Lec.1 TP
Lec.1 TP
Lec.1 TP
FACULTY OF ENGINEERING
SORAN UNIVERSITY
Catalog Description: The course covers basics and applications of fluid mechanics (statics; mass, energy, and momentum
balances; laminar and turbulent flow, Reynolds number, Moody diagram; flow of non-Newtonian fluids; multi-phase flow; flow
in porous media, non-Darcy flow), and of heat transfer (heat conduction, convection, heat exchangers). It also emphasizes
analogies and similarities within mass, energy and momentum transport.
Topics Covered:
Textbook Required: Noel de Nevers: Fluid Mechanics for Chemical Engineers, McGraw-Hill. 2004
The careful application of this equation is necessary to most fluid-mechanics problems. Naturally we can divide by time and find
The mass balance has several other names, which are in wide use: principle of conservation of mass, continuity equation,
continuity principle, and material balance. They all mean exactly the same thing as mass balance, namely, that mass obeys
the general balance equation, with no creation or destruction.
of any measurable property of the system at any point is zero. Thus, if we write the balance equation for some measurable
quantity such as mass and divide by dt to find the rate form, then the left-hand side (the time rate of mass increase within the
system) must be zero, because at every point in the system the mass contained is not changing with time.
This is the familiar "flow in equals flow out" idea, which is true only for steady state, with no creation or destruction.
Example 3.2. For the pot-bellied stove of Example 3.1 we now make a steady-state carbon dioxide balance. By chemical analysis
we find that the amount of carbon dioxide in the natural gas and in the air is small enough to ignore; so, omitting the unnecessary
terms from Eq. 3.2, we find
General balance equation for some time period
Chemical analysis of the exhaust gas indicates that it contains considerable carbon dioxide, so the mass flow rate out is not
negligible. Thus, for this equation to be satisfied, there must be significant creation minus destruction of carbon dioxide in the
stove; i.e., carbon dioxide is formed by combustion in the stove. In this case, the destruction term is negligible
If we made a similar balance for natural gas, the destruction term would be approximately equal to the mass-flow-in term. In the
field of chemical reactions, the creation and destruction terms are very important and cannot be ignored.
Consider the steady-state flow of some fluid in a pipe of varying cross section (see
Fig. 3.2). If we apply the steady-state mass balance equation to the system shown,
we find
Mass flow in at point 1= mass flow out a point 2
In general, the velocity is not the same at every point in a cross section of pipe; it is faster near the center than at the walls.
Therefore, to calculate the total flow in across the system boundaries at point 1, we break up the area across which the flow
is entering into small subareas A, over each of which the flow is practically uniform:
Here the individual elements of area must be taken perpendicular to the local flow velocity. For flow in a pipe or channel this is
no problem, because the flow is all in one direction, and the area we normally consider is one perpendicular to the flow. If we
take the limit as each subarea becomes infinitely small, the term on the right becomes the integral, over the entire system
boundary at point 1, of V dA. Therefore, the steady-state mass balance for the system in Fig. 3.2 is
In most industrial flows in pipes or channels, the velocity is practically constant across the entire cross section of the pipe or
channel (except in a very thin layer near the pipe or channel wall). The density and velocity of these flows may be considered
constant across the cross section, and then the integrations in Eqs. 3.13 and 3.14 can be easily performed, giving
The mass crossing the boundary per unit time is called the mass flow rate. Normally it is measured in kilograms per second or
pounds-mass per second and given the symbol
For liquids at temperatures well below their critical temperature, the changes in density with moderate temperature and pressure
changes are small. Therefore, for liquids we can divide the density out of Eq. 3.15, finding
Mass divided by density equals volume; therefore the constant in this equation(the mass flow rate divided by the density) is the
volumetric flow rate, usually measured in cubic feet per second or cubic meters per second and given the symbol Q!
We choose as our system the tank up to the pump inlet. For this system the mass balance gives
where Vsys is the volume of the system, which does not change. Thus,
Furthermore,
For low-pressure gases at constant temperature, the densities are proportional to the pressures, so we can solve for the required
time:
In many unsteady-state mass balance problems, it is convenient to take as the system the fluid in some container. Thus, as the
mass of fluid increases or decreases, the volume of the system changes.
