rppearso
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I have been working on a series of questions dealing with gas expansion and temperature change for my PE exam.
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The discussion revolves around gas expansion and temperature change, particularly in the context of preparing for the PE exam. Participants explore various equations and methodologies related to thermal expansion, Joule-Thomson expansion, and the application of equations of state.
Participants express various viewpoints and uncertainties regarding the methodologies for calculating temperature changes and the implications of using different equations of state. There is no consensus on the best approach or resolution to the issues raised.
Participants mention limitations in their understanding of certain concepts, such as the integrating factor in differential equations and the assumptions underlying their calculations. There are also references to specific resources, such as air tables and the chemical engineering PE exam book, which may not be universally familiar.
Individuals preparing for the PE exam, particularly those focused on thermodynamics, gas expansion, and related calculations, may find this discussion relevant.
rppearso said:I have been working on a series of questions dealing with gas expansion and temperature change for my PE exam.
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rppearso said:I am kinda working the thermal expansion of methanol in tandum with joule thompson expansion. I am studying for my PE right now (along with doing that thermal expansion of methanol at work) and I am having the same set of problems dealing with air, I attempted to use joule thompson to model rapid expansion of gas (the calcs under methanol expansion actually apply more to joule thompson rather than liquid expansion). If you view the work I did attached to thermal expansion of methanol (and I will also attach the mathcad and updated hand calcs) you will see that you get temperature trends opposite of what is expected and after going through the first law derivation and a bernoulli differential equation its pretty frustrating because it should be correct for the rapid expansion of a gas, I was doing this in order to develop an equation for T2 in terms of pressure change using a vander walls equation of state.
All that being said I need to progress with my PE study so I have just been using the air tables at the back of the PE book but I am not sure what Vr actually is. In an otto cycle in the constant volume expansion V is constant from D to A but Vr is not what exactly is Vr, we never used air tables in college and while I can crank out the PE problems using the methods in the book I would really like to know what it is I am doing.
This has been a very good site and I am glad I found it, it keeps me doing things that are useful and more away from political sites which just waste your time.
I have the updated joule thompson calcs worked out using the bernoulli differential equation (the roots of the methodology of solving first order non seperable differential equations will have to wait another day in a different section, but what is up with the integrating factor and why can you assume the constant of integration goes away, among other questions) and I will post them as soon as I can consolidate my work and scan everything in.
stewartcs said:Vr generally stands for Reduced Volume (i.e. The ratio of the specific volume of a substance to its critical volume). Not sure without seeing the book you are reading though.
CS