Sabic Global Technologies B.v.

Shpp Global Technologies B.v.

General Electric Company

Sabic Innovative Plastics IP B.v.

Gaurav Mediratta

Kapil Chandrakant Sheth

Hariharan Ramalingam

Gurunath Pozhal Vengu

Rajesh Chowdhury

Shivakumar Konda

Pradeep Jeevaji Nadkarni

Gautam Chatterjee

Gerrit De Wit

Veeraraghavan Srinivasan

Alvaro Carrillo

Venkata Rama Narayanan Ganapathy Bhotla

Salkod Parameshwar Mallika

Shubashree Swaminathan

Gheorghe Cojocariu

Chandrashekhar Lingannaiah

Radhakrishna Srinivasarao Arakali

Arun Sikder

Atul Pant

Gary Francis Smith

Chandra S Bajgur

Lohith Kenchaiah

Kenchaiah Lohith

Shantaram Suryakant Morye

Anup Krishnnan Appukuttan Pillai

Satish Chandra Pandey

Mukesh Agrawal

Shadaksharaswamy Puttamadappa

Ranjith Choorikkat

Sumi Dummyname

Deshmukh Shivajirao Sandesh

Niket Sharma

Shantaram Morye

Gary Smith

A process and system for the precipitation of poly(phenylene ether) is described. Precipitated poly(phenylene ether) obtained by the processes disclosed herein are in the form of poly(phenylene ether) particles having a bulk density of 150 to 500 kg/m, preferably 250 to 500 kg/m.

Process and apparatus for precipitation of poly (phenylene ether)

A functional phenylene ether oligomer of the structure wherein Q, Q, Q, Q, x, y, and R are as defined herein. A curable composition includes the functional phenylene ether oligomer, and a thermoset composition includes a cured product derived from the curable composition.

Functional phenylene ether oligomer, curable and thermoset compositions prepared therefrom

A copolymer having the structure (I) wherein Q, Q, Q, Q, m, and n are defined herein. The copolymer can be formed by oxidative copolymerization of 2,4,6-trimethyIresorcinoI with a monohydric phenol. Also describes are a composition comprising the copolymer and a solvent, and a composition comprising the copolymer and a thermosetting resin. 

Phenylene ether copolymer and compositions comprising same

A composition comprises, based on the total weight of the composition, 25 wt % to 50 wt % of a polyetherimide; and 50 wt % to 75 wt % of a polyphthalamide; wherein the composition has a number of drops to tracking at 250 volts of greater than or equal to 50 drops determined according to ASTM D-3638-85.

Electrical tracking resistance compositions, articles formed therefrom, and methods of manufacture thereof

A method for the manufacture of a 2-aryl-3,3-bis(hydroxyaryl)phthalimidine including heating a reaction mixture comprising a phenolphthalein compound and a primary arylamine in the presence of an acid catalyst, and a heterocyclic aromatic amine co-catalyst, to form the 2-aryl-3,3-bis(hydroxyaryl) is provided. Polymers including structural units derived from the 2-aryl-3,3-bis(hydroxyaryl)phthalimidine are provided. Methods for the manufacture of a polycarbonate, including manufacturing the 2-aryl-3,3-bis(hydroxyaryl)phthalimidine, and polymerizing the 2-aryl-3,3-bis(hydroxyaryl)phthalimidine in the presence of a carbonate source are provided.

Methods of manufacture of 2-aryl-3,3-bis(4-hydroxyaryl)phthalimidines, and polymers derived therefrom

A composition comprises, based on the total weight of the composition, 50 wt % to 90 wt % of a polyetherimide; and 10 wt % to 50 wt % of a filler comprising talc, titanium dioxide, zirconium oxide, neutral aluminum oxide, or a combination comprising at least one of the foregoing; wherein the composition has a number of drops to tracking at 250 volts of greater than or equal to 50 drops determined according to ASTM D-3638-85.

