Rochester Institute of Technology RIT Scholar Works Theses Thesis/Dissertation Collections 11-1-1981 Investigation into the mechanism of development to increase exposure latitude without loss of threshold speed Susan A. Egnoto Follow this and additional works at: http://scholarworks.rit.edu/theses Recommended Citation Egnoto, Susan A., "Investigation into the mechanism of development to increase exposure latitude without loss of threshold speed" (1981). Thesis. Rochester Institute of Technology. Accessed from This Thesis is brought to you for free and open access by the Thesis/Dissertation Collections at RIT Scholar Works. It has been accepted for inclusion in Theses by an authorized administrator of RIT Scholar Works. For more information, please contact [email protected]. l!Wt$TlCATIOll llITO TIl! I£ClWIISJl: OF llllVlLOfllDlT TO lllCll%ASE I.XPOSUU I.\TITtltll 1ll'l'llOUT LOSS or tBl.SIIOlIl --.'''' ........ s:PUl) SUsClfl A. EWlOlO _ _., '.tbotoaraphlt Stl~. _ In... - -...10Cl Burt H. GamlII ........................................... llt. 1.11. Carroll Ronald Frands .................. llt. l. rnnt!o School of Photographic Art. and Sclence. RochuUr Inati.uta of TechtlololY Roehe.t.r, Nov York CERTIFICATE OF AFPllIVAL MASTER'S TllE.SIS Thl. i. to eertify thot the Maate.'. The.i. of Suoon A. Eanoto hu be.., e....inod. and approved by tile thuh co-inee U ooUabotory for tha ,h.. h requlrement for tho Ma.ter of Seionoe dogree. Boo H. Canoll ................................ Or. II. K. l4rroll Grall! Hais! ...... Il'r. _ EIlg.lmann ... ~,~J.H"~ Dara ElIQelmaoo _ . . Cit 0' " c' A ~ : _orr-con J1llY o T',; D '.1 .. ,. .or INVESTIGATION INTO THE MECHANISM OF DEVELOPMENT WITHOUT LOSS OF THRESHOLD SPEED TO INCREASED EXPOSURE LATITUDE by Susan Egnoto Submitted to the Photographic Science and Instrumentation Division in partial fulfillment of the requirements for the Master of Science degree at the Rochester Institute of Technology ABSTRACT A ing the by mechanism developed to undertaken was study loss altered through variations quinone toe of agent high contrast Developer speed. the and concern emulsion is latitude, exposure properties bromide in pH, concentration, information were ion concentration, Phenidone */hydro- ratio. The tration gain significantly increased a without developing a which to is the latitude and suggests that throughout indicate that results the toe The speed. experimental the bromide reduces exposure produced primarily *Ilford trademark. range. changes bromide ion concen factor reducing both the predominant the the the The rate other in development 11 of exposure evidence development facts investigated rate without latitude affecting the and exposure silver are at a sufficient given that so the until contrast, exhaustion of rate available occurs. The ability to without loss relatively exposure of toe constant range, and increase depends speed rate the of having useful upon maintaining development no 111 soluble scale exposure over bromide the a desired present. TABLE OF CONTENTS AUTHOR'S CLARIFICATION OF CHEMICAL COMPOUNDS AND SYMBOLS USED IN THIS MANUAL v LIST OF TABLES LIST OF vi ILLUSTRATIONS vii I. INTRODUCTION 1 II. THEORY 5 5 8 10 11 The Characteristic Curve Development Rate of Development Exposure Diffusion Developing Agent Concentration Bromide Ion Concentration 12 12 13 13 14 15 pH Covering Power Developer Formulations III. 17 EXPERIMENTAL 17 19 Experiments Extended Experimentation Preliminary IV. Effect Effect Effect Effect of pH of Developing Agent Concentration of Hydroquinone of Bromide Ion Research Additional V. 29 DISCUSSION Concentration . .... 32 38 41 47 54 59 CONCLUSIONS 61 BIBLIOGRAPHY iv AUTHOR'S CLARIFICATION OF CHEMICAL COMPOUNDS AND SYMBOLS USED IN THIS MANUAL Several research have, shortened is of chemical for simplicity, form throughout this listed below manual the with the compounds been used referred The text. corresponding in this in to full version a correct used form in this . Formula Chemical Name Form Used in Manual Sodium sulfite (desicated) Na2S03 Sodium borate Na2B40? Sulfite 10 (H20) Borax Sodium carbonate Monohydrate Kodalk* Na2C03 H20 Carbonate balanced alkali NaB02 Potasium bromide KBr Kodak Micro-File Recordak Film Type ^Registered 4 (H20) 5454 Trademark of Kodalk Bromide Microfile Eastman Kodak Co. v LIST OF TABLES TABLE from the Literature I. Developer Formulations II. Preliminary III. Experimental Design 21 IV. Exposure Data 22 V. Exposure Latitude, Speed, and Gamma Listed as a Function of Development Time for the Various Developer Formulations 30 VI. Covering Experimental Design ... 16 18 57 Power vi LIST OF ILLUSTRATIONS FIGURE 1. Microfile developed in D-19 for 1, 2, 4, and 6 minutes. Numbers on the curves indicate development time in minutes 2. . Microfile developed in POTA for 4, 5, 7, 9, and 11 minutes. Numbers on the curves indicate development in minutes time . 3. 4. Microfile developed in POTA + Kbdalk for 2, 3. minutes using 4x5 inch trays. Numbers on the indicate development time in minutes. Microfile developed in POTA for 2 and 3 minutes, using 8x10 inch trays. Numbers indicate development time in minutes 5. 4 and curves . Microfile developed in POTA for 5, 7, and 9 minutes Numbers indicate development using four 35mm tanks. in minutes time . 6. Development POTA 7. Change of rate (). Numbers Microfile processed in D-19 () indicate various exposure levels. in development rate with Numbers indicate 8. opment O for 4 . Change tion of 9.7); 10. = for 3 minutes Change tration at 4 and A g/1. POTA + ?= = 2.0 A= minutes; + carbonate A POTA = POTA + carbonate Phenidone concentra ? and , devel 11 and 4 minutes; and = g/1. with for pH with Solid for 3 pH .4 minutes. VII = 3 minutes minutes with curve POTA + Kodalk for for a POTA + Kodalk for carbonate in development = minutes various 7, 9, . in development 2.5 for 3 levels. exposure for pH's POTA for = developer several various different Solid line POTA + borax times. minutes; + Kodalk 9 developed Microfile for pH formulations. and the (pH bromide = (pH 10.6). = concen POTA + borax for 5 minutes; and 8 D= POTA 11. Change in development with pH with the Hydroquinone concentration 1.0 g/1. Solid curve POTA + borax for 3 and 4 minutes; A POTA + Kodalk for 2 and 3 ? POTA + carbonate for 1% and 2 minutes. minutes; = = = = 12. Increased developer exhaustion with pH when the Phenidone concentration =0.5 g/1. O POTA + borax for A 5 minutes; POTA + Kodalk for 5 minutes; and ? POTA + carbonate for 4 minutes = = = . 13. Change in development in Phenidone concentration at two No symbol =1.5 g/1 Phenidone + Kodalk for a 4 minutes; 2.5 g/1 Phenidone + Kodalk for 3 minutes; 2.5 g/1 Phenidone + carbonate for 2 minutes; ? 