A process for the production of alkyl ethers including feeding a hydrocarbon feedstock and a first alcohol feedstock to a fixed bed reactor containing an etherification catalyst. The hydrocarbon feedstock and the first alcohol feedstock are contacted in the first fixed bed reactor to react the isoolefins with the alcohol in the presence of the etherification catalyst to produce a first product stream. The first product stream is fed together with a hydrogen feedstock and a second alcohol feedstock to a catalytic distillation reaction system containing a trifunctional catalyst to concurrently isomerize at least a portion of the alpha-olefins, hydrogenate at least a portion of the diolefins, and etherify at least a portion of the isoolefins and alcohol, producing a bottoms product comprising the one or more ethers and an overhead product comprising n-alkanes, isoalkanes, unreacted alpha-olefins, unreacted internal-olefins, unreacted isoolefins, and unreacted alcohol.

Processes for producing alcohols from biomass are provided. The processes utilize supercritical methanol to depolymerize biomass with subsequent conversion to a mixture of alcohols. In particular the disclosure relates to continuous processes which produce high yields of alcohols through recycling gases and further employ dual reactor configurations which improve overall alcohol yields. Processes for producing higher ethers and olefins from the so-formed alcohols, through alcohol coupling and subsequent dehydration are also provided. The resulting distillate range ethers and olefins are useful as components in liquid fuels, such as diesel and jet fuel.

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

A process for producing xylenes, in particular para-xylene that is less energy intensive than conventional processes is provided. In an embodiment the process comprises contacting a feed mixture in an isomerization zone with a catalyst at isomerization conditions and producing an isomerized product comprising a higher proportion of p-xylene than in the feed mixture, wherein the catalyst comprises an acidic sulfonated catalytic membrane. Xylene isomerization can also be coupled with a p-xylene extraction process, where the raffinate (p-xylene deprived stream) from the extraction process is fed to an isomerization reactor to produce p-xylene. In an embodiment, the process can comprise: a) providing a feed stream comprising a mixture of xylene isomers including p-xylene; b) extracting p-xylene from the feed stream using a separator to separate the feed stream into a p-xylene rich stream and a p-xylene deprived stream; and c) delivering the p-xylene deprived stream to an isomerization unit, the isomerization unit including an acidic sulfonated catalytic membrane, and using the isomerization unit to produce an isomerized product comprising a higher proportion of p-xylene than in the p-xylene deprived stream delivered to the isomerization unit. In any one or more aspects, the isomerization unit can be operated at a temperature in the range of less than 350°, for example about 20° C. to about 200° C.

The invention relates to a method for preparing a cosmetic composition comprising the preparation of isododecane of natural origin and the mixture of isododecane formed with at least one compound selected from among: waxes, oils, film-forming agents, dyes and mixtures thereof. The invention also relates to the resulting cosmetic composition.

The present invention relates to a method for the oligomerization of ethylene, and more specifically, to a method for the preparation of mainly ethylene oligomers of C.sub.10 or higher, which comprises obtaining mainly ethylene oligomers of C.sub.4 or higher by performing a first oligomerization of an ethylene gas using a Ni-containing mesoporous catalyst, followed by a second oligomerization using an ion exchange resin, etc. The method for the preparation of ethylene oligomers according to the present invention can produce C.sub.8-16 ethylene oligomers in high yield without inducing inactivation of a catalyst, compared to the conventional technology of ethylene oligomerization by a one-step process.

Acyclic monterpene alcohols, like linalool, to be converted through a series of highly efficient catalytic reactions a biogasoline blending component, and a drop-in biodiesel fuel.

The selective dimerization of isoolefins, such as isobutene or isopentane, or mixtures thereof, may be conducted in a system including a series of fixed bed reactors and a catalytic distillation reactor. The system may provide for conveyance of the fixed bed reactor effluents, without componential separation, to a downstream reactor. It has been found that a high selectivity to the dimer may be achieved even though intermediate separation of the desired product from unreacted components between reactors is not performed. Further, embodiments provide for use of a divided wall column for recovery of a high purity dimer product, reducing unit piece count and plot size.

A method for producing p-xylene, comprising: a dimerization step of bringing a first raw material comprising isobutene into contact with a dimerization catalyst to generate C8 components comprising diisobutylene; a cyclization step of bringing a second raw material comprising the C8 components into contact with a dehydrogenation catalyst comprising Pt in the presence of water to obtain a reaction product comprising p-xylene; and a collection step of collecting p-xylene from the reaction product.

The selective dimerization of isoolefins, such as isobutene or isopentane, or mixtures thereof, may be conducted in a system including a series of fixed bed reactors and a catalytic distillation reactor. The system may provide for conveyance of the fixed bed reactor effluents, without componential separation, to a downstream reactor. It has been found that a high selectivity to the dimer may be achieved even though intermediate separation of the desired product from unreacted components between reactors is not performed. Further, embodiments provide for use of a divided wall column for recovery of a high purity dimer product, reducing unit piece count and plot size.