GB824635A - Process for improving kerosenes and diesel fuels - Google Patents
Process for improving kerosenes and diesel fuelsInfo
- Publication number
- GB824635A GB824635A GB2184458A GB2184458A GB824635A GB 824635 A GB824635 A GB 824635A GB 2184458 A GB2184458 A GB 2184458A GB 2184458 A GB2184458 A GB 2184458A GB 824635 A GB824635 A GB 824635A
- Authority
- GB
- United Kingdom
- Prior art keywords
- stage
- stages
- nickel
- cobalt molybdate
- over
- 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.)
- Expired
Links
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
- 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
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
A process for upgrading petroleum fractions containing aromatic and sulphur compounds and boiling in the range 300 DEG to 650 DEG F. comprises first desulphurizing the fractions to not more than 20 p.p.m. of sulphur and thereafter hydrogenating them over a nickel catalyst at hydrogen rates in excess of 2000 SCF/Bbl. The first stage desulphurization is preferably effected by hydrofining over cobalt molybdate on alumina at 600 DEG to 800 DEG F., 200 to 800 p.s.i.g. and 1 V/hr./V. In the second hydrogenation stage the nickel is preferably supported on kieselguhr, the preferred conditions being 500-550 DEG F., 200-800 p.s.i.g., 1-5 V/hr/V and 2000-10,000 SCF/B. Recycle hydrogen may be used in both stages, H2S being scrubbed out before contact with the Ni catalyst, but preferably retained for the cobalt molybdate hydrofining stage. In an example a 300-650 DEG F. diesel fuel fraction is heated to 725 DEG F. and passed downwardly first over cobalt molybdate and then nickel in countercurrent to H2S free hydrogen which is not scrubbed free from the H2S formed in the Ni stage between stages. The oil is cooled to 500-550 DEG F. by heat exchange with the cold feed between the stages. The process is particularly applicable to the saturation of fractions containing 10-50% of atomatics and having a naphthalene ring content below 30%.ALSO:A process for upgrading petroleum fractions containing aromatic and sulphur compounds and boiling in the range 300 DEG to 650 DEG F., comprises first desulphurizing the fractions to not more than 20 p.p.m. of sulphur and thereafter hydrogenating them over a nickel catalyst at hydrogen rates in excess of 2000 SCF/Bbl. The first stage desulphurization is preferably effected by hydrofining over cobalt molybdate/alumina at 600 DEG to 800 DEG F., 200 to 800 p.s.i.g., and 1 v./H2/v. In the second hydrogenation stage the nickel is preferably supported on kieselguhr, the preferred conditions being 500-550 DEG F., 200-800 p.s.i.g., 1-5 v./H2/v. and 2000-10,000 SCF/B. Recycle hydrogen may be used in both stages, H2S being scrubbed out before contact with the Ni catalyst, but preferably retained for the cobalt molybdate hydrofining stage. In an example a 300-650 DEG F. diesel fuel fraction is heated to 725 DEG F. and passed downwardly first over cobalt molybdate and then nickel in countercurrent to H2S-free hydrogen which is not scrubbed free from the H2S formed in the Ni stage between stages. The oil is cooled to 500-550 DEG F. by heat exchange with the cold feed between the stages. The process is particularly applicable to the saturation of fractions containing 10-50% of aromatics and having a naphthalene ring content below 30%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2184458A GB824635A (en) | 1958-07-08 | 1958-07-08 | Process for improving kerosenes and diesel fuels |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2184458A GB824635A (en) | 1958-07-08 | 1958-07-08 | Process for improving kerosenes and diesel fuels |
Publications (1)
Publication Number | Publication Date |
---|---|
GB824635A true GB824635A (en) | 1959-12-02 |
Family
ID=10169761
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2184458A Expired GB824635A (en) | 1958-07-08 | 1958-07-08 | Process for improving kerosenes and diesel fuels |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB824635A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001207177A (en) * | 2000-01-25 | 2001-07-31 | Haldor Topsoe As | Method for reducing content of sulfur compound and polycyclic aromatic hydrocarbon in hydrocarbon feed |
JP2006104271A (en) * | 2004-10-01 | 2006-04-20 | Nippon Oil Corp | Method for producing hydrofined gas oil, hydrofined gas oil, and gas oil composition |
-
1958
- 1958-07-08 GB GB2184458A patent/GB824635A/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001207177A (en) * | 2000-01-25 | 2001-07-31 | Haldor Topsoe As | Method for reducing content of sulfur compound and polycyclic aromatic hydrocarbon in hydrocarbon feed |
EP1120453A2 (en) * | 2000-01-25 | 2001-08-01 | Haldor Topsoe A/S | Process for reduction of content of sulphur compounds and poly-aromatic hydrocarbons in distillate fuels |
EP1120454A2 (en) * | 2000-01-25 | 2001-08-01 | Haldor Topsoe A/S | Process for reducting content of sulphur compounds and poly-aromatic hydrocarbons in hydrocarbon feed |
EP1120454A3 (en) * | 2000-01-25 | 2002-01-30 | Haldor Topsoe A/S | Process for reducting content of sulphur compounds and poly-aromatic hydrocarbons in hydrocarbon feed |
EP1120453A3 (en) * | 2000-01-25 | 2002-01-30 | Haldor Topsoe A/S | Process for reduction of content of sulphur compounds and poly-aromatic hydrocarbons in distillate fuels |
JP2006104271A (en) * | 2004-10-01 | 2006-04-20 | Nippon Oil Corp | Method for producing hydrofined gas oil, hydrofined gas oil, and gas oil composition |
EP1818385A1 (en) * | 2004-10-01 | 2007-08-15 | Nippon Oil Corporation | Process for producing hydrorefined gas oil, hydrorefind gas oil, and gas oil composition |
EP1818385A4 (en) * | 2004-10-01 | 2008-12-17 | Nippon Oil Corp | Process for producing hydrorefined gas oil, hydrorefind gas oil, and gas oil composition |
JP4643966B2 (en) * | 2004-10-01 | 2011-03-02 | Jx日鉱日石エネルギー株式会社 | Process for producing hydrorefined gas oil, hydrorefined gas oil and gas oil composition |
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