Example 3.6. A cylindrical tank 3 m in diameter, with vertical axis, has an inflow line of 0.1-m inside diameter and an outflow
line of 0.2-m inside diameter. Water is flowing in the inflow line at a velocity of 2 m/s and leaving by the outflow line at a
velocity of 1 m/s. Is the level in the tank rising or falling? How fast?
Here we take as our system the instantaneous mass of water in the tank. For this system
The volume of liquid in the tank is decreasing, and the level is falling. The rate of decrease in volume is equal to the cross-
sectional area times the rate of fall in the level:
In the preceding examples, the flowing materials have been uniform single species, e.g., air or water. In most of the rest of this
book we deal with such uniform single species. However, in many problems of great interest two or more components mix inside
the system. If we make the simplest possible mixing assumptionperfect mixing of all componentsthen we can apply the
simple balance equation as before and find useful answers. The perfect mixing assumption is obviously a great simplification of
what must occur in nature, but it is often used because the results are so simple and useful. Two examples illustrate the idea.
The pollutant flow rates are expressed as concentrations (e.g., kilograms per cubic meter) times volumetric flow rates (e.g., cubic
meters per second), so
Equation 3.28 says that the pollutant concentration in the city is equal to that in the air entering the city (the background
concentration) plus a term [qL/(VH)] which indicates how much the pollutant concentration has been increased by the
emissions from the city itself. This is the "box model" or "proportional" or "rollback" equation, which has played a very
important role in the formulation of air pollution regulations in the United States [2].
Example 3.8. Our paint shop will use a special paint that has benzene as a solvent. In the course of an 8-h day, the paint
evaporates 200 kg (4401b) of benzene (q = 200 kg/8 h). The shop dimensions are 10 m x 4 m x 4 m. To protect the health of our
workers, we must limit the concentration of benzene in the shop air to less than or equal to the industrial hygiene standard for
benzene, which is 30 mg/m3. If we wish to keep the concentration c of benzene in the shop at or below this permitted
concentration, how large a flow of ventilating air must we supply?
17/02/2017 Dr. ARKAN JASIM HADI 15
This is very similar to Example 3.7. Here we assume that the benzene is well mixed into the air in the shop and that the air leaving
the shop will have the permitted benzene concentration. Making a steady-state benzene balance on the shop, taking the inlet
airflow as Q, we get
0 = benzene in inlet air + benzene evaporated by the paint benzene in exit air
This example shows that, for the assumption of perfect mixing of benzene into the shop air, it is quite straightforward to
compute the required dilution air to meet the industrial hygiene standard. We also see that this is an impossibly large airflow
rate. If we divide the above flow rate by the cross-sectional area of the shop (4 m x 4 m), we find
This is a very high velocity, which could hardly be used inside a paint shop. Our practical alternatives are to choose a less
toxic solvent, for which the permitted concentration is higher, or to devise some kind of ventilation system, such as a laboratory
fume hood, which will prevent the mixing of the benzene with the air that workers breathe.
The foregoing mass balances were for a small number of flows in and out. Obviously, the same idea can be readily applied to a
much larger number of flows in and out. One equation often used in theoretical fluid mechanics (see Chap. 10) is the mass
balance equation for an arbitrary point in space. We find this equation by defining the coordinates and components of the local
fluid velocity, as shown in Fig. 3.5. Our system is a small open-faced cube.
Writing the analogous terms for faces 3, 4, 5, and 6 and inserting all in Eq. 3.31, we find
By letting , , and approach zero we have shrunk the system to a single point. Thus Eq. 3.36 is the mass balance for
any point in space; it is often called the general continuity equation: Equation 3.37 is the mass balance for any point in space
which contains a constant-density fluid.
All balances can be made from the general balance equation (accumulation = creation - destruction + flow in - flow out) by
dropping the unnecessary terms.
All balances can be divided by time to make rate equations.
In any balance it is necessary to choose and state the boundaries over which the balance is made. Whatever is inside the
boundaries over which the balance is made is called the system. Whatever is outside is called the surroundings