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Iapws If97 PDF
Iapws If97 PDF
Erlangen, Germany
September 1997
Release on the IAPWS Industrial Formulation 1997
for the Thermodynamic Properties of Water and Steam
1997 International Association for the Properties of Water and Steam
Publication in whole or in part is allowed in all countries provided that attribution is given to the
International Association for the Properties of Water and Steam
President:
Dr. R. Fernndez-Prini
Comisin Nacional de Energa Atmica
Av. Libertador 8250
Buenos Aires - 1429
Argentina
Executive Secretary:
Dr. R. B. Dooley
Electric Power Research Institute
3412 Hillview Avenue
Palo Alto, California 94304, USA
This release has been authorized by the International Association for the Properties of
Water and Steam (IAPWS) at its meeting in Erlangen, Germany, 14-20 September 1997, for
issue by its Secretariat. The members of IAPWS are Argentina, Canada, the Czech Republic,
Denmark, Germany, France, Italy, Japan, Russia, the United Kingdom, and the United States
of America.
The formulation provided in this release is recommended for industrial use, and is called
"IAPWS Industrial Formulation 1997 for the Thermodynamic Properties of Water and Steam"
abbreviated to "IAPWS Industrial Formulation 1997" (IAPWS-IF97). The IAPWS-IF97
replaces the previous industrial formulation "The 1967 IFC-Formulation for Industrial Use"
(IFC-67) [1]. Further details about the formulation can be found in the corresponding article
by W. Wagner et al. [2].
IAPWS also has a formulation intended for general and scientific use.
Further information about this release and other documents issued by IAPWS can be
obtained from the Executive Secretary of IAPWS.
Contents
1 Nomenclature
3 Reference Constants
6
9
10
11
12
13
17
20
22
26
29
32
33
34
35
39
39
40
42
42
44
12 Estimates of Uncertainties
45
13 References
48
1 Nomenclature
Thermodynamic quantities:
Superscripts:
cp
cv
o
r
Ideal-gas part
Residual part
f
g
h
M
p
R
Rm
s
T
u
v
w
x
b
g
d
D
h
q
J
p
r
s
t
f
Reducing quantity
Saturated liquid state
Saturated vapor state
Subscripts:
c
max
RMS
s
t
tol
Critical point
Maximum value
Root-mean-square value
Saturation state
Triple point
Tolerance of a quantity
Root-mean-square deviation:
D x RMS =
1 6
1
Dx
N
p 100 MPa
p 10 MPa .
Figure 1 shows the five regions into which the entire range of validity of IAPWS-IF97 is
divided. The boundaries of the regions can be directly taken from Fig. 1 except for the
boundary between regions 2 and 3; this boundary is defined by the so-called B23-equation
given in Section 4. Both regions 1 and 2 are individually covered by a fundamental equation
for the specific Gibbs free energy g( p,T ), region 3 by a fundamental equation for the specific
Helmholtz free energy f ( r,T ), where r is the density, and the saturation curve by a
saturation-pressure equation ps (T). The high-temperature region 5 is also covered by a g( p,T )
equation. These five equations, shown in rectangular boxes in Fig. 1, form the so-called basic
equations.
Regarding the main properties specific volume v, specific enthalpy h, specific isobaric heat
capacity cp , speed of sound w, and saturation pressure ps , the basic equations represent the
corresponding values from the "IAPWS Formulation 1995 for the Thermodynamic Properties
of Ordinary Water Substance for General and Scientific Use" [3] (hereafter abbreviated to
IAPWS-95) to within the tolerances specified for the development of the corresponding
equations; details of these requirements and their fulfillment are given in the comprehensive
paper on IAPWS-IF97 [2]. The basic equations for regions 1 and 3 also yield reasonable
values for the metastable states close to the stable regions. For region 2 there is a special
5
equation for the metastable-vapor region. Along the region boundaries the corresponding
basic equations are consistent with each other within specified tolerances; for details see
Section 10.
In addition to the basic equations, for regions 1, 2, and 4 so-called backward equations are
provided in form of T ( p,h ) and T ( p,s ) for regions 1 and 2, and Ts( p ) for region 4. These
backward equations are numerically consistent with the corresponding basic equations and
make the calculation of properties as functions of p,h and of p,s for regions 1 and 2, and of p
for region 4 extremely fast. In this way, properties such as T ( p,h ), h ( p,s ), and h( p ) can be
calculated without any iteration from the backward equation alone or by combination with the
corresponding basic equation, for example, h ( p,s ) via the relation h ( p,T ( p,s )). As a
consequence, the calculation of the industrially most important properties is on average more
than five times faster than the corresponding calculation with IFC-67; for details see
Section 11.
The estimates of uncertainty of the most relevant properties calculated from the
corresponding equations of IAPWS-IF97 are summarized in Section 12.
3 Reference Constants
The specific gas constant of ordinary water used for this formulation is
R = 0.461 526 kJ kg-1 K-1.
(1)
This value results from the recommended values of the molar gas constant [4], and the molar
mass of ordinary water [5, 6]. The values of the critical parameters
Tc = 647.096 K
pc = 22.064 MPa
rc = 322 kg m-3
(2)
(3)
(4)
(5)
6
Alternatively Eq. (5) can be expressed explicitly in temperature as
q = n4 + p n5 / n3
1/ 2
(6)
with q and p defined for Eq. (5) and the coefficients n3 to n5 listed in Table 1. Equations (5)
and (6) cover the range from 623.15 K at a pressure of 16.5292 MPa to 863.15 K at 100 MPa.
Table 1. Numerical values of the coefficients of the B23-equation, Eqs. (5) and (6), for
defining the boundary between regions 2 and 3
ni
ni
For computer-program verification, Eqs. (5) and (6) must meet the following T-p point:
T = 0.623 150 000 103 K , p = 0.165 291 643 102 MPa.
0 5 n 07.1 p 5 0t 1.2225
g( p, T )
= g p ,t =
RT
34
Ii
Ji
(7)
i =1
where p = p/p* and t = T */T with p* = 16.53 MPa and T * = 1386 K ; R is given by Eq. (1).
The coefficients ni and exponents Ii and Ji of Eq. (7) are listed in Table 2.
All thermodynamic properties can be derived from Eq. (7) by using the appropriate
combinations of the dimensionless Gibbs free energy and its derivatives. Relations between
the relevant thermodynamic properties and g and its derivatives are summarized in Table 3.
7
All required derivatives of the dimensionless Gibbs free energy are explicitly given in
Table 4.
Since the 5th International Conference on the Properties of Steam in London in 1956, the
specific internal energy and the specific entropy of the saturated liquid at the triple point have
been set equal to zero:
u t = 0 ; st = 0 .
(8)
In order to meet this condition at the temperature and pressure of the triple point
Tt = 273.16 K [8]
pt = 611.657 Pa [9] ,
(9)
the coefficients n3 and n4 in Eq. (7) have been adjusted accordingly. As a consequence, Eq. (7)
yields for the specific enthalpy of the saturated liquid at the triple point
h t = 0.611 783 J kg1 .
