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 | Process for Production of Poly(Arylene Sulfide) | US14135219 | 2013-12-19 | US20150175748A1 | 2015-06-25 | Jeffrey S. Fodor; R. Shawn Childress; Kent E. Mitchell; Kendall M. Hurst |
| A process for producing a poly(arylene sulfide) polymer comprising (a) polymerizing reactants in a reaction vessel to produce a poly(arylene sulfide) reaction mixture, (b) processing the poly(arylene sulfide) reaction mixture to obtain a poly(arylene sulfide) polymer and a by-product slurry, (c) removing (e.g., evaporating) at least a portion of the by-product slurry to yield salt solids particulates, wherein at least a portion of the evaporating is carried out while simultaneously sizing the salt solids particulates to a desired size. | ||||||
| 222 | Isocyanurate compound for forming organic anti-reflective layer and composition including same | US13393682 | 2010-09-14 | US09063424B2 | 2015-06-23 | Hyo-Jung Roh; Dong-Kyu Ju; Hyun-Jin Kim; Deog-Bae Kim |
| An isocyanurate compound for forming an organic anti-reflective coating layer, which has superior stability and etch rate at a high temperature, and which has a high refractive index, is represented by following Formula 1. In Formula 1, R is independently a hydrogen atom or a methyl group, R1 is independently a chain type or ring type saturated or unsaturated hydrocarbyl group of 1 to 15 carbon atoms containing 0 to 6 of hetero atoms, and R2 independently a chain type or ring type saturated or unsaturated hydrocarbyl group of 1 to 15 carbon atoms containing 0 to 15 of hetero atoms, wherein, R1 can have at least two bonding parts, and in the case that R1 has at least two bonding parts, the rest parts except R1 of the compounds represented by Formula 1 can connect to the R1 to form a polymer structure. | ||||||
| 223 | Polymerizable compositions containing ethylenically unsaturated monomers having episulfide functional groups and related methods | US13864785 | 2013-04-17 | US09051426B2 | 2015-06-09 | Charles R. Hickenboth; Federico Menta; Nina V. Bojkova |
| Provided is a polymerizable composition of (a) a monomer composition including ethylenically unsaturated monomer having a β-epithiopropyl functional group; (b) optionally, a compound having two or more β-epithiopropyl functional groups but no polymerizable ethylenically unsaturated groups; (c) an isourea functional polymerization initiator; and (d) a catalyst for reaction between the β-epithiopropyl functional groups. Also provided is a method of reducing the yellowness index of a sulfur-containing polymerizate prepared by addition polymerization, the method including reacting in the presence of an isourea functional polymerization initiator and a catalyst for reaction between β-epithiopropyl functional groups, a polymerizable composition of: (a) a monomer composition including ethylenically unsaturated monomer having a β-epithiopropyl functional group; and, optionally, (b) a compound having two or more β-epithiopropyl functional groups but no polymerizable ethylenically unsaturated groups. | ||||||
| 224 | CONJUGATED POLYMER COMPOUND | US14502879 | 2014-09-30 | US20150133617A1 | 2015-05-14 | Chain-Shu HSU; Ching-Yao LIN; Chien-Lung WANG; Jhong-Sian WU; Yi-Hsiang CHAO; Jyun-Fong JHENG; Ming-Chi TSAI; Chin-Li WANG |
| A conjugated polymer compound is disclosed. The conjugated polymer compound includes a conjugated polymeric main chain; and a porphyrin compound having absorption in a blue light region of solar radiation, and is bonded to the polymeric main chain to form a side chain on the polymeric main chain. | ||||||
| 225 | Method for producing copolymer of diallylamine and sulfur dioxide | US13699885 | 2011-05-13 | US09006383B2 | 2015-04-14 | Yusuke Sato; Yusuke Fukushima; Yasuhito Nakata |
| Provided is a process for producing a copolymer of a diallylamine and sulfur dioxide which copolymer has a higher molecular weight and water-solubility than that obtained by a conventional production process by copolymerizing the diallylamine and sulfur dioxide in the presence of an acid and a radical polymerization initiator in a polar solvent. | ||||||
