GB816090A - Gasoline compositions - Google Patents
Gasoline compositionsInfo
- Publication number
- GB816090A GB816090A GB18826/57A GB1882657A GB816090A GB 816090 A GB816090 A GB 816090A GB 18826/57 A GB18826/57 A GB 18826/57A GB 1882657 A GB1882657 A GB 1882657A GB 816090 A GB816090 A GB 816090A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amine
- diamine
- per cent
- mono
- salt
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
- C10L1/2225—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A gasoline with improved anti-stalling characteristics contains 0.004-1.0 per cent, by weight, of a carboxylic acid salt of an hydroxy aliphatic amine, the amine being represented either by the formul RaN(R1OH)b where R is an aliphatic radical of from 1-20 carbon atoms (or is composed of a plurality of such radicals); R1 is a -CH2CH2- or -CH2-C(CH3)H- radical; a is 0 to 2 and b is 1 to 3, the sums of a and b always being 3, or by the formula <FORM:0816090/III/1> where R, R1 are defined above and a is 0 to 1; b is 1 to 2; the sum of a and b is 2, and n is 1 to 2. The carboxylic acid is preferably salicylic or naphthenic acid to give the single or double carboxylic acid aliphatic hydroxy amine salt but other suitable acids are those occurring in tall oil, castor oil, rape seed oil or from the oxidation of petroleum, acetic, propionic, butyric, valeric, caprylic, lauric, myristic, palmitic, stearic, oleic, linoleic, dimer of linoleic, hyenic and psyllic acids or benzoic, phthalic and other aromatic acids. The salt product may be a mono- or diacid salt of an aliphatic hydroxy diamine, or a mono- or di-aliphatic hydroxy amine salt of a dicarboxylic acid, or a mixture of such salts. The reaction may be carried out in a solvent medium, e.g. petroleum naphtha, which can be wholly or partially retained to form a concentrated solution of the salt for addition to the gasoline. Preparation of suitable amines is effected by the reaction of ethylene oxide or propylene oxide with amino compounds having at least one hydrogen atom attached to an amino nitrogen, including ammonia, primary and secondary aliphatic amines and diamines, for example (1) primary or secondary aliphatic monoamines, including methyl amine, propyl amine, butyl amine, tertiary butyl amine, di-butyl amine, cyclohexyl amine, octyl amine, di-octyl amine, tertiary octyl, primary amine, decyl amine, di-dodecyl amine, tetradecyl amine, hexadecyl amine, octadecyl amine, di-octadecyl amine, octadecenyl amine and dehydro-abietyl amine or mixtures of these amines; (2) diamines including ethylene diamine, where R is hydrogen, and the following where R is an aliphatic group: N - methyl - 1,3 - trimethylene diamine, N - ethyl - 1,3 - trimethylene diamine, N - hexyl - 1,3 - trimethylene diamine, N - octyl - 1,3 - trimethylene diamine, N - decyl - 1,3 - trimethyene diamine, N-dodecyl-1,3-trimethylene diamine, N - tetradecyl - 1,3 - trimethylene diamine, N - hexadecyl - 1,3 - trimethylene diamine, N - octadecyl - 1,3 - trimethylene diamine, N - octadecenyl - 1,3 - trimethylene diamine, N - dehydroabietyl - 1,3 - trimethylene diamine or mixtures of these diamines. Examples of the additives for various gasolines are triethanolamine oleate; mono- and disalicylate salts of the mixture of aliphatic hydroxy diamines containing (a) 2 per cent tetradecyl diamine, 24 per cent hexadecyldiamine, 28 per cent octadecyl diamine and 46 per cent octadecenyl diamine; mono- and dinaphthenate salts of the mixture of aliphatic hydroxy diamines as above; the mono-trichloro-acetate salt of the aliphatic hydroxy mono amines containing (6) 8 per cent octyl, 9 per cent decyl-, 47 per cent dodecyl-, 18 per cent tetradecyl-, 8 per cent hexadecyl-, 5 per cent octadecyl- and 5 per cent octadecenylamines; the mono-salicylate salt of the aliphatic hydroxy mono-amine containing mixture (b); the mono - naphthenate salt of N,N,N1,N1-tetrakis - (2 - hydroxy - propyl) - ethylene diamine; the mono- and di-naphthenate salt of the aliphatic hydroxy amine containing composition (b) above; the mono-glycolate salt of the aliphatic hydroxy diamine containing composition (a) above.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US594718A US2902353A (en) | 1956-06-29 | 1956-06-29 | Anti-stall gasoline |
Publications (1)
Publication Number | Publication Date |
---|---|
GB816090A true GB816090A (en) | 1959-07-08 |
Family
ID=24380087
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18826/57A Expired GB816090A (en) | 1956-06-29 | 1957-06-14 | Gasoline compositions |
Country Status (3)
Country | Link |
---|---|
US (1) | US2902353A (en) |
FR (1) | FR1180709A (en) |
GB (1) | GB816090A (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3055746A (en) * | 1959-05-07 | 1962-09-25 | Texaco Inc | Adducts of aliphatic monocarboxylic acids and aliphatic amines in gasoline |
BE597708A (en) * | 1959-12-01 | |||
US3115399A (en) * | 1960-08-01 | 1963-12-24 | Armour & Co | Fuel composition |
US3148039A (en) * | 1960-11-14 | 1964-09-08 | Texaco Inc | Anti-stalling motor fuel |
US3106461A (en) * | 1961-03-03 | 1963-10-08 | Texaco Inc | Anti-stalling motor fuel |
US3473902A (en) * | 1965-08-26 | 1969-10-21 | Texaco Inc | Fuel composition |
US3844731A (en) * | 1973-06-14 | 1974-10-29 | Texaco Inc | Motor fuel additive |
US3873278A (en) * | 1973-11-29 | 1975-03-25 | Du Pont | Gasoline |
US3894849A (en) * | 1973-11-29 | 1975-07-15 | Du Pont | Gasoline |
US5968211A (en) * | 1995-12-22 | 1999-10-19 | Exxon Research And Engineering Co. | Gasoline additive concentrate |
EP0829527A1 (en) | 1996-09-12 | 1998-03-18 | Exxon Research And Engineering Company | Additive concentrate for fuel compositions |
PE20030998A1 (en) * | 2002-02-12 | 2004-01-30 | Shell Int Research | GASOLINE COMPOSITIONS |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1990365A (en) * | 1932-03-21 | 1935-02-05 | Standard Oil Co | Top cylinder lubricant |
US2125448A (en) * | 1935-12-21 | 1938-08-02 | Joseph W Johnson | Fuel |
US2329251A (en) * | 1941-01-21 | 1943-09-14 | Universal Oil Prod Co | Treatment of gasoline |
US2667408A (en) * | 1949-10-05 | 1954-01-26 | Sinclair Refining Co | Prevention of rust |
US2706677A (en) * | 1950-06-28 | 1955-04-19 | Exxon Research Engineering Co | Amines and amides as anti-stalling additives |
GB701459A (en) * | 1951-01-09 | 1953-12-23 | Standard Oil Dev Co | Improvements in or relating to aviation turbo fuel |
US2840461A (en) * | 1954-12-06 | 1958-06-24 | Exxon Research Engineering Co | Dialkyl alkanol amines as anti-stalling additives |
US2843464A (en) * | 1956-04-06 | 1958-07-15 | Gulf Research Development Co | Non-stalling gasoline fuel compositions |
-
1956
- 1956-06-29 US US594718A patent/US2902353A/en not_active Expired - Lifetime
-
1957
- 1957-06-14 GB GB18826/57A patent/GB816090A/en not_active Expired
- 1957-06-28 FR FR1180709D patent/FR1180709A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1180709A (en) | 1959-06-09 |
US2902353A (en) | 1959-09-01 |
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