US20210206952A1 - Aqueous ethylene-vinyl alcohol copolymer dispersion and oxygen barrier multilayer film coated with said dispersion - Google Patents

Aqueous ethylene-vinyl alcohol copolymer dispersion and oxygen barrier multilayer film coated with said dispersion Download PDF

Info

Publication number
US20210206952A1
US20210206952A1 US17/059,549 US201917059549A US2021206952A1 US 20210206952 A1 US20210206952 A1 US 20210206952A1 US 201917059549 A US201917059549 A US 201917059549A US 2021206952 A1 US2021206952 A1 US 2021206952A1
Authority
US
United States
Prior art keywords
ethylene
vinyl alcohol
alcohol copolymer
aqueous dispersion
lacquer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US17/059,549
Other versions
US11041067B1 (en
Inventor
Paolo Vacca
Sergio Santoro
Marco Mudu
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.)
SAES Getters SpA
Original Assignee
SAES Getters SpA
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 SAES Getters SpA filed Critical SAES Getters SpA
Assigned to SAES GETTERS S.P.A. reassignment SAES GETTERS S.P.A. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MUDU, Marco, SANTORO, Sergio, VACCA, PAOLO
Application granted granted Critical
Publication of US11041067B1 publication Critical patent/US11041067B1/en
Publication of US20210206952A1 publication Critical patent/US20210206952A1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions of 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 an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/02Homopolymers or copolymers of unsaturated alcohols
    • C08L29/04Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/048Forming gas barrier coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/541Silicon-containing compounds containing oxygen
    • C08K5/5415Silicon-containing compounds containing oxygen containing at least one Si—O bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/22Expanded, porous or hollow particles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0853Vinylacetate
    • C08L23/0861Saponified vinylacetate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L5/00Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
    • C08L5/08Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D129/00Coating 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 an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
    • C09D129/02Homopolymers or copolymers of unsaturated alcohols
    • C09D129/04Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/70Additives characterised by shape, e.g. fibres, flakes or microspheres
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/24Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/724Permeability to gases, adsorption
    • B32B2307/7242Non-permeable
    • B32B2307/7244Oxygen barrier
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/732Dimensional properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00Containers; Receptacles
    • B32B2439/70Food packaging
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/002Physical properties
    • C08K2201/003Additives being defined by their diameter
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Definitions

