EP0571616B1 - Photographic developer stabilisation - Google Patents
Photographic developer stabilisation Download PDFInfo
- Publication number
- EP0571616B1 EP0571616B1 EP93901673A EP93901673A EP0571616B1 EP 0571616 B1 EP0571616 B1 EP 0571616B1 EP 93901673 A EP93901673 A EP 93901673A EP 93901673 A EP93901673 A EP 93901673A EP 0571616 B1 EP0571616 B1 EP 0571616B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- developer
- developing agent
- sulphite
- developing
- agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 230000006641 stabilisation Effects 0.000 title 1
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 42
- 239000000243 solution Substances 0.000 claims abstract description 38
- -1 silver halide Chemical class 0.000 claims abstract description 34
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 230000003647 oxidation Effects 0.000 claims abstract description 22
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 22
- 229910052709 silver Inorganic materials 0.000 claims abstract description 15
- 239000004332 silver Substances 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 12
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims abstract description 12
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 11
- 239000001257 hydrogen Substances 0.000 claims abstract description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
- 239000000654 additive Substances 0.000 claims abstract description 7
- 239000012224 working solution Substances 0.000 claims abstract description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 43
- 239000011668 ascorbic acid Substances 0.000 claims description 21
- 229960005070 ascorbic acid Drugs 0.000 claims description 21
- 235000010323 ascorbic acid Nutrition 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 4
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 3
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 claims description 2
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 claims 1
- 230000018109 developmental process Effects 0.000 description 8
- 238000007792 addition Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 235000002566 Capsicum Nutrition 0.000 description 6
- 239000006002 Pepper Substances 0.000 description 6
- 241000722363 Piper Species 0.000 description 6
- 235000016761 Piper aduncum Nutrition 0.000 description 6
- 235000017804 Piper guineense Nutrition 0.000 description 6
- 235000008184 Piper nigrum Nutrition 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 208000015181 infectious disease Diseases 0.000 description 4
- 230000002458 infectious effect Effects 0.000 description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 4
- 239000004296 sodium metabisulphite Substances 0.000 description 4
- 235000010262 sodium metabisulphite Nutrition 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- DSVIHYOAKPVFEH-UHFFFAOYSA-N 4-(hydroxymethyl)-4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)(CO)CN1C1=CC=CC=C1 DSVIHYOAKPVFEH-UHFFFAOYSA-N 0.000 description 2
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002211 L-ascorbic acid Substances 0.000 description 2
- 235000000069 L-ascorbic acid Nutrition 0.000 description 2
- 229940072107 ascorbate Drugs 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 230000003019 stabilising effect Effects 0.000 description 2
- WKCYFSZDBICRKL-UHFFFAOYSA-N 3-(diethylamino)propan-1-ol Chemical compound CCN(CC)CCCO WKCYFSZDBICRKL-UHFFFAOYSA-N 0.000 description 1
- SJSJAWHHGDPBOC-UHFFFAOYSA-N 4,4-dimethyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)(C)CN1C1=CC=CC=C1 SJSJAWHHGDPBOC-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-MVHIGOERSA-N D-ascorbic acid Chemical compound OC[C@@H](O)[C@@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-MVHIGOERSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000005205 dihydroxybenzenes Chemical class 0.000 description 1
- WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 description 1
- 150000002083 enediols Chemical class 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000019275 potassium ascorbate Nutrition 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229940116357 potassium thiocyanate Drugs 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- 235000019187 sodium-L-ascorbate Nutrition 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/30—Developers
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
Definitions
- This invention relates to a method of stabilising photographic silver halide developer solutions and, in particular, to stabilising them against pH changes brought about by aerial oxidation.
- Photographic silver halide developer solutions are usually alkaline and contain a developing agent (which is a reducing agent) which reduces photoexposed silver halide to silver. Inherently therefore developing agents can react with oxygen in the air to become oxidised and thus ineffective for development purposes. Most developing solutions, however, contain considerable amounts of sulphite whose primary purpose is to protect the developing agent against aerial oxidation. This is effective but will not stabilise a developer over long periods of exposure to the air, eg a day or two if there is a significant surface area exposed to air.
