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Photo Forum / Film Photography / Darkroom / May 2005

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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.

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

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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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 - 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 :-)

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

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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Rod Smith, rodsmith@rodsbooks.com
http://www.rodsbooks.com
Author of books on Linux, FreeBSD, and networking

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.

Signature

Nicholas O. Lindan, Cleveland, Ohio
Consulting Engineer:  Electronics; Informatics; Photonics.
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psst.. want to buy an f-stop timer? nolindan.com/da/fstop/

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
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________________________________
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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.

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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
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________________________________
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voice: 416-686-0326
email: portrait@heylloyd.com
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________________________________

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.

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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.

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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.
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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