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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 2070. Отображено 100.
13-06-2013 дата публикации

HIGHLY HEAT RESISTANT AND HIGHLY STRONG ACRYLIC COPOLYMER, A RESIN COMPOSITION COMPRISING THE SAME AND AN OPTICAL FILM AND AN IPS MODE LIQUID CRYSTAL DISPLAY DEVICE COMPRISING THE SAME

Номер: US20130150546A1
Принадлежит: LG CHEM ,LTD.

Provided is an acrylic copolymer comprising; an alkyl (meth)acrylate monomer; a monomer comprising a cyclic pendant structure; and a tert-butyl (meth)acrylate monomer and/or (meth)acrylamide monomer. Also provided is a resin composition comprising the same and an optical film and an IPS mode liquid crystal display device using the same. 1. An acryl-based copolymer comprising:an alkyl (meth)acrylate-based monomer;a monomer comprising a cyclic pendant structure; anda tert-butyl (meth)acrylate-based monomer.2. The acryl-based copolymer of claim 1 , further comprising a (meth)acrylamide-based monomer.3. The acryl-based copolymer of claim 1 , wherein the alkyl (meth)acrylate-based monomer has an alkyl group having a carbon number of 1-10.4. The acryl-based copolymer of claim 1 , wherein the alkyl (meth)acrylate-based monomer is methyl (meth)acrylate.5. The acryl-based copolymer of claim 1 , wherein the monomer comprising the cyclic pendant structure is styrene-based monomer.6. The acryl-based copolymer of claim 5 , wherein the styrene-based monomer is one or more selected from the group consisting of styrene claim 5 , α-methylstyrene claim 5 , 3-methylstyrene claim 5 , 4-methylstyrene claim 5 , 2 claim 5 ,4-dimethylstyrene claim 5 , 2 claim 5 ,5-dimethylstyrene claim 5 , 2-methyl-4-chlorostyrene claim 5 , 2 claim 5 ,4 claim 5 ,6-trimethylstyrene claim 5 , cis-β-methylstyrene claim 5 , trans-β-methylstyrene claim 5 , 4-methyl-α-methylstyrene claim 5 , 4-fluoro-α-methylstyrene claim 5 , 4-chloro-α-methylstyrene claim 5 , 4-bromo-α-methylstyrene claim 5 , 4-t-butylstyrene claim 5 , 2-fluoro styrene claim 5 , 3-fluorostyrene claim 5 , 4-fluorostyrene claim 5 , 2 claim 5 ,4-difluorostyrene claim 5 , 2 claim 5 ,3 claim 5 ,4 claim 5 ,5 claim 5 ,6-pentafluorostyrene claim 5 , 2-chlorostyrene claim 5 , 3-chlorostyrene claim 5 , 4-chlorostyrene claim 5 , 2 claim 5 ,4-dichlorostyrene claim 5 , 2 claim 5 ,6-dichlorocstyrene claim 5 , octachlorostyrene claim 5 , 2-bromostyrene claim ...

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27-06-2013 дата публикации

RESIN COMPOSITION FOR GOLF BALL AND GOLF BALL

Номер: US20130165263A1
Принадлежит: DUNLOP SPORTS CO. LTD.

The present invention provides a resin composition for a golf ball and a golf ball which have high resilience while maintaining soft compression and also have low spin on driver shots, and therefore can achieve a long flight distance. The present invention relates to a resin composition for a golf ball, including an ionomer resin consisting of a metal ion-neutralized copolymer of (A) a Cα,β-unsaturated carboxylic acid and (B) a Cα,β-unsaturated carboxylic acid ester, the ionomer resin having a mass ratio of (A)/(B) of 10/90 to 25/75, and a degree of neutralization of 30 to 105 mol %. 1. A resin composition for a golf ball , comprising an ionomer resin consisting of a metal ion-neutralized copolymer of (A) a Cα ,β-unsaturated carboxylic acid and (B) a Cα ,β-unsaturated carboxylic acid ester ,the ionomer resin having a mass ratio of (A)/(B) of 10/90 to 25/75, and a degree of neutralization of 30 to 105 mol %.2. The resin composition for a golf ball according to claim 1 ,wherein the mass ratio of (A)/(B) is 15/85 to 25/75.3. The resin composition for a golf ball according to claim 1 ,wherein the ionomer resin has a degree of neutralization of 50 to 105 mol %.4. The resin composition for a golf ball according to claim 1 ,wherein the (A) is at least one of an acrylic acid and a methacrylic acid, and the (B) is at least one of an acrylic acid ester and a methacrylic acid ester.5. The resin composition for a golf ball according to claim 1 ,wherein the metal ion is a magnesium ion.6. The resin composition for a golf ball according to claim 1 ,{'sub': '3-8', 'wherein the Cα,β-unsaturated carboxylic acid (A) is selected from the group consisting of an acrylic acid, a methacrylic acid, a fumaric acid, a maleic acid, and a crotonic acid.'}7. The resin composition for a golf ball according to claim 1 ,{'sub': '3-8', 'wherein the Cα,β-unsaturated carboxylic acid ester (B) is selected from the group consisting of methyl, ethyl, propyl, n-butyl, or isobutyl esters of an acrylic ...

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04-07-2013 дата публикации

METHODS FOR SYNTHESIS OF POLYMACROMOLECULES AND POLYMACROMOLECULAR BRUSHES

Номер: US20130171461A1

In one aspect, the present invention is directed to methods for fabricating multilayer polymacromer compositions. In some embodiments, the multilayer polymacromer compositions described herein can comprise heterobifunctional macromolecules and heterotrifunctional molecules. 1. A method for generating a multilayer polymacromer composition , the method comprising:(a) functionalizing a substrate with a primer surface group to form a functionalized substrate layer,(b) covalently linking a linker to the primer surface group, wherein the linker comprises a photocleavable functionality and a click moiety terminus,(c) forming a monomolecular layer by contacting the click moiety terminus of the linker with a first heterobifunctional macromolecule comprising a polymer backbone, a first click moiety terminus and a protected second click moiety terminus,(d) deprotecting the protected second click moiety terminus to form a functionalized monomolecular layer and,(e) forming a second monomolecular layer by contacting the functionalized monomolecular layer with a second heterobifunctional macromolecule comprising a polymer backbone, a first click moiety terminus and a protected second click moiety terminus, or a first heterotrifunctional branch comprising a first click moiety group and at least two protected second click moiety groups.2. The method of claim 1 , further comprising the step of repeating steps (c) to (e) until a multilayer polymacromer composition comprising (i) a primer surface layer comprising a linker claim 1 , wherein the linker comprises a photocleavable functionality claim 1 , (ii) a monomolecular layer comprising a heterobifunctional macromolecule claim 1 , and (iii) a desired number of monomolecular layers between the linker and a surface monomolecular layer is obtained.3. The method of claim 1 , further comprising removal of the multilayer polymacromer composition from the substrate claim 1 , wherein removal is achieved by irradiation of the photocleavable ...

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29-08-2013 дата публикации

"Motor vehicle part made of surface-treated material based on polymer(s)"

Номер: US20130223086A1
Принадлежит: VALEO VISION

A motor vehicle part comprising a material based on polymer(s), the material being surface treated by ion bombardment in order to improve the surface appearance of the material. The invention also relates to a process for obtaining this part and the use thereof, in particular for the manufacture of lighting and/or signaling devices. 1. A motor vehicle part comprising a material based on polymer(s) , having a superficial thickness that has increased crosslinking.2. The motor vehicle part according to claim 1 , wherein said superficial thickness has a reduction in the fraction of the free volume of the material.3. The motor vehicle part according to claim 1 , capable of being obtained by the process comprising the step:a. treating a surface of the material of the part by ion bombardment.4. The motor vehicle part according to claim 1 , in which said superficial thickness is less than 5 μm starting from one surface of the material.5. The motor vehicle part according to claim 1 , in which the polymer(s) is/are selected from the group consisting of polycarbonates (PC) claim 1 , high-temperature polycarbonates (PC-HT) claim 1 , polyamides (PA) claim 1 , polypropylenes (PP) and polymethyl methacrylates (PMMA).6. The motor vehicle part according to claim 1 , also comprising a reflective layer on an outer surface of said material.7. The motor vehicle part according to claim 1 , said part being a part of a lighting and/or signaling device.8. The motor vehicle part according to claim 7 , wherein said part is a reflector.9. The motor vehicle part according to claim 7 , said part being a style part claim 7 , such as a bezel.10. The motor vehicle part according to claim 1 , said polymer having a Young's modulus at 23° C. of greater than 100 MPa (100 megapascals).11. A process for treating a motor vehicle part comprising a material based on polymer(s) claim 1 , in which a step of ion bombardment of an outer surface of the material is carried out.12. The process according to claim ...

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26-09-2013 дата публикации

OXAZOLINYL-CONTAINING POLYMERS AND GRAFTED COMPOUNDS PREPARED FROM THE OXAZOLINYL-CONTAINING POLYMERS

Номер: US20130253137A1
Принадлежит: 3M INNOVATIVE PROPERTIES COMPANY

Oxazolinyl-containing compounds having a single oxazolinyl group plus a first polymeric group are described. Grafted compounds are also described that are the product of a reaction of an oxazolinyl-containing compound with a second compound that has one or more acidic groups to form a grafted compound. In some embodiments, the second compound is a polymeric material having at least one acidic group and the reaction product is a grafted copolymer. Blended compositions of the grafted copolymer with a polyamide are also described. 2. The compound of claim 1 , wherein the group Q has a weight average molecular weight equal to at least 5000 grams/mole.3. The compound of claim 1 , wherein the compound has a glass transition temperature equal to at least 20° C.4. (canceled)5. (canceled)6. The compound of claim 1 , wherein Ris phenylene.7. The compound of claim 1 , wherein Ris an alkylene or a single bond.8. The compound of claim 1 , wherein Ris a heteroalkylene.10. The reaction mixture of claim 9 , wherein the second compound is a polymeric material having multiple acidic groups.11. The reaction mixture of claim 9 , wherein the second compound is a second polymeric material having multiple carboxyl groups.12. (canceled)14. (canceled)15. The grafted copolymer of claim 13 , wherein the grafted copolymer has a plurality of pendant groups of formula —(CO)OC(R)C(R)NH—(CO)—R—(CO)—NH—C(R)C(R)—O(CO)-Q.16. The grafted copolymer of claim 13 , wherein the group Q is phase separated from the second polymeric material of the grafted copolymer.18. The composition of claim 17 , wherein the composition is hot melt processable.19. (canceled)20. The composition of claim 17 , wherein polyamide is present in an amount in a range of 0.5 to 20 weight percent based on a total weight of the composition. This application claims the benefit of U.S. Provisional Patent Application No. 61/422,743, filed Dec. 14, 2010, the disclosure of which is incorporated by reference herein in its entirety. ...

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17-10-2013 дата публикации

Acrylic pressure-sensitive adhesive composition and acrylic pressure-sensitive adhesive tape

Номер: US20130274419A1
Принадлежит: Nitto Denko Corp

An acrylic pressure-sensitive adhesive composition contains: an acrylic polymer (A); and a (meth)acrylic polymer (B) that includes, as a monomer unit, a (meth)acrylic monomer having a tricyclic or higher alicyclic structure and that has a weight average molecular weight of 1000 or more and less than 30000.

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07-11-2013 дата публикации

ROUTES TO POLYACRYLATES

Номер: US20130296454A1
Принадлежит:

A polyacrylate is obtained by radical polymerization of at least one acrylate monomer (Ac) in the presence of a polymeric photoinitiator. The polymeric photoinitiator is a co-polymer of at least one photoinitiator monomer (A) with at least one monomer (B), and optional additional monomers (C). Rapid polymerization of the acrylate monomer is provided. A method produces a polyacrylate using the polymeric photoinitiator as described, and a polymeric photoinitiator is used as the photoinitiator of radical polymerization of acrylate monomers. 2. A polyacrylate according to claim 1 , wherein Wand Ware independently selected from alcohol claim 1 , primary amine claim 1 , secondary amine or thiol groups claim 1 , preferably alcohol groups.3. A polyacrylate according to claim 1 , wherein Wand Ware the same functional groups.4. A polyacrylate according to claim 1 , wherein Xand Xare independently selected from optionally substituted C-Calkylene claim 1 , —O— claim 1 , —S— claim 1 , —NR— claim 1 , wherein Ris H or optionally substituted C-Calkyl claim 1 , and combinations thereof.5. A polyacrylate according to claim 1 , wherein Xand Xmay be linked to one another to form one or more ring structures.6. A polyacrylate according to claim 1 , wherein Xand Xare independently selected from optionally substituted C-Calkylene claim 1 , preferably optionally substituted C-Calkylene.7. A polyacrylate according to claim 1 , wherein Xand Xare the same.8. A polyacrylate according to claim 1 , wherein Z is selected from a single bond claim 1 , optionally substituted C-Calkylene claim 1 , optionally substituted C-Calkenylene claim 1 , —O— claim 1 , —S— claim 1 , —NR— claim 1 , —C(═O)— claim 1 , —C(═NR)— claim 1 , —SO— claim 1 , —P(═O)(OR)— claim 1 , optionally substituted heterocyclyl claim 1 , optionally substituted aryl claim 1 , —[O—(C-Calkylene)]- claim 1 , —[NHR—(C-Calkylene)] claim 1 , —[S—(C-Calkylene)]- claim 1 , and combinations thereof; wherein Ris H or optionally substituted C- ...

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21-11-2013 дата публикации

RESIN COMPOSITE MATERIAL AND PROCESS FOR PRODUCING SAME

Номер: US20130310521A1
Принадлежит:

Disclosed herein are a resin composite material that has excellent mechanical strength and can be easily produced and a method for producing such a resin composite material. 1. A resin composite material obtained by chemically bonding a reactive polyfunctional compound to both a thermoplastic resin and a carbon material having a graphene structure.2. The resin composite material according to claim 1 , wherein the reactive polyfunctional compound has reactive functional groups claim 1 , and wherein the reactive functional groups are functional groups selected from the group consisting of a carboxyl group claim 1 , a carbonyl group claim 1 , a sulfonic acid group claim 1 , a hydroxyl group claim 1 , an isocyanate group claim 1 , a silyl group claim 1 , a siloxy group claim 1 , an alkoxy group claim 1 , a vinyl group claim 1 , chlorine claim 1 , an aryl group claim 1 , an amino group claim 1 , an ether group claim 1 , an ester group claim 1 , an amide group claim 1 , a thiol group claim 1 , a (meth)acryl group claim 1 , and an epoxy group.4. The resin composite material according to claim 3 , wherein the compound having a structure represented by the formula (1) or the compound in which the compounds having a structure represented by the formula (1) are chemically bonded together is the compound having a structure represented by the formula (1).5. The resin composite material according to claim 3 , wherein the compound having a structure represented by the formula (1) or the compound in which the compounds having a structure represented by the formula (1) are chemically bonded together is a compound B in which the compounds having a structure represented by the formula (1) are bonded together claim 3 , and wherein in the compound B claim 3 , a moiety derived from at least one of the compounds having a structure represented by the formula (1) is chemically bonded to the thermoplastic resin and at least one of moieties derived from the other compounds having a structure ...

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26-12-2013 дата публикации

NOVEL INITIATION PROCESS FOR POLYMERIZATION WITH ACTIVATION USING IONIC LIQUIDS

Номер: US20130345380A1
Принадлежит: EVONIK DEGUSSA GmbH

The present invention relates to an innovative polymerization technique for (meth)acrylates and styrenes, in which the polymerization is initiated by isocyanates and special bases with imine structure and is activated/accelerated by addition of ionic liquids. With this new technique, which can be employed selectively, it is also possible to produce high molecular weight poly(meth)acrylates with in some cases narrow molecular weight distribution. 1. A method for initiating polymerization , comprising initiatingpolymerization of a vinylic monomer M with a component B and a component C,wherein the component B is an organic base,and the component C is an ionic liquid.2. The method of claim 1 , whereinthe initiating further comprises adding a component A, which is an isocyanate or a carbodiimide, additionally to the mixture, andcomponent A and component B are added separately from one another to the monomer M.3. The method of claim 2 , wherein the initiating comprises adding component B to a mixture of component A claim 2 , the ionic liquid C claim 2 , and a vinylic monomer M.4. The method of claim 2 , wherein the initiating comprises adding component A to a mixture of component B claim 2 , the ionic liquid C claim 2 , and a vinylic monomer M.5. The method of claim 1 , wherein the initiating is performed at a temperature below 50° C.6. The method of claim 2 , wherein the component A is dodecyl isocyanate claim 2 , ethyl isocyanate claim 2 , 1 claim 2 ,6-hexa-methylene diisocyanate (HDI) claim 2 , an HDI trimer claim 2 , cyclohexyl isocyanate claim 2 , tert-butyl isocyanate claim 2 , phenyl isocyanate claim 2 , toluene diisocyanate (TDI) claim 2 , isophorone diisocyanate (IPDI) claim 2 , or an IPDI trimer.7. The method of claim 1 , wherein the component C is a substance which is liquid below 100° C. and is composed of a cation and an anion.8. The method of claim 7 , wherein the cation is an imidazolium claim 7 , a pyridinium claim 7 , a pyrrolidinium claim 7 , a ...

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14-01-2021 дата публикации

Thermoplastic acrylic resin and method for producing same, and resin composition

Номер: US20210009802A1
Принадлежит: Kaneka Corp

A thermoplastic acrylic resin is provided. The thermoplastic acrylic resin is a graft copolymer in which a stem polymer is an acrylic resin containing acrylonitrile and another ethylenically unsaturated monomer, and a branch polymer is a polymer composed of an ethylenically unsaturated monomer. The acrylonitrile is contained in an amount of 35 mass % or more and 84.5 mass % or less, the other ethylenically unsaturated monomer is contained in an amount of 15 mass % or more and 64.5 mass % or less, and the polymer composed of an ethylenically unsaturated monomer is contained in an amount of 0.5 mass % or more and 40 mass % or less. Thus, provided are a thermoplastic acrylic resin having improved melt-processability without compromising heat resistance, a method for producing the thermoplastic acrylic resin, a thermoplastic acrylic resin composition, a molded body, an acrylic fiber, and a method for producing the acrylic fiber.

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15-01-2015 дата публикации

POSITIVE RESIST COMPOSITION AND PATTERNING PROCESS

Номер: US20150017586A1
Принадлежит: SHIN-ETSU CHEMICAL CO., LTD.

A positive resist composition is provided comprising a polymer comprising recurring units having a carboxyl or phenolic hydroxyl group substituted with an acid labile group and recurring units of hydroxyanthraquinone or hydroxy-2,3-dihydro-1,4-anthracenedione methacrylate, and having a Mw of 1,000-500,000. The resist composition has a satisfactory effect of suppressing acid diffusion and a high resolution, and forms a pattern of good profile and minimal edge roughness after exposure. 3. The resist composition of wherein the polymer further comprises recurring units (c) having an adhesive group selected from the class consisting of hydroxyl claim 2 , carboxyl claim 2 , lactone ring claim 2 , carbonate claim 2 , thiocarbonate claim 2 , carbonyl claim 2 , cyclic acetal claim 2 , ether claim 2 , ester claim 2 , sulfonic acid ester claim 2 , cyano claim 2 , amide claim 2 , and —O—C(═O)-G- wherein G is sulfur or NH and c is a number in the range: 0 Подробнее

23-01-2020 дата публикации

Porous membrane, membrane module, water treatment device, and method for manufacturing porous membrane

Номер: US20200023322A1
Принадлежит: Mitsubishi Chemical Corp

Provided is a porous membrane that can be manufactured in uncomplicated steps, has high hydrophilicity and water permeability, and exhibits excellent anti-fouling properties when used in a membrane bioreactor method (MBR method). The porous membrane of the present invention is a porous membrane containing polymer (A) and polymer (B), wherein the polymer (A) is a membrane-forming polymer, the polymer (B) is a polymer having a unit (b1) represented by formula (1) and a unit (b2) based on hydroxyl group-containing (meth)acrylate, and the concentration (mass %) of the unit (b1) is equal to or higher than the concentration (mass %) of the unit (b2) in the porous membrane.

