NO750823L - - Google Patents

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Publication number
NO750823L
NO750823L NO750823A NO750823A NO750823L NO 750823 L NO750823 L NO 750823L NO 750823 A NO750823 A NO 750823A NO 750823 A NO750823 A NO 750823A NO 750823 L NO750823 L NO 750823L
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NO
Norway
Prior art keywords
ester
acid
fatty acid
esters
alcohol
Prior art date
Application number
NO750823A
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Norwegian (no)
Inventor
M Lachat
Original Assignee
Autol Ag
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Publication of NO750823L publication Critical patent/NO750823L/no

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    • 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
    • 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
    • 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
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • 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
    • C10L10/02Use of additives to fuels or fires for particular purposes for reducing smoke development
    • 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
    • C10L10/06Use of additives to fuels or fires for particular purposes for facilitating soot removal
    • 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
    • C10L1/16Hydrocarbons
    • C10L1/1616Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
    • 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
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • 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

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  • 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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Description

Ved drift av forbrenningsmotorer oppstår det ved During the operation of internal combustion engines, there is

mange driftstilstander som følge av ufullstendig forbrenning mangler som: Korrosjon og slitasje på grunn av sure forbrennings-produkter; many operating conditions resulting from incomplete combustion are missing such as: Corrosion and wear due to acidic combustion products;

rester i brennkammeret og i utslippsveiene; residues in the combustion chamber and in the discharge paths;

skadelige stoffer som CO og uforbrente hydrokarboner i avgassene. harmful substances such as CO and unburned hydrocarbons in the exhaust gases.

Disse uungåelige fenomener er spesielt alvorlige ved'motorer som kjører i underkjølt tilstand3slik dette er tilfelle over korte strekninger. These unavoidable phenomena are particularly serious in the case of engines running in a subcooled state3, as is the case over short distances.

I tillegg til de nevnte mangler slik de oppstår på grunn av ufullstendig . forbrenning, kommer det ved forgassermot-orer forsmussing utenifra i innsugningssystemet og gjennom veiv-husluftningen. Disse forurensninger kan i sterk grad forstyrre dannelsen av en riktig drivstoffblanding, noe som fører til en forsterkning av de ovenfor angitte mangler. Fremfor alt kan inn-holdet av giftige CO i avgassene stige over den tillatte verdi. In addition to the aforementioned deficiencies as they arise due to incompleteness. combustion, in the case of carbureted engines, contamination comes from the outside in the intake system and through the crankcase ventilation. These contaminants can greatly interfere with the formation of a proper fuel mixture, leading to an amplification of the above-mentioned deficiencies. Above all, the content of toxic CO in the exhaust gases can rise above the permitted value.

Man forsøker å tilsidesette de ovenfor angitte mangler ved tilsetning av forskjellige tilsetningsstoffer til driv-stoffene. Et slikt tilsetningsstoff renser innsugningssystemet kontinuerlig for ikke eller tungt fordampende forurensninger slik som gummi, harpikser, smøremiddelande ler, skitt og ligenende, og • sikrer således dannelsen av en riktig drivstoffblanding. Like-ledes oppløses forbrenningsrester i brennkammeret og i utslippsveiene og beskytter materialene.for korrosjon. Attempts are made to override the above-mentioned shortcomings by adding various additives to the propellants. Such an additive continuously cleans the intake system of non- or heavily evaporating contaminants such as rubber, resins, lubricant clay, dirt and the like, and • thus ensures the formation of a correct fuel mixture. In the same way, combustion residues dissolve in the combustion chamber and in the discharge paths and protect the materials from corrosion.

Man har fastslått at tilsetning av et slikt tilsetningsstoff gir følgende fordeler: Beskyttelse av materialene for korrosjon; It has been established that the addition of such an additive provides the following advantages: Protection of the materials from corrosion;

anvendelsesmuligheter for drivstoffer med lavere application possibilities for fuels with lower

oktantall i Ottomotorer; octane number in Otto engines;

riktig dannelse av drivstoffblanding ved renhold av innsugningssystemet; correct formation of fuel mixture when cleaning the intake system;

reduksjon av skadelige stoffer i avgassene, slik som CO og uforbrente hydrokarboner; reduction of harmful substances in the exhaust gases, such as CO and unburned hydrocarbons;

renhold av brennkammeret og utslippsveiene for for-ta rennings rester; cleaning of the combustion chamber and the discharge paths to remove runoff residues;

forbedring av forbrenningen ved motordrivstoffer. improvement of the combustion of motor fuels.

