pleiadian technology | book 2
1. METOL
The metol has the form of the “metal cholesterol.” It consists of two basic structures: one that is highly stable and precisely organized, and another that is unstable and is only loosely organized. The stable form carries the basic information that cannot be varied unless the entire form is altered, while the unstable form transmits the information that is contained in the stable form into other forms of matter (including those that are unrelated) that are part of the entire structure or “organism.”
The stable form of the metol consists of at least three quadrivalent atoms in an hexagonal array. The individual atoms in these arrays can be polarized magnetically to any level of gauss, while the hexagons can be polarized electrically to any level of charge. This allows for the storage of a wide variety of information in these magnetic and electric domains.
These structures mimic those of the cholesterol molecules which are found in all animals. These are the basic information carriers and information storage molecules for all of the biological molecules and biological structures in these bodies. Cholesterol molecules transfer subtle forms of information onto the molecular structure of newly forming cells, and in so doing alter the “subtle” properties of these cells. These properties include the way that they divide and grow, the way that they interact with the other biomolecules that are in the bloodstream, and their tendencies or capacities for pathological states. This is the long-range programming of the cell’s behavior in the biological system.
The cholesterol family of molecules, which includes sterols and steroids, consists of a group of three negatively charged hydroxyl radicals that are coordinated into a tetrahedral geometry. This geometry is portrayed in biochemical symbolism as a hexagon, this because the three dimensional tetrahedron is not easily displayed on the flat paper of textbooks. In addition to the three tetrahedron arrays, there is a single open tetrahedron that is portrayed as a pentagon. The pentagon designates that the end hexagon in the chain has a vacant site where a positive ion (usually a mineral salt, such as Sodium) can bond to the molecule.
The final structures in this family of molecules are the hydrocarbon side chains, which grow out from the open tetrahedral structure. These chains consist of hydrocarbon sugar molecules, which hold the opposite charge of the hydroxyl radicals that make up the main molecular body. Side chains grow in curves, and when two of these molecules bond together, their side chains cause the main bodies to align at an angle to one another. This alignment results in the rotational conformation of cholesterol structures. They also give these molecules the property of optical rotation, where light that is put through them is rotated as it interacts with the intermolecular alignments.
The tetrahedral array of molecular radicals in the cholesterol molecule is replaced by the hexagonal array in the metol cholesterol molecule. This array, however, is not perfectly flat, but has the form of the “buckled hexagon” of the water molecule. This buckled hexagonal array has the same form as the water molecules that are in proximity to it, and is the basis for the transfer of information from the metols to the biological molecules that make up all living things. If the buckled metols were folded in upon themselves to the maximum degree possible, they would be compressed into individual tetrahedron shapes.
The base atoms that make up the metol hexagons all contain slightly different levels of magnetic and electric charge, so- called dipole moments. These charges vary not just within each hexagonal array, but between arrays as well. Many arrays have identical charges, and these will transfer identical information into the biological molecules of the animals that are in resonance with, and in proximity to, the metols.
The hexagonal array of the metol is its fundamental or base line structure. These terms are used because this structure has a fundamental or base frequency of vibration that is determined by the velocity of sound as it moves around each of the individual hexagons in the hexagonal ring structure. There is one frequency for each side of member of the ring, another for each hexagon in the ring, and a third for the composite ring structure. This is identical to the translational vibrational bands of the water molecule, which consist of a base frequency that is the velocity of sound along one side or leg of the water tetrahedron (or water hexagon), and other frequencies that are this same velocity along two, three, of four sides of the water molecule’s structures.
The phonon interactions and harmonics of the metol molecule mimic those of the water molecule. Many types of information can be transferred from the metols to the water molecules of the animal body, affecting that body in a wide variety of ways.
The unstable portion of the metol is that of its side chains, which are polarized oppositely to the hexagonal chains, and which also grow into the form of a spiral. The metol side chains mimic those of the cholesterol molecule, which are also curved into spirals.
The side chains are the dynamic portion of the metols. They bend the hexagon chain’s phonon vibrations into circular waveforms that then are then broadcast into the USC (unit spiral cell) from the cell wall or perimeter. This occurs in living cells when the cholesterol molecules in the cell’s membrane broadcast information into its interior. The side chains twist the waves into a form that can only be duplicated when a sound wave undergoes superlaminar flow at the speed of sound, At this velocity, sound waves begin to experience an orthogonal force that twists them into small vortexal shapes. It is these vortexes that move information up from the third into the fourth dimension.
Between the hexagons and the side chains are the transition elements of the metols and cholesterols. These are the single pentagons in the metols, and the open hexagons in the cholesterols. In the metols, the pentagons bend the base form into a curvature. If there are twelve pentagons in the metol structure, then the curvature is completed into the form of a structure that can be enclosed completely by a sphere. This number of pentagons can also be used to make any of the known Fuller Geodesic solids, which are based on variations in the icosahedron or dodecahedron.
In the cholesterol molecule, the open site on the last tetrahedron causes the molecule to take on a curved shape. When the side chains grow out from the cholesterol molecule, they, too, follow the curve that has been established by the open tetrahedron. This is where the cholesterol molecule is closest to the metol in its conformation. The pentagon in the metols causes its side chains to curve out into the space around it.
