КОМПОЗИЦИИ ПОКРЫТИЙ ДЛЯ МАРКИРОВКИ ПОДЛОЖЕК

Настоящее изобретение относится к композиции покрытия для маркировки подложек, ее получению и использованию, которая включает цветообразователь, полимерное связующее, растворитель, дополнительные компоненты и соль металлоорганического соединения с амином формулы !! где X - Si или В, R3, R4 и R5 - Н, алкил, аллил, или R3 и R4 вместе с атомом азота образуют морфолиновое кольцо; о и р=0 или 1, Е и F выбраны из ! ! R6 и R7 = Н, R1 - фенил или R1 вместе с R2 образуют остаток, выбранный из ! ! Технический результат - получение новых композиций для получения подложек и маркированных подложек на их основе. 7 н. и 6 з.п. ф-лы.

СТАБИЛИЗИРОВАННЫЕ ОРГАНОБОРАНОВЫЕ ИНИЦИАТОРЫ ПОЛИМЕРИЗАЦИИ И СПОСОБНЫЕ К ПОЛИМЕРИЗАЦИИ КОМПОЗИЦИИ

Настоящее изобретение относится к стабилизированным и способным к полимеризации композициям. Описана способная к полимеризации стабилизированная адгезивная композиция из двух частей, содержащая в одной части борорганическое соединение, способное к образованию соединений, образующих свободные радикалы, которое содержит комплекс органоборана и амина или органоборатную соль, одно или более соединение, способное к свободнорадикальной полимеризации, и одно или более соединение, содержащее дигидрокарбилгидроксиламин, и во второй части содержит одно или более соединение, способное к свободнорадикальной полимеризации, и декомплексообразующий агент, способный превращать борорганическое соединение в соединение, образующее свободные радикалы, при контактировании двух частей. Также описан способ полимеризации, включающий контактирование компонентов указанной выше способной к полимеризации композиции, а также описан способ связывания двух или более соединений вместе, который содержит совместное контактирование ...

ТВЕРДОЕ ГОРЮЧЕЕ

Изобретение относится к прикладной химии, а именно к твердым горючим (ТГ) для прямоточных воздушно-реактивных двигателей (ПВРД) активно-реактивных снарядов (АРС). Твердое горючее содержит органическое горючее-связующее, ультрадисперсный порошок высокоэнергетического металла и карборан и/или фенилкарборан. В качестве горючего-связующего ТГ содержит смесь эпоксидной смолы, дибутилфталата, отвердителя и диаминдиолеата при определенном соотношении компонентов. Состав ТГ обеспечивает сохранение целостности изготовленных из него газогенерирующих элементов в условиях больших перегрузок АРС при выстреле из орудия и его работе путем улучшения механических характеристик ТГ при одновременно высоких энергетических и других характеристиках. 3 з.п. ф-лы, 1 табл.

ИНИЦИИРУЕМЫЕ ОРГАНОБОРАН-АМИННЫМ КОМПЛЕКСОМ ПОЛИМЕРИЗУЮЩИЕСЯ КОМПОЗИЦИИ, СОДЕРЖАЩИЕ СИЛОКСАНОВЫЕ ПОЛИМЕРИЗУЮЩИЕСЯ КОМПОНЕНТЫ

... 1. Полимеризующаяся композиция, содержащая а) органоборан-аминный комплекс, b) один или более мономеров, олигомеров или полимеров, имеющих олефиновую ненасыщенность, которые способны полимеризоваться свободнорадикальной полимеризацией, с) одно или более соединений, олигомеров или форполимеров, имеющих силоксановую главную цепь и реакционные остатки, способные к полимеризации, и d) катализатор полимеризации одного или более соединений, олигомеров или форполимеров, имеющих силоксановую главную цепь и реакционные остатки, способные к полимеризации. 2. Полимеризующаяся композиция по п.1, дополнительно содержащая катализатор полимеризации одного или более соединений, олигомеров или форполимеров, имеющих силоксановую главную цепь и реакционные остатки, способные к полимеризации, в которой соединение, которое вызывает диссоциацию комплекса, хранят отдельно от комплекса и катализатор полимеризации одного или более соединений, олигомеров или форполимеров, имеющих силоксановую главную цепь, хранят ...

СТАБИЛИЗИРОВАННЫЕ ОРГАНОБОРАНОВЫЕ ИНИЦИАТОРЫ ПОЛИМЕРИЗАЦИИ И СПОСОБНЫЕ К ПОЛИМЕРИЗАЦИИ КОМПОЗИЦИИ

... 1. Способная к полимеризации композиция из двух частей, содержащая в одной части борорганическое соединение, способное к образованию соединений, образующих свободные радикалы, и одно или более соединение, содержащее дигидрокарбилгидроксиламин или алициклический гидроксиламин или оксид нитрила дигидрокарбиламина или алициклического гидроксиламина, и во второй части содержит одно или более соединение, способное к свободно-радикальной полимеризации. 2. Композиция из двух частей по п.1, в которой вторая часть дополнительно содержит декомплексообразующий агент, способный превращать борорганическое соединение в соединение, образующее свободные радикалы, при контактировании двух частей. 3. Композиция из двух частей по п.2, в которой борорганическое соединение представляет собой комплекс органоборана и амина или органоборатную соль. 4. Композиция из двух частей по п.3, в которой борорганическое соединение представляет собой комплекс органоборана и амина. 5. Композиция из двух частей по п.3, в которой ...

ТЕРМОАССОЦИАТИВНЫЕ И ОБМЕННЫЕ СОПОЛИМЕРЫ, СОДЕРЖАЩАЯ ИХ КОМПОЗИЦИЯ

Полимерные композиции на основе сшитого силоксанила

Внутренняя антиадгезионная смазка для формования изделий из полиуретана, полиольная композиция для формования изделий из полиуретана и способ формования изделий из полиуретана

Сущность изобретения: изделие формуют из композиции, в состав коИэобретение относится к переработке полиуретана в изделие и может быть использовано в различных областях промышленности. Полиуретановые отформованные (литьевые ) изделия находят все возрастающее применение в автомобильной промышленности, при производстве фурнитуры и изготовлении предметов доторой наряду с полиолом, катализатором и полиизоцианатом входит внутренняя антиадгезионная смазка, содер- держащая соль металла, выбранную из группы; включающей: стеарат .цинка, лаурат цинка, дилаурат цинка, стеарат кальция, стеарат кадмия и стеарат лития и модифицирующую добавку - соединение, выбранное из группы, включающей: инициированный аминоэтил амином полипропиленоксид мол.м, 27о, (продукт реакции этилендиамина с пропиленоксидом из расчета ., 15,5 моль окиси пропилена на 1 моль водорода с эквивалентным веtcoM 89, продукт реакции 1 моль ами- ноэтилпиперазина с 6 моль пропилен- оксида или триизопропаноламином, при следующем соотношении ...

ALKYL BORON COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE

Self amalgamating silicone rubber tape containing silica reinforcing filler, carbon black, metal powder and platinum catalyst

A self-amalgamating conductive silicone rubber composition comprises the following components (A) 100 parts by weight organopolysiloxane with a high degree of polymerisation ; (B) up to 100 parts by weight silica powder reinforcing filler with a relative surface area of at least 50 m<2>/g ; (C) up to 100 parts by weight quasi-reinforcing filler for increasing the weight of the composition, having a relative surface area of at least 2 m<2>/g ; (D) up to 150 parts by weight carbon black (D1) and/or 1-400 parts by weight metal powder (D2) ; (E) 0.1-10 parts by weight platinum catalyst (E1) and a cross-linking agent (E2a) or organic peroxide (E2b) ; and (F) 0.1-20 parts by weight boron-containing additive, chosen so that the boron/silicon atom ratio in the composition is 1:100-500.

VERWENDUNG VON UNTER EINFLUSS VON UV-LICHT UND BORATONIUM-PHOTOINITIATOREN KATIONISCH HÄRTENDEN SILIKONZUSAMMENSETZUNGEN ZUR HERSTELLUNG VON FLACHDICHTUNGEN,INSBESONDERE VON ZYLINDERKOPFDICHTUNGEN

Verfahren zur Herstellung von besonders vorteilhaften flammwidrigen, halogenfreien Polyurethan-Polyharnstoffen

Lagerstabile Epoxidharz-Zusammensetzung

Die vorliegende Erfindung betrifft die Verwendung von Boronsäuren zur Erhöhung der Lagerstabilität von Epoxidharz-Zusammensetzungen sowie Epoxidharz-Zusammensetzungen umfassend ein Epoxidharz, einen Härter, einen Härtungsbeschleuniger sowie eine Boronsäure.

Preparation of dialkoxyvinylboranes

A dialkoxyvinylborane of the general formula H2C=CHB(OR)2, wherein R is an alkyl group, preferably containing 1 to 4 carbon atoms, is made by heating a solution of a metal trialkoxyvinylborate of the formula H2C=CHB(OR)3MgX, wherein X is a chlorine or bromine atom, in an anhydrous inert solvent having a boiling point higher than the decomposition temperature of the metal trialkoxyvinylborate until the latter is thermally decomposed and collecting the dialkoxyvinylborane which distils from the solution. The solvent may be substituted or unsubstituted hydrocarbon or an ether. Distillation of the dialkoxyvinylborane may be started as soon as the decomposition of the metal compound is reached, and by introducing fresh metal trialkoxyvinyl borate continuously to replace that which is decomposed, the process can be performed continously. Reaction temperatures of 150 DEG C. to 275 DEG C. are preferred and the process may be effected at atmospheric or reduced pressures. Examples describe the preparation ...

Metal carboxylates containing boron

Metal organic compounds containing both cobalt and nickel bound to boron are effective adhesion promoters for bonding rubber to brass-coated metal used as a reinforcement.

Improvements in or relating to the processing of natural rubber

The use of a cobalt boroacylate containing from 11 to 23% by weight cobalt as a peptiser activator is also disclosed.

Curable acrylate or methacrylate compositions

A curable composition based on a curable (meth) acrylate component, such as methyl (meth) acrylate, 2-ethylhexyl (meth) acrylate; an organoborane initiator component, such as triethylborane; a vinyl ether component, such as bis [4-(vinyloxy) butyl] isophthalate, 1,4-Butanediol divinyl ether, diethyleneglycol divinyl ether or triethyleneglycol divinyl ether; and an activator for the organoborane component, such as Lewis acids, carboxylic acids, phosphoric acids, anhydrides, isocyanates and combinations thereof. The composition exhibits good storage stability and good bonding properties when used to bond low surface energy substrates, such as polyolefins.

Stabilized silicon grease composition

A treated silica, for use in a silicone grease composition (see Division C3), is prepared by merely mixing a finely divided silica (fume, xerogel or aerogel) with boric acid, trimethoxyboroxine (methylmetaborate) or a trialkylborate in which the alkyl radicals contain from 1 to 5 C atoms. Preferably the mixture is heated at 100 DEG to 250 DEG C. for 1 to 6 hours. The boron compound is preferably used in amount to provide from 0.001 to 1 pt. (by wt.) of B per 5 to 17 pts. of silicon. In Example (3) (H) 10 pts. of silica aerogel were mixed with 0.75 pt. of trimethoxyboroxine (0.135 pt. B) and the resulting mixture was heated at 200 DEG C. for 5 hours.ALSO:A stabilized grease composition comprises (1) a major amount of a silicone oil, (2) a minor amount of a finely divided silica as thickener, and (3) a stabilizing amount of boric acid, trimethoxyboroxine (methylmetaborate) or a trialkyl borate in which the alkyl radicals contain from 1 to 5 C atoms. The greases are made either by blending ...

POLYIMIDE-FORMING COMPOSITIONS

... 1,255,028. Laminates. MONSANTO CO. 24 Dec., 1968 [2 Jan., 1968], No. 61302/68. Heading B5N. [Also in Divisions B2 and C3] A polyimide-forming composition comprises a mixture of (A) an aromatic tri- or tetracarboxylic acid or an ester or ammonium salt thereof; (B) an aromatic at least a diprimary amine; and (C) at least 0-1% by wt. of (A)+(B) of a thermal stabilizer which is an alkyl acid ester or an ammonium or substituted ammonium salt of phosphoric acid or of an oxyacid of boron or sulphur. Extensive lists of possible ingredients (A), (B) and (C) are given; the proportions of (A) : (B) may vary from 70% molar excess of (B) to 10% excess of (A). The compositions may also comprise solvents, catalysts, fillers, extenders, adhesion promoters and blowing or foaming agents. They may be used in the manufacture of fibre-reinforced composites e.g. using glass or asbestos fibre or cloth. Glass cloth used in Examples is surface-treated with 3-aminopropyl triethoxysilane. 12-ply laminates are made ...

Improvements in or relating to polymeric materials comprising polyolefins

Polyolefins are stabilized by blending them with a minor proportion of an organo-boron compound consisting of an ester of an oxy-acid of boron, or a boronic acid or ester thereof, or a borinic acid or ester. The organo-boron compounds contain a radical of at least 6 carbon atoms. The polyolefin is preferably made by a low-pressure process using a Ziegler-type catalyst. The blends may also include known stabilizers and anti-oxidants. The polyolefines may be polyethylene or polypropylene. The Specification contains an extensive list of suitable organo-boron compounds of which tristearyl borate, 2, 6- di-tertiary butyl-phenyl din-butylborate, and 2, 6-di-tertiary butyl, 4-methylphenyl din-butyl borate are used in the examples. Other stabilizers mentioned are sodium carbonate, cadmium and calcium stearates, polymeric glycidyl polyethers and tin alkyl esters. Specification 867,027 is referred to.

Improvements in and relating to resins

A stabilized composition comprises an acrylonitrile-containing resin and from 0,02 to 5% by weight, based on the weight of resin of pyridine borane or an alkyl pyridine borane in which the alkyl radical, or radicals, contains 1 to 10 carbon atoms. The acrylonitrile resins used are polyacrylonitrile and copolymers of at least 25% by weight of acrylonitrile with comonomers such as vinyl and vinylidene chlorides, vinyl and allyl acetates, methyl methacrylate, styrene and butadiene. The pyridine boranes may be used in conjunction with other stabilizers, e.g. dioctyl tin maleate, tetrabutyl tin, trimethyl tin chloride, tributyltin acetate, tributyl phosphine, tripropenyl and triisooctyl phosphites, tributyl phosphonite, 5-ethyl-2-(2-ethylhexyloxy)-2-oxo-4-propyl-1, 3, 2-dioxaphosphorinane and the diglycidyl ether of bisphenol-A. The stabilizers are preferably added to solutions of the resins in solvents such as acetonitrile, acetone, cyclohexanone, dimethyl-formamide and acetamide, ethylene ...

STABILIZER FOR HALOGEN-CONTAINING POLYMERS

... 1524270 Borate-ester salts; polymer stabilizers HOECHST AG 19 Nov 1976 [21 Nov 1975] 48357/76 Heading C3K [Also in Division C2] Halogen-containing polymers are stabilized using a mixture of a primary stabilizer and a co-stabilizer comprising a metal salt of an acidic basic acid ester of a polyhydric alcohol of formula HO-CH2[CH(OH)]n-CH2OH, where n = 2-5; the molar ratio of basic acid to the polyhydric alcohol is from 1 : 0À5 to 1 : 4, and the salt contains cations of an alkali metal, an alkaline earth metal, Zn, Cu, Cd, Sn, Pb, Mn, Co, Ni, Al, Zr, La or Ce. In the examples, the polyhydric alcohols used are sorbitol, mannitol, xylitol and pentaerythritol (comparative) and the metals of the borateester-salt are Ca, Mg, Al, Na, Sr, Sn-II, Pb-II, Cd, Ni-II, Cu, and Zn.

PROCEDURE FOR THE PRODUCTION OF NEW SPIRO CYCLI BORON CONNECTIONS

USE OF SALTS OF SUPERCACIDS AS STABILIZER IN VINYLHALOGENIDPOLYMEREN

VERWENDUNG VON SPIROCYCLISCHEN BORSAEUREESTERN ALS FLAMMHEMMER IN KUNSTSTOFFEN, FLAMMHEMMEND AUSGERUESTETE KUNSTSTOFFE SOWIE SPIROCYCLISCHE BORSAEUREESTER

The use of spirocyclic boric acid esters of the formula as flame inhibitors for plastics. R1 and R2 are either, independently of one another, divalent radicals of alcohols having from 2 to 6 OH groups or together are the tetravalent radical of pentaerythritol, Z is an N-base, and m is an integer from 1 to 3.

COATING COMPOSITIONS FOR SUBSTRATE MARKING

ACCELERATED AN ORGANOBORAN INITIATING AND POLYMERIZE-CASH COMPOSITIONS

FLAME-ADVERSE RESIN COMPOSITIONS AND PROCEDURES

PROCEDURE FOR THE PRODUCTION OF NEW BORON SILICON CONNECTIONS

FLAME-FASTEN FROM PLASTICS WITH BORON EN CONNECTIONS

PROCEDURE FOR THE PRODUCTION OF NEW BORON SILICON CONNECTIONS

PROCEDURE FOR THE IMPROVEMENT OF THE COLD FLOW STABILITY OF POLYMERS

PROCEDURE FOR THE HAERTEN OF REACTION ADHESIVES.

PROCEDURE FOR THE PRODUCTION OF NEW SPIRO CYCLI BORON CONNECTIONS

BORON CONNECTIONS ABSTENTION STORABLE ONE, AEROB HAERTENDE PLASTIC MASSES, IN PARTICULAR REACTION ADHESIVES.

SURFACE-TREATED METALLKOMPONENT FOR THE REINFORCEMENT OF STRUCTURES FOR PRODUCTS OF VULCANIZED ELASTOMEREM MATERIAL AND FROM IT MANUFACTURED ARTICLE

TRANSPARENT FIREPROOF LAMINATES AND THEIR PRODUCTION

USE OF UNDER INFLUENCE OF UV LIGHT AND BORATONIUM PHOTOINITIATOREN KATIONISCH HARDENING SILICONE COMPOSITIONS FOR THE PRODUCTION OF GASKETS, IN PARTICULAR OF CYLINDER HEAD GASKETS

USE OF ACCELERATORS FOR THE POLYMERIZATION AND/OR NETWORKING OF POLYORGANOSILOXANEN WITH INTERLACE-CASH FUNCTIONAL GROUPS, APPROPRIATE COMPOSITIONS

Procedure for the improvement of the glowing firmness of mats bound with phenol formaldehyde resins and molded articles from glass and/or mineral wool

Method of crosslinking glycosaminoglycans

A new hydrogel made of crosslinked glycosaminoglycans, particularly crosslinked hyaluronic acid, chondroitin or chondroitin sulfate, having reversible linkages using boronic acid or boroxole derivatives leading to new benefits. Glycosaminoglycans that are crosslinked via an alkoxyboronate ester anion formed between a diol portion of a diol-functional moiety grafted to a first glycosaminoglycan and a boronate hemiester grafted to a second glycosaminoglycan.

Incorporation of boron complex into resin

Complexes, compositions, articles of manufacture, and method for making the same are provided herein. In one embodiment, a borate-polyol complex may be prepared by reacting a boron-containing compound and a polyol to form a reaction mixture and then neutralizing the reaction mixture to form a neutralized borate-polyol complex. The neutralized borate- polyol complex may then be used in combination with polymeric resins to form adhesive products, among other material products, which products can be in manufacturing articles.

Using occluding fluids to augment additive manufacturing processes

The present disclosure relates to the use of occluding fluids, such as a high-density fluid (a "z-fluid") or a low-density fluid (an "a-fluid"), to displace resin within a vat during 3D printing. Further, an a-fluid may act as a protective boundary for a 3D printing resin wherein the a-fluid sits on top of the printing resin. Another embodiment of the disclosure provides a process of assessing which regions of a computer-aided design (CAD) model take advantage of a buoying force supplied by the occluding fluid, such that fewer support structures are needed for printing a final CAD model compared to printing the CAD model without the occluding fluid.

POLYURETHANES CONTAINING ORGANOBORON SALTS

Method of curing a coating composition comprising a radical curable compound and an organoborane-amine complex

A method of curing a coating composition and a method of forming a cured coating on an automobile component are provided. The coating composition comprises a radical polymerizable compound and an organoborane-amine complex having an organoborane initiator, an amine blocking agent, and water. The method of curing the coating composition comprises the steps of combining the organoborane-amine complex, the radical polymerizable compound, and water to form the coating composition. Carbon dioxide is introduced into the coating composition or into a composition including at least one of the organoborane-amine complex, the radical polymerizable compound, and water prior to forming the coating composition. Carbonic acid is formed in situ within the coating composition through reaction of the water and carbon dioxide. The organoborane-amine complex is decomplexed with the carbonic acid thereby separating the organoborane initiator and the amine blocking agent. The radical polymerizable compound ...

Siloxane compound and process for producing the same

A siloxane compound comprises a plurality of siloxane repeating units and at least a portion of the siloxane repeating units are cyclosiloxane repeating units conforming to a specified structure. A process for producing such siloxane compounds is also provided. A process and kit for producing a cross-linked silicone polymer using the described siloxane compounds is also provided. A light emitting diode (LED) comprises an encapsulant, and the encapsulant comprises a cross-linked silicone polymer produced from the described siloxane compounds.

Solvent-free organosiloxane composition and its use

ORGANOPOLY SILOXANE ELASTOMER

Surface-treated metal component for reinforcing structures for manufactured pr oducts made of elastomeric material and an article of manufacture comprising t he same

ANTISTATIC POLYURETHANE-UREA DISPERSIONS

HYDRAULIC FLUIDS

CUMYLPHENOL AND THEIR USE IN POLYMERS

INTERNAL MOLD RELEASE COMPOSITIONS

COUPLING AGENTS

FLUID LOSS CONTROL ADDITIVE AND CEMENT COMPOSITIONS COMPRISING SAME

A fluid loss control additive comprising a crosslinked polymer and sugar and cement compositions comprising the same. In one embodiment, the fluid loss control additive comprises a polymer and a sugar connected by a pH-sensitive crosslink. In some embodiments, the polymer is a polyvinyl alcohol, and the sugar is a sugar alcohol such as sorbitol.

COPOLYMER, TREATMENT AGENT FOR PAPER, AND TREATED PAPER

Disclosed is a treatment agent for paper comprising a fluorine-containing copolymer having a repeat unit (a) derived from a fluorine-containing monomer represented by general formula (I): CH2=C(-X)-C(=O)-Y-[-(CH2)m-Z-]p-(CH2)n-Rf; a repeat unit (b) derived from at least one amino monomer represented by general formula (II-1): (see formula II-1) or a derivative thereof; and a repeat unit (c) derived from a pyrrolidone monomer represented by general formula (III): ( see formula III) The treatment agent for paper provides paper having high oil resistance and high water resistance.

ANTISTATIC POLYURETHANE-UREA DISPERSIONS

Disclosed is a dispersion of a polyurethaneurea polymer in a continuous phase. This dispersion contains 0.1 to 5 parts by weight of an ionizable, nonvolatile salt per 100 parts by weight of polyurethaneurea polymer. The dispersion of this invention is useful in preparing static dissipative coatings, films, membranes and the like.

COMPOSITIONS ELASTOMERIQUES ORGANOPOLYSILOXANIQUES VULCANISABLES A CHAUD A CARACTERISTIQUES PHYSIQUES AMELIOREES

La présente invention concerne des compositions élastomériques organopolysiloxaniques vulcanisables à chaud, formées par mélange d'une gomme diorganopolysiloxanique A), d'une charge renforçante B), d'un peroxyde D: et d'un groupe d'au moins 3 additifs choisis parmi un organohydrogénopolysiloxane E), un polymère organofluoré F), un composé organosiloxanique comportant, relié à l'atome de silicium, au moins un groupe acroyloxyalcoyle ou méthacroyloxyalcoyle G, un composé renfermant du bore H). Ces compositions sont notamment utilisables pour réaliser des élastomères de silicone vulcanisables à chaud.

BORON-SILICON COMPOUNDS SUITABLE FOR USE AS HYDRAULIC FLUIDS

Novel compounds of the general formula: (I) wherein:(a) each R1 is a hydrocarbyl group, or a group of the formula: -(OR5)n-OR6, (i) -R5-(OR5)n-OR6, (ii) or (iii) and each R1 may be the same as, or different from, any other group R1.(b) R2 is a group as defined for R1, or a group of the formula: -O(R5O)nSi(R1)3 (iv) and each group R2 may be the same as, or different from, any other group R2. (c) each of R3 and R4 is independently a group of the formula: R2-Si-(R1)2 (v) OR3 (vi) -B-OR4 (vi) -(R5O)n-R6 (vii) (d) R5 is an alkylene or an arylene group and each R5 may be the same as, or different from, any other group R5,(e) R6 is a hydrocarbyl group of hydrogen and each group R6 may be the same as, or different from, any other group R6,(f) n is zero or an integer and each n may be the same as, or different from, any other n. The compounds are useful as water scavengers, particularly for hydraulic fluids, as well as in paints, lubricating oils and electrical oils.

SILICONE AQUEOUS EMULSION FORMING AN ELASTOMER BY CROSSLINKING FOLLOWING WATER WITHDRAWAL

La présente invention concerne une émulsion thixotrope de silicone, réticulant en un élastomère par élimination de l'eau dans les conditions ambiantes, caractérisée en ce qu'elle comporte, en poids : (A) - 100 parties d'une émulsion du type huile dans eau d'un .alpha.,.omega.-(dihydroxy)polydiorganosiloxane stabilisée anioniquement et/ou non-ioniquement, (B) - 1 à 15 parties d'une charge siliceuse en poudre de renforcement, (C) - 0 à 250 parties d'une charge minérale autre que la charge siliceuse B, (D) - 0,01 à 2 parties d'un sel d'organoétain, (E) - 0,1 à 5 parties d'un dérivé oxygéné du bore, ladite émulsion ayant un pH compris entre 4 et 8 et une teneur en extraits secs d'au moins 50 %. Procédé de préparation des émulsions. Utilisation des émulsions selon l'invention à la réalisation de joints élastomères silicone en particulier dans l'industrie du bâtiment.

SPIROCYCLIC BORON COMPOUNDS, A PROCESS FOR THEIR MANUFACTURE AND THEIR USE AS A FLAME-RETARDANT ADDITIVE

USING OCCLUDING FLUIDS TO AUGMENT ADDITIVE MANUFACTURING PROCESSES

The present disclosure relates to the use of occluding fluids, such as a high-density fluid (a "z-fluid") or a low-density fluid (an "a-fluid"), to displace resin within a vat during 3D printing. Further, an a-fluid may act as a protective boundary for a 3D printing resin wherein the a-fluid sits on top of the printing resin. Another embodiment of the disclosure provides a process of assessing which regions of a computer-aided design (CAD) model take advantage of a buoying force supplied by the occluding fluid, such that fewer support structures are needed for printing a final CAD model compared to printing the CAD model without the occluding fluid.

ANTISTATIC AND LIGHT-STABLE THERMOPLASTIC POLYCARBONATE MOULDING COMPOUNDS

The invention relates to compositions comprising A) 50 to 90 wt% of at least one polymer selected from the group consisting of aromatic polycarbonate, aromatic polyestercarbonate and aromatic polyester, B) 5 to 40 wt% of polymer comprising B.1 at least one rubber-modified vinyl (co)polymer comprising B.1.1 80 to 95 wt%, based on B.1, of at least one vinyl monomer and B.1.2 5 to 20 wt%, based on B.1, of one or more rubber-elastic polybutadiene-containing graft bases, where B.1 comprises polybutadiene-containing rubber particles which are grafted with the vinyl monomers B.1.1 and which comprise inclusions of vinyl (co)polymer consisting of the vinyl monomers B.1.1, und a vinyl (co)polymer matrix which is not bound to these rubber particles and not included within rubber particles, consisting of the vinyl monomers B.1.1, and optionally B.2 further rubber particles grafted with vinyl monomers and composed of B.2.1 5 to 75 wt%, based on B.2, of at least one vinyl monomer on B.2.2 25 to95 wt% ...

INITIATOR FOR POLYMERISING AND/OR CROSS-LINKING POLYORGANOSILOXANES WITH CROSS-LINKABLE FUNCTIONAL GROUPS, CORRESPONDING COMPOSITIONS AND THEIR USES

La présente invention a pour objet un amorceur de polymérisation et/ou de réticulation activable thermiquement, de monomères, oligomères et/ou de polymères de nature polyorganosiloxane à groupements organofonctionnels comprenant un dérivé du bore de formule (I): (A)xB(R')y dans laquelle les symboles R' sont identiques ou différents et représentent un radical alkyle ou alcényle en C1-C12, un radical alkoxy en C1-C12, un radical phényle substitué par au moins un élément électroattracteur, un radical aryle contenant au moins deux noyaux aromatiques tel que biphényle, naphtyle, éventuellement substitué par au moins un élément électroattracteur, notamment atome d'halogène (fluor tout particulièrement), ou un groupement électroattracteur notamment un groupement CF3, NO2, CN, un radical -C2H4-Si(Q)3 avec les symboles Q identiques ou différents représentant un groupe alkyle ou alkoxy en C1 à C10 ou un oligomère siloxane inférieur à 10 atomes de silicium. Elle vise également une composition réticulable ...

RADIATION-CURING RESIN COMPOSITION AND PREPREG

A radiation-curing resin composition that includes a resin component that includes an epoxy resin and/or oxetane resin having a naphthalene structure or a biphenyl structure, a boron-based diaryliodonium salt polymerization initiator represented by a specific formula at 0.005 to 0.5 mol per kg of the resin component, and a viscosity adjusting agent, the resin composition having a viscosity at 50°C of at least 50 Pa.cndot.s, and a prepreg obtained by impregnating a fiber reinforcement with such a resin composition. This resin composition has excellent reactivity, and a prepreg formed from this resin composition and a fiber reinforcement is used for producing a composite material/member suitable for the aerospace field in particular.

SILOXANE COMPOUND AND PROCESS FOR PRODUCING THE SAME

A siloxane compound comprises a plurality of siloxane repeating units and at least a portion of the siloxane repeating units are cyclosiloxane repeating units conforming to a specified structure. A process for producing such siloxane compounds is also provided. A process and kit for producing a cross-linked silicone polymer using the described siloxane compounds is also provided. A light emitting diode (LED) comprises an encapsulant, and the encapsulant comprises a cross-linked silicone polymer produced from the described siloxane compounds.

CROSSLINKED SILOXANYL POLYMER COMPOSITIONS

A polymeric composition comprisingat least onecovalently cross-linked siloxanyl polymercluster which is further cross-linked by a boron compound, wherein the concentration of boron is in the range 0.005-0.160wt.%.

METAL ORGANIC COMPOUNDS AND THEIR USE

Metal organic compounds containing both cobalt and nickel bound to boron are effective adhesion promoters for bonding rubber to brass-coated metal used as a reinforcement.

MIXED ESTERS OF BORIC ACID AND PHOSPHORIC ACID WITH POLYOLS, THEIR PREPARATION AND THEIR USE

Described are mixed boric acid/phosphoric acid esters which may be obtained by subjecting at least one phosphorus compound capable of ester formation and at least one boron compound capable of ester formation simultaneously to an esterification reaction with at least one polyol and/or a derivative thereof capable of ester formation. Such esters may be prepared in an aqueous medium and find use in the flame-proofing treatment of a variety of materials, as acid catalysts for acid-curing synthetic materials, for controlling boron deficiencies in cultivated plants, and in many other fields of application.

Verfahren zur Herstellung von Tri-mercapto-borsäure-estern

Verfahren zur Herstellung von selbstklebenden Organopolysiloxanelastomeren

Verfahren zur Herstellung von Dialkoxyvinylboran

Procédé de préparation de composés organo-métalliques

Stabilisiertes Olefinpolymer

Körper aus oxydhaltigen anorganischen Blähmaterialien und Kunstharzbindemitteln mit verbesserter Formbeständigkeit bei Einwirkung von Feuer und/oder hohen Temperaturen sowie Verfahren zu dessen Herstellung

Aminoplast or phenoplast resin binders for materials

Binders for making materials based on wood consist of a mixture of synthetic wood glues e.g. phenoplasts or aminoplasts, a wood preservative and organic solvents, with the addition of a cyclic compound (I) containing 5 to 8 atoms of which 2 or 3 are O atoms. Improved resistance to attack by animals or micro-organisms, without lowering other properties.

Verfahren zum Stabilisieren hochmolekularer linearer thermoplastischer Polycarbonate

Verfahren zur Herstellung von siloxanbeschichtetem Trennpapier

Verwendung von Borsäureestern als neutronenabsorbierendes Material

Verfahren zum Stabilisieren hochmolekularer Stoffe, die vollständig oder zum überwiegenden Teil aus verzweigten oder unverzweigten Kohlenwasserstoffen aufgebaut sind

Verfahren zur Verbesserung der Wetterfestigkeit fester organischer nichttextiler Substrate

Verfahren zur Verbesserung der Stabilität von Polyolefinen

Mit Phenolformaldehydharzen gebundene Glas- und/oder Mineralwolle und Verfahren zu ihrer Herstellung

Selbstklebendes Kautschukband und Verwendung des Bandes zum Herstellen einer elektrischen Isolation auf einem elektrischen Leiter

Verfahren zum Stabilisieren fester Polymermassen oder nichttextiler Gebilde aus Polymeren

Thermoplastische Polyester enthaltende Formmasse

FLAMING CELEBRATION PRODUCT.

FLAMING CELEBRATION PRODUCT.

BORIC ACID ESTER OF 2,2,2?TRIS?(BROMOMETHYL)?ETHANOL

Compositions of siloxanes and borates

MATERIAU FORMANT ECRAN CONTRE LES NEUTRONS ET PROCEDE POUR SA PREPARATION

L'INVENTION CONCERNE UN MATERIAU CONSTITUANT UN BOUCLIER CONTRE LES NEUTRONS, ET SON PROCEDE DE PREPARATION. LE MATERIAU EST UN PRODUIT DE POLYMERISATION D'UN MELANGE MONOMERE COMPOSE D'UN MONOMERE DE BASE CONTENANT A TITRE DE CONSTITUANT ESSENTIEL AU MOINS UN MONOMERE CHOISI PARMI DES METHACRYLATES D'ALCOYLE CONTENANT 1 A 4ATOMES DE CARBONE DANS LE RADICAL ALCOYLE ET DU STYRENE ET UN ESTER D'ACIDE BORIQUE QUI CONTIENT A TITRE DE CONSTITUANT ESSENTIEL AU MOINS UN POLYOL CONTENANT AU MOINS DEUX RADICAUX HYDROXYLE ALCOOLIQUES DANS SA MOLECULE ET 3 A 16ATOMES DE CARBONE, LE RAPPORT MOLAIRE A ENTRE LE POLYOL ET LES ATOMES DE BORE DANS L'ESTER D'ACIDE BORIQUE FORME A PARTIR DU POLYOL ETANT DANS LA GAMME 0,6A4, LA TENEUR B ( EN POIDS) DU BORE DANS LE TOTAL DU MELANGE MONOMERE ETANT DANS LA GAMME 1B6. LES PLAQUES COULEES EN MATERIAU SELON L'INVENTION SONT PARTICULIEREMENT EFFICACES CONTRE LES NEUTRONS THERMIQUES.

SCORCH RETARDERS FOR HALOGENATED BUTYL RUBBER

COMPOSITION FOR TRANSPARENT ELEMENTS, CONTAINING EPOXY RESIN HARDENED WITH ADDITIVES OF TRIMETHOXYBOROXINE AND BENZYLIC ALCOHOL

AN AQUEOUS SILICONE EMULSION IS CROSS-LINKABLE ELASTOMER IN BY WATER REMOVAL

A method for improving the properties of weather resistance of organic substrates solid in particular of polyolefin resins

Stabilizing for substances of raised molecular weight, made entirely or mainly of hydrocarbons ramified or not

A method for stabilizing phenylene polyoxydes

COATED FILLERS FOR POLYMERS

Method for increasing the recyclability of a polyamide used in sintering

The present invention relates to a method for increasing the recyclability of a polyamide in a sintering process, wherein at least 4000 ppm of at least one acid is incorporated in the polyamide, said acid being selected from: the acids of general formula HxPyOz in which x, y and z are integers selected in the range from 1 to 7, boric acid, the salts of these acids, their esters, their anhydrides and mixtures thereof.

COMPOSITIONS CONTAINING BORANE OR CARBORANE CAGE COMPOUNDS AND RELATED APPLICATIONS

Compositions comprising a polymer-containing matrix and a filler comprising a cage compound selected from borane cage compounds, carborane cage compounds, metal complexes thereof, residues thereof, mixtures thereof, and/or agglomerations thereof, where the cage compound is not covalently bound to the matrix polymer. Methods of making and applications for using such compositions are also disclosed. 1. A composition comprising:a matrix comprising a polymer, wherein said polymer comprises less than 90 weight percent of a poly(conjugated diene), wherein said polymer comprises less than 90 weight percent of a polysiloxane; anda filler comprising a mixture of cage compounds selected from the group consisting of a borane cage compound, a carborane cage compound, a metal complex thereof, a residue thereof, and agglomerations thereof, wherein said cage compounds comprise at least 7 cage atoms,wherein said cage compounds are not covalently bound to said polymer.2. The composition of claim 1 , wherein said polymer comprises less than 10 weight percent of a poly(conjugated diene) claim 1 , wherein said polymer comprises less than 10 weight percent of a polysiloxane.3. The composition of claim 1 , wherein one of said cage compounds comprises a borane cage compound and/or a carborane cage compound having 12 cage atoms claim 1 , wherein said cage compound has an icosahedral structure.4. The composition of claim 1 , wherein one of said cage compounds comprises one or more pendant groups selected from the group consisting of a Cto Cn-alkyl claim 1 , a hydroxy claim 1 , a carboxy claim 1 , an epoxy claim 1 , an isocyanate claim 1 , a primary amine claim 1 , a silyl claim 1 , and an alkoxy silyl.5. The composition of claim 1 , wherein one of said cage compounds is selected from the group consisting of:{'sub': 2', 'n', 'n+2, '(a) a closo-carborane having the general formula CBH, wherein n is in the range of from 5 to 10;'}{'sub': x', '2', 'n', 'n+2−x', '1', '20, '(b) a closo-carborane ...

THICKENING OF FLUIDS

An aqueous fluid contains an aqueous solution or dispersion of a polymer to thicken the fluid together with a cross linking agent to enhance the viscosity of the fluid by crosslinking the polymer, wherein the crosslinking agent comprises supporting structures bearing functional groups to react with the polymer molecules and has a mean particle size of 2 nanometer or more. The supporting structures may be nanoparticles and the functional groups may be boronic acid groups. The concentration of boron in a thickened fluid may be low and in some instances there is resistance to applied pressure. The fluid may be a hydraulic fracturing fluid. 126-. (canceled)27. An aqueous fluid comprising an aqueous solution or dispersion of a polymer to thicken the fluid and a cross linking agent to enhance the viscosity of the fluid by crosslinking the polymerwherein the crosslinking agent comprises supporting structures bearing functional groups to react with the polymer molecules, wherein the functional groups are covalently attached to the supporting structures, and wherein the crosslinking agent has a mean particle size in a range from 1 nm to 1000 nm.28. A fluid according to claim 27 , wherein the crosslinking agent has a mean particle size in a range from 2 nm to 200 nm.29. A fluid according to claim 27 , wherein the crosslinking agent has a mean particle size in a range from 5 nm to 100 nm.30. A fluid according to claim 27 , wherein the polymer concentration is in a range from 0.5 to 20 g/liter.31. A fluid according to claim 27 , wherein the polymer concentration is no more than 2 g/liter.32. A fluid according to claim 27 , wherein the supporting structures have the functional groups attached thereto through linking groups.33. A fluid according to claim 27 , wherein the number of functional groups on a supporting structure is at least 1000.34. A fluid according to claim 27 , wherein the quantity of cross linking agent is no more than 20% by weight of the polymer.35. A fluid ...

Polymer Composition for Microelectronic Assembly

Embodiments in accordance with the present invention encompass polymer compositions that act as both a tack agent and a fluxing agent for the assembly of microelectronic components onto a variety of substrate materials. Such polymer compositions embodiments encompass a sacrificial polymer, a carrier solvent, a thermal acid generator and, optionally, formic acid. 1. A polymer composition comprising:a sacrificial polymer comprising a polycarbonate having a molecular weight (Mw) from 5,000 to 200,000;a carrier solvent;formic acid; anda thermal acid generator/fluxing agent (TAG/FLAG) selected from:di(4-tert-butylphenyl)iodonium trifluorophenylborate,dimethylanilinium tetrakis(pentafluorophenyl)borate,pyridinium trifluoromethanesulfonate,4-isopropyl-4′-methyldiphenyliodonium tetrakis(pentafluorophenyl)borate,di(4-tert-butylphenyl)iodonium trifluoromethanesulfonate,(2-(4-methoxynaphthalen-1-yl)-2-oxoethyl)dimethylsulfonium tetrakis(pentafluorophenyl)borate,p-methoxybenzyldimethylanilinium trifluoromethanesulfonate,or mixtures thereof.2. The polymer composition of where the TAG/FLAG is di(4-tert-butylphenyl)iodonium trifluorophenylborate.3. The polymer composition of where the TAG/FLAG is dimethylanilinium tetrakis(pentafluorophenyl)borate.4. The polymer composition of where the TAG/FLAG is pyridinium trifluoromethanesulfonate.5. The polymer composition of where the TAG/FLAG is 4-isopropyl-4′-methyldiphenyliodonium tetrakis(pentafluorophenyl)borate.6. The polymer composition of where the TAG/FLAG is di(4-tert-butylphenyl)iodonium trifluoromethanesulfonate claim 1 , or mixtures thereof.7. The polymer composition of where the TAG/FLAG is (2-(4-methoxynaphthalen-1-yl)-2-oxoethyl)dimethylsulfonium tetrakis(pentafluorophenyl)borate.8. The polymer composition of where the TAG/FLAG is p-methoxybenzyldimethylanilinium trifluoromethanesulfonate claim 1 , or mixtures thereof.9. The polymer composition of where the sacrificial polymer is selected from poly(propylene carbonate) or a ...

Curable Composition

The invention relates to a composition comprising (A) at least 5% by weight of en organic prepolymer P having at least two water-crossilnkable organosilicon end groups, (B) 0.01% to 3.0% by weight of boric acid and/or bone ester, and (C) 0.01% to 3.0% by weight of an amine component. Additionally disclosed is a method for the curing of these compositions and also the use of boric acid and/or boric esters and an amine component a condensation catalyst.

MOISTURE CURABLE RESIN COMPOSITION AND CURED PRODUCT

An object of the present invention is to provide a moisture curable resin composition that is appropriately excellent in workability and is capable of making initial moisture curing properties and moisture curing properties after a storage stability test compatible. 1. A moisture curable resin composition , containing (A) to (C) components described below , wherein the moisture curable resin composition contains 0.03 parts by mass to 0.9 parts by mass of the (C) component with respect to 100 parts by mass of the (A) component.(A) Component: a curable resin that has a main chain skeleton containing polyoxyalkylene and has a hydrolyzable silyl group(B) Component: a moisture curing catalyst containing a fluorine-based compound(C) Component: zeolite having a pore diameter of 5 angstroms to 30 angstroms2. The moisture curable resin composition according to claim 1 , wherein a hydrolyzable silyl group of the (A) component is an alkoxysilyl group.3. The moisture curable resin composition according to claim 1 , wherein a curable resin of the (A) component has urethane bonding on a main chain.4. The moisture curable resin composition according to claim 1 , wherein a viscosity of a curable resin of the (A) component at 25° C. is in a range of 5 Pa·s to 1000 Pa·s.5. The moisture curable resin composition according to claim 1 , wherein the moisture curable resin composition does not substantially contain an organic tin compound.6. The moisture curable resin composition according to claim 1 , wherein the (B) component is a complex containing boron trifluoride.7. The moisture curable resin composition according to claim 1 , wherein the (B) component is a boron trifluoride amine complex.8. The moisture curable resin composition according to claim 1 , wherein a content of the (B) component is 0.01 parts by mass to 0.9 parts by mass with respect to 100 parts by mass of the (A) component.9. The moisture curable resin composition according to claim 1 , further containing a silane ...

Color conversion composition, color conversion sheet, and light source unit, display and lighting device each comprising same

A color conversion composition that converts incident light into light having a longer wavelength than the incident light is described, the color conversion composition including the following components (A) and (B): component (A): an organic light-emitting material; and component (B): a resin whose molecular structure has a fluorene skeleton.