  • the present invention relates to an aqueous dispersion of Ethylene-Vinyl Alcohol (commonly abbreviated as EVOH) copolymers suitable to be used as lacquer to coat flexible or rigid substrates, in order to achieve excellent oxygen barrier properties, with particular reference to satisfy the requirements in the field of food packaging.
  • EVOH Ethylene-Vinyl Alcohol
  • Ethylene vinyl alcohol is a formal copolymer of ethylene and vinyl alcohol, usually prepared by polymerization of ethylene and vinyl acetate and subsequent hydrolysis of the obtained ethylene-vinyl acetate (EVA).
  • EVOH copolymer is often defined by its ethylene content measured in mol % and, as a consequence, both high-ethylene EVOH and low-ethylene EVOH can be commercially available.
  • materials for plastic packages should possess various other characteristics such as mechanical strength, heat resistance, chemical resistance, transparency and flexibility.
  • Synthetic polymeric materials are widely used in the manufacturing of a variety of articles for food packaging, but there are specific polymers, such as ethylene-vinyl alcohol copolymer (EVOH), polyamide (PA), polyvinyl alcohol copolymer (PVOH) and polyvinyl chloride (PVC) which have conventionally been used for providing coatings or layers with oxygen barrier properties.
  • EVOH ethylene-vinyl alcohol copolymer
  • PA polyamide
  • PVOH polyvinyl alcohol copolymer
  • PVC polyvinyl chloride
  • EVOH is characterized by better oxygen barrier performance in dry condition, at 0% relative humidity (RH), and the most relevant issue concerning its use as barrier material is related to its moisture sensitivity. Indeed, the hydrophilic nature of EVOH leads to the absorption of significant amounts of water when directly exposed to high humidity conditions (typically higher than 60% RH), due to the action of moisture that swells the polymeric composition and partially melts its crystalline phase, with a consequent increase of the final oxygen permeability. Therefore, there is a strict connection to be considered between the performance of EVOH as a barrier in food packages and the processing and storage conditions to which the packages are exposed, especially when severe conditions of high moisture and/or high temperature are involved.
  • RH relative humidity
  • EP 2164898 describes a barrier film comprising a blend of a first polymeric component, with 21 to 30 mol % ethylene-vinyl alcohol copolymer content, in an amount comprised between 65 to 95% weight, based on the blend weight, and a secondary barrier component with a range of 41-50 mol % ethylene-vinyl alcohol copolymer, in an amount comprised between 5 to 35% weight.
  • the final barrier film is obtained through extrusion techniques, for example tubular cast coextrusion, tubular or flat cast extrusion, blown bubble extrusion (for monolayer films) or coextrusion (for multilayer films).
  • Extrusion processes anyway, require some characteristics of the materials to be used as, for example, melting temperature suitable for process temperatures, thermodynamic stability under high temperature processing conditions and standard atmosphere (oxidation/degradation risk), mechanical stability under compressive and shear stresses as well as limitations in additives or fillers selection due to the high temperature processing, that can limit their applicability in particular in the field of the bio-compatible packaging.
  • one of the most relevant steps is represented by the preparation of a water-based formulation containing EVOH suitable for the manufacture, for instance, of lacquer coatings.
  • lacquer normally denotes a liquid formulation adopted to produce a packaging coating, which requires suitable physical and chemical resistant properties in order to protect the packed product from any deterioration and to achieve technical effects such as substrate wetting, flexibility, adhesion promotion and lubricity for the manufacturing process.
  • JP 2001172443 discloses an aqueous composition
  • the first ethylene-vinyl alcohol copolymer is dispersed in water in the form of fine particles and then in an aqueous dispersion of the second ethylene-vinyl alcohol copolymer.
  • JP 2001172443 the EVOH with high ethylene content is considered the best performing system under high humidity conditions, therefore, starting from its use as main component, they secondly add EVOH with low ethylene content, in order to improve the processability (i.e. solvent compatibility) of the composition.
  • JP 2001172443 reports that the low-ethylene EVOH is in an amount comprised between 0.05 and 100 parts by weight based on 100 parts by weight of the first EVOH, therefore they disclose a composition in which the amount of the high-ethylene EVOH is always greater than or equal to the amount of the low-ethylene EVOH.
  • EP 1816159 discloses an aqueous ethylene-vinyl alcohol-based copolymer dispersion characterized by gas barrier performance, long-term storage stability and good film-forming properties.
  • EP 1816159 specifically uses an EVOH copolymer with an ethylene content of 15-65 mol % and a degree of saponification not lower than 80 mol %, a base-neutralized ethylene/ ⁇ , ⁇ -unsaturated carboxylic acid-based copolymer and a polyvinyl alcohol with a degree of saponification of 75-100 mol %, a degree of polymerization of 100-3500 and in a content of 0.5-100 parts by weight per 100 parts by weight of EVOH copolymer.
  • the directly resulting laminates show an oxygen permeability, measured under condition of 20° C. and 85% relative humidity, not higher than 0.286 fm/Pa ⁇ s, preferably not higher than 0.229 fm/Pa ⁇ s, when the coat layer thickness is 15 ⁇ m.
  • the present invention relates to an aqueous dispersion comprising a first ethylene-vinyl alcohol copolymer in the form of capsules with an ethylene content comprised between 24 and 38 mol % (high ethylene content) dispersed in a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 15 mol % (low ethylene content), characterized in that the weight ratio between said first ethylene-vinyl alcohol copolymer and said second ethylene-vinyl alcohol copolymer is comprised between 0.40 and 0.70.
  • the presently claimed composition is characterized by a lower amount of high-ethylene EVOH with respect to the low-ethylene EVOH, in particular in a weight ratio comprised between 0.40 and 0.70, since a higher amount of high-ethylene EVOH with respect to low-ethylene EVOH causes a decrease in the oxygen barrier performance at medium relative humidity below than 60% RH.
  • the claimed relative amounts of low-ethylene EVOH having an ethylene content lower than 15 mol %, allows to obtain a water-soluble system
  • the relative claimed amounts of EVOH with higher ethylene content i.e. with an ethylene content in the range of 24-38 mol %, allows to increase the stability in the presence of high humidity conditions.
  • the presently claimed ratio between the high- and the low-ethylene content polymers is inverted with respect to the prior art and, considering the purpose of using the present gas barrier in high humidity conditions, our invention reports better oxygen permeability performances, specifically characterized by oxygen permeability measures (OTR) at 20° C. and 80% RH lower than 10 [cc day ⁇ 1 m ⁇ 2 ], with respect to the values comprised between 10 to 15 [cc day ⁇ 1 m ⁇ 2 ] of JP 2001172443.
