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Download Ch. 15 - UCSB Physics
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Chapter 15 Temperature and Heat Mechanics vs. Thermodynamics • Mechanics: • obeys Newton’s Laws • key concepts: force kinetic energy static equilibrium • Thermodynamics: • will find new ‘laws’ • key concepts: temperature, heat internal energy thermal equilibrium Newton’s 2nd Law 2nd Law of Thermodynamics Temperature (T) • Temperature = a macroscopic quantity • (see later: T is related to KE of particles) • many properties of matter vary with T: (length, volume, pressure of confined gas) Temperature (T) • Human senses can be deceiving • On a cold day: iron railings feel colder than wooden fences, but both have the same T • How can we define T ? • Look for macroscopic changes in a system when heat is added to it Two Thermometers Add heat to (a) and (b). (a) liquid thermometer • liquid level rises • T is measured by L (b) constant volume gas thermometer • gas pressure p rises • T is measured by p Using Thermometers • put the bulb of (a) in contact with a body • wait until the value of L (i.e. T) settles out • the thermometer and the body have reached thermal equilibrium (they have the same T) • Consider thermal interactions of systems in (a). • red slab = thermal conductor (transmits interactions) • blue slab = thermal insulator (blocks interactions) Demonstration • Let A and C reach thermal equilibrium (TA=TC). • Let B and C reach thermal equilibrium (TB=TC). • Then are A and B in thermal equilibrium (TA=TB)? Demonstration • In (a), are A and B in thermal equilibrium? • Yes, but it’s not obvious! • It must be proved by experiment! Demonstration • Experimentally, consider going from (a) to (b): • Thermally couple A to B and thermally decouple C. • Experiments reveal no macroscopic changes in A, B! Demonstration • This suggests the Zeroth Law of Thermodynamics: • If C is in thermal equilibrium with both A and B, then A and B in thermal equilibrium with each other. Demonstration • This means: If two systems A and B are in thermal equilibrium, they must have the same temperature (TA=TB), and vice versa Demonstration Temperature Scales Temperature Scales • Three scales: Fahrenheit, Celsius, Kelvin • To define a temperature scale, we need one or more thermodynamic fixed points • fixed point = a convenient, reproducible thermodynamic environment Temperature Scales • Both Fahrenheit and Celsius scales are defined using two fixed points: • freezing point and boiling point of water • Kelvin scale defined using one fixed point: • ‘triple point’ of water (all three phases coexist: ice, liquid, vapor) Temperature Scales: Summary • Relations among temperature scales: • Fahrenheit temperature 9 TF TC 32 5 • Celsius temperature 5 TC (TF 32 ) 9 • Kelvin temperature TK TC 273.15 Temperature Scales: Kelvin vs. Celsius • triple point of water: • we measure TC, triple = 0.01oC • we define TK, triple = 273.16 K • (DT)K = (DT)C so the unit of DT is K or oC • the scales differ only by an offset, so: TK = TC +273.15 Kelvin Temperature Scale • Fixed point = triple point of water: TK, triple • p = pressure of ‘ideal’ (i.e. low density) gas (on a constant volume gas thermometer) (has value ptriple at TK, triple) • We define: T (in kelvins) (constant) p 273.16 K p T (in kelvins) p triple • At low density, see same graph for all gases • Extrapolate to p=0 (at T = absolute zero K) Demonstration Thermal Expansion Thermal Expansion DL a DT L0 • Empirical law for solids, valid for small DT • (simple case: all directions expand equally) For a > 0: • If DT > 0: DL > 0 , material expands • If DT < 0: DL < 0 , material compresses Thermal Expansion DL a DT L0 a = coefficient of linear expansion > 0 (almost always) • characterizes thermal properties of matter • varies with material (and range of T) • unit: 1/K, or 1/oC since (DT)K = (DT)C Thermal Expansion DL a DT L0 • Example: two different materials have different DL • They can be used to build a thermometer or a thermostat • Atomic explanation of