Amodel PPA Design Guide en PDF
Amodel PPA Design Guide en PDF
Amodel® PPA
Design Guide
SPECIALTY
POLYMERS
Table of Contents
Amodel® Polyphthalamide (PPA) The naming convention for polyamides uses the
number of carbon atoms in the monomers with the
Amodel® PPA resins were commercialized in 1991.
diamine component first. Thus, a polyamide made from
Polyphthalamide resin technology can produce a wide
hexamethylene diamine and adipic acid is called polyamide
range of polymers that includes both semi-crystalline
6,6 or nylon 6,6; the one made from hexamethylene
and amorphous resins. Since 1991, several base polymer
diamine and dodecanedioic acid would be nylon 6,12.
formulations have been commercialized to meet specific
industry needs. All of the commercial Amodel® products When an aromatic diacid is used instead of an aliphatic
are semi-crystalline. diacid, the nomenclature is modified to reflect the isomeric
form of the aromatic diacid, and the term polyphthalamide
The semi-crystalline grades of Amodel® PPA resins have
may be used to distinguish these polymers from those of
excellent mechanical properties, outstanding dimensional
solely aliphatic raw materials.
stability, exceptional elevated thermal performance, and
good processing characteristics. Amodel® resins bridge Polyamide 6,T produced by the condensation of
the cost/performance gap between the high-volume, hexamethylene diamine with terephthalic acid, has long
moderate-performance engineering resins, such as been recognized for its excellent dimensional stability, low
thermoplastic polyesters and aliphatic nylons, and the moisture absorption, high strength, and heat resistance.
low-volume, high-cost specialty thermoplastics, such The fundamental problem preventing its commercialization
as polyetheretherketone (PEEK). has been that its high crystalline melting point of 370 °C
(698 °F) is above its thermal decomposition temperature.
The Amodel® product portfolio contains well over 100
Therefore, it cannot be processed by most conventional
different grades. Each grade has been designed to
melt processing techniques, such as injection molding
have a unique balance of properties that are important
or extrusion. In addition, its melting point, among other
for specific application and processing requirements.
factors, complicates the polymerization process.
Applications for Amodel® PPA have been developed
in a wide range of industries including automotive/ The basic polyamide 6,T technology has been modified
transportation, industrial equipment, water handling, by adding comonomers to produce the Amodel® family
telecommunications, electrical/electronic, coatings, of polyphthalamide (PPA) resins which are composed of
composites, food service, and consumer goods. proprietary compositions of matter. Varying the amount
and nature of the comonomers leads to a family of resins.
This manual is intended to be an easy-to-use reference
All of these resins have melting points lower than polyamide
tool for designers and fabricators interested in Amodel®
6,T and exhibit rapid crystallization. The thermal properties
PPA as a solution to their material needs. It includes
of the Amodel® PPA base resins are shown in Table 1.1.
property data for select grades of the portfolio as well
as part design and processing recommendations. Table 1.1 A
model® PPA base resin properties
Chemistry Base Tg Tm
Amodel® resins are classified in the general chemical Resin [°C(°F)] [°C(°F)]
family known as polyamides. Polyamides may be A-1000 123 (253) 313 (595)
produced by the reaction of a difunctional organic acid A-4000 100 (212) 325 (617)
with a difunctional amine, or the self-condensation of A-5000 89 (192) 294 (561)
either an ω-amino acid or a lactam. Polyamides can A-6000 88 (190) 310 (590)
be produced from a wide variety of acids and amines.
Tg 1,200
Modulus [ GPa ]
1,000 150
800
100
Tm 600
400 50
200
0 0
Temperature 0 50 100 150 200 250 300
Temperature [ °C ]
When the temperature is raised, the modulus of
amorphous polymers generally decreases slowly until
the glass transition temperature (Tg ) is reached. At
temperatures above the Tg, the modulus decreases
rapidly. Therefore, amorphous thermoplastics are
rarely used at temperatures higher than their glass
transition temperature.
Figure 1.3 compares the glass transition temperatures Figure 1.4 Dimensional change vs. water
of Amodel® A-1000 resin and PA 6,6 at a range of immersion time
moisture contents. These materials absorb moisture
at different rates and they have different maximum 2.5
moisture adsorption amounts. The most useful and
2.0
Dimensional change [ % ]
practical comparison is achieved by plotting the Tg
versus the equilibrium moisture content at various
relative humidities. 1.5
Figure 1.3 E
ffect of moisture on Tg 1.0
300
140 A-1000 PPA 0.5
120 PA 6,6 250 A-1000 PPA
PA 6,6
100 0.0
200
80 0 1,000 2,000 3,000 4,000 5,000 6,000 7,000 8,000
Tg [ °F ]
150
Tg [ °C ]
60 Time [ hours ]
40 100
20
50
0
-20 0
-40 -50
0 10 20 30 40 50 60 70 80 90 100
Relative humidity [ % ]
Amodel® Resin Property Tables The base polymers are translucent white due to
crystallinity, and the natural color of a specific product will
Amodel® PPA resins are typically combined with
vary depending on the additives used. Most grades are
reinforcements, fillers, impact modifiers, flame retardants,
available in natural and black. Other colors can often be
colorants, and other additives to achieve a wide range of
provided. Please discuss your color requirements with
performance profiles. Currently the family contains over
your Solvay representative.
100 commercial grades. This document provides detailed
property information on 12 grades that were selected
to be representative of the product family. Your Solvay
representative can help you select the most cost-effective
material for your application.
