Hydroquinone Clearing Agent. How about THCA? Bill
mentioned the subject years ago on rec.photo.darkroom
and still no THCA.
Hydroquinone can be washed out at about the same rate as thiosulfate from non-hardening fixer.
This is an excerpt for your own reference. This is cut and paste from OCR of the paper so please pardon some conversion errors.
PHOTOGRAPHIC SCIENCE AND ENGINEERING. Volume 19. Number 2, March/April 1975 ¡"
Some Aspects of Fixation and Washing
A. Green
Research Division. Kodak Limited. Headstone Drive. Harrow. Middlesex, HA 1 4TY. England
ABSTRACT
The course of fixation and washing of silver-halide-gelatin emul·
sions is discussed with special reference to the swelling curves dur-
ing fixation and the emulsion conductivity during washing.
[...]
Monobath Processing-A Special Case
Washing after monobath processing differs from normal
cases because the monobath leaves the emulsion alkaline,
and contains developing agents as well as the usual thiosul-
fates. Hardeners are commonly absent and therefore the
washing out of the thiosulfate is very rapid because very
little is adsorbed to the gelatin. The main problem is the
presence of developing agents, largely hydroquinone, in the
alkaline layer.
We have investigated washing after a particular mono-
bath process in some detail, and a brief look at the results
points to general trends and slightly different requirements for archival permanence.
The "Dentech" process!8 is typical of modern monobath
processes in which a minimum of solution is used to process
each piece of film and is then discarded. In this case a small
water-tight packet containing the film is injected with mo-
no bath solution in the processing machine. The film is pro-
cessed in the machine's agitator, inside the packet, and
then finally is removed from the packet and washed in run-
ning water. It has been shown!9 that in this case, while a
40-sec wash in cold tap water is sufficient to lower the
thiosulfate concentration to the archival requirement, 60
sec is required to dilute the hydroquinone to a level where
it does not give a residual stain (see Fig. 16). These results
would indicate that as processing systems become more
rapid, some consideration should be given to the residual
level of developing agents if, even when the emulsion is fi-
nally at a lower pH, stain is not to be a problem after pro-
longed keeping.
The Figure 16 (not included) shows that hydroquinone level goes down with about the same time constant as the thiosulfate. Due to the difference in the initial concentration and stain-free level criterion Green used, hydroquinone took a bit longer to wash out in this case, using monobath developer and cold 12C washing water.
In conventional (non-monobath) processing, much of hydroquinone gets washed out in the stop bath, fixer bath and so forth, so hydroquinone gets washed out to the same criterion level much faster than Green showed.
"Just as a caution, one popular fixer out there is so poor that,
it spoiled on my shelf before I could get to test it, so beware..."
Likely one of those "rapid" ammonium fixers. I've got some of
that to dump as well. What remains of my bottle of anhydrous
sodium is in fine condition several years after being brought into
stock. If one is an off, off, and on such as myself at work in the
darkroom, a dry easy to mix concentrate is the ticket. Spoon
up fresh fix each turn in the lab. Dan
Most acid fixers, rapid or not, suffer from poor shelf life, especially once exposed to air or bottled in air-permeable containers. This problem is well known since 1960. Since I have the database at hand, I'll give you the abstracts of relevant research. Again, these are OCR'ed text and I haven't hand corrected them.
PHOTOGRAPHIC SCIENCE AND ENGINEERING
Volume 4, Number 2, March·April 1960
The Stability of Concentrated Ammonium Thiosulfate Solutions at High Temperature
G. 1. P. LEVENSON, Research Laboratories, Kodak Ltd., Harrow, England
Sodium and ammonium thiosulfate liquors were stored in sealed glass tubes at 60°C. The effect
of pH value, sulflte concentration, dilution, etc., on the time required ro bring about deposition of
sulfur from the solution was observed. The stability was not primarily dependent on whether so.
dium or ammonium salts were used. The stability rapidly decreased as the pH value and sulflte
concentration were lowered. Sulflte reacted with the thiosulfate and when oll the sulfite was
consume~ the thiosulfate decomposed.
The Stability of Concentrated Thiosulphate Solutions at High Temperature. Part II. The Loss of the Sulphite
G. I. P. LEVENSON (Fellow) and M. G. RUMENS
Research Laboratories, Kodak Limited, Wealdstone, Harrow, Middlesex
ABSTRACT. The decomposition of concentrated thiosulphate fixers at elevated temperatures occurs because
the sulphite is converted into sulphate and thiosulphate in a reaction catalyzed by the thiosulphate. When
the sulphate is gone the thiosulphate decomposes giving sulphur and sulphurous acid which latter is also lost
by the above mechanism.