US2489728A - Monobasic salts of phosphate acids as stabilizers for diazotype prints - Google Patents
Monobasic salts of phosphate acids as stabilizers for diazotype prints Download PDFInfo
- Publication number
- US2489728A US2489728A US774438A US77443847A US2489728A US 2489728 A US2489728 A US 2489728A US 774438 A US774438 A US 774438A US 77443847 A US77443847 A US 77443847A US 2489728 A US2489728 A US 2489728A
- Authority
- US
- United States
- Prior art keywords
- prints
- diazotype
- stabilizers
- discoloration
- 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
- 150000003839 salts Chemical class 0.000 title description 3
- 239000003381 stabilizer Substances 0.000 title description 3
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 title 1
- 230000008878 coupling Effects 0.000 description 12
- 238000010168 coupling process Methods 0.000 description 12
- 238000005859 coupling reaction Methods 0.000 description 12
- 150000008049 diazo compounds Chemical class 0.000 description 12
- 238000002845 discoloration Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 238000005406 washing Methods 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 230000018109 developmental process Effects 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- 238000000354 decomposition reaction Methods 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 150000001340 alkali metals Chemical class 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 4
- 235000019799 monosodium phosphate Nutrition 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 4
- 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 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229960004838 phosphoric acid Drugs 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- LAXPFHMCFLHGKK-UHFFFAOYSA-N 4-diazo-n,n-dimethylcyclohexa-1,5-dien-1-amine Chemical compound CN(C)C1=CCC(=[N+]=[N-])C=C1 LAXPFHMCFLHGKK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000448280 Elates Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- YWBHIZNYYSZBFN-UHFFFAOYSA-M potassium;ethyl hydrogen phosphate Chemical compound [K+].CCOP(O)([O-])=O YWBHIZNYYSZBFN-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Images
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
- G03C5/18—Diazo-type processes, e.g. thermal development, or agents therefor
Definitions
- a carrier surface or base'lSe'aring a light-sensitive diazo compound rsexposeu to light of locally varied intensity (e. g. under a photographic transparency or an opaque design or line drawing on a transparent sheet) so as to destroy the diazo compound partly or completely in the illuminated ar'eas.
- the residual diazo'compound corre's'ponding tot image to be reproduced ' is coupled with arr" a'zo" coupling component, which may be originallyin: corporated with the dime compound on the car rier, or subsequentlyapplied theretoiria d'eveloper composition.
- Example 2 A series of prints prepared and developed in the same manner as in Example 1 and having strongly-contrasting image and background discoloration of a diazotype print, bearing residual unreacted coupling component and diazo compound decomposition products on the background areas thereof, which comprises the step of washing said print after its development with an aqueous solution of a compound having the general formula:
- R1 and R2 are selected from the group wherein R1 and R2 are selected from the group consisting of hydrogen and alkyl groups of 1 to 3 carbon atoms, and M is selected from the group areas, were washed with an aqueous solution,
- Example 3 A third set of prints prepared and developed as in Example 1 were washed with a 5% aqueous solution of sodium or potassium monoethyl hydro j gen phosphate, and thereupon dried. The copies thus obtained likewise possessed excellent stability to discoloration as was the case with the prints of the preceding examples.
- the corresponding ammonium salts can be used.
- other mono-alkali metal salts of lower alkyl (i. e. methyl, ethyl, propyl or isopropyl) monoor di-esters of phosphoric acid can be used instead of the sodium or potassium ethyl hydrogenphosphate in Example 3.
- the pH of the washing solution in-each of the foregoing examples is between 5 and 7.
- small amounts of buffers, acids or alkalies can be added to adjust the pH of the solution to the aforesaid range.
- small amounts of acid may be advantageously used in connection with mono alkali metal dialkyl phosphates.
- the washing treatment of my invention can be applied with a similarly advantageous effect to diazotype prints having other kinds of bases or carriers (e. g. ordinary paper, cellulosic films or the like).
- Iclaim 1. The process for, improving the stability to consisting of hydrogen and alkyl groups of 1 to 3 carbon atoms, and M is selected from the group consisting of alkali metals and the ammonium radical, said solution having a pH of at least '5 and less than 7.
- R1 and R2 are selected from the group consisting of hydrogen and alkyl groups of l to 3 carbon atoms, and M is selected from the group consisting of alkali metals and the ammonium radical, said solution having a pH of at least 5 and less than 7.
