US2871119A - Diazotype reproduction material and method - Google Patents
Diazotype reproduction material and method Download PDFInfo
- Publication number
- US2871119A US2871119A US489440A US48944055A US2871119A US 2871119 A US2871119 A US 2871119A US 489440 A US489440 A US 489440A US 48944055 A US48944055 A US 48944055A US 2871119 A US2871119 A US 2871119A
- Authority
- US
- United States
- Prior art keywords
- aluminum
- diazo
- light
- sensitive
- diazotype
- 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
- 239000000463 material Substances 0.000 title description 26
- 238000000034 method Methods 0.000 title description 18
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 34
- 229910052782 aluminium Inorganic materials 0.000 claims description 32
- 150000008049 diazo compounds Chemical class 0.000 claims description 23
- 229920001800 Shellac Polymers 0.000 claims description 14
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 claims description 14
- 239000004208 shellac Substances 0.000 claims description 14
- 229940113147 shellac Drugs 0.000 claims description 14
- 235000013874 shellac Nutrition 0.000 claims description 14
- 229920001220 nitrocellulos Polymers 0.000 claims description 12
- 239000001856 Ethyl cellulose Substances 0.000 claims description 11
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 11
- 229920001249 ethyl cellulose Polymers 0.000 claims description 11
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 11
- 239000000020 Nitrocellulose Substances 0.000 claims description 10
- 230000001464 adherent effect Effects 0.000 claims description 7
- 239000000203 mixture Substances 0.000 description 21
- 239000000243 solution Substances 0.000 description 21
- -1 particularly Chemical compound 0.000 description 16
- 239000002904 solvent Substances 0.000 description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 230000001235 sensitizing effect Effects 0.000 description 12
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 11
- 239000003960 organic solvent Substances 0.000 description 11
- 229920002678 cellulose Polymers 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 229910021529 ammonia Inorganic materials 0.000 description 6
- YKYOUMDCQGMQQO-UHFFFAOYSA-L cadmium dichloride Chemical compound Cl[Cd]Cl YKYOUMDCQGMQQO-UHFFFAOYSA-L 0.000 description 6
- 229920003086 cellulose ether Polymers 0.000 description 6
- 230000008878 coupling Effects 0.000 description 6
- 238000010168 coupling process Methods 0.000 description 6
- 238000005859 coupling reaction Methods 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 235000005074 zinc chloride Nutrition 0.000 description 5
- 239000011592 zinc chloride Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 241000238370 Sepia Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 3
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 3
- 239000011230 binding agent Substances 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
- 150000002148 esters Chemical class 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 3
- 229960001553 phloroglucinol Drugs 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000001119 stannous chloride Substances 0.000 description 3
- 235000011150 stannous chloride Nutrition 0.000 description 3
- 229910015900 BF3 Inorganic materials 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 2
- 239000011356 non-aqueous organic solvent Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000012260 resinous material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- IPRCBIWIPMJXIK-UHFFFAOYSA-N (3-hydroxyphenyl)urea Chemical compound NC(=O)NC1=CC=CC(O)=C1 IPRCBIWIPMJXIK-UHFFFAOYSA-N 0.000 description 1
- BPHYZRNTQNPLFI-UHFFFAOYSA-N 2,4,6-trihydroxytoluene Chemical compound CC1=C(O)C=C(O)C=C1O BPHYZRNTQNPLFI-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical class CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- ASHGTJPOSUFTGB-UHFFFAOYSA-N 3-methoxyphenol Chemical compound COC1=CC=CC(O)=C1 ASHGTJPOSUFTGB-UHFFFAOYSA-N 0.000 description 1
- GRLQBYQELUWBIO-UHFFFAOYSA-N 4,6-dichlorobenzene-1,3-diol Chemical compound OC1=CC(O)=C(Cl)C=C1Cl GRLQBYQELUWBIO-UHFFFAOYSA-N 0.000 description 1
- APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 description 1
- PDOWFCQCABIGHA-UHFFFAOYSA-N 4-n-ethoxybenzene-1,4-diamine Chemical compound CCONC1=CC=C(N)C=C1 PDOWFCQCABIGHA-UHFFFAOYSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 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
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-ethyl-N-phenylamine Natural products CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 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
- DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 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
- 125000003277 amino group Chemical group 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- OXAUNDBQHKIUSD-UHFFFAOYSA-N azanium;titanium;fluoride Chemical compound [NH4+].[F-].[Ti] OXAUNDBQHKIUSD-UHFFFAOYSA-N 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 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
- 230000001680 brushing effect Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 229960004279 formaldehyde Drugs 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- CDHZKUXAJKKENV-UHFFFAOYSA-N n-(2,5-dibutoxy-4-diazocyclohexa-1,5-dien-1-yl)benzamide Chemical compound C1=C(OCCCC)C(=[N+]=[N-])CC(OCCCC)=C1NC(=O)C1=CC=CC=C1 CDHZKUXAJKKENV-UHFFFAOYSA-N 0.000 description 1
- VDUQSXJYBDIGFR-UHFFFAOYSA-N n-benzyl-4-diazo-n-ethylcyclohexa-1,5-dien-1-amine Chemical compound C=1CC(=[N+]=[N-])C=CC=1N(CC)CC1=CC=CC=C1 VDUQSXJYBDIGFR-UHFFFAOYSA-N 0.000 description 1
- FLCPERRDPXWFDK-UHFFFAOYSA-N n-cyclohexyl-3-oxobutanamide Chemical compound CC(=O)CC(=O)NC1CCCCC1 FLCPERRDPXWFDK-UHFFFAOYSA-N 0.000 description 1
- ZPBSAMLXSQCSOX-UHFFFAOYSA-N naphthalene-1,3,6-trisulfonic acid Chemical compound OS(=O)(=O)C1=CC(S(O)(=O)=O)=CC2=CC(S(=O)(=O)O)=CC=C21 ZPBSAMLXSQCSOX-UHFFFAOYSA-N 0.000 description 1
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-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
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000012261 resinous substance Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229960004029 silicic acid Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/77—Photosensitive materials characterised by the base or auxiliary layers the base being of metal
-
- 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
- G03C1/60—Compositions containing diazo compounds as photosensitive substances with macromolecular additives
Definitions
- This invention relates to a diazotype reproduction material and method of manufacture. More particularly, it relates to the provision of a light-sensitive diazotype layer on a metal surface.
