Method for producing light aromatic hydrocarbons

Patent metadata

Field	Value
Publication number	US-12516255-B2
Application number	US-202218555898-A
Country	US
Kind code	B2
Filing date	Apr 22, 2022
Priority date	Apr 23, 2021
Publication date	Jan 6, 2026
Grant date	Jan 6, 2026

Abstract

A method for producing light aromatic hydrocarbons from C 9 + aromatic hydrocarbons includes a step of contacting a C 9 + aromatic hydrocarbon with a dealkylation catalyst comprising a KL zeolite, and platinum and a modifying metal supported thereon in the presence of hydrogen, to obtain a light aromatic hydrocarbon. The modifying metal is selected from the group consisting of Group IIA metals and rare earth metals. By using a Pt/KL catalyst comprising a specific modifying metal in the dealkylation reaction of C 9 + aromatic hydrocarbons for producing light aromatic hydrocarbons, the method shows the advantages of high conversion rate of feedstock, high yield of light aromatic hydrocarbons, good reaction selectivity.

First claim

The invention claimed is:

1 . A method for producing light aromatic hydrocarbons, comprising a step of contacting a C 9 + aromatic hydrocarbon with a dealkylation catalyst in the presence of hydrogen to carry out a dealkylation reaction to obtain a light aromatic hydrocarbon, wherein the dealkylation catalyst comprises a KL zeolite, platinum, and a modifying metal supported on the KL zeolite, and the modifying metal is one or more selected from the group consisting of Group IIA metals and rare earth metals.

2 . The method according to claim 1 , wherein the dealkylation catalyst comprises the KL zeolite, 0.1-1.5% by mass of platinum, and 0.02-4.0% by mass of the modifying metal, relative to the amount of the KL zeolite.

3 . The method according to claim 1 , wherein
the rare earth metal is selected from the group consisting of La, Ce, Gd, Y, Sm, and Yb.

4 . The method according to claim 1 , wherein the dealkylation reaction is carried out at a temperature of 350-490° C., a pressure of 0.1-4.0 MPa, a mass space velocity of C 9 + aromatic hydrocarbon of 1-20 h −1 , and a molar ratio of hydrogen to C 9 + aromatic hydrocarbon of 0.5-20:1.

5 . A method for producing light aromatic hydrocarbons comprising the steps of:
1) Contacting a feedstock comprising a C 9 + paraffinic hydrocarbon with a dehydrogenation catalyst in the presence of hydrogen in a first reaction zone for a first reaction to dehydrocyclize at least a part of the C 9 + paraffinic hydrocarbon to obtain a C 9 + aromatic hydrocarbon to obtain a product stream comprising the C 9 + aromatic hydrocarbon, wherein the dehydrogenation catalyst comprises alumina and a Group VIII metal, a Group IVA metal, a Group IA metal and a halogen supported thereon; 2) Contacting the product stream comprising the C 9 + aromatic hydrocarbon obtained in step 1) with a dealkylation catalyst in the presence of hydrogen in a second reaction zone for a second reaction to dealkylate at least a part of the C 9 + aromatic hydrocarbon to obtain a light aromatic hydrocarbon, wherein the dealkylation catalyst comprises a KL zeolite, platinum, and a modifying metal supported thereon, wherein the modifying metal is selected from the group consisting of Group IIA metals and rare earth metals.

6 . The method according to claim 5 , wherein the dealkylation catalyst of step 2) comprises the KL zeolite and 0.1-1.5% by mass of platinum and 0.02-4.0% by mass of the modifying metal, relative to the amount of the KL zeolite.

7 . The method according to claim 5 , wherein the dealkylation catalyst has one or more of the following characteristics:
the Group IIA metal is selected from the group consisting of barium and calcium; the rare earth metal is selected from the group consisting of La, Ce, Gd, Y, Sm, and Yb; and/or an average diameter of grains of the KL zeolite is 0.1-2 μm.

8 . The method according to claim 5 , wherein: in step 1),
in the dehydrogenation catalyst, the Group VIII metal is selected from the group consisting of platinum, palladium, and iridium, the Group IVA metal is selected from the group consisting of tin, germanium, and silicon, the Group IA metal is selected from the group consisting of potassium, sodium, rubidium, and cesium, and the halogen is selected from the group consisting of chlorine, fluorine, bromine, and iodine; and the dehydrogenation catalyst comprises an alumina carrier and, relative to the amount of the alumina carrier, 0.1-2.0% by mass of a Group VIII metal, 0.1-2.0% by mass of a Group IVA metal, 0.01-0.2% by mass of a Group IA metal, and 0.3-5% by mass of a halogen.

