Arlanxeo Singapore Pte. Ltd.

Lanxess International Sa

The University of Waterloo

Lanxess Corporation

Arlanxeo Deutschland Gmbh

University of Windsor

Arlanxeo Canada Inc.

Lanxss, Inc.

Gregory J E Davidson

Sharon X Guo

Dana K Adkinson

Lorenzo Ferrari

Paul Nguyen

Conrad Siegers

Mario Gauthier

Sean Malmberg

Sarah Elliott

Brianna Binder

Treena Crockett

Kuruppu Jayatissa

Gilles J Arsenault

Kevin Kulbaba

Tricia Breen Carmichael

Jessica Watson

Phil Magill

Sarah Chadder

Ralf-Ingo Schenkel

Mark William Ingratta

Richard Samuel Steevensz

Thomas Foellinger

Jacob Rawski

Kai Cao

Jessica Lee Watson

Richard Steevensz

The invention relates to an energy efficient, fast and environmentally favourable process for the preparation of chlorinated butyl rubbers, that uses hypochloric acid (HOCl) and/or dichlorine monoxide (ClO) as halogenating agent. The chlorinated butyl rubbers prepared according to the aforementioned process exhibit an advantageous microstructure and a desirable content and ratio of chlorinated and non-chlorinated oligomers and are therefore also encompassed by the invention. The teachings herein also relate to chlorinated copolymers and polymer products that include a chlorinated copolymer.

Chlorinated copolymers and polymer products including chlorinated copolymer

A process for producing a halogenated isoolefin copolymer involves contacting an unsaturated isoolefin copolymer cement, the cement comprising an unsaturated isoolefin copolymer dissolved in an organic solvent, under halogenation conditions with a halogenating agent and an aqueous solution of a potassium salt-based oxidant to form a two-phase reaction medium comprising an organic phase and an aqueous phase, the oxidant capable of converting hydrogen halide to free halogen. The process provides improved halogen recovery, is less sensitive to the presence of water, and makes use of more stable and less environmentally damaging oxidants.

Halogen recovery with K+-containing oxidant in a process for halogenating unsaturated isoolefin copolymer

The invention relates to an energy efficient, fast and environmentally favourable process for the preparation of chlorinated butyl rubbers, that uses hypochlorous acid (HOCl) and/or dichlorine monoxide (ClO) as halogenating agent. The process comprises reacting a copolymer with hypochlorous acid and/or dichlorine oxide. The copolymer comprises units derived from an isoolefin monomer and units derived from a multiolefin monomer. A preferred isoolefin is isobutene and a preferred multiolefin is isoprene.

Process for producing chlorinated butyl rubber

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.

Treatment of epoxidized unsaturated isoolefin copolymers

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.

Electronic devices comprising butyl rubber

A polyisoolefin-based polymer composition having a multimodal molecular weight distribution is described, which can be prepared by the late addition of a chain transfer agent to the polymerization process. The polymer composition has a low molecular weight fraction having a peak molecular weight (M) of less than about 100,000 g/mol and a high molecular weight fraction having a peak molecular weight (M) of greater than about 250,000 g/mol, the low molecular weight fraction present in the composition in an amount less than the high molecular weight fraction. Cured articles produced from the polyisoolefin-based polymer composition exhibit improved processability while maintaining physical properties.

Multi-modal polyisoolefin compositions and processes therefor

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.

Butyl rubber containing allylic alcohol

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 polymer 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.

Polymer compositions having a halo-containing polymer with a multi-functional phosphine linkage

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.

Process for epoxidation of unsaturated polymer

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.

Phosphonium ionomers comprising pendant vinyl groups and processes for preparing same

The present invention is directed to a process for preparing epoxidized polymers. The process comprises reacting an unsaturated polymer with hydrogen peroxide in the presence of a polymer support having a sulfonic acid group. The present invention is also directed to an epoxidized halogenated-polymer which comprises repeating units derived from at least one isoolefin monomer and repeating units derived from at least one diolefinic monomer, and one or more allylic halide groups and one or more oxirane functional groups in the polymer backbone.

Processes for preparing epoxidized polymers

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.

Ionomer comprising pendant vinyl groups and processes for preparing same

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.

Azidated copolymers and processes for preparing same

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.

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London, Canada

Gregory J E Davidson