Multilayer base material, multilayer film provided with the multilayer base material, multilayer body provided with the multilayer film, and packaging material provided with the multilayer body

Abstract

To provide a base material having excellent interlayer adhesion with a vapor deposition film and having high gas barrier properties.SOLUTION: A multilayer base material according to the present invention is provided with at least a polypropylene resin layer and a coat layer. The polypropylene resin layer is stretched. The coat layer contains a resin material having a polar group.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] The present invention relates to a multilayer substrate, a multilayer film comprising the multilayer substrate, a laminate comprising the multilayer film, and the laminate.

[0002] Conventionally, films made of polyesters such as polyethylene terephthalate (hereinafter also referred to as polyester films) have been used as substrates for constituting laminates used in the production of packaging materials because they are excellent in mechanical properties, chemical stability, heat resistance, and transparency, as well as being inexpensive.

[0003] Depending on the contents to be filled into the packaging material, the packaging material may be required to have high gas barrier properties, such as oxygen barrier property and water vapor barrier property. To satisfy this requirement, it is common to form a vapor-deposited film containing alumina, silica, etc. on the surface of a polyester film (Patent Document 1).

[0004] In recent years, there has been a search for resin materials to replace polyester films, and the application of such materials to the substrate of polyolefin films, particularly polypropylene films, has been considered. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] Japanese Patent Application Publication No. 2005-053223 Summary of the Invention [Problem to be solved by the invention]

[0006] The inventors of the present invention were considering using a stretched polypropylene film (hereinafter also referred to as a stretched polypropylene film) instead of the conventional polyester film substrate, when they discovered a new problem that satisfactory gas barrier properties could not be obtained even when a vapor deposition film was formed on the surface of the stretched polypropylene film. As a result of further investigations, the inventors discovered that in packaging materials using a laminated film in which a vapor-deposited film is provided on the stretched polypropylene film, a unique phenomenon not seen in conventional laminated films using a polyester film base material occurs, namely, delamination occurs between the stretched polypropylene film and the vapor-deposited film, and they came to the knowledge that this phenomenon causes insufficient gas barrier properties.

[0007] The inventors then discovered that by providing a coating layer containing a resin material having a polar group on the surface of a stretched polypropylene film, the adhesion of the vapor-deposited film formed on the coating layer is improved and the gas barrier properties are also improved.

[0008] The present invention was made based on such findings, and the problem to be solved by the present invention is to provide a substrate having excellent interlayer adhesion with a vapor-deposited film and high gas barrier properties.

[0009] Another problem to be solved by the present invention is to provide a laminate film comprising the substrate. Another problem to be solved by the present invention is to provide a laminate comprising the laminate film. A further object of the present invention is to provide a packaging material comprising the laminate. [Means for solving the problem]

[0010] The multilayer substrate of the present invention is The multilayer substrate includes at least a polypropylene resin layer and a coating layer, The polypropylene resin layer is subjected to a stretching treatment, The coating layer is further characterized in that it contains a resin material having a polar group.

[0011] In one embodiment, the ratio of the thickness of the coating layer to the total thickness of the multilayer substrate is 1% or more and 20% or less.

[0012] In one embodiment, the coating layer has a thickness of 0.1 μm or more and 10 μm or less.

[0013] In one embodiment, the resin material is one or more resin materials selected from ethylene vinyl alcohol copolymer (EVOH), polyvinyl alcohol (PVA), polyester, polyethyleneimine, hydroxyl group-containing (meth)acrylic resin, nylon 6, nylon 6,6, MXD nylon, amorphous nylon, and polyurethane.

[0014] In one embodiment, the coating layer is a layer formed using a water-based emulsion or a solvent-based emulsion.

[0015] In one embodiment, the multi-layer substrate is used in packaging applications.

[0016] The laminated film of the present invention is characterized by comprising the above-mentioned multilayer substrate, a vapor-deposited film containing an inorganic oxide, and a vapor-deposited film on a coating layer.

[0017] In one embodiment, the inorganic oxide comprises silica or alumina.

[0018] In one embodiment, the laminate film of the present invention further comprises a barrier coat layer on the vapor-deposited film.

[0019] The laminate of the present invention is characterized by comprising the above laminate film and a sealant layer.

[0020] In one embodiment, the sealant layer is made of the same material as the polypropylene resin layer, which is polypropylene.

