S. Moger
- 52
- 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:
P_0, P_f, T_0
Wanted quantity:
dW per mole air.
It is also known that the process is adiabatic, so dQ = 0, and that the flow is stationary.
By the first law of thermodynamics, and the adiabatic property:
\Delta U = dQ + dW = dW.
The energy content of a diatomic ideal gas is given by:
U = \frac{f}{2} nRT, 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:
\Delta U = U_0 - U_f =\frac{f}{2} nR (T_0 - T_f) = dW.
To compute the unknown T_f we again use the fact that the process is adiabatic, so the following should hold
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}}.
Inserting this result into the prior equation gives
\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW per mole (with n=1).
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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 H_0 = W + H_f by the first law of thermodynamics. The enthalpy H=C_P T. So, W=C_P (T_0 - T_f). Furthermore,
T_f = T_0 (\frac{P_f}{P_0})^{1-1/\gamma} and
C_P = 7/2 nR by the properties of diatomic ideal gases.
Finally,
W/n = \frac{7}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{1-1/\gamma})
_________________________________
which is not what I get:
\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW 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:
P_0, P_f, T_0
Wanted quantity:
dW per mole air.
It is also known that the process is adiabatic, so dQ = 0, and that the flow is stationary.
Homework Equations
The Attempt at a Solution
By the first law of thermodynamics, and the adiabatic property:
\Delta U = dQ + dW = dW.
The energy content of a diatomic ideal gas is given by:
U = \frac{f}{2} nRT, 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:
\Delta U = U_0 - U_f =\frac{f}{2} nR (T_0 - T_f) = dW.
To compute the unknown T_f we again use the fact that the process is adiabatic, so the following should hold
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}}.
Inserting this result into the prior equation gives
\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW 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 H_0 = W + H_f by the first law of thermodynamics. The enthalpy H=C_P T. So, W=C_P (T_0 - T_f). Furthermore,
T_f = T_0 (\frac{P_f}{P_0})^{1-1/\gamma} and
C_P = 7/2 nR by the properties of diatomic ideal gases.
Finally,
W/n = \frac{7}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{1-1/\gamma})
_________________________________
which is not what I get:
\Delta U = \frac{f}{2} R T_0 ( 1 - (\frac{P_f}{P_0})^{\frac{2}{f+2}}) = dW 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 ).
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