CA2087229A1 - Reduction de la teneur en benzene dans les essences - Google Patents
Reduction de la teneur en benzene dans les essencesInfo
- Publication number
- CA2087229A1 CA2087229A1 CA002087229A CA2087229A CA2087229A1 CA 2087229 A1 CA2087229 A1 CA 2087229A1 CA 002087229 A CA002087229 A CA 002087229A CA 2087229 A CA2087229 A CA 2087229A CA 2087229 A1 CA2087229 A1 CA 2087229A1
- Authority
- CA
- Canada
- Prior art keywords
- catalyst
- isomerization
- hydrogenation
- per
- platinum
- 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.)
- Abandoned
Links
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 title claims abstract description 63
- 238000000034 method Methods 0.000 claims abstract description 21
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 238000004821 distillation Methods 0.000 claims abstract description 6
- 238000006317 isomerization reaction Methods 0.000 claims description 29
- 239000003054 catalyst Substances 0.000 claims description 28
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 24
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 14
- 229910052697 platinum Inorganic materials 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 229910052763 palladium Inorganic materials 0.000 claims description 7
- 229910052680 mordenite Inorganic materials 0.000 claims description 6
- 239000000686 essence Substances 0.000 claims 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 16
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000010457 zeolite Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229910021536 Zeolite Inorganic materials 0.000 description 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 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 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000001833 catalytic reforming Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- VBEKGXAPCZTFJW-UHFFFAOYSA-N benzene;octane Chemical compound C1=CC=CC=C1.CCCCCCCC VBEKGXAPCZTFJW-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000005341 cation exchange Methods 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical class C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-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
- C10G69/08—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 reforming naphtha
-
- 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
-
- 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
- C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
- C10G65/02—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
- C10G65/04—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps
- C10G65/08—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps at least one step being a hydrogenation of the aromatic hydrocarbons
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR92/00.433 | 1992-01-13 | ||
FR9200433A FR2686096B1 (fr) | 1992-01-15 | 1992-01-15 | Reduction de la teneur en benzene dans les essences. |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2087229A1 true CA2087229A1 (fr) | 1993-07-14 |
Family
ID=9425702
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002087229A Abandoned CA2087229A1 (fr) | 1992-01-13 | 1993-01-13 | Reduction de la teneur en benzene dans les essences |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0552072B1 (ko) |
KR (1) | KR100242918B1 (ko) |
CA (1) | CA2087229A1 (ko) |
DE (1) | DE69321741T2 (ko) |
ES (1) | ES2125959T3 (ko) |
FR (1) | FR2686096B1 (ko) |
ID (1) | ID852B (ko) |
MY (1) | MY106926A (ko) |
TW (1) | TW237474B (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0953626A1 (de) * | 1998-04-27 | 1999-11-03 | FE Forschungs & Entwicklung GmbH | Verfahren zur Herstellung eines benzolarmen, hochoktanigen Kohlenwasserstoffgemischs |
WO2000069993A1 (en) * | 1999-05-13 | 2000-11-23 | Mobil Oil Corporation | Dual catalyst system |