In the cholesterols and sterols, the side chains disrupt what would be an otherwise perfect unit cell lattice structure, and extend the size of the unit cell to include one complete rotation of a large group of molecules. This is the reason that cholesterol molecules come in thicknesses that are as large as 100 nm, while the individual molecules themselves are less than 1 nm in their length.
In the metols, the side chains extend the size of the unit cell from that of the simple cube that is based upon a group of eight geodesics, to the size of the unit spiral cell, which is much larger. The USCs are over 100 nm in length, where the individual geodesic metols are only about 1.5 nm in length. In both of these forms, the simple cubic lattice structure is disrupted by the side chains so that all the individual geodesic crystals are no longer in a rigid lattice structure that has three orthogonal axes. Instead, each geodesic grows at a slight angle to its main axis, and if this angle can be preserved throughout the macro crystal, its final growth form, the USC, will have a rotation to it lattice structure.
Each USC has several complete rotations for its individual geodesic crystals, and it is this rotation that defines the limits of its structure, as these cells are grown in the presence of sound and light waves that have quarter, half, and whole wavelength resonances to the lengths of the USCs. These cells grow into the natural form of the egg, as the direction of propagation for the waves pushes its bottom outward, while the natural sine wave amplitude pushes out its sides.
The latest notes on the metols were derived from calculations which showed that the FIR translational bands for the unit cell metol is in the same range as that of the water molecule, but possibly extended from 5-60 cm-1. Taking the speed of sound through the metol at approx. 6,000 m/s (it could be higher), and assuming that each cell is resonant to a wavelength of half wavelength of its own t-band energy, the size of the cell works out to be about 30-60 Angs.
In cholesterols, the positive side chains bond with the water molecule, and so they are referred to as the “hydrophilic” portion of the molecule. The polygon body portion of the molecule holds a net negative charge and will not bond with water, and so is referred to as being “hydrophobic”. In the metols, the polygon bodies have the same negative charge, and the spiral side chains a positive charge.
The positive side chains of the cholesterol molecule are sugars, which are soluble in water, hence the designation “hydrophilic”. Sugars are high energy molecules which are absorbed by the brain cells whenever they are doing their work. In the metols there are no direct analogies to these sugars. Instead, the positive side chains are made up of a nearly equal balance of magnetic and diamagnetic atoms. These function in pairs to accelerate electrons along the surfaces of the LCCs [living crystal cells] until they are able to superconduct. The LCC is the cellular for of the metols.
In cholesterol, the side chain sugars are rotated. This is unlike the phospholipid (fat) molecules, where the side chains are straight. The side chain of one cholesterol molecule does not bond to the side chain of the next or adjacent molecule, but instead lies parallel to it. When fat and cholesterol molecules lie next to one another in a membrane structure, the sugar molecules of one chain fit into the openings between the sugar molecules in the next chain. In the fat molecules, which are not rotated, this produces sheets of molecules that only have the thickness of a single molecule, about 20A (Angstroms). In cholesterol, however, the side chain sugars are rotated from one chain to another, and this produces a structure that has the thickness of as many as 50 molecules, or about 1,000A.
The side chain rotation of the cholesterol family of molecules occurs because of very weak surface forces that are different from those that occur in the linear fat molecules. These forces are produced when electromagnetic radiation is rotated by the spiral chains. This rotation changes the electric and magnetic fields of the radiation so that they do not completely cancel between their positive and negative amplitudes, and these fields attract the side chain sugar radicals to each other. This attraction is weak, but it is sufficient to hold adjacent chains together in the supermolecular configuration of the cholesterol membrane.
The feature of optical rotation also occurs in the metols. When a side chain bonds to the polygons above or below it in the cell, they rotate it into a slightly different position relative to itself, and when they bond to the next layer of polygons another rotation occurs, and so on throughout the entire layered structure.
Magnetic and diamagnetic atoms are implanted on the surfaces of the light cells, and when this occurs, a small depression in the surface features occurs. Electrons, which have now become the equivalent of the water molecule’s negative hydroxyl ion, are trapped in the magnetic holes and circulated back and forth between holes that are on the surfaces of adjacent and facing cells. This amounts to a double vortex action with the electron being bounced back and forth between cells and vortexes. They also will migrate between cells during this action.
As electrons move up and down the surface vortexes, much as they move in the Earth’s Van Allen Belts, their velocities increase. Eventually, as they bounce between magnetic vortexes, they will encounter a diamagnetic formation, that is, a collection of randomly oriented diamagnetic atoms that have also been implanted into the surface of the cells. When this happens, the electrons are suddenly subjected to an opposite or diamagnetic field, and this causes them to leave the spiral paths of the twin vortexes (vortex pairs) and superconduct along the path(s) of the diamagnetic atoms. This entire process has been described in terms of the “firing superconductor.”
If a string of diamagnetic atoms that is one atom wide were to be constructed, perfect superconduction at any temperature could occur. But this seldom occurs, and instead, the diamagnetic implants into the spiral cells are usually a few atoms in width. This produces eddy currents and electrical resistance as they move between atoms, but these are still excellent conductors. The diamagnetic paths through the light cells connect together with other paths, and electrons are conducted into the superconducting sheets that are grown onto the surfaces of the final metol form, which is an unlimited number of adjacent light cells.
