序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
141 Preparation of aromatic polyester polyols from dimethyl terephthalate process residue and tall oil fatty acid JP7856390 1990-03-27 JPH0813875B2 1996-02-14 ジョン・エム・トロウェル; スコット・エフ・ランジ
142 Process for thermoforming polyisocyanurate foam JP15702192 1992-06-16 JPH07188441A 1995-07-25 KENESU PII KURATSUPAA; UEIN II RAFURIN
PURPOSE: To obtain a polymer foam material suitable for use in the field of the interior finishing by foaming and thermoforming a foam-forming mixture using an organic polyisocyanate and a polyester diol at a specific equivalent ratio and added with a blowing agent and a catalyst. CONSTITUTION: Polyisocyanurate foams are thermoformed by the steps of (a) preparing a foam-forming mixture containing an organic polyisocyanate, a polyester polyol, or a polyester polyol and a polyol of at least one other OH group-containing compound, a blowing agent and a catalyst at an equivalent ratio of isocyanate groups to hydroxy groups of at least 1.2:1; (b) foaming the mixture (a) for preparing a polyisocyanurate foam; and (c) thermoforming this polyisocyanurate foam to a desired shape. COPYRIGHT: (C)1995,JPO
143 Preparation of polyurethane foam JP24103293 1993-09-28 JPH06206962A 1994-07-26 URURITSUHI RIIMAN; HARUTOBUITSUHI GURANMESU; DEIRUKU BUEEGENAA; MANUERU KAIZAA
PURPOSE: To obtain the subject foams useful as composite films, etc., having superior heat aging resistance by reacting a specified reactive mixture, a blowing agent and a specified salt of α,β-unsatd. carboxylic acid in specific amounts. CONSTITUTION: A reactive mixture consisting of (A) a poly-isocyanate component and (B) a polyol component free of salt group is reacted in the presence of (C) at least one blowing agent and (D) a salt of ester-functional α,β-unsatd. carboxylic acid comprising (i) alcohol selected from the groups consisting of monohydric ether-functional alcohols having a molecular weight of a range of 76-4000, polyhydric optionally ether-functional alcohols having a molecular weight of a range of 62-8000, and their mixtures, and (ii) a salt of a reactive product of α,β-unsatd. carboxylic acid (intermolecular anhydride), whose salt has at least one alkali metal carboxylate group per one molecule on a statistical average and at most 0.5 alcoholic hydroxyl group in an amount of 0.01-100 wt.% based on the component B, to obtain objective foams. COPYRIGHT: (C)1994,JPO
144 JPH05505850A - JP50083892 1991-10-28 JPH05505850A 1993-08-26
145 Thermosetting polyurethane structural adhesive composition and preparation thereof JP9383490 1990-04-09 JPH0372587A 1991-03-27 CHIYAARUZU KODEI; TERENSU HAATOMAN
PURPOSE: To obtain a thermosetting polyurethane structural adhesive compsn. which possesses good green strength, structural adhesion, and heat resistance and can be adhered to various substrates by dispersing an amine-terminated polyamide resin in a polyurethane base resin in a specific temp. range and heating the resultant composite in a specific temp. range. CONSTITUTION: An amine-terminated polyamide resin is dispersed in a polyurethane base resin at a temp. of about 25 to 200°C to form a composite which is then heated to about 50 to 250°C to prepare the thermosetting polyurethane structural adhesive compsn. In this case, the polyurethane base resin is a resin that has an m.p. at least about 5°C, most pref. about 40°C, below the m.p. of the amine-terminated solid polyamide resin. 4,4'-Diphenylmethane diisocyanate is a polyisocyanate compd. preferable in the preparation of the polyurethane base resin. The above adhesive compsn. has a fast-setting property and superior green strength, structural adhesion, and heat resistance to conventional adhesive compsns. and can be adhered to a wide variety of substrates and hence can be applied to a variety of fields. COPYRIGHT: (C)1991,JPO
