+

WO2018185094A1 - Compositions de revêtement contenant un polymère fonctionnel hydroxyphényle et un polymère de latex - Google Patents

Compositions de revêtement contenant un polymère fonctionnel hydroxyphényle et un polymère de latex Download PDF

Info

Publication number
WO2018185094A1
WO2018185094A1 PCT/EP2018/058480 EP2018058480W WO2018185094A1 WO 2018185094 A1 WO2018185094 A1 WO 2018185094A1 EP 2018058480 W EP2018058480 W EP 2018058480W WO 2018185094 A1 WO2018185094 A1 WO 2018185094A1
Authority
WO
WIPO (PCT)
Prior art keywords
coating
polymer
solution
coating compositions
coating composition
Prior art date
Application number
PCT/EP2018/058480
Other languages
English (en)
Inventor
Jennifer WOJTALEWICZ
Alexander Polykarpov
Original Assignee
Akzo Nobel Coatings International B.V.
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 Akzo Nobel Coatings International B.V. filed Critical Akzo Nobel Coatings International B.V.
Priority to CA3056987A priority Critical patent/CA3056987A1/fr
Priority to ES18713708T priority patent/ES2881620T3/es
Priority to AU2018248576A priority patent/AU2018248576B2/en
Priority to PL18713708T priority patent/PL3607014T3/pl
Priority to CN201880022980.1A priority patent/CN110494517B/zh
Priority to US16/498,219 priority patent/US11459478B2/en
Priority to RU2019134843A priority patent/RU2796008C2/ru
Priority to EP18713708.8A priority patent/EP3607014B1/fr
Priority to MX2019011382A priority patent/MX392151B/es
Publication of WO2018185094A1 publication Critical patent/WO2018185094A1/fr

Links

Classifications

    • 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
    • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • 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
    • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • 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
    • C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00

