| 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 | 制备缩合产物的低盐制剂的方法 | CN97114056.1 | 1997-06-26 | CN1173507A | 1998-02-18 | E·索勒马; W·扎格斯; H·特劳贝尔 |
| 制备基于以下化合物的缩合产物低盐制剂的方法,A)磺化芳族化合物,B)醛和/或酮和任选的C)一或多种选自非磺化的芳族化合物、尿素和/或尿素衍生物的化合物;其特征在于,将缩合后存在的无机酸在中和后可选地以其盐形式全部或部分从缩合产品中分离出来,直到无机盐含量少于10%(占制剂重量),产生非常适合作为鞣剂、分散剂和液化剂的制剂。 | ||||||
| 2 | カーボンナノチューブ分散剤 | JP2011543280 | 2010-11-25 | JP5716670B2 | 2015-05-13 | 飛田 将大; 齊藤 大悟; 畑中 辰也 |
| 3 | Phosphorus-containing curing agent and flame-retardant cured epoxy resin using the same | JP2000391241 | 2000-12-22 | JP3464783B2 | 2003-11-10 | 春山 王; 正▲悦▼ 謝 |
| 4 | CARBON NANO-TUBE COMPOSITION | EP10833241.2 | 2010-11-25 | EP2505260B1 | 2016-06-29 | HIDA Masahiro; SAITO Daigo; HATANAKA Tatsuya |
| Disclosed is a carbon nano-tube dispersant comprising a highly branched polymer having a repeating unit represented by, for example, formula (12) or (13), wherein the highly branched polymer is produced by the polycondensation of a triarylamine compound and an aldehyde compound and/or a ketone compound in the presence of an acid catalyst. The carbon nano-tube dispersant enables the dispersion of CNTs in a medium such as an organic solvent until the CNTs are so decomposed as to have an individual size. (In the formula, Z1 and Z2 independently represent a hydrogen atom, a phenyl group, a thienyl group, or the like.) | ||||||
| 5 | CARBON NANO-TUBE DISPERSANT | EP10833241.2 | 2010-11-25 | EP2505260A1 | 2012-10-03 | HIDA Masahiro; SAITO Daigo; HATANAKA Tatsuya |
Disclosed is a carbon nano-tube dispersant comprising a highly branched polymer having a repeating unit represented by, for example, formula (12) or (13), wherein the highly branched polymer is produced by the polycondensation of a triarylamine compound and an aldehyde compound and/or a ketone compound in the presence of an acid catalyst. The carbon nano-tube dispersant enables the dispersion of CNTs in a medium such as an organic solvent until the CNTs are so decomposed as to have an individual size.
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| 6 | 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: | ||||||
| 7 | Poly(ether ketone) polymers comprising cycloaliphatic units | US14653645 | 2013-12-19 | US09765176B2 | 2017-09-19 | Narmandakh Taylor; DeeDee Smith; David Blake Roller |
| A poly(ether ketone) polymer comprising recurring units derived from the reaction of at least one aromatic dihalo-compound comprising at least one —C(O)— group and at least one diol having a general formula HO-Dol-OH wherein Dol is an aliphatic group comprising from 4 to 20 carbon atoms which comprises at least one cycloaliphatic moiety. | ||||||
| 8 | CARBON NANO-TUBE DISPERSANT | US13511884 | 2010-11-25 | US20120268840A1 | 2012-10-25 | Masahiro Hida; Daigo Saito; Tatsuya Hatanaka |
| Disclosed is a carbon nano-tube dispersant comprising a highly branched polymer having a repeating unit represented by, for example, formula (12) or (13), wherein the highly branched polymer is produced by the polycondensation of a triarylamine compound and an aldehyde compound and/or a ketone compound in the presence of an acid catalyst. The carbon nano-tube dispersant enables the dispersion of CNTs in a medium such as an organic solvent until the CNTs are so decomposed as to have an individual size. (In the formula, Z1 and Z2 independently represent a hydrogen atom, a phenyl group, a thienyl group, or the like.) | ||||||
| 9 | Phosphorus-containing flame-retardant hardener, and epoxy resins cured by the same | US10618915 | 2003-07-14 | US06992151B2 | 2006-01-31 | Chun-Shan Wang; Jeng-Yueh Shieh |
| The present invention discloses an active-hydrogen-containing curing agent having a phosphorus group, and a flame retardant cured epoxy resin which can be prepared via an addition reaction between the active hydrogen and the epoxide group of an epoxy resin. The cured flame retardant epoxy resin is environmentally friendly and is suitable for printed circuit board and semiconductor encapsulation applications. The phosphorus group of the curing agent has a chemical structure as follows: wherein Ar is a substituted or un-substituted phenyl or phenoxy. | ||||||