Table 2.2 Relative ranking of selected properties for major Amodel® PPA grades(1)
(1)
Properties ranked from 1 to 10, with 10 being the highest
Method
A-1133 A-1145 A-6135 AS-4133
Property Units HS HS HN HS ASTM ISO
Thermal
Deflection temperature under load, 264 psi °C 285 287 291 300 D648
°F 545 549 556 572
Deflection temperature under load, 1.8 MPa °C 280 281 288 294 75AF
°F 536 538 550 561
Vicat softening temperature °C 303 304 301 314 D1525 306
°F 577 580 573 597
Melting point °C 313 310 310 327 D3418 11357-3
°F 595 590 590 620
Flammability, 3.2 mm (0.125 in.) bar HB HB HB HB UL-94
Electrical
Dielectric strength at 3.2 mm (0.125 in.) V/mil 533 584 — 510 D149
kV/mm 21 23 — 21
Dielectric strength at 1.6 mm (0.062 in.) V/mil 813 — — 813 D149
kV/mm 32 — — 32
Volume resistivity ohm-cm 1x1016 1x1016 — 1x1016 D257
15 15
Surface resistivity ohms 1x10 — — 1x10 D257
Comparative tracking index volts 550 550 — >600 D3638
Dielectric constant at 60 Hz 4.4 4.6 — 3.8 D150
Dielectric constant at 100 Hz 5.1 — — 4.6 D150
Dielectric constant at 10 6 Hz 4.2 4.4 — 3.6 D150
9
Dielectric constant at 10 Hz 3.7 — — 3.6 D150
Dissipation factor at 60 Hz 0.005 0.005 — 0.004 D150
Dissipation factor at 10 6 Hz 0.017 0.016 — 0.012 D150
Dissipation factor at 10 9 Hz 0.016 — — 0.013 D150
General
Specific gravity 1.48 1.59 1.45 1.45 D792 1183A
Moisture absorption, 24 hours % 0.2 0.1 0.3 0.3 D570 62
Mold shrinkage, flow direction % 0.4 0.2 0.6 0.5 D955 294-4
Mold shrinkage, transverse direction % 0.8 0.6 0.9 1.0 D955 294-4
The data sheets provided by material suppliers typically Figure 3.1 Typical stress/strain curve for
list short-term properties, and their primary utility is for Amodel® ET-1000
comparing similar materials. When using data sheets to
70 10
compare materials, it is very important to insure that the
same test methods have been used and that the data is 60
8
reported in similar units.
50
Stress [ MPa ]
Stress [ kpsi ]
The utility of short-term mechanical properties in design 40 6
is limited. Typically, the properties are measured using
molded test specimens that have been specifically 30
4
designed to yield reproducible results, under carefully 20
controlled environmental conditions, using specified 2
loading rates. These measurements often provide the 10
highest value obtainable for any property and material. 0 0
0 5 10 15 20
When parts are fabricated by a molding process they
Strain [ % ]
will likely contain a number of features such as stress
concentrations, weld lines, corners or other aspects
that may reduce strength. The strength of a material in
an actual component may also be reduced, or in some
cases enhanced, by reinforcing fiber orientation, relative
degree of crystallinity, or thermal history (annealing). In
addition, short-term properties do not provide any insight
regarding time-related effects or the influence of chemical
environments.
Figure 3.2 Typical stress/strain curve for The tangent method was used for the tensile data run by
Amodel® A-1933 ASTM D638 presented in this brochure.
Stress [ kpsi ]
yield or tensile stress at yield. The elongation achieved at
100 15 this point is called the elongation at yield, yield strain or
tensile strain at yield. As the test proceeds, the specimen
10 continues to elongate until rupture occurs. The stress level
50 at this point is called tensile strength at break, ultimate
5
tensile strength or tensile stress at break. Tensile strength
0 0 is defined as the greater of the measured stresses, which
0.0 5 1.0 1.5 2.0 could be either the stress at yield or the stress at rupture.
Strain [ % ]
Tensile property comparison
The initial portion of the stress/strain curve is also of Amodel® A-1133 HS resin has higher tensile strength
special interest because its slope relates to the stiffness at room temperature than 33 % GR polyamide (PA) 6,6,
or modulus of the material as shown in Figure 3.3. 30 % GR polyphenylene sulfide (PPS), and 30 % GR
polyetherimide (PEI), as shown in Figure 3.4. Even after
Figure 3.3 Secant and tangent methods for moisture conditioning, Amodel® PPA is stronger than the
estimating modulus other resins.
DAM 30
200 50% RH
Stress [ MPa ]
25
Tensile strength [ MPa ]
100 15
Stess/strain curve 10
Secant 50
Tangent 5
Strain [ % ] 0 0
A-1133 HS PA 6,6 PPS PEI
This figure shows that the strain is directly proportional
to stress up to a certain amount of stress. This region is
known as the “Hookean” or elastic region. The maximum
stress level that results in a proportional amount of strain
is known as the proportional limit.
10 1.5 100
8 10
50 A-1133 HS
1.0 A-4133 L
6 A-6135 HN
0 0
4 0 50 100 150 200
0.5
Temperature [ °C ]
2
Figure 3.8 Tensile modulus of 33 % GR PPA vs.
0 0.0
A-1133 HS PA 6,6 PPS PEI temperature
Temperature [ °F ]
This same comparison for tensile elongation is shown in 50 100 150 200 250 300 350
Figure 3.6. The tensile elongation of the resins is low due
to the glass fiber reinforcement. Moisture conditioning 14 2.0
the PA 6,6 results in an increase in elongation due to the 12
reduction in Tg.
10 1.5
0 0.0
3 0 50 100 150 200
Temperature [ °C ]
A-4133 L
8 A-6135 HN 8
Tensile properties for GR PPA vs. temperature
Figures 3.7 through 3.9 show the tensile properties of GR 6 6
grades of Amodel® PPA based upon A-1000, A-4000, and
A-6000 base resins from RT to 175 °C (347 °F). Amodel® 4 4
A-1133 HS has the highest strength and stiffness at room
temperature, but A-4133 L and A-6135 HN have better 2 2
strength and stiffness above 150 °C (302 °F).
0 0
0 50 100 150 200
Temperature [ °C ]
30
150
200 25 20
20 100 15
150
15
10
100
10 50
A-1133 HS 5
50 5
A-1145 HS
A-1160 HSL 0 0
0 0
0 50 100 150 200
0 50 100 150 200 Temperature [ °C ]
Temperature [ °C ]
2.5
20 3.0 15
2.0
2.5
15 10 1.5
2.0
10 1.5 1.0
5
1.0 0.5
5
0.5
0 0.0
0 0.0 0 50 100 150 200
0 50 100 150 200 Temperature [ °C ]
Temperature [ °C ]
8 1.2
The flexural modulus of elasticity is the ratio, within the
1.0
elastic limit, of the stress in the outermost fiber of the
6
object being stressed to corresponding strain. As in 0.8
tensile testing, the modulus is calculated from the slope of 0.6
4
the load deflection curve in the linear “Hookean” region.
0.4
Flexural testing provides information about the relative 2
0.2
strength and stiffness of materials when subjected
0 0.0
to bending loads. The material with the higher flexural A-1133 HS PA 6,6 PPS PEI
strength can endure higher bending loads without
fracture. Parts produced from a material with a higher
flexural modulus will deflect less when subjected
to a bending load than parts made of a lower
modulus material.
