Process for upgrading heavy oil using a reactor with a novel reactor separation system

Abstract
Applicants have developed a new residuum full hydroconversion slurry reactor system that allows the catalyst, unconverted oil, hydrogen, and converted oil to circulate in a continuous mixture throughout an entire reactor with no confinement of the mixture. The mixture is separated internally, within one of more of the reactors, to separate only the converted oil and hydrogen into a vapor product while permitting the unconverted oil and the slurry catalyst to continue on into the next sequential reactor as a liquid product. A portion of the unconverted oil is then converted to lower boiling point hydrocarbons in the next reactor, once again creating a mixture of unconverted oil, hydrogen, converted oil, and slurry catalyst. Further hydroprocessing may occur in additional reactors, fully converting the oil. The oil may alternately be partially converted, leaving a concentrated catalyst in unconverted oil which can be recycled directly to the first reactor.
Description
FIELD OF THE INVENTION

The instant invention relates to a process for upgrading heavy oils using a slurry catalyst composition.


BACKGROUND OF THE INVENTION

There is an increased interest at this time in the processing of heavy oils, due to larger worldwide demand for petroleum products. Canada and Venezuela are sources of heavy oils. Processes which result in complete conversion of heavy oil feeds to useful products are of particular interest.


U.S. Pat. No. 6,278,034 recites a hydrogenation process which employs a reactor having an internal means of separating gaseous product from a slurry of oil and catalyst.


The following patent applications, which are incorporated by reference, are directed to the preparation of highly active slurry catalyst compositions and their use in processes for upgrading heavy oil:


U.S. Ser. No. 10/938,202 is directed to the preparation of a catalyst composition suitable for the hydroconversion of heavy oils. The catalyst composition is prepared by a series of steps, involving mixing a Group VIB metal oxide and aqueous ammonia to form an aqueous mixture, and sulfiding the mixture to form a slurry. The slurry is then promoted with a Group VIII metal. Subsequent steps involve mixing the slurry with a hydrocarbon oil and combining the resulting mixture with hydrogen gas and a second hydrocarbon oil having a lower viscosity than the first oil. An active catalyst composition is thereby formed.


U.S. Ser. No. 10/938,003 is directed to the preparation of a slurry catalyst composition. The slurry catalyst composition is prepared in a series of steps, involving mixing a Group VIB metal oxide and aqueous ammonia to form an aqueous mixture and sulfiding the mixture to form a slurry. The slurry is then promoted with a Group VIII metal. Subsequent steps involve mixing the slurry with a hydrocarbon oil, and combining the resulting mixture with hydrogen gas (under conditions which maintain the water in a liquid phase) to produce the active slurry catalyst.


U.S. Ser. No. 10/938,438 is directed to a process employing slurry catalyst compositions in the upgrading of heavy oils. The slurry catalyst composition is not permitted to settle, which would result in possible deactivation. The slurry is recycled to an upgrading reactor for repeated use and products require no further separation procedures for catalyst removal.


U.S. Ser. No. 10/938,200 is directed to a process for upgrading heavy oils using a slurry composition. The slurry composition is prepared in a series of steps, involving mixing a Group VIB metal oxide with aqueous ammonia to form an aqueous mixture and sulfiding the mixture to form a slurry. The slurry is then promoted with a Group VIII metal compound. Subsequent steps involve mixing the slurry with a hydrocarbon oil, and combining the resulting mixture with hydrogen gas (under conditions which maintain the water in a liquid phase) to produce the active slurry catalyst.


U.S. Ser. No. 10/938,269 is directed to a process for upgrading heavy oils using a slurry composition. The slurry composition is prepared by a series of steps, involving mixing a Group VIB metal oxide and aqueous ammonia to form an aqueous mixture, and sulfiding the mixture to form a slurry. The slurry is then promoted with a Group VIII metal. Subsequent steps involve mixing the slurry with a hydrocarbon oil and combining the resulting mixture with hydrogen gas and a second hydrocarbon oil having a lower viscosity than the first oil. An active catalyst composition is thereby formed.


