Abstract: The present invention relates to a method for the manufacture of a (co)polycarbonate comprising reacting tetrabromo bisphenol A and optionally one or more bisphenol comonomer(s) with phosgene wherein the tetrabromo bisphenol A contains an amount of tetrabromo bisphenol A dimer of at most 3.0 wt.% based on the weight of the tetrabromo bisphenol A, determined after heat treating the tetrabromo bisphenol A at a temperature of 260° C. for a period of 15 minutes.

Abstract: A copolycarbonate includes 0.005-0.1 mole percent of sulfur-containing carbonate units derived from a sulfur-containing bisphenol monomer, 2-95 mole percent of high heat carbonate units derived from a high heat aromatic dihydroxy monomer, and 5-98 mole percent of a low heat carbonate units derived from a low heat aromatic monomer, each based on the sum of the moles of the carbonate units; and optionally, thioether carbonyl endcaps of the formula —C(?O)-L-S—R, wherein L is a C1-12 aliphatic or aromatic linking group and R is a C1-20 alkyl, C6-18 aryl, or C7-24 arylalkylene; wherein the sulfur content of the high heat copolycarbonate in the absence of the thioether endcaps is from 5-20 parts per million by weight.

Abstract: A composite medium for collecting mineral particles in an aqueous slurry has a polymer substrate deposited or penetrated with an inorganic material and further coated with a hydrophobic material. The hydrophobic material can be a hydrophobic silane or a hydrophobic polymer such as polysiloxane. Alternatively, the inorganic material deposited substrate is first reacted with a reactive silane and then coated with a hydrophobic polymer. The polymer substrate can be in the form of a spherical bead, a small cube, a filter or a conveyor.

Abstract: A copolycarbonate included 2-95 mole percent of high heat carbonate units derived from a high heat aromatic dihydroxy monomer, wherein a polycarbonate homopolymer derived from the high heat aromatic dihydroxy monomer has a glass transition temperature of 175-330 C determined by differential scanning calorimetry as per ASTM D3418 with a 20 C/min heating rate, and 5-98 mole percent of a low heat carbonate units derived from a low heat aromatic monomer, wherein a polycarbonate homopolymer derived from the low heat aromatic monomer has a glass transition temperature of less than 170 C determined by differential scanning calorimetry as per ASTM D3418 with a 20 C/min heating rate, each based on the sum of the moles of the carbonate units; and a sulfur-containing stabilizer compound, wherein the sulfur-containing stabilizer compound is a thioether carboxy compound, a thioether dicarboxy compound, a thioether ester compound, or a combination thereof, wherein the sulfur-containing stabilizer compound is present in an

Abstract: A copolycarbonate optical article comprises a polycarbonate composition including: a copolycarbonate having: 2 to 60 mol % of phthalimidine carbonate units, 2 to 90 mol % of high heat carbonate units, and optionally 2 to 60 mol % of bisphenol A carbonate units. The copolycarbonate has less than 100 ppm of each of phthalimidine, high heat bisphenol, and bisphenol A monomers, and less than 5 ppm of various ions, and is prepared from monomers each having a purity of at least 99.6%. The polycarbonate composition has a glass transition temperature of 200° C. to and a yellowness index of less than 30.

Abstract: A copolycarbonate optical article comprises a polycarbonate composition including: a copolycarbonate having: 2 to 60 mol % of phthalimidine carbonate units, 2 to 90 mol % of high heat carbonate units, and optionally 2 to 60 mol % of bisphenol A carbonate units. The copolycarbonate has less than 100 ppm of each of phthalimidine, high heat bisphenol, and bisphenol A monomers, and less than 5 ppm of various ions, and is prepared from monomers each having a purity of at least 99.6%. The polycarbonate composition has a glass transition temperature of 200° C. to and a yellowness index of less than 30.

