JPH1046055A - 焼付温度が低い粉体被覆組成物 - Google Patents
焼付温度が低い粉体被覆組成物Info
- Publication number
- JPH1046055A JPH1046055A JP9118621A JP11862197A JPH1046055A JP H1046055 A JPH1046055 A JP H1046055A JP 9118621 A JP9118621 A JP 9118621A JP 11862197 A JP11862197 A JP 11862197A JP H1046055 A JPH1046055 A JP H1046055A
- Authority
- JP
- Japan
- Prior art keywords
- component
- weight
- coating composition
- molecular weight
- powder coating
- 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.)
- Pending
Links
- 239000008199 coating composition Substances 0.000 title claims abstract description 63
- 239000000843 powder Substances 0.000 title claims abstract description 60
- 239000003054 catalyst Substances 0.000 claims abstract description 42
- 150000001875 compounds Chemical class 0.000 claims abstract description 41
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000004814 polyurethane Substances 0.000 claims abstract description 25
- 229920002635 polyurethane Polymers 0.000 claims abstract description 25
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 24
- 239000007787 solid Substances 0.000 claims abstract description 21
- 239000007788 liquid Substances 0.000 claims abstract description 17
- 125000000320 amidine group Chemical group 0.000 claims abstract description 14
- 239000011230 binding agent Substances 0.000 claims abstract description 12
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 10
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical group O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims description 40
- 229910052757 nitrogen Inorganic materials 0.000 claims description 28
- 125000005587 carbonate group Chemical group 0.000 claims description 12
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 11
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims description 10
- 125000005442 diisocyanate group Chemical group 0.000 claims description 10
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 8
- 238000004364 calculation method Methods 0.000 claims description 5
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000203 mixture Substances 0.000 abstract description 15
- 239000012948 isocyanate Substances 0.000 abstract description 3
- 150000002513 isocyanates Chemical class 0.000 abstract description 3
- 239000000758 substrate Substances 0.000 abstract description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 37
- 239000011248 coating agent Substances 0.000 description 24
- 150000001409 amidines Chemical class 0.000 description 16
- 229920000728 polyester Polymers 0.000 description 11
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000010409 thin film Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- -1 bicyclic amidines Chemical class 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 3
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- JQZRVMZHTADUSY-UHFFFAOYSA-L di(octanoyloxy)tin Chemical compound [Sn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O JQZRVMZHTADUSY-UHFFFAOYSA-L 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 238000004455 differential thermal analysis Methods 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 238000010494 dissociation reaction Methods 0.000 description 3
- 230000005593 dissociations Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 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
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000007373 indentation Methods 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 description 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 1
