СОДЕРЖАЩИЙ ГИДРОКСИЛЬНЫЕ ГРУППЫ МЕТИЛСТИРОЛ И ПОЛИМЕРЫ НА ЕГО ОСНОВЕ

Изобретение относится к эластомерным композициям, содержащим один или более армирующих наполнителей. Описан способ получения соединения полимера, содержащего мономерное звено полиена, включающий а) анионное инициирование полимеризации по меньшей мере одного типа полиена и соединения, имеющего общую формулугде m означает целое число от 2 до 5, и каждая группа Gнезависимым образом является защитной группой, причем указанный, по меньшей мере, один тип полиена полимеризуют до полимеризации указанного соединения, и где число звеньев, получаемых из указанного соединения, равно от 1 до 10, с получением, таким образом, полимера, и b) одно из тушения полимера, реакции полимера с соединением, обрывающим рост цепи, или полимеризации дополнительных количеств указанного по меньшей мере одного типа полиена. Технический результат: улучшение параметров сцепления с дорогой и сопротивление качению. 11 з.п. ф-лы, 7 табл.

ОГНЕСТОЙКИЕ ВИНИЛОВЫЕ ПОЛИМЕРЫ

Изобретение относится к виниловым полимерам с соответствующими полимерными характеристиками для применения в качестве ингибиторов горения. Виниловые полимеры для применения в качестве ингибиторов горения содержат галогенгидрин и эпоксигруппы, полимеры имеют средневзвешенную молекулярную массу (Mw) по меньшей мере 40000 Да, содержание галогена в диапазоне от 0,6 до 55 мас.%, такое содержание оксирановых групп, что содержание кислорода оксиранового цикла находится в диапазоне от 1 до 3 мас.% по отношению к содержанию галогена, и демонстрирующие потерю массы 5% при температуре по меньшей мере 240°С. Заявлена также огнестойкая полимерная композиция и применение виниловых полимеров в качестве ингибитора горения в полимерных композициях. Технический результат – полученные композиции прошли испытания на огнестойкость и показали соответствие классу V2. 4 н. и 9 з.п. ф-лы, 4 пр.

БРОМИРОВАННЫЕ ПОЛИМЕРЫ В КАЧЕСТВЕ ПЛАМЯГАСИТЕЛЕЙ И СОДЕРЖАЩИЕ ИХ ПОЛИМЕРНЫЕ СИСТЕМЫ

Изобретение относится к препятствующим воспламенению добавкам для органических полимеров. Пламегасящая полимерная композиция включает горючий полимер, смешанный в ней с бромированной пламегасящей добавкой, выбранной из числа одного или нескольких приведенных ниже соединений: (i) сополимера, содержащего стирольные и 2,3-дибромпропилмалеинимидные повторяющиеся звенья; (ii) бромированного сложного полиэфира, содержащего связанные с алифатическими группами атомы брома; (iii) простого аллилового эфира бромированной по кольцу новолачной смолы; (iv) простого 3-бром-2-гидроксипропилового эфира новолачной смолы; (v) простого 2,3-дибромпропилового эфира крезолноволачной смолы, и (vi) бромированного полимера или сополимера, полученного методом ROMP. Изобретение обеспечивает устойчивость пламегасящей добавки при повышенных температурах, низкую токсичность и исключение значительных потерь физических свойств полимера при ее применении. 6 з.п. ф-лы, 10 пр.

СПОСОБ ПОЛУЧЕНИЯ СПОСОБНОГО ВСПЕНИВАТЬСЯ ПОЛИСТИРОЛА

... 1. Способ получения способных вспениваться полимеров стирола с молекулярным весом Mw более чем 170.000 г/моль, отличающийся тем, что содержащий вспенивающий агент расплав полимера стирола с температурой в интервале от 140 до 300°С пропускают через сопловую плиту с отверстиями, диаметр которых на выходе сопла составляет максимально 1,5 мм, и затем гранулируют. 2. Способ по п.1, отличающийся тем, что способный вспениваться полимер стирола имеет молекулярный вес в интервале от 190.000 до 400.000 г/моль. 3. Способ по п.1 или 2, отличающийся тем, что способный вспениваться полимер стирола имеет молекулярный вес с неоднородностью Mw/Mn максимально 3,5. 4. Способ по п.1 или 2, отличающийся тем, что в качестве полимера стирола применяют чистый как стекло полистирол (GPPS), ударопрочный полистирол (HIPS), акрилнитрил-бутадиен-стирол-полимеризаты (ABS), стирол-акрилнитрил (SAN) или их смеси или смеси с простым полифениленовым эфиром (РРЕ). 5. Способ по п.1 или 2, отличающийся тем, что содержащий ...

АНТИПИРЕНОВАЯ КОМПОЗИЦИЯ ДЛЯ ПРИМЕНЕНИЯ В ПОЛИСТИРОЛАХ

... 1. Способ замедления воспламенения стирольных смол и вспененных стирольных смол, включающий введение эффективного количества, по меньшей мере, одного антипиренового соединения, содержащего как алифатический, так и ароматический атом брома, выбранного из группы, включающей ! ! 2. Способ по п.1, где антипиреновое соединение имеет ПКИ больше, чем 26 при 5 ч./100 ч. смолы и 5% потерю массы по ТГА выше 215°С. ! 3. Промышленное изделие, содержащее композицию стирольной смолы или композицию вспененной стирольной смолы, где указанная композиция содержит эффективное количество, по меньшей мере, одного антипиренового соединения по пп.1, 2.

ПОЛИМЕРНАЯ КОМПОЗИЦИЯ, ПОЛИМЕР, СПОСОБ ПОЛУЧЕНИЯ КОМПОЗИЦИИ, ПРОДУКТ

Биосовместимость многих полимеров улучшается при смешивании с ними полимера, включающего цвиттер-ионные группы. Обычно цвиттер-ионная группа представляет собой аммоний-фосфатную эфирную цвиттер-ионную группу, и полимер, содержащий ее, может быть получен путем свободно-радикальной полимеризации этилен-ненасыщенных мономеров, включая мономер, содержащий цвиттер-ионную группу. Смешение двух полимеров можно осуществить путем сухого смешивания полимерных частиц или путем перемешивания полимеров в жидкой дисперсной системе или в растворе с последующим удалением жидкой среды. Абсорбцию фибриногена и/или активацию тромбоцитов полимерами ножно снизить до величин, составляющих менее 80% или менее 60% от базового полимера, путем введения полимера, содержащего цвиттер-ионную группу, в количестве более 10% или более 30%. Предпочтительными композициями являются сополимеры внутренней соли -2-(метакрилоилоксиэтил)-2'-(триметиламмоний)этилфосфата с высшим алкил(мет)акрилатом, смешанные с олефиновыми полимерами ...

Термопластичная формовочная композиция

Frei fliessende Pulverzusammensetzung, Verfahren zu ihrer Herstellung und daraus abgeleitete homogene Schicht

VERTRAEGLICHE POLYMERMISCHUNGEN

Thermoplastische Harzmischung.

Thermoplastische Harzmischung.

PFROPFCOPOLYMER UND STYROLHARZ-ZUSAMMENSETZUNG.

POLYMERE ZUSAMMENSETZUNG, VERFAHREN ZU IHRER HERSTELLUNG UND THERMOPLASTISCHE POLYMERE ZUSAMMENSETZUNG.

Strukturierte Polyacetalharzzusammensetzung sowie Verfahren zu ihrer Herstellung

Expandierbare Styrolpolymerisate, enthaltend als Treibmittel Kohlendioxid

Harzzusammensetzung auf Styrolbasis und Verfahren zur Herstellung von Formmassen

OELBESTAENDIGE KAUTSCHUKMISCHUNG.

VINYL-HARZ-ZUSAMMENSETZUNG.

THERMOPLASTISCHE FORMMASSEN AUF DER BASIS VON OLEFIN-ACRYLSAEUREESTER-COPOLYMERISATEN

Polystyrene moulding materials with improved flow properties - contain anionic polystyrene with mol. wt. 50,000-150,,000 and narrow mol. wt. distribution, and 1-20 wt. per cent paraffin oil of mol. wt. 500

Moulding materials (I) are claimed, contg. 80-99 wt.% styrene- and/or substd. styrene-contg. polymer (A) with mean mol. wt. 50,000-150,000 and a narrow mol. wt. distribution, and 1-20 wt.% lubricant (B). Pref. (A) is polystyrene produced by anionic polymerisation, and (B) is paraffinic white oil with mean mol. wt. 500. Pref., (A) has mean mol. wt. 80,000-110,000, with U = M/Mn - 1 = less than 0.1, and is prepd. as described, e.g. in EP341620. Amt. of (B) is 1.5 - 10 wt.%. USE/ADVANTAGE - W.r.t. conventional polystyrene/lubricant compsns., (I) have markedly better flow properties, combined with at least as good impact strength and heat distortion temp.

Schwerentflammbare, ein Styrolpolymerisat enthaltende Formmassen

HOLZMEHLGEFUELLTE THERMOPLASTISCHE FORMMASSEN MIT VERBESSERTEN VERARBEITUNGSEIGENSCHAFTEN

VERFAHREN ZUM IMPRÄGNIEREN VON HOLZ

Styrene polymers

A polymer of styrene containing at least 50% by weight of styrene units has associated therewith 0.5-6.0% of polyvinyl bromide as a flame-proofing agent. The polymer may be foamed. The polymer may be produced by dispersing finely divided polyvinyl bromide in a mixture of polystyrene, styrene and petroleum ether (as expanding agent) and polymerizing in the presence of lauroyl peroxide to form polystyrene granulate which is then expanded by heating. Alternately, the polymer may be produced by rolling polystyrene containing pentane (as expanding agent) around a suspension of polyvinyl bromide and polyisobutylene in pentane, evaporating the pentane to form polystyrene granulate coated with a film of polyisobutylene containing polyvinyl bromide and then expanding the polystyrene by heating.ALSO:Granules of a polymer of styrene containing at least 50% by weight of styrene units are coated with polyvinyl bromide to produce a flame-resistant polymer. The styrene polymer may contain an expanding ...

NEW MATERIALS

LAMINATES

... 1357950 Thermoplastic resin laminates BADISCHE ANILIN- & SODA-FABRIK AG 6 Oct 1971 [7 Oct 1970] 46436/71 Heading B5N [Also in Division B2] A laminate of two or more different thermoplastics plies has at least one ply comprising a mixture composed of (a) a homopolymer or copolymer of a vinylaromatic monomer, (b) a homopolymer or copolymer of an olefin monomer, and (c) a block copolymer (A-B) in which A is a polyvinylaromatic polymer (molecular weight 10,000 to 150,000) and B is a polyolefin (molecular weight 10,000 to 200,000) having not more than 10% of its C-C bonds olefinically unsaturated and in which A : B is 10 : 90 to 70 : 30, in which mixture the ratio of (a) to (b) is 4 : 1 to 1 : 4 and (c) forms from 5 to 70% of the mixture. Component (a) of the mixture may be a homopolymer of styrene, a copolymer of styrene with other monomers such as -methylstyrene or maleic anhydride, a graft copolymer of styrene or a mixture of the above polymers. The impact resistance of the component (a) ...

HYDROCARBON-DERIVED RESIN

... 1413489 Adhesive coatings GOODYEAR TIRE & RUBBER CO 12 Dec 1972 [20 Jan 1972] 57266/72 Heading B2E [Also in Division C3] Tetrapolymer resins derived from piperylene, -methylstyrene, 2-methyl-2-butene and dicyclopentadiene are used in combination with (a) a natural or synthetic rubber to produce a pressure-sensitive adhesive or (b) a thermoplastic polymer (certain alphamonoolefin polymers) to produce a hot-melt adhesive. In the latter case part of the polymer may be replaced by paraffin wax and/or micro-crystalline wax. Examples refer to blends of the tetrapolymer with butadiene-styrene or natural rubber coated from solution on to a polyethylene terephthalate film and to blends with ethylene-vinyl acetate copolymer and paraffin wax coated from the melt on to corrugated cardboard.

Graft copolymers and blends thereof with polyolefins

A novel graft copolymer capable of imparting to a polyolefin when blended therewith a good balance of tensile modulus, sag resistance and melt viscosity, is a polyolefin trunk having a, preferably relatively high weight-average molecular weight, methacrylate polymer chain grafted thereto. The graft copolymer is formed by dissolving a non-polar polyolefin in an inert hydrocarbon solvent, and, while stirring the mixture, adding methacrylate monomer together with initiator to produce a constant, low concentration of radicals, and covalently graft a polymer chain, preferably of relatively high molecular weight, to the polyolefin backbone. The graft copolymer can be separated from the solvent, by volatilizing the solvent, for example in a devolatilizing extruder, and pelletised or extruded or otherwise shaped into a desired shape such as a sheet, tube or the like. This graft copolymer can be blended with a polyolefin matrix to improve its physical properties in the melt, upon cooling, and in ...

Composition for use in the solubilisation of hydrophobic active agents

A composition comprising a lipid and a copolymer of styrene and maleic acid, wherein the ratio of styrene to maleic acid monomer units is greater than 1:1, wherein the polymer and lipid are in the form of macromolecular assemblies. The composition finds use in the solubilisation of hydrophobic active agents.

Compositions

Composite particles

A process for producing composite particles comprises the steps of (i) providing an aqueous dispersion of a sol of a modified finely divided solid, (ii) adding at least one monomer suitable for free radical type polymerisation, and (iii) adding a free radical polymerisation initiator to initiate polymerisation of the monomer, wherein the reaction mixture is free from added surfactant, dispersant and/or auxiliary comonomer. The monomer preferably comprises at least one ethylenically unsaturated group and may comprise styrene. The finely divided solid may be an epoxysilane-modified silica and the initiator may be a cationic azo initiator. An aqueous composition containing composite particles is also disclosed, which comprises a modified finely divided solid and a copolymer formed by polymerising styrene and an ester of an ethylenically unsaturated mono- or dicarboxylic acid with a C1-12 alkanol. A paint or coating composition comprising the composite particles is also claimed.

Golf balls

COMPATIBLE POLYMER BLENDS

Improved thermoplastic styrene polymer composition

A thermoplastic styrene polymer composition having excellent mechanical and processing properties is presented. This composition contains: (A) 1 through 99% by weight of a component A consisting essentially of at least one styrene polymer selected from the group consisting of polystyrene and styrene-containing polymers having a weight-average molecular weight of 50,000 through 500,000; and (B) 99 through 1% by weight of a component B consisting essentially of at least one ionically crosslinked product of at least one modified block copolymer with at least one univalent, bivalent or trivalent metal ion, said modified block copolymer comprising a block copolymer of at least one aromatic vinyl compound and at least one conjugated diene compound onto which at least one molecular unit containing at least one dicarboxylic acid group or the derivative thereof is grafted.

