EP0629235A1 - Surface-active base for non-soap lubricants. - Google Patents

Surface-active base for non-soap lubricants.

Info

Publication number
EP0629235A1
EP0629235A1 EP93904004A EP93904004A EP0629235A1 EP 0629235 A1 EP0629235 A1 EP 0629235A1 EP 93904004 A EP93904004 A EP 93904004A EP 93904004 A EP93904004 A EP 93904004A EP 0629235 A1 EP0629235 A1 EP 0629235A1
Authority
EP
European Patent Office
Prior art keywords
radical
carbon atoms
alkyl radical
alkyl
lubricant according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP93904004A
Other languages
German (de)
French (fr)
Other versions
EP0629235B1 (en
Inventor
Alfred Laufenberg
Birgit Winkelmann
Werner Strothoff
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.)
Ecolab GmbH and Co oHG
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP0629235A1 publication Critical patent/EP0629235A1/en
Application granted granted Critical
Publication of EP0629235B1 publication Critical patent/EP0629235B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • 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
    • 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
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino 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
    • 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
    • C10M133/30Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms containing a nitrogen-to-oxygen bond
    • 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
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/40Polysaccharides, e.g. cellulose
    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/12Polysaccharides, e.g. cellulose, biopolymers
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/20Containing nitrogen-to-oxygen bonds
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/20Containing nitrogen-to-oxygen bonds
    • C10M2215/204Containing nitrogen-to-oxygen bonds containing nitroso groups
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • 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
    • 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
    • C10N2040/30Refrigerators lubricants or compressors lubricants
    • 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
    • C10N2040/32Wires, ropes or cables lubricants
    • 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
    • C10N2040/34Lubricating-sealants
    • 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
    • C10N2040/36Release agents or mold release agents
    • 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
    • C10N2040/38Conveyors or chain belts
    • 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
    • C10N2040/40Generators or electric motors in oil or gas winning field
    • 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
    • C10N2040/42Flashing oils or marking oils
    • 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
    • C10N2040/44Super vacuum or supercritical use
    • 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
    • C10N2040/50Medical uses
    • 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 new surfactant base for soap-free lubricants known per se, containing alkylamines and / or amphoteric compounds, optionally water and further additives and / or auxiliaries.
  • the invention further relates to the use of the lubricant as a chain lubricant in the food industry.
  • the lubricants according to the invention are used here for the lubrication, cleaning and disinfection of automatic chain and belt lubrication systems which, when filling foodstuffs, preferably beverages, in glass and plastic bottles, cans, glasses, barrels, beverage containers (KEG), paper containers and cardboard containers and the like are used.
  • the chain lubricants previously used as lubricants are based, on the one hand, on fatty acids in the form of their water-soluble alkali or alkanolamine salts or on fatty amines in the form of their organic or inorganic salts.
  • DE-A-23 13 330 describes soap-based lubricants which contain aqueous mixtures of cis-cig fatty acid salts and surface-active substances.
  • DE-A-36 31 953 describes a method for lubricating chain-shaped bottle conveyor belts in beverage removal plants, in particular in breweries, and for cleaning the belts by means of a liquid cleaning agent, which is characterized in that the chain-shaped bottle conveyor belts are lubricated with belt lubricants based on neutralized primary fatty amines, which preferably have 12 to 18 C atoms and contain an unsaturated fraction of more than 10%, and the bottle conveyor ⁇ tapes with cationic cleaning agents, namely quaternary ammonium compounds such as alkyltrimethylammon um-, dialkyldimethylammonium and alkyldimethylbenzylammonium chlorides or organic acids.
  • quaternary ammonium compounds such as alkyltrimethylammon um-, dialkyldimethylammonium and alkyldimethylbenzylammonium chlorides or organic acids.
  • DE-A-38 31 448 relates to aqueous, clear water-soluble, soap-free lubricant preparations, a process for their preparation and the use of the lubricant preparations according to the invention, in particular as lubricants for the transport of glass bottles or polyethylene terephthalate bottles.
  • the essentially neutral aqueous lubricant preparations (pH in the range from 6 to 8) contain alkylbenzenesulfonates, alkoxylated Al anolphosphate and alkane carboxylic acids, optionally in addition to conventional solubilizers, solvents, defoamers and disinfectants.
  • DE-A-39 05 548 describes lubricants which contain at least one secondary and / or tertiary amine and / or salts of such amines.
  • PET polyethylene terephthalate
  • PET reusable bottles have proven particularly useful in this area for carbonated beverages such as mineral water and lemonades.
  • chain conveyor belt lubricants A more or less large part of the chain conveyor belt lubricant remains on the bottles, dries and sometimes damages these bottles.
  • cracks in the PET material so-called stress cracks, have been found in application technology. In extreme cases, this leads to the bottle bursting.
  • the object of the present invention was therefore to provide a chain conveyor belt lubricant which meets the needs of the application side in that the So-called coefficient of friction is equal to or less than 0.1 to 0.12, the product simultaneously cleans, lubricates and disinfects, the product can be used in the lowest possible concentrations, the product does not damage the PET bottles, the product can be used regardless of the water hardness and the product is particularly suitable for mixed PET glass.
  • the object of the present invention was achieved by the use of certain nonionic surfactants which fulfill all the requirements for chain conveyor belt lubricants, as listed above.
  • the present invention relates to soap-free lubricants based on amphoteric compounds, primary, secondary and / or tertiary amines and / or salts of such amines of the general formula (I), (Ila), (Ilb), (Illa), (Illb ), (Illb), (IIIc), (IVa) and (IVb)
  • R is a saturated or mono- or polyunsaturated, linear or branched alkyl radical having 6 to 22 carbon atoms, which may be replaced by -OH, -NH 2 , -NH-, -C0-, - (CH CH 0) ⁇ - or - (CH 2 CH 2 CH 2 0)] - may be substituted,
  • Rl for hydrogen, an alkyl radical with 1 to 4 carbon atoms, a hydroxyalkyl radical with 1 to 4 carbon atoms or a radical -R ⁇ COOM
  • R2 only in the case where M represents a negative charge for hydrogen, an alkyl radical with 1 to 4 C atoms, or a hydroxyalkyl radical with 1 to 4 C atoms
  • - or - (CH 2 CH CH 2 0) ⁇ - may be substituted,
  • R 4 is a substituted or unsubstituted, linear or branched, saturated or mono- or polyunsaturated alkyl radical having 6 to 22 carbon atoms, the substituents being at least one amine, I in, hydroxy, halogen and / or carboxy residue, a substituted or unsubstituted phenyl residue which has at least one amine, imine, hydroxy, halogen, carboxy and / or a linear or branched, saturated or mono- or polyunsaturated substituent May have an alkyl radical having 6 to 22 carbon atoms,
  • R5 for hydrogen or - independently of R 4 - for a radical R 4 ,
  • X stands for an anion from the group amidosulfonate, nitrate, halide, sulfate, hydrogen carbonate, carbonate, phosphate or R ⁇ -COO", where
  • R6 represents hydrogen, a substituted or unsubstituted, linear or branched alkyl radical having 1 to 20 C atoms or alkenyl radical having 2 to 20 C atoms, which may have at least one hydroxyl, amine or imine radical as substituents, or a substituted one or unsubstituted phenyl radical, which may have an alkyl radical with 1 to 20 C atoms as a substituent, and
  • R? and R8 in each case independently of one another for a substituted or unsubstituted, linear or branched alkyl radical having 1 to 20 C atoms or alkenyl radical having 2 to 20 C atoms, which may have at least one hydroxyl, amine or imine radical as a substituent, or a substituted or unsubstituted phenyl radical, which may have an alkyl radical with 1 to 20 C atoms as a substituent, M for hydrogen, alkali metal, ammonium, an alkyl radical with 1 to 4 carbon atoms, a benzyl radical or a negative charge, n for an integer in the range from 1 to 12, m for an integer in the range from 0 to 5 and
  • 1 represents a number in the range from 0 to 5
  • alkyldimethylamine oxides containing alkyldimethylamine oxides and / or alkyl oligoglycosides as nonionic surfactants.
  • R saturated or mono- or polyunsaturated, linear alkyl radical with 10 to 18 C atoms, which can optionally be substituted by -C0-, in particular unsubstituted, saturated linear alkyl radical with 12 to 14 C atoms,
  • R 1 hydrogen, alkyl radical with 1 to 3 carbon atoms or a radical
  • R2 hydrogen or alkyl radical with 1 to 3 carbon atoms
  • R 3 methylene or dimethylene residue, in particular methylene residue
  • M hydrogen or a negative charge
  • the lubricant combinations according to the invention show a very good coefficient of friction, a low foaming behavior, a good cleaning effect and good skin tolerance.
  • Moderate foaming behavior improves the lubricating effect in problem areas, such as Turntables, changers, etc., high substantivity and thus high lubricating performance even under unfavorable operating conditions (eg belt lubrication), generally usable even with equipment shortcomings, good cleaning effect, high capillary activity and film formation on surfaces, even in the presence of organic loads and acids or alkalis effective and also non-corrosive as a concentrate.
  • the lubricant combinations according to the invention are both independent of the water quality and also low-foaming, stable in storage at low temperatures, not corrosive and particularly gentle on the environment and skin.
  • the compounds of the general formula (I) are known in principle, as is the process for their preparation from "fatty amines and secondary products", company lettering from Hoechst AG.
  • the lubricants according to the invention contain the compounds of the general formulas (I) to (IV) in amounts of 1 to 99% by weight, preferably in amounts of 5 to 15% by weight, based on the overall formulation. Accordingly, such lubricant combinations in the sense of the invention can consist exclusively of the amphoteric compounds mentioned and the associated surfactant base. Furthermore, the invention also includes lubricant formulations which contain only a minor proportion of the compounds of the general formulas (I) to (IV), preferably in amounts of 5 to 15% by weight and in particular 10 to 12 % By weight. In this case, the rest of the lubricant formulations preferably consist of water and additionally, if appropriate, of additives and / or auxiliaries and the surfactant base mentioned.
  • Suitable as lubricant components are primary, secondary and / or tertiary amines and / or salts of such amines, as described, among other things, in the German patent application DE-A-3905 548 cited above.
  • the lubricants according to the invention can be primary or secondary amines of the general formulas (Ila) or (Ilb)
  • Di-coco-amine, di-stearyl-amine, di-tallow-amine and corresponding salts preferably the acetates.
  • the lubricants according to the invention can be secondary diamines of the general formulas (purple), (Illb) or (IIIc)
  • N-lauryl-propylenediamine and N-tallow-propylenediamine each in the form of the free amines and in the form of the acetate salts.
  • the lubricants according to the invention can contain tertiary amines of the general formulas (IVa) or (IVb)
  • radicals R 4 and X ⁇ each have the meanings given for the general formulas (Ila) and (Ilb) and the radicals R ⁇ and each independently mean: a substituted or unsubstituted, linear or branched alkyl radical with 1 to 20 carbon atoms or alkenyl radical with 2 to 20 carbon atoms, which as a substituent at least one
  • Substituents can have an alkyl radical with 1 to 20 carbon atoms.
  • tertiary amines of the general formulas (IVa) and (IVb) are: N, N-dipropyl-N-laurylamine, N, N-dimethyl-N-laurylamine, N, N-dimethyl-N-hexadecylamine, N, N-dimethyl-N-cocosamine, N, N-dimethyl-N-cetylamine and the corresponding acetate salts.
  • Primary, secondary and tertiary amines which correspond to the general formulas (II), (III) and (IV) given above can be prepared by processes known from the literature and some are offered as commercial products, for example from Hoechst AG, Frankfurt am Main, Germany, under the name GENAMIN R or from Lonza AG, Basel, Switzerland, under the name L0NZABAC R 12.
