pleiadian technology | book 1
- Metol
- Biosuperconductivity
- Metol Cholesterol
- Metol Fullerene
- Metol Growth
- Summary of Growth Processes
- Physics of Metols
1. METOL
The following is a description of the materials that comprise the hull structure of the flying saucer spacecraft. These materials are unlike any that are known to modern science, as they are what might be called “living metals,” that is, metals that have been grown into forms that are similar to those that are found in biological molecules.
These new materials are right out of a science fiction book. They are what you might call living crystal, based upon atoms that are above Carbon in the Periodic Chart. Tin and Lead are most commonly used, but so are Silicon and Germanium. In processes that were possibly known by the ancient alchemists, these materials are grown into molecules that mimic the behavior of biological molecules. They grow into long strings consisting of hexagons and pentagons like organic proteins and fats, etc.
The magnetic atoms can be iron or nickel or other magnetic atoms, while the diamagnetic ones are copper, silver, and gold. The diamagnetic atoms play an important role in the functioning of the unit cells of the metols, but they do not form strong bonds, either with each other or with other atoms, and so their number must be limited within the unit cell crystal structure, or else its structural strength will suffer.
The bulk of the magnetic atoms do not occur in the side chains. The ones that are implanted into the hexagonal sheets only act as nucleation sites for the much larger group that are in the core of the crystal. Each single crystal has a core of these heavy atoms. This core acts as a nucleation site for the growth of the framework atoms into the sheets. During the crystal growth phase, the core magnetic atoms are attracted to, and migrate toward, the magnetic atoms in the sheets. This process is similar to the one that occurs in doped glasses that change from completely transparent to slightly occluded when they are exposed to either infrared light (heat) or ultraviolet light. The nature of the metol is altered considerably when these magnetic and rare earths atoms form small latticework inside the larger framework of the sheets.
The rare earth elements enhance the magnetic fields of the magnetic atoms, and also provide positive nucleation sites for the growth of the superconducting sheets that are a separate material from the metols, but are attached to them. These atoms serve as “enhancers” for the three desired effects that occur when these crystals are excited by electromagnetic fields of the appropriate strength and intensity.
One of the special effects is that of “superluminosity,” where the dopant atoms are induced into phosphorescent states that are considerably greater than those that can be achieved in exiting crystals. Another effect is that of “supermagnetism,” where the rare earth dopants enhance magnetic field strengths to very high levels. This is already being done in the existing material sciences. The last effect is that of superconductivity, which also is being achieved by the existing technologies. All of these effects, and particularly that of superluminosity, are greatly enhanced over what is currently known.
The last remaining structure of the crystal is its exterior sheath. This gives the crystal its personality, and makes every crystal different. In the earth, the outer layer is the crust. In a living cell, it is the cell membrane. In the metol crystals, it is a layer of superconducting atoms.
In the metols, the surface atoms occur in an entirely different structure than they do in the interior sheets. This new structure occurs in the known SC [superconductor], such as the Perovskite family of crystals. It is that of the “square plane matrix.” In the membrane of living cells, the phosphorous atom forms a square plane pyramid with four oxygen atoms. This structure serves as a positively charged nucleation site for the growth of a SC square plane on the exterior of the cell’s membrane. The SC square planes consist of four oxygen atoms that form a square around a single diamagnetic atom.
In living cells that are based upon hydrocarbon chains, the diamagnetic atoms are either phosphorous and sulfur, or copper and zinc. Most of the superconducting reactions that occur in the human body are based upon the heavy atomic group of copper and zinc. When electrons superconduct over the surfaces of cell membranes and other membrane structures, the salt compounds of these atoms form superconducting squares as they bond to the phospholipid membranes that have a cubic lattice structure. Intracellular and intercellular communication takes place through these planes, as messages are transmitted on the superconducting electrons.
The spacecraft metols have superconducting square planes on their surfaces. These planes are deposited there when the final unit cell metols are compacted together to form the single cell grains.
2. BIOSUPERCONDUCTIVITY
These crystals are superconductive at room temperatures. There is a reference work that proves superconductivity in cholanates, which are related to cholesterol, at room temperature. These new materials have the structure and operational properties of the organic cholesterol and protein molecules found in animal bodies. They will be able to tune into the information that is in the psychic fields, which are living fields of information and intelligence. They will make your dowsing work simple, as you will be able to physically “see” what you are able now to only sense.
Along with the form of biological molecules, such as proteins, these materials perform a task that is a unique function of some biomolecules, that of the conversion radiant energy (light) into a chemical bonding energy. In biomolecules, this conversion process produces the “bio-energy” that cells use when they synthesize a new molecule from one or two others. In plants, bio-energy is produced in photosynthesis, where carbon dioxide and water are converted into cellulose material, which is the basic building block for this form of life.
The bio-energy that animals use is produced during the ATP-ADP-AMP cycle. ATP stands for adenosine tri-phosphate, ADP for adenosine di-phosphate, and AMP for adenosine mono-phosphate. When the cells of animals consume they energy, it must be derived from the “ATP-ADP Cycle”, where ATP is converted into either ADP or AMP. Energy that the cell can use is liberated during this chemical conversion.
The cells of animals use this form of energy to perform all of their biological functions. The building of protein chains and structures, the synthesis of new cells, and all enzymatic processes use bio-energy from the conversion of ATP into ADP or AMP. Even muscular contractions and work require this form of energy.
Plant life converts the energy of sunlight into the force of a chemically induced contraction during photosynthesis. In animal life, food is consumed and then oxidized to provide energy that, in turn, is converted into the chemical bond energy (force) of the ATP molecule.
The spacecraft materials are “living” in the sense that they not only have the same structural shapes as living molecules, but are also able to convert their energy into the bio-energy of a force field. This force field, however, instead of being used to synthesize new molecules, is used as a “counter-force” to the force of the earth’s gravitational field as it acts on the mass of the craft. This force does not, strictly speaking, propel the craft through space, as it is not a propulsive force. It is a gravitational type force field that creates a localized center of gravity inside the craft. This center then pulls on the center of mass of the ship, (actually all of the mass of the ship), and the ship moves off in the direction of the vector that runs from the center of ship’s mass to the center of artificial gravity.
