One of the steps in the extraction of iron from its ore is the reduction of ironII oxode by CO at 900 degrees celsius FEO(s)+CO(g)--><-- Fe(s)+CO2(g)
IF CO is allowed to react with an excess of FEO, calculate the mole fractions of CO and CO2 at equilibrium . State any assumptions
i'll be giving a medal :)))
do you have any other info? like the eq. constant?
so at the equilibrium we establish that dG(T)=0... so the chemical equilibrium would be \[DeltaG ^{o}=-RTln K\] that in this case K=[CO2]/[CO] (as the activities of solids are equal to )
also the amount of moles that will react in CO will be equal to the moles of CO2... we will establish:\[DeltaG ^{o}=-RTln \left(\begin{matrix}\frac{ X }{ 1-X} \end{matrix}\right)\] 1 because we're gonna assume an initial mole fraction of 1 for CO
so, you need to calculate dG by hess' law... substitute and thats it
No, you need to get dG by Hess' law, and then get it at the given temperature the formula for getting the dG at (1173 K) would be:\[\frac{ dG ^{o}_{T} }{ T }=\frac{ dG ^{o}_{298} }{ 298 }-\int\limits_{298}^{T}\frac{ dH ^{o}_{T} }{ T ^{2} }\]
mmm you would also need\[dH ^{o}_{T}=dH ^{o}_{298}+\int\limits_{298}^{T}\Delta(nCp)dT\]
in case your Cp is variable (you'd also use Hess' law here), integrate and dont substitute the T value... just use it in the dG equation and the integrate again
@martaamador62 all clear?
@emilykrucker yes thanks for helping me :)
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