Physical Chemistry
Physical Chemistry
2nd Edition
ISBN: 9781133958437
Author: Ball, David W. (david Warren), BAER, Tomas
Publisher: Wadsworth Cengage Learning,
Question
Book Icon
Chapter 4, Problem 4.62E
Interpretation Introduction

(a)

Interpretation:

The equation for Gibbs energy of mixing of gases is to be derived.

Concept introduction:

The term entropy is used to represent the randomness in a system. When a system moves from an ordered arrangement to a less ordered arrangement, then the entropy of the system increases. The entropy of mixing of gases is shown below.

ΔmixS=Ri=1no.ofgasesnilnxi

Expert Solution
Check Mark

Answer to Problem 4.62E

The equation for Gibbs energy of mixing of gases has been derived as shown below.

Explanation of Solution

The Gibbs free energy of mixing of gases is shown below.

ΔmixG=RTi=1no of gasesnilnxi …(1)

Where,

R represents the gas constant.

T represents the temperature.

ni represents the number of moles of the ith gas.

xi represents the mole fraction of the ith gas.

The entropy of mixing of gases is shown below.

ΔmixS=Ri=1no.ofgasesnilnxi …(2)

The change in Gibbs energy of the system is mathematically shown below.

ΔG=ΔHTΔS …(3)

Where,

ΔH represents the change in enthalpy of the system.

ΔG represents the change in Gibbs energy.

T represents the temperature of the system.

ΔS represents the change in entropy of the system.

The equation (3) can be written for the mixing process as shown below.

ΔmixG=ΔmixHTΔmixS …(4)

Assume that ΔmixH=0.

Substitute the value of ΔmixH in the equation (4).

ΔmixG=0TΔmixS=TΔmixS

Substitute the value of ΔmixS from equation (2) in the equation (4).

ΔmixG=T(R i=1 no.ofgases n iln x i)=RTi=1no.ofgasesnilnxi

Therefore, the equation for Gibbs energy of mixing of gases has been derived.

Conclusion

The equation for Gibbs energy of mixing of gases has been derived.

Interpretation Introduction

(b)

Interpretation:

The statement that the process of mixing of gases is always spontaneous is to be verified by a demonstration that the Gibbs free energy of mixing is always less than zero for a mixture of gases.

Concept introduction:

The Gibbs free energy of the system represents the maximum amount of non-expansion work achieved by a thermodynamic system at isothermal and isobaric conditions. The change in Gibbs free energy is used to predict the spontaneity of the process. The Gibbs free energy of mixing of gases is given below.

ΔmixG=RTi=1no of gasesnilnxi

Expert Solution
Check Mark

Answer to Problem 4.62E

The mole fraction of gas is always less than one. The natural logarithm of a number that is less than one is always negative. Therefore, the value of change in Gibbs free energy for mixing of gas is always negative and the process is always spontaneous.

Explanation of Solution

The Gibbs free energy of mixing of gases is shown below.

ΔmixG=RTi=1no of gasesnilnxi …(1)

Where,

R represents the gas constant.

T represents the temperature.

ni represents the number of moles of the ith gas.

xi represents the mole fraction of the ith gas.

The Gibbs free energy of mixing of two gases A and B can be given as shown below.

ΔmixG=RT(nAlnxA+nBlnxB)

The mole fraction of both the gases is always less than one. The natural logarithm of a number that is less than one is always negative. The result of the addition of two negative values is also negative.

The right-hand side of the equation is negative for the mixing of gases.

ΔmixG=negative

Therefore, the negative value of change in Gibbs free energy indicates that the process of mixing of gases is spontaneous.

Conclusion

The mole fraction of gas is always less than one. The natural logarithm of a number that is less than one is always negative. Therefore, the value of change in Gibbs free energy for mixing of gas is always negative and the process is always spontaneous.

Interpretation Introduction

(c)

Interpretation:

The value of ΔmixG for mixing 1.0molNe, 2.0molHe, and 3.0molAr at 35.0°C is to be calculated.

Concept introduction:

The Gibbs free energy of the system represents the maximum amount of non-expansion work achieved by a thermodynamic system at isothermal and isobaric conditions. The change in Gibbs free energy is used to predict the spontaneity of the process. The Gibbs free energy of mixing of gases is shown below.

ΔmixG=RTi=1no of gasesnilnxi

Expert Solution
Check Mark

Answer to Problem 4.62E

The value of ΔmixG for mixing 1.0molNe, 2.0molHe, and 3.0molAr at 35.0°C is 15538.400J.

Explanation of Solution

The number of moles of neon gas is 1.0mol.

The number of moles of helium gas is 2.0mol.

The number of moles of argon gas is 3.0mol.

The temperature of mixing is 35.0°C.

The temperature of mixing in Kelvin is shown below.

T=(273+35.0°C)K=308K

The total number of moles of gases is calculated as,

nt=nNe+nHe+nAr

Where,

nNe represents the number of moles of neon gas.

nHe represents the number of moles of helium gas.

nAr represents the number of moles of argon gas.

Substitute the value of nNe, nHe, and nAr in the above equation.

nt=1.0mol+2.0mol+3.0mol=6.0mol

The mole fraction of a substance present in a system is shown below.

xa=nant …(5)

Where,

na represents the number of moles of a substance ‘a’.

nt represents the total number of moles.

Substitute the value of the number of moles of neon gas and nt in the equation (5).

xNe=1.0mol6.0mol=0.1667

Substitute the value of the number of moles of helium gas and nt in the equation (5).

xHe=2.0mol6.0mol=0.3333

Substitute the value of the number of moles of argon gas and nt in the equation (5).

xAr=3.0mol6.0mol=0.50

The Gibbs free energy of mixing of gases is given as shown below.

