JP2009062533A5 - - Google Patents

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Publication number: JP2009062533A5
Authority: JP; Japan
Prior art keywords: optionally; radiation; group; compound; mol
Prior art date: 2008-08-25
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.): Granted

Application number

JP2008215334A

Other languages

English (en)

Japanese (ja)

Other versions

JP2009062533A (ja

JP5591458B2 (ja

Filing date

2008-08-25

Publication date

2011-10-06

2007-08-25 Priority claimed from DE102007040239A external-priority patent/DE102007040239A1/de

2008-08-25 Application filed filed Critical

2009-03-26 Publication of JP2009062533A publication Critical patent/JP2009062533A/ja

2011-10-06 Publication of JP2009062533A5 publication Critical patent/JP2009062533A5/ja

2014-09-17 Application granted granted Critical

2014-09-17 Publication of JP5591458B2 publication Critical patent/JP5591458B2/ja

Status Expired - Fee Related legal-status Critical Current

2028-08-25 Anticipated expiration legal-status Critical

Links

150000001875 compounds Chemical class 0.000 claims description 16
230000005855 radiation Effects 0.000 claims description 11
238000000576 coating method Methods 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 8
238000000034 method Methods 0.000 claims description 7
AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 6
239000011248 coating agent Substances 0.000 claims description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 4
238000006116 polymerization reaction Methods 0.000 claims description 4
239000003054 catalyst Substances 0.000 claims description 3
239000003999 initiator Substances 0.000 claims description 3
239000000463 material Substances 0.000 claims description 3
239000003973 paint Substances 0.000 claims description 3
229920001228 polyisocyanate Polymers 0.000 claims description 3
239000005056 polyisocyanate Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
239000008199 coating composition Substances 0.000 claims description 2
238000009472 formulation Methods 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
239000000976 ink Substances 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 6
QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims 4
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 2
239000000853 adhesive Substances 0.000 claims 1
230000001070 adhesive effect Effects 0.000 claims 1
238000005266 casting Methods 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 claims 1
239000000805 composite resin Substances 0.000 claims 1
239000000178 monomer Substances 0.000 claims 1
229920002120 photoresistant polymer Polymers 0.000 claims 1
239000011347 resin Substances 0.000 claims 1
229920005989 resin Polymers 0.000 claims 1
239000000565 sealant Substances 0.000 claims 1
238000004513 sizing Methods 0.000 claims 1
150000003512 tertiary amines Chemical class 0.000 claims 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
150000001298 alcohols Chemical class 0.000 description 8
150000002009 diols Chemical class 0.000 description 5
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
-1 polybutylene Polymers 0.000 description 4
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000001723 curing Methods 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 2
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
239000004146 Propane-1,2-diol Substances 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
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
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
239000004417 polycarbonate Substances 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
229960004063 propylene glycol Drugs 0.000 description 2
235000013772 propylene glycol Nutrition 0.000 description 2
IUYYVMKHUXDWEU-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,1-diol Chemical compound CC(C)CC(C)(C)C(O)O IUYYVMKHUXDWEU-UHFFFAOYSA-N 0.000 description 1
WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 1
IUGOPULVANEDRX-UHFFFAOYSA-N 2-ethylhexane-1,1-diol Chemical compound CCCCC(CC)C(O)O IUGOPULVANEDRX-UHFFFAOYSA-N 0.000 description 1
QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
238000003848 UV Light-Curing Methods 0.000 description 1
239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
FGUUNXDRMVKHCF-UHFFFAOYSA-N bis(hydroxymethyl)tricyclo[5.2.1.0(2,6)]decane Chemical compound C12CCCC2(CO)C2(CO)CC1CC2 FGUUNXDRMVKHCF-UHFFFAOYSA-N 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
HPXRVTGHNJAIIH-PTQBSOBMSA-N cyclohexanol Chemical class O[13CH]1CCCCC1 HPXRVTGHNJAIIH-PTQBSOBMSA-N 0.000 description 1
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000009434 installation Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1

