A bio-based polycarbonate ester resin is environment friendly by not containing a bisphenol, and exhibits excellent heat resistance, transparency, strength, hardness, dimensional stability and chemical resistance. Thus, the bio-based polycarbonate ester resin is suitable for use in an eyeglass frame. In addition, various colors may be painted and coated on during post-processing, a separate additive is not required during a molding process, and processing is undergone at a temperature lower than that for conventional plastic materials for an eyeglass frame, and thus manufacturing costs may be reduced.

A bio-based polycarbonate ester resin is environment friendly by not containing a bisphenol, and exhibits excellent heat resistance, transparency, strength, hardness, dimensional stability and chemical resistance. Thus, the bio-based polycarbonate ester resin is suitable for use in an eyeglass frame. In addition, various colors may be painted and coated on during post-processing, a separate additive is not required during a molding process, and processing is undergone at a temperature lower than that for conventional plastic materials for an eyeglass frame, and thus manufacturing costs may be reduced.

Release layers that include an oligomeric component comprising a unit of the Formula (I) are useful for releasably transferring components from one surface to another during manufacturing of microelectronic devices.

The present disclosure relates to block copolymers comprising, and methods of making thereof, a polycarbonate chain linked to a hydrophilic polymer. Such block copolymers may have the formula B-A-B, where A is a polycarbonate or polyethercarbonate chain and B is a polyether. Provided methods are useful in reducing the amount of waste generated from the synthesis of polycarbonates and provide improved thermal stability and high primary hydroxyl content. Provided block copolymers also have utility as additives in enhanced oil recovery methods, and foam polymer applications.

The present disclosure relates to block copolymers comprising, and methods of making thereof, a polycarbonate chain linked to a hydrophilic polymer. Such block copolymers may have the formula B-A-B, where A is a polycarbonate or polyethercarbonate chain and B is a polyether. Provided methods are useful in reducing the amount of waste generated from the synthesis of polycarbonates and provide improved thermal stability and high primary hydroxyl content. Provided block copolymers also have utility as additives in enhanced oil recovery methods, and foam polymer applications.

In an embodiment, a reactor for carrying out a melt transesterification reaction at a reactor temperature of 160 to 300° C. and a reactor pressure of 5 to 200 mbar, comprises a cylindrical tank comprising a top, a side, and a bottom, wherein the bottom is convex, extending away from the top; a stirring shaft disposed within the cylindrical tank along an axis thereof so that it is rotatable from outside of the cylindrical tank; a stirring blade extending from the stirring shaft in the cylindrical tank; a reactant solution inlet located on the bottom; and a reaction solution outlet located on the bottom. The reactor can be used for the polymerization of a polycarbonate oligomer.

A water-soluble polymer having an aliphatic polycarbonate backbone, a first carbonate monomer with at least one hydrophilic functionality, and a second carbonate monomer with at least one hydrophobic functionality is able to completely and quickly eliminate a virus from a human and/or animal cell. The at least one hydrophilic functionality is a sulfate, a sulfonate, a carboxylate, and/or a phosphate and the at least one hydrophobic functionality is an alkyl. The hydrophilic/hydrophobic functionalities of the polymer may be tuned to enhance the antiviral properties of the polymer and/or to decrease any cytotoxicity associated with the application of the polymer to a human and/or animal cell. The antiviral polymer is biocompatible and biodegradable.

A method for preparing polyether carbonate alcohols by attaching cyclic carbonate to an H-functional starter substance in the presence of a catalyst, characterized in that a tribasic alkali- or alkaline earth metal phosphate is used as the catalyst, the alkali metal being selected from potassium or cesium.

The present invention relates to a melt transesterification process for the production of (co)polycarbonates from diaryl carbonates and cycloalkylidene diphenols, which process comprises the addition of a monohydroxyaryl compound in an amount of 5.0 to 20.0 wt.-%, based on the total mass of the reaction mixture. The invention further relates to a (co)polycarbonate obtained by the process.

The invention relates to a process for preparing an aromatic carbonate, comprising reacting a dialkyl carbonate or an alkyl aryl carbonate with an aryl alcohol or an alkyl aryl carbonate, resulting in an aromatic carbonate which is an alkyl aryl carbonate or a diaryl carbonate, wherein a composition comprising a titanium or zirconium alkoxide or aryloxide, wherein the alkoxy group in the titanium or zirconium alkoxide is a group of formula R-0˜ wherein R is an alkyl group having 1 to 4 carbon atoms and the aryloxy group in the titanium or zirconium aryloxide is a group of formula Ar-0˜ wherein Ar is an aryl group having 6 to 12 carbon atoms, and wherein the composition additionally comprises 0.1 to 50 wt. % of an alcohol, based on the total weight of the composition, is mixed with an alcohol or an organic carbonate, and the mixture thus obtained is contacted with said dialkyl carbonate or alkyl aryl carbonate and aryl alcohol or alkyl aryl carbonate to catalyze the preparation of the aromatic carbonate. Further, the invention relates to a process for making a polycarbonate from the diaryl carbonate thus prepared.