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24-04-2014 дата публикации

O-IMINO-ISO-UREA COMPOUNDS AND POLYMERIZABLE COMPOSITIONS THEREOF

Номер: US20140113987A1
Принадлежит: BASF SE

The invention relates to the use of O-imino-iso-urea compounds as source of radicals to polymerizable compositions comprising these O-imino-iso-urea and to new O-imino-iso-urea compounds. The O-Imino-isoureas compounds are compounds of the formula (I) 2. The compound of claim 1 , wherein n is 1.3. A composition claim 1 , comprising:an ethylenically unsaturated, polymerizable monomer or oligomer;{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'a compound of the formula I′ as defined in ; and'}optionally a photoinitiator.4. A process for preparing an oligomer claim 3 , a cooligomer claim 3 , a polymer or a copolymer claim 3 , comprising reacting the composition of under conditions of free radical polymerization.5. A coating process comprising:{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'applying a coating formulation comprising the compound of to a substrate; and'}polymerizing.6. A crosslinking process claim 1 , comprising heating a mixture comprising an unsaturated polymer resin and the compound of . This application is a divisional of U.S. application Ser. No. 13/319,244, filed on Jan. 13, 2012, which is a 35 U.S.C. §371 national stage patent application of international patent application PCT/EP10/056063, filed on May 5, 2010, the text of which is incorporated by reference, and claims foreign priority to EPO 09159664.3 filed on May 7, 2009 and EPO 09159604.9 filed on May 7, 2009, the entire content of which is incorporated herein by reference.The invention relates to the use of O-imino-iso-urea compounds as source of radicals in particular as polymerization initiators, to polymerizable compositions comprising these O-imino-iso-urea and to new O-imino-iso-urea compounds.Free-radical polymerization belongs to the most important polymerization methods. It is used for preparing many commercially important polymers such as polystyrene, PVC, polyacrylates, polymethacrylates, PAN and other polymers. For technical details, reference may be made to the still ...

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01-02-2018 дата публикации

METHOD OF FORMING THERMORESPONSIVE POLYMERS

Номер: US20180030171A1
Автор: Delgado Paula, Palkar Amit
Принадлежит: Phillips 66 Company

A method of forming a thermoresponsive polymer. The method proceeds by mixing 2-(3-(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)ureido)ethyl methacrylate and methacrylamide in the presence of a solvent form a monomer solution. An initiator is then added to the monomer solution to form a thermoresponsive polymer. 1. A method comprising:mixing 2-(3-(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)ureido)ethyl methacrylate and methacrylamide in the presence of an organic solvent to form a monomer solution;adding an initiator to the monomer solution to form a thermoresponsive polymer.2. The method of claim 1 , wherein the organic solvent is selected from the group consisting of: dimethyl sulfoxide claim 1 , dimethyl formamide claim 1 , ethyl acetate claim 1 , methanol claim 1 , dioxane claim 1 , tetrahydrofuran claim 1 , acetone claim 1 , methylene chloride and toluene and combinations thereof.3. The method of claim 1 , wherein monomer solution is heated to a temperature greater than 50° C.4. The method of claim 1 , wherein monomer solution is heated to a temperature greater than 70° C.5. The method of claim 1 , wherein the initiator is an addition-type initiator.6. The method of claim 1 , wherein the initiator is selected from the group consisting of: azo initiators claim 1 , azobisisobutyronitriles claim 1 , peroxides claim 1 , persulfates and combinations thereof.7. The method of claim 1 , wherein the mixing of monomer solution occurs at an elevated temperature.8. The method of claim 7 , wherein the elevated temperature is greater than 50° C.9. The method of claim 1 , wherein the thermoresponsive polymer is purified in a polar solvent.10. The method of claim 1 , wherein the thermoresponsive polymer is water soluble.12. The method of claim 1 , wherein the thermoresponsive polymer has an average molecular weight greater than 50 claim 1 ,000.11. A method comprising:mixing from about 0.01 mol % to about 50 mol % 2-(3-(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)ureido)ethyl ...

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01-02-2018 дата публикации

Method of forming thermoresponsive polymers

Номер: US20180030172A1
Автор: Amit Palkar, Paula Delgado
Принадлежит: Phillips 66 Co

A method of forming a thermoresponsive polymer. The method begins by mixing in the presence of an organic solvent to form a monomer solution. An initiator is then added to the monomer solution to form a thermoresponsive polymer. In this method, R1 and R4 can be independently selected from the group consisting of H and alkyl groups; R2 and R3 can be independently selected from the group consisting of H, alkyl, olefinic, aromatic, heterocyclic, halogen, ammonium, nitroxides, nitrates, nitrite amides, amines, esters, ethers, carboxylic acids, acyl chlorides, alcohols, nitriles, phosphates, phosphonates, sulfates, sulfonates, sulfide, sulfite, thiol, and combinations thereof; Y can be selected from the group consisting of O, N and S; R5 and R6 can be independently selected from the group consisting of alkyl, olefinic, heterocyclic, halogens, ammonium, carboxylic, amines, esters, amides and combinations thereof; and X are methylene groups from about 0 to about 20 carbons.

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01-02-2018 дата публикации

RESIN COMPOSITE, FILM, METHODS OF PRODUCING THE RESIN COMPOSITE AND THE FILM, MOLDED PRODUCT, AND ARTICLE

Номер: US20180030223A1
Принадлежит: KURARAY CO., LTD.

A resin composite, a method of producing the resin composite, a molded product, a film, and an article excellent in impact resistance are provided. The resin composite contains a methacrylic resin (A), which contains no less than 80% by mass of a structural unit derived from methyl methacrylate and has a melt viscosity η(A) of 1500 to 3500 Pa·s at 220° C. and a shear rate of 122/sec, and a triblock copolymer (B), which has a methacrylic acid ester polymer block (b2) coupled to each of two ends of an acrylic acid ester polymer block (b1), at a specific ratio. The triblock copolymer (B) includes the block (b1) and the block (b2) at a specific ratio and has a melt viscosity η(B) of 75 to 1500 Pa·s at 220° C. and a shear rate of 122/sec. The ratio of η(A)/η(B) is from 1 to 20. 1. A resin composite , comprising:65 to 99 parts by mass of a methacrylic resin (A) that comprises no less than 80% by mass of a structural unit derived from methyl methacrylate and that has a melt viscosity η(A) of 1500 to 3500 Pa·s at 220° C. and a shear rate of 122/sec; and1 to 35 parts by mass of a triblock copolymer (B) that comprises a methacrylic acid ester polymer block (b2) coupled to each of two ends of an acrylic acid ester polymer block (b1),whereinthe triblock copolymer (B) includes 30% to 60% by mass of the acrylic acid ester polymer block (b1) and 40% to 70% by mass of the methacrylic acid ester polymer block (b2),the triblock copolymer (B) has a melt viscosity η(B) of 75 to 1500 Pa·s at 220° C. and a shear rate of 122/sec, anda ratio η(A)/η(B) of the melt viscosity η(A) to the melt viscosity η(B) is from 1 to 20.2. The resin composite according to claim 1 , whereinthe methacrylic acid ester polymer blocks (b2) coupled to the respective ends of the acrylic acid ester polymer block (1) have different mass percentages relative to a total mass percentage of the triblock copolymer (B),(b2(H)) is the block with a higher mass percentage, and(b2(L)) is the block with a lower mass ...

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30-01-2020 дата публикации

FOAMED GEL TREATMENT FLUIDS AND METHODS OF USE

Номер: US20200032123A1
Принадлежит:

Certain foamed gel treatment fluids and methods of using the treatment fluids in wellbores penetrating subterranean formations are provided. In one embodiment, the treatment fluids comprise: an aqueous base fluid, a gas, a plurality of particulates, and a plurality of swellable particles each comprising a material having a first monomer, a second monomer, and a third monomer comprising a foamable surfactant. In one embodiment, the methods comprise: preparing a treatment fluid comprising an aqueous base fluid and a swellable particle that comprises a material having a first monomer, a second monomer, and a third monomer comprising a foamable surfactant; blending the treatment fluid with a gas to form a foamed gel; and introducing the foamed gel into a wellbore penetrating at least a portion of a subterranean formation. 1. A method comprising:preparing a treatment fluid comprising an aqueous base fluid and a swellable particle that comprises a material having a first monomer, a second monomer, and a third monomer comprising a foamable surfactant;blending the treatment fluid with a gas to form a foamed gel; andintroducing the foamed gel into a wellbore penetrating at least a portion of a subterranean formation.2. The method of wherein the second monomer comprises a pH-responsive moiety.3. The method of further comprising adding an acid to the treatment fluid.6. The method of further comprising contacting at least a portion of the foamed gel with a breaker.7. The method of wherein the breaker is selected from the group consisting of: an oxidizing agent claim 6 , an enzyme acid claim 6 , a catalyst of iron claim 6 , a catalyst of copper claim 6 , a catalyst of silver claim 6 , a base claim 6 , and any combination thereof.8. The method of wherein the treatment fluid further comprises a plurality of particulates claim 1 , and wherein at least a portion of the plurality of particulates is suspended in the foamed gel after blending the treatment fluid.9. The method of ...

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04-02-2021 дата публикации

SOLUTION FOR USE IN FILLING MICROMETER-SIZE CAVITIES

Номер: US20210032533A1

Solution for use in filling micrometer-size cavities (), the solution comprising a first solvent, a first polymer () having a first molecular weight, a second polymer () having a second molecular weight, luminophores () and a surfactant, the second molecular weight being 10 to 50 times greater than the first molecular weight. 1. A solution , comprising a first solvent , a first polymer having a first molecular weight , a second polymer having a second molecular weight , luminophores and a surfactant , the second molecular weight being 10 to 50 times greater than the first molecular weight.2. The solution according to claim 1 , wherein the first molecular weight is approximately 20 times greater than the second molecular weight.3. The solution according to claim 1 , wherein the first polymer and the second polymer are chosen independently of each other from the group consisting of a poly(meth)acrylate claim 1 , a polysiloxane claim 1 , a polycarbonate claim 1 , a poly(ε-caprolactone) claim 1 , a polystyrene and copolymers thereof.4. The solution according to claim 1 , wherein the first polymer and/or the second polymer are homopolymers.5. The solution according to claim 1 , wherein the first polymer and the second polymer are of the same chemical nature.6. The solution according to claim 1 , wherein the first polymer and the second polymer are poly(methyl methacrylate).7. The solution according to claim 1 , wherein the solution comprises a second solvent claim 1 , the boiling point of which is at least 30° C. higher than the temperature of the first solvent.8. The solution according to claim 6 , wherein the first solvent is butanone and the second solvent is anisole.9. The solution according to claim 1 , wherein the luminophores are selected from the group consisting of phosphors and quantum dots.10. The solution according to claim 1 , the luminophores have a largest dimension less than 1 μm.11. The solution according to claim 1 , wherein the ratio solvent/dry matter ...

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24-02-2022 дата публикации

METHOD FOR PRODUCING ORGANIC COMPOUND

Номер: US20220056004A1
Принадлежит: M. TECHNIQUE CO., LTD.

Provided is a method for producing an organic compound, the method making it possible to ensure an adequate reaction time and obtain a targeted substance at a high yield even in an organic reaction that requires a relatively long time to complete the reaction. A method for producing an organic compound, wherein the method is characterized in that: a fluid processing apparatus F used in the production method is equipped with an upstream processing unit that processes a fluid to be processed between at least two processing surfaces and that relatively rotate, and a downstream processing unit disposed downstream of the upstream processing unit, the downstream processing unit being provided with a plurality of labyrinth seals that function to retain and stir the fluid to be processed that has been processed by the upstream processing unit; due to the fluid to be processed, which contains at least one type of organic compound, being passed through the upstream processing unit, the fluid to be processed is subjected to upstream processing; due to the fluid to be processed that has been subjected to upstream processing being passed through the downstream processing unit, the fluid to be processed that has been subjected to upstream processing is subjected to downstream processing; and the upstream processing and the downstream processing are performed continuously. 1. A method for producing an organic compound , whereina fluid processing apparatus used in the production method comprises an upstream-side processing part in which a fluid to be processed is processed between at least two processing surfaces that rotate relative to each other, and a downstream-side processing part is arranged in the downstream side of the upstream-side processing part and is provided with a plurality of labyrinth seals having functions of retaining and stirring the fluid to be processed being processed in the upstream-side processing part, whereinby the fluid to be processed which contains at ...

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18-02-2021 дата публикации

INTERMEDIATE FILM FOR LAMINATED GLASS AND LAMINATED GLASS

Номер: US20210046740A1
Принадлежит:

Provided is an interlayer film for laminated glass capable of enhancing the sound insulating property over a wide temperature range with width of at least 15° C. in a temperature region from 10° C. to 30° C. An interlayer film for laminated glass according to the present invention is an interlayer film for laminated glass having a two or more-layer structure, the interlayer film includes a layer containing a cured product or a polyolefin resin, the cured product is a cured product of a photocurable compound or a moisture-curable compound, the layer containing a cured product or a polyolefin resin has a glass transition temperature of −10° C. or more and 0° C. or less, tan δ at the glass transition temperature of the resin layer of 2.5 or more, and a storage modulus G′ at −5° C. of the resin layer of 3.0×10Pa or more and 5.0×10Pa or less. 1. An interlayer film for laminated glass having a two or more-layer structure ,the interlayer film comprising a resin layer,the resin layer having a glass transition temperature of −10° C. or more and 0° C. or less,the resin layer having tan δ at the glass transition temperature of 2.5 or more,{'sup': 4', '6, 'the resin layer having a storage modulus G′ at −5° C. of 3.0×10Pa or more and 5.0×10Pa or less.'}2. The interlayer film for laminated glass according to claim 1 , whereinthe resin layer is a layer containing a cured product or a polyolefin resin, andthe cured product is a cured product of a photocurable compound or a moisture-curable compound.3. The interlayer film for laminated glass according to claim 2 , wherein the cured product is a cured product of a photocurable compound.4. An interlayer film for laminated glass having a two or more-layer structure claim 2 ,the interlayer film comprising a resin layer,the resin layer being a layer containing a cured product or a polyolefin resin,the cured product being a cured product of a curable compound having a (meth)acryloyl group,{'sup': 4', '6, 'the layer containing cured ...

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19-02-2015 дата публикации

CONTINUOUS POLYMERIZATION APPARATUS AND PROCESS FOR PRODUCING POLYMER COMPOSITION

Номер: US20150051359A1
Принадлежит: Sumitomo Chemical Company, Limited

Continuous polymerization apparatus including a first reactor of a complete mixing type and a second reactor of a complete mixing type (). Each of the reactors () is provided with a supply port (), an effluent port (), and a temperature detecting means (T) for detecting a temperature in the reactor, wherein the supply port () of the first reactor () is connected to the supply sources () of a raw material monomer and a polymerization initiator, and the effluent port () of the first reactor is connected through a connection line () to the supply port () of the second reactor (). Connection line () is combined with a secondary line (′) for supplying a raw material monomer at a combining part (M) located between the effluent port () of the first reactor () and the supply port () of the second reactor (). 1. A continuous polymerization apparatus which comprises , at least , a first reactor and a second reactor which are of a complete mixing type ,wherein each of the reactors is provided with a supply port, an effluent port, and a temperature detecting means for detecting a temperature in the reactor,the supply port of the first reactor is connected to supply sources of a raw material monomer and a polymerization initiator,the effluent port of the first reactor is connected through a connection line to the supply port of the second reactor,the connection line is combined with a secondary line for supplying a raw material monomer at a combining part located between the effluent port of the first reactor and the supply port of the second reactor, andwherein the secondary line is connected to a source of the raw material monomer, and at least one of said source and said secondary line is provided with a temperature regulating means.2. (canceled)3. The continuous polymerization apparatus according to claim 1 , wherein the connection line is provided with a cooling means.4. The continuous polymerization apparatus according to claim 1 , wherein the connection line is provided ...

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14-02-2019 дата публикации

PROCESS FOR THE PRODUCTION OF HIGH INTERNAL PHASE EMULSION FOAMS

Номер: US20190048111A1
Принадлежит:

A method for polymerizing an open-cell foam including exposing an emulsion comprising a photoinitiator to an Ultraviolet light source, partially polymerizing the top surface of the emulsion, and moving the partially polymerized emulsion to a second polymerization stage. 19.-. (canceled)1024.-. (canceled)25. A method for polymerizing an open-cell foam comprising:exposing a High Internal Phase Emulsion comprising a free-radical initiator to an Ultraviolet light source; andpartially polymerizing the top surface of the High Internal Phase Emulsion.26. The method of claim 25 , wherein the High Internal Phase Emulsion is moved to a curing oven.27. The method of claim 25 , wherein the High Internal Phase Emulsion is moved to a multi-tiered curing oven.28. The method of claim 25 , wherein the High Internal Phase Emulsion further comprises an oil phase a monomer claim 25 , a cross-linking agent claim 25 , an emulsifier and an aqueous phase.29. The method of claim 25 , wherein the UV light is in the wavelength range of from about 200 nm to about 800 nm.30. The method of claim 25 , wherein the source of UV light is a UV lamp.31. The method of claim 25 , wherein the High Internal Phase Emulsion is exposed to the UV light for less than about 1 minute.32. The method of claim 25 , wherein the free-radical initiator is at least one of ammonium persulfate claim 25 , sodium persulfate claim 25 , potassium persulfate claim 25 , 2 claim 25 ,2′-azobis(N claim 25 ,N′-dimethyleneisobutyramidine)dihydrochloride claim 25 , persulfate-bisulfate and persulfate-ascorbic acid.33. The method of wherein the curing oven is a multi-tiered curing oven comprising at least three curing oven belts.34. The method of wherein the top surface has a z-stick measurement of less than 0.70N.35. The method of claim 25 , wherein an aqueous phase and an oil phase of the High Internal Phase Emulsion are combined in a ratio between about 8:1 and about 140:1.36. The method of claim 25 , wherein the High Internal ...

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25-02-2021 дата публикации

Resin composition, and prepreg, resin-coated film, resin-coated metal foil, metal-clad laminate, and wiring board each obtained using said resin composition

Номер: US20210054197A1

One aspect of the present invention relates to a resin composition containing (A) a thermosetting compound having a styrene structure or a (meth)acrylate structure, and (B) at least one of maleimide compounds represented by the formulas (1) to (3).

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08-05-2014 дата публикации

ON-DEMAND PHOTOINITIATED POLYMERIZATION

Номер: US20140128494A1
Принадлежит: California Institute of Technology

Compositions and methods for adjustable lenses are provided. In some embodiments, the lenses contain a lens matrix material, a masking compound, and a prepolymer. The lens matrix material provides structure to the lens. The masking compound is capable of blocking polymerization or crosslinking of the prepolymer, until photoisomerization of the compound is triggered, and the compound is converted from a first isomer to a second isomer having a different absorption profile. The prepolymer is a composition that can undergo a polymerization or crosslinking reaction upon photoinitiation to alter one or more of the properties of the lenses. 1. A composition comprising:(a) a masking compound capable of photoisomerization between a first isomer and a second isomer upon absorption of electromagnetic energy at a first wavelength and intensity; and(b) a prepolymer capable of polymerization upon photoinitiation with electromagnetic energy at a second wavelength and intensity.2. The composition of claim 2 , wherein the first isomer of the masking compound absorbs more light at the second wavelength than does the the second isomer of the masking compound.3. The composition of claim 1 , wherein the prepolymer comprises a photocrosslinker or a photoinitiator.4. The composition of claim 3 , wherein the photocrosslinker or photoinitiator has an absorption maximum that is about 50 nm or less from the absorption maximum of the first isomer of the masking compound.5. The composition of claim 1 , wherein the composition is an intraocular implant further comprising a matrix material.6. The composition of claim 1 , wherein the masking compound is described by the structure of formula (I):{'br': None, 'sup': 1', '2, 'sub': n1', 'n2, '(Z)—Y—(Z)\u2003\u2003(I)'}wherein Y is a photoisomerizable moiety;{'sup': 1', '2, 'nand nare each independently 0, 1, 2 or 3; and'}{'sup': 1', '2, 'each Zand Zis independently a polymerizable moiety or a crosslinking moiety that is connected to Y via an ...

