ЭПОКСИСИЛОКСАНОВЫЕ КОМПОЗИЦИИ ДЛЯ ПОКРЫТИЙ

Изобретение относится к композициям на основе эпоксиполисилоксана и может применяться для покрытий. Эпоксиполисилоксановую полимерную композицию получают при взаимодействии (мас.%): 20-80 полисилоксана, 20-80 неароматической эпоксидной смолы и 5-40 отверждающей системы. Отверждающая система включает смесь соединений, выбранных из диалкоксифункционального аминосилана, триалкоксифункционального аминосилана и аминофункциональной полисилоксановой смолы, где смесь имеет среднее число функциональных алкоксигрупп 2,0-2,8. Изобретение позволяет получать композиции на основе эпоксиполисилоксана для покрытий и настила пола, показывающие после отверждения улучшенную эластичность и превосходную устойчивость к атмосферным воздействиям и коррозионную стойкость. 4 н. и 17 з.п. ф-л., 3 табл., 5 пр.

ПРИМЕНЕНИЕ АССОЦИАЦИИ СИЛИКОНОВЫХ СОЕДИНЕНИЙ В КАЧЕСТВЕ АГЕНТА СОЧЕТАНИЯ В КРЕМНЕЗЕМСОДЕРЖАЩИХ ЭЛАСТОМЕРНЫХ КОМПОЗИЦИЯХ

Описывается смесь, состоящая из особой ассоциации силиконовых соединений, включающей по меньшей мере один функционализированный полиорганосилоксан (РОS), содержащий на молекулу по меньшей мере одно функциональное силоксиловое звено (МO1), способное химически и/или физически связываться с гидроксильными участками поверхности кремнеземных частиц, и по меньшей мере один функционализированный органосилан (OS), содержащий на молекулу по меньшей мере одно функциональное звено (G1), способное химически и/или физически связываться со звеньями МO1 и/или с гидроксилсодержащими участками кремнеземных частиц, и по меньшей мере одну другую функциональную группу (G2), способную химически и/или физически связываться с эластомерными цепочками, в качестве агента сшивки кремнезем-эластомер в природных или синтетических эластомерных композициях. Техническим результатом является использование смеси в качестве усиливающего наполнителя, включающего кремниевое вещество. 7 с. и 16 з.п. ф-лы, 15 табл.

ЦИКЛОАЛИФАТИЧЕСКАЯ СМОЛА, СПОСОБ ЕЕ ПОЛУЧЕНИЯ И ЕЕ ПРИМЕНЕНИЕ В ВЫСОКОУСТОЙЧИВОМ ПОКРЫТИИ

Изобретение относится к циклоалифатической смоле, содержащей силаны с эпокси- и алкокси-силанольными функциональными группами, полученной реакцией: a) эпокси-функционального силана, имеющего формулугде каждый Rнезависимо выбран из метила, метокси-, этокси- или пропокси-группы; "X" может представлять собой эпокси-циклогексил или глицидокси-группу; и "n" представляет собой целое число от 1 до 6; и b) гидрированного бисфенола, имеющего формулугде Rпредставляет собой метил, этил или атом водорода. Из циклоалифатической смолы можно получать коррозионностойкие покрытия, применяя указанную циклоалифатическую смолу в отдельности или в качестве гибрида с эпоксидными циклоалифатическими смолами или гидрокси-функционализированными полимерами; в обоих случаях при смешении с аминовыми или амино-силоксановыми отвердителями. Полученные покрытия имеют улучшенные физические характеристики атмосфероустойчивости, устойчивости блеска, твердости и ударопрочности. 3 н. и 21 з.п. ф-лы, 4 пр.

НОВЫЕ АРМИРУЮЩИЕ МАТЕРИАЛЫ, ЭЛАСТОМЕРНЫЕ КОМПОЗИЦИИ И ШИНЫ ДЛЯ КОЛЕС ТРАНСПОРТНЫХ СРЕДСТВ, ИХ СОДЕРЖАЩИЕ

Настоящее изобретение относится к способу получения дериватизированного диоксида кремния (SIL-A-B), дериватизированному диоксиду кремния (SIL-A-B), эластомерной композиции, вулканизируемой эластомерной композиции шины для колес транспортного средства, элементу шины для колес транспортного средства и шине для колес транспортного средства. Данный способ включает взаимодействие силанизированного диоксида кремния (SIL-A), соединения формулы (В1) (RSiO1,5)nи радикального инициатора (D). Силанизированный диоксид кремния (SIL-A) получают взаимодействием диоксида кремния (С), силанизирующей добавки формулы (А): (R1)3Si-X и необязательно кислотного катализатора в органическом растворителе. Эластомерная композиция содержит 100 ч./100 ч. каучука по меньшей мере одного твердого диенового эластомерного полимера (Е) и 3 ч./100 ч. каучука дериватизированного диоксида кремния (SIL-A-B). Эластомерная композиция содержит 100 ч./100 ч. каучука твердого диенового эластомерного полимера (Е), 5 ч./100 ч. каучука ...

АДГЕЗИВНАЯ КОМПОЗИЦИЯ

Изобретение относится к устройству для стомы, содержащее отверждаемую под воздействием влаги адгезивную композицию. Композиция содержит реакционно-способный компонент, который содержит реакционно-способный силиконовый полимер или смесь реакционно-способных силиконовых полимеров, компонент на основе клейкого материала, который содержит клеящийся при надавливании силиконовый клейкий материал или смесь клеящихся при надавливании силиконовых клейких материалов, представляющий собой поликонденсированную полиорганосилоксановую смолу, которая является продуктом или продуктами реакции полиорганосилоксана с концевыми силанольными группами и силикатной полиорганосилоксановой смолы, содержащей по меньшей мере одно силокси-звено SiO, или силсесквиоксан, имеющий формулу [RSiO], где каждый R отдельно представляет собой H, алкильную группу, арильную группу, реакционно-способную функциональную группу или алкоксигруппу, и n составляет от 4 до 18, в присутствии основания с получением поликонденсированной ...

Термостойкий полимерный композиционный материал на основе силоксанового каучука и способ его получения

Изобретение относится к теплостойким композиционным материалам, которые могут применяться в различных отраслях техники, в частности в авиационной и космической технике, и к способу их получения. Описан термостойкий полимерный композиционный материал, содержащий силоксановый каучук в качестве матрицы и многостенные углеродные нанотрубки (УНТ) в качестве наполнителя в количестве 0,1-1,0 мас.ч. на 100 г мас.ч. матрицы, при этом материал обладает термостойкостью: изменение массы при 400°С не более 3,93%, и физико-механическими свойствами: модуль упругости при растяжении 0,93-3,63 МПа при относительном удлинении 330-505%. Также описан способ получения полимерного композиционного материала. Технический результат: создание нового полимерного композиционного материала с повышенной термостойкостью и улучшенными механическими свойствами на основе силоксанового каучука в качестве матрицы и углеродных нанотрубок в качестве наполнителя. 2 и 4 з.п. ф-лы, 9 ил., 1 табл., 8 пр.

ВСТРОЕННЫЕ СИЛИКОН-ГИДРОГЕЛЕВЫЕ КОНТАКТНЫЕ ЛИНЗЫ

Изобретение относится к встроенным силикон-гидрогелевым контактным линзам, включающим силикон-гидрогелевый материал и гидрофобную вставку. Силикон-гидрогелевый материал содержит повторяющиеся звенья по меньшей мере одного первого полисилоксан-винилового сшивателя, включающего гидрофилизированные силоксановые звенья, каждое из которых содержит один метильный заместитель и один органический радикал, содержащий не менее одного донора Н-связи, при этом содержание указанного по меньшей мере одного донора Н-связи составляет не менее 0,8 мэкв/г по отношению к молекулярной массе указанного по меньшей мере одного первого полисилоксан-винилового сшивателя, и повторяющиеся звенья по меньшей мере одного гидрофильногго винилового мономера. Вставка состоит из сшитого полимерного материала, в котором мольная доля повторяющихся акриловых звеньев составляет не менее 55%, и мольная повторяющихся звеньев по меньшей мере одного винилового сшивающего реагента составляет не менее 6%. Указанные линзы не подвержены ...

СИЛОКСАНОВЫЕ МАТЕРИАЛЫ ДЛЯ ВКЛАДКИ С ВЫСОКИМ ПОКАЗАТЕЛЕМ ПРЕЛОМЛЕНИЯ ДЛЯ СОДЕРЖАЩИХ ВНЕДРЕННЫЙ ЭЛЕМЕНТ КОНТАКТНЫХ ЛИНЗ

Изобретение относится к вкладке для внедрения в силикон-гидрогелевую контактную линзу. Предложена вкладка для внедрения в силикон-гидрогелевую контактную линзу, содержащая сшитый полимерный материал, который содержит: (1) повторяющиеся звенья указанного по меньшей мере одного винил-функционализированного полисилоксана, который содержит по меньшей мере две винильные группы, каждая из которых непосредственно присоединена к одному атому кремния, и по меньшей мере 15% по молям силоксановых звеньев, каждое из которых содержит по меньшей мере один фенильный заместитель; (2) повторяющиеся звенья по меньшей мере одного арилакрилового мономера и (3) повторяющиеся звенья по меньшей мере одного винилового сшивающего средства, где сумма количеств компонентов (1) и (2) сшитого полимерного материала составляет по меньшей мере 70% по весу относительно общего веса сшитого полимерного материала, где сшитый полимерный материал в сухом состоянии характеризуется температурой стеклования более 28°C, где сшитый ...

СПОСОБ ПОЛУЧЕНИЯ МОДИФИЦИРОВАННОГО ДИЕНСОДЕРЖАЩЕГО КАУЧУКА, КАУЧУК И РЕЗИНОВАЯ КОМПОЗИЦИЯ НА ЕГО ОСНОВЕ

Изобретение относится к способам получения каучука растворной полимеризацией. Предложен способ получения каучука, включающему (со)полимеризацию, по меньшей мере, одного диенового мономера, и, необязательно, по меньшей мере, одного винилароматического мономера, и винилкремниевого соединения в присутствии функционализирующего литиевого инициатора, и модификацию получаемого (со)полимера полифункциональным кремнийсодержащим агентом. Функционализирующий литиевый инициатор получают взаимодействием литийорганического соединения, вторичного амина и диенсодержащего соединения. Также предложены каучуки, полученные указанным способом, резиновые композиции и резины на их основе, полуфабрикаты и шины, включающие подобный каучук. Технический результат – предложенный способ позволяет получать резиновые композиции и резины на их основе, характеризующиеся улучшенным комплексом гистерезисных свойств. 7 н. и 33 з.п. ф-лы, 3 табл., 11 пр.

ОТВЕРЖДАЕМАЯ ОРГАНОПОЛИСИЛОКСАНОВАЯ КОМПОЗИЦИЯ И ПОЛУПРОВОДНИКОВОЕ УСТРОЙСТВО

... 1. Отверждаемая органополисилоксановая композиция, включающая: ! (A) органополисилоксан следующей усредненной структурной формулы: ! R1 aSiO(4-a)/2, ! (в которой R1 обозначает незамещенные или замещенные галогеном одновалентные углеводородные группы; однако в одной молекуле по меньшей мере две группы, обозначенные R1, представляют собой алкенильные группы, и по меньшей мере 30 мол.% от всех групп, обозначенных R1, представляют собой арильные группы; и «а» представляет собой число в диапазоне от 0,6 до 2,1); ! (B) органополисилоксан, который содержит в одной молекуле по меньшей мере два связанных с кремнием атома водорода и по меньшей мере 15 мол.% от всех связанных с кремнием органических групп в форме арильных групп; ! (C) органополисилоксан с разветвленной цепью, имеющий следующую усредненную формулу блока: ! (R2SiO3/2)b(R2 2SiO2/2)c(R2 3SiO1/2)d(SiO4/2)e(XO1/2)f, ! (в которой каждый R2 независимо обозначает алкильную группу, алкенильную группу, арильную группу или эпоксисодержащую органическую ...

ЦИКЛОАЛИФАТИЧЕСКАЯ СМОЛА, СПОСОБ ЕЕ ПОЛУЧЕНИЯ И ЕЕ ПРИМЕНЕНИЕ В ВЫСОКОУСТОЙЧИВОМ ПОКРЫТИИ

КОМПОЗИЦИЯ И СПОСОБ ПОЛУЧЕНИЯ КРЕПИРОВАННОЙ БУМАГИ И ПОЛУЧЕНИЕ КРЕПИРОВАННОЙ БУМАГИ С ИХ ИСПОЛЬЗОВАНИЕМ

ИСПОЛЬЗОВАНИЕ ПОЛИМЕРИЗУЕМЫХ СМОЛ, ХАРАКТЕРИЗУЮЩИХСЯ НИЗКИМ ГАЗОВЫДЕЛЕНИЕМ В ВАКУУМЕ, ДЛЯ ИЗГОТОВЛЕНИЯ КОМПОЗИТНЫХ МАТЕРИАЛОВ, ПРЕДНАЗНАЧЕННЫХ ДЛЯ ИСПОЛЬЗОВАНИЯ В КОСМОСЕ

... 1. Применение, по меньшей мере, одной полимеризуемой смолы R1, выбираемой из группы, состоящей из эпоксидированных полибутадиеновых смол, эпоксидированных полиизопреновых смол, эпоксидированных полисилоксановых смол, эпоксидированных триглицеридных смол и эпоксидированных смол простых полиэфиров, и характеризующейся в неполимеризованном состоянии: ! - величиной общей потери массы (ОПМ), меньшей, чем 10%, величиной восстановленной потери массы (ВПМ), меньшей, чем 10%, и величиной собранного летучего конденсируемого материала (СЛКМ), меньшей, чем 1%, согласно определению в соответствии со стандартом ECSS-Q-70-02A Европейского космического агентства; и ! - эпоксидной эквивалентной массой (ЭЭМ) в диапазоне от 100 до 600 г/моль; ! для изготовления композитного материала, предназначенного для использования в космосе. ! 2. Применение по п.1, где смолой R1 является эпоксидированная полибутадиеновая смола. ! 3. Применение по п.2, где эпоксидированная полибутадиеновая смола включает форполимеры, ...

СПОСОБ ПОЛУЧЕНИЯ КОМПОЗИЦИОННЫХ ЧАСТИЦ

... 1. Способ получения композиционных частиц, отличающийся тем, что ! α) одно или несколько соединений кремния общей формулы ! , ! в которой ! R обозначает необязательно замещенный алкильный или арильный остаток с 1-20 атомами углерода или атом водорода, ! R1 обозначает необязательно замещенный углеводородный остаток или атом водорода и ! n обозначает число от 1 до 4, или ! β) один или несколько продуктов конденсации соединений кремния формулы (1) ! подвергают конденсации в растворителе или смеси нескольких растворителей в присутствии одного или нескольких растворимых полимеров, в качестве которых используют полимеры сложных виниловых эфиров с 6-15 мас.% этиленово ненасыщенных карбоновых кислот и необязательно 0,3-2 мас.% этиленово ненасыщенных силанов, полимеры сложных виниловых эфиров с 0,3-2 мас.% этиленово ненасыщенных силанов, полимеры (мет)акрилатов с 6-15 мас.% этиленово ненасыщенных карбоновых кислот и необязательно 0,3-2 мас.% этиленово ненасыщенных силанов или полимеры (мет)акрилатов ...

СМАЗОЧНОЕ ПОКРЫТИЕ ДЛЯ МЕДИЦИНСКОГО КОНТЕЙНЕРА

... 1. Смазочное покрытие для медицинского контейнера, содержащее сшитую смазочную композицию, включающую смесь инертного силикона с химически активным силиконом, где химически активный силикон содержит смесь силикона на виниловой основе и силикона на акрилатной основе.2. Смазочное покрытие по п. 1, где содержание инертного силикона составляет от 80 масс.% до 90 масс.% относительно общей массы смазочной композиции.3. Смазочное покрытие по любому из пп. 1 или 2, где содержание силикона на виниловой основе в смазочной композиции составляет от 8 масс.% до 15 масс.%, а содержание силикона на акрилатной основе в смазочной композиции составляет от 2 масс.% до 5 масс.%.4. Смазочное покрытие по п. 3, где содержание силикона на виниловой основе в смазочной композиции составляет 10 масс.%, а содержание силикона на акрилатной основе в смазочной композиции составляет 3 масс.%.5. Смазочное покрытие по п. 1, где инертный силикон представляет собой полидиметилсилоксан.6. Смазочное покрытие по п. 1, где силикон ...

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Siloxanhaltiges Gießharzsystem

VERFAHREN ZUM HYDROPHOBIEREN VON LEDER UND PELZFELLEN MIT KAMMARTIG CARBOXYLFUNKTIONALISIERTEN POLYSILOXANEN

ORGANOPOLYSILOXANE UND DIESE ENTHALTENDE AUSHAERTBARE ORGANOPOLYSILOXANZUBEREITUNG

STABILISIERTE PIGMENTIERTE POLYCARBONAT-ZUSAMMENSETZUNG

Polymer Zusammensetzung

Photohärtbare flüssige Silikonkautschukzusammensetzungen zur Herstellung einer Masterform

Raumtemperaturhärtbare Organopolysiloxanzusammensetzungen und Automobilteile

CARBINOLFUNKTIONELLE SILIKONHARZE ODER ANHYDRIDFUNKTIONELLE SILIKONHARZE ENTHALTENDE FORMMASSEN

Zu Elastomeren haertende Organopolysiloxane

Durch Michael Additionsreaktion härtbare Zusammensetzungen

Gegenstand der Erfindung sind additionsvernetzbare Zusammensetzungen Z, die eine DOLLAR A Komponente A, die mindestens eine aktivierte Methylengruppe, Amino-, Carbinol- oder Thiolfunktion als Michael-Donor trägt, DOLLAR A sowie eine DOLLAR A Komponente B, die mindestens einen Rest der allgemeinen Formel II DOLLAR A IDENTICAL Si-CR·2·¶2¶-A-D-C DOLLAR A aufweist, enthalten, wobei DOLLAR A R·2· Wasserstoff oder Kohlenwasserstoffrest mit 1 bis 12 Kohlenstoffatomen, dessen Kohlenstoffkette durch nicht benachbarte Sauerstoff-, Schwefel- oder NR·3·-Gruppen unterbrochen sein kann, DOLLAR A R·3· Wasserstoff oder Kohlenwasserstoffrest mit 1 bis 12 Kohlenstoffatomen, DOLLAR A A Sauerstoff, Schwefel, =NR·3· oder =N- (D-C), DOLLAR A D eine Carbonylgruppe und DOLLAR A C eine ethylenisch ungesättigte Gruppe bedeuten.

Deckschichtzusammensetzung, Alkali-entwicklerlösliche Deckschichtfolie mit der Zusammensetzung und Musterbildungsverfahren mit Hilfe damit

Feuchtigkeitshärtende Beschichtungsmittel auf der Basis aprotischer Lösemittel enthaltend Bindemittel mit Alkoxysilangruppen und deren Verwendung

Die Erfindung betrifft feuchtigkeitshärtende Beschichtungsmittel auf Basis aprotischer Lösemittel, enthaltend (A) mindestens ein Bindemittel mit Alkoxysilangruppen und (B) mindestens einen Vernetzungskatalysator, dadurch gekennzeichnet, dass es als Bindemittel (A) mindestens ein Polyacrylat und/oder Polymethacrylat, das erhältlich ist unter Verwendung eines oder mehrerer ethylenisch ungesättigter Monomerer (a1) der Formel (I) $F1 mit R = Wasserstoff oder Methylrest, R' = Wasserstoff, Alkyl oder Cycloalkyl, R" = Alkyl, Cycloalkyl, Aryl, oder Aralkyl, wobei die Kohlenstoffkette durch nicht benachbarte Sauerstoff-, Schwefel- oder NRa-Gruppen unterbrochen sein kann, mit Ra = Alkyl, Cycloalkyl, Aryl oder Aralkyl, x = 0 bis 2, und als Vernetzungskatalysator mindestens einen phosphor- und stickstoffhaltigen Katalysator (B), enthält. Gegenstand der vorliegenden Erfindung ist außerdem ein Verfahren zur Herstellung einer Mehrschichtlackierung unter Verwendung dieser Beschichtungsmittel, insbesondere ...

Automotive protectant compositions with improved vertical cling

The present invention relates generally to compositions, methods of use and kits for use as an automotive protectant composition and/or automotive cleaning composition. The protectant composition and/or cleaning composition comprises at least one surfactant and at least one rheology modifier, at least one silicone component, and water. The composition also optionally comprise, pH adjusters, builders, alkalinity sources, wetting agents, spreading agents, UV absorbers. The protectant composition has a viscosity of about 4000 to 6000 cps and exhibits a Vertical Cling parameter of between 1 and about 7 at a temperature of about 250C on automotive surfaces to which the compositions are applied.

Organosil oxane compositions

Fixing method and device

Radiation curable silicone release compositions and coated substrates

A radiation-curable silicone release composition is described which comprises (A) a mixture of organopolysiloxanes characterized by the formula (I): RSi(CH 3 ) 2 -O-(Si(CH 3 ) 2 O) n (Si(CH 3 )(R)O) m Si(CH 3 ) 2 R wherein the mixture comprises (A-1) from about 25 % to 95 % by weight of at least one organopolysiloxane characterized by formula (I) wherein each R is -R 1 -O(O)C-C(R 2 )=CH 2 , R 1 is a hydrocarbylene group, R 2 is hydrogen or a methyl or ethyl group, m is a number from about 1 to about 15, and n is a number from about 50 to about 300, and (A-2) from about 5 % to 75 % by weight of at least one other organopolysiloxane characterized by formula (I) wherein R is -R 1 -OCH 2 CH(OH)-CH 2 O(O)C-C(R 2 )=CH 2 , R 1 is a hydrocarbylene group, R 2 is hydrogen or a methyl or ethyl group, m is a number from about 1 to about 25, and n is a number from about 50 to about 300, and (B) from 0 % to about 5 % by weight of a photoinitiator. A method of producing silicone release-coated substrates ...

