DE19736920A1 - Wäßriges Beschichtungsmittel für Einbrennlackierung und Verfahren zu seiner Herstellung - Google Patents
Wäßriges Beschichtungsmittel für Einbrennlackierung und Verfahren zu seiner HerstellungInfo
- Publication number
- DE19736920A1 DE19736920A1 DE19736920A DE19736920A DE19736920A1 DE 19736920 A1 DE19736920 A1 DE 19736920A1 DE 19736920 A DE19736920 A DE 19736920A DE 19736920 A DE19736920 A DE 19736920A DE 19736920 A1 DE19736920 A1 DE 19736920A1
- Authority
- DE
- Germany
- Prior art keywords
- weight
- group content
- cyclo
- polyester
- parts
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims description 23
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- 239000006185 dispersion Substances 0.000 claims abstract description 42
- 229920005862 polyol Polymers 0.000 claims abstract description 41
- 150000003077 polyols Chemical class 0.000 claims abstract description 40
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 31
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 31
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 30
- 229920000728 polyester Polymers 0.000 claims abstract description 27
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 26
- 238000000576 coating method Methods 0.000 claims abstract description 23
- 239000002904 solvent Substances 0.000 claims abstract description 23
- 239000011248 coating agent Substances 0.000 claims abstract description 20
- 239000000654 additive Substances 0.000 claims abstract description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 12
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 12
- 230000003472 neutralizing effect Effects 0.000 claims abstract description 11
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 7
- 238000001035 drying Methods 0.000 claims abstract description 6
- 239000002562 thickening agent Substances 0.000 claims abstract description 6
- 239000006096 absorbing agent Substances 0.000 claims abstract description 5
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 5
- 239000003139 biocide Substances 0.000 claims abstract description 5
- 239000003054 catalyst Substances 0.000 claims abstract description 5
- 238000007872 degassing Methods 0.000 claims abstract description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 21
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 19
- 239000000178 monomer Substances 0.000 claims description 19
- 230000009477 glass transition Effects 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 15
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- 239000000126 substance Substances 0.000 claims description 13
- 229920005906 polyester polyol Polymers 0.000 claims description 12
- 125000005907 alkyl ester group Chemical group 0.000 claims description 11
- 239000011230 binding agent Substances 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000000047 product Substances 0.000 claims description 10
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 9
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 9
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- 239000012071 phase Substances 0.000 claims description 8
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- 150000001875 compounds Chemical class 0.000 claims description 7
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- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 5
- 238000011065 in-situ storage Methods 0.000 claims description 5
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 4
- 239000007764 o/w emulsion Substances 0.000 claims description 4
- 239000002516 radical scavenger Substances 0.000 claims description 4
- PJMDLNIAGSYXLA-UHFFFAOYSA-N 6-iminooxadiazine-4,5-dione Chemical group N=C1ON=NC(=O)C1=O PJMDLNIAGSYXLA-UHFFFAOYSA-N 0.000 claims description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 239000007762 w/o emulsion Substances 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 2
- 239000012074 organic phase Substances 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 2
- 229940070721 polyacrylate Drugs 0.000 claims 4
- 239000010410 layer Substances 0.000 claims 2
- 210000003298 dental enamel Anatomy 0.000 claims 1
- 239000002356 single layer Substances 0.000 claims 1
- 239000000843 powder Substances 0.000 abstract description 17
- 239000004971 Cross linker Substances 0.000 abstract description 7
- 239000012948 isocyanate Substances 0.000 abstract description 5
- 150000002513 isocyanates Chemical class 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 36
- -1 alkyl radical Chemical class 0.000 description 26