The disclosure concerns healable polycarbonate resins comprising at least about 5 mol % of disulfide units, articles comprising the healable polycarbonate resin, and methods of activating the healable polycarbonate resin by exposing the healable polycarbonate resin to heat or radiation.

Inherently healing polycarbonate resins

An improved method of manufacture of a bisphenol comprises heating a monohydric phenol to a first temperature sufficient to melt the monohydric phenol; adding a carbonyl compound to 2.0-3.0 molar equivalents, based on the moles of carbonyl compound, of the monohydric phenol in the presence of catalytic amounts of an organosulfonic acid catalyst and a reaction promoter at a second temperature sufficient to maintain unreacted monohydric phenol in a molten state; increasing the temperature to a third temperature higher than the second temperature, and mixing for a time sufficient to produce the bisphenol in a yield of 80 to 100%, based on the amount of carbonyl compound; wherein mineral acids, Lewis acids, and ion exchange resins are not used. The method is applicable to the manufacture of 2,2-bis(3,5-dimethyl-4-hydroxyphenyl)propane, a useful intermediate for the manufacture of bi-functional poly(phenylene ether)s.

Method of bisphenol manufacture

A composition comprises, based on the total weight of the composition, 45 wt % to 75 wt % of a polyetherimide; and 20 wt % to 45 wt % of talc; and 5 wt % to 15 wt % of a fluorinated polymer; wherein the composition has a number of drops to tracking at 250 volts of greater than or equal to 50 drops according to ASTM D-3638-85.

Methods for synthesizing and purifying 2-aryl-3,3-bis(4-hydroxyaryl)phthalimidine compounds are provided. The method includes heating a reaction mixture including a phenolphthalein, a primary aryl amine, and an acid catalyst to form a phthalimidine; precipitating the phthalimidine from the reaction mixture to provide a crude phthalimidine; providing a solution including the crude phthalimidine, an additive, and at least one solvent; contacting the solution with one or more purification agents to provide a treated solution; precipitating and recovering a phthalimidine adduct from the treated solution; and recovering a purified phthalimidine compound from the adduct.

Methods for purifying 2-aryl-3,3-bis(hydroxyaryl)phthalimidines

Disclosed herein is a polymer blend comprising a first polycarbonate comprising a first structural unit derived from a 2-aryl-3,3-bis(4-hydroxyaryl)phthalimidine and a second structural unit derived from a dihydroxy aromatic compound, wherein the second structural unit is not identical to the first structural unit, and a second polycarbonate comprising a structural unit derived from a dihydroxy aromatic compound, wherein the polymer blend has a glass transition temperature of 155 to 200&#xb0; C.; and wherein a test auricle having a thickness of 3.2 mm and molded from the blend has a haze of less than or equal to 3.0 measured in accordance with ASTM D1003-00. A method of making the polymer blend, and articles prepared from the blend, are also disclosed.

High heat polycarbonates, methods of making, and articles formed therefrom

Novel polyester composition comprising a polyester, wherein said polyester comprises structural units derived from substituted or unsubstituted diacid or diester, a substituted or unsubstituted diol; a phosphorus containing compound and at least one selected from a stabilizer and an organic compound comprising at least one functional group is been disclosed. In addition methods for the preparation of the polyester composition and articles derived from said composition is disclosed.

Halogen-free flame retardant polyester

A flame retardant thermoplastic resin composition comprises a thermoplastic resin comprising a polyphenylene ether resin, a high impact polystyrene resin or an acrylontrile-butadiene-styrene resin; an organo phosphate compound in an amount less than or equal to about 20 parts by weight for every 100 parts by weight of the thermoplastic resin; and a polyhydric alcohol compound in an amount of about 0.5 to about 5.0 parts for every 100 parts by weight of the thermoplastic resin. A method for the manufacture of the thermoplastic resin composition is also disclosed. The thermoplastic resin composition exhibits high flow characteristics and improved impact strength while providing effective flame retardance.

Growing community of inventors

Bengaluru, India

Gaurav Mediratta