DD298119A5 - Estergruppen aufweisende polyisocyanate oder polyisocyanatgemische, ein verfahren zur herstellung derartiger polyisocyanate oder polyisocyanatgemische und ihre verwendung in polyurethanlacken - Google Patents

Estergruppen aufweisende polyisocyanate oder polyisocyanatgemische, ein verfahren zur herstellung derartiger polyisocyanate oder polyisocyanatgemische und ihre verwendung in polyurethanlacken Download PDF

Info

Publication number: DD298119A5
Authority: DD; German Democratic Republic
Prior art keywords: polyisocyanates; polyisocyanate; preparation; polyisocyanate mixtures; functionality
Prior art date: 1989-08-10

Application number

DD90343326A

Other languages

German (de)

English (en)

Inventor

Lutz Schmalstieg

Josef Pedain

Klaus Nachtkamp

Lothar Kahl

Manfred Schoenfelder

Original Assignee

��@��k��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-08-10

Filing date

1990-08-08

Publication date

1992-02-06

1990-08-08 Application filed by ��@��k�� filed Critical ��@��k��

1992-02-06 Publication of DD298119A5 publication Critical patent/DD298119A5/de

Links

239000005056 polyisocyanate Substances 0.000 title claims abstract description 93
229920001228 polyisocyanate Polymers 0.000 title claims abstract description 93
239000000203 mixture Substances 0.000 title claims abstract description 40
238000002360 preparation method Methods 0.000 title claims abstract description 25
238000000034 method Methods 0.000 title claims abstract description 14
239000004814 polyurethane Substances 0.000 title description 4
229920002635 polyurethane Polymers 0.000 title description 4
239000004922 lacquer Substances 0.000 title description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 11
125000004185 ester group Chemical group 0.000 claims abstract description 8
150000002148 esters Chemical class 0.000 claims description 6
150000005846 sugar alcohols Chemical class 0.000 abstract description 18
-1 aliphatic isocyanatocarboxylic acid chlorides Chemical class 0.000 abstract description 9
239000012948 isocyanate Substances 0.000 abstract description 8
150000002513 isocyanates Chemical class 0.000 abstract description 8
235000000346 sugar Nutrition 0.000 abstract description 5
HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 abstract description 4
239000004972 Polyurethane varnish Substances 0.000 abstract description 2
150000008163 sugars Chemical class 0.000 abstract description 2
239000000047 product Substances 0.000 description 17
125000002887 hydroxy group Chemical group [H]O* 0.000 description 13
IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 12
125000001261 isocyanato group Chemical group *N=C=O 0.000 description 11
239000003973 paint Substances 0.000 description 11
150000001298 alcohols Chemical class 0.000 description 10
239000011527 polyurethane coating Substances 0.000 description 9
238000004821 distillation Methods 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
238000006884 silylation reaction Methods 0.000 description 6
239000005051 trimethylchlorosilane Substances 0.000 description 6
229920005862 polyol Polymers 0.000 description 5
150000003077 polyols Chemical class 0.000 description 5
239000005046 Chlorosilane Substances 0.000 description 4
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 4
239000010408 film Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000000376 reactant Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
238000010626 work up procedure Methods 0.000 description 4
KTAVQXDMWKZRKW-UHFFFAOYSA-N 6-isocyanatohexanoyl chloride Chemical compound ClC(=O)CCCCCN=C=O KTAVQXDMWKZRKW-UHFFFAOYSA-N 0.000 description 3
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
238000000576 coating method Methods 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
239000000594 mannitol Substances 0.000 description 3
229920000058 polyacrylate Polymers 0.000 description 3
229920005906 polyester polyol Polymers 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000600 sorbitol Substances 0.000 description 3
PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
229930195725 Mannitol Natural products 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
CGOASDUKZJQFDN-UHFFFAOYSA-N carbonisocyanatidic acid hydrochloride Chemical compound Cl.OC(=O)N=C=O CGOASDUKZJQFDN-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 2
125000005442 diisocyanate group Chemical group 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
239000008103 glucose Substances 0.000 description 2
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
235000010355 mannitol Nutrition 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
238000002103 osmometry Methods 0.000 description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000010409 thin film Substances 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
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
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
NVFNGVSNLHYRSF-UHFFFAOYSA-N 3-isocyanatopropanoyl chloride Chemical compound ClC(=O)CCN=C=O NVFNGVSNLHYRSF-UHFFFAOYSA-N 0.000 description 1
CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 1
OQSLONSLJIOXMY-UHFFFAOYSA-N 4-isocyanatobutanoyl chloride Chemical compound ClC(=O)CCCN=C=O OQSLONSLJIOXMY-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-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
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000007809 chemical reaction catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
239000012971 dimethylpiperazine Substances 0.000 description 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
BKCXNNIZYGZXTB-UHFFFAOYSA-N isocyanoformyl chloride Chemical class ClC(=O)[N+]#[C-] BKCXNNIZYGZXTB-UHFFFAOYSA-N 0.000 description 1
239000008101 lactose Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000000178 monomer Substances 0.000 description 1
VBBUFMFZDHLELS-UHFFFAOYSA-N n-(oxomethylidene)carbamoyl chloride Chemical compound ClC(=O)N=C=O VBBUFMFZDHLELS-UHFFFAOYSA-N 0.000 description 1
150000002917 oxazolidines Chemical class 0.000 description 1
UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
230000019612 pigmentation Effects 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000012262 resinous product Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000004753 textile Substances 0.000 description 1
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
238000005829 trimerization reaction Methods 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000002966 varnish Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
239000011592 zinc chloride 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