Flame retardant vinylic resin comprising non-halogenated flame retardants and method for preparing the same

IMPROVED THERMOPLASTIC RESIN COMPOSITION

... 1286178 Graft polymer compositions SUMITOMO CHEMICAL CO Ltd 23 Oct 1970 [29 Oct 1969] 50453/70 Heading C3G A thermoplastic resin composition comprises 1-99, preferably 20-95, parts by weight of an acrylic resin, 99-1, preferably 80-5, parts by weight of a styrene resin and a graft copolymer of ethylene/vinyl acetate copolymer with vinyl chloride which is present in an amount of 1-50, preferably 5-50, parts by weight per 100 parts by weight of the combined acrylic and styrene resins. The graft copolymer is preferably one in which 30-90% by weight is an ethylene/vinyl acetate copolymer backbone containing vinyl acetate in an amount 20-90% by weight and 70-10% by weight is vinyl chloride graft polymerized on to said backbone. Such graft copolymers may be produced under radical polymerization conditions. The acrylic resin may be polymethyl methacrylate or a copolymer of methyl methacrylate with a vinyl monomer such as acrylonitrile, N-allyl-maleimide, a C 1-8 alkyl acrylate (e.g. methyl acrylate ...

IMPACT-RESISTANT THERMOPLASTIC MOULDING MATERIALS

... 1328446 Impact-resistant moulding materials BADISCHE ANILIN- & SODA-FABRIK AG 19 April 1971 [29 Jan 1970] 20532/71 Headings C3G and C3P An impact-resistant thermoplastic moulding material comprises a mixture of: (A) from 70 to 99% by weight based on the weight of (A) plus (B) of a homopolymer of styrene or of a copolymer of styrene with up to 60% by weight based on the weight of (A) of a styrene derivative bearing a substituent on the nucleus and/or on the vinyl side chain; and (B) from 30 to 1% by weight based on the weight of (A) plus (B) of a soft component consisting of: (1) an - olefin polymer and (2) a substantially gel-free and uncrosslinked copolymer of a vinylaromatic compound and a diene hydrocarbon which has been prepared by a method involving anionic solution polymerization and is optionally wholly or partly hydrogenated, "Substantially gel-free and uncrosslinked" means that no more than 10% by weight of the copolymer remains as an insoluble residue when 1 part by weight of ...

Filled compositions of a polyphenylene ether resin and rubber-modified alkenyl aromatic resins.

Novel compositions are disclosed which include a polyphenylene ether resin, a rubber-modified alkenyl aromatic resin, and aluminum silicate. Also included within the scope of this invention are flame-retardant compositions of said polyphenylene ether resin, said rubber-modified alkenyl aromatic resin, and said aluminum silicate.

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.

THERMOPLASTIC POLYPHENYLENE ETHER RESIN MOULDING COMPOSITIONS

Delustered thermoplastic resin composition

A delustered thermoplastic resin composition obtained by incorporating in 100 parts by weight of a thermoplastic resin up to 40 parts by weight of a cross-linked polymer having an average particle diameter of 35-500 mu which polymer is obtained by suspension-polymerizing a non-crosslinking monomer composition comprising 50-70 wt. % of a vinyl aromatic monomer, 10-40 wt. % of at least one monomer selected from the group consisting of alkyl acrylates having 1-13 carbon atoms in the alkyl group, 10-40 wt. % of a monomer selected from alkyl methacrylates having 1-4 carbon atoms in the alkyl group and 0-40 wt. % of another monoethylenically unsaturated monomer with 0.5-5 parts by weight, per 100 parts by weight of the non-cross-linking monomer composition, of a cross-linking monomer having at least two double bonds in the molecule.

New thermoplastic compositions.

FLAME-ADVERSE RESIN COMPOSITION

THERMOPLASTIC ELASTOMER CONTAINING IN DISTRIBUTED FORM VULCANIZED INDIA RUBBER

THERMOPLASTIC RESIN COMPOSITION

SCHLAGZAHE ALTERUNGSBESTANDIGE AES-POLYMERISATE UND VERFAHREN ZU IHRER HERSTELLUNG

FLAME-PROTECTED EXPAND-CASH OF STYRENE POLYMERS AND PROCEDURES FOR YOUR PRODUCTION

EXPAND-CASH POLYSTYRENE RESIN PARTICLES AND MANUFACTURING PROCESSES FOR IT, PARTICLE AND FORM FOAM MATERIAL PRODUCT VOREXPANDIERTE

ROAD MARKING COLORS ON BASIS OF ACRYLATE RESINS AND PROCEDURE FOR YOUR PRODUCTION

PROCEDURE FOR THE PRODUCTION OF POLYFUNCTIONAL POLYMERS AND THESE CONTAINING POLYMER MASSES

FLAME-ADVERSE, THERMOPLASTIC POLYCARBONATE MOLDING MATERIALS

TRANSPARENT AND TOUGH-RIGID MOLDING MATERIALS ON BASIS OF STYRENE BUTADIENE BLOCK COPOLYMER MIXTURES

THERMOPLASTIC FLAME-ADVERSE RESIN COMPOSITIONS

GRAFTING COPOLYMERS AND MIXTURES THE SAME WITH POLYOLEFINS

THERMOPLASTIC MOLDING MATERIALS

STRUCTURED POLYACETALHARZZUSAMMENSETZUNG AS WELL AS PROCEDURE FOR YOUR PRODUCTION

COMPOSITION FOR THE INCREASE OF THE FLAME RETARDING EFFECT.

THICKENER FUER PHYSICAL DRYING ANSTRICHUND OF COATING MATERIALS AND PROCEDURES FOR THE PRODUCTION OF THE THICKENERS.

FOAMS FROM ONLY FEW INTERLACED MIXTURES OF PL AND POLYSTYRENE AND PROCEDURES FOR THE PRODUCTION.

THERMOPLASTIC ELASTOMERS COMPOSITIONS AND PROCEDURES FOR THEIR PRODUCTION.

PROCEDURE FOR THE PRODUCTION OF RECYCLAT ABSTENTIONS, EXPAND-CASH STYRENE POLYMERS

PROCEDURE FOR THE PRODUCTION FROM MATERIAL TO EXTRUSIONSFORMEN.

WITH FUNKTIONALISIERTEN POLYMERS IMPACTTOUGHLY MODIFIED THERMOPLASTICS AND THEIR USE FOR THE PRODUCTION OF SHAPED PARTS.

Polymerisatgemisch

FLAMING CELEBRATIONS RESIN COMPOSITION

SCHLAGZAHE ALTERUNGSBESTANDIGE AES POLYMERS AND PROCEDURES FOR YOUR PRODUCTION

PROCEDURE FOR THE PRODUCTION OF POLYFUNCTIONAL POLYMERS AND THESE CONTAINING POLYMER MASSES

LEADING PLASTIC MATERIAL AND METHOD TO ITS PRODUCTION

COMPOSITION AND PROCEDURE FOR THE PRODUCTION OF SUBSTRATES BY POWDER COPYING METHODS AND THEREBY MANUFACTURED SUBSTRATES

RESIN COMPOSITION ON STYRENE BASIS AND PROCEDURE FOR THE PRODUCTION OF MOLDING MATERIALS

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

FLAME-ADVERSE RESIN COMPOSITION

ANTISTATIC POLYMER COMPOSITIONS OF IMPROVED DUCTILITY

GRAFT COPOLYMERS AND BLENDS THEREOF WITH POLYOLEFINS

GRAFT COPOLYMER AND STYRENE BASED RESIN COMPOSITION

STYRENIC POLYMER COMPOSITES

Light lignocellulosic materials having good mechanical properties

The invention relates to a method for producing a light lignocellulosic material having an average density in the range of 200 to 600 kg/m3, and comprising, on basis of the lignocellulosic material: A) 30 to 95 wt % of lignocellulose particles; B) 1 to 25 wt % of expanded plastic particles having a bulk density in the range of 10 to 100 kg/m3; C) 3 to 50 wt % of a binding agent, selected from the group of aminoplast resin, phenol formaldehyde resin, and organic isocyanate having at least two isocyanate groups; and optionally D) additives are mixed and then pressed under increased temperature and increased pressure, characterized in that the expanded plastic particles are obtained from expandable plastic particles having a content of propellant in the range of 0.01 to 4 wt % relative to the expandable plastic particles.

Plastic foam material composed of polyolefin based resin and silane-modified polymer and method for making same

FLAME RETARDANT, NON-DRIPPING COMPOSITION OF POLYPHENYLENE ETHER AND ACRYLONITRILE - BUTADIENE-STYRENE

FLAME RETARDANT COMPOSITION

Resorbable biomimetic prosthetic ligament

The present invention relates in particular to an artificial ligament prosthesis which is notable in that it comprises a layer totally or partly consisting of PCL fibres. The ligament prosthesis according to the invention is a biodegradable and "biointegrable" artificial ligament which makes it possible to take away all the apprehensions and uncertainties due to non-degradable synthetic supports. It is a prosthetic structure inspired by and similar to the native tissue, which is biodegradable while being sterilisable. It can optionally be seeded in order to facilitate the formation of functional tissues with controlled cell and tissue activity, having the required mechanical properties. The prosthesis according to the invention is slowly resorbable in order to be gradually replaced with a functional tissue identical to that of the native ligament.

Multi-layered polymer based film structure for medical grade products

Thermoplastic Starch Composition Derives From Agricultural Waste

A thermoplastic starch composition acquired from compounding a mixture comprises starch containing agricultural waste in 45 to 70% by weight of total composition that the agricultural waste contains starch content less than 50% in dry weight; thermoplastic synthetic polymer in 5 25 to 50% by weight of total composition; plasticizer in 1 to 10% by weight of total composition; and coupling agent in 1 to 5% by weight of total composition; wherein the compounding is performed at a first temperature which is higher than room temperature.

Multi-layered polymer based moisture barrier structure for medical grade products

Method for producing polymer mixtures comprised of amino nitriles and thermoplastic polymers

Polymer compositions, polymer films, polymer gels, polymer foams, and electronic devices containing such films, gels and foams

A polymer film, polymer gel, and polymer foam each contain an electrically conductive polymer and an ionic liquid and are each useful as a component of an electronic device.

Thermoplastic polymer composition and molded product

A thermoplastic polymer composition capable of exhibiting excellent impact resistance, durability and destaticizing property containing (A) 50 to 95% by mass of an aliphatic polyester-based resin and (B) 5 to 50% by mass of a block copolymer of (B1) a hard segment block with at least one of a polyamide, polyester, polyolefin or polyurethane, and (B2) a soft segment block having an ether bond.

Uv-reflecting compositions

A composition containing polymeric particles. The polymeric particles have an average particle diameter from 30 to 300 nm and a Vicker's scale hardness from 100 to 700 Kgf/mm 2 . The composition also contains a film-forming polymer having T g no greater than 80° C. The refractive index difference between the polymeric particles and the film-forming polymer is at least 0.04.

Thermoplastic Resin Composition and Molded Product Using the Same

Provided is a thermoplastic resin composition that includes (A) a base resin including (A-1) a polycarbonate resin and (A-2) a polyester resin, (B) a styrene-based polymer, (C) an impact-reinforcing agent and (D) a phenol-based antioxidant.

Process of Producing Thermoplastic Starch/Polymer Blends

A process of producing a thermoplastic starch/polymer blend involves introducing dry starch into a twin-screw extruder at a first location along the extruder, introducing a plasticizer into the twin-screw extruder at a second location along the extruder downstream of the first location to form a starch paste and then gelatinizing the starch paste in the extruder to form thermoplastic starch, and, introducing dry polymer at ambient temperature into the twin-screw extruder at a third location along the extruder downstream of the second location to form a blend with the thermoplastic starch in the extruder.

Methods of Improving Polyethylene Stretch Films

Methods of improving polyethylene stretch film that include providing interpolymer resin particles, forming a polyethylene blend composition by blending from about 0.1 to about 10 percent by weight based on the weight of the blend composition of interpolymer resin particles into one or more polyethylene resins; and forming a film from the polyethylene blend composition. The interpolymer resin particles contain a styrenic polymer intercalated within a first polyolefin, where the first polyolefin is present at from about 20% to about 80% by weight based on the weight of the particles, and the styrenic polymer is present at from about 20% to about 80% by weight based on the weight of the particles.

Styrene resin composition, and molded article thereof

Provided are a styrene resin composition for use in electronic component packaging such as embossed carrier tape, a sheet which has a large drawing ratio (pocket depth) and in which pockets exhibiting superior transparency and strength and can be thermoformed, and a carrier tape which is thermoformed from the sheet and which allows the verification of letters and the like formed on packaged electronic components from outside the pockets. The electronic component packaging sheet includes: (A) 29-65 mass parts of a styrene-conjugated diene block copolymer; (B) 51-15 mass parts of a polystyrene resin; and (C) 20-9 mass parts of an impact resistant polystyrene resin. Components (A)-(C) each have a weight average molecular weight within a specified range.

Polyamide resin composition, expanded polyamide resin molding, and automotive resin molding

Provided is a polyamide resin composition which can provide an expanded molding being superior in heat resistance and sufficiently reduced in weight and having high load resistance by a simple molding process. The polyamide resin composition is characterized by comprising a polyamide resin (A), a glycidyl-group-containing styrene copolymer (B) having two or more glycidyl groups per molecule, a weight average molecular weight of 4000 to 25000 and an epoxy value of 400 to 2500 Eq/1×10 6 g and an inorganic reinforcing material (C) in a proportion such that the content of the glycidyl-group-containing styrene copolymer (B) is 0.2 to 25 parts by mass and the content of the inorganic reinforcing material (C) is 0 to 350 parts by mass relative to 100 parts by mass of the polyamide resin (A).

Rubber composition including a functionalized thermoplastic polymer

The present invention relates to a diene rubber composition reinforced with an inorganic filler comprising a thermoplastic polymer bearing, at at least one end, a silanol or silyl ether functional group. The presence of the functional thermoplastic polymer makes it possible to improve the compromise of performances, which are the handling and the grip, of a tyre having a tread that is based on such a composition.

Crosslinked polymer nanoparticles containing composition, method for preparing a copolymer using the composition, and vinyl chloride resin with improved foam molding properties

Disclosed is a crosslinked polymer nanoparticle containing composition, a method for preparing a copolymer using the composition, and a vinyl chloride resin with improved foam molding properties. Processing aid in according with the present invention, provides the effects of improved foam molding properties and processibility of a vinyl chloride resin, during a foam molding process upon being added to the vinyl chloride resin.

MULTIFUNCTIONAL BIOCOMPOSITE ADDITIVE COMPOSITIONS AND METHODS

Biocomposite compositions and compositions, which include dried distillers solubles, and which can be used in making biocomposite compositions are described. Methods for preparing the compositions are also described. 1. A extrudate comprising:a polymeric material in an amount of 60 to 99.5 weight percent; anddried distillers solubles in an amount of 0.5 to 20 weight percent, wherein the weight percents are based on a total weight of the extrudate.2. The extrudate of claim 1 , wherein the dried distillers solubles has a moisture content of 0.5 to 15 weight percent.3. The extrudate of claim 1 , further comprising a metal oxide in an amount of 0.025 to 8 weight percent and fiber in an amount of 0.025 to 8 weight percent.4. The extrudate of claim 3 , wherein the metal oxide is titanium oxide claim 3 , zinc oxide and mixtures thereof.5. The extrudate of claim 3 , further comprising latex in an amount of 0.005 to 6 weight percent.6. The extrudate of claim 5 , wherein the latex is acrylic late or styrenated acrylic latex.7. The extrudate of claim 1 , wherein the polymeric material is a thermoplastic claim 1 , thermoset claim 1 , and mixtures thereof.8. The extrudate of claim 7 , wherein the thermoplastic is selected from the group consisting of polyamides claim 7 , polyolefins claim 7 , polyvinyl chloride claim 7 , polyacrylate claim 7 , polyacetate claim 7 , polystyrene claim 7 , styrene acryloniteile claim 7 , and mixtures thereof.9. The extrudate of claim 7 , wherein the thermoplastic is selected from the group consisting of polyamides claim 7 , polyolefins claim 7 , polyvinyl chloride claim 7 , polyacrylate claim 7 , polyacetate claim 7 , polystyrene claim 7 , styrene acryloniteile claim 7 , and mixtures thereof.10. The extrudate of claim 7 , wherein the polymeric material is selected from the group consisting of a polylactic acid claim 7 , a polyhydroxyalkanoates claim 7 , a polyhydroxyvalerate claim 7 , a polyesteramide claim 7 , a polycaprolactone claim 7 , a ...

