There is no offset on the Beck, what is has is a low frequency so each transition is followed by either a positive or negative level of 125 mSec. The effect is that the bias during that 1/8 second is sufficient to cause the broken dna to move apart. If you run the frequency up then the dna segments will not have time to seperate sufficiently, and when the next half cycle comes, they will be brought back together. That is why the Clark Pulser must have a bias (unipolar pulses) so the pieces will be continually forced apart so they cannot rejoin. Same effect, same problem different solution.
Marshall Peter Rebaudo wrote: > Marshall, Friends > > My Beck Blood Elecrifier, fab. by Sota, has a Bi-Phasic square wave > output of 40V at 4 Hz.. > > My Hulda Zapper is 5V square wave @ 30K Hz with a 1/4 V positive offset. > > Can you please expand on your statement about the Beck's offset. > > Regards > > Peter R > > Both the Beck and Clark zappers work. They both work by the same means in > fact, but I prefer the Clark because it does not cause the > electrophoration, and I believe I somewhat more effective due to the > higher frequency. Here is how they both seem to work: > > 1. There is a fast transition of a pulse followed by a bias in the pulse. > > 2. The fast pulse contains a large number of frequencies (if you look at > the Fourier transform of the leading edge). > 3. Different DNA is resonant with different frequencies. > 4. The energy of each frequency is divided among all the DNA of that is > resonant with that frequency. > 5. There is so much of the body's DNA that the power for it's resonant > frequencies are essentially nil, thus the body's DNA does not break > apart. > 6. There is very little of the pathogen's DNA present, so each strand of > it's DNA receives significant power, sufficient to cause the DNA to > break part. > 7. When DNA breaks each end has an opposite charge, so normally the DNA > will immediately be attracted back together and rejoin with no harm > caused to the structure the DNA is part of. > 8. Both the zapper designs provide that a bias is present (the Clark an > average bias continuously, and the Beck on a bias for about 1/100 of a > second), which causes the broken oppositely charged ends to be > attracted > into opposite directions, so that they are unable to find each > other and > thus the break becomes permanent. > 9. The broken DNA kills the virus or cell that the DNA is part of, or at > least makes it so it cannot reproduce. > > The requirement for 1/100 second or more bias to be applied to separate > the ends is why the Clark Zapper MUST be unipolar pulses, and not > bipolar, and why when using bipolar pulses like the Beck design, the > pulses must be no more than about 100 Hz. > > Marshall > > -- > The Silver List is a moderated forum for discussing Colloidal Silver. > > Instructions for unsubscribing are posted at: http://silverlist.org > > To post, address your message to: [email protected] > > Address Off-Topic messages to: [email protected] > > The Silver List and Off Topic List archives are currently down... > > List maintainer: Mike Devour <[email protected]> >