| 226 | CONJUGATED POLYMERS | US14385609 | 2013-02-15 | US20150076418A1 | 2015-03-19 | Nicolas Blouin; Amy Phillips; Lana Nanson; Steven Tierney; Toby Cull; Priti Tiwana; Stephane Berney; Miguel Carrasco-Orozco; Frank Egon Meyer |
| The invention relates to novel conjugated polymers comprising in their backbone one or more divalent donor units, like for example benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl (BDT), that are linked on both sides to an acceptor unit, to methods of preparing the polymers and educts or intermediates used in such preparation, to polymer blends, mixtures and formulations containing the polymers, to the use of the polymers, polymer blends, mixtures and formulations as semiconductors organic electronic (OE) devices, especially in organic photovoltaic (OPV) devices and organic photodetectors (OPD), and to OE, OPV and OPD devices comprising these polymers, polymer blends, mixtures or formulations. | ||||||
| 227 | BIS(SULFONYL)ALKANOL-CONTAINING POLYTHIOETHERS, METHODS OF SYNTHESIS, AND COMPOSITIONS THEREOF | US13923903 | 2013-06-21 | US20140378650A1 | 2014-12-25 | CHANDRA RAO; JUEXIAO CAI; RENHE LIN |
| Bis(sulfonyl)alkanol-containing polythioethers, compositions containing bis(sulfonyl)alkanol-containing polythioethers, methods of synthesizing bis(sulfonyl)alkanol-containing polythioethers and the use of bis(sulfonyl)alkanol-containing polythioethers in aerospace sealant applications are disclosed. The bis(sulfonyl)alkanol-containing polythioethers have bis(sulfonyl)alkanol groups incorporated into the backbone of the polythioether. Cured sealant compositions comprising the bis(sulfonyl)alkanol-containing polythioethers exhibit enhanced properties suitable for aerospace sealant applications. | ||||||
| 228 | Surface Modification Using Functional Carbon Nanotubes | US14031611 | 2013-09-19 | US20140363641A1 | 2014-12-11 | Jose M. Lobez Comeras |
| Techniques for CNT solubilization and surface-selective deposition via polymer-mediated assembly are provided. In one aspect, a method for self-assembly of CNTs on a substrate is provided. The method includes the following steps. One or more surfaces of the substrate are coated with a thiol-reactive compound. The substrate is contacted with carbon nanotube-polymer assemblies dispersed in a solvent, wherein the carbon nanotube-polymer assemblies include the carbon nanotubes wrapped in a polymer having side chains with thiol groups. Wherein by way of the step of contacting the substrate with the carbon nanotube-polymer assemblies, the carbon nanotube-polymer assemblies selectively bind to the surfaces of the substrate based on an interaction between the thiol groups in the polymer and the thiol-reactive compound on the surfaces of the substrate and thereby self-assemble on the substrate. | ||||||
| 229 | Surface Modification Using Functional Carbon Nanotubes | US13912417 | 2013-06-07 | US20140363638A1 | 2014-12-11 | Jose M. Lobez Comeras |
| Techniques for CNT solubilization and surface-selective deposition via polymer-mediated assembly are provided. In one aspect, a method for self-assembly of CNTs on a substrate is provided. The method includes the following steps. One or more surfaces of the substrate are coated with a thiol-reactive compound. The substrate is contacted with carbon nanotube-polymer assemblies dispersed in a solvent, wherein the carbon nanotube-polymer assemblies include the carbon nanotubes wrapped in a polymer having side chains with thiol groups. Wherein by way of the step of contacting the substrate with the carbon nanotube-polymer assemblies, the carbon nanotube-polymer assemblies selectively bind to the surfaces of the substrate based on an interaction between the thiol groups in the polymer and the thiol-reactive compound on the surfaces of the substrate and thereby self-assemble on the substrate. | ||||||
