the process. The weld
deposit will possess a typical cast structure with all its inherent defects. The heat-
affected-one of the parent metal will exhibit the effects of heat treatment. The
unaffected regions, where the temperature has not been so high, will retain
4
the original wrought structure of the parent metal. Therefore the effects of
welding can be studied under the following headings:
• The weld-metal deposit.

• The heat-affected zone.
1. The weld-metal deposit

As previously stated, the weld metal can be considered as a miniature casting
which has cooled rapidly from an extremely high temperature. Long columnar
type crystals may be formed giving rise to a relatively weak structure, as shown in
Figure 4 (a). In a multi-run weld each deposit normalises the preceding run and
considerable grain refinement occurs with a consequent improvement in the
mechanical properties of the joint, as shown in Figure 4 (b).
Figure 4. Weld metal deposit structure: (a) large single-run weld; (b) metallic arc weld.
5
Non-metallic inclusions
The formation of oxide and nitride inclusions due to atmospheric

contamination is reduced by the blanket of burnt gases (products of
combustion) in the case of gas welding, and by the use of a flux when electric
arc welding. Modern flux-coated electrodes usually provide good quality weld
deposits free from harmful inclusions. In the argon arc-welding process the
metal is deposited under a shroud of the inert gas argon. This prevents
oxidation and the formation of nitrides, so no flux is necessary. Further, since
no flux is required there will be no slag inclusions. In multi-run welds using
coated electrodes the slag must be removed between each run.
Gas porosity
The chief cause of gas porosity is the presence of hydrogen in the weld metal or
the formation of steam from the reaction of hydrogen with any oxide present in
the molten parent metal. In addition, hydrogen is present in the welding flame
when gas welding and in the flux coatings of electrodes when arc welding.
Weld-metal cracking
Welded joints that are prepared under restraint are liable to intercrystalline
cracking in the weld deposit due to contractional strains set up during the
cooling of the metal. Such cracking, usually known as 'hot cracking', is largely
related to the grain size and the presence of grain boundary impurities. At high
temperatures, the grain boundaries are more able to accommodate shrinkage
strains than the grains themselves. A coarse grain deposit with large columnar
crystals possesses a relatively small grain boundary area and is, therefore, more
susceptible to hot cracking.
6
2. The heat-affected zone

The heat-affected zone of the parent metal is difficult to define. It will
depend upon such factors as:
• The temperature of the weld pool.

• The time taken to complete the weld.
• The thermal conductivity of the parent metal.
• The specific heat of the parent metal and the dimensions of the
parent metal.
• The method of welding used.
Welded joints produced in metals such as copper and aluminum that have a
high thermal conductivity will have a wider heat-affected zone than a plain
carbon steel that has a lower thermal conductivity. Metallic arc welding
produces a more concentrated heating effect than gas welding. The heat energy
output is greater with arc welding, so the welding process can proceed more
quickly. Therefore the heat-affected zone when arc welding will be narrower
than that when gas welding the same materials.
The heat-affected zone in mild steel plate can exhibit various structures These
range from an overheated structure for those parts adjacent to the weld pool
and, therefore, heated to well above the upper critical temperature, to those
parts whose temperature has hardly risen above room temperature. These are
shown in Figure 5 for both a single-run oxyacetylene weld, and a single-run
metallic arc weld.
7
Figure 5 Macrostructure of single-run welds in mild steel: (a) oxyacetylene weld; (b)
metallic arc weld.
The properties of the material will change with these changes in structure.
The coarser grains will show greater ductility and softness but reduced
strength. The finer crystals will show less ductility but greater hardness and
strength. These effects become more apparent as the carbon content of the steel
increases.
8
Modes of Failure Analysis

