US2501874A - Photographic diazo-sensitized glassine paper - Google Patents
Photographic diazo-sensitized glassine paper Download PDFInfo
- Publication number
- US2501874A US2501874A US676224A US67622446A US2501874A US 2501874 A US2501874 A US 2501874A US 676224 A US676224 A US 676224A US 67622446 A US67622446 A US 67622446A US 2501874 A US2501874 A US 2501874A
- Authority
- US
- United States
- Prior art keywords
- glassine paper
- prints
- base
- acid
- photographic
- 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
- 239000011086 glassine Substances 0.000 title claims description 23
- 239000000463 material Substances 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 25
- 230000001235 sensitizing effect Effects 0.000 claims description 18
- 230000007704 transition Effects 0.000 claims description 11
- 230000008878 coupling Effects 0.000 claims description 9
- 238000010168 coupling process Methods 0.000 claims description 9
- 238000005859 coupling reaction Methods 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- 241000238370 Sepia Species 0.000 claims description 5
- 150000008049 diazo compounds Chemical class 0.000 claims description 5
- 229920002678 cellulose Polymers 0.000 claims description 4
- 231100000202 sensitizing Toxicity 0.000 description 17
- 239000000543 intermediate Substances 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 239000000123 paper Substances 0.000 description 7
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 229920002301 cellulose acetate Polymers 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 4
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000001989 diazonium salts Chemical class 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000000987 azo dye Substances 0.000 description 2
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229960003742 phenol Drugs 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
- AHCDXLAGLYNTIA-UHFFFAOYSA-N 1-n-ethyl-2-methylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(N)C=C1C AHCDXLAGLYNTIA-UHFFFAOYSA-N 0.000 description 1
- GJMFIOIYHBJNOY-UHFFFAOYSA-N 2-(4-amino-n-methylanilino)ethanol Chemical compound OCCN(C)C1=CC=C(N)C=C1 GJMFIOIYHBJNOY-UHFFFAOYSA-N 0.000 description 1
- YCIYKQSGEUKDSZ-UHFFFAOYSA-N 2-(4-methylphenyl)-1h-pyrazol-5-one Chemical compound C1=CC(C)=CC=C1N1N=C(O)C=C1 YCIYKQSGEUKDSZ-UHFFFAOYSA-N 0.000 description 1
- ZILVNHNSYBNLSZ-UHFFFAOYSA-N 2-(diaminomethylideneamino)guanidine Chemical compound NC(N)=NNC(N)=N ZILVNHNSYBNLSZ-UHFFFAOYSA-N 0.000 description 1
- UYEMGAFJOZZIFP-UHFFFAOYSA-N 3,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC(O)=C1 UYEMGAFJOZZIFP-UHFFFAOYSA-N 0.000 description 1
- RGCITEKHKXPDDH-UHFFFAOYSA-N 4-(diethylamino)benzenediazonium Chemical compound CCN(CC)C1=CC=C([N+]#N)C=C1 RGCITEKHKXPDDH-UHFFFAOYSA-N 0.000 description 1
- YFCXTPKUVYRXFI-UHFFFAOYSA-M 4-(diethylamino)benzenediazonium;chloride Chemical compound [Cl-].CCN(CC)C1=CC=C([N+]#N)C=C1 YFCXTPKUVYRXFI-UHFFFAOYSA-M 0.000 description 1
- QNGVNLMMEQUVQK-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C=C1 QNGVNLMMEQUVQK-UHFFFAOYSA-N 0.000 description 1
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- CLMIXJSUEGDXTI-UHFFFAOYSA-N B(F)(F)F.C(C)N(C1=CC=C(C=C1)[N+]#N)CC Chemical compound B(F)(F)F.C(C)N(C1=CC=C(C=C1)[N+]#N)CC CLMIXJSUEGDXTI-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- XMCGFZFVFXXELK-UHFFFAOYSA-N C1(=CC=C(C=C1)N)N.C(C)NC1=CC=C(N)C=C1 Chemical compound C1(=CC=C(C=C1)N)N.C(C)NC1=CC=C(N)C=C1 XMCGFZFVFXXELK-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 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
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- HTKFORQRBXIQHD-UHFFFAOYSA-N allylthiourea Chemical compound NC(=S)NCC=C HTKFORQRBXIQHD-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- OXAUNDBQHKIUSD-UHFFFAOYSA-N azanium;titanium;fluoride Chemical compound [NH4+].[F-].[Ti] OXAUNDBQHKIUSD-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process 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
