- #1
S. Moger
- 53
- 2
I am preparing for a re-exam, this is a problem from the exam I took, but I can't see what I did wrong and why.
Case: A turbine that is producing work dW is powered by compressed air (treated as a diatomic ideal gas).
Known quantities:
[itex]P_0, P_f, T_0[/itex]
Wanted quantity:
[itex]dW[/itex] per mole air.
It is also known that the process is adiabatic, so [itex]dQ = 0[/itex], and that the flow is stationary.
By the first law of thermodynamics, and the adiabatic property:
[itex]\Delta U = dQ + dW = dW[/itex].
The energy content of a diatomic ideal gas is given by:
[itex]U = \frac{f}{2} nRT[/itex], where f = 5 (the amount of quadratic degrees of freedom)
Thus, ΔU should equal the change in energy content of the air before and after the turbine:
[itex]\Delta U = U_0 - U_f =\frac{f}{2} nR (T_0 - T_f) = dW [/itex].
To compute the unknown [itex]T_f[/itex] we again use the fact that the process is adiabatic, so the following should hold
[itex]P_0^{-\frac{2}{f+2}} T_0 = P_f^{-\frac{2}{f+2}} T_f \iff T_f = T_0 (\frac{P_f}{P_0})^{\frac{2}{f+2}}[/itex].
Inserting this result into the prior equation gives
[itex]\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW[/itex] per mole (with n=1).
_________________________________
However, the solution sheet states that the term f/2=5/2 should be 7/2 (rest unchanged). I can't see why. They use a different technique as well, which I don't understand.
The correct solution:
Stationary flow implies that [itex] H_0 = W + H_f[/itex] by the first law of thermodynamics. The enthalpy [itex]H=C_P T[/itex]. So, [itex]W=C_P (T_0 - T_f)[/itex]. Furthermore,
[itex]T_f = T_0 (\frac{P_f}{P_0})^{1-1/\gamma}[/itex] and
[itex]C_P = 7/2 nR[/itex] by the properties of diatomic ideal gases.
Finally,
[itex]W/n = \frac{7}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{1-1/\gamma})[/itex]
_________________________________
which is not what I get:
[itex]\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW[/itex] per mole (with n=1).
Gamma is defined as (f+2)/f. Also observe that their notation is W instead of dW ( which here is not meant to be read as a change in work, but a quantity of work ).
Homework Statement
Case: A turbine that is producing work dW is powered by compressed air (treated as a diatomic ideal gas).
Known quantities:
[itex]P_0, P_f, T_0[/itex]
Wanted quantity:
[itex]dW[/itex] per mole air.
It is also known that the process is adiabatic, so [itex]dQ = 0[/itex], and that the flow is stationary.
Homework Equations
The Attempt at a Solution
By the first law of thermodynamics, and the adiabatic property:
[itex]\Delta U = dQ + dW = dW[/itex].
The energy content of a diatomic ideal gas is given by:
[itex]U = \frac{f}{2} nRT[/itex], where f = 5 (the amount of quadratic degrees of freedom)
Thus, ΔU should equal the change in energy content of the air before and after the turbine:
[itex]\Delta U = U_0 - U_f =\frac{f}{2} nR (T_0 - T_f) = dW [/itex].
To compute the unknown [itex]T_f[/itex] we again use the fact that the process is adiabatic, so the following should hold
[itex]P_0^{-\frac{2}{f+2}} T_0 = P_f^{-\frac{2}{f+2}} T_f \iff T_f = T_0 (\frac{P_f}{P_0})^{\frac{2}{f+2}}[/itex].
Inserting this result into the prior equation gives
[itex]\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW[/itex] per mole (with n=1).
_________________________________
However, the solution sheet states that the term f/2=5/2 should be 7/2 (rest unchanged). I can't see why. They use a different technique as well, which I don't understand.
The correct solution:
Stationary flow implies that [itex] H_0 = W + H_f[/itex] by the first law of thermodynamics. The enthalpy [itex]H=C_P T[/itex]. So, [itex]W=C_P (T_0 - T_f)[/itex]. Furthermore,
[itex]T_f = T_0 (\frac{P_f}{P_0})^{1-1/\gamma}[/itex] and
[itex]C_P = 7/2 nR[/itex] by the properties of diatomic ideal gases.
Finally,
[itex]W/n = \frac{7}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{1-1/\gamma})[/itex]
_________________________________
which is not what I get:
[itex]\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW[/itex] per mole (with n=1).
Gamma is defined as (f+2)/f. Also observe that their notation is W instead of dW ( which here is not meant to be read as a change in work, but a quantity of work ).
Last edited: