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In Problem 1.16 you calculated the pressure of the earth’s atmosphere as a function of altitude, assuming constant temperature. Ordinarily, however, the temperature of the bottommost 10-15 km of the atmosphere (called the troposphere) decreases with increasing altitude, due to heating from the ground (which is warmed by sunlight). If the temperature gradient |dT/dz|exceeds a certain critical value, convection will occur: Warm, low-density air will rise, while cool, high-density air sinks. The decrease of pressure with altitude causes a rising air mass to expand adiabatically and thus to cool. The condition for convection to occur is that the rising air mass must remain warmer than the surrounding air despite this adiabatic cooling.

a. Show that when an ideal gas expands adiabatically, the temperature and pressure are related by the differential equation

dTdP=2f+2TP

b. Assume that dT/dzis just at the critical value for convection to begin so that the vertical forces on a convecting air mass are always approximately in balance. Use the result of Problem 1.16(b) to find a formula for dT/dzin this case. The result should be a constant, independent of temperature and pressure, which evaluates to approximately –10°C/km. This fundamental meteorological quantity is known as the dry adiabatic lapse rate.

Short Answer

Expert verified
  1. The required differential equation is dTdP=2f+2TP.
  2. The required expression is dTdz=−2mgkf+2.

Step by step solution

01

Part a. Step 1. Given.

The pressure of the earth’s atmosphere is a function of altitude with the temperature being constant. The temperature of the bottommost 10-15 km of the atmosphere decreases with increasing altitude due to heating from the ground.

If the temperature gradientdTdz exceeds a certain critical value then convection will occur.

02

Part a. Step 2. Formula used.

For adiabatic expansion, the relation between pressure, volume, and temperature is

PVγ=const. …… (1)

And

VTf2=const. …… (2)

Here,P is the pressure of the gas,V is the volume of the gas,T is the temperature in Kelvin,γ is the adiabatic exponent, andf is the degree of freedom γ=f+22.

03

Part a. Step 3. Calculation.

Isothermal compression is so slow that the temperature of the gas doesn’t rise at all and in adiabatic compression, the process is so fast that no heat escapes from the gas during the process. Most real compression processes will be somewhere between these extremes usually closer to the adiabatic approximation.

Differentiate equation (1) on both sides,

PVγ=const.

VγdP+γVγ−1PdV=0 …… (3)

Similarly, differentiate equation (2) on both sides,

Tf2dV+f2Tf2−1VdT=0 …… (4)

Divide equation (3) by Vγ−1on both sides

VγdP+γVγ−1PdVVγ−1=0VγdPVγ−1+γVγ−1Vγ−1PdV=0

VdP+γPdV=0 …… (5)

Divide equation (4) by Tf2−1on both sides

Tf2dV+f2Tf2−1VdTTf2−1=0Tf2dVTf2−1+f2Tf2−1Tf2−1VdT=0

TdV+f2VdT=0 …… (6)

Rearrange equation (5)

dP=−γPdVV …… (7)

Rearrange equation (6)

dT=−f2TdVV …… (8)

Divide equation (7) by equation (8)

dTdP=2fTdVV×VγPdV

dTdP=2fTγP …… (9)

Substitutef+2f forγ in equation (9)

dTdP=2f×ff+2TP

dTdP=2f+2TP.

04

Part a. Step 4. Conclusion.

Hence the required differential equation is dTdP=2f+2TP.

05

Part b. Step 1. Given.

Barometric equation is

dPdz=−mgkTP …… (1)

Here,m is mass,k is Boltzmann constant,T a²Ô»å P is temperature, and pressure respectively.

06

Part b. Step 2. Formula.

The relation between pressure, temperature, and volume is

dTdP=2f+2TP …… (2)

Here,f is the degree of freedom,T a²Ô»å P are temperature and pressure respectively.

07

Part b. Step 3. Calculation.

Isothermal compression is so slow that the temperature of the gas doesn’t rise at all and in adiabatic compression, the process is so fast that no heat escapes from the gas during the process. Most real compression processes will be somewhere between these extremes usually closer to the adiabatic approximation.

Simplify equation (1)

dPP=−mgkTdz …… (3)

From equation (2), it is found that

dT=2Tf+2dPP …… (4)

Substitute −mgkTdzfor dPPin equation (4)

dT=2Tf+2−mgkTdzdTdz=−2mgkf+2

08

Part b. Step 4. Conclusion.

Hence, the required expression is dTdz=−2mgkf+2.

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Most popular questions from this chapter

Put a few spoonfuls of water into a bottle with a tight lid. Make sure everything is at room temperature, measuring the temperature of the water with a thermometer to make sure. Now close the bottle and shake it as hard as you can for several minutes. When you're exhausted and ready to drop, shake it for several minutes more. Then measure the temperature again. Make a rough calculation of the expected temperature change, and compare.


For a solid, we also define the linear thermal expansion coefficient, α, as the fractional increase in length per degree:

α≡ΔL/LΔT
(a) For steel, α is 1.1 x 10-5 K-1. Estimate the total variation in length of a 1 km steel bridge between a cold winter night and a hot summer day.
(b) The dial thermometer in Figure 1.2 uses a coiled metal strip made of two different metals laminated together. Explain how this works.
(c) Prove that the volume thermal expansion coefficient of a solid is equal to the sum of its linear expansion coefficients in the three directions β=αx + αy + αz. (So for an isotropic solid, which expands the same in all directions, β =3 α .)


A frying pan is quickly heated on the stovetop 200∘CIt has an iron handle that is 20cmlong. Estimate how much time should pass before the end of the handle is too hot to grab with your bare hand. (Hint: The cross-sectional area of the handle doesn't matter. The density of iron is about7.9g/cm3and its specific heat is 0.45J/g⋅∘C).

Measured heat capacities of solids and liquids are almost always at constant pressure, not constant volume. To see why, estimate the pressure needed to keep Vfixed as Tincreases, as follows.

(a) First imagine slightly increasing the temperature of a material at constant pressure. Write the change in volume,dV1, in terms of dTand the thermal expansion coefficient βintroduced in Problem 1.7.

(b) Now imagine slightly compressing the material, holding its temperature fixed. Write the change in volume for this process, dV2, in terms of dPand the isothermal compressibility κT, defined as

κT≡−1V∂V∂PT

(c) Finally, imagine that you compress the material just enough in part (b) to offset the expansion in part (a). Then the ratio of dPtodTis equal to (∂P/∂T)V, since there is no net change in volume. Express this partial derivative in terms of βandκT. Then express it more abstractly in terms of the partial derivatives used to define βandκT. For the second expression you should obtain

∂P∂TV=−(∂V/∂T)P(∂V/∂P)T

This result is actually a purely mathematical relation, true for any three quantities that are related in such a way that any two determine the third.

(d) Compute β,κT,and(∂P/∂T)Vfor an ideal gas, and check that the three expressions satisfy the identity you found in part (c).

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Given the choice, would you rather measure the heat capacities of these substances at constant vor at constant p?

Suppose you open a bottle of perfume at one end of a room. Very roughly, how much time would pass before a person at the other end of the room could smell the perfume, if diffusion were the only transport mechanism? Do you think diffusion is the dominant transport mechanism in this situation?

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