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V 1.0
III. Parameters 5
Appendix G: References 32
Symbol Definition
Cd Coefficient of discharge
Cp Specific heat at constant pressure
d Throat diameter at flowing temperature
davg Throat diameter at average temperature
dr Throat diameter at reference temperature
D Pipe diameter at flowing temperature
Davg Pipe diameter at average temperature
Dc Derivative of the correlation value of C d
Dr Pipe diameter at reference temperature
Ev Velocity of approach factor
Fc Correlation value of C d
Gi Ideal gas relative density
k Isentropic exponent
L1 Upstream tap position
L2 Downstream tap position
Mrair Molecular weight of air
Mw Molecular weight
Pc Critical pressure
Pf Flowing pressure
Qm Mass flow rate
R Universal gas constant
Re Reynolds number
Tavg Average temperature/Median value of specified temperature range
Tc Critical temperature
Tf Flowing temperature
Tr Reference temperature
v Specific volume
x Ratio of differential pressure to flowing pressure
Y Fluid expansion factor
Zf Compressibility at flowing conditions
α1 Linear coefficient of thermal expansion of primary element
α2 Linear coefficient of thermal expansion of pipe
β Ratio of throat diameter to pipe diameter
∆P Differential pressure
µf Absolute viscosity of flowing fluid
ρf Density of fluid at flowing temperature
Specify Pipe/Throat:
- Diameters at reference temperature
- Materials
π 2
Qm Ev Cd d Y 2ρ f ∆ P
4
Cd = coefficient of discharge
d = throat diameter at flowing temperature
Ev = velocity of approach factor
Qm = mass flow rate
Y = fluid expansion factor
∆P = differential pressure
ρ f = density of fluid at flowing temperature
d dr 1 α 1 Tf Tr D Dr 1 α 2 Tf Tr
d avg
β
Davg
1
Ev
4
1 β
k = isentropic exponent
Pf = flowing pressure
∆P = differential pressure
Y = fluid expansion factor
k.( 1
k 4 k
x) 1 β 1 (1 x)
Y
k 1 2 x
4 k
1 β (1 x)
x = ∆P/ P f
For Gas:
Cp
k
Cp R
2 2
C E
Tavg Tavg
Cp A B D
C E
sinh cosh
Tavg Tavg
Cp = specific heat at constant pressure
R = universal gas constant
A, B, C, D, and E are constants provided by AIChE/DIPPR database
For Liquid:
Y = 1 therefore determination of k is not necessary
For Steam:
k is estimated using the following linear approximation:
k 1.33544 6.24543 . 10 5
Tavg
For Gas:
Pf M w
ρf
Zf R Tf
Mw = molecular weight
Zf = compressibility at flowing conditions
2.5
2
Tc Tc
a .42748 R b .08664 R
Pc Pc
3
R . Tf 2 a 2
b . R . Tf a .b
v v b v =0
Pf Pf . Tf Pf Pf . Tf
.5 .5
Pc = critical pressure
Tc = critical temperature
v = specific volume
For Liquid:
A
ρf
D
T
f
1 1
C
B
For Steam:
ρf is calculated from Tables S-1 through S-5 from the ASME International Steam
Tables. Density is equal to the inverse of specific volume (v).
Zf is calculated using the natural gas compressibility equations from AGA Report 8.
These equations are contained in Appendix D.
For Gas:
B
A Tf
µf
C D
1
Tf Tf
2
For Liquid:
B E
A Cln T D T
T f f
f
µf e
For Steam:
µ f is estimated using the following linear approximation:
6
µ 7.51661 0.02249 Tf 10
f
***For these primary elements, C d is a function of Reynolds number, and Reynolds num-
ber is a function of the unknown mass flow. Therefore, C d can not be directly calculated
and it is necessary to guess values for C d and Reynolds number and use an iterative
process to find the exact values. A detailed description of this iterative process is con-
tained in Appendix D.
Assume an initial value of 4000 for the Reynolds number to get the following equations:
4 1.3
8.5 L 6L β L2 L2
.0712 . e .1145 . e
2 8 1 1 1.1
Cd0 .5961 .0291 β .229 β .0433 .0232 .014853 β
1 β
4 1 β 1 β
0.7
Cd1 .0244 β
4
Cd2 .145 β
4.8
Cd3 .1177 β
4.8 1.3
8.5 L 6L β .0113 L2 L2
.057 . e .0916 . e 7.232 . 10
1 1 3 1.9
Cd4 .0346 β
1 β
4 1 β 1 β
Calculate for X:
4000 Dµ
X
Cd0 . Ev Yd . 2 ρ f . ∆ P
2
Recalculate X with new value of C d(1) in place of C d. Use this value of X to recal-
culate F c , D c, and δCd. Continue repeating this process until δCd < 5x10-6 .
