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

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

An ideal diatomic gas, in a cylinder with a movable piston, undergoes the rectangular cyclic process shown in Figure 1.10(b). 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.

  1. 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, and V2. (Hint: Compute role="math" localid="1651641251162" ΔUbefore Q, using the ideal gas law and the equipartition theorem.)
  2. 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.
  3. 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.

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

κT1VVPT

(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

PTV=(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).

(e) For water at 25C,β=2.57×104K1andκT=4.52×1010Pa1. Suppose you increase the temperature of some water from 20Cto30C. How much pressure must you apply to prevent it from expanding? Repeat the calculation for mercury, for which (at25C)β=1.81×104K1andκT=4.04×1011Pa1

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

The Fahrenheit temperature scale is defined so that ice melts at 320 F and water boils at 2120 F.

(a) Derive the formula for converting from Fahrenheit to Celsius and back

(b) What is absolute zero on the Fahrenheit scale?

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.)

Consider the combustion of one mole of methane gas:

CH4(gas)+2O2(gas)CO2(gas)+2H2O(gas)

The system is at standard temperature (298K)and pressure 105Paboth before and after the reaction.

(a) First imagine the process of converting a mole of methane into its elemental constituents (graphite and hydrogen gas). Use the data at the back of this book to find ΔHfor this process.

(b) Now imagine forming a mole of CO2and two moles of water vapor from their elemental constituents. Determine ΔHfor this process.

(c) What is ΔHfor the actual reaction in which methane and oxygen form carbon dioxide and water vapor directly? Explain.

(d) How much heat is given off during this reaction, assuming that no "other" forms of work are done?

(e) What is the change in the system's energy during this reaction? How would your answer differ if theH2Oended up as liquid water instead of vapor?

(f) The sun has a mass of2×1030kgand gives off energy at a rate of 3.9×1026watts. If the source of the sun's energy were ordinary combustion of a chemical fuel such as methane, about how long could it last?

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