SINGLE STEP CREOSOTE/BORATE WOOD TREATMENT

Disclosed herein are preservative compositions and methods of using the same for reducing insect and microbial decay in wood. Also disclosed are wooden articles that have been treated with the compositions described herein. 13-. (canceled)4. A wood treatment composition formed by blending components comprising:(1) at least about 3% w/w of a reaction product of alkanolamine and borate; and(2) at least about 90% w/w creosote;wherein the borate comprises disodium octaborate tetrahydrate (DOT).5. The wood treatment composition of claim 4 , wherein the alkanolamine comprises a monoalkanolamine.6. The wood treatment composition of claim 4 , wherein the alkanolamine comprises a C-Cmonoalkanolamine.7. The wood treatment composition of claim 4 , wherein the alkanolamine comprises monoethanolamine.8. The wood treatment composition of claim 4 , wherein the blending is carried out at an elevated temperature such that substantially all water has been removed from the composition.9. The wood treatment composition of claim 8 , wherein the composition comprises at least about 95% w/w creosote and is greater than 98% w/w free of water.10. The wood treatment composition of claim 4 , wherein the creosote comprises heavy bunker C fuel oil.11. The wood treatment composition of claim 10 , wherein the creosote comprises about 40 to 60% w/w heavy bunker C fuel oil.12. The wood treatment composition of claim 4 , wherein at least about 40% w/w of the borate is disodium octaborate tetrahydrate (DOT).13. The wood treatment composition of claim 4 , wherein the borate comprises disodium octaborate tetrahydrate (DOT) and boric acid.14. The wood treatment composition of claim 4 , wherein the reaction product is prepared by reacting the borate with the alkanolamine in water.15. The wood treatment composition of claim 4 , wherein the reaction product comprises unreacted borate.16. The wood treatment composition of claim 4 , wherein the composition further comprises biodiesel.17. The wood treatment ...

Ionic Polymer Compositions

A dielectric polymeric composition comprising a polymeric matrix comprising structural units derived from a polymerizable vinyl monomer; an ionic liquid comprising an organic cation and a balancing anion, wherein the ionic liquid is miscible or partially miscible with the polymerizable vinyl monomer, and wherein the concentration of ionic liquid in dielectric polymeric composition ranges from 0.5 to 30 wt. %; and less than 10 ppm of unreacted polymerizable vinyl monomer, based on the total weight of the composition, wherein an amount of unreacted polymerizable vinyl monomer in the composition is measured via HPLC. The polymeric matrix further comprises structural units derived from a polymerizable co-monomer comprising a functional group that has the ability to form hydrogen bonds within the polymeric matrix. The polymeric matrix further comprises a crosslinking agent, and wherein the polymeric matrix comprises covalent crosslinks between the crosslinking agent and the structural units derived from the polymerizable vinyl monomer. 1. A dielectric polymeric composition comprising:(a) a polymeric matrix, wherein the polymeric matrix comprises structural units derived from at least one polymerizable vinyl monomer;(b) an ionic liquid, wherein the ionic liquid comprises an organic cation and a balancing anion, wherein the ionic liquid is miscible or partially miscible with the at least one polymerizable vinyl monomer, and wherein the concentration of the ionic liquid in the dielectric polymeric composition ranges from about 0.5 wt. % to about 30 wt. %; and(c) less than about 10 ppm of unreacted polymerizable vinyl monomer, based on the total weight of the dielectric polymeric composition, wherein an amount of unreacted polymerizable vinyl monomer in the dielectric polymeric composition is measured via high performance liquid chromatography (HPLC).2. The dielectric polymeric composition of claim 1 , wherein the dielectric polymeric composition comprises a continuous ...

RESIN - FLUORINE-CONTAINING BORIC ACID COMPOSITE PARTICLES COMPOSITE MATERIAL

A composite material of resin—fluorine-containing boric acid composite particles comprising a resin, and a condensate of boric acid and a fluorine-containing alcohol represented by the general formula R-A-OH (wherein Ris a perfluoroalkyl group having 6 or less carbon atoms, or a polyfluoroalkyl group, in which some of the fluorine atom or atoms of the perfluoroalkyl group are replaced by a hydrogen atom or hydrogen atoms, and which contains a terminal perfluoroalkyl group having 6 or less carbon atoms and a perfluoroalkylene group having 6 or less carbon atoms; and A is an alkylene group having 1 to 6 carbon atoms, or comprising a resin, and a condensate of boric acid, the said fluorine-containing alcohol and an alkoxysilane at a molar ratio of 1.0 or less based on the fluorine-containing alcohol. These composite materials of resin—fluorine-containing boric acid composite particles has good adhesion to inorganic substrates, and the like. 1. A composite material of resin—fluorine-containing boric acid composite particles comprising: {'br': None, 'sub': 'F', 'R-A-OH \u2003\u2003[I]'}, 'a resin, and a condensate of boric acid and a fluorine-containing alcohol represented by the general formula{'sub': 'F', 'wherein Ris a perfluoroalkyl group having 6 or less carbon atoms, or a polyfluoroalkyl group, in which some of the fluorine atom or atoms of the perfluoroalkyl group are replaced by a hydrogen atom or hydrogen atoms, and which contains a terminal perfluoroalkyl group having 6 or less carbon atoms and a perfluoroalkylene group having 6 or less carbon atoms; and A is an alkylene group having 1 to 6 carbon atoms, or'} 'a resin, and a condensate of boric acid, the said fluorine-containing alcohol and an alkoxysilane at a molar ratio of 1.0 or less based on the fluorine-containing alcohol.', 'comprising2. The composite material of resin—fluorine-containing boric acid composite particles according to claim 1 , wherein the fluorine-containing alcohol represented by the ...

Adhesive composition containing ionic antistatic agent

An adhesive composition includes an acryl copolymer, a cross-linking agent, and an ionic antistatic agent represented by Formula 1, thereby exhibiting excellent antistatic property, as well as, significantly improved durability, maintaining excellent adhesiveness under severe conditions such as high temperature and high humidity atmospheres, and securing sufficient antistatic property even if used in a small amount.

Use of 4-bora-3a,4a-diaza-s-indacenes for security purposes

The invention relates to the use of one or more compounds of the 4-bora-3a,4a-diaza-s-indacene family for the preparation of a security element for a product, in particular a document, said security element comprising a polymer and said compound(s) being incorporated in said polymer, and to a method for ensuring the security of a product, in particular that of a document.

Composite material for the detection of chemical species

A composite material for sensing a chemical species in a medium is provided. The composite material includes a polymer having a glass transition temperature, a porosity promoter dispersed in the polymer in an amount such that the chemical species is transportable from the medium into the composite material at a temperature below the glass transition temperature, and a chemical indicator dispersed in the composite material, the chemical indicator providing an optical response varying with a concentration of the chemical species in the composite material.

Method for preparing a functionalized polyorganosiloxane

A method for preparing functionalized polyorganosiloxanes is disclosed. The method includes 1) combining starting materials including A) a boron—containing Lewis acid catalyst, and B) an organosilicon compound having an average, per molecule of at least 1 silicon bonded groups of the formula —OR2; wherein each R2 is an independently selected monovalent hydrocarbon group of 1 to 6 carbon atoms, thereby forming a catalyzed mixture; and thereafter 2) adding the catalyzed mixture into a starting material including C) an organohydrogensiloxane having at least 1 silicon bonded hydrogen atom per molecule, thereby preparing a product comprising the functionalized polyorganosiloxane and a by-product comprising HR2.

EPOXY RESIN COMPOSITION

An object of the present invention is to provide an epoxy resin composition capable of forming a cured epoxy resin product that exhibits excellent initial transparency and weatherability and excellent adhesion to various substrates. The present invention relates to an epoxy resin composition containing (A) an epoxy resin, (B) a polycarboxylic anhydride containing a structural unit represented by formula (1), and (C) a specific phosphonium compound 2. The epoxy resin composition according to claim 1 , wherein the epoxy resin (A) is at least one member selected from the group consisting of bisphenol-type epoxy resins claim 1 , phenol novolac-type epoxy resins claim 1 , glycidyl ester-type epoxy resins claim 1 , glycidyl ether-type epoxy resins claim 1 , amine-type epoxy resins claim 1 , alicyclic epoxy resins claim 1 , alicyclic glycidyl ether-type epoxy resins claim 1 , triazine-type epoxy resins claim 1 , and glycoluril-type epoxy resins.3. The epoxy resin composition according to claim 1 , wherein the epoxy resin (A) is at least one member selected from the group consisting of alicyclic glycidyl ether-type epoxy resins claim 1 , triazine-type epoxy resins claim 1 , and glycoluril-type epoxy resins.9. An adhesive material or coating material comprising the epoxy resin composition of .10. An automotive glazing material comprising the epoxy resin composition .11. An epoxy resin molded article formed by curing the epoxy resin composition according to .12. A method for forming a thin film comprising{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'applying the epoxy resin composition of onto a substrate, and'}curing the coated film to form a thin film with a thickness of 1 mm or less.13. A thin film with a thickness of 1 mm or less formed by curing the epoxy resin composition of .14. The thin film according to claim 13 , which is a coating material for displays. The present invention relates to an epoxy resin composition.Cured epoxy resin products obtained by curing an ...

RESIN COMPOSITION AND MOLDED ARTICLE

An object of the present invention is to provide a resin composition which can be detected both by X-ray radiation and by fluorescence or phosphorescence, and a molded article obtained from the resin composition. The present invention provides a resin composition containing a light-emitting substance and a radiopaque substance; in which the light-emitting substance is a near-infrared fluorescent material or a phosphorescent material. a radiopaque substance of the resin composition is any one of barium sulfate, bismuth oxide, bismuth subcarbonate, calcium carbonate, aluminum hydroxide, tungsten, zinc oxide, zirconium oxide, zirconium, titanium, platinum, bismuth subnitrate, and bismuth. A molded article can be obtained by processing any one of the resin compositions described above. 119-. (canceled)21. The method of producing a resin composition according to claim 20 ,wherein the near infrared fluorescent material is compatible with the resin.22. The method of producing a resin composition according to claim 20 ,wherein the content of the near-infrared fluorescent material in the resin composition is 0.001% by mass to 0.05% by mass.29. The method of producing a resin composition according to claim 28 ,wherein the near infrared fluorescent material is compatible with the resin.30. The method of producing a resin composition according to claim 28 ,wherein the content of the near-infrared fluorescent material in the resin composition is 0.001% by mass to 0.05% by mass.32. The method of producing a resin composition according to claim 20 ,wherein the radiopaque substance is one or more selected from the group consisting of barium sulfate, bismuth oxide, bismuth subcarbonate, calcium carbonate, aluminum hydroxide, tungsten, zinc oxide, zirconium oxide, zirconium, titanium, platinum, bismuth subnitrate, and bismuth.33. The method of producing a resin composition according to claim 20 ,wherein the content of the radiopaque substance in the mixture is 5% by mass to 50% by ...

CURABLE RESIN COMPOSITION

A curable resin composition, comprising a compound A represented by the following general formula (1): 2. The curable resin composition according to claim 1 , wherein X claim 1 , which the compound A has claim 1 , is a functional group having at least one hydrogen donor group selected from the group consisting of organic groups that have claim 1 , respectively claim 1 , a mercapto group claim 1 , an amino group claim 1 , an active methylene group claim 1 , a benzyl group claim 1 , a hydroxyl group claim 1 , and an ether bond.3. The curable resin composition according to claim 1 , wherein Rand R claim 1 , which the compound A has claim 1 , are each a hydrogen atom.4. The curable resin composition according to claim 1 , wherein the radical polymerization initiator B is at least one selected from the group consisting of thioxanthone-based photopolymerization initiators and benzophenone-based photopolymerization initiators.5. The curable resin composition according to claim 1 , wherein the radical polymerizable compound(s) C is/are a compound containing an ethylenically unsaturated double bond group.7. An adhesive resin composition for adhering a polarizer and a substrate to each other claim 1 , comprising a curable resin composition as recited in .8. A polarizing film claim 7 , comprising a polarizer claim 7 , and an adhesive layer positioned on/over at least one surface of the polarizer and yielded by curing an adhesive resin composition as recited in .9. The polarizing film according to claim 8 , wherein a transparent protective film is laid on/over the at least one surface of the polarizer to interpose the adhesive layer between the surface and the transparent protective film.10. An optical film claim 8 , on/over which at least one polarizing film as recited in is laminated.11. An image display device claim 8 , using a polarizing film as recited in . The present invention relates to a curable resin composition, in particular, a curable resin composition useful as an ...

POLY(BUTYLENE TEREPHTHALATE) METHOD AND ASSOCIATED COMPOSITION AND ARTICLE

A method for reducing outgassing of a polyester composed of repeat units derived from 1,4-butanediol is melt blending the polyester with 0.2 to 2 weight percent water, based on the weight of the polyester. In addition to water, the polyester can also be blended with 0.01 to 0.5 weight percent of a quencher. The method results in formation of a polyester composition which exhibits reduced outgassing, and is suitable for molding into articles, for example an automotive headlight reflector or bezel. 1. A method for reducing outgassing of a polyester having repeat units derived from 1 ,4-butanediol , comprising melt blending a polyester mixture comprising the polyester and 0.2 to 2 weight percent water , based on the weight of the polyester.2. The method of claim 1 , wherein the polyester mixture further comprises 0.01 to 0.5 weight percent claim 1 , based on the weight of the polyester claim 1 , of a quencher claim 1 , wherein the quencher is selected from the group consisting of phosphorous compounds claim 1 , boric acid claim 1 , aliphatic or aromatic carboxylic acids claim 1 , carboxylic acid anhydrides claim 1 , polyols claim 1 , epoxies claim 1 , or a combination thereof.4. The method of claim 1 , wherein the polyester mixture excludes quenchers claim 1 , wherein the quenchers are selected from the group consisting of phosphorous compounds claim 1 , boric acid claim 1 , aliphatic or aromatic carboxylic acids claim 1 , carboxylic acid anhydrides claim 1 , polyols claim 1 , epoxies claim 1 , or a combination thereof.5. The method of claim 3 , wherein the polyester mixture excludes quenchers selected from the group consisting of boric acid claim 3 , aliphatic or aromatic carboxylic acids claim 3 , carboxylic acid anhydrides claim 3 , polyols claim 3 , epoxies claim 3 , or a combination thereof.6. The method of claim 1 , wherein the polyester is selected from a poly(butylene terephthalate) claim 1 , a copolyetherester comprising a poly(butylene terephthalate) block ...

RESIN COMPOSITION AND MOLDED ARTICLE

The invention contains a resin and a near infrared fluorescent material which is one type or two or more types of compounds selected from General Formulas (I) to (I) and has a maximum fluorescence wavelength of 650 nm or longer. In Formulas, Rand R, Rand R, Rand R, and Rand Rform rings together with the nitrogen atom to which R, R, R, and Rare bonded; Rand Rrepresent a halogen atom or an oxygen atom; each of R, R, R, and Rindependently represents a halogen atom, a Calkyl group, a Calkoxy group, an aryl group, or a heteroaryl group; R, R, and Rrepresent a hydrogen atom or an electron withdrawing group; and each of Rand Rindependently represents a hydrogen atom, a halogen atom, a Calkyl group, a Calkoxy group, an aryl group, or a heteroaryl group. 112-. (canceled)14. The method of producing a resin composition according to claim 13 ,wherein the near infrared fluorescent material is compatible with the resin.15. The method of producing a resin composition according to claim 13 ,wherein the content of the near-infrared fluorescent material in the resin composition is 0.001% by mass to 0.05% by mass.16. The method of producing a resin composition according to claim 13 ,wherein the resin is a thermoplastic resin.17. The method of producing a resin composition according to claim 13 ,wherein the maximum fluorescence wavelength is 700 nm or longer.18. The method of producing a resin composition according to claim 16 , which is used as a medical material.19. The method of producing a resin composition according to claim 13 , comprising:further processing the resin composition to make a molded article which can be detected by light-emission.20. The method of producing a resin composition according to claim 19 ,wherein at least a part of the molded article is a medical tool that is used in the body of a patient. The present invention relates to a resin composition which emits near infrared fluorescent and a molded article obtained by processing the resin composition.A near ...

Benzoxaborole-Containing Coating Resistant To Cellulose-Supportable Fungus

A latex paint composition that contains a film-forming binder and pigment dispersed in an aqueous vehicle and also contains an effective amount of one or more cellulose-supportable fungus growth-inhibiting benzoxaborole compounds of Formula C is disclosed. A method of using that latex paint to inhibit the growth of a cellulose-supportable fungus on a cellulosic surface is also disclosed, as is a method of inhibiting such growth by painting over an fungus-infected surface with a contemplated latex paint. 3. The latex paint composition according to claim 2 , wherein X has a positive Hammett sigma value.5. The latex paint composition according to claim 1 , wherein said benzoxaborole is present in said latex paint composition in an amount of about 5 to about 2000 μg/mL.6Alternaria, Aspergillus, Aureobasidium, Rhizopus, Mucor, Penicillium, Cladosporium, Epicoccum, Chaetomium, Acremonium, Ulocladium, FusariumStachybotrys.. The latex paint composition according to claim 1 , wherein said cellulose-supportable fungus is selected from the group of genera consisting of one or more of and7. A method of inhibiting the growth of a cellulose-supportable fungus on a cellulosic surface free of visible fungus growth that comprises the step of coating said cellulosic surface that is free of visible fungus growth with a latex paint of .8. The method according to claim 1 , wherein said cellulosic surface is a paper-containing surface.9. The method according to claim 8 , wherein said paper-containing surface is one or more of those selected from the group consisting of drywall claim 8 , a cellulosic ceiling tile claim 8 , cardboard and wallpaper.10. The method according to claim 7 , wherein said paper-containing surface has one or more previously applied and dried coats of paint.11. The method according to claim 7 , wherein said paper-containing surface is free of previously applied and dried coats of paint.14. The method according to claim 7 , wherein said benzoxaborole is present in ...

PROCESS FOR MAKING A FABRICATED ARTICLE FROM POLYOLEFIN

The present disclosure describes a method for preparing a carbonized article comprising: providing an olefin resin in a melt phase; treating the olefin resin with a boron-containing species (BCS); forming a fabricated article from the treated olefin resin; crosslinking the fabricated article; stabilizing the fabricated article by air oxidation; and carbonizing the fabricated article. The present disclosure further describes a method for preparing a stabilized article. 1. A method for preparing a carbonized article comprising:(a) providing an olefin resin;(b) melt blending the olefin resin with a boron-containing species (BCS);(c) forming a fabricated article;(d) crosslinking the fabricated article;(e) stabilizing the fabricated article of step (d) by air oxidation; and(f) carbonizing the fabricated article of step (e).2. The method of claim 1 , wherein the BCS is a boron source suitable for depositing boron in the fabricated article.3. The method of claim 2 , wherein the boron source is an organoborane claim 2 , boric acid claim 2 , a derivative of boric acid claim 2 , a derivative of boronic acid claim 2 , a derivative of borinic acid claim 2 , a substituted borinic acid claim 2 , a derivative of borane claim 2 , a derivative of boronic ester claim 2 , a derivative of boroxine claim 2 , elemental boron a derivative of borazine claim 2 , a derivative of borohydride claim 2 , or a derivative of aminoborane.4. The method claim 1 , wherein step (d) comprises heating the fabricated article at or above 120° C.5. The method of claim 1 , wherein step (c) comprises converting said polyolefin resin to a fabricated article by fiber spinning claim 1 , film extrusion casting claim 1 , blown film processing claim 1 , profile extrusion through a die claim 1 , injection molding claim 1 , solution casting or compression molding.6. A method for preparing a stabilized article comprising:(c) providing an olefin resin;(d) melt blending the olefin resin with a boron-containing species ( ...

BORON-CONTAINING FABRICATED ARTICLE PREPARED FROM POLYOLEFIN PRECURSOR

In one instance, the present disclosure describes a crosslinked polyolefin article comprising: a carbon to hydrogen mol ratio of from 1:1.2 to 1:2.2; and 0.1 to 5 weight percent boron. In one instance, the present disclosure describes a stabilized polyolefin article comprising: a carbon to hydrogen mol ratio of from 1:0.8 to 1:1.3; greater than 18 weight percent oxygen; and 0.3 to 4 weight percent boron. 1. A crosslinked polyolefin article comprising:a carbon to hydrogen mol ratio of from 1:1.2 to 1:2.2; and0.1 to 5 weight percent boron.2. The crosslinked polyolefin article of claim 1 , wherein the carbon to hydrogen mol ratio is from 1:1.8 to 1:2.0.3. The crosslinked polyolefin article of claim 1 , wherein the carbon to hydrogen mol ration is from 1:1.8 to 1:2.2.4. The crosslinked polyolefin article of claim 1 , and having 0.5 to 5 weight percent boron.5. The crosslinked polyolefin article of claim 1 , and having 1.0 to 5 weight percent boron.6. The crosslinked polyolefin article of claim 1 , and having 2.0 to 5 weight percent boron.7. A stabilized polyolefin article comprising:a carbon to hydrogen mol ratio of from 1:0.8 to 1:1.3;greater than 18 weight percent oxygen; and0.3 to 4 weight percent boron.8. The stabilized polyolefin article of claim 7 , wherein the carbon to hydrogen mol ratio is from 1:0.8 to 1:1.0.9. The stabilized polyolefin article of claim 7 , wherein the carbon to hydrogen mol ratio is from 1:1.0 to 1:1.3.10. The stabilized polyolefin article of claim 7 , and having 1 to 4 weight percent boron.11. The stabilized polyolefin article of claim 7 , and having 2 to 4 weight percent boron.12. The stabilized polyolefin article of claim 7 , and having 3 to 4 weight percent boron.13. The stabilized polyolefin article of claim 7 , and having greater than 15 weight percent oxygen. Previously, carbonaceous articles, such as carbon fibers, have been produced primarily from polyacrylonitrile (PAN), pitch, or cellulose precursors. The process for making ...

PROCESS FOR MAKING A FABRICATED ARTICLE FROM POLYOLEFIN

A method for preparing a carbonized article comprising: (a) providing a polyolefin resin; (b) forming a fabricated article from the polyolefin resin; (c) crosslinking the fabricated article; (d) stabilizing the fabricated article in a boron-containing oxidizing environment (BOE); and (e) carbonizing the fabricated article. The present disclosure further describes a method for preparing a stabilized article. 1. A method for preparing a carbonized article comprising:(a) providing a polyolefin resin;(b) forming a fabricated article from the polyolefin resin;(c) crosslinking the fabricated article;(d) stabilizing the fabricated article in a boron-containing oxidizing environment (BOE); and(e) carbonizing the fabricated article.2. The method of claim 1 , wherein the BOE comprises air and a boron source.3. The method of claim 2 , wherein the boron source is a gaseous borate.4. The method of claim 3 , wherein the gaseous borate is trimethyl borate claim 3 , a derivative of boric acid claim 3 , a derivative of boronic acid claim 3 , a derivative of borinic acid claim 3 , a derivative of borane claim 3 , a derivative of boronic ester claim 3 , a derivative of or boroxine claim 3 , a derivative of borazine claim 3 , a derivative of borohydride or a derivative of aminoborane.5. The method of claim 1 , wherein step (d) comprises heating the crosslinked fabricated article at or above 120° C.6. The method of claim 1 , wherein step (b) comprises converting said polyolefin resin to a fabricated article by fiber spinning claim 1 , film extrusion casting claim 1 , blown film processing claim 1 , profile extrusion through a die claim 1 , injection molding claim 1 , solution casting or compression molding.7. A method for preparing a carbonized article comprising:(a) providing a crosslinked polyolefin fabricated article;(b) stabilizing the fabricated article in a boron-containing oxidizing environment (BOE); and(c) carbonizing the fabricated article.8. The method of claim 7 , wherein ...