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HKQOBOMRSSHSTC-UHFFFAOYSA-N cellulose acetate Chemical compound OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(O)C(O)C1O.CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(COC(C)=O)O1.CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 HKQOBOMRSSHSTC-UHFFFAOYSA-N 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003230 hygroscopic agent Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- MGJXBDMLVWIYOQ-UHFFFAOYSA-N methylazanide Chemical compound [NH-]C MGJXBDMLVWIYOQ-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- CNXZLZNEIYFZGU-UHFFFAOYSA-N n-(4-amino-2,5-diethoxyphenyl)benzamide Chemical compound C1=C(N)C(OCC)=CC(NC(=O)C=2C=CC=CC=2)=C1OCC CNXZLZNEIYFZGU-UHFFFAOYSA-N 0.000 description 1
- GPUMPJNVOBTUFM-UHFFFAOYSA-N naphthalene-1,2,3-trisulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC2=C1 GPUMPJNVOBTUFM-UHFFFAOYSA-N 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-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
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000010491 poppyseed oil Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- QPILZZVXGUNELN-UHFFFAOYSA-M sodium;4-amino-5-hydroxynaphthalene-2,7-disulfonate;hydron Chemical compound [Na+].OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S([O-])(=O)=O)=CC2=C1 QPILZZVXGUNELN-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C1/00—Pressure vessels, e.g. gas cylinder, gas tank, replaceable cartridge
- F17C1/02—Pressure vessels, e.g. gas cylinder, gas tank, replaceable cartridge involving reinforcing arrangements
- F17C1/04—Protecting sheathings
- F17C1/06—Protecting sheathings built-up from wound-on bands or filamentary material, e.g. wires
-
- 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
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
Definitions
- the present invention relates to the manufacture of photographic diazotype materials having particular utility in the preparation of intermediate or transition prints and more particularly to the base of such diazotype materials to which the sensitizing composition is applied.
- the diazotype process which is of rather general application in the formation of prints from original patterns, has become increasingly more importantin the preparation of transition prints or intermediate prints on a transparent base stock for the purpose of reproducing drawings, or ginals of old manuscripts and the like.
- the efiiciency of these prints depends upon a number of factors, to wit, the opacity of the azo dye image formed to ultraviolet light, the transparency of the background, the speed at which the intermediate print may be reproduced, and the like.
- diazotype materials which yield valuable transition or intermediate prints.
- These diazotype materials are prepared with a transparent support such as transparentized paper, i. e., rag paper, cellulose esters such as cellulose acetate, and the like.
- transparentized paper i. e., rag paper
- cellulose esters such as cellulose acetate, and the like.
- diazotype materials do not represent the ultimate from a practical standpoint, particularly as regards contrast, line density, speed of duplication and the like.
- a further object of the present invention is to produce photographic diazotype materials having a glassine paper base, said materials having the ability to permit duplication at a much greater rate than any materials of a like nature presently known.
- the glassine paper which is to serve as the base is commercially available and may be prepared according to, for example, U. S. P. 1,914,798 and 1,914,799. While different weights of paper may be used for the preparation of the lightsensitivematerials, I have discovered that best results are obtained when utilizing a 25-pound weight paper (500 sheets, 24 by 36 inches).
- Glassine paper in and of itself is not particularly strong. It is therefore preferable to incorporate in the coating composition an organic film forming material to thereby increase the strength of the base.
- Any organic film forming material either water-insoluble or Water-soluble may be employed, so long as it is transparent in a thin layer such as a layer having a thickness of .01 inch or less. Film forming materials which meet this requirement are known and are available on the open market.
