Abstract: An improved thermoset polymer having good mechanical properties and no detectable dicyclopentadiene odor is obtained by the ring-opening polymerization of a novel mixture of adducts comprising divinyl cyclohydrocarbon compound, such as 3,5-divinylcyclopentene and cyclopentadiene, optionally with added cycloolefinic compound, such as dicyclopentadiene, at polymerization conditions in the presence of an olefin metathesis catalyst.

Abstract: A catalyst and process for the polymerization of cyclic olefins, such as dicyclopentadiene, are disclosed. The catalyst comprises the reaction product of a transition metal halide and a biphenol. Polymerization can be carried out in a reaction injection molding process to prepare a thermoset molded article.

Abstract: A hard, infusible, crosslinked polymeric product free from detectable cyclopentadiene odor is obtained by contacting, under polymerization conditions, a mixture of Diels-Alder adducts of 4-vinylcyclohexene and cyclopentadiene and Diels-Alder oligomers of cyclopentadiene of at least 3 cyclopentadiene units with an olefin methathesis catalyst.

Abstract: Described herein are novel monomers, polyketals derived from such monomer, improved process for the production of such monomers and a process for producing the polyketals.

Abstract: A catalyst and process for the polymerization of cyclic olefins, such as dicyclopentadiene, are disclosed. The catalyst includes a transition metal compound and a borohydride co-catalyst, with optional boron halide promoter. Polymerization can be carried out in a reaction injection molding process to prepare a thermoset molded article.

Abstract: Described herein are novel monomers, polyketals derived from such monomer, improved process for the production of such monomers and a process for producing the polyketals.

Abstract: Described herein are crystalline block polymers and chain extended polymers containing blocks of crystalline poly(aryl ether ketones). Also, described herein are monomers and oligomers suitable for preparing the crystalline block polymers and chain-extended polymers. Further, described herein are methods for producing the crystalline block and chain-extended polymers, as well as the monomers and oligomers.

Abstract: Described herein is process for preparing polyaryletherketones from a polyketal by converting the polyketal to a polyaryletherketone in the presence of a Group IIA, IIB, IVA, VIIB, IIIA, IVB, IB or VIII metal salt.

Abstract: Described herein is a method for preventing molecular weight degradation in the preparation of poly(aryl ether sulfones) by nucleophilic displacement polycondensation reactions. This method comprises the addition of an effective amount of a sodium, lithium, alkaline earth or lanthanide metal salt to the polycondensation reaction to control the molecular weight of the poly(aryl ether sulfone).

Abstract: Described herein are novel substantially linear monomeric compositions which can be polymerized with one or more difunctional monomers to give novel polymeric compositions having liquid crystal properties. This invention is also directed to a process for preparation of the novel substantially linear monomeric compositions.

Abstract: Described herein are poly(aryl ether ketones) derived from biphenol which can be improved by incorporating bisphenol comonomers. The resulting polymers have lower melting points while the Tg is essentially unchanged resulting in good mechanical and crystallization properties.

Abstract: The method of preparing a thermoplastic polyarylether polymer which comprises reacting a first monomer composition comprising an activated dihalobenzenoid compound and a dihydroxydiphenyl aliphatic monomer in a molar ratio of dihalobenzenoid compound to dihydroxybenzenoid compound of at least 1.2 to 1, adding to the product a second monomer composition comprising a dihydroxybenzenoid compound comprising at least one compound which is free of aliphatic moieties and polymerizing.

Abstract: The method of preparing a thermoplastic polyarylether polymer which comprises reacting a first monomer composition comprising an activated dihalobenzenoid compound and dihydroxybenzenoid composition comprising hydroquinone, adding to the product a second monomer composition comprising a dihydroxybenzenoid composition consisting essentially of Bis-(hydroxyphenyl) compounds in a concentration of at least 50 mole percent of the total Bis-(hydroxyphenyl) compounds added in the monomer compositions and polymerizing.

Abstract: Described herein are crystalline block polymers and chain extended polymers containing blocks of crystalline poly(aryl ether ketones). Also, described herein are monomers and oligomers suitable for preparing the crystalline block polymers and chain-extended polymers. Further, described herein are methods for producing the crystalline block and chain-extended polymers, as well as the monomers and oligomers.

Abstract: Described herein are novel monomers, polyketals derived from such monomer, improved process for the production of such monomers and a process for producing the polyketals.

Abstract: Described herein is an improved process for preparing poly(aryl ethers) and poly(aryl ether ketones) by the reaction of a mixture of at least one bisphenol and at least one dihalobenzenoid compound, and/or a halophenol, in which the improvement comprises providing to the reaction medium, a combination of sodium or an alkaline earth metal carbonate and/or bicarbonate and a potassium, rubidium, or cesium salt of an organic acid or combinations of various organic salts thereof. The process yields high molecular weight, linear, poly(aryl ethers) and poly(aryl ether ketones) possessing excellent thermal stability and physical properties.

Abstract: Described herein is an improved process for preparing poly(aryl ether ketones) by a nucleophilic displacement polycondensation reaction wherein the improvement comprises adding an alkali, alkaline earth, or lanthanide metal salt to the polycondensation reaction.

Abstract: Described herein are poly(aryl ether ketones) derived from biphenol which can be improved by incorporating bisphenol comonomers. The resulting polymers have lower melting points while the Tg is essentially unchanged resulting in good mechanical and crystallization properties.

Abstract: Described herein is an improved process for preparing poly(aryl ether ketone)s by reacting a mixture of at least one bisphenol and at least one dihalobenzenoid compound or halophenol, wherein the improvement comprises providing to the reaction, a combination of sodium carbonate and/or bicarbonate and an alkali metal halide selected from potassium, rubidium or cesium fluoride or chloride, or combinations thereof.

Abstract: Poly(aryl ether) resins having repeat units of the structure--O--E--O--E'--wherein E is the residuum of a dihydric phenol and E' is the residuum of a benzenoid compound having an inert electron withdrawing group in at least one of the positions ortho and para to the valence bonds, can be sulfonated by first reacting with a silyl halosulfonate, or the combination of a silyl halide and a halosulfonic acid, to form a resin having pendant silyl sulfonate groups, followed by the base cleavage of the silyl moiety to form the sulfonated resin. The sulfonated resins may be used to make membranes.