US2560330A - Method of refining kerosene with bauxite and sulfur dioxide - Google Patents
Method of refining kerosene with bauxite and sulfur dioxide Download PDFInfo
- Publication number
- US2560330A US2560330A US51105A US5110548A US2560330A US 2560330 A US2560330 A US 2560330A US 51105 A US51105 A US 51105A US 5110548 A US5110548 A US 5110548A US 2560330 A US2560330 A US 2560330A
- Authority
- US
- United States
- Prior art keywords
- kerosene
- sulphur
- bauxite
- range
- 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 - Lifetime
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
- 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
- C10G21/08—Inorganic compounds only
- C10G21/10—Sulfur dioxide
Definitions
- the present invention is concerned with an improved process for the production of high quality kerosenes.
- the invention is more particularly concerned with the production of kerosenes of low sulphur content, which kerosenes are derived from Near East crudes.
- kerosenes of relatively low sulphur content are produced by treating kerosene fractions in an initial stage with bauxite followed by contacting the kerosene fractions in a secondary stage with sulphur dioxide.
- hydrocarbon fractions By various procedures in order to reduce and remove sulphur compounds. For example, it is known to treat hydrocarbon fractions boiling in the kerosene boiling range with sulphuric acid in order to remove objectionable sulphur constituents. It is also known to treat hydrocarbon fractions boiling in the kerosene boiling range with doctor solution in order to convert the sulphur compounds into relatively innocuous disulfides. While these processes have been satisfactory for rteating these fractions .boiiing in the kerosene range secured from domestic crudes, they have not been entirely satisfactory for treating kerosene fractions secured from crudes having a relatively high sulphur content, particularly from' crudes from the Near East.
- crudes secured from the Near East, such as Kuwait, Iraq, Iran, and Arabia are of a particular nature, specifically with respect to the fraction boiling in the kerosene boiling range. These crudes have a relatively high sulphur content ranging from about 1% to as high as 7% by weight.
- the kerosene fractions boiling. in the range from about 300 F; to 580 F. secured from domestic crudes generally have a sulphur content, not in excess of about 0.2%.
- Kerosene fractions derived from Near East crudes have sulphur contents in the range of from 3% to .5%.
- the sulphur compounds are of two distinct varieties. These compounds seem to have alkyl mercaptans and thiophenic structures. In order to remove or reduce the concentration of the varied and complex sulphur constituents, various procedures have been-attempted.
- Sulfuric acid is not entirely satisfactory for the removal of these complex sulphur compounds nor will a solvent treat reduce them to the desired extent when using limited commercially feasible amounts ofsolvent.
- the present process which comprises a vapor phase bauxite trcatment, combined with an S02 extraction operation, functions satisfactorily to reduce the mercaptanic sulphur and to remove the thiophenic compounds.
- high sulphur kerosenes derived from Near East crudes are treated with bauxite at a temperature ranging from about 600 to 850 F. and at a pressure ranging from about 0 to 50 pounds per square inch absolute.
- Operating conditions are generally selected so that substantially no cracking of constituents other than the sulphur compounds results.
- the treating agent employed is a bauxite, preferably a nat urally occurring bauxite, which is preheated at a temperature within the range of about 600 F. to 1150 F. for a period sufficient to remove the water of hydration.
- it is preferred when treating kerosene fractions of the type under consideration to employ a temperature in the range from about 700 to 750 F. and to employ atmospheric pressure in the bauxite treating stage.
- the bauxite-treated stream is then condensed and treated with liquid sulphur dioxide.
- the sulphur dioxide stage is operated preferably at a temperature in the range of from about 20 to 40. F.
- the quantity of S02 employed may vary appreciably, but it is preferred to be with--. in the range from about 35% to 120% by volume. Although batch treatment may be employed, it is preferred that the S02 treatment comprises a countercurrent operation.
- the kerosene described above in one operation was bauxite-treated at a temperature of about 750 F. and at a pressure of about atmospheric.
