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This document discusses equations of state (EOS) used to model the thermodynamic properties of fluids. It begins by defining an EOS as a mathematical relationship between pressure, volume, and temperature that fits experimental data. Ideal gas and virial EOS are introduced as simple models, with limitations. More complex cubic EOS like van der Waals, Redlich-Kwong, Soave-Redlich-Kwong, and Peng-Robinson are described, which can model both vapor and liquid states. These cubic EOS are expressed as polynomials that can be solved numerically or analytically to determine properties over a range of conditions. Examples are provided to demonstrate applications of the EOS.

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0% found this document useful (0 votes)
82 views37 pages

2 Cet

This document discusses equations of state (EOS) used to model the thermodynamic properties of fluids. It begins by defining an EOS as a mathematical relationship between pressure, volume, and temperature that fits experimental data. Ideal gas and virial EOS are introduced as simple models, with limitations. More complex cubic EOS like van der Waals, Redlich-Kwong, Soave-Redlich-Kwong, and Peng-Robinson are described, which can model both vapor and liquid states. These cubic EOS are expressed as polynomials that can be solved numerically or analytically to determine properties over a range of conditions. Examples are provided to demonstrate applications of the EOS.

Uploaded by

Muzammil Iqbal
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Chapter 2

Engineering Equations of State


for PvT properties

Equation of state

equation that relates measured variables


by fitting experimental data
mathematically: f(P,v,T) = 0
EOS can be precise in

P: P = f(T,v)
in v: v = f(T,P)
in z: z = Pv/RT = f(T,v)
in z: z = Pv/RT = f(T,P)
2

Ideal gas equation

Most common EOS: ideal gas model

P = RT/ v
Relates P, T and v
Derived directly from the kinetic theory of gases
Assumptions:

Molecules occupy no volume


Molecules exert no intermolecular forces

Generalization to non-ideality

Generalizing intermolecular interactions to


non-ideal behavior
Principle of corresponding state

The dimensionless potential energy is the same


for all species
Scale potential energy to the energy parameter
Example: critical point - a state determined by
intermolecular interaction characteristics of a
given species
Tr = T/Tc

Principle of corresponding
states

Two-parameter corresponding states

Three-parameter corresponding states

Two-parameter corresponding
states

says that all fluids when compared at the


same reduced temperature (Tr) and
reduced pressure (Pr), have approximately
the same compressibility factor, Z and all
deviate from ideal gas behavior to about the
same degree

Statement is based on non-polar species


6

Figure 3.1 Dashed lines are for methane, solid lines are for pentane.
The figure demonstrates that critical pressure and temperature alone
are insufficient to accurately represent the PvT behavior.

Three-parameter
corresponding states

However, different classes of molecules have


different intermolecular interactions (e.g.
polar vs. non-polar) and behaves differently
Therefore, additional parameter introduced:

Pitzer acentric factor,


characterizes how non-spherical a molecule is
is a way to class molecules according to
different characteristics
8

Three-parameter
corresponding states

says that all fluids having the same value


of acentric factor, when compared at the
same Tr and Pr, have about the same value
of Z and all deviate from ideal gas behavior
to about the same degree

The acentric factor, is defined with reference to its


vapor pressure. specifies a vapor pressure at a
reduced temperature of 0.7.

1.0 log Prsat

T r 0 .7

Psat at reduced
T of 0.7

Figure 3.2
Reduced vapor
pressure plotted
as a function of
reduced
temperature.
10

Generalized Compressibility
Factor Charts

PvT behavior can be generalized in terms of Tc, Pc


and . The correlation for Z is

Z Z 0 Z 1
Accounts
for simple
molecules

Correction factor for


the nonsphericity of
a species

Tables (Appendix C of textbook) or charts (Figure


4.14 of textbook) summarized the values of Z0 and
Z1 at reduced temperature and pressure. can be
found from Appendix A of your textbook.
11

Figure 3.3: Generalized


charts for estimating the
compressibility factor. The
plot of Z0 represents the
behaviour of a fluid that
would have =0. The plot
of Z1 is a correction factor
for
a
hypothetical
compound with =1.

