GB911491A - Scavenger-free gasoline - Google Patents

Scavenger-free gasoline

Info

Publication number
GB911491A
GB911491A GB2169460A GB2169460A GB911491A GB 911491 A GB911491 A GB 911491A GB 2169460 A GB2169460 A GB 2169460A GB 2169460 A GB2169460 A GB 2169460A GB 911491 A GB911491 A GB 911491A
Authority
GB
United Kingdom
Prior art keywords
acid
lead
phosphate
butyl
octane number
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
GB2169460A
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.)
Ethyl Corp
Original Assignee
Ethyl Corp
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 Ethyl Corp filed Critical Ethyl Corp
Publication of GB911491A publication Critical patent/GB911491A/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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/10Use of additives to fuels or fires for particular purposes for improving the octane number
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

A gasoline composition contains from 1,5-4,3 grams of lead per U.S. gallon as an alkyl lead anti-knock agent, a gasoline soluble organic phosphorus compound present in amount such that the phosphorus to lead atom ratio is from 0,4:3 to 4:3 and an acidic compound, esters or aldehydes present in an amount ranging from 0,05 to 5% by volume based on the fuel, the base fuel containing from 10 to 60% by volume of aromatic hydrocarbons with the balance being non-aromatic hydrocarbons and having a nominal octane number of at least 90, the motor octane number being not more than 12 octane numbers less than its research octane number. The alkyl lead compound may be tetramethyl lead ethyltrimethyl lead, diethyldimethyl lead, methyltriethyl lead, tetrapropyl lead, tetraisopropyl lead, ethyltributyl lead or tetraamyl lead, the preferred compound being tetraethyl lead. The phosphorus compound may be triethyl phosphate, tributyl phosphate, tributylphosphite, tri-(2-ethylhexyl) phosphate, tris-(2-butoxyethyl) phosphate, tri-(2-chloroethyl) phosphate, tri-(b -chloropropyl) thionophosphate, triisopropylthionophosphate, tricyclohexylphosphite, triphenylphosphite, triphenylphosphate, tricrestylphosphate, cresyldiphenylphosphate, phenyldicresylphosphate, dioctylphenylphosphate, trimethylphosphate, phenyldimethylphosphate, cresyldimethylphosphate, xylyldimethylphosphate, diethylbutylphosphonate, bis-(2-chloroethyl) vinylphosphonate, S,S-di-butyl phenylphosphonodithioate, ditolychloromethyl-phosphonate, tris-(dimethylamido) phosphate, dixylylphorphoramidate, tributyl phosphine oxide or the corresponding phosphinates, phosphonites, thiophosphinates, phosphine oxides or phosphine sulphides. The reaction products of phosphorus sulphide with various organic substances may also be used. Suitable acidic compounds are monocarboxylic acids containing from 1 to 30 carbon atoms per molecule and containing no more than 3 oxygen atoms per molecule. A tertiary aliphatic hydrocarbon carbon ester or an anhyride of such an acid or an aldehyde may be used instead. Examples of suitable compounds are isobutyraldehyde, 2-ethylhexanoic acid, benzoic acid, tertiary butyl acetate, tertiary butyl-2-ethylhexanoate, tertiary-butylbenzoate, cyclohexane carboxylic acid, hexanoic acid, tertiarybutyl propionate, tertiary-amyl acetate, isobutyric anhydride, n-butyric anhydride, propionic anhydride, acetic anhydride, n-butyaldehyde, benzaldehyde, cumic acid, (neopentyl tertiarybutyl)- methylacetic acid, capric acid, lauric acid, ethoxyacetic acid, methoxy-acetic acid, 4-ketostearic acid, levulinic acid, 2-ethyl-hexaldehyde, paraldehyde, propionaldehyde, cinnamic acid, phenylacetic acid, di-(neopentyl)-acetic acid, 4-methylvaleric acid, 2-ethylbutyric acid, behenic acid, oleic acid, stearic acid, palmitic acid, myristic acid, pelargonic acid, heptanoic acid, caproic acid, propionic acid, acetic acid, and formic acid. The composition may also contain an aromatic amine such as methylaniline or a methyl toluidine or methyl xylidine or mixtures thereof; many other examples of suitable amines are given. Organometallic compounds of manganese, nickel, iron or cobalt may also be included. Other optional additives include anti-oxidants, e.g. N,N1-di-sec-butyl-p-phenylediamine, p-N-butyl-aminophenol, 4-methyl-2, 6-di-tert-butyl phenol, 2,6-di-tert-butyl phenol), metal deactivators (e.g. N,N1-disalicylidene-1,2-diaminopropane. The base fuel must contain from 10-60% of aromatics, the balance being saturates, olefines, naphthenes or combinations of these. The aromatic components may be catalytic reformates; the olefins may be formed by thermal cracking, catalytic cracking or polymerization; the saturated components comprise paraffins and naphthenes and may be straight-run gasolines, alkylates or isomerizates. The base fuel must have a nominal octane number of at least 90. Nominal octane number is defined as the octane number of the gasoline when it contains 3cc. of tetraethyl lead per U.S. gallon.
GB2169460A 1959-06-26 1960-06-21 Scavenger-free gasoline Expired GB911491A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US82302059A 1959-06-26 1959-06-26

Publications (1)

Publication Number Publication Date
GB911491A true GB911491A (en) 1962-11-28

Family

ID=25237576

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2169460A Expired GB911491A (en) 1959-06-26 1960-06-21 Scavenger-free gasoline

Country Status (1)

Country Link
GB (1) GB911491A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998001516A1 (en) * 1996-07-05 1998-01-15 Shell Internationale Research Maatschappij B.V. Fuel oil compositions
WO2003002696A1 (en) * 2001-05-12 2003-01-09 Aae Technologies International Plc Fuel composition
EP1650289A1 (en) * 2004-10-22 2006-04-26 Petroleo Brasileiro S.A. - PETROBAS Aviation gasoline formulation
WO2008076759A1 (en) * 2006-12-14 2008-06-26 Shell Oil Company Fuel composition and its use
EP2014745A1 (en) * 2007-07-10 2009-01-14 Afton Chemical Corporation Fuel composition comprising a nitrogen-containing compound
US7879775B2 (en) 2006-07-14 2011-02-01 Afton Chemical Corporation Lubricant compositions
US7902133B2 (en) 2006-07-14 2011-03-08 Afton Chemical Corporation Lubricant composition
US7906465B2 (en) 2006-07-14 2011-03-15 Afton Chemical Corp. Lubricant compositions
US8003584B2 (en) 2006-07-14 2011-08-23 Afton Chemical Corporation Lubricant compositions
US8715376B2 (en) 2009-04-09 2014-05-06 Shell Oil Company Fuel composition and its use

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6402797B1 (en) 1996-05-07 2002-06-11 Shell Oil Company Fuel oil compositions
WO1998001516A1 (en) * 1996-07-05 1998-01-15 Shell Internationale Research Maatschappij B.V. Fuel oil compositions
WO2003002696A1 (en) * 2001-05-12 2003-01-09 Aae Technologies International Plc Fuel composition
US7351268B2 (en) 2001-05-12 2008-04-01 Aae Technologies International Plc Fuel composition
EP1650289A1 (en) * 2004-10-22 2006-04-26 Petroleo Brasileiro S.A. - PETROBAS Aviation gasoline formulation
US7906465B2 (en) 2006-07-14 2011-03-15 Afton Chemical Corp. Lubricant compositions
US7879775B2 (en) 2006-07-14 2011-02-01 Afton Chemical Corporation Lubricant compositions
US7902133B2 (en) 2006-07-14 2011-03-08 Afton Chemical Corporation Lubricant composition
US8003584B2 (en) 2006-07-14 2011-08-23 Afton Chemical Corporation Lubricant compositions
WO2008076759A1 (en) * 2006-12-14 2008-06-26 Shell Oil Company Fuel composition and its use
US7976591B2 (en) 2006-12-14 2011-07-12 Shell Oil Company Fuel composition and its use
EP2014745A1 (en) * 2007-07-10 2009-01-14 Afton Chemical Corporation Fuel composition comprising a nitrogen-containing compound
US8715373B2 (en) 2007-07-10 2014-05-06 Afton Chemical Corporation Fuel composition comprising a nitrogen-containing compound
US8734540B2 (en) 2007-07-10 2014-05-27 Afton Chemical Corporation Fuel composition comprising a nitrogen-containing compound
US8715376B2 (en) 2009-04-09 2014-05-06 Shell Oil Company Fuel composition and its use

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