Patent classifications
C08G65/4087
Method for the manufacture of poly(aryl ethers) using at least one organic base
The present invention relates to a method for the manufacture of a poly(aryl ether) such as a poly(aryl ethersulfone) or a poly(aryl ether ketone) including the use of an organic base having a pKa of at least 10.
POLY(ARYLENE ETHER KETONE) RESIN, METHOD FOR PRODUCING THE SAME, AND MOLDED ARTICLE
Provided is a poly(arylene ether ketone) resin which inhibits reactions such as molecular weight extension and crosslinking in a high-temperature molten state and which is excellent in melt viscosity stability and molding processability. The poly(arylene ether ketone) resin contains an alkylsulfonyl group represented by general formula (1). In the formula, R is an alkyl group containing one to four carbon atoms.
PROCESS FOR THE PREPARATION OF EUGENOL POLYETHERS THAT CAN BE HYDROSILYLATED AND EUGENOL POLYETHERSILOXANES AND USE THEREOF
The present invention relates to a process for producing hydrosilylatable, eugenol-based polyethers, to the conversion thereof into polyether siloxanes and also to the products that may be produced by this process and to the use of said products as surfactants.
High purity diphenyl sulfone, preparation and use thereof for the preparation of a poly(aryletherketone)
The presence of certain impurities in diphenyl sulfone have a deleterious effect on the properties of the poly(aryletherketone)s produced therein, including one or more of color, melt stability, molecular weight, crystallinity, etc. and here identify those impurities and provide processes for the recovery of the diphenyl sulfone.
FUNCTIONALIZED POLY(ARYL ETHER SULFONES) COPOLYMERS
The invention relates to a side-chain functionalized copolymer (P1) and to the process for preparing the side-chain functionalized copolymer (P1). The present invention also relates to the use of the copolymer (P1) in the preparation of a membrane, a composite material or a coating.
METHOD FOR PRODUCING AROMATIC POLYETHER, AND POTASSIUM CARBONATE USED IN SAME
Provided is a method for producing an aromatic polyether, comprising reacting 4,4′-dichlorobenzophenone and hydroquinone in the presence of a potassium carbonate satisfying at least one of the following conditions (A) and (B): (A) the potassium carbonate has a bulk density of 1.2 g/ml or less; and (B) an average particle diameter D (.Math.m) and a specific surface area S (m.sup.2/g) of the potassium carbonate satisfy D/S≤600.
POLY(ARYL ETHER) BASED POLYMERS AND ASSOCIATED GAS SEPARATION MEMBRANES
Compositions and methods related to the synthesis and application of poly(aryl ether)s are generally described.
METHOD FOR CONTINUOUSLY PRODUCING AROMATIC POLYETHER
A method for continuously producing an aromatic polyether according to the present invention includes simultaneously implementing: a supply step of supplying a polymerization solvent, an alkali metal compound, and a raw material; a polymerizing step; and a movement step. The alkali metal compound is supplied as an aqueous mixture. According to the present invention, clogging of piping in the continuous production apparatus can be suppressed, and the aromatic polyether can be stably obtained.
Poly(phenylene ether) copolymer process and compositions
A poly(phenylene ether) copolymer of 2-methyl-6-phenylphenol and a dihydric phenol having an absolute number average molecular weight of 1,000 to 10,000 grams/mole is made by polymerization of 2-methyl-6-phenylphenol and a dihydric phenol in the presence of molecular oxygen, a polymerization catalyst comprising a metal ion and at least one amine ligand, and a solvent composed of at least 95 weight percent of a C.sub.1-C.sub.3 alcohol selected from methanol, ethanol, 1-propanol, and 2-propanol. The poly(phenylene ether) copolymer can be, for example, a copolymer of 2-methyl-6-phenylphenol, 2,2-bis(3,5-dimethyl-4-hydroxyphenol)propane, and optionally 2,6-dimethylphenol. The poly(phenylene ether) copolymer finds utility in curable compositions, cured compositions, and articles.
Polyether-epoxide polymer compositions
Polyether-epoxide polymer compositions are disclosed. The compositions comprise a reaction product of a polyepoxide compound and a polyol composition comprising a polyether polyol. The ratio of epoxy equivalents to hydroxyl equivalents is within the range of 0.5:1 to 3:1. The polyether-epoxide composition has a T.sub.g within the range of −40° C. to 60° C. The polyether polyol has a hydroxyl value within the range of 150 to 800 mg KOH/g and an average hydroxyl functionality within the range of 3.5 to 8.0. In some aspects, the polyol composition further comprises a polyester polyol. Low- and elevated-temperature processes catalyzed by bases or Lewis acids for making the polyether-epoxide compositions are also disclosed. In a simple yet innovative approach, a new class of polymers useful for coatings, elastomers, adhesives, sealants, and other valuable products is assembled from readily available starting materials without reliance on polyamines or polyisocyanates.