Alkenyl-substituted crown ethers

New C-substituted crown ethers such as are made by reacting a 1,2-diol (chain length m + 4) with ClCH2-(CH2-O-CH2-)n+1CH2Cl. These compounds have a stronger affinity for secondary amines than for tertiary amines and therefore may be used to separate mixtures, especially when attached to polysiloxane backbones or substrates via their unsaturated bond.

Extenders for organosiloxane compositions

Personal care compositions containing siloxane based polyamide elastomers

A fluid blood coagulation promoter

What is disclosed is a composition of matter useful in expediting the coagulation of whole blood. The coagulation promoter is a polysiloxane which contains at least one hydroxy functional or carboxylic functional monovalent hydrocarbon radical bonded to a silicon atom.

Curable compositions

FLAME RETARDANT COMPOSITION

... 1482220 Flame retardant alkenyl aromatic polymer compositions GENERAL ELECTRIC CO 11 Sept 1974 [18 Oct 1973] 39633/74 Heading C3P A flame retardant composition comprises (a) an alkenyl aromatic polymer; (b) a flame retardant additive; and (c) a minor amount of a diorganopolysiloxane polymer gum wherein the organo substituents therein are selected from alkyl, aryl and vinyl radicals and mixtures thereof. Preferred alkenyl aromatic polymers are styrene polymers containing at least 50 wt. per cent styrene, such as 50 : 50 w./w. styrene/ butadiene copolymer, or an A.B.S. polymer. In tne examples, component (c) is a methyl phenyl vinyl polysiloxane. Preferred components (b) are halogenated polycarbonates, especially of the formula wherein n has an average value of 3 to 7. Component (c) preferably also contains an antimony compound such as antimony oxide.

VERFAHREN ZUR HERSTELLUNG VON SCHAUMSTOFFEN

HITZEERHÄRTBARE SILICONE COMPOSITION

AMINOPLAST-FORMMASSEN FÜR ERZEUGNISSE VERBESSERTER FLEXIBILITÄT

HARDENABLE ONE ORGANOPOLYSILOXANZUSAMMENSETZUNG

CARBINOLFUNKTIONELLE SILICONE RESINS OR ANHYDRIDE-FUNCTIONAL OF SILICONE RESINS CONTAINING MOLDING MATERIALS

USE OF LIGHT-ACTIVATE-CASH, HARDENABLE ONES SILICONE COMPOSITIONS FOR THE PRODUCTION OF THICK-WALLED FORM ARTICLES OR THICK-WALLED COATINGS

PROCEDURE FOR LUBRICATING INJEKTIONSNADELN WITH RADIATIONHARDENABLE SILICONE MATERIAL

HARDENABLE SILICONE COMPOSITION AND HARDENED PRODUCT OF IT

INTERLACE-CASH MASSES ON THE BASIS OF ORGANOSILICIUMVERBINDUNGEN

SILICONE COATING COMPOSITIONS

POLYMER COMPOSITION WITH METAL ALKOXIDE CONDENSATION PRODUCT, ORGANIC SILANE CONNECTION AND BORON CONNECTION

SILIKONE WITH IMPROVED SURFACE PROPERTIES AND HARDENABLE ONE SILICONE COMPOSITIONS FOR THE PRODUCTION OF THESE SILKONE

LAMINATED SILICONE SUBSTRATE, PROCEDURE FOR ITS PRODUCTION, SILICONE RESIN COMPOSITION FOR THE PRODUCTION OF THE LAMINATED SILICONE SUBSTRATE AND LED DEVICE

AMINOPLASTERZEUGNISSE OF IMPROVED FLEXIBILITY

H�RTBARE EPOXY RESIN COMPOSITION

SACCHARIDE-CONTAINING FUNCTIONAL ONES ORGANOPOLYSILOXANE AND PROCEDURES FOR THEIR PRODUCTION

HARDENABLE SILICONE COMPOSITION AND ELECTRONIC COMPONENTS

HARDENABLE SILICONE COMPOSITION AND YOUR USE AS ADHESIVE

HARDENABLE POLYSILOXANZUSAMMENSETZUNGEN, THE NORBONYL FUNCTIONAL GROUPS CONTAINING

COATING PROCESS WITH DOUBLE HARDENING BY PRECIPITATION FOR ARTICLES WITH SCHATTENGEBIETEN.

ORGANOPOLYSILOXANHARZMASSE UND IHRE VERWENDUNG ALS HAFTVERBESSERER

AQUEOUS DISPERSIONS OF POLYSILOXANEN.

BY ELIMINATION FROM WATER TO AN ELASTOMER INTERCONNECTION WAESSRIGE DISPERSION ON BASIS OF FUNKTIONALISIERTEN SILICONE OILS.

PROCEDURE FOR THE HYDROPHOBIEREN OF LEATHER AND FUR SKINS WITH COMBLIKE CARBOXYLFUNKTIONALISIERTEN POLYSILOXANEN

USE OF EMULSIFIED ADHESION MEDIATORS AS PRIMING FOR DICHTUNGSMATERIALEN, ADHESIVES AND COATINGS

HARDENABLE FLUORELASTOMETRIC COMPOSITIONS CONTAINING HYDROSILOXANE OR HYDROSILAZANE

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

AQUEOUS HARDENABLE ONES SILANE/CPOLYMER COMPOSITIONS

Optical transparent resin and electronic element formed using same

The present invention relates to an optical transparent resin comprising: 1) a polyorganosiloxane resin represented by chemical formula 1 above; and 2) at least one light initiator, the optical transparent resin having a refractive index of 1.41-1.55, and to an electronic element formed by using the optical transparent resin.

SILICONE ADHESIVE

Method of thermally processing elastomeric compositions and elastomeric compositions with improved processability

Use of hydrophobic epoxide resin system for encapsulation of a instrument transformer

Disclosed is the use of a curable composition for padding-free encapsulation of instrument transformers comprising (a) a cycloaliphatic epoxy resin, (b) a polyoxyalkylene diglycidylether (c) an OH-terminated polysiloxane, (d) a cyclic polysiloxane and (e) a non-ionic, fluoroaliphatic surface-active reagent, (f) a filler, (g) a hardener selected from anhydrides, (h) a curing accelerator selected from accelerators for anhydride curing of epoxy resins.

Pigmented two-component protective coating

The invention relates to a two-component protective coating, comprising mineral pigments, an epoxy siloxane binder component, and an amine hardener. The two-component protective coating comprises initially separated components A and B, wherein component A comprises (a1) x wt % of inorganic pigments, wherein x = 30 to 70; (a2) 10 to 50 wt % of at least one epoxy siloxane, and (a3) 0 to 40 wt % of an organic solvent and wherein component B comprises (b1) at least one amine hardener and (b2) optionally at least one organic solvent.

Static resistant polycarbonate compositions

FLAME RETARDANT COMPOSITION

Silicone hydrogels having improved curing speed and other properties

The present invention relates to: to a silicone polymer formed from reactive components containing (i) at least one silicone component and (ii) 2-hydroxyethyl acrylamide; a silicone hydrogel containing such silicone polymer; a biomedical device (e.g., a contact lens) containing such polymer; and a biomedical device formed from such hydrogel.

Organosiloxane Compositions

Disclosed is a room temperature curable organopolysiloxane composition which has strength in an uncured state of at least 600 Pa measured after one minute, and wherein the organopolysiloxane composition comprises: a) from 20 to 45% by weight of an organopolysiloxane polymer having a viscosity of at least 1000mPa.s at 2500C and not less than two silicon-bonded hydroxyl groups and/or silicon bonded hydrolysable groups; b) a precipitated calcium carbonate filler; c) from 0.1 to 3% by weight of a suitable catalyst; d) from 1 to 10% by weight of a cross-linker adapted to react with component (a) selected from a suitable silane or short chain organopolysiloxane having at least two and preferably three or more hydroxyl and/or otherwise hydrolysable groups wherein the hydrolysable groups in component (d) may comprise acyloxy groups; alkoxy groups and alkenyloxy groups, catalysed with component (c); e) one or more rheology modifiers; f) 0 to 10% by weight of the composition of one or more extenders ...

Epoxy siloxane coating compositions

Epoxy-polysiloxane based coating and flooring compositions exhibiting improved flexibility, and excellent weatherability and corrosion resistance after curing are described. The epoxy-polysiloxane polymer coating composition may be prepared by combining a polysiloxane, an epoxide resin material and a cure system including a blend of compounds selected from a dialkoxy functional aminosilane, a trialkoxy functional aminosilane, and an amino functional polysiloxane resin, where the blend has an average alkoxy functionality value of 2.0 to 2.8.

Composition for organic electronic element encapsulant, and encapsulant formed by using same

A composition for an encapsulant, according to one embodiment of the present application, comprises 1) a silicone resin, 2) one or more types of moisture absorbent, 3) one or more types of photoinitiator, 4) one or more types of filler, and 5) a reactive silicone oligomer.

Curable polymethylsilsesquioxane composition

Polydimethylsiloxane-containing polymer blends

Curable compositions containing a polysiloxane additive

POLYMERIZING POLYORGANOSILOXANES

Crosslinkable polyorganosiloxane composition

SILICONE COATING COMPOSITION

CURABLE SILICONE COMPOSITIONS HAVING ENHANCED CURE-THROUGH-VOLUME

A photocurable silicone composition which includes an additive which provides cure-through-volume of the overall composition. The additive is desirably a curable amino silyl-terminated polyorganosiloxane.

A PROCESS FOR THE PREPARATION OF MOISTURE-CURABLE, POLYETHER URETHANES WITH TERMINAL CYCLIC UREA/REACTIVE SILANE GROUPS

... ²²²A process for preparing a moisture-curable, polyether urethane containing ²terminal cyclic urea/reactive silane groups by reacting at an NCO:OH ²equivalent ratio of 1.5:1 to 2.5:1 a) a hydroxyl component containing i) a ²polyether containing two hydroxyl groups and one or more polyether segments, ²wherein the polyether segments have a number average molecular weight of at ²least 3000 and a degree of unsaturation of less than 0.04 milliequivalents/g, ²and ii) a polyether containing one hydroxyl group and one or more polyether ²segments having a number average molecular weight of 1000 to 15,000, with b) ²an isocyanate component containing i) a compound containing two isocyanate ²groups, and ii) a compound containing one isocyanate group, and subsequently ²reacting this reaction product at an equivalent ratio of isocyanate groups to ²isocyanate-reactive groups of 0.8:1 to 1.1:1 with c) a compound containing an ²aspartate group and a reactive silane group to form an intermediate polyether ...

AQUEOUS COATING AGENT COMPOSITION

The present invention provides an aqueous coating agent composition which does not contain an organic tin compound and forms a coating film that has good lubricity, excellent bondability (adhesiveness) and excellent wear resistance. This aqueous coating agent composition contains (A) a polydiorganosiloxane which has a viscosity (at 25°C) of 50 to 100,000,000 mPa·s, while having both terminals blocked with hydroxyl groups, (B) a polyorganohydrogen siloxane which has at least three hydrogen atoms in each molecule, (C) a zinc compound which serves as a curing catalyst, (D) an organic compound having at least one of a primary amino group and a secondary amino group and/or a polyorganosiloxane, (E) an adhesion improving component and (F) spherical fine particles.

OPTICAL GLASS FIBRE HAVING A SYNTHETIC RESIN CLADDING AND METHOD OF MANUFACTURING SAME

The invention provides an optical glass fibre having a synthetic resin cladding and a method of manufacturing same, in which the first layer of the synthetic resin cladding is formed from a curable polysiloxane composition. The curing rate is increased by the presence of acrylate groups. The refractive index (exceeding 1.46) and the glass transition temperature (lower than -50.degree.C) can be adjusted by the ratio of the dimethyl siloxane groups, methyl phenyl siloxane groups and diphenyl siloxane groups present. The curing rate can furthermore be increased by the addition of monomeric acrylate compounds.

METHOD OF PREPARING A PLATINUM CATALYST INHIBITOR

PRINTABLE, ADHESIVE RELEASE COMPOSITION

An adhesive release composition containing specific amounts of an organopolysiloxane bearing oxyalkylene groups and alkenyl groups, an organohydrogenpolysiloxane, and a platinum-type catalyst is characterized by the formation, on various base surfaces, of a release surface having an excellent printability and a stable release force. For example, a roll of pressure sensitive adhesive tape of this invention can be easily unrolled, durably adhered to an article and clearly printed with ink on its adhesivereleasing surface which bears the release composition of this invention.

CONCRETE JOINT SEALANT HAVING IMPROVED ADHESION

A silicone sealant composition which bonds to dolomite containing concrete after exposure to moisture is obtained by adding a silicone fluid having greater than 2 mole percent epoxy functionality to a sealant of the type containing a hydroxyl endblocked polydiorganosiloxane, acetamidosilane chain extender and crosslinking agent selected from the group consisting of triacetamidosilane and aminoxysilicon compound.

COATING COMPOSITION

A coating composition comprising a reaction product of the following components: (a) at least one cyclic ether or anhydride; and (b) an alkoxysilane-functional polyacrylate, alkyd, polyester, epoxy, or a multifunctional polyol; and (c) at least one metal ester having the general formula Rm-M(OR~)n, in which M is Si, Al, Zr, or Ti, Mg, B, W. or Mo R is a hydrocarbon group of less than 10 carbon atoms or a group comprising hydrogen, carbon and oxygen of less than 20 carbon atoms, R~ is an alkyl or aryl group with less than 10 carbon atoms, m has values of 0, 1, 2 an 3 and correspondingly n is 4, 3, 2, or 1; and (d) at least one organofunctional alkoxysilane.

WETTABLE SILICONE RESIN OPTICAL DEVICES AND CURABLE COMPOSITIONS THEREFOR

METHOD FOR THE PREPARATION OF ORGANOPOLYSILOXANES HAVING (METH)ACRYLATE FUNCTIONS

La présente invention concerne un procédé de préparation de polyorganosiloxanes fonctionnalisés par des groupements (méth)acrylates, de préférence acrylates.

Siloxane-based low dielectric constant thin films using cyclo-siloxane and a method for preparing the same

Disclosed are a low-dielectric-constant thin film prepared from a silsesquioxane polymer matrix as a precursor, the silsesquioxane polymer matrix being a silsesquioxane sol prepared by adding a stereoisomer of a multireactive cyclosiloxane to an alkoxysilane, and a method for preparing the same. The disclosed low-dielectric-constant thin film retains a stable film state even at a curing temperature of ˜500° C. without being decomposed. Also, it exhibits a very uniform surface property with a low surface modulus and has such a superior coatability as to be coatable smoothly with no crack even with a thickness of 500 nm or larger. In addition, the low-dielectric-constant thin film according to the present disclosure may exhibit low dielectric property while having superior surface modulus and hardness.

Flexible-to-rigid tubing

A flexible-to-rigid tube is flexible when routed and is then rigidized to increase burst strength. According to the preferred embodiments of the present invention, the flexible-to-rigid tube is included in a cooling plate assembly for transferring heat from electronic components mounted on a circuit board. In one embodiment, the flexible-to-rigid tube (while in a flexible state) includes a polydimethylsiloxane (PDMS) or other silicone containing pendant or terminal epoxy, vinyl and/or acrylate functional groups and an initiator (e.g., a sulfonium salt photoinitiator, a free radical photoinitiator, or a thermal initiator). In another embodiment, triallyl isocyanurate (TAIC) and an initiator are incorporated into a conventional PVC-based tubing material. The flexible-to-rigid tube changes from the flexible state to a rigid state via formation of a cross-linked network upon exposure to actinic radiation or heat.

Durable Non-Fluorine Water Repellent Agent and Process for Preparing Same

The present invention provides a crosslinkable polysiloxane-containing composition and a process for treating a textile with the composition whereby desirable properties, such as water repellency and durability, are enhanced.

Use of Ionomeric Silicone Thermoplastic Elastomers in Electronic Devices

This invention relates to the use of a thermoplastic elastomer comprising at least one silicone ionomer in the formation of electronic devices.

Wafer mold material and method for manufacturing semiconductor apparatus

The invention provides a wafer mold material for collectively subjecting a wafer having semiconductor devices on a surface thereof to resin molding, wherein the wafer mold material has a resin layer containing a filler and at least any one of an acrylic resin, a silicone resin having an epoxy group, an urethane resin, and a polyimide silicone resin, and the wafer mold material is formed into a film-like shape. There can be a wafer mold material that enables collective molding (wafer molding) with respect to a wafer having semiconductor devices formed thereon, has excellent transference performance with respect to a large-diameter thin-film wafer, can provide a flexible hardened material with low-stress properties, and can be preferably used as a mold material in a wafer level package with less warp of a formed (molded) wafer.

Polyhedral oligomeric silsesquioxane compositions, methods of using these compositions, and structures including these compositions

Embodiments of the present disclosure include functionalized polyhedral oligomeric silsesquioxane compositions or mixtures, methods of using functionalized polyhedral oligomeric silsesquioxane compositions, structures including functionalized polyhedral oligomeric silsesquioxane, and the like.

Method for Producing (Hydroxymethyl)Polysiloxanes

A method for producing (hydroxymethyl)polysiloxanes of the general formula I (SiO 4/2 ) k (R 1 SiO 3/2 ) m (R 1 2 SiO 2/2 ) p (R 1 3 SiO 1/2 ) q [O 1/2 —(SiR 2 2 —X—Y—) a SiR 2 2 —CH 2 —OH] s [O 1/2 H] t   formula I, includes reacting silanol-containing organosiloxanes of the general formula II (SiO 4/2 ) k (R 1 SiO 3/2 ) m (R 1 2 SiO 2/2 ) p (R 1 3 SiO 1/2 ) q [O 1/2 H] r   formula II with cyclic or acyclic compounds that include at least one unit of the general formula III. Z—[O—CH 2 —SiR 2 2 ] n —Y   formula III

RESIN PARTICLE AND METHOD FOR PRODUCING SAME

Disclosed is a resin particle having excellent low-temperature fusibility, having a sufficiently narrow size distribution, and that is obtained using a liquid or supercritical fluid. In the resin particle (C), which comprises a microparticle (A) containing a resin (a) being coated to or adhered to the surface of a resin particle (B) that contains another resin (b), the degree of swelling of the microparticle (A) resulting from liquid or supercritical carbon dioxide (X) at a temperature less than the glass transition temperature or the melting point of the microparticle (A) is no greater than 16%, and with the resin (a) as a constituent unit, the resin particle (C) contains 0.1-50 wt % of a non-crystalline non-halogen vinyl monomer (m1) of which the solubility parameter (SP value: (cal/cm)) is 7-9. 1. A resin particle (C) comprising a microparticle (A) containing a resin (a) being coated to or adhered to the surface of a resin particle (B) containing a resin (b) , wherein the degree of swelling of the microparticle (A) resulting from liquid or supercritical carbon dioxide (X) at a temperature less than the glass transition temperature or the melting point of the microparticle (A) is no greater than 16% , and the resin (a) contains , as a constituent unit , 0.1 to 50 wt % of a non-crystalline non-halogen vinyl monomer (m1) having a solubility parameter [SP value: (cal/cm)] of 7 to 9.2. The resin particle (C) according to claim 1 , wherein the non-crystalline non-halogen vinyl monomer (m1) is at least one kind of vinyl monomer selected from a silicone-containing vinyl monomer (m11) and a branched alkyl group-containing vinyl monomer (m12) having a carbon number of 8 to 30.3. The resin particle (C) according to claim 1 , wherein the resin (a) further contains claim 1 , as a constituent unit claim 1 , 30 to 99.9 wt % of a crystalline vinyl monomer (m2).4. The resin particle (C) according to claim 1 , wherein the particle diameter of the microparticle (A) is 0.01 to 1.0 μ ...

SILICON-CONTAINING CURABLE COMPOSITION, CURED PRODUCT OF THE SILICON-CONTAINING CURABLE COMPOSITION AND LEAD FRAME SUBSTRATE FORMED OF THE SILICON-CONTAINING CURABLE COMPOSITION

A curable composition includes: 100 parts by mass of a silicon-containing polymer having a Mw of 3,000 to 100,000 obtainable by hydrolysis-condensation of an organosilane mixture including RSiX, RSiX, RRSiXand RSiX, the total of RSiXand RRSiX2 being 5 to 60 mol %, optionally a prepolymer, optionally a cyclic siloxane compound, 0.0001 to 10 parts by mass of an organic peroxide and optionally a metal catalyst, and 10 to 1,500 parts by mass of a filler, wherein Ris a C2-6 alkenyl group, Ris a C1-6 alkyl group, Rand Rare each a C1-6 alkyl group, Ris a phenyl group optionally substituted with a C1-6 alkyl group, and X is a C1-6 alkoxy group, one or more of Rto Ris a methyl group, f represents a number of 2 to 10, g represents a number of 0 to 8, and n represents 1 or 2. 2. The silicon-containing curable composition according to claim 1 , wherein Ris a methyl group in the formula (1-2) claim 1 , and Rand Rare phenyl groups optionally substituted by an alkyl group having 1 to 6 carbon atoms in the formula (1-3).3. The silicon-containing curable composition according to claim 1 , wherein Ris an alkyl group having 1 to 6 carbon atoms in the formula (1-2) claim 1 , and Ris an alkyl group having 1 to 6 carbon atoms and Ris a phenyl group optionally substituted by an alkyl group having 1 to 6 carbon atoms in the formula (1-3).4. The silicon-containing curable composition according to claim 1 , wherein the content of the component (B) with respect to 100 parts by mass of the component (A) is 10 to 200 parts by mass.6. A cured product obtainable by curing the silicon-containing curable composition according to .7. A lead frame substrate for an LED light emitting device comprising a lead frame and a resin molded body claim 1 , wherein the resin molded body is formed of the silicon-containing curable composition according to .8. An LED light emitting device apparatus using the lead frame substrate for an LED light emitting device according to .9. The silicon-containing curable ...