Thermally foamable resin composition, thermally foamable resin sheet, foam, and production method thereof

A thermally foamable resin composition includes a base resin, foamable resin particles, and a cross-linking agent, wherein each of the foamable resin particles contains a solid resin and a thermally expandable substance contained in the solid resin.

Terminated covered electric wire, wire harness, and anticorrosive agent

The object is to provide a terminated covered electric wire and a wire harness in which an anticorrosive agent comes into intimate contact with the surface of a terminal fitting and a high anticorrosive performance is exhibited in an electrical connection portion between an electric wire conductor and the terminal fitting even when oil adheres to the surface of the terminal fitting, and to provide an anticorrosive agent capable of exhibiting such a high anticorrosive performance. An electrical connection portion in which a terminal fitting having a surface to which processing oil adheres and an electric wire conductor of a covered electric wire are electrically connected to each other is covered with an anticorrosive agent containing an adhesive resin and an oil-adsorbing organic macromolecule to configure a terminated covered electric wire.

FIRE RETARDANT THERMOPLASTIC RESIN COMPOSITION AND ELECTRIC WIRE COMPRISING THE SAME (As Amended)

Disclosed are a fire retardant thermoplastic resin composition suitable for preparing an electric wire, etc. by enhancing extrudability of a resin composition without hindering fire retardancy of the resin composition, and an electric wire comprising the same. The fire retardant thermoplastic resin composition comprises a matrix resin that comprises 20 to 35% by weight of a poly arylene ether resin, 20 to 35% by weight of a vinyl aromatic resin and 5 to 20% by weight of an olefin-based resin comprising a rubber ingredient, 1 to 10% by weight of a room-temperature liquid-type fire retardant, and 8 to 20% by weight of an ancillary fire retardant, based on 100% by weight of a mixture of a poly arylene ether resin, a vinyl aromatic resin, an olefin-based resin, a room-temperature liquid-type fire retardant and an ancillary fire retardant.

AUTOMOBILE INTERIOR COMPONENT FORMED OF REINFORCED POLYPHENYLENE ETHER-BASED RESIN COMPOSITION

This disclosure is to provide an automobile interior component formed of a reinforced polyphenylene ether-based resin composition, which is excellent in both urethane adhesion and in appearance after molding, mechanical properties such as tensile strength, bending strength and the like, and resident molding stability; and further has sufficient molding fluidity. Provided is an automobile interior component formed of a reinforced polyphenylene ether-based resin composition, containing a polyphenylene ether (A) whereof the reduced viscosity (chloroform solvent, measured at 30° C.) in the molded product is 0.30 to 0.45 dl/g, a styrene resin (B) and a glass fiber (C), where the content of the component (A) is 10 to 30 mass %, the content of the component (B) is 40 to 85 mass %, and the content of the component (C) is 5 to 30 mass % with respect to 100 mass % in total of the components (A) to (C). 1. An automobile interior component formed of a reinforced polyphenylene ether-based resin composition , comprising: a polyphenylene ether (A) whereof the reduced viscosity in the molded product (chloroform solvent , measured at 30° C.) is 0.30 to 0.45 dl/g; a styrene-based resin (B); and a glass fiber (C) , whereinthe content of the component (A) is 10 to 30 mass %, the content of the component (B) is 40 to 85 mass %, and the content of the component (C) is 5 to 30 mass %, in 100 mass % in total of the components (A) to (C).2. The automobile interior component formed of the reinforced polyphenylene ether-based resin composition according to claim 1 , wherein the number of terminal OH groups of the polyphenylene ether of the component (A) in the molded product is 100 to 200 μmol/g.3. The automobile interior component formed of the reinforced polyphenylene ether-based resin composition according to claim 1 , wherein the component (C) is a glass fiber sized with a urethane sizing agent.4. The automobile interior component formed of the reinforced polyphenylene ether-based resin ...

Ink composition for organic light-emitting device and organic light-emitting device

There is provided an ink composition for an organic light-emitting device which can easily form a light-emitting layer having more excellent uniformity and which is suitable for forming a light-emitting layer by a wet method. The ink composition includes a light-emitting material, a binder resin, and a solvent, the binder resin containing a multi-branched copolymer of a monovinyl compound composed of a styrene-based monomer as an essential component with a multifunctional vinyl compound containing two or more ethylenically unsaturated double bonds, and the copolymer having a weight-average absolute molecular weight within a range of 200,000 to 800,000 determined by gel permeation chromatography using a multi-angle laser light scattering detector and a degree of branching within a range of 0.20 to 0.55 determined from an inertial radius. An organic light-emitting device includes a positive electrode; a light-emitting layer, and a negative electrode, the light-emitting layer containing the binder resin.

PROPYLENE BASED RESIN COMPOSITION AND USE THEREOF

Means for solving the problems 1. A thermoplastic resin composition (X2) comprising (A2) , (B2) , (C2) , (D2) , and (E2) below:5 to 95 wt % of a propylene/α-olefin copolymer (B2) whose melting point is not higher than 100° C. or not observed when measured with a differential scanning calorimeter (DSC);5 to 95 wt % of a styrene-based elastomer (C2);0 to 90 wt % of an isotactic polypropylene (A2);{'sup': '3', '0 to 70 wt % of an ethylene/α-olefin copolymer (D2) whose density is in the range of 0.850 to 0.910 g/cm,'}wherein the total of (A2), (B2), (C2), and (D2) is 100 wt %; anda softener (E2) in an amount of 0 to 400 parts by weight relative to 100 parts by weight of the total of (A2), (B2), (C2), and (D2).2. The thermoplastic resin composition (X2) according to claim 1 , wherein the propylene/α-olefin copolymer (B2) is a copolymer of propylene and at least one C-Cα-olefin.3. The thermoplastic resin composition (X2) according to claim 1 , wherein the propylene/α-olefin copolymer (B2) is a propylene/1-butene copolymer whose molecular weight distribution (Mw/Mn) is 3 or less as measured by gel permeation chromatography (GPC).4. The thermoplastic resin composition (X2) according to claim 1 , wherein the propylene/α-olefin copolymer (B2) is obtained by polymerization using a metallocene catalyst.5. A crosslinked product of the thermoplastic resin composition (X2) obtained by crosslinking the thermoplastic resin composition (X2) according to .6. A molded article made of the thermoplastic resin composition (X2) according to .7. A molded article made of the crosslinked product according to .8. A molded article made of a crosslinked product of the thermoplastic resin composition (X2) obtained by crosslinking the thermoplastic resin composition (X2) according to claim 5 , obtained by further crosslinking a molded article made of the thermoplastic resin composition (X2) according to . This application is a Divisional application of U.S. Ser. No. 13/619,135 filed Sep. 14, 2012; ...

POLYIMIDE PRECURSOR SOLUTION AND METHOD FOR PRODUCING POLYIMIDE FILM

A polyimide precursor solution includes a polyimide precursor, an aqueous solvent containing dimethyl sulfoxide and water, and particles. The content of the dimethyl sulfoxide relative to the particles is within a range of 0.15 to 2.00 in terms of mass ratio. 1. A polyimide precursor solution comprising:a polyimide precursor;an aqueous solvent containing dimethyl sulfoxide and water; andparticles,wherein a content of the dimethyl sulfoxide relative to the particles is within a range of 0.15 to 2.00 in terms of mass ratio.2. The polyimide precursor solution according to claim 1 , wherein a content of the water relative to the aqueous solvent is within a range of 60% by mass to 90% by mass.3. The polyimide precursor solution according to claim 1 , wherein the polyimide precursor solution contains the particles within a range of 40% by volume to 80% by volume relative to a total volume of a solid content of the polyimide precursor and the particles.4. The polyimide precursor solution according to claim 3 , wherein a content of the particles is within a range of 50% by volume to 70% by volume.5. The polyimide precursor solution according to claim 1 , wherein the content of the dimethyl sulfoxide relative to the water is within a range of 5% by mass to 20% by mass.6. The polyimide precursor solution according to claim 1 , wherein the aqueous solvent contains an organic amine compound.7. The polyimide precursor solution according to claim 6 , wherein the organic amine compound selected from the group consisting of triethylamine claim 6 , N-alkylpiperidine claim 6 , 2-dimethylaminoethanol claim 6 , and a tertiary cyclic amine compound.8. The polyimide precursor solution according to claim 7 , wherein the tertiary cyclic amine compound is a morpholine compound.9. The polyimide precursor solution according to claim 8 , wherein the morpholine compound is N-methylmorpholine.10. The polyimide precursor solution according to claim 1 , wherein the particles are resin particles.11 ...

SLURRY COMPOSITION FOR NON-AQUEOUS SECONDARY BATTERY FUNCTIONAL LAYER, SEPARATOR FOR NON-AQUEOUS SECONDARY BATTERY, AND NON-AQUEOUS SECONDARY BATTERY

Provided is a slurry composition for a non-aqueous secondary battery functional layer with which it is possible to form a functional layer that has excellent adhesiveness after immersion in electrolyte solution and can cause a secondary battery to display excellent rate characteristics and cycle characteristics while, on the other hand, reducing the amount of gas remaining inside the secondary battery. The slurry composition contains a particulate polymer and a solvent. The particulate polymer has a core-shell structure including a core portion and a shell portion at least partially covering an outer surface of the core portion. The particulate polymer has a glass-transition temperature of 20° C. or higher and has a surface acid content of not less than 0.05 mmol/g and not more than 0.50 mmol/g.

FLAME-RETARDANT RESIN COMPOSITION AND FLAME-RETARDANT RESIN MOLDED ARTICLE

To improve the thermal stability of a brominated polymer type flame retardant in a flame-retardant resin composition containing a styrene-based resin and the brominated polymer type flame retardant to provide a flame-retardant resin molded article in which occurrences of black foreign substances and discoloration decrease. The flame-retardant resin composition contains a styrene-based resin, a brominated polymer type flame retardant, an epoxy compound, and a halogen capture agent, wherein a content of bromine is 18 to 42% by mass. 19-. (canceled)10. A flame-retardant resin composition characterized by comprising:a styrene-based resin;a brominated polymer type flame retardant;an epoxy compound; anda halogen capture agent,wherein a content of bromine is 18 to 42% by mass.11. The flame-retardant resin composition according to claim 10 ,wherein the flame-retardant resin composition contains 4 to 25 parts by mass of the epoxy compound and 0.8 to 15 parts by mass of the halogen capture agent based on a total of 100 parts by mass of the styrene-based resin and brominated polymer type flame retardant.12. The flame-retardant resin composition according to claim 10 , wherein the halogen capture agent contains at least a dolomite-based compound and a hydrotalcite-based compound.13. The flame-retardant resin composition according to claim 11 , wherein the halogen capture agent contains at least a dolomite-based compound and a hydrotalcite-based compound.14. The flame-retardant resin composition according to claim 12 , wherein a mass ratio of the dolomite-based compound to the hydrotalcite-based compound (dolomite-based compound/hydrotalcite-based compound) is 10/90 to 90/10.15. The flame-retardant resin composition according to claim 13 , wherein a mass ratio of the dolomite-based compound to the hydrotalcite-based compound (dolomite-based compound/hydrotalcite-based compound) is 10/90 to 90/10.16. The flame-retardant resin composition according to claim 10 , characterized by ...

AQUEOUS COLD SEAL ADHESIVE

Described is an aqueous cold seal adhesive in the form of an aqueous polymer dispersion comprising a mixture of a first polymer and a second polymer, wherein the first polymer is an emulsion polymer prepared in the presence of a protective colloid and is composed to an extent of at least 60% by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates and has a glass transition temperature of less than 0° C.; and wherein the second polymer is an emulsion polymer prepared in the presence of a protective colloid and is composed to an extent of at least 60% by weight of principal monomers selected from the group consisting of vinylaromatics having up to 20 C atom, and has a glass transition temperature of at least 50° C. Also described are cold sealable coated polymer films coated with the aqueous cold seal adhesive and a method for producing a cold-sealed pack by applying the aqueous cold seal adhesive to a packaging substrate. 1. An aqueous cold seal adhesive in the form of an aqueous polymer dispersion comprising a mixture of at least one first polymer and at least one second polymer ,wherein the first polymer is an emulsion polymer comprising, to an extent of at least 60% by weight, one or more principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, the first polymer being prepared by emulsion polymerization of free-radically polymerizable monomers in the presence of at least one protective colloid, and the first polymer having a glass transition temperature of less than 0° C.;wherein the second polymer is an emulsion polymer comprising, to an extent of at least 60% by weight, one or more principal monomers selected from the group consisting of vinylaromatics having up to 20 C atoms, the second polymer being prepared by emulsion polymerization of free-radically polymerizable monomers in the presence of at least one protective colloid, and the second polymer having a glass transition ...

SOLVENT COMPOSITION AND PRODUCTION METHOD THEREFOR

A solvent composition includes an organic solvent including one or more organic solvents (A) and one or more organic solvents (B), and one or more types of core-shell polymer particles each comprising a core layer and a shell layer. The organic sol vents (A) have a polar teen δp of a Hansen solubility parameter of less than 11 and a hydrogen bond term δh of less than 10, and the organic solvents (B) satisfy at least one of 11 or more of the polar term δp or 10 or more of the hydrogen bond term δh. A weight ratio of (A) to (B) ranges from 15:85 to 95:5. Based on a total weight of the solvent composition, a content of the core-shell polymer particles is 20 to 40% by weight and a water content is 1% by weight or less. 1. A solvent composition comprising:an organic solvent comprising one or more organic solvents (A) and one or more organic sol vents (B); andone or more types of core-shell polymer particles each comprising a core layer and a shell layer,wherein the one or more organic solvents (A) have a polar term δp of a Hansen solubility parameter of less than 11 and a hydrogen bond term δh of less than 10,wherein the one or more organic solvents (B) satisfy at least one of: 11 or more of the polar δp; or 10 or more of the hydrogen bond term δh,wherein a weight ratio of the one or more organic solvents (A) to the one or more organic solvents (B) ranges from 15:85 to 95:5, andwherein, based on a total weight of the solvent composition, a content of the core-shell polymer particles is 20 to 40% by weight and a water content is 1% by weight or less.2. The solvent composition according to claim 1 , whereinthe organic solvent (A) is one or more solvents selected from the group consisting of toluene, xylene, ethyl acetate, propylene glycol monomethyl ether acetate, acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone, andthe organic solvent (B) is one or more solvents selected from the group consisting of butanol, methyl cellosolve, butyl cellosolve, ...