- the kerosene product of this operation had the following specifications:
- Example II The feed kerosene employed in Example I in another operation was treatedwith sulphur dioxide employing 80% by volume of sulphur dioxide treat. The results of this operation were as fol- It is to be noted from the above data that the yield was relatively low, that the sulphur content of the kerosene was in excess of that considered satisfactory and that furthermore, the kerosene product did not pass the doctor test.
- Example III A kerosene similar to that employed in Example I was treated similarly as described with respect to Example II except that the quantity of sulphur dioxide employed was 120%. The results of this operation were as follows:
- Example IV A kerosene similar to that employed in Example I was treated as described with respect to Example II except that the quantity of sulphur It is to be observed that although the yield was relatively high, the sulphur content was excessive and the product did not pass the doctor test.
- Example V A kerosene similar to that employed in Example I was acid treated with 20 lbs. per barrel 4 using 98% sulfuric acid. The product was neutralized and rerun. The rerun product showed the following inspections:
- Example VI A kerosene similar to that utilized in Example I was treated in the vapor phase with bauxite at a temperature of 750 F. Atmospheric pressure was employed and the feed rate was 1/v./v./hr. The bauxite-treated kerosene was condensed and treated at a temperature of +l4 F. with 50% by volume of sulphur dioxide. The results of this operation were as follows:
- the present invention is adapted particularly for the treatment of hydrocarbon fractions boiling in the kerosene boiling range. It is especially suitable for treating kerosenes derived from crudes having a sulphur content in the range from 1-'7% and wherein the sulphur content of the kerosene product is in the range from about .2 to 5% and higher and particularly when the sulphur content of the kerosene is in the range from .3 to .6%.
- the boiling range of the kerosene fractions is in the general range from about 300 F. to 600 F. and
- the amount of sulphur dioxide employed in the second stage may vary appreciably, but it is preferred that approximately 40-60% of sulphur dioxide be employed per volume of kerosene, and that the temperature be in the range from about 0 F. to 20 F. However, if it is desired that the final product have a sulphur content below about .03% the amount of sulphur dioxide by volume employed will range from about -120%.
- the bauxite treatment in the initial stage is conducted at temperature and pressure conditions wherein practically I no cracking of the kerosene hydrocarbons occur. It is preferred that the kerosene fraction be treated at a temperature in the range from 600-850 F. and preferably in the range from 700-750" F. It is also preferred that the pressure be about atmospheric although pressures up to about 50 lbs. may be used.
- Process for the production of a kerosene of relatively low sulfur content which comprises treating in the vapor phase at a temperatur between 600 and 850 F. and at a pressure between 0 and 50 lbs. per square inch a hydrocarbon fraction boiling in the kerosene boiling range in an initial stage with bauxite, withdrawing a bauxite-treated fraction, condensin the same, and contacting it in the liquid phase in a secondary stage with liquid sulfur dioxide and recovering a kerosene fraction of a relatively low sulfur content from said secondary stage.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (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 July 10, 1951 METHOD or REFINING KERosENii WITH BAUXITE AND SULFUR DIOXIDE Richard O.Brandon, Elizabeth, N. 3., assignor to Standard Oil Development Company, a come-- ration of Delaware N Drawing. Application September 24, 1948, Serial No. 51,105
4 Claims.
The present invention is concerned with an improved process for the production of high quality kerosenes. The invention is more particularly concerned with the production of kerosenes of low sulphur content, which kerosenes are derived from Near East crudes. In accordance with the present invention, kerosenes of relatively low sulphur content are produced by treating kerosene fractions in an initial stage with bauxite followed by contacting the kerosene fractions in a secondary stage with sulphur dioxide.