| 230 | SULFONE-CONTAINING POLYTHIOETHERS, COMPOSITIONS THEREOF, AND METHODS OF SYNTHESIS | US13833827 | 2013-03-15 | US20140275461A1 | 2014-09-18 | Chandra Rao; Juexiao Cai; Renhe Lin |
| Sulfone-containing polythioethers, compositions containing sulfone-containing polythioethers, methods of synthesizing sulfone-containing polythioethers and the use of sulfone-containing polythioethers in aerospace sealant applications are disclosed. The sulfone-containing polythioethers have sulfone groups incorporated into the backbone of the polythioether. Cured sealant compositions comprising the sulfone-containing polythioethers exhibit enhanced thermal resistance. | ||||||
| 231 | Copolythiophene semiconductors for electronic device applications | US13718308 | 2012-12-18 | US08569443B1 | 2013-10-29 | Ping Liu; Yiliang Wu; Cameron Derry; Anthony James Wigglesworth; Nan-Xing Hu |
| A semiconducting copolythiophene composition that includes repeating units obtained from the copolymerization of compounds of Formula (2): and Formula (3): in which the copolythiophene has at least two repeating units (possessing side chains, such as alkyl side chains), which are arranged in manner such that the side chains on the polythiophene backbone are distributed non-uniformly, is described. Electronic devices incorporating such copolythiophene compositions are also described. | ||||||
| 232 | ISOCYANURATE COMPOUND FOR FORMING ORGANIC ANTI-REFLECTIVE LAYER AND COMPOSITION INCLUDING SAME | US13393682 | 2010-09-14 | US20120164338A1 | 2012-06-28 | Hyo-Jung Roh; Dong-Kyu Ju; Hyun-Jin Kim; Deog-Bae Kim |
| An isocyanurate compound for forming an organic anti-reflective coating layer, which has superior stability and etch rate at a high temperature, and which has a high refractive index, is represented by following Formula 1. In Formula 1, R is independently a hydrogen atom or a methyl group, R1 is independently a chain type or ring type saturated or unsaturated hydrocarbyl group of 1 to 15 carbon atoms containing 0 to 6 of hetero atoms, and R2 independently a chain type or ring type saturated or unsaturated hydrocarbyl group of 1 to 15 carbon atoms containing 0 to 15 of hetero atoms, wherein, R1 can have at least two bonding parts, and in the case that R1 has at least two bonding parts, the rest parts except R1 of the compounds represented by Formula 1 can connect to the R1 to form a polymer structure. | ||||||
| 233 | CROSS-LINKED POLYOLS FOR CONTROLLED RELEASE FERTILIZERS | US13291698 | 2011-11-08 | US20120111077A1 | 2012-05-10 | Srirakrishna Maruvada; Nick Peter Wynnyk; Baozhong Xing |
| A controlled release fertilizer material comprising a particulate plant nutrient surrounded by a coating including a mixture of a cross-linked polyol and an isocyanate, and optionally a wax, is described. In some embodiments, the cross-linked polyol can be cross-linked with sulfur, oxygen, and/or a peroxide cross-linking moiety. In one embodiment the cross-linked polyol is castor oil cross-linked with sulfur. | ||||||
| 234 | Metal-containing compound and use thereof | US12823650 | 2010-06-25 | US07951968B2 | 2011-05-31 | Hiroshi Naruse; Atsuo Otsuji; Mitsuo Nakamura |
| A compound having two or more thiol groups and an atom selected from metal atoms in a molecule, a polythiol composition containing such a compound, a polymerizable composition containing such a polythiol composition, a resin obtained by polymerization of such a polymerizable composition, and an optical component obtained from such a resin are provided. The polymerizable composition can be a raw material for a resin having high transparency, good heat resistance and mechanical strength required for optical components such as plastic lenses and the like, while attaining a high refractive index (nd) exceeding 1.7. | ||||||
| 235 | METAL-CONTAINING COMPOUND AND USE THEREOF | US12823650 | 2010-06-25 | US20100261866A1 | 2010-10-14 | Hiroshi NARUSE; Atsuo OTSUJI; Mitsuo NAKAMURA |
