NO772358L - Fremgangsm}te til fremstilling av bindemidler for elektrodyppelakkering - Google Patents
Fremgangsm}te til fremstilling av bindemidler for elektrodyppelakkeringInfo
- Publication number
- NO772358L NO772358L NO772358A NO772358A NO772358L NO 772358 L NO772358 L NO 772358L NO 772358 A NO772358 A NO 772358A NO 772358 A NO772358 A NO 772358A NO 772358 L NO772358 L NO 772358L
- Authority
- NO
- Norway
- Prior art keywords
- unsaturated
- mol
- reaction
- acid
- isocyanate
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 26
- 238000002360 preparation method Methods 0.000 title description 2
- 238000006243 chemical reaction Methods 0.000 claims description 45
- 239000002253 acid Substances 0.000 claims description 23
- 239000011230 binding agent Substances 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 239000007795 chemical reaction product Substances 0.000 claims description 22
- 239000012948 isocyanate Substances 0.000 claims description 21
- 239000002243 precursor Substances 0.000 claims description 20
- -1 hydroxyalkyl acrylates Chemical class 0.000 claims description 18
- 239000000047 product Substances 0.000 claims description 18
- 125000001931 aliphatic group Chemical group 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 17
- 150000002513 isocyanates Chemical class 0.000 claims description 15
- 229920006395 saturated elastomer Polymers 0.000 claims description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 150000007513 acids Chemical class 0.000 claims description 10
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 10
- 239000005056 polyisocyanate Substances 0.000 claims description 10
- 229920001228 polyisocyanate Polymers 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 9
- 125000005442 diisocyanate group Chemical group 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 238000006386 neutralization reaction Methods 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000003700 epoxy group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000003618 dip coating Methods 0.000 claims description 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 4
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims description 4
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 3
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 3
- 150000008064 anhydrides Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- 238000006068 polycondensation reaction Methods 0.000 claims description 2
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 2
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 2
- 239000012084 conversion product Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 230000007306 turnover Effects 0.000 claims 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 13
- 238000001723 curing Methods 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 10
- 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 10
- 239000011248 coating agent Substances 0.000 description 10
- 239000003822 epoxy resin Substances 0.000 description 9
- 229920000647 polyepoxide Polymers 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
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- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 230000007717 exclusion Effects 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 229920002521 macromolecule Polymers 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
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- 238000012719 thermal polymerization Methods 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