[0021] The packaging material of the present invention is characterized by comprising the above-mentioned laminate. Effect of the Invention

[0022] According to the present invention, it is possible to produce a packaging material having excellent interlayer adhesion between a polypropylene film and a vapor-deposited film and high laminate strength, and it is also possible to provide a substrate having high gas barrier properties. Furthermore, according to the present invention, a laminate film including the substrate can be provided. Furthermore, according to the present invention, a laminate comprising the laminate film can be provided. Furthermore, according to the present invention, a packaging material including the laminate can be provided. [Brief description of the drawings]

[0023] [Figure 1] FIG. 1 is a schematic cross-sectional view showing one embodiment of a multilayer base material of the present invention. [Diagram 2] 1 is a schematic cross-sectional view showing one embodiment of a laminated film of the present invention. [Diagram 3] 1 is a schematic cross-sectional view showing one embodiment of a laminated film of the present invention. [Figure 4] 1 is a schematic cross-sectional view showing one embodiment of a laminate of the present invention. [Diagram 5] FIG. 1 is a perspective view showing one embodiment of a packaging material of the present invention. [Figure 6] FIG. 1 is a perspective view showing one embodiment of a packaging material of the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0024] (Multilayer base material) As shown in FIG. 1, a multilayer substrate 10 of the present invention includes a polypropylene resin layer 11 and a coating layer 12.

[0025] Each layer of the multilayer container of the present invention will be described below.

[0026] (Polypropylene resin layer) The polypropylene resin layer is made of polypropylene and may have a single-layer structure or a multi-layer structure.

[0027] The polypropylene resin layer is a film that has been subjected to a stretching treatment, and the stretching treatment may be uniaxial stretching or biaxial stretching. The stretching ratio in the machine direction (MD direction) and the transverse direction (TD direction) of the polypropylene resin layer is preferably 2 times or more and 15 times or less, and more preferably 5 times or more and 13 times or less. By setting the stretching ratio at 2 times or more, the strength and heat resistance of the polypropylene resin layer can be further improved, and the printability of the polypropylene resin layer can be improved. From the viewpoint of the breaking limit of the polypropylene resin layer, the stretching ratio is preferably 15 times or less.

[0028] The polypropylene contained in the polypropylene resin layer may be any of a homopolymer, a random copolymer, and a block copolymer. A polypropylene homopolymer is a polymer of propylene alone, a polypropylene random copolymer is a random copolymer of propylene and an α-olefin other than propylene (e.g., ethylene, butene-1, 4-methyl-1-pentene, etc.), and a polypropylene block copolymer is a copolymer having a polymer block of propylene and a polymer block of the above-mentioned α-olefin other than propylene. Among these polypropylenes, it is preferable to use homopolymers or random copolymers from the viewpoint of transparency. When the rigidity and heat resistance of the packaging bag are important, it is preferable to use homopolymers, and when the impact resistance and the like are important, it is preferable to use random copolymers. It is also possible to use biomass-derived polypropylene and mechanically or chemically recycled polypropylene.

[0029] The polypropylene content in the polypropylene resin layer is preferably 70% by mass or more, more preferably 80% by mass or more, and even more preferably 90% by mass or more.

[0030] As long as the properties of the present invention are not impaired, the polypropylene resin layer may contain a resin material other than polypropylene, for example, polyolefins such as polyethylene, (meth)acrylic resins, vinyl resins, cellulose resins, polyamide resins, polyesters, and ionomer resins. Furthermore, within the scope of not impairing the characteristics of the present invention, the polypropylene resin layer may contain additives, such as crosslinking agents, antioxidants, antiblocking agents, slip agents, UV absorbers, light stabilizers, fillers, reinforcing agents, antistatic agents, pigments, and modifying resins.

[0031] The thickness of the polypropylene resin layer is preferably 10 μm or more and 50 μm or less, and more preferably 10 μm or more and 40 μm or less. By making the thickness of the polypropylene resin layer 10 μm or more, the strength and heat resistance of the multilayer base material can be further improved. Furthermore, by setting the thickness of the polypropylene resin layer to 50 μm or less, the film-forming property and processability of the multi-layered base material can be further improved.

[0032] The polypropylene resin layer may have a printed layer on its surface. The image formed on the printed layer is not particularly limited, and may be a letter, a pattern, a symbol, or a combination thereof. From the viewpoint of environmental impact, the formation of a printed layer on a substrate is preferably carried out using an ink derived from biomass. The method for forming the printed layer is not particularly limited, and examples of the method include conventionally known printing methods such as gravure printing, offset printing, flexographic printing, etc. Among these, flexographic printing is preferred from the viewpoint of environmental load.

[0033] The polypropylene resin layer may be subjected to a surface treatment, which can improve the adhesion to the coating layer. The method of surface treatment is not particularly limited, and examples thereof include physical treatments such as corona discharge treatment, ozone treatment, low-temperature plasma treatment using oxygen gas and / or nitrogen gas, and glow discharge treatment, as well as chemical treatments such as oxidation treatment using chemicals.