- R, o 1 o wherein R1 and R2 are selected from the group consisting of hydrogen and alkyl groups of 1 to 3 carbon atoms, and M is selected from the group consisting of alkali metals and the ammonium radical, said solution having a pH of at least 5 and less than 7.
- the process for improving the stability to discoloration of a' diazotype print, bearing reside ual unreacted coupling component and diazo compound decomposition products on the background areas thereof, which comprises the step of washing said print after its development with an aqueous solution of sodium dihydrogen phosphate.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
Patented Nov. 29, 1949 UNITED STATES-- 2,489,728 M 'NQB .S L D iiQSIHKTE 1 1 .38" AS STABILIZERS'IFOR DIAZOTYPE PRINTS sum 0. Slifki n; BifigTiamton Nl Y.',- assignof to I General Anilir'ie"& Film Corporation; New York; N. Y., a eorpora-t'iomof Delaware No Drawing; Application September 1 6 1 9 47 Serial No. 774',4 38- This inventionr'elates to an'improvem fitinthe production of photographic prints 'b'ytli' diaz'o typeproee'ss. I
In the preparation of diazotyp' prints asordi narilycarriedout, a carrier surface or base'lSe'aring a light-sensitive diazo compound rsexposeu to light of locally varied intensity (e. g. under a photographic transparency or an opaque design or line drawing on a transparent sheet) so as to destroy the diazo compound partly or completely in the illuminated ar'eas. Indeveloping the print; the residual diazo'compound corre's'ponding tot image to be reproduced 'is coupled with arr" a'zo" coupling component, which may be originallyin: corporated with the dime compound on the car rier, or subsequentlyapplied theretoiria d'eveloper composition. When the azo couplingfcomponent is originally present together" with the light-sensitive diazo compound" on the" photoprinting material; development cambe'advant geou's'ly efiected by the dry process '(i'i'e. bye posure' to an alkaline vapor such: asammonia). Such prints can also" be developed by a semi wet process wherein the exposed print'ifi'moistene'tf with small amounts of a solution adapted to effeet coupling (e. g. a solution of alkaline reacting substance), such solution being allowed to dry on the resulting print. When no coupling component' is included'in the photopifinting' material; it may be-applied together withthe alkaline reagent" which promotes coupling in the solution "em-"'- ployed in the semi-wet developing p'rocessr I In the aforesaid dry and semi-wet developing processes, the excess coupling component-and also" decomposition products of the light sensitive' diazo compound, remain on the surface; of'the finished print, particularly in the background areas. These materials causeseriousdiscoloraf tion' of the background on exposure of the print to light and/or air, whereby the appearance and '4 clarity of the copy is seriously impaired. Numei ous attempts have been made to" improve the aging qualities of such prints, for example by incorporating stabilizers in the sensitizing or developing composition, but such proposals are generally only partly efiective.
It has also been proposed to remove-the injurious byproducts and excess couplingcomponenpm by" washing the developed print with water; Considerable improvement is effected thereby insofar as-the stability ofthe background to discol-' oration is concerned, but such treatment often 1 causes undesirable color changes in-thedeveloped image. For example,- black dyed prints Whenwashed with water have a marked tendency to b wherein arange of 'shadows of varying' depth butr 2- of the-samecolor (particul'arly blaclr) is to be pro-" du'cedr I- have diseovered-'-thatdiaZotype prints:proidu'ced -by the dr'y-or semi-'wet development prod-'- esses andtherefore: carrying substantial amounts of coupler and diazo compound decompositionw products on the surface oi the print, can be effectively stabilized against 'disiicilr'ifation on exposure to light and/or air without causing undesirable thangesin the 061"" of theimage} by washing the pri'fi'ts 'withan aqueous solution of a water-$5111 bl iiiorio b'asic aw of a" phosphate acid, particularly' a mono-alkali metal or ammonium salt" of rrosphtricaeid-or of lower alkyl mono: or" diesters of phosphoric-acid the; solution having 5 PH of at least'5 andless than 7.
