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 |
|---|---|---|---|---|---|---|
| 221 | Chemically resistant membranes, coatings and films and methods for their preparation | US13202303 | 2010-02-21 | US08710109B2 | 2014-04-29 | Charles Linder; Ora Kedem; Yoram Oren |
| There is provided herein a membrane or film comprising one or more aromatic ionomers covalently crosslinked through aryl-aryl (—Ar—Ar—), aryl-ether-aryl (—Ar—O—Ar—), aryl-sulfide-aryl (—Ar—S—Ar—), aryl-sulfone-aryl bonds, or any combination thereof, wherein said one or more aromatic ionomers further comprises at least one electron withdrawing group adapted to improve oxidant resistance of said membrane or film. | ||||||
| 222 | TRIAZINE CONTAINING FLUOROPOLYETHER ELASTOMERS HAVING LOW GLASS TRANSITION TEMPERATURE | US14003141 | 2012-02-24 | US20140073737A1 | 2014-03-13 | Miguel A. Guerra; Rudolf J. Dams; Steven G. Corveleyn |
| There is provided a curable composition comprising: a) fluoropolyethers having a molecular weight of from about 400 g/mole up to about 20,000 g/mole and containing moieties selected from (—(CF2)4O—), (—(CF2)2O—), (—CF2O—) or combinations thereof and further containing at least one nitrile group at a terminal position or at a position that is adjacent to the terminal position; and b) one or more curing agents selected from non-fluorinated compounds containing one or more functional group linked to a common residue, said residue containing at least three carbon atoms wherein the functional groups are selected from primary amines, secondary amines and functional groups that generate primary or secondary amines upon heat treatment, wherein the composition can be cured by generating groups having a triazine structure. Also provided are cured composition, methods of making cured compositions, articles made by curing the cured compositions and methods of making articles using the curable composition. | ||||||
| 223 | ALKYL ETHER COMPOSITIONS AND METHODS OF USE | US13761512 | 2013-02-07 | US20140039214A1 | 2014-02-06 | William B. CARLSON; Gregory D. Phelan |
| A polymer includes a linker represented by Formula I ([OR1OCH2OR2OCH2]m), where R1 and R2 are, independently, alkylene, alkenylene, arylene, heteroarylene, or alkylarylalkylene; and the polymer has a weight average molecular weight of about 500 g/mol to about 2,000,000 g/mol, and m is 1 to 1000. | ||||||
| 224 | MONO-LAYER THIN FILM ADHESIVE COMPOUNDS AND METHODS OF SYNTHESIS AND USE | US13951182 | 2013-07-25 | US20140030944A1 | 2014-01-30 | John L. Murphy; Jeffrey L. Dalsin; Arinne N. Lyman; Laura L. Vollenweider; Joel L. Broussard; Neil Winterbottom; Justin T. Koepsel |
| The invention relates provides synthetic medical adhesives which exploit plant derivatives to form covalent bonds with amines and thiols on tissue surfaces. | ||||||
| 225 | ACETAL METATHESIS POLYMERIZATION | US14034839 | 2013-09-24 | US20140024801A1 | 2014-01-23 | STEPHEN A. MILLER; ALEXANDER G. PEMBA |
| A method of preparing a polyacetal comprising polymerization of a mixture comprising a plurality of at least one bis-acetal monomer in the presence of an acid catalyst that promotes the metathesis of the acetal units. The bis-acetal can be formed from an acid catalyzed exchange between a mono-acetal monomer with a diol. The formation of the bis-acetal and the polyacetal can be carried out simultaneously. The diol can be isolated from a biorenewable source and the ultimate polyacetal is a degradable or biodegradable polymer. | ||||||
| 226 | Compositions for Containers and Other Articles and Methods of Using Same | US13570743 | 2012-08-09 | US20130316109A1 | 2013-11-28 | Jeffrey Niederst; Richard H. Evans; Robert M. O'Brien; Kevin Romagnoli; Mark S. Von Maier |
