序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
1 化合物多胺粘合剂及用其制备的材料 CN201510524023.7 2011-05-07 CN105176460A 2015-12-23 C·爱普雷; C·哈姆普森; G·穆勒; B·帕克雷尔
披露了一种包含化合物反应物与多胺的产物的粘合剂。该粘合剂适用于固结松散组装的物质,例如纤维。披露了包含与碳水化合物反应物及多胺接触的纤维的未固化纤维产品。粘合剂组合物可固化以产生包含由交联聚合物粘合的纤维的纤维产品。进一步披露了用于以基于碳水化合物反应物及多胺的粘合剂粘合纤维的方法。
2 改进的聚(芳基醚)类以及生产它们的方法 CN200880102929.8 2008-08-08 CN101809063B 2013-08-14 昌塔尔·路易斯; 萨切特·斯里尼瓦桑; 威廉·甘迪
具有优异的熔体稳定性、较低的凝胶含量以及较低色度的改进聚(芳基醚)类以及用于生产它们的一种新方法。
3 改进的聚(芳基醚)类以及生产它们的方法 CN200880102929.8 2008-08-08 CN101809063A 2010-08-18 昌塔尔·路易斯; 萨切特·斯里尼瓦桑; 威廉·甘迪
具有优异的熔体稳定性、较低的凝胶含量以及较低色度的改进聚(芳基醚)类以及用于生产它们的一种新方法。
4 含磷阻燃酚树脂及以其为原料制备的阻燃环树脂固化 CN201310255770.6 2013-06-25 CN103382242B 2015-06-24 沈琦; 李旭锋; 赵冬
含磷酚树脂,属新型化合物技术领域,是用苯酚类化合物、双酚类化合物与甲醛合成酚醛树脂,然后将酚醛树脂与芳香性磷酸酯混合进行缩聚反应获得,具有合适的反应性、宽广的压合加工区间、高玻璃化转变温度、优异的耐热性、低吸性及良好的电气性能,可作为环树脂的固化剂,通过该化合物的酚羟基与环氧树脂的环氧基反应,可形成对环境友好的无卤阻燃环氧树脂固化物,可用于集成电路板以及半导体的封装材料使用。
5 化合物粘合剂及用其制备的材料 CN201180022851.0 2011-05-07 CN103025777A 2013-04-03 C·爱普雷; C·哈姆普森; G·穆勒; B·帕克雷尔
发明披露了一种包括聚合物粘合剂的粘合剂,该聚合物粘合剂包含化合物反应物与亲核试剂的产物的粘合剂。该粘合剂适用于固结松散组装的物质,例如纤维。还披露了包含与碳水化合物反应物及亲核试剂接触的纤维的纤维产品。粘合剂组合物可固化以产生包含由交联聚合物粘合的纤维的纤维产品。进一步披露了用于以基于碳水化合物反应物及亲核试剂的粘合剂粘合纤维的方法。
6 冷固性模制料粘结剂及其应用 CN87107941 1987-11-20 CN87107941A 1988-08-10 马克·托布斯; 阿莱克桑达·吴本维克; 弗朗茨·耶曼; 格拉德·拉迪格尔迪; 威利·塞斯; 迪克·林格曼
为制得浇铸模制件,可先用粒状基础模制料(砂),反应性酚()溶液和强酸(硫酸和/或磺酸)制成模制料混合物,然后再导入气态缩醛(二甲基缩甲醛)以使其固化。缩醛在酸作用下水解并释放出甲醛与醛反应性酚反应而交联成热固性塑料(酚醛树脂)。酸同时作为交联催化剂。“醛反应性酚”优选为间苯二酚或其产物如间苯二酚沥青或醛不足量时形成如以间苯二酚-甲醛或苯酚-间苯二酚-甲醛或间苯二酚-蜜胺-甲醛为基础形成的预缩合物。
7 化合物粘合剂及用其制备的材料 CN201180022851.0 2011-05-07 CN103025777B 2016-01-20 C·爱普雷; C·哈姆普森; G·穆勒; B·帕克雷尔
披露了一种包括聚合物粘合剂的粘合剂,该聚合物粘合剂包含化合物反应物与亲核试剂的产物的粘合剂。该粘合剂适用于固结松散组装的物质,例如纤维。还披露了包含与碳水化合物反应物及亲核试剂接触的纤维的纤维产品。粘合剂组合物可固化以产生包含由交联聚合物粘合的纤维的纤维产品。进一步披露了用于以基于碳水化合物反应物及亲核试剂的粘合剂粘合纤维的方法。
8 化合物多胺粘合剂及用其制备的材料 CN201180022853.X 2011-05-07 CN103025778B 2015-09-30 C·爱普雷; C·哈姆普森; G·穆勒; B·帕克雷尔