SUMMARY OF THE INVENTION

A process for the hydroconversion of heavy oils, said process employing an upflow reactor with a separator located internally to do phase separation. At least one reactor with an internal separator may be employed, although it is more common to use reactors in series. A hydroconversion process with reactors in series may employ the following steps: (a) combining a heated heavy oil feed, an active slurry catalyst composition and a hydrogen-containing gas to form a mixture; (b) passing the mixture of step (a) to the bottom of a reactor, which is maintained at hydroprocessing conditions, including elevated temperature and pressure; (c) separating internally in the reactor a stream comprising reaction products, hydrogen gas, unconverted oil, and slurry catalyst into two streams, a vapor stream comprising reaction products and hydrogen, and a liquid stream comprising unconverted material and slurry catalyst; (d) passing the vapor stream overhead to further processing, and passing at least a portion of the liquid stream, to the next reactor in series.


This invention is intended to perform phase separation within one or more reactors in the process scheme depicted, so that a single vapor phase product is the only product leaving the top of the reactor. A liquid phase product is the only stream leaving the lower portion of the reactor (through the bottom or side) for further processing. If internal separation occurs, there is no need for a hot high pressure separator or flash drum to separate the phase following their exit from the reactor.


The instant invention further employs a reactor differential pressure control system that regulates the vapor product leaving the top of the reactor, thus making a control valve on the feed stream to the next reactor unnecessary.





BRIEF DESCRIPTION OF THE FIGURE

The FIGURE shows the process scheme of this invention as applied to a multiple reactor system in series.





DETAILED DESCRIPTION OF THE INVENTION

The instant invention is directed to a process for catalyst activated slurry hydrocracking. Interstage separation of gaseous reaction products and liquid streams comprising uncoverted oil and catalyst is effective in maintaining heat balance in the process. In the FIGURE, stream 1 comprises a heavy feed, such as vacuum residuum. Other feeds may include atmospheric residuum, vacuum residuum, tar from a solvent deasphalting unit, atmospheric gas oils, vacuum gas oils, deasphalted oils, olefins, oils derived from tar sands or bitumen, oils derived from coal, heavy crude oils, synthetic oils from Fischer-Tropsch processes, and oils derived from recycled oil wastes and polymers.


The feed enters furnace 80 where it is heated, exiting in stream 4. Stream 4 combines with a hydrogen containing gas (stream 2), recycle slurry (stream 17), and a stream comprising an active slurry composition (stream 3), resulting in a mixture (stream 24). Stream 24 enters the bottom of the first reactor 10. Vapor Stream 31 exits the top of the reactor comprising primarily reaction products and hydrogen, due to a separation apparatus inside the reactor (not shown). Liquid stream 26, which contains slurry in combination with unconverted oil, exits the bottom, or side, of reactor 10.


Stream 26 is combined with a gaseous stream comprising hydrogen (steam 15) to create stream 27. Stream 27 enters the bottom of second reactor 20.


Vapor stream 8, comprising primarily reaction products and hydrogen, exits the top of the reactor 20 and joins the vapor product from reactor 20. Liquid stream 27, which contains slurry in combination with unconverted oil, exits the bottom, or side, of reactor 20.


Stream 32 is combined with a gaseous stream comprising hydrogen (stream 16) to create stream 28. Stream 28 enters the bottom of reactor 30. Vapor stream 12, comprising primarily reaction products and hydrogen, exits the top of the reactor and joins the vapor product from the first two reactors in stream 14. Liquid stream 17, which contains slurry in combination with unconverted oil, exits the bottom, or side, of reactor 30. A portion of this stream may be drawn off as stream 18 or recycled back to the first reactor 10, as stream 17.


Overhead streams from reactors 10, 20 and 30 (streams 31, 8 and 12 respectively) create stream 14, which passes to downstream equipment for further processing.


