C07C2531/10

ISOMERIZATION OF LINEAR OLEFINS WITH SOLID ACID CATALYSTS AND PRIMARY ESTERS
20240067589 · 2024-02-29 ·

Isomerized olefin products are produced by contacting an olefin feed containing a C.sub.10 to C.sub.20 normal alpha olefin, a solid acid catalyst, and a C.sub.2 to C.sub.15 primary ester to form the isomerized olefin product. Typical primary esters used in the processes include formates and acetates. Linear olefin compositions are produced that contain at least 80 wt. % C.sub.10 to C.sub.20 linear internal olefins, less than 8 wt. % C.sub.10 to C.sub.20 normal alpha olefins, less than 8 wt. % dimers of C.sub.10 to C.sub.20 olefins, less than 15 wt. % C.sub.10 to C.sub.20 branched olefins, and at least 1 wt. % C.sub.2 to C.sub.15 primary ester and less than 8 wt. % secondary esters.

METHODS FOR MAKING LINEAR INTERNAL OLEFINS FROM MIXTURES OF LINEAR AND BRANCHED OLEFINS
20240051900 · 2024-02-15 ·

Processes for producing a linear internal olefin product include the steps of contacting an olefin feed containing C.sub.10-C.sub.20 vinylidenes and a C.sub.10-C.sub.20 normal alpha olefin and/or C.sub.10-C.sub.20 linear internal olefins, a first acid catalyst, and a C.sub.1 to C.sub.18 carboxylic acid to form a first reaction product containing linear internal olefins, trisubstituted olefins, and secondary esters, then removing all or a portion of the secondary esters from the first reaction product, followed by contacting the secondary esters and a second acid catalyst to form a second reaction product comprising linear internal olefins, and then removing all or a portion of the linear internal olefins from the second reaction product to form the linear internal olefin product. Linear alkanes subsequently can be produced by hydrogenating the linear internal olefin product to form a linear alkane product.

Method and composition for contemporaneously dimerizing and hydrating a feed having butene to produce a gasoline composition

Methods for producing alcohols and oligomers contemporaneously from a hydrocarbon feed containing mixed butenes using an acid based catalyst are provided. Additionally, methods for producing fuel compositions having alcohols and oligomers prepared from mixed olefins are also provided as embodiments of the present invention. In certain embodiments, the catalyst can include a dual phase catalyst system that includes a water soluble acid catalyst and a solid acid catalyst.

Method for oligomerization of ethylene

Methods for the oligomerization of ethylene, and more specifically, methods for the preparation of mainly ethylene oligomers of C.sub.10 or higher are described. A method can include 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. to produce ethylene oligomers of C.sub.10 or higher. The method for the preparation of ethylene oligomers can produce C.sub.8-16 ethylene oligomers in high yield without inducing deactivation of the catalyst, compared to the conventional technology of ethylene oligomerization by a one-step process.

Upgrading 5-nonanone

Provided are fuel components, a method for producing fuel components, use of the fuel components and fuel containing the fuel components based on 5-nonanone.

Process for preparing perhydrofluorene or alkyl-substituted perhydrofluorene

The present invention discloses a process for preparing perhydrofluorene or alkyl-substituted perhydrofluorene, comprising the steps of: (1) reacting a phenolic compound or an aromatic hydrocarbon compound or an aromatic ketone compound or an aromatic ether compound with a benzyl compound to carry out an alkylation reaction in the presence of a first catalyst, thereby to produce substituted or unsubstituted diphenyl methane, wherein the first catalyst is an acidic catalyst; and (2) reacting the substituted or unsubstituted diphenyl methane with hydrogen gas to carry out an hydrogenation reaction or a hydrodeoxygenation reaction, thereby to produce perhydrofluorene or alkyl-substituted perhydrofluorene, wherein the second catalyst is a physical mixture of a metal catalyst and an acidic catalyst or a metal catalyst loaded on an acidic catalyst.

A Process for Preparing Perhydrofluorene or Alkyl-Substituted Perhydrofluorene
20190031576 · 2019-01-31 ·

The present invention discloses a process for preparing perhydrofluorene or alkyl-substituted perhydrofluorene, comprising the steps of: (1) reacting a phenolic compound or an aromatic hydrocarbon compound or an aromatic ketone compound or an aromatic ether compound with a benzyl compound to carry out an alkylation reaction in the presence of a first catalyst, thereby to produce substituted or unsubstituted diphenyl methane, wherein the first catalyst is an acidic catalyst; and (2) reacting the substituted or unsubstituted diphenyl methane with hydrogen gas to carry out an hydrogenation reaction or a hydrodeoxygenation reaction, thereby to produce perhydrofluorene or alkyl-substituted perhydrofluorene, wherein the second catalyst is a physical mixture of a metal catalyst and an acidic catalyst or a metal catalyst loaded on an acidic catalyst.

Methods for making linear internal olefins from mixtures of linear and branched olefins

Processes for producing a linear internal olefin product include the steps of contacting an olefin feed containing C.sub.10-C.sub.20 vinylidenes and a C.sub.10-C.sub.20 normal alpha olefin and/or C.sub.10-C.sub.20 linear internal olefins, a first acid catalyst, and a C.sub.1 to C.sub.18 carboxylic acid to form a first reaction product containing linear internal olefins, trisubstituted olefins, and secondary esters, then removing all or a portion of the secondary esters from the first reaction product, followed by contacting the secondary esters and a second acid catalyst to form a second reaction product comprising linear internal olefins, and then removing all or a portion of the linear internal olefins from the second reaction product to form the linear internal olefin product. Linear alkanes subsequently can be produced by hydrogenating the linear internal olefin product to form a linear alkane product.

Xylene isomerization

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.

Processes for producing poly alpha olefins and apparatuses therefor

The present disclosure provides processes and apparatus for producing poly alpha olefins. In at least one embodiment, a process to produce a poly alpha olefin includes introducing a first olefin monomer to a first catalyst and an activator in a first reactor to form a first reactor effluent comprising olefin dimers and olefin timers. The process includes heating the first reactor effluent to form an isomerized product and introducing the isomerized product to a filtration unit to form a filtration effluent. The process may include introducing the filtration effluent to a first distillation unit to form a first distillation effluent. The process may include introducing the first distillation effluent to a second distillation unit to form a second distillation effluent. The process includes introducing the first distillation effluent and/or the second distillation effluent to a second catalyst in a second reactor to form a second reactor effluent comprising the olefin timers.