POLYCARBONATE-BASED RESIN COMPOSITION AND MOLDED ARTICLE THEREOF

Provided are a polycarbonate-based resin composition that brings together an excellent impact strength and excellent flame retardancy and a molded article thereof. The polycarbonate-based resin composition is a polycarbonate-based resin composition, including, with respect to 100 parts by mass of (A) a resin mixture formed of 30 to 100 mass % of (A-1) a polycarbonate-polyorganosiloxane copolymer which has a constituent unit represented by a general formula (I) and a constituent unit represented by a general formula (II), and in which an average number of repetitions of the constituent unit represented by the general formula (II) is 30 to 500, and 70 to 0 mass % of (A-2) an aromatic polycarbonate resin except the polycarbonate-polyorganosiloxane copolymer, 0.01 to 0.15 part by mass of (B) an alkali metal salt and/or alkaline earth metal salt of an organosulfonic acid, and 0.1 to 1 part by mass of (C) a mixed powder formed of polytetrafluoroethylene particles and organic polymer particles, in which: a content of a polyorganosiloxane block moiety formed of the constituent unit represented by the general formula (II) in the resin mixture (A) is 2 to 30 mass %; and the composition is free of an organohalogen-based flame retardant and an organophosphate-based flame retardant. 2. The composition according to claim 1 , comprising claim 1 , as the organosulfonic acid (B) claim 1 , an alkali metal salt claim 1 , an alkaline earth metal salt claim 1 , or both claim 1 , of a perfluoroalkanesulfonic acid.3. The composition according to claim 1 , comprising claim 1 , as the organic polymer particles of the mixed powder (C) claim 1 , particles comprising an alkyl (meth)acrylate-based copolymer.4. A molded article obtained by molding the polycarbonate-based resin composition according to .5. The composition according to claim 2 , comprising claim 2 , as the organic polymer particles of the mixed powder (C) claim 2 , particles comprising an alkyl (meth)acrylate-based copolymer.6. A ...

Curable-on-demand polysiloxane coating composition

A curable composition comprises (a) at least one polydiorganosiloxane, fluorinated polydiorganosiloxane, or combination thereof comprising reactive silane functionality comprising at least two hydroxysilyl moieties; (b) at least one polydiorganosiloxane, fluorinated polydiorganosiloxane, or combination thereof comprising reactive silane functionality comprising at least two hydrosilyl moieties; and (c) at least one photoactivatable composition that, upon exposure to radiation, generates at least one base selected from amidines, guanidines, phosphazenes, proazaphosphatranes, and combinations thereof; wherein at least one of the components (a) and (b) has an average reactive silane functionality of at least three.

Antistatic antireflection film, method for manufacturing antistatic antireflection film, polarizing plate and image display device

An antistatic antireflection film, including; a support; a hardcoat layer formed from a composition for a hardcoat layer containing at least a compound having a quaternary ammonium salt group; and a low refractive index layer formed from a composition for a low refractive index layer containing at least the following (a), (b), (c) and (d), in this order, wherein, (a) is an ethylenically unsaturated group-containing fluoropolymer, (b) is a fluorine-containing polyfunctional monomer having a surface free energy of 23 mN/m or more when a film is formed alone, four or less —CF 3 groups in a molecule, a fluorine content of 30% or more, and at least three reactive functional groups in one molecule, (c) is hollow silica fine particles having an average particle size of 10 nm to 100 nm, and (d) is a compound having a dimethylsiloxane structure.

PHOTO-CURING POLYSILOXANE COMPOSITION AND APPLICATION THEREOF

This invention relates to a photo-curing polysiloxane composition including a polysiloxane, a quinonediazidesulfonic acid ester, a methylene alkoxyaryl-containing compound as a curing agent, and a solvent for dispersing the polysiloxane, the quinonediazidesulfonic acid ester, and the methylene alkoxyaryl-containing compound. This invention also provides a protecting film made from the photo-curing polysiloxane composition, and an element containing the protecting film. 2. The photo-curing polysiloxane composition as claimed in claim 1 , wherein said methylene alkoxyaryl-containing compound is in an amount ranging from 3 to 35 parts by weight based on 100 parts by weight of said polysiloxane.3. The photo-curing polysiloxane composition as claimed in claim 1 , wherein Rrepresents hydrogen.4. The photo-curing polysiloxane composition as claimed in claim 1 , wherein X represents a C-Calkyl group.6. The photo-curing polysiloxane composition as claimed in claim 1 , wherein Rrepresents hydrogen.7. The photo-curing polysiloxane composition as claimed in claim 1 , wherein Rrepresents an alkyl group.8. The photo-curing polysiloxane composition as claimed in claim 1 , wherein said polysiloxane (A) is a copolymer obtained by subjecting a silane monomer of Formula (III) to hydrolysis and partial condensation claim 1 ,{'br': None, 'sup': a', 'b, 'sub': t', '4 t, 'Si(R)(OR)\u2003\u2003(III)'}whereint is an integer ranging from 0 to 3,{'sup': a', 'a, 'sub': 1', '10', '2', '10', '6', '15, 'Ris selected from the group consisting of hydrogen, a C-Calkyl group, a C-Calkenyl group, a C-Caryl group, an anhydride-substituted alkyl group, an oxetanyl-substituted alkyl, an oxetanyl-substituted alkoxy group, a glycidyl-substituted alkyl group, and a glycidyl-substituted alkoxy group, plural Rs being identical with or different from each other when t is 2 or 3, and'}{'sup': b', 'b, 'sub': 1', '6', '1', '6', '6', '15, 'Ris selected from the group consisting of hydrogen, a C-Calkyl group, a C- ...

EMULSIONS OF ORGANOPOLYSILOXANES HAVING ACIDIC AND BASIC GROUPS AND THE PRODUCTION THEREOF

Organopolysiloxanes containing both acidic and basic groups are prepared by reacting oganopolysiloxanes with primary or secondary amino groups with a stoichiometric deficiency of isocyanates containing sulfonyl-group-containing electron withdrawings groups in the presence of acidic or basic moderators. 111.-. (canceled)13. The method of claim 12 , wherein from 0.1 to 0.8 mol of isocyanate groups are present per mol of amino groups in (1).14. The method of claim 12 , wherein from 0.5 to 0.8 mol of isocyanate groups are present per mol of amino groups in (1).16. The method of claim 15 , wherein from 0.1 to 0.8 mol of isocyanate groups are present per mol of amino groups in (1).17. The method of claim 15 , wherein from 0.5 to 0.8 mol of isocyanate groups are present per mol of amino groups in (1).28. The method of claim 12 , wherein the acidic or basic moderators (3) are removed from the (4a) reaction products from (1) and (2) obtained in the first step claim 12 ,where organopolysiloxanes (4b) that are liquid at 25° C. and 1020 hPa and have a viscosity of from 100 to 1,000,000 Pa·s (25° C.) or are elastomer-like organopolysiloxanes are obtained, where the organopolysiloxanes have, as basic groups, primary and/or secondary amino groups (—NH—) and, as acidic groups, those of the formula X—NH—CO—N═.29. The method of claim 13 , wherein the acidic or basic moderators (3) are removed from the (4a) reaction products from (1) and (2) obtained in the first step claim 13 ,where organopolysiloxanes (4b) that are liquid at 25° C. and 1020 hPa and have a viscosity of from 100 to 1,000,000 Pa·s (25° C.) or are elastomer-like organopolysiloxanes are obtained, where the organopolysiloxanes have, as basic groups, primary and/or secondary amino groups (—NH—) and, as acidic groups, those of the formula X—NH—CO—N═.304a. The method of claim 14 , wherein the acidic or basic moderators (3) are removed from the () reaction products from (1) and (2) obtained in the first step claim 14 ,where ...

POLYHYDROXY CURABLE FLUOROELASTOMER COMPOSITIONS

Disclosed herein is a curable composition comprising a polyhydroxy curable fluoroelastomer, a polyhydroxy curative, a cure accelerator and an unsaturated metal compound process aid comprising a siloxane having at least one vinyl or allyl group bonded to a silicon atom. Such curable compositions have a lower Mooney viscosity than do similar compositions absent the process aid. 1. A curable fluoroelastomer composition comprising:A) a polyhydroxy curable fluoroelastomer;B) a polyhydroxy curative;C) a cure accelerator; andD) an unsaturated metal compound process aid comprising a siloxane having at least one vinyl or allyl group bonded to a silicon atom.2. The curable composition of wherein said unsaturated metal compound process aid is 1 claim 1 ,5-divinyl-3 claim 1 ,3-diphenyl-1 claim 1 ,1 claim 1 ,5 claim 1 ,5-tetramethyltrisiloxane.3. The curable composition of wherein said unsaturated metal compound process aid is 1 claim 1 ,3-divinyl-1 claim 1 ,3-diphenyl-1 claim 1 ,3-dimethyldisiloxane.4. The curable composition of wherein said unsaturated metal compound process aid is 1 claim 1 ,5-divinylhexamethyltrisiloxane.5. The curable composition of wherein said unsaturated metal compound process aid is 1 claim 1 ,3-divinyltetraphenyldisiloxane.6. The curable composition of wherein said unsaturated metal compound process aid is vinyl terminated polydimethylsiloxane.7. The curable composition of wherein said unsaturated metal compound process aid is vinyl terminated diphenylsiloxane-dimethylsiloxane copolymer.8. The curable composition of wherein said unsaturated metal compound process aid is vinylmethylsiloxane homopolymer.9. The curable composition of wherein said unsaturated metal compound process aid is vinyldiphenylethoxysilane.10. The curable composition of wherein said unsaturated metal compound process aid is allyltrimethoxysilane.11. The curable composition of wherein said unsaturated metal compound process aid is vinyltriphenoxysilane. This application claims the ...

Hydrosilylation Cured Silicone Resins Plasticized By Organophosphorous Compounds

In various embodiments, provided are novel curable silicone compositions; films and adhesives comprising one or more cured products of said compositions, the films and adhesives exhibiting properties of mechanical flexibility and low flammability. Additionally, the films and adhesives may exhibit one or more of high transparency, low haze, and high refractive index. 2. A silicone composition according to claim 1 , wherein the silicone resin of (A) has formula (III):{'br': None, 'sup': 1', '2', '2', '1, 'sub': 2', '1/2', 'w', '2', '2/2', 'x', '3/2', 'y', '4/2', 'z, '(RRSiO)(RSiO)(RSiO)(SiO)\u2003\u2003(III)'}{'sup': 1', '2', '1, 'sub': 1', '10', '6', '20, 'wherein each Ris independently selected from Cto Calkyl, Cto Caryl, or halogen-substituted derivates thereof; each Ris independently selected from Ror an alkenyl group, provided that the resin has an average of at least two silicon-bonded alkenyl groups per molecule; and wherein w, x, y, and z are mole fractions with w=0 to 0.8, x=0 to 0.6, y=0 to 0.99, z=0 to 0.35; and wherein w+x+y+z=1, y+z/(w+x+y+z)=0.2 to 0.99, and w+x/(w+x+y+z)=0.01 to 0.8.'}3. A silicone composition according to claim 2 , wherein y+z/(w+x+y+z)=0.5 to 0.95.4. (canceled)5. A silicone composition according to claim 2 , wherein w+x/(w+x+y+z)=0.05 to 0.5.6. A silicone composition according to claim 1 , comprising from 50 to 99% (w/w) of the hydrosilylation-curable silicone composition of (A).7. A silicone composition according to claim 1 , comprising from 2 to 15% (w/w) of the at least one organophosphate compound of (B).8. (canceled)9. A silicone composition according to claim 1 , wherein at least 60 mol % of the alkyl or aryl groups in the silicone resin of (A) are the same as the groups Rin the organophosphate compound of (B).10. A silicone composition according to claim 2 , wherein the organosilicon compound of (A) is selected from (ViMeSiO)(PhSiO) claim 2 , (ViMeSiO)(PhSiO) claim 2 , (ViMeSiO)(MeSiO)(PhSiO) claim 2 , (ViMeSiO)(PhSiO)(SiO) ...

PROCESS FOR PRODUCING COMPATIBILIZED RESIN, THERMOSETTING RESIN COMPOSITION, PREPREG, AND LAMINATE

Provided are a process for producing a compatibilized resin including reacting a cyanate compound, a siloxane resin having a hydroxyl group at an end thereof, and an epoxy resin at a specified rate of reaction; a thermosetting resin composition containing (A1) a compatibilized resin produced by the foregoing process or (A2) a thermosetting resin obtained by reacting a cyanate compound and a siloxane resin having a hydroxyl group at an end thereof at a specified rate of reaction, and (B) fused silica having been subjected to a surface treatment with a trimethoxysilane compound; and a prepreg, a laminate, and a wiring board each using the same. The foregoing thermosetting resin composition is excellent in terms of all of low thermal expansion, adhesiveness to copper foil, heat resistance, flame retardancy, copper-clad heat resistance (T-300), dielectric characteristics, and drillability, achieves the high density and high reliability of wiring boards required at present, and can be widely used for production of electronic appliances and the like. 15.-. (canceled)7. A thermosetting resin composition comprising (A1) a compatibilized resin produced by the process according to and (B) fused silica.12. A prepreg obtained by impregnating or coating a base material with the thermosetting resin composition according to and then bringing it into a B-stage.13. A laminate formed using the prepreg according to .15. A prepreg obtained by impregnating or coating a base material with the thermosetting resin composition according to and then bringing it into a B-stage.16. A laminate formed using the prepreg according to . The present invention relates to a process for producing a compatibilized resin from which a thermosetting resin composition which is excellent in terms of low thermal expansion, adhesiveness to copper foil, heat resistance, flame retardancy, copper-clad heat resistance (T-300), dielectric characteristics, and drillability is obtained, a thermosetting resin ...

CURABLE-ON-DEMAND COMPOSITION COMPRISING DUAL REACTIVE SILANE FUNCTIONALITY

A curable composition comprises (a) at least one inorganic or organic compound comprising reactive silane functionality comprising at least one hydrosilyl moiety; (b) at least one inorganic or organic compound comprising reactive silane functionality comprising at least one hydroxysilyl moiety, the hydroxysilyl moiety optionally being generated in situ by hydrolysis of at least one hydrosilyl moiety; and (c) at least one photoactivatable composition that, upon exposure to radiation, generates at least one base selected from amidines, guanidines, phosphazenes, proazaphosphatranes, and combinations thereof; with the proviso that, when component (a) is an organic polymer, then component (b) is different from component (a) and is not generated in situ by hydrolysis of component (a). 4. The composition of claim 2 , wherein said A is a polymeric radical; each said G is independently selected from a covalent bond claim 2 , oxy claim 2 , diorganosiloxy claim 2 , diheteroorganosiloxy claim 2 , alkylene claim 2 , arylene claim 2 , heteroalkylene claim 2 , heteroarylene claim 2 , cycloalkylene claim 2 , heterocycloalkylene claim 2 , and combinations thereof; each said R is independently alkyl; each said p is an integer of 1; and/or said m is an integer of 1 to 50.5. The composition of claim 4 , wherein said A is a polymeric radical selected from polysiloxane claim 4 , polyacrylate claim 4 , polyolefin claim 4 , polyether claim 4 , polyester claim 4 , fluorinated polysiloxane claim 4 , fluorinated or perfluorinated polyacrylate claim 4 , fluorinated or perfluorinated polyolefin claim 4 , fluorinated or perfluorinated polyether claim 4 , fluorinated or perfluorinated polyester claim 4 , and combinations thereof.6. (canceled)7. The composition of claim 1 , wherein at least one of said components (a) and (b) is inorganic; and/or wherein said photoactivatable composition comprises at least one 1 claim 1 ,3-diamine compound that is substituted on at least one nitrogen atom by at ...

Polysiloxane Composition And Cured Product Thereof

The present invention relates to a polysiloxane composition which contains 1. A polysiloxane composition comprising:(A) at least one type of organopolysiloxane that contains at least two unsaturated aliphatic hydrocarbon groups in the molecule,(B) at least one type of organohydrogenpolysiloxane that contains at least two silicon-bonded hydrogen atoms in the molecule,(C) a hydrosilylation reaction catalyst, and(D) inorganic particles which have a major axis to minor axis ratio of 1 to 1.5 and in which the proportion of particles having a diameter of 50 μm or greater is 5 wt. % or less of the total quantity of particles,whereina weight fraction of the unsaturated aliphatic hydrocarbon groups in the organopolysiloxane (A) is from 0.5 to 10 wt. %,a compounding ratio of the inorganic particles (D) in the polysiloxane composition is from 55 to 85 vol. %,a value of [the weight fraction of the unsaturated aliphatic hydrocarbon groups in the organopolysiloxane (A)]×[the weight fraction of the silicon-bonded hydrogen atoms in the organohydrogenpolysiloxane (B)] is from 0.04 to 8, anda viscosity of the polysiloxane composition at 25° C. is 500 Pa·s or less.2. The polysiloxane composition according to claim 1 , wherein the viscosity of the organopolysiloxane (A) at 25° C. is from 0.05 to 20 Pa·s.3. The polysiloxane composition according to claim 1 , wherein the weight fraction of the silicon-bonded hydrogen atoms in the organohydrogenpolysiloxane (B) is 0.1 wt. % or greater.4. The polysiloxane composition according to any one of to claim 1 , wherein the viscosity of the organohydrogenpolysiloxane (B) at 25° C. is 0.1 Pa·s or less.5. The polysiloxane composition according to claim 1 , wherein the value of [the weight fraction of the unsaturated aliphatic hydrocarbon groups in the organopolysiloxane (A)]×[the weight fraction of the silicon-bonded hydrogen atoms in the organohydrogenpolysiloxane (B)] is from 0.1 to 7.6. The polysiloxane composition according to claim 1 , wherein ...

POLYMER COMPOSITION HAVING PHOTOALIGNABLE GROUP, LIQUID CRYSTAL ALIGNMENT FILM FORMED OF THE POLYMER COMPOSITION, AND LIQUID CRYSTAL DISPLAY DEVICE HAVING PHASE DIFFERENCE PLATE FORMED OF THE LIQUID CRYSTAL ALIGNMENT FILM

To provide a photoalignable material that can yield a photoalignable film having a high optical uniformity and no alignment defect, and allows photoalignment with exposure in a short period of time. A photoalignable polymer composition containing a specific photoalignable polymer having a silicone group or a fluorine-substituted alkyl group, and a photoalignable group, and a specific non-photoalignable polymer is manufactured, and the photoalignable film is manufactured by applying the polymer composition onto a base material or the like, drying an applied surface thereon, and irradiating the applied surface with light. 1. A photoalignable polymer composition , containing as a first component a polymer having a silicone group or a fluorine-substituted alkyl group , and a photoalignable group , and as a second component a non-photoalignable polymer obtained by polymerizing a monomer containing at least one kind selected from the group of methacrylic acid and methacrylate.2. The photoalignable polymer composition according to claim 1 , wherein the photoalignable group in the first component includes a functional group having a structure that is photodimerized or photoisomerized.5. The photoalignable polymer composition according to claim 1 , wherein the polymer of the first component has a fluorine-substituted alkyl group and the fluorine-substituted alkyl group is represented by general formula (I-5) as described below.{'br': None, 'Formula 3'}{'br': None, 'sup': '3', '—R\u2003\u2003(I-5)'}{'sup': '3', 'wherein Rrepresents an alkyl group having 1 to 20 carbons in which one or more of arbitrary hydrogen is replaced by fluorine.'}6. The photoalignable polymer composition according to claim 1 , wherein the non-photoalignable polymer of the second component is obtained by polymerizing a monomer containing at least one kind selected from the group of methacrylic acid claim 1 , alkyl methacrylate claim 1 , hydroxyalkyl methacrylate including a hydroxyalkyl group having 2 ...

POLYCARBONATE RESIN COMPOSITION, MOLDED ARTICLE AND STRUCTURE MEMBER FOR SOLAR PHOTOVOLTAIC POWER GENERATION

Provided are: a polycarbonate-based resin composition, including: (A) 100 parts by mass of a resin mixture formed of: 30 to 100 mass % of a PC-POS copolymer (A-1) which has constituent units represented by a general formula (I) and a general formula (II), and in which an average repetition number n of organosiloxane constituent units in the general formula (II) is 70 to 500; and 70 to 0 mass % of an aromatic polycarbonate resin (A-2) except the PC-POS copolymer (A-1); (B) 0.01 to 0.15 part by mass of an alkaline (earth) metal salt of an organic sulfonic acid; (C) 0.1 to 1 part by mass of a polytetrafluoroethylene having a fibril-forming ability; and (D) 2 to 15 parts by mass of titanium dioxide particles each having, on an outermost surface thereof, a coating layer formed of a polyol free of a nitrogen atom; a molded article obtained by molding the resin composition; and a structure member for solar photovoltaic power generation formed of the molded article. The polycarbonate-based resin composition, molded article, and structure member for solar photovoltaic power generation each have excellent flame retardancy and excellent tracking resistance without impairing a low-temperature impact characteristic which a PC-POS copolymer has. 2. The polycarbonate-based resin composition according to claim 1 , wherein the resin mixture (A) comprises a polyorganosiloxane block moiety as the constituent unit of the formula (II) in an amount of 2 to 30 mass %.3. The polycarbonate-based resin composition according to claim 1 ,wherein the polyol free of the nitrogen atom comprises at least one kind selected from the group consisting of trimethylolpropane, trimethylolethane, ditrimethylolpropane, trimethylolpropane ethoxylate, and pentaerythritol.4. The polycarbonate-based resin composition according to claim 1 , wherein the alkaline metal salt claim 1 , the alkaline earth metal salt claim 1 , or both claim 1 , of the organosulfonic acid (B) comprises an alkaline metal salt claim 1 , ...

