A new paper “Thermally Reversible Hydrino Catalyst system as a new Power Source” http://blacklightpower.com/papers/EngPower032610S.pdf reinforces
my conviction that Mills and Haisch – Moddel are both very close but by refusing to incorporate components of each other’s theory are both still wrong. Mills new paper focuses on the difference between energy released in the hydrino state and the much lower energy required to convert the hydrides formed in the catalyst back to their initial form allowing the catalyst to work properly once again. Dr Mills was the one that inspired me to consider ashless chemistry but I appear to have taken it a step further by borrowing components of the Haisch Moddel theory involving Casimir effect and taping energy from ZPE. I think Mills is actually focused on “dissolving” a destructive by product that is “shorting” out the Casimir effect by forming whiskers across the cavities – the same problem the government is currently funding to prevent stiction in their latest nano endeavors. The ashless chemistry Mills should be focused on is powered by quantum forces that are antithetical to his GUT. These quantum forces are changes in Casimir effect that occur most dynamically with abrupt changes in geometry at the smallest scales like the pores in a skeletal catalyst or the Haish Moddel prototype (essentially a synthetic super catalyst). It is the these sudden changes in catalytic action that try to reform orbitals to new fractional values that disassociates molecular hydrogen reversing it back to atomic hydrogen numerous times before the thermal runaway caused the hydride reactions Mills is focused on in his paper. Haisch and Moddel make the same mistake in reverse, refusing to acknowledge that Mills is correct about the need for a chemical reaction to rectify the energy from the quantum effect. They seem to allow that the hydrogen must be disassociated to enter the cavity but then unbelievably think the f/h will Release energy as it transitions to smaller fractional states on the way into the cavity but be replenished globally by ZPE on the way out. Maybe it is 25 years of Power R&D talking but you need a rectifier – a knot- a waveform will transition symmetrically into and out of the same conditions unless you MAKE the path asymmetrical. The h2 molecule does this naturally, We know you have to force it through a membrane or heat it to disassociate it to get it to load into a lattice or even penetrate significantly into the confines of a Casimir cavity. My thought is this molecular bond is our rectifier and it not only resists the initial change to a fractional orbit but if it forms a fractional molecule it will also resist change to a different fractional value inside the cavity. That is the asymmetrical path that Causes ashless chemistry –You still have gas law (think ac component riding atop Casimir bias) based on uncertainty principle driving those gas molecules around inside the cavity and when opposed by abrupt change in Casimir effect will disassociate so the atoms can change to the new appropriate fraction for the new local geometry. Regards Fran