It is wellknown in the art to treathydrocarbon fractionsby various procedures in order to reduce and remove sulphur compounds. For example, it is known to treat hydrocarbon fractions boiling in the kerosene boiling range with sulphuric acid in order to remove objectionable sulphur constituents. It is also known to treat hydrocarbon fractions boiling in the kerosene boiling range with doctor solution in order to convert the sulphur compounds into relatively innocuous disulfides. While these processes have been satisfactory for rteating these fractions .boiiing in the kerosene range secured from domestic crudes, they have not been entirely satisfactory for treating kerosene fractions secured from crudes having a relatively high sulphur content, particularly from' crudes from the Near East.
For example, crudes secured from the Near East, such as Kuwait, Iraq, Iran, and Arabia are of a particular nature, specifically with respect to the fraction boiling in the kerosene boiling range. These crudes have a relatively high sulphur content ranging from about 1% to as high as 7% by weight. On the other hand, the kerosene fractions boiling. in the range from about 300 F; to 580 F. secured from domestic crudes generally have a sulphur content, not in excess of about 0.2%. Also, due tothe difficulty and expense of reducingthe sulphur in a kerosene derived from high sulphur domestic sources, the general practice is to produce kerosenes from relatively sweet crudes which kerosene fractions have sulphur contents of about 04%.] v I Kerosene fractions derived from Near East crudes have sulphur contents in the range of from 3% to .5%. Furthermore, the sulphur compounds are of two distinct varieties. These compounds seem to have alkyl mercaptans and thiophenic structures. In order to remove or reduce the concentration of the varied and complex sulphur constituents, various procedures have been-attempted. Sulfuric acid is not entirely satisfactory for the removal of these complex sulphur compounds nor will a solvent treat reduce them to the desired extent when using limited commercially feasible amounts ofsolvent. The present process which comprises a vapor phase bauxite trcatment, combined with an S02 extraction operation, functions satisfactorily to reduce the mercaptanic sulphur and to remove the thiophenic compounds.
In accordance with the process of the present invention, high sulphur kerosenes derived from Near East crudes are treated with bauxite at a temperature ranging from about 600 to 850 F. and at a pressure ranging from about 0 to 50 pounds per square inch absolute. Operating conditions are generally selected so that substantially no cracking of constituents other than the sulphur compounds results. The treating agent employed is a bauxite, preferably a nat urally occurring bauxite, which is preheated at a temperature within the range of about 600 F. to 1150 F. for a period sufficient to remove the water of hydration. In general, it is preferred when treating kerosene fractions of the type under consideration, to employ a temperature in the range from about 700 to 750 F. and to employ atmospheric pressure in the bauxite treating stage.
The bauxite-treated stream is then condensed and treated with liquid sulphur dioxide. The sulphur dioxide stage is operated preferably at a temperature in the range of from about 20 to 40. F. The quantity of S02 employed may vary appreciably, but it is preferred to be with--. in the range from about 35% to 120% by volume. Although batch treatment may be employed, it is preferred that the S02 treatment comprises a countercurrent operation.
The present invention may be more fullyjunderstood by the following examples illustrating the same:
' Example I Sulphur, wt. per cent 0.363 Mercaptan sulphur, mg./ m1 19 Doctor test 1 DNP 1 Federal Specification Test Method 520.31.
- The kerosene described above in one operation was bauxite-treated at a temperature of about 750 F. and at a pressure of about atmospheric. The kerosene product of this operation had the following specifications:
Sulphur, wt. per cent 0.202 Mercaptan sulphur, mg./ 100 ml Nil Doctor test Pass It is to be noted that the fraction passed the doctor test, but that the sulphur content was relatively high and unsatisfactory. In order to have a satisfactory kerosene product, it is essential that the sulphur content be below 0.05%.
Example II The feed kerosene employed in Example I in another operation was treatedwith sulphur dioxide employing 80% by volume of sulphur dioxide treat. The results of this operation were as fol- It is to be noted from the above data that the yield was relatively low, that the sulphur content of the kerosene was in excess of that considered satisfactory and that furthermore, the kerosene product did not pass the doctor test.
