EP0919607A2 - Lubrifiant d'usinage mécanique de matériaux et additif pour lubrifiant - Google Patents

Lubrifiant d'usinage mécanique de matériaux et additif pour lubrifiant Download PDF

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Publication number
EP0919607A2
EP0919607A2 EP98122266A EP98122266A EP0919607A2 EP 0919607 A2 EP0919607 A2 EP 0919607A2 EP 98122266 A EP98122266 A EP 98122266A EP 98122266 A EP98122266 A EP 98122266A EP 0919607 A2 EP0919607 A2 EP 0919607A2
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EP
European Patent Office
Prior art keywords
lubricant
phenyl
alkyl
additive
butanol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP98122266A
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German (de)
English (en)
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EP0919607A3 (fr
Inventor
Berndt Dr. Singer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rhenus Lub GmbH and Co KG
Original Assignee
Rhenus Lub GmbH and Co KG
Rhenus Wilhelm Reiners GmbH and Co
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Filing date
Publication date
Application filed by Rhenus Lub GmbH and Co KG, Rhenus Wilhelm Reiners GmbH and Co filed Critical Rhenus Lub GmbH and Co KG
Publication of EP0919607A2 publication Critical patent/EP0919607A2/fr
Publication of EP0919607A3 publication Critical patent/EP0919607A3/fr
Withdrawn legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • C10M129/06Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • 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
    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/044Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • 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
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
    • 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
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/107Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
    • 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
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/107Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
    • C10M2209/1075Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106 used as base material
    • 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
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/108Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/16Antiseptic; (micro) biocidal or bactericidal
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/24Emulsion properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/01Emulsions, colloids, or micelles