(10)
Table 2. Numerical values of the coefficients and exponents of the dimensionless Gibbs free energy
for region 1, Eq. (7)
Ii
Ji
Ii
18
19
17
20
21
22
23
24
25
10
26
10
27
11
11
28
12
29
21
29
13
30
23
31
14
31
29
38
15
32
30
39
16
33
31
40
17
34
32
41
ni
Ji
ni
0.441 418 453 308 46 105
8
Table 3. Relations of thermodynamic properties to the dimensionless Gibbs
free energy g and its derivatives a when using Eq. (7)
Property
Relation
Specific volume
v(p ,t )
v = g/ p
0 5
u p ,t
= t gt p g p
RT
u = g T g/ T
6 p(g/ p)
p
0 5
Specific entropy
s = g/ T
s p ,t
= t gt g
R
0 5
h p ,t
= t gt
RT
Specific enthalpy
h = g T g/ T
0 5 = t
c p p ,t
c p = h / T
0 5 = t
cv p , t
w = v ( p / v)s
gp =
g
! p
"# ,
#$t
gtt
gtt +
(g p t g pt )2
g pp
g p2
w 2 (p ,t )
=
RT
(g p t g pt )2
g pp
t 2g tt
Speed of sound
cv = u / T
p
= p gp
RT
1/ 2
g pp =
2g "# ,
! p 2 #$t
gt =
g
! t
"# ,
#$p
gtt =
2g "# ,
! t 2 #$p
g pt =
2g "#
! p t #$
Table 4. The dimensionless Gibbs free energy g and its derivatives a according to Eq. (7)
n 07.1 p 5 0t 1.2225
34
g=
Ii
Ji
i =1
34
gp =
ni Ii 7.1 p
i =1
0
34
gt =
ni 7.1 p
i =1
5 0t 1.2225
Ii 1
5 J 0t 1.2225
Ii
g pp =
gp =
g
! p
"# ,
#$t
g pp =
gtt =
i =1
n I 07.1 p 5
i i
2g "# ,
! p 2 #$t
Ii 2
34
Ji 1
Ii 1
i =1
i i
Ji
i =1
34
g pt =
n I 1 I 1607.1 p 5 0t 1.2225
34
Ji
gt =
g
! t
"# ,
#$p
Ji t 1.222
gtt =
Ji 1
2g "# ,
! t 2 #$p
g pt =
2g "#
! p t #$
Ji 2
9
Range of validity
Equation (7) covers region 1 of IAPWS-IF97 defined by the following range of
temperature and pressure; see Fig. 1:
273.15 K T 623.15 K
In addition to the properties in the stable single-phase liquid region, Eq. (7) also yields
reasonable values in the metastable superheated-liquid region close to the saturated liquid line.
Note: For temperatures between 273.15 K and 273.16 K at pressures below the melting pressure [10] (metastable states) all values are calculated by extrapolation from Eqs. (7) and (30).
Computer-program verification
To assist the user in computer-program verification of Eq. (7), Table 5 contains test values
of the most relevant properties.
Table 5. Thermodynamic property values calculated from Eq. (7) for selected values of T and p a
T = 300 K,
p = 3 MPa
T = 300 K,
p = 80 MPa
T = 500 K,
p = 3 MPa
v / (m3 kg1)
h / (kJ kg1)
u / (kJ kg1)
w / (m s1)
a It is recommended to verify programmed functions using 8 byte real values for all three combinations of T and
10
5.2.1 The Backward Equation T ( p, h )
The backward equation T ( p,h ) for region 1 has the following dimensionless form:
0 5 n p 0h + 15
T ( p, h)
= q p ,h =
T
20
Ii
Ji
(11)
i =1
where q = T/T *, p = p/p*, and h = h/h* with T * = 1 K , p* = 1 MPa, and h* = 2500 kJ kg-1.
The coefficients ni and exponents Ii and Ji of Eq. (11) are listed in Table 6.
Table 6. Numerical values of the coefficients and exponents of the backward equation T ( p,h ) for
region 1, Eq. (11)
Ii
Ji
ni
Ii
Ji
ni
11
12
10
13
32
14
10
22
15
32
32
16
10
17
32
18
32
19
32
10
20
32
Range of validity
Equation (11) covers the same range of validity as the basic equation, Eq. (7), except for
the metastable region (superheated liquid), where Eq. (11) is not valid.
Numerical consistency with the basic equation
For ten million random pairs of p and h covering the entire region 1, the differences T
between temperatures from Eq. (11) and from Eq. (7) were calculated and the absolute
maximum difference |T | max and the root-mean-square difference TRMS were determined.
These actual inconsistency values and the tolerated value |T | tol (see the beginning of
Section 5.2) amount to:
|T | tol = 25 mK ; TRMS = 13.4 mK ; |T | max = 23.6 mK .
(12)
11
Computer-program verification
To assist the user in computer-program verification of Eq. (11), Table 7 contains the
corresponding test values.
Table 7. Temperature values calculated from Eq. (11) for selected
values of p and h a
p / MPa
h/(kJ kg1)
T/K
500
80
500
80
1500
3
3
3
0 5 n p 0s + 25
T ( p, s)
= q p ,s =
T
20
Ii
Ji
(13)
i =1
where q = T/T *, p = p/p*, and s = s/s* with T * = 1 K , p* = 1 MPa, and s* = 1 kJ kg-1 K-1.
The coefficients ni and exponents Ii and Ji of Eq. (13) are listed in Table 8.
Table 8. Numerical values of the coefficients and exponents of the backward equation T ( p,s ) for
region 1, Eq. (13)
Ii
Ji
ni
Ii
Ji
11
12
12
31
13
14
11
15
31
16
17
31
18
10
19
32
10
20
32
ni
12
Range of validity
Equation (13) covers the same range of validity as the basic equation, Eq. (7), except for
the metastable region (superheated liquid), where Eq. (13) is not valid.
Numerical consistency with the basic equation
For ten million random pairs of p and s covering the entire region 1, the differences T
between temperatures from Eq. (13) and from Eq. (7) were calculated and the absolute
maximum difference |T | max and the root-mean-square difference TRMS were determined.
These actual differences and the tolerated value |T | tol (see the beginning of Section 5.2)
amount to:
|T | tol = 25 mK ; TRMS = 5.8 mK ; |T | max = 21.8 mK .
(14)
Computer-program verification
To assist the user in computer-program verification of Eq. (13), Table 9 contains the
corresponding test values.
Table 9.
p / MPa
1 1
s/(kJ kg K )
T/K
0.5
80
0.5
80
3
3
3
13
6.1 Basic Equation
The basic equation for this region is a fundamental equation for the specific Gibbs free
energy g. This equation is expressed in dimensionless form, g = g/( RT ), and is separated into
two parts, an ideal-gas part g o and a residual part g r, so that
0 5 0 5
0 5 0 5
g p, T
= g p , t = g o p , t + g r p ,t ,
RT
(15)
g = ln p +
o
niot Ji ,
(16)
i =1
where p = p/p* and t = T */T with p* = 1 MPa and T * = 540 K. The coefficients n 1o and n o2
were adjusted in such a way that the values for the specific internal energy and specific
entropy in the ideal-gas state relate to Eq. (8). Table 10 contains the coefficients nio and
exponents Jio of Eq. (16).
Table 10. Numerical values of the coefficients and exponents of the ideal-gas part g o of the
dimensionless Gibbs free energy for region 2, Eq. (16)a
Jio
nio
Jio
i
1
nio
a If Eq. (16) is incorporated into Eq. (18), instead of the values for n o and n o given above, the following values
1
2
for these two coefficients must be used: n 1o = 0.969 372 683 930 49 101 , n o2 = 0.100 872 759 700 06 102.
The form of the residual part g r of the dimensionless Gibbs free energy is as follows:
ni p I 0t 0.55 J
43
gr =
(17)
i =1
where p = p/p* and t = T */T with p* = 1 MPa and T * = 540 K. The coefficients ni and
exponents Ii and Ji of Eq. (17) are listed in Table 11.