The craft’s materials have a geometrical conformation that mimics those of biomolecules. As with biomolecules, the spacecraft materials are molecular crystals, long chains of individual molecules that have been bonded together. In biomolecules, a good example of this is the formation of protein peptide chains from individual protein molecules which, in turn, are composed of amino acid sequences. (NOTE: there are only twenty different amino acids that make up all of the protein structures in the body).
One of the prerogatives of creative scientific writing is that the author is allowed to make up certain terms that might be more descriptive of what he or she is talking about. I have chosen the term “metol” to describe the remarkable materials that are used in the construction of these craft.
The term “metol” is a contraction for “metal cholesterol,” and has been chosen to describe these materials because their structure and operation mimics that of the cholesterol molecule in the bodies of animals. The structure of these materials is close to that of the collagen proteins that are the basic constituent of the muscle fiber of animals, and there is also a form that resembles the helix structure of DNA.
Nonetheless, because these materials function in the manner of cholesterol, and because they are composed of metal atoms instead of carbon, nitrogen, oxygen, and hydrogen, they have been given the generic name of “metols.” This term will be used a great deal in the following text, and it seems appropriate that they be given a title that is more familiar than “these materials.”
3. METOL CHOLESTEROL
The main body of the cholesterol molecule consists of a series of hexagons with branching side chains on one end. The hexagons have open sides that provide bonding spaces to other molecules, usually with the negatively charged ion of the water molecule, known as the hydroxyl ion. The side chains molecules of the cholesterol family of molecules are simple hydrocarbon sugars. These sugars usually have too few hydrogen atoms, and for this reason are also electrically negative in charge.
In human and animal bodies, one cholesterol molecule bonds to the next cholesterol molecule when its side chain attaches to a vacancy in the hexagonal chain structure of the second molecule. The side chains twist when they bond to the next complete molecule, and this gives the molecule complex a spiral structure. When light is shown through one of these molecules, it is rotated by the interaction of its electromagnetic fields with the spiral side chains of these molecules.
A single cholesterol molecule is as small as any other biomolecule, less than 20 Angstroms in size along its longest dimension, but because of the property of optical rotation, many hundreds of them can be twisted together into a single molecular complex that can be as large as 1000 Angstroms along its smallest dimension.
The craft’s metol has the property of “biological conformation” to its chained hexagonal structure. This property occurs only in “living” cells, i.e., those that are able to take part in the basic biochemical activities that build new cells from the raw protein materials that are taken into the body. If the successive structural members of a protein chain are crumpled or puckered instead of lying flat, they have the property of conformation and will act as if they are alive. Identical structures that are flat instead of crumpled in their structures will have the same chemistry but are not crumpled will not take part in the biochemical activities of the life process.
The property of conformation, as it occurs in puckered hexagonal structures, also occurs in hexagonally bonded groups of water molecules, and in most silica crystals as well, quartz crystal being an example of one of these.
Metols are similar in structure to the Bucky Fullerenes that have recently been grown by material scientists. However, unlike the Bucky Balls, these structures do not have the closed, spherical symmetry of the Fullerene crystals.
The craft’s metols are grown in a process that is similar to the one that is used to fabricate the Fullerenes. However, they are put through a “First Stage” crystal growth and the Fullerenes are not.
Metols are composed of atoms in three basic types of geometrical alignment: crystal core, framework, and spiral chain. The framework atoms have either a negative charge or a positive charge to their overall structures. The charge nature of these structures correspond to their curvature in space. A positively charged framework is similar to a Fullerene type of crystal. Its surface curves over on itself and completes itself in a collection of polygons (hexagons and pentagons) that can be inscribed into a sphere or ellipsoid.
The negative valence molecular radical has a natural tendency to fold outward as this radical seeks a positive radical with which to bond. The positive radical, on the other hand, has more of a tendency to fold inward and to maintain an integral and completed structure, such as that of a Fullerene Crystal.
A negatively charged framework has a negative or outward curvature to its surface that does not terminate or fold over on itself. These surfaces are two-dimensional sheets instead of three-dimensional spheres. A negative framework can take on any curved shape, as long as it is infinite, or potentially so.
Using the definition that has just been given, most biological molecules would qualify as having negative hexagonal and pentagonal surfaces and positive side chains which have a spiral geometry. Their surfaces are not only charged negatively, but they have the open conformation of the negative surface. In molecular groups, biomolecules form long chains, this because these surfaces will not fold over on themselves.
The cholesterol and phospholipid (fat) molecules, for instance, have hydrophilic chains that are water soluble and have a positive charge, and hydrophobic “frames” that have a negative charge and are not water soluble. The hydroxyl water ion (OH-1) has a negative charge, and that is the reason that it is able to bond with the positive side chains of these biomolecules. The other half of the water molecule is a hydrogen ion (H+), which does not usually form bonds with biomolecules, however, it does bond with water molecules.
The positive framework crystalline forms have been recently discovered in the Fullerene crystals that are composed of the element Carbon, and sometimes other atoms as well. The surface of these structures…describe here…[:sic]
The severe folding of the metol framework at the terminus of their spirals puts a great deal of pressure on the hexagonal latticework. The lattice structure is so compressed that an abnormally high degree of optical rotation and nonlinear frequency shifting is generated in the light that is put through these crystals when they are in their transparent phase. The frequency shifting occurs through a range that is the shift from the valence to the conduction band of the crystal’s framework atoms. The pressure of the lattice structure, plus the intensity of the local magnetic fields from the magnetic atoms in the side chains of the metols, converts the energy of the light into the weak nuclear force field that becomes the basis for the craft’s propulsion and lift against the force of gravity. This is identical to the conversion of light energy into a molecular bonding force through the process of photosynthesis??? [:sic] in certain plant molecules and structures.
The final form of the metol takes on the “organic” appearance of the onion, which has many hexagonal layers of carbohydrate molecules. The crystals, like the onion, have small depressions in the tops of their structures where there is a concentration of “seed structures”, and their bottom ends tail away so that they have an elongated shape. At the heart of the onion lie the seed crystals.
