US3712818A - Photographic stabilising or fixing bath - Google Patents
Photographic stabilising or fixing bath Download PDFInfo
- Publication number
- US3712818A US3712818A US00836661A US3712818DA US3712818A US 3712818 A US3712818 A US 3712818A US 00836661 A US00836661 A US 00836661A US 3712818D A US3712818D A US 3712818DA US 3712818 A US3712818 A US 3712818A
- Authority
- US
- United States
- Prior art keywords
- bath
- fixing
- stabilising
- photographic
- baths
- 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
- 230000003019 stabilising effect Effects 0.000 title description 15
- -1 SILVER HALIDE Chemical class 0.000 abstract description 24
- 229910052709 silver Inorganic materials 0.000 abstract description 20
- 239000004332 silver Substances 0.000 abstract description 20
- 239000003381 stabilizer Substances 0.000 abstract description 18
- 239000000839 emulsion Substances 0.000 abstract description 17
- 230000006641 stabilisation Effects 0.000 abstract description 9
- HAZJTCQWIDBCCE-UHFFFAOYSA-N 1h-triazine-6-thione Chemical compound SC1=CC=NN=N1 HAZJTCQWIDBCCE-UHFFFAOYSA-N 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 150000003918 triazines Chemical class 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000005352 clarification Methods 0.000 description 5
- 229940125898 compound 5 Drugs 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 5
- 235000019345 sodium thiosulphate Nutrition 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 239000001828 Gelatine Substances 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 238000004061 bleaching Methods 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 238000003672 processing method Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003567 thiocyanates Chemical class 0.000 description 2
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910052946 acanthite Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229940100890 silver compound Drugs 0.000 description 1
- 150000003379 silver compounds Chemical class 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- XUARKZBEFFVFRG-UHFFFAOYSA-N silver sulfide Chemical compound [S-2].[Ag+].[Ag+] XUARKZBEFFVFRG-UHFFFAOYSA-N 0.000 description 1
- 229940056910 silver sulfide Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 238000004383 yellowing Methods 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
- G03C5/38—Fixing; Developing-fixing; Hardening-fixing
Definitions
- the invention relates to a bath for stabilising or fixing exposed and developed photographic silver halide emulsion layers, which contains mercaptotriazine compounds as stabilising or fixing compounds.
- stabilisation is intended to mean the conversion of the remaining light sensitive silver halide which is present in an exposed and developed silver halide emulsion layer into a complex silver compound which is not light sensitive.
- This silver complex may either remain in the layer or may be partly or completely Washed out.
- Fixing is intended to mean dissolving the light sensitive silver halide out of the developed silver halide emulsion layer. Both methods serve the same purpose, namely to render the layer which carries the final photographic image insensitive to light. However, any transitional stage between these two extreme cases in which either all the light insensitive complex remains in the layer or is completely removed by dissolving out soluble complexes from the layer is possible. This depends mainly on the Water solubility of the complex and on the treatment time in the stabilising bath or on the length of time for which the material is subsequently washed.
- Stabilisation of a developed silver halide emulsion layer generally proceeds much more rapidly than conventional fixing, so that this method of working is particularly important for modern high speed processing methods.
- stabilising agents are already known, they do not meet all the practical requirements.
- One of the most serious disadvantages is the gradual discolouration, especially of the white parts of the finished silver image which may become yellow to deep brown. This eifect is due to an insufiicient stability of the silver complex. Free silver ions are formed and these cause the discoloration.
- Another serious disadvantage is bleaching of the silver image.
- Other known stabilizing agents such as thiocyanates are strongly hygroscopic. The resulting high moisture content often leads to sticky layers.
- Other stabilizing agents are not sufficiently effective or can be used only at relatively high pH values which cannot be tolerated in photographic layers.