Introduction:
- Allowable working stress
Although we describe many methods of testing on the materials, the
materials may also still fail in service, sometimes with disastrous results (e.g.
when the failure occurs in aircraft, bridges, ships, etc.). To try to avoid such
disasters occurring, the designer avoids using materials continuously at their
maximum allowable stress. This is done by employing a factor of safety.
Unfortunately, increasing the strength of a component in the interests of safety
not only increases the initial material costs, but also the operating costs.
-Failure of materials in service
It is essential that engineered products are designed in such a way that any
stresses that are encountered in service are insufficient to cause failure. We
have already looked at the need to introduce a factor of safety where the design
stress does not exceed 50 % of the yield stress.
However, despite such allowances, components still fail in service and
designers now recognize that operating conditions produce brittleness. fatigue,
creep and /or environmental attack which, if ignored, will ultimately lead to
failure. For instance, during the Second World War, cargo ships were being
built quickly and cheaply using welded construction in place of the traditional
riveting. A disturbing number of these ships broke up under storm conditions in
the North Atlantic despite being correctly stressed. It wasn't known at that time
that the cold - near arctic - conditions of the Atlantic winter caused
embrittlement and failure of welded joints in the materials then being used.
1
1. Creep
Creep is a phenomena usually occurs at elevated temperatures since slip in
the lattice structure is easier at such temperatures. Since creep leads to
dimensional change, it becomes an important design factor in steam and gas
turbines. The materials selected for the rotor and stator turbine blades must be
carefully chosen to minimize this effect. It would be catastrophic if the rapidly
rotating blades of the rotor touched the stator blades due to dimensional change
through creep.
So creep can be defined as the gradual extension of a material under a
constant applied load. It is a phenomenon which must be considered in the case
of metals when they are required to work continuously at high temperatures.
For example, the blades of jet engines and gas turbines. Figure
1. shows a typical creep curve for a metal at high temperature. A constant
tensile load is applied to a test piece in a tensile testing machine whilst the test
piece is maintained at a constant elevated temperature.
The creep curve obtained from this test shows three distinct periods of creep.
• Primary creep This commences at a fairly rapid rate but slows down as
work hardening (strain hardening) sets in and the strain rate decreases. It
can be seen from Figure 1. that the extension due to creep is additional to
the instantaneous elongation of material to be expected when any tensile
load is applied. For calculating creep as a percentage elongation, the initial
elongation is ignored and creep is considered to commence at point A on
the curve.
• Secondary creep During this period of creep the increase in strain is
approximately proportional to time. That is the strain rate is constant and at
its lowest value.
• Tertiary creep During this period of creep the strain rate increases rapidly,
necking occurs and the test piece fails. Thus the initial stress, which was
within the elastic range and did not produce early failure, did eventually
result in failure after some period of time.
2
Figure 1. Creep.
Creep, for all materials, is calculated in the same manner as elongation

when associated with a tensile test. That is:
elongation
creep % = ——————— x 100
original length
The difference between the elongation determined from a tensile test and
the creep for the same material is that the former reflects the immediate
response of the material to the applied load, whereas the latter reflects the
response of the material after the load has been applied for a very long period
of time. (This can be several thousand hours).
2. Fatigue
Since more than 75 % of failures in engineering components are attributed
to fatigue failure, and as the performance from engineering products is
continually increased, the need to understand the failure of materials from
fatigue becomes increasingly important.
In service, many engineering components undergo between thousands and
millions of changes of stress within their working life. A material which is
3
subjected to a stress which is alternately applied and removed a very large

number of times, or which varies between two limiting values, will fracture at
a very much lower value of stress than in a normal tensile test. This
phenomenon is referred to as fatigue failure.
It can be seen to be a particular case of brittle fracture were failure occurs
under conditions of repeatedly changing stress. The change can be in
magnitude, direction or both.
The source of these alternating stresses can be due to the service conditions
of the component - for example, the flexing of the valve springs in a car
engine, or the vibration of the axles of a vehicle caused by irregularities in road
surfaces. The fatigue crack which ultimately causes fatigue failure usually
starts at a point of stress concentration such as a sharp corner (incipient crack),
a tooling mark due to machining with too coarse a feed, or a surface crack due
to faulty heat treatment. Also for example the Aircraft wings and rotating shafts
are examples of members subjected to alternating stresses, and where similar
stresses are to be encountered careful consideration at the design stage and
during subsequent maintenance is extremely important if fatigue failure is to be
avoided.
Most fractures which have occurred due to fatigue have a distinctive
appearance, as shown in figure 2. The point of origin of the failure can be seen
as a smooth flat elliptical area. Surrounding this is a burnished zone with
ribbed markings. This is caused by the rubbing together of the surfaces of the
spreading crack due to stress reversals. When the cross-section of the
component will no longer be able to carry its designed load and fail suddenly,
leaving a crystalline area visible as shown in figure 2.
Figure 2. Appearance of fatigue failure.
4
The stages of fatigue failure are shown in figure 3. The fracture always starts
from a point of stress concentration caused by a discontinuity such as:
• Poor surface finish.
• A crack.
• A machining mark.
• An inclusion (foreign particle) in the metal.
Figure 3. The stages of fatigue failure.
Factors affecting fatigue :

- As metals
Many factors affect the fatigue resistance of metals but the most important
are below:
Design, surface finish, temperature, residual stresses and corrosion.
- As polymers
While the factors that affect the fatigue of polymers are:
Temperature, environment and strong sunlight.
5
3. Fracture
Fracture can be classified either as brittle fracture or ductile fracture, and
depends upon the stress at which it occurs in relation to the elastic plastic
properties of the material. This is shown in Figure 4.
Figure 4. Types of fracture: (a) brittle; (b) ductile.
In brittle fracture, as shown in figure 4(a). failure occurs suddenly and

