Abstract: Provided are a polyester polymerization catalyst with which the generation of foreign materials caused by the catalyst or mold pollution at the time of molding are reduced and polyesters having remarkably superior thermal stability and color tone can be obtained. Provided is a polyester polymerization catalyst produced by the reaction of a titanium compound and a mannitol in a molar ratio of titanium atom to mannitol of from 1:1 to 1:3. A method for producing a polyester employs the polyester polymerization catalyst.
Type:
Grant
Filed:
August 18, 2009
Date of Patent:
August 26, 2014
Assignee:
Toray Industries, Inc.
Inventors:
Yoichiro Tanaka, Eri Hatano, Keisuke Honda
Abstract: A method for making polyethylene terephthalate resin in which a titanium-nitride polycondensation catalyst is introduced during the initial stages of esterification or transesterification. The titanium-nitride polycondensation catalyst may be added to a mixture containing a terephthalate component and a diol component during the formation of a polyethylene terephthalate precursor. Subsequent polycondensation of the polyethylene terephthalate precursor forms a polyethylene terephthalate polymer.
Abstract: The invention relates to an improved linear microdialysis probe comprising a continuous length of flexible tubing (1) having at least one window (4) formed therein, said window covering at least one part of the circumference of the tubing, while the remaining part forms at least one unbroken connection between a first end of said tubing and a second end of said tubing, said ends adapted to be attached to an inlet for perfusion liquid and the other end forming an outlet for the dialysate, said at least one window (4) exposing a tubular semipermeable membrane (2).
Type:
Grant
Filed:
December 21, 2006
Date of Patent:
July 15, 2014
Assignee:
TORAY Industries, Inc.
Inventors:
Hua Qi, Keisuke Honda, Kunihiro Morimoto, Jun Sakamoto, Hiroji Kojima
Abstract: Disclosed are processes to prepare monocarboxylic acid esters (mono- and/or diesters) of polytrimethylene ether glycol that are substantially free of residues from the catalyst used to produce the polytrimethylene ether glycol esters, as well as methods for their preparation and end uses thereof. The esters, such as the bis-2-ethylhexanoate esters, have uses as functional fluids.
Type:
Grant
Filed:
June 23, 2010
Date of Patent:
June 24, 2014
Assignee:
E I du Pont de Nemours and Company
Inventors:
Hari Babu Sunkara, Raja Hari Poladi, Gyorgyi Fenyvesi
Abstract: Provided is a dehydroabietic acid polymer including a skeleton of the following formula (A) as a repeating unit: wherein L represents a divalent organic group. Methods for producing the dehydroabietic acid polymer are also provided. The dehydroabietic acid polymer has high resistance against moisture and water and high impact resistance. The dehydroabietic acid polymer can also be produced from a rosin-derived natural product.
Abstract: A method for preventing the formation of gas hydrates in an aqueous phase by adding esters of pyroglutamic acid in the quantities of from 0.01 to 2% by weight. The esters of pyroglutamic acid produced by esterifying at least one alcohols, comprising from 1 to 100 hydroxyl groups with pyroglutamic acid and/or glutamic acid, wherein the alcohol has no more than one ester group or no more than one carboxylic acid group.
Abstract: Bioresorbable or biodegradable polymers formed from the monomers including sulphonyl diphenol, hydroxybenzoic acid and dicarboxylic acid. The dicarboxylic acid can include aliphatic dicarboxylic acid or a mixture of aliphatic dicarboxylic acid and aromatic dicarboxylic acid. Between 25 and 85 molar percent of the polymer is formed from the hydroxybenzoic acid, between 7.5 and 37.5 molar percent of the polymer is formed from the sulphonyl diphenol, and between 7.5 and 37.5 molar percent of the polymer is formed from the dicarboxylic acid. Polymers can be used for manufacturing fibers and composite devices.
Abstract: The composition of a homopolymer of (phosphonyl) aromatic diester compound using a catalyst and a glycol is provided. Further, the composition of a copolymer of the (phosphonyl) aromatic diester compound using a catalyst, a glycol and a second diester is provided. These polymers find application as flame retardants during synthesis of various polymeric materials.
