In Problem 1.40 you calculated the atmospheric temperature gradient required for unsaturated air to spontaneously undergo convection. When a rising air mass becomes saturated, however, the condensing water droplets will give up energy, thus slowing the adiabatic cooling process.

(a) Use the first law of thermodynamics to show that, as condensation forms during adiabatic expansion, the temperature of an air mass changes by dT=27TPdP-27LnRdnw

where nw is the number of moles of water vapor present, L is the latent heat of vaporization per mole, and I've assumed f=7/5for air.

(b) Assuming that the air is always saturated during this process, the ratio nw/n is a known function of temperature and pressure. Carefully express dnw/dz in terms of dP/dzanddT/dz, and the vapor pressure PvT. Use the Clausius-Clapeyron relation to eliminate dP/dT.

(c) Combine the results of parts (a) and (b) to obtain a formula relating the temperature gradient, dT/dz, to the pressure gradient, dP/dz. Eliminate Figure 5.18. Cumulus clouds form when rising air expands adiabatically and cools to the dew point (Problem 5.44); the onset of condensation slows the cooling, increasing the tendency of the air to rise further (Problem 5.45). These clouds began to form in late morning, in a sky that was clear only an hour before the photo was taken. By mid-afternoon they had developed into thunderstorms. the latter using the "barometric equation" from Problem 1.16. You should finally obtain dTdz=-27MgR1+PvPLRT1+27PvPLRT2

where " width="9">

(d) Calculate the wet adiabatic lapse rate at atmospheric pressure (I bar) and 25°C, then at atmospheric pressure and 0°C. Explain why the results are different, and discuss their implications. What happens at higher altitudes, where the pressure is lower?

Short Answer

Expert verified

(a). By using the first law of thermodynamics, it is proved that condensation forms during adiabatic expansion.

(b). dnw/dzin terms of role="math" localid="1651002425237" dP/dzand dT/dzcan be expressed as nwP=PnPgP=-nPgP2.

(c). The formula relating the temperature gradient dT/dzand pressure gradient dP/dzis dTdz=-2Mg7R1+PgPLRT1+27PgPLRT2.

(d) The wet adiabatic lapse rate is17.755.

Step by step solution

01

Part(a) step 1:Given information

We have been given that dU=-PdV-Ldnw

02

Part(a) step 2: Simplify

The energy as a function of temperature of:

U=f2nRT

fis the number of degree of freedom

PVγ=K

dT=27TPdP-27LnRdnw

03

Part(b) step1: Given information

We have been given that nwn=PgP

04

Part(b) Step 2: simplify

We are getting this in the end:

dnwdz=nwPdPdz+nwTdTdz

The partial derivatives are:

nwP=PnPgP=-nPgP2

05

Part(c) Step 1: Given information

We have been given that dTdz=27TPdPdz-27LnRdnwdz

06

Part(c) Step 2: Simplify

By substituting the results

dTdz1+27LRPdPgdT=dPdz27TP+27LPgRP2

From the barometric equation:

dPdz=-MgPRT

Solve to get:

dTdz=-2Mg7R1+PgPLRT1+27PgPLRT2

07

Part(d) Step 1: Given information

We have been given that Pg=Ce-L/RT

08

Part(d) Step 2: Simplify

The ratio of vapour pressure

LRT=43.99×103J/mol(8.314J/mol·K)(298K)=17.755

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Below 0.3 K the slope of the °He solid-liquid phase boundary is negative (see Figure 5.13).

(a) Which phase, solid or liquid, is more dense? Which phase has more entropy (per mole)? Explain your reasoning carefully.

(b) Use the third law of thermodynamics to argue that the slope of the phase boundary must go to zero at T = 0. (Note that the *He solid-liquid phase boundary is essentially horizontal below 1 K.)

(c) Suppose that you compress liquid *He adiabatically until it becomes a solid. If the temperature just before the phase change is 0.1 K, will the temperature after the phase change be higher or lower? Explain your reasoning carefully.

How can diamond ever be more stable than graphite, when it has

less entropy? Explain how at high pressures the conversion of graphite to diamond

can increase the total entropy of the carbon plus its environment.

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.)

Use a Maxwell relation from the previous problem and the third law of thermodynamics to prove that the thermal expansion coefficient β(defined in Problem 1.7) must be zero at T=0.

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.

See all solutions

Recommended explanations on Physics Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free