METHOD FOR PRODUCING OXYMETHYLENE POLYMER AND OXYMETHYLENE POLYMER RESIN COMPOSITION

It has been desired to develop a method for producing an oxymethylene polymer, by which an oxymethylene polymer having a high polymerization degree can be produced with high efficiency while suppressing increase in the amount of generation of an odor. Further, it has been desired to develop an oxymethylene polymer resin composition, wherein generation of an odor at the time of molding or after molded to obtain a molded body is suppressed. The present invention provides a method for producing an oxymethylene polymer, wherein the oxymethylene polymer is produced by polymerizing a cyclic oligomer of formaldehyde, and wherein a boron trifluoride compound and an aryl fluoride boron compound are used as polymerization catalysts. The present invention also provides an oxymethylene polymer resin composition containing an oxymethylene polymer and a derivative of an aryl fluoride boron compound. 1. A method for producing an oxymethylene polymer , wherein the oxymethylene polymer is produced by polymerizing a cyclic oligomer of formaldehyde , and{'sub': ['3', 'n'], '#text': 'wherein a boron trifluoride compound (A) represented by BF.(X)(wherein n represents 0 or 1, and X represents an alkyl ether having 2 to 20 carbon atoms, tetrahydrofuran or phenol) and an aryl fluoride boron compound (B) are used as polymerization catalysts.'}2. The method for producing an oxymethylene polymer according to claim 1 , wherein said X is at least one selected from the group consisting of dimethyl ether claim 1 , diethyl ether and dibutyl ether.3. The method for producing an oxymethylene polymer according to claim 1 , wherein the aryl fluoride boron compound (B) is at least one selected from the group consisting of tris(pentafluorophenyl)borane claim 1 , bis(pentafluorophenyl)fluoroborane and pentafluorophenyldifluoroborane claim 1 , and hydrates thereof.4. The method for producing an oxymethylene polymer according to claim 1 , wherein the aryl fluoride boron compound (B) is used at a molar ...

POLYMERIZABLE COMPOSITION AND KIT, AND POLYMERIZATION INITIATOR

The present invention improves the long-term storage stability of a polymerizable composition including an organoborane and a polymerizable monomer. A polymerizable composition includes (A) an organoborane, (B) an acidic group-free polymerizable monomer, and (C) a stabilizer for the organoborane (A), the composition being such that when the composition, after being allowed to stand at 45° C. for 48 hours, is analyzed with an E-type viscometer at a temperature of 25° C. and a rotational speed of 50 rpm, the ratio of the viscosity after the standing to the viscosity before the standing (viscosity after standing/viscosity before standing) is less than 100. 1. A polymerizable composition comprising(A) an organoborane,(B) an acidic group-free polymerizable monomer, and(C) a stabilizer for the organoborane (A),the composition being such that when the composition, after being allowed to stand at 45° C. for 48 hours, is analyzed with an E-type viscometer at a temperature of 25° C. and a rotational speed of 50 rpm, the ratio of the viscosity after the standing to the viscosity before the standing (viscosity after standing/viscosity before standing) is less than 100.2. The polymerizable composition described in claim 1 , wherein the stabilizer (C) includes at least one selected from(C1) Lewis bases capable of forming a complex with the organoborane (A), and(C2) stabilizers other than (C1).3. The polymerizable composition described in claim 2 , wherein the stabilizers (C) include(C1) a Lewis base capable of forming a complex with the organoborane (A), and(C2) a stabilizer other than (C1).4. The polymerizable composition described in claim 2 , which comprises an organoborane-Lewis base complex formed from the organoborane (A) and the Lewis base (C1).5. The polymerizable composition described in claim 2 , wherein the stabilizer (C2) is at least one selected from(C2a) compounds which have a conjugated electron system, have a diketone structure, and have a hydrogen atom belonging ...

CURABLE COMPOSITIONS OF RESIN-LINEAR ORGANOSILOXANE BLOCK COPOLYMERS

Curable compositions of resin-linear organosiloxane block copolymers having improved shelf stability are disclosed. A stabilizer compound is added to the resin-linear organosiloxane block copolymer which increases the temperatures needed to effect final cure of the compositions. In other embodiments, the present disclosure provides curable compositions of resin linear organosiloxane block copolymers having improved physical properties, such as improved toughness. 1. A curable composition comprising: [{'sup': '1', 'sub': 2', '2/2, '40 to 90 mole percent disiloxy units of the formula [RSiO],'}, {'sup': '2', 'sub': '3/2', '10 to 60 mole percent trisiloxy units of the formula [RSiO],'}, '0.5 to 35 mole percent silanol groups [≡SiOH];', [{'sup': '1', 'sub': 1', '30, 'Ris independently a Cto Chydrocarbyl,'}, {'sup': '2', 'sub': 1', '20, 'Ris independently a Cto Chydrocarbyl;'}], 'wherein, [{'sup': 1', '1, 'sub': 2', '2/2', '2', '2/2, 'the disiloxy units [RSiO] are arranged in linear blocks having an average of from 10 to 400 disiloxy units [RSiO] per linear block,'}, {'sup': '2', 'sub': '3/2', 'the trisiloxy units [RSiO] are arranged in non-linear blocks having a molecular weight of at least 500 g/mol, and at least 30% of the non-linear blocks are crosslinked with each other, each linear block is linked to at least one non-linear block; and'}], 'wherein, {'sub': 'w', 'the organosiloxane block copolymer has a weight average molecular weight (M) of at least 20,000 g/mole; and'}], 'i) an organosiloxane block copolymer comprisingii) a stabilizer, wherein the stabilizer comprises alkaline earth metal salt, a metal chelate, a boron compound, a silicon-containing small-molecule or combinations thereof.2. (canceled)3. (canceled)4. The curable composition of claim 1 , wherein the boron compound comprises a boronic acid.5. (canceled)6. The curable composition of claim 4 , wherein the boronic acid comprises phenyl boronic acid.7. The curable composition of claim 1 , wherein the ...

COMPOSITION AND MOLDED BODY

The present invention provides a composition capable of reducing adhesion of biofilms and therefore useful for producing a molded body. 1. A composition comprising: at least one resin (A) selected from the group consisting of thermoplastic resins and thermosetting resins; and a quorum sensing inhibitor (B) ,wherein a common logarithm log S of solubility of the quorum sensing inhibitor (B) in water of 25° C. is less than 0.1, and{'sub': 1', '1, 'sup': '1/2', 'Rais greater than 3.2 MPa, provided that Rais a distance between a Hansen solubility parameter of the at least one resin (A) selected from the group consisting of thermoplastic resins and thermosetting resins and a Hansen solubility parameter of the quorum sensing inhibitor (B).'}2. The composition according to claim 1 , wherein the at least one resin (A) is a thermoplastic resin or thermoplastic resins.3. The composition according to claim 1 , further comprising an antimicrobial/antifungal agent (C).4. The composition according to claim 1 , further comprising a surface modifier (D).5. A molded body comprising the composition according to .6. The molded body according to claim 5 , wherein a dispersion force component γof a surface free energy is 25 mN/m or less claim 5 , or a sum of a dipole force component γand a hydrogen bonding component γof the surface free energy is 30 mN/m or more. The present invention relates to a composition and a molded body.Conventionally, resin molded bodies have been employed for home appliance members and the like. In order to prevent growth of microorganisms such as fungi, bacteria, and archaea on surfaces of the resin molded bodies, the resin molded bodies are mixed with an antimicrobial agent. For example, Patent Document 1 discloses a resin molded body including a silver-based antimicrobial agent.Patent Document 1: JP-A-2002-20632However, such a resin molded body including a silver-based antimicrobial agent is not capable of preventing, in environments in which water and an ...

Polymer compositions comprising cross-linked polymers comprising boronic ester functions enabling exchange reactions, process for preparing them and their use

The object of the invention is a polymer compositions comprising cross-linked polymer comprising boronic ester functions enabling exchange reactions, as well as free monofunctional boronic esters. The compositions are obtained from the modification of a polymer by a functionalised boronic ester additive. This polymer can be pre-functionalised boronic ester or functionalised on addition of the said additive. In particular, the invention relates to a process enabling the behaviour of a polymer to be modified by addition of a functional additive, enabling a cross-linked network containing exchangeable boronic ester links to be formed.

COMPOSITIONS CONTAINING BORANE OR CARBORANE CAGE COMPOUNDS AND RELATED APPLICATIONS

Compositions comprising a polymer-containing matrix and a filler comprising a cage compound selected from borane cage compounds, carborane cage compounds, metal complexes thereof, residues thereof, mixtures thereof, and/or agglomerations thereof, where the cage compound is not covalently bound to the matrix polymer. Methods of making and applications for using such compositions are also disclosed. 1. A nanocomposite composition comprising:a matrix comprising a polymer, wherein said polymer comprises less than 90 weight percent of a poly(conjugated diene), wherein said polymer comprises less than 90 weight percent of a polysiloxane; anda nanofiller comprising a mixture of agglomerations of cage compounds selected from the group consisting of a carborane cage compound, a metal complex thereof, and a residue thereof, wherein said cage compounds comprise at least 7 cage atoms,wherein said cage compounds are not covalently bound to said polymer, and wherein said nanocomposite has an increased or decreased glass transition temperature, storage modulus, loss modulus, thermal stability, or melt viscosity, as compared to said polymer.2. The composition of claim 1 , wherein said polymer comprises less than 10 weight percent of a poly(conjugated diene) claim 1 , wherein said polymer comprises less than 10 weight percent of a polysiloxane.3. The composition of claim 1 , wherein one of said cage compounds comprises a carborane cage compound having 12 cage atoms claim 1 , wherein said cage compound has an icosahedral structure.4. The composition of claim 1 , wherein one of said cage compounds comprises one or more pendant groups selected from the group consisting of a Cto Cn-alkyl claim 1 , a hydroxy claim 1 , a carboxy claim 1 , an epoxy claim 1 , an isocyanate claim 1 , a primary amine claim 1 , a silyl claim 1 , and an alkoxy silyl.5. The composition of claim 1 , wherein one of said cage compounds is selected from the group consisting of:{'sub': 2', 'n', 'n+2, '(a) a closo- ...

METHOD OF CROSSLINKING GLYCOSAMINOGLYCANS

A new hydrogel made of crosslinked glycosaminoglycans, particularly crosslinked hyaluronic acid, chondroitin or chondroitin sulfate, having reversible linkages using boronic acid or boroxole derivatives leading to new benefits. Glycosaminoglycans that are crosslinked via an alkoxyboronate ester anion formed between a diol portion of a diol-functional moiety grafted to a first glycosaminoglycan and a boronate hemiester grafted to a second glycosaminoglycan. 1. A fructose modified hyaluronic acid.3. Crosslinked hyaluronic acids , crosslinked via a phenylboronic acid crosslinker formed between a fructose moiety of a fructose modified hyaluronic acid and a phenylboronic acid grafted to a second hyaluronic acid.5. A method of crosslinking a first hyaluronic acid grafted with a fructose moiety and a second hyaluronic acid grafted with a phenylboronic acid , the method comprising crosslinking the first hyaluronic acid with the second hyaluronic acid by forming a phenylboronic acid crosslinker between the phenylboronic acid of the second hyaluronic acid and the fructose moiety of the first hyaluronic acid grafted with a fructose moiety.7. Crosslinked hyaluronic acids produced according to the method according to .8. Crosslinked hyaluronic acids produced according to the method according to .9. A polymer composition claim 3 , comprising crosslinked hyaluronic acids according to and an aqueous buffer.10. The polymer composition comprising crosslinked hyaluronic acids according to and an aqueous buffer. This application is a continuation application of U.S. Ser. No. 16/322,615 filed Feb. 1, 2019, which application is a U.S. National Stage of PCT/EP2017/069574, filed Aug. 2, 2017, which application claims priority under 35 U.S.C. § 119 of U.S. Provisional Application No. 62/370,479, filed Aug. 3, 2016; and European Patent Application No. 16206624.5, filed Dec. 23, 2016, each hereby expressly incorporated by reference in its entirety and each assigned to the assignee hereof.The ...

NEAR-INFRARED ABSORBING COMPOSITION, METHOD FOR PRODUCING DISPERSION LIQUID, FILM, OPTICAL FILTER, METHOD FOR FORMING PATTERN, LAMINATE, SOLID-STATE IMAGING ELEMENT, IMAGE DISPLAY DEVICE, AND INFRARED SENSOR

Provided are a near-infrared absorbing composition including a near-infrared absorbing pigment having an oxocarbon skeleton, a coloring agent derivative, a resin, and a solvent, in which the coloring agent derivative is a compound having a cation and an anion in a molecule, and the near-infrared absorbing composition contains 0.5 to 25 parts by mass of the coloring agent derivative with respect to 100 parts by mass of the near-infrared absorbing pigment; a method for producing a dispersion liquid; a film; an optical filter; a method for forming a pattern; a laminate; a solid-state imaging element; an image display device; and an infrared sensor. 1. A near-infrared absorbing composition comprising:a near-infrared absorbing pigment having an oxocarbon skeleton;a coloring agent derivative;a resin; anda solvent,wherein the coloring agent derivative is a compound having a cation and an anion in a molecule, andthe near-infrared absorbing composition contains 0.5 to 25 parts by mass of the coloring agent derivative with respect to 100 parts by mass of the near-infrared absorbing pigment.2. The near-infrared absorbing composition according to claim 1 ,wherein the near-infrared absorbing pigment has a maximum absorption wavelength in a range of 700 to 1200 nm.3. The near-infrared absorbing composition according to claim 1 ,wherein an absolute value of a difference between an amount of the near-infrared absorbing pigment dissolved in 100 g of propylene glycol methyl ether acetate at 25° C. and an amount of the coloring agent derivative dissolved in 100 g of propylene glycol methyl ether acetate at 25° C. is 10 g or less.15. The near-infrared absorbing composition according to claim 1 ,wherein the coloring agent derivative is a compound having at least one group selected from an acid group, a basic group, and a hydrogen-bonding group.16. The near-infrared absorbing composition according to claim 1 ,wherein the coloring agent derivative has at least one group selected from a ...

Urethane acrylate hybrid structure adhesives

A polymerizable adhesive composition comprising a two-part hybrid polymerizable adhesive composition is disclosed. In particular, the polymerizable adhesive composition comprises an organoborane monoamine complex, a free polyol comprising a dimer fatty polyol and a polyether polyol, at least one free radically polymerizable component, an isocyanate-terminated urethane pre-polymer, a free isocyanate and a low molecular weight chain extending compound. Also disclosed is methods of making and using a hybrid adhesive obtained from polymerization of the polymerizable adhesive composition

RESIN COMPOSITION

A resin composition containing (A) an epoxy resin; (B) a compound represented by formula (1) below; (C) a curing accelerator; and (D) a silane coupling agent is provided. The compound of the (B) component has a content of 1:0.5 to 1:2.5, in terms of an equivalent ratio between epoxy groups in the epoxy resin of the (A) component and thiol groups in the compound of the (B) component, the silane coupling agent of the (D) component has a content of 0.2 parts by mass to 50 parts by mass with respect to 100 parts by mass in total of the (A) component, the (B) component, the (C) component, and the (D) component, and an equivalent ratio between thiol groups in the compound of the (B) component and Si in the silane coupling agent of the (D) is 1:0.002 to 1:1. 2. The resin composition according to claim 1 , further comprising (E) a stabilizer.3. The resin composition according to claim 2 , wherein the stabilizer of the (E) component is at least one selected from the group consisting of liquid boric acid ester compounds claim 2 , aluminum chelate claim 2 , and barbituric acids.4. The resin composition according to claim 1 , wherein the silane coupling agent of the (D) component is at least one selected from the group consisting of 3-glycidoxypropyltrimethoxysilane claim 1 , 2-(3 claim 1 ,4-epoxycyclohexyl)ethyltrimethoxysilane claim 1 , 3-methacryloxypropyltrimethoxysilane claim 1 , and 8-glycidoxyoctyltrimethoxysilane.5. The resin composition according to claim 1 , wherein the curing accelerator of the (C) component is an imidazole-based curing accelerator claim 1 , a tertiary amine-based curing accelerator claim 1 , or a phosphorus compound-based curing accelerator.6. A one-component adhesive containing the resin composition according to .7. A cured resin obtained by heating the resin composition according to .8. An image sensor module manufactured with the one-component adhesive according to .9. An electronic component manufactured with the one-component adhesive according ...

RADIATION CURABLE COMPOSITIONS FOR ADDITIVE FABRICATION WITH IMPROVED TOUGHNESS AND HIGH TEMPERATURE RESISTANCE

Radiation curable compositions for additive fabrication with improved toughness are described and claimed. Such resins include a rubber toughenable base resin package and a liquid, phase-separating toughening agent. The rubber toughenable base resin, which may possess a suitably high average molecular weight between crosslinks and may be a pre-reacted hydrophobic macromolecule, may further include a cationically polymerizable component, a radically polymerizable component, a cationic photoinitiator, a free radical photoinitiator, and customary additives. Also described and claimed are methods for forming a three-dimensional objects using such radiation curable compositions for additive fabrication with improved toughness, along with the three-dimensional parts created therefrom. 1. A radiation curable composition for additive fabrication with improved toughness comprising: a cationically polymerizable component;', 'a radically polymerizable component;', 'a cationic photoinitiator;', 'a free radical photoinitiator; and', 'optionally, customary additives; and, 'a rubber toughenable base resin further comprising'}a liquid phase-separating toughening agent;wherein the liquid phase-separating toughening agent is present in an amount, relative to the weight of the rubber toughenable base resin, in a ratio from 1:99 to about 1:9, and{'sub': 'C', 'wherein the average molecular weight between crosslinks (M) of the rubber toughenable base resin is greater than 130 g/mol.'}2. The radiation curable composition for additive fabrication with improved toughness of claim 1 , wherein the liquid phase-separating toughening agent is a high molecular weight dimer fatty acid polyol.3. The radiation curable composition for additive fabrication with improved toughness of claim 1 , wherein the high molecular weight polyol is selected to be configured to form claim 1 , after curing of the radiation curable composition claim 1 , phase domains with an average size of from about 2 microns to ...

RADIATION-ACTIVATABLE PRESSURE-SENSITIVE ADHESIVE TAPE HAVING A DARK REACTION AND USE THEREOF

A pressure-sensitive adhesive tape comprising or consisting of a radiation-activatable polymerizable composition comprising or consisting of: 1. An adhesive tape which is pressure sensitive at room temperature and comprises or consists of a radiation-activatable polymerizable composition comprising or consisting of:A 5 to 60 parts by weight of at least one film former component;B 40 to 95 parts by weight of at least one epoxy component;C 0.1 to 10 parts by weight of at least one photoinitiator, andD optionally 0.1 to 200 parts by weight of at least one additive,based in each case on the radiation-activatable polymerizable composition, where the parts by weight of components A and B add up to 100, whereinthe film former component A comprises or consists of at least one polyurethane polymer.2. The adhesive tape as claimed in claim 1 , wherein the polyurethane polymer of the film former component A has a weight-average molecular weight Mof at least 40 000 g/mol claim 1 , determined via GPC at 25° C. with polystyrene as standard claim 1 , THF/0.1% by volume of trifluoroacetic acid as eluent claim 1 , sample concentration 4 g/L claim 1 , flow rate 1.0 mL/min.3. The adhesive tape as claimed in claim 1 , wherein polyurethane polymer of the film former component A is a linear polyurethane polymer.4. The adhesive tape as claimed in claim 1 , wherein the polyurethane polymer of the film former component A is an OH-functional polyurethane polymer.5. The adhesive tape as claimed in claim 1 , wherein the epoxy component B contains at least 10% by weight of epoxy resins that are liquid at 25° C. claim 1 , based on the epoxy component B.6. The adhesive tape as claimed in claim 1 , wherein the epoxy component B contains not more than 60% by weight of epoxycyclohexyl-based epoxy resins claim 1 , based on the epoxy component B.7. The adhesive tape as claimed in claim 1 , wherein the epoxy component B has an average functionality based on the epoxy groups of at least 1.5 to 6.0.8. The ...

HANDLING ADDITIVE FOR SILICONE ELASTOMER BASES

A handling additive composition is disclosed. The composition is useful to improve handling of silicone elastomers prepared from polydiorganosiloxanes and silicone elastomers made therewith. 1. A handling additive composition comprising:at least one boric acid derivative selected from the group consisting of borinic acids, boronic acids, and mixtures thereof;a silicone polymer; andoptionally, a powder.2. The handling composition of claim 1 , wherein the boric acid derivative is selected from the group consisting of phenylboronic acid claim 1 , 4-fluorophenylboronic acid claim 1 , 3 claim 1 ,4-difluorophenylboronic acid claim 1 , 3 claim 1 ,4 claim 1 ,5-trifluorophenylboronic acid claim 1 , n-butylboronic acid claim 1 , 2-thienylboronic acid claim 1 , 1 claim 1 ,4-phenylenediboronic acid claim 1 , bis(pentafluorophenyl)borinic acid claim 1 , diphenylborinic acid claim 1 , dimesitylborinic acid claim 1 , Bis(3 claim 1 ,4-dimethylphenyl)borinic acid claim 1 , borinic Acid claim 1 , B claim 1 ,B-Bis(2 claim 1 ,3 claim 1 ,4 claim 1 ,5 claim 1 ,6-pentafluorophenyl) claim 1 , and mixtures thereof.3. The handling composition of claim 1 , wherein the silicone polymer is selected from the group consisting of polydimethylsiloxanes claim 1 , alkylmethylpolysiloxanes claim 1 , alkylarylpolysiloxanes claim 1 , hydroxyfunctional siloxanes claim 1 , alkoxyfunctional siloxanes claim 1 , and mixtures thereof.4. The handling composition of claim 1 , wherein the powder is present and selected from the group consisting of polytetrafluoroethylene claim 1 , fumed silica claim 1 , carbon black claim 1 , carbon nanotubes claim 1 , multiwalled carbon nanotubes claim 1 , carbon fibres claim 1 , graphene claim 1 , nano diamond claim 1 , nano clay claim 1 , graphite claim 1 , polysaccharide nano compounds claim 1 , nano cellulose claim 1 , cellulose nano whiskers claim 1 , layered silicates claim 1 , boehmite claim 1 , hydroxyapatite fillers claim 1 , reinforcing fibres claim 1 , nylon claim 1 ...

