December 27, 2013

Depth: Ice II

   OK - we now have the set-up.  Millions of tiny water molecules are adhered to each other in a lattice of water that bridges together only water and excludes all else.  Since we do not have a hydrophilic surface to start the cluster - for the moment we will think of the pool of molecules as a massive cloud bank.  The atmosphere contains four parts nitrogen and one part oxygen and another few orders of magnitude less of everything else, water excluded.  The water in the atmosphere comes from evaporation of the waters on earth = heart = Gaia.  We've looked at clouds from both sides now with Carole King in the 60's - let's submerge ourselves into this collections of atoms at the size of the atoms themselves.

   Water is very small - in fact the nitrogen molecule is slightly bigger.  Atomic nitrogen and oxygen are dimers - two atom molecules that really have no affinity for the water and are glad to be excluded from the burgeoning water clusters.  Water seeds the clouds from many sources - the ocean and the jet stream are both major sources of this molecular mixing pot.  Individual water molecules have memory and can remember their previous environments, based on the information expressed in the form of the HOH bond angle and the lengths of the two oxygen-hydrogen bonds. We can read these energies using spectroscopy - the infrared spectrum of various waters has broad OH regions.  Doc has a collection of a dozen waters in the lab near Redding - waiting for the analysis capability to catch up to the mental gymnastics.

   When doc was working with Ormus, he came up with the idea that water attached to the atom of orbitally rearranged mono-atomic gold would adhere to the hydrogen atoms of water molecules rather than the normal oxygen side of the atom  This phenomena was uniquely different from the form of structured water that Pollack and Ho each formulated - the reasoning at a molecular level has to do with unfilled electron orbitals to provide a fairly substantial electronic affect - the Ormus gold acts like a pseudo-halogen with an unpaired electron buried in a stable form.  If you want more depth on this point - contact me separately.

  Gold atoms are 10 times the size of water molecule - a whole order of magnitude.  Thus enough water is directly in contact that the gold can serve as the point of nucleation for a water cluster.  The water would have inverted geometry to the oxygen based binding phase - the molecular spectroscopy of Ormus water will make a fascinating diversion once the lab is in place.  Water attached to the central gold is fixed as waters of hydration and each circular level away from the central sphere adds 1.6x individual atoms from the previous sphere.  There is less adhesion further away from the central gold - this would be a function of temperature as at higher degrees the molecular motion vibrations would take the individual atom and wiggle it out of the cluster.  This happens all the time as a function of the distance away from the center and the absolute temperature.  Our measures of influence change as a function of geometry - bonding can be directly measured in terms of bond lengths and the angle measured via optical rotation (by circular dichroism).

    Now let's theorize that somebody suddenly sprays a mixture of aluminum, barium and strontium ions into the atmosphere, perhaps that Mr. Keith person who was trying to sell spraying sulfuric acid into the air on the Colbert Report recently.  { https://www.youtube.com/watch?v=iku3lhAHJyQ } 

   The data from the snow melt on Mt. Shasta clearly demonstrate these three cationic components.  Each element here would strongly attract the oxygen atoms of water molecule - the very same oxygen atoms that are pointing outward and available in the lattice of Ormus gold.  If well distributed mixing occurs - then the cations might each be able to hold a unique hydration sphere around themselves, while still traveling within the boundaries of the morphogenic gold field.  The cations would repel each other and migrate to distances where they each have their field of influence on water - but do not affect the water of the next door neighbors cationic ion.  They also are not anywhere near the gold atom in space - the stronger affinity for water forms a tight exclusion zone that places the ion field around the central pseudo-halide.   This would have the effect of creating pocket of structure that interlace with other pockets of structure in a regular formation governed by the electrostatics and electrodynamics of the system.  In other words - the cation concentration!

    Thin about it - if a negative charged uberstructure attracts positive charged clusters, then the cationic morphogenic field would then super-collect anionic structures - or attract the negative oxygen end of nearby water molecules.  All this formal alignment would lower the entropy and raise the enthalpy and increase the temperature at which the structure could remain rigid, without cleaving off the individual water clusters as raindrops.  Instead, the package holds together until the weight of the ice formed is greater than the forces of gravity. Then - wham, pow - a high temperature ice storm reigns down upon the unsuspecting bovines.  Guess we would generate Mad Cows - another different aluminum topic with a magnesium kicker.

   So that's the theory that i would put forth for a viable means of nucleating ice to the point where it comes well beyond the temperature where it should have been converted to water.  I believe the science is good and the practice can be seen by those who are not in denial over the geo-engineering in the first place.  I would be more than happy to allow Mr. Colbert to grill me in front of a live studio audience, but alas - i have no book to sell or agenda to push.  Or perhaps, i do...

Namaste' ...  doc

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