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10-03-2022 дата публикации

Method for Controlled Release Using Mechanical Force

Номер: US20220073534A1
Принадлежит: California Institute of Technology

A general and modular mechanophore platform that efficiently releases a cargo molecule via a mechanically triggered cascade reaction is described, along with methods of synthesis and use thereof. The mechanophore platform comprises a stable Diels-Alder adduct mechanophore comprising a 2-furylcarbinol derivative as its diene component, wherein the 2-furylcarbinol derivative is, in turn, pre-loaded with a covalently attached cargo molecule, and wherein the Diels-Alder adduct mechanophore is embedded into a polymer chain or polymer network, such that the mechanophore platform undergoes the retro [4+2] cycloaddition reaction under mechanical force to reveal the unstable2-furylcarbinol derivative, which, in turn, easily decomposes under mild conditions to release its molecule cargo. 2. The mechanophore platform of claim 1 , wherein the furan comprises at least one substituent at a position of the 2-furylcarbinol scaffold selected from a group consisting of: α-position claim 1 , 3-position claim 1 , 4-position claim 1 , 5-position claim 1 , and any combination thereof.3. The mechanophore platform of claim 2 , wherein the at least one substituent is an electron-donating functional group.4. The mechanophore platform of claim 2 , wherein the at least one substituent is at at least one position selected from a group consisting of: 3-position claim 2 , 4-position claim 2 , 5-position claim 2 , α-position claim 2 , and any combination thereof; and wherein the at least one substituent is claim 2 , each claim 2 , independently selected from a group consisting of: alkyl claim 2 , alkenyl claim 2 , aryl claim 2 , heteroaryl claim 2 , any other aromatic or heteroaromatic functional group claim 2 , alkoxy claim 2 , aryloxy claim 2 , amine claim 2 , sulfide claim 2 , any other heteroatom-containing group claim 2 , including silane claim 2 , a polymer chain of any composition claim 2 , and any combination thereof.5. The mechanophore platform of claim 2 , wherein the at least one ...

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07-03-2019 дата публикации

ACRYLATE COATING COMPOSITIONS COMPRISING A UV LIGHT CLEAVABLE CROSS-LINKING AGENT

Номер: US20190071574A1
Принадлежит:

The present disclosure provides a coating composition for forming a coating that at least partially mobilizes in response to UV light, the composition comprising a monomer selected from acrylates, methacrylates and mixtures thereof, a cross-linking agent comprising two sub-units covalently bonded together, each sub-unit comprising an unsaturated group which is co-polymerisable with the monomer, wherein the two sub-units are adapted to dissociate in response to irradiation by UV light. The cross-linking agent may be present in the coating composition in an amount of less than 15 mol % of the total of the monomer and cross-linking agent. 1. A coating composition for forming a coating that at least partially mobilises in response to UV light , the composition comprising:a monomer selected from the group consisting of acrylates, methacrylates and mixtures thereof,a cross-linking agent comprising two sub-units covalently bonded together, each sub-unit comprising an unsaturated group which is co-polymerisable with the monomer,wherein the two sub-units are adapted to dissociate in response to irradiation by UV light, andwherein the cross-linking agent is present in the coating composition in an amount of less than about 15 mol % of the total of the monomer and cross-linking agent.2. The coating composition according to claim 1 , wherein the two sub-units are adapted to dissociate by a cycloelimination reaction in response to irradiation by UV light.3. The coating composition according to claim 1 , wherein the cross-linking agent is a [2π+π2] cycloaddition dimer or a [4π+π4] cycloaddition dimer of the two sub-units.4. The coating composition according to claim 3 , wherein the cross-linking agent comprises a dimer of coumarin claim 3 , thymine claim 3 , stilbene claim 3 , cinnamic acid claim 3 , anthracene claim 3 , or derivatives or combinations thereof.5. The coating composition according to claim 1 , wherein the unsaturated group is selected from the group consisting of ...

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05-03-2020 дата публикации

Air void control composition for bulk monomer polymerization

Номер: US20200071431A1
Принадлежит: Arkema France SA

The invention relates to the use of low levels of aliphatic short-chain saturated esters to control air void formation in any exothermic polymerization reaction in which the exotherm exceeds the boiling point of the monomer. One such polymerization is the bulk polymerization of one or more monomers having carboxylic acid ester monomers, at a level of at least 10% of total monomer. The aliphatic short-chain saturated esters are used in the polymerization mixture at levels of 0.5 to 10 weight percent, based on the carboxyl-containing monomer. The invention is especially useful in polymerization of methylmethacrylate polymers and copolymers, either neat, or as a polymer composite system.

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05-03-2020 дата публикации

ADHESIVES AND METHODS OF MAKING THE SAME

Номер: US20200071576A1
Принадлежит: PURDUE RESEARCH FOUNDATION

Embodiments of this invention relate to adhesives, and more particularly to biomimetic heteropolymer adhesive compositions. Certain embodiments relate to biomimetic terpolymer adhesive compositions including dopamine methacrylamide, 3,4-dihydroxyphenylalanine, or 3,4-dihydroxy styrene, mimicking moieties found in marine mussel adhesive proteins. In some embodiments, elastic moduli of the adhesives are preferably selected to match the elastic moduli of the substrates to minimize stress concentrations, to increase the ductility of the adhesive-substrate system, or both. 1. An adhesive composition comprising a heteropolymer including one of dopamine methacrylamide or 3 ,4-dihydroxyphenylalanine or 3 ,4-dihydroxystyrene , andat least one of methyl methacrylate, styrene, and poly(ethylene glycol) methyl ether methacrylate.2. The adhesive composition of claim 1 , wherein the one of dopamine methacrylamide or 3 claim 1 ,4-dihydroxyphenylalanine or 3 claim 1 ,4-dihydroxystyrene is present in a proportion of about 10% to about 50% by mole percentage.3. The adhesive composition of claim 2 , wherein the one of dopamine methacrylamide or 3 claim 2 ,4-dihydroxyphenylalanine or 3 claim 2 ,4-dihydroxystyrene is present in a proportion of about 20% to about 40% by mole percentage.4. The adhesive composition of claim 3 , wherein the one of dopamine methacrylamide or 3 claim 3 ,4-dihydroxyphenylalanine or 3 claim 3 ,4-dihydroxystyrene is present in a proportion of about 28% to about 36% by mole percentage.5. The adhesive composition of claim 1 , wherein the heteropolymer is a terpolymer includingof dopamine methacrylamide or 3,4-dihydroxyphenylalanine or 3 dihydroxystyrene;methyl methacrylate or styrene; andpoly(ethylene glycol) methyl ether methacrylate.6. The adhesive composition of claim 1 , wherein the heteropolymer includes dopamine methacrylamide and at least one of methyl methacrylate and poly(ethylene glycol) methyl ether methacrylate.7. The adhesive composition of claim 1 , ...

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24-03-2016 дата публикации

Cyanostilbenes

Номер: US20160083655A1
Принадлежит: ROLIC AG

The present invention relates to novel compounds that are particularly useful for the alignment, especially photoalignment, of slave material, especially liquid crystals for optical or electro-optical applications, such as security applications, liquid crystal devices or optical or electro-optical films.

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26-03-2015 дата публикации

LIGANDS DESIGNED TO PROVIDE HIGHLY ACTIVE CATALYST COMPLEXES

Номер: US20150087795A1
Принадлежит:

A series of ligands with site specific electron donating substituents that form a catalyst complex with a transition metal and are suitable for catalysis of atom transfer radical reactions, including ATRP are described. Faster catalysis rates were observed allowing for low catalyst concentrations and linear increases in molecular weight with monomer conversion, and narrow molecular weight distributions. Cyclic voltammetry revealed that increasing the strength and number of conjugated electron donating groups resulted in more stable complexes and larger ATRP equilibrium constants. 1. A catalyst complex for a redox-based atom transfer radical addition reaction , an atom transfer radical coupling reaction or a controlled radical polymerization reaction , the catalyst comprising:a transition metal; anda ligand comprising from 2 to 6 heteroatom containing groups capable of bonding to or chelating with a transition metal, wherein at least one of the heteroatom containing groups comprises a structure selected from an aromatic ring comprising an anionic heteroatomic donor substituent or a nitrogen containing heteroaromatic ring, wherein the aromatic ring or heteroaromatic ring further comprises one or more electron donating substituents,wherein the ligand forms a ligand/metal catalyst complex with the transition metal.2. The catalyst complex according to claim 1 , wherein the one or more electron donating substituents are located on a ring atom that is meta- or para- to the anionic heteroatomic donor substituent or the nitrogen of the heteroaromatic ring.3. The catalyst complex according to claim 1 , wherein the anionic heteroatomic donor substituent is selected from —O claim 1 , —S claim 1 , —CO claim 1 , —SO claim 1 , and —NR″ claim 1 , where R″ is —H or (C-C)alkyl.4. The catalyst complex according to claim 1 , wherein the one or more electron donating substituents are independently selected from straight chain (C-C)alkyl claim 1 , branched (C-C)alkyl claim 1 , —NR claim ...

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31-03-2022 дата публикации

Composition

Номер: US20220098344A1
Принадлежит: Sumitomo Chemical Co Ltd

Provided is a molded body having excellent heat resistance. A composition containing methyl methacrylate, methyl isobutyrate and methyl acrylate, in which a content of methyl methacrylate is 99.5% by mass or more, a concentration of methyl isobutyrate is 20 ppm by mass to 300 ppm by mass, and a concentration of methyl acrylate is 5 ppm by mass to 200 ppm by mass.

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29-03-2018 дата публикации

RAFT AGENT, POLYMERIZATION METHOD, POLYMER, RUBBER MIXTURE, AND USE THEREOF

Номер: US20180086865A1
Принадлежит:

Disclosed are RAFT agents, a method of polymerizing alkenes, dienes, vinyl compounds, and/or vinylidene compounds using at least one RAFT agent, polymers prepared by the methods, sulfur-crosslinkable rubber mixtures prepared by the methods, and motor vehicle tires, cords, belts, or hoses incorporating the sulfur-crosslinkable rubber mixtures. In one embodiment, the RAFT agent has the formula Z—C(═S)—S—R—S—P or P—S—Z—C(═S)—S—R—S—P, wherein P is a protecting group, and Z and R are typical RAFT Z and R groups. 1. A RAFT agent of formula I):{'br': None, 'Z—C(═S)—S—R—S—P,\u2003\u2003I)'}whereinZ is a Z group typical of RAFT polymerization,R is an R group typical of RAFT polymerization,C is a carbon atom,S is a sulfur atom,{'sub': 2', '2, 'sup': 2', '3', '4', '5', '6', '7', '8', '9, 'P is a protecting group selected from the group consisting of: S(═O)—R, S—C(═S)—N—RR, C(═O)—R, N—RR, SiRRR, and S(═O)—OM,'}{'sup': '1', 'R=alkyl, benzyl, or phenyl,'}{'sup': 2', '3, 'Rand R=alkyl, benzyl, or phenyl,'}{'sup': '4', 'R=alkyl,'}{'sup': '5', 'R=hydrogen atom (H), alkyl, benzyl, or phenyl,'}{'sup': '6', 'R=alkyl, benzyl, or phenyl,'}{'sup': 7', '8', '9, 'R, Rand R=alkyl or benzyl, and'}M=Na, K, or H.4. The RAFT agent of claim 1 , a) phenyl,', 'b) phenoxy,', 'c) alkoxy (O-alkyl) having 1 to 30 carbon atoms, wherein the alkyl is branched or unbranched,', 'd) alkyl having 1 to 30 carbon atoms, wherein the alkyl is branched or unbranched,', 'e) S-alkyl having 1 to 30 carbon atoms, wherein attachment to the —C(═S)—S—R—S—P radical of the RAFT agent is via the sulfur atom, and wherein the alkyl is branched or unbranched,', 'f) a heterocyclic group,', 'g) alkyl(phenyl)amino, wherein alkyl is 1 to 30 carbon atoms, wherein attachment to the —C(═S)—S—R—S—P radical of the RAFT agent is via the nitrogen atom, and wherein the alkyl is branched or unbranched, and', 'h) dialkylamino, wherein alkyl is 1 to 30 carbon atoms, wherein each alkyl is independently branched or unbranched, wherein ...

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02-04-2015 дата публикации

Nanostructures from Laser-Ablated Nanohole Templates

Номер: US20150093550A1
Принадлежит:

Solution casting a nanostructure. Preparing a template by ablating nanoholes in a substrate using single-femtosecond laser machining. Replicating the nanoholes by applying a solution of a polymer and a solvent into the template. After the solvent has substantially dissipated, removing the replica from the substrate. 116-. (canceled)17. A nanostructure , comprising:(a) a polymer, and(b) an aspect ratio of at least ten-to-one,wherein said nanostructure is prepared from a nanohole formed within a transparent substrate by ablation using a single femtosecond laser pulse.18. The nanostructure of claim 17 , wherein said aspect ratio exceeds twenty-five-to-one.19. The nanostructure of claim 17 , wherein said nanostructure comprises a length greater than ten microns and a width less than one micron.20. The nanostructure of claim 19 , wherein said nanostructure comprises a length of at least thirty microns and a width less than one micron.21. The nanostructure of claim 17 , wherein said nanostructure is cast claim 17 , synthesized claim 17 , molded claim 17 , replicated claim 17 , imprinted claim 17 , or embossed from said nanohole.22. The nanostructure of claim 17 , further comprising an array of nanostructures claim 17 , each having an aspect ratio of at least ten-to-one claim 17 , said array being fabricated from a plurality of nanoholes claim 17 , each formed within a transparent substrate by ablation using a single femtosecond laser pulse.23. The nanostructure of claim 22 , wherein said nanostructures are non-randomly positioned.24. A method for fabricating a nanostructure claim 22 , comprising:(a) providing a template of transparent material;(b) ablating at least one nanohole in said template using a single femtosecond laser pulse;(c) filling said at least one nanohole with a first polymeric material; and(d) extracting said first polymeric material as the nanostructure,wherein said nanostructure has an aspect ratio of at least ten-to-one.25. The method of claim 24 , ...

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19-03-2020 дата публикации

ACTIVE ENERGY RAY CURABLE COMPOSITION, STEREOSCOPIC MODELING MATERIAL, ACTIVE ENERGY RAY CURABLE INK, INKJET INK, ACTIVE ENERGY RAY CURABLE COMPOSITION CONTAINER, TWO-DIMENSIONAL OR THREE-DIMENSIONAL IMAGE FORMING APPARATUS, TWO-DIMENSIONAL OR THREE-DIMENSIONAL IMAGE FORMING METHOD, CURED PRODUCT, AND PROCESSED PRODUCT

Номер: US20200087535A1
Принадлежит:

An active energy ray curable composition including a polymerization initiator and a polymerizable compound is provided. When the active energy ray curable composition is formed into a cured film on a substrate under the specific condition, the cured film satisfies the following conditions (1) and (2): 117-. (canceled)18. An active energy ray curable composition , comprising:a polymerization initiator;a polymerizable compound; anda black pigment,wherein the polymerizable compound comprises at least one monofunctional monomer and at least one polyfunctional monomer and/or polyfunctional oligomer,wherein the polymerization initiator includes at least two members selected from the group consisting of an aminoalkylphenone compound, an acylphosphine oxide compound, and a thioxanthone derivative,wherein the monofunctional monomer comprises at least one acrylamide compound selected from the group consisting of acryloyl morpholine and methacryloyl morpholine,{'sup': '2', 'wherein, when the active energy ray curable composition is formed into a film having an average thickness of 10 μm on a substrate and irradiated active energy ray until an accumulated amount of light becomes 300 mL/cmto become a cured film, the cured film satisfies the following conditions (1) and (2)(1) when the substrate is a polyethylene terephthalate substrate, the cured film on the substrate has a transmission density of from 1.5 to 3.0 that is measured with a transmission densitometer, and{'b': 1', '2', '2', '1, '(2) when the substrate is a polycarbonate substrate, the cured film on the substrate has a first length (L) and a second length (L) before and after a tensile test, respectively, and a ratio of the second length (L) to the first length (L) ranges from 1.5 to 4.0, wherein the tensile test includes forming the cured film on the substrate into a dumbbell-shaped specimen No. 6 defined in Japanese Industrial Standards K6251 and stretching the specimen with a tensile tester at a stretching speed of ...

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05-04-2018 дата публикации

CHEMICALLY PATTERNED GUIDE LAYERS FOR USE IN CHEMOEPITAXY DIRECTING OF BLOCK CO-POLYMERS

Номер: US20180096838A1
Автор: Dai Jinhua, Lowes Joyce
Принадлежит:

The present invention is broadly concerned with materials, processes, and structures that allow an underlayer to be imaged directly using conventional lithography, thus avoiding the photoresist processing steps required by prior art directed self-assembly (DSA) processes. The underlayers can be tailored to favor a selected block of the DSA block co-polymers (BCP), depending on the pattern, and can be formulated either to initially be neutral to the BCP and switch to non-neutral after photoexposure, or can initially be non-neutral to the BCP and switch to neutral after exposure. These materials allow fast crosslinking to achieve solvent resistance and possess good thermal stability. 2. The method of claim 1 , wherein said initial surface property comprises an initial surface energy and the altered surface property comprises an altered surface energy that is different from said initial surface energy.3. The method of claim 2 , wherein:the dispersive and polar components of said initial surface energy are from about 33 dyne/cm to about 41 dyne/cm and from about 3 dyne/com to about 10 dyne/cm, respectively; andthe dispersive and polar components of said altered surface energy are from about 25 dyne/cm to about 36 dyne/cm and from about 8 dyne/cm to about 13 dyne/cm, respectively.4. The method of claim 1 , wherein:said initial surface property is a lack of affinity towards one of said first and second blocks over the other of said first and second blocks; andduring said exposing, an affinity to one of said first and second blocks over the other of said first and second blocks develops, said affinity being the altered surface property.5. The method of claim 4 , wherein said affinity is towards the first block claim 4 , and during said causing the first block assembles and forms said first self-assembled region at said altered surface property.6. The method of claim 4 , wherein said patternable layer comprises a polymer dispersed or dissolved in a solvent system claim 4 , ...

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08-04-2021 дата публикации

Column packing material for supercritical fluid chromatography, column for supercritical fluid chromatography and preparation method therefor

Номер: US20210101131A1
Принадлежит: Shimadzu Corp

A column packing material for supercritical fluid chromatography which allows good peak shape to be obtained in the analysis of free fatty acids, etc. and in the analysis of agricultural chemicals, etc., and has excellent durability for repeated analysis. The column packing material for supercritical fluid chromatography includes polymer particles containing cross-linked polymer, the degree of swelling of which after absorbing tetrahydrofuran and the degree of swelling of which after absorbing methanol are both 1.4 or less.

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21-04-2016 дата публикации

Substrate for flexible display device and flexible display device

Номер: US20160108152A1

A substrate for a flexible display device according to an embodiment of the present invention may include a self-supporting film where a particle has a grafted polymer chain and is disposed in two dimensions or three dimensions through the grafted polymer chain.