The surface of a single spiral cell is made up from many basic unit cell polygons that have a negative charge. These are composed of framework atoms that have been converted from cations into anions. The conformation of the unit cells is such that they never form a completed structure. This makes them entirely unlike the existing sulelrene [sic fullerene] type of crystals, but exactly like biological molecules, which form a series of potentially infinite chains, as exhibited in such forms as the collagen proteins that form into muscle tissue, or the hexa and hemicellulose chains of plants, such as those that are made into string and twine (the hemp plant).
With a never ending structure, how do these form into single spiral cells? The answer lies in the same formative processes of nature that produce three dimensional crystals, such as quartz or calcite. Each group of polygons, which can be considered to be a single molecule, is grown into a series of parallel layers that have a rotation between layers. In quartz this is known as “optical rotation.” This conformation also occurs in many types of biological molecules.
If this type of growth conformation can be developed, the spiral cell will develop and the succeeding stages will also be successful. Each layer is bonded to its adjacent layers by its magnetic and diamagnetic side chain atoms, which give the layer a small twist before it bonds to the next layer. At the perimeter of the cell, the side chains are bent over so that a pseudo surface is formed. This term is used because although it is in reality a real surface, it is composed of a combination of side chain atoms and polygon atoms. The former are only loosely bonded to the mainframe polygons, and so the surface of the USC has a different morphology than its interior. The surface area interfaces with superconducting materials. These have been grown in a separate process and they are mixed in with the USCs when the next largest cell is grown, the Light Cell.
The side chains of biological molecules, such as cholesterol, cause chains of these molecules to rotate.
The USCs are grown in the magnetic arc process that was described previously. This process produces fairly uniform single crystals that have a spherical or ellipsoidal shape. These crystals are nucleated around dopant atoms, which remain as positive charge centers inside. The USCs are so small that they spontaneously come together to form the Light Cell. They only remain separated in the growth process, which spins them with so much energy that they form individual surfaces. As soon as they cool down, they clump together into the Light Cell Crystals. During this cooling process, small amounts of superconducting material are added to the USCs, and this immediately sticks to their surfaces and fills in the space between them as they aggregate into the Light Cells.
Spiral cells have a size that is variable, but dependent upon the relationship between the translational vibrational bands of the unit spiral cell and the size of that cell as a resonant unit, this size being defined as the velocity of sound over its surface in a circular and repeating pattern. As the calculations turn out, this limits the size parameters of the spiral cell to between 30 and 60 Angs.
Light Cell Crystals or Living Crystal Cells (LCCs) are the equivalent of a single living cell in a biological organism. They range in size from one to ten microns in length and about half of this dimension in width. This is a combinational cell that is composed mainly of USCs, however, the specially grown superconducting sheet materials are mixed in. The superconducting sheets stick to the surfaces of the many thousands of USCs that make up the LCC. They are the cell membrane material. They are composed of alternating anion sheets (with diamagnetic centers) and cation sheets. They have a cubic lattice structure, superconducting square planes, and an overall morphology that is close to that of the known high temperature superconductors.
In the final growth process, the surfaces of the LCCs are implanted with magnetic atoms that produce the magnetic vortex centers. These centers are the “firing superconductors” for the craft’s electrical system. The LCC is the basic unit cell for the construction of spacecraft or similar structures. Large numbers of these are grown along with additional superconducting material into the hull structures of these craft. Sometimes in the growth process, many LCCs will become stuck together. If this happens, the clump of cells is grown together with other clumps into a final structural form. These clumps lessen the superconduction of electrons through the structural forms, and if there are too many of them present in the final structural forms, they must be disassembled through ion beam bombardment. If this is done carefully and at the correct energy levels, the individual cells are not destroyed.
The spacecraft metols are configured similar to the organic cholesterol molecule. The polygons in cholesterol (usually three hexagons and one pentagon) have a net negative charge because of their numerous hydroxyl radicals. These structures occur in the buckled conformation of all biological molecules. Instead of being arranged in a lattice structure that is planar and two dimensional, they are arranged in a three dimensional lattice that moves up and down around its circumference. This is similar to the lattice structure that is found for solid (frozen) water and quartz, which have their molecules arranged in puckered hexagons, also known as “hexagonal rings.”
In ice and quartz, the buckled hexagons occur in layers that are coordinated or bonded together by tetrahedrons. This is a three dimensional polyhedron with four sides and four points. It is the only polyhedron that has an equal number of sides and points.
In molecules or crystals that have tetrahedral coordination, one molecule is located at each point. In the case of ice and quartz, the tetrahedra can coordinate as many as three adjacent hexagonal rings by having two molecules in one ring and one molecule each in the ring above and one in the ring below.
More commonly in ice, only two rings are coordinated with three molecules in one ring and one in the adjacent ring. This is the usual form for ice, which grows (freezes) in sheets that do not have tetrahedral bonds to the sheets above or below. If, however, ice is quick frozen or frozen under pressure, as occurs in glaciers, this bonding pattern will be altered, and the result will be the formation of blocks of ice that are stronger than the layered ice. The rings in these blocks would have the same tetrahedral coordination as the Silicon Dioxide molecules that make up quartz.
