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 |
|---|---|---|---|---|---|---|
| 201 | METHODS OF PREPARING POLYHEMIAMINALS AND POLYHEXAHYDROTRIAZINES | US14050995 | 2013-10-10 | US20150104579A1 | 2015-04-16 | James L. Hedrick; Hans W. Horn; Gavin O. Jones; Jeannette M. O'Brien; Kumar R. Virwani |
| Polyhexahydrotriazine (PHT) film layers are formed by a process comprising heating a first mixture comprising i) a solvent, ii) paraformaldehyde, and iii) a diamine monomer comprising two primary aromatic amine groups at a temperature of about 20° C. to less than 150° C. This heating step forms a stable polyhemiaminal (PHA) in solution, which can be cast on a surface of a substrate, thereby forming an initial film layer comprising the PHA. The initial film layer is heated at a temperature of 180° C. to about 280° C., thereby converting the PHA film layer to a PHT film layer. Young's moduli of about 8 GPA to about 14 GPA have been observed for the PHT film layers. | ||||||
| 202 | SULFONIC ACID GROUP-CONTAINING POLYMER, SULFONIC ACID GROUP-CONTAINING AROMATIC COMPOUND AND METHOD OF MAKING THE SAME, AS WELL AS POLYMER ELECTROLYTE MATERIAL, POLYMER ELECTROLYTE MOLDED PRODUCT AND SOLID POLYMER FUEL CELL USING THE SAME | US14346288 | 2012-09-06 | US20150094446A1 | 2015-04-02 | Qiao Chen; Fangke Shao; Gang Wu; Daisuke Izuhara; Hiroaki Umeda |
| It is an object of the present invention to provide a sulfonic acid group-containing polymer and a sulfonic acid group-containing aromatic compound, which have excellent proton conductivity even under the low humidification condition, are excellent in mechanical strength and chemical stability and, moreover, can attain high output and excellent physical durability when processed into a solid polymer fuel cell, as well as a polymer electrolyte material, a polymer electrolyte molded product and a solid polymer fuel cell respectively using the same. The sulfonic acid group-containing polymer of the present invention is a sulfonic acid group-containing polymer comprising a constituent unit containing a sulfonic acid group (A1), and a constituent unit not containing a sulfonic acid group (A2), wherein the polymer contains a constituent unit having a specified structure as at least one constituent unit containing a sulfonic acid group (A1) at 25 mol % or more based on a sum of the constituent unit containing a sulfonic acid group (A1). Further, the polymer electrolyte material, polymer electrolyte molded product and solid polymer fuel cell of the present invention are constituted using such a sulfonic acid group-containing polymer. | ||||||
| 203 | Process for preparing polyether polyols | US14181807 | 2014-02-17 | US08987529B2 | 2015-03-24 | Klaus Lorenz; Marcus Eichmann |
| The present invention relates to a process for solvent-free preparation of polyether polyols with blockwise polyether chain structure, based on starter compounds solid at room temperature. | ||||||
| 204 | Method of forming polyaryl polymers | US13943196 | 2013-07-16 | US08962779B2 | 2015-02-24 | Matthias S. Ober |
| In a method of forming a polyacetal or polyketal, a specific acetal- or ketal-containing bis(aryl)acetal is coupled with itself or a comonomer in the presence of a catalyst and a base. The polymerization reaction tolerates hydroxyl and other functional groups on the bis(aryl)acetal. Among other applications, the polyacetals and polyketals are useful components of photoresist compositions. | ||||||
| 205 | ALKANOLYSIS PROCESS | US14372933 | 2013-01-25 | US20140378712A1 | 2014-12-25 | Suri N. Dorai; Clive Alexander Hamilton; Qun Sun |
| The present invention provides an improved process for converting a diester of polyether polyol, e.g., PTMEA, to the corresponding dihydroxy product, e.g., polytetramethylene ether glycol (PTMEG) continuously in a reaction zone, such as, for example, a reactive distillation system, for achieving virtually complete conversion of PTMEA to PTMEG, and recovery of PTMEG free of unreacted or unconverted PTMEA and alkanol ester by-product. | ||||||
