Ce 311b Module 1
Ce 311b Module 1
Module 1
Acceleration of gravity
Universal gas constant Ru = 8.314 kJ kmol · K = 1545 ft · lbf lbmol · °R
Standard atmospheric pressure
Macroscopic Solids hold their shape; no need Liquids take the shape of the Gases expand to fill a closed
Description for a container container and will stay in open container
container
Mobility of Molecules Molecules have low mobility Liquids typically flow easily even Molecules move around freely
because they are bound in a though there are strong intermolecular with little interaction except
structure by strong forces between molecules during collisions; this is why
intermolecular forces gases expand to fill their container
Typical Density Often high; e.g., density of steel Medium; e.g., density of water is Small; e.g., density of air at sea
is 7700 kg m3 1000 kg m3 level is 1.2 kg m3
Molecular Spacing Small—molecules are close Small—molecules are held close Large—on average, molecules are
together together by intermolecular forces far apart
Effect of Normal Stress Produces deformation that may Produces deformation associated with Produces deformation associated
associate with volume change; volume change with volume change
can cause failure
Viscosity NA High; decreases as temperature Low; increases as temperature
increases increases
Compressibility Difficult to compress; bulk Difficult to compress; bulk modulus Easy to compress; bulk modulus
modulus of steel is 160 109 Pa of liquid water is 2.2 109 Pa of a gas at room conditions is
about 1.0 105 Pa
Dimensions
A dimension is a category that represents a physical quantity such as mass, length, time, momentum, force, acceleration, and
energy. To simplify matters, engineers express dimensions using a limited set that are called primary dimensions. Table 1.2
lists one common set of primary dimensions.
Secondary dimensions such as momentum and energy can be related to primary dimensions by using equations. For
example, the secondary dimension “force” is expressed in primary dimensions by using Newton’s second law of motion, F
= ma.
Units
While a dimension expresses a specific type of physical quantity, a unit assigns a number so that the dimension can be
measured. For example, measurement of volume (a dimension) can be expressed using units of liters. Similarly, measurement
of energy (a dimension) can be expressed using units of joules. Most dimensions have multiple units that are used for
measurement. For example, the dimension of “force” can be expressed using units of newtons, pounds-force, or dynes.
Unit Systems
In practice, there are several unit systems in use. The International System of Units (abbreviated SI from the French “Le
Système International d'Unités”) is based on the meter, kilogram, and second.
FLUID PROPERTIES
Mass Density, p
Mass density is defined as the ratio of mass to volume at a point, given by
𝜌 = 𝑚/𝑉
Specific Weight, γ
The gravitational force per unit volume of fluid, or simply the weight per unit volume, is de- fined as specific weight. It is
given the Greek symbol γ (gamma). Water at 20°C has a specific weight of 9790 N m3 (or 62.4 lbf ft3 at 50°F). In contrast,
the specific weight of air at 20°C and standard atmospheric pressure is 11.8 N m3. Specific weight and density are related
by
γ = pg
In practice, engineers need to decide whether or not to model a fluid as constant density or variable density. Usually, a liquid
such as water requires a large change in pressure in order to change the density. Thus, for most applications, liquids can be
considered incompressible and can be assumed to have constant density. An exception to this occurs when different
solutions, such as saline and fresh water, are mixed. A mixture of salt in water changes the density of the water without
changing its volume. Therefore in some flows, such as in estuaries, density variations may occur within the flow field even
though the fluid is essentially incompressible. A fluid wherein density varies spatially is described as nonhomogeneous. This
text emphasizes the flow of homogeneous fluids, so the term incompressible, used throughout the text, implies constant
density.
Specific Gravity, S
The ratio of the specific weight of a given fluid to the specific weight of water at the standard reference temperature 4°C is
defined as specific gravity, S:
γfluid pfluid
S = ------------ = ------------
γwater pwater
The specific weight of water at atmospheric pressure is 9790 N m3. The specific gravity of mercury at 20°C is
133 kN/m3
SHg = ---------------3= 13.6
9.79 kN/m
Because specific gravity is a ratio of specific weights, it is dimensionless and therefore independent of the system of units
used.