- Thiourea and similar compounds are only stable at acid pH values. They are decomposed in alkaline mediums to yield silver sulfide. Many of the heterocyclic mercapto compounds described for this purpose cause fogging of the photographic layer in the developer baths. This is a serious disadvantage since it is almost impossible to avoid contamination of the developer bath with small quantities of the stabilising bath
- R or R is a hydrogen atom, a saturated or unsaturated aliphatic group having up to 6 carbon atoms such as methyl, ethyl propyl, butyl or allyl groups which may be substituted, e.g. with phenyl groups as in the benzyl or phenylethyl radicals or an aryl radical, in particular a phenyl group;
- R is a hydrogen atom, a saturated or unsaturated aliphatic group having up to 6 carbon atoms such as methyl, ethyl, butyl or allyl groups, which aliphatic groups may be substituted with hydroxyl, alkoxy, amino halogen or phenyl groups such as hydroxymethyl, 2- hydroxypropyl, 2 -methoxyethy1, '2 aminoethyl, 3-dimethylaminopropyl, 2-chloroethyl or 3-chloropropyl or benzyl group or is an aryl group, in particular a phenyl group.
- the solubility of the compounds can be influenced as desired by suitable choice of the substituents R, R and o R" and the compounds can thus be adapted to the par ticular purpose for which they are to be used.
- the compounds which are used according to the invention can be prepared by known processes, for example as described by Dixon, J. Chem. Soc. (London) 61, 510, Burke, J. Am. Chem. Soc. 69, 236-237 (1947) or Paquin, Angew. Chem. 60, 267 (194-8).
- the method of preparation of compounds and 7 is described in detail below.
- COMPOUND 5 70 g. of ethanolamine is introduced into a mixture of 76 g. of thiourea and 60 g. of paraformaldehyde in 250 ml. of isopropanol in such a way, with stirring and cooling, that the temperature does not exceed C. The mixture is then heated under reflux for 2 hours, cooled, filtered with suction and washed with isopropanol. Yield 132 g. When recrystallised from methanol, the compound melts at 163-165" C.
- COMPOUND 7 160 ml. of a Formalin solution is introduced with stirring to a mixture of 102 g. of 1-amino-3-dimethylamino propane and 76 g. of thiourea in the course of 20 minutes, the temperature rising to 85 C. in the process. The reaction mixture is then heated for 10 minutes at 90 C., and after cooling, suction filtration, Washing with isopropanol and drying, 110 g. of compound 7 of M.P. 145-147" C. are obtained. After recrystallisation from methanol, the substance melts at 148 C.
- Tihfl baths according to the invention can be used both as stabilising baths and as fixing baths. Whether they are used for one or the other purpose depends on the watersolubility of the complex compounds formed between the silver halide and the triazine compounds contained in the baths and, of course, on the length of the treatment time of the developed photographic material in the bath and the length of any subsequent washing.
- the required fixing times are much shorter than for the conventional sodium thiosulfate fixing baths. If elevated temperatures are employed, as is the case with high speed processing methods, e.g. temperatures of about 50 C., the fixing times are only slightly longer than in ammonium thiosulfate baths. It is also advantageous that the baths prepared according to the invention may have an acid pH as is required e.g. for short stop fixing baths, since the triazine compounds are stable at pH values between 1 and 4. Thiosulfate fixing baths, on the other hand, must not be allowed to have pH values below 4 because decomposition of the thiosulfate then occurs.
- the baths according to the invention are particularly advantageous if they are used as stabilising baths, especially in high speed processing methods.
- the stabilising time is very short, 30 seconds to 3 minutes generally being sulficient.
- the photographic images which have been stabilised with the baths prepared according to the invention show practically no discoloration even after prolonged storage.
- the finished silver image is very stable even Without the presence of stabilisers such as phenylmercaptotetrazole which are usually added, and bleaching occurs only to a very small extent even after prolonged storage under tropical conditions.
- the baths may have either an acid or an alkaline pH when they are used as stabiliser or fixer baths. In this respect they are far superior to the usual stabiliser baths which contain thiocyanates or thiourea.
- the stabiliser baths according to the invention should preferably have a slightly acid pH value of about 4 to 6.5.
- the triazine compounds contained in the baths according to the invention are photographically inert. Fogging of the photographic layers does not occur even if traces of the compounds enter the developer bath.
- the amount of triazine compounds contained in the baths according to the invention may vary within wide limits. Quantities of between 50 and 250 g. per litre are generally suflicient. The optimum concentrations for any particular process can be easily determined by simple small scale tests.
- the baths according to the invention are prepared by simply dissolving the triazine compounds in water.
- a small quantity of a water-soluble solvent such as formamide, dimethylformamide etc. is preferably added to the baths according to the invention. This results in an improvement of the diffusion into the gelatine layers.