| This invention provides a polymer, which is preferably a polyether polymer. The polymer may be uses in coating compositions. Containers and other articles comprising the polymer and methods of making such containers and other articles are also provided. The invention further provides compositions including the polymer (e.g., powder coatings), which have utility in a variety of coating end uses, including, for example, valve and pipe coatings. | ||||||
| 227 | SURFACTANT COMPOSITIONS AND USE FOR AQUEOUS COMPOSITIONS | US13865272 | 2013-04-18 | US20130280434A1 | 2013-10-24 | Irina V. Graf; Arkady L. Krasovskiy |
| A surfactant composition selected from the group consisting of: ArO—(CH2CH[CH2CH3]O)1-10(CH2CH2O)5-50H, isomers, aromatic ring substituted analogues, and mixtures thereof; and an aqueous coating composition including an aqueous polymeric dispersion, and certain other compositions, including the surfactant composition are provided. Also provided are a method for forming a coating and a method for improving the freeze/thaw stability of an aqueous composition including an aqueous polymeric dispersion. | ||||||
| 228 | N-MALEIMIDYL POLYMER DERIVATIVES | US13890799 | 2013-05-09 | US20130253207A1 | 2013-09-26 | Xiaoming SHEN |
| The invention is directed to multi-functional N-maleimidyl polymer derivatives comprising a water soluble and non-peptidic polymer backbone having a terminal carbon, such as a poly(alkylene glycol), the terminal carbon of the polymer backbone being directly bonded to the nitrogen atom of a N-maleimidyl moiety without a linking group therebetween. The invention also provides two methods of preparing such linkerless N-maleimidyl polymer derivatives. | ||||||
| 229 | CHEMICALLY RESISTANT MEMBRANES, COATINGS AND FILMS AND METHODS FOR THEIR PREPARATION | US13202303 | 2010-02-21 | US20130203873A1 | 2013-08-08 | Charles Linder; Ora Kedem; Yoram Oren |
| There is provided herein a membrane or film comprising one or more aromatic ionomers covalently crosslinked through aryl-aryl (—Ar—Ar—), aryl-ether-aryl (—Ar—O—Ar—), aryl-sulfide-aryl (—Ar—S—Ar—), aryl-sulfone-aryl bonds, or any combination thereof, wherein said one or more aromatic ionomers further comprises at least one electron withdrawing group adapted to improve oxidant resistance of said membrane or film. | ||||||
| 230 | Polymer electrolyte membrane | US13061600 | 2009-11-04 | US08461287B2 | 2013-06-11 | Seong-Ho Choi; Won-Ho Lee |
| Disclosed are a multi-block copolymer, its producing method and an electrolyte membrane using the same. The multi-block copolymer includes a hydrophobic block having a plurality of repeating units represented as chemical formula 1; and a hydrophilic block having a plurality of repeating units represented as chemical formula 2. The multi-block copolymer is acidified, and can be used to an electrolyte membrane and a fuel cell. The use of the multi-block copolymer as an electrolyte membrane ensures excellent dimensional stability. | ||||||
| 231 | POLY(ARYL ETHER SULFONE) COMPOSITION, AND METHOD OF MAKING | US13285043 | 2011-10-31 | US20130109831A1 | 2013-05-02 | Eric Lee Lutz; William Hoy Heath; Roy Ray Odle; Thomas Link Guggenheim |
| A poly(aryl ether sulfone) comprises units of formula (I): wherein Ar1 is a divalent C6-C15 aromatic group, Ar2 is a divalent C6-C15 aromatic group, Ar3 is a divalent C6-C15 aromatic group, and n is greater than 1; and a terminal group of formula (II) derived from a monofunctional phenoxide wherein is X is a hydrogen atom or an organic substituent having from 1 to 20 carbon atoms; wherein the poly(aryl ether sulfone) has a hydroxyl group content greater than 0 and less than 50 parts per million (ppm), based on the poly(aryl ether sulfone) weight, a glass transition temperature of 180 to 290° C., a weight average molecular weight of 20,000 to 100,000, a halogen content of greater than 0 and less than 3000 ppm based on the poly(aryl ether sulfone) weight. The poly(aryl ether sulfone) is free of methoxy groups. | ||||||
