| 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 | ADDITIVES TO IMPROVE OPEN-TIME AND FREEZE-THAW CHARACTERISTICS OF WATER-BASED PAINTS AND COATINGS | US13792175 | 2013-03-10 | US20140256862A1 | 2014-09-11 | Charles Francis Palmer, JR.; Lester Arnold Haney, II; Calvin M. Wicker, JR. |
| Waterborne coatings are described having an acceptable balance of properties both during the storage of coating, application and drying. The period in which irregularities in a freshly applied coating can be repaired without resulting in brush marks is referred to as the open time. Aqueous coatings generally employ dispersed high molecular weight polymers as binders. These binders often provide short open times when the coating is dried since the dispersed polymer particles tend to be immobilized quickly in the edge region of an applied coating. As a result, the viscosity of the coating increases rapidly, which leads to a limited window of workability. The instant invention provides additives that are not volatile but that will extend the time that the film is malleable after after it is applied without interfering with other attributes, such as the resistance of the coating to freezing while in the can prior to application. | ||||||
| 42 | Polymers with improved strength comprising mixed oxyalkyl units | US11415053 | 2006-05-01 | US08772421B2 | 2014-07-08 | Thomas Bachon; Andreas Ferencz; Martin Majolo; Jennifer Lambertz; Friedhelm Koepnick |
| The invention relates to compositions that are produced using a mixture from two or more polyols and to a method for producing said compositions. The invention also relates to the use of said compositions as adhesives, sealing compounds, surface-coating agents, fillers or for producing molded parts. | ||||||
| 43 | DENDRIMERS AND METHODS FOR THEIR PREPARATION | US14118620 | 2012-05-17 | US20140107376A1 | 2014-04-17 | Ian A. Tomlinson; Asghar A. Peera |
| Provided are new dendrimers and processes for making them. The dendrimers are derived from a nitroalkyloxirane compound of formula (III): wherein R1, R2, and R3 are as described herein. | ||||||
| 44 | Polymers and uses thereof | US10587419 | 2005-01-20 | US07977429B2 | 2011-07-12 | Naoshi Nagai; Masahiko Mitsuzuka; Kazuoki Nakai; Motoaki Isokawa; Shiro Nakatsuka; Daiki Taneichi; Shirou Honma; Toshimitsu Narutaki |
| Polymers having polyolefin segments as the side chain, with a structural unit represented by the following Formula (1): wherein A is an olefin polymer having a weight average molecular weight of 400 to 500,000; R is H, an alkyl group, or an aralkyl group; W and Z are each O, HN, or S; and x and y are each 0 or 1, with the proviso that at least one of them is 1. The polymer can be applied as an antistatic agent, a cosmetic additive, a releasing agent for toner, a pigment dispersant, a lubricant for vinyl chloride resins, a coating material, an emulsion composition and the like. | ||||||
| 45 | COLORANT COMPATIBLE HYDROPHOBICALLY MODIFIED POLYURETHANE THICKENER FOR PAINT | US12487297 | 2009-06-18 | US20090253832A1 | 2009-10-08 | Kirill N. BAKEEV; De-Kai Loo; Angie H. Ma; Tuyen T. Nguyen; Jeffrey K. Politis |
| A synthetic polymer has a water-soluble or water-swellable polyurethane backbone and terminal groups and/or intermediate groups of blocks of hydrophobes of alkyl- or aryl compounds containing a polymerizable cyclic monomer or a polymerizable double bond (or alkene) group or derivatives thereof. The blocks of hydrophobes are composed of two or more units of the same or different hydrophobes. These synthetic polymers are used as rheology modifiers, especially in latex paints. | ||||||
| 46 | Method for production of alkylene oxide based polymer | US11436052 | 2006-05-18 | US20060264601A1 | 2006-11-23 | Fumihide Tamura; Kazuo Takei; Teruki Matsushita; Taketo Toba |
| A method for the production of an alkylene oxide based polymer in which an alkylene oxide based polymer is obtained by allowing a monomer including one or two or more oxirane compound(s), which may have a substituent, as an essential raw material to be polymerized using a polymerization catalyst while agitating in a solvent. In this method for the production, the solvent includes one or two or more compound(s) selected from the group consisting of ketones, ketone derivatives, esters, ethers, nitrile compounds and organic halogen compounds. | ||||||
| 47 | Polymers with improved strength comprising mixed oxyalkyl units | US11415053 | 2006-05-01 | US20060194930A1 | 2006-08-31 | Thomas Bachon; Andreas Ferencz; Martin Majolo; Jennifer Lambertz; Friedhelm Koepnick |
| The invention relates to compositions that are produced using a mixture from two or more polyols and to a method for producing said compositions. The invention also relates to the use of said compositions as adhesives, sealing compounds, surface-coating agents, fillers or for producing molded parts. | ||||||