When a metal is transformed into a “metol,” it is given a structure that is similar to that of quartz and ice. It is ordered into layers of buckled hexagonal sheets that have tetrahedral coordinations between them. In addition, pentagons are grown into the sheets, something that does not occur in ice and quartz. These give the sheets a curved instead of a flat structure. The curves eventually can bend a chain of metol molecules into a structure that is similar to a Fullerene, which has the geometry of a geodesic sphere or ellipsoid. Because of the importance of the geometry of the sheets that compose a portion of the composite metols, they will be given the abbreviated name of “hexapent” sheets, which means “hexagonal-pentagonal” sheets.
The object in growing metols is to not allow them to buckle too much and fold over on themselves and complete their structures into a Fuller geodesic. If this happens, the flow of photons and electrons through the metols will be interrupted, as they must, in effect, jump to the next complete structure before resuming their journey through the larger collection of structures. This jump requires energy, which is converted into heat, and which, in turn, is useless in producing the desired force field effects of the craft.
Metols consist of two basic type of structures, “cellular” and “membrane.” The former is the main body of the grains that are pressed together into the final structure. These are equivalent to the protein peptide and collagen chains that form the bulk matter of living cells in animals.
Membranes are the superconducting square and cubic lattice structures of metols that are coated or grown onto the surfaces of the cellular grains. These are grown as the hexapent sheets are implanted with magnetic and diamagnetic atoms. The diamagnetic atoms transform the hexapent lattice structure into a square plane lattice structure, similar to the square planes arrangements that are found in the Perovskite family of superconducting ceramic polycrystals, and the magnetic atoms further transform it into a three dimensional cubic lattice structure.
The metols are arrayed onto the surface of the LCC. The LCCs are much larger structures that consist of hexapents that are both positive and negative, and rare earth cation dopants that are added so that ESR can occur in the structure, and so that luminescence will be increased. The LCC geometry and conformation looks like a ball of string or a plate of spaghetti. Hexapent after hexapent is folded through, over, and around each other as the structure is tied together into a form that is virtually indestructible. Negative structures predominate, although positive ones also are grown in, and the cation dopants play the important role of providing all of these negative structures with a positive bonding site. Only on the surface of the LCC is order re-established in the almost perfect symmetry of the metols and superconducting sheets.
On the surface of the LCCs, the metols are arranged with their positive side chain geodesics perpendicular to the surface of the cells. The superconducting sheets, which consist of diamagnetic atoms and framework atoms in a square plane matrix, are interpenetrated at right angles by the side chains of the metols. The metols act as the firing superconductors for the superconducting sheets, ejecting electrons into the sheets for superconduction.
Another group of magnetic side chains has a cubic relationship to one another. This develops naturally as magnetic atoms, such as iron or nickel, are implanted into their hexapent (hexagonal-pentagonal) structures. This converts them into a square plane layers that will further self-organize into cubic structures. The magnetic group is used as a “firing superconductor.” Electrons are trapped into magnetic vortexes, then accelerated up and down their lengths in spiral patterns, and then, when the magnetic is suddenly reversed, are ejected out into the superconducting diamagnetic metols and superconducting sheets.
Dopant implants atoms serve two purposes in the metols: they program the positive geodesic side chains into either superconducting or supermagnetic structures, and they program the negative polygon sheets into superluminescent crystals. In the case of the latter, the positive charges of the dopants also hold the negative sheets together by electrostatic attraction. Ordinarily, they would be repelled by their like negative charges, but the presence of a positively charged ion provides them with a common bonding site.
The magnetic dopants’ atoms can be any ferromagnetic or paramagnetic atoms, and the diamagnetic dopants can be any diamagnetic atoms. The luminescence dopants in the sheets are usually specific cations in the alkaline metal or rare earth categories of the Periodic Chart. The superconducting sheets are grown perpendicular to the direction of the metol strings. They are centered by the diamagnetic atom at the center of the positive geodesic, which is also located at the corners of the cubic lattice structure that exists between all of the metols that make up the next largest structure member in the material, the Living Crystal Cell.
Only the surfaces of the living crystal cells have metols. The interior of these cells is composed mostly of a combination of negative and positive sheet polygons that mimic the conformation of protein peptide chains in the cells of animals. These structures are used primarily to build up the internal structural strength of the cell, as this is an important factor in the operation of spacecraft. They amount to a metallic fiber that is woven throughout the structural members of the craft in order to give it structural strength.
It is one thing to develop a force field, but it is quite another to be able to hold the craft together as the field is operating.
2. METOLS AS FULLERENES
Fullerenes have a small net positive charge to their structures. In the well-known Carbon Bucky Balls, the normal carbon radius of 1.54 A is contracted to 1.45 A. This means that their net charge is now slightly positive. The structure has not lost an entire electron per atom, as this would have contracted it to a much smaller size than has been measured, but a small number of electrons (as many as five) have been lost to the entire structure of 60 atoms. For this reason, the contraction of the C60 molecule is much less than it would be if all 60 Carbon atoms lost one electron each.
The surface of a Fullerene can be thought of as a pseudo electron orbital that is capable of absorbing a large number of excess electrons. These extra electrons will give the overall structure a net negative charge, however, the electrons are not in true atomic orbitals, and so the energy that is required to remove them from the surface is small when compared with the energy that would be required to remove them from an atomic orbital.
