Originally Posted by
koraks
I have some issues with this hypothesis, however. The metabisulfite is IIRC marked as optional in the glycol version, because it should not be necessary in a non-aqueous solution. So the question remains why the developing agent(s) would degrade in this solution that is very low in oxygen throughout its lifetime to begin with. The second issue I have with this hypothesis is that there is apparently no color change, which does not correspond to the mechanism of an oxidized developer. That is to say, it is conceivable that only the phenidone part has oxidized and that its color change is masked by the initial color of the part A concentrate, which tends in my experience to be light red to orange in a home-made glycol part A. In that case, I wonder if using dimezone-S instead of phenidone would be a good idea - which I cannot test, as I only have phenidone.
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