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Show that equation 5.40 is in agreement with the explicit formula for the chemical potential of a monatomic ideal gas derived in Section 3.5. Show how to calculate μ°for a monatomic ideal gas.

Short Answer

Expert verified

Explicit formula for the chemical potential of a monoatomic ideal gas is

μ=-kTlnkTp02πmkTh23/2+kTlnpp0and the value ofμ0is-kTlnkTp02πmkTh23/2

Step by step solution

01

To determine

The explicit formula for a monoatomic ideal gas's chemical potential, as well as the value of ideal chemical potential.

02

Explanation for the solution

The chemical potential of the gas expression is given below.

μ=GNT,P

where

role="math" localid="1648236173152" μis the chemical potential,Gis the Gibbs energy andNis the number of gas molecules.

When more particles are added to a system while the temperature and pressure remain constant, the system's Gibbs energy increases by μ

Write the expression for chemical potential in terms of standard chemical potential at atmospheric pressure.

μ(T,P)=μ0(T)+kTlnP/P0(1)

Here, μ0(T)is the standard chemical potential, kis Boltzmann constant, Tis the absolute temperature and P0is the atmospheric pressure.

The ideal gas equation is

PV=NkT

Here, Pis the pressure of the gas,

Vis the volume,

kis Boltzmann constant and

Tis the absolute temperature.

03

Continuation for the solution

Now, the chemical potential of an ideal gas expression is given below:

μ=-kTlnVN2πmkTh23/2..(2)

Substitute(KTP)for(VN)in expression (2).

μ=-kTlnkTP2πmkTh23/2=-kTlnkTp0PP02πmkTh23/2=-kTlnkTp02πmkTh23/2-kTlnp0P

Simplify the above expression

μ=-kTlnkTp02πmkTh23/2+kTlnpp0..(3)

The equation (1) and (3) are similar to each other.

μ0=-kTlnkTp02πmkTh23/2

Substitute the above expression in (3)

μ=μ0+kTlnPp0

Therefore explicit formula for the chemical potential of a monoatomic ideal gas is

μ=-kTlnkTp02πmkTh23/2+kTlnpp0and the value ofu0is-kTlnkTp02πmkTh23/2

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Most popular questions from this chapter

Repeat the previous problem for the diagram in Figure 5.35 (right), which has an important qualitative difference. In this phase diagram, you should find that β and liquid are in equilibrium only at temperatures below the point where the liquid is in equilibrium with infinitesimal amounts of αandβ . This point is called a peritectic point. Examples of systems with this behaviour include water + NaCl and leucite + quartz.

By subtracting μNfrom localid="1648229964064" U,H,F,orG,one can obtain four new thermodynamic potentials. Of the four, the most useful is the grand free energy (or grand potential),

ΦU-TS-μN.

(a) Derive the thermodynamic identity for Φ, and the related formulas for the partial derivatives ofΦwith respect toT,V, and μN

(b) Prove that, for a system in thermal and diffusive equilibrium (with a reservoir that can supply both energy and particles), Φtends to decrease.

(c) Prove thatϕ=-PV.

(d) As a simple application, let the system be a single proton, which can be "occupied" either by a single electron (making a hydrogen atom, with energy -13.6eV) or by none (with energy zero). Neglect the excited states of the atom and the two spin states of the electron, so that both the occupied and unoccupied states of the proton have zero entropy. Suppose that this proton is in the atmosphere of the sun, a reservoir with a temperature of 5800Kand an electron concentration of about 2×1019per cubic meter. Calculate Φfor both the occupied and unoccupied states, to determine which is more stable under these conditions. To compute the chemical potential of the electrons, treat them as an ideal gas. At about what temperature would the occupied and unoccupied states be equally stable, for this value of the electron concentration? (As in Problem 5.20, the prediction for such a small system is only a probabilistic one.)

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.

In this problem you will investigate the behavior of a van der Waals fluid near the critical point. It is easiest to work in terms of reduced variables throughout.

(a) Expand the van der Waals equation in a Taylor series in , keeping terms through order . Argue that, for T sufficiently close to Tc, the term quadratic in (V-VC)becomes negligible compared to the others and may be dropped.

(b) The resulting expression for P(V) is antisymmetric about the point V = Ve. Use this fact to find an approximate formula for the vapor pressure as a function of temperature. (You may find it helpful to plot the isotherm.) Evaluate the slope of the phase boundary,dP/dT

( c) Still working in the same limit, find an expression for the difference in volume between the gas and liquid phases at the vapor pressure. You should find Vg-VlTc-Tβ.8, where (3 is known as a critical exponent. Experiments show that (3 has a universal value of about 1/3, but the van der Waals model predicts a larger value.

(d) Use the previous result to calculate the predicted latent heat of the transformation as a function of temperature, and sketch this function.

The shape of the T = Tc isotherm defines another critical exponent, called P-PcV-VcδCalculate 5 in the van der Waals model. (Experimental values of 5 are typically around 4 or 5.)

A third critical exponent describes the temperature dependence of the isothermal compressibility, K=-t This quantity diverges at the critical point, in proportion to a power of (T-Tc) that in principle could differ depending on whether one approaches the critical point from above or below. Therefore the critical exponents 'Y and -y' are defined by the relations

κT-Tc-γTc-T-γ'

Calculate K on both sides of the critical point in the van der Waals model, and show that 'Y = -y' in this model.

A muscle can be thought of as a fuel cell, producing work from the metabolism of glucose:

C6H12O6+6O26CO2+6H2O

(a) Use the data at the back of this book to determine the values of ΔHand ΔGfor this reaction, for one mole of glucose. Assume that the reaction takes place at room temperature and atmospheric pressure.

(b) What is maximum amount of work that a muscle can perform , for each mole of glucose consumed, assuming ideal operation?

(c) Still assuming ideal operation, how much heat is absorbed or expelled by the chemicals during the metabolism of a mole of glucose?

(d) Use the concept of entropy to explain why the heat flows in the direction it does?

(e) How would your answers to parts (a) and (b) change, if the operation of the muscle is not ideal?

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