Sunday, June 29, 2014

My Note 1) Planck's Radiation Law

My Note 1) Planck's Radiation Law

The original Note 25) is "Classic Radiation Theory and Planck" introduces

1. Stefan–Boltzmann Law
2. Wien's Displacement law
3. Vien's Radiation Law 
4. Rayleigh–Jeans Law
5. Planck's Radiation Law

Planck's Radiation Law or simply Planck's Law is a big issue so it is better to check the originals.

List of references in Wiki " Planck's Law" (08-Aept-2012)

Very useful articles

1) http://bado-shanai.net/map%20of%20physics/mopPlancksderivBRL.htm
2) Great Experiments in Physics: Firsthand Accounts from Galileo to Einstein. edited by Morris H. Shamos
3) http://publishing.cdlib.org/ucpressebooks/view?docId=ft4t1nb2gv&chunk.id=d0e391&toc.depth=1&toc.id=d0e391&brand=ucpress
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The following part is emphasized by Planck himself (the underlined part) so this part is surely important.

From  "On an Improvement of Wien's Equation for the Spectrum"  (1900) as well as "On the Law of Distribution of Energy in the Normal Spectrum" (1901).

From "On the Law of Distribution of Energy in the Normal Spectrum"

"
To answer this question we first of all consider the vibrations of the resonators and assign to them arbitrary definite energies, for instance, an energy E to the N resonators v , E' to the N' resonators v', . . . . The sum
E + E' + E'' + . . . = E0
must, of course, be less than Et. The remainder Et −E0 pertains then to the radiation present in the medium. We must now give the distribution of the energy over the separate resonators of each group, first of all the distribution of the energy E over the N resonators of frequency v . If E considered to be continuously divisible quantity, this distribution is possible in infinitely many ways. We consider, however – this is the most essential point of the whole calculation – E to be composed of a very definite number of equal parts and use thereto the constant of nature h = 6.55×10−27 erg · sec. This constant multiplied by the common frequency v of the resonators gives us the energy element " in erg, and dividing E by " we get the number P of energy elements which must be divided over the N resonators. If the ratio is not an integer, we take for P an integer in the neighbourhood.

"
1) Distribution 

Planck did not emphasize but he did "grouping" which is actually the process of making "continuously divisible quantity" to "discontinuous divisible quantity". For instance, when you make a distribution chart of the following simple data from the measurement "grouping" is required. Otherwise you cannot find distribution of the data.

The lengths of 10 pencils selected as samples from those shipped from a relatively good pencil factory (specified length 190.50mm +/-2.0mm)

Pencil No. 1     189.73
Pencil No. 2     190.06
Pencil No. 3     191.29
Pencil No. 4     191.14
Pencil No. 5     190.68
Pencil No. 6     190.95
Pencil No. 7     189.87
Pencil No. 8     190.48
Pencil No. 9     190.24
Pencil No. 10   190.55

If you do not do "grouping" the number of each pencil length is 1 so the chance for each number is 1/10. We cannot see "distribution" except "1/10". If you do "grouping",  you can find the number for each group.

Group 6) 189.00 - 189.49  -   0pc       Chance or distribution 0%
Group 1) 189.50 - 189.99  -   2pc       Chance or distribution 20%
Group 2) 190.00 - 190.49  -   3pc       Chance or distribution 30%
Group 3) 190.50 - 190.99  -   3pcs     Chance or distribution 30%
Group 4) 191.00 - 191.49  -   2pcs     Chance or distribution 20%
Group 5) 191.50 - 191.99  -   0pcs     Chance or distribution 0%


The "grouping" unit is 0.50mm.

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2) "permutations" and "complexions"

Planck says in  "On an Improvement of Wien's Equation for the Spectrum"  (1900)

"
From the theory of permutations we get for the number of all possible complexions


N(N + 1) · (N + 2) . . . (N + P − 1)       (N + P − 1)!
------------------------------------- =  --------------
       1 · 2 · 3 . . . P                                 (N − 1)!P!

or to a sufficient approximations,


       (N + P)N+P
  =  -----------
       NNPP


"
a) Planck uses "permutations" and "complexions" . But the first part can be gotten by using the following more simple "combination" formula






 In the Planck's case n = N + P,  r = P


b) No explanation on the approximation here. Planck kindly added the following between the above two formulas in in his "On the Law of Distribution of Energy in the Normal Spectrum". (1901)


"
Now according to Stirling’s theorem, we have in the first approximation:

N! = NN

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3) Planck's Resonators

There is no his explanation on the Resonators he repeated mentioned. So to understand what he says we need some background. The following is a part of the background. From:3) http://publishing.cdlib.org/ucpressebooks/view?docId=ft4t1nb2gv&chunk.id=d0e391&toc.depth=1&toc.id=d0e391&brand=ucpress

"
Planck's Resonators
The empirical validity of Kirchhoff's law, Stefan's law, and Wien's displacement law left no doubt about the legitimacy of combining electrodynamic and thermodynamic laws; and Planck was well aware of these developments. In 1895 he decided to examine the electrodynamic mechanisms responsible for the thermalization of radiation, hoping to find in them the ultimate source of irreversibility and to perhaps determine the arbitrary function in Wien's displacement law. This grand program focused on a very simple system, a Hertz resonator: that is, a small, nonresistive, oscillating electric circuit interacting with electromagnetic waves, the characteristic wavelength of the oscillator being much larger than the oscillator. The simplest choice was considered the most adequate by Planck,

30
Figure 6.
Planck's intuition of the source of thermodynamic
 irreversibility: the diffusion of a plane electromagnetic
wave by a resonator (at the frequency of the wave).
 
for in light of Kirchhoff's theorem, the properties of thermal radiation could not depend on the specific properties of the thermalizing system.[43]
What first attracted Planck's attention was the apparent irreversibility of the interaction between radiation and resonator: a plane monochromatic wave falling upon a resonator forces vibrations of the resonator when the condition of resonance is approximately met; in turn these vibrations emit secondary waves over a wide angle (fig. 6). Also, an excited resonator left to itself emits radiation at its characteristic frequency and thereby gradually loses its energy. Such processes, resonant scattering or radiation damping, looked essentially irreversible, even though the total energy (that of the resonator plus that of radiation) was strictly conserved (in the absence of the Joule effect in the circuit). Planck concluded:
The study of conservative damping seems to me highly important, because it opens a new perspective on the possibility of a general explanation of irreversible processes through conservative interactions, a more and more pressing problem in contemporary theoretical physics.[44]
These results of classical electrodynamics are now very well known; they are usually obtained through a specific model of the resonator, for instance an elastically bound electron. In 1895, however, the existence of the electron had not been proved; and Lorentz's formulation of electrodynamics, with its detailed analysis of microscopic sources, was not yet currently known (the famous Versuch was published in the same year).

31
Planck was therefore confined to a different method, first used by Hertz in 1889 for a calculation of the energy radiated by an oscillating dipole. In this method the detailed structure of the resonator was irrelevant .[45]
As we shall observe in the following, Planck maintained this generality throughout his program and even gave it an essential role. It is therefore useful at this point to explain how the equation of a resonator in an electromagnetic field can be established with this method. Another reason for analyzing Planck's reasoning is that it is typical of a style of theoretical physics, namely, concentrating on the features of physical systems which can be determined on the basis of general principles only, without recourse to detailed microscopic assumptions. Nevertheless, hurried readers may be content with these general comments and may jump to the equation (62), p. 36, for the evolution of the dipolar moment f of a resonator.

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