thermal expansion! • Recall ‘spring’ model for diatomic molecule: • Van der Waals potential energy, U Demonstration Thermal Expansion • Similar for a solid made of many atoms • Each pair of atoms has a potential energy U • The asymmetry of U explains thermal linear expansion! Thermal Volume Expansion: Solids and Liquids DV b DT V0 • b = coefficient of volume expansion • varies with material (and range of T) • unit: 1/K, or 1/oC since (DT)K = (DT)C Thermal Volume Expansion: Solids DV b DT V0 3a DT • Find a simple relationship between linear and volume expansion coefficients: • b = 3a Thermal Expansion of Water DV 3a DT V0 • ‘unusual’ state: • a < 0 if 0o C < T < 4 o C • (it’s why lakes freeze from the top down) Thermal Stress • Thermal stress= stress required to counteract (balance) thermal expansion • Tensile thermal stress: F Ya DT A Announcements • Midterms: will probably be returned Monday • Homework 5: is returned at front • Homework Extra Credit: is on record (but not yet listed on classweb if it brings a score over the maximum) Temperature Scales: Kelvin vs. Celsius • triple point of water: • we measure TC, triple = 0.01oC • we define TK, triple = 273.16 K • (DT)K = (DT)C so the unit of DT is K or oC • the scales differ only by an offset, so: TK = TC +273.15 Heat and Heat Transfer Quantity of Heat (Q) • Heat = energy absorbed or lost by a body due to a temperature difference • Heat = energy ‘in transit’ • SI unit: J • other units: 1 cal = 4.186 J 1 kcal = ‘calorie’ on food labels Quantity of Heat (Q) • Q > 0: heat is absorbed by a body • Q < 0: heat leaves a body • (we will see several expressions for Q) Quantity of Heat (Q) • Conservation of energy (‘calorimetry’): • For an isolated system, the algebraic sum of all heat exchanges add to zero Q1 + Q2 + Q3 + ... = 0 Absorption of Heat Q mc DT • Q = heat energy required to change the temperature of material (mass m) by DT • c = ‘specific heat capacity’ of the material (treat as independent T) unit: J/(kg ·K) Absorption of Heat Q mc DT dQ mc dT 1 dQ c m dT • If Q and DT positive: heat absorbed by m • If Q and DT negative: heat leaves m Do Exercise 15-35 Phase Changes • ‘phase’ = state of matter = solid, liquid, vapor • energy is needed to change phase of matter • under a phase transition of matter: only its phase changes, not its temperature! Phase Changes in Water Solid-Liquid Phase Change: Q = ± mLf • ± mLf = heat needed for phase change • Lf = ‘(latent) heat of fusion’ of the material = (heat/unit mass) needed for transition unit: J/kg • + for melting (solid to liquid) – for freezing (liquid to solid) Do Exercise 15-51 Liquid-Vapor Phase Change: Q = ± mLv • ± mLv = heat needed for phase change • Lv = ‘(latent) heat of vaporization’ = (heat/unit mass) needed for transition unit: J/kg • + for evaporating (liquid to vapor) – for condensing (vapor to liquid) Heat Transfer Heat Transfer dQ/dt = rate of heat flow = ‘heat current’ Three mechanisms for achieving heat transfer: • Conduction • Convection • Radiation Heat Transfer Mechanisms • Conduction: Collisions of molecules, no bulk motion • Convection: Bulk motion from one region to another • Radiation: Emission of electromagnetic waves Conduction Conduction TH TC dQ H kA dt L • k = thermal conductivity of material unit: W/(m·K) • A = cross sectional area of material • L = length of material Do Exercises 15-57, 15-58 Notes on a composite conducting rod Conduction k thermal conductivi ty, unit : W/(m K) TH TC dQ H kA dt L Convection (usually complicated) Radiation (e.g. emitted by the sun) Radiation = Electromagnetic Waves Emission of Radiation dQ H AeT 4 dt 5.67 10-8 W/(m 2 K 4 ) • • • • all bodies emit electromagnetic radiation A = surface area of body T = surface temperature of body e = emissivity of body (0 < e < 1) Do Exercise 15-67 Example of net radiation and Problem 15-89 Absorption of Radiation • In general, bodies emit radiation and also absorb radiation from their surroundings • T = surface temperature of body • TS = surface temperature of surroundings H net AeT AeTS 4 Ae (T 4 TS ) 4 4