22 July 2017

Rising mist(s)

Another of my comments written on the '67 calendar:


Okay, only one or two more, plus some actual appointments written on the calendar, later.

18 June 2017

Leave it to beaver

On second thought, anybody who's needed to get a cat into a pet carrier knows the unlikelihood of a cat going to sleep inside a darkened box.  Not to mention the unlikelihood of even getting the cat in the box.  The cat would more probably knock over the intended experimental equipment and yowl until you let him or her out.  And who could blame 'em?  Was old uncle Erwin--old (40s) compared to Heisenberg and Dirac (20s)--making a subtle joke by suggesting doing the experiment with a cat?  Was he thinking that since the mouse is usually the poor creature who gets inhumanely put in a humanly concocted experiment that he'd use it's opposite, a cat?  Or was there a cat asleep on his desk when he thought up the experiment?

Whatever the case may be, the next 1967 calendar animal I put words in the mouth of was a beaver:



No, I wasn't very good at spelling as a 12 and 13 year old kid.   I got better.

17 June 2017

Sleeping cat?

In 1998, when I was taking an undergraduate quantum physics class taught by Steven Weinberg at UT-Austin (a rare thing for him to teach an undergrad course--he gave us only homework sets and no exams, which I very much liked), the book for the course was Intro to Quantum Mechanics, by David J. Griffiths.  Yep, the one I mentioned earlier, with a drawing of a live cat on the front and a dead cat on the back.  When the 10-year-old daughter of my girlfriend at the time saw the book she called the cat on the back a "sleeping cat."  I told her that it was actually supposed to be a dead cat, according to the Schrodinger thought experiment that was represented by the two drawings.

Now I'm thinking why not let the cat have a 50% chance of being awake or asleep? Have the experiment use a sleeping potion released in the sealed box with the cat instead of cyanide gas.

Well, the problem with that is the cat could enter this state, the state of being asleep, independently of what the experimental apparatus does.  Who could blame the cat in a dark closed box for going to sleep?  But this possibility would mess up the 2-state probability transferance from atomic system (metastable quantum state) to the cat.

But, on the other hand, the cat could also enter the state of being dead independently!  If you put it in a sealed box, it's not gonna live too long without air being pumped in! Or it could have a heart attack or whatever, and this possibility is ignored by usual discussions of the "cat paradox."

So when I get around to actually discussing the significance of Schrodinger's cat, I'll use a sleeping cat versus an awake cat and see how that works out...

Three semesters after I took the Weinberg quantum course, I took yet another undergraduate quantum mechanics class, this time at the University of South Carolina, and it even used the same book.  However, it was a traditional class. Exams, including a final exam, were given.  I'd made an "A" in Weinberg's difficult-homework-based class.  Using the same book in a standard homework-and-exam-based class a year and a half later--with actually a very good teacher (Weinberg was okay, but taught like he was giving one of his research seminars--lecturing, with little if any class participation encouraged)--I made a "B".

28 May 2017

More '67 calendar "jokes"

I mentioned watching "Get Smart" as a kid back in old '67, which, by the way, was the year J. Robert Oppenheimer died at age 62, on February 18th, my parents' 25th wedding anniversary, but I certainly did also watch "F-Troop."  If I remember correctly, I wanted to be a comedian when I grew up. Thus the comments I made on some of the animal drawings in the IP "Executive Desk Calendar," of which here are two more.

07 May 2017

1967 Calendar

I was in the seventh and eighth grades in 1967.  I got a set of drums, a trap set, from my parents, after having received a snare drum for Christmas in 1966.  The condition under which I received the trap set, which was a used Slingerland set (black), was that I would join the Dial Jr. High band in the eighth grade.  Playing in the band would have been an embarrassment for me.  Not cool. I fortunately didn't have to play with the band in public, due to the fact that I was a beginner.  I was in the "training band," and recall spending quite a bit of the class period alone with the two other drummers in a practice room, shooting the breeze and not practicing. 

Also I remember getting sent to the principal's office for putting up a photo from Playboy in the bandroom window.  The older guy among us three training drummers brought it to school.  Not the only time I got sent to the principal's office that year, but the only band-period principal's office trip I can remember.

The credits at the end of A Serious Man say copyrighted material from Playboy was used with permission of the magazine, but I've looked for and haven't seen any Playboy material in the movie. It's most likely shown on the wall in the blurry background of the scene where Danny is practicing for "the Torah portion" (singing) of his bar mitzvah.  Nope it’s in the scenes where Danny and his profane friend pick the lock on Rabbi Turchek's desk drawer: the particular shot shows the drawer being closed, and lasts only about half a second. Instead of the contents of the drawer that Danny and his friend are shown rummaging through looking for Danny's transistor radio (and the $20 bill stuck in the faux leather case), the quick-shot of the closing drawer's contents shows different stuff, including a Playboy magazine.