披露了一种包含化合物反应物与多胺的产物的粘合剂。该粘合剂适用于固结松散组装的物质,例如纤维。披露了包含与碳水化合物反应物及多胺接触的纤维的未固化纤维产品。粘合剂组合物可固化以产生包含由交联聚合物粘合的纤维的纤维产品。进一步披露了用于以基于碳水化合物反应物及多胺的粘合剂粘合纤维的方法。
9 可交联聚缩酯、其制造方法和用途 CN201380070291.5 2013-11-12 CN104937007A 2015-09-23 B·D·马伦; E·J·莫利托
发明公开了通过将多元醇用至少2个当量的羧酸酯化以产生中间体聚酮基羧酸酯而获得的可交联聚缩酮酯。然后中间体聚酮基羧酸酯被缩酮化以产生可交联聚缩酮酯,然后所述可交联聚缩酮酯可用于组合物中或被交联。
10 含磷阻燃酚树脂及以其为原料制备的阻燃环树脂固化 CN201310255770.6 2013-06-25 CN103382242A 2013-11-06 沈琦; 李旭锋; 赵冬
含磷酚树脂,属新型化合物技术领域,是用苯酚类化合物、双酚类化合物与甲醛合成酚醛树脂,然后将酚醛树脂与芳香性磷酸酯混合进行缩聚反应获得,具有合适的反应性、宽广的压合加工区间、高玻璃化转变温度、优异的耐热性、低吸性及良好的电气性能,可作为环树脂的固化剂,通过该化合物的酚羟基与环氧树脂的环氧基反应,可形成对环境友好的无卤阻燃环氧树脂固化物,可用于集成电路板以及半导体的封装材料使用。
11 化合物多胺粘合剂及用其制备的材料 CN201180022853.X 2011-05-07 CN103025778A 2013-04-03 C·爱普雷; C·哈姆普森; G·穆勒; B·帕克雷尔
披露了一种包含化合物反应物与多胺的产物的粘合剂。该粘合剂适用于固结松散组装的物质,例如纤维。披露了包含与碳水化合物反应物及多胺接触的纤维的未固化纤维产品。粘合剂组合物可固化以产生包含由交联聚合物粘合的纤维的纤维产品。进一步披露了用于以基于碳水化合物反应物及多胺的粘合剂粘合纤维的方法。
12 냉간경화의 성형 결합제 및 이를 이용한 성형물의 제조방법 KR1019880700844 1987-11-07 KR1019960004414B1 1996-04-03 마렉토르부스; 알렉산더부예빅; 프란쯔예르만; 게라르트라데구르디; 빌리자이스; 디르크링에만
내용 없음.
13 강화 플라스틱용 레조르시놀-변성 페놀계 수지 결합제 KR1019900001455 1990-02-07 KR1019930004363B1 1993-05-26 티오도르하비다일레이제이알
내용 없음.
14 CARBOHYDRATE POLYAMINE BINDERS AND MATERIALS MADE THEREWITH US15911411 2018-03-05 US20180265633A1 2018-09-20 Charles Fitch APPLEY; Carl HAMPSON; Gert R. MUELLER; Benedicte PACOREL
A binder comprising the products of a carbohydrate reactant and polyamine is disclosed. The binder is useful for consolidating loosely assembled matter, such as fibers. Uncured fibrous products comprising fibers in contact with a carbohydrate reactant and a polyamine are also disclosed. The binder composition may be cured to yield a fibrous product comprising fibers bound by a cross-linked polymer. Further disclosed are methods for binding fibers with the carbohydrate reactant and polyamine based binder.
