IP Library Granted Patent US 11,066,343
Granted Patent B2
US 11,066,343 · App. 16/349,394 · Granted Jul 20, 2021

Method for producing p-xylene

Inventors: Yasuhiro Araki (Tokyo, JP); Mayumi Yokoi (Tokyo, JP); Ryoji Ida (Tokyo, JP); Atsushi Segawa (Tokyo, JP); Masanari Akiyama (Tokyo, JP)
Assignee: ENEOS CORPORATION
C07C2/24B01J21/04B01J23/005B01J23/02B01J23/26B01J23/62B01J23/626C07C2/28C07C5/2506C07C5/333C07C5/415C07C5/417C07B61/00C07C2521/04C07C2521/10C07C2521/12C07C2523/26C07C2523/42C07C2523/62Y02P20/52
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Quick Facts
Patent No.
US 11,066,343
App. No.
16/349,394
Granted
Jul 20, 2021
Kind
B2
Abstract

Provided is a method for producing p-xylene, comprising: a provision step of providing a C4 fraction comprising at least isobutene as a product formed by fluidized catalytic cracking of a heavy oil fraction; a dimerization step of bringing a first raw material comprising the isobutene into contact with a dimerization catalyst to produce a C8 component comprising a dimer of isobutene; and a cyclization step of bringing a second raw material comprising the C8 component with a dehydrogenation catalyst to produce p-xylene through a cyclization/dehydrogenation reaction of the C8 component.

Claims (27)

1. A method for producing p-xylene, comprising:

providing a C4 fraction comprising at least isobutene as a product formed by fluidized catalytic cracking of a heavy oil fraction;

bringing a first raw material comprising the isobutene into contact with a dimerization catalyst to produce a C8 component comprising a dimer of the isobutene; and

bringing a second raw material comprising the C8 component into contact with a dehydrogenation catalyst to produce p-xylene through a cyclization/dehydrogenation reaction of the C8 component, wherein

the dehydrogenation catalyst comprises supported metals comprising

at least one metal element in group 14 and

Pt

supported on a support comprising

Al and

at least one metal element in group 2, and

the molar ratio of the at least one metal element in group 14 to Pt (number of moles of at least one metal element in group 14/number of moles of Pt) in the dehydrogenation catalyst is from 5.4 to 15, and

the content of the at least one metal element in group 14 in the dehydrogenation catalyst is 4 mass % or more based on the total mass of the dehydrogenation catalyst.

2. The method according to claim 1 , wherein the C4 fraction further comprises isobutane, normal butene and normal butane.

3. The method according to claim 2 , further comprising

obtaining a fraction (A) comprising the isobutene and the isobutane and a fraction (B) comprising the normal butene and the normal butane from the C4 fraction.

4. The method according to claim 3 , wherein the first raw material comprises the fraction (A).

5. The method according to claim 3 , further comprising

obtaining a fraction comprising isobutene (A-1) and a fraction comprising isobutane (A-2) from the fraction (A).

6. The method according to claim 5 , wherein the first raw material comprises the fraction (A-1).

7. The method according to claim 3 , further comprising

bringing a third raw material comprising the fraction (B) into contact with a dehydrogenation catalyst to produce butadiene.

8. The method according to claim 3 , further comprising

bringing a third raw material comprising the fraction (B) into contact with an isomerization catalyst to produce isobutene and isobutane.

9. The method according to claim 8 , wherein the produced isobutene is used as a part of the first raw material.

10. The method according to claim 1 , wherein the dimerization catalyst comprises at least one acidic catalyst selected from the group consisting of sulfuric acid, zeolite, solid phosphoric acid, hydrofluoric acid, an ionic liquid, and an ion exchange resin.

11. The method according to claim 1 , wherein the dehydrogenation catalyst comprises an inorganic oxide support comprising Al and Mg, and an active metal supported on the inorganic oxide support.

12. The method according to claim 11 , wherein the active metal comprises Pt and Sn.

Assignments (2)
CHANGE OF NAME Recorded Mar 9, 2021
From: JXTG NIPPON OIL & ENERGY CORPORATION
To: ENEOS CORPORATION
Reel/Frame 055538/0207 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2019
From: ARAKI, YASUHIRO; YOKOI, MAYUMI; IDA, RYOJI; SEGAWA, ATSUSHI; AKIYAMA, MASANARI
To: JXTG NIPPON OIL & ENERGY CORPORATION
Reel/Frame 049159/0405 →
Priority Claims (1)
JP JP2016-223197 · Nov 16, 2016 · national
Continuity (1)
Related Publication 20190263731A1 · Aug 29, 2019