The production of positively charged Fullerenes is simple. It only requires heating the atoms into the vapor state. In this state they lose some of their outer electrons and the mass of atoms take on a positive net charge. Actually, these electrons are continually coming onto the outer shells of the atoms and then leaving again through ionization. When they leave the atoms, they have a net positive charge, and when they return, a net negative charge. When heated to the vapor point, a group of atoms will always take on a net positive charge. This is because their intrinsic energies are so great that their outer electrons cannot remain bound to them.
When the heat is removed from the mass of atoms they then will come together into the C60 structure. The structure will have a net positive charge, because the electrons that have been lost will not be regained before the atoms have cooled into their new structures.
Metols differ considerably from the known Fullerenes in two principal ways: 1.) They have heavy metal atoms in their framework instead of Carbon, and 2.) They are grown into a “negative conformation,” with negative net charge, and open instead of closed surfaces. This makes them much more difficult to grow than the Fullerenes.
The conformation of a geodesic molecule, whether it is a Fullerene, organic molecule, or metol, is based upon a correspondence between charge and geometry. A positive structure will have a “positive” geometry, that is, one that folds over on itself or completes itself in space. The known family of Fullerene geodesic molecules are positive structures. A negative structure, on the other hand, not only has a net negative charge to its atomic structure, but a “negative” curvature in space as well.
This curvature prevents successive chains of molecules from ever terminating in spherical structures. This structural conformation occurs in all protein molecules, which consist of chains of smaller molecules. These chains are potentially infinite in terms of their mathematical structure. The DNA molecule, for instance, is the largest known molecule. There are twenty individual amino acids which are used over and over again in sequences that never repeat.
The metols repeat the conformation and structure of protein molecules and protein peptide chains. There are only a relatively small number of possible molecular forms, but they are organized into sequences that are virtually infinite in their possibilities.
Metols also have the same structure as the cholesterol molecules that are found in the membranes of the living cells of all animals. They are grown perpendicular to the cell membrane and interpenetrate its structure. Again this occurs in the living cells of animals, where the cholesterol molecules penetrate into and through the phospholipids that make up cell membranes.
In order to grow a metol, the hexapent arrays of atoms must take on a net negative charge in their lowest energy states. This means that they cannot be grown in a vapor process, as this would only produce positive structures, such as the Fullerenes.
Metols can only be grown in cold fusion process where they are heated up gradually in the presence of excess electrons. When they are properly grown, negative sheets of pentagons and hexagons develop, but unlike the fullerenes, they do not fold over on themselves and produce a closed, positive structure.
The negative hexapent sheets of the metols are grown in a “cold acid arcing” process. This process uses a high voltage arc, which develops little heat, to slowly energize and expand a sheet of atoms. Together with ultrasonic waves, these atoms are slowly rearranged into the hexapent polygons of their intermediate structures. After the sheets have been grown, they are removed from the growth chambers and prepared for the second growth stage.
The second growth stage for the metols develops their biological or living conformation. In terms of their geometry, this means that the hexapent sheets are buckled into a number of different directions and bent into a variety of shapes. This is only part of the change that occurs during the conformational process. The most important is one that involves a reprogramming of the outer electron orbitals so that each sequence of hexapent metols has a slightly different level of negative charge. This changes the buckling angles of the polygons, and the hexapent angles around the perimeter of the chains. These physical parameters determine what types of dopant atoms the chains are most suited to bond to, and therefore what types of dopants can be added to what types of chains.
Hexapent sheets have tetrahedron bonds between them. This makes them similar to ice, the difference being that there are many more bonding possibilities in metols than in water and ice. Usually, each atom in a metol has this bonding geometry with two other atoms in its own polygon, and with one atom in each of two other polygons. This occurs in quartz, but only occurs in certain types of ice. Usually ice is limited to only two tetrahedrons per hexagonal ring, and quartz to three. The metols, however, are not so restricted and can have as many as six tetrahedra per hexapent ring. This makes the bonding strength of the metols considerably greater than that of ice or quartz.
The third stage process is where the final metol is grown. It involves the brief vaporization of the hexapent sheets in an electric arc that is controlled by a direct magnetic field. The magnetic field forces the negative ions in the sheets to rotate into sheets that are expanded into a greater negative valence on one end and contracted into a positive valence on the opposite end. The negative charging occurs as the sheets move into the central portion of the magnetic field, where the field strength is the least, and the positive valence and compression of the sheets occurs towards the magnetic poles, where the field strength is at a maximum.
When the metols are finished in the third stage, they exhibit the structure and conformation of the cholesterol molecule. They have vast arrays of negative sheets that are attached to small, compressed side chains. Toward the magnetic poles, the sheets are compressed and wrapped into a structure that is very different from the negative sheet arrays. As the field pinches the sheets, the polygons break down completely, and only the tetrahedron bonds remain. These are spinning rapidly in the magnetic field, which reorganizes them into a series of spirals.
