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EP3728155A1 - Composition de revêtement pour des contenants en verre - Google Patents

Composition de revêtement pour des contenants en verre

Info

Publication number
EP3728155A1
EP3728155A1 EP18826080.6A EP18826080A EP3728155A1 EP 3728155 A1 EP3728155 A1 EP 3728155A1 EP 18826080 A EP18826080 A EP 18826080A EP 3728155 A1 EP3728155 A1 EP 3728155A1
Authority
EP
European Patent Office
Prior art keywords
koh
coating composition
wax compound
coating
compound
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.)
Pending
Application number
EP18826080.6A
Other languages
German (de)
English (en)
Inventor
Leendert Cornelis Hoekman
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.)
Arkema BV
Original Assignee
Arkema BV
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
Priority claimed from EP17210519.9A external-priority patent/EP3502077A1/fr
Priority claimed from EP17210515.7A external-priority patent/EP3502076A1/fr
Application filed by Arkema BV filed Critical Arkema BV
Publication of EP3728155A1 publication Critical patent/EP3728155A1/fr
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D191/00—Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
    • C09D191/06—Waxes

Definitions

  • the present invention relates to a coating composition for glass container .
  • the present invention relates to the use of an aqueous composition comprising a coating composition suitable for returnable glass container and its process of application.
  • Hollow glass containers are produced from molten glass at molds at high temperatures. As the surface of these containers is fragile and in order to preserve the strength of the glass and to prevent any direct glass to glass contact of the respective containers in order to avoid damage, they are surface coated directly after forming of the container .
  • Such a coating includes tin or, titanium or other heat decomposable metallic or organometallic based compounds. This is the basis of the coating needed for protection of the glass container surface from damage such as abrasions and scratches, which result in a loss of strength for the glass container.
  • the need for high tensile strength in a glass container is particularly acute when containers are mass produced, move rapidly in close proximity along high speed conveyor lines.
  • the glass containers nowadays in glass container manufacturing a two-step coating is applied in order to obtain scratch resistance and slipperiness of the glass containers. So the glass containers typically receive two surface coatings, one at the hot end, just before annealing and one at the cold end just after annealing.
  • the so called hot-end coating is applied by means of chemical vapor deposition (CVD) of a metal containing compound on the freshly formed, hot and single or double line positioned glass containers, as mentioned before.
  • CVD chemical vapor deposition
  • CEC cold end coating
  • spraying means in form of an aqueous dispersion.
  • aqueous dispersion usually partly oxidized polyethylene wax dispersions are applied.
  • Glass containers can be recycled and reused. If reused, such returnable glass containers are collected, cleaned and refilled.
  • the cleaning step of returnable glass containers includes usually caustic washing. During the caustic washing the cold end coating but also the hot end coating are gradually eroded. Unprotected bare glass surface is exposed after a few cycles and scuffing begins. Therefore a protective coating can be re-applied after washing and before refilling. However the adhesion of the protective coating on the surface of the glass container could be much less than the initial cold end coating.
  • An objective of the present invention is to increase the life time of returnable glass containers.
  • An objective is to provide a coating composition that provides a protective coating on glass containers and especially returnable glass containers .
  • An objective is to provide a coating composition that provides a lubricating coating on glass containers and especially returnable glass containers.
  • Another objective of the present invention is to provide a coating composition that is washed of completely during the washing step of the returnable containers.
  • Still another objective of the present invention is to provide a coating composition that once applied, resists to the treatment of the recycled containers until they leave the filling plant.
  • Still an additional objective is to provide a process for applying a coating composition that is washed off completely during the washing step of the returnable containers and that resists to the treatment of the recycled containers until they leave the filling plant .
  • the document US 4,803,099 describes a modified polyethylene, methods for its preparation and methods for finishing the external surfaces of glass containers.
  • the modified polyethylene is suitable for cold-end coating of glass.
  • the modified polyethylene comprises acid amide groups .
  • the document GB 1,049,717 describes also a lubricous coating for glass.
  • the coating composition comprises a reaction product of polyvinyl alcohol, an emulsified polyethylene and an acid compound.
  • the document GB discloses a lubricity coating for plastics coated glass articles.
  • the coating comprises an ionic copolymer of an alpha- olefin and an alpha, beta-ethylenically unsatured carboxylic acid.
  • the document W02004/049219 discloses a protective coating applying method for returnable glass containers.
  • the protective coating is a paraffin based coating.
  • a coating composition comprising wax compound (Wl) having a melting point below 85°C, in particular below 83°C, provides a protective coating on glass containers, that is completely washed of during cleaning of glass containers .
  • a coating composition comprising wax compound (Wl) having a melting point below 85°C, in particular below 83°C, provides a lubricating coating on glass containers and especially returnable glass containers.
  • a coating composition comprising wax compound (Wl) having a melting point below 85°C, in particular below 83°C, provides a coating on the glass containers that is washed of completely during the washing step of the returnable containers and that resists to the treatment of the recycled containers until they leave the filling plant.
  • the present invention relates to a coating composition suitable for glass containers said coating composition comprises a wax compound (Wl) characterized in that the wax compound (Wl) has a melting point below 85°C in particular below 83°C.
  • the present invention relates to a coating composition for glass containers said coating composition comprises a wax compound (Wl) characterized in that that the wax compound (Wl) has a melting point below 85°C in particular below 83°C.
  • the present invention relates to a process for applying a coating composition on the surface of glass containers said coating composition comprises a wax compound (Wl) characterized in that that the wax compound (Wl) has a melting point below 85°C, in particular below 83°C, said coating composition is applied in form of an aqueous dispersion.
  • Wl wax compound
  • the present invention relates to the use of a coating composition for lubricating the surface of glass containers said coating composition comprises a wax compound (Wl) characterized in that the wax compound (Wl) has a melting point below 85°C in particular below 83°C.
  • a range is from x to y in the present invention, it is meant that the upper and lower limit of this range are included, equivalent to at least x and up to y.
  • the coating composition of the present invention comprises wax compound (Wl) that is a low melting point wax in comparison to the partly oxidized polyethylene waxes usually used.
  • the wax compound (Wl) can be pure or mixture of wax compounds, as long as the mixture is possessing the melting point as given below and preferably the melting point and saponification number as given below.
  • the melting point of the wax compound (Wl) is expressed as drop melting point.
  • the melting point is evaluated as drop melting point according to ISO 6244:1982.
  • the melting point of the wax compound (Wl) is below 85°C. More preferably the melting point of the wax compound (Wl) is below 84°C, still more preferably below 83°C, even still more preferably below 82°C, advantageously below 81°C and more advantageously below 80 °C.
  • the melting point of the wax compound (Wl) is above 60°C. Still more preferably the melting point of the wax compound (Wl) is above 61 °C, even still more preferably above 62 °C, even still more preferably above 63 °C, advantageously above 64 °C and more advantageously above 65 °C. [038] More preferably the melting point of the wax compound (Wl) is between 60°C and 85°C.
