Yup. D76 outperforms D23 and the ingredients cost less (becuase HQ is MUCH less expensive than Metol/Elon).
D76 makes D23 a historical curiosity.
Ilford's Perceptol a historical curiosity as well? From what I've seen of John Finch's videos on it it looks to do a very job of developing
the best thing you could do ... was to take a decent dose of .... red wine.
Doesn't that make Ilford's Perceptol a historical curiosity as well? From what I've seen of John Finch's videos on it it looks to do a very job of developing
pentaxuser
More importantly, packaged D-76 outperforms home-mixed D-76 (due to the latter's pH change over a period of a week).
WoahMore importantly, packaged D-76 outperforms home-mixed D-76 (due to the latter's pH change over a period of a week). Combine that with the discounts that come with buying chemicals by the train car load, and you find commercial D-76 costs hardly any more than home mixed, and it's more consistent and less prone to measurement errors and "Did I already mix in the metol?"
There is one significant advantage of D-23 over D-76: hydroquinone is a known or suspected carcinogen, and it's not present in D-23. Mind you, photographers don't have the kind of cancer rates organic chemists do, but it's there none the less.
Agreed. Especially if I mix the gallon size (10.42€ at fotoimpex) and my soft wine pouch is a good enough Oxygen barrier over the X months it takes me to use 1 gallon.Combine that with the discounts that come with buying chemicals by the train car load, and you find commercial D-76 costs hardly any more than home mixed
More importantly, packaged D-76 outperforms home-mixed D-76 (due to the latter's pH change over a period of a week).
Here's a quote from a posting in photo.net about the rise in activity of D-76:
In reading a paper by John Sexton about T-Max films he states "If you use D-76 developer be sure to use FRESH D-76 (not some that has been sitting around in a half full bottle for a month!) As D-76 ages, a chemical compound, hydroquinone monosulfonate, is formed. This chemical compound will INCREASE the activity of the developer and the contrast of your negatives in a big way with T-Max." I wonder if this is not the increased activity that is being attributed to a rise in pH?
He attributes the rise in activity to the formation of HQMS and not due to rising pH. Does anyone know whether this is true?
I've always wondered about this supposed rise in pH. D-76 is buffered by borax, so what could cause its pH to rise?
If this is real, how come the entity previously known as Eastman Kodak, that gave so detailed directions:or is this a "red herring"
Indeed. Old or well-used D-76 first goes through a phase of high pH and high activity, before dying completely. But that is quite different from the alleged initial rise in activity of freshly mixed D-76 over hours? days? weeks?Ok quick clarification; The D-76 used in my anecdote was Kodak packaged, not formula mixed. The 'well-aged' D-76 would be less than 1/3 full in plastic gallon jugs, and would be kept for 2-3 weeks after the week it was mixed.
That 'well-aged' juice would be used for pushing, however! J
Actually, both are correct. HQMS is actually a mild developing agent, much milder than hydroquinone. But it is produced by the reaction of p-benzoquinone in the solution with sodium sulfite, which is already present. P-benzoquinone isn't an ingredient of D76, but an oxidisation product of hydroquinone. When p-benzoquinone reacts with sulfite, HQMS is produced, but also sodium hydroxide. So yes, in a way HQMS synthesis makes D76 stronger, but it's the hydroxide that does the job. Now, if you use the D76d formula, which uses a borax - boric acid buffer, the effect might be smaller. To be honest, I've used old D76 many times and never really saw any difference, although I keep it in full, tightly capped bottles. And I've never mixed the original D76 formula. Ready made D76 is also supposedly better buffered.
Thanks for posting this explanation. As a check on my understanding, I'll summarize it in my words:
Hopefully I got that right.
- Oxygen oxidizes hydroquinone.
- Oxidized hydroquinone produces p-benzoquinone.
- P-benzoquinone reacts with sodium sulfite to produce HQMS and sodium hydroxide.
- Sodium hydroxide raises the pH.
This brings up another question: PQ developers contain hydroquinone, so why do we not hear about their pH rising? Are they buffered better?
I suggest that because there is usually only about 1/10 the quantity of phenidone compared to metol it may not react with air 10x as fast which would be needed to produce the same amount of benzoquinone and hydroxide from the hydroquinone so the pH would not rise to the same extent.This brings up another question: PQ developers contain hydroquinone, so why do we not hear about their pH rising? Are they buffered better?
I suggest that because there is usually only about 1/10 the quantity of phenidone compared to metol it may not react with air 10x as fast which would be needed to produce the same amount of benzoquinone and hydroxide from the hydroquinone so the pH would not rise to the same extent.
What does the quantity of metol or phenidone have to do with oxidation of the hydroquinone?
IMO, it's much more likely that PQ developers are just better buffered than (1930s vintage formula) D-76.
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