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- 238000004132 cross linking Methods 0.000 description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002118 epoxides Chemical group 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical class OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 229920003180 amino resin Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
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- 150000002989 phenols Chemical class 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
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- 239000001294 propane Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
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- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
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- IKYKEVDKGZYRMQ-PDBXOOCHSA-N (9Z,12Z,15Z)-octadecatrien-1-ol Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCCO IKYKEVDKGZYRMQ-PDBXOOCHSA-N 0.000 description 1
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- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
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- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
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- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- ALSTYHKOOCGGFT-MDZDMXLPSA-N oleyl alcohol Chemical compound CCCCCCCC\C=C\CCCCCCCCO ALSTYHKOOCGGFT-MDZDMXLPSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D13/00—Electrophoretic coating characterised by the process
- C25D13/04—Electrophoretic coating characterised by the process with organic material
- C25D13/06—Electrophoretic coating characterised by the process with organic material with polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/6705—Unsaturated polymers not provided for in the groups C08G18/671, C08G18/6795, C08G18/68 or C08G18/69
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
- C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
- C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
- C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4419—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications with polymers obtained otherwise than by polymerisation reactions only involving carbon-to-carbon unsaturated bonds
- C09D5/4465—Polyurethanes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/901—Electrodepositable compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Molecular Biology (AREA)
- Electrochemistry (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Polyurethanes Or Polyureas (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Paints Or Removers (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Ink Jet (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT528476A AT342169B (de) | 1976-07-19 | 1976-07-19 | Verfahren zur herstellung von bindemitteln fur die elektrotauchlackierung |
AT806976A AT353907B (de) | 1976-07-19 | 1976-10-29 | Verfahren zur herstellung von bindemitteln fuer die elektrotauchlackierung |
AT806876A AT348635B (de) | 1976-07-19 | 1976-10-29 | Verfahren zur herstellung von bindemitteln fuer die elektrotauchlackierung |
AT945576A AT358684B (de) | 1976-12-20 | 1976-12-20 | Verfahren zur herstellung von bindemitteln fuer die elektrotauchlackierung |
Publications (1)
Publication Number | Publication Date |
---|---|
NO772358L true NO772358L (no) | 1978-01-20 |
Family
ID=27422104
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO772358A NO772358L (no) | 1976-07-19 | 1977-07-04 | Fremgangsm}te til fremstilling av bindemidler for elektrodyppelakkering |
Country Status (25)
Country | Link |
---|---|
US (1) | US4238594A (pt) |
JP (1) | JPS5312977A (pt) |
AR (1) | AR226521A1 (pt) |
AU (1) | AU509220B2 (pt) |
BE (1) | BE856826A (pt) |
BR (1) | BR7704732A (pt) |
CA (1) | CA1124938A (pt) |
CH (1) | CH634342A5 (pt) |
