Systems and methods for separation and extraction of heterocyclic compounds and polynuclear aromatic hydrocarbons from a hydrocarbon feedstock

Patent metadata

Field	Value
Publication number	US-2018187104-A1
Application number	US-201815861105-A
Country	US
Kind code	A1
Filing date	Jan 3, 2018
Priority date	Jan 4, 2017
Publication date	Jul 5, 2018
Grant date	—

Abstract

Methods of extracting 1-4 cycle heterocyclic compounds and 2-5 cycle polynuclear aromatic hydrocarbons from a hydrocarbon feedstock are described. The methods include providing a hydrocarbon feedstock containing crude oil fractions, and determining an A/R ratio and an asphaltene concentration of the hydrocarbon feedstock. Based upon the A/R ratio and the asphaltene concentration, the treatable hydrocarbon feedstock undergoes one or more of cracking and fractionating. Subsequently, at least one targeted portion of the heterocyclic compounds is extracted from the fractionated stream with an aqueous solvent. A stream containing the 2-5 cycle polynuclear aromatic hydrocarbons is transferred to an extractor and the 2-5 cycle polynuclear aromatic hydrocarbons are extracted with a solvent system comprising an aprotic solvent.

First claim

What is claimed is:

1 . A method of extracting 1-4 cycle heterocyclic compounds and 2-5 cycle polynuclear aromatic hydrocarbons from a hydrocarbon feedstock, the method comprising:
providing a hydrocarbon feedstock containing crude oil fractions comprising 1-4 cycle heterocyclic compounds and 2-5 cycle polynuclear aromatic hydrocarbons; determining an A/R ratio and an asphaltene concentration of the hydrocarbon feedstock; treating the hydrocarbon feedstock based upon the determination of the A/R ratio and asphaltene concentration to form a treatable hydrocarbon feedstock comprising fractions with a boiling point range of greater than 360° C.; cracking the treatable hydrocarbon feedstock in a cracker to form a treated hydrocarbon feedstock comprising fractions having a boiling point range of 165° C. to 470° C.; fractionating the treated hydrocarbon feedstock into a first fractionated stream having a boiling point range of less than 165° C., a second fractionated stream having a boiling point range of 165° C. to 470° C., and a third fractionated stream having a boiling point range of greater than 470° C.; extracting at least one targeted portion of the 1-4 cycle heterocyclic compounds from the second fractionated stream with an aqueous solvent comprising an ionic liquid formed from pressurized carbon dioxide and water; transferring to a PAH extractor a 1-4 cycle heterocyclic compound-lean stream containing the 2-5 cycle polynuclear aromatic hydrocarbons after all targeted portions of the 1-4 cycle heterocyclic compounds have been extracted from the second fractionated stream; and extracting the 2-5 cycle polynuclear aromatic hydrocarbons from the heteroatom-lean stream in the PAH extractor with a solvent system comprising an aprotic solvent.

2 . The method of claim 1 , in which the treated hydrocarbon feedstock comprises greater than 90% by weight fractions having a boiling point range of less than 470° C.

3 . The method of claim 1 , in which the hydrocarbon feedstock comprises at least one of heavy crude oil fractions, medium crude oil fractions, and mixtures thereof.

4 . The method of claim 1 , in which the cracking step comprises thermal cracking, steam cracking, or catalytic cracking.

5 . The method of claim 1 , in which the cracking step comprises catalytic cracking with a zeolite catalyst.

6 . The method of claim 1 , in which:
the hydrocarbon feedstock is determined to have an A/R ratio from 0.5:1 to 1.5:1 and an asphaltene concentration from 2.0 wt. % to 15 wt. %; and treating the hydrocarbon feedstock comprises:
fractionating the hydrocarbon feedstock in a vacuum fractionator to form a first hydrocarbon stream with fractions having a boiling point range of 360° C. to 470° C. and a second hydrocarbon stream with fractions having a boiling point range of greater than 470° C.;
deasphalting the second hydrocarbon stream in a solvent deasphalter to form a deasphalted oil stream and an asphalt fraction; and
hydrocracking the deasphalted oil stream in a mild hydrocracker to form the treatable hydrocarbon feedstock.

7 . The method of claim 6 , in which the hydrocracking step is conducted at a pressure from 4 MPa to 16 MPa and a temperature from 330° C. to 440° C.

