Photo Forum / Film Photography / Darkroom / May 2005
Do You Control the Print Development Temperature?
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narke - 02 May 2005 03:56 GMT while i can use water bath to get 68F for film development, however, i found the same method is hard to apply to print development for the tray is more large and flat comparing to a tank. my question is,
is there a recommended temperature for print development? and how should i get the temperature?
thanks in advance.
- narke
UC - 02 May 2005 04:14 GMT > while i can use water bath to get 68F for film development, however, i > found the same method is hard to apply to print development for the [quoted text clipped - 7 lines] > - > narke It's not critical, because you develop to completion.
narke - 02 May 2005 05:04 GMT > It's not critical, because you develop to completion. by 'develop to completeion', did you mean the shortest time for maximal density?
- narke
UC - 03 May 2005 03:22 GMT > > It's not critical, because you develop to completion. > [quoted text clipped - 3 lines] > - > narke The development is more or less self-terminating....
Gregory Blank - 02 May 2005 06:14 GMT > while i can use water bath to get 68F for film development, however, i > found the same method is hard to apply to print development for the [quoted text clipped - 7 lines] > - > narke Steven ; -)
70-72 F to start. although 68F is more likely ambient!
I start a 72F in a tray and use a temp control valve to get there ,...eventually your tray will equalize to the room temp. I find its nice to work faster initially and then work into the ambient temp. :-D
btw couldn't find that plate drawing maybe OMEGA still has it???? If not I could redraw it and send as a PDf if you still want.
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"To announce that there must be no criticism of the President, or that we are to stand by the President, right or wrong, is not only unpatriotic and servile, but is morally treasonable to the American public."--Theodore Roosevelt, May 7, 1918
Ken Nadvornick - 02 May 2005 06:17 GMT > while i can use water bath to get 68F for film development, > however, i found the same method is hard to apply to print [quoted text clipped - 3 lines] > is there a recommended temperature for print development? > and how should i get the temperature? Hi "narke,"
For normal, single-print-per-negative sessions I don't bother with temperature control. I simply dilute my stock D-72 with 68F water and let the temp drift (usually downwards slightly, except in August).
However, for critical sessions where repeatability over time is a concern (such as multiple prints from a single negative) I use a Zone VI Compensating Developing Timer. An attached temperature probe is immersed in the developer tray and the device dynamically adjusts the length of its displayed seconds to compensate for any measured temperature drift of the solution. I can easily judge where the solution is at by watching the seconds tick off and comparing them to the uncorrected wall clock tick in the background. The timer has separate settings for film and paper development.
While some have dismissed this approach as unworkable for various theoretical reasons, in actual use I find that this device does eliminate the lion's share of print variability due to changes in developer temperature. The timer's original developer, Dr. Paul Horowitz, claims "an exponential variation of developing time with [changes in] temperature." If true, this type of feedback correction - similar in principle to the compensating enlarging timers - can be invaluable in certain darkroom situations.
Ken
narke - 02 May 2005 06:39 GMT my room temp in this season is about 82F and keep stable for at least weeks. i believe ice bag is not suitable to be immersed into the tray since it would pollute the solution. and i cannot prepare a water bath for it since if i do so it will need a very large water bath. so what about i do it this way:
do a test to get a Standard Print Time (SPT) for the given temp, and use this time to develop print. since the room temp will keep consistent in a given time of every day, so i guess i do not need to do the test quit often.
would you experts tell me if or not can i do this way?
BTW: I have no idea for what Ken mentioned Zone VI Compensating Developing Timer and i belive i get no way to get it in my country.
- narke
Gregory Blank - 02 May 2005 06:45 GMT > my room temp in this season is about 82F and keep stable for at least > weeks. i believe ice bag is not suitable to be immersed into the tray > since it would pollute the solution. and i cannot prepare a water bath > for it since if i do so it will need a very large water bath. so what > about i do it this way: Buy an water chiller and central air conditioning, or move out of Death Valley!!!
> do a test to get a Standard Print Time (SPT) for the given temp, and > use this time to develop print. since the room temp will keep > consistent in a given time of every day, so i guess i do not need to > do the test quit often. Once is enough provided all factors remain the smame.
> would you experts tell me if or not can i do this way? > [quoted text clipped - 4 lines] > - > narke
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"To announce that there must be no criticism of the President, or that we are to stand by the President, right or wrong, is not only unpatriotic and servile, but is morally treasonable to the American public."--Theodore Roosevelt, May 7, 1918
narke - 03 May 2005 05:57 GMT > Buy an water chiller and central air conditioning, or move out of > DeathValley!!! take easy :-) just the darkroom, my darkroom gets no air conditioner and i can not afford to buy one :-)
-narke
Gregory Blank - 03 May 2005 13:21 GMT > > Buy an water chiller and central air conditioning, or move out of > > DeathValley!!! [quoted text clipped - 3 lines] > > -narke Try ice cubes or a cool water bath under the tray, you probably can't afford a water chiller if you can't afford an air conditioner,...it was just a joke.
 Signature LF Website @ http://members.verizon.net/~gregoryblank
"To announce that there must be no criticism of the President, or that we are to stand by the President, right or wrong, is not only unpatriotic and servile, but is morally treasonable to the American public."--Theodore Roosevelt, May 7, 1918
narke - 02 May 2005 06:42 GMT Hi, Gregory
i'v bought the Omega Enlarger, so i donnot need the draw now. thank you anyway !
- narke
Gregory Blank - 02 May 2005 06:48 GMT > Hi, Gregory > [quoted text clipped - 3 lines] > - > narke Its a great piece of equipment, you"ll be happy for many years :-)
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"To announce that there must be no criticism of the President, or that we are to stand by the President, right or wrong, is not only unpatriotic and servile, but is morally treasonable to the American public."--Theodore Roosevelt, May 7, 1918
Jean-David Beyer - 02 May 2005 11:23 GMT > while i can use water bath to get 68F for film development, however, i > found the same method is hard to apply to print development for the tray > is more large and flat comparing to a tank. my question is, > > is there a recommended temperature for print development? and how should > i get the temperature? I normally process everything at 75F. The usual temperature for processing B&W film and paper is 68F, but it is too difficult for me to maintain this temperature in the summer. I have a Lawlor temperature control valve that does a good job of maintaining a constant temperature provided the cold water is cold enough (a problem in the summer) and the hot water is hot enough (never a serious problem).
I have two darkroom sinks. The big one is about 2 feet by 8 feet. The small one (immediately to its right, and overflowing into the big one) is about 2 feet by two feet. Both are about 5 inches deep. When processing paper, I run 75F water into my print washer that drains into the small sink. The small sink overflows into the big sink. The big sink has a short standpipe in it that maintains a constant depth of water in it that is sufficient to cover the bottom of each processing tray, but insufficient to float the trays when they have processing solutions in them. So this controls the temperature of everything to be about the same.
For film, most B&W processing is recommended at 68F (20C), but for a few developpers, 75F is recommended. There is no great harm these days, with films hardened considerably more than a century ago, to develop at somewhat warmer temperatures. Of course, you calibrate your development time and dilution to give the contrast index you need.
