Premise: If our ability to process incoming sensory information is the level of our consciousness, then an increase in this ability would create an increase in consciousness.

Overview:

At the time of this writing, there appears to be a form of matter, seen in the transition elements of the platinum group, that is nearly identical to material represented in various ancient religious texts as Manna.

This transition elemental material is found in varying amounts in air, water and rock but unseen by detection instruments due to a characteristic lack of valence electrons and, perhaps, may in fact be due to the transformation of all the electrons into bosons after a quantum energy state change.

This lack of electrons in the samples is indicative of a Bose-Einstein condensation of electrons as Cooper pairs, to form bosons. This forces the atom to have an internal temperature close to absolute zero at room temperature as the parts of the atom become stationary and no longer contribute to specific heat. In this condition the material acts as a superconductor in the Human body and that, in particular, Rhodium and Iridium are found in brain tissue.

Specific elements of the t-series elements have different effects on the human organism but all elements in this form can be extracted by a wet chemical process to be prepared as a concentrated nutrient for the nervous system to activate genetic processes.

Abstract:

Non-metallic transition elements that are present in ocean water, as the product of undersea vents volcanism and erosion deposition, can be extracted in a chemical process where pH is adjusted to cause precipitation of these elements out of solution.

Definition:

We will refer to these non-metallic transition elements as being in the m-state. These m-state elements are suspected to be in a monatomic or diatomic state with Cooper-paired/condensed elections. We also suspect that these elements are capable of becoming Bose-Einstein condensates themselves. We postulate that after positive screening field expansion and the associated forced pairing of valence electrons, the spinning deformed nuclei are in a condition that exhibits behaviors of a condensed ideal gas as a resonance connected quantum system of oscillators. M-state is our general term for these special-case atomic materials and structures. We use it generically in referring to all of the individual elements in this state though differences exist between them. The term "m-state" was chosen because it could refer to "monatomic" which some researchers still believe is the state of all of these elements. It could also be an acronym for microcluster state, mega-nuclear state, micro-atomic state or any number of other "m" properties that these materials are presumed to possess.

Logic:

Theories regarding the hydration and capture of the non-metallic transition elements found in sea salts are based on the observed addition of minerals into the oceans by under-sea vents (commonly known as smokers) and erosion from land by fresh water which is carried into the oceans.  It has been shown that sodic plagioclase and calcidic plagioclase ores contain 2400 oz. per ton of transition elements in modified 300 second spectroscopy in argon.

These elements are believed to hydrate into seawater and can be found in crystallized salt from evaporated salt sea water (see appendix C). Because these m-state elements have lost their ability to form metal-metal bonds, we believe that they can be regarded as Bose-Einstein condensates with an essentially positive charge (see appendix A).

We postulate that these elements replace sodium in the ionic matrix of crystalline salt.

• Physically: Metal atoms decrease in radius by more than one half after loosing the valence electrons to become positive ions.
• Electro-chemically: The atom is a positive ion as is the sodium ion.

In the case of gold, it is not uncommon to find monatomic and diatomic gold chlorides from AuCl₃ to Au₂Cl₆ and HAuCl_4. It is also common to find sodium aurides of up to Na₃Au⁺³. This indicates that gold can replace sodium ions in NaCl salt. Gold chlorides are a first step towards moving gold to a positively charged ion. In this process gold becomes stripped of valence electrons by the chlorine atoms after chemical bonds between them are broken by reductive elimination. After this gold can then form covalent bonds with sodium atoms as they give electrons to the now positive metal ion to fill in the missing three electron holes.

This process serves to initially provide aurous (Au⁺¹) and auride (Au^-1) that form gold diatoms which connect between 's' and 'd' shell electrons. These bonds can be disturbed by the addition of sodium with its 's' shell valence electron which defeats the aurous (Au⁺¹) 's' and 'd' shell electron bond between the gold diatom to form sodium auride, NaAu. This 's' and 'd' shell bond in metals is fairly profound--requiring a -2.50 V potential to overcome. However, 18 water molecules in a linear cluster hold a cumulative potential of -2.50 V and would allow sodium auride or disodium auride, in an aqueous solution of neutral pH, to form sodium hydroxide and a monomeric water-soluble auride. This auride would be made stable in its 'd' and 's' orbitals by a partial filling of those orbitals by water molecules. This function of water molecules would enable two opposite spin electrons from these different electron orbitals to form an ordered pair which would seemingly defy the laws of quantum mechanics regarding discrete shell locations for electrons of specific energy states.

The important difference in the two polyatomic forms, AuCl_(x) and Na_(x)Au, being that the gold atom stripped of valence electrons as an ion, Au⁺³, would have an affinity to ionically bond with the negative chlorine ions to form salt crystals, and form ionic bonds with negative ions in general to form precipitates. It would also show an affinity to chemically bond with sodium atoms to form monatomic and diatomic aurides, but almost certainly would not chemically or ionically bond with sodium ions which are positive.

We also suspect that an electrostatic bond might develop between the BEC gold diatom and sodium ions based on a theory employing the coulomb forces. This is still under investigation.

Some might speculate that the diatomic form of BEC gold, with twice as much nuclear material, would also have twice the electron valence charge--going from a relative charge of +3 to+6--but this view would be shortsighted as electro-negative charges are determined by valence electrons and the m-state elements appear to have no uncondensed electrons to provide these valence values, only positive forces by the preponderance of protons. Similar effects have been noted in supercooled helium 4 (see appendix A)

This would direct an opinion that the gold becomes a special case positive charge atom with a relative size and attraction slightly greater than or equal to the ionic attraction of Na+ as a replacement in the salt lattice.
 
 
 

Description of atoms and molecules of the Wet Method reaction

This reaction takes place in water. Water has been referred to in the ancient alchemy as the universal menstrum and does indeed have unusual qualities. Molecular clusters of water can act to remove electrons. Water has a natural tendency to ionize. The Ionization of water is shown in two commonly used equations:

The pH of a solution is the measure of the ratio of H+ and OH- ions as expressed in H+ ions as pH = -log [H⁺]. The natural tendency for water to ionize gives it an electrical potential which is essential in the ionization and neutralization steps of this process.

Oxygen is a non-metal with six valence electrons exhibiting a strong electron affinity. Oxygen increases in size once the two electrons are added during bonding. This completes an octet of outer shell electrons and a completed orbital.

Hydrogen is a metal with one valence electron. Hydrogen will decrease in size after giving up its electron bonding. It retains this smaller size as a hydrogen ion H+

Water is a dipole molecule. This means that when the hydrogen atoms each give up an electron to the oxygen atom, it causes the molecule to have a slight positive charge on the side with the two hydrogen atoms and slight negative charge on the side opposite these hydrogen bonds.

Hydroxide ion is a poly-atomic ion with a -1 bonding potential. It is also a strong electrolyte.

Sodium is a metal with one valence electron. Un-bonded sodium has a radius of .186 nm. When it bonds, it looses an electron to the atom it bonds with and its radius decreases, as a result, to .095 nm. When this sodium atom is separated from its bond, it is a positive sodium ion with a relative positive charge due to the loss of the electron but no change in the number of protons.

Chlorine is a non-metal and, like sodium, changes size by bonding. It has 7 outer shell electrons and exhibits a strong electron affinity. The relative electro-negativity is +3 and the atom increases in size in ionic bonding by the addition of an electron.

HCl is a strong acid and a polar covalent molecule. The chlorine atom has a great electron affinity with its almost complete outer shell of 7 electrons and it shares an electron with the hydrogen atom.

NaOH is a strong base and electrolyte. It will change the ion product constant for water as the sodium is hydrated away and the hydroxide is added to the existing hydroxides changing the balance of positive and negative ions.