JP2008215334A 2007-08-25 2008-08-25 低粘性の化学線硬化性基含有アロファネートの製造方法 Expired - Fee Related JP5591458B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE102007040239A DE102007040239A1 (de)	2007-08-25	2007-08-25	Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen
DE102007040239.4		2007-08-25

Publications (3)

Publication Number	Publication Date
JP2009062533A JP2009062533A (ja)	2009-03-26
JP2009062533A5 true JP2009062533A5 (2)	2011-10-06
JP5591458B2 JP5591458B2 (ja)	2014-09-17

Family

ID=39962036

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP2008215334A Expired - Fee Related JP5591458B2 (ja)	2007-08-25	2008-08-25	低粘性の化学線硬化性基含有アロファネートの製造方法

Country Status (12)

Country	Link
US (1)	US8106140B2 (2)
EP (1)	EP2031003B1 (2)
JP (1)	JP5591458B2 (2)
KR (2)	KR101546538B1 (2)
CN (1)	CN101372529B (2)
AT (1)	ATE538154T1 (2)
AU (1)	AU2008203813B2 (2)
BR (1)	BRPI0803887A2 (2)
CA (1)	CA2639103C (2)
DE (1)	DE102007040239A1 (2)
ES (1)	ES2377334T3 (2)
TW (1)	TWI421264B (2)

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DE102004048873A1 (de) *	2004-10-07	2006-04-13	Bayer Materialscience Ag	Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen
DE102009008569A1 (de)	2009-02-12	2010-08-19	Bayer Materialscience Ag	Verfahren zur Herstellung von besonders reaktiven und niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen und deren Verwendung zur Herstellung besonders kratzfester Beschichtungen
DE102009027395A1 (de) *	2009-07-01	2011-01-05	Evonik Degussa Gmbh	Reaktive Derivate auf Basis Dianhydrohexitol basierender Isocyanate
DE102009040333A1 (de) *	2009-09-05	2011-03-10	Bayer Materialscience Ag	Verfahren zur kontinuierlichen Herstellung von Allophanaten
US9023916B2 (en)	2010-09-30	2015-05-05	Voco Gmbh	Composite material comprising a monomer with a polyalicyclic structure element
US9079828B2 (en)	2010-09-30	2015-07-14	Voco Gmbh	Polymerizable compounds comprising a polyalicylic structure element
EP2436364B1 (de)	2010-09-30	2017-05-31	VOCO GmbH	Lackzusammensetzung umfassend ein Monomer mit einem polyalicyclischen Strukturelement
EP2436363B1 (de)	2010-09-30	2017-01-18	VOCO GmbH	Zusammensetzung umfassend ein Monomer mit einem polyalicyclischen Strukturelement zum Füllen und/oder Versiegeln eines Wurzelkanals
EP2436366B1 (de)	2010-09-30	2015-07-29	VOCO GmbH	Kompositmaterial umfassend ein Monomer mit einem polyalicyclischen Strukturelement als Versiegelungsmaterial
DE102011053030A1 (de)	2011-08-26	2013-02-28	Bayer Materialscience Aktiengesellschaft	Solarmodul und Verfahren zu seiner Herstellung
FR3003255B1 (fr)	2013-03-14	2015-10-02	Vencorex France	Allophanate polyacrylate
JP6281188B2 (ja) *	2013-03-28	2018-02-21	日油株式会社	ウレタン（メタ）アクリレート及びこれを含有する光硬化型樹脂組成物
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EP3424971A1 (de) *	2017-07-03	2019-01-09	HILTI Aktiengesellschaft	Urethanmethacrylat-verbindungen enthaltende reaktivharze, reaktivharzkomponenten sowie reaktivharz-systeme und deren verwendung
WO2019183315A1 (en) *	2018-03-23	2019-09-26	Covestro Llc	Polyol acid neutralization for low temperature uretdione curing
CN111234177B (zh) *	2020-03-20	2022-02-18	万华化学集团股份有限公司	一种大分子单体稳定剂及其制备方法
CN112300359A (zh) *	2020-05-27	2021-02-02	南京山维新材料科技有限公司	一种防雾化聚氨酯丙烯酸酯树脂及其制备方法
CN111718469A (zh) *	2020-06-17	2020-09-29	北京华腾新材料股份有限公司	水性聚氨酯及其制备方法、热封胶粘剂
EP4092064A1 (en)	2021-05-17	2022-11-23	Covestro Deutschland AG	Photo- and thermally curable resin useful for additive manufacturing
CN115820107B (zh) *	2022-12-19	2023-12-12	江苏睿浦树脂科技有限公司	一种uv光固化粉末涂料树脂及其制备方法

