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Water gas shift equilibria via the NIST Webbook

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Water gas shift equilibria via the NIST Webbook John Kitchin The NIST webbook provides parameterized models of the enthalpy, entropy and heat capacity of many molecules. In this example, we will examine how to use these to compute the equilibrium constant for the water gas shift reaction range of 500K to 1000K. Parameters are provided for: in the temperature

Contents Setup equations for each species Hydrogen H2O CO CO2 Standard state heat of reaction Correcting Plot how the
$\Delta G$

and
$\Delta G$

varies with temperature

Equilibrium constant calculation Equilibrium yield of WGS Compute gas phase pressures of each species Compare the equilibrium constants Summary

Cp = heat capacity (J/mol*K) H = standard enthalpy (kJ/mol) S = standard entropy (J/mol*K)

with models in the form:

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where

, and

is the temperature in Kelvin. We can use this data to calculate equilibrium constants in the following manner. First,

we have heats of formation at standard state for each compound; for elements, these are zero by definition, and for non-elements, they have values available from the NIST webbook. There are also values for the absolute entropy at standard state. Then, we have an expression for the change in enthalpy from standard state as defined above, as well as the absolute entropy. From these we can derive the reaction enthalpy, free energy and entropy at standard state, as well as at other temperatures. We will examine the water gas shift enthalpy, free energy and equilibrium constant from 500K to 1000K, and finally compute the equilibrium composition of a gas feed containing 5 atm of CO and H2 at 1000K.

close all; clear all; clc; T = linspace(500,1000); % degrees K t = T/1000;

Setup equations for each species First we enter in the parameters and compute the enthalpy and entropy for each species. Hydrogen link

% T = 298-1000K valid temperature range A = 33.066178; B = -11.363417; C = 11.432816; D = -2.772874; E = -0.158558; F = -9.980797; G = H = 172.707974; 0.0;

Hf_29815_H2 = 0.0; % kJ/mol S_29815_H2 = 130.68; % J/mol/K dH_H2 = A*t + B*t.^2/2 + C*t.^3/3 + D*t.^4/4 - E./t + F - H; S_H2 = (A*log(t) + B*t + C*t.^2/2 + D*t.^3/3 - E./(2*t.^2) + G);

H2O link Note these parameters limit the temperature range we can examine, as these parameters are not valid below 500K. There is another set of parameters for lower temperatures, but we do not consider them here.

% 500-1700 K valid temperature range A = B = C = D = E = F = G = H = 30.09200; 6.832514; 6.793435; -2.534480; 0.082139; -250.8810; 223.3967; -241.8264;

Hf_29815_H2O = -241.83; %this is Hf. S_29815_H2O = 188.84; dH_H2O = A*t + B*t.^2/2 + C*t.^3/3 + D*t.^4/4 - E./t + F - H; S_H2O = (A*log(t) + B*t + C*t.^2/2 + D*t.^3/3 - E./(2*t.^2) + G);

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CO link

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% 298. - 1300K valid temperature range A = B = C = D = E = F = G = 25.56759; 6.096130; 4.054656; -2.671301; 0.131021; -118.0089; 227.3665;

H = -110.5271; Hf_29815_CO = -110.53; %this is Hf kJ/mol. S_29815_CO = 197.66; dH_CO = A*t + B*t.^2/2 + C*t.^3/3 + D*t.^4/4 - E./t + F - H; S_CO = (A*log(t) + B*t + C*t.^2/2 + D*t.^3/3 - E./(2*t.^2) + G);

CO2 link

% 298. - 1200.K valid temperature range A = 24.99735; B = C = D = E = F = G = H = 55.18696; -33.69137; 7.948387; -0.136638; -403.6075; 228.2431; -393.5224;

Hf_29815_CO2 = -393.51; %this is Hf. S_29815_CO2 = 213.79; dH_CO2 = A*t + B*t.^2/2 + C*t.^3/3 + D*t.^4/4 - E./t + F - H; S_CO2 = (A*log(t) + B*t + C*t.^2/2 + D*t.^3/3 - E./(2*t.^2) + G);

Standard state heat of reaction We compute the enthalpy and free energy of reaction at 298.15 K for the following reaction .

