US3532498A - Photographic developer compositions - Google Patents
Photographic developer compositions Download PDFInfo
- Publication number
- US3532498A US3532498A US583099A US3532498DA US3532498A US 3532498 A US3532498 A US 3532498A US 583099 A US583099 A US 583099A US 3532498D A US3532498D A US 3532498DA US 3532498 A US3532498 A US 3532498A
- Authority
- US
- United States
- Prior art keywords
- solution
- pyrazolidone
- phenyl
- developer
- concentrate
- 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
- 239000000203 mixture Substances 0.000 title description 25
- 239000000243 solution Substances 0.000 description 52
- 235000008504 concentrate Nutrition 0.000 description 37
- 239000012141 concentrate Substances 0.000 description 37
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 14
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 12
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 239000004310 lactic acid Substances 0.000 description 7
- 235000014655 lactic acid Nutrition 0.000 description 7
- 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 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 6
- 239000003513 alkali Substances 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 150000001340 alkali metals Chemical class 0.000 description 6
- 229930188620 butyrolactone Natural products 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 229910052700 potassium Inorganic materials 0.000 description 6
- 239000011591 potassium Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- -1 cyclic ester Chemical class 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 229940116333 ethyl lactate Drugs 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 239000003352 sequestering agent Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000006172 buffering agent Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000011356 non-aqueous organic solvent Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 239000012224 working solution Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- CNYGLHUWJISQMU-UHFFFAOYSA-N n-[2-(ethylamino)ethyl]hydroxylamine Chemical compound CCNCCNO CNYGLHUWJISQMU-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 239000004296 sodium metabisulphite Substances 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- XWNXEWLCHSLQOI-UHFFFAOYSA-K trisodium;triacetate Chemical compound [Na+].[Na+].[Na+].CC([O-])=O.CC([O-])=O.CC([O-])=O XWNXEWLCHSLQOI-UHFFFAOYSA-K 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
- G03C5/264—Supplying of photographic processing chemicals; Preparation or packaging thereof
- G03C5/266—Supplying of photographic processing chemicals; Preparation or packaging thereof of solutions or concentrates
Definitions
- the storage stability of photographic developer compositions is improved by providing a first concentrate containing 1-phenyl-3-pyrazolidone as developing agent which is in the form of a solution in a mixture of (a) butyrolactone or ethyl lactate with (b) formic acid or lactic acid and a second concentrate in the form of a solution of a polyhydric phenol as secondary developer, an alkali, an inorganic sulphite, and an antifoggant.
- the two concentrates are mixed prior to use and the mixture is diluted with water to produce a working strength developer solution having a pH of at least 9.5.
- This invention relates to photographic developer compositions. It is known that photographic developer solutions containing the developing agent 1-phenyl-3-p-yrazolidone in aqueous solutions at a pH of 9.5 or above (i.e. at the pH value at which they are used) at temperatures above 20 C., deteriorate rapidly, as do also aqueous concentrates of 1-phenyl-3-pyrazolidone intended for incorporation into such developer solutions. This deterioration, particularly of aqueous 1-phenyl-3-pyrazolidone-containing concentrates, results in substantial storage problems under commercial conditions, in which it is often desirable to be able to store material for periods up to several years at temperatures which may range as high as 50 to 55 C. This problem is particularly acute in tropical countries.
- Such solutions may be used as storagestable concentrates which can be added to an aqueous bath containing the other ingredients normally present in a 1-phenyl-3-pyrazolidone-containig photographic developing composition, if necessary with further dilution with water, to give a developer solution ready for use.
- the aforementioned other ingredients are ordinarily a polyhydric phenol as secondary developer, an alkali, an inorganic sulphite, an autifoggant, and, optionally, a sequestering agent to prevent precipitation of metal ions in the working solution and a buffering agent.
- one or more of these other ingredients may be dissolved in the 1-phenyl-3-pyrazolidone-containing concentrate.
- the two solutions are supplied in the form of two packs and frequently the quantity of workingstrength developer solution which is required is less than that obtained by the dilution to working-strength of the total contents of the packs.
- the operator is thus faced with the alternatives of (a) diluting the total contents of the packs, either immediately before or after the two concentrates are mixed, thus producing a quantity in excess of his immediate requirements of working-strength developer solution liable to rapid deterioration or (b) taking aliquot portions of solution from the two packs, an operation which frequently requires the very accurate measurement of small volumes of solution.
- photographic developer compositions which take the form of two separate liquid concentrates, of which the first concentrate comprises a solution of l-phenyl-3- pyrazolidone dissolved in a substantially non-aqueous, i.e. containing not more than 5% w./v. of water, solvent in which the 1-phenyl-3-pyrazolidone is at least 5% w./v. soluble and preferably at least 10% W./v. soluble, at 20 C., which is a mixture of two -components, the first component being a water-miscible non-acidic organic solvent such as an ester or a cyclic ester i.e.
