Abstract:
A heterogeneous in-situ polymer blend comprising a continuous phase comprising a polypropylene having a crystallinity of at least 30% and a melting point temperature Tm greater than 130° C., and a heat of fusion ΔHf greater than 65 J/g; and a dispersed phase comprising particles of an elastomeric copolymer dispersed in the continuous phase and having an average particle size of less than 5 micron, the elastomeric copolymer comprising ethylene units and 0.001 to 5 wt % diene by weight of the copolymer, and having a crystallinity of less than 20% and being at least partially cross-linked such that the degree of cross-link is at least 20%.
Abstract:
Provided herein is a process for making a grafted cross-linked polymer blend, by polymerizing a first and second polymer solution (each having 75 to 99 wt % propylene-derived units, 1 to 25 wt % ethylene-derived units, and 0.05 to 6 wt % diene-derived units); combining the first and second polymer solution to produce a polymer blend solution; removing solvent from the polymer blend solution to produce a polymer blend; mixing the polymer blend with a coagent and a vinyl-terminated silane compound; subjecting the polymer blend to electron beam irradiation to grafting the vinyl-terminated silane compound to either or both of the first polymer and the second polymer to form a grafted polymer blend; and moisture curing the grafted polymer blend to form a grafted cross-linked polymer blend, wherein the grafted cross-linked polymer blend is substantially free of peroxide.
Abstract:
A heterogeneous vulcanized polymer blend comprising a continuous phase comprising a thermoplastic polypropylene having a crystallinity of at least 30% and a dispersed phase comprising particles of an elastomeric copolymer dispersed in the continuous phase and having an average particle size of less than 5 micron. The elastomeric copolymer has a crystallinity of less than 20% and is at least partially cross-linked such that no more than about 80 wt % of the elastomeric copolymer is extractable in cyclohexane at 23° C.
Abstract:
Rubber compounds that comprise rubber and propylene-a-olefin-diene (PE(D)M) polymers may be useful in tire-related articles (e.g., tire sidewalls, inner tubes, and innerliners). Such a rubber compound may comprise: about 5 phr to about 50 phr of the PE(D)M polymer that comprises about 65 wt % to about 99.5 wt % propylene, about 0.5 wt % to about 35 wt % a-olefin that is not propylene, and 0 wt % to about 20 wt % diene, said wt % based on the weight of the PE(D)M polymer, and about 50 parts per hundred parts rubber (phr) to about 95 phr of a rubber that comprises one selected from the group consisting of the halogenated isobutylene-based rubber is selected from the group consisting of: natural rubber, polyisoprene rubber, poly(styrene-co-butadiene) rubber, polybutadiene rubber, poly(isoprene-co-butadiene) rubber, styrene-isoprene-butadiene rubber, butyl rubber, star branched butyl rubber, isobutylene-isoprene rubber, poly(isobutylene-co-alkylstyrene), a halogenated isobutylene-based rubber, polychloroprene rubber, nitrile rubber, and any combination thereof.
Abstract:
A tire tread composition is disclosed. The tire tread composition includes components, by weight of the composition, within the range from: 5 to 75 wt % of a diene elastomer; 0 to 40 wt % of processing oil; 20 to 80 wt % of filler; a curative agent; and 5 to 30 wt % of a propylene-ethylene-diene terpolymer containing from 2 wt % to 40 wt % of ethylene and/or C4-C20 α-olefins derived units, from 0.5 to 10 wt % of diene derived units, and having a heat of fusion, as determined by DSC, of from 0 J/g to 80 J/g.
Abstract:
A tire tread composition is disclosed. The tire tread composition includes components, by weight of the composition, within the range from: 5 to 75 wt % of a diene elastomer; 0 to 40 wt % of processing oil; 20 to 80 wt % of filler; a curative agent; and 5 to 30 wt % of a propylene-ethylene-diene terpolymer containing from 2 wt % to 40 wt % of ethylene and/or C4-C20 α-olefins derived units, from 0.5 to 10 wt % of diene derived units, and having a heat of fusion, as determined by DSC, of from 0 J/g to 80 J/g.
Abstract:
The present invention is related to an article comprising a substrate, having at least one propylene terpolymer comprising propylene derived units, one or more dienes, and an alpha-olefin content of less than about 35 wt % of the propylene terpolymer; and an adhesive composition, having about 20 to about 80 wt % of a polymer blend comprising a first propylene-based polymer, that is a homopolymer of propylene or a copolymer of propylene and ethylene or a C4 to C10 alpha-olefin, and a second propylene-based polymer, that is a homopolymer of propylene or a copolymer of propylene and ethylene or a C4 to C10 alpha-olefin; wherein the second propylene-based polymer is different than the first propylene-based polymer; and wherein the adhesive composition is applied to the substrate at temperature of less than about 150° C.
Abstract:
A heterogeneous vulcanized polymer blend comprising a continuous phase comprising a thermoplastic polypropylene having a crystallinity of at least 30% and a dispersed phase comprising particles of an elastomeric copolymer dispersed in the continuous phase and having an average particle size of less than 5 micron. The elastomeric copolymer has a crystallinity of less than 20% and is at least partially cross-linked such that no more than about 80 wt % of the elastomeric copolymer is extractable in cyclohexane at 23° C.
Abstract:
Provided herein is a process for making a grafted cross-linked polymer blend, by polymerizing a first and second polymer solution (each having 75 to 99 wt % propylene-derived units, 1 to 25 wt % ethylene-derived units, and 0.05 to 6 wt % diene-derived units); combining the first and second polymer solution to produce a polymer blend solution; removing solvent from the polymer blend solution to produce a polymer blend; mixing the polymer blend with a coagent and a vinyl-terminated silane compound; subjecting the polymer blend to electron beam irradiation to grafting the vinyl-terminated silane compound to either or both of the first polymer and the second polymer to form a grafted polymer blend; and moisture curing the grafted polymer blend to form a grafted cross-linked polymer blend, wherein the grafted cross-linked polymer blend is substantially free of peroxide.
Abstract:
A heterogeneous in-situ polymer blend comprising a continuous phase comprising a polypropylene having a crystallinity of at least 30% and a melting point temperature Tm greater than 130° C., and a heat of fusion ΔHf greater than 65 J/g; and a dispersed phase comprising particles of an elastomeric copolymer dispersed in the continuous phase and having an average particle size of less than 5 micron, the elastomeric copolymer comprising ethylene units and 0.001 to 5 wt % diene by weight of the copolymer, and having a crystallinity of less than 20% and being at least partially cross-linked such that the degree of cross-link is at least 20%.