EP0432235A1 - Process for the production of improved octane numbers gasolines. - Google Patents
Process for the production of improved octane numbers gasolines.Info
- Publication number
- EP0432235A1 EP0432235A1 EP90908440A EP90908440A EP0432235A1 EP 0432235 A1 EP0432235 A1 EP 0432235A1 EP 90908440 A EP90908440 A EP 90908440A EP 90908440 A EP90908440 A EP 90908440A EP 0432235 A1 EP0432235 A1 EP 0432235A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- hydrocarbons
- gasolines
- boiling
- clo
- lco
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 title description 7
- 238000009835 boiling Methods 0.000 claims abstract description 36
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 33
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 33
- 238000004523 catalytic cracking Methods 0.000 claims abstract description 23
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 19
- 239000003054 catalyst Substances 0.000 claims description 25
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 238000004231 fluid catalytic cracking Methods 0.000 claims description 3
- 239000000686 essence Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 239000003502 gasoline Substances 0.000 abstract description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 239000007789 gas Substances 0.000 description 7
- 239000010457 zeolite Substances 0.000 description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- DDTIGTPWGISMKL-UHFFFAOYSA-N molybdenum nickel Chemical compound [Ni].[Mo] DDTIGTPWGISMKL-UHFFFAOYSA-N 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 229910003296 Ni-Mo Inorganic materials 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000011959 amorphous silica alumina Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012013 faujasite Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- -1 gas oils Chemical class 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
- C10G69/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only
- C10G69/04—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only including at least one step of catalytic cracking in the absence of hydrogen
Definitions
- the present invention relates to a process for producing gasolines with a high octane number.
- the present invention relates to the production of gasoline having an improved RON and MON, starting from heavier hydrocarbon feeds, originating from the catalytic cracking in a fluidized bed of vacuum gasels, deasphalted oils and residues.
- the catalytic cracking process in a fluidized bed of heavy hydrocarbon feedstocks such as vacuum gas oils is a well-known process in particular for producing gasolines. It is also essential to produce gasolines with a high octane number due to the upcoming removal of lead additives. There is therefore a growing need to obtain, at the start of these same charges, gasolines having an octane index or RON indices (octane index "Research”) and particularly MON (octane index "Engine”) improved.
- the object of the present invention is a process which makes it possible to produce gasolines having improved RON and MON starting from heavy hydrocarbon charges.
- the present invention also aims at a process for producing gasolines having improved RON and MON, from hydrogenated LCO, HCO and CLO.
- the process of the present invention for producing gasolines having improved RON and MON is characterized in that it comprises the steps which consist in: a. Subject to a catalytic cracking in a fluidized bed, a charge of heavy hydrocarbons, by contacting with a fluid catalytic cracking catalyst, to form gaseous products, hydrocarbons boiling in the range of gasolines, LCOs, HCOs and CLO; b. Separate the catalyst from the products formed; vs.
- FIG. 1 represents a schematic diagram of the process of the invention.
- a charge of heavy hydrocarbons is introduced via line 10, which may consist of gas oil, vacuum gas oil or other similar charges.
- This charge is introduced into the FCC reactor 20 in which it is brought into contact with a fluid catalytic cracking catalyst introduced through line 22.
- the charge and the catalyst are mixed and driven upwards.
- the catalyst is made up of fine particles so that it acts as a fluidized bed.
- the reaction takes place in reactor 20, the catalyst falls by gravity and is recovered for regeneration by line 18 and is regenerated in reactor 16, while the various products of the catalytic reaction which include gaseous hydrocarbons, hydrocarbons boiling in the range of gasolines, LCOs, HCOs and CLOs are recovered via line 24, to be sent to a separator (25) to separate the gaseous and light products leaving through line 26, heavier products leaving through line 28.
- the light products recovered through line 26 consist of hydrocarbons boiling in the range of gasolines.
- the heavy products leaving via line 28 consist of LCO boiling between 221 and 350 ° C, HCO boiling between 350 and 400 ° C as well as CLO boiling at a temperature above 400 ° C.
- the LCO, the HCO and the CLO are successively separated and they are subjected separately afterwards to a hydrogenation treatment.
- the LCOs, HCOs and CLOs are subjected together to a hydrogenation treatment.
