GB693237A - Hydrocarbon separation process - Google Patents
Hydrocarbon separation processInfo
- Publication number
- GB693237A GB693237A GB29998/50A GB2999850A GB693237A GB 693237 A GB693237 A GB 693237A GB 29998/50 A GB29998/50 A GB 29998/50A GB 2999850 A GB2999850 A GB 2999850A GB 693237 A GB693237 A GB 693237A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aromatic
- solvent
- primary separation
- subjected
- lean fraction
- 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
- C10G67/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
- C10G67/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
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 hydrocarbon mixture is subjected to a primary separation to yield an aromatic-rich and an aromatic-lean fraction, the aromatic-lean fraction is subjected to selective adsorption to remove substantially all aromatics, the solid adsorbent after use is regenerated by washing with the aromatic-lean fraction at elevated temperature and the effluent from the solid adsorbent during regeneration is recycled to the primary separation. Hydrocarbon mixtures mentioned include petroleum distillates, such as kerosene, and cracked and reformed naphthas. The aromatic-rich fraction obtained may constitute a toluene or xylene of high purity. The primary separation may be solvent extraction with liquid sulphur dioxide, furfural or nitrobenzene as the solvent, a "Duosol" extraction employing propane and phenol-cresol mixture as the solvent, an extractive distillation with a solvent such as phenol, or an azeotropic distillation using for example methyl ethyl ketone and water to form the azeotrope. Adsorbents mentioned are silica gel, alumina gel, silicaalumina gel and activated carbon or charcoal. In the examples, petroleum kerosene distillate is first solvent-extracted with liquid sulphur dioxide and then contacted with silica gel according to the above-described process.ALSO:A hydrocarbon mixture is subjected to a primary separation to yield an aromatic-rich and an aromatic-lean fraction, the aromatic-lean fraction is subjected to selective adsorption to remove substantially all aromatics, the solid adsorbent after use is regenerated by washing with the aromatic-lean fraction at elevated temperature and the effluent from the solid adsorbent during regeneration is recycled to the primary separation. Hydrocarbon mixtures mentioned are petroleum distillates, such as p kerosene, Diesel fuel and lubricating oil distillates, and cracked and reformed naphthas. Stocks suitable for the production of spray oils, cosmetic oils, medicinal oils and other white oils may be subjected to the process to produce substantially aromatic-free products which require no acid-treating step in order to meet commercial specifications. Where lubricating oils are treated the lubricating oil raffinate obtained from the primary separation may be diluted with a light hydrocarbon liquid before being subjected to selective adsorption. Suitable light hydrocarbons are low boiling paraffins such as pentane or isopentane or a light gasoline. The primary separation may be solvent extraction with liquid sulphur dioxide, furfural or nitrobenzene as the solvent, a "Duosol" extraction employing propane and phenolcresol mixture as the solvent, an extractive distillation with a solvent such as phenol, or an azeotropic distillation using for example methyl ethyl ketone and water to form the azeotrope. Adsorbents mentioned are silica gel, alumina gel, silica-alumina gel and activated carbon or charcoal. In the examples, petroleum kerosene distillate is first solvent-extracted with liquid sulphur dioxide and then contacted with silica gel according to the above-described process.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US693237XA | 1950-01-09 | 1950-01-09 | |
US1031703XA | 1950-01-09 | 1950-01-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB693237A true GB693237A (en) | 1953-06-24 |
Family
ID=26749924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB29998/50A Expired GB693237A (en) | 1950-01-09 | 1950-12-07 | Hydrocarbon separation process |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1031703A (en) |
GB (1) | GB693237A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2893944A (en) * | 1955-04-19 | 1959-07-07 | Standard Oil Co | Process for separation of gasoline fractions of different octane number by cyclic adsorption |
US2870230A (en) * | 1956-07-27 | 1959-01-20 | California Research Corp | Adsorption separation process |
-
1950
- 1950-12-07 GB GB29998/50A patent/GB693237A/en not_active Expired
- 1950-12-12 FR FR1031703D patent/FR1031703A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1031703A (en) | 1953-06-25 |
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