14
Table 11. Numerical values of the coefficients and exponents of the
residual part g r of the dimensionless Gibbs free energy for
region 2, Eq. (17)
Ii
Ji
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
1
1
1
1
1
2
2
2
2
2
3
3
3
3
3
4
4
4
5
6
6
6
7
7
7
8
8
9
10
10
10
16
16
18
20
20
20
21
22
23
24
24
24
0
1
2
3
6
1
2
4
7
36
0
1
3
6
35
1
2
3
7
3
16
35
0
11
25
8
36
13
4
10
14
29
50
57
20
35
48
21
53
39
26
40
58
ni
15
All thermodynamic properties can be derived from Eq. (15) by using the appropriate
combinations of the ideal-gas part g o, Eq. (16), and the residual part g r, Eq. (17), of the
dimensionless Gibbs free energy and their derivatives. Relations between the relevant
thermodynamic properties and g o and g r and their derivatives are summarized in Table 12.
All required derivatives of the ideal-gas part and of the residual part of the dimensionless
Gibbs free energy are explicitly given in Table 13 and Table 14, respectively.
Table 12. Relations of thermodynamic properties to the ideal-gas part g o and the residual part g r of
the dimensionless Gibbs free energy and their derivatives a when using Eq. (15) or Eq. (18)
Property
Relation
p
= p g po + g pr
RT
Specific volume
v = g/ p T
v(p ,t )
u(p ,t )
= t gto + gtr - p g po + g pr
RT
Specific entropy
s = g/ T p
s p ,t
= t gto + gtr g o + g r
R
Specific enthalpy
h = g T g/ T p
h p ,t
= t gto + gtr
RT
c p p ,t
Speed of sound
w = v p / v
!
r
a g r = g
p
p
1/ 2
s
8 3
0 5 3
8 3
0 5 3
0 5 = t 3g
R
2
0 5
tt
+ gttr
r 2
cv p ,t
(1 + pg pr tpg pt
)
= t 2 gtto + gttr
2 r
R
1 p g pp
w 2 (p ,t )
=
RT
1 + 2pg pr + p 2g pr
r
1 p 2g pp
1 + pg
8 + 3 t 3g
r
r 2
p tpg pt
r
2 o
tt + gtt
16
Table 13. The ideal-gas part g o of the dimensionless Gibbs
free energy and its derivatives a according to
Eq. (16)
9
lnp
niot J
o
i
i =1
1/p
g po
o
g pp
= 1 / p 2
0
9
gto
nio Jiot Ji
i =1
o
g tt
o
g pt
o
i
i =1
o
a g o = g
p
Table 14. The residual part g r of the dimensionless Gibbs free energy and its derivatives a according
to Eq. (17)
ni p I 0t 0.55 J
43
g =
r
i =1
ni Ii p 0t 0.55
43
g pr
Ii 1
ni Ii 1 Ii 16p I 2 0t 0.55J
43
Ji
r
g pp
i =1
ni p Ji 0t 0.55
43
gtr
Ii
i =1
ni p I Ji 1 Ji 160t 0.55 J 2
43
Ji 1
gttr
i =1
i =1
ni Ii p I 1Ji 0t 0.55J 1
43
r
g pt
i =1
g pr =
g "# ,
! p #$t
r
r
g pp
=
2g "# ,
! p 2 #$t
r
gtr =
g "# ,
! t #$p
r
r
gtt
=
2g "# ,
! t 2 #$p
r
r
g pt
=
2g "#
! p t #$
r
17
Range of validity
Equation (15) covers region 2 of IAPWS-IF97 defined by the following range of
temperature and pressure, see Fig. 1:
273.15 K T 623.15 K
623.15 K < T 863.15 K
863.15 K < T 1 073.15 K
0 < p ps ( T )Eq.(30)
0 < p p ( T )Eq.(5)
0 < p 100 MPa
In addition to the properties in the stable single-phase vapor region, Eq. (15) also yields
reasonable values in the metastable-vapor region for pressures above 10 MPa. Equation (15)
is not valid in the metastable-vapor region at pressures p 10 MPa; for this part of the
metastable-vapor region see Section 6.2.
Note: For temperatures between 273.15 K and 273.16 K at pressures above the sublimation pressure [10]
(metastable states) all values are calculated by extrapolation from Eqs. (15) and (30).
Computer-program verification
To assist the user in computer-program verification of Eq. (15), Table 15 contains test
values of the most relevant properties.
Table 15. Thermodynamic property values calculated from Eq. (15) for selected values of T and p a
T = 300 K,
p = 0.0035 MPa
T = 700 K,
p = 0.0035 MPa
T = 700 K,
p = 30 MPa
v / (m3 kg1)
h / (kJ kg1)
u / (kJ kg1)
w / (m s1)
a It is recommended to verify programmed functions using 8 byte real values for all three combinations of T and
0 5 0 5
0 5 0 5,
g p, T
= g p ,t = g o p ,t + g r p ,t
RT
where p = p/p* and t = T */T with R given by Eq. (1).
(18)
18
The equation for the ideal-gas part g o is identical with Eq. (16) except for the values of the
two coefficients n 1o and n o2 , see Table 10. For the use of Eq. (16) as part of Eq. (18) the
coefficients n 1o and n o2 were slightly readjusted to meet the high consistency requirement
between Eqs. (18) and (15) regarding the properties h and s along the saturated vapor line; see
below.
The equation for the residual part g r reads
ni p I 0t 0.55J
13
g =
r
(19)
i =1
where p = p/p* and t = T */T with p* = 1 MPa and T * = 540 K. The coefficients ni and
exponents Ii and Ji of Eq. (19) are listed in Table 16.
Note: In the metastable-vapor region there are no experimental data to which an equation can be fitted. Thus,
Eq. (18) is only based on input values extrapolated from the stable single-phase region 2. These
extrapolations were performed with a special low-density gas equation [11] considered to be more suitable
for such extrapolations into the metastable-vapor region than IAPWS-95 [3].
Ii
Ji
ni
11
16
16
10
11
10
12
13
10
All thermodynamic properties can be derived from Eq. (18) by using the appropriate
combinations of the ideal-gas part g o, Eq. (16), and the residual part g r, Eq. (19), of the
dimensionless Gibbs free energy and their derivatives. Relations between the relevant
thermodynamic properties and g o and g r and their derivatives are summarized in Table 12.
19
All required derivatives of the ideal-gas part and of the residual part of the dimensionless
Gibbs free energy are explicitly given in Table 13 and Table 17, respectively.
Table 17. The residual part g r of the dimensionless Gibbs free energy and its derivatives a according
to Eq. (19)
ni p I 0t 0.55J
13
g =
r
i =1
ni Ii p 0t 0.55
13
g pr
Ii 1
r
g pp
i =1
13
gtr =
ni p Ii Ji t 0.5
i =1
ni Ii 1 Ii 16p I 2 0t 0.55J
13
Ji
i =1
ni p I Ji 1 Ji 160t 0.55 J 2
13
Ji 1
gttr =
i =1
ni Ii p I 1Ji 0t 0.55J 1
13
r
g pt
i =1
g pr =
g "# ,
! p #$t
r
r
g pp
=
2g "# ,
! p 2 #$t
r
gtr =
g "# ,
! t #$p
r
r
gtt
=
2g "# ,
! t 2 #$p
r
r
g pt
=
2g "#
! p t #$
r
Range of validity
Equation (18) is valid in the metastable-vapor region from the saturated vapor line to the
5 % equilibrium moisture line (determined from the equilibrium h and h values) at pressures
from the triple-point pressure, see Eq. (9), up to 10 MPa.
Consistency with the basic equation
The consistency of Eq. (18) with the basic equation, Eq. (15), along the saturated vapor line
is characterized by the following maximum inconsistencies regarding the properties v, h, cp , s,
g, and w :
|v| max = 0.014 %
|s| max = 0.082 J kg1 K1
|h| max = 0.043 kJ kg1 |g| max = 0.023 kJ kg1
|cp | max = 0.78 %
|w| max = 0.051 % .
These maximum inconsistencies are clearly smaller than the consistency requirements on
region boundaries corresponding to the so-called Prague values [13], which are given in
Section 10.
20
Along the 10 MPa isobar in the metastable-vapor region, the transition between Eq. (18)
and Eq. (15) is not smooth, which is however, not of importance for practical calculations.
Computer-program verification
To assist the user in computer-program verification of Eq. (18), Table 18 contains test
values of the most relevant properties.
Table 18. Thermodynamic property values calculated from Eq. (18) for selected values of T and p a
T = 450 K,
p = 1 MPa
v / (m3 kg1)
h / (kJ
kg1)
T = 440 K,
p = 1 MPa
T = 450 K,
p = 1.5 MPa
u / (kJ kg1)
w / (m s1)
a It is recommended to verify programmed functions using 8 byte real values for all three combinations of T and
21
In order to know whether the T( p,h ) equation for subregion 2b or for subregion 2c has to
be used for given values of p and h, a special correlation equation for the boundary between
subregions 2b and 2c (which approximates s = 5.85 kJ kg1 K1) is needed; see Fig. 2. This
boundary equation, called the B2bc-equation, is a simple quadratic pressure-enthalpy relation
which reads
p = n1 + n2h + n3h 2 ,
(20)
where p = p/p* and h = h/h* with p* = 1 MPa and h* = 1 kJ kg1. The coefficients n1 to n3 of
Eq. (20) are listed in Table 19. Based on its simple form, Eq. (20) does not describe exactly
the isentropic line s = 5.85 kJ kg-1 K1; the entropy values corresponding to this p-h relation
are between s = 5.81 kJ kg1 K1 and s = 5.85 kJ kg1 K1. The enthalpy-explicit form of
Eq. (20) is as follows:
h = n4 + p n5 / n3
1/ 2
(21)
with p and h according to Eq. (20) and the coefficients n3 to n5 listed in Table 19. Equations
(20) and (21) give the boundary line between subregions 2b and 2c from the saturation state at
T = 554.485 K and ps = 6.546 70 MPa to T = 1019.32 K and p = 100 MPa.
For the backward equations T( p,s ) the boundary between subregions 2b and 2c is, based
on the value s = 5.85 kJ kg1 K1 along this boundary, automatically defined for given values
of p and s.
22
Table 19. Numerical values of the coefficients of the B2bc-equation, Eqs. (20) and (21),
for defining the boundary between subregions 2b and 2c with respect to
T( p,h ) calculations
ni
1
2
ni
For computer-program verification, Eqs. (20) and (21) must meet the following p-h point:
p = 0.100 000 000 103 MPa , h = 0.351 600 432 3 104 kJ kg1.
6.3.1 The Backward Equations T( p, h ) for Subregions 2a, 2b, and 2c
The backward equation T( p,h ) for subregion 2a in its dimensionless form reads
0 5 n p 0h 2.15
T2 a ( p, h)
= q 2 a p ,h =
T
34
Ii
Ji
(22)
i =1
where q = T/T * , p = p/p* , and h = h/h* with T * = 1 K , p* = 1 MPa, and h* = 2000 kJ kg1.
The coefficients ni and exponents Ii and Ji of Eq. (22) are listed in Table 20.
Table 20. Numerical values of the coefficients and exponents of the backward equation T ( p,h ) for
subregion 2a, Eq. (22)
Ii
Ji
ni
Ii
Ji
ni
18
19
36
20
38
21
40
22
42
20
23
44
24
24
25
44
26
12
10
27
32
11
28
44
12
29
32
13
11
30
36
14
18
31
42
15
44
32
34
16
33
44
17
34
28
23
The backward equation T( p,h ) for subregion 2b in its dimensionless form reads
0 5 n 0p 25 0h 2.65
T2 b ( p, h)
= q 2 b p ,h =
T
38
Ii
Ji
(23)
i =1
where q = T/T *, p = p/p* , and h = h/h* with T * = 1 K , p* = 1 MPa, and h* = 2000 kJ kg1.
The coefficients ni and exponents Ii and Ji of Eq. (23) are listed in Table 21.
Table 21. Numerical values of the coefficients and exponents of the backward equation T ( p,h ) for
subregion 2b, Eq. (23)
Ii
Ji
ni
Ii
Ji
20
40
21
22
12
23
12
18
24
24
24
25
28
26
12
40
27
18
28
24
10
29
28
11
30
40
12
12
31
18
13
18
32
24
14
24
33
40
15
28
34
28
16
40
35
17
36
28
18
37
19
18
38
40
ni
24
The backward equation T( p,h ) for subregion 2c in its dimensionless form reads
0 5 n 0p + 255 0h 1.85
T2 c ( p, h)
= q 2 c p ,h =
T
23
Ii
Ji
(24)
i =1
where q = T/T *, p = p/p*, and h = h/h* with T * = 1 K , p* = 1 MPa, and h* = 2000 kJ kg1.
The coefficients ni and exponents Ii and Ji of Eq. (24) are listed in Table 22.
Table 22. Numerical values of the coefficients and exponents of the backward
equation T ( p,h ) for subregion 2c, Eq. (24)
Ii
Ji
ni
10
11
12
13
14
15
16
17
18
19
10
20
12
21
16
22
20
23
22
Range of validity
Equations (22), (23), and (24) are only valid in the respective subregion 2a, 2b, and 2c
which do not include the metastable-vapor region. The boundaries between these subregions
are defined at the beginning of Section 6.3; the lowest pressure for which Eq. (22) is valid
amounts to 611.153 Pa corresponding to the sublimation pressure [10] at 273.15 K.
25
Numerical consistency with the basic equation
For ten million random pairs of p and h covering each of the subregions 2a, 2b, and 2c, the
differences T between temperatures calculated from Eqs. (22) to (24), respectively, and from
Eq. (15) were determined. The corresponding maximum and root-mean-square differences are
listed in Table 23 together with the tolerated differences according to the numerical
consistency requirements with respect to Eq. (15).
Table 23. Maximum differences |T | max and root-mean-square differences TRMS between
temperatures calculated from Eqs. (22) to (24), and from Eq. (15) in comparison with the
tolerated differences |T | tol
Subregion
Equation
|T | tol /mK
|T | max /mK
TRMS /mK
2a
2b
2c
22
23
24
10
10
25
9.3
9.6
23.7
2.9
3.9
10.4
Computer-program verification
To assist the user in computer-program verification of Eqs. (22) to (24), Table 24 contains
the corresponding test values.
Table 24. Temperature values calculated from Eqs. (22) to (24) for
selected values of p and h a
Equation
22
23
24
p / MPa
h/(kJ kg1)
T/K
0.001
3000
3000
4000
3500
4000
25
3500
40
2700
60
2700
60
3200
for all three combinations of p and h given in this table for each of the equations.
26
6.3.2 The Backward Equations T( p, s ) for Subregions 2a, 2b, and 2c
The backward equation T( p,s ) for subregion 2a in its dimensionless form reads
0 5 n p 0s 25
T2 a ( p, s)
= q 2a p , s =
T
46
Ii
Ji
(25)
i =1
where q = T/T *, p = p/p*, and s = s/s* with T * = 1 K , p* = 1 MPa, and s* = 2 kJ kg1 K1.
The coefficients ni and exponents Ii and Ji of Eq. (25) are listed in Table 25.
Table 25. Numerical values of the coefficients and exponents of the backward equation T( p,s ) for
subregion 2a, Eq. (25)
Ii
Ji
ni
1.5
24
24 - 0.25
-11
1.5
23
25 - 0.25
-6
1.5
19
26
0.25
1.5
13
27
0.25
1.5
11
28
0.25
1.5
10
29
0.25
11
1.25
19
30
0.50
1.25
15
31
0.5
1.25
Ii
Ji
ni
32
0.5
105
33
0.5
10
1.0
26
11
1.0
21
34
0.5
10
12
1.0
17
35
0.5
14
13
1.0
16
36
0.5
16
14
1.0
37
0.75
15
1.0
38
0.75
16
0.75
15
39
0.75
17
0.75
14
40
0.75
17
18
0.5
26
41
1.0
19
0.5
13
42
1.0
18
20
0.5
43
1.25
21
0.5
44
1.25
15
22
0.25
27
45
1.5
23
0.25
25
46
1.5
18
27
The backward equation T( p,s ) for subregion 2b in its dimensionless form reads
0 5 n p 010 s 5
T2 b ( p, s )
= q 2 b p ,s =
T
44
Ii
Ji
(26)
i =1
where q = T/T *, p = p/p*, and s = s/s* with T * = 1 K , p* = 1 MPa, and s* = 0.7853 kJ kg1 K1.
The coefficients ni and exponents Ii and Ji of Eq. (26) are listed in Table 26.
Table 26. Numerical values of the coefficients and exponents of the backward equation T( p,s ) for
subregion 2b, Eq. (26)
Ii
Ji
ni
Ii
Ji
-6
-6
ni
23
11
24
-5
25
-5
11
26
-4
27
-4
28
-4
11
29
-3
30
-3
31
10
-3
11
32
11
-3
12
33
12
-2
34
13
-2
35
14
-2
36
15
-2
10
37
16
-1
38
17
-1
39
18
-1
40
19
-1
41
20
-1
42
21
43
22
44
28
The backward equation T( p,s ) for subregion 2c in its dimensionless form reads
0 5 n p 02 s 5
T2 c ( p, s )
= q 2c p ,s =
T
30
Ii
Ji
(27)
i =1
where q = T/T *, p = p/p*, and s = s/s* with T * = 1 K , p* = 1 MPa, and s* = 2.9251 kJ kg1 K1.
The coefficients ni and exponents Ii and Ji of Eq. (27) are listed in Table 27.
Table 27. Numerical values of the coefficients and exponents of the backward equation T( p,s ) for
subregion 2c, Eq. (27)
Ii
Ji
-2
-2
ni
Ii
Ji
ni
16
17
-1
18
19
20
21
22
23
24
10
25
11
26
12
27
13
28
14
29
15
30
Range of validity
Equations (25), (26), and (27) are only valid in the respective subregion 2a, 2b, and 2c
which do not include the metastable-vapor region. The boundaries between these subregions
are defined at the beginning of Section 6.3; the lowest pressure for which Eq. (25) is valid
amounts to 611.153 Pa corresponding to the sublimation pressure [10] at 273.15 K.
Numerical consistency with the basic equation
For ten million random pairs of p and s covering each of the subregions 2a, 2b, and 2c, the
differences T between temperatures calculated from Eqs. (25) to (27), respectively, and from
Eq. (15) were determined. The corresponding maximum and root-mean-square differences are
listed in Table 28 together with the tolerated differences according to the numerical
consistency requirements with respect to Eq. (15).
29
Table 28. Maximum differences |T | max and root-mean-square differences TRMS between
temperatures calculated from Eqs. (25) to (27), and from Eq. (15) in comparison with the
tolerated differences |T | tol
Subregion
Equation
|T | tol /mK
|T | max /mK
TRMS /mK
2a
2b
2c
25
26
27
10
10
25
8.8
6.5
19.0
1.2
2.8
8.3
Computer-program verification
To assist the user in computer-program verification of Eqs. (25) to (27), Table 29 contains
the corresponding test values.
Table 29. Temperature values calculated from Eqs. (25) to (27) for selected
values of p and s a
Equation
25
26
27
p / MPa
0.1
7.5
0.1
2.5
7.5
90
20
5.75
80
5.25
80
5.75
T/K
3
3
4
3
4
4
3
3
3
a It is recommended to verify the programmed equations using 8 byte real values for all
three combinations of p and s given in this table for each of the equations.
30
The basic equation for this region is a fundamental equation for the specific Helmholtz free
energy f. This equation is expressed in dimensionless form, f = f/(RT ), and reads
1 6
f (r, T )
= f d ,t = n1 ln d +
RT
40
ni d I t J ,
i
(28)
i=2
Ii
Ji
Ii
Ji
ni
101
21
ni
0.106 580 700 285 13
22
16
23
26
24
10
101
101
25
26
12
27
26
23
28
29
30
26
10
11
15
31
12
17
32
13
33
26
14
34
15
35
26
36
101
101
16
17
22
37
26
18
26
38
10
19
39
10
40
11
26
20
101
All thermodynamic properties can be derived from Eq. (28) by using the appropriate
combinations of the dimensionless Helmholtz free energy and its derivatives. Relations
between the relevant thermodynamic properties and f and its derivatives are summarized in
Table 31. All required derivatives of the dimensionless Helmholtz free energy are explicitly
given in Table 32.
31
Table 31. Relations of thermodynamic properties to the dimensionless Helmholtz
free energy f and its derivatives a when using Eq. (28)
Property
Relation
Pressure
p = r 2 f /r
1 6
p d ,t
= dfd
r RT
1 6
u d ,t
= t ft
RT
Specific entropy
s = f / T r
s d ,t
= t ft f
R
1 6
Specific enthalpy
h = f T f / T r + r f /r
1 6
h d ,t
= t ft + dfd
RT
1 6
cv d ,t
= t 2ftt
R
c p d ,t
Speed of sound
1/ 2
w = p/r s
dfd dtfdt
w 2 d ,t
= 2dfd + d 2fdd
RT
t 2ftt
ps
ps
;
= d fd d ,t
= d fd d ,t
RTr
RTr
1 6 = t
2df
ftt +
Phase-equilibrium condition
(Maxwell criterion)
2dfd + d 2fdd
1 6
dtfdt
0 5
0 5
p 1
1
= f 1d ,t 6 f 1d ,t 6
RT r r
f "# , f = f "# , f = f "#
=
! t $d
! t $d
! d t $
s
fd =
f "# , f = f "# , f
! d $t
! d $t
2
dd
tt
dt
Table 32. The dimensionless Helmholtz free energy equation and its derivatives a
according to Eq. (28)
40
f = n1 ln d +
ni d I t J
i
i=2
40
fd = n1 / d +
40
ft = 0 +
ni Ii d
Ii 1
40
fdd = n1 / d +
Ji
i=2
ni Ii 4 Ii 19 d I 2 t J
i
i=2
ni d I Ji 0 Ji 15 t J 2
40
ni d Ii Ji t Ji 1
ftt = 0 +
i=2
i=2
40
fdt = 0 +
a
fd =
ni Ii d I 1 Ji t J 1
i
i =2
dd
tt
dt
32
Range of validity
Equation (28) covers region 3 of IAPWS-IF97 defined by the following range of
temperature and pressure, see Fig. 1:
623.15 K T T ( p )Eq.(6)
In addition to the properties in the stable single-phase region defined above, Eq. (28) also
yields reasonable values in the metastable regions (superheated liquid and subcooled steam)
close to the saturated liquid and saturated vapor line.
Computer-program verification
To assist the user in computer-program verification of Eq. (28), Table 33 contains test
values of the most relevant properties.
Table 33. Thermodynamic property values calculated from Eq. (28), for selected values of T and r
T = 650 K,
r = 500 kg m3
T = 650 K,
r = 200 kg m3
T = 750 K,
r = 500 kg m3
p / MPa
h / (kJ kg1)
u / (kJ kg1)
w / (m s1)
a It is recommended to verify programmed functions using 8 byte real values for all three combinations of T and
(29)
33
b = ps / p
where
J=
and
1/ 4
(29a)
Ts
n9
+
T
Ts / T n10
(29b)
with p* = 1 MPa and T * = 1 K; for the coefficients n1 to n10 see Table 34.
8.1 The Saturation-Pressure Equation (Basic Equation)
The solution of Eq. (29) with regard to saturation pressure is as follows:
ps
p
2C
=
! B + 3 B 4 AC8
1/ 2
"#
##
$
(30)
A = J 2 + n1J + n2
B = n3J 2 + n4J + n5
C = n6J 2 + n7J + n8
with J according to Eq. (29b). The coefficients ni of Eq. (30) are listed in Table 34.
Table 34. Numerical values of the coefficients of the dimensionless saturation
equations, Eqs. (29) to (31)
ni
107
10
ni
Equations (29) to (31) reproduce exactly the p-T values at the triple point according to
Eq. (8), at the normal boiling point [12] and at the critical point according to Eqs. (2) and (3).
34
Range of validity
Equation (30) is valid along the entire vapor-liquid saturation line from the triple-point
temperature Tt to the critical temperature Tc and can be simply extrapolated to 273.15 K so
that it covers the temperature range
273.15 K T 647.096 K .
Computer-program verification
To assist the user in computer-program verification of Eq. (30), Table 35 contains test
values for three selected temperatures.
Table 35. Saturation pressures calculated from
Eq. (30) for selected values of T a
T/K
ps / MPa
300
500
600
Ts
=
T
6 1
1/ 2
where T * = 1 K and
D=
with
2G
F F 2 4 EG
1/ 2
E = b 2 + n3 b + n6
F = n1b 2 + n4 b + n7
G = n2 b 2 + n5 b + n8
and b according to Eq. (29a). The coefficients ni of Eq. (31) are listed in Table 34.
(31)
35
Range of validity
Equation (31) has the same range of validity as Eq. (30), which means that it covers the
vapor-liquid saturation line according to the pressure range
611.213 Pa p 22.064 MPa .
The value of 611.213 Pa corresponds to the pressure when Eq. (31) is extrapolated to 273.15 K.
Consistency with the basic equation
Since the saturation-pressure equation, Eq. (30), and the saturation-temperature equation,
Eq. (31), have been derived from the same implicit equation, Eq. (29), for describing the
saturation line, both Eq. (30) and Eq. (31) are completely consistent with each other.
Computer-program verification
To assist the user in computer-program verification of Eq. (31), Table 36 contains test
values for three selected pressures.
Table 36. Saturation temperatures calculated from
Eq. (31) for selected values of p a
p / MPa
Ts / K
0.1
10
36
0 5 0 5
0 5 0 5,
g p, T
= g p ,t = g o p ,t + g r p ,t
RT
(32)
g o = ln p +
niot J
o
i
(33)
i =1
where p = p/p* and t = T */T with p* = 1 MPa and T * = 1000 K. The coefficients n1o and n2o
were adjusted in such a way that the values for the specific internal energy and specific
entropy in the ideal-gas state relate to Eq. (8). Table 37 contains the coefficients nio and
exponents Jio of Eq. (33).
Table 37. Numerical values of the coefficients and exponents of the ideal-gas part g o of the
dimensionless Gibbs free energy for region 5, Eq. (33)
Jio
nio
Jio
nio
0.369 015 349 803 33
0.311 613 182 139 25 101
0.329 616 265 389 17
The form of the residual part g r of the dimensionless Gibbs free energy is as follows:
5
g =
r
ni p I t J
i
(34)
i =1
where p = p/p* and t = T */T with p* = 1 MPa and T * = 1000 K. The coefficients ni and
exponents Ii and Ji of Eq. (34) are listed in Table 38.
All thermodynamic properties can be derived from Eq. (32) by using the appropriate
combinations of the ideal-gas part g o, Eq. (33), and the residual part g r, Eq. (34), of the
dimensionless Gibbs free energy and their derivatives. Relations between the relevant
thermodynamic properties and g o and g r and their derivatives are summarized in Table 39.
All required derivatives of the ideal-gas part and of the residual part of the dimensionless
Gibbs free energy are explicitly given in Table 40 and Table 41, respectively.
37
Table 38. Numerical values of the coefficients and exponents of the
residual part g r of the dimensionless Gibbs free energy for
region 5, Eq. (34)
Ii
Ji
ni
Table 39. Relations of thermodynamic properties to the ideal-gas part g and the residual part g r of
the dimensionless Gibbs free energy and their derivatives a when using Eq. (32)
Property
Relation
p
= p g po + g pr
RT
Specific volume
v = g/ p T
v(p ,t )
u(p ,t )
= t gto + gtr - p g po + g pr
RT
Specific entropy
s = g/ T p
s p ,t
= t gto + gtr g o + g r
R
Specific enthalpy
h = g T g/ T p
h p ,t
= t gto + gtr
RT
c p p ,t
Speed of sound
w = v p / v
!
r
a g r = g
p
p
1/ 2
s
8 3
0 5 3
8 3
0 5 3
0 5 = t 3g
R
2
0 5
tt
+ gttr
r 2
cv p ,t
(1 + pg pr tpg pt
)
= t 2 gtto + gttr
2 r
R
1 p g pp
w 2 (p ,t )
=
RT
1 + 2pg pr + p 2g pr
r
1 p 2g pp
1 + pg
8 + 3 t 3g
r
r 2
p tpg pt
r
2 o
tt + gtt
38
Table 40. The ideal-gas part g o of the dimensionless Gibbs free
energy and its derivatives a according to Eq. (33)
6
lnp
niot Ji
i =1
g po
1/p
o
g pp
1 / p 2 +
0
6
gto
nio Jiot J 1
o
i
i =1
o
gtt
o
g pt
i =1
o
a g o = g
p
Table 41. The residual part g r of the dimensionless Gibbs free energy and its
derivatives a according to Eq. (34)
5
g =
r
ni p I t J
i
i =1
g pr =
r
g pp
=
i =1
ni p
Ii
Ji t
ni p I Ji 1 Ji 16 t J 2
5
Ji 1
gttr
i =1
i =1
r
g pt
ni Ii p I 1Ji t J 1
i
i =1
g pr =
g "# ,
! p #$t
r
i =1
gtr
ni Ii 1 Ii 16p I 2 t J
5
ni Ii p Ii 1 t Ji
r
g pp
=
2g "# ,
! p 2 #$t
r
gtr =
g "# ,
! t #$p
r
r
gtt
=
2g "# ,
! t 2 #$p
r
r
g pt
=
2g "#
! p t #$
r
39
Range of validity
Equation (32) covers region 5 of IAPWS-IF97 defined by the following temperature and
pressure range:
1073.15 K T 2273.15 K
0 < p 10 MPa .