CS (1) | CS223863B2 (pt) |
DD (1) | DD133812A5 (pt) |
DE (1) | DE2707405C3 (pt) |
DK (1) | DK320977A (pt) |
ES (1) | ES460629A1 (pt) |
FR (1) | FR2359190A1 (pt) |
GB (1) | GB1551496A (pt) |
GR (1) | GR63569B (pt) |
HU (1) | HU178369B (pt) |
IT (1) | IT1081284B (pt) |
MX (1) | MX148264A (pt) |
NL (1) | NL7707637A (pt) |
NO (1) | NO772358L (pt) |
PL (1) | PL103110B1 (pt) |
RO (1) | RO72770A (pt) |
SE (1) | SE433944B (pt) |
YU (1) | YU172477A (pt) |
Families Citing this family (71)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT343770B (de) * | 1976-12-13 | 1978-06-12 | Vianova Kunstharz Ag | Verfahren zur herstellung von warmehartbaren bindemitteln fur kathodisch abscheidbare uberzugsmittel |
AT356226B (de) * | 1977-10-24 | 1980-04-10 | Vianova Kunstharz Ag | Verfahren zur herstellung kathodisch ab- scheidbarer bindemittel |
US4395502A (en) * | 1977-12-01 | 1983-07-26 | Vianova Kunstharz, A.G. | Cathodically depositable coating compositions for electrodeposition (II) |
US4403050A (en) * | 1977-12-19 | 1983-09-06 | Vianova Kunstharz, A. G. | Cathodically depositable ester-containing coating compositions |
AT357247B (de) * | 1978-12-27 | 1980-06-25 | Vianova Kunstharz Ag | Verfahren zur herstellung von selbstver- netzenden bindemitteln fuer kathodisch abscheid- bare elektrotauchlacke |
AT362479B (de) * | 1979-06-22 | 1981-05-25 | Vianova Kunstharz Ag | Verfahren zur herstellung von bindemitteln fuer die elektrotauchlackierung |
DE2928769A1 (de) * | 1979-07-17 | 1981-02-12 | Nippon Paint Co Ltd | Harz und dieses enthaltender elektrophoretischer anstrichstoff |
AT366401B (de) * | 1979-11-05 | 1982-04-13 | Vianova Kunstharz Ag | Verfahren zur herstellung von wasserverduennbaren, oxazolidingruppen tragenden bindemitteln |
US4514549A (en) * | 1983-01-05 | 1985-04-30 | Ford Motor Company | Crosslinkable composition of matter-IV |
US4514548A (en) * | 1983-01-05 | 1985-04-30 | Ford Motor Company | Crosslinkable composition of matter-I |
AT375953B (de) * | 1983-03-21 | 1984-09-25 | Vianova Kunstharz Ag | Verfahren zur herstellung von selbstvernetzenden, kathodisch abscheidbaren etl-bindemitteln auf basis modifizierter alkylphenol-formaldehyd -kondensationsprodukte |
US4559393A (en) * | 1983-12-27 | 1985-12-17 | Ford Motor Company | Crosslinkable composition comprising aminoepoxy resin - III |
US4582880A (en) * | 1983-12-27 | 1986-04-15 | Ford Motor Company | Crosslinkable composition comprising aminoepoxy resins-1 |
US4565852A (en) * | 1983-12-27 | 1986-01-21 | Ford Motor Company | Crosslinkable composition comprising aminoepoxy resin-II |
AT379414B (de) * | 1984-01-27 | 1986-01-10 | Vianova Kunstharz Ag | Verfahren zur herstellung von mehrschichtlackierungen |
US4720523A (en) * | 1984-12-10 | 1988-01-19 | E. I. Du Pont De Nemours And Company | Blocked dieneophile functional modified aminoepoxy resins |
US4619977A (en) * | 1984-12-10 | 1986-10-28 | Ford Motor Company | Crosslinkable composition comprising aminoepoxy resin-IV |
US4639493A (en) * | 1984-12-10 | 1987-01-27 | Ford Motor Company | Conjugated diene functional modified aminoepoxy resins |
US4617348A (en) * | 1984-12-10 | 1986-10-14 | Ford Motor Company | Crosslinkable composition comprising modified aminoepoxy resins-II |
DE3530179A1 (de) * | 1985-08-23 | 1987-02-26 | Herberts Gmbh | Kathodisch abscheidbares waessriges elektrotauchlack-ueberzugsmittel |
JPH0786125B2 (ja) * | 1985-10-09 | 1995-09-20 | 日本ペイント株式会社 | 反応性微小樹脂粒子、その製法ならびに硬化組成物 |
DE3615810A1 (de) * | 1986-05-10 | 1987-11-12 | Herberts Gmbh | Kathodisch abscheidbares waessriges elektrotauchlackueberzugsmittel und seine verwendung |