- 239000003973 paint Substances 0.000 description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 15
- 239000000203 mixture Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 11
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 239000010408 film Substances 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 7
- 239000005058 Isophorone diisocyanate Substances 0.000 description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- 239000002981 blocking agent Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- SDXAWLJRERMRKF-UHFFFAOYSA-N 3,5-dimethyl-1h-pyrazole Chemical compound CC=1C=C(C)NN=1 SDXAWLJRERMRKF-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000001530 fumaric acid Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 2
- 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 2
- WHIVNJATOVLWBW-PLNGDYQASA-N (nz)-n-butan-2-ylidenehydroxylamine Chemical compound CC\C(C)=N/O WHIVNJATOVLWBW-PLNGDYQASA-N 0.000 description 2
- 229940043375 1,5-pentanediol Drugs 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 2
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 2
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- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
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- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
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- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
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- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/007—After-treatment
-
- 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
- C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
- C08G18/022—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing isocyanurate 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
- C08G18/08—Processes
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/631—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyesters and/or polycarbonates
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/638—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the use of compounds having carbon-to-carbon double bonds other than styrene and/or olefinic nitriles
-
- 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
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- 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
-
- 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
- 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
- C09D5/03—Powdery paints
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Manufacturing & Machinery (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Chemically Coating (AREA)
- Ceramic Products (AREA)
- Powder Metallurgy (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19736920A DE19736920A1 (de) | 1997-08-25 | 1997-08-25 | Wäßriges Beschichtungsmittel für Einbrennlackierung und Verfahren zu seiner Herstellung |
| ES98115241T ES2176872T3 (es) | 1997-08-25 | 1998-08-13 | Procedimiento para la fabricacion de agentes de revestimiento acuosos para el lacado de secado al horno. |
| EP98115241A EP0899282B1 (de) | 1997-08-25 | 1998-08-13 | Verfahren zur Herstellung eines wässrigen Beschichtungsmittels für Einbrennlackierungen. |
| AT98115241T ATE217327T1 (de) | 1997-08-25 | 1998-08-13 | Verfahren zur herstellung eines wässrigen beschichtungsmittels für einbrennlackierungen. |
| PT98115241T PT899282E (pt) | 1997-08-25 | 1998-08-13 | Revestimento aquoso para envernizamento por cura e processo para a sua preparacao |
| DE59804030T DE59804030D1 (de) | 1997-08-25 | 1998-08-13 | Verfahren zur Herstellung eines wässrigen Beschichtungsmittels für Einbrennlackierungen. |
| US09/136,146 US6251985B1 (en) | 1997-08-25 | 1998-08-18 | Aqueous coating composition for stoving finishes and process for the production thereof |
| CA002245447A CA2245447C (en) | 1997-08-25 | 1998-08-21 | Aqueous coating composition for stoving finishes and process for the production thereof |
| BR9803763-3A BR9803763A (pt) | 1997-08-25 | 1998-08-24 | Composição aquosa de revestimento para cozimento de acabamentos e processo para sua produção. |
| KR1019980034270A KR100571467B1 (ko) | 1997-08-25 | 1998-08-24 | 스토빙피니쉬용수성코팅조성물및그의제조방법 |
| JP10251773A JPH11131017A (ja) | 1997-08-25 | 1998-08-24 | 焼付け仕上用の水性被覆組成物およびその製造方法 |
| CZ0270798A CZ296201B6 (cs) | 1997-08-25 | 1998-08-25 | Zpusob výroby vodného potahovacího prostredku provypalované nátery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19736920A DE19736920A1 (de) | 1997-08-25 | 1997-08-25 | Wäßriges Beschichtungsmittel für Einbrennlackierung und Verfahren zu seiner Herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE19736920A1 true DE19736920A1 (de) | 1999-03-04 |