Ideal Gas Law
The ideal gas law relates important thermodynamic properties, and is often used to calculate density.
One form of the law is
pV = nRu T
where p is the absolute pressure, V is the volume, n is the number of moles, Ru is the universal gas constant (the same for
all gases), and T is absolute temperature.
Viscosity
The property of viscosity is important to engineering practice because it leads to significant
energy loss when moving fluids contact a solid boundary, or when different zones of fluid are
flowing at different velocities.
Viscosity, µ
Viscosity (also called dynamic viscosity, or absolute viscosity) is a measure of a fluid’s resistance to deformation under shear
stress. For example, crude oil has a higher resistance to shear than does water. Crude oil will pour more slowly than water
from an identical beaker held at the same angle. This relative slowness of the oil implies a low “speed” or rate of strain. The
symbol used to represent viscosity is µ (mu). To understand the physics of viscosity, it is useful to refer back to solid
mechanics and the concepts of shear stress and shear strain. Shear stress, τ, tau, is the ratio of force/area on a surface when
the force is aligned parallel to the area. Shear strain is a change in an interior angle of a cubical element, , that was
originally a right angle. The shear stress on a material element in solid mechanics is proportional to the strain, and the
constant of proportionality is the shear modulus:
shear stress = shear modulus strain
In fluid flow, however, the shear stress on a fluid element is proportional to the rate (speed) of strain, and the constant of
proportionality is the viscosity:
shear stress = viscosity rate of strain
Figure 2.1 depicts an initially rectangular element in a parallel flow field. As the element moves downstream, a shear force
on the top of the element (and a corresponding shear stress in the opposite direction on the bottom of the element) causes
the top surface to move faster (with velocity V + V ) than the bottom (at velocity V). The forward and rearward edges
become inclined at an angle with respect to the vertical. The rate at which changes with time, given by , is the rate
of strain, and can be related to the velocity difference between
Figure 2.1 y
V
Depiction of strain
caused by a shear stress
(force per area) in a
fluid. The rate of strain is
the rate of change of the
interior angle of the
original rectangle.
(V + V ) t
F Vt
V + V
Element at Element at
y
time t time t + t
V
F
Vt
the two surfaces. In time (t) the upper surface moves (V + V)t while the bottom sur-
Kinematic Viscosity, v
Many equations of fluid mechanics include the ratio µ p. Because it occurs so frequently, this ratio has been given the
special name kinematic viscosity. The symbol used to identify ki- nematic viscosity is v (nu). Units of kinematic viscosity v
are m2 s, as shown.
µ N · s m2 2
v = --- ----------------------- = m s
p kg m3
The units for kinematic viscosity in the traditional system are ft2 s.
EXAMPLE 2.2 CALCULATING VISCOSITY OF LIQUID AS A FUNCTION OF TEMPERATURE
The dynamic viscosity of water at 20°C is
1.00 10–3 N · s m2, and the viscosity at 40°C is
6.53 10–4 N · s m2.
Using Equation, estimate the viscosity at 30°C.
Problem Definition
Situation: Viscosity of water is specified at two temperatures.
Find: The viscosity at 30°C by interpolation.
Newtonian fluid
Shear-thickening
dV
dy
stress may not be directly proportional to the rate of strain; these are called non-Newtonian fluids. One class of non-
Newtonian fluids, shear-thinning fluids, has the interesting property that the ratio of shear stress to shear strain decreases as
the shear strain increases (see Fig. 2.2). Some common shear-thinning fluids are toothpaste, catsup, paints, and printer’s ink.
Fluids for which the viscosity increases with shear rate are shear-thickening fluids. Some examples of these fluids are
mixtures of glass particles in water and gypsum-water mixtures. Another type of non-Newtonian fluid, called a Bingham
plastic, acts like a solid for small values of shear stress and then behaves as a fluid at higher shear stress. The shear stress
versus shear strain rate for a Bingham plastic is also shown in Fig. 2.2. This book will focus on the theory and applications
involving Newtonian fluids. For more information on the theory of flow of non-Newtonian fluids, see references (2) and
(3).
dM = p d V + V dp = 0
so
dp dV
V dp = –p dV or ----- = –-------
p V
and the definition of the bulk modulus of elasticity becomes
dp change in pressure
Ev = ------------ = ------------------------------------------------------------------
dp p fractional change in density
The bulk modulus of elasticity of water is approximately 2.2 GN m2, which corresponds to a 0.05% change in volume for a
change of 1 MN m2 in pressure. Obviously, the term incompressible is justifiably applied to water because it has such a small
change in volume for a very large change in pressure.
