Physics 4C Chapter 19: The Kinetic Theory of Gases

Similar documents
Unit 05 Kinetic Theory of Gases

Ch. 19: The Kinetic Theory of Gases

Chapter 15 Thermal Properties of Matter

The first law of thermodynamics continued

Chapter 19: The Kinetic Theory of Gases Questions and Example Problems

Chapter 19 The First Law of Thermodynamics

The Kinetic Theory of Gases

Physics 2 week 7. Chapter 3 The Kinetic Theory of Gases

Example problems. Chapter 3: The Kinetic Theory of Gases. Homework: 13, 18, 20, 23, 25, 27 (p )

Speed Distribution at CONSTANT Temperature is given by the Maxwell Boltzmann Speed Distribution

Heat and Thermodynamics. February. 2, Solution of Recitation 2. Consider the first case when air is allowed to expand isothermally.

Chapter 11. Molecular Composition of Gases

19-9 Adiabatic Expansion of an Ideal Gas

Speed Distribution at CONSTANT Temperature is given by the Maxwell Boltzmann Speed Distribution

Handout 11: Ideal gas, internal energy, work and heat. Ideal gas law

Chapter 18 Thermal Properties of Matter

Lecture 5. PHYC 161 Fall 2016

Physics Fall Mechanics, Thermodynamics, Waves, Fluids. Lecture 32: Heat and Work II. Slide 32-1

Temperature Thermal Expansion Ideal Gas Law Kinetic Theory Heat Heat Transfer Phase Changes Specific Heat Calorimetry Heat Engines

Handout 11: Ideal gas, internal energy, work and heat. Ideal gas law

Specific Heat of Diatomic Gases and. The Adiabatic Process

1. Each atom has a mass of m = M/N A, where M is the molar mass and N A is the Avogadro constant. The molar mass of arsenic is 74.9 g/mol or 74.

UNIVERSITY OF SOUTHAMPTON

Part I: Basic Concepts of Thermodynamics

(2) The volume of molecules is negligible in comparison to the volume of gas. (3) Molecules of a gas moves randomly in all direction.

6) BTW: Your TA has Exam3. It should have been returned to you on Nov 16 (Mon) at Recitation if you

Chapter 3 - First Law of Thermodynamics

Chapter 14 Kinetic Theory

Homework: 13, 14, 18, 20, 24 (p )

, is placed in thermal contact with object B, with mass m, specific heat c B. and initially at temperature T B

Phase Changes and Latent Heat

7. (2) Of these elements, which has the greatest number of atoms in a mole? a. hydrogen (H) b. oxygen (O) c. iron (Fe) d. gold (Au) e. all tie.

Physics 231 Topic 12: Temperature, Thermal Expansion, and Ideal Gases Alex Brown Nov

Conservation of Energy

CHAPTER 16 A MACROSCOPIC DESCRIPTION OF MATTER

Problem: Calculate the entropy change that results from mixing 54.0 g of water at 280 K with 27.0 g of water at 360 K in a vessel whose walls are

Videos 1. Crash course Partial pressures: YuWy6fYEaX9mQQ8oGr 2. Crash couse Effusion/Diffusion:

Chapter 14. The Ideal Gas Law and Kinetic Theory

ε tran ε tran = nrt = 2 3 N ε tran = 2 3 nn A ε tran nn A nr ε tran = 2 N A i.e. T = R ε tran = 2

Lecture 25 Thermodynamics, Heat and Temp (cont.)

6. (6) Show all the steps of how to convert 50.0 F into its equivalent on the Kelvin scale.

Properties of Gases. Properties of Gases. Pressure. Three phases of matter. Definite shape and volume. solid. Definite volume, shape of container

UNIT 10.

Lecture 24. Ideal Gas Law and Kinetic Theory

Molar Specific Heat of Ideal Gases

Lecture 7: Kinetic Theory of Gases, Part 2. ! = mn v x

KINETIC THEORY. was the original mean square velocity of the gas. (d) will be different on the top wall and bottom wall of the vessel.