Definitions

  • the present invention relates to a lubricant for the mechanical processing or processing of materials with the features of the preamble of claim 1 and Additive for such a lubricant.
  • Lubricants to which an additive for physical and / or Microbiological stabilization have been added since known for a long time.
  • these additives serve the liquid or viscous lubricant, which is usually systems containing oil or fat or emulsions thereof acts to impart targeted properties.
  • additives such as 2-phenoxyalkanols
  • 2-phenoxyalkanols can be used for lubricants or cooling lubricants good tribological properties, so in particular good lubrication, cooling and flushing effects.
  • One via such an additive, in particular one via one 2-phenoxyethanol, stabilized composition has the Advantage on the related oil or fat composition or an emulsion made from it their physical stabilization by the additive has a long service life of more than two years.
  • additional Bactericides are dispensed with, particularly since 2-phenoxyalkanols 2-phenoxyethanol, has bacteriostatic properties and thus the required microbiological stabilization causes or at least with the microbiological Stabilization contributes.
  • the present invention has for its object a Lubricant and preferably a cooling lubricant available to put up a high physical and microbiological Stability and where it is even under extreme Conditions does not lead to the formation of phenols.
  • the lubricant according to the invention comprises at least one additive for the physical and / or microbiological stabilization of the liquid or viscous composition, the additive being an aromatic alcohol of the formula I.
  • m is an integer between 0 and 4 and R 1 to R 5 is hydrogen, a linear or branched C 1 -C 4 alkyl group, but R 1 to R 5 are not simultaneously hydrogen.
  • the lubricant according to the invention has a number of advantages on. So it should first be noted that the invention Lubricant even under the extreme mentioned above Conditions, i.e. when anaerobic areas occur, Non-compliance with certain limit concentrations as well with high bacterial colonization, no phenol forms, which in turn it is explained that in the in the invention Lubricant does not contain any additive on the phenyl group Ether group is present. Also surprisingly found be that in lubricants, especially cooling lubricants or concentrates of cooling lubricants, by using the one described above and represented in formula I.
  • the additive according to formula I can easily be converted into lubricants, Cooling lubricant concentrates and cooling lubricants can be incorporated, in addition to those already listed above Advantages in this case the additive formulated herewith Lubricants according to the invention not only microbiologically but also physically stabilized. This is attributed to that the addition of the additive according to formula I the Solubility of other components in lubricants, Coolants and coolant concentrates included are improved, so that they are accordingly mentioned compositions by the presence of such Additives are particularly good physically and microbiologically are stabilized and therefore have a long shelf life exhibit.
  • Lubricants are within the scope of the present application lubricants that are miscible or immiscible with water understand that applied immediately without dilution with water become. Coolant concentrates can either directly or after adding water, the latter then referred to as water-mixed cooling lubricants are.
  • the invention Lubricant for mechanical processing or processing of materials used, the term material in particular materials made of metal, plastic, glass or ceramic, while the term processing or Processing includes all the steps involved in a Machining or non-cutting processing, for example with Drilling, cutting, grinding, milling, punching, turning, reaming, Thread forming and drilling, broaching or the like.
  • the lubricant according to the invention causes a Cooling and / or lubrication is brought about, so that in particular wear of the tools is suppressed that at least protection against corrosion of the tool and / or workpiece is temporary and that metal dust and chips are removed become.
  • Lubricant emulsions which are preferred to lubricants, cooling lubricant concentrates or Cooling lubricant is used
  • additive according to formula I with other additives based on alkyl glycols, especially ethylene glycol, Propylene glycol, butylene glycol, pentylene glycol, hexylene glycol, Diethylene glycol and / or triethylene glycol, in corresponding Lubricants, coolant concentrates and / or coolants is used, which in the invention
  • Additive containing lubricant is equally well tolerated with such other additives based on monoalkyl ethers, for example methyl diglycol, ethyl diglycol, Propyl diglycol, butyl diglycol and / or derivatives or oligomers of propylene glycol and / or glycerol are.
  • Lubricant contained additive with many different built additives is compatible and hereby partially even has a synergistic effect, however surprisingly in a variety of application cases shown that the sole presence of the additive according to formula I above the lubricant provided with it, in particular the cooling lubricant or Coolant concentrate, an excellent physical and gives microbiological stability, as follows is still documented in the specific exemplary embodiments. Therefore, a particularly suitable embodiment of the Lubricant according to the invention the additive according to formula I. as the only additive to physical and microbiological Stabilization of the lubricant.
  • the additive contained in the lubricant according to the invention preferably has a structure as represented below by the formula II.