The size of the light cell crystals varies slightly, depending upon the many variables that can occur in the growth stages. The most probable range of sizes is from 100 to 300 Angstroms in length, and about one-half to three-quarters of that in diameter (they are rounded). Within each light cell there are many individual spiraling sheets of framework atoms. Between the framework atoms, in the side chain positions, lie the magnetic effect atoms, while the dopant atoms that are the basis of the phosphorescence occur regularly throughout the interior of the structure, yet are concentrated towards the crystal’s top end.
4. METOL FULLERENE
Negatively charge frameworks have an excess of electrons and a net negative charge. The presence of a negatively charged structure indicates that its density would be less than that of the same structure if it had a positive charge. This is because the former condition is caused by too many orbital electrons, which increase the negative charge on the structure and increase its size (diameter) as well. The positive surface condition is caused by too few electrons, which result in an overall positive bias to the charge, and a smaller diameter for the atoms that make up the structure. Currently, all of the Fullerenes that are grown have a slightly positive surface charge, because the radii of the carbon atoms is slightly less than the radius of the neutral carbon atom. This implies that there are too few electrons in the structure, and hence a net negative charge.
The transition from a positive to a negative framework occurs inside all of these crystals which are alive with vibrations, both phonon and photon. This transition is part of the growth process of these crystals. During this process, the positive framework is joined to the negative framework, and when electrons are added to the former, the force of their charge expands them into negative frameworks. As they are expanding, they push against one another until the framework buckles into the shape that is consistent with that of biological conformation. Only negative frameworks are alive with the structure of living biological molecules.
If the negative framework does not buckle under the electrostatic pressure, it will expand through cleavage. This is where the hexagonal and pentagonal framework actually breaks along a line and moves over itself. This movement is the beginning of a spiral that will eventually produce the second atomic geometry (geo-atomics) of the final crystal form of the metols.
The third geoatomic form is that of the matrix-centered dopant atom. This is identical to the arrangement of cation dopants and anions that are found in many types of crystals. Those are used in solid state lasers, such as the Nd-YAG (Neodymium-Yttrium-Aluminum Garnet) Laser. The sapphire crystals (Aluminum Garnet) that are used in these lasers have Yttrium and Neodymium cations doped into their lattice structures. The lattice structure is anionic (of net negative charge), and it exchanges its excess electrons with the cations in the electromagnetic process of spin resonance, during which a high frequency vibration occurs between the anion matrix and the cation dopant atoms.
In the metols that make up the spacecraft, the dopants are usually rare earths. In a manner that is identical to the growth of the lazing crystals, these dopants are added to the mixture of framework atoms, and the unit cells form around them. These dopants add a high degree of luminescence to these crystals when they are irradiated with ultraviolet light and x-rays.
5. METOL GROWTH
The growth processes for the metols have been described briefly, but not with any detail. While there are three basic units to these crystals‒the quasi-crystal seeds, the hexagonal sheets, and the superconducting squares‒there are only two types of growth processes.
The First Stage process assembles atoms into the three basic structural units that were described above. The quasi-crystals, with dodecahedral and icosahedral symmetry are grown from the three predominant atoms in the crystal lattice. These are the framework atoms (usually the quadrivalents), the magnetic atoms, and the diamagnetic atoms. The framework atoms are grown into crumpled hexagonal sheets, which have a two-dimensional symmetry. The superconducting sheets are composed of framework atoms with a negative (instead of a positive) valence and diamagnetic atoms. These, too, are grown into sheets, but with a different conformation, and with different growth procedures than the hexagonal sheets.
The superconducting “square plane” sheets and the hexagonal sheets are grown in an “alchemical” process that involves the use of acids (gases that have been dissolved in water). Specially designed chambers having many different types of silica crystals are used to create an environment where the property of conformation can be put into the sheets during their growth cycle. The final product of the First Stage Growth for the hexagonal sheets is a crystalline form that has many of the properties of crystallized silicon. Crystallized silicon, like that used in the semiconductor industry, grows in hexagonal sheets. It is a brittle metal with a conductivity that varies with the number and types of atomic dopants that are added to its structure.
In the Second Stage of crystal growth, the metol crystals are grown in an environment that is similar to the one that occurs in outer space when the high energy solar wind impacts the earth’s magnetosphere. The planet earth can be considered to be the seed for the growth of the larger crystalline structure. The “earth seed” has a core of magnetic, heavy metal, and rare earth atoms that have a strong magnetic field. Surrounding this core are layers of silica-based crystals with lighter metals, such as aluminum and magnesium, implanted in their structures.
If the earth were in a very hot, molten condition, and the solar wind was about a million times its current energy density, then the conditions would be correct for the growth of the metol crystals. The core atoms, which are all metallic, have previously been grown into a variety of shapes and sizes, the basic geodesic structures being that of the quasi-crystal. The quasi-crystalline core provides a single, large nucleation site for the growth of the mantle, which has a polycrystalline nature.
The mantle of the earth is comprised mostly of silicates in crystalline, polycrystalline, and amorphous crystalline forms. Silicate crystals grow into hexagonal layers which have a two-dimensional symmetry. On rare occasions, these layers form geodes of three-dimensional quartz crystals, which have additional tetrahedral bonds between the layers, but these crystals rarely form, and only when the growing conditions are correct.
The metol crystals grow in a manner that is similar to that of the growth of the “earth crystal.” The metal core atoms are grown initially into a group of quasi-crystal unit cells. These unit cells are placed under high pressure, and as a result, surface electrons are forced away from them, and the total mass of the composite material, consisting of many unit cells, develops a net positive charge.
The positive charge of the mass of core atoms acts as a nucleator for structures that have the opposite or negative charge. In the earth crystal, the negative materials are the silicates that form into the mantle, but in the metols, sheets of metals that have been converted into the crumpled hexagonal sheets of living crystals substitute for the silicates. These sheets are grown onto the surface of the quasi-crystalline core while they are in a molten condition.
At the zone of interface between the core and the mantle in the earth, (which corresponds to the interface between the seed metals and the metol sheets), many thousands of small spiral crystals develop. These spiraling crystals consist of several quasi-crystal seeds that act as nucleation sites for the metol sheets, which spiral down in vortexal patterns towards the seed crystals. The high levels of positive charge in the seeds is counterbalanced by an equally high level of negative charge in the sheets, and the sheets become very compacted in their hexagonal structures as their atomic diameters increase. This puts tremendous pressure on their developing lattice structures. As a result, these new crystal forms have very high indices of refraction and very pronounced nonlinear optical effects. When light is put through them, it is refracted through almost a ninety-degree angle, and when this light is further circularly polarized, it will circulate in a spiral pattern inside the crystal.
