DE1594427A1 - lubricant - Google Patents
lubricantInfo
- Publication number
- DE1594427A1 DE1594427A1 DE1966E0030908 DEE0030908A DE1594427A1 DE 1594427 A1 DE1594427 A1 DE 1594427A1 DE 1966E0030908 DE1966E0030908 DE 1966E0030908 DE E0030908 A DEE0030908 A DE E0030908A DE 1594427 A1 DE1594427 A1 DE 1594427A1
- Authority
- DE
- Germany
- Prior art keywords
- lubricant according
- lubricant
- plus
- thickener
- metal
- 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.)
- Granted
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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
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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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
- 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
- C10M2207/046—Hydroxy ethers
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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
- 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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- 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
- 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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- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- 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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- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/146—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings having carboxyl groups bound to carbon atoms of six-membeered aromatic rings having a hydrocarbon substituent of thirty or more carbon atoms
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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
- 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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- 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
- 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
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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
- 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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- 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
- 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
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
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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
- 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
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
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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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/06—Groups 3 or 13
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/08—Groups 4 or 14
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
(Britisch 8013/65 - prio 24.2.1965 - 4056)(British 8013/65 - prio 24.2.1965 - 4056)
Bsso Research and
Engineering CompanyBsso Research and
Engineering Company
Die vorliegende Erfindung betrifft Schmiermittel und Inebesondere Schmiermittel, welche mit einen Llthlunaalz einer Fettsäure, inabesondere Lithium-12-hydroxystearat, verdiokt sind.The present invention relates to lubricants and more particularly Lubricant which is diluted with an oil salt of a fatty acid, in particular lithium-12-hydroxystearate are.
Schmiermittel mit gutem Gebrauchewert bei hohen Temperaturen sind bekannt. Derartige Schalermittel bestehen aus einen Orundöl wie einen raffinierten jKefetenwasserstoffOl von Schmiermittelqualltlt, einem Verdickungsmittel wie einem FettsKuresalz oder einer Fettsäureseife oder eine« nicht seifenartigen Verdickungsmittel, gegebenenfalls «inen» polaren Strukturmodlflkator ftir da» Verdickungsmittel, s.B« Olyoerin, und gebräuchlichen Zusatzstoffen sxtr Verbesserung der Oxydatlonsbeetändlgkeit, der Hochdruokeigensohaften und/oder der Korrosionsbeständigkeit. Derartige Zusatzstoffe sind beispielsweise Diarylamlne wie Phenyl- oC naphthylamln zur Srhöhung der Oxydatlonsbestttndigkeit, Metallalkyl- oder -arylthicphosphate wie Zink-oder Cadniue-Lubricants with good utility value at high temperatures are known. Such Schalermittel consist of a Orundöl as a refined jKefetenwasserstoffOl of Schmiermittelqualltlt, a thickening agent such as a FettsKuresalz or a fatty acid soap or a "non-soap thickener, if necessary," inen "polar Strukturmodlflkator FTIR as" thickening agents, SB "Olyoerin, and conventional additives sxtr improve Oxydatlonsbeetändlgkeit , the high pressure properties and / or the corrosion resistance. Such additives are, for example, diarylamines such as phenyl naphthylamine to increase the resistance to oxidation, metal alkyl or arylthic phosphates such as zinc or cadnium phosphates
909821/0949 BAD ORIGINAL909821/0949 BATH ORIGINAL
dialkyldithiophosphat zur gleichzeitigen Verbesserung der OxydatlonsbestHndlgkeit und der Hochdruckeigeneohaften und Metallnaphthenate wie Bleinaphthenat zur Verbesserung der korrosIonsverhütenden Eigenschaften. Bisher war es jedoch nioht möglich, eine befriedigende Kombination aller dieser Eigenschaften zu erzielen.dialkyldithiophosphate to simultaneously improve the Oxidation resistance and the high pressure properties and metal naphthenates such as lead naphthenate for improvement the anti-corrosive properties. So far it was however not possible a satisfactory combination of all to achieve these properties.
