Re bagging combined dry mixtures at home, note some compounds can be combined while others should not. For example I wouldn't recommend bagging any developing agents with other compounds. You're probably best off storing dry chemicals separately at home. Packaging dry mixes can actually involve some nifty technology such as coatings to keep dry compounds separated and allow them to dissolve in the proper order.
Packaging dry mixes can actually involve some nifty technology such as coatings to keep dry compounds separated and allow them to dissolve in the proper order.
Yes and not recommended.I am mixing the Diafine home brew recipe that's been posted here several times:
Solution A
Sodium Sulfite, 35 grams - Hydroquinone, 6 grams
Phenidone, 0.2 grams - Sodium Bisulfite, 6 grams
Water to make, 1 liter
Solution B
Sodium Sulfite, 65 grams - Sodium Metaborate, 20 grams
Water to make, 1 liter
1) Do I need to add the ingredients in the order listed and stir to dissolve? Are there any tricks like with D-23 (e.g., add a pinch of sulfite before adding the metol)?
Or,
2) While measuring, can I go ahead and make several bags of the combined recipe, all ready to mix with water? The powder comes in one can so I'm hoping this is a viable option.
Thanks!
I have no phenidone left. I wonder how well it would work with metol.
With divided developers all bets are off when it comes to the "normal" comparative working characteristics of different developing agents. With metol you might get slightly less film speed, and less fog, but experimentation is necessary. With metol you could likely simplify the formula, or even exclude HQ.
Note the formula posted above is rather generic and will likely require optimization. For example, it doesn't contain a restrainer, which would normally be expected in a PQ formulation such as this.
Also note Diafine uses a carbonate alkali in bath B as opposed to a borate.
I'll be anxious to hear also. I mixed some when I couldn't get Diafine in time; I started a thread a while back. My test negs were very thin, but I was able to get what I needed by going through the process 2x before fixing - A/B, then a thorough rinse, then A/B again. I suspected my Phenidone, which is old and shows some discoloration, so the problem might not have been the formula. By the time I got a chance to compare with real Diafine, my home brew seemed to have gone off considerably more. Even Diafine doesn't seem to give much push to current TX, so I've moved on for now. It does give a nice low contrast negative with a lot of highlight compensation.
Humm, not my experience, unless Tri-X has changed again in the past couple of years. I get a good EI 1000-1200. I can use 1600 in daylight (say, heavy overcast) but more like 1000 in tungsten so I typically shoot it at 1250 or 1000.
Humm, not my experience, unless Tri-X has changed again in the past couple of years. I get a good EI 1000-1200. I can use 1600 in daylight (say, heavy overcast) but more like 1000 in tungsten so I typically shoot it at 1250 or 1000.
I'm curious how the home mix works too. Diafine is getting expensive, though it develops so much film it's still one of the cheapest developers per film. But it's long life and the fact it isn't as popular as more "normal" developers make me worry about it. I like my Diafine. I don't use it that much but when I want it, I want it (mainly for Tri-X at 1000 and for Pan F+.)
Roger,
How is the shadow detail on Tri-X at those ISO ratings?
Other people report similar results to yours. All I know is that I'm not getting the density I need at what I would call 1200 to 1600 EI. I do better with Acufine, but have moved to reduced time in Acufine followed by the Diafine B bath. That gets pretty much everything that is to be had in the shadows, but with good highlight compensation. This is mostly for one very dim venue and even that just barely gets me usable exposures. I've got a couple rolls from last weekend processed that way, but haven't had a chance to make any prints yet.
I don't think TX has changed. It is entirely possible that we are giving very different exposures.
I don't know who DF Cardwell is, but there are some problems with that reasoning.
First, bromides are one of the by-products of development. Since no meaningful degree of development occurs in bath A, and solvent effects are likely minimal, there shouldn't be bromide buildup. This is one reason why bath A can be re-used and doesn't require replenishment.
Second, Phenidones are not very sensitive to bromide restraint at the pH level of solution B.
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