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 |
|---|---|---|---|---|---|---|
| 181 | Method for producing electrolytic film | JP2003277918 | 2003-07-22 | JP2005042015A | 2005-02-17 | HASEGAWA NORIFUMI; HAYAKAWA SAI |
| PROBLEM TO BE SOLVED: To provide an electrolytic film having a gas-barrier property and heat resistance, enabling action under low moisture atmosphere and capable of keeping a proton conductivity even when used over a long period in the presence of water. SOLUTION: Condensation polymerization through dehydration of a hydrocarbon-based polymer containing a metal alkoxide and phosphoric acid is carried out in a first step to provide an intermediate product and the intermediate product is irradiated with microwave having a wavelength selectively imparting energy to a hydroxy group which the intermediate product has in a second step to provide the electrolytic film composed of a skeleton part constituted of the hydrocarbon-based polymer and phosphoric acid conducting a proton. COPYRIGHT: (C)2005,JPO&NCIPI | ||||||
| 182 | Silica gel composition, membrane electrode assembly with proton-exchange membrane and fuel cell | JP2003432663 | 2003-12-26 | JP2004307814A | 2004-11-04 | ONO MICHIO; WARIISHI KOJI; NOMURA KIMIATSU; KIKUCHI WATARU |
| <P>PROBLEM TO BE SOLVED: To provide a membrane electrode assembly with a proton-exchange membrane having a high ionic conductivity and a low methanol crossover, and to provide a fuel cell with a high output using the assembly. <P>SOLUTION: The proton-exchange membrane is specific in using a sol obtained by hydrolysis and polycondensation of precursors expressed by formulae (X) and (XI) in the presence of water and an oxidizing agent [in formula (X) L<SB>1</SB>is a (p+1)-valent linking group; R<SB>14</SB>and R<SB>15</SB>are each an alkyl group or an aryl group; n9 is 2 or 3; and p is an integer of 1-3, and in formula (XI) L<SB>2</SB>and L<SB>3</SB>are each a divalent linking group; R<SB>16</SB>-R<SB>19</SB>are each an alkyl group or an aryl group; n10 and n11 are each 2 or 3; and q is an integer of 2-4]. The assembly comprising the same membrane and the fuel cell using the assembly, are also provided. <P>COPYRIGHT: (C)2005,JPO&NCIPI | ||||||
| 183 | Proton conductive film, its manufacturing method, and fuel cell using the same | JP2002034115 | 2002-02-12 | JP2003242831A | 2003-08-29 | HONMA ITARU; SUGIMOTO TOSHIYA; NOMURA SHIGEKI |
| PROBLEM TO BE SOLVED: To provide a proton conductive film having superior heat resistance, durability, dimensional stability, flexibility, mechanical strength and fuel barrier performance and showing superior proton conductivity even at high temperatures, its manufacturing method and a fuel cell using the same. SOLUTION: The proton conductive film contains a three-dimensional crosslinked structure (A) having a silicon-oxygen bond, an organic structure (B), an amino group containing structure (C) and a proton conductive provider (D). The method of manufacturing the proton conductive film comprises a first step of preparing a mixture containing an organic silicon compound (E) having two or more hydrolytic silyl groups, an amino group containing organic silicon compound (F) having one or more hydrolytic silyl group and the proton conductive provider (D), a second step of filming the mixture, and a third step of forming the three-dimensional crosslinked structure (A) into a filed shape with hydrolysis and contraction. COPYRIGHT: (C)2003,JPO | ||||||
| 184 | Production method for reclaimed silicone-rubber product | JP2001054028 | 2001-02-28 | JP2002256078A | 2002-09-11 | YAMADA HIROSHI; YOSHIDA HITOSHI |
| PROBLEM TO BE SOLVED: To provide a production method for a reclaimed silicone-rubber product wherein the silicone rubber having properties of a high value added is reclaimed to be used. SOLUTION: The method for the reclaimed silicon rubber product comprises a pulverizing process S1 wherein a crosslinked silicone rubber is pulverized, an addition process of a crosslinking agent S2 wherein the crosslinking agent is added to the silicone raw rubber, an admixture process S3 wherein the above pulverized crosslinked silicone-rubber is admixed with the silicone raw rubber to form a mixture thereof, and a crosslinking process S5 wherein a crosslinking point is generated in the silicone raw rubber in the above mixture. | ||||||
