WO2017050982A1 - Lubricant compositions - Google Patents

Lubricant compositions Download PDF

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Publication number
WO2017050982A1
WO2017050982A1 PCT/EP2016/072719 EP2016072719W WO2017050982A1 WO 2017050982 A1 WO2017050982 A1 WO 2017050982A1 EP 2016072719 W EP2016072719 W EP 2016072719W WO 2017050982 A1 WO2017050982 A1 WO 2017050982A1
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WO
WIPO (PCT)
Prior art keywords
oil
alkyl
composition according
acid
esters
Prior art date
Application number
PCT/EP2016/072719
Other languages
German (de)
French (fr)
Inventor
Hans-Jürgen SCHOLZ
Original Assignee
Addinol Lube Oil Gmbh
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
Application filed by Addinol Lube Oil Gmbh filed Critical Addinol Lube Oil Gmbh
Priority to CN201680056512.7A priority Critical patent/CN108138073A/en
Priority to EP16770284.4A priority patent/EP3353271B1/en
Priority to US15/761,763 priority patent/US20190085259A1/en
Publication of WO2017050982A1 publication Critical patent/WO2017050982A1/en

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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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • C10M169/044Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
    • 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
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/36Esters of polycarboxylic acids
    • 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
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • 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
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/48Lubricating compositions characterised by the base-material being a macromolecular compound containing phosphorus
    • 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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/04Hydroxy compounds
    • C10M129/10Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
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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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/66Epoxidised acids or esters
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/68Esters
    • C10M129/70Esters of monocarboxylic acids
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/12Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/38Heterocyclic nitrogen compounds
    • C10M133/44Five-membered ring containing nitrogen and carbon only
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
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    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/10Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
    • C10M145/12Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate monocarboxylic
    • C10M145/14Acrylate; Methacrylate
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
    • C10M2203/1025Aliphatic fractions used as base material
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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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
    • C10M2207/24Epoxidised acids; Ester derivatives thereof
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/08Halogenated waxes
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/042Sulfate esters
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/043Ammonium or amine salts thereof
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/047Thioderivatives not containing metallic elements
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/049Phosphite
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/06Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/02Viscosity; Viscosity index
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10Inhibition of oxidation, e.g. anti-oxidants
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/18Anti-foaming property
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/66Hydrolytic stability
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants

Definitions

  • the present invention relates to lubricant compositions which are particularly suitable for the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products.
  • Lubricating oils for turbines and compressors are known from the prior art.
  • WO 201 1/070141 describes a lubricating oil composition which contains, in addition to a base oil, a succinic acid derivative and an epoxy compound as additives.
  • WO 2008/074760 also describes lubricating oil compositions known as
  • Additives contain an aspartic acid derivative and an epoxy compound or a fatty acid ester of a polyhydric alcohol.
  • Lubricants for turbocompressors or turbines which serve for the compression of chlorine or chlorine-containing products, are known. These lubricants usually comprise a highly refined base oil mixture, an additive combination for rust and oxidation inhibition and optionally defoamers.
  • EP extreme pressure / high pressure
  • lubricants from the prior art have the disadvantage of low resistance to chlorine or chlorine-containing products and cause corrosion of metals that come into contact with the chlorine-containing lubricants.
  • the lubricants of the prior art have a resistance to chlorine of up to at most 50 ppm in the oil. However, this is insufficient because chlorine dissolves in significantly higher quantities in lubricating oils.
  • the present invention is therefore based on the object to provide a lubricant composition which has improved resistance to chlorine and chlorine-containing products and should not cause corrosion.
  • a lubricant composition comprising a base oil, a hydrolysis protection component and a rust and oxidation inhibitor.
  • the present invention therefore relates to lubricant compositions comprising a) a base oil having a viscosity of 30 to 70 mm 2 / s at 40 ° C, b) a hydrolysis protective component comprising at least one C 2 -C 22 -fatty acid C 1 -C 12 -alkyl ester and / or epoxidized at least one epoxidized C 11 -C 22 fatty acid glyceride, having an epoxide oxygen content of 1 to 10 wt .-%, based on the total mass of epoxidized fatty acid Ci-Ci2-alkyl ester and / or epoxidized fatty acid glyceride, and c) a rust and oxidation inhibitor selected under at least one single or multiple Ci-Ci2-alkyl-substituted phenol, at least one aryl amine and at least one mono- or polysubstituted triazole and mixtures of two or more of these components.
  • the viscosity of the hydrocracking oil is to be understood as meaning the kinematic viscosity, which is determined with a Stabinger Viscometer SVM 3000, Anton Paar GmbH, at 40 ° C.
  • Epoxy oxygen content means the percentage by weight of oxygen, based on the total mass of epoxidized compounds.
  • the composition according to the invention comprises, as component a), a base oil with a viscosity index of> 120, in particular 130 130, the viscosity being measured at a temperature of 40 ° C. and 100 ° C. with a Stabinger Viscometer SVM 3000, Anton Paar GmbH ,
  • the base oil comprises at least one oil of quality group III of the base oils according to the classification of the American Petroleum Institute.
  • Group III base oils are mineral oils which have undergone strong hydrocracking and further dewaxing. These oils are characterized by very good oxidation stability and generally have a viscosity index of more than 120.
  • component a) is thus a base oil comprising at least one hydraulic oil.
  • the base oil of component a) has a viscosity of 40 to 60 mm 2 / s at 40 ° C.
  • the base oil is generally contained in the composition in an amount of at least 80% by weight, preferably at least 90% by weight and in particular at least 95% by weight, based in each case on the total weight of the composition.
  • component a) additionally comprises at least one further base oil component selected from mineral oils, natural oils, hydrogenated polyolefins, poly- ⁇ -olefins of olefins having 8 to 14 carbon atoms, for example poly-1 -decene or oligomers of different olefins with 8 to 14 carbon atoms, polyisobutenes having a molecular weight of 300 to 6000 g / mol, esters of aliphatic dicarboxylic acids such as azelaic acid, sebacic acid or adipic acid, with a polyglycol having a molecular weight of 500 to 2500 g / mol and a primary C6-Ci8 alcohol or Esters of aliphatic dicarboxylic acids, such as azelaic acid, sebacic acid or adipic acid, with a polyglycol having a molecular weight of 500 to 2500 g / mol and a monocarboxylic acid
  • the amount of another base oil component is in the range of 1 to 20 weight percent, based on the total amount of Grundol component (a).
  • the lubricant composition according to the invention comprises as component b) a hydrolysis protection component.
  • the antihydrolysis component is generally contained in the composition in an amount of 0.05 to 1.5% by weight, preferably 0.05 to 0.9% by weight, based in each case on the total weight of the composition.
  • the fatty acid of the fatty acid alkyl esters and fatty acid glycerides of component b) is selected from fatty acids containing natural oils such as soybean oil, thistle oil, grape seed oil, mustard oil, coriander oil, linseed oil, rapeseed oil, borage oil, tung oil, evening primrose oil, walnut oil, Hemp oil, sunflower oil, olive oil, palm oil, peanut oil, coconut oil, castor oil or fish oil are based, preferably among the fatty acids, which are based on soybean oil, linseed oil, rapeseed oil or fish oil.
  • natural oils such as soybean oil, thistle oil, grape seed oil, mustard oil, coriander oil, linseed oil, rapeseed oil, borage oil, tung oil, evening primrose oil, walnut oil, Hemp oil, sunflower oil, olive oil, palm oil, peanut oil, coconut oil, castor oil or fish oil are based, preferably among the fatty acids, which are based on soybean oil,
  • fatty acids which may be based on the abovementioned oils are unsaturated fatty acids having 1 to 22 carbon atoms, for example undecylenic acid, myristoleic acid, palmitoleic acid, petroselinic acid, oleic acid, elaidic acid, vaccenic acid, gadoleic acid, losenoic acid, cetoleic acid, erucic acid, Linoleic acid, alpha-linolenic acid, gamma-linolenic acid, calendic acid, punicic acid, alpha
  • C 1 -C 12 -alkyl esters of the epoxidized fatty acids are the C 6 -C 10 -alkyl esters, in particular the C 8 -alkyl esters, e.g. the 2-ethylhexyl esters, preferred.
  • C1-C12-alkyl are meant linear or branched saturated hydrocarbon radicals having 1 to 12 carbon atoms.
  • component b) comprises mixtures of epoxidized Cn-C22-fatty acid-Ci-Ci2-alkyl esters and epoxidized Cn-C22-Fettklareglyceriden.
  • the fatty acid alkyl esters may be present as a fatty acid alkyl ester or as a mixture of two or more fatty acid alkyl esters.
  • the fatty acid glycerides may be present as a fatty acid glyceride or as a mixture of two or more fatty acid glycerides.
  • the percentage by weight of oxygen, based on the total mass of epoxidized fatty acid C 1 -C 12 -alkyl ester and / or epoxidized fatty acid glyceride, in one embodiment of the lubricant composition according to the invention is 3 to 8% by weight.
  • the production of the Cn-C22-fatty acid-Ci-Ci2-alkylester and epoxidized C11-C22-Fettklareglyceride is carried out in the usual manner, for example according to the in J. Am. Chem. Soc. 62 (1945), pp. 412-414.
  • the determination of the epoxide content is carried out in a customary manner, for example according to the method described in EP 1693359 or DIN 16945.
  • the lubricant composition of the invention comprises as component c) a rust and / or oxidation inhibitor.
  • the rust and / or oxidation inhibitor is generally contained in the composition in an amount of 0.05 to 2% by weight, preferably 0.05 to 1.0% by weight, based in each case on the total weight of the composition.
  • component (c) comprises at least one mono- or polysubstituted C1-C12-alkyl-substituted phenol or at least one arylamine or at least one singly or multiply substituted triazole. In a further embodiment of the invention, component (c) comprises at least one singly or multiply C 1 -C 12 -alkyl-substituted phenol and at least one arylamine or at least one singly or multiply substituted triazole. In a further embodiment of the invention, component (c) comprises at least one arylamine and at least one singly or multiply substituted triazole.
  • component (c) comprises at least one singly or multiply C 1 -C 12 -alkyl-substituted phenol and at least one arylamine and at least one singly or multiply substituted triazole.
  • the Ci-Ci2-alkyl-substituted phenol of the component c) is selected from Ci-Ci2-alkyl-substituted phenols with sterically demanding substituents, such as isopropyl or tert. Butyl.
  • the phenol can be substituted with one substituent or with 2, 3, 4 or 5 substituents.
  • the phenol is substituted twice or three times.
  • the Ci-Ci2-alkyl-substituted phenols are selected from 2,6-di-tert-butylphenol, 4-methyl-2,6-di-tert-butylphenol, 2,4,6-tri-tert-butylphenol , 2-tert-butylphenol, 2,6-diisopropylphenol, 2-methyl-6-tert-butylphenol, 2,4-dimethyl-6-tert-butylphenol and 4-ethyl-2,6-di-tert-butylphenol.
  • Component c) may comprise a C 1 -C 12 -alkyl-substituted phenol or a mixture of two or more C 1 -C 12 -alkyl-substituted phenols.
  • component c) comprises at least one arylamine which is selected from
  • R 1 , R 2 , R 3 and R 4 are identical or different and represent hydrogen or C 1 -C 6 -alkyl
  • R 5 is hydrogen or Ci-Cis-alkyl
  • R 6 is hydrogen or Ci-Cis-alkyl.
  • R 1 , R 2 , R 3 and R 4 may each stand for hydrogen.
  • at least one of the radicals is an alkyl group having 1 to 18 carbon atoms, especially 8 to 18 carbon atoms.
  • the alkyl groups may be linear or branched.
  • Such an alkyl group may include a methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, amyl group, hexyl group, heptyl group, octyl group, 2-ethylhexyl group, nonyl group, isononyl group , Decyl, undecyl, dodecyl, tridecyl, isotridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, or octadecyl.
  • R 5 is a hydrogen atom or an alkyl group having 1 to 18 carbon atoms.
  • R 5 is an alkyl group of 1 to 18 carbon atoms, more preferably 8 to 18 carbon atoms.
  • the alkyl group having 1 to 18 carbon atoms is as defined for R 1 to R 4 .
  • R 6 is a hydrogen atom or an alkyl group having 1 to 18 carbon atoms.