AU626269B2 (en) * | 1987-09-18 | 1992-07-30 | Rheox International, Inc. | Water dispersible, modified polyurethane thickener with improved high shear viscosity in aqueous systems |
US5023309A (en) * | 1987-09-18 | 1991-06-11 | Rheox, Inc. | Water dispersible, modified polyurethane thickener with improved high shear viscosity in aqueous systems |
DE4025687A1 (de) * | 1990-08-14 | 1992-02-20 | Ruetgerswerke Ag | Durch strahlung vernetzbare bindemittelgemische |
US5223373A (en) * | 1991-04-29 | 1993-06-29 | Industrial Technology Research Institute | Positive working photosensitive composition and photosensitive electrodeposition composition prepared therefrom |
ES2098602T5 (es) † | 1992-08-07 | 2000-12-01 | Bayer Ag | Resinas multifuncionales exentas de cloro para el acabado del papel. |
DE4331061A1 (de) * | 1993-09-13 | 1995-03-16 | Hoechst Ag | Lösemittelfreie, wäßrige Kunstharzdispersion |
DE4413059A1 (de) * | 1994-04-15 | 1996-01-25 | Hoechst Ag | Wäßrige Beschichtungsmittel enthaltend lösungsmittelfrei dispergierbare Härter |
TW282479B (pt) * | 1994-06-30 | 1996-08-01 | Hoechst Ag | |
DE4423139A1 (de) | 1994-07-01 | 1996-01-04 | Hoechst Ag | Härtung von kataphoretischen Tauchlacken mit Wismutkatalysatoren |
US7046126B2 (en) | 1996-08-22 | 2006-05-16 | Omega Patents, L.L.C. | Vehicle window control system for a vehicle having a data communications bus and associated methods |
US5908912A (en) * | 1996-09-06 | 1999-06-01 | Ppg Industries Ohio, Inc. | Electrodepositable coating composition containing bismuth and amino acid materials and electrodeposition method |
US6017431A (en) * | 1997-07-17 | 2000-01-25 | Ppg Industries Ohio, Inc. | Cationic electrodepositable coating composition and bath thereof and process for retarding the growth of bacteria for such a bath |
US6025068A (en) * | 1998-02-13 | 2000-02-15 | Ppg Industries Ohio, Inc. | Inkjet printable coating for microporous materials |
US6423425B1 (en) | 1998-05-26 | 2002-07-23 | Ppg Industries Ohio, Inc. | Article having a chip-resistant electrodeposited coating and a process for forming an electrodeposited coating |
US6248225B1 (en) | 1998-05-26 | 2001-06-19 | Ppg Industries Ohio, Inc. | Process for forming a two-coat electrodeposited composite coating the composite coating and chip resistant electrodeposited coating composition |
EP1311638A4 (en) * | 2000-08-10 | 2005-01-19 | Akzo Nobel Coatings Int Bv | COATING COMPOSITIONS |
US6676820B2 (en) | 2001-03-02 | 2004-01-13 | Ppg Industries Ohio, Inc. | Process for electrocoating metal blanks and coiled metal substrates |
US6951707B2 (en) | 2001-03-08 | 2005-10-04 | Ppg Industries Ohio, Inc. | Process for creating vias for circuit assemblies |
US6713587B2 (en) | 2001-03-08 | 2004-03-30 | Ppg Industries Ohio, Inc. | Electrodepositable dielectric coating compositions and methods related thereto |
US7000313B2 (en) | 2001-03-08 | 2006-02-21 | Ppg Industries Ohio, Inc. | Process for fabricating circuit assemblies using electrodepositable dielectric coating compositions |
US6824959B2 (en) | 2002-06-27 | 2004-11-30 | Ppg Industries Ohio, Inc. | Process for creating holes in polymeric substrates |
US20060213685A1 (en) * | 2002-06-27 | 2006-09-28 | Wang Alan E | Single or multi-layer printed circuit board with improved edge via design |
JP2005531160A (ja) * | 2002-06-27 | 2005-10-13 | ピーピージー インダストリーズ オハイオ, インコーポレイテッド | 窪んだかまたは広がったブレイクアウェイタブを有する単層または多層のプリント回路基板およびその製造方法 |
CA2530122C (en) | 2003-06-24 | 2010-09-28 | Ppg Industries Ohio, Inc. | Aqueous dispersions of microparticles having a nanoparticulate phase and coating compositions containing the same |
US20050208319A1 (en) * | 2004-03-22 | 2005-09-22 | Finley James J | Methods for forming an electrodeposited coating over a coated substrate and articles made thereby |
