Ar (Gas) goes into spinner (Adiabatic Decompression): Power?

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Homework Help Overview

The discussion revolves around the adiabatic decompression of argon gas in a spinner system, where the gas is introduced at a specific mass flow rate, temperature, and pressure, and escapes at a lower pressure. Participants are tasked with determining the exit temperature, maximum power of the spinner, and hypothesizing the maximum efficiency of the system.

Discussion Character

  • Exploratory, Conceptual clarification, Problem interpretation, Assumption checking

Approaches and Questions Raised

  • Participants discuss the calculations for the exit temperature and question the validity of their methods, particularly regarding the treatment of the system as closed versus open. There are attempts to derive relationships between temperature and pressure for adiabatic processes, and some participants express confusion over the definitions and equations involved.

Discussion Status

Some participants have successfully calculated the exit temperature but express uncertainty about their approach and the assumptions made. There is ongoing exploration of the equations needed to find the maximum power and efficiency, with references to the first law of thermodynamics and the need for a better understanding of open system dynamics. Multiple interpretations of the problem setup are being considered.

Contextual Notes

Participants note discrepancies in the density of the gas and the significance of using appropriate thermodynamic equations. There is a mention of potential confusion regarding the relationship between internal energy and work, as well as the need for foundational knowledge in thermodynamics to address the problem effectively.

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Homework Statement



Argo, in its gas form, is insterted into a spinner, with a rhythm of 80.0 kg/min = 1.33 kg/s, temperature 800 C (= 1073.15 K), and pressure 1.50 MPa. It's decompressed adiabatically, and "escapes" the spinner with pressure 300 kPa.

a) Temperature when it "escapes" ?
b) Maximum Power of the spinner?
c) Hypothesize that the spinner works as a machine that completes a "closedcircle" when a gas is inserted. What's the maximum efficiency of this machine?

Homework Equations



p = m/V
PVγ = constant
TVγ-1 = constant
PV = nRT
ec = 1 - Tc/Th

γ = 1.67 (from the book)
p = 1784 kg/m3

The Attempt at a Solution



a) That one I've solved:

>Gas is inserted with a rhythm of 1.33 kg/s. So, mi = 1.33 kg.

>p = m/V = 1784 kg/m3

>Therefore, Vi = 7.45 * 10-4 m3

>PiViγ = PfVfγ <=> ... <=> Vf = 1.95 * 10-3 m3

>TiViγ-1 = TfVfγ-1 <=> ... <=> Tf = 563 K

The book's answer is 564 K, but to it flactuates between using Tk = Tc + 273.15 and Tk = Tc + 273,and it plays fast and loose with the Significant Digits. Not to mention that with Tf = 564 K, (c)'sresultis still not in line with the book's.

b) That's where I'm stuck. I know that Power is given through P = W/Δt, but I've got no clue one how to find the Work. I figured I'd do this:

W = ∫ViVfPdV, with P = PiViγ/Vγ, but I got a wholly different result.

c) The machine will have a maximum efficiency if it works like a Carnotone, so:

ec = 1 - Tc/Th = 1 - 563 K/1073.15 K = 0.475 = 47.5 %

Any help is appreciated!
 
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Darthkostis said:

Homework Statement



Argo, in its gas form, is insterted into a spinner, with a rhythm of 80.0 kg/min = 1.33 kg/s, temperature 800 C (= 1073.15 K), and pressure 1.50 MPa. It's decompressed adiabatically, and "escapes" the spinner with pressure 300 kPa.

a) Temperature when it "escapes" ?
b) Maximum Power of the spinner?
c) Hypothesize that the spinner works as a machine that completes a "closedcircle" when a gas is inserted. What's the maximum efficiency of this machine?

Homework Equations



p = m/V
PVγ = constant
TVγ-1 = constant
PV = nRT
ec = 1 - Tc/Th

γ = 1.67 (from the book)
p = 1784 kg/m3

The Attempt at a Solution



a) That one I've solved:

>Gas is inserted with a rhythm of 1.33 kg/s. So, mi = 1.33 kg.

>p = m/V = 1784 kg/m3

>Therefore, Vi = 7.45 * 10-4 m3

>PiViγ = PfVfγ <=> ... <=> Vf = 1.95 * 10-3 m3

>TiViγ-1 = TfVfγ-1 <=> ... <=> Tf = 563 K

The book's answer is 564 K, but to it flactuates between using Tk = Tc + 273.15 and Tk = Tc + 273,and it plays fast and loose with the Significant Digits. Not to mention that with Tf = 564 K, (c)'sresultis still not in line with the book's.
Even though you got the correct answer for the exit temperature (563 K), this was not analyzed correctly. You can't just take the mass flow rate in a continuous flow turbine and treat the turbine as a closed system containing the amount of mass that flows through in one second. And the density of the gas is, of course, not 1784 kg/m^3; this is nearly twice the density of liquid water. The equation you should have used was $$\frac{T_f}{T_i}=\left(\frac{P_f}{P_i}\right)^{\frac{\gamma-1}{\gamma}}\tag{1}$$This can be derived from a combination of the ideal gas law with the equation $$P_fV_f^{\gamma}=P_iV_i^{\gamma}$$See if you can derive Eqn. 1.
b) That's where I'm stuck. I know that Power is given through P = W/Δt, but I've got no clue one how to find the Work. I figured I'd do this:

W = ∫ViVfPdV, with P = PiViγ/Vγ, but I got a wholly different result.
To get the power delivered by the turbine (rate of doing shaft work) in this continuous flow process (operating at steady state), you need to use the open system (control volume) version of the first law of thermodynamics. Are you familiar with this equation?
 
