Perhaps a good way to accomplish that would be to simply drain the cell
slowly out the bottom into a storage container with a petcock. When the
cell is empty, the CS is done and the drain rate determines PPM.
 Ken



At 05:18 PM 10/17/00 -0400, you wrote:
>Hey Bob.  You might give this a try.  Use constant voltage AND current with
>stirring.  Basically make it so the electrodes can be removed from the water
>incrementally, and slowly pull the electrodes out of the water as current
>tries to increase.  Once calibrated you could make CS of whatever ppm you
>want by marking on the container at what point the electrodes are at when
>you finish.
>
>Here is my thinking.  Increasing voltage, with all else unchanged, tends to
>reduce particle size because the higher gradient pulls the particles away
>from the anode more rapidly so the ppm does not build up as much near the
>anode.
>
>Higher current increases particle size, due to increase in particle density
>near the electrode.  That one reason that if you use constant voltage the
>particles tend to get large rather quickly once the current reaches a
>certain point.
>
>But if you use constant current, the voltage still drops off toward the
>end.  This I believe will increase particle size more than if the voltage
>could be maintained with the same current.  That can be accomplished by
>removing active area from the water.
>
>Now, it is true that the current density will go up as you extract the
>electrodes, which should make larger particles.  However the voltage
>distribution between the electrodes goes from being almost linear between
>the electrodes, to having the highest gradient near each electrode, because
>the electrode area has dropped, and the bulk conductivity of the CS has gone
>up.  I believe this increased gradient near the electrode will more than
>compensate for the higher current density.
>
>Anyway, you might want to give it a try.  I don't know about LVDC, but it
>seems to work that way with HVAC.
>
>Marshall
>
>
>
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