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Use the data at the back of this book to calculate the slope of the calcite-aragonite phase boundary (at 298 K). You located one point on this phase boundary in Problem 5.28; use this information to sketch the phase diagram of calcium carbonate.

Short Answer

Expert verified

The calcium carbonate phase diagram would be linear up to temperature 58.2 SK, but as the temperature decreased, the pressure would not fall linearly, resulting in a non linear graph

Step by step solution

01

Given information

The slope of the phase boundary at T= 298K and P=3.597kBar is as follows:

dPdT=Sc-SaVc-Va……(1)

Where,

P is pressure

T is the temperature

V is the volume

Sc is the entropy of calcite

Sa is the entropy of aragonite

Vcis the volume of calcite

Va is the volume of aragonite

02

Calculations

From the book, we know that

Sc=92.9J/K,Sa=88.7J/K,Va=34.15cm3,Vc=36.93cm3

Substituting these values in equation 1

role="math" localid="1646902780078" dPdT=92.9J/K-88.7J/K36.93cm31m100cm3-34.15cm31m100cm3=1.51×106Pa/K10-5bar/K1Pa/K=15.1bar/K

Imagine the phase boundary is a straight line at T = 298K. The value of pressure at temperature T= 298K is P=3.6x 103 bar, which is well-known.

As a result, at critical temperature, the pressure differential can be represented as;

P(T)-P(298K)=dPdT(T-298K)

P(T) is the pressure at any given temperature T

Therefore, substituting the values

role="math" localid="1646903188657" P(T)=P(298)+dPdT(T-298)P(T)=3.597×103bar+15.1bar/K(T-298)

03

Explanation

So that the relationship between pressure and temperature is not linear, there must be a point when the change in pressure is zero, such that

0=3.6×103bar+15.1bar/K(T-298)(T-298K)=-3.6×103bar15.1bar/KT=298K-3.6×103bar15.1bar/KT=59.6K

The graph will not be linear at temperature T= 59.6K

04

Explanation

To build the graph, first get the different pressure values at various temperatures, then use the pressure and temperature values to draw the pressure vs temperature graph for the calcium carbonate phase diagram.

The calcium carbonate phase diagram would be linear up to temperature 58.2 SK, but as the temperature decreased, the pressure would not fall linearly, resulting in a non linear graph.

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Most popular questions from this chapter

Consider again the aluminosilicate system treated in Problem 5.29. Calculate the slopes of all three phase boundaries for this system: kyanite andalusite, kyanite-sillimanite, and andalusite-sillimanite. Sketch the phase diagram, and calculate the temperature and pressure of the triple point.

Consider a completely miscible two-component system whose overall composition is x, at a temperature where liquid and gas phases coexist. The composition of the gas phase at this temperature is xaand the composition of the liquid phase is xb. Prove the lever rule, which says that the proportion of liquid to gas is x-xa/xb-x. Interpret this rule graphically on a phase diagram.

A formula analogous to that for CP-CVrelates the isothermal and isentropic compressibilities of a material:

κT=κS+TVβ2CP.

(Here κS=-(1/V)(∂V/∂P)Sis the reciprocal of the adiabatic bulk modulus considered in Problem 1.39.) Derive this formula. Also check that it is true for an ideal gas.

Compare expression 5.68 for the Gibbs free energy of a dilute solution to expression 5.61 for the Gibbs free energy of an ideal mixture. Under what circumstances should these two expressions agree? Show that they do agree under these circumstances, and identify the function f(T, P) in this case.

The formula for Cp-Cv derived in the previous problem can also be derived starting with the definitions of these quantities in terms of U and H. Do so. Most of the derivation is very similar, but at one point you need to use the relation P=-(∂F/∂V)T.

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