From: Orionworks - Steven Vincent Johnson 

 

Mills recently had more uncomplimentary things to say about recent LENR
research. See SCP thread: "a mixture of nickel and lithium aluminum hydride"
See thread:

 

https://groups.yahoo.com/neo/groups/SocietyforClassicalPhysics/conversations
/topics/4274

 

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Mills is probably correct about his large contribution to the field - but
sadly misinformed about the limits of his patent coverage. He apparently
still believes that he can patent a theory. His patents do not anticipate
the high temperature ceramic reactor, nor do they anticipate SPP, nor the
key feature of near-phase-change in Li-Al alloy. Yes - he deserve more
credit for his insight than he gets, but he should acknowledge that his
actual devices have been one failure after another – going back 20 years. 

 

This inability to take a useful theory from Lab to market is hard to fathom
– but the reality of having nothing to demonstrate, which can be
independently verified - is one reason why Mills is routinely ignored by
peers… well … he is arrogant enough to think he has no peers, but that is
part of the problem, isn’t it? 

 

The interest in lithium  as either reactant or catalyst has been jolted by
the Parkhomov report, which if anything appears to be much more convincing
than the Levi report on which it was based. Not to mention – far more
convincing than the madly sparking seam welder, LOL. Yet… the Russian
results do look closer to the f/H (fractional hydrogen) reaction than
anything nuclear.

 

OTOH, this reaction is not what BLP wishes that they had covered in IP.
Close, but mention of one catalyst is not close enough when half the
periodic table qualitied under your theory. The probative question is - how
does aluminum facilitate access to the deep Rydberg ionization potential of
lithium, in a way which has been missed by everyone including Mills? 

 

First, we can note that after the hydrogen is released from LiAlH4, the
lithium remains alloyed to aluminum, since there is no intrinsic mechanism
to separate the metals below the Li boiling point of 1342 °C which is
closely approached, and this is notably where maximum COP occurs for
Parkhomov.  In an alloy, lithium atoms near the boiling point would react
differently than as an element. “Near-phase-change” could be the key to the
exotherm and to promoting double ionization of Li.

 

To back up a bit – as far back as the early nineties, lithium was claimed to
be responsible for most of the energy gain in electrolytic reactions, since
as an doubly positive ion, Li has the characteristic energy “hole” define by
Mills for promoting ground state redundancy. The first IP is 5.4 eV and the
second is 75.64 eV and together, they present a deficit which is very close
to the value of (3 x 27.2 = 81.6 eV). Nickel provides two more “holes” so
the net reaction being demonstrated both here and for 25 years does fit into
Mills’ model superficially. Yet achieving the ~76 eV to create the “hole” is
almost out of the question for electrolysis in terms of probability and even
at 1300 degrees it would be rare. Yet this can happen readily during
energetic phase change (as Parkhomov has apparently demonstrated).

 

Going beyond Mills - the interatomic spacing for Al-Li alloy is unique at
3.2 Angstrom which is far closer than the crystal spacing in either pure
lithium or aluminum or any other alloy of the two, indicating a high order
of structure – but only in the 1:1 alloy. Therefore the phase change for
“boil-off” of lithium would be expected to be extraordinarily energetic – in
the sense of recalescence and promoting double ionization. Recalescence is a
temporary increase in power, sometimes extreme, which occurs when molten
metal goes through phase-change on cooling. The “near boil-off” of the
double positive ion would expose Li++ to hydrogen gas, even without complete
boil-off. Plus, the phase change can be strongly exothermic even without
ground state redundancy; but… not net gainful, since it should be reversible
without an intrinsic power source … which Mills’ theory describes. 

 

Three cheers for the redundant ground state part of the theory - which he
got right! 

 

So yes, Mills theory can explain the major part of the Parkhomov experiment,
but not all of it. And no, this device is not protected by any BLP patent
which I have seen. The theory of operation is not patentable in itself, only
a device - so even though Mills could (and possibly should) win a “big
prize” one day  - for the basic theory - he may miss the economic bounty of
a working device.

 

Unless that wildly sparking seam-welder does work for more than a few hours
at a time… J

 

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