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How to better understand thermodynamics? With statistical mechanics? |
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| Jun14-07, 07:06 PM | #1 |
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How to better understand thermodynamics? With statistical mechanics?
Does anyone understand thermodynamics? There are so many terms that I feel that I am doing the maths but not really understanding the physics.
Is it better to do stuff from a stat physics way (which makes more sense) and derive the thermodynamic relations from there? |
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| Jun15-07, 08:12 AM | #2 |
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I was a bit stunned as I was reviewing my notes from a 3 week break. I then reviwed 1st year thermodynamics material and the stuff came back to me a bit and now I am back into it again. So there is physical understanding after all.
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| Jun15-07, 08:24 AM | #3 |
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Yes - people, particularly physicists and many engineers, understand thermodynamics. It does help to have a firm grounding in basic physics, particular an understanding of energy/work and momentum, and force.
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| Jun15-07, 07:39 PM | #4 |
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How to better understand thermodynamics? With statistical mechanics?
It seems that the concept of potential energy doesn't arise in thermodynamics because of the huge number of atoms in the system. Or is it because thermodynamics deals with equilibrium situations and so no foce is acted on the system (i.e. forces all cancel).
Or is it because the system is not usually conserved as the 1nd law suggests that total energy of the system can change. So keeping a potential energy in the system would be meaningless. It is only meaningful to account for the kinetic energy of molecules which comes into full fruition when relating it to the temperture in the system. |
| Jun15-07, 07:47 PM | #5 |
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| Jun15-07, 08:17 PM | #6 |
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Oh, dear. Please open your thermo book and reread it cover to cover.
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| Jun15-07, 08:34 PM | #7 |
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what about studying thermodynamics from a chemistry perspective?
that might help you get a more conceptual understanding. |
| Jun15-07, 09:28 PM | #8 |
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Mentor
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If you mean potential energy in terms of a compressed gas, it's the same. You convert it to kinetic energy (minus the ever-present entropy), but the total stays the same. |
| Jun15-07, 11:20 PM | #9 |
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| Jun15-07, 11:32 PM | #10 |
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The 1st law is an extension of the isolated system and considering a system inside a larger system, i.e. bath or universe. Hence the system as oppossed to the bath is not isolated. That is much more realistic wouldn't you say? If the system dosen't interact with the surrounding than the 1st law is reduced to the isolated system's case of total energy = constant. In fact it makes a lot of sense because suppose we had an oscillating spring in an air filled room. If we let it oscillate by starting its position from a non equilibrium position, it will eventually slow down because it is doing work on the air molecules hence losing total energy. It is directly losing kinetic energy thereby not springing to as far a distance as before hence decreasing its potential energy as well and the cycle spirals until no energy is left. |
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