  • the weight ratio of the compounds of the general formula (I) to the amines of the general formulas (II), (III) and / or (IV) is not critical. However, a weight ratio of compounds of the general formula (I) to the compounds of the general formulas (II), (III) and / or (IV) in the range from 10: 1 to 1:10, in particular a ratio of 5: 1, is preferred up to 1: 1.
  • the weight ratio mentioned above is based on the sum of the compounds (II), (III) and (IV) which may be used individually.
  • the lubricants according to the invention can contain, as auxiliaries, solubilizers for obtaining a homogeneous, clear water-soluble application solution.
  • solubilizers for obtaining a homogeneous, clear water-soluble application solution.
  • examples of these are: alcohols, polyalcohols, ethers or polyethers, in particular isopropanol, butylglycol, butyl diglycol or ethylene glycol ether.
  • the amount of the solubilizer to be used depends in each case on the betaine or amine used, the person skilled in the art will determine the required amount of solubilizer by trial and error in the individual case. In general, additions to solubilizers in the range from 1 to 20% by weight, based on the overall formulation, are sufficient.
  • the alkyldimetylamine oxides to be used are equipped with a chain length of 10 to 18, in particular 12 to 14, carbon atoms in the alkyl radical.
  • the alkyl chains can be linear or branched, saturated, mono- or polyunsaturated.
  • Alkyl oligoglycosides for the purposes of the present invention preferably comprise compounds of the formula (V), Rl-0- [G] p (V)
  • R 1 represents an alkyl radical with 4 to 22 carbon atoms
  • [G] stands for a sugar residue with 5 or 6 carbon atoms and p stands for numbers from 1 to 10.
  • Alkyl oligoglycosides are preferred which are derived from aldoses or ketoes and, because of their ready availability, in particular from glucose.
  • the preferred alkyl oligoglycosides are thus the alkyl oligoglucosides.
  • the alkyl radical R 1 can be derived from primary alcohols having 4 to 22, preferably 8 to 16, in particular 8 to 10, carbon atoms. Typical examples are butanol, capro alcohol, caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, behenyl alcohol and their technical mixtures based on natural fats and oils, for example palm oil, palm kernel oil, coconut oil or beef tallow.
  • Alkyl oligoglycosides are known substances which can be obtained by the relevant methods of preparative organic chemistry.
  • EP-A-0301298 As representative of the extensive literature regarding its structure and synthesis, reference is made to the European patent application EP-A-0301298.
  • the surfactants mentioned in the range from 1 to 10% by weight, based on the total formulation, are sufficient for wetting the chains and plate conveyor belts.
  • the amine oxides as well as the alkyl oligoglycosides can each be used alone or in a mixture.
  • auxiliaries from the prior art are, for example, alkoxylated fatty amines, fatty alcohols or alkoxylated fatty alcohols.
  • these surfactants have the disadvantage of increased stress corrosion cracking in PET bottles. Therefore, such surfactants are preferably not used in the sense of the present invention. If, however, this is desired, their share should be kept as low as possible.
  • the lubricants according to the invention preferably have a pH in the range from 4 to 11, in particular in the range from 6 to 9. If the pH of the lubricant is not already in this range, it can be added by adding an acid, preferably one Acid with the anion X "defined above, for example with acetic acid to the desired value.
  • the lubricants have a dynamic viscosity of less than 300 mPa.s, in particular less than 150 Pa.s and particularly preferably in the range from 5 to 100 mPa.s - each at 20 ° C.
  • a separate adjustment of the viscosity to the values mentioned is generally not necessary or is optionally carried out by adding suitable amounts of the preferred diluent water or a solubilizer.
  • the lubricants according to the invention can be prepared by simply mixing the components with water, optionally with the addition of the additives and / or auxiliaries mentioned.
  • the present invention relates to the use of lubricants of the type described above as chain lubricants in the food industry, in particular for automatic chain and belt lubrication systems.
  • the lubricants according to the invention are generally diluted with water.
  • Such aqueous application solutions generally contain 0.01% by weight of compounds of the general formulas (I) to (IV), preferably 0.01 to 0.2% by weight and in particular 0.02 to 0.04% by weight. % of such compounds and 0.1 to 1% by weight of the surfactants according to the invention mentioned.
  • the products according to the invention do not cause stress corrosion cracking and can therefore be used without problems for PET and PC containers.
  • PET polyethylene terephthalate
  • PC polycarbonate
  • Neutral pH values are particularly preferred for clear water-soluble concentrates.
  • the lubricants according to the invention are namely suitable in the concentration required for chain and belt lubrication also for cleaning empties as well as machines and machine parts.
  • central foam systems in the food industry are partially equipped with permanently installed, automatic systems which, after the production process or during breaks, automatically clean the outside of fillers, cylindroconical fermentation and storage tanks, conveyor belts and other machines and systems .
  • the lubricants according to the invention can be used with great advantage.
  • the present invention thus also relates to the use of lubricants of the type described above for disinfecting and cleaning empties, machines and systems in the food and beverage industry.
  • the PET bottles are filled with carbonated water of 4.5 vol% CO 2 and sealed accordingly.
  • the bottles are immersed in the substance to be tested in the bottom area (see Table 1) and stored at 38 ° C for 72 hours. The bottle is then sampled (from no stress cracks to the destroyed bottle).
  • Bottle transport speed approx. 1 m / s
  • Spraying the bottle conveyor belt with 0.4% band lubricant solution as mentioned in the examples. Spraying performance of the nozzles: 4 1 / h, 1 nozzle per belt.
  • the coefficient of friction " ⁇ " given below is the quotient of the measured tensile stress for a bottle to the weight of the bottle in grams. Furthermore, the products were tested with hard water (16 ° d) according to the provisions of DIN 53902.
  • the foam behavior is assessed according to the following classes:
  • the coefficient of friction should be 0.10 to 0.12 or less. If the value exceeds 0.15, the lubricating effect and thus the problem-free transport clearly deteriorates.
  • the clear water solubility of the application solutions should also be guaranteed over a longer test period in order to avoid deposits in ball valve filters, nozzles, spray and distribution systems, belts and transport goods.
  • the foam development should be low, since excessive foam not only interferes with the workflow (automatic bottle inspector) and occupational safety (risk of slipping), but also can soften the label and penetrate into the not yet sealed container. In addition, the coefficient of friction deteriorates due to excessive foaming tendency.
  • Anionic surfactants such as alkylbenzenesulfonate cannot be incorporated into the cationically reacting chain lubricants based on alkylamines, so that only amine oxides and alkyl polyglucosides remain for use in corresponding chain lubricants.
  • PET suitability: few cracks. Clear water solubility: opaque
  • PET suitability: no cracks. Clear water solubility: slightly opaque

Abstract

PCT No. PCT/EP93/00413 Sec. 371 Date Nov. 9, 1994 Sec. 102(e) Date Nov. 9, 1994 PCT Filed Feb. 22, 1993 PCT Pub. No. WO93/18121 PCT Pub. Date Sep. 16, 1993Soapless lubricant compositions, especially for use in the food and beverage industry, comprising an amphoteric compound, a tertiary amine and/or a salt thereof, and a nonionic surfactant which is one or more of an alkyl dimethylamine oxide or an alkyl oligoglycoside.

Description

Tensidbasis für seifenfreie Schmiermittel Surfactant base for soap-free lubricants
Die vorliegende Erfindung betrifft eine neue Tensidbasis für an sich bekannte seifenfreie Schmiermittel, enthaltend Alkylamine und/oder amphotere Verbindungen, gegebenenfalls Wasser sowie weitere Zusatz- und/oder Hilfsstoffe.The present invention relates to a new surfactant base for soap-free lubricants known per se, containing alkylamines and / or amphoteric compounds, optionally water and further additives and / or auxiliaries.
Die Erfindung betrifft weiterhin die Verwendung der Schmiermittel als Kettenschmiermittel in der Lebensmittelindustrie. Insbesondere finden die erfindungsgemäßen Schmiermittel hier Verwendung zum Schmieren, Reinigen und Desinfizieren von automatischen Ketten- und Bandschmieranlagen, die beim Abfüllen von Lebensmitteln, vorzugs¬ weise Getränken, in Glas- und Kunststoffflaschen, Dosen, Gläser, Fässer, Getränkecontainer (KEG), Papier- und Pappbehälter und der¬ gleichen eingesetzt werden.The invention further relates to the use of the lubricant as a chain lubricant in the food industry. In particular, the lubricants according to the invention are used here for the lubrication, cleaning and disinfection of automatic chain and belt lubrication systems which, when filling foodstuffs, preferably beverages, in glass and plastic bottles, cans, glasses, barrels, beverage containers (KEG), paper containers and cardboard containers and the like are used.
Die bisher als Schmiermittel eingesetzten Kettengleitmittel basie¬ ren einerseits auf Fettsäuren in Form ihrer wasserlöslichen Alkali¬ oder Alkanolaminsalze oder auf Fettaminen in Form ihrer organischen oder anorganischen Salze.The chain lubricants previously used as lubricants are based, on the one hand, on fatty acids in the form of their water-soluble alkali or alkanolamine salts or on fatty amines in the form of their organic or inorganic salts.
Die DE-A-23 13 330 beschreibt Schmiermittel auf Seifenbasis, die wäßrige Mischungen von Cis-Cig-Fettsäuresalzen und oberflächenakti¬ ven Substanzen enthalten.DE-A-23 13 330 describes soap-based lubricants which contain aqueous mixtures of cis-cig fatty acid salts and surface-active substances.
Neben diesen Schmiermitteln auf Seifenbasis werden ansonsten haupt¬ sächlich solche auf Basis von primären Fettaminen verwendet. So be¬ schreibt die DE-A-36 31 953 ein Verfahren zum Schmieren von ket¬ tenförmigen Flaschentransportbändern in Getränkeabfü11betrieben, insbesondere in Brauereien, sowie zum Reinigen der Bänder mittels eines flüssigen Reinigungsmittels, das dadurch gekennzeichnet ist, daß man die kettenförmigen Flaschentransportbänder mit Bandschmier¬ mitteln auf Basis neutralisierter primärer Fettamine, die vorzugs¬ weise 12 bis 18 C-Atome aufweisen und einen ungesättigten Anteil von mehr als 10 % enthalten, schmiert und die Flaschentransport¬ bänder mit kationischen Reinigungsmitteln, nämlich quaternären Am¬ moniumverbindungen wie Alkyltrimethylammon um-, Dialkyldimethyl- ammonium- und Alkyldimethylbenzylammoniumchloriden oder organischen Säuren reinigt.In addition to these soap-based lubricants, those based on primary fatty amines are otherwise mainly used. For example, DE-A-36 31 953 describes a method for lubricating chain-shaped bottle conveyor belts in beverage removal plants, in particular in breweries, and for cleaning the belts by means of a liquid cleaning agent, which is characterized in that the chain-shaped bottle conveyor belts are lubricated with belt lubricants based on neutralized primary fatty amines, which preferably have 12 to 18 C atoms and contain an unsaturated fraction of more than 10%, and the bottle conveyor ¬ tapes with cationic cleaning agents, namely quaternary ammonium compounds such as alkyltrimethylammon um-, dialkyldimethylammonium and alkyldimethylbenzylammonium chlorides or organic acids.
Schließlich sind im Stand der Technik weitere Kettenschmiermittel bekannt; so beschreibt die EP-A-0 044458 Schmiermittelzubereitun¬ gen, die praktisch frei von Fettsäureseifen sind und die weiterhin ein carboxyliertes nichtionisches Tensid und ein Acylsarcosinat enthalten. Der pH-Wert dieser Produkte beträgt 7 bis 11 und liegt somit vorzugsweise im neutralen bis alkalischen Bereich.Finally, further chain lubricants are known in the prior art; thus describes EP-A-0 044458 lubricant preparations which are practically free of fatty acid soaps and which further contain a carboxylated nonionic surfactant and an acyl sarcosinate. The pH of these products is 7 to 11 and is therefore preferably in the neutral to alkaline range.