  • R 6 is an alkyl group of 1 to 18 carbon atoms, more preferably 8 to 18 carbon atoms.
  • the alkyl group having 1 to 18 carbon atoms is as defined for R 1 to R 4 .
  • Component c) may comprise an alkyldiphenylamine of the general formula (I) alone, but also mixtures of two or more alkyldiphenylamines of the general formula (I). Furthermore, component c) may comprise a phenyl-alphanaphthylamine of general formula (II) alone, or else mixtures of two or more phenyl-alpha-naphthylamines (II). Furthermore, component c) may comprise a phenyl-beta-naphthylamine of the general formula (III) alone, or else mixtures of two or more phenyl-alpha-naphthylamines (III). com- Component c) may additionally comprise mixtures of two or more of the arylamines (I), (II) and (III).
  • mixtures of at least two different arylamines are part of component c).
  • Component c) may comprise a mono- or polysubstituted triazole.
  • the substituted triazole is selected from alkyl- and / or aryl-substituted triazoles, preferably Ci-Ci2-alkyl and / or C6-Ci8-aryl-substituted 1, 2,3-triazoles and 1, 2,4- triazoles.
  • Ci-Ci2-alkyl are linear, branched or cyclic alkyl radicals having 1 to 12 carbon atoms to understand.
  • C 6 -C 18 aryl are aromatic radicals having 6 to 18 carbon atoms, e.g. mononuclear aromatic radicals or two or more nuclear aromatic radicals which may be fused or bridged by a chemical compound or a Ci- C6-alkyl bridge to understand.
  • Examples of monosubstituted 1,2,4-triazoles are 1-alkyl or aryl-substituted-1H-1, 2,4-triazoles, 3-alkyl or aryl-substituted-1H-triazoles or 4-alkyl or aryl substituted-4H-1, 2,4-triazoles.
  • di-substituted 1,2,4-triazoles are 1,3-alkyl and / or aryl-disubstituted-1H-1, 2,4-triazoles, 1,5-alkyl and / or aryl-disubstituted-1H- 1, 2,4-triazoles, 3,4-alkyl and / or aryl-disubstituted-4H-1, 2,4-triazoles or 3,5-alkyl and / or aryl-disubstituted-s-triazoles.
  • triply substituted 1,2,4-triazoles are 1,3,5-alkyl and / or aryl-trisubstituted-1H-1, 2,4-triazoles or 3,4,5-alkyl and / or aryl-trisubstituted -4H-1, 2,4-triazoles.
  • Examples of monosubstituted 1,2,3-triazoles are 1-alkyl or aryl-substituted-1H-1,2,3-triazoles or 2-alkyl or aryl-substituted-2H-1,2,3-triazoles.
  • Examples of di-substituted 1,2,3-triazoles are 1,4-alkyl and / or aryl-disubstituted-1H-1,2,3-triazoles or 2,4-alkyl and / or aryl-disubstituted-2H -1,2,3-triazoles.
  • triply substituted 1,2,3-triazoles are 1, 4,5-alkyl and / or aryl-trisubstituted-2H-1,2,3-triazoles or 2,4,5-alkyl and / or aryl-trisubstituted 1 H-1,2,3-triazoles.
  • Suitable representatives of component c) are commercially available.
  • the composition according to the invention additionally comprises a defoamer.
  • the antifoam may be used, for example, in an amount of 0.001 to 0.1% by weight, preferably 0.005 to 0.05% by weight, based on the total composition of the composition according to the invention, be included in the composition.
  • Suitable defoamers which are suitable as an additive to the composition of the invention are homopolymers of (meth) -Ci-Ci8-alkyl acrylates, copolymers of at least two (meth) -Ci-Ci8-alkyl acrylates or mixtures thereof in question.
  • the defoamers used are homopolymers of (meth) -Ci-Cs-alkyl acrylates, copolymers of at least two (meth) -Ci-C8-alkyl acrylates or mixtures thereof.
  • Alkyl stands for linear or branched alkyl groups, such as methyl, ethyl, propyl, n-butyl, isobutyl, pentyl, hexyl, 2-ethylhexyl, heptyl or octyl groups. Preference is given to the methyl, ethyl, n-butyl and 2-ethylhexyl groups.
  • the polymers may also contain other monomers incorporated, such as (meth) acrylic acid, (meth) acrylamide, hydroxy-C 2 -C 6 -alkyl (meth) acrylate.
  • copolymers of at least two (meth) -Ci-C8-alkyl acrylates are used as antifoams.
  • An example of such defoamers are copolymers of n-butyl acrylate and / or 2-ethylhexyl acrylate and methyl acrylate and / or ethyl acrylate.
  • the defoamer is substantially free of silicone. Substantially silicone-free means that, based on the total mass of the defoamer, less than 1% by weight, preferably 0% by weight, of silicones is contained in the defoamer. Suitable defoamers are commercially available.
  • the composition according to the invention additionally comprises an extreme pressure agent.
  • the high pressure additive can be contained in the composition, for example, in an amount of 0.001 to 0.1 wt .-%, preferably 0.002 to 0.03 wt .-%, based on the total mass of the composition according to the invention.
  • High pressure additives useful as an additive to the composition of the present invention are generally oil soluble. Suitable high-pressure additives are selected, for example, from oil-soluble organic esters of phosphoric acid, oil-soluble organic esters of phosphinic acid, oil-soluble organic esters of phosphonic acid, oil-soluble organic esters of sulfuric acid, oil-soluble organic esters of sulfurous acid, oil-soluble organic esters of sulfonic acid, amine salts of hydroxy -substituted phosphetanes, amine salts of hydroxy-substituted Thiophosphetanen, amine salts of partial esters of phosphorous acid and amine salts of partial esters of thiophosphorigenic acid.
  • Phosphoric acid, phosphinic acid, phosphonic acid, sulfuric acid, sulfurous acid and sulfonic acid are, for example, with alcohols with e.g. 4 to 18 carbon atoms esterified.
  • Examples of amine salts of hydroxy-substituted phosphetanes, hydroxy-substituted thiophosphetanes, partial esters of phosphorous acid and partial esters of thiophosphorous acid are the C 6 -C 12 -alkylamine salts thereof, preferably the octylamine salts thereof.
  • Partial esters of phosphorous acid and thiophosphorous acid are not completely esterified at all OH groups of the underlying free acids.
  • the partial esterification of the phosphorous acid and the thiophosphorous acid can be carried out, for example, with alcohols with e.g. 4 to 18 carbon atoms take place.
  • the composition of the invention comprises a high pressure additive selected from alkyl thiophosphate esters.
  • alkyl thiophosphate esters are C 1 -C 6 -alkyl esters of thiophosphoric acid.
  • the alkylthiophosphoric acid esters may have three identical alkyl radicals, two or three different from one another. Suitable high pressure additives are commercially available.
  • the lubricant composition of the invention comprises a high pressure additive or a mixture of two or more high pressure additives different from each other.
  • the lubricant composition comprises at least one defoamer and at least one high pressure additive, wherein the defoamer and the high pressure additive are as defined above.
  • the lubricant composition according to the invention comprises a) the base oil having a viscosity of 30 to 70 mm 2 / s at 40 ° C., in particular a hydrocracker oil having a viscosity of 40 to 50 mm 2 / s at 40 ° C., b) 0.05 to 1, 5 wt .-%, in particular 0.05 to 0.9 wt .-%, of the hydrolysis protection component, c) 0.05 to 2 wt .-%, in particular 0.05 to 1, 0 D) optionally from 0.001 to 0.1% by weight, in particular from 0.005 to 0.05% by weight, of an antifoam, and e) optionally from 0.001 to 0.1% by weight of the rust and oxidation inhibitor; .-%
  • the lubricant compositions according to the invention contain no succinic acid ester and / or no aspartic acid derivative, in particular no aspartic acid acylated on the nitrogen atom or an ester thereof.
  • the succinic esters correspond to the formula
  • Xi and X2 independently of one another are H or alkyl, alkenyl or hydroxyalkyl having 3 to 6 carbon atoms and X3 has 1 to 30 carbon atoms and is alkyl, alkenyl, alkyl having ether bonds or hydroxyalkyl,
  • Xi and X2 are H, alkyl or hydroxyalkyl having 3 to 6 carbon atoms
  • X3 is alkyl having 1 to 30 carbon atoms
  • X 4 for saturated or unsaturated carboxylic acid groups having radicals, in particular alkyl or alkenyl radicals, with 1 to 30 carbon atoms, alkenyl or hydroxyalkyl.
  • the lubricant compositions according to the invention have the advantage of high resistance to chlorine or chlorine-containing products.
  • the lubricant compositions according to the invention are resistant to chlorine contents of more than 50 ppm up to 2000 ppm.
  • the lubricant compositions according to the invention for the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products are suitable.
  • the invention further relates to the use of the lubricant compositions according to the invention for the lubrication of turbines or (turbo) compressors.
  • lubricant compositions according to the invention are particularly suitable for use in the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products.
  • the lubricant compositions of the invention are prepared, for example, by mixing (using a suitable stirrer) the above components in a suitable device, e.g. a mixing kettle, received.
  • a suitable device e.g. a mixing kettle
  • Applying the compositions to the parts to be lubricated e.g. Feedthroughs for strokes of a turbine or a (turbo) compressor can be done, for example, by spraying and / or spreading of the compositions on said parts.
  • a suitable device e.g. a mixing kettle
  • Applying the compositions to the parts to be lubricated e.g. Feedthroughs for strokes of a turbine or a (turbo) compressor can be done, for example, by spraying and / or spreading of the compositions on said parts.
  • the following examples serve to illustrate the invention without limiting it.
  • Example 1 The following components were charged in the proportions indicated in a mixing vessel and mixed therein to form a lubricant composition. a) 87.5% by weight, based on the total mass of the composition, of a hydraulic oil with a viscosity of 40 to 55 mm 2 / s at 40 ° C .; b) 1 1, 6 wt .-% of a formulation, based on the total mass of the composition containing about 4 wt .-% of at least one epoxidized C11-C22- Fatty acid C 1 -C 12 -alkyl ester based on rapeseed oil with a total oxygen content of about 7% by weight (remainder rapeseed oil); c) 0.8% by weight, based on the total weight of the composition, of a formulation containing about 15% by weight of 2-tert-butylphenol and phenyl-a-naphthylamine
  • Weight ratio 2 1 contains (balance oil); and d) 0, 1 wt .-%, based on the total weight of the composition, of at least one polymeric defoamer (balance oil).
  • a standard method for the determination of corrosion according to DI N ISO 7120 was modified in the lubricant industry. Instead of water and oil, a 2000 ppm chlorine offset lubricant composition according to Example 1 was presented as a test liquid and the test specimens used for 24 hours at 60 ° C with stirring (1000 rev / min) left.
  • the specimens used were both the specimens described in DIN ISO 7120 made of steel, and of white metal, which is usually used as a bearing metal in compressors. After 24 hours, the stirring was stopped and the test pieces were taken out of the test liquid. After draining, the test piece was rinsed with cleaning solution and the degree of corrosion was assessed according to the DI N ISO 7120 classification. A specimen is considered rusted if any rust or rust streak is visible. Are both specimens stainless, the
  • Lubricant composition passed the test.
  • Light rust Not more than 6 rust spots of 1 mm diameter or less.
  • Moderate rust More rust than light rust, but less than 5% of rust
  • Strong rust The rust covers more than 5% of the surface of the specimens.

Abstract

The invention relates to lubricant compositions suitable in particular for lubricating turbines or (turbo) compressors used for compressing chlorine and/or products containing chlorine. The lubricant composition comprises a base oil, an anti-hydrolysis component, and a rust and oxidation inhibitor.

Description

Schmierstoffzusammensetzungen  lubricant compositions
Die vorliegende Erfindung betrifft Schmierstoffzusammensetzungen, die insbesondere für die Schmierung von Turbinen oder (Turbo)kompressoren, die zur Verdichtung von Chlor und/oder chlorhaltigen Produkten dienen, geeignet sind. The present invention relates to lubricant compositions which are particularly suitable for the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products.
