Sorry about sending the duplicate uncommented post! Just a sign of my increasing senility.

On Aug 8, 2007, at 2:54 PM, Michel Jullian wrote:


----- Original Message -----
From: "Horace Heffner" <[EMAIL PROTECTED]>
Sent: Wednesday, August 08, 2007 10:18 PM
...
I certainly don't agree it is necessarily the field that counts in
Fig. 1 when it comes to electron fugacity. Referring to Fig. 1
again,  if the "++" electrode is at +1,000,000 V and the "x"
electrode is at +980,000 V, the electron fugacity in the X electrode
will be reduced from what it would be if  the "++" electrode were at
-1,000,000 V and the "x" electrode is at -1,020,00 V.

Not so, but at least our controversy is now clearly stated. If you have two facing plates (= a capacitor) with a power supply maintaining a 20kV difference of potential between them as is the case in the two configurations you discuss, then whatever their potential wrt ground,


It doesn't matter to what the voltage is relative. There are 4 potentials involved: +1,000,000 V +980,000 V, -1,000,000 V -1,020,00 V. The surface electron fugacity is necessarily higher at the most negative potential, -1,020,00 V. However, in earlier discussions I think I defined the potentials I used as being with respect to ground where ground was defined as a body having balanced plus and minus charges. This is consistent with a fugacity of 0 being defined as being at a potential 0, at least with respect to the above surfaces. I don't think there is a correlation of fugacity to potential with regard to matter inside a conductor. This might all be a fairly moot point inside a Faraday cage, from a practical point of view.



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On Jul 31, 2007, at 10:22 AM, Horace Heffner wrote:
On Jul 31, 2007, at 12:21 AM, Michel Jullian wrote:


A few comments on this:

1/ You mean extremely negatively charged I imagine, an extremely
negative electric potential being meaningless if you don't say
relative to what.


This is where the term "electron fugacity" instead of "potential" has
usefulness.  I mean relative to the potential of any material having
a neutral charge balance, one positive for every negative charge. In
practical terms this means ground.

************* Note the above definition. *************



What do you mean? If you're saying that an object at ground potential is necessarily neutral, or close to neutral, you couldn't be more wrong.

I realize that ground (earth) potential varies a great deal, both to the positive and to the negative, due to weather and solar wind effects. This is why I said below that "ground electron fugacity varies a great deal". This may in fact account for the "Salt Lake City effect" and why CF cells that work at high altitude low storm frequency places don't work for Scott Little in Texas. 8^) However, I would expect that *typically*, setting the cathode potential to -20 KeV or more would make for a high surface electron fugacity.
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assuming that's what you mean by "at so many volts", the excess charges at the facing surfaces will be _exactly_ the same.


But that is just it. I'm not talking about *relative* "excess charges". I'm talking about electron fugacity, talking about the importance of obtaining excess electrons over positive charges. I'm talking about electron fugacity as defined by the energy cost to move an electron from infinity (defined as infinitely far away from all charge), or ground (as defined above), to the surface of interest (also assuming no surfaces past through in between.) It's all about an absolute number of excess electrons over positive charge.

In my article I footnote fugacity to:

http://www.mtaonline.net/~hheffner/DeflationFusion.pdf

which states:

"In statistical mechanics, the fugacity is one of the parameters that define the grand canonical ensemble (a system that may exchange particles with the environment). It represents the effort of adding an additional particle to the system."

I guess I should spend more time in the article defining terms, especially "electron fugacity". I thought it was very clear but on reading I can see it is not actually well defined within the article itself except maybe via footnote. Maybe I should even use a different term to clear up any confusion, like "excess electron density". (See below.)


In a capacitor, excess charge on each plate = capacitance times voltage difference between the plates, q = C*Delta_V, as you know. Can you see any dependence on absolute voltage in the formula?

No, and that is appropriate. The above formula is related only to potential and not related to electron fugacity.



You see, potential is only defined by its derivative (or gradient), the field, so as in any integral you can add any constant you please to it it won't change a thing. Absolute value of potential is totally meaningless, it doesn't have one in fact.


I think it does within my definition of fugacity because that definition establishes the meaning of 0 potential for a conductor surface.


Only differences of potential matter. Controversy solved?

Michel


Not yet! But thanks for trying. My concepts are certainly not clear yet - even in my own head, which is usually a bit foggy anyway.

It is interesting that well inside a conductor without a current you might think things should be neutral because it is a conductor. There should be no "electron excess" or "electron deficit" because the potential is everywhere the same. However, if a strong electric field goes through that conductor then charges realign to neutralize that field. If the conductor was neutral to begin with, i.e. had exactly 0 "electron excess", then one part of the conductor will have an electron excess, and one part will have an electron deficit. Similar things happen in electrolytes in strong electrostatic fields. This change in electron deficit value, what I was calling electron fugacity, imposed throughout the Szpak electrodes and electrolyte, I think had dramatic effects on the morphology of the Szpak electrodes.

I think it may be useful to define the term rho_e to mean "excess electron density" such that if a volume V of matter has N+ positive charges and N- electrons then:

   rho_e = q(N- - N+)/(V (N- + N+))

and the SI units for it would be Coul/m^3, but might seem more meaningful in excess electron charge per cubic angstrom units. Note rho_e can be positive or negative and there is no need to talk about electron excess or electron deficit.

Of related interest is that in the case of a current through a CaO barrier within a fully loaded PD matrix a rho_e gradient can develop to either side of the barrier because fully loaded Pd is not really a full fledged conductor, and because a field develops through the barrier, and near the barrier, because the barrier tunnels nuclei and electrons with differing probabilities.


Horace Heffner
http://www.mtaonline.net/~hheffner/



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