NO773984L - Tokomponent-diazotypimaterial. - Google Patents

Tokomponent-diazotypimaterial.

Info

Publication number: NO773984L
Authority: NO; Norway
Prior art keywords: acidic groups; light; material according; acid; resin containing
Prior art date: 1976-11-22

Application number

NO773984A

Other languages

English (en)

Norwegian (no)

Inventor

Hans-Dieter Frommeld

Original Assignee

Hoechst Ag

Priority date (The priority date 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 date listed.)

1976-11-22

Filing date

1977-11-21

Publication date

1978-05-23

1977-11-21 Application filed by Hoechst Ag filed Critical Hoechst Ag

1978-05-23 Publication of NO773984L publication Critical patent/NO773984L/no

Links

229920005989 resin Polymers 0.000 claims description 19
239000011347 resin Substances 0.000 claims description 19
230000002378 acidificating effect Effects 0.000 claims description 15
239000000463 material Substances 0.000 claims description 13
239000002253 acid Substances 0.000 claims description 11
-1 alkyl vinyl ethers Chemical class 0.000 claims description 11
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 11
239000011888 foil Substances 0.000 claims description 10
230000002209 hydrophobic effect Effects 0.000 claims description 10
239000011230 binding agent Substances 0.000 claims description 9
150000001989 diazonium salts Chemical class 0.000 claims description 8
229920000642 polymer Polymers 0.000 claims description 8
229920002678 cellulose Polymers 0.000 claims description 7
239000012954 diazonium Substances 0.000 claims description 7
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 6
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
239000005977 Ethylene Substances 0.000 claims description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
229920000180 alkyd Polymers 0.000 claims description 3
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 2
239000000243 solution Substances 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 8
235000002639 sodium chloride Nutrition 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical class COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
239000000126 substance Substances 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 5
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
238000007792 addition Methods 0.000 description 4
229910021529 ammonia Inorganic materials 0.000 description 4
239000000203 mixture Substances 0.000 description 4
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
239000011592 zinc chloride Substances 0.000 description 4
235000005074 zinc chloride Nutrition 0.000 description 4
YCPXWRQRBFJBPZ-UHFFFAOYSA-N 5-sulfosalicylic acid Chemical compound OC(=O)C1=CC(S(O)(=O)=O)=CC=C1O YCPXWRQRBFJBPZ-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
230000001133 acceleration Effects 0.000 description 3
239000001913 cellulose 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
239000000975 dye Substances 0.000 description 3
UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
YKYOUMDCQGMQQO-UHFFFAOYSA-L cadmium dichloride Chemical compound Cl[Cd]Cl YKYOUMDCQGMQQO-UHFFFAOYSA-L 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
238000010791 quenching Methods 0.000 description 2
230000000171 quenching effect Effects 0.000 description 2
150000004760 silicates Chemical class 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
239000002966 varnish Substances 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
MXZROAOUCUVNHX-UHFFFAOYSA-N 2-Aminopropanol Chemical compound CCC(N)O MXZROAOUCUVNHX-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical group CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
ADOGRHNJEKVFAC-UHFFFAOYSA-N 3-methyl-4-pyrrolidin-1-ylbenzenediazonium Chemical class CC1=CC([N+]#N)=CC=C1N1CCCC1 ADOGRHNJEKVFAC-UHFFFAOYSA-N 0.000 description 1
IZHYJUURSCQKMN-UHFFFAOYSA-M 3-methyl-4-pyrrolidin-1-ylbenzenediazonium;chloride Chemical compound [Cl-].CC1=CC([N+]#N)=CC=C1N1CCCC1 IZHYJUURSCQKMN-UHFFFAOYSA-M 0.000 description 1
YSWBFLWKAIRHEI-UHFFFAOYSA-N 4,5-dimethyl-1h-imidazole Chemical compound CC=1N=CNC=1C YSWBFLWKAIRHEI-UHFFFAOYSA-N 0.000 description 1
WCDSVWRUXWCYFN-UHFFFAOYSA-N 4-aminobenzenethiol Chemical class NC1=CC=C(S)C=C1 WCDSVWRUXWCYFN-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 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
229910019142 PO4 Inorganic materials 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
229920000147 Styrene maleic anhydride Polymers 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
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
GCPWJFKTWGFEHH-UHFFFAOYSA-N acetoacetamide Chemical compound CC(=O)CC(N)=O GCPWJFKTWGFEHH-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
150000003927 aminopyridines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
238000009835 boiling Methods 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
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical class FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
239000000969 carrier Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
229910052681 coesite Inorganic materials 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229910052906 cristobalite Inorganic materials 0.000 description 1
DGJMPUGMZIKDRO-UHFFFAOYSA-N cyanoacetamide Chemical compound NC(=O)CC#N DGJMPUGMZIKDRO-UHFFFAOYSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000013773 glyceryl triacetate Nutrition 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
229920001477 hydrophilic polymer Polymers 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000005286 illumination Methods 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
230000001404 mediated effect Effects 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
238000000034 method Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
150000004989 p-phenylenediamines Chemical class 0.000 description 1
150000007965 phenolic acids Chemical class 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
229960002622 triacetin Drugs 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- 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

