IPC분류정보
국가/구분 |
United States(US) Patent
등록
|
국제특허분류(IPC7판) |
|
출원번호 |
US-0538886
(2003-12-12)
|
등록번호 |
US-8123932
(2012-02-28)
|
우선권정보 |
IT-MI2002A2713 (2002-12-20); IT-MI2003A0692 (2003-04-08) |
국제출원번호 |
PCT/EP03/14545
(2003-12-12)
|
§371/§102 date |
20060324
(20060324)
|
국제공개번호 |
WO2004/056947
(2004-07-08)
|
발명자
/ 주소 |
- Montanari, Romolo
- Marchionna, Mario
- Panariti, Nicoletta
- Delbianco, Alberto
- Rosi, Sergio
|
출원인 / 주소 |
|
대리인 / 주소 |
Oblon, Spivak, McClelland, Maier & Neustadt, L.L.P.
|
인용정보 |
피인용 횟수 :
6 인용 특허 :
7 |
초록
▼
A process for the conversion of heavy feedstocks using hydrotreatment, distillation or flash, and deasphalting that includes mixing a heavy feedstock with a hydrogenation catalyst and subjecting the thus-formed mixture to a hydrotreatment reactor for reaction with one or more of hydrogen and hydroge
A process for the conversion of heavy feedstocks using hydrotreatment, distillation or flash, and deasphalting that includes mixing a heavy feedstock with a hydrogenation catalyst and subjecting the thus-formed mixture to a hydrotreatment reactor for reaction with one or more of hydrogen and hydrogen sulfide to form a first product stream; subjecting the first product stream to a distillation or flash to form a plurality of distillate fractions; and recycling heavies from the distillation residue and/or tar by deasphalting in the presence of a solvent; where the hydrotreatment reaction product is pre-separated under high pressure to form light and heavy fractions and sending the heavy fraction to the distillation and/or flash.
대표청구항
▼
1. A process for the conversion of a heavy feedstock selected from the group consisting of heavy crude oils, distillation residues, heavy oils coming from catalytic treatment, thermal tars, bitumens from oil sands, coals and high-boiling feedstocks of a hydrocarbon origin known as black oils, includ
1. A process for the conversion of a heavy feedstock selected from the group consisting of heavy crude oils, distillation residues, heavy oils coming from catalytic treatment, thermal tars, bitumens from oil sands, coals and high-boiling feedstocks of a hydrocarbon origin known as black oils, including the combined three process units: hydroconversion with catalysts in slurry phase, distillation or flash, and deasphalting, said method comprising: mixing at least part of the heavy feedstock and/or at least most of a stream containing asphaltenes obtained from a deasphalting unit with a suitable hydrogenation catalyst to form a first mixture and sending the first mixture to a hydrotreatment reactor into which hydrogen or a mixture of hydrogen and H2S is charged to form a hydrotreatment reaction product;sending a stream containing the hydrotreatment reaction product and the catalyst in dispersed phase to one or more distillation or flash units whereby one or more different fractions coming from the hydrotreatment reaction product are separated and a distillation residue or liquid comprising the catalyst in dispersed phase and which is rich in metal sulfides produced by demetallation of the feedstock is formed;recycling at least part of the distillation residue or liquid, to a deasphalting zone in the presence of solvents, optionally also fed with at least a fraction of the heavy feedstock, to form a second stream and a third stream, wherein the second stream comprises deasphalted oil and the third stream comprises other asphaltenes, wherein the stream containing the hydrotreatment reaction product and the catalyst in dispersed phase, before being sent to one or more distillation or flash units, is subjected to a high pressure separation pre-step in order to obtain a light fraction and a heavy fraction, the heavy fraction alone being sent to said distillation unit; andwherein the light fraction obtained by the high pressure separation pre-step is sent to a secondary hydrogenation post-treatment section, to produce a lighter fraction containing C1-C4 gas and H2S and a heavier fraction containing hydrotreated naphtha and gas oil. 2. The process according to claim 1, wherein the hydrogenation post-treatment reaction is effected at a pressure ranging from 7 to 14 MPa. 3. The process according to claim 1, wherein all the heavy feedstock is mixed with a suitable hydrogenation catalyst and sent to the hydrotreatment reactor, whereas at least 60% of the stream containing asphaltenes, which also contains catalyst in dispersed phase and is enriched with metals coming from the initial feedstock, is recycled to the hydrotreatment zone. 4. The process according to claim 3, wherein at least 80% of the stream containing asphaltenes is recycled to the hydrotreatment zone. 5. The process according to claim 1, wherein part of the heavy feedstock and at least most of the stream containing asphaltenes, which also contains catalyst in dispersed phase, are mixed with a suitable hydrogenation catalyst and sent to the hydrotreatment reactor, whereas the remaining part of the heavy feedstock is sent to the deasphalting zone. 6. The process according to claim 1, wherein at least most of the third stream containing asphaltenes, which essentially consists of said asphaltenes, is mixed with a suitable hydrogenation catalyst and sent to the hydrotreatment reactor, whereas all the heavy feedstock is fed to the deasphalting zone. 7. The process according to claim 1, wherein part of the distillation residue or liquid leaving the flash unit is recycled to the deasphalting zone and at least part of the remaining part of said distillation or flash residue is sent to the hydrotreatment reactor. 