146 Polyisocyanurate foam JP10856090 1990-04-24 JPH0320319A 1991-01-29 SUKOTSUTO SHII SUNAIDAA; MAIKERU II RONDORIGAN; KENESU JII TOROOTO
PURPOSE: To obtain polyisocyanurate foam excellent in heat insulating characteristics, dimensional stability, heat resistance and compression strength by reacting a terminal NCO group-containing a prepolymer and a specific polyol component in the presence of a foaming agent and a catalyst to produce a reaction product. CONSTITUTION: High heat insulating polyisocyanurate foam is obtained by reacting a prepolymer (A) having an NCO group at its terminal (reaction product of org. polyisocyanurate and an org. compd. having at least two active hydrogen atoms, for example, toluendiisocyanate, diphenylmethanediisocyanate), aromatic polyester polyol (free glycol component content: 7 wt.% or less), a foaming agent (C) and a catalyst (D). COPYRIGHT: (C)1991,JPO
147 Humidity curable hot-melt polyurethane adhesive composition JP10994090 1990-04-25 JPH036281A 1991-01-11 HAINTSU GERUHARUTO GIRUHI; BUARUTAA RAATO; KAARUSHIYUTEN ZAITSU
PURPOSE: To drastically increase a curing speed as compared with that of a non-foamed adhesive compsn. by foaming adhesive compsn., by foaming a humidity curable hot-melt polyurethane adhesive compsn. containing a specific isocyanate terminal polyurethane prepolymer. CONSTITUTION: A humidity curable hot-melt polyurethane adhesive compsn. contains an isocyanate terminal polyurethane prepolymer having an m.p. of 40-60°C or a phase transition point higher than room temp. and is based on a polyester or poyether. This compsn. is produced as foam by introducing an inert gas into the molten compsn. under pressure and releasing the pressure of the obtained compsn. to the circumferential pressure. The obtained foam is cured at a curing speed at least 10 times, pref., at least 100 times the curing speed of the non-foamed compsn. A surfactant and a nucleating agent may be compounded with the compd. COPYRIGHT: (C)1991,JPO
148 Novel polyol blend and polyisocyanurate foam manufactured therefrom JP3314186 1986-02-19 JPS61195108A 1986-08-29 RICHIYAADO BII TAIDOZUUERU; NEIRU EICHI NODERUMAN; BARII EI FUIRITSUPUSU
149 JPS5835607B2 - JP3469480 1980-03-21 JPS5835607B2 1983-08-03 KURODA AKIRA; NAKAMURA TSUTOMU; OONISHI MASATOSHI
150 Polymer foam manufacture JP13820480 1980-10-02 JPS5659830A 1981-05-23 DEBITSUDO TOOMASU DEGIYUISETSU; RICHIYAADO ANSONII KORAKOUSUKI
151 イソシアネート/シロキサンポリエーテル組成物 JP2016520343 2014-05-26 JP2016526585A 2016-09-05 クリスチアン エイルブラヒト; カルステン シーレル; マルティン グロス
本発明は、ウレタン結合を介して有機基、好ましくは1個以上のイソシアネート基及び/又はポリウレタン結合を有する有機基に結合される少なくとも1個のポリエーテル基を有する式(I)で表されるシロキサンと、2個以上のイソシアネート基を有する1種以上の化合物と、を含み、ケイ素を含まないポリオール又は前記ポリオールとイソシアネートとの反応生成物を含まないことを特徴とする組成物、ポリウレタン及びポリウレタンフォームを製造するための前記組成物の使用、前記組成物を使用して製造されたポリウレタン及びポリウレタンフォーム並びにそれらの使用に関する。
152 Sticking material for display JP2011271880 2011-12-13 JP2013125040A 2013-06-24 HYODO TOMOKI; HIRAO AKIRA; OKEYUI TAKUJI; SATODA YOSHINARI; AKAMATSU MOTOAKI; KUSAKABE NAOKI
PROBLEM TO BE SOLVED: To provide a sticking material for display that has excellent peelability and can be used repeatedly.SOLUTION: A sticking material for display includes a base material for display, and a foam layer that is provided on one side of the base material for display and has an open cell structure having through holes between adjacent spherical cells. The average hole diameter of the spherical cells is less than 20 μm; and the average hole diameter of the through holes is 5 μm or less; and the foam layer has surface openings with the average hole diameter of 20 μm or less.
