IP Library › Granted Patent US 9,856,423
Granted Patent B2
US 9,856,423 · App. 14/684,196 · Granted Jan 2, 2018

Process for deeply desulfurizing catalytic cracking gasoline

Inventors: Tianzhen Hao (Cangzhou, CN); Jinsen Gao (Beijing, CN); Dezhong Li (Cangzhou, CN); Liang Zhao (Beijing, CN); Zhiyuan Lu (Cangzhou, CN); Xingying Lan (Beijing, CN)
Assignees: Tianzhen Hao; CHINA UNIVERSITY OF PETROLEUM-BEIJING
C10G67/04C10G21/14C10G21/16C10G21/20C10G21/22C10G21/28C10G53/16C10G67/16C10G2300/202C10G2400/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,856,423
App. No.
14/684,196
Granted
Jan 2, 2018
Kind
B2
Abstract

The present invention provides a process for desulfurizing gasoline fraction by solvent extraction: introducing the gasoline fraction into an extraction tower at a lower-middle part thereof, introducing a solvent into the extraction tower at the top thereof, injecting saturated C5 hydrocarbon into a reflux device at the bottom of the extraction tower, wherein the gasoline fraction which is desulfurized flows out from the top of the extraction tower; the solvent that has extracted sulfide, aromatics and C5 hydrocarbon flows out from the bottom of the extraction tower, and is separated into a C5 hydrocarbon-containing light component, a sulfur-rich component, water and the solvent. The present invention also provides a process for deeply desulfurizing catalytic cracking gasoline, which flexibly combines the process described above and an existing desulfurization technology.

Claims (24)

1. A process for desulfurizing a catalytic cracking gasoline fraction by solvent extraction, comprising steps of:

introducing the gasoline fraction into an extraction tower at an about middle part thereof, introducing a solvent into the extraction tower at the top thereof, and injecting saturated C5 hydrocarbon into a reflux device at the bottom of the extraction tower, wherein the temperature at the top of the extraction tower is controlled between 65˜80° C., the temperature at the bottom of the extraction tower is controlled between 50˜60° C., and the pressure (absolute) at the top of the extraction tower is controlled between 0.5˜0.6 MPa, a feeding ratio by volume of the solvent to the gasoline fraction is controlled between 2.0˜3.0, and a feeding ratio by volume of the saturated C5 hydrocarbon to the gasoline fraction is controlled between 0.2˜0.3, and wherein the gasoline fraction and the solvent are contacted at an upper section of the extraction tower via a multi-stage countercurrent, meanwhile the saturated C5 hydrocarbon and the solvent are contacted at a lower section of the extraction tower, the gasoline fraction which is desulfurized by extraction flows out from the top of the extraction tower, as a material A, and the solvent that has extracted sulfide, aromatics and the C5 hydrocarbon flows out from the bottom of the extraction tower, as a material B; washing the material A for removing solvent therein, to obtain a desulfurized gasoline fraction; further treating the material B to separate a C5 hydrocarbon-containing light component, a sulfur-rich component, water and the solvent, wherein the C5 hydrocarbon-containing light component contains the saturated C5 hydrocarbon and a C5 olefin, wherein the further treating the material B specifically comprises steps of:

{circle around (1)} introducing the material B into an extraction distillation tower at the top thereof, wherein the pressure (absolute) of the extraction distillation tower is controlled between 0.15˜0.3 MPa, and the temperature at the bottom of the extraction distillation tower is controlled between 150˜180° C., the C5 hydrocarbon-containing light component is distilled out as material C from the top of the extraction distillation tower, and a sulfur-rich solvent is obtained as material D at the bottom of the extraction distillation tower;

{circle around (2)} after being condensed, returning the material C obtained in step {circle around (1)} to the reflux device at the bottom of the extraction tower; introducing the material D into a recycling tower from a middle part thereof, wherein the pressure (absolute) of the recycling tower is controlled between 0.015˜0.05 MPa, and the temperature at the bottom of the recycling tower is controlled between 130˜180° C.; a material E, i.e, a sulfur-rich oil containing sulfide, aromatics and cycloolefin, is obtained at the top of the recycling tower; a material F that mainly contains solvent is obtained at the bottom of the recycling tower; and

{circle around (3)} after being condensed, conducting a water oil separation on the material E obtained in step {circle around (2)}, to obtain water and a sulfur-rich component G; returning a portion of the water to the top of the recycling tower in step {circle around (2)}, and returning the rest as washing water to the step of washing the material A for removing solvent; returning the material F obtained in step {circle around (2)}, after heat-exchange, to the top of the extraction tower for recycling;

wherein the solvent is a mixed solvent containing one or two of diethylene glycol, triethylene glycol, tetraethylene glycol, dimethyl sulfoxide, sulfolane, N-formyl morpholine, N-methyl pyrrolidone, polyethylene glycol, and propylene carbonate; and the water content of the solvent is 0.6˜0.8% by weight.

2. The process for desulfurizing a gasoline fraction by solvent extraction according to claim 1 , wherein the gasoline fraction is a light gasoline fraction with a boiling point of less than 130° C.

3. The process for desulfurizing a gasoline fraction by solvent extraction according to claim 1 , wherein the water for washing the material A accounts for 1.0˜10.0% by weight of the material A.