METHOD FOR SURFACE MODIFICATION OF FLUORORESIN

To provide a method for surface modification of a fluororesin, that enables graft polymerization at a lower temperature than a conventional method. 1. A method for surface modification of a fluororesin , which comprises reacting a fluororesin with a radical reactive compound in the presence of an organometallic compound.2. The method for surface modification of a fluororesin according to claim 1 , wherein the fluororesin is in a film form or a particle form.3. The method for surface modification of a fluororesin according to claim 1 , wherein the fluororesin is at least one type selected from the group consisting of a ethylene-tetrafluoroethylene copolymer claim 1 , a perfluoro(alkyl vinyl ether)-tetrafluoroethylene copolymer claim 1 , a vinylidene fluoride polymer claim 1 , a vinyl fluoride polymer claim 1 , a vinylidene fluoride-hexafluoropropylene copolymer claim 1 , a tetrafluoroethylene-hexafluoropropylene-vinylidene fluoride copolymer claim 1 , a tetrafluoroethylene-propylene copolymer claim 1 , a tetrafluoroethylene-vinylidene fluoride-propylene copolymer claim 1 , a hexafluoropropylene-tetrafluoroethylene copolymer claim 1 , an ethylene-hexafluoropropylene-tetrafluoroethylene copolymer claim 1 , a chlorotrifluoroethylene polymer claim 1 , an ethylene-chlorotrifluoroethylene copolymer claim 1 , a polytetrafluoroethylene and a propylene-chlorotrifluoroethylene copolymer.4. The method for surface modification of a fluororesin according to claim 1 , wherein the organometallic compound contains at least one element selected from the group consisting of Group 12 elements claim 1 , Group 13 elements and Group 15 elements.5. The method for surface modification of a fluororesin according to claim 1 , wherein the organometallic compound is at least one type selected from the group consisting of a dialkyl zinc complex and a trialkylborane.6. The method for surface modification of a fluororesin according to claim 1 , wherein the organometallic compound is at least one ...

MONOMER MIXTURES FOR FORMING SILICON HYDROGELS

A polymerizable monomer mixture containing one or more silicon-containing biomedical device-forming monomers and a diluent; wherein the diluent comprises a boric acid ester of a monohydric alcohol is disclosed. 1. A polymerizable monomer mixture comprising one or more silicon-containing biomedical device-forming monomers and a diluent; wherein the diluent comprises a boric acid ester of a monohydric alcohol.2. The polymerizable monomer mixture of claim 1 , wherein the silicon-containing biomedical device-forming monomer is a silicon-containing monomer containing one or more Si—O units.3. The polymerizable monomer mixture of claim 1 , further comprising a hydrophilic monomer claim 1 , hydrophobic monomer or both.4. The polymerizable monomer mixture of claim 3 , wherein the hydrophilic monomer is selected from the group consisting of an unsaturated carboxylic acid claim 3 , vinyl lactam claim 3 , acrylamide claim 3 , polymerizable amine claim 3 , vinyl carbonate claim 3 , vinyl carbamate claim 3 , oxazolone monomer and mixtures thereof.5. The polymerizable monomer mixture of claim 3 , wherein the hydrophilic monomer is selected from the group consisting of methacrylic and acrylic acids claim 3 , 2-hydroxyethylmethacrylate claim 3 , N-vinylpyrrolidone claim 3 , methacrylamide claim 3 , N claim 3 ,N-dimethylacrylamide and mixtures thereof.6. The polymerizable monomer mixture of claim 3 , wherein the hydrophobic monomer is selected from the groups consisting of an ethylenically unsaturated polymerizable fluorine-containing monomer claim 3 , ethylenically unsaturated polymerizable fatty acid ester-containing monomer claim 3 , ethylenically unsaturated polymerizable polysiloxanylalkyl-containing monomer claim 3 , ethylenically unsaturated polymerizable monomer having ring-opening reactive functionalities claim 3 , and mixtures thereof.7. The polymerizable monomer mixture of claim 3 , wherein the hydrophobic monomer is selected from the groups consisting of an ethylenically ...

RESIN COMPOSITION CONTAINING ETHYLENE-VINYL ALCOHOL COPOLYMER

The present invention provides a resin composition containing (A) an ethylene-vinyl alcohol copolymer and (B) an unsaturated aldehyde (B), in which the content of the unsaturated aldehyde (B) with respect to the resin composition containing the ethylene-vinyl alcohol copolymer is 0.01 ppm or more and 100 ppm or less. The unsaturated aldehyde (B) is preferably crotonaldehyde, 2,4-hexadienal, 2,4,6-octatrienal or a combination thereof. In addition, it is preferred that the resin composition further contains a boron compound, and the content of the boron compound is 100 ppm or more and 5,000 ppm or less. Also, it is preferred that the resin composition further contains a conjugated polyene compound, and the content of the conjugated polyene compound is 0.01 ppm or more and 1,000 ppm or less. 1. A resin composition , comprising:(A) an ethylene-vinyl alcohol copolymer; and(B) an unsaturated aldehyde,wherein a content of the unsaturated aldehyde (B) with respect to the resin composition comprising the ethylene-vinyl alcohol copolymer is 0.01 ppm or more and 100 ppm or less.2. The resin composition according to claim 1 , wherein the unsaturated aldehyde (B) is (B-1) an unsaturated aliphatic aldehyde.3. The resin composition according to claim 2 , wherein the unsaturated aldehyde (B) is crotonaldehyde claim 2 , 2 claim 2 ,4-hexadienal claim 2 , 2 claim 2 ,4 claim 2 ,6-octatrienal or a combination thereof.4. The resin composition according to claim 1 , further comprising a boron compound claim 1 , wherein a content of the boron compound is 100 ppm or more and 5 claim 1 ,000 ppm or less.5. The resin composition according to claim 1 , further comprising a conjugated polyene compound claim 1 , wherein a content of the conjugated polyene compound is 0.01 ppm or more and 1 claim 1 ,000 ppm or less.6. The resin composition according to claim 5 , wherein the conjugated polyene compound is sorbic acid claim 5 , a sorbic acid salt or a combination thereof.7. The resin composition ...

COMPOSITE PARTICLES, KIT, MATERIAL, AND METHOD FOR PRODUCING COMPOSITE PARTICLES

The present invention improves the long-term storage stability of an organoborane-Lewis base complex. First composite particles of the present invention include particles of an organic polymer (B), and an organoborane-Lewis base complex (A) contained in the particles. Second composite particles of the present invention include particles of an inorganic compound (B′), and an organoborane-Lewis base complex (A) adsorbed on the particles. 1. Composite particles comprising:component (B′): particles of an inorganic compound; andcomponent (A): an organoborane-Lewis base complex adsorbed on the component (B′).2. The composite particles according to claim 1 , [{'sub': '3', 'a compound represented by BR, wherein each R is independently an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, a saturated or unsaturated alicyclic group having 3 to 20 carbon atoms, or an alkoxy group having 1 to 20 carbon atoms, and two or more of the groups R may be bonded to each other to form a ring; and'}, {'sub': '3', 'a partial oxide of the compound represented by BR.'}], 'wherein an organoborane of the component (A) is at least one selected from3. The composite particles according to claim 1 ,wherein a Lewis base of the component (A) is at least one selected from an amine, an amidine, a hydroxide, and an alkoxide.4. The composite particles according to claim 1 ,{'sup': 1', '2', '1', '2, 'sub': m', '2-m', 'n', '3-n, 'wherein the component (A) is a compound represented by (N(R)(H)RO)BR, wherein Ris an alkyl group having 1 to 20 carbon atoms, Ris an alkylene group having 1 to 20 carbon atoms, R is an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, a saturated or unsaturated alicyclic group having 3 to 20 carbon atoms, or an alkoxy group having 1 to 20 carbon atoms, two of the groups R may be bonded to each other to form a ring, m is 1 or 2, and n is 1 or 2.'}5. The composite particles according to claim 1 ,{'sub': x', 'y', 'z ...

Thermally initiated acid catalyzed reaction between silyl hydride and siloxane

A composition contains a mixture of silyl hydride, a siloxane, a Lewis acid catalyst and an amine having the following formula: R 1 R 2 R 3 N; where the nitrogen is not a member of an N═C—N linkage and where each of R 1 , R 2 , and R 3 is independently selected from a group consisting of hydrogen, alkyl, substituted alkyl, and conjugated moieties; and wherein at least one of R 1 , R 2 and R 3 is a conjugated moiety connected to the nitrogen by a conjugated carbon.

ELECTROCHROMIC DEVICE

Disclosed are curved electrochromic devices comprising an electrochromic apparatus disposed between first and second curved layers of transparent material, and the first and second curved layers have exterior and inner surfaces, wherein the inner surfaces face the electrochromic apparatus. Also disclosed are processes for manufacturing the disclosed bubble visors. 1. An electrochromic device having a layer of transparent polymeric material connected to an electrochromic apparatus , wherein the transparent polymeric material comprisesa coating opposite the electrochromic apparatus and that is capable of reflecting infrared and ultraviolet wavelength radiation;a coating opposite the electrochromic apparatus and blocks wavelengths of visible radiation capable of initiating chemical decomposition of an electrochromic compound; ora dielectric coating capable of transmitting light within the range of about 400 nm to 700 nm.2. An electrochromic device according to claim 1 , wherein the transparent polymeric material is a thermoplastic polymer.3. An electrochromic device according to claim 1 , wherein the electrochromic apparatus comprises an electrolyte membrane comprising a non-aqueous electrolyte and a polymer claim 1 , and the electrolyte membrane has a membrane first surface and a membrane second surface.4. An electrochromic device according to claim 3 , wherein the non-aqueous electrolyte is an ionic liquid.5. An electrochromic device according to claim 4 , wherein the ionic liquid comprises an anion selected from the group consisting of sulfates claim 4 , alkylsulfates claim 4 , arylsulfates claim 4 , alkylsulfonates claim 4 , fluorinated alkylsulfates claim 4 , fluorinated alkylsulfonates claim 4 , fluoroalkylsulfonylimides claim 4 , hexafluorophosphate claim 4 , tetracyanoborate claim 4 , tetrafluoroborate claim 4 , thiocyanate claim 4 , thiosalicylate claim 4 , dicyanamide claim 4 , and halides.6. An electrochromic device according to claim 4 , wherein the ionic ...

Composition

A composition having excellent adhesiveness to poorly adhesive materials such as polyolefins is provided. The solution is a composition comprising the following (1) to (2): (1) (meth)acrylates containing the following (1-1) to (1-3): (1-1) a (meth)acrylate having a hydroxyl group, (1-2) an alkyl (meth)acrylate, and (1-3) a (meth)acrylate having a cyclic ether skeleton, and (2) an organoboron compound. The content ratio of (1-1), (1-2), and (1-3) is (1-1):(1-2):(1-3)=(10 to 90):(5 to 80):(5 to 80) in mass ratio in 100 parts by mass of (1) (meth)acrylates.

COMPOSITION, FILM, NEAR INFRARED CUT FILTER, LAMINATE, PATTERN FORMING METHOD, SOLID IMAGE PICKUP ELEMENT, IMAGE DISPLAY DEVICE, INFRARED SENSOR, AND COLOR FILTER

A composition includes two or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C., in which the two or more near infrared absorbing compounds include a first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, and a second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, and a difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm. 1. A composition comprising:three or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C.,wherein at least three of the three or more near infrared absorbing compounds are each independently selected from the group consisting of a pyrrolopyrrole compound, a squarylium compound, a phthalocyanine compound, a naphthalocyanine compound, and a rylene compound, andwherein the three or more near infrared absorbing compounds includea first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, anda second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, anda difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm.2. The composition according to claim 1 ,wherein in each of the first near infrared absorbing compound and the second near infrared absorbing compound, a ratio A1/A2 of an ...

Pneumatic Tire

A pneumatic tire includes a belt layer and a carcass layer. A rubber composition for belts, constituting the belt layer, contains, per 100 parts by mass of a diene rubber containing a natural rubber, from 0.3 to 1.5 parts by mass of cobalt borate neodecanoate and from 4.5 to 7.0 parts by mass of sulfur. The dynamic storage modulus at 20° C. of the rubber composition for belts is from 13 to 18 MPa, and a ratio of a 100% tensile stress of the rubber composition for belts to a 100% tensile stress of a rubber composition for carcasses, constituting the carcass layer is from 1.5 to 2.5. 1. A pneumatic tire comprising a belt layer and a carcass layer , whereina rubber composition for belts constituting the belt layer contains: per 100 parts by mass of a diene rubber containing a natural rubber, from 0.3 to 1.5 parts by mass of cobalt borate neodecanoate and from 4.5 to 7.0 parts by mass of sulfur,a dynamic storage modulus (E′) at 20° C. of the rubber composition for belts is from 13 to 18 MPa, anda ratio (MB/MC) of a 100% tensile stress (MB) of the rubber composition for belts to a 100% tensile stress of a rubber composition for carcasses, constituting the carcass layer, (MC) is from 1.5 to 2.5.2. The pneumatic tire according to claim 1 , wherein the rubber composition for carcasses contains SC parts by mass of sulfur per 100 parts by mass of a diene rubber claim 1 , the rubber composition for belts contains SB parts by mass of the sulfur claim 1 , and a ratio (SB/SC) of the compounded content of the sulfur of the rubber composition for belts (SB) to the compounded content of the sulfur of the rubber composition for carcasses (SC) is from 2.0 to 3.0.3. The pneumatic tire according to claim 1 , wherein the rubber composition for belts contains claim 1 , per 100 parts by mass of the diene rubber claim 1 , 0.5 parts by mass or greater but less than 3.0 parts by mass of a phenol-based resin and from 0.5 to 5.0 parts by mass of a curing agent.4. The pneumatic tire according to ...

METHOD TO IMPROVE THE SURFACE MODIFICATION BY USING ALKYLBORANES

Process for the modification of a surface of a solid substrate comprising treatment of the surface with (i) a solution comprising an organoborane-amine complex and a polymer and subsequently with (ii) a polymerizable compound (herein referred to as “monomer”) and optionally a deblocking agent 1. A process for modifying surface of a solid substrate , the process comprising treating the surface with(i) a solution comprising an organoborane-amine complex and a polymer and, subsequently,(ii) a polymerizable compound and, optionally, a deblocking agent.2. The process of claim 1 , wherein the organoborane-amine complex has a structure of formula (I){'br': None, 'sub': 1', '2', '3', '4', '5', '6, 'RRRB—NRRR\u2003\u2003(1),'}{'sub': 1', '2', '3', '1', '2', '3, 'wherein R, Rand Rare each independently an alkyl group, a cycloalkyl group, an alkyl or cycloalkyl group substituted with a heteroatom, an alkylamino group, an aryl group, a heteroaryl group, an alkoxy group or an aryloxy group, with the proviso that at least one of R, Rand Ris an alkyl or aryl group, and'}{'sub': 4', '5', '6', '4', '5', '6, 'R, Rand Rare each independently hydrogen, an alkyl group, a cycloalkyl group, a substituted alkyl group, an alkoxy group, an alkylamino group, an aryl group or a heteroaryl group, with the proviso that not more than two of R, Rand Rare simultaneously hydrogen, or'}{'sub': 4', '5', '6, 'NRRRis a heterocyclic aliphatic or aromatic amine, optionally comprising at least one heteroatom selected from the group consisting of N, O, S and P.'}3. The process of claim 1 , wherein the organoborane-amine complex is a trialkylborane-amine complex.4. The process of claim 1 , wherein the polymer is a polyalkylenoxide claim 1 , a polyalkyleneglycol claim 1 , a polycaprolactone claim 1 , a polyvinyllactone claim 1 , a polyvinyllactame or a mixture thereof.5. The process of claim 1 , wherein the polymer is a polyethyleneglycol or a polyvinylpyrrollidone.6. The process of claim 1 , wherein the ...

Laminate And Method Of Preventing Or Reducing Electrification Of The Same

To provide a laminate comprising a substrate and a cured silicone product, wherein the substrate and the cured silicone product are integrated well and the cured silicone product provides superior electrification preventing or reducing properties to the laminate. A laminate comprising: a substrate (L1), a primer layer (L2) formed on the substrate (L1), and a cured silicone layer (L3) including a lithium salt (a) and a polyether modified polysiloxane (b), which is formed on the primer layer (L2). The laminate can be used for a releasable or adhesive film.

POLYMERIC FILM COMPOSITION FOR NON-ENZYMATIC GLUCOSE SENSOR AND NON-ENZYMATIC GLUCOSE SENSOR INCLUDING THE SAME

A polymeric film composition and a non-enzymatic glucose sensor including the functional polymeric film are provided. The polymeric film composition includes polyurethane and perfluorosulfonic acid polymer. 1. A polymeric film composition for a non-enzymatic glucose sensor comprising polyurethane and perfluorosulfonic acid polymer.2. The polymeric film composition of claim 1 , further comprising amino phenyl boronic acid.3. The polymeric film composition of claim 1 , wherein an amount of the polyurethane and perfluorosulfonic acid polymer is 1.0 wt % to 5.0 wt % with respect to a total weight of the polymeric film composition.4. The polymeric film composition of claim 2 , wherein the amino phenyl boronic acid is included in an amount of 0.05 wt % to 0.3 wt % with respect to a total weight of the polymeric film composition.5. A non-enzymatic glucose sensor comprising:a reference electrode;a working electrode electrically connected to the reference electrode; anda polymeric film provided on a surface of the working electrode,wherein the polymeric film comprises polyurethane and perfluorosulfonic acid polymer.6. The non-enzymatic glucose sensor of claim 5 , wherein a surface of the working electrode comprises a single metal or an alloy of a plurality of metals.7. The non-enzymatic glucose sensor of claim 6 , wherein the single metal or an alloy of a plurality of metals on the surface of the working electrode comprises any one single metal or an alloy of two or more of the single metals selected from the group consisting of Cu claim 6 , Au claim 6 , Zn claim 6 , Mn claim 6 , Ni claim 6 , and Co.8. The non-enzymatic glucose sensor of claim 7 , wherein the surface of the working electrode comprises a Cu—Co alloy.9. The non-enzymatic glucose sensor of claim 8 , wherein within the Cu—Co alloy claim 8 , the atomic percentage of Cu is from 45-65% and the atomic percentage of Co is from 35-55%.10. The non-enzymatic glucose sensor of claim 5 , wherein the working electrode is a ...

LIQUID, HYBRID UV/VIS RADIATION CURABLE RESIN COMPOSITIONS FOR ADDITIVE FABRICATION

Liquid radiation curable compositions are disclosed which are suitable for hybrid (i.e. cationic and free-radical) polymerization when processed via additive fabrication equipment utilizing sources of actinic radiation with peak spectral intensities in the UV/vis region. According to one aspect, the compositions possess a first photoinitiator that is an iodonium salt of a non-fluorinated borate anion. According to another aspect, the composition is substantially devoid of a Norrish Type I and/or Type II photoinitiator. Also disclosed are methods of creating three-dimensional parts via additive fabrication processes utilizing sources of actinic radiation with peak spectral intensities in the UV/vis region employing liquid radiation curable compositions suitable for hybrid polymerization, and the parts cured therefrom. 1. A radiation curable composition comprising a cationically curable constituent and a free-radically curable constituent , said composition further comprising at least a first photoinitiator that is an iodonium salt of a non-fluorinated borate anion.2. The radiation curable composition of claim 1 , wherein the iodonium salt of the non-fluorinated borate anion is an iodonium salt of a non-halogenated borate anion.4. The radiation curable composition of claim 3 , wherein R-Rare independently selected from an aryl radical claim 3 , optionally substituted at one or more substitutable carbon atoms with alkyl or alkoxy.5. The radiation curable composition of claim 4 , wherein R-Rare each phenyl claim 4 , optionally independently substituted with alkyl or alkoxy claim 4 , wherein alkyl or the alkyl portion of alkoxy has from 1-10 carbon atoms.7. The radiation curable composition of claim 1 , wherein the iodonium salt of the non-fluorinated borate anion has a diaryliodonium cation.8. The radiation curable composition of claim 7 , wherein the diaryliodonium cation of the iodonium salt is a diphenyliodonium salt claim 7 , having two phenyl radicals optionally ...

Functionalized Polymer, Process For Preparing And Rubber Compositions Containing The Functionalized Polymer

Disclosed herein are a functionalized diene monomer-containing polymer containing first and second functionalizing groups, processes for preparing the functionalized polymer, and rubber compositions containing the functionalized polymer. The functionalized polymer contains polymer chains comprises of at least one conjugated diene monomer optionally in combination with at least one vinyl aromatic monomer wherein each polymer chain is functionalized at its chain end with at least the first functionalizing group and is coupled via the first functionalizing group to the second functionalizing group.

POLYMER-CONTAINING COMPOSITION AND ANTIFOULING COATING COMPOSITION

Provided is an antifouling coating composition, which can form a coating film having good hardness and good physical properties and having a wear degree appropriate for expressing a long-term antifouling effect, has a viscosity not being excessively high, and makes it possible to reduce a content of volatile organic compounds, and a polymer-containing composition which is suitable for obtaining the antifouling coating composition. The polymer-containing composition contains a (meth)acryl-based copolymer (A-1), in which the (meth)acryl-based copolymer (A-1) contains a constitutional unit (U11) or a constitutional unit (U12) having carboxylate forming an ionic bond with a divalent metal atom, and has a weight-average molecular weight of 1,000 to 5,000, and the polymer-containing composition has a coating film hardness (Martens hardness) equal to or higher than 2.5 N/mm. 121-. (canceled)22. A polymer-containing composition comprising:a (meth)acryl-based copolymer (A-1),wherein the (meth)acryl-based copolymer (A-1) contains a constitutional unit (U11) represented by Formula (11), a constitutional unit (U12) represented by Formula (12), or both, and has a weight-average molecular weight of 1,000 to 5,000, andthe (meth)acryl-based copolymer (A-1) contains a constitutional unit (U3) in addition to the constitutional unit (U11), the constitutional unit (U12), or both, andthe constitutional unit (U3) contains a constitutional unit derived from a monomer (u3-1) having a substituted or unsubstituted alicyclic functional group,{'sup': '2', 'claim-text': [{'br': None, '—(C═O)—O-M-O—(C═O)—\u2003\u2003(11)'}, {'br': None, 'sup': '32', '—(C═O)—O-M-R\u2003\u2003(12)'}], 'wherein a coating film hardness of the polymer-containing composition is equal to or higher than 2.5 N/mm,'}{'sup': '32', 'wherein Rrepresents an organic acid residue, and M represents a divalent metal atom.'}23. The polymer-containing composition according to claim 22 ,wherein the monomer (u3-1) having a ...