Definitions

  • the present disclosure relates to coating compositions comprising a hydroxyphenyl functional polymer, a latex polymer, a cross linker, and optionally one or more solvents, a dispersant, a lubricant and/or one or more pigments, methods of preparing the foregoing compositions, methods of preparing substrates coated with the foregoing compositions, and substrates coated with the foregoing compositions, particularly metal substrates.
  • Coating compositions are used on the surface of food and beverage packaging substrates to protect the contents of the packaging from, for example, contamination of the food or beverage due to corrosion of the packaging by its contents. Care must also be taken to avoid the loss of flavor from the food or beverage into the substrate.
  • the loss of flavor from the food or beverage into the substrate known as flavor scalping, arises from the migration of volatile flavorants in the packaged food or beverage into the coating on the surface of the packaging substrate.
  • Coating compositions formed from epoxy resins have been used to coat packaging and containers for foods and beverages. Although the weight of scientific evidence as interpreted by the major global regulatory food safety agencies in the US, Canada, Europe, and Japan, shows that the levels of bisphenol A (BPA) consumers are exposed to with current commercial epoxy based coatings is safe, there is nonetheless consumer concern over the possible migration of BPA into the food or beverage, making coatings that do not contain BPA or any other endocrine disruptors preferred.
  • BPA bisphenol A
  • coating compositions comprising a hydroxyphenyl functional polymer and a latex polymer impart favorable flavor scalping properties, while avoiding materials that are disfavorable to consumers. Accordingly, the present disclosure provides a coating composition comprising a hydroxyphenyl functional polymer, a latex polymer, crosslinker, and optionally one or more solvents, a dispersant, a lubricant and/or one or more pigments.
  • the present disclosure provides an alternative to epoxy based coatings that is substantially free of formaldehyde, bisphenols, isocyanates, phthalates, and organotins.
  • the coating compositions disclosed herein preferably do not contain, or are substantially free, of bisphenol A or other bisphenols.
  • the present disclosure also provides a coating composition comprising a hydroxyphenyl functional polymer and a latex polymer, wherein when the coating composition is applied onto a substrate to form a coating layer, the hydroxyphenyl functional polymer is not homogenously dispersed throughout the coating layer.
  • the present disclosure also provides methods of preparing the foregoing compositions. Also provided are methods of preparing substrates coated with the foregoing compositions, and substrates coated with the foregoing compositions, particularly metal substrates.
  • the coating compositions of the disclosure are useful for a variety of applications, including but not limited to coatings for food and beverage packaging and for metal packaging such as aerosol cans, paint cans, and industrial drums.
  • Figure 1 shows the TOF-SIMS depth profile results of BPANI A1 coated surfaces.
  • Figure 2 shows the TOF-SIMS depth profile results of CC-04 coated surfaces.
  • Figure 3 shows a comparison of TOF-SIMS depth profile results of Epoxy, BPANI A1 , and
  • the present disclosure provides a coating composition with the surprising benefit of favorable flavor scalping properties without the use of bisphenols and other materials that are disfavorable to consumers.
  • the compositions of the present disclosure comprise a hydroxyphenyl functional polymer, a latex polymer, a crosslinker, and optionally one or more solvents, a dispersant, a lubricant and/or one or more pigments.
  • the present disclosure provides a coated substrate comprising at least a layer of the coating composition.
  • the present disclosure provides a method of preparing a coated substrate comprising applying and curing a layer of the composition onto the surface of a substrate.
  • hydroxyphenyl functional polymer any polymer comprising phenolic groups.
  • the term “hydroxyphenyl functional polymer” also encompasses polymers comprising functionalized phenolic groups.
  • the hydroxyphenyl functional polymer may be a homopolymer or a copolymer.
  • the hydroxyphenyl functional polymer used in the compositions of the disclosure may be a single polymer type or a combination of two or more polymer types. In one approach, the hydroxyphenyl functional polymer of the coating composition does not comprise a phenol formaldehyde resole.
  • the hydroxyphenyl functional polymer may be functionalized with one or more functional groups.
  • exemplary functional groups include: acetal, acrylate, methacrylate, aldehyde, alkyl, alkoxy, amide, aryl, carbamate, carboxylate, halogen, hydroxyalkyl, hydroxyalkyl amide, oxazoline, azlactone, hydroxyl, isocyanate, ketone, methacrylate, nitrile, nitro, sulfide, sulfone, thiol, urethane, alkylvinyl, and vinyl.
  • the hydroxyphenyl functional polymer may be a catechol functional polymer, a
  • Novolac such as a Novolac phenolic resin, a hydroxyphenyl functional polymer with a Novolac-like structure, a poly(hydroxyphenol) compound, or a polyphenol.
  • the hydroxyphenyl functional polymer is poly(hydroxystyrene).
  • the poly(hydroxystyrene) can be linear or it can be branched.
  • Linear poly(hydroxystyrene) can for example be obtained by free radical polymerization of hydroxystyrene or its derivative(s).
  • Branched poly(hydroxystyrene) can also be obtained by free radical polymerization from hydroxystyrene or its derivative(s) but also via cationic polymerization.
  • Preferred hydroxystyrene monomer is 4-hydroxystyrene, also known as 4- vinylphenol.
  • the poly(hydroxystyrene) may comprise linear and/or branched poly(hydroxystyrene).
  • the poly (hydroxystyrene) can be a physical blend of linear poly(hydroxystyrene) and branched poly (hydroxystyrene), whereas in other embodiments the poly(hydroxystyrene) can be a polymeric structure comprising both linear and branched poly(hydroxystyrene).
  • the poly(hydroxystyrene) has a Novolac-like structure. Suitable poly(hydroxystyrene)s are for example disclosed in EP1756191 B1 .
  • the branched polyhydroxystyrene is a homopolymer of 4- hydroxyphenylmethylcarbinol.
  • the polymer of 4-hydroxyphenylmethylcarbinol contains branched moieties as illustrated below.
  • Such a polyhydroxystyrene oligomer has a Novolak type structure even though it is not produced from formaldehyde.
  • Exemplary poly(hydroxystyrene) polymers that can be used to prepare the coating compositions of the disclosure include PB5 (Hydrite Chemical Co. Brookfield Wl), solutions of poly(hydroxystyrene) in any alcohol, for example methanol, ethanol, butanol, propanol, and isopropanol, and PB5W (Hydrite Chemical Co., Brookfield, Wl).
  • Poly(hydroxystyrene) polymers may be obtained commercially, or may be prepared by methods known in the art (see, e.g., U.S. Patent Nos. 5,554,719 and 7,566,752).
  • the hydroxyphenyl functional polymer may have a number average molecular weight (M n ) as measured by GPC of 300 Da, 500 Da, 700 Da, 900 Da, 1000 Da, 1200 Da, 1400 Da, 1600 Da, 1800 Da, 2000 Da, 2200 Da, 2400 Da, 2600 Da, 2800 Da, 3000 Da, 3200 Da, 3400 Da, 3600 Da, 3800 Da, 4000 Da, 4200 Da, 4400 Da, 4600 Da, 4800 Da, or 5000 Da.
  • M n number average molecular weight as measured by GPC of 300 Da, 500 Da, 700 Da, 900 Da, 1000 Da, 1200 Da, 1400 Da, 1600 Da, 1800 Da, 2000 Da, 2200 Da, 2400 Da, 2600 Da, 2800 Da, 3000 Da, 3200 Da, 3400 Da, 3600 Da, 3800 Da, 4000 Da, 4200 Da, 4400 Da, 4600 Da, 4800 Da, or 5000 Da.
  • M n number average molecular weight
  • the M n of the hydroxyphenyl functional polymer may be 1000 Da, or greater, such as1000 - 5000 Da.
  • the hydroxyphenyl functional polymer may have an M n of 500-3000 Da, of 1000 - 3000 Da, of 2000 - 4000 Da, of 2000 - 3000 Da, of 2200 - 2800 Da, or of 2400 - 2800 Da, etc.
  • the Mn is greater than about 2000 Da., such as greater than 2500 Da.
  • 15% or less, 14% or less, 13% or less, 12% or less, 1 1 % or less, 10% or less, 9% or less, 8% or less, or 7% or less of the hydroxyphenyl functional polymer has a molecular weight of less than 1000 Da.
  • the hydroxyphenyl functional polymer may have a polydispersity from about 1 up to about 3, from about 1 up to about 2.5, or from about 1 up to about 2.
  • the hydroxyphenyl functional polymer may be present in the coating compositions of the disclosure in 0.1 %, 0.5%, 1 %, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, or 10% by weight of the coating compositions, or ranges between any two of these values.
  • the hydroxyphenyl functional polymer may be present in the coating compositions in 0.1 %- 10% by weight, in 1 %-10% by weight of the coating composition, in 2% - 8% by weight, in 1 % - 5% by weight, in 1 % - 3% by weight, or in 1 % - 2% by weight of the coating composition.
  • the latex polymer used in the coating compositions disclosed herein may be a homopolymer or it may be a copolymer.
  • the latex polymer used in the compositions of the disclosure may also be a single homopolymer, a single copolymer, a mixture of two or more homopolymers, a mixture of two or more copolymers, or a mixture of one or more homopolymers with one or more copolymers.
  • the latex polymer means herein a polymer capable of forming an aqueous dispersion (latex).
  • the polymer used in the present disclosure is preferably an addition polymer formed from ethylenically unsaturated monomers.
  • the latex polymer is (meth)acrylic or a styrene (meth)acrylic latex polymer.
  • the polymer is a (meth)acrylic polymer.
  • the (meth)acrylic polymer is preferably formed from the following monomers:
  • acrylic and methacrylic acid and esters thereof including, but not limited to, acrylic acid, methacrylic acid (MAA), methyl methacrylate (MMA), butyl acrylate (BA), hydroxypropyl methacrylate (HPMA), allyl methacrylate (AMA), ethylene glycol dimethylacrylate
  • MAA methacrylic acid
  • MMA methyl methacrylate
  • BA butyl acrylate