- an absorbent surface is commonly treated with a solution of lightsensitive components which serve to reproduce a desired image.
- diazotype reproduction media are produced by treating an absorbent surface with a solution containing azo dye components in an uncombined form.
- the most commonly used base material is paper, and the components are usually in aqueous solution. Sufiicient penetration is obtained to insure bonding of the paper and the sensitizing composition, and the ultimate dye image.
- Cellulose esters and ethers are also in common use as base materials, and they are impregnated with a sensitizing solution by the addition of penetrating or swelling agents which have a solvent action on the base material, to insure the necessary bonding.
- a particular object is to provide a reproduction material which includes an aluminum base and a light-sensitive diazotype layer thereon.
- a further object is to provide a diazotype reproduction element which furnishes excellent uniform permanent reproduction and which is resistant to the various conditions encountered.
- An additional object is to supply a reliable and effective method for providing a light-sensitive diazotype layer on an impervious aluminum surface, which surface absorbs substantially no water or organic solvent, so that it is unreceptive to aqueous and organic solvent solutions, for all practical purposes, and there will be no or only in- 2 substantial adherence or binding of the solutions and their ingredients to the surface.
- Another object is to coat analuminum base or support employing a principally non-aqueous organic solvent solution of a light-sensitive diazo compound.
- Still another object is to provide a base of aluminum sheet material and the like, and a strongly adherent diazotype layer thereon, whichmay be exposed to light under a drawing or pattern to mark the base rapidly and accurately for cutting or shaping into a template, pattern, structural part and the like.
- An additional object is to provide a method of preparing an aluminum body having a design on its surface.
- Yet another object is to provide a diazotype coat on an aluminum base material having the desired properties of transparency or translucency, little color, storage stability and resistance to chemical and physical attack under the conditions normally encountered.
- the invention provides a photographic reproduction material which includes an aluminum base material, and a coat of a light-sensitive diazo compound and a cellulose ester or ether, particularly, nitrocellulose or ethyl cellulose.
- a method for providing a diazotype layer on an aluminum surface includes coating the aluminum surface with an organic solvent solution of a diazo compound and the cellulose derivative.
- the wet coat is dried to provide a light-sensitive surface on the body, the light-sensitive surface is exposed to light of varying intensity, and the resulting print is developed to produce an aluminum body having a design on its surface.
- the aluminum surface is rendered receptive to the sensitizing composition by pitting or roughening, so that the surface is covered with a multitude of closely spaced fine pits, cavities or indentations.
- the surface is pitted by anodizing, alodyning, Diversey etching, or sand blasting, for example.
- the aluminum surface thus rendered receptive to the sensitizing composition is provided with an outer layer or coating of a light-sensitive diazo compound and ethyl cellulose or nitrocellulose, by applying the components in an organic solvent solution. Adherence to the surface is improved when the solution, and thus the result, ing coat, additionally contains a resinous material of the shellac type. Development of the subsequent print is also benefitted thereby.
- the films of the cellulose derivatives are not alone pervious to ammonia and water vapor, and to the developing solutions, so that a diazo layer cannot be overcoated satisfactorily with them, the thin films are sufliciently pervious when mixed with the diazo components to exhibit good developing properties.
- the films or coats may be regarded as water resistant and have excellent stability 'to heat, ammonia, water and water vapor, not swelling, loosening or dissolving,
- Diazo compounds which are organic solvent soluble and suitable for the sensitizing compositions of the invention include, for example, those which are derived from aromatic p-diamines of the benzene series, particularly a those which are N-mono or di-substituted on the undiazotized amino groups, with or without aliphatic substitution on the benzene ring. Also included are resinous condensation products of aldehydes, such as formaldehyde, with these light-sensitive diazo compounds, the p-amino phenyl sulfones of the diazo compounds.
- soluble diazo compounds are included.
- Specific examples of such compounds which are used in the production of diazetype images of high contrast are the diazo derivatives of p-amino-N-methyl aniline, p-arnino-N-di-methyl aniline, p-amino N ethyl aniline, p-amino-N-di-ethyl aniline, p-amino N methyl-N-ethyl aniline, p-amino-N-ethoxy aniline, p-amino-N-methyl-N-ethoxy aniline, pamino-N- ethyl-N-ethoxy aniline, p-amino-N-diethyl m toluio'ine, and l-amino-3-methyl-4-ethylamino benzene, all in the form of their diazodouble salts with zinc chloride, cadmium chloride, stannous chloride, or boron trifluoride
- any compound which will function as a coupling component may be employed either in the coating composition together with the diazo compound in order to produce a two-component system, or in the developing solution as a color forming developer.
- the coupling component selected will be one which will produce the desired color or a combination of coupling components which will produce a multi-color effect.
- Examples of preferred coupling components are: 2,3-dihydroxy naphthalene and its 6-sulfonic acid derivative, phloroglucinol, methyl phloro-glucinol, resorcinol, resorcinol-monomethyl ether, di-chloro resorcinol, m-hydroxy phenyl urea, acetoacetanilide, acetoacetylcyclohexyl amide, 7-hydroxy naphthalene-1-biguanide, 7-hydroxy-1,2-naphthimidazole, 2-amino-8-naphthol-3,6-disulfonic acid, 2-, 7-dihydroxy naphthalene, l-naphtholl-sulfonic acid, and 1-amino-8-naphthol-3,6-disulfonic acid.
- the sensitizing compositions may contain the usual adjuncts such as metal salts, to intensify the dyestutf image, i. e., aluminum sulfate, titanium ammonium fluoride, nickel sulfate and the like, and acids designed to retard precoupling such as citric acid, maleic acid, tartaric acid, boric acid and the like.
- adjuncts such as metal salts, to intensify the dyestutf image, i. e., aluminum sulfate, titanium ammonium fluoride, nickel sulfate and the like
- acids designed to retard precoupling such as citric acid, maleic acid, tartaric acid, boric acid and the like.
- the diazo composition can also advantageously include a filler such as colloidal silica, hydrated silica, diatomaceous earth, bentonite, mica and the like.
- a filler such as colloidal silica, hydrated silica, diatomaceous earth, bentonite, mica and the like.