M-state Gold is a metal that has lost its ability to electron bond due to condensation of all electrons and is technically a non-metallic form of gold. The attraction charge might me similar to a comparative valence potential of +3 to perhaps +6 as it is thought to have merged nuclei with a strong positive attraction force due to the condensation of its electrons. The atom, as a metal, has a period six atomic radius of .262 and it is suspected that the condensed positive ion or m-state atomic radius is near that of sodium. This might allow it to replace sodium in crystalline salt.

WET METHOD PRECIPITATION PROCESS

This method has specific steps to extract, concentrate and purify the materials for ingestion. The steps are as follows:
 

1. Initial precipitation at pH10.78
2. Separation of the precipitate from the reaction water
3. Washing the precipitate 3 to 5 times in distilled water
4. Re hydration of the precipitate at pH1-2
5. filtering the precipitate to remove solid contaminants
6. Re precipitation at pH8.8
7. separation of the precipitate from the reaction water
8. washing the precipitate in distilled water for ingestion
9. Collection and storage

Chemical reactant solutions:

• diluted HCl: Mix ½ cup muratic acid (20% HCl solution) in a ½ quart of distilled water
• diluted NaOH: Mix ½ cup 'red devil' lye (powdered NaOH) in a ½ quart of distilled water

1.    Initial precipitation at pH 10.78

Salt is dissolved in water. If sea water is employed the salt is already dissolved. If crystalline salt is employed, water molecules hydrate the atoms of the ion structure away from the crystal by overcoming the ion bond with the dipole water molecule. Typically it takes four water molecules to defeat the NaCl ion bonds to hydrate sodium and five water molecules to hydrate chlorine with the orientation of the water molecule dependent on the charge of the ion.

According to our theory, the m-state transition elements, with an even number of protons, and the m-state transition elements with an odd number of protons (forming diatomic double nuclei) have no free, uncondensed electrons. This would make them a special-case positive charged atom.

From this theoretical viewpoint, M-state elements would replace the positive sodium ion in the ionic matrix of the salt crystal. It is possible, however, that the odd numbered proton transition elements might condense with the unpaired electron being used in some modified valence bonding. This is under investigation

As the crystal is dissolved in water, the non-metallic transition element is hydrated into solution as illustrated below in the case of m-state gold. Again, these molecules form weak inter molecular bonds which serve to trap the m-state element inside an octahedral alignment of water molecules. This configuration of six water molecules is suspected to encompass the spin plane at the +x, -x axis and the +y and -y axis and the +z and -z spin axis .

2.    pH is adjusted to pH 10.78 using NaOH and solution is brought to a boil to sterilize the water and to bring out the maximum yield of precipitate.

As sodium hydroxide is dissolved in water, the sodium is hydrated and the hydroxide is released into solution. Hydroxide ions are not hydrated. As these hydroxide ions increase in amount they change the electro-chemical nature of the fluid. We postulate that they also replace the water molecules which have weak bonds with theBEC transition atom. As the strong OH- ion replaces the H₂O, in its bond with the m-state element the "molecule" is no longer held in solution and it falls as a precipitate to the bottom of the container. This would be a portion of the white slurry which has been observed.

3.    Separation of the precipitate from the reaction water

The removal of the top water (supernatant liquid), at this time, eliminates hydrated chlorine, sodium, excess hydroxide and other impurities still held in solution.

4.    Washing the initial precipitate

After the top water is removed it is important to also remove other materials of the reaction and washing the precipitate 3 to 5 times will remove unwanted chemicals still left in the separated precipitate.
 

5.    Re hydration of the precipitate at pH4

Diluted hydrochloric acid is added to bring the pH to pH3 or pH4 to re dissolve the precipitate. This step is to ensure that the sodium and magnesium hydroxide compounds are re hydrated and should be completely clear except for some solid impurities from the ocean salt.

6.    Filtering to remove solid contaminants

The clear solution is filtered to remove any solid contaminants from the seawater like clay, rock, shell, or metals.

7.    Re precipitation at pH8.8

Sodium Hydroxide is again added to this clear solution until pH8.8 is reached. This will yield a smaller amount of precipitate and this is because the magnesium has not precipitated and will not precipitate if the pH is kept below pH9.