| 48 | Command-cure adhesives | US10700318 | 2003-10-31 | US20050092428A1 | 2005-05-05 | James Crivello |
| Reactive adhesive compositions that can be activated with actinic radiation, manipulated for an extended time and then cured thermally are disclosed. The prepolymer mixture for the reactive adhesive contains a catalyst component and a monomer/oligomer component. The monomer or oligomer is chosen from oxetane monomers, oxirane monomers, oxetane oligomers and oxirane oligomers. The oxirane monomers and oligomers have at least one oxygen or sulfur of an ether or thioether in a position two or three carbons removed from the oxygen of the oxirane. | ||||||
| 49 | Methods for producing a polyol and a polymer dispersed polyol | US10197528 | 2002-07-18 | US06815467B2 | 2004-11-09 | Yoshinori Toyota; Akio Horie; Hiroshi Wada; Kayoko Sugiyama; Etsuko Akagi |
| A method for producing a polyoxyalkylene polyol which comprises subjecting propylene oxide and ethylene oxide to ring-opening addition polymerization with an initiator in the presence of a catalyst, wherein the polyoxyalkylene polyol is a polyoxyalkylene polyol obtained by subjecting propylene oxide to ring-opening addition polymerization with an initiator in the presence of a double metal cyanide complex catalyst to form an oxypropylene block chain, subjecting ethylene oxide and propylene oxide to ring-opening addition polymerization randomly to form an oxyalkylene random chain, changing the catalyst and subjecting ethylene oxide to ring-opening addition polymerization in the presence of an alkali metal catalyst to form an oxyethylene block chain, and the polyoxyalkylene polyol is a polyoxyalkylene polyol having a hydroxyl value of from 5 to 56 mgKOH/g, a proportion of an initiator residue of at most 25 mass %, a proportion of the oxypropylene block chain of from 5 to 50 mass %, a total oxyethylene group content of from 5 to 60 mass %, and a ratio of primary hydroxyl groups among terminal hydroxyl groups of at least 60 mol %. | ||||||
| 50 | Methods for producing a polyol and a polymer dispersed polyol | US10197528 | 2002-07-18 | US20030100801A1 | 2003-05-29 | Yoshinori Toyota; Akio Horie; Hiroshi Wada; Kayoko Sugiyama; Etsuko Akagi |
| A method for producing a polyoxyalkylene polyol which comprises subjecting propylene oxide and ethylene oxide to ring-opening addition polymerization with an initiator in the presence of a catalyst, wherein the polyoxyalkylene polyol is a polyoxyalkylene polyol obtained by subjecting propylene oxide to ring-opening addition polymerization with an initiator in the presence of a double metal cyanide complex catalyst to form an oxypropylene block chain, subjecting ethylene oxide and propylene oxide to ring-opening addition polymerization randomly to form an oxyalkylene random chain, changing the catalyst and subjecting ethylene oxide to ring-opening addition polymerization in the presence of an alkali metal catalyst to form an oxyethylene block chain, and the polyoxyalkylene polyol is a polyoxyalkylene polyol having a hydroxyl value of from 5 to 56 mgKOH/g, a proportion of an initiator residue of at most 25 mass %, a proportion of the oxypropylene block chain of from 5 to 50 mass %, a total oxyethylene group content of from 5 to 60 mass %, and a ratio of primary hydroxyl groups among terminal hydroxyl groups of at least 60 mol %. | ||||||
| 51 | Wettable, flexible, oxygen permeable, substantially non-swellable contact lens containing polyoxyalkylene backbone units, and use thereof | US222581 | 1988-07-21 | US4857606A | 1989-08-15 | Kai C. Su; Frank F. Molock |
| Contact lenses which are optically clear, wettable, flexible, of high oxygen permeability and substantially non-swellable in the aqueous ocular environment of use, of a polymer containing polyoxyalkylene backbone units are disclosed, as well as the preparation thereof and methods of treating vision defects therewith. | ||||||
| 52 | POLYPHENYLENE SULPHIDE BLOCK COPOLYMER AND MANUFACTURING METHOD THEREFOR | EP15773574 | 2015-03-24 | EP3127941A4 | 2017-09-20 | YAMANAKA YUJI; ISAGO HIROYUKI; SAITO KEI; MATSUMOTO HIDEKI |
| A polyphenylene sulfide block copolymer contains polyphenylene sulfide units and polyorganosiloxane units and has a glass-transition temperature in the range of 80°C or lower and a weight-average molecular weight in the range of 35,000 to 100,000. Provided is a novel polyphenylene sulfide block copolymer having high flexibility as well as high heat resistance and heat aging resistance. | ||||||
| 53 | METHOD FOR PRODUCING POLYPHENYLENE ETHER ETHER KETONE | EP12804423.7 | 2012-06-22 | EP2725050A1 | 2014-04-30 | ICHINOSE, Keiko; YAMASHITA, Kohei; YOKOE, Makito; YAMAUCHI, Koji |