  • R 3 , R 4 , R 5 represent a hydrogen and / or a linear or branched C 1 -C 4 alkyl group, but at the same time not all hydrogen and o an integer between 0 and 4.
  • the substituent R 5 which is in particular a linear C 1 -C 4 alkyl group, occupies an ortho or para position in the formulas I and II.
  • Lubricant have the following listed as an additive concrete connections on:
  • additives which are chemically known as a C 1 -C 4 alkyl-2-phenyl-1-ethanol 1-phenyl-1-ethanol, a C 1 -C 4 alkyl-1-phenyl-1-ethanol, a 1-phenyl-1-propanol, a C 1 -C 4 alkyl-1-phenyl-1-propanol , a 2-phenyl-2-propanol, a C 1 -C 4 alkyl-2-phenyl-2-propanol, a C 1 -C 4 alkyl-3-phenyl-1-propanol, a 1-phenyl-1 -butanol, a C 1 -C 4 alkyl-1-phenyl-1-butanol, a 4-phenyl-2-butanol, a
  • the concentration preferably varies of the additive according to formula I or the above specifically mentioned type in the liquid or viscous invention Lubricant composition between 0.5% by weight and 20% by weight, in particular between 3% by weight and 18% by weight, each based on the ready-to-use lubricant composition.
  • Lubricant especially the coolant concentrate or the coolant already mixed with water
  • the chemical composition of that contained varies Emulsifier.
  • a non-ionic and / or anionic emulsifier the lubricant according to the invention or added to the cooling lubricant concentrate according to the invention, the corresponding cooling lubricant mixed with water then such an anionic and / or nonionic Has emulsifier.
  • the cooling lubricant concentrate according to the invention or the cooling lubricant already mixed with water are alkoxylated, especially ethoxylated Fatty alcohols, alkoxylated, especially ethoxylated fatty acids and / or alkoxylated, especially ethoxylated, alkyl aryl compounds and / or alkoxylated, especially ethoxylated, To view alkyl / aryl phosphoric acid esters.
  • Preferred anionic emulsifiers are such emulsifiers based on an alkali soap, an alkanolamine soap, a petroleum sulfonate, a sulfated fatty acid ester and / or an alkanolamine.
  • Concrete emulsifiers in particular those present in the lubricant, cooling lubricant or cooling lubricant concentrate according to the invention, are the C 16 -C 18 fatty alcohols or C 16 -C 18 fatty acids, which are in particular ethoxylated with 2 to 10 moles of ethylene oxide.
  • Castor oil ethoxylates which are ethoxylated with 2 to 10 mol of ethylene oxide, alkylphenol ethoxylates which are ethoxylated with 2 to 10 mol of ethylene oxide, C 18 -C 22 potassium carboxylates, ammonium carboxylates with monoethanolamine, triethanolamine, aminobutanol or monoisopropanolamine, sodium alkylbenzenesulfates with a molecular weight between 350 and 500, and tall oil fatty acid monoethanolamide are highly compatible with the previously described embodiments of the additive according to the invention, so that these specific emulsifiers are particularly preferably present in the lubricant according to the invention.
  • concentration of the emulsifier in the Lubricant is present, it should be noted that this concentration is between 0.5% by weight and 50% by weight, in particular between 3% and 30% by weight, based on the ready-to-use Lubricant varies.
  • Lubricant also has at least one Corrosion protection component.
  • This is in particular for alkali soap, alkanolamine soap, petroleum sulfonates, Alkanolamides, alkoxylated alkyl / aryl phosphoric acid esters, organic boron compounds, alkali or ammonium salts of amidocarboxylic acids, thiophosphoric acid esters and Salts, alkyl succinic acid derivatives and / or alkyl imidazoles.
  • the lubricant according to the invention as a corrosion protection component is a potassium carboxylate, preferably of a C 7 -C 12 and / or a C 18 -C 22 carboxylic acid, an ammonium carboxylate, in particular the aforementioned carboxylic acids, a sodium alkylbenzenesulfonate, preferably with a molecular weight between 350 and 500, a tall oil fatty acid monoethanolamide, an ammonium borate with monoethanolamine, triethanolamine, aminobutanol and / or monoisopropanolamine, a sulfonamidocarboxylic acid, a dialkyldithiophosphate, preferably a C 3 -C 8 dialkyldithiophosphate, a succinic acid derivative or calcium and / or heterocyclic nitrogen compounds, heterocyclic nitrogen compounds Having sulfonates, such an embodiment of the lubricant according to the invention has a high effectiveness in relation to the corrosion protection required in the mechanical processing
  • the concentration of the corrosion protection component preferably varies in the ready-to-use lubricant between 3 % By weight and 50% by weight, preferably between 5% by weight and 30 % By weight.
  • Additives, emulsifiers and corrosion protection components other embodiments of the preferred lubricant according to the invention, in which the Lubricant according to the invention further additives in a concentration between 0.2% by weight and 30% by weight, in each case related on the ready-to-use lubricant formulation.
  • These other additives are in particular: such additives that the lubricant at a high application pressure protect and / or wear the mechanical Prevent tools used in metalworking.
  • EP / AW additives fatty acid esters, especially native, synthetic and / or sulfurized native or synthetic esters, sulfurized hydrocarbons, sulfurized fatty acid esters, chlorinated paraffins, Phosphorus derivatives, sulfur-phosphorus derivatives, thiophosphoric acid esters and their salts, polyalkylene glycol and / or fatty amides to call.