The preferred type of reactor in the instant invention is a liquid recirculating reactor, although other types of upflow reactors may be employed. Liquid recirculating reactors are discussed further in copending application Ser. No. 11/305,359 or US Patent Publication No. US2007140927 (T-6493), which is incorporated by reference.


A liquid recirculation reactor is an upflow reactor which feeds heavy hydrocarbon oil and a hydrogen rich gas at elevated pressure and temperature for hydroconversion. Process conditions for the liquid recirculating reactor include pressures in the range from 1500 through 3500 psia, preferably 2000 through 3000 psia. Temperatures are in the range from 700 through 900 F, preferably 775 through 850 F.


Hydroconversion includes processes such as hydrocracking and the removal of heteroatom contaminants (such sulfur and nitrogen). In slurry catalyst use, catalyst particles are extremely small (1-10 micron). Pumps may be used for recirculation of slurry, although they not required to be used.


The process for the preparation of the catalyst slurry composition used in this invention is set forth in U.S. Ser. No. 10/938,003 and U.S. Ser. No. 10/938,202 and is incorporated by reference. The catalyst composition is useful for but not limited to hydrogenation upgrading processes such as hydrocracking, hydrotreating, hydrodesulphurization, hydrodenitrification, and hydrodemetallization.

Claims
  • 1. A process for the hydroconversion of heavy oils, said process comprising the following steps: (a) providing at least two upflow reactors, a first reactor and a second reactor, with a separator located internally in at least one reactor;(b) combining a heated heavy oil feed, an active slurry catalyst composition having particle sizes of 1-10 micron and a hydrogen-containing gas to form a mixture;(c) passing the mixture of step (b) to the bottom of the first reactor, which is maintained at a temperature from 700 to 900 F and a pressure from 1500 to 3500 psia;(d) separating internally in the first reactor a stream comprising reaction product, hydrogen gases, unconverted material and slurry catalyst into two streams, a vapor stream comprising reactor products and hydrogen, and a liquid stream comprising unconverted material and slurry catalyst;(e) passing the vapor stream overhead to further processing, and passing the liquid stream, comprising unconverted material and slurry catalyst, from the first reactor as a bottoms stream;(f) passing at least a portion of the liquid stream of step (e) to the bottom of the second reactor, which is maintained at hydroprocessing conditions, including elevated temperature and pressure;(g) separating internally in the second reactor a stream comprising reaction product, hydrogen gases, unconverted material and slurry catalyst into two streams, a vapor stream comprising reactor products and hydrogen, and a liquid stream comprising unconverted material and slurry catalyst;(h) passing the vapor stream overhead to further processing, and passing the liquid stream, comprising unconverted material and slurry catalyst, from the second reactor as a bottoms stream to further processing;wherein the heavy oil is selected from the group consisting of atmospheric residuum, vacuum residuum, tar from a solvent deasphlating unit, oils derived from tar sands or bitumen, oils derived from coal, heavy crude oils, and oils derived from recycled oil wastes and polymers.
  • 2. The process of claim 1, wherein the liquid stream of step (h) is recycled to step (b), the mixture of step (b) further comprising recycled unconverted material and slurry catalyst.
  • 3. The process of claim 1, in which the upflow reactor is a recirculating reactor which employs a pump for recirculating of the slurry.
  • 4. The process of claim 1, in which the pressure is from 2000 through 3000 psia and the temperature is from 775 through 850 F.
  • 5. The hydroconversion process of claim 1, wherein the process is selected from the group consisting of hydrocracking, hydrotreating, hydrodesulphurization, hydrodenitrification, and hydrodemetalization.
  • 6. The process of claim 1, wherein the active slurry catalyst composition of claim 1 is prepared by the following steps: (a) mixing a Group VIB metal oxide and aqueous ammonia to form a Group VIB metal compound aqueous mixture;(b) sulfiding, in an initial reaction zone, the aqueous mixture of step (a) with a gas comprising hydrogen sulfide to a dosage greater than 8 SCF of hydrogen sulfide per pound of Group VIB metal to form a slurry;(c) promoting the slurry with a Group VIII metal compound;(d) mixing the slurry of step (c) with a hydrocarbon oil having a viscosity of at least 2 cSt@ 212° F. to form an intermediate mixture;(e) combining the intermediate mixture with hydrogen gas in a second reaction zone, under conditions which maintain the water in the intermediate mixture in a liquid phase, thereby forming an active catalyst composition admixed with a liquid hydrocarbon; and(f) recovering the active catalyst composition.
  • 7. The process of claim 1, in which at least 90 wt % of the feed is converted to lower boiling products.
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 11/303,427 with a filing date of Dec. 16, 2005 now U.S. Pat. No. 7,431,822, the disclosure of which is incorporated herein by reference.