- Infectious development can only take place where there is a very low concentration of sulphite ions, equivalent to some 3 to 5 grams anhydrous sodium sulphite per litre. Under such circumstances, the developing agent is very prone to aerial oxidation making the solution unstable. Infectious developers contain a single developing agent, usually hydroquinone or similar dihydroxybenzene compounds. US Patent Specification 3 512 981 describes the use of ascorbic acid or an analogue thereof in such developing solutions to protect them against aerial oxidation ("tray life").
- US Patent 3,865,591 describes developer compositions containing a dihydroxybenzene developing agent, a 3-pyrazolidone developing agent, an ene-diol developing agent including ascorbic acid and sodium or potassium thiocyanate as a silver halide solvent.
- the advantage is said to be that the developer is capable of increasing the exposure index (speed) of the film that is developed.
- US Patent 3,022,168 describes ascorbic acid based developers having a pH of from 8 to 9.
- Example 3 describes such a developer also containing Metol and hydroquinone.
- US Patent 3,938,997 describes developers comprising an iron chelate developer, an ascorbic acid and a third developing agent which are said to form a ternary superadditive combination at pH 6.
- Example 1 it is shown that the activity of the developer becomes less with ageing and ascorbic acid is said to stabilise it. This is clearly a protection against aerial oxidation of the developing agents which are subject thereto.
- the present invention has as its object the solution to problems associated with dihydroxybenzene-containing developer solutions and their pH fluctuations due to aerial oxidation.
- a method of controlling the pH of photographic silver halide developer solutions which contain a dihydroxybenzene developing agent and a secondary developing agent which together form a super-additive combination and an amount of sulphite ions sufficient to protect the developing agents from aerial oxidation by producing in the working solution a concentration of at least 10g/litre (as anhydrous sodium sulphite) wherein there is added to the developer solution a reducing agent which releases hydrogen ions during aerial oxidation of the developer solution and which is different from any developing agent of the superadditive combination.
- the reducing agent which releases hydrogen ions is a compound of the formula: wherein
- the preferred reducing agents are also silver halide developing agents.
- the developer solution contains hydroquinone as the polyhydroxybenzene developing agent.
- the superadditive developing agents for use with the dihydroxybenzene developing agent may be either N-methyl-p-aminophenol or a pyrazolidone, for example 1-phenyl-3-pyrazolidone, 4-hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidone, or 4,4-dimethyl-1-phenyl-3-pyrazolidone.
- the developer preferably contains sulphite in the working strength solution at above 20 g/l, preferably above 25 g/l and more preferanly above 40 g/l (as anhydrous sodium sulphite).
- the present invention also provides silver halide developer composition having a pH above 9 and which is substantially free from a thiosulphate or thiocyanate silver halide solvent, contains a dihydroxybenzene developing agent and a secondary developing agent which together form a super-additive combination and an amount of sulphite ions sufficient to protect the developing agents from aerial oxidation by producing in the working solution a concentration of at least 10g/litre (as anhydrous sodium sulphite) wherein the developer solution contains a reducing agent, different from any developing agent of the super-additive combination, which releases hydrogen ions during aerial oxidation of the developer solution.
- the preferred developers have a pH in the range from 9 to 13, preferably from 10 to 12.
- the developer solutions may be suitable for use in the graphic arts area, especially to obtain very high contrast images with developers which are designed for use with silver halide materials containing an incorporated hydrazide as nucleating agent.
- Such developer solutions may also contain an amine which helps to provide the desired very high contrast as described in European Patent 0 032 456.
- Such materials often form a so-called “pepper fog” which is due to the spontaneous development of unexposed grains.
- the production of "pepper fog” is increased dramatically when the developer is exposed to the air and is often particularly bad in processors where the cross-over from the developer to the fixer is of a long duration.
- This effect is controlled by the method of the present invention, in particular by the action of the ascorbate ion which releases hydrogen ions on oxidation by silver ions or air.
- the pH can be kept constant.
- Ascorbic acid is also a developing agent hence it will not have gross effects on the sensitometry.