EP1829944A1 (en) * | 2006-03-01 | 2007-09-05 | Cytec Surface Specialties Austria GmbH | Water-borne cationic binders for wash primers |
US8282801B2 (en) | 2008-12-18 | 2012-10-09 | Ppg Industries Ohio, Inc. | Methods for passivating a metal substrate and related coated metal substrates |
US10017861B2 (en) | 2011-08-03 | 2018-07-10 | Ppg Industries Ohio, Inc. | Zirconium pretreatment compositions containing a rare earth metal, associated methods for treating metal substrates, and related coated metal substrates |
US20130230425A1 (en) | 2011-09-02 | 2013-09-05 | Ppg Industries Ohio, Inc. | Two-step zinc phosphating process |
US20130081950A1 (en) | 2011-09-30 | 2013-04-04 | Ppg Industries Ohio, Inc. | Acid cleaners for metal substrates and associated methods for cleaning and coating metal substrates |
US8852357B2 (en) | 2011-09-30 | 2014-10-07 | Ppg Industries Ohio, Inc | Rheology modified pretreatment compositions and associated methods of use |
US20130146460A1 (en) | 2011-12-13 | 2013-06-13 | Ppg Industries Ohio, Inc. | Resin based post rinse for improved throwpower of electrodepositable coating compositions on pretreated metal substrates |
MY169256A (en) | 2012-08-29 | 2019-03-19 | Ppg Ind Ohio Inc | Zirconium pretreatment compositions containing lithium, associated methods for treating metal substrates, and related coated metal substrates |
IN2015DN01537A (pt) | 2012-08-29 | 2015-07-03 | Ppg Ind Ohio Inc | |
CN105026615A (zh) | 2013-03-06 | 2015-11-04 | Ppg工业俄亥俄公司 | 处理铁类金属基底的方法 |
US20140255608A1 (en) | 2013-03-11 | 2014-09-11 | Ppg Industries Ohio, Inc. | Coatings that exhibit a tri-coat appearance, related coating methods and substrates |
US9273399B2 (en) | 2013-03-15 | 2016-03-01 | Ppg Industries Ohio, Inc. | Pretreatment compositions and methods for coating a battery electrode |
US9068089B2 (en) | 2013-03-15 | 2015-06-30 | Ppg Industries Ohio, Inc. | Phenolic admix for electrodepositable coating composition containing a cyclic guanidine |
US9303167B2 (en) | 2013-03-15 | 2016-04-05 | Ppg Industries Ohio, Inc. | Method for preparing and treating a steel substrate |
US20150315718A1 (en) | 2014-05-05 | 2015-11-05 | Ppg Industries Ohio, Inc. | Metal pretreatment modification for improved throwpower |
US10173176B2 (en) | 2015-04-29 | 2019-01-08 | Ppg Industries Ohio, Inc. | Method for preparing a resin-treated microporous membrane |
US10113070B2 (en) | 2015-11-04 | 2018-10-30 | Ppg Industries Ohio, Inc. | Pretreatment compositions and methods of treating a substrate |
US20170306497A1 (en) | 2016-04-25 | 2017-10-26 | Ppg Industries Ohio, Inc. | System for nickel-free zinc phosphate pretreatment |
US20170306498A1 (en) | 2016-04-25 | 2017-10-26 | Ppg Industries Ohio, Inc. | Activating rinse and method for treating a substrate |
US10329437B2 (en) | 2016-06-30 | 2019-06-25 | Ppg Industries Ohio, Inc. | Electrodepositable coating composition having improved crater control |
KR102266260B1 (ko) | 2016-06-30 | 2021-06-16 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 개선된 크레이터 제어능을 갖는 전착성 코팅 조성물 |
WO2018039462A1 (en) | 2016-08-24 | 2018-03-01 | Ppg Industries Ohio, Inc. | Alkaline composition for treating metal substartes |
US10370545B2 (en) | 2017-09-19 | 2019-08-06 | Ppg Industries Ohio, Inc. | Low VOC anionic electrodepositable coating composition |
CN116854975B (zh) * | 2023-07-11 | 2024-04-05 | 合肥乐凯科技产业有限公司 | 一种防静电膜及制备方法 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3799854A (en) * | 1970-06-19 | 1974-03-26 | Ppg Industries Inc | Method of electrodepositing cationic compositions |
FR2100794B1 (pt) | 1970-06-19 | 1973-12-28 | Ppg Industries Inc | |
US3804786A (en) * | 1971-07-14 | 1974-04-16 | Desoto Inc | Water-dispersible cationic polyurethane resins |
