Combined heavy reformate dealkylation-transalkylation process for maximizing xylenes production

US10071939B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10071939-B2
Application numberUS-201514636297-A
CountryUS
Kind codeB2
Filing dateMar 3, 2015
Priority dateApr 19, 2012
Publication dateSep 11, 2018
Grant dateSep 11, 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.

The present invention relates to a method of forming mixed xylenes from a heavy reformate using a dealkylation-transalkylation system that includes the step of introducing a heavy reformate containing methyl ethyl benzenes and tri-methyl benzenes and sufficiently free of toluene into the dealkylation stage with a hydrogen-containing material such that the heavy reformate and the hydrogen-containing material intermingle and contact a hydrodealkylation catalyst. The dealkylation-transalkylation system includes dealkylation stages, non-aromatic product gas separations and transalkylation stages. The BTEX component toluene forms from the reaction of methyl ethyl benzenes and hydrogen in the presence of the hydrodealkylation catalyst. The method also includes the step of introducing a dealkylated heavy reformate into the transalkylation stage such that the dealkylated heavy reformate contacts a transalkylation catalyst, forming a transalkylation stage product mixture that includes mixed xylenes.

First claim

Opening claim text (preview).

What is claimed is: 1. A dealkylation-transalkylation system that is useful for forming mixed xylenes from a heavy reformate that includes both methyl ethyl benzenes and tri-methyl benzenes comprising: a dealkylation stage that contains a hydrodealkylation catalyst, that is operable to receive both a hydrogen-containing material and the heavy reformate, and that is operable to produce a dealkylation stage product that contains toluene, tri-methyl benzenes and non-aromatic product gas; a non-aromatic product gas separations stage that is fluidly coupled to the dealkylation stage, that is operable to receive the dealkylation stage product, and that is operable to produce separately the non-aromatic product gas and a dealkylation heavy reformate that contains toluene and tri-methyl benzenes; and a transalkylation stage that is fluidly coupled to the non-aromatic product gas separations stage, that contains a transalkylation catalyst, that is operable to receive the dealkylation heavy reformate, and that is operable to produce a transalkylation stage product that contains mixed xylenes; a recycle loop that fluidly couples the dealkylation stage to the non-aromatic product gas separations stage and that is operable to convey hydrogen to the dealkylation stage; wherein the hydrodealkylation catalyst is operable to selectively convert methyl ethyl benzenes and hydrogen into toluene and the non-aromatic product gas; wherein the transalkylation catalyst is operable to selectively convert tri-methyl benzenes and toluene into mixed xylenes; wherein the hydrodealkylation catalyst and the transalkylation catalyst are not the same material, and wherein the hydrodealkylation catalyst and the transalkylation catalyst are not contained in the same stage. 2. The system of claim 1 , wherein the non-aromatic product gas separations stage and the dealkylation stage are part of the same vessel. 3. The system of claim 1 , further comprising a post-dealkylation-transalkylation refining system that fluidly couples to the transalkylation stage, that is operable to receive the transalkylation stage product and that is operable to produce a benzene product, a toluene product, a mixed xylenes product and a C9+ alkyl aromatics. 4. The system of claim 3 , further comprising a recycle loop that fluidly couples the dealkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey the C9+ alkyl aromatics to the dealkylation stage. 5. The system of claim 3 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the benzene product to the transalkylation stage. 6. The system of claim 3 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the toluene product to the transalkylation stage. 7. The system of claim 3 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the mixed xylene product to the transalkylation stage. 8. The system of claim 3 , where the post-dealkylation-transalkylation refining system is further operable to produce a para-xylene product, an ortho-xylene product and a meta-xylene product from the mixed xylenes. 9. The system of claim 8 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the meta-xylene product to the transalkylation stage. 10. The system of claim 1 , wherein the transalkylation stage comprises a fluidized catalyst bed. 11. The system of claim 1 , wherein the transalkylation stage comprises a moving catalyst bed. 12. A dealkylation-transalkylation system that is useful for forming mixed xylenes from a heavy reformate that includes both methyl ethyl benzenes and tri-methyl benzenes comprising: a dealkylation stage that contains a hydrodealkylation catalyst, that is operable to receive both a hydrogen-containing material and the heavy reformate, and that is operable to produce a dealkylation stage product that contains toluene, tri-methyl benzenes and non-aromatic product gas; a non-aromatic product gas separations stage that is fluidly coupled to the dealkylation stage, that is operable to receive the dealkylation stage product, and that is operable to produce separately the non-aromatic product gas and a dealkylation heavy reformate that contains toluene and tri-methyl benzenes; and a transalkylation stage that is fluidly coupled to the non-aromatic product gas separations stage, that contains a transalkylation catalyst, that is operable to receive the dealkylation heavy reformate, and that is operable to produce a transalkylation stage product that contains mixed xylenes; a post-dealkylation-transalkylation refining system that fluidly couples to the transalkylation stage, that is operable to receive the transalkylation stage product and that is operable to produce a benzene product, a toluene product, a mixed xylenes product and a C9+ alkyl aromatics; a recycle loop that fluidly couples the dealkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey the C9+ alkyl aromatics to the dealkylation stage; wherein the hydrodealkylation catalyst is operable to selectively convert methyl ethyl benzenes and hydrogen into toluene and the non-aromatic product gas; wherein the transalkylation catalyst is operable to selectively convert tri-methyl benzenes and toluene into mixed xylenes; wherein the hydrodealkylation catalyst and the transalkylation catalyst are not the same material, and wherein the hydrodealkylation catalyst and the transalkylation catalyst are not contained in the same stage. 13. The system of claim 12 , wherein the non-aromatic product gas separations stage and the dealkylation stage are part of the same vessel. 14. The system of claim 12 , further comprising a recycle loop that fluidly couples the dealkylation stage to the non-aromatic product gas separations stage and that is operable to convey hydrogen to the dealkylation stage. 15. The system of claim 12 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the benzene product to the transalkylation stage. 16. The system of claim 12 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the toluene product to the transalkylation stage. 17. The system of claim 12 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylation refining system and that is operable to convey at least a portion of the mixed xylene product to the transalkylation stage. 18. The system of claim 12 , where the post-dealkylation-transalkylation refining system is further operable to produce a para-xylene product, an ortho-xylene product and a meta-xylene product from the mixed xylenes. 19. The system of claim 18 , further comprising a recycle loop that fluidly couples the transalkylation stage to the post-dealkylation-transalkylat

Assignees

Inventors

Classifications

  • according to "fluidised-bed" technique (B01J8/20 takes precedence) · CPC title

  • Aromatics · CPC title

  • from hydrocarbons containing a six-membered aromatic ring, e.g. propyltoluene to vinyltoluene · CPC title

  • by exchange of hydrocarbon groups, which may be substituted, from the same of other compounds, e.g. transalkylation · CPC title

  • of types characterised by their specific structure not provided for in groups C07C2529/08 - C07C2529/65 · CPC title

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What does patent US10071939B2 cover?
The present invention relates to a method of forming mixed xylenes from a heavy reformate using a dealkylation-transalkylation system that includes the step of introducing a heavy reformate containing methyl ethyl benzenes and tri-methyl benzenes and sufficiently free of toluene into the dealkylation stage with a hydrogen-containing material such that the heavy reformate and the hydrogen-contai…
Who is the assignee on this patent?
Saudi Arabian Oil Co
What technology area does this patent fall under?
Primary CPC classification C07C4/18. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 11 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 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).