In this range Eq. (32) is only valid for pure undissociated water, any dissociation will have to
be taken into account separately.
Computer-program verification
To assist the user in computer-program verification of Eq. (32), Table 42 contains test
values of the most relevant properties.
Table 42. Thermodynamic property values calculated from Eq. (32) for selected values of T and p a
T = 1500 K,
p = 0.5 MPa
T = 1500 K,
p = 8 MPa
v / (m3 kg1)
kg1)
104
h / (kJ
T = 2000 K,
p = 8 MPa
0.115 743 146
104
u / (kJ kg1)
w / (m s1)
a It is recommended to verify programmed functions using 8 byte real values for all three combinations of T and
40
Equations (15) and (28) with respect to the boundary between regions 2 and 3 defined by
the B23-equation, Eq. (5), for temperatures between 623.15 K and 863.15 K.
Equations (15) and (32) with respect to the 1073.15 K isotherm for p 10 MPa
corresponding to the boundary between regions 2 and 5.
The results of the consistency investigations for these three region boundaries are
summarized in Table 43. In addition to the permitted inconsistencies corresponding to the
Prague values [13], the actual inconsistencies characterized by their maximum and root-meansquare values, xmax and x RMS , along the three boundaries are given for x = v, h, cp , s, g,
and w. It can be seen that the inconsistencies between the basic equations along the
corresponding region boundaries are extremely small.
Table 43. Inconsistencies between basic equations for single-phase regions at the joint region
boundary
Inconsistency
x
Prague
value
Regions 1/3
Eqs. (7)/(28)
Regions 2/3
Eqs. (15)/(28)
Regions 2/5
Eqs. (15)/(32)
xmax x RMS a
v/%
0.05
0.004
0.002
0.018
0.007
0.002
0.001
h/(kJ kg1)
0.2
0.031
0.014
0.134
0.073
0.020
0.012
cp/%
0.195
0.058
0.353
0.169
0.081
0.048
0.2
0.042
0.022
0.177
0.094
0.042
0.025
g/(kJ kg1)
0.2
0.005
0.005
0.005
0.003
0.026
0.021
0.299
0.087
0.403
0.073
0.021
0.009
w/%
1b
a The x
RMS values (see Nomenclature) were calculated from about 10 000 points evenly distributed along the
corresponding boundary.
b The permitted inconsistency value for w is not included in the Prague values.
41
D ps = ps, Eq.(7), Eq.(15) ps, Eq.(30)
DTs = Ts, Eq.(7), Eq.(15) Ts, Eq.(31)
Dg = g Eq.(7)
g Eq.(15)
(35a)
(35b)
(35c)
The calculation of ps and of Ts from Eqs. (7) and (15) is made via the Maxwell criterion
(phase-equilibrium condition) for given values of T or p. The g values are determined for
given T values and corresponding ps values from Eq. (30).
Equations (28) and (30) on the saturation line for temperatures from 623.15 K to
Tc = 647.096 K.
D ps = ps, Eq.(28)
ps, Eq.(30)
DTs = Ts, Eq.(28)
Ts, Eq.(31)
Dg = gEq.(28), Eq.(30) gEq.(28), Eq.(30)
(36a)
(36b)
(36c)
The calculation of ps and Ts from Eq. (28) is made via the Maxwell criterion for given
temperatures or pressures, respectively. The inconsistency Dg corresponds to the difference
g( r , T ) - g( r , T ) which is calculated from Eq. (28) after r and r are determined from
Eq. (28) by iteration for given T values and corresponding ps values from Eq. (30).
Equations (7), (15) and (28) on the saturation line at 623.15 K. This is the only point on the
saturation line where the validity ranges of the fundamental equations of regions 1 to 3
meet each other.
D ps = ps, Eq.(7), Eq.(15) ps, Eq.(28)
(37a)
(37b)
Dg = g Eq.(7), Eq.(15)
g Eq.(28)
(37c)
All three properties ps and Ts and g are calculated via the Maxwell criterion from the
corresponding equations.
The results of these consistency investigations along the saturation line are summarized in
Table 44. In addition to the permitted inconsistencies corresponding to the Prague values [13],
the actual inconsistencies characterized by their maximum and root-mean-square values,
xmax and x RMS , for the two sections of the saturation line are given for x = ps , Ts and g.
It can be seen that the inconsistencies between the basic equations for the corresponding singlephase region and the saturation-pressure equation are extremely small. This statement also
holds for the fundamental equations, Eqs. (7), (15), and (28), among one another and not only
in relation to the saturation-pressure equation, Eq. (30), see the last column in Table 44.
42
Table 44. Inconsistencies between the basic equations valid at the saturation line
Inconsistency
x
ps/%
Ts/%
g/(kJ
kg1)
Prague
value
Tt T 623.15 K
Eqs. (7),(15)/(30)
623.15 K T Tc
Eqs. (28)/(30)
xmax xRMS a
xmax xRMS a
T = 623.15 K
Eqs. (7),(15)/(28)
0.05
0.0069
0.0033
0.0026
0.0015
0.0041
0.02
0.0006
0.0003
0.0003
0.0002
0.0006
0.2
0.012
0.006
0.002
0.001
0.005
a The x
RMS values (see Nomenclature) were calculated from about 3000 points evenly distributed along the two
43
frequencies of use have to be taken into account. The total CTR value was calculated as
follows: As has been described before, the computing times for each function were
determined for IFC-67 and for IAPWS-IF97. Then, these values were weighted by the
corresponding frequencies of use and added up for the 16 functions of the three regions. The
total CTR value is obtained from the sum of the weighted computing times for IFC-67 divided
by the corresponding value for IAPWS-IF97. The total CTR value for regions 1, 2, and 4
amounts to
CTR regions 1, 2, 4 = 5.1 .
(38)
This means that for regions 1, 2, and 4 together the property calculations with IAPWS-IF97
are more than five times faster than with IFC-67.
Table 45. Results of the computing-time investigations of IAPWSIF97 in relation to IFC-67 for regions 1, 2, and 4 a
Region
Function
Frequency
of use
%
Computing-time
ratio
IFC-67 / IF97
v ( p, T )
h ( p, T )
T ( p, h )
h ( p, s )
2.9
9.7
3.5
1.2
2.7
2.9
24.8
10.0
S region 1: 5.6 c
v ( p, T )
h ( p, T )
s ( p, T )
T ( p, h )
v ( p, h )
s ( p, h )
T ( p, s )
h ( p, s )
6.1
12.1
1.4
8.5
3.1
1.7
1.7
4.9
2.1
2.9
1.4
12.4
6.4
4.2
8.1
5.6
S region 2: 5.0 c
ps( T )
Ts( p )
h( p )
h( p )
8.0
30.7
2.25
2.25
1.7
5.6
4.4
4.2
S region 4: 4.9 c
S regions 1, 2 and 4: 5.1 c
a Based on the agreed PC Intel 486 DX 33 with MS Fortran 5.1 compiler.
b For the definition of the regions see Fig. 1.
c This CTR value is based on the computing times for the single
44
Table 45 also contains total CTR values separately for each of regions 1, 2, and 4. In
addition, CTR values for each single function are given. When using IAPWS-IF97 the
functions depending on p,h and p,s for regions 1 and 2 and on p for region 4 were calculated
from the backward equations alone (functions explicit in T ) or from the basic equations in
combination with the corresponding backward equation.
If a faster processor than specified above is used for the described benchmark tests, similar
CTR values are obtained. A corresponding statement is also valid for other compilers than the
specified one.
