Kraton Polymers LLC

Kraton Corporation

Kraton Polymers U.S. LLC

Milliken + Co

Kraton Polymers Research B.v.

Kraton Polymers Nederland B.v.

Ruidong Ding

Jason Tian

Chad Reiter

Xavier Muyldermans

Huixian Yang

Frank Wijnand De Wit

Hannes Hendrik Peter Van Erp

Robert Charles Bening

Nathan A Mehl

David Romme Hansen

Daniel M Connor

Frank De Wit

Yaming Niu

Bing Yang

Vijay Mhetar

Koen Van Duin

Roger Tocchetto

Yonghua Zhou

Catherine Maris

Liqiang Ma

Donna Rucker

Jiaqi Yan

Sanesh Deshmukh

Richard Ma

Polymers are obtained by polymerizing in the presence of a Bronsted acid or a Lewis acid catalyst, a monomer comprising a 1,3-diisoalkenylarene, a 1,4-diisoalkenylarene, or mixtures thereof. The polymer comprises at least one of repeat units (A), (B), (C), and (D); wherein Ris H or a C1-C8 alkyl group. The polymers have high Tand exhibit good solubility in non-polar solvents, forming substantially gel-free solutions. The polymers are useful for producing crosslinked materials having good physical properties. The crosslinked materials are valuable for further downstream uses, such as copper clad laminates.

Polymers based on diisoalkenylarenes and uses thereof

The disclosure relates to methods for producing poly(cyclohexadiene) homopolymers (PCHD). The PCHD is formed by polymerizing a 1,3-cyclohexadiene monomer in the presence of a catalyst, in a hydrocarbon solvent, and at a temperature of −100° C. to 120° C. The catalyst is selected from the group consisting of a Bronsted acid, a Lewis acid, and combinations thereof. PCHD produced under these conditions has good solubility in non-polar solvents, and a number average molecular weight of 300 to 5,000 Dalton; a weight average molecular weight of 5,000 to 15,000 Delton; and a polydispersity index of 3.0 to 8.0. The PCHD is useful for producing crosslinked materials having good physical properties. The crosslinked materials can be combined with a rubbery polymer to produce compositions valuable for further downstream uses.

Poly(cyclohexadiene) homopolymer based compositions and uses thereof

Disclosed herein are copolymers formed by cationic polymerization of one or more cyclic dienes and a comonomer selected from the group consisting of a monoterpene, a branched styrene, and combinations thereof, in the presence of a catalyst. Random copolymers having repeat units derived from a cyclic conjugated diene, such as 1,3-cyclohexadiene, and a comonomer such as a monoterpene, can be prepared as soluble products in hydrocarbon solvents. The copolymers can be crosslinked with various crosslinking agents to form materials having good oxidative stability and fire retardancy. The uncrosslinked and crosslinked copolymers have useful properties such as a low dissipation factor, low dielectric constants, and a good balance of thermomechanical and electrical properties that make them valuable in electronic applications.

Cyclic diene-based copolymers

A polymer composition comprising a star-branched copolymer having a plurality of arms is disclosed. Each polymer arm has a molecular weight Mp of from 1 kg/mol to 50 kg/mol and comprises polymerized units (i) derived from a first vinyl aromatic monomer comprising a radical-reactive group, wherein from greater than 10 mol % to 100 mol % of the units (i) are unhydrogenated; and optionally, polymerized units (ii) comprising hydrogenated and unhydrogenated forms of polymerized units derived from a high Tg monomer, and hydrogenated form of polymerized units (i) or hydrogenated form of polymerized styrene units; and optionally, polymerized units (iii) comprising (a) hydrogenated form of polymerized units derived from one or more acyclic conjugated dienes, and (b) polymerized units derived from one or more of a second vinyl aromatic monomer; wherein less than 10 wt. % of units (a) are unhydrogenated.

Block copolymers and uses thereof

A resin composition that allows production of laminated sheets excellent in heat resistance and processability is disclosed. The resin composition comprises: a) a block copolymer, where the block copolymer comprises at least one polymer block comprising polymerized acyclic conjugated diene units, such as butadiene units, and at least one polymer block containing units like a conjugated cyclic diene such as 1,3-cyclohexadiene or monomer units characterized by unit Tg above 100&#xb0; C., b) a curing initiator, and c) optionally diene-based polymer selected from a polybutadiene polymer and the copolymer of butadiene with styrene or other styrenic monomers, c) optional additives comprising but not limited to a multi-functional co-curable additive, a diene based rubber, a halogenated or non halogenated flame retardant, an inorganic or organic filler or fiber, an antioxidant, a adhesion promotor, a film forming.