6 1.15
4.1 2 4.15 10
Cd 0.9900 0.2262 β 0.00175 β 0.0033 β
Re
6 0.5
.5 10
Cd 0.9975 0.00653 . β .
Re
Cd = 0.984 D
Cd = 0.984 D
Cd = 0.995
D
Cd = 0.995
D
Cd = 0.985 D
4
4 12 4 4 . 1 β
Cd 0.598 0.468 β 10 β 1 β 0.87 8.1 β
Re
Gas Database
Fluid Mw Pc Tc Cp Viscosity
A B C D E A B C D
Acetic Acid
Acetone
Acetonitrile
Acetylene
Acrylonitrile
Liquid Database
A B C D A B C D E
Acetic Acid
Acetone
Acetonitrile
Acetylene
Acrylonitrile
It can be assumed that the isentropic exponent does not vary with changing
pressure, therefore it is only a function of temperature. To determine an equation for
isentropic exponent as a function of temperature, various values of temperature were
inputted into the software. The corresponding values of isentropic exponent were then
graphed and a trend line was formulated. The equation of this trend line would provide
values of isentropic exponent for all possible values of temperature.
The following table is the values of isentropic exponent provided by the software
at various temperatures:
1.34
1.33
1.32
1.31
Isentropic Exponent (k)
1.3
1.29
1.28
1.27
1.26
k = -6.24543E-05T + 1.33544
1.25
1.24
1.23
0 200 400 600 800 1000 1200 1400 1600
Temperature (F)
According to the ASME Steam Tables, steam viscosity is a function of both tem-
perature and pressure. Its value can be found by applying temperature and pressure
to Table 8 of the ASME Steam Tables. Various software was also analyzed to deter-
mine what assumptions could be made.
After studying Table 8, it can be assumed that viscosity does not vary with
changing pressure. To determine an equation for viscosity as strictly a function of tem-
perature, various values of temperature were inputted into the software, while main-
taining a constant pressure. The corresponding values for viscosity were then graphed
and a trend line was formulated. The equation of this trend line would provide values
for viscosity for all possible values of temperature.
The following table is the values of steam viscosity provided by the software at
various temperatures and constant pressure:
Steam Viscosity
30
25
20
Viscosity (10^-6 lb/ft-s)
-6
Viscosity = (0.01511T + 5.05093)*10
15
10
0
0 200 400 600 800 1000 1200 1400 1600
Temperature (F)
If a liquid is used that is not listed in the database, then the following information
must be provided in order to complete the necessary calculations:
The following method for solving liquid viscosity is derived from Figure 2.19 of the
Flow Measurement Engineering Handbook:
Solve for Y:
Y log µ 1 1
Solve for T:
15 6 12 5 11 4 7 3 4 2 2
4.4 x10 T 3.84 x10 T 3.37 x10 T 9.23 x10 T 3.66 x10 T 6.46 x10 T 6 Y 0
Calculate T1:
T1 = T + Tf - T1
Solve for Y1 :
1 15 1 6 12 1 5 11 1 4 7 1 3 4 1 2 2 1
Y 4.4 x10 T 3.84 x10 T 3.37 x10 T 9.23 x10 T 3.66 x10 T 6.46 x10 T 6
1 1
µf log Y 1
If a gas is used that is not listed in the database, then the following information
must be provided in order to complete the necessary calculations:
Use the provided isentropic exponent along with the equations from Section VI
to solve for the expansion factor. Use provided molecular weight and compressibility
along with the gas equation from Section VIII to solve for the gas density. Use the fol-
lowing equation to solve for the gas viscosity:
1.5
Tf T1 0.9 Tc
µf µ1
T1 Tf 0.9 Tc
There are three methods that can be used to solve for the compressibility factor
of natural gas. The detail characterization method requires that the mole fraction of all
elements of the natural gas be known. The gross characterization method has two op-
tions. One option requires that the real gas relative density, volumetric gross heating
value, and the mole fraction of carbon dioxide must be known; while the other option
requires that the real gas relative density, mole fraction of carbon dioxide, and mole
