Thermal Physics Flashcards

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1
Q

Thermal expansion coefficient

A

B = 1/V*dV/dT = d(lnV)/dT

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2
Q

Fourier’s heat conduction law

A

Rate of heat flow = q(dot) = -kA*dt/dx

k is thermal conductivity.

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3
Q

Virial Equations of State

A

PV = nRT(1+B/(V/n) + C/(V/n)^2)

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4
Q

Approximation of e^-x for small x

A

e^-x = 1-x for small x

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5
Q

Van der Waals equation

A

P=nRT/(V-nb)-a(n/v)^2

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6
Q

Equipartition theorem

A

At temperature T, the average energy of any quadratic degree of freedom is kT/2.

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7
Q

Total thermal energy

A

U = NfkT/2

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8
Q

First law

A

deltaU = q+w

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9
Q

Adiabatic process

A

No heat transfer between system and surroundings. q=0.

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10
Q

Isothermal

A

deltaU = 0

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11
Q

Max work

A

Available when change takes place reversibly

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12
Q

Isothermal + reversible

A

deltaU = 0, q = -w = nRT*ln(Vf/Vi)

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13
Q

heat capacities

A

c(v) = q(v)/deltaT = deltaU/deltaT, c(p)=q(p)/deltaT

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14
Q

Work in terms of heat capacity

A

w=nc(v)deltaT
work + means work done on the gas, compression, T of gas increases
work - means work done by the gas, expansion, T of gas decreases

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15
Q

Latent Heat

A

q = mL

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16
Q

Enthalpy

A

H = U+PV

17
Q

Virial Theorem

A

In any system where particles are held together by mutual gravitational attraction: U(potential) = -2U(kinetic)

18
Q

Adiabatic expansion/compression of ideal gas

A
PV^gamma = constant
gamma = (f+2)/f = c(p)/c(v)
c(p) = c(v)+R
19
Q

Mechanical equilibrium

A

Net force = 0

20
Q

Temperature

A

A measure of how easily the multiplicity of the system changes with energy

21
Q

Stirling’s approximation

A

ln(N!) = NlnN - N

22
Q

Approximation of ln(1+x) for small x

A

ln(1+x) = x for small x

23
Q

Second law

A

Any large system in equilibrium will be found in the macrostate with greatest entropy

24
Q

Boltzmann’s equation

A

S = kln(multiplicity) in J/K

25
Q

Spontaneous

A

deltaS > 0

26
Q

High temp, large N, entropy estimate

A

S = Nk(ln(q/N)+1)

27
Q

In Einstein solid or ideal gas, entropy estimate

A

S = Nk

28
Q

Sackur-Tetrode equation

A

S = Nk(ln(V/N((4pimU)/(3Nh^2))^(3/2))+5/2)

29
Q

Entropy of mixing

A
deltaS(A) = N(A)kln(((V(A)+V(B))/V(A))
deltaS(B) = N(B)kln(((V(A)+V(B))/V(B))
deltaS(mix) = deltaS(A)+deltaS(B) = 2Nkln2
30
Q

Isentropic

A
deltaS = 0
Isentropic = adiabatic + mechanically reversible
31
Q

Thermodynamic identity

A

dU = TdS-PdV+(mu)dN

32
Q

Thermal interaction

A

1/T = PartialS/PartialU at constant V,N

33
Q

Mechanical interaction

A

P/T = PartialS/PartialV at constant U,N

34
Q

Diffusive interaction

A

(mu)/T = - PartialS/PartialN at constant U,V

35
Q

Third law

A

Systems cannot absorb energy at T=0. Systems cannot exceed their temperature at maximum entropy. Occurs in systems with finite numbers of energy levels, or a maximum energy U.

36
Q

Curie’s Law

A
M = (mu)(N(up)-N(down)) 
M = N(mu)tanh((mu*B)/kT)
M = -U/B
tanh(x) = (e^x-e^(-x))/(e^x+e^(-x))
37
Q

Change in entropy of surroundings

A
deltaS(surroundings) = -q/T(surroundings)
q = U/hfN ? hf is energy difference between ground and excited state