Aus dem Stand der Technik sind Schmieröle für Turbinen und Kompressoren bekannt. So beschreibt die WO 201 1/070141 eine Schmierölzusammensetzung, die neben einem Grundöl ein Bernsteinsäurederivat und eine Epoxyverbindung als Additive enthält. Die WO 2008/074760 beschreibt ebenfalls Schmierölzusammensetzungen, die alsLubricating oils for turbines and compressors are known from the prior art. Thus, WO 201 1/070141 describes a lubricating oil composition which contains, in addition to a base oil, a succinic acid derivative and an epoxy compound as additives. WO 2008/074760 also describes lubricating oil compositions known as
Additive ein Asparaginsäurederivat und eine Epoxyverbindung oder einen Fettsäureester eines Polyalkohols enthalten. Auch Schmierstoffe für Turbokompressoren oder Turbinen, die zur Verdichtung von Chlor bzw. chlorhaltigen Produkten dienen, sind bekannt. Diese Schmierstoffe umfassen zumeist eine hochausraffinierte Basisölmi- schung, eine Additivkombination zur Rost- und Oxidationsinhibierung und gegebenenfalls Entschäumer. Für den Einsatz der Schmierstoffe in Kompressoren mit Getrieben ist der Zusatz von EP (extreme pressure/Hochdruck)-Zusätzen bekannt, siehe W. J. Bartz, Additive für Schmierstoffe, expert-Verlag, Renningen-Malmsheim 1994. Die oben genannten Schmierstoffe aus dem Stand der Technik weisen allerdings den Nachteil einer geringen Beständigkeit gegenüber Chlor oder chlorhaltigen Produkten auf und bewirken Korrosion bei Metallen, die mit den chlorhaltigen Schmierstoffen in Kontakt kommen. Üblicherweise weisen die Schmierstoffe aus dem Stand der Technik eine Beständigkeit gegenüber Chlor von bis zu höchstens 50 ppm im Öl. Dies ist je- doch ungenügend, weil Chlor sich in wesentlich höherer Menge in Schmierölen löst. Additives contain an aspartic acid derivative and an epoxy compound or a fatty acid ester of a polyhydric alcohol. Lubricants for turbocompressors or turbines, which serve for the compression of chlorine or chlorine-containing products, are known. These lubricants usually comprise a highly refined base oil mixture, an additive combination for rust and oxidation inhibition and optionally defoamers. For the use of lubricants in compressors with gears, the addition of EP (extreme pressure / high pressure) additives is known, see WJ Bartz, additives for lubricants, expert-Verlag, Renningen-Malmsheim 1994. The above-mentioned lubricants from the prior art However, they have the disadvantage of low resistance to chlorine or chlorine-containing products and cause corrosion of metals that come into contact with the chlorine-containing lubricants. Usually, the lubricants of the prior art have a resistance to chlorine of up to at most 50 ppm in the oil. However, this is insufficient because chlorine dissolves in significantly higher quantities in lubricating oils.
Um das Austreten von hochgiftigem Chlorgas bei der Komprimierung von Chlor in Kompressoren zu verhindern, sind für die Abdichtung nach außen besondere Sicherheitsmaßnahmen erforderlich. So werden beispielsweise Durchführungen für Hubbe- wegung mit Faltenbälgen ausgerüstet und Wellendurchführungen zusätzlich mit Sperrgas abgedichtet. An die Dichtheit und Zuverlässigkeit der eingesetzten Armaturen und Vorleitantriebe werden höchste Anforderungen gestellt. In order to prevent the leakage of highly toxic chlorine gas in the compression of chlorine in compressors, special safety measures are required for the sealing to the outside. For example, bushings for lifting movement are equipped with bellows and shaft bushings are additionally sealed with sealing gas. At the tightness and reliability of the valves and Vorleitantriebe used highest demands are made.
Tritt trotz dieser beschriebenen Sicherheitsmaßnahmen Chlor in einen Schmierstoff aus dem Stand der Technik ein, wird der Schmierstoff sehr schnell oxidiert und altert dadurch innerhalb kürzester Zeit. Weiterhin wird dabei eine Versäuerung des Schmierstoffes beobachtet. Dies äußert sich in einem starken Anstieg der Säurezahl. Durch die gleichzeitig ablaufende Zerstörung der im Schmierstoff enthaltenen Korrosionsschutzadditive geht die Schutzfunktion des Schmierstoffs gegenüber metallischen Anlagenwerkstoffen verloren. Es tritt in der Folge ein korrosiver Angriff bei Lagern und anderen Anlagenteilen auf. Der ungeplante, korrosionsbedingte Ausbau von Anlagenteilen führt zu Anlagenabstellungen und Stillständen. Die Kosten für den Ausbau der beschädigten Anlagenteile, die Reinigung der Anlage und den Ersatz der beschädigten Anlagenteile sind sehr hoch. Durch die geringe Beständigkeit gegenüber Chlor oder chlorhaltigen Produkten weisen die Schmierstoffe aus dem Stand der Technik nur eine kurze Lebensdauer auf. Occurs despite these safety measures described chlorine in a lubricant from the prior art, the lubricant is oxidized very quickly and thereby aging within a very short time. Furthermore, an acidification of the lubricant is observed. This manifests itself in a sharp increase in the acid number. By the At the same time destruction of the corrosion protection additives contained in the lubricant is lost the protective function of the lubricant compared to metallic plant materials. As a result, a corrosive attack occurs on bearings and other parts of the system. The unplanned, corrosion-related dismantling of plant components leads to plant shutdowns and shutdowns. The cost of removing the damaged equipment, cleaning the equipment and replacing the damaged equipment is very high. Due to the low resistance to chlorine or chlorine-containing products, the lubricants from the prior art have only a short life.
Der vorliegenden Erfindung liegt daher die Aufgabe zugrunde, eine Schmierstoffzusammensetzung bereitzustellen, die eine verbesserte Beständigkeit gegenüber Chlor und chlorhaltigen Produkten aufweisen und keine Korrosion bewirken soll. Insbesondere ist es Aufgabe der Erfindung eine Schmierstoffzusammensetzung mit den oben ge- nannten Eigenschaften bereitzustellen, die für die Verwendung zur Schmierung von Turbinen oder (Turbo)kompressoren, die zur Verdichtung von Chlor und/oder chlorhaltigen Produkten dienen, geeignet ist. The present invention is therefore based on the object to provide a lubricant composition which has improved resistance to chlorine and chlorine-containing products and should not cause corrosion. In particular, it is an object of the invention to provide a lubricant composition having the above-mentioned properties, which is suitable for use in the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products.
Diese Aufgabe wird gelöst durch eine Schmierstoffzusammensetzung umfassend ein Grundöl, eine Hydrolyseschutzkomponente und einen Rost- und Oxidationsinhibitor. This object is achieved by a lubricant composition comprising a base oil, a hydrolysis protection component and a rust and oxidation inhibitor.
Die vorliegende Erfindung betrifft daher Schmierstoffzusammensetzungen umfassend a) ein Grundöl mit einer Viskosität von 30 bis 70 mm2/s bei 40 °C, b) eine Hydrolyseschutzkomponente, umfassend wenigstens einen epoxidierten Cn- C22-Fettsäure-Ci-Ci2-alkylester und/oder wenigstens ein epoxidiertes C11-C22- Fettsäureglycerid, mit einem Epoxidsauerstoffgehalt von 1 bis 10 Gew.-%, bezogen auf die Gesamtmasse an epoxidiertem Fettsäure-Ci-Ci2-alkylester und/oder epoxidiertem Fettsäureglycerid, und c) einen Rost- und Oxidationsinhibitor, ausgewählt unter wenigstens einem einfach oder mehrfach Ci-Ci2-Alkyl-substituierten Phenol, wenigstens einem Arylamin und wenigstens einem einfach oder mehrfach substituierten Triazol und Gemischen aus zwei oder mehreren dieser Komponenten. The present invention therefore relates to lubricant compositions comprising a) a base oil having a viscosity of 30 to 70 mm 2 / s at 40 ° C, b) a hydrolysis protective component comprising at least one C 2 -C 22 -fatty acid C 1 -C 12 -alkyl ester and / or epoxidized at least one epoxidized C 11 -C 22 fatty acid glyceride, having an epoxide oxygen content of 1 to 10 wt .-%, based on the total mass of epoxidized fatty acid Ci-Ci2-alkyl ester and / or epoxidized fatty acid glyceride, and c) a rust and oxidation inhibitor selected under at least one single or multiple Ci-Ci2-alkyl-substituted phenol, at least one aryl amine and at least one mono- or polysubstituted triazole and mixtures of two or more of these components.
Unter der Viskosität des Hydrocracköls ist die kinematische Viskosität zu verstehen, die mit einem Stabinger Viscometer SVM 3000, Anton Paar GmbH, bei 40 °C bestimmt wird. Unter Epoxidsauerstoffgehalt ist der prozentuale Gewichtsanteil an Sauerstoff, bezogen auf die Gesamtmasse an epoxidierten Verbindungen, zu verstehen. Gemäß einer Ausführungsform umfasst die erfindungsgemäße Zusammensetzung als Komponente a) ein Grundöl mit einem Viskositätsindex von >120, insbesondere ä 130, wobei die Viskosität bei einer Temperatur von 40°C und 100 °C mit einem Stabinger Viscometer SVM 3000, Anton Paar GmbH gemessen wurde. Gemäß einer weiteren Ausführungsform umfasst das Grundöl wenigstens ein Öl der Qualitätsgruppe III der Grundöle gemäß Klassifizierung des American Petroleum Institute. Unter Grundölen der Gruppe III sind Mineralöle zu verstehen, die einem starken Hydrocracking und einer weiteren Entparaffinierung unterzogen wurden. Diese Öle zeichnen sich durch sehr gute Oxidationsstabilität aus und weisen im Allgemeinen ei- nen Viskositätsindex von mehr als 120 auf. Gemäß einer weiteren Ausführungsform handelt es sich bei der Komponente a) somit um ein Grundöl, das wenigstens ein Hyd- rocracköl umfasst. The viscosity of the hydrocracking oil is to be understood as meaning the kinematic viscosity, which is determined with a Stabinger Viscometer SVM 3000, Anton Paar GmbH, at 40 ° C. Epoxy oxygen content means the percentage by weight of oxygen, based on the total mass of epoxidized compounds. According to one embodiment, the composition according to the invention comprises, as component a), a base oil with a viscosity index of> 120, in particular 130 130, the viscosity being measured at a temperature of 40 ° C. and 100 ° C. with a Stabinger Viscometer SVM 3000, Anton Paar GmbH , According to another embodiment, the base oil comprises at least one oil of quality group III of the base oils according to the classification of the American Petroleum Institute. Group III base oils are mineral oils which have undergone strong hydrocracking and further dewaxing. These oils are characterized by very good oxidation stability and generally have a viscosity index of more than 120. According to a further embodiment, component a) is thus a base oil comprising at least one hydraulic oil.
In einer weiteren Ausführungsform weist das Grundöl der Komponente a) eine Viskosi- tät von 40 bis 60 mm2/s bei 40 °C auf. In a further embodiment, the base oil of component a) has a viscosity of 40 to 60 mm 2 / s at 40 ° C.
Das Grundöl ist in der Zusammensetzung im Allgemeinen in einer Menge von mindestens 80 Gew.-%, vorzugsweise mindestens 90 Gew.-% und insbesondere mindestens 95 Gew.-% enthalten, jeweils bezogen auf das Gesamtgewicht der Zusammensetzung. The base oil is generally contained in the composition in an amount of at least 80% by weight, preferably at least 90% by weight and in particular at least 95% by weight, based in each case on the total weight of the composition.