Pneumatic tire

The present invention provides a pneumatic tire achieving a balanced improvement in fuel economy, abrasion resistance, and wet grip performance. The present invention relates to a pneumatic tire, including a tread containing a tread rubber composition, the tread rubber composition containing a rubber component including 30% by mass or more of a styrene-butadiene rubber, the tread rubber composition containing, per 100 parts by mass of the rubber component: 80 to 150 parts by mass of silica; 0.1 to 3.0 parts by mass of a tetrazine compound of formula (1); and 50 parts by mass or less of a hydrocarbon resin having a SP value of 7.5 to 10.5, the styrene-butadiene rubber having a styrene content of 23% by mass or higher.

AQUEOUS POLYMER DISPERSIONS FOR ADHESIVES

The present invention relates to aqueous polymer dispersions having a polymer content of at least 55% by weight that are suitable for pressure sensitive adhesives. The invention also relates to a process for preparing these aqueous polymer dispersions and also to the use of the aqueous polymer dispersions in pressure sensitive adhesives and, respectively, pressure sensitive adhesive compositions, especially in pressure sensitive adhesives for transparent substrates, such as plastics labels. The aqueous polymer dispersions have a polymer content of at least 55% by weight, based on the total weight of the dispersion, the polymer being composed of ethylenically unsaturated monomers M and having a glass transition temperature below −10° C., in which the dispersed polymer particles have a polymodal particle size distribution, in which at least 70% by weight have a particle diameter of below 350 nm. 2. The process according to claim 1 , the seed polymer being added when 10% to 60% by weight of the monomers to be polymerized are located in the polymerization reactor.3. The process according to claim 1 , the seed polymer 1 being used in an amount of 0.1% to 2% by weight claim 1 , based on the monomers to be polymerized.4. The process according to claim 1 , the seed polymer 1 having a weight-average particle size in the range from 10 to 150 nm.5. The process according to claim 1 , the seed polymer 2 being used in an amount of 0.05% to 2% by weight claim 1 , based on the monomers to be polymerized.6. The process according to claim 1 , wherein seed polymer 1 and seed polymer 2 comprise vinylaromatic monomers.7. The process according to claim 1 , wherein seed polymer 1 and seed polymer 2 comprise styrene.8. The process according to claim 1 , wherein seed polymer 1 and seed polymer 2 comprise C-Calkyl acrylates and/or C-Calkyl methacrylates.9. The process according to claim 1 , wherein seed polymer 1 and seed polymer 2 comprise butyl acrylate and methyl methacrylate. This ...

ACRYLIC RUBBER COMPOSITION

An acrylic rubber composition comprising 5 to 80 parts by weight, preferably 10 to 60 parts by weight, more preferably 20 to 40 parts by weight, of a styrene-based resin, based on 100 parts by weight of acrylic rubber. A vibration insulation member having an excellent tan δ value at a high temperature and improved vibration insulation properties can be molded by adding a specific ratio of a styrene-based resin to acrylic rubber. This acrylic rubber composition can be effectively used as a molding material for a mount, a grommet, or the like in the vicinity of an automobile engine used in a high temperature environment. 1. An acrylic rubber composition comprising 5 to 80 parts by weight of a styrene-based resin , based on 100 parts by weight of acrylic rubber.2. A vibration insulation member obtained by vulcanizing molding of the acrylic rubber composition according to .3. The vibration insulation member according to claim 2 , which is used as a mount or a grommet in the vicinity of an automobile engine. The present invention relates to an acrylic rubber composition. More particularly, the present invention relates to an acrylic rubber composition that can form a member having excellent vibration insulation properties at a high temperature.Conventional rubber materials have a tendency that tan δ is likely to decrease at a high temperature and vibration insulation effects are impaired. Acrylic rubber is used as a molding material of a vibration insulation member for a mount, a grommet, or the like in the vicinity of an automobile engine used in a high temperature environment; however, the same tendency is also observed in this case. There is a demand for improving this tendency.Patent Document 1: JP-A-11-158343An object of the present invention is to provide an acrylic rubber composition that is effectively used, for example, as a molding material of a vibration insulation member having a high tan δ value at a high temperature and excellent vibration insulation ...

COMPOSITION FOR PATTERN FORMATION, AND PATTERN-FORMING METHOD

A composition for pattern formation includes a first polymer, a second polymer and a solvent. The first polymer includes: a first block including a first structural unit derived from a substituted or unsubstituted styrene; and a second block including a second structural unit other than the first structural unit. The second polymer includes: the first structural unit; and a group bonding to at least one end of a main chain thereof and including a polar group. The polar group is preferably a hydroxy group or a carboxyl group. A number average molecular weight of the second polymer is preferably no greater than 6,000. A mass ratio of the second polymer to the first polymer is preferably no less than 0.15 and no greater than 0.4. The solvent preferably comprises a compound comprising a hydroxyl group and an alkyl ester group. 1. A composition for pattern formation comprising:a first polymer comprising: a first block comprising a first structural unit derived from a substituted or unsubstituted styrene; and a second block comprising a second structural unit other than the first structural unit;a second polymer comprising: the first structural unit; and a group bonding to at least one end of a main chain thereof and comprising a polar group; anda solvent.2. The composition according to claim 1 , wherein the polar group is a hydroxy group or a carboxyl group.3. The composition according to claim 1 , wherein a number average molecular weight of the second polymer is no greater than 6 claim 1 ,000.4. The composition according to claim 1 , wherein a mass ratio of the second polymer to the first polymer is no less than 0.15 and no greater than 0.4.5. The composition according to claim 1 , wherein the solvent comprises a compound comprising a hydroxyl group and an alkyl ester group.6. The composition according to claim 5 , wherein a content of the compound in the solvent is no less than 20% by mass and no greater than 50% by mass.7. The composition according to claim 1 , ...

Extruded styrene resin foam and process for producing same

An extruded styrenic resin foam may include 100 parts by weight of a styrenic resin; 0.5 to 8.0 parts by weight of a flame retardant; 1.0 to 5.0 parts by weight of graphite; a saturated hydrocarbon having 3 to 5 carbon atoms; and a hydrofluoroolefin. 1 kg of the extruded styrenic resin foam includes the hydrofluoroolefin in an amount of 0.05 to 0.40 mol, and the saturated hydrocarbon in an amount of 0.10 to 0.40 mol, a total amount of the saturated hydrocarbon and the hydrofluoroolefin being 0.30 to 0.50 mol relative to 1 kg of the extruded styrenic resin foam.

Molded Product Having Fabric Texture

A molded product according to the present invention is a molded product having a structure in which colored particles are dispersed in thermoplastic resin, wherein the colored particles have an average particle size of about 250-3,200 μm as measured by a particle size analyzer, and are included in an amount of about 0.05-5 parts by weight with respect to about 100 parts by weight of the thermoplastic resin, a three-dimensional pattern is formed on at least one surface of the molded product, and the three-dimensional pattern has a 10-point average roughness (Rz) of about 50-500 μm and a number of different brightness values of about 30-60. The molded product has excellent impact resistance, excellent heat resistance, and the like, and has an appearance similar to actual fabric. 1. A molded product having a structure in which colored particles are dispersed in a thermoplastic resin , the molded article having a three-dimensional pattern formed on at least one surface thereof ,wherein the colored particles have an average particle diameter of about 250 μm to about 3,200 μm, as measured using a particle size analyzer, and are present in an amount of about 0.05 parts by weight to about 5 parts by weight relative to about 100 parts by weight of the thermoplastic resin, andthe three-dimensional pattern having a ten-point average roughness (Rz) of about 50 μm to about 500 μm and about 30 to about 60 different brightness values, the number of different brightness values being calculated by scanning a 3 mm×3 mm area of the three-dimensional pattern at a resolution of 600 dpi, converting the scanned image into an image represented by 4,900 pixels, and measuring brightness (L*) of each pixel using the CIE 1976 L*a*b* (CIELAB) color system.2. The molded product according to claim 1 , wherein the thermoplastic resin comprises a polycarbonate resin and/or a rubber-modified aromatic vinyl copolymer resin.3. The molded product according to claim 2 , wherein the rubber-modified ...

Poly(vinylbiphenyl) and Poly(vinylcyclohexylstyrene) Polymers and Articles Therefrom

Disclosed is an article comprising polymers and copolymers selected from the group consisting of poly(vinylbiphenyl), poly(vinylcyclohexylstyrene), substituted versions thereof, and blends thereof, the polymer or copolymer having a weight average molecular weight (Mw) of at least 100 kg/mole and a glass transition temperature (Tg) of at least 100° C. The polymers are desirably processed in the melted state at a temperature of at least 150° C. to impart orientation and extensional strain hardening. 1. An article comprising polymers selected from the group consisting of poly(vinylbiphenyl) , poly(vinylcyclohexylstyrene) , substituted versions thereof , and blends thereof , the polymer having a weight average molecular weight (Mw) of at least 100 kg/mole and a glass transition temperature (Tg) of at least 100° C. , wherein the polymer or polymer blend exhibits extensional strain hardening at a temperature of at least 150° C.2. The article of claim 1 , wherein the polymer or polymer blend has a flexural modulus of at least 2000 MPa.3. The article of claim 1 , wherein the polymer or polymer blend has a Tg within a range from 100° C. to 200° C.4. The article of claim 1 , wherein the PVBP or PCHS polymer has an Mw within a range from 100 kg/mole to 1000 kg/mole.5. The article of claim 1 , wherein the PVBP or PCHS polymer has an Mw/Mn value within the range from 1.5 to 5.6. The article of claim 1 , also comprising poly(phenylene oxide) claim 1 , a diene elastomer claim 1 , or a combination of the two.7. The article of claim 1 , wherein poly(vinylbiphenyl) claim 1 , poly(vinylcyclohexylstyrene) are copolymers comprising within a range from 0.01 to 5 wt % divinylbenzene.8. The article of claim 1 , wherein the polymer or polymer blend exhibits extensional strain hardening at a temperature of at least 170° C.9. The article of claim 1 , wherein the polymer or polymer blend exhibits an increase in the viscosity above the LVE over time of at least 100 MPa·sec at a given scan rate. ...

AQUEOUS BINDER FORMULATION

Aqueous binder formulation comprising a copolymer having a glass transition temperature 80° C., a polyol compound and a phosphorus compound. 1: An aqueous binder formulation , comprising:a) a copolymer A, comprising, in polymerized form,{'sub': 3', '6, '≥20% and ≤50% by weight of at least one α,β-monoethylenically unsaturated C- to C-monocarboxylic acid (A1) and'}≥50% and ≤80% by weight of at least one other monoethylenically unsaturated compound (A2),wherein a total amount of A1 and A2 is 100% by weight,the copolymer A has a weight-average molecular weight in a range of from ≥5000 to ≤20 000 g/mol,the copolymer A has a glass transition temperature Tg in a range of ≥80° C., measured according to DIN EN ISO 11357-2 (2013-09), and≥70 mol % of carboxyl groups present in the copolymer A have been neutralized with a volatile base;b) an organic compound which comprises at least 2 hydroxyl groups (polyol B), wherein an amount of the polyol B is determined such that a molar ratio of carboxyl groups present in the copolymer A to hydroxyl groups present in the polyol B is in a range of from 10:1 to 1:1; andc) a phosphorus-containing compound (phosphorus compound C), wherein an amount of the phosphorous compound is ≥3% and ≤20% by weight based on an amount of A1 present in the copolymer A in polymerized form.2: The aqueous binder formulation of claim 1 , wherein the copolymer A comprises claim 1 , in polymerized form claim 1 , as A2;≥50% and ≤80% by weight of at least one monoethylenically unsaturated aromatic compound (A2-1) and≥0% and ≤40% by weight of at least one other monoethylenically unsaturated compound distinct from A1 and A2-1,wherein a total amount of A2-1 and A2-2 is not more than 80% by weight of the total amount of A1 and A2.3: The aqueous binder formulation of claim 1 , wherein the copolymer A comprises claim 1 , in polymerized form claim 1 , acrylic acid and/or methacrylic acid as A1 and claim 1 , as A2 claim 1 , styrene and/or α-methylstyrene (A2-1) and methyl ...

Image display device sealing material and image display device sealing sheet

The image display device sealing material contains a resin component and a curing agent, wherein the resin component contains biphenyl skeleton-containing epoxy resin having a weight-average molecular weight of 200 or more and 100,000 or less, alicyclic skeleton-containing epoxy resin having a weight-average molecular weight of 180 or more and 790 or less, and styrene oligomer having a weight-average molecular weight of 750 or more and 4000 or less.

HEAT-RESISTANT SILANE CROSSLINKED RESIN MOLDED BODY AND METHOD OF PRODUCING THE SAME, HEAT-RESISTANT SILANE CROSSLINKABLE RESIN COMPOSITION AND METHOD OF PRODUCING THE SAME, SILANE MASTER BATCH, AND HEAT-RESISTANT PRODUCT USING HEAT-RESISTANT SILANE CROSSLINKED RESIN MOLDED BODY

A method comprising at least (a) a step of preparing a silane master batch by melt-kneading, to 100 parts by mass of a base resin (R) containing a non-aromatic organic oil and ethylene rubber, an organic peroxide of from 0.01 to 0.6 parts by mass, an inorganic filler of from 10 to 400 parts by mass, and a silane coupling agent of from 1 to 15.0 parts by mass, at a temperature equal to or higher than the decomposition temperature of the organic peroxide; a heat-resistant silane crosslinked resin molded body and a heat-resistant silane crosslinkable resin composition prepared by the method, and a silane master batch and a heat-resistant product. 1. A method of producing a heat-resistant silane crosslinked resin molded body , comprising:{'sub': 'B', '(a) a step of preparing a silane master batch by melt-kneading, to 100 parts by mass of a base resin (R) containing a non-aromatic organic oil and ethylene rubber, an organic peroxide of from 0.01 to 0.6 parts by mass, an inorganic filler of from 10 to 400 parts by mass, and a silane coupling agent of from 1 to 15.0 parts by mass, at a temperature equal to or higher than the decomposition temperature of the organic peroxide,'}(b) a step of obtaining a mixture by mixing the silane master batch and a silanol condensation catalyst,(c) a step of obtaining a molded body by molding the mixture, and(d) a step of obtaining a heat-resistant silane crosslinked resin molded body by contacting the molded body with water.2. The method of producing a heat-resistant silane crosslinked resin molded body according to claim 1 , wherein the base resin (R) comprises a styrene-based elastomer.3. The method of producing a heat-resistant silane crosslinked resin molded body according to claim 1 , wherein the mixing amount of the silane coupling agent is more than 4 parts by mass and 15.0 parts by mass or less claim 1 , with respect to 100 parts by mass of the base resin (R).4. The method of producing a heat-resistant silane crosslinked resin ...