- the filler acts to raise the softening point of the coating, promote development of a print by inducing porosity, and provide a mat surface.
- the sensitizing composition is a principally non-aqueous organic solvent solution of the diazo ingredients and the cellulose ester or ether, and preferably, a shellac type resinous material. tual compatibility and the properties desired.
- the solvent and film-forming ingredients are selected for solu- 'bility and are adjusted to a viscosity suitable for appli cation and which will properly suspend the filler, and to provide a continuous abrasion-resistant film.
- the solvents are preferably selected from the group of lower aliphatic alcohols, lower aliphatic ketones, lower aliphatic glycol esters and lower aliphatic glycol ethers, and they are specially selected to furnish a controlled rate of drying on application to the base material.
- the solvents are balanced to result in a drying rate which is slow enough to avoid condensation or pick-up of Water and to avoid premature drying in the rollers or other equipment, yet rapid enough to dry rapidly and completely in a satis factory manner after application, furnishing a thin uniform strongly adhering and non-tacky surface coat.
- a drying rate of -l0 minutes at l50l75 F. in commercial coating equipment is provided.
- the primary solvent for the mixture is methanol or ethanol, or acetone or methyl ethyl ketone may be sub-
- the ingredients are balanced for mustituted in whole or in part.
- the primary solvent is pres ent in a major proportion by weight of the total of'the" organic solvents, preferably -in a proportion of 60-90% of the solvents.
- the primary solvent is blended with a minor proportion, preferably 10-40%, of a higher boiling alcohol or the equivalent, which serves to prevent overly rapid drying with consequent blushing.
- the medium boiling lower aliphatic alcohols having 4 carbon atoms or more and which are; liquid at room temperature, such as butyl alcohol and amyl alcohol, are desirably employed, and they may be substituted in whole or in part by lower aliphatic glycol esters or ethers, such as the esters or ethers of ethylene glycol, propylene glycol and glycerine.
- lower aliphatic glycol esters or ethers such as the esters or ethers of ethylene glycol, propylene glycol and glycerine.
- normal or, isopropanol may be used alone.
- a preferred combination of solvents is a mixture of -85% of methanol and 10-15% of butanol, or an equivalent mixture.
- compositions which are ammonia developed after printing a small amount of a loweraliphatic glycol; such as ethylene glycol, propylene glycol and glycerine, may be included to assist in picking up water vapor in developing.
- a loweraliphatic glycol such as ethylene glycol, propylene glycol and glycerine
- the proportion ofglycol is preferably about Mr to 1 part by weight to 1 part of the cellulose derivative.
- Cellosolve esters such as the lower aliphatic Cellosolve esters, preferably B-alkoxy ethyl acetate.
- the cellulose ether or ester binder is preferably employed in a proportion of about A to. 5 parts by weight to l partof diazo compound.
- the reference to diazocompound does not include the coupling components and the-adjuncts.
- a shellac type resinous substance is included-in a proportion of about A tol part by weight'to 1 part of cellulose ether or ester.
- solvent-per part of the cellulose binder About 30 to 60 parts by weight of solvent-per part of the cellulose binder are employed, equivalent to apropcrtion of binder of about 3.3% to 1.6% based on the solvents. About 20 to 200 parts by weight of solvent are employedper-part ofdiazo compound, so'that'the' diazo compound is-present in a proportion of about '5 to 0.5% of the solvents. It is ordinarilypreferred to ilIL-- corporate about 0.5 to 5 parts of filler per part of diazocompound.
- the composition includes merely'sulficient water todissolve those components of the diazo system'which are insoluble or difficultly soluble inorganic solvents, but. not enough to preicpitate the cellulose ester or ether or"- the shellac, and -the proportion-of waterthusamountsto a maximum of about 3% by weightof the complete.-
- the sensitizing composition prepared in the above manner is applied to the receptive aluminum surfaceby brushing, spraying, bead-coating, roller coating,-- silk screening, or the like, to provide a thin'coat onthe surface. of from about room temperature to'about- 250- F, the upper temperature being limited by the stability of the diazo components.
- An adherent sensitized layer is thus firmly bonded to the aluminum surface.
- the reproduction material so produced can be exposed to light'of varying intensity in accordance with a design to be reproduced thereon, e.
- the finaldiazctype reproduction on the aluminum surface will be an exact true-to-scale duplicate copy of the original.
- the resulting copy is unaffected by atmosphericmoistureand requires no over-spraying or
- the material is dried in the dark, at a temperaturelacquering, as there is no rubbing or peelingofi' of the surface, and the image is well protected.
- the sensitized aluminum materials and the resulting prints may be transported and employed in various localities; for example, they have found widespread application in the manufacture of metal templates in the aircraft industry.
- Example The example illustrates production of a direct (positive image) dimensionally stable blue line print, ammonia developed, on an aluminum metal sheet.
- the solution is prepared, having the following compositions:
- An aluminum metal sheet, deep-etched (anodized), 12 long, 4' wide, and 0.125" thick, represented by the numeral 1 in the drawing, is uniformly spray coated in a layer about 00001-00002" thick with the above-described sensitizing solution, and dried in the dark, so that a coat or film 2 is provided on a surface of the sheet and strongly adheres thereto.
- a print is made on the sensitized metal sheet, using as the original pattern, a 12' x 4 sepia intermediate print on plastic-impregnated glass cloth.
- the metal plate is contact printed by means of an are light, and is developed by placing it in a wooden box, 14 long, 5' high, and 1' wide, filled with ammonia and Water vapors.
- the resulting blue-line positive copy is an exact, trueto-scale, positive reproduction of the sepia intermediate print, having a very small distortion.
- the above mix may also include 100 cc. of ethylene glycol or propylene glycol, to assist in developing.
- 200 gms. of ethyl cellulose (Hercules N-SO) can be employed.
- Two-component diazo systems can be substituted such as p-diazo-N-methyl-N-hydroxy-ethyl aniline, zinc chloride double salt, and resorcinol, which produces a direct sepia print; and p-diazo-N-ethyl-N-ethoxy aniline, stannous chloride double salt, and 2,3-di-hydroxynaphthalene, which produces a direct blue line print.