1.6
3.0
Flexural modulus [ Mpsi ]
20
Flexural modulus [ GPa ]
10 1.4
2.5
8 1.2 15
2.0
1.0
6 10 1.5
0.8
0.6 1.0
4 5
A-1133 HS 0.4 0.5
2 A-4133 L 0
0.2 0.0
A-6135 HN
0 0.0 0 50 100 150 200
Temperature [ °C ]
0 50 100 150 200
Temperature [ °C ]
AS-1566 HS
2.5
15 Figure 3.23 Shear strength of 30 % – 33 % GR resins
2.0
120
10 1.5 DAM
16
50% RH
1.0 100 14
Shear strength [ MPa ]
A-1133 HS
12
A-1145 HS
Compressive modulus [ Mpsi ]
Compressive modulus [ GPa ]
8
1.0
6
4
0.5
2
0 0.0
0 20 40 60 80 100 120 140 160
Temperature [ °C ]
140 DAM
2.5
120
Notch 2.0
radius 100
80 1.5
60
1.0
40
0.5
Clamp 20
0 0.0
Izod impact can also be run on un-notched specimens. A-1133 HS PA 6,6 PPS PEI
The applicable test methods are ASTM D4812 or ISO
180U. The major difference between these methods and
the notched methods is that the full width of the specimen
is used in the calculation.
14
12 600
600 10
10
400
400 8
5
6 200 AT-1001 L
ET-1000 HS
200 4 0 0
2 -50 -40 -30 -20 -10 0 10 20
0 0 Temperature [ °C ]
ET-1000 PA PA6 PC PC/PBT
HS 6,6
Charpy (supported beam) impact
Figure 3.30 Notch radius sensitivity of ET-1000 HS
Charpy is similar to Izod because a test specimen is
and PC
struck by a falling pendulum and the energy to break the
Notch radius [ mils ] specimen measured. The primary difference is that in the
0 5 10 15 20 Charpy test the specimen is supported at both ends and
1,000 struck in the middle, as shown in Figure 3.32. The test
methods used were ISO 179/1eA and 179/1eU.
800 15
Izod impact [ ft-lb/in ]
50% RH
Grade Condition N lb J ft-lb
12
1.5 AT-1001 L DAM 4,900 1,100 54 40
10
AT-1002 HS DAM 4,400 1,000 54 40
8 AT-1002 HS 50 % RH 4,000 900 47 35
1.0
6 AT-5001 DAM 4,400 1,000 54 40
AT-5001 50 % RH 4,000 900 50 37
4 0.5 ET-1000 HS DAM 4,670 1,050 54 40
2 ET-1001 L DAM 5,600 1,260 64 47
0 0.0
A-1133 HS PA 6,6 PPS PEI
Poisson’s Ratio
Falling weight impact properties Poisson’s ratio is a measure of the strain characteristics
ASTM D3763, High-Speed Puncture Properties of imposed on a material transverse to the applied load.
Plastics Using Load and Displacement Sensors, was Poisson’s ratio is the ratio of lateral strain to longitudinal
used to measure the practical toughness of Amodel® strain within the proportional limit. To illustrate, consider
polyphthalamide resins. a cylindrical bar subjected to tensile stress: the length (L)
increases and simultaneously its diameter (D) decreases.
In this test, an injection molded specimen is clamped
down over a 76 mm (3 in.) diameter hole and a weighted In this case, Poisson’s ratio (υ) would be calculated by:
plunger is dropped from a predetermined height to give it -ΔD
a predetermined impact velocity. The plunger assembly D
consists of a 12.7 mm (0.500 in.) diameter steel rod with υ=
ΔL
a hemispherical end. The plunger assembly is attached
L
to a load cell which measures the energy needed to cause
a sample to fail. Most plastic materials have a Poisson’s ratio between
0.3 and 0.5.
Specimens can fail in either a brittle or a ductile mode.
In a ductile failure mode, the specimen is permanently
deformed to the shape of the plunger, but remains in
one piece after the penetration by the plunger. In a brittle
failure mode, the specimen does not have sufficient
ductility to be deformed without failure, and therefore
breaks into two or more pieces when impacted by
the plunger.
The significance of data from creep tests is that they The results of the tensile creep testing at 125 °C (257 °F)
can be used to calculate the time dependent creep strain are shown in Figures 3.36 and 3.37; results for 175 °C
and creep modulus for use in stress calculations and to (347 °F) are shown in Figures 3.38 and 3.39.
determine the safe stress levels for specific time
and temperature conditions. If the creep tests are
conducted until failure occurs at various stress levels,
a creep rupture curve can be produced.
3.0 12
20
1.5
2.5 10
1.0 4
5 0.5
A-1133 HS 0.5 2
A-1145 HS A-1133 HS
0 0.0 A-1145 HS
0 0.0
1 10 100 1,000
1 10 100 1,000
Time [ hours ]
Time [ hours ]
Figure 3.35 Apparent modulus at 23 °C (73 °F) and Figure 3.38 Apparent modulus at 175 °C (347 °F)
34.5 MPa (5 kpsi) and 13.8 MPa (2 kpsi)
3.0 10
20 1.4
Apparent modulus [ Mpsi ]
Apparent modulus [ GPa ]
2.5 1.2
Figure 3.36 Apparent modulus at 125 °C (257 °F) Figure 3.39 Apparent modulus at 175 °C (347 °F)
and 13.8 MPa (2 kpsi) and 34.5 MPa (5 kpsi)
14 2.0 8
12 7 1.0
Apparent modulus [ Mpsi ]
10 1.5 6
0.8
5
8
1.0 4 0.6
6
3 0.4
4
0.5 2
2 0.2
A-1133 HS 1 A-1133 HS
A-1145 HS A-1145 HS
0 0.0 0 0.0
1 10 100 1,000 1 10 100 1,000
Time [ hours ] Time [ hours ]
The isochronous stress/strain curves for Amodel® Creep rupture envelopes were developed in accordance
A-1133 HS resin at 23 °C (73 °F), 125 °C (257 °F), and with ASTM D2990. Tensile specimens were 3.2 mm
175 °C (347 °F) are shown in Figure 3.40. (0.125 in.) thick injection molded ASTM D638 Type I
tensile bars. The environments were the same as in the
Figure 3.40 Isochronous stress-strain of A-1133 tensile creep testing above. The samples were loaded in
HS PPA tension using pneumatically actuated bellows to maintain
Tensile creep - A-1133HS indicated stress levels.
40
The tensile creep rupture envelopes for Amodel®
35 5 AS-1133 HS resin are shown in Figure 3.42 at 65 °C
30 (149 °F), 100 °C (212 °F), and 150 °C (302 °F).