Spiral nucleator crystals are only grown between the core seeds and the hex sheets. In the growth process, these develop between the large mass of sheets and the core in growing chambers. Small pieces of both sheets and magnetic core atoms break off and form into the metol unit cells. The sheets are curved and compressed down to a conical shape that has core atoms at its terminus. The positive core atoms move out to meet this incoming spiral of sheet material (negatively charged) and a helix is the result.
These crystal forms are then collected and regrown together with additional sheet atoms into the final metol unit cells. The additional sheet atoms hold the smaller helix units together. In this process, an electric field is used to align all of the helices in approximately the same direction, usually that of the long axis of the “egg” shape of the crystal cell. When these cells are assembled into the micron sixes grains [ sic], which mimic the biological activity of a living cell, a magnetic field is used to align their axes perpendicular to the grain’s surface. This field is also used to create spin alignments between the individual constituents of the cell [see below].
This is similar to cholesterols in lipid membranes where the spiral sugars are perpendicular to the membrane layers. This configuration provides info that helps align the membrane sheets that are grown onto the surface of the grains.
The grains could be called “spin cells” because electromagnetic frequencies that induce ESR are used. ESR or EPR is a phenomenon where a magnetic field can be used to cause the electrons that are shared by an anionic and a cationic structure in a crystal to resonate together. Usually mag fields of 3000 – 5000 collages are used.
In these cells, ESR can be induced between the anionic sheets and the cationic materials, either magnetic, diamagnetic, or rare earth dopant. These frequencies are generated in a laser beam that is tunable to certain frequencies in the Rydberg series for the element hydrogen, or for other frequencies that are in the Schuster Series for the element sodium. As it turns out, the ESR frequencies are resonant to the size of the grains if they are generated as acoustic frequencies and propagated at the speed of sound. The done with A-O generators. The grains are also resonant to electromagnetic frequencies that are in the infrared range.
A combination of frequencies [ESR in the 1 – 10 GHz range, and IR in the 100 – 300 THz range], as well as the appropriate valence and conduction frequencies for hydrogen are all used in the growth process of the grains. The metol unit cells are assembled into grains which are then subjected to these combined fields, including the ESR resonant magnetic field.
This last field polarizes the metols so that their axes are perpendicular to the grain surfaces. This is accomplished by circular polarization of electromagnetic waves through the cell as the magnetic field develops unidirectionally and as the electric field circulates.
The anionic sheets are the most difficult to fabricate because, as mentioned, geodesic fullerenes naturally develop positive charges, behaving as if they were large cations, (the positive half of a molecule). All of the fullerenes that have been grown to date have small positive charges built into their structures. These charges are not a product of the normal quantum atomic orbitals that occur in most cations. They are, instead, specialized charge levels that have been grown into the sheets. As with any electric dipole field, these charge levels can take on any fractional value.
The infolding, positive curvature of the fullerene geodesic is a product of its net positive charge. Anionic surfaces, on the other hand, have negative curvatures that are out-folded. These surfaces do not make closed structures, such as the fullerenes. Instead they form into broad sheets that have the potential of never terminating. The out-spiraling of the anion polygons that occurs in the magnetic spiral cells breaks through the positive surface of this cell at the top of the cell. These spirals then connect into the superconducting sheets, which grow orthogonally to them.
In the cell structures that are under consideration here, the anionic material with the greatest negative charge level (in excess of 2.0e) is the superconducting sheet material that forms on the surfaces of the light cells.
The first anionic sheets that are grown will have only small negative charge levels, perhaps in the range of .1e – .2e. But as these sheets are grown and regrown in the crystal growth chambers, their valence (charge) slowly increases to the desired levels of the superconducting sheets. As this change is made, a corresponding change in lattice structure develops, as the hexagonal-pentagonal alignments are transformed into square plane alignments of the superconducting sheets.
The transformation in the charge that occurs in the materials is paralleled by a change in their form. The square plane sheet develops spontaneously during the magnetic-rotator growth cycle for the [sic: photoluminescent?] crystal cells. In this cycle, magnetic nucleation centers develop that change the symmetry of five hexagons surrounding one pentagon into four hexagons that are independently bonded to the magnetic atom. This requires the severe bending of the geodesic form in order to eject one of the hexagons.
The new form for the geodesic is based upon a collection of hexagons, pentagons, and squares. This structure conforms to that of the myoglobin molecules that make blood cells in the bodies of animals.
Part of the electronic operation of these cells is a product of the electronic forces that occur between the oppositely charged positive and negative surfaces. Constant changes in charge levels occur between these layers, and the forces from these changes keep the cells vibrating with sonic energy.
The center spiral axis of magnetic atoms in the magnetic cells is a quasicrystalline structure that has a symmetry that is based upon the number five. Quasicrystals have three atoms in their structure, with one principle atom dominating. Their stoichiometry is based upon 100 atoms, and for this crystal, the ratio of 50-30-20 prevails, with iron or nickel being the main atom.
The outside atoms in the central axis of the spiral cell are usually part of the hexagonal symmetry of the geodesic structure. They occupy the two inner positions in this structure. Usually, there are five hexagons that surround one pentagon in a geodesic, but for the negatively charged anion sheets, the pentagon that is at the center of the spiral is missing, and so the five hexagons are compressed slightly toward one another. This produces a rotation in the next layer of hexagons, as the structures begin the slide under one another. This symmetry is close to that of the angular layers of the quasicrystal, and this convergence at the center of the spiral cell produces a final spiral form that is a combination of both of these forms, the rhombohedral quasicrystal and the compressed, spiraling hexagons. Eventually, at the bottom or small end of the spiral, the five hexagonal symmetry has been replaced (or compressed) into a four hexagonal symmetry. This changes the angles of hexagons from 72 degrees to 90 degrees, and mimics the myoglobin molecule of blood cells.
This odd symmetry can only be maintained if the atoms in the center axis have the rhombohedron structure that has been proposed in the one mathematical theory that has explained the symmetry of the quasicrystal, that of non-consecutive tiling. In this symmetry, the atoms that compose a quasicrystal have their layered arrangements in rhombuses and their three-dimensional structure in rhombohedrons.