| 232 | Ionic viscoelastics and viscoelastic salts | US12297756 | 2007-04-20 | US08367845B2 | 2013-02-05 | Mark W. Grinstaff; Michel Wathier |
| One embodiment of the present invention relates to ionic liquids and ionic viscoelastics formed between [1] a small molecule or macromolecule containing two or more cations; and [2] a small molecule or macromolecule containing two or more anions. Another embodiment of the invention is the use of the inventive ionic liquids and ionic viscoelastics, formed between a small molecule or macromolecule containing two or more cations and a small molecule or macromolecule containing two or more anions, to form a crosslinked network. In certain embodiments, the ionic liquids formed can be viscous liquids, viscous liquid formed networks, or viscoelastic networks/gels. In certain embodiments, the ionic material of the invention may be used for a variety of applications including, but not limited to, lubricants, additives, gas separation, liquid separation, membranes, fuel cells, sensors, batteries, coatings, heat storage, liquid crystals, biocompatible fluids, solvents, and electronic materials. | ||||||
| 233 | POLYFUNCTIONAL POLYOXYALKYLENE COMPOUND, AND PRODUCING METHOD AND INTERMEDIATE THEREOF | US12830746 | 2010-07-06 | US20110245509A1 | 2011-10-06 | Ken-ichiro NAKAMOTO; Masaki KAMIYA; Tsuyoshi TAKEHANA |
| A polyfunctional polyoxyalkylene compound represented by the following formula (1): wherein Z represents a hydroxyl group-removed residue of pentaerythritol or dipentaerythritol, R represents a hydrocarbon group having 1 to 24 carbon atoms, OA1 and OA2 represent an oxyalkylene group having 2 to 4 carbon atoms, L1 and L2 represent an alkylene group which may have an ester bond or the like in the alkylene chain or at the terminal end, and X represents a functional group capable of reacting chemically; R, OA1, OA2, L1, and L2 are the same or different from one another in one molecule, m and n are an average number of moles of the oxyalkylene group added, m represents 5 to 1,000, and n represents 0 to 1,000; p and q represent 0 or 1; r1+r2=4 or 6; and r1 and r2 are an integer of 2 or more. | ||||||
| 234 | GLUCOSE-PEG CONJUGATES FOR REDUCING GLUCOSE TRANSPORT INTO A CELL | US13139170 | 2009-12-11 | US20110243851A1 | 2011-10-06 | Karthikeyan Narayanan; Andrew Chwee Aun Wan; Jackie Y. Ying; Nandanan Erathodiyil |
| There is provided a glucose-PEG conjugate comprising a PEG moiety conjugated to a linear glucose moiety at the C1 position of the glucose moiety. The glucose-PEG conjugate may be used to reduce glucose transport into a cell and may be used to treat a proliferative disorder. | ||||||
| 235 | Block copolymer and application thereof | US10531265 | 2003-10-14 | US07910686B2 | 2011-03-22 | Hiroshi Shinoda; Atsushi Terahara |
| The present invention relates to a block copolymer having at least one block having an acid group and at least one block having substantially no acid group, wherein one end group of a repeating unit in at least one block of all blocks is oxygen and/or sulfur, and at least one repeating unit of a block having substantially no acid group contains a halogen atom. The block copolymer of the present invention gives a polymer electrolyte membrane which is excellent not only in heat resistance and proton conductivity but also in water resistance and chemical stability, and is useful as an electrolyte for a proton conducting membrane etc. of a fuel cell. | ||||||
| 236 | Thiol-Selective Water-Soluble Polymer Derivatives | US12909755 | 2010-10-21 | US20110034643A1 | 2011-02-10 | Antoni Kozlowski; Remy F. Gross, III; Samuel P. McManus |
| The present invention provides water-soluble, polymer derivatives having a thiol-selective terminus suitable for selective coupling to thiol groups, such as those contained in the cysteine residues of proteins, as well as methods for preparing the water-soluble, polymer derivatives having a thiol-selective terminus. | ||||||
