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US1938670A - Desulphurizing hydrocarbon oils - Google Patents

Desulphurizing hydrocarbon oils Download PDF

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Publication number
US1938670A
US1938670A US326407A US32640728A US1938670A US 1938670 A US1938670 A US 1938670A US 326407 A US326407 A US 326407A US 32640728 A US32640728 A US 32640728A US 1938670 A US1938670 A US 1938670A
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US
United States
Prior art keywords
sodium
distillate
oil
sulphur
alkali 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
Application number
US326407A
Inventor
Jr Frederick W Sullivan
Arthur B Brown
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Co
Original Assignee
Standard Oil Co
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Filing date
Publication date
Application filed by Standard Oil Co filed Critical Standard Oil Co
Priority to US326407A priority Critical patent/US1938670A/en
Application granted granted Critical
Publication of US1938670A publication Critical patent/US1938670A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G29/00Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
    • C10G29/02Non-metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G19/00Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G29/00Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
    • C10G29/04Metals, or metals deposited on a carrier

Definitions

  • Another factor which has considerable influcompleteness of the sulphur removal is the amount of metal which isemployed. It is found that a substantial excess of the metal gives much more complete removal of sulphur than does a smaller amount of metal under the same conditions. We prefer to employ the metal to the extent of between one and two equivalents of the sulphur content and to control the temperature to give the desired amount of desulphurization.
  • the heat treatment should be effected under pressure in order to insure effective treatment.
  • Example I Winkler gas oil of a boiling range between 500 and 675 F. and containing 1.18% of sulphur is passed through a colloid mill of which the plates 55 are set at .002 inches clearance, together with ence upon the rapidity of the reaction and the molten sodium in the requisite quantity. In this way, the sodium is brought into a highly dispersed state of very permanent character.
  • This oil is heated in a batch still for three hours and thereafter the sodium sulphide is permitted to settle 6i) and the distillate drawn ofi. As indicated above, pressure is maintained, where necessary, to prevent the liquid boiling off.
  • the following table gives the sulphur content at various temperatures and with various amounts of sodium.

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  • 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 PATIENT OFFICE UNITED STATES DESULPH'URIZING HYDROCARBON OILS Frederick W. Sullivan, Jr., Whiting, and Arthur B.- Brown, Hammond; Ind., assignors to Standard Oil Company, Whiting, Ind., a corporation of Indiana No Drawing. Application December 15, 1928 \Serial No. 326,407
Claims. (Cl. 19626) purpose are the alkali metals and particularly sodium and potassiuma In actual practice,we prefer to employ sodium on account of its cheapness and effectiveness.
In practice, we prefer to subje ct the oil containing the highly dispersed metal to heating for a substantial time, for example, two to four hours, more or less, at temperatures between 350 to 650 F. It must be understood that the invention is not intended to be limited to the periods or temperatures set forth, since the reaction will take place at higher and lower temperatures and the time may be varied in accordance with the temperature employed and, also, the extent of desulphurizing which it is desired to obtain.
Another factor which has considerable influcompleteness of the sulphur removal is the amount of metal which isemployed. It is found that a substantial excess of the metal gives much more complete removal of sulphur than does a smaller amount of metal under the same conditions. We prefer to employ the metal to the extent of between one and two equivalents of the sulphur content and to control the temperature to give the desired amount of desulphurization.
It will be understood that smaller amounts of metal may be employed where a lesser degree of sulphur removal is desired.
In the case of low boiling distillates which are to be heated above the temperature at which at least a part of the oil vaporizes, the heat treatment should be effected under pressure in order to insure effective treatment.
The invention will be readily understood from the following specific examples.
Example I Winkler gas oil of a boiling range between 500 and 675 F. and containing 1.18% of sulphur is passed through a colloid mill of which the plates 55 are set at .002 inches clearance, together with ence upon the rapidity of the reaction and the molten sodium in the requisite quantity. In this way, the sodium is brought into a highly dispersed state of very permanent character. This oil is heated in a batch still for three hours and thereafter the sodium sulphide is permitted to settle 6i) and the distillate drawn ofi. As indicated above, pressure is maintained, where necessary, to prevent the liquid boiling off. The following table gives the sulphur content at various temperatures and with various amounts of sodium.
1.5 equiv- 2equiva- 2% equiv- 3equiva- Temp. F. alents o1 lents of alents of lents oi sodium sodium sodium sodium Example If Lander gas oil containing 1.804% of sulphur 1 equivalent of sodium 1.5 equiv- 2 equivaalents of lents of sodium Temperature sodium Although the present invention has been described in connection with the details of specific examples thereof, it is not intended that such details shall be regarded as limitations upon the scope of the invention, except in so far as included in the accompanying claims.
We claim:
1. The method of desulphurizing petroleum distillates while in a liquid state which consists in passing the distillate and molten alkali metal through a colloid mill to disperse the alkali metal therethrough in the form of a colloidal suspension, heating the distillate to cause the alkali metal to react with the sulphur contained in said distillate, and separating the alkali metal sulphide from the treated oil.
2. The method of substantially desulphurizing petroleum-oil distillates while in a liquid state which consists in passing the distillate through a colloid mill, together with molten sodium, thereby dispersing the sodium in the oil in a finely divided colloidal condition, heating the distillate while in the liquid state to cause the colloidal-sodium to react with the sulphur contained a. The method of desulphuri'zing petroleum dis-- tillates while in a liquid state which consists in passing the liquid distillate together with molten alkali metal through a colloid mill to disperse the alkali metal therethrough in a highly dispersed state, heating the distillate to between 350 and 650 F. for suflicient time to cause a substantial part of the sulphur contained in the distillate to combine with the dispersed alkali metal, and separating the alkali metal sulphide from the treated oil.
4. The method of desulphurizing petroleum distillates while in a liquid state, which consists in passing the distillate together with molten sodium through a colloid mill to disperse the sodium therethrough in a highly dispersed state, the amount of sodium being from 1% to 3 times the equivalent of the sulphur-in the distillate, heating the distillate to between 350 and 650 F. for suflicient time to cause a substantial part'ot the sulphur contained in the distillate to combine with the sodium, maintaining sumcient pressure upon the distillate during the heating thereof to maintain said distillatein a liquid state, and then separating the sodium sulphide from the treated distillate.
' 5. The method of desulphurizing gas oil while in the liquid phase, which consists in passing said oil through a colloid mill together with a molten alkali metal, thereby dispersing the alkali metal therethrough in a highly dispersed state, heating the oil to cause the alkali metal to react with the sulphur in said oil, and separating the solid reaction products and residue from the treated oil.
FREDERICK W. SULLIVAN. JR. ARTHUR B. BROWN.
US326407A 1928-12-15 1928-12-15 Desulphurizing hydrocarbon oils Expired - Lifetime US1938670A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US326407A US1938670A (en) 1928-12-15 1928-12-15 Desulphurizing hydrocarbon oils

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2614967A (en) * 1949-07-28 1952-10-21 Standard Oil Dev Co Petroleum oil refining process
US2614966A (en) * 1950-05-01 1952-10-21 Standard Oil Dev Co Sodium refining of petroleum oils
US2748058A (en) * 1953-07-29 1956-05-29 Du Pont Desulfurization of petroleum products with alkali metal followed by aqueous formaldehyde
US2759896A (en) * 1951-09-28 1956-08-21 Ethyl Corp Process of treating metal mixtures
US2772211A (en) * 1953-05-28 1956-11-27 Ethyl Corp Treatment of hydrocarbon stocks with sodium
DE1105543B (en) * 1959-11-14 1961-04-27 Degussa Process for the regeneration of waste oils

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2614967A (en) * 1949-07-28 1952-10-21 Standard Oil Dev Co Petroleum oil refining process
US2614966A (en) * 1950-05-01 1952-10-21 Standard Oil Dev Co Sodium refining of petroleum oils
US2759896A (en) * 1951-09-28 1956-08-21 Ethyl Corp Process of treating metal mixtures
US2772211A (en) * 1953-05-28 1956-11-27 Ethyl Corp Treatment of hydrocarbon stocks with sodium
US2748058A (en) * 1953-07-29 1956-05-29 Du Pont Desulfurization of petroleum products with alkali metal followed by aqueous formaldehyde
DE1105543B (en) * 1959-11-14 1961-04-27 Degussa Process for the regeneration of waste oils

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