Abstract: A copolycarbonate includes 0.005-0.1 mole percent of sulfur-containing carbonate units derived from a sulfur-containing bisphenol monomer, 2-95 mole percent of high heat carbonate units derived from a high heat aromatic dihydroxy monomer, and 5-98 mole percent of a low heat carbonate units derived from a low heat aromatic monomer, each based on the sum of the moles of the carbonate units; and optionally, thioether carbonyl endcaps of the formula —C(?O)-L-S—R, wherein L is a C1-12 aliphatic or aromatic linking group and R is a C1-20 alkyl, C6-18 aryl, or C7-24 arylalkylene; wherein the sulfur content of the high heat copolycarbonate in the absence of the thioether endcaps is from 5-20 parts per million by weight.

Abstract: An endcapped polycarbonate, comprising thioether carbonyl endcaps of the formula wherein L is a C1-12 aliphatic or aromatic linking group, and R is a C1-20 alkyl, C6-18 aryl, or C7-24 arylalkylene.

Abstract: A phosphinate copolycarbonate having units of the formula (1) wherein each Ra is independently a halogen atom, C1-10 alkyl, C1-10 haloalkyl, C1-12 alkoxy, C6-10 aryl, or C6-12 haloaryl, each Xa is as defined herein, Re and Rf are independently a halogen atom, C1-10 alkyl, C1-10 haloalkyl, C1-10 alkoxy, C1-10 haloalkoxy, C2-10 alkenyl, or C3-10 cycloalkyl, each Rg is a substituted or unsubstituted C6-18 aryl, C1-10 alkyl, C1-10 haloalkyl, C1-10 alkoxy, C1-10 haloalkoxy, C2-10 alkenyl, C3-10 cycloalkyl, C6-10 aryl, or C6-12 haloaryl, Ara and Arb are each independently the same or different C6-18 aryl, a, e, and f are each independently 0 to 4, or 0 to 2 or 0, c is 0 or 1, and x and y represent the molar ratio of each unit in the phosphinate copolycarbonate, and are 0.5:99.5 to 99.5:0.5, or 1:99 to 99:1, or 10:90 to 90:10, or 20:80 to 80:20.

Abstract: Methods for screening molecules or moieties for their ability to crosslink are disclosed. An aromatic carbonate, aromatic ester, or aliphatic ester group is attached to the molecule to mimic the presence of a polymer. A solution of the modified molecule is irradiated, and the first-order kinetic rate constant is measured. If the rate constant is high enough or a threshold amount of the molecule is consumed, a polymer is synthesized using the molecule/moiety as an endcap or co-monomer. The polymer is irradiated, and the increase in crosslink density and the gel formation percentage are determined. These parameters, if high enough, indicate the suitability of the molecule/moiety to act as a crosslinking agent, particularly for polycarbonates. Alternatively, the molecule/moiety may be identified as suitable solely by its first-order kinetic rate constant.

Abstract: Methods for screening molecules or moieties for their ability to crosslink are disclosed. An aromatic carbonate, aromatic ester, or aliphatic ester group is attached to the molecule to mimic the presence of a polymer. A solution of the modified molecule is irradiated, and the first-order kinetic rate constant is measured. If the rate constant is high enough or a threshold amount of the molecule is consumed, a polymer is synthesized using the molecule/moiety as an endcap or co-monomer. The polymer is irradiated, and the increase in crosslink density and the gel formation percentage are determined. These parameters, if high enough, indicate the suitability of the molecule/moiety to act as a crosslinking agent, particularly for polycarbonates. Alternatively, the molecule/moiety may be identified as suitable solely by its first-order kinetic rate constant.

Abstract: Photoactive additives are disclosed. The additive includes a benzophenone having at least one substituent that comprises a divalent linker and a linking group, wherein the linking group is a carboxyl group, ester group, or acid halide group. The additive can be a polymer, an oligomer, or a compound. When added to a base polymeric resin, the photoactive additive permits crosslinking upon exposure to ultraviolet light.

Abstract: Photoactive additives are disclosed. The additive includes a benzophenone having at least one substituent that comprises a divalent linker and a linking group, wherein the linking group is a carboxyl group, ester group, or acid halide group. The additive can be a polymer, an oligomer, or a compound. When added to a base polymeric resin, the photoactive additive permits crosslinking upon exposure to ultraviolet light.