fraction of nitrogen must be known. Once a method is chosen use the corresponding
equations to solve for the compressibility of natural gas:
2
N 5 N 1 N 5
5 2 5 2
K = xi Ki 2 xi xj Kij 1 Ki Kj
i= 1 i= 1 j= i 1
18 N N 3
u u
n. n 2
B an T xi xj Eij Ki Kj B'nij
n=1 i= 1 j= 1
an = constant given in Table 4
Eij = second virial coefficient binary energy parameter
B`nij = binary characterization coefficient
1
2
Eij E'ij Ei Ej
Ei = characteristic energy parameter for ith component (Table 5)
E`ij = second virial coefficient energy binary interaction parameter (Table 6)
N N 1 N
G xi Gi xi xj G'ij 1 Gi Gj
i= 1 i= 1 j= i 1
N
Q xi Qi
i= 1
N
2
F xi Fi
i= 1
2
N 5 N 1 N 5
2 5 2
U xi Ei 2 xi xj Uij 1 Ei Ej
i= 1 i= 1 j= i 1
Uij = binary interaction parameter for conformal energy (Table 6)
3
D K d
d = molar density (moles per unit volume)
Solve for d using following equation:
18 58 k
n
u u k c D
n n n b n
P dRT 1 Bd D C'n T C'n T bn cn kn D D e
n = 13 n = 13
Z = compressibility factor
Bmix = second virial coefficient for the mixture
Cmix = third virial coefficient for the mixture
d = molar density (moles per unit volume)
N N
Bmix Bij xi xj
i= 1 j= 1
Bij = individual component interaction second virial coefficient
N = number of components in gas mixture
xi , xj , xk = mole fractions of gas components
N N N
Cmix Cijk xi xj xk
i= 1 j= 1 k= 1
Cijk = individual component interaction third virial coefficient
2
Bij b0 b1 T b2 T
b0, b1, b2 = constants given in Table 7
T = temperature
2
Cijk c0 ci T c2 T
c 0, c1, c2 = constants given in Table 7
2
BCH CH
B0 B1 HCH B2 HCH
2
CCH CH CH
C0 C1 HCH C2 HCH
2
Bi b i0 b i1 T b i2 T
2
Ci ci0 ci1 T ci2 T
i = 0, 1, 2
bi0 , bi1 , bi2 , ci0 , c i1 , ci2 = constants given in Table 8
1
2
BCO2 CH
0.865 BCO2 CO2
BCH CH
1
3
2
CN2 CH CH
( 0.92 0.0013 ( T 270 ) ) CCH CH CH
CN2 N2 N2
1
3
2
CN2 N2 CH
( 0.92 0.0013 ( T 270 ) ) CN2 N2 N2
CCH CH CH
1
3
2
CCO2 CH CH
0.92 CCH CH CH
CCO2 CO2 CO2
1
3
2
CCO2 CO2 CH
0.92 CCO2 CO2 CO2
CCH CH CH
1
3
CCO2 N2 CH
1.10 CC02 CO2 CO2
CN2 N2 N2
CCH CH CH
After Bmix and Cmix are calculated, use following equation to solve for d:
2
P dRT 1 Bmix d Cmix d
P = absolute pressure
R = gas constant
Necessary input:
HV = volumetric gross heating value at reference conditions Th , Td, Pd
Gr = relative density (specific gravity) of mixture
xCO2 = mole fraction of carbon dioxide
HV. Z . R. Td 1
0 4
0
1.027 x10 Th 298.15
HN
Pd
HN0 = molar ideal gross heating value at 298.15K and 0.101325 MPa
Pd = reference pressure for molar density
R = gas constant, 8.31451 J/mol-K
Td = reference temperature for molar density
Th = reference temperature for heating value
Z0 = compressibility factor at reference conditions (set Z0=1 for initial iteration)
Gr Z R. Tgr ρ
0 0
air
Mr
Pgr
Mr = molar mass (molecular weight) of the mixture
Gr = relative density at reference conditions Tgr, Pgr
Pgr = reference pressure for relative density
Tgr = reference temperature for relative density
(ρ0)air = mass density of air at reference conditions Tgr, Pgr
0 M r ( air )
ρ Tgr , Pgr
air
R. Tgr
Bair Tgr
Pgr
Mr(air) = molar mass of air, 28.96256 g/mol
4 7 2
Bair Tgr .012527 5.91 x10 Tgr 6.62 x10 Tgr
0
Mr G2 HN M rN2 xCO2 M rN2 xCO2 M rCO2
xCH
G1 M rN2
xCH = mole fraction of equivalent hydrocarbon
G1 = -2.709328
G2 = 0.021062199
MrN2 = molar mass of nitrogen
MrCO2 = molar mass of carbon dioxide
0
Bmix Pgr
Z 1
new
R. Tgr
Repeat process, continuously replacing Z0 with (Z0) new, until (Z0/Z0new-1) is less than
the convergence criteria (5x10-11 in double precision or 5x10 -7 in single precision)
Necessary input:
Gr = relative density (specific gravity) of mixture
xCO2 = mole fraction of carbon dioxide
xN2 = mole fraction of nitrogen
Gr Z R. Tgr ρ
0 0
air
Mr
Pgr
0 M r ( air )
ρ Tgr , Pgr
air
R. Tgr
Bair Tgr
Pgr
0
Bmix Pgr
Z 1
new
R. Tgr
Repeat process, continuously replacing Z0 with (Z0) new, until (Z0/Z0new-1) is less than