The material that develops spiraling “cholesterol” tetrahedrons has been doped with diamagnetic atoms. This is usually done before the process is initiated. Diamagnetic atoms are strongly repulsed by a magnetic field, and the ones that are doped into the hexapent sheets are no exception to this rule. As the sheets approach the magnetic pole, they are wrapped around each other in ever tighter patterns. But the diamagnetic atoms are repulsed by the field and begin to move in the opposite direction. They pull themselves free from the sheets and reform into tetrahedrons with sheet atoms at their centers and diamagnetic atoms at the points.
The side chains of the metols are the same as the side chains of cholesterol. In cholesterol, the sugar molecules that make up the side chains are rotated at specific angles with respect to each other as one moves down the length of the chain. If the side chains in one cholesterol molecule tie up to those in a second cholesterol molecule, then the second molecule will be rotated with respect to the first. This rotation occurs throughout an entire chain of molecules, and gives them the property of optical rotation, that is, the ability to rotate any photons of light that are put through them.
During the magnetic arc processing, the sheets are compressed and rotated as they approach the magnetic poles. This rearranges their lattice structure from one that is dominated by polygons to one that consists only of tetrahedrons. These are the remnants of the tetrahedron bonds that occur between the polygon sheets. The polygons have weaker internal bonds than the external ones that occur between the layers. When the force of compression breaks apart the polygon structures, the only bonds remaining are the tetrahedrons.
In the side chains, there are three possible bonding configurations for the tetrahedra. One is a tetrahedron that has dopant atoms, either paramagnetic or diamagnetic, at its points, with one framework atom at its center. Because of the bonding forces that would be required to rearrange the tetrahedra so that the framework atoms occurred at the centers instead of at the points, this is not a likely formation. It is more likely that the tetrahedrons retain the polygon framework atoms at their points and add cation dopant atoms at their centers, with magnetic or diamagnetic atoms loosely bonded onto the outside of each of the polyhedrons. (number 2 possibly).
The third configuration involves the doping of atoms into the sheets before they are subjected to the magnetic arc process. In this process, a dopant atom is substituted for a framework atom in the hexapent framework, and the new framework is a composite of framework atoms and dopant atoms.
Some atoms are much more readily doped into the polygons than others. Which ones are most easily substituted depends upon how similar they are to the framework atoms in their possible ionization states. The framework atoms usually can ionize two, three, or four electrons. If the dopant atoms can also ionize these numbers of electrons, then their substitution into the latticework is easily accomplished. However, only certain atoms have this ionization configuration. The strongest magnetic atoms from the ferromagnetic group are Iron, Nickel, and Cobalt. They are able to ionize two or three electrons but not four, so they are as easily substituted into the polygon framework as are other atoms.
The strongest diamagnetic atoms are also the best conductors. These are Copper, Silver, and Gold. These atoms will only ionize one or two electrons, and so they are the least compatible with the framework atoms, and the most difficult to substitute for them in the polygons. Usually, these atoms can only be added onto the tetrahedra as loosely bonded exterior atoms, much as the element Hydrogen can be added onto the exterior of many types of organic molecules.
The bonding rules that are derived from the ionization levels of the various dopant atoms determine the composition and structure of the individual tetrahedrons that make up the side chains in the metols. If the three possible electron ionization configurations for the different dopants are designated as “Groups II, III, and IV,” then their relationship to the three possible types of tetrahedrons can be defined in general terms.
IV Group dopant atoms are those with the same “1-2-3-4” ionization sequence as the framework atoms. These include all atoms that can lose up to four electrons through ionization. These atoms need not have the preferred ionization sequence of “1-2-3-4.” They can have any of the following sequences: “1-2-4,” “1-3-4,” “2-3-4,” or “3-4.” Framework atoms are from this group, so these atoms are easily substituted for framework atoms in the metol sheets and tetrahedron side chains.
III Group dopant atoms are those with the “1-2-3” ionization sequence. These atoms form cubic lattice structures. When they occur in the side chains, they organize successive chains into a body-centered cubic symmetry. This symmetry also occurs in the superconducting sheets, and the two merge into a single structure at right angles to one another when the latter is in the process of forming from the former. This group of atoms includes the highly magnetic ferromagnetic atoms Iron, Nickel, and Cobalt.
II Group atoms are those with the “1-2” ionization sequence. These are the diamagnetic atoms, and they are the least compatible with the “2-3-4” framework atoms. Usually they are only able to join with them in square plane lattice structures.
This configuration occurs when the side chains are making their transition from being metols to being superconducting sheets. In the latter, square plane arrangements of atoms occur. These planes are connected by vertical tetrahedron bonds that have II Group atoms at their corners.
In the interface between the II and III Group portions of the side chains, diamagnetic atoms begin to occur between groups of paramagnetic and ferromagnetic atoms. This is the configuration of the firing superconductor. Electrons become trapped briefly between the magnetic atoms, and when there are polarity reversals in the magnetic field, or a sudden collapse of the magnetic field, they are ejected from their traps. They are immediately captured by a diamagnetic atom, which superconducts them onto the superconducting square planes.
Once in these planes, they are transmitted almost instantly to all of the other metols and LCCs in the entire composite structure. With the phenomenon of the “speed of light” transmission of electrons and simultaneous production of luminescence photons, the force field is built up simultaneously at all locations about the structure and remains uniform. If these events were not simultaneous, or nearly so, the force field would be out-of-sync with itself and it would have a wobble or precession that would make it useless as lifting force.