1.5. g/1 Phenidone + carbonate for 3 minutes. pH levels. = = = 14. Change in development rate as for 4 pH levels. a levels 15. in development a rate [Phenidone] /[Hydroquinone] A of Phenidone indicate exposure . Change 1.0 function Numbers concentration as function ratios of of 0= for pH 1:3 and 1:1. = Both have a Hydroquinone concentration Numbers indicate exposure levels. g/1. = 16. Change in density and maximum slope as a function of development time for processing in POTA + Kodalk + Numbers indicate exposure values. Hydroquinone (1:1). 17. in development with various ratios of Phenidone POTA for 7 and 9 Solid curve = a and for 4 5 minutes; [1.5] [1.0] minutes; Change to hydroquinone. = = [0.5]/I1.0] 18. for 3 and 4 minutes. in development with bromide ion concentration POTA for 7 minutes; Solid curve pH. A POTA + POTA + 1 g/1 bromide for 10 minutes; a POTA + Kodalk + 1 g/1 bromide Kodalk for 4 minutes; T POTA + Kodalk + 2 g/lbromide for for 4 minutes; Change at = constant = = = = 5 19. minutes. development time for development with and A= A POTA + Kodalk; POTA + Kodalk bromide. Numbers indicate exposure levels. + lg/1 bromide. Density vs. = without 20. Development levels 21. Slope of vs. rate pH. log vs. concentration Numbers exposure indicate of bromide at three levels. exposure for 7-minute development in POTA. Vlll 22. Slope 23. Change vs. in addition A 24. Mg = log slope of as A= POTA + Kodalk + 1 ment silver/ft (O) D-19 as and 6-minute development in D-19 function a bromide. 2 of for exposure a g/1 log exposure bromide for 4 function () of with the POTA + Kodalk for 4 minutes; POTA. IX of minutes. density for develop I. Several in the which INTRODUCTION latitude exposure increased considerably 1-3 The conditions. in which 5454 toe the to compared 2. and a high to is the narrow grain The contribute to effect. could be exposed It related grain 1 over two, development fine grain, (Table 1) useful exposure conditions scale. of scale of characteristics as monodisperse relatively exposure of 1 Figures in D-19, processing loss without in POTA developer this of propose was to from research in developer ability to the the by Levy of a changes ultimately to work will The yield ability this emulsions emulsion with distributions. size and the factor a general purpose specific what development specific was was Kodak Microfile Film Type considerably increase the contradicts emulsions past of narrow and gamma certain the latitude recommended under of of in undertaken interesting conventional Microfile film that by use processed when speed, by most exposure increased was have been studies a was composition increase reasonable exposure postulated the in the one developer 1 to hinder, that to this developability another , or latitude, mechanism originally change investigate to explain effect of developer an exhaustion and effects that in covering changes lation. Each factor relation to, or can occur power effect the upon, through introduced into variations in the development careful D-Log E investigation has development curves, levels, exposure forum varying developer interpretation Therefore, the with for chosen high at of a known process. the changes information concerning process can be deduced. CU & P e O co U QJ CM w 0) T-l u 0 a H e ^ co T3 QJ a -y fi 0 CO -J- T-l E . <" C -H r-l QJ S !=> 0 H O m H -u w o . o o ON 4-> pH - X fi QJ 1 w O B u o H r-l T) cu > Pi C o QJ h4 cu CXT3 o rH QJ QJ 4-> > Cd QJ O T3 -H id QJ fi rH H H <4-l CO O QJ H > O U rl fi S o i-l QJ rl OC . |CN r-l r-* bO r-l Cn Aiiswaa o co r-l Q) CO QJ 4-> fi fi H e i^H CO I Q) a fi. 8 fi H e ON c H QJ in <t J-J o 14-1 QJ e << Pa H O O Ph QJ > fi QJ *fi QJ QJ 4J PiCtj O O i-t'i-l QJT3 > fi QJ *fi -H co CU OJ > H 5-1 14-1 O fi O H O QJ H^ (U 5-1 fi bO H Aiiswaa II. THEORY The Characteristic Curve In the image" describes upon occurring grain is, the branches concerned the The theory first The with amount more the of the the density is curve in which result an increase may be and area, in covering can the be to the in the of image be can the latent The grains. proposed in the 5 of as density number under which logarithm some in the fraction power in considered increase although variations halide curve," the against histogram unit image formation which that distinct Two grain. research, branch has been conventionally "characteristic per render latent a by grain density received. exposure the of will relationship between developed through The of "latent halide which mechanism pertinent second exposure. the of term silver criterion silver The plotted in the latent of the sense radiation sole is within is which second, to developability formed is change exposure in the separated. and that developable. then, image fundamental most of silver. of a developed incident frequency is usually the developed grains circumstances each studied grain there developed, is 6 For the of the photographic development let present, are (Q) a grain is , which will in terms which means of the that render by Q a single same value number spread sensitivity Q, of the simplified variations of composition but will view the of Q of absorbed, log It has been a of spread in results for units of be described cannot values sensitivity grains in fact have 2.0 to quanta halide silver and 1.0 the developable. grain distribution This values. size of a describing of determined experimentally that nominally the consider omitted. The conventional of in process process us a a size o class of fluctuations in quanta attributed mostly the This grains. grain latent received the will The term of Q, where developable Such 11 values quantum ' 1 9 per random be formed. by a (on plotting is the unit measurements for of individual that with distribution" Q vs a of of area, processes values. . proportion absorbtion due to the part but random can be occur within a stable which g "sensitivity describe this distribution statistically in determine the efficiency that image to is spread Q the size sensitivity distribution Q for of This all grains quanta) is and is 1. = of values become which Ea to shown observed distribution classes used Q indicate that the is relatively independent of grain the the until size, of efficiency silver sites traps competing for the Too many traps latent image generated during in the formation of none sites, initiating development. probability of quanta, and will, tion to the image, they more sensitive Farnell a in where a spread note is the of that a as tribution, grain the , size the the a of contribu in general is given be and n is From this larger, i.e., spread of a the G. g 2 2 = a C. of + 2 n sensitivity relationship wider the by spread sensitivity relationship: spread class. sensitivity number larger a concept same by size make of grains. the g becomes a specific small have grains of exposure. many capable therefore, will, of layer, single a he defines which