Abstract: A microporous polyolefin membrane comprising a polyethylene resin, and polypropylene having a weight-average molecular weight of 6×105 or more and a heat of fusion of 90 J/g or more (measured by a differential scanning calorimeter), a fraction having a molecular weight of 1.8×106 or more being 10% or more by mass of the polypropylene.

Abstract: This invention is directed to processes of making polymer in the presence of a hydrofluorocarbon or perfluorocarbon and recovering the polymer. The processes provided enable polymerization processes to be practiced with minimal fouling in the reaction system, and to the recovery of the hydrofluorocarbon and other hydrocarbons such as hydrocarbons for reuse in the process or hydrocarbon by-products from the polymerization process. The invention is particularly beneficial in the production of ethylene based polymers using Ziegler Natta catalyst systems.

Abstract: This invention relates to a catalyst system comprising a catalyst and a support comprising a non-layered inorganic porous crystalline phase material, wherein the support comprises a hexagonal arrangement of uniformly-sized pores having an average pore diameter greater than or equal to about 13 ?, an X-ray diffraction pattern having a calculated d100 value of greater than or equal to about 18 ?, an adsorption capacity of greater than or equal to about 15 grams benzene per 100 grams support at 50 torr and at 25° C., and a pore wall thickness of less then or equal to about 25 ?.

Abstract: This invention is directed to a polymerization process that is carried out at relatively high productivity levels and with relatively low fouling. The process includes mixing together a catalyst system, at least one monomer and a hydrofluorocarbon to produce the polymer. The reaction is carried out such that little to no chlorine containing hydrocarbons are present.

Abstract: This invention relates to a process to polymerize olefins comprising contacting, in a reactor, a pyridyl-di-imine compound and an activator with one or more olefin monomer(s) in the presence of a fluorinated hydrocarbon.

Abstract: This invention relates to a process of polymerizing ethylene in a reactor comprising contacting a catalyst system comprising a supported chromium catalyst and an aluminum alkyl cocatalyst, where the catalyst and cocatalyst are contacted by cofeeding the catalyst and cocatalyst to the reactor or feeding the catalyst and cocatalyst separately to the reactor, where the catalyst and cocatalyst are not contacted prior to the step of feeding or cofeeding, with ethylene, and from 0 to 50 mole % of one or more comonomers, where the polymerization occurs at a temperature between 50 and 120° C., and the molar ratio of aluminum from the cocatalyst to the chromium in the supported chromium catalyst is 30:1 or more.

Abstract: Copolymerization of Ni(H) or Co(II) acenaphthene diimine complexes containing olefinic substituents on aryl groups in the presence of a free radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: This invention relates to a catalyst system comprising a catalyst and a support comprising a non-layered inorganic porous crystalline phase material, wherein the support comprises a hexagonal arrangement of uniformly-sized pores having an average pore diameter greater than or equal to about 13 ?, an X-ray diffraction pattern having a calculated d100 value of greater than or equal to about 18 ?, an adsorption capacity of greater than or equal to about 15 grams benzene per 100 grams support at 50 torr and at 25° C., and a pore wall thickness of less then or equal to about 25 ?.

Abstract: This invention relates to a catalyst system comprising a catalyst and a support comprising a non-layered inorganic porous crystalline phase material, wherein the support comprises a hexagonal arrangement of uniformly-sized pores having an average pore diameter greater than or equal to about 13 ?, an X-ray diffraction pattern having a calculated d100 value of greater than or equal to about 18 ?, an adsorption capacity of greater than or equal to about 15 grams benzene per 100 grams support at 50 torr and at 25° C., and a pore wall thickness of less then or equal to about 25 ?.

Abstract: Copolymerization of Ni(II) phenol imine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: Polymerization processes are disclosed for producing polyethylene having a target density and improved environmental stress resistance. Ethylene and optionally one or more ?-olefin comonomers, supported chromium catalyst, and metal alkyl cocatalyst are contacted to produce polyethylene. The density of the polyethylene is determined, and the concentration of cocatalyst is adjusted in response to a deviation between the density of the polyethylene and the target density. The catalyst and cocatalyst can be fed separately into the reactor, or can be co-fed, eliminating the need to pre-contact the catalyst and cocatalyst prior to introducing them into the reactor.

Abstract: This invention relates to a catalyst system comprising a catalyst and a support comprising a non-layered inorganic porous crystalline phase material, wherein the support comprises a hexagonal arrangement of uniformly-sized pores having an average pore diameter greater than or equal to about 13 ?, an X-ray diffraction pattern having a calculated d100 value of greater than or equal to about 18 ?, an adsorption capacity of greater than or equal to about 15 grams benzene per 100 grams support at 50 torr and at 25° C., and a pore wall thickness of less then or equal to about 25 ?.

Abstract: This invention relates to a process of polymerizing ethylene in a reactor comprising contacting a catalyst system comprising a supported chromium catalyst and an aluminum alkyl cocatalyst, where the catalyst and cocatalyst are contacted by cofeeding the catalyst and cocatalyst to the reactor or feeding the catalyst and cocatalyst separately to the reactor, where the catalyst and cocatalyst are not contacted prior to the step of feeding or cofeeding, with ethylene, and from 0 to 50 mole % of one or more comonomers, where the polymerization occurs at a temperature between 50 and 120° C., and the molar ratio of aluminum from the cocatalyst to the chromium in the supported chromium catalyst is 30:1 or more.

Abstract: An olefin polymerization catalyst system, comprising a catalyst represented by the general formula CrR4, wherein each R is independently a hydrocarbyl or substituted hydrocarbyl, with the proviso that R may not be a cyclopentadienyl group, an activator represented by the general formula, MQ2, where M is a Group II metal, where each Q is independently an alkyl, or substituted alkyl; and a support. The support may be organic or inorganic. Ethylene and one or more olefins may be polymerized by the catalyst system.

Abstract: Copolymerization of Fe(II) or Co(II) pyridine diimine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: An olefin polymerization catalyst system, comprising a catalyst represented by the general formula CrR4, wherein each R is independently a hydrocarbyl or substituted hydrocarbyl, with the proviso that R may not be a cyclopentadienyl group, an activator represented by the general formula, MQ2, where M is a Group II metal, where each Q is independently an alkyl, or substituted alkyl; and a support. The support may be organic or inorganic. Ethylene and one or more olefins may be polymerized by the catalyst system.

Abstract: Free-radical-initiated copolymerization of metallocene complexes containing olefinic substituents on aryl groups with styrene results in polymerized late transition metal catalysts that can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: Copolymerization of Ni(II) phenol imine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: Copolymerization of Ni(II) or Co(II) acenaphthene imine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: Polymerization processes are disclosed for producing polyethylene having a target density and improved environmental stress resistance. Ethylene and optionally one or more &agr;-olefin comonomers, supported chromium catalyst, and metal alkyl cocatalyst are contacted to produce polyethylene. The density of the polyethylene is determined, and the concentration of cocatalyst is adjusted in response to a deviation between the density of the polyethylene and the target density. The catalyst and cocatalyst can be fed separately into the reactor, or can be co-fed, eliminating the need to pre-contact the catalyst and cocatalyst prior to introducing them into the reactor.