- WOFPPJOZXUTRAU-UHFFFAOYSA-N 2-Ethyl-1-hexanol Natural products CCCCC(O)CCC WOFPPJOZXUTRAU-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- FEJIGNDKURQIRD-UHFFFAOYSA-N 2-methyl-1,2,3,4-tetrahydropyrimidine Chemical class CC1NCC=CN1 FEJIGNDKURQIRD-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- BHCFVCRRNLIOGM-UHFFFAOYSA-J C(CO)(=O)[O-].[Mo+4].C(CO)(=O)[O-].C(CO)(=O)[O-].C(CO)(=O)[O-] Chemical compound C(CO)(=O)[O-].[Mo+4].C(CO)(=O)[O-].C(CO)(=O)[O-].C(CO)(=O)[O-] BHCFVCRRNLIOGM-UHFFFAOYSA-J 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000004729 acetoacetic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
- UMXYJWSQJORGEM-UHFFFAOYSA-N ethene;piperazine Chemical compound C=C.C1CNCCN1 UMXYJWSQJORGEM-UHFFFAOYSA-N 0.000 description 1
- PLONEVHFXDFSLA-UHFFFAOYSA-N ethyl hexanoate;tin(2+) Chemical compound [Sn+2].CCCCCC(=O)OCC PLONEVHFXDFSLA-UHFFFAOYSA-N 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- DMNYJSMNRDYEOT-UHFFFAOYSA-N n,n,n'-trimethylmethanimidamide Chemical compound CN=CN(C)C DMNYJSMNRDYEOT-UHFFFAOYSA-N 0.000 description 1
- SRPCLECGIYMIMN-UHFFFAOYSA-N n,n-dimethyl-n'-phenylmethanimidamide Chemical compound CN(C)C=NC1=CC=CC=C1 SRPCLECGIYMIMN-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- PRVDZBGQJZSFNF-UHFFFAOYSA-N nonyl phenyl hydrogen phosphite Chemical compound CCCCCCCCCOP(O)OC1=CC=CC=C1 PRVDZBGQJZSFNF-UHFFFAOYSA-N 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
- C08G18/798—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing urethdione 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
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/1858—Catalysts containing secondary or tertiary amines or salts thereof having carbon-to-nitrogen double bonds
-
- 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
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/20—Heterocyclic amines; Salts thereof
- C08G18/2045—Heterocyclic amines; Salts thereof containing condensed heterocyclic rings
- C08G18/2063—Heterocyclic amines; Salts thereof containing condensed heterocyclic rings having two nitrogen atoms in the condensed ring system
-
- 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
- C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
- C08G18/4219—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from aromatic dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
-
- 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
- C08G18/8003—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
- C08G18/8006—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32
- C08G18/8009—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203
- C08G18/8012—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203 with diols
- C08G18/8016—Masked aliphatic or cycloaliphatic 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
- C08G2150/00—Compositions for coatings
- C08G2150/20—Compositions for powder coatings
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19616496.6 | 1996-04-25 | ||
| DE19616496A DE19616496A1 (de) | 1996-04-25 | 1996-04-25 | Abspaltfreier Polyurethan-Pulverlack mit niedriger Einbrenntemperatur |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH1046055A true JPH1046055A (ja) | 1998-02-17 |
| JPH1046055A5 JPH1046055A5 (enExample) | 2005-03-17 |
Family
ID=7792397
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9118621A Pending JPH1046055A (ja) | 1996-04-25 | 1997-04-23 | 焼付温度が低い粉体被覆組成物 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5847044A (enExample) |
| EP (1) | EP0803524B1 (enExample) |
| JP (1) | JPH1046055A (enExample) |
| AT (1) | ATE255135T1 (enExample) |
| CA (1) | CA2203229C (enExample) |
| DE (2) | DE19616496A1 (enExample) |
| DK (1) | DK0803524T3 (enExample) |
| ES (1) | ES2210410T3 (enExample) |
| NO (1) | NO313757B1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001114855A (ja) * | 1999-09-09 | 2001-04-24 | Bayer Ag | ウレトジオン基および遊離イソシアネート基を含有する高官能性粉末コーティング用架橋剤 |
| JP2001152079A (ja) * | 1999-11-24 | 2001-06-05 | Kansai Paint Co Ltd | 熱硬化型粉体塗料 |
| JP2004331952A (ja) * | 2003-05-03 | 2004-11-25 | Degussa Ag | 高反応性ポリウレタン粉末塗料組成物、その製造方法、該組成物のための効果触媒、粉末塗料被覆層の製造のための粉末塗料硬化剤、ポリマー及び触媒の使用並びに被覆組成物 |
