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Functions encountered in physics are generally well enough behaved that their mixed partial derivatives do not depend on which derivative is taken first. Therefore, for instance,

∂∂V∂U∂S=∂∂S∂U∂V

where each ∂/∂Vis taken with Sfixed, each ∂/∂Sis taken with Vfixed, and Nis always held fixed. From the thermodynamic identity (forU) you can evaluate the partial derivatives in parentheses to obtain

∂T∂VS=-∂P∂SV

a nontrivial identity called a Maxwell relation. Go through the derivation of this relation step by step. Then derive an analogous Maxwell relation from each of the other three thermodynamic identities discussed in the text (for H,F,andG ). Hold N fixed in all the partial derivatives; other Maxwell relations can be derived by considering partial derivatives with respect to N, but after you've done four of them the novelty begins to wear off. For applications of these Maxwell relations, see the next four problems.

Short Answer

Expert verified

Maxwell relations are:

∂T∂VS=-∂P∂SV∂T∂PS=∂V∂SP∂T∂PS=∂P∂TV∂S∂PT=-∂V∂TP

Step by step solution

01

To find

Four Maxwell relations.

02

Keeping N as constant derive the given equation.

We have the thermodynamics identity:

dU=TdS-PdV+μdN

at constant volume and number of molecules (at which dN=0anddV=0)

we have:

T=∂U∂SV............(1)

and at constant entropy and number of molecules (at which dN=0anddS=0)

we have:

P=-∂U∂VS............(2)

In the given we have: role="math" localid="1648414830374" ∂∂V∂U∂S=∂∂S∂U∂V.......(3)

Now substitute equation (1) and (2) in (3)

∂T∂VS=-∂P∂SV

03

continuing derivation

We have following the enthalpy identity as:

dH=TdS+VdP+μdN

at constant pressure and number of molecules (at which dN=0anddP=0) we have:

role="math" localid="1648416938771" T=∂H∂SP.........(3)

again differentiate equation (3) w.r.t. P

∂T∂PS=∂H∂P∂S

Then at constant entropy and number of molecules (at which dN=0anddS=0) we have:

role="math" localid="1648416952292" V=∂H∂PS.........(4)

again differentiate equation (4) w.r.t. V

∂V∂SP=∂H∂P∂S

combine these two equations together to get the following result:

∂T∂PS=∂V∂SP

04

continuing derivation 

We have following the Helmholtz free energy is given by:

dF=-SdT-PdV+μdN

at constant pressure and number of molecules (at which dN=0anddP=0) we have:

role="math" localid="1648418905850" S=-∂F∂TP......(5)

again differentiate equation (5) w.r.t. V

∂S∂VT=-∂F∂V∂T

and at constant entropy and number of molecules (at which dN=0anddS=0) we have:

role="math" localid="1648418958034" P=-∂F∂VS......(6)

again differentiate equation (6) w.r.t. T

∂P∂TV=-∂F∂V∂T

combine these two equations together to get the following result:

∂T∂PS=∂P∂TV

05

continuing derivation 

We have following the Gibbs free energy is given by:

dG=-SdT+VdP+μdN

at constant pressure and number of molecules (at which dN=0anddP=0) we have:

role="math" localid="1648419302437" S=-∂G∂TP.......(7)

again differentiate the equation (7) w.r.t. P

∂S∂PT=-∂G∂P∂T

and at constant temperature and number of molecules (at which dN=0anddT=0) we have:

role="math" localid="1648419374743" V=∂G∂PS.......(8)

again differentiate equation (8) w.r.t. T

∂V∂TP=∂G∂P∂T

combine these two equations together to get the following result:

∂S∂PT=-∂V∂TP

06

Final answer

Maxwell relations are:

∂T∂VS=-∂P∂SV∂T∂PS=∂V∂SP∂T∂PS=∂P∂TV∂S∂PT=-∂V∂TP

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Most popular questions from this chapter

Use the data at the back of this book to verify the values of ΔH and ΔGquoted above for the lead-acid reaction 5.13.

At temp 298K and pressure 1 bar.

Functions encountered in physics are generally well enough behaved that their mixed partial derivatives do not depend on which derivative is taken first. Therefore, for instance,
∂∂V∂U∂S=∂∂S∂U∂V

where each ∂/∂Vis taken with S fixed, each∂/∂S is taken with V fixed, and N is always held fixed. From the thermodynamic identity (for U ) you can evaluate the partial derivatives in parentheses to obtain

∂T∂VS=-∂P∂SV

a nontrivial identity called a Maxwell relation. Go through the derivation of this relation step by step. Then derive an analogous Maxwell relation from each of the other three thermodynamic identities discussed in the text (for H, F, and G ). Hold N fixed in all the partial derivatives; other Maxwell relations can be derived by considering partial derivatives with respect to N, but after you've done four of them the novelty begins to wear off. For applications of these Maxwell relations, see the next four problems.


Express ∂ΔG°/∂Pin terms of the volumes of solutions of reactants and products, for a chemical reaction of dilute solutes. Plug in some reasonable numbers, to show that a pressure increase of 1 atm has only a negligible effect on the equilibrium constant.

Derive the thermodynamic identity for G (equation 5.23), and from it the three partial derivative relations 5.24.

The methods of this section can also be applied to reactions in which one set of solids converts to another. A geologically important example is the transformation of albite into jadeite + quartz:

NaAlSi3O8⟷NaAlSi2O6+SiO2

Use the data at the back of this book to determine the temperatures and pressures under which a combination of jadeite and quartz is more stable than albite. Sketch the phase diagram of this system. For simplicity, neglect the temperature and pressure dependence of both ∆S and ∆V.

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