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sanking

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I started a thread a couple of days ago called “And yet another pyrocat”. The thread was started based on some preliminary testing I made in which ascorbic was substituted for one of the secondary reducers in the Pyrocat formula (for phenidone in Pyrocat-HD, for metol in Pyrocat-M or for p-aminophenol in Pyrocat-P).

After further testing, however, I concluded that the family of curves created by the pyrocatechin + ascorbic reducer was so significantly different from the family of curves of Pyrocat-HD, -M and –P, which are almost mirror images of each other, that the term Pyrocat-A would be inappropriate.

There were also other problems. Since pyrocatechin and ascorbic are not super additive, the function of the ascorbic is solely that of a reducer/restrainer. In other words, the pyrocatechin is doing all of the work, unlike the other pyrocat formulas where the secondary reducer constantly regenerates, so to speak, the pyrocatechin. So pyrocatechin + ascorbic works much like a straight pyrocatechin or hydroquinone developer, i.e. slow working at first, but after a certain amount of time they build contrast rapidly within a short period of time. If you were to test film at 4, 8, 10, 13 and 20 minutes you would find that about 80% of the contrast is built up in the period between 10-13 minutes, or at least that is the case when used in the Pyrocat formula. If you test Pyrocat-HD, -M or –P for the same amount of time, contrast is built at about the same rate for any specific duration of time between 4 and 20 minutes.

Another phenomenon I observed was that minor differences in type of agitation caused a very large difference in effective film speed. For example, in my initial tests I developed in a drum on a motor base running at about 75 RPM and film speed was comparable to what I get with Pyrocat-HD, -P and –M at the same time of development. However, when I tested with development in tubes in a water bath with very gentle agitation, say 5-10 RPM, there was a loss of more than three full stops of film speed. This happened with the 1:1:100 dilutions using ascorbic in amounts ranging from 0.05g/liter to 0.15 g/liter in the working. I mention this specific fact because much of the discussion in the other thread focused on the "optimum" amount of ascorbic.

So, for those persons who followed the other thread I just want to clarify that my reasons for abandoning this line of experimentation relate primarily to what I perceive as some major problem with the pyrocatechin + ascorbic combination, not to the personal issues which surfaced in the thread.

Further, my comments are meant to apply only to my own testing of ascorbic as a substitue for another reducer in the Pyrocat formula, not to any similar formulas by others.


Sandy
 
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Tom Hoskinson

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sanking said:
I started a thread a couple of days ago called “And yet another pyrocat”. The thread was started based on some preliminary testing I made in which ascorbic was substituted for one of the secondary reducers in the Pyrocat formula (for phenidone in Pyrocat-HD, for metol in Pyrocat-M or for p-aminophenol in Pyrocat-P).

After further testing, however, I concluded that the family of curves created by the pyrocatechin + ascorbic reducer was so significantly different from the family of curves of Pyrocat-HD, -M and –P, which are almost mirror images of each other, that the term Pyrocat-A would be inappropriate.

There were also other problems. Since pyrocatechin and ascorbic are not super additive, the function of the ascorbic is solely that of a reducer/restrainer. In other words, the pyrocatechin is doing all of the work, unlike the other pyrocat formulas where the secondary reducer constantly regenerates, so to speak, the pyrocatechin. So pyrocatechin + ascorbic works much like a straight pyrocatechin or hydroquinone developer, i.e. slow working at first, but after a certain amount of time they build contrast rapidly within a short period of time. If you were to test film at 4, 8, 10, 13 and 20 minutes you would find that about 80% of the contrast is built up in the period between 10-13 minutes. If you test Pyrocat-HD, -M or –P for the same amount of time, contrast is built at about the same rate for any specific duration of time between 4 and 20 minutes.

Another phenomenon I observed was that minor differences in type of agitation caused a very large difference in effective film speed. For example, in my initial tests I developed in a drum on a motor base running at about 75 RPM and film speed was comparable to what I get Pyrocat-HD, -P and –M. However, when I tested with development in tubes in a water bath with very gentle agitation, say 5-10 RPM, there was a loss of more than three full stops of film speed. This happened with the 1:1:100 dilutions using ascorbic in amounts ranging from 0.05g/liter to 0.15 g/liter in the working. I mention this specific fact because much of the discussion in the other thread focused on the "optimum" amount of ascorbic.

So, for those persons who followed the other thread I just want to clarify that my reasons for abandoning this line of experimentation relate primarily to what I perceive as some major problem with the pyrocatechin + ascorbic combinatoin, not to the personal issues which surfaced in the thread.

Further, my comments are meant to apply only to my own testing of ascorbic as a substitue for another reducer in the Pyrocat formula, not to any similar formulas by others.


Sandy

Thanks for clarifying this Sandy, and thanks again for all of the Developer and Developer/Film Research, Development and Testing you have done and shared with the community.

By the way, I recall that you posted (Azo Forum) some results and thoughts about your initial investigations into an ascorbic acid/Pyrocat combination back in December of 2004.
 
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sanking

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Tom Hoskinson said:
Thanks for clarifying this Sandy, and thanks again for all of the Developer and Developer/Film Research, Development and Testing you have done and shared with the community.

By the way, I recall that you posted (Azo Forum) some results and thoughts about your initial investigations into an ascorbic acid/Pyrocat combination back in December of 2004.

Tom,

First, thanks for your kind and generous comments.

Yes, I did experiment with ascorbic in the Pyrocat formula a couple of years ago, and the ascorbic made the developer much more energetic (fast acting), up to a point, and then the stain was killed. Pretty much the same thing happens with sulfite, though without quite as much extra activity.

What I did not realize at the time, though the information is right there in the literature as Ryuji has pointed out, is that pyrocatechin is not superadditive with ascorbic, so the extra energy I observed was obviously created by synergism with the phenidone in Pyrocat-HD.

I am pretty satisfied at this point with the three Pyrocats and am going to spend more time printing in the immediate future. Playing around with different formulas is interesting and I am by nature just curious to know what will happen if you do certain things, but I would like to think of myself first as a landscape photographer working primarily with LF and ULF equipment who makes hand-made prints with the carbon, kallitype and palladium processes, and on a secondary level as an experimenter with developers.

Sandy
 
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