Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 30 to about 50 phr of polybutadiene having a cis-1,4 linkage content of at least 95%; about 40 to about 70 phr of styrene/butadiene copolymer; about 0 to about 20 phr of natural rubber or polyisoprene; about 0 to about 30 phr of a processing oil; about 10 to about 30 phr of a hydrocarbon resin; about 50 to about 75 phr of a filler; a curative agent; an antioxidant; a silane coupling agent; and about 5 to about 30 phr of a butyl copolymer rubber containing about 85 to about 99.5 mol % C4-C7 isoolefin(s) and from about 0.5 to about 15 mol % C4-C14 conjugated dienes.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 30 to about 70 phr of polybutadiene having a cis- 1,4 linkage content of at least 95%; about 30 to 70 phr of natural rubber or polyisoprene; about 20 to 50 phr of a processing oil; a curative agent; an antioxidant; about 50 to about 80 phr filler; a silane compling agent; and about 5 to about 30 phr of a polymer selected from the group consisting of ethylene-propylene-diene terpolymer, butyl mbber, poly(isobutylene-co- para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer. The polymer based on ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer may be functionalized.

Abstract: A supported catalyst system is based on a transition metal carbene including the moiety M1=CR*)2, wherein M1 is the transition metal and R* is hydrogen or a C1-C8 hydrocarbyl. The catalyst system can be supported on a metal oxide support such as silica or the catalyst can be self-supporting. Methods of making the catalyst system can involve precursors based on and/or reacted with aluminum alkyls, halides, and/or alkoxides. Methods of polymerizing cyclic olefins with the catalyst system can obtain polyalkenamers, cyclic olefin polymers, cyclic olefin copolymers, and other metathesis reaction products. The supported catalyst and/or monomer can be recovered and recycled to the polymerization reactor.

Abstract: Methods of post-polymerization modification of a polymer are provided herein. The present methods comprise the step of reacting a polymer with at least one nucleophile in a nucleophilic substitution reaction performed without a solvent to produce a functionalized polymer. The nucleophile can be selected from the group consisting of thioacetate, phenoxide, alkoxide, carboxylate, thiolate, thiocarboxylate, dithiocarboxylate, thiourea, thiocarbamate, dithiocarbamate, xanthate, thiocyanate. Nucleophilic substitution reaction can be performed in the presence of a phase transfer catalyst. Nucleophilic substitution reaction can also be performed via a two-step in-situ reactive mixing process with the initial formation of the polymer-amine ionomer (polymer-NR3+Br) which catalyzes the subsequent nucleophilic substitution with a second nucleophile to form a bi-functional polymer.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 5 to about 40 phr of styrene/butadiene copolymer; about 60 to about 100 phr of natural mbber or polyisoprene; a curative agent; an antioxidant; about 1 to about 20 phr carbon black; about 5 to about 40 phr plasticizing agent; about 40 to about 80 phr silica; about 1 to about 20 phr silane coupling agent and about 5 to about 30 phr of a polymer selected from the group consisting of ethyl-ene-propylene-diene terpolymer, butyl mbber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer. The polymer based on ethylene-propylene-diene terpolymer, butyl mbber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer may be functionalized.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): 0 to about 50 phr of a polybutadiene having a cis-1,4 linkage content of at least 95%; about 50 to 100 phr of natural rubber or polyisoprene; a curative agent; an antioxidant; about 10 to about 80 phr carbon black; optionally about 30 to about 70 phr silica; about 1 to about 20 phr hydrocarbon resin; and about 5 to about 30 phr of a polymer selected from the group consisting of ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methyl-styrene-co-isoprene) terpolymer. The polymer based on ethylene-propylene-diene terpolymer, butyl rubber, oly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer may be functionalized.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 5 to about 30 phr of polybutadiene having a cis-1,4 linkage content of at least 95%; about 60 to 100 phr of a styrene/butadiene copolymer; an antioxidant; a curative agent; about 1 to about 20 phr carbon black; about 50 to 80 phr silica, a silane coupling agent and about 5 to about 30 phr of a polymer is selected from the group consisting of ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer. The polymer based on ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer may be functionalized.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 60 to about 100 phr of polybutadiene having a cis-1,4 linkage content of at least 95%; about 5 to 40 phr of a styrene/butadiene copolymer; a curative agent; an antioxidant; about 50 to about 80 phr hydrocarbon resin; about 100 to about 140 phr silica; about 1 to about 20 phr silane coupling agent and about 5 to about 30 phr of a polymer selected from the group consisting of ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methyl-styrene-co-isoprene) terpolymer. The polymer based on ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer may be functionalized.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 5 to about 30 phr of polybutadiene having a cis-1,4 linkage content of at least 95%; about 60 to 100 phr of a styrene/butadiene copolymer; an antioxidant; about 1 to about 20 phr carbon black; about 100-140 phr silica; a silane coupling agent and about 5 to about 40 phr of a polymer selected from the group consisting of ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly (isobutylene-co-para-methylstyrene-co-isoprene) terpolymer. The polymer based on ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly (isobutylene-co-para-methylstyrene-co-isoprene) terpolymer may be functionalized.

Abstract: An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 20 to about 40 phr of a polybutadiene having a cis-1,4 linkage content of at least 95%; about 40 to about 70 phr styrene/ butadiene copolymer; about 5 to about 30 phr natural rubber or polyisoprene; a curative agent; an antioxidant; about 1 to about 20 phr carbon black; about 1 to about 30 phr plasticizing oil; about 40 to about 80 phr silica; about 1 to about 15 phr silane coupling agent and about 5 to about 30 phr of a polymer selected from the group consisting of an ethylene-propylene-diene terpolymer, butyl rubber, poly(isobutylene-co-para-methylstyrene) and poly(isobutylene-co-para-methylstyrene-co-isoprene) terpolymer.