| A compound having two or more thiol groups and an atom selected from metal atoms in a molecule, a polythiol composition containing such a compound, a polymerizable composition containing such a polythiol composition, a resin obtained by polymerization of such a polymerizable composition, and an optical component obtained from such a resin are provided. The polymerizable composition can be a raw material for a resin having high transparency, good heat resistance and mechanical strength required for optical components such as plastic lenses and the like, while attaining a high refractive index (nd) exceeding 1.7. | ||||||
| 236 | Polymers for delivering nitric oxide in vivo | US11500180 | 2006-08-07 | US07417109B2 | 2008-08-26 | Jonathan S. Stamler; Eric J. Toone; Richard S. Stack |
| Disclosed are novel polymers derivatized with at least one —NOx group per 1200 atomic mass unit of the polymer. X is one or two. In one embodiment, the polymer is an S-nitrosylated polymer and is prepared by reacting a polythiolated polymer with a nitrosylating agent under conditions suitable for nitrosylating free thiol groups. The polymers of the present invention can be used to coat medical devices to deliver nitric oxide in vivo to treatment sites. | ||||||
| 237 | Novel polymers for delivering nitric oxide in vivo | US11500180 | 2006-08-07 | US20070088435A1 | 2007-04-19 | Jonathan Stamler; Eric Toone; Richard Stack |
| Disclosed are novel polymers derivatized with at least one —NOx group per 1200 atomic mass unit of the polymer. X is one or two. In one embodiment, the polymer is an S-nitrosylated polymer and is prepared by reacting a polythiolated polymer with a nitrosylating agent under conditions suitable for nitrosylating free thiol groups. The polymers of the present invention can be used to coat medical devices to deliver nitric oxide in vivo to treatment sites. | ||||||
| 238 | Thiol ester compositions and processes for making and using same | US11060696 | 2005-02-17 | US20060036110A1 | 2006-02-16 | Chad Brown; Mitchell Refvik; Steven Herron |
| Thiol ester compositions, methods of making the thiol ester compositions, and methods of using the thiol ester compositions are provided. In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters and cross-linked thiol esters. The thiol ester composition can be used to produce cross-linked thiol esters, sulfonic acid-containing esters, sulfonate containing esters and thioacrylate containing esters. The thiol ester compositions can be used to produce polythiourethanes. The polythiourethanes can be used in fertilizers and fertilizer coatings. | ||||||
| 239 | Novel polymers for delivering nitric oxide in vivo | US11053593 | 2005-02-08 | US20050220756A1 | 2005-10-06 | Jonathan Stamler; Eric Toone; Richard Stack |
| Disclosed are novel polymers derivatized with at least one —NOx group per 1200 atomic mass unit of the polymer. X is one or two. In one embodiment, the polymer is an S-nitrosylated polymer and is prepared by reacting a polythiolated polymer with a nitrosylating agent under conditions suitable for nitrosylating free thiol groups. The polymers of the present invention can be used to coat medical devices to deliver nitric oxide in vivo to treatment sites. | ||||||
| 240 | Polymers for delivering nitric oxide in vivo | US10668667 | 2003-09-23 | US06875840B2 | 2005-04-05 | Jonathan S. Stamler; Eric J. Toone; Richard S. Stack |
| Disclosed are novel polymers derivatized with at least one —NOx group per 1200 atomic mass unit of the polymer. X is one or two. In one embodiment, the polymer is an S-nitrosylated polymer and is prepared by reacting a polythiolated polymer with a nitrosylating agent under conditions suitable for nitrosylating free thiol groups. The polymers of the present invention can be used to coat medical devices to deliver nitric oxide in vivo to treatment sites. | ||||||
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