  • the melting point of the wax is between 61°C and 84°C, even still more preferably between 62°C and 83°C, even still more preferably between 63°C and 82°C, advantageously between 64 °C and 81 °C and more advantageously between 65 ° C and 80°C.
  • the saponification number of wax compound (Wl) is above 20 mg KOH/g. More preferably the saponification number of the wax compound (Wl) is above 25 mg KOH/g, still more preferably above 30 mg KOH/g, even still more preferably above 33 mg KOH/g, advantageously above 35 mg KOH/g and more advantageously above 40 mg KOH/g.
  • the saponification number of wax compound (Wl) is below 250 mg KOH/g. More preferably the saponification number of the wax compound (Wl) is below 225 mg KOH/g, still more preferably below 220 mg KOH/g, even still more preferably below 210 mg KOH/g, advantageously below 200 mg KOH/g and more advantageously below 190 mg KOH/g.
  • the saponification number of wax compound (Wl) is between 20 mg KOH/g and 250 mg KOH/g, still more preferably between 25 mg KOH/g and 225 mg KOH/g, even still more preferably between 30 mg KOH/g and 220 mg KOH/g, advantageously between 33 mg KOH/g and 210 mg KOH/g, more advantageously between 35 mg KOH/g and 200 mg KOH/g and even more advantageously between 40 mg KOH/g and 200 mg KOH/g.
  • the acid number of the wax compound (Wl) can be above 1 mg KOH/g. More preferably the acid number of the wax compound (Wl) is above 2 mg KOH/g, still more preferably above 2.5 mg KOH/g, even still more preferably above 3 mg KOH/g, advantageously above 3.5 mg KOH/g and more advantageously above 4 mg KOH/g.
  • the acid number can be measured according to ASTM D1386 "Standard Test Method for Acid Number (Empirical) of Synthetic and Natural Waxes".
  • the acid number of the wax compound (Wl) can be below 25 mg KOH/g. More preferably the acid number of the wax compound (Wl) is below 24 mg KOH/g, still more preferably below 23 mg KOH/g, even still more preferably below 22 mg KOH/g, advantageously below 21 mg KOH/g and more advantageously below 20 mg KOH/g.
  • the acid number of the wax compound (Wl) is between 2 mg KOH/g and 24 mg KOH/g, still more preferably between 2.5 mg KOH/g and 23 mg KOH/g, even still more preferably between 3 mg KOH/g and 22 mg KOH/g, advantageously between 3.5 mg KOH/g and 21 mg KOH/g and more advantageously between 4 mg KOH/g and 20 mg KOH/g.
  • the wax compound (Wl) can be made of natural or synthetic waxes or a mixture of blend of both .
  • Useful natural waxes include vegetable waxes, animal waxes and mixtures thereof, as long as they have the required melting point defined before .
  • wax compound (Wl) has the required melting point and saponification number as defined before .
  • the wax compound (Wl) according to the invention comprises at least 50wt% of a compound comprising an ester function, preferably 51wt, more preferably 52wt%, even more preferably 53wt%, advantageously 54wt% and more advantageously 55wt%.
  • the compound comprising an ester function or simply ester is preferably an organic ester.
  • the organic ester is made from at least an alcohol and a fatty acid.
  • the compound comprising the ester function can be a monoester, a diester, a triester or mixtures thereof.
  • the alcohol of the organic ester can have one or several hydroxyl groups.
  • the alcohol of the organic ester is water soluble.
  • water soluble is meant that the alcohol is either completely miscible with water or that it has a solubility greater than 0.005 mol/lOOg water at 1013mbar and 25°C.
  • solubility greater than 0.01 mol/lOOg water at 1013mbar and 25°C, and more preferably the solubility greater than 0.025 mol/lOOg water at 1013mbar and 25°C.
  • Examples of alcohols in the present invention are methanol, ethanol, propanol, butanol; pentanol, hexanol; 1,2 ethandiol; 1,3 propanediol; 1,2 propanediol; 1,4 butanediol; 1,2 butanediol; 1,3 butanediol; 1,5 pentanediol; 1,2 pentanediol; 1,3 pentanediol; 1,6 hexane diol; diethylene glycol, triethylene glycol; glycerol or mixtures thereof, but not limited to this list.
  • the fatty acid is chosen from long and very long chain hydrocarbons fatty acids.
  • the hydrocarbon has at least 12 carbon atoms, preferably at least 14 carbon atoms.
  • the hydrocarbon has at most 52 carbon atoms, preferably at most 50 carbons.
