GB816090A - Gasoline compositions - Google Patents

Gasoline compositions

Info

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
Application number
GB18826/57A
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.)
ExxonMobil Oil Corp
Original Assignee
Socony Mobil Oil Co Inc
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 Socony Mobil Oil Co Inc filed Critical Socony Mobil Oil Co Inc
Publication of GB816090A publication Critical patent/GB816090A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic 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.
GB18826/57A 1956-06-29 1957-06-14 Gasoline compositions Expired GB816090A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
FR1180709A (en) 1959-06-09
US2902353A (en) 1959-09-01

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