| 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 | Flammhemmendes Vlies mit Bindefilamenten | EP90123282.7 | 1990-12-05 | EP0432620A1 | 1991-06-19 | Schöps, Michael |
Beschrieben wird ein flammhemmendes, schmelzbinderverfestigtes Spinnvlis aus tragenden Filamenten und als Schmelzbinder dienenden Binderfilamenten, wobei die Binderfilamente aus einem modifizierten Polyethylenterephthalat bestehen, in dessen Polymerkette phosphorhaltige Kettenglieder einkondensiert sind und das dadurch permanent flammhemmende Eigenschaften aufweist. |
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| 42 | Liquid crystalline polyesters | EP89201737.7 | 1989-06-30 | EP0350113A1 | 1990-01-10 | Wreesmann, Carel Theodoor Jozef; Erdhuisen, Erwin Wilhelmus Petrus |
Liquid crystalline side-chain polyesters prepared by polycondensing a dicarboxylic acid or a derivative thereof with a diol of the formula according to claim 1. Of such diols the essence is that they have a delocalized π electron system to which both an electron donor group and an electron acceptor group are coupled directly (DπA-system). Because of the structure of the diol to which the DπA-system is linked the polyesters exhibit excellent Tg and Tc values. The polyesters are to be used in optical waveguides or for optical data storage. |
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| 43 | Polyurethanes prepared from non-linear optical active diols | EP89201736.9 | 1989-06-30 | EP0350112A1 | 1990-01-10 | Wreesmann, Carel Theodoor Jozef; Erdhuisen, Erwin Wilhelmus Petrus; Sikkema, Doetze Jakob |
Polyurethanes prepared from non-linear optical active diols (NLO-diols) of the formula according to claim 1, of which the essence is that they have a delocalized π electron system to which both an electron donor group and an electron acceptor group are coupled directly (DπA system). The polyurethanes have high hyperpolarizability densities and other favourable properties and can be easily prepared. They are to be used in optical waveguides. |
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| 44 | Block copolymers comprising rubber and polyester segments, method of preparation | EP87301324.7 | 1987-02-16 | EP0242027A2 | 1987-10-21 | Kinoshita, Mitsuo; Imamura, Shigeru; Matsueda, Hirokazu |
Block copolymers comprising a liquid rubber component substituted by at least one polyester grouping, and functional derivatives thereof are advantageous additives for synthetic resins. A method for the production of the said copolymers comprises reacting a liquid rubber having one or more reactive hydrogen atoms within its molecule with at least one organic dicarboxylic anhydride and one or more species of 1,2-epoxide in the presence of catalyst. |
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| 45 | A hydrolyzable resin composition and an antifouling coating composition containing the same | EP86303760.2 | 1986-05-16 | EP0204456A1 | 1986-12-10 | Yamamori, Naoki; Ohsugi, Hiroharu; Eguchi, Yoshio; Yokoi, Junji |
A hydrolyzable resin composition based on a resin having at least one side chain bearing a particular metal containing terminal group. There is also provided an antifouling coating composition containing such a hydrolyzable resin composition as a resinous vehicle. More particularly, the resin has at least one side chain bearing at least one terminal group of the formula
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| 46 | Ionic polyesters, electrically photosensitive composite particles and materials containing the polyesters and photoelectrophoretic imaging methods | EP82400720.7 | 1982-04-22 | EP0064007B1 | 1986-01-22 | Isaacson, Henry Verschay; Regan, Michael Thomas |
| 47 | POLYESTERS CONTAINING COPOLYMERIZED, ANTHRAQUINONE COLORANT COMPOUNDS CONTAINING SULFONAMIDO GROUPS | EP84900190.0 | 1983-11-21 | EP0125311A1 | 1984-11-21 | DAVIS, Thomas, Glenn; GILES, Ralph, Rae; WEAVER, Max, Allen |