4
25
Stress [ MPa ]
20 3
200
15 25
2
10 150
1 20
Stress [ MPa ]
Stress [ kpsi ]
5
100 15
0 0
0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 1.6
10
Strain [ % ]
50
65 °C ( 149 °F )
1 hr 23 °C 1 hr 125 °C 1 hr 175 °C® 5
Figure 10
3.41 shows 100 °C ( 212 °F )
hr 23 °C the same
10 hr information
125 °C for10
Amodel
hr 175 °C 150 °C ( 303 °F )
A-1145100
HS.hrAs
23 expected,
°C thehrmore
100 125 °Cglass reinforcement
100 hr 175 °C in 0 0
1,000 hr 23 °C 1,000 hr 125 °C 1,000 hr 175 °C
the compound, the better the creep resistance. 0.01 0.1 1 10 100 1,000 10,000
Time to rupture [ hours ]
Figure 3.41 Isochronous stress-strain of A-1145
HS PPA
Tensile creep - A-1145HS
40
35 5
30
4
25
Stress [ MPa ]
Stress [ kpsi ]
20 3
15
2
10
1
5
0 0
0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 1.6
Strain [ % ]
1 hr 23 °C 1 hr 125 °C 1 hr 175 °C
10 hr 23 °C 10 hr 125 °C 10 hr 175 °C
100 hr 23 °C 100 hr 125 °C 100 hr 175 °C Amodel® PPA Design Guide / 35
1,000 hr 23 °C 1,000 hr 125 °C 1,000 hr 175 °C
Flexural creep Figure 3.44 Apparent flex modulus at 14 MPa
Flexural creep was determined according to ASTM D2990 (2 kpsi) at 83 °C (181 °F)
using the three-point bending mode with a 50.8 mm (2 in.) 3.0
span. Test specimens were 127 mm x 12.7 mm x 3.2 mm ET-1000 400
PA 6,6
(5.0 in. x 0.5 in. x 0.125 in.) injection molded bars placed 2.5
1.4
Apparent modulus [ GPa ]
8
8 1.2
1.0 7 1.0 Apparent modulus [ Mpsi ]
Apparent modulus [ GPa ]
6 6
0.8
0.8
4 0.6 5 23 °C - 34 MPa ( 73 °F - 5 kpsi )
100 °C - 28 MPa ( 212 °F - 4 kpsi ) 0.6
AS-1133 HS 0.4 4
150 °C - 21 MPa ( 302 °F - 3 kpsi )
2
33% GR PA 6,6 0.2 3
A-1240 L 0.4
0 0.0 2
1 10 100 1,000 10,000 0.2
1
Time [ hours ]
0 0.0
Figure 3.44 compares the apparent flexural modulus 0.1 1 10 100 1,000
of Amodel® ET-1000 resin with that of unreinforced Time [ hours ]
and impact modified grades of PA 6,6 at 83 °C (181 °F)
and 14 MPa (2 kpsi). In most applications where Amodel® resin will be loaded
in a compressive manner, the load will be applied in the
direction transverse to flow direction and consequently the
fiber orientation. Therefore, the apparent moduli presented
here are representative of the material’s performance in
typical applications.
Stress [ kpsi ]
stress versus number of cycles at rupture. A smooth curve Stress [ MPa ]
is calculated that represents the best fit to the data. For 80 12
component design purposes, this S–N (stress–number 10
60 8
of cycles) curve provides strength values appropriate
40 6
for the components required life.
4
When designing a component that will be subjected 20
2
to cyclic loading, the establishment of fatigue strength 0 0
requirements is desirable. However, analysis of the fatigue 103 104 105 106 107
strength requirements is complicated by a large number Cycles to failure
of factors that may influence them. Some of these factors
include the following:
Figure 3.47 gives the fatigue behavior of Amodel® AS-1145
• Shape of the component HS resin at 110 °C and 170 °C (230 °F and 338 °F). As
• Stress concentration factors expected, raising the temperature reduces the amount
of cyclic stress that can be endured.
• Rate of load application
• Any temperature change caused by load application A good example of an application involving cyclical stress
is a gear. As the driving gear causes the driven gear to
• Type of stress induced by load, that is, tensile,
rotate, each tooth is subject to stress. This is then followed
compressive, or shear, etc.
by a period of time at low or zero stress. In designing a
• Environmental factors, such as, chemicals, radiation,
gear tooth, the appropriate strength criteria is the fatigue
ambient temperature
endurance limit of the material at the operating conditions
• Residual stresses of the gear.
• Duty cycle
• Desired component life
Stress [ kpsi ]
6 Amodel® polyphthalamide resins have significant amounts
40
of aromatic character in the polymeric “backbone” and
30 this causes them to absorb much less moisture than
4
aliphatic polyamides such as PA 6,6 and PA 6. As a result,
20
the dimensions, strength, and stiffness of Amodel® parts
2
10 will be significantly less affected by the absorption of
moisture than traditional aliphatic PA parts. Since moisture
0 0
is ubiquitous, knowledge of the effects of moisture on the
103 104 105 106 107
Cycles to failure properties of a material is critical to the design engineer
trying to meet end use requirements.
After all of the calculations have been made, the part
Significance of moisture absorption
design can be modified to best utilize the properties
of the selected material. Conversely, the material grade When a polymer absorbs atmospheric moisture, a number
can be modified to best suit the application requirements. of changes may occur. Obviously, the part weight will
An extremely useful tool to verify a design is to perform increase and this weight increase is typically used to
Finite Element Analysis (FEA). In FEA, the part is measure the amount of moisture absorbed. Additionally,
electronically modeled and a computer program is used there may be some dimensional changes and generally
to simulate the anticipated loads and stresses. The the parts become larger. The presence of reinforcing fillers
resulting strain levels can be evaluated and, if necessary, such as fiberglass may result in anisotropic dimensional
part design or material changes can be made. It is much change due to the fact that the fibers align themselves
easier to make changes to the FEA model than to a in the direction of polymer flow as the resin fills the tool.
fabricated part or tooling. Similar to mold shrinkage values, dimensional changes
due to moisture absorption are often reported in flow and
Even after calculations and FEA’s have been performed, transverse directions.
the best way of evaluating a material for a component
subject to dynamic stresses is actual prototype testing. Mechanical properties may also be affected by moisture
Prototype parts can be machined from available stock absorption. Generally, a slight decrease in physical
shapes and subject to performance testing under the properties such as tensile and flexural strength are seen.
requirements of the application. Stock shapes are usually The respective moduli also decrease slightly. Impact
available as extruded slabs or rods and generally exhibit strength values tend to increase slightly since the presence
slightly lower mechanical properties than the injection of moisture can tend to plasticize the polymer. Since water
molded part. Additionally, the machining operations is a conductor, absorbed moisture can have a negative
usually induce stresses that would not normally be effect on the dielectric properties of a molded part.
present in an injection molded part. As a result, a Manufacturers of polymers that absorb moisture usually
successful prototype test imparts an extremely high publish two sets of data, one listing test results on test
confidence level in the reliability of the design. specimens that have no absorbed moisture, commonly
referred to as “Dry–As Molded” (DAM), and a second set
of data that is generated on test specimens that have
been allowed to come to an equilibrium weight in a 50 %
Relative Humidity environment, known as “50 % RH”.