  • HPMA hydroxypropyl methacrylate
  • AMA allyl methacrylate
  • ELDMA cyclohexyl methacrylate
  • CHMA cyclohexyl methacrylate
  • nBMA n-butyl methacrylate
  • GMA glycidyl methacrylate
  • BMA benzyl methacrylate
  • BDDMA 1 ,3-butanediol dimethacrylate
  • GDMA glycerol dimethacrylate
  • IBOMA isobornyl methacrylate
  • polymers in the form of an aqueous dispersion (latex), wherein polymers are made by emulsion polymerisation.
  • aqueous dispersion latex
  • polymers are made by emulsion polymerisation.
  • a process involves the addition polymerisation of substantially water immiscible ethylenically unsaturated monomers using a water soluble polymerisation initiator in water.
  • polymerisation takes place in the water phase producing substantially water insoluble polymer which, as polymerisation proceeds, increases in molecular weight until it becomes completely insoluble in the water and consequently precipitates to form a particle.
  • the latex polymer is used in the form of a nanogel latex.
  • nanogel latexes are described in, e.g., EP 1325088B1 and US 6,646,041 , the contents of which are incorporated herein by reference.
  • Nanogel latexes allow for highly water resistant, stable aqueous dispersions of addition polymer particles to be made without using surfactants. This is achieved by using stabilizing solution copolymers containing amounts of crosslinking species which are significantly higher than previously proposed.
  • a solution copolymer, such as an acrylic copolymer, when employed as the sole stabilizer, can serve as the replacement for the surfactant in an emulsion polymerization.
  • the latex is an aqueous dispersion comprising particles of an addition polymer of ethylenically unsaturated monomers; and a stabilizing solution copolymer comprising weak acid containing species and crosslinking species.
  • the nanogel latex comprises an acrylic copolymer, prepared via solution polymerization, which contain monomers which are completely insoluble in water and thus provides a route for the incorporation of such monomers into a latex. Since the methacrylic acid is only present in the nanogel component, and a non-ionic initiator is employed for the emulsion polymerization stage, the resulting latex should contain lower levels of low molecular weight solution polymer. This will reduce extractibles and may improve the blush resistance of the final lacquer. Typically, nanogels particle size range from 50-1 OOnm.
  • the combination of monomers and their relative amounts can be adjusted to form latex polymers with different properties, including glass transition temperature (Tg), to allow for modifications in flexibility, hardness, adhesion, particle size, blush resistance, lubrication bloom, abrasion resistance, etc. for different applications.
  • Tg glass transition temperature
  • the latex polymer of the coating composition disclosed herein has a Fox Tg less than 100°C, less than 90°C, less than 80°C, less than 70°C, less than 60°C, less than 50°C, less than 40°C, less than 30°C, less than 20°C, less than 10°C, less than 5°C, less than 0°C, less than -10°C, or less than - 20°C.
  • the latex polymer of the coating composition has a Fox Tg greater than -20°C, greater than -10°C, greater than 0°C, greater than 5°C, greater than 10°C, greater than 20°C, greater than 30°C, greater than 40°C, greater than 50°C, greater than 60°C, greater than 70°C, greater than 80°C, greater than 90°C, or greater than 100°C.
  • the latex polymer may also have a Tg within a range between any of the aforementioned values, e.g. a Tg between -20°C and 5°C, between 20°C and 60°C, between 10°C and 100°C, etc.
  • low Tg latexes such as those with Tg's of 50°C to -18°C and having Fox Tg 3.7°C or lower, and of the same monomer make up as the nanogel latex polymer, can be used in conjunction with a nanogel latex polymer to improve flexibility of the finished coating.
  • the latex polymer may be present in the coating compositions of the disclosure in 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, or 80%, by weight of the coating compositions, or ranges between any two of these values.
  • the latex polymer may be present in the coating compositions in 40%-70% by weight, in 40% - 50% by weight, in 60% - 70% by weight, in 45% - 65% by weight, or in 50% - 60% by weight of the coating composition.
  • Latex polymers may be prepared, and/or stabilized during polymerization by methods known to those of skill in the art.
  • the methods may include those taught and referenced in, e.g., US 9,394,456, US 9,181 ,448, and US 9,404,006, the contents of which are incorporated herein by reference.
  • the latex polymer may be neutralized.
  • the neutralizer may include, without limitation, ammonia, a tertiary amine, such as, for non-limiting example, dimethylethanolamine, 2-dimethylamino-2-methyl-1 -propanol, tributylamine, morpholine, diethanolamine, triethanolamine, monoethanolamine, sodium hydroxide, potassium hydroxide, lithium hydroxide, and the like, or a combination thereof.
  • the neutralizer is present in an amount from about 20 to 100% mole-to-mole of acid in the compound to be neutralized.
  • the latex polymers of the present disclosure may have a relatively homogeneous latex particle structure and/or an inhomogeneous latex particle structure.
  • the latex particle structure may be controlled by the polymerization processes, including for non-limiting example a multi-stage polymerization process.
  • Such particle structures are usually prepared by a series of consecutive emulsion polymerization sequences with different monomer types, where the second stage monomer is polymerized in the presence of seed latex particles.
  • the latex polymer used in the coating compositions disclosed herein acts as an adhesive component for binding of the coating compositions to the substrate, and to provide chemical resistance.
  • the latex polymer may be any material that imparts adhesive properties, chemical resistance, flexibility, and/or durability to the coating compositions of the disclosure and/or the substrates coated with the coating compositions of the disclosure.
  • the latex polymer may be used in combination with a silane to promote adhesion to the substrate.
  • the crosslinker used in the coating compositions disclosed herein in some embodiments may be a hydroxyalkylamide crosslinker.
  • the hydroxyalkylamide crosslinker helps improve corrosion resistance when the coating composition is used as a protective coating that contacts food or beverage.
  • the hydroxyalkylamide crosslinker may include, without limitation, a beta-hydroxyalkyl amide crosslinker, such as Primid® XL-552
  • the crosslinker may be an oxazoline crosslinker.
  • exemplary oxazoline crosslinkers include, but are not limited to, bisoxazolines.
  • crosslinkers that may be used in the coating compositions disclosed herein include phenolics and lignins.
  • crosslinker(s) may be used in combination.
  • the crosslinker(s) may be present in the coating compositions of the disclosure in 0.5%, 1 %, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, or 10%, by weight of the coating compositions, or ranges between any two of these values.
  • the crosslinker(s) may be present in the coating compositions in 1 %-10% by weight, in 2% - 8% by weight, in 2% - 5% by weight, in 1 % - 2% by weight, or in 3% - 4% by weight of the coating composition.
  • the coating compositions of the disclosure include a solvent.
  • solvent is used herein to refer to water and to organic solvents, alone or as a combination of two or more solvents. Additionally, as used herein, the term “in solution” means in water, in an organic solvent, in a combination of two or more organic solvents, or in a combination of water and one or more organic solvents.
  • Organic solvents may include without limitation xylene, benzene, ethyl benzene, toluene, alkoxy alkanols, methanol, ethanol, propanol, butanol, alkyl ethers of ethylene, alkyl ethers of propylene glycol, ethylene glycol monobutyl ether, ethylene glycol ethyl ether, diethylene glycol monobutyl ether, a ketone, an aromatic solvent, an ester solvent, a hydroxyl functional solvent, and combinations thereof.
  • the amount of the solvent in the coating compositions of the disclosure may be 0.5%, 1 %, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 1 1 %, 12%, 13%, 14%, or 15% by weight of the coating compositions, or ranges between any two of these values.
  • the solvent may be present in the coating compositions in 1 %-7% by weight, in 2% - 6% by weight, in 2% - 4% by weight, in 2% - 3% by weight, or in 3% - 4% by weight of the composition.
  • the coating compositions of the disclosure may also optionally include a dispersant.
  • the dispersant used in the coating compositions disclosed herein may be a solution acrylic dispersant.
  • Solution acrylics are also known as solvent acrylics and are well known in the art.
  • the solution acrylic dispersant serves to disperse into the water phase any component that does not readily disperse in water. In some instances, without the acrylic dispersant, the coating may separate into two distinct phases.
  • Dispersants also referred to as surfactants
  • dispersants can include a mixture of emulsifiers and solvents that break oil components into smaller droplets for incorporation throughout the water.
  • Dispersants that can be used include polymeric or oligomeric surfactant based dispersing agents.
  • the solution acrylic dispersant of Example 3 below can be used, for example.
  • Other solution acrylic dispersants useful in the coating compositions of the disclosure are known in the art and are commercially available (e.g., from LUBRIZOL®, Wickliffe, Ohio).
  • the dispersant may be a phosphate solution polymer, such as EXP2900.
  • the dispersant can be used in an amount of 0.0%, 0.5%, 1 %, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, or 10% by weight of the coating compositions, or ranges between any two of these values.
  • the dispersant may be present in the coating compositions in 0.0%-10% by weight, in 1 %-7% by weight, in 2% - 6% by weight, in 2% - 4% by weight, in 2% - 3% by weight, in 3% - 4% by weight, or in 3%-6% by weight of the coating composition.