  • the hydrocarbon chain of the fatty acid can be a linear or branched alkyls, alkenyls.
  • Examples of the acid are lauric acid, tridecylic acid, myristic acid, pentadecylic acid, palmitic acid, margaric acid, stearic acid, nonadecylic acid, arachidic acid, heneicosylic acid, behenic acid, tricosylic acid, lignoceric acid, pentacosylic acid, cerotic acid, heptacosylic acid, montanic acid, nonacosylic acid, melissic acid, henatriacontylic acid, lacceroic acid, psyllic acid, geddic acid, ceroplastic acid, hexatriacontylic acid, heptatriacontanoic acid, octatriacontanoic acid, myristoleic acid, palmitoleic acid, sapienic acid, oleic
  • the organic ester that is made from at least an alcohol and a fatty acid, of the wax compound (Wl), can also be a mixture of different alcohols and fatty acids as listed above.
  • the wax compound (Wl) is chosen from a mixture comprising at least two compounds chosen from organic ester, fatty acid and alcohol .
  • the wax compound (Wl) is chosen from a mixture comprising at least two compounds chosen from, monoesters, diesters, triesters, hydroxy monoesters, hydroxypolyesters , acid esters, acid polyesters, hydrocarbons, fatty acids, fatty ICEs.
  • the ratio of free fatty acids and fatty alcohols is less than 80wt% in the wax compound (Wl) .
  • the wax compound (Wl) is chosen from a mixture comprising at least two compounds chosen from organic esters, hydrocarbons, fatty acids.
  • the ratio of free fatty acids is less than 80wt% in the wax compound (Wl)
  • the wax compound (Wl) is chosen from a mixture comprising aliphatic esters, w-hydroxycarboxylic acids and fatty alcohols.
  • the ratio of free fatty alcohols is less than 80wt% in the wax compound (Wl)
  • the wax compound (Wl) is chosen from a mixture comprising an ester from a diol and fatty acids.
  • the diol has less than 6 carbons.
  • All the above mentioned embodiments for the wax compound (Wl) comprise at least 50wt% of a compound comprising an ester function as defined before.
  • the wax compound (Wl) it has to have a melting point below 90°C and preferably below 85°C, even more preferably below 83°C.
  • the wax compound (Wl) having a melting point below 85°C, preferably below 83°C can be a mixture, the melting point is not a single peak, but could also be a range. However the melting range is below the indicated temperature.
  • wax compound (Wl) More preferably all the above mentioned embodiments for the wax compound (Wl) have a saponification number of wax compound (Wl) that is above 20 mg KOH/g.
  • the wax compound (Wl) used in the present invention has a low needle penetration.
  • low is meant that the needle penetration is less than 6*10 _1 mm, advantageously less than 5*10 _1 mm.
  • the needle penetration can be estimated according to ASTM D1321.
  • the coating composition coirqprising the wax compound (Wl) is made by contact between coating composition and the container with a coating application method.
  • the method can be spraying or dipping or a coating applicator.
  • the process comprises the steps of:
  • the coating composition that is applied comprises the wax compound (Wl) as defined before.
  • the means for applying the coating by spraying comprise spraying means .
  • the means for applying the coating by dipping comprise a recipient containing the coating composition in which the containers are dipped.
  • the coating applicator can be a brush, capillary, sponge, fibre or the like.
  • the coating material is applied on the surface of the container via the contact area between the coating applicator and container surface.
  • coating composition is applied by spraying.
  • the composition is applied at a temperature below 60°C, more preferably at a temperature below 50°C and even more preferably at a temperature below 45°C.
  • the temperature of the glass container during step ii) is preferably below 60°C, more preferably is below 50°C and even more preferably is below 45°C.
  • compositions comprising a wax compound (Wl)can adhere on the glass bottle at temperatures below 60°C, in particular at temperatures below 50 °C.
  • the coating composition comprising the wax compound (Wl) is preferably applied as an aqueous dispersion.
  • the aqueous dispersion comprises surfactant or surfactants and the wax compound (Wl) .
  • a dispersion according to the invention is a colloidal system at ambient temperature with a continuous liquid phase and a discontinuous solid phase that is distributed throughout the continuous phase.
  • ambient temperature is meant the interval between 20 °C and 25 °C.
  • the surfactant can be non-ionic, anionic, cationic or zwitterionic or mixture thereof.
  • the surfactant comprises less than 20% by weight of anionic surfactant relative to the total weight of the surfactant, preferably less than 10% relative to the total weight of the surfactant and even more preferably does not contains any anionic surfactant.
  • the surfactant ( s ) is chosen in the group consisting of non-ionic, cationic, zwitterionic, and mixture thereof, preferably is a cationic surfactant.
  • the coating composition applied on the surface of the glass containers comprises surfactant or surfactants and the wax compound (Wl) .
  • the quantity of the surfactant or surfactants in the coating composition is comprised between 0.5wt% and 50wt% relative to the coating composition applied comprising surfactant or surfactants and the wax compound (Wl) . In this calculation only the solids coating composition are considered namely the surfactant or surfactants and the wax compound (Wl) .
  • the quantity of the surfactant or surfactants in the coating composition is comprised between 5wt% and 50wt%, more preferably between 10wt% and 45wt%, still more preferably between 10wt% and 40wt%, even more preferably between 15wt% and 40wt%, advantageously between 20wt% and 40wt% and more advantageously between 20wt% and 40wt%.
  • the quantity of the wax compound (Wl) in the aqueous dispersion that is applied on the glass container may be expressed as ratio of wax compound (Wl) to water of from 1:5 to 1:2000, preferably from 1:10 to 1:1000.
  • the aqueous dispersion that is applied on the surface of a glass container comprises between 0.05wt% and 5wt% of coating composition comprising the wax compound (Wl) according to the invention .
  • the aqueous dispersion that is applied on the surface of a glass container comprises between 0.1 and 4wt% of coating composition comprising the wax compound (Wl) according to the invention, more preferably between 0.2 and 4wt%, still more preferably between 0.5wt% and 4wt% and even more preferably between 0.5wt% and 3.5wt% .
  • the coating composition comprising the wax compound (Wl) that is applied on the surface of a glass container as an aqueous dispersion can be obtained by dilution of a more concentrated dispersion.
  • the more concentrated aqueous dispersion comprising the wax compound (Wl) has a solid content between 5wt% and 50wt%, based on wax compound (Wl) and surfactant or surfactants.
  • the more concentrated aqueous dispersion comprising the wax compound (Wl) has a solid content between 5wt% and 60wt%, based on wax compound (Wl) and surfactant or surfactants, more preferably between 10wt% and 55wt%, still more preferably between
  • the process of applying the coating composition comprising the wax compound (Wl) according to the present invention can optionally comprise the additional step of diluting a more concentrated aqueous dispersion comprising the wax compound (Wl), before the step of applying the coating composition on the surface of a glass container.
  • the process of applying the coating composition comprising the wax compound (Wl) according to the present invention can optionally comprise the additional step of preparing a more concentrated aqueous dispersion comprising the wax compound (Wl), before the steps of diluting a more concentrated aqueous dispersion comprising the wax compound (Wl)and of applying the coating composition on the surface of a glass container .
  • the process of the invention can comprise a step i'), preferably before step i), of cleaning by washing the glass container with a washing composition comprising a zinc or aluminium compound at temperature of less than 90°C.
  • the cleaning or washing step i' it takes place at a temperature below 90°C.
  • the temperature refers to the temperature of the washing composition.
  • the temperature refers to the maximum temperature during the whole washing step.
  • the washing step may have sub steps.
  • the washing step is considered the cleaning or washing of the glass container, with the washing composition.
  • there are intermediate rinsing steps during the washing step that are below the indicated temperature interval or below the preferred minimal temperature.
