An ideal diatomic gas, in a cylinder with a movable piston, undergoes the rectangular cyclic process shown in the given figure.

Assume that the temperature is always such that rotational degrees of freedom are active, but vibrational modes are "frozen out." Also assume that the only type of work done on the gas is quasistatic compression-expansion work.

(a) For each of the four steps A through D, compute the work done on the gas, the heat added to the gas, and the change in the energy content of the gas. Express all answers in terms of P1,P2,V1,andV2. (Hint: Compute ΔUbefore Q, using the ideal gas law and the equipartition theorem.)

(b) Describe in words what is physically being done during each of the four steps; for example, during step A, heat is added to the gas (from an external flame or something) while the piston is held fixed.

(c) Compute the net work done on the gas, the net heat added to the gas, and the net change in the energy of the gas during the entire cycle. Are the results as you expected? Explain briefly.

Short Answer

Expert verified

a. Work done on side A, B, C, D are 0J,-P2V2-V1,P1V2-V1and0Jrespectively. Heat added to the gas on side A is role="math" localid="1650461819764" 52V1P2-P1,along B is 72P2V2-V1,along C is -72P1V2-V1,and alongside D is -52V2P2-P1.

b. Along the side A, no work is done but heat is added to the gas to increase the pressure. Along the side B, the gas expands but heat must be added to achieve this. Similarly, along the side C, no work is done, and the gas gives off heat. Along the side D, work must be done on the gas to compress it and during this process gas gives off heat.

c. Net work done on the gas is Wtotal=V2-V1P1-P2,net heat added to the gas is Qtotal=V2-V1P2-P1=-Wiotal,and net energy change in this process isΔUrotal=0.

Step by step solution

01

Given information

An ideal diatomic gas, in a cylinder with a movable piston, undergoes the rectangular cyclic process shown in the given figure.

02

Calculation

We know formula for work done when volume varies is : W=-ViVfPdV.(1)

Here, P is pressure of the gas, ViandVfare initial and final volume.

If a system contains N molecules, each with f degree of freedom and there are no other temperature dependent forms of energy then it total thermal energy is

Urhermal=N·f·12kT..(2)

Technically it is just the average total thermal energy. But if N is large then the fluctuation away from average will be negligible.

First law of thermodynamics can be expressed as :Q=ΔU-W.(3)

Here, Q is amount of heat added, ΔUis net change in thermal energy and W is work done on gas.

The gas in this case is diatomic but the temperature is low enough that only translation (f=3) and rotational (f=2) degrees of freedom are excited so vibration modes are frozen out.

Work done for side A (since volume is constant along the side A, dV=0) is :WA=0(4)

For part B, volume is constant throughout so work done is :

WB=V1V2P2dVWB=-P2V2-V1..(5)

Here, pressure is constant at this side and V2>V1.

03

Step 3  : Calculation

On the other hand, work done on side D where volume is constant is : WD=0.(6)

For side C, the equation for pressure is :

WC=-P1V1-V2=P1V2-V1(7)WC=P1V2-V1

Thermal energy of the gas is U=52NkT=52PV

Along the side A, because the volume is constant, thermal energy is

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Most popular questions from this chapter

Two identical bubbles of gas form at the bottom of a lake, then rise to the surface. Because the pressure is much lower at the surface than at the bottom, both bubbles expand as they rise. However, bubble A rises very quickly, so that no heat is exchanged between it and the water. Meanwhile, bubble B rises slowly (impeded by a tangle of seaweed), so that it always remains in thermal equilibrium with the water (which has the same temperature everywhere). Which of the two bubbles is larger by the time they reach the surface? Explain your reasoning fully.

A frying pan is quickly heated on the stovetop 200CIt 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/gC).

Even at low density, real gases don’t quite obey the ideal gas law. A systematic way to account for deviations from ideal behavior is the virial

expansion,

PVnRT(1+B(T)(V/n)+C(T)(V/n)2+)

where the functions B(T), C(T), and so on are called the virial coefficients. When the density of the gas is fairly low, so that the volume per mole is large, each term in the series is much smaller than the one before. In many situations, it’s sufficient to omit the third term and concentrate on the second, whose coefficient B(T)is called the second virial coefficient (the first coefficient is 1). Here are some measured values of the second virial coefficient for nitrogen (N2):

T(K)
B(cm3/mol)
100–160
200–35
300–4.2
4009.0
50016.9
60021.3
  1. For each temperature in the table, compute the second term in the virial equation, B(T)/(V/n), for nitrogen at atmospheric pressure. Discuss the validity of the ideal gas law under these conditions.
  2. Think about the forces between molecules, and explain why we might expect B(T)to be negative at low temperatures but positive at high temperatures.
  3. Any proposed relation between P, V, andT, like the ideal gas law or the virial equation, is called an equation of state. Another famous equation of state, which is qualitatively accurate even for dense fluids, is the van der Waals equation,
    (P+an2V2)(Vnb)=nRT
    where a and b are constants that depend on the type of gas. Calculate the second and third virial coefficients (Band C) for a gas obeying the van der Waals equation, in terms of aand b. (Hint: The binomial expansion says that (1+x)p1+px+12p(p1)x2, provided that |px|1. Apply this approximation to the quantity [1(nb/V)]1.)
  4. Plot a graph of the van der Waals prediction for B(T), choosing aand bso as to approximately match the data given above for nitrogen. Discuss the accuracy of the van der Waals equation over this range of conditions. (The van der Waals equation is discussed much further in Section 5.3.)

Pretend that you live in the 19th century and don't know the value of Avogadro's number* (or of Boltzmann's constant or of the mass or size of any molecule). Show how you could make a rough estimate of Avogadro's number from a measurement of the thermal conductivity of gas, together with other measurements that are relatively easy.

Geologists measure conductive heat flow out of the earth by drilling holes (a few hundred meters deep) and measuring the temperature as a function of depth. Suppose that in a certain location the temperature increases by20Cper kilometer of depth and the thermal conductivity of the rock is 2.5W/mK. What is the rate of heat conduction per square meter in this location? Assuming that this value is typical of other locations over all of the earth's surface, at approximately what rate is the earth losing heat via conduction? (The radius of the earth is 6400km.)

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