A couple of comments Trem, in your text. James Osbourne Holmes a...@trail.com
-----Original Message----- From: Trem Williams [SMTP:t...@silvergen.com] Sent: Friday, November 12, 1999 10:20 AM To: silver-list@eskimo.com Subject: Re: CS>Spectrophotometer, atomic absorption and colorimeter testing for PPM Hi Mike, Here's something else to throw us off. I just had several samples measured for PPM by a lab using the atomic absorption process. I asked them if they digested the CS before running the test. Answer was "yes". I asked them to run the test on each sample two times; once with and once without digestion. I did this because another lab had done the same tests for me without using digestion. I was interested in seeing what differences would be uncovered. Well, the results were strikingly different. With digestion (and by that I mean boiling in aqua regia) the PPM in 16 ounces of water using constant current production was about 3.5 PPM per hour. The highest reading sample was 35 PPM after running the generator for 10 hours and the reading for 5 hours was 18 PPM. Pretty straightforward I thought but then the undigested samples threw me off. They were 19 PPM for the 10 hour run and 11 PPM for the 5 hour run. These readings were still proportionate to time but only about 54-58% of the digested readings. The chemist told me that you cannot get accurate readings without complete digestion. I wonder how many of those using spectrophotometers, such as "Ole Bob" digest their samples. He told me once that he bleached the samples but didn't mention digestion. : Bob is just bleaching the "blank" used to calibrate the meter to 100% transmission. Since I really don't know that much about the process, I can't speak with much authority but I suspect that those using spectrophotometers would also get much different readings between digesting and not digesting their samples. I'd be interested in hearing reports from those who have them if they could run the tests both ways. JOH: Bruce Marx actually had a Hach guy in his lab. They finally determined that test to be reliable without the heavy duty hot acid and unreliable with it. If you send me a sample tested both ways, I will test it ---in confidence to you only---with the Hach set without digestion, for comparison. As a side note, I tried a Hanna instrument silver colorimeter and was disappointed. One used 4 different chemicals to react with the sample and the blank and then measured the color difference. When I ran the unit to test undigested CS, the reading was always zero PPM. In order to see if the unit was operable, I dissolved 1 mg silver in nitric acid by boiling and then added it to enough distilled water to get a 1 PPM standard solution. When I tested this sample, the unit did give a reading but it was very low (about 30% of the actual PPM). I sent the unit back because it was not working accurately enough with my home made standard and didn't work at all with the undigested CS. JOH: When you have only one clock you think you know the time. Afterward, I was told by the lab that did my last tests that digestion in nitric is not good enough. One should use aqua regia for complete digestion. So the upshot of all this to me was that you have to digest completely to get an accurate reading of the total amount of silver in the dispersion. It is possible I could have gotten better results from the Hanna unit if I had used aqua regia but I didn't know it at the time. There is so much controversy about this I am beginning to think there's some voodoo involved in getting accuracy. JOH: See http://borderlands.com/journal/lunar.htm Thanks for all of your work and sharing the data. Back to youse guys. Trem t...@silvergen.com ----- Original Message ----- From: M. G. Devour <mdev...@mail.id.net> To: <silver-list@eskimo.com> Sent: Friday, November 12, 1999 3:33 AM Subject: RE: CS>wet chem > > why not shop the net for a used > > spectrophotometer? I have seen several which will do the trick for > > about 400. You can get excellent really high-end but obsolete stuff > > for a bit more. > > Just curious: what kind of capability does this kind of spec have? > What range of wavelengths, UV, visible? Is wavelength fixed, manually > selected, scanned? Computer interface? > > What other parameters are important in evaluating the quality of such > an instrument? Sensitivity? Resolution? > > If I understand correctly, you use the hach reagents to digest and > mark the silver, then read the absorption on the spec. This is at a > fixed set of wavelengths, one wavelength, ... or what? Essentially > colorimitry? > > I'm looking for an overview, just so I understand how the pieces fit > a little better. If an investment of a grand would give me the > ability to do what I want to do, it'd be just worth thinking about. > > > I have just begun recording mS of my batches to plot against > > analyzed mg/L, more out of curiosity than anything else. Bruce Marx > > told me a couple of years ago that he had very poor correlation. > > Yeah, who knows with the hvac product? You could have such dependency > on water quality or other seemingly minor variables that it might not > work *because of the nature of the product*. But for a narrow range > of process conditions, Ivan is showing us a decent correlation > between ppm and conductivity in at least his lvdc process. . > > > And, knowing PPM, even with precision, is not very helpful in terms > > of effectiveness it you don't know anything about particle size. > > Which is one thing Marshall, I think, told us: there is a correlation > between absorption vs. wavelength vs. particle size. Which is why it > would be useful to have a scanning, or scannable, spectrophotometer > sensitive enough to directly detect the absoption characteristics of > samples of CS. > > > We are also into the realm of how many Angels can dance on the head > > of a pin: how many silver bits does it take to destroy [Can't kill > > 'em; my microbiology text says they aren't alive] one herpes > > simplex viron? Will a huge clump with a big charge do it, or is a > > single atom best? > > Well, if we can at least know the physical characteristics of what > we're making, we can then attempt to evaluate performance on the > basis of effectiveness, absorption, excretion, etc. > > One step at a time. > > Be well, > > Mike D. > > [Mike Devour, Citizen, Patriot, Libertarian] > [mdev...@mail.id.net ] > [Speaking only for myself... ] > > > -- > 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: > silver-list-requ...@eskimo.com -or- silver-digest-requ...@eskimo.com > with the word subscribe or unsubscribe in the SUBJECT line. > > To post, address your message to: silver-list@eskimo.com > > List maintainer: Mike Devour <mdev...@id.net> > > >