C07C2523/883

Method for producing conjugated diolefin

A method for producing a conjugated diolefin is configured as follows. A monoolefin having four or more carbon atoms is fed from a plurality of monoolefin feed nozzles. In addition, at least 50% or more of a total amount of an oxygen-containing gas is fed from an oxygen-containing gas feed nozzle located at a bottom of a fluidized bed reactor. Furthermore, the plurality of monoolefin feed nozzles at n places located at heights a1, a2, . . . , and an from the oxygen-containing gas feed nozzle, respectively, feed the monoolefin having four or more carbon atoms at ratios of b1, b2, . . . , bn (b1+b2+ . . . +bn=1), respectively. Furthermore, a weighted mean value represented by the following formula is 100 mm or greater:
weighted mean value=a1*b1+a2*b2+ . . . +an*bn.

EVEN CARBON NUMBER PARAFFIN COMPOSITION AND METHOD OF MANUFACTURING SAME

Paraffin compositions including mainly even carbon number paraffins, and a method for manufacturing the same, is disclosed herein. In one embodiment, the method involves contacting naturally occurring fatty acid/glycerides with hydrogen in a slurry bubble column reactor containing bimetallic catalysts with equivalent particle diameters from about 10 to about 400 micron. The even carbon number compositions are particularly useful as phase change material.

Production process of 1,3-butadiene

A process of producing 1,3-butadiene includes: a first step of obtaining gases containing 1,3-butadiene by an oxidative dehydrogenation reaction of a raw material gas with a molecular oxygen-containing gas in the presence of a metal oxide catalyst, the raw material gas containing 1-butene and 2-butene and having a proportion of 2-butene to a sum of 1-butene and 2-butene, which is defined as 100% by volume, being not less than 50% by volume; a second step of cooling the produced gases obtained in the first step; and a third step of separating the produced gases having undergone the second step into molecular oxygen and inert gases and other gases containing 1,3-butadiene by selective absorption to an absorbing solvent, wherein the concentration of methyl vinyl ketone in the produced gases having been cooled in the second step is 0% by volume or more and not more than 0.03% by volume.

Process for reducing unsaturated hydrocarbons in aromatic fraction through selective hydrogenation

Disclosed are a process and system that are capable of performing selective hydrogenation on aromatic fractions by configuring a catalyst bed through staged loading of a plurality of hydrogenation catalysts with different catalytic properties, or configuring a catalyst system in which a plurality of hydrogenation catalysts are arranged using a plurality of reactors in such a way as to be equivalent with the staged loading, and as a result, are capable of suppressing aromatic loss while improving the selective removal of unsaturated hydrocarbons in the aromatic fraction and durability compared to the case of using a single catalyst.

METHOD FOR PRODUCING 1,3-BUTADIENE

The present invention has as its object the provision of a method for producing 1,3-butadiene capable of efficiently purifying an absorption solvent while a high productivity is assured.

A method for producing 1,3-butadiene includes: a step (A) of obtaining a produced gas containing 1,3-butadiene; a step (B) of cooling the produced gas; a step (C) of separating the produced gas, which has been subjected to the step (B); a step (D1) of separating the absorption solvent, that has absorbed an absorption component comprising the other gases containing 1,3 -butadiene into an absorption solvent that does not substantially contain the absorption component and an absorption solvent that contains the absorption component; a step (D2) of separating the absorption solvent that contains the absorption component into an absorption solvent that contains a reaction by-product and a 1,3-butadiene liquid; and a step (E) of purifying the absorption solvent, that contains the reaction by-product.

COUPLING OF UNIT FOR EXTRACTING METHYL-SUBSTITUTED AROMATICS WITH UNIT FOR HYDROGENOLYSING ALKYL-AROMATICS

The present invention relates to a device and a process for converting aromatic compounds, wherein: methyl-substituted aromatic compounds are extracted from a hydrocarbon feedstock (2) comprising aromatic compounds having at least 8 carbon atoms in an extraction unit (1), to produce at least one effluent enriched in methyl-substituted aromatic compounds (3A, 3B) and an effluent depleted in methyl-substituted aromatic compounds (4); and C2+ alkyl chains of the aromatic compounds of the depleted effluent (4) are converted into methyl groups in a hydrogenolysis unit (5) placed downstream of the extraction unit (1), to produce a hydrogenolysis effluent enriched in methyl-substituted aromatic compounds (7).

SELECTIVE HYDROXYL GROUP REMOVAL FROM ALKYLPHENOLS

A process for selective removal of hydroxyl groups from phenolic compounds is disclosed. The process uses a combination of catalytic hydrodeoxygenation and catalytic direct deoxygenation to convert alkylphenols into alkylbenzenes.

METHODS AND SYSTEMS FOR UPGRADING CRUDE OILS, HEAVY OILS, AND RESIDUES

Systems and methods for producing olefins and/or aromatics are disclosed. Methods disclosed includes aqua-processing hydro-processing of crude oils and/or heavy oils and/or residue, in an aqua-processing hydro-processing unit, to produce intermediate products, which can then be used to make valuable chemicals such as olefins and aromatics.

Process for Reducing Unsaturated Hydrocarbons in Aromatic Fraction Through Selective Hydrogenation
20220073440 · 2022-03-10 ·

Disclosed are a process and system that are capable of performing selective hydrogenation on aromatic fractions by configuring a catalyst bed through staged loading of a plurality of hydrogenation catalysts with different catalytic properties, or configuring a catalyst system in which a plurality of hydrogenation catalysts are arranged using a plurality of reactors in such a way as to be equivalent with the staged loading, and as a result, are capable of suppressing aromatic loss while improving the selective removal of unsaturated hydrocarbons in the aromatic fraction and durability compared to the case of using a single catalyst.

Even carbon number paraffin composition and method of manufacturing same

Paraffin compositions including mainly even carbon number paraffins, and a method for manufacturing the same, is disclosed herein. In one embodiment, the method involves contacting naturally occurring fatty acid/glycerides with hydrogen in a slurry bubble column reactor containing bimetallic catalysts with equivalent particle diameters from about 10 to about 400 micron. The even carbon number compositions are particularly useful as phase change material.