In einer Ausführungsform umfasst die Komponente a) zusätzlich mindestens eine weitere Grundölkomponente ausgewählt unter Mineralölen, Naturölen, hydrierten Polyole- finölen, Poly-a-Olefinen von Olefinen mit 8 bis 14 Kohlenstoffatomen, zum Beispiel Poly-1 -decen oder Oligomere verschiedener Olefine mit 8 bis 14 Kohlenstoffatomen, Polyisobutenen mit einem Molekulargewicht von 300 bis 6000 g/mol, Estern von aliphatischen Dicarbonsäuren, wie Azelainsäure, Sebacinsäure oder Adipinsäure, mit einem Polyglycol mit einem Molekulargewicht von 500 bis 2500 g/mol und einem primären C6-Ci8-Alkohol oder Estern von aliphatischen Dicarbonsäuren, wie Azelainsäure, Sebacinsäure oder Adipinsäure, mit einem Polyglycol mit einem Molekulargewicht von 500 bis 2500 g/mol und einer Monocarbonsäure (Komplexester, Ullmann's Encyc- lopedia of Industrial Chemistry, Band A15, 1990, Seiten 438-440), Ce-ds-Alkylestern der phosphorigen Säure, C6-Ci8-Alkylestern der Phosphorsäure, Diestern von C6-C12- Dicarbonsäuren mit C6-C18 Alkoholen, und Polyalkyletherölen, die perhalogeniert, z.B. perfluoriert, oder teilweise halogeniert, z.B. teilweise fluoriert, sein können. Vorzugs- weise ist die weitere Grundolkomponente ausgewählt unter Mineralölen oder hydrierten Polyolefinölen. In one embodiment, component a) additionally comprises at least one further base oil component selected from mineral oils, natural oils, hydrogenated polyolefins, poly-α-olefins of olefins having 8 to 14 carbon atoms, for example poly-1 -decene or oligomers of different olefins with 8 to 14 carbon atoms, polyisobutenes having a molecular weight of 300 to 6000 g / mol, esters of aliphatic dicarboxylic acids such as azelaic acid, sebacic acid or adipic acid, with a polyglycol having a molecular weight of 500 to 2500 g / mol and a primary C6-Ci8 alcohol or Esters of aliphatic dicarboxylic acids, such as azelaic acid, sebacic acid or adipic acid, with a polyglycol having a molecular weight of 500 to 2500 g / mol and a monocarboxylic acid (complex ester, Ullmann's Encyclopedia of Industrial Chemistry, Volume A15, 1990, pages 438-440), Ce-ds-alkyl esters of phosphorous acid, C6-Ci8-alkyl esters of phosphoric acid, diesters of C6-C12 - Dicarboxylic acids with C6-C18 alcohols, and polyalkyl ether oils which may be perhalogenated, for example perfluorinated, or partially halogenated, for example partially fluorinated. preferential The other Grundol component is selected from mineral oils or hydrogenated polyolefin oils.
Wenn vorhanden, liegt die Menge an weiterer Grundolkomponente im Bereich von 1 bis 20 Gew.-%, bezogen auf die Gesamtmenge an Grundolkomponente (a). If present, the amount of another base oil component is in the range of 1 to 20 weight percent, based on the total amount of Grundol component (a).
Die erfindungsgemäße Schmierstoffzusammensetzung umfasst als Komponente b) eine Hydrolyseschutzkomponente. Die Hydrolyseschutzkomponente ist in der Zusammensetzung im Allgemeinen in einer Menge von 0,05 bis 1 ,5 Gew.-%, vorzugsweise 0,05 bis 0,9 Gew.-%, enthalten, jeweils bezogen auf das Gesamtgewicht der Zusammensetzung. The lubricant composition according to the invention comprises as component b) a hydrolysis protection component. The antihydrolysis component is generally contained in the composition in an amount of 0.05 to 1.5% by weight, preferably 0.05 to 0.9% by weight, based in each case on the total weight of the composition.
In einer Ausführungsform der Erfindung ist die Fettsäure der Fettsäurealkylester und Fettsäureglyceride der Komponente b) ausgewählt unter den Fettsäuren, welche natür- liehen Ölen, wie Sojabohnenol, Distelöl, Traubenkernöl, Senföl, Korianderöl, Leinöl, Rüböl, Borretschöl, Tungöl, Nachtkerzenöl, Walnussöl, Hanföl, Sonnenblumenöl, Olivenöl, Palmöl, Erdnussöl, Kokosnussöl, Ricinusöl oder Fischöl zugrundeliegen, vorzugsweise unter den Fettsäuren, die Sojabohnenol, Leinöl, Rüböl oder Fischöl zugrundeliegen. In one embodiment of the invention, the fatty acid of the fatty acid alkyl esters and fatty acid glycerides of component b) is selected from fatty acids containing natural oils such as soybean oil, thistle oil, grape seed oil, mustard oil, coriander oil, linseed oil, rapeseed oil, borage oil, tung oil, evening primrose oil, walnut oil, Hemp oil, sunflower oil, olive oil, palm oil, peanut oil, coconut oil, castor oil or fish oil are based, preferably among the fatty acids, which are based on soybean oil, linseed oil, rapeseed oil or fish oil.
Beispiele für Fettsäuren, die den oben genannten Ölen zugrundeliegen können, sind ungesättigte Fettsäuren mit 1 1 bis 22 Kohlenstoffatomen, zum Beispiel Undecylensäu- re, Myristoleinsäure, Palmitoleinsäure, Petroselinsäure, Ölsäure, Elaidinsäure, Vac- censäure, Gadoleinsäure, leosensäure, Cetoleinsäure, Erucasäure, Linolsäure, Alpha- Linolensäure, Gamma-Linolensäure, Calendulasäure, Punicinsäure, Alpha-Examples of fatty acids which may be based on the abovementioned oils are unsaturated fatty acids having 1 to 22 carbon atoms, for example undecylenic acid, myristoleic acid, palmitoleic acid, petroselinic acid, oleic acid, elaidic acid, vaccenic acid, gadoleic acid, losenoic acid, cetoleic acid, erucic acid, Linoleic acid, alpha-linolenic acid, gamma-linolenic acid, calendic acid, punicic acid, alpha
Elaeostearinsäure, Beta-Elaeostearinsäure, Arachidonsäure, Timnodonsäure, Cervon- säure oder Clupanodonsäure. Elaeostearic acid, beta-elaeostearic acid, arachidonic acid, timnodonic acid, cervonic acid or clupanodonic acid.
Unter den Ci-Ci2-Alkylestern der epoxidierten Fettsäuren sind die C6-Cio-Alkylester, insbesondere die Cs-Alkylester, z.B. die 2-Ethylhexylester, bevorzugt. Unter C1-C12- Alkyl sind lineare oder verzweigte gesättigte Kohlenwasserstoffreste mit 1 bis 12 Kohlenstoffatomen zu verstehen. Among the C 1 -C 12 -alkyl esters of the epoxidized fatty acids are the C 6 -C 10 -alkyl esters, in particular the C 8 -alkyl esters, e.g. the 2-ethylhexyl esters, preferred. By C1-C12-alkyl are meant linear or branched saturated hydrocarbon radicals having 1 to 12 carbon atoms.
Unter den genannten Fettsäureglyceriden sind Triester des Glycerols mit C11-C22- Fettsäuren zu verstehen. Das Glycerol kann dabei dreifach mit der jeweils identischen Fettsäure oder mit zwei oder drei voneinander verschiedenen Fettsäuren verestert sein. Die epoxidierten Cn-C22-Fettsäure-Ci-Ci2-alkylester und epoxidierten C11-C22- Fettsäureglyceride können jeweils einzeln oder gemeinsam als Mischungen als Bestandteil der Hydrolyseschutzkomponente vorliegen. Vorzugsweise umfasst die Komponente b) Mischungen von epoxidierten Cn-C22-Fettsäure-Ci-Ci2-alkylestern und epoxidierten Cn-C22-Fettsäureglyceriden. Among the fatty acid glycerides mentioned are triesters of glycerol with C11-C22 fatty acids to understand. The glycerol can be esterified in triplicate with the respectively identical fatty acid or with two or three different fatty acids. The epoxidized Cn-C22-fatty acid-Ci-Ci2-alkylester and epoxidized C11-C22-Fettsäureglyceride can each be present individually or together as mixtures as a component of the hydrolysis protection component. Preferably, component b) comprises mixtures of epoxidized Cn-C22-fatty acid-Ci-Ci2-alkyl esters and epoxidized Cn-C22-Fettsäureglyceriden.
Die Fettsäurealkylester können dabei als ein Fettsäurealkylester oder als Mischung von zwei oder mehreren Fettsaurealkylestern vorliegen. Die Fettsaureglyceride können als ein Fettsäureglycerid oder als Mischung von zwei oder mehreren Fettsäureglyceri- den vorliegen. The fatty acid alkyl esters may be present as a fatty acid alkyl ester or as a mixture of two or more fatty acid alkyl esters. The fatty acid glycerides may be present as a fatty acid glyceride or as a mixture of two or more fatty acid glycerides.
Der prozentuale Massenanteil an Sauerstoff, bezogen auf die Gesamtmasse an epoxi- diertem Fettsäure-Ci-Ci2-alkylester und/oder epoxidiertem Fettsäureglycerid, beträgt in einer Ausführung der erfindungsgemäßen Schmierstoffzusammensetzung 3 bis 8 Gew.-%. The percentage by weight of oxygen, based on the total mass of epoxidized fatty acid C 1 -C 12 -alkyl ester and / or epoxidized fatty acid glyceride, in one embodiment of the lubricant composition according to the invention is 3 to 8% by weight.
Die Herstellung der Cn-C22-Fettsäure-Ci-Ci2-alkylester und epoxidierten C11-C22- Fettsäureglyceride erfolgt in üblicher weise, beispielsweise nach dem in J. Am. Chem. Soc. 62 (1945), S. 412-414 beschriebenen Verfahren. Die Bestimmung des Epoxidge- halts erfolgt in üblicher weise, beispielsweise nach der in der EP 1693359 bzw. DIN 16945 beschriebenen Methode. The production of the Cn-C22-fatty acid-Ci-Ci2-alkylester and epoxidized C11-C22-Fettsäureglyceride is carried out in the usual manner, for example according to the in J. Am. Chem. Soc. 62 (1945), pp. 412-414. The determination of the epoxide content is carried out in a customary manner, for example according to the method described in EP 1693359 or DIN 16945.
Die erfindungsgemäße Schmierstoffzusammensetzung umfasst als Komponente c) einen Rost- und/oder Oxidationsinhibitor. Der Rost- und/oder Oxidationsinhibitor ist i der Zusammensetzung im Allgemeinen in einer Menge von 0,05 bis 2 Gew.-%, vorzugsweise 0,05 bis 1 ,0 Gew.-%, enthalten, jeweils bezogen auf das Gesamtgewicht der Zusammensetzung. The lubricant composition of the invention comprises as component c) a rust and / or oxidation inhibitor. The rust and / or oxidation inhibitor is generally contained in the composition in an amount of 0.05 to 2% by weight, preferably 0.05 to 1.0% by weight, based in each case on the total weight of the composition.
In einer Ausführungsform der Erfindung umfasst die Komponente (c) wenigstens ein einfach oder mehrfach C1-C12-Alkyl-substituiert.es Phenol oder wenigstens ein Arylamin oder wenigstens ein einfach oder mehrfach substituiertes Triazol. In einer weiteren Ausführungsform der Erfindung umfasst die Komponente (c) wenigstens ein einfach oder mehrfach C1-C12-Alkyl-substituiert.es Phenol und wenigstens ein Arylamin oder wenigstens ein einfach oder mehrfach substituiertes Triazol. In einer weiteren Ausfüh- rungsform der Erfindung umfasst die Komponente (c) wenigstens ein Arylamin und wenigstens ein einfach oder mehrfach substituiertes Triazol. In einer weiteren Ausführungsform der Erfindung umfasst die Komponente (c) wenigstens ein einfach oder mehrfach C1-C12-Alkyl-substituiert.es Phenol und wenigstens ein Arylamin und wenigstens ein einfach oder mehrfach substituiertes Triazol. In einer Ausführungsform der Erfindung ist das Ci-Ci2-Alkyl-substituierte Phenol der Komponente c) ausgewählt unter Ci-Ci2-Alkyl-substituierten Phenolen mit sterisch anspruchsvollen Substituenten, wie Isopropyl oder tert. -Butyl. Das Phenol kann mit einem Substituenten oder mit 2, 3, 4 oder 5 Substituenten substituiert sein. Vorzugsweise ist das Phenol zweifach oder dreifach substituiert. In one embodiment of the invention, component (c) comprises at least one mono- or polysubstituted C1-C12-alkyl-substituted phenol or at least one arylamine or at least one singly or multiply substituted triazole. In a further embodiment of the invention, component (c) comprises at least one singly or multiply C 1 -C 12 -alkyl-substituted phenol and at least one arylamine or at least one singly or multiply substituted triazole. In a further embodiment of the invention, component (c) comprises at least one arylamine and at least one singly or multiply substituted triazole. In a further embodiment of the invention, component (c) comprises at least one singly or multiply C 1 -C 12 -alkyl-substituted phenol and at least one arylamine and at least one singly or multiply substituted triazole. In one embodiment of the invention, the Ci-Ci2-alkyl-substituted phenol of the component c) is selected from Ci-Ci2-alkyl-substituted phenols with sterically demanding substituents, such as isopropyl or tert. Butyl. The phenol can be substituted with one substituent or with 2, 3, 4 or 5 substituents. Preferably, the phenol is substituted twice or three times.