  • the temperature of the washing step is below 88 °C, more preferably below 86°C, still more preferably below 84°C, even more preferably below 82°C.
  • the temperature of the washing step is above 40°C, more preferably above 50 °C.
  • the temperature of the washing step is between 40 °C and 88°C, more preferably between 50°C and 86°C.
  • the washing composition of the cleaning step of the process of the present invention is a zinc or aluminium compound and preferably the zinc or aluminium compound is in form of compound comprising a zinc or aluminium ion.
  • the source of aluminum ion and the source of zinc ion can be provided as organic salts, inorganic salts, and mixtures thereof.
  • Exemplary sources of zinc ions include zinc salts such as zinc chloride, zinc bromide, zinc sulfate, zinc nitrate, zinc iodide, zinc thiocyanate, zinc fluorosilicate, zinc dichromate, zinc chlorate, sodium zincate, zinc gluconate, zinc acetate, zinc benzoate, zinc citrate, zinc lactate, zinc formate, zinc bromate, zinc bromide, zinc fluoride, zinc fluosilicate , and zinc salicylate.
  • zinc salts such as zinc chloride, zinc bromide, zinc sulfate, zinc nitrate, zinc iodide, zinc thiocyanate, zinc fluorosilicate, zinc dichromate, zinc chlorate, sodium zincate, zinc gluconate, zinc acetate, zinc benzoate, zinc citrate, zinc lactate, zinc formate, zinc bromate, zinc bromide, zinc fluoride, zinc fluosilicate , and zinc salicylate.
  • the zinc salt is chosen from zinc chloride, zinc bromide, zinc iodide, zinc sulfate, zinc nitrate and zinc acetate.
  • Exemplary sources of aluminum ion include aluminum salts such as sodium aluminate, aluminum bromide, aluminum chlorate, aluminum chloride, aluminum iodide, aluminum nitrate, aluminum sulfate, aluminum acetate, aluminum formate, aluminum tartrate, aluminum lactate, aluminum oleate, aluminum bromate, aluminum borate, aluminum potassium sulfate, aluminum zinc sulfate and aluminum phosphate.
  • aluminum salts such as sodium aluminate, aluminum bromide, aluminum chlorate, aluminum chloride, aluminum iodide, aluminum nitrate, aluminum sulfate, aluminum acetate, aluminum formate, aluminum tartrate, aluminum lactate, aluminum oleate, aluminum bromate, aluminum borate, aluminum potassium sulfate, aluminum zinc sulfate and aluminum phosphate.
  • the washing composition comprises a zinc compound.
  • the washing composition comprises an aluminum compound.
  • the washing composition comprises a zinc and an aluminum compound.
  • the quantity of the zinc or aluminium ion in the washing composition is at least 0.00025mol/l, preferably at least 0.0005 mol/1, more preferably at least 0.001 mol/1 still more preferably at least 0.002 mol/1, advantageously at least 0.005 mol/1 and more advantageously at least 0.01 mol/1.
  • the quantity of the zinc or aluminium ion in the washing composition is at most 0.1mol/l, preferably at most 0.05mol/l and more preferably at most 0.04 mol/1, still more preferably at most 0.03 mol/1, advantageously at most 0.025mol/l and more advantageously at most 0.02mol/l .
  • the quantity of the zinc or aluminium ion in the washing composition is between 0.00025mol/l and 0.1mol/l, more preferably between 0.001 mol/1 and 0.04 mol/1, still more preferably between 0.002 mol/1 and 0.03 mol/1 , advantageously between 0.005 mol/1 and 0.025mol/l and more advantageously between 0.01mol/l and 0.02 mol/1.
  • the pH of the washing composition is at least 8. More preferably the pH of the washing composition is at least 12, still more preferably at least 12.5, advantageously at least 13, more advantageously at least 13.1 and most advantageously at least 13.2.
  • the pH of the washing composition is obtained by adding at least one alkaline source. The pH of the washing composition is measured with a pH meter.
  • the washing composition comprises one or more alkaline sources.
  • the alkali source can be chosen among compounds generating OH- ions in aqueous solution.
  • the alkaline source is an alkali metal hydroxide. This can be for example sodium hydroxide or potassium hydroxide.
  • hydroxide ions OH- In the washing composition there are hydroxide ions OH-.
  • the quantity of the OH- ions in the washing composition is at least 0.05mol/l, preferably at least 0.075mol/l, more preferably at least 0.1mol/l, still more preferably at least 0.15 mol/1 and advantageously at least 0.2 mol/1.
  • the quantity of the OH- ions in the washing composition is at most 2.5 mol/1, preferably at most 2 mol/1, still more preferably at most 1.5 mol/1 and advantageously at most 1 mol/1.
  • the quantity of the OH- ions in the washing composition is between 0.05mol/l and 2.5mol/l, more preferably between 0.075 mol/1 and 2 mol/1, still more preferably between 0.1 mol/1 and 1.5 mol/1 and advantageously between 0.2 mol/1 and 1 mol/1.
  • the molar ratio between the zinc or aluminium ion in the washing composition and the OH- ions in the washing composition is at least 0.002, preferably at least 0.0025, more preferably at least 0.003 and advantageously at least 0.005, and most advantageously at least 0.01.
  • the molar ratio between the zinc or aluminium ion in the washing composition and the OH- ions in the washing composition is at most 0.5, preferably at most 0.4, more preferably at most 0.3, advantageously at most 0.2 and most advantageously at most 0.1.
  • the molar ratio between the zinc or aluminium ion in the washing composition and the OH- ions in the washing composition is most advantageously between 0.01 and 0.10.
  • the molar quantity of the zinc or aluminium ion in the washing composition in function of the OH- ions in the washing composition is according to formula (1) :
  • C 2 is the concentration zinc or aluminium ion in the washing composition in mol/1
  • Ci is the concentration of the OH- ions in mol/1
  • B is a factor
  • A is a summand.
  • the summand A is between -0.001 and 0.04.
  • the factor B is between 0.025 and 0.045.
  • More preferably formula (1) applies especially to an interval of the concentration of the OH- ions from 0.05mol/l to lmol/1 and advantageously to an interval of the concentration of the OH- ions from 0. lmol/1 to lmol/1.
  • the glass container of the present invention is a bottle or a jar.
  • the bottle can be a beer, a milk or a soft drink bottle, wine bottles.
  • the glass container is a returnable glass container.
  • the thickness of the hot end coating is measured by method of estimation the amount of light reflection from a coated glass surface in comparison to a measurement taken from a known calibrated thickness standard with a Hot End Coating Measuring System from AGR International Inc..
  • a Miele disinfector type G7835 CD was used as a washing machine.
  • the effective washing time is 13.5 minutes and the total cycle time is 65 minutes.
  • the wash temperature was between 60°-80°C.
  • the line simulator used was an equipment from AGR International Inc. .Line simulation was done under wet conditions at a speed of 30rpm.
  • the pasteurization was made with a Miele disinfector type G7835, with program 3-pasteur at a water temperature of 65°C and a total cycle time of 40 minutes.
  • One cycle consists of washing (caustic washing) , coating application, line simulation for 1 minute, pasteurization, line simulation of 1 minute, samples are evaluated concerning the visual surface appearance of containers.
  • 50cl green glass or flint glass water bottles were used.
  • the bottles had a tin oxide hot end coating of between 40 and 55 CTU.
  • Candelilla Wax having a melting point (range) from 68.5°C to 72.5°C and a saponification value between 43 and 65 mg KOH/g was used as wax compound (Wl) here called (Wla) .
  • a wax compound comprising essentially C18-C36 acid glycol ester melting point of 72.6°C and a saponification value 169 mg KOH/g was used as wax compound (Wl) here called (Wlb) .
  • first comparative examples an oxidized polyethylene wax having a melting point (range) from 105°C to 111°C and a saponification value of less than 30 mg KOH/g was used as comparative here called (Cl) .
  • Aqueous dispersions of each wax compound were prepared at a solid content of 28wt% based on respective wax compound and surfactant. A cationic surfactant is used. [0127] The aqueous dispersions were diluted with additional water for obtaining a dispersion with lwt% solid content based on respective wax compound and surfactant. This diluted aqueous dispersion is applied on the container surface.
  • the coating was applied with a spray gun Walter Pilot WA XV from Walther Spritz- und Lackiersysteme GmbH.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
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  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Surface Treatment Of Glass (AREA)

