Non Local Energy
Started by unknown · · 5 posts · last reply 16 July 2015
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#1 · date not recorded
Thorium is an element which is mildly radioactive, in that it is a weak beta emitter. (A beta particle is a high energy electron.) A common source of this metal is in the form of Tungsten alloy welding electrodes, which are two percent Thorium. (Not available in all countries.)
As an experiment, I took one of these electrode wires (1/16") and rolled it slowly, to see if this would add to the energy of the emitted electrons. While looking at it closely, I could sometimes see a really thin, overly jagged tiny yellow spark shooting out a distance equal to around three times the diameter of the rod. But sometimes a small yellow spot would light up briefly, then go out. These spots were much larger than the thickness of the little sparks, but there was no visible activity between the rod and the spot, which appeared about as far from the electrode as the length of the alternately appearing sparks. Therefor, I concluded that the spots were an example of non local energy. This is a type of energy associated with, but distant from, an electrode, capacitor, ion, or nuclear particle, without a conductive path.
The majority of published research into this energy is related to the field of nuclear physics. However, I've previously placed a relatively high amount of isolated charge on some paper, using an exotic HV potential. With more experiments, I fully expect to find out how to place non local energy within a volume of water. As mentioned, doing so will not require a conductive path. But the addition of this energy to the water molecules will cause them to expand and become unstable, at some point. Then, a vibrating HV potential applied to the water will simply shake the molecules apart. "Instantly".
It's pretty obvious that Stanley Meyer left something out of his patent, "for secrecy". He says the water molecules act as "micro capacitors", yet no mechanism is shown for charging them. Perhaps this is an angle which should be investigated. -
#2 ·
good point!
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#3 ·
I like your idea... i never saw something like that....
there were magnetic field in your experiment? wasn't a negative corona?
very interesting!
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#4 · date not recorded
"In chemistry, delocalized electrons are electrons in a molecule, ion or solid metal that are not associated with a single atom or covalent bond.[1] The term is general and can have slightly different meanings in different fields. In organic chemistry, this refers to resonance in conjugated systems and aromatic compounds. In solid-state physics, this refers to free electrons that facilitate electrical conduction. In quantum chemistry, this refers to molecular orbitals that extend over several adjacent atoms."
https://en.wikipedia.org/wiki/Delocalized_electron
"Delocalized electrons also exist in the structure of solid metals. Metallic structure consists of aligned positive ions (cations) in a "sea" of delocalized electrons. This means that the electrons are free to move throughout the structure, and gives rise to properties such as conductivity.
"Standard ab initio quantum chemistry methods lead to delocalized orbitals that, in general, extend over an entire molecule and have the symmetry of the molecule."
I've found that the right kind of energy can delocalize electrons, even in a piece of paper. Perhaps in water as well. -
#5 · date not recorded
It's known that the decay of a metastable state is exothermic. Being excited - of an energy above the ground state - it will eventually decay to a more stable state, releasing energy.
A search turned up the following quotes from this link:
http://chemistry.stackexchange.com/q...ring-stability
"Delocalization of π electrons makes a compound stable as the process of delocalization involves loss in internal energy. This is the synopsis of resonance.
"While studying resonance, I observed that one structure possesses charge while in other no charge. But in the final structure, there is, according to the book, partial charge present.
"So even with just 1 electron in a molecular orbital, where electron repulsion doesn't come into play, the longer we make the box (e.g. the longer the delocalization path) the more stable (lower in energy) the electron.
"the oxygen p orbital lone pair at right angles to the ring can overlap with the delocalised p orbital above and below the ring enabling a degree of delocalisation into the ring system so leaving a slight + charge on the oxygen. This in turn will reduce the electron density in the OH bond so weakening it"
So it seems that resonance itself is exothermic.
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