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11-04-2019 дата публикации

ACRYLIC POLYMER COMPOSITION

Номер: US20190106552A1
Принадлежит: ZEON CORPORATION

Provided is an acrylic polymer composition comprising an acrylic polymer and a polyfunctional organic compound represented by the following general formula (1): 3. The acrylic polymer composition according to claim 1 , wherein k is 6.4. The acrylic polymer composition according to claim 1 , wherein the polyfunctional organic compound has a half-life of 5 hours or longer at 190° C.5. The acrylic polymer composition according to claim 1 , wherein a content ratio of the polyfunctional organic compound is an amount of 0.002 or more in terms of the number of equivalents of a urea group contained in the polyfunctional organic compound with respect to an ester group contained in the acrylic polymer.6. The acrylic polymer composition according to claim 1 , wherein a content ratio of the polyfunctional organic compound is 0.4 parts by weight or more in terms of a weight ratio per 100 parts by weight of the acrylic polymer.7. A cross-linked product prepared by cross-linking an acrylic polymer composition according to . The disclosure relates to an acrylic polymer composition, and in particular, relates to an acrylic polymer composition effectively prevented from being thermally degraded under heating.With developments in petrochemistry, polymers constituted by organic compounds have contributed in various forms such as plastics, rubbers, fibers, and films to the evolution of humans. These polymers are used in various environments according to purposes and as such, have each been improved such that they can be used for a long period by imparting durability thereto in expected environments. For example, plastics for outdoor use have been developed as products provided with ultraviolet-resistant performance, and rubbers functioning even in severe cold areas have been developed as products provided with cold-resistant performance.Meanwhile, internal combustions typified by engines, which have been used in increased amounts with industrial developments, require lubricating oils ...

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10-07-2014 дата публикации

PHOTOCURABLE ELASTOMER COMPOSITIONS

Номер: US20140193652A1
Принадлежит: Henkel Corporation

The present invention relates to photocurable elastomer compositions and methods of preparation and use of such compositions for cure-in-place applications such as gaskets. The curable compositions generally include an elastomer component, a monofunctional and/or multifunctional reactant and a photoinitiator that in various aspects may be a visible and/or UV curing initiator. The various components may be present in different amounts, depending on the combination of components and composition desired. 1. A composition comprising:{'sub': 1', '10, 'a) about 35 to about 65 weight percent of an elastomer comprising alkyl (meth)acrylate polymers selected from the group consisting of homopolymers of C-Calkyl (meth)acrylates;'}b) about 1.0 to about 25 weight percent of a multiftmnctional reactant; andc) about 0.1 to about 10.0 weight percent of a photoinitiator.2. The composition of claim 1 , wherein said muitifunctional reactant comprises a (meth)acrylic crosslinking agent.3. The composition of claim 2 , wherein said (meth)acrylic crosslinking agent is selected from the group consisting of: ethylene glycol diacrylate; ethylene glycol dimethacrylate; 1 claim 2 ,6-hexanediol diacrylate; 1 claim 2 ,6-hexanedioi dimethacrylate; 1 claim 2 ,4-butanedioi diacrylate; pentaerythritol triacrylate; pentaerythritoi tetraacryiate; dipentaerythritol pentaacryiate claim 2 , methoxy-1 claim 2 ,6-hexanedioipentaerythritol triacrylate; trimethylolpropane triacrylate; tetraethyiene glycol diacrylate; polymethacrylate urethanes; epoxy acrylates; polyester acrylate monomers and oligomers; trimethyloipropane propoxylate triacrylate; poly-n-butyleneoxide glycol diacrylates; bisphenol A alkylene oxide adduct diacrylates; and mixtures thereof.4. The composition of claim 1 , wherein said photoinitiator is selected from the group consisting of: benzophenone; substituted benzophenones; acetophenone; substituted acetophenones; benzoin; benzoin alkyl esters; xanthone; substituted xanthones; phosphine ...

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26-04-2018 дата публикации

Maleinated Derivatives

Номер: US20180111912A1
Принадлежит: ELEVANCE RENEWABLE SCIENCES, INC.

This invention relates to malienated derivatives made from maleic anhydride, functionalized monomers, and one or more additional reagents, e.g., an oxygen-containing reagent (e.g., alcohol, polyol), a nitrogen-containing reagent (e.g., amine, polyamine, aminoalcohol), a metal and/or a metal compound. The invention relates to lubricants, functional fluids, fuels, dispersants, detergents and functional compositions (e.g., cleaning solutions, food compositions, etc.) 176-. (canceled)77. A maleinated derivative composition comprising: a functionalized polymer , wherein the functionalized polymer is reacted with maleic anhydride on one or more carbon-carbon double bonds of the functionalized polymer to form a maleinated functionalized polymer;wherein the functionalized polymer is formed via olefin metathesis from one or more functionalized monomers; andwherein the one or more functionalized monomers are unsaturated fatty acid glycerides.78. The maleinated derivative of claim 77 , wherein the unsaturated fatty acid glycerides comprise unsaturated fatty acid monoglycerides claim 77 , unsaturated fatty acid diglycerides claim 77 , unsaturated fatty acid triglycerides claim 77 , or combinations of two or more of the foregoing.79. The maleinated derivative of claim 77 , wherein the unsaturated fatty acid glycerides are derived from a natural oil.80. The maleinated derivative of claim 79 , wherein the natural oil is a vegetable oil claim 79 , an algae oil claim 79 , a fungus oil claim 79 , an animal fat claim 79 , a tall oil claim 79 , or any combination of two or more of the foregoing.81. The maleinated derivative of claim 80 , wherein the natural oil is a vegetable oil.82. The maleinated derivative of claim 80 , wherein the natural oil is canola oil claim 80 , rapeseed oil claim 80 , coconut oil claim 80 , corn oil claim 80 , cottonseed oil claim 80 , olive oil claim 80 , palm oil claim 80 , peanut oil claim 80 , safflower oil claim 80 , sesame oil claim 80 , soybean oil ...

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30-04-2015 дата публикации

VINYL RESIN AND RESIN COMPOSITION

Номер: US20150119497A1
Принадлежит:

The present invention aims to provide a vinyl resin which, with a polyurethane resin, is capable of providing a film excellent in mechanical strength, weather resistance, solvent resistance, and water resistance. The vinyl resin (V1) of the present invention is obtainable by polymerizing monomer components including a monomer (X) represented by the formula (1): 3. The vinyl resin according to claim 1 ,wherein the aromatic polycarboxylic acid having 3 or more carboxyl groups in the formula (1) has a structure wherein carboxyl groups bond to the 2 carbon atoms adjacent to a carbon atom which has no substituent among the carbon atoms constituting the aromatic ring, anda carboxyl group bonds to at least one of the carbon atoms which are adjacent to the 2 carbon atoms having the carboxyl groups and which are different from the carbon atom that has no substituent.4. The vinyl resin according to claim 1 ,wherein the aromatic polycarboxylic acid having 3 or more carboxyl groups in the formula (1) is trimellitic acid and/or pyromellitic acid.5. The vinyl resin according to claim 1 ,wherein a is 1 and c is 1 in the formula (1).6. The vinyl resin according to claim 1 ,wherein the monomer (X) has a hydroxy value of 0 to 500 mgKOH/g.7. The vinyl resin according to claim 1 ,wherein the monomer (X) has an L concentration of 0.5 to 10 mmol/g.8. The vinyl resin according to claim 1 ,wherein the monomer (X) has a carbonyl concentration of 1.5 to 30 mmol/g.9. The vinyl resin according to claim 1 ,wherein the vinyl resin (V1) has a number average molecular weight (Mn) of 5,000 to 1,000,000.10. The vinyl resin according to claim 1 ,wherein the vinyl resin (V1) has a glass transition temperature of −50° C. to 80° C.11. The vinyl resin according to claim 1 ,wherein the vinyl resin (V1) comprises at least one reactive group selected from the group consisting of silanol, alkoxysilyl, epoxy, carboxyl, hydroxy, primary or secondary amino, isocyanato, blocked isocyanato, vinyl, oxazoline, ...

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07-05-2015 дата публикации

Polymerization using latent initiators

Номер: US20150126696A1
Принадлежит: Evonik Industries AG

The present invention relates to a novel, rapid initiation mechanism for polymerising (meth)acrylates using latent initiators based on N-heterocyclic carbene compounds which can be thermally activated, such as, in particular, N-heterocyclic carbene-CO 2 compounds, carbene-CS 2 compounds or carbene-metal compounds (NHC). Using the new initiation mechanism, molecular weights of 10 000 to over 500 000 g/mol and a narrow polydispersity can be achieved for polymerisation of MMA. The polymerisations can be carried out both without solvent and in solution.

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04-05-2017 дата публикации

Acrylic rubber, acrylic rubber composition, cross-linked acrylic rubber product, and seal member

Номер: US20170121439A1
Принадлежит: Honda Motor Co Ltd, Zeon Corp

An acrylic rubber contains (a) methyl methacrylate units, (b) ethyl acrylate units, (c) n-butyl acrylate units, (d) 2-methoxyethyl acrylate units, and (e) cross-linking site monomer units, in which the acrylic rubber contains 10 to 20% by weight of (a) the methyl methacrylate units, 15% by weight or less of (b) the ethyl acrylate units, 60 to 80% by weight of (c) the n-butyl acrylate units, 10 to 30% by weight of (d) the 2-methoxyethyl acrylate units, and 0.5 to 5% by weight of (e) the cross-linking site monomer units.

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25-04-2019 дата публикации

Lubricant and srt material

Номер: US20190119596A1

The invention provides an SRT material (lubricant) applicable to machine elements such as bearings, seals or guides (guiding mechanisms) that constitute a slide part of a machine. A lubricant and an SRT material are disclosed.

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10-05-2018 дата публикации

BIJELS AND METHODS OF MAKING THE SAME

Номер: US20180127577A1

A method of making a bijel includes dispersing surface-active nanoparticles in a ternary liquid mixture. The ternary liquid mixture includes a hydrophilic liquid, a hydrophobic liquid, and a solvent. The ternary liquid mixture is contacted with water. A bijel includes a stable mixture of two immiscible liquids separated by an interfacial layer of colloidal particles. The bijel has temperature-independent stability, and the domain sizes are below one micrometer. 1. A method of making a bijel comprising:dispersing surface-active nanoparticles in a ternary liquid mixture, wherein the ternary liquid mixture comprises a hydrophilic liquid, a hydrophobic liquid, and a solvent; andcontacting the ternary liquid mixture with water.2. The method of claim 1 , wherein the dispersing step is conducted in the presence of one or more surfactants.3. The method of claim 1 , wherein the hydrophobic liquid comprises at least one of diethyl phthalate claim 1 , dimethylphthalate claim 1 , 1 claim 1 ,6-hexanediol diacrylate claim 1 , 1 claim 1 ,6-diacetoxyhexane claim 1 , trimethylolpropane triacrylate claim 1 , dipentaerythritol pentaacrylate claim 1 , triacetin claim 1 , toluene claim 1 , chloroform claim 1 , laurylacrylate claim 1 , butylacrylate claim 1 , decanol claim 1 , styrene claim 1 , and oleic acid.4. The method of claim 1 , wherein at least one of the hydrophilic liquid and the hydrophobic liquid comprises a polymerizable monomer.5. The method of wherein the one or more surfactants and the nanoparticles are oppositely charged.6. The method of further comprising mixing the hydrophilic liquid claim 1 , the hydrophobic liquid and the solvent to form the ternary liquid mixture.7. The method of claim 1 , wherein the hydrophilic liquid comprises a liquid claim 1 , a polymerizable monomer claim 1 , or the combination of a liquid and a polymerizable monomer.8. The method of wherein the hydrophobic liquid comprises a liquid claim 1 , a polymerizable monomer claim 1 , or the ...

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10-05-2018 дата публикации

Process To Chemically Modify Polymeric Materials By Static, Low-Pressure Infiltration Of Reactive Gaseous Molecules

Номер: US20180127870A1
Принадлежит:

Disclosed herein are systems and methods for diffusing precursors into polymer substrates. 1. A method comprising:loading a substrate into a vacuum chamber of a chemical vapor infiltration reaction apparatus, the vacuum chamber having a first end and a second end with a high vacuum pump located proximate said second end;pumping the vacuum chamber to a pressure of from 8 mTorr to 12 mTorr with said vacuum pump;dosing the substrate with a precursor by allowing the precursor to flow inside the chamber;creating a static precursor atmosphere inside the chamber;allowing the substrate to rest in the static precursor atmosphere from 30 seconds to 1 day to form a chemically modified substrate; andextracting the chemically modified substrate from the vacuum chamber.2. The method of claim 1 , further comprising:extracting residual precursor from the chamber; andventing the vacuum chamber to atmospheric pressure.3. The method of claim 1 , wherein the substrate comprises an organic claim 1 , polymeric material.4. The method of claim 3 , wherein the organic claim 3 , polymeric material is selected from a group consisting of poly(methyl methacrylate) (PET) claim 3 , poly-(ethylene terephthalate) (PMMA) claim 3 , polycarbonate claim 3 , cellulose claim 3 , carboxylate-containing polymers claim 3 , and combinations thereof.5. The method of claim 4 , wherein the precursor comprises an inorganic material.6. The method of claim 5 , wherein the precursor comprises a vapor phase metalorganic precursor.7. The method of claim 6 , wherein the metalorganic precursor is selected from a group consisting of titanium tetrachloride claim 6 , zirconium tetrachloride claim 6 , zinc chloride claim 6 , aluminum trichloride claim 6 , silane claim 6 , tungsten hexafluoride claim 6 , molybdenum fluoride claim 6 , diethyl zinc claim 6 , tetraethylorthosilicate claim 6 , trim ethyl aluminum claim 6 , titanium isopropoxide claim 6 , dimethylchloro aluminum claim 6 , methyldichloro aluminum claim 6 , or ...

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11-05-2017 дата публикации

FUNCTIONALIZED QUINACRIDONE PIGMENTS

Номер: US20170130053A1
Автор: FEICK Jason D., Wu Ziyan
Принадлежит:

Quinacridone pigments that are surface-functionalized with glycidyl methacrylate, maleic anhydride, or 4-methacryloxyethyl trimellitic anhydride to create a functionalized pigment. The functional groups are then activated to bond hydrophobic polymers, thereby coating the pigment with the hydrophobic polymers. The quinacridone pigments can be used for a variety of applications. They are well-suited for use in electro-optic materials, such as electrophoretic media for use in electrophoretic displays. 2. The pigment of claim 1 , wherein the hydrophobic polymer is a polymer comprising lauryl acrylate claim 1 , lauryl methacrylate claim 1 , 2-ethylhexyl acrylate claim 1 , 2-ethythexyl methacrylate claim 1 , hexyl acrylate claim 1 , hexyl methacrylate claim 1 , n-octyl acrylate claim 1 , n-octyl methacrylate claim 1 , n-octadecyl acrylate claim 1 , n-octadecyl methacrylate claim 1 , or a combination thereof.6. The pigment of claim 1 , wherein Ris —H or Ris —CH.7. An electrophoretic medium comprising a pigment of .8. An electro-optic display comprising a pigment of .9. A front plane laminate comprising a pigment of .11. The method of claim 10 , wherein the pigment is dispersed in toluene and reacted with methacrylate claim 10 , maleic anhydride claim 10 , or 4-methacryloxyethyl trimellitic anhydride at a temperature greater than 40° C.12. The method of claim 10 , further comprising reacting the functionalized pigment with a hydrophobic polymer.13. The method of claim 12 , wherein the functionalized pigment and the hydrophobic polymer are ball milled together prior to reacting.14. The method of claims 12 , wherein the hydrophobic polymer is a polymer comprising lauryl acrylate claims 12 , lauryl methacrylate claims 12 , 2-ethylhexyl acrylate claims 12 , 2-ethylhexyl methacrylate claims 12 , hexyl acrylate claims 12 , hexyl methacrylate claims 12 , n-octyl acrylate claims 12 , n-octyl methacrylate claims 12 , n-octadecyl acrylate claims 12 , n-octadecyl methacrylate claims ...

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03-06-2021 дата публикации

ECO-FRIENDLY MATERIALS AND METHODS FOR RENEWABLE AND SUSTAINABLE APPLICATIONS IN MATERIAL CHEMISTRY

Номер: US20210163424A1
Принадлежит:

The invention relates to novel hydrazide-based templates, methods of making the same, and methods of using the hydrazide-based templates as molecular scaffolds for asymmetric light driven transformations, light driven material synthesis, and biological applications. Furthermore, the present invention relates to photoinitiators, monomers, and polymers derived from biomass, together with methods and methods of using the same. 1. A biomass derived , photodegradable polymer comprising at least one functionalized monomeric from the group consisting of: a phenacyl , a hydrazide , methylmethacrylate , or derivatives thereof.2. The photodegradable polymer of claim 1 , further comprising at least one second monomeric unit comprising a phototrigger.3. The photodegradable polymer of claim 2 , further comprising at least one third monomeric unit claim 2 , wherein the third monomeric unit is not a derived from biomass.4. The photodegradable polymer of claim 1 , wherein the first monomeric unit is also a photoinitiator.5. The photodegrabale polymer of claim 4 , wherein the photoinitiator is derived from biomass.6. The photodegradable polymer of claim 1 , wherein photocleavage of said polymer occurs from exposure to light from about 300 nm to about 450 nm in wavelength. This application is a divisional of U.S. patent application Ser. No. 16/124,418, filed Sep. 7, 2018, which is a continuation of PCT/US2017/21277, filed Mar. 8, 2017, which claims priority under 35 U.S.C § 119 to Provisional patent Application Ser. No. 62/305,044 filed Mar. 8, 2016, Provisional patent Application Ser. No. 62/324,194 filed Apr. 18, 2016, and Provisional patent Application Ser. No. 62/324,189 filed Apr. 18, 2016, herein incorporated by reference in their entirety.This invention was made with government support under Contract No. 1465075 awarded by the National Science Foundation (NSF), and by the National Science EPSCoR (EPS IIA-1355466) for the Center for Sustainable Materials Science (CSMS), North ...

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03-06-2021 дата публикации

FOAMED GEL TREATMENT FLUIDS AND METHODS OF USE

Номер: US20210163811A1
Принадлежит:

Certain foamed gel treatment fluids and methods of using the treatment fluids in wellbores penetrating subterranean formations are provided. In one embodiment, the treatment fluids comprise: an aqueous base fluid, a gas, a plurality of particulates, and a plurality of swellable particles each comprising a material having a first monomer, a second monomer, and a third monomer comprising a foamable surfactant. In one embodiment, the methods comprise: preparing a treatment fluid comprising an aqueous base fluid and a swellable particle that comprises a material having a first monomer, a second monomer, and a third monomer comprising a foamable surfactant; introducing the treatment fluid into a wellbore penetrating at least a portion of a subterranean formation; and blending the treatment fluid while in the wellbore to form a foamed gel. 1. A treatment fluid comprising: an aqueous base fluid , a gas , a plurality of particulates , and a plurality of swellable particles each comprising a material having a first monomer , a second monomer , and a third monomer comprising a foamable surfactant.2. The treatment fluid of wherein the treatment fluid is a foamed gel and wherein at least a portion of the plurality of particulates is suspended in the foamed gel.3. The treatment fluid of further comprising a surfactant selected from the group consisting of: a laureth sulfate claim 1 , a lauryl sulfate claim 1 , sodium cocoyl sarcosinate claim 1 , decyl polyglucose claim 1 , cocamidopropyl amine oxide claim 1 , lauramide DEA claim 1 , cocamidopropyl betaine (CAPB) claim 1 , sodium cocoamphoacetate (CAA) claim 1 , and any combination thereof.4. The treatment fluid of wherein the second monomer comprises a pH-responsive moiety.5. The treatment fluid of further comprising an acid.6. The treatment fluid of wherein the acid is glycolic acetic acid.7. The treatment fluid of wherein the third monomer is acrylic acid esterified with the foamable surfactant.8. The treatment fluid of ...