Abstract

La présente invention concerne une composition de revêtement pour un contenant en verre. En particulier, l'invention concerne une composition de revêtement pour des contenants en verre consignés. La présente invention concerne l'utilisation d'une composition aqueuse comprenant une composition de revêtement appropriée pour un récipient en verre consigné et son procédé d'application.
EP18826080.6A 2017-12-22 2018-12-21 Composition de revêtement pour des contenants en verre Pending EP3728155A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP17210519.9A EP3502077A1 (fr) 2017-12-22 2017-12-22 Composition de revêtement pour récipients en verre
EP17210515.7A EP3502076A1 (fr) 2017-12-22 2017-12-22 Procédé de traitement de récipients en verre
PCT/EP2018/086746 WO2019122405A1 (fr) 2017-12-22 2018-12-21 Composition de revêtement pour des contenants en verre

Publications (1)

Publication Number Publication Date
EP3728155A1 true EP3728155A1 (fr) 2020-10-28

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EP18826080.6A Pending EP3728155A1 (fr) 2017-12-22 2018-12-21 Composition de revêtement pour des contenants en verre

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Country Link
EP (1) EP3728155A1 (fr)
CN (1) CN111757859A (fr)
SG (1) SG11202005031YA (fr)
WO (1) WO2019122405A1 (fr)

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Publication number Priority date Publication date Assignee Title
FR3111906B1 (fr) * 2020-06-24 2022-05-20 Arkema France Stabilisation cationique

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Publication number Priority date Publication date Assignee Title
US3357853A (en) 1964-01-02 1967-12-12 Ball Brothers Co Inc Lubricous coating for glass containing polyvinyl alcohol, emulsified polyethylene andan inorganic acid
US3445275A (en) * 1965-05-25 1969-05-20 Anchor Hocking Glass Corp Glass container coated with a lubricating film comprising carnauba wax and polyvinyl alcohol
DE2351801C3 (de) * 1973-10-16 1981-02-19 Centralin Gesellschaft Kircher Chemie Gmbh & Co Kg, 4020 Mettmann Verfahren zur Herstellung eines Wachsfilm-Überzuges auf Glasgegenständen, insbesondere Glasflaschen
US4001133A (en) * 1974-11-04 1977-01-04 Basf Wyandotte Corporation Method of washing glassware and inhibited cleaning solution and additive composition useful therein
DE3629146A1 (de) 1986-08-27 1988-03-03 Goldschmidt Ag Th Modifiziertes polyethylen, verfahren zu seiner herstellung und verwendung des modifizierten polyethylens zur verguetung der aeusseren oberflaechen von glasbehaeltern
US6363749B1 (en) * 1997-04-04 2002-04-02 Degussa Ag Process for manufacturing surface-sealed hollow glass containers
JP4464626B2 (ja) * 2002-05-17 2010-05-19 日本山村硝子株式会社 ガラス表面処理用コーティング組成物及びガラス製品
WO2004049219A1 (fr) 2002-11-22 2004-06-10 Axalto Sa Surveillance de l'utilisation de services dans un reseau de telecommunications
US7267743B2 (en) * 2003-03-17 2007-09-11 Marcus Oil And Chemical Wax emulsion coating applications
US7557071B2 (en) * 2004-10-21 2009-07-07 Johnsondiversy, Inc. Wax-based lubricants for conveyors
EP2202209A1 (fr) * 2008-12-23 2010-06-30 Arkema Vlissingen B.V. Revêtement occultant les rayures pour récipients en verre
US10413496B2 (en) * 2012-10-15 2019-09-17 L'oreal Aqueous wax dispersions
CN105330173A (zh) * 2015-09-30 2016-02-17 徐林波 玻璃表面防霉防伤新方法

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WO2019122405A1 (fr) 2019-06-27
SG11202005031YA (en) 2020-07-29
CN111757859A (zh) 2020-10-09

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