In a message dated 9/11/00 11:48:15 PM EST, [email protected] writes:
<< Subj: Re: CS>Why "spluttering? Date: 9/11/00 11:48:15 PM EST From: [email protected] (Del Crow) Reply-to: [email protected] To: [email protected] Ok... but some questions. What testing indicates bacterial and viral killing capacity at 1 ppm? Del: You are going to have to accept an "evidence" based perspective; we are not conducting double blind, clinical trials with hundreds of participants. Check the archives under my name around late spring early summer. At that time I came down with a terrible chest cold and my 1 PPM HVAC CS cleaned out the infection within hours AS LONG AS I GOT IT TO THE INFECTION SITE (ears, throat and lungs). Swallowing pints of (LVDC) CS appeared to do no good until I sprayed my HVAC CS down my throat (yes, I'm sure the LVDC CS would have worked as well). When a head cold flared up a day later, I sprayed it into my nose (lying upside down to get it into my sinus cavity) to relieve the sinus infection. This took a little longer to work completely (24-36 hours) probably because I had trouble getting it into the sinus cavity -- burned like hell. Doubtless some of the little stinkers would be effectively inactivated or killed...which ones have you tried your colloid on?. Is your calculation of the ppm unquestionably correct? Del: I don't know, but why should it matter? Years of experience with CS made by all imaginable electrolytic techniques (some good, some not so good) has demonstrated, again and again, that if you can get the CS to the site of the infection, it will work its magic within minutes, or even seconds. As far as knowing that I was indeed using 1 PPM CS, I have all my HVAC CS batches analyzed by AA from a lab that has demonstrated over the years to be quite reliable. I believe I could create a water-submerged arc, but a lot of control would be necessary. What difference "Pulsed" DC would make over AC, which is already pulsed would be another query I would have. Del: I must confess that I'm not very knowledgeable in the workings of HV DC or AC power Anyhow, since I have only roughly copied the CSPro web pictures of a couple of years ago, got my oil-furnace starter about a year ago, and use the CSPro printouts as guidelines as to what I am probably producing, I have to respect your calculations; mine are only guesses. During the last week or so, I decided to try our well-water instead of the RO water. I am not sure, in these few gallons whether the other minerals interfere a lot or very little. There is about the same 'low-level' Tyndall effect at four hours 10,000vAC as I used to get in those accidental 6 and 7 hour batches of RO I occasionally forgot about. Like some other people, I think that if you can see the light beam too many of the particles will not get much further than the bloodstream. Another thing, why would nitrates etc be produced anywhere except at the water-surface? I'm not ignoring that air is three-forths nitrogen. Did you test for nitrogen-related products where both AC silver electrodes were submerged in water about 2 to3 inches apart and the water was uncapped, or loosly capped? Del: No, but I never liked the CS product made that way. As I recall, it wasn't very stabile. To keep things as simple as possible, why not work with distilled water so product results will be easier to interpret. Roger -- The silver-list is a moderated forum for discussion of colloidal silver. To join or quit silver-list or silver-digest send an e-mail message to: [email protected] -or- [email protected] with the word subscribe or unsubscribe in the SUBJECT line. To post, address your message to: [email protected] Silver-list archive: http://escribe.com/health/thesilverlist/index.html List maintainer: Mike Devour <[email protected]>
