子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 81 | Polyaddition products having uretdione groups | JP2004518679 | 2003-07-03 | JP4533745B2 | 2010-09-01 | ハンス−ウルリッヒ・マイヤー−ヴェストヒュース; ハンス−ヨーゼフ・ラース; ペーター・トメツェク; ミヒャエル・グラール; ラインハルト・ハルパープ |
| 82 | Isocyanate containing uretdione groups | JP2004518680 | 2003-07-03 | JP4490813B2 | 2010-06-30 | ハンス−ヨーゼフ・ラース; フランク・リヒター; ユルゲン・ケッヒャー; ラインハルト・ハルパープ |
| 83 | Isocyanate containing uretdione groups | JP2004518680 | 2003-07-03 | JP2005531677A | 2005-10-20 | ハンス−ヨーゼフ・ラース; フランク・リヒター; ユルゲン・ケッヒャー; ラインハルト・ハルパープ |
| 本発明は、ウレトジオン基を有する新規の化合物、もっぱら第２級および／または第３級結合イソシアネート基を有する脂肪族および／または脂環式イソシアネートの二量化による該化合物の製造方法、およびもっぱら第２級および／または第３級結合イソシアネート基を有する脂肪族および／または脂環式ジイソシアネートから該方法によって得られるウレトジオンポリイソシアネートの、ポリウレタン樹脂の製造における出発成分として、特にウレトジオン粉体塗料架橋剤の製造のためのイソシアネート成分としての使用に関する。 | ||||||
| 84 | Polyaddition products having uretdione groups | JP2004518679 | 2003-07-03 | JP2005531676A | 2005-10-20 | ハンス−ウルリッヒ・マイヤー−ヴェストヒュース; ハンス−ヨーゼフ・ラース; ペーター・トメツェク; ミヒャエル・グラール; ラインハルト・ハルパープ |
| 本発明は、ウレトジオン基を有する新規の重付加化合物、その製造方法、およびポリウレタン樹脂の製造における出発成分としてのその使用に関する。 | ||||||
| 85 | JPS5442394B2 - | JP8201175 | 1975-07-04 | JPS5442394B2 | 1979-12-13 | |
| 86 | Katoseikitainohifukuhoho | JP8201175 | 1975-07-04 | JPS5130887A | 1976-03-16 | ARUBAATO SUTORAASERU |
| 87 | NON-AQUEOUS LIQUID COATING COMPOSITION | EP13709164.1 | 2013-03-04 | EP2822983B1 | 2018-11-21 | SCHERER, Taco; VAN BEELEN, Nicolaas Jacob; VAN DER PUTTEN, Antonius Josephus; VAN ADRICHEM, Arnoldus Adrianus Jozef Maria; BRUIN, David Elias; GAGLIARDO, Marcella |
| The invention relates to a non-aqueous liquid coating composition comprising a) a polyol, b) a polyisocyanate crosslinker c) one or more thiol-functional compounds, d) a metal-based curing catalyst for catalyzing the addition reaction of isocyanate groups and hydroxyl groups, e) a base having a pKa value of at least 7, and which base does not react with isocyanate groups in a way wherein the basicity is reduced, and f) one or more acid group-containing compounds, wherein the one or more thiol-functional compounds are present in an amount to provide a molar ratio of thiol groups over the metal atoms of the metal-based curing catalyst of 1 or higher, and wherein the base is present in a molar amount lower than the molar amount of thiol groups, and wherein the molar ratio of acid groups and base groups is 1:1 or higher. | ||||||
| 88 | POLY(AMIDE-IMIDE) COPOLYMER, METHOD OF MANUFACTURING THE SAME, POLY(AMIDE-IMIDE)COPOLYMER FILM, WINDOW FOR DISPLAY DEVICE, AND DISPLAY DEVICE | EP18156679.5 | 2018-02-14 | EP3366717A1 | 2018-08-29 | JEON, Hyunjeong; JEE, Sang Soo; JU, Kyeong-sik |
A poly(amide-imide) copolymer including an amide structural unit having an amide group in a polymer main chain and an imide structural unit having an imide group in a polymer main chain, wherein at least one imide structural unit includes a moiety cross-linked to an adjacent polymer main chain through an amide bond.
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| 89 | VERFAHREN ZUR HERSTELLUNG KOMPAKTER POLYURETHANE MIT VERBESSERTER HYDROLYSESTABILITÄT | EP16709060.4 | 2016-03-10 | EP3268405A1 | 2018-01-17 | KAMM, Andre; THOMAS, Hans-Josef |
| The present invention relates to a method for producing a polyurethane, comprising the reaction of a composition (Z1) at least comprising a compound (P1) that is reactive to isocyanates, and a composition (Z2), at least comprising a polyisocyanate, wherein the compound (P1) is or can be obtained through the reaction of at least one polyepoxide with a compound (V1) selected from the group consisting of polyetheramines and polyetherols. The present invention further relates to polyurethanes that are or can be obtained according to a method of this type, and the use of a polyurethane according to the invention for coating of piping, as a "field joint" or of underwater technology (subsea equipment) such as, for example, a "Christmas tree" for the off-shore field, as well as glass-syntactic polyurethane. | ||||||
| 90 | ORGANIC ELECTROLUMINESCENT ELEMENT | EP14861563 | 2014-11-12 | EP3070998A4 | 2017-08-09 | SHIKAUCHI YASUFUMI; NISHIMURA NAOYA; NAKAIE NAOKI |
| 91 | MICROBICIDAL POLYMERS AND METHODS OF USE THEREOF | EP14875281.9 | 2014-12-22 | EP3086648A1 | 2016-11-02 | NASSAR, Roger A.; YOUNG, Shirley; CHIATTELLO, Marion L.; OMAN, Mark |
| Provided herewith are microbicidal polymers comprising an alkylene oxide backbone comprising one or more alkyl and/or alkylene oxide primary branches, in which at least one of the alkyl and/or alkylene oxide primary branches is functionalized with a quaternary ammonium or fluorinated group, or at least two of the alkyl and/or alkylene oxide primary branches are functionalized with a quaternary ammonium and fluorinated group, the primary branches optionally contain one or more alkyl and/or alkylene oxide secondary branches that are functionalized with a quaternary ammonium or fluorinated group, compositions comprising the polymer and a carrier, and methods of using the same. | ||||||
| 92 | ORGANIC ELECTROLUMINESCENT ELEMENT | EP14861563.6 | 2014-11-12 | EP3070998A1 | 2016-09-21 | SHIKAUCHI Yasufumi; NISHIMURA Naoya; NAKAIE Naoki |
This organic electroluminescent element, which is provided with a light scattering film obtained by curing a composition for light scattering film formation containing, for example, a triazine ring-containing polymer represented by formula (AA), a crosslinking agent and a light-diffusing agent, has excellent current efficiency.
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| 93 | DISPERGIERADDITIVE AUF BASIS VON PHOSPHORSÄUREESTERDERIVATEN | EP12719935.4 | 2012-05-04 | EP2723484B1 | 2015-12-09 | GÖBELT, Bernd; NAGELSDIEK, René; OMEIS, Jürgen; PIESTERT, Frederik; PRITSCHINS, Wolfgang; MEZNARIK, Natasa; SCHRÖDER, Daniela; TIEGS, Werner |
| 94 | RESINES EPOXYDES BIOSOURCEES A REACTIVITE AMELIOREE | EP13710476.6 | 2013-02-18 | EP2817348A2 | 2014-12-31 | HABAS, Jean-Pierre; LAPINTE, Vincent; ULLOA HABAS, Amélia; GIANI, Olivia |
| The invention relates to biosourced epoxide resins including the product of the reaction of one or more biosourced epoxide lipid derivatives with at least one cross-linking agent in the presence of at least one co-reagent selected from among the glycidyl ether derivatives of biosourced polyols, or the product of the reaction of one or more glycidyl ether derivatives of biosourced polyols with at least one cross-linking agent. | ||||||
| 95 | DISPERGIERADDITIVE AUF BASIS VON PHOSPHORSÄUREESTERDERIVATEN | EP12719935.4 | 2012-05-04 | EP2723484A1 | 2014-04-30 | GÖBELT, Bernd; NAGELSDIEK, René; OMEIS, Jürgen; PIESTERT, Frederik; PRITSCHINS, Wolfgang; MEZNARIK, Natasa; SCHRÖDER, Daniela; TIEGS, Werner |
| The invention relates to phosphoric acid derivatives, which are present as urea urethanes and include a binder-receptive radical in addition to at least one phosphoric acid ester group. Said phosphoric acid derivatives are optimally qualified as wetting agents and dispersants. | ||||||
| 96 | BLOCKED ISOCYANATE CROSSLINKER SOLUTION | EP04813659.2 | 2004-12-10 | EP1697439B1 | 2010-11-03 | GARNER, Archie, W.; BRANDENBURGER, Larry, B. |
| A low viscosity blocked isocyanate solution can be made by reacting together a polymeric isocyanato compound and propylene glycol, or a polymeric primary or secondary amine and propyl carbonate. The resulting beta-hydroxypropyl urethane polymer can be combined with propylene glycol monomethyl ether as a reducing solvent to form a pourable high-solids solution with good flow properties at room temperature. The solution has lower viscosity than is obtained using ethylene glycol as a blocking agent or using several non-HAPS reducing solvents that are similar to propylene glycol monomethyl ether. The solution can readily be combined with electrodepositable paint ingredients to form a curable coating composition. | ||||||
| 97 | BLOCKED ISOCYANATE CROSSLINKER SOLUTION | EP04813659.2 | 2004-12-10 | EP1697439A1 | 2006-09-06 | GARNER, Archie, W.; BRANDENBURGER, Larry, B. |
| A low viscosity blocked isocyanate solution can be made by reacting together a polymeric isocyanato compound and propylene glycol, or a polymeric primary or secondary amine and propyl carbonate. The resulting beta-hydroxypropyl urethane polymer can be combined with propylene glycol monomethyl ether as a reducing solvent to form a pourable high-solids solution with good flow properties at room temperature. The solution has lower viscosity than is obtained using ethylene glycol as a blocking agent or using several non-HAPS reducing solvents that are similar to propylene glycol monomethyl ether. The solution can readily be combined with electrodepositable paint ingredients to form a curable coating composition. | ||||||
| 98 | METHOD OF COLLATING VOICE PATTERN IN VOICE RECOGNIZING APPARATUS | EP86902496.8 | 1986-04-16 | EP0266423A1 | 1988-05-11 | YASUDA, Seigo |
Pre-selection (B) is effected based upon data (A) on the head of a word of an unknown voice. If the unknown voice turns into voiceless condition (a), the pre-selection (B) is interrupted and a main selection (C) is effected. When the unknown voice is terminated, the result of main selection (C) is output. When the voiced condition (b) is established while the main selection (C) is being effected, on the other hand, the main selection (C) is interrupted and the pre-selection (B) is effected again. |
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| 99 | NON-AQUEOUS LIQUID COATING COMPOSITION | PCT/EP2013054235 | 2013-03-04 | WO2013131835A3 | 2014-04-03 | SCHERER TACO; VAN BEELEN NICOLAAS JACOB; VAN DER PUTTEN ANTONIUS JOSEPHUS; VAN ADRICHEM ARNOLDUS ADRIANUS JOZEF MARIA; BRUIN DAVID ELIAS; GAGLIARDO MARCELLA |
| The invention relates to a non-aqueous liquid coating composition comprising a) a polyol, b) a polyisocyanate crosslinker c) one or more thiol-functional compounds, d) a metal-based curing catalyst for catalyzing the addition reaction of isocyanate groups and hydroxyl groups, e) a base having a pKa value of at least 7, and which base does not react with isocyanate groups in a way wherein the basicity is reduced, and f) one or more acid group-containing compounds, wherein the one or more thiol-functional compounds are present in an amount to provide a molar ratio of thiol groups over the metal atoms of the metal-based curing catalyst of 1or higher, and wherein the base is present in a molar amount lower than the molar amount of thiol groups, and wherein the molar ratio of acid groups and base groups is 1:1 or higher. | ||||||
| 100 | BIOSOURCED EPOXIDE RESINS HAVING IMPROVED REACTIVITY | PCT/FR2013050331 | 2013-02-18 | WO2013124574A3 | 2014-07-03 | HABAS JEAN-PIERRE; LAPINTE VINCENT; ULLOA HABAS AMÉLIA; GIANI OLIVIA |
| The invention relates to biosourced epoxide resins including the product of the reaction of one or more biosourced epoxide lipid derivatives with at least one cross-linking agent in the presence of at least one co-reagent selected from among the glycidyl ether derivatives of biosourced polyols, or the product of the reaction of one or more glycidyl ether derivatives of biosourced polyols with at least one cross-linking agent. | ||||||
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