Type:
Grant
Filed:
December 8, 2011
Date of Patent:
May 13, 2014
Assignee:
E I du Pont de Nemours and Company
Inventors:
Neville Everton Drysdale, Fredrik Nederberg
Abstract: Deep-drawn membranes formed of polyester or polycarbonate films, comprising units of Formula (I) and (II), useful for acoustic signal converters as microphones and speakers. The film can be produced by thermoplastic processes or solvent cast processes.
Type:
Grant
Filed:
January 28, 2010
Date of Patent:
April 15, 2014
Assignee:
tesa SE
Inventors:
Kerstin Metzler, Bernhard Müssig, Frank Virus
Abstract: A polyester resin having a diol unit containing a unit derived from ethylene glycol and a unit derived from a diol represented by the following formula (I), and a dicarboxylic acid unit containing a unit derived from an aromatic dicarboxylic acid in an amount of 50 mol % or more; wherein the entire diol unit contains the unit derived from ethylene glycol in an amount of 40 to 99 mol %, and the unit derived from a diol represented by formula (I) in an amount of 1 to 60 mol %: wherein A represents an aromatic ring selected from the group consisting of benzene, naphthalene, anthracene, phenanthrene and pyrene; R1 represents a C1 to C12 alkyl group, a substituted or unsubstituted C6 to C12 aryl group or a halogen atom; n represents an integer of 0 to 4; and when plural R1s are present, R1s may be the same as or different from each other.
Type:
Grant
Filed:
December 24, 2010
Date of Patent:
March 18, 2014
Assignee:
Mitsubishi Gas Chemical Company, Inc.
Inventors:
Takuya Minezaki, Takeshi Hirokane, Dai Oguro
Abstract: In the production of an aliphatic polyester by ring-opening polymerization of a cyclic ester, at least a latter period of polymerization is proceeded with by way of solid-phase polymerization, and the resultant aliphatic polyester is subjected to removal of residual cyclic ester. As a result, an aliphatic polyester with a minimized content of residual monomer is obtained.
Abstract: A manufacturing method of polyethylene terephthalate including a step of melt polycondensation in presence of polycondensation catalyst represented by general Formula (I), wherein R1 represents an alkyl group having from 2 to 12 carbon atoms, and melt polycondensed polyethylene terephthalate has an intrinsic viscosity of from 0.48 to 0.53 dL/g and a terminal carboxyl number of from 14 to 22 mmol/kg; and a step of solid phase polycondensation to obtain solid phase polycondensed polyethylene terephthalate having an intrinsic viscosity of from 0.70 to 0.86 dL/g, and a terminal carboxyl number of less than 15 mmol/kg, followed by a step of applying an aqueous solution of at least one salt selected from the group consisting of acetate, carbonate, and sulfate of sodium, potassium, or cesium to the solid phase polycondensed polyethylene terephthalate, and then drying the polyethylene terephthalate, wherein the final content of sodium, potassium or cesium atom in dried polyethylene terephthalate is from 2 to 25 ppm.
Abstract: The present invention is an aliphatic polyester resin in which a polyhydroxy acid skeleton is a main component, manufactured using a polymerization catalyst, characterized in that a specific organophosphorus compound is copolymerized in the resin. Activity of the polymerization catalyst contained in the aliphatic polyester resin of the present invention after the polymerization is well lowered and a lactide is hardly produced even by heating after the polymerization or after the manufacture.
