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 |
|---|---|---|---|---|---|---|
| 1 | 共聚物及其制备方法和作为粘结剂的用途 | CN200610087811.5 | 2006-05-26 | CN1869086A | 2006-11-29 | P·格勒克纳 |
| 本发明涉及基于特定丙烯酸酯单体的共聚物及其制备方法和在粘合剂和涂料中的应用。 | ||||||
| 2 | 一种α‑聚甲醛的生产方法 | CN201710106525.7 | 2017-02-27 | CN106832160A | 2017-06-13 | 范轩羽; 范希中; 张亚炜; 张恒铭; 刘轶; 王志强; 孙立丹; 谢永 |
| 本发明公开一种α‑聚甲醛的生产方法，其特征在于包括如下步骤：将浓度为50％～80％的甲醛加入低强度聚合机中边抽真空脱水边搅拌聚合，得初步聚合产物；将上述初步聚合产物通过挤出机传送至高强度捏合聚合机入口处，边传送边抽真空脱水；在初步聚合产物输入高强度捏合聚合机的同时，在高强度捏合聚合机入口处加入温度为50～90℃、浓度为50％～80％的甲醛，边搅拌边抽真空脱水，从高强度捏合聚合机出口处挤出，再粉碎烘干，即制得所述α‑聚甲醛。不需加入任何引发剂即可使甲醛多级聚合，制的无水的α‑聚甲醛，整个生产操作简单，生产成本低，可以广泛用于聚甲醛、聚甲氧基二甲醚等的生产中。 | ||||||
| 3 | 伯、仲或叔脂族C3-C8链烷醇胺或这些的混合物的亚硫酸盐的水溶液 | CN201410747809.0 | 2014-12-09 | CN104693481A | 2015-06-10 | R·伦克威特兹 |
| 本发明涉及伯、仲或叔脂族C3-C8链烷醇胺或这些的混合物的亚硫酸盐的水溶液，还涉及一种生产这些的方法以及这些作为氨基塑料树脂，尤其是用于生产表面涂料的蜜胺-甲醛缩合物用硬化剂的用途。 | ||||||
| 4 | 生产支化或交联聚缩醛树脂的方法 | CN98115978.8 | 1998-07-16 | CN1122054C | 2003-09-24 | 川口邦明; 山本薰; 芹泽肇 |
| 支化或交联聚缩醛树脂的吹塑性优越，具有抗冲击性如平面冲击强度和由其制备的模制品的内表面的光滑性，适于进行模塑，特别是吹塑。它可以通过在(D)阳离子聚合催化剂存在下本体聚合(A)三噁烷与(B)环醚和环缩甲醛及(C)多官能团缩水甘油醚化合物来生产，将通过混合环醚和/或环缩甲醛(B)与多官能团缩水甘油醚化合物(C)和阳离子聚合催化剂(D)所制得的混合物加入到三噁烷(A)中以进行聚合。 | ||||||
| 5 | 生产支化或交联聚缩醛树脂的方法 | CN98115978.8 | 1998-07-16 | CN1206018A | 1999-01-27 | 川口邦明; 山本薰; 芹泽肇 |
| 支化或交联聚缩醛树脂的吹塑性优越,具有抗冲击性如平面冲击强度和由其制备的模制品的内表面的光滑性,适于进行模塑,特别是吹塑。它可以通过在(D)阳离子聚合催化剂存在下本体聚合(A)三噁烷与(B)环醚和环缩甲醛及(C)多官能团缩水甘油醚化合物来生产,将通过混合环醚和/或环缩甲醛(B)与多官能团缩水甘油醚化合物(C)和阳离子聚合催化剂(D)所制得的混合物加入到三噁烷(A)中以进行聚合。 | ||||||
| 6 | Microparticles and their preparation consists of biodegradable polymers, containing fine particles ultrasound diagnostic agents and ultrasound contrast agents | JP3521891 | 1991-02-05 | JP3363912B2 | 2003-01-08 | レースリンク ゲオルク; アルベイラク セラル; ローテ マティアス; ズィーゲルト ヨアヒム |
| 7 | JPS6323979B2 - | JP6951280 | 1980-05-23 | JPS6323979B2 | 1988-05-18 | GYUI RABIIYU; BERUNAARU SHIRYON |
| 8 | 아크롤레인-방출 공중합체 및 이를 함유하는 함수 살생물 시스템 | KR1019970005069 | 1997-02-20 | KR100248453B1 | 2000-04-01 | 베를레페터; 크림머한스-페터; 트라게저마르틴; 쿤츠프란츠-루돌프 |
| 수성 시스템내의 단량체 아크롤레인의 방출 및 미생물에 대해 지속적인 효과를 나타내는 것을 특징하는 아크롤레인 및 하나 이상의 다가 알콜로부터 제조된 아크롤레인 중합체는 용해된 형태의 촉매를 포함하는 반응매질로 아크롤레인을 첨가하고 반응 매질의 온도가 50℃를 초과하지 않도록 하여 제조된다. 아크롤레인 중합체는 살생물제로서 수성 시스템에서 사용될 수 있다. | ||||||
| 9 | 탄소섬유를 포함하는 폴리케톤 수지 | KR1020100135893 | 2010-12-27 | KR1020120073960A | 2012-07-05 | 윤성균; 최수명; 김헌수 |
| PURPOSE: A polyketone resin including carbon fibers is provided to improve hardness, tensile strength, flexural strength, modulus, and specific gravity and prevent change in temperature and moisture absorption. CONSTITUTION: A polyketone resin including carbon fibers comprises 70-90 weight% of cord alternation polyketone polymer and 10-30 weight% of carbon fiber. The cord alternation polyketone polymer is composed of carbon monoxide and one or more ethylene based unsaturated hydrocarbon. The carbon fiber has a length of 100-900 microns and a diameter of 5-15 microns. The polyketone resin composition has a tensile strength of 1700-1900 kgf/cm^2 cm. | ||||||
