DE942585C - Lubricating oil - Google Patents
Lubricating oilInfo
- Publication number
- DE942585C DE942585C DEN8754A DEN0008754A DE942585C DE 942585 C DE942585 C DE 942585C DE N8754 A DEN8754 A DE N8754A DE N0008754 A DEN0008754 A DE N0008754A DE 942585 C DE942585 C DE 942585C
- Authority
- DE
- Germany
- Prior art keywords
- lubricating oil
- acid
- oil
- viscosity
- 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.)
- Expired
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
- C10M131/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen
- C10M131/08—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen containing carbon, hydrogen, halogen and oxygen
- C10M131/12—Acids; Salts or esters thereof
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts thereof
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
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- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- 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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- C10M2207/128—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 containing hydroxy groups; Ethers thereof
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- C10M2207/141—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings monocarboxylic
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- C10M2207/142—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings polycarboxylic
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- C10M2207/144—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
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- C10M2207/18—Tall oil acids
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- Chemical & Material Sciences (AREA)
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- Lubricants (AREA)
Description
AUSGEGEBEN AM 3. MAI 1956ISSUED MAY 3, 1956
N 8754 IVc 123 cN 8754 IVc 123 c
SchmierölLubricating oil
Die Erfindung bezieht sich auf Schmieröle von niedriger Viskosität mit Zusatzstoffen, welche den Ölverbrauch wirksam herabzusetzen vermögen.The invention relates to lubricating oils of low viscosity with additives which the Able to effectively reduce oil consumption.
Niedrigviskose Öle sind oft für ein wirksames •Arbeiten von Motoren, wie Verbrennungsmotoren, erwünscht oder sogar notwendig, wenn diese bei niedrigen Temperaturen arbeiten. Die Schmierung beim Anlassen und während des Laufens des Motors bei niedrigen Temperaturen ist selbst dann ungenügend, wenn SAE-io-Schmieröle für sich allein oder sogar in Mischung mit Leuchtöl verwendet werden, und man muß oft zu künstlichen Startmittelri seine Zuflucht nehmen. Die Verwendung von Ölen mit niedriger Viskosität unter solchen Bedingungen führt aber zu einem hohen Ölverbrauch und zu Korrosion.Low-viscosity oils are often essential for the effective • operation of engines, such as internal combustion engines, desirable or even necessary if these work at low temperatures. The lubrication when starting and running the engine at low temperatures is insufficient even then if SAE-io lubricating oils are used on their own or even in a mixture with luminous oil, and one must often resort to artificial starting means. The use of oils with but low viscosity under such conditions leads to high oil consumption and corrosion.
Es sind zahlreiche Mittel geprüft worden, um den Ölverbrauch herabzusetzen. Eine mechanische Abänderung der Motoren ist kostspielig und hat sich als unwirksam erwiesen. Auch die Verwendung von Viskositätsindex-Verbesserern und zahlreichen anderen Arten von Ölzusätzen hat nicht zur Lösung dieses Problems geführt.Numerous means have been explored to reduce oil consumption. A mechanical change the engine is costly and has been found to be ineffective. Also the use of Viscosity index improvers and numerous other types of oil additives did not solve this problem Problem led.
Es ist nun gefunden worden, daß der Ölverbrauch bei leichten Schmierölsorten, wie SAE-5W-Ölen, bei höheren Lauftemperaturen des Motors verringert werden kann durch Zugabe einer geringen Menge einerIt has now been found that the oil consumption with light types of lubricating oil, such as SAE-5W oils, at higher engine running temperatures can be reduced by adding a small amount of a
perfluorierten und/oder perchlorierten organischen Säure oder eines Derivates einer solchen Säure, wie eines Säurehalogenids, eines Esters, Salzes, Amids oder Imids, zu den Ölen, deren Viskosität 45 SUS bei 990 nicht überschreiten soll.perfluorinated and / or perchlorinated organic acid or a derivative of such an acid, such as an acid halide, an ester, salt, amide or imide, to the oils whose viscosity should not exceed 45 SUS at 99 0.
Diese neuen Schmiermittel eignen sich insbesondere für das Anlassen von Motoren in der Kälte, und sie weisen gleichzeitig einen Übertragungs- oder Dauereffekt auf.These new lubricants are particularly suitable for starting engines in the cold, and they have at the same time a transference or a permanent effect.
Zusätze im Sinne der Erfindung können nach irgendeiner Arbeitsweise hergestellt werden, wie sie in den USA.-Patentschriften 2 606 206, 2 567 on, 2 583 415, 2 514 473 und 2 407 315 sowie in Ind. und Eng. Chem., Bd. 43, Nr. io,.S. 2332 (1951), beschrieben sind. Die folgenden Verbindungen sind besonders gut geeignet: Perfluoressigsäure, Perfluorpropionsäure, Perfluorbuttersäure, Perfluorcaprylsäure, Perfluorcyclohexancarbonsäure, Perfluorsebazinsäure, Perfluorbutyryliluorid, Perfluorpropionylchlorid, Perfluor- no caprylamid.a-Dichlor-jö-di-fluorchlorpropionsäure, Perfluorsuccinimid usw. Gewünschtenfalls können Gemische solcher Verbindungen verwendet werden.Additives within the meaning of the invention can be prepared by any method as described in U.S. Patents 2,606,206, 2,567 on, 2,583,415, 2,514,473 and 2,407,315 and in Ind. And Eng. Chem., Vol. 43, No. io, .S. 2332 (1951). The following compounds are particularly suitable: perfluoroacetic acid, perfluoropropionic acid, perfluorobutyric acid, perfluorcaprylic acid, perfluorocyclohexanecarboxylic acid, perfluorosebazic acid, perfluorobutyryliluoride, perfluoropropionyl chloride, perfluoro- no caprylamide.
Die Zusätze gemäß vorliegender Erfindung werden zweckmäßig in Mengen von 0,01 bis 5 °/0 und vorzugsweise von etwa 0,1 bis 1 Gewichtsprozent, berechnet auf die Gesamtmischung, verwendet.The additives according to the present invention are preferably used in amounts of 0.01 to 5 ° / 0 and preferably from about 0.1 to 1 weight percent, calculated on the total mixture.
Durch die Anwendung dieser Zusätze kann der Ölverbrauch im allgemeinen mindestens um 25% und in manchen Fällen sogar um mehr als 75% herabgesetzt werden.By using these additives, the oil consumption can generally be reduced by at least 25% and in some cases can even be reduced by more than 75%.
Die erfindungsgemäßen Gemische können kleinere Mengen verschiedener üblicher Schmierölzusatzmittel enthalten, wie Mittel gegen Rosten, Korrosionsverhinderer, Mittel zur Erzeugung von Fluoreszenz, Mittel zur Herabsetzung des Stockpunktes, Reinigungsmittel, Viskositätsverbesserer, schaumhindernde Mittel und bzw. oder Mittel gegen Verschleiß. Geeignete Reinigungsmittel sind die öllöslichen Salze von metallhaltigen und/oder organischen Basen mit beispielsweise Fettsäuren von etwa 10 bis 30 Kohlenstoffatomen, wie Tallölsäuren, aus Paraffin abgeleitete Säuren (hergestellt durch Oxydation .,von festem Paraffin), aromatische Oxyfettsäuren, Benzoesäuren, welche mit Alkylgruppen, die sich von Paraffin ab-45leiten, substituiert sind, und Diphenole.The mixtures according to the invention can be smaller Contain amounts of various common lubricating oil additives, such as anti-rusting agents, corrosion inhibitors, agents for generating fluorescence, Agents to lower the pour point, cleaning agents, viscosity improvers, foam inhibitors Means and / or means against wear. Suitable cleaning agents are the oil-soluble salts of metal-containing and / or organic bases with, for example, fatty acids of about 10 to 30 carbon atoms, like tall oil acids, acids derived from paraffin (produced by oxidation., of solid Paraffin), aromatic oxy fatty acids, benzoic acids, which have alkyl groups derived from paraffin, are substituted, and diphenols.
Besonders wirksam in Verbindung mit den perhalogenierten Verbindungen gemäß der. Erfindung sind die öllöslichen Erdalkalimetall-Erdölsulfonate, insbesondere Calcium- und Bariumsulfonate, sowie die Calciumsalze von Kondensationsprodukten aus Alkylphenolen und Formaldehyd. Die metallhaltigen Reinigungsmittel werden vorteilhaft in einer Menge von etwa 0,025 bis etwa 0,2 Gewichtsprozent, bestimmt als Sulfatasche des Metallgehalts, verwendet. Geeignete Korrosionsverhinderer oder Mittel gegen Rosten sind Alkyl- oder Alkenyldicarbonsäuren mit 16 oder mehr Kohlenstoffatomen (Octadecylbernsteinsäure), Alkali- und Erdalkalisalze von Sulfonsäuren und Fettsäuren, organische Verbindungen, welche eine Säuregruppe ganz in der Nähe zu einer Nitril-, Nitro- oder Nitrösogruppe enthalten (z. B. a-Cyanstearinsäure), Glycidylphenyläther, Paraffindisulfid usw.Particularly effective in connection with the perhalogenated compounds according to. invention are the oil-soluble alkaline earth metal petroleum sulfonates, especially calcium and barium sulfonates, as well the calcium salts of condensation products of alkylphenols and formaldehyde. The metalliferous Detergents are advantageously determined in an amount of about 0.025 to about 0.2 percent by weight used as sulfated ash of the metal content. Suitable corrosion inhibitors or agents against Rusts are alkyl or alkenyl dicarboxylic acids with 16 or more carbon atoms (octadecyl succinic acid), Alkali and alkaline earth salts of sulfonic acids and fatty acids, organic compounds, which contain an acid group very close to a nitrile, nitro or nitroso group (e.g. a-cyanosearic acid), Glycidyl phenyl ether, paraffin disulfide, etc.
Je nach dem Zusatzstoff und den Bedingungen, unter welchen das Öl verwendet wird, kanm die Menge des verwendeten Zusatzes zwischen 0,01 mud 2 Gewichtsprozent oder darüber liegen, wesenflciie Verbesserungen werden jedoch mit Mengen im. Bereich von 0,1 bis 0,5 Gewichtsprozent erzielt.The amount can vary depending on the additive and the conditions under which the oil is used of the additive used are between 0.01 and 2 percent by weight or more, there are significant improvements however, with quantities in the. Range of 0.1 to 0.5 percent by weight achieved.
Die Grundöle, mit welchen die Zusätze, gemäß vorliegender Erfindung kombiniert werden, sind leichte Schmieröle mit einer Saybolt-Universal-Viskositä.t bei 98,9° von .nicht über 45.Sekunden. Es können natürliche und synthetische Öle, wie Ester vom Polycarbonsäuren, Polyalkylenoxyde, organische flüssige Silicone usw. sowie auch Gemische derselben verwendet werden. Ein typisches Öl dieser Art ist ein mineralisches SAE-5W-Motorschmieröl mit folgenden Eigenschaften:The base oils with which the additives are combined in accordance with the present invention are light ones Lubricating oils with a Saybolt Universal viscosity at 98.9 ° of not more than 45 seconds. It can natural and synthetic oils, such as esters of polycarboxylic acids, polyalkylene oxides, organic liquids Silicones etc. as well as mixtures thereof are used will. A typical oil of this type is SAE 5W mineral engine lubricating oil with the following Characteristics:
Flammpunkt 196,I0 Flash point 196, I 0
Fließpunkt .— I2,3a Flow point .— I2.3 a
Viskosität SUS bei 98,9° . 39,7Viscosity SUS at 98.9 °. 39.7
Viskositätsindex 95Viscosity index 95
Zusatzstoffe gemäß vorliegender Erfindung sind bezüglich der Herabsetzung des ölverbrauches tuik wirksam bei Ölen, die eine höhere Viskosität als die oben angegebene aufweisen.Additives according to the present invention are useful in terms of reducing oil consumption effective with oils that have a viscosity higher than that specified above.
Die folgenden Beispiele erläutern die Erfindung näher, wobei die Angabe »SAE-sW-Motoröltf ein Öl bezeichnet, welches die vorstehend angegebenen Eigenschaften besitzt.The following examples explain the invention in more detail, where the indication »SAE-sW-Motoröltf an oil denotes which has the properties given above.
Beispiel 1 GewichtsExample 1 weight
prozentpercent
Perfluorcaprylamid 0,2 °/0 Perfluorcaprylamid 0.2 ° / 0
SAE-5W-Motoröl RestSAE 5W engine oil rest
Perfluorcaprylsäure 0,2 °/0 Perfluorocaprylic acid 0.2 ° / 0
SAE-5W-Motoröl RestSAE 5W engine oil rest
Perfluorsebazinsäure 0,1 °/0 Perfluorsebazinsäure 0.1 ° / 0
SAE-5W-Motoröl RestSAE 5W engine oil rest
Perfluorcaprylamid 0,2 °/0 Perfluorcaprylamid 0.2 ° / 0
Calciumerdöbnahagonisulfonat 0,4% (SA)Calcium Erdöbnahagonisulfonat 0,4% (SA)
SAE-5W-Motoröl RestSAE 5W engine oil rest
Perfluorcaprylamid 0,2 °/0 Perfluorcaprylamid 0.2 ° / 0
Calciumsalz des Octylphenol-Formaldehyd-Kondensationsproduktes mit einem durchschnittlichen Gehalt von etwa 5 Phenoleinheiten je Molekül ... 0,3 % (SA)Calcium salt of the octylphenol-formaldehyde condensation product with an average content of about 5 phenol units per molecule ... 0.3% (SA)
SAE-5W-Motoröl RestSAE 5W engine oil rest
Beispiel 6 laa Example 6 laa
Perfluorcaprylsäure 0,2 °/0 Perfluorocaprylic acid 0.2 ° / 0
Calcium-Erdöhnahagonisulfonat ...... 0,1 % (SA)Calcium-Erdöhnahagonisulfonat ...... 0.1% (SA)
Calciumsalz eines Octylphenol-Formaldehyd-Kondensationsproduktes Calcium salt of an octylphenol-formaldehyde condensation product
(Molgewicht 980 bis 1500) 0,3 % (SA)(Molecular weight 980 to 1500) 0.3% (SA)
SAE-5W-Motoröl RestSAE 5W engine oil rest
Beispiel 7 GewichtsExample 7 weight
prozentpercent
a-Dichlor-yS-difluorchlorpropionsäure ... 0,1 °/0 a-dichloro-yS-difluorochloropropionic acid ... 0.1% / 0
SAE-5W-Motoröl RestSAE 5W engine oil rest
Perfluorcaprylamid 0,3 °/oPerfluorocaprylamide 0.3%
Polyalkylenoxyde (SUS bei 990 Polyalkylene oxides (SUS at 99 0
41 Sekunden) Rest41 seconds) rest
Perchloracetamid 0,1 %Perchloracetamide 0.1%
Perfluormyristinsäure 0,2 °/0 Perfluormyristinsäure 0.2 ° / 0
SAE-5W-Motoröl RestSAE 5W engine oil rest
Acetamid 0,1 °/oAcetamide 0.1%
Perfluorbernsteinsäureimid 0,2 %Perfluorosuccinic acid imide 0.2%
SAE-5W-Motoröl RestSAE 5W engine oil rest
Perfluorcaprylamid 0,3 %Perfluorocaprylamide 0.3%
Calciumerdölmahagonisulfonat 0,1 % ICalcium Petroleum Mahogany Sulphonate 0.1% I.
Calciumsalz eines Octylphenol-Forma5 aldehyd-KondensationsproduktesCalcium salt of an octylphenol form a 5 aldehyde condensation product
(Molgewicht 980 bis 1500) 0,3 % (SA)(Molecular weight 980 to 1500) 0.3% (SA)
SAE-5W-Motoröl RestSAE 5W engine oil rest
In den vorstehenden Beispielen bedeutet »SA« »bestimmt als Sulfatasche«.In the examples above, "SA" means "determined to be sulfated ash".
Außer der Herabsetzung des Ölverbrauchs besitzen die erfindungsgemäßen Gemische auch die vorteilhaften Eigenschaften, daß sie einen Übertragungsoder Dauereffekt aufweisen. So zeigen Motoren, welchen erfindungsgemäße Gemische zugeführt oder welche mit solchen in Betrieb gehalten worden sind, eine Übertragungswirkung, nachdem diese entfernt worden sind und der Motor mit normalen mineralischen Destillatölen oder mit anderen handelsüblichen Schmierölen mit niedriger Viskosität betrieben wird. Um nachzuweisen, daß die erfindungsgemäßen Gemische tatsächlich einen verringerten Ölverbrauch herbeiführen, wurden mehrere Gemische verschiedenen Prüfungen unterworfen. Die Ergebnisse sind in der nachstehenden Tabelle I zusammengestellt. Sie sind ausgedrückt in Prozent der Herabsetzung des Ölverbrauchs im Vergleich zum Ölverbrauch bei Verwendung des Grundöls ohne Zusatzstoff.In addition to reducing the oil consumption, the mixtures according to the invention also have the advantageous ones Properties that they have a transmission or persistence effect. Motors show which mixtures according to the invention have been supplied or which have been kept in operation with such, a transfer effect after these have been removed and the engine with normal mineral Distillate oils or other commercially available lubricating oils with low viscosity is operated. To prove that the mixtures according to the invention actually have a reduced oil consumption induce, several mixtures were subjected to different tests. The results are compiled in Table I below. They are expressed as a percentage of the reduction the oil consumption compared to the oil consumption when using the base oil without additives.
Herabsetzung im Ölverbrauch, ProzentReduction in oil consumption, percent
Das Gemisch X bestand aus dem gleichen Grundöl, wie es bei den vorhergehenden Gemischen verwendet worden war, zu welchem eine solche Menge »Acryloid 710« zugesetzt worden war, daß die Viskosität auf SAE ioW erhöht wurde.Mixture X consisted of the same base oil as used in the previous mixes to which such an amount of "Acryloid 710" had been added that the viscosity increased to SAE ioW was increased.
»Acryloid 710« ist ein Alkylmethacrylat-Polymeres mit folgenden Eigenschaften:»Acryloid 710« is an alkyl methacrylate polymer with the following properties:
Spezifisches Gewicht, °API 27Specific weight, ° API 27
Spezifisches Gewicht 15,6/15,6° .0.89Specific gravity 15.6 / 15.6 ° .0.89
Flammpunkt 204,4°Flash point 204.4 °
Fließpunkt — 6,7°Pour point - 6.7 °
Viskosität (SUS bei 37,8°) 2400Viscosity (SUS at 37.8 °) 2400
Farbe ASTM 2Color ASTM 2
Neutralisationszahl 0,3Neutralization number 0.3
Das Gemisch Y bestand aus einem SAE-30-Motoröl + 0,2 °/0 Perfluorcaprylamid. Das Motoröl in dieser Zusammensetzung wurde aus einem Westtexas-Ellenberger-Rohöl erhalten durch Destillation, Entasphaltieren, Lösungsmittelextraktion und Entparaffinieren und hatte die folgenden Eigenschaften:The mixture consisted of a Y SAE-30 motor oil + 0.2 ° / 0 Perfluorcaprylamid. The motor oil in this composition was obtained from a West Texas-Ellenberger crude by distillation, deasphalting, solvent extraction and dewaxing and had the following properties:
Spezifisches Gewicht, 0API 25,3Specific gravity, 0 API 25.3
Flammpunkt 'COC 221,1°Flash point 'COC 221.1 °
Viskosität (SUS bei 98,9°) 630Viscosity (SUS at 98.9 °) 630
Viskositätsindex 50Viscosity index 50
Nach dem CRC-L-4-Test, der im Buch »Motor Oils and Engine Lubrication« von Carl W. Georgi (Reinhold Publ. Corp.) auf Seite 67 bis 72 beschrieben ist, wird ein 6-Zylinder-Chevrolet-Motor 1942 (Bohrung 8,89 cm, Hub 9,525 cm, Kompressionsverhältnis 6,5 :1) 36 Stunden mit 3150 Umdrehungen pro Minute und einer Belastung von 30,42 Brems-PS in Betrieb gehalten.According to the CRC-L-4 test described in the book "Motor Oils and Engine Lubrication" by Carl W. Georgi (Reinhold Publ. Corp.) on pages 67 to 72, a 6-cylinder Chevrolet engine is 1942 (bore 8.89 cm, stroke 9.525 cm, compression ratio 6.5: 1) 36 hours at 3150 revolutions per minute and a load of 30.42 brake horsepower kept in operation.
Nach dem FL-2-Test, der im gleichen Buch auf Seite 366 bis 367 beschrieben ist, läßt man dieselbe Maschine 40 Stunden bei 2500 Umdrehungen je Minute und einer Belastung von 45,62 Brems-PS laufen, und der Ölverbrauch wird bestimmt durch Abziehen des Öles in bestimmten Zeitabständen (10 Stunden) und Messen der Ölmenge.After the FL-2 test described on pages 366 to 367 of the same book, the same is left Machine 40 hours at 2500 revolutions per minute and a load of 45.62 brake horsepower run, and the oil consumption is determined by drawing off the oil at certain time intervals (10 hours) and measuring the amount of oil.
Bei einem anderen CRC-L-4-Test ließ man den Motor mit dem im Beispiel 2 angegebenen Schmiermittel laufen; es wurde eine Herabsetzung im Ölverbrauch um etwa 60% festgestellt. Das Öl wurde entfertit und der Motor dann mit dem Grundöl ohne Zusatz in Betrieb gehalten. Es wurde eine Herabsetzung im Ölverbrauch von rund 25% festgestellt, wodurch die Ubertragungswirkung der vorliegenden Erfindung gezeigt ist.In another CRC-L-4 test, the engine was left with the lubricant specified in Example 2 to run; a reduction in oil consumption of about 60% was found. The oil was Entfertit and the engine is then kept in operation with the base oil without any additives. It became a disparagement found in oil consumption of around 25%, thus reducing the transfer effect of the present Invention is shown.
Gemische gemäß vorliegender Erfindung setzen nicht nur den Ölverbrauch wesentlich herab, sondern sie verhindern auch die Abnutzung, Korrosion sowie Schlamm- und Lackbildung. Die erfindungsgemäßen Schmiermittel sind auch besonders geeignet beim Anlassen und ersparen die Notwendigkeit eines Anwärmens des Motors.Mixtures according to the present invention not only significantly reduce oil consumption, but also they also prevent wear, corrosion, and sludge and varnish build-up. The invention Lubricants are also particularly useful in starting and save the need for one Warming up the engine.