- suitable water-insolublefilm forming materials are: polystyrene, polyacrylic acid esters such as the methyl or ethyl ester, polymethacrylic acid ester such as the methyl or ethyl ester, the copolymers of vinyl chloride and a vinyl ester such as vinyl acetate, copolymers of maleic anhydride and styrene, copolymers of vinylidine chloride and vinyl acetate, alkyd resins such as those derived from phthalic acid and glycerol, phthalic acid and sorbitol, phthalic acid, glycerol and a drying oil, such as poppyseed oil, cellulose esters such as cellulose acetate, cellulose acetate-butyrate, cellulose propionate, cellulose acetate-propionate, linear superpolymers such as linear superpolyamides, linear superpolyurethanes, linear superpolyureas and the like.
- organic film forming materials such as organic
- the sensitizing composition containing'such material is applied from a solution of the ingredients in an organic solvent.
- resin solvents such as acetone, butyl acetate, benzyl alcohol, butyl alcohol, mixtures of ethers and alcohols such as a mixture of ethanol and ethyl ether, chlorinated hydrocarbons such as chloroform, ethylene chloride, and mixtures of such chlorinated hydrocarbons with alcohols or ethers such as ethylene chloride and butyl chloride and diethyl ether and the like.
- the light-sensitive diazonium compounds employed in the sensitizing composition are those generally utilized in the manufacture of diazotype papers but are preferably of the class of the paraphenylene diamines.
- Such coupling components are the phenols, particularly the polyhydric phenols and their derivatives, such as resorcinol, resorcinol monoand disulfonic acids, phenol itself, 2- (omega-phenylamino) -methyl-l-hydroxybenzene, p (2 hydroxyphenyD-propionic acid, and similar compounds referred to in U. S. P. 2,245,628, 2.7-dihydroxynaphthalene (U. S. P. 1,758,676) phloroglucinol and the like.
- Such coupling components will hereinafter be referred to as phenolic coupling components capable of yielding with the usual diazos, azo dyestuff images having a yellow or sepia tone.
- the sensitizing compositions may contain the usual adjuncts such as metal salts, to intensify the dyestuif image, i. e., aluminum sulfate, titanium ammonium fluoride, nickel sulfate and the like, stabilizing agents such as thiourea, thiosinamine, naphthalene trisulfonic acid and the like, acids designed to retard precoupling such as citric acid, maleic acid, tartaric acid, boric acid and the like, hygroscopic agents such as glycol, glycerin, dextrin and the like.
- adjuncts such as metal salts, to intensify the dyestuif image, i. e., aluminum sulfate, titanium ammonium fluoride, nickel sulfate and the like
- stabilizing agents such as thiourea, thiosinamine, naphthalene trisulfonic acid and the like
- acids designed to retard precoupling such as citric acid, maleic
- the sensitizing compositions In making up the sensitizing compositions, one uses the amounts of diazo compound, coupling component and the other usual adjuncts customary in the art. If desired, however, one may also employ a slight excess of the diazo and coupling component although as ageneral rule this is unnecessary.
- the quantity of the resin which is to be employed will vary from about 5 to 20 per cent by weight of the composition and is preferably about 10 per cent.
- the quantity of the sensitizing composition which is applied to the base ranges from about 10 to 12 per cent by weight of the base.
- Example 1 25-pound glassine paper is coated in an apparatus of the type shown in the drawing on both faces with a sensitizing composition having the following ingredients:
- Example II Glassine paper prepared according to USP 1,914,798 or 1,914,799 is simultaneously coated on both faces with a composition prepared as follows:
- photographic diazotype glassine papers referred to hereinabove have been described as particularly suitable for the preparation of transition or intermediate prints. It is to be pointed out, however, that such photographic diazotype papers have many other applications such as, for example, overlays used for multicolored prints, especially semi-transparent Wrappers, lamp-shades and the like. When so utilized, it is unnecessary to select coupling components which yield yellow or sepia toned azo dyes inasmuch as the question of ultraviolet light opacity is not of particular moment in these applications.
- dihgdroxynaphthalene dihgdroxynaphthalene. It is therefore to be understood that the invention in its broadest aspects contemplates photographic diazotype materials in which a sensitizing composition comprising a diaio component and an azo dyecoupling component are applied to a glassine paper base.