EP2277980B1 (fr) | 2009-07-21 | 2018-08-08 | IFP Energies nouvelles | Procédé de réduction sélective de la teneur en benzène et en composés insatures legers de differentes coupes hydrocarbures |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA975384A (en) * | 1971-04-19 | 1975-09-30 | Graham K. Hilder | Isomerisation of paraffin hydrocarbons |
US5003118A (en) * | 1989-12-29 | 1991-03-26 | Uop | Isomerization of benzene-containing feedstocks |
-
1992
- 1992-01-15 FR FR9200433A patent/FR2686096B1/fr not_active Expired - Lifetime
- 1992-12-31 TW TW081110537A patent/TW237474B/zh active
-
1993
- 1993-01-07 EP EP93400023A patent/EP0552072B1/fr not_active Expired - Lifetime
- 1993-01-07 DE DE69321741T patent/DE69321741T2/de not_active Expired - Lifetime
- 1993-01-07 ES ES93400023T patent/ES2125959T3/es not_active Expired - Lifetime
- 1993-01-12 KR KR1019930000301A patent/KR100242918B1/ko not_active IP Right Cessation
- 1993-01-12 ID IDP532493A patent/ID852B/id unknown
- 1993-01-12 MY MYPI93000045A patent/MY106926A/en unknown
- 1993-01-13 CA CA002087229A patent/CA2087229A1/fr not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
DE69321741T2 (de) | 1999-03-18 |
EP0552072A1 (fr) | 1993-07-21 |
TW237474B (ko) | 1995-01-01 |
FR2686096A1 (fr) | 1993-07-16 |
KR930016527A (ko) | 1993-08-26 |
DE69321741D1 (de) | 1998-12-03 |
ID852B (id) | 1996-08-02 |
FR2686096B1 (fr) | 1994-04-29 |
KR100242918B1 (ko) | 2000-02-01 |
ES2125959T3 (es) | 1999-03-16 |
MY106926A (en) | 1995-08-30 |
EP0552072B1 (fr) | 1998-10-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0515256B1 (fr) | Procédé d'hydromérisation de paraffines issues du procédé Fischer-Tropsch à l'aide de catalyseurs à base de zéolithe H.Y | |
EP0242260B1 (fr) | Procédé de réformage catalytique | |
FR2720073A1 (fr) | Procédé d'hydrotraitement pour la production de supercarburant léger isomérisé et système de catalyseur d'hydroconversion. | |
FR2611739A1 (fr) | Procede d'activation d'un catalyseur d'isomerisation de paraffines normales | |
EP0789739A1 (fr) | Procede d'hydroisomerisation selective de paraffines longues lineaires et/ou peu ramifiees avec un catalyseur a base de tamis moleculaire | |
CA2194085C (fr) | Procede de reduction selective de la teneur en benzene et en composes insatures legers d'une coupe d'hydrocarbures | |
EP0661095B1 (fr) | Catalyseur pour la réduction de la teneur en benzène dans les essences | |
EP0552070B1 (fr) | Réduction de la teneur en benzène dans les essences | |
EP0661370B1 (fr) | Catalyseur pour la réduction de la teneur en benzène dans les essences | |
FR2548204A1 (fr) | Procede de transformation d'hydrocarbures | |
EP0196965B1 (fr) | Nouveau catalyseur d'isomérisation de coupes riches en paraffines normales | |
FR2676750A1 (fr) | Procede d'hydrocraquage de paraffines issue du procede fischer-tropsch a l'aide de catalyseurs a base de zeolithe h-y. | |
EP0552069B1 (fr) | Réduction de la teneur en benzène dans les essences par un procédé d'isomérisation | |
CA1334980C (fr) | Procede d'isomerisation du butene-1 en butenes-2 dans une coupe d'hydrocarbures en c _ contenant du butadiene et des composes sulfures | |
EP1417283B1 (fr) | Procede d'isomerisation d'une coupe c5-c8 mettant en oeuvre deux reacteurs en parallele | |
EP0440540B1 (fr) | Procédé d'isomérisation de paraffines normales en présence d'au moins un catalyseur à base d'une zéolithe oméga particulière | |
EP0552072B1 (fr) | Réduction de la teneur en benzène dans les essences | |
FR2694565A1 (fr) | Réduction de la teneur en benzène dans les essences. | |
FR2686094A1 (fr) | Production de base pour carburant exempt de benzene, presentant un indice d'octane eleve. | |
EP0922747B1 (fr) | Procédé d'isomérisation des coupes paraffiniques C5-C8 riches en paraffines à plus de sept atomes de carbone | |
FR2738243A1 (fr) | Procede d'hydroisomerisation de paraffines longues lineaires et/ou peu ramifiees avec un catalyseur a base de zeolithe nu-10 | |
FR2738244A1 (fr) | Procede d'hydroisomerisation selective de paraffines longues lineaires et/ou peu ramifiees avec un catalyseur a base de tamis moleculaire |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |