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35results about "Hydrocarbon by polyaryl split-off" patented technology

Method for directionally preparing benzene by utilizing xylogen

The invention relates to a method for directionally preparing benzene by utilizing xylogen. The method comprises the following steps of: selecting a cylindrical fixed bed catalytic reactor with a conductive metal wire arranged in a cavity; depolymerizing to converte xylogen to an aromatic monomer, wherein a led raw material is the xylogen, a catalyst is powder zeolite catalyst or modified zeolite catalyst containing transition metal nickel element, the usage amount is characterized in that the weight ratio of the catalyst to the xylogen is 0.3-10 per hour, and a product is a liquid-state aromatic monomer mixer; and directionally converting the aromatic monomer mixer into benzene, wherein a led raw material is the aromatic monomer mixer which is preheat to be 200-250 DEG C, a catalyst is powder zeolite catalyst containing an Re element, the usage amount is characterized in that the weight ratio of the aromatic monomer mixer to the zeolite catalyst containing the Re element is 0.2-15 per hour, and a product is mixed liquid taking the benzene as the main part. According to the method, an external hydrogen source is not needed, the raw material resources are rich, and higher benzene yield and benzene selectivity can be obtained at intermediate temperature and constant pressure as well as under a green and mild reaction environment.
Owner:UNIV OF SCI & TECH OF CHINA

Method for producing p-xylene employing diverse raw materials

The invention relates to a method for producing p-xylene employing diverse raw materials, and mainly aims at solving the problems of single raw material source and poor raw material adjustment flexibility in the prior art. The method comprises the following steps: feeding catalytically cracked light cycle oil to a selective hydrogenation open loop unit to generate a mixture I; introducing C5-C6 light dydrocarbons in the mixture I into a reforming unit together with reformate as reaction materials, and reacting to generate a mixture II; introducing C7-C10 in the mixture I into a transalkylation unit to react and generate a mixture III; feeding the mixtures II and III into a product separating unit, separating out C5-C6 components and returning to the reforming unit; returning the C7 component to the transalkylation unit, feeding C8 and the above components into a xylene tower; feeding C8 aromatics at the top of the xylene tower into a xylene adsorption unit to obtain a xylene product; and feeding components at the bottom of the tower into a heavy aromatic tower, separating out C9-C10 components and returning to the transalkylation unit. The problems are relatively well solved, and the method can be applied to industrial production of xylene.
Owner:CHINA PETROLEUM & CHEM CORP +1

Method for directionally preparing benzene by utilizing xylogen

The invention relates to a method for directionally preparing benzene by utilizing xylogen. The method comprises the following steps of: selecting a cylindrical fixed bed catalytic reactor with a conductive metal wire arranged in a cavity; depolymerizing to converte xylogen to an aromatic monomer, wherein a led raw material is the xylogen, a catalyst is powder zeolite catalyst or modified zeolite catalyst containing transition metal nickel element, the usage amount is characterized in that the weight ratio of the catalyst to the xylogen is 0.3-10 per hour, and a product is a liquid-state aromatic monomer mixer; and directionally converting the aromatic monomer mixer into benzene, wherein a led raw material is the aromatic monomer mixer which is preheat to be 200-250 DEG C, a catalyst is powder zeolite catalyst containing an Re element, the usage amount is characterized in that the weight ratio of the aromatic monomer mixer to the zeolite catalyst containing the Re element is 0.2-15 per hour, and a product is mixed liquid taking the benzene as the main part. According to the method, an external hydrogen source is not needed, the raw material resources are rich, and higher benzene yield and benzene selectivity can be obtained at intermediate temperature and constant pressure as well as under a green and mild reaction environment.
Owner:UNIV OF SCI & TECH OF CHINA

Catalytic hydrodearylation of heavy aromatic streams containing dissolved hydrogen with fractionation