In einer Ausführungsform sind die Ci-Ci2-Alkyl-substituierten Phenole ausgewählt unter 2,6-Di-tert-butylphenol, 4-Methyl-2,6-di-tert-butylphenol, 2,4,6-Tri-tert-butylphenol, 2- tert-Butylphenol, 2,6-Diisopropylphenol, 2-Methyl-6-tert-butylphenol, 2,4-Dimethyl-6- tert-butylphenol und 4-Ethyl-2,6-di-tert-butylphenol. In one embodiment, the Ci-Ci2-alkyl-substituted phenols are selected from 2,6-di-tert-butylphenol, 4-methyl-2,6-di-tert-butylphenol, 2,4,6-tri-tert-butylphenol , 2-tert-butylphenol, 2,6-diisopropylphenol, 2-methyl-6-tert-butylphenol, 2,4-dimethyl-6-tert-butylphenol and 4-ethyl-2,6-di-tert-butylphenol.
Die Komponente c) kann ein Ci-Ci2-Alkyl-substituiertes Phenol oder eine Mischung von zwei oder mehreren Ci-Ci2-Alkyl-substituierten Phenolen umfassen. Component c) may comprise a C 1 -C 12 -alkyl-substituted phenol or a mixture of two or more C 1 -C 12 -alkyl-substituted phenols.
In einer Ausführungsform der Erfindung umfasst die Komponente c) wenigstens ein Arylamin, das ausgewählt ist unter In one embodiment of the invention, component c) comprises at least one arylamine which is selected from
Alkyldiphenylaminen der allgemeinen Formel (I)
Figure imgf000007_0001
Alkyldiphenylamines of the general formula (I)
Figure imgf000007_0001
wobei R1, R2, R3 und R4 gleich oder verschieden für Wasserstoff oder Ci-Cis-Alkyl stehen, where R 1 , R 2 , R 3 and R 4 are identical or different and represent hydrogen or C 1 -C 6 -alkyl,
Phenyl-a-naphthylaminen der all emeinen Formel (II)  Phenyl-a-naphthylamines of the general formula (II)
Figure imgf000007_0002
wobei R5 für Wasserstoff oder Ci-Cis-Alkyl steht und
Figure imgf000007_0002
wherein R 5 is hydrogen or Ci-Cis-alkyl and
Phenyl-ß-naphthylaminen der allgemeinen Formel (III) Phenyl-.beta.-naphthylamines of the general formula (III)
Figure imgf000008_0001
Figure imgf000008_0001
wobei R6 für Wasserstoff oder Ci-Cis-Alkyl steht. wherein R 6 is hydrogen or Ci-Cis-alkyl.
R1, R2, R3 und R4 können jeweils für Wasserstoff stehen. Vorzugsweise jedoch ist we- nigstens einer der Reste eine Alkylgruppe mit 1 bis 18 Kohlenstoffatomen, insbesondere 8 bis 18 Kohlenstoffatomen. Die Alkylgruppen können linear oder verzweigt sein. Eine solche Alkylgruppe kann eine Methylgruppe, Ethylgruppe, n-Propylgruppe, Isop- ropylgruppe, n-Butylgruppe, sek.-Butylgruppe, tert.-Butylgruppe, Amylgruppe, He- xylgruppe, Heptylgruppe, Octylgruppe, 2-Ethylhexylgruppe, Nonylgruppe, Iso- nonylgruppe, Decylgruppe, Undecylgruppe, Dodecylgruppe, Tridecylgruppe, Isotride- cylgruppe, Tetradecylgruppe, Pentadecylgruppe, Hexadecylgruppe, Heptadecylgruppe, oder Octadecylgruppe sein. R 1 , R 2 , R 3 and R 4 may each stand for hydrogen. Preferably, however, at least one of the radicals is an alkyl group having 1 to 18 carbon atoms, especially 8 to 18 carbon atoms. The alkyl groups may be linear or branched. Such an alkyl group may include a methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, amyl group, hexyl group, heptyl group, octyl group, 2-ethylhexyl group, nonyl group, isononyl group , Decyl, undecyl, dodecyl, tridecyl, isotridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, or octadecyl.
In der allgemeinen Formel (II) ist R5 ein Wasserstoffatom oder eine Alkylgruppe mit 1 bis 18 Kohlenstoffatomen. Vorzugsweise ist R5 eine Alkylgruppe mit 1 bis 18 Kohlenstoffatomen, insbesondere 8 bis 18 Kohlenstoffatomen. Die Alkylgruppe mit 1 bis 18 Kohlenstoffatomen ist wie für R1 bis R4 definiert. In the general formula (II), R 5 is a hydrogen atom or an alkyl group having 1 to 18 carbon atoms. Preferably, R 5 is an alkyl group of 1 to 18 carbon atoms, more preferably 8 to 18 carbon atoms. The alkyl group having 1 to 18 carbon atoms is as defined for R 1 to R 4 .
In der allgemeinen Formel (III) ist R6 ein Wasserstoffatom oder eine Alkylgruppe mit 1 bis 18 Kohlenstoffatomen. Vorzugsweise ist R6 eine Alkylgruppe mit 1 bis 18 Kohlenstoffatomen, insbesondere 8 bis 18 Kohlenstoffatomen. Die Alkylgruppe mit 1 bis 18 Kohlenstoffatomen ist wie für R1 bis R4 definiert. In the general formula (III), R 6 is a hydrogen atom or an alkyl group having 1 to 18 carbon atoms. Preferably, R 6 is an alkyl group of 1 to 18 carbon atoms, more preferably 8 to 18 carbon atoms. The alkyl group having 1 to 18 carbon atoms is as defined for R 1 to R 4 .
Die Komponente c) kann ein Alkyldiphenylamin der allgemeinen Formel (I) allein um- fassen, aber auch Mischungen von zwei oder mehreren Alkyldiphenylaminen der allgemeinen Formel (I). Weiterhin kann die Komponente c) ein Phenyl-alpha- naphthylamin der allgemeinen Formel (II) allein umfassen, oder auch Mischungen von zwei oder mehreren Phenyl-alpha-naphthylaminen (II). Weiterhin kann die Komponente c) ein Phenyl-beta-naphthylamin der allgemeinen Formel (III) allein umfassen, oder auch Mischungen von zwei oder mehreren Phenyl-alpha-naphthylaminen (III). Kompo- nente c) kann zudem Mischungen von zwei oder mehreren der Arylamine (I), (II) und (III) umfassen. Component c) may comprise an alkyldiphenylamine of the general formula (I) alone, but also mixtures of two or more alkyldiphenylamines of the general formula (I). Furthermore, component c) may comprise a phenyl-alphanaphthylamine of general formula (II) alone, or else mixtures of two or more phenyl-alpha-naphthylamines (II). Furthermore, component c) may comprise a phenyl-beta-naphthylamine of the general formula (III) alone, or else mixtures of two or more phenyl-alpha-naphthylamines (III). com- Component c) may additionally comprise mixtures of two or more of the arylamines (I), (II) and (III).
Vorzugsweise sind Mischungen von wenigstens zwei voneinander verschiedenen Arylaminen Bestandteil der Komponente c). Preferably, mixtures of at least two different arylamines are part of component c).
Die Komponente c) kann ein einfach oder mehrfach substituiertes Triazol umfassen. Component c) may comprise a mono- or polysubstituted triazole.
In einer Ausführungsform ist das substituierte Triazol ausgewählt unter Alkyl- und/oder Aryl-substituierten Triazolen, vorzugsweise Ci-Ci2-Alkyl- und/oder C6-Ci8-Aryl- substituierten 1 ,2,3-Triazolen und 1 ,2,4-Triazolen. In one embodiment, the substituted triazole is selected from alkyl- and / or aryl-substituted triazoles, preferably Ci-Ci2-alkyl and / or C6-Ci8-aryl-substituted 1, 2,3-triazoles and 1, 2,4- triazoles.
Unter Ci-Ci2-Alkyl sind lineare, verzweigte oder cyclische Alkylreste mit 1 bis 12 Kohlenstoffatomen zu verstehen. Unter C6-Ci8-Aryl sind aromatische Reste mit 6 bis 18 Kohlenstoffatomen, z.B. einkernige aromatische Reste oder zwei oder mehrkernige aromatische Reste, die anelliert oder über eine chemische Verbindung oder eine Ci- C6-Alkyl brücke verbrückt sein können, zu verstehen. Ci-Ci2-alkyl are linear, branched or cyclic alkyl radicals having 1 to 12 carbon atoms to understand. By C 6 -C 18 aryl are aromatic radicals having 6 to 18 carbon atoms, e.g. mononuclear aromatic radicals or two or more nuclear aromatic radicals which may be fused or bridged by a chemical compound or a Ci- C6-alkyl bridge to understand.
Beispiele für einfach substituierte 1 ,2,4-Triazole sind 1 -Alkyl oder Aryl-substituierte-1 H- 1 ,2,4-Triazole, 3-Alkyl oder Aryl-substituierte-1 H-s-Triazole oder 4-Alkyl oder Aryl- substituierte-4H-1 ,2,4-Triazole. Beispiele für zweifach substituierte 1 ,2,4-Triazole sind 1 ,3-Alkyl und/oder Aryl-disubstituierte-1 H-1 ,2,4-Triazole, 1 ,5-Alkyl und/oder Aryl- disubstituierte-1 H-1 ,2,4-Triazole, 3,4-Alkyl und/oder Aryl-disubstituierte-4H-1 ,2,4- Triazole oder 3,5-Alkyl und/oder Aryl-disubstituierte-s-Triazole. Beispiele für dreifach substituierte 1 ,2,4-Triazole sind 1 , 3,5-Alkyl und/oder Aryl-trisubstituierte-1 H-1 ,2,4- Triazole oder 3,4,5-Alkyl und/oder Aryl-trisubstituierte-4H-1 ,2,4-Triazole. Examples of monosubstituted 1,2,4-triazoles are 1-alkyl or aryl-substituted-1H-1, 2,4-triazoles, 3-alkyl or aryl-substituted-1H-triazoles or 4-alkyl or aryl substituted-4H-1, 2,4-triazoles. Examples of di-substituted 1,2,4-triazoles are 1,3-alkyl and / or aryl-disubstituted-1H-1, 2,4-triazoles, 1,5-alkyl and / or aryl-disubstituted-1H- 1, 2,4-triazoles, 3,4-alkyl and / or aryl-disubstituted-4H-1, 2,4-triazoles or 3,5-alkyl and / or aryl-disubstituted-s-triazoles. Examples of triply substituted 1,2,4-triazoles are 1,3,5-alkyl and / or aryl-trisubstituted-1H-1, 2,4-triazoles or 3,4,5-alkyl and / or aryl-trisubstituted -4H-1, 2,4-triazoles.
Beispiele für einfach substituierte 1 ,2,3-Triazole sind 1 -Alkyl oder Aryl-substituierte-1 H- 1 ,2,3-Triazole oder 2-Alkyl oder Aryl-substituierte-2H-1 ,2,3-Triazole. Beispiele für zwei- fach substituierte 1 ,2,3-Triazole sind 1 ,4-Alkyl und/oder Aryl-disubstituierte-1 H-1 ,2,3- Triazole oder 2,4-Alkyl und/oder Aryl-disubstituierte-2H-1 ,2,3-Triazole. Beispiele für dreifach substituierte 1 ,2,3-Triazole sind 1 ,4,5-Alkyl und/oder Aryl-trisubstituierte-2H- 1 ,2,3-Triazole oder 2,4,5-Alkyl und/oder Aryl-trisubstituierte-1 H-1 ,2,3-Triazole. Geeignete Vertreter der Komponente c) sind im Handel erhältlich. Examples of monosubstituted 1,2,3-triazoles are 1-alkyl or aryl-substituted-1H-1,2,3-triazoles or 2-alkyl or aryl-substituted-2H-1,2,3-triazoles. Examples of di-substituted 1,2,3-triazoles are 1,4-alkyl and / or aryl-disubstituted-1H-1,2,3-triazoles or 2,4-alkyl and / or aryl-disubstituted-2H -1,2,3-triazoles. Examples of triply substituted 1,2,3-triazoles are 1, 4,5-alkyl and / or aryl-trisubstituted-2H-1,2,3-triazoles or 2,4,5-alkyl and / or aryl-trisubstituted 1 H-1,2,3-triazoles. Suitable representatives of component c) are commercially available.