15 Blocked 1,8-diazabicyclo[5.4.0]undec-7-ene bicarbonate catalyst for aerospace sealants US14964785 2015-12-10 US09988487B2 2018-06-05 Hongying Zhou; Juexiao Cai; Renhe Lin
Compositions comprising sulfur-containing prepolymers such as polythioether prepolymers, polyepoxides, and a blocked 1,8-diazabicyclo[5.4.0]undec-7-ene bicarbonate catalyst useful as aerospace sealants are disclosed. The compositions exhibit extended working time and the curing rate can be tailored for specific applications.
16 Polymer, organic layer composition, organic layer, and method of forming patterns US15172351 2016-06-03 US09971243B2 2018-05-15 Yu-Shin Park; Tae-Ho Kim; Yoo-Jeong Choi; Sun-Hae Kang; Hyo-Young Kwon; Sang-Kyun Kim; Young-Min Kim; Youn-Hee Nam; Hyun-Ji Song; Byeri Yoon; Dong-Geun Lee; Seulgi Jeong
A polymer includes a structural unit represented by Chemical Formula 1 and an organic layer composition including the same. wherein in Chemical Formula 1, A is a carbon cyclic group including at least one hetero atom, B is one of groups in Group 1, where Ar1 to Ar4, R11 to R14, L and m are as defined in the specification and * is a linking point. When the carbon cyclic group includes at least two hetero atoms when the carbon cyclic group includes a pentagon cyclic moiety and the pentagon cyclic moiety includes a nitrogen atom (N) as a hetero atom, and the at least two hetero atoms are the same or different:
17 BLOCKED 1,8-DIAZABICYCLO[5.4.0]UNDEC-7-ENE BICARBONATE CATALYST FOR AEROSPACE SEALANTS US14964785 2015-12-10 US20170166689A1 2017-06-15 Hongying Zhou; JUEXIAO CAI; RENHE LIN
Compositions comprising sulfur-containing prepolymers such as polythioether prepolymers, polyepoxides, and a blocked 1,8-diazabicyclo[5.4.0]undec-7-ene bicarbonate catalyst useful as aerospace sealants are disclosed. The compositions exhibit extended working time and the curing rate can be tailored for specific applications.
18 Photoalignment of materials including liquid crystals US13786904 2013-03-06 US09441163B2 2016-09-13 Timothy M. Swager; Jason R. Cox
Embodiments described herein relate to compositions, devices, and methods for the alignment of certain materials including liquid crystals. In some cases, a photoresponsive material include a moiety capable of undergoing a di-pi-methane rearrangement. Methods described herein may provide chemically and/or thermally stable alignment materials for use in a various technologies, including transistors, luminescent devices, and liquid crystal devices.
19 Phosphor-containing phenol formaldehyde resin and flame-retardant epoxy resin hardener containing thereof US14312703 2014-06-24 US09359469B2 2016-06-07 Qi Shen; Xu-Feng Li; Dong Zhao
The introduction of environmentally-friendly organic phosphorus group can not only maintain the original excellent properties of epoxy resins, but also meet the high flame-retarding requirements, and have the ability to improve the vitrification temperature (Tg), heat resistance and other characteristics of the material so that the curing system can be successfully applied to the electronic materials field which are light, thin, small and precise, the present disclosure provides a flame-retarding phosphor-containing phenol-formaldehyde novolac and the preparation method thereof, the use of the compound to react with the epoxy group of an epoxy resin to obtain an environmentally-friendly and high performing halogen-free cured flame retarding epoxy resin, and the compound can also be used for curing epoxy resins and gives a high flame-retarding effect.
20 LIQUID HIGH SOLIDS BINDER COMPOSITION US14116048 2012-05-06 US20140186635A1 2014-07-03 Gert Mueller
The invention described herein pertains to formaldehyde free, thermosetting liquid high solids binder compositions having rapid cure times on thermal curing and slow cure times at ambient temperatures so that the uncured binder compositions and products which comprise the uncured binder compositions have improved shelf lives.
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