153 The composite part consisting of a plastically deformable rigid polyurethane foam and the adhesive and the coating material JP2012513605 2010-06-02 JP2012528744A 2012-11-15 アレムダログル,フィクリ,エムラー; ゴンザレス,アルフォンソ パチェコ; パルトゥシュ,ゲオルク
本発明は、熱成形可能な硬質ポリウレタンフォームとライニング材料とから複合部品を製造する方法であって、熱成形可能なポリウレタンフォームを提供し、これをライニング材料に接着させることからなり、用いる接着剤が、接触して硬化する湿気硬化型ポリウレタン接着剤であり、該湿気硬化型ポリウレタン接着剤が、湿気硬化型ポリウレタン接着剤の総重量に対して少なくとも50重量%の、化学量論的に過剰な量の芳香族イソシアネートを、少なくとも二個のイソシアート反応性基を有する比較的高分子量の化合物と一個のみのイソシアネート反応性基をもつ化合物と、必要なら鎖延長剤及び/又は架橋剤とに混合して得られるイソシアネート末端プレポリマーを含むことを特徴とする方法に関する。 本発明はまた、このような方法で得られる複合部品と、その複合部品の車両中での、特に天井内張りとしての利用に関する。
【選択図】なし
154 One-component polyurethane adhesive JP2010536407 2008-11-26 JP2011505481A 2011-02-24 ウルマン,シュテファン; クラウツィク,シルビア; レーゼ,ハンス−ユルゲン
【課題】本発明は、取り扱い容易な接着剤混合物、より詳細には、建築物のための、接着を受ける部材の最適配向を可能にする接着剤混合物を提供することを目的とする。
【解決手段】上記目的は、a)ポリイソシアネートを、b)イソシアネートと反応する基を有する比較的高分子量の化合物、c)発泡剤、d)発泡調節添加剤、e)触媒、及びf)適宜に、他の添加物と混合することにより得られ、且つ、ポリイソシアネートa)をイソシアネートと反応する基よりも多くのイソシアネート基を含むような量で使用するイソシアネート基含有接着剤混合物を高圧容器から、接着されるべき少なくとも一つの物品へ施すことにより物品を接着する方法であって、発泡調節添加剤(d)がシリコンオイルを含んでおり、且つ、その接着剤混合物が減圧後に直ちにその接着領域に施される方法により達成される。
【選択図】なし
155 Packaging material for easily corrodible metal object JP2009254739 2009-11-06 JP2010111439A 2010-05-20 LEUDERS JOSEF; WACHS TILO; TRIEBERT JUERGEN
<P>PROBLEM TO BE SOLVED: To provide a packaging material requiring only a small amount of corrosion inhibitor, capable of being manufactured without applying any protection procedure at a special work time and showing a corrosion prevention effect. <P>SOLUTION: There is provided a packaging material for easily corrodible metal object that is constituted by a synthetic resin film forming an outer side part of the packaging material, an inner layer, and an adhesive agent layer connecting the synthetic resin film to the inner layer, wherein the adhesive agent layer contains volatile corrosion inhibitor and the inner layer has a high transparency for the corrosion inhibitor as compared with that of the synthetic resin outside the packaging material and the adhesive layer is formed by a reactive adhesive with which the adhesive layer is chemically hardened. <P>COPYRIGHT: (C)2010,JPO&INPIT
156 Improved adhesion between the vehicle body and fittings JP51731997 1996-09-10 JP3560983B2 2004-09-02 エー. ウォルデンバーガー,ディーン; エー. スミス,チャールズ
157 Manufacturing method of the thermal conductivity of the de minimis polyurethane rigid foam plastic JP26657390 1990-10-05 JP3216646B2 2001-10-09 オットー、フォルケルト
158 Improved adhesion between the vehicle body and fittings JP51731997 1996-09-10 JPH11508956A 1999-08-03 エー. ウォルデンバーガー,ディーン; エー. スミス,チャールズ
(57)【要約】 ポリウレタンフォームからなる感圧接着剤を、装飾部品を自動車および他の乗り物に接着するのに使用する。 その接着剤は、高い引張強さおよび伸び、優れた剥離強さ、並びに良好な熱許容度および機械的応許容度を特徴とする。
159 And a method of manufacturing the same thermosetting polyurethane structural adhesive composition JP9383390 1990-04-09 JP2590289B2 1997-03-12 CHAARUZU KODEI; TERENSU HAATOMAN
160 JPH07503037A - JP51291793 1993-01-22 JPH07503037A 1995-03-30
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