POLYSTYRENE-CONTAINING COMPOSITE RESIN PARTICLES AND METHOD FOR PRODUCING SAME, EXPANDABLE COMPOSITE RESIN PARTICLES, PRE-EXPANDED PARTICLES, AND EXPANDED MOLDED ARTICLE

Polystyrene-based composite resin particles includes 100 to 500 parts by weight of a polystyrene-based resin with respect to 100 parts by weight of an ethylene-vinyl acetate copolymer resin. The polystyrene-based composite resin particles are impregnated with a volatile blowing agent and are pre-expanded to obtain pre-expanded particles; the obtained pre-expanded particles are immersed in tetrahydrofuran for 24 hours to obtain an extract A; and the pre-expanded particles are divided into two halves through the center to prepare halved particles, and the halved particles are immersed in tetrahydrofuran for 24 hours to obtain an extract B; and the obtained extract A and extract B are subjected to a GPC (gel permeation chromatography) measurement and obtain the following results: the polystyrene-based resin having a weight-average molecular weight (Mw) of 100,000 to 500,000 gives a peak obtained from chromatograms for the extract A and for the extract B.

Resin Composition, Prepreg, Metal Foil-Clad Laminate, Resin Sheet, and Printed Wiring Board

Provided are a resin composition that can form a printed wiring board with a low dielectric constant and dielectric loss tangent and excellent alkali resistance and desmear resistance; and a prepreg, a resin sheet, a metal foil-clad laminate, and a printed wiring board formed using this resin composition. The resin composition contains a styrene-based elastomer (A), a styrene oligomer (B), a maleimide compound (C), and a cyanate ester compound (D).

Tire Tread Rubber Composition

Disclosed herein are tire tread rubber compositions comprising a specified elastomer component, reinforcing silica filler, a specified hydrocarbon resin, a cure package, and optionally oil. The elastomer component includes styrene-butadiene rubber; polybutadiene; and natural rubber, polyisoprene, or a combination thereof. 119-. (canceled)20. A tire tread rubber composition comprising: i. 10-50 parts of natural rubber, polyisoprene, or a combination thereof, and', 'ii. 10-60 parts of polybutadiene rubber having a cis bond content of at least 95% and a Tg of less than −101° C.,, 'a. 100 parts of an elastomer component comprising'}wherein the total amount of (i) and (ii) is at least 50 phr,b. at least one reinforcing silica filler in an amount of 61-150 phr,c. at least one hydrocarbon resin in an amount of 21-50 phr, wherein the resin has a Tg of about 30 to about 50° C.,d. no more than 30 phr of oil, ande. a cure package,wherein the total amount of (c) and (d) is no more than 59 phr.21. The tire tread rubber composition of claim 20 , wherein the elastomer component further comprises 20-50 parts of at least one styrene-butadiene rubber.22. The tire tread rubber composition of claim 20 , wherein the elastomer component further comprises 20-45 parts of at least one styrene-butadiene rubber and the amount of hydrocarbon resin is no more than 45 phr.23. The tire tread rubber composition of claim 20 , comprising no more than 20 phr of carbon black filler.24. A tire tread rubber composition comprising: i. 20-45 parts of natural rubber, polyisoprene, or a combination thereof,', 'ii. 10-60 parts of polybutadiene rubber having a cis bond content of at least 95% and a Tg of less than −101° C., and', 'iii. 20-45 parts of at least one styrene-butadiene rubber,, 'a. 100 parts of an elastomer component comprising'}wherein the total amount of (i) and (ii) is at least 55 phr,b. at least one reinforcing silica filler in an amount of 81-120 phr and no more than 20 phr of carbon black ...

Process for making an organic charge transporting film

A single liquid phase formulation useful for producing an organic charge transporting film. The formulation contains: (a) a polymer resin having M w at least 3,000 and having arylmethoxy linkages; (b) an acid catalyst which is an organic Bronsted acid with pKa≤4; a Lewis acid comprising a positive aromatic ion and an anion which is (i) a tetraaryl borate having the formula (I) wherein R represents zero to five non-hydrogen substituents selected from D, F and CF 3 , (ii) BF 4 − , (iii) PF 6 − , (iv) SbF 6 − , (v) AsF 6 − or (vi) ClO 4 − ; or a thermal acid generator.

WINDING CORE AND WINDING CORE MANUFACTURING METHOD

The present invention provides a winding core which is lightweight, and which has an excellent dimensional accuracy and deflection reducing property in a long length product. Provided is a winding core obtained by molding a resin composition comprising: at least one type of amorphous resin (A) selected from a styrene resin, a polycarbonate, a polyarylate, a polyphenylene oxide and a polysulfone; a polylactic acid (B); and an inorganic filler; wherein the resin composition includes: from 50 to 80 parts by mass of the amorphous resin (A), and from 20 to 50 parts by mass of the polylactic acid resin (B) (wherein the total amount of the amorphous resin (A) and the polylactic acid (B) is 100 parts by mass). Preferably, the winding core further includes from 10 to 40 parts by mass of the inorganic filler (C). 1. A winding core obtained by molding a resin composition comprising: at least one type of amorphous resin (A) selected from a styrene resin , a polycarbonate , a polyarylate , a polyphenylene oxide and a polysulfone; a polylactic acid (B); and an inorganic filler (C);wherein the resin composition comprises: from 50 to 80 parts by mass of the amorphous resin (A), from 20 to 50 parts by mass of the polylactic acid resin (B), and from 10 to 40 parts by mass of the inorganic filler (C) (wherein the total amount of the amorphous resin (A) and the polylactic acid (B) is 100 parts by mass).2. The winding core according to claim 1 , wherein the inorganic filler (C) comprises talc.3. The winding core according to claim 1 , wherein the ratio of length [L] to inner diameter [D] (length [L]/inner diameter [D]) of the winding core is 2 or more.4. A winding core obtained by molding a resin composition comprising: at least one type of amorphous resin (A) selected from a styrene resin claim 1 , a polycarbonate claim 1 , a polyarylate claim 1 , a polyphenylene oxide and a polysulfone; a polylactic acid (B); and an inorganic filler (C);wherein the ratio of length [L] to inner ...

ANTIMICROBIAL COATING COMPOSITION WITH IMPROVED YELLOWING RESISTANCE

The present invention provides an antimicrobial coating composition comprising (i) a binder dispersion of (co)polymer particles and (ii) from 50 ppm to 2000 ppm, by dry weight based on total dry weight of the coating composition, a silver; wherein the binder dispersion comprises, as polymerized units, by dry weight based on total dry weight of the binder dispersion, (a) from 40% to 99.9% ethylenically unsaturated nonionic monomers and (b) from 0.1% to 60% phosphate group-containing (meth)acrylate monomers. 1. An antimicrobial coating composition comprising (i) a binder dispersion of (co)polymer particles and (ii) from 50 ppm to 2000 ppm , by dry weight based on total dry weight of the coating composition , a silver; wherein the binder dispersion comprises , as polymerized units , by dry weight based on total dry weight of the binder dispersion , (a) from 40% to 99.9% ethylenically unsaturated nonionic monomers and (b) from 0.1% to 60% phosphate group-containing (meth)acrylate monomers.2. The antimicrobial coating composition according to wherein the silver content is from 100 ppm to 1000 ppm claim 1 , by dry weight based on total dry weight of the coating composition.3. The antimicrobial coating composition according to wherein the mole ratio of the phosphate groups in the phosphate group-containing (meth)acrylate monomers to the silver is from 0.1 to 70.4. The antimicrobial coating composition according to wherein the (co)polymer particles have a molecular weight of from 400 to 500 claim 1 ,000 Dalton.5. The antimicrobial coating composition according to wherein the ethylenically unsaturated nonionic monomer is selected from styrene claim 1 , C-Calkyl esters of (methyl) acrylic acids claim 1 , derivatives thereof claim 1 , and any combinations thereof.6. The antimicrobial coating composition according to wherein the phosphate group-containing (meth)acrylate monomers are selected from mono- or di-ester of phosphoalkyl (meth)acrylates.7. The antimicrobial coating ...

Rubber composition for vulcanizing bladder and vulcanizing bladder

The present invention is to provide a rubber composition for vulcanizing bladder excellent in thermal conductivity and a vulcanizing bladder formed of the rubber composition, with which vulcanization efficiency can be improved. The rubber composition for vulcanizing bladder comprises, based on 100 parts by mass of a rubber component comprising 80% by mass or more of a butyl rubber, 20 to 200 parts by mass of at least one type of metal filler selected from the group consisting of metal powder, metal oxide powder, metal hydroxide powder and metal nitride powder, said metal filler having a Mohs hardness of 8 or lower and a mean particle size of 0.3 to 50 μm, and 20 to 80 parts by mass of a carbon black. The vulcanizing bladder is formed of the rubber composition for vulcanizing bladder.

POROUS THERMALLY INSULATING COMPOSITIONS CONTAINING HOLLOW SILICA PARTICLES

A thermally insulating composition comprising hollow spherical silica particles and a coating of a material having a thermal conductivity of less than 0.3 W/m·K on surfaces of said silica particles. In particular embodiments, the low conductivity coating material may be a polymer, such as polystyrene or polyvinylpyrrolidone, or the low conductivity coating material may be a quaternary ammonium salt of the Formula (1), i.e., RRRRNA, with at least one of R, R, R, and Rbeing an alkyl group containing at least ten carbon atoms (and Ais a counter anion), or the low conductivity coating material may be phenyl-C61-butyric acid methyl ester covalently bound to the hollow spherical silica particles. Also described herein is a method of thermally insulating a surface by applying a coating of the thermally insulating composition, described above, onto the surface. 2. The insulating composition of claim 1 , wherein said coating is polystyrene.3. The insulating composition of claim 1 , wherein said coating is polyvinylpyrrolidone.4. The insulating composition of claim 1 , wherein said coating is said quaternary ammonium salt having the formula (1).5. The insulating composition of claim 4 , wherein said quaternary ammonium salt contains a cetyltrimethylammonium portion.6. The insulating composition of claim 1 , wherein said coating is phenyl-C61-butyric acid methyl ester that is covalently bound by an amide bond claim 1 , in place of the ester group claim 1 , via a linker to the surface of the hollow spherical silica particles.7. The insulating composition of claim 1 , wherein said hollow spherical silica particles have a mean particle size of up to 1000 nm.8. The insulating composition of claim 1 , wherein said hollow spherical silica particles have a mean particle size of up to 500 nm.9. The insulating composition of claim 1 , wherein said hollow spherical silica particles do not contain surface porosity.10. The insulating composition of claim 1 , wherein said hollow spherical ...

THERMOPLASTIC RESIN COMPOSITION, METHOD FOR PRODUCING SAME AND MOLDED BODY

Disclosed is a thermoplastic resin composition designed to, even when containing a filler, reduce a trade-off between stiffness and impact resistance to achieve a balance between impact resistance and stiffness, a method for producing the same, and a molded body. The thermoplastic resin composition is obtained by blending a polyolefin resin, a polyamide resin containing an inorganic filler, and a modified elastomer having a reactive group that reacts with the polyamide resin, wherein the polyolefin resin has a number-average molecular weight of 350,000 or more, and the polyamide resin has a structure in which a hydrocarbon group interposed between adjacent amide bonds in a main chain has 5 or less straight chain carbon atoms. The molded body is composed of the thermoplastic resin composition. The method for producing the thermoplastic resin composition includes the step of melt-kneading a polyolefin resin and a melt-kneaded product of a polyamide resin and a modified elastomer. 1. A thermoplastic resin composition obtained by blending a polyolefin resin , a polyamide resin containing an inorganic filler , and a modified elastomer having a reactive group that reacts with the polyamide resin , whereinthe polyolefin resin has a number-average molecular weight of 350,000 or more, andthe polyamide resin has a structure in which a hydrocarbon group interposed between adjacent amide bonds in a main chain has 5 or less straight chain carbon atoms.2. A thermoplastic resin composition comprising a polyolefin resin , a polyamide resin containing an inorganic filler , and a modified elastomer having a reactive group that reacts with the polyamide resin , whereinthe polyolefin resin has a number-average molecular weight of 350,000 or more, andthe polyamide resin has a structure in which a hydrocarbon group interposed between adjacent amide bonds in a main chain has 5 or less straight chain carbon atoms.3. The thermoplastic resin composition according to claim 1 , whereinthe ...

COMPOSITION FOR RESIDUAL SANITIZATION

A composition for providing a residual sanitizing effect to a surface. The composition comprises a neutralized acrylic polymer, a neutralized acrylic resin or a combination thereof in combination, a biocidal active, and a carrier. The composition comprises a neutralized styrene acrylic polymer, a neutralized styrene acrylic resin or a combination thereof in combination, a biocidal active, and a carrier. 1. A composition for residual sanitization comprising:a neutralized acrylic polymer, a neutralized acrylic resin, or a combination thereof,a biocidal active, anda carrier.2. The composition according to claim 1 , wherein the biocidal active is a quaternary amine or a mixture of quaternary amines.3. The composition according to claim 1 , wherein the biocidal active is polyhexamethylene biguanide (PHMB).4. The composition according to claim 1 , wherein the biocidal active is a silanated quaternary amine or a mixture of silanated quaternary amines.5. The composition according to claim 1 , wherein the biocidal active is present in an amount from about 0.05 weight % to 2 weight %.6. The composition according to claim 1 , wherein the carrier is water.7. The composition according to claim 1 , wherein the neutralized acrylic polymer is a neutralized styrene acrylic polymer.8. The composition according to claim 1 , wherein the neutralized acrylic resin is a neutralized styrene acrylic resin.9. The composition according to claim 8 , wherein the neutralized styrene acrylic resin has a molecular weight (wt. av.) in a range of about 2 claim 8 ,000 to 18 claim 8 ,000.10. The composition according to claim 9 , wherein the neutralized styrene acrylic resin has a molecular weight (wt. av.) in a range of about 3 claim 9 ,000 to 10 claim 9 ,000.11. The composition according to claim 8 , wherein the neutralized styrene acrylic resin has a glass transition temperature Tg (DSC) in a range of about 100° C. to 120° C.12. The composition according to claim 8 , wherein the neutralized styrene ...

Hydroxyl group-containing methylstyrene and polymers incorporating same

Vulcanizates with desirable properties can be obtained from compounds incorporating polymers that include hydroxyl group-containing α-methylstyrene functionalities. The functionalities can be incorporated by using any or all of appropriate initiators, monomers and optional terminating compounds. Such polymers exhibit excellent interactivity with both conventional and non-conventional fillers.

THERMOPLASTIC STARCH COMPOSITION DERIVATIVES FROM AGRICULTURAL BYPRODUCTS

A thermoplastic starch composition acquired from compounding a mixture comprising starch-containing agricultural byproducts in 45 to 70% by weight of total composition, the agricultural byproducts having a starch content less than 50% dry weight; thermoplastic synthetic polymer in 25 to 50% by weight of total composition; plasticizer in 1 to 10% by weight of total composition; and coupling agent in 1 to 5% by weight of total composition; the compounding performed at a first temperature which is higher than room temperature. 125-. (canceled)26. A method for forming a bio-resin , said method comprising:forming a first blend by combining an agricultural byproduct having a starch content of less than 50% by dry weight and a plasticizer;forming a second blend by combining a synthetic polymer and a coupling agent; andcompounding the first blend and the second blend to form a bio-resin.27. The method of claim 26 , wherein the compounding includes combining and coextruding the first blend and second blend.28. The method of claim 26 , wherein the compounding includes combining the first blend and the second blend in an extruder and extruding the bio-resin from the extruder.29. The method of claim 26 , wherein the compounding includes combining the first blend and the second blend in a twin-screw extruder and extruding the bio-resin from the twin-screw extruder.30. The method of claim 26 , wherein the compounding includes combining the first blend and the second blend in an extruder and extruding the bio-resin from the extruder claim 26 , the extruder having a length to diameter ratio from 30 to 60.31. The method of claim 26 , wherein the compounding is done at a temperature of 140° C. or higher.32. The method of claim 26 , wherein forming the first blend includes combining a filler material with the agricultural byproduct having a starch content less than 50% dry weight and the plasticizer.33. The method of claim 26 , wherein forming the first blend includes combining a ...