| 10 | Phosphorus-containing flame-retardant hardener, and epoxy resins cured by the same | US10618915 | 2003-07-14 | US20040024255A1 | 2004-02-05 | Chun-Shan Wang; Jeng-Yueh Shieh |
| The present invention discloses an active-hydrogen-containing curing agent having a phosphorus group, and a flame retardant cured epoxy resin which can be prepared via an addition reaction between the active hydrogen and the epoxide group of an epoxy resin. The cured flame retardant epoxy resin is environmentally friendly and is suitable for printed circuit board and semiconductor encapsulation applications. The phosphorus group of the curing agent has a chemical structure as follows: 1 wherein Ar is a substituted or un-substituted phenyl or phenoxy. | ||||||
| 11 | Carboxylated naphthalene formaldehyde condensation polymers as dental plaque barriers | US172494 | 1980-07-25 | US4362712A | 1982-12-07 | Carl J. Buck |
| Polymers useful in compositions and methods for preventing the attachment of dental plaque to the surface of the teeth of mammals comprise alkali metal salts of certain carboxylated naphthalene formaldehyde polymers in a pharmaceutically acceptable vehicle and the periodic application thereof to teeth. | ||||||
| 12 | Process for the production of an indene phenol | US48733843 | 1943-05-17 | US2423415A | 1947-07-01 | SODAY FRANK J |
| 13 | POLY(ETHER KETONE) POLYMERS COMPRISING CYCLOALIPHATIC UNITS | EP13811538.1 | 2013-12-19 | EP2935401B1 | 2016-08-17 | TAYLOR, Narmandakh; SMITH, DeeDee; ROLLER, David Blake |
| A poly(ether ketone) polymer comprising recurring units derived from the reaction of at least one aromatic dihalo-compound comprising at least one —C(O)— group and at least one diol having a general formula HO-Dol-OH wherein Dol is an aliphatic group comprising from 4 to 20 carbon atoms which comprises at least one cycloaliphatic moiety. | ||||||
| 14 | POLY(ETHER KETONE) POLYMERS COMPRISING CYCLOALIPHATIC UNITS | EP13811538.1 | 2013-12-19 | EP2935401A2 | 2015-10-28 | TAYLOR, Narmandakh; SMITH, DeeDee; ROLLER, David Blake |
| A poly(ether ketone) polymer comprising recurring units derived from the reaction of at least one aromatic dihalo-compound comprising at least one —C(O)— group and at least one diol having a general formula HO-Dol-OH wherein Dol is an aliphatic group comprising from 4 to 20 carbon atoms which comprises at least one cycloaliphatic moiety. | ||||||
| 15 | CARBON NANO-TUBE DISPERSANT | EP10833241 | 2010-11-25 | EP2505260A4 | 2013-11-13 | HIDA MASAHIRO; SAITO DAIGO; HATANAKA TATSUYA |
| Disclosed is a carbon nano-tube dispersant comprising a highly branched polymer having a repeating unit represented by, for example, formula (12) or (13), wherein the highly branched polymer is produced by the polycondensation of a triarylamine compound and an aldehyde compound and/or a ketone compound in the presence of an acid catalyst. The carbon nano-tube dispersant enables the dispersion of CNTs in a medium such as an organic solvent until the CNTs are so decomposed as to have an individual size. (In the formula, Z1 and Z2 independently represent a hydrogen atom, a phenyl group, a thienyl group, or the like.) | ||||||
| 16 | Polymer for preparing resist underlayer film, resist underlayer film composition containing the polymer and method for manufacturing semiconductor device using the composition | US15207817 | 2016-07-12 | US09996007B2 | 2018-06-12 | Min Ho Jung; Yu Na Shim; Kyun Phyo Lee; Jin Su Ham; Soo Young Hwang |