- the second concentrate comprises a conventional developer concentrate of the 1-phenyl-3-pyrazolidone-containing type from which the 1-phenyl-3- pyrazolidone has been omitted, the compositions of the two concentrates being such that, on mixing with the second solution enough of the first solution to provide an appropriate proportion of 1-phenyl-3-pyrazolidone (e.g. between 0.1 gram and 2.0 grams per litre of lphenyl-3-pyrazolidone in working-strength developer solutions), the working-strength developer solution obtained by dilution of the mixture with further quantities of water has a pH of 9.5 or above.
- the proportions by volume of the non-acidic organic component and the organic acid component of the solvent of the first solution are within the range 1:1 to 4:1 inclusive.
- the solvent of the first solution must be readily and completely miscible with water at the temperature at which the two solutions are mixed, which will generally be within the range of 20 C. to 30 C.
- the two components of the solvent of the first solution must be substantially non-toxic, free from other serious hazards and suitable for use in developer compositions i.e. they must not affect the performance of, or cause precipitation of, the other components or be detrimental to the photographic material to be developed.
- the non-acidic organic component is selected from the group consisting of ethyl lactate and butyrolactone and the organic acid component is selected from the group consisting of formic acid and lactic acid.
- the photographic developer compositions of the present invention it is not necessary to dilute the developer concentrate obtained by mixing the two concentrates at the time the solutions are mixed. No finely divided solid 1-phenyl3-pyrazolidone is precipitated when the two concentrated solutions are mixed and the developer concentrate obtained by the use of the two solutions of the present invention is as stable as a corresponding l-phenyl-3- pyrazolidone-containing developer concentrate freshly prepared from its individual constituents. 'It is thus possible to mix the concentrates to give a standard developer concentrate which has satisfactory stability over the period of time normally required, i.e. up to two months at up to 30 C. temperatures, and which can be diluted in portions with Water to give working-strength developer solutions as required, thereby overcoming the difiiculties encountered with previously disclosed photographic developer compositions in the form of two solutions.
- a further advantage of the photographic developer compositions of the present invention is that the presence in the first, l-phenyl-3-pyraZolidone-containing, concentrate of an organic acid exerts a stabilising effect on the 1-phenyl-3-pyrazolidone in respect of hydrolysis due to the presence of water, thereby enabling the first solution to be other than completely non-aqueous and to contain up to w./v. of water without serious deterioration being encountered on storage for periods up to at least six months at 40 C. at temperatures ranging up to 50-55 C.
- solutions used in the present invention will, in general, be of as small a volume as is practicable having regard to the fact that the ingredients, particularly the lphenyl-3-pyrazolidone, should not crystallize out on prolonged standing at 0 C.
- a solution of 1-phenyl-3-pyrazolidone in a 2:1 v./v. mixture of butyrolactone and lactic acid containing g. of l-phenn yl-3-pyrazolidone per 100 ml. of solution is particularly suitable.
- the solution used in the second concentrate pack is, as already stated, a conventional l-phenyl-3-pyrazolidonecontaining developer from which the 1-phenyl-3-pyrazolidone has been omitted.
- developers ordinarily contain (besides l-phenyl-3-pyrazolidone) a polyhydric phenol as secondary developer, an alkali, an inorganic sulphite, an antifoggant, and, optionally a sequestering agent to prevent precipitation of metal ions in the working solutions and a buffering agent.
- the polyhydric phenol is generally hydroquinone, the alkali an alkali metal, for example sodium or potassium, hydroxide or carbonate, the inorganic sulphite an alkali metal, for example sodium or potassium, sulphite or metabisulphite, and the antifoggant an organic antifoggant, for example benzotriazole, or a source of bromide ions, for example an alkali metal, e.g. sodium or potassium, bromide.
- the sequestering agent which may be present is a sequestering agent for alkaline earth, particularly calcium, ions, for example N-hydroxyl ethyl-ethylenediamine N,N,N' triacetic acid trisodium salt or ethylenediaminetetraacetic acid tetrasodium salt.
- the buffering agent which may be present is usually a source of carbonate ions, for example an alkali metal, e.g. sodium or potassium, carbonate or bicarbonate, a source of borate ions, for example borax, an alkali metal, e.g. sodium or potassium, metaborate or boric acid, or a source of phosphate ions, for example an alkali metal, e.g.
- the second concentrate should contain enough alkali to ensure that the pH of the mixture of the two concentrates, after dilution to working-strength with further quantities of water, is 9.5 or above. This is important as the activity of the developer is unsatisfactory below this.