[0034] (Coat layer) The multilayer substrate of the present invention has a coating layer containing a resin material having a polar group on a polypropylene resin layer, and a vapor-deposited film having high adhesion can be formed on the coating layer, thereby improving the gas barrier properties. In addition, as described below, packaging materials produced using the multi-layer substrate of the present invention have high laminate strength.

[0035] The coating layer contains a resin material having a polar group. In the present invention, a polar group refers to a group containing one or more heteroatoms, and examples of the polar group include an ester group, an epoxy group, a hydroxyl group, an amino group, an amide group, a carboxyl group, a carbonyl group, a carboxylic anhydride group, a sulfone group, a thiol group, and a halogen group. Among these, from the viewpoint of lamination properties of the packaging material, a carboxyl group, a carbonyl group, an ester group, a hydroxyl group and an amino group are preferred, and a carboxyl group and a hydroxyl group are more preferred.

[0036] Preferred examples of resin materials having a polar group include ethylene-vinyl alcohol copolymers (EVOH), polyvinyl alcohol (PVA), polyester, polyethyleneimine, hydroxyl-containing (meth)acrylic resins, nylon 6, nylon 6,6, MXD nylon, amorphous nylon, and polyurethane, with hydroxyl-containing (meth)acrylic resins, ethylene-vinyl alcohol copolymers, and polyvinyl alcohol being particularly preferred. By using such a resin material, the adhesion of the evaporated film formed on the coating layer can be significantly improved, and the gas barrier properties of the film can be effectively improved.

[0037] In the present invention, the coating layer can be formed using an aqueous emulsion or a solvent-based emulsion. Specific examples of the aqueous emulsion include polyamide-based emulsion, polyethylene-based emulsion, and polyurethane-based emulsion, while specific examples of the solvent-based emulsion include polyester-based emulsion.

[0038] The content of the resin material having a polar group in the coating layer is preferably 70% by mass or more, more preferably 80% by mass or more, and even more preferably 90% by mass or more.

[0039] As long as the characteristics of the present invention are not impaired, the coating layer may contain a resin material other than the resin material having a polar group. Furthermore, within the scope of not impairing the characteristics of the present invention, the coating layer may contain additives, such as crosslinking agents, antioxidants, antiblocking agents, slip agents, UV absorbers, light stabilizers, fillers, reinforcing agents, antistatic agents, pigments, and modifying resins.

[0040] The ratio of the thickness of the coating layer to the total thickness of the multilayer substrate is preferably 1% or more and 20% or less, and more preferably 3% or more and 10% or less. By making the ratio of the thickness of the coating layer to the total thickness of the multilayer substrate 1% or more, the adhesion of the vapor-deposited film can be improved, the gas barrier properties can be improved, and the laminate strength of the packaging material can be improved. In addition, by setting the ratio of the thickness of the surface resin layer to the total thickness of the multilayer substrate to 20% or less, the processability of the multilayer substrate can be further improved. In addition, as described below, the recyclability of a packaging material produced using a laminate of the multilayer substrate of the present invention and a sealant layer made of polypropylene can be improved.

[0041] The thickness of the coating layer is preferably 0.1 μm or more and 10 μm or less, and more preferably 0.2 μm or more and 5 μm or less. By making the thickness of the coating layer 0.1 μm or more, the adhesion of the evaporated film can be improved, the gas barrier property can be improved, and the laminate strength of the packaging material can be improved. In addition, by setting the thickness of the coating layer to 10 μm or less, the processability of the multilayer substrate can be further improved. As described below, the recyclability of a packaging material produced using a laminate of the multilayer substrate of the present invention and a sealant layer made of polypropylene can be improved.

[0042] The multilayer substrate of the present invention can be produced offline. Specifically, a resin composition containing polypropylene is formed into a film using a T-die method, an inflation method, or the like, to form a resin film, which is then stretched, and a coating liquid for forming a coat is applied onto the resin film, followed by drying. The multilayer substrate of the present invention can also be produced in-line, specifically by forming a resin composition containing polypropylene into a film using a T-die method or an inflation method, etc., to form a resin film, stretching it in the machine direction (MD), applying a coating liquid for forming a coat onto the resin film, drying it, and then stretching it in the transverse direction (TD). Note that stretching in the transverse direction may be performed first.

[0043] (Laminated film) As shown in FIG. 3, the laminated film 20 of the present invention is characterized by comprising the above-mentioned multilayer substrate 10 and a vapor-deposited film 21 containing an inorganic oxide, in which the vapor-deposited film 21 is provided on a coating layer 12. In one embodiment, the laminate film 20 may further include a barrier coat layer 22 on the vapor-deposited film 21 as shown in FIG.

[0044] Hereinafter, each layer of the laminated film will be described. Note that the multi-layer base material has been described above, so a description thereof will be omitted here.

[0045] (evaporated film) The laminated film of the present invention has a vapor-deposited film containing an inorganic oxide on the coating layer. This can improve the gas barrier properties of the laminated film, specifically, the oxygen barrier properties and water vapor barrier properties. In addition, the weight loss of the contents filled in the packaging material produced using the laminated film of the present invention can be suppressed.

[0046] Examples of inorganic oxides include aluminum oxide (alumina), silicon oxide (silica), magnesium oxide, calcium oxide, zirconium oxide, titanium oxide, boron oxide, hafnium oxide, and barium oxide. Of the above, silica and alumina are preferred. Moreover, silica is particularly preferable because it does not require aging treatment after the deposition film is formed.

[0047] The thickness of the evaporated film is preferably 1 nm or more and 150 nm or less, more preferably 5 nm or more and 60 nm or less, and even more preferably 10 nm or more and 40 nm or less. By making the thickness of the vapor-deposited film 1 nm or more, the oxygen barrier property and water vapor barrier property of the laminate can be further improved. In addition, by making the thickness of the vapor-deposited film 150 nm or less, the occurrence of cracks in the vapor-deposited film can be prevented. Furthermore, as described below, the recyclability of a packaging material produced using a laminate of the laminated film of the present invention and a sealant layer made of polypropylene can be improved.

[0048] The deposition film can be formed by a conventional method, for example, physical vapor deposition methods (PVD methods) such as vacuum deposition, sputtering, and ion plating, and chemical vapor deposition methods (CVD methods) such as plasma chemical vapor deposition, thermal chemical vapor deposition, and photochemical vapor deposition.

[0049] Also, for example, a composite film consisting of two or more layers of vapor-deposited films of different inorganic oxides can be formed and used by combining both physical vapor deposition and chemical vapor deposition. The degree of vacuum in the vapor deposition chamber is 10 -2 ~10 -8 After oxygen is introduced, the pressure is preferably about 10 -1 ~10 -6 The pressure is preferably about mbar. The amount of oxygen introduced varies depending on the size of the deposition machine. For the oxygen to be introduced, an inert gas such as argon gas, helium gas, or nitrogen gas may be used as a carrier gas to the extent that no problems occur. The film transport speed can be about 10 to 800 m / min.

[0050] The surface of the deposited film is preferably subjected to the above-mentioned surface treatment, which can improve adhesion to adjacent layers.

[0051] (Barrier coat layer) The laminated film of the present invention may further include a barrier coat layer on the vapor-deposited film, which can improve the oxygen barrier property and water vapor barrier property of the laminated film.

[0052] In one embodiment, the barrier coat layer contains a gas barrier resin such as an ethylene-vinyl alcohol copolymer (EVOH), polyvinyl alcohol, polyacrylonitrile, polyamide such as nylon 6, nylon 6,6, and polymetaxylylene adipamide (MXD6), polyester, polyurethane, and (meth)acrylic resin. Among these, polyvinyl alcohol is preferred from the viewpoint of oxygen barrier property and water vapor barrier property. Furthermore, by including polyvinyl alcohol in the barrier coat layer, the occurrence of cracks in the vapor-deposited film can be effectively prevented.

[0053] The content of the gas barrier resin in the barrier coat layer is preferably 50% by mass or more and 95% by mass or less, and more preferably 75% by mass or more and 90% by mass or less. By making the content of the gas barrier resin in the barrier coat layer 50% by mass or more, the oxygen barrier property and water vapor barrier property of the substrate can be further improved.

[0054] The barrier coat layer may contain the above-mentioned additives to the extent that the characteristics of the present invention are not impaired.

[0055] The thickness of the barrier coat layer is preferably 0.01 μm or more and 10 μm or less, and more preferably 0.1 μm or more and 5 μm or less. By making the thickness of the barrier coat layer 0.01 μm or more, the oxygen barrier property and water vapor barrier property of the laminated film can be further improved. By making the thickness of the barrier coat layer 10 μm or less, the processability of the laminated film can be improved. In addition, the recyclability of the packaging material produced by using the laminate of the laminated film of the present invention and the sealant layer made of polypropylene can be improved.

[0056] The barrier coat layer can be formed by dissolving or dispersing the above-mentioned material in water or a suitable solvent, applying the solution, and drying the solution. Alternatively, the barrier coat layer can be formed by applying a commercially available barrier coat agent and drying the solution.

[0057] In another embodiment, the barrier coat layer is a gas barrier coating film containing at least one resin composition such as a hydrolysate of a metal alkoxide or a hydrolyzed condensate of a metal alkoxide obtained by polycondensing a mixture of a metal alkoxide and a water-soluble polymer by a sol-gel method in the presence of a sol-gel catalyst, water, an organic solvent, etc. By providing such a barrier coat layer on the vapor-deposited film, the occurrence of cracks in the vapor-deposited film can be effectively prevented.

[0058] In one embodiment, the metal alkoxide is represented by the following general formula: R 1 n M(OR 2 ) m (In the formula, R 1 , R 2 each represents an organic group having 1 to 8 carbon atoms, M represents a metal atom, n represents an integer of 0 or more, m represents an integer of 1 or more, and n+m represents the atomic valence of M.

[0059] As the metal atom M, for example, silicon, zirconium, titanium, aluminum, etc. can be used. Also, R 1 and R 2 Examples of the organic group represented by the formula (I) include alkyl groups such as a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, and an i-butyl group.

[0060] Examples of metal alkoxides that satisfy the above general formula include tetramethoxysilane (Si(OCH 3 ) 4 ), tetraethoxysilane (mass%) Si(OC 2 H 5 ) 4 ), tetrapropoxysilane (Si(OC 3 H 7 ) 4 ), tetrabutoxysilane (Si(OC 4 H 9 ) 4 ) etc.

[0061] It is also preferable to use a silane coupling agent together with the metal alkoxide. As the silane coupling agent, known organic reactive group-containing organoalkoxysilanes can be used, and in particular, organoalkoxysilanes having epoxy groups are preferred. As organoalkoxysilanes having epoxy groups, for example, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, and β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane can be mentioned.

[0062] Two or more of the above silane coupling agents may be used, and the silane coupling agent is preferably used in an amount within the range of about 1 to 20 parts by mass per 100 parts by mass of the total amount of the alkoxide.

[0063] As the water-soluble polymer, polyvinyl alcohol and an ethylene-vinyl alcohol copolymer are preferred, and from the viewpoints of oxygen barrier properties, water vapor barrier properties, water resistance and weather resistance, it is preferred to use these in combination.

[0064] The content of the water-soluble polymer in the gas barrier coating film is preferably 5 parts by mass or more and 500 parts by mass or less per 100 parts by mass of the metal alkoxide. By making the content of the water-soluble polymer in the gas barrier coating film 5 parts by mass or more per 100 parts by mass of the metal alkoxide, the oxygen barrier property and water vapor barrier property of the laminated film can be further improved. Also, by making the content of the water-soluble polymer in the gas barrier coating film 500 parts by mass or less per 100 parts by mass of the metal alkoxide, the film formability of the gas barrier coating film can be improved.

[0065] The thickness of the gas barrier coating film is preferably from 0.01 μm to 100 μm, and more preferably from 0.1 μm to 50 μm, which can improve the oxygen barrier property and water vapor barrier property while maintaining recyclability. By making the thickness of the gas barrier coating film 0.01 μm or more, the oxygen barrier property and water vapor barrier property of the laminated film can be improved, and the occurrence of cracks in the vapor deposition film can be prevented. By setting the thickness of the gas barrier coating film to 100 μm or less, the recyclability of a packaging material produced using a laminate of the laminate film of the present invention and a sealant layer made of polypropylene can be improved.

[0066] The gas barrier coating film can be formed by applying a composition containing the above-mentioned materials by a conventionally known means such as roll coating using a gravure roll coater or the like, spray coating, spin coating, dipping, brushing, bar coding, or an applicator, and then polycondensing the composition by a sol-gel method. As the sol-gel catalyst, an acid or an amine compound is preferable. As the amine compound, a tertiary amine that is substantially insoluble in water and soluble in an organic solvent is preferable, and examples thereof include N,N-dimethylbenzylamine, tripropylamine, tributylamine, and tripentylamine. Among these, N,N-dimethylbenzylamine is preferable. The sol-gel catalyst is preferably used in the range of 0.01 to 1.0 part by mass, and more preferably 0.03 to 0.3 part by mass, per 100 parts by mass of the metal alkoxide. By using a sol-gel catalyst in an amount of 0.01 part by mass or more per 100 parts by mass of the metal alkoxide, the catalytic effect can be improved, and by using a sol-gel catalyst in an amount of 1.0 part by mass or less per 100 parts by mass of the metal alkoxide, the thickness of the gas barrier coating film formed can be made uniform.

[0067] The composition may further contain an acid, which is used as a catalyst in the sol-gel process, mainly for the hydrolysis of alkoxides, silane coupling agents, and the like. The acid may be a mineral acid such as sulfuric acid, hydrochloric acid, or nitric acid, or an organic acid such as acetic acid, tartaric acid, etc. The amount of the acid used is preferably 0.001 mol or more and 0.05 mol or less based on the total molar amount of the alkoxide and the alkoxide portion (e.g., silicate portion) of the silane coupling agent. The amount of acid used is 0.001 moles or more relative to the total molar amount of the alkoxide and the alkoxide portion (e.g., silicate portion) of the silane coupling agent, thereby improving the catalytic effect. Also, the amount of acid used is 0.05 moles or less relative to the total molar amount of the alkoxide and the alkoxide portion (e.g., silicate portion) of the silane coupling agent, thereby making the thickness of the gas barrier coating film formed uniform.

[0068] The composition preferably contains water in an amount of 0.1 to 100 moles, more preferably 0.8 to 2 moles, per mole of the total molar amount of the alkoxides. By controlling the water content to 0.1 moles or more per mole of the total molar amount of the alkoxides, the oxygen barrier property and water vapor barrier property of the laminate of the present invention can be improved. Also, by controlling the water content to 100 moles or more per mole of the total molar amount of the alkoxides, the hydrolysis reaction can be carried out quickly.

[0069] The composition may also contain an organic solvent, such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, or n-butanol.

[0070] Hereinafter, one embodiment of the method for forming a gas barrier coating film will be described. First, a composition is prepared by mixing a metal alkoxide, a water-soluble polymer, a sol-gel catalyst, water, an organic solvent, and optionally a silane coupling agent, etc. In the composition, a polycondensation reaction gradually proceeds. Next, the composition is applied onto the vapor-deposited film by the above-mentioned conventionally known method and dried. This drying process further advances the polycondensation reaction between the alkoxide and the water-soluble polymer (and the silane coupling agent, if the composition contains a silane coupling agent) to form a composite polymer layer. Finally, the composition is heated at a temperature of 20 to 250° C., preferably 50 to 220° C., for 1 second to 10 minutes to form a gas barrier coating film.

[0071] The barrier coat layer may have a printed layer formed thereon. The method for forming the printed layer is as described above.

[0072] (Laminate) The laminate 30 of the present invention is characterized by comprising the laminate film 20 and a sealant layer 31, as shown in FIG.

[0073] Each layer of the laminate will be described below. Note that the laminate film has been described above, so a description thereof will be omitted here.

[0074] (Sealant layer) In one embodiment, the sealant layer may be formed of a resin material that can be fused to each other by heat, and examples of such materials include low density polyethylene (LDPE), medium density polyethylene (MDPE), high density polyethylene (HDPE), linear low density polyethylene (LLDPE), ethylene-α-olefin copolymers polymerized using a metallocene catalyst, random or block copolymers of ethylene and polypropylene, polypropylene, ethylene-vinyl acetate copolymer (EVA), ethylene-acrylic acid copolymer (EAA), ethylene-ethyl acrylate copolymer (EEA), ethylene-methacrylic acid copolymer (EMAA), ethylene, and the like. Examples of suitable resins include ethylene-methyl methacrylate copolymers (EMMA), ionomer resins, heat-sealable ethylene-vinyl alcohol resins, or copolymerized resins, polyolefins such as methylpentene resins, ethylene-propylene copolymers, methylpentene polymers, polybutene polymers, polyethylene, polypropylene, or cyclic olefin copolymers, acid-modified polyolefins obtained by modifying polyolefins with unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic acid, maleic anhydride, fumaric acid, and itaconic acid, polyesters such as PET, polyvinyl acetate resins, poly(meth)acrylic resins, and polyvinyl chloride resins. Conventionally, a laminate in which a substrate and a sealant layer are made of different resin materials has been used to produce a packaging material. However, since it is difficult to separate the substrate and the sealant layer after collecting the used packaging material, the current situation is that the laminate is not actively recycled. By forming the substrate and the sealant layer from the same material, it is not necessary to separate the substrate and the sealant layer, and therefore the recycling suitability can be improved. That is, from the viewpoint of the recyclability of the packaging material produced using the laminate, it is preferable that the sealant layer be made of polypropylene among the above-mentioned resin materials.

[0075] The sealant layer may contain the above-mentioned additives as long as the characteristics of the present invention are not impaired.

[0076] The sealant layer may have a single-layer structure or a multi-layer structure.

[0077] The thickness of the sealant layer is preferably 20 μm or more and 100 μm or less, and more preferably 30 μm or more and 70 μm or less. By making the thickness of the sealant layer 20 μm or more, the laminate strength of the packaging material including the laminate of the present invention can be further improved. Moreover, by setting the thickness of the sealant layer to 100 μm or less, the processability of the laminate of the present invention can be further improved.

[0078] (packaging material) The packaging material of the present invention is characterized by comprising the laminate. Examples of the packaging material include packaging products (packaging bags), lids, and laminate tubes.