Die DE-A-38 31 448 betrifft schließlich wäßrige, klarwasserlös¬ liche, seifenfreie SchmiermittelZubereitungen, ein Verfahren zu ihrer Herstellung und die Verwendung der erfindungsgemäßen Schmier¬ mittelzubereitungen, insbesondere als Schmiermittel zum Transport von Glasflaschen oder Polyethylenterephthalat-Flaschen. Die im we¬ sentlichen neutralen wäßrigen SchmiermittelZubereitungen (pH im Bereich von 6 bis 8) enthalten Alkylbenzolsulfonate, alkoxylierte AI anolphosphate und Alkancarbonsäuren, gegebenenfalls neben üb¬ lichen Lösungsvermittlern, Lösungsmitteln, Entschäumungsmitteln und Desinfektionsmitteln.Finally, DE-A-38 31 448 relates to aqueous, clear water-soluble, soap-free lubricant preparations, a process for their preparation and the use of the lubricant preparations according to the invention, in particular as lubricants for the transport of glass bottles or polyethylene terephthalate bottles. The essentially neutral aqueous lubricant preparations (pH in the range from 6 to 8) contain alkylbenzenesulfonates, alkoxylated Al anolphosphate and alkane carboxylic acids, optionally in addition to conventional solubilizers, solvents, defoamers and disinfectants.
Allerdings zeigen auch diese beiden oben beschriebenen Produkte noch folgende drei Nachteile:However, these two products described above also have the following three disadvantages:
1. Sie sind mikrobiologisch ungünstig, da sie hervorragende Wachs¬ tumsbedingungen für Mikroorganismen schaffen. 2. Weiterhin zeigen sie nur eine geringe Reinigungskraft.1. They are microbiologically unfavorable because they create excellent growth conditions for microorganisms. 2. Furthermore, they show only a low cleaning power.
3. Schließlich weisen sie ein schwer zu kontroll erendes Schaum¬ verhalten auf.3. Finally, they have a foam behavior that is difficult to control.
In der DE-A-39 05 548 werden Schmiermittel beschrieben, die min¬ destens ein sekundäres und/oder tertiäres Amin und/oder Salze der¬ artiger Amine enthalten.DE-A-39 05 548 describes lubricants which contain at least one secondary and / or tertiary amine and / or salts of such amines.
In jüngster Zeit werden häufig Getränke in Polyethylenterephthalat (PET)-Flaschen abgefüllt. Insbesondere für kohlensäurehaltige Ge¬ tränke wie Mineralwasser und Limonaden haben sich in diesem Bereich PET-Mehrwegflaschen bewährt. Während des Transportes der Flaschen in den Abfüllbetrieben kommen diese Flaschen mit Kettentransport¬ band-Schmiermitteln in Kontakt. Ein mehr oder weniger großer Teil des Kettentransportband-Schmiermittels verbleibt an den Flaschen, trocknet an und führt teilweise zu Schädigungen dieser Flaschen. Insbesondere sind in der Anwendungstechnik Risse im PET-Material, sogenannte Spannungsrisse, festgestellt worden. Dies führt im Ex¬ tremfall zum Platzen der Flasche.Recently, beverages have often been filled into polyethylene terephthalate (PET) bottles. PET reusable bottles have proven particularly useful in this area for carbonated beverages such as mineral water and lemonades. During the transport of the bottles in the bottling plants, these bottles come into contact with chain conveyor belt lubricants. A more or less large part of the chain conveyor belt lubricant remains on the bottles, dries and sometimes damages these bottles. In particular, cracks in the PET material, so-called stress cracks, have been found in application technology. In extreme cases, this leads to the bottle bursting.
Aus diesem Grunde wurden bisher zur Schmierung der Flaschen prak¬ tisch ausschließlich seifenhaltige Kettentransport-Schmiermittel eingesetzt, die von den Herstellern jeweils auf ihre spezielle Eig¬ nung untersucht und freigegeben wurden. Allgemein im Stand der Technik bekannte Kettentransportband-Schmiermittel auf Alkylamin- basis, die wie oben aufgeführt, eine breite Verwendung im Stand der Technik für den Transport von anderen Getränkegebinden finden, führten scheinbar zu einer Schädigung der Flaschen.For this reason, so far only soap-containing chain transport lubricants have been used for lubricating the bottles, which have been examined and approved by the manufacturers for their particular suitability. Chain conveyor belt lubricants based on alkylamine, which are generally known in the prior art and, as listed above, are widely used in the prior art for the transport of other beverage containers, apparently caused damage to the bottles.
Die Aufgabe der vorliegenden Erfindung bestand somit darin, ein Kettentransportband-Schmiermittel zur Verfügung zu stellen, das den Bedürfnissen der Anwendungsseite dahingehend gerecht wird, daß der sogenannte Reibbeiwert gleich oder weniger 0,1 bis 0,12 beträgt, das Produkt gleichzeitig reinigt, schmiert und desinfiziert, das Produkt in möglichst geringen Konzentrationen einsetzbar ist, das Produkt die PET-Flaschen nicht schädigt, das Produkt unabhängig von der Wasserhärte einsetzbar ist und das Produkt insbesondere für den Mischbetrieb PET-Glas geeignet ist.The object of the present invention was therefore to provide a chain conveyor belt lubricant which meets the needs of the application side in that the So-called coefficient of friction is equal to or less than 0.1 to 0.12, the product simultaneously cleans, lubricates and disinfects, the product can be used in the lowest possible concentrations, the product does not damage the PET bottles, the product can be used regardless of the water hardness and the product is particularly suitable for mixed PET glass.
Überraschenderweise wurde gefunden, daß nicht die Alkylamine selbst, sondern die üblicherweise eingesetzten Hilfsstoffe wie nichtionische Tenside, insbesondere alkoxilierte Fettamine, Fett¬ alkohole, alkoxilierte Fettalkohole, zu einer mehr oder weniger großen Schädigung der PET-Mehrwegflaschen führten.Surprisingly, it was found that not the alkylamines themselves, but rather the auxiliaries usually used, such as nonionic surfactants, in particular alkoxylated fatty amines, fatty alcohols, alkoxylated fatty alcohols, led to more or less serious damage to the returnable PET bottles.
Die Aufgabe der vorliegenden Erfindung wurde gelöst durch die Ver¬ wendung bestimmter nichtionogener Tenside, die sämtliche Anforde¬ rungen an Kettentransportband-Schmiermittel, wie oben aufgeführt, erfüllen.The object of the present invention was achieved by the use of certain nonionic surfactants which fulfill all the requirements for chain conveyor belt lubricants, as listed above.
Die vorliegende Erfindung betrifft seifenfreie Schmiermittel auf der Basis von amphoteren Verbindungen, primären, sekundären und/oder tertiären Aminen und/oder Salzen derartiger Amine der all¬ gemeinen Formel (I), (Ila), (Ilb), (Illa), (Illb), (Illb), (IIIc), (IVa) und (IVb) The present invention relates to soap-free lubricants based on amphoteric compounds, primary, secondary and / or tertiary amines and / or salts of such amines of the general formula (I), (Ila), (Ilb), (Illa), (Illb ), (Illb), (IIIc), (IVa) and (IVb)
RlRl
R-[NH-(CH2)n]m - R3 - COOM (I)R- [NH- (CH 2 ) n ] m - R 3 - COOM (I)
R -NH-R5 (Ha)R -NH-R5 (Ha)
4.N+H2-R5 x- (Hb)4. N + H 2 -R5 x- (Hb)
R4-NH-(CH2)3NH2 (lila)R 4 -NH- (CH 2 ) 3NH 2 (purple)
R4-NH-(CH2)3N+H3 x- (πib)R4-NH- (CH 2 ) 3 N + H 3 x- (πib)
R4-N+H2-(CH2)3-N+H32X" (IIIc)R 4 -N + H 2 - (CH 2 ) 3-N + H 3 2X "(IIIc)
R4-NR7R8 (IVa) und/oderR 4 -NR7R8 (IVa) and / or
R4-N+HR7R8 x- (IVb)R 4 -N + HR7R8 x- (IVb)
wobeiin which
R für einen gesättigten oder einfach oder mehrfach ungesättigten, linearen oder verzweigten Alkylrest mit 6 bis 22 C-Atomen, der gegebenenfalls durch -OH, -NH2, -NH-, -C0-, -(CH CH 0)ι- oder -(CH2CH2CH20)]- substituiert sein kann,R is a saturated or mono- or polyunsaturated, linear or branched alkyl radical having 6 to 22 carbon atoms, which may be replaced by -OH, -NH 2 , -NH-, -C0-, - (CH CH 0) ι- or - (CH 2 CH 2 CH 2 0)] - may be substituted,
Rl für Wasserstoff, einen Alkylrest mit 1 bis 4 C-Atomen, einen Hydroxyalkylrest mit 1 bis 4 C-Atomen oder einen Rest -R^COOMRl for hydrogen, an alkyl radical with 1 to 4 carbon atoms, a hydroxyalkyl radical with 1 to 4 carbon atoms or a radical -R ^ COOM
R2 nur für den Fall, daß M eine negative Ladung darstellt für Was¬ serstoff, einen Alkylrest mit 1 bis 4 C-Atomen, oder einen Hy¬ droxyalkylrest mit 1 bis 4 C-Atomen, R3 fQr einen gesättigten oder einfach oder mehrfach ungesättigten, linearen oder verzweigten Alkylrest mit 1 bis 12 C-Atomen, der gegebenenfalls durch -OH, -NH2, -NH-, -C0-, -(CH2CH20)-|- oder -(CH2CH CH20)ι- substituiert sein kann,R2 only in the case where M represents a negative charge for hydrogen, an alkyl radical with 1 to 4 C atoms, or a hydroxyalkyl radical with 1 to 4 C atoms, R3 for a saturated or mono- or polyunsaturated, linear or branched alkyl radical having 1 to 12 carbon atoms, which may be replaced by -OH, -NH 2 , -NH-, -C0-, - (CH 2 CH 2 0) - | - or - (CH 2 CH CH 2 0) ι- may be substituted,
R4 für einen substituierten oder unsubstituierten, linearen oder verzweigten, gesättigten oder einfach oder mehrfach ungesättig¬ ten Alkylrest mit 6 bis 22 C-Atomen, der als Substituenten min¬ destens einen Amin-, I in-, Hydroxy-, Halogen- und/oder Car- boxyrest aufweisen kann, einen substituierten oder unsubstituierten Phenylrest, der als Substituenten mindestens einen Amin-, Imin-, Hydroxy-, Halo¬ gen-, Carboxy- und/oder einen linearen oder verzweigten, ge¬ sättigten oder einfach oder mehrfach ungesättigten Alkylrest mit 6 bis 22 C-Atomen aufweisen kann,R 4 is a substituted or unsubstituted, linear or branched, saturated or mono- or polyunsaturated alkyl radical having 6 to 22 carbon atoms, the substituents being at least one amine, I in, hydroxy, halogen and / or carboxy residue, a substituted or unsubstituted phenyl residue which has at least one amine, imine, hydroxy, halogen, carboxy and / or a linear or branched, saturated or mono- or polyunsaturated substituent May have an alkyl radical having 6 to 22 carbon atoms,
R5 für Wasserstoff oder - unabhängig von R4 - für einen Rest R4,R5 for hydrogen or - independently of R 4 - for a radical R 4 ,
X" für ein Anion aus der Gruppe Amidosulfonat, Nitrat, Halogenid, Sulfat, Hydrogencarbona , Carbonat, Phosphat oder R^-COO" steht, wobeiX "stands for an anion from the group amidosulfonate, nitrate, halide, sulfate, hydrogen carbonate, carbonate, phosphate or R ^ -COO", where
R6 für Wasserstoff, einen substituierten oder unsubstituierten, linearen oder verzweigten Alkylrest mit 1 bis 20 C-Atomen oder Alkenylrest mit 2 bis 20 C-Atomen, die als Substituenten min¬ destens einen Hydroxy-, Amin- oder Iminrest aufweisen können, oder einen substituierten oder unsubstituierten Phenylrest, der als Substituenten einen Alkylrest mit 1 bis 20 C-Atomen auf¬ weisen kann, steht, undR6 represents hydrogen, a substituted or unsubstituted, linear or branched alkyl radical having 1 to 20 C atoms or alkenyl radical having 2 to 20 C atoms, which may have at least one hydroxyl, amine or imine radical as substituents, or a substituted one or unsubstituted phenyl radical, which may have an alkyl radical with 1 to 20 C atoms as a substituent, and
R? und R8 jeweils unabhängig voneinander für einen substituierten oder unsubstituierten, linearen oder verzweigten Alkylrest mit 1 bis 20 C-Atomen oder Alkenylrest mit 2 bis 20 C-Atomen, die als Substituenten mindestens einen Hydroxy-, Amin- oder Imin¬ rest aufweisen können, oder einen substituierten oder unsubsti¬ tuierten Phenylrest, der als Substituenten einen Alkylrest mit 1 bis 20 C-Atomen aufweisen kann, M für Wasserstoff, Alkalimetall, Ammonium, einen Alkylrest mit 1 bis 4 C-Atomen, einen Benzylrest oder eine negative Ladung, n für eine ganze Zahl im Bereich von 1 bis 12, m für eine ganze Zahl im Bereich von 0 bis 5 undR? and R8 in each case independently of one another for a substituted or unsubstituted, linear or branched alkyl radical having 1 to 20 C atoms or alkenyl radical having 2 to 20 C atoms, which may have at least one hydroxyl, amine or imine radical as a substituent, or a substituted or unsubstituted phenyl radical, which may have an alkyl radical with 1 to 20 C atoms as a substituent, M for hydrogen, alkali metal, ammonium, an alkyl radical with 1 to 4 carbon atoms, a benzyl radical or a negative charge, n for an integer in the range from 1 to 12, m for an integer in the range from 0 to 5 and
1 für eine Zahl im Bereich von 0 bis 5 steht,1 represents a number in the range from 0 to 5,
enthaltend Alkyldimethylaminoxide und/oder Alkyloligoglycoside als nichtionische Tenside.containing alkyldimethylamine oxides and / or alkyl oligoglycosides as nonionic surfactants.
Im Sinne der vorliegenden Erfindung sind solche Verbindungen der allgemeinen Formel (I) bevorzugt, für welche gilt:For the purposes of the present invention, preference is given to those compounds of the general formula (I) for which:
R = gesättigter oder einfach oder mehrfach ungesättigter, linearer Alkylrest mit 10 bis 18 C-Atomen, der gegebenenfalls durch -C0- substituiert sein kann, insbesondere unsubstituierter, gesättigter linearer Alkylrest mit 12 bis 14 C-Atomen,R = saturated or mono- or polyunsaturated, linear alkyl radical with 10 to 18 C atoms, which can optionally be substituted by -C0-, in particular unsubstituted, saturated linear alkyl radical with 12 to 14 C atoms,
R1 = Wasserstoff, Alkylrest mit 1 bis 3 C-Atomen oder ein RestR 1 = hydrogen, alkyl radical with 1 to 3 carbon atoms or a radical
-CH CH20H, insbesondere Wasserstoff oder Alkylrest mit 1 bis 3 C-Atomen,-CH CH 2 0H, in particular hydrogen or alkyl radical with 1 to 3 carbon atoms,
R2 = Wasserstoff oder Alkylrest mit 1 bis 3 C-Atomen,R2 = hydrogen or alkyl radical with 1 to 3 carbon atoms,
R3 = Methylen- oder Di-methylen-rest, insbesondere Methylenrest,R 3 = methylene or dimethylene residue, in particular methylene residue,
M = Wasserstoff oder eine negative Ladung, n = 2 oder 3, insbesondere 2 = 0, 1 oder 2, insbesondere 0.M = hydrogen or a negative charge, n = 2 or 3, in particular 2 = 0, 1 or 2, in particular 0.
Hinsichtlich ihrer Anwendungseigenschaften zeigen die erfindungs¬ gemäßen Schmiermittelkombinationen einen sehr guten Reibbeiwert, ein geringes Schaumverhalten, eine gute Reinigungswirkung sowie gute Hautverträglichkeit. Zusätzlich zu den genannten positiven Eigenschaften werden folgende Randbedingungen erfüllt: Mäßiges Schaumverhalten verbessert die Schmierwirkung an Problemzonen, wie Drehtellern, Wechslern usw., hohe Substantivität und damit hohe Schmierleistung auch bei ungünstigen Betriebsbedingungen (z.B. Un¬ terbandschmierung), allgemein einsetzbar auch bei apparativen Unzu¬ länglichkeiten, guter Reinigungseffekt, hohe Kapillaraktivität und Filmbildung an Oberflächen, auch in Gegenwart von organischen Be¬ lastungen und Säuren oder Alkalien wirksam und auch als Konzentrat nicht korrosiv.With regard to their application properties, the lubricant combinations according to the invention show a very good coefficient of friction, a low foaming behavior, a good cleaning effect and good skin tolerance. In addition to the positive properties mentioned, the following boundary conditions are met: Moderate foaming behavior improves the lubricating effect in problem areas, such as Turntables, changers, etc., high substantivity and thus high lubricating performance even under unfavorable operating conditions (eg belt lubrication), generally usable even with equipment shortcomings, good cleaning effect, high capillary activity and film formation on surfaces, even in the presence of organic loads and acids or alkalis effective and also non-corrosive as a concentrate.
Die erfindungsgemäßen Schmiermittelkombinationen sind beim Einsatz in der Getränkeindustrie im Gegensatz zu den bislang eingesetzten Kettenschmiermitteln sowohl unabhängig von der Wasserqualität als auch schaumarm, lagerstabil bei tiefen Temperaturen, nicht korrosiv und besonders umweit- und hautvertäglich.When used in the beverage industry, the lubricant combinations according to the invention, in contrast to the chain lubricants used hitherto, are both independent of the water quality and also low-foaming, stable in storage at low temperatures, not corrosive and particularly gentle on the environment and skin.
Die Verbindungen der allgemeinen Formel (I) sind prinzipiell ebenso wie das Verfahren zu ihrer Herstellung aus "Fettamine und Folge¬ produkte", Firmenschrift der Hoechst AG, bekannt.The compounds of the general formula (I) are known in principle, as is the process for their preparation from "fatty amines and secondary products", company lettering from Hoechst AG.
Beispiele für amphotere Verbindungen der allgemeinen Formel (I), die im Sinne der Erfindung auch bevorzugt eingesetzt werden, sind nachstehend genannt: Dodecyl-aminopropyl-glycin, Dodecyl-di(amino- ethyl)-glycin, N-Dodecyl-N,N-dipropyl-glycin, N-Cocos-N,N-dimethyl- glycin (Cocos = Fettalkylreste mit vorzugsweise 12 bzw. 14 C-Ato¬ men), N-Hexadecyl-N.N-dimethyl-glycin, N-Soja-N,N-dimethyl-glycin (Soja = ein- und zweifach ungesättigte Fettalkylreste mit vorzugs¬ weise 18 C-Atomen), N-Decyl-N,N-dimethylglycin, Dodecyl-di(amino- propyl)-glycin, Cio.ig-Fettsäureamidoethyl-N-hydroxyethyl-glycin.Examples of amphoteric compounds of the general formula (I) which are also preferably used in the context of the invention are mentioned below: dodecylaminopropylglycine, dodecyldi (aminoethyl) glycine, N-dodecyl-N, N- dipropyl-glycine, N-coco-N, N-dimethyl-glycine (coco = fatty alkyl residues with preferably 12 or 14 C-atoms), N-hexadecyl-NN-dimethyl-glycine, N-soybean-N, N- dimethyl-glycine (soy = mono- and di-unsaturated fatty alkyl residues with preferably 18 carbon atoms), N-decyl-N, N-dimethylglycine, dodecyl-di (aminopropyl) -glycine, Cio.ig fatty acid amidoethyl-N -hydroxyethyl-glycine.
Die erfindungsgemäßen Schmiermittel enthalten die Verbindungen der allgemeinen Formeln (I) bis (IV) in Mengen von 1 bis 99 Gew.-%, vorzugsweise in Mengen von 5 bis 15 Gew-%, bezogen auf die Gesamt¬ formulierung. Mithin können derartige Schmiermittelkombinationen im Sinne der Erfindung ausschließlich aus den genannten amphoteren Verbindungen bestehen und der dazugehörigen Tensidbasis. Ferner umfaßt die Er¬ findung auch solche Schmiermittel-Formulierungen, die die Verbin¬ dungen der allgemeinen Formeln (I) bis (IV) nur zu einem geringeren Anteil, vorzugsweise in Mengen von 5 bis 15 Gew.-% und insbesondere von 10 bis 12 Gew.-%, enthalten. Der Rest der Schmiermittel-Formu¬ lierungen besteht in diesem Falle vorzugsweise aus Wasser und zu¬ sätzlich gegebenenfalls aus Zusatz- und/oder Hilfsstoffen sowie der genannten Tensidbasis.The lubricants according to the invention contain the compounds of the general formulas (I) to (IV) in amounts of 1 to 99% by weight, preferably in amounts of 5 to 15% by weight, based on the overall formulation. Accordingly, such lubricant combinations in the sense of the invention can consist exclusively of the amphoteric compounds mentioned and the associated surfactant base. Furthermore, the invention also includes lubricant formulations which contain only a minor proportion of the compounds of the general formulas (I) to (IV), preferably in amounts of 5 to 15% by weight and in particular 10 to 12 % By weight. In this case, the rest of the lubricant formulations preferably consist of water and additionally, if appropriate, of additives and / or auxiliaries and the surfactant base mentioned.
Als Schmiermittelbestandteile kommen ferner primäre, sekundäre und/oder tertiäre Amine und/oder Salze derartiger Amine in Be¬ tracht, wie sie - unter anderem - in der vorstehend zitierten deutschen Patentanmeldung DE-A-3905 548 beschrieben sind.Also suitable as lubricant components are primary, secondary and / or tertiary amines and / or salts of such amines, as described, among other things, in the German patent application DE-A-3905 548 cited above.
