For a one-component system open to particle exchange, Chapter 7's differential of the…

PHYSICS · Multi-part · Fermi University Physics · Thermal, Statistical & Complex Systems · Thermodynamic potentials and the formal structure of thermodynamics · Thermodynamic potentials and the formal structure of thermodynamics

Thermal Physics, Ch Chemical potential, open systems and chemical equilibrium

Problem

For a one-component system open to particle exchange, Chapter 7's differential of the Gibbs energy gains the chemical-potential term: dG=−S dT+V dp+μ dN\mathrm{d}G = -S\,\mathrm{d}T + V\,\mathrm{d}p + \mu\,\mathrm{d}N. Hydrogen may be treated as an ideal gas throughout. ((a)) By equating the mixed second derivatives of GG with respect to pp and NN, obtain a Maxwell relation between (∂μ/∂p)T,N(\partial\mu/\partial p)_{T,N} and a derivative of VV, and evaluate it for hydrogen at 350 K350\,\mathrm{K} and 2.00 bar=2.00×105 Pa2.00\,\mathrm{bar} = 2.00\times10^{5}\,\mathrm{Pa}. ((b)) Integrate that derivative at fixed temperature to find the change in μ\mu per molecule when the hydrogen is compressed from 2.00 bar2.00\,\mathrm{bar} to 5.00 bar5.00\,\mathrm{bar} at 350 K350\,\mathrm{K}. ((c)) Express the same change per mole, in J mol−1\mathrm{J\,mol^{-1}}. ((d)) 0.500 mol0.500\,\mathrm{mol} of that hydrogen at 350 K350\,\mathrm{K} and 5.00 bar5.00\,\mathrm{bar} is then mixed, at fixed temperature and pressure, with 0.500 mol0.500\,\mathrm{mol} of argon at the same temperature and pressure. Find the entropy of mixing.

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