Abstract: A method for producing a binder resin comprises polycondensing a polycondensable monomer by using a polycondensation catalyst that comprises: at least one of compounds of formula (I) or (II); and at least one of compounds represented of formula (III) or (IV), wherein weight ratio of total amount of the compounds of formula (I) or (II) to total amount of the compounds of formula (III) or (IV) is from 5:95 to 95:5: wherein R1 represents a C8-C20 straight-chain alkyl group; R2 represents a monovalent organic group; and number n of substituents R2 represents an integer of from 0 to 4; R3—SO3H??(II) wherein R3 represents a C8-C20 straight-chain alkyl group; wherein R4 represents a C8-C20 branched alkyl group; R5 represents a monovalent organic group; and number m of substituents R5 represents an integer of from 0 to 4; and R6—SO3H??(IV) wherein R6 represents a C8-C20 branched alkyl group.
Abstract: A manufacturing method of polyethylene terephthalate including a step of melt polycondensation in presence of polycondensation catalyst represented by general Formula (I), wherein R1 represents an alkyl group having from 2 to 12 carbon atoms, and melt polycondensed polyethylene terephthalate has an intrinsic viscosity of from 0.48 to 0.53 dL/g and a terminal carboxyl number of from 14 to 22 mmol/kg; and a step of solid phase polycondensation to obtain solid phase polycondensed polyethylene terephthalate having an intrinsic viscosity of from 0.70 to 0.86 dL/g, and a terminal carboxyl number of less than 15 mmol/kg, followed by a step of applying an aqueous solution of at least one salt selected from the group consisting of acetate, carbonate, and sulfate of sodium, potassium, or cesium to the solid phase polycondensed polyethylene terephthalate, and then drying the polyethylene terephthalate, wherein the final content of sodium, potassium or cesium atom in dried polyethylene terephthalate is from 2 to 25 ppm.
Abstract: A conjugate of a modified randomly branched asymmetric polymer without a core and a member of a binding pair is described. The modified randomly branched asymmetric polymer can contain chain branches, terminal branches or both. The modified randomly branched asymmetric polymer can contain random asymmetric branches or random asymmetric junctions. The binding pair can be an antibody, antigen or a ligand.
Abstract: A conjugate of a modified randomly branched asymmetric polymer without a core and a member of a binding pair is described. The modified randomly branched asymmetric polymer can contain chain branches, terminal branches or both. The modified randomly branched asymmetric polymer can contain random asymmetric branches or random asymmetric junctions. The binding pair can be an antibody, antigen or a ligand. The conjugate includes a drug.
Abstract: A sulfopolyester containing residues of 2,2,4,4-tetralkylcyclobutane-1,3-diol such as 2,2,4,4-tetramethylcyclobutane-1,3-diol is highly dispersible in water. This allows one to reduce the content of sulfonate groups or reduce the amount of ethylene glycol or other hydrophilic glycols to retain good water resistance in cured coatings. The sulfopolyester may also be a reaction product of a 2,2,4,4-tetralkylcyclobutane-1,3-diol along with 1,4-cyclohexanedimethanol, neopentyl glycol, or a mixture thereof with an acid component. Coating compositions may also contain these sulfopolyesters along with water and a polymer resin.
Abstract: A process for producing an aliphatic polyester through ring-opening polymerization of a cyclic ester, wherein a partial polymer in a molten state is continuously introduced into a twin-screw stirring device to continuously obtain a partial polymer in a solid pulverized state, the partial polymer is subjected to solid-phase polymerization, and the resultant polymer is melt-kneaded together with a thermal stabilizer to be formed into pellets. As a result, an aliphatic polyester of a high molecular weight and with little discoloration is produced efficiently.
Abstract: The present invention is a high modulus bio-based polymer plastic composition or mixture and methods of preparing the same. The composition is formed from the reaction of a bio-based epoxidized triglyceride oil, an energy activated catalyst and a bio-based non-aromatic cross-linking compound to form a structural polymer plastic. The bio-based epoxidized triglyceride oil is selected from a bio-based epoxidized triglyceride or a bio-based acrylated epoxidized triglyceride. The non-aromatic cross-linking compound is selected from itaconic acid or itaconic anhydride, and the energy activated catalyst is activated by UV radiation or heat.
Type:
Grant
Filed:
June 4, 2008
Date of Patent:
October 8, 2013
Assignee:
South Dakota School of Mines and Technology