| 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 | 着色剂相容性涂料用合成增稠剂 | CN200580002055.5 | 2005-01-07 | CN1946815B | 2015-06-17 | 基里尔·N·巴基夫; 陆德凯; 黄迎捷; 阮清溪; 杰弗里·K·波利蒂斯 |
| 一种合成聚合物，其具有烷基或芳基化合物的疏水物嵌段的水溶性或水溶胀性聚合物骨架和端基和/或中间基团，所述疏水物包含可聚合环状单体或可聚合双键(或烯)基团或他们的衍生物。所述疏水物嵌段由两个或多个相同或不同疏水物单元组成。这些合成聚合物被用作流变改性剂，尤其是用于乳胶涂料中。 | ||||||
| 2 | 树状大分子及其制备方法 | CN201280029625.X | 2012-05-17 | CN103635515A | 2014-03-12 | I·A·汤姆林森; A·A·皮拉 |
| 本发明提供了新的树状大分子和制造它们的方法。所述树状大分子源自于式(III)的硝基烷基氧杂环丙烷化合物:其申R1、R2和R3如本发明中所述。 | ||||||
| 3 | 一种用于增粘剂的聚氧富烯基醇醚及其制备装置 | CN201610569082.0 | 2016-07-19 | CN106046341A | 2016-10-26 | 贺凤伟; 马晓和; 刘通; 胡展铭; 张玮; 王俊博; 代文双; 安长伟 |
| 本发明公开了一种用于增粘剂的聚氧富烯基醇醚，其化学结构式如下：R[X(C2H4O)n(C3H6)n‘(C4H8)n‘’H]m，式中：R—C5～C8醇，X—O，n、n’、n”—链长，m—总链长，n、n’、n”、m均为正整数；本发明还公开了所述用于增粘剂的聚氧富烯基醇醚的制备装置，包括第一原料液储液槽、第二原料液储液槽、第三原料液储液槽、液体混合器、反应釜和电控柜。该用于增粘剂的聚氧富烯基醇醚的增粘效果远高于原有的高分子聚醚，且泡沫远低于原有的高分子聚醚。该用于增粘剂的聚氧富烯基醇醚的制备装置能够远程控制反应釜的温度和压力，将反应釜的温控和压力进行远程控制可以很大程度降低事故的发生，现场不需要固定操作人员，安全性高。 | ||||||
| 4 | 树状大分子及其制备方法 | CN201280029625.X | 2012-05-17 | CN103635515B | 2015-11-25 | I·A·汤姆林森; A·A·皮拉 |
| 本发明提供了新的树状大分子和制造它们的方法。所述树状大分子源自于式(III)的硝基烷基氧杂环丙烷化合物:其申R1、R2和R3如本文中所述。 | ||||||
| 5 | 着色剂相容性涂料用合成增稠剂 | CN200580002055.5 | 2005-01-07 | CN1946815A | 2007-04-11 | 基里尔·N·巴基夫; 陆德凯; 黄迎捷; 阮清溪; 杰弗里·K·波利蒂斯 |
| 一种合成聚合物，其具有烷基或芳基化合物的疏水物嵌段的水溶性或水溶胀性聚合物骨架和端基和/或中间基团，所述疏水物包含可聚合环状单体或可聚合双键(或烯)基团或他们的衍生物。所述疏水物嵌段由两个或多个相同或不同疏水物单元组成。这些合成聚合物被用作流变改性剂，尤其是用于乳胶涂料中。 | ||||||
| 6 | 液态的固化性环氧树脂组合物和含有它的粘接剂 | CN201180043678.2 | 2011-09-13 | CN103097427A | 2013-05-08 | 龟谷直幸; 小野和男; 天池正登; 野村智哉 |
| 本发明的课题在于提供在含有环氧树脂的组合物中其贮藏稳定性、固化特性以及固化物的特性、特别是耐有机溶剂性优异的固化性环氧树脂组合物和由该组合物构成的粘接剂，由粘接强度优异的固化性环氧树脂组合物构成的粘接剂。本发明的固化性环氧树脂组合物是含有以下（A）和（B）的液态的固化性环氧树脂组合物。（A）环氧树脂或环氧·聚酯混合树脂，（B）含有以下（b1）和（b2）的包合配合物，（b1）式A（COOH）a（式中，A表示C1～C6的可具有取代基的链状烃基、可具有取代基的C3～C10的单环状烃基或可具有取代基的C6～C10的双环状烃基，a表示2或3）表示的羧酸化合物等，（b2）选自式（II）表示的化合物和1,8-二氮杂双环［5.4.0］十一碳烯-7中的至少1种。 | ||||||
| 7 | 聚砜聚醚嵌段共聚物，合成其的方法和由其制造的膜 | CN200580024377.X | 2005-07-21 | CN1989174A | 2007-06-27 | 托马斯·H·施瓦布 |
| 一种嵌段共聚物，包括：聚合物的至少一个嵌段，包括至少50摩尔％的重复单元(R1)，所述的重复单元(R1)由包括至少两个－S(＝O)2基团和至少三个芳环的至少一种芳香二卤代化合物和至少一种芳香二醇的缩聚反应形成(嵌段(A))，和聚合物的至少一个嵌段，包括至少50摩尔％的重复单元(R2)，所述的重复单元(R2)通过聚合至少一种环氧烷形成(嵌段(B))。合成所述的嵌段共聚物的方法。包括所述的嵌段共聚物的聚合物组合物。一种制品，特别是膜，包括所述的嵌段共聚物或所述的聚合物组合物。所述的膜在提纯液体或分离气体中的用途。 | ||||||
| 8 | 多元醇和聚合物分散多元醇的制造方法 | CN02128299.4 | 2002-07-16 | CN1257928C | 2006-05-31 | 丰田贤伯; 堀江彰雄; 和田浩志; 杉山佳世子; 赤木悦子 |
| 本发明提供一种聚亚氧烷基多元醇的制造方法，它是在催化剂的存在下，使环氧丙烷和环氧乙烷开环加聚在引发剂上，由此制造聚亚氧烷基多元醇，其特征在于，所述聚亚氧烷基多元醇用以下方法得到：在复合金属氰化物配位催化剂的存在下，使环氧丙烷开环加聚在引发剂上、形成亚氧丙基嵌段链，再使环氧乙烷和环氧丙烷无规地开环加聚在该嵌段链上，形成亚氧烷基无规链，接着变换催化剂，在碱金属催化剂的存在下，使环氧乙烷开环加聚，形成亚氧乙基嵌段链；所述聚亚氧烷基多元醇的羟基值为5-56mgKOH/g，引发剂残基的比例在25质量%以下，亚氧丙基嵌段链的比例为5～50质量%，亚氧乙基总含量为5～60质量%，且末端羟基中伯醇羟基的比率在60mol%以上。 | ||||||
