An apparatus for preparing polyalpha-olefins includes a mixing unit, a microchannel reaction unit, a high-pressure separation unit, a low-pressure separation unit, a gas circulation unit, a post-treatment unit and a pressure control unit, the mixing unit, the microchannel reaction unit, the high-pressure separation unit, the low-pressure separation unit that are successively connected. The gas circulation unit, the microchannel reaction unit is provided with the BF.sub.3 gas inlet, the mixing unit is provided with the auxiliary feed inlet, and the olefin raw material inlet, the gas circulation unit is connected with the BF.sub.3 gas inlet, the low-pressure separation unit is further connected with the post-treatment unit, and the high-pressure separation unit, the pressure control unit, and the gas circulation unit are further successively connected. The apparatus has the advantages of high polymerization reaction speed, high reaction conversion and good product selectivity, and is suitable for large-scale industrial production.

Embodiments of the present invention relates to integrated catalyst systems and associated processes that directly converts carbon dioxide or carbohydrate to CO, methane, or other valuable chemicals at room temperature and atmospheric pressure, requiring no extra energy. The integrated catalyst systems are comprised of nitrogenous heterocyclic compounds and at least two metal elements, wherein one metal element needs to be active than the other one. The integrated catalyst systems can be applied to reduce carbon dioxide and carbohydrate at room temperature with considerable conversion efficiency. The reduction process involves the steps of: a) nitrogenous heterocyclic compounds performance as solvent/major catalyst, dual component as reducing agent / co-catalyst; b) introducing the above integrated catalysts into the reactor full of CO.sub.2 or carbohydrate, and keeping stirring the reacting system for 1 to 4 hours, without any illumination or heating; c) CO, methane, or other reduction product is achieved with a conversion efficiency of about 100%; d) the reduction products are gases, which can be directly separated from the system without any additional separation process or involving additional chemicals.

This disclosure relates to base stocks comprising a C28-C32 hydrocarbon fraction and optionally a C42-C48 hydrocarbon fraction produced by dimerization and trimerization of a linear C14 mono-olefin, a linear C16 mono-olefin, or a mixture thereof, in the presence of a Lewis acid, oil compositions comprising such base stock(s), and processes for making such base stocks.

This disclosure relates to base stocks comprising a C28-C32 hydrocarbon fraction and optionally a C42-C48 hydrocarbon fraction produced by dimerization and trimerization of a linear C14 mono-olefin, a linear C16 mono-olefin, or a mixture thereof, in the presence of a Lewis acid, oil compositions comprising such base stock(s), and processes for making such base stocks.

A composition comprising olefin oligomers of one or more olefin monomers, the olefin monomers comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof. A composition comprising substantially hydrogenated olefin oligomers, wherein the olefin oligomers are oligomers of one or more olefin monomers, the olefin monomers comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof. A process comprising a) contacting 1) a catalyst system and 2) a monomer feedstock comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof in a reaction zone; and b) forming olefin oligomers.

A composition comprising olefin oligomers of one or more olefin monomers, the olefin monomers comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof. A composition comprising substantially hydrogenated olefin oligomers, wherein the olefin oligomers are oligomers of one or more olefin monomers, the olefin monomers comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof. A process comprising a) contacting 1) a catalyst system and 2) a monomer feedstock comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof in a reaction zone; and b) forming olefin oligomers.

A composition comprising olefin oligomers of one or more olefin monomers, the olefin monomers comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof. A composition comprising substantially hydrogenated olefin oligomers, wherein the olefin oligomers are oligomers of one or more olefin monomers, the olefin monomers comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof. A process comprising a) contacting 1) a catalyst system and 2) a monomer feedstock comprising a branched C.sub.10 olefin monomer comprising i) 3-propyl-1-heptene, ii) 4-ethyl-1-octene, iii) 5-methyl-1-nonene, or iv) any combination thereof in a reaction zone; and b) forming olefin oligomers.

The present invention is a method for producing a fluorinated hydrocarbon represented by a structural formula (3), wherein an ether compound represented by a structural formula (1) and an acid fluoride represented by a structural formula (2) are brought into contact with each other in a hydrocarbon-based solvent, in the presence of a catalyst in which boron trifluoride is supported on a metal oxide: wherein R.sup.1 and R.sup.2 represent an alkyl group having 1 to 3 carbon atoms, R.sup.3 represents a hydrogen atom, a methyl group or an ethyl group, and R.sup.4 and R.sup.5 represent a methyl group or an ethyl group; and R.sup.1 and R.sup.2 may be bonded to each other to form a cyclic structure. Through the present invention, a method for industrially advantageously producing 2-fluorobutane is provided. ##STR00001##

The present invention relates to a process for preparing cyclohexane by isomerizing a hydrocarbon mixture (HM1) comprising methylcyclopentane (MCP) in the presence of a catalyst. The catalyst is preferably an acidic ionic liquid. The starting material used is a stream (S1) which originates from a steamcracking process. The hydrocarbon mixture (HM1) obtained from this stream (S1) in an apparatus for aromatics removal has a reduced aromatics content compared to stream (S1), and (HM1) may optionally also be (virtually) free of aromatics. Depending on the type and amount of the aromatics remaining in the hydrocarbon mixture (HM1), especially in the case that benzene is present, the isomerization may additionally be preceded by performance of a hydrogenation of (HM1). In addition, depending on the presence of other components of (HM1), further purification steps may optionally be performed prior to or after the isomerization or hydrogenation. High-purity (on-spec) cyclohexane is preferably isolated from the hydrocarbon mixture (HM2) obtained in the isomerization, the specifications being, for example, those applicable to the use of the cyclohexane for the preparation, known to those skilled in the art, of caprolactam.

A continuous mixing reactor has an outer shell having a cylindrical portion with a central section and two opposite conical end sections; a circulation tube within the shell so that an annular passage forms between the shell and the circulation tube; an impeller within and positioned adjacent to one end of the circulation tube; and heat exchange means penetrating the outer shell and extending into the end of the circulation tube opposite the impeller. The outer shell has a hydraulic head forming one end of the shell, a heat exchange medium header at the opposite end of the shell. The circulation tube nearer the heat exchange medium header terminates at or downstream from a tangential plane extending through the shell at the intersection of the central section and the conical end section of the cylindrical portion of shell. The reactor is useful in an alkylation process.