| 206 | Multifunctional melamine epoxy resins, methylols and amines | US13879289 | 2012-10-31 | US08911858B2 | 2014-12-16 | Georgius Abidal Adam |
| Multifunctional melamine epoxy resins, methylols and amines are provided. Methods of making multifunctional melamine epoxy resins, methylols and amines are also provided. | ||||||
| 207 | Process for Making Hybrid Polyester-Polyether Polyols | US14365961 | 2012-12-10 | US20140357887A1 | 2014-12-04 | Pavel L. Shutov; David S. Laitar; David A. Babb |
| Hybrid polyester-polyether polyols are prepared by polymerizing an alkylene oxide in the presence of a carboxylate initiator. The polymerization is catalyzed with a mixture of double metal cyanide catalyst complex and certain magnesium, group 3-group 15 metal or lanthanide series metal compounds. | ||||||
| 208 | POLY(ARYL ETHER SULFONE) COMPOSITION AND METHOD OF MAKING | US14263063 | 2014-04-28 | US20140350207A1 | 2014-11-27 | Eric Lee Lutz; William Hoy Heath; Roy Ray Odle; Thomas Link Guggenheim; Juan Justino Rodriguez Ordonez; Jose Roman Galdamez Pena |
| 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) can have a thermal stability factor greater than or equal to 90%. The poly(aryl ether sulfone) can have a yellowness index (YI) less than 120 after an article made from the poly(aryl ether sulfone) is exposed to a temperature of 200° C. in ambient air for 28 days. The poly(aryl ether sulfone) is free of methoxy groups. Methods of making the polymer are also disclosed. | ||||||
| 209 | Crosslinked polymers with the crosslinker as therapeutic for sustained release | US13862500 | 2013-04-15 | US08889889B2 | 2014-11-18 | Rachit Ohri; Phillip Blaskovich; Joshua Kennedy; Steven L. Bennett; Arthur Driscoll |
| Crosslinked polymers, methods for their preparation and use, are described in which the crosslinked polymers are formed from at least two polymer precursors, one of which is designed, upon degradation of the crosslinked polymer, to release the second polymer precursor in its original, unmodified chemical form. | ||||||
| 210 | THIOL-SELECTIVE WATER-SOLUBLE POLYMER DERIVATIVES | US14229547 | 2014-03-28 | US20140330041A1 | 2014-11-06 | 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. | ||||||
| 211 | PROCESS FOR REDUCING UNSTABLE END-GROUPS IN FLUORINATED POLYMERS | US14359825 | 2012-11-20 | US20140309376A1 | 2014-10-16 | Marco Galimberti; Stefano Millefanti; Vito Tortelli |
| A process for reducing the number of unstable end-groups in a fluorinated polymer is disclosed, said process comprising reacting a fluorinated polymer comprising unstable end-groups with fluorine in the presence of at least one (per)haloolefin comprising at least one carbon-carbon double bond and having at least one fluorine or chlorine atom on either one of the carbon atoms of said double bond. The fluorinated polymer may be selected from those polymers comprising recurring units derived from at least one ethylenically unsaturated fluorinated monomer or from fluorinated polyethers. | ||||||
| 212 | SEMIBATCHWISE PROCESS FOR PREPARING OLEFIN-CO COPOLYMERS | US14203867 | 2014-03-11 | US20140275475A1 | 2014-09-18 | Thomas Ernst Müller; Christoph Gürtler; Walter Leitner; Henning Vogt; Saeeda Soomro |
| A process for preparing olefin-CO copolymers with the steps of: providing a reactor; charging the reactor with a gaseous olefin and with CO, such that there is a first pressure p1 in the reactor; and reacting olefin with CO in the presence of a catalyst in the reactor. Prior to the reaction, either no CO is present in the reactor or the volume ratio of gaseous olefin to CO is ≧90:10. During the reaction, gaseous olefin and CO are metered in at least intermittently, with an average over time of the volume ratio of the olefin metered into CO metered in of ≧90:10. | ||||||
| 213 | LINEAR (PER) FLUOROPOLYETHERS WITH -CF(CF3)COF END GROUPS AND DERIVATIVES THEREOF | US14349468 | 2012-09-25 | US20140243547A1 | 2014-08-28 | Simonetta Antonella Fontana; Claudio Adolfo Pietro Tonelli; Piero Gavezotti |