For paper, which is developped "to completion," the temperature is less critical. Within certain limits, you can compensate for having a warmer processing solution (mainly the developper) by exposing the paper slightly less, or developping for a slightly shorter time. Some people develop slightly underexposed paper for a longer time to compensate. For me, these tricks do not work very well.
If you do not keep notes, or change developpers all the time, and make only one print of a negative each session, it does not matter all that much what temmperature you use. If you need repeatable results, you need a stable light source in the enlarger or contact printer, repeatable temperatures and times for exposing and processing, and use of the same (generally fresh) processing solutions. Even then, you may need slight changes from batch to batch of paper.
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narke - 03 May 2005 06:40 GMT Jean-David,
i want you sinks! :-)
- narke
Jean-David Beyer - 03 May 2005 11:34 GMT > Jean-David, > > i want you sinks! :-) I made them out of 3/4 inch exterior grade A/C plywood. I screwed the parts together but applied 2-part resorcinol waterproof glue to the edges first. I then painted them with marine varnish that I mixed 1+3 with thinner so it would penetrate as far as possible. I then applied two coats of Klenk's 2-part Epoxy enamel. Every few years it devellops a slight leak where the wood checks, but these are fairly easily fixed. In those days, the plywood was about US$10 for a 4 foot x 8 foot sheet. It is much more now, but still way less than a new stainless steel sink.
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Gregory Blank - 03 May 2005 13:18 GMT > > Jean-David, > > [quoted text clipped - 8 lines] > was about US$10 for a 4 foot x 8 foot sheet. It is much more now, but still > way less than a new stainless steel sink. That's exactly what I did, mine does not leak, I used silicon boat chalk in the corners and edges prior to painting. I have yet to completely decide wether to deconstruct the sink and reinstall at my new house and darkroom or just start from scratch and build new ones.
 Signature LF Website @ http://members.verizon.net/~gregoryblank
"To announce that there must be no criticism of the President, or that we are to stand by the President, right or wrong, is not only unpatriotic and servile, but is morally treasonable to the American public."--Theodore Roosevelt, May 7, 1918
dan.c.quinn@att.net - 03 May 2005 23:40 GMT > ... sinks! The sink for a good darkroom need be large enough to wash up and no larger. It is a good idea to have a water proof counter area for processing. I wonder what is the purpose of the deep, wide, long sinks some have. These days I process single tray using dilute chemistry which is always fresh each print. One tray processing uses very little room. As for temperature, keep your developer a few degrees cooler with a well placed SMALL fan. Dan
narke - 04 May 2005 08:49 GMT dan.c.qu...@att.net wrote:
> > ... sinks! > [quoted text clipped - 3 lines] > I wonder what is the purpose of the deep, wide, > long sinks some have.
> These days I process single tray using dilute chemistry > which is always fresh each print. One tray processing uses > very little room. how did you do one tray processing? as far as i know, i will need seperated trays for stop, fixing and wash. so i totally need 4 trays to get a final print.
> As for temperature, keep your developer a few degrees > cooler with a well placed SMALL fan. Dan Lloyd Erlick - 04 May 2005 13:08 GMT ...
>how did you do one tray processing? as far as i know, i will need >seperated trays for stop, fixing and wash. so i totally need 4 trays to >get a final print. ...
may405 from Lloyd Erlick,
Single-tray print processing is a convenient work- and time-saver. You most certainly do not need four trays to get a final print.
I've often wished I had adopted single-tray work before I bought all those trays! I have a collection of small, medium and large trays waiting for the day my print washer dies and I have to drop back to tray-washing!
I have an article on my website about single-tray print making. It's under the 'technical' button on the table of contents.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
Rod Smith - 04 May 2005 17:42 GMT > Single-tray print processing is a convenient work- and time-saver. You > most certainly do not need four trays to get a final print. For those who are short on horizontal space, there are also vertical processing trays. I ran across a description here:
http://silvergrain.org/Photo-Tech/Nova-Monochrome.html
I've never used the product described, though, so I can't say how well it works or how it compares to single-tray processing. I just ran across the URL and thought it was an interesting concept, although not one I personally need to use.
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Nicholas O. Lindan - 04 May 2005 18:49 GMT > You most certainly do not need four trays to get a final print. Darn straight. I figure you need ten:
Darkroom: 1 Developer 2 Stop 3 1st fix 4 2nd fix 5 Holding bath
Post process: 6 Ferricyanide bleach 7 Post-bleach fix 8 Rinse 9 Hypo Clear 10 Toner
Plus a couple extra for water bath development, Selectol soft, a second toner ... and they make dandy seed trays for starting the tomatoes, marigolds, nasturtiums, sunflowers, cosmos and snapdragons early, and for washing off the dog's muddy paws. Figure twenty-four trays or so should do you.
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Pat OBrien - 05 May 2005 04:21 GMT How many breakfasts does a Hobbit have before 11 am? And could ya start Weed seedlings in a single tray process or should they sprout first?
Lloyd Erlick - 05 May 2005 13:38 GMT >> You most certainly do not need four trays to get a final print. > [quoted text clipped - 19 lines] >snapdragons early, and for washing off the dog's muddy >paws. Figure twenty-four trays or so should do you. may505 from Lloyd Erlick,
Starting seeds has to be the best reason for multiple trays! What about a squeegee for the garden??
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
Andrew Price - 05 May 2005 23:04 GMT >Starting seeds has to be the best reason for multiple trays! What >about a squeegee for the garden?? Only if the drying screens can come along, too ...
dan.c.quinn@att.net - 10 May 2005 11:14 GMT > > You most certainly do not need four > > trays to get a final print. > > Darn straight. I figure you need ten: If I processed the usuall way I would need at least six: Developer, stop, fix 1, fix 2, hca, rinse- holding. I'd be stuck with 5 x 7s. Working with one tray I've room for 16 x 20s. Dan
Lloyd Erlick - 10 May 2005 13:53 GMT >> > You most certainly do not need four >> > trays to get a final print. [quoted text clipped - 5 lines] >holding. I'd be stuck with 5 x 7s. > Working with one tray I've room for 16 x 20s. Dan may1005 from Lloyd Erlick,
I bet you've got room for a 20x24 tray! And I bet you could switch back and forth at whim, in the middle of a session.
regars, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
David Nebenzahl - 05 May 2005 02:49 GMT On 5/4/2005 5:08 AM Lloyd Erlick spake thus:
> ... >> how did you do one tray processing? as far as i know, i will need [quoted text clipped - 12 lines] > I have an article on my website about single-tray print making. It's > under the 'technical' button on the table of contents. You know, I've been hearing about this single-tray method for a while now, probably about every other time Dan Quinn posts. I have to say that it strikes me as a lot of extra work for little gain--for *most* darkroom work. (With exceptions--see below.) It means an incredible amount of pouring liquid in and out of trays--once for each different bath used for each print. For a klutz like me, who finds it difficult to pour my fixer back into its gallon container at the end of a printing session without spilling all over the place, it would be a frigging nightmare. No thanks. (This from someone who generally limits himself to 8x10 prints.)
As Lloyd points out in his article, the one exception I would grant to this would be processing large prints (say larger than 11x14); then, it could well be easier to pour liquid in and out of the tray, rather than wrestle the print from tray to tray.