Successive layers in quasicrystals are offset to one another by a small angle, the vertical angle of the rhombohedron. If sections of the crystalline structure are rotated, then a spiral geometry develops about a center point. This symmetry produces vortexes of electrical energy inside the crystal. It is produced by the introduction of a dopant rare earth atom, which acts as a nucleating site for the growth of a spiral section. These sections fit together loosely and with many vacant spaces on their edges. These become areas for the discharge of photons of light.
The quasicrystal sections are based upon the circular areas in the Penrose Tiling Scheme. They occur in an irregular fashion throughout the crystal. These areas charge up positive and negative with the electrical current. When a positive and negative pair come together, they merge slightly, and the van der Waal forces are produced in the area. These are the lifting forces for the craft. They can be seen in the reference on protein structure (SCI. AM. April 1986).
Quasicrystals have pairs of atoms that produce small vortexal areas within each pentagon framework of the crystalline structure. These are based upon groups of magnetic-diamagnetic atoms, such as the silver-nickel atoms that occur in the craft material. These groups occur in the quasicrystalline lattice structure as cations. They can occur in groups of two, three, four, or five atoms that are in close proximity, this because of the small radii of cations when compared to anions.
The cation groups occur along with single anions. The total charge of the cations and anions usually never quite cancels. In the known quasicrystal, Mg32(Al-Zn)49, the cation pair of zinc and aluminum hold positive charges of “+3” and “+1” respectively. Zinc can also have a charge of “+2”. The anion is magnesium, which normally is a cation, but has been forced into an anionic configuration by the crystalline lattice, and so holds the large negative charge of “-6”. The total negative charge for the 32 atoms is “-192”, and the total positive charge for the 49 atoms is “+198”. This charge imbalance can be redressed by adding atoms with a net charge of “-8” to the structure.
Because they are of like charge, the magnetic-diamagnetic atoms in a quasicrystal repel one another. This force is countered by the lattice forces that hold the crystal together. These are related to the van der Waal forces, which develop when electromagnetic reactions occur entirely inside of a molecule. In this case, the negative electric field of the electron cloud interacts with a complex set of frequencies with the positive cation field, and the force field is produced. The frequency sets take the energy of single photons and convert them into a force field that acts through a distance, and this is the basis of the craft’s lift and propulsion.
Spin oscillations occur in these areas. This is a new area of quantum mechanics, as the spin is reversed in a continuous pattern with its rate. Sometimes the rates vary and the spins reinforce or annihilate, the former energizing the electrons in the atomic vortexes and the latter ejecting them into a superconducting state. This is the atomic vortex equivalent of the larger crystalline vortexes, which are grown and programmed into these crystals at all phases of their growth.
The spin rates are the heterodynes of the spin multiples that occur in the spectra of atoms. In this case, the magnetic-diamagnetic groups of atoms are continually oscillated between a zero-spin condition in the diamagnetics, and a plus and minus spin condition in the magnetics. The zero-spin rate is usually much lower than the plus or minus spin rates, but it also functions independently of the other two, which are dependent upon each other, as they are the reverse of one another. In terms of electronics, the zero-spin state is the “on-off” rate for an oscillating system.
The basic structure is the expanded geodesic framework of the cube. The individual geodesics are grown into a shrunken and positive condition. They are so compressed, and the framework atoms so close together, that free electrons on the surface, the ones that are SC, are able to temporarily occupy inner orbitals where they can emit visible light instead of producing the normal infrared radiation that is associated with the outer electron orbitals of atoms.
The expanded structure is thus composed of shrunken geodesics. After this structure has been grown, dopant atoms are injected into the spaces between the geodesics in the cubic lattice. These occupy edge-centered positions in the main cube and face centered positions in the body-centered cube. In the SC metol, these are diamagnetic atoms, and when they fill the spaces between geodesics, they create diamagnetic centers.
The diamagnetic atoms in the lattice structure are in a highly ionized condition, and so their radii are also much smaller than would occur in other lattice structures. Several of them can group together in one diamagnetic center. If there are missing geodesics in the lattice, referred to as “voids,” the geometry of the lattice changes at that point. The remaining geodesics pull in closer together, but there is still a large volume of space in the void. This space can be filled with even larger numbers of dopant atoms than the normally occurring spaces between the geodesics in the filled lattice. This creates larger diamagnetic (or magnetic) centers in the crystals’ lattice structure.
The expanded geodesic lattice structure is grown into layers that have a submicron thickness. This, too, is not random, but is related to, and governed by, the wavelengths of the light that is used as the basic “fuel” for the propulsion system. Successive layers of the metol are machined to act as wave guides for these photons, so they must have a certain thickness.
The SC lattice is the 4-symmetric portion of the 4-5-4 metol sandwich. It is the SC electrons that have zero spin. The other lattice section is the 5-symemtric quasicrystal. This is the optical portion. The electric fields inside this crystal are so intense that they are able to bend light through angles that are unheard of in the known classes of nonlinear optical crystals. These fields develop between localized areas that are alternately positive and negative in their charge.
The charge of the metallo-optical crystal is grown into the atoms in the crystal’s lattice, and is identical to the internal charges that exist in all types of optical and piezoelectric crystals. There are anions and cations in the crystal’s structure, and the electrical oscillations between them bend the light into a near circular form.
This crystal is quasicrystalline only in its symmetry, which is based upon the number five as it occurs in the geometrical figures of the pentagon and decagon. It does not resemble a quasicrystal as we currently understand them and as we have grown them in our material sciences labs. The anions of this crystal are actually the same positive geodesics that are used in the SC lattice. They are converted into anions when their positive charges attract negative electrons to their surfaces. The difference with these crystals is that, unlike the SC ones, they do not readily conduct electrons, so once the spaces in their lattice are filled with electrons, they become trapped there and are not able to leave the lattice.
The trapping of electrons is accomplished by doping magnetic atoms into the lattice instead of the diamagnetic atoms in the SC portion of the sandwich. These atoms occur in groups along with a few diamagnetic atoms, and the oscillations between them, which are controlled by their electron spin frequencies, trap electrons and spin them inside the lattice. This spinning motion produces very large magnetic fields that are localized in the 5-symemtric layer of the lattice. Ordinarily, these magnetic fields would destroy the SC qualities of the SC crystalline lattice, but they do not in this case because they have a very low level of coercive force, and when the current is turned off, it collapses quickly.