Epoxy resin composition, prepreg, and fiber-reinforced composite material

The present invention aims to provide an epoxy resin composition that is high in both fast curability and storage stability, a prepreg prepared by using the epoxy resin composition, and a fiber reinforced composite material prepared by curing the prepreg. The epoxy resin composition contains the following components [A], [B], [C], and [D] and meets the following requirements [a], [b], and [c]: [A]: epoxy resin, [B]: dicyandiamide, [C]: aromatic urea, [D]: borate ester, [a]: 0.014≤(content of component [D]/content of component [C])≤0.045, [b]: 0.9≤(number of moles of active groups in component [A]/number of moles of active hydrogen in component [B])≤1.2, and [c]: 14≤(content of component [A]/content of component [C])≤25.

Photocontrolled dynamic covalent linkers for polymer networks

Reversibly crosslinkable polymeric networks, including reversibly crosslinkable hydrogel networks are provided. Also provided are methods of making the polymeric networks and methods of using the hydrogel networks in tissue engineering applications. The reversibly crosslinkable polymeric networks are composed of polymer chains that are covalently crosslinked by azobenzene boronic ester bonds that can be reversibly formed and broken by exposing the polymeric networks to different wavelengths of light.

BONDING COMPOSITION AND COMPONENT THEREOF, AND METHOD OF USING THE SAME

A two-part bonding composition includes parts A and B. Part A includes an organoborane-base complex and reactive diluent. Reactive diluent includes: triallyl isocyanurate; triallyl cyanurate; N-allylamide having the formula RC(=0)N(R) CHCH═CH, wherein Rand Rindependently represent alkyl groups having from 1 to 7 carbon atoms, optionally interrupted up to 3 times by oxygen, and optionally substituted up to 2 times with hydroxyl groups, or taken together Rand Rrepresent —(CH)—, —(CH)—, or —(CH)—; and/or allyl ether having the formula R[OCHCH═CH]n wherein Rrepresents an n-valent hydrocarbonaceous group having from 1 to 24 carbon atoms, optionally interrupted up to 8 times by oxygen, and optionally substituted up to 6 times with hydroxyl groups, and n represents 1, 2, 3, 4, 5, or 6. Part B includes free-radically polymerizable monomer and at least one compound capable of decomplexing the organoborane-base complex. A method combining Parts A and B is also disclosed. 2. The two-part bonding composition of claim 1 , wherein the at least one reactive diluent comprises triallyl isocyanurate.3. The two-part bonding composition of claim 1 , wherein the at least one reactive diluent comprises triallyl cyanurate.4. The two-part bonding composition of claim 1 , wherein the at least one reactive diluent comprises at least one of N-allylpyrrolidone claim 1 , N-allylvalerolactam claim 1 , or N-allylcaprolactam.5. The two-part bonding composition of claim 1 , wherein the at least one reactive diluent comprises the allyl ether.6. The two-part bonding composition of claim 5 , wherein the allyl ether comprises at least one of phenyl allyl ether claim 5 , trimethylolpropane diallyl ether claim 5 , or pentaerythritol tetraallyl ether.7. The two-part bonding composition of claim 1 , wherein the at least one compound capable of decomplexing the organoborane-base complex comprises at least one of a carboxylic acid or an acid anhydride.9. The two-part bonding composition of claim 8 , wherein ...

One component (1k) composition based on epoxy resin

The present invention is directed to an one-component (1K) composition comprising, based on the weight of the composition:from 30 to 90 wt. % of a) at least one epoxy resin;from 1 to 50 wt. % of b) at least one mercapto compound having at least two mercapto groups reactive towards epoxide;from 0.5 to 25 wt. % of c) at least one organoboron compound selected from tetrasubstituted borate salts of monovalent cations of tertiary amines; and,from 0.5 to 25 wt. % of d) at least one (meth)acrylamide monomer of Formula (VII):wherein: Ra is H or Me;G is selected from —NH2, —NHRb and —N(Rb)(Rc);Rb and Rc are independently selected from C1-C18 alkyl, C1-C18 hydroxyalkyl, C1-C18 alkalkoxy, C6-C18 aryl and —(CH2)n—N(Rd)(Re);n is an integer of from 1 to 4; and,Rd and Re are independently selected from H and C1-C6 alkyl.

CURE-ON-DEMAND AND TIME-LAPSE POLYMERIZATION

The present invention provides compositions, methods and kits for the temporal control induction time for a polymerization reaction. 1. A composition for forming a polymer comprising a polyhydroxy monomer , and a borate ion source; or an epoxy resin and a compound comprising one or more thiol groups.2. The composition of claim 1 , wherein the composition further comprises urea and at least one urease source.3. The composition of claim 1 , wherein the polyhydroxy monomer is selected from the group consisting of poly(vinyl) alcohol (PVA) claim 1 , 1 claim 1 ,4-butanediol claim 1 , 1 claim 1 ,6-hexanediol claim 1 , ethylene glycol claim 1 , 2-ethyl-1 claim 1 ,3-hexanediol (EHD) claim 1 , 2-butyl-2-ethyl-1 claim 1 ,3-propanediol (BEPG) claim 1 , 2 claim 1 ,2 claim 1 ,4-trimethyl-1 claim 1 ,3-pentanediol (TMPD) claim 1 , 2 claim 1 ,4-deithyl-1 claim 1 ,5-pentanediol (PD-9) claim 1 , hydroquinone dihydroxyethyl ether (HQEE) claim 1 , diethylene glycol claim 1 , propylene glycol claim 1 , trimethylolpropane claim 1 , and glycerol.4. The composition of claim 1 , wherein the borate ion source is selected from the group consisting of boric acid claim 1 , borax claim 1 , calcium borate claim 1 , sodium borate claim 1 , sodium tetraborate claim 1 , disodium tetraborate claim 1 , and any combination there of.5. The composition of claim 1 , wherein the epoxy resin is selected from the group consisting of ethylene glycol diglycidyl ether (EGDGE) claim 1 , n-butyl glycidyl ether (BGE) claim 1 , polypropylene glycol diglycidyl ether (PPGDGE) claim 1 , and polyethylene glycol diglycidyl ether (PEGDGE).6. The composition of claim 1 , wherein the compound comprising one or more thiol groups is selected from the group consisting of pentaerythritol tetra(3-mercapto-propionate) (PETMP); trimethylol-propane tri(3-mercapto-propionate) (TMPMP); glycol di(3-mercapto-propionate) (GDMP); tris[25-(3-mercapto-propionyloxy)ethyl]isocyanurate (TEMPIC); dipentaerythritol hexa(3-mercapto-propionate) ...

Antifouling coating composition, antifouling coating film, substrate with antifouling coating film, and production process for the substrate

The present invention relates to an antifouling coating composition, an antifouling coating film, a substrate with an antifouling coating film and a production process for the substrate. The antifouling coating composition includes a hydrolyzable polymer (A) having a structural unit represented by the following formula (1) and having a weight-average molecular weight of 1000 to 5000 and an antifouling agent (B) including (b1) 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile, and has a volatile organic compound (VOC) content of not more than 400 g/L. [In the formula (1), M represents zinc or copper, and R 1 independently represents a hydrogen atom or a methyl group.]

CURABLE COMPOSITION, LITHOGRAPHIC PRINTING PLATE PRECURSOR, AND METHOD FOR PRODUCING LITHOGRAPHIC PRINTING PLATE

A curable composition includes an infrared absorber having at least one element in Group XIII of the periodic table on a mother nucleus structure and having a chain-like polymethine structure, in which two or more hetero atoms are bonded to carbon atoms at non-meso positions. Also, a lithographic printing plate precursor in which the curable composition is used, and a method for producing a lithographic printing plate in which the lithographic printing plate precursor is used are provided. 1. A curable composition comprising:an infrared absorber comprising at least one element in Group XIII of the periodic table on a mother nucleus structure and comprising a chain-like polymethine structure.2. The curable composition according to claim 1 , wherein claim 1 , in the infrared absorber claim 1 , an anion charge is present on the element in Group XIII in a resonant structure formula.3. The curable composition according to claim 1 , wherein the element in Group XIII of the periodic table comprises at least one selected from the group consisting of boron and aluminum.4. The curable composition according to claim 1 , wherein the chain-like polymethine structure comprises a chain-like polymethine structure in which two or more hetero atoms are bonded to carbon atoms at non-meso positions.5. The curable composition according to claim 4 , wherein the infrared absorber comprises two or more boron atoms claim 4 , and each of the two or more hetero atoms comprises at least one selected from the group consisting of an oxygen atom and a nitrogen atom.6. The curable composition according to claim 4 , wherein the infrared absorber comprises two or more boron atoms claim 4 , and the two or more hetero atoms comprises four or more oxygen atoms.10. The curable composition according to claim 1 , further comprising:a polymerizable compound; anda polymerization initiator.11. The curable composition according to claim 10 , wherein the polymerization initiator comprises an onium salt ...

PHOTOCONTROLLED DYNAMIC COVALENT LINKERS FOR POLYMER NETWORKS

Reversibly crosslinkable polymeric networks, including reversibly crosslinkable hydrogel networks are provided. Also provided are methods of making the polymeric networks and methods of using the hydrogel networks in tissue engineering applications. The reversibly crosslinkable polymeric networks are composed of polymer chains that are covalently crosslinked by azobenzene boronic ester bonds that can be reversibly formed and broken by exposing the polymeric networks to different wavelengths of light. 1. A reversibly crosslinkable composition comprising:a first molecule comprising at least two terminal azobenzene boronic acid groups; anda second molecule comprising at least two terminal diol groups, wherein at least one of the first and second molecules is a polymer, and further wherein, if the first molecule has only two terminal azobenzene boronic acid groups, then the second molecule comprises at least three terminal diol groups, and if the second molecule has only two terminal diol groups, the first molecule has at least three terminal azobenzene boronic acid groups;wherein the first molecule is characterized in that its azobenzene groups undergo a reversible E to Z isomerization upon irradiation with ultraviolet light, visible light, or infrared light, and its boronic acid groups react with the terminal diol groups of the second polymer to form a polymer network comprising covalent azobenzene boronic ester bonds.2. The composition of claim 1 , wherein one or both of the first molecule and the second molecule comprise polysaccharide chains.3. The composition of claim 2 , wherein the polysaccharide chains comprise hyaluronic acid chains.4. The composition of claim 1 , wherein one or both of the first molecule and the second molecule comprise poly(ethylene glycol) chains.5. The composition of claim 1 , wherein one or both of the first molecule and the second molecule comprise decellularized extracellular matrix.6. The composition of claim 1 , wherein one or both of ...

STORAGE STABLE EPOXY RESIN COMPOSITION

The present invention relates to the use of boronic acids to increase the storage stability of epoxy resin compositions and epoxy resin compositions comprising an epoxy resin, a curing agent, a curing accelerator and a boronic acid. 2. Use according to claim 1 , wherein radical Rin formula (I) means:{'sup': '1', 'R=methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decanyl, hydroxymethyl, 2-hydroxyethyl, 3 -hydroxypropyl, 4-hydroxybutyl or 5-hydroxypentyl.'}3. Use according to claim 1 , wherein Rin formula (I) is a radical of formula (II) claim 1 , wherein radicals R claim 1 , R claim 1 , Rmean:{'sup': '2', 'sub': 1', '5', '2, 'R=fluorine, chlorine, bromine, iodine, cyano, Cto Calkyl, alkoxy, acyl, alkylsulfonyl, aryl, carboxyl or B(OH),'}{'sup': 3', '4, 'R, R=hydrogen.'}4. Use according to claim 1 , wherein Rin formula (I) is a radical of formula (II) claim 1 , wherein radicals R claim 1 , R claim 1 , Rindependently of one another mean:{'sup': 2', '3, 'sub': 1', '5', '2, 'R, R=independently of one another fluorine, chlorine, bromine, iodine, cyano, Cto Calkyl, alkoxy, acyl, alkylsulfonyl, aryl, carboxyl or B(OH),'}{'sup': '4', 'R=hydrogen.'}5. Use according to claim 1 , wherein Rin formula (I) is a radical of formula (II) claim 1 , wherein radicals R claim 1 , R claim 1 , Rindependently of one another mean:{'sup': 2', '3', '4, 'sub': 1', '5', '2, 'R, R, R=fluorine, chlorine, bromine, iodine, cyano, Cto Calkyl, alkoxy, acyl, alkylsulfonyl, aryl, carboxyl or B(OH).'}9. Epoxy resin composition according to claim claim 1 , wherein the epoxy resin composition based on 100 parts by weight of epoxy resin comprises:a) 1 to 15 parts by weight of curing agent, 'c) 0.05 to 3.0 parts by weight of boronic acid according to formula (I).', 'b) 0.1 to 9 parts by weight of curing accelerator, and'}10. Epoxy resin composition according to claim 7 , wherein the weight ratio of curing agent to boronic acid ...

Composition, method of manufacturing composition, curable composition, cured film, near-infrared cut filter, solid-state imaging device, infrared sensor, and camera module

Provided are a composition of which dispersibility of particles including a pyrrolopyrrole coloring agent is satisfactory, a method of manufacturing a composition, a curable composition, a cured film using a curable composition, a near-infrared cut filter, a solid-state imaging device, an infrared sensor, and a camera module. The composition includes particles including a coloring agent represented by Formula (1), in which an average secondary particle diameter of the particles is 500 nm or less. R 1a and R 1b each independently represent an alkyl group, an aryl group, or a heteroaryl group, R 2 and R 3 each independently represent a hydrogen atom or a substituent, R 2 and R 3 may be bonded to each other to form a ring, R 4 's each independently represent a hydrogen atom, an alkyl group, an aryl group, a heteroaryl group, —BR 4A R 4B , or a metal atom, R 4 's may form a covalent bond or a coordinate bond with at least one selected form R 1a , R 1b , or R 3 , and R 4A and R 4B each independently represent a hydrogen atom or a substituent.

Method of crosslinking glycosaminoglycans

A new hydrogel made of crosslinked glycosaminoglycans, particularly crosslinked hyaluronic acid, chondroitin or chondroitin sulfate, having reversible linkages using boronic acid or boroxole derivatives leading to new benefits. Glycosaminoglycans that are crosslinked via an alkoxyboronate ester anion formed between a diol portion of a diol-functional moiety grafted to a first glycosaminoglycan and a boronate hemiester grafted to a second glycosaminoglycan.

Curable composition, film, optical film, light-emitting display element panel, and light-emitting display

To provide a curable composition which can easily form an optical film with good fluorescence efficiency and includes quantum dots (B), a film made of a cured product of the curable composition, an optical film for a light-emitting display element made of the film, a light-emitting display element panel including the optical film, and a light-emitting display equipped with the light-emitting display element panel. A film is formed by curing a curable composition which includes an epoxy compound (A) having two or more epoxy groups and including a cyclic structure other than an oxirane ring, quantum dots (B), and an acid generator (C).

POLYMERIC LAYER AND ORGANIC ELECTRONIC DEVICE COMPRISING SAME.

Polymeric layers suitable for organic layers of electronic devices that show reduced driving voltage and/or increased luminous efficiency. 7. The polymeric layer of claim 1 , wherein L in Structure D is selected from -alkylene- claim 1 , -arylene- claim 1 , -alkylene-arylene- claim 1 , -arylene-alkylene- claim 1 , or a covalent bond.11. The polymeric layer of claim 1 , wherein Monomer B has a molecular weight of from 500 g/mole to 28 claim 1 ,000 g/mole.12. The polymeric layer of claim 1 , wherein Monomer B has a purity equal to or above 99%.14. An organic electronic device comprising a polymeric layer of .15. The organic device of claim 14 , wherein the electronic device is a light emitting device. The present invention relates to a polymeric layer and an organic electronic device comprising the polymeric layer.Organic electronic devices are endowed with advantages such as flexibility, low power consumption, and relatively low cost over conventional inorganic electronic devices. Organic electronic devices usually include organic light emitting devices such as an organic light emitting diode (OLED). OLEDs have a multi-layer structure and typically include an anode and a metal cathode. Sandwiched between the anode and the metal cathode are organic layers such as a hole injection layer (HIL), a hole transport layer (HTL), an emitting material layer (EML), an electron transport layer (ETL) or an electron injection layer (EIL).Key properties for materials for these organic layers include long lifetime, reduced driving voltage and/or increased luminous efficiency to minimize power consumption in OLED displays, especially for mobile applications where batteries are used as power sources. In the case of HTL layer, the process by which the layer is deposited is also critical for its end-use application.Methods for depositing HTL layer, in small display applications, usually involve evaporation of a small organic compound with a fine metal mask to direct the deposition. In ...

Method for Modifying and Controlling the Threshold Voltage of Thin Film Transistors

Doped semiconductor ink formulations, methods of making doped semiconductor ink formulations, methods of coating or printing thin films, methods of forming electronic devices and/or structures from the thin films, and methods for modifying and controlling the threshold voltage of a thin film transistor using the films are disclosed. A desired dopant may be added to an ink formulation comprising a Group IVA compound and a solvent, and then the ink may be printed on a substrate to form thin films and conductive structures/devices, such as thin film transistors. By adding a customized amount of the dopant to the ink prior to printing, the threshold voltage of a thin film transistor made from the doped semiconductor ink may be independently controlled upon activation of the dopant. 1. A thin film transistor , capacitor , diode , resistor device , circuit , RFID tag , display backplane , sensor and/or photovoltaic device , comprising a semiconductor film having 0.1 to 50 ppm of dopant atoms therein.2. The device of claim 1 , wherein the semiconductor film comprises a printed doped silicon film on a substrate.3. The device of claim 2 , wherein the dopant atoms comprise B claim 2 , P claim 2 , As claim 2 , or Sb.4. The device of claim 1 , wherein the semiconductor film comprises 1-10 ppm of dopant atoms therein.5. The device of claim 4 , wherein the device is a thin film transistor.6. The device of claim 4 , wherein the dopant atoms are present in an amount sufficient to control a threshold voltage of the thin film transistor.7. The device of claim 2 , further comprising a conductor on the printed doped silicon film.8. A method of controlling a threshold voltage of a thin film transistor comprising:a) making a semiconductor ink comprising a Group IVA compound containing at least five Si and/or Ge atoms, a dopant in an amount effective to provide a film with a dopant atom concentration of from 0.1 to 50 ppm, relative to the number of Group IVA atoms, and a solvent;b) ...

ELECTROCHROMIC DEVICE

Disclosed are curved electrochromic devices comprising an electrochromic apparatus disposed between first and second curved layers of transparent material, and the first and second curved layers have exterior and inner surfaces, wherein the inner surfaces face the electrochromic apparatus. Also disclosed are processes for manufacturing the disclosed bubble visors. 1. A curved electrochromic device comprising an electrochromic apparatus disposed between first and second curved layers of transparent material , and the first and second curved layers have exterior and inner surfaces , wherein the inner surfaces face the electrochromic apparatus , and wherein the exterior surface of the first curved layer of transparent material is provided with a coating that blocks wavelengths of visible radiation capable of initiating chemical decomposition of the electrochromic apparatus.2. A curved electrochromic device according to claim 1 , wherein the transparent material of each of the first and second curved layers is independently glass or thermoplastic polymer.3. A curved electrochromic device according to claim 1 , wherein the electrochromic apparatus comprises an electrolyte membrane comprising a non-aqueous electrolyte and a polymer claim 1 , and the electrolyte membrane has a membrane first surface and a membrane second surface.4. A curved electrochromic device according to claim 3 , wherein the non-aqueous electrolyte is an ionic liquid.5. A curved electrochromic device according to claim 4 , wherein the ionic liquid comprises an anion selected from the group consisting of sulfates claim 4 , alkylsulfates claim 4 , arylsulfates claim 4 , alkylsulfonates claim 4 , fluorinated alkylsulfates claim 4 , fluorinated alkylsulfonates claim 4 , fluoroalkylsulfonylimides claim 4 , hexafluorophosphate claim 4 , tetracyanoborate claim 4 , tetrafluoroborate claim 4 , thiocyanate claim 4 , thiosalicylate claim 4 , dicyanamide claim 4 , and halides.6. A curved electrochromic device ...

NITROGEN-CONTAINING CYCLIC COMPOUND AND COLOR CONVERSION FILM COMPRISING SAME

The present specification relates to a compound containing nitrogen, and a color conversion film, a backlight unit, and a display device, including the same. 2. The compound of claim 1 , wherein at least one of R6 claim 1 , R8 claim 1 , R9 claim 1 , and R11 is —C(═O)OR; a monocyclic or polycyclic cycloalkyl group; or a monocyclic or polycyclic aliphatic heterocyclic group claim 1 , R is a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group claim 1 , and the others of R6 to R8 claim 1 , R9 claim 1 , and R11 are hydrogen; deuterium; a nitrile group; or a substituted or unsubstituted alkyl group.3. The compound of claim 1 , wherein at least one of R6 and R8 and at least one of R9 and R11 are —C(═O)OCH; —C(═O)OCHCH; a substituted or unsubstituted cyclohexyl group; a substituted or unsubstituted cyclopentyl group; a substituted or unsubstituted cycloheptyl group; a substituted or unsubstituted cyclooctyl group; a substituted or unsubstituted bicycloheptyl group; a substituted or unsubstituted bicyclooctyl group; a substituted or unsubstituted tetrahydropyran group; or a substituted or unsubstituted adamantane group claim 1 , and the others of R6 claim 1 , R8 claim 1 , R9 claim 1 , and R11 are hydrogen; deuterium; a nitrile group; or a substituted or unsubstituted methyl group.4. The compound of claim 1 , wherein at least one of R6 and R8 and at least one of R9 and R11 are the same as or different from each other claim 1 , and are each independently —C(═O)OCH; —C(═O)OCHCH; a cyclohexyl group which is unsubstituted or substituted with a methyl group or a methoxy group; a cyclopentyl group; a cycloheptyl group; a cyclooctyl group; a bicycloheptyl group which is unsubstituted or substituted with a phenyl group; a tetrahydropyran group; or a substituted or unsubstituted adamantane group claim 1 , and the others of R6 claim 1 , R8 claim 1 , R9 claim 1 , and R11 are hydrogen; deuterium; a nitrile group; or a substituted or unsubstituted methyl ...

