In: Chemistry
calculate the partial pressure of CO2 over calcium carbonate at 1000K
CaCO3(s) <==> CaO(s) + CO2(g)
Kp = pCO2 * [CaO]/[CaCO3] = pCO2 ....( it is conventional to take the concentration (activity) of pure solid phases (e.g., CaCO3, CaO) to be equal to 1)
To do the calculations we need the thermodynamic values(dH, dG, dS etc) of the reactant and the products. You have not given the values. In that case we can use the standard table of thermodynamic values (at 25oC) and calculate the KP value at 25oC and derive the same at 1000K using the following equation:
ln (K2/K1) = dH0 [T2-T1/T1T2].......(where dH0 is assumed to be constant over the temperature range)
From the standard thermodynamic table we get,
dH° for the reaction = 177.8 kJ/mol
dS° for the reaction = 160.5 J/Kmol
dGo for the reaction = 130.431 kJ/mol
WE know, dGo = -RT ln KP
At 25oC, 130.431*103 J/mol = - (8.314 J/K.mol)(298K) ln KP
KP = 1.37*10-23
Multiply this with standard P= 1 atm
PCO2 at 298 K = 1.37*10-23 atm
ln (K2/K1) = (dH0/R) [T2-T1/T1T2]
ln(K2/1.37*10-23) = [(177.8 *103 J/mol)/(8.314J/mol/K)] [ 1000-298/1000*298]
K2 = 0.1
PCO2 at 1000 K = 0.1 atm