  • fungicides Bactericides, defoamers, antioxidants, non-ferrous metal deactivators, Solubilizers, anti-fog additives and / or Odor improvers may be included, but in particular regarding the concentration of fungicides and bactericides It should be noted that these products are partially or completely by the additive according to the invention described at the beginning can be replaced.
  • boric acid and its salts Isothiazolinones, sodium pyrion, siloxane defoamers, ditert.butyl-hydroxytoluene, Benzotriazole, ethylhexanediol, polypropylene glycols, Polymethacrylates, phosphonates and / or usual To name fragrances.
  • Lubricant has a basic connection
  • this basic connection can be structured differently.
  • the lubricant according to the invention as Basic compound water as well as the additive according to of the formulas I and II or those specifically mentioned above Type, wherein at least one corrosion protection component may still be present can be included.
  • Lubricants in the lubricant according to the invention as a basic compound at least one mineral oil, at least one Fatty acid esters, at least one glycol, at least one polyglycol and / or contain at least one fatty alcohol, wherein especially naphthenic mineral oils, paraffin-based mineral oils, aromatic mineral oils, white oils, Poly [ ⁇ ] olefins, sulfurized hydrocarbons, chlorinated paraffins, native esters, preferably vegetable and / or animal triglycerides, synthetic fatty acid esters, in particular Mono- and / or dicarboxylic acid esters, synthetic polycarboxylic acid esters, synthetic polyester, synthetic Kornplexester and / or synthetic triglycerides, preferably medium chain triglycerides, sulfurized native and / or synthetic Contain esters.
  • rapeseed oil modified rape oil, castor oil, castor oil derivatives, trimethylolpropanoic acid ester, Ethylene glycols, propylene glycols, polyethylene glycol, Amine ethoxylates and / or polyamine ethoxylates.
  • the polyethylene glycols include, in particular, polyethylene glycol, preferably with an ethylene oxide / propylene oxide ratio of 1/0 and a molecular weight of 200 ⁇ 20, polyethylene glycol 600 with an ethylene oxide / propylene oxide ratio of 1/0 and a molecular weight of 600 ⁇ 60 as well as a Polyethylene glycol, which is sold under the trade name B11 / 300 is available and an ethylene oxide / propylene oxide ratio of 1/1 and has a molecular weight of 300 ⁇ 40 call.
  • Preferred fatty alcohols are cetyl alcohol, oleyl alcohol and Guebert alcohols ( ⁇ '-branched alcohols), where especially oleyl alcohol with an iodine value between 90 and 95 as the base compound of the lubricant according to the invention gives excellent properties.
  • the lubricant according to the invention has at least one mineral oil as the base compound, it is particularly advantageous if this mineral oil has a viscosity between 2 and 1,500 mm 2 / s and a density between 800 kg / m 3 and 950 kg / m 3 , the viscosity values at 40 ° C and the density values at 15 ° C.
  • Lubricant in which at least one as a basic connection Mineral oil is present it is also recommended that you do so a mineral oil is selected whose aromatic content less than 10% by weight, the content of polycyclic aromatics less than 3% by weight and its concentration Benz [a] pyrene is less than 3 ppm.
  • the lubricant according to the invention contains at least one of the aforementioned native and / or synthetic fatty acid esters as the base compound, the viscosity of the fatty acid ester advantageously varies between 20 mm 2 / s and 100 mm 2 / s, while the neutralization number is in particular less than 15, the Viscosity values can be measured at 40 ° C.
  • Such embodiments of the lubricant according to the invention which as a base compound at least one glycol and / or contain at least one polyglycol, preferably have such Products based on the molecular weight of the glycol or polyglycol varies between 60 and 30,000.
  • a fatty alcohol is found to be special advantageously shown that the relevant fatty alcohol Has an iodine number between 40 and 130.
  • a lubricant which is a miscible with water or mixed cooling lubricant
  • Cooling lubricant then those listed above Basic compounds as droplets with a size smaller than 100 nm, in particular with a size between 90 nm and 35 nm.
  • Such a water miscible or mixed cooling lubricant can also be called a microemulsion become.
  • the additive according to the formulas I and II as well as the specific type mentioned above preferably in amine-free lubricants, amine-free Coolant concentrates and / or amine-free coolants is used.
  • the present invention further relates to an additive for the physical and / or microbiological stabilization of a lubricant, in particular a cooling lubricant concentrate or a cooling lubricant, of the type described above.
  • the additive according to the invention which is an aromatic alcohol, has a composition as described in detail above and is subsequently represented by the formula I.
  • R 1 to R 5 are hydrogen, a linear and / or branched C 1 -C 4 alkyl group and m is an integer between 0 and 4, but R 1 to R 5 is not simultaneously hydrogen.
  • the additive according to the invention has all the advantages, such as they above in connection with the invention Lubricant are described so that to avoid repetition reference is made to the above statements, which also apply analogously to the additive according to the invention.
  • the additive according to the invention does not form any phenols, if within the lubricant with a high bacterial population anaerobic conditions prevail and when concentration of the previously described and in formulas I and II reproduced additive according to the invention in the lubricant falls below a predetermined limit.