The elasticity of an ideal gas is proportional to the pressure, according to the ideal gas law. For an isothermal (constant-
temperature) process,
dp
- -- = RT
dp
so
dp
Ev = p---- = pRT = p
dp
For an adiabatic process, Ev = kp, where k is the ratio of specific heats, cp cv .
The elasticity or compressibility of a gas is important in high-speed gas flows where pressure variations can cause significant density
changes.
Surface Tension
Surface tension, σ (sigma), is a material property whereby a liquid at a material interface, usu-
d ally liquid-gas, exerts a force per unit length along the surface. According to the theory of mo-
Surface-tension lecular attraction, molecules of liquid considerably below the surface act on each other by forces
force that are equal in all directions. However, molecules near the surface have a greater attraction for
each other than they do for molecules below the surface because of the presence of a different
h z substance above the surface. This produces a layer of surface molecules on the liquid that acts
like a stretched membrane. Because of this membrane effect, each portion of the liquid surface
exerts “tension” on adjacent portions of the surface or on objects that are in contact with the liq-
uid surface. This tension acts in the plane of the surface, and is given by:
Fσ = σL
Figure 2.3 where L is the length over which the surface tension acts.
Capillary action
Surface tension for a water–air surface is 0.073 N m at room temperature. The magnitude of
in a small tube.
surface tension decreases with increasing temperature; tabulated values for different liquids
as a function of temperature are available in the literature and online. The effect of surface
tension is illustrated for the case of capillary action (rise above a static water level at
atmospheric pressure) in a small tube (Fig. 2.3). Here the end of a small-diameter tube is
inserted into a reservoir of water, and the characteristic curved water surface profile occurs within the tube. The
relatively greater attraction of the water molecules for the glass rather than the air causes the water surface to curve
upward in the region of the glass wall. Then the surface tension force acts around the circumference of the tube, in
the direction indicated. It may be assumed that the contact angle θ (theta) is equal to 0° for water against glass. The
surface tension force produces a net upward force on the water that causes the water in the tube to rise above the water
surface in the reservoir.
Other manifestations of surface tension include the excess pressure (over and above atmospheric pressure) created
inside droplets and bubbles because there is necessarily a pressure difference across a curved interface; the breakup
of a liquid jet into droplets; the shape and motion of bubbles, the structure of foams, and the binding together of
wetted granular material, such as soil.
Surface tension forces for several different cases are shown in Fig. 2.8. Case (a) is a spherical droplet of radius r.
The surface tension force is balanced by the internal pressure.
A-
3 Fσ = σL = pA
o
r 2πrσ
= pπr2
2σ
p=
-
r
Case (b) is a bubble of radius r that has internal and external surfaces and the
surface- tension force acts on both surfaces, so
p = 2 σ-
r
Case (c) is a cylinder supported by surface-tension forces. The liquid does not
wet the cylinder surface. The maximum weight the surface tension can support is
W = 2Fσ = 2σL
where L is the length of the cylinder.
Problem Definition
Situation: A glass tube of small diameter placed in an open Because the contact angle θ for water against glass is so
reservoir of water induces capillary rise. small, it can be assumed to be 0°; therefore
Find: The height the water will rise above the reservoir level. cosθ 1. Therefore:
Sketch: See Figure 2.3.
4
2. Solve for h :
Plan ----σ- ---------------4-------0--.--0--7--3----N-------m
h 4 ---------- 18.6 mm
Perform a force balance on water that has risen in the tube. 9790 N m3 1.6 10–3 m
Solve for h.