- a one-component diazo system can also be employed, such as p-diazo-N-ethyl-N-benzyl aniline, cadmium chloride double salt, and naphthalene-1,3,6-tri-sulfonic acid, sodium salt, developed with phloroglucinol and resorcinol solution, which produces a direct sepia line print; and 4- diazo-N-benzoyl-2,5-dibutoxy aniline, zinc chloride double salt, developed with phloroglucinol solution, which produces a direct black line print.
- Other combinations of light-sensitive diazo compounds, or light-sensitive diazo visually reproducing a drawing on exposure to light and developing by undergoing a substantial color change, can be substituted for the compounds employed.
- a new and improved photographic reproduction material constituting a sensitized aluminum base is provided.
- This material is especially useful for rapidly and accurately reproducing a drawing or pattern on the surface of the aluminum, for producing templates, structural members and the like.
- Aluminum sheets may be coated simply and rapidly at any location, transported as desired and exposed under a drawing suited for the intended purpose. The method and material find especially advantageous use in quantity production.
- An aluminum base and an adherent coat of a lightsensitive diazo compound a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac.
- a pitted aluminum sheet and an adherent coat of a light-sensitive diazo compound a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac.
- the method for providing a light-sensitive diazotype layer on an aluminum surface which comprises coating said surfacewith an organic solvent solution of a light-sensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac.
- the method for providing a light-sensitive diazotype layer on an aluminum surface which comprises coating said surface with an organic solvent solution of a light-sensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac, said solvent being selected from the class consisting of lower aliphatic alcohols, lower aliphatic ketones, lower aliphatic glycol esters, and lower aliphatic glycol ethers.
- the method for providing a light-sensitive diazotype layer on an aluminum surface which comprises coating said surface with an organic solvent solution of a lightsensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac, said solvent being a mixture of methanol and butanol.
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Description
Jan. 1959 R. P. WEEGAR ET AL 2,
DIAZOTYPE REPRODUCTION MATERIAL AND METHOD Filed Feb. 21, 1955 Coat of Lightsensirive Dmzo Compound,
Anodized Aluminun Sh eet c m M h S d INVENTORS'. RALPH P WEEGAR HENRY C. UNKAUF ATT'YS 2,871,119 Patented Jan. 27, 1959 DIAZOTYPE REPRODUCTION MATERIAL AND METHOD Ralph P. Weegar, Villa Park, and Henry 'C. Unkauf, Chicage, 11]., assignors to Eugene Diet'zgen C0,, Chicago, 111., a corporation of Delaware Application February 21, 1955, Serial No. 489,440
8 Claims. (CI. 96-49) This invention relates to a diazotype reproduction material and method of manufacture. More particularly, it relates to the provision of a light-sensitive diazotype layer on a metal surface.
Water and organic solvent-impervious metal surfaces pose difiicult problems in the application and fixation thereon of materials which provide photographic lightsensitive layers. In the provision of photographic lightsensitive layers on other base materials, an absorbent surface is commonly treated with a solution of lightsensitive components which serve to reproduce a desired image. Thus, for example, diazotype reproduction media are produced by treating an absorbent surface with a solution containing azo dye components in an uncombined form. The most commonly used base material is paper, and the components are usually in aqueous solution. Sufiicient penetration is obtained to insure bonding of the paper and the sensitizing composition, and the ultimate dye image. Cellulose esters and ethers are also in common use as base materials, and they are impregnated with a sensitizing solution by the addition of penetrating or swelling agents which have a solvent action on the base material, to insure the necessary bonding.
The prior methods are, however, unsuitable for coating liquid-impervious metal surfaces, there being insuflicient bonding with the base material to provide a uniform layer of the sensitizing components which is permanently bonded and is resistant to wear and abrasion. Furthermore, the dye images reproduced on the surface by exposure and development have little permanency, and in order to prevent easy removal of the images, it is necessary to overcoat them with a transparent coating. Even such a coating on a metal is easily scratched, chipped and otherwise damaged in ordinary handling, shipping, and storage.
There are a number of advantages in the use of dimensionally stable aluminum base materials, especially in the production of aluminum templates or the like, and
it is highly desirable to provide an aluminum base coated with a light-sensitive layer.
It is therefore an object of the invention to provide a new and improved diazotype reproduction material and method of manufacture, particularly a dimensionally stable photographic reproduction material.
A particular object is to provide a reproduction material which includes an aluminum base and a light-sensitive diazotype layer thereon.
A further object is to provide a diazotype reproduction element which furnishes excellent uniform permanent reproduction and which is resistant to the various conditions encountered.
An additional object is to supply a reliable and effective method for providing a light-sensitive diazotype layer on an impervious aluminum surface, which surface absorbs substantially no water or organic solvent, so that it is unreceptive to aqueous and organic solvent solutions, for all practical purposes, and there will be no or only in- 2 substantial adherence or binding of the solutions and their ingredients to the surface.
Another object is to coat analuminum base or support employing a principally non-aqueous organic solvent solution of a light-sensitive diazo compound.
Still another object is to provide a base of aluminum sheet material and the like, and a strongly adherent diazotype layer thereon, whichmay be exposed to light under a drawing or pattern to mark the base rapidly and accurately for cutting or shaping into a template, pattern, structural part and the like.
An additional object is to provide a method of preparing an aluminum body having a design on its surface.
Yet another object is to provide a diazotype coat on an aluminum base material having the desired properties of transparency or translucency, little color, storage stability and resistance to chemical and physical attack under the conditions normally encountered.
Other objects include the manufacture and application of new and improved coating compositions, and coats and coated base materials, and the provision of new and useful methods. These and other objects and advantages of the invention will appear on consideration of the specification taken in conjunction with the attached drawing, in which the single figure is a broken perspective view of a sheet of anodized aluminum provided with a diazotype layer or coat, according to a preferred embodiment of the invention.
The invention provides a photographic reproduction material which includes an aluminum base material, and a coat of a light-sensitive diazo compound and a cellulose ester or ether, particularly, nitrocellulose or ethyl cellulose.
A method for providing a diazotype layer on an aluminum surface is provided in the invention, which method includes coating the aluminum surface with an organic solvent solution of a diazo compound and the cellulose derivative. The wet coat is dried to provide a light-sensitive surface on the body, the light-sensitive surface is exposed to light of varying intensity, and the resulting print is developed to produce an aluminum body having a design on its surface.