Landscapes

Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
General Physics & Mathematics (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Paper (AREA)
Developing Agents For Electrophotography (AREA)

NO773984A 1976-11-22 1977-11-21 Tokomponent-diazotypimaterial. NO773984L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2652942A DE2652942C3 (de)	1976-11-22	1976-11-22	Zweikomponenten-Diazotypiematerial

Publications (1)

Publication Number	Publication Date
NO773984L true NO773984L (no)	1978-05-23

Family

ID=5993659

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO773984A NO773984L (no)	1976-11-22	1977-11-21	Tokomponent-diazotypimaterial.

Country Status (19)

Country	Link
US (1)	US4171222A (de)
JP (1)	JPS5365721A (de)
AR (1)	AR218644A1 (de)
AT (1)	AT356513B (de)
AU (1)	AU515959B2 (de)
BE (1)	BE861023A (de)
BR (1)	BR7707712A (de)
CA (1)	CA1107997A (de)
CH (1)	CH630470A5 (de)
DE (1)	DE2652942C3 (de)
DK (1)	DK515377A (de)
ES (1)	ES464338A1 (de)
FI (1)	FI773518A7 (de)
FR (1)	FR2371709A1 (de)
GB (1)	GB1595347A (de)
IT (1)	IT1091789B (de)
NL (1)	NL186658C (de)
NO (1)	NO773984L (de)
SE (1)	SE417759B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3100580A1 (de) *	1981-01-10	1982-08-26	Hoechst Ag, 6000 Frankfurt	Zweikomponenten-diazotypiematerial
DE3100579A1 (de) *	1981-01-10	1982-08-26	Hoechst Ag, 6000 Frankfurt	Zweikomponenten-diazotypiematerial
DE3315977A1 (de) *	1983-05-02	1984-11-08	Hoechst Ag, 6230 Frankfurt	Haftmasse
DE3418469A1 (de) *	1984-05-18	1985-11-21	Hoechst Ag, 6230 Frankfurt	Lichtempfindliches gemisch und hiermit hergestelltes zweikomponenten-diazotypiematerial
JP2000047346A (ja) *	1998-07-31	2000-02-18	Somar Corp	ジアゾ感光材料
US6861262B2 (en) *	2000-03-03	2005-03-01	Quest Diagnostics Investments Incorporated	Composition and method for detecting an adulterant in an aqueous sample
WO2000052464A1 (en) *	1999-03-04	2000-09-08	Quest Diagnostics Investments Incorporated	Reagent and method for detecting an adulterant in an aqueous sample

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2990281A (en) *	1956-12-17	1961-06-27	Monsanto Chemicals	Photosensitive resinous compositions and photographic elements
US3316092A (en) *	1963-05-09	1967-04-25	Dietzgen Co Eugene	Diazotype material comprising a metal sulfate nitrogenous compound and polymeric anhydride
BE755280A (fr) *	1969-08-26	1971-02-01	Eastman Kodak Co	Nouveau produit photosensible pour diazotypie
DE2123702C3 (de) *	1971-05-13	1988-05-26	Hoechst Ag, 6230 Frankfurt	Verfahren zur Herstellung eines Reliefbildes