In einer weiteren Ausführungsform umfasst die erfindungsgemäße Zusammensetzung zusätzlich einen Entschäumer. Der Entschäumer kann beispielsweise in einer Menge von 0,001 bis 0,1 Gew.-%, vorzugsweise 0,005 bis 0,05 Gew.-%, bezogen auf die Ge- samtmasse der erfindungsgemäßen Zusammensetzung, in der Zusammensetzung enthalten sein. In a further embodiment, the composition according to the invention additionally comprises a defoamer. The antifoam may be used, for example, in an amount of 0.001 to 0.1% by weight, preferably 0.005 to 0.05% by weight, based on the total composition of the composition according to the invention, be included in the composition.
Als Entschäumer, die als Zusatz zur erfindungsgemäßen Zusammensetzung geeignet sind, kommen Homopolymere von (Meth)-Ci-Ci8-alkylacrylaten, Copolymere von wenigstens zwei (Meth)-Ci-Ci8-alkylacrylaten oder Mischungen davon in Frage. Suitable defoamers which are suitable as an additive to the composition of the invention are homopolymers of (meth) -Ci-Ci8-alkyl acrylates, copolymers of at least two (meth) -Ci-Ci8-alkyl acrylates or mixtures thereof in question.
In einer Ausführungsform werden als Entschäumer Homopolymere von (Meth)-Ci-Cs- alkylacrylaten, Copolymere von wenigstens zwei (Meth)-Ci-C8-alkylacrylaten oder Mi- schungen davon eingesetzt. Alkyl steht dabei für lineare oder verzweigte Alkylgrup- pen, wie Methyl, Ethyl-, Propyl-, n-Butyl-, Isobutyl-, Pentyl-, Hexyl-, 2-Ethylhexyl-, Heptyl- oder Octylgruppen. Bevorzugt sind die Methyl-, Ethyl-, n-Butyl- und 2- Ethylhexylgruppe. Die Polymere können auch weitere Monomere eingebaut enthalten, wie (Meth)acrylsäure, (Meth)acrylamid, Hydroxy-C2-C6-alkyl-(meth)acrylat. In one embodiment, the defoamers used are homopolymers of (meth) -Ci-Cs-alkyl acrylates, copolymers of at least two (meth) -Ci-C8-alkyl acrylates or mixtures thereof. Alkyl stands for linear or branched alkyl groups, such as methyl, ethyl, propyl, n-butyl, isobutyl, pentyl, hexyl, 2-ethylhexyl, heptyl or octyl groups. Preference is given to the methyl, ethyl, n-butyl and 2-ethylhexyl groups. The polymers may also contain other monomers incorporated, such as (meth) acrylic acid, (meth) acrylamide, hydroxy-C 2 -C 6 -alkyl (meth) acrylate.
In einer bevorzugten Ausführungsform werden als Entschäumer Copolymere von wenigstens zwei (Meth)-Ci-C8-alkylacrylaten eingesetzt. Ein Beispiel für derartige Entschäumer sind Copolymere von n-Butylacrylat und/oder 2-Ethylhexylacrylat und Me- thylacrylat und/oder Ethylacrylat. In einer Ausführungsform ist der Entschäumer im Wesentlichen silikonfrei. Im Wesentlichen silikonfrei bedeutet, dass, bezogen auf die Gesamtmasse des Entschäumers, weniger als 1 Gew.-%, bevorzugt 0 Gew.-%, an Silikonen im Entschäumer enthalten ist. Geeignete Entschäumer sind im Handel erhältlich. In a preferred embodiment, copolymers of at least two (meth) -Ci-C8-alkyl acrylates are used as antifoams. An example of such defoamers are copolymers of n-butyl acrylate and / or 2-ethylhexyl acrylate and methyl acrylate and / or ethyl acrylate. In one embodiment, the defoamer is substantially free of silicone. Substantially silicone-free means that, based on the total mass of the defoamer, less than 1% by weight, preferably 0% by weight, of silicones is contained in the defoamer. Suitable defoamers are commercially available.
In einer weiteren Ausführungsform umfasst die erfindungsgemäße Zusammensetzung zusätzlich einen Hochdruckzusatz (extreme pressure agent). Der Hochdruckzusatz kann beispielsweise in einer Menge von 0,001 bis 0,1 Gew.-%, vorzugsweise 0,002 bis 0,03 Gew.-%, bezogen auf die Gesamtmasse der erfindungsgemäßen Zusammensetzung, in der Zusammensetzung enthalten sein. In a further embodiment, the composition according to the invention additionally comprises an extreme pressure agent. The high pressure additive can be contained in the composition, for example, in an amount of 0.001 to 0.1 wt .-%, preferably 0.002 to 0.03 wt .-%, based on the total mass of the composition according to the invention.
Hochdruckzusätze, die als Zusatz zur erfindungsgemäßen Zusammensetzung geeignet sind, sind im Allgemeinen öllöslich. Geeignete Hochdruckzusätze sind beispiels- weise ausgewählt unter öllöslichen organischen Estern der Phosphorsäure, öllöslichen organischen Estern der Phosphinsäure, öllöslichen organischen Estern der Phosphon- säure, öllöslichen organischen Estern der Schwefelsäure, öllöslichen organischen Estern der Schwefligen Säure, öllöslichen organischen Estern der Sulfonsäure, Aminsalzen von Hydroxy-substituierten Phosphetanen, Aminsalzen von Hydroxy-substituierten Thiophosphetanen, Aminsalzen von Partialestern der phosphorigen Säure und Amin- salzen von Partialestern der thiophosphorigen Säure. High pressure additives useful as an additive to the composition of the present invention are generally oil soluble. Suitable high-pressure additives are selected, for example, from oil-soluble organic esters of phosphoric acid, oil-soluble organic esters of phosphinic acid, oil-soluble organic esters of phosphonic acid, oil-soluble organic esters of sulfuric acid, oil-soluble organic esters of sulfurous acid, oil-soluble organic esters of sulfonic acid, amine salts of hydroxy -substituted phosphetanes, amine salts of hydroxy-substituted Thiophosphetanen, amine salts of partial esters of phosphorous acid and amine salts of partial esters of thiophosphorigenic acid.
Phosphorsäure, Phosphinsäure, Phosphonsäure, Schwefelsäure, schwefligen Säure und Sulfonsäure sind dabei beispielsweise mit Alkoholen mit z.B. 4 bis 18 Kohlenstoffatomen verestert. Phosphoric acid, phosphinic acid, phosphonic acid, sulfuric acid, sulfurous acid and sulfonic acid are, for example, with alcohols with e.g. 4 to 18 carbon atoms esterified.
Unter den Aminsalzen von Hydroxy-substituierten Phosphetanen, Hydroxy- substituierten Thiophosphetanen, Partialestern der phosphorigen Säure und Partia- lestern der thiophosphorigen Säure sind beispielsweise die C6-Ci2-Alkylaminsalze davon zu verstehen, vorzugsweise die Octylaminsalze davon. Examples of amine salts of hydroxy-substituted phosphetanes, hydroxy-substituted thiophosphetanes, partial esters of phosphorous acid and partial esters of thiophosphorous acid are the C 6 -C 12 -alkylamine salts thereof, preferably the octylamine salts thereof.
Partialester der phosphorigen Säure und der thiophosphorigen Säure sind nicht an allen OH-Gruppen der zugrundeliegenden freien Säuren vollständig verestert. Die teil- weise Veresterung der phosphorigen Säure und der thiophosphorigen Säure kann beispielsweise mit Alkoholen mit z.B. 4 bis 18 Kohlenstoffatomen erfolgen. Partial esters of phosphorous acid and thiophosphorous acid are not completely esterified at all OH groups of the underlying free acids. The partial esterification of the phosphorous acid and the thiophosphorous acid can be carried out, for example, with alcohols with e.g. 4 to 18 carbon atoms take place.
In einer bevorzugten Ausführungsform umfasst die erfindungsgemäße Zusammensetzung einen Hochdruckzusatz, der unter Alkylthiophosphatestern ausgewählt ist. In a preferred embodiment, the composition of the invention comprises a high pressure additive selected from alkyl thiophosphate esters.
Beispiele für Alkylthiophosphatester sind Ci-Cis-Alkylester der Thiophosphorsäure. Die Alkylthiophosphorsäureester können dabei drei identische Alkylreste aufweisen, zwei oder drei voneinander verschiedene. Geeignete Hochdruckzusätze sind im Handel erhältlich. Examples of alkyl thiophosphate esters are C 1 -C 6 -alkyl esters of thiophosphoric acid. The alkylthiophosphoric acid esters may have three identical alkyl radicals, two or three different from one another. Suitable high pressure additives are commercially available.
In einer Ausführungsform umfasst die erfindungsgemäße Schmierstoffzusammensetzung einen Hochdruckzusatz oder ein Gemisch von zwei oder mehreren, voneinander verschiedenen Hochdruckzusätzen. In one embodiment, the lubricant composition of the invention comprises a high pressure additive or a mixture of two or more high pressure additives different from each other.
In einer bevorzugten Ausführungsform der Erfindung umfasst die Schmierstoffzusammensetzung wenigstens einen Entschäumer und wenigstens einen Hochdruckzusatz, wobei der Entschäumer und der Hochdruckzusatz wie oben definiert sind. In einer weiteren Ausführungsform umfasst die erfindungsgemäße Schmierstoffzusammensetzung a) das Grundöl mit einer Viskosität von 30 bis 70 mm2/s bei 40 °C, insbesondere ein Hydrocracköl mit einer Viskosität von 40 bis 50 mm2/s bei 40 °C, b) 0,05 bis 1 ,5 Gew.-%, insbesondere 0,05 bis 0,9 Gew.-%, der Hydrolyseschutzkomponente, c) 0,05 bis 2 Gew.-%, insbesondere 0,05 bis 1 ,0 Gew.-%, des Rost- und Oxida- tionsinhibitors, d) gegebenenfalls 0,001 bis 0,1 Gew.-%, insbesondere 0,005 bis 0,05 Gew.-%, eines Entschäumers, und e) gegebenenfalls 0,001 bis 0,1 Gew.-%, insbesondere 0,002 bis 0,03 Gew.-%, eines Hochdruckzusatzes, jeweils bezogen auf das Gesamtgewicht der Zusammensetzung, wobei die Kompo- nenten a) bis e) wie oben definiert sind. In a preferred embodiment of the invention, the lubricant composition comprises at least one defoamer and at least one high pressure additive, wherein the defoamer and the high pressure additive are as defined above. In a further embodiment, the lubricant composition according to the invention comprises a) the base oil having a viscosity of 30 to 70 mm 2 / s at 40 ° C., in particular a hydrocracker oil having a viscosity of 40 to 50 mm 2 / s at 40 ° C., b) 0.05 to 1, 5 wt .-%, in particular 0.05 to 0.9 wt .-%, of the hydrolysis protection component, c) 0.05 to 2 wt .-%, in particular 0.05 to 1, 0 D) optionally from 0.001 to 0.1% by weight, in particular from 0.005 to 0.05% by weight, of an antifoam, and e) optionally from 0.001 to 0.1% by weight of the rust and oxidation inhibitor; .-%, in particular 0.002 to 0.03 wt .-%, of a high pressure additive, each based on the total weight of the composition, wherein the components a) to e) are as defined above.