- Example 1 was repeated using 100 ml of developer in a 250 ml beaker thus creating a higher surface to volume ratio of 0.44 cm 2 per ml. This time ascorbic acid additions are compared to polyethylene glycol (PEG) or sugar. The results are shown in Table 2 below. Table 2 Addition grams Start pH Day 6 pH Control 10.40 10.21 PEG 80 10.40 11.13 Sucrose 80 10.40 11.12 Ascorbic Acid 2 10.40 11.08 5 10.40 11.03 10 10.40 10.83 20 10.40 10.55 40 10.40 10.28 80 10.40 10.13 160 10.40 10.00
- PEG polyethylene glycol
- Example 3 was repeated using 0, 5, 10, 15, 20 and 40 g/l of ascorbic acid and adjusting the pH of the solution back to that of the control.
- the samples were developed for 30 or 60 seconds at 35°C and then held in the air for 15, 30 or 60 seconds before stopping in 4% acetic acid.
- the samples were developed in 250ml of solution in a 250ml measuring cylinder which was then left exposed to air.
- the processing was repeated after 2, 3, 4 and 7 days. The results are shown below in Table 4 below.
- C means that the sample was clear of pepper fog.
- Example 3 was repeated but in this case the processing was done in an INTERPRO AR10 machine using solutions at 35°C.
- the speed of the processor was adjusted so that the cross-over from the developer to the fixer varied from 10 to 20 to 34 seconds while the development time also increased from 30 to 60 to 102 seconds. These are referred to as fast, medium and slow in Table 5 below.
- Two solutions were used, these were the developer of Example 3 with 0 and then 10 g/l ascorbic acid both at the same pH. Samples were processed on days 1, 2 and 3 and then evaluated for pepper fog. The results are shown in Tables 5 and 6 below.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
- This invention relates to a method of stabilising photographic silver halide developer solutions and, in particular, to stabilising them against pH changes brought about by aerial oxidation.
- Photographic silver halide developer solutions are usually alkaline and contain a developing agent (which is a reducing agent) which reduces photoexposed silver halide to silver. Inherently therefore developing agents can react with oxygen in the air to become oxidised and thus ineffective for development purposes. Most developing solutions, however, contain considerable amounts of sulphite whose primary purpose is to protect the developing agent against aerial oxidation. This is effective but will not stabilise a developer over long periods of exposure to the air, eg a day or two if there is a significant surface area exposed to air.
- Certain developer solutions in the graphic arts area (not widely used now) produce images of extremely high contrast by a process known as "infectious development". Infectious development can only take place where there is a very low concentration of sulphite ions, equivalent to some 3 to 5 grams anhydrous sodium sulphite per litre. Under such circumstances, the developing agent is very prone to aerial oxidation making the solution unstable. Infectious developers contain a single developing agent, usually hydroquinone or similar dihydroxybenzene compounds. US Patent Specification 3 512 981 describes the use of ascorbic acid or an analogue thereof in such developing solutions to protect them against aerial oxidation ("tray life").
- Other developing solutions containing more sulphite do not suffer this extreme instability but nevertheless not only suffer the normal depletion of developing agent under conditions of use when developing an image but also under conditions of standing idle when a small but measurable amount of aerial oxidation occurs. Under conditions of silver halide development the consumption of dihydroxybenzene developing agent causes the pH of the developer to go down. Under conditions of aerial oxidation and in the presence of sulphite ions, however, the pH tends to go up. It is well known, of course, that the activity of a developing agent is dependant on pH and as this rises, the developing agent becomes more active. Variable pH will therefore lead to variable sensitometric results.
- Under typical conditions of normal use any fall in the pH due to silver halide development occurring can be corrected by the normal replenishment which occurs to replace developing agent and other components in response to the volume of material processed. However, the rise in pH caused by aerial oxidation when idle is difficult to deal with especially over long periods of down time, for example, over a weekend.
- Problems therefore arise with developers containing normal levels (ie not infectious development levels) of sulphite due to pH fluctuations caused both by developing activity and by aerial oxidation.
- US Patent 3,865,591 describes developer compositions containing a dihydroxybenzene developing agent, a 3-pyrazolidone developing agent, an ene-diol developing agent including ascorbic acid and sodium or potassium thiocyanate as a silver halide solvent. The advantage is said to be that the developer is capable of increasing the exposure index (speed) of the film that is developed.