Families Citing this family (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6255523B1 (en) | 1998-09-18 | 2001-07-03 | Mcwhorter Technologies, Inc. | Power coatings based on branched oligoesters and non-emissive uretdione polyisocyanates |
| DE19856878A1 (de) * | 1998-12-10 | 2000-06-15 | Inst Polymerforschung Dresden | Härtbare uretdiongruppenhaltige Massen und ein Verfahren zu ihrer Herstellung und Verarbeitung sowie ihre Verwendung |
| US6228472B1 (en) | 1998-12-21 | 2001-05-08 | Basf Corporation | Process for synthesis of allophanate compounds and compositions including the product thereof |
| US6214470B1 (en) | 1998-12-21 | 2001-04-10 | Basf Corporation | Cathodic electrocoat composition |
| DE19903710A1 (de) * | 1999-01-30 | 2000-08-03 | Bayer Ag | Uretdiongruppen und freie Isocyanatgruppen aufweisende Pulverlackvernetzer |
| DE10031987A1 (de) * | 2000-06-30 | 2002-01-24 | Basf Coatings Ag | Mit Propargylalkohol blockierte Polyisocyanate, Verfahren zu ihrer Herstellung und ihre Verwendung |
| ES2257369T3 (es) * | 2000-10-13 | 2006-08-01 | Tosoh Corporation | Catalizador para la preparacion de una composicion sellante de dos componentes a base de poliuretano. |
| DE60206669T2 (de) * | 2001-02-06 | 2006-07-06 | Dainippon Ink And Chemicals, Inc. | Harzzusammensetzung für Pulverbeschichtung, Pulverbeschichtung und beschichtete Gegenstände |
| DE10260300A1 (de) * | 2002-12-20 | 2004-07-01 | Bayer Ag | Abspalterfreie Pulverlackvernetzer |
| DE10320267A1 (de) * | 2003-05-03 | 2004-11-18 | Degussa Ag | Bei niedriger Temperatur härtbare feste uretdiongruppenhaltige Polyurethan-Pulverlackzusammensetzungen |
| DE10346957A1 (de) * | 2003-10-09 | 2005-05-04 | Degussa | Hochreaktive, flüssige uretdiongruppenhaltige Polyurenthansysteme, die bei niedriger Temperatur härtbar sind |
| DE10346958A1 (de) | 2003-10-09 | 2005-05-12 | Degussa | Uretdiongruppenhaltige Polyurethanzusammensetzungen, welche bei niedriger Temperatur härtbar sind |
| DE10347902A1 (de) * | 2003-10-15 | 2005-05-19 | Degussa Ag | Feste uretdiongruppenhaltige Polyadditionsverbindungen |
| DE102004017005A1 (de) * | 2004-04-02 | 2005-10-20 | Bayer Materialscience Ag | Abspalterfreier Polyurethan-Pulverlack mit niedriger Einbrenntemperatur |
| DE102004020451A1 (de) * | 2004-04-27 | 2005-12-01 | Degussa Ag | Uretdiongruppenhaltige Polyurethanzusammensetzungen, welche bei niedriger Temperatur härtbar sind und (teil-)kristalline Harze enthalten |
| DE102004020429A1 (de) * | 2004-04-27 | 2005-11-24 | Degussa Ag | Uretdiongruppenhaltige Polyurethanzusammensetzungen, welche bei niedriger Temperatur härtbar sind und (teil-)kristalline Harze enthalten |
| US7485729B2 (en) | 2004-08-12 | 2009-02-03 | King Industries, Inc. | Organometallic compositions and coating compositions |
| US20060036007A1 (en) * | 2004-08-12 | 2006-02-16 | King Industries, Inc. | Organometallic compositions and coating compositions |
| DE102005013329A1 (de) * | 2005-03-23 | 2006-11-16 | Degussa Ag | Niedrigviskose uretdiongruppenhaltige Polyadditionsverbindungen, Verfahren zur Herstellung und Verwendung |
| DE102005060828A1 (de) | 2005-12-20 | 2007-06-28 | Bayer Materialscience Ag | Verfahren zur Herstellung von Polyadditionsverbindungen |
| DE102006045003A1 (de) * | 2006-09-23 | 2008-03-27 | Bayer Materialscience Ag | Polyurethan-Pulverlack |
| DE102007022789A1 (de) | 2007-04-26 | 2008-10-30 | Evonik Degussa Gmbh | Bei niedriger Temperatur härtbare, Uretdiongruppen aufweisende Polyurethanzusammensetzungen enthaltend Polymere auf der Basis von sekundären OH-Gruppen tragenden Polyolen |
| DE102007057057A1 (de) | 2007-11-27 | 2009-05-28 | Evonik Degussa Gmbh | Uretdiongruppen haltige Polyurethanzusammensetzungen, welche bei niedriger Temperatur härtbar sind und haftungsverbessernde Harze enthalten |
