[go: up one dir, main page]

US1938671A - Desulphurizing hydrocarbon oils - Google Patents

Desulphurizing hydrocarbon oils Download PDF

Info

Publication number
US1938671A
US1938671A US376277A US37627729A US1938671A US 1938671 A US1938671 A US 1938671A US 376277 A US376277 A US 376277A US 37627729 A US37627729 A US 37627729A US 1938671 A US1938671 A US 1938671A
Authority
US
United States
Prior art keywords
sulphur
pressure
lbs
per
distillate
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
US376277A
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
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Standard Oil Co filed Critical Standard Oil Co
Priority to US376277A priority Critical patent/US1938671A/en
Application granted granted Critical
Publication of US1938671A publication Critical patent/US1938671A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C10G29/00Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
    • C10G29/04Metals, 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 may be employed preferably in dispersed form; for example, in such a high degree of dispersion as is secured by the use of the colloid mill.
  • the active metal is employed in a proportion equal to or substantially exceeding the atomic equivalent of the amount of sulphur present.
  • the atomic ratio 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 350 F., and preferably not exceeding 650 F.
  • the operation is conducted under pressure, with low boiling distillates 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.
  • a gasoline derived by a vapor phase cracking operation from a high sulphur crude oil was treated with 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, the percentage of sulphur being reduced from an initial value of 0.182 to 0.087.
  • the 225 F. to 420 F. cut of another distillate derived by an ordinary cracking process from a sulphurcontaining crude was treated with sodium in an atomic ratio relative to the sulphur of 4 to 1 at a temperature of 550 F. and a pressure of 240 lbs. per sq. in, the sulphur content being reduced from 0.339% to 0.207%.
  • the same cut treated with sodium in the atomic ratio of 6'to 1 at a temperature of 575 .F. and a pressure of 280 lbs. per sq. in. had its sulphur content reduced to 0.039%.
  • alkali metals such as lithium, potassium and the like are similarly efiective.

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 UNITED STATES 1,938,671 DESULPI'IURIZHING HYDROOARBON OILS Frederick W. Sullivan, .Jr., and Arthur,B.-Brown, Hammond, Ind., assignors to Standard Oil Company, Whiting, Ind, a corporation of Indiana No Drawing. Application July 5, 1929 Serial No. 376,277
4 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 may be employed preferably in dispersed form; for example, in such a high degree of dispersion as is secured by the use of the colloid mill.
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 ratio 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 350 F., and preferably not exceeding 650 F. The operation is conducted under pressure, with low boiling distillates 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.
As an example of the operation, a gasoline derived by a vapor phase cracking operation from a high sulphur crude oil was treated with 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, 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 ratio of sodium to sulphur being 6.3, at 575 F. under 300 lbs. per sq. in. pressure, the sulphur was reduced to 0.016%.
In carrying out the operation to desulphurize oils in the gasoline boiling point range, it has been found desirable to separate the lower boiling portions of the distillate; that is, the portions coming over below 200 F. to 325 F. and which is ordinarily satisfactorily low in sulphur content, and to treat only the cut remaining. In treating the heavier cut produced in this Way, it has been found that a lower proportion of the active metal is required and lower pressures may be employed than when the entire gasoline is treated. Thus, with the same gasoline as that employed in the illustrative example above, the gasoline was cut by distillation into two fractions at 225 F. The lower boiling fraction, from the initial boiling point to 225 F, had a sulphur content without treatment of 0.058%. The higher boiling cut from 225 F. to 420 F. was adequately desulphurized with sodium in an atomic ratio relative to the sulphur of 3.25 at a temperature of 550 F. and a pressure of about 250 lbs. per sq. in. The point at which the cut is made between the lighter and heavier fractions obviously varies with different oils in accordance with the distribution of the sulphur; thus, with some oils it has been found satisfactory to make the out at 325 F. The proper point may be readily determined by determining the sulphur distribution in the different cuts of the oil experimentally, and thus determining the proper temperature at which a maximum lower boiling fraction has a satisfactorily low sulphur content.
To further illustr'ate the invention, the 225 F. to 420 F. cut of another distillate derived by an ordinary cracking process from a sulphurcontaining crude was treated with sodium in an atomic ratio relative to the sulphur of 4 to 1 at a temperature of 550 F. and a pressure of 240 lbs. per sq. in, the sulphur content being reduced from 0.339% to 0.207%. The same cut treated with sodium in the atomic ratio of 6'to 1 at a temperature of 575 .F. and a pressure of 280 lbs. per sq. in. had its sulphur content reduced to 0.039%.
Other alkali metals, such as lithium, potassium and the like are similarly efiective. Thus a 225 F. to 420 F. cut of a sulphur-containing pressure distillate, on treatment with potassium in the atomic ratio of 4.2 to 1 at 575 F. and 250 lbs. per sq. in. pressure for three hours had its sulphur content reduced from 0.781% to 0.014%. A 325 F. to 420 F. cut, of another distillate, treated with potassium in the atomic ratio of 5.5 to 1 at a temperature of about 630 F. and a pressure of about 250 lbs. per sq. in. for three hours had its sulphur content reduced from 1.105% to 0.021%.
We claim:
1. In a process of desulphurizing a pressure 105 distillate having an objectionably high sulphur content, the sulphur content of successively higher boilingfractions of said distillate increasing in general with the boiling point, the steps which consist in :Eractionally redistilling said dis- 110 tillate, discontinuing theredistillation when the temperature has risen to a point approximately within the range 200 F. to 325 F., coagitating the bottoms from said redistillation with an alkali metal at a temperature of from 350 F. to 650 F. under a pressure in excess of 150 lbs. per sq. in. to reduce its sulphur content to an unobjectionable point and reblending the treated bottoms with the overhead from said redistillation.
2. In a process of desulphurizing a pressure distillate having an objectionably high sulphur content, the sulphur content of successively higher boiling fractions of said distillate increasing in general with the boiling point, the steps which consist in fractionally redistilling said distillate, discontinuing the redistillation when the the temperature has risen to a point approximately within the range 200 F. to 325 F., coagitating the bottoms from said redistillation with metallic sodium at a temperature of from about 350 F. to about 650 F. under a pressure in excess of about 150 lbs. per sq. in. to reduce its sulphur content to an unobjectionable point and reblending the treated bottoms with the overhead from said redistillation.
3. Process steps according to claim 1 in which said alkali metal is used in a quantity of at least three atoms for every atom of sulphur in said bottoms.
4. Process steps according to claim 2 in which said alkali metal is used in a quantity of at least three atoms for every atom of sulphur in said bottoms.
FREDERICK W. SULLIVAN, JR. ARTHUR B. BROWN.
US376277A 1929-07-05 1929-07-05 Desulphurizing hydrocarbon oils Expired - Lifetime US1938671A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US376277A US1938671A (en) 1929-07-05 1929-07-05 Desulphurizing hydrocarbon oils

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US376277A US1938671A (en) 1929-07-05 1929-07-05 Desulphurizing hydrocarbon oils

Publications (1)

Publication Number Publication Date
US1938671A true US1938671A (en) 1933-12-12

Family

ID=23484351

Family Applications (1)

Application Number Title Priority Date Filing Date
US376277A Expired - Lifetime US1938671A (en) 1929-07-05 1929-07-05 Desulphurizing hydrocarbon oils

Country Status (1)

Country Link
US (1) US1938671A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US6210564B1 (en) * 1996-06-04 2001-04-03 Exxon Research And Engineering Company Process for desulfurization of petroleum feeds utilizing sodium metal

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US6210564B1 (en) * 1996-06-04 2001-04-03 Exxon Research And Engineering Company Process for desulfurization of petroleum feeds utilizing sodium metal

Similar Documents

Publication Publication Date Title
US1938672A (en) Desulphurizing hydrocarbon oils
US3523071A (en) Process for reducing the pour point of shale oil
US1938671A (en) Desulphurizing hydrocarbon oils
US2070295A (en) Treatment of hydrocarbon oils
US1938670A (en) Desulphurizing hydrocarbon oils
US2370533A (en) Cracking and reforming of hydrocarbons
US1954478A (en) Treatment of hydrocarbon oils
US2325115A (en) Desulphurizing hydrocarbon distillate
US2037781A (en) Treatment of hydrocarbon oils
US2270058A (en) Refining of mineral oils
US2280227A (en) Refining of petroleum distillates
US1973499A (en) Treatment of hydrocarbon oils
US1953039A (en) Lubricating oil and process for preparing same
US2257079A (en) Motor fuel
US1920270A (en) Refining and purification of hydrocarbon oils
US1594083A (en) Removal of sulphur and sulphur compounds from hydrocarbon-oil distillates
US2458980A (en) Production of gasoline
US2246760A (en) Stable fuel oil
US2293205A (en) Process for the production of motor fuel
US2094554A (en) Manufacture of motor fuels
US2045262A (en) Refining of hydrocarbon oil
US1974311A (en) Treatment of hydrocarbon oils
US1661566A (en) Motor fuel and process of refining oils
US1963498A (en) Dewaxing hydrocarbon oils
US1970281A (en) Treatment of hydrocarbon oils