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Vapor Pressure
The pressure at which a liquid will vaporize, or boil, at a given temperature, is called its vapor pressure. This means that
boiling occurs whenever the local pressure equals the vapor pressure. Vapor pressure increases with temperature. Note
that there are two ways to boil a liquid. One way is to raise the temperature, assuming that the pressure is fixed. For
water at
14.7 psia, this can be accomplished by increasing the temperature of water at sea level to 212°F, thus reaching the
temperature where the vapor pressure is equal to the same value. However, boiling can also occur in water at
temperatures much below 212°F if the pressure in the water is reduced to the vapor pressure of water corresponding to
that lower temperature. For example, the vapor pressure of water at 50°F (10°C) is 0.178 psia (approximately 1% of
standard atmospheric pressure). Therefore, if the pressure in water at 50°F is reduced to 0.178 psia, the water boils.*
Such boiling often occurs in localized low-pressure zones of flowing liquids, such as on the suction side of a pump.
When localized low-pressure boiling does occur in flowing liquids, vapor bubbles start growing in local regions of very
low pressure and then collapse in regions of higher pressure downstream.
PROBLEMS:
1. An engineer living at an elevation of 2500 ft is conducting experiments to verify predictions of glider performance. To
process data, density of ambient air is needed. The engineer measures temperature (74.3°F) and atmospheric pressure
(27.3 inches of mercury). Calculate density in units of kg m3. Compare the calculated value with data from Table A.3
and make a recommendation about the effects of elevation on density; that is, are the effects of elevation significant?
2. Determine the density and specific weight of methane gas at a pressure of 300 kN m2 absolute and 60°C.
3. A 10 m3 oxygen tank is at 15°C and 800 kPa. The valve is opened, and some oxygen is released until the pressure in the tank
drops to 600 kPa. Calculate the mass of oxygen that has been released from the tank if the temperature in the tank does not
change during the process.
4. What is the change in the viscosity and density of water be- tween 10°C and 70°C? What is the change in the viscosity and
density of air between 10°C and 70°C? Assume standard atmospheric pressure (p = 101 kN m2 absolute).
5. Find the kinematic and dynamic viscosities of air and water at a temperature of 40°C (104°F) and an absolute pressure of 170
kPa (25 psia).
6. The velocity distribution for water (20°C) near a wall is given by u = a(y b)1/6, where a = 10 m s, b = 2 mm, and
y is the distance from the wall in mm. Determine the shear stress in the water at y = 1 mm.
u
y
x
7. Calculate the pressure increase that must be applied to water to reduce its volume by 2%.
8. A spherical soap bubble has an inside radius R, a film thickness t, and a surface tension σ. Derive a formula for the pressure
within the bubble relative to the outside atmospheric
9. A water column in a glass tube is used to measure the pressure in a pipe. The tube is 1 4 in. (6.35 mm) in diameter. How much
of the water column is due to surface-tension effects? What would be the surface-tension effects if the tube were 1 8 in. (3.2 mm)
or 1 32 in. (0.8 mm) in diameter?
10. What is the pressure within a 1 mm spherical droplet of water relative to the atmospheric pressure outside?
11. Water is at 20°C, and the pressure is lowered until bubbles are noticed to be forming. What must the magnitude of the
pressure be?
12. The vapor pressure of water at 100°C is 101 kN m2, because water boils under these conditions. The vapor pressure of
water decreases approximately linearly with decreasing temperature at a rate of 3.1 kN m2 C. Calculate the boiling
temperature of water at an altitude of 3000 m, where the atmospheric pressure is 69 kN m2 absolute.
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5
Table A.1 COMPRESSIBLE FLOW TABLES FOR AN IDEAL GAS WITH k = 1.4
M or M1 = local number or Mach number upstream of a normal shock wave; p pt = ratio of static
pressure to total pressure; p pt = ratio of static density to total density; T Tt = ratio of static
temperature to total temperature; A A* = ratio of local cross-sectional area of an isentropic stream
tube to cross-sectional area at the point where M = 1; M2 = Mach number downstream of a normal
shock wave; p2 p1 = static pressure ratio across a normal shock wave; T2 T1 = static pressure ratio
across a normal shock wave; pt2 pt 1 = total pressure ratio across normal shock wave.