In einer weiteren Ausführungsform enthalten die erfindungsgemäßen Schmierstoffzusammensetzungen keinen Bernsteinsäureester und/oder kein Asparaginsäurederivat, insbesondere keine am Stickstoffatom acylierte Asparaginsäure oder einen Ester da- von. Die Bernsteinsäureester entsprechen der Formel In a further embodiment, the lubricant compositions according to the invention contain no succinic acid ester and / or no aspartic acid derivative, in particular no aspartic acid acylated on the nitrogen atom or an ester thereof. The succinic esters correspond to the formula
Figure imgf000012_0001
worin Xi und X2 unabhängig voneinander für H oder Alkyl, Alkenyl oder Hydroxyalkyl mit 3 bis 6 Kohlenstoffatomen stehen und X3 1 bis 30 Kohlenstoffatome aufweist und für Alkyl, Alkenyl, Alkyl mit Etherbindungen oder Hydroxyalkyl steht,
Figure imgf000012_0001
wherein Xi and X2 independently of one another are H or alkyl, alkenyl or hydroxyalkyl having 3 to 6 carbon atoms and X3 has 1 to 30 carbon atoms and is alkyl, alkenyl, alkyl having ether bonds or hydroxyalkyl,
die Asparaginsäurederivate entsprechen der Formel the aspartic acid derivatives correspond to the formula
Figure imgf000012_0002
Figure imgf000012_0002
worin Xi und X2 für H, Alkyl oder Hydroxyalkyl mit 3 bis 6 Kohlenstoffatomen stehen, X3 für Alkyl mit 1 bis 30 Kohlenstoffatomen, Alkyl mit Etherbindungen oder Hydroxyalkyl steht und X4 für gesättigte oder ungesättigte Carbonsäuregruppen aufweisende Reste, insbesondere Alkyl- oder Alkenylreste, mit 1 bis 30 Kohlenstoffatomen, Alkenyl oder Hydroxyalkyl steht. Die erfindungsgemäßen Schmierstoffzusammensetzungen weisen den Vorteil einer hohen Beständigkeit gegen Chlor oder chlorhaltige Produkte auf. Insbesondere sind die erfindungsgemäßen Schmierstoffzusammensetzungen beständig gegen Chlorgeh- alte von über 50 ppm bis zu 2000 ppm. Damit sind die erfindungsgemäßen Schmierstoffzusammensetzungen für die Schmierung von Turbinen oder (Turbo)kompressoren, die zur Verdichtung von Chlor und/oder chlorhaltigen Produkten dienen, geeignet. wherein Xi and X2 are H, alkyl or hydroxyalkyl having 3 to 6 carbon atoms, X3 is alkyl having 1 to 30 carbon atoms, alkyl having ether bonds or hydroxyalkyl and X 4 for saturated or unsaturated carboxylic acid groups having radicals, in particular alkyl or alkenyl radicals, with 1 to 30 carbon atoms, alkenyl or hydroxyalkyl. The lubricant compositions according to the invention have the advantage of high resistance to chlorine or chlorine-containing products. In particular, the lubricant compositions according to the invention are resistant to chlorine contents of more than 50 ppm up to 2000 ppm. Thus, the lubricant compositions according to the invention for the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products are suitable.
Gegenstand der Erfindung ist weiterhin die Verwendung der erfindungsgemäßen Schmierstoffzusammensetzungen zur Schmierung von Turbinen oder (Tur- bo)kompressoren. The invention further relates to the use of the lubricant compositions according to the invention for the lubrication of turbines or (turbo) compressors.
Die erfindungsgemäßen Schmierstoffzusammensetzungen sind dabei besonders für die Verwendung zur Schmierung von Turbinen oder (Turbo)kompressoren, die zur Verdichtung von Chlor und/oder chlorhaltigen Produkten dienen, geeignet. The lubricant compositions according to the invention are particularly suitable for use in the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products.
Die erfindungsgemäßen Schmierstoffzusammensetzungen werden beispielsweise durch Vermischen (unter Verwendung eines geeigneten Rührers) der oben genannten Komponenten in einer geeigneten Vorrichtung, z.B. einem Mischkessel, erhalten. Das Auftragen der Zusammensetzungen auf die zu schmierenden Teile, z.B. Durchführungen für Hubbewegungen einer Turbine oder eines (Turbo)kompressors kann beispielsweise durch Aufspritzen und/oder Verstreichen der Zusammensetzungen auf den genannten Teilen erfolgen. Die nachfolgenden Beispiele dienen zur Erläuterung der Erfindung ohne sie zu begrenzen. The lubricant compositions of the invention are prepared, for example, by mixing (using a suitable stirrer) the above components in a suitable device, e.g. a mixing kettle, received. Applying the compositions to the parts to be lubricated, e.g. Feedthroughs for strokes of a turbine or a (turbo) compressor can be done, for example, by spraying and / or spreading of the compositions on said parts. The following examples serve to illustrate the invention without limiting it.
Beispiel 1 Die folgenden Komponenten wurden in den angegebenen Mengenverhältnissen in einen Mischkessel gegeben und darin zu einer Schmierstoffzusammensetzung vermischt. a) 87,5 Gew.-%, bezogen auf die Gesamtmasse der Zusammensetzung, eines Hyd- rocracköls mit einer Viskosität von 40 bis 55 mm2/s bei 40 °C; b) 1 1 ,6 Gew.-% einer Formulierung, bezogen auf die Gesamtmasse der Zusammensetzung, die etwa 4 Gew.-% wenigstens eines epoxidierten C11-C22- Fettsäure-Ci-Ci2-alkylesters auf Basis von Rapsöl mit einem Gesamtepoxid- sauerstoffgehalt von etwa 7 Gew.-% enthält (Rest Rapsöl); c) 0,8 Gew.-%, bezogen auf die Gesamtmasse der Zusammensetzung, einer For- mulierung, die etwa 15 Gew.-% 2-tert-Butylphenol und Phenyl-a-naphthylaminExample 1 The following components were charged in the proportions indicated in a mixing vessel and mixed therein to form a lubricant composition. a) 87.5% by weight, based on the total mass of the composition, of a hydraulic oil with a viscosity of 40 to 55 mm 2 / s at 40 ° C .; b) 1 1, 6 wt .-% of a formulation, based on the total mass of the composition containing about 4 wt .-% of at least one epoxidized C11-C22- Fatty acid C 1 -C 12 -alkyl ester based on rapeseed oil with a total oxygen content of about 7% by weight (remainder rapeseed oil); c) 0.8% by weight, based on the total weight of the composition, of a formulation containing about 15% by weight of 2-tert-butylphenol and phenyl-a-naphthylamine
(Gewichtsverhältnis 2:1 ) enthält (Rest Öl); und d) 0, 1 Gew.-%, bezogen auf die Gesamtmasse der Zusammensetzung, wenigstens eines polymeren Entschäumers (Rest Öl). (Weight ratio 2: 1) contains (balance oil); and d) 0, 1 wt .-%, based on the total weight of the composition, of at least one polymeric defoamer (balance oil).
Bestimmung der Korrosionsschutzeigenschaften und der Beständigkeit gegenüber Chlor: Determination of corrosion protection properties and resistance to chlorine:
Zur Bestimmung der korrosionsschützenden Eigenschaften wurde eine in der Schmier- stoffbranche übliche Methode zur Bestimmung der Korrosion nach DI N ISO 7120 modifiziert. Anstelle von Wasser und Öl wurde eine mit 2000 ppm Chlor versetzte Schmierstoffzusammensetzung gemäß Beispiel 1 als Prüfflüssigkeit vorgelegt und die verwendeten Prüfkörper über 24 Stunden bei 60 °C unter Rühren (1000 U/min) belassen. Als Prüfkörper wurden sowohl die in DIN ISO 7120 beschriebenen Prüfkörper aus Stahl, als auch aus Weißmetall verwendet, das üblicherweise als Lagermetall in Kompressoren eingesetzt wird. Nach 24 Stunden wurde der Rührvorgang beendet und die Prüfkörper wurden aus der Prüfflüssigkeit herausgenommen. Nach dem Abtropfen wurde der Prüfkörper mit Reinigungslösung abgespült und der Korrosionsgrad nach der DI N ISO 7120-Klassifikation beurteilt. Ein Prüfkörper gilt als angerostet, wenn irgendein Rostpunkt oder Roststreifen sichtbar ist. Sind beide Prüfkörper rostfrei, hat die To determine the anti-corrosive properties, a standard method for the determination of corrosion according to DI N ISO 7120 was modified in the lubricant industry. Instead of water and oil, a 2000 ppm chlorine offset lubricant composition according to Example 1 was presented as a test liquid and the test specimens used for 24 hours at 60 ° C with stirring (1000 rev / min) left. The specimens used were both the specimens described in DIN ISO 7120 made of steel, and of white metal, which is usually used as a bearing metal in compressors. After 24 hours, the stirring was stopped and the test pieces were taken out of the test liquid. After draining, the test piece was rinsed with cleaning solution and the degree of corrosion was assessed according to the DI N ISO 7120 classification. A specimen is considered rusted if any rust or rust streak is visible. Are both specimens stainless, the
Schmierstoffzusammensetzung die Prüfung bestanden. Lubricant composition passed the test.
Rostfrei: Kein Rostpunkt oder Roststreifen sichtbar Stainless: No rust or rust marks visible
Leichter Rost: Nicht mehr als 6 Rostflecken von je höchstens 1 mm Durchmesser Mäßiger Rost: Mehr Rost als bei leichtem Rost, der jedoch weniger als 5% der  Light rust: Not more than 6 rust spots of 1 mm diameter or less. Moderate rust: More rust than light rust, but less than 5% of rust
Oberfläche der Prüfkörper bedeckt  Surface of the test specimen covered
Starker Rost: Der Rost bedeckt mehr als 5% der Oberfläche der Prüfkörper. Strong rust: The rust covers more than 5% of the surface of the specimens.
Auswertung der Versuche: Evaluation of the experiments:
Es hat sich gezeigt, dass mit der Schmierstoffzusammensetzung gemäß Beispiel 1 selbst bei einer Konzentration von 2000 ppm Chlor im Öl keine Korrosion zu beobachten ist, d.h. die Schmierstoffzusammensetzung hat die Prüfung bestanden. Darüber hinaus war die Schmierstoffzusammensetzung weder verfärbt noch waren Ausfällungen zu beobachten. Die Schmierstoffzusammensetzung hat sich somit selbst gegenüber einem Chlorgehalt von 2000 ppm als beständig erwiesen. It has been found that with the lubricant composition according to Example 1, even at a concentration of 2000 ppm chlorine in the oil no corrosion is observed, ie the lubricant composition has passed the test. In addition, the lubricant composition was neither discolored nor precipitated. The lubricant composition has thus proved to be resistant even to a chlorine content of 2000 ppm.

Claims

Patentansprüche claims
1. Schmierstoffzusammensetzung umfassend (a) ein Grundöl mit einer Viskosität von 30 bis 70 mm2/s bei 40 °C, A lubricant composition comprising (a) a base oil having a viscosity of 30 to 70 mm 2 / s at 40 ° C,
(b) eine Hydrolyseschutzkomponente, umfassend wenigstens einen epoxidierten Cn-C22-Fettsäure-Ci-Ci2-Alkylester und/oder wenigstens ein epoxidiertes Cn- C22-Fettsäureglycerid, mit einem Epoxidsauerstoffgehalt von 1 bis 10 Gew.-%, bezogen auf die Gesamtmasse an epoxidiertem Fettsäure-Ci-Ci2-alkylester und/oder epoxidiertem Fettsäureglycerid, und (B) a hydrolysis protective component comprising at least one epoxidized Cn-C22 fatty acid Ci-Ci2-alkyl ester and / or at least one epoxidized Cn-C22 fatty acid glyceride, having an epoxy oxygen content of 1 to 10 wt .-%, based on the total mass epoxidized fatty acid C 1 -C 12 -alkyl ester and / or epoxidized fatty acid glyceride, and
(c) einen Rost- und Oxidationsinhibitor, ausgewählt unter wenigstens einem einfach oder mehrfach Ci-Ci2-Alkyl-substituierten Phenol, wenigstens einem Aryla- min und wenigstens einem einfach oder mehrfach substituierten Triazol und Gemischen aus zwei oder mehreren dieser Komponenten. (C) a rust and oxidation inhibitor selected from at least one single or multiple Ci-Ci2-alkyl-substituted phenol, at least one arylamine and at least one mono- or polysubstituted triazole and mixtures of two or more of these components.
