DE2327546A1 - METHOD OF LUBRICATING TWO-STROKE AND ROTARY LISTON ENGINES - Google Patents

METHOD OF LUBRICATING TWO-STROKE AND ROTARY LISTON ENGINES

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Publication number
DE2327546A1
DE2327546A1 DE2327546A DE2327546A DE2327546A1 DE 2327546 A1 DE2327546 A1 DE 2327546A1 DE 2327546 A DE2327546 A DE 2327546A DE 2327546 A DE2327546 A DE 2327546A DE 2327546 A1 DE2327546 A1 DE 2327546A1
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Germany
Prior art keywords
lubricant
basic
fuel
proportion
engine
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
DE2327546A
Other languages
German (de)
Inventor
Pierre Bedague
Pierre Marchand
Guy Parc
Fernand Roux
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
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IFP Energies Nouvelles IFPEN
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Application filed by IFP Energies Nouvelles IFPEN filed Critical IFP Energies Nouvelles IFPEN
Publication of DE2327546A1 publication Critical patent/DE2327546A1/en
Pending legal-status Critical Current

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    • 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
    • C10L1/192Macromolecular 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
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • C10M107/34Polyoxyalkylenes
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    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
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    • 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
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    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
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    • 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
    • C10L1/1986Macromolecular 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 complex polyesters
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/25Internal-combustion engines
    • C10N2040/255Gasoline engines
    • C10N2040/26Two-strokes or two-cycle engines

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
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  • Organic Chemistry (AREA)
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  • Lubricants (AREA)

Description

Zusatz zu Patent. Addendum to patent.

Patentanmeldung P 22 63 243.5Patent application P 22 63 243.5

Die -vorliegende Erfindung "betrifft die Schmierung von Zweitakt- und Drehkolbenmotoren.The present invention relates to the lubrication of two-stroke and rotary piston engines.

In dem am 23.Dezember 1972 unter der Nummer ρ 2263243.5 angemeldeten Hauptpatent wird ein Verfahren zum Schmieren von Zweitakt- und Drehkolbenmotoren beschrieben, in welchem dem Motor, der im übrigen auf übliche Weise mit einem Kraftstoff betrieben wird, eine Schmiermittelkomposition zugeführt wird, die aus einem Grundschmiermittel und üblichen Zusätzen besteht und eine Viskosität von mindestens 6 cSt bei 98,90C aufweist, wobei das Grundschmiermittel 20 bis 100 Gew.$ und in manchen Eällen 10 bis 100 Gew.# mindestens eines Polyalkylenglykolderivats enthält, welches ein Äther, ein einfacher Ester, ein komplexer Ester, ein Polyester oder ein Ester von Ithern von Polyalkylenglykolen ist, die der allgemeinen Formel Ϊ0 ( ß - O ^n H entsprechen, in welcher jeder Rest R ein zweiwertiger aliphatischer Rest mit 2 bis 5 Kohlenstoffatomen ist und die Zahl η einen Wert von 2 bis 50 hat.In the main patent applied for on December 23, 1972 under the number ρ 2263243.5, a method for lubricating two-stroke and rotary piston engines is described in which the engine, which is otherwise operated in the usual way with fuel, is supplied with a lubricant composition that is derived from a lubricant base and conventional additives and having a viscosity of at least 6 cSt at 98.9 0 C, wherein the base lubricant 20 to 100 wt. $, and in some Eällen 10 to 100 wt. # of at least one polyalkylene glycol derivative which is an ether, a simple ester, a complex ester, a polyester or an ester of ethers of polyalkylene glycols which correspond to the general formula Ϊ0 (ß - O ^ n H, in which each radical R is a divalent aliphatic radical with 2 to 5 carbon atoms and the number η has a value from 2 to 50.

30 98 50/097 230 98 50/097 2

• -2-• -2-

Das Grundschmiermittel konnte auch andere Bestandteile enthalten, insbesondere übliche Schmiermittel, vor allem Schmieröle mineralischen Ursprungs oder synthetische Schmieröle, Verdünnungsmittel, aromatische lösungsmittel, sauerstoffhaltige Lösungsmittel oder bestimmte Ester.The basic lubricant could also contain other components, especially common lubricants, especially lubricating oils of mineral origin or synthetic lubricating oils, thinners, aromatic solvents, oxygenated solvents or certain esters.

Dadurch, daß das Grundschmiermittel einen beträchtlichen Anteil eines oder mehrere Polyalkylenglykolderivate enthielt, konnte das Schmiermittel in einer im Verhältnis zu der für den Betrieb des Motors erforderlichen Kraftstoffmenge verringerten Menge verwendet werden, die im allgemeinen einer Grundschmiermittelmenge von 0,1 bis 2 Gew.$ bei den Zweitaktmotoren und 50 ppm bis 2 Gew.$ bei den Drehkolbenmotoren entsprach.Because the base lubricant contained a significant proportion of one or more polyalkylene glycol derivatives, was able to reduce the lubricant in an amount relative to the amount of fuel required to run the engine Amount used, generally a base lubricant amount of 0.1 to 2 wt. $ For the two-stroke engines and 50 ppm to 2% by weight for the rotary piston engines corresponded.

Man hat jetzt festgestellt, daß man dadurch, daß man den Grundschmiermitteln bestimmte, nachstehend definierte organische Verbindungen zusetzt, die Eigenschaften der genannten Schmiermittel, vor allem ihre Wirkung gegen das Verklemmen und Festfressen des Kolbens, erheblich verbessern und die Verschmutzung des Motors vermindern kann.It has now been found that by using the basic lubricants adds certain organic compounds defined below, the properties of the lubricants mentioned, especially their effect against jamming and seizing of the piston, significantly improve and the pollution of the engine can decrease.

Diese organischen Verbindungen sind im allgemeinen Monocarbonsäuren mit einer aliphatischen Kette mit 10 bis 18 Kohlenstoffatomen, einfache niedere Alkylester dieser Säuren (der Begriff niedere Alkyle umfasst solche mit 1-8 Kohlenstoffatomen), primäre Monoalkohole und primäre Monoamine, die eine aliphatisch« Kette mit 10 bis 18 Kohlenstoffatomen enthalten, Dicarbonsäuren, die eine aliphatische Kette mit 36 Kohlenstoffatomen besitzen, Tricarbonsäuren, die eine aliphatische Kette mit 54 Kohlenstoffatomen aufweisen und einfache niedere Alkylester dieser Säuren,These organic compounds are generally monocarboxylic acids with an aliphatic chain of 10 to 18 carbon atoms, simple lower alkyl esters of these acids (the term lower alkyl includes those with 1-8 carbon atoms), primary monoalcohols and primary monoamines, which have an aliphatic « Chain with 10 to 18 carbon atoms contain dicarboxylic acids, which are an aliphatic chain with 36 carbon atoms have tricarboxylic acids, which have an aliphatic chain with 54 carbon atoms, and simple lower alkyl esters these acids,

Perner sind hier zu nennen:Perner should be mentioned here:

Monocarbonsäuren mit 10 bis 18 Kohlenstoffatomen mit gesättigter aliphatischer Kette oder ungesättigter Kette wie die Decansauref Dodecansäure, Tetradecansäure, Hexadecänsäure, OctadecansäureMonocarboxylic acids with 10 to 18 carbon atoms with a saturated aliphatic chain or unsaturated chain such as decanoic acid f dodecanoic acid, tetradecanoic acid, hexadecanoic acid, octadecanoic acid

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und Octadecensäure (Ölsäure) und auch die natürlichen Fraktionen, die aus Gemischen von mehreren dieser Säuren bestehen?and octadecenoic acid (oleic acid) and also the natural fractions, which consist of mixtures of several of these acids?

die niederen Allylester dieser Säuren oder Gemische dieser Säuren wie die Methylester, A'thylester, Propylester, Isopropylester» But^ylester, Isobuti^ylester, Pentylester, Hexylester, Heptylester, oder die Äthyl-2-Hexyl-Esterj ·the lower allyl esters of these acids or mixtures of these Acids such as methyl esters, ethyl esters, propyl esters, isopropyl esters » But ^ yl ester, isobuti ^ yl ester, pentyl ester, hexyl ester, Heptyl ester, or the ethyl 2-hexyl esterj

die aliphatischen Monoalkohole mit 10 bis 18 Kohlenstoffatomen wie Decanol, Dodecanol oder Tridecanol, ferner die linear gebauten alkoholischen Fraktionen mit' 10 bis 18 Kohlenstoffät„omen, die man durch. Reduktion der entsprechenden Gemische der Monocarbonsäuren oder durch Synthesen enthält* wie beispielsweise durch Polymerisation von Ithylen in Anwesenheit eines Alkylaluminium-Katalysators mit anschließender Oxydation;the aliphatic monoalcohols with 10 to 18 carbon atoms such as decanol, dodecanol or tridecanol, and also the linear alcoholic fractions with 10 to 18 carbon atoms, which one through. Reduction of the corresponding mixtures of the monocarboxylic acids or by syntheses * such as, for example, by polymerizing ethylene in the presence of an alkylaluminum catalyst with subsequent oxidation;

die primären aliphatischen Monoamine mit 10 bis 18 Kohlenstoffatomen wie Decylamin und Dodecylamin; • die Dicarbonsäuren oder Tricarbonsäuren mit aliphatischen Ketten mit 36 bzw. 54 G-Atomen, die gesättigt oder auch nichtgesättigt sein können und die man durch Dimerisation bzw» Trimerisation von Monocarbonsäuren mit aliphatisch ungesättigter Säure mit 18 G-Atomen enthält, wie der Octadecensäure (Ölsäure) und ihrer Gemische mit Octadecadiensaure (Linol—-säure) und/ oder Octadecatriensäure ( Linolensäure ) » wobei diese Dimerisation (bzw. Irimerisation) gegebenenfalls von einer Hydrierung gefolgt ist.the primary aliphatic monoamines with 10 to 18 carbon atoms such as decylamine and dodecylamine ; • the dicarboxylic acids or tricarboxylic acids with aliphatic chains with 36 or 54 G atoms, which can be saturated or unsaturated and which are obtained by dimerization or »trimerization of monocarboxylic acids with aliphatically unsaturated acid with 18 G atoms, such as octadecenoic acid (oleic acid ) and their mixtures with octadecadienoic acid (linoleic acid) and / or octadecatrienoic acid (linolenic acid) »where this dimerization (or irimerization) is optionally followed by a hydrogenation.

Die oben beschriebenen organischen Verbindungen werden gemäß vorliegender Erfindung in einem Mengenverhältnis von 0,1 bis 40 Gew.^ und vorzugsweise von 5 bis 25 Gew.# bezogen auf das Basisschmiermittel eingesetzt.The organic compounds described above are according to The present invention in an amount ratio of 0.1 to 40 wt. ^ and preferably from 5 to 25 wt. # Based on the Basic lubricant used.

Bevorzugt werden die Verbindungen, die eine aliphatieehe Kette mit 12 Kohlenstoffatomen aufweisen* Die Do dec ansäur ejund deren Ester niederer Alkyle, das Dodecanol und das Dodecylaain. .Preferred are the compounds which have an aliphatic chain with 12 carbon atoms have * The Do dec ansäur ejund their Lower alkyl esters, dodecanol and dodecylaain. .

Wie in dem Hauptpatent, kann man dem Grundschmiermittel verschiedene übliche Zusätze beigeben, und zwar?As in the main patent, the basic lubricant can be different add the usual additives, namely?

- Antioxydantien, z.B. von der Art des Phenols oder des Amins, z.B. zu einem Anteil von 0,1 bis 10$ im Verhältnis zu.dem Gewicht des Sehmiermittels; ...- Antioxidants, e.g. of the phenol or amine type, e.g. in a proportion of 0.1 to 10 $ in relation to the weight of the seeping agent; ...

.3098 50/0972.3098 50/0972

— oberflächenaktive Zusätze in Form von organischen Salzen und aschefreie Dispergiermittel, z.B. zu einem Anteil von 0,05 bis 30$ und vorzugsweise 5 bis 20$ im "Verhältnis zu dem Gewicht des Schmiermittels.- Surface-active additives in the form of organic salts and ashless dispersants, e.g. Lubricant.

Ferner kann man dem G-rundschmiermittel bestimmte halogenhalt ige Derivate, wie z.B. das Ä'thylendibromid, zusetzen, die die Bleiverbindungen eliminieren sollen, welche in der Verbrennungskammer entstehen können, wenn der verwendete Kraftstoff Blei enthält (Bleitetraäthyl oder Bleitetramethyl).You can also add certain halogen-containing lubricants to the basic lubricant Add derivatives, such as ethylene dibromide, which form the lead compounds to eliminate which can occur in the combustion chamber if the fuel used contains lead (Tetraethyl lead or tetramethyl lead).

Wie in dem Hauptpatent können die so definierten Schmiermittelkompositionen den Zweitaktmotoren zu einem Anteil zugeführt werden, der einer Grundschmiermittelmenge von 0,1 bis 2 Gew.$ im Verhältnis zu der für den Betrieb des genannten Motors erforderlichen Kraftstoffmenge entspricht. Bei den Drehkolbenmotoren kann dieser Anteil einer Grundschmiermittelmenge von 50 ppm bis 2 Gew.$ im Verhältnis zu der Kraftstoffmenge entsprechen.As in the main patent, the lubricant compositions thus defined the two-stroke engines are supplied in a proportion that corresponds to a basic lubricant quantity of 0.1 to 2 wt Corresponds to the ratio to the amount of fuel required to operate the said engine. With the rotary piston engines this proportion can correspond to a basic lubricant quantity of 50 ppm to 2 wt. $ in relation to the fuel quantity.

Im Falle der mit einem fertigen ipräformierten) Kraftstoff-Schmiermittelgemisch betriebenen Zweitaktmotoren bestehen die Kraftstoff-Schmiermittelgemische wie in dem Hauptpatent aus einem üblichen Kraftstoff, dem eine Menge eines Schmiermittelendpraduktes zugesetzt worden ist, die einer Menge eines Grundschmiermittels der vorstehenden Definition von 0,1 bis 2 Gew.^ im Verhältnis zu dem genannten Kraftstoff entspricht. Bei den mit einem fertigen Kraftstoff-Schmiermittelgemisch betriebenen Dreakolbenmotoren entspricht der Anteil an dem Kraftstoff zugesetztem Schmiermittelendprodukt einer Grundschmieniiittelmenge von 50 ppm bis 2 Gew.$> im Verhältnis zu dem genannten Kraftstoff.In the case of the two-stroke engines operated with a finished (preformed) fuel-lubricant mixture, the fuel-lubricant mixtures consist, as in the main patent, of a conventional fuel to which an amount of a final lubricant product has been added that corresponds to an amount of a basic lubricant as defined above from 0.1 to 2 Weight ^ in relation to the fuel mentioned. At the finished with a fuel-lubricant mixture powered Dreakolbenmotoren the proportion of the fuel added lubricant end product corresponds to 2 ppm by weight of a Grundschmieniiittelmenge 50. $> Relative to said fuel.

Die nachstehenden Beispiele dienen der Erläuterung der vorliegenden Erfindung.The following examples serve to illustrate the present Invention.

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Man hat zum einen das Bis-octadecenoat eines Polyäthylenglyköls des Molekulargewichts 600 hergestellt. Die viskosimetrischen Merkmale dieses als Produkt I gekennzeichneten Esters sind die folgenden:One has the bis-octadecenoate of a polyethylene glycol of molecular weight 600 produced. The viscometric characteristics of this ester identified as Product I are the following:

Viskosität bei 98,9°C..... 12,7 cStViscosity at 98.9 ° C ..... 12.7 cSt

Viskosität bei 37,8°C..... 66,9 cStViscosity at 37.8 ° C ..... 66.9 cSt

Viskositätsindex (VI1,).......... 205 ■Viscosity index (VI 1 ,) .......... 205 ■

Man hat zum anderen das Bis-heptanoat eines Polypropylenglykols des Molekulargewichts 2000 hergestellt. Die viskosimetrischen Merkmale dieses als Produkt II gekennzeichneten Esters sind die folgenden:On the other hand, there is the bis-heptanoate of a polypropylene glycol of molecular weight 2000. The viscometric characteristics of this ester labeled as Product II are the following:

Viskosität bei 98,9°C... 19,1 cStViscosity at 98.9 ° C ... 19.1 cSt

Viskosität bei 37,80C... .118,0 cStViscosity at 37.8 0 C ... .118,0 cSt

Viskositätsindex (VLg) .192Viscosity index (VLg) .192

Man hat die Klemmeigenschaften der Grundschmiermittel, deren Zusammensetzung in der nachstehenden Tabelle angegeben ist I, getestet.One has the clamping properties of the basic lubricants, the composition of which is given in the table below I, tested.

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Tabelle ITable I.

i Grund-
{ schmier-
j mittel
i basic
{lubricating
j medium
-- Zusammensetzungcomposition Menge
(Gew. $6)
lot
(Wt. $ 6)
Zusatzadditive Menge
j(Gew.$)
lot
j (wt. $)
Poly alkyl englykolderivatPoly alkyl englycol derivative 100100 ArtArt ! A! A. ArtArt 9595 5 -I5 -I Produkt IProduct I. 9595 LaurinsäureLauric acid 5 j
-
5 y
-
; c
; c
100100 IsopropyldodecanoatIsopropyl dodecanoate ■Μ■ Μ
DD. »» 9595 55 EE. Produkt IIProduct II 9595 LaurinsäureLauric acid 55 ;; ΈΈ trtr 9595 MethyldodecanoatMethyl dodecanoate 55 GG IlIl ■ 95■ 95 DodecanolDodecanol 5 I5 I. HH MM. DodecylaminDodecylamine ItIt

Diese Grundschmiermittel wurden zwecks Ermittlung ihrer Klenonfestigkeitseigenschaften in einem Zweitaktmotor Marke Motobecane, Typ AY?L, in "Kraftstoff-Schmiermittel"-Gemischen, und 25war 1 Gew.^ Schmiermittel in einem gewöhnlichen bleifreien Benzin mit der Resaarchoktanzahl 94, getestet.These base lubricants were used to determine their clenon resistance properties in a two-stroke engine brand Motobecane, type AY? L, in "fuel-lubricant" mixtures, and 25 was 1% by weight of lubricant in an ordinary unleaded gasoline with a resaarchoct number of 94, tested.

Um die Klemmfestigkeitseigenschaften der getesteten Gemische zu ermitteln, hat man den Temperaturanstieg des Zündkerzenknie-Stücks gemessen, der durch einen Geschwindigkeitsabfall des Motors um 400 Umdrehungen pro Miruite infolge einer Verklemmung desTo determine the clamp strength properties of the mixtures tested, one has the temperature rise of the spark plug knee piece measured by a speed drop of the motor of 400 revolutions per Miruite due to a jamming of the

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Kolbens. in dem Zylinder verursacht worden ist, zu der es kommt, wenn die Kühlung des Motors unterbrochen wird. Ein Schmiermittel ist umso besser, je größer der Temperaturanstieg ist, den das jeweilige Schmiermittel zuläßt. .Piston. has been caused in the cylinder that occurs if the cooling of the motor is interrupted. The greater the temperature rise, the better a lubricant is Lubricant. .

Die in der nachfolgenden Tabelle II aufgeführten Ergebnisse sind in Prozent der Verbesserung im Verhältnis, zu dem Bezugsprodukt (Produkt I allein für. die Schmiermittel B und C und Produkt II allein für die Schmiermittel. E bis. H) ausgedrückt und wie folgt erhalten worden: - - . "<The results listed in Table II below are a percentage of the improvement in relation to the reference product (Product I only for lubricants B and C and product II solely for the lubricants. E to. H) and obtained as follows: - -. "<

Verbesserung (#) =Improvement (#) =

χ 100χ 100

ABqABq

wobei Δ θ-j und Δ Bq den Temperaturanstieg darstellen, der für das getestete Gemisch bzw. für das Bezugsprodukt gemessen wurde.where Δ θ-j and Δ Bq represent the temperature rise necessary for the mixture tested or for the reference product was measured.

TabelleTabel

IIII

Getestetes -SchmiermittelTested lubricant

A (Bezugsprodukt)A (reference product)

D (Bezugsprodukt) E .J1 G HD (reference product) E .J 1 GH

Anteil in dem Benzin (Gew.$)Share in the gasoline (wt. $)

Verbesserungimprovement

11 99 11 77th 11 OO 11 77th 11 99 11 33 r ,.r,. 88th

Diese Ergebnisse zeigen die Bedeutung des Zusatzes von organischen C^ ,,-Verbindungen zu dem GrundschmiermittelThese results show the importance of adding organic ingredients C ^ ,, - compounds to the base lubricant

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Man hat aie nachstehenden Schmiermittelkompositionen hergestellt;The following lubricant compositions have been prepared;

- Bis-dodecanoat eines Polypropylenglykols des Molekulargewichts 1200 76- Bis-dodecanoate of a polypropylene glycol with a molecular weight of 1200 76

- Oberflächenaktives Mittel und aschefreies Dispergiermittel 16- Surfactant and ashless dispersant 16

- ρ,ρ-Dioctyldiphenylamin 6- ρ, ρ-dioctyldiphenylamine 6

- Phenyl-ß-naphthylamin 2- Phenyl-ß-naphthylamine 2

Komposition EComposition E

Man hat die Herstellung der Komposition J wiederholt, hat jedoch einen Teil des Bis-dodecanoat des Polypropylenglykols durch Methyldodecanoat ersetzt, und zwar 1-0$ des Gewichts der gesamten Komposition.The preparation of composition J was repeated, but some of the bis-dodecanoate of polypropylene glycol was replaced by methyl dodecanoate replaced, namely 1-0 $ the weight of the entire composition.

Die getesteten "Kraftstoff-Schmiermittelll-Gemische enthalten jeweils. 0,5 Gew.# der Kompositionen J und K in einem gewöhnlichen bleifreien Benzin mit der Researchoktanzahl um 94.The "fuel-lubricant II mixtures" tested each contain 0.5% by weight of the compositions J and K in an ordinary unleaded gasoline with a research octane number of around 94.

Der nach der Methode CEC \ 402 T 68 an einem Zweitaktmotor der Marke Motobecane, Typ AV 7 I>, durchgeführte Verschmutzungstest dauert 100 Stunden,The contamination test carried out according to the method CEC \ 402 T 68 on a two-stroke engine of the Motobecane brand, type AV 7 I>, takes 100 hours,

Er besteht aus verschiedenen Betriebsphasen, u.a. einer Phase mit gedrosseltem Motor. Er ist repräsentativ für einen tatsächlichen Betrieb von längerer Dauer.It consists of different operating phases, including one phase with throttled engine. It is representative of an actual one Long-term operation.

Man hat die Motorverschmutzung in % ermittelt und die verbesserte Wirkung bei Kolben und Zylinder unter Zugrundlegung der Bezugszahl 100 gemessen.The engine contamination was determined in% and the improved effect on the piston and cylinder was measured using the reference number 100 as a basis.

Die Ergebnisse sind in der nachstehenden Tabelle III angegeben.The results are given in Table III below.

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- -

Tabelle IIITable III

■■■■ Yers chmutzungYers pollution Messung/100
Kolben-Zylinder
Measurement / 100
Piston Cylinder
I Komposition J
Komposition K
I composition J
Composition K
44,2
18,0
44.2
18.0
61,9
94,7
61.9
94.7

Diese Ergebnisse zeigen, wie sehr der erfindungsgemäße Zusatz einer organischen C1^-Verbindung zu dem G-rundschmiermittel der Motorverschmutzung entgegenwirkt.These results show how much the inventive addition of an organic C 1 ^ compound to the basic lubricant counteracts engine pollution.