- the current leaving via line 28 is mixed with hydrogen coming from one or the other source defined below and the mixture of charge and hydrogen via line 29 in the hydrogenation reaction zone 30 in the presence of a hydrogenation catalyst at a temperature between 320 and 420 ° C and under a pressure between 30 and 200 bar.
- the hydrogenation catalyst is in the form of a fixed bed, in the reaction zone 30.
- the charge to be hydrogenated passes through the catalytic bed maintained under hydrogenation conditions as stated above.
- the effluent product is withdrawn from the reactor 30 via the line 31 and it is introduced into the separator 32, in which the gaseous products and products boiling in the range of gasoline are separated on the one hand by the line 33.
- the Applicant has unexpectedly found that by subjecting all of the hydrogenated products having a boiling point above 221 ° C. taken together or separately to an FCC, the total quantity of gasolines formed by the process is increased and the RON and MON of the species formed were considerably increased. It is understood that the process of the invention can be adapted to the numerous modes of execution of a catalytic cracking in a fluidized bed, the essential being to resubmit the hydrogenated hydrocarbons and boiling above 221 ° C., to a treatment. from FCC.
- the Applicant has moreover observed that subjecting the hydrogenated LCOs, HCOs and / or CLOs to a new FCC makes it possible to obtain gasolines with better RON and MON. Contrary to what is taught in the state of the art, it is not essential to limit the FCC reaction of LCOs, HCOs and / or CLOs with partially deactivated catalysts, in order to obtain the good gasoline yields, but, and this constitutes an essential element of the invention, it is absolutely necessary to contact it with a fresh FCC catalyst to obtain gasolines having a better RON and MON.
- the hydrocarbons leaving via line 34 can be recycled to the first FCC reactor (20) in admixture with the charge of VGO (vacuum stars), but the results from the RON and MON point of view of the species obtained are slightly lower than those obtained with the mode of execution of the method presented above.
- the FCC (20) can be used to crack the loads (normal heavy and hydrogenated LCO, HCO and / or CLO) by campaign.
- loads normal heavy and hydrogenated LCO, HCO and / or CLO
- catalysts suitable for use in catalytic cracking processes in particular amorphous silica-alumina, silica-magnesia, catalysts of the crystalline zeolite type such as faujasite or other analogues, such as Y zeolites dispersed in a matrix of silica and another inorganic oxide or in an alumina matrix.
- the zeolites can also be used pure with or without zeolitic promoters of the ZSM-5 or silicalite type.
- the matrices consist of silica-alumina in a 90-40 / 10-60 ratio, in which the zeolites are dispersed.
- Zeolites are generally of the Y zeolite type exchanged with rare earths or of the ultrastable type (the mode of dealumination being variable).
- Promoters can also be added in an amount of 5 to 15% by weight of the zeolite used.
- the catalytic cracking is generally carried out at temperatures between 480 and 550 ° C and preferably between 510 and 530 ° C; at pressures between 1 and 4 bar and preferably between 1 and 2 bar.
- the hydro-treatment catalyst is preferably resistant to sulfur. Most are Group VI and Group VIII metal catalysts deposited on an alumina or silica-alumina support and other similar supports. Most of the time, we use a Nickel-Molybdenum catalyst deposited on alumina or silica-alumina.
- the hydrogenation operating conditions are a temperature between 270 and 500 ° C, a pressure between 30 and 200 bars and preferably between 60 and 120 bars, an LHSV between 0.5 and 5 and a H2 / HC ratio included between 500 and 50,000 NL / L.
- VGO VGO
- the boiling products in the range of gasolines, LCOs and HCOs and CLOs were separated.
- the LCOs, HCOs and CLOs were subjected to hydrogenation separately in the presence of a Ni-Mo catalyst and under the conditions indicated in Table 1.
- the boiling products in the gasoline range were separated. and those with a boiling point of more than 221 ° C.
- the products having a boiling point above 221 ° C. were sent directly to a second catalytic cracking reactor under the conditions indicated in Table 1.
