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DE1221845B - Diesel fuels - Google Patents

Diesel fuels

Info

Publication number
DE1221845B
DE1221845B DEJ21845A DEJ0021845A DE1221845B DE 1221845 B DE1221845 B DE 1221845B DE J21845 A DEJ21845 A DE J21845A DE J0021845 A DEJ0021845 A DE J0021845A DE 1221845 B DE1221845 B DE 1221845B
Authority
DE
Germany
Prior art keywords
wear
ooc
fuels
carbon atoms
diesel fuels
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.)
Pending
Application number
DEJ21845A
Other languages
German (de)
Inventor
Jean Larbre
Louis Pons
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.)
IFP Energies Nouvelles IFPEN
Original Assignee
IFP Energies Nouvelles IFPEN
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 IFP Energies Nouvelles IFPEN filed Critical IFP Energies Nouvelles IFPEN
Publication of DE1221845B publication Critical patent/DE1221845B/en
Pending 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • C10L1/1983Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyesters
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • C10L1/1985Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Fuel-Injection Apparatus (AREA)

Description

BUNDESREPUBLIK DEUTSCHLANDFEDERAL REPUBLIC OF GERMANY

DEUTSCHESGERMAN

PATENTAMTPATENT OFFICE

AUSLEGESCHRIFTEDITORIAL

Int. CL:Int. CL:

Nummer:
Aktenzeichen:
Anmeldetag:
Auslegetag:
Number:
File number:
Registration date:
Display day:

ClOlClOl

Deutsche KL: 46 a6 - 7German KL: 46 a6 - 7

J21845IVd/46a6
29. Mai 1962
28. Juli 1966
J21845IVd / 46a6
May 29, 1962
July 28, 1966

Die Abnutzung der Einspritzvorrichtungen von Dieselmotoren, die mit leichteren Kraftstoffen als Gasöl betrieben werden, wird immer problematischer. Dies gilt besonders für Motoren, die mit verschiedenen Kraftstoffen betrieben werden können, wie sie besonders in Entwicklungsländern benutzt werden, in denen die mit Benzin betriebenen Tourenwagen wenig verbreitet sind und in denen daher ein Überangebot an leichten Erdölfraktionen besteht.The wear and tear on the injectors of diesel engines using lighter fuels than Gas oil is becoming more and more problematic. This is especially true for engines that use different Fuels can be operated as they are used in developing countries in particular in which petrol-powered touring cars are not very common and in which there is therefore an oversupply consists of light petroleum fractions.

Es ist daher die Aufgabe der Erfindung, Dieselkraftstoff^ mit verminderter Abnutzung der Einspritzvorrichtungen aus leichten Brennstoffen oder Erdölfraktionen zu schaffen.It is therefore the object of the invention to provide diesel fuel ^ with reduced wear and tear on injectors from light fuels or petroleum fractions to accomplish.

Dies geschieht durch Zusatz von 0,01 bis 5 Gewichtsprozent eines Polyesters der Formel:This is done by adding 0.01 to 5 percent by weight of a polyester of the formula:

R1 - (- OOC - A - COO - B -)„ - OOC - A - COOR8 R 1 - (- OOC - A - COO - B -) "- OOC - A - COOR 8

in der A ein zweiwertiger aliphatischer, aromatischer oder naphthenischer Rest ist, der eventuell substituiert sein kann und 4 bis 20 Kohlenstoffatome enthält, B einen Alkylenrest mit 2 bis 20 Kohlenstoffatomen sowie R1 und R2 Alkylreste bedeuten und η eine ganze Zahl mindestens gleich 1 ist.in which A is a divalent aliphatic, aromatic or naphthenic radical which may be substituted and contains 4 to 20 carbon atoms, B is an alkylene radical with 2 to 20 carbon atoms and R 1 and R 2 are alkyl radicals and η is an integer at least equal to 1 .

Die folgenden Verbindungen können dazu verwendet werden:The following connections can be used for this:

DieselkraftstoffeDiesel fuels

Anmelder:Applicant:

Institut Frangais du Petrole des CarburantsInstitut Frangais du Petrole des Carburants

et Lubrifiants,et Lubrifiants,

Rueil-Malmaison, Seine-et-Oise (Frankreich)Rueil-Malmaison, Seine-et-Oise (France)

Vertreter:Representative:

Dr.-Ing. G. Riebling, Patentanwalt,Dr.-Ing. G. Riebling, patent attorney,

Lindau (Bodensee), Rennerle 10Lindau (Lake Constance), Rennerle 10

Als Erfinder benannt:Named as inventor:

Jean Larbre, Colombes, Seine;Jean Larbre, Colombes, Seine;

Louis Pons,Louis Pons,

Rueil-Malmaison, Seine-et-Oise (Frankreich)Rueil-Malmaison, Seine-et-Oise (France)

Beanspruchte Priorität:Claimed priority:

Frankreich vom 31. Mai 1961 (863 694)France of May 31, 1961 (863 694)

Mischpolyadipat aus Propylenglykol und Isodecanol, Mixed polyadipate from propylene glycol and isodecanol,

Mischpolyadipat aus Propylenglykol und Isododecanol, Mixed polyadipate from propylene glycol and isododecanol,

Mischpolysebacat aus Äthylenglykol und Isohexanol. Mixed polysebacate from ethylene glycol and isohexanol.

Diese Verbindungen werden vorteilhaft in einer Konzentration von 0,01 bis 5 und vorzugsweise von 0,05 bis 0,5 Gewichtsprozent verwendet.These compounds are advantageously used at a concentration of from 0.01 to 5, and preferably from 0.05 to 0.5 weight percent used.

Die Auflösung dieser Produkte kann durch ihre vorherige Verdünnung mittels aromatischer Kohlenwasserstoffe oder Kohlenwasserstoffgemischem'.teinem hohen Gehalt an Aromaten erleichtert ν erdsa.These products can be dissolved by diluting them beforehand using aromatic hydrocarbons or hydrocarbon mixtures with a high aromatic content, ν erdsa facilitates.

Die erfindungsgemäß verwendeten Polyester haben eine ihre Anwendungszeit überdauernde Wirkung, so daß die mechanischen Einspritzvorrichtungen mehrere Stunden ohne nennenswerte Abnützung verwendet werden können.The polyesters used in the present invention have an effect lasting their time of use, so that the mechanical injectors can be used for several hours without significant wear and tear.

Es sei noch bemerkt, daß bei Verwendung gleicher Mengen der üblichen Schmiermittel gleicher Viskosität keine vergleichbaren Ergebnisse erzielt werden können. Die Hauptmerkmale der Kraftstoffe und ihre Oktanzahlen werden durch den Zusatz dieser Produkte nicht verändert, und der Motor wird nicht verschmutzt.It should also be noted that when using the same amounts of the usual lubricants the same viscosity no comparable results can be achieved. The main characteristics of fuels and their octane numbers are not changed by the addition of these products, and the engine is not contaminated.

Einem auf einen Druck von 170 kg/cm2 eingestellten Einspritzer, dessen Nadel vorher in einem Kernreaktor bestrahlt wurde, wird mittels einer Kolbenpumpe Kraftstoff zugeführt. Die sich aus der Abnutzung der Nadel ergebenden Metallteilchen werden von dem Kraftstoff weggespült und sammeln sich auf einem Glasfrittefilter, durch das der Kraftstoff austritt. Aus der Messung der Radioaktivität des Filters schließt man auf die Menge der sich aus der Abnutzung der Nadel ergebenden Teilchen durch Vergleiche mit Teilen des gleichen Metalls, die der gleichen Bestrahlung unterworfen wurden und deren Gewicht bekannt ist.An injector set to a pressure of 170 kg / cm 2 , the needle of which was previously irradiated in a nuclear reactor, is supplied with fuel by means of a piston pump. The metal particles resulting from the wear of the needle are washed away by the fuel and collect on a glass frit filter through which the fuel exits. By measuring the radioactivity of the filter, the amount of particles resulting from the wear of the needle is inferred by comparing it with parts of the same metal which have been subjected to the same irradiation and whose weight is known.

Der verwendete Kraftstoff ist ein nicht äthyliertes Benzin mit einer Oktanzahl von 87, in dem ein Mischpolyadipat aus Propylenglykol und rohem Isodecanol aufgelöst wurde. Die letztgenannte Verbindung wurde durch Reaktion von 14,5 Mol Adipinsäure mit 12,9 Mol Propylenglykol und 5 Mol Isodecanol erhalten.The fuel used is a non-ethylated gasoline with an octane rating of 87, in which a mixed polyadipate was dissolved from propylene glycol and crude isodecanol. The latter connection was made obtained by reacting 14.5 moles of adipic acid with 12.9 moles of propylene glycol and 5 moles of isodecanol.

