US2030033A - Treatment of cracked petroleum distillates - Google Patents
Treatment of cracked petroleum distillates Download PDFInfo
- Publication number
- US2030033A US2030033A US675297A US67529733A US2030033A US 2030033 A US2030033 A US 2030033A US 675297 A US675297 A US 675297A US 67529733 A US67529733 A US 67529733A US 2030033 A US2030033 A US 2030033A
- Authority
- US
- United States
- Prior art keywords
- cracked petroleum
- hydroxy
- hydroxyquinoline
- treatment
- petroleum distillates
- 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
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S292/00—Closure fasteners
- Y10S292/25—Remote control
Definitions
- This invention relates to petroleum products manufacture, and more particularly motor fuels; and it is among the objects of the invention to provide a treatment inhibitive of gum-formation which is not diificult or critical to apply, and which is desirably dependable in the conditions .encounterable generally.
- the invention comprises the 10 features hereinafter fully described, and particularly pointed out in the claims, .the following description setting forth in detail certain em-' bodiments of the invention, these being indicative however, of but a few of the various ways 'in which the principle of the invention may be employed.
- the cracked petroleum distillate is subjected to the action of a hydroxyquinoline.
- a hydroxyquinoline Representative of such com- 20 pounds for example, are 8-hydroxyquinollne, 2- hydroxyquinoline, G-hydroxyquinoline, 7-hydroxyquinoline; also tetrahydro-derivatives, such as 2 hydroxytetrahydroquinoline, 6 hydroxytetrahydroquinoline, 7 hydroxytetrahydroquinoline, 25 8-hydroxytetrahydroquinline, etc.
- the amount of the treating agent is small, less than 1 percent and in general 0.004 to 0.5 per cent.
- the treating agent may be dissolved directly in the distillate to he treated, or where preferred may be dissolved in an organic solvent such as alcohol, benzol or the like, and such. solution may thenbe incorporated with the distillate.
- 250 gr. of 8-hydroxyquinoline is incorporated in each 1000 gal- 35 ions of cracked gasoline, and is thoroughly disseminated.
- a process of inhibiting gum-formation in cracked petroleum distillates which comprises subjecting such distillate to the action of a small amount of an agent selected from the group consisting of 8-hydroxy quinoline, Z-hydroxy quinoline, fi-hydroxy quinoline, 'I-hydroxy quinoline, 2-hydroxy tetrahydroquinoline, G-hydroxy tetrahydroquinoline, 7-hydroxy tetrahydroquinoline, 8-hydroxy tetrahydroquinoline.
- a process of inhibiting gum-formation in cracked petroleum distillates which comprises subjecting such distillate to the action of a small amount of 8-hydroxyquinoline.
- a process of inhibiting gum-formation in cracked petroleum distillates which comprises subjecting such distillate to the action of a small amount of 2-hydroxyquinoline.
- a processof inhibiting gum-formation in cracked petroleum distillates which comprises subjecting such distillate to the action of a small amount of fi-hydroxyquinoline.
- a cracked petroleum motor fuel treated with a small amount ofan agent selected from the group consisting of B-hydroxy quinoline, Z-hydroxy quinoline, 6-hydroxy quinoline, 7-hydroxy quinoline, 2-hydroxy tetrahydroquinoline, 6-hy- 'droxy. tetrahydroquinoline, '7-hydroxy tetrahydroquinoline, 8'-hydroxy tetrahydroquinoline.
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)
- Other In-Based Heterocyclic Compounds (AREA)
Description
Patented Feb. 4, i936 STAS UNHTE NT QFECE TREATMENT or CRACKED ra'rnoLn DISTILLATES 1 No Drawing. Application June 10, 1933, Serial No. 675,297
8 Claims.
This invention relates to petroleum products manufacture, and more particularly motor fuels; and it is among the objects of the invention to provide a treatment inhibitive of gum-formation which is not diificult or critical to apply, and which is desirably dependable in the conditions .encounterable generally.
. To the accomplishment of the foregoing and related ends, the invention, then, comprises the 10 features hereinafter fully described, and particularly pointed out in the claims, .the following description setting forth in detail certain em-' bodiments of the invention, these being indicative however, of but a few of the various ways 'in which the principle of the invention may be employed.
In accordance with my invention, the cracked petroleum distillate is subjected to the action of a hydroxyquinoline. Representative of such com- 20 pounds for example, are 8-hydroxyquinollne, 2- hydroxyquinoline, G-hydroxyquinoline, 7-hydroxyquinoline; also tetrahydro-derivatives, such as 2 hydroxytetrahydroquinoline, 6 hydroxytetrahydroquinoline, 7 hydroxytetrahydroquinoline, 25 8-hydroxytetrahydroquinline, etc. The amount of the treating agent is small, less than 1 percent and in general 0.004 to 0.5 per cent. The treating agent may be dissolved directly in the distillate to he treated, or where preferred may be dissolved in an organic solvent such as alcohol, benzol or the like, and such. solution may thenbe incorporated with the distillate.
As an illustrative example: 250 gr. of 8-hydroxyquinoline is incorporated in each 1000 gal- 35 ions of cracked gasoline, and is thoroughly disseminated.
As another example: 250 gr. of 2*hydr0xyquinoline is dissolved in a solvent, as alcohol, to make up substantially one gallon volume, and
this is mixed into each 1000 gallons of cracked gasoline to be treated.
Other modes of applying the principle of the invention may be employed, change being made as regards the details described, provided the features stated in any of the following claims, or the equivalent of such,-be employed.
I therefore particularly-point out and distinctly claim as my invention:-
.1. A process of inhibiting gum-formation in cracked petroleum distillates, which comprises subjecting such distillate to the action of a small amount of an agent selected from the group consisting of 8-hydroxy quinoline, Z-hydroxy quinoline, fi-hydroxy quinoline, 'I-hydroxy quinoline, 2-hydroxy tetrahydroquinoline, G-hydroxy tetrahydroquinoline, 7-hydroxy tetrahydroquinoline, 8-hydroxy tetrahydroquinoline.
2. A process of inhibiting gum-formation in cracked petroleum distillates, which comprises subjecting such distillate to the action of a small amount of 8-hydroxyquinoline.
3. A process of inhibiting gum-formation in cracked petroleum distillates, which comprises subjecting such distillate to the action of a small amount of 2-hydroxyquinoline.
4. A processof inhibiting gum-formation in cracked petroleum distillates, which comprises subjecting such distillate to the action of a small amount of fi-hydroxyquinoline. c
5. A cracked petroleum motor fuel treated with a small amount ofan agent selected from the group consisting of B-hydroxy quinoline, Z-hydroxy quinoline, 6-hydroxy quinoline, 7-hydroxy quinoline, 2-hydroxy tetrahydroquinoline, 6-hy- 'droxy. tetrahydroquinoline, '7-hydroxy tetrahydroquinoline, 8'-hydroxy tetrahydroquinoline.
6. A cracked petroleum motor fuel treated with a small amount of B-hydroxyquinoline.
' 7. A cracked petroleum motor fuel treated with a small amount of 2-hydroxyquinoline.
8; A cracked petroleum motor fuel treated with a small amount of G-hydroxyquinoline.
ELLIOTT B,v McCONNEIL.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US675297A US2030033A (en) | 1933-06-10 | 1933-06-10 | Treatment of cracked petroleum distillates |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US675297A US2030033A (en) | 1933-06-10 | 1933-06-10 | Treatment of cracked petroleum distillates |
Publications (1)
Publication Number | Publication Date |
---|---|
US2030033A true US2030033A (en) | 1936-02-04 |
Family
ID=24709860
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US675297A Expired - Lifetime US2030033A (en) | 1933-06-10 | 1933-06-10 | Treatment of cracked petroleum distillates |
Country Status (1)
Country | Link |
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US (1) | US2030033A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2562970A (en) * | 1950-04-14 | 1951-08-07 | Thompson Chester Ray | Preservation of forage crops |
US2573779A (en) * | 1944-04-10 | 1951-11-06 | Shell Dev | Color stabilizers |
US2637636A (en) * | 1944-04-10 | 1953-05-05 | Shell Dev | Color stabilizers |
US2647824A (en) * | 1949-01-26 | 1953-08-04 | Standard Oil Dev Co | Stabilized compositions containing hydrogenated quinolines with oxidation inhibitors |
US2881061A (en) * | 1956-03-12 | 1959-04-07 | Socony Mobil Oil Co Inc | Anti-knock gasoline containing hydrogenated quinolines and indoles |
US2892166A (en) * | 1955-01-20 | 1959-06-23 | Westinghouse Electric Corp | Additive for dielectric fluid of transformer assembly |
US2930680A (en) * | 1957-11-08 | 1960-03-29 | Exxon Research Engineering Co | Fuels containing wear-reducing and rust preventing additives |
US2933379A (en) * | 1958-01-16 | 1960-04-19 | Standard Oil Co | Stabilized motor fuel |
US3307970A (en) * | 1961-11-30 | 1967-03-07 | Merck & Co Inc | Preparations for the production of metal 8-hydroxy quinolinates and process for utilizing same |
WO1989011518A2 (en) | 1988-05-18 | 1989-11-30 | National Research Development Corporation | Method of and compositions for reducing wear on surfaces subjected to frictional forces |
US4941968A (en) * | 1989-07-28 | 1990-07-17 | Betz Laboratories, Inc. | Method for inhibiting gum formation in liquid hydrocarbon mediums |
-
1933
- 1933-06-10 US US675297A patent/US2030033A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2573779A (en) * | 1944-04-10 | 1951-11-06 | Shell Dev | Color stabilizers |
US2637636A (en) * | 1944-04-10 | 1953-05-05 | Shell Dev | Color stabilizers |
US2647824A (en) * | 1949-01-26 | 1953-08-04 | Standard Oil Dev Co | Stabilized compositions containing hydrogenated quinolines with oxidation inhibitors |
US2562970A (en) * | 1950-04-14 | 1951-08-07 | Thompson Chester Ray | Preservation of forage crops |
US2892166A (en) * | 1955-01-20 | 1959-06-23 | Westinghouse Electric Corp | Additive for dielectric fluid of transformer assembly |
US2881061A (en) * | 1956-03-12 | 1959-04-07 | Socony Mobil Oil Co Inc | Anti-knock gasoline containing hydrogenated quinolines and indoles |
US2930680A (en) * | 1957-11-08 | 1960-03-29 | Exxon Research Engineering Co | Fuels containing wear-reducing and rust preventing additives |
US2933379A (en) * | 1958-01-16 | 1960-04-19 | Standard Oil Co | Stabilized motor fuel |
US3307970A (en) * | 1961-11-30 | 1967-03-07 | Merck & Co Inc | Preparations for the production of metal 8-hydroxy quinolinates and process for utilizing same |
WO1989011518A2 (en) | 1988-05-18 | 1989-11-30 | National Research Development Corporation | Method of and compositions for reducing wear on surfaces subjected to frictional forces |
WO1989011518A3 (en) * | 1988-05-18 | 1990-02-08 | Nat Res Dev | Method of and compositions for reducing wear on surfaces subjected to frictional forces |
AU622912B2 (en) * | 1988-05-18 | 1992-04-30 | British Technology Group Limited | Method of and compositions for reducing wear on surfaces subjected to frictional forces |
US4941968A (en) * | 1989-07-28 | 1990-07-17 | Betz Laboratories, Inc. | Method for inhibiting gum formation in liquid hydrocarbon mediums |
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