Pulse Probing the Atomic Bi-IV

Crystal at Near Resonance

Pole zeros are caused by adding a
finite number of input samples
together and poles are caused by
feedback. Nuclear dipole resonance
is a feedback phenomenon, whereas
crystallographic ionic potential is a
feedforward phenomenon. (ref. pole
and zero filters used in the
tetrahedral design). This is the same
arrangement as a pair of inverted
triangles, each formed by joining
three ions on a side to a single ion at
its vertex.

If we require that the magnitude and

direction of the equal and opposite
crystallographic pole phasors and
zero phasors are attached pole/zero
pairs of orthogonal phase "flipper"
vertexes, we can assume a dipole
resonance exists between
diametrically opposed ions in the
"cube" diagram when a polarized
pulse sequence is applied to the BI-II
dipole.For example, we can pulse the
green orthogonal group of circularly
polarized phasors with their red
counterparts.

Likewise, the blue orthogonal group of circularly polarized

phasors can be pulsed with their magenta counterparts. Each
of these pulse pair sequences represents a dipole resonance
sequence. On the other hand, rather than representing
opposite faces of the cube, the pairs of phasors can be
resonated on one face of the cube, so that the direction of
atomic g-field decompression is in the direction perpendicular
to one of the 6 cube faces. This represents the gradient of
magnetic field decompression, or "g". For this example, the
gradient "g" represents the twin pair of resonating red and
magenta phasors. The conditions for formula (3) for the
values of a and b vary between being elliptically polarized
and circularly polarized, meaning that the amplitude values of
a and b are equal for circular polarization, along with having a
difference in phase angle always being π /2, but are different
for elliptical polarization, for differing amplitude between a
and b, as well as phase angle.

The phase angle for elliptical polarization differs by (n+1) increments of π /2, where n=1 or more. Note that only for elliptical
polarization, the values of n=1,3,5,... represent phasors that are 180o out of phase for dipole magnification, but the values of
n=2,4,6... represent harmonics of the n=0 condition for maximum decompression. At the n=0 condition for elliptical polarization,
the only difference between being circularly polarized is that the amplitudes of a and b are not equal, meaning that the resulting
gradient is not directly orthogonal to the face of the cube.

We can now imply a condition for the n's and φ 's in formula (3): Since the φ 's are always multiples of π /2 and equal for both a
and b in both elliptical and circular polarizations, the n's in the formula for an and bn can only equal 0,2,4,6,... for elliptical
polarization ( ), and 1,3,5,7... (a=b) for circular polarization. The pulse polarization sequencing controls the amount and
direction of gradient off each of the six faces of the cube.
Analysis of the Pulsed Cubical
Membrane
Within the crystallographic boundary for the diamond shaped lattice we can superimpose a cubical membrane that represents a
crossection of the decompressing "g" wave instantaneously over two of six faces of the atomic crystal. The geometry of this
configuration is assumed to incorporate a hyperbolic shockwave distortion off of opposite faces of the cube, similar to the sphere
inscribed over a square surface, whose radial component becomes either elliptically or circularly polarized to two of the six faces
of the cube. The instaneity of atomic field decompression is such that only opposite faces of the cube can be "decompressed" per
pulse interval. The maximum level of decompression depends upon the characteristic surface of the normal. We are going to
assume that this distortion is an average over the species (grey surface "neighbors") using a converged lattice potential sum
profile for ionic neighbors as a function of distance for the body-centered cubic structure.
Solution to the Cubicle Membrane
Problem

In order to obtain uniform convergence of the series for u and its first and second derivatives we must assume that f (continued as
an odd function) and its partial derivatives up to the third order are continuous, while the squares of its fourth partial derivatives
have finite integrals. Also g and its derivatives up to the second order must be continuous, and the squares of its third derivatives
must have finite integrals. While this condition is somewhat too strong, it is known that a discontinuity in the third derivative of f
can produce a discontinuity in the second derivative in u. Discontinuities are propogated along characteristic surfaces. These can
degenerate, producing a loss of derivatives (focussing).

By our uniqueness theorem u(x,y,z,t) depends only on the part of the data in and on the sphere of radius ct centered at (x,y,z).
However, this is not all clear from the form used above for the solution. This formula expresses the solution as a sum of simple
harmonic motions, in each of which u is a product of a sinusoidal function of t with a function of x,y, and z only. These motions are
called the normal modes of the problem. Their frequencies [sqrt (l2+m2+n2)c/2π ] are called the characteristic frequencies. Note
that the characteristic frequencies mentioned here are related to the vibrational frequencies of the Bi-II diatomic molecule at or
near a resonant condition. Let us examine the resonant condition more closely with the four-dimensional tesseract representing
the translation of a diamond body centered cubic in space and time.

If we know the natural frequency of the absorbing magneton, we can use the resonance phenomenon to determine the frequency
of the incoming signal. First of importance, then, is the close correspondence between the incoming signal frequency and the
natural frequency of the absorbing system. When resonance absorption occurs, energy is taken out of the incoming wave and is
absorbed by the resonating medium. Atoms and their nucleii are like swiftly rotating little gyroscopes. Instead of wiggling to and fro
like a compass needle in the earth's field, they precess around and around the direction of the applied field, just as a gyroscope
precesses around the earth's gravitational field. Each atom or nucleus will have a characteristic precession frequency, or a
wiggling frequency, in an externally applied magnetic field. The magnetic fields that are applied to a nucleus are determined not
just by the the average and uniform field strength between the poles of a positronium pulsed power supply, but also by the field of
electrons surrounding the nucleii. The energy required to 'turn around' the nuclear magnets of two Bismuth atoms (in a dipole
configuration) has been measured very precisely, i.e., the magnetic moment of bismuth is calculated using the magnetic mass
/
susceptibility for Bismuth χ p (10-8m3kg-1) = -1.70. The resulting magnetic moment in amps-meter2 is the amount of mass in
kilograms of bismuth times the susceptibility χ p, (using a field strength of 1 amp per meter).
In order to visualize the diamond body centered cubic translated into four dimensions, the cube would have to translate
perpendicular to all of its edges, forming a hypercube, or in this case, a tesseract, as shown here. In a tesseract, all six faces of
the cube have extensions that are similar to pyramids without their 'caps' on them. In a nuclear hypersphere, each individual
nucleus will have a different gravitation constant consistent with the “Binding Energy per Nucleon” for the outermost ground state
energy level nucleons, which is directly related to the intensity of the “Strong Nuclear Force” just outside the nucleus. Notice in the
graph at right that resonant frequencies of Magnetoreflection spectrum of Bi transitions shift with the magnetic field strength in
Teslas. The corresponding frequencies for the resonant shifts correspond to dramatic drops in the radiocity parameter (on the
vertical axis). The heavy electron band (Fermi level) resides around a magnetic field strength of 35 Tesla. This level represents
the highest radiosity shift available for an applied polarized positronium pulsed probe beam. The Fermi levels relate to the outer
shell spectral emissives, which become occupied based upon the distribution of energy levels and the number of electrons
available. We have indicated only one side of a tesseract in the above left diagram in order to better visualize the concept of a
swollen nucleus initiated by a pulse probe*. The cumulative effect of expanding valence fields for thousands of crystals
simultaneously means that there is a large negative nuclear pole decompression that acts directly opposite to the direction of the
applied probe beam.

*There are, of course, ideas related to the transfer of energy in the 'perfect' diamond body centered cubic related to thermal
gradient and lattice distortions, but we can assume that these are only side effects of the larger g-wave decompression that
expands the 7th shell valence field of the BI-II dipole.

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