EP1001005A1 - Aqueous lubricant compositions - Google Patents

Aqueous lubricant compositions Download PDF

Info

Publication number
EP1001005A1
EP1001005A1 EP99121643A EP99121643A EP1001005A1 EP 1001005 A1 EP1001005 A1 EP 1001005A1 EP 99121643 A EP99121643 A EP 99121643A EP 99121643 A EP99121643 A EP 99121643A EP 1001005 A1 EP1001005 A1 EP 1001005A1
Authority
EP
European Patent Office
Prior art keywords
composition
carboxylate
alkyl
imidazoline
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP99121643A
Other languages
German (de)
French (fr)
Inventor
James Taylour
Christopher Thomas Wright
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.)
LHS UK Ltd
Original Assignee
LHS UK Ltd
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 LHS UK Ltd filed Critical LHS UK Ltd
Publication of EP1001005A1 publication Critical patent/EP1001005A1/en
Withdrawn legal-status Critical Current

Links

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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/16Ethers
    • 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
    • C10M133/38Heterocyclic nitrogen compounds
    • C10M133/44Five-membered ring containing nitrogen and carbon only
    • C10M133/46Imidazoles
    • 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
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/28Polyoxyalkylenes of alkylene oxides containing 2 carbon atoms only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/36Polyoxyalkylenes etherified
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • 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
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/108Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • C10M2215/224Imidazoles
    • 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

