- Joined
- Jun 11, 2011
- Messages
- 19
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Ive been making the ostermans silver bromide gelatin formula for a year and im curious if it could ever get to iso 3 or 6 without sulphur or gold or by using ammonia. More for curiosities sake than any motive to avoid sulphur/gold. I'm interested in practicle simple steps rather than making it far more complex.
I *think* I've got it from iso .75 to iso 1.5 by a syringe pump set to a 20 min precipitation instead of the instructions which I think from memory are 3x 1 min precipitations of the silver with a 1 min holds. Everything done at 55deg with a 300rpm stirrer. then hold for 20 mins as per instructions.
I did recently try to rig something up with my syringe pump so that it pumpped air into a test tube of silver nitrate in a water bath which then made the heated silver nitrate siphon off up another tube into the gelatin at a nice constant 55deg c. Unfortunately the plates fogged very badly. I'm not sure if it was the precipitation itself or maybe the tubing used etc that caused the issues
I'm wondering if any neat tricks could be employed in the precipitation / holding or maybe even the spinning peanut could be hindering crystal formation.?
I have an old book on emulsion making that had a chart of grain size Vs precipitation speed and it seemed to be a fairly significant increase in crystal sizes with very slow precips I don't really see any formulas that employ a very slow precipitation. My own findings seem to show it maxes out at iso 1.5.
There's lots a talk about the post wash heating making a bigger speed increase but my slightly dubious testing has indicated a 44 min post wash cook made absolutely
no difference, I'm wondering if it's ineffective without sulphur/gold/active gelatin?
I *think* I've got it from iso .75 to iso 1.5 by a syringe pump set to a 20 min precipitation instead of the instructions which I think from memory are 3x 1 min precipitations of the silver with a 1 min holds. Everything done at 55deg with a 300rpm stirrer. then hold for 20 mins as per instructions.
I did recently try to rig something up with my syringe pump so that it pumpped air into a test tube of silver nitrate in a water bath which then made the heated silver nitrate siphon off up another tube into the gelatin at a nice constant 55deg c. Unfortunately the plates fogged very badly. I'm not sure if it was the precipitation itself or maybe the tubing used etc that caused the issues
I'm wondering if any neat tricks could be employed in the precipitation / holding or maybe even the spinning peanut could be hindering crystal formation.?
I have an old book on emulsion making that had a chart of grain size Vs precipitation speed and it seemed to be a fairly significant increase in crystal sizes with very slow precips I don't really see any formulas that employ a very slow precipitation. My own findings seem to show it maxes out at iso 1.5.
There's lots a talk about the post wash heating making a bigger speed increase but my slightly dubious testing has indicated a 44 min post wash cook made absolutely
no difference, I'm wondering if it's ineffective without sulphur/gold/active gelatin?

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