  • Lubricant has been exposed, that in the presence of the additive according to the invention in Lubricant for the addition of bactericides and / or fungicides can largely be dispensed with that the invention Lubricant at least with regard to the additive is very readily biodegradable without the biological Degradation phenols are formed and that come in all of the usual Lubricants that shown in formulas I and II additive according to the invention can be incorporated without problems, without segregation occurring.
  • the lubricant mixed with the additive according to the invention of such lubricants in which this invention Additive is not present in particular also differs in that the added with the additive according to the invention Lubricant an even and constant distribution of droplets of the base compound, making the superior Lubricating effect of the additive according to the invention offset lubricant compared to conventional Lubricants in mechanical processing or processing of materials, in particular materials made of metal, Plastic, glass or ceramics.
  • This Advantage is also particularly evident when the lubricant mixed with the additive according to the invention Cooling lubricant or a cooling lubricant concentrate is, wherein such a coolant concentrate is then preferred mixed with water to form the cooling lubricant becomes.
  • the additive according to the invention preferably has such a structure as is represented by structural formula II.
  • R 3 , R 4 , R 5 represent a hydrogen and / or a linear or branched C 1 -C 4 alkyl group, but at the same time not all hydrogen and o an integer between 0 and 4.
  • the additive according to the invention is a C 1 -C 4 alkyl-2-phenyl-1-ethanol, a 1-phenyl-1-ethanol, a C 1 -C 4 alkyl-1-phenyl-1- ethanol, a 1-phenyl-1-propanol, a C 1 -C 4 alkyl-1-phenyl-1-propanol, a 2-phenyl-2-propanol, a C 1 -C 4 alkyl-2-phenyl- 2-propanol, a C 1 -C 4 alkyl-3-phenyl-1-propanol, a 1-phenyl-1-butanol, a C 1 -C 4 alkyl-1-phenyl-1-butanol, a 4- Phenyl-2-butanol, a C 1 -C 4 alkyl-4-phenyl-2-butanol, a 2-phenyl-2-butanol, a C 1 -C 4 alkyl-2-ethanol,
  • the cooling lubricants contained 1 - 3 as an additive for microbiological and physical stabilization 4- (ethylphenyl) -benzyl alcohol in three different concentrations, which are given in Table 1 above.
  • the cooling lubricants contained 4 to 6 as an additive for microbiological and physical stabilization 2- (o-methylphenyl) -ethanol in three different concentrations, which are given in Table 2 above.
  • the cooling lubricants contained 7 to 9 as an additive for microbiological and physical stabilization 1-phenyl-1-propanol in three different concentrations, which are given in Table 3 above.
  • the cooling lubricants contained 10 to 12 as an additive for microbiological and physical stabilization 1-phenyl-2-propanol in three different concentrations, which are given in Table 4 above.
  • the composition of the cooling lubricants 25 - 33 is shown in Tables 9 a to 9 c below.
  • cooling lubricants 1 - 33 For the cooling lubricants 1 - 33 mentioned above note that for the production of these cooling lubricants the same mineral oils, fatty acid esters, fatty alcohol ethoxylates, Petroleum sulfonates, aliphatic fatty acids, KOH 45, defoamers and nonferrous metal inhibitors were used, wherein only in the examples 1 - 24 the concentration and the chemical structure of the respective additive, which, however, is always a phenyl alcohol of the above acted specifically, distinguished, while in the embodiments 25-33 this additive by the conventional additive phenoxyethanol, 2,2-dimethyl-3-phenyl-1-propanol and by the linear alcohols 3-phenyl-1-propanol and 4-phenyl-1-butanol was replaced or none Additive contained.
  • the standard emulsion For the test series to check the antimicrobial effectiveness, 95 g of a 2%, highly contaminated standard emulsion were mixed with 5 g of the cooling lubricant concentrates 1 - 33 in question, the standard emulsion having a total bacterial count of at least 10 7 colony-forming units / ml, determined by means of the aforementioned Dipslides at an incubation time of 24 h and 30 ° C. Furthermore, the standard emulsion contained the maximum amount of fungi and yeasts detectable with these dip slides. The ATP content of the standard emulsion corresponded to 2,300,000 RLE (relative light units).
  • the lubricant according to embodiment 35 contained as Additive 1-phenyl-1-propanol, while in the embodiment 37 was included as an additive 1-phenyl-2-propanol.
  • the respective lubricant was used immediately after manufacture visually assessed. It should be noted that the lubricants at a lubricant temperature of 50 ° C 34 and 36 showed phase separation while the lubricants 35 and 37 formed a homogeneous, clear liquid.
  • the lubricants were at a lubricant temperature of 20 ° C 34 and 36 cloudy, while lubricants 35 and 37 remained clear.
  • the lubricants were at a lubricant temperature of 0 ° C 34 and 36 still cloudy while the lubricants 35 and 37 remained clear.
  • the lubricant according to embodiment 39 contained as Additive 1-phenyl-1-propanol, while in the embodiment 41 was included as an additive 1-phenyl-2-propanol.
  • the respective lubricant was used immediately after manufacture visually assessed. It should be noted that the lubricants at a lubricant temperature of 50 ° C 38 and 40 showed a phase separation while the lubricants 39 and 41 formed a homogeneous, clear liquid.
  • the lubricants were at a lubricant temperature of 20 ° C 38 and 40 cloudy, while the lubricants 39 and 41 remained clear.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
EP98122266A 1997-11-26 1998-11-24 Lubrifiant d'usinage mécanique de matériaux et additif pour lubrifiant Withdrawn EP0919607A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19752370 1997-11-26
DE19752370 1997-11-26