Epoxy resin composition and light emitting apparatus

Disclosed are an epoxy resin composition and a light emitting apparatus. The epoxy resin composition includes a triazine derivative epoxy resin and a silicon-containing alicyclic epoxy resin

RESIN COMPOSITION, AND PRINTED WIRING BOARD, LAMINATED SHEET, AND PREPREG USING SAME

There are provided a resin composition including: (a) a maleimide compound with at least two N-substituted maleimide groups per molecular structure; and (b) a silicone compound with at least one amino group per molecular structure and also provided a prepreg, a laminated plate, and a printed wiring board that are formed by using this resin composition. The multi-layered printed wiring board produced by using the laminated plate produced by laminating and molding the prepreg obtained from the resin composition of the present invention has excellent glass transition temperature, coefficient of thermal expansion, solder heat resistance, and warp characteristics. The multi-layered printed wiring board is useful as a highly integrated printed wiring board for an electronic device. 1. A resin composition comprising: (a) a maleimide compound with at least two N-substituted maleimide groups per molecular structure; and (b) a silicone compound with at least one amino group per molecular structure.2. The resin composition according to further comprising (c) a compound with a phenolic hydroxyl group per molecular structure.3. The resin composition according to further comprising (d) a thermosetting resin.4. The resin composition according to claim 1 , wherein the silicone compound (b) has at least two amino groups per molecular structure.5. The resin composition according to claim 1 , wherein the silicone compound (b) has an amino group at both ends.6. The resin composition according to claim 1 , wherein the silicone compound (b) has an amino group at either end.7. The resin composition according to claim 1 , wherein the silicone compound (b) has an amino group at a side chain.8. The resin composition according to claim 1 , wherein the silicone compound (b) has an amino group at a side chain and at least one end.9. The resin composition according to claim 1 , wherein the compound (c) has an amino group and a phenolic hydroxyl group per molecular structure.10. The resin ...

COMPOSITIONS CONTAINING SULFONIC ACID CATALYSTS AND METHODS FOR THE PREPARATION AND USE OF THE COMPOSITIONS

A composition is capable of curing via condensation reaction. The composition uses a sulfonic acid condensation reaction catalyst. The sulfonic acid condensation reaction catalyst is used to replace conventional tin catalysts. The composition can react to form a gum, gel, or rubber. 1. A composition comprising:(A) a sulfonic acid condensation reaction catalyst, and(B) a base polymer having an average, per molecule, of one or more hydrolyzable substituents, wherein the composition is capable of reacting via a condensation reaction.2. The composition of claim 1 , wherein the sulfonic acid condensation reaction catalyst comprises a mixed alkyl and aryl sulfonic acid.3. The composition of claim 1 , wherein the sulfonic acid condensation reaction catalyst comprises an aliphatically-substituted polyaromatic disulfonic acid.4. The composition of claim 1 , wherein the sulfonic acid condensation reaction catalyst comprises a catalyst selected from the group of a covalently blocked catalyst claim 1 , a hydrophobic sulfonic acid claim 1 , and combinations thereof.5. The composition of claim 1 , further comprising (C) a silane crosslinker having the general formula RSi(R) claim 1 , where each Ris independently a monovalent hydrocarbon group of 1 to 7 carbon atoms; each Ris independently selected from the group of a halogen atom claim 1 , an acetamido group claim 1 , an acyloxy group claim 1 , an alkoxy group claim 1 , an amido group claim 1 , an amino group claim 1 , an aminoxy group claim 1 , a hydroxyl group claim 1 , an oximo group claim 1 , a ketoximo group claim 1 , or a methylacetamido group; and k is 0 claim 1 , 1 claim 1 , 2 claim 1 , or 3.6. The composition of claim 5 , wherein the sulfonic acid condensation reaction catalyst comprises an aliphatically-substituted polyaromatic sulfonic acid catalyst.7. The composition of claim 6 , wherein the aliphatically-substituted polyaromatic sulfonic acid catalyst is further defined as an aliphatically-substituted naphthalene ...

Rubber Composition Based on a Silicone Elastomer and on a PCM, Process for the Preparation Thereof, Flexible Element and Thermal Control/Regulating System Incorporating Same

A crosslinked rubber composition, process for preparing same, and a flexible component based on at least one room-temperature vulcanizing “RTV” silicone elastomer and including at least one phase change material (PCM) is provided. The flexible element includes at least one elastomer layer capable of storing thermal energy and of releasing it which includes the crosslinked rubber composition. Also provided is a thermal control or regulating system incorporating the flexible element. The composition is such that the silicone elastomer has a viscosity measured at 23° C. according to the ISO 3219 standard which is less than or equal to 5000 mPa.s. The silicone elastomer inlcudes two components A and B and is crosslinked by polyaddition or polycondensation, and the composition includes the PCM, which is not encapsulated and is in the micronized state, in an amount of greater than 50 phr (phr: parts by weight per hundred parts per elastomer(s)).

ROOM TEMPERATURE AND HUMIDITY THICKENING THERMO-CONDUCTIVE SILICON GREASE COMPOSITION

Provided is a room temperature and humidity thickening thermo-conductive silicone grease composition with high shape retention characteristics and good workability despite a low viscosity in an initial phase. Essential components of the room temperature and humidity thickening thermo-conductive silicone grease composition of the present invention are: (A) organopolysiloxane with a viscosity of between 0.1 Pa·s and 1,000 Pa·s at 25° C. with both ends being blocked by a hydroxyl group; (B) organopolysiloxane represented by general equation (1) 4. The heat-conductive silicone grease composition of or , further comprising(I) a silane compound having a group bonded to a silicon atom via a carbon atom, selected from the class consisting of amino, epoxy, mercapto, acryloyl and methacryloyl, and a silicon-bonded hydrolysable group and/or a partial hydrolytic condensate thereof in an amount of 0.01 to 30 parts by weight per 100 parts by weight of components (A) and (B) combined.5. The heat-conductive silicone grease composition of or wherein the silica fine powder as component (F) is surface-treated fumed silica.6. The heat-conductive silicone grease composition of or wherein the thickening catalyst as component (D) is a silane or siloxane containing a guanidyl group. This invention relates to a room temperature and moisture thickening heat-conductive silicone grease composition which is easy to coat and good in shape retention and thus very efficient to work.Currently, an ever increasing need for careful management of energy exists in the electric/electronic, transportation and other fields. For more precise energy control, the system is equipped with more than ever electronic components or parts. In the transportation field, for example, a transition takes place from gasoline vehicles to hybrid vehicles, plug-in hybrid vehicles, and electric vehicles. These hybrid and electric vehicles must be loaded with motors, inverters, batteries, and other electronic components or ...

MICROPATTERNED SILICONE OXYGENATING DRESSING FOR CHRONIC WOUNDS

A wound dressing system having an oxygen-permeable membrane having a first surface and a second surface with oxygen-permeable pillars extending from the second surface is described. 1. A wound dressing system , comprising:a membrane comprised of an oxygen-permeable material, the membrane having a first surface and a second surface with oxygen-permeable pillars extending from the second surface; and interstitial spaces defined between the pillars;the pillars have sidewalls and end surfaces that are oxygen permeable and through which oxygen can diffuse three-dimensionally between and around the pillars;wherein the membrane is configured to be exposed to oxygen such that oxygen can diffuse from the first surface through the oxygen-permeable material toward and through the pillars; and,wherein, in use, the pillars are placed adjacent to the wound and are configured to allow direct delivery of the oxygen into cells of the wound.2. The wound dressing system of claim 1 , further including an oxygen delivery conduit within the membrane that allows oxygen to diffuse through the membrane and the pillars.3. The wound dressing system of claim 2 , wherein the oxygen delivery conduit comprises a porous conduit that extends through the membrane.4. The wound dressing system of claim 1 , further including an oxygen delivery system operatively connected to the membrane.5. The wound dressing system of claim 4 , wherein the oxygen delivery system comprises a supply of an oxygen-containing gas.6. The wound dressing system of claim 5 , wherein the supply of oxygen-containing gas comprises a portable canister.7. The wound dressing system of claim 4 , further includes a tubing that operatively connect the oxygen delivery system to the membrane.8. The wound dressing system of claim 1 , further including a covering on the first side of the membrane.9. The wound dressing system of claim 1 , wherein the oxygen-permeable material comprises an organosilicon polymer.10. The wound dressing system ...

MODIFIED FILLER PARTICLES AND SILICONE COMPOSITIONS COMPRISING THE SAME

Composition of comprising nano metal oxide/hydroxide particles and a polyorganosiloxane having increased refractive index, processes to cure these compositions for making transparent coats, shaped articles by an extrusion or molding process having a refractive index above the refractive index of the polyorganosiloxane. Use of the cured polyorganosiloxane compositions as optical devices, coats, lenses or light guides. 129-. (canceled)32. The composition of claim 31 , wherein L1 is a bond claim 31 , L2 is a C1-C12 alkylene claim 31 , Ris a C1-C22 alkyl claim 31 , and R* is (RO)RSi—.33. The composition of claim 32 , wherein x in R* is 3 claim 32 , and Ris methyl.34. The composition of claim 32 , wherein Ris a C1-C4 alkyl.35. The composition of claim 32 , wherein Ris n-butyl.36. The composition of claim 32 , wherein p is 4 to 9.37. The composition of claim 30 , wherein p is 4 to 9.38. The composition of claim 30 , wherein p is 4 or 9.39. The composition of claim 32 , wherein Ris a C1-C4 alkyl claim 32 , m is 1 claim 32 , and p is 4 to 9.40. The composition of claim 30 , wherein the composition further comprises a crosslinker (C) selected from the group which consists of silanes and siloxanes having reactive groups towards the reactive groups of component (B) claim 30 , whereby the reactive substituents of the crosslinker component (C) are selected from the group which consists of SiH claim 30 , alkenyl claim 30 , alkoxy claim 30 , amino claim 30 , carboxy claim 30 , epoxy claim 30 , and thiol groups.41. The composition of claim 30 , wherein the composition further comprises a crosslinker (C) selected from the group of hydrocarbons without silicon atoms.42. The composition of claim 30 , wherein the metal in the metal oxide or metal hydroxide component (A) is selected from the group of Ti claim 30 , Zr claim 30 , Hf claim 30 , Sn claim 30 , Ce claim 30 , Al claim 30 , As claim 30 , In claim 30 , Zn claim 30 , Ge claim 30 , Sb claim 30 , Cr claim 30 , Cd claim 30 , W claim ...

POLYORGANOSILSESQUIOXANE, HARD COAT FILM, ADHESIVE SHEET, AND LAMINATE

Provided is a polyorganosilsesquioxane capable of forming, when cured, a cured product that offers high surface hardness and good heat resistance, is highly flexible, and has excellent processability. The present invention relates to a polyorganosilsesquioxane including a constitutional unit represented by Formula (1). The polyorganosilsesquioxane includes a constitutional unit represented by Formula (I) and a constitutional unit represented by Formula (II) in a mole ratio of the constitutional unit represented by Formula (I) to the constitutional unit represented by Formula (II) of 5 or more. The polyorganosilsesquioxane has a total proportion of the constitutional unit represented by Formula (1) and a constitutional unit represented by Formula (4) of 55% to 100% by mole based on the total amount (100% by mole) of all siloxane constitutional units. The polyorganosilsesquioxane has a number-average molecular weight of 1000 to 3000 and a molecular-weight dispersity (weight-average molecular weight to number-average molecular weight ratio) of 1.0 to 3.0. 2. The adhesive layer according to claim 1 ,the polyorganosilsesquioxane further comprising {'br': None, 'sup': '2', 'sub': '3/2', '[RSiO]\u2003\u2003(2)'}, 'a constitutional unit represented by Formula (2){'sup': '2', 'wherein Ris selected from a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkyl group, and a substituted or unsubstituted alkenyl group.'}4. The adhesive layer according to claim 2 ,{'sup': '2', 'wherein Ris a substituted or unsubstituted aryl group.'}5. The adhesive layer according to claim 1 ,the curable composition further comprisinga curing catalyst.6. The adhesive layer according to claim 5 ,wherein the curing catalyst comprises a cationic photoinitiator.7. The adhesive layer according to claim 5 ,wherein the curing catalyst comprises a cationic thermal initiator.8. The adhesive ...

CONDENSATION-CROSSLINKING SILICONES WITH IMPROVED RESISTANCE TO TEMPERATURE CHANGE

A silicone formulation that has a) at least one condensation-crosslinkable hydroxy- or alkoxy-terminated polydiorganosiloxane, b) at least one silane crosslinking agent or siloxane crosslinking agent for the hydroxy- or alkoxy-terminated polydiorganosiloxane and c) one or more fillers, where one filler is the main filler, the proportion by weight of which in the silicone formulation is greater than that of any other filler that may be present, and the decomposition temperature of the main filler is above 350° C., with the proviso that the proportion of the main filler in relation to the total weight of the fillers is at least 20% by weight. The silicone formulation is particularly suitable as resilient adhesive or sealant, more particularly for high-temperature applications, e.g. for producing or repairing facades, fireproof joints, windows, insulative glazing, solar installations, vehicles, white or brown goods, heaters, electronic components, or sanitary installations, or for the construction sector. 1. A silicone formulation comprisinga) at least one condensation-crosslinkable hydroxy- or alkoxy-terminated polydiorganosiloxane,b) at least one silane or siloxane crosslinker for the hydroxy- or alkoxy-terminated polydiorganosiloxane, andc) one or more fillers, one filler being the principal filler, which is present in a greater weight fraction than any other filler optionally present in the silicone formulation, and the principal filler having a decomposition temperature of more than 350° C., with the proviso that based on the total weight of the fillers, the fraction of the principal filler is at least 20 wt %.2. The silicone formulation as claimed in claim 1 , wherein the principal filler is selected from dolomites and aluminum oxides claim 1 , the principal filler being optionally surface-modified.3. The silicone formulation as claimed in claim 1 , wherein based on the total weight of the fillers claim 1 , the fraction of the principal filler is 20 to 90 wt %.4. ...

Organic-inorganic composite particles and method for producing same

The present invention provides organic-inorganic composite particles of which the creep deformation is further suppressed; and a method for producing the same. Organic-inorganic composite particles 10 include a compound having a siloxane bond and has a particle diameter d0, and when a load is applied such that an amount of displacement Ds satisfies 0.08d0≤Ds≤0.15d0 and is held for 180 seconds, conditions of the following Formulae (1) and (2) are satisfied: ( D 180− Ds )/ d 0≤1%  Formula(1); and ( D max− Ds )/ d 0≤1%  Formula (2), wherein d0 is an average particle diameter, D180 is an amount of displacement of the particle diameter after 180 seconds of application of the load, and Dmax is the maximum amount of displacement of the particle diameter during the 180 seconds.

Room-temperature-curable silicone composition and electric/electronic apparatus

A room-temperature-curable silicone composition is disclosed. The-room-temperature-curable silicone composition comprises: (A) an organopolysiloxane having alkoxysilyl-containing groups at both molecular terminals; (B) an organopolysiloxane resin; (C) an alkoxysilane; and (D) a condensation-reaction catalyst. The room-temperature-curable silicone composition exhibits good store stability and can form a cured product exhibiting high hardness and good thermal shock stability.

Two-part curable liquid silicone rubber composition

A two-part curable liquid silicone rubber composition is provided in which the first liquid composition and the second liquid composition yield, upon mixing, a curable liquid silicone rubber composition which, when cured, yields a silicone elastomer having an elongation-at-break value of at least 800%. The silicone elastomers of the invention comprise at least one alkenyl group-containing organopolysiloxane having two silicon-bonded alkenyl groups per molecule, at least one diorganohydrogensiloxy-terminated polydiorganosiloxane, at least one organosilicon crosslinker containing at least 3 silicon-bonded hydrogen atoms per molecule, at least one addition reaction catalyst, and at least one filler. Also provided are silicone elastomers having an elongation-at-break value of at least 800% and withstand elongation without breaking. An article for a medical device comprising a cured product of the two-part curable liquid silicone rubber compositions or the silicone elastomers of the invention are also provided.

Silicone Hydrogel Contact Lenses

A method is provided for manufacturing ophthalmically-acceptable, distortion-free silicone hydrogel contact lenses without the use of volatile organic solvents in the manufacturing process. The contact lenses are extract with an extraction liquid comprising an aqueous solution of a non-volatile organic solvent, such as ethyl lactate. 1. A method of manufacturing a silicone hydrogel contact lens comprising:curing a polymerizable composition comprising a siloxane monomer and a hydrophilic monomer to form a cured silicone hydrogel contact lens;hydrating the cured silicone hydrogel contact lens;extracting the hydrated silicone hydrogel contact lens with an extraction liquid comprising an aqueous solution of an organic solvent selected from ethyl lactate, or ethylene carbonate, or propylene carbonate, or propylene glycol, or butanediol, or any combination thereof to make an extracted silicone hydrogel contact lens;removing organic solvent from the extracted silicone hydrogel contact lens to make an ophthalmically-acceptable lens; andpackaging the ophthalmically-acceptable lens.2. The method of claim 1 , wherein the extraction liquid comprises from about 20 wt. % up to about 80 wt. % of the organic solvent.3. The method of claim 1 , wherein the extraction liquid and any other liquid used for processing the cured or hydrated silicone hydrogel contact lens has a flash point of at least 50° C.4. The method of claim 1 , wherein the hydrating comprises contacting the cured silicone hydrogel contact lens with water at a temperature of at least 50° C.5. The method of claim 1 , wherein the polymerizable composition is cured in a mold assembly which is demolded after curing to provide a mold assembly half with the cured silicone hydrogel contact lens adhered thereto claim 1 , and wherein the hydrating step comprises delensing the cured silicone hydrogel contact lens from the mold assembly half by contacting the hydrogel and mold assembly half with an aqueous liquid free of organic ...

COMPLIANT SOLID-STATE IONICALLY CONDUCTIVE COMPOSITE MATERIALS AND METHOD FOR MAKING SAME

Provided herein are ionically conductive solid-state compositions that include ionically conductive inorganic particles in a matrix of an organic material. The resulting composite material has high ionic conductivity and mechanical properties that facilitate processing. In particular embodiments, the ionically conductive solid-state compositions are compliant and may be cast as films. In some embodiments of the present invention, solid-state electrolytes including the ionically conductive solid-state compositions are provided. In some embodiments of the present invention, electrodes including the ionically conductive solid-state compositions are provided. The present invention further includes embodiments that are directed to methods of manufacturing the ionically conductive solid-state compositions and batteries incorporating the ionically conductive solid-state compositions. 180.-. (canceled)81. A solid-state electrode for use in an alkali ion or alkali metal battery , comprising an inorganic phase comprising an ionically conductive inorganic material , an electrochemically active material , and an electronically conductive additive; andan organic phase comprising a first component and a binder, wherein the first component is a non-ionically conductive polymer having a number average molecular weight of between 500 g/mol and 50,000 g/mol and the binder is a non-ion conducting polymer having a number average molecular weight of at least 100 kg/mol.82. The solid-state electrode of claim 81 , wherein the ionically conductive inorganic material constitutes between 15% and 60% by weight of the inorganic phase claim 81 , the electrochemically active material constitutes between 30% and 80% by weight of the inorganic phase claim 81 , and the electronically conductive additive constitutes between 5% and 25% of the inorganic phase.83. The solid-state electrode of claim 81 , wherein the first component constitutes between 50% and 99% by weight of the organic phase claim 81 ...

Resin composition, backing material for ultrasonic vibrator, ultrasonic vibrator, and ultrasonic endoscope

A resin composition of the present invention contains: an epoxy resin (A); a hardener (B); and an ion exchanger (C). At least one of the epoxy resin (A) and the hardener (B) contains a modified silicone (S), and the epoxy resin (A) is at least one type selected from the group consisting of a bisphenol A type epoxy resin, a bisphenol F type epoxy resin, a phenol novolac type epoxy resin, and an epoxy-modified silicone.

METHOD FOR PRODUCING THERMOPLASTIC RESIN COMPOSITION AND THERMOPLASTIC RESIN COMPOSITION

It becomes possible to produce a thermoplastic resin composition having a sea-island structure by a kneading step of kneading a thermoplastic elastomer and/or rubber material having an alkoxysilyl group, in which the alkoxysilyl group is grafted to the thermoplastic elastomer and/or rubber material, and a thermoplastic resin in a melt state in a kneading machine and a dynamic crosslinking step of adding a water component into the kneading machine, forming a silanol group by a hydrolysis reaction of the alkoxysilyl group in the thermoplastic elastomer and/or rubber material having an alkoxysilyl group and the water component in the kneading machine, and subsequently forming a siloxane bond by a condensation reaction between the silanol groups. 1. A thermoplastic resin composition comprising a sea-island structure ,wherein an island structure part of the sea-island structure contains a thermoplastic elastomer and/or rubber material cross-linked by a siloxane bond and a sea structure part of the sea-island structure contains a thermoplastic resin,wherein a gel fraction (in accordance with JIS K 6769: 2004/1SO-15875-2: 2003) of the island structure part is 90% or more, andwherein the blending amount of the thermoplastic resin is 30 to 70 parts by weight relative to 100 parts by weight of the thermoplastic elastomer and rubber material.2. The thermoplastic resin composition according to claim 1 ,wherein the thermoplastic elastomer and/or rubber material is a thermoplastic elastomer in which the main chain and the side chains are formed of saturated bonds, andwherein the thermoplastic resin is a thermoplastic resin in which the main chain and the side chains are formed of saturated bonds.3. The thermoplastic resin composition according to claim 1 ,wherein a viscosity of the thermoplastic elastomer and/or rubber material cross-linked by the siloxane bond is larger than a viscosity of the thermoplastic resin.4. The thermoplastic resin composition according to claim 1 , ...

