Originally Posted by
Jay DeFehr
When graded printing papers dominated darkroom shelves, photographers had to learn to scale their negatives to their printing papers, and to adjust print contrast for between-grades, by the manipulation of exposure and print developers. A practical knowledge of sensitometry and basic chemistry was indispensable to serious photographers, and a wide range of testing and calibration procedures evolved to aid the photographer and darkroom worker.
Hybrid film/digital workflows represent a similar shift in the demands on the processing film to be scanned for either digital printing, or making digital negatives for contact printing, and suggests new criteria for film developers.
A film developer for film to be scanned should be optimized for producing the kinds of negatives that scanners are optimized to scan, or in other words, for maximum compatibility.
What kind of negatives do scanners like best?
Grainless
low contrast/ low-moderate density range
high resolution
And, while scanners don't care, photographers almost always prefer high film speed, long shelf life, economy, ease of use, and low toxicity, all other things being equal.
While there are developers commercially available that possess some of the characteristics listed above, none are optimized for the entire description, and other desirable characteristics could be added, such as: long tray life, compatibility with rotary processing, commonly available ingredients, etc.
I think we have within our membership the experience and expertise to narrow the many options to a few, high probability approaches to distilling something like an optimized developer for film to be scanned. I have a few ideas of my own, and more questions. I hope there is enough interest to generate some positive discussion and debate on the most likely approaches. I'll try to start the ball rolling by suggesting Pat Gainer's PC TEA, which I think satisfies most of the criteria, with the exception of the "grainless" one. It might be possible to use some variation of PC TEA as a two- part developer by diluting the concentrate with a sulfite solution. An even less toxic version might use glycol in the concentrate, and add a less toxic alkali to the B solution. In any case, I favor a simple, ascorbate/ phenidone concentrate made up in TEA or glycol, but I welcome alternative opinions, and I hope for many.
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