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dan.c.quinn@att.net - 05 May 2005 04:44 GMT > RE: David Nebenzahl wrote: > > For a klutz > like me, who finds it difficult to pour my fixer back into its gallon
> container at the end of a printing session without spilling all over the > place, it would be a frigging nightmare. No thanks. (This from someone > who generally limits himself to 8x10 prints.) I think you must have a wrong picture in mind. There's nothing to it. The developer goes in the tray then the paper, or papers if batch processing. When developed, the tray with print or prints held in, is emptied. As you are aware I use chemistry one shot. So, in my use the tray's chemistry goes down the drain. I've not yet missed the sink. Ditto for fixer. I see no reason for a stop bath given the one-shot use and the highly dilute near neutral fixer. And, BIG PLUS, archival results with one fix. So, in and out with the developer, in and out with A fix, and you've a print or prints ready for an archival wash routin. If there are more to follow then a holding tray makes for two. I've no stored working strength solutions. The very dilute developer does need more time. Five minutes is my usual limit. Most of the above applies to one-shot processing. Dan
Lloyd Erlick - 05 May 2005 13:57 GMT David Nebenzahl wrote:
>> For a klutz >> like me, who finds it difficult to pour my fixer back into its gallon [quoted text clipped - 4 lines] >someone >> who generally limits himself to 8x10 prints.) ...
may505 from Lloyd Erlick,
I thought tray wrangling would make single-tray work impossible for me, too. But it's nothing at all, really, and I commonly use 16x20 and often 20x24.
The tray is placed on a stand in the sink (or countertop). The height of the stand is such that the mouth of the storage jug for a given solution is at the level of the bottom of the tray. To pour solutions back into the storage jug, the corner of the tray nearest the jug rests on the stand. The other corners are gently lifted toward the jug, tilting the tray while it rests on the near corner. Slowly the solution drains into the jug, until finally only a fraction of the liquid remains, at which point it is no challenge to lift the tray completely and drain it completely.
Pouring solutions back into the storage container from the tray is actually a very low-skill, low-practice matter. It's in the same category as tying shoe-laces - easier to do than to write about.
I found some four-liter storage jugs with wide mouths (four inch) so they make an excellent pouring target. They originally held cat food. They are storage jugs (caps on) for solutions between sessions, and working containers (caps off) during a printing session.
Not many people would be klutzier than I am. I couldn't live with a Beseler 4x5 enlarger because I kept hitting it with my head, knocking it out of alignment. In the past, the prospect of lifting a tray full of solution and attempting to pour it into a jug was indeed a nightmare. But the way I've worked out for doing it obviates all difficulty. At no cost! The stand can be a scrap of plywood standing on some bricks, or anything that comes to hand.
I like to be able to put my storage jugs in their own individual water baths. I keep developer at 21C and selenium toner at 32-34C. I also like to be able to switch paper sizes at will. Swapping the tray for a different size is a snap.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
narke - 06 May 2005 04:00 GMT > may505 from Lloyd Erlick, > [quoted text clipped - 7 lines] > liquid remains, at which point it is no challenge to lift the tray > completely and drain it completely. how many times do you reuse your dev, fixer? i noticed you pouring back all of them to their original container every time. how do you think use a diluted solution and then simply drain them out after processing?
- narke
Lloyd Erlick - 06 May 2005 15:08 GMT >> may505 from Lloyd Erlick, >> [quoted text clipped - 14 lines] >- >narke may605 from Lloyd Erlick,
Usually I limit my developer working solution to two sessions. My general pattern is to have a day of general work on some specific pictures to establish my ideal way of making them. Then I would probably have a day in which I produce the final prints, in however many copies I need. The day of experimenting would probably be done with the previous session's developer, if only a day or so had gone by. The day of making final prints would be with a freshly mixed working solution of developer. (I mix my developer directly to a working solution from dry powder chemicals. I don't like to store solutions if I can avoid it.)
I re-use my fixers until two-thirds the maximum number of prints have been processed. I like to use sodium thiosulfate based fixer because it has no smell issue, and it is relatively low capacity, so I can more or less use it up without unduly long storage. Kodak mostly specifies a maximum of twenty-five 8x10s or equivalent through each liter of fixer. I like to make up three liters, because that is a convenient volume for me. It implies seventy-five 8x10 prints, so two thirds would be about fifty, which are equivalent to about twelve 16x20s. I use a double-bath setup for fixer, so in reality I only use my fixer to one-third capacity, since I never promote my second fix to first place because it is so cheap and easy to prepare fresh fix. Anyway, I am hyper-conservative about my fixer use because I want no chance of stains on my prints. Fixer is cheap, but each sheet of 16x20 costs me nearly five dollars.
I've never used dilute, one-shot solutions for making prints. Dan Quinn calls it the LFP method (Least Fluid Practical). The single-tray method is ideal for this type of work. It's even simpler, because there is no need to pour solutions back into their storage containers. The tray can simply be upended in the sink. So the huge difficulty of pouring out of a tray back into a jug is removed. Sort of like Velcro for the shoes instead of laces, such complicated things to tie up!!
But the LFP method has a significant advantage - no finished print has been exposed to used chemicals. Every print is made with freshly mixed solution, so no secondary products have had a chance to build up in any of the solutions. In other words, the fixer never builds up silver complexes due to more and more silver being removed from successive, multiple sheets of paper. Washing prints should be as easy as it is possible for it to be.
Don't forget that these techniques are merely refinements of the old standby technique of many trays and stored solutions. I adopted the single tray method because I find it less work. Cleanup is simpler, and it eliminates the mid-process holding tank or tray.
I like to be able to view a print that I have fully toned, in case I want to change the enlarger exposure on succeeding prints. I don't like to store prints in a holding tray and tone them all in a batch later. I'm sure to find the final print tone wrong that way. I also, personally, hate to stack prints in a tray and shuffle them over and over each other. I hate to see fine scratches on my prints when they are dry and finished, and shuffling them while they are wet seems like a sure way to scratch them to me. I've seen a pattern of very fine scratches on gallery-displayed prints quite frequently, by observing the surface of the print at close range, by very oblique light. (Craning the neck and touching the glass with the nose may be necessary...). Usually the scratches are in a vaguely oval pattern, suggesting sloshing about in liquid. My overall "philosophy" of print making is that the face of the wet print shall be touched by nothing at all, except at extreme edges and corners. So the backsides of other prints may not touch any print faces.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
dan.c.quinn@att.net - 07 May 2005 00:04 GMT > I've never used dilute, one-shot solutions for making prints. Dan > Quinn calls it the LFP method (Least Fluid Practical). The single-tray [quoted text clipped - 5 lines] > > ... the LFP method has a significant advantage - no finished print has
> been exposed to used chemicals. Every print is made with freshly mixed > solution, so no secondary products have had a chance to build up in > any of the solutions. In other words, the fixer never builds up silver > complexes due to more and more silver being removed from successive, > multiple sheets of paper. Washing prints should be as easy as it is > possible for it to be. Having been at it a while I think I'd characterise the method as being the one tray-one shot method using the least fluid practicle, LFP. So, the OT-OS method using the LFP. Practicle not Possible as the least possible would be less solution volume than would allow for easy handleing. Generaly speaking, solution volume must be minimal if concentrations are to be reasonable and frugal use of chemistry be made. I'm not about to suggest a method which wastes chemistry. On an 8 x 10 basis I've found 250ml to be plenty and 125ml as little as I care to work with. With that little amount FB paper should be pre-wet. A Camera and Darkroom article from a few years ago recommends a flat bottom tray when single tray processing. Dan
> Don't forget that these techniques are merely refinements of the old > standby technique of many trays and stored solutions. I adopted the [quoted text clipped - 19 lines] > > regards, le narke - 07 May 2005 09:38 GMT dan.c.qu...@att.net wrote:
> > I've never used dilute, one-shot solutions for making prints. Dan > > Quinn calls it the LFP method (Least Fluid Practical). The [quoted text clipped - 56 lines] > > > > regards, le Ken, thanks for giving such a funny/interesting story.