2. Zusammensetzung nach Anspruch 1 , enthaltend 0,05 bis 1 ,5 Gew.-% der Komponente (b). 2. Composition according to claim 1, containing 0.05 to 1, 5 wt .-% of component (b).
3. Zusammensetzung nach Anspruch 1 oder 2, enthaltend 0,05 bis 2 Gew.-% der Komponente (c), jeweils bezogen auf das Gesamtgewicht der Zusammensetzung. 3. Composition according to claim 1 or 2, containing 0.05 to 2 wt .-% of component (c), each based on the total weight of the composition.
4. Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei die 4. The composition according to any one of the preceding claims, wherein the
Grundolkomponente einen Viskositätsindex von > 120 aufweist.  Grundolkomponente has a viscosity index of> 120.
5. Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei die 5. A composition according to any one of the preceding claims, wherein the
Grundolkomponente (a) wenigstens ein Hydrocracköl umfasst.  Grundolkomponente (a) comprises at least one hydrocrack oil.
6. Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Komponente (a) zusätzlich mindestens eine weitere Grundolkomponente ausgewählt unter Mineralölen, Naturölen, hydrierten Polyolefinölen, Poly-a-Olefinen, Al- kylestern von Dicarbonsäuren, Estern von Dicarbonsäuren mit einem Polyglycol und einem C6-Ci8-Alkohol, C6-Ci8-Alkylestern von Carbonsäuren, C6-C18-6. The composition according to any one of the preceding claims, wherein the component (a) additionally at least one other Grundolkomponente selected from mineral oils, natural oils, hydrogenated polyolefin oils, poly-α-olefins, alkyl esters of dicarboxylic acids, esters of dicarboxylic acids with a polyglycol and a C6 -Ci8-alcohol, C6-Ci8-alkyl esters of carboxylic acids, C6-C18-
Alkylestern von phosphorigen Säuren und Fluorkohlenwasserstofföle umfasst. Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Fettsäure der Fettsäurealkylester und Fettsäureglyceride der Komponente (b) ausgewählt ist unter den Sojabohnenol, Distelöl, Traubenkernol, Senföl, Korianderöl, Leinöl, Rüböl, Borretschöl, Tungöl, Nachtkerzenöl, Walnussöl, Hanföl, Sonnenblumenöl, Olivenöl, Palmöl, Erdnussöl, Kokosnussöl, Ricinusöl oder Fischöl zugrundeliegenden Fettsäuren. Alkyl esters of phosphorous acids and hydrofluorocarbon oils. A composition according to any one of the preceding claims wherein the fatty acid of the fatty acid alkyl esters and fatty acid glycerides of component (b) is selected from soybean oil, thistle oil, grapeseed oil, mustard oil, coriander oil, linseed oil, rapeseed oil, borage oil, tung oil, evening primrose oil, walnut oil, hemp oil, sunflower oil, olive oil , Palm oil, peanut oil, coconut oil, castor oil or fish oil based fatty acids.
8. Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei der Cn- C22-Fettsäure-Ci-Ci2-alkylester ein Cn-C22-Fettsäure-C6-Cio-alkylester ist. 8. The composition according to any one of the preceding claims, wherein the Cn-C22 fatty acid Ci-Ci2-alkyl ester is a Cn-C22 fatty acid C6-Cio-alkyl ester.
Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Komponente (c) umfasst: A composition according to any one of the preceding claims, wherein component (c) comprises:
i) wenigstens ein einfach oder mehrfach Ci-Ci2-Alkyl-substituiertes Phenol und wenigstens ein Arylamin oder wenigstens ein einfach oder mehrfach substituiertes Triazol;  i) at least one mono- or poly-C 1 -C 12 -alkyl-substituted phenol and at least one arylamine or at least one singly or multiply substituted triazole;
ii) wenigstens ein Arylamin und wenigstens ein einfach oder mehrfach substituiertes Triazol; oder  ii) at least one arylamine and at least one singly or multiply substituted triazole; or
iii) wenigstens ein einfach oder mehrfach Ci-Ci2-Alkyl-substituiertes Phenol und wenigstens ein Arylamin und wenigstens ein einfach oder mehrfach substituiertes Triazol.  iii) at least one singly or multiply Ci-Ci2-alkyl-substituted phenol and at least one arylamine and at least one singly or multiply substituted triazole.
10 Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei das Ci- Ci2-Alkyl-substituierte Phenol der Komponente (c) ausgewählt ist unter 2,6-Di- tert-butylphenol, 4-Methyl-2,6-di-tert-butylphenol, 2,4,6-Tri-tert-butylphenol, 2-tert- Butylphenol, 2,6-Diisopropylphenol, 2-Methyl-6-tert-butylphenol, 2,4-Dimethyl-6- tert-butylphenol und 4-Ethyl-2,6-di-tert-butylphenol. A composition according to any one of the preceding claims, wherein the C 1 -C 12 alkyl-substituted phenol of component (c) is selected from 2,6-di-tert-butylphenol, 4-methyl-2,6-di-tert-butylphenol, 2,4,6-tri-tert-butylphenol, 2-tert-butylphenol, 2,6-diisopropylphenol, 2-methyl-6-tert-butylphenol, 2,4-dimethyl-6-tert-butylphenol and 4-ethyl 2,6-di-tert-butyl phenol.
1 1 Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei das Arylamin der Komponente (c) ausgewählt ist unter Alkyldiphenylaminen der allgemeinen Formel (I)
Figure imgf000017_0001
wobei R1, R2, R3 und R4 gleich oder verschieden für Wasserstoff oder C1-C18- Alkyl stehen, Phenyl-a-naphthylaminen der allgemeinen Formel (II) wobei R5 für Wasserstoff oder Ci-Cis-Alkyl steht und Phenyl-ß-naphthylaminen der allgemeinen Formel (III)
A composition according to any one of the preceding claims wherein the arylamine of component (c) is selected from alkyldiphenylamines of general formula (I)
Figure imgf000017_0001
where R 1 , R 2 , R 3 and R 4 are identical or different and denote hydrogen or C 1 -C 18 -alkyl, phenyl-a-naphthylamines of the general formula (II) where R 5 is hydrogen or C 1 -C 6 -alkyl and phenyl-β-naphthylamines of the general formula (III)
Figure imgf000018_0001
Figure imgf000018_0001
(Iii),  (III)
wobei R6 für Wasserstoff oder Ci-Cis-Alkyl steht. wherein R 6 is hydrogen or Ci-Cis-alkyl.
12. Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei das substituierte Triazol ausgewählt ist unter 1 ,2,3-Triazolen und 1 ,2,4-Triazolen, die mit Ci-Ci2-Alkyl und/oder C6-Ci8-Aryl substituiert sind. 12. The composition according to any one of the preceding claims, wherein the substituted triazole is selected from 1, 2,3-triazoles and 1, 2,4-triazoles, which are substituted by Ci-Ci2-alkyl and / or C6-Ci8-aryl.
Zusammensetzung nach einem der vorhergehenden Ansprüche zusätzlich u fassend einen Entschäumer. Composition according to one of the preceding claims, additionally comprising a defoamer.
14. Zusammensetzung nach Anspruch 13, wobei der Entschäumer ausgewählt ist unter Homopolymeren von (Meth)-Ci-Ci8-alkylacrylaten, Copolymeren von wenigstens zwei (Meth)-Ci-Ci8-alkylacrylaten oder Mischungen davon. 14. The composition of claim 13, wherein the defoamer is selected from homopolymers of (meth) -Ci-Ci8-alkyl acrylates, copolymers of at least two (meth) -Ci-Ci8-alkyl acrylates or mixtures thereof.
15. Zusammensetzung nach Anspruch 13 oder 14, umfassend 0,001 bis 0,1 Gew.-% des Entschäumers, bezogen auf das Gesamtgewicht der Zusammensetzung. A composition according to claim 13 or 14 comprising from 0.001 to 0.1% by weight of the defoamer, based on the total weight of the composition.
16. Zusammensetzung nach einem der vorhergehenden Ansprüche zusätzlich umfassend wenigstens einen Hochdruckzusatz, ausgewählt unter öllöslichen organischen Estern der Phosphorsäure, öllöslichen organischen Estern der Phos- phinsäure, öllöslichen organischen Estern der Phosphonsäure, öllöslichen orga- nischen Estern der Schwefelsäure, öllöslichen organischen Estern der Schwefli- gen Säure, öllöslichen organischen Estern der Sulfonsaure, Aminsalzen von Hyd- roxy-substituierten Phosphetanen, Aminsalzen von Hydroxy-substituierten Thio- phosphetanen, Aminsalzen von Partialestern der Phosphorigen Säure und Aminsalzen von Partialestern der Thiophosphorigen Säure. 16. Composition according to one of the preceding claims additionally comprising at least one high pressure additive selected from oil-soluble organic esters of phosphoric acid, oil-soluble organic esters of phosphonic acid, oil-soluble organic esters of phosphonic acid, oil-soluble organic esters of sulfuric acid, oil-soluble organic esters of sulfuric acid. acid, oil-soluble organic esters of sulfonic acid, amine salts of hydroxy-substituted phosphetanes, amine salts of hydroxy-substituted thiophosphetanes, amine salts of partial esters of phosphorous acid and amine salts of partial esters of thiophosphoric acid.
Zusammensetzung nach Anspruch 16, wobei der Hochdruckzusatz unter Al- kylthiophosphatestern ausgewählt ist. A composition according to claim 16, wherein the high pressure additive is selected from alkyl thiophosphate esters.
Zusammensetzung nach Anspruch 16 oder 17, umfassend 0,001 bis 0,1 Gew.-% des Hochdruckzusatzes, bezogen auf das Gesamtgewicht der Zusammensetzung. A composition according to claim 16 or 17 comprising from 0.001 to 0.1% by weight of the high pressure additive, based on the total weight of the composition.
Zusammensetzung nach einem der vorhergehenden Ansprüche, umfassend a) das Grundöl mit einer Viskosität von 30 bis 70 mm2/s bei 40 °C, insbesondere ein Hydrocracköl mit einer Viskosität von 40 bis 50 mm2/s bei 40 °C, b) 0,05 bis 1 ,5 Gew.-%, insbesondere 0,05 bis 0,9 Gew.-%, der Hydrolyseschutzkomponente, c) 0,05 bis 2 Gew.-%, insbesondere 0,05 bis 1 ,0 Gew.-%, des Rost- und Oxi- dationsinhibitors, d) gegebenenfalls 0,001 bis 0,1 Gew.-%, insbesondere 0,005 bis 0,05 Gew.- %, eines Entschäumers, und e) gegebenenfalls 0,001 bis 0,1 Gew.-%, insbesondere 0,002 bis 0,03 Gew.- %, eines Hochdruckzusatzes, jeweils bezogen auf das Gesamtgewicht der Zusammensetzung. Composition according to one of the preceding claims, comprising a) the base oil having a viscosity of 30 to 70 mm 2 / s at 40 ° C, in particular a hydrocracking oil having a viscosity of 40 to 50 mm 2 / s at 40 ° C, b) 0 , 05 to 1, 5 wt .-%, in particular 0.05 to 0.9 wt .-%, of the hydrolysis protection component, c) 0.05 to 2 wt .-%, in particular 0.05 to 1, 0 wt. d) optionally from 0.001 to 0.1% by weight, in particular from 0.005 to 0.05% by weight, of an antifoam, and e) optionally from 0.001 to 0.1% by weight , in particular 0.002 to 0.03% by weight, of a high pressure additive, in each case based on the total weight of the composition.
Zusammensetzung nach einem der vorhergehenden Ansprüche, die im wesentlichen keinen Bernsteinsäureester enthält. 21 . Verwendung der Schmierstoffzusammensetzung nach einem der vorhergehenden Ansprüche zur Schmierung von Turbinen oder (Turbo)kompressoren. 22. Verwendung der Schmierstoffzusammensetzung nach Anspruch 20 zur Schmierung von Turbinen oder (Turbo)kompressoren, die zur Verdichtung von Chlor und/oder Chlor-haltigen Produkten dienen. A composition according to any one of the preceding claims, which contains substantially no succinic acid ester. 21. Use of the lubricant composition according to any one of the preceding claims for the lubrication of turbines or (turbo) compressors. 22. Use of the lubricant composition according to claim 20 for the lubrication of turbines or (turbo) compressors, which serve for the compression of chlorine and / or chlorine-containing products.
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