The very low pH might be bad for certain film emulsions but I'm still convinced it's the permanganate that is abrasive to the emulsion rather than the acid, since dichromate bleach uses similar acid concentration without extensive emulsion damage.
Sounds promising! What film did you test this with, I'm guessing Foma400?
The very low pH might be bad for certain film emulsions but I'm still convinced it's the permanganate that is abrasive to the emulsion rather than the acid, since dichromate bleach uses similar acid concentration without extensive emulsion damage.
Yea, I would be curious on the shelf life of this bleach and how many rolls you can use before it goes bad.
Any evidence on how long this bleach keeps after mixing? One tank, one day, a week, a month, or as long as it stays blue?
Yes! I bought some garden supply copper sulfate, exactly. Sulfuric acid is super hard to get here except as concentrated drain cleaner, but citric acid is no big deal at all. Since it's reasonable sized crystals it's way easier and safer to handle.Nice! I can get copper sulfate pure enough for our purposes at the Big Box home improvement stores (sold for clearing roots out of drains). I actually have sulfuric acid on hand (30% strength, for battery filling), but I think I have some citric acid, too, and I'd worry less about handling that. ORWO DN21 has a very clear base, I may have to give a try to reversing a test roll.
Thanks Donald, that’s a great summarization!No one (that I know of) has reported film damage from unbuffered citric acid stop bath. Its solution pH is variously reported as low as 2 or as high as about 3.2. Sulfuric acid goes from about 2 if very weak to around 1.2 for solutions of the strength we'd use in copper sulfate or potassium dichromate bleach.
The difference between dichromate, copper sulfate, and permanganate bleaches relative to emulsion is their relationship with proteins. Dichromate has a tanning action -- it crosslinks the proteins in gelatin, hardening the emulsion. Permanganate has the opposite effect, breaking down proteins into smaller chains and softening gelatin. Copper sulfate is closer to dichromate in this regard. Further, permanganate is a very strong oxidizer (potassium permanganate crystals react with fatty substances -- notably glycerin -- rapidly enough to result in combustion).
Thanks! Hoping to get some decent shots from this. I tested with a couple of bits of film leader I had clipped from recent rolls. I believe it was Ilford Delta 100 and Agfapan APX-100 (Leverkusen). Ever since I did all that bleach testing at the end of the year I've been saving all the blackened bits of film from development efforts! Saves a lot of time vs having to get dark leaders when testing.
I bought some Foma first developer from Fotoimpex so I will try that and this bleach with some film this weekend when I get a chance.
This is what I was nervous about. If it's only 3 minutes, then it might be just fine. I certainly didn't see anything on the little bits I tested with.
You’ll prob have to adjust bleaching time for each films, but curious on your results!
@Raghu Kuvempunagar how long does the copper sulfate bleach normally take for you? I know you have used it a lot.
While Citric Acid alone is certainly very conductive to mold growth, the copper ions will stop any mold in its tracks. The only long time shelf life risk I see to this bleach is, that copper may - over time - oxidize the Citric Acid.Citric acid is an interesting substitute for sulphuric acid if it works. It might cause mould formation as it does in copper toner. So I would not be too optimistic about long shelf life.
While Citric Acid alone is certainly very conductive to mold growth, the copper ions will stop any mold in its tracks. The only long time shelf life risk I see to this bleach is, that copper may - over time - oxidize the Citric Acid.
Most likely, you can just bleach for longer than the slowest bleaching film needs. Generally, you'll take this process to completion (that is, you want to convert all image silver from the first developer to silver chloride so you can dissolve that with the ammonia), and I haven't heard any reports of copper sulfate damaging emulsion, so it ought to be safe to set a time long enough to always get the job done and leave it at that. I'd be surprised if it takes longer than four minutes for any modern silver image film -- which means, even including washes between baths you're only about doubling the time for regular development to get positives. You can do the bleach and ammonia in the light, so you shouldn't need a separate reversal exposure, just wash out the ammonia and go straight to second developer.
Some modern film emulsions are very thick and you’ll be surprised the time it takes to fully bleach one.
I used potassium hydrogen sulphate in place of sulphuric acid using the substitution formula given by Gerry Koch. I never used citric acid. Except for Adox CMS 20 ii which required about 5 minutes, bleach timing was at least fifteen minutes with some films like Carestream Ektascan xray film requiring even longer time. The bleach had a shelf life of at least six months and a capacity of at least ten rolls per litre.
While Citric Acid alone is certainly very conductive to mold growth, the copper ions will stop any mold in its tracks. The only long time shelf life risk I see to this bleach is, that copper may - over time - oxidize the Citric Acid.
Any modern C41 film developed in B&W reversal first developer takes a good amount of time to bleach. BTW Fuji Superia films make very nice monochrome slides when reversal processed albeit with a slight yellow tint.
My theory was also that once some silver is dissolved in there that will kill any mold as well. I know your fixer recipe works like that. I've had that fixer for months and it has been fine.
I've always been pleased with the results I got from copper sulphate bleach on a variety of films. It's not as convenient as dichromate bleach and the smell of ammonia is not nice, but it does give good results.Pretty happy with the result.
Sorry, you're mistaken. Copper sulphate bleach is a rehalogenating bleach; it doesn't dissolve silver. Rather it converts silver to silver chloride which remains on the film and needs to be cleared in a subsequent step using 2% ammonia.
Y
"Remember that any bleach containing Ammonium ion or Chloride ion is also, to some extent, a blix. This will cause loss of AgX in the remaining positive image in reversal B&W."
If there were indeed loss of AgX in the positive halide image due to the use of copper sulphate bleach, then it would have severely affected the shadows causing substantial loss of shadow detail. This is not what I noticed but something you can independently verify. I really doubt any noteworthy halide depletion happens because of the copper sulphatE
we don't really need to argue the point given that I am not sure any of us knows for sure. We'll see how the bleach lasts from testing.
I'd like to try this with paper negatives.
still worry about disposal or storage of the ammonia w/ AgCl. Maybe I am too cautious.
I have never had Copper Toner working solution last more than a few hours, therefore I would not expect to observe mold growth in working solution. Which recipe did you use?I never used citric acid in copper sulphate bleach but I've observed mould formation in copper toner. Maybe it is due to the warmer temperatures in this side of the world.
These 8.5% Ammonium Chloride, were these indeed 85 g/l ?
With Ammonia, you have an ingredient, which just complexes silver ions to form a soluble compound. With chloride and silver, you create a balance between insoluble Silver Chloride and soluble silver chloride complexes of the [AgCln+1]n- form. With little chloride in the mix, the balance will tilt towards insoluble Silver Chloride, that's, why Sodium Chloride works as restrainer in RA-4 color developer. With lots of chloride in the mix, you get silver solvent behavior, c.f. Microdol.
I would therefore suspect, that much higher concentrations of NH4Cl would give much better solvent behavior. If you have a cheap source of Ammonium Chloride and are willing to experiment, then I'd suggest 200 g/l or more Ammonium Chloride as a next test.
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