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So in this answer:

Folks figured out thermodynamics before statistical mechanics. In particular, we had thermometers. People measured the "hotness" of stuff by looking at the height of a liquid in a thermometer. The height of a thermometer reading was the definition of temperature; no relation to energy.

What happens, if I invoke collision dynamics from Chapman–Enskog theory? And measure the mass diffusivity (along with every other variable) to measure the temperature?

$$D = \frac{AT^{3/2}}{p \sigma^2_{12} \Omega} \sqrt{1/M_1 + 1/M_2} \tag{1}$$

where $D$ is the diffusion coefficient ($cm^2/s$), $A$ is an empirical coefficient equal to $1.859 × 10^{-3} \frac{{A}^{2}\cdot {cm}^{2}}{K^{3/2}\cdot s}$, index the two kinds of molecules present in the gaseous mixture, $T$ is the absolute temperature ($K$), $M$ is the molar mass (g/mol), p is the pressure (atm), $\sigma_{12} $ but usually of order $1$ and is the average collision diameter and $\Omega$ is the collision integral. (See here for the equation)

I suspect this argument now automatically fails:

[a] Note that if temperature had dimensions of energy then under this definition entropy would have been dimensionless (as it "should" be).
[c] Note again how $k_b$ and $T$ show up together.

More explicitly if I follow the prescription where $x \to p D$:

$$ L(p D) = \ln (\Omega) + T(E_0 - E(p D)) \tag{2}$$

we see an implicit assumption is present that the product of mass diffusivity and pressure must be a function of energy (I've never heard of this noether invariant of time translational invariance). This is not true and has to be shown valid in this case! (if not every).

In fact I will go further and prove it cannot be the case heuristically. Using Fick's law (which is a step down from Chapman's collisional dynamics)*:

$$ S = \int \sum_i \frac{{p_i }^2}{2m} dt \approx \frac{N}{2} m \bar{v} l \propto D \tag{3}$$

where $S$ is the action, $p_i$ is the momentum, $m$ is mass, $N$ is number of particles, $\bar{v}$ is the average velocity and $l$ is the mean free path. Also $ D = \bar{v} l $ There is no mention of pressure above.

Does Chapman–Enskog theory provide a way to measure temperature independent of energy? Is this answer still valid?

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    The temperature is related to the mean kinetic energy of the gas molecules, and I'm sure there are some factors of $k_B$ hiding in some of the coefficients here. Also, what are $\sigma_{12}$ and $\Omega$? – d_b Feb 08 '23 at 22:37
  • See Eq. 2.6 of the following PhD thesis: https://thesis.library.caltech.edu/1586/ I believe it is related or even equivalent to your expression for $D$ from Wikipedia. You will see the factors of $k_B$ are more explicit. I have tried to track down this equation in the Chapman and Cowling book for more detail without luck, but I'd suggesting searching there if you want more detail. It is a comprehensive text to say the least. – d_b Feb 08 '23 at 23:25
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    The answer to this question is simply that $A$ has explicit Kelvin in it. – DanielSank Feb 09 '23 at 01:07
  • @DanielSank I've edited the question to show that you have an implicit assumption (which is not satisfied in this case) – More Anonymous Feb 09 '23 at 05:52
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    I think you are on a wrong track... but +1 for tenacity and trying to get to the bottom of it. – Roger V. Feb 09 '23 at 09:30
  • @RogerVadim thank you for your kind words and your answer. I suspect when you say "It is even somewhat illogical to define temperature - which is a property of in equilibrium state" is a response to my equation 2? If so can you point me to a reference? – More Anonymous Feb 09 '23 at 09:35
  • You can take any textbook on statistical physics, and it will define temperature for equilibrium system - either in terms of average kinetic energy or when discussing equilibrium between two bodies, etc. See Wikipedia for the list of approaches. Standard texts are Huang, Reichl, Landau&Livshitz. – Roger V. Feb 09 '23 at 09:41
  • Hydrodynamic approximation itself is derived by assuming local equilibrium and defining the temperature as an equilibrium property of a physically small volume. This is not clearly spelled in the WIkipedia article on CHapman-Enskog, buts ee, e.g., these notes and other references in this answer. – Roger V. Feb 09 '23 at 09:45
  • @RogerVadim I think temperature can be defined in non-equilibrium as well. In chapman one does it by means local equilibrium hypothesis. In which case I don't see how you can use that statement to push back against equation 2? Also, Im assuming your in agreement with the answer i reference? – More Anonymous Feb 09 '23 at 09:49
  • Local equilibrium means that you use the equilibrium definition of temperature. In fact, they plug into kinetic equation an equilibrium distribution, but assume that its parameters (including temperature) slowly vary over space. – Roger V. Feb 09 '23 at 09:52
  • Okay so the takeaway is equation 2 is ill-defined since temperature is a local phenomena but $pD$ is global? If so, can we think of $pD$ locally as well. Honestly I feel there is some non trivial sleight of hand else the claim $f(pD)$ is a time translational invariant(/energy) must be true (at least locally)? – More Anonymous Feb 09 '23 at 10:00
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    I don't want to get into technical details here - perhaps you could ask a question specifically about this equation, and make it less "provocative" - when you ask about temperature it attracts a lot of attention (and votes, perhaps), but it doe snot necessarily attracts people with technical expertise (and there are some people here well-versed in Cahpman-Enskog, see, e.g., this answer and this one). – Roger V. Feb 09 '23 at 10:06