Family
ID=7840073
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19736920A Withdrawn DE19736920A1 (de) | 1997-08-25 | 1997-08-25 | Wäßriges Beschichtungsmittel für Einbrennlackierung und Verfahren zu seiner Herstellung |
| DE59804030T Expired - Lifetime DE59804030D1 (de) | 1997-08-25 | 1998-08-13 | Verfahren zur Herstellung eines wässrigen Beschichtungsmittels für Einbrennlackierungen. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE59804030T Expired - Lifetime DE59804030D1 (de) | 1997-08-25 | 1998-08-13 | Verfahren zur Herstellung eines wässrigen Beschichtungsmittels für Einbrennlackierungen. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6251985B1 (enExample) |
| EP (1) | EP0899282B1 (enExample) |
| JP (1) | JPH11131017A (enExample) |
| KR (1) | KR100571467B1 (enExample) |
| AT (1) | ATE217327T1 (enExample) |
| BR (1) | BR9803763A (enExample) |
| CA (1) | CA2245447C (enExample) |
| CZ (1) | CZ296201B6 (enExample) |
| DE (2) | DE19736920A1 (enExample) |
| ES (1) | ES2176872T3 (enExample) |
| PT (1) | PT899282E (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19914885A1 (de) * | 1999-04-01 | 2000-10-05 | Bayer Ag | Dimethylpyrazol blockierte Polyurethan-Dispersionen und Polyisocyanate für Glasfaserschlichten |
| US6462139B1 (en) * | 1999-11-10 | 2002-10-08 | Ppg Industries Ohio, Inc. | Solvent-free film-forming compositions for clear coats |
| WO2001062814A2 (de) * | 2000-02-28 | 2001-08-30 | Bayer Aktiengesellschaft | Wässrige überzugsmittel für festkörperreiche einbrennlackierungen |
| US6441078B1 (en) | 2000-03-08 | 2002-08-27 | E. I. Du Pont De Nemours And Company | Aqueous powder coat dispersions, process for their preparation and their use |
| DE10129854A1 (de) * | 2001-06-21 | 2003-01-02 | Bayer Ag | Wässrige Sekundärdispersionen |
| DE10135997A1 (de) * | 2001-07-24 | 2003-02-20 | Basf Coatings Ag | Strukturviskose Klarlack-Slurry, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE10135998A1 (de) * | 2001-07-24 | 2003-02-20 | Basf Coatings Ag | Strukturviskose Klarlack-Slurry, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE10135999A1 (de) * | 2001-07-24 | 2003-02-20 | Basf Ag | Strukturviskose Klarlack-Slurry, Verfahren zu ihrer Herstellung und ihre Verwendung |
| CN1295281C (zh) * | 2002-04-23 | 2007-01-17 | 株式会社日本触媒 | 乳液聚合物树脂组合物 |
| US6884845B2 (en) * | 2002-05-20 | 2005-04-26 | Ppg Industries Ohio, Inc. | Low temperature curable, two-component, waterborne film-forming composition |
| US6881786B2 (en) * | 2002-05-20 | 2005-04-19 | Ppg Industries Ohio, Inc. | One-component, waterborne film-forming composition |
| US20050165159A1 (en) * | 2003-12-19 | 2005-07-28 | Nippon Shokubai Co., Ltd. | Acrylic resin composition dispersed in water |
| DE102004003894A1 (de) * | 2004-01-27 | 2005-08-11 | Bayer Materialscience Ag | Lösemittelarme, OH-funktionelle Dispersionen II |
| KR100644659B1 (ko) * | 2004-12-07 | 2006-11-10 | 삼성전자주식회사 | 녹업플레이트의 선단부에 용지가이드부가 마련된용지급지장치 |
| DE102006006100A1 (de) * | 2006-02-10 | 2007-08-16 | Basf Coatings Ag | Wässrige Mehrkomponentensysteme, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE102006025313A1 (de) * | 2006-05-31 | 2007-12-06 | Bayer Materialscience Ag | Lösemittelarme oder lösemittelfreie Vernetzer-Dispersion mit Pyrazol-blockierten Isocyanatgruppen |
| JP5650477B2 (ja) * | 2010-07-23 | 2015-01-07 | 太陽ホールディングス株式会社 | 導電性樹脂組成物 |
| US9796876B2 (en) * | 2012-06-20 | 2017-10-24 | Evonik Degussa Gmbh | Coating material with high scratch resistance |
| BR112015002447A2 (pt) | 2012-08-10 | 2017-07-04 | Akzo Nobel Coatings Int Bv | composição de revestimento, substrato revestido com uma composição de revestimento, e, método de revestimento de um substrato |
| CN107438635B (zh) | 2015-04-21 | 2021-01-19 | 科思创德国股份有限公司 | 制造聚异氰脲酸酯塑料的方法 |
| TW201704220A (zh) | 2015-04-21 | 2017-02-01 | 科思創德意志股份有限公司 | 聚異氰尿酸酯聚合物及製造聚異氰尿酸酯聚合物之方法 |
| US10752724B2 (en) | 2015-04-21 | 2020-08-25 | Covestro Deutschland Ag | Process for producing polyisocvanurate plastics having functionalized surfaces |
| WO2016170057A1 (en) | 2015-04-21 | 2016-10-27 | Covestro Deutschland Ag | Solids based on polyisocvanurate polymers produced under adiabatic conditions |
| JP7029295B2 (ja) | 2015-04-21 | 2022-03-03 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | 高い熱安定性を有するポリイソシアヌレートプラスチック |
| JP6266826B1 (ja) * | 2017-04-28 | 2018-01-24 | 大木 彬 | つや消し透明塗料用組成物及びその製造方法 |