Mit der vorliegenden Erfindung soll nun ein Schmiermittel vorgeschlagen werden, welches einen guten Gebrauchswert bei hohen Temperaturen, gute Hochdruckelgonschaften, eine gute Rostschutzwirkung und gute abnutzungsverhllgende Eigenschaften aufweist. Weiterhin soll mit der Erfindung ein Schmiermittel vorgeschlagen werden, welches auf neugespritzten Fliehen keine Flecken hinterläßt.The present invention is now intended to provide a lubricant be proposed, which has a good utility value at high temperatures, good high-pressure Elgonschaften, a good anti-rust effect and good anti-wear properties having. Furthermore, a lubricant is to be proposed with the invention, which on newly sprayed Fleeing does not leave stains.
Das erflndungsgemäße Schmiermittel enthält ein QrundÖl, ein Verdickungsmittel, ein MctaXldialkylthiophosphat oder Metalldiarylthiophosphat oder Metallmonoalkylmonoarylthiophosphat, Salicylsäure oder ein Metallsalz der Salicylsäure und eine öllösliche alkylsubstltuierte Arylsulfonsiiure oder ein Metallsalz derselben.The lubricant according to the invention contains a basic oil, a thickener, a MctaXldialkylthiophosphat or Metal diaryl thiophosphate or metal monoalkyl monoaryl thiophosphate, Salicylic acid or a metal salt of salicylic acid and an oil-soluble alkyl-substituted arylsulfonic acid or a Metal salt thereof.
Das Verdickungsmittel besteht vorzugsweise aua einer liithlumseife oder einem Lithiumsalz einer Fetfcsliure, insbesondere Lithium-12-hydroxystearat, welches dom Schmier-The thickening agent preferably consists of one Lithium soap or a lithium salt of a fatty acid, in particular Lithium-12-hydroxystearate, which is a lubricant
mittel in einer Menge tugesatct wird, welche die erforderlicheagent is tugesatct in an amount which the required
909821/0949 BAD ORIGINAL909821/0949 BATH ORIGINAL
!Consistent ergibt. Als Verdickungsmittel lcBnnen auch Aluminlumkoeplexeeifen verwendet werden. Ia allgemeinen wird das Lithlum-12-hydroxyetearat, bezogen auf die Oe- «aatmenge Orundul plus Verdickungsmittel, in einer Menge von etwa ? bl« 12 Gew.Jf verwendet. Die bevorzugte Menge liegt» bezogen auf die Gesamtaenge Orundöl plus Verdickungsmittel, zwischen 9 und H Gew. Ji, jedoch ktanen in «anohen Fällen auch bis herunter zu 1 Oew.Jf und bis herauf zu 15 Gew. Ji verwendet werden« Bei Verwendung einer Alumlnlumkoaplexverblndung liegt die entsprechend· Menge vorzugsweise zwischen 6 und 12 Oew.Jf. Oegeboiienfalls kann das Sclimierraittel mit elnooi polaren Strukturoodiflkator wie beispielsweise Glycerin in einer auf da3 Verdickvingsmittel bezogenen Menge von bis zu 25 Oew.#, s.B. von 5 bis 25 Gew.%t oder in einer auf das Gesamtprodukt bezogenen Menge von bis zu 4 Gew.%, z.3. 0,5 bis 4 Gew.Je, versetzt worden. Außer Glycerin können als polare Strukturnodifikatoren Dl- und Polyhydroxyverbindungen verwendet werden, bei welchen sich die Hydroxylgruppen an zwei benachbarten oder durch höchstens ein Kohlenstoffatom getrennten Kohlenstoffatomen befinden. Die Strukturnodifikatoren umfassen also eine große Zahl von Diolen oder Polyalkohole!! sowie Uthoxylierta Derivate von Fettalkoholen, Fettsäuren oder Diolen.! Consistent results. Aluminum complexes can also be used as thickening agents. In general, the lithium 12-hydroxyetearate, based on the amount of oil orundul plus thickener, is used in an amount of about? Bl «12 Gew.Jf used. The preferred amount is "based on the total amount of orund oil plus thickener, between 9 and 1 wt. Ji, but in" abnormal cases down to 1 ow.Jf and up to 15 wt the corresponding amount is preferably between 6 and 12 ow.Jf. Oegeboiienfalls the Sclimierraittel can with elnooi polar Strukturoodiflkator such as glycerol in a related da3 Verdickvingsmittel amount of up to 25 OEW. # SB from 5 to 25 wt.% T or in a related to the total amount of product of up to 4 wt.% , z.3. 0.5 to 4 percent by weight each has been added. In addition to glycerol, Dl and polyhydroxy compounds can be used as polar structure modifiers in which the hydroxyl groups are located on two adjacent carbon atoms or separated by at most one carbon atom. The structure modifiers thus include a large number of diols or polyalcohols! and Uthoxylierta derivatives of fatty alcohols, fatty acids or diols.
909821/0949 BAD ORIGINAL909821/0949 BATH ORIGINAL
159U27159U27
Dae Metalldialkyl- oder -diarylthiophosphat besteht vorzugsweise aus einen öllöslichen Zinkdlalkyldlthiophosphat, in welchem die Alkylgruppen gleich oder verschieden sein können. Bevorzugt werden Zink-isobutyl-ainyl-dithlophosphat und Zink-Kthylisobutyl-isopropyl-dithiophosphat. Diese Thiophosphate werden vorzugsweise in auf die Gesamtmenge Grundöl plus Verdickungsmittel plus gegebenenfalls polarem Strukturraodifilcator bezogenen Mengen von 0,2 bis 5,0 0ew.£ eingesetzt. Anstelle eines Dialkyl- oder Dlarylthlophosphats kann auch ein Metall-monoalkyl-monoaryl-thiophospnat, z.B. Zink-Isobutyl-phenyl-dithiophosphat, verwendet werden. Das ThIophosphat muß dabei vollständig verestert sein, so daß die beiden Kohlenwasserstoffreste an den Sauerstoffatomen im Thlophosphatrest entweder beide aus Alkylresten oder beide aus Arylresten oder einem Alkyl- und einem Arylrest bestehen.The metal dialkyl or diaryl thiophosphate is preferably made from an oil-soluble zinc-alkyl-thiophosphate, in which the alkyl groups can be identical or different. Zinc isobutyl aynyl dithlophosphate and Zinc ethyl isobutyl isopropyl dithiophosphate. These thiophosphates are preferably added to the total amount of base oil plus thickener plus, if necessary, a polar structural detergent related quantities of 0.2 to 5.0 wt. £ are used. Instead of a dialkyl or Dlarylthlophosphat can also a metal monoalkyl monoaryl thiophosphate, e.g. zinc isobutyl phenyl dithiophosphate, be used. The thiophosphate must be completely esterified so that the two hydrocarbon radicals on the oxygen atoms in the thlophosphate radical, either both from alkyl radicals or both consist of aryl radicals or an alkyl and an aryl radical.
Bei der bevorzugten AusfUhrungsform der Erfindung wird ein Salicylsauresalζ zugesetzt, lnebesondero Bleisalioylat, Jedoch können auch ändere Salz« wie Mono- oder Dilithiutn-' sallxylat oder freie Salioyls8.ure verwendet werden. Die bevorzugte Menge Salicylsäure oder Salicylat betragt, bezogen auf die Gesamtmenge Qrundöl plus Verdickungsmittel plus gegebenenfalls polarem Strukturmodifikator, 0,1 bis 5,0 0ew.£ und vorzugsweise 0,25 bis 4,0 Gew.#.In the preferred embodiment of the invention, a Salicylic acid salt added, lnebesondero lead salioylate, however can also use other salt «such as mono- or dilithiutn- ' sallxylat or free salioyls8.ure can be used. The preferred one Amount of salicylic acid or salicylate is based on the total amount of base oil plus thickener plus optionally polar structure modifier, 0.1 to 5.0 wt. £ and preferably 0.25 to 4.0 wt. #.
909821/0949909821/0949
BAD ORIGINALBATH ORIGINAL
• . · ... ' 159U27 " -5-•. · ... '159U27 " -5-
Yorsugswelse wird noch ·1η 8 Is einer ullBeliohen alkyl* substitulerten Aryleulfonsture, insbesondere «In Brdalkallsalas einer alkyleubetituierten Naphtha! InmilfonsMura «It 2 bis 28 Kohlenstoffatom J· Alkylrtet In ·1μγ atif dl· OesaatMoge Orundöl plus Verdiotamgiaittel plus gtgebenwifalle polar·« Strukturmodlfllcatop btxogtnen Nmg· von 0,1 bi· 5,0 Ctew.jf *ue#e*tit. Bevoriugt werden Barluouals·, Jedoch können gegebenenfalls auch andere Saite wie Calolut- oder HegnesiuBÄUlfonate oder Alkallsalie oder freie AiIfon- «Küre oder Jtelnialse derselben In Iqulvalenten Mengen verwendet werden·Yorsugswelse is still 1η 8 Is a ullBeliohen alkyl * substituted aryl sulfonic acid, especially «In Brdalkallsalas an alkyl substituted naphtha! InmilfonsMura «It 2 to 28 carbon atoms J Alkylrtet In 1μγ atif dl OesaatMoge Orundöl plus Verdiotamgiamittel plus gtgendwifalle polar · «Structural modulatop btxogtnen Nmg · of 0.1 bi5.0 Ctew.jf * ue # e * tit. Barluouals are preferred, however other strings such as calolut can also be used or HegnesiuBÄUlfonate or Alkallalie or free AiIfon- «Küre or Jtelnialse of the same in Iqulvalent quantities be used·
Die Erfindung wird durch die folgenden Beispiele nlher erlSutert· 'The invention is explained in more detail by the following examples: '
Beispiele 1-25Examples 1-25
Komponenten unter dem Fachmann gelluf igen Heratellungsbedingungen für derartige Sohnlermittel vermischtιComponents under preparation conditions known to those skilled in the art for such sonic agents mixed
Orundöl (1) 87,57Orund oil (1) 87.57
(1) mit Lusungsmittel extrahiertes Naphthenkohlenwaseerstofföl mit* elier Viskosltllt von 450 Saybolt-Sekunden bei 37,0° C.(1) Naphthenic hydrocarbon oil extracted with solvent with an * elier viscosity of 450 Saybolt seconds at 37.0 ° C.
909821/0949909821/0949
BAD ORIGINALBATH ORIGINAL
AuT diese Weise vurde ein Schmiermittel erhalten, welches mit etwa 10 Oew.jG Lithium-12-hydroxystearat verdickt war.In this way a lubricant was obtained which was thickened with about 10 Oew.jG lithium 12-hydroxystearate.
Dieses Schmiermittel wurde mit verschiedenen Mengen von (A) Zinkdialkyldlthlophosphat, in welchem der eine Alkylrest aus einem Ioobutylrest und der andere aus einem Amylrest bestand, (B) Blelsalioylat und (C) Bar iumdi(nonylnaph thai Insulfonat) versetzt; die erhaltenen Schmiermittel wurden den folgenden Testen unterworfent .This lubricant was made with various amounts of (A) Zinc dialkyldlthlophosphate, in which the one alkyl radical from an ioobutyl residue and the other from an amyl residue consisted of (B) blelsalioylate and (C) bar iumdi (nonylnaph thai insulfonate) offset; the obtained lubricants were subjected to the following tests.
ASTH-Method· D 9*2; der Druckabfall wurde nach 100 Stun» den gemessen.ASTH-Method · D 9 * 2; the pressure drop was after 100 hours the measured.
Timken-Bslastungstest (H) (Timken Load Test) Fed. M. 791 - 6505 Timken Load Test (H ) Fed. M. 791-6505
Wear; Teet)Wear; Tea)
gMCOn-Korroslonstest gMCOn corrosion test (U)(U)
DIN-Methode 5 l302; die Korrosion wurde naoh f und in einigen Fällen nach 12 und 21 Tagen gemessen.DIN method 5 1302; the corrosion was naoh f and in some cases measured after 12 and 21 days.
SKF-Test·. bei hoher Temperatur (V) SKF test ·. at Hoh he Te m perature (V)
DHI-Mothode 5 l806, auf 23 Togo ausgedehnt.DHI-Mothode 5 1806, extended to 23 Togo.
909821/0949909821/0949
BAD ORIGINALBATH ORIGINAL
159U27159U27
Die Ergebniese dieser Teste sind in der nachfolgenden Tabelle zusammengestellt.The results of these tests are shown below Table compiled.
Au« der Tabelle geht hervor, daß bei alleiniger Verwendung eines Zlnkdlalkyldlthiophosphats zwar gute Hochdruokelgensohaften und gute Abnutzungsbestandigkelt erzielt werden» gute Oxidationsbeständigkeit, gute Korrosionsbeständigkeit und gute Eigenschaften bei hohen Temperaturen Jedoch erst entwickelt werden« wenn man ein Salicylat .und ein Alkylarylsulfonat zusetzt. Diese Ergebnisse sind insofern beattrtcenitoert, als die Koribination der Wirkungen der drei Zusatzstoffe ohne nachteilige Auswirkung auf die anderen Eigenschaften des Sohmiernittels erzielt wird. Darüber hinaus hinterläSt das die drei Zusatzstoffe enthaltende Sobnleraittel kein· Flecken auf neu gespritzten Flächen von AutokaroBMrleZi oder dergleichen.The table shows that when used alone Zlnkdlalkyldlthiophosphats good Hochdruokelgensohaften and good wear resistance can be achieved » good oxidation resistance, good corrosion resistance and good properties at high temperatures be developed «if you have a salicylate. and an alkylarylsulfonate clogs. These results are beattrtcenitoert insofar as as the correlation of the effects of the three Additives with no adverse effect on the others Properties of the Sohmiernittels is achieved. About that In addition, the Sobnlera agent containing the three additives does not leave any stains on newly sprayed surfaces AutokaroBMrleZi or the like.
909821/0949909821/0949
BAD ORIGINALBATH ORIGINAL
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, , CM UNUNO «ΛΟ O O C?tOO,, CM UNUNO «ΛΟ O O C? TOO
Claims (12)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8013/65A GB1089463A (en) | 1965-02-24 | 1965-02-24 | Improvements in or relating to grease compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1594427A1 true DE1594427A1 (en) | 1969-05-22 |
Family
ID=9844110
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1966E0030908 Granted DE1594427A1 (en) | 1965-02-24 | 1966-01-22 | lubricant |
Country Status (3)
Country | Link |
---|---|
US (1) | US3493507A (en) |
DE (1) | DE1594427A1 (en) |
GB (1) | GB1089463A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3981810A (en) * | 1975-11-11 | 1976-09-21 | The United States Of America As Represented By The Secretary Of The Navy | Grease composition |
JPS6346299A (en) * | 1986-01-16 | 1988-02-27 | Ntn Toyo Bearing Co Ltd | Grease for constant speed joint |
US4822505A (en) * | 1987-07-31 | 1989-04-18 | Exxon Research And Engineering Company | Load-carrying grease |
US5672572A (en) * | 1993-05-27 | 1997-09-30 | Arai; Katsuya | Lubricating oil composition |
JP3402407B2 (en) * | 1994-10-05 | 2003-05-06 | 昭和シェル石油株式会社 | Grease for tripod type constant velocity joint |
US20050197260A1 (en) * | 2004-02-05 | 2005-09-08 | Montana State University | Environmentally friendly grease composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2364283A (en) * | 1941-10-21 | 1944-12-05 | Union Oil Co | Modified lubricating oil |
US2944970A (en) * | 1954-07-12 | 1960-07-12 | Shell Oil Co | High temperature grease compositions containing salicylic acid derivatives |
US2837549A (en) * | 1955-05-12 | 1958-06-03 | American Cyanamid Co | Zinc dialkyl dithiophosphates |
US2951808A (en) * | 1957-12-31 | 1960-09-06 | Exxon Research Engineering Co | Lubricant compositions containing metal salts of aromatic hydroxy carboxylic acids as antioxidants |
US3075005A (en) * | 1959-10-05 | 1963-01-22 | Continental Oil Co | Production of dinonylnaphthalene sulfonates |
US3015623A (en) * | 1960-06-24 | 1962-01-02 | Sinclair Refining Co | Lithium base grease containing lead oleate, sulfurized lard oil and molybdenum disulfide |
US3203897A (en) * | 1962-09-20 | 1965-08-31 | Gulf Research Development Co | Sodium soap grease containing a zinc salt of a dialkyl dithiophosphate |
-
1965
- 1965-02-24 GB GB8013/65A patent/GB1089463A/en not_active Expired
-
1966
- 1966-01-22 DE DE1966E0030908 patent/DE1594427A1/en active Granted
- 1966-02-16 US US527754A patent/US3493507A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US3493507A (en) | 1970-02-03 |
GB1089463A (en) | 1967-11-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
C3 | Grant after two publication steps (3rd publication) | ||
E77 | Valid patent as to the heymanns-index 1977 | ||
EF | Willingness to grant licences |