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03-06-2021 дата публикации

METHOD AND COMPOSITION FOR SELECTIVELY MODIFYING BASE MATERIAL SURFACE

Номер: US20210166935A1
Принадлежит: JSR Corporation

A composition for use in selective modification of a base material surface includes a polymer having, at an end of a main chain or a side chain thereof, a group including a first functional group capable of forming a bond with a metal, and a solvent. 1. A composition for use in selective modification of a base material surface , comprising:a polymer comprising, at an end of a main chain or a side chain thereof, a group comprising a first functional group capable of forming a bond with a metal; anda solvent.2. The composition according to claim 1 , wherein the metal is a constituent of a metal substance claim 1 , an alloy claim 1 , an oxide claim 1 , an electrically conductive nitride or a silicide.3. The composition according to claim 1 , wherein the metal is copper claim 1 , iron claim 1 , zinc claim 1 , cobalt claim 1 , aluminum claim 1 , titanium claim 1 , tin claim 1 , tungsten claim 1 , zirconium claim 1 , tantalum claim 1 , germanium claim 1 , molybdenum claim 1 , ruthenium claim 1 , gold claim 1 , silver claim 1 , platinum claim 1 , palladium or nickel.4. The composition according to claim 1 , wherein a polystyrene equivalent number average molecular weight of the polymer is no less than 500 and no greater than 50 claim 1 ,000.5. The composition according to claim 1 , wherein the first functional group is a cyano group claim 1 , a sulfanyl group claim 1 , an ethylenic carbon-carbon double bond-containing group claim 1 , an oxazoline ring-containing group claim 1 , a phosphoric acid group claim 1 , an epoxy group or a disulfide group.6. The composition according to claim 1 , wherein the polymer comprises a structural unit derived from substituted or unsubstituted styrene claim 1 , a structural unit derived from (meth)acrylic acid or a (meth)acrylic acid ester claim 1 , a structural unit derived from substituted or unsubstituted ethylene claim 1 , or a combination thereof.7. The composition according to claim 1 , wherein the polymer comprises claim 1 , at one ...

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18-05-2017 дата публикации

Surface modification methods for biomedical scaffolds

Номер: US20170137588A1

Many different substrates are used in tissue engineering as platforms to enhance cell attachment, proliferation and activity, either in-vitro, to multiply specific cell lines, or in-vivo, to induce shorter healing time of injured or missing tissue. However, their hydrophobicity and lack of specific functionalities make them non-ideal for cell adhesion and growth. Treating the surfaces by exposing them to a series of steps including, but not limited to, a diazonium based wet chemistry allows one or more functional groups to be applied to the surface improving cell adhesion and growth. Embodiments of the invention exploiting PDLLA, PMMA and roughed PEEK are demonstrated including both a one-stage and a two-stage process, and at times a vacuum treatment, allowing modification of inner and outer surfaces.

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18-05-2017 дата публикации

COLOR CONVERSION IN LCD DISPLAYS

Номер: US20170137627A1
Принадлежит:

Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and/or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. For example, rhodamine-based fluorescent compounds are used in matrices produced by sol gel processes and/or UV (ultraviolet) curing processes which are configured to stabilize the compounds and extend their lifetime—to provide the required emission specifications of the color conversion films. Film integration and display configurations further enhance the display performance with color conversion films utilizing various color conversion elements. 2. The color conversion film of claim 1 , produced at least partially by a sol gel process carried out using claim 1 , to provide a matrix for the at least one RBF compound claim 1 , a formulation comprising:an ESOR (epoxy silica ormosil) solution comprising TEOS (tetraethyl orthosilicate), at least one silane precursor, and GLYMO ((3-Glycidyloxypropyl) trimethoxysilane),a DURS (diurethane siloxane) powder comprising isocyanate-functionalized silica nanoparticles and ethylene glycol, anda transition metal alkoxide matrix solution.3. The color conversion film of claim 1 , further configured to shift some of a yellow region in the white illumination into a R transmission region of the R color filter.4. The color conversion film of claim 2 , wherein ratios (wt/vol/vol (mg/ml/ml)) of the DURS/the ESOR/and the transition metal alkoxide matrix solution are 15-25/1-3/1.5. The color conversion film of claim 2 , wherein the ESOR is prepared under acidic conditions.6. The color conversion film of claim 2 , wherein the at least one silane precursor comprises PhTMOS ( ...

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18-05-2017 дата публикации

COLOR CONVERSION IN LCD DISPLAYS

Номер: US20170137628A1
Принадлежит:

Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and/or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. For example, rhodamine-based fluorescent compounds are used in matrices produced by sol gel processes and/or UV (ultraviolet) curing processes which are configured to stabilize the compounds and extend their lifetime - to provide the required emission specifications of the color conversion films. Film integration and display configurations further enhance the display performance with color conversion films utilizing various color conversion elements. 2. The color conversion film of claim 1 , produced at least partially by a UV (ultraviolet) curing process carried out using claim 1 , to provide a matrix for the at least one RBF compound claim 1 , a formulation comprising 65-70% monomers claim 1 , 25-30% oligomers claim 1 , and 5% photointiator.3. The color conversion film of claim 2 , wherein:the monomers consist of at least one of: dipropylene glycol diacrylate, ditrimethylolpropane tetraacrylate, dipentaerythritol hexaacrylate, ethoxylated pentaerythritol tetraacrylate, propoxylated (3) glyceryl acrylate and trimethylolpropane triacrylate,the oligomers consist of at least one of: polyester acrylate, modified polyester resin diluted with dipropyleneglycol diacrylate and aliphatic urethane hexaacrylate, andthe photointiator consists of at least one of: alpha-hydroxy-cyclohexyl-phenyl-ketone and alpha-hydroxy ketone.4. The color conversion film of claim 2 , wherein 0.005-0.05% of the at least one RBF compound is added to the formulation.5. The color conversion film of claim 1 , further configured to shift ...

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14-08-2014 дата публикации

POROUS POLYMER STRUCTURES AND METHODS AND ARTICLES RELATING THERETO

Номер: US20140228463A1
Принадлежит: UNIVERSITY OF SOUTHERN CALIFORNIA

A porous polymer structure may be formed by cooling a substrate to a temperature at or below a freezing point of a monomer, wherein the monomer is capable of free-radical polymerization; exposing the substrate to an initiator and the monomer, each in a vapor phase, wherein a concentration of the monomer in the vapor phase is above a saturation pressure of the monomer; converting the initiator to a free radical; crystalizing and depositing the monomer on the substrate; and polymerizing at least some of the monomer on the substrate, thereby forming a porous polymer structure on the substrate. 1. A method comprising:cooling a substrate to a temperature at or below a freezing point of a monomer, wherein the monomer is capable of free-radical polymerization;exposing the substrate to an initiator and the monomer, each in a vapor phase, wherein a concentration of the monomer in the vapor phase is above a saturation pressure of the monomer;converting the initiator to a free radical;crystalizing and depositing the monomer on the substrate; andpolymerizing at least some of the monomer on the substrate, thereby forming a porous polymer structure on the substrate.2. The method of claim 1 , wherein the porous polymer structure comprises microstructures that comprise a polymer claim 1 , wherein the polymer is a polymerization product of reactants that comprise the free radical and the monomer.3. The method of claim 2 , wherein the porous polymer structure has two types of pores: (1) intracrystalline pores within microstructures and (2) intercrystalline pores between the microstructures.4. The method of claim 3 , wherein a pore size of at least some of the intracrystalline pores is about 10 nm to about 10 microns.5. The method of claim 3 , wherein a pore size of at least some of the intercrystalline pores is about 1 micron to about 500 microns.6. The method of further comprising:removing the porous polymer structure from the substrate.7. The method of further comprising:after ...

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10-06-2021 дата публикации

SEPARATOR FOR SECONDARY BATTERY AND LITHIUM SECONDARY BATTERY INCLUDING SAME

Номер: US20210175584A1
Принадлежит: LG CHEM, LTD.

The present invention relates to a separator for a secondary battery, the separator including a substrate and a coating layer formed on the surface of the substrate, wherein the coating layer includes an organic binder and inorganic particles, and the organic binder contains an ethylenically unsaturated group, and to a lithium secondary battery including the same. 2. The separator of claim 1 , wherein the ethylenically unsaturated group is at least one selected from the group consisting of a vinyl group claim 1 , an acryloxy group and a methacryloxy group.4. The separator of claim 1 , wherein the organic binder is included in an amount of 1 part by weight to 80 parts by weight based on 100 parts by weight of the coating layer.5. A lithium secondary battery comprising:a positive electrode;a negative electrode;{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'the separator of ; and'}a gel polymer electrolyte disposed between the positive electrode and the negative electrode and the separator, comprising a polymer of an oligomer containing a (meth) acrylate group,wherein the separator comprises a polymer network in a three-dimensional structure of a polymer of the organic binder containing an ethylenically unsaturated group and the oligomer containing a (meth) acrylate group.6. The secondary battery of claim 5 , wherein the oligomer further contains an oxyalkylene group.7. The secondary battery of claim 5 , wherein the oligomer is represented by Formula 1 below:{'br': None, 'sub': '1', 'A-C-A′\u2003\u2003[Formula 1]'}{'sub': '1', 'wherein, in Formula 1, A and A′ are each independently a unit containing a (meth) acrylate group, and Cis a unit containing an oxyalkylene group.'}11. The secondary battery of claim 5 , wherein the gel polymer electrolyte is formed by injecting a gel polymer electrolyte composition including the oligomer into a battery case and then curing the composition. This application claims the benefit of Korean Patent Application No. 10-2018-0006795, ...

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15-09-2022 дата публикации

POLYMERIZATION PROCESS WITH A BORANE-AMINE COMPLEX

Номер: US20220289873A1
Принадлежит:

The invention relates to a process for polymerizing at least one radically polymerizable compound having at least one ethylenic bond in the presence of a borane complex BH3 with an amine as a radical initiator, said process comprising the steps of: providing a borane complex BH3 with an amine; and bringing the complex into contact with a composition comprising at least one radically polymerizable compound having at least one ethylenic bond; wherein the polymerization is performed in the absence of an oxidizing agent and/or an additional radical initiator other than the borane complex BH3 with an amine. The invention also relates to a composition comprising at least one radically polymerizable compound having at least one ethylenic bond and a borane complex BH3 with an amine, wherein the composition is free of an oxidizing agent and/or an additional radical initiator other than the borane complex BH3 with an amine, as well as the use of said composition as an adhesive for bonding two substrates together. 115-. (canceled)18. The process as claimed in claim 16 , wherein the radically polymerizable compound is selected from the group consisting of a styrene claim 16 , vinyl claim 16 , acrylic claim 16 , and methacrylic monomer claim 16 , and combinations thereof.19. The process as claimed in claim 16 , wherein the complex of borane BHwith an amine is present at a content by mass of 0.01% to 25% claim 16 , relative to the mass of the radically polymerizable compound.20. The process as claimed in claim 16 , wherein the radically polymerizable compound has a content by mass of 5% to 100% claim 16 , relative to the total mass of the composition.21. The process as claimed in claim 16 , comprising a heating step after bringing the complex into contact with the composition comprising at least one polymerizable compound.22. The process as claimed in claim 21 , wherein the heating step is carried out at a temperature of 20 to 100° C.23. The process as claimed in claim 16 , ...

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31-05-2018 дата публикации

Method for producing photocured three-dimensional stereoscopic shaped object

Номер: US20180147776A1
Автор: Jun Kotani
Принадлежит: Kaneka Corp

A process for producing a photocured three-dimensional stereoscopic shaped object includes ejecting and applying a droplet of a photocurable resin composition (A) having a viscosity of 20 mPa·s to 500 Pa·s at 23° C. using a non-contact dispenser, wherein the droplet has a volume of 1 nL or more.

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11-06-2015 дата публикации

Vacuum forming process and use

Номер: US20150158237A1
Принадлежит: Evonik Industries AG

A vacuum thermoforming process for producing a transparent molding free from optical defects, whereby the prior temperature of the mold and preform is controlled, the preform is premolded, the mold is shaped under sub-atmospheric pressure, the mold shape is cooled, and the transparent molding is removed. The transparent plastic molding is produced from polymethyl methacrylate (PMMA) or polycarbonate (PC) with particularly good optical quality and with relatively low cycle times. Upon removal, these moldings are dimensionally stable, free from distortion, and exhibit no surface defects such as pimples.

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18-06-2015 дата публикации

NOVEL POLYMERIC PHOTOINITIATORS AND PHOTOINITIATOR MONOMERS

Номер: US20150166716A1
Принадлежит:

The present invention provides polymeric photoinitiators being co-polymers of photoinitiator monomers and at least one further monomer, as well as the photoinitiator monomers being intermediates in the preparation of such polymeric photoinitiators. Additionally there is provided polyacrylate obtained by radical polymerization of at least one acrylate monomer (Ac) in the presence of such polymeric photoinitiators. In the photoinitiator monomers and polymeric photoinitiators, a photoinitiator moiety and a tertiary amine are incorporated into the photoinitiator structure. 150-. (canceled)52. The polymeric photoinitiator according to claim 51 , wherein Z is selected from an optionally substituted —O—(C-Calkylene)- claim 51 , an optionally substituted —S—(C-Calkylene)- claim 51 , and an optionally substituted —NR—(C-Calkylene)-.53. The polymeric photoinitiator according to claim 51 , wherein Ris an optionally substituted C-Calkyl.54. The polymeric photoinitiator according to claim 51 , wherein Wand Weach independently are selected from —CHOH claim 51 , —OH claim 51 , —NH claim 51 , —NHR claim 51 , and —SH.55. The polymeric photoinitiator according to claim 51 , wherein Wand Ware the same.56. The polymeric photoinitiator according to claim 51 , wherein Xand Xare independently selected from a single bond or an optionally substituted C-Calkylene.57. The polymeric photoinitiator according to claim 51 , wherein Xand Xare the same.58. The polymeric photoinitiator according to claim 51 , wherein Pi is a photoinitiator moiety selected from the group consisting of benzoin ethers claim 51 , phenyl hydroxyalkyl ketones claim 51 , phenyl aminoalkyl ketones claim 51 , benzophenones claim 51 , thioxanthones claim 51 , xanthones claim 51 , acridones claim 51 , anthraquinones claim 51 , fluorenones claim 51 , dibenzosuberones claim 51 , benzils claim 51 , benzil ketals claim 51 , α-dialkoxy-acetophenones claim 51 , α-hydroxy-alkyl-phenones claim 51 , α-amino-alkyl-phenones claim 51 , ...

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28-08-2014 дата публикации

Thickening vinyl copolymers

Номер: US20140243479A1
Принадлежит: Conopco Inc

A rheology modifier copolymer of formula (I) wherein A is a macromonomer, B is an acrylic or methacrylic acid or salt thereof, C is a C 1 -C 8 ester of (meth)acrylic acid, D is an associative monomer, and when present E is a crosslinking monomer.

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24-06-2021 дата публикации

PROCESS FOR PREPARING AN ULTRA-HIGH MOLECULAR WEIGHT POLYMER VIA EMULSION POLYMERIZATION AT ROOM TEMPERATURE

Номер: US20210189047A1
Принадлежит:

A process for preparing an ultra-high molecular weight polymer via emulsion polymerization at the room/indoor temperature includes using persulfate as initiator, water as medium, anionic surfactant as emulsifier, sodium bicarbonate as pH regulator, styrene, (meth) acrylate or vinyl acetate as monomer, which is subjected to a free radical polymerization at room temperature and the normal pressure. The ultra-high molecular weight polymers may have weight average molecular weights larger than 1,000,000 g/mol. The monomer conversion may be above 85% after reacting for 1˜6 hours. The process may be carried out at room temperature and normal pressure without the addition of other assist initiators. There temperature and pressure of the reaction may not be controlled, and the molecular weight and molecular weight distribution may be adjusted and controlled in a wider range. 1. A process for preparing an ultra-high molecular weight polymer via emulsion polymerization at room temperature comprising: a persulfate as an initiator , water as a medium , an anionic surfactant as an emulsifier , sodium bicarbonate as a pH regulator , styrene , vinyl acetate or (meth) acrylate as a monomer to polymerize by free radical emulsion; to obtain the ultra-high molecular weight polymer wherein the weight average molecular weight of the ultra-high molecular weight polymer is larger than 1 ,000 ,000 g/mol;wherein the initiator is potassium persulfate or ammonium persulfate; the molar ratio of the initiator and the monomer is 1-5:100;wherein the surfactant is sodium dodecyl benzene sulfonate or sodium dodecyl sulfate;wherein the mass ratio of the water and the monomer is 2-5:1;wherein the mass ratio of the surfactant and the monomer is 4-6:100 and the mass ratio of the pH modifier sodium bicarbonate and the monomer is 2-4:100;wherein the pH value is adjusted to 7-8 for stability of the process;wherein the room temperature is between 25° and 35° C.; andwherein the polymerization reaction time ...

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16-06-2016 дата публикации

Photocrosslinkable block copolymers for hot-melt adhesives

Номер: US20160168298A1
Принадлежит: Henkel AG and Co KGaA, Henkel Corp

Disclosed is a method for formation of block copolymers using a Single Electron Transfer Living Radical Polymerization (SET-LRP) process. The process can be used to form di and tri-block copolymers from vinyl monomers. In one embodiment the SET-LRP process comprises initially forming a macroinitiator using SET-LRP to form a first block of a di or tri-block copolymer and then using SET-LRP to form additional blocks of the copolymer. The produced block copolymers have very narrow polydispersity indexes and controlled molecular weights. The process permits incorporation of photoinitiators in any of the block formation reactions. The method also includes purification processes that result in a block copolymer having very low color making it useful in a variety of applications. In one application block copolymers prepared according to the present process can be used in hot-melt adhesives.

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25-06-2015 дата публикации

SILICONE (METH)ACRYLATE PARTICLES, PROCESSES FOR THEIR PREPARATION AND USE THEREOF

Номер: US20150175724A1
Принадлежит: Evonik Industries AG

Particles obtainable by polymerization of a siloxane which has at least one (meth)acrylate group of the formula (I) 1. A process for producing silicone (meth)acrylate particles , said process comprising: [{'br': None, 'sub': '2', '—O—C(O)—CR═CH\u2003\u2003(I)'}, {'sub': '3', 'where R=—H or —CH,'}, 'with the addition of at least one solid-body emulsifier and mixing of the two phases, where the organic phase forms an inner phase of the emulsion, and, 'a) producing an emulsion of an aqueous phase and an organic phase, wherein the organic phase has at least one radical initiator and at least one siloxane having at least one (meth)acrylate group of formula (I)'}b) fully polymerizing the inner phase of the emulsion in the presence of a radical initiator which is more soluble in the organic phase than in the aqueous phase, wherein the at least one siloxane has an average molar ratio of groups of formula (I) to Si atoms of less than 0.1.3. The process according to claim 1 , wherein the radical initiator is added in a concentration of 0.05 to 2% by weight claim 1 , based on the inner phase of the emulsion.4. The process according to claim 1 , wherein the solid-body emulsifier has an average particle size dof >100 nm to 200 nm.5. The process according to claim 1 , wherein the solid-body emulsifiers are selected from metal oxides claim 1 , mixed oxides claim 1 , nitrides claim 1 , hydroxides claim 1 , carbonates and silicates which are at least (partially)hydrophobicized with at least one compound selected from the group consisting of silanes claim 1 , siloxanes claim 1 , quaternary ammonium compounds claim 1 , cationic polymers and fatty acids or anions thereof.7. The process according to claim 6 , wherein the radical is selected formulae (Ib) and (Ie).8. The process according to claim 2 , wherein the variable a is from 50 to 220.9. The process according to claim 2 , wherein the variable c is a value from 4 to 12 claim 2 , or c=0 and all of the radicals Rare those radicals ...

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23-06-2016 дата публикации

Dental material including propylbarbituric acid polymerization catalyst

Номер: US20160175203A1
Принадлежит: Shofu Inc

The present invention relates to a polymerization catalyst having storage stability under an oral cavity environment. Furthermore, the present invention relates to a dental material cured by use of the present polymerization catalyst. The polymerization catalyst for use in the dental material is achieved with including 1-cyclohexyl-5-propylbarbituric acid and trioctylmethylammonium chloride.