| 9 | 多元醇和聚合物分散多元醇的制造方法 | CN02128299.4 | 2002-07-16 | CN1400231A | 2003-03-05 | 丰田贤伯; 堀江彰雄; 和田浩志; 杉山佳世子; 赤木悦子 |
| 本发明提供一种聚亚氧烷基多元醇的制造方法，它是在催化剂的存在下，使环氧丙烷和环氧乙烷开环加聚在引发剂上，由此制造聚亚氧烷基多元醇，其特征在于，所述聚亚氧烷基多元醇用以下方法得到：在复合金属氰化物配位催化剂的存在下，使环氧丙烷开环加聚在引发剂上、形成亚氧丙基嵌段链，再使环氧乙烷和环氧丙烷无规地开环加聚在该嵌段链上，形成亚氧烷基无规链，接着变换催化剂，在碱金属催化剂的存在下，使环氧乙烷开环加聚，形成亚氧乙基嵌段链；所述聚亚氧烷基多元醇的羟基值为5－56mgKOH/g，引发剂残基的比例在25质量％以下，亚氧丙基嵌段链的比例为5～50质量％，亚氧乙基总含量为5～60质量％，且末端羟基中伯醇羟基的比率在60mol％以上。 | ||||||
| 10 | TRANSPARENT FLEXIBLE HARD COATED FILM AND METHOD OF PRODUCING THE SAME | US15456891 | 2017-03-13 | US20170183533A1 | 2017-06-29 | Byeong-Soo BAE; Gwang-Mun CHOI; Ji-Hoon KO |
| The invention relates to a transparent flexible hard coated film and a method of producing the same, and more particularly, to a transparent flexible hard coated film including a scratch-resistant surface and a method of producing the same. | ||||||
| 11 | Additives to improve open-time and freeze-thaw characteristics of water-based paints and coatings | US15093355 | 2016-04-07 | US09644108B2 | 2017-05-09 | Charles F. Palmer, Jr.; Lester Arnold Haney; Calvin M. Wicker, Jr. |
| Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application. | ||||||
| 12 | PROCESS FOR ORGANOCATALYTIC RING-OPENING POLYMERIZATION | US14597618 | 2015-01-15 | US20150197599A1 | 2015-07-16 | Kerstin WISS; Sirus Zarbakhsh; Achim Loeffler; Peter Deglmann; Lothar Riebel; Michael Limbach; Ronald Lindner; Michael Ludwik Lejkowski; Julia Frauke Grosse-Willerich |
| The present invention relates to a process for organocatalytic ring-opening polymerization of at least one monomer M suitable for ring-opening polymerization, or of mixtures thereof, wherein, in a step (i), at least one N-heterocyclic compound is subjected in the presence of at least one Zerevitinov-active compound Z1 to a temperature of at least 80° C. for a period of at least 30 seconds and, in a step (ii), the monomer M is added and reacted. | ||||||
| 13 | Production method of poly (phenylene ether ether ketone) | US14128796 | 2012-06-22 | US08981035B2 | 2015-03-17 | Keiko Ichinose; Kohei Yamashita; Makito Yokoe; Koji Yamauchi |
| There is provided a production method of poly(phenylene ether ether ketone). The production method makes a cyclic poly(phenylene ether ether ketone) composition subjected to thermal ring-opening polymerization in the presence of a metal alkoxide and/or a metal phenoxide. The cyclic poly(phenylene ether ether ketone) composition includes 60% by weight or more of cyclic poly(phenylene ether ether ketone) and has a melting point of 270° C. or lower. | ||||||
