###  Ah, that clears up a lot of questions and makes sense.  There was a
fellow from a water softener company that came by here to test my well
water. He used a process similar to what you describe and compared the
results to a set of color charts.
[I guess I don't need mineral supplements :-)]
 KD'C


At 12:51 PM 4/6/00 -0600, you wrote:
>Re: Measuring the color and absorbency of sols.
>"If the particle size is so small as to not transmit a color, how would a 
>colorimeter possibly be used to accurately determine concentration?  There 
>is a direct contradiction here."
>You react the Ag with substance(s) which create another compound in direct 
>proportion to the available silver, and then measure with a photodetector 
>how much light gets through.  It is usually expressed in "absorbance", or 
>how much light did not get through the sample.
>One is the inverse of the other, but there is a math consideration which 
>makes absorbance easier to work with.
>The color solution---in my case, a clear magenta/purple---can be eyeballed 
> after some experience within a few PPM-mg/l after the color forms as the 
>silver is added to the prepared reagents.
>In the pre-electronic age it was done by visually comparing the strength of 
>the color sample of the unknown with a stable prepared set of solutions in 
>sealed tubes representing various concentrations.
>The instrument is zeroed to 100% transmission using a bleached [sodium 
>thiosulfate, same a photo bleach] sample of the reacted silver which is a 
>clear medium yellow, and the readout is set to Zero.  Then a test tube or 
>cuvette of the colored sample replaces the "blank" and the amount of light 
>absorbed is read.
>The measurement is made with light of a specific frequency [expressed in nM 
>of wavelength; i.e. color]  so that you are only measuring that light 
>absorbed by the reaction product.
>I know that I am calibrated correctly for Silver Nitrate [strongly ionized 
>monatomic Ag]  because I can take a sample of ACS grade silver nitrate 
>which has been diluted precisely with class A volumetric flasks and 
>precision pipettes to 4.0 mg/l and the Spec reads 4.0.  That is how I 
>created the slope on the graph with Absorbance up the X and concentration 
>on the Y axis, by measuring the absorbance of  6 different precise 
>dilutions .   This forms a "curve" which is really a straight line [the 
>process I am using is basically linear].  I used Excell [any spreadsheet, 
>graphing program will probably have the same function available] to do a 
>linear regression on the string of points to make a best-fit straight line 
>for the graph.
>Bob Berger gave me a great tip.  Lacking a program to construct the line, 
> view the dots representing the individual measurements at a very low 
>angle, [as in placing your head very near the surface on which the paper is 
>laying.   Your eye will 'see' the line through to dots well enough to do a 
>satisfactory linear regression by eyeball and brain.  You then draw it in.
>At issue is the reactivity of the metal particles with the color-forming 
>reagents.
>I do not know the precision available compared with AA spectroscopy, but it 
>is certainly good enough with wet chemistry to determine the Ag sol 
>concentration to at least a tenth of a mg/L.   With more sophisticated 
>instruments you can move the precision over to the right, but I am not sure 
>how far; I don't need it and could not afford it if  I did.
>The present issue for me is:  Will the reagents I am using react fully with 
>the metallic particles, or, as some say, it must be reduced to ionized, 
>i.e. individual "dissolved" atoms of silver. Some say firmly one and others 
>firmly the other.
>Other devices measure the amount of  and wavelength  of light refracted, 
>reflected, and absorbed with sensors at various angles to the incident 
>beam.  They then use a complex software algorithm to calculate particle 
>size.
>Any input based on experience or a reference regarding digestion v no 
>digestion  will be welcome.
>James Osbourne Holmes
>[email protected]
>



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