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06-06-2019 дата публикации

Composition for the Manufacture of an Ophthalmic Lens Comprising an Encapsulated Light-Absorbing Additive

Номер: US20190169438A1
Принадлежит:

The present invention relates to a thermosetting composition for the manufacture of an ophthalmic lens which efficiently absorbs light rays without degradation of the light-absorbing additive, said composition comprising an allyl monomer or oligomer, a catalyst, at least one light-absorbing additive contained in nanoparticles which are dispersed in said allyl monomer or allyl oligomer. The present invention also relates to the use of said composition and to the ophthalmic lens obtained from said composition. 1. A polymerizable liquid composition for the manufacture of an ophthalmic lens , comprising:a) at least one allyl monomer or allyl oligomer,b) at least one catalyst for initiating the polymerization of said allyl monomer or allyl oligomer,c) at least one light-absorbing additive contained in nanoparticles which are dispersed in said allyl monomer or allyl oligomer.2. The composition according to claim 1 , wherein the light-absorbing additive is selected from the group consisting of a colorant; a colorless light-absorbing additive; and mixtures thereof.3. The composition according to claim 1 , wherein the nanoparticles comprise a polymer.4. The composition according to claim 1 , wherein nanoparticles comprise a mineral oxide.5. The composition according to claim 1 , wherein the refractive index of the nanoparticles is from 1.47 to 1.56 claim 1 , as measured according to the ISO 489:1999.6. The composition according to claim 1 , wherein the nanoparticles exhibit a size of from 1 nm to 10 μm claim 1 , as measured according to the Dynamic Light Scattering method.7. The composition according to claim 1 , wherein the amount of light-absorbing additive in the nanoparticles is from 0.0001 to 90 wt % based on the weight of the nanoparticles.8. The composition according to claim 1 , wherein the amount of nanoparticles in the composition is from 0.01 to 2 wt % based on the weight of the composition.9. The composition according to claim 1 , wherein the allyl monomer or ...

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18-09-2014 дата публикации

Methods and apparatus for controlled single electron transfer living radical polymerization

Номер: US20140275448A1
Принадлежит: Henkel Corp

This invention provides methods for controlled single electron transfer living radical polymerization (SET-LRP) of monomers with increased conversion, high molecular weights and low polydispersity by allowing the polymerization to proceed at low temperatures via a tubular reactor either made of copper or containing copper metal surface.

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15-07-2021 дата публикации

METHACRYLIC RESIN, SHAPED ARTICLE, AND OPTICAL COMPONENT OR AUTOMOTIVE PART

Номер: US20210214477A1
Принадлежит: ASAHI KASEI KABUSHIKI KAISHA

A methacrylic resin having a cyclic structure in a main chain thereof, a shaped article, and an optical component or automotive part, in which the glass transition temperature is higher than 120° C. and 160° C. or lower, and the sign of the orientational birefringence when being oriented so as to have a degree of orientation of 0.03 is different from the sign of the orientational birefringence when being oriented so as to have a degree of orientation of 0.08. 1. A methacrylic resin ,the methacrylic resin having a cyclic structure in a main chain thereof,the methacrylic resin having a glass transition temperature of higher than 120° C. and 160° C. or lower,wherein a sign of an orientational birefringence when being oriented so as to have a degree of orientation of 0.03 is different from the sign of the orientational birefringence when being oriented so as to have a degree of orientation of 0.08.2. The methacrylic resin according to claim 1 , wherein{'sup': −5', '−5, 'an absolute value of the orientational birefringence when being oriented so as to have a degree of orientation of 0.03 is 0.1×10or more and 5.0×10or less, and'}{'sup': '−5', 'the absolute value of the orientational birefringence when being oriented so as to have a degree of orientation of 0.08 is 8.0×10or less.'}3. The methacrylic resin according to claim 2 , wherein{'sup': −5', '−5, 'the absolute value of the orientational birefringence when being oriented so as to have a degree of orientation of 0.03 is 0.1×10or more and 3.0×10or less, and'}{'sup': '−5', 'the absolute value of the orientational birefringence when being oriented so as to have a degree of orientation of 0.08 is 5.0×10or less.'}4. A methacrylic resin claim 2 ,the methacrylic resin having a structural unit having a cyclic structure in the main chain thereof,the methacrylic resin having a glass transition temperature of higher than 120° C. and 160° C. or lower,wherein a difference in an abundance ratio of the structural unit having the ...

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07-07-2016 дата публикации

DEGRADABLE POLYMER RESINS AND METHODS FOR THEIR PREPARATION

Номер: US20160194417A1
Принадлежит: EMPIRE TECHNOLOGY DEVELOPMENT LLC

Disclosed are polymers having one or more two-photon absorbing chromophores in a backbone of the polymers. The polymers degrade upon two-photon excitation, which allows for easy decomposition of polymeric products made therefrom. The decomposition can occur when the polymer is exposed to light of intensities sufficient to induce the two-photon excitation, which in turn cleaves the polymer at one or more sites where the chromophores are attached. 1. A polymer resin having a polymeric backbone , the polymer resin comprising a first repeating unit and a second repeating unit , wherein the first repeating unit has a two-photon absorbing chromophore in the polymeric backbone.4. The resin of claim 1 , wherein the first repeating unit is present in the polymer resin in an amount of not more than about 2% by weight.5. The resin of claim 1 , wherein the second repeating unit comprises —(CH)n-O— claim 1 , —CH(Me)-CH—O— claim 1 , —CH—CH(OH)—CH—O— claim 1 , —CH(CHOH)—CH—O— claim 1 , —CH—C(Me)-CH—O— claim 1 , —CH—C(CHOH)—CH—O— claim 1 , or a combination thereof claim 1 , wherein n=2-6.6. The resin of claim 1 , wherein the second repeating unit comprises —C(═O)—Ar—C(═O)—CH—CH—O— claim 1 , —C(═O)—NH—Ar—CH—Ar—NH—C(═O)—O—CH—CH—O— claim 1 , —C(═O)—X—NH— claim 1 , or —C(═O)—X—O— claim 1 , wherein:{'sub': 3', '1', '6', '2', '2', '2, 'Xis —CH((C-C)alkyl)-, —(CH)n-, —Ar—C(═O)—NH—Ar—, or —(CH)n-C(═O)—NH—(CH)m-C(═O)—;'}Ar is 1,4-phenylene, 1,3-phenylene, or 1,2-phenylene;m=2, 3, 4, 5, or 6; andn=2, 3, 4, 5, or 6.7. The resin of claim 1 , wherein the resin further comprises a third repeating unit claim 1 , wherein the third repeating unit comprises —C(═NH)—Ar—C(═NH)—O— claim 1 , —C(═O)—Ar—C(═O)—O— claim 1 , —C(═O)—CH—CH—CH—CH—C(═O)—O— claim 1 , or a combination thereof claim 1 , whereinAr is 1,4-phenylene, 1,3-phenylene, or 1,2-phenylene.8. The resin of claim 1 , wherein the second repeating unit comprises —R—O—X—O—R—O— claim 1 , wherein:{'sup': '7', 'sub': 2', '2, 'Ris —CH—CHOH—CH—; and ...

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20-06-2019 дата публикации

Polyoxazoline-Containing Compositions Catalyzed with Onium Salt

Номер: US20190185700A1
Принадлежит: PPG Industries Ohio Inc

Polyoxazoline-containing compositions cured in the presence of an onium salt catalyst are disclosed.

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22-07-2021 дата публикации

METHOD FOR SYNTHESIZING MAGADIITE/PMMA NANO COMPOSITE MICROSPHERES BY USING PH VALUE REGULATION IN PICKERING EMULSION

Номер: US20210220793A1
Принадлежит: SOUTH CHINA UNIVERSITY OF TECHNOLOGY

The disclosure discloses a method for synthesizing magadiite/PMMA nano composite microspheres by using pH value regulation in a Pickering emulsion. According to the method, organic modified magadiite is used as an emulsifier, deionized water of which a pH value is regulated with a buffer solution is used as a solvent, and a methylmethacrylate monomer is used as an oil phase of a Pickering emulsion; stirring is performed to form the stable Pickering emulsion, and then a water-soluble free-radical initiator is added to initiate emulsion polymerization, thereby synthesizing magadiite/PMMA nano composite microspheres. 1. A method for synthesizing magadiite/PMMA nano composite microspheres by using pH value regulation in a Pickering emulsion , wherein the method comprises the following steps:step 1: adding a deionized water into a reaction container, adding a buffer solution to regulate a pH value, then adding an organic modified magadiite, and stirring and heating to 50° C. to 80° C., so that the organic modified magadiite is uniformly dispersed in the water;step 2: cooling to 30° C. to 40° C., adding a methylmethacrylate monomer, and continuously stirring to form a uniform and stable Pickering emulsion; andstep 3: heating the Pickering emulsion to 60° C. to 90° C., adding a water-soluble free-radical initiator, heating and keeping a temperature at 80° C. to 90° C., reacting for 3 hours to 5 hours, cooling to a temperature lower than 50° C., stopping stirring, drying in vacuum and grinding to obtain the magadiite/PMMA nano composite microspheres.2. The method according to claim 1 , wherein in the step 1 claim 1 , a mass of the deionized water accounts for 50 wt % to 90 wt % of a total mass of the Pickering emulsion.3. The method according to claim 1 , wherein in the step 1 claim 1 , the buffer solution is an HCl solution or a sodium bicarbonate solution.4. The method according to claim 1 , wherein in the step 1 claim 1 , the pH value is regulated between 3.0 and 11.0.5. ...

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14-07-2016 дата публикации

URAZOLE COMPOUNDS

Номер: US20160200707A1
Принадлежит: Universiteit Gent

The present invention relates to a compound of formula (I) or a stereoisomer, enantiomer, racemic, or tautomer thereof, (I) wherein R, R, R, R, R, R, R, Land Qhave the meaning defined in the claims and the description. The present invention also relates to a process for the preparation of the compound of formula (I). The present invention also relates to the use of a compound of formula (I) as an in situ precursor of a triazolinedione reagent for the functionalization of enes, dienes, aryl and heteroaryl systems via the ene reactions, Diels-Alder reactions, and electrophilic aromatic substitution reactions of said reagent. The present invention also relates to the use of a compound of formula (I) in polymers, membranes, adhesives, foams, sealants, molded articles, films, extruded articles, fibers, elastomers, polymer based additives, pharmaceutical and biomedical products, varnishes, paints, coatings, inks, composite material, organic LEDs, organic semiconductors, conducting organic polymers, or 3D printed articles. The present invention also relates to article comprising said compound of formula (I) and to a process for reshaping and/or repairing said article. 3. The compound according to claim 2 , wherein E is CRand m is 2.6. The compound according to claim 1 , wherein claim 1 ,{'sup': 1', '1, 'sub': 1-10', '1-10, 'Lis Calkylene; said Calkylene being unsubstituted or substituted with one or more Z;'}{'sup': 1', '14', '4', '15', '17', '1', '5, 'sub': q', 'q', 'p, 'claim-text': q is 1 or 2;', 'p is 0 or 1;', {'sup': 4', '2, 'sub': 1-6', '1-10, 'Lis a single bond or Calkylene; said Calkylene being unsubstituted or substituted with one or more Z;'}], 'Qis a single bond or is selected from the group consisting of —OC(O)—; —OC(O)—[CHR]—; and —OC(O)—[C(H)(L-O—R)]—[CHR]—O—; wherein each left side of said groups is attached to Land the right side thereof is attached to R; and wherein,'}{'sup': '1', 'sub': 2-10', '6-12', '6-12', '1-6', '6-12', '1-6', '6-12', '1-6, 'claim- ...

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12-07-2018 дата публикации

PROCESS FOR THE BIOLOGICAL PRODUCTION OF METHACRYLIC ACID AND DERIVATIVES THEREOF

Номер: US20180195095A1
Принадлежит:

A process of producing methacrylic acid and/or derivatives thereof including the following steps: (a) biologically converting isobutyryl-CoA into methacrylyl-CoA by the action of an oxidase; and (b) converting methacrylyl-CoA into methacrylic acid and/or derivatives thereof. The invention also extends to microorganisms adapted to conduct the steps of the process. 2. A microorganism modified by one or more heterologous nucleic acids to conduct the following steps:(a) biologically converting isobutyryl-CoA into methacrylyl-CoA by expression of an oxidase; and(b) biologically converting methacrylyl-CoA into methacrylic acid.3. A microorganism adapted to conduct the following steps:(a) biologically converting isobutyryl-CoA into methacrylyl-CoA by expression of an oxidase; and(b) biologically converting methacrylyl-CoA into methacrylic acid and/or derivatives thereof.4. The microorganism according to claim 3 , wherein the derivatives thereof of methacrylic acid are methacrylic acid esters.5. The microorganism according to claim 4 , wherein the microorganism expresses the following enzymes:an acyl-CoA oxidase; and one or more of:(i) an acyl-CoA thioesterase; (ii) a CoA transferase; (iii) an acid-thiol synthetase;(iv) a phosphotransacylase and a short chain fatty acid kinase; and (v) an alcohol acyltransferase.6. The microorganism according to claim 3 , wherein the microorganism expresses the following enzymes:(a) an acyl-CoA oxidase, such as ACX4; and(b) an acyl-CoA thioesterase, such as 4HBT.7. The microorganism according to claim 3 , wherein the microorganism expresses the following enzymes:{'i': 'Arabidopsis thaliana', '(a) ACX4, suitably from ; and'}{'i': 'Arthrobacter', '(b) 4HBT, suitably from sp.'}8. A microorganism adapted to conduct the following steps:(a) biologically converting isobutyryl-CoA into methacrylyl-CoA by expression of an acyl-CoA oxidase; and(b) biologically converting methacrylyl-CoA into a C1 to C20 methacrylic acid esterby expression of an ...

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27-06-2019 дата публикации

(meth)acrylic conductive material

Номер: US20190194368A1
Принадлежит: Osaka Organic Chemical Industry Co Ltd

(wherein R1 represents a hydrogen atom or a methyl group; and R2 represents an alkyl group having 1-10 carbon atoms, which may have a hydroxyl group or a halogen atom, or an alkoxyalkyl group having 2-12 carbon atoms, which may have a hydroxyl group); and the (meth)acrylic elastomer has a weight average molecular weight of 1,200,000 to 10,000,000 and a molecular weight distribution (weight average molecular weight/number average molecular weight) of 1-6.

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28-07-2016 дата публикации

METHOD AND APPARATUS FOR PRODUCING POLYMER AND METHOD AND APPARATUS FOR PRODUCING ORGANIC FILM

Номер: US20160215391A1
Принадлежит: FLOSFIA INC.

Provided is a method and an apparatus for producing a novel polymer that is easy and convenient to control the reactivity and excellent in film thickness control and a method and an apparatus for producing an organic film. A production apparatus includes: a first means for turning a raw-material solution containing an organic compound into a mist or droplets by an atomization or a droplet-formation; a second means for carrying the mist or droplets onto a substrate using a carrier gas; and a third means for subjecting the mist or droplets to a thermal reaction by heating on the substrate. Using the production apparatus, an organic film, such as a polymer film, is formed by atomizing or forming droplets from, for example, a raw-material solution containing the organic compound, such as a monomer, delivering a mist or droplets generated by the atomization or the droplet-formation to a substrate with a carrier gas, and, after the delivery, subjecting the mist or the droplets to a thermal reaction by heating on the substrate. 1. A method for producing a polymer by polymerization from a monomer , comprising:a first step of turning a raw material solution containing the monomer into a mist or droplets by an atomization or a droplet-formation;a second step of carrying the mist or droplets onto a substrate using a carrier gas; anda third step of subjecting the mist or droplets to a thermal reaction by heating on the substrate.2. The method of claim 1 , wherein the monomer is a vinyl monomer the raw-material solution contains a radical polymerization initiator.3. The method of claim 1 , wherein the raw-material solution contains water.4. The method of claim 1 , wherein the raw-material solution contains an organic solvent.5. The method of claim 1 , wherein the raw-material solution contains no solvent.6. The method of claim 1 , wherein the heating is carried out from 80° C. to 600° C.7. A polymer produced by the method of .8. An apparatus for producing a polymer claim 1 , ...

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06-08-2015 дата публикации

MICROBIOLOGICAL PRODUCTION OF 3-HYDROXYISOBUTYRIC ACID

Номер: US20150218601A1
Принадлежит: Evonik Roehm GmbH

The present invention relates to a cell which has been modified in comparison with its wild type in such a way that it is capable of forming more, by comparison with its wild, 3-hydroxyisobutyric acid or polyhydroxyalkanoates based on 3-hydroxyisobutyric acid via methylmalonate-semialdehyde or 3-hydroxybutyryl-coenzyme A as precursors. The invention also relates to a method of generating a genetically modified cell, to the genetically modified cell obtainable by these methods, to a method of producing 3-hydroxyisobutyric acid or polyhydroxyalkanoates based on 3-hydroxyisobutyric acid, to a method of producing methacrylic acid or methacrylic esters, and to a method of producing polymethacrylic acid or polymethacrylic esters. The present invention furthermore relates to an isolated DNA, to a vector, to the use of this vector for transforming a cell, to a transformed cell, and to a polypeptide. 1. A cell which has been genetically modified in comparison with its wild type in such a way that it is capable of forming more 3-hydroxyisobutyric acid from L-valine , as a carbon source , in comparison with its wild type , wherein more 3-hydroxyisobutyric acid is formed from 3-hydroxyisobutyryl-coenzyme A as a precursor , wherein activities of enzymes E , E , E , E , and Eare increased in the cell compared to its wild type , wherein:{'sub': '8', 'Eis a 3-hydroxyisobutyryl-coenzyme A hydrolase EC 3.1.2.4,'}{'sub': '60', 'Eis an enoyl-coenzyme A hydratase EC 4.2.1.17,'}{'sub': '61', 'Eis a 2-methylacyl-coenzyme A dehydrogenase EC 1.3.99.12'}{'sub': '79', 'Eis a 2-oxoisovalerate dehydrogenase EC 1.2.4.4, and'}{'sub': '80', 'Eis an amino acid transferase EC 2.6.1.42,'}{'i': 'Escherichia coli', 'wherein the cell is an cell.'}2Escherichia coli. A method of preparing a genetically modified cell which is capable of forming 3-hydroxyisobutyric acid or polyhydroxyalkanoates based on 3-hydroxyisobutyric acid using 3-hydroxybutyryl-coenzyme A claim 1 , as a precursors claim 1 , the method ...

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13-08-2015 дата публикации

COLORED PARTICLE FOR ELECTROWETTING DISPLAY, METHOD FOR PRODUCING COLORED PARTICLE FOR ELECTROWETTING DISPLAY, INK FOR ELECTROWETTING DISPLAY, AND ELECTROWETTING DISPLAY

Номер: US20150225500A1
Принадлежит: Sekisui Chemical Co., Ltd.

Provided is a colored particle used for an electrowetting display that is capable of enhancing the dispersibility in an ink for an electrowetting display. In the colored particle for an electrowetting display according to the present invention, a surface of the particle is formed from a compound containing only a carbon atom and a hydrogen atom as constituent atoms or a surface of the particle is formed from a compound in which the total amount of a carbon atom, a hydrogen atom, an oxygen atom, a nitrogen atom, and a sulfur atom is 95% by mass or more relative to 100% by mass of total of constituent atoms, and the mass ratio of the amount of the carbon atom to the total amount of the oxygen atom, the nitrogen atom, and the sulfur atom is 5 or more. 1. A colored particle for an electrowetting display havinga surface that is formed from a compound containing only a carbon atom and a hydrogen atom as constituent atoms; ora surface that is formed from a compound in which the total amount of a carbon atom, a hydrogen atom, an oxygen atom, a nitrogen atom, and a sulfur atom is 95% by mass or more relative to 100% by mass of total of constituent atoms, and the mass ratio of the amount of the carbon atom to the total amount of the oxygen atom, the nitrogen atom, and the sulfur atom is 5 or more.2. The colored particle for an electrowetting display according to claim 1 , wherein a surface-forming material to form the particle surface is a polymer of a polymerization component containing at least one selected from the group consisting of styrene claim 1 , isoprene claim 1 , isobutylene claim 1 , 1-butene claim 1 , 1-pentene claim 1 , 1-hexene claim 1 , 1-octene claim 1 , and butadiene or a hydrogenated product of the polymer; or a polymer of alkyl (meth)acrylate having an alkyl group having 12 to 18 carbon atoms.3. The colored particle for an electrowetting display according to claim 2 , wherein the surface-forming material to form the particle surface is a polymer of a ...