| 10 | 수지 | KR1020127017870 | 2010-12-10 | KR1020120104595A | 2012-09-21 | 피체트,코린,스탠리; 새펠,콜린그라함 |
| 본 발명은 열경화성 수지, 특히 바이오수지와 같은 수지의 제조방법, 상기 방법에 사용하기 위한 성분들, 및 상기 방법으로부터 얻은 산물에 관한 것이다. 한면에서, 수지의 제조방법은: (1)휘발성 알데히드와 가교제를 반응시켜 얻은 알데히드-가교제를 제공하는 단계; (2) 비-휘발성 알데히드를 제공하는 단계; 및 (3) 알데히드-가교제 축합물과 비-휘발성 축합물을 결합시키고, 그것에 의해 수지를 형성하는 단계를 포함한다.
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| 11 | High-capacity nanoparticulate immobilization surface | EP07301514.1 | 2007-10-30 | EP2055727A1 | 2009-05-06 | Deshayes, Sophie; Henry, David |
Disclosed are articles comprising polyglutaraldehyde nanoparticulates modified substrates for use, for example, in binding biomolecules, and methods of making and using the modified substrates. |
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| 12 | MANUFACTURE OF POLYKETONES | EP00910380.5 | 2000-03-01 | EP1165649B1 | 2004-05-12 | GOLDFINGER, Marc, Bruce |
| Polyketones are manufactured by reacting an aromatic carboxylic acid with a bireactive aromatic compound, using as a catalyst a combination of a carboxylic acid anhydride and phosphoric acid, or equivalents thereof. The product polymers are useful as molding resins. | ||||||
| 13 | Aldehyde resins with reduced and stabilized free-formaldehyde content | EP95103604.5 | 1995-03-13 | EP0672693B1 | 2001-06-06 | Albrecht, Norman G.; Foran, Michael T. |
| A ketone/formaldehyde crosslinking additive having reduced and stabilized free-formaldehyde content and which are useful in starch based alkaline corrugating adhesive compositions are provided by a process wherein the ketone/aldehyde additives are treated with hydrogen peroxide and further with an urea compound. | ||||||
| 14 | Verwendung von Polykondensationsprodukten aus Acrolein und Formaldehyd als Biozide | EP82110923.8 | 1982-11-26 | EP0087509B1 | 1985-04-24 | Merk, Wolfgang, Dr. Dipl.-Chem.; Rink, Karl-Heinz, Dr. Dipl.-Chem. |
| 15 | Verfahren zur Herstellung von niedermolekularen Polyhydroxylverbindungen | EP78100656.4 | 1978-08-14 | EP0000910A1 | 1979-03-07 | Möhring, Edgar, Dr.; Müller, Hanns Peter, Dr.; Wagner, Kuno, Dr. |
Verfahren zur Herstellung von niedermolekularen Polyhydroxylverbindungen durch Selbstkondensation von Formaldehydhydrat in Gegenwart von löslichen oder unlöslichen Verbindungen von Metallen der zweiten bis vierten Hauptgruppe oder der zweiten bis achten Nebengruppe des periodischen Systems der Elemente als Katalysator sowie gegebenenfalls in Gegenwart von zur Endiolbildung befähigten Verbindungen als Cokatalysator und/oder von niedermolekularen und/oder höhermolekularen Polyhydroxylverbindungen, dadurch gekennzeichnet, dass der pH-Wert während der Kondensationsreaktion durch die Zugabe von 5 bis 200 Milliäquivalenten eines tertiären Amins, bezogen auf 1 Mol Formaldehyd, gesteuert wird. |