| Polyesters colorés contenant des colorants copolymérisés dérivés de l'anthraquinone et contenant un ou plusieurs groupes sulfonamido. Les polymères colorés sont résistants à la lumière et les moitiés colorantes ne peuvent en être extraites, rendant les copolymères colorés particulièrement appropriés à une utilisation dans des conteneurs pour aliments tels que des bouteilles moulées de boissons. Les viscosités inhérentes des ces polymères peuvent beaucoup varier comme cela est connu dans l'art, pour des applications différentes. Les colorants copolymérisables possèdent la formule (I), dans laquelle R1 et R2 représentent chacun l'hydrogène ou de 1 à 3 substituants sélectionnés indépendamment parmi l'alkyle, l'alkoxy et autres; et T représentent de 1 à 4 radicaux sélectionnés indépendamment de la formule (II), dans laquelle R3 représente l'hydrogène ou de 1 à 3 substituants tels que l'alkyle, l'alkoxy et autres; Z est un groupe de liaison bivalent tel que -NH-, -S-, -O-, et l'alkoxycarbonyle; et Q est un hydroxy, un carboxy ou un alkoxycarbonyle. | ||||||
| 48 | Condensation polymeric photoconductors containing pendant arylamines, photoconductive compositions and electrophotographic elements containing these photoconductors | EP82400721.5 | 1982-04-22 | EP0063528A2 | 1982-10-27 | Noonan, John Michaek; Perlstein, Jerome Howard; Isaacson, Henry Verschay; Regan, Michael Thomas |
Polymeric photoconductors comprise a condensation polymer backbone containing, as repeating units, the condensation residues of 1) a diacid and 2) an organic difunctional compound capable of undergoing condensation polymerization with said diacid, and an arylamine photoconductor group appended to at least one of said diacid or said organic difunctional compound residues. The polymeric photoconductors are useful in photoconductive compositions and electrophotographic elements. |
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| 49 | A blend of fluoro-alkyl-containing ester oligomer and polydiallyl carbodiimide (s) | JP2010511379 | 2008-06-06 | JP2010530445A | 2010-09-09 | エル．エス． エルスベルンド，シェリル; ピー． ジャリワラ，チェタン; エム． バトラー，トーマス |
| For imparting enhanced water-repellency and oil-repellency properties to substrates compositions comprising blends of (A) one or more ester oligomers and (B) one or more polycarbodiimides. Also methods for applying such compositions and articles treated with such compositions. | ||||||
| 50 | Copolymerized near infrared fluorescent compound water dissipative polyester and amide containing | JP51901594 | 1994-02-07 | JP3241732B2 | 2001-12-25 | アレン ウェバー，マックス; ロイ クッシュマン，マイケル; ジョン，シニア クラタク，ジェイムス; アルビン，ジュニア コーテス，クラレンス; フィトフィールド パーハム，ウィリアム; パトネイ，ガバー |
| 51 | Non-linear optical polymer composition, the non-linear optical materials and articles that obtained the manufacturing method, as well as from it | JP51831793 | 1993-03-10 | JP3210341B2 | 2001-09-17 | エヌ． インバセカラン，マティアー; ジェイ． グロッティ，ロバート; ピー． ハーグ，アンソニー; ジェイ． ブレナン，デビッド; イー． ベイルズ，スティーブン |
| 52 | Invisible marking / identification for organic solvent-based ink | JP52060698 | 1997-10-27 | JP2001503459A | 2001-03-13 | アレン ウェーバー，マックス; ザモーラ エスカノ，ネルソン; ジョン，シニア クルタク，ジェイムズ |
| (57)【要約】 その中に蛍光化合物を有する有機溶媒性ポリエステルインキ配合物は、インクジェット印刷応用に適している。 このインキは、識別、認証、分類等のために種々の材料の表面上に不可視印刷／マーキングを作るために有用である。 適当な印刷支持体には、プラスチック、フィルム、シート、布、紙、高光沢紙、金属、箔、板、ゴム、ガラス、セロファン、木材等のような多孔質及び非多孔質材料が含まれる。 このインキ配合物には、有機溶媒中に溶解された、その中に共重合された少なくとも１種の近赤外発蛍光団を有する、少なくとも１種の有機可溶性ポリエステルが含有されている。 適当な有機溶媒には、Ｃ 3 〜Ｃ 6炭素ケトン、Ｃ 3 〜Ｃ 6炭素有機エステル、Ｃ 1 〜Ｃ 3炭素アルコール又はこれらの組合せが含まれる。 好ましい態様に於いて、共重合された赤外発蛍光団を含有するポリエステルが、Ｃ 3 〜Ｃ 6炭素ケトン及びＣ 3 〜Ｃ 6炭素アルコールからなる溶媒に溶解されている。 | ||||||
| 53 | Liquid crystalline polyester | JP17282989 | 1989-07-04 | JP2689169B2 | 1997-12-10 | ウィルヘルムス ペトルス エルドゥイセン エルビン; テオドール ヨゼフ レースマン カレル |
| 54 | Nonlinear optical active diol and polyurethane made from it | JP17283089 | 1989-07-04 | JP2678316B2 | 1997-11-17 | ウィルヘルムス ペトルス エルドゥイセン エルビン; テオドール ヨゼフ レースマン カレル; ヤコブ シケーマ ドッゼ |
| 55 | Nonlinear optical side chain polymers having a low optical loss | JP50872493 | 1993-10-04 | JPH08506187A | 1996-07-02 | ハムス、ベルナルダス、ヘンリカス、マリア; ホフストラート、ヨハネス、ヴィレム; ムールマン、グスタフ、ロナルド |
