| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 41 | 炭水化物ポリアミン結合剤およびそれを用いて作製される材料 | JP2017158584 | 2017-08-21 | JP2017201043A | 2017-11-09 | チャールズ アップリー; カール ハンプソン; ゲルト ミューラー; ベネディクト パコレル |
| 【課題】炭水化物ポリアミン結合剤およびそれを用いて作製される材料を提供すること。 【解決手段】炭水化物反応物とポリアミンとの生成物を含む結合剤が開示される。この結合剤は、繊維など、緩く組み合わされた物体を強固に固めるのに有用である。炭水化物反応物およびポリアミンに接触した繊維を含む未硬化繊維生成物も開示される。結合剤組成物は、架橋ポリマーによって結合した繊維を含む繊維製品が得られるように、硬化することができる。炭水化物反応物およびポリアミンをベースにした結合剤で繊維を結合するための方法がさらに開示される。 【選択図】なし |
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| 42 | アミノプラスト架橋剤樹脂組成物、それらの調製方法及び使用方法 | JP2014536274 | 2012-10-21 | JP6122857B2 | 2017-04-26 | − タン ウィルソン リン、ロン; − ジョン ウー、クアン; 勝美 稲垣; ビリアーニ、ジョアン |
| 43 | ローラおよびローラ装置 | JP2011189311 | 2011-08-31 | JP5769013B2 | 2015-08-26 | 三宅 一徳 |
| 44 | アミノプラストを含む多孔質粒子 | JP2015503872 | 2013-04-04 | JP2015512463A | 2015-04-27 | フォン ベンテン レベッカ; シャーデ マティアス; シェル ギュンター; ユー ミラン |
| 本発明は、1〜500m2/gの比表面積及び5〜500μmの平均粒径を有する少なくとも1つのアミノプラストから製造されたアミノプラスト粒子に関する。本発明は、さらに、該アミノプラスト粒子を製造するための方法、アミノプラスト粒子を含む成形体、成形体の製造方法、アミノプラスト粒子の及び成形体の、例えばバッテリーにおけるプラスチック膜としての使用に関する。 | ||||||
| 45 | Materials carbohydrate binder and is fabricated using the same | JP2013508521 | 2011-05-07 | JP2013525586A | 2013-06-20 | チャールズ アップリー，; カール ハンプソン，; ゲルト ミューラー，; ベネディクト パコレル， |
| 炭水化物反応物と求核剤との生成物を含むポリマー結合剤を含む結合剤が開示される。 結合剤は、繊維など、緩く組み合わされた物体を強固に固めるのに有用である。 炭水化物反応物および求核剤に接触した繊維を含む繊維生成物も開示される。 結合剤組成物は、架橋ポリマーによって結合された繊維を含む繊維生成物が得られるように、硬化することができる。 炭水化物反応物およびポリアミンをベースにした結合剤で繊維を結合するための方法がさらに開示される。 | ||||||
| 46 | Color improvement of Dme- melamine resin | JP2000184478 | 2000-06-20 | JP4460726B2 | 2010-05-12 | ウィリアム・シー．・フロイド; バーナード・エフ．・ノース |
| 47 | Improvement of color of dme-melamine resin | JP2000184478 | 2000-06-20 | JP2001072732A | 2001-03-21 | FLOYD WILLIAM C; NORTH BERNARD F |
| PROBLEM TO BE SOLVED: To obtain a DME-melamine resin having a light color by reacting a specified amount of an amine derivative being at least either melamine or acetylenediurea with a specified amount of a dialkoxyethanal, and a specified amount of HCHO under basic conditions and further reacting the product under acidic conditions. SOLUTION: A mixture comprising 1 mol of an amine derivative being at least either melamine or acetylenediurea, about 1 to about 6 mol of a dialkoxyethanal, about 0.01 to about 2 mol of HCHO, and, optionally, about 0.01 to about 4 mol of a polyol is reacted under basic conditions of a pH of 8 or higher, and the product is further reacted under acidic conditions of a pH of 7 or lower. The alkoxyethanal is a compound of the formula, wherein R1 and R2 are each a 1-8C alkyl or they may be combined with each other to form a five- or six-membered ring acetal group. The polyol has at least two OH groups per molecule. A resin composition containing the reaction product is useful for coating for use in graphics, water-resistant coating, coating over the surface of a printed matter, or the like. | ||||||
| 48 | New polymeric acetal and derivatives of hydroxy carboxylic acids, and methods for producing them | JP51321198 | 1997-09-02 | JP2001503076A | 2001-03-06 | ヴァイネルト・フランク; クルーク・ペーター; ファルク・ウーヴェ |
| (57)【要約】 本発明は、以下の繰返し構造単位(I)（ここで、置換基及び数は本明細書に定義された意味を有する）を有するポリマー性アセタールに関する。 このポリマー性アセタールは、水溶性冷却潤滑剤の基本成分として適している。 | ||||||
| 49 | Coating composition for paper | JP15122294 | 1994-07-01 | JPH0813391A | 1996-01-16 | YOSHIDA YOSHIFUMI; HASEGAWA TOSHIYUKI; TANIKAWA AKIRA; KUMEI FUJIKO; KAWAMURA AKIRA |
