Mike, Everybody, Maybe I spoke too soon. For this batch I've used a tiny drop of honey as starter. Now after 3.5 hours the CS is as dark red as I've ever seen it, gray to reflected light. After the next time weighing the electrodes I'll let you know about ppm. Reid
Reid Harvey said: Mike M., Everybody, There seem to be a few unforseen glitches with production of concentrated CS, and I'm working to resolve these one by one. Now I'm hoping someone can cue me to what's necessary in the event of low current/ low conductivity, since I believe this to be the problem I'm facing, since I believe this is seriously cutting my ppm per time. Again, it's 30 volts DC with a 2.4 liter erlenmeyer flask, maintained in a double boiler at about 96C. I've accustomed myself to the uneven switch times for polarity reversals, periods differing per electrode. And now I've done weighing of electrodes before and after, so as to determine ppm, where this is not ionic. But over quite a long time I only got about 100ppm. I'm not certain low current due to low conductivity is the problem, but I do know that for these last two production runs it took me about double the time of previous runs, in which I had done manual switching. This time I added a drop of honey, to increase conductivity, which I believe should be okay where the output is not ionic. Would using a starting in this way be something that could be otherwise optimised. What material and how much?, given that I'm going very very high concentrations. Mike, you said something earlier about making a device constant current. How could we modify the diagram to get that? Thanks, Reid -- The silver-list is a moderated forum for discussion of colloidal silver. Instructions for unsubscribing may be found at: http://silverlist.org To post, address your message to: [email protected] Silver-list archive: http://escribe.com/health/thesilverlist/index.html List maintainer: Mike Devour <[email protected]>
