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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

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.

A mixture of one part nitrogen and three parts hydrogen is heated, in the presence of a suitable catalyst, to a temperature of 500掳 C. What fraction of the nitrogen (atom for atom) is converted to ammonia, if the final total pressure is 400 atm? Pretend for simplicity that the gases behave ideally despite the very high pressure. The equilibrium constant at 500掳 C is 6.9 x 10-5. (Hint: You'l have to solve a quadratic equation.)

Effect of altitude on boiling water.

(a) Use the result of the previous problem and the data in Figure 5.11 to plot a graph of the vapor pressure of water between 50C and 100C. How well can you match the data at the two endpoints?

(b) Reading the graph backward, estimate the boiling temperature of water at each of the locations for which you determined the pressure in Problem 1.16. Explain why it takes longer to cook noodles when you're camping in the mountains.

(c) Show that the dependence of boiling temperature on altitude is very nearly (though not exactly) a linear function, and calculate the slope in degrees Celsius per thousand feet (or in degrees Celsius per kilometer).

In this problem you will derive approximate formulas for the shapes of the phase boundary curves in diagrams such as Figures 5.31 and 5.32, assuming that both phases behave as ideal mixtures. For definiteness, suppose that the phases are liquid and gas.

(a) Show that in an ideal mixture of A and B, the chemical potential of species A can be written A=A+kTln(1-x)where A is the chemical potential of pure A (at the same temperature and pressure) and x=NB/NA+NB. Derive a similar formula for the chemical potential of species B. Note that both formulas can be written for either the liquid phase or the gas phase.

(b) At any given temperature T, let x1 and xgbe the compositions of the liquid and gas phases that are in equilibrium with each other. By setting the appropriate chemical potentials equal to each other, show that x1and xg obey the equations =1-xl1-xg=eGA/RTandxlxg=eGB/RT and where Grepresents the change in G for the pure substance undergoing the phase change at temperature T.

(c) Over a limited range of temperatures, we can often assume that the main temperature dependence of G=H-TScomes from the explicit T; both HandSare approximately constant. With this simplification, rewrite the results of part (b) entirely in terms of HA,HB TA, and TB (eliminating GandS). Solve for x1and xgas functions of T.

(d) Plot your results for the nitrogen-oxygen system. The latent heats of the pure substances areHN2=5570J/molandHO2=6820J/mol. Compare to the experimental diagram, Figure 5.31.

(e) Show that you can account for the shape of Figure 5.32 with suitably chosenH values. What are those values?

Assume that the air you exhale is at 35掳C, with a relative humidity of 90%. This air immediately mixes with environmental air at 5掳C and unknown relative humidity; during the mixing, a variety of intermediate temperatures and water vapour percentages temporarily occur. If you are able to "see your breath" due to the formation of cloud droplets during this mixing, what can you conclude about the relative humidity of your environment? (Refer to the vapour pressure graph drawn in Problem 5.42.)

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