| PURPOSE:To obtain a coating composition capable of imparting a paper with excellent printability and printing effect. CONSTITUTION:This coating composition contains (I) a pigment, (II) an aqueous binder and (III) a resin component consisting of a mixture or a reaction product of (A) a water-soluble resin produced by reacting (a) an alkylenediamine or a polyalkylene polyamine with (b) a urine compound and (c) a compound selected from aldehydes, epihalohydrins and alpha,gamma-dihalo-beta-hydrins and (B) an amide compound produced by reacting (x) an alpha,beta-unsaturated carboxylic acid compound with (y) a primary or secondary amino compound. The paper coated with the composition has excellent ink receptivity and water resistance. | ||||||
| 50 | JPH07502550A - | JP51131493 | 1992-12-24 | JPH07502550A | 1995-03-16 | |
| 51 | JPH0530788B2 - | JP25587084 | 1984-12-05 | JPH0530788B2 | 1993-05-10 | YOHAN PURANKU; AROISU AIKUNESUBERUGAA |
| 52 | Production of fine amino resin particle having narrow particle diameter distribution | JP5968589 | 1989-03-14 | JPH0320317A | 1991-01-29 | NAGAOKA MUNEO; HAYANO SABURO |
| PURPOSE: To obtain particles of an amino resin of a narrow particle diameter distribution without being overground by reacting an amino compound with an aldehyde in the presence of an acid catalyst in an aqueous medium and treating the slurry of the formed solid product by a combination of a plurality of grinding steps and classification steps. CONSTITUTION: A slurried solid polymer obtained by reacting an amino compound such as urea with an aldehyde in the presence of an acid catalyst in an aqueous solution is ground by a combination of a plurality of grinders and classifiers to obtain continuously amino resin particles (of a maximum particle diameter ≤40μm and a mean particle diameter of 5-15μm). A ball mill or an impact mill is used as the primary grinder, a vibrating screen or a hydrocyclone is used as the primary classifier, a pin mill is used as the secondary grinder, and a three-liquid classification cyclone is used as the secondary classifier. COPYRIGHT: (C)1991,JPO&Japio | ||||||
| 53 | Novel method for hardening amino plastic resin | JP14095889 | 1989-06-02 | JPH0229414A | 1990-01-31 | ROJIE GARIIGU; JIYATSUKU RARO; ANDORE BUINIYOO |
| PURPOSE: To improve the productivity and workability by using a hardening catalyst consisting of a strong acid salt of hexamethylene tetraamine and having a reactivity sufficiently different between in cooling and in heating in the hardening of amino plastic resin. CONSTITUTION: A strong acid salt of hexamethylene tetraamine is added as hardening catalyst to amino plastic resin (e.g.; urea formaldehyde resin) to harden the resin. Thus, the hardening speed of the resin can be regulated so that the hardening is not excessively quickly progressed, and the resin can be quickly hardened by heating and pressurizing within a press when a particle board is manufactured by this resin. The manufacture of the strong acid salt of hexamethylene tetraamine is attained by mixing a heated formaldehyde aqueous solution with an ammonia aqueous solution so that the mole ratio of formaldehyde/ammonia is 1.5, and adding a strong acid thereto so that pH is 1-7. COPYRIGHT: (C)1990,JPO | ||||||