grain single larger development, smaller Another view is which absorbing upon than of Because greater number electrons result will that so developable latent to aggregation enough* is decreased due to the increased image sub- become large grains dis grain layer we increases accordingly. If we distribution corresponding now of consider grain ^Approximately than 1.0 p 2 sizes, of ranges a an emulsion it will contain sensitivities. mean grain has that An projection a wide grains emulsion area with of this greater type will than an u *- but ion. have a emulsion greater range a containing light of narrower (latitude) response grain distri- size 14 Development discussion The preceding tion that quanta once per a unit grain has become developable. would scope and must be now a latent stable This assump of it image, limited has assumption include the development to modified the upon the minimum number absorbed form to area based was process. From is solution If a a silver a a reducing halide solution, the reduction long of barrier, to be that thermodynamic period be completely time, of silver must exchanged. decreases It this be is silver is barrier in rate.16 reaction Thus discriminate between upon the difference the ability unexposed in the rate and of a order of and of such favor the for left halide silver by halide. with If electrons presence height will metal. retarded overcome the of silver contact the all Transfer ions in put developer a view, unexposed equilibrium halide to reduced. which is of point for agent emulsion silver enough developer to electrochemical an would from the potential for energy electrons latent image the increases the development to exposed areas reduction of depends the two 17 areas. is It now formation is the sites the on reduction act Hamilton and F. indicate to a some The Urbach The are which at general ( the of the and of set from the therefore necessary specific able. speck In fact probability of speck The processing it is between develop the the of to a may vary the one develop of specific render and will 19 thought grain a is It that a develop development over a considerable 20 . sizes. variation conditions exposure latitude increase is in zero sites height altered. that shown by original to required has been varies . r range size the to modify and are conditions better. or principle development conditions, considerably if those % site. ability indicate that the latent image is given for the developable may not developmental results specific define the term determined is at developable all not development times, barrier 18 probability developability potential, potential sites metal catalysts developer. and develop. as the definition implies that develop, silver of reaction "developable" ment of which crystal, J.F. This production latent image that accepted generally in the developability is factor one obtained part the by Levy result of in the and of grains with increased others. preferential 1-3 This differences 10 in the rate different Rate latent image The overall metallic rate Because the area is not as rate of development change exposure. readily development is of is silver time. produced mass of silver measured as A density with An example of optical density arises such with unit per silver produced rate of silver formation may be of thorough discussion following overall considerable exposure and tion grains, covering rate number received, 2) species into other of or shown plotting given in Figure increase 6 and in the decrease in 21 A silver. is a in D-19 the by masked the rapidly than the the area, unit however, because more power at given more in the section. The a of by processed developed the is this method, may increase less power density, optical curve a of covering per development time for mass the rate produced is commonly illustrated in problem the increasing develop with for Kodak Microfile Film Type 7460 POTA. containing sizes. ment the grains Development of which development between of the 4) developing the of development of factors; diffusion the the gelatin agent reduction 22 of and 1) of influenced level the the ions the species to by of developing layer, 3) other silver is agent adsorp AgX to metallic silver, 11 5) influence the diffusion and/or diffusion of factors these a) halide layer. account the of It hydration and 7) and emulsion, is necessary to take comparing development when the all rates. Exposure As of development the reaction high because the unit grains increased, the therefore, more agent consumed final result development contributing teristic as the as a number and time in factor exposure the Ives in decrease of factor increases, development with to fewer rate exposure shoulder be formed. in this is rate of are with the is one charac that left unexposed; region less, The is This considered grains is developing more exposure. occurring increases, in development the This exposure also products high forming Another differentiation grains of developing of of amount oxidation areas reaction number 23 regions exhaustion. is reduced, halide more a the exposed of silver may be curve. result As volume. unit the upon in the composition grains. chemical of amount is dependent time per developing the due to local developer exposure results per of developer the formation the continues, development may be limited in that out pointed process alters products immediate vicinity the out developer through of 6) reaction, ions gelatin into form oxidized chemical the the of swelling the of again is high but resulting 12 in the formation of the of development depends shoulder. b) Diffusion The tration opment are rate the various of consumed and the proceeds, in grain and a chemical products site within products emulsion, When the out. considerably higher than that tion the of the rate state , layer c) reactants not generally of be the chemical concentration same products in as reaction may be and reactants of within at occurs diffuse must the the concentra emulsion within low, will ". However, sufficiently established are development is solution. is development products reaction diffusion, of as a . .if steady the ..25 agent In general, increasing has been shown should to plotted vs. agents. be the concentration the of rate development development agent If this obtained when logarithm of relationship the increase will Equation concentration. describe the relationship 9 fi developing line and rate reactants which ... Developing with reactants of Because this the in reaction concen The devel solution. formed, therefore, concentration changing. continuously the is process in components the upon logarithm developer for several holds, of 1 the a straight rate concentration. is 13 R Cs = a = concentratin fraction a d) Bromide or development. the lower regions. exposure 27 induction agent one in will more than will the rate also through a greater image effect increase of rate in effect in the higher has the an latent of decrease in the a have than regions Bromide period it decrease the general When bromide causes density formation, of (1) ion concentration fog formation of AC^ developing of Soluble bromides rate = exposure increasing in the the barrier charge effect. e) pH Activity no change in will increase ionization, paraphenylenediamine: contain the as when there with developers such as However, for ionizable hydroxyl groups, active species increases, the will concentration The the ionization curved arrows of of the the ionization Phenidone indicate pH developing be dependent increase according to the where even with agents concentration upon active As pH. species the is that of pH will constant. is shown movement of in Equation electron 2, pairs 14 ionization The for Phenidone is defined constant Equation by 3. 