-----Original Message-----
From: [email protected] 
In reply to  Bob Higgins's message:

>How it is implicated at a Pd cathode is a mystery

.... It should occasionally be reduced to the atomic Li at the cathode, but
is unlikely to last long enough to plate out. It is a highly reactive metal,
and will readily react with a water molecule. However, should a Lithium atom
both be reduced as a neighbour of a Hydrogen atom at the cathode, then there
is a possibility for the Li to catalyze Hydrino shrinkage in the H (D). 

Robin,

That is close to what I was going to add - since the first ionization of Li
is 5.39 eV and the second is 75.64 eV. 

Together these add up to 81.02 eV. In terms of Rydberg energy - 27.2 eV x 3
= 81.6 eV. Which is a very close fit for lithium, but of course, that last
electron does not come off easily and that is where nickel may come into
play (as opposed to palladium). Palladium has only a low energy fit but
nickel has a unique ionization situation vis-à-vis lithium. 

I'm not sure how this happens in detail but nickel has an IP5 which is
almost identical to the one of lithium - IP2. Perhaps the lithium and the
nickel interact first, leaving lithium with the deep "hole" that otherwise
would not be there at low temperature; and of course, there are objections
to that as well (how does the nickel hole open up at low energy unless it is
already oxidized) ... but... in looking at the long list of f/H catalysts,
since it turns out that there are none, that's right NONE other than nickel
that share this near identity of deep ionization potentials with lithium, I
am struck by that detail. Maybe it is a coincidence.

Somehow, I do think so, in this case - but I am unsure how the mechanics
could work out the way they do - but we do know that nickel oxide has been
reported to be a better catalyst than nickel in certain situations. This
could be one.

In short, this dogbone reactor could be a situation where the Quantum Sphere
nano-nickel oxide would work very well with lithium to promote deep
fractionalization, following which the f/H then further reacts.

Jones

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