Poser: does the bare proton: H- (hydrogen cation) aka "nascent hydrogen"
possess anomalous chemical energy, and is that energy related to why is it
neutralized so quickly?

With the Rossi report coming up soon (we hope) and the likelihood that it
will show "apparent" gain above chemical, but without gamma radiation or
other indicia of a nuclear reaction, we need to more closely examine the
magnitude of the "real" chemical energy available from hydrogen
manipulation.  It is not as clear-cut as you think, at least not when using
water as the physical model for hydrogen redox reactions.

The following presents the case for an apparent and "natural" COP of around
2.4 (6.8 eV instead of 2.85) being consistent with the real upper limit of
the chemical energy of nascent hydrogen neutralization via Ps. This is NOT a
related explanation to the one Mills gives in his theory, but it may sound
similar, since anything to do hydrogen (or positronium) involves Rydberg
multiples. It is not a violation of conservation of energy, if one admits to
the reality of the Dirac "sea".

In the case of positronium, the binding energy is 6.8 eV. Mills' theory
neglects the important role of positronium - and his view is tied to
redundant hydrogen orbitals. However, the best explanation for the rapid
(picosecond) neutralization of a free proton in nature is the ubiquity of
the Dirac "sea" of (virtual) positronium. Here is another version of Dirac's
field - epola, ps-BEC, ZPF or a host of other names for those who are
intimidated by Hotson.
http://www.epola.co.uk/introduction/precis/precis.htm

Perhaps Rossi will demonstrate a robust version of this curiosity, one that
has lurked in redox chemistry for decades going back to Langmuir's torch:
which is the possibility that asymmetric gain will be available in special
circumstances from sequential free proton formation and recombination. This
gain is actually quite similar to chemical energy but higher and
non-nuclear. 

In other words - there is a good argument that the "real" chemical energy of
hydrogen manipulation can be about 2.4 times higher than it seems from
combustion, due to an active vacuum and nascent hydrogen neutralization via
disruption of the binding energy of Ps (which energy remains in 3-space as a
UV photon). 

This argument will be continued in another post with more detail.

Jones

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