  • the dispersant may be a solution acrylic dispersant optionally in combination with a silane.
  • silanes include without limitation AMEO (3-aminopropyltriethoxysilane), GLYMO (3-glycidyloxypropyltrimethoxysilane), VTEO (vinyltriethoxysilane), and VTMO (vinyltrimethoxysilane).
  • the coating compositions of the disclosure may also optionally include a lubricant to aid in the coating process.
  • Exemplary lubricants include Aquacer® 1547 and may be present in 0.00%, 0.01 %, 0.05%, 0.10%, 0.15%, 0.20%, 0.25%, 0.30%, 0.35%, 0.40%, 0.45%, 0.50%, 0.55%, 0.60%, 0.65%, 0.70%, 0.75%, 0.80%, 0.85%, 0.90%, 1 .00%, 1 .05%, 1.10%, 1 .15%, 1.20%, 1 .25%, 1.30%, 1 .35%, 1.40%, 1 .45%, 1.50%, 1 .55%,
  • the lubricant may be present in the coating compositions in 0.01 % - 1 .75% by weight, 0.15% - 1 .50% by weight, 0.15% - 1 .00% by weight, 0.50% - 1.50% by weight, 0.75% - 1 .25% by weight, or 0.50% - 1.25% by weight of the composition.
  • the coating compositions of the present disclosure may also include acrylic polymers which are miscible in solvent, and further described in Example 3 below.
  • the coating compositions of the disclosure may also optionally include one or more pigments.
  • the pigment may be zinc oxide, carbon black, or titanium dioxide.
  • the coating compositions can include conventional additives known to those skilled in the art, such as, without limitation, additives to control foam, promote adhesion, reduce equilibrium and dynamic surface tension, or to control rheology and surface lubricity.
  • additives to control foam such as, without limitation, additives to control foam, promote adhesion, reduce equilibrium and dynamic surface tension, or to control rheology and surface lubricity.
  • M amyl alcohol, amyl alcohol, Dowanol PM, water-based silicone free wetting agents, and silicone free and silicone containing defoamers may be used to reduce foaming of the finished coating during application to the substrate.
  • Solvent ratios may also be manipulated to reduce foaming.
  • Neutralizers such as triethanol amine, diethyl amine, dimethylethanol amine, and diethanol amine may be added. Amounts and types of additives can vary depending on desired coating application and performance and are routinely determinable by those skilled in the art.
  • the coating compositions of the present disclosure are substantially free of formaldehyde, bisphenols, isocyanates, phthalates, and organotins.
  • the coating compositions of the disclosure are substantially free of styrene.
  • substantially free means that there is no more than 1 .0 % by weight, preferably no more than 0.5% by weight, and more preferably no more than 0.1 % by weight of the compound, or structural units derived from the compound, present in the coating composition.
  • the coating compositions of the disclosure may be prepared by, e.g., emulsifying a latex polymer in an aqueous carrier and then dispersing a solution of neutralizer in water into the latex emulsion to form a first solution, dispersing a crosslinker in solution into the first solution to form a second solution, mixing together a hydroxyphenyl functional polymer in solution and optionally a dispersant to form a third solution, mixing the third solution into the second solution, and adding solvent to form the coating composition.
  • a solution of neutralizer in water into the latex emulsion to form a first solution
  • dispersing a crosslinker in solution into the first solution to form a second solution
  • mixing together a hydroxyphenyl functional polymer in solution and optionally a dispersant to form a third solution
  • mixing the third solution into the second solution and adding solvent to form the coating composition.
  • the viscosity of the coating composition may be adjusted, for example by use of 50% DMEA in Dl H 2 0.
  • the viscosity may be of any value; in certain aspects of the disclosure, the viscosity may be 30-70 cps.
  • the composition may be filtered in advance of placing into a container for storage or shipment.
  • the coating compositions of the disclosure may be used on a substrate to form a coating layer for a variety of applications.
  • substrate includes, without limitation, food and beverage packaging and metal packaging, including plastic bottles, cans, metal cans, such as aluminum cans, and specifically aluminum beverage cans, beer and beverage easy-open-ends, aerosol cans, paint cans, industrial drums, packaging, containers, receptacles, or any portions thereof.
  • substrate includes, for non-limiting example, "can ends,” which can be stamped from can end stock and used in the packaging of beverages.
  • a “coating layer” refers to a contiguous barrier film layer across a substrate.
  • the coating layer comprises a substrate surface, wherein the “substrate surface” is the surface of the coating layer in contact with the substrate, and an upper surface, wherein “upper surface” refers to the surface opposite of the substrate surface, i.e. the surface that will be in contact with the contents of the packaging.
  • the substrate surface is the portion of the coating layer in contact with the aluminum can
  • the upper surface is the portion of the coating layer in contact with the soda.
  • One or more coating compositions may be applied in addition to the coating composition of the present disclosure, for non-limiting example, a prime coat may be applied between the substrate and a coating composition of the present disclosure.
  • the coating compositions of the disclosure can be applied to substrates by conventional methods known in the coating industry, or in any manner known to those skilled in the art.
  • spraying, rolling, dipping, and flow coating application methods can be used for both clear and pigmented films.
  • the coating compositions are sprayed onto a substrate.
  • the coating compositions may contain, for non-limiting example, from about 10% to about 30% by weight of the polymeric solids relative to about 70% to about 90% water and/or other solvents.
  • the coating compositions may contain, for non-limiting example, from about 20% to about 60% by weight of the polymer solids.
  • Organic solvents may be utilized in some embodiments to facilitate spray or other application methods and such solvents may include, without limitation, n-butanol, 2-butoxy-ethanol-1 , xylene, toluene, and mixtures thereof. In some embodiments, n-butanol is used in combination with 2-butoxyethanol-1.
  • the coating compositions may be cured thermally at temperatures in the range from about 215°C to about 250°C, and alternatively higher for a time sufficient to effect complete curing as well as volatilizing any fugitive components.
  • the coating compositions may be applied in some embodiments at a rate in the range from about 0.5 to about 15 milligrams per square inch of polymer coating per square inch of exposed substrate surface. In some embodiments, the coating compositions may be applied at a thickness from about 1 to about 25 microns.
  • the coating compositions are applied in some embodiments at a rate in the range from about 1.5 to about 15 milligrams of polymer coating per square inch of exposed substrate surface.
  • Conventional packaging coating compositions are applied to metal at about 232°C to about 247°C.
  • Some of the coating compositions of the current disclosure achieve good results at about 230°C or below, such as at about 210°C or below. This decreased temperature provides an energy savings to the coater, and it may allow the use of different alloys, such as tin- plated steel used for easy-open-ends. This also allows for recycling the ends together with the can body.
  • the hydroxyphenyl functional polymer is not homogenously distributed throughout the coating layer.
  • there is a gradient of the hydroxyphenyl functional polymer throughout the coating layer with a greater amount of the hydroxyphenyl functional polymer at upper surface of the coating layer than at the substrate surface.
  • the coating layer comprises a first portion comprising the upper surface and a second portion comprising the substrate surface, whereby there is a greater proportion of the hydroxyphenyl functional polymer in the first portion of the coating layer than in the second portion, and whereby there is a greater proportion of the latex polymer in the second portion than in the first portion.
  • the coating compositions of the disclosure have unexpectedly been found to impart favorable flavor scalping properties.
  • the coating compositions of the disclosure have been found to have comparable, and in some cases better, flavor scalping properties than, e.g., traditional epoxy coatings.
  • the coating compositions of the disclosure serve as a barrier to migration of flavorants in the contents of the packaging to the coated packaging substrate.
  • Classes of flavorants include aldehydes, ketones, alcohols and acids.
  • Aldehyde flavorants include octanal, nonanal, and decanal.
  • the coating layer of a cured coating composition of the disclosure exhibits a lower 14-day absorption of one or more of a 1 ppm aqueous solution of octanal, a 1 ppm aqueous solution of nonanal, or a 1 ppm aqueous solution of decanal than a substantially similar coating layer of a cured coating that is substantially free of a hydroxyphenyl functional polymer.
  • a 1 kg batch of 55 wt % poly(hydroxystyrene) was prepared by placing 550g of 100% solids poly(hydroxystyrene) into a mixing vessel, to which a nitrogen blanket was applied. 183g Butyl Cellosolve and 267g Butanol was added to the mixing vessel. The mixture was heated to 1 16°C for 3 hours, after which time the mixture was decanted after a slight cool down so that the solution had better flow, but still warm. Poly(hydroxystyrene) supplied in methanol, in ⁇ pH3 water solution, in hydrous form, and in butanol may be used to prepare this dispersion.
  • a nitrogen blanket was applied to a mixing vessel.
  • the mixture was heated to 1 15°C.
  • a premix of 103.48g methacrylic acid (MAA), 155.21 g methyl methacrylate (MMA), 16.73g acrylic acid (90% in Dl H 2 0), 10.95g Lucidol damped/BP-75-W/Perkadox L-W75, and 50.67g BC was prepared in a separate premix vessel.
  • the premix was pumped into mixing vessel over a period of 150 minutes while maintaining the temperature at 1 15-1 18°C.
  • the premix vessel was rinsed with 24.57g butanol, which was pumped into the mixing vessel over 30 minutes. 1 .37g TRIGONOX 21 / TBPEH was added, followed by addition of 2.3g butanol, and held for 30 minutes. The addition of TRIGONOX and butanol was repeated. The batch was cooled to 95°C and 41.89g dimethyl ethyl amine (DMEA) was added, and held for 15 minutes. 387.81 g Dl H 2 0 was added over 30 minutes. NV should be 29-31 % via STM 151.05.01 .
  • tBPEH t-Butyl-Per-2- Ethylhexanoate
  • Nanogel acrylic/solution polymers having amounts of MMA, BA, HPMA, MAA, AMA as shown in Table 1 were prepared.
  • Table 1 shows exemplary nanogel acrylic/solution polymers prepared.
  • 91 .10g cyclohexyl methacrylate (CHMA), 91 .10g methyl methacrylate (MMA), 24.87g butyl acrylate (BA), 1 1 .18g glycidyl methacrylate (GMA), and 6.43g allyl methacrylate (AMA) was mixed and added to the flask, mixed for 20 minutes while maintaining temperature at 60°C. 71.33g DiH 2 0 was fed into the mixture over 10 minutes. 1.43g t-butyl
  • NV should be 31 -33% via STM 151.05.01.
  • a 90,000-120,000 molecular weight PVB was also used in combination with the nanogel acrylic/solution polymer at 5%, 15%, and 25% of the solution for use in the miniemulsion/nanogel latex of Example 5.
  • Ratios of CHMA, MMA, BA, AMA, and GMA were altered to change Tg to allow for improved scalping (increased hardness) or improved flexibility. For the same reasons the ratio of nanogel acrylic/solution polymer: miniemulsion/nanogel latex was altered. Some changes to the monomer levels were also made to improve the flow and reduce foaming. BDDMA, GDMA, and EGDMA were all used as replacements for AMA and/or GMA. BNM was used as a replacement for CHMA to change the hardness and environmental resistances of the coating. Degree of Neutralization (DoN) has been varied from the standard 25% down to the 15% in tests to determine the effect of this on particle size as well as for the effect of changed particle size on the finished blend and its performance.
  • DoN Degree of Neutralization
  • Table 2 shows exemplary miniemulsion/nanogel latex polymers prepared.
  • Table 3 shows exemplary coating compositions prepared and evaluated.
  • the flavor scalping performance of the coating compositions of the disclosure were analyzed.
  • concentration of three different aldehydes in solution was monitored when exposed to a beverage can coating.
  • a loss in concentration of one or more of these aldehydes suggests poor flavor scalping performance which could have a detrimental effect on the flavor of the beverage during storage.
  • aldehydes of interest are octanal, nonanal and decanal. It is thought that these compounds are representative of the flavors commonly found in soft drinks and therefore monitoring the loss of these in solution acts as an indicator of coating performance.
  • Sample analysis was performed by means of gas chromatography ion mobility spectroscopy (GC-IMS), which is able to measure compounds at low ppm levels while producing reproducible, reliable results.
  • Samples were placed in 20 mL headspace vials and warmed to 60°C to increase the volatiles in the headspace. The headspace of each sample was measured and the amount of aldehyde present was quantified. Further details are provided below.
  • Control cans for each coating tested were prepared by filling the beverage can with the aldehyde solutions, sealing the can using the can seamer and then opening the can and removing 1 mL of solution for analysis. These cans were not incubated. This was repeated for each coating variable. Both the control can and the original bottled solution were analyzed in triplicate to determine what losses, if any where observed from initial can filling. Calibration Series
  • a serial dilution of the three aldehyde solution using acidified water matrix as the diluent was performed to obtain 10mL of each: 1 .0, 0.8, 0.6, 0.5, 0.3, 0.2, 0.1 ppm in triplicate for calibration.
  • 1 mL of sample was pipetted into a 20 mL headspace vial and sealed with a gas tight screw cap prior to sample analysis.
  • compositions of the present disclosure were compared with Epoxy (Aqualure® 2000), BPANI A (Aqualure® G1 50)to assess differences in performance over a 14 day time period.
  • Beverage cans applied with these coating were filled with an aldehyde solution containing octanal, nonanal and decanal at 1 ppm respectively and incubated at 40°C for up to 14 days.
  • concentrations of the individual aldehydes were quantified by means of GC- IMS.
  • Table 5 Summary of the concentration of octanal in the aldehyde solution after incubation and aging.
  • the concentration of the octanal in the solution decreased over time with the percentage decrease from control can to day 14 indicated by an arrow.
  • Each different can coating experienced a loss in aldehyde concentration.
  • the epoxy coating is used as a control and indicates what is an acceptable loss.
  • Table 6 Summary of the concentration of nonanal in the aldehyde solution after incubation and aging. The concentration of the nonanal in the solution decreased over time with the percentage decrease from control can to day 14 indicated by an arrow. Each different can coating experienced a loss in aldehyde concentration. The epoxy coating is used as a control and indicates what is an acceptable loss.
  • Table 7 Summary of the concentration of decanal in the aldehyde solution after incubation and aging.
  • the concentration of the decanal in the solution decreased over time with the percentage decrease from control can to day 14 indicated by an arrow.
  • Each different can coating experienced a loss in aldehyde concentration.
  • the epoxy coating is used as a control and indicates what is an acceptable loss.
  • Table 8 Summary of the concentration of octanal in the aldehyde solution after incubation and aging.
  • the concentration of the octanal in the solution decreased over time with the percentage decrease from control can to day 14 indicated by an arrow.
  • Each different can coating experienced a loss in aldehyde concentration.
  • the epoxy coating is used as a control and indicates what is an acceptable loss. All values have been normalized to the epoxy control can.
  • Table 9 Summary of the concentration of nonanal in the aldehyde solution after incubation and aging. The concentration of the nonanal in the solution decreased over time with the percentage decrease from control can to day 14 indicated by an arrow. Each different can coating experienced a loss in aldehyde concentration. The epoxy coating is used as a control and indicates what is an acceptable loss. All values have been normalized to the epoxy control can.
  • Table 10 Summary of the concentration of decanal in the aldehyde solution after incubation and ageing. The concentration of the decanal in the solution decreased over time with the percentage decrease from control can to day 14 indicated by an arrow. Each different can coating (as indicated by different colors) experienced a loss in aldehyde concentration, the epoxy coating (red) is used as a control and indicates what is an acceptable loss. All values have been normalized to the epoxy control can.
  • TOF-SIMS Time-of-Flight Secondary Ion Mass Spectrometry
  • compositions of the disclosure when used as can coatings, along with that of epoxy coatings and other can coatings.
  • Coatings analyzed include Epoxy (Aqualure® 2000), BPANI A1 (Aqualure® G1 50), and CC-04, a coating composition of the disclosure (78.5 wt.% latex, 5 wt.% Primid, 5 wt.% Silane, and 7.5 wt.% poly(hydroxy styrene), prepared in accordance with the methods disclosed above).
  • Epoxy surface vs. bulk content was assessed.
  • the outer surface (i.e. upper surface) of the epoxy coating was found to be enriched with an aromatic hydrocarbon compound with a spectral resemblance to polystyrene (PS); there was no evidence of BPA surface enrichment.
  • Depth profiles indicated surface depletion of BPA and 1.5-2x surface enrichment of PS-type of compound.
  • the thickness of the modified outer layer is less than 60 nm (assuming total film thickness of 4 micron) and the bulk of the coating is
  • the chemical composition of bulk and surface is very similar for the mass region 150-270 amu (i.e. mass region where for epoxy coating some clear differences are present); the pattern points to PS type of species.
  • the surface was enriched in aliphatic species/fragments (C2H5+, C3H5+, C4H7+, C5H9+, C6H 1 1 +, C7H1 1 +) and O-containing species/fragments (C2H50+, C3H70+, C4H70+, C5H70+, C6H70+, C7H90+, C2H302+, C4H402+, C5H502+, C6H702+) .
  • the aromatic species has a homogeneous in-depth distribution, i.e. no surface enrichment was observed as was for epoxy.
  • Aliphatic and O-containing species were enriched at outer surface of BPANI A1 ( ⁇ 60 nm) and profiles in negative polarity confirm a flat profile for aromatic species.
  • CC-04 the outer surface was found to be enriched in a species closely related to polystyrene (highly aromatic polymer), i.e. PB5, which was similar to epoxy. There was a surface enrichment of aromatic/hydroxy-styrenic species with a factor 1.5-2 as compared to the bulk (depth profiles, both polarities). In negative polarity the number of specific fragments is less than in the positive polarity. For CC-04, the relative surface enrichment of aromatics is higher than for epoxy.
  • a thin surface layer ( ⁇ 60 nm) is present which is enriched in PS type of material and depleted in BPA. Further in-depth, the coating chemical composition is homogeneous. For BPANI A1 , there was no surface enrichment of aromatic species observed, but surface enrichment of an O-containing and aliphatic hydrocarbon compound. For CC-04, the outer surface of the film is 1.5-2 times enriched in PB5 as compared to the bulk; no full phase separation (stratification) between PB5 and the other compounds could be established.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

L'invention concerne des compositions de revêtement comprenant un polymère fonctionnel hydroxyphényle, un polymère de latex, un agent de réticulation, et un ou plusieurs solvants, et éventuellement un dispersant, un lubrifiant et/ou un ou plusieurs pigments. Dans certains modes de réalisation, les compositions peuvent être utilisées pour revêtir des substrats tels que des boîtes et d'autres emballages pour aliments et boissons. Les compositions de revêtement de l'invention présentent des propriétés de scalpage d'arôme favorables.
PCT/EP2018/058480 2017-04-07 2018-04-03 Compositions de revêtement contenant un polymère fonctionnel hydroxyphényle et un polymère de latex WO2018185094A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
CA3056987A CA3056987A1 (fr) 2017-04-07 2018-04-03 Compositions de revetement contenant un polymere fonctionnel hydroxyphenyle et un polymere de latex
ES18713708T ES2881620T3 (es) 2017-04-07 2018-04-03 Composiciones de revestimiento que contienen un polímero con funcionalidad hidroxifenilo y un polímero de látex
AU2018248576A AU2018248576B2 (en) 2017-04-07 2018-04-03 Coating compositions containing a hydroxyphenyl functional polymer and a latex polymer
PL18713708T PL3607014T3 (pl) 2017-04-07 2018-04-03 Kompozycje powłokowe zawierające hydroksyfenylowo funkcjonalny polimer oraz polimer lateksowy
CN201880022980.1A CN110494517B (zh) 2017-04-07 2018-04-03 包含羟基苯基官能聚合物和胶乳聚合物的涂料组合物
US16/498,219 US11459478B2 (en) 2017-04-07 2018-04-03 Coating compositions containing a hydropyphenyl functional polymer and a latex polymer
RU2019134843A RU2796008C2 (ru) 2017-04-07 2018-04-03 Композиции для покрытия, содержащие гидроксифенил-функциональный полимер и латексный полимер
EP18713708.8A EP3607014B1 (fr) 2017-04-07 2018-04-03 Compositions de revêtement contenant un polymère fonctionnel hydroxyphényle et un polymère de latex
MX2019011382A MX392151B (es) 2017-04-07 2018-04-03 Composiciones de recubrimiento que contienen un polimero funcional de hidroxifenilo.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201762483007P 2017-04-07 2017-04-07
US62/483,007 2017-04-07
EP17171373 2017-05-16
EP17171373.8 2017-05-16

Publications (1)

Publication Number Publication Date
WO2018185094A1 true WO2018185094A1 (fr) 2018-10-11

Family

ID=58765689

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2018/058480 WO2018185094A1 (fr) 2017-04-07 2018-04-03 Compositions de revêtement contenant un polymère fonctionnel hydroxyphényle et un polymère de latex

Country Status (1)

Country Link
WO (1) WO2018185094A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11602768B2 (en) 2016-10-19 2023-03-14 Swimc, Llc Acrylic polymers and compositions containing such polymers

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5139834A (en) * 1990-10-29 1992-08-18 The Dexter Corporation Metal container coated with a composition comprising an acrylic polymer latex, melamine formaldehyde resin and a phenol formaldehyde resin
US5554719A (en) 1995-06-16 1996-09-10 Hoechst Celanese Corporation Polyhydroxystyrene with a novolak type structure
US6646041B2 (en) 2001-09-25 2003-11-11 Imperial Chemical Industries Plc Aqueous dispersion of addition polymer particles
EP1325088B1 (fr) 2000-09-26 2007-03-07 Imperial Chemical Industries Plc. DISPERSION AQUEUSE DEs PARTICULES D'UN POLYMERE D'ADDITION
US7566752B2 (en) 2004-05-05 2009-07-28 Du Pont Electronic Polymers L.P. Epoxy resins or polyisocyanates reacted with derivatized novolak polyhydroxystyrene
WO2013098218A1 (fr) * 2011-12-28 2013-07-04 Akzo Nobel Coatings International B.V. Émulsions de latex à fonction acétoacétate durcies avec des résines phénoliques, et compositions de revêtement ainsi réalisées
US9181448B2 (en) 2010-12-29 2015-11-10 Akzo Nobel Coatings International B.V. Latex emulsions and coating compositions formed from latex emulsions
US20150344737A1 (en) * 2012-12-18 2015-12-03 Akzo Nobel Coatings International B.V. Lignin Based Coating Compositions
US20150376435A1 (en) * 2013-03-01 2015-12-31 Valspar Sourcing, Inc. Aqueous coating compositions including phenolic resin(s)
US20160024337A1 (en) * 2013-03-15 2016-01-28 Akzo Nobel Coatings International B.V. Coating Compositions Having Hydroxyl Phenyl Functional Polymers
US9394456B2 (en) 2009-02-24 2016-07-19 Akzo Nobel Coatings International B.V. Latex emulsions and coating compositions formed from latex emulsions
US9404006B2 (en) 2013-03-15 2016-08-02 Akzo Nobel Coatings International B.V. Hybrid water dispersions, (poly)ethylene (meth)acrylic acid copolymer composite latex emulsions, hybrid (poly)ethylene (meth)acrylic acid organosilane composite latex emulsions, and coating compositions formed therefrom
WO2016196190A1 (fr) * 2015-05-29 2016-12-08 Ppg Industries Ohio, Inc. Composition de revêtement durcissable et emballage revêtu de celle-ci