  • OTR oxygen permeability measures
  • capsule preparation routes such as spray drying, emulsification, nano-precipitation and supercritical fluid technologies.
  • spray drying processing has been adopted to produce high-ethylene EVOH capsules.
  • the obtained capsules of the final aqueous dispersion which preserve their crystallinity in a wet environment, are characterized by a particle size distribution with a Volume Mean Diameter comprised between 0.1 and 10.0 ⁇ m and the presence of an internal cavity for particles with a diameter larger than 1.0 ⁇ m.
  • Said Volume Mean Diameter can be defined as the volume weighted mean particle size of the sample measured by dry dispersion laser diffraction and calculated by using Fraunhofer theory.
  • the aqueous dispersion can optionally comprise an alcohol, as for example ethanol or iso-propanol, in an amount lower than 10% by weight, in order to improve the homogeneity of the coating.
  • an alcohol as for example ethanol or iso-propanol
  • the present dispersion can further comprise the addition of both active or passive fillers in an amount comprised between 0.1 and 7% by weight.
  • active fillers like zeolites, as for instance Linde Type A (LTA) zeolites
  • LTA Linde Type A
  • the addition of passive fillers like graphene, graphene oxide or zirconium phosphate can improve the oxygen barrier performance in dry conditions, i.e. 0% relative humidity, by decreasing the coefficient of diffusion of oxygen in the polymeric network.
  • Mechanical stability and adhesion of the coating can be improved by using some dispersing agents, like tetraethoxysilane (TEOS) at a concentration preferably comprised between 25 and 100% weight with respect to the EVOH amount, or fillers such as cellulose at a concentration preferably below 7% weight with respect to the EVOH amount can be added.
  • TEOS tetraethoxysilane
  • fillers such as cellulose at a concentration preferably below 7% weight with respect to the EVOH amount
  • additives as for example chitosan, preferably in an amount comprised between 0.5 and 5% by EVOH weight, can be added in order to improve the recycling compatibility of the coating.
  • a coated barrier laminate with reduced thickness can be obtained in order to preserve significant properties like transparency, haze level, adhesion to plastic substrate, processability, higher recycling compatibility, mechanical stability and reduced costs, while keeping high barrier performances.
  • a lacquer-coated barrier laminate comprising at least a substrate and at least a coating layer, characterized in that said coating layer comprises capsules of a first ethylene-vinyl alcohol copolymer with an ethylene content comprised between 24 and 38 mol %, and a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 10 mol %, said first and second copolymers being in a respective weight ratio comprised between 0.40 and 0.70, wherein said coating layer has a thickness comprised between 0.1 and 10.0 ⁇ m.
  • the dispersion can be obtained by casting using a spiral bar, the solvent is evaporated and the obtained coating submitted to a baking process at a temperature comprised between 80° C. and 150° C., preferably between 130° C. and 150° C.
  • Alternative preparation processes can be blading, spin coating, dip coating, gravure coating, 3-roll coating, slot die coating, needle dispensing, jet dispensing.
  • the obtained thin coated layer provides excellent OTR values, while maintaining excellent performances for the typical properties required in packaging applications like transmittance and haze values.
  • composition of the lacquer coating is also characterized by relevant performance as a barrier for CO 2 making it, and the respective laminate, suitable for the application of food packaging in controlled atmosphere.
  • the substrate of the laminate structure can be selected from a non-limiting group consisting of Polyethylene Terephthalate (PET), Polyamide (PA), Polyethylene Furanoate (PEF), Polyethylene (PE), Polypropylene (PP), Polybutylene Adipate Terephthalate (PBAT), Polybutylene Succinate (PBS), Polylactic Acid (PLA), Polyhydroxyalkanoates (PHA), starch blends, lignin cellulose blend and cellophane, having a thickness comprised between 8 and 150 ⁇ m.
  • PET Polyethylene Terephthalate
  • PA Polyamide
  • PEF Polyethylene Furanoate
  • PE Polyethylene
  • PE Polypropylene
  • PBAT Polybutylene Adipate Terephthalate
  • PBS Polybutylene Succinate
  • PBS Polylactic Acid
  • PHA Polyhydroxyalkanoates
  • starch blends lignin cellulose blend and cellophane, having a thickness comprised between 8 and 150 ⁇ m.
  • said lacquer-coated laminate can consist in a multilayer system further comprising an adhesive layer, as a polyurethane laminating adhesive, which can be positioned in contact with the coated layer, with the substrate or both of them.
  • the high-ethylene EVOH capsules have been prepared by adding the ethylene-vinyl alcohol copolymer to an hydroalcoholic solution kept under stirring (at 100 rpm and 80° C.). Following the solubilization of the polymer, the resulting formulation has been spray-dried, and if required has been further submitted to jet-milling treatment in order to obtain monodispersed capsules with a Volume Mean Diameter of 5 ⁇ m ( ⁇ 20%) and a D90 lower than 10 ⁇ m (where D90 is defined as the particle dimension at 90% of the cumulative particle size distribution).
  • the comparative samples 1, 2 and 3 have been prepared with the above-described method but using relative ratios between the EVOH copolymers outside the presently claimed range.
  • Comparative sample 4 has been prepared according to EP 1816159. Specifically, a first solution (A) has been prepared by the solubilization of acrylic acid and NaOH in H 2 O at 80° C. under stirring. For the second solution (B), the amount of EVOH 27 mol % has been solubilized in 2-propanol and H 2 O at 80° C. under stirring. Subsequently, the first solution (A) has been injected into the second one (B) and the resulting solution was cooled at 5° C. for 12 hours and then mixed with a solution based on low-ethylene EVOH (15 mol %) and subsequently casted.
  • Sample compositions A to H are in accordance with the present invention and the relative OTR values for unit of thickness (OTR/ ⁇ m) are much better compared with the values of Comparative samples 1, 2 and 3, characterized by a different ratio between the two EVOH components, as well as with Comparative sample 4 which was prepared according to EP 1816159.
  • tables 2 and 3 show the observed values of Transmittance, Haze and CO 2 permeation rates for some samples.
  • the CO 2 permeation rates were measured by exposing both surfaces of the sample at 50% RH (50% RH/50% RH) and then increasing the relative humidity on the lacquer-coated surface of the barrier laminate to a value of 80% RH (80% RH/50% RH).
  • the experimental data have shown the ability of the coating obtained according with the composition of the present invention to act also as a CO 2 barrier, in different humidity conditions, with better performance if compared to the prior art (Sample B versus Comparative sample 1).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Laminated Bodies (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)

