Process for preparing linear alkyl benzene

Patent metadata

Field	Value
Publication number	US-11370723-B2
Application number	US-201917312307-A
Country	US
Kind code	B2
Filing date	Dec 9, 2019
Priority date	Dec 9, 2018
Publication date	Jun 28, 2022
Grant date	Jun 28, 2022

Abstract

The present disclosure relates to a process for preparing linear alkyl benzne (LAB). The process comprises alkylation of benzene with an alkylating agent in the presence of an ionic liquid to obtain a first product mixture comprising a first organic phase and a first aqueous phase comprising first partially spent ionic liquid. The first organic phase is deacidified and fractionally distilled to obtain a fraction comprising LAB and a fraction comprising HAB. The fraction comprising HAB is transalkylated with benzene in the presence of the ionic liquid to obtain a second product mixture comprising a second organic phase comprising LAB and a second aqueous phase comprising second partially spent ionic liquid. The partially spent ionic liquids are regenerated, and reused in the steps of alkylation or transalkylation for at least 6 cycles.

First claim

The invention claimed is:

1. A process for preparing linear alkyl benzene by alkylation of benzene, said process comprising the following steps:
a) alkylating benzene with an alkylating agent in the presence of an ionic liquid to obtain a first product mixture;
b) allowing the first product mixture to settle to obtain a first biphasic mixture comprising a first organic phase and a first aqueous phase, wherein the first organic phase comprises linear alkyl benzene (LAB), heavier alkyl benzene (HAB) and unreacted benzene, and the first aqueous phase comprises first partially spent ionic liquid;
c) deacidifying the first organic phase to obtain a deacidified first organic phase;
d) fractionally distilling the deacidified first organic phase to obtain a fraction comprising unreacted benzene, a fraction comprising LAB and a fraction comprising HAB;
e) transalkylating the fraction comprising HAB with benzene in the presence of the ionic liquid at a temperature in the range of 70° C. to 120° C. to obtain a second product mixture;
f) allowing the second product mixture to settle to obtain a second biphasic mixture comprising a second organic phase and a second aqueous phase; wherein the second organic phase comprises LAB and the second aqueous phase comprises second partially spent ionic liquid;
g) deacidifying the second organic phase, and fractionally distilling the deacidified second organic phase to obtain a fraction comprising LAB and a fraction comprising unreacted HAB; and
h) regenerating the first partially spent ionic liquid obtained in step (b) and/or and the second partially spent ionic liquid obtained in step (f), and reusing the regenerated ionic liquid in the steps of alkylating and/or transalkylating for at least 6 cycles of regeneration;
wherein the ionic liquid used in alkylation step and transalkylation step is at least one selected from the group consisting of fresh ionic liquid, regenerated ionic liquid, the first partially spent ionic liquid and the second partially spent ionic liquid;
wherein the step (h) of regeneration of partially spent ionic liquid involves the following sub-steps:
i. mixing the first partially spent ionic liquid obtained in step (b) and/or the second partially spent ionic liquid obtained in step (f) with a fourth fluid medium and an alkali followed by stirring the resultant mixture to obtain a suspension comprising a solid phase and a liquid phase;
ii. separating the solid phase from the suspension; and
iii. mixing the separated solid phase with a metal halide to obtain regenerated ionic liquid;

wherein the alkali is at least on selected from the group consisting of triethylamine, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, sodium hydroxide, and potassium hydroxide;
wherein the separated solid is at least one basic component of ionic liquid selected from the group consisting of NR 1 R 2 R 3 , (NR 1 R 2 R 3 ) i , M1Xj , M1OH, and BMIMX i ; and the fourth fluid medium is at least one selected from the group consisting of ethyl acetate, water, and methyl acetate.

2. The process as claimed in claim 1 , wherein the alkylating agent is at least one olefin selected from the group consisting of C10 to C14 olefins.

3. The process as claimed in claim 1 , wherein the alkylating agent is a hydrocarbon mixture comprising paraffins and olefins, and the volume ratio of paraffins to olefins in the hydrocarbon mixture is in the range of 20:1 to 4:1.

4. The process as claimed in claim 1 , wherein the mole ratio of benzene to the alkylating agent is in the range of 3:1 to 20:1.

5. The process as claimed in claim 1 , wherein the alkylation step (a) is carried out in two stages, wherein the first stage comprises alkylating benzene with a first portion of the alkylating agent to obtain a first resultant mixture comprising unreacted benzene, and the second stage comprises alkylating the first resultant mixture comprising unreacted benzene with a second portion of the alkylating agent to obtain the first product mixture.

