Abstract: Copolycarbonates containing such structural units as birefringence-reducing or "soft block" units are prepared by conducting a reaction, such as melt polymerization or equilibration, between a precursor polycarbonate and a monomer, polycarbonate oligomer or high molecular weight polycarbonate which is a source of other structural units. The crystallinity of the resulting precursor copolycarbonate or one of the reagents employed in its preparation is enhanced and the precursor copolycarbonate is subjected to solid state polymerization.

Abstract: Copolycarbonates comprise structural units derived from a bisphenol such as bisphenol A, a spiro(bis)indane bisphenol such as 6,6'-dihdyroxy-3,3,3',3'-tetramethyl-1,1'-spiro(bis)indane and a polyoxyalkylene glycol such as polyethylene glycol. These copolycarbonates have high processability and are expected to have low birefringence. They are useful for the fabrication of optical disks.

Abstract: Polycarbonates are recycled without the need for chemical modification by dissolution in a solvent followed by removal of any insoluble materials and precipitation by addition of a non-solvent. The precipitation step may be followed by solid state polymerization of the recycled polycarbonate. Particularly when solid state polymerization is to be performed, the use of a combination of solvent and non-solvent which produces a crystalline intermediate is performed, and use of a modifying reagent increasing the hydroxy end group concentration of the polycarbonate may be advantageous.

Abstract: A method for determining the effective level of catalyst for the preparation of a polycarbonate polymer by a transesterification reaction is disclosed. The method involves measurement of the leaving group by-product (usually phenol) produced in a test reaction between an aromatic dihydroxy compound and a carbonic acid diester, in the presence of a known amount of transesterification catalyst. The by-product production values can be compared with by-product reference values to calculate the effective level of catalyst. This data can be used to efficiently control catalytic activity in a production scale reaction for producing polycarbonate polymer.

Abstract: Solid state polycarbonate formation comprises an initial step of converting a precursor polycarbonate to an enhanced crystallinity precursor polycarbonate and a second step of polymerizing said enhanced crystallinity precursor polycarbonate in the solid state. Several options are employed. These include modifying the precursor polycarbonate by contact with a dihydroxy compound or diaryl carbonate, conversion of the precursor polycarbonate to the enhanced crystallinity polymer by contact with at least one compound selected from the group consisting of alkali metal hydroxides, tetraalkylammonium hydroxides, tetraalkylammonium carboxylates, tetraalkylphosphonium hydroxides and tetraalkylphosphonium carboxylates, and conducting the solid state polymerization in the presence of a catalytic amount of at least one tetralkylammonium or tetraalkylphosphonium carboxylate. The preferred tetralkylammonium compounds are tetramethylammonium maleate and tetramethylammonium hydroxide.