12

Example 1: Application of the


generalized charts

Estimate the specific volume for CO2 at 310K and (a) 8 bars (b) 75
bars by the compressibility factor charts and compare to the
experimental values of 70.58 cm3/g and 3.9 cm3/g respectively.
Solution: = 0.228, Pc= 73.76 bar, Tc= 304.2 K
(a) Tr= 310/304.2= 1.02
Pr= 8/73.82= 0.108
From the charts, Z0= 0.96, Z1= 0,
Z= 0.96 + 0.228(0)= 0.96
v= ZRT/P
= ZRuT/PM
= [0.96*83.14cm3bar/molK*310 K]/[8 bar*44g/mol]
= 70.29 cm3/g (within 0.4 % of the experimental value)

13

Cont. Example 1

(b)

Tr= 310/304.2= 1.02

Pr= 75/73.76= 1.02

Interpolate between the reduced temperatures of 1.0 and 1.05.


At Tr= 1.0, Z0= 0.22, Z1= -0.08, therefore,
Z= 0.22 + 0.228*(-0.08)= 0.202
At Tr= 1.05, Z0= 0.58, Z1= 0.03, therefore,
Z= 0.58 + 0.228*(0.03)= 0.587
Interpolating, Z= 0.202 + (0.587-0.202)*0.02/0.05= 0.356
v= ZRT/P
= ZRuT/PM
= [0.356*83.14cm3bar/molK*310 K]/[75 bar*44g/mol]
= 2.78 cm3/g (giving 29% error relative to the experimental value)
14

The Virial Equation of State

At low pressure, the equation of state can be written


as explicit in a power series with respect to the
density.

Z 1 B C 2 D 3 ...

Derived from first


principles using
statistical
mechanics

B, C, D Virial
coefficients temperature
dependent only

C = D == 0 at low pressures
15

The virial equation is often


referred as:
Z 1 BP / RT or Z 1 B
where B T B B RT / P
0

B Pr / Tr

B 0 0.083 0.422 / Tr1.6


1

4.2
r

B 0.139 0.172 / T

Subject to Tr 0.686 0.439 Pr

or Vr 2.0
16

The Virial Equation of State

for vapor only


low pressures
obsolete
never use the virial equation

17

Example 2: Virial equation

Estimate the specific volume for CO2 at 310K and (a) 8 bars (b) 75 bars by
the virial equation and compare to the experimental values of 70.58 cm3/g
and 3.9 cm3/g respectively.

Solution: = 0.228, Pc= 73.82 MPa, Tc= 304.2 C


(a)
Tr= 310/304.2= 1.02
Pr= 8/73.82= 0.108
Check the applicability of virial equation
0.686 + (0.439*0.108)= 0.733<Tr
B0= 0.083 0.422/1.021.6= -0.326
B1= 0.139 0.172/1.024.2= -0.0193
Z= 1+[-0.326+(0.228*-0.0193]*0.108/1.02
Z= 0.965
v= ZRT/P
= ZRuT/PM
= [0.965*83.14cm3bar/molK*310 K]/[8 bar*44g/mol]
= 70.66 cm3/g (within 0.1 % of the experimental value)

18

Cont. Example 2
(b)

Tr= 310/304.2= 1.02

Pr= 75/73.82= 1.02

0.686 + (0.439*1.02)= 1.13>Tr


(virial equation not applicable)

19

Cubic equation of state

goes as a volume to the third power


hundreds of cubic EOS
provides reasonable values for both vapor
& liquid region
are approximates merely fit experimental
data

20

Cubic equation of state

Common Cubic EOS

Van der Waals EOS


Vapor only, low pressures

Redlich-Kwong EOS
Vapor only, moderate pressures

obsolete

Soave-Redlich-Kwong EOS
Vapor & saturated liquid, high pressures

Valuable in history
Nobody should use anymore

A very powerful equation used in industry

Peng-Robinson EOS
Vapor & saturated liquid, high pressures, HC industry std

Most commonly used in HC, better than SRK, a little more


complicated
21

Cubic equation of state

The general form of a cubic equation is


3 f1 (T , P ) 2 f 2 (T , P ) f 3 (T , P) 0

where fi(T,P) represents a function that can contain T,


P and fitting parameters

However, it is easier to solve cubic EOS in


3
2
the form of Z Z Z 0
22

Cubic equation of state

there are three roots for volume for fixed values of


T and P
meaning there are also 3 roots for Z
roots have different characteristics

