GB789857A - Improved petroleum distillate fuels - Google Patents
Improved petroleum distillate fuelsInfo
- Publication number
- GB789857A GB789857A GB10289/56A GB1028956A GB789857A GB 789857 A GB789857 A GB 789857A GB 10289/56 A GB10289/56 A GB 10289/56A GB 1028956 A GB1028956 A GB 1028956A GB 789857 A GB789857 A GB 789857A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzene
- sulphonate
- nitrite
- ammonium
- complex
- 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
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
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2431—Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
- C10L1/2437—Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
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)
- Liquid Carbonaceous Fuels (AREA)
- Lubricants (AREA)
Abstract
A complex is formed by heating an aqueous solution of an ammonium or alkali metal nitrite with a mineral oil solution of a sulphonate at a temperature between 230 DEG and 300 DEG F. until all the water is vaporized. The nitrite may be ammonium, sodium, potassium or lithium nitrite, and the sulphonate may be an ammonium, sodium, potassium, lithium, calcium or barium salt of an alkyl monocyclic or bicyclic aryl sulphonic acid having a molecular weight between 300 and 650 and wherein the alkyl group or groups contain a total number of carbon atoms up to 40. The sulphonate may be a salt of didodecyl benzene, tridodecyl benzene, octadecyl benzene, tetracosyl benzene, hexyl dodecyl benzene or hexyl octadecyl benzene sulphonic acids. 0.1 to 4.0 mols. of the nitrite may be reacted with one mol. of the sulphonate. In an example an aqueous solution of sodium nitrite is reacted with a kerosene solution of ammonium didodecyl benzene sulphonate.ALSO:A fuel composition comprises a major proportion of distillate petroleum hydrocarbons and a minor proportion of a complex formed by reacting a water-soluble ammonium or alkali metal nitrite with an oil-soluble sulphonate. The fuel may be a kerosene, diesel fuel, heating oil or industrial fuel oil, and may contain over 10 per cent by volume of cracked constituents. The nitrite may be ammonium, sodium, potassium or lithium nitrite, and the sulphonate may be an ammonium, sodium, potassium, lithium, calcium or barium salt of an alkyl monocyclic or bicyclic aryl sulphonic acid having a molecular weight between 300 and 650 and wherein the alkyl group or groups contain a total number of carbon atoms up to 40. The sulphonate may be a salt of didodecyl benzene, tridodecyl benzene, octadecyl benzene, tetracosyl benzene, hexyl dodedecyl benzene or hexyl octadecyl benzene sulphonic acids. The complex is prepared by heating 0.1 to 4.0 mols. of the nitrite in aqueous solution per mol. of the sulphonate in an oil solution at a temperature between 230 DEG and 300 DEG F. until all the water is vaporized. The oil solution of the complex is added to the fuel to provide a concentration between 0.002 and 0.3 per cent by weight of the complex in the fuel. An example using a complex of sodium nitrite and ammonium didodecyl benzene sulphonate is given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US511102A US2860040A (en) | 1955-05-25 | 1955-05-25 | Petroleum distillate fuels |
Publications (1)
Publication Number | Publication Date |
---|---|
GB789857A true GB789857A (en) | 1958-01-29 |
Family
ID=24033462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10289/56A Expired GB789857A (en) | 1955-05-25 | 1956-04-04 | Improved petroleum distillate fuels |
Country Status (2)
Country | Link |
---|---|
US (1) | US2860040A (en) |
GB (1) | GB789857A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3505367A (en) * | 1961-02-14 | 1970-04-07 | Henri Brunel | Process for purifying raw sulfonates |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0261958A3 (en) * | 1986-09-24 | 1988-06-15 | Exxon Chemical Patents Inc. | Middle distillate compositions with reduced wax crystal size |
EP0261959B1 (en) * | 1986-09-24 | 1995-07-12 | Exxon Chemical Patents Inc. | Improved fuel additives |
GB2208517B (en) * | 1986-09-24 | 1990-10-03 | Exxon Chemical Patents Inc | Middle distillate compositions with reduced wax crystal size |
US5814110A (en) * | 1986-09-24 | 1998-09-29 | Exxon Chemical Patents Inc. | Chemical compositions and use as fuel additives |
IN184481B (en) * | 1986-09-24 | 2000-08-26 | Exxon Chemical Patents Inc | |
GB2197862B (en) * | 1986-09-24 | 1990-12-05 | Exxon Chemical Patents Inc | Sulphonate derivatives and their use as fuel additives |
IN173485B (en) * | 1986-09-24 | 1994-05-21 | Exxon Chemical Patents Inc | |
WO1988002393A2 (en) * | 1986-09-24 | 1988-04-07 | Exxon Chemical Patents, Inc. | Improved fuel additives |
IN172275B (en) * | 1986-09-24 | 1993-05-29 | Exxon Chemical Patents Inc | |
GB9008811D0 (en) * | 1990-04-19 | 1990-06-13 | Exxon Chemical Patents Inc | Chemical compositions and their use as fuel additives |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2297666A (en) * | 1940-03-09 | 1942-09-29 | Shell Dev | Internal corrosion prevention in conduits |
US2296069A (en) * | 1940-03-21 | 1942-09-15 | Allied Chem & Dye Corp | Fuel for internal combustion engines |
US2527987A (en) * | 1948-03-29 | 1950-10-31 | Shell Dev | Fuel oil composition |
US2623016A (en) * | 1949-01-17 | 1952-12-23 | Union Oil Co | Lubricating oil composition |
US2650198A (en) * | 1950-03-16 | 1953-08-25 | Shell Dev | Oil-soluble petroleum sulfonates |
US2616924A (en) * | 1951-03-16 | 1952-11-04 | Lubrizol Corp | Organic alkaline earth metal complexes and method of making same |
US2695910A (en) * | 1951-05-03 | 1954-11-30 | Lubrizol Corp | Methods of preparation of superbased salts |
BE511937A (en) * | 1951-06-07 |
-
1955
- 1955-05-25 US US511102A patent/US2860040A/en not_active Expired - Lifetime
-
1956
- 1956-04-04 GB GB10289/56A patent/GB789857A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3505367A (en) * | 1961-02-14 | 1970-04-07 | Henri Brunel | Process for purifying raw sulfonates |
Also Published As
Publication number | Publication date |
---|---|
US2860040A (en) | 1958-11-11 |
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