- Transparent diazotype materials particular- 1y suitable for the preparation of intermediate or transition prints comprising a glassine paper base having applied to both faces thereof a sensitiz ing composition comprising a light-sensitive diazo compound, a small quantity of a resinous low viscosity cellulose ester film forming material and a phenolic coupling component capable of yielding with the diazo compound anazo dye having atone selected from the class consisting of yellojw and sepia tones.
- Transparent diazotype materials particularly suitable for the production of transition and intermediate prints comprising a glassine paper base having applied to both surfaces thereof a sensitizing composition comprising a low viscosity cellulose acetate, p-diethylaminobenzene diazonium borofluoride and resorcinol.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US676224A US2501874A (en) | 1946-06-12 | 1946-06-12 | Photographic diazo-sensitized glassine paper |
| GB10644/47A GB625999A (en) | 1946-06-12 | 1947-04-21 | Photographic diazotype materials particularly suitable for preparing intermediate prints |
| FR947487D FR947487A (fr) | 1946-06-12 | 1947-06-03 | Matériels photographiques diazotypes |
| CH267973D CH267973A (fr) | 1946-06-12 | 1947-06-11 | Matériel photosensible du type diazo. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US676224A US2501874A (en) | 1946-06-12 | 1946-06-12 | Photographic diazo-sensitized glassine paper |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2501874A true US2501874A (en) | 1950-03-28 |
Family
ID=24713681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US676224A Expired - Lifetime US2501874A (en) | 1946-06-12 | 1946-06-12 | Photographic diazo-sensitized glassine paper |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2501874A (fr) |
| CH (1) | CH267973A (fr) |
| FR (1) | FR947487A (fr) |
| GB (1) | GB625999A (fr) |
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2595916A (en) * | 1947-04-21 | 1952-05-06 | Grinten Chem L V D | Light sensitive positive printing diazotype paper having a calendered surface |
| US2774669A (en) * | 1953-04-13 | 1956-12-18 | Dick Co Ab | Diazotype reproduction process |
| DE1040371B (de) * | 1954-03-22 | 1958-10-02 | Renker Belipa G M B H | Verfahren zur Herstellung von mit lichtempfindlichen Diazo-verbindungen praeparierten Unterlagen |
| DE1045799B (de) * | 1955-02-09 | 1958-12-04 | Ozalid Co Ltd | Verfahren zur Herstellung von Diazotypiematerial |
| DE973598C (de) * | 1951-03-20 | 1960-04-07 | Grinten Chem L V D | Lichtempfindliches Diazotypiematerial |
| US3002851A (en) * | 1957-03-28 | 1961-10-03 | Horizons Inc | Photosensitized transparent element |
| US3032414A (en) * | 1956-11-19 | 1962-05-01 | Kalvar Corp | System of photographic reproduction |
| US3069268A (en) * | 1958-07-10 | 1962-12-18 | Gen Aniline & Film Corp | Method for improving the tonal gradation of diazotype materials using stratified sensitizing components and u. v. filters |
| US3153592A (en) * | 1962-05-15 | 1964-10-20 | Dietzgen Co Eugene | Complex salt diazotype photoprinting materials |
| US3161510A (en) * | 1961-10-26 | 1964-12-15 | Western Electric Co | Visual aid technique of presenting drawing changes |
| US3370949A (en) * | 1962-11-15 | 1968-02-27 | Lichtdrukpapierfabriek De Atla | Process of preparing transparentized double face photoprinting material for the so-called dry process |
| US3431109A (en) * | 1964-10-16 | 1969-03-04 | Addressograph Multigraph | Heat sensitive diazotype materials |
| US3466172A (en) * | 1967-01-13 | 1969-09-09 | Ibm | Method of using photographic vesicular and diazo films having diazo antihalation layers |
| US3484241A (en) * | 1967-01-16 | 1969-12-16 | Ibm | Diazo type films with extended linear latitude |