8.    Separation of the precipitate from the reaction water

The clear top water is removed after the precipitate collects in the bottom of the preparation container.

9.    Washing the precipitate for ingestion

Distilled water equal to the amount of precipitate is added and mixed well. The precipitate is allowed to settle out again and the top water is again removed to further reduce any hydrated chlorine, hydrated sodium, hydrated magnesium and hydroxides from the reaction.

10.    This washing process is repeated three times. This further dilutes any undesirable components and moves the pH toward neutral. Some recommend boiling after the last wash to kill any bacteria which might have grown in the medium over the washing period. This is best done over a flame since some researchers claim that the m-state elements are driven off by fluctuating magnetic fields like those associated with electric heat sources.

11.    The material at this step can be ingested at a dosage of two tablespoons, one twice a day.

Before ingestion, the last wash should be boiled if boiling has not taken place before this step.

12.    Collection and storage

After the precipitate has been created it should be stored in glass or stainless steel, nested in a larger stainless steel container. It is recommended that a large amount of precipitate not be created as it is suspected that the material has a short 'shelf life'. This is indicated in the biblical references of the Manna found in the Sinai peninsula during the exodus as collected daily because it spoiled after more than two days. This may have been because of the lack of a sterile preparation environment but that theory is not defined in the texts. (See appendix E)

Testing the material

1.    The material resulting from the process described above through step 3 and the wash steps is believed to contain the m-state transition elements as well as calcium and/or magnesium. After the re hydration and re precipitation steps these materials have been removed. If either end step of washed precipitate is thoroughly dried out by baking it at a temperature less than 350 degrees Celsius the m-state iridium, platinum and gold solids will no longer be soluble in concentrated HCl.

2.    These elements can be further fractionated by heating them to 450 degrees Celsius at which point the m-state gold sublimates off. This m-gold will condense if bubbled through water or on cool surfaces near the flow of exhaust gasses. This will leave primarily m-state iridium and platinum.

3.    The other m-state elements which were dissolved can be re-precipitated by bringing the pH back up to 10.78. If they are dried again, the m-rhodium will sublimate between 900 and 1066 degrees Celsius and it can be condensed in the same manner as the m-state gold. Since the major portion of the m-state elements in sea water consists of rhodium, gold and iridium these parting methods should produce fairly pure fractions of these elements.
 

Reaction in digestion

We suspect that when the m-gold hexahydroxide enters the stomach, the hydroxides are once again separated from the transition BEC in the acid pH range of the stomach and, as in any acid with base reaction, are converted to water ( OH- + H+ to yield H₂O ) and salt. The transition BEC salt is hydrated (m-Au+ + 6Cl-) and we believe that it is absorbed into the system. This presumed reaction might be written:

6 HCL (aq) + M-Au(OH)₆   ---------------> 6H₂O + M-AuCl₆ (aq)

or as a total ionic equation:

6 ( H⁺ + Cl^- ) + ( M-Au⁺ + 6 OH^- ) -----------------> ( M-Au⁺ + 6 Cl^- ) + 6 H₂O
 

Evidence of this theory is seen during the initial precipitation step.

During the first precipitation, it has been noted that during the pH adjustment there appears to be a plateau where additions of NaOH is fluctuating in pH level and even going toward acid after an addition of NaOH. Then, suddenly, even a small amount of NaOH will dramatically raise the pH toward base.

This plateau is suspected to be the replacement of water molecules by hydroxide around the transition element as a 6 to 1 ratio of hydroxide molecules to transition element. During this replacement phase, the pH will fluctuate or not be changing at all due to this characteristic in reaction.

Toxicity:

Tests of the m-state transition elements on cell cultures (see appendix D) would seem to indicate that these elemental and micro-cluster elements are not toxic. There is a substantial body of anecdotal evidence that the m-state elements have a beneficial effect on human health. There is also some evidence that they were employed for this purpose in ancient times (see appendix E).
 

Precaution:

This ingestion, of a material that is very base, may require a small addition of acidic foods to help the body stay in a normal pH range.