Auf Grund der erzielten Ergebnisse wurde die folgende Tabelle aufgestellt, die in Abhängigkeit von der in Gewichtsprozent ausgedrückten Konzentration des Zusatzes die entsprechenden Abnutzungswerte des Einspritzers bei 250C sowie bei 700C wiedergibt, wobei unter Abnutzung das Verhältnis der beobachteten Abnutzung zu der in Abwesenheit eines Zusatzmittels entstehenden Abnutzung steht, ausgedrückt durch die entsprechenden Gewichtsverluste.On the basis of the results obtained, the following table was drawn up which, depending on the concentration of the additive expressed in percent by weight, shows the corresponding wear values of the injector at 25 ° C. and at 70 ° C., with wear being the ratio of the wear observed to that in the absence wear resulting from an additive, expressed by the corresponding weight loss.

609 607/181609 607/181

Zusatzadditive Abnutzung bei einer TemperaturWear at a temperature αα 70° C70 ° C (in Gewichtsprozent)(in percent by weight) VOI
25° C
VOI
25 ° C
11
00 \ ' 1\ ' 1 0,50.5 0,010.01 0,750.75 0,400.40 0,020.02 0,500.50 0,250.25 0,050.05 0,320.32 0,150.15 0,10.1 0,250.25 0,070.07 0,20.2 0,200.20 - 0,50.5 0,110.11 - 0,850.85 0,080.08

Will man bei der Verwendung von Rizinusöl eine Verringerung der Abnutzung um 50% bei 25° C erzielen, so muß man eine ungefähr 50mal stärkere Konzentration, also eine l%ige verwenden.If it is desired for the use of castor oil, a reduction of wear by 50% at 25 ° C achieved, an about 50 times higher concentration, ie use a l% strength must be e.

Claims (1)

Patentanspruch:Claim: Dieselkraftstoffe aus leichteren Kraftstoffen oder Erdölfraktionen als Gasöl, gekennzeichnet durch einen Gehalt von 0,01 bis 5 Gewichtsprozent eines Polyesters der FormelDiesel fuels made from lighter fuels or petroleum fractions are labeled as gas oil by a content of 0.01 to 5 percent by weight of a polyester of the formula R1-(-OOC-A-COO-B-)?l-OOC-A-COOR2 R 1 - (- OOC-A-COO-B-) ? L -OOC-A-COOR 2 in der A ein zweiwertiger aliphatischer, aromatischer oder naphthenischer Rest ist, der eventuell substituiert sein kann und 4 bis 20 Kohlenstoffatome enthält, B einen Alkylenrest mit 2 bis 20 Kohlenstoffatomen und R1 und R2 Alkylreste bedeuten und η eine ganze Zahl mindestens gleich 1 ist.in which A is a divalent aliphatic, aromatic or naphthenic radical which can optionally be substituted and contains 4 to 20 carbon atoms, B is an alkylene radical having 2 to 20 carbon atoms and R 1 and R 2 are alkyl radicals and η is an integer at least equal to 1 . In Betracht gezogene Druckschriften:
USA.-Patentschrift Nr. 2 844 448.
Considered publications:
U.S. Patent No. 2,844,448.
609 607/181 7.66 © Bundesdruckerei Berlin609 607/181 7.66 © Bundesdruckerei Berlin
DEJ21845A 1961-05-31 1962-05-29 Diesel fuels Pending DE1221845B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR863694A FR1317217A (en) 1961-05-31 1961-05-31 Method of reducing wear in injection engines and fuel compositions for these engines

Publications (1)

Publication Number Publication Date
DE1221845B true DE1221845B (en) 1966-07-28

Family

ID=8756419

Family Applications (1)

Application Number Title Priority Date Filing Date
DEJ21845A Pending DE1221845B (en) 1961-05-31 1962-05-29 Diesel fuels

Country Status (4)

Country Link
DE (1) DE1221845B (en)
FR (1) FR1317217A (en)
GB (1) GB949707A (en)
OA (1) OA01604A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3916365A1 (en) * 1989-05-19 1990-11-22 Basf Ag FUEL COMPOSITIONS CONTAINING ALKOXYLATION PRODUCTS
US5466267A (en) * 1992-09-17 1995-11-14 Mobil Oil Corporation Oligomeric/polymeric multifunctional additives to improve the low-temperature properties of distillate fuels
US5538521A (en) * 1993-12-23 1996-07-23 Chevron Chemical Company Fuel compositions containing polyalkyl and poly(oxyalkylene)aromatic esters

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2844448A (en) * 1955-12-23 1958-07-22 Texas Co Fuels containing a deposit-control additive

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2844448A (en) * 1955-12-23 1958-07-22 Texas Co Fuels containing a deposit-control additive

Also Published As

Publication number Publication date
OA01604A (en) 1969-09-20
GB949707A (en) 1964-02-19
FR1317217A (en) 1963-02-08

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