Abstract: The present invention relates to the modification of butyl elastomers, particularly halobutyl elastomers, under solvent free conditions with a phase transfer catalyst in the presence of an alkyl metal salt of an oxygen or sulfur-based nucleophile.

Abstract: Disclosed are propylene-based polymers with improved melt strength, improved strain hardening characteristics and processes for producing the same. The processes include reacting a polyamine with a maleic anhydride-grafted-propylene-based polymer. The processes produce a rheology-modified propylene-based polymer with long chain branching by forming a polyimide linkage which couples polymer chains of the propylene-based polymer. The polyimide-coupled propylene-based polymer exhibits improved melt strength and improved strain hardening characteristics.

Abstract: The present disclosure provides propylene-based polymers which exhibit a strain hardening distribution factor that is less than zero and/or a strain hardening factor greater than 1.5. The propylene-based polymers are rheology-modified by way of silane coupling to improve melt strength.

Abstract: A process for preparing a functionalised polyolefin is described. The process comprises the step of reacting: (i) a polyolefin, (ii) a compound containing a functional group, and (iii) a coagent compound having Formula I: Xn—Y—Zm??(I) wherein: Y is a core moiety; Z is a moiety containing a carbon-carbon double bond or a carbon-carbon triple bond; X is a moiety different than Z and the bond between X and Y may be a single bond or a double bond; n is a whole number greater than or equal to 0; m is a whole number greater than or equal to 2; and m+n equals a number up to the valence of Y; wherein: (a) when m is 2 and n is 0, the process comprises initially reacting the polyolefin and the coagent to form a product that is then reacted with the compound containing the functional group, and (b) the compound containing a functional group is substantially inert in free radical-mediated polymerization reactions and in free radical-mediated grafting reactions.

Abstract: Preparation of butyl rubber based graft co-polymers from halobutyl elastomers using phase transfer catalysts in the presence of a solution of an alkali metal salt of an oxygen or sulfur nucleophile that is bound to a polymeric substrate. Graft co-polymers can be produced of a butyl polymer (isobutene-co-isoprene) and polymeric substrates such as polyethylene, polypropylene, polystyrene, polybutadiene, polysilanes, polysiloxanes, polyethylene glycol, polyethylene oxide, polyphosphazenes, polyferrocenes or their hybrids.

Abstract: The present invention relates to the modification of butyl elastomers, particularly halobutyl elastomers, under solvent free conditions with a phase transfer catalyst in the presence of an alkyl metal salt of an oxygen or sulfur-based nucleophile.

Abstract: The present invention relates to a grafted liquid polymer comprising a polymer of a C4 to C7 monoolefin monomer and a C4 to C14 multiolefin monomer, a grafting material and a free radical initiator and to a process for the preparation of the grafted liquid polymer. More specifically, a liquid maleated butyl rubber composition is disclosed. The present invention also relates to grafted liquid polymer compositions which are curable in the presence of multifunctional amines. The compositions of the invention are used in a variety of applications, including injection molded fuel cells gaskets, adhesives, sealants or as polyurethane substrates.

Abstract: The present invention yields a triallyl phosphate (TAP)-mediated, rheology-modified polymer being prepared in a reaction from a reaction mixture made from or containing (a) a free-radical, chain-scissionable organic polymer and (b) TAP, wherein the TAP-mediated, rheology-modified polymer has extensional viscosity at Hencky strains above one greater than that of the free-radical, chain-scissionable organic polymer and/or a Relaxation Spectra Index (RSI) greater than that of the free-radical, chain-scissionable organic polymer.

Abstract: The present invention provides a process for preparing a filled halobutyl elastomer, which includes mixing a halobutyl elastomer with at least one mineral filler and at least one phosphine modifier and optionally curing the filled elastomer with sulfur or other curative systems. Filled halobutyl elastomers prepared according to the present invention possess improved levels of filler dispersion which results in a reduction in the hardness of the compound and an increased tensile strength.