The aluminum surface is rendered receptive to the sensitizing composition by pitting or roughening, so that the surface is covered with a multitude of closely spaced fine pits, cavities or indentations. The surface is pitted by anodizing, alodyning, Diversey etching, or sand blasting, for example.
The aluminum surface thus rendered receptive to the sensitizing composition is provided with an outer layer or coating of a light-sensitive diazo compound and ethyl cellulose or nitrocellulose, by applying the components in an organic solvent solution. Adherence to the surface is improved when the solution, and thus the result, ing coat, additionally contains a resinous material of the shellac type. Development of the subsequent print is also benefitted thereby.
An important phenomenon cooperating in the invention is that although the films of the cellulose derivatives are not alone pervious to ammonia and water vapor, and to the developing solutions, so that a diazo layer cannot be overcoated satisfactorily with them, the thin films are sufliciently pervious when mixed with the diazo components to exhibit good developing properties. On the other hand, the films or coats may be regarded as water resistant and have excellent stability 'to heat, ammonia, water and water vapor, not swelling, loosening or dissolving,
"and they are very rugged and durable.
Diazo compounds which are organic solvent soluble and suitable for the sensitizing compositions of the invention include, for example, those which are derived from aromatic p-diamines of the benzene series, particularly a those which are N-mono or di-substituted on the undiazotized amino groups, with or without aliphatic substitution on the benzene ring. Also included are resinous condensation products of aldehydes, such as formaldehyde, with these light-sensitive diazo compounds, the p-amino phenyl sulfones of the diazo compounds. The boron trifluoride, the stannous chloride, the cadmium chloride, and the zinc chloride double salts of the aforementioned light sensitive organic solvent. soluble diazo compounds are included. Specific examples ofsuch compounds which are used in the production of diazetype images of high contrast are the diazo derivatives of p-amino-N-methyl aniline, p-arnino-N-di-methyl aniline, p-amino N ethyl aniline, p-amino-N-di-ethyl aniline, p-amino N methyl-N-ethyl aniline, p-amino-N-ethoxy aniline, p-amino-N-methyl-N-ethoxy aniline, pamino-N- ethyl-N-ethoxy aniline, p-amino-N-diethyl m toluio'ine, and l-amino-3-methyl-4-ethylamino benzene, all in the form of their diazodouble salts with zinc chloride, cadmium chloride, stannous chloride, or boron trifluoride, or their diazo p-amino-phenyl sulfones, or their diazo-form aldehyde resinous condensation products.
As coupling components, any compound which will function as a coupling component may be employed either in the coating composition together with the diazo compound in order to produce a two-component system, or in the developing solution as a color forming developer. In either case, the coupling component selected will be one which will produce the desired color or a combination of coupling components which will produce a multi-color effect. Examples of preferred coupling components are: 2,3-dihydroxy naphthalene and its 6-sulfonic acid derivative, phloroglucinol, methyl phloro-glucinol, resorcinol, resorcinol-monomethyl ether, di-chloro resorcinol, m-hydroxy phenyl urea, acetoacetanilide, acetoacetylcyclohexyl amide, 7-hydroxy naphthalene-1-biguanide, 7-hydroxy-1,2-naphthimidazole, 2-amino-8-naphthol-3,6-disulfonic acid, 2-, 7-dihydroxy naphthalene, l-naphtholl-sulfonic acid, and 1-amino-8-naphthol-3,6-disulfonic acid.
The sensitizing compositions may contain the usual adjuncts such as metal salts, to intensify the dyestutf image, i. e., aluminum sulfate, titanium ammonium fluoride, nickel sulfate and the like, and acids designed to retard precoupling such as citric acid, maleic acid, tartaric acid, boric acid and the like.
The diazo composition can also advantageously include a filler such as colloidal silica, hydrated silica, diatomaceous earth, bentonite, mica and the like. The filler acts to raise the softening point of the coating, promote development of a print by inducing porosity, and provide a mat surface.
The sensitizing composition is a principally non-aqueous organic solvent solution of the diazo ingredients and the cellulose ester or ether, and preferably, a shellac type resinous material. tual compatibility and the properties desired. The solvent and film-forming ingredients are selected for solu- 'bility and are adjusted to a viscosity suitable for appli cation and which will properly suspend the filler, and to provide a continuous abrasion-resistant film. The solvents are preferably selected from the group of lower aliphatic alcohols, lower aliphatic ketones, lower aliphatic glycol esters and lower aliphatic glycol ethers, and they are specially selected to furnish a controlled rate of drying on application to the base material. Thus, the solvents are balanced to result in a drying rate which is slow enough to avoid condensation or pick-up of Water and to avoid premature drying in the rollers or other equipment, yet rapid enough to dry rapidly and completely in a satis factory manner after application, furnishing a thin uniform strongly adhering and non-tacky surface coat. For example, a drying rate of -l0 minutes at l50l75 F. in commercial coating equipment is provided.
The primary solvent for the mixture is methanol or ethanol, or acetone or methyl ethyl ketone may be sub- The ingredients are balanced for mustituted in whole or in part. The primary solvent is pres ent in a major proportion by weight of the total of'the" organic solvents, preferably -in a proportion of 60-90% of the solvents. The primary solvent is blended with a minor proportion, preferably 10-40%, of a higher boiling alcohol or the equivalent, which serves to prevent overly rapid drying with consequent blushing. The medium boiling lower aliphatic alcohols having 4 carbon atoms or more and which are; liquid at room temperature, such as butyl alcohol and amyl alcohol, are desirably employed, and they may be substituted in whole or in part by lower aliphatic glycol esters or ethers, such as the esters or ethers of ethylene glycol, propylene glycol and glycerine. In a controlled low humidity, normal or, isopropanol may be used alone.
A preferred combination of solvents is a mixture of -85% of methanol and 10-15% of butanol, or an equivalent mixture.
In the compositions which are ammonia developed after printing, a small amount of a loweraliphatic glycol; such as ethylene glycol, propylene glycol and glycerine, may be included to assist in picking up water vapor in developing. The proportion ofglycol is preferably about Mr to 1 part by weight to 1 part of the cellulose derivative.