Example III A kerosene similar to that employed in Example I was treated similarly as described with respect to Example II except that the quantity of sulphur dioxide employed was 120%. The results of this operation were as follows:
Yields, vol. per cent:
Product 75 Extract Rafilnate inspections:
Sulphur, wt. per cent 0.044 Mercaptan sulphur, mg./100 ml. '7 Doctor test DNP It is to be noted that the sulphur content of the kerosene was below .05% but that the finished product did not pass the doctor test. This failure to pass the doctor indicates the presence of mercaptan sulphur which is very undesirable in the finished product.
Example IV A kerosene similar to that employed in Example I was treated as described with respect to Example II except that the quantity of sulphur It is to be observed that although the yield was relatively high, the sulphur content was excessive and the product did not pass the doctor test.
Example V A kerosene similar to that employed in Example I was acid treated with 20 lbs. per barrel 4 using 98% sulfuric acid. The product was neutralized and rerun. The rerun product showed the following inspections:
Sulphur, wt. per cent 0.163 Mercaptan sulphur, mg./ 100 ml 1 Doctor test DNP It is evident that this operation did not produce a satisfactory kerosene.
Example VI A kerosene similar to that utilized in Example I was treated in the vapor phase with bauxite at a temperature of 750 F. Atmospheric pressure was employed and the feed rate was 1/v./v./hr. The bauxite-treated kerosene was condensed and treated at a temperature of +l4 F. with 50% by volume of sulphur dioxide. The results of this operation were as follows:
Yield, vol. per cent:
Yield 83 Extract 1'1 Raffinate inspections:
Sulphur, wt. per cent 0.043 Mercaptan sulphur, mg./ 100 ml. Nil Doctor test Pass It is to be noted that the sulphur content was below 0.5%, that the product passed the doctor test and that the yield was high.
As described heretofore, the present invention is adapted particularly for the treatment of hydrocarbon fractions boiling in the kerosene boiling range. It is especially suitable for treating kerosenes derived from crudes having a sulphur content in the range from 1-'7% and wherein the sulphur content of the kerosene product is in the range from about .2 to 5% and higher and particularly when the sulphur content of the kerosene is in the range from .3 to .6%. The boiling range of the kerosene fractions is in the general range from about 300 F. to 600 F. and
preferably in the range from about 350-500 F. The amount of sulphur dioxide employed in the second stage may vary appreciably, but it is preferred that approximately 40-60% of sulphur dioxide be employed per volume of kerosene, and that the temperature be in the range from about 0 F. to 20 F. However, if it is desired that the final product have a sulphur content below about .03% the amount of sulphur dioxide by volume employed will range from about -120%. The bauxite treatment in the initial stage is conducted at temperature and pressure conditions wherein practically I no cracking of the kerosene hydrocarbons occur. It is preferred that the kerosene fraction be treated at a temperature in the range from 600-850 F. and preferably in the range from 700-750" F. It is also preferred that the pressure be about atmospheric although pressures up to about 50 lbs. may be used.
Having described the invention, it is claimed:
1. Process for the production of a kerosene of relatively low sulfur content which comprises treating in the vapor phase at a temperatur between 600 and 850 F. and at a pressure between 0 and 50 lbs. per square inch a hydrocarbon fraction boiling in the kerosene boiling range in an initial stage with bauxite, withdrawing a bauxite-treated fraction, condensin the same, and contacting it in the liquid phase in a secondary stage with liquid sulfur dioxide and recovering a kerosene fraction of a relatively low sulfur content from said secondary stage.
2. Process for the production of a kerosene fraction boiling in the range between 300 and 600 F. from a crude oil containing in excess of about 1.0% sulfur which comprises segregating from said crude oil a kerosene fraction having a sulfur content above about .2% passing said kerosene fraction at a temperature between 700 and 750 F. and atmospheric pressure over bauxite, then treatin the bauxite-treated kerosene fraction in the liquid phase with liquid sulfur dioxide whereby a kerosene product having a sulfur content below 0.5% and which is substantially completely free from mercaptan sulfur is secured.
3. Process as defined by claim 2 wherein the sulphur content of the feed kerosene fraction is above about .3% and wherein said kerosene is contacted with from about 40-80% of sulphur dioxide by volume, and whereby a kerosene 6 product having a sulphur content below about .05'% is secured.
4. A process as defined by claim 2 wherein said feed kerosene has a sulphur content above about .3%, wherein said kerosene fraction is treated with from about 80-120% by volume of sulphur dioxide and whereby a kerosene product having a sulphur content below about .03% is secured.
RICHARD C. BRANDON.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS -Number Name Date 1,746,641 Ford Feb. 11, 1930 1,947,868 Morrell et a1. Feb. 20, 1934 20 2,391,091' Hewlett et a1. Dec. 18, 1945
Claims (1)
1. PROCESS FOR THE PRODUCTION OF A KEROSENE OF RELATIVELY LOW SULFUR CONTENT WHICH COMPRISES TREATING IN THE VAPOR PHASE AT A TEMPERATURE BETWEEN 600 AND 850* F. AND AT A PRESSURE BETWEEN 0 AND 50 LBS. PER SQUARE INCH A HYDROCARBON FRACTION BOILING IN THE KEROSENE BOILING RANGE IN AN INITIAL STAGE WITH BAUXITE, WITHDRAWING A BAUXITE-TREATED FRACTION, CONDENSING THE SAME, AND CONTACTING IT IN THE LIQUID PHASE IN A SECONDARY STAGE WITH LIQUID SULFUR DIOXIDE AND RECOVERING A KEROSENE FRACTION OF A RELATIVELY LOW SULFUR CONTENT FROM SAID SECONDARY STAGE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51105A US2560330A (en) | 1948-09-24 | 1948-09-24 | Method of refining kerosene with bauxite and sulfur dioxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51105A US2560330A (en) | 1948-09-24 | 1948-09-24 | Method of refining kerosene with bauxite and sulfur dioxide |
Publications (1)
Publication Number | Publication Date |
---|---|
US2560330A true US2560330A (en) | 1951-07-10 |
Family
ID=21969374
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US51105A Expired - Lifetime US2560330A (en) | 1948-09-24 | 1948-09-24 | Method of refining kerosene with bauxite and sulfur dioxide |
Country Status (1)
Country | Link |
---|---|
US (1) | US2560330A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2651594A (en) * | 1949-05-26 | 1953-09-08 | Standard Oil Dev Co | Kerosene finishing process |
US2697063A (en) * | 1952-04-24 | 1954-12-14 | Sinclair Refining Co | Desulfurizing petroleum distillate fuels with clay in the first stage and liquid sulfur dioxide in the second stage |
US2739102A (en) * | 1953-07-17 | 1956-03-20 | Standard Oil Co | Hydrocarbon desulfurization process by reacting the sulfur in the hydrocarbon with an olefin and a catalyst, then extracting the hydrocarbon with so2 and bf3 |
US2744855A (en) * | 1953-07-09 | 1956-05-08 | Standard Oil Co | Desulfurization process using alkali followed by extraction with liquid sulfur dioxide and a promoter |
US2755227A (en) * | 1954-03-22 | 1956-07-17 | Pure Oil Co | Removing corrosive sulfur from naphtha with anhydrous copper sulfate |
US2769762A (en) * | 1953-08-31 | 1956-11-06 | Pure Oil Co | Production of naphthas of improved characteristics by treating with bauxite |
US2769760A (en) * | 1953-09-11 | 1956-11-06 | Pure Oil Co | Production of sweet naphthas from hydrocarbon mixtures by hydrofining the hydrocarbon mixture followed by contacting the hydrocarbon product with a composition containing cobalt and molybdenum |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1746641A (en) * | 1927-08-06 | 1930-02-11 | Westinghouse Electric & Mfg Co | Purification of used insulating oils |
US1947868A (en) * | 1931-02-16 | 1934-02-20 | Universal Oil Prod Co | Treatment of hydrocarbon oils |
US2391091A (en) * | 1939-12-20 | 1945-12-18 | Standard Oil Dev Co | Refining petroleum oils |
-
1948
- 1948-09-24 US US51105A patent/US2560330A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1746641A (en) * | 1927-08-06 | 1930-02-11 | Westinghouse Electric & Mfg Co | Purification of used insulating oils |
US1947868A (en) * | 1931-02-16 | 1934-02-20 | Universal Oil Prod Co | Treatment of hydrocarbon oils |
US2391091A (en) * | 1939-12-20 | 1945-12-18 | Standard Oil Dev Co | Refining petroleum oils |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2651594A (en) * | 1949-05-26 | 1953-09-08 | Standard Oil Dev Co | Kerosene finishing process |
US2697063A (en) * | 1952-04-24 | 1954-12-14 | Sinclair Refining Co | Desulfurizing petroleum distillate fuels with clay in the first stage and liquid sulfur dioxide in the second stage |
US2744855A (en) * | 1953-07-09 | 1956-05-08 | Standard Oil Co | Desulfurization process using alkali followed by extraction with liquid sulfur dioxide and a promoter |
US2739102A (en) * | 1953-07-17 | 1956-03-20 | Standard Oil Co | Hydrocarbon desulfurization process by reacting the sulfur in the hydrocarbon with an olefin and a catalyst, then extracting the hydrocarbon with so2 and bf3 |
US2769762A (en) * | 1953-08-31 | 1956-11-06 | Pure Oil Co | Production of naphthas of improved characteristics by treating with bauxite |
US2769760A (en) * | 1953-09-11 | 1956-11-06 | Pure Oil Co | Production of sweet naphthas from hydrocarbon mixtures by hydrofining the hydrocarbon mixture followed by contacting the hydrocarbon product with a composition containing cobalt and molybdenum |
US2755227A (en) * | 1954-03-22 | 1956-07-17 | Pure Oil Co | Removing corrosive sulfur from naphtha with anhydrous copper sulfate |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2560330A (en) | Method of refining kerosene with bauxite and sulfur dioxide | |
US3354081A (en) | Process for desulfurization employing k2s | |
US1965828A (en) | Nitrogen base and method of making same | |
US1998849A (en) | Process for desulphurizing mercaptan-containing petroleum oil | |
US2273104A (en) | Refining mineral oils | |
US2973316A (en) | Process for preventing corrosion in ferrous systems | |
US1871694A (en) | Process for producing aromatic hydrocarbons | |
US2546345A (en) | Dethiolizing hydrocarbons | |
US1936210A (en) | Process of treating cracked petroleum distillates | |
US3049414A (en) | Color-stable gasoline | |
US2537620A (en) | Process for desulfurizing petroleum oils | |
US2204903A (en) | Process for desulphurizing mineral oils | |
US2578602A (en) | Dethiolizing hydrocarbons and other organic liquids | |
US2393476A (en) | Sweetening of gasoline | |
US2905638A (en) | Removal of sulfur dioxide from oils | |
US2051612A (en) | Method of treating oils | |
US1961204A (en) | Process of kefining a benzenoid | |
US2855445A (en) | Purification of normal heptane by treating with alkali polysulfide followed by a copper chloride treatment | |
US2009554A (en) | Process of producing pure mercaptans | |
US1971172A (en) | Treatment of hydrocarbon oils | |
US2948674A (en) | Low odor solvents | |
US2249276A (en) | Treatment of cracked hydrocarbon distillates | |
US2218610A (en) | Refining process | |
US1973901A (en) | Process of refining hydrocarbon oils | |
US2301281A (en) | Refining mineral oil |