POLYCARBONATE RESIN COMPOSITION AND MOLDED BODY

Provided is a polycarbonate resin composition, including: 100 parts by mass of (A) a resin mixture including a specific polycarbonate-polyorganosiloxane copolymer (A-1) and a specific polycarbonate-polyorganosiloxane copolymer (A-2), the component (A) having a content of the siloxane unit in the polycarbonate-polyorganosiloxane copolymer (A-1) of 1.0 mass % to 15.0 mass % and having a content of a siloxane unit in the polycarbonate-polyorganosiloxane copolymer (A-2) of 0.1 mass % to 2.8 mass %; and 0.01 to 0.08 part by mass of (B) at least one kind selected from an alkali metal salt of an organic sulfonic acid and an alkali earth metal salt of an organic sulfonic acid. 2. The polycarbonate resin composition according to claim 1 , wherein the component (B) comprises at least one component selected from the group consisting of an alkali metal salt of a perfluoroalkanesulfonic acid and an alkali earth metal salt of a perfluoroalkanesulfonic acid.3. The polycarbonate resin composition according to claim 1 , wherein a molded body of the polycarbonate resin composition having a thickness of 3 mm has a total light transmittance measured based on ISO 13468 of 85% or more.4. The polycarbonate resin composition according to claim 1 , wherein a molded body of the polycarbonate resin composition having a thickness of 2 mm is evaluated as V-0 by a UL94 flame test.5. The polycarbonate resin composition according to claim 1 , wherein the polycarbonate resin composition is free of a bromine-based flame retardant.6. A molded body claim 1 , obtained by a process comprising molding the polycarbonate resin composition of . The present invention relates to a polycarbonate resin composition and a molded body obtained by molding the composition.A polycarbonate resin has self extinguishability, but in electrical and electronic fields such as OA equipment, information and communication equipment, and household electrical appliances, additionally high flame retardancy is required in some ...

Curable organosilicon resin composition

A curable organosilicon resin composition includes; (A) an organopolysiloxane having a resin structure containing 10 to 60 mol % of an R 1 SiO 3/2 unit, 30 to 80 mol % of an (R 2 ) 2 SiO 2/2 unit, and 1 to 30 mol % of an (R 3 ) 3 SiO 1/2 unit. At least a part of the (R 2 ) 2 SiO 2/2 unit is in continuous repeating units with the average number of the repeating units being 3 to 80. The organopolysiloxane has a weight average molecular weight of 5,000 to 50,000; the amount of the hydroxy groups bonded to silicon atoms is 0.001 to 1.0 mol/100 g; and the amount of the alkoxy groups, each having 1 to 10 carbon atoms, bonded to silicon atoms is 1.0 mol/100 g or less. A curable organosilicon resin composition has excellent workability, can give a cured product rapidly, and can make the cured product excellent in mechanical properties, heat resistance, crack resistance, and adhesive property, the surface tackiness being suppressed.

Sealant Composition

The present invention is directed to a sealing composition comprising: (a) a polysiloxane; (b) a reactive polysiloxane comprising at least one reactive functional group; and (c) water; wherein the weight ratio of polysiloxane to reactive polysiloxane is from 2.7:1 to 4:1. Also disclosed are coated substrates and methods of coating a substrate. 1. A sealing composition comprising:(a) a polysiloxane;(b) a reactive polysiloxane comprising at least one reactive functional group; and(c) water;wherein the solids weight ratio of polysiloxane to reactive polysiloxane is from 1.7:1 to 4:1.2. The sealing composition of claim 1 , wherein the polysiloxane comprises at least one silicone resin.3. The sealing composition of claim 1 , wherein the polysiloxane comprises alkoxy groups.4. The sealing composition of claim 1 , wherein the polysiloxane further comprises (meth)acrylate groups claim 1 , polyether groups claim 1 , or combinations thereof.5. The sealing composition of claim 1 , wherein the reactive polysiloxane comprises an amino-functional polysiloxane claim 1 , a hydroxyl-functional polysiloxane claim 1 , or combinations thereof6. The sealing composition of claim 1 , wherein the reactive polysiloxane comprises a polydimethylsiloxane comprising at least one reactive functional group claim 1 , a silsesquioxane comprising at least one reactive functional group claim 1 , or combinations thereof.1. ling composition of claim 1 , further comprising an alkoxy silane.8. The sealing composition of claim 1 , wherein the sealing composition is substantially free of alkoxy silane.9. The sealing composition of claim 1 , further comprising a colorant.10. The sealing composition of claim 1 , wherein sealing composition comprises a sealing composition concentrate having total solids of 30% to 70% claim 1 , based on the total weight of the sealing composition claim 1 , and a viscosity of 4 cST to 1 claim 1 ,200 cST at ambient conditions claim 1 , as measured by an efflux cup according to ...

POLYCARBONATE RESIN, AND POLYCARBONATE RESIN COMPOSITION

Provided is a polycarbonate resin, including, as a dihydric phenol serving as a raw material, a bisphenol A having an isopropenylphenol concentration of 150 ppm by mass or less within 1 hour after granulation and under an ambient temperature condition of from 10° C. to 50° C. 1. A polycarbonate resin , comprising , as a dihydric phenol serving as a raw material , a bisphenol A having an isopropenylphenol concentration of 150 ppm by mass or less within 1 hour after granulation and under an ambient temperature condition of from 10° C. to 50° C.2. The polycarbonate resin according to claim 1 , wherein the polycarbonate resin has a viscosity-average molecular weight of from 9 claim 1 ,000 to 17 claim 1 ,500.3. A polycarbonate resin composition claim 1 , comprising 100 parts by mass of (A) a polycarbonate resin containing 60 mass % or more of the polycarbonate resin of and 100 ppm by mass to 1 claim 1 ,500 ppm by mass of (B) a phosphorus-based antioxidant.4. The polycarbonate resin composition according to claim 3 , wherein (B) the phosphorus-based antioxidant has a pentaerythritol structure.5. The polycarbonate resin composition according to claim 3 , wherein (B) the phosphorus-based antioxidant comprises bis(2 claim 3 ,6-di-tert-butyl-4-methylphenyl)pentaerythritol diphosphite and/or bis(2 claim 3 ,4-dicumylphenyl)pentaerythritol diphosphite.6. The polycarbonate resin composition according to claim 3 , further comprising claim 3 , with respect to 100 parts by mass of (A) the polycarbonate resin claim 3 , 200 ppm by mass to 1 claim 3 ,500 ppm by mass of (C) a polyorganosiloxane having a functional group.7. The polycarbonate resin composition according to claim 6 , wherein the functional group comprises at least one kind selected from the group consisting of an alkoxy group claim 6 , an aryloxy group claim 6 , a polyoxyalkylene group claim 6 , a carboxyl group claim 6 , a silanol group claim 6 , an amino group claim 6 , a mercapto group claim 6 , an epoxy group claim 6 , ...

POLYVINYL BUTYRAL RESIN COMPOSITION, MOLDING AND METHOD OF MANUFACTURING POLYVINYL BUTYRAL RESIN COMPOSITION

A PVB resin composition (R) contains PVB resin (P) and a first resin (Q). A resin molding (U) is formed from a resin (T). The resin (T) includes the PVB resin composition (R) added to a second resin (S). The first resin (Q) may be, for example, PE, PP, PS, ABS, PVC, PET, vinyl acetate, PC, acrylic resin or a copolymer thereof, or a plastic container-recycled material containing one of these resins.

CURABLE RESIN COMPOSITION AND CURED PRODUCT THEREOF, ENCAPSULANT, AND SEMICONDUCTOR DEVICE

Provided is a curable resin composition capable of forming a cured product that has excellent heat resistance and transparency and, in particular, offers excellent barrier properties to a corrosive gas. 117.-. (canceled)19. A cured product of the curable resin composition according to .20. An encapsulant obtained by using the curable resin composition according to .21. A semiconductor device obtained by using the curable resin composition according to . The present invention relates to curable resin compositions; as well as cured products, encapsulants, and semiconductor devices obtained using the curable resin compositions. The present application claims priority to Japanese Patent Application No. 2013-026947 filed in Japan on Feb. 14, 2013, the entire contents of which are incorporated herein by reference.Semiconductor devices require high heat resistance and high breakdown voltage, in which semiconductor elements are covered or encapsulated by materials. These materials generally require such heat resistance as to endure heat at a temperature of about 150° C. or higher. In particular, materials (encapsulants) to cover or encapsulate optical elements such as optical semiconductor elements require excellent physical properties such as transparency and flexibility, in addition to the heat resistance. Such encapsulants currently used typically in backlight units of liquid crystal displays are exemplified by epoxy resin materials and silicone resin materials.Patent Literature (PTL) 1 discloses a synthetic high-molecular compound as a material having high heat resistance and dissipating heat satisfactorily. The synthetic high-molecular compound contains at least one third organosilicon polymer having a molecular weight of from 20000 to 800000. The third organosilicon polymer has been formed by linking at least one first organosilicon polymer with at least one second organosilicon polymer through siloxane bonds. The first organosilicon polymer has a crosslinked siloxane ...

Anti-reflective film

Disclosed herein is an anti-reflective film comprising: a hard coating layer; and a low-refractive layer containing a binder resin and hollow inorganic nanoparticles and solid inorganic nanoparticles which are dispersed in the binder resin, wherein a ratio of an average particle diameter of the solid inorganic nanoparticles to an average particle diameter of the hollow inorganic nanoparticles is 0.26 to 0.55, and wherein at least 70 vol % of the entire solid inorganic nanoparticles are present within a distance corresponding to 50% of an entire thickness of the low-refractive layer from the interface between the hard coating layer and the low-refractive layer, and an anti-reflective film comprising: a hard coating layer containing a binder resin containing a photocurable resin, and organic or inorganic fine particles dispersed in the binder resin; and a low-refractive layer containing a binder resin and hollow inorganic nanoparticles and solid inorganic nanoparticles which are dispersed in the binder resin, wherein a ratio of an average particle diameter of the solid inorganic nanoparticles to an average particle diameter of the hollow inorganic nanoparticles is 0.15 to 0.55, and wherein at least 70 vol % of the entire solid inorganic nanoparticles are present within a distance corresponding to 50% of an entire thickness of the low-refractive layer from the interface between the hard coating layer and the low-refractive layer.

SILANE FUNCTIONAL STABILIZERS FOR EXTENDING LONG-TERM ELECTRICAL POWER CABLE PERFORMANCE

Provided are methods for extending the life of in-service electrical cable having polymeric insulation, comprising injecting a dielectric enhancement fluid composition into the cable, wherein the composition comprises: (a) one or more organoalkoxysilane functional additives (voltage stabilizer-based, hindered amine light stabilizer (HALS)-based, and/or UV absorber-based); and (b) a catalyst suitable to catalyze hydrolysis and condensation of (a), the injected composition providing for rapid initial permeation of (a) into the insulation, and extended retention of subsequent condensation products of (a) in the insulation. Additionally provided are innovative silyl functional ferrocenes (e.g., containing a ferrocene moiety and a silyl function hydrolysable to silanol) having utility as functional voltage stabilizing additives in the methods. 1. A method for extending the useful life of in-service electrical cable , comprising injecting a dielectric enhancement fluid composition into at least one section of an electrical cable having a stranded conductor encased in a polymeric insulation jacket , and having an average operating temperature T , the composition comprising: (i) a voltage stabilizer-based alkoxysilane (e.g., metallocene-based alkoxysilane,', '(ii) a hindered amine light stabilizer (HALS)-based alkoxylsilane (e.g., tetramethyl piperidine-based alkoxysilane), and/or', '(iii) a UV absorber-based alkoxysilane (e.g., benzotriazole-based, triazine-based, nickel chelate-based); and, '(a) at least one organoalkoxysilane functional additive selected from'}(b) at least one catalyst suitable to catalyze hydrolysis and condensation of the at least one functional additive of (a), andwherein the injected composition provides for both initial permeation of the at least one functional additive into the polymeric insulation, and extended retention of subsequent condensation products of the at least one functional additive in the cable insulation.2. The method of claim 1 , ...

IMPROVED FLAME RETARDANT COMPOSITIONS

In an embodiment, a composition comprises a poly(ester-carbonate-siloxane) copolymer; a nanosilica; a plurality of polysiloxane particles; and a fluoropolymer. The nanosilica can be present in an amount of 1 to 5 wt % based on a total weight of the composition. The nanosilica can have a Dparticle size by volume of 5 to 50 nanometers. The nanosilica can have a hydrophobic coating. The plurality of polysiloxane particles can be present in an amount of 1 to 10 wt % based on a total weight of the composition. The plurality of polysiloxane particles can have a Dparticle size by volume of 0.1 to 10 micrometers. The fluoropolymer can be present in an amount of 0.005 to 5 wt % based on a total weight of the composition. 1. A composition comprising:a poly(ester-carbonate-siloxane) copolymer;{'sub': '50', '1 to 5 wt % based on a total weight of the composition of a nanosilica having a Dparticle size by volume of 5 to 50 nanometers; wherein the nanosilica has a hydrophobic coating;'}{'sub': '50', '1 to 10 wt % based on a total weight of the composition of a plurality of polysiloxane particles having a Dparticle size by volume of 0.1 to 10 micrometers; and'}0.005 to 5 wt % based on a total weight of the composition of a fluoropolymer.2. The composition of claim 1 , wherein the composition passes one or more ofa ULV0 rating at a thickness of 0.8 mm, or 0.6 mm, or 0.4 mm;{'sup': 2', '2, 'a 2 minute integrated heat release rate of less than or equal to 55 kW-min/mand a peak heat release rate of less than 55 kW/min accordance with the OSU 55/55 test;'}a peak heat release rate of less than 170 watts per gram as determined in accordance with ASTM D7309-13, method A at a temperature ramp of 1° C./s; or{'sup': 2', '2, 'a smoke density after 4 minutes of less than 150 kW/mand an integral of the smoke density as a function of time up to 4 minutes of less than 300 kW/mdetermined in accordance with ISO 5659-2 using on a 3 mm thick plaque.'}3. The composition of claim 1 , wherein the ...

Curable compositon

Provided is a curable composition and its use. The curable composition may exhibit excellent processibility and workability. The curable composition has excellent light extraction efficiency, crack resistance, hardness, thermal and shock resistance and an adhesive property after curing. The curable composition may provide a cured product exhibiting stable durability and reliability under severe conditions for a long time and having no whitening and surface stickiness.

METHOD FOR ABSORBING LIQUIDS INTO SILICONE-CONTAINING POLYMERS

The invention relates to a method for absorbing liquids (P) containing compounds (V) selected from water and alkanols, the oxygen content of which in weight percentage is at least 27%, said content being present in the loan of hydroxy groups or hydroxy and ether groups, into a solid silicone-containing polymer (P) which contains at least one siloxane unit of the general formula I (R(X)SiOand no units or at least one unit of the general formula II (RSiO, in which R, R, x, a, b, and c have the meanings described in claim wherein the liquids (P) are brought into contact with the solid silicone-containing polymer (P). 1. A method for absorbing liquids (L) comprising: [{'br': None, 'sup': '1', 'sub': b', 'c', '[4−(b+c)]/2, 'R(X)SiO\u2003\u2003(I).'}, {'br': None, 'sup': '2', 'sub': a', '(4−a)/2, 'RSiO\u2003\u2003(II),'}], 'contacting the liquids (L) with solid, silicone-containing polymers (P), wherein the solid, silicone-containing polymers (P) contain at least one siloxane unit of general formula I and optionally at least one unit of general formula II'}in which{'sup': 1', '2', 'x', '3, 'sub': 2', 'd, 'Rand Rare independently hydrogen or an unbranched, branched or cyclic saturated or unsaturated alkyl group with 1 to 20 C atoms or aryl group or aralkyl group, wherein individual non-adjacent methylene units may be replaced by —O—, —CO—. —COO—, —OCO— or —OCOO—, —S— or NRgroups or by an oxyalkylene group of general formula (—O—CH—CHR—),'}{'sup': '3', 'Ris hydrogen or alkyl.'}{'sup': 'x', 'sub': 1', '10, 'Ris hydrogen or a C-Chydrocarbon residue that is unsubstituted or substituted with substituents selected from —CN and halogen,'} {'br': None, 'sup': 4', '5', '6, 'sub': 2', 'e, '—Y—NR—(CH)—CRRCOOM,'}, 'X is a residue bearing at least one amino acid unit and linked to the silicon atom through a carbon atom, having the general formula'}{'sup': 10', '+, 'sub': '4', 'M is hydrogen, metal, or an ammonium residue NR.'}{'sup': '10', 'sub': 1', '12, 'Ris independently hydrogen or ...

Production process for silicone polymer

A process of producing a silicone polymer includes hydrolyzing/condensating one or more compound in the presence of a base, thereby producing a silicone polymer that has an organic acid content of 0.0001 to 0.03 parts by weight with respect to 100 parts by weight of the silicone polymer. The process for producing a silicone polymer makes it possible to inhibit an increase in the molecular weight of a silicone polymer during high-temperature concentration in the steps of producing a silicone polymer.

AEROGEL

The present invention pertains to an aerogel having a thermal conductivity of 0.03 W/m·K or less and a compressive elasticity modulus of 2 MPa or less at 25° C. under atmospheric pressure. 13-. (canceled)4. An aerogel wherein a ratio Q+T:D of a signal area derived from Q and T to a signal area derived from D is from 1:0.01 to 1:0.5 when in a solid Si-NMR spectrum as measured by using DD/MAS method , silicon-containing bonding units of Q , T , and D are defined below:Q: a silicon-containing bonding unit comprising four oxygen atoms that are bonded to one silicon atom;T: a silicon-containing bonding unit comprising three oxygen atoms and one hydrogen atom or one mono-valent organic group that are bonded to one silicon atom; andD: a silicon-containing bonding unit comprising two oxygen atoms and two hydrogen atoms or two mono-valent organic groups that are bonded to one silicon atom,providing that the organic group is a mono-valent organic group where an atom bonded to a silicon atom is a carbon atom.518-. (canceled)19. The aerogel according to claim 4 , having a thermal conductivity of 0.03 W/m·K or less at 25° C. under atmospheric pressure.20. The aerogel according to claim 4 , having a compressive elasticity modulus of 2 MPa or less at 25° C. under atmospheric pressure.21. The aerogel according to claim 4 , having a recovery rate from deformation of 90% or more.22. The aerogel according to claim 4 , having a maximum compressive deformation rate of 80% or more.26. Heat insulating material comprising the aerogel according to . The present invention relates to an aerogel having excellent thermal insulation and productivity.Silica aerogel is known as a material having small thermal conductivity and thermal insulation. Silica aerogel is useful as a functional material having excellent functionalities (e.g., thermal insulation), unique optical properties, and unique electric properties and is, for example, used among others as an electronic substrate material that ...

Organopolysiloxane emulsion composition and resin composition

(In formula (2), EO represents an oxyethylene group; AO represents a linear or branched oxyalkylene group having 3-10 carbon atoms; R1 represents an alkyl group, a hydrogen atom, a carboxy group, an acyl group or a phenyl group; r represents a number of 0-10; s represents a number of 1-100, t represents a number of 0-150; and (s+t) represents a number of 15 or more.)

Compositions and Methods for Injectable Composition for an Accommodating Intraocular Lens

The present disclosure relates to injectable compositions and methods of making injectable compositions of moisture curing siloxane polymers for forming accommodating intraocular lenses. In certain embodiments, the moisture curing siloxane polymers are comprised of an organosilicon compound and a hydrolytically sensitive siloxane moiety and have a specific gravity of greater than about 0.95, a number average molecular weight (M) greater than about 5,000 or about 20,000 and a weight average molecular weight (M) greater than about 20,000 or about 40,000. The disclosure includes accommodating intraocular lenses formed from moisture curing siloxane polymers and having a modulus of elasticity of less than about 6 kPa, less than 20% post-cure extractables, refractive index ranging from 1.4 to 1.5 and dioptric range of accommodation of 0D to 10D. 1. An injectable composition for forming an accommodating intraocular lens in situ in a capsule , comprisingan organosilicon compound anda hydrolytically sensitive siloxane moiety{'sub': n', 'w, 'wherein the injectable composition has a specific gravity greater than about 0.95, a number average molecular weight (M) greater than about 5,000, a weight average molecular weight (M) greater than about 20,000 and is capable of being substantially cured in situ upon contact with moisture.'}2. The injectable composition of claim 1 , wherein the organosilicon compound comprises linear polysiloxane polymer chains claim 1 , linear poly siloxane copolymer chains claim 1 , branched polysiloxane polymer chains claim 1 , or combinations thereof.3. The injectable composition of claim 1 , wherein the injectable composition has a specific gravity in the range of 1 to 1.04.4. The injectable composition of claim 1 , wherein the hydrolytically sensitive siloxane moiety comprises one or more of silane ether groups and/or one of more groups of silane ester groups.5. The injectable composition of claim 1 , wherein the number average molecular weight (M) ...

CURED PRODUCT OF RESIN COMPOSITION, LAMINATE, AND RESIN COMPOSITION

A cured product of a resin composition according to the present invention includes at least silsesquioxane. When the average thermal expansion coefficient of the cured product at 30 to 200° C. is expressed as α1 [K], at least one of requirements α1/α2≥10 and (α1−α2)×10≥0.4 is satisfied, where a reference value α2 is 350×10[K] or less. In the cured product, an absorbance derived from a siloxane bond, an absorbance derived from a hydrocarbon group, and an absorbance derived from a hydroxy group are respectively expressed as Ia, Ib, and Ic, the absorbances being determined by attenuated total reflection using a Fourier transform infrared spectrophotometer. In this case, requirements 0.09≤Ia/Ib≤3.0 and 0.04≤Ic/Ib≤1.0 are satisfied. 1. A cured product of a resin composition , the cured product comprising at least silsesquioxane , wherein{'sup': −1', '2', '8', '−6', '−1, 'when the average thermal expansion coefficient of the cured product at 30 to 200° C. is expressed as α1 [K], at least one of requirements α1/α2≥10 and (α1−α2)×10≥0.4 is satisfied, where a reference value α2 is 350×10[K] or less, and'}requirements 0.09≤Ia/Ib≤3.0 and 0.04≤Ic/Ib≤1.0 are satisfied when an absorbance derived from a siloxane bond in which two silicon atoms are bonded to one oxygen atom, an absorbance derived from a hydrocarbon group, and an absorbance derived from a hydroxy group are respectively expressed as Ia, Ib, and Ic, the absorbances being determined by attenuated total reflection using a Fourier transform infrared spectrophotometer.2. The cured product according to claim 1 , wherein a requirement 0.06≤Ic/Ib≤0.08 or 0.09≤Ic/Ib≤0.10 is further satisfied.3. The cured product according to claim 1 , wherein the silsesquioxane is a polymer of silsesquioxane having an oxetanyl group.4. The cured product according to claim 1 , wherein a relationship Ia/Id≥45 is further satisfied when an absorbance derived from an oxetanyl group and determined by attenuated total reflection using Fourier ...

Curable composition

Provided is a curable composition and its use. The curable composition may exhibit excellent processibility and workability. The curable composition has excellent light extraction efficiency, crack resistance, hardness, thermal and shock resistance and an adhesive property after curing. The curable composition may provide a cured product exhibiting stable durability and reliability under severe conditions in a long time and having no whitening and surface stickiness.

Mesh Size Control of Lubrication in Gemini Hydrogels

A device comprises a surface that is a hydrogel having a targeted mesh size that permits a low-speed friction coefficient near or lower that that typically reported for cartilage of 0.01 to 0.02, a transition. The device can be a contact lens to sit on the cornea where, during a blink, eyelid slides past the eye surface at about 100 mm s. The hydrodynamic lubrication of the hydrogel of the device separates the contact lens surface from the surfaces of the tarsal conjunctiva and marginal conjunctiva of the eyelid. Other devices that can comprise the hydrogel of a targeted mesh size are those that can contact cartilage of articulating joints. 121-. (canceled)22. A soft contact lens , comprising a lens body of a silicone hydrogel material and a coating of a non-silicone hydrogel thereon , wherein the silicone hydrogel material comprises first repeating units of at least one hydrophilic vinylic monomer and second repeating units of at least one silicone-containing vinylic monomer , a silicone-containing vinylic macromer , or a combination thereof , wherein the coating has a thickness of at least 20 nm , wherein the soft contact lens has a surface mesh size of 4.5 nm to 10.6 nm.23. The soft contact lens according to claim 22 , wherein the coating has a thickness of 0.1 μm to 20 μm.24. The soft contact lens according to claim 22 , wherein the coating has a thickness of 0.25 μm to 15 μm.25. The soft contact lens according to claim 22 , wherein the soft contact lens has a surface mesh size of 4.5 nm to 10.6 nm.26. The soft contact lens according to claim 22 , wherein the soft contact lens has a surface mesh size of 6.0 nm to 10.6 nm.27. The soft contact lens according to claim 22 , wherein the soft contact lens has: an elastic modulus of from about 0.1 MPa to 1.8 MPa; a water content of from about 10% to 80% by weight when fully hydrated; a water-break-up time of at least about 10 seconds; a water contact angle of about 100 degrees or less; or any combination thereof.28. ...

COMPOSITION FOR WINDOW FILM, FLEXIBLE WINDOW FILM FORMED THEREFROM, AND FLEXIBLE DISPLAY DEVICE COMPRISING SAME

A composition for a window film including a first silicon resin including a compound represented by Formula 1; a second silicon resin including a crosslinkable functional group and at least one of a Q unit and a bridge unit; a crosslinking agent; and an initiator, a flexible window film formed therefrom, and a flexible display device including the same are disclosed. 1. A composition for a window film comprising:a first silicon resin comprising a compound represented by following Formula 1;a second silicon resin comprising a crosslinkable functional group and at least one of a Q unit and a bridge unit;a crosslinking agent; and {'br': None, 'sup': 1', '2', '3', '4', '5', '6, 'sub': 3/2', 'x', '2/2', 'y', '1/2', 'z, '(RSiO)(RRSiO)(RRRSiO)\u2003\u2003'}, 'an initiator,'}(wherein in Formula 1,{'sup': '1', 'Ris an epoxy group, or an epoxy-group containing functional group,'}{'sup': 2', '3, 'sub': 1', '20', '5', '20, 'Rand Rare each independently hydrogen, a crosslinkable functional group, a substituted or non-substituted Cto Calkyl group, or a substituted or non-substituted Cto Ccycloalkyl group,'}{'sup': 4', '5', '6', '4', '5', '6, 'sub': 1', '20', '5', '20', '6', '30, 'R, Rand Rare each independently hydrogen, a crosslinkable functional group, a substituted or non-substituted Cto Calkyl group, a substituted or non-substituted Cto Ccycloalkyl group, or a substituted or non-substituted Cto Caryl group, at least one of R, Rand Ris a crosslinkable functional group,'}0 Подробнее

PHOTOCHROMIC COMPOUND, CURABLE COMPOSITION CONTAINING SAID PHOTOCHROMIC COMPOUND, AND OPTICAL ARTICLE

The invention is a photochromic compound having an indenonaphthopyran skeleton, and the indenonaphthopyran skeleton has an alkenyl group having 10 to 30 carbon atoms, and an oligomer chain group A having 3 or more recurring units selected from a polyalkylene oxide oligomer chain group, a polyester oligomer chain group, a polysiloxane chain group and a polyester polyether oligomer chain group. The invention can provide a photochromic compound capable of expressing excellent photochromic characteristics in various cured products and capable of preventing cured products from becoming cloudy. 1. A photochromic compound having an indenonaphthopyran moiety , in which the indenonaphthopyran moiety has:an alkenyl group having 10 to 30 carbon atoms, andan oligomer chain group A having 3 or more recurring units selected from a polyalkylene oxide oligomer chain group, a polyester oligomer chain group, a polysiloxane chain group and a polyester polyether oligomer chain group.6. The photochromic compound according to claim 2 ,{'sup': 5', '6, 'wherein Rand Rmay together form, along with the 13-positioned carbon atom in the indenonaphthopyran moiety to which they bond, an aliphatic ring having 3 to 20 ring carbon atoms, a condensed polycyclic ring formed by condensation of the aliphatic ring with an aromatic ring or an aromatic hetero ring, a hetero ring having 3 to 20 ring atoms, or a condensed polycyclic ring formed by condensation of the hetero ring with an aromatic ring or an aromatic hetero ring; and these rings may have a substituent;'}the substituent may be the oligomer chain group A, the alkenyl group having 10 to 30 carbon atoms, or a group having an alkenyl group having 10 to 30 carbon atoms at the terminal thereof.7. The photochromic compound according to claim 1 , having a group to form an aliphatic hydrocarbon ring along with the 13-position carbon atom of the indenonaphthopyran moiety claim 1 , wherein the group to form an aliphatic hydrocarbon ring is a ring ...

Compliant solid-state ionically conductive composite electrolytes and materials

Provided herein are ionically conductive solid-state compositions that include ionically conductive inorganic particles in a matrix of an organic material. The resulting composite material has high ionic conductivity and mechanical properties that facilitate processing. In particular embodiments, the ionically conductive solid-state compositions are compliant and may be cast as films. In some embodiments of the present invention, solid-state electrolytes including the ionically conductive solid-state compositions are provided. In some embodiments of the present invention, electrodes including the ionically conductive solid-state compositions are provided. The present invention further includes embodiments that are directed to methods of manufacturing the ionically conductive solid-state compositions and batteries incorporating the ionically conductive solid-state compositions.

RELEASE AGENT FOR TIRE BLADDER, TIRE BLADDER, AND PNEUMATIC TIRE

A release agent for being coated onto a tire bladder made of a zinc-oxide-incorporated butyl rubber during pneumatic-tire molding, the release agent containing (A) organopolysiloxane, which contains a carboxy group indicated by the general formula (1) below 2. A release agent for application to a tire bladder made of zinc oxide-containing butyl rubber when molding pneumatic tires , which release agent is an aqueous emulsion composition comprising:{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, '(A) 100 parts by weight of the organopolysiloxane of general formula (1) in ,'}(B) from 1 to 30 parts by weight of a surfactant, and(C) from 30 to 10,000 parts by weight of water.3. The release agent for a tire bladder of or , wherein the carboxyl group-containing organopolysiloxane of general formula (1) in component (A) includes: (A-1) a carboxyl group-containing organopolysiloxane wherein n is an integer of 3 or more and less than 150 , and (A-2) a carboxyl group-containing organopolysiloxane wherein n is an integer of 150 or more and not more than 2 ,000.4. The release agent for a tire bladder of claim 3 , wherein the blending ratio of components (A-1) and (A-2) claim 3 , expressed by weight claim 3 , is from 95:5 to 10:90.5. A method of producing a tire bladder for molding pneumatic tires claim 1 , comprising the step of applying the release agent of the composition of to a tire bladder surface made of zinc oxide-containing butyl rubber and subsequently heating at a temperature of between 80 and 250° C.6. A pneumatic tire molded using the tire bladder obtained by the method of . The present invention relates to a release agent which is applied to the surface of a tire bladder made of zinc oxide-containing butyl rubber that is used for molding pneumatic tires, the tire bladder coated with this release agent, and a pneumatic tire molded using this tire bladder.Tire molding is typically carried out by setting an uncured (green) tire in a mold and then inserting a butyl ...

Room-temperature-curable silicone rubber composition, the use thereof, and method for repairing electronic device

A room-temperature-curable silicone rubber composition which exhibits good adhesion to a substrate contacted during curing and which forms a silicone rubber cured product that can be efficiently peeled is disclosed. The room-temperature-curable silicone rubber composition comprises: (A) an organopolysiloxane having in each molecule at least two specified alkoxysilyl-containing groups on silicon atoms in the molecular chain, (B) a diorganodialkoxysilane or partially hydrolyzed condensate thereof, and (C) a condensation-reaction catalyst.

CURABLE SILICONE-BASED COMPOSITIONS AND APPLICATIONS THEREOF

A curable composition comprising a polymer A, a polymer B, and one or more fillers, wherein the polymer A includes organic molecules or siloxane molecules comprising two or more epoxy functional groups, and the polymer B includes an organic amine or a hybrid silicone amine. 2. The curable silicone composition of claim 1 , wherein the one or more amine functional groups of polymer B is situated in the terminal positions claim 1 , pendant position claim 1 , or both in the terminal position and pendant position.3. The curable silicone composition of claim 1 , wherein the polymer A is present in a range from about 5% to about 60% by weight based on the total weight of the composition.4. The curable silicone composition of claim 1 , wherein the polymer B is present in a range from about 5% to about 30% by weight based on the total weight of the composition.5. The curable silicone composition of claim 1 , wherein the composition comprises one or more fillers selected from the group consisting of alumina claim 1 , silicon claim 1 , magnesia claim 1 , ceria claim 1 , hafnia claim 1 , lanthanum oxide claim 1 , neodymium oxide claim 1 , samaria claim 1 , praseodymium oxide claim 1 , thoria claim 1 , urania claim 1 , yttria claim 1 , zinc oxide claim 1 , zirconia claim 1 , silicon aluminum oxynitride claim 1 , borosilicate glasses claim 1 , barium titanate claim 1 , silicon carbide claim 1 , silica claim 1 , boron carbide claim 1 , titanium carbide claim 1 , zirconium carbide claim 1 , boron nitride claim 1 , silicon nitride claim 1 , aluminum nitride claim 1 , titanium nitride claim 1 , zirconium nitride claim 1 , zirconium boride claim 1 , titanium diboride claim 1 , aluminum dodecaboride claim 1 , barytes claim 1 , barium sulfate claim 1 , asbestos claim 1 , barite claim 1 , diatomite claim 1 , feldspar claim 1 , gypsum claim 1 , hormite claim 1 , kaolin claim 1 , mica claim 1 , nepheline syenite claim 1 , perlite claim 1 , phyrophyllite claim 1 , smectite claim 1 , talc ...

METHOD FOR PRODUCING THERMOPLASTIC RESIN COMPOSITION AND THERMOPLASTIC RESIN COMPOSITION

It becomes possible to produce a thermoplastic resin composition having a sea-island structure by a kneading step of kneading a thermoplastic elastomer and/or rubber material having an alkoxysilyl group, in which the alkoxysilyl group is grafted to the thermoplastic elastomer and/or rubber material, and a thermoplastic resin in a melt state in a kneading machine and a dynamic crosslinking step of adding a water component into the kneading machine, forming a silanol group by a hydrolysis reaction of the alkoxysilyl group in the thermoplastic elastomer and/or rubber material having an alkoxysilyl group and the water component in the kneading machine, and subsequently forming a siloxane bond by a condensation reaction between the silanol groups. 1. A method for producing a thermoplastic resin composition , comprising:a kneading step of kneading a thermoplastic elastomer and/or rubber material having an alkoxysilyl group, in which the alkoxysilyl group is grafted to the thermoplastic elastomer and/or rubber material, and a thermoplastic resin in a melt state in a kneading machine; anda dynamic crosslinking step of adding a water component into the kneading machine, forming a silanol group by a hydrolysis reaction of the alkoxysilyl group in the thermoplastic elastomer and/or rubber material having an alkoxysilyl group and the water component in the kneading machine, and subsequently forming a siloxane bond by a condensation reaction between the silanol groups,wherein the thermoplastic resin composition obtained by the dynamic crosslinking step has a sea-island structure.2. The method for producing a thermoplastic resin composition according to claim 1 , wherein in the dynamically crosslinking step claim 1 ,when the alkoxysilyl group of the thermoplastic elastomer and/or rubber material having an alkoxysilyl group forms the siloxane bond passing through the silanol group,a viscosity of the thermoplastic elastomer and/or rubber material having an alkoxysilyl group becomes ...

NANOCOMPOSITE SILICON OXYGEN CARBON MATERIALS AND USES

Nanocomposite silicon and carbon compositions. These compositions can be made from polymer derived ceramics, and in particular, polysilocarb precursors. The nanocomposite can have non-voids or be nano-void free and can form larger macro-structures and macro-composite structures. The nanocomposite can contain free carbon domains in an amorphous SiOC matrix. 142-. (canceled)43. A nanocomposite material comprising: a first composition comprising a free carbon domain and a second composition comprising a plurality of silicon based moieties; and wherein the first and second compositions are different compositions.44. The nanocomposite material of claim 43 , wherein the free carbon domain is selected from the group consisting of spcarbon claim 43 , aromatic structures having 6 or more carbons claim 43 , bent ring aromatic structures claim 43 , conjugated aliphatic carbons claim 43 , conjugated aliphatic carbons having from 3 to 10 carbons claim 43 , conjugated aliphatic carbons having from 10 to 20 carbons claim 43 , and alkanes.45. The nanocomposite material of claim 43 , wherein the free carbon domain is selected from the group consisting of turbostratic claim 43 , amorphous claim 43 , graphenic claim 43 , and graphitic.46. The nanocomposite material of claim 43 , wherein at least one of the moieties is selected from the group consisting of Si(CH)O claim 43 , SiCO claim 43 , SiC claim 43 , Si(CH)O claim 43 , SiCO claim 43 , Si(CH)(OH)O claim 43 , SiCOSiO claim 43 , esters claim 43 , ketones claim 43 , C—O—C claim 43 , C—O—Si claim 43 , Si(CH)O claim 43 , Si—C—C—Si claim 43 , Si(CH)O claim 43 , and Si(CH)O.47. The nanocomposite material of claim 44 , wherein at least one of the moieties is selected from the group consisting of Si(CH)O claim 44 , SiCO claim 44 , SiC claim 44 , Si(CH)O claim 44 , SiCO claim 44 , Si(CH) (OH)O claim 44 , SiCOSiO claim 44 , esters claim 44 , ketones claim 44 , C—O—C claim 44 , C—O—Si claim 44 , Si(CH)O claim 44 , Si—C—C—Si claim 44 , Si(CH)O ...

IONOMERIC SILICONE THERMOPLASTIC ELASTOMERS

This invention relates to thermoplastic elastomers comprising at least one silicone ionomer. These thermoplastic elastomers may be reprocessed and/or recycled. 1. A thermoplastic elastomer comprising at least one silicone ionomer having an average Formula (1) (XRSiO)(XRSiO)(XRSiO)(SiO)where each R is an independently selected monovalent alkyl group or aryl group , each X is independently selected from a monovalent alkyl group , aryl group and a carboxy functional group having a Formula (2) -G-COOZ , where G is a divalent spacer group having at least 2 spacing atoms , each Z is independently selected from hydrogen or a cation independently selected from alkali metal cations , alkali earth metal cations , transition metal cations , and metal cations , v is 0 to 3 , w is 0 to 2 , y is 0 to 1 , 0≦a≦0.9; 0≦b<1; 0≦c<0.9 , 0≦d<0.3 and a+b+c+d=1 , provided that on average there is at least 0.002 mole carboxy functional groups per silicon atom and at least 10 mole percent of the Z groups of the carboxy functional group are an independently selected cation.2. The thermoplastic elastomer of where at least 50 mole percent of the Z groups of the carboxy functional group are an independently selected cation.3. The thermoplastic elastomer of where at least 75 mole percent of the Z groups of the carboxy functional group are an independently selected cation.4. The thermoplastic elastomer of where 100 mole percent of the Z groups of the carboxy functional group are an independently selected cation.5. The thermoplastic elastomer of any of to where the cation is selected from Li claim 1 , Na claim 1 , K claim 1 , Cs claim 1 , Mg claim 1 , Ca claim 1 , Ba claim 1 , Zn claim 1 , Cu claim 1 , Ni claim 1 , Ga claim 1 , Al claim 1 , Mn claim 1 , and Cr.6. The thermoplastic elastomer of any of to where the cation is selected from Li claim 1 , Na claim 1 , K claim 1 , Zn claim 1 , Ni claim 1 , Al claim 1 , Mn claim 1 , Mg.7. The thermoplastic elastomer of any of to where on average there are ...

System and method for separating an aqueous liquid into at least two cavities

The present disclosure relates to a method for separating an aqueous liquid comprising biological material into at least two cavities, the use of a polysiloxane having at least one hydroxy group in such a method, as well as a system for separating an aqueous liquid into at least two cavities.

Manufacturing Method For High-Purity Glycerol Derivative-Modified Silicone

The present invention relates to a manufacturing method for a liquid high-purity glycerin derivative-modified silicone, the method comprising: a step of adding, to a mixture containing a glycerin derivative-modified silicone and impurities, an organic wax having affinity with the impurities and having a higher melting point than the glycerin derivative-modified silicone, melting and mixing while heating, and introducing the impurities into the melted organic wax; a step of obtaining a solidified product of the organic wax by cooling the organic wax; and a step of performing solid-liquid phase separation on the glycerin derivative-modified silicone and the solidified product of the organic wax. With the present invention, it is possible to provide a useful method for stably producing a high-purity glycerin derivative-modified silicone on a commercial scale.

POLYSILOXANE RESIN COMPOSITION

A composition which provides a coating film having excellent foul releasing property is disclosed. The composition comprises, based on the solid contents of the composition: (A) 20 to 80 weight % of a resin which has a polydialkylsiloxane unit and an epoxy resin unit within its structure; (B) 0.1 to 5 weight % of an amino silane; (C) 0.5 to 5 weight % of a hydrophilic additive; and (D) 0.1 to 5 weight % of a catalyst. A coating, e.g. a coating film, formed from the composition generally has an amphiphilic surface. Thus, the composition is suitable for coatings which prevent both hydrophobic and hydrophilic fouling. 1. A composition comprising:(A) 20 to 80 weight % of a resin which has a polydialkylsiloxane unit and an epoxy resin unit within its structure;(B) 0.1 to 5 weight % of an amino silane;(C) 0.5 to 5 weight % of a hydrophilic additive; and(D) 0.1 to 5 weight % of a catalyst;each weight % based on the solid contents of the composition.2. The composition of claim 1 , wherein the epoxy resin unit in the resin (A) is an aliphatic epoxy resin.3. The composition of claim 1 , wherein the polydialkylsiloxane unit in the resin (A) comprises a polydimethylsiloxane.4. The composition of claim 1 , wherein the weight ratio of the polydialkylsiloxane unit and the epoxy resin unit within the resin (A) is from 5:1 to 1:5.5. The composition of claim 1 , wherein the hydrophilic additive (C) is selected from the group consisting of a silicone polyether fluid claim 1 , a fluoroalkoxy substituted methyl silicate polymer claim 1 , a hydrophilic silica sol claim 1 , a hydrophilic aluminum sol claim 1 , and combinations thereof.6. A film formed from the composition of .7. The film of claim 6 , wherein the film is formed on an article selected from the group consisting of drums of washing machines claim 6 , internal surfaces of washing machines claim 6 , washing machine tripods claim 6 , kitchen sinks claim 6 , and combinations thereof.8. The composition of claim 1 , further defined ...

Curable Silicone Compositions

The invention relates to curable compositions based on polyorganosiloxanes with special silicon-containing terminal groups, a special capped adhesion promoter, and a curing catalyst. These compositions have improved adhesion properties and excellent storage stability. The invention furthermore relates to the use thereof. 2. The curable composition according to claim 1 , wherein the polyorganosiloxane is a polydiorganosiloxane.3. The curable composition according to claim 1 , wherein the polyorganosiloxane is a polydimethylsiloxane (PDMS).4. The curable composition according to claim 1 , wherein A is a bond claim 1 , —O— or a linear or branched divalent group selected from siloxane-alkylene.5. The curable composition according to claim 1 , wherein A is a bond claim 1 , —O— or a linear or branched divalent group of the formula —(CH)—(Si(Alk)-O—Si(Alk))—(CH) claim 1 , or a derivative thereof claim 1 , with Alk being Calkyl.6. The curable composition according to claim 1 , wherein{'sup': '1', 'each Ris independently selected from an alkyl group having 1 to 10 carbon atoms; an alkenyl group having 2 to 10 carbon atoms; an aryl group having 6 to 10 carbon atoms; an aryloxy group having 6 to 14 carbon atoms; an acyloxy group having 2 to 10 carbon atoms; or amino; and/or'}{'sup': 2', '4', '5', '5', '5, 'sub': '2', 'each Ris independently selected from a group of the formula (2), wherein Rstands for a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms; and Y is selected from a substituted or unsubstituted aromatic group having 6 carbon ring atoms, or —(C(R))—, wherein o is 1 and one of the Rgroups is hydrogen and the second Rgroup is a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms.'}7. The curable composition according to claim 4 , wherein one of the Rgroups is hydrogen and the second Rgroup is a substituted or unsubstituted alkyl group selected from methyl claim 4 , carboxymethyl or an (alkyl) ester thereof.8. The curable composition ...

Anti-soiling agent composition

[Object] To provide an anti-soiling agent compound that can sufficiently prevents adhesion of pitch to a dry part region. [Solution] The present invention provides an anti-soiling agent composition is provided with: a low molecular polysiloxane compound represented by the following formula (1); and a high molecular polysiloxane compound represented by the following formula (2), and characterized in that the number of modified groups per low molecular polysiloxane compound is in a range from 0.1 to 3, the number of modified groups per high molecular polysiloxane compound is in a range from 1.0 to 10, and the number m of repeating polysiloxane units in the low molecular polysiloxane compound and the number n of repeating polysiloxane units in the high molecular polysiloxane compound have the following relationship: 2 m≦n, [in formula (1), substituent R 1 represents a methyl group or a modified group, with the repeating number m being set to an integer from 20 to 200], and [in formula (2), substituent R 2 represents a methyl group or a modified group, with the repeating number n representing an integer].

SILICONE EMULSION COMPOSITION CAPABLE OF BEING FORMED INTO COATING FILM, AND COATING FILM

A silicone emulsion composition capable of being formed into a coating film, which contains: (A) 100 parts by mass of an organopolysiloxane containing, per molecule, at least two groups each capable of binding to a silicon atom, wherein the at least two groups are independently selected from a hydroxyl group and an alkoxy group; (B) 0.1 to 50 parts by mass of a surfactant; (C) 0.01 to 10 parts by mass of at least one substance selected from cellulose and a cellulose derivative; (D) 0.5 to 50 parts by mass of colloidal silica; and (E) 50 to 1,000 parts by mass of water. 1. A film-forming silicon emulsion composition comprising:(A) 100 parts by weight of an organopolysiloxane having at least two groups selected from silicon-bonded hydroxyl groups and alkoxy groups per molecule,(B) from 0.1 to 50 parts by weight of a surfactant,(C) from 0.01 to 10 parts by weight of one or more substance selected from cellulose and cellulose derivatives,(D) from 0.5 to 50 parts by weight of colloidal silica, and(E) from 50 to 1,000 parts by weight of water.2. The film-forming silicone emulsion composition of claim 1 , wherein the cellulose is cellulose nanofibers.3. The film-forming silicone emulsion composition of claim 1 , wherein the cellulose derivative is an alkyl cellulose claim 1 , a hydroxyalkyl alkyl cellulose claim 1 , a carboxy alkyl cellulose claim 1 , a carboxy alkyl cellulose salt claim 1 , or a mixture thereof.4. The film-forming silicone emulsion composition of claim 3 , wherein the alkyl cellulose is methyl cellulose.5. The film-forming silicone emulsion composition of claim 3 , wherein the hydroxyalkyl alkyl cellulose is hydroxypropyl methyl cellulose or hydroxyethyl methyl cellulose.6. The film-forming silicone emulsion composition of claim 3 , wherein the carboxy alkyl cellulose is carboxy methyl cellulose and the carboxy alkyl cellulose salt is carboxy methyl cellulose sodium.7. The film-forming silicone emulsion composition of claim 1 , which contains no organotin ...

Composition for Forming Hard Coating Layer, Method of Preparing Hard Coating Film and Hard Coating Film Prepared by Using the Same

Provided is a composition for forming a hard coating layer, which includes an epoxy siloxane resin, a crosslinking agent including a compound having an alicyclic epoxy group, a thermal initiator including a compound represented by Chemical Formula 2, and a photoinitiator to decrease curls and increase hardness of the hard coating film. 2. The composition for forming a hard coating layer of claim 1 , wherein the epoxy siloxane resin has a weight average molecular weight of 1 claim 1 ,000 to 20 claim 1 ,000.5. The preparation method of a hard coating film of claim 4 , wherein the epoxy siloxane resin has a weight average molecular weight of 1 claim 4 ,000 to 20 claim 4 ,000.7. The preparation method of a hard coating film of claim 4 , wherein the thermally curing is carried out at a temperature of 100 to 200° C. for 5 to 20 minutes.8. The preparation method of a hard coating film of claim 4 , further comprising: pretreating the composition for forming a hard coating layer by heating before the ultraviolet irradiation.9. The preparation method of a hard coating film of claim 8 , wherein the pretreating is carried out at lower temperature than the thermal curing temperature.10. The preparation method of a hard coating film of claim 4 , further comprising:further applying the composition for forming a hard coating layer to a surface of the substrate on which the complexly cured hard coating layer is not formed; andultraviolet-curing the further applied composition for forming a hard coating layer to form a photocured hard coating layer.11. The preparation method of a hard coating film of claim 10 , wherein a thickness ratio of the complexly cured hard coating layer to the photocured hard coating layer is 1.1:1 to 8:1.12. A hard coating film comprising:a substrate; anda complexly cured hard coating layer formed by complexly curing a composition including an epoxy siloxane resin and a crosslinking agent including a compound having an alicyclic epoxy group, on the substrate ...

Sorbent material and method for using the same

Disclosed is a swellable, sorbent material formed of a sol-gel composition having a porous matrix and a sorbent property modifier intermixed with at least a portion of the porous matrix. The sorbent property modifier modifies a sorbent property of the sorbent material when compared to the same sorbent property of the corresponding, unmodified sol-gel composition.

SILICONE-CONTAINING PRESSURE-SENSITIVE ADHESIVE AND PRESSURE-SENSITIVE ADHESIVE PRODUCTS SUCH AS AN ADHESIVE TAPE OR A LABEL, AND PROCESS FOR PRODUCING SAME

An adhesive containing silicone, in the form of an adhesive compound which contains at least a first adhesive component and a second adhesive component containing silicone is provided. The second, silicon-laced adhesive component consists of a non-crosslinked polysiloxane. The kinematic viscosity of the non-crosslinked polysiloxane is at least 100,000 mm/s and at most 10,000,000 mm/s or that the molar mass of the non-crosslinked polysiloxane is less than 10,000 g/mol, and the second, silicone-containing adhesive component is microencapsulated. Alternatively it can be provided that the molar mass of the polysiloxane is at least 80,000 g/mol and at most 500,000 g/mol, or that the kinematic viscosity of the non-crosslinked polysiloxane is less than 100,000 mm/s, and the second, silicone-containing adhesive component is microencapsulated. 1. An adhesive comprising a first adhesive component and a second , silicone-containing adhesive component , wherein the second , silicon-containing adhesive component consists of a non-crosslinked polysiloxane ,{'sup': 2', '2, 'wherein the kinematic viscosity of the non-crosslinked polysiloxane is at least 100,000 mm/s and at most 10,000,000 mm/s or that the molar mass of the non-crosslinked polysiloxane is less than 10,000 g/mol, wherein the second, silicone-containing adhesive component is microencapsulated.'}2. An adhesive comprising a first adhesive component and a second , silicone-containing adhesive component , wherein the second , silicon-containing adhesive component consists of a non-crosslinked polysiloxane ,{'sup': '2', 'wherein the molar mass of the non-crosslinked polysiloxane is at least 80,000 g/mol and at most 500,000 g/mol, or that the kinematic viscosity of the non-crosslinked polysiloxane is less than 100,000 mm/s, wherein the second, silicone-containing adhesive component is microencapsulated.'}3. The adhesive according to claim 1 ,wherein the second, silicone-containing adhesive component consists of a non- ...

ONE-PART ROOM-TEMPERATURE CURABLE COMPOSITIONS ON THE BASIS OF ORGANOSILICON COMPOUNDS AND TITANIUM CURING CATALYSTS

One-part room-temperature curable compositions (RTV-1 compositions) based on organosilicon compounds are less toxic compared to conventional compositions containing organotin compounds and, at the same time, have excellent curing properties, a skin formation time which allows proper handling and tooling, and excellent storage stability. The compositions contain: at least one organosilicon compound containing condensable groups; at least one curing agent having the formula R′Si(OOCR″), wherein R′ is C-Calkyl, and R″ is C-Calkyl; at least one organotitanium compound curing catalyst; and at least one filler. 119.-. (canceled)21. The curable composition of claim 20 , wherein the curable composition is free of organotin compounds.22. The curable composition of claim 20 , wherein curing agent composition (B) is present in an amount of 2.5 wt.-% or more to 6 wt.-% or less based on the total weight of the curable composition.23. The curable composition of claim 20 , wherein curing agent composition (B) is present in an amount of from 4 to 10 parts by weight claim 20 , based on 100 parts by weight of component (A).24. The curable composition of claim 20 , wherein component (C) is present in an amount of from 0.001 to 2 parts by weight claim 20 , based on 100 parts by weight of component (A).25. The curable composition of claim 20 , wherein component (C) is present in an amount of from 0.001 to 0.5 parts by weight claim 20 , based on 100 parts by weight of component (A).26. The curable composition of claim 20 , wherein the curable composition comprises filler(s) (D) in an amount of greater than 0 and up to 300 parts by weight claim 20 , based on 100 parts by weight based of organosilicon compound (A).27. The curable composition of claim 20 , wherein the curable composition comprises filler(s) (D) in an amount of from 5 to 150 parts by weight claim 20 , based on 100 parts by weight of organosilicon compound (A).28. The curable composition of claim 20 , wherein the curable ...

STORAGE-STABLE ONE-PART ROOM-TEMPERATURE CURABLE COMPOSITIONS ON THE BASIS OF ORGANOSILICON COMPOUNDS

One-part room-temperature curable compositions (RTV-1 compositions) based on organosilicon compounds have improved storage stability and excellent physical properties, and contain (A) at least one organosilicon compound containing condensable groups, (B) at least one curing agent comprising a combination of n-propyltriacetoxysilane and methyltriacetoxysilane, and (C) at least one curing catalyst comprising an organotin compound. The curing agent is a combination of n-propyltriacetoxysilane and methyltriacetoxysilane reduces the tendency of the composition to crystallize without impairing the chemical and physical properties of the composition. 112.-. (canceled)13. A one-part room-temperature curable composition , comprising:(A) at least one organosilicon compound containing condensable groups;(B) at least one curing agent comprising a combination of n-propyltriacetoxysilane and methyltriacetoxysilane; and(C) at least one curing catalyst comprising an organotin compound.14. The composition of claim 13 , wherein the curing agent (B) comprises at least 50 wt. % of n-propyltriacetoxysilane based on the total weight of the curing agent.15. The composition of claim 13 , wherein the curing agent (B) further comprises condensates of two or more molecules of n-propyltriacetoxysilane claim 13 , methyltriacetoxysilane or a combination thereof.16. The composition of claim 15 , wherein up to 30% of all Si atoms of the curing agent are contained in the condensates.17. The composition of claim 13 , wherein the curing agent (B) further comprises a compound other than n-propyltriacetoxysilane claim 13 , methyltriacetoxysilane or condensates thereof claim 13 , said compound having the formula (III):{'br': None, 'sub': c', '(4-c), 'sup': '1', 'ZSiR\u2003\u2003(III),'}wherein{'sup': '1', 'Reach is identical or different and is a monovalent, unsubstituted or substituted hydrocarbon radical, wherein one or more carbon atoms of the hydrocarbon radical are optionally replaced with oxygen ...

Self-welding high dielectric silicone rubber composition and self-welding high dielectric tape

Provided are a self-welding high dielectric silicone rubber composition and a self-welding high dielectric tape. The self-welding high dielectric silicone rubber composition comprises: (A) 100 parts by mass of an organopolysiloxane represented by an average composition formula (1) and having, in a molecule, at least two alkenyl groups bonded to silicon atoms, R1nSiO(4-n)/2 (1), (in the formula, R1 represents the same or different, unsubstituted or substituted monovalent hydrocarbon group and n is a positive number of 1.95 to 2.04); (B) 10 to 100 parts by mass of hydrophobic fumed silica having a specific surface area obtained by the BET adsorption method of 50 m2/g or larger; (C) 100 to 300 parts by mass of a conductive complex oxide; (D) 0.1 to 50 parts by mass of a boric acid or a boric acid compound; (E) 1 to 10 parts by mass of a diorganopolysiloxane capped at both molecular terminals with alkoxy groups; and (F) 0.01 to 10 parts by mass of a curing agent comprising an acyl organic peroxide. The self-welding high dielectric silicone rubber composition can be hot-air vulcanized under normal pressure by extrusion molding or roll forming with calender rolls.

COMPOSITION FOR ORGANIC ELECTRONIC ELEMENT ENCAPSULANT, AND ENCAPSULANT FORMED BY USING SAME

A composition for an encapsulant according to one embodiment of the present application comprises 1) a silicone resin, 2) one or more types of moisture absorbent, 3) one or more types of photoinitiator, 4) one or more types of fillers, and 5) a reactive silicone oligomer. 1. A composition for an encapsulant , comprising:1) a silicone resin;2) one or more moisture absorbents;3) one or more photoinitiators;4) one or more fillers; and5) a reactive silicone oligomer.2. The composition of claim 1 , wherein the silicone resin is an organopolysilicone-based resin.4. The composition of claim 1 , wherein a content of the silicone resin is 1 to 80 wt % based on a total weight of the composition for an encapsulant.5. The composition of claim 1 , wherein the moisture absorbent comprises one or more selected from the group consisting of a metal powder claim 1 , a metal oxide claim 1 , an organic metal oxide claim 1 , a metal salt and phosphorus pentoxide (PO).6. The composition of claim 1 , wherein a content of the moisture absorbent is 10 to 90 wt % based on the total weight of the composition for an encapsulant.7. The composition of claim 1 , wherein the filler comprises one or more selected from the group consisting of clay claim 1 , talc claim 1 , silica claim 1 , barium sulfate claim 1 , aluminum hydroxide claim 1 , calcium carbonate claim 1 , magnesium carbonate claim 1 , zeolite claim 1 , zirconia claim 1 , titania claim 1 , and montmorillonite.8. The composition of claim 1 , wherein a content of the filler is more than 0 and 20 wt % or less based on the total weight of the composition for an encapsulant.9. The composition of claim 1 , wherein a content of the photoinitiator is 0.1 to 10 wt % based on the total weight of the composition for an encapsulant.11. The composition of claim 1 , wherein a content of the reactive silicone oligomer is 1 to 40 wt % based on the total weight of the composition for an encapsulant.12. An encapsulant formed by using the composition for ...

NANOCOMPOSITE SILICON OXYGEN CARBON MATERIALS AND USES

Nanocomposite silicon and carbon compositions. These compositions can be made from polymer derived ceramics, and in particular, polysilocarb precursors. The nanocomposite can have non-voids or be nano-void free and can form larger macro-structures and macro-composite structures. The nanocomposite can contain free carbon domains in an amorphous SiOC matrix. 1. A nanocomposite material comprising: a first composition comprising silicon , free carbon and a first moiety and a second composition comprising silicon and a second moiety; and wherein the first and second compositions are different compositions.2. The nanocomposite of claim 1 , wherein the first moiety and the second moiety are the same.3. The nanocomposite of claim 1 , wherein the first moiety and the second moiety are different.4. The nanocomposite of claim 1 , comprising a third composition; and wherein the third composition is different from the first and second compositions.5. The nanocomposite of claim 2 , comprising a third composition; and wherein the third composition is different from the first and second compositions.6. The nanocomposite of claim 3 , comprising a third composition; and wherein the third composition is different from the first and second compositions.7. The nanocomposites of claim 1 , wherein the first composition is a polymer derived ceramic composition and is a bulk phase.8. The nanocomposites of claim 2 , wherein the first composition is a polymer derived ceramic composition and is a bulk phase.9. The nanocomposites of claim 3 , wherein the first composition is a polymer derived ceramic composition and is a bulk phase.10. The nanocomposites of claim 1 , wherein the second composition is a polymer derived ceramic composition and is a bulk phase.11. The nanocomposites of claim 2 , wherein the second composition is a polymer derived ceramic composition and is a bulk phase.12. The nanocomposites of claim 3 , wherein the second composition is a polymer derived ceramic composition and ...

Encapsulating sheet, optical semiconductor device, and producing method thereof

An encapsulating sheet, for encapsulating an optical semiconductor element mounted on a board by a wire-bonding connection, includes an embedding layer for embedding the optical semiconductor element and a wire and a cover layer covering the embedding layer. The embedding layer and the cover layer contain a catalyst containing a transition metal and are prepared from a silicone resin composition that is cured by accelerating a reaction by the catalyst. The ratio of the concentration of the transition metal in the cover layer to that of the transition metal in the embedding layer is 1 or more. The length from an interface between the embedding layer and the cover layer to a portion of the wire that is positioned closest to the cover layer-side is 150 μm or more.

Silicone materials

Silicone material obtained by a reaction between:—at least one organopolysiloxane (A) that has a molar mass of less than 70,000 g/mol, preferably less than 50,000 g/mol, and contains siloxyl units I.1 and I.2; and—at least one organic compound (B) carrying at least two carboxylic acid groups and having no unsaturation. Y a  Z b 1  SiO 4 - ( a + b ) 2 ( I  .1 ) Z c 2  SiO 4 - c 2 ( I  .2 )

RESIN COMPOSITION, RESIN FILM, SEMICONDUCTOR LAMINATE, METHOD FOR MANUFACTURING SEMICONDUCTOR LAMINATE, AND METHOD FOR MANUFACTURING SEMICONDUCTOR DEVICE

The present invention is a resin composition including: (A) an epoxy resin; (B) an epoxy compound shown by the following formula (1) and/or formula (2); (C) a phenolic curing agent; and (D) a curing accelerator, 2. The resin composition according to claim 1 , wherein the component (A) is a silicone-modified epoxy resin.4. The resin composition according to claim 1 , wherein the resin composition exhibits a tensile strength of 6.0 MPa or more after being cured.5. The resin composition according to claim 2 , wherein the resin composition exhibits a tensile strength of 6.0 MPa or more after being cured.6. The resin composition according to claim 3 , wherein the resin composition exhibits a tensile strength of 6.0 MPa or more after being cured.7. The resin composition according to claim 1 , wherein the component (B) is contained in an amount of 0.5 to 100 parts by mass based on 100 parts by mass of the component (A).8. The resin composition according to claim 2 , wherein the component (B) is contained in an amount of 0.5 to 100 parts by mass based on 100 parts by mass of the component (A).9. The resin composition according to claim 1 , further comprising (E) an inorganic filler.10. The resin composition according to claim 9 , wherein the inorganic filler is silica and is contained in an amount of 20 to 96 mass % in the resin composition.11. A resin film composed of the resin composition according to .12. A resin film composed of the resin composition according to .13. A resin film composed of the resin composition according to .14. A resin film composed of the resin composition according to .15. A resin film composed of the resin composition according to .16. The resin film according to claim 11 , wherein the resin film exhibits a tensile strength of 6.0 MPa or more after being cured.17. A semiconductor laminate comprising a cured material of the resin film according to on a semiconductor wafer.18. A semiconductor device claim 17 , characterized in that the ...

RESIN COMPOSITION, RESIN FILM, SEMICONDUCTOR LAMINATE, METHOD FOR MANUFACTURING SEMICONDUCTOR LAMINATE, AND METHOD FOR MANUFACTURING SEMICONDUCTOR DEVICE

The present invention is a resin composition including: (A) an epoxy resin; (B) an epoxy compound shown by the following formula (1) and/or formula (2); (C) an epoxy compound shown by the following formula (3); (D) a phenolic curing agent; and (E) a curing accelerator, 2. The resin composition according to claim 1 , wherein the component (A) is a silicone-modified epoxy resin.4. The resin composition according to claim 1 , wherein the resin composition exhibits a tensile strength of 6.0 MPa or more after being cured.5. The resin composition according to claim 2 , wherein the resin composition exhibits a tensile strength of 6.0 MPa or more after being cured.6. The resin composition according to claim 3 , wherein the resin composition exhibits a tensile strength of 6.0 MPa or more after being cured.7. The resin composition according to claim 1 , wherein the component (B) is contained in an amount of 0.5 to 100 parts by mass based on 100 parts by mass of the component (A).8. The resin composition according to claim 2 , wherein the component (B) is contained in an amount of 0.5 to 100 parts by mass based on 100 parts by mass of the component (A).9. The resin composition according to claim 1 , further comprising (F) an inorganic filler.10. The resin composition according to claim 9 , wherein the inorganic filler is silica and is contained in an amount of 20 to 96 mass % in the resin composition.11. A resin film composed of the resin composition according to .12. A resin film composed of the resin composition according to .13. A resin film composed of the resin composition according to .14. A resin film composed of the resin composition according to .15. A resin film composed of the resin composition according to .16. The resin film according to claim 11 , wherein the resin film exhibits a tensile strength of 6.0 MPa or more after being cured.17. A semiconductor laminate comprising a cured material of the resin film according to on a semiconductor wafer.18. A ...

