Turn P^a V^b = Constant into a Heat Capacity
A polytropic process follows P V^x = constant. Isobaric, isochoric, isothermal and adiabatic processes are all special cases, and for any x the molar heat capacity, the work done and the way temperature changes follow from one formula.
Polytropic Processes is the central idea in this question pattern. Identify the condition in the stem before applying the method below.
Molar heat capacity in a polytropic process
It reduces correctly in the special cases: x = 0 (isobaric) gives Cv + R = Cp, x = γ (adiabatic) gives zero, x = 1 (isothermal) gives infinity, and very large x (isochoric) gives Cv. For one mole of a monatomic gas with PV⁵ = constant, C = 3R/2 + R/(1 - 5) = 3R/2 - R/4 = 5R/4.
Which way does the temperature go?
If x is less than 1, temperature rises as the gas expands, so internal energy rises with it; if x is greater than 1, the temperature falls on expansion.
Work in a polytropic or power-law process
The same trick (replace the power of V by RT/P or RT/a) converts any power-law work into a function of the temperature change.
Heat capacity from the heat-to-work ratio
If a diatomic gas does work Q/4 when heat Q is supplied, then ΔU = Q - Q/4 = 3Q/4 and the heat capacity is C = Q/(n ΔT) = (4/3) Cv = (4/3)(5R/2) = 10R/3. Always find ΔU from the first law, relate it to n Cv ΔT, and then divide the supplied heat by n ΔT.
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- ✓For P V^x = constant: C = Cv + R/(1 - x); x = 0, 1, γ and infinity give Cp, infinity, 0 and Cv
- ✓Rewrite P^a V^b = constant as P V^(b/a) = constant to find x
- ✓T is proportional to V^(1 - x); for x < 1 expansion raises temperature and internal energy
- ✓For P proportional to V², W = R(T2 - T1)/3 for one mole
- ✓With a given heat-to-work ratio, get ΔU from the first law and then C = Q/(n ΔT)
Do not read the exponent on P as the polytropic index. In P²V = constant the index of V is 1/2 only after you take the square root of the whole relation; applying C = Cv + R/(1 - x) with x = 2 or x = 1 gives a wrong heat capacity.
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