This function together with that of the secondary or higherboiling solvent is also provided by Cellosolve esters, such as the lower aliphatic Cellosolve esters, preferably B-alkoxy ethyl acetate.
in the sensitizing composition, the cellulose ether or ester binder ispreferably employed in a proportion of about A to. 5 parts by weight to l partof diazo compound. The reference to diazocompound does not include the coupling components and the-adjuncts. Preferably, a shellac type resinous substance is included-in a proportion of about A tol part by weight'to 1 part of cellulose ether or ester.
About 30 to 60 parts by weight of solvent-per part of the cellulose binder are employed, equivalent to apropcrtion of binder of about 3.3% to 1.6% based on the solvents. About 20 to 200 parts by weight of solvent are employedper-part ofdiazo compound, so'that'the' diazo compound is-present in a proportion of about '5 to 0.5% of the solvents. It is ordinarilypreferred to ilIL-- corporate about 0.5 to 5 parts of filler per part of diazocompound.
The composition includes merely'sulficient water todissolve those components of the diazo system'which are insoluble or difficultly soluble inorganic solvents, but. not enough to preicpitate the cellulose ester or ether or"- the shellac, and -the proportion-of waterthusamountsto a maximum of about 3% by weightof the complete.-
sensitizing composition.
The sensitizing composition prepared in the above manner is applied to the receptive aluminum surfaceby brushing, spraying, bead-coating, roller coating,-- silk screening, or the like, to providea thin'coat onthe surface. of from about room temperature to'about- 250- F, the upper temperature being limited by the stability of the diazo components. An adherent sensitized layer is thus firmly bonded to the aluminum surface. The reproduction material so produced can be exposed to light'of varying intensity in accordance with a design to be reproduced thereon, e. g., under a pattern to be reproduced, and the images developed by exposure to ammonia vapors inthe case of the two-component or dry-developing process, or by spraying, dipping, swabbing or sponging witha developing solution in the case of the one-componentor moist-developing process.
When the original pattern or drawing is produced on a dimensionally .stable medium, such as photo-template glass cloth, the finaldiazctype reproduction on the aluminum surface will be an exact true-to-scale duplicate copy of the original. The resulting copy is unaffected by atmosphericmoistureand requires no over-spraying or The material is dried in the dark, at a temperaturelacquering, as there is no rubbing or peelingofi' of the surface, and the image is well protected. The sensitized aluminum materials and the resulting prints may be transported and employed in various localities; for example, they have found widespread application in the manufacture of metal templates in the aircraft industry.
The following example is furnished to assist in providing a complete understanding of the invention, but it is to be understood that the invention is not limited thereto nor to the specific compositions, proportions and conditions set forth therein, which are given only for purposes of illustration.
Example The example illustrates production of a direct (positive image) dimensionally stable blue line print, ammonia developed, on an aluminum metal sheet.
The solution is prepared, having the following compositions:
p Diazo N diethyl m toluidine, zinc chloride double salt ms 5 5 These ingredients, thoroughly mixed and filtered, are added to the following mixture:
Methanol cc 3,500 n-Butanol cc 500 Shellac (bleached, dewaxed) gms 100 Nitrocotton (RS 5-6 sec.) gms 200 Diatomaceous earth (Johns-Manville Celite) gms-- 75 The final mix is stored in a covered crock until ready for use.
An aluminum metal sheet, deep-etched (anodized), 12 long, 4' wide, and 0.125" thick, represented by the numeral 1 in the drawing, is uniformly spray coated in a layer about 00001-00002" thick with the above-described sensitizing solution, and dried in the dark, so that a coat or film 2 is provided on a surface of the sheet and strongly adheres thereto. A print is made on the sensitized metal sheet, using as the original pattern, a 12' x 4 sepia intermediate print on plastic-impregnated glass cloth. The metal plate is contact printed by means of an are light, and is developed by placing it in a wooden box, 14 long, 5' high, and 1' wide, filled with ammonia and Water vapors.
The resulting blue-line positive copy is an exact, trueto-scale, positive reproduction of the sepia intermediate print, having a very small distortion.
The above mix may also include 100 cc. of ethylene glycol or propylene glycol, to assist in developing. In place of the nitrocotton, 200 gms. of ethyl cellulose (Hercules N-SO) can be employed.
Other two-component diazo systems can be substituted such as p-diazo-N-methyl-N-hydroxy-ethyl aniline, zinc chloride double salt, and resorcinol, which produces a direct sepia print; and p-diazo-N-ethyl-N-ethoxy aniline, stannous chloride double salt, and 2,3-di-hydroxynaphthalene, which produces a direct blue line print. A one-component diazo system can also be employed, such as p-diazo-N-ethyl-N-benzyl aniline, cadmium chloride double salt, and naphthalene-1,3,6-tri-sulfonic acid, sodium salt, developed with phloroglucinol and resorcinol solution, which produces a direct sepia line print; and 4- diazo-N-benzoyl-2,5-dibutoxy aniline, zinc chloride double salt, developed with phloroglucinol solution, which produces a direct black line print. Other combinations of light-sensitive diazo compounds, or light-sensitive diazo visually reproducing a drawing on exposure to light and developing by undergoing a substantial color change, can be substituted for the compounds employed.
In this manner, a new and improved photographic reproduction material constituting a sensitized aluminum base is provided. This material is especially useful for rapidly and accurately reproducing a drawing or pattern on the surface of the aluminum, for producing templates, structural members and the like. Aluminum sheets may be coated simply and rapidly at any location, transported as desired and exposed under a drawing suited for the intended purpose. The method and material find especially advantageous use in quantity production.
What is claimed is:
1. An aluminum base and an adherent coat of a lightsensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac.
2. A pitted aluminum sheet and an adherent coat of a light-sensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac.
3. An aluminum base and an adherent coat of a lightsensitive diazo compound, ethyl cellulose, and shellac.
4. An aluminum base and an adherent coat of a lightsensitive diazo compound, nitrocellulose, and shellac.
5. The method for providing a light-sensitive diazotype layer on an aluminum surface which comprises coating said surfacewith an organic solvent solution of a light-sensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac.
6. The method for providing a light-sensitive diazotype layer on an aluminum surface which comprises coating said surface with an organic solvent solution of a light-sensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac, said solvent being selected from the class consisting of lower aliphatic alcohols, lower aliphatic ketones, lower aliphatic glycol esters, and lower aliphatic glycol ethers.