  • This invention relates to aqueous lubricant compositions suitable for use in the beverage and food industries.
  • While the present invention has broad applicability to the conveyance of containers it is envisaged to be particularly applicable to the conveyance of glass, plastic, plastic impregnated or coated cardboard, or metal beverage containers on belt or chain conveyors of metal or plastic.
  • the container is of glass a stainless steel conveyor is often used whereas, when the container is of another material, for example of aluminium, or of polyethylene terephthalate (PET) or of polyethylene (PE) the conveyor may be of, for example, of nylon or of polypropylene or an acetal resin.
  • Lubricant compositions are also subject to requirements other than those relating purely to their frictional performance.
  • Some lubricant compositions react with the hardness salts in water to deposit alkaline earth fatty acid salts on the conveyor and on the pipework used to deliver lubricant to the conveyor. This may be alleviated by ensuring that only soft water, for example containing hardness salts equivalent to below 5 ppm CaCO 3 , is used to make up the lubricant or by including an effective amount of a complexing agent, such as ethylene diamine tetra-acetic acid (EDTA), in the composition.
  • EDTA ethylene diamine tetra-acetic acid
  • Some lubricant compositions may tend to cause stress-cracking in the bases of plastic containers, such as PET containers, under conditions of internal pressurisation and/or warming. Using the lubricant compositions of the invention this effect may be reduced.
  • Some lubricant compositions amongst the fatty acid-, fatty amine- and phosphate ester-based compositions have a deleterious effect on print and tend to cause the leaching of printing ink from a print display. Since it is common practice to preprint beverage cans this presents a considerable problem.
  • U.S. patent specification No. 5 747 431 describes an aqueous lubricant composition containing one or more of a specific range of cyclic imidazolines defined by general formula and an amount of an inorganic acid or a carboxylic acid having up to 6 carbon atoms, for example acetic acid, sufficient to render the cyclic imidazoline soluble in water.
  • the quantity of the acid is typically from 0.05 to 10.5% by weight of the concentrate and, if required, additional acid is be added to bring the pH into the required region which is, preferably, from 3 to 8, more preferably from 3 to 6. At such a pH the imidazoline is solubilized by conversion to the acetate.
  • the lubricant composition may also contain an alkylamine carboxylate although this is exemplified in a quantity of only 0.6% wt/wt active raw material relative to 2.0% on an active basis, of the imidazoline.
  • U.K. patent specification No. 2 285 630-A describes an aqueous lubricant composition containing an alkylamine dicarboxylate, a cyclic imidazoline and an alkyl sulphonate anionic surfactant, each defined by general formula.
  • the present invention in its broadest aspect, is based on an aqueous lubricant composition comprising a combination of an amphoteric carboxylate with an imidazoline, the composition having a pH greater than 8, and on the finding that an unexpected degree of reduction in sliding friction obtainable by the use of such a composition, as well as certain other beneficial properties, in the absence of a content of any effective quantity of an anionic sulphonate surfactant, or of any other anionic surfactant.
  • any sulphonate or other anionic surfactant if present, is preferably present in less than 0.2%, particularly preferably less than 0.15% by weight of the composition.
  • cyclic imidazolines are believed to hydrolyse under some pH conditions with ring opening.
  • the present invention encompasses both cyclic imidazolines and the chain compounds corresponding to the cyclic imidazoline hydrolysis products, whether the chain compounds are actually formed by the hydrolysis mechanism or not, or whether they are formed in situ in the lubricant composition or not and the term "hydrolysis product", used hereafter, is intended to encompass all of these alternative possibilities.
  • the present invention provides an aqueous lubricant composition
  • aqueous lubricant composition comprising a combination of (a) one or more alkylamine monocarboxylates defined by the general formula (I) wherein
  • R 3 is an alkyl fatty chain, preferably of coco-distribution.