0=C fS=C CH92 I | H-N < CH92 CH02 "*| -H+ > \N/ CH02 \ C6'H5 K = "II | <:N: CH02 :6-C 4 .N / > | U) CH02 v \ / N N C6*5 C6H5 [P"][H+1 (3) [P] Covering Power The produced varies predominantly the silver under will the a of development with solution-physical formed be will be filamentary. density they optical of method density produced defined as optical density from the ratio and development conditions, a given D/M, in silver differ The covering change in the image 29 measured silver produced solution-physical low activity developers is It the of in is power is of greater of D where amount may be formed silver. mass ment silver of is the Since the the amount M area. 1 types produce. In contrast, particles. measuring the of unit others, two silver Under conditions. compact These developed the direct development conditions, convenient and form characteristic per develop used by Levy o than in the conventional processes, it will 15 be necessary to take this factor into account. Developer Formulations Developer increase exposure trends may be one developing ing two note that than those which latitude listed in Table 1. observed investigation. also formulations First, of ratios of Metol primary the 31 the It was concentration developing range only 1 of agent. 8 to of 9. Metol Metol factors the It is formulations. developing therefore contain 30 considered are and remain hydro respect to the The developers also operate at a contain no soluble bromide and - to vary meaningful with and to ratios hydroquinone of only Phenidone not for higher These mixtures, agents the interesting hydroquinone to General chosen Phenidone; or to used developers the superadditive or primary pH at most g/1. From the review the three conventional in the quinone. suggest hydroquinone. indicate that are which either agent, contain the are have been preceding studied: the of discussions, concentration these four of developer factors Phenidone Phenidone to hydroquinone ratio, and the formulations were and pH. chosen of to bromide, and be the 16 TABLE from the Literature Developer Formulations POTA D/23 1.5 Phenidone 30.0, Sulfite I g/1 Metol g/1 Sulfite D/25 7.5 100.0 g/1 Metol R/l Sulfite NaHSOo TEA- 14 Phenidone A Hydroquinone Sulfite KBr Polyethylene Glycol Triethanol Amine ^Sulfite = sodium sulfite T/0 1.1 g/1 .5 g/1 4.0 1.0 2.0 20. g/1 g/1 g/1 ml (desiccated) 7 g/1 100 R/l 5 0 15 0 g/1 XDR-4 g/1 Sulfite 1.0 1.0 25.0 KHCOo 10.0 g/1 Metol Hydroquinone g/1 g/1 III. EXPERIMENTAL Preliminary Experiments Preliminary determine to in change what 3 Table Unfortunately, the emulsion chosen exposure The pH. 9.68. and pH of varied strip 20C was with were were Kodalk at 10 at 50 g/1 made seconds standard tray was g/1, 30 g/1, 90 give attenuator 17 by indicated agitation. a g/1 using three at used no rock in below: given g/1 produced to and g/1 the EG&G developed for the time show g/1 with with not g/1 obtained Borax systems. 10~3 at pH did outlined formulation is Buffer carbonate sodium is experiment 1 5 1 10 in and monodisperse concentration sulfite Metol Hydroquinone KBr Sulfite 8.03. Exposures #99603, of complete variations different buffering a levels sulfite Kodak High Resolution was The base developer The produce 3 at a to attempt developer formulation the as scale The film tested S0343, II. of of of values concentration an latitude altered. Film Type in run the would any increase in was the extent were affect pH emulsion. experiments pH 10 a g/1 pH of of 10.55. sensitometer in place. in Table to R.I.T Each II, at 18 TABLE Preliminary II Experimental Design pH BORAX (low) KODALK (med) CARBONATE (high) 10g/l SULFITE CONC 30g/l . 90g/l 8 4 any combination This could showed results of be the and sulfite of result act as to hydroquinone the secondary was pH, in factors, In chosen. sufficient developing it while hydroquinone possibility may be exhibiting this that effect. is this Metol agent; This implies of which ratio is will The exhausted. emulsion the speed. of for hydroquinone to 31 erated in one at scale exposure shifts only several is the developer formulation Metol -n.) increase no 4 2 1 (ma TI>IE The 8 4 2 16 be other incapable that regen- factors of such as 19 grain composition, mide, and specifically chlorobromide variations tributing factors in composition with in the ability to size obtain iodobro- vs. may be con increase in an scale. To could insure that be obtained, a results similar Microfile Film Type 7460 sensitometer in place. at 23 C R.I.T. The strips similar to reduced without those 5, of with and a toe Figures 1 and 2 Levy1 those was of Kodak run. Kodak Model a neutral 101 filter density developed in POTA developer 7 The minutes. speed, actually increased the toe speed) of to using 2.1 by Levy, obtained loss exposed then were for 3, D-19 and experiment was #02570, similar the contrast (in this as results shown were being POTA experiment by the comparison . Extended Experimentation The matrices experimental which vestigated were centration, Hydroquinone the are the concentration ratio could the be to obtained. base formula in variation in of Phenidone concentration combinations pH was consisted in Table outlined A development 36 design time insure and the series that of III. of The factors in Phenidone, bromide concentration all obtained con to pH. was run comparisons for at each changes were made, using the buffers the of contrast equal The POTA developer formulation which 3x4 three, was and the outlined in 20 the preliminary error determined from was in explained replication of experimental the of preparation base developer formulation. the of processing A measure experiments. detail more in the processing This and is section. Exposure All exposures R.I.T. sensitometer, 7460, a with combination strips 2 in g/1 were values for the except which The a neutral .3 step