Polymers like PA 6 and PA 6,6 absorb moisture relatively
quickly and reach equilibrium in a 50 % Relative Humidity
environment quickly. Providing 50 % RH data for these
materials is fairly easy and extremely relevant to design,
as will be understood in the subsequent discussion.
FD @ 100% RH
100 °C (212 °F) and decreases further with moisture 0.5
TD @ 50% RH
absorption. FD @ 50% RH
0.4
Dimensional change [ % ]
1.0
Figure 3.52 Dimensional change of 40 % mineral AS-1133 HS - TD
AS-1133 HS - FD
Filled PPA 0.8
33% GR PA 6,6 - TD
33% GR PA 6,6 - FD
0.6 0.6
TD @ 100% RH
Dimensional change [ % ]
FD @ 100% RH
0.5 0.4
TD @ 50% RH
FD @ 50% RH
0.4 0.2
FD = flow direction
0.3 TD = transverse direction
0.0
0 2 4 6 8 10 12 14
0.2
Time [ month ]
0.1
FD = flow direction
Amodel® resin absorbs moisture much more slowly
TD = transverse direction
0.0 than PA 6,6, because the diffusion coefficient at room
0 2 4 6 8 10 12 14 temperature of water in PA 6,6 is approximately five times
Time [ month ] larger than that of Amodel® resins. Therefore, for these
plaques, PA 6,6 reaches equilibrium in approximately four
Dimensional change compared to PA 6,6
months while Amodel® AS-1133 HS resin requires more
Figure 3.53 compares the dimensional change due than two years.
to moisture absorption of Amodel® AS-1133 HS resin
with that of 33 % glass reinforced PA 6,6 at 100 % RH.
To ensure a valid comparison, both resins were molded
under conditions that promote maximum crystallinity.
In the case of the Amodel® resin, a mold temperature
of 135 °C (275 °F) was used. For the PA 6,6, the mold
temperature was 93 °C (200 °F). Plaques with a thickness
of 3.2 mm (0.125 in.) were exposed to 100 % RH at room
temperature.
Deflection temperature [ °F ]
560
Plastics Under Flexural Load and ISO 75, Plastics - 290
550
Determination of Temperature of Deflection Under 285
Load. These tests are commonly referred to as Heat 540
280
Distortion Temperature (HDT) or Deflection Temperature 530
under Load (DTUL). Both tests are similar in that the 275
test specimen is supported at two points while a load 270 520
is applied to the center. The temperature is increased 265 510
at a constant rate until the specimen deflects a specified
260 500
amount as indicated by a dial micrometer. 121 °C 135 °C Annealed
Mold temperature 2 hours @ 160 °C
Although details such as specimen geometry, deflection Thermal history
endpoint, specimen orientation, and distance between
the supports are different for these methods, the desired Deflection temperature measures modulus at temperature
stress levels for both methods includes a loading of measurement. Classical stress/strain analysis indicates
1.8 MPa (264 psi) and 0.45 MPa (66 psi). When comparing that the ASTM D648 test actually measures the
data from multiple sources, it is important to verify that temperature at which the flexural modulus is 240 MPa
the same test method was used for all the data being (35,000 psi) when the applied stress is 0.45 MPa (66 psi),
compared. In the product property tables starting on or 965 MPa (140,000 psi) when the applied stress is
page 9, data collected using both methods is listed. 1.8 MPa (264 psi). Because the test method directs that
Examination of the data will reveal a considerable amount the indicator be re-zeroed after five minutes, any creep
of difference between the values for some grades. strain that occurs in the first five minutes is effectively
Certain test parameters can have a significant influence subtracted from the endpoint strain lowering the actual
upon the results obtained in this test. The designer modulus at the end point of the test. The initial modulus
should be certain that data from multiple sources are can be related to the creep strain.
comparable. The most common and critical error is to
compare the results from testing performed at 1.8 MPa
(264 psi) with results obtained from testing at 0.45 MPa
(66 psi). All Amodel® resins are tested at 1.8 MPa,
Deflection temperature [ °F ]
Temperature [ °F ]
4 1.0
100 200 300 400 500 600
0.8 6
3 1.4
0.6
5 1.2
0.4
4 1.0
1 0.2
0.8
3
0 0.0
0.6
0 50 100 150 200 250 300 350 2
Temperature [ °C ] 0.4
1 0.2
Figure 3.58 Amodel® A-4000 PPA, specific heat
vs. temperature 0 0.0
0 50 100 150 200 250 300 350
Temperature [ °F ] Temperature [ °C ]
100 200 300 400 500 600
6 1.4
5 1.2
Specific heat [ Btu/lb °F ]
Specific heat [ J/g °C ]
4 1.0
0.8
3
0.6
2
0.4
1 0.2
0 0.0
0 50 100 150 200 250 300 350
Temperature [ °C ]
60 100,000
AS-1133 HS
Time to tensile strength half-life
33% GR PA 6,6
40
20 10,000
0
250 300 350 400 450 500 550 600 650 1,000
Temperature [ °C ]
Thermal aging
100
Nearly all polymeric materials exhibit some loss of 150 160 170 180 190 200 210 220 230
performance properties after long-term exposure to Temperature [ °C ]
elevated temperatures. While some polymers are more
stable than others, the property loss is typically a function
of both exposure time and temperature. Because the
property losses result from both oxidative attack and
thermal degradation, the term “thermal oxidative stability”
is frequently used.
33% GR PA 6,6
temperatures. Periodically specimens are removed and
tested. The results for each aging temperature are plotted
10,000
on a time versus property graph, until the property being
measured has declined to 50 % or less of its initial value.
This combination of time and aging temperature can be
1,000 referred to as the “half-life” for that property, material,
and thickness.
