Abstract: A process for the preparation of oligomeric poly alpha-olefins comprises oligomerizing low molecular weight PAO in the presence of an ionic liquid catalyst under oligomerization conditions. The low molecular weight PAOs used as a feed or feed component of the present process are the light olefinic by-product fraction including the dimers and light fractions from the metallocene-catalyzed PAO oligomerization process.

Abstract: A process for making a poly(alkyl epoxide). The process has the step of polymerizing one or more alkyl epoxide monomers in the presence of a cationic catalyst according to the following sequences: wherein R1, R2, R3, and R4 are hydrogen or alkyl moieties that, taken together, have a total of 1 to 80 carbons; wherein any of R1, R2, R3, and R4 can be linear or branched if it is an alkyl moiety; wherein “m” is an integer from 1 to 4; and wherein “n” is an integer from 2 to 120. There is also another process for making a poly(alkyl epoxide) using an initiator. There are also poly(alkyl epoxides). There is also a lubricant composition having a first lubricant base stock of one or more poly(alkyl epoxides) and a second lubricant base stock different than the first lubricant base stock.

Abstract: Provided is a block copolymer having an “A” block of a functionalized hydrocarbon moiety including one or more functional end groups selected from the group consisting of: epoxides, amines, acids, acid chlorides, acid anhydrides, halogens, vinyl or vinylidene double bond, aromatic rings and thiols, and a “B” block of a functionalized polyether moiety including one or more functional end groups selected from the group consisting: epoxides, amines, acids, acid chlorides, acid anhydrides, halogens, vinyl or vinylidene double bond, aromatic rings and thiols. The end group of the polyether moiety is different than the end group of the hydrocarbon moiety, and the hydrocarbon moiety and the polyether moiety are copolymerizable therewith. Preferably, the hydrocarbon moiety is a poly-?-olefin and the polyether moiety is a polyalkylene glycol.

Abstract: A lubricant base stock is provided. The base stock is a polyether of a plurality of epoxidized olefin monomeric units. The polyether has 30 carbon atoms or more. There is also a process for making a polyether.

Abstract: A poly(alpha-olefin/alkylene glycol) copolymer of the following formula: wherein R3, R4, Ra, and Rb are, independently, any of H, a C1 to C18 normal or branched alkyl radical, or a C1 to C18 aromatic radical or aromatic-containing alkyl radicals; wherein n and m, are, independently, integers from 1 to 1000; and wherein x is an integer from 0 to 10. There is also a process for making the copolymer. There is also a lubricant formulation having the copolymer.

Abstract: A modified inorganic substrate having a plurality of grafts of a polyalkyl acrylate or methacrylate of mean alkyl pendant chain length of 6 to about 40 carbons extending therefrom. The modified inorganic substrate is preferably a modified silica substrate and more preferably modified silica nanoparticles. There is also a process for graft polymerizing a silica substrate.

Abstract: A lubricant composition comprising a Group I-IV or Group VI lube base stock and a glycerol tri-ester of the formula: wherein R1, R2 and R3 are independently selected from linear or branched C4 to C14 alkyl groups.

Abstract: Disclosed are processes for preparing an epoxidized and/or hydroxylated ?-olefin/diene copolymer materials such as ethylene/dicyclopentadiene. These processes comprise contacting in a reaction medium a) a copolymeric precursor component with b) a hydrogen peroxide oxidizing agent, in the presence of alkyl-trioxorhenium-based catalyst, under certain reaction conditions. The copolymeric precursor component comprises copolymers of ?-olefins and dienes with these copolymers containing at least one double bond in each diene-derived comonomer. The reaction medium is maintained under reaction conditions which promote formation of oxirane rings at, and/or diol formation across, the sites of the diene-derived co-monomer double bonds in the copolymeric precursor material. Epoxidation and hydroxylation generally increases the glass transition temperature, Tg, of these copolymers and imbues polarity which imparts oil resistance.

Abstract: Provided is a lubricant having a first base stock of one or more alkyl cyclohexyl 1,2-dicarboxylate esters at 1 wt % to 50 wt % based on the total weight of the blend, and a second base stock at 99 wt % to 50 wt % based on the total weight of the blend, wherein the second base stock is chosen from (a) one or more C6 to C16 poly-?-olefins, (b) one or more gas-to-liquid materials, and (c) one or more Group I, II, and III oils. Also provided are methods of making such lubricant blends.

Abstract: A polymer composition comprises (a) least 40 wt % (based upon the weight of the composition) of a cyclic olefin polymer comprising at least one acyclic olefin and at least 20 wt % of one or more cyclic olefins (based upon the weight of the cyclic olefin polymer), wherein at least a portion of the cyclic olefin polymer has a glass transition temperature of greater than 100° C.; (b) an acyclic olefin polymer modifier in an amount up to 40 wt % (based upon the weight of the composition); and (c) at least 10 wt % (based upon the weight of the composition) of one of more fillers. The polymer composition has a notched Izod impact resistance measured at 23° C. of greater than 100 J/m and a flexural modulus (1% secant method) of greater than 1400 MPa.

Abstract: A process for preparing an epoxidized ?-olefin/diene copolymer including the steps of contacting in a reaction medium a) copolymers of an ?-olefin and a diene, which copolymers contain at least one double bond in each diene-derived co-monomer, with b) a hydrogen peroxide epoxidizing agent, in the presence of a perfluorinated alcohol reaction solvent, and in the absence of any metal-containing epoxidation catalyst, under reaction conditions which promote formation of oxirane rings at the sites of the diene-derived co-monomer double bonds in the copolymeric precursor material.

