A novel process can be used for preparing high-reactivity isobutene homo- or copolymers, by polymerizing isobutene or an isobutene-containing monomer mixture in the presence of a polymerization catalyst.

Copolymer compositions and methods of making copolymer compositions with enhanced stability in high temperature and high salinity environments. The copolymers include hydrophobic monomers and sulfonated monomers. The sulfonated monomers can include 2-acrylamido-2-methylpropane sulfonic acid and allyl sulfonate. The sulfonated monomers increase the stability of the polymers in harsh conditions, and in high temperature, high salinity environments. The sulfonated monomers also reduce or prevent the hydrolysis of acrylamide groups, and therefore enhance the stability of the copolymer. The copolymer compositions can be made with free radical polymerization and an initiation complex.

Copolymer compositions and methods of making copolymer compositions with enhanced stability in high temperature and high salinity environments. The copolymers include hydrophobic monomers and sulfonated monomers. The sulfonated monomers can include 2-acrylamido-2-methylpropane sulfonic acid and allyl sulfonate. The sulfonated monomers increase the stability of the polymers in harsh conditions, and in high temperature, high salinity environments. The sulfonated monomers also reduce or prevent the hydrolysis of acrylamide groups, and therefore enhance the stability of the copolymer. The copolymer compositions can be made with free radical polymerization and an initiation complex.

The system provides new methods and processes for the reaction of polymeric/oligomeric substrates with reactants comprising alkyne/alkene and/or protic nucleophilic moieties to afford functionalized polymeric/oligomeric products through the utilization of homogenous and/or heterogenous gold catalysis. More specifically, the system provides routes for reaction of polymeric/oligomeric substrates comprising varying degrees of aromatic character with alkyne/alkene bearing molecules to afford a functionalized polymeric/oligomeric product. The system additionally provides pathways wherein the inverse methodology is realized, providing functionalized materials from the reaction of polymeric substrates bearing alkyne/alkene moieties with aromatic and/or protic nucleophilic reagents. Furthermore, in a tangential methodology, the system affords functionalized polymeric materials from the reaction of polymeric substrates bearing protic nucleophilic substituents with alkyne/alkene containing molecules. The system provides pathways for the facile modification of commodity polymer materials in order to produce value-added materials utilizing current polymer infrastructure, commodity polymer feedstocks, and post-consumer plastic waste.

The system provides new methods and processes for the reaction of polymeric/oligomeric substrates with reactants comprising alkyne/alkene and/or protic nucleophilic moieties to afford functionalized polymeric/oligomeric products through the utilization of homogenous and/or heterogenous gold catalysis. More specifically, the system provides routes for reaction of polymeric/oligomeric substrates comprising varying degrees of aromatic character with alkyne/alkene bearing molecules to afford a functionalized polymeric/oligomeric product. The system additionally provides pathways wherein the inverse methodology is realized, providing functionalized materials from the reaction of polymeric substrates bearing alkyne/alkene moieties with aromatic and/or protic nucleophilic reagents. Furthermore, in a tangential methodology, the system affords functionalized polymeric materials from the reaction of polymeric substrates bearing protic nucleophilic substituents with alkyne/alkene containing molecules. The system provides pathways for the facile modification of commodity polymer materials in order to produce value-added materials utilizing current polymer infrastructure, commodity polymer feedstocks, and post-consumer plastic waste.

A method can be used for manufacturing an ethylene-propylene-diene terpolymer for a fuel cell. A polymerization step includes subjecting an organic chelate compound forming a coordinate bond, a vanadium-based Ziegler-Natta catalyst, an organoaluminum compound, and ethylene, propylene, and diene monomers, together with a solvent, to polymerization in a reactor. A separation step includes recovering residual catalysts and unreacted monomers from the stream discharged from the reactor. An acquisition step includes recovering the solvent from the stream deprived of the residual catalysts and unreacted monomers to acquire the ethylene-propylene-diene terpolymer.

Acrylonitrile-Butadiene-Styrene molding compositions having improved organoleptic properties comprising a rubber modified vinylaromatic copolymer composition obtained by mass (bulk) or solution polymerization in a continuous process, and use of these molding compositions for various applications (e.g. automotive parts) are described.

Acrylonitrile-Butadiene-Styrene molding compositions having improved organoleptic properties comprising a rubber modified vinylaromatic copolymer composition obtained by mass (bulk) or solution polymerization in a continuous process, and use of these molding compositions for various applications (e.g. automotive parts) are described.

The catalyst system includes a heterogeneous procatalyst and a hydrogenation procatalyst. The heterogeneous procatalyst includes a titanium species, an aluminum species, and a magnesium chloride component. The hydrogenation procatalyst has the formula Cp.sub.2TiX.sub.2, In formula Cp.sub.2TiX.sub.2, each Cp is a cyclopentadienyl substituted with at least one R.sup.1, wherein R.sup.1 is (C.sub.1-C.sub.10)alkyl; and each X is independently a halogen atom.

The catalyst system includes a heterogeneous procatalyst and a hydrogenation procatalyst. The heterogeneous procatalyst includes a titanium species, an aluminum species, and a magnesium chloride component. The hydrogenation procatalyst has the formula Cp.sub.2TiX.sub.2, In formula Cp.sub.2TiX.sub.2, each Cp is a cyclopentadienyl substituted with at least one R.sup.1, wherein R.sup.1 is (C.sub.1-C.sub.10)alkyl; and each X is independently a halogen atom.