1976
- 1976-11-22 DE DE2652942A patent/DE2652942C3/de not_active Expired
1977
- 1977-11-17 CH CH1408377A patent/CH630470A5/de not_active IP Right Cessation
- 1977-11-18 CA CA291,183A patent/CA1107997A/en not_active Expired
- 1977-11-18 AU AU30766/77A patent/AU515959B2/en not_active Expired
- 1977-11-18 NL NLAANVRAGE7712727,A patent/NL186658C/xx not_active IP Right Cessation
- 1977-11-18 SE SE7713031A patent/SE417759B/sv unknown
- 1977-11-18 IT IT51852/77A patent/IT1091789B/it active
- 1977-11-21 GB GB48348/77A patent/GB1595347A/en not_active Expired
- 1977-11-21 BE BE182787A patent/BE861023A/xx unknown
- 1977-11-21 ES ES464338A patent/ES464338A1/es not_active Expired
- 1977-11-21 BR BR7707712A patent/BR7707712A/pt unknown
- 1977-11-21 DK DK515377A patent/DK515377A/da not_active Application Discontinuation
- 1977-11-21 FI FI773518A patent/FI773518A7/fi not_active Application Discontinuation
- 1977-11-21 US US05/853,519 patent/US4171222A/en not_active Expired - Lifetime
- 1977-11-21 FR FR7734854A patent/FR2371709A1/fr active Granted
- 1977-11-21 AT AT830277A patent/AT356513B/de not_active IP Right Cessation
- 1977-11-21 AR AR270044A patent/AR218644A1/es active
- 1977-11-21 NO NO773984A patent/NO773984L/no unknown
- 1977-11-22 JP JP14057277A patent/JPS5365721A/ja active Pending

Also Published As

Publication number	Publication date
DE2652942A1 (de)	1978-05-24
SE417759B (sv)	1981-04-06
NL186658C (nl)	1991-01-16
DK515377A (da)	1978-05-23
AU515959B2 (en)	1981-05-14
DE2652942B2 (de)	1978-10-05
NL186658B (nl)	1990-08-16
NL7712727A (nl)	1978-05-24
US4171222A (en)	1979-10-16
IT1091789B (it)	1985-07-06
FR2371709A1 (fr)	1978-06-16
CA1107997A (en)	1981-09-01
DE2652942C3 (de)	1979-05-31
GB1595347A (en)	1981-08-12
AR218644A1 (es)	1980-06-30
CH630470A5 (de)	1982-06-15
FR2371709B1 (de)	1981-09-11
JPS5365721A (en)	1978-06-12
BR7707712A (pt)	1978-07-25
AU3076677A (en)	1979-05-24
BE861023A (fr)	1978-05-22
ATA830277A (de)	1979-09-15
SE7713031L (sv)	1978-05-23
AT356513B (de)	1980-05-12
ES464338A1 (es)	1978-12-01
FI773518A7 (fi)	1978-05-23

Publication	Publication Date	Title
US2980534A (en)	1961-04-18	Photographic compositions and photographic elements
US3446651A (en)	1969-05-27	Plastic film coated with antistatic agent
EP0030352B1 (de)	1984-08-15	Nicht substrierter organischer Film, der mit einer opaken antistatischen Rückschicht beschichtet ist, und Verfahren zur Herstellung
US3262807A (en)	1966-07-26	Articles resistant to static buildup
US4879064A (en)	1989-11-07	Electroconductive coating composition
NO773984L (no)	1978-05-23	Tokomponent-diazotypimaterial.
US3666532A (en)	1972-05-30	Dimensionally stable matte-surfaced polyester drafting film
JPH07115450B2 (ja)	1995-12-13	製図材料
JPH0368823B2 (de)	1991-10-29
US4471043A (en)	1984-09-11	Diazotype material
US4039333A (en)	1977-08-02	Photographic materials having improved anti-halation layers
US3573951A (en)	1971-04-06	Preparation of synthetic film materials
US4219616A (en)	1980-08-26	Recording materials for vesicular imaging
US5156707A (en)	1992-10-20	Support for photographic printing paper
US3057722A (en)	1962-10-09	Photographic stripping film
US5223372A (en)	1993-06-29	Chemical mat film and a photosensitive film comprising an o-naphthoquinine diazide compound and a binder coated over the chemical mat film
US3834928A (en)	1974-09-10	Process for producing photographic material
US3091532A (en)	1963-05-28	Vesicular image photography process with polyketone photographic films
US3925080A (en)	1975-12-09	Multi-layered photosensitive material having glass substrate and method of manufacture
US3622335A (en)	1971-11-23	Copolymers of an alpha acrylonitrile and a styrene used as vehicles in vesicular materials
US3518040A (en)	1970-06-30	Formation of urethane units on the surface of polycarbonate structures
US3392022A (en)	1968-07-09	Removable antihalation layers for photographic film
GB1600886A (en)	1981-10-21	Vesicular material
US2755186A (en)	1956-07-17	Photographic films
NO820044L (no)	1982-07-12	Tokomponent-diazotypiematerial