densities and listed in Table 4. are processed 101 Kodak Microfile Film Type onto substituted. exposure corresponding exposed was at Kodak Model the with density filter, bromide with made #02570, neutral .8 filter density were five within minutes The .after exposure. Developer preparation One each liter Starting combination. distilled water developer of the solution approximately 750 with chemicals were in the added sulfite, Phenidone, hydroquinone, buffer, allowing each the next. out the For amounts with an to chemical Several chemicals, accuracy of depending + gram .005 and for ml of order: bromide, dissolve completely before adding different balances less than 1 prepared was upon were the amount the Torbal grams was used to being weight weighed. balance, #126240 used. Amounts less 21 Q) 4-) cd fi o rO rl cd o ^ CO r-l QJ CO T3 s 3 o H ^ 4-1 C QJ fi E W) Pa o H CO IH QJ M M P rH QJ X rH W CO kJ 4-> PP fi <! H QJ w & > cd QJ u o M P e H rl QJ P, X W r-l cd o a r-l r-l rH rH rH r-\ ^. M M to bO m r-l M O bO r-i iH r-i n cn r-l rH bO CN CM 1 O QJ o H fi H P o 4-1 cdT3 rl U -H fi fi QJ QJ fl O P^ fi O MH C; o i i CJ JH'H g c o fi fi QJ o rl *fi 0 H cr Ctj*fi +-> 1 OJ ^ fi *H O fi o c o O QJ u H .fi fi fi 4J PL| OMH cd C3 o Pc QJ U O PQ i i >1 w 1 22 TABLE IV Exposure Data Illuminance at wedge = 1700 Exposure time = Exposure at = 340 = 2.53 Log .20 wedge exposure at wedges lux sees lux-sees Log Step # 1 2 3 4 Density .06 1.67 .22 1.51 .37 1.36 .52 1.21 5 .68 6 .81 7 exposure 1.05 .92 .78 .95 8 1.10 .63 9 1.23 .50 10 1.36 .37 11 1 48 .25 12 1.62 .11 13 1.76 1.97 14 1.90 1.83 15 2.05 1.68 16 2.20 1.53 17 2.33 1.40 18 2.49 1.24 19 2.66 1.07 20 2.83 2.93 21 3.03 2.70 . 1 23 5 than grams #126239, which chemicals #108634, were which The 1 to off were is weighed is liter. #62629 standardized out accurate The were pH a to to + then The remaining grams. .05 . 1 grams. cooled measured was pH + balance, using the Dial-O-Gram balance, 25C, at at the Dial-O-Gram on accurate solutions Meter R.I.T. and weighed after 25C to topped and using the Beckman the meter calibrated was 10.0. of Processing This the true spirit Although those section no encountered time the series of remaining a was convenience, A 4x5 agitation. four 35 mm solution the data film was were was the was without The were for initially time and inch tray and which development required repeatable as exactly only 250 However, tried. shown chosen tray continuous could a ml of upon pro periodic first processing method, with for and develop a allow the influencing error. anticipated, combination, would in out delay Because each which tray development initially trial method, headaches. needed carried was greatest required strips not problems greatest strip strips. scientific caused cessing technique removal the processing that matter, ment of the research of of for rock accommodate processing replication, in Figure 3. 24 bO C iH CD QJ CO 9 4-1 4-1 C QJ S Pa O T3 ro cu > . CU <N 4-) }H cd o o m -rl ^J fi r-H H ro Tl CO o QJ > rl + fi o < C/j H QJ o Ph Ph 4J X w fi rl o o XI QJ Pa QJ CQ -1 QJ fi fi >S QJ CU CO "-1 rl 4H O b Cd rl 4J 8-5 CO OJ rl CO . CM fi bO rl fe Aiiswaa 25 It of the strips ference seemed from the lie in using to 1000 Following ml of small tray interactions between caused effects solution. with believed that the was sides the of larger tray a line this processing solution and more processing 8x10 inch tray an tried Once again, "bigger better" and solution 2 then liters showed no increase method of processing lopment tank to a technique with 2 liters and At apparatus this point, is very uniform, required time these and without it a is reasons, this to shifted one liter of The results the tray rock of 4x5 inch the use still thirty every were once again of volume method to and seconds. unusable. method developer remove remaining was simultan the nitrogen burst of Although this the solution deve^ taped was moving the holders up of impossible a Each strip immersed into the use large removing and solution. seconds method considered. was of consisted from this results tried was then down continuously for ten The solution. was abandoned. was next Agitation of method inch tray, in repeatability, 4x5 inch holder eously. 11x14 an with and The the processing Figure next. 4 indicates that the improvement in repeatability negligible. inter and The remedy tray. was closeness strips thought, of and only strips considered as of agitation is solution one strip well. only as a at For last a 26 CO cd 4J afi o C H O r-i X 00 bO C H co fi co QJ 4-1 fi H s CO CM 0) O m 4-1 4-1 < fi H OJ O fi Ph P. o G< H QJ > 13 QJ QJT3 P, O QJ rH 4-> QJ cd > O CU >H TJT3 fi <U -H rH H CO <4H U O QJ U & O fi H QJ rl fi bS rl pH fi 27 resort. In series, four 35 Each tank and the was then was onto consisted seconds. using POTA more mind steel filled wound every 30 no mm in the as than +.04 and placed air and dry. Macbeth TD a developer. given 30-minute wash; All density each are The remaining processing fixer, a 23C. to inverting for any for developing The results the from strips tanks the were of strip solution. for tank tried. solution exposed into the The 5 seconds in Figure 5 for density varied by exposure. included strips measurements 504 Densitometer, Each shown each development time approximately 225ml reel of need Nikor with a the separate temperature adjusted Agitation n=3, to attempt keeping and other an R.I.T. a stop bath, were then allowed were made #113368. on the to 28 m CO rl 0 o l+H bO C rl CO . ^ co OJ CO 4J cu fi 4-1 C 0 rl C fi H fi fi rl o> QJ T3 Fi s rl r-^ 4-1 4-1 C 01 * fi in Pa u o OH <4H 0) > <3 QJ E-ffi O Ph 0) 4-1 fi cd o H r-l 'OTJ 0) fi Pa-rl o co rH QJ U > cu QJ fi S .O QJ S rH H <4H o CO >H^ O fi rl cd s 4-1 m QJ U 2 bO H Pn IV. The of a in the related can be to the Todd cut-off and determined Todd maximum by highlights pictorial problem at points the requisite that states which useful the minimum image range to of in films the ' a the response be of latitude, exposure ficed for the suggested, speed the maximum as the base the point, point purpose minimum and where are that exposure plus Table V. fog. By of any exposure of this useful was needed to A summary exposure repeating the produce of the a was taken was exposure speed a value point density latitudes plotting 29 As Jones research. The measurement established decreased to curve. useful for the precedent criterion a slope for the slope doubt no provides useful the maximum useful the which in shadow and For negatives of the minimum due to lack subject defining is defined by the speed point, the maximum exposure has never been well defined. Therefore, latitude say that the exposures slope exposure contrast respectively. subjects the arises continues latitude exposure been clearly defined never 32 The