befor any appreciable plastic deformation takes place. The fracture follows the
paths between adjacent crystal planes. Brittle fracture generally occurs in
materials with the weakest atomic bonding, such as cast iron. glass and
concrete. Metals with body-centered-cubic and close-packed-hexagonal
structures are also susceptible to brittle fracture. Brittle fractures usually start
at some discontinuity in the material or component which results in a point of
stress concentration. This is not always the case and the 'pitting' caused by
corrosion, for example, can also act as 'stress raiser" in the metal.
Ductile fracture takes place at some stress figure above the yield point of the
material so that some plastic flow precedes failure. The resulting fracture is of
the 'cup and cone' variety shown in figure4(b), It is associated with face-
centered-cubic crystals such as those found in low-carbon steels. This type of
fracture occurs in destructive tensile test.
Since the fracture occurs in the plastic zone of the tensile test curve, it is
obviously the result of a design fault or severe overload. As previously stated,
6
the maximum working stress should not exceed 50 per cent of the yield stress
for the material, let alone reach the stress levels required to produce plastic
deformation.
The type of fracture produced is dependent mainly on the nature of the
material and its particular lattice structure. However, other factors can also
influence the onset of fracture, for example:
• The rate of application of stress.
• Environmental and temperature conditions (our previous example of ships
breaking up in the North Atlantic).
• The amount of cold working the material has received during any previous
processing.
• The shape of the component and whether or not it has sharp corners and
sudden changes of section.
• The surface finish of the components (machining marks are incipient cracks
(stress raisers)).
4. Corrosion
Corrosion and its prevention has been introduced in earlier lecture. The
selection of materials that are corrosion resistant is an important design
consideration. The conditions encountered by materials used on site or in the
hostile environment of a chemical plant are quite different to those encountered
in a domestic or office situation. It would be uneconomic to use the same level
of corrosion resistance and anti-corrosion coatings in all these situations. Each
application must be considered on its own merits.
Many of the problems associated with 'body-rot' in cars immediately after

the Second World War have been eliminated by better design to allow drainage
and ventilation of hollow box section members. Also anti-corrosion treatment
of the body panels before painting, and the use of improved paint systems,
have all added to the improved life of car bodies. Changes in materials have
also helped, with the use of high-impact polymers in those areas most
susceptible to spray and salt during winter motoring. Continuous adhesive
bonding has also eliminated the crevices left by spot welding, bolting and
riveting.
BATAAN HEROES MEMORIAL COLLEGE
ROMAN SUPER HIGH-WAY BALANGA CITY, BATAAN
In Partial Fulfillment for the Completion of

the Subject course in Engineering Materials
And Processes
Submitted by: Jose Franco D. Torres
Submitted to: Eng’r. R.C Lucas

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Engineering Materials

Introduction to Eng. Materials :

In the recent years studying the metallurgy science gave to humanity an

Figure 1. The electrical connector.

Another example as in figure 2 shows the connecting rod of a motor

Figure 2. The connecting rod of motor car engine.

Figure 3. classification of engineering materials.

Figure 4. Classification of ferrous metals.

1.2 Non – ferrous metals

Figure 5. Classification of non-ferrous metals and alloys.

2. Non – metallic materials

Figure 6. classification of synthetic materials.

 They combine good corrosion resistance with ease of manufacture

2.2 Non – metallic (Natural materials )

 Glass : This is a hardwearing, abrasion-resistant material with

 Ceramic: These are produced by baking naturally occurring clays

 Oils : Used as bearing lubricants, cutting fluids and fuels.

 Silicon : This is used as an alloying element and also for the

These and other natural, non-metallic materials can be classified as

Composite materials (composites )

Figure 7. Classification of natural materials.

Factors affecting materials properties:

Figure 8. Examples of (a) hot-working and (b) cold-working process.

Metal is hot worked or cold worked depending upon the

Metal Structure and Bounding in Materials :

Each atom is composed of a positively charged nucleus surrounded

Figure 1. Simple model of atomic structure for several elements :

We might infer that there is a maximum number of electrons that

Maximum number of electrons in an orbit = 2 n2

The number of electrons in the outermost shell, relative to the

Figure 3. Ionic bond .

As an example of this bond is the Sodium chloride (table salt) is

Figure 4. Covalent bond.

Solids with covalent bonding generally possess high hardness and

This cloud provides the attractive forces to hold the atoms

4. Van der Waal’s Force

(a) (b) (c)

There are some metals that are undergo a change of structure at

Two closely related features differentiate noncrystalline from

Figure 8. Difference in structure between (a) crystalline and (b) noncrystalline

2. Differences in melting and thermal expansion characteristics. It

The crystalline state :

Figure 9. Representation of part of a space lattice with a unit cell outlined.

The unit cell is the smallest parallel surfaces of the crystalline

For the Body-centered-cubic (BCC), it is obvious that the unit cell

The atomic packing factor [A.P.F]:

The volume of the unit cell is Vu = a3

There are 9 atoms 8 in the corners and 1 in the center of the

General Properties of Engineering Materials

Physical properties of materials

Figure 1. Electrical conductivity.

For example, metallic conductors of electricity all increase in

3. Melting temperature of material

Figure 2. Thermal conductivity.

Mechanical properties of materials

Figure 4. Tensile Strength

Figure 5. Toughness (Impact Resistance).

Figure 9. Stiffness (rigidity):

Figure 10. Elasticity.