| 185 | JPS5324112B2 - | JP13722273 | 1973-12-04 | JPS5324112B2 | 1978-07-19 | |
| 186 | JPS5240334B2 - | JP3436974 | 1974-03-27 | JPS5240334B2 | 1977-10-12 | |
| A composition curable upon exposure to ultraviolet light is disclosed which consists essentially of a vinyl-containing siloxane and siloxane-containing, silicon-bonded hydrogen atoms. A mercaptofunctional silicone can be employed in the composition as a cure accelerator. Another composition curable upon exposure to ultraviolet light which is disclosed consists essentially of a mercaptofunctional siloxane and a vinyl-containing siloxane. | ||||||
| 187 | JPS524287B2 - | JP2703074 | 1974-03-08 | JPS524287B2 | 1977-02-02 | |
| Reaction products obtained by mixing under anhydrous conditions WHERE K IS 0 TO 20 AND A is methyl or vinyl and WHERE M IS 0 TO 5 AND Y IS 1 OR 2 ARE ADHESION PROMOTERS WHICH ARE USEFUL IN PRIMER COMPOSITIONS. The primer compositions are organic solvent solutions with 50 to 99.9 weight percent organic solvent, with the balance being made up of 5 to 100 weight percent of the adhesion promoter, 0 to 50 weight percent of alkylsilicate and 0 to 50 weight percent of an organotitanate. An example of a primer composition would be a solution of 76.9 weight percent inhibited 1,1,1-trichloroethane with 23.1 weight percent of equal weight amounts of an adhesion promoter where A is vinyl, k is 3 and m has an average value of about 0.7, ethylpolysilicate and bis(acetylacetonyl)diisopropyltitanate. The primer compositions are useful in adhering room temperature vulcanizable silicone elastomers to substrates such as aluminum. | ||||||
| 188 | JPS5127706B2 - | JP1809774 | 1974-02-14 | JPS5127706B2 | 1976-08-14 | |
| 1421675 Silicone elastomers DOW CORNING CORP 20 Feb 1974 [20 Feb 1973] 7723/74 Headings C3T and C3S A RTV silicone elastomer composition is made by mixing (A) 100 p.b.w. of an hydroxylterminated polydimethylsiloxane having a viscosity of from 1000 to 100,000 cs. at 25‹ C.; (B) 5-200 p.b.w. of a filler, (C) 0-14À5 p.b.w. of an alkoxy silicon compound selected from ethylorthosilicate, n-propylorthosilicate, ethylpolysilicate and n-propylpolysilicate, (D) 0À5-10 p.b.w. of a silane of the formula wherein R is methyl, ethyl or propyl and x= 1-4, the combination of (C) and (D) providing from 1-15 p.b.w. per 100 p.b.w. of (A), and (E) 0À1-5 p.b.w. of a metal salt of a carboxylic acid wherein the metal ranges from lead to manganese in the electromotive series of metals and said carboxylic acid has less than 16 carbon atoms. Filler (B) can be a reinforcing filler such as a treated or untreated silica filler or a non-reinforcing filler. Examples of fillers are TiO 2 , CaCO 3 , ZnO, diatomaceous earth, crushed quartz; asbestos, zirconium silicate and carbon black. The preferred metal salts (E) are tin salts. In the examples compositions are prepared by mixing an OH-terminated polydimethylsiloxane (12,500 cs.), a fume silica filler surface treated to provide trimethyl siloxy units thereon, a silane of the formula dibutyltin diacetate alone and together with npropylorthosilicate, which are then cured at room temperature. The above silane is prepared by reacting betamercaptoethyl trimethoxysilane with phenylacetylene by heating first in the absence and then in the presence of azo-bis-isobutyronitrile as catalyst. | ||||||
| 189 | JPS5067333A - | JP2703074 | 1974-03-08 | JPS5067333A | 1975-06-06 | |
| Reaction products obtained by mixing under anhydrous conditions WHERE K IS 0 TO 20 AND A is methyl or vinyl and WHERE M IS 0 TO 5 AND Y IS 1 OR 2 ARE ADHESION PROMOTERS WHICH ARE USEFUL IN PRIMER COMPOSITIONS. The primer compositions are organic solvent solutions with 50 to 99.9 weight percent organic solvent, with the balance being made up of 5 to 100 weight percent of the adhesion promoter, 0 to 50 weight percent of alkylsilicate and 0 to 50 weight percent of an organotitanate. An example of a primer composition would be a solution of 76.9 weight percent inhibited 1,1,1-trichloroethane with 23.1 weight percent of equal weight amounts of an adhesion promoter where A is vinyl, k is 3 and m has an average value of about 0.7, ethylpolysilicate and bis(acetylacetonyl)diisopropyltitanate. The primer compositions are useful in adhering room temperature vulcanizable silicone elastomers to substrates such as aluminum. | ||||||