the convergence criteria (5x10-11 in double precision or 5x10 -7 in single precision)
Symbol Definition
B Second virial coefficient
Bij Individual component interaction second virial coefficient
Bmix Second virial coefficient for the mixture
B`nij Binary characterization coefficient
Cijk Individual component interaction third virial coefficient
Cmix Third virial coefficient for the mixture
C`n Coefficient as a function of composition
d Molar density (moles per unit volume)
D Reduced density
Ei Characteristic energy parameter for ith component (Table 5)
Eij Second virial coefficient binary energy parameter
E`ij Second virial coefficient binary interaction parameter (Table 6)
F Mixture high temperature parameter
Fi High temperature parameter for ith component (Table 5)
G Orientation parameter
Gi Orientation parameter for ith component (Table 5)
Gij Binary orientation parameter
G`ij Binary interaction parameter for orientation (Table 6)
Gr Relative density (specific value) of mixture
HCH Molar gross heating value of the equivalent hydrocarbon
HN0 Molar ideal gross heating value at 298.15K and 0.101325 MPa
HV Volumetric gross heating value at reference conditions Th, Td, Pd
K Mixture size parameter
Ki Size parameter of ith component (Table 5)
Kij Binary interaction parameter for size (Table 6)
Mr Molar mass (molecular weight) of the mixture
Mr(air) Molar mass of air, 28.96256 g/mol
Mri Molar mass of ith component
N Number of components in the gas mixture
P Absolute pressure
Pd Reference pressure for molar density
Pgr Reference pressure for relative density
Q Quadrupole parameter
Qi Quadrupole parameter for ith component (Table 5)
R Gas constant, 8.31451 J/mol-K
r0air Mass density of air at reference conditions Tgr, Pgr
Si Dipole parameter for ith component (Table 5)
T Absolute temperature
Td Reference temperature for molar density
Tgr Reference temperature for relative density
Th Reference temperature for heating value
U Mixture energy parameter
Uij Binary interaction parameter for conformal energy (Table 6)
Wi Association parameter for ith component (Table 5)
xi Mole fraction of ith component
Z Compressibility factor
Z0 Compressibility factor at reference conditions
Z0new Compressibility factor for next iteration
an, bn, c n, fn, gn, k n, qn, sn, un, wn Constants given in Table 4
b0, b1, b2, c0, c1, c 2 Constants given in Table 7
bi0, bi1, bi2, c i0, c i1, ci2 Constants given in Table 8
2) Multiply this value for C d by the invariant A 1 to obtain new value of Re:
Ev Yd . 2 ρ f . ∆ P
2
A1
µf D
Re
A1
Cd
1 . 10
4
A1
For example:
1) at Re = ∞:
Cd = 0.9965
AGA 3, Orifice Metering of Natural Gas and Other Related Hydrocarbons, Part 1:
General Equations and Uncertainty Guidelines, 3rd ed., American Gas
Association, AGA Catalog No. XQ9210, Arlington, VA., 1990.
AGA 3, Orifice Metering of Natural Gas and Other Related Hydrocarbons, Part 2:
Specification and Installation Requirements, 4th ed., American Gas Association,
AGA Catalog No. XQ0002, Arlington, VA., 2000.
AGA 3, Orifice Metering of Natural Gas and Other Related Hydrocarbons, Part 3:
Natural Gas Applications, 3rd ed., American Gas Association,
AGA Catalog No. XQ9210, Arlington, VA., 1992.
AGA 3, Orifice Metering of Natural Gas and Other Related Hydrocarbons, Part :
Background, Development, Implementation Procedure, and Subroutine
Documentation for Empirical Flange-Tapped Discharge Coefficient Equation,
3rd ed., American Gas Association, AGA Catalog No. XQ9211, Arlington, VA.,
1992.
ASME: ASME International Steam Tables for Industrial Use, American Society of
Mechanical Engineers, New York, 2000.
GPA Standard 2145-00, Table of Physical Constants for Hydrocarbons and Other
Compounds of Interest to the Natural Gas Industry, Gas Producers Association,
Tulsa, OK., 2000.
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