ActiveUS20210139393A1Increase overall C6-C aromatics productionImprove blending suitabilityHydrocarbon by polyaryl split-offFractional condensation purification/separationArylPtru catalyst
Systems and methods for hydrodearylation of a hydrocarbon feed stream comprising non-condensed alkyl-bridged multi-aromatic hydrocarbons, the method including supplying a hydrogen feed to the hydrocarbon feed stream comprising non-condensed alkyl-bridged multi-aromatic hydrocarbons; mixing the hydrogen feed with the hydrocarbon feed stream to saturate the hydrocarbon feed stream with hydrogen gas to create a hydrogen-enriched liquid hydrocarbon stream; passing the hydrogen-enriched liquid hydrocarbon stream to a hydrodearylation reactor without a separate gaseous phase of hydrogen; allowing the hydrogen-enriched liquid hydrocarbon stream to react in presence of a catalyst under specific reaction conditions to produce a product stream comprising a reduced concentration of di-aromatic compounds and an increased concentration of mono-aromatic compounds compared to the hydrocarbon feed stream comprising non-condensed alkyl-bridged multi-aromatic hydrocarbons; and recovering, from the hydrodearylation reactor, a product stream for a downstream process, wherein the non-condensed alkyl-bridged multi-aromatic hydrocarbons include at least two benzene rings connected by an alkyl bridge group having at least two carbons, wherein the benzene rings are connected to different carbons of the alkyl bridge group.
Owner:SAUDI ARABIAN OIL CO

Catalytic hydrodearylation of heavy aromatic streams containing dissolved hydrogen with fractionation

Systems and methods for hydrodearylation of a hydrocarbon feed stream comprising non-condensed alkyl-bridged multi-aromatic hydrocarbons, the method including supplying a hydrogen feed to the hydrocarbon feed stream comprising non-condensed alkyl-bridged multi-aromatic hydrocarbons; mixing the hydrogen feed with the hydrocarbon feed stream to saturate the hydrocarbon feed stream with hydrogen gas to create a hydrogen-enriched liquid hydrocarbon stream; passing the hydrogen-enriched liquid hydrocarbon stream to a hydrodearylation reactor without a separate gaseous phase of hydrogen; allowing the hydrogen-enriched liquid hydrocarbon stream to react in presence of a catalyst under specific reaction conditions to produce a product stream comprising a reduced concentration of di-aromatic compounds and an increased concentration of mono-aromatic compounds compared to the hydrocarbon feed stream comprising non-condensed alkyl-bridged multi-aromatic hydrocarbons; and recovering, from the hydrodearylation reactor, a product stream for a downstream process, wherein the non-condensed alkyl-bridged multi-aromatic hydrocarbons include at least two benzene rings connected by an alkyl bridge group having at least two carbons, wherein the benzene rings are connected to different carbons of the alkyl bridge group.
Owner:SAUDI ARABIAN OIL CO

Method for producing norbornene derivative

A method for producing a norbornene derivative wherein,
    • in the presence of palladium and at least one selected from phosphorus compounds represented by the following General Formulae (1) and (2):
[in Formula (1), R1, R2, R3 and R4 each independently represent a hydrogen atom or the like, and R5 and R6 each independently represent a branched chain saturated hydrocarbon group having 3 to 10 carbon atoms or the like], and
[in Formula (2), R7 represents a branched chain saturated hydrocarbon group having 3 to 10 carbon atoms],
    • a norbornadiene derivative represented by the following General Formula (3):
[in Formula (3), R8, R9, R10, R11 and R12 each independently represent a hydrogen atom or the like, l represents an integer of 0 or 1, m represents an integer of 0 or 1, and n represents an integer of 0 or 1], and a bromine compound represented by the following General Formula (4):
[Chemical Formula 4]
Br—Z—R13  (4)
[in Formula (4), Z represents a phenylene group or the like, and R13 represents a hydrogen atom or the like] are reacted with each other, to thereby obtain a norbornene derivative represented by the following General Formula (5):
[in Formula (5), R14, R15, R16, R17 and R18 each independently represent a hydrogen atom or the like, Z represents a phenylene group or the like, R19 represents a hydrogen atom or the like, l represents an integer of 0 or 1, m represents an integer of 0 or 1, and n represents an integer of 0 or 1], the norbornene derivative having a configuration of a substituent represented by Z in General Formula (5) that is an exo configuration.
Owner:NIPPON OIL CORP
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