- the mercaptotriazines are particularly useful in very viscous high speed fixing baths. Such baths are of great importance in modern high speed processing methods. If known fixing agents, such as ammonium thiosulfate are used, it is extremely difiicult to prepare sufficiently viscous fixing baths of a pasty consistency because at the high thiosulfate concentrations required, it is not possible to achieve a sufficiently high viscosity with the thickness customarily employed such as cellulose derivatives, e.g. hydroxyethylcellulose.
- the fixing baths according to the invention can be easily adjusted to the required viscosity with the usual thickening agents.
- EXAMPLE 1 Commercial photographic black-white materials containing silver bromide gelatine emulsion layers are exposed behind a step wedge and developed in a hydro- ,quinone/p-aminophenol developer.
- the film samples have the following sensitivities:
- a criterion for determining the completeness of stabilisation is, as in the case of fixing, the clarity of the imagefree parts of the developed and treated photographic material.
- the material to be treated can be stabilised by dipping it in the stabilising baths. It is not necessary, however, to wait until the 'film which is to be stabilised becomes clear in this bath.
- the films may also be treated for only a relatively short time in the bath and then taken out. The stabilising process then continues even after removal from the bath in the developed silver halide emulsion layer which is soaked with stabilising agent.
- the treatment time in the bath is called the immersion time and the time outside the bath is termed the clarification time.
- the efiiciency of the baths according to the invention is clear from the following table.
- the layers which have been stabilised according to the invention are completely non-sticky. Tests on the stabilised pictures after being in the heating cupboard (3 days storage at 46 C.) and under tropical conditions (3 days storage at 60 C; and 50% relative humidity) demonstrate the excellent stability of the stabilised pictures. No discolouration or bleaching occurs.
- EXAMPLE 2 A commercial photographic black-white material con taining a silver iodobromide gelatine emulsion layer is exposed, and two exposed samples are then processed with the following fixing developer's (monobath-processing).
- Fixing developer I G. Hydroquinone 35 l-phenyl-pyrazolidone 7 Sodium sulfite 25 Sodium hydroxide 20 Sodium thiosulfate 150 Made up to 1 litre with water.
- Fixing developer II G. Hydroquinone 35 l-phenyl-pyrazolidone 7 Sodium sulfite 25 Sodium hydroxide 20 Sodium thiosulfate 150 Made up to 1 litre with water.
- Fixing developer II
- the fixing developer was adjusted to pH 12.8 with NaOH.
- the exposed film samples are treated with the above baths for one minute at 20 C.
- the sample strip treated with bath 1 remains cloudy; it is insufiiciently fixed.
- EXAMPLE 3 15 g. of hydroquinone and 7.5 g. of formaldehyde sodium bisulfite are added to 1 kg. of a photographic emulsion which contains 120 g. of gelatine and 0.24 mol of AgCl. The emulsion is applied on baryta paper.
- the rate of processing can be so adjusted that a photographic sheet measuring 30 x 40 cm. takes 60 to seconds to run through the apparatus. If compound 5 in the stabilising bath is replaced by equivalent quantities of other mercapto triazines of dthe above table, the stabilisation times are of the same or er.
- ammonium thiocyanate is used as stabilising agent, similar lengths of time are required. The pictures obtained, however, are unusable owing to their stickiness, especially if materials with a hydrophobic support are used. If other stabilising agents such as thiourea are used instead of the stabilising agents according to the invention, the final picture becomes bleached or discoloured. Suitable tests on photographic. images after storage in the heating cupboard and tropical cupboard show that those which have been processed with the baths according to the invention show excellent stability.
- the stabilizer baths according to the invention are completely harmless physiologically. They are not found to have any unpleasant odour.
- EXAMPLE 4 Samples of the photographic film types described in Example 1 are exposed and developed in a similar manner. However, the samples are not stabilised but fixed. The treatment differs from that described in Example 1 in that the developed film samples are left in the fixing bath until the image-free areas are clear. The optical clarity of these areas is a criterion for the fact that the light sensitive silver halides have been quantitatively dissolved out by the fixing process.
- the film samples are processed in the following baths:
- Bath 1 G. Sodium thiosulfate cryst. 160 Potassium metabisulfite 15 Up to 1000 ml. pH 4.6.
