Abstract: A process for producing a crosslinked polymer involves contacting an epoxidized unsaturated isoolefin copolymer with a catalytic amount of an acid in an absence of a solvent. A process for producing a hydroxylated unsaturated isoolefin copolymer involves contacting an epoxidized unsaturated isoolefin copolymer with a catalytic amount of an acid in an absence of a solvent. A hydroxylated unsaturated isoolefin copolymer having hydroxyl groups in endo configurations may be produced thereby.

Abstract: This invention relates to elastomeric coatings for electronics. Disclosed is a electronic device comprising a substrate layer, a conductive layer and an encapsulant layer. The encapsulant layer comprises at least a butyl rubber material. The butyl rubber encapsulant prevents a change in resistivity of the conductive layer following exposure to nitric acid vapour for 12 hours or hydrochloric acid vapour for 10 hours.

Abstract: A polymer composition is provided with a multi-modal molecular weight distribution of a halo-containing polymer. The halo-containing polymer is has multi-functional phosphine linkages at less than 10% of halo sites of the halo-containing mer that were available before multi-functional phosphine linking. A process for producing a polymer composition having a multi-modal molecular weight distribution involves dispersing a multi-functional phosphine compound in a halo-containing polymer, the halo-containing polymer comprising a total number of available halo sites, and reacting the multi-functional phosphine compound with the halo-containing polymer at an elevated temperature to produce the polymer composition in which less than 10% of the total number of available halo sites are reacted with the phosphine compound to provide multi-functional phosphine linkages in the halo-containing compound.

Abstract: A process for epoxidation of an unsaturated polymer involves mixing an unsaturated polymer and a peroxy acid in an absence of solvent to produce an epoxidized polymer. The process may require no solvent, require no catalyst, require no or little applied external heat input, require no applied cooling, require less epoxidation agent, be faster and/or result in more efficient conversion of the unsaturated polymer.

Abstract: A process for producing an allylic alcohol functionalized butyl rubber involves contacting an epoxidized butyl rubber with benzoic acid, an analogue of benzoic acid or a C1-C7 alkanoic acid. The process and a polymer compound comprising the epoxidized butyl rubber and the benzoic acid, analogue of benzoic acid or a C1-C7 alkanoic acid provide a cost effective route to a polar functionalized butyl rubber, particularly to butyl rubber comprising allylic alcohol functional groups.

Abstract: The present invention relates to ionomers comprising a reaction product of the reaction between a halogenated isoolefin copolymer and at least one phosphorus based nucleophile comprising at least one pendant vinyl group. The present invention also relates to a method of preparing and curing these ionomers.

Abstract: The present invention relates to ionomers comprising a reaction product of the reaction between a) a halogenated isoolefin copolymer and b) a nucleophile having no pendant vinyl group and a nucleophile comprising at least one pendant vinyl group. The present invention also relates to a method of preparing and curing these ionomers.

Abstract: This invention relates to elastomeric coatings for electronics. Disclosed is a electronic device comprising a substrate layer, a conductive layer and an encapsulant layer. The encapsulant layer comprises at least a butyl rubber material. The butyl rubber encapsulant prevents a change in resistivity of the conductive layer following exposure to nitric acid vapour for 12 hours or hydrochloric acid vapour for 10 hours.

Abstract: The present invention relates to functionalized copolymers of isoolefins and olefinic monomers, particularly to azidated copolymers. The present invention also relates to methods of preparing such azidated copolymers. The functionalized copolymers are used in various technology areas such as surface modification, adhesion, drug delivery, compatibilization of polymer blends or motor oil and fuel additives, and in providing clean cured products without contaminant leaching and/or side products.

Abstract: The present invention relates to curing of polymers, particularly to self curing of polymers. The present invention provides a process for curing of copolymers of isoolefins and olefinic monomers. The process includes the step of reacting the copolymer with an azidation reagent to form an azidated copolymer and then heating the azidated copolymer at a suitable temperature to cure the polymer.

Abstract: The present invention is directed to a method for preparing isobutene from a renewable source and their use in the preparation of renewable polymers. The invention also discloses purification of isobutene, selective removal of 1-butene, cis-2-butene and trans-2-butene using microporous adsorbent material, and the oligomerization of the purified liquid isobutene yielding diisobutenes and triisobutenes.

Abstract: The present invention relates to ionomers comprising a reaction product of the reaction between a halogenated isoolefin copolymer and at least one phosphorus based nucleophile comprising at least one pendant vinyl group. The present invention also relates to a method of preparing and curing these ionomers.