A process for the synthesis of a granular polymer, the process comprising (a) providing an active polymerization mixture that includes polymer, monomer, catalyst and optional solvent; (b) introducing a hydroxy-containing diaryl acetyl compound to the active polymerization mixture to thereby provide an inactive polymer mixture; (c) separating the polymer solution into a first stream and a second stream, where the first stream includes the polymer and the hydroxy-containing diaryl acetyl compound, and the second stream includes the monomer and the optional solvent; and (d) fabricating granules from the first stream.

A process for the synthesis of a granular polymer, the process comprising (a) providing an active polymerization mixture that includes polymer, monomer, catalyst and optional solvent; (b) introducing a hydroxy-containing diaryl acetyl compound to the active polymerization mixture to thereby provide an inactive polymer mixture; (c) separating the polymer solution into a first stream and a second stream, where the first stream includes the polymer and the hydroxy-containing diaryl acetyl compound, and the second stream includes the monomer and the optional solvent; and (d) fabricating granules from the first stream.

The present disclosure provides base stocks and processes for producing such basestocks by polymerizing internal olefins. The present disclosure further provides base stocks, comprising low molecular weight polyolefin products, having one or more of improved flow, low temperature properties, and thickening efficiency. The present disclosure further provides polyolefin products useful as base stocks and or diesel fuel. In at least one embodiment, a process includes introducing a feedstream comprising C.sub.4-C.sub.30 internal-olefins with a catalyst system comprising a nickel diimine catalyst optionally in the presence of a solvent. The method includes obtaining a C.sub.6-C.sub.100 polyolefin product having one or more of a carbon fraction of epsilon-carbons of from about 0.08 to about 0.3, as determined by .sup.13C NMR spectroscopy, based on the total carbon content of the polyolefin product.

The present disclosure provides base stocks and processes for producing such basestocks by polymerizing internal olefins. The present disclosure further provides base stocks, comprising low molecular weight polyolefin products, having one or more of improved flow, low temperature properties, and thickening efficiency. The present disclosure further provides polyolefin products useful as base stocks and or diesel fuel. In at least one embodiment, a process includes introducing a feedstream comprising C.sub.4-C.sub.30 internal-olefins with a catalyst system comprising a nickel diimine catalyst optionally in the presence of a solvent. The method includes obtaining a C.sub.6-C.sub.100 polyolefin product having one or more of a carbon fraction of epsilon-carbons of from about 0.08 to about 0.3, as determined by .sup.13C NMR spectroscopy, based on the total carbon content of the polyolefin product.

Method for the preparation of a composition enriched in 2-methyl-but-2-ene and use for making a polymer.

Method for the preparation of a composition enriched in 2-methyl-but-2-ene and use for making a polymer.

Metallocene complexes represented by the structure below are useful for alpha olefin oligomerization in the presence of an activator to generate polyalphaolefins having a high percentage of vinylidene termination and relatively low Mn values. ##STR00001##
M is a group 4 transition metal. A is a bridging group having one bridging atom extending between a first indenyl ring and a second indenyl ring. Each X is independently an anionic ligand, or two Xs are joined and bound to M to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand. R.sup.1, R.sup.1′, R.sup.3, R.sup.3′, R.sup.4, R.sup.4′, R.sup.7 and R.sup.7′ are hydrogen. R.sup.5, R.sup.5′, R.sup.6, and R.sup.6′ are independently a C.sub.1-C.sub.10, optionally substituted, hydrocarbyl group, or R.sup.5 and R.sup.6 and/or R.sup.5′ and R.sup.6′ are bonded together to form an optionally substituted hydrocarbyl ring structure.

Metallocene complexes represented by the structure below are useful for alpha olefin oligomerization in the presence of an activator to generate polyalphaolefins having a high percentage of vinylidene termination and relatively low Mn values. ##STR00001##
M is a group 4 transition metal. A is a bridging group having one bridging atom extending between a first indenyl ring and a second indenyl ring. Each X is independently an anionic ligand, or two Xs are joined and bound to M to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand. R.sup.1, R.sup.1′, R.sup.3, R.sup.3′, R.sup.4, R.sup.4′, R.sup.7 and R.sup.7′ are hydrogen. R.sup.5, R.sup.5′, R.sup.6, and R.sup.6′ are independently a C.sub.1-C.sub.10, optionally substituted, hydrocarbyl group, or R.sup.5 and R.sup.6 and/or R.sup.5′ and R.sup.6′ are bonded together to form an optionally substituted hydrocarbyl ring structure.

The present disclosure provides a process. In an embodiment, the process includes providing a purge stream containing octene monomer. The process includes contacting, under polymerization conditions, the purge stream with a bis-biphenylphenoxy catalyst, and forming an octene polymer having an absolute weight average molecular weight (Mw(Abs)) greater than 1,300,000 g/mol and a Mw(Abs)/Mn(Abs) from 1.3 to 3.0.

The present disclosure provides a process. In an embodiment, the process includes providing a purge stream containing octene monomer. The process includes contacting, under polymerization conditions, the purge stream with a bis-biphenylphenoxy catalyst, and forming an octene polymer having an absolute weight average molecular weight (Mw(Abs)) greater than 1,300,000 g/mol and a Mw(Abs)/Mn(Abs) from 1.3 to 3.0.