Abstract: This invention relates to sulfur, vulcanization accelerator and carbon black master batch formulations comprising either a semi-crystalline propylene-olefin copolymer or a combination of a semi-crystalline propylene-olefin copolymer and a hydrocarbon resin. The semi-crystalline propylene-olefin copolymer or the combination of semi-crystalline propylene-olefin copolymer and hydrocarbon resin imparts a high hardness property to the carbon black, sulfur and accelerator master batch formulations thereby preventing pellet agglomeration during storage and allowing for ease in material handling.

Abstract: Thermoplastic vulcanizate compositions and articles exhibiting superior elastomeric performance and adhesive properties, and methods of making same are characterized by comprising a thermoplastic phase and a rubber phase. The thermoplastic phase comprises a thermoplastic polyolefin, and the rubber phase comprises an amorphous propylene-ethylene copolymer having: a Mn of from 20 kg/mol to 3,000 kg/mol, a Mw/Mn of 10.0 or lower, an ethylene percentage by weight of from about 2 wt. % to about 50 wt. %, a diene percentage by weight of from about 0 wt. % to about 21 wt. % and a heat of fusion of less than 5 J/g.

Abstract: This invention relates to a silane-functionalized resin composition having a polymer backbone, wherein the polymer backbone is selected from at least one of C5 homopolymers and copolymer resins, terpene homopolymer or copolymer resins, pinene homopolymer or copolymer resins, C9 homopolymers and copolymer resins, C5/C9 copolymer resins, alpha-methylstyrene homopolymer or copolymer resins, and combinations thereof, and wherein the polymer backbone is substantially free of styrene copolymer; and a silane, where the ratio of the mole percent of the silane to the mole percent of the polymer backbone in the composition is in the amount of 0.04 to 3.0 as determined by H-NMR.

Abstract: A functionalized polyolefin and a tire tread composition comprising the functionalized polyolefin is described. The functionalized polyolefin comprises a vinyl/vinylidene-terminated polyolefin in which the vinyl/vinylidene terminus is functionalized with an alkoxysilane or an alkylsilane and optionally having ether, hydroxyl and/or amine functionality. The invention is also directed to the synthesis of vinyl/vinylidene-terminated polyolefins, functionalization at the vinyl/vinylidene terminus with an alkoxysilane or an alkylsilane and optionally having ether, hydroxyl and/or amine functionality.

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 ?-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: Elastomeric compositions comprising propylene-ethylene-diene terpolymer based polyolefin additives useful in tire tread compositions. The elastomeric compositions comprise 100 phr (parts by weight per hundred parts of total elastomer) diene elastomers; about 0 to about 80 phr of processing oil; 0 to about 80 phr of a hydrocarbon resin; about 60 to about 140 phr of filler; a curative agent; and about 5 to about 30 phr of a silane functionalized propylene-ethylene-diene terpolymer. The silane functionalized propylene-ethylene-diene terpolymer comprises from about 2 wt. % to about 40 wt. % of ethylene and/or C4-C20 ?-olefins derived units, from 0.5 to 10 wt % of diene derived units, and a silane coupling agent. The present elastomeric compositions are useful as tire tread compositions for improved tire performance.

Abstract: This invention relates to production of propylene-predominant copolymers using a transition metal complex and at least two different non-coordinating anion activators. An olefinic feed comprising a C3-C40 alpha olefin, ethylene, and a diene monomer is contacted under polymerization reaction conditions with a catalyst system comprising a first non-coordinating anion activator, a second non-coordinating borate activator differing from the first non-coordinating anion activator, and a transition metal complex comprising a tetrahydro-s-indacenyl or tetrahydro-as-indacenyl group bound to a group 3-6 transition metal. A molar ratio of the first non-coordinating anion activator to the second non-coordinating anion activator is sufficient to produce a melt flow rate under the polymerization reaction conditions for the resulting copolymer of about 30 g/10 min or below as determined by ASTM D-1238 (230° C., 2.16 kg).

Abstract: An elastomeric composition and method incorporating a hydrocarbon polymer modifier with improved permanence. The composition comprises elastomer, filler and silane-functionalized hydrocarbon polymer modifier (Si-HPM) made in a pre-reaction adapted to couple the Si-HPM to the elastomer, filler or both, wherein the Si-HPM comprises an interpolymer of monomers chosen from piperylenes, cyclic pentadienes, aromatics, limonenes, pinenes, amylenes, and combinations thereof.

Abstract: Systems and methods are provided for producing upgraded raffinate and extract products from lubricant boiling range feeds and/or other feeds having a boiling range of 400° F. (204° C.) to 1500° F. (816° C.) or more. The upgraded raffinate and/or extract products can have a reduced or minimized concentration of sulfur, nitrogen, metals, or a combination thereof. The reduced or minimized concentration of sulfur, nitrogen, and/or metals can be achieved by hydrotreating a suitable feed under hydrotreatment conditions corresponding to relatively low levels of feed conversion. Optionally, the feed can also dewaxed, such as by catalytic dewaxing or by solvent dewaxing. Because excessive aromatic saturation is not desired, the pressure for hydrotreatment (and optional dewaxing) can be 500 psig (˜3.4 MPa) to 1200 psig (˜8.2 MPa).

Abstract: Provided herein are thioacetate isobutylene-based polymer compositions comprising thioalkylated functionalized polymer, and a sulfur donor and/or accelerator cure system. The thioalkylated functionalized polymer is produced via nucleophilic substitution reaction in solution. The present thioacetate functionalized isobutylene-based polymer compositions together with various accelerators and sulfur donors can form thermosets useful for pharmaceutical and tire applications without the use of zinc or a zinc oxide activator.