- Bath 2 15% aqueous solution of ammonium thiosulfate
- Bath 4 10% aqueous solution of compound 5, pH 9.5
- Bath 2 is superior to the bath according to the invention in the clarification times, it has the disadvantage for practical purposes of having to be followed by a very long washing to remove excess ammonium thiosulphate quantitatively from the processed layer. This is necessary in the case of ammonium thiosulfate in order to prevent yellowing and bleaching of the finished image.
- the triazine derivatives used in accordance with the invention do not have this disadvantage so that a short washing is suflicient.
- R, or R is a hydrogen atom, or a saturated or unsaturated aliphatic group having up to 6 carbon atoms or a phenyl group;
- R" is an aliphatic group having up to 6 carbon atoms which is substituted with hydroxy, alkoxy, amino, halogen, a CI-I CH 2-thiohexahydro-s-triazinyl group, treating the developed emulsion in the absence of sufficient thiocyanate ions or thiosulfate ions to provide stabilisation, said agent being present in the bath in an amount ranging from 50 g. to 250 g. per liter of the bath whereupon the exposed light-sensitive silver halide is stabilised or removed.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681772734 DE1772734A1 (de) | 1968-06-27 | 1968-06-27 | Photographisches Stabilisier- oder Fixierbad |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3712818A true US3712818A (en) | 1973-01-23 |
Family
ID=5701374
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00836661A Expired - Lifetime US3712818A (en) | 1968-06-27 | 1969-06-25 | Photographic stabilising or fixing bath |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3712818A (enrdf_load_stackoverflow) |
| BE (1) | BE734662A (enrdf_load_stackoverflow) |
| DE (1) | DE1772734A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2014345A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1265886A (enrdf_load_stackoverflow) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3961958A (en) * | 1973-10-18 | 1976-06-08 | Ciba-Geigy Ag | Process for fixing photographic material |
| US4256826A (en) * | 1978-08-14 | 1981-03-17 | Eastman Kodak Company | Bleach-fix sheets |
| US4454216A (en) * | 1981-06-23 | 1984-06-12 | Mitsubishi Paper Mills, Ltd. | Method for making improved lithographic printing plate |
| US4886737A (en) * | 1987-10-02 | 1989-12-12 | Agfa-Gevaert Aktiengesellschaft | Stabilization of a photographically produced silver image |
| EP0500045A1 (en) * | 1991-02-19 | 1992-08-26 | Fuji Photo Film Co., Ltd. | Process of processing silver halide photographic material and photographic processing composition having a fixing ability |
| JP2867350B2 (ja) | 1991-09-19 | 1999-03-08 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
-
1968
- 1968-06-27 DE DE19681772734 patent/DE1772734A1/de active Pending
-
1969
- 1969-06-17 BE BE734662D patent/BE734662A/xx unknown
- 1969-06-24 GB GB1265886D patent/GB1265886A/en not_active Expired
- 1969-06-25 US US00836661A patent/US3712818A/en not_active Expired - Lifetime
- 1969-06-27 FR FR6921787A patent/FR2014345A1/fr not_active Withdrawn
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3961958A (en) * | 1973-10-18 | 1976-06-08 | Ciba-Geigy Ag | Process for fixing photographic material |
| US4256826A (en) * | 1978-08-14 | 1981-03-17 | Eastman Kodak Company | Bleach-fix sheets |
| US4454216A (en) * | 1981-06-23 | 1984-06-12 | Mitsubishi Paper Mills, Ltd. | Method for making improved lithographic printing plate |
| US4886737A (en) * | 1987-10-02 | 1989-12-12 | Agfa-Gevaert Aktiengesellschaft | Stabilization of a photographically produced silver image |
| JP2634646B2 (ja) | 1987-10-02 | 1997-07-30 | アグフア−ゲヴエルト・アクチエンゲゼルシヤフト | 銀塩写真像の安定化方法 |
| EP0500045A1 (en) * | 1991-02-19 | 1992-08-26 | Fuji Photo Film Co., Ltd. | Process of processing silver halide photographic material and photographic processing composition having a fixing ability |
| JP2867350B2 (ja) | 1991-09-19 | 1999-03-08 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2014345A1 (enrdf_load_stackoverflow) | 1970-04-17 |
| GB1265886A (enrdf_load_stackoverflow) | 1972-03-08 |
| DE1772734A1 (de) | 1970-05-14 |
| BE734662A (enrdf_load_stackoverflow) | 1969-12-17 |
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