How to better understand thermodynamics? With statistical mechanics?

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Discussion Overview

The discussion revolves around understanding thermodynamics, particularly in relation to statistical mechanics. Participants explore various perspectives on how to grasp the concepts of thermodynamics, including the role of potential energy, the first law of thermodynamics, and the relationship between microscopic and macroscopic descriptions of systems.

Discussion Character

  • Exploratory
  • Debate/contested
  • Technical explanation

Main Points Raised

  • Some participants express difficulty in understanding thermodynamics despite being able to perform calculations, suggesting a need for a deeper conceptual grasp.
  • One participant proposes that studying thermodynamics from a statistical physics perspective might provide clearer insights into thermodynamic relations.
  • Another participant reflects on their own experience, noting that reviewing earlier material helped them regain physical understanding of the concepts.
  • There is a discussion about the relevance of potential energy in thermodynamics, with some arguing that it is not significant due to the large number of atoms involved and the focus on equilibrium states.
  • Some participants challenge the interpretation of the first law of thermodynamics, particularly regarding the conservation of energy in isolated versus non-isolated systems.
  • One participant emphasizes that while the total energy of an isolated system must be conserved, the energy of a system can change when considering heat and work interactions with a larger system.
  • There is a debate about the implications of large numbers of atoms on the treatment of energy, with some suggesting that individual trajectories become less relevant in large systems.

Areas of Agreement / Disagreement

Participants do not reach consensus on several points, particularly regarding the interpretation of the first law of thermodynamics and the role of potential energy in thermodynamic systems. Multiple competing views remain on these topics.

Contextual Notes

Some participants express uncertainty about the definitions and implications of potential energy in thermodynamics, as well as the conditions under which the first law applies. There are also references to the complexities introduced by considering systems that interact with their surroundings.

pivoxa15
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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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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.
 
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.
 
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.
 
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pivoxa15 said:
as the 1nd law suggests that total energy of the system can change.
Huh? That's not the 1st law that I remember.
 
Oh, dear. Please open your thermo book and reread it cover to cover.
 
what about studying thermodynamics from a chemistry perspective?

that might help you get a more conceptual understanding.
 
pivoxa15 said:
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).
I'm not sure what the number of atoms has to do with anything, but if you mean gravitational potential energy, it can come into play but doesn't often because you don't generally have large changes in elevation with basic thermodynamic cycles.
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.
Huh? Total energy of an isolated system must be conserved. That's what the first law says. If you drop a rock off a cliff, you convert potential energy to kinetic, during the fall, the total energy never changes.

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.
 
cesiumfrog said:
Huh? That's not the 1st law that I remember.

Change in U=Q-W. So yes, the total energy of the system can change according to how much heat and work that has occurred in the larger system (the system is a subset of the larger system). However the total energy in the larger system (i.e universe) is usually constant.
 
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russ_watters said:
I'm not sure what the number of atoms has to do with anything,

The book suggested that when the number of atoms is large, the individual trajectories of atoms are discarded. Normally in smaller system accounting for a countable number of particles with forces, it is convenient to use kinetic and potential energy if the system is isolated.
russ_watters said:
Huh? Total energy of an isolated system must be conserved. That's what the first law says. If you drop a rock off a cliff, you convert potential energy to kinetic, during the fall, the total energy never changes.
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 doesn't interact with the surrounding than the 1st law is reduced to the isolated system's case of total energy = constant.
russ_watters said:
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.

So this would be the case of a gas trapped inside a cyclinder without any outside contact. However W can be nonzero as the gas expands and contracts but is 0 if the system is inside a vacuum. Q=0 always in this case.

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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