Abstract

An aqueous dispersion of ethylene-vinyl alcohol copolymers suitable to be used as lacquer to realize a thin coating both for flexible or rigid substrates, characterized by excellent oxygen and carbon dioxide barrier performances especially under high humidity conditions. The dispersion comprises a first ethylene-vinyl alcohol copolymer in the form of capsules with an ethylene content comprised between 24 and 38 mol % and a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 15 mol %.

Description

  • The present invention relates to an aqueous dispersion of Ethylene-Vinyl Alcohol (commonly abbreviated as EVOH) copolymers suitable to be used as lacquer to coat flexible or rigid substrates, in order to achieve excellent oxygen barrier properties, with particular reference to satisfy the requirements in the field of food packaging.
  • Ethylene vinyl alcohol (EVOH) is a formal copolymer of ethylene and vinyl alcohol, usually prepared by polymerization of ethylene and vinyl acetate and subsequent hydrolysis of the obtained ethylene-vinyl acetate (EVA). EVOH copolymer is often defined by its ethylene content measured in mol % and, as a consequence, both high-ethylene EVOH and low-ethylene EVOH can be commercially available.
  • With regard to the application field of the present invention, it is well known that loss of quality foods, shelf life reduction and spoilage events can occur through oxidation phenomena when the oxygen, entered into the package, reacts with food-reactive components or promotes the growth of aerobic bacteria. Therefore, an important part of the recent research in the food packaging area has been focused on preparing polymer materials with low oxygen permeability (i.e. high barrier). As anticipated above, by limiting the oxygen transmission from the environment into an oxygen-sensitive food item or a pharmaceutical product, the quality of the product can be preserved, the shelf life can be increased with a consequent waste reduction and cost saving.
  • In addition to the high barrier requirement, materials for plastic packages should possess various other characteristics such as mechanical strength, heat resistance, chemical resistance, transparency and flexibility.
  • Synthetic polymeric materials are widely used in the manufacturing of a variety of articles for food packaging, but there are specific polymers, such as ethylene-vinyl alcohol copolymer (EVOH), polyamide (PA), polyvinyl alcohol copolymer (PVOH) and polyvinyl chloride (PVC) which have conventionally been used for providing coatings or layers with oxygen barrier properties.
  • EVOH is characterized by better oxygen barrier performance in dry condition, at 0% relative humidity (RH), and the most relevant issue concerning its use as barrier material is related to its moisture sensitivity. Indeed, the hydrophilic nature of EVOH leads to the absorption of significant amounts of water when directly exposed to high humidity conditions (typically higher than 60% RH), due to the action of moisture that swells the polymeric composition and partially melts its crystalline phase, with a consequent increase of the final oxygen permeability. Therefore, there is a strict connection to be considered between the performance of EVOH as a barrier in food packages and the processing and storage conditions to which the packages are exposed, especially when severe conditions of high moisture and/or high temperature are involved.
  • EP 2164898 describes a barrier film comprising a blend of a first polymeric component, with 21 to 30 mol % ethylene-vinyl alcohol copolymer content, in an amount comprised between 65 to 95% weight, based on the blend weight, and a secondary barrier component with a range of 41-50 mol % ethylene-vinyl alcohol copolymer, in an amount comprised between 5 to 35% weight.
  • It is important to notice that in the above European prior art document the final barrier film is obtained through extrusion techniques, for example tubular cast coextrusion, tubular or flat cast extrusion, blown bubble extrusion (for monolayer films) or coextrusion (for multilayer films). Extrusion processes, anyway, require some characteristics of the materials to be used as, for example, melting temperature suitable for process temperatures, thermodynamic stability under high temperature processing conditions and standard atmosphere (oxidation/degradation risk), mechanical stability under compressive and shear stresses as well as limitations in additives or fillers selection due to the high temperature processing, that can limit their applicability in particular in the field of the bio-compatible packaging.
  • Therefore, in order to achieve the above relevant features in packaging solutions, one of the most relevant steps is represented by the preparation of a water-based formulation containing EVOH suitable for the manufacture, for instance, of lacquer coatings.
  • In this field, the term lacquer normally denotes a liquid formulation adopted to produce a packaging coating, which requires suitable physical and chemical resistant properties in order to protect the packed product from any deterioration and to achieve technical effects such as substrate wetting, flexibility, adhesion promotion and lubricity for the manufacturing process.
  • In this regard, JP 2001172443 discloses an aqueous composition comprising an ethylene-vinyl alcohol copolymer having an ethylene content of 16 to 70 mol % (high ethylene content) and an ethylene-vinyl alcohol copolymer having an ethylene content of 2 to 15 mol % (low ethylene content). The first ethylene-vinyl alcohol copolymer is dispersed in water in the form of fine particles and then in an aqueous dispersion of the second ethylene-vinyl alcohol copolymer. In JP 2001172443 the EVOH with high ethylene content is considered the best performing system under high humidity conditions, therefore, starting from its use as main component, they secondly add EVOH with low ethylene content, in order to improve the processability (i.e. solvent compatibility) of the composition. Specifically, JP 2001172443 reports that the low-ethylene EVOH is in an amount comprised between 0.05 and 100 parts by weight based on 100 parts by weight of the first EVOH, therefore they disclose a composition in which the amount of the high-ethylene EVOH is always greater than or equal to the amount of the low-ethylene EVOH.
  • EP 1816159 discloses an aqueous ethylene-vinyl alcohol-based copolymer dispersion characterized by gas barrier performance, long-term storage stability and good film-forming properties. EP 1816159 specifically uses an EVOH copolymer with an ethylene content of 15-65 mol % and a degree of saponification not lower than 80 mol %, a base-neutralized ethylene/α,β-unsaturated carboxylic acid-based copolymer and a polyvinyl alcohol with a degree of saponification of 75-100 mol %, a degree of polymerization of 100-3500 and in a content of 0.5-100 parts by weight per 100 parts by weight of EVOH copolymer. The directly resulting laminates show an oxygen permeability, measured under condition of 20° C. and 85% relative humidity, not higher than 0.286 fm/Pa·s, preferably not higher than 0.229 fm/Pa·s, when the coat layer thickness is 15 μm.
  • It is an object of the present invention to provide an aqueous ethylene-vinyl alcohol-based copolymer dispersion which is excellent in film-forming properties and, while preserving all the advantages related to a film also with a reduced thickness below 10 μm, is characterized by high gas barrier performance.
  • Specifically, the present invention relates to an aqueous dispersion comprising a first ethylene-vinyl alcohol copolymer in the form of capsules with an ethylene content comprised between 24 and 38 mol % (high ethylene content) dispersed in a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 15 mol % (low ethylene content), characterized in that the weight ratio between said first ethylene-vinyl alcohol copolymer and said second ethylene-vinyl alcohol copolymer is comprised between 0.40 and 0.70.
  • Considering the above-cited prior art documents, although also the present invention discloses the use of two types of EVOH, respectively characterized by low and high ethylene contents, it is evident that the final composition realized in the present invention is completely different and new.
  • If compared to the prior art, the presently claimed composition is characterized by a lower amount of high-ethylene EVOH with respect to the low-ethylene EVOH, in particular in a weight ratio comprised between 0.40 and 0.70, since a higher amount of high-ethylene EVOH with respect to low-ethylene EVOH causes a decrease in the oxygen barrier performance at medium relative humidity below than 60% RH. Moreover, the claimed relative amounts of low-ethylene EVOH, having an ethylene content lower than 15 mol %, allows to obtain a water-soluble system, whereas the relative claimed amounts of EVOH with higher ethylene content, i.e. with an ethylene content in the range of 24-38 mol %, allows to increase the stability in the presence of high humidity conditions.
  • More specifically, the presently claimed ratio between the high- and the low-ethylene content polymers is inverted with respect to the prior art and, considering the purpose of using the present gas barrier in high humidity conditions, our invention reports better oxygen permeability performances, specifically characterized by oxygen permeability measures (OTR) at 20° C. and 80% RH lower than 10 [cc day−1 m−2], with respect to the values comprised between 10 to 15 [cc day−1 m−2] of JP 2001172443.
  • Moreover, the inventors discovered that, in order to improve the EVOH barrier properties through the stabilization of its crystalline form, some capsule preparation routes have been adopted, such as spray drying, emulsification, nano-precipitation and supercritical fluid technologies. In particular spray drying processing has been adopted to produce high-ethylene EVOH capsules. The obtained capsules of the final aqueous dispersion, which preserve their crystallinity in a wet environment, are characterized by a particle size distribution with a Volume Mean Diameter comprised between 0.1 and 10.0 μm and the presence of an internal cavity for particles with a diameter larger than 1.0 μm. Said Volume Mean Diameter (VIVID) can be defined as the volume weighted mean particle size of the sample measured by dry dispersion laser diffraction and calculated by using Fraunhofer theory.
  • In some embodiments, the aqueous dispersion can optionally comprise an alcohol, as for example ethanol or iso-propanol, in an amount lower than 10% by weight, in order to improve the homogeneity of the coating.
  • Moreover, with the aim of improving the performance of the final barrier, the present dispersion can further comprise the addition of both active or passive fillers in an amount comprised between 0.1 and 7% by weight. In particular, the use of active fillers like zeolites, as for instance Linde Type A (LTA) zeolites, can improve the polymer performances in terms of moisture solubility inducing higher barrier performances under both low (below 60% RH) and high humidity conditions (80% RH). On the other hand, the addition of passive fillers like graphene, graphene oxide or zirconium phosphate can improve the oxygen barrier performance in dry conditions, i.e. 0% relative humidity, by decreasing the coefficient of diffusion of oxygen in the polymeric network.
  • Mechanical stability and adhesion of the coating can be improved by using some dispersing agents, like tetraethoxysilane (TEOS) at a concentration preferably comprised between 25 and 100% weight with respect to the EVOH amount, or fillers such as cellulose at a concentration preferably below 7% weight with respect to the EVOH amount can be added. Moreover, additives as for example chitosan, preferably in an amount comprised between 0.5 and 5% by EVOH weight, can be added in order to improve the recycling compatibility of the coating.
  • As second aspect achieved by the present invention, a coated barrier laminate with reduced thickness can be obtained in order to preserve significant properties like transparency, haze level, adhesion to plastic substrate, processability, higher recycling compatibility, mechanical stability and reduced costs, while keeping high barrier performances.
  • Indeed it is known, as reported in EP 1816159, that in order to reach high barrier performance, especially in high humidity condition, a higher thickness of the final film, usually higher than 10 μm, is required.
  • Nevertheless, in the present disclosure, the inventors have been able to prepare a lacquer-coated barrier laminate comprising at least a substrate and at least a coating layer, characterized in that said coating layer comprises capsules of a first ethylene-vinyl alcohol copolymer with an ethylene content comprised between 24 and 38 mol %, and a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 10 mol %, said first and second copolymers being in a respective weight ratio comprised between 0.40 and 0.70, wherein said coating layer has a thickness comprised between 0.1 and 10.0 μm.