unacceptable. minimum has "maximum luminance accommodated." exposure comes emulsion literature. is for measuring the criterion photographic DISCUSSION and was of is slope of .1 which suf- 33 at the defined .3x as the defined above given in determination 30 TABLE V Exposure and Gamma as a Function Development Time for the Various Development Formulations Latitude, Speed, No bu Efer Borax of Kodalk Carbonate ' Dev. Dev. Formulation time Lat. Speed 6 time Dev. Lat. Speed 6 time Dev. Lat. Speed 2 160 2.2 .34 2 152 3.16 .60 1 150 2.8 4 180 3.2 .42 3 238 6.0 .65 2 232 5.8 POTA 5 214 4.4 .46 4 198 7.6 .78 3 200 7.2 1.5g/l Phen. 7 230 6.6 .66 5 188 8.3 1.00 4 170 9.1 9 228 7.6 .85 11 194 9.1 1.01 .38 6 time Lat. Speed 6 | - .33 .68 .88 1.13 2 144 6.92 3 178 9.1 4 198 11.6 .80 1.2 2 170 2.4 2 188 5.3 .70 1 162 4.0 .50 1 230 5.5 3 208 4.0 .56 3 212 7.9 .93 2 182 7.2 .92 2 184 7.9 1.0 2.5g/l Phen. 4 218 5.0 .65 4 200 9.1 1.18 3 204 9.1 1.2 3 161 7.2 1.6 5 208 6.0 5 188 11.0 1.38 4 190 10.5 1.4 4 154 12.6 1.8 3 164 1.74 .24 2 116 1.5 .23 2 154 3.2 2 188 5.5 4 162 2.5 .30 3 186 2.8 .31 3 170 5.0 3 224 7.9 1.0 5 208 4.6 .35 4 188 4.4 .40 4 180 6.6 .42 4 130 7.2 1.6 6 204 5.5 .40 5 204 6.0 .50 5 172 7.6 .56 5 146 12.6 1.8 4 166 1.3 .60 3 158 2.6 .69 6 166 1.7 .76 5 170 4.2 .98 7 182 5.8 POTA .5g/l Phen. POTA POTA + H Q 1:1 (1.5g/lPhen.) POTA + H Q 3:1 (1.5g/lPhen.) POTA + 2 204 4.79 3 208 6.30 4 222 7.59 5 182 9.55 2 186 3.63 3 216 4.79 (.5g/lPhen.) D-19 7.2 7.2 1.67 7 176 7.6 1.64 170 6.92 1.46 1 178 6.3 1.13 1 200 7.24 1.17 3 160 9.12 1.70 2 164 10.0 1.70 1.5 160 10.47 1.63 4 138 2.0 3 142 12.6 1.86 2 150 11.48 1.84 4 132 13.8 2.04 2.5 132 11.48 2.0 1.2 .40 .58 .50 .66 .80 218 8.3 1.0 1 118 2.01 2.25 2 104 3.02 2.80 4 102 4.37 2.72 5.50 3.10 94 1.40 2 5 6 6.9 .76 .78 220 176 .60 .70 4 6 166 7.59 6.0 .96 1.40 9 11.0 12.6 1.84 5 146 2 202 6.31 .88 1 192 5.24 3 192 8.32 1.13 2 226 9.12 4 184 10.47 1.30 3 186 5 162 10.96 1.50 4 146 2 3 4 5 196 160 156 142 5.75 7.59 9.12 10.0 1.34 1 192 1 74 15.8 1.0 2 224 14.5 11.48 1.32 4 216 9.6 1.0 12.02 1.6 5 198 6.9 1.3 1.40 6.03 .56 1 156 158 8.7 1.80 9.33 1.80 164 7.94 1.42 1.78 3 132 9.55 2.16 2 145 1.82 4 124 2.45 2.5 124 12.0 .76 1.06 2 1.65 10.0 1 .52 6.3 1.5 1 .50 1.18 6.03 226 5.0 2.8 230 3 3.0 170 2.2 H2Q 1:3 174 168 228 5.5 2 4 164 1.0 ! .58 10 5 196 .30 8 4 2 .25 .58 1.02 2g/l Br. ' i POTA .80 ! .96 2.08 1 31 for five replicates, obtained would the and be considered should but to one method for the Several characteristic A point. was sure to used values curve, varied a the linearly through a then were chosen: In linear as a rate. and 2/3 absolute various method of that similar, derived from at constant which the of set to curvature, in the sum the D-Log density was data the of expo general of slope obtain residual exposure cases, of this Three shoulder Each The greater of minimum the fog plus therefore, line fit. a a the development. program of a 1.3, .5, and at regression measure corresponding to of over time, development of straight used with of altered that were time rate 1.7, addition clarification toe, mid-density, respectively. measure squares determine the varia experiment. require vs. the the use the results measurements curve the of relationship among entire density of plot represented E other by determination and in latitude latitude that was data indicate, Because the base easier +.04 of .08 the produced noted the retained is kept was was speed another. speed measuring exposure be also for method values speeds the the on of As significant. effect It gradient speed difference a in the POTA formula bromide. deviation standard therefore, greatest tions a used was as run least squares higher the deviation from linearity. was number Those 32 plots which after normalization initial gave residual a were development a of development for Microfile Effect of of the increasing a pH did constant not or show the is 1.5 E Log the pH of was used 6 shows the rate in D-19 increase the E POTA. and plus 2 when is the is which The The present pH bromide effect is and of somewhat plus the more hydroquinone the mark pH a and 9 the a pH large the 0.0 curve the on log exposure has represents is the fastest. hydroquinone by slope Phenidone the symbol The indicated 8 symbols which when given when is the square involved. is and before the carbonate, varying of there by symbols curve 10 Figures constant but a through Similarly, . represented 10. for concentration 7. Figure changing the agent either toe. or unaffected In Figure g/1 constant, speed curve, shoulder for the corresponding POTA being developing bromide is held in Figure shifted. between of of D-Log the latitude been is slope factors 2.5 g/1, respectively speed, axis points the softening effect in squares increased the development rate, pH alter concentration shift the processed other concentration g/1 and raised, all significantly or contrast, change and nonlinear Figure rate. 5.0 than greater pH In general, At squares least the as measure of considered than rather slope sum interaction the 33 >H H M CO w Q 4 6 DEVELOPMENT TIME Figure 6: Development D-19 () various rate and of POTA exposure 10 (MIN) Microfile processed in Numbers indicate (A). levels. 34 POTA POTA + 1 g/1 Br cr' POTA (2.5 g/1 Phenidone) 1.0 .8 .6 .4 .2 10 10 11 11 pH Figure 7 : Change in development rate with pH for several Numbers indicate various developer formulations. exposure levels. 35 (C T> 0 0) OJ + e H < 4J En -P Pa O C QJ II fi cn Oa< 0 r-i cu QJ +) *2 co c > Ol-H QJ 4-> T) fi C CO -H V 0 rl fi ** U o -^ m >H Cd T3 QJ > C +1 m cd u 0 co UH co a 0 .} rl U 0 rd ffiMH O ^X + rd +1 QJ U V 10 0 Cu X w rl "-' < -H Eh T> O n Q P4 Tl C P o> < C 0 Eh 0) X! O H P< QJ + 4H || fd II "O QJ O fd 0 .fi OJ Pa *-P 0 < 3 H Eh C <U O -H > Pw fi 0) TJ II -^ QJ QJ H -H H rH (d 0 TJ M -H CO OH iH C T3 C iw -H 0 0 S C/3 <4H QJ 00 fi H Aq.xSuea 36 AiisNaa 37 M II HH fi o H cd 4-) TJ o cd U 4-> fi + QJ O <! fi H O O o Pm II cu T> H <, I rl co QJ OJ 4J U 0 O rfi fiMH 4-1 rl QJ 4-> 4-1 HCO 3 cd C rl o K O o PaMH p-i X w rl cd o .fi 4-1 H + 4J H o o fi + O QJ Ph B< P.H O O Ph QJ > QJ T) Tl OJ > fi U H O co QJ QJ bOT) 4-1 fi-rt fi cd rH C o O C/j .fi QJ }H 0 fcO rl f=H AiiSNaa H e 38 increase in considerable the when pH However, as the once rate trated by Similar Hydroquinone the for results addition to at higher initiating of low the exhaustion exposure, shown regions. This compared more pronounced tion that the as developer of raised effects 1.5 to g/1 and 2, and approximately appear at the hydro for the other rate can carbonate sodium hydroquinone of effects. in the the of can is curves g/1 10, lower are at (.5 g/1) regions be if Figure seen that the supports effect the 12 is observa place. Phenidone negligible which high in those taking with of density fact increases, exhaustion 2.5 illus also Phenidone loss density Variation between tions and of in pH latitude, the is and Concentration extreme Figure with speed of ionization is occurring decrease adding large increase in The superadditive Agent the by on This obtained concentration developer is were increased the Developing At effect borax, Kodalk, of attributed pHs no g/1 concentration concentrations. be Effect 1 a by increased the pH data in Table V. the 9.2 to raised increase in in Figure 11 quinone. had been pH decrease in latitude and buffer capacity increased. the and development but had of indicated with raised any further borax, the was contrast point concentration. concentra the until the pH is exhaustion This is 39 < fiH OON rl pn 4-1 cd T) C II }H 4-1 cd < fi CU o h\" rH - fi CO O O 4-) }-| QJ O MH fi fi QJ fi -rl 4-J o 6 cd QJ c c rl<f 0 O 43 CT"d U O fi cd }H Cd o TJ >^CO + r-<a QJ O 43C4H H O 4-1 Ph X s D \ cd II ^ u n H O O 43 C/j o CU w + X <d 43 H w o o Pa - CO oi 4-J 4-1 O fi H Ph fi & -H m = hJ 3 2 n rH .