Abstract: A method for reducing the concentration of amines in a wash liquid stream exiting a wash section in an acid gas scrubbing process includes introducing the wash liquid stream exiting the wash section of the acid gas scrubbing process to an adsorbent material, wherein the wash liquid stream has a first concentration of amines. The wash liquid stream having the first concentration of amines is flowed through the adsorbent material, and the adsorbent material retains at least a portion of the amines thereby providing a wash liquid stream having a second, reduced concentration of amines. The wash stream with reduced concentration of amines is recycled back to the wash section to remove amines more effectively from the acid gas being scrubbed. The adsorbent material can be regenerated for reuse. Amine recovered from the regenerated adsorbent material can be recycled to the process for reuse.

Abstract: A non-aqueous solvent system configured to remove acidic gas from a gas stream comprises a solution formed of a chemical absorption component and a physical absorption component. The chemical absorption component includes a nitrogenous base, wherein the nitrogenous base has a structure such that it reacts with a portion of the acidic gas. The physical absorption component includes an organic diluent that is non-reactive with the acidic gas and that has a structure such that it absorbs a portion of the acidic gas at a pressure above atmospheric pressure. The solvent system has a solubility with water of less than about 10 g of solvent per 100 mL of water.

Abstract: The present disclosure provides mixed molybdenum oxide catalysts, methods for preparing epoxides from olefins and CO2 using them, and methods of making the mixed molybdenum oxide catalysts by impregnation or co-precipitation. In a preferred embodiment, the mixed molybdenum oxide catalysts are silver/molybdenum oxide catalysts, ruthenium/molybdenum oxide catalysts, or a combination thereof.

Abstract: The present disclosure provides mixed molybdenum oxide catalysts, methods for preparing epoxides from olefins and CO2 using them, and methods of making the mixed molybdenum oxide catalysts by impregnation or co-precipitation. In a preferred embodiment, the mixed molybdenum oxide catalysts are silver/molybdenum oxide catalysts, ruthenium/molybdenum oxide catalysts, or a combination thereof.

Abstract: The invention relates to the use of and method of forming Low Temperature Cofired Ceramic (LTCC) circuits for high frequency applications. Furthermore, the invention relates to the novel LTCC thick film compositions and the structure itself.

Abstract: A method for the production of a polyestercarbonate comprises (i) providing at least one dihydroxyaromatic compound (ii) providing a carbonate precursor and (iii) providing at least one solid, biosynthetically derived, aliphatic alpha-omega dicarboxylic acid having about 10 to about 22 carbon atoms and having a nitrogen content of not more than about 55 ppm, and reacting interfacially in the presence of a base said dihydroxyaromatic compound, said carbonate precursor and said dicarboxylic acid.

Abstract: Aliphatic tricarboxylic acids, as exemplified by 9-carboxy-1,18-octadecanedioic acid, may be prepared by the biotransformation of an olefinic monocarboxylic acid such as oleic acid to the corresponding olefinic dicarboxylic acid, preferably 1,18-octadec-9-enedioic acid, in the presence of a strain of yeast, such as a strain of Candida tropicalis, followed by the carboxylation of the olefinic dicarboxylic acid by reaction with carbon monoxide and water in the presence of a catalyst. The product tricarboxylic acids are useful as branching agents for polycarbonates.

Abstract: Aliphatic tricarboxylic acids, as exemplified by 9-carboxy-1,18-octadecanedioic acid, may be prepared by the biotransformation of an olefinic monocarboxylic acid such as oleic acid to the corresponding olefinic dicarboxylic acid, preferably 1,18-octadec-9-enedioic acid, in the presence of a strain of yeast, such as a strain of Candida tropicalis, followed by the carboxylation of the olefinic dicarboxylic acid by reaction with carbon monoxide and water in the presence of a catalyst. The product tricarboxylic acids are useful as branching agents for polycarbonates.

Abstract: Aliphatic tricarboxylic acids, as exemplified by 9-carboxy-1,18-octadecanedioic acid, may be prepared by the biotransformation of an olefinic monocarboxylic acid such as oleic acid to the corresponding olefinic dicarboxylic acid, preferably 1,18-octadec-9-enedioic acid, in the presence of a strain of yeast, such as a strain of Candida tropicalis, followed by the carboxylation of the olefinic dicarboxylic acid by reaction with carbon monoxide and water in the presence of a catalyst. The product tricarboxylic acids are useful as branching agents for polycarbonates.

Abstract: Copolyestercarbonates comprising carbonate structural units derived from at least one dihydroxyaromatic compound, preferably bisphenol A, and ester units derived from a dihydroxyaromatic compound and a composition comprising at least one C36 dimer acid may be prepared by an interfacial phosgenation method conducted at a pH in the range of about 9-11. The copolyestercarbonates have properties which are often superior to those of corresponding polymers prepared, for example, from dodecanedioic acid.

Abstract: Copolyestercarbonates comprising carbonate structural units derived from at least one dihydroxyaromatic compound, preferably bisphenol A, and ester units derived from a dihydroxyaromatic compound and a composition comprising at least one C36 dimer acid may be prepared by an interfacial phosgenation method conducted at a pH in the range of about 9-11. The copolyestercarbonates have properties which are often superior to those of corresponding polymers prepared, for example, from dodecanedioic acid.

Abstract: A method for preparing a polyestercarbonate copolymer using solid state polymerization and polyestercarbonates prepared thereby is described. The method comprises preparing a mixture comprising partially crystalline bisphenol A polycarbonate oligomer and hydroxy acids, aliphatic diacids, cycloaliphatic diacids, aromatic diacids or aromatic triacids and subjecting that mixture to solid state polymerization to afford a polyestercarbonate copolymer.

Abstract: The present invention related to a method for preparing a polyestercarbonate, the method comprising: a) reacting a dihydric phenol and a diacid having from 12 to about 30 carbon atoms in the presence of an effective amount of carbonate precursor, thereby forming a reaction mixture, wherein the pH of the reaction mixture is maintained in an initial pH range of from about 8.5 to about 9.5 for about 50% to about 95% of the total carbonate precursor addition, and a second pH range of from about 10 to about 12 for the remainder of the carbonate precursor addition.

Abstract: This invention relates to polyestercarbonates comprising residues of at least one branched aliphatic dicarboxylic acid, and methods for preparation of polyestercarbonates comprising residues of at least one branched aliphatic dicarboxylic acid. This invention further relates to articles and methods of making articles from the polyestercarbonates.

Abstract: This invention provides a low-cost method of producing .alpha.,.omega.-alkanedicarboxylic acids. Particular bioconversion conditions result in highly efficient conversion of fatty acid, fatty acid ester, or alkane substrates to diacids. Candida tropicalis AR40 or similar yeast strains are grown in a medium containing a carbon source and a nitrogen source at a temperature of 31.degree. C. to 38.degree. C., while additional carbon source is continuously added, until maximum cell growth is attained. Within 0-3 hours of this point, substrate is added to the culture to initiate conversion. An .alpha.,.omega.-alkanedicarboxylic acid made according to this method is also provided.

Abstract: This invention describes a low cost biofermentation medium, and an economical method using the medium, for the manufacture of .alpha., .omega.-alkanedicarboxylic acids. The invention provides a biofermentation medium and a method of bioproduction for these important diacids which makes their large scale commercial production economically feasible using a biocatalyst. This method of production obviates the need for chemical synthesis using expensive starting materials from fossil fuels, and does not generate a costly hazardous waste stream.