- US Patent 3,022,168 describes ascorbic acid based developers having a pH of from 8 to 9. Example 3 describes such a developer also containing Metol and hydroquinone.
- US Patent 3,938,997 describes developers comprising an iron chelate developer, an ascorbic acid and a third developing agent which are said to form a ternary superadditive combination at pH 6. In Example 1 it is shown that the activity of the developer becomes less with ageing and ascorbic acid is said to stabilise it. This is clearly a protection against aerial oxidation of the developing agents which are subject thereto.
- The present invention has as its object the solution to problems associated with dihydroxybenzene-containing developer solutions and their pH fluctuations due to aerial oxidation.
- According to the present invention there is provided a method of controlling the pH of photographic silver halide developer solutions which contain a dihydroxybenzene developing agent and a secondary developing agent which together form a super-additive combination and an amount of sulphite ions sufficient to protect the developing agents from aerial oxidation by producing in the working solution a concentration of at least 10g/litre (as anhydrous sodium sulphite) wherein there is added to the developer solution a reducing agent which releases hydrogen ions during aerial oxidation of the developer solution and which is different from any developing agent of the superadditive combination.
-
- n is 0, 1, 2, 3 or 4 and
- R is -OH or H but is -OH when n=0,
- The preferred reducing agents are also silver halide developing agents. Examples of compounds of formula (I) include (when n=1) 1-ascorbic acid, d-ascorbic acid, isoascorbic acid, and water-soluble salts thereof, eg potassium or sodium ascorbates.
- Preferably the developer solution contains hydroquinone as the polyhydroxybenzene developing agent.
- The superadditive developing agents for use with the dihydroxybenzene developing agent may be either N-methyl-p-aminophenol or a pyrazolidone, for example 1-phenyl-3-pyrazolidone, 4-hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidone, or 4,4-dimethyl-1-phenyl-3-pyrazolidone.
- The developer preferably contains sulphite in the working strength solution at above 20 g/l, preferably above 25 g/l and more preferanly above 40 g/l (as anhydrous sodium sulphite).
- The present invention also provides silver halide developer composition having a pH above 9 and which is substantially free from a thiosulphate or thiocyanate silver halide solvent, contains a dihydroxybenzene developing agent and a secondary developing agent which together form a super-additive combination and an amount of sulphite ions sufficient to protect the developing agents from aerial oxidation by producing in the working solution a concentration of at least 10g/litre (as anhydrous sodium sulphite) wherein the developer solution contains a reducing agent, different from any developing agent of the super-additive combination, which releases hydrogen ions during aerial oxidation of the developer solution.
- The preferred developers have a pH in the range from 9 to 13, preferably from 10 to 12.
- The developer solutions may be suitable for use in the graphic arts area, especially to obtain very high contrast images with developers which are designed for use with silver halide materials containing an incorporated hydrazide as nucleating agent. Such developer solutions may also contain an amine which helps to provide the desired very high contrast as described in European Patent 0 032 456.
- Such materials often form a so-called "pepper fog" which is due to the spontaneous development of unexposed grains. The production of "pepper fog" is increased dramatically when the developer is exposed to the air and is often particularly bad in processors where the cross-over from the developer to the fixer is of a long duration. This effect is controlled by the method of the present invention, in particular by the action of the ascorbate ion which releases hydrogen ions on oxidation by silver ions or air. Thus in a developer which comprises a mixture of hydroquinone and ascorbate ions the pH can be kept constant. Ascorbic acid is also a developing agent hence it will not have gross effects on the sensitometry.
- The following Examples are included for a better understanding of the invention.
- The following basic developer formulation was used:
Sodium sulphite (anhy) 40.0 g/l Sodium bicarbonate (anhy) 20.0 Hydroquinone 18.0 1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone 1.0 Sodium bromide 2.5 5-Methylbenzotriazole 0.15 Potassium Hydroxide to pH=10.3 - 250 ml portions of the developer were placed in 250 ml beakers and the following compounds added at varying levels:
- (a) Sodium metabisulphite
- (b) Sodium sulphate
- (c) Ascorbic acid.
- The pH levels of all the solutions were made equal to the pH of the original solution (pH=10.37). The beakers were then exposed to air for 6 days and the pH levels measured. The resulting pH's are recorded below in Table 1. The surface area per ml was 0.27 cm2.
