WO2017050982A1 - Compositions lubrifiantes - Google Patents

Compositions lubrifiantes 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)
English (en)
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 US15/761,763 priority Critical patent/US20190085259A1/en
Priority to CN201680056512.7A priority patent/CN108138073A/zh
Priority to EP16770284.4A priority patent/EP3353271B1/fr
Publication of WO2017050982A1 publication Critical patent/WO2017050982A1/fr

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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
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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
    • 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
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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
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
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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
    • 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
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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
    • C10M129/04Hydroxy compounds
    • C10M129/10Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
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    • 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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    • 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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    • 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
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    • 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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    • 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.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Lubricants (AREA)

Abstract

La présente invention concerne des compositions lubrifiantes qui sont adaptées en particulier pour lubrifier des turbines ou des (turbo)compresseurs qui servent à comprimer du chlore et/ou des produits contenant du chlore. Une composition lubrifiante selon l'invention comprend une huile de base, un composant de protection contre l'hydrolyse, ainsi qu'un antirouille et un antioxydant.
PCT/EP2016/072719 2015-09-25 2016-09-23 Compositions lubrifiantes WO2017050982A1 (fr)

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US15/761,763 US20190085259A1 (en) 2015-09-25 2016-09-23 Lubricant compositions
CN201680056512.7A CN108138073A (zh) 2015-09-25 2016-09-23 润滑剂组合物
EP16770284.4A EP3353271B1 (fr) 2015-09-25 2016-09-23 Compositions de lubrifiant

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