4. The process for desulfurizing a gasoline fraction by solvent extraction according to claim 1 , wherein: in step {circle around (1)}, the pressure of the extraction distillation tower is controlled at 0.2 MPa, and the temperature at the bottom of the extraction distillation tower is controlled at 160° C.; in step {circle around (2)}, the pressure of the recycling tower is controlled between 0.035˜0.045 MPa, and the temperature at the bottom of the recycling tower is controlled between 165˜175° C.

5. A process for deeply desulfurizing catalytic cracking gasoline, comprising steps of:

1) separating the catalytic cracking gasoline into a light gasoline fraction, a medium gasoline fraction and a heavy gasoline fraction, wherein the cutting point between the light gasoline fraction and the medium gasoline fraction is 35˜50° C., the cutting point between the medium gasoline fraction and the heavy gasoline fractions 70˜130° C.;

2) conducting a mercaptan removal treatment on the light gasoline fraction obtained in step 1), to obtain a desulfurized light fraction having a sulfur content of less than 10 ppm and a sulfur-rich component H;

3) treating the medium gasoline fraction obtained in step 1) according to the process for desulfurizing a gasoline fraction by solvent extraction as claimed in claim 1 , to obtain a desulfurized medium fraction having a sulfur content of less than 10 ppm and a sulfur-rich component G; and

4) conducting a desulfurization treatment on the heavy gasoline fraction obtained in step 1), together with the sulfur-rich component H obtained in step 2) and the sulfur-rich component G obtained in step 3) by using a selective hydrodesulfurization process, to obtain a desulfurized heavy fraction having a sulfur content of less than 10 ppm.

6. The process for deeply desulfurizing catalytic cracking gasoline according to claim 5 , wherein: before separating catalytic cracking gasoline in step 1), micromolecular mercaptan in the catalytic cracking gasoline is converted into macromolecular sulfide with a high boiling point via an alkali-free sweetening or prehydrogenation process.

7. The process for deeply desulfurizing catalytic cracking gasoline according to claim 5 , wherein: the light gasoline fraction obtained in step 2) is introduced into the reflux device of the extraction tower used in the extraction desulfurization process in step 3).

8. A process for deeply desulfurizing catalytic cracking gasoline, comprising steps of:

i) separating the catalytic cracking gasoline into a light gasoline fraction I and a heavy gasoline fraction I at a cutting point of 50˜130° C.;

ii) treating the light gasoline fraction I obtained in step i) according to the process for desulfurizing a gasoline fraction by solvent extraction in claim 1 , to obtain a desulfurized light fraction I having a sulfur content of less than 10 ppm and a sulfur-rich component J; and

iii) conducting a desulfurization treatment on the heavy gasoline fraction I obtained in step i) together with the sulfur-rich component J obtained in step ii) by using a selective hydrodesulfurization process, to obtain a desulfurized heavy fraction I having a sulfur content of less than 10 ppm.

9. The process for deeply desulfurizing catalytic cracking gasoline according to claim 8 , wherein: in step ii), the light gasoline fraction I obtained in step i) is subjected to a mercaptan removal treatment firstly, and then the resulting mercaptan-removed light gasoline fraction I′ is finely cut into a light gasoline fraction II and a medium gasoline fraction I at a cutting point of 35˜50° C., and then the medium gasoline fraction I is subjected to the desulfurizing treatment according to the process for desulfurizing a gasoline fraction by solvent extraction in claim 1 to obtain a desulfurized medium fraction I having a sulfur content of less than 10 ppm and a sulfur-rich component K; and the sulfur-rich component K instead of the sulfur-rich component J is introduced into the step iii) to be desulfurized together with the heavy gasoline fraction.

10. The process for deeply desulfurizing catalytic cracking gasoline according to claim 8 , wherein: in step ii), the light gasoline fraction I obtained in step i) is subjected to a mercaptan removal treatment by extraction firstly to obtain a mercaptan-removed light gasoline fraction I′ and a sulfur-rich component L, and then the mercaptan-removed light gasoline fraction I′ is subjected to the desulfurizing treatment according to the process for desulfurizing a gasoline fraction by solvent extraction in claim 1 to obtain a desulfurized light fraction II having a sulfur content of less than 10 ppm and a sulfur-rich component M; and the sulfur-rich component L and the sulfur-rich component M instead of the sulfur-rich component J are introduced into the step iii) to be desulfurized together with the heavy gasoline fraction.

11. The process for desulfurizing a gasoline fraction by solvent extraction according to claim 1 , wherein the gasoline fraction is a light gasoline fraction with a boiling range of 40˜100° C.

12. The process for desulfurizing a gasoline fraction by solvent extraction according to claim 1 , wherein the water for washing the material A accounts for 2˜4% by weight of the material A.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2020
From: HAO, TIANZHEN; CHINA UNIVERSITY OF PETROLEUM-BEIJING
To: HEBEI REFINING TECHNOLOGIES COMPANY LIMITED; CHINA UNIVERSITY OF PETROLEUM-BEIJING
Reel/Frame 053221/0829 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2015
From: HAO, TIANZHEN; GAO, JINSEN; LI, DEZHONG; ZHAO, LIANG; LU, ZHIYUAN; LAN, XINGYING
To: HAO, TIANZHEN; CHINA UNIVERSITY OF PETROLEUM-BEIJING
Reel/Frame 035412/0733 →
Priority Claims (1)
CN 2013 1 0581366 · Nov 18, 2013 · national
Continuity (2)
Continuation PCTCN2014070817 · Jan 17, 2014
Related Publication 20150210941A1 · Jul 30, 2015