| Provided are a polymer used for a manufacturing process of a semiconductor and a display, a resist underlayer film composition containing the polymer for a manufacturing process of a semiconductor and a display, and a method for manufacturing semiconductor device using the composition, and more specifically, the polymer of the present disclosure simultaneously has optimized etching selectivity, planarization characteristic, and excellent thermal resistance, such that the resist underlayer film composition containing the polymer is usable as a hard mask for a multilayer semiconductor lithography process. | ||||||
| 17 | Polymer for Preparing Resist Underlayer Film, Resist Underlayer Film Composition Containing the Polymer and Method for Manufacturing Semiconductor Device Using the Composition | US15207817 | 2016-07-12 | US20170015779A1 | 2017-01-19 | Min Ho Jung; Yu Na Shim; Kyun Phyo Lee; Jin Su Ham; Soo Young Hwang |
| Provided are a polymer used for a manufacturing process of a semiconductor and a display, a resist underlayer film composition containing the polymer for a manufacturing process of a semiconductor and a display, and a method for manufacturing semiconductor device using the composition, and more specifically, the polymer of the present disclosure simultaneously has optimized etching selectivity, planarization characteristic, and excellent thermal resistance, such that the resist underlayer film composition containing the polymer is usable as a hard mask for a multilayer semiconductor lithography process. | ||||||
| 18 | METHOD OF PRODUCING LAYER STRUCTURE, LAYER STRUCTURE, AND METHOD OF FORMING PATTERNS | US14740456 | 2015-06-16 | US20160126088A1 | 2016-05-05 | Min-Soo KIM; Hyun-Ji SONG; Sun-Hae KANG; Sung-Min KIM; Sung-Hwan KIM; Young-Min KIM; Yun-Jun KIM; Hea-Jung KIM; Youn-Hee NAM; Jae-Yeol BAEK; Byeri YOON; Yong-Woon YOON; Chung-Heon LEE; Seulgi JEONG; Yeon-Hee JO; Seung-Hee HONG; Sun-Min HWANG; Won-Jong HWANG; Songse YI; MyeongKoo KIM; Naery YU |
| A method of producing a layer structure includes forming a first organic layer by applying a first composition including an organic compound on a substrate having a plurality of patterns, applying a solvent on the first organic layer to remove a part of the first organic layer, and applying a second composition including an organic compound on a remaining part of the first organic layer and forming a second organic layer through a curing process. | ||||||
| 19 | Carbon nano-tube dispersant | US13511884 | 2010-11-25 | US09123893B2 | 2015-09-01 | Masahiro Hida; Daigo Saito; Tatsuya Hatanaka |
| Disclosed is a carbon nano-tube dispersant comprising a highly branched polymer having a repeating unit represented by, for example, formula (12) or (13), wherein the highly branched polymer is produced by the polycondensation of a triarylamine compound and an aldehyde compound and/or a ketone compound in the presence of an acid catalyst. The carbon nano-tube dispersant enables the dispersion of CNTs in a medium such as an organic solvent until the CNTs are so decomposed as to have an individual size. (In the formula, Z1 and Z2 independently represent a hydrogen atom, a phenyl group, a thienyl group, or the like.) | ||||||
| 20 | Polymeric species production | US679104 | 1991-04-02 | US5194563A | 1993-03-16 | Allan S. Hay |
| Linear aromatic polymeric species, particularly oligomers and polymers are produced under mild conditions in good yield by reacting an at least binuclear aromatic compound with an alkylidene bisphenol in the presence of a non C-alkylatable hydroxy substituted aromatic compound effective to stabilize a generated carbonium ion intermediate; the alkylidene bisphenol may be formed in situ from a ketone or aldehyde in the presence of a catalytic amount of a hydroxy substituted aromatic compound effective to generate a carbonium ion with the ketone or aldehyde; carrying out the reaction under reduced pressure, particularly high vacuum permits direct production of high polymers; the oligomers are useful in the manufacture of high molecular weight engineering or industrial plastics; the polymers may be used directly as such plastics. | ||||||
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