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| 16 | Method of manufacturing branched or crosslinked polyacetal resin | JP19126997 | 1997-07-16 | JP3771008B2 | 2006-04-26 | 薫 山本; 邦明 川口; 肇 芹澤 |
| 17 | Production of polyketone | JP2000602697 | 2000-03-01 | JP2002538248A | 2002-11-12 | ゴールドフインガー，マルク・ブルース |
| (57)【要約】 無水カルボン酸と燐酸またはそれらの相当物の組み合わせを触媒として用いて芳香族カルボン酸と二反応性芳香族化合物を反応させることでポリケトンを生じさせる。 生成物である重合体は成形用樹脂として用いるに有用である。 | ||||||
| 18 | Acrolein-releasing copolymers, their preparation, storage method of water-containing systems and materials for the biocide containing the same | JP3416697 | 1997-02-19 | JP3311629B2 | 2002-08-05 | クリマー ハンス−ペーター; クンツ フランツ−ルードルフ; ヴェルレ ペーター; トラゲザー マルティン |
| 19 | Production of branched or cross-linked polyacetal resin | JP19126997 | 1997-07-16 | JPH1135649A | 1999-02-09 | KAWAGUCHI KUNIAKI; YAMAMOTO KAORU; SERIZAWA HAJIME |
| PROBLEM TO BE SOLVED: To provide a method for producing a branched or crosslinked polyacetal resin excellent in both blow moldability and impact resistant characteristics such as a surface impact strength, further excellent in smoothness on the inner surface of a molding product and suitable for molding, especially for blow molding. SOLUTION: A mixture obtained by previously mixing (B) a cyclic ether and/or a cyclic formal and (C) a polyfunctional glycidyl ether compound and (D) a cationic polymerization catalyst is added to (A) trioxane, and the trioxane and the mixture are polymerized when producing the objective branched or cross-linked polyacetal resin by carrying out a bulk polymerization of (A) the trioxane, (B) the cyclic ether and/or the cyclic formal and (C) the polyfunctional glycidyl ether compound by using (D) the cationic polymerization catalyst. | ||||||
| 20 | Initiator for novel cationic polymerization | JP1749691 | 1991-02-08 | JPH04214704A | 1992-08-05 | OMAARU FUARUUKU |
| PURPOSE: To provide a novel cationic polymn. initiator being a compd. containing an onium cation and a non-nucleophilic metal complex anion and useful for forming a high mol.wt. polymer. CONSTITUTION: A novel cation polymn. initiator contains a compd. such as trimethyloxonium having constitution represented by formula I [wherein Y is a cation selected from a group consisting of oxonium, sulfonium, selenonium, iodonium, diazonium, pyrylium, carbenium and acylium, R is a group represented by formula II (wherein R 1 is H, halogen, alkyl or aryl) or a group represented by formula III, M is an element selected from group 3-15 elements, Z is 1-4 and a, b and n are an integer forming Z ≤ n and a×b=z]. This initiator is homogenously brought into contact with a cation polymerizable monomer such as styrene oxide to obtain a high mol.wt. polymer. COPYRIGHT: (C)1992,JPO | ||||||
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