Subsonic Flow
M p pt p pt T Tt A A*
0.00 1.0000 1.0000 1.0000
0.05 0.9983 0.9988 0.9995 11.5914
0.10 0.9930 0.9950 0.9980 5.8218
0.15 0.9844 0.9888 0.9955 3.9103
0.20 0.9725 0.9803 0.9921 2.9630
0.25 0.9575 0.9694 0.9877 2.4027
0.30 0.9395 0.9564 0.9823 2.0351
0.35 0.9188 0.9413 0.9761 1.7780
0.40 0.8956 0.9243 0.9690 1.5901
0.45 0.8703 0.9055 0.9611 1.4487
0.50 0.8430 0.8852 0.9524 1.3398
0.52 0.8317 0.8766 0.9487 1.3034
0.54 0.8201 0.8679 0.9449 1.2703
0.56 0.8082 0.8589 0.9410 1.2403
0.58 0.7962 0.8498 0.9370 1.2130
0.60 0.7840 0.8405 0.9328 1.1882
0.62 0.7716 0.8310 0.9286 1.1657
0.64 0.7591 0.8213 0.9243 1.1452
0.66 0.7465 0.8115 0.9199 1.1265
0.68 0.7338 0.8016 0.9153 1.1097
0.70 0.7209 0.7916 0.9107 1.0944
0.72 0.7080 0.7814 0.9061 1.0806
0.74 0.6951 0.7712 0.9013 1.0681
0.76 0.6821 0.7609 0.8964 1.0570
0.78 0.6691 0.7505 0.8915 1.0471
0.80 0.6560 0.7400 0.8865 1.0382
0.82 0.6430 0.7295 0.8815 1.0305
0.84 0.6300 0.7189 0.8763 1.0237
0.86 0.6170 0.7083 0.8711 1.0179
0.88 0.6041 0.6977 0.8659 1.0129
0.90 0.5913 0.6870 0.8606 1.0089
0.92 0.5785 0.6764 0.8552 1.0056
0.94 0.5658 0.6658 0.8498 1.0031
0.96 0.5532 0.6551 0.8444 1.0014
0.98 0.5407 0.6445 0.8389 1.0003
1.00 0.5283 0.6339 0.8333 1.0000
(Continued)
A-
6
Table A.1 COMPRESSIBLE FLOW TABLES FOR AN IDEAL GAS WITH k = 1.4 (Continued)
Supersonic Flow Normal Shock Wave
M1 p pt p pt T Tt A A* M2 p2 p1 T2 T1 pt 2 pt 1
1.00 0.5283 0.6339 0.8333 1.000 1.0000 1.000 1.000 1.0000
1.01 0.5221 0.6287 0.8306 1.000 0.9901 1.023 1.007 0.9999
1.02 0.5160 0.6234 0.8278 1.000 0.9805 1.047 1.013 0.9999
1.03 0.5099 0.6181 0.8250 1.001 0.9712 1.071 1.020 0.9999
1.04 0.5039 0.6129 0.8222 1.001 0.9620 1.095 1.026 0.9999
1.05 0.4979 0.6077 0.8193 1.002 0.9531 1.120 1.033 0.9998
1.06 0.4919 0.6024 0.8165 1.003 0.9444 1.144 1.039 0.9997
1.07 0.4860 0.5972 0.8137 1.004 0.9360 1.169 1.046 0.9996
1.08 0.4800 0.5920 0.8108 1.005 0.9277 1.194 1.052 0.9994
1.09 0.4742 0.5869 0.8080 1.006 0.9196 1.219 1.059 0.9992
1.10 0.4684 0.5817 0.8052 1.008 0.9118 1.245 1.065 0.9989
1.11 0.4626 0.5766 0.8023 1.010 0.9041 1.271 1.071 0.9986
1.12 0.4568 0.5714 0.7994 1.011 0.8966 1.297 1.078 0.9982
1.13 0.4511 0.5663 0.7966 1.013 0.8892 1.323 1.084 0.9978
1.14 0.4455 0.5612 0.7937 1.015 0.8820 1.350 1.090 0.9973
1.15 0.4398 0.5562 0.7908 1.017 0.8750 1.376 1.097 0.9967