| US20100227942A1 (en) | 2007-12-18 | 2010-09-09 | Emmanouil Spyrou | Dual-cure formulations with components containing uretdione groups |
| DE102008007386A1 (de) | 2008-02-01 | 2009-08-06 | Evonik Degussa Gmbh | Verfahren zur Herstellung hochreaktiver uretdiongruppenhaltiger Polyurethanzusammensetzungen im Dryblend |
| DE102008002703A1 (de) | 2008-06-27 | 2009-12-31 | Evonik Degussa Gmbh | Hochreaktive, Uretdiongruppen haltige Polyurethanzusammensetzungen, die metallfreie Acetylacetonate enthalten |
| DE102009028862A1 (de) | 2008-12-22 | 2010-07-01 | Evonik Degussa Gmbh | Monomerarme 1 : 1 Monoaddukte aus reaktiven olefinischen Verbindungen und Diisocyanaten unter Verwendung einbaubarer Inhibitoren |
| DE102009001793A1 (de) | 2009-03-24 | 2010-10-07 | Evonik Degussa Gmbh | Prepregs und daraus hergestellte Formkörper |
| DE102009001806A1 (de) | 2009-03-24 | 2010-09-30 | Evonik Degussa Gmbh | Prepregs und daraus bei niedriger Temperatur hergestellte Formkörper |
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| DE102010041239A1 (de) | 2010-09-23 | 2012-03-29 | Evonik Degussa Gmbh | Prepregs auf der Basis lagerstabiler reaktiven oder hochreaktiven Polyurethanzusammensetzung |
| DE102010041256A1 (de) | 2010-09-23 | 2012-03-29 | Evonik Degussa Gmbh | Prepregs auf der Basis lagerstabiler reaktiven oder hochreaktiven Polyurethanzusammensetzung mit fixierter Folie sowie die daraus hergestellten Composite-Bauteil |
| WO2012093006A1 (de) | 2011-01-04 | 2012-07-12 | Evonik Degussa Gmbh | Composite-halbzeuge und daraus hergestellte formteile sowie direkt hergestellte formteile auf basis von hydroxyfunktionalisierten (meth) acrylaten, die mittels uretdionen duroplastisch vernetzt werden |
| EP2683767A1 (en) | 2011-03-06 | 2014-01-15 | King Industries, Inc. | Compositions of a metal amidine complex and second compound, coating compositions comprising same |
| EP2686360B1 (de) | 2011-03-14 | 2016-10-12 | BASF Coatings GmbH | Polyurethan-beschichtungsmittelzusammensetzung, mehrstufige beschichtungsverfahren unter verwendung dieser beschichtungsmittelzusammensetzungen sowie die verwendung der beschichtungsmittelzusammensetzung als klarlack und pigmentierter lack bzw. anwendung des beschichtungsverfahrens für die automobilreparaturlackierung und/oder für die beschichtung von kunststoffsubstraten und/oder nutzfahrzeugen |
| PL2686361T3 (pl) | 2011-03-14 | 2015-04-30 | Basf Coatings Gmbh | Poliuretanowa kompozycja środków powłokowych, wieloetapowe sposoby powlekania przy użyciu tych kompozycji środków powłokowych oraz zastosowanie kompozycji środków powłokowych jako lakieru bezbarwnego i lakieru pigmentowanego lub zastosowanie sposobu powlekania do renowacyjnego lakierowania samochodów i/lub do powlekania podłoży z tworzywa sztucznego i/lub pojazdów użytkowych |
| US9139751B2 (en) | 2011-03-14 | 2015-09-22 | Basf Coatings Gmbh | Polyurethane coating material composition, multistage coating methods using these coating material compositions, and also the use of the coating material composition as clearcoat material and pigmented coating material, and application of the coating method for automotive refinish and/or for the coating of plastics substrates and/or of utility vehicles |
| DE102011006163A1 (de) | 2011-03-25 | 2012-09-27 | Evonik Degussa Gmbh | Lagerstabile Polyurethan-Prepregs und daraus hergestellte Formkörper aus Polyurethanzusammensetzung mit flüssigen Harzkomponenten |
| EP2877507A1 (de) | 2012-07-27 | 2015-06-03 | Bayer Materialscience AG | Klebstoff-formulierungen |
| DE102012218081A1 (de) | 2012-10-04 | 2014-04-10 | Evonik Industries Ag | Neuartige hydrophile Polyisocyanate mit verbesserter Lagerstabilität |
| DE102013204124A1 (de) | 2013-03-11 | 2014-09-11 | Evonik Industries Ag | Composite-Halbzeuge und daraus hergestellte Formteile sowie direkt hergestellte Formteile auf Basis von hydroxyfunktionalisierten (Meth)Acrylaten und Uretdionen die mittels Strahlung duroplastisch vernetzt werden |