QuickCheck. Collisions between molecules. Collisions between molecules

Ideal Gas Behavior. NC State University

Downloaded from

Gases. T boil, K. 11 gaseous elements. Rare gases. He, Ne, Ar, Kr, Xe, Rn Diatomic gaseous elements H 2, N 2, O 2, F 2, Cl 2

Collisions between molecules

KINETIC THEORY OF GASES

CHAPTER 21 THE KINETIC THEORY OF GASES-PART? Wen-Bin Jian ( 簡紋濱 ) Department of Electrophysics National Chiao Tung University


Chapter 5. The Gas Laws

Lecture 25 Goals: Chapter 18 Understand the molecular basis for pressure and the idealgas

Gases: Their Properties & Behavior. Chapter 09 Slide 1

CHEM Thermodynamics. Work. There are two ways to change the internal energy of a system:

Gases and Kinetic Theory

Gases. Characteristics of Gases. Unlike liquids and solids, gases

Ideal Gases. 247 minutes. 205 marks. theonlinephysicstutor.com. facebook.com/theonlinephysicstutor. Name: Class: Date: Time: Marks: Comments:

C H E M 1 CHEM 101-GENERAL CHEMISTRY CHAPTER 5 GASES INSTR : FİLİZ ALSHANABLEH

UNIVERSITY OF SOUTHAMPTON

Gases. Measuring Temperature Fahrenheit ( o F): Exceptions to the Ideal Gas Law. Kinetic Molecular Theory

Comparison of Solids, Liquids, and Gases

First Law of Thermodynamics

Chapter 19 Thermal Properties of Matter. A PowerPoint Presentation by Paul E. Tippens, Professor of Physics Southern Polytechnic State University

Chapter 5. The Properties of Gases. Gases and Their Properties. Why Study Gases? Gas Pressure. some very common elements exist in a gaseous state

The First Law of Thermodynamics

Chemical Thermodynamics : Georg Duesberg

Ch. 12 Notes - GASES NOTE: Vocabulary terms are in boldface and underlined. Supporting details are in italics.

kpa = 760 mm Hg? mm Hg P = kpa

Properties of Gases. assume the volume and shape of their containers. most compressible of the states of matter

Chapter 21 Solutions

Process Nature of Process

The First Law of Thermodynamics

Chapter 19 Entropy Pearson Education, Inc. Slide 20-1

The goal of thermodynamics is to understand how heat can be converted to work. Not all the heat energy can be converted to mechanical energy

Gas Volumes and the Ideal Gas Law

General Physics I (aka PHYS 2013)

Thermal Properties of Matter (Microscopic models)

Web Resource: Ideal Gas Simulation. Kinetic Theory of Gases. Ideal Gas. Ideal Gas Assumptions

A thermodynamic system is taken from an initial state X along the path XYZX as shown in the PV-diagram.

Quiz C&J page 365 (top), Check Your Understanding #12: Consider an ob. A) a,b,c,d B) b,c,a,d C) a,c,b,d D) c,b,d,a E) b,a,c,d

Kinetic Theory continued

14 The IDEAL GAS LAW. and KINETIC THEORY Molecular Mass, The Mole, and Avogadro s Number. Atomic Masses

Simpo PDF Merge and Split Unregistered Version -

PHY214 Thermal & Kinetic Physics Duration: 2 hours 30 minutes

Gas Laws. Gas Properties. Gas Properties. Gas Properties Gases and the Kinetic Molecular Theory Pressure Gas Laws

Final Review Solutions

Chapter 14 Thermal Physics: A Microscopic View

The Kinetic Theory of Gases

Apparatus for Studying the Relationship Between Pressure and Volume of a Gas

Lecture 24. Ideal Gas Law and Kinetic Theory

Kinetic Theory continued

Substances that Exist as Gases

= mol NO 2 1 mol Cu Now we use the ideal gas law: atm V = mol L atm/mol K 304 K

PES 2130 Exam 1/page 1. PES Physics 3 Exam 1. Name: SOLUTIONS Score: / 100

Properties of Gases. 5 important gas properties:

Transcription:

Physics 4C Chapter 19: The Kinetic Theory of Gases Whether you think you can or think you can t, you re usually right. Henry Ford The only thing in life that is achieved without effort is failure. Source unknown "We are what we repeatedly do. Excellence, therefore, is not an act, but a habit. Aristotle Reading: pages 507-529 Outline: Avogadro s number ideal gases ideal gas law work done at constant volume, pressure, and temperature rms speed and translational KE mean free path distribution of molecular speeds average, rms, and most probable speeds molar specific heats internal energy molar specific heat at constant volume and pressure degrees of freedom (diatomic and polyatomic gases) adiabatic expansion free expansions review of four special processes isothermal, isobaric, isochoric, adiabatic Problem Solving Techniques You should know the relationships between the mass of a molecule, the mass of a mole of molecules, and the total mass of a collection of molecules. If a gas contains N molecules, each of mass m, the total mass is Nm. Since there are N A molecules in a mole, the gas contains N/N A moles. The molar mass M is the mass of N A molecules: M = N A m. If the gas contains n moles, its total mass is nm. Note that this is exactly the same as Nm. Many problems require you to use the ideal gas law pv = nrt to compute one of the quantities that appear in it. You should also know how to compute changes in one of the quantities for various processes. For a change in volume (and temperature) at constant pressure, p V = nr T; for a change in pressure (and temperature) at constant volume, V p = nr T; and for a change in

volume (and pressure) at constant temperature, p V = - V p. In each case, the amount of gas was assumed to remain constant. You should understand how to compute the work done by a gas during a given process. Use W = p dv. First, you will need to find the functional form of the dependence of the pressure p on the volume V for the process. The ideal gas law is often helpful here. Use p = nrt/v. If the temperature is constant, the integral can be evaluated immediately. If the temperature is not constant you need to know how it changes. You should know how the root-mean-square speed of molecules in a gas depends on the temperature: v 3RT rms =, where M is the molar mass. You should also know how the M 3 average translational kinetic energy depends on the temperature: Kave = RT / N A. The 2 translational kinetic energy per mole is 3 2 RT, the energy of n moles is 3 nrt, and the 2 translational kinetic energy for N molecules is 3 NRT / N 3 A = NkT. For monatomic molecules 2 2 the last two expressions give the internal energy. For diatomic and polyatomic molecules other terms, giving the rotational energy, must be added. Other problems deal with the mean free path. You should be able to solve problems involving the first law of thermodynamics: E int = Q - W. For some of these you need to know the specific heat or the molar specific heat. Remember that the change in the internal energy is given by E int = nc V T and the energy input as heat is given by Q = nc T, where C is the molar specific heat for the process. Some problems deal with ideal gases as they undergo adiabatic processes. Remember that the combination pv γ remains constant for such processes. Here γ is the ratio of the specific heats: γ = C p /C V. The ideal gas law is still valid and for some problems pv = nrt must be solved simultaneously with pv γ = constant. Mathematical Skills This chapter introduces some of the ideas of statistics, the most important of which are the average and root-mean-square of a collection of numbers. To find the average, add the numbers and divide the result by the number of terms in the sum. To find the root-mean-square, add the squares of the numbers, divide the sum by the number of terms, and take the square root of the result. The root-mean-square is the square root of the average of the squares of the numbers. For practice, suppose the speeds of five molecules are 350 m/s, 225 m/s, 432 m/s, 375 m/s, and 450 m/s. Find their average and root-mean-square speeds. Your answers should be v ave = 366 m/s and v rms = 375 m/s. Notice that the average and root-mean-square values are different. In fact, the root-mean-square speed is greater than the average speed.

Integrals of the Maxwell distribution function. This chapter contains several integrals that are difficult to evaluate using only a knowledge of introductory calculus. They are associated with the average and mean-square speed for molecules with a Maxwellian speed distribution. The average speed is given by and the mean-square speed is given by Most standard integral tables list the following integrals: and Here p is any positive number and a is any integer. a! is the factorial of a; that is,. (2a-1)!! is the product of all odd integers from 1 to 2a-1; that is,. We use the first integral when x to an even power multiplies the exponential in the integrand and the second when x to an odd power multiplies the exponential. To evaluate the integral for the average speed of a Maxwellian distribution, substitute v = x and M/2RT = p into the equation for v avg. You should obtain The integral is the same as the second integral taken from the tables, with a = 1. So To evaluate the integral for the mean-square speed of a Maxwellian distribution, make the same substitutions to obtain

