DE1018572B - lubricant - Google Patents
lubricantInfo
- Publication number
- DE1018572B DE1018572B DEW10942A DEW0010942A DE1018572B DE 1018572 B DE1018572 B DE 1018572B DE W10942 A DEW10942 A DE W10942A DE W0010942 A DEW0010942 A DE W0010942A DE 1018572 B DE1018572 B DE 1018572B
- Authority
- DE
- Germany
- Prior art keywords
- lubricant
- tin
- naphthylamine
- oil
- aromatic
- 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
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/402—Castor oils
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
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- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
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- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/066—Arylene diamines
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/14—Containing carbon-to-nitrogen double bounds, e.g. guanidines, hydrazones, semicarbazones
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- C10M2215/22—Heterocyclic nitrogen compounds
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- C10M2215/221—Six-membered rings containing nitrogen and carbon only
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- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
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- C10M2215/226—Morpholines
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- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- C10M2219/046—Overbasedsulfonic acid salts
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- 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)
- Lubricants (AREA)
Description
DEUTSCHESGERMAN
Die Erfindung bezieht sich auf die Zusammensetzung von Schmiermitteln, insbesondere auf solche für Verbrennungsmotoren .The invention relates to the composition of lubricants, particularly those for internal combustion engines .
Bekanntlich besitzt Rizinusöl gewisse Eigenschaften, welche dasselbe zu einem hervorragenden Schmiermittel machen. So z. B. verschafft ihm die Fähigkeit, verhältnismäßig hohe Belastungen bzw. Flächendrücke ohne Abreißen des Ölfilms auszuhalten, zusammen mit seinem sehr niedrigen Reibungskoeffizienten unter den Verhältnissen der Grenzschmierung einen einzigartigen Platz unter den Schmiermitteln.As is well known, castor oil has certain properties which make it an excellent lubricant do. So z. B. gives him the ability to handle relatively high loads or surface pressures without Withstands tearing of the oil film, together with its very low coefficient of friction under the conditions boundary lubrication has a unique place among lubricants.
Rizinusöl und Gemische von Rizinusöl mit Mineralschmierölen sind in ausgedehntem Maße für die Schmierung von Verbrennungsmotoren, insbesondere von solchen, die unter hoher Belastung und bei hoher Drehzahl zu arbeiten haben, verwendet worden.Castor oil and mixtures of castor oil with mineral lubricating oils are extensively used for lubrication of internal combustion engines, especially those that are under high load and at high speed have been used to work.
Bisher litten aber derartige Schmiermittel unter dem Nachteil, daß sie nur innerhalb eines sehr beschränkten Viskositätsbereiches verfügbar waren. Mineralische Schmieröle sind dagegen bekanntlich in einem sehr großen Viskositätsbereich verfügbar, und derartige Öle sind zum Schmieren von Verbrennungsmotoren mit Viskositäten von etwa 50 bis 400 Redwood-Sekunden bei 60° C, d. h. in einem Bereich von 5 W — 50 gemäß der Klassifikation der Society of Automotive Engineers (SAE) verwendet worden.So far, however, such lubricants have suffered from the disadvantage that they can only be used within a very limited range Viscosity range were available. Mineral lubricating oils, on the other hand, are known to be very much wide viscosity range available, and such oils are used for lubricating internal combustion engines with Viscosities of about 50 to 400 Redwood seconds at 60 ° C; i.e. H. in a range of 5 W - 50 according to the classification of the Society of Automotive Engineers (SAE) has been used.
Gemäß einem älteren Erfindungsvorschlag wurden auch schon Schmiermittel auf der Basis von Rizinusöl mit einem darin leichtlöslichen Mono- oder Diester sowie mit aromatischen, primären, sekundären und tertiären Aminen versetzt. Nach einem weiteren älteren Vorschlag können Schmiermittel auf der Basis von Rizinusöl geringe Mengen organischer Zinn- oder Antimonverbindungen und aromatische oder heterocyclische sekundäre Mono- oder Polyamine enthalten.According to an older proposal of the invention, lubricants based on castor oil with a Easily soluble mono- or diesters therein and mixed with aromatic, primary, secondary and tertiary amines. According to another older suggestion, castor oil-based lubricants can be used in small quantities organic tin or antimony compounds and aromatic or heterocyclic secondary mono- or polyamines contain.
Die Viskosität von Rizinusöl wurde bislang bis zu einem gewissen Maße dadurch geändert, daß man es mit Mineralölen verschiedener Viskositäten mischte, aber durch diese Hilfsmittel konnte man nur geringere Änderungen der Viskosität herbeiführen, und zwar wegen der beschränkten Löslichkeit des Mineralöls in Rizinusöl (höchstens etwa 15 Gewichtsprozent).The viscosity of castor oil has heretofore been altered to some extent by treating it with mineral oils different viscosities mixed, but only minor changes in the Induce viscosity because of the limited solubility of mineral oil in castor oil (at most about 15 percent by weight).
Ein anderer Nachteil, der mit der Verwendung von Schmiermitteln, die ganz oder in der Hauptsache aus Rizinusöl bestehen, verbunden ist, ist deren Neigung gewesen, im Motor und auf äußeren Teilen, wie z. B. auf den Auspuffrohren, usw. zu verharzen, was einen häufigen Ölwechsel und die Reinigung der verharzten Teile erforderlich macht. Verbesserte Schmiermittel, mit wesentlich herabgesetzter Neigung zur Verharzung, sind Gegenstand des Patents 909 243.Another drawback that comes with the use of lubricants, in whole or in the main Castor oil is related, its tendency has been in the engine and on external parts, such as. B. on resinification of the exhaust pipes, etc., which requires frequent oil changes and cleaning of the resinous parts power. Improved lubricants, with a significantly reduced tendency to resinify, are the subject of patent 909 243.
Es ist klar, daß die Viskosität eines Öles, welches zum Schmieren eines Verbrennungsmotors verwendet werden soll, von der Konstruktion des Motors abhängen wird.It is clear that the viscosity of an oil which can be used for lubricating an internal combustion engine will depend on the design of the engine.
Schmiermittellubricant
Anmelder:Applicant:
C. C. Wakefield & Company Limited,
LondonCC Wakefield & Company Limited,
London
Vertreter: Dr. M. Eule, Patentanwalt,
München 13, Kurfürstenplatz 2Representative: Dr. M. Eule, patent attorney,
Munich 13, Kurfürstenplatz 2
Beanspruchte Priorität:
Großbritannien vom 28. Januar 1S53Claimed priority:
Great Britain January 28, 1S53
So z. B. ergeben gewisse Motoren, die so konstruiert sind, daß sie mit Schmierölen verhältnismäßig niedriger Viskosität, beispielsweise SAE10 W oder 20, in Betrieb gehalten werden können, keinen so wirksamen Betrieb mit Ölen von der Viskosität des SAE 40/50-Bereiches und können daher auch nicht so wirkungsvoll mit Rizinusöl oder mit den üblichen Gemischen von Rizinusöl und Mineralöl, wie sie bisher verwendet worden sind, geschmiert werden. Andererseits können einige dieser Motoren, z. B. die Motoren gewisser Rennwagen, infolge der bei denselben auftretenden hohen Kolbengeschwindigkeiten nicht so zufriedenstellend mit Mineralölen geschmiert werden.So z. B. result in certain engines that are designed to operate with relatively low viscosity lubricating oils, for example SAE10 W or 20, kept in operation cannot and cannot operate as effectively with oils of the viscosity of the SAE 40/50 range therefore not as effective with castor oil or with the usual mixtures of castor oil and mineral oil, as they have been used up to now, are lubricated. On the other hand, some of these motors, e.g. B. the engines certain racing cars, not as satisfactory due to the high piston speeds that occur at the same be lubricated with mineral oils.
Es ist demzufolge ein Ziel der vorliegenden Erfindung, ein Schmiermittel zu schaffen, insbesondere ein solches für Verbrennungsmotoren, welches einen beträchtlichen Anteil an Rizinusöl enthält, dessen Viskosität aber erheblich niedriger ist als die des Rizinusöls.It is accordingly an object of the present invention to provide a lubricant, in particular such for internal combustion engines, which contains a considerable proportion of castor oil, but its viscosity is considerable is lower than that of castor oil.
Ein weiteres Ziel der vorliegenden Erfindung geht dahin, ein Schmiermittel zu schaffen, welches Rizinusöl enthält, aber eine verminderte Neigung zur Verharzung besitzt. Das erfindungsgemäße Schmiermittel besteht demzufolge aus einem Gemisch von Rizinusöl, mindestens einem Ester der allgemeinen FormAnother object of the present invention is to provide a lubricant containing castor oil, but has a reduced tendency to resinify. The lubricant according to the invention therefore exists from a mixture of castor oil, at least one ester of the general form
(CH2 (CH 2
COOR1 COOR 1
COOR,COOR,
wobei η eine Zahl von 2 bis 8 einschließlich bedeutet und R1 und R2 identisch und verzweigtkettige Alkylreste oder alkylsubstituierte Cycloalkylreste mit mindestens 5 Kohlenstoffatomen sind, einer geringen Menge, mindestenswhere η is a number from 2 to 8 inclusive and R 1 and R 2 are identical and branched-chain alkyl radicals or alkyl-substituted cycloalkyl radicals having at least 5 carbon atoms, a small amount, at least
70S· "36/33670S · "36/336
eines aromatischen oder heterocyclischen, sekundären Mono- oder Polyamins, welches mindestens drei cyclische Kerne, von denen mindestens zwei aromatischer Natur und direkt mit dem Stickstoffatom verbunden sind, besitzt, sowie einer organischen Verbindung des Zinns und/ oder Antimons und gegebenenfalls einem Zusatz von Mineralöl.an aromatic or heterocyclic, secondary mono- or polyamine, which has at least three cyclic Has nuclei, of which at least two are aromatic in nature and are directly connected to the nitrogen atom, and an organic compound of tin and / or antimony and optionally an addition of Mineral oil.
Die zu verwendenden Ester sollten verhältnismäßig nichtflüssig sein, d. h., sie sollten einen Siedepunkt von mindestens 2000C haben, und sie sollten sich bei den normalen Betriebstemperaturen leicht mit Rizinusöl mischen lassen.The esters to be used should be relatively non-liquid, ie they should have a boiling point of at least 200 ° C. and they should be easy to mix with castor oil at normal operating temperatures.
Beispiele für spezifische Ester, welche gemäß der vorliegenden Erfindung verwendet werden können, sind:Examples of specific esters which can be used in accordance with the present invention are:
Diester der Adipin- und Sebacinsäure mit einem Gemisch von verzweigtkettigen C7—Cg-Alkoholen, Di-(2-Äthyl-hexyl)-azelat, Di-(2-äthyl-hexyl)-sebacat, Di-(3:3:5-trimethyl - hexyl) - sebacat, Di - capryl - sebacat, Sebacinsäurediester mit einem Gemisch von verzweigtkettigen C7—Cg-Alkoholen.Diesters of adipic and sebacic acid with a mixture of branched-chain C 7 -Cg alcohols, di- (2-ethylhexyl) azelate, di- (2-ethylhexyl) sebacate, di- (3: 3: 5 -trimethyl-hexyl) -sebacate, di-capryl-sebacate, sebacic acid diester with a mixture of branched C 7 -Cg alcohols.
Die relativen Anteile des Rizinusöls und des oder der zu verwendenden Ester hängen von der gewünschten Viskosität der endgültigen Mischung ab. Es können alle Gemische in dem Bereich von 10 Gewichtsprozent Rizinusdationsmittel, wie z. B. öllösliche Metallsalze organischer Dithiophosphorsäuren oder Metallderivate alkylierter Phenylthioäther oder Disulfide enthalten.The relative proportions of castor oil and ester (s) to be used will depend on the one desired Viscosity of the final mixture. All mixtures in the range of 10 percent by weight castor additive, such as B. oil-soluble metal salts of organic dithiophosphoric acids or metal derivatives alkylated Contain phenyl thioethers or disulfides.
Spezifische Beispiele für Kombinationen von Zusatzstoffen, welche irgendeinem der vorstehenden Gemische einverleibt werden können, sind:Specific examples of combinations of additives incorporating any of the above mixtures can be incorporated are:
1. 1,0 % Phenyl-jS-naphthylamin, 0,2 % Zinnpetroleumsulf onat ;1. 1.0% phenyl-jS-naphthylamine, 0.2% tin petroleum sulf onat;
2. 0,5 0Z0 Phenyl-ß-naphthylamin, 0,2 °/0 Zinnpetroleumsulfonat, I1O0Z0 Di-(3-carbomethoxy-4-oxyphenyl)-thioäther-kresyl-phosphit, 0,2 0Z0 Di-morpholinyl-phenyl-methan; 2. 0.5 0 0 Z phenyl-.beta.-naphthylamine, 0.2 ° / 0 Zinnpetroleumsulfonat, I 1 O 0 Z 0 di- (3-carbomethoxy-4-oxyphenyl) thioether-cresyl phosphite, 0,2 0 Z 0 di-morpholinyl-phenyl-methane;
3. 0,25 °/0 Zink-di-(a-methyl-isoamyl)-dithiophosphat, 0,10Z0 Calciumpetroleumsulfonat.3. 0.25 ° / 0 Zinc di- (a-methyl-isoamyl) dithiophosphate, 0.1 0 0 Z calcium petroleum sulfonate.
1S Um das Verhalten der erfindungsgemäßen Schmiermittel auszuwerten, wurden die folgenden Motorenteste ausgeführt. 1 S In order to evaluate the behavior of the lubricants according to the invention, the following engine tests were carried out.
A. Lauson-MotorentestA. Lauson engine test
Die Teste wurden mit einem normalen H-2-Lauson-Motor unter den folgenden Verhältnissen vorgenommen:The tests were carried out with a normal H-2 Lauson engine under the following conditions:
Kühlmanteltemperatur:
Ölsumpftemperatur:
Versuchsdauer:
Drehzahl:Cooling jacket temperature:
Oil sump temperature:
Test duration:
Rotational speed:
öl und 90 Gewichtsprozent Ester bis zu 90 Gewichtsprozent Rizinusöl und 10 Gewichtsprozent Ester verwendet werden.oil and 90 percent by weight ester up to 90 percent by weight castor oil and 10 percent by weight ester are used will.
Bei einer Ausführungsform der vorliegenden Erfindung wird auch ein Anteil an Mineralöl in das Gemisch aufgenommen. Sowohl die Menge des verwendeten Mineralöls 30 wendet wurde (Gemisch B). als auch dessen Viskosität hängen von den relativen An- Das Gemisch A bestandIn one embodiment of the present invention, a proportion of mineral oil is also included in the mixture. Both the amount of mineral oil used 30 was applied (mixture B). as well as its viscosity depend on the relative composition
teilen des vorhandenen Rizinusöls und Esters ab und ebenso von der gewünschten Viskosität der endgültigen Mischung. Die Verwendung der erfindungsgemäßen Ester 990C ± I1Il0C 1380C ± I1Il0C 60 Stunden 1840 Umdrehungen/Minutedivide off the castor oil and ester present and also the desired viscosity of the final mixture. The use of the esters according to the invention 99 0 C ± I 1 II 0 C 138 0 C ± I 1 II 0 C 60 hours 1840 revolutions / minute
Die folgenden Versuchsergebnisse veranschaulichen das Verhalten eines typischen Schmiermittelgemisches (Gemisch A) gemäß der vorliegenden Erfindung im Vergleich zu einem Gemisch höherer Viskosität, wie es bisher ver-The following test results illustrate the behavior of a typical lubricant mixture (mixture A) according to the present invention in comparison to a mixture of higher viscosity, as it has been previously
aus 49°/0 Rizinusöl ersterfrom 49 ° / 0 castor oil first
Pressung, 13% Mineralöl B (wie vorher angegeben), 190Z0 Di-(2-äthyl-hexyl)-sebacat, 19% Di-(3 : 3: 5-trimethyl-hexyl)-sebacat zuzüglich 1 %Di-(3-carbomethoxygestattet aber die Einverleibung von praktisch mehr 35 4-oxyphenyl)-thioäther-kresyl-phosphit, 0,5 °/0 Phenyl-Mineralöl, als es normalerweise zusammen mit Rizinusöl /3-naphthylamin, 0,2 % Zinnpetroleumsulfonat und 0,2 °„Pressing, 13% mineral oil B (as stated above), 19 0 Z 0 di- (2-ethyl-hexyl) sebacate, 19% di- (3: 3: 5-trimethyl-hexyl) sebacate plus 1% di- (but-3 carbomethoxygestattet the incorporation of virtually more 35 4-oxyphenyl) thioether-cresyl phosphite, 0.5 ° / 0 phenyl-mineral oil, as it usually 3-naphthylamine together with castor oil / 0.2% Zinnpetroleumsulfonat and 0 , 2 ° "
Dimorpholinyl-phenyl-methan.Dimorpholinyl-phenyl-methane.
Das Gemisch B, "hergestellt gemäß Patent 909243, bestand aus 87,5 0Z0 Rizinusöl erster Pressung, 12,5% Mineralöl mit einer Viskosität von 44 Redwood-Sekunden bei 60c C zuzüglich2 % Di-(3-carbomethoxy-4-oxyphenyl)-thioäther-kresyl-phosphit, 10Z0 Phenyl-/3-naphthylamin, 0,2 % Zinnpetroleumsulfonat und 0,2 0Z0 Dimorpholinylphenyl-methan .The mixture B, "prepared according to Patent 909,243, consisted of 87.5 0 0 Z castor first pressing, 12.5% mineral oil having a Redwood viscosity of 44 seconds at 60 c C zuzüglich2% di- (3-carbomethoxy-4- oxyphenyl) thioether cresyl phosphite, 1 0 Z 0 phenyl / 3-naphthylamine, 0.2% tin petroleum sulfonate and 0.2 0 Z 0 dimorpholinylphenyl methane.
Dieses Öl hatte eine Viskosität von 260 Redwood-Sekunden bei 6O0C1 einen Vikositätsindex von 90 und fiel unter die SAE-Klassifikation 40.This oil had a viscosity of 260 Redwood seconds at 6O 0 C 1, a viscosity index of 90 and fell under the SAE classification 40.
verwendet werden könnte, denn der Ester wirkt als gemeinsames Lösungsmittel für beide Arten von Ölen.could be used because the ester acts as a common solvent for both types of oils.
Bei einer bevorzugten Ausführungsform der vorliegenden Erfindung kann man als Amin bzw. Zinn- und/oder Antimonverbindung Phenyl-a-naphthylamin, Phenyl-/3-naphthylamin, /3-/3-Dianaphthylamin, Di-(/3-naphthyl)-p-phenylendiamin, Phenothiazin, Benzonaphthothiazin oder Xylyl-ß-naphthylamin zusammen mit Zinnlaurat, Zinnoleat, Zinn-p-tertiärem-amyl-phenol-thio-äther oder vorzugsweise Zinn- bzw. Antimon-Petroleumsulfonat verwenden. In a preferred embodiment of the present invention can be used as amine or tin and / or Antimony compound phenyl-a-naphthylamine, phenyl- / 3-naphthylamine, / 3- / 3-dianaphthylamine, di - (/ 3-naphthyl) -p-phenylenediamine, Phenothiazine, benzonaphthothiazine or xylyl-ß-naphthylamine together with tin laurate, Tin oleate, tin-p-tertiary-amyl-phenol-thio-ether or preferably use tin or antimony petroleum sulfonate.
Mit Vorteil zu verwendende weitere Zusatstoffe sind die Triarylphosphite, insbesondere die Phosphorigsäureester aromatischer oxysubstituierter Thioäther und Disulfide, wie sie in der britischen Patentschrift 574 445 beschrieben sind, denn sie schützen nicht nur zusammengesetzte Metalle, wie z. B. Bleibronzelager, gegen Korrosion, sondern dienen auch dazu, die Belastbarkeit der Schmiermittelzusammensetzung zu erhöhen.Further additives to be used with advantage are the triaryl phosphites, in particular the phosphorous acid esters aromatic oxysubstituted thioethers and disulfides as described in British Patent 574,445 are described, because they not only protect composite metals such. B. lead bronze bearings, against corrosion, but also serve to increase the resilience of the lubricant composition.
Weitere Hilfszusatzstoffe, welche in die erfindungsgemäße Schmiermittelzusammensetzung aufgenommen werden können, sind die Reaktionsprodukte von Aldehyden oder Ketonen mit basischen wasserlöslichen primären oder sekundären Aminen, wie sie ausführlicher in der britischen Patentschrift 588 864 beschrieben sind. Ein Beispiel für eine solche Verbindung ist das Di-morpholinyl-phenyl-methan. Further auxiliary additives which are included in the inventive Lubricant compositions are the reaction products of aldehydes or ketones with basic water-soluble primary or secondary amines, as described in more detail in the British Patent 588,864. An example of such a compound is di-morpholinyl-phenyl-methane.
Falls gewünscht, können auch andere Zusatzstoffe, z. B. Reinigungsmittel (Ölschlammverhinderungsmittel) 65 und Alterungsschutzmittel, die bei hohen Temperaturen wirksam werden, vorhanden sein. So z. B. kann die Schmiermittelzusammensetzung Reinigungsmittel, wie Calciumpetroleumsulfonat oder basisches Bariumpetroleumsulfonat, oder Alterungsschutzmittel bzw. Antioxy- 70 ratur annehmen und maß dann die Reibungsleistung,If desired, other additives, e.g. B. Detergents (Oil Sludge Preventers) 65 and anti-aging agents effective at high temperatures may be present. So z. B. can the Lubricant composition detergent, such as calcium petroleum sulfonate or basic barium petroleum sulfonate, or antioxidant or antioxidant 70 and then measured the friction performance,
überzugmaß
(CRC optische
Maßung)Pistons
oversize
(CRC optical
Dimension)
gewichts
verlust
in mgcamp
weight
loss
in mg
Ölanalyse:
Prozentuale
Zunahme der
ViskositätUsed
Oil analysis:
Percentage
Increase in
viscosity
Gemisch B Mixture A
Mixture B
8,59.2
8.5
131193
131
149145
149
B. Reibungsleistung- und Öltemperatur-CharakteristikB. Frictional power and oil temperature characteristics
Die Versuche wurden ausgeführt mit einem 6-Zylinder-Chevrolet-Motor von rund 3,55 1 Zylinder volumen, angetrieben durch ein elektrisches Dynamometer unter den folgenden Verhältnissen:The tests were carried out with a 6-cylinder Chevrolet engine of around 3.55 1 cylinder volume, driven by an electric dynamometer under the following conditions:
Drehzahl:
Saugunterdruck:
Kühlwasserablauf-Temperatur :Rotational speed:
Vacuum:
Cooling water drain temperature:
3000 Umdrehungen/Minute 127 mm Hg-Säule3000 revolutions / minute 127 mm Hg column
93,3°C, wenn geben93.3 ° C when giving
nicht anders ange-not otherwise
Man ließ das Öl im Sumpf eine konstante Höchsttempe-The oil was left in the sump at a constant maximum temperature.
wobei in Abständen von 5 Minuten mindestens drei konstante Ablesungen erhalten wurden. Der Sumpf wurde dann künstlich auf 104,4 und 93,30C abgekühlt und ähnliche Ablesungen vorgenommen. Für die endgültigen Ablesungen wurde die Kühlmanteltemperatur auf 76,70C herabgesetzt und maximale Sumpfkühlung verwendet, um für jedes Öl die geringstmögliche Sumpf temperatur zu erhalten. Die Ergebnisse sind nachstehend in einer Tabelle zusammengefaßt, wobei eine besondere Spalte des Interesses halber die Viskosität des Öls bei Sumpftemperatur zeigt. at least three constant readings being obtained at 5 minute intervals. The bottom was then artificially cooled to 104.4 and 93.3 0 C and made similar readings. For the final readings the cooling jacket temperature was lowered to 76.7 0 C and maximum sump cooling used to maintain temperature the lowest possible sump for each oil. The results are summarized in a table below, with a special column for the sake of interest showing the viscosity of the oil at sump temperature .
3°3 °
Man erhielt aus den vorstehenden Versuchsergebnissen leicht, daß das Gemisch A bei den normalen Lauson- und Chevrolettesten nicht nur ein Verhalten gleichwertig dem des Gemisches B zeigte, sondern auch die Reibungsverluste sichtlich herabsetzte. Ebenso zeigte es bei den Hochtemperatur-Lausontesten eine ausgesprochene Verbesserung in bezug auf das Hängenbleiben bzw. Festbrennen der Kolbenringe.It was easily obtained from the above test results that the mixture A in the normal Lauson and Chevrolet testing not only showed a behavior equivalent to that of mixture B, but also the friction losses visibly reduced. It also showed a marked improvement in the high-temperature Lauson tests with respect to sticking or burning of the piston rings.
