Patent application number | Description | Published |
20090043070 | COPOLYCARRBONATE-POLYESTERS, METHODS OF MANUFACTURE, AND USES THEREOF - A copolycarbonate-polyester, comprising units of formula | 02-12-2009 |
20090326149 | BRANCHED POLYCARBONATES AND PROCESSES FOR PRODUCING THE SAME - Methods for making a branched polycarbonate are disclosed. An interfacial mixture comprising water, a substantially water-immiscible organic solvent, a dihydroxy compound, a polyhydric branching agent, an endcapping agent, a catalyst, and a base is formed. The base and the branching agent are dissolved in the mixture before the dihydroxy compound is added, and the interfacial mixture has a basic pH. The mixture is reacted by adding a carbonate precursor to the mixture while maintaining the pH between about 8 and about 10 to form the branched polycarbonate. The resulting branched polycarbonates may contain more than 1.5 mole % of the THPE; have residual chloride content of 20 ppm or less; and a weight average molecular weight of about 55,000 or less. They may also be highly transparent. | 12-31-2009 |
20090326183 | BRANCHED POLYCARBONATE-POLYSILOXANE COPOLYMERS AND PROCESSES FOR PRODUCING THE SAME - Methods for making a branched polycarbonate-polysiloxane copolymer are provided. An interfacial mixture comprising water, an organic solvent, a polyhydric branching agent, a non-siloxane-containing dihydroxy compound, an endcapping agent, a phase transfer catalyst, and a base is formed. The base and the branching agent are dissolved in the mixture before the non-siloxane-containing dihydroxy compound is added and the interfacial mixture has a basic pH. A first carbonate precursor is added to the interfacial mixture while maintaining the pH at from about 3 to about 9 to form a branched polycarbonate mixture. Next, the pH is increased to from about 8 to about 13 and a siloxane oligomer is added to the branched polycarbonate mixture. The branched polycarbonate mixture is then reacted to form the branched polycarbonate-polysiloxane copolymer. The resulting branched copolymer contains 20 ppm or less of residual chloride, is transparent, has improved flow properties, and has good flame retardance at thin wall thicknesses. | 12-31-2009 |
20100152406 | BPA and Polycarbonate Made from Renewable Materials - Bio-derived bisphenol A is made by combining bio-derived phenol and/or bio-derived acetone in the presence of a catalyst, The phenol or the acetone or both contain at least 0.5%, for example at least 1 weight % of bio-derived impurities. In the case of bio-derived phenol, these impurities may include one or more of 2-methylbenzofuran, 2-methoxyphenol, 2-methylphenol, 4-methylphenol (para-cresol) or 2-methoxy-4-methylphenol. In the case of acetone, the impurity may be ethanol, mesityl acetone and/or diacetone alcohol. This bio-derived BPA can be used in the production of polycarbonates with less fossil fuel-based carbon content. | 06-17-2010 |
20100286358 | COPOLYCARRBONATE-POLYESTERS, METHODS OF MANUFACTURE, AND USES THEREOF - A copolycarbonate-polyester, comprising units of formula | 11-11-2010 |
20130053487 | POLYCARBONATE COMPOSITIONS AND METHODS FOR THE MANUFACTURE AND USE THEREOF - This disclosure relates generally to polycarbonate compositions whose hydrolysis products and residual monomer content, if any, exhibit little or no estradiol binding activity. Also disclosed are methods for making the disclosed polycarbonates and articles of manufacture comprising the disclosed polycarbonates. | 02-28-2013 |
20130053489 | POLYETHERIMIDE COMPOSITIONS AND METHODS FOR THE MANUFACTURE AND USE THEREOF - This disclosure relates to polyetherimide compositions whose residual phenolic monomers exhibit little or no estradiol binding activity. Also disclosed are methods for making the disclosed polyetherimides and articles of manufacture comprising the disclosed polyetherimides. | 02-28-2013 |
20140039102 | POLYSULFONE COMPOSITIONS AND METHODS FOR THE MANUFACTURE AND USE THEREOF - This disclosure relates generally to polysulfone compositions whose residual phenolic monomers or phenolic degradation products exhibit little or no estradiol binding activity. Also disclosed are methods for making the disclosed polysulfones and articles of manufacture comprising the disclosed polysulfones. | 02-06-2014 |