| 14 | PROCESS FOR ORGANOCATALYTIC RING-OPENING POLYMERIZATION | US13850594 | 2013-03-26 | US20130253164A1 | 2013-09-26 | Kerstin Wiss; Sirus Zarbakhsh; Achim Loeffler; Peter Deglmann; Lothar Riebel; Michael Limbach; Ronald Lindner; Michael Ludwik Lejkowski; Julia Frauke Grosse |
| The present invention relates to a process for organocatalytic ring-opening polymerization of at least one monomer M suitable for ring-opening polymerization, or of mixtures thereof, wherein, in a step (i), at least one N-heterocyclic compound is subjected in the presence of at least one Zerevitinov-active compound Z1 to a temperature of at least 80° C. for a period of at least 30 seconds and, in a step (ii), the monomer M is added and reacted. | ||||||
| 15 | Novel polymers and uses thereof | US10587419 | 2005-01-20 | US20070154431A1 | 2007-07-05 | Naoshi Nagai; Masahiko Mitsuzuka; Kazuoki Nakai; Motoaki Isokawa; Shiro Nakatsuka; Daiki Taneichi; Shirou Honma; Toshimitsu Narutaki |
| Polymers having polyolefin segments as the side chain, with a structural unit represented by the following Formula (1): wherein A is an olefin polymer having a weight average molecular weight of 400 to 500,000; R is H, an alkyl group, or an aralkyl group; W and Z are each O, HN, or S; and x and y are each 0 or 1, with the proviso that at least one of them is 1. The polymer can be applied as an antistatic agent, a cosmetic additive, a releasing agent for toner, a pigment dispersant, a lubricant for vinyl chloride resins, a coating material, an emulsion composition and the like. | ||||||
| 16 | Colorant compatible synthetic thickener for paint | US11031187 | 2005-01-07 | US20050150418A1 | 2005-07-14 | Kirill Bakeev; De-Kai Loo; Angie Ma; Tuyen Nguyen; Jeffrey Politis |
| A synthetic polymer has a water-soluble or water-swellable polymer backbone and terminal groups and/or intermediate groups of blocks of hydrophobes of alkyl- or aryl compounds containing a polymerizable cyclic monomer or a polymerizable double bond (or alkene) group or derivatives thereof. The blocks of hydrophobes are composed of two or more units of the same or different hydrophobes. These synthetic polymers are used as rheology modifiers, especially in latex paints. | ||||||
| 17 | Wettable, flexible, oxygen permeable, substantially non-swellable contact lens containing polyoxyalkylene backbone units, and use thereof | US58496 | 1987-06-05 | US4780488A | 1988-10-25 | Kai C. Su; Frank F. Molock |