UL 746A specifies that the test be run on two sets A-1145 HS Dry 1 x 1016 –
15
of specimens: one set conditioned for 48 hours at A-1145 HS 50 % RH 2 x 10 –
16 15
23 °C (73 °F) and 50 % relative humidity; and the other AS-4133 HS Dry 1 x 10 1 x 10
conditioned for 96 hours at 35 °C (95 °F) and 90 % AS-4133 HS 50 % RH 5 x 1014 –
relative humidity. AT-1002 HS Dry 1 x 1016
8 x 1013
14
Volume resistivity is particularly sensitive to temperature AT-1002 HS 50 % RH 7 x 10 2 x 1013
15
changes as well as changes in humidity. Data on different AT-5001 Dry 4 x 10 4 x 1015
materials are comparable only for equivalent moisture AT-5001 50 % RH 2 x 1015 2 x 1015
content and temperatures. Materials with resistivities AT-6115 HS Dry 1 x 1016 1 x 1015
above 108 ohm-cm are considered insulators, while those AFA-6133 V0 Z Dry 1 x 1016
1 x 1015
with values of 103 to 108 ohm-cm are partial conductors.
A-1240 L Dry 9 x 1015 –
Table 3.32 High-current arc ignition performance Table 3.34 UL 746A property PLC for Amodel® PPA
level categories grades
Value Range [Sec.] Grade mm(1) HWI HAI HVTR CTI
< > Assigned PLC A(AS)-1133 HS 0.80 0 0 4 0
(2)
120 0 AT-6115 HS 0.80 0 0 1 0
120 60 1 AT-6130 0.80 4 0 1 0
60 30 2 AS-1566 HS 0.80 – 0 0 0
(2)
30 15 3 A-1340 HS 0.80 0 0 1 1
15 7 4 AS-4133 HS 0.80 0(2) 0 1 0
7 0 5 AFA-4133 V0 Z 0.75 0 0 1 1
AFA-6133 V0 Z 0.75 0 0 1 1
Tensile
Conc. Temperature Strength Change in Change in
Reagent [%] [°C (°F)] Resin Rating Retained [%] Length [%] Weight [%]
Ammonium 10 23 (73) Amodel® AS-1133 HS E 96 0.1 0.8
hydroxide
33 % Glass PA 6,6 A 61 0.2 4.5
30 % Glass PET E 95 0.2 0.4
Deionized water 100 93 (200) Amodel AS-1133 HS
®
A 69 0.2 3.4
33 % Glass PA 6,6 A 62 0.2 5.0
30 % Glass PET U 19 0.0 2.4
Sodium chloride 10 23 (73) Amodel AS-1133 HS
®
E 97 0.1 2.1
33 % Glass PA 6,6 A 67 0.2 3.3
30 % Glass PET E 98 0.0 0.3
Zinc chloride 50 93 (200) Amodel AS-1133 HS
®
A 66 0.1 4.8
33 % Glass PA 6,6 U 0 * *
30 % Glass PET A 54 -0.1 0.6
Sulfuric acid 36 23 (73) Amodel AS-1133 HS
®
E 92 0.0 1.8
33 % Glass PA 6,6 U 0 * *
30 % Glass PET E 94 0.0 0.3
Sodium hydroxide 10 23 (73) Amodel AS-1133 HS
®
E 93 0.0 1.6
33 % Glass PA 6,6 A 62 0.0 3.1
30 % Glass PET A 70 0.0 -4.2
Sodium 5 23 (73) Amodel® A-1133 HS E 94 0.0 1.4
hypochlorite
33 % Glass PA 6,6 A 57 0.0 -1.5
30 % Glass PET E 94 0.0 0.4
* Attacked
Tensile
Temperature Strength, Change in Change in
Fluid [°C (°F)] Resin Rating Retained [%] Length [%] Weight [%]
50 % Antifreeze 104 (220) Amodel® AS-1133 HS A 77 0.2 5.6
solution 33 % Glass PA 6,6 A 54 0.3 8.3
30 % Glass PET U 0 * *
Brake fluid 49 (120) Amodel AS-1133 HS
®
E 99 0.0 0.4
33 % Glass PA 6,6 E 105 -0.1 0.2
30 % Glass PET E 97 0.0 1.0
Diesel fuel 23 (73) Amodel AS-1133 HS
®
E 98 0.0 0.1
33 % Glass PA 6,6 E 100 0.0 0.3
30 % Glass PET E 100 -0.1 0.0
Gasohol (10 % 23 (73) Amodel AS-1133 HS
®
A 86 0.0 1.4
ethanol) 33 % Glass PA 6,6 A 65 0.1 3.5
30 % Glass PET E 93 -0.1 0.7
Hydraulic fluid 49 (120) Amodel AS-1133 HS
®
E 92 0.0 0.3
33 % Glass PA 6,6 E 103 0.0 0.3
30 % Glass PET E 105 -0.1 0.1
JP-4 jet fuel 23 (73) Amodel AS-1133 HS
®
E 95 0.0 0.4
33 % Glass PA 6,6 E 100 0.0 0.3
30 % Glass PET E 100 0.0 0.1
Motor oil 121 (250) Amodel AS-1133 HS
®
E 100 0.0 0.1
33 % Glass PA 6,6 E 106 0.0 -0.2
30 % Glass PET E 91 -0.1 -0.6
Power steering fluid 49 (120) Amodel AS-1133 HS
®
E 97 0.0 0.1
33 % Glass PA 6,6 E 106 0.0 0.2
30 % Glass PET E 108 0.0 0.0
Transmission fluid 121 (250) Amodel AS-1133 HS
®
E 97 0.0 0.1
33 % Glass PA 6,6 E 105 -0.1 -0.2
30 % Glass PET A 64 0.1 -0.5
Unleaded gasoline 23 (73) Amodel® AS-1133 HS E 96 0.1 0.0
33 % Glass PA 6,6 E 99 0.1 0.1
30 % Glass filled PET E 99 0.0 0.1
* Attacked
In this section, basic design principles and general Table 4.1 Design benefits of Amodel® resin over
recommendations are presented to assist the design metals
engineer in designing plastic components that meet
the cost/performance requirements of their applications. Amodel® Resin
Characteristics Benefit in Design
Guidelines are given on the effects of stresses caused
by assembly, temperature changes, environmental factors, Amodel resins are fabricated
®
Ribs, bosses, or cored
by the injection molding sections can be readily
and time as it relates to creep. process, which allows incorporated.
