Abstract: A thermoplastic composition comprises: a copolycarbonate comprising bisphenol A carbonate units and second carbonate units of the formula (I) and optionally, a bisphenol A homopolycarbonate; wherein the second carbonate units are present in an amount of 10 to 49 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate, the copolycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography, and the thermoplastic composition has a bisphenol A purity of at least 99.6%, or at least 99.7% as determined by high performance liquid chromatography. The thermoplastic composition has a Vicat B120 of 155° C. or higher; and an increase in yellowness index of less than 10 during 1000 hours of heat aging at 155° C.

Abstract: tic composition includes: a high heat polycarbonate comprising optional bisphenol A carbonate units and high heat carbonate units of the formula (1), (2), (3), or a combination thereof; optionally a bisphenol A homopolycarbonate; and 2 to 40 ppm of an organosulfonic stabilizer of the formula (a) wherein the high heat carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the high heat polycarbonate and the bisphenol A homopolycarbonate, and optionally the high heat polycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography; and the thermoplastic composition has: a Vicat B120 of 160° C.

Abstract: In an embodiment a method of purifying acetone, comprises directing a feed stream comprising greater than or equal to 97 wt % of acetone and 100 to 1,000 ppm of methanol to a separation column, both based on a total weight of the feed stream; separating the feed stream in the separation column that is operating at a pressure greater than or equal to 1 bar into an overhead stream and a purified acetone stream comprising less than or equal to 50 ppm of methanol based on a total weight of the purified acetone stream; and directing at least 80 wt % of the overhead stream into the separation column as a reconstituted stream and purging 1 to 20 wt % of the overhead stream as a purge stream.

Abstract: A lens containing a polycarbonate composition is disclosed. The polycarbonate composition includes a copolycarbonate having bisphenol A carbonate units and second carbonate units of the formula and 2 to 40 ppm of an organosulfonic stabilizer of the formula wherein the second carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate. The polycarbonate composition has: a Vicat B120 of 160° C. or higher measured according to ISO 306; and a yellowness index of less than 12, measured according to ASTM D1925.

Abstract: In an embodiment a method of purifying acetone, comprises directing a feed stream comprising greater than or equal to 97 wt % of acetone and 100 to 1,000 ppm of methanol to a separation column, both based on a total weight of the feed stream; separating the feed stream in the separation column that is operating at a pressure greater than or equal to 1 bar into an overhead stream and a purified acetone stream comprising less than or equal to 50 ppm of methanol based on a total weight of the purified acetone stream; and directing at least 80 wt % of the overhead stream into the separation column as a reconstituted stream and purging 1 to 20 wt % of the overhead stream as a purge stream.

Abstract: In an embodiment, a method of dewatering a wet polymer composition comprises introducing the wet polymer composition via a polymer feed location to a powder conveying section of an extruder; wherein the wet polymer composition comprises greater than or equal to 1 wt % of water based on the total weight of the wet polymer composition; venting the water through a conveying section vent to form a dry polymer composition; melt kneading the dry polymer composition in a melt kneading section of the extruder to form a polymer melt; conveying the polymer melt in a melt conveying section of the extruder; and adding an additive in one or both of the powder conveying section and the melt conveying section.

Abstract: A thermoplastic composition comprises: a copolycarbonate comprising bisphenol A carbonate units and second carbonate units of the formula (I); and 2 to 40 ppm of an organosulfonic stabilizer of the formula (II); wherein the second carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate, and optionally the copolycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography; and the thermoplastic composition has: a Vicat B120 of 160° C. or higher measured according to ISO 306; and a yellowness index of less than 12, measured according to ASTM D1925.

Abstract: A thermoplastic composition comprises: a copolycarbonate comprising bisphenol A carbonate units and second carbonate units of the formula and 2 to 40 ppm of an organosulfonic stabilizer of the formula wherein the second carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate, and optionally the copolycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography; and the thermoplastic composition has: a Vicat B120 of 160° C. or higher measured according to ISO 306; and a yellowness index of less than 12, measured according to ASTM D1925.

Abstract: In an embodiment, a catalyst comprises a porous carrier having 5 to 200 pores per 2.54 centimeters and a pore volume of at least 90 vol % based on the total volume of the porous carrier; wherein the porous carrier comprises one or both of carbon and a metal; and a sulfonated, cross-linked polystyrene located on at least part of a surface of the porous carrier.

Abstract: A thermoplastic composition comprises: a copolycarbonate comprising bisphenol A carbonate units and second carbonate units of the formula (I) and optionally, a bisphenol A homopolycarbonate; wherein the second carbonate units are present in an amount of 10 to 49 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate, the copolycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography, and the thermoplastic composition has a bisphenol A purity of at least 99.6%, or at least 99.7% as determined by high performance liquid chromatography. The thermoplastic composition has a Vicat B120 of 155° C. or higher; and an increase in yellowness index of less than 10 during 1000 hours of heat aging at 155° C.