7. The method for providing a light-sensitive diazotype layer on an aluminum surface which comprises coating said surface with an organic solvent solution of a lightsensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac, said solvent being a mixture of methanol and butanol.
8. The method of preparing an aluminum body having a design on a surface thereof which comprises coating a pitted surface of an aluminum body with an organic solvent solution of a light-sensitive diazo compound, a member selected from the class consisting of ethyl cellulose and nitrocellulose, and shellac, drying the thus coated body, exposing the resulting light-sensitive surface of said body to light of varying intensity in accordance with a design to be reproduced, and developing the resulting print.
References Cited in the file of this patent UNITED STATES PATENTS Great Britain July 7, 1954
Claims (1)
1. AN ALUMINUM BASE AND AN ADHERENT COAT OF LIGHTSENSITIVE DIAZO COMPOUND, A MEMBER SELECTED FROM THE CLASS CONSISTING OF ETHYL CELLULOSE AND NITROCELLULOSE, AND SHELLAC.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US489440A US2871119A (en) | 1955-02-21 | 1955-02-21 | Diazotype reproduction material and method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US489440A US2871119A (en) | 1955-02-21 | 1955-02-21 | Diazotype reproduction material and method |
Publications (1)
Publication Number | Publication Date |
---|---|
US2871119A true US2871119A (en) | 1959-01-27 |
Family
ID=23943868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US489440A Expired - Lifetime US2871119A (en) | 1955-02-21 | 1955-02-21 | Diazotype reproduction material and method |
Country Status (1)
Country | Link |
---|---|
US (1) | US2871119A (en) |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3844908A (en) * | 1971-12-24 | 1974-10-29 | Dainichiseika Color Chem | Process for coloring aluminum and aluminum alloys |
US4153461A (en) * | 1967-12-04 | 1979-05-08 | Hoechst Aktiengesellschaft | Layer support for light-sensitive material adapted to be converted into a planographic printing plate |
US4172729A (en) * | 1976-06-28 | 1979-10-30 | Fuji Photo Film Co., Ltd. | Photosensitive diazo lithographic printing plate with oxalic acid as stabilizer |
US4198470A (en) * | 1975-06-09 | 1980-04-15 | Western Litho Plate & Supply Co. | Base plate and lithographic plate prepared by sensitization thereof |
US4205989A (en) * | 1976-04-14 | 1980-06-03 | Kimoto & Co., Ltd. | Dry system image producing element |
US4248959A (en) * | 1978-12-07 | 1981-02-03 | American Hoechst Corporation | Preparation of diazo printing plates using laser exposure |
US4272604A (en) * | 1975-06-09 | 1981-06-09 | Western Litho Plate & Supply Co. | Base plate and lithographic plate prepared by sensitization thereof |
US4272605A (en) * | 1975-06-09 | 1981-06-09 | Western Litho Plate & Supply Co. | Base plate and lithographic plate prepared by sensitization thereof |
US4288520A (en) * | 1978-08-03 | 1981-09-08 | Hoechst Aktiengesellschaft | Process of manufacturing light-sensitive copying material based on diazonium salt condensation products |
FR2489849A1 (en) * | 1980-09-08 | 1982-03-12 | Schenk Co | PROCESS FOR COLORING ALUMINUM OXIDE OR ALUMINUM ALLOY LAYERS USING ORGANIC COMPOUNDS |
US4446218A (en) * | 1982-03-18 | 1984-05-01 | American Hoechst Corporation | Sulfur and/or amide-containing exposure accelerators for light-sensitive coatings with diazonium compounds |
US4486529A (en) * | 1976-06-10 | 1984-12-04 | American Hoechst Corporation | Dialo printing plate made from laser |
US4499170A (en) * | 1983-06-17 | 1985-02-12 | Richardson Graphics Company | Lithographic plates and photoresists having stabilized photosensitive diazo resin with theophylline derivative |
US4522910A (en) * | 1975-06-19 | 1985-06-11 | Napp Systems (Usa), Inc. | Photosensitive graphic arts article |
US4533619A (en) * | 1982-03-18 | 1985-08-06 | American Hoechst Corporation | Acid stabilizers for diazonium compound condensation products |
US4687726A (en) * | 1984-05-12 | 1987-08-18 | Hoechst Aktiengesellschaft | Photosensitive recording material for use in the production of negative-working planographic printing plates with diazonium polycondensate and inorganic pigment |
US4783390A (en) * | 1983-08-01 | 1988-11-08 | Sanyo-Kokusaku Pulp Co., Ltd. | Multicolor diazo image-forming material |
US4937170A (en) * | 1982-11-19 | 1990-06-26 | Hoechst Celanese Corporation | Coupling agents for photographic elements |
US4950577A (en) * | 1984-06-11 | 1990-08-21 | Minnesota Mining And Manufacturing Company | Pre-press light-sensitive color proofing article incorporating antihalation layer |
US4980263A (en) * | 1988-03-03 | 1990-12-25 | Fuji Photo Film Co., Ltd. | Light-sensitive diazo resin composition with polyurethane and compound having ureido, thioureido, urethane, or thiourethane unit |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB539314A (en) * | 1939-04-11 | 1941-09-04 | Philips Nv | Improvements in or relating to layers sensitised by means of a diazonium compound and method of preparing such layers |
GB563804A (en) * | 1943-05-06 | 1944-08-30 | Hall Harding Ltd | Improvements relating to the production of diazotype prints |
US2409564A (en) * | 1941-05-28 | 1946-10-15 | Noc Mfg Company Di | Transfer material |
US2593928A (en) * | 1947-10-09 | 1952-04-22 | Gen Aniline & Film Corp | Dimensionally stable diazotype photographic film and process for making it |
GB711626A (en) * | 1950-10-31 | 1954-07-07 | Kalle & Co Ag | Improvements in processes and materials for photo-mechanical reproduction |
US2714066A (en) * | 1950-12-06 | 1955-07-26 | Minnesota Mining & Mfg | Planographic printing plate |
-
1955
- 1955-02-21 US US489440A patent/US2871119A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB539314A (en) * | 1939-04-11 | 1941-09-04 | Philips Nv | Improvements in or relating to layers sensitised by means of a diazonium compound and method of preparing such layers |