Abstract: This invention relates to a hydroxyaromatic functionalized polyalpha-olefin comprising the product of the combination of: a) a polyalpha-olefin comprising one or more C3 to C20 linear alpha-olefins and having at least 10% vinylidene unsaturation, a viscosity index of 80 to 400, an Mn of 300 to about 20,000, and a pour point of 0° C. or less; and b) a hydroxyaromatic moiety; wherein the analine point of the functionalized polyalpha-olefin is at least 10° C. lower than the analine point of the polyalpha-olefin.

Abstract: A process for the preparation of oligomeric poly alpha-olefins includes oligomerizing low molecular weight PAO oligomer in the presence of a Lewis acid catalyst such as promoted aluminum trichloride or boron trifluoride under oligomerization conditions. The low molecular weight PAO oligomers used as a feed or feed component of the present process are the light olefinic by-product fractions including the dimers and light fractions from the metallocene-catalyzed PAO oligomerization process which are characterized by a molecular weight of 150 to 600 and a terminal olefin (vinylidene) content of at least 25%.

Abstract: A process for the preparation of oligomeric poly alpha-olefins comprises oligomerizing low molecular weight PAO in the presence of an ionic liquid catalyst under oligomerization conditions. The low molecular weight PAOs used as a feed or feed component of the present process are the light olefinic by-product fraction including the dimers and light fractions from the metallocene-catalyzed PAO oligomerization process.

Abstract: A process is described for functionalizing a copolymer comprising units derived from at least one ?-olefin and units derived from at least one diene, which copolymer contains at least one double bond. The process comprises reacting the copolymer with at least one functionalizing agent to introduce polar pendant oxygen-containing functional groups onto the copolymer.

Abstract: Disclosed is the preparation of compositions which are mixtures of certain types of epoxidized rigid copolymers of ?-olefins and diene-derived co-monomers in combination with elastomeric diene-based polymers or copolymers. These two types of rigid and elastomeric polymeric materials are placed in a common liquid reaction medium and contacted therein with an oxidizing agent. The oxidizing agent, which can be a peroxide or peracid, epoxidizes in-situ at least a portion of the residual double bonds of the rigid copolymer and preferably also introduces hydroxyl groups, e.g., diol moieties, (or derivatives thereof such as ester groups) onto the unsaturated moieties of the elastomeric diene-based polymers or copolymers. This combination of materials which has been oxidized in-situ can then be co-precipitated to form a polymeric mixture which can be melt-molded into polyolefin materials of improved structural, thermal and mechanical properties with desirable impact resistance.

Abstract: A process for preparing an epoxidized ?-olefin/diene copolymer including the steps of contacting in a reaction medium a) copolymers of an ?-olefin and a diene, which copolymers contain at least one double bond in each diene-derived co-monomer, with b) a hydrogen peroxide epoxidizing agent, in the presence of a perfluorinated alcohol reaction solvent, and in the absence of any metal-containing epoxidation catalyst, under reaction conditions which promote formation of oxirane rings at the sites of the diene-derived co-monomer double bonds in the copolymeric precursor material.

Abstract: Disclosed are processes for preparing an epoxidized and/or hydroxylated ?-olefin/diene copolymer materials such as ethylene/dicyclopentadiene. These processes comprise contacting in a reaction medium a) a copolymeric precursor component with b) a hydrogen peroxide oxidizing agent, in the presence of alkyl-trioxorhenium-based catalyst, under certain reaction conditions. The copolymeric precursor component comprises copolymers of ?-olefins and dienes with these copolymers containing at least one double bond in each diene-derived comonomer. The reaction medium is maintained under reaction conditions which promote formation of oxirane rings at, and/or diol formation across, the sites of the diene-derived co-monomer double bonds in the copolymeric precursor material. Epoxidation and hydroxylation generally increases the glass transition temperature, Tg, of these copolymers and imbues polarity which imparts oil resistance.

Abstract: A polymer composition comprises (a) greater than 50 wt % (based upon the weight of the composition) of a cyclic olefin copolymer comprising at least one acyclic olefin and at least 20 weight % of one or more cyclic olefins (based upon the weight of the cyclic olefin copolymer), wherein at least a portion of the cyclic olefin copolymer has a glass transition temperature of greater than 150° C.; and (b) less than 50 wt % (based upon the weight of the composition) of an acyclic olefin polymer modifier, at least a portion of the modifier having a glass transition temperature of less than ?30° C.; and no portion of the modifier having a softening point greater than +30° C., wherein the Bicerano solubility parameter of the modifier being no more than 0.6 J0.5/cm1.5 less than the Bicerano solubility parameter of the cyclic olefin copolymer. The polymer composition has a notched Izod impact resistance measured at 23° C. of greater than 500 J/m and a heat distortion temperature measured using a 0.

Abstract: Disclosed is a selected type of copolymer composition comprising copolymers having units derived from ethylene and dicyclopentadiene (DCPD) co-monomers. Such copolymer compositions: a) have a DCPD-derived comonomer unit content of from about 25 mole % to about 45 mole %; b) have a Weight Average Molecular Weight, Mw, of greater than about 170,000; c) comprise amorphous material and have glass transition temperatures, Tg, of from about 8° C. to about 129° C., which also fit the equation Tg (in ° C.)?[(mole % DCPD×3.142)?4.67]; and d) comprise no significant amount of crystalline polyethylene homopolymer or crystallizable polyethylene segments within the ethylene-dicylopentadiene copolymers. Such copolymers can be readily derivatized by hydrogention and/or epoxidation to provide polymeric materials suitable for use as engineering thermoplastics. Also disclosed are processes for preparing and optionally further derivatizing ethylene/dicyclopentadiene copolymers having the characteristics hereinbefore described.