Block copolymer compositions, prepregs, and laminates made therefrom

A process for deodorizing a rosin ester composition is disclosed. The process employs an adsorptive bed containing an adsorbent material. The adsorbent material comprises silica adsorbent having an average pore size between 50-200 &#x212b;, BET surface area of at least 300 m/g, pore volume of 1.20 to 3.00 cc/g, and a silanol [Si&#x2014;OH] level of 0.5 to 5 unit/nm. The deodorized rosin ester composition has an odor intensity reduction of at least 1 unit on odor intensity scale of Offensive Odor Control Act as compared to the rosin ester feedstock. In embodiment, the deodorizing treatment comprises using multi-staged adsorbent system with an adsorbent column having multiple layers of different adsorbent materials.

Deodorized rosin ester and methods for making

A process for reducing or removing at least 90% of sulfur in a tall oil composition, e.g., to a level of 15 ppm or less is disclosed. The process employs at least a first desulfurization and a second desulfurization treatment in parallel or in series. The first treatment comprises adsorptive desulfurization, wherein the adsorbent material comprises silica adsorbent having an average pore size between 50-200 &#x212b;, BET surface area of at least 300 m/g, pore volume of 1.20 to 3.00 cc/g, and a silanol [Si&#x2014;OH] level of 0.5 to 5 unit/nm. The second desulfurization treatment is selected from adsorptive treatment, heat treatment, distillation, extraction, oxidation, reduction, hydrogenation, and sulfur scavenging for a reduced sulfur content.

Desulfurized tall oil and derivatives thereof

Provided herein are improved performance high vinyl block copolymer compositions. The compositions may include a block copolymer and a polyolefin. The block copolymer may have a microstructure characterized by a vinyl content of equal to or greater than about 60%. The block copolymer may be a styrenic block copolymer. The polyolefin may include a polypropylene. Additional additives may be optionally added to the composition depending on the end-use application. The compositions may find utility in the preparation of various articles such as medical products including sterilized tubing, bags, and the like, films and injection molded articles.

Performance high vinyl block copolymer compositions and uses thereof

Compositions comprising (i) a hydrogenated styrenic block copolymer, (ii) an oil, and (iii) optional additives are described herein. Compositions include but are not limited to cable fillings. The styrenic block copolymer having peak molecular weight of from about 125 to about 300 kg/mol, an oil and optional additives are described herein. The block copolymer includes a B block having vinyl content of from about 35% to about 49% and an S block having a polystyrene content of from about 28% to about 40%. The compositions may form a gel having a thixotropic ratio at 25&#xb0; C. of from about 5 to about 10 and further characterized by specific low, middle and high shear rate viscosities at 25&#xb0; C. and shear rates of 6 s, 50 sand 200 sof from 10,000 cps to 750,000 cps, 1,000 cps to 100,000 cps and 1,000 cps to 6,000 cps, respectively; a drop point from 100&#xb0; C. to 250&#xb0; C.; and a cone penetration at 25&#xb0; C. of from 300 dmm to 685 dmm.

Block copolymers for gel compositions

A novel block copolymer composition including a hydrogenated block copolymer that has at least one block A and at least one block B, and wherein (a) prior to hydrogenation each A block is a mono alkenyl arene homopolymer block and each B block is a controlled distribution copolymer block of at least one conjugated diene and at least one mono alkenyl arene, (b) subsequent to hydrogenation about 0-10% of the arene double bonds have been reduced, and at least about 90% of the conjugated diene double bonds have been reduced, (c) each A block having a number average molecular weight between about 3,000 and about 60,000 and each B block having a number average molecular weight between about 30,000 and about 300,000, (d) each B block comprises terminal regions adjacent to the A blocks that are rich in conjugated diene units and one or more regions not adjacent to the A blocks that are rich in mono alkenyl arene units, (e) the total amount of mono alkenyl arene in the hydrogenated block copolymer is about 5 percent weight to about 50 percent weight, and (f) the weight percent of mono alkenyl arene in each B block is between about 10 percent and about 75 percent. The thermoplastic polyurethane elastomer is present in the block copolymer in an amount from about 50 to about 95 percent by weight of a thermoplastic polyurethane elastomer.

Thermoplastic polyurethane block copolymer compositions

The present invention comprises a molding composition comprising at least about 70% wt. polypropylene or polypropylene random copolymer; up to about 30 wt. % of a block copolymer composition comprising at least one selectively hydrogenated block copolymer which substantially matches the index of refraction of the polypropylene or polypropylene random copolymer, and up to about 0.70% by wt. of a clarifying agent, wherein the weight % of the total blend is 100%. The present invention also may be a molded article produced from the molding composition. A molded article formed from such a composition at a thickness of 0.125 inches will have a haze of less than about 50% and an instrumented impact toughness of at least 100 inch-lbs at &#x2212;20&#xb0; C. to &#x2212;30&#xb0; C.

Growing community of inventors

Houston, TX, United States of America

Ruidong Ding