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 | 含羟基和丙烯酸酯基支化聚合物的制备和用途 | CN201180023407.0 | 2011-05-09 | CN102892801B | 2016-01-13 | H-A·克罗克; 纪三郝; B·布鲁赫曼 |
本发明涉及含有羟基和丙烯酸酯基的支化聚合物,涉及其制备方法及其用途。 | ||||||
2 | 包含羟基和丙烯酸酯基的聚合物的制备及应用 | CN201080032252.2 | 2010-07-15 | CN102471430B | 2014-03-19 | H-A·克罗克; 纪三郝; B·布鲁赫曼; C·柔斯基 |
本发明涉及包含羟基和丙烯酸酯基的聚合物、涉及其制备方法并涉及其应用。 | ||||||
3 | 含羟基和丙烯酸酯基支化聚合物的制备和用途 | CN201180023407.0 | 2011-05-09 | CN102892801A | 2013-01-23 | H-A·克罗克; 纪三郝; B·布鲁赫曼 |
本发明涉及含有羟基和丙烯酸酯基的支化聚合物,涉及其制备方法及其用途。 | ||||||
4 | 开环吖内酯远螯聚合物 | CN200580033495.7 | 2005-09-19 | CN101035821A | 2007-09-12 | 杜安·D·范斯勒; 凯文·M·莱万多夫斯基; 巴布·N·加德丹 |
本发明描述了一种可固化组合物,包括迈克尔供体组分,多丙烯酰基组分,和1)具有反应性吖内酯官能团的烯键式不饱和单体,或者2)具有反应性开环吖内酯官能团的烯键式不饱和单体。同样描述了这些组分的反应产物即远螯聚合物。 | ||||||
5 | 芳香族烃甲醛树脂、改性芳香族烃甲醛树脂及环氧树脂、以及它们的制造方法 | CN201480035156.1 | 2014-06-16 | CN105339402B | 2017-07-28 | 东原豪; 大越笃 |
一种芳香族烃甲醛树脂,其为使下述式(1)表示的芳香族烃化合物(A)与甲醛(B)在酸性催化剂的存在下反应而得到的。(式(1)中,R表示碳数1~10的有机基团、l表示0~2的整数、m和n表示满足1≤m+n≤10、m≥0、n≥1的整数。) | ||||||
6 | 一种高性能减水剂及其制备方法 | CN201510917349.6 | 2015-12-10 | CN105542100A | 2016-05-04 | 丁小华; 李珊; 于新亚; 刘祥山; 杨扬; 袁柏; 黄旭日; 刘印才; 冯星望; 赵文昌; 王东; 白亚生 |
本发明公开了一种高性能减水剂,其分子结构式为:其中,R1、R2、R3、R4、R5、R6为H或碳数为1~4的烷基,a、b、c为重复单元的链节数,分子量为2000万~3000万。其与水泥具有良好的适应性。 | ||||||
7 | 芳香族烃甲醛树脂、改性芳香族烃甲醛树脂及环氧树脂、以及它们的制造方法 | CN201480035156.1 | 2014-06-16 | CN105339402A | 2016-02-17 | 东原豪; 大越笃 |
一种芳香族烃甲醛树脂,其为使下述式(1)表示的芳香族烃化合物(A)与甲醛(B)在酸性催化剂的存在下反应而得到的。(式(1)中,R表示碳数1~10的有机基团、l表示0~2的整数、m和n表示满足1≤m+n≤10、m≥0、n≥1的整数。) | ||||||
8 | 包含羟基和丙烯酸酯基的聚合物的制备及应用 | CN201080032252.2 | 2010-07-15 | CN102471430A | 2012-05-23 | H-A·克罗克; 纪三郝; B·布鲁赫曼; C·柔斯基 |
本发明涉及包含羟基和丙烯酸酯基的聚合物、涉及其制备方法并涉及其应用。 | ||||||
9 | 新颖的三烷和1,2,6-己三醇缩甲醛衍生物的聚缩醛共聚物 | CN90104385.0 | 1990-05-12 | CN1047074A | 1990-11-21 | 吉利A·布罗萨的; 安德鲁B·奥尔巴奇; 詹姆斯L·保尔 |
三烷与1,2,6-己三醇缩甲醛(HTF)或其酯衍生物进行阳离子催化共聚反应生成具有侧官能基团的缩醛共聚物。因此HTF或其酯衍生物可能含有选自羟基或酯基的官能基团,这些基团被保护,因此不与三烷发生共聚反应。然后,这些存留的基团可为后续的诸如嵌段共聚物的合成和/或使改性剂化学键合到缩醛共聚物主链上提供了官能反应点。 | ||||||
10 | HERSTELLUNG UND VERWENDUNG VON HYDROXYGRUPPEN UND ACRYLATGRUPPEN AUFWEISENDEN POLYMEREN | EP10730805.8 | 2010-07-15 | EP2454300A1 | 2012-05-23 | KLOK, Harm-Anton; JI, Sanhao; BRUCHMANN, Bernd; RÖSCH, Christine |
The present invention relates to polymers comprising hydroxy groups and acrylate groups, to a method for the production, and to the use thereof. | ||||||
11 | 芳香族炭化水素ホルムアルデヒド樹脂、変性芳香族炭化水素ホルムアルデヒド樹脂及びエポキシ樹脂、並びにそれらの製造方法 | JP2015522916 | 2014-06-16 | JPWO2014203867A1 | 2017-02-23 | 豪 東原; 篤 大越 |
下記式(1)で表される芳香族炭化水素化合物(A)とホルムアルデヒド(B)とを酸性触媒の存在下で反応させて得られる芳香族炭化水素ホルムアルデヒド樹脂。(式(1)中、Rは炭素数1〜10の有機基を示し、lは0〜2の整数、m及びnは1≦m+n≦10、m≧0、n≧1を満たす整数を示す。) | ||||||
12 | Production of acetal polymer and acetal copolymer | JP12397890 | 1990-05-14 | JPH0321618A | 1991-01-30 | JIERII EI BUROOSAADO; ANDORIYUU BII OOAABATSUKU; JIEEMUSU ERU POORU |