- narke
narke - 07 May 2005 09:53 GMT i think i'v got some basic idea about LFP by reading your posts. now i belive i am so interested on it and has an itch to try. but it seems i need a considerable more detailed introduction or step by step guid for the mothod. is there an url dedicated for that? thanks!
- narke
dan.c.qu...@att.net wrote:
> > I've never used dilute, one-shot solutions for making prints. Dan > > Quinn calls it the LFP method (Least Fluid Practical). The [quoted text clipped - 56 lines] > > > > regards, le narke - 07 May 2005 09:15 GMT from what you described, i conclude that your process is actually a one shot kind with no dilution.
> >> may505 from Lloyd Erlick, > >> [quoted text clipped - 90 lines] > ________________________________ > -- dan.c.quinn@att.net - 04 May 2005 23:21 GMT > dan.c.qu...@att.net wrote: > [quoted text clipped - 12 lines] > > > ... a well placed SMALL fan. Dan Single tray processing is the same as rotary processing. The chemistry is poured in then poured out. The only difference is that a tray is used rather than a tube. Do you know anything about rotary processing? Tube or tray the chemistry can be one-shot or it can be saved for more prints. I use the chemistry very dilute and the least fluid practical, then toss after one use. Advantages with one-shot are fresh, known strength solutions each print; no bookeeping or testing of used solutions needed. I keep a few small bottles of premeasured stock or concentrate on hand. At processing time I make the final dilution. There is little work to test the method if you wish. For an 8 x 10 tray use 250ml solutions and wash waters. Dilute your stock or your concentrate developer twice then four times as much as usual. Develop each test five minutes then dump the developer and pour in the fixer. Do not Stop. For A. Thiosulfate at 1:39 dilution, fix for 2 1/2 minutes constant agitation. After fix and for RC I suggest three washes, 1, 2, and 3 minutes. S. Thiosulfate will also work, and quickly with prints, but I've not tested for that. I currently use straight A. Thio. at 1:49 dilution for 2 minutes but that is on a specific paper on which tests have been made. Two BIG PLUSES come with one-shot high dilution fixer. BIG PLUS one is the great number of prints per unit concentrate. BIG PLUS two is the archival results achieved with one fix. Dan
narke - 05 May 2005 10:35 GMT dan.c.qu...@att.net wrote:
> Single tray processing is the same as rotary processing. The > chemistry is poured in then poured out. The only difference is [quoted text clipped - 21 lines] > PLUS one is the great number of prints per unit concentrate. BIG > PLUS two is the archival results achieved with one fix. Dan i am not sure what is the proportion you dilute the developer and fixer. would you please fill in the table below (by replacing those x's)?
for D-72 Dev ------------- dilution: 1:x approx development time: x minutes
for F-5 fixer ------------- dilution: 1:x approx fixing time: x minutes
- narke
dan.c.quinn@att.net - 06 May 2005 11:05 GMT > i am not sure what is the proportion you dilute the developer and > fixer. would you please fill in the table below (by replacing those > x's)? Do you intend to compound that developer and that fix or will you buy it at the store? If you will be compounding those two yourself I should know the formulas you are using. I may not have the same formulas as you have. Also, the method I suggest allows for a more simple formulation. What chemicals do you have for compounding a developer and a fixer? Dan
narke - 06 May 2005 13:57 GMT dan.c.qu...@att.net wrote:
> Do you intend to compound that developer > and that fix or will you buy it at the store? compound myself.
> If you will be compounding those two yourself I > should know the formulas you are using. I may not > have the same formulas as you have. > Also, the method I suggest allows for a more simple > formulation. What chemicals do you have for compounding > a developer and a fixer? Dan i plan to use Kodak D-72 as print developer, and since i'v already got chemicals for Kodak F-5 fixer, i will so like to also use it as print fixer. below are formulas of them,
Kodak D-72 ---------- Water 750 ml metol 3 grams sodium sulfite (dessic) 900 grams hydroquinone 12 grams sodium carbonate (monohydarted) 80 grams potassium bromide 2 grams water to make 1 L
Kodak F-5 ---------- Water 600 ml sodium thiosulfate 240 grams sodium sulfite 15 grams 28% acetic acid sol'n 48 ml boric acid (crystals) 7.5 grams potassium alum 15 grams water to make 1 L
BTW: I see some source say that for F-5: Shelf life: stores for at least one week
what that exactly mean? should I store F-5 for a week before use them? it sounds weird.
- narke
Lloyd Erlick - 06 May 2005 15:47 GMT ...
>i plan to use Kodak D-72 as print developer, and since i'v already got >chemicals for Kodak F-5 fixer, i will so like to also use it as print >fixer. ... may605 from Lloyd Erlick,
Kodak fixer formula F-5 is of academic curiosity only, these days. It was superseded by F-6 long before I was born!
F-5 stinks powerfully of sulfur dioxide. It attacks the mucous membranes of the respiratory system. Your education will be advanced by making up some F-5, but you don't need a gallon or even a liter. Make a quarter liter and you will see (or smell...) what I mean.
F-6 is utterly odorless once the alkali is added to the mix, so it's much easier to work with. The formula mixes perfectly well if the alkali is added before the acid, although the formula usually indicates acid first. It's just that if the acid goes first, the stink rises immediately, until the alkali is added. Alkali first means no stink at all.
But for modern photosensitive materials of the sort used in a regular darkroom, hardening is easily replaced by normal care on the worker's part (that would be me...). In the F-6 formula, with the exception of sodium thiosulfate and sodium sulfite, all of the ingredients are present for hardening the photosensitive coating. I long ago eliminated hardener and acids from my darkroom. F-6 without hardener or acid is nothing but sodium thiosulfate and sodium sulfite in water -- which is a formula that Ansel Adams included in the appendix of his book, "The Print". He called it 'plain fixer'. I have been using it for years and it is perfect for my purposes. You're going to think I'm weird, but I use distilled water to make up my fixers. Tap water contains things I don't know about, so I'm suspicious. I have to use a sequestering agent like Calgon if I use tap water, so right there a cost is obviated by using distilled water.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
Ken Nadvornick - 06 May 2005 18:52 GMT > F-5 stinks powerfully of sulfur dioxide. It attacks the mucous > membranes of the respiratory system. Hi Lloyd,
The description seems a bit over the top to me. In my case one of the great joys of darkroom work is precisely the subtle smell imparted by an acid type fixing solution. I've worked for many years as an amateur (and for several years professionally as a custom B&W printer in the 80s) surrounded by this smell and without any respiratory ill effect whatsoever.