The integral is the same as the first one taken from the tables, with a = 2. So Thus, the root-mean-square speed is. Questions and Example Problems from Chapter 19 Question 1 (a) Rank the four paths in the figure below according to the work done by the gas, greatest first. (b) Rank paths 1, 2, and 3 according to the change in the internal energy of the gas, most positive first and most negative last. Question 2 An ideal diatomic gas, with molecular rotation but not oscillation, loses energy as heat Q. Is the resulting decrease in the internal energy of the gas greater if the loss occurs in a constant-volume process or in a constant-pressure process? Question 3 A certain amount of energy is to be transferred as heat to 1 mol of a monatomic gas (a) at constant pressure and (b) at constant volume, and to 1 mol of a diatomic gas (c) at constant pressure and (d) at constant volume. The figure below shows four paths from an initial point to four final points on a p-v diagram. Which path goes with which process? (e) Are the molecules of the diatomic gas rotating?

Problem 1 A quantity of ideal gas at 10.0 C and 100 kpa occupies a volume of 2.50 m 3. (a) How many moles of the gas are present? (b) If the pressure is now raised to 300 kpa and the temperature is raised to 30.0 C, how much volume does the gas occupy? Assume no leaks. Problem 2 The best laboratory vacuum has a pressure of about 1.00 10-18 atm, or 1.01 10-13 Pa. How many gas molecules are there per cubic centimeter in such a vacuum at 293 K?

Problem 3 Air that initially occupies 0.140 m 3 at a gauge pressure of 103.0 kpa is expanded isothermally to a pressure of 101.3 kpa and then cooled at constant pressure until it reaches its initial volume. Compute the work done by the air. (Gauge pressure is the difference between the actual pressure and atmospheric pressure.) Problem 4 At what temperature do atoms of helium gas have the same rms speed as molecules of hydrogen gas at 20.0 o C? (The molar masses are given in Table 19-1).

Problem 5 At 20 C and 750 torr pressure, the mean free paths for argon gas (Ar) and nitrogen gas (N 2 ) are λ Ar = 9.9 10-6 cm and λ N2 = 27.5 10-6 cm. (a) Find the ratio of the effective diameter of argon to that of nitrogen. What is the mean free path of argon at (b) 20 C and 150 torr, and (c) -40 C and 750 torr? Problem 6 Twenty-two particles have speeds as follows (N i represents the number of particles that have speed v i ): N i 2 4 6 8 2 v i (cm/s) 1.0 2.0 3.0 4.0 5.0 (a) Compute their average speed v avg. (b) Compute their root-mean-square speed v rms. (c) Of the five speeds shown, which is the most probable speed v P?

Problem 7 One mole of an ideal gas undergoes an isothermal expansion. Find the energy added to the gas as heat in terms of the initial and final volumes and the temperature. (Hint: Use the first law of thermodynamics.) Problem 8 One mole of an ideal diatomic gas goes from a to c along the diagonal path in the figure below. During the transition, (a) what is the change in internal energy of the gas, and (b) how much energy is added to the gas as heat? (c) How much heat is required if the gas goes from a to c along the indirect path abc?

Problem 9 Suppose 12.0 g of oxygen (O 2 ) is heated at constant atmospheric pressure from 25.0 C to 125 C. (a) How many moles of oxygen are present? (See Table 19-1 for the molar mass.) (b) How much energy is transferred to the oxygen as heat? (The molecules rotate but do not oscillate.) (c) What fraction of the heat is used to raise the internal energy of the oxygen? Problem 10 When 1.0 mol of oxygen (O 2 ) gas is heated at constant pressure starting at 0 C, how much energy must be added to the gas as heat to double its volume? (The molecules rotate but do not oscillate.)

Problem 11 The volume of an ideal gas is adiabatically reduced from 200 L to 74.3 L. The initial pressure and temperature are 1.00 atm and 300 K. The final pressure is 4.00 atm. (a) Is the gas monatomic, diatomic, or polyatomic? (b) What is the final temperature? (c) How many moles are in the gas? Problem 12 The figure below shows two paths that may be taken by a gas from an initial point i to a final point f. Path 1 consists of an isothermal expansion (work is 50 J in magnitude), an adiabatic expansion (work is 40 J in magnitude), an isothermal compression (work is 30 J in magnitude), and then an adiabatic compression (work is 25 J in magnitude). What is the change in the internal energy of the gas if the gas goes from point i to point f along path 2?