CURING COMPOSITION

Excellent adhesiveness to resin substrates is provided even with a reduced pretreatment, preferably without a pretreatment, by a curable composition comprising an urethane prepolymer (A) having a polyoxyalkylene backbone and an isocyanate group, and an urethane prepolymer (B) having a polycarbonate and/or polyester backbone and an isocyanate group. 1. A curable composition comprising an urethane prepolymer (A) having a polyoxyalkylene backbone and an isocyanate group , and an urethane prepolymer (B) having a polycarbonate and/or polyester backbone and an isocyanate group.2. The curable composition according to claim 1 , wherein the number average molecular weight of the urethane prepolymer (A) is 1000 or more.3. The curable composition according to claim 1 , wherein the number average molecular weight of the urethane prepolymer (B) is 4000 or less.4. The curable composition according to claim 1 , wherein the ratio of the number average molecular weight of the urethane prepolymer (B) to the number average molecular weight of the urethane prepolymer (A) ((Mn of the urethane prepolymer (B))/(Mn of the urethane prepolymer (A))×100%) is less than 100%.5. The curable composition according to claim 1 , wherein the urethane prepolymer (A) comprises a reaction product of polyoxyalkylene polyol with a polyisocyanate (a) claim 1 , andwherein the urethane prepolymer (B) comprises a reaction product of a polycarbonate polyol and/or a polyester polyol with a polyisocyanate (b).6. The curable composition according to claim 5 , wherein the polycarbonate polyol and/or the polyester polyol is aliphatic.7. The curable composition according to claim 5 , wherein the polyisocyanate (a) and/or the polyisocyanate (b) is aliphatic.8. The curable composition according to claim 1 , comprising a silicone additive (C).9. The curable composition according to claim 8 , wherein the silicone additive (C) is a polyether-modified silicone.10. The curable composition according to claim 9 , wherein the ...

HYDROPHILIC CYCLODEXTRIN-CONTAINING SILICONE GELS

Solvent-swollen crosslinked silicone gels containing covalently bonded cyclodextrin groups are prepared by hydrosilylation. The swollen gels are storage stable, compatible with water and polar solvents, and display a significant water break effect. 1. A solvent swollen hydrophilic silicone gel composition comprising: (A) optionally, a cyclodextrin reactant comprising a cyclodextrin or cyclodextrin derivative which has been modified to contain an organic group containing aliphatic unsaturation or an organic group containing silicon-bonded hydrogen;', '(B) optionally, an organopolysiloxane having at least one aliphatically unsaturated group;, 'a crosslinked silicone elastomer containing at least one covalently bonded cyclodextrin moiety, prepared by hydrosilylative crosslinking of reactants (A), (B), and (C)'} (C) an organopolysiloxane containing at least one silicon-bonded hydrogen atom, the hydrosilylative crosslinking being effected by hydrosilylating aliphatically unsaturated groups of (A), when present, and (B), by means of silicon-bonded hydrogen atoms of (A), when present, and (C), in the presence of a hydrosilylation catalyst (D), wherein at least one cyclodextrin moiety is present among reactants (A), (B), and (C),', 'and wherein the hydrosilylative crosslinking is conducted in the presence of a swelling solvent, forming a swollen hydrophilic silicone gel or the hydrosilylative crosslinking is conducted without swelling solvent and a crosslinked elastomer formed in the hydrosilylative crosslinking is dispersed into a swelling solvent to form a swollen hydrophilic silicone gel., 'wherein component (B) is not optional when component (A) is not present or where component (A) contains no aliphatic unsaturation;'}2. The solvent swollen hydrophilic silicone gel composition of claim 1 , wherein hydrosilylative crosslinking is effected in the presence of swelling solvent.3. The solvent swollen hydrophilic silicone gel composition of claim 1 , wherein cyclodextrin ...

CURABLE WATER-SWELLING WATERSTOP MATERIAL, WATERSTOP STEEL SHEET PILE, WATERSTOP STEEL SHEET PILE PRODUCTION METHOD, AND WATER-STOPPING METHOD

A curable water-swelling water stop material including: 100 parts by mass of a resin component which includes 40 to 100 parts by mass of a curable resin having a hydrolysable alkoxysilyl group and 0 to 60 parts by mass of a polyether polyol; 0.3 to 25 parts by mass of an aminosilane coupling agent; 20 to 250 parts by mass of a water-absorbent resin; and 0 to 160 parts by mass of an extender pigment, in which the hydrolysable alkoxysilyl group having a structure represented by Formula (1) —X—CH—SiR(OR), in which X is a bonding functional group having a heteroatom with an unshared electron pair and bonding to a methylene group bonding to a silicon atom of a hydrolysable silicon group, Rand Rare C-Calkyl groups respectively, and Y is 0, 1 or 2. 2. The curable water-swelling water stop material according to wherein the water-absorbent resin (D) is at least one selected from the group consisting of a polyethylene oxide resin claim 1 , a carboxymethyl cellulose alkali metal salt and a polyacrylic acid alkali metal salt.3. The curable water-swelling water stop material according to wherein the extender pigment (E) is silicon.4. A water stop steel sheet pile comprisinga coating film located on a joint portion of a steel sheet pile,{'claim-ref': {'@idref': 'CLM-00001', '#text': 'claim 1'}, '#text': 'wherein the coating film includes the curable water-swelling water stop material according to .'}5. A method of manufacturing a water-swelling steel sheet pile comprising:{'claim-ref': {'@idref': 'CLM-00001', '#text': 'claim 1'}, '#text': 'a coating step of coating the curable water-swelling water stop material according to onto a joint portion of a steel sheet pile; and'}a coating film forming step of curing the curable water-swelling water stop material to form a coating film.6. A method of stopping water comprising:{'claim-ref': {'@idref': 'CLM-00001', '#text': 'claim 1'}, '#text': 'a driving/pressing-in step of driving or pressing at least a part of a water stop steel sheet ...

ONE-PACK ADDITION CURABLE SILICONE COMPOSITION, METHOD FOR STORING SAME, AND METHOD FOR CURING SAME

Provided are a one-pack addition curable silicone composition compatible with both a good long-term storage property at room temperature under conditions whereby air is blocked to a constant level and the advance of an addition curing reaction at room temperature by being applied in a thin film of μm or less and exposed to air, which could not be obtained by conventional curable heat-dissipating grease, and a method for storing the same, and a method for curing this composition. A one-pack addition curable silicone composition having as essential ingredients: (A) organopolysiloxane having silicon-atom-bonded aliphatic unsaturated hydrocarbon groups and a specific kinematic viscosity; (B) one or more thermally conductive fillers selected from metals, metal oxides, metal hydroxides, metal nitrides, metal carbides, and allotropes of carbon; (C) organohydrogenpolysiloxane; and (D) a platinum group metal complex having an organic phosphorus compound represented by formula (1) This application is a Divisional of U.S. Pat. Application No. 15/529,302 filed on May 24, 2017, which is the National Phase of PCT/JP2015/079667 filed Oct. 21, 2015, which claims priority under 35 U.S.C. § 119(a) to Patent Application No. 2014-237302 filed in Japan on Nov. 25, 2014, all of which are hereby expressly incorporated by reference into the present application.This invention relates to a one-pack addition curable silicone composition. More particularly, it relates to a one-pack addition curable silicone composition for providing a highly heat conductive silicone grease, which meets both long-term storage stability at room temperature under limited air-shutoff conditions and the progress of addition cure reaction at room temperature when it is applied as a thin film of up to 1,500 μm and exposed to air, a method for storing the composition, and a method for curing the composition.It is well known that electronic parts such as semiconductor packages generate heat during operation and ...

INK COMPOSITION FOR COSMETIC CONTACT LENSES

Provided are ink compositions for making cosmetic contact lenses, as well as cosmetic contact lenses and methods for their preparation and use. The ink composition comprises: (a) a colorant; and (b) a nonreactive hydrophilic polymer. 1. An ink composition for making cosmetic contact lenses , the ink composition comprising: (a) a colorant; and (b) a nonreactive hydrophilic polymer; and optionally (c) a binder polymer.2. The ink composition of wherein the nonreactive hydrophilic polymer comprises a polyamide.3. The ink composition of wherein the nonreactive hydrophilic polymer comprises: dextran claim 1 , poly(ethylene oxide) claim 1 , polyvinyl alcohol (PVA) claim 1 , poly (N-isopropylacrylamide) claim 1 , poly(oligoethylene oxide) claim 1 , polyethylene glycol (PEG) claim 1 , poly (N claim 1 ,N-dimethylaminoethyl acrylate) claim 1 , poly(imine) claim 1 , poly(acrylic acid) claim 1 , or mixtures of two or more thereof.4. The ink composition of wherein the optional binder polymer comprises a copolymer formed from a hydrophilic monomer comprising functionality selected from the group consisting of hydroxyalkyl claim 1 , aminoalkyl claim 1 , and mixtures thereof; a silicone-containing macromer; and optionally a silicone-containing monomer.5. The ink composition of claim 1 , further comprising (d) a solvent.6. The ink composition of wherein the solvent comprises: ethanol claim 5 , 1-propanol claim 5 , 2-propanol claim 5 , 1-ethoxy-2-propanol (1E2P) claim 5 , t-butyl alcohol claim 5 , t-amyl alcohol claim 5 , and 3 claim 5 ,7-dimethyl-1 claim 5 ,7-octanediol (D30) claim 5 , tripropylene glycol methyl ether (TPME) claim 5 , isopropyl lactate (IPL) claim 5 , 1-(2-hydroxy ethyl)-2-pyrrolidone (HEP) claim 5 , glycerol or mixtures of two or more thereof.7. The ink composition of wherein the nonreactive hydrophilic polymer comprises a cyclic polyamide.8. The ink composition of wherein the colorant comprises: pthalocyanine blue claim 1 , pthalocyanine green claim 1 , carbazole ...

Application of self-healing material in 3d printing

The present invention provides application of a self-healing material in 3D printing. In the present invention, a self-healing material is taken as a 3D printing material, and the material is intelligently detected and spontaneously healed by utilizing a self-healing function of the self-healing material, so that a potential damage to the self-healing material caused by generated micro-cracks can be prevented. Compared with molding conditions of a product, gentle and mild conditions are required for self-healing, and the overall performance of the product cannot be affected from beginning to end of a self-healing process, thereby reducing the maintenance cost of the product, prolonging the service life of the product, and increasing the utilization rate of resources.

GRADIENT ELECTRICALLY CONDUCTIVE-UNIFORM THERMALLY CONDUCTIVE DUAL NETWORK STRUCTURE-BASED ELECTROMAGNETIC SHIELDING POLYMER COMPOSITE WITH LOW REFLECTION AND HIGH ABSORPTION

A gradient electrically conductive-uniform thermally conductive dual network structure-based electromagnetic shielding polymer composite with low reflection and high absorption and a preparation method thereof. The electromagnetic shielding polymer composite includes a gradient conductive carbon nanotube network with a vertically oriented cell structure and a uniformly thermally conductive hexagonal boron nitride/carbon nanotube network constructed by the hexagonal boron nitride dispersed uniformly in the carbon nanotube network and the gradient carbon nanotube network. The gradient electrically conductive carbon nanotube network and the uniformly thermally conductive hexagonal boron nitride/carbon nanotube network form a composite synergistic dual function network structure so as to make the electromagnetic shielding polymer composite have a low reflection and high absorption and excellent thermal conductivity. 1. An electromagnetic shielding polymer composite based on a gradient electrically conductive-uniform thermally conductive dual network structure , comprising:a gradient electrically conductive carbon nanotube network with a vertically oriented cell structure; anda uniform thermally conductive hexagonal boron nitride/carbon nanotube network constructed by a hexagonal boron nitride dispersed uniformly in the carbon nanotube network and the gradient carbon nanotube network;wherein the gradient electrically conductive carbon nanotube network and the uniform thermally conductive hexagonal boron nitride/carbon nanotube network form a composite synergistic dual function network structure.2. A method for preparing the electromagnetic shielding polymer composite of claim 1 , comprising:(S1) blending different portions of a carbon nanotube respectively with a waterborne polyurethane in deionized water followed by ultrasonic dispersion to obtain multiple dispersions with different carbon nanotube contents; andpouring the multiple dispersions with different carbon ...

High-RI siloxane monomers, their polymerization and use

Phenoxyphenylsilane monomers were synthesized and polymerized. The polymers have high refractive indices and excellent UV and thermal stability. Their water and oxygen permeability is lower than commercial phenyl silicone elastomers. They show good compatibility with metal oxide nanoparticles. The polymers of the invention are suitable as LED encapsulant, as light guide material in CMOS image sensors, in OLED devices, lasers and in other optical applications.

Organopolysiloxane, production method thereof, and curable silicone composition

An organopolysiloxane represented by the following average unit formula: (R 1 SiO 3/2 ) a (XR 2 2 SiO 1/2 ) b (O 1/2 SiR 2 2 —Y—R 2 2 SiO 1/2 ) c is provided. R 1 and R 2 each individually represent a C 1 -C 20 alkyl group, C 6 -C 20 aryl group, or C 7 -C 20 aralkyl group. X represents a C 2 -C 12 alkenyl group or a siloxane residue and Y represents a siloxane linking group. Alternatively X represents a C 2 -C 12 alkenyl group or a silphenylene residue and Y represents a silphenylene linking group. Subscript “a” is a number in a range of 0.65 to 0.90, “b” is a number in a range of 0.10 to 0.35, “c” is a number in a range of 0 to 0.10, and “a”+“b”+“c”=1.00. The organopolysiloxane has a siloxane residue or silphenylene residue having a silicon atom-bonded hydrogen atom in an organopolysiloxane resin block. The organopolysiloxane generally exhibits high refractive index and high transparency as well as excellent handleability

ROOM TEMPERATURE-CURABLE ORGANOPOLYSILOXANE COMPOSITION AND CURED PRODUCT THEREOF

Provided is a room temperature-curable organopolysiloxane composition that is superior in fast curably, can form a cured product superior in storage stability and durability, and can further be produced in an industrially advantageous manner using more highly versatile materials. 2. The room temperature-curable organopolysiloxane composition according to claim 1 , further comprising:(D) a hydrolyzable organosilane and/or a partial hydrolysis condensate thereof other than the components (A) and (B), in an amount of 0 to 30 parts by mass per 100 parts by mass of the component (A);(E) a filler in an amount of 0.1 to 1,000 parts by mass per 100 parts by mass of the component (A); and(F) an adhesion promoter in an amount of 0.001 to 30 parts by mass per 100 parts by mass of the component (A).4. A sealing agent claim 1 , coating agent or adhesive agent containing the room temperature-curable organopolysiloxane composition according to .5. A molded product comprised of a cured product of the room temperature-curable organopolysiloxane composition according to . The present invention relates to a room temperature-curable organopolysiloxane composition and an elastomer-shaped molded product (silicone rubber cured product) obtained by curing such room temperature-curable organopolysiloxane composition. Particularly, the present invention relates to: a room temperature-curable organopolysiloxane composition containing, as a curing agent (cross-linking agent), a bissilyl-type hydrolyzable organic silicon compound having two hydrolyzable silyl groups in its molecule and a structure where two silicon atoms in such hydrolyzable silyl groups are bonded to each other through a carbon-carbon double bond and/or a partial hydrolysis condensate thereof (hydrolyzable siloxane oligomer); and to an elastomer-shaped molded product (silicone rubber cured product) obtained by curing this room temperature-curable organopolysiloxane composition.Conventionally, there have been known various ...

Field effect-transistor, method for manufacturing same, wireless communication device using same, and product tag

A field-effect transistor including at least: a substrate; a source electrode; a drain electrode; a gate electrode; a semiconductor layer in contact with the source electrode and with the drain electrode; and a gate insulating layer insulating between the semiconductor layer and the gate electrode, wherein the semiconductor layer contains a carbon nanotube, and the gate insulating layer contains a polymer having inorganic particles bound thereto. Provided is a field-effect transistor and a method for producing the field-effect transistor, wherein the field-effect transistor causes decreased leak current and furthermore enables a semiconductor solution to be uniformly applied.

LOW-VISCOSITY PHOTOCURABLE ADHESIVE COMPOSITIONS

Photocurable (meth)acrylate compositions with low viscosity when uncured, and high flexibility and shear/tensile strength when cured, further possessing rapid tack-free fixture times, comprising mixtures of urethane acrylate resin, isobornyl acrylate, N,N-dimethylacrylamide, a photoinitiator component, and a low percentage of tetrahydrofurfuryl acrylate, for example from about 9% to about 15% by weight based on the weight of the composition. Applications can include adhesive bonding of medical tubing, UV/Visible transparent plastics material medical devices or equipment, or other flexible UV/Visible transparent material substrates. 1. A photocurable (meth) acrylate composition comprising:(i) tetrahydrofurfuryl acrylate;(ii) urethane acrylate resin;(iii) isobornyl acrylate;(iv) N,N-dimethylacrylamide; and(v) a photoinitiator component.2. The photocurable (meth) acrylate composition according to claim 1 , wherein the composition has a viscosity at 25° C. of less than about 550 mPa·s.3. The photocurable (meth) acrylate composition according to claim 1 , wherein the photocured (meth) acrylate composition has an elongation-at-break value of greater than 130%.4. The photocurable (meth) acrylate composition according to claim 1 , wherein the composition has a fixture time of less than about 60 seconds claim 1 , using actinic radiation from about 365 nm to 405 nm at an intensity of 500 mW or less.5. The photocurable (meth) acrylate composition according to claim 1 , wherein the photocurable (meth) acrylate composition achieves a tack-free surface cure in less than 40 seconds claim 1 , when photocured for between 40 seconds and 0.05 seconds using actinic radiation from about 365 nm to 405 nm at an intensity of 500 mW or less.6. The photocurable (meth) acrylate composition according to claim 1 , wherein the (meth) acrylate composition when photocured has a shear strength as determined by ISO 4587 of greater than about 4 N/mm.7. The photocurable (meth) acrylate composition ...

Moisture curable compositions

Disclosed is a two-component silicone composition, which can cure via two part moisture cure organosiloxanc composition. The composition generally has which could improved cure speed while whilst maintaining good storage stability.

ONE-LIQUID-TYPE THERMOSETTING HEAT-CONDUCTIVE SILICONE GREASE COMPOSITION, AND METHOD FOR PRODUCING CURED PRODUCT THEREOF

Provided is a one-liquid-type thermosetting heat-conductive silicone grease composition which initially has low viscosity but high shape retention, which becomes soft after heat-curing, which has good adhesion to a substrate, and which can be stored at room temperature. Also provided is a method for producing a cured product of said composition. 1. A normal temperature-storable , addition one-part heat-curable , heat-conductive silicone grease composition comprising , as essential components ,(A) 100 parts by weight of an organopolysiloxane having a viscosity of 50 to 100,000 mPa·s at 25° C. and containing at least one alkenyl group per molecule,(B) a liquid organohydrogenpolysiloxane having a viscosity of up to 100 mPa·s at 25° C., containing 2 to 10 silicon-bonded hydrogen atoms (i.e., Si—H groups) per molecule, containing at least one alkoxy and/or epoxy group bonded to a silicon atom through an alkylene group, the polysiloxane having a degree of polymerization of up to 15 and a cyclic structure-containing skeleton, in such an amount that the number of Si—H groups divided by the number of alkenyl groups in the composition falls in the range from 0.1 to 5,(C) an effective amount of a photoactive platinum complex curing catalyst selected from the group consisting of trimethyl(acetylacetonato)platinum complex, trimethyl(2,4-pentanedionate)platinum complex, trimethyl(3,5-heptanedionate)platinum complex, trimethyl(methylacetoacetate)platinum complex, bis(2,4-pentanedionato)platinum complex, bis(2,4-hexanedionato)platinum complex, bis(2,4-heptanedionato)platinum complex, bis(3,5-heptanedionato)platinum complex, bis(1-phenyl-1,3-butanedionato)platinum complex, bis(1,3-diphenyl-1,3-propanedionato)platinum complex, (1,5-cyclooctadienyl)dimethyl platinum complex, (1,5-cyclooctadienyl)diphenyl platinum complex, (1,5-cyclooctadienyl)dipropyl platinum complex, (2,5-norbornadiene)dimethyl platinum complex, (2,5-norbornadiene)diphenyl platinum complex, (cyclopentadienyl) ...

Inorganic polymer material, method for forming the same, and inorganic polymer coating produced therefrom

The present disclosure provides a method for forming an inorganic polymer material, including mixing 10 to 80 parts by weight of tetraalkoxysilane and 10 to 80 parts by weight of trialkoxysilane to form a mixture; and performing a reaction at pH of 0 to 4 by adding 5 to 30 parts by weight of a catalyst to the mixture to form an inorganic polymer material.

Ambient Cure High Temperature Protective Coating

An ambient curable coating composition includes a mixture of components comprising a polysiloxane having a Mw of at least 10,000 as determined by gel permeation chromatography using a polystyrene standard, (b) an alkoxy functional polysiloxane, and (c) an inorganic corrosion inhibitor, a method of preparing a corrosion resistant coating comprising (i) applying the coating composition to a substrate and (ii) curing component (b) at ambient conditions; and a substrate at least partially coated with the coating composition.

Curable composition for lens, lens and optical device

Provided is a curable composition capable of giving a lens that has excellent transfer accuracy from a mold and offers heat resistance and optical properties at excellent levels. The curable composition according to the present invention for lens formation contains a cycloaliphatic epoxide (A) represented by Formula (a), a cationic-polymerization initiator (B), and a polysiloxane (C) represented by Formula (c). The curable composition contains the polysiloxane (C) in an amount of 0.01% to 5% by weight based on the total amount of the curable composition. The curable composition according to the present invention for lens formation may further contain a siloxane compound (D) containing two or more epoxy groups per molecule.

Organopolysiloxane emulsion composition for release paper or release film, method for producing same, and release paper and release film

An organopolysiloxane emulsion composition for release paper or a release film, said composition being produced by dispersing a mixture comprising components (A) to (D) as mentioned below in water: (A) an alkenyl-group-containing diorganopolysiloxane having at least two alkenyl groups per molecule and having a viscosity of 1,000 Pa·s or less at 25° C., in an amount of 100 parts by mass; (B) an organohydrogenpolysiloxane having at least two Si—H groups per molecule and having a viscosity of 1 Pa·s or less at 25° C., in such to an amount that the number of moles of an Si—H group can become 0.5 to 10 times the number of moles of an alkenyl group in the component (A); (C) a curing catalyst, in an amount of 0.01 to 3 parts by mass; and (D) a polyether-modified and/or polyol-modified organosilicon compound, in an amount of 0.01 to 10 parts by mass.