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GB719776A - Diesel fuel - Google Patents

Diesel fuel

Info

Publication number
GB719776A
GB719776A GB30525/50A GB3052550A GB719776A GB 719776 A GB719776 A GB 719776A GB 30525/50 A GB30525/50 A GB 30525/50A GB 3052550 A GB3052550 A GB 3052550A GB 719776 A GB719776 A GB 719776A
Authority
GB
United Kingdom
Prior art keywords
lead
sulphonate
benzene
per cent
petroleum
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
GB30525/50A
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.)
California Research LLC
Original Assignee
California Research LLC
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 California Research LLC filed Critical California Research LLC
Publication of GB719776A publication Critical patent/GB719776A/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
    • C10L10/08Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
    • 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
    • C10L1/24Organic compounds containing sulfur, selenium and/or tellurium
    • 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
    • C10L10/04Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation

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)
  • Liquid Carbonaceous Fuels (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Lead sulphonates and naphthenates are employed as ingredients in fuel oil compositions (see Group III). Specification 674,765, [Group III], is referred to. Lead mahogany sulphonate.-Crude calcium mahogany sulphonate (50 per cent oil) is dissolved in a petroleum distillate (boiling range 185-290 DEG F.) and the solution is repeatedly washed with aqueous lead nitrate in the presence of ethyl alcohol with steam agitation. A small amount of litharge is added to neutralize any acidity and the petroleum distillate is distilled off, leaving a concentrate of lead mahogany sulphonate. Lead alkyl benzene sulphonate.-Benzene is alkylated with polypropylene (a C12-C15 olefin cut) and the alkylated benzene is sulphonated with concentrated sulphuric acid and then neutralized with sodium hydroxide. The sodium sulphonate is reacted with lead nitrate to obtain the lead sulphonate. Basic lead alkyl benzene sulphonate.-The alkyl benzene sulphonic acid prepared as above is reacted with a 100 per cent stoichiometric excess of litharge to obtain the basic lead salt. Lead naphthenate.-Petroleum gas oil is washed with aqueous caustic soda and the aqueous sodium naphthenate solution is treated with strong sulphuric acid to release the naphthenic acid. This is distilled and then treated with litharge. Lead naphthenate is extracted from the reaction mixture with Stoddard solvent.ALSO:A composition which, in spite of its sulphur content, causes little engine wear when employed as a fuel for diesel engines comprises a petroleum distillate boiling in the range of about 350-750 DEG F. and having an A.P.I. gravity above 20 DEG and a sulphur content above about 0.5 per cent. by weight, together with a minor proportion of an oil-soluble lead naphthenate, lead sulphonate and/or lead salt of a fatty acid, sufficient to give the composition a lead content of about 0.005-0.07 per cent. by weight. The sulphonic acids from which suitable lead sulphonates are prepared are preferably those having a molecular weight above about 400, for example sulphonic acids obtained by sulphonating white oils, petroleum lubricating oil fractions, higher boiling fractions of SO2 extracts of petroleum gas oils, and high boiling synthetic alkylated aromatic hydrocarbons, such as those formed by alkylating benzene with propylene polymers, butylene polymers or mixed propylene-butylene polymers. Lead salts of fatty acids mentioned are the oleate, palmitate, and stearate, and the soaps prepared from unrefined fats. In the examples, the normal or basic lead salt of naphthenic acids of molecular weight above about 225, or of sulphonic acids prepared by alkylating benzene with polypropylene (C12-C15 cut) and sulphonating the product, is added to the petroleum distillate. Specification 674,765 is referred to.
GB30525/50A 1949-12-28 1950-12-14 Diesel fuel Expired GB719776A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US135507A US2691572A (en) 1949-12-28 1949-12-28 High sulfur diesel fuel containing organic lead salts

Publications (1)

Publication Number Publication Date
GB719776A true GB719776A (en) 1954-12-08

Family

ID=22468414

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30525/50A Expired GB719776A (en) 1949-12-28 1950-12-14 Diesel fuel

Country Status (2)

Country Link
US (1) US2691572A (en)
GB (1) GB719776A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1034918B (en) * 1956-05-03 1958-07-24 Exxon Standard Sa Fuel for internal combustion engines working with carburettors and spark ignition

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2789892A (en) * 1952-10-22 1957-04-23 California Research Corp Diesel fuel composition
DE1077358B (en) * 1957-08-22 1960-03-10 Exxon Research Engineering Co Heating oil
BE581117A (en) * 1958-09-26
DE1545266B1 (en) * 1966-04-27 1969-10-16 Dasic Chemicals Ltd Compensation for heavy heating oils with a high sulfur content

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB599222A (en) * 1945-09-21 1948-03-08 Anglo Iranian Oil Co Ltd Improvements relating to motor fuels
US2045788A (en) * 1933-07-11 1936-06-30 Standard Oil Dev Co Fuel for high pressure liquid fuel injection engines
US2230642A (en) * 1938-08-13 1941-02-04 Standard Oil Dev Co Fuel oil
GB561328A (en) * 1941-07-05 1944-05-15 Standard Oil Dev Co Improvements relating to fuel oils
US2575003A (en) * 1948-07-03 1951-11-13 Shell Dev Fuel oil composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1034918B (en) * 1956-05-03 1958-07-24 Exxon Standard Sa Fuel for internal combustion engines working with carburettors and spark ignition

Also Published As

Publication number Publication date
US2691572A (en) 1954-10-12

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