1.16 0.4343 0.5511 0.7879 1.020 0.8682 1.403 1.103 0.9961
1.17 0.4287 0.5461 0.7851 1.022 0.8615 1.430 1.109 0.9953
1.18 0.4232 0.5411 0.7822 1.025 0.8549 1.458 1.115 0.9946
1.19 0.4178 0.5361 0.7793 1.026 0.8485 1.485 1.122 0.9937
1.20 0.4124 0.5311 0.7764 1.030 0.8422 1.513 1.128 0.9928
1.21 0.4070 0.5262 0.7735 1.033 0.8360 1.541 1.134 0.9918
1.22 0.4017 0.5213 0.7706 1.037 0.8300 1.570 1.141 0.9907
1.23 0.3964 0.5164 0.7677 1.040 0.8241 1.598 1.147 0.9896
1.24 0.3912 0.5115 0.7648 1.043 0.8183 1.627 1.153 0.9884
1.25 0.3861 0.5067 0.7619 1.047 0.8126 1.656 1.159 0.9871
1.30 0.3609 0.4829 0.7474 1.066 0.7860 1.805 1.191 0.9794
1.35 0.3370 0.4598 0.7329 1.089 0.7618 1.960 1.223 0.9697
1.40 0.3142 0.4374 0.7184 1.115 0.7397 2.120 1.255 0.9582
1.45 0.2927 0.4158 0.7040 1.144 0.7196 2.286 1.287 0.9448
1.50 0.2724 0.3950 0.6897 1.176 0.7011 2.458 1.320 0.9278
1.55 0.2533 0.3750 0.6754 1.212 0.6841 2.636 1.354 0.9132
1.60 0.2353 0.3557 0.6614 1.250 0.6684 2.820 1.388 0.8952
1.65 0.2184 0.3373 0.6475 1.292 0.6540 3.010 1.423 0.8760
1.70 0.2026 0.3197 0.6337 1.338 0.6405 3.205 1.458 0.8557
1.75 0.1878 0.3029 0.6202 1.386 0.6281 3.406 1.495 0.8346
1.80 0.1740 0.2868 0.6068 1.439 0.6165 3.613 1.532 0.8127
1.85 0.1612 0.2715 0.5936 1.495 0.6057 3.826 1.569 0.7902
1.90 0.1492 0.2570 0.5807 1.555 0.5956 4.045 1.608 0.7674
1.95 0.1381 0.2432 0.5680 1.619 0.5862 4.270 1.647 0.7442
2.00 0.1278 0.2300 0.5556 1.688 0.5774 4.500 1.688 0.7209
2.10 0.1094 0.2058 0.5313 1.837 0.5613 4.978 1.770 0.6742
2.20 0.9352–1† 0.1841 0.5081 2.005 0.5471 5.480 1.857 0.6281
2.30 0.7997–1 0.1646 0.4859 2.193 0.5344 6.005 1.947 0.5833
2.50 0.5853–1 0.1317 0.4444 2.637 0.5130 7.125 2.138 0.4990
2.60 0.5012–1 0.1179 0.4252 2.896 0.5039 7.720 2.238 0.4601
2.70 0.4295–1 0.1056 0.4068 3.183 0.4956 8.338 2.343 0.4236
2.80 0.3685–1 0.9463–1 0.3894 3.500 0.4882 8.980 2.451 0.3895
2.90 0.3165–1 0.8489–1 0.3729 3.850 0.4814 9.645 2.563 0.3577
3.00 0.2722–1 0.7623–1 0.3571 4.235 0.4752 10.330 2.679 0.3283
3.50 0.1311–1 0.4523–1 0.2899 6.790 0.4512 14.130 3.315 0.2129
4.00 0.6586–2 0.2766–1 0.2381 10.72 0.4350 18.500 4.047 0.1388
(Continued)
A-
7
Table A.1 COMPRESSIBLE FLOW TABLES FOR AN IDEAL GAS WITH k = 1.4 (Continued)
Supersonic Flow Normal Shock Wave
M1 p pt p pt T Tt A A* M2 p2 p1 T2 T1 pt 2 pt 1
4.50 0.3455–2 0.1745–1 0.1980 16.56 0.4236 23.460 4.875 0.9170–1