| 237 | Catalytic conversion of amide compounds to methyl ether polymers and methyl ether ladder polymers | US12317796 | 2008-12-29 | US20100168377A1 | 2010-07-01 | Melvin Keith Carter |
| Catalytic processes have been developed for direct chemical conversion of amides to methyl ether polymers or methyl ether ladder polymers. Amides formed by reacting acetic acid with monoethanol amine (MEA) or acetic acid with butylamine were polymerized in the presence of transition metal catalysts in air to form linear polymers. Ethanol acetamide was catalytically converted to a linear polyether as characterized by FTIR spectra. The catalysts were based on molecular strings of mono-, di- or tri-valent transition metal compounds that opened the amide carbonyl double bond to produce linear polyethers. Laboratory results have demonstrated [cobalt(II)]2, [manganese(II)]2, cobalt(II)-manganese(II), [nickel(II)]2 and related families of catalysts to be effective for formation of methyl ether polymers by this process.Similar transition metal catalysts plus hydrogen peroxide facilitated reactions of the amide compounds dimethylacetamide (DMAc), DMF as well as amides formed from L-cysteine with MEA, serine with MEA, arginine with MEA and histidine with MEA to form insoluble methyl ether ladder polymers at or near ambient temperature that were quite different from the linear polyether polymers. Catalysts active for these polymerizations were based on di- or tri-valent transition metals. The polymer formed from DMAc using a Co(III) catalyst plus 20% hydrogen peroxide was a ladder polymer as characterized by FTIR spectroscopy and isolated solids were observed to be microscopic hexagonal needle shaped crystals. The catalysts were based on molecular strings of tri-valent transition metal compounds. Laboratory results have demonstrated [cobalt(III)]2 and related families of catalysts in the presence of hydrogen peroxide to be effective for formation of methyl ether ladder polymers. | ||||||
| 238 | Polymerizable composition containing an odor masking agent and a perfume, an optical lens and a production method | US11571142 | 2005-06-21 | US07618141B2 | 2009-11-17 | Chefik Habassi; Alexandra Roos; Leang Ly |
| The invention relates to a composition comprising one or more polymerizable monomers, comprising at least one masking agent selected amongst cyclic ethers and at least one perfume selected amongst naturally occurring musks and extracts thereof, synthetic musks, and mixtures thereof. | ||||||
| 239 | COVALENTLY FUNCTIONALIZED PARTICLES FOR SYNTHESIS OF NEW COMPOSITE MATERIALS | US12404172 | 2009-03-13 | US20090240013A1 | 2009-09-24 | Richard B. Timmons; Dattatray Wavhal; Dhiman Bhattacharyya; Narayan Mukherjee |
| The present invention includes compositions and methods for synthesis of composite materials involving gas phase plasma polymerization to covalently plasma graft an organic molecule onto particles; covalently binding an organic monomer to the functionalized particles; and, polymerizing the organic monomers into hybrid polymer composite materials. | ||||||
| 240 | Method of preparing aliphatic polymer having ketone group in main chain thereof and method of preparing composition containing the same | US10568428 | 2004-04-30 | US07576172B2 | 2009-08-18 | Taishi Shigematsu; Chikara Manabe; Masaki Hirakata; Kentaro Kishi; Miho Watanabe; Hiroyuki Watanabe |
| The present invention discloses a method of synthesizing an aliphatic polymer having a ketone group in the main chain thereof, in which polyhydric alcohol (for example, glycerin) as a raw material is polymerized in the presence of a catalyst, and a method of preparing a composition containing an aliphatic polymer having a ketone group in the main chain thereof, including such a process. | ||||||
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