309850/0972309850/0972

Claims (9)

1) Verfahren zum Schmieren eines Zweitakt- oder Drehkolbenmotors mittels einer Schmiermittelkomposition, die eine Viskosität von mindestens 6 cSt "bei 98,90C aufweist und aus üblichen Zusätzen und einem Grundschmiermittel besteht, das 10 bis 100 Gew.?6 mindestens eines Polyalkylenglykolderivats gemäß dem Hauptpatent enthält, dadurch gekennzeichnet, daß ein Anteil von 0,1 bis 40 Gew.$ des genannten Grundschmiermittels durch den äquivalenten Anteil mindestens einer organischen Verbindung ersetzt wird, und zwar durch eine der Monocarbonsäuren mit einer aliphatischen Kette mit 10 bis 18 Kohlenstoffatomen, einen ihrer einfachen Ester niederer Alkyle, einen Monoalkohol oder ein primäres Monoamin mit einer aliphatischen Kette mit 10 bis 18 Kohlenstoffatomen, eine Dicarbonsäure mit einer aliphatischen Kette mit 36 Kohlenstoffatomen, eine der Tricarbonsäuren mit einer aliphatischen Kette mit 54 Kohlenstoffatomen oder einen einfachen Ester niederer Alkyle dieser Säuren.1) Method for lubricating a two-stroke or rotary piston engine by means of a lubricant composition which has a viscosity of at least 6 cSt "at 98.9 0 C and consists of conventional additives and a basic lubricant that contains 10 to 100 wt.? 6 of at least one polyalkylene glycol derivative contains the main patent, characterized in that a proportion of 0.1 to 40 wt. $ of said base lubricant is replaced by the equivalent proportion of at least one organic compound, namely by one of the monocarboxylic acids with an aliphatic chain with 10 to 18 carbon atoms, a their simple esters of lower alkyls, a monoalcohol or a primary monoamine with an aliphatic chain with 10 to 18 carbon atoms, a dicarboxylic acid with an aliphatic chain with 36 carbon atoms, one of the tricarboxylic acids with an aliphatic chain with 54 carbon atoms or a simple ester of lower alkyls of these acids . 2) Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die genannte organische Verbindung 5 bis 25 Gew.% des Grundschmiermittels darstellt.2) Method according to claim 1, characterized in that the said organic compound 5 to 25% by weight of the base lubricant represents. 3) Verfahren nach einem der Ansprüche 1 und 2, dadurch gekennzeichnet, daß die genannte organische Verbindung die Laurinsäure, einer ihrer einfachen Ester niederer Alkyle, das Dodecanol oder das Dodecylamin ist.3) Method according to one of claims 1 and 2, characterized in that that said organic compound is lauric acid, one of their simple esters of lower alkyls, which is dodecanol or dodecylamine. 4) Verfahren nach Anspruch 1, wobei das Grundschmiermittel im wesentlichen aus mindestens einem Polyalkylenglykolderivat besteht, dadurch gekennzeichnet, daß ein Anteil von 0,1 bi3 40 Gew.# des genannten Grundschmiermittels durch den äquivalenten Anteil mindestens einer organischen Verbindung gemäß der Definition von Anspruch 1 ersetzt ist.4) The method of claim 1, wherein the base lubricant im consists essentially of at least one polyalkylene glycol derivative, characterized in that a proportion of 0.1 to 3 40 wt. # Of the base lubricant mentioned by the equivalent proportion of at least one organic compound according to the definition of claim 1 is replaced. 3 09850/09723 09850/0972 5) Verfahren nach. Anspruch 4, dadurch gekennzeichnet, daß die genannte organische Verbindung 5 bis 25 Gew.$ des Grundsehmiermittels darstellt.5) procedure according to. Claim 4, characterized in that said organic compound 5 to 25% by weight of the basic seizing agent represents. 6) Verfahren nach einem der Ansprüche 1 bis 5 zum Sehmieren eines Zweitaktmotors, wobei die Sphmiermittelkomposition dem Motor zu einem Anteil, der einer Grundschmiermittelmenge von 0,1 bis 2 Gew.% im Verhältnis zu der für den Betrieb des genannten Motors erforderlichen Kraftstoffmenge entspricht, zugeführt wird. .,·.