- the properties of the gasolines produced at the outlet of this latter catalytic cracking reactor are indicated in Table 1.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
On décrit un procédé pour produire des essences ayant des RON et MON améliorés, qui consiste à soumettre les LCO, HCO et CLO obtenus par craquage catalytique d'une charge d'hydrocarbures lourds, à un traitement d'hydrogénation et à soumettre ensuite les produits obtenus à un nouveau craquage catalytique et à récupérer finalement les hydrocarbures formés bouillant dans la gamme des essences.A process is described for producing gasolines having improved RON and MON, which consists in subjecting the LCO, HCO and CLO obtained by catalytic cracking of a load of heavy hydrocarbons, to a hydrogenation treatment and then subjecting the products obtained to a new catalytic cracking and to finally recover the hydrocarbons formed boiling in the gasoline range.
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE8900630A BE1004277A4 (en) | 1989-06-09 | 1989-06-09 | Method for producing species index ron and improved my. |
BE8900630 | 1989-06-09 | ||
PCT/BE1990/000028 WO1990015121A1 (en) | 1989-06-09 | 1990-06-08 | Process for the production of petrol with improved octane numbers |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0432235A1 true EP0432235A1 (en) | 1991-06-19 |
EP0432235B1 EP0432235B1 (en) | 1994-09-14 |
Family
ID=3884201
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90908440A Expired - Lifetime EP0432235B1 (en) | 1989-06-09 | 1990-06-08 | Process for the production of improved octane numbers gasolines |
Country Status (9)
Country | Link |
---|---|
US (1) | US5152883A (en) |
EP (1) | EP0432235B1 (en) |
JP (1) | JPH04500231A (en) |
AT (1) | ATE111507T1 (en) |
BE (1) | BE1004277A4 (en) |
DE (1) | DE69012526T2 (en) |
DK (1) | DK0432235T3 (en) |
ES (1) | ES2060172T3 (en) |
WO (1) | WO1990015121A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2597135A1 (en) * | 2011-11-24 | 2013-05-29 | IFP Energies nouvelles | Method for generating middle distillates from a conventional heavy feedstock including a step of selective hydrogenation of the HCO EX FCC cut |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5770044A (en) * | 1994-08-17 | 1998-06-23 | Exxon Research And Engineering Company | Integrated staged catalytic cracking and hydroprocessing process (JHT-9614) |
US5582711A (en) * | 1994-08-17 | 1996-12-10 | Exxon Research And Engineering Company | Integrated staged catalytic cracking and hydroprocessing process |
US5770043A (en) * | 1994-08-17 | 1998-06-23 | Exxon Research And Engineering Company | Integrated staged catalytic cracking and hydroprocessing process |
US6113776A (en) * | 1998-06-08 | 2000-09-05 | Uop Llc | FCC process with high temperature cracking zone |
US5944982A (en) | 1998-10-05 | 1999-08-31 | Uop Llc | Method for high severity cracking |
US6123830A (en) * | 1998-12-30 | 2000-09-26 | Exxon Research And Engineering Co. | Integrated staged catalytic cracking and staged hydroprocessing process |
EP1050572A3 (en) * | 1999-05-05 | 2001-06-06 | Bar-Co Processes Joint Venture | Residual oil fluid catalytic cracking process |
US6569316B2 (en) | 2000-04-17 | 2003-05-27 | Exxonmobil Research And Engineering Company | Cycle oil conversion process incorporating shape-selective zeolite catalysts |
US20010042702A1 (en) | 2000-04-17 | 2001-11-22 | Stuntz Gordon F. | Cycle oil conversion process |
US6569315B2 (en) | 2000-04-17 | 2003-05-27 | Exxonmobil Research And Engineering Company | Cycle oil conversion process |
US6565739B2 (en) | 2000-04-17 | 2003-05-20 | Exxonmobil Research And Engineering Company | Two stage FCC process incorporating interstage hydroprocessing |
US20010042701A1 (en) | 2000-04-17 | 2001-11-22 | Stuntz Gordon F. | Cycle oil conversion process |