Somit können die erfindungsgemäßen Schmiermittel primäre oder se¬ kundäre Amine der allgemeinen Formeln (Ila) oder (Ilb)Thus, the lubricants according to the invention can be primary or secondary amines of the general formulas (Ila) or (Ilb)
R4-NH-R5 (Ila)R 4 -NH-R 5 (Ila)
R4-N+H2-R5 X- (Ilb)R 4 -N + H 2 -R5 X- (Ilb)
enthalten, wobei der Rest R4 bedeutet: einen substituierten oder unsubstituierten, linearen oder ver¬ zweigten, gesättigten oder einfach oder mehrfach ungesättigten Alkylrest mit 6 bis 22 C-Atomen, der als Substituenten minde¬ stens einen Amin-, Imin-, Hydroxy-, Halogen- und/oder Carboxy- rest aufweisen kann, einen substituierten oder unsubstituierten Phenylrest, der als Substituenten mindestens einen Amin-, Imin-, Hydroxy-, Halo- gen-, Carboxy- und/oder einen linearen oder verzweigten, ge¬ sättigten oder einfach oder mehrfach ungesättigten Alkylrest mit 6 bis 22 C-Atomen aufweisen kann, und X" für ein Anion aus der Gruppe Amidosulfonat, Nitrat, Halo¬ genid, Sulfat, Hydrogencarbonat, Carbonat, Phosphat oder R6-C00-, mit R6 = Wasserstoff, einen gesättigten, einfach oder mehrfach ungesättigten, linearen oder verzweigten, gegebenenfalls durch -0Hf -NH oder -NH- substituierten Alkylrest mit 1 bis 20 C-Atomen oder einen entsprechenden Alkenylrest mit 2 bis 20 C-Ato¬ men oder einen substituierten oder unsubstituierten Phenylrest, der als Substituenten einen Alkylrest mit 1 bis 20 C-Atomen aufweisen kann, steht und R5 für einen Rest R4 oder Wasserstoff.contain, where the radical R 4 means: a substituted or unsubstituted, linear or branched, saturated or mono- or polyunsaturated alkyl radical having 6 to 22 carbon atoms, the substituents being at least one amine, imine, hydroxy , Halogen and / or carboxy radical, a substituted or unsubstituted phenyl radical which has at least one amine, imine, hydroxyl, halo can have gene, carboxy and / or a linear or branched, saturated or mono- or polyunsaturated alkyl radical having 6 to 22 carbon atoms, and X "for an anion from the group amidosulfonate, nitrate, halogenide, sulfate , Bicarbonate, carbonate, phosphate or R6-C00-, with R6 = hydrogen, a saturated, mono- or polyunsaturated, linear or branched, optionally substituted by -0H f -NH or -NH- alkyl radical with 1 to 20 carbon atoms or a corresponding alkenyl radical with 2 to 20 carbon atoms or a substituted or unsubstituted phenyl radical, which may have an alkyl radical with 1 to 20 carbon atoms as substituents, and R5 represents a radical R 4 or hydrogen.
Als Beispiele für sekundäre Amine der allgemeinen Formel (Ila) und (Ilb) seien genannt:Examples of secondary amines of the general formulas (Ila) and (Ilb) are:
Di-cocos-amin, Di-stearyl-amin, Di-talg-amin sowie entsprechende Salze, vorzugsweise die Acetate.Di-coco-amine, di-stearyl-amine, di-tallow-amine and corresponding salts, preferably the acetates.
Die erfindungsgemäßen Schmiermittel können sekundäre Diamine der allgemeinen Formeln (lila), (Illb) oder (IIIc)The lubricants according to the invention can be secondary diamines of the general formulas (purple), (Illb) or (IIIc)
R -NH-(CH2)3NH2 (lila)R -NH- (CH 2 ) 3 NH 2 (purple)
R4-NH-(CH2)3N+H3 x- (τIIb) R 4 -NH- (CH 2 ) 3 N + H 3 x- (τ IIb)
R -N+H2-(CH2)3-N+H32X~ (IIIc)R -N + H 2 - (CH 2 ) 3 -N + H 3 2X ~ (IIIc)
enthalten, wobei die Reste R4 und X~ jeweils die vorstehend für die allgemeinen Formeln (Ila) und (Ilb) angegebenen Bedeutungen haben. Als Beispiele für sekundäre Diamine der allgemeinen Formeln (lila), (Illb) und (IIIc) seien genannt:contain, where the radicals R 4 and X ~ each have the meanings given above for the general formulas (Ila) and (Ilb). Examples of secondary diamines of the general formulas (purple), (Illb) and (IIIc) are:
N-Lauryl-propylendiamin und N-Talg-propylendiamin, jeweils in Form der freien Amine sowie in Form der Acetat-Salze.N-lauryl-propylenediamine and N-tallow-propylenediamine, each in the form of the free amines and in the form of the acetate salts.
Schließlich können die erfindungsgemäßen Schmiermittel tertiäre Amine der allgemeinen Formeln (IVa) oder (IVb)Finally, the lubricants according to the invention can contain tertiary amines of the general formulas (IVa) or (IVb)
R4-NR7R8 (ιva)R 4 -NR7R8 (ιva)
enthalten, wobei die Reste R4 und X~ jeweils die für die allgemei¬ nen Formeln (Ila) und (Ilb) angegebenen Bedeutungen haben und die Reste R^ und jeweils unabhängig voneinander bedeuten: einen substituierten oder unsubstituierten, linearen oder ver¬ zweigten Alkylrest mit 1 bis 20 C-Atomen oder Alkenylrest mit 2 bis 20 C-Atomen, die als Substituenten mindestens einencontain, where the radicals R 4 and X ~ each have the meanings given for the general formulas (Ila) and (Ilb) and the radicals R ^ and each independently mean: a substituted or unsubstituted, linear or branched alkyl radical with 1 to 20 carbon atoms or alkenyl radical with 2 to 20 carbon atoms, which as a substituent at least one
Hydroxy-, Amin- oder I inrest aufweisen können, oder einen substituierten oder unsubstituierten Phenylrest, der alsMay have hydroxyl, amine or I residue, or a substituted or unsubstituted phenyl residue, which as
Substituenten eine Alkylrest mit 1 bis 20 C-Atomen aufweisen kann.Substituents can have an alkyl radical with 1 to 20 carbon atoms.
Als Beispiele für tertiäre Amine der allgemeinen Formeln (IVa) und (IVb) seien genannt: N,N-Dipropyl-N-laurylamin, N,N-Dimethyl-N-lau- rylamin, N,N-Dimethyl-N-hexadecylamin, N,N-Dimethyl-N-cocosamin, N,N-Dimethyl-N-cetylamin sowie die entsprechenden Acetat-Salze.Examples of tertiary amines of the general formulas (IVa) and (IVb) are: N, N-dipropyl-N-laurylamine, N, N-dimethyl-N-laurylamine, N, N-dimethyl-N-hexadecylamine, N, N-dimethyl-N-cocosamine, N, N-dimethyl-N-cetylamine and the corresponding acetate salts.
Im Sinne der Erfindung ist es bevorzugt, zusätzlich zu den Verbin¬ dungen der allgemeinen Formel (I) Gemische von sekundären Diaminen der allgemeinen Formeln (III) und tertiären Aminen der allgemeinen Formeln (IV) einzusetzen, beispielsweise ein Gemisch aus N-Lauryl- propylen-diammoniumacetat und N,N-Dimethyl-N-lauryl-ammoniumacetat im Gewichsverhältnis 1 : 2 bis 3 : 1, vorzugsweise 2 : 1.For the purposes of the invention, it is preferred to use, in addition to the compounds of the general formula (I), mixtures of secondary diamines of the general formulas (III) and tertiary amines of the general formulas (IV), for example a mixture of N-lauryl propylene diammonium acetate and N, N-dimethyl-N-lauryl ammonium acetate in a weight ratio of 1: 2 to 3: 1, preferably 2: 1.
Primäre, sekundäre und tertiäre Amine, die den vorstehend angege¬ benen allgemeinen Formeln (II), (III) und (IV) entsprechen, können nach literaturbekannten Verfahren hergestellt werden und werden zum Teil als Handelsprodukte angeboten, beispielsweise von der Hoechst AG, Frankfurt am Main, Deutschland, unter der Bezeichnung GENAMINR oder von der Lonza AG, Basel, Schweiz, unter der Bezeichnung L0NZABACR 12.Primary, secondary and tertiary amines which correspond to the general formulas (II), (III) and (IV) given above can be prepared by processes known from the literature and some are offered as commercial products, for example from Hoechst AG, Frankfurt am Main, Germany, under the name GENAMIN R or from Lonza AG, Basel, Switzerland, under the name L0NZABAC R 12.
Das Gewichtsverhältnis der Verbindungen der allgemeinen Formel (I) zu den Aminen der allgemeinen Formeln (II), (III) und/oder (IV) ist nicht kritisch. Bevorzugt wird jedoch ein Gewichtsverhältnis von Verbindungen der allgemeinen Formel (I) zu den Verbindungen der allgemeinen Formeln (II), (III) und/oder (IV) im Bereich von 10 : 1 bis 1 : 10, insbesondere ein Verhältnis von 5 : 1 bis 1 : 1, einge¬ stellt. Das oben genannte Gewichtsverhältnis ist auf die Summe der gegebenenfalls einzeln eingesetzten Verbindungen (II), (III) und (IV) bezogen.The weight ratio of the compounds of the general formula (I) to the amines of the general formulas (II), (III) and / or (IV) is not critical. However, a weight ratio of compounds of the general formula (I) to the compounds of the general formulas (II), (III) and / or (IV) in the range from 10: 1 to 1:10, in particular a ratio of 5: 1, is preferred up to 1: 1. The weight ratio mentioned above is based on the sum of the compounds (II), (III) and (IV) which may be used individually.
Weiterhin können die erfindungsgemäßen Schmiermittel als Hilfs¬ stoffe Lösungsvermittler zum Erhalt einer homogenen, klarwasserlös¬ lichen Anwendungslösung enthalten. Als solche kommen beispielsweise in Betracht: Alkohole, Polyalkohole, Ether oder Polyether, insbe¬ sondere Isopropanol, Butylglykol, Butyldiglykol oder Ethylenglykol- ether. Die Menge des zu verwendenden Lösungsvermittlers richtet sich im Einzelfall nach dem eingesetzten Betain bzw. Amin, der Fachmann wird im Einzelfall die erforderliche Menge an Lösungsver¬ mittler durch Ausprobieren ermitteln. Im allgemeinen sind Zusätze an Lösungsvermittler im Bereich von 1 bis 20 Gew.-%, bezogen auf die Gesamtformulierung, hinreichend. In einer bevorzugten Ausführungsform der vorliegenden Erfindung sind die einzusetzenden Alkyldimetylaminoxide mit einer Kettenlänge von 10 bis 18, insbesondere 12 bis 14 C-Atomen, im Alkylrest ausge¬ stattet. Hierbei können die AIkylketten linear oder verzweigt, ge¬ sättigt, einfach oder mehrfach ungesättigt sein.Furthermore, the lubricants according to the invention can contain, as auxiliaries, solubilizers for obtaining a homogeneous, clear water-soluble application solution. Examples of these are: alcohols, polyalcohols, ethers or polyethers, in particular isopropanol, butylglycol, butyl diglycol or ethylene glycol ether. The amount of the solubilizer to be used depends in each case on the betaine or amine used, the person skilled in the art will determine the required amount of solubilizer by trial and error in the individual case. In general, additions to solubilizers in the range from 1 to 20% by weight, based on the overall formulation, are sufficient. In a preferred embodiment of the present invention, the alkyldimetylamine oxides to be used are equipped with a chain length of 10 to 18, in particular 12 to 14, carbon atoms in the alkyl radical. The alkyl chains can be linear or branched, saturated, mono- or polyunsaturated.
Alkyloligoglykoside im Sinne der vorliegenden Erfindung umfassen vorzugsweise Verbindungen der Formel (V), Rl-0-[G]p (V)Alkyl oligoglycosides for the purposes of the present invention preferably comprise compounds of the formula (V), Rl-0- [G] p (V)
in derin the
R1 für einen Alkylrest mit 4 bis 22 Kohlenstoffatomen,R 1 represents an alkyl radical with 4 to 22 carbon atoms,
[G] für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und p für Zahlen von 1 bis 10 steht.[G] stands for a sugar residue with 5 or 6 carbon atoms and p stands for numbers from 1 to 10.
Bevorzugt sind Alkyloligoglykoside, die sich von Aldosen bzw. Ke- tosen und wegen ihrer leichten Verfügbarkeit insbesondere von der Glucose ableiten. Die bevorzugten Alkyloligoglykoside sind somit die Alkyloligoglucoside.Alkyl oligoglycosides are preferred which are derived from aldoses or ketoes and, because of their ready availability, in particular from glucose. The preferred alkyl oligoglycosides are thus the alkyl oligoglucosides.
