Process for producing a heterophasic propylene copolymer using a specific class of metallocene complexes in a multistage polymerization process including a gas phase polymerization step. The invention further relates to the use of catalysts which comprise a specific class of metallocene complexes to produce a heterophasic propylene copolymer in a multistep process including a gas phase polymerization step.

A method of producing bimodal ethylene-based polymer includes reacting ethylene monomer and C.sub.3-C.sub.12 α-olefin comonomer in the presence of a first catalyst in an agitated reactor to produce a first polymer fraction, and outputting effluent from the agitated reactor. A second catalyst is added to the effluent downstream of the agitated reactor and upstream from a non-agitated reactor, the second catalyst facilitates production of a second polymer fraction having a density and melt index (I.sub.2) different from the first polymer fraction. The second catalyst and effluent are mixed in at least one mixer. The second catalyst, second polymer fraction, and the first polymer fraction are passed to the non-agitated reactor; and additional ethylene monomer, additional C.sub.3-C.sub.12 α-olefin comonomer, and solvent are passed to the non-agitated reactor to produce more second polymer fraction and thereby the bimodal ethylene-based polymer.

Embodiments are directed to a catalyst system comprising metal-ligand complexes and processes for polyolefin polymerization using the metal-ligand complex having the following structure: ##STR00001##

The present disclosure provides catalyst compounds having an amine bridged anilide phenolate ligand. In at least one embodiment, catalysts of the present disclosure provide catalyst activity values of about 90 gP/mmolCat.Math.h.sup.−1 or greater and polyolefins, such as polyethylene copolymers, having comonomer content of from about 4 wt % to about 12 wt %, an Mn of about 90,000 g/mol or more, an Mw of 155,000 g/mol or more, and an Mw/Mn of from 1 to 2.5.

The disclosure provides a polymerization process for producing ethylene based polymers comprising polymerizing ethylene and optionally one or more α-olefins in the presence of a catalyst systems in a reactor system having one or more reactors, wherein the catalyst system comprises; (a) one or more procatalysts comprising a metal-ligand complex of formula (I) below: ##STR00001##

A multilayer blown film having an inner layer, a first outer layer, and a second outer layer, wherein the inner layer comprises an ethylene-based polymer having a MWCDI value greater than 0.9, and a melt index ratio (I10/I2) that meets the following equation: I10/I2≥7.0−1.2×log (I2); and the first outer layer and the second outer layer independently comprise a polyethylene composition which comprises the reaction product of ethylene and, optionally, one or more alpha olefin comonomers, wherein the polyethylene composition is characterized by the following properties: (a) a melt index, I.sub.2, of from 0.1 to 2.0 g/10 min; (b) a density of from 0.910 to 0.930 g/cc; (c) a melt flow ratio, I.sub.10/I.sub.2, of from 6.0 to 7.6; and (d) a molecular weight distribution, (Mw/Mn) of from 2.5 to 4.0.

A process to produce a branched ethylene-α-olefin diene elastomer comprising combining a catalyst precursor and an activator with a feed comprising ethylene, C3 to C12 α-olefins, and a dual-polymerizable diene to obtain a branched ethylene-α-olefin diene elastomer; where the catalyst precursor is selected from pyridyldiamide and quinolinyldiamido transition metal complexes. The branched ethylene-α-olefin diene elastomer may comprise within a range from 40 to 80 wt % of ethylene-derived units by weight of the branched ethylene-α-olefin diene elastomer, and 0.1 to 2 wt % of singly-polymerizable diene derived units, 0.1 to 2 wt % of singly-polymerizable diene derived units, and the remainder comprising C3 to C12 α-olefin derived units, wherein the branched ethylene-α-olefin diene elastomer has a weight average molecular weight (M.sub.w) within a range from 100 kg/mole to 300 kg/mole, an average branching index (g′.sub.avg) of 0.9 or more, and a branching index at very high M.sub.w (g′.sub.1000) of less than 0.9.

A homopolypropylene has i) a molecular weight distribution of less than 2.4; ii) a melt index (measured at 230° C. under a load of 2.16 kg in accordance with ASTM D1238) of 5 to 3000 g/10 min; iii) a remaining stress ratio of 0.5% or less; and iv) a complex viscosity of 5 to 600 Pa.Math.s at an angular frequency of 1 rad/s and a complex viscosity of 5 to 300 Pa.Math.s at an angular frequency of 100 rad/s. A method for preparing the homopolyproylene is also provided. A molded article and a non-woven fabric are also provided.

The present disclosure provides methods for producing an olefin polymer including: i) contacting alpha-olefin with a first catalyst system comprising a first non-metallocene catalyst, a first activator, and a reversible chain transfer agent to form a first polymer; ii) contacting the first polymer with a coupling agent in the presence of a catalyst, an activator; and iii) obtaining a second polymer. The present disclosure further provides polymers having a g′vis value from about 0.4 to about 0.8 and a vinyl unsaturation content of 0.8 or greater vinyls/1000 carbons, and preferably low gel content.

The present disclosure relates to Lewis base catalysts. Catalysts, catalyst systems, and processes of the present disclosure can provide high temperature ethylene polymerization, propylene polymerization, or copolymerization. In at least one embodiment, the catalyst compounds belong to a family of compounds comprising amido-phenolate-heterocyclic ligands coordinated to group 4 transition metals. The tridendate ligand may include a central neutral hetrocyclic donor group, an anionic phenolate donor, and an anionic amido donor. In some embodiments, the present disclosure provides a catalyst system comprising an activator and a catalyst of the present disclosure. In some embodiments, the present disclosure provides a polymerization process comprising a) contacting one or more olefin monomers with a catalyst system comprising: i) an activator and ii) a catalyst of the present disclosure.