ΔmixG=RT(nNelnxNe+nHelnxHe+nArlnxAr) …(6)

Where,

xNe represents the mole fraction of neon gas.

xHe represents the mole fraction of helium gas.

xAr represents the mole fraction of argon gas.

R represents the gas constant with a value of 8.314J/molK.

Substitute the value of R, temperature, number of moles and mole fractions of gases in the equation (6).

ΔmixG=(8.314J/molK)(308K)((1.0mol)ln(0.1667)+(2.0mol)ln(0.3333)+(3.0mol)ln(0.50))=(8.314J/molK)(308K)(6.068mol)=15538.400J

Therefore, the value of ΔmixG for mixing 1.0molNe, 2.0molHe, and 3.0molAr at 35.0°C is 15538.400J.

Conclusion

The value of ΔmixG for mixing 1.0molNe, 2.0molHe, and 3.0molAr at 35.0°C is 15538.400J.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
The change in Gibbs energy that accompanies the combustion of C6H12O6(s) to carbon dioxide and water vapour at 25 °c is -2828 kJ mol-1. The potential energy of an object of mass m at a height h, relative to that at the Earth's surface is given by mgh, where g = 9.81 m s-2 is the acceleration of freefall. How much glucose does a person of mass 65 kg need to consume to climb through 10m?
Calculate the change in molar Gibbs energy of carbon dioxide (treated as a perfect gas) at 20 °c when its pressure is changed isothermally from 1.0 bar to (a) 3.0 bar. (b) 2. 7 x 10-4 atm, its partial pressure in dry air at sea level.
Use the fundamental equation of therodynamics here tocalculate the change Gibbs energy when 3.1 mmol N_2(g) occupying 3.0L at 350 K expandsisothermally to 15 L.

Chapter 4 Solutions

Physical Chemistry

Ch. 4 - Consider a piston whose compression ratio is 10:1;...Ch. 4 - When one dives, water pressure increases by 1atm...Ch. 4 - Calculate G(25C) for this chemical reaction, which...Ch. 4 - Thermodynamic properties can also be determined...Ch. 4 - Calculate G in two different ways for the...Ch. 4 - Calculate G in two different ways for the...Ch. 4 - For the reaction C(graphite)C(diamond) at 25C,...Ch. 4 - Determine G for the following reaction at 0C and...Ch. 4 - What is the maximum amount of electrical that is,...Ch. 4 - When a person performs work, it is non-pV work....Ch. 4 - Can non-pV work be obtained from a process for...Ch. 4 - Can pV work be obtained from a process for which...Ch. 4 - Batteries are chemical systems that can be used to...Ch. 4 - The value of G for any phase change at constant p...Ch. 4 - The value of G for any phase change at constant p...Ch. 4 - Under what conditions is A=0 for a phase change?...Ch. 4 - Example 4.2 calculated A for one step of a Carnot...Ch. 4 - Can CV and Cp be easily defined using the natural...Ch. 4 - Analogous to equation 4.26, what is the expression...Ch. 4 - Prob. 4.30ECh. 4 - Prob. 4.31ECh. 4 - Prob. 4.32ECh. 4 - Although ideally, U=H=0 for a gas-phase process at...Ch. 4 - Use equations 4.21 and 4.25 to explain why H and G...Ch. 4 - Prob. 4.35ECh. 4 - Which of the following functions are exact...Ch. 4 - Prob. 4.37ECh. 4 - Prob. 4.38ECh. 4 - Prob. 4.39ECh. 4 - Equation 4.19 says that (UV)S=p If we are...Ch. 4 - For an isentropic process, what is the approximate...Ch. 4 - Use the ideal gas law to demonstrate the cyclic...Ch. 4 - Prob. 4.43ECh. 4 - Prob. 4.44ECh. 4 - Evaluate (U/V)T for an ideal gas. Use the...Ch. 4 - Evaluate (U/V)T for a van der Waals gas. Use the...Ch. 4 - Repeat the previous exercise for a gas that...Ch. 4 - Determine an expression for (p/S)T for an ideal...Ch. 4 - Determine the value of the derivative {[(G)]/T}p...Ch. 4 - Prob. 4.50ECh. 4 - Prob. 4.51ECh. 4 - A 0.988-mole sample of argon expands from 25.0L to...Ch. 4 - A 3.66-mol sample of He contracts from 15.5L to...Ch. 4 - Prob. 4.54ECh. 4 - Prob. 4.55ECh. 4 - Use the Gibbs-Helmholtz equation to demonstrate...Ch. 4 - For the equation 2H2(g)+O2(g)2H2O(g)...Ch. 4 - Use equation 4.46 as an example and find an...Ch. 4 - What is the value of G when 1.00mol of water at...Ch. 4 - Prob. 4.60ECh. 4 - Prob. 4.61ECh. 4 - Prob. 4.62ECh. 4 - Prob. 4.63ECh. 4 - Prob. 4.64ECh. 4 - What is the change in the chemical potential of a...Ch. 4 - Prob. 4.66ECh. 4 - Prob. 4.67ECh. 4 - Prob. 4.68ECh. 4 - Prob. 4.69ECh. 4 - Can equation 4.62 be used to calculate for an...Ch. 4 - Prob. 4.71ECh. 4 - Of helium and oxygen gases, which one do you...Ch. 4 - Prob. 4.73ECh. 4 - Use equation 4.39 to determine a numerical value...Ch. 4 - Prob. 4.75ECh. 4 - Prob. 4.76E
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY