Embodiments are directed to catalyst systems comprising at least one metal ligand complex and to processes for polyolefin polymerization incorporating the catalyst systems. The metal ligand complexes have the following structures: (I) ##STR00001##

This disclosure relates to ethylene interpolymer compositions and films prepared therefrom. Specifically: ethylene interpolymer products having: a dimensionless Long Chain Branching Factor, LCBF, greater than or equal to 0.001; a residual catalytic metal of from ≥0.03 to ≤5 ppm of hafnium, and; a dimensionless unsaturation ratio, UR, of from ≥−0.40 to ≤0.06, wherein UR is defined by the following relationship; UR=(SC.sup.U−T.sup.U)/T.sup.U, where SC.sup.U is the amount of a side chain unsaturation per 100 carbons and T.sup.U is amount of a terminal unsaturation per 100 carbons, in said ethylene interpolymer product. The disclosed ethylene interpolymer products have a melt index from about 0.3 to about 500 dg/minute, a density from about 0.855 to about 0.975 g/cc, a polydispersity (M.sub.w/M.sub.n) from about 1.7 to about 25 and a Composition Distribution Breadth Index (CDBI.sub.50) from about 1% to about 98%.

This disclosure relates to ethylene interpolymer compositions and films prepared therefrom. Specifically: ethylene interpolymer products having: a dimensionless Long Chain Branching Factor, LCBF, greater than or equal to 0.001; a residual catalytic metal of from ≥0.03 to ≤5 ppm of hafnium, and; a dimensionless unsaturation ratio, UR, of from ≥−0.40 to ≤0.06, wherein UR is defined by the following relationship; UR=(SC.sup.U−T.sup.U)/T.sup.U, where SC.sup.U is the amount of a side chain unsaturation per 100 carbons and T.sup.U is amount of a terminal unsaturation per 100 carbons, in said ethylene interpolymer product. The disclosed ethylene interpolymer products have a melt index from about 0.3 to about 500 dg/minute, a density from about 0.855 to about 0.975 g/cc, a polydispersity (M.sub.w/M.sub.n) from about 1.7 to about 25 and a Composition Distribution Breadth Index (CDBI.sub.50) from about 1% to about 98%.

A system and method of producing polyethylene, including: polymerizing ethylene in presence of a catalyst system in a reactor to form polyethylene, wherein the catalyst system includes a first catalyst and a second catalyst; and adjusting reactor conditions and an amount of the second catalyst fed to the reactor to control melt index (MI), density, and melt flow ratio (MFR) of the polyethylene.

A system and method of producing polyethylene, including: polymerizing ethylene in presence of a catalyst system in a reactor to form polyethylene, wherein the catalyst system includes a first catalyst and a second catalyst; and adjusting reactor conditions and an amount of the second catalyst fed to the reactor to control melt index (MI), density, and melt flow ratio (MFR) of the polyethylene.

Disclosed are a spherelike supermacroporous mesoporous material, a polyolefin catalyst, and a preparation method therefor and an olefin polymerization process. The spherelike supermacroporous mesoporous material has a twodimensional hexagonal ordered pore channel structures. The mesoporous material has an average pore size of 10 nm to 15 nm, a specific surface area of 300 m.sup.2/g to 400 m.sup.2/g, and an average particle size of 1 .Math.m to 3 .Math.m, based on the total mass of the mesoporous material. The mass content of water in the mesoporous material is < 1 ppm. The mass content of oxygen in the mesoporous material is < 1 ppm. When a polyolefin catalyst prepared with the mesoporous material as a carrier is used for an olefin polymerization reaction, the a polyolefin product with a narrow molecular weight distribution and a good melt index can be obtained.

Disclosed are a spherelike supermacroporous mesoporous material, a polyolefin catalyst, and a preparation method therefor and an olefin polymerization process. The spherelike supermacroporous mesoporous material has a twodimensional hexagonal ordered pore channel structures. The mesoporous material has an average pore size of 10 nm to 15 nm, a specific surface area of 300 m.sup.2/g to 400 m.sup.2/g, and an average particle size of 1 .Math.m to 3 .Math.m, based on the total mass of the mesoporous material. The mass content of water in the mesoporous material is < 1 ppm. The mass content of oxygen in the mesoporous material is < 1 ppm. When a polyolefin catalyst prepared with the mesoporous material as a carrier is used for an olefin polymerization reaction, the a polyolefin product with a narrow molecular weight distribution and a good melt index can be obtained.

An ethylene copolymer comprising ethylene and at least one alpha olefin having from 4 to 8 carbon atoms has a density f from 0.940 to 0.960 g/cm.sup.3, a molecular weight distribution, Mw/Mn of from 9 to 12, and a Z-average molecular weight, Mz of greater than 500,000. The ethylene copolymer is made in a multi-zone reactor system under solution phase polymerization conditions and is useful in the preparation of biaxially oriented polyethylene (BOPE) films.

An ethylene copolymer comprising ethylene and at least one alpha olefin having from 4 to 8 carbon atoms has a density f from 0.940 to 0.960 g/cm.sup.3, a molecular weight distribution, Mw/Mn of from 9 to 12, and a Z-average molecular weight, Mz of greater than 500,000. The ethylene copolymer is made in a multi-zone reactor system under solution phase polymerization conditions and is useful in the preparation of biaxially oriented polyethylene (BOPE) films.

The present disclosure relates to a Ziegler-Natta catalyst system comprising a pro-catalyst, a co-catalyst and a selectivity control agent. The pro-catalyst comprises a magnesium compound, a titanium compound and a multi-dentate internal donor, wherein the internal donor is tetraethyl 3,3,3′,3′-tetramethyl-2,2′,3,3′-tetrahydro-1,1′-spirobiindane-5,5′,6,6′-tetracarbonate. The present disclosure further relates to a process for polymerization of an olefin using the Ziegler-Natta catalyst system. The Ziegler-Natta catalyst system of the present disclosure shows very high hydrogen response and thus can be used to produce low to high molecular weight polyolefin.