4040
Claims (4)
Französische Patentschrift Nr. 953 562;
USA.-Patentschriften Nr. 2 599 510, 2 570 038.Considered publications:
French Patent No. 953 562;
U.S. Patent Nos. 2,599,510, 2,570,038.
Patente Nr. 909 243, 944 748.Elderly Rights Considered:
Patents No. 909 243, 944 748.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2500/53A GB750402A (en) | 1953-01-28 | 1953-01-28 | Improvements in or relating to lubricating compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1018572B true DE1018572B (en) | 1957-10-31 |
Family
ID=9740657
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEW10942A Pending DE1018572B (en) | 1953-01-28 | 1953-04-01 | lubricant |
Country Status (6)
Country | Link |
---|---|
US (1) | US2796400A (en) |
BE (1) | BE526014A (en) |
DE (1) | DE1018572B (en) |
FR (1) | FR1092725A (en) |
GB (1) | GB750402A (en) |
MY (1) | MY5700003A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3108961A (en) * | 1959-12-21 | 1963-10-29 | Pure Oil Co | Improved anti-wear lubricating composition |
US6156228A (en) * | 1994-11-16 | 2000-12-05 | Houghton International, Inc. | Trialkoxyalkylphosphate-based fire resistant fluid containing triglyceride |
US7696136B2 (en) * | 2004-03-11 | 2010-04-13 | Crompton Corporation | Lubricant compositions containing hydroxy carboxylic acid and hydroxy polycarboxylic acid esters |
PL2467460T3 (en) * | 2009-08-18 | 2014-05-30 | Lubrizol Corp | Lubricating composition containing an antiwear agent |
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US2340073A (en) * | 1942-03-02 | 1944-01-25 | Cities Service Oil Co | Lubricating oil |
US2539504A (en) * | 1945-02-03 | 1951-01-30 | William A Zisman | Lubricating composition |
FR941250A (en) * | 1946-01-11 | 1949-01-05 | Automotive Prod Co Ltd | Castor liquid usable for energy transmission, particularly in hydraulic controls |
US2460035A (en) * | 1946-01-25 | 1949-01-25 | Standard Oil Dev Co | Synthetic lubricant |
US2499984A (en) * | 1948-12-16 | 1950-03-07 | Rohm & Haas | Oily complex esters |
US2671758A (en) * | 1949-09-27 | 1954-03-09 | Shell Dev | Colloidal compositions and derivatives thereof |
-
0
- BE BE526014D patent/BE526014A/xx unknown
-
1953
- 1953-01-28 GB GB2500/53A patent/GB750402A/en not_active Expired
- 1953-04-01 DE DEW10942A patent/DE1018572B/en active Pending
-
1954
- 1954-01-21 US US405500A patent/US2796400A/en not_active Expired - Lifetime
- 1954-01-25 FR FR1092725D patent/FR1092725A/en not_active Expired
-
1957
- 1957-12-30 MY MY3/57A patent/MY5700003A/en unknown
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FR953562A (en) * | 1944-11-10 | 1949-12-08 | Bataafsche Petroleum | Anti-rust lubricants |
US2570038A (en) * | 1948-12-29 | 1951-10-02 | Standard Oil Dev Co | Phenylenediacetate ester |
DE909243C (en) * | 1950-05-12 | 1954-04-15 | Wakefield & Co Ltd C C | lubricant |
US2599510A (en) * | 1950-12-08 | 1952-06-03 | Minshall Estey Organ Inc | Keying device for electronic organs |
DE944748C (en) * | 1952-12-10 | 1956-06-21 | Standard Oil Dev Co | lubricant |
Also Published As
Publication number | Publication date |
---|---|
US2796400A (en) | 1957-06-18 |
BE526014A (en) | |
MY5700003A (en) | 1957-12-31 |
GB750402A (en) | 1956-06-13 |
FR1092725A (en) | 1955-04-26 |
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