| (57)【要約】 本発明は、低い光学減衰を示し、かつ供与体−π−受容体基を含む二官能性化合物の形のＮＬＯモノマーと、ＮＬＯモノマーに対して反応性でありかつ有機基を含む二官能性化合物の形の少なくとも一つの第一のコモノマーを反応させることによって得られうるＮＬＯ側鎖ポリマー（ここで、第一コモノマーの一部であるところの有機基中の水素原子は、より重い元素、例えば重水素又はハロゲン、特にフッ素及び／又は塩素によって置換されている）に関する。 コモノマーは、全置換されることができ、或いは、異なった置換基の２以上のコモノマーを用いることもできる。 特に、本発明は、ＤπＡ基含有ジヒドロキシ化合物、及び重水素置換された又はハロゲン化されたジヒドロキシ化合物、例えばそれ自身公知のビスクロロホルメート又はジイソシアネートから作られるＮＬＯポリエステル、ポリカーボネート及びポリウレタンに関する。 該ポリマーは、導波路、例えば、電気光学デバイス例えば光学スイッチとして用いられる。 | ||||||
| 56 | JPH06511033A - | JP50639693 | 1992-09-23 | JPH06511033A | 1994-12-08 | |
| 57 | Water-dispersible uva and/or uvb light-absorbing copolymer | JP19034693 | 1993-07-30 | JPH06145538A | 1994-05-24 | MASHIYUU EBAN RANGAA; JIYON FUREDERITSUKU HETSUSERU; FUIARIARU KAASHIYAI; DENISU SHINFUIIRUDO |
| PURPOSE: To prepare a copolymer which can absorb a broad spectrum of ultraviolet emission at the maximum wave length by polymerizing a mixture of dichloro-4,4'-stilbenedicarbonyl and specific two compounds. CONSTITUTION: The objective copolymer having a structure shown by the formula is prepared by polymerizing a mixture of dichloro-4,4'-stilbenedicarbonyl, 4,4'-dihydroxybenzophenone and chloro-2,3-dihydroxypropyltrimethylammonium. In the formula, R is a bi-functional aryl group or the like; R 1 is H or the like; R 2 is a bi-functional part which is able to absorb UVA (320 to 400 nm) light at maximum λ; R 3 is a charged part selected from carboxylic acid or the like; R 4 is a bi-functional part which is able to absorb UVB (290 to 320 nm) light at maximum λ; (x), (y), (z) and (w) are hydrophobic materials and are selected so that groups of R, R 2, R 3 and R 4 exist in the amount of 0 to 49.9, 0 to 99.9, 0.5 to 49.9 and 0 to 99.9 mole %, respectively of the polymer. COPYRIGHT: (C)1994,JPO | ||||||
| 58 | JPH03502814A - | JP50287589 | 1989-02-13 | JPH03502814A | 1991-06-27 | |
| Composition useful for molding into articles such as food containers, beverage bottles, cured structural plastics and the like comprising molding grade linear or unsaturated polyester or polycarbonate (a) containing a mono-4-acryloxystyryl or bis-4-acyloxystyryl compound or (b) having reacted therewith or copolymerized therein a styryl residue derived from a mono-4-acryloxystyryl or bis-4-acyloxystyryl compound, having the formula |
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| 59 | Liquid crystal polyester | JP17282989 | 1989-07-04 | JPH0286619A | 1990-03-27 | KARERU TEODOORU YOZEFU REESUMA; ERUBIN UIRUHERUMUSU PETORUSU E |
| PURPOSE: To obtain a liquid crystal polyester which is especially suitable for an optical data storage medium by polycondensation of a dicarboxylic acid or its derivative, and a specified diol. CONSTITUTION: This polyester is obtained by polycondensation of a dicarboxylic acid or its derivative, and a diol represented by formula I. In formula I, R 1 is a halogen atom; R 2 is OR 2, COR 2, COOR 2, CN, or CF 3; R 2 is H, or a 1-3C alkyl; Y is CR 2, C-CN, or N; A is CN, NO 2, CH=C(CN) 2, formula II, CF 3; (n) is 0-4; (x) is 0-6. It is advantageous to the polyester to use a nonlinear optically active (NLO-active) diol as a starting material. The reason is that they need not be activated before the polycondensation reaction. COPYRIGHT: (C)1990,JPO | ||||||
| 60 | Coloring polymer micro particle | JP9621289 | 1989-04-15 | JPH01311175A | 1989-12-15 | FURIIDON BEBURAA; MARIO SURONGO |
| PURPOSE: To provide a coloring polymer micro particle that contains specific dyestuff or pigment introduced by polymerization, has movement resistance, is ex in weatherability, provides highly transparent and clear color, and has good rheological property. CONSTITUTION: The micro particle is provided by polymerizing particle, which is 0.01-0.5μ in size, and is produced by copolymerizing (i) ethylene polymer or poly-unsaturated compound and/or (ii) glycidyl compound and/or (iii) poly- alcohol, poly-carboxylic acid, hydroxyl carboxylic acid, lacton, and/or amino- carboxylic acid, and dyestuff or pigment derivative represented by formula (B) (where, P is organic pigment or dyestuff group; m is 1-4, X is -OH, -NH 2, glycidyl). COPYRIGHT: (C)1989,JPO | ||||||
