Fine crystals on palladium prints

OP
OP

mikepry

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Mar 16, 2003
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Green Cove, VA
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Mike,
I usually develop for 2 minutes. I found, by some reason I can't explain, that my prints cleared better going from 1min up to 2 min. on dev. time.
 
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Mike,

The reason they clear better is that the developer is also a clearing bath, and a hot clearing bath is better then a room temperature clearing bath.

I see this as another benefit of pulling the print out of the PO faster, though, because I don't want the PO fouled up with FO and pt/pd salts, so the quicker it comes out, the less the PO loads up with that stuff. It does mean a little more effort on the clearing bath end however, to ensure complete clearing.

Once the moon aligns properly, you'll be back to making great prints again.


---Michael
 

EricNeilsen

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Sandy, I haven't seen it written other than in my book, but I trust my eyes. A cloudy bath indicates the formation of a solid. With distilled/RO water I have not seen the cloudy effects. The cloudiness will appear with HCL clearing bath as well as plain tap water; this was very evident when prints were made in Taos from wells. Potassium Oxalate has been made in my darkroom and those that I work in for the past 25+ years with ONLY distilled or RO water.

Eric
 

sanking

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Eric,

Well, you have convinced me on this, and I plan to mix the PO solutions with distilled water from now on.

What about the other question. Do you use tap distilled water (or reverse osmosis) for mixing the clearing baths?

Sandy




 

EricNeilsen

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Sandy, Sorry, I was trying to get some digital work done an djust used APUG as a break. I also use the RO water for 95% of my clearing bath mixing. When I was on a well in Taos, every trip to the store included a hand full of distilled water. The RO system has been great in providing good clean water.

I had two additional thoughts on the cystals that Mike was having problems with on his prints. Was that from the "hard to mix" developer? Perhaps you just didn't have your chemistry balanced and the solution that you beleived to be PO was indeed too heavy in Oxalic Acid? I have noticed over time of using it, that it has a tough time staying in solution (rather low soluability perhaps), and with the heated solution you are able to get it into solution, but after developing it, the print cools enough to allow the recrystalization of Oxalic acid?

What if you soak it in some hot distilled water?

What paper did this happen with?
 
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