NITROGEN-CONTAINING COMPOUND, COLOR CONVERSION FILM INCLUDING SAME, AND BACKLIGHT UNIT AND DISPLAY DEVICE INCLUDING SAME

Provided are a nitrogen-containing ring compound of the following Chemical Formula 1: 2. The compound of claim 1 , wherein R7 is a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms claim 1 , a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms claim 1 , or a substituted or unsubstituted aralkyl group having 6 to 30 carbon atoms.3. The compound of claim 1 , wherein R1 claim 1 , R3 claim 1 , R4 claim 1 , and R6 are identical to or different from one another claim 1 , and are each independently hydrogen claim 1 , a substituted or unsubstituted methyl group claim 1 , a substituted or unsubstituted cyclohexyl group claim 1 , a substituted or unsubstituted cyclopentyl group claim 1 , a substituted or unsubstituted cycloheptyl group claim 1 , a substituted or unsubstituted cyclooctyl group claim 1 , a substituted or unsubstituted bicycloheptyl group claim 1 , a substituted or unsubstituted bicyclooctyl group claim 1 , a substituted or unsubstituted tetrahydropyranyl group claim 1 , a substituted or unsubstituted phenoxy group claim 1 , a substituted or unsubstituted phenyl group claim 1 , or a substituted or unsubstituted naphthyl group.4. The compound of claim 1 , wherein R1 claim 1 , R3 claim 1 , R4 claim 1 , and R6 are a substituted or unsubstituted cyclohexyl group.5. The compound of claim 1 , wherein X1 and X2 are identical to or different from one another claim 1 , and are each independently a halogen group claim 1 , a cyano group claim 1 , a substituted or unsubstituted alkoxy group claim 1 , or a substituted or unsubstituted aryloxy group.7. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a 1 nm to 100 nm lower maximum emission peak than a compound wherein R1 to R7 claim 1 , X1 and X2 are the same as in the compound of Chemical Formula 1 except that R7 is directly bonded to the core structure without the NH linker.8. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a 1 nm to ...

Epoxy resin composition, prepreg, and fiber-reinforced composite material

The present invention provides an epoxy resin composition that serves to produce a cured epoxy resin that simultaneously realizes a high heat resistance, a high elastic modulus, and a low color and to produce a molded article having a good appearance without suffering the formation of white spots on the surface thereof when used as matrix resin in a fiber reinforced composite material. The epoxy resin composition includes an epoxy resin as component [A], an aromatic urea [B1] and/or an imidazole compound [B2] as component [B], and a borate ester compound as component [C], containing dicyandiamide in the amount of 0.5 part by mass or less relative to the total quantity of epoxy resins which accounts for 100 parts by mass, wherein the epoxy resin composition meets certain sets of further requirements with respect to its composition.

POLYUREA-POLY(METH)ACRYLATE INTERPENETRATING POLYMER NETWORK ADHESIVE COMPOSITIONS AND METHODS OF USING THE SAME

Provided herein are adhesive compositions comprising a polyurea-poly(meth)acrylate interpenetrating polymer network. Further provided are two-part curable adhesive compositions comprising a Part A initiator composition and a Part B activator composition. The Part A initiator composition comprises an organoborane-amine complex and the Part B activator composition comprises an isocyanate that is reactive with the amine portion of the organoborane-amine complex to liberate organoborane from the organoborane-amine complex. Further provided are methods of using an adhesive composition comprising a polyurea-poly(meth)acrylate interpenetrating polymer network, such as, for example, in joining and/or bonding together polyolefin materials (e.g., polypropylene random copolymer (PP-R) pipes). 1. An adhesive composition comprising a polyurea-poly(meth)acrylate interpenetrating polymer network formed from a reaction mixture of a two-part curable adhesive composition comprising a Part A initiator composition and a Part B activator composition ,wherein the Part A initiator composition comprises an organoborane-amine complex and at least one amine terminated liquid polymer; and the Part B activator composition comprises at least one polyisocyanate, at least one free radically polymerizable monomer, and at least one compound having at least two free radically polymerizable ethylenically unsaturated groups.2. The adhesive composition of claim 1 , wherein the reaction mixture comprises a volume ratio of the Part A initiator composition to the Part B activator composition in a range of 1:4 to 1:20.3. The adhesive composition of claim 1 , wherein the organoborane-amine complex is a trialkylborane-amine complex.4. The adhesive composition of claim 3 , wherein the trialkylborane-amine complex is tri-n-butylborane methoxypropylamine.5. The adhesive composition of claim 1 , wherein the at least one amine terminated liquid polymer has a hydrophobic flexible backbone.6. The adhesive ...

DICHROIC DYE COMPOUND, POLARIZING FILM, AND USES THEREOF

A compound having a maximum absorption in a wavelength range of 350 nm to 550 nm that functions as a dichroic dye is provided. In particular, a compound represented by formula (1) is provided. In the compound of formula (1), Rrepresents an alkyl group having 1 to 20 carbon atoms or the like; Rrepresents an acyl group having 1 to 20 carbon atoms or the like; Rrepresents a hydrogen atom or the like; and Y represents a group of formula (Y1). In the formula (Y1), * represents a bonding site with N, or a group of formula (Y2). In the formula (Y2), * represents a bonding site with N; Pand Peach independently represent —S— or the like; and Qand Qeach independently represent ═N— or the like. 2. The compound according to claim 1 , wherein p claim 1 , q claim 1 , and r are 0.3. A composition comprising a polymerizable liquid crystal compound and the compound according to .4. The composition according to claim 3 , wherein the polymerizable liquid crystal compound exhibits a smectic liquid crystal phase.5. The composition according to claim 3 , further comprising a polymerization initiator.6. A polarizing film comprising the compound according to .7. A polarizing film formed of the composition according to .8. The polarizing film according to claim 6 , wherein a maximum absorption wavelength (λ) of the polarizing film is longer than a maximum absorption wavelength (λ) of the compound represented by formula (1).9. The polarizing film according to claim 8 , wherein a difference between λand λis not less than 15 nm.10. The polarizing film according to claim 6 , wherein a Bragg peak is exhibited in X-ray diffractometry.11. A liquid crystal display device comprising the polarizing film according to .12. A liquid crystal cell comprising the polarizing film according to claim 6 , a liquid crystal layer claim 6 , and a base.13. The liquid crystal cell according to claim 12 , wherein the polarizing film is disposed between the base and the liquid crystal layer.14. The liquid crystal ...

POLARIZING PLATE PROTECTIVE FILM, POLARIZING PLATE, AND DISPLAY DEVICE

A polarizing plate protective film which prevents deterioration of polarization performance in a high temperature, high humidity environment, and a polarizing plate and display device using the film including a compound represented by the following General Formula (I). 3. The polarizing plate protective film according to claim 1 ,wherein the compound represented by General Formula (I) includes at least one benzene ring.4. The polarizing plate protective film according to claim 1 ,wherein the compound represented by General Formula (I) is represented by General Formula (II-1) or (II-3).5. The polarizing plate protective film according to claim 1 ,wherein the n is an integer of 2 to 4, and the total number of carbon atoms of component parts other than X is equal to or smaller than 40.6. The polarizing plate protective film according to claim 1 ,wherein the number of shortest linking atoms which link two X's with each other is equal to or smaller than 20 between every two X's.7. The polarizing plate protective film according to claim 1 ,{'sub': 2', '2', '2', '2', '2', '2', '2, 'sup': a1', 'a2', 'a3', 'a1', 'a3, 'wherein the Z is a single bond, —O—, —S—, —SO—, —SO—, —OC(═O)—, —C(R)(R)—, >C<, (—OCHCH)C(CHCHO—), >C(R)—, >N—, or —N(Ra)—, Rto Reach independently represent a hydrogen atom, an alkyl group, or an aryl group, and Ra represents a hydrogen atom, an alkyl group, an aryl group, or an acyl group.'}8. The polarizing plate protective film according to claim 1 , including cellulose acylate.9. A polarizing plate comprising:{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'the polarizing plate protective film according to on both sides or one side of a polarizer.'}11. A display device comprising at least one polarizing plate according to . This application is a Continuation of PCT International Application No. PCT/JP2015/080789 filed on Oct. 30, 2015, which claims priority under 35 U.S.C. §119 (a) to Japanese Patent Application No. 2014-223775 filed on Oct. 31, 2014, ...

Viscoelastic silicone rubber compositions

The invention provides for new viscoelastic silicone rubbers and compositions and methods for making and using them. The invention provides for viscoelastic silicone rubbers that are stiffer on short timescales than they are on long timescales. When subjected to brief stresses, they are relatively stiff and elastic, and they resist changing shapes. When subjected to sustain stresses, however, they are relatively soft and accommodating, and they gradually change shapes. When those stresses are removed, they gradually return to their original shapes. These viscoelastic silicone rubbers resist compression set and they are extremely resilient in response to sudden impacts. They can be dense rubbers, foam rubbers, and particles.

COMPOSITION

An object of the present invention is to provide a two-part composition containing a first agent and a second agent: the first agent comprising (1) (meth)acrylate and (2) organoboron compound, and having an oxygen content of 5 ppm or less, and the second agent comprising (3) phosphate ester. 1. A two-part composition containing a first agent and a second agentthe first agent comprising (1) (meth)acrylate and (2) organoboron compound, and having an oxygen content of 5 ppm or less, andthe second agent comprising (3) phosphate ester.3. The composition according to claim 1 , wherein (3) phosphate ester is used in 0.5 to 20 parts by mass with respect to 100 parts by mass of (1) (meth)acrylate.4. The composition according to claim 1 , wherein (1) (meth)acrylate contains (1-1) (meth)acrylate having a cyclic ether skeleton.5. The composition according to claim 1 , wherein (1) (meth)acrylate contains (1-1) (meth)acrylate having a cyclic ether skeleton and (1-2) (meth)acrylate having an aliphatic hydrocarbon group.6. The composition according to claim 1 , wherein (2) organoboron compound is an alkylborane-amine complex.7. The composition according to claim 6 , wherein the alkylborane-amine complex is one or more of the groups consisting of triethylborane-1 claim 6 ,3-diaminopropane complex claim 6 , triethylborane-diethylenetriamine complex claim 6 , and tributylborane-3-methoxy-1-propylamine complex.8. The composition according to claim 1 , wherein (2) organoboron compound is used in 0.01 to 10 parts by mass with respect to 100 parts by mass of (1) (meth)acrylate.9. The composition according to claim 1 , wherein at least one of the first agent and the second agent further contains (4) elastomer component.10. A curable resin composition containing the composition according to .11. An adhesive composition containing the composition according to .12. The adhesive composition according to claim 11 , which being used for adhering an adhered body comprising one or more of the ...

Extruded pet films with photostable dyes for color conversion

A color converter may include (a) a polyethylene terephthalate matrix material; and (b) an organic fluorescent dye selected from a compound of formulae (I.a), (I.b), (I.c) or mixtures thereofwherein EWG1 and EWG2 are CN, CH(O), C(O)R13, OC(O)R13, COOR14, CH(COOR14)2, SO2R14, C(O)NR15R16, SO2NR15R16, or C1-C20-fluoroalkyl; R1, R2, R3, R4, R5, R6, R7a, R7b, R7c, R13, R14, R15 and R16 are as defined in the claims and in the description. A backlight unit, a liquid crystal display module, and a light emitting device may include such a color converter. In compounds of formula (I.b) EWG1 and EWG2 may be CN.

CONDUCTIVE MEMBER, CONDUCTIVE ROLLER AND IMAGE FORMING DEVICE

The conductive member of this disclosure is formed of a UV cure resin obtained by curing under ultraviolet ray radiation a composition containing a urethane (meth)acrylate oligomer (A), a photo polymerization initiator (B) and an ionic conductive agent (C), wherein: the ionic conductive agent (C) contains an organic boron complex salt and a compound having a structure expressed with the following general formula(1), and a compounding amount of the organic boron complex salt is 0.2 parts by mass or more per 100 parts by mass of a curing component in the composition. 1. A conductive member formed of a UV cure resin obtained by curing under ultraviolet ray radiation a composition containing a urethane (meth)acrylate oligomer (A) , a photo polymerization initiator (B) and an ionic conductive agent (C) , wherein:the ionic conductive agent (C) contains an organic boron complex salt and a compound having a structure expressed with the following general formula(1), and {'br': None, 'sub': 2', '2, '—SO—NX—SO— \u2003\u2003(1)'}, 'a compounding amount of the organic boron complex salt is 0.2 parts by mass or more per 100 parts by mass of a curing component in the composition.'}(In the general formula (1), X represents an alkali metal.)2. The conductive member according to claim 1 , wherein: the compounding amount of the compound having the structure represented with the aforementioned general formula (1) is 0.1 to 4.0 parts by mass per 100 parts by mass of the curing component in the composition.3. The conductive member according to claim 1 , wherein: the organic boron complex salt is an organic boron complex potassium salt.4. The conductive member according to claim 1 , wherein: the alkali metal X in the general formula (1) is potassium.5. The conductive member according to claim 1 , wherein: the composition which is cured by radiating ultraviolet ray further contains a monomer having a hydroxyl group skeleton.6. A conductive roller comprising:a shaft member, and{'claim-ref': ...

COLOR CONVERSION FILM, PRODUCTION METHOD FOR SAME, AND BACKLIGHT UNIT AND DISPLAY DEVICE COMPRISING SAME

The invention described in the present specification relates to a color conversion film including a resin matrix; and an organic fluorescent substance dispersed in the resin matrix, wherein the organic fluorescent substance includes a green fluorescent substance having a maximum light emission wavelength in a 510 nm to 560 nm range when irradiating light including a 450 nm wavelength, and a red fluorescent substance having a maximum light emission wavelength in a 600 nm to 660 nm range when irradiating light including a 450 nm wavelength, the green fluorescent substance and the red fluorescent substance have a molar ratio of 5:1 to 50:1, and the color conversion film has a light emission peak with a full width at half maximum (FWHM) of 50 nm or less in a 510 nm to 560 nm range and a light emission peak with a FWHM of 90 nm or less in a 600 nm to 660 nm range when irradiating light, a method for preparing the same, and a backlight unit including the color conversion film. 1. A color conversion film comprising:a resin matrix; andan organic fluorescent substance dispersed in the resin matrix,wherein the organic fluorescent substance includes a green fluorescent substance having a maximum light emission wavelength in a 510 nm to 560 nm range when irradiating light including a 450 nm wavelength, and a red fluorescent substance having a maximum light emission wavelength in a 600 nm to 660 nm range when irradiating light including a 450 nm wavelength, the green fluorescent substance and the red fluorescent substance have a molar ratio of 5:1 to 50:1, and the color conversion film has a light emission peak with a full width at half maximum (FWHM) of 50 nm or less in a 510 nm to 560 nm range and a light emission peak with a FWHM of 90 nm or less in a 600 nm to 660 nm range when irradiating light.2. The color conversion film of claim 1 , which has a light emission peak with a FWHM of 70 nm or less in a 610 nm to 650 nm range.3. The color conversion film of claim 1 , wherein ...

Curable resin composition, production method of image sensor chip using the same, and image sensor chip

There is provided a curable resin composition which is capable of being coated so as to have a film thickness of 20 μm or more and contains a dye having a maximum absorption wavelength in a wavelength range from 600 to 850 nm, and the infrared ray cut filter having a dye-containing layer having a film thickness of 20 μm or more formed from the curable resin composition, and a production method of image sensor chip comprising a step of coating the curable resin composition on a glass substrate to form a dye-containing layer, and a step of adhering the glass plate having the dye-containing layer formed on a solid-state imaging device substrate.

Rubber-metal adhesion promoter, rubber composition, and tire

A rubber-metal adhesion promoter characterized by including: a metal salt (1) of a carboxylic acid which is a metal salt of an aliphatic carboxylic acid having 2 to 25 carbon atoms and in which the metal is bismuth, copper, antimony, silver or niobium; or a compound (2) represented by the following general formula (A): [wherein Z represents a structure selected from the following formulae (z-1) to (z-4); M represents bismuth, copper, antimony, silver or niobium; (RCOO) represents a residue of an aliphatic carboxylic acid having 2 to 25 carbon atoms; and x represents the valence of M minus 1].

CURABLE COMPOSITION, CURED PRODUCT OF THE CURABLE COMPOSITION, AND METHOD OF PRODUCING A CURED PRODUCT USING THE CURABLE COMPOSITION

A cationically polymerizable curable composition comprising a compound having a vinyloxy group bonded to an aromatic group which is easily cured upon light exposure and/or heating, a cured product of the curable composition, and a method of producing a cured product using the curable composition. In a cationically polymerizable curable composition that includes a compound having a vinyloxy group bonded to an aromatic group, a sulfonium salt having a specific structure is used as a curing agent. A cured product is produced by shaping the curable composition into a predetermined shape, and subjecting the shaped curable composition to light exposure and/or heating. 3. The curable composition according to claim 2 , wherein each of Wand Wis a group represented by the formula (2) and the ring Z is a naphthalene ring.4. The curable composition according to claim 1 , wherein the aromatic vinyl ether compound (B) is a compound comprising a fluorene ring.5. The curable composition according to claim 1 , wherein each of Rand Rin the formula (a1) is a phenyl group.6. The curable composition according to claim 1 , wherein Ain the formula (a1) is S.7. The curable composition according to claim 1 , wherein X— in the formula (a1) is an anion selected from the group consisting of SbF claim 1 , PF claim 1 , (CFCF)PF claim 1 , (CF)B claim 1 , ((CF)CH)B claim 1 , (CF)Ga claim 1 , ((CF)CH)Ga claim 1 , and (CFSO)C.8. The curable composition according to claim 1 , wherein the cationic polymerization initiator (A) is comprised in a content of 0.01 parts by mass or more and 30 parts by mass or less in relation to 100 parts by mass of the aromatic vinyl ether compound (B).9. A cured product formed by curing the curable composition according to .10. A method of producing a cured product claim 1 , the method comprising:{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'shaping the curable composition according to into a predetermined shape; and'}subjecting the shaped curable composition to at ...

LOW SURFACE ENERGY ACCELERATED BONDING ADHESIVE FORMULATION AND PROCESS FOR THE USE THEREOF

An adhesive two-part formulation is provided that includes an amount of free-radical curable monomers, each of said free-radical curable monomers containing at least one acrylate moiety or at least one methacrylate moiety, a Lewis acid, a thermoplastic resin; and a polymeric impact modifier. Also present in the formulation is an amount of an activator of borane-amine complex, a metal accelerator; and a grafted elastomer with a thermoplastic additive. A process of applying the formulation to a substrate includes mixing together the formulation components such that each part has a storage stability at 50° C. for 30 days where the viscosity at 30 days is within 40% of an initial viscosity. The mixture is applied to the substrate and then allowed to cure to achieve an initial strength of at least 1 MPa lap shear strength within 45 minutes.

MULTIFUNCTIONAL PRIMARY AMINE, PROCESS FOR ITS PREPARATION, AND USE THEREOF

The invention relates to a hydrophilically modified multifunctional amine AC which has more than one primary ammo group per molecule, and at least one group per molecule derived from the reaction of an epoxide group with a reactive group selected from the group consisting of secondary amino groups >NH, hydroxyl groups —OH, mercaptan groups —SH, amide groups —CO—NHR, where R can be hydrogen or an alkyl group having from one to twelve carbon atoms, hydroxyester groups, and acid particularly carboxyl groups —COOH, sulphonic acid groups —SOH, and phosphonic acid groups —POH, and preferably, also moieties which are compatible with an epoxy resin, as well as a process for its preparation, and a method of use thereof. 1. A hydrophilically modified multifunctional amine AC which has more than one primary amino group per molecule , and at least one group per molecule derived from the reaction of an epoxide group with a reactive group selected from the group consisting of secondary amino groups >NH , hydroxyl groups —OH , mercaptan groups —SH , amide groups —CO—NHR , where R can be hydrogen or an alkyl group having from one to twelve carbon atoms , hydroxyester groups , and acid groups , particularly carboxyl groups —COOH , sulphonic acid groups —SOH , and phosphonic acid groups —POH , and preferably , also moieties which are compatible with an epoxy resin.2. The hydrophilically modified multifunctional amine AC of which has at least two primary amino groups per molecule.3. The hydrophilically modified multifunctional amine AC of wherein the hydrophilic modification is provided by moieties derived from oxyethylene or oxypropylene moieties or their mixtures.4. A process to make a hydrophilically modified multifunctional amine AC as claimed in claim 1 , by{'sub': 3', '3', '2, 'formation, in the first step, of an amino functional compound AB having blocked primary amino groups through reaction of an amine A having at least one primary amino group per molecule, and a further ...

METAL COMPLEX AND COLOR CONVERSION FILM COMPRISING SAME

The present disclosure relates to a novel compound, a color conversion film, a backlight unit and a display device comprising the same. 4. The compound of claim 1 , wherein Yto Yare the same as or different from each other claim 1 , and each independently CH claim 1 , CF or N.5. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 520 nm to 550 nm in a film state.6. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 520 nm to 550 nm in a film state claim 1 , and a half-width of the light emission peak is 50 nm or less.7. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 610 nm to 650 nm in a film state.8. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 610 nm to 650 nm in a film state claim 1 , and a half-width of the light emission peak is 60 nm or less.9. The compound of claim 1 , wherein the compound of Chemical Formula 1 has quantum efficiency of 0.9 or more.11. A color conversion film comprising:a resin matrix; and{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'the compound of Chemical Formula 1 of dispersed into the resin matrix.'}12. A backlight unit comprising the color conversion film of .13. A display device comprising the backlight unit of . The present application claims priority to and the benefits of Korean Patent Application No. 10-2014-0192221, filed with the Korean Intellectual Property Office on Dec. 29, 2014, the entire contents of which are incorporated herein by reference.The present application relates to a novel metal complex and a color conversion film comprising the same. In addition, the present application relates to a backlight unit and a display device including the color conversion film.Existing light emitting diodes (LED) are obtained either by mixing a green phosphorescent substance ...

