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Chapter p 19 The first law of thermodynamics 19.1 Thermodynamic systems 19.2 Work done during g volume changes g 19.3 Paths between thermodynamic states 19 4 Internal energy and first law of 19.4 thermodynamics 19 5 Kinds of thermodynamic processes 19.5 19.6 Internal energy of an ideal gas 19 7 Heat capacities of an ideal gas 19.7 19.8 Adiabatic processes for an ideal gas Thermodynamics • The study of relationships involving heat, mechanical work, and other aspects of energy and energy transfer • Name few example of thermodynamics processes • First law of thermodynamics deals with conversion of energy in a thermodynamic system • Name an example of mechanical energy transfer • Name an example of heat transfer • First law will combine two forms of energy Thermodynamic systems • Thermodynamic systems: Any collection of objects that is convenient to regard as a unit unit, and that may have potential to exchange energy with its surroundings g • Thermodynamic processes: any process during which there are changes in the state of the thermodynamic system • State of a thermodynamic system is defined by its state variables such as T, P, V • Thermodynamics does not depend on details of the structure of matter so both microscopic and macroscopic treatment lead to the same result. Sign convention for exchange of energy between a thermodynamic system and environment Thermodynamics: work done by the system is + Mechanics: work done by the forces acting on the body is + Sign of work in thermodynamics and mechanics are opposite Sign of the work done during a volume change (whoever does the work has the positive W) Contraction: W(molecules)<0 Expansion: p W(molecules)>0 A Work done in a volume change F = pA A dW = Fdx = pAdx Adx = dV Ad dW = pdV W= V2 ∫ p(V )dV V1 Always V1 is initial state V2 is final If p is a variable (not a constant) we need to know its functionality with V to solve the integral. Work done in constant pressure: W = p (V2 − V1 ) Name an example of a PV relationship Calculating work using PV diagrams Work is the area under the curve that represents pressure change as a function of volume change W = ∑ pi ΔVi = Area under the pV curve i • Verify sign of the work during an expansion and contraction process with the convention set before Example: Isothermal expansion of an ideal gas • An ideal g gas undergoes g an isothermal (constant-temperature) expansion at T, during g which its volume changes g from V1 to V2. How much work does the gas do? • How much is the volume expansion of an ideal gas if the work is 2nRT? Paths between thermodynamic states: work • Calculate the work done by the system to get from P1V1 to P2V2 on the paths 132, 142,12. • Does D th the work kd depend d on th the path? th? Paths between thermodynamic states: heat Rapid removal of the wall and free expansion Gradual expansion and moving the piston up Q1 W1 Q2=0 W2=0 0 ΔT=0 • How much is the amount of the work done by the system in a and b for one mole of an ideal gas Stop and think • What do you think about “the the amount of work contained in a system”? Can it be defined clearly? • Can you name a system that the work done by it does not depend on the path? Internal energy and the first law of thermodynamics: a generalization of the conservation of energy • • • • Internal energ energy, U, U of a system s stem is ssum m of the kinetic energies of all of its constituents plus sum of the potential energy of the interaction among these particles. When heat added to a system, system its internal energy increases ΔU ΔU=Q Q When work is done by a system its internal energy decreases by the amount of work by ΔU=-W Total change in internal energy of a system is ΔU ΔU=Q-W QW How we determine the internal energy off a system? ? • We can’t determine absolute value of the internal energy of a system (similar to the potential energy). • We choose an state of a system as reference and give an arbitrary value to its internal energy. • Then we can measure change in internal energy using i th the h heatt exchange h and d work kd done b by/on / the system ΔU=Q-W e dQ a and dd dW bot both depe depend do on tthe e pat path,, itt • While turns out that ΔU does not depend on the path. ΔU only depends on the state of a system which is a function of its state variables (p (p, V V, T) Change in internal energy of human body in 24 hours Work done during a change of sate Summary Summary: The first law of thermodynamics h d i Summary: Internal energy Example • You intake 900 calorie and run up a cliff cliff. How high do you have to climb to burn