GB784944A - Improvements in or relating to stable petroleum distillate fuels - Google Patents

Improvements in or relating to stable petroleum distillate fuels

Info

Publication number
GB784944A
GB784944A GB34326/54A GB3432654A GB784944A GB 784944 A GB784944 A GB 784944A GB 34326/54 A GB34326/54 A GB 34326/54A GB 3432654 A GB3432654 A GB 3432654A GB 784944 A GB784944 A GB 784944A
Authority
GB
United Kingdom
Prior art keywords
oil
alkyl
hydrocarbon
per cent
radical
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
GB34326/54A
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.)
Standard Oil Co
Original Assignee
Standard Oil Co
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 Standard Oil Co filed Critical Standard Oil Co
Publication of GB784944A publication Critical patent/GB784944A/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
    • C10L1/143Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
    • 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
    • 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
    • C10L1/234Macromolecular compounds
    • C10L1/238Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/2383Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
    • 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
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2691Compounds of uncertain formula; reaction of organic compounds (hydrocarbons acids, esters) with Px Sy, Px Sy Halz or sulfur and phosphorus containing compounds

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)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Abstract

A petroleum fuel oil composition contains 0.001 to 0.1 per cent of a neutralized reaction product of a phosphorus sulphide and a hydrocarbon and 0.001 to 0.1 per cent of at least one N-alkyl alkylene polyamine containing 6 to 30 carbon atoms in the N-alkyl radical, which may be substituted, and having at least one primary amino nitrogen atom, or an aliphatic carboxylic salt of such a compound. The petroleum oil may be an internal combustion engine fuel, a furnace oil, burner oil or heater oil, a kerosene, a jet fuel, or a residual fuel oil. A particular fuel mentioned comprises at least 10 per cent cracked oil boiling between 350 DEG and 750 DEG F. blended with virgin oil. The oil may first be treated by caustic alkali washing, acid treatment, Doctor sweetening, or by clay treatment. Products obtained by reacting a phosphorus sulphide with a hydrocarbon at 200 DEG F. to 600 DEG F., using 1 to 50 per cent by weight of the phosphorus sulphide, may be used. The hydrocarbons so treated may be mono-olefin hydrocarbon polymers, such as polymers of propylene, butylenes and amylenes, or copolymers of iso-mono-olefins and mono-olefins, preferably having molecular weights between 150 and 50,000; paraffinic hydrocarbons such as bright stock residuums, lubricating oil distillates, petrolatums or paraffin waxes; high molecular weight olefinic hydrocarbons, such as cetene, cerotene, melene and mixed high molecular weight alkenes obtained by cracking petroleum oils; olefins obtained by dehydrogenation of paraffins, or dehalogenation of long chain alkyl halides, or by the synthol process; aromatic hydrocarbons, such as benzene, naphthalene, anthracene, toluene and diphenyl, and alkylated aromatic hydrocarbons, such as an alkyl benzene having at least one alkyl group of at least four carbon atoms. The phosphorus sulphide may be P2S5, P2S3, P4S3 or P4S7. The phosphorus sulphide-hydrocarbon reaction product has at least 1 per cent of its acidity neutralized by treatment with a hydroxide, carbonate, sulphide or oxide of an alkaline earth metal or alkali metal, or with ammonia or an amine. The polyamino compound may have the formula: <FORM:0784944/III/1> where R is an alkyl or substituted alkyl (i.e. by hydroxy, carboxy, nitro or halo groups) radical having 6 to 30 carbon atoms; R1 is hydrogen or an aliphatic hydrocarbon radical; R11 is hydrogen, an alkylene primary amino radical (i.e.-(CH2)xNH2, where x is 1 to 10), or a poly alkylene polyamino radical containing a primary amino nitrogen atom; m is 1 to 10; and n is 0 to 10. Examples of polyamino compounds are N-octyl-ethylene diamine, N-dodecyl diethylene triamine, N-cetyl propylene diamine, N-octadecyl triethylene tetramine, N-hydroxyl dodecyl diethylene triamine, N-chloro-decylethylene diamine, N-bromo-octyl ethylene diamine, and "Duomeens" (Registered Trade Mark) which have the formula RNHCH2 CH2CH2NH2 where R is derived from coconut fatty acid, tallow fatty acid, lauric acid or soya fatty acid. The salts used are those of the polyamino compounds with aliphatic carboxylic acids having 6 to 20 carbon atoms, e.g. hexanoic, nonanoic, lauric, stearic, oleic, linoleic, linolenic and palmitic acids. The composition preferably contains both a polyamino compound and a salt thereof, with the phosphorus sulphide-hydrocarbon reaction product. A concentrated solution of the additives in a hydrocarbon oil may be prepared and then added to the oil to obtain the final composition. The composition may include surface active agents such as di-alkyl sodium sulphosuccinate, sodium cetyl sulphate, petroleum sulphonates, cetyl pyridinium chloride, octadecylamine acetate, and sodium mahogany soap.
GB34326/54A 1953-11-30 1954-11-26 Improvements in or relating to stable petroleum distillate fuels Expired GB784944A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US784944XA 1953-11-30 1953-11-30

Publications (1)

Publication Number Publication Date
GB784944A true GB784944A (en) 1957-10-23

Family

ID=22144361

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34326/54A Expired GB784944A (en) 1953-11-30 1954-11-26 Improvements in or relating to stable petroleum distillate fuels

Country Status (1)

Country Link
GB (1) GB784944A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357170A2 (en) * 2002-04-24 2003-10-29 Ethyl Corporation Friction modifier additives for fuel compositions and methods of use thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357170A2 (en) * 2002-04-24 2003-10-29 Ethyl Corporation Friction modifier additives for fuel compositions and methods of use thereof
EP1357170A3 (en) * 2002-04-24 2004-09-08 Ethyl Corporation Friction modifier additives for fuel compositions and methods of use thereof

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