I compound all of my chemistry from scratch and so could select any fixer type I desire. I choose Kodak F-5 (wherever process-feasible) simply because I enjoy the smell. No other aspect of my darkroom work is more powerful in its ability to mentally transport me back to my youth.
So I guess we're all different.
Ken
P.S. Interesting story...
Last week I was volunteer teaching a class of 8th-graders (~14 years old) how to build and use pinhole cameras. We exposed paper negatives in one-gallon paint cans and then made contact prints.
After his processing was complete one of the boys - Ben - came up to me and asked about the smell on his hands after washing up. I grinned and told him it (the smell of F-5 fixer) was harmless and would last about 24 hours and that he should consider it a badge of honor. I said he had now taken his rightful place in the long unbroken line of analog film/darkroom photographers stretching back over 150+ years.
He looked at me suspiciously, then left. I found out later that he had subsequently searched out all of the other 8th-grade girls and had them smell his honor-drenched F-5 hands. Don't know if he got any dates out of this novel approach, but I don't think that using an acid-based fixer to get the girls is documented anywhere in Kodak's literature... <grin>
narke - 07 May 2005 09:26 GMT > may605 from Lloyd Erlick, > [quoted text clipped - 5 lines] > by making up some F-5, but you don't need a gallon or even a liter. > Make a quarter liter and you will see (or smell...) what I mean. yes i learn formula from book. i knew that f-5 smells, but i did not know so serious it is. thanks, i will switch to f-6!
> F-6 is utterly odorless once the alkali is added to the mix, so it's > much easier to work with. The formula mixes perfectly well if the [quoted text clipped - 27 lines] > ________________________________ > -- Lloyd Erlick - 07 May 2005 14:21 GMT ... i knew that f-5 smells, but i did not
>know so serious it is. thanks, i will switch to f-6! ...
may705 from Lloyd Erlick,
Well, try it out at least once ... maybe you'll like it!
For me, the 'subtle' smell of fixer comes from non-acid fixer. It is mild and practically fragrant, to me. That, and the smell of a just-opened package of paper, are the smells of the darkroom. I hate it when the smell of something clings to my body. I don't even like to use perfumed soap, or those paper things that get thrown in the laundry dryer.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
dan.c.quinn@att.net - 07 May 2005 11:43 GMT > i plan to use Kodak D-72 as print developer, and since i'v already got > chemicals for Kodak F-5 fixer, i will so like to also use it as print [quoted text clipped - 9 lines] > potassium bromide 2 grams > water to make 1 L That D-72 formula looks OK except for the sulfite. I think it should be 45 grams. Where did you find that 900 grams? If your scale will do it, I suggest you mix no more than a 1/3 batch. My scale's good to .01 gram but I weigh no less than 1 gram. If you have small trays, 5 x 7, use 125ml of D-72 at 1:3, 1:5, and at 1:7 dilution. Develop each test print for 5 minutes. Reasonable exposure is up to you. You will find that a more dilute developer will require a little more exposure. Take note of the amount of time for first appearance of an image. The more dilute the more time. Keep in mind you are testing.
> Kodak F-5 > ---------- [quoted text clipped - 5 lines] > potassium alum 15 grams > water to make 1 L Unless you just want to use up your chemistry I don't recommend F-5. A S. Thio. plus S. Sulfite fix has been suggested. I've taken that one step farther and have used just S. Thio. Either way is OK with one-shot use. Your S. Thio. is likely the pentahydrate. If that be the case and on an 8 x 10 basis, dissolve 9 grams in 250ml H20. If you've the anhydrous, use 6 grams. Fix for 3 minutes. Constant agitation and flip now and then is the way I do it.
When fixing use the solution volumes I've mentioned for those two size of prints. For archival results with one fix the solution volume must be reasonably great. The capacity of a fixer is based on the amount of silver per unit VOLUME. The gram quantities suggested allow a little margine of excess chemistry; enough to handle even an unexposed paper. Dan
> BTW: I see some source say that for F-5: > Shelf life: stores for at least one week [quoted text clipped - 4 lines] > - > narke narke - 08 May 2005 02:29 GMT dan.c.qu...@att.net wrote:
> > i plan to use Kodak D-72 as print developer, and since i'v already > got [quoted text clipped - 13 lines] > That D-72 formula looks OK except for the sulfite. I think > it should be 45 grams. Where did you find that 900 grams? If your yes, it's my faults. 900 grams is for 20L solution.
> scale will do it, I suggest you mix no more than a 1/3 batch. > My scale's good to .01 gram but I weigh no less than 1 gram. > If you have small trays, 5 x 7, use 125ml of D-72 at 1:3, > 1:5, and at 1:7 dilution. thanks for those start points. but you missed dilution for 8x10, let'me gues, a 1:2?
> Develop each test print for 5 minutes. > Reasonable exposure is up to you. You will find that a more dilute [quoted text clipped - 14 lines] > Unless you just want to use up your chemistry I don't > recommend F-5. why do you think those other ingredients are of no use? you method only use one ingredient in original F-5.
> A S. Thio. plus S. Sulfite fix has been > suggested. I've taken that one step farther and have used [quoted text clipped - 11 lines] > gram quantities suggested allow a little margine of excess > chemistry; enough to handle even an unexposed paper. Dan - narke
dan.c.quinn@att.net - 08 May 2005 06:12 GMT > thanks for those start points. but you missed dilution for 8x10, > let'me guess, a 1:2? > > why do you think those other ingredients are of no use? you method only > use one ingredient in original F-5. The dilution is the same no matter the size. Solution volume is increased as the size of the print is increased. For staters use 125ml for 5 x 7 and use 250ml for 8 x 10. It is only the thiosulfate that does the fixing. The sulfite is a preservative. Unused sodium thiosulfate solution when kept in full sealed bottles will last months. The amount used one-shot has only minutes of use in the tray and then is down the drain. Those other ingredients are for ph adjustment and ph buffering. They make the fix acid and keep it that way. Acid fix is not so needed with today's emulsions because they are pre-hardened. So, those ingredients are not needed. Also, with no acid fix to keep acid you will not need an acid stop bath. I don't bother with stop bath because the fix is used only once. I have added a 1/10th part of sulfite to the amount of thiosulfate for longer lasting fixer. The sulfite will make your fixer alkaline. Dan
narke - 08 May 2005 07:41 GMT okay. let repeat the whole thing and make sure i dont make any mistake:
TITLE: the one shot one tray method in paper processing
DEVELOPMENT 1, make original Kodak D-72 solution. 2, every time before processing, dilute the original solution to 1:3, 1:5 or 1:7 as work solution. 3, for each dilution you choiced, do a test to get proper exposure time. 4, for 5x7 tray, use 125ml diluted solution, for 8x10 tray, use 250ml diluted solution. general rule is that a bigger tray, a more work volume.
STOP no stop is needed since we will not reuse fixer.
FIXING 1. no storage solution. 2, every time before processing, put 9 grams sodium thiosulfate into 250ml water (you said H2*0*, did you mean H2*o* here?) for 8x10 tray, hence 4.5 grams into 125ml water for 5x7 tray.
am i right? when compond the one shot fixer above, is there any temperature requirement?
