Multi-stage fractionation of FCC naphtha with post treatment and recovery of aromatics and gasoline fractions

Patent metadata

Field	Value
Publication number	US-10774276-B2
Application number	US-201816155267-A
Country	US
Kind code	B2
Filing date	Oct 9, 2018
Priority date	Oct 9, 2018
Publication date	Sep 15, 2020
Grant date	Sep 15, 2020

Abstract

A stream of cracked naphtha is fractionated into at least four specified fractions defined by their respective boiling point ranges. The lightest fraction, IBP to 50° C., is treated in a selective etherification or alkylation process to reduce its RVP value and increase its RON. The second fraction, 50° C. to 150° C., is selectively hydrogenated to treat and convert the diolefins present and the treated stream is sent directly to the gasoline blending pool since it has the desired RON and low sulfur content. The third, and optionally a fourth fraction, boiling in the range of 50° C. to 180° C., in an embodiment, are utilized for the production of aromatics and the raffinate stream, after aromatic extraction, is sent to the gasoline blending pool. A fraction of this latter stream can optionally be recycled for further cracking to produce additional aromatics and gasoline blending components. The heaviest fraction, 180° C. to MBP, constitutes a relatively small volume and is hydrotreated at high pressure, and one portion of the hydrotreated stream is recycled to the FCC unit for further processing and the remaining hydrotreated portion is sent to the gasoline blending pool.

First claim

The invention claimed is:

1. A process for treating a feedstream of cracked naphtha to produce aromatics and gasoline blending components, the process comprising:
a. introducing the feedstream into a fractionating column and fractionating the cracked naphtha into five fractions based on boiling point ranges in which
i. a first fraction has a boiling point ranging from the initial boiling point (IBP) of the feed up to 50° C., contains no or substantially no aromatics and comprises a substantial proportion of the olefins present in the original cracked naphtha feed,
ii. a second fraction has an initial boiling point that is the final boiling point of the first fraction and a final boiling point of 100° C.,
iii. a third fraction has an initial boiling point that is the final boiling point of the second fraction and a final boiling point of 150° C.,
iv. a fourth fraction has an initial boiling point that is the final boiling point of the third fraction and a final boiling point of 180° C., and
v. a fifth fraction has an initial boiling point that is the final boiling point of the fourth fraction and a final boiling point that is the maximum boiling point (MBP) of the cracked naphtha feed entering the fractionation column;

b. passing the first fraction for processing to reduce the RVP value by subjecting the fraction to a selective etherification or alkylation process and directing the treated stream to a gasoline blending pool;
c. passing the second fraction to a selective hydrogenation processing zone to catalytically convert diolefins to mono-olefins and light sulfur components into heavier sulfur-containing components;
d. passing the selectively hydrogenated product stream of step (c) to the gasoline blending pool;
e. optionally passing the third fraction to a selective hydrogenation unit to catalytically convert diolefins to mono-olefins and passing the selectively hydrogenerated stream or the untreated third fraction to an aromatics extraction unit;
f. passing the fourth fraction to a hydrotreating unit and passing the hydrotreated stream and the third fraction to the aromatics extraction unit;
g. recovering from the aromatic extraction unit an aromatic rich stream, which is directed for further aromatic processing, and an aromatic-lean stream composed mainly of paraffins, isoparaffins, and olefins, and passing the aromatic-lean stream to a hydrotreating unit, and passing the hydrotreated stream to the gasoline blending pool; and
h. passing the fifth fraction to a hydroconverting unit and passing all or a predetermined portion of the hydroconverted product stream to an FCC unit as a recycle stream and passing any remaining portion to the gasoline blending pool.

2. The process of claim 1 , wherein the boiling cut point of the second fraction is 75° C., whereby the boiling range of the second fraction is from 50° to 75° C. and the boiling range of the third fraction is from 75° to 150° C.

3. The process of claim 1 , wherein the third fraction is passed to a common hydrotreating unit with the fourth fraction without further hydrotreating downstream of the aromatic extraction unit.

4. The process of claim 1 , wherein the third fraction is sent directly to the aromatic extraction unit.

5. The process of claim 1 , wherein the final boiling point of the first fraction is 50° C.

6. The process of claim 1 , wherein the selectively hydrogenated stream is hydrotreated to reduce its sulfur content.

7. The process of claim 1 , wherein the third fraction is sent to a common hydrotreating unit with the fourth fraction prior to the aromatics extraction unit.

8. The process of claim 1 , wherein all of the fifth fraction is recycled to FCC unit after the hydroconverting unit.

9. The process of claim 1 , wherein all of the fifth fraction is sent to the gasoline pool after the hydroconverting unit.

10. The process of claim 1 , wherein the third fraction is passed to a separate hydrotreating unit before it is mixed with the hydrotreated fourth fraction upstream of the aromatics extraction unit.

11. A process for treating a feedstream of cracked naphtha to produce aromatics and gasoline blending components comprising:
a. fractionating the cracked naphtha into four fractions based on boiling point in which:
i. the first fraction having a boiling point below 50° C. that contains no or substantially no aromatics and a substantial proportion of olefins present in the original cracked naphtha feed,
ii. a second fraction having an initial boiling point that is the final boiling point of the first fraction and a final boiling point of 150° C. that contains a substantial proportion of the aromatics and olefins present in the original feed,
iii. a third fraction having an initial boiling point that is the final boiling point of the second fraction and a final boiling point of 180° C., and
iv. a fourth fraction with an initial boiling point that is of the final boiling point of the third fraction and a final boiling point that is the maximum boiling point (MBP) of the feed entering the fractionation column;

b. optionally passing the first fraction for processing to reduce the Reid vapor pressure (RVP) value and increase the research octane number (RON) by subjecting the fraction to a selective etherification or alkylation process and directing the treated stream or untreated first fraction to a gasoline blending pool;
c. passing the second fraction to a selective hydrogenation process to catalytically convert the corresponding diolefins to mono-olefins;
d. passing the selectively hydrogenated product to a splitter operating under predetermined conditions to divide the product into two streams based on boiling point, and recovering from the splitter a first light stream having a boiling not exceeding 100° C. and a second heavy stream boiling up to the final boiling point of the selectively hydrogenated product, wherein the first light stream is sent directly to the gasoline blending pool without further hydrotreatment, and the second heavy stream is sent to an aromatic extraction unit;
e. passing the third fraction to a hydrotreating unit, recovering and combining the hydrotreated third fraction with the second heavy stream from the splitter prior to passing the combined streams to the aromatic extraction unit;
f. recovering from the aromatic extraction unit an aromatic-lean stream comprising as a major proportion paraffins, isoparaffins and olefins, the aromatic-lean stream being passed to a hydrotreating unit, and passing the hydrotreated stream to the gasoline blending pool, where the hydrotreating unit care be placed upstream or downstream of the aromatic extraction unit; and
g. passing the fourth fraction to a hydroconverting unit and passing all or a portion of the hydroconverted stream to either an FCC unit as a recycle stream or to the gasoline blending pool.

12. The process of claim 11 , wherein the Reid vapor pressure value of the first fraction is decreased by passing the first fraction for treatment to an alkylation unit or a selective etherification unit.

13. The process of claims 11 or 12 , wherein the first fraction is subjected to a selective etherification process.

14. The process of claim 13 , wherein the selective etherification process employs an alcohol under acidic conditions and reaction temperatures ranging from 20° to 80° C.

15. The process of claim 14 , wherein the alcohol is methanol.

16. The process of claim 11 , wherein the splitter in step 11(d) separates the selectively hydrogenated stream into a light stream boiling in the range of 50°-75° C. and a heavy stream boiling in t

Assignees

• Saudi Arabian Oil Co

Inventors

• Alshareef Ali H

Classifications

• C10G7/00 Primary

  Distillation of hydrocarbon oils · CPC title

• C10G45/02

  to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing · CPC title

• C10G2300/1044

  Heavy gasoline or naphtha having a boiling range of about 100 - 180 °C · CPC title

• C10G67/04

  including solvent extraction as the refining step in the absence of hydrogen · CPC title

• C10G69/04 Primary

  including at least one step of catalytic cracking in the absence of hydrogen · CPC title