| 190 | JPS4998900A - | JP13722273 | 1973-12-04 | JPS4998900A | 1974-09-18 | |
| 191 | JPS4917413B1 - | JP10717570 | 1970-12-03 | JPS4917413B1 | 1974-04-30 | |
| 192 | テザー型有機シロキシネットワークフィルム組成物 | JP2015198979 | 2015-10-07 | JP6433875B2 | 2018-12-05 | エイドリアン・ピエール・コート; ブリン・メアリー・ドゥーリー; アンソニー・ウィグルスワース |
| 193 | 重合基体およびシリコーンポリマーの層を含む物品 | JP2015559547 | 2014-02-27 | JP6330161B2 | 2018-05-30 | ペルノ ジャン−マルク |
| 194 | 硬化性液体複合体発光ダイオード封止材 | JP2012173344 | 2012-08-03 | JP5992755B2 | 2016-09-14 | ウェイジュン・チョウ; ビンゲ・グ; ジョン・ライアンズ; アレン・エス.ブリック; ガロ・ハーナリアン; ポール・ジェイ.ポーパ; ジョン・アール.エル |
| 195 | 重合基体およびシリコーンポリマーの層を含む物品 | JP2015559547 | 2014-02-27 | JP2016516607A | 2016-06-09 | ジャン−マルク ペルノ |
| 本発明は、シリコーンポリマーの少なくとも1つの層の上に構築された少なくとも1つの重合基体を含む物品に関し、重合基体またはシリコーンポリマーの層のうちの少なくとも1つは、前記物品の構築の前に二酸化チタン、酸化マグネシウムおよび/または酸化亜鉛の粒子と接触させられ、かつ重合基体またはシリコーンポリマーの層のうちの少なくとも1つは、前記物品の構築の前または後に水と接触させられることを特徴とする。本発明はさらに、前記物品を調製する方法、ならびに重合基体とシリコーンポリマーの層との付着性を改善するための、二酸化チタン、酸化マグネシウムおよび/または酸化亜鉛の粒子の使用に関する。【選択図】なし | ||||||
| 196 | テザー型有機シロキシネットワークフィルム組成物 | JP2015198979 | 2015-10-07 | JP2016078446A | 2016-05-16 | エイドリアン・ピエール・コート; ブリン・メアリー・ドゥーリー; アンソニー・ウィグルスワース |
| 【課題】プリントヘッドフェースプレートのコーティングの湿潤防止、耐摩耗性および耐熱性を得るためにテザー型オルガノシロキサンネットワーク(OSN)フィルム組成物を提供する。 【解決手段】シロキシ官能性を有する少なくとも1つのタイプのテザー分子、シロキシ官能性を有する少なくとも1つのタイプの構築ブロックを含むオルガノシロキシネットワークフィルム組成物であって、ここでテザー分子および構築ブロックはそれぞれ同じシロキシ官能性を有し、ここでオルガノシロキシネットワークフィルムにおけるシロキシ官能性は、テザー分子および構築ブロック両方における同じシロキシ官能性から誘導される、オルガノシロキシネットワークフィルム組成物。 【選択図】なし |
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| 197 | Low-k dielectric material obtained by twin polymerization | JP2011506680 | 2009-04-28 | JP5404772B2 | 2014-02-05 | クリップ アンドレアス; ランゲ アルノ; ヘーンレ ハンス−ヨアヒム |
| 198 | Resin particles and a method of manufacturing the same | JP2011538771 | 2011-05-27 | JP5358689B2 | 2013-12-04 | 英郎 原田; 謙太 能勢; 将 本夛; 英次 岩脇; 貴博 田中 |
| Disclosed is a resin particle having excellent low-temperature fusibility, having a sufficiently narrow size distribution, and that is obtained using a liquid or supercritical fluid. In the resin particle (C), which comprises a microparticle (A) containing a resin (a) being coated to or adhered to the surface of a resin particle (B) that contains another resin (b), the degree of swelling of the microparticle (A) resulting from liquid or supercritical carbon dioxide (X) at a temperature less than the glass transition temperature or the melting point of the microparticle (A) is no greater than 16%, and with the resin (a) as a constituent unit, the resin particle (C) contains 0.1-50 wt% of a non-crystalline non-halogen vinyl monomer (m1) of which the solubility parameter (SP value: (cal/cm 3 ) 1/2 ) is 7-9. | ||||||
| 199 | Colored silicone hydrogel lens manufacturing curable colored ink | JP2007508839 | 2005-04-20 | JP5014981B2 | 2012-08-29 | フェラン，ジョン・クリストファー |
| The present invention provides an actinically or thermally curable ink for making colored silicone hydrogel contact lenses. The ink of the invention comprises at least one colorant, a solvent and a binder polymer including ethylenically unsaturated groups and segments derived from at least one silicone-containing vinylic monomer or macromer. The ink of the invention is characterized by having capability to be cured actinically or thermally to form a colored coat on a silicone hydrogel contact lens, wherein the colored coat has good adhesion to the silicone hydrogel contact lens without being covalently attached to the lens material of the contact lens. The invention also provides methods for making colored silicone hydrogel contact lenses. | ||||||
| 200 | Conductive organic containing mesoporous phase - inorganic hybrid materials, membranes, electrodes and fuel cell | JP2006502168 | 2004-01-22 | JP4963956B2 | 2012-06-27 | ヴァレ，カリン; サンチェス，クレメント; ベルヴィル，フィリップ |
| Hybrid conductive organic/inorganic material comprises a mineral phase with an open pore structure into which an oligomer or organic polymer is integrated and bonded covalently, and optionally another phase in the interior of the pores comprising a surfactant. At least one of the mineral and polymer phases has a conductive and/or hydrophilic function. Independent claims are also included for: t (1) the preparation of the material; and (2) a fuel cell comprising the material as a membrane or electrode. | ||||||
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