- narke
dan.c.quinn@att.net - 09 May 2005 01:49 GMT > okay. let repeat the whole thing and make sure i dont make any mistake: > [quoted text clipped - 9 lines] > diluted solution. general rule is that a bigger tray, a more work > volume. I'll tell you how I now go about it and suggest a starting point. IF I were to mix up a full batch of D-72 that batch would have a volume which would fill 4 bottles. The total volume would be 1 liter give or take a little depending on your bottles. I keep ALL perishable liquid chemistry in FULL bottles. Then 3 of the 4 bottles are stored. The one other bottle of 250ml, give or take a little, is split into 4 bottles. Those 4 must hold that 250ml. Depending on your bottles, you may need to add a little water, H2O. My rule is, when spliting one bottle to more, be sure the more bottles will hold all or a little more than the one bottle. I've not diluted yet. So, give or take a little, I've 3, 1/4 liter, 8oz, bottles stored and 4, 1/16 liter, 2oz, bottles ready for work. For an 8x10 to process and at a 1:3 dilution I add a 1/16 liter bottle to 3/16 liter H2O; 250ml. In practice I use a glass beaker. A little water goes in then the stock strength develper. The mix is poured into a 250ml bottle and the bottle topped up. The mix then goes back into the beaker and the beaker emptied into a parafined paper cup for a tray's serving. Likely I'll go for the 1:7 dilution for starters. I think good results will be had with 5 minutes in the developer. That means one of those 1/16 liter, 2oz, bottles will be split to two. The method may seem involved but once the chemistry is mixed and the first split made, things move right along. And, fresh chemistry, one-tray, and the used chemistry gone. The same applies to the fix. Mix up a small batch and then do the split or splits. I process at room temperature; 21 to 24 centigrade. Let us know how it goes. Dan
> STOP > no stop is needed since we will not reuse fixer. [quoted text clipped - 9 lines] > > narke narke - 09 May 2005 02:53 GMT got it. i will do the practice next month and report the results. print paper and some gears still on purchasing. i am currently considering which kind of easel and paper cutter/knife i will need.
- narke
dan.c.qu...@att.net wrote:
> > okay. let repeat the whole thing and make sure i dont make any > mistake: [quoted text clipped - 54 lines] > > > > narke Lloyd Erlick - 08 May 2005 14:18 GMT ...
>> > Kodak F-5 >> > ---------- [quoted text clipped - 11 lines] >why do you think those other ingredients are of no use? you method only >use one ingredient in original F-5. ...
>narke may805 from Lloyd Erlick,
My fixing method uses three of the ingredients from the above formula for F-5 fixer -- Water, sodium thiosulfate, and sodium sulfite.
The remaining ingredients are hardener or hardener-related -- acetic acid sol'n, boric acid, potassium alum. Potassium alum is the hardener, and a hardener will work only in an acid medium, so acetic acid is used. Boric acid is a buffer and helps keep the pH of the fixer within a certain range appropriate to the hardener.
I have decided to forego hardener in my darkroom because I have never had a problem with scratches on my film or prints. I am a one-person operation and I just handle my materials with ordinary care. Present day materials are quite robust and survive very well if one exercises a normal level of care. In fact, I believe films are hardened during manufacture. The T-Max films are designed for automated processing at 100 degrees F, so it's pretty easy to be careful enough there. My prints are made by hand, by me, and not even in total darkness. Easy to be careful there, too. I've had no trouble from eliminating acid from my darkroom. In fact, things are now easier and cheaper, and much more comfortable. I've written about all this on my website.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
narke - 09 May 2005 02:58 GMT read over the article -- processing Fiber Base Prints with Ansel Adams' Odorless and Cheap "Plain Fixer" from Bulk Chemicals.
thanks. the method a little differ with dan.c.qu...@att.net's, you add sodium sulfite, he remove sodium sulfite, you use undiluted, he use diluted. but i understand, that is same basic idea behind.
- narke
> ... > >> > Kodak F-5 [quoted text clipped - 47 lines] > ________________________________ > -- narke - 09 May 2005 03:06 GMT another question, Lloyed,
does the plain fixer suitable for film process? and will you suggest that?
- narke
Lloyd Erlick - 09 May 2005 14:34 GMT >another question, Lloyed, > [quoted text clipped - 3 lines] >- >narke may905 from Lloyd Erlick,
Yes, plain fix does perfectly well for film. I've used it to fix my film for several years. I use a double bath setup for film (and paper too). This means I make up two separate working solutions of fixer, and fix my film for equal times in each fixing bath.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
dan.c.quinn@att.net - 09 May 2005 23:50 GMT > another question, Lloyed, > > does the plain fixer suitable for film process? > and will you suggest that? I've also used the plain fixer for several rolls of Pan F+. IIRC, Mr. Erlick uses that fixer for TMAX films. We both shoot 120. For Pan F+ I've had very good results using 22.5 grams sodium thiosulfate penta-hydrate, 15 grams anhydrous, in 375ml of solution; 10 to 12 minutes. One-shot of course and that was for Pan F+ Sulfite does at least two things for A. or S. thiosulfate. It extends the life span and it makes the fixer alkaline. I can do without the sulfite because I use fixer one-shot. I compound my own chemistry and can choose what chemicals to use. If you feel safer with sulfite, add sulfite. Likely I'll do some more testing with sulfite added and make carefull note of the times needed to fix. Dan
narke - 10 May 2005 01:51 GMT THANKS! hope you and Erlick publish more and more data (fixing time, formula, dilution) about one-shot(non-one-shot) plain fixer on film processing.
- narke
dan.c.qu...@att.net wrote:
> > another question, Lloyed, > > [quoted text clipped - 15 lines] > Likely I'll do some more testing with sulfite added and > make carefull note of the times needed to fix. Dan Lloyd Erlick - 10 May 2005 14:26 GMT >> another question, Lloyed, >> [quoted text clipped - 4 lines] >Pan F+. IIRC, Mr. Erlick uses that fixer for TMAX films. >We both shoot 120. ...
may1005 from Lloyd Erlick,
Yes, I mostly use T-Max 400 (TMY). I've also fixed Agfa APX films, Ilford D3200, and lots of Tri-X, too (in 120 format, TX and TXP).
A sodium thiosulfate-based fixer is sometimes claimed to be incapable of fixing tabular grain films, but I have found this to be incorrect. The capacity of a sodium thiosulfate based fixer is smaller than an ammonium thiosulfate fixer. This only means the fixing baths must be retired sooner, or after a smaller number of rolls of film have been processed. In reality this is an advantage, not a drawback, since I am only one person and I do not use such huge numbers of rolls. Once in my life I have exposed a hundred rolls in one month; my average would be well below that. My fixers tend to get used up long before they get old. Also, plain fixer based on sodium thiosulfate is very cheap, so tossing it before it comes to its absolute final end is not a problem.
I use a double-bath fixing setup, and I fix tabular grain films for six minutes in each bath. It's easy to compensate for the lesser efficiency of sodium thiosulfate in fixing tabular grain film by fixing for an appropriately longer time, and by making sure the baths are fresh.