Som tils-oningsstoffer er det allerede foreslått tall-rike kombinasjoner av antikorrosivt og rensende virkende sub-stanser. Det dreier seg derved hovédsakelig om kombinasjoner av korrosjohsbeskyttelsesmidler og også utvalgte detergentier med oppløsningsmidler slik som terpentinolj er, kamferoljer, alkoholr er, ketoner, estere og halogenhydrokarboner. I den senere tid er det som spesielt virksomt middel foreslått et additiv bestående av polyalkoholfettsyreestere, dvs. frie fettsyrer med minst 12 C-atomer, alifatiske fettsyrer slik som kalsiumfenylstearat. Videre er det foreslått i dette additiv i stedet for alifatiske fettsyreestere å anvende estere av fenol og dennes homologer eller fettsyreestere med en hydroksy- eller alkoksygruppe i fettsyredelen eller i alkoholdelen eller i begge, samt blandinger av disse estere. Numerous combinations of anticorrosive and purifying active substances have already been proposed as additives. This mainly involves combinations of corrosion protection agents and also selected detergents with solvents such as turpentine oil, camphor oils, alcohols, ketones, esters and halogenated hydrocarbons. In recent times, an additive consisting of polyalcohol fatty acid esters, i.e. free fatty acids with at least 12 C atoms, aliphatic fatty acids such as calcium phenylstearate, has been proposed as a particularly effective agent. Furthermore, it is proposed in this additive instead of aliphatic fatty acid esters to use esters of phenol and its homologues or fatty acid esters with a hydroxy or alkoxy group in the fatty acid part or in the alcohol part or in both, as well as mixtures of these esters.

Drivmiddeltilsetningsstoffene ifølge oppfinnelsen erkarakterisert vedat de som bærerkomponent inneholder minst en primær eller sekundær enverdig alkohol og/eller ketoalkohol. The fuel additives according to the invention are characterized in that they contain at least one primary or secondary monohydric alcohol and/or keto alcohol as a carrier component.

Et spesielt foretrukket tilsetningsmiddel for drivstoffer ifølge oppfinnelsen inneholder A particularly preferred additive for fuels according to the invention contains

a) et basisk kondensasjonsprodukt av 1 mol av et poly-etanolamin og minst 1 og maksimalt 2 mol av en fettsyre med minst a) a basic condensation product of 1 mol of a polyethanolamine and at least 1 and at most 2 mol of a fatty acid with at least

10 karbonatomer eller en ekvivalent mengde av en blanding av slike fettsyrer, b) en ester som ikke inneholder basiske grupper, hvilken ester stammer fra en eventuelt med hydroksy- eller alkoksygrupper substituert fettsyre, en aromatisk eller hydroaromatisk syre henholdsvis naftensyre eller en blanding av slike estere, hvilke estere ikke inneholder basiske -grupper, c) en eller flere mineraloljeraffinater med en viskosi-tet på minst 1,6° E/20°C og maksimalt 15° E/50°C og d) som bærerkomponent minst en primær eller sekundær en- 10 carbon atoms or an equivalent amount of a mixture of such fatty acids, b) an ester that does not contain basic groups, which ester originates from a fatty acid optionally substituted with hydroxy or alkoxy groups, an aromatic or hydroaromatic acid or naphthenic acid or a mixture of such esters , which esters do not contain basic groups, c) one or more mineral oil raffinates with a viscosity of at least 1.6° E/20°C and a maximum of 15° E/50°C and d) as carrier component at least one primary or secondary one-

verdig alkohol og/eller ketoalkohol. worthy alcohol and/or keto alcohol.

Som bærerkomponent foretrekkes primære eller sekundære enverdige alkoholer med opptil 10 karbonatomer, spesielt opptil 5 karbonatomer, slik som f.eks. propanoler og butanoler, spesielt isobutanol, men også metanol, isooktanol, Isononanol, dekanol osv., samt de primære eller sekundære enverdige keto-alkoholer, spesielt diacetonalkohol. °E betyr °Engler. Komponentene a) og b) anvendes vanligvis i mengder på opptil 50 vekt-% komponenten c) oftest i mengder fra 10 til 15%, ved tilsetningsstoffer for dieseldrivstoffer også i mengder opptil 80%. Bærerkomponenten utgjør vanligvis ca. 50% av tilsteningsstoffet, kan imidlertid også foreligge i mengder opptil ca. 80$. Primary or secondary monohydric alcohols with up to 10 carbon atoms, especially up to 5 carbon atoms, such as e.g. propanols and butanols, especially isobutanol, but also methanol, isooctanol, isononanol, decanol, etc., as well as the primary or secondary monovalent keto alcohols, especially diacetone alcohol. °E means °Angels. Components a) and b) are usually used in amounts of up to 50% by weight, component c) most often in amounts from 10 to 15%, with additives for diesel fuels also in amounts up to 80%. The carrier component usually amounts to approx. 50% of the calcifying substance, however, can also be present in amounts of up to approx. 80$.

Til fremstilling av komponenten a) kan man på i og for seg kjent måte oppvarme f. eks. 1 mol trietanolamin med 1-. mol av en fettsyre med minst 10 karbonatomer, f.eks. oljesyre, i en til tre timer til temperaturer på over 130°C. For å oppnå lyse kondensasjonsprodukter er det fordelaktig å gjennomføre reaksjonen i beholdere av glass, porselen eller korrosjonsfaste stål, det kan også være av.nytte å gjennomføre reaksjonen i vakuum under tilsetning av metalldesaktivatorer, slik som f.eks. en Schiff'sk base av salicylaldehyd. Etter fullstendig avdestilla-sjon av vann og avkjøling oppnår man ved anvendelse av oljesyre et lysegult til lett brunlig farget kondensasjonsprodukt som be-står overveiende av monooljesyreestren av trietanolamin. Hvis man i stedet for 1 mol oljesyre 2 mol av denne syre oppstår overveiende trietanolamindioljesyreester. De to nevnte kondensasjonsprodukter er lett oppløselige i de fleste oppløsningsmidler og i de mineraloljeraffinater som skal anvendes. For the production of component a), one can heat up in a manner known per se, e.g. 1 mole of triethanolamine with 1-. moles of a fatty acid with at least 10 carbon atoms, e.g. oleic acid, for one to three hours to temperatures above 130°C. In order to obtain bright condensation products, it is advantageous to carry out the reaction in containers made of glass, porcelain or corrosion-resistant steel, it can also be useful to carry out the reaction in a vacuum with the addition of metal deactivators, such as e.g. a Schiff's base of salicylaldehyde. After complete distillation of water and cooling, a pale yellow to slightly brownish colored condensation product is obtained by using oleic acid, which consists predominantly of the monooleic acid ester of triethanolamine. If, instead of 1 mol of oleic acid, 2 mol of this acid is used, predominantly triethanolamine diol ester is produced. The two condensation products mentioned are easily soluble in most solvents and in the mineral oil raffinates to be used.

I stedet for kondensasjonsproduktet av trietanolamin og en fettsyre med minst 10 karbonatomer kan man også anvende et produkt som oppnås ved analogkondensasjon av 1 mol dietanolamin med 1 mol av en fettsyre med minst 10 karbonatomer 'henholdsvis en blanding av slike fettsyrer. Hvis man som fettsyre anvender teknisk oljesyre oppnår man som reaksjonsprodukt overveiene monooljesyreestren av dietanolamin. Instead of the condensation product of triethanolamine and a fatty acid with at least 10 carbon atoms, a product obtained by analog condensation of 1 mol of diethanolamine with 1 mol of a fatty acid with at least 10 carbon atoms can also be used, respectively a mixture of such fatty acids. If technical oleic acid is used as the fatty acid, the reaction product is predominantly the monooleic acid ester of diethanolamine.

Som esterkomponenten b) egner seg spesielt alle til-svarende og i hydrokarboner oppløselige høyere kokende estere eller en blanding av estere, fortrinnsvis imidlertid slike med en begynnende koking på over 150°C, slik som f.eks. laurinsyre-etylester, smørsyreisooctylester3eddiksyreoleylester3 benzo-syreetylester3naftenisopropylester og cykloheksankarbonsyre-metylester. As the ester component b), all corresponding and hydrocarbon-soluble higher-boiling esters or a mixture of esters are particularly suitable, preferably, however, those with an initial boiling of over 150°C, such as e.g. lauric acid ethyl ester, butyric acid isooctyl ester 3 acetic oleyl ester 3 benzoic acid ethyl ester 3 naphthenic isopropyl ester and cyclohexanecarboxylic acid methyl ester.

Som ester komponent b) har dog estere av fenol og As ester component b) however has esters of phenol and

sine homologer og fettsyreestre der enten alkoholdelen eller fettsyredelen eller begge disse bærer en hydroksy- eller alkoksygruppe, eller blanding av slike' estre, vist seg spesielt virk-somme. Som estre av ^enol og dennes homologer skal f.eks. nevnes kresylacetat3xylenacetat, fenylnaftenat, kresylnaftenat eller kresylester av cykloheksankarbonsyre. Fettsyreestre som bærer en hydroksy- eller alkoksygruppe er f.eks. metoksybutylacetat, metoksyeddiksyreetylester,metoksybutylestren av metoksyeddik-syre, melkesyrecetylester3laurinsyremonoester av metylglykol, glykonmonooleat eller' blandinger derav. their homologues and fatty acid esters where either the alcohol part or the fatty acid part or both of these carry a hydroxy or alkoxy group, or mixtures of such esters, have proven particularly effective. As esters of ^enol and its homologues, e.g. mention is made of cresyl acetate-xylene acetate, phenyl naphthenate, cresyl naphthenate or cresyl ester of cyclohexanecarboxylic acid. Fatty acid esters bearing a hydroxy or alkoxy group are e.g. methoxybutyl acetate, methoxyacetic acid ethyl ester, methoxybutyl ester of methoxyacetic acid, lactic acid cetyl ester 3 lauric acid monoester of methyl glycol, glycone monooleate or' mixtures thereof.

Man kan oppløse komponentene a) og b) i vilkårlig rekkefølge i komponenten c), bærerkomponenten kan tilsettes på Components a) and b) can be dissolved in any order in component c), the carrier component can be added on

et hvilken som helst tidspunkt. any time.

Ved motorførsøk har det vist seg at allerede små mengder av de enkelte bestanddeler i tilsetningsstoffet utøver en optimal virkning på et vanlig dri-vstoff. Vanligvis er det tilstrekkelig med 0,005 til 1 volum-%, fortrinnsvis 0,02 til 0,5 volum-%, beregnet på motordrivstoffet. In engine tests, it has been shown that even small amounts of the individual components in the additive exert an optimal effect on a normal fuel. Usually 0.005 to 1% by volume, preferably 0.02 to 0.5% by volume, calculated on the motor fuel is sufficient.

Den angjeldende mengde av de i tilsetningsmidlet foreliggende enkeltkomponenter retter seg vidtgående etter den ønskede konsentrasjon av enkeltkomponentene i motordrivstoffet og etter mengden av tilsetningsmidlet som skal tilføres drivstof-fet. The relevant quantity of the individual components present in the additive largely depends on the desired concentration of the individual components in the motor fuel and on the amount of the additive to be added to the fuel oil.

Tilsetningsmidlet kan i tillegg til mineraloljeraffinater også inneholde syntetiske alifatiske hydrokarboner slik som "kogasin" og også syntetiske eller naturlige aromatiske hydrokarboner slik som alkylbenzoler. Tilsetningsmidlene kan videre inneholde andre stoffer slik som f.eks. korrosjonsinhi-bitorer, tenningsakselatorer, oktantallforbedrere, antioksydan-ter, høytryktilsetningsstoffer, forbrenningskatalysatorer og lignende, alt sammen stoffer som vanligvis tilsettes til drivstoffer. In addition to mineral oil raffinates, the additive may also contain synthetic aliphatic hydrocarbons such as "cogasine" and also synthetic or natural aromatic hydrocarbons such as alkylbenzenes. The additives may also contain other substances such as e.g. corrosion inhibitors, ignition accelerators, octane number improvers, antioxidants, high pressure additives, combustion catalysts and the like, all substances which are usually added to fuels.

Claims (2)

1. Drivstofftilsetningsmiddel for forbrenningsmotorer,karakterisert vedat det som bærerkomponent inneholder minst en primær eller sekundær enverdig alkohol og/ eller ketoalkohol.1. Fuel additive for internal combustion engines, characterized in that it contains as carrier component at least one primary or secondary monohydric alcohol and/or keto alcohol. 2. Drivstofftilsetningsmiddel ifølge krav 1,karakterisert vedat det inneholder a) et basi " kondensasjonsprodukt av 1 mol av et poly-etanolamin og minst 1 og maksimalt 2 mol av en fettsyre med minst 10 karbonatomer eller en ekvivalent mengde' av en blanding av slike fettsyrer, b) et ester som ikke inneholder basiske grupper, hvilken ester stammer fra en eventuelt med hydroksy- eller alkoksygrupper substituert fettsyre, en ester av en aromatisk eller hydroaromatisk .syre henholdsvis naftensyre eller en blanding av slike estere, hvilken ester ikke inneholder basiske grupper, c) en eller flere mineraloljeraffinater med en viskosi-tet på'minst 1,6° E/20°C og maksimalt 15° E/50°C og d) minst en primær eller sekundær enverdig alkohol og/ eller ketoalkohol som bærerkomponent.2. Fuel additive according to claim 1, characterized in that it contains a) a basic condensation product of 1 mol of a polyethanolamine and at least 1 and at most 2 mol of a fatty acid with at least 10 carbon atoms or an equivalent amount of a mixture of such fatty acids , b) an ester that does not contain basic groups, which ester originates from a fatty acid optionally substituted with hydroxy or alkoxy groups, an ester of an aromatic or hydroaromatic acid or naphthenic acid or a mixture of such esters, which ester does not contain basic groups, c) one or more mineral oil raffinates with a viscosity of at least 1.6° E/20°C and a maximum of 15° E/50°C and d) at least one primary or secondary monohydric alcohol and/or keto alcohol as carrier component.
NO750823A 1974-03-14 1975-03-11 NO750823L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH359074 1974-03-14
CH708074 1974-05-22

Publications (1)

Publication Number Publication Date
NO750823L true NO750823L (en) 1975-09-16

Family

ID=25693383

Family Applications (1)

Application Number Title Priority Date Filing Date
NO750823A NO750823L (en) 1974-03-14 1975-03-11

Country Status (12)

Country Link
JP (1) JPS50132007A (en)
BR (1) BR7501487A (en)
DD (1) DD116260A5 (en)
DE (1) DE2511249A1 (en)
DK (1) DK102675A (en)
FI (1) FI750728A (en)
FR (1) FR2273058A1 (en)
IT (1) IT1030334B (en)
LU (1) LU72045A1 (en)
NL (1) NL7503061A (en)
NO (1) NO750823L (en)
SE (1) SE7502830L (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4204481A (en) * 1979-02-02 1980-05-27 Ethyl Corporation Anti-wear additives in diesel fuels
ES2017030A6 (en) * 1989-07-26 1990-12-16 Lascaray Sa Additive compound for fuels intended for internal combustion engines
AU761457B2 (en) * 1998-01-12 2003-06-05 Deborah Wenzel An additive composition also used as a fuel composition comprising water soluble alcohols
GB2516862A (en) 2013-08-01 2015-02-11 M I Drilling Fluids Uk Ltd Quaternary ammonium compounds and gas hydrate inhibitor compositions

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Publication number Publication date
DE2511249A1 (en) 1975-09-25
SE7502830L (en) 1975-09-15
NL7503061A (en) 1975-09-16
DD116260A5 (en) 1975-11-12
DK102675A (en) 1975-09-15
FR2273058B1 (en) 1977-04-15
LU72045A1 (en) 1975-08-20
IT1030334B (en) 1979-03-30
FR2273058A1 (en) 1975-12-26
BR7501487A (en) 1975-12-16
JPS50132007A (en) 1975-10-18
FI750728A (en) 1975-09-15

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