3. SUPERCONDUCTIVITY IN METOLS
The negatively charged polygon sheets have holes in them. Cations are able to move through them. Metol chains are arranged perpendicular to the superconducting sheets, and when electrons conduct in one direction in the square planes, cations move in the opposite direction. When the sheets are grown, the diamagnetic dopant atoms are loosely arranged through the centers of these holes to form veins or strings in the material. These carry the electrons in their initial or firing stage.
Hydrogen atoms also move through these holes during the operation of the craft. In fact, these atoms are the only fuel (if that term can be used) that the craft consumes. Usually it is able to pick up this fuel when it moves through clouds of protons and electrons in outer space, such as the Van Allen Rad Belts. When operating in an atmosphere, other atoms are substituted for hydrogen as a positive charge source.
As electrons superconduct in one direction around the hull of the craft, either clockwise or counterclockwise, the cations move in the opposite direction. Their movement occurs at sonic velocities while the movement of the electrons is at light velocities.
The coordinated movement of cations or protons in one direction and electrons in another is paralleled by the back-and-forth movement of phonon wave trains. These are also known as solitons. Low frequency phonons move with the cations or protons and an extremely high frequency phonon moves with the electrons.
When these waves reach either the center of the craft or its perimeter, they are reflected back toward each with a reversed polarity current. The reflected current consists of electrons that move in toward the center and protons that move out toward the perimeter, but because of the slow speed of the latter, the current does not go very far before it is met by the next wave of superconducting electrons, which push it back toward the center of the craft. The positively charged cations and protons are never able to make it out to the rim of the craft, and there is always a negative bias in this direction and a positive in the other.
The overall result of these currents is a net current that is always negative toward the outside, and positive toward the center. Protons accumulate at the center of the craft and electrons on the rim. This duplicates the structure of an atom. This structure is necessary for the production of the craft’s gravitational force field. This field must operate across the entire radius of the craft if there is to be any lift. Small, individual force fields are not adequate for lifting a craft, as their distance of action is too small. They must be reorganized into a large central force that acts through a large radius.
The weak nuclear force that is used to lift the craft against gravity, or more correctly, to develop its own gravity, could be produced by the decay of a gamma ray into a positron-electron pair. This is one of the most fundamental and prevalent of reactions that occurs in the particle accelerator experiments of high energy physics.
In the experiments of high energy physics, powerful magnetic fields and high potential electric fields are used to accelerate particles in a vacuum up to the speed of light in velocity. They are then deflected in their paths so that they collide violently with atomic nuclei. The result of this is the disintegration of the nuclei into many particles that have the property of “mass-energy,” that is, the masses and energies of these particles are mutually convertible or the same thing. If energy is put into these reactions, it usually is converted into mass in the form of particles that are heavier than the atom’s protons and neutrons. These heavy particles will quickly decay (break apart) into smaller particles until a stable collection of particles has been reached. This occurs in a very short period of time (in the range of a few millionths of a second), depending upon what type of particles are occurring in the decay scheme of the original collision.
Gamma rays are always emitted in large numbers during nuclear reactions. This is true for nuclear reactors, nuclear bombs, and high energy collisions. This ray is more energetic than x-rays, and it decays into one electron and one positron plus a small amount of nuclear force, also referred to as the electroweak force, because it is associated with the electromagnetic gamma ray. If a large and coherent source of gamma rays could be found, it could be harnessed into a force field to lift a vehicle of some type. Unfortunately, the energy requirements of such a craft would make it impractical. The radiation alone would be highly dangerous.
Instead of using the gamma decay force, these spacecraft use the lower level forces that develop naturally in organic molecules. The compression and rotation of light waves in chains of these molecules produce solitons and a covalent force field. There is little danger from radiation, as the energy levels are kept in ranges that are compatible with the operation of atoms and molecules, only a few volts per particles.
The reaction that produces the covalent force field is much more complex than the one that produces gamma decay in a nuclear event. It combines photons with phonons in a complex wave pulse through a superconductor that is unlike any that are known, excepting those that have been observed to occur in biological molecules. In these reactions that produce the covalent force field, electrons spiral out to the rim of the ship’s structure as protons move inward.
The metol sheets have a negative valence charge which means that they attract positive charges. The cations are easily bonded between the negative sheets, making cages similar to the Crypt and Cages that occur in the ether family of organic molecules. These structures never complete themselves and are potentially infinite in size although, as a matter of practical occurrence, are limited in size to about 30A x 50A, with a thickness of approximately two atoms.
The sheets are parallel to one another. As they curve slightly, they define the surface of the LCC, which curves over on itself until it forms into the shape of an ellipsoid. The LCC has the structure of an onion. It is composed of a series of parallel and curved layers of negative valence framework atoms. The cations that occur in between the sheets have their analogy in the seeds of the onion, which are scattered throughout its layered structure, but which also occur in their greatest numbers at the center of the onion. This too occurs in the LCC, as the center of the ellipsoid has a large number of cations that are in the structure of the quasicrystal.