Table 1 Addition grams Start pH Day 6 pH Sodium Metabisulphite 15 10.37 10.66 30 10.37 10.67 60 10.37 10.68 120 10.37 10.59 240 10.37 10.52 Sodium Sulphate 15 10.37 10.74 30 10.37 10.65 60 10.37 10.63 120 10.37 10.73 240 10.37 10.62 Ascorbic Acid 5 10.37 10.60 10 10.37 10.53 15 10.37 10.47 30 10.37 10.29 60 10.37 10.22 120 10.37 10.06 - The results show that the pH rises with time even with a reducing salt (metabisulphite) while the amount of ascorbic acid controls the degree of rise or fall of the pH.
- Example 1 was repeated using 100 ml of developer in a 250 ml beaker thus creating a higher surface to volume ratio of 0.44 cm2 per ml. This time ascorbic acid additions are compared to polyethylene glycol (PEG) or sugar. The results are shown in Table 2 below.
Table 2 Addition grams Start pH Day 6 pH Control 10.40 10.21 PEG 80 10.40 11.13 Sucrose 80 10.40 11.12 Ascorbic Acid 2 10.40 11.08 5 10.40 11.03 10 10.40 10.83 20 10.40 10.55 40 10.40 10.28 80 10.40 10.13 160 10.40 10.00 - Results similar to Example 1 are obtained but the rise in pH of the comparative solutions is exaggerated by the greater surface to volume ratio.
- A batch of Kodak UGF film was cut into 35mm strips and then developed in the Developer of the formula:
Sodium sulphite (anhy) 75.0 g/l Sodium bicarbonate (anhy) 7.0 Hydroquinone 40.0 1-phenyl-4,4'-diethyl-3-pyrazolidone 0.4 Sodium bromide 3.0 5-Methylbenzotriazole 0.8 Disodium salt of EDTA 1.0 3-diethylamino-1-propanol 45.0 Potassium Hydroxide to pH=11.3 - The strips were developed for 30 seconds or 60 seconds and then held in the air to simulate long "cross-overs". They were then placed in a stop bath of 4% acetic acid and then fixed in Kodak Fixer 3000 (1+3). The developed strips were examined for the presence of "pepper fog" and rated on a scale of 1-10 (10 worst). The results are shown in Table 3 below.
Table 3 Addition g/l 60 sec 30 sec Ascorbic Acid 0 10 9-10 5 9 9 10 3-4 3-4 15 2 2 20 <2 <2 30 <2 <2 40 <2 <2 Sodium metabisulphite 10 >10 >10 20 >10 >10 40 >10 >10 - The results show that fresh developer with a level of 5g/l of ascorbic acid reduces the defect and that 15 g/l eliminates the problem.
- Example 3 was repeated using 0, 5, 10, 15, 20 and 40 g/l of ascorbic acid and adjusting the pH of the solution back to that of the control. The samples were developed for 30 or 60 seconds at 35°C and then held in the air for 15, 30 or 60 seconds before stopping in 4% acetic acid. The samples were developed in 250ml of solution in a 250ml measuring cylinder which was then left exposed to air. The processing was repeated after 2, 3, 4 and 7 days. The results are shown below in Table 4 below. C means that the sample was clear of pepper fog.
Table 4 DEV/AIR (secs) Day 1 Day 2 Day 3 Day 4 Day 5 C 10 g 60/60 C <2 <2 <2 C 60/30 <2 <2 <2 <2 C 60/15 <2 <2 <2 <2 C 30/60 <2 C C C C 30/30 C C C C C 30/15 C C C C C 5 g 60/60 6 7 7 7.5 <2 60/30 6 6 6 6 <2 60/15 3.5 6 5 6 C 30/60 <2 2-3 <2 <2 C 30/30 <2 <2 <2 <2 <2 30/15 <2 <2 <2 <2 <2 0 g 60/60 9 8 9 9 2 60/30 8 8 8 9 2 60/15 8 7.5 8 8.5 <2 30/60 6 6 6.5 6 C 30/30 7 4 6 6 C 30/15 <2 4 5 6 C - The results show that a level of 10g/l of ascorbic acid was sufficient to overcome the defect under all the conditions used. The control's improvement after 7 days is due to the decreased level of developing agent caused by the excessive amount of aerial oxidation.