Hrxn_29815 = Hf_29815_CO2 + Hf_29815_H2 - Hf_29815_CO - Hf_29815_H2O; Srxn_29815 = S_29815_CO2 + S_29815_H2 - S_29815_CO - S_29815_H2O; Grxn_29815 = Hrxn_29815 - 298.15*(Srxn_29815)/1000; sprintf('deltaH = %1.2f',Hrxn_29815) sprintf('deltaG = %1.2f',Grxn_29815)

ans = deltaH = -41.15

ans = deltaG = -28.62

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Correcting and

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we have to correct for temperature change away from standard state. We only correct the enthalpy for this temperature change. The correction looks like this:

Where

are the stoichiometric coefficients of each species, with appropriate sign for reactants and products, and

is

precisely what is calculated for each species with the equations

Hrxn = Hrxn_29815 + dH_CO2 + dH_H2 - dH_CO - dH_H2O;

The entropy is on an absolute scale, so we directly calculate entropy at each temperature. Recall that H is in kJ/mol and S is in J/mol/K, so we divide S by 1000 to make the units match.

Grxn = Hrxn - T.*(S_CO2 + S_H2 - S_CO - S_H2O)/1000;

Plot how the

varies with temperature

over this temperature range the reaction is exothermic, although near 1000K it is just barely exothermic. At higher temperatures we expect the reaction to become endothermic.

figure; hold all plot(T,Grxn) plot(T,Hrxn) xlabel('Temperature (K)') ylabel('(kJ/mol)') legend('\Delta G_{rxn}', '\Delta H_{rxn}', 'location','best')

Equilibrium constant calculation Note the equilibrium constant starts out high, i.e. strongly favoring the formation of products, but drops very quicky with increasing temperature.

R = 8.314e-3; %kJ/mol/K K = exp(-Grxn/R./T);

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figure plot(T,K) xlim([500 1000]) xlabel('Temperature (K)') ylabel('Equilibrium constant')

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Equilibrium yield of WGS Now lets suppose we have a reactor with a feed of H2O and CO at 10atm at 1000K. What is the equilibrium yield of H2? Let be the extent of reaction, so that . For reactants, is negative, and for products, is positive. We have to solve for the extent of reaction that

satisfies the equilibrium condition.

A = CO B = H2O C = H2 D = CO2

Pa0 = 5; Pb0 = 5; Pc0 = 0; Pd0 = 0; R = 0.082; Temperature = 1000;

% pressure in atm

% we can estimate the equilibrium like this. We could also calculate it % using the equations above, but we would have to evaluate each term. Above % we simple computed a vector of enthalpies, entropies, etc... K_Temperature = interp1(T,K,Temperature); % If we let X be fractional conversion then we have $C_A = C_{A0}(1-X)$, % $C_B = C_{B0}-C_{A0}X$, $C_C = C_{C0}+C_{A0}X$, and $C_D = % C_{D0}+C_{A0}X$. We also have $K(T) = (C_C C_D)/(C_A C_B)$, which finally % reduces to $0 = K(T) - Xeq^2/(1-Xeq)^2$ under these conditions. f = @(X) K_Temperature - X^2/(1-X)^2; Xeq = fzero(f,[1e-3 0.999]); sprintf('The equilibrium conversion for these feed conditions is: %1.2f',Xeq)

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ans = The equilibrium conversion for these feed conditions is: 0.55

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Compute gas phase pressures of each species Since there is no change in moles for this reaction, we can directly calculation the pressures from the equilibrium conversion and the initial pressure of gases. you can see there is a slightly higher pressure of H2 and CO2 than the reactants, consistent with the equilibrium constant of about 1.44 at 1000K. At a lower temperature there would be a much higher yield of the products. For example, at 550K the equilibrium constant is about 58, and the pressure of H2 is 4.4 atm due to a much higher equilibrium conversion of 0.88.

P_CO = Pa0*(1-Xeq) P_H2O = Pa0*(1-Xeq) P_H2 = Pa0*Xeq P_CO2 = Pa0*Xeq

P_CO = 2.2748

P_H2O = 2.2748

P_H2 = 2.7252

P_CO2 = 2.7252

Compare the equilibrium constants We can compare the equilibrium constant from the Gibbs free energy and the one from the ratio of pressures. They should be the same!

K_Temperature (P_CO2*P_H2)/(P_CO*P_H2O)

K_Temperature = 1.4352

ans = 1.4352

Summary The NIST Webbook provides a plethora of data for computing thermodynamic properties. It is a little tedious to enter it all into Matlab, and a little tricky to use the data to estimate temperature dependent reaction energies. A limitation of the Webbook is that it does not tell you have the thermodynamic properties change with pressure. Luckily, those changes tend to be small.

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% categories: Miscellaneous, nonlinear algebra % tags: thermodynamics, reaction engineering

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Related posts: 1. Constrained minimization to find equilibrium compositions 2. Numerically calculating an effectiveness factor for a porous catalyst bead This entry was posted in Miscellaneous, Nonlinear algebra and tagged reaction engineering, thermodynamics by John Kitchin. Bookmark the permalink [http://matlab.cheme.cmu.edu/2011/12/12/water-gas-shift-equilibria-via-the-nist-webbook/] .
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