  • For the preparation of the lacquer-coated barrier laminate characterized by low thickness values, the dispersion can be obtained by casting using a spiral bar, the solvent is evaporated and the obtained coating submitted to a baking process at a temperature comprised between 80° C. and 150° C., preferably between 130° C. and 150° C. Alternative preparation processes can be blading, spin coating, dip coating, gravure coating, 3-roll coating, slot die coating, needle dispensing, jet dispensing. The obtained thin coated layer provides excellent OTR values, while maintaining excellent performances for the typical properties required in packaging applications like transmittance and haze values.
  • Moreover the composition of the lacquer coating is also characterized by relevant performance as a barrier for CO2 making it, and the respective laminate, suitable for the application of food packaging in controlled atmosphere.
  • In some embodiments, the substrate of the laminate structure can be selected from a non-limiting group consisting of Polyethylene Terephthalate (PET), Polyamide (PA), Polyethylene Furanoate (PEF), Polyethylene (PE), Polypropylene (PP), Polybutylene Adipate Terephthalate (PBAT), Polybutylene Succinate (PBS), Polylactic Acid (PLA), Polyhydroxyalkanoates (PHA), starch blends, lignin cellulose blend and cellophane, having a thickness comprised between 8 and 150 μm.
  • In other possible embodiments, said lacquer-coated laminate can consist in a multilayer system further comprising an adhesive layer, as a polyurethane laminating adhesive, which can be positioned in contact with the coated layer, with the substrate or both of them.
  • Hereinafter, the invention will be explained in more detail with reference to the following examples.
  • According to the present invention, in Samples A-H the high-ethylene EVOH capsules have been prepared by adding the ethylene-vinyl alcohol copolymer to an hydroalcoholic solution kept under stirring (at 100 rpm and 80° C.). Following the solubilization of the polymer, the resulting formulation has been spray-dried, and if required has been further submitted to jet-milling treatment in order to obtain monodispersed capsules with a Volume Mean Diameter of 5 μm (±20%) and a D90 lower than 10 μm (where D90 is defined as the particle dimension at 90% of the cumulative particle size distribution). This formulation was then added to an aqueous formulation of the low-ethylene EVOH copolymer with an ethylene content lower than 15 mol %, in order to get the final aqueous dispersion with the aimed gas barrier properties. Finally, for the preparation of the lacquer-coated barrier laminate, the dispersion has been casted using a spiral bar, the solvent has been evaporated and the obtained coating submitted to a baking process at a temperature between 80° C. and 150° C.
  • The comparative samples 1, 2 and 3 have been prepared with the above-described method but using relative ratios between the EVOH copolymers outside the presently claimed range.
  • Comparative sample 4 has been prepared according to EP 1816159. Specifically, a first solution (A) has been prepared by the solubilization of acrylic acid and NaOH in H2O at 80° C. under stirring. For the second solution (B), the amount of EVOH 27 mol % has been solubilized in 2-propanol and H2O at 80° C. under stirring. Subsequently, the first solution (A) has been injected into the second one (B) and the resulting solution was cooled at 5° C. for 12 hours and then mixed with a solution based on low-ethylene EVOH (15 mol %) and subsequently casted.
  • TABLE 1
    List of Samples and Comparative Samples.
    high- low- high- OTR
    high- ethylene eth- ethylene/ (cm3 day−1
    ethylene EVOH ylene low- m−2)
    EVOH amount EVOH ethylene Thickness 80% RH, OTR/
    Sample (wt %) (mol %) (wt %) EVOH (μm) T = 23° C. μm
    A 30 27 70 0.43 5.0 2.4 0.5
    B 33 27 67 0.50 4.0 2.6 0.6
    C 33 32 67 0.50 7.0 4.3 0.6
    D 33 38 67 0.50 6.0 6.0 1
    E 35 27 65 0.54 5.0 4.2 0.8
    F 40 27 60 0.67 5.0 3.1 0.6
    G 33 27 67 0.50 10.0 1.4 0.1
    H 33 27 67 0.50 15.0 <1 0.07
    C1 0 27 100 0 5.0 65 13
    C2 25 27 75 0.33 5.0 30 6
    C3 100 27 0 5.0 >100 >20
    C4 4.06 27 2.64 1.54 4.0 10.5 2.6
  • Sample compositions A to H are in accordance with the present invention and the relative OTR values for unit of thickness (OTR/μm) are much better compared with the values of Comparative samples 1, 2 and 3, characterized by a different ratio between the two EVOH components, as well as with Comparative sample 4 which was prepared according to EP 1816159.
  • The obtained results for all the above samples and comparative samples (summarized in table 1), point out that a weight ratio between the high- and low-ethylene content EVOH outside the range claimed by the present invention, either lower than 0.4 or higher than 0.7, leads to oxygen permeability values not suitable for a film with a reduced thickness (i.e. lower than 10.0 μm) and high gas barrier requirements in high humidity conditions.
  • As representatives of the secondary technical effects that can be obtained by using compositions according to the present invention, tables 2 and 3 show the observed values of Transmittance, Haze and CO2 permeation rates for some samples.
  • TABLE 2
    Optical properties
    OTR
    Thickness [cc day−1 m−2] Transmittance Haze
    Sample [μm] 80% RH, T = 23° C. (%) (%)
    B  4.0 2.6 >90 49.2
    G 10.0 1.4 >90 82.8
    H 15.0 <1 >90 >80
  • The CO2 permeation rates were measured by exposing both surfaces of the sample at 50% RH (50% RH/50% RH) and then increasing the relative humidity on the lacquer-coated surface of the barrier laminate to a value of 80% RH (80% RH/50% RH).
  • In particular, the experimental data have shown the ability of the coating obtained according with the composition of the present invention to act also as a CO2 barrier, in different humidity conditions, with better performance if compared to the prior art (Sample B versus Comparative sample 1).
  • TABLE 3
    CO2 barrier properties
    high-ethylene
    EVOH/ CO2TR CO2TR
    low-ethylene [cc day−1 m−2] [cc day−1 m−2]
    Sample EVOH 50% RH, T = 23° C. 80% RH, T = 23° C.
    C1 0   26 500
    B 0.5  6  50