- Example 3 was repeated but in this case the processing was done in an INTERPRO AR10 machine using solutions at 35°C. The speed of the processor was adjusted so that the cross-over from the developer to the fixer varied from 10 to 20 to 34 seconds while the development time also increased from 30 to 60 to 102 seconds. These are referred to as fast, medium and slow in Table 5 below. Two solutions were used, these were the developer of Example 3 with 0 and then 10 g/l ascorbic acid both at the same pH. Samples were processed on days 1, 2 and 3 and then evaluated for pepper fog. The results are shown in Tables 5 and 6 below.
Table 5 - Control Developer Speed Day 1 Day 2 Day 3 Slow 5 7 8 Slow 5 7 8 Medium 5 4 4 Medium 5 4 4 Fast <2 2 2 Fast <2 2 2 Table 6 - 10 g/l Ascorbic Acid added Speed Day 1 Day 2 Day 3 Slow C <2 3-4 Slow C <2 3-4 Medium C C C Medium C C C Fast C C C Fast C C C - The results again show that the pepper fog formed in the control solution is overcome by the addition of ascorbic acid.
Claims (10)
- A method of controlling the pH of photographic silver halide developer solutions which contain a dihydroxybenzene developing agent and a secondary developing agent which together form a super-additive combination and an amount of sulphite ions sufficient to protect the developing agents from aerial oxidation by producing in the working solution a concentration of at least 10g/litre (as anhydrous sodium sulphite) wherein there is added to the developer solution a reducing agent which releases hydrogen ions during aerial oxidation of the developer solution and which is different from any developing agent of the superadditive combination.
- A method as claimed in claim 1 or 2 in which the reducing agent which releases hydrogen ions is ascorbic acid.
- A method as claimed in any of claims 1 to 3 in which the dihydroxybenzene developing agent is hydroquinone.
- A method as claimed in any of claims 1 to 4 in which the pH of the developer solution is from 9 to 13, preferably from 10 to 12.
- A method in which the superadditive combination comprises hydroquinone and either N-methyl-p-aminophenol or a pyrazolidone.
- A method as claimed in any of claims 1 to 6 in which the working strength developer solution comprises at least 25 g/l, preferably 40 g/l, of sulphite (as anhydrous sodium sulphite).
- A silver halide developer composition having a pH above 9 and which is substantially free from a thiosulphate or thiocyanate silver halide solvent, contains a dihydroxybenzene developing agent and a secondary developing agent which together form a super-additive combination and an amount of sulphite ions sufficient to protect the developing agents from aerial oxidation by producing in the working solution a concentration of at least 10g/litre (as anhydrous sodium sulphite) wherein the developer solution contains a reducing agent, different from any developing agent of the super-additive combination, which releases hydrogen ions during aerial oxidation of the developer solution.
- A developer composition as claimed in claim 8 in which the reducing agent is a compound as claimed in claim 2 or 3.
