US2000690A - Solvent refining of hydrocarbon oil - Google Patents
Solvent refining of hydrocarbon oil Download PDFInfo
- Publication number
- US2000690A US2000690A US696540A US69654033A US2000690A US 2000690 A US2000690 A US 2000690A US 696540 A US696540 A US 696540A US 69654033 A US69654033 A US 69654033A US 2000690 A US2000690 A US 2000690A
- Authority
- US
- United States
- Prior art keywords
- oil
- solvent
- hydrocarbon oil
- solvent refining
- constituents
- 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 - Lifetime
Links
- 239000002904 solvent Substances 0.000 title description 18
- 239000004215 Carbon black (E152) Substances 0.000 title description 3
- 229930195733 hydrocarbon Natural products 0.000 title description 3
- 150000002430 hydrocarbons Chemical class 0.000 title description 3
- 238000007670 refining Methods 0.000 title description 3
- 239000003921 oil Substances 0.000 description 14
- 239000000470 constituent Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000010687 lubricating oil Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 5
- 238000000605 extraction Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CRLNTRZMHKNJSR-UHFFFAOYSA-N furan-2-yl(phenyl)methanone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CO1 CRLNTRZMHKNJSR-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000005251 aryl acyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- C10G21/06—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents characterised by the solvent used
- C10G21/12—Organic compounds only
- C10G21/16—Oxygen-containing compounds
Definitions
- the foregoing solvent liquids are suitable for extracting undesired constituents from mineral oils, and particularly from lubricating oil fractions.
- Lubricating oils such as produced from midcontinent crude, are ordinarily composed of relatively paraffinic constituents, and also relatively non-paraffinic constituents,including naphthenic, aromatic, and unsaturated hydrocarbon bodies.
- the solvent of my invention is adapted to extract these relatively non-parafiinic bodies from the oil for the production of lubricating oil fractions which are of relatively high parafiinic character, and therefore of relatively higher viscosity index than the untreated oil.
- one part of the oil is mixed with about two parts of solvent liquid, and this mixture is then subjected to agitation and heating in order to efieot solution of the undesired constituents of the oil in the solvent.
- the extent to which the oil is soluble in the solvent will depend upon the nature of the oil as well as upon the condition of temperature and pressure employed. The conditions of temperature and pressure, as well as the ratio of solvent to oil, may be varied for the purpose of effecting the particular degree of extraction desired. The temperatures employed, for example, may range from about 0 F. to 200 F. or thereabouts.
- the mixture Upon settling, the mixture separates into two layers, one of which comprises the constituents which it is desired to extract from the oil dissolved in the bulk of the solvent liquid, while the other layer comprises the undissolved and relatively other sources.
- the two layers are then separately withdrawn, and the solvent liquid recovered therefrom. If desired, the separated layers may be subjected to treatment with additional quantities of the solvent for the purpose of obtaining a series of fractions of diiferingcharacteristics.
- one volume of dewaxed mid-continent distillate oil was mixed with two volumes of benzoylfuran and the mixture heated to about 176? F. At this temperature and while at atmospheric pressure, there was a separation of the mixture into a rafiinate phase and an extract phase, the raffinate phase containing about 70% of the oil while the extract phase contained about 30%.
- a modifying solvent liquid such as benzol or a light petroleum naphtha
- a suitable modifying solvent for this purpose may comprise propane or butane.
- the lubricating oil distillate may be subjected to the foregoing extraction treatment, either before or after dewaxing, or subsequent to treat ment with other solvents or chemicals.
- the invention is not necessarily limited to the treatment of lubricating oil fractions, since the solvent may be adapted to the refining and purification of various hydrocarbon or mineral oil fractions, including naphtha, cracked naphtha, kerosene, etc., as well as residual or distillate fractions, or products derived from petroleum or
- the acyl derivatives of furan in the foregoing specification and inthe appended the oil with a solvent selected from the group desired relatively non-parafiinic constituents therefrom, which comprises extractively treating the oil with an aryl acyl derivative of iuran of the character of benzoyl furan whereby the undesired constituents are separated from the oil as an extract soluble in the solvent liquid.
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)
Description
Patented May 7, 1935 UNITED STATES PATENT OFFICE I 1 7 2,000,690 SOLVENT REFINING or HYDROCARBON on.
Louis A. Clarke, Fishkill, N. Y., assignor to The Texas Company, New York, N. Y., a corporation of Delaware No Drawing. Application November 3, 1933,
Serial No. 696,540
2 Claims.
The foregoing solvent liquids are suitable for extracting undesired constituents from mineral oils, and particularly from lubricating oil fractions.
Lubricating oils, such as produced from midcontinent crude, are ordinarily composed of relatively paraffinic constituents, and also relatively non-paraffinic constituents,including naphthenic, aromatic, and unsaturated hydrocarbon bodies. The solvent of my invention is adapted to extract these relatively non-parafiinic bodies from the oil for the production of lubricating oil fractions which are of relatively high parafiinic character, and therefore of relatively higher viscosity index than the untreated oil.
In the application of my invention to the treatment of mineral oils for the production of lubricating oil, one part of the oil is mixed with about two parts of solvent liquid, and this mixture is then subjected to agitation and heating in order to efieot solution of the undesired constituents of the oil in the solvent. The extent to which the oil is soluble in the solvent will depend upon the nature of the oil as well as upon the condition of temperature and pressure employed. The conditions of temperature and pressure, as well as the ratio of solvent to oil, may be varied for the purpose of effecting the particular degree of extraction desired. The temperatures employed, for example, may range from about 0 F. to 200 F. or thereabouts.
Upon settling, the mixture separates into two layers, one of which comprises the constituents which it is desired to extract from the oil dissolved in the bulk of the solvent liquid, while the other layer comprises the undissolved and relatively other sources.
paraflinic oil in admixture with a relatively small amount of solvent. V
The two layers are then separately withdrawn, and the solvent liquid recovered therefrom. If desired, the separated layers may be subjected to treatment with additional quantities of the solvent for the purpose of obtaining a series of fractions of diiferingcharacteristics.
By way of a specific example, one volume of dewaxed mid-continent distillate oil was mixed with two volumes of benzoylfuran and the mixture heated to about 176? F. At this temperature and while at atmospheric pressure, there was a separation of the mixture into a rafiinate phase and an extract phase, the raffinate phase containing about 70% of the oil while the extract phase contained about 30%.
In some instances, it maybe of advantage to carry out the extraction in the presence of a modifying solvent liquid, such as benzol or a light petroleum naphtha, for the purpose of facilitating the extraction and further controlling the extent thereof. A suitable modifying solvent for this purpose may comprise propane or butane.
The lubricating oil distillate may be subjected to the foregoing extraction treatment, either before or after dewaxing, or subsequent to treat ment with other solvents or chemicals. The invention is not necessarily limited to the treatment of lubricating oil fractions, since the solvent may be adapted to the refining and purification of various hydrocarbon or mineral oil fractions, including naphtha, cracked naphtha, kerosene, etc., as well as residual or distillate fractions, or products derived from petroleum or By reference to the acyl derivatives of furan in the foregoing specification and inthe appended the oil with a solvent selected from the group desired relatively non-parafiinic constituents therefrom, which comprises extractively treating the oil with an aryl acyl derivative of iuran of the character of benzoyl furan whereby the undesired constituents are separated from the oil as an extract soluble in the solvent liquid.
LOUIS A.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US696540A US2000690A (en) | 1933-11-03 | 1933-11-03 | Solvent refining of hydrocarbon oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US696540A US2000690A (en) | 1933-11-03 | 1933-11-03 | Solvent refining of hydrocarbon oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2000690A true US2000690A (en) | 1935-05-07 |
Family
ID=24797481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US696540A Expired - Lifetime US2000690A (en) | 1933-11-03 | 1933-11-03 | Solvent refining of hydrocarbon oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2000690A (en) |
-
1933
- 1933-11-03 US US696540A patent/US2000690A/en not_active Expired - Lifetime
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