METHOD FOR EFFICIENT USE OF HYDROGEN IN AROMATICS PRODUCTION FROM HEAVY AROMATICS

• US 20100160699A1
• Filed: 12/23/2008
• Published: 06/24/2010
• Est. Priority Date: 12/23/2008
• Status: Abandoned Application

• Current Assignee: UOP Llc (Honeywell International Inc.)
• Original Assignee: UOP Llc (Honeywell International Inc.)
• Inventors: FREY, Stanley Joseph, Thakkar, Vasant P.
• Application Number:
  US12/342,867
• Publication Number:
  US 20100160699A1
• Time in Patent Office: Days
• US Class Current: 585/316
• CPC Class Codes: C07C 15/04 Benzene
• CPC Class Codes: C07C 15/06 Toluene
• CPC Class Codes: C07C 15/08 Xylenes
• CPC Class Codes: C10G 2300/1044 Heavy gasoline or naphtha having a boiling range of about 100 - 180 °C
• CPC Class Codes: C10G 2300/1096 Aromatics or polyaromatics
• CPC Class Codes: C10G 2300/301 Boiling range
• CPC Class Codes: C10G 2400/04 Diesel oil
• CPC Class Codes: C10G 2400/30 Aromatics
• CPC Class Codes: C10G 65/12 including cracking steps and other hydrotreatment steps
• CPC Class Codes: C10G 67/02 plural serial stages only

Abstract

A method for efficient use of hydrogen in aromatics production from heavy aromatic oil. A hydrocarbonaceous stream comprising C₉⁺ hydrocarbons and an essentially pure hydrogen stream are hydrotreated and hydrocracked to produce a hydrocracking zone effluent comprising aromatics. The hydrocracking zone effluent is fractionated to separately recover C₄ and lighter hydrocarbons, hydrocarbons boiling between about 180° F. and about 380° F., and diesel. The heavier hydrocarbons are combined with a low purity hydrogen-containing stream and heated, then dehydrogenated or transalkylated to form hydrogen, volatile compounds, and aromatics. The hydrogen and volatile components are separated from the aromatics and treated by pressure swing adsorption to provide an essentially pure hydrogen-containing stream, which is compressed and provided to the hydrotreating and hydrocracking steps. Liquid products are recovered from the aromatics-containing stream.

Claims

1. A method for integrating the hydrogen flow in a product-producing reaction system having at least one first reaction unit that consumes a large quantity of hydrogen at high purity and at least one second reaction unit that does not consume a large quantity of hydrogen, but which requires the presence of hydrogen and can tolerate the presence of hydrogen at low purity, said method comprising:

(a) reacting a first reactant and an essentially pure hydrogen stream in the at least one first reaction unit to produce a first effluent stream;

(b) fractionating the first effluent stream to recover at least one first product stream;

(c) introducing a low-purity hydrogen-containing stream to the at least one first product stream from step (b) to form a combined stream;

(d) reacting the combined stream to form a second product stream comprising hydrogen, volatile compounds, and a product;

(e) separating the hydrogen and volatile components from the product to form a gaseous stream and a product-containing stream;

(f) purifying the gaseous stream to provide an essentially pure hydrogen-containing stream;

(g) increasing the pressure on the essentially pure hydrogen-containing stream and introducing it to the at least one first reaction unit of step (a); and

(h) recovering the product.

4. The method of claim 1, wherein the conversion in step (d) is enhanced by the inclusion of contaminants in the low-purity hydrogen-containing stream.

2. A method for balancing hydrogen needs in a petroleum refinery, said method comprising

feeding an impure hydrogen stream to an aromatics zone,

reacting the impure hydrogen stream with other hydrocarbons in the aromatics zone to produce an effluent,

separating a hydrogen-rich stream from the effluent,

purifying the hydrogen-rich stream to yield an essentially pure hydrogen stream, and

compressing the essentially pure hydrogen stream and feeding the essentially pure hydrogen stream to high-pressure hydrotreating and hydrocracking reactors.

3. The method of claim 2, wherein the aromatics zone comprises at least a dehydrogenation reactor and the other hydrocarbons comprise a light naphtha stream.