- A developer as claimed in claim 8 or 9 having a composition as defined in any of claims 4 to 7.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB919126362A GB9126362D0 (en) | 1991-12-12 | 1991-12-12 | Photographic developer stabilisation |
GB9126362 | 1991-12-12 | ||
PCT/EP1992/002849 WO1993012463A1 (en) | 1991-12-12 | 1992-12-10 | Photographic developer stabilisation |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0571616A1 EP0571616A1 (en) | 1993-12-01 |
EP0571616B1 true EP0571616B1 (en) | 1997-09-10 |
Family
ID=10706113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP93901673A Expired - Lifetime EP0571616B1 (en) | 1991-12-12 | 1992-12-10 | Photographic developer stabilisation |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0571616B1 (en) |
JP (1) | JP3249521B2 (en) |
DE (1) | DE69222153T2 (en) |
GB (1) | GB9126362D0 (en) |
WO (1) | WO1993012463A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06308679A (en) * | 1993-04-27 | 1994-11-04 | Fuji Photo Film Co Ltd | Method for processing silver photographic sensitive material |
JP3148467B2 (en) * | 1993-06-18 | 2001-03-19 | 富士写真フイルム株式会社 | Image forming method |
EP0732619A1 (en) * | 1995-02-21 | 1996-09-18 | Agfa-Gevaert N.V. | Developing method and method for developing an exposed photographic silver halide material |
US6379877B1 (en) | 1995-02-21 | 2002-04-30 | Agfa-Gevaert | Method for developing an exposed photographic silver halide material |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3022168A (en) * | 1958-06-28 | 1962-02-20 | Pharmacia Ab | Photographic developer |
US3867151A (en) * | 1973-05-10 | 1975-02-18 | Delaware Photographic Products | General purpose monobath |
US3865591A (en) * | 1973-05-10 | 1975-02-11 | Delaware Photographic Products | General purpose developer |
-
1991
- 1991-12-12 GB GB919126362A patent/GB9126362D0/en active Pending
-
1992
- 1992-12-10 DE DE69222153T patent/DE69222153T2/en not_active Expired - Fee Related
- 1992-12-10 WO PCT/EP1992/002849 patent/WO1993012463A1/en active IP Right Grant
- 1992-12-10 JP JP51060093A patent/JP3249521B2/en not_active Expired - Fee Related
- 1992-12-10 EP EP93901673A patent/EP0571616B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP3249521B2 (en) | 2002-01-21 |
DE69222153T2 (en) | 1998-04-09 |
GB9126362D0 (en) | 1992-02-12 |
WO1993012463A1 (en) | 1993-06-24 |
EP0571616A1 (en) | 1993-12-01 |
DE69222153D1 (en) | 1997-10-16 |
JPH06508226A (en) | 1994-09-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0461783B1 (en) | Photographic developer composition | |
JPH04270343A (en) | Developer composition for photography | |
EP0724193B1 (en) | Radiographic film developers containing ascorbic acid and thioether development accelerators | |
EP0573700A1 (en) | Replenishment of a developer containing ascorbic acid and 3-pyrazolidone derivatives | |
EP0603586A1 (en) | Photographic developing solution | |
CA1060697A (en) | Processing solution for use as photographic developer bath and replenisher therefor | |
AU689168C (en) | Non-hydroquinone photographic developer composition and processing method | |
CA1110483A (en) | High contrast continuous tone developer containing hydroquinone, sulfite, organic azole antifogging agent and alkanolamine | |
EP0571616B1 (en) | Photographic developer stabilisation | |
EP0071344B1 (en) | Stable photographic developer and replenisher therefor | |
EP0136582B1 (en) | Developer compositions for silver halide photographic materials | |
US3512981A (en) | Stable photographic developers containing ascorbic acid | |
US5147767A (en) | Gluconic acid-based developer composition | |
EP0446457B1 (en) | Alkaline black-and-white photographic developer | |
EP0666501A2 (en) | Hardening developer for silver halide photography and development method | |
US5108880A (en) | Developer composition for silver halide photographic material | |
EP1231504B1 (en) | Photographic developing composition and use thereof in the development of a photographic element | |
WO1996003677A1 (en) | Photographic developing composition and its application | |
US3772022A (en) | Developing composition for use with photographic materials for the graphic arts | |
JP3030589B2 (en) | Processing agents for black and white silver halide photographic materials, developers for black and white silver halide photographic materials and fixing agents for silver halide photographic materials | |
EP0239149B1 (en) | High contrast development of silver halide emulsion material | |
JP3243669B2 (en) | Single solid fixative | |
EP0736802A1 (en) | Photographic silver halide developer composition and method | |
JPS58174948A (en) | Replenisher for development | |
JP2002156732A (en) | Processing method for silver halide photographic sensitive material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19930811 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): CH DE FR GB IT LI |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
17Q | First examination report despatched |
Effective date: 19961118 |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
RBV | Designated contracting states (corrected) |
Designated state(s): DE FR GB |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: EASTMAN KODAK COMPANY Owner name: KODAK LIMITED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR GB |
|
REF | Corresponds to: |
Ref document number: 69222153 Country of ref document: DE Date of ref document: 19971016 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19981110 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19981203 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19981230 Year of fee payment: 7 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19991210 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19991210 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20000831 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20001003 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |