An illustrative embodiment of a manufactured surface component may be comprised of a textile material on a first face and an elastomer material on a second face, wherein said elastomer material is bonded to said textile material, wherein said manufactured surface component is substantially planarly configured, wherein an area of said first face and said second face is from about 0.04 square inches to about 4.0 square inches, wherein a thickness of said manufactured surface component is from about 0.3 mm to about 2.5 mm, and wherein said manufactured surface component is substantially free of any petrochemical-derived plastics, petrochemicals, and toxins.

An illustrative embodiment of a manufactured surface component may be comprised of a textile material on a first face and an elastomer material on a second face, wherein said elastomer material is bonded to said textile material, wherein said manufactured surface component is substantially planarly configured, wherein an area of said first face and said second face is from about 0.04 square inches to about 4.0 square inches, wherein a thickness of said manufactured surface component is from about 0.3 mm to about 2.5 mm, and wherein said manufactured surface component is substantially free of any petrochemical-derived plastics, petrochemicals, and toxins.

The present disclosure provides an epoxidized natural rubber composite and a preparation process thereof, and relates to the technical field of rubber materials. The epoxidized natural rubber composite provided by the present disclosure comprises the following preparation raw materials in parts by weight: 100 parts of epoxidized natural rubber, 1˜30 parts of peanut meal, 0.05˜0.8 parts of surfactants, 0.1˜4 parts of coagulant and 0.2˜12 parts of vulcanization processing aids. The present disclosure utilizes essential amino acids and non-essential amino acids contained in peanut meal to improve the aging resistance of the epoxidized natural rubber. After hot air aging, ozone aging and ultraviolet aging treatments, both the tensile strength retention rate and the elongation at break retention rate of the epoxidized natural rubber composites of the present disclosure can be kept above 83%.

Rubber compositions and articles made from such rubber compositions that are based upon a cross-linkable elastomer composition, the cross-linkable elastomer composition comprising, per 100 parts by weight of rubber (phr) between 70 phr and 100 phr of an epoxidized rubber component selected from an epoxidized polybutadiene rubber (eBR), an epoxidized styrene-butadiene rubber (eSBR), or combinations thereof, wherein the epoxidized rubber component has a Tg of between −80° C. and −110° C. and an epoxy-function content of between 1 mol % and 25 mol %. Such rubber compositions may further include between 30 phr and 150 phr of a plasticizing resin, silica and a coupling agent that is a monohydroxysilane polysulfide having a form (Formula I) wherein radicals R, identical or different, are hydrocarbon groups, radicals R′, identical or different, are divalent linking groups and x is equal to or greater than 2.

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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.

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.

A curative for epoxidized plant-based oils and epoxidized natural rubber is created from the reaction between a naturally occurring polyfunctional acid and an epoxidized plant-based oil is disclosed. The curative may be used to produce at least one of six different materials, wherein each type of material may be configured as a thermosetting elastomer that is crosslinked with β-hydroxyester linkages. The materials may be configured as a leather-like material, a foam material, a molded elastomer, a coating, an adhesive, and/or a rigid or semi-rigid material. Illustrative articles made from any combination of the six materials may be recycled using a mechano-chemical process to de-crosslink the thermosetting elastomer.

A curative for epoxidized plant-based oils and epoxidized natural rubber is created from the reaction between a naturally occurring polyfunctional acid and an epoxidized plant-based oil is disclosed. The curative may be used to produce at least one of six different materials, wherein each type of material may be configured as a thermosetting elastomer that is crosslinked with β-hydroxyester linkages. The materials may be configured as a leather-like material, a foam material, a molded elastomer, a coating, an adhesive, and/or a rigid or semi-rigid material. Illustrative articles made from any combination of the six materials may be recycled using a mechano-chemical process to de-crosslink the thermosetting elastomer.

Disclosed herein are highly active dilithio initiators prepared from high molecular weight dienes (C≧6) and methods for the preparation of such compounds. These dilithio initiators result in greater control over polymer microstructure and provide useful polymers and oligomers with low vinyl incorporation.

A modified diene polymer is obtained by decomposing a diene polymer having a carbon-carbon double bond in a main chain by oxidative cleavage of the carbon-carbon double bond to reduce a molecular weight, changing acido-basic properties of a system containing polymer fragments obtained such that the system is changed into a basic system when the system is acidic and the system is changed into an acidic system when the system is basic to combine the polymer fragments, thereby obtaining an intermediate polymer having an altered structure, and epoxidizing a carbon-carbon double bond moiety of a main chain of the intermediate polymer.