US1938672A - Desulphurizing hydrocarbon oils - Google Patents
Desulphurizing hydrocarbon oils Download PDFInfo
- Publication number
- US1938672A US1938672A US376290A US37629029A US1938672A US 1938672 A US1938672 A US 1938672A US 376290 A US376290 A US 376290A US 37629029 A US37629029 A US 37629029A US 1938672 A US1938672 A US 1938672A
- Authority
- US
- United States
- Prior art keywords
- sulphur
- distillate
- sodium
- alkali metal
- metal
- 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
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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
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/02—Non-metals
-
- 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
- C10G19/00—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
-
- 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
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/04—Metals, or metals deposited on a carrier
Definitions
- the present invention relates to improvements in desulphurizing hydrocarbon oils, and more particularly the lower boiling point distillates such as distillates in the gasoline and kerosene boiling point range. It has been found particularly suited for use in connection with cracked distillates from high sulphur oil, such as Lander and Winkler oils which distillates contain sulphur bodies of a highly refractory type and which are diflicult to remove.
- the alkali metals such as sodium and potassium are preferably employed to effect the desulphurizing.
- the metal used may be employed in lumps (massive) in operating in accordance with the present invention, and metals fusible at the temperature of operation are then preferred.
- the active metal is employed in a proportion equal to or substantially exceeding the atomic equivalent of the amount of sulphur present.
- the atomic proportion of the metal to the sulphur should exceed 1 to 1, and proportions in excess of 3 to 1 are preferred.
- the distillate and the active metal are heated together to a temperature of at least 400 F. and preferably not exceeding 650 F. In general a temperature of at least 500 F. is preferred.
- the operation is conducted under pressure, generally in excess of 150 lbs. per sq. in. and preferably from 200 'to 300 lbs. per sq. in. Higher pressures are employed when lower boiling constituents are present. Under these temperature and pressure conditions the distillate is of course substantially in the liquid state and the alkali metal is in the molten condition.
- a gasoline derived by a vapor phase cracking operation from a high sulphur crude oil was treated with lump sodium, the atomic ratio of sodium to sulphur being 4 to 1 at a temperature of 575 F. and a pressure of 290 lbs. per sq. in. for three hours with vigorous agitation, the percentage of sulphur being reduced from an initial value of 0.182 to 0.087.
- the 225 to 420 F. cut of another distillate derived by an ordinary cracking process from a sulphur-containing crude was treated in the presence of an inert substantially sulphur-free heavy oil having an initial boiling point above 600 F. with sodium in an atomic ratio to the sulphur of 4.65 to 1 at a temperature of 560 F. and a pressure of 175 lbs., the sulphur content being reduced from 0.473% to about 0.1%. It is thus apparent that the admixture of a heavy oil which, has an initial boiling point substantially above the end point of the distillate oil and is therefore readily separable from the low boiling distillate, improves the effectiveness of the action of the active metal.
- alkali metals such as lithium, potassium and the like are similarly efiective.
- sodium or other active alkali metal When sodium or other active alkali metal is employed in lump form, it may be screened or otherwise separated out of the treated oil and reused for the treatment of fresh sulphurcontaining distillate, suflicient additional fresh metal being supplied to bring the atomic ratio of metal to sulphur to the desired figure.
- suflicient additional fresh metal being supplied to bring the atomic ratio of metal to sulphur to the desired figure.
- an excess over such calculated amount should be supplied for replenishment or the amount of sodium present will be insufficient to effect the desired desulphurization.
- the sodium or other active metal may be reused as long as the amount present is sufficient for effective reaction, additional metal being added as required to maintain effectiveness.
- the operation may be conducted in an atmosphere of a gas inert to the oil and alkali metal under the conditions of the process, such as hydrogen or nitrogen. This serves to increase the effectiveness of sulphur removal with a given ratio of metal to sulphur.
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 Dec. 12, 1933 DESULPHURIZING nYnRocAaBoN or s Robert F. Ruthruff, Hammond, Ind, assignor to Standard'Oil Company, Whiting, Ind., a corporation of Indiana No Drawing. Application July 5, 1929 Serial No; 376,290 1 9 Claims.
The present invention relates to improvements in desulphurizing hydrocarbon oils, and more particularly the lower boiling point distillates such as distillates in the gasoline and kerosene boiling point range. It has been found particularly suited for use in connection with cracked distillates from high sulphur oil, such as Lander and Winkler oils which distillates contain sulphur bodies of a highly refractory type and which are diflicult to remove.
In accordance with the present invention, the alkali metals such as sodium and potassium are preferably employed to effect the desulphurizing. The metal used may be employed in lumps (massive) in operating in accordance with the present invention, and metals fusible at the temperature of operation are then preferred.
In carrying out the invention, the active metal is employed in a proportion equal to or substantially exceeding the atomic equivalent of the amount of sulphur present. In general, the atomic proportion of the metal to the sulphur should exceed 1 to 1, and proportions in excess of 3 to 1 are preferred. The distillate and the active metal are heated together to a temperature of at least 400 F. and preferably not exceeding 650 F. In general a temperature of at least 500 F. is preferred. The operation is conducted under pressure, generally in excess of 150 lbs. per sq. in. and preferably from 200 'to 300 lbs. per sq. in. Higher pressures are employed when lower boiling constituents are present. Under these temperature and pressure conditions the distillate is of course substantially in the liquid state and the alkali metal is in the molten condition.
As an example of the operation, a gasoline derived by a vapor phase cracking operation from a high sulphur crude oil was treated with lump sodium, the atomic ratio of sodium to sulphur being 4 to 1 at a temperature of 575 F. and a pressure of 290 lbs. per sq. in. for three hours with vigorous agitation, the percentage of sulphur being reduced from an initial value of 0.182 to 0.087. The same gasoline treated with a higher proportion of sodium, the atomic proportion of sodium to sulphur being 6.3 to l, at 575 F. under 300 lbs. per sq. in. pressure, the sulphur was reduced to 0.016%.
To further illustrate the invention, the 225 to 420 F. cut of another distillate derived by an ordinary cracking process from a sulphur-containing crude was treated in the presence of an inert substantially sulphur-free heavy oil having an initial boiling point above 600 F. with sodium in an atomic ratio to the sulphur of 4.65 to 1 at a temperature of 560 F. and a pressure of 175 lbs., the sulphur content being reduced from 0.473% to about 0.1%. It is thus apparent that the admixture of a heavy oil which, has an initial boiling point substantially above the end point of the distillate oil and is therefore readily separable from the low boiling distillate, improves the effectiveness of the action of the active metal.
Other alkali metals, such as lithium, potassium and the like are similarly efiective.
When sodium or other active alkali metal is employed in lump form, it may be screened or otherwise separated out of the treated oil and reused for the treatment of fresh sulphurcontaining distillate, suflicient additional fresh metal being supplied to bring the atomic ratio of metal to sulphur to the desired figure. However, since more sodium is apparently used up in the reaction than that calculated from the amount of sulphur removed, an excess over such calculated amount should be supplied for replenishment or the amount of sodium present will be insufficient to effect the desired desulphurization. Thus, in an operation conducted with sodium in lump form in an atomic ratio relative to the sulphur of 4 to 1 on a sulphurcontaining pressure distillate out having an approximate boiling range of from 225 to 420 F., at a temperature of 575 F. and a pressure of 235 lbs. per sq. in. for three hours, in the first use of the sodium, the sulphur was reduced from an initial percentage of 0.764 to 0.067. On the second use, it was reduced from 0.764 to 0.092, and on third use from 0.764 to 0.186. Thus the sodium or other active metal may be reused as long as the amount present is sufficient for effective reaction, additional metal being added as required to maintain effectiveness.
The operation may be conducted in an atmosphere of a gas inert to the oil and alkali metal under the conditions of the process, such as hydrogen or nitrogen. This serves to increase the effectiveness of sulphur removal with a given ratio of metal to sulphur.
I claim:
1. In a process of desulphurizing a low boiling hydrocarbon distillate lying substantially within the gasoline-kerosene boiling point range the step which consists in coagitating said distillate, in substantially liquid state, and an alkali metal in molten form at a temperature substantially within the range of 450 F. to 650 F. under a pressure of at least about 150 pounds per square inch.
2. The process as in claim 1 in which the alkali metal is metallic sodium.
3. The process as in claim 1 wherein the distillate prior to treatment with the alkali metal, is admixed with a low sulphur oil, the initial boiling point of which is substantially above the end point of said distillate.
4. The process as in claim 1 wherein the distillate and alkali metal are coagitated in an atmosphere of a gas inert to the oil and alkali metal under the conditions of the process.
5. The process as in claim 1 wherein the excess alkali metal is separated from the treated distillate, and coagitated with a fresh portion of untreated distillate and a fresh portion of alkali metal under said conditions of temperaa ture and pressure. p
6. The process as in claim 1 in which at 7 .inch.
8. The process as in claim '7 in which the alkali metal is metallic sodium.
9. The process as in claim 7 in which at least three atoms of alkali metal are used for every atom of sulphur in the distillate to be desulphurized.
ROBERT F. RUTHRUFF.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US376290A US1938672A (en) | 1929-07-05 | 1929-07-05 | Desulphurizing hydrocarbon oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US376290A US1938672A (en) | 1929-07-05 | 1929-07-05 | Desulphurizing hydrocarbon oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US1938672A true US1938672A (en) | 1933-12-12 |
Family
ID=23484401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US376290A Expired - Lifetime US1938672A (en) | 1929-07-05 | 1929-07-05 | Desulphurizing hydrocarbon oils |
Country Status (1)
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Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2772211A (en) * | 1953-05-28 | 1956-11-27 | Ethyl Corp | Treatment of hydrocarbon stocks with sodium |
US2879241A (en) * | 1955-03-10 | 1959-03-24 | Petrolite Corp | Process of oxidizing mixture of microcrystalline wax, an ester of monocarboxylated polyethylene and polyethylene, and product produced thereby |
US2960546A (en) * | 1957-03-11 | 1960-11-15 | Nat Distillers Chem Corp | Desulfurization of aromatic hydrocarbons |
US3755149A (en) * | 1971-06-09 | 1973-08-28 | Sun Oil Co Pennsylvania | Process for desulfurizing petroleum resids |
US4076613A (en) * | 1975-04-28 | 1978-02-28 | Exxon Research & Engineering Co. | Combined disulfurization and conversion with alkali metals |
US4119528A (en) * | 1977-08-01 | 1978-10-10 | Exxon Research & Engineering Co. | Hydroconversion of residua with potassium sulfide |
DE3114766A1 (en) * | 1980-04-15 | 1982-06-16 | Rollan Dr. 89316 Eureka Nev. Swanson | METHOD FOR CONVERTING COAL OR Peat TO GASEOUS HYDROCARBONS OR VOLATILE DISTILLATES OR MIXTURES THEREOF |
US4366045A (en) * | 1980-01-22 | 1982-12-28 | Rollan Swanson | Process for conversion of coal to gaseous hydrocarbons |
US4468316A (en) * | 1983-03-03 | 1984-08-28 | Chemroll Enterprises, Inc. | Hydrogenation of asphaltenes and the like |
US4545891A (en) * | 1981-03-31 | 1985-10-08 | Trw Inc. | Extraction and upgrading of fossil fuels using fused caustic and acid solutions |
US5059307A (en) * | 1981-03-31 | 1991-10-22 | Trw Inc. | Process for upgrading coal |
US5085764A (en) * | 1981-03-31 | 1992-02-04 | Trw Inc. | Process for upgrading coal |
WO1997046638A1 (en) * | 1996-06-04 | 1997-12-11 | Exxon Research And Engineering Company | Process for desulfurization of petroleum feeds |
US6053963A (en) * | 1998-05-21 | 2000-04-25 | Gnb Technologies, Inc. | Method for treating rotary slag |
US20090134059A1 (en) * | 2005-12-21 | 2009-05-28 | Myers Ronald D | Very Low Sulfur Heavy Crude oil and Porcess for the Production thereof |
US8951491B2 (en) | 2013-01-03 | 2015-02-10 | Council Of Scientific & Industrial Research | Process for the adsorption of toxic sulphur bearing gases |
US9410042B2 (en) | 2012-03-30 | 2016-08-09 | Aditya Birla Science And Technology Company Ltd. | Process for obtaining carbon black powder with reduced sulfur content |
US9873797B2 (en) | 2011-10-24 | 2018-01-23 | Aditya Birla Nuvo Limited | Process for the production of carbon black |
US20180251687A1 (en) * | 2011-03-23 | 2018-09-06 | Ski Carbon Black (India) Private Limited | Process for the desulfurization of petroleum oil |
-
1929
- 1929-07-05 US US376290A patent/US1938672A/en not_active Expired - Lifetime
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2772211A (en) * | 1953-05-28 | 1956-11-27 | Ethyl Corp | Treatment of hydrocarbon stocks with sodium |
US2879241A (en) * | 1955-03-10 | 1959-03-24 | Petrolite Corp | Process of oxidizing mixture of microcrystalline wax, an ester of monocarboxylated polyethylene and polyethylene, and product produced thereby |
US2960546A (en) * | 1957-03-11 | 1960-11-15 | Nat Distillers Chem Corp | Desulfurization of aromatic hydrocarbons |
US3755149A (en) * | 1971-06-09 | 1973-08-28 | Sun Oil Co Pennsylvania | Process for desulfurizing petroleum resids |
US4076613A (en) * | 1975-04-28 | 1978-02-28 | Exxon Research & Engineering Co. | Combined disulfurization and conversion with alkali metals |
US4119528A (en) * | 1977-08-01 | 1978-10-10 | Exxon Research & Engineering Co. | Hydroconversion of residua with potassium sulfide |
US4366045A (en) * | 1980-01-22 | 1982-12-28 | Rollan Swanson | Process for conversion of coal to gaseous hydrocarbons |
DE3114766A1 (en) * | 1980-04-15 | 1982-06-16 | Rollan Dr. 89316 Eureka Nev. Swanson | METHOD FOR CONVERTING COAL OR Peat TO GASEOUS HYDROCARBONS OR VOLATILE DISTILLATES OR MIXTURES THEREOF |
US5059307A (en) * | 1981-03-31 | 1991-10-22 | Trw Inc. | Process for upgrading coal |
US4545891A (en) * | 1981-03-31 | 1985-10-08 | Trw Inc. | Extraction and upgrading of fossil fuels using fused caustic and acid solutions |
US5085764A (en) * | 1981-03-31 | 1992-02-04 | Trw Inc. | Process for upgrading coal |
US4468316A (en) * | 1983-03-03 | 1984-08-28 | Chemroll Enterprises, Inc. | Hydrogenation of asphaltenes and the like |
WO1997046638A1 (en) * | 1996-06-04 | 1997-12-11 | Exxon Research And Engineering Company | Process for desulfurization of petroleum feeds |
US6210564B1 (en) * | 1996-06-04 | 2001-04-03 | Exxon Research And Engineering Company | Process for desulfurization of petroleum feeds utilizing sodium metal |
US6053963A (en) * | 1998-05-21 | 2000-04-25 | Gnb Technologies, Inc. | Method for treating rotary slag |
US20090134059A1 (en) * | 2005-12-21 | 2009-05-28 | Myers Ronald D | Very Low Sulfur Heavy Crude oil and Porcess for the Production thereof |
US20180251687A1 (en) * | 2011-03-23 | 2018-09-06 | Ski Carbon Black (India) Private Limited | Process for the desulfurization of petroleum oil |
US9873797B2 (en) | 2011-10-24 | 2018-01-23 | Aditya Birla Nuvo Limited | Process for the production of carbon black |
US9410042B2 (en) | 2012-03-30 | 2016-08-09 | Aditya Birla Science And Technology Company Ltd. | Process for obtaining carbon black powder with reduced sulfur content |
US8951491B2 (en) | 2013-01-03 | 2015-02-10 | Council Of Scientific & Industrial Research | Process for the adsorption of toxic sulphur bearing gases |
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