-.6) The method according to any one of claims 1 to 5 for Sehming a Two-stroke engine, the Sphmiermittelkomposition the engine to a proportion that a basic amount of lubricant of 0.1 Up to 2% by weight in relation to the amount of fuel required for the operation of said engine, is supplied will. ., · .-. 7) Verfahren nach einem der Ansprüche 1 bis 5 zum Schmieren eines Drehkolbenmotors, wobei die Schmiermittelkomposition dem Motor zu einem Anteil, der einer Grundschmiermittelmenge von 50 ppm bis 2 Gew.% im Verhältnis zu der für den Betrieb des genannten Motors erforderlichen Kraftstoff menge entspricht, zugeführt wird.7) Method according to one of claims 1 to 5 for lubricating a Rotary piston engine, the lubricant composition of the engine to a proportion that corresponds to a basic amount of lubricant 50 ppm to 2% by weight in relation to the amount of fuel required to operate the specified engine, is fed. 8) Kraftstoff-Schmiermittelgemisch für den Betrieb eines Zweitaktmotors, das aus einem üblichen Kraftstoff und einer Schmiermitt elkompo sit ion, die sich aus einem Grundschmiermittel und üblichen Zusätzen zusammensetzt und eine Viskosität von mindestens 6 cSt bei 98,90C aufweist, besteht und in dem der Anteil an Schmiermittelkomposition einer Grundschmiermittelmenge von 0,1 bis 2 Gew.% im Verhältnis zu dem genannten Kraftstoff entspricht, dadurch gekennzeichnet, daß das genannte Grundschmiermittel wie in einem der Ansprüche 1 bis 5 definiert ist.8) Fuel-lubricant mixture for the operation of a two-stroke engine, which consists of a common fuel and a lubricant elkompo sit ion, which is composed of a basic lubricant and common additives and has a viscosity of at least 6 cSt at 98.9 0 C, and in which the proportion of lubricant composition corresponds to a basic lubricant amount of 0.1 to 2% by weight in relation to the said fuel, characterized in that the said basic lubricant is as defined in one of claims 1 to 5. 9) Kraftstoff-Schmiermittelgemisch für den Betrieb eines Ilrehkolbenmotors, das aus einem üblichen Kraftstoff und einer Schmiermittelkomposition, die sich aus einem Grundschmiermittel und üblichen Zusätzen zusammensetzt und eine Viskosität von mindestens 6 cSt bei 98,90C aufweist, besteht und in dem der Anteil an Schmiermittelkomposition einer Grundschmiermittelmenge von 50 ppm bis 2 Gew.% im Verhältnis zu dem.genannten Kraftstoff entspricht, dadurch gekennzeichnet, daß das genannte Grundschmiermittel wie in einem der -Ansprüche 1 bis 5 definiert ist. * yr 9) Fuel-lubricant mixture for the operation of a rotary piston engine, which consists of a common fuel and a lubricant composition, which is composed of a basic lubricant and common additives and has a viscosity of at least 6 cSt at 98.9 0 C, and in which the proportion of lubricant composition corresponds to a basic lubricant amount of 50 ppm to 2% by weight in relation to the fuel mentioned, characterized in that the said basic lubricant is defined as in one of claims 1 to 5. * yr 309850/0972309850/0972
DE2327546A 1971-12-31 1973-05-30 METHOD OF LUBRICATING TWO-STROKE AND ROTARY LISTON ENGINES Pending DE2327546A1 (en)

Applications Claiming Priority (4)

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FR7147887A FR2169718B1 (en) 1971-12-31 1971-12-31
FR7220040A FR2187893B2 (en) 1971-12-31 1972-06-02
US31987172A 1972-12-29 1972-12-29
US366014A US3871837A (en) 1971-12-31 1973-06-01 Method for lubricating 2-stroke engines and rotary engines

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BE (1) BE799904R (en)
CA (1) CA996538A (en)
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FR (2) FR2169718B1 (en)
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CA996538A (en) 1976-09-07
FR2187893B2 (en) 1974-10-25
GB1425661A (en) 1976-02-18
US3871837A (en) 1975-03-18
FR2187893A2 (en) 1974-01-18
FR2169718B1 (en) 1974-09-13
BE799904R (en) 1973-11-23
GB1417590A (en) 1975-12-10
NL7307707A (en) 1973-12-04
DE2263243A1 (en) 1973-07-12
FR2169718A1 (en) 1973-09-14
NL7300029A (en) 1973-07-03

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