^5 CO qjC cd gf^g QJ 4-1 0 cdo W c 43 O rl 0 00 . CM AiisNaa M rl C=H rl rH + 6 40 cd4si MrH 4-1 cd CT) QJ O Ofc4 c o + o < CU H CO O Ph 1 T3 H CO QJ II fi 4J QJ < fi C X\ Ph -rl - B QJ CO 43 QJO- 4-1 4-1 0 fi c o rl QJ S -rl 6 <4H OJ in u P3 s 1=1 cd Pari C o o X\^i 42 4-> }H CO r-l X Cd o o cd PH u fi 0 + X w 043 <J rl o o J 4J + EH o g<:pH cd H co 430 X Ph QJ ? II r) _ qjO TJ Pa fi o cd QJ > rH ^ co OJ M QJ 4J Tl i 0 T) QJ CO cd cu e m u o rl C o M 4-1 MH CM QJ rl 0 50 H Ph Aiiswaa 41 in Figure illustrated The major is concentration without tion where The the change shown 14 concentration the effect exhaustion This of occurred approximately the fact that development sure At unaffected Figure 17 . the exhaus reduces rate Phenidone with 15 in the at 2.2. the This curves become indicating low pH, the with is rate a and that the The g/1. increased to cause levels. of substantiated by maximum slope time at high exhaustion of silver with pH density maximum for the in Figure exposure is nonlinear 1.5 with observation density those with by compared sufficiently high because Microfile has as effect increased was and conjunction large a pH Phenidone silver available Figure by of increasing of time levels, occurring, shown hydroquinone of once in Figure rates the high at 14. buffer, Figure 15, a of development had except hydroquinone had development of rate addition development of agent developing in Figure of addition addition when latitude, developing in rate agent Hydroquinone of the exposure developing the increase the additional is concentration upon the increasing of to again The effects. Effect effect affecting levels pH 13. vs. expos - is 16. the curve addition of shape and speed hydroquinone, are as relatively shown in 42 Cfl^-- QJ >un QJ rH cu M+J rH cd g O CN Xi co U QJ ffi II cd 4J o o 0 C + rl s 4-) - 4-1 QJ co fi QJ O 4-1 TJ Cd ro U 0 -rl O fi fi C4H o rl rl QJ Ph 4-J 4-1 cd QJ 3 43 <d" _i cd Cfi 5h fi O 43 QJMH^ }H O Cd o fi4<5<N OrH O Cd "fi || QJ 8 fi o O + Tl CO 0) QJ fi 43 O PhTJ o H Ph fi W fi 43 4-1 rl TJ CO H 3 + _ >rl QJ fi 4-1 0) fi43 fi Ph -rl grH QJ 43 CO bO LO r?PH O O fitoo^H II " P. Or-I QJ rH nJ T) II W > OJ Tl CO QJ CrH O QJ fi 43 O B rl - QJ B T) W3S,'-I cm C co fi QJ Jh cd 43 o 43 O co QJ rl fi t>0 rl rH AIISN3Q 43 E-( 0.5 2.5 1.5 PHENIDONE Figure 14: Change of Numbers CONCENTRATION in development Phenidone 2.5 1.5 0.5 rate concentration indicate exposure a function for 4 pH levels, levels. as 44 1.8 1.4 1.0 0.6 0.2 11 10 PH Figure 15: in development rate as function of pH for [Phenidone]/ [hydroquinone] ratios of o= 1:3 A Both have a 1:1. and Change = hydroquinone concentration =1.0 Numbers indicate exposure levels. g/1. 45 2.2 1.8 1.4 H H CO 52! W P 1.0 4 2 4 DEVELOPMENT TIME Figure 16: in density and maximum slope as a function of development time for processing in POTA + Kodalk + hydroquinone (1:1). Numbers indicate exposure values. Change 46 QJ fi o fi LD rl fiT) CTfi o cd rl Tj<f >> 43 U o O UH U i i QJ O c CM OH r0 1 1 rH rl 1 C Ph 1 ""> QJ 43 rH i' MH O II ^ CO QJ 4-1 CO O 0 fi rl - 4-J CO -rl cd QJ E3 U 4-> fi<|- co c 0 -rlT) o e fi Cd }H C*v co cd rl s fi) >TJ fi CO o 43 Ph 4-1 X H r^ O W o e> o iJ cd rl O MH 4-> Oj fi m l_j 0) -*. B<^ P.H n o o Ph ii rH QJ > II II QJ TJ QJ < > C U rl fi CO QJ toOTJ 0-ri QJ CdrH 43 O UCO QJ rl 00 0 I CM H bO Ph AiisMaa - O 4-1 0 fi -H E= 47 Effect Bromide Ion Concentration of Of had the latitude and concentration exposure the addition levels. 19, A at strainer fairly trast the to is ion development 18 place derivatives and of attempt in the of to shape the D-Log the bromide. derivative Figure shoulder. exposure 1 in note g/1 Figure re- rate in 20, is con does not, This possibility that to excessive restraint greater bromide period. that increase in only decreased the upon effect no in development a as initiation above the scale, as shown in Table V. 23 indicate addition the an had and rate higher The decrease the interesting also upon results at of observation development the pH exposure, contradict effects development times, vs. of concentration and In took density in the toe than in the It Figure levels usual increasing bromide constant levels. exposure directly however, at bromide ion the indicated in Figure 18, bromide is acting at uniform occurring is all As speed. density of that reveals significant decreased and plot investigated, most bromide of losses speed four factors the curve the visualize of E change the Notice begins response curves in were slope that to differences that plotted. that with take curves, on occurs several Figures with 21, 22 the bromide present, the characteristic 48 toO X Pa OH 4-1 r-i 0 Cd 4-1 + rl O ^ WCH rH >-l cd o C O CUT) UH O TJ O H !*h QJ T) US Cd O 5h + -H S C42<rj 5 OhHH 0 43 HIT U mPh U rH rirH || C QJ ^ bO 4J +4 + o<: CH CM - OO W^ O Ph C II QJ rH 4-> Cd fiT> O fi o -1 -d ^ S R QJ fij T) --<t H CO S OJ O 4J CO rl o 43 rl + < Eh o O 0 UH Ph fi Ph H4*J X 43 EH 4-J cd *, w H 1^. o o $ T! || w o ^i w - .J + 4 = C rl H C m CO 4-1 QJ qj CUT) bOT) 4-J -H fi-H 0 B H fi O E a Cd fi rH QJ rl fi toO H XIISN3Q" QJ 0 c OH Jh B 43 i~i CJ CO 00 - co 49 2.2 H r-i CO S3 H Q 6 4 2 0 DEVELOPMENT Figure 19: Density with A= vs. and TIME development without time bromide POTA + Kodalk + 1 g/1 exposure levels. indicate A= for development POTA + Kodalk; Numbers bromide. 50 m o cn H QJ > CU H QJ QJ U X 4-1 4-1 cd QJ TJ H E w o o rl H 43 s o Ph CQ <4H CO O H QJ C > Ph O O OJ H H 4-1 3 O Cd QJ rl rl H EH 4-1 fi fi CO 3 H OJ O o 13 W fi O O P r. QJ OJ CJ S 4-J o co <J > cd u H QJ Tl 4-J fi cd -h rl CO 4-1 rl C QJ 9i -2 S S Pfi OS H QJ > QJ Ifi O P. O CM CU rl 0 toO H Ph aiva 51 adois >X) -<f CM V V o V s 00 0 < H O CM < Ph H 0 ri Vo 4-1 C QJ B Pa 00 O H QJ > QJ TJ 0/ QJ 4-1 J" w < / Ph 3 CO 0 c H E O Ph r~- X tD W O < . O O O hJ rl O MH QJ rl 0 co O P. cu VO * H \ bO O H co > Q> P. v CM \ O * CO CN QJ rl 1 A O _^4. ? m ? LO CM AiiSNaa 00 0 toO < I H rH 52 3.2 2.8 < 2.4 2.0 1.6 w Ph O rJ <co 1.2 .8 1.2 2.8 1.6 0.0 .8 LOG EXPOSURE Figure 22: Slope vs. in D-19. log exposure for 6-minute development .idU'iS <!