| DE102013220239A1 (de) | 2013-10-08 | 2015-04-23 | Evonik Industries Ag | Polyfunktionelle Urethan(meth)acrylate aus Monomer armen Diisocyanat-Monoaddukten |
| DE102014209183A1 (de) | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Reaktive Zusammensetzung aus einer Uretdiongruppen haltigen Dispersion und Polyaminen |
| DE102014214130A1 (de) | 2014-07-21 | 2016-01-21 | Evonik Degussa Gmbh | Hochreaktive, Uretdiongruppen haltige Polyurethanzusammensetzungen, die Carbonatsalze enthalten |
| EP2993202A1 (de) | 2014-09-08 | 2016-03-09 | Evonik Degussa GmbH | Composite-Halbzeuge und daraus hergestellte Formteile sowie direkt hergestellte Formteile auf Basis von hydroxyfunktionalisierten (Meth)Acrylaten und Uretdionen, die duroplastisch vernetzt werden |
| EP3184567A1 (de) | 2015-12-21 | 2017-06-28 | Evonik Degussa GmbH | Acrylatterminierte urethanpolybutadiene aus monomerarmen 1:1 monoaddukten aus reaktiven olfinischen verbindungen und diisocyanaten und hydroxyterminierten polybutadienen |
| EP3184568A1 (en) | 2015-12-21 | 2017-06-28 | Evonik Degussa GmbH | Acrylate-terminated urethane polybutadienes from low-monomer 1:1 monoadductes from reactive olefinic compounds and diisocyanates and hydroxy-terminated polybutadienes for liquid optically clear adhesives (locas) |
| PL238230B1 (pl) | 2016-09-20 | 2021-07-26 | Politechnika Rzeszowska Im Ignacego Lukasiewicza | Blokowane poliizocyjaniany, sposób ich wytwarzania i zastosowanie |
| ES2880621T3 (es) | 2016-12-02 | 2021-11-25 | Evonik Degussa Gmbh | Productos preimpregnados de poliuretano 1K estables al almacenamiento y cuerpos moldeados a partir de la composición de poliuretano producidos a partir de estos |
| EP3765544A1 (en) | 2018-03-16 | 2021-01-20 | 3M Innovative Properties Company | Compositions, method of bonding, and assembly |
| WO2019175709A1 (en) | 2018-03-16 | 2019-09-19 | 3M Innovative Properties Company | Compositions, method of bonding, and bonded assembly |
| EP3543270A1 (de) | 2018-03-23 | 2019-09-25 | Covestro Deutschland AG | Katalysatorsystem für uretdiondispersionen |
| WO2019183330A1 (en) | 2018-03-23 | 2019-09-26 | Covestro Llc | Basecoat acid neutralization through inorganic salts |
| EP3572446A1 (de) | 2018-05-24 | 2019-11-27 | Evonik Degussa GmbH | Reaktive mischung von uretdionen und katalysatoren |
| WO2020065456A1 (en) | 2018-09-25 | 2020-04-02 | 3M Innovative Properties Company | One-part thermally curable composition |
| EP3656798A1 (de) | 2018-11-23 | 2020-05-27 | Evonik Operations GmbH | Niedrigviskose nco-prepolymere mit geringem rest-monomergehalt |
| EP3763762A1 (de) | 2019-07-11 | 2021-01-13 | Covestro Intellectual Property GmbH & Co. KG | Polyuretdion-pulverlack |
| US20220251280A1 (en) | 2019-07-11 | 2022-08-11 | Covestro Intellectual Property Gmbh & Co. Kg | Process of preparing allophanate- and/or thioallophanate group-containing compounds |
| EP3872108A1 (de) | 2020-02-28 | 2021-09-01 | Covestro Intellectual Property GmbH & Co. KG | Uretdiongruppen enthaltende zusammensetzungen |
| EP3916032A1 (de) | 2020-05-29 | 2021-12-01 | Covestro Deutschland AG | Bei niedrigen temperaturen vernetzende uretdiongruppen enthaltende zusammensetzungen |
| EP3929233A1 (de) | 2020-06-25 | 2021-12-29 | Evonik Operations GmbH | Reaktive polyurethan-zusammensetzungen |
| EP4029892A1 (de) | 2021-01-13 | 2022-07-20 | Covestro Deutschland AG | Uretdiongruppen enthaltende zusammensetzungen |
| US20240343941A1 (en) | 2021-08-02 | 2024-10-17 | Basf Se | Dual-cure resin composition comprising uretdione-containing compound and its use in 3d printing |