I rediscovered a few years ago an International Paper Co. 1967 desk calendar that was kept on the desk in my parents bedroom that year: 


I wrote comical comments in it ("Get Smart" was one of my favorite shows)...



... more of which will be on display later.  In Rabbi Scott's office in the movie ("Things aren't so bad.  Look at the parking lot, Larry! Just look at that parking lot."), a calendar for May and June 1967 is shown, so I'm starting with May.

07 March 2017

Planck oscillator average energy Part II

See the last part of my previous post for equations leading up to here. Leaving out the constant C for the moment, and using the total rather than the partial derivative, since Uυ  is the only independent variable,
dSυ / dUυ  =   (1/ε)log [(1 + Uυ / ε)] + ( 1/ε)(1+ Uυ / ε)/ (1+ Uυ / ε)
                                                           - (1/ε)log (Uυ / ε) - (Uυ /ε)(1/ε)(1/Uυ )
The red factors cancel, giving
dSυ / dUυ = (1/ε)log [(1 + Uυ / ε)] + (1/ε) — (1/ε)log (Uυ / ε) — (1/ε),
where the red terms now cancel. With C reinserted, and dSυ / dUυ replaced with 1/T, the result is
1/T = C{(1/ε)log [(1 + Uυ / ε)] — (1/ε)log (Uυ / ε)} 
             = (C/ε){(log [(1 + Uυ / ε)] — log (Uυ / ε)} = (C/ε){(log [(1 + Uυ / ε) / (Uυ / ε)]}
or                                        ε /CT = log[(1 + Uυ / ε) / (Uυ / ε)].


Taking exponentials of both sides
exp(ε /CT ) = (1 + Uυ / ε) / (Uυ / ε)
= 1 / (Uυ / ε)  +  (Uυ / ε) / (Uυ / ε)
=  ε / Uυ   +  1
We want an expression for the average oscillator energy Uυ , so some more algebra is required, namely,
ε/Uυ = exp(ε /CT )  –  1,


 or                                                      Uυ = ε /[ exp(ε /CT ) – 1].

This was Planck's new expression for the average energy of a resonator in equilibrium with black-body radiation—new as of 1900. There's a lot more to discuss here: 1. why Planck's constant h and Boltzmann's constant k come out of this calculation,  2. the Rayleigh-Jeans and Wien limits at the low end and high end, respectively, of the black-body frequency spectrum, 3. the Wien displacement law, 4. the "wrong" assumption of indistinguishable energy elements Planck made when he chose the permutation calculation that goes into finding the entropy, and 5. the choice of perfectly reflecting (mirror) walls versus perfectly absorbing (black) walls of the cavity. For mirror walls there is absorption with immediate re-emission, while black walls would absorb and only re-emit after affecting the motions of the atoms of the material, right? Sure! But just in case, check with Born & Wolf or Hecht &Zajac if you want to be further enlightened.
On this last question, Sommerfeld, in his Thermodynamics & Statistical Mechanics book, Section 20, says that when the walls are perfectly reflecting, they cannot come into temperature equilibrium with the radiation, and a “speck of soot” must be introduced into the cavity as a “catalyzer” to achieve equilibrium!  And there's also the question of where the oscillators (resonators) are, exactly. Are they supposed to be in the cavity walls or are they imaginary particles, like soot, floating about in the air in the cavity? Apparently, with black walls, the resonators are in the walls, and with mirror walls, the resonators need to be free-floating in the air of the cavity. In calculations, we sort of assume a vacuum cavity, so that the speed of light = c = γυ can be used in the equations rather than c/n, where n is the index of refraction of the (heated) air in the cavity. For air (at 300 K) n ≈ 1.0003, so we won’t worry about that right now.


Right now we will look at Einstein's 1907 calculation using geometric series to find Planck's expression for the average energy of a simple harmonic oscillator system. Einstein says, "To arrive at Planck's theory of black-body radiation ... one assumes Maxwell's theory of electricity yields the correct relationship between radiation density and Ē.”  Yes, Einstein uses Ē instead of Uυ for the average resonator energy. The “correct relationship” he’s referring to is Planck's "simple relation," uυdυ = (8πυ2/c3)Uυ dυ, where Uυ is average resonator energy, as discussed in the last part of my Walking further with Planck post.
On the other hand,” Einstein continues, “one abandons equation (4),

Ē =  ʃE exp [(-N/RT)E]dE / ʃ exp [(-N/RT)E]dE  = RT/N = kT,


i.e., one assumes that it is the application of the molecular-kinetic theory which causes a conflict with experience. ... this stipulation involves the assumption that the energy of the elementary structure under consideration assumes only values infinitesimally close to 0, ε, 2ε, etc."