US Referenced Citations (126)
Number Name Date Kind
3817856 Aaron et al. Jun 1974 A
4485004 Fisher et al. Nov 1984 A
4592827 Galiasso et al. Jun 1986 A
4684456 Van Driesen et al. Aug 1987 A
4710486 Lopez et al. Dec 1987 A
4824821 Lopez et al. Apr 1989 A
4943547 Seamans et al. Jul 1990 A
4970190 Lopez et al. Nov 1990 A
5039392 Bearden et al. Aug 1991 A
5041404 Seamans et al. Aug 1991 A
5162282 Lopez et al. Nov 1992 A
5164075 Lopez et al. Nov 1992 A
5178749 Lopez et al. Jan 1993 A
5298152 Kramer et al. Mar 1994 A
5371308 Gosselink et al. Dec 1994 A
5374348 Sears et al. Dec 1994 A
5484755 Lopez et al. Jan 1996 A
5527473 Ackerman Jun 1996 A
5871638 Pradhan et al. Feb 1999 A
5914010 Hood et al. Jun 1999 A
5925238 Duddy et al. Jul 1999 A
5935418 Chakrabarty et al. Aug 1999 A
5954945 Cayton et al. Sep 1999 A
5977192 Howsmon et al. Nov 1999 A
6071402 Danot et al. Jun 2000 A
6139723 Pelrine et al. Oct 2000 A
6156693 Song et al. Dec 2000 A
6156695 Soled et al. Dec 2000 A
6162350 Soled et al. Dec 2000 A
6190542 Comolli et al. Feb 2001 B1
6241874 Wallace et al. Jun 2001 B1
6270654 Colyar et al. Aug 2001 B1
6274530 Cayton et al. Aug 2001 B1
6277895 Zhou et al. Aug 2001 B1
6278034 Espinoza et al. Aug 2001 B1
6291391 MacArthur et al. Sep 2001 B1
6299760 Soled et al. Oct 2001 B1
6451729 Song et al. Sep 2002 B1
6534437 Eijsbouts et al. Mar 2003 B2
6554994 Reynolds et al. Apr 2003 B1
6620313 Demmin et al. Sep 2003 B1
6630066 Cash et al. Oct 2003 B2
6635599 Eijsbouts et al. Oct 2003 B1
6652738 Eijsbouts et al. Nov 2003 B2
6660157 Que et al. Dec 2003 B2
6712955 Hou et al. Mar 2004 B1
6726832 Baldassari et al. Apr 2004 B1
6758963 Hantzer et al. Jul 2004 B1
7150823 Mayer et al. Dec 2006 B2
7179366 Harle et al. Feb 2007 B2
7214308 Colyar May 2007 B2
7223713 Alonso et al. May 2007 B2
7232515 Demmin et al. Jun 2007 B1
7297250 Bronicki Nov 2007 B2
7358413 Stell et al. Apr 2008 B2
7413669 Gonzalez et al. Aug 2008 B2
7416653 Wellington et al. Aug 2008 B2
20020010088 Eijsbouts et al. Jan 2002 A1
20020125172 Que et al. Sep 2002 A1
20020166797 Banerjee Nov 2002 A1
20030089636 Marchionna et al. May 2003 A1
20030102254 Eijsbouts et al. Jun 2003 A1
20030150778 Haluska et al. Aug 2003 A1
20040134837 Dassori et al. Jul 2004 A1
20040163999 Plantega et al. Aug 2004 A1
20040226860 Bourges et al. Nov 2004 A1
20050040080 Riley et al. Feb 2005 A1
20050145538 Wellington et al. Jul 2005 A1
