Reversible, Isothermal Compression from P1 to P2. How much heat?

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SUMMARY

This discussion focuses on calculating the heat transfer during a reversible, isothermal compression process from pressure P1 to P2. The solution utilizes Maxwell's relations and the differential forms of thermodynamic potentials, specifically emphasizing the relationship between entropy (S), temperature (T), and pressure (P). The key equation derived is dQ = -T(dV/dT)P dP, leading to the integral Q = T ∫ dQ between P1 and P2. The discussion highlights the importance of understanding state functions in thermodynamics.

PREREQUISITES
  • Understanding of Maxwell's relations in thermodynamics
  • Familiarity with thermodynamic potentials: Internal Energy, Enthalpy, Gibbs Free Energy, Helmholtz Free Energy
  • Knowledge of partial derivatives and their application in thermodynamic equations
  • Concept of isothermal processes and their implications in heat transfer
NEXT STEPS
  • Study the derivation and application of Maxwell's relations in thermodynamics
  • Explore the implications of isothermal processes in real-world applications
  • Learn about the differential forms of thermodynamic potentials in detail
  • Investigate the role of state functions in thermodynamic calculations
USEFUL FOR

This discussion is beneficial for students and professionals in thermodynamics, particularly those studying heat transfer, reversible processes, and the application of Maxwell's relations in engineering and physical sciences.

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Homework Statement



Compress a body reversibly and isothermally from P1 to P2. How much heat goes in or out?

Homework Equations



Maxwells four relations, differential forms of the four thermodynamic potentials (Central, Enthalpy, Gibbs, Helmholtz)

The Attempt at a Solution



My problem is that I've been told that the way this is done is saying that S=S(T,P) therefore dS=(dS/dT)P dT + (dS/dP)T dP Isothermal hence dS= second term and using the fourth maxwell relation you can rewrite it as:

dS = - (dV/dT)P dP and since it is reversible we have dQ=TdS so dQ = -T(dV/dT)P dP [The derivatives inside the brackets are partial derivatives]

Integrating gives: Q = T ∫ dQ between P1 and P2.

The first part of this solution seems fishy where we say that S=S(T,P) I understand that this is still a function of state, however when deriving the Maxwell relations we used either the central equation and the other differential forms of the thermodynamic potentials to give us an idea of what something was a function of e.g. U=U(S,V) since dU=TdS-PdV
 
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