Heat and the First Law of Thermodynamics
时间:2025-04-30
时间:2025-04-30
Ch.17 Heat and the First Law of Thermodynamics17.1 Heat as Energy Transfer 17.2 Internal Energy 17.3 Specific Heat 17.4 The First Law of Thermodynamics 17.5 Applying the First Law of Thermodynamics ; Calculating the Work 17.6 Molar Specific Heat for Gases, and the Equipartition of Energy 17.7 Adiabatic Expansion of a Gas The Absorption of Heat by Solids and Liquids 17.8* Heat Transfer; Conduction, Convection, Radiation
17.1 Heat as Energy TransferHeat is the energy that is transferred between one object and another object because of a temperature difference that exists between them.Heat Q , SI: J.
1cal 4.1860J1cal 3.969 10 3 Btu
Environment
“Calorie”
1Cal 1000cal 4186JHeat and work are not intrinsic properties of a system. They have meaning only as they describe the transfer of energy into or out of system.
17.2 Internal EnergyInternal Energy U of an Ideal GasThe total energy of a molecule For ideal gages EP 0 The total energy for N molecule
K EPU N NK1 3 2 K mv k T 2 2
For monatomic ideal gagesR k NAM tot N n N0 M mol
3 3 U N kT n R T 2 2
The internal energy U of an ideal gas is a function of the gas temperature only. U U ( T )
17.3 Specific Heat Heat CapacityQ C T C (T f Ti )dQ C dT
SI: J/K.
Specific HeatQ cm T cm(T f Ti )
dQ SI: J/kg.K. c m dTdQ Cm n dT SI: J/mol.K.
Molar Specific HeatQ nC m T nC m (T f Ti )
Molar Mass M = mNA , Avogadro’s Number NA=6.02 1023mol-1 Number of Moles n=Mtot/M
17.4 The First Law of Thermodynamics The quantity (Q – W) depends on the initial and final states (first law of thermodynamics ) U Q W
dU dQ dW (differential form of the first law ) The internal energy U of a system tends to increase if energy is added as heat Q and tends to decrease if energy is lost as work W done by the system.
Q W U U U 2 U1
the work done by a system W>0 the work done on a system W<0
17.5 Applying the First Law of Thermodynamics; Calculating the Work Work in a thermodynamic process with approximately thermal equilibrium(准静态)
dW F ds pAds pdVW dW Vf Vi
A: area of the surface
F
dV
ds F
pdV
p,V dV
p, V
Work on P-V Diagram
W dW The work done by a systemExpansion
Vf
Vi
pdV
The work done on a systemCompression
Vi
Vf
Vi
Vf
Work on P-V Diagram
dW dWigf icf
Wnet pdVL
Vi
Vf
Wighf Wicdf
Cyclical process
Work Done at Constant V and at Constant P The Constant-Volume Process (Isochoric Process)
V constant, WV 0
W
Vf
Vi
pdV
The Constant-Pressure Process (Isobaric Process) Isochoric
P constant, W p P ( V f Vi )
Isobaric
Work Done by an Ideal Gas at Constant TnRT T constant, p VWT Vf Vi
pdV
Vf
Vi
nRT dV V
Isothermpi
WT nRT
ln
Vf Vi
pf
(isothermal process)Pi WT nRT ln PfVi Vf
Example1(H.p.458) One mole of oxygen (ideal gas) expands at a constant temperature T of 310K from Vi = 12L to Vf = 19L. How much work is done by the gas during the expansion? Solution:
WT nRT ln
Vf Vi
19 1 8.31 310 ln 12 1180( J )
Adiabatic ProcessesQ=0
U W
A Graphical Summary of Four Gas Processes
Q1 Q2 Q3 Q4
T 200K ,Isobaric Isothermal
Isochoric
Adiabatic
Some Special Cases of the First Law of Thermodynamics
Q W UCyclical processes
U 0Qnet WnetFree expansions W=Q=0 U 0
Ti T f
Example 2(H.p.440) The figure here shows four paths on a p-V diagram along which a gas can be taken from state i to f. Rank the paths according to (a) the change U, (b) the work W done by the gas, and (c) the energy transferred as heat Q.Solution:
(a) All tie: U= Uf - U i (b) W
Vf
Vi
pdV
W 4> W 3 >W 2> W 1 (c) Q W U Q4> Q 3 >Q 2> Q 1ViVf
Example 3(H.p.442)
For one complete cycle as shown in the p-V diagram here, are (a) U for the gas and (b) the net transferred as heat Q positive, negative, or zero?.
Solution:
(a) Cyclical process : U= 0 (b)
Q W U U= 0
Q W 0
a state A to another state B and back again to A, via state C, as shown by path ABCA in the p-V diagram. (a) Complete the table. (b) Calculate the work done by the system for the complete cycle ABCA. Solution:
Example 4 (p.452-50) A thermodynamic system is taken from
Q W U(a)
U
W AB 0
0
W BC 0
WCA 0 ,
U CA 0
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