Claims (16)

1. An aqueous dispersion, comprising:
a first ethylene-vinyl alcohol copolymer in the form of capsules with an ethylene content ranging between 24 and 38 mol %; and
a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 15 mol %,
wherein a weight ratio between said first ethylene-vinyl alcohol copolymer and said second ethylene-vinyl alcohol copolymer is in a range of from 0.40 to 0.70.
2. The aqueous dispersion according to claim 1, wherein the first ethylene-vinyl alcohol copolymer in the form of capsules has an ethylene content ranging between 27 and 32 mol %.
3. The aqueous dispersion according to claim 1, further comprising:
an alcohol in an amount ranging between 5 and 10% by weight.
4. The aqueous dispersion according to claim 1, wherein the first ethylene-vinyl alcohol copolymer capsules have a particle size distribution with a volume mean diameter ranging between 0.1 and 10.0 μm.
5. The aqueous dispersion according to claim 4, wherein the first ethylene-vinyl alcohol copolymer capsules with a diameter larger than 1.0 μm comprise an internal cavity.
6. The aqueous dispersion according to claim 1, further comprising:
a filler in an amount ranging between 0.1 and 7% by weight.
7. The aqueous dispersion according to claim 6, wherein the filler is selected from the group consisting of zeolites, graphene, graphene oxide, cellulose, and zirconium phosphate.
8. The aqueous dispersion according to claim 1, further comprising:
tetraethoxysilane (TEOS) in an amount ranging between 25 and 100% by weight with respect to EVOH the first and second ethylene-vinyl alcohol copolymers.
9. The aqueous dispersion according to claim 1, further comprising:
chitosan in an amount ranging between 0.5 and 5% by weight with respect to the first and second ethylene-vinyl alcohol copolymers.
10. A lacquer-coated barrier laminate, comprising:
at least a substrate; and
at least a coating layer,
wherein said coating layer comprises a first ethylene-vinyl alcohol copolymer in the form of capsules with an ethylene content ranging between 24 and 38 mol %, and a second ethylene-vinyl alcohol copolymer with an ethylene content lower than 15 mol %, wherein a weight ratio between said first ethylene-vinyl alcohol copolymer and said second ethylene-vinyl alcohol copolymer is in a range of from 0.40 to 0.70.
11. The lacquer-coated barrier laminate according to claim 10, wherein the substrate is selected from the group consisting of polyethylene terephthalate (PET), polyamide (PA), polyethylene furanoate (PEF), polyethylene (PE), polypropylene (PP), polybutylene adipate terephthalate (PBAT), polybutylene succinate (PBS), polylactic acid (PLA), polyhydroxyalkanoates (PHA), starch blends, lignin cellulose blend, and cellophane.
12. The lacquer-coated barrier laminate according to claim 10, wherein the substrate has a thickness ranging between 8 and 150 μm.
13. The lacquer-coated barrier laminate according to claim 10, wherein the coating layer has a thickness ranging between 0.1 and 10.0 μm.
14. The lacquer-coated barrier laminate according to claim 10, further comprising:
an adhesive layer.
15. The lacquer-coated barrier laminate according to claim 14, wherein the coating layer is in contact with the adhesive layer.
16. The lacquer-coated barrier laminate according to claim 14, wherein the adhesive layer is a polyurethane laminating adhesive.
US17/059,549 2018-07-13 2019-07-11 Aqueous ethylene-vinyl alcohol copolymer dispersion and oxygen barrier multilayer film coated with said dispersion Active US11041067B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IT102018000007179 2018-07-13
IT102018000007179A IT201800007179A1 (en) 2018-07-13 2018-07-13 WATER DISPERSION OF ETHYLENE-VINYL ALCOHOL COPOLYMERS AND OXYGEN BARRIER MULTI-LAYER FILM COATED WITH THIS DISPERSION
PCT/IB2019/055909 WO2020012396A1 (en) 2018-07-13 2019-07-11 Aqueous ethylene-vinyl alcohol copolymer dispersion and oxygen barrier multilayer film coated with said dispersion

Publications (2)

Publication Number Publication Date
US11041067B1 US11041067B1 (en) 2021-06-22
US20210206952A1 true US20210206952A1 (en) 2021-07-08

Family

ID=63762885

Family Applications (1)

Application Number Title Priority Date Filing Date
US17/059,549 Active US11041067B1 (en) 2018-07-13 2019-07-11 Aqueous ethylene-vinyl alcohol copolymer dispersion and oxygen barrier multilayer film coated with said dispersion

Country Status (10)