BLACK MATRIX, METHOD FOR MANUFACTURING THE SAME AND LIQUID PANEL HAVING THE SAME

The disclosure provides a black matrix, a method for manufacturing the same and a liquid panel having the same. The black matrix is manufactured by the following steps. A mixture of resin compositions is coated on a substrate. After being dried, the black matrix is patterned by lithography. The mixture of resin compositions includes an adhesive resin, a photoinitiator, a small molecule monomer, a solvent, a light shielding material, an azo compound and an additive. According to the disclosure, the light shielding ability density of the black matrix is improved and the optical density of the black matrix of is increased by adding the azo compound having the property of polarization. Also, the usage of light shielding material in the black matrix is decreased and resistance of the black matrix is increased. 1. A black matrix , manufactured by the steps of coating a mixture of resin compositions on a substrate , drying the mixture , and patterning by lithography , wherein the mixture of resin compositions comprises an adhesive resin , a photoinitiator , a small molecule monomer , a solvent , a light shielding material , an azo compound and an additive , and the azo compound has the property of polarization.3. The black matrix according to claim 1 , wherein the light shielding material is a black inorganic pigment or a black organic pigment claim 1 , the adhesive resin is 2-(methyl) acryloyloxyethyl phthalate claim 1 , the small molecule monomer is styrene claim 1 , acrylate or methacrylate claim 1 , the photoinitiator is ethanone or 1-[9-ethyl-6 (2-methylbenzoyl)-9H-substituent carbazol-3-yl]-1-(oxo-acetyloxime) claim 1 , and the solvent is propylene glycol monomethyl ether acetate claim 1 , cyclohexanone claim 1 , 3-methoxy butyl acetate or 2-(2-butoxyethoxy)-Ethanol acetate.4. The black matrix according to claim 3 , wherein the black inorganic pigment is carbon black claim 3 , chromium oxide claim 3 , iron oxide claim 3 , titanium oxide or graphite claim 3 , and the ...

THERMOPLASTIC ELASTOMER COMPOSITION AND MOLDED PRODUCT OBTAINED THEREFROM

This invention relates to a thermoplastic elastomer composition having a type A hardness (i.e., the momentary value) of 55 or less in accordance with JIS K6253, which comprises 35 to 65 parts by weight of an olefin-based thermoplastic elastomer (A) having a type A hardness (i.e., the momentary value) of 75 or less in accordance with JIS K6253 and 65 to 35 parts by weight of a styrene-based thermoplastic elastomer (B) having a type A hardness (i.e., the momentary value) of 60 or less in accordance with JIS K6253 (with the total amount of components (A) and (B) being 100 parts by weight) and a molded thermoplastic elastomer product obtained via molding of such composition. 1. A thermoplastic elastomer composition having a type A hardness (i.e. , the momentary value) of 55 or less in accordance with JIS K6253 , which comprises 35 to 65 parts by weight of an olefin-based thermoplastic elastomer (A) having a type A hardness (i.e. , the momentary value) of 75 or less in accordance with JIS K6253 and 65 to 35 parts by weight of a styrene-based thermoplastic elastomer (B) having a type A hardness (i.e. , the momentary value) of 60 or less in accordance with JIS K6253 (with the total amount of components (A) and (B) being 100 parts by weight).2. A The thermoplastic elastomer composition according to claim 1 , wherein a compression set measured at 70° C. 24 hours later is 95% or less in accordance with JIS K6262.3. The thermoplastic elastomer composition according to claim 1 , which is obtained by adding a foaming agent (C).4. A molded thermoplastic elastomer product claim 1 , which is obtained by molding the thermoplastic elastomer composition according to .5. A foam-molded thermoplastic elastomer product claim 3 , which is obtained by molding the thermoplastic elastomer composition according to .6. The thermoplastic elastomer composition according to claim 2 , which is obtained by adding a foaming agent (C).7. A molded thermoplastic elastomer product claim 2 , which is ...

THERMOPLASTIC STARCH COMPOSITION DERIVATIVES FROM AGRICULTURAL BYPRODUCTS

A thermoplastic starch composition acquired from compounding a mixture comprises starch-containing agricultural waste in 45 to 70% by weight of total composition that the agricultural waste contains starch content less than 50% in dry weight; thermoplastic synthetic polymer in 25 to 50% by weight of total composition; plasticizer in 1 to 10% by weight of total composition; and coupling agent in 1 to 5% by weight of total composition; wherein the compounding is performed at a first temperature which is higher than room temperature. 1. A method of forming a bio-resin product , the method comprising:forming a first blend by combining an agricultural byproduct having a starch content of less than 50% by dry weight and a plasticizer;forming a second blend by combining a synthetic polymer and a coupling agent;compounding the first blend and the second blend, the compounding including combining the first blend and second blend in an extruder and coextruding the combined first blend and second blend to form a bio-resin; andforming a product from the bio-resin.2. A method , comprising: forming a bio-resin , said forming comprising:forming a first blend by combining an agricultural byproduct having a starch content of less than 50% by dry weight and a plasticizer;forming a second blend by combining a synthetic polymer and a coupling agent; andcompounding the first blend and the second blend to form a bio-resin.3. The method of claim 2 , wherein the compounding includes combining and coextruding the first blend and second blend.4. The method of claim 2 , wherein the compounding includes combining the first blend and the second blend in an extruder and extruding the bio-resin from the extruder.5. The method of claim 2 , wherein the compounding includes combining the first blend and the second blend in a twin-screw extruder and extruding the bio-resin from the twin-screw extruder.6. The method of claim 2 , wherein the compounding includes combining the first blend and the second ...

Resorbable biomimetic prosthetic ligament

An artificial ligament prosthesis which is notable in that it comprises a layer totally or partly consisting of PCL fibres. The ligament prosthesis is a biodegradable and “biointegrable” artificial ligament which makes it possible to take away all the apprehensions and uncertainties due to non-degradable synthetic supports. It is a prosthetic structure inspired by and similar to the native tissue, which is biodegradable while being sterilisable. It can optionally be seeded in order to facilitate the formation of functional tissues with controlled cell and tissue activity, having the required mechanical properties. The prosthesis maybe slowly resorbable in order to be gradually replaced with a functional tissue identical to that of the native ligament.

EXPANDABLE POLYMERIC COMPOSITION WITH IMPROVED FLEXIBILITY AND RELATIVE PREPARATION PROCESS

The present invention relates to a polymeric composition which comprises: a) vinyl aromatic polymers and/or copolymers in an amount ranging from 50% to 99% by weight, calculated with respect to the overall composition, b) a polyolefin or a relative copolymer with an ester in an amount ranging from 1% to 50% by weight, calculated with respect to the overall composition, c) olefinic elastomer grafted with a.-vinyl aromatic polymer in an amount ranging from 0.01% to 40% by weight, calculated with respect to the sum of (a)+(b), d) an expanding agent in an amount ranging from 1% to 10% by weight, calculated with respect to the sum of (a)+(b)+(c). 1. A polymeric composition which comprises:a) vinyl aromatic polymers and/or copolymers in an amount ranging from 50% to 99% by weight, calculated with respect to the overall composition,b) a polyolefin or a relative copolymer with an ester in an amount ranging from 1% to 50% by weight, calculated with respect to the overall composition,c) an olefinic elastomer grafted with a vinyl aromatic polymer in an amount ranging from 0.01% to 40% by weight, calculated with respect to the sum of (a)+(b),d) an expanding agent in an amount ranging from 1% to 10% by weight, calculated with respect to the sum of (a)+(b)+(c).2. The polymeric composition according to claim 1 , wherein the molar ratio between the vinyl aromatic polymer and the olefinic elastomer in the grafted olefinic elastomer is higher than 0.8.3. The polymeric composition according to claim 2 , wherein the molar ratio between the vinyl aromatic polymer and the olefinic elastomer in the grafted olefinic elastomer ranges from 1 to 2.4. The polymeric composition according to claim 1 , wherein components (a) and (b) are dispersed with an average diameter ranging from 10 to 2000 nm.5. The polymeric composition according to claim 1 , wherein the polyolefin is present in an amount ranging from 1% to 50% % by weight.6. The polymeric composition according to claim 1 , wherein the ...

EXPANDABLE THERMOPLASTIC RESIN PARTICLES, THERMOPLASTIC PRE-EXPANDED PARTICLES, AND THERMOPLASTIC EXPANSION-MOLDED ARTICLE

An expandable thermoplastic resin particle including a polymer obtained by a process including polymerizing monomers including 60 to 80 parts by weight of α-methylstyrene and 40 to 20 parts by weight of acrylonitrile. A content of residual monomeric components in the expandable thermoplastic resin particle is not more than 0.5% by weight. When an expanded mold article is produced from the expandable thermoplastic resin particle at an expansion ratio of 10 times, foam cells in a cross section of the expanded mold article have an average chord length of from 20 μm to 60 μm. 1. An expandable thermoplastic resin particle , comprising:a polymer obtained by a process comprising polymerizing monomers comprising 60 to 80 parts by weight of α-methyl styrene and 40 to 20 parts by weight of acrylonitrile,wherein a content of residual monomeric components in the expandable thermoplastic resin particle is not more than 0.5% by weight, andwhen an expanded mold article is produced from the expandable thermoplastic resin particle at an expansion ratio of 10 times, foam cells in a cross section of the expanded mold article have an average chord length of from 20 μm to 60 μm.2. The expandable thermoplastic resin particle according to claim 1 , wherein the expandable thermoplastic resin particle is expandable at an expansion ratio of 2 to 15 times.3. (canceled)4. The expandable thermoplastic resin particle according to claim 1 , wherein claim 1 , when an expanded mold article is produced from the expandable thermoplastic resin particle and the expanded mold article is treated at 90° C. for 24 hours claim 1 , a percentage of dimensional change of an expanded mold article caused by the treating is less than 0.15%.5. The expandable thermoplastic resin particle according to claim 1 , wherein the expandable thermoplastic resin particle has a surface layer comprising a plasticizer and a pigment.6. A thermoplastic pre-expanded particle claim 1 , produced by expanding the expandable ...

Oxygen Scavenging Composition for Plastic Material

The invention relates to the use of an additive as oxygen scavenger in a plastic material, wherein (a) the plastic material is a polyester, a polyolefin, a polyolefin copolymer or a polystyrene, and the additive (b) is a light stabilizer and optionally a transition metal compound.

GOLF BALL

An object of the present invention is to provide a golf ball exhibiting good shot feeling and excellent resilience. The present invention provides a golf ball comprising a spherical core and one or more cover layers disposed outside the spherical core, wherein at least one layer of the cover layers contains: (A) a base resin containing (a-1) an ionomer resin and having a material hardness of 59 or more in Shore D hardness; and (B) a polyrotaxane having a cyclodextrin with at least a part of hydroxyl groups of the cyclodextrin being modified with a caprolactone chain having a carboxyl group at a terminal of the caprolactone chain, a linear molecule piercing through a cyclic structure of the cyclodextrin, and blocking groups located at both terminals of the linear molecule to prevent disassociation of the cyclodextrin. 1. A golf ball comprising a spherical core and one or more cover layers disposed outside the spherical core , wherein at least one layer of the cover layers contains:(A) a base resin containing (a-1) an ionomer resin and having a material hardness of 59 or more in Shore D hardness; and(B) a polyrotaxane having a cyclodextrin with at least a part of hydroxyl groups of the cyclodextrin being modified with a caprolactone chain having a carboxyl group at a terminal of the caprolactone chain, a linear molecule piercing through a cyclic structure of the cyclodextrin, and blocking groups located at both terminals of the linear molecule to prevent disassociation of the cyclodextrin.2. The golf ball according to claim 1 , wherein (A) the base resin further contains (a-2) a non-ionomer resin.3. The golf ball according to claim 1 , wherein (B) the polyrotaxane has polyethylene glycol as the linear molecule and an adamantyl group as the blocking group.4. The golf ball according to claim 1 , wherein the cover layer containing (A) the base resin and (B) the polyrotaxane contains (B) the polyrotaxane in an amount of from 0.1 part by mass to 20 parts by mass with ...

USE OF HYBRID COPOLYMERS AS PROTECTIVE COLLOIDS FOR POLYMERS

Water-redispersible polymer powders having a high proportion of base polymer are prepared by spray drying a base polymer dispersion, employing as a spraying aid, a hybrid copolymer prepared by polymerizing an ethylenically unsaturated monomer in the presence of a water soluble polymer. 112-. (canceled)14. The process for preparing a water-redispersible polymer powder of claim 13 , wherein the ethylenically unsaturated compounds used to form the base polymer particles of A) include one or more water-insoluble ethylenically unsaturated monomers whose homopolymers have a solubility in water of <10 g/l under standard conditions according to DIN50014.15. The process for preparing a water-redispersible polymer powder of claim 13 , wherein the ethylenically unsaturated compounds used to form the base polymer particles of A) include one or more ethylenically unsaturated cationic monomers.16. The process for preparing a water-redispersible polymer powder of claim 13 , wherein the ethylenically unsaturated silanes a)ii) include one or more ethylenically unsaturated silicon compounds of the formula{'br': None, 'sup': 3', '2', '4, 'sub': 0-2', '1-3, 'R—SiR(OR)\u2003\u2003(2)'}where{'sup': '2', 'sub': 1', '3', '1', '3, 'Ris a C- to C-alkyl radical, C- to C-alkoxy radical or halogen,'}{'sup': 3', '3', '5, 'sub': 2', '2', '0-1', '2', '2', '2', '1-3, 'Ris CH═CR—(CH)or CH═CRCO(CH),'}{'sup': 4', '4, 'Ris an unbranched or branched, optionally substituted alkyl radical having 1 to 12 carbon atoms or an acyl radical having 2 to 12 carbon atoms, where Ris optionally interrupted by an ether group, and'}{'sup': '5', 'sub': '3', 'Ris H or CH.'}17. The process for preparing a water-redispersible polymer powder of claim 13 , wherein one or more water-soluble polymers b) are selected from the group consisting of polysaccharides in water-soluble form claim 13 , proteins claim 13 , lignosulfonates claim 13 , formaldehydesulfonates and polymers comprising units of vinyl alcohol claim 13 , ...