Curable composition and optical element obtained using same

Provided is a curable composition which has excellent thin-film curability and which can form, via the application of light and/or heat, a cured product having heat resistance and thermal yellowing resistance at excellent levels. This curable composition contains cationically curable compounds and a cationic-polymerization initiator. The cationically curable compounds include an epoxy compound (A) in an amount of 10 to 90 weight percent of the total weight of the cationically curable compounds, and an oxetane compound (B) in an amount of 5 to 40 weight percent of the total weight of the cationically curable compounds. The cationic-polymerization initiator includes an onium borate salt (C). The onium borate salt (C) preferably has an anionic moiety selected from [(C 6 H 5 )B(C 6 F 5 ) 3 ] − , [(C 6 H 5 )B((CF 3 CF 2 ) 2 C 6 H 2 F) 3 ] − , and [(C 6 H 5 C 6 H 4 )B(C 6 F 5 ) 3 ] − and a cationic moiety selected from arylsulfonium ions.

Compound and color conversion film comprising same, backlight unit, and display device

The present specification relates to a compound, and a color conversion film, a backlight unit and a display apparatus including the same.

AROMATIC POLYCARBONATE RESIN MOLDING

Provided is an aromatic polycarbonate resin molded body, which is obtained by molding a resin molding material containing an aromatic polycarbonate resin (A), in which: the molded body has a thin-walled portion having a thickness of 0.5 mm or less; the molded body has an o-hydroxyacetophenone content of 1 ppm by mass or less and a nitrogen atom content of 15 ppm or less; and the molded body is free of an absorption maximum in a wavelength range of from 500 nm to 600 nm. 1. An aromatic polycarbonate resin molded body , which is obtained by molding a resin molding material comprising an aromatic polycarbonate resin (A) , wherein:the molded body has a thin-walled portion having a thickness of 0.5 mm or less;the molded body has an o-hydroxyacetophenone content of 1 ppm by mass or less and a nitrogen atom content of 15 ppm or less; andthe molded body is free of an absorption maximum in a wavelength range of from 500 nm to 600 nm.2. The aromatic polycarbonate resin molded body according to claim 1 , wherein a length in a longitudinal direction of the molded body is 60 mm or more claim 1 , and a thickness of a region accounting for at least 80% of the molded body is 0.7 mm or less.3. The aromatic polycarbonate resin molded body according to claim 1 , wherein when a total signal intensity observed in a chemical shift region of from 1.5 ppm or more to 1.9 ppm or less at a time of measurement of a proton NMR spectrum is defined as 100 claim 1 , the molded body has a ratio of a total signal intensity observed in a chemical shift region of from 6.3 ppm or more to 6.7 ppm or less of 0.15 or less.4. The aromatic polycarbonate resin molded body according to claim 1 , wherein the resin molding material further comprises a polyether compound (b1) having a polyoxyalkylene structure.5. The aromatic polycarbonate resin molded body according to claim 1 , wherein the resin molding material further comprises an acid-generating compound (b2).6. The aromatic polycarbonate resin molded body ...

Color conversion film, method for producing same, back-light unit and display apparatus

The invention described in the present specification relates to a color conversion film including a resin matrix; and an organic fluorescent substance dispersed in the resin matrix, and absorbing blue or green light and emitting light having a wavelength different from the absorbing light, wherein the resin matrix includes a thermoplastic resin, and the color conversion film has a light emission peak with a FWHM of 60 nm or less, quantum efficiency of 80% or greater and an absorption coefficient of 30,000 M −1 cm −1 or greater at a maximum absorption wavelength when irradiating light having a light emission peak at 450 nm, a FWHM of 40 nm or less and monomodal light emission intensity distribution, a method for preparing the same, and a backlight unit including the color conversion film.

BORONIC POLYMER CROSSLINKING

The object of the invention is polymer compositions comprising cross-linked polymer comprising boronic ester functions enabling exchange reactions, as well as free monofunctional boronic esters. The compositions are obtained from the modification of a polymer by a functionalised boronic ester additive. This polymer can be pre-functionalised boronic ester or functionalised on addition of the said additive. In particular, the invention relates to a process enabling the behaviour of a polymer to be modified by addition of a functional additive, enabling a cross-linked network containing exchangeable boronic ester links to be formed. 2. Combinations to cross-link linear or branched polymers according to claim 1 , wherein G claim 1 , G claim 1 , Gand Gare identical.3. Combinations to cross-link linear or branched polymers according to claim 1 , wherein G claim 1 , G claim 1 , Gand Geach represent claim 1 , independently from one another claim 1 , a functional group chosen among a thiol function claim 1 , a maleimide function claim 1 , a methacrylic function claim 1 , an acrylic function claim 1 , a styrenic function claim 1 , a maleic ester function claim 1 , an isocyanate function claim 1 , an electrophilic olefin claim 1 , a nucleophilic function claim 1 , an alcohol function and an amine function.4. Combinations to cross-link linear or branched polymers according to claim 3 , wherein G claim 3 , G claim 3 , Gand Gare chosen among acrylate claim 3 , acrylamide claim 3 , maleimide claim 3 , methacrylate and vinylic sulfones.5. Combinations to cross-link linear or branched polymers according to claim 3 , wherein the nucleophilic function is chosen among alcohol claim 3 , thiol claim 3 , amine and carboxlic acid.6. Combinations to cross-link linear or branched polymers according to claim 1 , wherein Rx claim 1 , R′x and R″x each represent claim 1 , independently of one another claim 1 , an aliphatic claim 1 , aromatic claim 1 , arylaliphatic or cycloaliphatic radical ...

Coating Method for Surfaces in Chemical Installations

The invention pertains to a method for providing a metallicor concrete surface of a chemical installation with a coating, which comprises the steps of:—providing a two-pack coating composition wherein the first pack comprises an epoxy resin and the second pack comprises an amine curing agent for the epoxy resin, the coating composition further comprising an organoboron compound of the formula (I), wherein X is anorganic group having 1 to 24 carbon atoms and is linked to the boron atom via a carbon-boron bond, and wherein Y is an at least divalent organic group having 2 to 16 carbon atoms, combining the first pack and the second pack to form a coating composition,—applying the coating composition to the surface of a chemical installation to form a coating layer, and—allowing the coating layer to cure at a temperature in the range of −10 to 50° C. A chemical installation provided with a lining of a cured coating composition as specified above, and a suitable coating composition, are also claimed. It has been found that the coating composition as specified herein has a wide application spectrum, and a high chemical resistance. 2. The method according to claim 1 , wherein the coating layer is further subjected to a post-curing step at a temperature above 50° C.3. The method according to claim 1 , wherein the chemical installation is a chimney claim 1 , pipe claim 1 , or tank claim 1 , a cargo tank or a storage tank.4. The method according to claim 1 , wherein the organoboron compound is present in such an amount thatwhen the equivalent ratio of active hydrogens in the curing agent(s) to the epoxy groups present in the composition is 1.00:1.00 or higher, the amount of organoboron compound present in the composition is equal to 1-50% of the molar amount of epoxy groups present in the composition, andwhen the equivalent ratio of active hydrogens in the curing agent(s) to the epoxy groups present in the composition is below 1.00:1.00, the amount of organoboron compound ...

RESIN COMPOSITION

The present invention provides a resin composition that is thermally curable at a temperature of approximately 80° C., excellent in PCT tolerance, and, therefore, suitable as a one-component adhesive to be used during manufacture of image sensor modules or electronic components. The resin composition contains (A) an epoxy resin; (B) a compound represented by formula (1) below; (C) a curing accelerator; and (D) a silane coupling agent. The compound of the (B) component has a content of 1:0.3 to 1:2.5, in terms of an equivalent ratio between epoxy groups in the epoxy resin of the (A) component and thiol groups in the compound of the (B) component, the silane coupling agent of the (D) component has a content of 0.2 parts by mass to 60 parts by mass with respect to 100 parts by mass in total of the (A) component, the (B) component, the (C) component, and the (D) component, and an equivalent ratio between thiol groups in the compound of the (B) component and Si in the silane coupling agent of the (D) is 1:0.002 to 1:1. 2. The resin composition according to claim 1 , further comprising (E) a stabilizer.3. The resin composition according to claim 2 , wherein the stabilizer of the (E) component is at least one selected from the group consisting of liquid boric acid ester compounds claim 2 , aluminum chelate claim 2 , and barbituric acids.4. The resin composition according to claim 1 , wherein the silane coupling agent of the (D) component is at least one selected from the group consisting of 3-glycidoxypropyltrimethoxysilane claim 1 , 2-(3 claim 1 ,4-epoxycyclohexyl)ethyltrimethoxysilane claim 1 , 3-methacryloxypropyltrimethoxysilane claim 1 , and 8-glycidoxyoctyltrimethoxysilane.5. The resin composition according to claim 1 , wherein the curing accelerator of the (C) component is an imidazole-based curing accelerator claim 1 , a tertiary amine-based curing accelerator claim 1 , or a phosphorus compound-based curing accelerator.6. A one-component adhesive containing the ...

Viscoelastic Silicone Rubber Compositions

This invention relates to viscoelastic silicone rubber compositions that are the products of the reaction of: (a) a silanol-terminated polyorganosiloxane base; (b) a boron-containing crosslinking agent; and (c) a siloxane bond-forming crosslinking agent. In a viscoelastic silicone rubber composition of the invention some of the crosslinks, the siloxane crosslinks, are permanent and others of the crosslinks, the boron-containing crosslinks, are temporary. Because a fraction of its crosslinks can come apart and then reform, a viscoelastic silicone rubber composition of the invention can relax stress in response to strain and thus adapt to new shapes. The composition has sufficient permanent crosslinks, however, to establish a permanent equilibrium shape to which the composition will eventually return when not subject to any imposed stress. A viscoelastic silicone rubber composition has sufficient temporary crosslinks to give the composition a stiffness that is greater on short timescales than it is on longer timescales.

COMPOSITE PARTICLES, KIT, MATERIAL, AND METHOD FOR PRODUCING COMPOSITE PARTICLES

The present invention improves the long-term storage stability of an organoborane-Lewis base complex. First composite particles of the present invention include particles of an organic polymer (B), and an organoborane-Lewis base complex (A) contained in the particles. Second composite particles of the present invention include particles of an inorganic compound (B′), and an organoborane-Lewis base complex (A) adsorbed on the particles. 1. Composite particles comprising:particles of an organic polymer (B); andan organoborane-Lewis base complex (A) contained in the particles.2. Composite particles comprising:particles of an inorganic compound (B′); andan organoborane-Lewis base complex (A) adsorbed on the particles.3. The composite particles according to claim 1 , [{'sub': '3', 'a compound represented by BR, wherein each R is independently an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, a saturated or unsaturated alicyclic group having 3 to 20 carbon atoms, or an alkoxy group having 1 to 20 carbon atoms, and two or more of the groups R may be bonded to each other to form a ring; and'}, {'sub': '3', 'a partial oxide of the compound represented by BR.'}], 'wherein an organoborane of the component (A) is at least one selected from4. The composite particles according to claim 1 ,wherein a Lewis base of the component (A) is at least one selected from an amine, an amidine, a hydroxide, and an alkoxide.5. The composite particles according to claim 1 ,{'sup': 1', '2', '1', '2, 'sub': m', '2−m', 'n', '3−n, 'wherein the component (A) is a compound represented by (N(R)(H)RO)BR, wherein Ris an alkyl group having 1 to 20 carbon atoms, Ris an alkylene group having 1 to 20 carbon atoms, R is an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, a saturated or unsaturated alicyclic group having 3 to 20 carbon atoms, or an alkoxy group having 1 to 20 carbon atoms, two of the groups R may be bonded to each other to ...

Polycarbonate resin molding material

Provided is a polycarbonate resin molding material, including an aromatic polycarbonate resin (A), in which the polycarbonate resin molding material has: a content of o-hydroxyacetophenone measured by a predetermined method (1) of 1 ppm by mass or less; and a YI value measured by a predetermined method (2) of 1.21 or less.

POLYCARBONATE RESIN MOLDING MATERIAL

Provided is a polycarbonate resin molding material, including an aromatic polycarbonate resin (A), in which the polycarbonate resin molding material has: a content of o-hydroxyacetophenone measured by a predetermined method (1) of 1 ppm by mass or less; and a YI value measured by a predetermined method (2) of 1.21 or less. 1. A polycarbonate resin molding material , comprising an aromatic polycarbonate resin (A) and a polyether compound (b1) having a polyoxyalkylene structure ,wherein a content of the polyether compound (b1) is from 0.01 part by mass to 5 parts by mass with respect to 100 parts by mass of the aromatic polycarbonate resin (A), andwherein the polycarbonate resin molding material has:a content of o-hydroxyacetophenone measured by the following Method (1) of 1 ppm by mass or less; anda YI value measured by the following Method (2) of 1.21 or less:Method (1): a molded body measuring 50 mm by 80 mm by 0.3 mm thick is produced through use of the polycarbonate resin molding material by an injection molding method at a cylinder temperature of 360° C. and a die temperature of 80° C. for a cycle time of 20 seconds, the molded body is pulverized and dissolved in chloroform, and o-hydroxyacetophenone in the solution is determined by high-performance liquid chromatography;Method (2): a molded body measuring 50 mm by 90 mm by 5 mm thick is produced through use of the polycarbonate resin molding material by an injection molding method at a cylinder preset temperature of 360° C. and a die temperature of 80° C. for a cycle time of 50 seconds, and the YI value of the molded body is measured with a spectrophotometer under conditions of a C light source and a two-degree field of view.213-. (canceled)14. The polycarbonate resin molding material according to claim 1 , wherein the polycarbonate resin molding material has an L value measured by the following Method (3) of 95.94 or more:Method (3): a molded body measuring 50 mm by 90 mm by 5 mm thick is produced through use ...

INCORPORATION OF BORON COMPLEX INTO RESIN

Complexes, compositions, articles of manufacture, and method for making the same are provided herein. In one embodiment, a borate-polyol complex may be prepared by reacting a boron-containing compound and a polyol to form a reaction mixture and then neutralizing the reaction mixture to form a neutralized borate-polyol complex. The neutralized borate-polyol complex may then be used in combination with polymeric resins to form adhesive products, among other material products, which products can be in manufacturing articles. 1. An adhesive composition , comprising:a neutralized borate-polyol complex;a phenol-formaldehyde or resorcinol-formaldehyde resin; andwater.2. The adhesive composition of claim 1 , further comprising one or more material selected from the group consisting of an inorganic filler material claim 1 , an extender claim 1 , an organic filler material claim 1 , an alkali hydroxide material and combinations thereof.3. The adhesive composition of claim 1 , wherein the neutralized borate-polyol complex comprises a borate-polyol complex neutralized with a hydroxide.4. The adhesive composition of claim 3 , wherein the polyol is selected from the group consisting of glycerol claim 3 , ethylene glycol claim 3 , propylene glycol claim 3 , and combinations thereof.5. The adhesive composition of claim 1 , wherein the borate is a boron material derived from the group consisting boric acid claim 1 , sodium borate claim 1 , sodium metaborate and combinations thereof.6. The adhesive composition of claim 1 , wherein the neutralized borate-polyol complex is formed by a process comprising:reacting glycerol and boric acid to form a complex, andadding sodium hydroxide to the complex to neutralize the complex to form the neutralized borate-polyol complex.7. The adhesive composition of claim 1 , wherein the neutralized borate-polyol complex has a pH from greater than 7 to about 11.5.8. The adhesive composition of claim 1 , wherein the adhesive composition comprises:from ...

COMPOSITION, FILM, NEAR INFRARED CUT FILTER, LAMINATE, PATTERN FORMING METHOD, SOLID IMAGE PICKUP ELEMENT, IMAGE DISPLAY DEVICE, INFRARED SENSOR, AND COLOR FILTER

The composition includes two or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C., in which the two or more near infrared absorbing compounds include a first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, and a second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, and a difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm. 1. A composition comprising:two or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C.,wherein the two or more near infrared absorbing compounds includea first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, anda second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, anda difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm.2. The composition according to claim 1 ,wherein in each of the first near infrared absorbing compound and the second near infrared absorbing compound, a ratio A1/A2 of an absorbance A1 at a wavelength of 500 nm to an absorbance A2 at the absorption maximum is 0.04 or lower.3. The composition according to claim 1 ,wherein at least one of the first near infrared absorbing compound or the second near infrared absorbing compound includes at least one ...

COLOR CONVERSION COMPOSITION, COLOR CONVERSION SHEET AND LIGHT SOURCE UNIT INCLUDING THE SAME, DISPLAY, LIGHTING APPARATUS, BACKLIGHT UNIT, LED CHIP, AND LED PACKAGE

A color conversion composition includes the following Component (A) and Component (B): 2. (canceled)3. (canceled)4. The color conversion composition according to claim 1 , wherein when a weight ratio of the partial structure represented by the General Formula (1) to a total amount of the polyester resin contained as the Component (B) is represented as m% by weight claim 1 , msatisfies 10≤m≤60.6. The color conversion composition according to claim 5 , whereinthe polyester resin has at least the partial structure represented by the General Formula (3) in the molecular structure of the polyester resin, and{'sub': 2', '2', '2, 'when a weight ratio of the partial structure represented by the General Formula (3) to a total amount of the polyester resin contained as the Component (B) is represented as m% by weight, msatisfies 20≤m≤70.'}7. The color conversion composition according to claim 5 , wherein when a weight ratio of the partial structure represented by the General Formula (3) to a total amount of the polyester resin contained as the Component (B) is represented as m% by weight claim 5 , and a weight ratio of the partial structure represented by the General Formula (4) to a total amount of the polyester resin contained as the Component (B) is represented as m% by weight claim 5 , mand msatisfy 20≤m+m≤70.9. (canceled)10. (canceled)12. (canceled)15. The color conversion composition according to claim 13 , wherein R claim 13 , R claim 13 , R claim 13 , and Rin the General Formula (8) are the same as or different from each other claim 13 , and{'sup': 3', '5', '6', '8, 'R, R, R, and Rin the General Formula (8) are substituted or unsubstituted phenyl groups or are substituted or unsubstituted alkyl groups.'}16. (canceled)17. The color conversion composition according to claim 1 , wherein the Component (A) contains a light-emitting material that exhibits light emission with a peak wavelength observed in a region of 500 nm or more and 580 nm or less by using excitation ...

COMPOSITION, FILM, COLOR FILTER, SOLID-STATE IMAGING ELEMENT, IMAGE DISPLAY DEVICE, AND METHOD FOR PRODUCING COMPOUND

A composition includes a compound represented by Formula (1) and a pigment. In Formula (1), Rrepresents an (m+n)-valent linking group, Prepresents a polymer chain which has a polyester repeating unit in a main chain, and of which a weight-average molecular weight is 1000 or more, Prepresents a polymer chain which is different from Pand has a repeating unit derived from a monomer having an ethylenically unsaturated bonding group in a main chain, m represents a number of 1 to 9, n represents a number of 1 to 9, and m+n satisfies 4 to 18. 2. The composition according to claim 1 ,{'sup': '1', 'wherein Ris a linking group derived from a polyfunctional thiol.'}4. The composition according to claim 1 ,{'sup': '1', 'wherein the weight-average molecular weight of the polymer chain represented by Pis 1000 to 10000.'}6. The composition according to claim 1 ,{'sup': '1', 'wherein the polymer chain represented by Pincludes a polyester repeating unit in the main chain.'}7. The composition according to claim 6 ,wherein the polyester repeating unit includes a repeating unit derived from a lactone compound.10. The composition according to claim 1 ,{'sup': '2', 'wherein a molecular weight of the repeating unit derived from a monomer having an ethylenically unsaturated bonding group in the polymer chain represented by Pis 1000 or less.'}11. The composition according to claim 1 ,{'sup': '2', 'wherein the polymer chain represented by Pincludes an acid group.'}12. The composition according to claim 1 ,{'sup': '2', 'wherein the polymer chain represented by Pincludes an ethylenically unsaturated bonding group.'}14. The composition according to claim 1 ,wherein a weight-average molecular weight of the compound represented by Formula (1) is 4000 to 30000.15. The composition according to claim 1 ,wherein a dispersity of the compound represented by Formula (1) is 1.0 to 3.0.16. The composition according to claim 1 ,wherein an acid value of the compound represented by Formula (1) is 25 to 200 ...

Wavelength conversion luminescent resin composition, method for producing wavelength conversion luminescent resin composition, wavelength conversion member, and light-emitting element

An object of the present invention is to provide a wavelength conversion luminescent resin composition that exhibits a high quantum yield, a wavelength conversion member, and a light-emitting element; as well as a method for producing the wavelength conversion luminescent resin composition that exhibits a high quantum yield. The present invention provides a wavelength conversion luminescent resin composition that contains at least one compound represented by Formula (1) and a resin. The substituents in the formula are as defined in the present specification.

RUBBER COMPOSITION AND PNEUMATIC TIRE USING SAME

A rubber composition includes a sulfur-crosslinkable diene rubber, from 1 to 100 parts by mass of carbon black and/or from 5 to 150 parts by mass of an inorganic filler, from 0.5 to 30 parts by mass of a sulfur-containing compounding agent, and from 0.01 to 20 parts by mass of a phosphine borane compound based on 100 parts by mass of the sulfur-crosslinkable diene rubber. The rubber composition may be applied in at least one type selected from the group consisting of a capped tread, a side wall, a belt, an inner liner, a carcass, and a bead of a pneumatic tire. 1. A rubber composition comprising:a sulfur-crosslinkable diene rubber;from 1 to 100 parts by mass of carbon black and/or from 5 to 150 parts by mass of an inorganic filler;from 0.5 to 30 parts by mass of a sulfur-containing compounding agent; andfrom 0.01 to 20 parts by mass of a phosphine borane compound based on 100 parts by mass of the sulfur-crosslinkable diene rubber.2. The rubber composition according to claim 1 , wherein said sulfur-containing compounding agent is at least one selected from the group consisting of sulfur claim 1 , sulfur-containing silane coupling agents claim 1 , and sulfur-containing vulcanization accelerators.3. The rubber composition according to claim 1 , wherein:said inorganic filler is silica;said sulfur-containing compounding agent comprises a sulfur-containing silane coupling agent; andthe amount of the sulfur-containing silane coupling agent is from 1 to 20 parts by mass per 100 parts by mass of the sulfur-crosslinkable diene rubber.4. The rubber composition according to claim 2 , wherein:said inorganic filler is silica;said sulfur-containing compounding agent comprises a sulfur-containing silane coupling agent; andthe amount of the sulfur-containing silane coupling agent is from 1 to 20 parts by mass per 100 parts by mass of the sulfur-crosslinkable diene rubber.5. The rubber composition according to claim 1 , wherein the phosphine borane compound is at least one selected ...