[0079] Examples of packaging bags include packaging bags of various shapes, such as standing pouch type, side seal type, two-sided seal type, three-sided seal type, four-sided seal type, envelope seal type, grommet seal type (pillow seal type), pleated seal type, flat bottom seal type, square bottom seal type, and gusset type.

[0080] A standing pouch, which is an example of a packaging bag including the laminate of the present invention, will be described. Fig. 5 is a diagram showing a simplified example of the configuration of a standing pouch. As shown in Fig. 5, a standing pouch 40 is composed of a body portion (side sheet) 41 and a bottom portion (bottom sheet) 42. The side sheet 41 and bottom sheet 42 of the standing pouch 20 may be composed of the same material or different materials.

[0081] In one embodiment, the body 41 of the standing pouch 40 can be formed by bag making so that the heat seal layer of the laminate of the present invention becomes the innermost layer. In another embodiment, the side sheet 41 can be formed by preparing two sheets of the laminate of the present invention, overlapping them with their heat seal layers facing each other, inserting two sheets of laminate folded in a V shape into both ends of the overlapped laminate so that the heat seal layers are on the outside, and heat sealing them. According to this production method, a stand pouch having a body with a gusset 43 as shown in Fig. 6 can be obtained.

[0082] In one embodiment, the bottom sheet 22 of the standing pouch 20 can be formed by inserting the laminate of the present invention between pre-formed side sheets and heat sealing them. More specifically, the laminate can be formed by folding it into a V shape so that the heat seal layer is on the outside, inserting it between side sheets that have been made into a bag, and heat sealing it.

[0083] The heat sealing can be performed by a known method such as bar sealing, rotary roll sealing, belt sealing, impulse sealing, high frequency sealing, ultrasonic sealing, etc.

[0084] The contents filled in the packaging material are not particularly limited, and may be liquid, powder, or gel. In addition, the contents may be food or non-food. EXAMPLES

[0085] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to the following examples.

[0086] Example 1 A coating layer-forming solution having the following composition was applied to the corona-treated surface of a 20 μm-thick biaxially oriented polypropylene film (ME-1, manufactured by Mitsui Chemicals Tohcello Co., Ltd.) with one side corona-treated, and dried to form a coating layer with a thickness of 0.5 μm, thereby obtaining a multilayer substrate of the present invention. (Composition of coating solution for forming coating layer) Polyvinyl alcohol 5% by weight (Nippon Bismuth Poval Co., Ltd., VC-10, polymerization degree 1000, saponification degree 99.3 mol% or more) ·Water 90% by mass Isopropanol (IPA) 5% by weight

[0087] Example 2 A coating layer-forming solution having the following composition was applied to the corona-treated surface of the biaxially oriented polypropylene film and dried to form a coating layer having a thickness of 0.5 μm, thereby obtaining a multilayer substrate of the present invention. (Composition of coating solution for forming coating layer) ·EVOH 75% by mass (Eversolve #10, manufactured by Nippon Cima Co., Ltd.) ·Water 12.5% ​​by mass 1-Propanol 12.5% ​​by mass

[0088] Example 3 A coating layer-forming solution having the following composition was applied to the corona-treated surface of the biaxially oriented polypropylene film and dried to form a coating layer having a thickness of 0.5 μm, thereby obtaining a multilayer substrate of the present invention. (Composition of coating solution for forming coating layer) Polyester 25% by weight (Takamatsu Oil Co., Ltd., PES Resin S-680EA) Ethyl acetate 75% by mass

[0089] Example 4 A coating layer-forming solution having the following composition was applied to the corona-treated surface of the biaxially oriented polypropylene film and dried to form a coating layer having a thickness of 0.5 μm, thereby obtaining a multilayer substrate of the present invention. (Composition of coating solution for forming coating layer) Polyethyleneimine 60% by mass (Epomin P-1000, manufactured by Nippon Shokubai Co., Ltd.) Methanol 40% by weight

[0090] Example 5 A solution for forming a coating layer prepared as described below was applied to the corona-treated surface of the biaxially oriented polypropylene film and dried to form a coating layer having a thickness of 0.5 μm, thereby obtaining a multilayer substrate of the present invention.

[0091] A hydroxyl-containing (meth)acrylic resin (number average molecular weight 25,000, glass transition temperature 99°C, hydroxyl value 80 mg KOHL / g) was diluted with a mixed solvent of methyl ketone and ethyl acetate (mixing ratio 1:1) to a solid concentration of 10 mass% to prepare the base resin. A solution containing tolylene diisocyanate in ethyl acetate (solid content 75% by mass) was added to the base material as a curing agent to obtain a coating layer forming solution. The amount of the curing agent used was 10 parts by mass per 100 parts by mass of the base material.