8 . The method of claim 1 , in which:
the hydrocarbon feedstock is determined to have an A/R ratio from 0:1 to 0.5:1 and an asphaltene concentration from 0.0 wt. % to 2.0 wt. %; and treating the hydrocarbon feedstock comprises fractionating the hydrocarbon feedstock in a fractionator to form the treatable hydrocarbon stream having fractions with a boiling point range of greater than 360° C. and a second hydrocarbon stream having fractions with a boiling point range of less than 360° C.

9 . The method of claim 1 , in which:
the hydrocarbon feedstock is determined to have an A/R ratio from 0:1 to 0.5:1 and an asphaltene concentration from 0.0 wt. % to 2.0 wt. %; and treating the hydrocarbon feedstock comprises fractionating the hydrocarbon feedstock to form a first fractionated stream having fractions with a boiling point range of less than 360° C. and the treatable feedstock having fractions with a boiling point range of greater than or equal to 360° C.

10 . The method of claim 1 , in which extracting at least one targeted portion of the 1-4 cycle heterocyclic compounds from the second fractionated stream comprises:
extracting a first targeted portion of the 1-4 cycle heterocyclic compounds having a first polarity in a first extraction vessel operating at a first pressure; extracting a second targeted portion of the 1-4 cycle heterocyclic compounds in a second extraction vessel after extracting the first portion, the second extraction vessel operating at a second pressure greater than the first pressure, the second portion of the heteroatom compounds having a second polarity that is less than the first polarity; and extracting a third targeted portion of the 1-4 cycle heterocyclic compounds in a third extraction vessel after extracting the second portion of the 1-4 cycle heterocyclic compounds, the third extraction vessel operating at a third pressure greater than the first pressure and the second pressure, the third portion of the 1-4 cycle heterocyclic compounds having a third polarity that is less than the second polarity.

11 . The method of claim 1 , in which the extraction of each targeted portion of the 1-4 cycle heterocyclic compounds from the second fractionated stream comprises:
feeding into an extraction vessel separately or as a mixture:
the second fractionated stream; and
the aqueous solvent,
whereby the combination of the second fractionated stream with the aqueous solvent in the extraction vessel forms an extraction mixture;
tuning the aqueous solvent to selectively form solvent complexes with the targeted portion of the 1-4 cycle heterocyclic compounds in the extraction mixture, whereby the extraction mixture separates into at least a 1-4 cycle heterocyclic-compound rich phase and a 1-4 cycle heterocyclic-compound lean phase, the 1-4 cycle heterocyclic-compound rich phase containing the solvent complexes; removing the 1-4 cycle heterocyclic-compound lean phase from the extraction vessel as a 1-4 cycle heterocyclic-compound lean stream; removing the 1-4 cycle heterocyclic-compound rich phase from the extraction vessel as a 1-4 cycle heterocyclic-compound rich stream; and optionally transferring the 1-4 cycle heterocyclic-compound lean stream from the extraction vessel as a feed stream derived from the hydrocarbon feedstock to an additional extraction vessel for extraction of an additional targeted portion of heteroatom compounds from the feed stream.

12 . The method of claim 11 , in which:
tuning the aqueous solvent system comprises establishing an extraction pressure and an extraction temperature of the extraction mixture in the extraction vessel that together tune the aqueous solvent to selectively form a solvent complex with the targeted portion of the 1-4 cycle heterocyclic compounds; the extraction pressure is from 2 bar to 300 bar; and the extraction temperature of the extraction mixture is from greater than the critical temperature of carbon dioxide to 150° C.

13 . The method of claim 1 , in which extracting the 2-5 cycle polynuclear aromatic hydrocarbons comprises:
combining the 1-4 cycle heterocyclic-compound lean phase with the solvent system in the PAH extractor, whereby the 1-4 cycle heterocyclic-compound lean phase separates into a PAH-rich phase and a PAH-lean phase, the PAH-rich phase comprising a mixture of polynuclear aromatic hydrocarbons; removing the PAH-rich phase from the PAH extractor as a PAH rec

Assignees

• Saudi Arabian Oil Co

Inventors

• Yusuf Zaki
• Hammad Ahmad D
• Ballesteros Alberto Lozano

Classifications

• C10G67/049 Primary

  The hydrotreatment being a hydrocracking · CPC title

• C10G2300/1096

  Aromatics or polyaromatics · CPC title

• C10G67/0409

  Extraction of unsaturated hydrocarbons · CPC title

• C10G51/02

  plural serial stages only · CPC title

• C10G2300/1044

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