| The present invention relates to mono- or bi-functional (per)fluoropolyethers comprising a linear (per)fluoropolyether chain having two ends, wherein one or two ends contain —CF(CF3)COF groups, to a process for preparing them and to their use as precursors in the preparation of further functionalised (per)fluoropolyethers. The invention also relates to these further functionalised (per)fluoropolyethers. | ||||||
| 214 | (PER) FLUOROPOLYMER COMPOSITION | US14236282 | 2012-07-17 | US20140235816A1 | 2014-08-21 | Vincenzo Arcella; Claudio Adolfo Pietro Tonelli; Solange Barbieri |
| The present invention relates to (per)fluoropolymer compositions, in particular to (per)fluoropolyether compositions comprising: —a (per)fluoropolymer having more than two carboxy groups and —a polyamine. The invention further relates to processes for preparing said compositions and to moulded articles obtained from said compositions. | ||||||
| 215 | Polymer electrolyte membrane | US13890687 | 2013-05-09 | US08796412B2 | 2014-08-05 | 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. | ||||||
| 216 | GLUCOSE-PEG CONJUGATES FOR REDUCING GLUCOSE TRANSPORT INTO A CELL | US14149493 | 2014-01-07 | US20140193849A1 | 2014-07-10 | 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. | ||||||
| 217 | TELECHELIC MACROMER, METHOD FOR PRODUCING TELECHELIC MACROMER AND COMPOSITION CONTAINING TELECHELIC MACROMER | US13727859 | 2012-12-27 | US20140187663A1 | 2014-07-03 | Miroslawa EL FRAY; Jedrzej Skrobot |
| A telechelic macromer is disclosed having (meth)acrylic end-groups and a core. The macromer defined by Formula 1 comprises a core Y (Formulas 2 to 9) that is linked to (meth)acrylic groups by urethane, ester or anhydride bonds and has iodine value ranging from 5 to 75. The method involves a chemical reaction carried out in solvent, ranging 6-24 hours, wherein the precursor of a core (Formulas 2 and 3) reacts in two stages with compounds forming urethane bonds, or wherein the precursor of a core (Formulas 4 to 8) reacts in one stage with compounds forming ester bonds, or wherein the precursor of a core defined by Formula 9 reacts in one stage with compounds forming anhydride bonds. The urethane, ester and anhydride moieties comprise groups capable of free radical polymerization isolating the final product by evaporation. The composition disclosed provides the macromer, a photoinitiator and possibly a reactive diluent. | ||||||
| 218 | N-maleimidyl polymer derivatives | US13890799 | 2013-05-09 | US08765111B2 | 2014-07-01 | 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. | ||||||
| 219 | PROCESS FOR MAKING POLYETHER ALCOHOLS HAVING OXYETHYLENE UNITS BY POLYMERIZATION OF ETHYLENE CARBONATE IN THE PRESENCE OF DOUBLE METAL CYANIDE CATALYSTS | US14234577 | 2012-08-15 | US20140163197A1 | 2014-06-12 | Esther E. Quintanilla; Hanno R. Van Der Wal; Daniel C. Floyd; Myriam Linke; Francois M. Casati; Carlos M. Villa; Jean-Paul Masy; Ricco B. Borella; Paul Cookson |
| Ethylene carbonate is polymerized by itself or together with another cyclic monomer such as 1,2-propylene oxide in the presence of a double metal cyanide catalyst. Most of the ethylene carbonate adds to the chain to form a terminal carbonate group, which decarboxylates to produce a hydroxyethyl group at the end of the polymer chain. The polymerization of more ethylene carbonate onto the chain end results in the formation of poly(ethyleneoxy) units. Therefore, the process provides a method for making poly(ethyleneoxy) polymers without the need to polymerize ethylene oxide. The process is useful for making polyethers that are useful as water-absorbable polymers, surfactants and as raw materials for polyurethanes. The process is also useful for increasing the primary hydroxyl content of a polyether. | ||||||
| 220 | Thiol-selective water-soluble polymer derivatives | US13681357 | 2012-11-19 | US08722032B2 | 2014-05-13 | 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. | ||||||
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