6. The process as claimed in claim 1 , wherein the alkylation step is carried out at a temperature in the range of 5° C. to 150° C.

7. The process as claimed in claim 1 , wherein the alkylation step is carried out at a pressure in the range of 1 atmosphere to 50 atmosphere.

8. The process as claimed in claim 1 , wherein the volume ratio of the ionic liquid to benzene is in the range of 1:1000 to 1:10.

9. The process as claimed in claim 1 , wherein the ionic liquid is a metal halide based ionic liquid obtained by mixing an acidic component with a basic component, wherein the acidic component is a metal halide and the basic component is at least one selected from the group consisting of (NR 1 R 2 R 3 ) i M 1 X j , M 1 (OH) m , M i X j , and BMIMX i ,
wherein M 1 and M i are metals independently selected from the group consisting of Al, Fe, Zn, Cu, Ni, Ga, Ge and In;
‘BMIM’ represents 1-Butyl-3-methylimidazolium; and
Xj and X i are halogens independently selected from the group consisting of fluorine, chlorine, bromine and iodine.

10. The process as claimed in claim 1 , wherein the ionic liquid is represented by formula (I).
[(NR 1 R 2 R 3 ) i M 1 ] n+ [(M 2 Y k ) L X j ] n−   Formula (I)

wherein, NR 1 R 2 R 3 represents an amine, wherein R 1 , R 2 and R 3 are independently selected from the group consisting of alkyl, aryl and H;
M 1 and M 2 are metals independently selected from the group consisting of Al, Fe, Zn, Cu, Ni, Ga, Ge and In;
X and Y are halogens independently selected from the group consisting of fluorine, chlorine, bromine and iodine;
‘n’ represents 1 to 4, T represents 1 to 6, T represents 1 to 4, ‘k’ represents 1 to 4, represents 1 to 7, M 1 =M 2 or M 1 ≠M 2 , and X═Y or X≠Y,
wherein the ionic liquid represented by Formula I is prepared by mixing a metal halide of formula M 2 Y k with a basic component of the formula (NR 1 R 2 R 3 ) i , M 1 X j .

11. The process as claimed in claim 1 , wherein the ionic liquid is represented by formula (III),
[UM i X j ]S   Formula (III)

wherein, ‘U’ represents urea; M i X j represents metal halide, wherein M is at least one metal selected from the group consisting of Al, Fe, Zn, Ge, Cu, Ni, In, and Ga; and X is at least one halogen selected from the group consisting of fluorine, chlorine, bromine and iodine;
‘i’ represents 1 to 6, ‘j’ represents 1 to 6;
‘S’ represents a second fluid medium selected from the group consisting of benzene, and toluene;
wherein the weight % of the second fluid medium in the ionic liquid of formula III is in the range of 10 to 60%; and
wherein the ionic liquid represented by Formula III is prepared by mixing a metal halide of formula M i X j with urea as a basic component.

12. The process as claimed in claim 1 , wherein the ionic liquid is represented by formula (IV),
[BMIM][MX i Y j ) k ]  Formula (IV)

wherein, ‘BMIM’ represents 1-Butyl-3-methylimidazolium, M is at least one metal selected from the group consisting of Al, Fe, Ni, Cu, Zn, Ga, Ge, and In;
X and Y are halogens independently selected from the group consisting of chloride, bromide, fluoride and iodide;
‘i’ represents 1 to 4, ‘j’ represents 1 to 4, X═Y or X≠Y;
the ionic liquid of formula IV is optionally mixed with a third fluid medium selected from the group consisting of benzene, and toluene, wherein the weight % of the third fluid medium and the ionic liquid of formula IV is in the range of 10% to 40%; and
wherein the ionic liquid represented by Formula IV is prepared by mixing the metal halide of formula MY j with the basic component of the formula BMIMX i .

13. The process as claimed i

Assignees

• Reliance Industries Ltd

Inventors

• Kotra Viswanath
• Aduri Pavankumar
• Dhukande Vibhuti
• Sakhalkar Mangesh Raghunath
• Ratnaparkhi Uday Meghashyam
• Kumbhar Rahul
• Iyengar Suresh
• Dhawade Rahul Mahadeo
• Chafle Romal
• Uppara Parasuveera
• Goyal Gordhan Das

Classifications

• C07C7/04

  by distillation · CPC title

• C07C2/66 Primary

  Catalytic processes · CPC title

• C07C2531/18

  containing nitrogen, phosphorus, arsenic or antimony · CPC title

• C07C6/12

  of exclusively hydrocarbons containing a six-membered aromatic ring · CPC title

• C10G29/205 Primary

  by reaction with hydrocarbons added to the hydrocarbon oil · CPC title