Abstract: Polysiloxane-polycarbonates and improved methods for preparing the polysiloxane-polycarbonates are provided. Also provided are blend compositions including the polysiloxane-polycarbonates. The blend compositions can include one or more additional polymers. The blend compositions can include one or more additives. The blend compositions can be used to prepare articles of manufacture.

Abstract: tic composition includes: a high heat polycarbonate comprising optional bisphenol A carbonate units and high heat carbonate units of the formula (1), (2), (3), or a combination thereof; optionally a bisphenol A homopolycarbonate; and 2 to 40 ppm of an organosulfonic stabilizer of the formula (a) wherein the high heat carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the high heat polycarbonate and the bisphenol A homopolycarbonate, and optionally the high heat polycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography; and the thermoplastic composition has: a Vicat B120 of 160° C.

Abstract: A thermoplastic composition comprises: a copolycarbonate comprising bisphenol A carbonate units and second carbonate units of the formula (I); and 2 to 40 ppm of an organosulfonic stabilizer of the formula (II); wherein the second carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate, and optionally the copolycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography; and the thermoplastic composition has: a Vicat B120 of 160° C. or higher measured according to ISO 306; and a yellowness index of less than 12, measured according to ASTM D1925.

Abstract: A copolycarbonate lens formed from a polycarbonate composition comprising: a copolycarbonate comprising bisphenol A carbonate units and of phthalimide carbonate and optionally, a bisphenol A homopolycarbonate; wherein the second carbonate units are present in an amount of 18 to 35 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate, the copolycarbonate comprises less than 2 ppm by weight of each of an ion of lithium, sodium, potassium, calcium, magnesium, ammonium, chlorine, bromine, fluorine, nitrite, nitrate, phosphite, phosphate, sulfate, formate, acetate, citrate, oxalate, trimethylammonium, and triethylammonium, as measured by ion chromatography, and the polycarbonate composition has a bisphenol A purity of at least 99.7% as determined by high performance liquid chromatography. The polycarbonate composition has: a Vicat B120 of 155° C. or higher; and an increase in yellowness index of less than 10 during 1000 hours of heat aging at 155° C.

Abstract: A lens comprising a copolycarbonate comprising bisphenol A carbonate units and second carbonate units of the formula (I) and 2 to 40 ppm of an organosulfonic stabilizer of the formula (II), wherein the second carbonate units are present in an amount of 20 to 49 mol %, preferably 30 to 40 mol % based on the sum of the moles of the copolycarbonate and the bisphenol A homopolycarbonate; and the polycarbonate composition has: a Vicat B120 of 160° C. or higher measured according to ISO 306; and a yellowness index of less than 12, measured according to ASTM D1925.

Abstract: In an embodiment, a catalyst comprises a porous carrier having 5 to 200 pores per 2.54 centimeters and a pore volume of at least 90 vol % based on the total volume of the porous carrier; wherein the porous carrier comprises one or both of carbon and a metal; and a sulfonated, cross-linked polystyrene located on at least part of a surface of the porous carrier.

Abstract: In an embodiment, a method of producing a bisphenol comprises reacting a phenolic compound with a reactant comprising one or both of an aldehyde and a ketone in the presence of a catalyst system and methanol to produce the bisphenol; wherein the methanol is present in an amount of 250 to 5,000 ppm based on the total weight of the reactant; wherein the catalyst system comprises an ion-exchange resin comprising a plurality of sulfonic acid sites; and 5 to 35 mol % of an attached promoter molecule based on the total moles of the sulfonic acid sites in the catalyst system; and wherein the attached promoter molecule comprises at least two thiol groups per attached promoter molecule.

Abstract: In an embodiment, a method of dewatering a wet polymer composition comprises introducing the wet polymer composition via a polymer feed location to a powder conveying section of an extruder; wherein the wet polymer composition comprises greater than or equal to 1 wt % of water based on the total weight of the wet polymer composition; venting the water through a conveying section vent to form a dry polymer composition; melt kneading the dry polymer composition in a melt kneading section of the extruder to form a polymer melt; conveying the polymer melt in a melt conveying section of the extruder; and adding an additive in one or both of the powder conveying section and the melt conveying section.

Abstract: In an embodiment, a method of producing a bisphenol comprises reacting a phenolic compound with a reactant comprising one or both of an aldehyde and a ketone in the presence of a catalyst system and methanol to produce the bisphenol; wherein the methanol is present in an amount of 250 to 5,000 ppm based on the total weight of the reactant; wherein the catalyst system comprises an ion-exchange resin comprising a plurality of sulfonic acid sites; and 5 to 35 mol % of an attached promoter molecule based on the total moles of the sulfonic acid sites in the catalyst system; and wherein the attached promoter molecule comprises at least two thiol groups per attached promoter molecule.

Abstract: Polysiloxane-polycarbonates and improved methods for preparing the polysiloxane-polycarbonates are provided. Also provided are blend compositions including the polysiloxane-polycarbonates. The blend compositions can include one or more additional polymers. The blend compositions can include one or more additives. The blend compositions can be used to prepare articles of manufacture.