Patent classifications
C08F110/14
Toluene Free Preparation of SMAO: Heating with TMA to Improve Activity
A method including: contacting a support material including absorbed water with trimethylaluminum (TMA) in an aliphatic hydrocarbon; removing the aliphatic hydrocarbon by distillation at a pressure greater than or equal to 0.5 atm; heating, at a temperature ranging from about 25° C. to about 200° C., a reaction product of the support material and the TMA in a presence of TMA, wherein the TMA includes TMA in an amount of about 2-10 mmol TMA per gram of the support material in excess of an amount that reacts with the support material absorbed with water; and removing excess TMA.
Solubility Improvement of Non-Metallocene Transition Metal Complexes in Aliphatic Hydrocarbon Solvents
It has become desirable to limit or exclude aromatic solvents, such as toluene, from polymerization reactions. For polymerization reactions employing a non-metallocene transition metal complex as a precursor to a polymerization catalyst, exclusion of aromatic solvents may be difficult due to the limited solubility of such complexes in aliphatic hydrocarbon solvents. Aliphatic hydrocarbon solutions suitable for conducting olefin polymerization reactions, particularly solution polymerization reactions, may comprise: a non-metallocene transition metal complex dissolved in an aliphatic hydrocarbon solvent at a concentration ranging from about 2 mM to about 20 mM at 25° C. in the presence of an organoaluminum compound. A molar ratio of aluminum of the organoaluminum compound to transition metal of the transition metal complex is about 1:1 or greater, and the organoaluminum compound comprises at least about 8 carbons per aluminum.
METHOD OF CONTROLLING KINEMATIC VISCOSITY OF POLYALPHAOLEFIN
The invention relates to a method of the oligomerization of C6 and above olefin monomer whereby, at a fixed monomer/Al halide mole ratio, polyalphaolefins having desirable kinematic viscosities are prepared by controlling the oligomerization temperature. The oligomerization is carried out in presence of an oligomerizing catalyst comprising of aluminum halide and a promoter, and oligomerizing temperatures of about 10° C. to about 120° C.
METHOD OF CONTROLLING KINEMATIC VISCOSITY OF POLYALPHAOLEFIN
The invention relates to a method of the oligomerization of C6 and above olefin monomer whereby, at a fixed monomer/Al halide mole ratio, polyalphaolefins having desirable kinematic viscosities are prepared by controlling the oligomerization temperature. The oligomerization is carried out in presence of an oligomerizing catalyst comprising of aluminum halide and a promoter, and oligomerizing temperatures of about 10° C. to about 120° C.
Method of preparing a molecular catalyst
Method of preparing a molecular catalyst from a mixture comprising a (C.sub.5-C.sub.7)alkane, a spray-dried alkylaluminoxane, and a molecular procatalyst. Molecular catalysts prepared by the method may be screened.
Catalyst systems and processes for poly alpha-olefin having high vinylidene content
A process for making a poly alpha-olefin (PAO) having a relatively high vinylidene content (or combined vinylidene and tri-substituted vinylene content) and a relatively low vinyl and/or di-substituted vinylene content, as well as a relatively low molecular weight. The process includes: contacting a feed containing a C.sub.2-C.sub.32 alpha-olefin with a catalyst system comprising activator and a bis-cyclopentadienyl metallocene compound, typically a cyclopentadienyl-benzindenyl group 4 transition metal compound.
Catalyst systems and processes for poly alpha-olefin having high vinylidene content
A process for making a poly alpha-olefin (PAO) having a relatively high vinylidene content (or combined vinylidene and tri-substituted vinylene content) and a relatively low vinyl and/or di-substituted vinylene content, as well as a relatively low molecular weight. The process includes: contacting a feed containing a C.sub.2-C.sub.32 alpha-olefin with a catalyst system comprising activator and a bis-cyclopentadienyl metallocene compound, typically a cyclopentadienyl-benzindenyl group 4 transition metal compound.
Halogen-containing synthetic base oils, and preparation method and use thereof
The present invention provides a class of halogen-containing synthetic base oils, and preparation method and use thereof. The synthetic base oils have introduced with halogen, especially fluorine, wherein the dipole motion of the halogen groups results in dipole interaction between the dipoles of other components and the base oil molecules of dipole-dipole and dipole-induced halogen (especially fluorine), and the interaction force is stronger and more localized than the dispersion force between the molecules of pure hydrocarbon synthetic oils, and thus the performance of the base oils is directly affected. It solved the problem of oil solubility of pure hydrocarbon synthetic oils, and also improved the properties of oxidation resistance and thermal stability.
Halogen-containing synthetic base oils, and preparation method and use thereof
The present invention provides a class of halogen-containing synthetic base oils, and preparation method and use thereof. The synthetic base oils have introduced with halogen, especially fluorine, wherein the dipole motion of the halogen groups results in dipole interaction between the dipoles of other components and the base oil molecules of dipole-dipole and dipole-induced halogen (especially fluorine), and the interaction force is stronger and more localized than the dispersion force between the molecules of pure hydrocarbon synthetic oils, and thus the performance of the base oils is directly affected. It solved the problem of oil solubility of pure hydrocarbon synthetic oils, and also improved the properties of oxidation resistance and thermal stability.
Halogen-containing synthetic base oils, and preparation method and use thereof
The present invention provides a class of halogen-containing synthetic base oils, and preparation method and use thereof. The synthetic base oils have introduced with halogen, especially fluorine, wherein the dipole motion of the halogen groups results in dipole interaction between the dipoles of other components and the base oil molecules of dipole-dipole and dipole-induced halogen (especially fluorine), and the interaction force is stronger and more localized than the dispersion force between the molecules of pure hydrocarbon synthetic oils, and thus the performance of the base oils is directly affected. It solved the problem of oil solubility of pure hydrocarbon synthetic oils, and also improved the properties of oxidation resistance and thermal stability.