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02-07-2020 дата публикации

Photocurable resin composition

Номер: US20200207890A1
Принадлежит: Dexerials Corp

A photocurable resin composition which can improve adhesion between light transmitting members. The photocurable resin composition contains a monofunctional acrylic monomer having a heating residue of 85.0% or less after being heated at 60° C. for 30 minutes, a crosslinking agent, a photopolymerization initiator, and a softening agent composed of at least one of plasticizer and tackifier, and the heating residue after being heated at 60° C. for 30 minutes is less than 96.0%.

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20-08-2015 дата публикации

(METH)ACRYLATE COMPOSITION

Номер: US20150232591A1
Принадлежит:

Presented is a (meth)acrylate composition that can be cured even in an unirradiated portion that is not reached by light. The (meth)acrylate composition contains a compound having one or more vinyl groups in a molecular structure thereof. The compound has a ratio of a molecular weight thereof to a number of the vinyl groups of 300 or lower. The composition generates a heat of reaction during photopolymerization thereof, and the heat of reaction causes thermal polymerization of the composition. 15-. (canceled)6. A (meth)acrylate composition comprising a first compound having one or more vinyl groups in a molecular structure thereof , the first compound having a ratio of a molecular weight thereof to a number of the vinyl groups of 300 or lower , the composition not comprising a thermal polymerization initiator or a chain transfer agent , wherein the composition is curable by photopolymerization and thermal polymerization without agitation , the thermal polymerization caused by a heat of reaction generated during the photopolymerization7. The (meth)acrylate composition according to claim 6 , wherein the composition is curable in a portion that is not irradiated with light by the thermal polymerization induced by the photopolymerization.8. The (meth)acrylate composition according to claim 7 , wherein the composition further comprises one or more vinyl group-containing compounds other than the first compound claim 7 , including a second compound having one or more vinyl groups in a molecular structure thereof claim 7 , the second compound having a ratio of a molecular weight thereof to a number of the vinyl groups higher than 300 claim 7 , and a content of the first compound with respect to a total content of all vinyl group-containing compounds in the composition is 30 mass % or higher.9. The (meth)acrylate composition according to claim 8 , wherein the composition further comprises 0.1 to 20 mass % of a photopolymerization initiator with respect to a total mass of the ...

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10-08-2017 дата публикации

Apparatus for Addition of Droplets of a Monomer Solution to a Reactor

Номер: US20170225138A1
Принадлежит:

An apparatus for addition of droplets of a monomer solution for production of poly(meth)acrylate to a reactor for droplet polymerization, comprising at least one channel or a dropletizer head having, at its base, holes through which the solution is dropletized into the reactor, at least one of the following features being fulfilled: 224252635. The apparatus according to claim 1 , wherein the channels ( claim 1 , ) are sealed at their base by dropletizer plates () in which the holes () for dropletization of the solution are accommodated.325. The apparatus according to claim 1 , wherein the channels () are arranged in a star shape in the reactor.42425111. The apparatus according claim 1 , wherein the channels ( claim 1 , ) are arranged in a rotationally symmetric manner about the center of the reactor () claim 1 , the channels each projecting into the reactor () to different extents from the outer wall in the direction of the center of the reactor ().525. The apparatus according to claim 1 , wherein a plurality of parallel channels () in each case are aligned transverse to one another.6. The apparatus according to claim 1 , wherein at least one annular channel is included.7. The apparatus according to claim 1 , wherein the dropletizer head has a circular or homogeneous polygonal cross section.835. The apparatus according to claim 1 , wherein the holes () have a diameter in the range from 25 to 500 μm.935. The apparatus according to claim 1 , wherein the holes () have a distance from one another in the range from 1 to 100 mm.10. The apparatus according to claim 1 , wherein the number of holes relative to the area of the dropletizers is in the range from 1000 to 15 000 holes/m.11. (canceled) The invention proceeds from an apparatus for addition of droplets of a monomer solution for production of poly(meth)acrylate to a reactor for droplet polymerization, comprising at least one channel or a dropletizer head having, at its base, holes through which the solution is ...

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18-07-2019 дата публикации

METHOD OF MAKING FUNCTIONALIZED QUINACRIDONE PIGMENTS

Номер: US20190218397A1
Автор: FEICK Jason D., Wu Ziyan
Принадлежит:

Quinacridone pigments that are surface-functionalized with glycidyl methacrylate, maleic anhydride, or 4-methacryloxyethyl trimellitic anhydride to create a functionalized pigment. The functional groups are then activated to bond hydrophobic polymers, thereby coating the pigment with the hydrophobic polymers. The quinacridone pigments can be used for a variety of applications. They are well-suited for use in electro-optic materials, such as electrophoretic media for use in electrophoretic displays. 2. The method of claim 1 , wherein Ris —H or Ris —CH.3. The method of claim 1 , wherein the pigment comprising Formula VI and the acrylate monomers claim 1 , acrylate oligomers claim 1 , methacrylate monomers claim 1 , or methacrylate oligomers are ball milled together prior to reacting.4. The method of claim 1 , wherein the acrylate monomers or acrylate oligomers comprise lauryl acrylate claim 1 , 2-ethylhexyl acrylate claim 1 , hexyl acrylate claim 1 , n-octyl acrylate claim 1 , n-octadecyl acrylate claim 1 , or a combination thereof5. The method of claim 1 , wherein the methacrylate monomers or methacrylate oligomers comprise lauryl methacrylate claim 1 , 2-ethylhexyl methacrylate claim 1 , hexyl methacrylate claim 1 , n-octyl methacrylate claim 1 , n-octadecyl methacrylate claim 1 , or a combination thereof.6. The method of claim 1 , wherein the pigment is a magenta pigment. This application is a continuation of U.S. application Ser. No. 15/667,037, filed Aug. 2, 2017, now U.S. Pat. No. 10,196,523, which is a divisional application of U.S. application Ser. No. 15/347,995, filed Nov. 10, 2016, now U.S. Pat. No. 9,752,034, which claims priority to U.S. Provisional Patent Application No. 62/253,755, filed Nov. 11, 2015. All of the patents and applications disclosed herein are incorporated herein by reference in their entireties.This invention relates to colored electrophoretic displays, and more specifically to electrophoretic displays capable of rendering more than two ...

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27-08-2015 дата публикации

METHOD FOR PRODUCING RESIN COMPOSITE MATERIAL, AND RESIN COMPOSITE MATERIAL

Номер: US20150240004A1
Принадлежит:

There is provided a method for producing a resin composite material in which a synthetic resin is grafted on a carbon material and the deterioration of the resin is less likely to occur to develop high mechanical strength. A method for producing a resin composite material, comprising steps of providing a resin composition comprising a synthetic resin and a carbon material dispersed in the synthetic resin and having a graphene structure; and grafting the synthetic resin on the carbon material simultaneously with the step of providing the resin composition, or after the step of providing the resin composition, wherein the grafting step is performed by mixing an initiator in which a radical generated in thermal decomposition is a carbon radical with the synthetic resin and the carbon material and heating an obtained mixture. 1. A resin composite material comprising a synthetic resin and a carbon material having a graphene structure having a part of the synthetic resin grafted thereon and being dispersed in the synthetic resin ,a part of the synthetic resin being not grafted on the carbon material having a graphene structure and said part of the synthetic resin not grafted on the carbon material having an MFR of 15 g/10 min or less as measured according to JIS K7210.2. The resin composite material according to comprising 5 parts by weight or more of the carbon material having a graphene structure based on 100 parts by weight of the synthetic resin.3. The resin composite material according to further comprising a different type of resin from the synthetic resin.4. The resin composite material according to claim 1 , wherein the carbon material having a graphene structure is at least one selected from the group consisting of graphite claim 1 , exfoliated graphite claim 1 , and graphene.5. The resin composite material according to claim 1 , wherein the synthetic resin is a thermoplastic resin.6. The resin composite material according to claim 5 , wherein the thermoplastic ...

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27-08-2015 дата публикации

IMMERSION MEDIUM AND ITS LAYOUT IN AN OPTICAL SYSTEM

Номер: US20150241682A1
Принадлежит:

An immersion medium for microscopic or macroscopic examination of an object having an index of refraction between 1.0 to 1.70, a transmission between Lambda=0.30 to 1.2 μm, a transmission T=0.8 and higher, a temperature range from 0 degrees to 50 degrees Celsius, resistance to acids/bases and heat, a shear modulus of 129 to 500 Kpa, resistance to chemicals and environmental friendliness, as well as low inherent fluorescence. The immersion medium may be configured as an elastomer immersion. Embodiments of invention can include the layout of the immersion medium in the working position of an optical system. 1. An immersion medium for microscopic or macroscopic examination of an object , having an index of refraction between 1.0 to 1.70 , a transmission between Lambda=0.30 to 1.2 μm , a transmission T=0.8 and higher , a temperature range from 0 degrees to 50 degrees Celsius , resistance to acids/bases and heat , a shear modulus of 129 to 500 Kpa , resistance to chemicals and environmental friendliness , as well as low inherent fluorescence , wherein the immersion medium is configured as an elastomer immersion.2. The immersion medium of claim 1 , wherein in that the elastomer immersion is a non-toxic elastomer.3. The immersion medium of claim 1 , wherein the elastomer is a shape-stable claim 1 , elastically deformable plastic in the form of a siloxane or a natural polymer claim 1 , the glass transition point of which is situated below the temperature of use.4. The immersion medium of claim 3 , wherein the natural polymers are gelatin.5. The immersion medium of claim 3 , wherein the natural polymers are agarose.6. The immersion medium of claim 3 , wherein the polymers are vegetable polysaccharides (pectins).7. The immersion medium of claim 1 , wherein the elastomer immersion is a polydimethylsiloxane (PDMS) with or without an aqueous component.8. The immersion medium of claim 1 , wherein the elastomer immersion is a polymethylmethacrylate (PMMA).9. The immersion medium ...

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17-08-2017 дата публикации

Novel chain transfer agent and emulsion polymerization using the same

Номер: US20170233502A1
Принадлежит: Mitsubishi Chemical Corp

To provide a novel compound having both a surface-activating ability and a polymerization controlling ability. A compound represented by the following general formula (1) or (2): wherein, R 1 and R 3 are an organic group having the hydrophile-lipophile balance (HLB) determined by Griffin's method of 3 or more. The definitions of R 1 , R 2 , R 3 , R 4 , Z, p and q are described in the Description.

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25-08-2016 дата публикации

MONO DISPERSE POLYMER NANOPARTICLES, FUNCTIONALIZED NANOPARTICLES AND CONTROLLED FORMATION METHOD

Номер: US20160243051A1

A method produces polymer nanoparticles. Polymer solution is sprayed through a nozzle toward a collector. An electric field is created at the nozzle, such as by a voltage is applied to the nozzle to create the electric field. The voltage applied to the nozzle is from ˜10 (Kilovolt) to ˜30 (Kilovolt), distance from nozzle tip to collector is from ˜1 (centimeter) to ˜10 (centimeter) and the polymer concentration from ˜0.01% to ˜0.5% w/w. Preferably a grounded liquid collectors is used. The invention provides biocompatible monodisperse polymer nanoparticles having a size of less than ˜300 nm, preferably less than ˜150 nm. Payloads can be associated, and maintain efficacy, including more than one payload such as therapeutic agents and diagnostic agents on the same particles. Preferred particles are poly(methyl methacrylate) (PMMA-COOH) or acrylate analogues. 1. A method for forming polymer nanoparticles , the method comprising:spraying polymer solution through a nozzle toward a collector; andapplying an electric field around the nozzle while spraying, wherein a distance from nozzle tip to collector is from ˜1 (centimeter) to ˜10 (centimeter) and the polymer concentration from ˜0.01% to ˜0.5% w/w.2. The method of claim 1 , wherein the electric field is created by applying voltage to the nozzle; wherein the voltage is from ˜10 (Kilovolt) to ˜30 (Kilovolt).3. The method of claim 1 , wherein the collector comprises a liquid.4. The method of claim 3 , wherein the liquid comprises grounded de-ionized water.5. The method of claim 1 , wherein the polymer is a polymer comprising a polymer having a molecular weight of at least 5 kDa and sufficient viscoelasticity to transform into nanoparticles.6. The method of claim 1 , wherein the polymer comprises PMMA-COOH or acrylate analogues thereof.7. The method of claim 1 , wherein the acryl ate analogue is selected from poly(ethyl acrylate) claim 1 , Poly(butylacrylate) claim 1 , poly(methyl acrylate) claim 1 , copolymers of neutral ...

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03-09-2015 дата публикации

Process for the production of high internal phase emulsion foams

Номер: US20150246987A1
Принадлежит: Procter and Gamble Co

A method for polymerizing an open-cell foam including exposing an emulsion comprising a photoinitiator to an Ultraviolet light source, partially polymerizing the top surface of the emulsion, and moving the partially polymerized emulsion to a second polymerization stage.

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16-07-2020 дата публикации

DETERGENT FORMULATION CONTAINING MIXED-CHARGE POLYMERS

Номер: US20200224127A1
Принадлежит:

A detergent formulation comprises 0.5 to 10 weight-percent mixed-charge polymer and one to 10 weight-percent nonionic surfactant, where weight-percent is relative to total detergent formulation weight, and wherein the mixed-charge polymer comprises quaternary ammonium groups and carboxylate groups extending as pendant side groups from the polymer backbone. 2. The detergent formulation of claim 1 , wherein the weight-average molecular weight of the mixed-charge polymer is between 2 claim 1 ,000 and 100 claim 1 ,000 daltons as determined by gel permeation chromatography.3. The detergent formulation of claim 1 , wherein the detergent formulation contains less than one wt % chloride relative to detergent weight.4. The detergent formulation of claim 1 , wherein the detergent formulation further comprises 20-60 weight-percent inorganic builder relative to total detergent formulation weight.5. The detergent formulation of claim 1 , wherein the detergent formulation further comprises 1-30 weight-percent anionic surfactant based on total detergent formulation weight. The present invention relates to detergent formulations that contain mixed-charge polymers that can be substantially free of chloride or any halide.Mixed-charge polymers are useful in detergent formulations including automatic dishwashing detergent formulations and laundry detergent formulations. In automatic dishwashing, mixed-charge polymers reduce spotting on dishes. In laundry applications, mixed-charge polymers inhibit soil redeposition.Preparing mixed-charge polymers typically requires polymerization of a monomeric cationic chloride salt with an anionic monomer or monomers that are converted to anions after polymerization with the monomeric cationic chloride salt. The presence of chloride in such a process is problematic. Free chloride is corrosive to metal, including the metal typically used for polymerization reactors. Therefore, the reactors used for synthesis of mixed-charge polymers must be regularly ...

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17-08-2017 дата публикации

para-FURUTA POLYMER AND CAPACITOR

Номер: US20170236642A1
Принадлежит:

An organic polymeric compound called a para-Furuta polymer is characterized by polarizability and resistivity has repeating units of a general structural formula: 118-. (canceled)201. The compound of claim , wherein the resistive substitute Tails are independently selected from the list comprising polypropylene (PP) , polyethylene terephthalate polyester (PET) , polyphenylene sulfide (PPS) , polyethylene naphthalate (PEN) , polycarbonate (PP) , polystyrene (PS) , and polytetrafluoroethylene (PTFE).211. The compound of claim , wherein the resistive substitute Tails are independently selected from alkyl , aryl , substituted alkyl , substituted aryl , fluorinated alkyl , chlorinated alkyl , branched and complex alkyl , branched and complex fluorinated alkyl , branched and complex chlorinated alkyl groups , and any combination thereof , and wherein the alkyl group is selected from methyl , ethyl , propyl , butyl , I-butyl and t-butyl groups , and the aryl group is selected from phenyl , benzyl and naphthyl groups.221. The compound of claim , wherein it is preferable that the HOMO-LUMO gap is no less than 4 eV.231. The compound of claim , wherein it is even more preferable that the HOMO-LUMO gap is no less than 5 eV.241. The compound of claim , wherein at least one ionic liquid ion is selected from the list comprising [NR] , [PR] as cation and [—CO] , [—SO] , [—SR] , [—POR] , [—PR] as anion , wherein R is selected from the list comprising H , alkyl , and fluorine.27. The compound of claim 19 , wherein the linker group L is selected from the list comprising CH claim 19 , CF claim 19 , SiRO claim 19 , CHCHO claim 19 , wherein R is selected from the list comprising H claim 19 , alkyl claim 19 , and fluorine.28. The compound of claim 19 , wherein energy interaction of the ionic liquid ions is less than kT claim 19 , where k is Boltzmann constant and T is the temperature of environment.291928. An organic polymeric compound according to any of claims from to claim 19 , wherein ...

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24-08-2017 дата публикации

CLEANING COMPOSITION FOR SEMICONDUCTOR SUBSTRATE AND CLEANING METHOD

Номер: US20170240851A1
Принадлежит: JSR Corporation

A cleaning composition for a semiconductor substrate contains a solvent, and a polymer that includes a fluorine atom, a silicon atom or a combination thereof. The content of water in the solvent is preferably no greater than 20% by mass. The cleaning composition preferably further contains an organic acid which is a non-polymeric acid. The organic acid is preferably a polyhydric carboxylic acid. The acid dissociation constant of the polymer is preferably less than that of the organic acid. The solubility of the organic acid in water at 25° C. is preferably no less than 5% by mass. The organic acid is preferably a solid at 25° C. 1: A cleaning composition comprising:a solvent;a polyhydric carboxylic acid; anda polymer comprising a fluorine atom, a silicon atom or a combination thereof.2: The cleaning composition according to claim 1 , wherein a content of water in the solvent is no greater than 20% by mass.34-. (canceled)5: The cleaning composition according to claim 1 , wherein the polymer does not comprise an acid group claim 1 , or the polymer comprises an acid group and an acid dissociation constant of the polymer is smaller than an acid dissociation constant of the polyhydric carboxylic acid.6: The cleaning composition according to claim 1 , wherein a solubility of the polyhydric carboxylic acid in water at 25° C. is no less than 5% by mass.7: The cleaning composition according to claim 1 , wherein the polyhydric carboxylic acid is a solid at 25° C.814-. (canceled)15: The cleaning composition according to claim 1 , wherein a total content of the fluorine atom and the silicon atom in the polymer is 15% by mass or more claim 1 , and a content of the polymer with respect to a total solid content in the cleaning composition is 30% by mass or more.17: The cleaning composition according to claim 1 , wherein a content of the polyhydric carboxylic acid in the cleaning composition is 0.05% by mass or more.18: The cleaning composition according to claim 1 , wherein a ...