- a two solution pack developer composition in accordance with the present invention is prepared as follows:
- Second solution pack A solution is prepared from: G. Sodium metabisulphite 680 Potassium hydroxide 553 Benzotriazole 5.5 N-Hydroxyethyl-ethylenediamine-N,N',N-triacetic acid trisodium salt 15.0
- the two solutions may be mixed together to give a photographic developer concentrate, portions, or the whole, of which may be diluted with water in the ratio of 1 part by volume of concentrate to 4 parts by volume of water to give a working-strength developer solution having a pH value of 10.6.
- Process for the production of a photographic developer which comprises the steps of (1) providing a first concentrate in the form of a solution of 1-phenyl-3-pyrazolidone in a mixture of (a) butyrolacetone or ethyl lactate with (b) formic acid or lactic acid and a second concentrate in the form of a solution of a polyhydric phenol as secondary developer, an alkali, an inorganic sulphite, and an antifoggant, (2) mixing the said concentrates, and (3) diluting the mixture with water to produce a solution having a pH of at least 9.5.
- the first concentrate is a solution of l-phenyl-3-pyrazolidone in a 2:1 v./v. mixture of butyrolactone and lactic acid containing 10 g. of 1-phenyl-3-pyrazolidone per ml. of solution.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB42653/65A GB1154365A (en) | 1965-10-07 | 1965-10-07 | Photographic Silver Halide Developer Packs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3532498A true US3532498A (en) | 1970-10-06 |
Family
ID=10425380
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US583099A Expired - Lifetime US3532498A (en) | 1965-10-07 | 1966-09-29 | Photographic developer compositions |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3532498A (cs) |
| CH (1) | CH471408A (cs) |
| DK (1) | DK118751B (cs) |
| FR (1) | FR1495910A (cs) |
| GB (1) | GB1154365A (cs) |
| NL (1) | NL6614069A (cs) |
| NO (1) | NO123967B (cs) |
| SE (1) | SE333867B (cs) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0391154B1 (en) * | 1989-04-03 | 1997-11-12 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
| US6020113A (en) * | 1997-03-31 | 2000-02-01 | Fuji Photo Film Co., Ltd. | Process for producing photographic suspended processing agent composition |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3038801A (en) * | 1960-02-18 | 1962-06-12 | Philip A Hunt Company | Photographic pyrazolidone developers in non-aqueous organic solvents |
| US3178284A (en) * | 1960-04-14 | 1965-04-13 | May & Baker Ltd | Photographic developer compositions |
| US3369898A (en) * | 1963-09-05 | 1968-02-20 | Morton Int Inc | Stabilized 1-phenyl-3-pyrazolidone photographic developer system |
-
1965
- 1965-10-07 GB GB42653/65A patent/GB1154365A/en not_active Expired
-
1966
- 1966-09-29 US US583099A patent/US3532498A/en not_active Expired - Lifetime
- 1966-09-30 SE SE13183/66A patent/SE333867B/xx unknown
- 1966-10-05 FR FR78885A patent/FR1495910A/fr not_active Expired
- 1966-10-06 NO NO165035A patent/NO123967B/no unknown
- 1966-10-06 NL NL6614069A patent/NL6614069A/xx unknown
- 1966-10-06 CH CH1445666A patent/CH471408A/de not_active IP Right Cessation
- 1966-10-06 DK DK519666AA patent/DK118751B/da unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3038801A (en) * | 1960-02-18 | 1962-06-12 | Philip A Hunt Company | Photographic pyrazolidone developers in non-aqueous organic solvents |
| US3178284A (en) * | 1960-04-14 | 1965-04-13 | May & Baker Ltd | Photographic developer compositions |
| US3369898A (en) * | 1963-09-05 | 1968-02-20 | Morton Int Inc | Stabilized 1-phenyl-3-pyrazolidone photographic developer system |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0391154B1 (en) * | 1989-04-03 | 1997-11-12 | Minnesota Mining And Manufacturing Company | Concentrated photographic developer composition and method of making it |
| US6020113A (en) * | 1997-03-31 | 2000-02-01 | Fuji Photo Film Co., Ltd. | Process for producing photographic suspended processing agent composition |
Also Published As
| Publication number | Publication date |
|---|---|
| SE333867B (cs) | 1971-03-29 |
| NL6614069A (cs) | 1967-04-10 |
| NO123967B (cs) | 1972-02-07 |
| DK118751B (da) | 1970-09-28 |
| GB1154365A (en) | 1969-06-04 |
| FR1495910A (fr) | 1967-09-22 |
| CH471408A (de) | 1969-04-15 |
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