Phosphoric acids employed at. cordanee'withmy inven on may be represented by"thefollowin'g"general formula"? corisi'sting' of (i.e-alkyl= g-rou-p is se'le'cite'dno" the? group consis metals and the ammonium" The aforesaid-seem; fpr'e'srited by thephov' formula; are advantageously: employedinf an aqueous sohil'liori 'in ga coheentraubnor atlea 1% 'an'd preferably 6F'about--5%c Wherrthe col compound-of the ima e is relatively soluble in w te1-,'-'a-r1y tendency of e color to run during th washing treatment-can overcome by including a neutral salt (629. NtiCBGr Na'zSOr) ifr-the wa sh ing s'olution for exampl in a concentration o'f about"5% .3
'thewashingr treatment is coirip1ete; -the print-1s allowed to d rs i The resmtihg:co ies'are sub'sta'n'tially =imrtiu-rle to discoloration upon e posur'e' to light: aridlo air;-andthe* co1oi ofthe print as originallydeveloped is preserved witho' change, even when the seiis'iti'z'ed' base materialis adayer'of gelatin" Y H Myiinventiomis illustratedby 'the following ex amplesw ting or 'allalr- Example 1 tized in the usual manner by impregnation with sensitizing compositions containing the following combinations of diazo compound and coupler:
A. 2-diazo-l-naphtholl-sulfonic acid and phloroglucinol B. p-Diazo-diphenylamine sulfate and 2-naphthol-3,6-disodium sulfonate C. Zinc chloride double salt of p-diazo dimethylaniline and 2,3-dihydroxynaphthalene The developed prints were washed in accordance with my invention with'a 5% aqueous solution of sodium dihydrogen phosphate and thereupon dried. The resulting washed copies showed no yellowing or discoloration'on exposure to light and air for prolonged periods, and the'color of the print as originally developed remained unchanged.
Example 2 A series of prints prepared and developed in the same manner as in Example 1 and having strongly-contrasting image and background discoloration of a diazotype print, bearing residual unreacted coupling component and diazo compound decomposition products on the background areas thereof, which comprises the step of washing said print after its development with an aqueous solution of a compound having the general formula:
, wherein R1 and R2 are selected from the group wherein R1 and R2 are selected from the group consisting of hydrogen and alkyl groups of 1 to 3 carbon atoms, and M is selected from the group areas, were washed with an aqueous solution,
containing 5% sodium dihydrogen phosphate and 5% sodium chloride and thereupon dried. The. copies thus obtained possessed stability against.
discoloration similar to that obtained in the foregoing example, and the edges of the image portion were perfectly defined, showing no tendency of the color to run.
Example 3' A third set of prints prepared and developed as in Example 1 were washed with a 5% aqueous solution of sodium or potassium monoethyl hydro j gen phosphate, and thereupon dried. The copies thus obtained likewise possessed excellent stability to discoloration as was the case with the prints of the preceding examples.
Instead of the sodium or potassium salts employed in the foregoing examples, the corresponding ammonium salts can be used. Similarly, other mono-alkali metal salts of lower alkyl (i. e. methyl, ethyl, propyl or isopropyl) monoor di-esters of phosphoric acid can be used instead of the sodium or potassium ethyl hydrogenphosphate in Example 3. The pH of the washing solution in-each of the foregoing examples is between 5 and 7. If necessary, small amounts of buffers, acids or alkalies can be added to adjust the pH of the solution to the aforesaid range. For example, small amounts of acid may be advantageously used in connection with mono alkali metal dialkyl phosphates. The washing treatment of my invention can be applied with a similarly advantageous effect to diazotype prints having other kinds of bases or carriers (e. g. ordinary paper, cellulosic films or the like). I
Iclaim: 1. The process for, improving the stability to consisting of hydrogen and alkyl groups of 1 to 3 carbon atoms, and M is selected from the group consisting of alkali metals and the ammonium radical, said solution having a pH of at least '5 and less than 7.
2. The process for improving the stability to discoloration of a diazotype print, bearing residual unreacted coupling component and diazo compound decomposition products on the back-. ground areas thereof, which comprises the step of washing said print after its development with an aqueous solution of a neutral water-soluble inorganic salt and a compound having the gen-. "eral formula:
consisting of alkali metals and the ammonium radical, said solution having a pH of at least 5 and less than 7.
3. The process for improving the stability to discoloration of a diazotype print, bearing residual unreacted coupling component and diazo compound decomposition products on the back ground areas thereof, which comprises the step'. of washing said print after its development with.
an aqueous solution containing at least 1% of a compound having the general formula:
wherein R1 and R2 are selected from the group consisting of hydrogen and alkyl groups of l to 3 carbon atoms, and M is selected from the group consisting of alkali metals and the ammonium radical, said solution having a pH of at least 5 and less than 7.