I know Dan Quinn uses ammonium thiosulfate in his process, but I have found sodium thiosulfate much easier to procure. The best deal I could find on ammonium thiosulfate was a forty-five gallon drum of sixty per cent solution. The seller would not break it down into twenty liter pails (wouldn't crack the seal on the drum). They wanted sixteen hundred dollars (Canadian) for it, so I passed. I buy sodium thiosulfate anhydrous in hundred pound bags, and since 1998 the price has remained about C$130. I can just go to the seller and pick it up, so I don't have to factor much shipping into that price.
In general, over the years I've found that ordinary darkroom practice includes a little more complexity than necessary. The usual lineup of multiple trays is a good example. It's just not necessary. Fixer is another example. At this late date, hardener is a specialized material and technique. Ordinary darkroom work pretty much does not require hardener (I have used no hardener for almost thirty years). Fixer that contains no hardener is very simple and cheap. It's almost a badge of honour for some people to have a stinky darkroom where your nose and eyes can get bitten. I certainly don't think this is necessary, and I have found it is perfectly possible and easy to have an odorless darkroom. In fact, its cheaper than the stinky way.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
Lloyd Erlick - 06 May 2005 15:18 GMT ... the method I suggest allows for a more simple
>formulation. ...
may605 from Lloyd Erlick,
This seems like a very substantial advantage. Easier to prepare solutions, and cheaper to prepare.
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
Lloyd Erlick - 04 May 2005 12:58 GMT ...
> I wonder what is the purpose of the deep, wide, >long sinks some have. > These days I process single tray using dilute chemistry >which is always fresh each print. One tray processing uses >very little room. ...
may405 from Lloyd Erlick,
Well, I agree with you in theory, but a nice large sink is a fine thing!
I like to work single-tray too, and I find myself swilling out my tray very frequently - water rinse instead of acid stop bath, lots of water rinse after selenium toning, etc. - and it's convenient to just upend the tray in the sink. I suppose I could say I use my sink as if it were a large waterproof counter-top, except that it connects to a drain so I can be pretty wet about things.
And my only reason for having yet another sink, a big double-tub restaurant style stainless affair with a built-in shelf at the left side, is that I got it for a song (or free, I forget, it was thirty years ago). I find it convenient for developing film.
You can't have too much film, or too many sinks ...
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
pgg - 03 May 2005 03:16 GMT I don't understand why you would need any temperature control with print developers because prints develop "to completion".
In the winter, my basement darkroom gets down to 55 degrees and I noticed no difference in my prints.
> while i can use water bath to get 68F for film development, however, i > found the same method is hard to apply to print development for the [quoted text clipped - 7 lines] > - > narke Peter De Smidt - 03 May 2005 04:23 GMT > In the winter, my basement darkroom gets down to 55 degrees and I noticed > no difference in my prints. I've found the opposite to be the case with the materials I use, namely Zone VI print developer and Ilford FB MG paper. I'm not a chemist, but it's my understanding that some developing agents become inactive below a certain temp. Hence I try to keep my print chemicals at around 70* F. I use a kaiser photographic hotplate under the developer, and heating mats for under seedlings under the other trays. I find that if I keep my basement darkroom air tempature at a normal level that my solution temp dips down into the mid 50s in winter.
-Peter
Francis A. Miniter - 03 May 2005 05:08 GMT > I don't understand why you would need any temperature control with print > developers because prints develop "to completion". [quoted text clipped - 13 lines] >>- >>narke As Peter mentioned, below certain temperatures, some developers cease to act. There are some charts in The Darkroom Cookbook that you might want to look at. There are even developers specially formulated for low temperature processing.
In the winter my darkroom is also about 55 degrees. I use two electric heaters to warm it up to the mid-60s, partially for comfort, partially so that I do not have to wait forever for the processes to complete. I do not bother with a water bath for B&W printing. I do, however, for color printing.
One advantage, I believe, from development at colder temperatures is the reduction of fog. So if that is a concern, work in the cold.
Francis A. Miniter
narke - 03 May 2005 06:01 GMT > I don't understand why you would need any temperature control with > print developers because prints develop "to completion". if development is self-terminating, why people bother to do 'stop' ?
-narke
Jean-David Beyer - 03 May 2005 11:37 GMT >>I don't understand why you would need any temperature control with >>print developers because prints develop "to completion". > > if development is self-terminating, why people bother to do 'stop' ? It is _not_ self terminating. If you leave a print in a developer too long, the whole thing will turn black. Before that, the fog starts to increase to give unacceptable highlights.
It is less critical than film development, especially since if you goof with a print, you can reprint, whereas making a new negative may be impossible.
 Signature .~. Jean-David Beyer Registered Linux User 85642. /V\ PGP-Key: 9A2FC99A Registered Machine 241939. /( )\ Shrewsbury, New Jersey http://counter.li.org ^^-^^ 06:35:00 up 9 days, 12 min, 3 users, load average: 4.17, 4.17, 4.08
jjs - 03 May 2005 13:25 GMT >> I don't understand why you would need any temperature control with >> print developers because prints develop "to completion". > > if development is self-terminating, why people bother to do 'stop' ? In an acid process, the stop helps keep the fixer fresh.
If it is so hot in your darkroom, what would concern me first is your film developing problems. There is a whole body of literature on developing film in hot conditions. If you cannot find it online, then I'm sure some of us can look to our own resources for you.
Cold weather development is my problem. FWIW, one can develop film in developers under 0C (32F). I'd be happy to keep the darkroom over 50F.
LR Kalajainen - 03 May 2005 20:37 GMT I cut my teeth on hot-darkroom photography in Borneo. Even with a room air conditioner, couldn't get the temperature under 83 to save my life. Ambient water temperature was 85. Gave me grain the size of basketballs. That's when I discovered (through an old Dignan Photographic newsletter) the technique of divided development. The time/temp variable disappears. By using a variant of D-76 divided for film development, I got my grain under control, and I've continued to use divided development for printing since it permits greater contrast control than single-solution developer (by using a "soft" Bath A to lower contrast and a "hard " Bath A to raise it), it cannot overdevelop, and it gives absolute repeatability in multiple prints from the same negative. It will, however, make you a better printer, in that any major manipulation must be done under the enlarger. But while frustrating at first, that's all to the good.
> > [quoted text clipped - 16 lines] > > narke - 04 May 2005 10:34 GMT thanks for all your replies.
while got so many information and hints around the concern, i found, however, all your opinions add up to a point which makes me hard to draw a conclusion. if that is not a problem of my understanding, there must be a contradiction somewhere. below is my thinking:
1, on one hand, if paper developing is a function of time and temperature, and one factor can compensates another. so under a given room temperature, one can do a test to get a SPT(standard printing time), and use the SPT for development. some people agreed with this method.
2, on the other hand, some people use special equipments, developers and processing methods to confront with hot or cool aimbient temperature.
here a contradiction rised, if 1 is valid, why some people bother to do 2? does this contratiction means that while 1 works, that however can not promise a quality resulting?
- narke
Lloyd Erlick - 04 May 2005 13:28 GMT >thanks for all your replies. > [quoted text clipped - 19 lines] >- >narke may405 from Lloyd Erlick,
These are really two different approaches to the same problem, not two contradictory concepts. Each method would work, in the sense of yielding satisfactory prints.
