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Re: microwave, RF heating



At 01:44 PM 5/29/00 -0500, brian whatcott wrote:
The ruling explanation for [at least one kind of] microwave absorption
is bond rotation - rather than molecular 'hand clapping' or stretching.
Can one on prior principle, deduce if bond rotation is hindered in
a crystal lattice, I ask myself?

At 02:37 PM 5/29/00 -0500, Doug Craigen wrote:
Microwave absorption spectral lines are mainly due to molecular
rotation not vibrations (the latter are IR) and are typically 20-30
GHz. The microwave oven (2.5 GHz) is far below this - but the spectra
lines are very smeared due to neighbor interactions so I can imagine
that there is
weak absorption due to rotations at 2.5 GHz. Weak absorption is what we
require so that the microwaves penetrate deeply. It would be hard to
cook food if exciting with a frequency near a spectral line.


I agree that we need to consider the effect of far-far-far off-resonance
transitions. This dovetails nicely with last week's thread: all spectra
are continuous; tails matter.

Let's knock some numbers together.
I = moment of inertia
I = integral of r^2 dm, where r is distance and m is mass
L = angular momentum = omega I
L is quantized in units of hbar
hence
I = hbar / 2 pi f, where f = frequency
and the challenge is to find I big enough so that f can be as small as 20
GHz. This is just sorta almost possible if you imagine a hydrogen-bonded
H2O:OH complex where the oxygens are rotating around a common center,
separated by a few angstroms. Maybe.

The rotation of such a critter would be greatly hindered by the crystal
lattice. It would be pretty dodgy in the liquid, I suspect.

I'm not sure I 100% believe this picture, but the numbers are close enough
to reasonable that perhaps a refinement of this picture can be
found. Water is funny stuff.

Such a picture (rotating complexes) predicts that the RF absorption should
have all sorts of strange dependence on temperature, density, dilution with
alcohol, et cetera. The plot thickens!