Improved Expandable Vinyl Aromatic Polymers

The present invention is related to expandable vinyl aromatic polymers comprising comminuted coke, said comminuted coke having an average stack height (Lc) of carbon crystallites at least 4 nm, a volume median particle diameter (D50) comprised between 1 and less than 5 μm and being characterized by a span (D90−D10)/D50 below 2.5 Molded parts produced from the expandable vinyl aromatic polymers prove low thermal conductivities for a low foam density.

MAGENTA INK FOR INKJET

The invention provides a magenta ink for inkjet which yields distinct images having high gloss and no density irregularities or voids upon inkjet printing onto low-absorption substrates, exhibits excellent discharge stability after long standby periods, and can provide excellent drying properties even during high-speed printing; and also provides an ink set that can suppress mixed color bleeding and achieve superior color reproducibility.

INK COMPOSITION , WRITING TOOL AND METHOD FOR PRODUCING INK COMPOSITION

The ink composition contains titanium oxide particles having an average particle size of 0.1 μm or more and 0.4 μm or less, hollow resin particles having an average particle size of 1.0 μm or more and 2.0 μm or less, a polysaccharide and water, wherein the titanium oxide particles and the hollow resin particles are negatively charged. 1. An ink composition comprising:titanium oxide particles having an average particle size of 0.1 μm or more and 0.4 μm or less;hollow resin particles having an average particle size of 1.0 μm or more and 2.0 μm or less;a polysaccharide; andwater; whereinthe titanium oxide particles and the hollow resin particles are negatively charged.2. The ink composition according to claim 1 , wherein the hollow resin particles are devoid of a colouring material adsorbed thereto.3. The ink composition according to claim 1 , wherein the hollow resin particles contain styrene-acrylic copolymer particles.4. The ink composition according to claim 1 , wherein the titanium oxide particles have an oil absorption of 29 g/100 g or more and 35 g/100 g or less.5. The ink composition according to claim 1 , comprising:5.0 wt % or more and 40.0 wt % or less of the titanium oxide particles; and5.0 wt % or more and 20.0 wt % or less of the hollow resin particles.6. The ink composition according to claim 1 , further comprising a surfactant.7. The ink composition according to claim 6 , wherein the surfactant contains a silicone active agent.8. The ink composition according to claim 1 , further comprising a film-forming resin.9. The ink composition according to claim 8 , wherein the film-forming resin contains at least one of an acrylic resin or a polyester resin.10. The ink composition according to claim 9 , wherein the polyester resin is a saturated polyester resin.11. The ink composition according to claim 1 , further comprising a colouring material.12. A writing tool comprising:a writing section; and{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'an ink storage ...

WOOD ADHESIVE

A wood adhesive is provided. The wood adhesive includes a first agent and a second agent. The first agent includes a sodium carboxymethyl cellulose and a styrene-butadiene rubber polymer. The sodium carboxymethyl cellulose has a molecular weight between 15,000 and 500,000 and a degree of substitution of from 0.4 to 2.00 of the sodium salt. The second agent includes a polymeric quaternary amine. 1. A method for forming a wood adhesive , comprising:providing a first agent, comprising:preparing a water solution of sodium carboxymethyl cellulose comprising a sodium carboxymethyl cellulose having a molecular weight between 15,000 and 500,000 and a degree of substitution of from 0.4 and 2.00 of the sodium salt; andadding a styrene-butadiene rubber polymer in the water solution of sodium carboxymethyl cellulose; andadding NaOH in the water solution of sodium carboxymethyl cellulose mixed with the styrene-butadiene rubber polymer;providing a second agent, comprising a polymeric quaternary amine; andmixing the first agent and the second agent;wherein a ratio of the weight of the styrene-butadiene rubber polymer to the sum of weights of the sodium carboxymethyl cellulose and the polymeric quaternary amine is in the range from 0.05:1 to 1:0.1.2. The method according to claim 1 , wherein a weight ratio of the first agent to the second agent is in the range from 0.25:1 to 1:0.05.3. The method according to claim 1 , wherein a weight ratio of the first agent to the second agent is in the range from 0.7:1 to 1:0.2.4. The method according to claim 1 , wherein a weight ratio of the sodium carboxymethyl cellulose to the polymeric quaternary amine is in the range from 0.05:1 to 1:0.05.5. The method according to claim 1 , wherein the second agent further comprises water claim 1 , and the polymeric quaternary amine exists in aqueous phase.6. The method according to claim 1 , wherein the polymeric quaternary amine is formed by the reaction of polyamidoamine with epichlorohydrin.7. The ...

Paraffin deposition inhibitor coatings

A containment for crude oil that inhibits paraffin deposition thereon is described. One to twenty coatings of a composition including a polyacrylate are applied to a crude oil contact surface of a crude oil containment; the polyacrylate includes at least about 50 mole % acrylic acid residues or the conjugate base thereof. The coating compositions are suitably delivered from a water dispersion, solution, or emulsion and dried before applying a subsequent coating. Each of the one to twenty coatings are formed from the same or from different polyacrylate coating compositions. The coated containment surfaces inhibit deposition of at least 10 wt % and as much as 90 wt % of paraffin solids from a crude oil compared to the same crude oil contact in the absence of the one to twenty coatings. The coatings inhibit paraffin deposition at temperatures between about 60° C. and −40° C.

THERMOPLASTIC STARCH COMPOSITION DERIVATIVES FROM AGRICULTURAL BYPRODUCTS

A thermoplastic starch composition acquired from compounding a mixture comprises starch-containing agricultural waste in 45 to 70% by weight of total composition that the agricultural waste contains starch content less than 50% in dry weight; thermoplastic synthetic polymer in 25 to 50% by weight of total composition; plasticizer in 1 to 10% by weight of total composition; and coupling agent in 1 to 5% by weight of total composition; wherein the compounding is performed at a first temperature which is higher than room temperature. 1. A method of forming a bio-resin product , the method comprising:forming a first blend by combining an agricultural byproduct having a starch content of less than 50% by dry weight and a plasticizer;forming a second blend by combining a synthetic polymer and a coupling agent;compounding the first blend and the second blend, the compounding including combining the first blend and second blend in an extruder and coextruding the combined first blend and second blend to form a bio-resin; andforming a product from the bio-resin.2. A method , comprising: forming a bio-resin , said forming comprising:forming a first blend by combining an agricultural byproduct having a starch content of less than 50% by dry weight and a plasticizer;forming a second blend by combining a synthetic polymer and a coupling agent; andcompounding the first blend and the second blend to form a bio-resin.3. The method of claim 2 , wherein the compounding includes combining and coextruding the first blend and second blend.4. The method of claim 2 , wherein the compounding includes combining the first blend and the second blend in an extruder and extruding the bio-resin from the extruder.5. The method of claim 2 , wherein the compounding includes combining the first blend and the second blend in a twin-screw extruder and extruding the bio-resin from the twin-screw extruder.6. The method of claim 2 , wherein the compounding includes combining the first blend and the second ...

Molded body and production method thereof

Disclosed is a molded body and a method for producing the same. The molded body includes: a continuous phase containing first and second polyolefin resins; and a dispersed phase containing a polyamide resin and a modified elastomer and composed of a melt-kneaded product of the polyamide resin and the modified elastomer, the modified elastomer has a reactive group that reacts with the polyamide resin, the elastomer is an olefin-based thermoplastic elastomer having, as a skeleton, a copolymer of ethylene or propylene and an α-olefin having 3-8 carbon atoms or a styrene-based thermoplastic elastomer having a styrene skeleton, when a total of the continuous and dispersed phases is taken as 100% by mass, the dispersed phase is 70% by mass or less, and when a total of the first and second polyolefin resins is taken as 100% by mass, the second polyolefin resin is 80% by mass or less.

NEGATIVE PHOTOSENSITIVE COMPOSITION, ARTICLE CURED THEREFROM, AND METHOD FOR CURING SAID COMPOSITION

Provided are: a negative photosensitive composition which exhibits excellent sensitivity at the time of being cured and yields a cured article having excellent heat resistance; a cured article thereof; and a method of curing the same. The negative photosensitive composition contains: a sulfonic acid derivative compound (A) represented by Formula (I) below where Xrepresents a linear or branched alkyl group having 1 to 14 carbon atoms or the like; Rrepresents an aliphatic hydrocarbon group having 1 to 18 carbon atoms or the like; and the aliphatic hydrocarbon group having 1 to 18 carbon atoms or the like has no substituent or is optionally substituted with a halogen atom or a group selected from a halogenated alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 18 carbon atoms and an alkylthio group having 1 to 18 carbon atoms; a crosslinkable functional group-containing polymer compound (B); and a crosslinking agent (C): 19-. (canceled)11. The negative photosensitive composition according to claim 10 , wherein Xis an alkyl group having 3 to 8 carbon atoms.12. The negative photosensitive composition according to claim 10 , wherein Xis an alkyl group having 4 carbon atoms.13. The negative photosensitive composition according to claim 10 , wherein Ris a perfluoroalkyl group having 1 to 8 carbon atoms.14. The negative photosensitive composition according to claim 10 , wherein the crosslinkable functional group-containing polymer compound (B) is a polyhydroxystyrene resin claim 10 , an epoxy resin claim 10 , an epoxy acrylate resin or epoxy methacrylate resin having at least one substituent selected from a hydroxy group and a carboxyl group claim 10 , or a novolac resin having a hydroxy group claim 10 , an epoxy group or a carboxyl group.16. The negative photosensitive composition according to claim 10 , wherein the crosslinkable functional group-containing polymer compound (B) is an epoxy acrylate resin or epoxy methacrylate resin having a structure in ...

Magnetic particles for diagnostics

The organic polymer particles comprise a carboxyl group and 2,3-dihydroxypropyl group, and the magnetic particles for diagnostics comprise fine magnetic material particles and a polymer part containing a hydrophilic polymer part and a crosslinked polymer part, a dry coating film obtained from a water dispersion thereof having a contact angle with water of 5° to 60°. The process for producing the carboxyl group-containing particles comprises a step of producing an ester bond by reacting a hydroxyl group in organic polymer particles having the hydroxyl group with a carboxylic anhydride. The organic polymer particles comprise a hydroxyl group originating from a 2,3-dihydroxypropyl group and a polyoxyethylene group.

Organic polymer particles and process for producing the same, magnetic particles for diagnostics, carboxyl group-containing particles and process for producing the same, and probe-bound particles and process for producing the same

The organic polymer particles comprise a carboxyl group and 2,3-dihydroxypropyl group, and the magnetic particles for diagnostics comprise fine magnetic material particles and a polymer part containing a hydrophilic polymer part and a crosslinked polymer part, a dry coating film obtained from a water dispersion thereof having a contact angle with water of 5° to 60°. The process for producing the carboxyl group-containing particles comprises a step of producing an ester bond by reacting a hydroxyl group in organic polymer particles having the hydroxyl group with a carboxylic anhydride. The organic polymer particles comprise a hydroxyl group originating from a 2,3-dihydroxypropyl group and a polyoxyethylene group.

Organic polymer particles and process for producing the same, magnetic particles for diagnostics, carboxyl group-containing particles and process for producing the same, and probe-bound particles and process for producing the same

The organic polymer particles comprise a carboxyl group and 2,3-dihydroxypropyl group, and the magnetic particles for diagnostics comprise fine magnetic material particles and a polymer part containing a hydrophilic polymer part and a crosslinked polymer part, a dry coating film obtained from a water dispersion thereof having a contact angle with water of 5° to 60°. The process for producing the carboxyl group-containing particles comprises a step of producing an ester bond by reacting a hydroxyl group in organic polymer particles having the hydroxyl group with a carboxylic anhydride. The organic polymer particles comprise a hydroxyl group originating from a 2,3-dihydroxypropyl group and a polyoxyethylene group.

Organic polymer particles and process for producing the same, magnetic particles for diagnostics, carboxyl group-containing particles and process for producing the same, and probe-bound particles and process for producing the same

The organic polymer particles comprise a carboxyl group and 2,3-dihydroxypropyl group, and the magnetic particles for diagnostics comprise fine magnetic material particles and a polymer part containing a hydrophilic polymer part and a crosslinked polymer part, a dry coating film obtained from a water dispersion thereof having a contact angle with water of 5° to 60°. The process for producing the carboxyl group-containing particles comprises a step of producing an ester bond by reacting a hydroxyl group in organic polymer particles having the hydroxyl group with a carboxylic anhydride. The organic polymer particles comprise a hydroxyl group originating from a 2,3-dihydroxypropyl group and a polyoxyethylene group.

Micronized asphalt modifiers, methods of modifying asphalt, asphalt compositions and methods of making

An asphalt additive comprising a primary rheology modifying component and a secondary rheology modifying component, and asphalt compositions and products having such additive incorporated therein. The primary rheology modifying component is generally a polymer, and the secondary rheology modifying component may comprise a petroleum micro-wax.

Blends of polypropylene with hydrogenated hydrocarbon resins

Blends of polypropylene with hydrogenated polymers and copolymers of styrene. The useful polymers have a precisely defined molecular weight distribution and must be hydrogenated to the point where at least 50 percent of the aromatic unsaturation is reduced. The blends are useful in preparation of heat sealable films and capacitor dielectrics.

Unoriented film based on soft polypropylene

Unoriented film comprising at least one layer of a polymer composition comprising a styrenic based elastomer and a propylene copolymer.

Flameproof expandable styrene polymers, and method for the production thereof

Disclosed are expandable styrene polymers (EPS) containing, in relation to the styrene polymer, a) 0.05 to 5 percent by weight of an organic bromine compound containing a minimum of 50 percent by weight of bromine as a flameproofing agent, b) 0.05 to 2 percent by weight of a flameproofing synergist, c) 1 to 5 percent by weight of a metallic salt as an acid collector. Also disclosed is a method for producing said expandable styrene polymers.

丙烯类树脂组合物、丙烯类树脂组合物的制造方法、丙烯类聚合物组合物、由该丙烯类树脂组合物形成的成型体和电线

本发明的丙烯类树脂组合物的特征在于，含有：(A)用差示扫描量热计观测到的熔点为100℃以上的丙烯类聚合物0～80重量％；(B)特定的软质丙烯类共聚物5～85重量％；(C)选自乙烯类弹性体(C1)和苯乙烯类弹性体(C2)中的一种以上的弹性体合计0～40重量％；和(D)无机类填料15～80重量％(其中，(A)、(B)、(C)和(D)成分的合计量为100重量％)。本发明的丙烯类树脂组合物含有高比例的无机类填料，并且具有良好的柔软性，同时具有优异的断裂伸长、低温特性、耐白化性和耐损伤性、耐磨损性、应力吸收性和阻燃性。

Breathable films and method for making

The present invention relates to a cold-drawn breathable film formed from a blend of a soft polymer component and a hard polymer component. The soft polymer component (SPC) is a copolymer of a major olefinic monomer and a minor olefinic monomer. The major olefinic monomer is either ethylene or propylene and forms the majority of the SPC. Preferred films after cold-drawing exhibit a water vapor transmission rate (WVTR) of at least 100 g-mil/m 2 -day.