9 . The method according to claim 8 , wherein the alumina carrier is γ-alumina carrier, and the dehydrogenation catalyst has a platinum content of 0.1-1.0% by mass, a tin content of 0.1-1.0% by mass, a potassium content of 0.02-0.1% by mass, and a chlorine content of 0.5-1.5% by mass, relative to the amount of the alumina carrier.

10 . The method according to claim 5 , wherein the first reaction is carried out at a reaction temperature of 400-500° C., a reaction pressure of 0.1-4.0 MPa, a mass space velocity of the feedstock comprising the C 9 + paraffinic hydrocarbon of 1-50 h −1 , and a hydrogen-to-hydrocarbon molar ratio of 0.5-20:1.

11 . The method according to claim 5 , wherein the second reaction is carried out at a temperature of 350-490° C., a pressure of 0.1-4.0 MPa, a mass space velocity of the stream comprising the C 9 + aromatic hydrocarbon of 1-20 h −1 , and a hydrogen-to-hydrocarbon molar ratio of 0.5-20:1.

12 . The method according to claim 5 , wherein the mass ratio of the dehydrogenation catalyst used in step 1) to the dealkylation catalyst used in step 2) is 1:(0.25-5).

13 . The method according to claim 5 , wherein the feedstock comprising the C 9 + paraffinic hydrocarbon is naphtha selected from the group consisting straight run naphtha, hydrocracked heavy naphtha, hydrotreated coking gasoline, raffinate of ethylene pyrolysis gasoline, catalytic cracking gasoline, and mixtures thereof.

14 . The method according to claim 13 , further comprising, prior to step 1), subjecting the naphtha to a hydrofining treatment to remove arsenic, lead, copper, sulfur and nitrogen impurities contained therein.

15 . The method according to claim 13 , wherein the first reaction is controlled such that a conversion rate of naphthenic hydrocarbon in the naphtha is not less than 90% by mass and a conversion rate of C 9 + paraffinic hydrocarbon is 70-95% by mass.

16 . The method according to claim 13 , wherein the first reaction is controlled such that a conversion rate of naphthenic hydrocarbon in the naphtha is not less than 90% by mass, wherein the conversion rates of both C 7 and C 8 naphthenic hydrocarbons in the naphtha are not less than 95% by mass, and the conversion rate of C 6 naphthenic hydrocarbon in the naphtha is not less than 70% by mass.

17 . The method according to claim 13 , wherein the first reaction is controlled such that a conversion rate of paraffinic hydrocarbon in the naphtha is not greater than 60% by mass, wherein a conversion rate of C 6 paraffinic hydrocarbon in the naphtha is not greater than 18% by mass, a conversion rate of C 7 paraffinic hydrocarbon in the naphtha is not greater than 30% by mass, a conversion rate of C 8 paraffinic hydrocarbon in the naphtha is not greater than 70% by mass, and a conversion rate of C 9 + paraffinic hydrocarbon in the naphtha is 70-95% by mass.

18 . The method according to claim 1 , wherein the dealkylation catalyst comprises the KL zeolite and 0.3-1.2% by mass of platinum and 0.1-3.0% by mass of the modifying metal, relative to the amount of the KL zeolite.

19 . The method according to claim 5 , wherein the dealkylation catalyst comprises the KL zeolite, 0.3-1.2% by mass of platinum, and 0.1-3.0% by mass of the modifying metal, relative to the amount of the KL zeolite.

20 . The method according to claim 8 , wherein the dehydrogenation catalyst comprises an alumina carrier and, relative to the amount of the alumina carrier, 0.1-1.0% by mass of a Group VIII metal, 0.1-1.0% by mass of a Group IVA metal, 0.02-0.1% by mass of a Group IA metal, and 0.5-1.5% by mass of a halogen.

21 . The method according to claim 5 , wherein the first reaction is carried out at a reaction temperature of 450-480° C., a reaction pressure of 0.1-2.0 MPa, a mass space velocity of the feedstock comprising the C 9 + paraffinic hydrocarbon of 1-10 h −1 , and a hydro

Assignees

• China Petroleum & Chem Corp
• Sinopec Res Institute Of Petroleum Processing Co Ltd

Inventors

• Liu Tong
• Wang Jieguang
• Wang Jiaxin
• Ma Aizeng
• Ren Jianqiang
• Wang Chunming
• Zhang Xinkuan
• Dong Chen

Classifications

• C10G2400/30

  Aromatics · CPC title

• C10G2300/70

  Catalyst aspects · CPC title

• B01J29/44

  Noble metals · CPC title

• B01J23/622

  with germanium, tin or lead · CPC title

• Y02P20/52

  using catalysts, e.g. selective catalysts · CPC title