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Everything in this section so far has ignored the boundary between two phases, as if each molecule were unequivocally part of one phase or the other. In fact, the boundary is a kind of transition zone where molecules are in an environment that differs from both phases. Since the boundary zone is only a few molecules thick, its contribution to the total free energy of a system is very often negligible. One important exception, however, is the first tiny droplets or bubbles or grains that form as a material begins to undergo a phase transformation. The formation of these initial specks of a new phase is called nucleation. In this problem we will consider the nucleation of water droplets in a cloud. The surface forming the boundary between any two given phases generally has a fixed thickness, regardless of its area. The additional Gibbs free energy of this surface is therefore directly proportional to its area; the constant of proportionality is called the surface tension,

GboundaryA

ff you have a blob of liquid in equilibrium with its vapor and you wish to stretch it into a shape that has the same volume but more surface area, then u is the minimum work that you must perform, per unit of additional area, at fixed temperature and pressure. For water at 20C,=0.073J/m2

(a) Consider a spherical droplet of water containing N1 molecules, surrounded by N-N1molecules of water vapor. Neglecting surface tension for the moment, write down a formula for the total Gibbs free energy of this system in terms of N,N1, and the chemical potentials of the liquid and vapor. Rewrite N1in terms of V1, the volume per molecule in the liquid, and T, the radius of the droplet.

(b) Now add to your expression for Ga term to represent the surface tension, written in terms of Tand u.

(c) Sketch a qualitative graph of G vs. T for both signs of 碌g - 碌1, and discuss the implications. For which sign of g-1does there exist a nonzero equilibrium radius? Is this equilibrium stable?

(d) Let TCrepresent the critical equilibrium radius that you discussed qualitatively in part (c). Find an expression for TCin terms of g-. Then rewrite the difference of chemical potentials in terms of the relative humidity (see Problem 5.42), assuming that the vapor behaves as an ideal gas. (The relative humidity is defined in terms of equilibrium of a vapor with a flat surface, or with an infinitely large droplet.) Sketch a graph of the critical radius as a function of the relative humidity, including numbers. Discuss the implications. In particular, explain why it is unlikely that the clouds in our atmosphere would form by spontaneous aggregation of water molecules into droplets. (In fact, cloud droplets form around nuclei of dust particles and other foreign material, when the relative humidity is close to 100%.)

Short Answer

Expert verified

Result is:

(a). The formula for total Gibbs free energy of this system isG=4r33vll-g+Ng.

(b). The improved formula is G=4r33vll-g+Ng+4r2.

(c). The qualitative graph betweenGvs.Tis

(c)Gr=4rc2vll-g+8rc=0

(d)h=e2vl/kTrc

Step by step solution

01

part(a) Step 1: Given information

we have been given thatGextra=A

02

part(a) Step 2:Simplify

The gibbs energy is given by:

G=Nll+N-Nlg

the volume of droplet

Vr=4r33

vl=4r33NlNl=4r33vl

03

part(b) Step 1: Given information

we have been given that replaceAwith2r2

04

part(b) Step 2:Simplify

After solving we get,

G=4r33vll-g+Ng+4r2
05

part(c) Step 1: Given information

we have been given thatGl-gr3+r2

06

part(c) Step 2:Simplify

it is clear that

l>g,Gr3+r2+C

l<g,G-r3+r2+C

07

part(d) Step 1: Given information

we have been given thatGr=4rc2vll-g+8rc=0

08

part(d) Step 2:Simplify

The change in gibbs energy is:

dG=-SdT+VdP+dN

at constant temperatur and number

dG=VdP

hence,dg-l=vg-vldP

solve for h to get:

h=e2vl/kTrc

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Most popular questions from this chapter

By subtracting Nfrom 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),

U-TS-N.

(a) Derive the thermodynamic identity for , and the related formulas for the partial derivatives ofwith respect toT,V, and N

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

(c) Prove that=-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 21019per cubic meter. Calculate for 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.)

Consider the production of ammonia from nitrogen and hydrogen,

N2+3H22NH3

at 298 K and 1 bar. From the values of 螖H and S tabulated at the back of this book, compute 螖G for this reaction and check that it is consistent with the value given in the table.

Figure 5.35 (left) shows the free energy curves at one particular temperature for a two-component system that has three possible solid phases (crystal structures), one of essentially pure A, one of essentially pure B, and one of intermediate composition. Draw tangent lines to determine which phases are present at which values of x. To determine qualitatively what happens at other temperatures, you can simply shift the liquid free energy curve up or down (since the entropy of the liquid is larger than that of any solid). Do so, and construct a qualitative phase diagram for this system. You should find two eutectic points. Examples of systems with this behaviour include water + ethylene glycol and tin - magnesium.

As you can see from Figure5.20,5.20,the critical point is the unique point on the original van der Walls isotherms (before the Maxwell construction) where both the first and second derivatives ofPPwith respect toVV(at fixedTT) are zero. Use this fact to show that

Vc=3Nb, Pc =127ab2 and kTc=827ab

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 for a monatomic ideal gas.

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