Conflicting definition of degree of freedom in Kinetic Theory of Gases

In summary, the excerpt from the textbook is formatted inaccurately and can be misleading to students. I recommend using another book to learn about statistical physics.
  • #1
vcsharp2003
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Is degree of freedom just an independent term/variable/coordinate or the number of independent terms/variables/coordinates?
I am seeing conflicting definitions of degree of freedom in my textbook. If I look at the definition given as per screenshot below then it is the number of independent terms/variables/coordinates used to define the energy of a molecule. But, if I look at the statement of Equipartition of energy that is given below the definition, then it seems that degree of freedom is any one of independent terms/variables/coordinates used to get energy of a molecule.

I think degree of freedom should just be the independent term/variable/coordinate.

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  • #2
Why do you think the two paragraphs conflict?
 
  • #3
Doc Al said:
Why do you think the two paragraphs conflict?
The first paragraph says that degree of freedom is the number of independent variables.

The second paragraph is is meaning degree of freedom to be the independent variable.
 
  • #4
Ah, I think I see what you're saying. I can appreciate the confusion.

I would have said something like: A monatomic gas molecule has three degrees of freedom, a diatomic molecule has five, etc. And the equipartition of energy gives the average energy associated with each degree of freedom.
 
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  • #5
For me the excerpt from the book is formulated so inaccurately that it's even errorneous and misleading. I trcommend to use another book. I'd rdcommend the Berkeley physics course volume on Statistical Physics (the "little Reif").
 
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  • #6
Doc Al said:
Ah, I think I see what you're saying. I can appreciate the confusion.

I would have said something like: A monatomic gas molecule has three degrees of freedom, a diatomic molecule has five, etc. And the equipartition of energy gives the average energy associated with each degree of freedom.
Yes, that makes perfect sense; I mean the last paragraph.

It appears that degree of freedom means the independent coordinate/variable/term.
 
  • #7
vanhees71 said:
For me the excerpt from the book is formulated so inaccurately that it's even errorneous and misleading. I trcommend to use another book. I'd rdcommend the Berkeley physics course volume on Statistical Physics (the "little Reif").
I agree. Its clearly confusing since a student reading these paragraphs from that book would be left wondering "What exactly is a degree of freedom".
 
  • #8
The correct statement for the equipartition theorem is that any phase-space-degree of freedom, which enters the Hamiltonian quadratically (!!!) contributes ##k_{\text{B}} T/2## per particle to the (mean) energy. E.g., for an ideal mon-atomic gas, the single-particle Hamiltonian is ##H=\vec{p}^2/(2m)##, and thus the mean energy per particle is ##3 k_{\text{B}} T/2##. For two-atomic (and more-atomic) molecules you have two (three) more rotational degrees of freedom. This is when the vibrational modes are still frozen, i.e., at not too high temperatures. At higher temperatures you get additional vibrational degrees of freedom and the corresponding contributions to the mean energy per particle (in the harmoni-oscillator approximation).
 
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FAQ: Conflicting definition of degree of freedom in Kinetic Theory of Gases

What is the degree of freedom in the context of the kinetic theory of gases?

The degree of freedom in the kinetic theory of gases refers to the number of independent ways in which a gas molecule can move or store energy. For a monoatomic gas, this typically includes three translational degrees of freedom, corresponding to movement along the x, y, and z axes. Diatomic and polyatomic gases can have additional rotational and vibrational degrees of freedom.

Why is there a conflict in the definition of degrees of freedom for diatomic gases?

The conflict arises because the degrees of freedom for diatomic gases can vary depending on the temperature. At lower temperatures, only translational and rotational degrees of freedom are active, while at higher temperatures, vibrational modes become significant. This leads to different interpretations and calculations of specific heat capacities and other thermodynamic properties.

How do vibrational modes affect the degrees of freedom in diatomic gases?

Vibrational modes add additional degrees of freedom to diatomic gases. Each vibrational mode contributes two degrees of freedom (one for kinetic energy and one for potential energy). However, these modes are typically only excited at higher temperatures, which can complicate the calculation of thermodynamic properties.

What are the implications of different degrees of freedom on specific heat capacities?

The specific heat capacity of a gas is directly related to its degrees of freedom. For monoatomic gases, the specific heat capacity at constant volume (Cv) is (3/2)R. For diatomic gases, it can be (5/2)R if only translational and rotational modes are considered, but it increases if vibrational modes are also excited. This variation can lead to discrepancies in theoretical and experimental values.

How do experimental observations reconcile with the conflicting definitions of degrees of freedom?

Experimental observations often show that the specific heat capacities of gases vary with temperature, which supports the idea that different degrees of freedom become active at different temperatures. By measuring specific heat capacities at various temperatures, scientists can determine which degrees of freedom are significant and reconcile the theoretical models with experimental data.

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