| WO2024033289A1 (en) | 2022-08-12 | 2024-02-15 | Basf Se | A photocurable oligomer containing uretdione groups, method of preparing the oligomer and dual-cure resin composition containing the oligomer thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1542058A (fr) * | 1966-10-29 | 1968-10-11 | San Abbott Ltd | Procédé de préparation de polyuréthanes à partir d'isocyanates et de polyols à l'aide de diazabicycloalkènes comme catalyseurs |
| DE2312391A1 (de) * | 1973-03-13 | 1974-09-19 | Bayer Ag | Pulverfoermige, vernetzbare ueberzugsmittel |
| DE2420475A1 (de) * | 1974-04-27 | 1975-11-06 | Bayer Ag | Uretdiongruppen aufweisende polyadditionsprodukte |
| DE2502934A1 (de) * | 1975-01-24 | 1976-07-29 | Bayer Ag | Uretdiongruppen und endstaendige blockierte isocyanatgruppen aufweisende organische verbindungen |
| DE2722514C2 (de) * | 1977-05-18 | 1982-10-14 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Harnstoffengruppen aufweisenden hochmolekularen Verbindungen |
| DE3030539A1 (de) * | 1980-08-13 | 1982-04-01 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von abspaltfreien polyurethan-pulverlacken sowie die danach hergestellten lacke |
| DE3030588A1 (de) * | 1980-08-13 | 1982-03-18 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von blockierungsmittelfreien polyurethan-pulverlacken mit hoher lagerstabilitaet, die oberhalb 120(grad) c haertbar sind, sowie die danach hergestellten polyurethan-pulverlacke |
| DE3030572A1 (de) * | 1980-08-13 | 1982-03-18 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von uretdiongruppenhaltigen polyadditionsprodukten sowie die danach hergestellten produkte |
| DE3403499A1 (de) * | 1984-02-02 | 1985-08-08 | Bayer Ag, 5090 Leverkusen | Verwendung von hitzehaertbaren polyurethanharnstoff-reaktiv-klebstoffmassen |
| DE3624775A1 (de) * | 1986-07-22 | 1988-01-28 | Bayer Ag | Pulverlack und seine verwendung zur beschichtung von hitzeresistenten substraten |
| WO1991007452A1 (en) * | 1989-11-20 | 1991-05-30 | Eastman Kodak Company | Powder coating compositions |
| CA2115763A1 (en) * | 1991-08-27 | 1993-03-04 | Robert B. Barbee | Thermosetting powder coating compositions |
| DE4327573A1 (de) * | 1993-08-17 | 1995-02-23 | Bayer Ag | Uretdion-Pulverlackvernetzer mit niedriger Schmelzviskosität |
| DE4337855A1 (de) * | 1993-11-05 | 1995-05-11 | Bayer Ag | Pulverlack und seine Verwendung |
-
1996
- 1996-04-25 DE DE19616496A patent/DE19616496A1/de not_active Withdrawn
-
1997
- 1997-04-03 US US08/834,799 patent/US5847044A/en not_active Expired - Fee Related
- 1997-04-14 EP EP97106063A patent/EP0803524B1/de not_active Expired - Lifetime
- 1997-04-14 DK DK97106063T patent/DK0803524T3/da active
- 1997-04-14 DE DE59711041T patent/DE59711041D1/de not_active Expired - Lifetime
- 1997-04-14 AT AT97106063T patent/ATE255135T1/de not_active IP Right Cessation
- 1997-04-14 ES ES97106063T patent/ES2210410T3/es not_active Expired - Lifetime
- 1997-04-21 CA CA002203229A patent/CA2203229C/en not_active Expired - Fee Related
- 1997-04-23 JP JP9118621A patent/JPH1046055A/ja active Pending
- 1997-04-24 NO NO19971886A patent/NO313757B1/no not_active IP Right Cessation
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001114855A (ja) * | 1999-09-09 | 2001-04-24 | Bayer Ag | ウレトジオン基および遊離イソシアネート基を含有する高官能性粉末コーティング用架橋剤 |
| JP2001152079A (ja) * | 1999-11-24 | 2001-06-05 | Kansai Paint Co Ltd | 熱硬化型粉体塗料 |
| JP2004331952A (ja) * | 2003-05-03 | 2004-11-25 | Degussa Ag | 高反応性ポリウレタン粉末塗料組成物、その製造方法、該組成物のための効果触媒、粉末塗料被覆層の製造のための粉末塗料硬化剤、ポリマー及び触媒の使用並びに被覆組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE19616496A1 (de) | 1997-10-30 |
| ATE255135T1 (de) | 2003-12-15 |
| EP0803524B1 (de) | 2003-11-26 |
| NO971886L (no) | 1997-10-27 |
| US5847044A (en) | 1998-12-08 |
| DE59711041D1 (de) | 2004-01-08 |
| EP0803524A1 (de) | 1997-10-29 |
| CA2203229C (en) | 2005-06-21 |
| NO313757B1 (no) | 2002-11-25 |
| ES2210410T3 (es) | 2004-07-01 |
| CA2203229A1 (en) | 1997-10-25 |
| DK0803524T3 (da) | 2004-03-08 |
| NO971886D0 (no) | 1997-04-24 |
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