In its down or collapsed phase, electrons are ejected from the optical material onto the SC layers. They move through the lattice in this cycle of the operation of the electrical system. Initially, a high voltage current is sent through the SC to prime the optical crystal. This high tension field creates a maximum rotation in the light as it moves through the optical crystal. It is similar to exciting a fluorescent tube with a high voltage current before dropping down to a lower voltage and higher amperage current, which then is the “steady state” current.
As the voltage drops in the metol, the amperage increases. This decreases the optical rotation and bending of light through the crystal, but the magnetic trapping of electrons is increasing as the amperage of the current is increasing. This builds to a maximum until the current is suddenly turned off (the generator is in its down or relaxation phase) and the many small internal magnetic fields collapse and eject electrons for SC.
6. SUMMARY OF GROWTH PROCESSES
1. In step one, the framework atoms are grown into hex and pent sheets that have a negative charge to their structures. This charge put in by growth with inert gases, causes them to become ionized into positive ions in the growth process. These react with the framework atoms, much as they do with halogen gases in an excimer laser, and convert or program them into anions. Simultaneously, the sheets are grown in arcs similar to those that are used to grow the Bucky Balls. The sheets are crumpled into their biological conformation in step two below.
2. In step two, the “helix cells” are grown. A piece of machinery called a “crystal magnetic rotator” is used to grow the “helix molecules.” These are molecular crystals, that is, molecules which, like biological molecules, can be grown into larger molecular complexes. The growth of peptide chains from individual protein molecules, which in turn are amino acid sequences, is an example of molecular crystals.
The rotator “machine” is comprised of complex silica-based crystals, such as ruby-garnet, magnetic atoms, etc.
The rotating magnetic field interacts with the crystal and has its lines of force curved through almost a right angle. Small vortexes begin to appear and disappear in defect centers or pockets inside the crystal mass. These are the force field programmer vortexes from the higher dimensions. They will grow a seed crystal that has the ability to transform energy into force (bonding energy).
As the powerful rotating magnetic field of the magnetic rotator interacts with the stationary crystal, the lines of force are bent into the vortexal shapes, and helix crystals are grown quickly. These are only as large as DNA in diameter (30A), although much smaller in length, because they hold a much simpler programming.
In the growth process for the helix crystals, a mixture of different atoms is injected into the interface between the crystal mass and the magnetic rotator. This mix consists of anionic (negative valence) framework atoms, which are the raw material of the sheets, and a smaller proportion of diamagnetic atoms. These two types of atoms interact with the surface of the magnetic rotator, and the sheet materials form first. The hexagonal matrix of the ruby-garnet crystalline structure provides information that causes the sheet’s anions to mimic their structure, and the result is their reorganization from an amorphous mixture of anions into one that has the same symmetry as the layers of the crystal, that of a series of hexagonal layers that have tetrahedrally coordinated bonding between them. The anion sheets, however, do not have the strong tetrahedral bonds between their layers as do the layers in the solid garnet crystal of the rotator device.
During the growth process, the hexagonal sheets are folded over and compressed toward the tip of the vortex. The tip intersects with the magnetic quasi-crystal, which is the nucleator for the growth process. Between the magnetic atoms and the anionic sheets atoms, the spiral helix takes shape. Some diamagnetic atoms are also injected in the process, and these bond loosely into to sheets or spirals.
Helix crystal blends the qxtal symmetry with that of the hex and pent sheets. Long strings of atoms are laid out on a series of sheets that then twist or spiral in either a right or a left-handed direction. This structure is similar to that of an auger or screw. The strings are taken from both magnetic nucleator crystals and the sheet material. The former have a qxtal symmetry that is based upon dividing the circle up into even divisions that are multiples of five, while the latter are a series of crumpled hexs and pentas.
When these two forms interact, the twisted symmetry of the helix emerges. The strings that make up a single helix have elements of both qxtal and sheet symmetry. They appear only as linear strings, however, they are more, as the strings bond to one another in geometrical patterns that have a series of repetitive short-range orders (as in the sheets), but with no apparent long range ordering (like qxtals). These are the genetic code programmers that mimic conformation of nucleic acids in DNA helixes.
3. In step three, the spiral cells are collected and assembled into the light cells. Several of the cells are grown around a rare earth or alkaline dopant atom that acts as a nucleation site. The final metol cell array consists of four groups of atoms (similar to ATP molecule). 1. Anion sheets (ribose sugars); 2. Polyhedra magnetic atoms (adenine base); 3. Dopant nucleators (magnesium centers); 4. Diamagnetic atoms in veins or side chains (one, two, or three phosphates).
Light cells are similar to nucleus of a living cell. The many spiral unit cells are the DNA, the hex sheets are the ribose sugar molecules, the diamags are the phosphate molecules, and the dopants are the phosphorous atoms that link portions of the helix together. They are also similar to the cholesterol molecules, which have sugar-based side chains that spiral between molecules, and hexagonal bases that are composed of hydroxyl radicals, which have a negative (anionic) charge. These could be called “metal cholesterols,” or “metols” for short.
Light cells are grown in magnetic fields which align the spiral cells in a common axis that runs through the center of the light cells. In the growth process, the spiral cells are grown around the dopant atoms in the presence of a magnetic field that aligns all of the spirals into a common magnetic axis. Veins of diamagnetic atoms appear in these cells, and the dopant atoms luminesce vigorously.
These cells are egg-shaped as a result of growth process, which is like the solar wind process described. The spiral cells are injected into the b field along with sheet atoms, and the mix nucleates at the dopant sites. These cells grow quickly as the magnetic atoms spin in the b field, and sheet material is ejected from the surface of the cell until it is smooth or finished.
Like the nucleus of a cell, each light cell consists of several hundred spiral cell units, plus enough additional sheet material to make the final structure about 200A x 500A. These cells are composed of a large number of individual spiral cells that have bonded together into a spiral pattern. This, too, is like the cholesterol molecule, where individual molecules connect through the side chains to produce a molecular composite that has a spiraling geometry. While a single layer of fat molecules may only be, for instance, 20A in thickness, a cholesterol composite that is rotated through one complete turn will have a thickness of almost 1000A. This accounts for the considerable increase in size when the individual spiral cells aggregate into one composite light cell.