PURPOSE: To obtain an acetal polymer or copolymer having a specific structural formula and enhanced in chemical and physical characteristics by reacting trioxane and specific 1,2,6-hexanetriolformal (ester derivative). CONSTITUTION: Trioxane and 1,2,6-hexanetriolformal represented by formula I (X is a hydroxy radical or an ester radical) or an ester derivative thereof are subjected to cation polymerization to obtain an acetal copolymer represented by formula II (X is hydroxyl or ester and m and n are m+n=5-20,000 and n:m=1:5,000-1:1). When the acetal copolymer and a resin and/or a chemical group are reacted, a polyacetal polymer represented by formula III (X is a hydroxy radical or an ester radical) having chemical and/or physical characteristics having the resin and/or the chemical group is obtained. COPYRIGHT: (C)1991,JPO | ||||||
13 | JPS5036586A - | JP6805074 | 1974-06-14 | JPS5036586A | 1975-04-05 | |
14 | JPS4428509B1 - | JP3485366 | 1966-06-01 | JPS4428509B1 | 1969-11-22 | |
15 | HERSTELLUNG UND VERWENDUNG VON HYDROXYGRUPPEN UND ACRYLATGRUPPEN AUFWEISENDEN VERZWEIGTEN POLYMEREN | EP11717679.2 | 2011-05-09 | EP2569344B1 | 2014-07-23 | KLOK, Harm-Anton; JI, Sanhao; BRUCHMANN, Bernd |
16 | Novel polyacetal copolymers of trioxane and 1,2,6-hexanetriol formal derivatives | EP90305041.7 | 1990-05-10 | EP0397494A2 | 1990-11-14 | Broussard, Jerry A.; Paul, James L.; Auerbach, Andrew B. |
Cationic copolymerization of trioxane and 1,2,6-hexanetriol formal (HTF) or its ester derivatives yields acetal copolymers having pendant functional groups. The HTF formal or ester derivatives of HTF may therefore include functional groups selected from hydroxyl or ester moieties which are protected, and thus survive, the copolymerization with trioxane. These groups may then be present as functional reactive sites for the subsequent synthesis of block copolymers and/or to chemically bind modifiers to the acetal copolymer backbone, for example. |
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17 | Ring-opened azlactone-telechelic polymer | JP2007534647 | 2005-09-19 | JP2008514788A | 2008-05-08 | エヌ. ガッダム,バブ; ディー. ファンスラー,デュアン; エム. ルワンドウスキ,ケビン |
マイケル供与体成分、ポリアクリル成分、および1)反応性アズラクトン官能基を有するエチレン性不飽和モノマー、または2)反応性の開環アズラクトン官能基を有するエチレン性不飽和モノマーを含む硬化性組成物が記載される。 これらの成分の反応混合物であるテレケリックポリマーもまた記載される。 | ||||||
18 | The preparation of acetal polymer and acetal copolymer | JP12397890 | 1990-05-14 | JP2955326B2 | 1999-10-04 | JERII EI BUROOSAADO; ANDORYUU BII OOAABATSUKU; JEEMUSU ERU HOORU |
19 | JPS5124552B2 - | JP6805074 | 1974-06-14 | JPS5124552B2 | 1976-07-24 | |
20 | 폴리케톤의 제조방법 | KR1020100139302 | 2010-12-30 | KR1020120077367A | 2012-07-10 | 이부연; 최수명; 김헌수 |
PURPOSE: A manufacturing method of polyketone is provided to manufacture polyketone with improved catalyst activity and inherent viscosity by adding 3,5-di-tert-butyl-4-hydroxytoluene at polymerization. CONSTITUTION: A manufacturing method of polyketone comprises a step of copolymerization of an ethylenically unsaturated compound, and carbon monoxide in liquid medium under the presence of an organic metal complex. During the copolymerization, 3,5-di-tert-butyl-4-hydroxytoluene is added. The organic metal complex catalyst comprises: a transition metal compound of group 9, group 10, or group 11; a ligand having element from group 15; and acid anion having pKa of 4 or less. The liquid medium is mixed solvent consisting of 70-90 weight% of acetic acid, and 30-10 weight% of water. |