[0092] Example 6 An aqueous polyamide emulsion solution was applied to the corona-treated surface of the biaxially oriented polypropylene film and dried to form a coating layer having a thickness of 0.5 μm, thereby obtaining a multilayer substrate of the present invention.

[0093] Comparative Example 1 A biaxially oriented polypropylene film (ME-1, manufactured by Mitsui Chemicals Tocello Inc.) having a thickness of 20 μm and one surface of which was corona-treated was prepared.

[0094] <<Gas barrier property evaluation>> A silica vapor deposition film was formed by CVD on the coating layer of the multi-layer base obtained in the above Example and on the corona-treated surface of the polypropylene film obtained in the above Comparative Example. After forming the deposited film, the oxygen permeability (cc / m 2 ·day·atm) and water vapor transmission rate (g / m 2 ·day) was measured by the following method, and the results are summarized in Table 1.

[0095] [Oxygen permeability] Using an oxygen permeability measuring device (OX-TRAN2 / 20 manufactured by MOCON), the test piece was set so that the substrate layer surface was the oxygen supply side, and the oxygen permeability was measured in an environment of 23°C and a relative humidity of 90% RH in accordance with JIS K 7126. [Water vapor permeability] Using a water vapor permeability measuring device (MOCON, PERMATRAN-w 3 / 33), the test piece was set so that the substrate layer surface was the water vapor supply side, and the water vapor permeability was measured in an environment of 40°C and relative humidity 90% RH in accordance with JIS K 7129.

[0096] In addition, silica and alumina deposition films were formed by the PVD method, and the oxygen permeability (cc / m 2 ·day·atm) and water vapor transmission rate (g / m 2 ·day) were measured and the results are summarized in Table 1.

[0097] <<Laminate strength test>> In the gas barrier property evaluation, a laminate was prepared by dry laminating a 40 μm-thick unstretched polypropylene film on a silica vapor deposition film formed on a substrate by a CVD method. The laminate was cut into a 15 mm wide strip and the laminate strength (N / 15 mm) between the vapor-deposited film and the coating layer, and between the vapor-deposited film and the polypropylene film was measured using a tensile tester (Tensilon universal material testing machine, manufactured by Orientec Co., Ltd.) in accordance with JIS K6854-2, at a peel speed of 50 mm / min and 90° peeling (T-peel method). The measurement results are summarized in Table 1. A 40 μm-thick unstretched polypropylene film was dry laminated onto the silica vapor deposition film and alumina vapor deposition film formed by the PVD method to prepare a laminate, and the laminate strength was measured in the same manner as above. The measurement results are summarized in Table 1.

[0098] [Table 1] [Explanation of symbols]

[0099] 10: multi-layer base material, 11: polypropylene resin layer, 12: coating layer, 20: laminated film, 21: vapor deposition film, 22: barrier coating layer, 30: laminate, 31: sealant layer, 40: packaging material, 41: body (side sheet), 42: bottom (bottom sheet), 43: gusset

Claims

1. A multi-layer substrate, The multilayer substrate includes at least a polypropylene resin layer and a coating layer, The polypropylene resin layer is subjected to a stretching treatment, and wherein the coating layer contains a resin material having a polar group.

2. The multilayer substrate according to claim 1 , wherein a ratio of a thickness of the coating layer to a total thickness of the multilayer substrate is 1% or more and 20% or less.

3. 3. The multilayer substrate according to claim 1, wherein the coating layer has a thickness of 0.1 μm or more and 10 μm or less.

4. The multilayer substrate according to any one of claims 1 to 3, wherein the resin material is one or more resin materials selected from ethylene vinyl alcohol copolymer (EVOH), polyvinyl alcohol (PVA), polyester, polyethyleneimine, hydroxyl group-containing (meth)acrylic resin, nylon 6, nylon 6,6, MXD nylon, amorphous nylon, and polyurethane.

5. The multilayer substrate according to any one of claims 1 to 4, wherein the coating layer is a layer formed using a water-based emulsion or a solvent-based emulsion.

6. The multi-layer substrate according to any one of claims 1 to 5, which is used for packaging material applications.

7. 7. A laminated film comprising the multilayer substrate according to claim 1 and a vapor-deposited film containing an inorganic oxide, the vapor-deposited film being provided on the coating layer.

8. The laminated film according to claim 7 , wherein the inorganic oxide comprises silica or alumina.

9. The laminate film according to claim 7 or 8, further comprising a barrier coat layer on the vapor-deposited film.

10. A laminate comprising the laminate film according to any one of claims 7 to 9 and a sealant layer.

11. The sealant layer is made of the same material as the polypropylene resin layer, The laminate of claim 10, wherein the homogenous material is polypropylene.

12. A packaging material comprising a laminate according to claim 10 or 11.

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