5. A method for efficiently using hydrogen in aromatics production from heavy aromatic oil, said method comprising:

(a) contacting a hydrocarbonaceous stream comprising C₉⁺ hydrocarbons and an essentially pure hydrogen stream serially with a hydrotreating catalyst under hydrotreating conditions and a hydrocracking catalyst under hydrocracking conditions in a hydrocracking zone and, respectively, to produce a hydrocracking zone effluent comprising xylenes;

(b) fractionating the hydrocracking zone effluent in a fractionation zone to separately recover a first stream of hydrocarbons comprising C₄ and lighter hydrocarbons, a second stream of hydrocarbons comprising hydrocarbons boiling below about 195°

F., a third stream comprising hydrocarbons boiling between about 180°

F. and about 380°

F., and a fourth stream comprising diesel;

(c) introducing a low purity hydrogen-containing stream to the third stream from step (b) to form a combined stream and heating the combined stream to form a heated combination;

(d) contacting the heated combination with a dehydrogenation catalyst to form a dehydrogenated stream;

(e) separating the hydrogen and volatile components from the aromatics to form a gaseous stream and an aromatic-containing stream;

(f) subjecting the gaseous stream to pressure swing adsorption to provide an essentially pure hydrogen-containing stream;

(g) increasing the pressure on the essentially pure hydrogen-containing stream and introducing it to the hydrocracking zone of step (a); and

(h) recovering the liquid hydrocarbon products in the aromatic-containing stream.

6. The method of claim 5, further comprising contacting the dehydrogenated stream of step (d) with transalkylation catalyst to form an effluent comprising hydrogen, volatile compounds, and aromatics.

7. The method of claim 5, further comprising fractionating the aromatics-containing stream of step (h) to form a benzene fraction, a toluene fraction, and a xylenes fraction.

8. The method of claim 6, further comprising fractionating the aromatics-containing stream of step (h) to form a benzene fraction, a toluene fraction, and a xylenes fraction.

9. The method of claim 6, further comprising recycling the toluene fraction to the transalkylation reactor.

10. The method of claim 8, further comprising recycling the toluene fraction to the transalkylation reactor.

11. The method of claim 7, further comprising fractionating the xylenes fraction to form a stream containing C₉-C₁₀ alkylaromatic compounds, mixing that stream with the dehydrogenated stream of step (d), and contacting the mixture with the transalkylation catalyst.

12. The method of claim 8, further comprising fractionating the xylenes fraction to form a stream containing C₉-C₁₀ alkylaromatic compounds, mixing that stream with the dehydrogenated stream of step (d), and contacting the mixture with the transalkylation catalyst.

13. The method of claim 9, further comprising fractionating the xylenes fraction to form a stream containing C₉-C₁₀ alkylaromatic compounds, mixing that stream with the dehydrogenated stream of step (d), and contacting the mixture with the transalkylation catalyst.

14. The method of claim 10, further comprising fractionating the xylenes fraction to form a stream containing C₉-C₁₀ alkylaromatic compounds, mixing that stream with the dehydrogenated stream of step (d), and contacting the mixture with the transalkylation catalyst.

15. A method for efficiently using hydrogen in aromatics production from heavy aromatic oil, said method comprising:

(a) contacting a hydrocarbonaceous stream comprising C₉⁺ hydrocarbons and an essentially pure hydrogen stream serially with a hydrotreating catalyst under hydrotreating conditions and a hydrocracking catalyst under hydrocracking conditions in a hydrocracking zone and, respectively, to produce a hydrocracking zone effluent comprising xylenes;

(b) fractionating the hydrocracking zone effluent in a fractionation zone to separately recover a first stream of hydrocarbons comprising C₄ and lighter hydrocarbons, a second stream of hydrocarbons comprising hydrocarbons boiling below about 195°

F., a third stream comprising hydrocarbons boiling between about 180°

F. and about 380°

F., and a fourth stream comprising diesel;

(c) introducing a low purity hydrogen-containing stream to the third stream from step (b) to form a combined stream and heating the combined stream to form a heated combination;

(d) contacting the heated combination with a transalkylation catalyst to form an effluent comprising hydrogen, volatile compounds, and aromatics;

(e) separating the hydrogen and volatile components from the aromatics to form a gaseous stream and an aromatic-containing stream;

(f) subjecting the gaseous stream to pressure swing adsorption to provide an essentially pure hydrogen-containing stream;

(g) increasing the pressure on the essentially pure hydrogen-containing stream and introducing it to the hydrocracking zone of step (a); and

(h) recovering the liquid hydrocarbon products in the aromatic-containing stream.

16. The method of claim 15, further comprising fractionating the aromatics-containing stream of step (h) to form a benzene fraction, a toluene fraction, and a xylenes fraction.

17. The method of claim 15, further comprising recycling the toluene fraction to the transalkylation reactor.

18. The method of claim 16, further comprising recycling the toluene fraction to the transalkylation reactor.

19. The method of claim 15, further comprising fractionating the xylenes fraction to form a stream containing C₉-C₁₀ alkylaromatic compounds, mixing that stream with the dehydrogenated stream of step (d), and contacting the mixture with the transalkylation catalyst.

20. The method of claim 16, further comprising fractionating the xylenes fraction to form a stream containing C₉-C₁₀ alkylaromatic compounds, mixing that stream with the dehydrogenated stream of step (d), and contacting the mixture with the transalkylation catalyst.