Water Molecule Info

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    link: http://www.diamondhead.net/p10.htm

    Crystalline Water Dynamics in Biological Systems

    Water is a polar molecule;

    It has positive and negative charges separated by a dipole length

    and thus exists as an electric dipole.

    This is due to the 104.5o angle of the hydrogen bonds to the

    oxygen atom.

    The electro negativity of the oxygen atom attracts the electron

    of the hydrogen atom.

    Thus the region about the oxygen is negative compared to the

    region around the hydrogen atoms, which are comparativelypositive.

    Because of this molecular configuration, water molecules mutually

    attract one another due to the (-) and (+) regions.

    Individual water molecules are linked by these hydrogen bonds and

    form what are called clusters (structural water).

    In addition, water at an interface, as with the atmosphere, has a

    surface tension due to the polar interactions of water with other

    water molecules at the interface surface.

    Water has the capacity to align into 400-500 hydration layers

    (Gerald H. Pollack, 2001).

    At body temperature, there are about 300-400 water molecules

    cross-linked into a cluster.

    This clustering imparts a crystalline like property to the water.

    Water is known to crosslink in arrays from linear to helical.

    In the bodies of living organisms, the clusters form hydration

    layers around biological molecules.

    The entropy of "structural" water is not as great as that of solid

    water as ice, due to the greater content of thermal energy at body

    temperature. The water molecules of ice are aligned in a linear

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    array, with some branching, yielding a more rigid structure of

    expanded intermolecular domains than that of liquid water.

    For this reason, ice is less dense than water and as such floats.

    It is known from electronics that different patterns which contain

    information result within a cluster depending upon its structure.

    An example of this is gamma-iron that is used for the recording of

    information in digital form as discrete, local magnetic domains.

    Thus, depending on its structure, each molecule has an oscillatory

    pattern (resonance frequency) that can be determined by

    spectroscopy.

    It is known, through spectrographic analysis, that water and other

    dipole molecules are able to be entrained to exogenous oscillatory

    patterns by rearranging their cluster patterns.

    The cluster rearrangements then resonate with the entraining

    frequency.

    Quantum electrodynamics calls for the existence of long range

    electromagnetic fields that can be transmitted by large, hundredsof angstroms, coherent domains present in water (E. Del Giudice &

    E. Preparata, 1994).

    Electromagnetic field (EMF) interactions afforded by the capacity

    of water to support long range EMF fields yield the specific and

    rapid long distance attraction of co resonating mates.

    Coherent domains with laser-like properties have been described in

    water (E. del Giudice, G. Preparata, G. Vitiello, 1988).

    More recently, a unique type of stable (non-melting) ice crystal

    that maintains an electrical field has been identified and

    characterized in water.

    In the example of living organisms, it is the biological molecules

    of cellular architecture, membrane systems, cytoplasmic and

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    nucleoplasmic components and cellular organelles that entrain the

    water of hydration surrounding them.

    All biological interactions occur in water, since, on the average,

    there are ten thousand molecules of water per molecule of protein.

    These patterns persist through time, although not indefinitely

    without continued entrainment.

    This entrainment is able to be determined by various types of

    spectroscopy.

    These include quanta of electromagnetic waves (photons), quanta of

    the weak interactions (bosons) and of sound (phonons).

    Water molecules must line up in an electric field because of their

    bipolar nature.

    If the field direction is reversed, the molecules will about-face.

    As long as the frequency of the imposed field is not too high,

    water molecules will continue to flip with the imposed frequency.

    When the frequency is raised beyond a critical value, the water

    molecules will no longer be able to respond in timely fashion.

    For ordinary water, the critical frequency for this weakening is

    20 GHz.In structural water, the critical frequency drops to 10 KHz.

    Frequencies below these limits allow the structural water to move

    in resonance with the entraining frequency.

    Alternating current frequencies (50 Hz, 60 Hz) are well within

    this range and are known to deleteriously affect many biological

    processes (E. F. Block, 1994).

    The principle of Magnetic Resonance Imaging takes advantage of the

    orientation of the hydrogen nuclei of water (by absorbingexogenously applied electromagnetic energy) to orient in an

    exogenously applied stable magnetic field.

    Upon release from magnetic orientation, the hydrogen nuclei emit

    relaxation quanta as photons that are recorded and yield a picture

    of the "structural" water in the body.

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    Water is thus known to orient to the presence of magnetic fields

    as well as electric fields.

    This is particularly important when you understand that those

    persons with "healing" abilities are able to charge water by the

    application of emitted electromagnetic fields from their body,

    most usually the hands.

    Perhaps the earliest, most famous and controversial proponent of

    this phenomenon is Dr. Franz Anton Mesmer. Dr. Mesmer was able to

    charge the baquet with his "magnetic fluid" to the benefit of his

    patients.

    Modern researchers have studied many healers and the effects of

    their energy projections in water.

    Spectrographic analysis of the water before and after charging

    show shifts in resonant spectra and a decrease in surface tension

    (R. Gerber, 2001).