US2409564A (en) * | 1941-05-28 | 1946-10-15 | Noc Mfg Company Di | Transfer material |
GB563804A (en) * | 1943-05-06 | 1944-08-30 | Hall Harding Ltd | Improvements relating to the production of diazotype prints |
US2593928A (en) * | 1947-10-09 | 1952-04-22 | Gen Aniline & Film Corp | Dimensionally stable diazotype photographic film and process for making it |
GB711626A (en) * | 1950-10-31 | 1954-07-07 | Kalle & Co Ag | Improvements in processes and materials for photo-mechanical reproduction |
US2714066A (en) * | 1950-12-06 | 1955-07-26 | Minnesota Mining & Mfg | Planographic printing plate |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4153461A (en) * | 1967-12-04 | 1979-05-08 | Hoechst Aktiengesellschaft | Layer support for light-sensitive material adapted to be converted into a planographic printing plate |
US3844908A (en) * | 1971-12-24 | 1974-10-29 | Dainichiseika Color Chem | Process for coloring aluminum and aluminum alloys |
US4198470A (en) * | 1975-06-09 | 1980-04-15 | Western Litho Plate & Supply Co. | Base plate and lithographic plate prepared by sensitization thereof |
US4272604A (en) * | 1975-06-09 | 1981-06-09 | Western Litho Plate & Supply Co. | Base plate and lithographic plate prepared by sensitization thereof |
US4272605A (en) * | 1975-06-09 | 1981-06-09 | Western Litho Plate & Supply Co. | Base plate and lithographic plate prepared by sensitization thereof |
US4522910A (en) * | 1975-06-19 | 1985-06-11 | Napp Systems (Usa), Inc. | Photosensitive graphic arts article |
US4205989A (en) * | 1976-04-14 | 1980-06-03 | Kimoto & Co., Ltd. | Dry system image producing element |
US4486529A (en) * | 1976-06-10 | 1984-12-04 | American Hoechst Corporation | Dialo printing plate made from laser |
US4172729A (en) * | 1976-06-28 | 1979-10-30 | Fuji Photo Film Co., Ltd. | Photosensitive diazo lithographic printing plate with oxalic acid as stabilizer |
US4288520A (en) * | 1978-08-03 | 1981-09-08 | Hoechst Aktiengesellschaft | Process of manufacturing light-sensitive copying material based on diazonium salt condensation products |
US4248959A (en) * | 1978-12-07 | 1981-02-03 | American Hoechst Corporation | Preparation of diazo printing plates using laser exposure |
FR2489849A1 (en) * | 1980-09-08 | 1982-03-12 | Schenk Co | PROCESS FOR COLORING ALUMINUM OXIDE OR ALUMINUM ALLOY LAYERS USING ORGANIC COMPOUNDS |
US4446218A (en) * | 1982-03-18 | 1984-05-01 | American Hoechst Corporation | Sulfur and/or amide-containing exposure accelerators for light-sensitive coatings with diazonium compounds |
US4533619A (en) * | 1982-03-18 | 1985-08-06 | American Hoechst Corporation | Acid stabilizers for diazonium compound condensation products |
US4937170A (en) * | 1982-11-19 | 1990-06-26 | Hoechst Celanese Corporation | Coupling agents for photographic elements |
US4499170A (en) * | 1983-06-17 | 1985-02-12 | Richardson Graphics Company | Lithographic plates and photoresists having stabilized photosensitive diazo resin with theophylline derivative |
US4783390A (en) * | 1983-08-01 | 1988-11-08 | Sanyo-Kokusaku Pulp Co., Ltd. | Multicolor diazo image-forming material |
US4687726A (en) * | 1984-05-12 | 1987-08-18 | Hoechst Aktiengesellschaft | Photosensitive recording material for use in the production of negative-working planographic printing plates with diazonium polycondensate and inorganic pigment |
US4950577A (en) * | 1984-06-11 | 1990-08-21 | Minnesota Mining And Manufacturing Company | Pre-press light-sensitive color proofing article incorporating antihalation layer |
US4980263A (en) * | 1988-03-03 | 1990-12-25 | Fuji Photo Film Co., Ltd. | Light-sensitive diazo resin composition with polyurethane and compound having ureido, thioureido, urethane, or thiourethane unit |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2871119A (en) | Diazotype reproduction material and method | |
US3353984A (en) | Method for the preparation of lightsensitive diazotype materials and improved materials prepared by such method | |
US2528395A (en) | Diazotype dry strip film | |
US2848327A (en) | Glass fabric resin impregnated base coated with a light sensitive layer | |
US3027256A (en) | Production of light-sensitive diazotype materials | |
US2873207A (en) | Diazotype reproduction material and method | |
US3153592A (en) | Complex salt diazotype photoprinting materials | |
US2603564A (en) | Light sensitive diazotype layer containing a white opacifying pigment | |
US2531485A (en) | Diazotypes comprising amine salts of sulfonic acid containing azo components | |
US2772160A (en) | Light-detached resists or reliefs for printing plates | |
US2593839A (en) | Diazotype photoprinting material | |
US2773768A (en) | Light-sensitive diazotype material | |
US2532126A (en) | Diazotype photographic material | |
US2661291A (en) | Antidiffusion diazotypes having tetrazo diphenyls as the light sensitive agent | |
US2537106A (en) | Poly-acetoacetyl derivatives of polyamines as azo components in diazotype photoprinting material | |
US2632703A (en) | Light sensitive diazotype materials containing tetrazo diphenyl compounds | |
US2591309A (en) | Photographically sensitive diazotype element | |
US3169067A (en) | Heat developable diazotype material comprising an unsymmetrical urea as the base release agent | |
US3228769A (en) | Photosensitive copy-sheet comprising zinc oxide and a diazonium compound and method of copying | |
US3367776A (en) | Heat sensitive diazotype materials | |
US2542560A (en) | Diazotypes on plastic surfaced carrier containing 5,5' diresorcinol | |
US2593928A (en) | Dimensionally stable diazotype photographic film and process for making it | |
US3052542A (en) | Intermediate master for use in the diazotype process and a process for producing same | |
US3191030A (en) | Process of making and using thermographic reproduction paper | |
US2529464A (en) | Diazotype composition containing n-hydroxyethyl-m-toluidine-p-diazos |