COMPOSITIONS OF INTERPOLYMERS OF α-OLEFIN MONOMERS WITH ONE OR MORE VINYL OR VINYLIDENE AROMATIC MONOMERS AND/OR ONE OR MORE HINDERED ALIPHATIC OR CYCLOALIPHATIC VINYL OR VINYLIDENE MONOMERS BLENDED WITH A CONDUCTIVE ADDITIVE

A blend of polymeric materials comprising (A) of from about 1 to about 99.99 weight percent based on the combined weights of Components A, B and C of at least one substantially random interpolymer; and wherein said interpolymer; (1) contains of from about 0.5 to about 65 mole percent of polymer units derived from; (a) at least one vinyl or vinylidene aromatic monomer, or (b) at least one hindered aliphatic or cycloaliphatic vinyl or vinylidene monomer, or (c) a combination of at least one vinyl or vinylidene aromatic monomer and at least one hindered aliphatic or cycloaliphatic vinyl or vinylidene monomer; (2) contains of from about 35 to about 99.5 mole percent of polymer units derived from at least one aliphatic α-olefin having from 2 to 20 carbon atoms; (3) has a molecular weight (Mn) greater than about 1,000; (4) has a melt index (I 2 ) of from about 0.01 to about 1,000; (5) has a molecular weight distribution (M w /M n ) of from about 1.5 to about 20; and (B) of from about 99 to about 0.01 weight percent based on the combined weights of Components A, B, and C of one or more conductive additives and/or one or more additives with high magnetic permeability ; and (C) of from 0 to about 98.99 weight percent based on the combined weights of Components A, B, and C of one or more polymers other than A.

Open-cell foam and method of making

Soft and flexible foams made from blends of alkenyl aromatic polymers and alpha-olefin/vinyl or vinylidene aromatic and/or sterically hindered aliphatic or cycloaliphatic vinyl or vinylidene interpolymers

A soft foam having an Asker C hardness of less than about 65, comprising; (A) from about 30 to about 70 percent by weight (based on the combined weight of Components A and B) of one or more alkenyl aromatic polymers and wherein at least one of said alkenyl aromatic polymers has a molecular weight (M w ) of from about 100,000 to about 500,000; and (B) from about 30 to about 70 percent by weight (based on the combined weight of Components A and B) of one or more substantially random interpolymers having an I 2 of about 0.1 to about 50 g/10 min, an M w /M n of about 1.5 to about 20; comprising (1) from about 8 to about 45 mol % of polymer units derived from; (a) at least one vinyl or vinylidene aromatic monomer, or (b) at least one hindered aliphatic or cycloaliphatic vinyl or vinylidene monomer, or (c) a combination of at least one aromatic vinyl or vinylidene monomer and at least one hindered aliphatic or cycloaliphatic vinyl or vinylidene monomer, and (2) from about 55 to about 92 mol % of polymer units derived from at least one of ethylene and/or a C 3-20 α-olefin; and (3) from 0 to about 20 mol % of polymer units derived from one or more of ethylenically unsaturated polymerizable monomers other than those derived from (1) and (2); and (C) optionally, one or more nucleating agents; and (D) optionally, one or more other additives; and (E) one or more blowing agents present in a total amount of from about 0.4 to about 5.0 gram-moles per kilogram (based on the combined weight of Components A and B).

Acoustical insulation foams

An acoustical insulation foam having, either with or without elastification, an Asker C hardness of less than about 65, a density of about 5 to about 150 kg/m3, a cell size of about 0.05 to about 15 mm, an open cell content of 0 to about 100 volume percent, a thickness of about 1 to about 200 mm, and a width of about 100 to about 3000 mm; comprising; (A) one or more alkenyl aromatic polymers, (B) one or more substantially random interpolymers and (C) optionally, one or more nucleating agents and (D) optionally, one or more other additives; and (E) one or more blowing agents.

Thermoplastic compositions for durable goods applications

Thermoplastic compositions have been discovered which are suitable for rotational molding. The compositions have improved processability and/or improved physical and mechanical properties. The compositions advantageously often exhibit one or more of the following: reduced low shear viscosity, reduced melt elasticity at low shear rate, reduced cycle times, improved sintering and a wide range of processing temperatures, improved low temperature and/or room temperature impact, good environmental stress crack resistance, acceptable heat distortion temperature, and acceptable flexural and secant modulus.

Thermoformable ethylene/styrene interpolymer-based polymer blend film for three-dimensional transfer finish foil

Thermoformable films that contain a blend and/or composite structure containing an ethylene/vinyl or vinylidene aromatic polymer or an alpha-olefin/vinyl or vinylidene aromatic polymer, such as an ethylene/styrene interpolymer, a vinyl or vinylidene aromatic homo- or copolymer, such as polystyrene, and, optionally, an alpha-olefin homo- or copolymer serve as effective carrier layers for heat transfer foils.

Open-cell foam and method of making

An open-cell polystyrene foam is provided which is formed from a blend of polystyrene and an ethylene-styrene interpolymer. The ethylene-styrene interpolymer functions as a cell opening agent, and is used to control the open cell content of the resulting foam, which may contain greater than 80 percent open cells. The foam is produced by an extrusion process in which carbon dioxide is used as the preferred blowing agent. The resulting foams may be formed into beads, plank, round, sheets, etc.

Acoustical insulation foams

An acoustical insulation foam having, either with or without elastification, an Asker C hardness of less than about 65, a density of about 5 to about 150 kg/m3, a cell size of about 0.05 to about 15 mm, an open cell content of 0 to about 100 volume percent, a thickness of about 1 to about 200 mm, and a width of about 100 to about 3000 mm; comprising; (A) one or more alkenyl aromatic polymers, (B) one or more substantially random interpolymers and (C) optionally, one or more nucleating agents and (D) optionally, one or more other additives; and (E) one or more blowing agents.

Thermoformable ethylene/styrene interpolymer-based polymer blend film for three-dimensional transfer finish foil

Thermoformable films that contain a blend and/or composite structure containing an ethylene/vinyl or vinylidene aromatic polymer or an alpha-olefin/vinyl or vinylidene aromatic polymer, such as an ethylene/styrene interpolymer, a vinyl or vinylidene aromatic homo- or copolymer, such as polystyrene, and, optionally, an alpha-olefin homo- or copolymer serve as effective carrier layers for heat transfer foils.

Acoustical insulation foams

An acoustical insulation foam having, either with or without elastification, an Asker C hardness of less than about 65, a density of about 5 to about 150 kg/m3, a cell size of about 0.05 to about 15 mm, an open cell content of 0 to about 100 volume percent, a thickness of about 1 to about 200 mm, and a width of about 100 to about 3000 mm; comprising; (A) one or more alkenyl aromatic polymers, (B) one or more substantially random interpolymers and (C) optionally, one or more nucleating agents and (D) optionally, one or more other additives; and (E) one or more blowing agents.

Polyolefin material with enhanced surface durability

Thermoplastic polyolefin blends with a good stiffness/impact balance, as well as enhanced surface durability, contain semi-crystalline polypropylene resin component, a propylene-based elastomer component, and an optional but preferred styrene-based elastomer component. The propylene-based elastomer (PBE) is characterized as having at least one of a) a plurality of identifying band positions at 998 cm −1 , 974 cm −1 , and 733 cm −1 , as measured by Fourier Transform Infrared Spectroscopy (FTIR); or one or more glass transition temperatures (Tg) from about −15° C. to −35° C., as measured by Differential Scanning Calorimetry. The surface of articles made from such a thermoplastic blend shows increased scratch resistance and a decrease in stress whitening.

High impact resistant, high gloss, and high environmental stress crack resistant thermoplastic manufactured articles

Thermoplastic manufactured articles are provided which exhibit an advantageous combination of high gloss and high environmental stress crack resistance, made from a polymeric composition comprising: (a) high impact polystyrene having a gloss at 60 degrees of greater than 85% and an impact resistance of greater than 0.7 ft-lb/inch; (b) high density polyethylene which has a density greater than or equal to about 0.94 g/cm3, and which has a stress exponent less than or equal to about 1.70; and (c) a compatibilizing polymer for components (a) and (b), selected from the group consisting of diblock styrene butadiene copolymers, triblock styrene butadiene copolymers, diblock styrene isoprene copolymers, triblock styrene isoprene copolymers, and mixtures thereof, wherein the gloss at 60 degrees of the composition is greater than or equal to about 85%, and the environmental stress crack resistance measured in minutes until breakage at 1000 psi is greater than about 60.

Elastomer composition which is reinforced with a functionalised polyvinylaromatic filler

The invention relates to a rubber composition that is based on at least one diene elastomer, a polymer filler by way of a reinforcing filler and a coupling agent which binds the polymer filler and the elastomer. The invention is characterised in that the polymer filler comprises nanoparticles of polyvinylaromatic (PVAr) bearing a function F having formula = Si _ X, wherein X represents a hydroxyl or hydrolysable group. The PVAr comprises, for example, a copolymer of styrene, ethylvinylbenzene, divinylbenzene and (meth)acrylate of trimethoxysilylpropyl, in the form of nanoshells with a diameter of between 10 and 100 nm. The polymer filler has a very low density and, as such, can be used to reduce the weight of the inventive compositions without degradation of the reinforcement and with a notable reduction in hysteresis. The invention also relates to a method of obtaining one such composition and to a masterbatch containing at least one diene elastomer and one such polymer filler and to the method of obtaining one such masterbatch. The invention further relates to the use of one such rubber composition for the production of rubber articles, particularly tyres or semi-finished products made from rubber that are intended for said tyres.

Compositions of interpolymers of alpha-olefin monomers with one or more vinyl or vinylidene aromatic monomers and/or one or more hindered aliphatic or cycloaliphatic vinyl or vinylidene monomers blended with a conductive additive

A blend of polymeric materials comprising (A) of from about 1 to about 99.99 weight percent based on the combined weights of Components A, B and C of at least one substantially random interpolymer; and wherein said interpolymer; (1) contains of from about 0.5 to about 65 mole percent of polymer units derived from; (a) at least one vinyl or vinylidene aromatic monomer, or (b) at least one hindered aliphatic or cycloaliphatic vinyl or vinylidene monomer, or (c) a combination of at least one vinyl or vinylidene aromatic monomer and at least one hindered aliphatic or cycloaliphatic vinyl or vinylidene monomer; (2) contains of from about 35 to about 99.5 mole percent of polymer units derived from at least one aliphatic α-olefin having from 2 to 20 carbon atoms; (3) has a molecular weight (Mn) greater than about 1,000; (4) has a melt index (I 2 ) of from about 0.01 to about 1,000; (5) has a molecular weight distribution (M w /M n ) of from about 1.5 to about 20; and (B) of from about 99 to about 0.01 weight percent based on the combined weights of Components A, B, and C of one or more conductive additives and/or one or more additives with high magnetic permeability; and (C) of from 0 to about 98.99 weight percent based on the combined weights of Components A, B, and C of one or more polymers other than A.

Modified polyethylene film compositions

The present invention relates to polyethylene compositions comprising one or more ethylene polymers and one or more dendritic hydrocarbon polymer modifiers, in particular, this invention further relates to polyethylene blends comprising one or more ethylene polymers and one or more dendritic hydrocarbon polymer modifiers, wherein the modifier has: 1) a g′ value less than 0.75; 2) a Cayley tree topology with a layer number of 2 or more more; and 3) a average Mw between the branch points of 1,500 g/mol or more.

Magnetic particles for diagnostics

Magnetic particles for diagnostics

Organic polymer particles and process for producing the same, magnetic particles for diagnostics, carboxyl group-containing particles and process for producing the same, and probe-bound particles and process for producing the same

Organic polymer particles and process for producing the same, magnetic particles for diagnostics, carboxyl group-containing particles and process for producing the same, and probe-bound particles and process for producing the same

Organic polymer particles and methods of preparation therefor, magnetic particles for diagnosis, particles having a carboxyl group and methods of preparation therefor, and probe-bound particles and methods of preparation thereof

Organic polymer particles and methods of preparation therefor, magnetic particles for diagnosis, particles having a carboxyl group and methods of preparation therefor, and probe-bound particles and methods of preparation thereof

Organic polymer particles and process for producing the same, magnetic particles for diagnostics, carboxyl group-containing particles and process for producing the same, and probe-bound particles and process for producing the same

The organic polymer particles comprise a carboxyl group and 2,3-dihydroxypropyl group, and the magnetic particles for diagnostics comprise fine magnetic material particles and a polymer part containing a hydrophilic polymer part and a crosslinked polymer part, a dry coating film obtained from a water dispersion thereof having a contact angle with water of 5° to 60°. The process for producing the carboxyl group-containing particles comprises a step of producing an ester bond by reacting a hydroxyl group in organic polymer particles having the hydroxyl group with a carboxylic anhydride. The organic polymer particles comprise a hydroxyl group originating from a 2,3-dihydroxypropyl group and a polyoxyethylene group.

Light lignocellulosic materials having good mechanical properties

The invention relates to a method for producing a light lignocellulosic material having an average density in the range of 200 to 600 kg/m 3 , where: A) 30 to 95% by weight of lignocellulose particles; B) 1 to 25% by weight of expanded plastic particles having a bulk density in the range of 10 to 100 kg/m 3 ; C) 3 to 50% by weight of a binding agent, selected from the group of aminoplast resin, phenol formaldehyde resin, and organic isocyanate having at least two isocyanate groups and optionally D) additives are mixed and pressed under increased temperature and increased pressure, characterized in that the expanded plastic particles are obtained from expandable plastic particles by expanding, and the expanded plastic particles thus obtained are further used for producing the light lignocellulosic material without further intermediate steps.

Lignocellulose materials having good mechanical properties

A process for producing a lignocellulose-containing substance with a mean density in the range from more than 600 to 900 kg/m3, in which, based in each case on the lignocellulose-containing substance: A) 30 to 95% by weight of lignocellulose paricles; B) 1 to 25% by weight of expanded polymer particles with a bulk density in the range from 10 to 100 kg/m3; C) 3 to 50% by weight of a binder selected from the group consisting of amino resin, phenol-formaldehyde resin and organic isocyanate having at least two isocyanate groups, and optionally D) additives are mixed, and then pressed at elevated temperature and under elevated pressure.

Detergent resin composition

A detergent resin composition is provided which is, in a small quantity, capable of very effectively deterging the inside of molding machines in a short period of time at the time of change-over of chlorine-containing resins inside the machines, which composition is obtained by blending 50 to 95% by weight of a polystyrene resin, 0.1 to 15% by weight of a polymethyl methacrylate, 2 to 30% by weight of a neutral salt of a sulfonic acid and 0.1 to 10% by weight of basic magnesium carbonate, magnesium hydroxide, aluminum hydroxide, zinc carbonate or a mixture thereof, the respective proportions being based upon the weight of the composition.

Resin composite material

Styrene polymer, styrene copolymer, rubber composition, and pneumatic tire

This invention relates to a styrene-based (co)polymer capable of improving tan δ of a rubber composition while ensuring a fracture resistance of the rubber composition by adding to the rubber composition, and more particularly to a styrene-based polymer obtained by homopolymerizing a styrene derivative and having a weight average molecular weight as converted to polystyrene of 2×10 3 to 50×10 3 , and a styrene-based copolymer obtained by copolymerizing styrene and at least one of styrene derivatives and having a weight average molecular weight as converted to polystyrene of 2×10 3 to 50×10 3 .

Adhesive layer for transparent conductive film, transparent conductive film with adhesive layer, transparent conductive laminate, and touch panel