| DE1572088A1 (de) * | 1966-10-18 | 1970-02-19 | Kalle Ag | Zweikomponenten-Diazotypiematerial fuer die Herstellung von Zwischenoriginalen |
| US3620740A (en) * | 1968-01-09 | 1971-11-16 | Agfa Gevaert Nv | Thermodiazo-type copying |
| US3773511A (en) * | 1969-10-14 | 1973-11-20 | Microseal Corp | Film record card system |
| US3779758A (en) * | 1969-03-25 | 1973-12-18 | Photocircuits Corp | Photosensitive process for producing printed circuits employing electroless deposition |
| US3915709A (en) * | 1973-04-13 | 1975-10-28 | Gaf Corp | Backwetting coating for diazo microfilm |
| US3923518A (en) * | 1973-04-10 | 1975-12-02 | Andrews Paper & Chem Co Inc | Erasable diazotype material with vinyl chloride and methyl acrylate copolymer interlayer |
| US4508808A (en) * | 1982-11-12 | 1985-04-02 | Xidex Corporation | Method of using diazotype photographic materials with preexposure treatment to form uniform sites of refractive index change |
Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US328431A (en) * | 1885-10-13 | Thomas c | ||
| US656751A (en) * | 1899-08-09 | 1900-08-28 | Arthur Schwarz | Sensitized photographic paper. |
| US1756400A (en) * | 1926-02-22 | 1930-04-29 | Kalle & Co Ag | Light-sensitive materials and process of making them |
| GB409134A (en) * | 1932-04-18 | 1934-04-26 | Jaroslav Karafiat | Process for preparing light sensitive layers on foils of regenerated cellulose |
| US1964358A (en) * | 1931-10-19 | 1934-06-26 | Kalle & Co Ag | Light-sensitive layers containing a titanium salt of an organic hydroxy acid and process of preparing them |
| GB443955A (en) * | 1934-08-10 | 1936-03-10 | Halden & Co Ltd J | Improvements in and relating to diazo-type printing processes |
| GB450817A (en) * | 1935-05-02 | 1936-07-24 | Halden & Co Ltd J | Improvements in and relating to diazo type printing processes |
| US2239704A (en) * | 1938-02-10 | 1941-04-29 | Hartford Nat Bank & Trust Co | Light-sensitive layer and method of making the same |
| GB536714A (en) * | 1940-04-15 | 1941-05-23 | Le Film Ozaphane Sa | Improvements in or relating to light-sensitive photographic films |
| US2245628A (en) * | 1937-04-05 | 1941-06-17 | Helge Svenson | Reflex copying process |
| US2246425A (en) * | 1938-06-18 | 1941-06-17 | Kalle & Co Ag | Production of diazotype reflex copies |
| US2378583A (en) * | 1939-12-27 | 1945-06-19 | Schmidt Maximilian Paul | Photographic printing material |
| US2405523A (en) * | 1944-08-09 | 1946-08-06 | Du Pont | Light-sensitive photographic compositions and elements |
-
1946
- 1946-06-12 US US676224A patent/US2501874A/en not_active Expired - Lifetime
-
1947
- 1947-04-21 GB GB10644/47A patent/GB625999A/en not_active Expired
- 1947-06-03 FR FR947487D patent/FR947487A/fr not_active Expired
- 1947-06-11 CH CH267973D patent/CH267973A/fr unknown
Patent Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US328431A (en) * | 1885-10-13 | Thomas c | ||
| US656751A (en) * | 1899-08-09 | 1900-08-28 | Arthur Schwarz | Sensitized photographic paper. |
| US1756400A (en) * | 1926-02-22 | 1930-04-29 | Kalle & Co Ag | Light-sensitive materials and process of making them |
| US1964358A (en) * | 1931-10-19 | 1934-06-26 | Kalle & Co Ag | Light-sensitive layers containing a titanium salt of an organic hydroxy acid and process of preparing them |
| GB409134A (en) * | 1932-04-18 | 1934-04-26 | Jaroslav Karafiat | Process for preparing light sensitive layers on foils of regenerated cellulose |
| GB443955A (en) * | 1934-08-10 | 1936-03-10 | Halden & Co Ltd J | Improvements in and relating to diazo-type printing processes |
| GB450817A (en) * | 1935-05-02 | 1936-07-24 | Halden & Co Ltd J | Improvements in and relating to diazo type printing processes |