The two-atom thickness of the sheets occurs because of the crumpled conformation of the sheets. This pushes some atoms up slightly and others down slightly. The sheets make a series of cages that are held together by the cation dopant atoms, which can be very numerous. The greater their number, the greater is the bonding between the sheets. These atoms produce a high degree of luminescence when they are bombarded by the free electrons that leak out from the craft’s electrical current. The frequencies of this luminescence are the ones that are seen when these craft operate at night.
Voltage to amperage conversion takes place in the superluminal pyramids of the superconductor. [Illustrate with YBaCuO.][sic]
The side chains of the metols have a net positive charge and structure. They are a series of Bucky Fullerene crystals with either a dodecahedron, icosahedron, or icosa-dodecahedron (Fullerene) symmetry. When the basic raw material of the metols, the hexapent sheets, are processed through the magnetic arc growing unit, these crystals are spun into their final conformation, which is a series of spiral chains. These mimic the conformation of the sugar side chains of the cholesterol molecule, which are arranged in a spiral. This spiral rotates this organic molecule so that when light is put through it, an optical rotation occurs.
The spiral side chains play a vital role in the operation of the craft. They rotate the light that is emitted during the luminescence of the cations. The rotated light is then compressed through the spiral implants in the LCCs, and this compression produces the force field of the craft.
The spiral side chains have a net positive charge to their structure. They therefore attract large numbers of electrons, which are supplied by the superconducting current that moves through the square plane membrane sheets. These electrons aggregate on the surface of the metol ions, and they increase the friction between these structures and the superconducting electrons. This friction creates a force which pulls on the side chains until they vibrate violently, producing frequencies of sonic energy. This sonic energy is used to increase the energy levels of the much higher frequency (shorter wavelength) phonons that act as wave guides for the superconducting current. Without this acoustic energy, there would not be enough phonon energy to produce an adequate wave guide.
The spiral implants occur on the surface of the LCCs. When magnetic atoms are implanted into the LCCs, they produce surface deformations that have the shapes of cones or vortexes. The magnetic atoms are implanted by ion beam equipment that accelerates Fullerene crystals into the surface of the LCC. Their energy is sufficient only to penetrate the surface to a small depth. While moving through the hexapent sheets, the implants interact with them to convert them into a “square matrix spiral” form. (DIAGRAM HERE OF 5-4 SPIRALS) [sic] This spiral form has the very unusual properties of the DNA molecules of the body. It rotates and compresses the light so that in the process of frequency shifting through valence-to-conduction, it converts some of its energy into a force field that acts through a distance.
The diamagnetic atoms that are found in the positive side chains of the metols are in one of two conditions. A small number of them, usually 1-3, locate at the center of each of the Fullerene Crystals, with the larger geodesic holding more atoms than the smallest. The atoms that would normally bond onto the surface of the geodesic cannot do so because of its net positive charge, (the diamagnetic atoms also have a positive charge) and because there is not enough space between the framework atoms in these structures, the positive structures being smaller than the negative ones. The atoms that cannot locate on the surface of a Fullerene or inside it usually come together to form small, irregular grains that can be as large as the Fullerenes. These grains play an important role in the conduction of the current away from the LCCs and onto the superconducting sheets.
The diamagnetic strings move somewhat randomly through the centers of many of the polygons in the sheet material. This motion mimics the motions of cations through protein membranes and groups of water molecules. In an F60 Fullerene, there are 20 hexagons and 12 pentagons. The pentagons do not have enough room in their centers for ions to pass through, but the hexagons do. The pentagons hold all of the Fullerene Crystals together. They provide positive geodesics with their curvatures, and only 12 of them are required to close the surface into a sphere.
The hexagons on the surface of a geodesic provide pathways for cations to move through, from inside to outside and from outside to inside. If all 20 hexagons hold a single diamagnetic atom, and there is one additional atom at the center of the geodesic, then there are a total of 81 for the entire structure (60+20+1 = 81).
Dopant atoms also bond into the negative sheets. The center holes in the hexagons are much larger in these than in the positive sheets because of the greater atomic radii, so only large cations can bond with these structures. Smaller ones will move through the holes without bonding. In these structures, the pentagons will hold the dopant atoms while the hexagons will allow them to pass through. These pentagons act as termination points for a single sheet of contiguous polygons, just as the pentagons anchor the side chains in cholesterol. These structures curve the ends of each over, limit its size, and define its dimensions within the larger crystalline complex of the LCC.
Each polygon sheet has dopant atoms, which are a mixture of magnetic, diamagnetic, and other cations attached to the inside portion of its curved surface. If two sheets come together, a rigid cage is formed around all of the dopants. This cage is the basic unit cell of these materials, as it is its smallest formation. Its size varies, but is in the range of 30 x 60 Angs. with a thickness of about four atoms (10-15 A).
When the craft is operating, the diamagnetic strings superconduct electrons out from the LCCs and onto the superconducting sheets. They provide the vital interface between the superconducting sheets and the metol side chains, and between the acoustical energy of the side chains and the electron energies of the sheets. In the LCCs, these atoms join with the magnetic vortexes to energize electrons that are used to produce luminescence in the LCCs and superconduction in the sheets.
The motion of electrons through the composite materials of the craft is complex. The initial current has a very high amperage and low voltage, but its energy is increased inside the spiral vortexes of every LCC through pinning.