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DE19860041A1 (de)	1998-12-23	2000-06-29	Basf Ag	Durch Addition an Isocyanatgruppen als auch durch strahlungsinduzierte Addition an aktivierte C-C-Doppelbindungen härtbare Beschichtungsmittel
DE10205608A1 (de)	2002-02-11	2003-08-21	Degussa	Bei niedriger Temperatur härtbare feste uretdiongruppenhaltige Polyurethan-Pulverlackzusammensetzungen
DE10246512A1 (de)	2002-10-04	2004-04-15	Bayer Ag	Niedrigviskose strahlenhärtende und thermisch härtende Polyisocyanate
DE102004012903A1 (de)	2004-03-17	2005-10-06	Bayer Materialscience Ag	Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen
DE102004043540A1 (de) *	2004-09-09	2006-03-30	Bayer Materialscience Ag	Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen
DE102004043539A1 (de) *	2004-09-09	2006-03-30	Bayer Materialscience Ag	Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen
DE102004043537A1 (de) *	2004-09-09	2006-03-16	Bayer Materialscience Ag	Herstellung von neuen strahlenhärtenden Bindemitteln
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JP2006083273A (ja) *	2004-09-15	2006-03-30	Mitsui Chemicals Inc	アロファネート基含有（メタ）アクリレート樹脂組成物
DE102004048873A1 (de) *	2004-10-07	2006-04-13	Bayer Materialscience Ag	Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen
DE102005011231A1 (de)	2005-03-11	2006-09-14	Bayer Materialscience Ag	Spezielle Allophanate enthaltende, modifizierte Polyurethane
DE102006015709A1 (de) *	2006-04-04	2007-10-11	Bayer Materialscience Ag	Verfahren zur Herstellung von allophanathaltigen, durch aktinische Strahlung härtbaren Polyurethanprepolymeren mit erhöhter Beständigkeit

2007
- 2007-08-25 DE DE102007040239A patent/DE102007040239A1/de not_active Withdrawn
2008
- 2008-08-11 AU AU2008203813A patent/AU2008203813B2/en not_active Ceased
- 2008-08-16 AT AT08014570T patent/ATE538154T1/de active
- 2008-08-16 EP EP08014570A patent/EP2031003B1/de active Active
- 2008-08-16 ES ES08014570T patent/ES2377334T3/es active Active
- 2008-08-20 US US12/229,116 patent/US8106140B2/en active Active
- 2008-08-22 KR KR1020080082281A patent/KR101546538B1/ko active Active
- 2008-08-22 BR BRPI0803887-2A patent/BRPI0803887A2/pt not_active IP Right Cessation
- 2008-08-22 CA CA2639103A patent/CA2639103C/en not_active Expired - Fee Related
- 2008-08-22 TW TW097132008A patent/TWI421264B/zh active
- 2008-08-25 JP JP2008215334A patent/JP5591458B2/ja not_active Expired - Fee Related
- 2008-08-25 CN CN2008101463274A patent/CN101372529B/zh active Active
2015
- 2015-03-17 KR KR20150036611A patent/KR20150035964A/ko not_active Ceased

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