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/02—Derivatives of isocyanic acid having isocyanate groups bound to acyclic carbon atoms
- C07C265/04—Derivatives of isocyanic acid having isocyanate groups bound to acyclic carbon atoms of a saturated carbon skeleton
- 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
- C08G18/771—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur oxygen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Biochemistry (AREA)
Biotechnology (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Molecular Biology (AREA)
Polyurethanes Or Polyureas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Paints Or Removers (AREA)

DD90343326A 1989-08-10 1990-08-08 Estergruppen aufweisende polyisocyanate oder polyisocyanatgemische, ein verfahren zur herstellung derartiger polyisocyanate oder polyisocyanatgemische und ihre verwendung in polyurethanlacken DD298119A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3926389A DE3926389A1 (de)	1989-08-10	1989-08-10	Estergruppen aufweisende polyisocyanate oder polyisocyanatgemische, ein verfahren zur herstellung derartiger polyisocyanate oder polyisocyanatgemische und ihre verwendung in polyurethanlacken

Publications (1)

Publication Number	Publication Date
DD298119A5 true DD298119A5 (de)	1992-02-06

Family

ID=6386832

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD90343326A DD298119A5 (de)	1989-08-10	1990-08-08	Estergruppen aufweisende polyisocyanate oder polyisocyanatgemische, ein verfahren zur herstellung derartiger polyisocyanate oder polyisocyanatgemische und ihre verwendung in polyurethanlacken

Country Status (9)

Country	Link
US (1)	US5096994A (ja)
EP (1)	EP0412380B1 (ja)
JP (1)	JP2936495B2 (ja)
KR (1)	KR0163428B1 (ja)
AT (1)	ATE96425T1 (ja)
CA (1)	CA2021716C (ja)
DD (1)	DD298119A5 (ja)
DE (2)	DE3926389A1 (ja)
ES (1)	ES2059925T3 (ja)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE69325358T2 (de) *	1992-12-14	2000-01-13	General Electric Co., Schenectady	Isocyanatgruppen-haltige Siloxan-Copolymere
US6395860B1 (en)	2000-09-26	2002-05-28	Basf Corporation	Clearcoat composition with improved scratch and mar resistance
WO2016162394A1 (de)	2015-04-07	2016-10-13	Covestro Deutschland Ag	Verfahren zum verkleben von substraten mit klebstoffen

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1269585A (en) *	1969-03-15	1972-04-06	Bayer Ag	A process for the preparation of ester isocyanates
DE2120090A1 (de) *	1971-04-24	1972-11-09	Bayer Ag	Neue Hilfsstoffe zur Ausrüstung von Keratinfasern enthaltenden Textilien
DE2308015B2 (de) *	1973-02-17	1980-07-31	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung von Polyisocyanaten mit Biuretstruktur
DE3432081A1 (de) *	1984-08-31	1986-03-06	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von oligomeren polyisocyanaten und ihre verwendung bei der herstellung von polyurethankunststoffen
DE3634248A1 (de) *	1986-10-08	1988-04-21	Bayer Ag	Verfahren zur herstellung von isocyanaten
GB2203159B (en) *	1987-04-03	1990-12-12	Asahi Chemical Ind	An isocyanurate polyisocyanate and its use as a curing agent for a two-component polyurethane composition
DE3730986A1 (de) *	1987-09-16	1989-03-30	Bayer Ag	Verfahren zur herstellung von isocyanaten und ihre verwendung zur herstellung von estergruppen aufweisenden polyisocyanaten

1989
- 1989-08-10 DE DE3926389A patent/DE3926389A1/de not_active Withdrawn
1990
- 1990-07-20 CA CA002021716A patent/CA2021716C/en not_active Expired - Fee Related
- 1990-07-28 DE DE90114531T patent/DE59003207D1/de not_active Expired - Fee Related
- 1990-07-28 AT AT90114531T patent/ATE96425T1/de not_active IP Right Cessation
- 1990-07-28 EP EP90114531A patent/EP0412380B1/de not_active Expired - Lifetime
- 1990-07-28 ES ES90114531T patent/ES2059925T3/es not_active Expired - Lifetime
- 1990-08-02 US US07/561,770 patent/US5096994A/en not_active Expired - Lifetime
- 1990-08-08 KR KR1019900012126A patent/KR0163428B1/ko not_active Expired - Fee Related
- 1990-08-08 DD DD90343326A patent/DD298119A5/de not_active IP Right Cessation
- 1990-08-08 JP JP2208328A patent/JP2936495B2/ja not_active Expired - Fee Related