FR2150658B1 (pt) * | 1971-09-01 | 1980-08-14 | Monsanto Co | |
CA986639A (en) * | 1971-10-28 | 1976-03-30 | Robert R. Zwack | Cationic electrodepositable compositions |
JPS4923807A (pt) * | 1972-06-28 | 1974-03-02 | ||
JPS5110879B2 (pt) * | 1972-08-25 | 1976-04-07 | ||
CA1024291A (en) | 1972-12-22 | 1978-01-10 | Ppg Industries, Inc. | Self-crosslinking cationic electrodepositable compositions |
JPS5139900B2 (pt) * | 1973-10-20 | 1976-10-30 | ||
CH574080A5 (pt) | 1974-07-25 | 1976-03-31 | Bbc Brown Boveri & Cie | |
US4036800A (en) * | 1975-06-04 | 1977-07-19 | Desoto, Inc. | Electrodeposition of aqueous dispersions of amine functional urethane copolymers |
US4096105A (en) * | 1976-05-24 | 1978-06-20 | Scm Corporation | Aqueous coating composition |
US4147679A (en) * | 1976-06-02 | 1979-04-03 | Ppg Industries, Inc. | Water-reduced urethane coating compositions |
US4069210A (en) * | 1976-09-30 | 1978-01-17 | Ppg Industries, Inc. | Polymeric products |
-
1977
- 1977-02-21 DE DE2707405A patent/DE2707405C3/de not_active Expired
- 1977-06-13 SE SE7706831A patent/SE433944B/xx not_active IP Right Cessation
- 1977-06-16 CH CH743177A patent/CH634342A5/de not_active IP Right Cessation
- 1977-07-04 NO NO772358A patent/NO772358L/no unknown
- 1977-07-08 NL NL7707637A patent/NL7707637A/xx not_active Application Discontinuation
- 1977-07-11 ES ES460629A patent/ES460629A1/es not_active Expired
- 1977-07-11 YU YU01724/77A patent/YU172477A/xx unknown
- 1977-07-11 FR FR7721293A patent/FR2359190A1/fr active Granted
- 1977-07-11 IT IT25591/77A patent/IT1081284B/it active
- 1977-07-14 BE BE179355A patent/BE856826A/xx unknown
- 1977-07-14 DK DK320977A patent/DK320977A/da not_active Application Discontinuation
- 1977-07-15 DD DD7700200099A patent/DD133812A5/xx unknown
- 1977-07-18 CA CA282,990A patent/CA1124938A/en not_active Expired
- 1977-07-18 RO RO7791080A patent/RO72770A/ro unknown
- 1977-07-18 BR BR7704732A patent/BR7704732A/pt unknown
- 1977-07-18 GB GB30108/77A patent/GB1551496A/en not_active Expired
- 1977-07-18 HU HU77VI1140A patent/HU178369B/hu unknown
- 1977-07-18 PL PL1977199721A patent/PL103110B1/pl unknown
- 1977-07-18 GR GR53978A patent/GR63569B/el unknown
- 1977-07-19 US US05/816,936 patent/US4238594A/en not_active Expired - Lifetime
- 1977-07-19 CS CS774813A patent/CS223863B2/cs unknown
- 1977-07-19 AR AR268478A patent/AR226521A1/es active
- 1977-07-19 AU AU27124/77A patent/AU509220B2/en not_active Expired
- 1977-07-19 JP JP8658677A patent/JPS5312977A/ja active Granted
- 1977-07-19 MX MX169913A patent/MX148264A/es unknown
Also Published As
Publication number | Publication date |
---|---|
PL103110B1 (pl) | 1979-05-31 |
CS223863B2 (en) | 1983-11-25 |
FR2359190A1 (fr) | 1978-02-17 |
CA1124938A (en) | 1982-06-01 |
AU2712477A (en) | 1979-01-25 |
IT1081284B (it) | 1985-05-16 |
DK320977A (da) | 1978-01-20 |
AU509220B2 (en) | 1980-05-01 |
PL199721A1 (pl) | 1978-03-13 |
DE2707405A1 (de) | 1978-01-26 |
JPS5312977A (en) | 1978-02-06 |
CH634342A5 (de) | 1983-01-31 |
DD133812A5 (de) | 1979-01-24 |
DE2707405C3 (de) | 1987-12-03 |
YU172477A (en) | 1982-06-30 |
MX148264A (es) | 1983-04-05 |
ES460629A1 (es) | 1978-05-16 |
AR226521A1 (es) | 1982-07-30 |
SE433944B (sv) | 1984-06-25 |
GR63569B (en) | 1979-11-20 |
US4238594A (en) | 1980-12-09 |
NL7707637A (nl) | 1978-01-23 |
RO72770B (ro) | 1983-08-30 |
HU178369B (en) | 1982-04-28 |
SE7706831L (sv) | 1978-01-20 |
GB1551496A (en) | 1979-08-30 |
FR2359190B1 (pt) | 1979-03-09 |
BR7704732A (pt) | 1978-04-04 |
DE2707405B2 (de) | 1982-09-16 |
RO72770A (ro) | 1983-09-26 |
JPS5415786B2 (pt) | 1979-06-18 |
BE856826A (fr) | 1977-10-31 |
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