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Imagine some helium in a cylinder with an initial volume of 1 liter and an initial pressure of 1 atm. Somehow the helium is made to expand to a final volume of 3 liters, in such a way that its pressure rises in direct proportion to its volume.

  1. Sketch a graph of pressure vs. volume for this process.
  2. Calculate the work done on the gas during this process, assuming that there are no “other” types of work being done.
  3. Calculate the change in the helium’s energy content during this process.
  4. Calculate the amount of heat added to or removed from the helium during this process.
  5. Describe what you might do to cause the pressure to rise as the helium expands.

Short Answer

Expert verified
  1. The graph between pressure and volume is a straight line but does not pass through the origin.
  2. Work done on the gas is W=405.2 J.
  3. Change in helium’s energy is ΔU=1216.05 J.
  4. The amount of heat added is Q=1621.25 J.
  5. Pressure increases when kinetic energy increases. To increase pressure, kinetic should be increased and finally, it is concluded that one has to increase the temperature to increase pressure.

Step by step solution

01

Part a. Step 1. Introduction.

The pressure versus volume diagram can be drawn by taking pressure on y-axis and volume on x-axis. In this process, since the pressure is directly proportional to the volume so the final pressure vs. volume graph is a straight line but does not pass through the origin.

02

Part a. Step 2. Explanation.

Since the pressure is directly proportional to the volume of helium gas so for this process, the graph between pressure and volume is a straight line but does not pass through the origin. The required graph between pressure and volume is shown below:

03

Part a. Step 3. Conclusion.

Hence, the graph between pressure and volume is a straight line but does not pass through the origin.

04

Part b. Step 1. Given.

Initial volume isVi=1 liter

Final volume isVf=3 liter

Initial pressure isPi=1 atm

05

Part b. Step 2. Formula used.

Expression for work done on the system is

W=vivfPdV …… (1)

Here Pis the pressure, Vi and  Vfare initial volume, and final volume.

Pressure is directly proportional to the volume as given i.e.

PV …… (2)

P=VA …… (3)

Here Ais the proportionality constant.

06

Part b. Step 3. Calculation.

From equation (3) it can be simplified as for the initial and final case

PiVi=A …… (4)

And

PfVf=A …… (5)

From equations (4) and (5)

PiVi=PfVf

Pf=PiVfVi …… (6)

Substitute1×103forViand3×103forVfand1.013×105forPiin equation (6)

Pf=3×103×1.013×1051×103Pf=3.04×105 Pa

In the graph between pressure and volume, the slope is calculated as

A=PfPiVfVi …… (7)

Substitute 1×103forViand3×103for Vf,1.013×105forPiand3.04×105forPfin equation (7)

A=3.04×1051.013×1053×103103A=1.013×108 Pa.m-3

Hence the relation between pressure and volume is

P=1.013×108V ….. (8)

Substitute1.013×108VforPin equation (1)

W=vivf1.013×108V.dV …… (9)

Again substitute the upper and lower limit of the above integral i.e. 1×103for Viand 3×103for Vfin equation (9)

W=1033×1031.013×108V.dVW=1.013×1081033×103V.dVW=1.013×108V221033×103W=405.2 J

07

Part b. Step 4. Conclusion.

Hence, work done on the gas is W=405.2 J.

08

Part c. Step 1. Given.

Initial volume and final volume are1×103and3×103respectively and initial and final pressure are1.013×105and3.04×105respectively.

09

Part c. Step 2. Formula used.

Thermal energy can be expressed as

Uthermal=Nf12kT …… (10)

Here, fstands for the degree of freedom, Nstands for a number of molecules, kstands for Boltzmann constant, and Tstands for temperature in Kelvin.

The equation of ideal gas is

PV=NkT …… (11)

Here, Pis the pressure of the gas, Vis the volume of gas contained, kis Boltzmann constant, Tis the temperature in Kelvin and Nis the number of molecules.

10

Part c. Step 3. Calculation.

Equation (10) can be simplified as by substitutePVforNkT

Uthermal=f2PV …… (12)

Change in thermal energy due to expansion is

ΔU=PfVfPiVi …… (13)

Equation (12) can be written as a substitutePfVfPiVifor ΔU

ΔU=32ΔPV=32.PfVfPiVi …… (14)

Substitute 1×103for Viand 3×103for Vf,1.013×105forPiand3.04×105forPfin equation (14)

ΔU=323.04×105×3×1031.013×105×103ΔU=1216.05 J

11

Part c. Step 4. Conclusion.

Hence, a change in helium’s energy is ΔU=1216.05 J.

12

Part d. Step 1. Given.

Change in energy isΔU=1216.05 Jand work done is W=405.2 J.

13

Part d. Step 2. Formula used.

The equation for the first law of thermodynamics is
Q=ΔUW …… (15)

Where Qis the amount of heat added or removed, ΔUis a change in internal energy, Wand is external work done

14

Part d. Step 3. Calculation.

Substitute1216.05 JforΔUand405.2 JforWin equation (15)

Q=1216.05+405.2 J

Q=1621.25 J

Since the sign ofQis positive so heat is added to the system.

15

Part d. Step 4. Conclusion.

Hence, the amount of heat added is Q=1621.25 J.

16

Part e. Step 1. Introduction

The motion of a body is related to the change in kinetic energy of the body. The kinetic energy of the body is directly proportional to the change in temperature of the body.

17

Part e. Step 2. Explanation.

Kinetic energy is directly proportional to the temperature. Similarly, pressure is also directly proportional to kinetic energy. So, it can be concluded that pressure is also proportional to temperature. Basically, to increase pressure, one has to increase temperature.

18

Part e. Step 3. Conclusion.

Hence, to increase pressure, one has to increase the temperature.

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Most popular questions from this chapter

Estimate the average temperature of the air inside a hot-air balloon (see Figure 1.1). Assume that the total mass of the unfilled balloon and payload is 500 kg. What is the mass of the air inside the balloon?

Suppose you have a gas containing hydrogen molecules and oxygen molecules, in thermal equilibrium. Which molecule are moving faster, on average? By what factor?

Calculate the rms speed of a nitrogen molecule at a room temperature?

The Rankine temperature scale(abbreviated °R) uses the same scale size degrees as Fahrenheit, but measured up from absolute zero like Kelvin(so Rankine is to Fahrenheit as Kelvin is to Celsius). Find the conversion formula between Rankine and Fahrenheit and also between Rankine and Kelvin. What is the room temperature on the Rankine 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.)
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