Die Indexzahl p in der allgemeinen Formel (V) gibt den Oligomeri¬ sierungsgrad (DP-Grad), d. h. die Verteilung von Mono- und Oligo- glykosiden an und steht für eine Zahl zwischen 1 und 10. Während p in einer gegebenen Verbindung stets ganzzahlig sein muß und hier vor allem die Werte p = 1 bis 6 annehmen kann, ist der Wert p für ein bestimmtes Alkyloligoglykosid eine analytisch ermittelte rech¬ nerische Größe, die meistens eine gebrochene Zahl darstellt. Be¬ vorzugt sind Alkyloligoglykoside mit einem mittleren Oligomerisie¬ rungsgrad p von 1,1 bis 3,0; besonders bevorzugt sind solche Alkyl¬ oligoglykoside, deren Oligomerisierungsgrad kleiner als 1,7 ist und insbesondere zwischen 1,2 und 1,4 liegt. Der Alkyrest R1 kann sich von primären Alkoholen mit 4 bis 22, vor¬ zugsweise 8 bis 16, insbesondere 8 bis 10, Kohlenstoffatomen ab¬ leiten. Typische Beispiele sind Butanol, Capronalkohol, Capryl- alkohol, Caprinalkohol, Laurylalkhohol, Myristylalkohol, Cetyl- alkohol, Stearylalkohol, Arachylalkohol, Behenylalkohol sowie deren technische Mischungen auf Basis von natürlichen Fetten und Ölen, beispielsweise Palmöl, Palmkernöl, Kokosöl oder Rindertalg.The index number p in the general formula (V) indicates the degree of oligomerization (DP degree), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10. While p in a given compound is always an integer must be and here can assume the values p = 1 to 6, the value p for a certain alkyl oligoglycoside is an analytically determined mathematical parameter, which usually represents a fractional number. Alkyl oligoglycosides with an average degree of oligomerization p of 1.1 to 3.0 are preferred; those alkyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4 are particularly preferred. The alkyl radical R 1 can be derived from primary alcohols having 4 to 22, preferably 8 to 16, in particular 8 to 10, carbon atoms. Typical examples are butanol, capro alcohol, caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, behenyl alcohol and their technical mixtures based on natural fats and oils, for example palm oil, palm kernel oil, coconut oil or beef tallow.
Alkyloligoglykoside stellen bekannte Stoffe dar, die nach den ein¬ schlägigen Methoden der präparativen organischen Chemie erhalten werden können. Stellvertretend für das umfangreiche Schrifttum hin¬ sichtlich ihrer Struktur und Synthese sei auf die Europäische Pa¬ tentanmeldung EP-A-0301298 verwiesen.Alkyl oligoglycosides are known substances which can be obtained by the relevant methods of preparative organic chemistry. As representative of the extensive literature regarding its structure and synthesis, reference is made to the European patent application EP-A-0301298.
Im allgemeinen sind die genannten Tenside im Bereich von 1 bis 10 Gew.%, bezogen auf die Gesamtformulierung für die Benetzung der Ketten und Plattentransportbänder ausreichend. Die Aminoxide ebenso wie die Alkyloligoglykoside können jeweils allein oder im Gemisch eingesetzt werden.In general, the surfactants mentioned in the range from 1 to 10% by weight, based on the total formulation, are sufficient for wetting the chains and plate conveyor belts. The amine oxides as well as the alkyl oligoglycosides can each be used alone or in a mixture.
Bekannte Hilfsstoffe des Standes der Technik sind beispielsweise alkoxylierte Fettamine, Fettalkohole oder alkoxylierte Fettalko¬ hole. Diese Tenside haben jedoch den Nachteil einer erhöhten Span- nungsrißkorrosionsbildung bei PET-Flaschen. Daher werden derartige Tenside im Sinne der vorliegenden Erfindung bevorzugt nicht einge¬ setzt. Sofern dies jedoch trotzdem erwünscht ist, so sollte jedoch ihr Anteil möglichst gering gehalten werden.Known auxiliaries from the prior art are, for example, alkoxylated fatty amines, fatty alcohols or alkoxylated fatty alcohols. However, these surfactants have the disadvantage of increased stress corrosion cracking in PET bottles. Therefore, such surfactants are preferably not used in the sense of the present invention. If, however, this is desired, their share should be kept as low as possible.
Die erfindungsgemäßen Schmiermittel weisen vorzugsweise einen pH- Wert im Bereich von 4 bis 11, insbesondere im Bereich von 6 bis 9, auf. Sofern der pH-Wert des Schmiermittels nicht bereits in diesem Bereich liegt, kann er durch Zugabe einer Säure, vorzugsweise einer Säure mit dem vorstehend definierten Anion X", beispielsweise mit Essigsäure auf den gewünschten Wert eingestellt werden.The lubricants according to the invention preferably have a pH in the range from 4 to 11, in particular in the range from 6 to 9. If the pH of the lubricant is not already in this range, it can be added by adding an acid, preferably one Acid with the anion X "defined above, for example with acetic acid to the desired value.
Im Hinblick auf eine optimale Dosiermöglichkeit ist es ferner von Vorteil, daß die Schmiermittel eine dynamische Viskosität von weni¬ ger als 300 mPa.s, insbesondere von weniger als 150 Pa.s und be¬ sonders bevorzugt im Bereich von 5 bis 100 mPa.s - jeweils bei 20 °C - aufweisen. Eine gesonderte Einstellung der Viskosität auf die genannten Werte ist im allgemeinen nicht erforderlich bzw. erfolgt gegebenenfalls durch Zusatz geeigneter Mengen des bevorzugten Ver¬ dünnungsmittels Wasser oder eines Lösungsvermittlers.With regard to an optimal dosing option, it is also advantageous that the lubricants have a dynamic viscosity of less than 300 mPa.s, in particular less than 150 Pa.s and particularly preferably in the range from 5 to 100 mPa.s - each at 20 ° C. A separate adjustment of the viscosity to the values mentioned is generally not necessary or is optionally carried out by adding suitable amounts of the preferred diluent water or a solubilizer.
Die erfindungsgemäßen Schmiermittel lassen sie sich durch einfaches Vermischen der Komponenten mit Wasser, gegebenenfalls unter Zusatz der genannten Zusatz- und/oder Hilfsstoffe, herstellen.The lubricants according to the invention can be prepared by simply mixing the components with water, optionally with the addition of the additives and / or auxiliaries mentioned.
Die vorliegende Erfindung betrifft schließlich die Verwendung von Schmiermitteln der vorstehend beschriebenen Art als Kettenschmier¬ mittel in der Lebensmittelindustrie, insbesondere für automatische Ketten- und Bandschmieranlagen. Für diesen Anwendungszweck werden die erfindungsgemäßen Schmiermittel im allgemeinen noch mit Wasser verdünnt. Derartige wäßrige Anwendungslösungen enthalten in der Regel 0,01 Gew.-% Verbindungen der allgemeinen Formeln (I) bis (IV), vorzugsweise 0,01 bis 0,2 Gew.-% und insbesondere 0,02 bis 0,04 Gew.-% derartiger Verbindungen, sowie 0,1 bis 1 Gew.-% der genannten, erfindungsgemäßen Tenside.Finally, the present invention relates to the use of lubricants of the type described above as chain lubricants in the food industry, in particular for automatic chain and belt lubrication systems. For this purpose, the lubricants according to the invention are generally diluted with water. Such aqueous application solutions generally contain 0.01% by weight of compounds of the general formulas (I) to (IV), preferably 0.01 to 0.2% by weight and in particular 0.02 to 0.04% by weight. % of such compounds and 0.1 to 1% by weight of the surfactants according to the invention mentioned.
Die erfindungsgemäßen Produkte verursachen im Gegensatz zu Stan¬ dard-Seifenprodukten keine Spannungsrißkorrosion und können daher für PET und PC-Gebinde problemlos eingesetzt werden. (PET = Poly- ethylenterephthalat, PC= Polycarbonat). Besonders bevorzugt für klarwasserlösliche Konzentrate sind neutrale pH-Werte. Die erfindungsgemäßen Schmiermittel eignen sich nämlich in der für die Ketten- und Bandschmierung erforderlichen Konzentration auch zum Reinigen von Leergut sowie Maschinen und Maschinenteilen.In contrast to standard soap products, the products according to the invention do not cause stress corrosion cracking and can therefore be used without problems for PET and PC containers. (PET = polyethylene terephthalate, PC = polycarbonate). Neutral pH values are particularly preferred for clear water-soluble concentrates. The lubricants according to the invention are namely suitable in the concentration required for chain and belt lubrication also for cleaning empties as well as machines and machine parts.
Ferner sind die zentralen Schaumsysteme in der Lebensmittelindu¬ strie teilweise mit fest installierten, automatischen Systemen aus¬ gestattet, die nach Produktionsablauf oder in Pausen automatisch die Außenreinigung von Füllern, zylindrokonisehen Gär- und Lager¬ tanks, Transportunterbändern und anderen Maschinen und Anlagen be¬ wirken.Furthermore, the central foam systems in the food industry are partially equipped with permanently installed, automatic systems which, after the production process or during breaks, automatically clean the outside of fillers, cylindroconical fermentation and storage tanks, conveyor belts and other machines and systems .
Auch hier können die erfindungsgemäßen Schmiermittel mit großem Vorteil Verwendung finden.Here too, the lubricants according to the invention can be used with great advantage.
Somit betrifft die vorliegende Erfindung ferner die Verwendung von Schmiermitteln der vorstehend beschriebenen Art zum Desinfizieren und Reinigen von Leergut, Maschinen und Anlagen in der Lebensmit¬ tel- und Getränkeindustrie. The present invention thus also relates to the use of lubricants of the type described above for disinfecting and cleaning empties, machines and systems in the food and beverage industry.
BeispieleExamples
Die vorliegende Erfindung wird durch die nachfolgenden Beispiele näher erläutert. In den erfindungsgemäßen Beispielen 1 und 2 werden der Reibungswiderstand und das Schaumverhalten von erfindungsgemä¬ ßen Schmiermittelformulierungen aufgezeigt. Zum Vergleich dienen die Vergleichsbeispiele 1 bis 3, die Produkte des Standes der Technik betreffen.The present invention is illustrated by the following examples. In examples 1 and 2 according to the invention, the frictional resistance and the foaming behavior of lubricant formulations according to the invention are shown. Comparative examples 1 to 3, which relate to products of the prior art, serve for comparison.
Alle Prozentangaben in den nachstehenden Formulierungs-Beispielen beziehen sich auf Gewichtsprozente.All percentages in the formulation examples below relate to percentages by weight.
Die PET-Flaschen werden mit kohlensäurehaltigem Wasser von 4,5 Vol% C02 gefüllt und entsprechend verschlossen. Die Flaschen werden im Bodenbereich in die zu prüfende Substan-z (siehe Tabelle 1) getaucht und bei 38° C für 72 Studen gelagert. Danach wird die Flasche bemu¬ stert (von keine Spannungsrisse bis zerstörte Flasche).The PET bottles are filled with carbonated water of 4.5 vol% CO 2 and sealed accordingly. The bottles are immersed in the substance to be tested in the bottom area (see Table 1) and stored at 38 ° C for 72 hours. The bottle is then sampled (from no stress cracks to the destroyed bottle).
Die Versuche zur Messung des Reibungswiderstandes, im folgenden kurz "Reibbeiwert" genannt, sind auf einem Techniku s-Flaschen- transportband unter folgenden Bedingungen durchgeführt worden:The tests for measuring the frictional resistance, hereinafter referred to as "coefficient of friction", were carried out on a Techniku s bottle conveyor under the following conditions:
Messung des Reibwiderstandes von 20 mit Wasser gefüllten 0,5 1 Euro-Bierflaschen als Zugspannung mit einem Dynamometer. Flaschentransportgeschwindigkeit: ca. 1 m/sMeasurement of the frictional resistance of 20 0.5 1 euro beer bottles filled with water as tension using a dynamometer. Bottle transport speed: approx. 1 m / s
Besprühen des Flaschentransportbandes mit 0,4 %iger Bandschmier¬ mitte11ösung, wie in den Beispielen genannt. Sprühleistung der Düsen: 4 1/h, 1 Düse pro Band.Spraying the bottle conveyor belt with 0.4% band lubricant solution, as mentioned in the examples. Spraying performance of the nozzles: 4 1 / h, 1 nozzle per belt.
Der im folgenden angegebene Reibbeiwert "μ" ergibt sich als der Quotient der gemessenen Zugspannung für eine Flasche zum Gewicht der Flasche in Gramm. Weiterhin wurden die Produkte mit Hartwasser (16 °d) nach den Be¬ stimmungen der DIN 53902 getestet.The coefficient of friction "μ" given below is the quotient of the measured tensile stress for a bottle to the weight of the bottle in grams. Furthermore, the products were tested with hard water (16 ° d) according to the provisions of DIN 53902.
Das Schaumverhalten wird nach folgenden Klassen beurteilt:The foam behavior is assessed according to the following classes:
0 = schaumfrei0 = foam-free
1 = vereinzelte Schaumblasen1 = isolated foam bubbles
2 = geringes Schäumen, nicht störend2 = low foaming, not disturbing
3 = Schäumen, störend3 = foaming, disturbing
4 = starkes Schäumen, nicht akzeptabel, Schaum unter dem Band4 = strong foaming, not acceptable, foam under the tape
Der Reibbeiwert sollte zur ausreichenden Schmierung bei oder kleiner gleich 0,10 bis 0,12 liegen. Bei Überschreiten von 0,15 läßt die Schmierwirkung und somit der einwandfreie Transport deut¬ lich nach.For sufficient lubrication, the coefficient of friction should be 0.10 to 0.12 or less. If the value exceeds 0.15, the lubricating effect and thus the problem-free transport clearly deteriorates.
Die Klarwasserlöslichkeit der Anwendungslösungen sollte auch über einen längeren Versuchszeitraum gewährleistet sein, um Ablagerungen in Kugelventilfiltern, Düsen, Sprüh- und VerteilSystem, Band und Transportgut zu vermeiden.The clear water solubility of the application solutions should also be guaranteed over a longer test period in order to avoid deposits in ball valve filters, nozzles, spray and distribution systems, belts and transport goods.
Die Schaumentwicklung sollte gering sein, da übermäßiger Schaum nicht nur den Arbeitsablauf (automatischer bottle inspector) und die Arbeitssicherheit (Rutschgefahr) stört, sondern darüber hinaus auch das Etikett aufweichen und in das noch nicht verschlossene Gefäß dringen kann. Zusätzlich wird durch übermäßige Schaumneigung der Reibbeiwert verschlechtert.The foam development should be low, since excessive foam not only interferes with the workflow (automatic bottle inspector) and occupational safety (risk of slipping), but also can soften the label and penetrate into the not yet sealed container. In addition, the coefficient of friction deteriorates due to excessive foaming tendency.
Tabelle 1Table 1
Cocosfetta in + 12E0 mittelstarke RisseCocosfetta in + 12E0 medium strong cracks
Oleylamid + 5E0 viele RisseOleylamide + 5E0 many cracks
2 Hydroxyfettalkoholethoxylat viele Risse2 hydroxy fatty alcohol ethoxylate many cracks
Oleyl-cetylpropylenglycolether viele RisseOleyl cetyl propylene glycol ether many cracks
Oleyl-cetylalkohol + 5E0 viele Risse Alkylbenzolsulfonat keine RisseOleyl cetyl alcohol + 5E0 many cracks Alkylbenzenesulfonate no cracks
Cocosalkyldimethylaminooxid keine RisseCocosalkyldimethylaminooxid no cracks
Cδ-10 Glycosidn=ι 5 (70 % Aktivsubstanz) fast keine RisseCδ-10 glycoside n = ι 5 (70% active substance) almost no cracks
Cß-io Glycosidn=if4 (60 % Aktivsubstanz) keine RisseCß-io glycoside n = i f 4 (60% active substance) no cracks
Cδ-10 G1ycosidn=l,7-l,8 fast keine RisseCδ-10 G1 y cos i d n = 1, 7-1, 8 almost no cracks
Anionische Tenside wie das Alkylbenzolsulfonat lassen sich nicht in die kationisch reagierenden Kettengleitmittel auf Alkylaminbasis einarbeiten, so daß nur noch Aminoxide und Alkylpolyglucoside für den Einsatz in entsprechenden Kettengleitmitteln verbleiben.Anionic surfactants such as alkylbenzenesulfonate cannot be incorporated into the cationically reacting chain lubricants based on alkylamines, so that only amine oxides and alkyl polyglucosides remain for use in corresponding chain lubricants.
Beispiel 1example 1
6 % Cocospropylendiammoniumacetat 6 % Cocosdipropylentriammoniumacetat 3 % Cocosalkyldimethylaminoxid 85 % Wasser6% coco propylene diammonium acetate 6% coco dipropylene triammonium acetate 3% coco alkyl dimethyl amine oxide 85% water
Reibbeiwert: 0,14 Schaumverhalten: schäumendFriction coefficient: 0.14 Foam behavior: foaming
Eignung: wenig Risse Klarwasserlöslichkeit: absolut klarSuitability: few cracks Clear water solubility: absolutely clear
Beispiel 2Example 2
6 % Cocospropylendiammoniumacetat 6 % Cocosdipropylentriammoniumacetat 3 % Cg-io Glycosidn=if4 (60 % Aktivsubstanz) 85 % Wasser6% coco propylene diammonium acetate 6% coco dipropylene triammonium acetate 3% Cg-io glycoside n = i f 4 (60% active substance) 85% water
Reibbeiwert: 0,10 Schaumverhalten: mäßig schäumendFriction coefficient: 0.10 Foam behavior: moderately foaming
Eignung: keine Rißb ldung Klarwasserlösl chkeit: absolut klar Verqleichsbeispiel 1Suitability: no cracking Clear water solubility: absolutely clear Comparative Example 1
8 % Laurylpropylendiammoniumacetat 4 % N.N-Dimethyl-N-laurylammoniumacetat 88 % Wasser8% laurylpropylene diammonium acetate 4% N.N-dimethyl-N-laurylammonium acetate 88% water
Reibbeiwert: 0,10 Schaumverhalten: nicht schäumendFriction coefficient: 0.10 Foam behavior: not foaming
PET-Eignung: wenig Risse Klarwasserlöslichkeit: opakPET suitability: few cracks. Clear water solubility: opaque
Veroleichsbeispiel 2Comparative example 2
6 % Cocospropylendiammoniumacetat 6 % Cocosdipropylentriammoniumacetat 88 % Wasser6% coconut propylene diammonium acetate 6% coconut dipropylene triammonium acetate 88% water
Reibbeiwert: 0,10 Schaumverhalten: schwach schäumendFriction coefficient: 0.10 Foam behavior: slightly foaming
PET-Eignung: keine Risse Klarwasserlöslichkeit: schwach opakPET suitability: no cracks. Clear water solubility: slightly opaque
Veroleichsbeispiel 3Comparative example 3
6 % Cocospropylendiammoniumacetat 6 % Cocosdipropylentriarnmoniumacetat 3 % Cocosfettamin + 12E0 85 % Wasser6% coconut propylene diammonium acetate 6% coconut dipropylene triarnmonium acetate 3% coconut fatty amine + 12E0 85% water
Reibbeiwert: 0,11 Schaumverhalten: schwach schäumendFriction coefficient: 0.11 Foam behavior: slightly foaming
PET-Eignung: starke Risse Klarwasserlöslichkeit: absolut klar PET suitability: strong cracks Clear water solubility: absolutely clear

Claims

P a t e n t a n s p r ü c h e Patent claims
1. Seifenfreie Schmiermittel auf der Basis von amphoteren Verbin¬ dungen, primäre, sekundären und/oder tertiären Aminen und/oder Salzen derartiger Amine der allgemeinen Formel (I), (Ila), (Ilb), (lila), (Illb), (Illb), (IIIc), (IVa) und (IVb)1. Soap-free lubricants based on amphoteric compounds, primary, secondary and / or tertiary amines and / or salts of such amines of the general formula (I), (Ila), (Ilb), (purple), (Illb), (Illb), (IIIc), (IVa) and (IVb)
R-[NH-(CH2)n]m - N - R3 - COOM (I)R- [NH- (CH 2 ) n ] m - N - R 3 - COOM (I)
R2R2
R -NH-R5 (Ha)R -NH-R5 (Ha)
R -NH-(CH2)3NH2 (Illa)R -NH- (CH 2 ) 3 NH 2 (Illa)
R4-NH-(CH2)3N+H3 x- (IIIb) R 4 -NH- (CH 2 ) 3 N + H 3 x- (IIIb)
R4-N+H2-(CH2)3-N+H32X- (IIIC)R 4 -N + H 2 - (CH 2 ) 3 -N + H 3 2X- (IIIC)
R -NR7R8 (IVa) und/oderR-NR7R8 (IVa) and / or
R -N+HR7R8 x- (IVb) wobeiR -N + HR7R8 x- (IVb) in which
R für einen gesättigten oder einfach oder mehrfach ungesättigten, linearen oder verzweigten Alkylrest mit 6 bis 22 C-Atomen, der gegebenenfalls durch -OH, -NH , -NH-, -C0-, -(CH CH 0)ι~ oder -(CH CH2CH20)-|- substituiert sein kann,R is a saturated or mono- or polyunsaturated, linear or branched alkyl radical having 6 to 22 carbon atoms, which may be replaced by -OH, -NH, -NH-, -C0-, - (CH CH 0) ι ~ or - ( CH CH 2 CH 2 0) - | - may be substituted,
R1 für Wasserstoff, einen Alkylrest mit 1 bis 4 C-Atomen, einen Hydroxyalkylrest mit 1 bis 4 C-Atomen oder einen Rest -R C00MR 1 represents hydrogen, an alkyl radical having 1 to 4 carbon atoms, a hydroxyalkyl radical having 1 to 4 carbon atoms or a radical -R C00M
R2 nur für den Fall, daß M eine negative Ladung darstellt für Was¬ serstoff, einen Alkylrest mit 1 bis 4 C-Atomen, oder einen Hy¬ droxyalkylrest mit 1 bis 4 C-Atomen,R2 only in the case where M represents a negative charge for hydrogen, an alkyl radical with 1 to 4 C atoms, or a hydroxyalkyl radical with 1 to 4 C atoms,
R3 für einen gesättigten oder einfach oder mehrfach ungesättigten, linearen oder verzweigten Alkylrest mit 1 bis 12 C-Atomen, der gegebenenfalls durch -OH, -NH2r -NH-, -C0-, -(CH2CH20)-|- oder -(CH2CH2CH20)-|- substituiert sein kann,R 3 is a saturated or mono- or polyunsaturated, linear or branched alkyl radical having 1 to 12 carbon atoms, which may be replaced by -OH, -NH 2r -NH-, -C0-, - (CH 2 CH 2 0) - | - or - (CH 2 CH 2 CH 2 0) - | - may be substituted,
R4 für einen substituierten oder unsubstituierten, linearen oder verzweigten, gesättigten oder einfach oder mehrfach ungesättig¬ ten Alkylrest mit 6 bis 22 C-Atomen, der als Substituenten min¬ destens einen Amin-, Imin-, Hydroxy-, Halogen- und/oder Car- boxyrest aufweisen kann, einen substituierten oder unsubstituierten Phenylrest, der als Substituenten mindestens einen Amin-, Imin-, Hydroxy-, Halo¬ gen-, Carboxy- und/oder einen linearen oder verzweigten, ge¬ sättigten oder einfach oder mehrfach ungesättigten Alkylrest mit 6 bis 22 C-Atomen aufweisen kann,R 4 is a substituted or unsubstituted, linear or branched, saturated or mono- or polyunsaturated alkyl radical having 6 to 22 carbon atoms, the substituents being at least one amine, imine, hydroxyl, halogen and / or Carboxy residue, a substituted or unsubstituted phenyl residue, which has at least one amine, imine, hydroxyl, halogen, carboxy and / or a linear or branched, saturated or mono- or polyunsaturated alkyl residue as a substituent can have 6 to 22 carbon atoms,
R5 fQr Wasserstoff oder - unabhängig von R4 - für einen Rest R4,R5 fQ r is hydrogen or - independently of R 4 - is a radical R 4,
X" für ein Anion aus der Gruppe Amidosulfonat, Nitrat, Halogenid, Sulfat, Hydrogencarbonat, Carbonat, Phosphat oder R6-C00~ steht, wobeiX "stands for an anion from the group amidosulfonate, nitrate, halide, sulfate, hydrogen carbonate, carbonate, phosphate or R6-C00 ~, where
R6 für Wasserstoff, einen substituierten oder unsubstituierten, linearen oder verzweigten Alkylrest mit 1 bis 20 C-Atomen oder Alkenylrest mit 2 bis 20 C-Atomen, die als Substituenten minde¬ stens einen Hydroxy-, Amin- oder Iminrest aufweisen können, oder einen substituierten oder unsubstituierten Phenylrest, der als Substituenten einen Alkylrest mit 1 bis 20 C-Atomen auf¬ weisen kann, steht, undR6 represents hydrogen, a substituted or unsubstituted, linear or branched alkyl radical having 1 to 20 carbon atoms or alkenyl radical having 2 to 20 carbon atoms, which may have at least one hydroxyl, amine or imine radical as a substituent, or a substituted radical or unsubstituted phenyl radical, the may have an alkyl radical having 1 to 20 carbon atoms as a substituent, and
R7 und R8 jeweils unabhängig voneinander für einen substituierten oder unsubstituierten, linearen oder verzweigten Alkylrest mit 1 bis 20 C-Atomen oder Alkenyl¬ rest mit 2 bis 20 C-Atomen, die als Substituenten mindestens einen Hydroxy-, Amin- oder I inrest aufweisen können, oder einen substituierten oder unsubstituierten Phenylrest, der als Substituenten einen Alkylrest mit 1 bis 20 C-Atomen aufweisen kann,R7 and R8 each independently of one another for a substituted or unsubstituted, linear or branched alkyl radical having 1 to 20 C atoms or alkenyl radical having 2 to 20 C atoms, which may have at least one hydroxyl, amine or I radical as substituents , or a substituted or unsubstituted phenyl radical which may have an alkyl radical with 1 to 20 C atoms as a substituent,
M für Wasserstoff, Alkalimetall, Ammonium, einen Alkylrest mit 1 bis 4 C-Atomen, einen Benzylrest oder eine negative Ladung, n für eine ganze Zahl im Bereich von 1 bis 12, für eine ganze Zahl im Bereich von 0 bis 5 undM for hydrogen, alkali metal, ammonium, an alkyl radical with 1 to 4 carbon atoms, a benzyl radical or a negative charge, n for an integer in the range from 1 to 12, for an integer in the range from 0 to 5 and
1 für eine Zahl im Bereich von 0 bis 5 steht,1 represents a number in the range from 0 to 5,
enthaltend Alkyldimethylaminoxide und/oder Alkyloligoglycoside als nichtionische Tenside.containing alkyldimethylamine oxides and / or alkyl oligoglycosides as nonionic surfactants.