Country Link
US (1) US11041067B1 (en)
EP (1) EP3797136B1 (en)
JP (1) JP7235775B2 (en)
KR (1) KR102418209B1 (en)
CN (1) CN112334531B (en)
BR (1) BR112021000541B1 (en)
ES (1) ES2905436T3 (en)
IT (1) IT201800007179A1 (en)
TW (1) TWI773908B (en)
WO (1) WO2020012396A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT202000005449A1 (en) * 2020-03-13 2021-09-13 Getters Spa Curing polymer compositions having improved oxygen barrier properties
IT202000018589A1 (en) 2020-07-30 2022-01-30 Getters Spa MULTILAYER FLEXIBLE PACKAGING WITH ANTIOXIDANT PROPERTIES
US20230159785A1 (en) * 2021-11-19 2023-05-25 E Ink California, Llc Sealing film compositions for sealing microcells of electro-optic devices
CN114808544B (en) * 2022-05-06 2023-07-14 山东金麦材料科技股份有限公司 High-barrier packaging paper and processing technology thereof
CN116080191B (en) * 2023-02-15 2024-10-08 浙江鹏远新材料科技集团股份有限公司 High-barrier packaging material and preparation method thereof

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6211644A (en) * 1985-06-26 1987-01-20 株式会社クラレ Laminate having excellent gas permeability resistance
JP3400128B2 (en) * 1994-08-30 2003-04-28 株式会社クラレ Aqueous composition and laminate
JP4077927B2 (en) * 1998-04-27 2008-04-23 住友化学株式会社 Resin composition and laminate
JP2000052501A (en) * 1998-06-03 2000-02-22 Kuraray Co Ltd Laminate and its manufacture
JP2001172443A (en) * 1999-12-15 2001-06-26 Kuraray Co Ltd Ethylene-vinyl alcohol copolymer water-based composition excellent in barrier property
US20020022144A1 (en) * 2000-05-19 2002-02-21 Hu Yang Enhanced oxygen barrier performance from modification of ethylene vinyl alcohol copolymers (EVOH)
ES2341724T3 (en) * 2004-11-25 2010-06-25 Sumitomo Seika Chemicals Co., Ltd. WATERPROOF DISPERSION OF ETHYLENE COPOLYMER / VINYL ALCOHOL.
US7834089B2 (en) * 2007-05-08 2010-11-16 E. I. Du Pont De Nemours And Company Ionomeric ethylene vinyl alcohol compositions
DK2164898T3 (en) 2007-06-11 2012-11-12 Cryovac Inc EVOH blend for improved oxygen resistance
JP6148669B2 (en) * 2012-06-13 2017-06-14 株式会社クラレ Ethylene-vinyl alcohol resin composition, multilayer sheet, packaging material and container
CN105073840A (en) * 2013-02-25 2015-11-18 巴斯夫欧洲公司 Particulate microcapsule composition
WO2015041135A1 (en) * 2013-09-20 2015-03-26 日本合成化学工業株式会社 Ethylene-vinyl alcohol copolymer composition and laminate and secondary molded article thereof using same
WO2015098772A1 (en) * 2013-12-27 2015-07-02 日本合成化学工業株式会社 Molding material comprising ethylene-vinyl ester copolymer saponification product
CN105131483A (en) * 2015-09-09 2015-12-09 沈阳化工大学 High-resistance co-mixing material with multilayer structure

Also Published As

Publication number Publication date
TWI773908B (en) 2022-08-11
US11041067B1 (en) 2021-06-22
CN112334531A (en) 2021-02-05
WO2020012396A1 (en) 2020-01-16
ES2905436T3 (en) 2022-04-08
KR102418209B1 (en) 2022-07-08
KR20210031864A (en) 2021-03-23
JP2021529844A (en) 2021-11-04
JP7235775B2 (en) 2023-03-08
EP3797136A1 (en) 2021-03-31
TW202006078A (en) 2020-02-01
IT201800007179A1 (en) 2020-01-13
BR112021000541B1 (en) 2023-03-14
EP3797136B1 (en) 2021-12-01
BR112021000541A2 (en) 2021-04-06
CN112334531B (en) 2021-09-14
BR112021000541A8 (en) 2023-01-10

Similar Documents

Publication Publication Date Title
US11041067B1 (en) Aqueous ethylene-vinyl alcohol copolymer dispersion and oxygen barrier multilayer film coated with said dispersion
JP6422932B2 (en) Packaging material, vacuum insulator, method for manufacturing packaging material, and method for manufacturing vacuum insulator
KR101209293B1 (en) Gas barrier transparent polymer composite films
CN114517049B (en) Coating liquid with high barrier property and application thereof
JP2017202624A (en) Gas barrier film
JP4864818B2 (en) Laminated film
JP2015516472A (en) Ionomer-poly (vinyl alcohol) blends and coatings
JP7470680B2 (en) Polymer-coated paper or paperboard
US9441132B2 (en) Methods for preparing highly viscous ionomer-poly(vinylalcohol) coatings
CA3069965C (en) High barrier oriented films
JP4586157B2 (en) Moisture-proof coating agent and moisture-proof processed product
JPH03112655A (en) Gas barrier multi-layered container and multi-layered package
CN105542272A (en) Polyethylene base film specially used for compounding with polyvinyl alcohol film and preparation method thereof
JP4168629B2 (en) Oxygen gas barrier film and method for producing the same
WO2024166930A1 (en) Resin composition, molded article, multilayer structure, and method for manufacturing resin composition
JP2022161306A (en) Gas-barrier film and package
AU2013226036A1 (en) High viscosity blends and coatings of an ionomer and poly(vinyl alcohol)
JP2016216596A (en) Polyamide film

Legal Events

Date Code Title Description
AS Assignment

Owner name: SAES GETTERS S.P.A., ITALY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:VACCA, PAOLO;SANTORO, SERGIO;MUDU, MARCO;REEL/FRAME:054487/0197

Effective date: 20190731

FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCF Information on status: patent grant

Free format text: PATENTED CASE