Lecture 1 Fluid Mechanics
Lecture 1 Fluid Mechanics
Introduction
Fluid mechanics is the study of motions and forces in fluids since the nature and flow of most
materials handled in process industries is in fluid form. An understanding of the principles
governing the flow characteristics of these materials gives a chemical engineer/ process design
engineer a familiarity to the techniques to be used in designing storage and transportation
equipment of these materials. The concepts in fluid mechanics find wide application in the fields
of hydraulic design, aerodynamics, meteorology, particle dynamics, hydrology, reservoir
mechanics, multiphase flow et al.
A fluid may be defined as a substance that doesn‘t permanently resist distortion and hence will
change its shape. For this definition, gases, liquids and vapours are considered to have the
characteristics of fluids and to obey many of the same laws.
From the properties of fluids, the most that are required by a process/chemical engineer in an
assay or characterisation for calculations are:
Density
Viscosity
Surface tension
The study of fluid mechanics is subdivided into two main disciplines and we shall only deal
withthose areas of interest to processes in the coming lectures:
Fluid Statics–this deals with fluids under mechanical equilibrium as such they are under
no net motion
Fluid dynamics–this deals with fluids under motion.
This unit will be delivered through lectures and case study analysis of practical industrial
flowphenomena. As such the assessment will be on assignments (or small projects
whereossible),
tests and examinations following the criterion stipulated by International University of East
Africa University.
i. Viscosity
This is the measure of a fluid‘s resistance to flow. Fluids can be classified based on their
viscosity. An imaginary fluid of zero viscosity is called a Pascalfluid. The flow of a Pascal fluid
is termed inviscid (or non-viscous) flow. Viscous fluids are classified based on their
rheological (viscous) properties. These are detailed below:
1. Newtonian fluids, as described in the previous chapter, obey Newton‘s law of viscosity (i.e.,
the fluid shear stress is linearly proportional to the velocity gradient). All gases are considered
Newtonian fluids. Newtonian liquid examples are water, benzene, ethyl alcohol, hexane and
sugar solutions. All liquids of a simple chemical formula are normally considered Newtonian
fluids.
2. Non-Newtonian fluids do not obey Newton‘s law of viscosity. Generally they are complex
mixtures (e.g., polymer solutions, slurries, and so on).
a. Time-independent fluids are fluids in which the viscous properties do not vary with time.
b. Time-dependent fluids are fluids in which the viscous properties vary with time.
c. Visco-elastic or memory fluids are fluids with elastic properties that allow them to ―spring
back‖ after the release of a shear force. Examples include egg-white and rubber cement.
Shear stress vs. Rate of shear strain dv/dy. Each of these lines can be represented by
theequation
a. Pseudoplastic or shear thinning fluids are characterized by a fluid resistance decrease with
increasing stress (eg, polymers).
b. Dilatant or shear thickening fluids increase resistance with increasing velocity gradient or
applied stress. These are uncommon, but an example is quicksand.
c. Bingham plastics are fluids that resist a small shearing stress. At low shear stress these fluids
do not move. At high shear the fluids move.
The fluid just starts moving when sufficient stress is applied. This stress is termed the yield
stress. When the applied stress exceeds the yield stress, the Bingham plastic flows. Examples are
toothpaste, jelly, and bread-dough.
ii. Temperature:
All fluid properties are dependent upon temperature. For most fluids the viscosity is the property
that is most sensitive to temperature changes.
(a) Liquids
For liquids, as the temperature increases, the degree of molecular motion increases, reducing the
short-range attractive forces between molecules and lowering the viscosity. For many liquids,
this temperature dependence can be represented reasonably well by the Arrhenius equation
below;
( ⁄ )
.
.
b. Gases
The viscosity of a gas increases with increasing temperature. This is because gas molecules are
much farther apart, so the short-range attractive forces are very small. However, as the
temperature is increased, the molecular kinetic energy increases, resulting in a greater exchange
of momentum between the molecules and consequently a higher viscosity. The viscosity of gases
is not as sensitive to temperature as that of liquids, however, and can often be represented by the
equation:
where the temperatures are in degrees Rankine and TB is the boiling point of the gas.
iii. Density:
The density of both liquids and gases decreases with increasing temperature, and the density of
gases is much more sensitive to temperature than that of liquids.
The specific gravity of hydrocarbon liquids at 60oF is also often represented by the API gravity:
For gases, if the temperature is well above the critical temperature andthe pressure is below
thecritical pressure, the ideal gas law usually applies: