I think Mills was accurate about self catalyzing of fractional hydrogen
when trapped in a lattice, like cheerleaders forming a pyramid with the
lattice as just the ground floor I suspect they can dilate out from the
3d base structure of the metal lattice and form blankets of fractional
hydrogen in either temporal direction from the lattice.
The restriction for Mills/hydrino like condensation is given by the
symmetry of the fields and space. Orbits with same mass and topology can
condensate what means start a common rotation what classically frees
space-time what is equivalent to releasing energy.
As said: In the Holmlid case we see such orbit pairing going downhill
from 8 H* --> 2 4-He (8-Be) with a proton finally taking over the excess
energy. This has nothing in common with Mills model as there always must
be a final state with a higher stability/density = number of flux rotations.
There is just one more rotation possible for one symmetric mass pair and
thus there is only one H*-H* state fora a pair of protons where as D*-D*
can have 4 bonds.
Consequently the next H*-H* condensation only works if you have 2 H*-H*
and does not work not for a single pair. This is what Mills missed.
J.W.
Am 07.02.20 um 16:54 schrieb [email protected]:
Fran—
You seem to imply that nature changes depending on your observation
position—at the center of a local hydrogen at 3^rd base of a lattice
nuclet or far away in the batter’s box. Is my inference correct?
Also you suggest more than one temporal (time) direction. This
suggests 3 or maybe 6 possible time directions relative to 3^rd
base—up, down, back front left or right. Can you explain temporal
direction in more detail? Is there _no_ global time that applies to
all points in space, once that point is created?
Bob Cook
*From: *Roarty, Francis X <mailto:[email protected]>
*Sent: *Thursday, February 6, 2020 10:37 PM
*To: *[email protected] <mailto:[email protected]>
*Subject: *RE: EXTERNAL: Re: [Vo]:Superconducting Metal Hydride
Hi Jones, I still suspect Casimir geometry is actually relativistic
and the math they are using is giving the dimensions from local
hydrogen perspective while from our perspective the hydrogen inside
the hydride dilates becoming both faster and “relatively” smaller,
packing out further and further on the temporal axis while
simultaneously getting harder and harder to detect from the macro
world. I think Mills was accurate about self catalyzing of fractional
hydrogen when trapped in a lattice, like cheerleaders forming a
pyramid with the lattice as just the ground floor I suspect they can
dilate out from the 3d base structure of the metal lattice and form
blankets of fractional hydrogen in either temporal direction from the
lattice.
Fran
*From:* Jones Beene <[email protected]>
*Sent:* Tuesday, February 04, 2020 9:19 AM
*To:* [email protected]
*Subject:* EXTERNAL: Re: [Vo]:Superconducting Metal Hydride
I was hoping that this new discovery would show much tighter hydrogen
spacing - in keeping with the various theories for dense hydrogen.
However, the spacing is far from pico and not extremely compact at
all, and therefore this may result may not be related to LENR.
Fortunately, there is a lot of work going on in superhydrides - and
this work aligns with the long-held suspicion that a transient form of
superconductivity at greater than room temperature - and the
occurrence of LENR are somehow related.
Here is a related paper on another superhydride with a massive 9:1
atomic ratio. Ratios of nine or ten to one are possible with high
pressure.
https://phys.org/news/2019-10-impossible-superconductor.html
It is only a matter of time until a breakthrough occurs in this field
and the extreme pressures now being used, become superfluous.
Terry Blanton wrote:
*/An international team of researchers has discovered the hydrogen
atoms in a metal hydride material are much more tightly spaced than
had been predicted for decades — a feature that could possibly
facilitate superconductivity at or near room temperature and pressure./*
https://scitechdaily.com/room-temperature-superconductor-breakthrough-at-oak-ridge-national-laboratory/
--
Jürg Wyttenbach
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8910 Affoltern a.A.
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