| Contact lenses which are optically clear, wettable, flexible, of high oxygen permeability and substantially non-swellable in the aqueous ocular environment of use, of a polymer containing polyoxyalkylene backbone units are disclosed, as well as the preparation thereof and methods of treating vision defects therewith. | ||||||
| 18 | Inorganic reinforcing phase dispersed and bonded to polymer matrix | US118326 | 1980-02-04 | US4251576A | 1981-02-17 | Peter G. Osborn; Desmond W. J. Osmond; Barrie J. Thorpe |
| Stable, fluid, mouldable and curable compositions are described from which may be fabricated composite materials, of improved mechanical properties, comprising an organic polymer matrix and a particulate inorganic reinforcing phase dispersed in and bonded to the matrix. The fluid compositions comprise (A) a polymerizable organic liquid having a viscosity not greater than 50 poise at the moulding temperature, (B) inorganic filler particles of defined size constituting at least 20% by volume, and optionally up to 90% by volume, of the total composition, and (C) a defined polymeric dispersant whereby the filler particles are stably dispersed in the polymerizable liquid. The generally low viscosity of the curable compositions enables them to be cast by simple techniques and polymerization of the component (A) yields the above-described composite materials. | ||||||
| 19 | Composite materials | US871406 | 1978-01-23 | US4221697A | 1980-09-09 | Peter G. Osborn; Desmond W. J. Osmond; Barrie J. Thorpe |
| Stable, fluid, moldable and curable compositions are described from which may be fabricated composite materials, of improved mechanical properties, comprising an organic polymer matrix and a particulate inorganic reinforcing phase dispersed in and bonded to the matrix. The fluid compositions comprise (A) a polymerizable organic liquid having a viscosity not greater than 50 poise at the molding temperature, (B) inorganic filler particles of defined size constituting at least 20% by volume, and optionally up to 90% by volume, of the total composition, and (C) a defined polymeric dispersant whereby the filler particles are stably dispersed in the polymerizable liquid. The generally low viscosity of the curable compositions enables them to be cast by simple techniques and polymerization of the component (A) yields the above-described composite materials. | ||||||
| 20 | Additives to improve open-time and freeze-thaw characteristics of water-based paints and coatings | US15419433 | 2017-01-30 | US09963610B2 | 2018-05-08 | Charles F. Palmer, Jr.; Lester Arnold Haney; Calvin M. Wicker, Jr. |
| Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application. | ||||||
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