In Problems 3.30 and 3.31 you calculated the entropies of diamond and graphite at 500 K. Use these values to predict the slope of the graphite- diamond phase boundary at 500 K, and compare to Figure 5.17. Why is the slope almost constant at still higher temperatures? Why is the slope zero at T = 0?

Short Answer

Expert verified

At T=0 K the slope will be zero.

Step by step solution

01

Given information

We have the information of entropies, so

Entropy of diamond at500KisSa=7·59J/KEntropy of diamond at500KisSg=12·33J/KMolar Volumes of diamond isVd=3·42cm3=3.42×10-6m3Molar Volumes of graphite isVg=6·30cm3=5·30×10-6m3

Now, the change in entropies and molar volume will be:

Change in entropiesΔS=Sg-Sd=12·33J/K-7·59J/K=4.74J/K

role="math" localid="1646931515944" ChangeinMolarvolumesΔV=Vg-Vd=5·30×10-6m3-3·42×10-6m3=1.88×10-6m3

02

Calculation

The slope of phase boundary will be:

dPdT=ΔSΔV=4.74J/K1·88×10-6m3=2·5213×106N/m2KdPdT=2·52×106PaK

The graphite-diamond phase boundary slope at 500 K is this.

03

Calculations

ΔS0at high temperatures because, according to the Dulong-Petits law, both heat capacities approach 3R at high temperatures.

ΔS0

AsT0, both entropies approaches zero, soΔS0

dPdT=ΔSΔV=0

At T=0 K the slope will be zero.

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Most popular questions from this chapter

Go through the arithmetic to verify that diamond becomes more stable than graphite at approximately 15 kbar.

Problem 5.58. In this problem you will model the mixing energy of a mixture in a relatively simple way, in order to relate the existence of a solubility gap to molecular behaviour. Consider a mixture of A and B molecules that is ideal in every way but one: The potential energy due to the interaction of neighbouring molecules depends upon whether the molecules are like or unlike. Let n be the average number of nearest neighbours of any given molecule (perhaps 6 or 8 or 10). Let n be the average potential energy associated with the interaction between neighbouring molecules that are the same (4-A or B-B), and let uAB be the potential energy associated with the interaction of a neighbouring unlike pair (4-B). There are no interactions beyond the range of the nearest neighbours; the values of μoandμABare independent of the amounts of A and B; and the entropy of mixing is the same as for an ideal solution.

(a) Show that when the system is unmixed, the total potential energy due to neighbor-neighbor interactions is 12Nnu0. (Hint: Be sure to count each neighbouring pair only once.)

(b) Find a formula for the total potential energy when the system is mixed, in terms of x, the fraction of B.

(c) Subtract the results of parts (a) and (b) to obtain the change in energy upon mixing. Simplify the result as much as possible; you should obtain an expression proportional to x(1-x). Sketch this function vs. x, for both possible signs of uAB-u0.

(d) Show that the slope of the mixing energy function is finite at both end- points, unlike the slope of the mixing entropy function.

(e) For the case uAB>u0, plot a graph of the Gibbs free energy of this system

vs. x at several temperatures. Discuss the implications.

(f) Find an expression for the maximum temperature at which this system has

a solubility gap.

(g) Make a very rough estimate of uAB-u0for a liquid mixture that has a

solubility gap below 100°C.

(h) Use a computer to plot the phase diagram (T vs. x) for this system.

Let the system be one mole of argon gas at room temperature and atmospheric pressure. Compute the total energy (kinetic only, neglecting atomic rest energies), entropy, enthalpy, Helmholtz free energy, and Gibbs free energy. Express all answers in SI units.

The partial-derivative relations derived in Problems 1.46,3.33, and 5.12, plus a bit more partial-derivative trickery, can be used to derive a completely general relation between CPandCV.

(a) With the heat capacity expressions from Problem 3.33 in mind, first considerSto be a function of TandV.Expand dSin terms of the partial derivatives (S/T)Vand (S/V)T. Note that one of these derivatives is related toCV

(b) To bring in CP, considerlocalid="1648430264419" Vto be a function ofTand P and expand dV in terms of partial derivatives in a similar way. Plug this expression for dV into the result of part (a), then set dP=0and note that you have derived a nontrivial expression for (S/T)P. This derivative is related to CP, so you now have a formula for the difference CP-CV

(c) Write the remaining partial derivatives in terms of measurable quantities using a Maxwell relation and the result of Problem 1.46. Your final result should be

CP=CV+TVβ2κT

(d) Check that this formula gives the correct value of CP-CVfor an ideal gas.

(e) Use this formula to argue that CPcannot be less than CV.

(f) Use the data in Problem 1.46 to evaluateCP-CVfor water and for mercury at room temperature. By what percentage do the two heat capacities differ?

(g) Figure 1.14 shows measured values of CPfor three elemental solids, compared to predicted values of CV. It turns out that a graph of βvs.T for a solid has same general appearance as a graph of heat capacity. Use this fact to explain why CPand CVagree at low temperatures but diverge in the way they do at higher temperatures.

Sketch qualitatively accurate graphs of Gvs.Tfor the three phases ofH2O(ice, water, and steam) at atmospheric pressure. Put all three graphs on the same set of axes, and label the temperatures0°Cand 100°C. How would the graphs differ at a pressure of0.001bar?

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