  • the preferred compounds within Formula (II) for use in the practice of the present invention are: and hydrolysis products thereof.
  • the lubricant compositions of the invention may be in the form of a concentrate, for example containing from 0.1% to 10% by weight, or up to the solubility limit, which may be up to 20% by weight or more, in total and on an active material basis, of the amphoteric alkyl carboxylate and the imidazoline.
  • a concentrate is preferably, but not essentially, produced using naturally soft water, distilled water or softened water to maximise storage stability.
  • the concentrate is further diluted, for example from 0.0005% to 5%, preferably at least 0.005%, preferably up to 2%, in total and on the same basis, of the same compounds. For this further dilution it is found that soft, medium or even hard water may be used.
  • the relative molar proportion of the amphoteric alkyl carboxylate and the imidazoline is preferably from 10:90 to 90:10, particularly preferably from 60:40 to 40:60.
  • the lubricant compositions may contain other constituents, for example a hydrophilic organic co-solvent such as, for example butyl diglycol, monoethylene glycol or isopropyl alcohol, suitably in a concentration of from 1% to 10% by weight, a nonionic surfactant such as an alcohol alkoxylate, suitably in a concentration of 0.1% to 5% by weight and a biocide, suitably in a concentration of from 0.1% to 10% by weight.
  • a hydrophilic organic co-solvent such as, for example butyl diglycol, monoethylene glycol or isopropyl alcohol, suitably in a concentration of from 1% to 10% by weight
  • a nonionic surfactant such as an alcohol alkoxylate
  • a biocide suitably in a concentration of from 0.1% to 10% by weight.
  • the cosolvent may be supplied by using the amphoteric carboxylate in the form of a solution thereof.
  • the pH of the lubricant composition of the invention is controlled at a pH greater than 8.5 for example, desirably, greater than 9. It is preferred that the pH is below 11 and a pH range of from 9.5 to 10.5 is particularly preferred.
  • the imidazoline is, surprisingly, solubilized in the presence of the alkylamine carboxylate. There is no reliance on salt formation to achieve solution in water.
  • the effectiveness of the lubricant compositions may be tested as follows.
  • a number of glass bottles sufficient to give a load of 2000g are placed on a pilot conveyor fitted with a stainless steel track.
  • the bottles are tethered to a force gauge capable of measuring the drag force in grams.
  • Lubricant at a suitable concentration is sprayed onto the track and the track set in motion.
  • Drag Coefficient (U) is calculated as Drag Force/2000 g.
  • a coefficient of less than 0.15 represents good lubrication and higher values represent poor lubrication.
  • Pressurised PET bottles are dipped into a sample of lubricant prediluted to use concentration (typically 1% by weight). After 10 minutes the bottles are removed and placed in an oven at a temperature of 38°C. After 72 hours at this temperature the bottles are removed and are examined visually for signs of stress cracking. A bottle similarly oven treated, which had not been contacted with the lubricant is used as a control.
  • Samples of steel sheet printed with a representative ink are immersed in solutions of the lubricant having up to 10 times normal use concentration. The solutions are held at a temperature of 60°C for 30 minutes and the samples were then removed and examined visually for ink leaching.
  • Example 1 used both the essential components of the invention, the imidazoline was absent from Example 2 and the amphoteric alkyl amine carboxylate was absent from Example 3. A synergic effect is apparent in the composition according to the invention from the results.
  • Example 4 composition was further diluted to 1% in water containing 10ppm sulphate or 10ppm phosphate ions. Both solutions remained clear overnight. This is in contrast to cationic lubricants, such as those based on fatty amines, which tend to become cloudy on standing as a result of the formation of insoluble sulphate or phosphate salts.
  • Example 5 composition was tested in waters ranging from 30 to 250 ppm CaCO 3 of hardness with no observable difference in Drag Coefficient. All the solutions remained clear despite the absence of a chelating agent.
  • lubricant compositions of the invention were found to be compatible with Can Print Pigments and PET.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