substantial design freedom
Of the various materials available to a design engineer,
Snap fits can be molded in,
thermoplastics offer the greatest variety, versatility
simplifying assembly.
and freedom of design. Plastics can be translucent or
Eliminate many secondary
opaque, rigid or flexible, hard or soft. Plastic materials are operations such as drilling,
available that provide a wide range of chemical resistance, tapping, boring, deburring,
from chemically inert to selective solubility in certain and grinding.
environments. Broad versatility is also available for other Metal inserts can be easily
properties like strength, stiffness and impact resistance, used where necessary to
optimize part strength.
lubricity and thermal capability. Blends and alloys are
possible that further increase the material choices for a Features from several metal
parts of an assembly may be
particular application. combined into a single part,
simplifying assembly and
At times, designing with plastics may appear more reducing cost.
complicated than with metals. But the diversity of
Amodel® resins Parts may be joined with
products, conversion processes, and secondary are thermoplastic ultrasonic or vibration
operations (welding, inserts, printing, painting, metallizing) welding rather than fasteners.
available with plastics gives the designer unprecedented Color may be molded-in
freedom as shown in Table 4.1. rather than added afterward
as paint.
A designer may be tempted to make a plastic part that Amodel® resins resist Parts will not rust, and resist
merely duplicates the dimensions of a metal part without chemicals corrosion.
taking advantage of the versatility of the plastic material
or the design freedom offered. This approach can lead
to inefficient designs or parts that are difficult to produce,
or whose performance is less than optimal.
F
FL F FL
σ= σ=
4Z Z
( at load ) ( at support )
FL3 FL3
Y= L Y=
48EI Y 8EI
L Y
( at load ) ( at load )
5FL3 FL3
Y= Y=
384EI 8EI
L L
( at center ) Y ( at support )
Y
F F ( total load )
½L
FL Y FL
σ= σ=
8Z 12Z
( at supports ) ( at supports )
FL3 FL3
L Y Y= Y=
192EI L 384EI
( at load ) ( at center )
Rectangular I-beam
t A = bd – h (b – t )
A = bd
d
d c=
c= 2
na 2
d
d bd3 – h3 (b – t )
bd3 na h I=
c I= 12
12 c
bd3 – h3 (b – t )
bd2 s Z=
Z= 6d
b 6
b
Circular H-beam
πd2 A = bd – h (b – t )
A= s h
4 b
c=
d 2
c=
na d 2 2sb3 + ht3
b na I=
πd4 12
c I= c
64
2sb3 + ht3
Z=
πd3 t 6b
Z= d
32
π ( d o2 – d i 2 ) A = b1d1 – b2d2
A=
4 d1
c=
d 2
c= o na d1
na di do 2
d2 b1d13 – b2d23
c b2 I=
c π ( d o4 – d i 4 ) 12
I=
64
b1d13 – b2d23
Z=
π ( d o4 – d i 4 ) b1 6d1
Z=
32do
s A = bs + ht A = bd – h (b – t )
b s h
2b2s + ht2
c=b–
d2t + s2 ( b – t ) 2A
na c=d– c
2 ( bs + ht ) t
d na 2b3s + ht3
b I= – A ( b – c )2
h c 3
I
Z= I
c Z=
c
t
d
tc3 + b ( d – c )3 – ( b – t ) ( d – c – s )3
I=
3
Selecting one case, for example, both ends fixed with a dAmodel = 3 3.25 ( 2.54 )3 = 3.76 mm ( 0.148 in. )
uniformly distributed load, the deflection is determined by:
or 48 % thicker than the magnesium part. However, ribs
FL3
Y= can be used to effectively increase the moment of inertia
384EI
as discussed in the next section.
Therefore, to equate the stiffness using two different
Adding ribs to maintain stiffness
materials, the deflections are equated as follows:
In the last section, it was determined that if a metal
FL3 FL3 part were to be replaced with a part molded of Amodel®
=Y=
384EI metal
384EI plastic AS-1145 HS resin, a part thickness of 3.7 mm (0.148 in.)
would be required to equal the stiffness of a 2.5 mm
Since the load and length are to remain the same, the FL3 (0.100 in.) thick magnesium part.
becomes a constant on both sides of the equation and
By incorporating ribs into the Amodel® design, the wall
what remains is:
thickness and weight can be reduced very efficiently,
Equation 1 yet be as stiff as the magnesium part.
[ EI ] metal = [ EI ] plastic
The moment of inertia for the plate design is: Figure 4.4 Cantilever beam, bending load example
F = 10 kg ( 22.0 lb )
bh3 25.4 × ( 3.76 )3
Iplate = = = 112.5 mm4 ( 2.70 × 10-4 in4 ) d = 6 mm ( 0.24 in )
12 12
Figure 4.3 A
dding ribs to increase stiffness
From Figure 4.1 on page 63, the deflection of a
1.9 mm ( 0.075 in ) cantilever beam is given by:
FL3
Y=
3EI
12.7 mm ( 0.50 in ) where I, the moment of inertia, as shown in Figure 4.2 is:
bd3
I=
12
25.4 mm ( 1.00 in ) Calculating the moment of inertia for this example gives:
2.54 mm ( 0.100 in ) ( 25 )( 6 )3
I= = 450 mm4 ( 1.081 × 103 in4 )
12
Therefore, the ribbed design will be 9.5 times stiffer than
The data sheet for Amodel® A-1133 HS resin gives
the Amodel® plate design or the original magnesium part
11.6 GPa (1.68 Mpsi) for the flexural modulus. Using
that was 2.5 mm (0.100 in.) thick.
this value and the equation previously cited, the short-term
The same rib having half the height would still produce room temperature deflection can be calculated by:
a part twice as stiff as the magnesium part. The ribbed
( 10 kg × 9.8066 )( .1 m )3
design shown requires placing a rib every 25 mm (1 in.) Y=
3( 11.6 × 109 Pa )( 4.5 × 10-10 m4 )
of section width.