| WO2024243374A1 (en) * | 2023-05-24 | 2024-11-28 | Ppg Industries Ohio, Inc. | A coating composition |
| WO2024243377A1 (en) * | 2023-05-24 | 2024-11-28 | Ppg Industries Ohio, Inc. | A coating composition |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4147679A (en) * | 1976-06-02 | 1979-04-03 | Ppg Industries, Inc. | Water-reduced urethane coating compositions |
| DE2829648A1 (de) | 1978-07-06 | 1980-01-24 | Basf Ag | Waessrige ueberzugsmitteldispersion |
| DE3230289A1 (de) * | 1982-08-14 | 1984-02-16 | Bayer Ag, 5090 Leverkusen | Herstellung von pharmazeutischen oder kosmetischen dispersionen |
| DE3313237A1 (de) | 1983-04-13 | 1984-10-18 | Bayer Ag, 5090 Leverkusen | Waessrige, vernetzerhaltige polyurethanzubereitungen und ihre verwendung zur thermoaktiv-einstrich-umkehrbeschichtung |
| DE3345448A1 (de) | 1983-12-15 | 1985-06-27 | Bayer Ag, 5090 Leverkusen | Waessrige polyurethan-einbrennlacke und ihre verwendung zur herstellung von lackfilmen und beschichtungen |
| DE3936288A1 (de) | 1989-11-01 | 1991-05-02 | Bayer Ag | In wasser dispergierbare bindemittelkombinationen, ein verfahren zur herstellung eines einbrennfuellers und dessen verwendung |
| DE4213527A1 (de) | 1992-04-24 | 1993-10-28 | Bayer Ag | Wäßrige Überzugsmittel für elastische Einbrennlackierungen |
| DE4221924A1 (de) * | 1992-07-03 | 1994-01-13 | Bayer Ag | In Wasser lösliche oder dispergierbare Polyisocyanatgemische und ihre Verwendung in Einbrennlacken |
| DE4224617A1 (de) | 1992-07-25 | 1994-01-27 | Herberts Gmbh | Wäßriges Überzugsmittel, Verfahren zu dessen Herstellung und dessen Verwendung bei Verfahren zur Mehrschichtlackierung |
| US5470906A (en) * | 1993-12-27 | 1995-11-28 | The Glidden Company | Odor free, air dry, decorative latex paints |
| US5379947A (en) | 1993-11-09 | 1995-01-10 | Basf Corporation | Process for producing a powder coating composition |
| EP0714958B1 (en) | 1994-11-28 | 1999-10-27 | Basf Corporation | Method for producing fluid powder slurry coating compositions |
| JPH11509563A (ja) | 1995-05-19 | 1999-08-24 | ビーエーエスエフ コーティングス アクチェンゲゼルシャフト | 水性粉末塗料分散液 |
| DE19523084A1 (de) | 1995-06-26 | 1997-04-03 | Basf Lacke & Farben | Wäßrige Pulverlack-Dispersion für Verpackungsbehälter |
| DE19540977A1 (de) | 1995-11-03 | 1997-05-07 | Basf Lacke & Farben | Wäßrige Pulverlack-Dispersionen |
| DE19615116A1 (de) | 1996-04-17 | 1997-10-23 | Bayer Ag | Wäßrige bzw. wasserverdünnbare blockierte Polyisocyanate für die Herstellung von wäßrigen 1K-PUR-Klarlacken mit wesentlich verringerter Thermovergilbung |
| DE19617086A1 (de) * | 1996-04-29 | 1997-10-30 | Bayer Ag | Verfahren zur Herstellung wäßriger Beschichtungsmittel für Einbrennlackierungen |
| US5646213A (en) * | 1996-06-28 | 1997-07-08 | Arco Chemical Technology, L.P. | High-solids and powder coatings from hydroxy-functional acrylic resins |
| DE19708606A1 (de) * | 1997-03-03 | 1998-09-10 | Bayer Ag | Verfahren zur Herstellung von stabilen, feinteiligen Polymerdispersionen |
-
1997
- 1997-08-25 DE DE19736920A patent/DE19736920A1/de not_active Withdrawn
-
1998
- 1998-08-13 DE DE59804030T patent/DE59804030D1/de not_active Expired - Lifetime
- 1998-08-13 ES ES98115241T patent/ES2176872T3/es not_active Expired - Lifetime
- 1998-08-13 PT PT98115241T patent/PT899282E/pt unknown
- 1998-08-13 EP EP98115241A patent/EP0899282B1/de not_active Expired - Lifetime
- 1998-08-13 AT AT98115241T patent/ATE217327T1/de not_active IP Right Cessation
- 1998-08-18 US US09/136,146 patent/US6251985B1/en not_active Expired - Lifetime
- 1998-08-21 CA CA002245447A patent/CA2245447C/en not_active Expired - Fee Related
- 1998-08-24 JP JP10251773A patent/JPH11131017A/ja active Pending
- 1998-08-24 BR BR9803763-3A patent/BR9803763A/pt not_active Application Discontinuation
- 1998-08-24 KR KR1019980034270A patent/KR100571467B1/ko not_active Expired - Fee Related
- 1998-08-25 CZ CZ0270798A patent/CZ296201B6/cs not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CZ296201B6 (cs) | 2006-02-15 |
| US6251985B1 (en) | 2001-06-26 |
| CZ270798A3 (cs) | 1999-03-17 |
| KR19990023822A (ko) | 1999-03-25 |
| JPH11131017A (ja) | 1999-05-18 |
| ES2176872T3 (es) | 2002-12-01 |
| KR100571467B1 (ko) | 2007-01-31 |
| EP0899282A3 (de) | 1999-04-21 |
| PT899282E (pt) | 2002-08-30 |
| EP0899282B1 (de) | 2002-05-08 |
| CA2245447C (en) | 2007-10-30 |
| CA2245447A1 (en) | 1999-02-25 |
| EP0899282A2 (de) | 1999-03-03 |
| BR9803763A (pt) | 1999-12-07 |
| DE59804030D1 (de) | 2002-06-13 |
| ATE217327T1 (de) | 2002-05-15 |
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