20050145543 Bhan et al. Jul 2005 A1
20050150818 Bhan et al. Jul 2005 A1
20050155908 Bhan et al. Jul 2005 A1
20050167320 Bhan et al. Aug 2005 A1
20050167321 Wellington et al. Aug 2005 A1
20050167322 Wellington et al. Aug 2005 A1
20050167323 Wellington et al. Aug 2005 A1
20050167324 Bhan et al. Aug 2005 A1
20050167326 Bhan et al. Aug 2005 A1
20050167327 Bhan et al. Aug 2005 A1
20050167328 Bhan et al. Aug 2005 A1
20050167329 Bhan et al. Aug 2005 A1
20050167330 Bhan et al. Aug 2005 A1
20050167331 Bhan et al. Aug 2005 A1
20050167332 Bhan et al. Aug 2005 A1
20050173298 Wellington et al. Aug 2005 A1
20050173301 Bhan et al. Aug 2005 A1
20050173302 Bhan et al. Aug 2005 A1
20050173303 Bhan et al. Aug 2005 A1
20050241992 Lott et al. Nov 2005 A1
20050241993 Lott et al. Nov 2005 A1
20060011511 Hokari et al. Jan 2006 A1
20060054535 Chen et al. Mar 2006 A1
20060060501 Gauthier et al. Mar 2006 A1
20060060502 Soled et al. Mar 2006 A1
20060060503 Soled et al. Mar 2006 A1
20060157385 Montanari et al. Jul 2006 A1
20060163115 Montanari et al. Jul 2006 A1
20060175229 Montanari et al. Aug 2006 A1
20060186021 Marchionna et al. Aug 2006 A1
20060201854 Lott et al. Sep 2006 A1
20060207917 Domokos et al. Sep 2006 A1
20060231465 Bhan et al. Oct 2006 A1
20060272982 Montanari et al. Dec 2006 A1
20060289340 Brownscombe et al. Dec 2006 A1
20070000808 Bhan et al. Jan 2007 A1
20070000810 Bhan et al. Jan 2007 A1
20070012595 Brownscombe et al. Jan 2007 A1
20070045156 Khadzhiev et al. Mar 2007 A1
20070084754 Soled et al. Apr 2007 A1
20070090023 Soled et al. Apr 2007 A1
20070090024 Soled et al. Apr 2007 A1
20070158236 Zhou et al. Jul 2007 A1
20070158238 Wu et al. Jul 2007 A1
20070161505 Pereira-Almao et al. Jul 2007 A1
20070238607 Alonso et al. Oct 2007 A1
20070284285 Stepanik et al. Dec 2007 A1
20070295641 Brownscombe et al. Dec 2007 A1
20070295645 Brownscombe et al. Dec 2007 A1
20070295646 Bhan et al. Dec 2007 A1
20070295647 Brownscombe et al. Dec 2007 A1
20080083650 Bhan et al. Apr 2008 A1
20080083652 Morel et al. Apr 2008 A1
20080083655 Bhan et al. Apr 2008 A1
20080085225 Bhan et al. Apr 2008 A1
20080087575 Bhan et al. Apr 2008 A1
20080087578 Bhan et al. Apr 2008 A1
20080099371 McCoy et al. May 2008 A1
Related Publications (1)
Number Date Country
20090057194 A1 Mar 2009 US
Continuations (1)
Number Date Country
Parent 11303427 Dec 2005 US
Child 12212231 US