I present here an odorless quick acting fixer based on Sodium Thiosulfate:
200 g/l Sodium Thiosulfate Pentahydrate (= crystalline)Resulting pH is about 6.5, which makes it near odorless (neither sulfite nor ammonia odor), quick acting (not as fast as Ammonium Thiosulfate based fixers, but close) and quick to wash out.
40-45 g/l Ammonium Chloride
10 g/l Sodium Sulfite
2.2 g/l Sodium Metabisulfite
Since paper and film properties are all over the place, I can not provide...
Rudeofus submitted a new resource:
A Neutral Quick Fixer Formula - odorless neutral sodium thiosulfate ammonium chloride fixer formula
Read more about this resource...
Rudeofus submitted a new resource:
A Neutral Quick Fixer Formula - odorless neutral sodium thiosulfate ammonium chloride fixer formula
Read more about this resource...
There were several Sodium Thiosulfate plus Ammonium Chloride based fixer recipes out there, and I did inherit some of their concepts in my concoction. There is Agfa 304, which I initially used to fix my prints. At a later point I ran across OF-1 fixer, which is quite alkaline and therefore IMHO unsuitable for open tray processing. I did get a lot of advice from PE about quick fixers with long shelf life. Here is the rationale behind the fixer recipe as posted here: <snip>
In order to get the ingredients dissolved with the least amount of time, I recommend the following procedure:@Rudeofus thanks for the recipe!
When mixing it should I follow the order in the listing? I mean first dissolve hypo, then add Ammonium Chloride and so on
Thank you, much appreciated!In order to get the ingredients dissolved with the least amount of time, I recommend the following procedure:
- Fill a container with about 60% of intended fixer volume with hot tap water (50-60°C/120-140°F).
- Add the calculated amount of Sodium Thiosulfate
- Stir vigorously. The Sodium Thiosulfate will cool down the water substantially while it dissolves. If you do not start with very hot water, the solution will get close to freezing point and dissolution will be extremely slow.
- After the Sodium Thiosulfate has been dissolved, add the Ammonium Chloride. This will cool down the solution yet more. If the volume is still below the intended final volume, add hot water to reach it. Chances are, that the solution will reach roughly room temperature.
- Add the Sodium Sulfite and the Sodium Metabisulfate at once and dissolve it. You should now have an ever so slightly milky solution, which should be mostly odorless.
Or you could try your local agricultural supplies shop, as I did. I found 15, 5 and 1l bottles and got a 5l one for 15€.@Rudeofus: Thank you. I have since decades some 500g of Ammonium Chloride, bought to prepare T55 Selenium toner. Of course, I used only a small part; Now I can put it to good use.
It seems that Ammonium Thiosulfate is used as a fertilizer around here (EU). But it is sold by truckloads, or at least by the ton. I keep telling myself I should call nearby agricultural co-ops and ask if they would sell me 10 litres. Then I would have the ammonium, the thiosulfate, without the sodium.
I have made many experiments with Sodium Thiosulfate and Ammonium Chloride, and with my stash of Ammonium Chloride an amount of 40-50 g/l was the optimum value. Above 50 g/l fixing speed would actually go down again. I did see Relayer's postings back then and did notice the much higher level of Ammonium Chloride in his formula. TBH I have no explanation for this discrepancy, except for maybe significant impurities in my stash of Ammonium Chloride, which may not be present in Relayer's stash. My Ammonium Choride was technical purity at best, delivered in a crude paper bag holding 20kg. People with more refined products may be able to replicate Relayer's formula with better success, however, the beauty of my formula lies in the insanely cheap ingredients. By the time you have to use analytical grade components, you might as well use Ammonium Thiosulfate.Rapid fixer without Ammonium thiosulfate | Photrio.com Photography Forums
What do you think of the fixer investigated by Relayer, post 9, solution 2?
Sodium Thiosulfate.......................200g
Ammonium Chloride......................86g
Water to..........................................1L
Suppose it was kept in a sealed container to avoid oxidation and pH drop and used only for film?
<snip>
So, I proceeded further with my little concoction and gradually added sodium sulfite and measured the pH. The first gram shifted the pH to 7.9, but each subsequent gram shifted it only by 0.1 unit, so at 4 grams (that is 40 g/L) it was 8.3, practically the same as in a typical fine-grain developer. One could stop there, too, because there is only barely detectable smell of ammonia, but I changed the pH back to neutral (6.9) by addition of 6 ml of 15% sodium bisulfate (this is sulfate, not sulfite).<snip>
Question: is that expected to significantly decrease the odor?
I expect this to be a safe approximation, yes.Can I assume that the proper/safe fixing time for paper is in proportion to the clearing time, i.e. if the clip test clearing time for your fixer is 1.5x (say) that of commercial fixer "X", then the same extension factor can be applied to the times listed for paper fixation?
@Rudeofus and all,
I see two possible remedies:
Capacity. Clip tests with film (traditional grains) for both the paper and the film fixer; I already do them regularly; discard when clearing time is 2x initial value. Agree?
- Neutralize the Foma fixer with ammonia (pH paper or pH meter).
Question: is that expected to significantly decrease the odor? Would you generally recommend this approach? Pro: no need to procure/store thiosulfate, ammonium chloride, bisulfite, and mix them.- Use your formulation. Pro: properly tested as such versus tinkering with a commercial product. Then there are the following issues questions:
Neutralize the Foma fixer with ammonia (pH paper or pH meter).
Question: is that expected to significantly decrease the odor? Would you generally recommend this approach? Pro: no need to procure/store thiosulfate, ammonium chloride, bisulfite, and mix them.
A little lower AFAIK; 7-7.5 But that's not a very meaningful difference.Fixers for C-41 are specified having a pH 7.5...7.8
AFAIK the main reason for B&W fixers to be acidic is to prevent dichroic fog under conditions of developer carryover due to failure to use a stop bath or thorough rinse. Since in C41 processing, there's the (acidic) bleach between the dev and fixer, the fixer doesn't need to be acidic. There's to the best of my knowledge no disadvantage to having a pH neutral fixer; if anything, the opposite, as it should prolong the lifetime of the fixer concentrate. An acidic fixer is more prone to sulfuring out.What are the trade-offs?
How long will the stock fixer keep before it sulfurs out?
Is Champion still a reputable brand?
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