| US2245628A (en) * | 1937-04-05 | 1941-06-17 | Helge Svenson | Reflex copying process |
| US2239704A (en) * | 1938-02-10 | 1941-04-29 | Hartford Nat Bank & Trust Co | Light-sensitive layer and method of making the same |
| US2246425A (en) * | 1938-06-18 | 1941-06-17 | Kalle & Co Ag | Production of diazotype reflex copies |
| US2378583A (en) * | 1939-12-27 | 1945-06-19 | Schmidt Maximilian Paul | Photographic printing material |
| GB536714A (en) * | 1940-04-15 | 1941-05-23 | Le Film Ozaphane Sa | Improvements in or relating to light-sensitive photographic films |
| US2405523A (en) * | 1944-08-09 | 1946-08-06 | Du Pont | Light-sensitive photographic compositions and elements |
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2595916A (en) * | 1947-04-21 | 1952-05-06 | Grinten Chem L V D | Light sensitive positive printing diazotype paper having a calendered surface |
| DE973598C (de) * | 1951-03-20 | 1960-04-07 | Grinten Chem L V D | Lichtempfindliches Diazotypiematerial |
| US2774669A (en) * | 1953-04-13 | 1956-12-18 | Dick Co Ab | Diazotype reproduction process |
| DE1040371B (de) * | 1954-03-22 | 1958-10-02 | Renker Belipa G M B H | Verfahren zur Herstellung von mit lichtempfindlichen Diazo-verbindungen praeparierten Unterlagen |
| DE1045799B (de) * | 1955-02-09 | 1958-12-04 | Ozalid Co Ltd | Verfahren zur Herstellung von Diazotypiematerial |
| US3032414A (en) * | 1956-11-19 | 1962-05-01 | Kalvar Corp | System of photographic reproduction |
| US3002851A (en) * | 1957-03-28 | 1961-10-03 | Horizons Inc | Photosensitized transparent element |
| US3069268A (en) * | 1958-07-10 | 1962-12-18 | Gen Aniline & Film Corp | Method for improving the tonal gradation of diazotype materials using stratified sensitizing components and u. v. filters |
| US3161510A (en) * | 1961-10-26 | 1964-12-15 | Western Electric Co | Visual aid technique of presenting drawing changes |
| US3153592A (en) * | 1962-05-15 | 1964-10-20 | Dietzgen Co Eugene | Complex salt diazotype photoprinting materials |
| US3370949A (en) * | 1962-11-15 | 1968-02-27 | Lichtdrukpapierfabriek De Atla | Process of preparing transparentized double face photoprinting material for the so-called dry process |
| US3431109A (en) * | 1964-10-16 | 1969-03-04 | Addressograph Multigraph | Heat sensitive diazotype materials |
| DE1572088A1 (de) * | 1966-10-18 | 1970-02-19 | Kalle Ag | Zweikomponenten-Diazotypiematerial fuer die Herstellung von Zwischenoriginalen |
| US3466172A (en) * | 1967-01-13 | 1969-09-09 | Ibm | Method of using photographic vesicular and diazo films having diazo antihalation layers |
| US3484241A (en) * | 1967-01-16 | 1969-12-16 | Ibm | Diazo type films with extended linear latitude |
| US3620740A (en) * | 1968-01-09 | 1971-11-16 | Agfa Gevaert Nv | Thermodiazo-type copying |
| US3779758A (en) * | 1969-03-25 | 1973-12-18 | Photocircuits Corp | Photosensitive process for producing printed circuits employing electroless deposition |
| US3773511A (en) * | 1969-10-14 | 1973-11-20 | Microseal Corp | Film record card system |
| US3923518A (en) * | 1973-04-10 | 1975-12-02 | Andrews Paper & Chem Co Inc | Erasable diazotype material with vinyl chloride and methyl acrylate copolymer interlayer |
| US3915709A (en) * | 1973-04-13 | 1975-10-28 | Gaf Corp | Backwetting coating for diazo microfilm |
| US4508808A (en) * | 1982-11-12 | 1985-04-02 | Xidex Corporation | Method of using diazotype photographic materials with preexposure treatment to form uniform sites of refractive index change |
Also Published As
| Publication number | Publication date |
|---|---|
| GB625999A (en) | 1949-07-07 |
| CH267973A (fr) | 1950-04-30 |
| FR947487A (fr) | 1949-07-04 |
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