US20070289899A1 (en) * | 2006-06-14 | 2007-12-20 | Fina Technology, Inc. | Stacked bed hydrotreating reactor system |
CN101210200B (en) | 2006-12-27 | 2010-10-20 | 中国石油化工股份有限公司 | Hydrogenation treatment and catalytic cracking combined process for residual oil |
US9309467B2 (en) | 2007-12-20 | 2016-04-12 | China Petroleum And Chemical Corp. | Integrated process for hydrogenation and catalytic cracking of hydrocarbon oil |
KR101503069B1 (en) | 2008-10-17 | 2015-03-17 | 에스케이이노베이션 주식회사 | Production of valuable aromatics and olefins from FCC light cycle oil |
JP5339845B2 (en) * | 2008-10-14 | 2013-11-13 | Jx日鉱日石エネルギー株式会社 | Fluid catalytic cracking method |
CN102361959B (en) | 2009-03-27 | 2014-07-30 | 吉坤日矿日石能源株式会社 | Method for producing aromatic hydrocarbons |
US20110163001A1 (en) * | 2010-01-07 | 2011-07-07 | Lourenco Jose J P | Upgrading heavy oil by deasphalting |
JP6278587B2 (en) | 2012-03-21 | 2018-02-14 | Jxtgエネルギー株式会社 | High aromatic base oil and method for producing high aromatic base oil |
US10626339B2 (en) | 2016-09-20 | 2020-04-21 | Uop Llc | Process and apparatus for recycling cracked hydrocarbons |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3172833A (en) * | 1965-03-09 | Catalytic conversion process for the production of low luminosity fuels | ||
US2243298A (en) * | 1939-02-24 | 1941-05-27 | Universal Oil Prod Co | Process for the manufacture of gasoline and iso-octane |
US3489673A (en) * | 1967-11-03 | 1970-01-13 | Universal Oil Prod Co | Gasoline producing process |
US3755141A (en) * | 1971-02-11 | 1973-08-28 | Texaco Inc | Catalytic cracking |
US4426276A (en) * | 1982-03-17 | 1984-01-17 | Dean Robert R | Combined fluid catalytic cracking and hydrocracking process |
US4585545A (en) * | 1984-12-07 | 1986-04-29 | Ashland Oil, Inc. | Process for the production of aromatic fuel |
US4943366A (en) * | 1985-06-03 | 1990-07-24 | Mobil Oil Corporation | Production of high octane gasoline |
-
1989
- 1989-06-09 BE BE8900630A patent/BE1004277A4/en not_active IP Right Cessation
-
1990
- 1990-06-08 DK DK90908440.2T patent/DK0432235T3/en active
- 1990-06-08 JP JP2507877A patent/JPH04500231A/en active Pending
- 1990-06-08 WO PCT/BE1990/000028 patent/WO1990015121A1/en active IP Right Grant
- 1990-06-08 EP EP90908440A patent/EP0432235B1/en not_active Expired - Lifetime
- 1990-06-08 DE DE69012526T patent/DE69012526T2/en not_active Expired - Fee Related
- 1990-06-08 ES ES90908440T patent/ES2060172T3/en not_active Expired - Lifetime
- 1990-06-08 AT AT90908440T patent/ATE111507T1/en not_active IP Right Cessation
- 1990-06-08 US US07/623,970 patent/US5152883A/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
See references of WO9015121A1 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2597135A1 (en) * | 2011-11-24 | 2013-05-29 | IFP Energies nouvelles | Method for generating middle distillates from a conventional heavy feedstock including a step of selective hydrogenation of the HCO EX FCC cut |
FR2983208A1 (en) * | 2011-11-24 | 2013-05-31 | IFP Energies Nouvelles | PROCESS FOR PRODUCING MEDIUM DISTILLATE FROM A CONVENTIONAL HEAVY LOAD INCLUDING A SELECTIVE HYDROGENATION STEP FROM THE EXC FCC HCO CUT |
US8968554B2 (en) | 2011-11-24 | 2015-03-03 | IFP Energies Nouvelles | Process for the production of middle distillate from a conventional heavy feedstock including a step for selective hydrogenation of the ex FCC HCO cut |
Also Published As
Publication number | Publication date |
---|---|
ATE111507T1 (en) | 1994-09-15 |
DE69012526T2 (en) | 1995-03-30 |
US5152883A (en) | 1992-10-06 |
WO1990015121A1 (en) | 1990-12-13 |
ES2060172T3 (en) | 1994-11-16 |
EP0432235B1 (en) | 1994-09-14 |
JPH04500231A (en) | 1992-01-16 |
DE69012526D1 (en) | 1994-10-20 |
DK0432235T3 (en) | 1994-11-21 |
BE1004277A4 (en) | 1992-10-27 |
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