4. In step four, the light cells are assembled into the living cells, which are individual grains that are the size of a living cell, such as a blood cell (several microns in diameter). There is a major difference at this point between the shape of the cells in the body of an animal and these crystalline cells. While they are several microns in diameter, blood cells (and other types of cells as well) are only about one micron in thickness, thus presenting more of a pancake shape. The metol cells, however, have a more developed three-dimensional symmetry, and have the shape of a football. They have a thickness that is about one-half of their lengths. Technically, they would be described as ellipsoids with major axes of between 5 and 10 microns, and minor axes of about half their major axes.
Frequencies of sound and light are used to grow these large cells. Their diams are resonant to acoustical phonons with frequencies between .1 and 1 GHz. The corresponding EM frequencies of these phonons are in the ESR band of the cells. ESR is where the anionic sheets and the dopant center atoms come into resonance with each other in the presence of a magnetic field with a strength of 3000 to 5000 gauss. Frequencies of IR (heat) EMR that have wavelengths that are resonant to the grains are also used in the fabrication process. This radiation is circularly polarized during the growth process and the b field develops in an axis through the grain. This field is then rotated so that there are many magnetic axes, all pointing out from the center of the grains.
The magnetic field also is used to align the magnetic fields of the light cells that are on the surface of the grains such that these vectors are at right angles to the surface of the grains. Like the membrane of a cell, it superconducts. The light cell metols penetrate the membrane as it grows and, like cholesterol in a living cell, reprograms it with into a different form. This new form is that of the crumpled sheets.
The internal anion-cation electric field in the spiral cell ultimately produces the spiral form of the cell when it interacts with the spiraling electric and magnetic field vectors of the circularly polarized light that is used as a component of the crystal growth process. This light not only forms the spirals through electric field forces, but gives it programming as well.
The anion sheets are the raw material of the framework of the spiral cell. They are grown in specially shaped chambers that will allow a negative charge to develop in the framework atoms, instead of the normal positive charge. These sheets will develop a hexagonal symmetry if they are grown on a flat surface, but if a curved surface is used, the curved symmetry of the pentagon evolves, and this, too, is necessary for their refabrication into the geodesic form.
The exterior surface of the geodesic is composed of framework anions with the quadravalent charge of carbon or silicon. If these were the only atoms that were used in the construction of the spiral cell, then no spiral forms would develop, and the final form would not be much different from the forms of the known fullerene geodesics. But this is not the case, as additional sheets of cations are implanted into the geodesic in order to produce its final form.
The basic form of the spiral cell is that of the “infolded geodesic.” It is a normal geodesic on its exterior surface, but the interior has an additional spiral atomic form that occurs along what might be called its “central axis.” This axis is developed inside the geodesic when the magnetic field of the nucleating surface pulls the magnetic sheet atoms down into the interior of the anionic spiral cell.
The magnetic atoms are grown in a process that is similar to the one that is used to produce the anionic sheets, the difference being that the final product has a positive or cationic charge instead of a negative anionic charge. These sheets are then injected into the top of the anionic geodesic with a high velocity light beam. This beam not only provides the velocity (energy) that is necessary to implant the hexagonal sheets into the center of the spiral crystal but, by virtue of its circular polarization, rotates the magnetic implants as they are projected into the center of the geodesic crystal.
As the hexagonal sheets of magnetic atoms enter the geodesic, they are instantly slowed down by the friction that is encountered when they bounce off of the framework anions. But their forward travel is increased by the applied magnetic field, which is turned “on” in sync with the incoming beam of hexagonal matrix atoms. The force of magnetic attraction between the electromagnetic and the magnetic sheets pulls the sheets apart and converts their layered hexagonal form into a spiral hexagonal form. When the magnetic field is turned “off,” the magnetic atoms have been implanted into the central axis of the geodesic, and the final form of the crystal has been completed.
As the magnetic atoms are driven into the geodesic, they deform the top of the sphere into the anu form that is shown on the diagrams. As this is occurring, some of the magnetic sheets are bonded to the top most framework sheets, and the top of the spiral cell becomes magnetic. This magnetic field, however, is much weaker than the field that occurs along the spiral axis, as the axial field contains many more atoms than the top surface field.
7. PHYSICS OF METOLS
The magnetic atoms that are along the central axis form a small coil, and the top surface atoms extend it out of the cell as one end of the coil has a conical shape. This shape plays an important role in the operation of the spiral cell, as electrons that are trapped in the magnetic coil can be suddenly ejected out through the top of the cell along the path of these top surface magnetic atoms, and these electrons will superconduct when they are picked up by the superconducting sheets that constitute the membrane of the next largest crystal cell in this complex organization of material cells, the “Light Cell.”
The electrostatic field that exists between the anionic surface of the geodesic and the cationic magnetic spirals is considerable. With the application of the external magnetic field from the large coils in the craft’s electrical generator, the magnetic spiral atoms inside the geodesic are magnetized. This field places a large torque on the anions, as the alignment between magnetic and electric fields is always at right angles. This force would cause the geodesic to spin if it were not held rigidly in its lattice, but because it is, it is converted into a translational vibration that is carried by phonons throughout all of the spiral cells, and the larger organization of cells as well. In effect, each small cell acts as if it were a small hi-fi speaker, as it is deformed and pulsed by the application of the external electromagnetic fields.
One feature of the operation of the spiral cell is the production of phonons, and the other is the ejection of superconducting electrons. These electrons are supplied by the anions in the surface structure, and are accelerated out from the magnetic coil along a path of diamagnetic atoms that have been implanted into the top center area of the cell. These atoms, in turn, are loosely connected (bonded) to the superconducting sheet atoms, which occur in square matrix sheets of anions and diamagnetic atoms.
The electromagnetic principles of the superconducting electron ejection process are based upon the internal atomic “non-resonance” that develops between its microwave spin frequencies, which are produced by the electron’s magnetic spin energies, and by the higher visible and infrared frequencies of its valence and valence vibration spectra. The applied magnetic field excites the cell’s magnetic atoms to produce microwave spin frequencies, and the phonon action of the cell activates the valence spectra, and when the two come into a condition of non-resonance, energy is radiated rapidly away from them.