| 54 | Steam turbine preservative and method of preserving steam turbine | JP29586688 | 1988-11-22 | JPH01163403A | 1989-06-27 | JIEEMUSU KURISUTOFUA BEROOZU |
| PURPOSE: To prevent corrosion by applying a mixture of an amine polymer and an organic solvent onto steam turbine components. CONSTITUTION: An amine polymer mixed with an organic solvent at a ratio of nearly 1:1 is applied onto steam turbine components. The amine polymer is preferably an amine polymer synthesized in the absence of halides. The organic solvent may be any suitable solvent provided that it is neither an aqueous solvent nor a halide solvent such as methylene chloride and the like. After the application, the solvent evaporates from the mixture within a short period of time and the amine polymer remains to protect the steam turbine components. As a consequence, corrosion can be prevented. COPYRIGHT: (C)1989,JPO | ||||||
| 55 | JPS6036233B2 - | JP7677882 | 1982-05-10 | JPS6036233B2 | 1985-08-19 | MAIKARU EI SHIRANO; ROBAATO DEIIN FUEZAASUTON |
| A crosslinking additive for imparting water resistance to starch-based corrugating adhesive compositions is prepared by reacting acetone and formaldehyde under aqueous alkaline conditions at 20 DEG -80 DEG C. in a molar ratio of 1 mole acetone to about 2 to 5.5 moles formaldehyde, adding to the reaction mixture at least an effective amount of dihydroxyethylene urea to scavenge the free formaldehyde in the mixture, and reacting until the amount of unreacted formaldehyde remaining is reduced to about 0.1-2%. The crosslinking additive thus obtained, which is low in free formaldehyde, may be added directly to a starch-based corrugating adhesive or may be first mixed with dimethylol dihydroxyethylene urea. | ||||||
| 56 | JPS5714708B2 - | JP5178874 | 1974-05-11 | JPS5714708B2 | 1982-03-26 | |
| 57 | Polyaddition product of ammonia and epoxy compound and its denaturing method | JP4576780 | 1980-04-09 | JPS55149318A | 1980-11-20 | FURITSUTSU ERUTOMAN KEMUPUTAA; EBERUHARUTO SHIYUTSUPU; HANSUUUUBUE SHIENKU; EERIHI GURUBINSU |
| 58 | JPS4948332B2 - | JP5916971 | 1971-08-05 | JPS4948332B2 | 1974-12-20 | |
| 59 | VERFAHREN ZUR HERSTELLUNG VON AMINOPLASTLÖSUNGEN | EP14178524.6 | 2014-07-25 | EP2835388B1 | 2016-12-28 | Finkenauer, Michael; Fuchs, Evelyn; Lunkwitz, Ralph; Reese, Oliver; Roschmann, Konrad; Schmidt, Michael; Reif, Martin; Weinkötz, Stephan |
| 60 | PROCESS FOR THE PREPARATION OF A PHENOL-FORMALDEHYDE RESIN HAVING A LOW AMOUNT OF FREE FORMALDEHYDE, A PHENOL-FORMALDEHYDE RESIN RESULTING FROM THIS PROCESS, AND THE USE OF THIS RESIN AS A BINDER FOR MINERAL WOOL INSULATION PRODUCTS | EP13719529.3 | 2013-04-26 | EP2841478A1 | 2015-03-04 | CASTRO-CABADO, Maria Mercedes; SANCHEZ PERUCHA, Alejandro; AZNAR ÉCIJA, Ana Isabel; CASADO DOMINGUEZ, Arturo Luis |
| The present invention relates to a process for reducing the content of free formaldehyde in a commercial phenol-formaldehyde resin, comprising the step of treating a phenol-formaldehyde resin with at least one phenol derivative or aniline derivative, wherein the pH of the resin is 7 or higher. The present invention further relates to a phenol-formaldehyde resin resulting from this process. The phenol-formaldehyde resin obtained by the process of the present invention may be used for the preparation of a binder composition for mineral wool products. | ||||||
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