all calories consumed? (your mass is 60 kg) (ans. 6410 m) • Evaluate your answer answer. A cyclic process • State of a system y starts and ends at a. The total work is 500 J. – Why is the work negative? – Find the change in internal energy and the heat added to the system in this process process. • For pV diagrams total work is positive for clockwise processes and negative for counterclockwise. Can you contradict it? Comparing thermodynamic processes Kinds of thermodynamic processes • • • • Adiabatic: no heat transfer Isobaric: constant pressure I Isochoric: h i constant t t volume l Isothermal: constant temperature Adiabatic processes and the first law • No heat transfer: Q=0 can be achieved in – Isolated systems – Fast processes • First Law: ΔU ΔU=-W W • In adiabatic expansion system does positive work and hence looses energy. W>0 and ΔU<0 • In I adiabatic di b ti compression i system t d does negative ti work k and hence gains energy. W<0 and ΔU>0 • Example: p compression p stroke in an internal combustion, expansion of the fuel during the power stoke (temperature rise or drop happens during the process) Isochoric processes and the first law • No change of volume: W=0 W 0 is zero • First Law: ΔU=Q; • All the energy added to the system remains in it and cusses temperature change • Example: heating gas in a cylinder (don’t (don t try it at home) • Although t oug tthere eea are e ot other e kinds ds o of work o tthat at do not involve volume change but “isochoric” is used for the systems that no work is done at all. Isobaric processes and the first law • No change of pressure: none of the ΔU, ΔU Q Q, or W is zero • First Law: ΔU=Q-W; ΔU=Q W; • Work is calculated easily W=p(V2-V1) Isothermal processes and the first law • No change of temperature: process has to occur slowly and none of the ΔU, Q, or W is zero • First Law: ΔU=Q-W; • In I special i l cases ΔT=0 ΔT 0 means ΔU=0 ΔU 0 (Example: ideal gas) but generally ΔU is nott zero. Thermodynamic processes on PV diagrams di Internal energy of an ideal gas • Example: adiabatic expansion of a gas If U depended on V or p then gas. we would have observed a change in T. • Experiment shows no change in T for expansion of low density gasses. • Internal I t l energy off an ideal id l gas depends only on its temperature, not on its pressure or volume. • For a non-ideal gas adiabatic expansion is accompanied with p in temperature. p drop • Does internal energy of a solid depend on its volume? Heat capacities of an ideal gas • Cp molar heat capacity p y under constant pressure (usually for gasses) • Cv molar l h heatt capacity it under constant volume (for solids or liquids) • For a given system (ideal gas) why these should be different? Which one is greater? Cp=Cv+R molar heat capacities of an ideal gas Usually Cv=.4Cp For water Cv<Cp between 0 and 40C More about heat capacities • Ratio of heat capacities γ=Cp/Cv • For an ideal gas internal energy change only depends on T so ΔU=nCvΔT no matter what the volume change is. • Example E l 19 19.6: 6 Find Fi d the th change h iin iinternal t l energy of a dorm room containing 2400 moles l off air i when h it iis cooled l d ffrom 23 23.9 90C tto 11.60C at a constant pressure of 1.00 atm. T t the Treat th air i as an ideal id l gas with ith γ=1.4. 14 Adiabatic Process for an ideal gas • Q=0 and ΔU=-W<0 • An adiabatic curve on PV diagram is always steeper than an isotherm. • Adiabatic process has to be fast for not letting heat exchange to happen. • If we use ideal g gas law to deduce any results the process has to be slow to allow equilibrium condition to b maintained. be i t i d • In reality it is hard to meet both of these conditions simultaneously So whatever simultaneously. we discuss here is an approximation. Adiabatic Process for an ideal gas • For an adiabatic process in an ideal gas: • TVγ-1=constant so T1V1γ-1= T2V2γ-1 • PVγ=constant so P1V1γ= P2V2γ • W=-ΔU=nCv (T1-T2) • Use PV=nRT PV nRT • W=Cv (P1V1-P2V2) /R (γ ) • W= ((P1V1-P2V2) /(γ-1) Summary Summary Summary Summary Example: 19.7 19 7 • The compression ratio of a diesel engine is 15 to 1 1. If the initial pressure is 1.01x105pa and the initial t temperature t is i 270C, C find fi d the final pressure and the temperature after compression. Air is a mixture of mostly diatomic oxygen and d nitrogen it th thatt is an ideal gas with γγ=1.40. ((T2=886K,, p2=44.8x105Pa=44 atm) Work done in an adiabatic process • In the previous example how much work is done by the gas do during the compression if the initial volume of the cylinder is 1.00 L=1.00x10-3m3? Assume that CV for air is 20.8 J/mol.K and γ=1.40