Einstein doesn't bother to show the actual equation (4) calculation, but I guess it was a routine calculation by that time. One way it can be done is by separately finding the average potential energy and the average kinetic energy of a one-dimensional harmonic oscillator. Then the E in the integrals in the expression above is, respectively, a constant times x-squared or a different constant times p-squared. The result of the integration in each case is kT/2.  Try it!  Adding the potential and kinetic contributions together gives kT.  This is the classical result, which Rayleigh (with a numerical correction made later by Jeans) calculated in 1900.

Page 216 of the Einstein paper shows this result. Page 217 shows the series representation that gives Planck's result. Einstein was apparently the first to obtain Planck's result using the infinite series calculation. Nowadays this is how most introductory textbooks do it, although they use discrete sums instead of the integral notation used by Einstein.

I will show the calculation as done by Koichi Shimoda on page 70 of Introduction to Laser Physics.  We now have E = nhυ, and use Uυ again instead of Ē (if the Greek letter nu comes out as u, I'll try to fix that later...)

Uυ =  Σ nhυ·exp(-nhυ/kT) / Σ exp(-nhυ/kT)

where the sums are over n = 0 to n = ∞. This is Boltzmann’s method for calculating a statistical average, but with discrete sums instead of integrals because we have discrete or quantized energy levels.  Shimoda lets exp(-hυ/kT) = r in order to make it clear that the denominator is the geometric series

Σ exp(-nhυ/kT)  =  Σ rn  = 1/(1-r) =1/[1- exp(-hυ/kT)].

And he writes the numerator as 

Σ nhυ·exp(-nhυ/kT) = hυ Σn rn

then use the derivative of rn
drn/dr  =  nrn-1

and compensates for the n-1 exponent by using an extra factor of r out front when writing the sum:


Σn rn  = rΣ drn/dr  = r (d/dr )Σ rn ,


since a sum of derivatives is the derivative of the sum.  Now we put in 1/(1-r) for the geometric series sum, and do the derivative

r (d /dr) (1-r)-1 =  r(-1)(-1)(1-r)-2  =  r/(1-r)2.

Putting the closed-form expressions for numerator and denominator into the equation for average energy gives

Uυ = hυ[r/(1-r)2] / [1/(1-r)]  = hυr(1-r) / (1-r)2 = hυr / (1-r),
and using the trick of pulling out a factor of r in the denominator gives
hυr / (1-r)  = hυr / [r( 1/r – 1 )]  =  hυ ( 1/r – 1 )-1.

Now 1/r is replaced by exp(hυ/kT), and the Planck expression for average energy is the result:


Uυ  hυ / [exp(hυ/kT) – 1]

One overall final point about the average energy:  It is also given by the expression we used in calculating the entropy of an oscillator.  Remember that?  It’s just the arithmetic mean, E/N, where E is the total energy of N oscillators.  Planck specified that the energy E is partitioned among P elements, each with energy ε, so the average energy is


Uυ  =  E/N = Pε/N.


This simple average must equal the thermodynamic expression Planck found for average energy:


/N  = ε /[ exp(ε /CT ) – 1],


or                                                       P/N   =  1/[ exp(ε /CT ) – 1].

This is sort of self-explanatory, but not quite. Planck has already said that these N resonators have a common frequency υ. (Whatever happened to the other N’, N’’, … resonators with frequencies υ’, υ’’, … and energies E’, E’’, … ? I don’t know!  I’m hoping to get back to that. November 2017:  Planck does discuss the other resonators, see my 31 Oct 2017 post.)  If we go ahead and use ε = hυ, then P/N could be called the occupation number associated with the frequency υ.   In modern terminology, it is the Planck thermal excitation function,


<n>  =  1/[ exp(hυ/ kBT) – 1],


giving the  mean  number of photons excited in the field mode at temperature T.


To be discussed later:  Why did Planck choose a direct proportionality between energy and frequency? At what point does the quantization of energy occur? (The proportionality between energy and frequency is not in itself quantization.)  How did Planck find the constants h and k? And the biggest question, how can all this be explained—that a continuous oscillator can have discrete energy levels—or as Einstein put it, what is the "mechanism of energy transfer"?  In classical physics the mechanism is acceleration, caused by a net force acting on an electric charge. So far, there is no mechanism in quantum theory to explain how charges radiate, in spite of the potential energy appearing in the Schrödinger equation. There are only acausal calculational tools, such as transition probabilities and the use of time-dependent perturbation theory, as in the Feynman diagrammatic perturbation approach (well, okay, only for unbound energy states, so we’ll just come back to all that later).  



20 February 2017

Grad Student Newsletter UT-Austin 20 Feb 1967


Sorry, the copy I have of this newsletter was cut off at this point. I found it in a paperback book of Enrico Fermi's Lecture Notes on Quantum Mechanics that I got from David Potter of Austin, who was a physics grad student at UT-Austin in 1967.  I arrived as a grad physics student there a little over 20 years later.  See my journal entry from 30 August 1987 about grad student orientation, posted on 30 August 2017.