Process and apparatus for the conversion of hydrocarbons

US9963403B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9963403-B2
Application numberUS-201514872388-A
CountryUS
Kind codeB2
Filing dateOct 1, 2015
Priority dateOct 27, 2014
Publication dateMay 8, 2018
Grant dateMay 8, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A hydrocarbon conversion process is described. The process includes contacting in a reactor an inert gas with one or more catalyst compositions suitable for methylation of toluene and hydrogenation of phenol; contacting a reducing agent with the one or more catalyst compositions under conditions suitable for reducing metal oxide content of the catalyst composition; contacting at least part of toluene and/or benzene-containing with a oxygenate in the presence of the one or more catalyst compositions and under conditions effective to convert toluene to xylenes and produce a reactor effluent stream comprising para-xylene and having a lower concentration of phenol than the toluene-containing stream; separating at least one para-xylene-enriched stream from the reactor effluent stream; and separating from the at least one para-xylene enriched stream at least one toluene-enriched stream and at least one para-xylene-product stream. An apparatus for carrying out such a process is also described.

First claim

Opening claim text (preview).

What is claimed is: 1. A hydrocarbon conversion, comprising: a) contacting in at least a first reactor an inert gas with one or more catalyst compositions suitable for methylation of toluene and/or hydrogenation of phenol, wherein the one or more catalyst compositions comprise an alkylation catalyst and a phenol hydrogenation catalyst, and wherein the alkylation catalyst is located in a first zone of the first reactor proximate the reactor inlet and the hydrogenation catalyst is located in a second zone of the first reactor proximate the reactor inlet; b) contacting a reducing agent with the one or more catalyst compositions under suitable conditions to reduce the metal oxide content of the one or more catalyst compositions; c) contacting at least part of an aromatic hydrocarbon stream comprising ≥5.0 wt % toluene and/or benzene with a oxygenate in the presence of the alkylation catalyst and under conditions effective to convert toluene to xylenes and produce a reactor effluent stream comprising para-xylene and phenol; d) contacting the reactor effluent stream with the hydrogenation catalyst to convert at least a portion of the phenol in the reactor effluent stream to cyclohexanone; e) separating in a first separator at least one para-xylene-enriched stream from the reactor effluent stream; and f) separating in a second separator from the at least one para-xylene enriched stream at least one toluene-enriched stream and at least one para-xylene-product stream. 2. The method of claim 1 , further comprising separating in a third separator a primarily para-xylene containing stream and para-xylene depleted stream from the at least one para-xylene-product stream. 3. The method of claim 2 , further comprising g) contacting at least a portion of primarily para-xylene containing stream with a free radical under conditions effective to oxidize at least a portion of the para-xylene to produce an oxidized effluent having terephthalic acid therein; h) recovering terephthalic acid from the oxidized effluent. 4. The method of claim 3 , further comprising contacting the primarily para-xylene containing stream with a phenol adsorbent composition prior to contacting the at least a portion of the primarily para-xylene containing stream with the free radical. 5. The method of claim 2 , further comprising contacting the para-xylene depleted stream with a xylene isomerization catalyst under conditions effective to isomerize xylenes in the para-xylene depleted stream and produce an isomerized stream. 6. The method of claim 5 , wherein contacting the para-xylene depleted stream with a xylene isomerization catalyst under conditions effective to isomerize xylenes includes contacting in the liquid phase and/or contacting in the vapor phase isomerization conditions. 7. The method of claim 5 , further comprising recycling at least part of the isomerized stream to the first separator. 8. The method of claim 5 , further comprising contacting the primarily para-xylene containing stream with a phenol adsorbent composition prior to contacting the para-xylene depleted stream with a xylene isomerization catalyst. 9. The method of claim 1 , wherein passing an inert gas through the one or more catalyst compositions comprises passing nitrogen, argon, or a mixture thereof through the one or more catalyst compositions. 10. The method of claim 1 , wherein passing a reducing agent through the one or more catalyst compositions comprises passing a composition comprising molecular hydrogen through the one or more catalyst compositions. 