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

In summary, the two equations for thermodynamics are U=Cv(dT) and Enthalphy=Cp(dt). In isochoric processes, dA=0 so dU=dQ(while V=const). In isobaric processes, dP=0 so dW=dQ. 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.
  • #1
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Can someone explain why U=Cv(dT) and Enthalphy=Cp(dt) for all processes in thermodynamics?
 
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  • #2
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.
 
  • #3
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
[tex]dU=(\frac{\partial U} {\partial T})_VdT+(\frac{\partial U} {\partial V})_TdV[/tex]
which, by definition of [itex]c_V[/itex] is
[tex]dU=c_VdT+(\frac{\partial U} {\partial V})_TdV[/tex]
So, dU is not always equal to [itex]c_VdT[/itex]. However, for a perfect gas [tex](\frac{\partial U} {\partial V})_T[/tex] is always equal to zero, so that means that [itex]dU=c_Vdt[/itex] 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 [itex]c_P[/itex] would make no sense to find [itex]\Delta U[/itex] because this is defined as [itex](\frac{\partial H} {\partial T})_P[/itex] 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 [itex]\Delta U[/itex]. Imagine the gas is first heated at constant volume. [itex]\Delta U[/itex] for this process is clearly [itex]c_V\Delta T[/itex]. Now let the gas expand at constant volume back to its original pressure. [itex]\Delta U[/itex] for this process is [itex](\frac{\partial U} {\partial V})_T \Delta V[/itex]. But [itex](\frac{\partial U} {\partial V})_T[/itex] is zero for a perfect gas, so the total [itex]\Delta U[/itex] is [itex] c_V \Delta T[/itex]
 
  • #4
wow! thanks! :)
 

1. What is the meaning of the equation U=Cv(dT) in thermodynamics?

The equation U=Cv(dT) represents the internal energy of a system, where U is the internal energy, Cv is the heat capacity at constant volume, and dT is the change in temperature. This equation is used to calculate the change in internal energy of a system during a process where the volume remains constant.

2. How is the equation Enthalpy=Cp(dt) used in thermodynamics?

The equation Enthalpy=Cp(dt) represents the change in enthalpy of a system, where Enthalpy is the total heat content of the system, Cp is the heat capacity at constant pressure, and dt is the change in temperature. This equation is used to calculate the change in enthalpy of a system during a process where the pressure remains constant.

3. What is the significance of the heat capacity in these equations?

The heat capacity, represented by Cv and Cp in the equations, is a measure of the amount of heat required to raise the temperature of a substance by a certain amount. It is an important factor in thermodynamics as it helps determine the amount of energy needed for a system to undergo a temperature change.

4. Can these equations be applied to all processes in thermodynamics?

Yes, these equations can be applied to all processes in thermodynamics as long as the conditions of the process are constant. U=Cv(dT) is applicable for processes where the volume remains constant, while Enthalpy=Cp(dt) is applicable for processes where the pressure remains constant.

5. How are these equations derived and what are their limitations?

These equations are derived from the first law of thermodynamics, which states that the change in internal energy of a system is equal to the heat added to the system minus the work done by the system. Their limitations include assuming ideal conditions and constant properties, and they may not accurately predict the behavior of real-world systems.

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