- 53 CM r O V v V AiisNaa V \J 54 form the of D-19 derivative curve. Additional Research Although by this research, answered. to Among extensive there are some that are two The and/or particles, (2) average or of principle more in the the un how density of probably in may be the of size increase an left mechanisms density of generated was questions many specific growth increase in the an still data of occurring separately combination. (1) amount is the fundamental these differentiate between growth of an result developing number developed of n I or developing between these power data. function density the density of mechanism constant If the is power the developing constant. increases average is monitored during change the with silver explaining the power result of an increase other size average hand, this is size that in remaining if the covering would indicate that decreasing. mechanisms ability to increase the a remains likely the the which is differentiation between these two in to as it development, particle covering as power then grains, On the in covering indication an is primarily the 35 relatively covering increasing density, growth of extensive If predominant. with number be will distinguishing requires power covering the for method two mechanisms development, of course One grains. The may be exposure useful scale of 55 150 ? 100 CM 4-J m bO < o bO 5H 50 DENSITY 2 Figure 24' Mg of silver/ft development in as (O) function of density for D-19 and () POTA. a 56 film Microfile without Covering power loss of data was toe obtained levels for the two development Table VI and development, difference is the certainly is only contrasts obtained that note a the increasing density, finer more In This may in used. part because both bromide the It emulsion. what are results It is also and for D-19 values the to interesting increase image experiments, is with composed of be due to hydroquinone and would "he be useful, obtained H.R. when results negative developer formulations the with that evident high densities. the preliminary obtained were is It in outlined significant, suggesting that at grains not each. power covering is density factor in the difference between small with 24. several less than that for D-19 is power at and systems in Figure plotted POTA covering the while also speed. and developer were emulsion composition, present, therefore, to or to observe film is developed in POTA. Although concentration this factor Microfile effect into of was should with effect no found be POTA. the variation in sulfite in the preliminary experiments, carried over From this solution-physical account. with into the information development can development of concerning the be fully taken 57 TABLE VI Covering Density mg of Ag/ft D-19 2.14 142.5 1.50 2.10 142 1.47 1.47 105 . 5 Power 102 x POTA 1.40 1.28 97.5 1.18 90 1.3 1.08 82 1.3 .54 .50 41 40 1.3 1.3 1.27 58 Lastly, caused on the interesting would have to on due to the restraint of investigate this process. predominant effect development, it what other effects that would bromide be antifogants V. Of the of four factors investigated, the had the concentration general shape bromide had rates, a levels, exposure large which effects low hindered pHs form silver of rate of The curve. effect at and addition all in decreased development given Phenidone the of 5 of decreased and gamma, caused speeds effect Exposure development exhaustion of of pH rate available g/1 developer where at high to until exposure speeds excessive except with exhaustion levels. increas remained un formed at fog decrease. and of however, produced curve, development increased Hydroquinone development latitude was concentration characteristic formation contrast equal increased the contrast. rate the for The Both a Phenidone concentration; changed high the of concentration In general, ing at latitude the upon restraining resulted losses speed effect characteristic predominant in the changes the the of Variation at greatest bromide ion the latitude. exposure few CONCLUSIONS was not increased to silver 59 were and speed decreased such occurred at very an for until extent heavy similar. a given the that exposures. 60 The ability to while first, exposure range high increased maintaining threshold toe factors: (1) obtain sufficient exposure exhaustion bromide during of should the must rate be creating and available be development. (2) other over within enough Secondly, than what latitude result the two developer slow silver. present is the development maintained without levels, of speed exposure of entire extremes; exhaustion to no is avoid at the soluble liberated two FOOTNOTES 1. M. Levy, (1967). 2. "Wide Latitude Photography p & E. c ^^ 11, 46 , A. Shepp and W. Kammerer, "Increased Detectivity Processing," Gamma P. &. & E. 14, 363 (1970). by Low , 3. 4. R. M. Schaffer P. S. & E. , 15, C.E.Mees Process, 5. D.M. Dutton, 317 (1971). and and T. H. James, The Theory of the Photographic 3rd Edition, Macmillan Company, N.Y., 1966. p. 87. T. H.James and G. C. Higgins, Fundamentals Theory, Morgan and Morgan, New York, 1968, 6. Mees 7. Dainty & R. Shaw, 1974, p. 36. 8. Mees 9. Ibid. and and , 10. Dainty 11. A. 9, 12. "Extended Range Oscillography James, James, p. Photographic 4~2~! 74. p. Image p. Science, Academic Press, New York, 75. 76. p. and Shaw, Marriage, p. 36. "How Many Quanta," J. Photographic Science, (1961). 93 J. B. G. C.Farnell and Photographic Emulsion 9, of Chanter, Grains," (161). 73 James, 13. Mees 14. James 15. Mees 16. Ibid. , p. 88. 17. Ibid. , p. 88. 18. Ibid. , p. 88. 19. Ibid. , p. 90. and and and p. Higgins, James, p. 77. p. 24. 88. 61 "The Quantum Sensitivity Photographic Science, J. ' of " , 62 20. Ibid. 21. Mees 22. Ibid. 23. C. E.Ives, 24. T. H.James, The Theory 102. p. , James, and 352. 350. p. , p. Phot . Eng . . 2, 116 (1951). of the Photographic Process, 1977, p. 440. edition, Macmillan Company, 25. Mees and James, 26. T. H. James, 27. Ibid. , p. 417. 28. Ibid. , p. 325. 29. Dainty 30. L. F. Mason, 31. New Holden H. & W. et 1973, 32. 350. p. 45. Photographic Processing Chemistry, 1966, p. 133. Focal York, al., United Company, p. 4th 442. Shaw, and Press, p. p. ' N.Y., Inc., States Patent 3,772,019 to The St. Johnsbury, Vt , November 13, . 3. St.urge, Neblettes Handbook of Photography and 7 th Edition, Van Nostrand Reinhold Company Reprography N.Y. 1977, p. 191. John M. , , 33. Ibid. 34. Mees 35. Ibid. , p. and , p. 191. James, 333. p. 350. ,
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