Publications (2)

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EP0919607A2 true EP0919607A2 (fr) 1999-06-02
EP0919607A3 EP0919607A3 (fr) 2000-08-09

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0976493A3 (fr) * 1998-07-24 2002-12-18 Rhenus Lub GmbH & Co. KG Procédé de refroidissement et/ou de lubrification

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Publication number Priority date Publication date Assignee Title
DE102011077654B4 (de) * 2011-06-16 2020-12-03 BSH Hausgeräte GmbH Verfahren zur Herstellung eines Blechteils durch Umformen
CN110747688B (zh) * 2019-10-14 2023-03-24 浙江理工大学 矿物油类的造纸烘缸用乳液剥离剂组合物及其制备方法

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Publication number Priority date Publication date Assignee Title
DE1642026B2 (de) * 1967-08-03 1978-08-24 Bayer Ag, 5090 Leverkusen Mikrobizide Mittel
DE2020349A1 (de) * 1970-04-25 1971-11-11 Goldschmidt Ag Th Biocide Zubereitung
OA03896A (fr) * 1970-11-20 1975-08-14 Lilly Co Eli Procédé de préparation d'hydrocarbures aralkyliques.
DE2405004C3 (de) * 1974-02-02 1979-11-29 Haarmann & Reimer Gmbh, 3450 Holzminden Desodorierende Mittel
US4446161A (en) * 1982-03-29 1984-05-01 General Foods Corporation Aromatic, monohydric alcohols as preservatives for foods
US4770670A (en) * 1986-12-22 1988-09-13 Arco Chemical Company Fire resistant microemulsions containing phenyl alcohols as cosurfactants
IT1223113B (it) * 1987-11-13 1990-09-12 Ross Sergio Del Fluidi acquosi per lavorazioni meccaniche
DE4217690C1 (en) * 1992-05-25 1993-09-23 Schuelke & Mayr Gmbh, 2000 Norderstedt, De Disinfectant for use in animal stalls - contains aldehyde(s), alkyl:alkanol(s) and phenoxy:alkanol(s)
DE4447361A1 (de) * 1994-12-21 1996-06-27 Schuelke & Mayr Gmbh Biozide Alkohole, ihre Herstellung und ihre Verwendung

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0976493A3 (fr) * 1998-07-24 2002-12-18 Rhenus Lub GmbH & Co. KG Procédé de refroidissement et/ou de lubrification

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EP0919607A3 (fr) 2000-08-09

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