Since I work single-tray, my chemical solutions are kept in separate containers. I find it very simple to stand my developer in a water bath (OK, ya caught me! I use one or two of my surplus trays to hold the water bath!) In winter, I stand my developer in its own water bath, and my fixers and hypo clear baths in another bath. I find it very easy to keep my solutions at 20-21C when my darkroom is around 12-15C (or even lower...). I keep a thermometer in my developer jug (my nice process thermometer) and a cheaper one in the first fixer jug.
Here's a little challenge for 'Narke'. Without spending another minute, or another penny, go to your darkroom and set up and make some prints. Any time a barrier appears, fix it and continue. Solve each impediment as it appears, and keep a list of what you've done. Use the list to address each problem later in a more permanent way if necessary. Work through each and every problem until fine prints result. This will very likely entail frustration and outright failure at the beginning. One thing about the darkroom, it sure teaches one to accept deferred gratification...
regards, --le
 Signature ________________________________ Lloyd Erlick Portraits, Toronto. voice: 416-686-0326 email: portrait@heylloyd.com net: www.heylloyd.com ________________________________
narke - 05 May 2005 08:14 GMT > may405 from Lloyd Erlick, > [quoted text clipped - 24 lines] > regards, > --le good suggestion, thank you! and i'v checked the article about single-tray on you site. i am going to read ...
- narke
narke - 04 May 2005 10:47 GMT thanks. I'v read your article, it seems interesting and reasonable except lefting some questions for me:
1, your divided formulas all use teaspoon as unit. it's amazing to me! your teaspoon may differ with mine. could you tell me how many grams for a teaspoon?
2, you also give formula for ilfochrome. as far as i know, ilfochrome refers to a special process which use special chemical and specail paper for transparence printing. did you mean, the special ilfochrome chemical can be substituted by the formula you given? in the case, what paper i should use? normal color paper or still ilfochrom classic paper?
3, is the divided method wildely acceptable? i noticed that there are not many people in the group adopt this technique as their prefer processing method. as a newbie in darkroom, i am very careful in processing choice. anyone has any idea about this?
thanks again.
- narke
> I cut my teeth on hot-darkroom photography in Borneo. Even with a room > air conditioner, couldn't get the temperature under 83 to save my life. [quoted text clipped - 3 lines] > time/temp variable disappears. By using a variant of D-76 divided for > film development, I got my grain under control, and I've continued to
> use divided development for printing since it permits greater contrast > control than single-solution developer (by using a "soft" Bath A to [quoted text clipped - 20 lines] > > > > Rod Smith - 04 May 2005 18:09 GMT > thanks. I'v read your article, it seems interesting and reasonable > except lefting some questions for me: I'm not the person to whom you've addressed your questions, but I do have a bit to say....
> 1, your divided formulas all use teaspoon as unit. it's amazing to me! > your teaspoon may differ with mine. could you tell me how many grams > for a teaspoon? That depends on the substance being measured. To take an extreme example, a teaspoon of neutronium would weigh a heck of a lot more than a teaspoon of styrofoam. ;-) I must have missed the formula, so I don't know what's in it and can't say what the conversions are. I'm sure there are references with this information, but I don't have pointers offhand, except that I *THINK* Anchell's "The Darkroom Cookbook" has conversion tables. (I've ordered a copy, but it's not arrived yet.)
More generally, some people just like using teaspoon (or other volumetric) measures for darkroom chemistry formulas. Patrick Gainer has been known to advocate this approach -- he wrote a published article on the topic some years ago. His more recent formulas all seem to use gram measures, though; I don't know if he's soured on volumetric measures or is just giving the masses for the masses, as it were. ;-) If a formula is given in teaspoons, I'd just use that measure.
As to consistency, if you use appropriate measuring spoons, there shouldn't be much of a problem. Just be sure you don't confuse English vs. US measures. I don't know about teaspoons, but for some units, they vary across the pond. Of course, this means using actual measuring spoons, not the sort of spoons you'd use for shoveling Wheaties into your mouth. ;-)
> 3, is the divided method wildely acceptable? i noticed that there are > not many people in the group adopt this technique as their prefer > processing method. as a newbie in darkroom, i am very careful in > processing choice. anyone has any idea about this? In my (still very limited) experience, it seems to me that there are all sorts of variant methods that are perfectly "acceptable." Individuals might prefer one method or another for their own idiosyncratic reasons (they want particular types of results; they're limited in space, funds, or whatever; they're familiar with a method; etc.). If something looks interesting to you and there aren't major hurdles (like the purchase of a $100,000 piece of equipment), try it. If you like it, keep using it. Of course, it's best to go about these experiments methodically -- keep using a technique for long enough that you feel you've got some sort of a handle on it, and be consistent while you do so. Changing half a dozen variables every time you step into your darkroom will make it very hard to learn anything.
As to divided development specifically, I don't believe it's a weirdo fringe technique. I suspect, but don't know, that it's not more common simply because it takes more effort than using a single developer.
 Signature Rod Smith, rodsmith@rodsbooks.com http://www.rodsbooks.com Author of books on Linux, FreeBSD, and networking
Nicholas O. Lindan - 04 May 2005 18:57 GMT "narke" <steven@lczmsoft.com> writes:
> 1, your divided formulas all use teaspoon as unit. it's amazing to me! > your teaspoon may differ with mine. Nope. The 'teaspoon' is a standard measure - measuring spoons, not the spoons for drinking tea.
Measuring spoons are: faster, less error prone, less likely to spill dry chemicals all over everything, cheaper ($0.79 Vs $79.00 for a balance), don't need filter paper on the balance pan, can be used in a pinch when you can't find the set in the kitchen.
 Signature Nicholas O. Lindan, Cleveland, Ohio Consulting Engineer: Electronics; Informatics; Photonics. To reply, remove spaces: n o lindan at ix . netcom . com psst.. want to buy an f-stop timer? nolindan.com/da/fstop/
Peter Irwin - 04 May 2005 19:45 GMT > "narke" <steven@lczmsoft.com> writes: > [quoted text clipped - 3 lines] > Nope. The 'teaspoon' is a standard measure - measuring spoons, > not the spoons for drinking tea. A US teaspoon is about 4.93ml.
The teaspoon measure used in most other English speaking countries is 5ml. The difference will not normally matter. A set of plastic kitchen measuring spoons is very handy for measuring small amounts of various powders and liquids.
Peter.
 Signature pirwin@ktb.net
narke - 05 May 2005 08:26 GMT > That depends on the substance being measured. To take an extreme example, > a teaspoon of neutronium would weigh a heck of a lot more than a teaspoon [quoted text clipped - 3 lines] > except that I *THINK* Anchell's "The Darkroom Cookbook" has conversion > tables. (I've ordered a copy, but it's not arrived yet.) i am now so regret my posting of such a foolish question about teaspoon, it make me looks like a chemical idiot, and unfortunately i am!
the url below will point you to the original formula of divided developer: http://www.apug.org/forums/article.php?a=87
i still like someone give me a converted mesure unit since i'v already spent money on a balance and for such a chemical idiot as me it is hard to go down streat and find a store selling starndard measuring spoon.
> As to divided development specifically, I don't believe it's a weirdo > fringe technique. I suspect, but don't know, that it's not more common > simply because it takes more effort than using a single developer. anyone gets any other idea about this subject ?
- narke
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