4, The process for improving the stability to discoloration of a diazotype print, bearing resid---- ual unreacted coupling component and diazocompound decomposition products on the back-,
ground areas thereof, which comprises the step of washing said print after its development with an aqueous solution containing 5% by weight of;
a compound having the general formula:
Rz-O
R, o 1 =o wherein R1 and R2 are selected from the group consisting of hydrogen and alkyl groups of 1 to 3 carbon atoms, and M is selected from the group consisting of alkali metals and the ammonium radical, said solution having a pH of at least 5 and less than 7.
5. The process for improving the stability to discoloration of a' diazotype print, bearing reside ual unreacted coupling component and diazo compound decomposition products on the background areas thereof, which comprises the step of washing said print after its development with an aqueous solution of sodium dihydrogen phosphate.
6. The process for improving the stability to discoloration of a diazotype print, bearing residual unreacted coupling component and diazo compound decomposition products on the background areas thereof, which comprises the step of washing said print after its development with an aqueous solution containing sodium dihydrogen phosphate and sodium chloride.
7. The process for improving the stability to discoloration of a diazotype print, bearing residual unreacted coupling component and diazo REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,967,371 Schmidt et a1 July 24, 1934 15 2,113,944 Leuch Apr. 12, 1938 2,442,061 Slifkin May 25, 1948
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US774438A US2489728A (en) | 1947-09-16 | 1947-09-16 | Monobasic salts of phosphate acids as stabilizers for diazotype prints |
| GB14138/48A GB641323A (en) | 1947-09-16 | 1948-05-25 | After-treatment for diazotype prints |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US774438A US2489728A (en) | 1947-09-16 | 1947-09-16 | Monobasic salts of phosphate acids as stabilizers for diazotype prints |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2489728A true US2489728A (en) | 1949-11-29 |
Family
ID=25101227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US774438A Expired - Lifetime US2489728A (en) | 1947-09-16 | 1947-09-16 | Monobasic salts of phosphate acids as stabilizers for diazotype prints |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2489728A (en) |
| GB (1) | GB641323A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2776888A (en) * | 1954-07-15 | 1957-01-08 | Pop Gregorio | Photographic sensitizer and developer |
| US3110596A (en) * | 1958-08-08 | 1963-11-12 | Azoplate Corp | Process for simultaneously developing and fixing printing plates |
| US3173788A (en) * | 1960-02-10 | 1965-03-16 | Gen Aniline & Film Corp | Developing positive working photolitho-graphic printing plates containing diazo oxides |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1967371A (en) * | 1931-03-28 | 1934-07-24 | Kalle & Co Ag | Process of preparing copies |
| US2113944A (en) * | 1933-09-11 | 1938-04-12 | Dietzgen Eugene Co | Production of photographic diazotype prints |
| US2442061A (en) * | 1944-09-26 | 1948-05-25 | Gen Aniline & Film Corp | Acid stabilized light-sensitive diazotype coating |
-
1947
- 1947-09-16 US US774438A patent/US2489728A/en not_active Expired - Lifetime
-
1948
- 1948-05-25 GB GB14138/48A patent/GB641323A/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1967371A (en) * | 1931-03-28 | 1934-07-24 | Kalle & Co Ag | Process of preparing copies |
| US2113944A (en) * | 1933-09-11 | 1938-04-12 | Dietzgen Eugene Co | Production of photographic diazotype prints |
| US2442061A (en) * | 1944-09-26 | 1948-05-25 | Gen Aniline & Film Corp | Acid stabilized light-sensitive diazotype coating |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2776888A (en) * | 1954-07-15 | 1957-01-08 | Pop Gregorio | Photographic sensitizer and developer |
| US3110596A (en) * | 1958-08-08 | 1963-11-12 | Azoplate Corp | Process for simultaneously developing and fixing printing plates |
| US3173788A (en) * | 1960-02-10 | 1965-03-16 | Gen Aniline & Film Corp | Developing positive working photolitho-graphic printing plates containing diazo oxides |
Also Published As
| Publication number | Publication date |
|---|---|
| GB641323A (en) | 1950-08-09 |
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