11.2 Computing-Time Investigations for Regions 3 and 5
For regions 3 and 5 the CTR values only relate to single functions and are given by the
quotient of the computing time needed for IFC-67 calculation and the computing time when
using IAPWS-IF97; there are no frequency-of-use values for functions relevant to these two
regions.
For region 3 of IAPWS-IF97, corresponding to regions 3 and 4 of IFC-67, the computingtime investigations relate to the functions p ( v, T ), h ( v, T ), cp ( v, T ), and s ( v, T ) where 10 % of
the test points are in region 4 of IFC-67. For region 5 of IAPWS-IF97, the computing-time
investigations relate only to the functions v ( p, T ), h ( p, T ), and cp ( p, T ), where the CTR
values were determined for 1073.15 K, the maximum temperature for which IFC-67 is valid.
Table 46 lists the CTR values obtained for the relevant functions of regions 3 and 5.
Roughly speaking, IAPWS-IF97 is more than three times faster than IFC-67 for region 3 and
more than nine times faster for the 1073.15 K isotherm where region 5 overlaps IFC-67.
Table 46. Results of the computing-time investigations of IAPWS-IF97 in relation to IFC-67
for regions 3 and 5 a
Region
Function
p ( v, T )
h ( v, T )
cp ( v, T )
s ( v, T )
v ( p, T )
h ( p, T )
cp ( p, T )
Computing time
ratio
IFC-67 / IF97
3.8
4.3
2.9
3.2
8.9 c
11.9 c
15.8 c
compiler.
b For the definition of the regions see Fig. 1.
c Determined for the 1073.15 K isotherm for which IFC-67 is
valid.
45
12 Estimates of Uncertainties
Estimates have been made of the uncertainty of the specific volume, specific isobaric heat
capacity, speed of sound, and saturation pressure when calculated from the corresponding
equations of IAPWS-IF97. These estimates were derived from the uncertainties of
IAPWS-95 [3], from which the input values for fitting the IAPWS-IF97 equations were
calculated, and in addition by taking into account the deviations between the corresponding
values calculated from IAPWS-IF97 and IAPWS-95. Since there is no reasonable basis for
estimating the uncertainty of specific enthalpy (because specific enthalpy is dependent on the
selection of the zero point, only enthalpy differences of different size are of interest), no
uncertainty is given for this property. However, the uncertainty of isobaric enthalpy differences
is smaller than the uncertainty in the isobaric heat capacity.
For the single-phase region, tolerances are indicated in Figs. 3 to 5 which give the estimated
uncertainties in various areas. As used here "tolerance" means the range of possible values as
judged by IAPWS, and no statistical significance can be attached to it. With regard to the
uncertainty for the speed of sound and the specific isobaric heat capacity, see Figs. 4 and 5, it
should be noted that the uncertainties for these properties increase drastically when approaching
the critical point. The statement "no definitive uncertainty estimates possible" for temperatures
above 1273 K is based on the fact that this range is beyond the range of validity of IAPWS-95
and the corresponding input values for IAPWS-IF97 were extrapolated from IAPWS-95. From
various tests of IAPWS-95 [3] it is expected that these extrapolations yield reasonable values.
For the saturation pressure, the estimate of uncertainty is shown in Fig. 6.
46
Fig. 3. Uncertainties in specific volume, Dv /v, estimated for the corresponding equations of IAPWS-IF97. In the
enlarged critical region (triangle), the uncertainty is given as percentage uncertainty in pressure, Dp/p.
This region is bordered by the two isochores 0.0019 m3 kg-1 and 0.0069 m3 kg-1 and by the 30 MPa
isobar. The positions of the lines separating the uncertainty regions are approximate.
Fig. 4. Uncertainties in specific isobaric heat capacity, Dcp /cp, estimated for the corresponding equations of
IAPWS-IF97. For the definition of the triangle around the critical point, see Fig. 3. The positions of the
lines separating the uncertainty regions are approximate.
47
Fig. 5. Uncertainties in speed of sound, Dw/w, estimated for the corresponding equations of IAPWS-IF97. For
the definition of the triangle around the critical point, see Fig. 3. The positions of the lines separating the
uncertainty regions are approximate.
Fig. 6. Uncertainties in saturation pressure, Dps /ps, estimated for the saturation-pressure equation, Eq. (30).
48
13 References
[1]
[2]
Wagner, W., Cooper, J. R., Dittmann, A., Kijima, J., Kretzschmar, H.-J., Kruse, A., Mare, R.,
Oguchi, K., Sato, H., Stcker, I., ifner, O., Takaishi, Y., Tanishita, I., Trbenbach, J., and
Willkommen, Th., The IAPWS Industrial Formulation 1997 for the Thermodynamic Properties
of Water and Steam, to be submitted for publication.
[3]
IAPWS Release on the IAPWS Formulation 1995 for the Thermodynamic Properties of
Ordinary Water Substance for General and Scientific Use, IAPWS Secretariat 1996.
[4]
Cohen, E. R. and Taylor, B. N., The 1986 Adjustment of the Fundamental Physical Constants,
CODATA Bulletin No. 63, Committee on Data for Science and Technology, Int. Council of
Scientific Unions, Pergamon Press, Oxford, 1986.
[5]
Audi, G. and Wapstra, A. H., The 1993 atomic mass evaluation, (I) Atomic mass table, Nuclear
Physics A 565 (1993), 1-65.
[6]
IUPAC Commission on the Atomic Weights and Isotopic Abundances, Subcommittee for
Isotopic Abundance Measurements, Isotopic compositions of the elements 1989, Pure and
Appl. Chem. 63 (1991), 991-1002.
[7]
IAPWS Release on the Values of Temperature, Pressure and Density of Ordinary and Heavy
Water Substances at Their Respective Critical Points, in Physical Chemistry of Aqueous
Systems: Meeting the Needs of Industry, edited by H. J. White, Jr. et al., Proceedings of the
12th International Conference on the Properties of Water and Steam, pp. A 101 - A 102, Begell
House, New York, 1995.
[8]
[9]
Guildner, L. A., Johnson, D. P., and Jones, F. E., Vapor Pressure of Water at Its Triple Point,
J. Res. Natl. Bur. Stand. 80A (1976), 505-521.
[10] IAPWS Release on the Pressure along the Melting and Sublimation Curves of Ordinary Water
Substance, in Wagner, W., Saul, A., and Pru, A., J. Phys. Chem. Ref. Data 23, 515-527
(1994), also in Physical Chemistry of Aqueous Systems: Meeting the Needs of Industry, edited
by H. White, Jr. et al., Proceedings of the 12th International Conference on the Properties of
Water and Steam, pp. A 9 - A 12, Begell House, New York, 1995.
[11] Pru, A. and Wagner, W., New International Formulation for the Thermodynamic Properties of
Ordinary Water Substance for General and Scientific Use, to be submitted to J. Phys. Chem.
Ref. Data (1997).
[12] IAPWS Supplementary Release on Saturation Properties of Ordinary Water Substance, in
Wagner, W. and Pru, A., J. Phys. Chem. Ref. Data 22, 783-787 (1993), also in Physical
Chemistry of Aqueous Systems: Meeting the Needs of Industry, edited by H. White, Jr. et al.,
Proceedings of the 12th International Conference on the Properties of Water and Steam, pp.
A 143-A 149, Begell House, New York, 1995.
[13] Minutes of the meetings of the International Formulation Committee of ICPS in Prague, 1965.
[14] McClintock, R. B. and Silvestri, G. J., Formulations and iterative procedures for the
calculation of properties of steam, The American Society of Mechanical Engineers, New York,
1968.