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This question and your other recent question are ultimately about the systems of units (like SI or CGS) and not about temperature. In most systems of units the majority of quantities are expressed in terms of a few basic units, even if sometimes they are given special names like Joules/ergs for energy or Hz for frequency. The number of such basic units may vary - e.g., one does not have to define an independent unit for charge or temperature - and there is actually a price to pay for defining extra basic units - in terms of having to introduce additional constants, like Boltzmann constant $k_B$, vacuum permittivity $\varepsilon_0$ and so on. Moreover, one could even get away with less units than the basic length, mass and time - e.g., in spectroscopy frequency is often measured in inverse centimeters. Sometimes quantities may have rather surprising units when expressed in terms of basic ones - like capacitance in CGS system being measured in centimeters.

Another approach is to define natural units by expressing basic units in terms of basic constants or even by demanding that some or all the basic constants are equal to $1$ (see Planck units.)

Getting closer to the argument given in the OP: here one redefines the temperature in terms of other dimensional quantities - shifting the problem to defining the unites of these quantities. It does give the impression that the unit of temperature is fixed by those of other units... but we could always define a different unit and introduce a dimensional proportionality constant - but such a constant is our arbitrary choice, there is nothing fundamental about it.

Let me also bring up something that was lost in jumping from phenomenological thermodynamics to Chapman-Enskog - the equilibrium statistical physics, which dispenses with the collisions using quite general arguments - the collisions matter for establishing the thermodynamic equilibrium, but they can be neglected in description of this equilibrium, e.g., in terms of canonical/Boltzmann ensemble - the temperature is already present there, and have unambiguously energy units (e.g., defining the average kinetic energy of molecules in a gas, see equipartition theorem and this answer). BBGKY hierarchy, Boltzmann equation, and Chapman-Enskog arise when we try to describe how this equilibrium is achieved. It is even somewhat illogical to define temperature - which is a property of en equilibrium state - in terms of non-equilibrium theory.

Roger V.
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I did not understand all of them, but I will make an ad hoc link:$$D=\bar{v}l=\bar{v}\frac{kT}{\bar{F}}$$ with:$\;\;\bar{F}l_{x}=kT\;\;,\;\;\bar{P}=\frac{N\bar{F}}{l_{y}l_{z}}\;\;,\;\;\bar{P}V=NkT\;\;\;\;$(*)

so :$$D=\frac{ \bar{v} NkT}{\bar{P}S}=\frac{2}{3}\frac{\bar{v}}{\bar{P}S}\bar{E}$$

For the coefficient of self-diffusion, we find in (*) (rations: 46,47,48): $$D\propto \frac{1}{n}\propto \frac{1}{\bar{P}}\;\;\;\;,T=cst$$ $$D\propto T^{3/2}\;\;\;\;,\bar{P}=cst$$

(*) For example in Berkeley physics course, volume V (Statistical physics)

The Tiler
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  • @Tiler to quickly articulate my objection as posed in the question (equation 2). Usually one must define a Lagrangian to find the Norther' time translational invariant. The prescription provides a different way: https://physics.stackexchange.com/questions/231017/is-the-boltzmann-constant-really-that-important/231065#231065 . If my equilibrium parameter variables can be expressed as a function of temperature. Then it is a function of energy. – More Anonymous Feb 15 '23 at 11:00
  • In (**) we can read : " The entropy S is a dimensionless quantity. The definition (9.1) therefore shows that the temperature has the dimensions of energy, and so can be measured in energy units, for example ergs. In ordinary circumstances, however, the erg is too large a quantity, and in practice the temperature is customarily measured in its own units, called degrees Kelvin or simply degrees. The conversion factor between ergs and degrees, i. e. the number of ergs per degree, is called Boltzmann's constant and is usually denoted by..." – The Tiler Feb 15 '23 at 13:23
  • (**) : https://archive.org/details/landau-and-lifshitz-physics-textbooks-series/Vol%205%20-%20Landau%2C%20Lifshitz%20-%20Statistical%20Physics%20Part%201%20%283rd%2C%201980%29/page/35/mode/1up?view=theater and "In all subsequent formulae the temperature will be assumed measured in energy units." – The Tiler Feb 15 '23 at 13:24
  • And also from the definition of entropy in the classical case: $ S=Ln\frac{\Delta p \Delta q }{(2\pi \hbar)^{s}}$, so defined, is a dimensionless quantity . – The Tiler Feb 15 '23 at 14:19
  • My concern is: the equilibrium parameter variables can be expressed as a function of energy. I think this is non-trivial – More Anonymous Feb 15 '23 at 14:31
  • Examples: $T=\frac{\partial E}{\partial S}|{v};,;V=\frac{\partial W}{\partial T}|{S};,;W=E_{0}-E(s);,;P=-\frac{\partial E}{\partial V}|{S}; ,; u=\frac{\partial E}{\partial N}|{S,V}, F=-\frac{\partial E}{\partial r}|_{S}$.....,u :chemical potential – The Tiler Feb 15 '23 at 19:46