Over time, I've accumulated the leftovers of 5 five Tetenal E6 kits (3-bath process) - all 2/3 to 3/4 used. The oldest is from 2007, the newest from 2014. The chemicals all look alike: 1st developer with big chunks (sort of crystals), Blix part 2 with all the sulfur in small flakes settled on the bottom. The other solutions look just normal.
Now (1) I have a few slide films to develop, (2) no way to get a fresh kit before autumn, or none at all this year, (3) i'd like to revive the old stuff for economic reasons.
I'd like to learn your opinions (before actually trying out with real slide film) on the following approach:
1. 1st Developer: Filter out all crystals, mix 1:1 with Tetenal Utrafin T-plus, dilute 1+4 (or 1+3) with water, development time slightly extended - ~7 min, standard in my system would be 6:30 min. (Justification: Somewhere I read that Ultrafin+ was used to boost old E6 1st developer at 38°C. I also have Amaloco AM 74 / Rollei RHS - another PQ developer even faster on p.e. T-Max. Though no references for its use as a high temp developer.)
2. Blix: Option a) Carefully filter off all sulfur flakes from Blix part 2. Then mix the Blix parts 1 and 2 as required by instructions and use accordingly, however, after a wash, add another full fix with neutral rapid fixer at 38°C (standard dilution 1+7, e.g. Agfa Agefix).
Blix, option b) Rufeus wrote great instructions on how to split a blix into bleach and fix (Thank you and cheers!). Following this, dilute Blix part 1 (1+4) and add K-Bromide (>50g/l), adjust pH with conc. vinegar (acetic acid), and use this bleach in place of the blix (= Blix part 2 is omitted/discarded); after a wash, fix with neutral rapid fixer at 38°C (standard dilution 1+7, e.g. Agfa Agefix).
3. The other solutions will be used normally (diluted 1+4, times as per Tetenal instructions).
I normally develop films in a Photo-Therm rotary processor, which serves me well. Minimum volume, however, is 380 ml of solution (for 2 135-films).
I intend to do these development tests first on small pieces of film (~1.5 frames) in a small steel can (without reel). Would results be sufficiently indicative to be transferred to the rotary tube process?
I'd really appreciate your comments and notably experiences on the same or similar topic!
Best! Pitt
Now (1) I have a few slide films to develop, (2) no way to get a fresh kit before autumn, or none at all this year, (3) i'd like to revive the old stuff for economic reasons.
I'd like to learn your opinions (before actually trying out with real slide film) on the following approach:
1. 1st Developer: Filter out all crystals, mix 1:1 with Tetenal Utrafin T-plus, dilute 1+4 (or 1+3) with water, development time slightly extended - ~7 min, standard in my system would be 6:30 min. (Justification: Somewhere I read that Ultrafin+ was used to boost old E6 1st developer at 38°C. I also have Amaloco AM 74 / Rollei RHS - another PQ developer even faster on p.e. T-Max. Though no references for its use as a high temp developer.)
2. Blix: Option a) Carefully filter off all sulfur flakes from Blix part 2. Then mix the Blix parts 1 and 2 as required by instructions and use accordingly, however, after a wash, add another full fix with neutral rapid fixer at 38°C (standard dilution 1+7, e.g. Agfa Agefix).
Blix, option b) Rufeus wrote great instructions on how to split a blix into bleach and fix (Thank you and cheers!). Following this, dilute Blix part 1 (1+4) and add K-Bromide (>50g/l), adjust pH with conc. vinegar (acetic acid), and use this bleach in place of the blix (= Blix part 2 is omitted/discarded); after a wash, fix with neutral rapid fixer at 38°C (standard dilution 1+7, e.g. Agfa Agefix).
3. The other solutions will be used normally (diluted 1+4, times as per Tetenal instructions).
I normally develop films in a Photo-Therm rotary processor, which serves me well. Minimum volume, however, is 380 ml of solution (for 2 135-films).
I intend to do these development tests first on small pieces of film (~1.5 frames) in a small steel can (without reel). Would results be sufficiently indicative to be transferred to the rotary tube process?
I'd really appreciate your comments and notably experiences on the same or similar topic!
Best! Pitt