5.00 0.1890–2 0.1134–1 0.1667 25.00 0.4152 29.000 5.800 0.6172–1
5.50 0.1075–2 0.7578–2 0.1418 36.87 0.4090 35.130 6.822 0.4236–1
6.00 0.6334–2 0.5194–2 0.1220 53.18 0.4042 41.830 7.941 0.2965–1
6.50 0.3855–2 0.3643–2 0.1058 75.13 0.4004 49.130 9.156 0.2115–1
7.00 0.2416–3 0.2609–2 0.9259–1 104.1 0.3974 57.000 10.47 0.1535–1
7.50 0.1554–3 0.1904–2 0.8163–1 141.8 0.3949 65.460 11.88 0.1133–1
8.00 0.1024–3 0.1414–2 0.7246–1 190.1 0.3929 74.500 13.39 0.8488–2
8.50 0.6898–4 0.1066–2 0.6472–1 251.1 0.3912 84.130 14.99 0.6449–2
9.00 0.4739–4 0.8150–3 0.5814–1 327.2 0.3898 94.330 16.69 0.4964–2
9.50 0.3314–4 0.6313–3 0.5249–1 421.1 0.3886 105.100 18.49 0.3866–2
10.00 0.2356–4 0.4948–3 0.4762–1 535.9 0.3876 116.500 20.39 0.3045–2
SOURCE: V. L.Streeter (ed.), Handbook of Fluid Dynamics, McGraw-Hill Book Company, New York, 1961; also R. E. Bolz and G. L. Tuve, Handbook of Tables
for Applied Engineering Science, CRC Press, Inc. Cleveland, 1973; and Handbook of Chemistry and Physics, Chemical Rubber Company, 1951.
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kg m3 N m3 N · s m2 m2 s
SOURCE: Reprinted with permission from R. E. Bolz and G. L. Tuve, Handbook of Tables for Applied Engineering Science, CRC
Press, Inc., Cleveland, 1973. Copyright © 1973 by The Chemical Rubber Co., CRC Press, Inc.
A-
9
kg m3 N m3 N · s m2 m2 s N m*
Liquid and Specific
Temperature (slugs ft3) Gravity (lbf ft3) (lbf-s ft2) (ft2 s) (lbf ft)
Ethyl alcohol(1)(3) 799 0.79 7,850 1.2 10–3 1.5 10–6 2.2 10–2
20°C (68°F) (1.55) (50.0) (2.5 10–5) (1.6 10–5) (1.5 10–3)
Carbon tetrachloride(3) 1,590 1.59 15,600 9.6 10–4 6.0 10–7 2.6 10–2
20°C (68°F) (3.09) (99.5) (2.0 10–5) (6.5 10–6) (1.8 10–3)
20°C (68°F) (2.45) (78.5) (2.95 10–2) (1.22 10–2) (4.3 10–3)
Kerosene(1)(2) 814 0.81 8,010 1.9 10–3 2.37 10–6 2.9 10–2
20°C (68°F) (1.58) (51) (4.0 10–5) (2.55 10–5) (2.0 10–3)
Mercury(1)(3) 13,550 13.55 133,000 1.5 10–3 1.2 10–7 4.8 10–1
20°C (68°F) (26.3) (847) (3.1 10–5) (1.3 10–6) (3.3 10–2)
Sea water 10°C 1,026 1.03 10,070 1.4 10–3 1.4 10–6
at 3.3% salinity (1.99) (64.1) (2.9 10–5) (1.5 10–5)
Oils—38°C (100°F) 870 0.87 8,530 3.6 10–2 4.1 10–5
SAE 10W(4) (1.69) (54.4) (7.5 10–4) (4.4 10–4)
SAE 10W-30(4) 880 0.88 8,630 6.7 10–2 7.6 10–5
(1.71) (55.1) (1.4 10–3) (8.2 10–4)
SAE 30(4) 880 0.88 8,630 1.0 10–1 1.1 10–4
(1.71) (55.1) (2.1 10–3) (1.2 10–3)