Process for removal of sulfur and other impurities from olefinic liquefied petroleum gas

Patent metadata

Field	Value
Publication number	US-11739277-B2
Application number	US-202117204732-A
Country	US
Kind code	B2
Filing date	Mar 17, 2021
Priority date	Mar 18, 2020
Publication date	Aug 29, 2023
Grant date	Aug 29, 2023

Abstract

Organic sulfur compounds which are generally present in the crude oil undergoes various transformations while processing the crude oil in the secondary processing units such as fluid catalytic cracker, hydrocracker, delayed coker, visbreaker, etc. The sulfur present in the feed which enters into these secondary processing units are distributed into various products coming out of the units. Sulfur compounds which are present in the various product fractions are removed to meet the desired specifications before routing to the final product pool. Conventionally, sulfur present in the LPG has been removed by amine treatment followed by caustic and water wash. The present invention relates to a process for removal of sulfur and other impurities from Liquefied Petroleum Gas (LPG) comprising olefins through reactive desulfurization route. The present invention is an eco-friendly process as it minimizes or eliminates the use of caustic which is conventionally used to remove the sulfur from LPG.

First claim

The invention claimed is:

1. A process for removal of sulfur and other impurities from a mixed olefinic Liquefied Petroleum Gas (LPG) stream, the process comprising:
(a) feeding the mixed olefinic LPG stream along with an oxygenate component to a reactor comprising a cation exchange resin catalyst,
wherein olefins present in the mixed olefinic LPG stream react with the sulfur present in mercaptan impurities to form alkyl sulfides and dialkyl sulfides;
wherein the olefins present in the mixed olefinic LPG stream react to form a liquid product comprising dimers, trimers, and tetramers; and
wherein the liquid product reacts with the sulfur present in mercaptan impurities and form alkyl sulfides and dialkyl sulfides;

(b) subjecting the oxygenate component, the alkyl sulfides and dialkyl sulfides along with the liquid product and a treated LPG stream to separation in a fractionating column, wherein the oxygenate component is separated and recycled back to the reactor along with a makeup oxygenate stream;
(c) sending the alkyl sulfides and alkyl disulfides along with the liquid product from the fractionating column to a hydrodesulfurization unit in a refinery, a petrochemical complex or to a fluid catalytic cracking unit; and
(d) routing the treated LPG stream from top of the fractionating column for further utilization,
wherein the sulfur content is reduced from 30-900 ppmw in the mixed olefinic LPG stream to 3-10 ppmw in the treated LPG stream.

2. The process as claimed in claim 1 , wherein the cation exchange resin catalyst is a high active cation exchange resin catalyst, a modified low active cation exchange resin catalyst or a spent catalyst.

3. The process as claimed in claim 2 , wherein the high active cation exchange resin catalyst has active site concentration in a range of 4.7-5.2 eq/kg.

4. The process as claimed in claim 2 , wherein the oxygenate component is added when the high active cation exchange resin catalyst is used.

5. The process as claimed in claim 2 , wherein the modified low active cation exchange resin catalyst is prepared by treating a fresh catalyst with a metal hydroxide solution at a rate of 10 milliliter per gram of catalyst.

6. The process as claimed in claim 5 , wherein the metal hydroxide is sodium hydroxide or potassium hydroxide.

7. The process as claimed in claim 6 , wherein concentration of the metal hydroxide is in a range of 0.1-0.5 N.

8. The process as claimed in claim 5 , wherein the modified low active cation exchange resin catalyst has active site concentration in a range of 1-3.5 eq/kg.

9. The process as claimed in claim 2 , wherein the spent catalyst has active site concentration in a range of 1-3.5 eq/kg, deposited impurities in a range of 0.5-2.5 wt. % and metals in a range of 1000-3000 ppmw.

10. The process as claimed in claim 1 , wherein the treated LPG is routed to a propylene recovery unit, a methyl tert-butyl ether unit, an ethyl tert-butyl ether unit, or a dimerization unit.

11. The process as claimed in claim 1 , wherein the oxygenate component is an alcohol.

12. The process as claimed in claim 11 , wherein the alcohol is selected from the group consisting of methanol, ethanol, and tertbutyl alcohol.

13. The process as claimed in claim 1 , wherein the oxygenate/olefin concentration is in a mole ratio of 0.03-0.15.

14. The process as claimed in claim 1 , wherein the mixed olefinic LPG stream comprises C4 olefins.

Assignees

• Indian Oil Corp Ltd

Inventors

• Subramani Saravanan
• Upadhyay Vimal Kumar
• Maji Prosenjit
• Manna Reshmi
• Sugumaran Vatsala
• VANAMAMALAI Mahalingam
• Sau Madhusudan
• Kapur Gurpreet Singh
• RAMAKUMAR Sankara Sri Venkata

Classifications

• C10L3/12 Primary

  Liquefied petroleum gas {(liquefying by pressure and cold treatment F25J)} · CPC title

• B01D3/14

  Fractional distillation {or use of a fractionation or rectification column} · CPC title

• B01J39/05

  in the strongly acidic form · CPC title

• B01J39/19

  obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds · CPC title

• C10L3/103

  Sulfur containing contaminants · CPC title