The term “nonresonance” is used to describe this, because the harmonic relationships between the lower spin frequencies and the higher valence frequencies do not occur in exact octave series. The frequency range between the two vibrations, one magnetic, as it occurs with the spinning electron, and the other electrical, as it occurs in the outer shells of adjacent atoms, encompasses between nine and eleven octaves, but there is not an exact octave relationship.
The energy that is expelled from the spiral cells has a dual, phonon-photon nature. The phonon energy becomes the kinetic energy of the superconducting electron that is ejected, and the photon energy is harmonically increased through the octave series until it produces a form of light that is currently unknown to science, that of “x-ray light.”
Spiral cells have nonlinear optical properties that extend into the tenth octave range. The valence vibration frequencies of the cell’s bonding electrons are the fundamental for the nonlinear series. This usually occurs in the near infrared. Ten octaves above this lies the x-ray spectrum. The cell emits a superconducting: [:sic- photon? photon? electron?] when the x-ray band is reached through harmonic generation, but the original structure of the photon is also preserved as an x-ray photon that has energy that is inversely proportional to the fundamental of the octave series that produced it.
The nature of nonlinear octave harmonics is such that while the frequency of the next highest harmonic is twice that of the previous one, the energy of this wave is one-half of the previous wave’s energy. A single spiral cell will emit a single photon whose energy conforms to this mathematical pattern, and it is, in effect, producing electromagnetic waves that do not follow the accepted (Plank) energy laws that state that as frequency increases, so does the energy by the same ratio. Harmonically generated photons have, instead, energy that is less by the inverse of the octave ratio.
When the upward nonlinear harmonics reach the x-ray frequency band, their energy per quanta has reached downward into the microwave bands, and non-resonance is able to transfer the microwave spin energy upward onto the ejected electron. It does this because it cannot transfer its energy onto the octave harmonic waves, as their quantum structure will not allow this to happen. The electron, however, is capable of absorbing energy on any level above a minimum (where it cannot exist as a particle), so the electron’s spin energy is transferred onto the superconducting electron, and this electron is able to superconduct through the conduction bands of the nonlinear material (the spiral cell).
The magnetic spiral cell is the most important unit cell structure in the composite materials that are used in the craft’s superconducting force field propulsion system. But there are other types of unit cells as well, and these, too, are vital to the operation of the craft.
The magnetic cell is the “firing superconductor,” or more correctly, “the firing cell of the superconducting sheets.” Before electrons can be superconducted at ambient temperatures, they must be programmed with a very wide band of conduction band frequencies. This can only occur in a unit cell that has the structural differentiation of the spiral cell. Each of the individual hexagonal and pentagonal units on the cell’s surface has a slightly different valence-to-conduction band series of frequencies that it can absorb and re-emit energy through. The spectra of these cells is like that found in molecules, where broad band absorption and transmission of frequencies occur, but with the structural differences between each of the cells, the bands are broadened even further until they encompass almost the entire infrared spectrum.
When an electron that is about to superconduct passes through the many different valence orbitals of the anions in the spiral cells, they pick up these energy levels and retain them when they are ejected from the cell into the superconducting square and cubic sheets. The conduction bands of the superconducting sheets are slightly different than those of the spiral cells, and the only way in which the superconducting electrons are able to adjust to them and superconduct at ambient temperatures is if they have already been in a valence-to-conduction orbital that has a similar energy level.
The unit spiral cells are the metols of the spacecraft materials. Their spiraling structures spin electrons out into the superconducting sheets, where they are accelerated to velocities beyond that of light, being converted into pure energy in the process. After these unit cells have been grown, several thousand of them are assembled into the “Light Cell.” This term is used because its size is in the range of wavelengths of the visible photons of light that are used to excite the spiral cells. This range of light wavelengths also includes the ultraviolet, which is shorter than the visible, so these cells can be between one-tenth and one-half micron in length and about half that in width, their shape being generally that of the ellipsoid.
In comparison, the spiral cells and their relatives, the lumino-diamagnetic cells, and the anion-cation structural cells, are all in the range of the size of the DNA molecule, being oblate spheres about 50A x 100A. Both of these cells are egg-shaped. The development of this shape is obvious in the spiral cell, as the implanting of the magnetic atoms deforms the spherical geodesics, elongating in the direction away from the ion beam and compressing it in the direction that the ions are coming from.
The light cells contain many thousands of diamagnetic-luminescence cells. The light output from these cells is considerably beyond any that can now be made. This is because of the much longer decay times for the photons that are undergoing luminescence than those that occur during normal phosphorescence or fluorescence. The luminescent atoms are also weakly magnetic, so when they are grown into their anion cells or cages, they are influenced by the magnetic field that is applied during the growth process. This field is rotated so that secondary magnetic fields occur at precise geometrical locations throughout the crystal. These locations then become the nucleation placement sites for the PL (paramagnetic-luminescent) atoms.
The PL cells have diamagnetic atoms throughout their structures. These occur at random locations because there is no way of using a magnetic field to control their growth morphology. Diamagnetic atoms are repelled by a magnetic field, and with many magnetic atoms inside these cells, they are pushed into random locations inside the cells. They are attracted to each other, however, and this attraction tends to organize them into a “veins” that are much like those that are found in the silica deposits of gold. These veins can be as small as one atom in width and as long as the entire cell length. Any diamagnetic atom that can be isolated into a single atom string is a perfect superconductor. This is one of the bases for superconduction in the Perovskite Superconductors, as the diamagnetic copper atoms are isolated by the crystalline lattice into sites that are connected by a series of square planes that are one atom in thickness.
The third component of the composite cell is added to the light cells for purposes of structural strength only. These are hexagonal-pentagonal sheets that have been grown into the long, twisting conformation of the body’s collagen molecules, which are the proteins that make up muscle tissue. This material is easily grown at any stage in the growth process of the light cells. It fills in the gaps between the other unit cells, and holds the light cells together. Long strings of these materials also occur between cells, helping hold the composite material of the craft together. They could be referred to as “metallic strings,” as they appear to be metal compounds that are woven together like thread or string.