An aqueous lubricant composition, suitable for conveyor lubrication in the beverage or food industries, for example for lubricating the transport of glass, plastic, plastic impregnated or coated cardboard or metal beverage containers on a conveyor of stainless steel or nylon, comprises a combination of an amphoteric carboxylate, preferably an alkyl amine carboxylate, and an imidazoline, the composition having a pH above 8 and being in the absence of any effective quantity of an anionic sulphonate surfactant. The composition gives an excellent drag coefficient, is compatible with printing inks and gives low stress cracking in PET containers.

Description

  • This invention relates to aqueous lubricant compositions suitable for use in the beverage and food industries.
  • In the beverage and food industries product containers, such as bottles or cans, are commonly transported on continuously operating conveyors through unit operation stations, such as filling, closure or sealing stations. During transport between the stations, or at each operation, blockages of the containers on the conveyor can occur while the conveyor continues to move. To cope with these interruptions and resumptions in the movement of the containers reliably a low but appreciable sliding friction between the material of the containers and of the conveyor is required. It is usual to use a lubricant on the conveyor to achieve the required frictional characteristics. Additional functions of a lubricant are to provide control of microbiological growth and to provide detergency to remove spillages and other soils.
  • While the present invention has broad applicability to the conveyance of containers it is envisaged to be particularly applicable to the conveyance of glass, plastic, plastic impregnated or coated cardboard, or metal beverage containers on belt or chain conveyors of metal or plastic. When the container is of glass a stainless steel conveyor is often used whereas, when the container is of another material, for example of aluminium, or of polyethylene terephthalate (PET) or of polyethylene (PE) the conveyor may be of, for example, of nylon or of polypropylene or an acetal resin.
  • Lubricant compositions are also subject to requirements other than those relating purely to their frictional performance. Some lubricant compositions, for example those based on fatty acids, react with the hardness salts in water to deposit alkaline earth fatty acid salts on the conveyor and on the pipework used to deliver lubricant to the conveyor. This may be alleviated by ensuring that only soft water, for example containing hardness salts equivalent to below 5 ppm CaCO3, is used to make up the lubricant or by including an effective amount of a complexing agent, such as ethylene diamine tetra-acetic acid (EDTA), in the composition. Some lubricant compositions, for example those based on fatty amines, may tend to cause stress-cracking in the bases of plastic containers, such as PET containers, under conditions of internal pressurisation and/or warming. Using the lubricant compositions of the invention this effect may be reduced. Some lubricant compositions amongst the fatty acid-, fatty amine- and phosphate ester-based compositions have a deleterious effect on print and tend to cause the leaching of printing ink from a print display. Since it is common practice to preprint beverage cans this presents a considerable problem.
  • U.S. patent specification No. 5 747 431 describes an aqueous lubricant composition containing one or more of a specific range of cyclic imidazolines defined by general formula and an amount of an inorganic acid or a carboxylic acid having up to 6 carbon atoms, for example acetic acid, sufficient to render the cyclic imidazoline soluble in water. The quantity of the acid is typically from 0.05 to 10.5% by weight of the concentrate and, if required, additional acid is be added to bring the pH into the required region which is, preferably, from 3 to 8, more preferably from 3 to 6. At such a pH the imidazoline is solubilized by conversion to the acetate. Optionally, the lubricant composition may also contain an alkylamine carboxylate although this is exemplified in a quantity of only 0.6% wt/wt active raw material relative to 2.0% on an active basis, of the imidazoline.
  • U.K. patent specification No. 2 285 630-A describes an aqueous lubricant composition containing an alkylamine dicarboxylate, a cyclic imidazoline and an alkyl sulphonate anionic surfactant, each defined by general formula.
  • The present invention, in its broadest aspect, is based on an aqueous lubricant composition comprising a combination of an amphoteric carboxylate with an imidazoline, the composition having a pH greater than 8, and on the finding that an unexpected degree of reduction in sliding friction obtainable by the use of such a composition, as well as certain other beneficial properties, in the absence of a content of any effective quantity of an anionic sulphonate surfactant, or of any other anionic surfactant. For example, any sulphonate or other anionic surfactant, if present, is preferably present in less than 0.2%, particularly preferably less than 0.15% by weight of the composition.
  • In defining the composition provided by the invention it is noted that cyclic imidazolines are believed to hydrolyse under some pH conditions with ring opening. The present invention encompasses both cyclic imidazolines and the chain compounds corresponding to the cyclic imidazoline hydrolysis products, whether the chain compounds are actually formed by the hydrolysis mechanism or not, or whether they are formed in situ in the lubricant composition or not and the term "hydrolysis product", used hereafter, is intended to encompass all of these alternative possibilities.
  • The present invention provides an aqueous lubricant composition comprising a combination of (a) one or more alkylamine monocarboxylates defined by the general formula (I)
    Figure 00040001
       wherein
  • R1 represents C1 to C24, preferably C7 to C24, alkyl- or C1 to C24, preferably C7 to C24, alkyl-[N-(CH2)n']m- wherein n,n' and m are the same or different and have values of at least 1, preferably from 1 to 5
  • R2 represents H, C1 to C24 alkyl or C1 to C24 alkyl substituted by one or more hydroxyl or amine groups
  • M+ represents H+, Na+, K+ or (CH2OH.CH2)3NH+
  •    and (b)
       one or more cyclic imidazolines defined by the general formula (II), and hydrolysis products thereof,
    Figure 00040002
    wherein
    • R4 is -CH2-CH2-OH or -CH2-CH2-NH2 or is an amide function
    • R5 is an alkyl chain having a value of at least C1, preferably from C1 to C30.
  • The preferred compounds within Formula (I) for use in the practice of the present invention are:
    Figure 00040003
       wherein R3 is an alkyl fatty chain, preferably of coco-distribution.
  • The preferred compounds within Formula (II) for use in the practice of the present invention are:
    Figure 00050001
       and hydrolysis products thereof.
  • The lubricant compositions of the invention may be in the form of a concentrate, for example containing from 0.1% to 10% by weight, or up to the solubility limit, which may be up to 20% by weight or more, in total and on an active material basis, of the amphoteric alkyl carboxylate and the imidazoline. Such a concentrate is preferably, but not essentially, produced using naturally soft water, distilled water or softened water to maximise storage stability. For use the concentrate is further diluted, for example from 0.0005% to 5%, preferably at least 0.005%, preferably up to 2%, in total and on the same basis, of the same compounds. For this further dilution it is found that soft, medium or even hard water may be used. The relative molar proportion of the amphoteric alkyl carboxylate and the imidazoline is preferably from 10:90 to 90:10, particularly preferably from 60:40 to 40:60.
  • The lubricant compositions may contain other constituents, for example a hydrophilic organic co-solvent such as, for example butyl diglycol, monoethylene glycol or isopropyl alcohol, suitably in a concentration of from 1% to 10% by weight, a nonionic surfactant such as an alcohol alkoxylate, suitably in a concentration of 0.1% to 5% by weight and a biocide, suitably in a concentration of from 0.1% to 10% by weight. The cosolvent may be supplied by using the amphoteric carboxylate in the form of a solution thereof.
  • Preferably, to enhance solubility, the pH of the lubricant composition of the invention is controlled at a pH greater than 8.5 for example, desirably, greater than 9. It is preferred that the pH is below 11 and a pH range of from 9.5 to 10.5 is particularly preferred. At the pH levels envisaged by this invention the imidazoline is, surprisingly, solubilized in the presence of the alkylamine carboxylate. There is no reliance on salt formation to achieve solution in water.
  • The effectiveness of the lubricant compositions may be tested as follows.
  • Lubrication.
  • A number of glass bottles sufficient to give a load of 2000g are placed on a pilot conveyor fitted with a stainless steel track. The bottles are tethered to a force gauge capable of measuring the drag force in grams. Lubricant at a suitable concentration is sprayed onto the track and the track set in motion. Drag Coefficient (U) is calculated as Drag Force/2000 g. A coefficient of less than 0.15 represents good lubrication and higher values represent poor lubrication.
  • PET Compatibility.
  • Pressurised PET bottles are dipped into a sample of lubricant prediluted to use concentration (typically 1% by weight). After 10 minutes the bottles are removed and placed in an oven at a temperature of 38°C. After 72 hours at this temperature the bottles are removed and are examined visually for signs of stress cracking. A bottle similarly oven treated, which had not been contacted with the lubricant is used as a control.
  • Ink compatibility.
  • Samples of steel sheet printed with a representative ink are immersed in solutions of the lubricant having up to 10 times normal use concentration. The solutions are held at a temperature of 60°C for 30 minutes and the samples were then removed and examined visually for ink leaching.
  • Certain lubricant compositions according to the invention are now described with reference to the following examples but without any limitation of the scope of the invention thereto. Examples 1, 4 and 5 are according to the invention and Examples 2 and 3 are not according to the invention but are comparative therewith.
  • Examples 1-3.
  • The following compositions were made up by adding the other ingredients to the water and the compositions were tested for Drag Coefficient at a dilution of 1% by weight in tap water.
    Example No. 1 2 3
    Distilled water 85 87 90
    Butyl diglycol 2 2 2
    Nonionic alcohol alkoxylate 2 2 2
    Amphoteric 2.5 2.5 2.5
    Biocide 1.5 1.5 1.5
    Imidazoline 2 0 2
    Amphoteric alkyl amine
    carboxylate 5 5 0
    pH 10 9 11
    Drag Coefficient 0.075 0.1 0.15
  • Example 1 used both the essential components of the invention, the imidazoline was absent from Example 2 and the amphoteric alkyl amine carboxylate was absent from Example 3. A synergic effect is apparent in the composition according to the invention from the results.
  • Examples 4-5.
  • The following compositions were made up and tested for Drag Coefficient at a dilution of 0.5% by weight in tap water.
    Example No. 4 5
    Distilled water 89 89
    Nonionic alcohol alkoxylate 0.5 0.5
    Biocide 4 4
    Imidazoline 80H (R5 = C8) 1.5 0
    Imidazoline120H (R5 = C12) 0 1.5
    Amphoteric alkyl amine
    carboxylate 5 5
    pH 10 10
    Drag Coefficient 0.11 0.11
    Trade names/sources of constituents
  • These Examples show no difference between the Imidazolines having chains of 8 and of 12 carbon atoms. This is surprising since the longer chain length (C12 to C18) has traditionally been preferred.
  • Variations in the Examples.
  • The Example 4 composition was further diluted to 1% in water containing 10ppm sulphate or 10ppm phosphate ions. Both solutions remained clear overnight. This is in contrast to cationic lubricants, such as those based on fatty amines, which tend to become cloudy on standing as a result of the formation of insoluble sulphate or phosphate salts.
  • The Example 5 composition, further diluted to 1% by weight, was tested in waters ranging from 30 to 250 ppm CaCO3 of hardness with no observable difference in Drag Coefficient. All the solutions remained clear despite the absence of a chelating agent.
  • Other tests.
  • Using the test methods given above lubricant compositions of the invention were found to be compatible with Can Print Pigments and PET.
  • Experiments were conducted using other surfactant acids including sarcosinates, phosphate esters, ether carboxylates and sulphonic acids. The are less effective in that either the formulations are not hard water stable, have poor lubrication or have poor stability. However, it is likely that stability could be improved by the use of suitable cosolvents or surfactants.
  • A solution containing 1.5% by weight of Imidazoline 80H and 98.5% by weight of butyl diglycol was made up. It was found to have a pH of 10.5 which is very close to the pH levels in the preceding Examples. This is taken to indicate that the imidazoline is present in a similar form in the Examples as in the present test.

Claims (14)

  1. An aqueous lubricant composition, suitable for conveyor lubrication in the beverage or food industries, comprising a combination of an amphoteric carboxylate and an imidazoline, the composition having a pH above 8 and being in the absence of any effective quantity of an anionic sulphonate surfactant.
  2. A composition as claimed in claim 1 wherein the carboxylate is an amphoteric alkyl amine carboxylate.
  3. A composition as claimed in claim 2 wherein the carboxylate is a monocarboxylate.
  4. An aqueous lubricant composition, suitable for conveyor lubrication in the beverage or food industries, comprising a combination of
    (a) one or more alkylamine monocarboxylates defined by the general formula (I)
    Figure 00100001
       wherein
    R1 represents C1 to C24, preferably C7 to C24, alkyl- or C1 to C24, preferably C7 to C24, alkyl-[N-(CH2)n']m- wherein n, n' and m are the same or different and have values of at least 1, preferably from 1 to 5.
    R2 represents H, C1 to C24 alkyl or C1 to C24 alkyl substituted by one or more hydroxyl or amine groups
    M+ represents H+, Na+, K+ or (CH2OH.CH2)3NH+ and
    (b) one or more cyclic imidazolines defined by the general formula (II), and hydrolysis products thereof ,
    Figure 00110001
    wherein
    R4 is - CH2-CH2-OH or -CH2-CH2-NH2 or is an amide function
    R5 is an alkyl chain having a value of at least C1, preferably from C1 to C30.
    the composition having a pH above 8.
  5. A composition as claimed in claim 4 wherein the one or more alkylamine monocarboxylates is as defined by formula (III)
    Figure 00110002
  6. A composition as claimed in claim 4 wherein the one or more imidazolines is as defined by formula (IV)
    Figure 00110003
    and hydrolysis products thereof.
  7. A composition as claimed in any preceding claim in the form of a concentrate containing from 0.1% by weight, to the solubility limit, in total and on an active material basis of the amphoteric carboxylate and the imidazoline.
  8. A composition as claimed in any preceding claim in the form of a working solution containing from 0.0005% to 5% by weight, in total and on an active material basis, of the amphoteric carboxylate and the imidazoline.
  9. A composition as claimed in any preceding claim containing the amphoteric carboxylate and the imidazoline in relative molar proportions of from 10:90 to 90:10.
  10. A composition as claimed in any preceding claim having a pH greater than 8.5.
  11. A composition as claimed in claim 10 having a pH from 9.5 to 10.5.
  12. A composition as claimed in any preceding claim containing one or more of a hydrophilic organic co-solvent in a concentration of from 1% to 10% by weight, a nonionic surfactant in a concentration of 0.1% to 5% by weight and a biocide, in a concentration of from 0.1% to 10% by weight.
  13. The use of a composition as claimed in any preceding claim in conveyor lubrication.
  14. The use claimed in claim 13 wherein the conveyor is of stainless steel, polypropylene or an acetal resin and the containers to be conveyed are of glass, aluminium, steel, polyethylene terephthalate(PET), polyethylene(PE) or cardboard.
EP99121643A 1998-11-09 1999-10-30 Aqueous lubricant compositions Withdrawn EP1001005A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9824396A GB2343460B (en) 1998-11-09 1998-11-09 Aqueous lubricant compositions
GB9824396 1998-11-09

Publications (1)

Publication Number Publication Date
EP1001005A1 true EP1001005A1 (en) 2000-05-17

Family

ID=10842004

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99121643A Withdrawn EP1001005A1 (en) 1998-11-09 1999-10-30 Aqueous lubricant compositions

Country Status (2)

Country Link
EP (1) EP1001005A1 (en)
GB (1) GB2343460B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011008131A2 (en) * 2009-07-16 2011-01-20 Naumov Vladimir Nikolaevich Water-soluble conveyor lubricant
US9359579B2 (en) 2010-09-24 2016-06-07 Ecolab Usa Inc. Conveyor lubricants including emulsions and methods employing them
US9365798B2 (en) 2005-03-15 2016-06-14 Ecolab Usa Inc. Lubricant for conveying containers
US9562209B2 (en) 2005-03-15 2017-02-07 Ecolab Usa Inc. Dry lubricant for conveying containers
US9873853B2 (en) 2013-03-11 2018-01-23 Ecolab Usa Inc. Lubrication of transfer plates using an oil or oil in water emulsions

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2285630A (en) * 1994-01-12 1995-07-19 Diversey Corp Aqueous lubricant compositions for conveyor tracks
US5747431A (en) * 1994-01-12 1998-05-05 Diversey Lever Inc. Lubricant compositions

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2285630A (en) * 1994-01-12 1995-07-19 Diversey Corp Aqueous lubricant compositions for conveyor tracks
US5747431A (en) * 1994-01-12 1998-05-05 Diversey Lever Inc. Lubricant compositions

