US1938671A - Desulphurizing hydrocarbon oils - Google Patents
Desulphurizing hydrocarbon oils Download PDFInfo
- 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
Links
- 239000003921 oil Substances 0.000 title description 10
- 239000004215 Carbon black (E152) Substances 0.000 title description 2
- 229930195733 hydrocarbon Natural products 0.000 title description 2
- 150000002430 hydrocarbons Chemical class 0.000 title description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 29
- 239000005864 Sulphur Substances 0.000 description 29
- 238000009835 boiling Methods 0.000 description 13
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 238000005336 cracking Methods 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241000276489 Merlangius merlangus Species 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000012808 vapor phase Substances 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
- 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
- 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 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.
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)
| 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 |
-
1929
- 1929-07-05 US US376277A patent/US1938671A/en not_active Expired - Lifetime
Cited By (3)
| 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 |
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