11. The method of claim 1 , further comprising, prior to contacting at least part of a toluene-containing stream with the oxygenate, separating a feed stream comprising C 6+ aromatic hydrocarbons into at least the toluene-containing stream and a C 8 aromatic hydrocarbon-containing stream. 12. The method of claim 1 , further comprising at least one of: contacting the at least one para-xylene enriched stream with a phenol adsorbent composition upstream of the second separator; and contacting the at least one para-xylene-product stream with a phenol adsorbent composition upstream of the third separator. 13. The method of claim 1 , wherein the oxygenate comprises methanol. 14. A hydrocarbon conversion, comprising: a) contacting in at least a first reactor an inert gas with one or more catalyst compositions suitable for methylation of toluene and hydrogenation of phenol, wherein the one or more catalyst compositions comprise an alkylation catalyst and a phenol hydrogenation catalyst, and wherein the first reactor comprises first and second reactor beds, and the alkylation catalyst is located in a first reactor bed and the hydrogenation catalyst is located in a second reactor bed; b) contacting a reducing agent with the one or more catalyst compositions under suitable conditions to reduce the metal oxide content of the first catalyst composition; c) contacting at least part of an aromatic hydrocarbon stream comprising ≥5.0 wt % toluene and/or benzene with a oxygenate in the presence of the alkylation catalyst and under conditions effective to convert toluene to xylenes and produce a reactor effluent stream comprising para-xylene and phenol; d) contacting the reactor effluent stream with the hydrogenation catalyst to convert at least a portion of the phenol in the reactor effluent stream to cyclohexanone; e) separating in a first separator at least one para-xylene-enriched stream from the reactor effluent stream; and f) separating in a second separator from the at least one para-xylene enriched stream at least one toluene-enriched stream and at least one para-xylene-product stream. 15. The method of claim 14 , further comprising separating in a third separator a primarily para-xylene containing stream and para-xylene depleted stream from the at least one para-xylene-product stream. 16. The method of claim 15 , further comprising: g) contacting at least a portion of primarily para-xylene containing stream with a free radical under conditions effective to oxidize at least a portion of the para-xylene to produce an oxidized effluent having terephthalic acid therein; h) recovering terephthalic acid from the oxidized effluent; and i) contacting the primarily para-xylene containing stream with a phenol adsorbent composition prior to contacting the at least a portion of the primarily para-xylene containing stream with the free radical. 17. The method of claim 15 , further comprising at least one of: j) contacting the para-xylene depleted stream with a xylene isomerization catalyst under conditions effective to isomerize xylenes in the para-xylene depleted stream and produce an isomerized stream; and k) recycling at least part of the isomerized stream to the first separator. 18. The method of claim 17 , further comprising contacting the primarily para-xylene containing stream with a phenol adsorbent composition prior to contacting the para-xylene depleted stream with a xylene isomerization catalyst. 19. The method of claim 14 , wherein passing an inert gas through the one or more catalyst compositions and the dehydrogenation catalyst comprises passing nitrogen, argon, or a mixture thereof through the one or more catalyst compositions. 20. The method of claim 14 , wherein passing a reducing agent through the one or more catalyst compositions comprises passing a composition comprising molecular hydrogen through the one or more catalyst compositions. 21. The method of claim 15 , further comprising contacti

Assignees

Inventors

Classifications

  • by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers · CPC title

  • C07C2/864Primary

    the non-hydrocarbon is an alcohol · CPC title

  • Xylenes · CPC title

  • by hydrogenation of aromatic hydroxy compounds · CPC title

  • Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously · CPC title

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What does patent US9963403B2 cover?
A hydrocarbon conversion process is described. The process includes contacting in a reactor an inert gas with one or more catalyst compositions suitable for methylation of toluene and hydrogenation of phenol; contacting a reducing agent with the one or more catalyst compositions under conditions suitable for reducing metal oxide content of the catalyst composition; contacting at least part of t…
Who is the assignee on this patent?
Exxonmobil Chemical Patents Inc
What technology area does this patent fall under?
Primary CPC classification C07C2/864. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).