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30-08-2018 дата публикации

Nanostructures from Laser-Ablated Nanohole Templates

Номер: US20180243951A1
Принадлежит:

Solution casting a nanostructure. Preparing a template by ablating nanoholes in a substrate using single-femtosecond laser machining. Replicating the nanoholes by applying a solution of a polymer and a solvent into the template. After the solvent has substantially dissipated, removing the replica from the substrate. 1. A method for solution casting a nanostructure , the method comprising:preparing a template by ablating nanoholes in a substrate using single-femtosecond laser machining;replicating the nanoholes by applying a solution of a polymer and a solvent into the template; andafter the solvent has substantially dissipated, removing the replica from the substrate.2. The method of wherein the polymer solution comprises one of: cellulose acetate in acetone claim 1 , polycaprolactone (PCL) in chloroform claim 1 , PCL-polyethylene glycol in chloroform claim 1 , polydimethylsiloxane in heptane claim 1 , polymethylmethacrylate in toluene claim 1 , polyvinyl alcohol in de-ionized water claim 1 , and collodion in amyl acetate.3. The method of wherein the polymer is capable of forming a continuous film.4. The method of wherein the polymer is capable of forming a continuous film through the application of external energy.5. The method of wherein the polymer solution comprises a two percent (2%) solution by weight of one of: cellulose acetate in acetone claim 2 , polycaprolactone (PCL) in chloroform claim 2 , PCL-polyethylene glycol in chloroform claim 2 , and collodion in amyl acetate.6. The method of wherein the polymer solution comprises a solution between two percent (2%) and ten percent (10%) by weight of cellulose acetate in acetone.7. The method of wherein the polymer solution comprises a twenty five percent (25%) solution by weight of polydimethylsiloxane in heptane.8. The method of wherein the polymer solution comprises a solution between five percent (5%) and ten percent (10%) by weight of polymethylmethacrylate in toluene.9. The method of wherein the polymer ...

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31-08-2017 дата публикации

Apparatus for Production of Pulverulent Poly(Meth)Acrylate

Номер: US20170246607A1
Принадлежит: BASF SE

An apparatus for production of pulverulent poly(meth)acrylate, comprising a reactor or droplet polymerization, having an apparatus for dropletization of a monomer solution for the production of the poly(meth)acrylate, having holes through which the solution is dropletized, an addition point for a gas above the apparatus for dropletization, at least one gas withdrawal point on the periphery of the reactor and a fluidized bed. The outermost holes through which the solution is dropletized are positioned such that a droplet falling vertically downward falls into the fluidized bed and the hydraulic diameter at the level of the midpoint between the apparatus for dropletization and the gas withdrawal point is at least 10% greater than the hydraulic diameter of the fluidized bed. 1151351911111519111111911111. An apparatus for production of pulverulent poly(meth)acrylate , comprising a reactor () for droplet polymerization , having an apparatus for dropletization () of a monomer solution for the production of the poly(meth)acrylate , having holes through which the solution is dropletized , an addition point for a gas () above the apparatus for dropletization () , at least one gas withdrawal point () on the periphery of the reactor () and a fluidized bed () , wherein the outermost holes through which the solution is dropletized are positioned such that a droplet falling vertically downward falls into the fluidized bed () and the hydraulic diameter at the level of the midpoint between the apparatus for dropletization () and the gas withdrawal point () is at least 10% greater than the hydraulic diameter of the fluidized bed () , wherein the reactor () widens conically above the fluidized bed () to its maximum hydraulic diameter and the at least one gas withdrawal point () is positioned at the transition from the conical widening above the fluidized bed () to the cylindrical wall of the reactor () , wherein at the upper end of the widening the diameter of the conical widening ...

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17-09-2015 дата публикации

Control over Reverse Addition Fragmentation Transfer Polymerization Processes

Номер: US20150259449A1
Принадлежит:

A procedure for improved temperature control in controlled radical polymerization processes is disclosed. The procedure is directed at controlling the concentration of the persistent radical in ATRP and NMP polymerizations procedures and the concentration of radicals in a RAFT polymerization process by feeding a reducing agent or radical precursor continuously or intermittently to the reaction medium through one of more ports. 114-. (canceled)15. A RAFT polymerization process , comprising: i) at least a first free-radically polymerizable compound; and', 'ii) a RAFT agent;, 'a) forming a polymerization mixture, comprisingb) adding a free-radical initiator at a first temperature to the polymerization mixture; andc) minimizing uncontrolled exothermic reactions during the polymerization process by adding further amounts of the free-radical initiator at a controlled rate of addition to the polymerization mixture.16. The process of claim 15 , wherein the RAFT agent is one or more dithioesters.17. The process of claim 15 , wherein the controlled rate of addition controls the polymerization rate of the polymerization process.18. The process of claim 15 , wherein the controlled rate of addition controls the temperature of the polymerization process.19. The process of claim 15 , wherein the controlled rate of addition controls instantaneous concentrations of radicals in the polymerization process.20. The process of claim 15 , wherein the controlled rate of addition is adjusted to be commensurate with rate of radical-radical termination reactions in the process.21. The process of claim 15 , wherein the controlled rate of addition:a) controls propagation of polymeric chains formed in the polymerization mixture;b) maintains the polymerization mixture at or above the first temperature;c) allows conversion of the at least first free-radically polymerizable compound to exceed 80% conversion; ord) combinations thereof.22. The process of claim 15 , wherein the controlled rate of ...

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17-09-2015 дата публикации

CLEANING BLADE, AND IMAGE FORMING APPARATUS AND PROCESS CARTRIDGE USING THE CLEANING BLADE

Номер: US20150261171A1
Принадлежит: RICOH COMPANY, LTD.

A cleaning blade includes a supporting member, and a tabular elastic member. One end portion of the elastic member is fixed to the supporting member, and the other end portion is a free end portion whose tip edge is to be contacted with a member to be cleaned while rubbing the surface to remove a residual material therefrom. The tip portion of the free end portion of the elastic member ranging in length from 0 to 500 μm from the tip surface thereof includes at least a cured material of a curable compound and an elastic material of the elastic member. The elastic member satisfies the relationship, 0.05(%)≦[(t−t)/t]×100≦2%, wherein trepresents the maximum thickness of the tip portion of the elastic member, and trepresents the average thickness of the rear portion of the free end portion of the elastic member. 2. The cleaning blade according to claim 1 , wherein the cured material includes a cured material of at least one of an acrylate compound claim 1 , and a methacrylate compound.3. The cleaning blade according to claim 1 , wherein the cured material includes an ultraviolet cured material of an ultraviolet curable composition including the curable compound.4. The cleaning blade according to claim 1 , wherein the cured material includes a cured material of at least one of an alicyclic acrylate compound having 6 or more carbon atoms claim 1 , and an alicyclic methacrylate compound having 6 or more carbon atoms.5. The cleaning blade according to claim 4 , wherein the cured material includes a cured material of at least one of an alicyclic acrylate compound having 6 or more carbon atoms and including 2 to 6 functional groups claim 4 , and an alicyclic methacrylate compound having 6 or more carbon atoms and including 2 to 6 functional groups.6. The cleaning blade according to claim 4 , wherein the cured material includes a cured material of at least one of an alicyclic acrylate compound having 6 or more carbon atoms and a molecular weight of not greater than 500 claim 4 ...

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30-07-2020 дата публикации

METHOD OF MAKING FUNCTIONALIZED QUINACRIDONE PIGMENTS

Номер: US20200239695A1
Автор: FEICK Jason D., Wu Ziyan
Принадлежит:

Quinacridone pigments that are surface-functionalized with glycidyl methacrylate, maleic anhydride, or 4-methacryloxyethyl trimellitic anhydride to create a functionalized pigment. The functional groups are then activated to bond hydrophobic polymers, thereby coating the pigment with the hydrophobic polymers. The quinacridone pigments can be used for a variety of applications. They are well-suited for use in electro-optic materials, such as electrophoretic media for use in electrophoretic displays. 2. The pigment of claim 1 , wherein each Ris independently —H or —CH.3. An electrophoretic medium comprising a pigment of .4. An electro-optic display comprising a pigment of .5. A front plane laminate comprising a pigment of .7. The pigment of claim 6 , wherein each Ris independently —H or —CH.8. An electrophoretic medium comprising a pigment of .9. An electro-optic display comprising a pigment of .10. A front plane laminate comprising a pigment of . This application is a continuation of U.S. application Ser. No. 16/245,679, filed Jan. 11, 2019 (published as U.S. Patent Publication No. US 2019-0218397), which is a continuation of U.S. application Ser. No. 15/667,037, filed Aug. 2, 2017, now U.S. Pat. No. 10,196,523, which is a divisional application of U.S. application Ser. No. 15/347,995, filed Nov. 10, 2016, now U.S. Pat. No. 9,752,034, which claims priority to U.S. Provisional Patent Application No. 62/253,755, filed Nov. 11, 2015. All of the patents and applications disclosed herein are incorporated herein by reference in their entireties.This invention relates to colored electrophoretic displays, and more specifically to electrophoretic displays capable of rendering more than two colors using a single layer of electrophoretic material comprising a plurality of colored particles.The term color as used herein includes black and white. White particles are often of the light scattering type.The term gray state is used herein in its conventional meaning in the imaging ...

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07-10-2021 дата публикации

WATER-MEDIATED POLYESTER (METH)ACRYLATION SYSTEMS

Номер: US20210309766A1
Принадлежит:

A water-mediated process prepares a polymeric (meth)acrylation composition. In some embodiments, the process includes providing a stabilized aqueous solution including a (meth)acrylation component and a polyol monomer in a vessel under an inert atmosphere and adding a diacid monomer to the vessel under the inert atmosphere. In some embodiments, the process includes providing a stabilized aqueous solution including a (meth)acrylation component and a copolymer of a polyol monomer and a diacid monomer in a vessel under an inert atmosphere. The process further includes heating and removing water from the vessel under the inert atmosphere to produce the polymeric (meth)acrylation composition. The polymeric (meth)acrylation composition includes a (meth)acrylation polyester copolymer of the diacid monomer and the polyol monomer with the (meth)acrylation component conjugated to the (meth)acrylation polyester copolymer. In some embodiments, the polymeric (meth)acrylation composition is free of mineral acid and free of cytotoxic solvents, catalysts, and scavengers. 1. A water-mediated process of preparing a polymeric (meth)acrylation composition , comprising the steps of:providing a stabilized aqueous solution comprising at least one (meth)acrylation component and a polyol monomer in a vessel under an inert atmosphere;adding a diacid monomer to the vessel under the inert atmosphere; andheating and removing water from the vessel under the inert atmosphere to produce the polymeric (meth)acrylation composition;wherein the polymeric (meth)acrylation composition comprises a (meth)acrylation polyester copolymer of the diacid monomer and the polyol monomer with the at least one (meth)acrylation component conjugated to the (meth)acrylation polyester copolymer.2. The process of claim 1 , wherein the stabilized aqueous solution aids in preventing propagation and initiation of a free radical polymerization of the (meth)acrylate during the combining claim 1 , the adding claim 1 , and the ...

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15-09-2016 дата публикации

PHOTOCURABLE RESIN AND THREE-DIMENSIONAL PRINTING SYSTEM

Номер: US20160264696A1
Принадлежит:

A photocurable resin composition for three-dimensional printing which is visible-light curable is provided, comprising a photosensitive prepolymer in a range of 76.5 wt % to 96.8 wt %, a photoinitiator in a range of 0.01 wt % to 5 wt %, an auxiliary photoinitiator in a range of 0.01 wt % to 15 wt %, and a solvent in a range of 0.01 to 10 wt %. A three-dimensional printing system comprises: an accommodation unit, a lifting unit, a formation unit, and a control unit. The accommodation unit is for accommodating a printing material. The formation unit, which is connected to the lifting unit, can be driven by the lifting unit so as to move with respect to a light emission unit. The control unit, coupled to the lifting unit, controls motion of the lifting unit. The light emission unit may be a mobile electronic device, a display device, or a digital television. 1. A photocurable resin composition for three-dimensional printing , comprising:a photosensitive prepolymer in a range of 76.5 wt % to 96.8 wt %, a photoinitiator in a range of 0.01 wt % to 5 wt %, an auxiliary photoinitiator in a range of 0.01 wt % to 15 wt %, and a solvent in a range of 0.01 to 10 wt %, whereinthe photocurable resin composition is visible-light curable;the photosensitive prepolymer comprises at least one selected from the group consisting of butyl acrylate, methyl methacrylate, isobornylacrylate, hydroxyethyl methacrylate, caprolactone acrylate, isodecylacrylate, polyethylene glycol monoacrylate, 2-phenoxyethyl methacrylate, 1,6-ethylene glycol diacrylate, dipropylene glycol diacrylate, ethoxylated bisphenol A diacrylate, propoxylated neopentyl glycol diacrylate, triethylene glycol dimethacrylate, trimethylol propane triacrylate, pentaerythritol triacrylate;the photoinitiator comprises at least one selected from the group consisting of a benzoin indium-based compound, a benzoin acyl compound, a benzene-based compound, an acyl phosphorus oxide, a benzophenone-based compound, a thioxanthone based ...

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01-10-2015 дата публикации

FLAME-RESISTANT FIBER BUNDLE, CARBON FIBER BUNDLE, AND PROCESSES FOR PRODUCING THESE

Номер: US20150274860A1
Принадлежит:

A process for producing a flame-resistant fiber bundle, the process comprising a step in which a flame-resistant fiber bundle (1) having a single-fiber density ρof 1.26 g/cmto 1.36 g/cmis brought into contact sequentially with a heater group having a surface temperature Tof 240° C. to 400° C. under the following conditions (A), (B), and (C) to obtain a flame-resistant fiber bundle (2) having a single-fiber density ρof 1.33 g/cmto 1.43 g/cm: (A) the heater Hwith which the fiber bundle is brought into contact “n+1”-thly has a highter temperature than the heater Hwith which the fiber bundle is brought into contact “n”-thly; (B) the total contact time between the fiber bundle and the heater group is 10 seconds to 360 seconds; and (C) the contact time between the fiber bundle and each heater is 2 seconds to 20 seconds. 1. A flame-resistant fiber bundle configured by a single fiber group having a single-fiber fineness of 0.8 dtex to 5.0 dtex ,{'sup': 3', '3, 'wherein an average density of a single fiber is 1.33 g/cmto 1.43 g/cm, and a variation coefficient CV of the density in the fiber bundle is 0.2% or less.'}2. The flame-resistant fiber bundle according to claim 1 , the fiber bundle configured by a group of single fibers each having a kidney-type cross-sectional shape in which a length of major axis a is 10 μm to 32 μm claim 1 , a length of minor axis b is 6 μm to 20 μm claim 1 , a groove depth c is 0.1 μm to 3.0 μm claim 1 , and an aspect ratio a/b is 1.3 to 1.8.3. The flame-resistant fiber bundle according to claim 1 ,{'sup': '13', 'wherein a degree of orientation π (2θ=25° peak), which is obtainable by wide-angle X-ray analysis, is 68% to 74%, a ratio “A/S×100%” of an area A at the spectrum peak in the vicinity of 135 ppm, which is obtainable by solid state C-NMR, to the whole spectrum area S is 14% to 17%.'}4. A carbon fiber bundle configured by a group of carbon fibers each having a kidney-type cross-sectional shape in which a length of major axis a is 5 μm to 16 ...

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21-09-2017 дата публикации

STORAGE AND MIXING SYSTEM FOR PASTY CEMENT COMPONENTS AND METHOD THEREFOR

Номер: US20170265922A1
Принадлежит: HERAEUS MEDICAL GMBH

Storage and mixing systems for pasty two-component polymethyl methacrylate bone cements comprise a tubular cartridge having a cylindrical inner chamber, a cartridge head, which closes one end of the tubular cartridge at the front side, a partition that is disposed axially in the cylindrical inner chamber of the cartridge. The partition divides the cylindrical inner chamber of the cartridge bounded by the cartridge head into two cavities that are spatially separated from one another, wherein a first pasty cement component is present in the first cavity and a second pasty cement component is present in the separate second cavity. The systems further comprising two dispensing plungers axially displaceable in the two cavities of the cartridge, wherein the dispensing plungers close the two cavities on the back side of the cavities situated opposite the cartridge head, a bending device for deforming the partition, wherein the bending device is axially movable in the cartridge and is disposed, or is to be disposed, behind the dispensing plungers, as seen from the cartridge head, wherein the bending device has a deflection surface that is inclined with respect to the axis of the cartridge and pushes the partition laterally in the direction of the inside wall of the cartridge when the bending device is pushed into the cartridge.

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08-10-2015 дата публикации

INITIATION OF CONTROLLED RADICAL POLYMERIZATION FROM LACTIDE MONOMER

Номер: US20150284485A1

A lactide-functionalized polymer is synthesized by polymerizing a monomer capable of undergoing radical polymerization (e.g., styrenic, vinylic, acrylic, etc.) using a brominated lactide initiator via atom transfer radical polymerization (ATRP). In some embodiments of the present invention, the brominated lactide initiator is 3-bromo-3,6-dimethyl-1,4-dioxane-2,5-dione prepared by reacting lactide with N-bromosuccinimide in the presence of benzoyl peroxide. 5. The method as recited in claim 4 , wherein the monomer is selected from a group consisting of styrene claim 4 , butyl acrylate claim 4 , methyl acrylate claim 4 , 2-ethylhexyl acrylate claim 4 , ethyl acrylate claim 4 , 2-ethylhexl methacrylate claim 4 , ethyl methacrylate claim 4 , butyl methacrylate claim 4 , and combinations thereof.6. The method as recited in claim 4 , wherein the monomer is styrene.7. The method as recited in claim 4 , wherein the monomer is butyl acrylate.8. The method as recited in claim 4 , wherein the step of polymerizing a monomer using the brominated lactide initiator via atom transfer radical polymerization (ATRP) comprises the step of preparing a catalytic copper/ligand complex comprising a copper(I) complex and a ligand with a slight excess of copper prior to adding the brominated lactide initiator to the copper/ligand complex.9. The method as recited in claim 4 , further comprising the step of:reacting lactide with N-bromosuccinimide in the presence of benzoyl peroxide to prepare the bromated lactide initiator.10. The method as recited in claim 4 , further comprising the step of:{'sub': '2', 'reacting lactide with bromine (Br) in the presence of benzoyl peroxide to prepare the bromated lactide initiator.'}12. The method as recited in claim 11 , wherein the monomer is selected from a group consisting of styrene claim 11 , butyl acrylate claim 11 , methyl acrylate claim 11 , 2-ethylhexyl acrylate claim 11 , ethyl acrylate claim 11 , 2-ethylhexl methacrylate claim 11 , ethyl ...

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04-10-2018 дата публикации

PROCESS FOR PREPARING VINYL ACETATE-ETHYLENE COPOLYMERS BY EMULSION POLYMERIZATION

Номер: US20180282440A1
Принадлежит: Wacker Chemie AG

Subjects of the invention are processes for preparing vinyl acetate-ethylene copolymers in the form of their aqueous dispersions or water-redispersible powders by means of radically initiated emulsion polymerization and optional subsequent drying of the resultant polymer dispersions, characterized in that the emulsion polymerization of vinyl acetate, ethylene and optionally one or more further ethylenically unsaturated monomers is carried out in the presence of one or more protective colloids in one or more Taylor reactors. 1. A process for preparing vinyl acetate-ethylene copolymers in the form of their aqueous dispersions or water-redispersible powders by means of radically initiated emulsion polymerization and optional subsequent drying of the resultant polymer dispersions , the process comprising emulsion polymerization of vinyl acetate , ethylene and optionally one or more further ethylenically unsaturated monomers in the presence of one or more protective colloids in one or more Taylor reactors , the Taylor reactor comprising an external reactor wall , a rotor located within the external reactor wall , a reactor base , and a reactor lid , the wall , rotor , base , and lid defining a toroidal reactor volume.2. The process according to claim 1 , wherein the external reactor wall has an inner wall and the rotor has an outer wall claim 1 , the inner wall of the external reactor wall and the outer wall of the rotor each having a cylindrical geometry.3. The process according to claim 1 , wherein the Taylor reactor is equipped with at least two metering devices.46. The process according to claim 2 , wherein at least one metering device is mounted on the reactor base and/or at least one metering device () is mounted on a bearing of the rotor and/or at least one metering device is mounted in the external reactor wall.56. The process according to claim 4 , wherein a plurality of metering devices () are mounted locally in succession in the external reactor wall in a flow ...

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12-09-2019 дата публикации

Acrylic polymer composition

Номер: US20190276634A1
Принадлежит: Zeon Corp

Provided is an acrylic polymer composition comprising an acrylic polymer and a polyfunctional organic compound having a urea group, wherein the acrylic polymer composition has less than 50% decrease in molecular weight of the acrylic polymer when heated under conditions of 190° C. and 144 hours in air.

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