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9926511B2 (en) 2005-03-15 2018-03-27 Ecolab Usa Inc. Lubricant for conveying containers
US10815448B2 (en) 2005-03-15 2020-10-27 Ecolab Usa Inc. Lubricant for conveying containers
US10851325B2 (en) 2005-03-15 2020-12-01 Ecolab Usa Inc. Dry lubricant for conveying containers
US9365798B2 (en) 2005-03-15 2016-06-14 Ecolab Usa Inc. Lubricant for conveying containers
US9562209B2 (en) 2005-03-15 2017-02-07 Ecolab Usa Inc. Dry lubricant for conveying containers
WO2011008131A3 (en) * 2009-07-16 2011-03-10 Naumov, Vladimir Nikolaevich Water-soluble conveyor lubricant
WO2011008131A2 (en) * 2009-07-16 2011-01-20 Naumov Vladimir Nikolaevich Water-soluble conveyor lubricant
US10793806B2 (en) 2010-09-24 2020-10-06 Ecolab Usa Inc. Conveyor lubricants including emulsions and methods employing them
US10260020B2 (en) 2010-09-24 2019-04-16 Ecolab Usa Inc. Conveyor lubricants including emulsions and methods employing them
US9359579B2 (en) 2010-09-24 2016-06-07 Ecolab Usa Inc. Conveyor lubricants including emulsions and methods employing them
US9873853B2 (en) 2013-03-11 2018-01-23 Ecolab Usa Inc. Lubrication of transfer plates using an oil or oil in water emulsions
US10316267B2 (en) 2013-03-11 2019-06-11 Ecolab Usa Inc. Lubrication of transfer plates using an oil or oil in water emulsions
US10844314B2 (en) 2013-03-11 2020-11-24 Ecolab Usa Inc. Lubrication of transfer plates using an oil or oil in water emulsions
US11312919B2 (en) 2013-03-11 2022-04-26 Ecolab Usa Inc. Lubrication of transfer plates using an oil or oil in water emulsions
US11788028B2 (en) 2013-03-11 2023-10-17 Ecolab Usa Inc. Lubrication of transfer plate using an oil or oil in water emulsions

Also Published As

Publication number Publication date
GB2343460A (en) 2000-05-10
GB9824396D0 (en) 1998-12-30
GB2343460B (en) 2002-12-24

Similar Documents

Publication Publication Date Title
CA2382689C (en) Antimicrobial lubricants useful for lubricating containers, such as beverage containers, and conveyors therefor
JP4177458B2 (en) Lubricants for conveyor belt equipment in the food industry.
EP0847437B1 (en) Alkyl ether amine conveyor lubricant
US6372698B1 (en) Lubricant for chain conveyor belts and its use
AU660000B2 (en) Antimicrobial lubricant including fatty acid and quaternary ammonium compound
US5391308A (en) Lubricant for transport of P.E.T. containers
US6667283B2 (en) Antimicrobial, high load bearing conveyor lubricant
EP0847436B1 (en) Alkyl ether amine conveyor lubricants containing corrosion inhibitors
EP0990018B1 (en) Alkaline ether amine conveyor lubricant
JP2002527574A (en) Method for lubricating conveyor systems with lubricants containing phosphate esters of ethoxylated fatty acid amides
EP0706555B1 (en) Composition for inhibiting stress cracks in plastic articles and methods of use therefor
US20040167044A1 (en) Conveyor lubricants for use in the food and beverage industries
US5900392A (en) Aqueous belt lubricant composition based on fatty alkyl propylene tettramines and fatty alcohol polyglycol ethers and method for lubricating belt conveyor systems
EP1001005A1 (en) Aqueous lubricant compositions
EP1047758B1 (en) Antimicrobial, beverage compatible conveyor lubricant
WO2004037960A1 (en) Use of ether carboxylates as lubricants
US6548455B1 (en) Chain lubricant for conveyor and transport systems
US20060046940A1 (en) Aqueous conveyor and cutting lubricant
JP6438316B2 (en) Lubricant composition for belt conveyor and method for improving lubricity of belt conveyor
JP3994536B2 (en) Lubricant composition
WO1999061567A1 (en) Lubricant compositions
MXPA01003733A (en) Method of lubricating a conveyor system with a lubricant containing a phosphate ester of an ethoxylated fatty acid amide
MXPA96002746A (en) Lubrican compositions

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE FR LI NL

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

17P Request for examination filed

Effective date: 20000922

AKX Designation fees paid

Free format text: AT BE CH DE FR LI NL

17Q First examination report despatched

Effective date: 20020524

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20020403