U=Cv(dT) and Enthelphy=Cp(dt) for all processes in thermodynamics?

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SUMMARY

The discussion clarifies the relationships between internal energy (U), heat capacity at constant volume (Cv), enthalpy (H), and heat capacity at constant pressure (Cp) in thermodynamics. It establishes that for perfect gases, the equation dU=Cv(dT) holds true across all processes due to the zero value of the partial derivative of U with respect to volume at constant temperature. Additionally, it explains that dH=Cp(dT) applies in isobaric processes, reinforcing the concept that U and H are state functions dependent on two independent properties. The discussion emphasizes the importance of understanding these relationships for accurate thermodynamic calculations.

PREREQUISITES
  • Understanding of thermodynamic concepts such as internal energy and enthalpy.
  • Familiarity with heat capacities: Cv and Cp.
  • Knowledge of state functions in thermodynamics.
  • Basic calculus, specifically the chain rule for derivatives.
NEXT STEPS
  • Study the derivation of the first law of thermodynamics.
  • Learn about the implications of state functions in thermodynamic processes.
  • Explore the differences between Cv and Cp in various thermodynamic systems.
  • Investigate the applications of the ideal gas law in thermodynamic calculations.
USEFUL FOR

This discussion is beneficial for students and professionals in thermodynamics, including physicists, engineers, and anyone involved in energy systems analysis and optimization.

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Can someone explain why U=Cv(dT) and Enthalphy=Cp(dt) for all processes in thermodynamics?
 
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dQ=dU + dA => dU = dQ -dA , in isochoric processes dA = 0 so that dU=dQ(while V=const) =Cv*dT.
Enthalpy W is defined : W = U +PV => dW = dU +PdV +VdP = dU + dA + VdP = dQ + VdP, in isobaric processes dP=0 so dW=dQ (while P=const) =Cp*dT.
 
In thermodynamics you usually study systems with only one kind of work interation, so this means that two independent, intrinsic properties fix the state of the system. Since U and H are functions of state, that means a change in them can be expressed in terms of any two such variables. If we decide to determine U by temperature and volume, then the expression for an infintessimal change in U is, by the chain rule
dU=(\frac{\partial U} {\partial T})_VdT+(\frac{\partial U} {\partial V})_TdV
which, by definition of c_V is
dU=c_VdT+(\frac{\partial U} {\partial V})_TdV
So, dU is not always equal to c_VdT. However, for a perfect gas (\frac{\partial U} {\partial V})_T is always equal to zero, so that means that dU=c_Vdt for all processes involving perfect gases. That is probably what you meant. The dH equation is simmilar.

It seems strange at first that you would use the constant volume heat capacity for any process, including one at constant pressure. But this really isn't so strange. Fitrst of all, using c_P would make no sense to find \Delta U because this is defined as (\frac{\partial H} {\partial T})_P and notice that dU doesn't even appear there. Secondly, supposing the process is at constant pressure: U is a state function so we can imagine any path between the beginning and end points we want to compute \Delta U. Imagine the gas is first heated at constant volume. \Delta U for this process is clearly c_V\Delta T. Now let the gas expand at constant volume back to its original pressure. \Delta U for this process is (\frac{\partial U} {\partial V})_T \Delta V. But (\frac{\partial U} {\partial V})_T is zero for a perfect gas, so the total \Delta U is c_V \Delta T
 
wow! thanks! :)
 

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