Above critical point


1 positive real root
2 negative or imaginary numbers
Below critical point
3 real, positive roots
Lowest root liquid state
Highest root vapor state
Middle root throw out
23

van der Waals EOS

simplest form of the cubic EOS


P

RT
a
2
vb v

or

Z 1

b
a
1
a

1 b RT 1 b RT

Deviations due
to the repulsive
interactions

Deviations due
to the attractive
interactions

where
27 R 2Tc2
a
64 Pc

b 0.125 R

Tc
Pc
24

Redlich-Kwong EOS

The Redlich-Kwong EOS is given by


RT
a
P
1/ 2
b T ( b)
where
0.42728R 2Tc2.5
a
Pc
0.08664 RTc
b
Pc

25

Soave-Redlich Kuang EOS

is given by the equation:


RT
a
P

b ( b)
where

T
a a c 1 m 1
Tc

0.42747 R 2Tc2
ac
Pc

m 0.48508 1.55171 0.15613 2


0.08664 RTc
b
Pc

26

Soave-Redlich-Kwong EOS

written as a cubic polynomial:

Z 3 Z 2 Z 0
Where
-1
A B B2
-AB
A aP/(RT)2
B bP/RT
27

Example 3: SRK Equation

Use the SRK EOS to calculate for nButane at 500K and 30 bar
1. Z
2. v

28

29

30

Peng-Robinson EOS

is given by the equation


RT
a
P

b ( b) b( b)
where

T
a a c 1 m 1

0.45723553R 2Tc2
ac
Pc

m 0.37464 1.54226 0.26992 2


0.077796074RTc
b
Pc

31

Peng-Robinson EOS

written as a cubic polynomial:

Z 3 Z 2 Z 0
Where
B1
A 2B 3B2
B3 + B2 AB
A aP/(RT)2
B bP/RT
32

Figure 3.4 Comparison


of behavior of cubic in Z
for the PR-EOS at
several conditions.

P = Psat, T < Tc: The larger root of f(Z) is the vapor root. The
smallest root is the liquid root. The middle root corresponds to
a condition that violate thermodynamics stability.

P >> Psat, T < Tc: Compressed liquid, vapor root is less stable.

P << Psat, T < Tc: Superheated vapor, liquid root is less stable.

T > Tc: Supercritical fluid which can only have a single root.

33

17

The cubic equation can be solved by:


Iterative method such as the Newton-Raphson method
Analytical solution

1.

A summary of steps for iterative method:


Guess Zold=1 or Zold=0 and compute Fold(Zold)

2.

Compute dF/dZ

3.

Znew=Zold-F(Z)/(dF/dZ)

4.

If Z / Z new 1E 5 , print the value of Znew and stop

5.

Compute Fnew(Znew) and use this as Fold. Return to step 3


until step 4 terminates
An

initial guess of Z=0 converges on the smallest real root.


An initial guess of Z=1 converges on the largest real root.
At very high reduced pressures, an initial guess >1 may be required.

Example: Peng-Robinson
Equation

Use the Peng-Robinson EOS to


calculate for n-Butane at 500K and 30
bar
1. Z
2. v

35

Peng-Robinson EOS

Use the Peng-Robinson EOS to calculate for nButane at 500K and 30 bar

36

Example: Peng-Robinson
Equation

Estimate the specific volume for CO2 at 310K and (a) 8 bars (b) 75 bars by
the Peng-Robinson equation and compare to the experimental values of
70.58 cm3/g and 3.9 cm3/g respectively.
Solution: = 0.228, Pc= 73.82 MPa, Tc= 304.2 C
(a)
v= ZRT/P
= ZRuT/PM
= [0.961*83.14cm3bar/molK*310 K]/[8 bar*44g/mol]
= 70.36 cm3/g (within 0.3 % of the experimental value)

37

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