Claims (3)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US348806A US2715107A (en) | 1953-04-14 | 1953-04-14 | Lubricating compositions |
Publications (1)
Publication Number | Publication Date |
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DE942585C true DE942585C (en) | 1956-05-03 |
Family
ID=23369618
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEN8754A Expired DE942585C (en) | 1953-04-14 | 1954-04-13 | Lubricating oil |
Country Status (4)
Country | Link |
---|---|
US (1) | US2715107A (en) |
DE (1) | DE942585C (en) |
FR (1) | FR1097961A (en) |
GB (1) | GB752383A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1107867B (en) * | 1959-02-06 | 1961-05-31 | Exxon Research Engineering Co | Mineral lubricating oil |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2915471A (en) * | 1956-04-16 | 1959-12-01 | Shell Dev | Lubricating oil compositions |
US2977306A (en) * | 1958-03-31 | 1961-03-28 | California Research Corp | Lubricant composition |
US3226323A (en) * | 1963-04-30 | 1965-12-28 | Monsanto Res Corp | Lubricant composition containing a haloalkanoic compound |
US3269948A (en) * | 1963-08-30 | 1966-08-30 | Exxon Research Engineering Co | Amine salts of perhalogenated monobasic carboxylic acids |
US3284355A (en) * | 1963-09-12 | 1966-11-08 | Mobil Oil Corp | Lubricating compositions |
US3329611A (en) * | 1965-03-17 | 1967-07-04 | Sinclair Research Inc | Lubricating oil composition |
US3436348A (en) * | 1966-10-20 | 1969-04-01 | Sinclair Research Inc | Ester base lubricating oil containing a stabilizing mixture of alkali metal organic compound and an aromatic amine |
US4079012A (en) * | 1976-10-04 | 1978-03-14 | Bosniack David S | Synthetic ester oil compositions containing organic sulfonic acid ammonium salts as load-carrying agents |
EP0004957A3 (en) * | 1978-04-26 | 1980-04-16 | Ciba-Geigy Ag | Compositions and use of chlorinated derivatives of butyric acid as additives for lubricants |
US5182039A (en) * | 1991-03-29 | 1993-01-26 | Exxon Chemical Patents, Inc. | Synergistic fluorinated ore flotation aids |
WO2000020539A1 (en) * | 1998-10-02 | 2000-04-13 | E.I. Du Pont De Nemours And Company | Additive for lubricants |
US6642186B2 (en) | 1998-10-02 | 2003-11-04 | E. I. Du Pont De Nemours And Company | Additive for lubricants |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2411159A (en) * | 1943-07-22 | 1946-11-19 | Du Pont | Lubricant |
NL66836C (en) * | 1943-09-15 | |||
US2606212A (en) * | 1944-07-28 | 1952-08-05 | Purdue Research Foundation | Perfluoro-alkyl-cyclohexanes |
US2456176A (en) * | 1944-12-30 | 1948-12-14 | Du Pont | Monomeric addition products of azobisformates and polyfluoroethylenes |
US2567011A (en) * | 1949-01-10 | 1951-09-04 | Minnesota Mining & Mfg | Fluorocarbon acids and derivatives |
US2616927A (en) * | 1950-05-12 | 1952-11-04 | Minnesota Mining & Mfg | Fluorocarbon tertiary amines |
US2680717A (en) * | 1953-02-12 | 1954-06-08 | Du Pont | Salts of polymeric amines with perfluorocarboxylic acids |
-
1953
- 1953-04-14 US US348806A patent/US2715107A/en not_active Expired - Lifetime
-
1954
- 1954-04-12 FR FR1097961D patent/FR1097961A/en not_active Expired
- 1954-04-12 GB GB10683/54A patent/GB752383A/en not_active Expired
- 1954-04-13 DE DEN8754A patent/DE942585C/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1107867B (en) * | 1959-02-06 | 1961-05-31 | Exxon Research Engineering Co | Mineral lubricating oil |
Also Published As
Publication number | Publication date |
---|---|
US2715107A (en) | 1955-08-09 |
GB752383A (en) | 1956-07-11 |
FR1097961A (en) | 1955-07-13 |
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