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5139834A (en) * 1990-10-29 1992-08-18 The Dexter Corporation Metal container coated with a composition comprising an acrylic polymer latex, melamine formaldehyde resin and a phenol formaldehyde resin
US5554719A (en) 1995-06-16 1996-09-10 Hoechst Celanese Corporation Polyhydroxystyrene with a novolak type structure
EP1325088B1 (fr) 2000-09-26 2007-03-07 Imperial Chemical Industries Plc. DISPERSION AQUEUSE DEs PARTICULES D'UN POLYMERE D'ADDITION
US6646041B2 (en) 2001-09-25 2003-11-11 Imperial Chemical Industries Plc Aqueous dispersion of addition polymer particles
US7566752B2 (en) 2004-05-05 2009-07-28 Du Pont Electronic Polymers L.P. Epoxy resins or polyisocyanates reacted with derivatized novolak polyhydroxystyrene
EP1756191B1 (fr) 2004-05-05 2012-09-19 DuPont Electronic Polymers L.P. Polyhydroxystyrènes dérivés avec une structure de type novolak et processus de préparation de ceux-ci
US9394456B2 (en) 2009-02-24 2016-07-19 Akzo Nobel Coatings International B.V. Latex emulsions and coating compositions formed from latex emulsions
US9181448B2 (en) 2010-12-29 2015-11-10 Akzo Nobel Coatings International B.V. Latex emulsions and coating compositions formed from latex emulsions
WO2013098218A1 (fr) * 2011-12-28 2013-07-04 Akzo Nobel Coatings International B.V. Émulsions de latex à fonction acétoacétate durcies avec des résines phénoliques, et compositions de revêtement ainsi réalisées
US20150344737A1 (en) * 2012-12-18 2015-12-03 Akzo Nobel Coatings International B.V. Lignin Based Coating Compositions
US20150376435A1 (en) * 2013-03-01 2015-12-31 Valspar Sourcing, Inc. Aqueous coating compositions including phenolic resin(s)
US20160024337A1 (en) * 2013-03-15 2016-01-28 Akzo Nobel Coatings International B.V. Coating Compositions Having Hydroxyl Phenyl Functional Polymers
US9404006B2 (en) 2013-03-15 2016-08-02 Akzo Nobel Coatings International B.V. Hybrid water dispersions, (poly)ethylene (meth)acrylic acid copolymer composite latex emulsions, hybrid (poly)ethylene (meth)acrylic acid organosilane composite latex emulsions, and coating compositions formed therefrom
WO2016196190A1 (fr) * 2015-05-29 2016-12-08 Ppg Industries Ohio, Inc. Composition de revêtement durcissable et emballage revêtu de celle-ci

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11602768B2 (en) 2016-10-19 2023-03-14 Swimc, Llc Acrylic polymers and compositions containing such polymers
US11717852B2 (en) 2016-10-19 2023-08-08 Swimc Llc Alkali-soluble resin additives and coating compositions including such additives

Similar Documents

Publication Publication Date Title
US9038849B2 (en) Coating compositions for food and beverage containers
EP2658933B1 (fr) Émulsions latex et compositions de revêtement formées à partir d'émulsions latex
CN107690456B (zh) 涂布有乳液聚合的胶乳聚合物的包装
JP5769880B2 (ja) 非水系コーティング剤用の消泡剤
RU2670753C1 (ru) Акриловые водные дисперсии для покрытия контейнеров
DE112018004899T5 (de) Mehrstufige, polymere latizes, diese latizes enthaltende beschichtungszusammensetzungen und damit beschichtete artikel
WO2017112837A1 (fr) Polymères de latex fabriqués à l'aide d'un tensioactif neutralisé par une base métallique et compositions de revêtement résistantes au voile contenant ces polymères
DE112018004897T5 (de) Mehrstufige, polymere latizes, diese latizes enthaltende beschichtungszusammensetzungen und damit beschichtete artikel
AU2018248576B2 (en) Coating compositions containing a hydroxyphenyl functional polymer and a latex polymer
WO2017194464A1 (fr) Composition de copolymère d'éthylène sans bisphénol a-acide (méth)acrylique destinée à des revêtements de boîtes métalliques
WO2018185094A1 (fr) Compositions de revêtement contenant un polymère fonctionnel hydroxyphényle et un polymère de latex
US20210230443A1 (en) Packaging coating containing water-dispersible acrylic block copolymer
RU2796008C2 (ru) Композиции для покрытия, содержащие гидроксифенил-функциональный полимер и латексный полимер
US10975258B2 (en) Bisphenol A-free ethylene (meth)acrylic acid copolymer composition for metal can coatings
JPH08302275A (ja) 水性樹脂分散体
WO2025056403A1 (fr) Composition de revêtement aqueuse comprenant un copolymère acrylique dispersé
WO2024211388A1 (fr) Résine phénolique de résol vinylique, compositions de revêtement formées à partir de celle-ci, articles et procédés de revêtement

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 18713708

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 3056987

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 2018248576

Country of ref document: AU

Date of ref document: 20180403

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2018713708

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2018713708

Country of ref document: EP

Effective date: 20191107

点击 这是indexloc提供的php浏览器服务，不要输入任何密码和下载