Also Published As

Publication number	Publication date
KR0163428B1 (ko)	1999-01-15
DE3926389A1 (de)	1991-02-14
JP2936495B2 (ja)	1999-08-23
EP0412380B1 (de)	1993-10-27
KR910004696A (ko)	1991-03-29
US5096994A (en)	1992-03-17
ES2059925T3 (es)	1994-11-16
JPH03218344A (ja)	1991-09-25
CA2021716A1 (en)	1991-02-11
CA2021716C (en)	1999-12-28
DE59003207D1 (de)	1993-12-02
ATE96425T1 (de)	1993-11-15
EP0412380A1 (de)	1991-02-13

Legal Events

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2000-06-08	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0339396B1 (de)	1992-03-11	Verfahren zur Herstellung von Isocyanuratgruppen aufweisenden Polyisocyanaten
DE69527430T2 (de)	2003-02-20	Uretdion- und allophanatgruppen aufweisende polyisocyanate
EP0712840B1 (de)	1999-03-03	Allophanatgruppen aufweisende Polyisocyanate
DE69524508T2 (de)	2002-05-29	Niedrige Oberflächenenergie aufweisende Polyisocyanate, sowie ihre Verwendung in Einkomponent- oder Zweikomponenten-Beschichtungszusammensetzungen
EP0649866A1 (de)	1995-04-26	Lackpolyisocyanate und ihre Verwendung
WO2007039133A1 (de)	2007-04-12	Zweikomponenten-systeme für die herstellung flexibler beschichtungen
DE4140660A1 (de)	1993-06-17	Ether- und urethangruppen aufweisende polyisocyanate, ein verfahren zu ihrer herstellung und ihrer verwendung
EP3271411A1 (de)	2018-01-24	Silangruppen enthaltende polyisocyanate auf basis von 1,5-diisocyanatopentan
WO2004005363A1 (de)	2004-01-15	Uretdiongruppen enthaltende polyadditionsprodukte
EP0010248A1 (de)	1980-04-30	Isocyanatgemisch und seine Verwendung als Bindemittel in Einkomponenten-Lacken
DE60100584T2 (de)	2004-06-24	Hydroxyfunktionelle Urethane mit einer tertiären Carbamat-Bindung
EP1735363B1 (de)	2008-01-02	Verfärbungsstabile polyetherallophanate
DE3507719A1 (de)	1986-09-11	Isocyanuratgruppen aufweisende polyisocyanate, ein verfahren zu ihrer herstellung und ihre verwendung als isocyanatkomponente in polyurethanlacken
DE69727741T2 (de)	2005-01-13	Niedrigviskose Polyisocyanate hergestellt aus monomeren Triisocyanaten
DE3133865C2 (de)	1983-12-01	Verfahren zur Herstellung einer organischen Polyisocyanat-Zusammensetzung sowie deren Verwendung
DE69626733T2 (de)	2003-09-18	Allophanatgruppen und gegebenenfalls Isocyanuratgruppen aufweisende Polyisocyanate
EP0412380B1 (de)	1993-10-27	Estergruppen aufweisende Polyisocyanate oder Polyisocyanatgemische, ein Verfahren zur Herstellung derartiger Polyisocyanate oder Polyisocyanatgemische und ihre Verwendung in Polyurethanlacken
EP1669384B1 (de)	2009-09-02	BOE- und/oder Polyorthoestergruppenhaltige Bindemittelgemische
EP0727453B1 (de)	1998-05-20	Isocyanurat-Polyisocyanate auf Basis von 1,3-Diisocyanatocycloalkanen
EP0132514B1 (de)	1987-07-08	Feuchtigkeitshärtende Lacke auf Isocyanatharz-Basis
DE3018198A1 (de)	1981-11-19	Neue isocyanato-isocyanurate, ein verfahren zu ihrer herstellung, sowie ihre verwendung als isocyanat-komponente in polyurethan-lacken
DE10300155A1 (de)	2004-07-15	Neue Beschichtungssysteme
JPS63454B2 (ja)	1988-01-07
DD297981A5 (de)	1992-01-30	Verfahren zur herstellung von ester- und isocyanatgruppen aufweisenden prepolymeren und ihre verwendung aks bindemittel
DD151466A1 (de)	1981-10-21	Verfahren zur herstellung lagerstabiler polyurethan-einkomponentenlacke