Chestermiller said:
Even though you got the correct answer for the exit temperature (563 K), this was not analyzed correctly.

Darn it.

Chestermiller said:
You can't just take the mass flow rate in a continuous flow turbine and treat the turbine as a closed system containing the amount of mass that flows through in one second.

Yeah, it seemed weird to me as well, but I got the right result, so I figured I had to be doing something right. Generally I just thought "hey, as soon as I open the turbine this mass enters" and treated that as "the initial mass". Pretty faulty logic though, yeah.

Chestermiller said:
And the density of the gas is, of course, not 1784 kg/m^3; this is nearly twice the density of liquid water.

I looked it up on Wikipedia, but I messed up on the conversion part. Yeah, you're right.

Chestermiller said:
The equation you should have used was $$\frac{T_f}{T_i}=\left(\frac{P_f}{P_i}\right)^{\frac{\gamma-1}{\gamma}}\tag{1}$$This can be derived from a combination of the ideal gas law with the equation $$P_fV_f^{\gamma}=P_iV_i^{\gamma}$$See if you can derive Eqn. 1.

I tried, and I didn't make it, but I foundthe proof at Wikipedia, here: https://en.wikipedia.org/wiki/Adiabatic_process
I don't get this part though: ΔU = aRnT2 - aRnT1 = aRnΔT. What is the "a"? Why does he use internal energy? My book doesn't mention anything about that (the whole thermodynamics section deals with ΔE & W). Are Q & ΔU connected in some way? I get the rest of the thought process.

Chestermiller said:
To get the power delivered by the turbine (rate of doing shaft work) in this continuous flow process (operating at steady state), you need to use the open system (control volume) version of the first law of thermodynamics. Are you familiar with this equation?

No, not really. I searched around a bit, but I didn't find anything that I recognized.
 
Darthkostis said:
I tried, and I didn't make it, but I foundthe proof at Wikipedia, here: https://en.wikipedia.org/wiki/Adiabatic_process
I don't get this part though: ΔU = aRnT2 - aRnT1 = aRnΔT. What is the "a"? Why does he use internal energy? My book doesn't mention anything about that (the whole thermodynamics section deals with ΔE & W). Are Q & ΔU connected in some way? I get the rest of the thought process.
I don't want to go off in a tangent on the derivation of the thermodynamics relationships for adiabatic reversible expansion of an ideal gas in a closed system. I want to keep the focus on the open system problem at hand. If you have questions about the derivation in Wikipedia, please start a new thread under General Physics.

For the relationship I was referring to in my previous post starting with $$P_fV_f^{\gamma}=P_iV_i^{\gamma}$$
we have (using the ideal gas law) $$P_f\left(\frac{RT_f}{P_f}\right)^{\gamma}=P_i\left(\frac{RT_i}{P_i}\right)^{\gamma}$$
Simplifying this leads to $$P_f^{(1-\gamma)}T_f^\gamma=P_i^{(1-\gamma)}T_i^\gamma$$
This leads to $$\frac{T_f}{T_i}=\left(\frac{P_f}{P_i}\right)^{\frac{\gamma-1}{\gamma}}$$

No, not really. I searched around a bit, but I didn't find anything that I recognized.
This problem should never have been assigned to you if you have not yet learned about the open system version of the first law of thermodynamics. You really need it to solve this problem. And Physics Forums is not an appropriate location for the derivation; it is presented in virtually every elementary thermodynamics book. For good references, see Fundamentals of Engineering Thermodynamics by Moran et al and Introduction to Chemical Engineering Thermodynamics by Smith and Van Ness.
 
Chestermiller said:
I don't want to go off in a tangent on the derivation of the thermodynamics relationships for adiabatic reversible expansion of an ideal gas in a closed system. I want to keep the focus on the open system problem at hand. If you have questions about the derivation in Wikipedia, please start a new thread under General Physics.

For the relationship I was referring to in my previous post starting with $$P_fV_f^{\gamma}=P_iV_i^{\gamma}$$
we have (using the ideal gas law) $$P_f\left(\frac{RT_f}{P_f}\right)^{\gamma}=P_i\left(\frac{RT_i}{P_i}\right)^{\gamma}$$
Simplifying this leads to $$P_f^{(1-\gamma)}T_f^\gamma=P_i^{(1-\gamma)}T_i^\gamma$$
This leads to $$\frac{T_f}{T_i}=\left(\frac{P_f}{P_i}\right)^{\frac{\gamma-1}{\gamma}}$$

Oh yeah, that makes sense. I just figured that since my book used integrations to prove TVγ-1 = constant, I figured I'd need to do the same here.
Chestermiller said:
This problem should never have been assigned to you if you have not yet learned about the open system version of the first law of thermodynamics. You really need it to solve this problem. And Physics Forums is not an appropriate location for the derivation; it is presented in virtually every elementary thermodynamics book. For good references, see Fundamentals of Engineering Thermodynamics by Moran et al and Introduction to Chemical Engineering Thermodynamics by Smith and Van Ness.

Yeah, I searched again, but I really don't know it, and it's not in my book. Thanks for the sources though, I'll try and find them sometime.

Anyway, thanks for all the help!
 

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