Apendice Afox
Apendice Afox
785
786 Appendix A Fluid Property Data
1.000
0.990
0.970
0.960
For water at 4⬚C, ρ = 1000 kg/m3
0.950
–20 0 20 40 60 80 100 120
Temperature, ⬚C
(a) Water
13.60
(referred to water at 4⬚C)
Specific gravity, SG
13.50
13.40
13.30
–20 0 20 40 60 80 100 120
Temperature, ⬚C
(b) Mercury
Fig. A.1 Specific gravity of water and mercury as functions of temperature. (Data from Refer-
ence [1].) (The specific gravity of mercury varies linearly with temperature. The variation is given
by SG 5 13.60 2 0.00240 T when T is measured in degrees C.)
Table A.1
Specific Gravities of Selected Engineering Materials
(a) Common Manometer Liquids at 20 C
Table A.1
Specific Gravities of Selected Engineering Materials (continued)
(b) Common Materials
Aluminum 2.64
Balsa wood 0.14
Brass 8.55
Cast Iron 7.08
Concrete (cured) 2.4a
Concrete (liquid) 2.5a
Copper 8.91
Ice (0 C) 0.917
Lead 11.4
Oak 0.77
Steel 7.83
Styrofoam (1 pcfb) 0.0160
Styrofoam (3 pcf) 0.0481
Uranium (depleted) 18.7
White pine 0.43
Table A.2
Physical Properties of Common Liquids at 20 C
Liquid Isentropic Bulk Modulusa (GN/m2) Specific Gravity (—)
Table A.3
Properties of the U.S. Standard Atmosphere
Geometric Altitude (m) Temperature (K) p/pSL (—) ρ/ρSL(—)
Table A.4
Surface Tension of Common Liquids at 20 C
Surface Tension,
Liquid σ (mN/m)a Contact Angle, θ (degrees)
Air
(a) In contact with air Liquid
θ
Benzene 28.9
Carbon tetrachloride 27.0
Ethanol 22.3
Glycerin 63.0
Hexane 18.4
Kerosene 26.8
Lube oil 2535
Mercury 484 140
Methanol 22.6
Octane 21.8
Water 72.8 B0
Water
(b) In contact with water
Liquid
θ
Benzene 35.0
Carbon tetrachloride 45.0
Hexane 51.1
Mercury 375 140
Methanol 22.7
Octane 50.8
Source: Data from References [1, 5, 8, 9].
a
1 mN/m 5 1023 N/m.
(Compare this with y 5 mx 1 c.) From a plot of T 3/2/μ versus T, one obtains the
slope, 1/b, and the intercept, S/b. For air,
kg
b 5 1:458 3 1026
msK1=2
S 5 110:4 K
These constants were used with Eq. A.1 to compute viscosities for the standard
atmosphere in [7], the air viscosity values at various temperatures shown in
Table A.10, and using appropriate conversion factors, the values shown in Table A.9.
b. Liquids
Viscosities for liquids cannot be estimated well theoretically. The phenomenon of
momentum transfer by molecular collisions is overshadowed in liquids by the effects
of interacting force fields among the closely packed liquid molecules.
Liquid viscosities are affected drastically by temperature. This dependence on
absolute temperature may be represented by the empirical equation
μ 5 AeB=ðT2CÞ ðA:2Þ
or the equivalent form
μ 5 A10B=ðT2CÞ ðA:3Þ
1.0 Glycerin
8
6
4 Castor oil
2
SAE 30 oil
–1
1⫻10
8
6 SAE 10W-30 oil
4
Absolute viscosity, μ (N · s/m2)
2
SAE 10W oil
1⫻10–2
8
6
2
Mercury
Octane
1⫻10–3
8 Kerosene
6
Water
Carbon
tetrach
4 loride
Heptane
1⫻10–4
8
6
4
Methane Carbon dioxide
Helium
2
Air
1⫻10–5
8 Hydrogen
6
–20 0 20 40 60 80 100 120
Temperature, T (⬚C)
Fig. A.2 Dynamic (absolute) viscosity of common fluids as a function of
temperature. (Data from References [1, 6, and 10].)
The graphs for air and water were computed from the Excel workbook Absolute
Viscosities, using Eq. A.1 and Eq. A.3, respectively. The workbook can be used
to compute viscosities of other fluids if constants b and S (for a gas) or A, B, and
C (for a liquid) are known.
the water viscosity values at various temperatures shown in Table A.8, and using
appropriate conversion factors, the values shown in Table A.7.
Note that the viscosity of a liquid decreases with temperature, while that of a gas
increases with temperature.
1⫻10–2
8
6
1 m2/s = 10.8 ft2/s
4
SA
E
30
1⫻10–3
oil
8 SA
Gl
yc
6 E
er
10
in
W
4 -3
0
oi
l
2
Helium
Kinematic viscosity, ν (m2/s)
Hydrogen
1⫻10–4
8
SA
6 E
10
4 W
oi
l Methane
2 Air
1⫻10–5
8
ioxide
6 Carbon d
4
Kero
2 sene
Wa
ter
–6
1⫻10
8
6 Heptane
Octane
4
Carbon te
trachloride
2
Mercury
–7
1⫻10
8
6
–20 0 20 40 60 80 100 120
Temperature, T (⬚C)
Fig. A.3 Kinematic viscosity of common fluids (at atmospheric pressure) as a function of temperature. (Data
from References [1, 6, and 10].)
b. Liquids
The viscosities of most liquids are not affected by moderate pressures, but large
increases have been found at very high pressures. For example, the viscosity of water
at 10,000 atm is twice that at 1 atm. More complex compounds show a viscosity
increase of several orders of magnitude over the same pressure range.
More information may be found in Reid and Sherwood [11].
A.5 Properties of Common Gases, Air and Water 793
Table A.5
Allowable Viscosity Ranges for Lubricants
Table A.6
Thermodynamic Properties of Common Gases at STPa
Rb cp cv cp Rb cp cv
k5
J J J cv ftlbf Btu Btu
Chemical Molecular kgK kgK kgK lbm R lbm R lbm R
ðÞ
Gas Symbol Mass, Mm
Table A.7
Properties of Water (U.S. Customary Units)
Dynamic Kinematic Surface Vapor Bulk
Temperature, Density, Viscosity, Viscosity, Tension, Pressure, Modulus,
T ( F) ρ (slug/ft3) μ (lbfs/ft2) ν (ft2/s) σ (lbf/ft) pv (psia) Ev (psi)
Table A.8
Properties of Water (SI Units)
Dynamic Kinematic Surface Vapor Bulk
Temperature, Density, Viscosity, Viscosity, Tension, Pressure, Modulus,
T ( C) ρ (kg/m3) μ (N s/m2) ν (m2/s) σ (N/m) pv (kPa) Ev (GPa)
Table A.9
Properties of Air at Atmospheric Pressure (U.S. Customary Units)
Dynamic Kinematic
Temperature, Density, Viscosity, Viscosity,
T ( F) ρ (slug/ft3) μ (lbf s/ft2) ν (ft2/s)
Table A.10
Properties of Air at Atmospheric Pressure (SI Units)
Dynamic Kinematic
Temperature, Density, Viscosity, Viscosity,
T ( C) ρ (kg/m3) μ (N s/m2) ν (m2/s)