Y = 6.3 mm ( 0.25 in )
2.6
Stress concentration factor
2.4
2.2 For example, the change in length of a material when
2.0 exposed to a change in temperature is given by:
1.8 Δ L = L ( TF − TO ) α
1.6
Where:
1.4 Δ L = change in length
L = original length
1.2
α = coefficient of thermal expansion
1.0 TF = final temperature
0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 TO = initial temperature
Radius / thickness ratio
Torque [ in-lb ]
40
4
F
σ= 30
Ap 3
2 20
Loss of Bolt Tightness Due to Creep A-1133 HS
1 33% GR PA 6,6 10
When threaded metal fasteners are used to retain or 30% GR PA 6,6
secure plastic parts to an assembly, and the assembly 0 0
is subjected to changes in temperature, the difference 20 40 60 80 100 120
between the thermal expansion coefficients of the metal Temperature [ °C ]
and the plastic can cause problems. When a threaded
fastener is tightened, the fastener is elongated slightly and The smaller difference in thermal expansion results in
a compressive stress is generated on the substrate. This lower induced stress due to the compressive strain
compressive stress maintains the tightness of the bolt. caused by the thermal excursion in the constrained part.
This translates to lower creep and therefore better torque
When the assembly is heated, both the plastic part and retention for such bolted assemblies.
the metal fastener will expand. The plastic part, however,
is constrained by the metal fastener, and cannot expand.
This results in increased compressive stresses in the
plastic and a corresponding increased tendency for
compressive creep or stress relaxation to occur. The
relaxation of the compressive stress will result in reduced
torque retention in the bolts.
The allowable interference between a shaft and a hub A press fit can creep or stress relax over time. This could
can be determined by using the general equation: cause a decrease in the retention force of the assembly.
Therefore, testing the assembly under its expected
operating conditions is highly recommended.
SdDs F + υh 1 – υs
I= +
F Eh Es
2
Ds
1+
Dh
F=
2
Ds
1–
Dh
Where:
I = Diametrical interference
Sd = Working stress
Dh = Outside diameter of the hub
Ds = Diameter of the shaft
Eh = Modulus of the hub material
Es = Modulus of the shaft material
υh = Poisson’s ratio of the hub material
υs = Poisson’s ratio of the shaft material
F = Geometry factor
Figure 4.10 illustrates the basic boss design for use with
self-tapping screws.
t
0.7 t
bd2
Z= and
6
b bd3
I=
12
d
Therefore:
L
Y FLd
σ=
2I
Each cantilever arm must deflect a distance “Y” in order
to be inserted. The key to proper snap design is to not The deflection of the beam, Y, is given by:
exceed the strain/stress limits of the material being used.
A snap fit design that has been used for a ductile, low FL3
Y=
modulus plastic will probably not be suitable for a highly 3EI
reinforced, very rigid plastic.
Equation 1
Figure 4.15 Snap fit design using tapered beam
L
3YEI
F=
L3
σ σ
E= and therefore ε =
ε E
FLd
ε=
2EI
For example, if the beam thickness has been gradually
Using the relationship of equation 1 and substituting reduced to half its fixed end thickness; the ratio of hL
for F in equation 2 the relationship between strain to h0 would be 0.5 and K (from Figure 4.16) would be 1.6.
and deflection is derived: Therefore, the maximum strain and the corresponding
stress would be multiplied the reciprocal of K, 0.625.
Equation 3 The strain will be reduced by about 40 % of the strain
of a constant thickness cantilever beam design with
3Yd
ε= equal deflection.
2L2
Figure 4.16 Proportionality constant (K) for tapered
This equation allows the designer to calculate the strain
beam
required from the maximum deflection of a design.
Table 4.2 summarizes maximum strain recommendations 2.4
for several grades of Amodel® resins.
Proportionality constant [ K ]
2.2
Once a suitable grade of Amodel resin has been
®
2.0
selected, the basic equations can be used to find the load,
1.8
F, needed to deflect the cantilever the required amount.
1.6
In a cantilever snap fit, the stress and strain are maximum
at the base of the cantilever and become proportionately 1.4
lower toward the tip where the load is applied. In fact 1.2
the stress and strain at any point can be calculated by
1.0
substituting a different L, the distance from the load
0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0
toward the fixed end. Therefore, if the cantilever thickness
Ratio of hL to hO
was gradually reduced from fixed end to tip, the beam
will be able to deflect more than in the fixed thickness
cantilever without incurring higher maximum stresses. In
this way, the capability of the material can be maximized.
Wall Thickness
In general, parts should be designed with the thinnest
wall that will have sufficient structural strength to support
the expected loads, keep deflection within design criteria
limits, have adequate flow, and meet flammability and
impact requirements. Parts designed in this manner will
have the lowest possible weight, and therefore the lowest
material cost, and the shortest molding cycle.
Poor Sharp More draft should be used for deep draws or when cores
are used. Textured finishes increase draft requirements by
a minimum of 1° per side for each 0.025 mm (0.001 in.) of
texture depth.
Good Tapered
Best Gradual
T
I.D.
0.3 T T
30° - 45°
Interference
The spin welding method uses frictional heat to join two The specimens used for the spin weld testing were
cylindrical or spherical mating parts. While one half is held injection molded cups with an interference joint design.
stationary in a nest fixture, the mating part is spun rapidly Excellent weld strength was obtained using this method.
against it. Friction at the interface raises the temperature
Because the welding condition settings were machine-
of the material until melting occurs. When the spinning
specific, they are not generally useful in setting a starting
action is stopped, the parts are held under pressure
point. Rather, it was observed that as forge pressure and
until cooled. Obviously, this welding method is limited to
angular velocity were increased, weld strength increased
parts with circular geometry at the joint. The advantage
up to a maximum and then decreased when an excessive
obtained through spin welding is the increased dispersion
amount of either pressure or velocity were applied. The
of material at the joint compared to other techniques. This
values for these parameters are strictly dependent on
allows for the development of hermetic seals and reduces
the part geometry and therefore they are not noted here.
the tolerance requirements on the joint geometry.
The explanation of the observed phenomena is that when
a weld was made with too high of a forge pressure, the
spinning motion was stopped too rapidly and not enough
polymer melted and flowed to create a sound joint. In
the other extreme, a high angular velocity and a low
forge pressure, the top part essentially sat on top of the
bottom part and freely rotated without being forced into
the interference fit. Thus, to assure a good joint, a welding
condition must be found so both melting and forging
occurs.
700
Lap shear [ psi ]
W/5 4 600
500
3 400
The ultrasonic welding machine used for this testing 2 300
was a Branson Model 910 M microprocessor-controlled 200
1
machine. With this unit, it is possible to adjust the amount 100
of ultrasonic energy that is applied to the sample. For 0 0
23 °C -34 °C 82 °C Promptly After
testing, the output from the booster was fed to near and ( 73 °F ) ( -30 °F ) ( 180 °F ) 24 hours
far field horns. The samples used were similar to the
injection molded cup used for the spin welding evaluation.
Aluminum fixtures held the parts in place and a butt weld
joint configuration was employed.
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