ThermodynamicsHard

Thermodynamic cycle (work and entropy)

n = 2 mol of an ideal gas at T₁ = 300 K perform a reversible cycle: isothermal compression from V₁ = 12 L to V₂ = 3 L, adiabatic expansion back to V₁, isochoric heating up to T₁. Find the work of the isotherm and the total entropy change over the cycle.
P V 1 2 3 T=cost Q=0
Given data
n = 2 molT₁ = 300 KV₁ = 12 L, V₂ = 3 LR = 8.314 J/mol·K
Review the theory: Termodinamica
Steps
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  1. In a reversible isothermal transformation the temperature is constant, so the work is the integral of p dV with p = nRT/V: L₁₂ = nRT₁·ln(V₂/V₁). Here it is a compression (V₂ < V₁), so the logarithm is negative: the work done by the gas is negative (the surroundings do work on the gas).
  2. Entropy is a state function: it depends only on the state of the system, not on the path. Over a cycle the system returns to its initial state, so its total entropy change is necessarily zero, whatever the individual transformations. What is ΔS over the cycle?
Full worked solution
  1. In a reversible isothermal transformation the temperature is constant, so the work is the integral of p dV with p = nRT/V: L₁₂ = nRT₁·ln(V₂/V₁). Here it is a compression (V₂ < V₁), so the logarithm is negative: the work done by the gas is negative (the surroundings do work on the gas).
    L12=nRT1ln⁡V2V1=2⋅8.314⋅300⋅ln⁡0.25L_{12} = nRT_1\ln\frac{V_2}{V_1} = 2\cdot8.314\cdot300\cdot\ln 0.25
    L12=4988⋅(−1.386)≈−6916 JL_{12} = 4988\cdot(-1.386) \approx \mathbf{-6916\,J} (compression → negative work).
  2. Entropy is a state function: it depends only on the state of the system, not on the path. Over a cycle the system returns to its initial state, so its total entropy change is necessarily zero, whatever the individual transformations. What is ΔS over the cycle?
    ΔScycle=0\Delta S_{cycle} = \mathbf{0}: entropy is a state function, so over a reversible cycle the total change is zero.
Result:L12≈−6.9L_{12} \approx -6.9 kJ, ΔScycle=0\Delta S_{cycle} = 0