DE944678C - Lubricating oils - Google Patents

Lubricating oils

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Publication number
DE944678C
DE944678C DEB31566A DEB0031566A DE944678C DE 944678 C DE944678 C DE 944678C DE B31566 A DEB31566 A DE B31566A DE B0031566 A DEB0031566 A DE B0031566A DE 944678 C DE944678 C DE 944678C
Authority
DE
Germany
Prior art keywords
oil
lubricating oils
acids
soluble
acid
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
Application number
DEB31566A
Other languages
German (de)
Inventor
Dr Fritz Christmann
Dr Hans Engel
Dr Walter Simon
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DEB14845A external-priority patent/DE865339C/en
Application filed by BASF SE filed Critical BASF SE
Priority to DEB31566A priority Critical patent/DE944678C/en
Application granted granted Critical
Publication of DE944678C publication Critical patent/DE944678C/en
Expired legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix 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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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix 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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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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    • C10M2207/16Naphthenic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/20Rosin acids
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/044Acids; Salts or esters thereof
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    • C10M2211/06Perfluorinated compounds
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2215/26Amines
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    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/046Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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    • C10M2217/06Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
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    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
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    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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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

Gegenstand des Patentes 865 339 sind Schmieröle, die durch einem Gehalt an öllöslichen Zinksalzen von Carbonsäuren mit mindestens 5 Kohlenstoffatomen im Molekül und an öllöslichen Umsetzungsprodukten von Phosphorpentasulfid mit organischen Hydroxylverbindungen gekennzeichnet sind.The subject of patent 865 339 are lubricating oils that contain oil-soluble zinc salts of carboxylic acids with at least 5 carbon atoms in the molecule and of oil-soluble reaction products of phosphorus pentasulphide with organic ones Hydroxyl compounds are labeled.

Gegenstand des Patentes 934 184 sind Schmieröle, die an Stelle der öllöslichen Zinksalze von Carbonsäuren mit mindestens 5 Kohlenstoffatomen im Molekül öllösliche Erdalkalisake schwefelhaltiger Carbonsäuren mit mindestens 5, zweckmäßig 10 oder mehr Kohlenstoffatomen im Molekül enthalten.The subject of patent 934 184 are lubricating oils that replace the oil-soluble zinc salts of Carboxylic acids with at least 5 carbon atoms in the molecule, oil-soluble alkaline earth salts containing sulfur Carboxylic acids with at least 5, suitably 10 or more carbon atoms in the molecule contain.

Gegenstand des Patentes 934 185 sind Schmieröle, die an Stelle der öllöslichen Zinksalze von Carbonsäuren mit mindestens 5 Kohlenstoffatomen im Molekül Ester von schwefelhaltigen Carbonsäuren mit mindestens 5, zweckmäßig 10 oder mehr Kohlenstoffatomen im Molekül enthalten.The subject of the patent 934 185 are lubricating oils that replace the oil-soluble zinc salts of Carboxylic acids with at least 5 carbon atoms in the molecule Esters of sulfur-containing carboxylic acids contain at least 5, suitably 10 or more carbon atoms in the molecule.

Gegenstand des Patentes 941^687 sind Schmieröle, die an Stelle der öllöslichen Umsetzungsprödukte von Phosphorpentasulfid mit organischen Hydroxylverbindungen öllösliche Umsetzungsprodukte von Phosphorpentasulfid mit flüssigen oder festen aliphatischen Kohlenwasserstoffen oder Terpenkohlenwasserstoffen enthalten.The subject of patent 941 ^ 687 are lubricating oils, instead of the oil-soluble conversion products of phosphorus pentasulphide with organic ones Hydroxyl compounds Oil-soluble reaction products of phosphorus pentasulphide with liquid ones or solid aliphatic hydrocarbons or terpene hydrocarbons.

Es wurde gefunden, daß Schmieröle nach Patent 865 339 sowie den Patenten 934 184, 934 185 und 941 687, die als weiteren Bestandteil die an sich als Schmierölzusätze bekannten Alkylphenol-It has been found that lubricating oils according to patent 865 339 and patents 934 184, 934 185 and 941 687, which contain the alkylphenol, known per se as lubricating oil additives, as a further component

sulfide oder derenEster und bzw. oder Sulfonsäuren enthalten, die Bildung kohlenstoffhaltiger Ablagerungen auf den Kolben des Motors in besonders hohem Maße verhindern.sulfides or their esters and / or sulfonic acids, the formation of carbonaceous deposits on the piston of the engine to a particularly high degree.

Als Alkylphenolsulfide kommen Mono- oder Disulfide in Betracht, in denen die Schwefelbrücke gleiche oder verschiedene Alkylphenolreste verbindet, z. B. Kresol-, Xylenol-, Isobutylphenol-, Isoamylphenol·, Hexylphenol-, Heptylphenoli-, Octylphenol-, Dodecylphenol- und Octodecylphenolreste. Auch Phenole, die mit chlorierten Erdölfraktionen oder chloriertem Paraffin oder mit entsprechenden Olefinen alkyliert worden sind, oder 'solche, die die Alkylreste verzweigter Alkohole aus der Isobutyl-. alkoholsynthese enthalten, können als Grundstoff für die Alkylphenolsulfide dienen. Diese können noch weitere Sufestittfenten enthalten, z. B. Carboxylgruppen, funktionell veränderte halogenfreie Carboxylgruppen, wie Ester- oder Amidgruppen, ao sowie Ätherreste enthaltende Substituenten. Die Alkylphenolsulfide können ganz oder teilweise mit ein- oder mehrbasischen Säuren verestert werden. Man verwendet hierbei z. B. natürliche Fettsäuren, wie Palmitinsäure oder Stearinsäure, ferner die Fettsäuren, die bei der Oxydation von Paraffin und ähnlichen Kohlenwasserstoffen in der flüssigen Phase entstehen. Auch sind diejenigen Säuren brauchbar,, die man durch Oxydation der bei der Umsetzung von Oxyden des Kohlenstoffs mit Wasserstoff gebildeten höheren Alkohole erhält, ferner die Säuren, die durch Einwirkung von Kohlenoxyd' und Wasser auf Olefing entstehen, und-"? ferner auch mehrbasisch« Säuren, wie Oxalsäure, Bernsteinsäure, Glutarsäure, Adipinsäure und Korksäure. Mit Vorteil wird die Veresterung derart durchgeführt, daß noch freie Hydroxylgruppen mwerestert bleiben, um in diese Ester noch Metalle, die oben genannt sind, einführen zu können. Als .Sulfonsasien eignen sich öllösliche Erdölsulfonsäuren, zweckmäßig cyclische Sulfonsäuren.Suitable alkylphenol sulfides are mono- or disulfides in which the sulfur bridge connecting identical or different alkylphenol radicals, e.g. B. cresol, xylenol, isobutylphenol, Isoamylphenol, hexylphenol, heptylphenol, octylphenol, Dodecylphenol and octodecylphenol residues. Also phenols made with chlorinated petroleum fractions or chlorinated paraffin or have been alkylated with corresponding olefins, or 'those which the Alkyl radicals of branched alcohols from the isobutyl. Containing alcohol synthesis can be used as a raw material serve for the alkylphenol sulfides. These can also contain other Sufestittenten, z. B. carboxyl groups, functionally modified halogen-free carboxyl groups, such as ester or amide groups, ao as well as substituents containing ether residues. The alkylphenol sulfides can be wholly or partially with monobasic or polybasic acids are esterified. One uses here z. B. natural fatty acids, like palmitic acid or stearic acid, furthermore the fatty acids which are involved in the oxidation of paraffin and similar hydrocarbons arise in the liquid phase. Also those are acids useful, which one can use by oxidation of the reaction of oxides of carbon with Hydrogen formed higher alcohols, also the acids obtained by the action of Carbon monoxide and water are formed on olefins, and- "? also polybasic acids such as oxalic acid, succinic acid, glutaric acid, adipic acid and Suberic acid. The esterification is advantageously carried out in such a way that there are still free hydroxyl groups mwerestert to stay in these esters yet Metals, which are mentioned above, to be able to import. Oil-soluble petroleum sulfonic acids are suitable as sulfonic acids, expediently cyclic sulfonic acids.

mit einer oder mehreren Alkylgruppen, die 6 bis 15 Köhlenstoffatome in der Alkylgruppe enthalten, insbesondere ihre Salze.with one or more alkyl groups containing 6 to 15 carbon atoms in the alkyl group, especially their salts.

• Die Mischung der Komponenten wird in der Weise vorgenommen, daß man etwa 40 bis 70% -öllösliche Erdalkalisalze schwefelhaltiger Carbonsäuren oder deren Ester, 10 bis 20 % der Umsetzungsprodukte von Phosphorsulfiden mit Kohlenwasserstoffen und 10 bis 40% Alkylphenolsulfid verwendet. Dieses Gemisch wird einem Schmieröl in einer Menge von 0,1 bis 10 % zugegeben. Gleichzeitig kann man noch Schaumverhinderungsmittel, Stockpunktserniedriger und Viskositätsverbesserer zusetzen.• The components are mixed in such a way that about 40 to 70% - Oil-soluble alkaline earth salts of sulfur-containing carboxylic acids or their esters, 10 to 20% of the reaction products of phosphorus sulfides with hydrocarbons and 10 to 40% alkylphenol sulfide used. This mixture is added to a lubricating oil in an amount of 0.1 to 10%. Simultaneously Antifoaming agents, pour point depressants and viscosity improvers can also be used to add.

Beispielexample

130 Teile Propylester einer Spermölfettsäure, die mit gemahlenem Schwefel bei etwa 2000 behandelt und mit Bleicherde raffiniert wurde, 60 Teile der Bariumverbindung von Heptylphenolsulfid und 60 Teile eines öllöslichen Zink-Calcium-Salzes einer Dodecylbenzolsulfonsäure werden in 670 Teilen Motorenöl bei ioo° gelöst. Dann gibt man 180 Teile eines Bariumsalzes aus einem Umsetzungsprodukt von Terpentinöl mit Phosphorperitasulfid zu, das bei 50 bis 1300 hergestellt wurde. Dieses Produkt wird mit geringen Mengen gebranntem Kalk, Wasser und Methanol bei 80 bis 1300 behandelt und dabei leicht alkalisch gemacht.130 parts of propyl ester of a sperm oil, which was treated with ground sulfur at approximately 200 0 refined with bleaching earth, 60 parts of the barium compound of Heptylphenolsulfid and 60 parts of an oil-soluble zinc-calcium salt of dodecylbenzenesulfonic acid are dissolved in 670 parts of motor oil at ioo °. Are then added to 180 parts of a barium salt of a reaction product of turpentine with Phosphorperitasulfid prepared at 50 to 130 0th This product is treated with small amounts of quick lime, water and methanol at 80 to 130 0 thereby made slightly alkaline.

Nach dem Zentrifugieren erhält man ein Schmieröltverbesserungsmittel mit ausgezeichneten Detergent- und Inhibitoreigenschaften.A lubricating oil improver is obtained after centrifugation with excellent detergent and inhibitor properties.

Claims (1)

PATENTANSPRUCH:PATENT CLAIM: Schmieröle nach Patent 865 339 sowie nach den Patenten 934184, 934 185 und 941 687, dadurch gekennzeichnet, daß die Schmieröle als weiteren Bestandteil Alkylphenolsulfide oder deren Ester und bzw. oder Sulfonsäuren enthalten. v Lubricating oils according to patent 865 339 and according to patents 934184, 934 185 and 941 687, characterized in that the lubricating oils contain alkylphenol sulfides or their esters and / or sulfonic acids as a further component. v 609534 6.56609534 6.56
DEB31566A 1951-05-03 1954-06-26 Lubricating oils Expired DE944678C (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1107867B (en) * 1959-02-06 1961-05-31 Exxon Research Engineering Co Mineral lubricating oil
DE2436564A1 (en) * 1973-09-07 1975-04-24 Exxon Research Engineering Co LUBRICATING OIL CONDITIONS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1107867B (en) * 1959-02-06 1961-05-31 Exxon Research Engineering Co Mineral lubricating oil
DE2436564A1 (en) * 1973-09-07 1975-04-24 Exxon Research Engineering Co LUBRICATING OIL CONDITIONS

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