2. Schmiermittel nach Anspruch 1, dadurch gekennzeichnet, daß in der allgemeinen Formel (I)2. Lubricant according to claim 1, characterized in that in the general formula (I)
R für einen gesättigten oder einfach oder mehrfach ungesättigten, linearen Alkylrest mit 10 bis 18 C-Atomen, der gegebenenfalls durch -C0- substituiert sein kann, insbesondere einen unsub¬ stituierten, gesättigten linearen Alkylrest mit 12 bis 14 C- Atomen,R represents a saturated or mono- or polyunsaturated, linear alkyl radical having 10 to 18 carbon atoms, which can optionally be substituted by -C0-, in particular an unsubstituted, saturated linear alkyl radical having 12 to 14 carbon atoms,
R1 für Wasserstoff, Alkylrest mit 1 bis 3 C-Atomen oder ein Rest -CH2CH 0H, insbesondere Wasserstoff oder Alkylrest mit 1 bis 3 C-Atomen,R 1 represents hydrogen, alkyl radical having 1 to 3 C atoms or a radical -CH 2 CH 0H, in particular hydrogen or alkyl radical having 1 to 3 C atoms,
R2 für Wasserstoff oder Alkylrest mit 1 bis 3 C-Atomen,R 2 represents hydrogen or an alkyl radical having 1 to 3 carbon atoms,
R3 für Methylen- oder Di-methylen-rest, insbesondere Methylenrest, M für Wasserstoff oder eine negative Ladung, n für 2 oder 3, insbesondere 2 m für 0, 1 oder 2, insbesondere 0, steht.R 3 represents a methylene or dimethylene radical, in particular a methylene radical, M is hydrogen or a negative charge, n is 2 or 3, in particular 2 m is 0, 1 or 2, in particular 0.
3. Schmiermittel nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß sie die Verbindungen der allgemeinen Formeln (I) bis (IV), in einer Menge von 1 bis 99 Gew.-%, bezogen auf die Gesamtformulie¬ rung, enthalten.3. Lubricant according to claim 1 or 2, characterized in that they contain the compounds of the general formulas (I) to (IV) in an amount of 1 to 99% by weight, based on the overall formulation.
4. Schmiermittel nach Anspruch 3, dadurch gekennzeichnet, daß sie die Verbindungen der allgemeinen Formeln (I) bis (IV), in einer Menge von 5 bis 15 Gew.-%, insbesondere 10 bis 12 Gew.-%, bezogen auf die Gesamtformulierung, enthalten.4. Lubricant according to claim 3, characterized in that it contains the compounds of the general formulas (I) to (IV) in an amount of 5 to 15% by weight, in particular 10 to 12% by weight, based on the total formulation , contain.
5. Schmiermittel nach Anspruch 1 bis 4, dadurch gekennzeichnet, daß sie zusätzlich Wasser und gegebenenfalls Zusatz- und/oder Hilfsstoffe enthalten.5. Lubricant according to claim 1 to 4, characterized in that they additionally contain water and optionally additives and / or auxiliaries.
6. Schmiermittel nach einem oder mehreren der Ansprüchen 1 bis 5, dadurch gekennzeichnet, daß das GewichtsVerhältnis von Verbindungen der allgemeinen Formel (I) zu den Verbindungen der Formeln (II), (III) und/oder (IV) im Bereich von 10 : 1 bis 1 : 10, insbesondere im Verhältnis 5 : 1 bis 1 : 1 eingestellt ist.6. Lubricant according to one or more of claims 1 to 5, characterized in that the weight ratio of compounds of the general formula (I) to the compounds of the formulas (II), (III) and / or (IV) in the range from 10: 1 to 1:10, in particular in a ratio of 5: 1 to 1: 1.
7. Schmiermittel nach einem oder mehreren der Ansprüche 1 bis 6, dadurch gekennzeichnet, daß sie als Hilfsstoffe Lösungsvermittler und/oder pH-Regulatoren enthalten.7. Lubricant according to one or more of claims 1 to 6, characterized in that they contain solubilizers and / or pH regulators as auxiliaries.
8. Schmiermittel nach einem oder mehreren der Ansprüchen 1 bis 7, dadurch gekennzeichnet, daß sie einen pH-Wert im Bereich von 4 bis 11, insbesondere im Bereich von 6 bis 9, aufweisen. 8. Lubricant according to one or more of claims 1 to 7, characterized in that they have a pH in the range from 4 to 11, in particular in the range from 6 to 9.
9. Schmiermittel nach einem oder mehreren der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß sie eine dynamische Viskosität von we¬ niger als 300 mPa.s, insbesondere im Bereich von 5 bis 100 mPa.s aufweisen.9. Lubricant according to one or more of claims 1 to 8, characterized in that they have a dynamic viscosity of less than 300 mPa.s, in particular in the range from 5 to 100 mPa.s.
10. Schmiermittel nach einem oder mehreren der Ansprüche 1 bis 9, dadurch gekennzeichnet, daß die Alkyldimethylaminoxide einen gerad- kettigen oder verzweigten, gesättigten, einfach oder mehrfach un¬ gesättigten Alkylrest mit 10 bis 18, insbesondere 12 bis 14 C-Ato¬ men aufweisen.10. Lubricant according to one or more of claims 1 to 9, characterized in that the alkyldimethylamine oxides have a straight-chain or branched, saturated, mono- or polyunsaturated alkyl radical having 10 to 18, in particular 12 to 14, C-atoms .
11. Schmiermittel nach einem oder mehreren der Ansprüche 1 bis 10, dadurch gekennzeichnet, daß die Alkyloligoglycoside Verbindungen der Formel (V)11. Lubricant according to one or more of claims 1 to 10, characterized in that the alkyl oligoglycoside compounds of the formula (V)
-^--HGjp (V) umfassen, wobei- ^ - HGjp (V), where
Rl für einen Alkylrest mit 4 bis 22 Kohlenstoffatomen, vorzugs¬ weise 8 bis 16 Kohlenstoffatomen, [G] für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und p für eine Zahl im Bereich von 1 bis 10 steht.R1 is an alkyl radical having 4 to 22 carbon atoms, preferably 8 to 16 carbon atoms, [G] is a sugar radical having 5 or 6 carbon atoms and p is a number in the range from 1 to 10.
12. Schmiermittel nach Anspruch 11, dadurch gekennzeichnet, daß die Alkyloligoglycoside sich von Aldosen und/oder Ketosen, insbesondere der Glucose ableiten.12. Lubricant according to claim 11, characterized in that the alkyl oligoglycosides are derived from aldoses and / or ketoses, in particular glucose.
13. Schmiermittel nach einem oder mehreren der Ansprüche 1 bis 12, dadurch gekennzeichnet, daß sie Alkyloligoglucoside enthalten.13. Lubricant according to one or more of claims 1 to 12, characterized in that they contain alkyl oligoglucosides.
14. Schmiermittel nach einem oder mehreren der Ansprüche 1 bis 13, dadurch gekennzeichnet, daß sie 1 bis 10 Gew.% an Alkyloligogly- cosiden und/oder A inoxiden enthalten. 14. Lubricant according to one or more of claims 1 to 13, characterized in that they contain 1 to 10% by weight of alkyl oligoglycosides and / or amines.
15. Verwendung der Schmiermittel nach einem der Ansprüche 1 bis 14 als Kettenschmiermittel in der Lebensmittelindustrie, insbesondere für automatische Ketten- und Bandschmieranlagen.15. Use of the lubricant according to one of claims 1 to 14 as chain lubricant in the food industry, in particular for automatic chain and belt lubrication systems.
16. Verwendung der Schmiermittel nach einem der Ansprüche 1 bis 14 zum Reinigen von Leergut, Maschinen und Anlagen in der Lebensmit¬ tel- und Getränkeindustrie. 16. Use of the lubricant according to one of claims 1 to 14 for cleaning empties, machines and systems in the food and beverage industry.
EP93904004A 1992-03-02 1993-02-22 Surface-active base for non-soap lubricants Expired - Lifetime EP0629235B1 (en)

Applications Claiming Priority (3)

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DE4206506 1992-03-02
DE4206506A DE4206506A1 (en) 1992-03-02 1992-03-02 TENSID BASIS FOR SOAP-FREE LUBRICANTS
PCT/EP1993/000413 WO1993018121A1 (en) 1992-03-02 1993-02-22 Surface-active base for non-soap lubricants

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