8. The process according to claim 7, wherein at least part of the distillation or flash residue is sent to the hydrotreatment reactor together with at least part of the stream containing asphaltenes coming from the deasphalting zone. 9. The process according to claim 1, wherein at least 80% by weight of the distillation residue is recycled to the deasphalting zone. 10. The process according to claim 9, wherein at least 95% by weight of the distillation residue is recycled to the deasphalting zone. 11. The process according to claim 1, wherein at least part of the remaining quantity of distillation residue, not recycled to the deasphalting zone is recycled to the hydrotreatment section. 12. The process according to claim 1, wherein the distillation unit is operated at a reduced pressure ranging from 0.0001 to 0.5 MPa. 13. The process according to claim 12, wherein the distillation unit is operated at a reduced pressure ranging from 0.001 to 0.3 MPa. 14. The process according to claim 1, wherein the hydrotreatment unit is operated at a temperature ranging from 370 to 480° C. and at a pressure ranging from 3 to 30 MPa. 15. The process according to claim 14, wherein the hydrotreatment unit is operated at a temperature ranging from 380 to 440° C. and at a pressure ranging from 10 to 20 MPa. 16. The process according to claim 1, wherein the deasphalting unit is operated at temperature ranging from 40 to 200° C. and at a pressure ranging from 0.1 to 7 MPa. 17. The process according to claim 1, wherein the deasphalting solvent is a light paraffin with from 3 to 7 carbon atoms. 18. The process according to claim 1, wherein the deasphalting unit is operated under subcritical or supercritical conditions with one or more steps. 19. The process according to claim 1, wherein the second stream comprising deasphalted oil is fractionated by means of conventional distillation. 20. The process according to claim 1, wherein the second stream comprising deasphalted oil is mixed with the products separated in the distillation step after being condensed. 21. The process according to claim 1, wherein the hydrogenation catalyst is a decomposable precursor or a preformed compound based on one or more transition metals. 22. The process according to claim 21, wherein the transition metal is molybdenum. 23. The process according to claim 1, wherein the concentration of the catalyst in the hydroconversion reactor, defined on the basis of the concentration of the metal or metals present, ranges from 300 to 20000 ppm. 24. The process according to claim 23, wherein the concentration of the catalyst in the hydroconversion reactor ranges from 1000 to 10000 ppm. 25. The process according to claim 1, wherein a fraction of the third stream containing asphaltenes, coming from the deasphalting zone, called flushing stream, is sent to a treatment section with a suitable solvent for the separation of the product into a solid fraction and a liquid fraction from which said solvent can be subsequently separated. 26. The process according to claim 25, wherein the flushing stream is in a quantity ranging from 0.5 to 10% by volume with respect to the feedstock. 27. The process according to claim 25, wherein at least part of the liquid fraction deriving from the treatment section of the flushing is sent as such or after being separated from the solvent and/or after the addition of a suitable fluxing liquid to the Fuel Oil fraction. 28. The process according to claim 27, wherein at least part of the liquid fraction deriving from the treatment section of the flushing is recycled to the hydrotreatment reactor. 29. The process according to claim 25, wherein the solvent used in the treatment section of the flushing is an aromatic solvent or a mixture of gas oils produced in the process itself or available in refineries. 30. The process according to claim 29, wherein the aromatic solvent is toluene and/or xylene blends. 31. The process according to claim 25, wherein the volumetric ratio solvent/flushing stream varies from 1 to 10. 32. The process according to claim 31, wherein the volumetric ratio solvent/flushing stream varies from 1 to 5. 33. The process according to claim 32, wherein the volumetric ratio solvent/flushing stream varies from 1.5 to 3.5. 34. The process according to claim 25, wherein the hydrogenation catalyst is a decomposable precursor or a preformed compound based on one or more transition metals and the solid fraction of the solid treated is sent to a further selective recovery treatment of the transition metal(s) contained in the hydrogenation catalyst. 35. The process according to claim 34, wherein the transition metal(s) recovered, is recycled to the hydrotreatment reactor. 36. The process according to claim 34, wherein the second stream consists of deasphaltated oil. 37. The process according to claim 1, wherein the first mixture is sent directly to the hydrotreatment reactor. 38. The process according to claim 1, wherein the high pressure separation pre-step forms only the lighter fraction and the heavier fraction, and the distillation forms only the distillation residue or liquid comprising the catalyst and one overhead fraction. 39. The process according to claim 1, wherein the high pressure separation pre-step forms only the lighter fraction and the heavier fraction, and the entire amount of the lighter fraction is hydrotreated in the secondary hydrogenation post-treatment section. 40. The process according to claim 1, wherein the high pressure separation pre-step is carried out at a pressure of from 3-14 MPa.
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