There is provided a production method of poly(phenylene ether ether ketone). The production method makes a cyclic poly(phenylene ether ether ketone) composition subjected to thermal ring-opening polymerization in the presence of a metal alkoxide and/or a metal phenoxide. The cyclic poly(phenylene ether ether ketone) composition includes 60% by weight or more of cyclic poly(phenylene ether ether ketone) and has a melting point of 270°C or lower. |
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| 54 | Method for producing a polyol and a polymer dispersed polyol | EP05022134.0 | 2002-07-17 | EP1632513B1 | 2009-02-18 | Toyota, Yoshinori c/o Asahi Glass Company , Ltd.; Horie, Akio c/o Asahi Glass Urethane Co., Ltd.; Wada, Hiroshi; Sugiyama, Kayoko; Akagi, Etsuko |
| 55 | NOVEL POLYMERS AND USES THEREOF | EP05703929.9 | 2005-01-20 | EP1719794A8 | 2007-02-28 | NAGAI, Naoshi, c/o Mitsui Chemicals, Inc.,; MITSUZUKA, Masahiko, c/o Mitsui Chemicals, Inc.,; NAKAI, Kazuoki, c/o Mitsui Chemicals, Inc.,; ISOKAWA, Motoaki, c/o Mitsui Chemicals, Inc.,; NAKATSUKA, Shiro, c/o Mitsui Chemicals, Inc.,; TANEICHI, Daiki, c/o Mitsui Chemicals, Inc.,; HONMA, Shirou, c/o Mitsui Chemicals, Inc.,; NARUTAKI, Toshimitsu, c/o Mitsui Chemicals, Inc., |
The present invention relates to polymers having polyolefin segments as the side chain, and uses thereof. The polymers have a structural unit represented by the following Formula (1):
Suitably, the polymer is a polymer having a unit wherein W = 0, x = 1 and y = 0 as the repeating unit, and further contains a polysiloxane block. The polymer of the invention can be applied as an antistatic agent, a cosmetic additive, a releasing agent for toner, a pigment dispersant, a lubricant for vinyl chloride resins, a coating material, an emulsion composition and the like. |
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| 56 | COLORANT COMPATIBLE SYNTHETIC THICKENER FOR PAINT | EP05711342.5 | 2005-01-07 | EP1709126A1 | 2006-10-11 | BAKEEV, Kirill, N.; LOO, De-Kai; MA, Angie, H.; NGUYEN, Tuyen, T.; POLITIS, Jeffry, K. |
| A synthetic polymer has a water-soluble or water-swellable polymer backbone and terminal groups and/or intermediate groups of blocks of hydrophobes of alkyl- or aryl compounds containing a polymerizable cyclic monomer or a polymerizable double bond (or alkene) group or derivatives thereof. The blocks of hydrophobes are composed of two or more units of the same or different hydrophobes. These synthetic polymers are used as rheology modifiers, especially in latex paints. | ||||||
| 57 | FESTIGKEITSOPTIMIERTE POLYMERE MIT GEMISCHTEN OXYALKYLENEIHEITEN | EP04790383.6 | 2004-10-14 | EP1678254A1 | 2006-07-12 | BACHON, Thomas; LAMBERTZ, Jennifer; FERENCZ, Andreas; KÖPNICK, Friedhelm; MAJOLO, Martin |
| The invention relates to compositions that are produced using a mixture from two or more polyols and to a method for producing said compositions. The invention also relates to the use of said compositions as adhesives, sealing compounds, surface-coating agents, fillers or for producing molded parts. | ||||||
| 58 | COMMAND-CURE ADHESIVES | EP04779597.6 | 2004-07-29 | EP1651700A1 | 2006-05-03 | CRIVELLO, James, V. |
| Reactive adhesive compositions that can be activated with actinic radiation, manipulated for an extended time and then cured thermally are disclosed. The prepolymer mixture for the reactive adhesive contains a catalyst component and a monomer/oligomer component. The monomer or oligomer is chosen from oxetane monomers, oxirane monomers, oxetane oligomers and oxirane oligomers. The oxirane monomers and oligomers have at least one oxygen or sulfur of an ether or thioether in a position two or three carbons removed from the oxygen of the oxirane. | ||||||
| 59 | Procédé pour la fabrication de polymères d'halogénures de vinyle modifiés par des polymères de composés hétérocycliques oxygénés | EP87201699.3 | 1987-09-08 | EP0264982A1 | 1988-04-27 | Malfroid, Pierre; Nguyen, Qui Long; Blondin, Jean-Marie |
Dans une première étape, on polymérise par voie ionique un composé hétérocyclique oxygéné dans un halogénure de vinyle et, dans une seconde étape, on polymérise par voie radicalaire en dispersion aqueuse et en présence du milieu de polymérisation provenant de l'étape première l'halogénure de vinyle, éventuellement additionné d'autres monomères insaturés polymérisables par voie radicalaire. |
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| 60 | 通気性貼り合わせフィルムおよびその製造方法 | JP2016507887 | 2014-04-09 | JP2016522103A | 2016-07-28 | テ フーン キム，; ヨン ウーク キム， |
| 本発明は、ウイルス遮断保護服、自動車塗膜保護フィルムおよびスポーツウェアなどに適用可能な通気性貼り合わせフィルムに関し、不織布、メッシュフィルムまたは繊維織物などの補強フィルムと通気性フィルムを通気性ポリウレタン樹脂接着剤で貼り合わせて強度を向上させ、透気度を維持するように製造された通気性貼り合わせフィルムに関する。【選択図】なし | ||||||
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