JP2023168377A - Laminate for packaging material and packaging material - Google Patents

Abstract

To provide a laminate for a packaging material capable of obtaining a packaging material having excellent recyclability while having strength or barrier properties as a packaging material.SOLUTION: There is provided a laminate for a packaging material which comprises at least a substrate, an adhesion layer and a heat seal layer, wherein the substrate comprises a substrate body and a first vapor deposition film, the heat seal layer comprises a second vapor deposition film and a polyolefin resin layer, the substrate body is a stretched resin film composed of a polyolefin, a polyolefin constituting the substrate body and a polyolefin constituting the polyolefin resin layer of the heat seal layer is the same polyolefin, the thickness of the first vapor deposition film is smaller than that of the substrate body and the thickness of the second vapor deposition film is smaller than that of the polyolefin resin layer.SELECTED DRAWING: Figure 1

Description

The present invention relates to a laminate for packaging material and a packaging material composed of the laminate.

Conventionally, a resin film made of a resin material has been used as a constituent material of a packaging material. For example, resin films made of polyolefins have appropriate flexibility and transparency, and have excellent heat sealability, and are therefore widely used as packaging materials.

Normally, resin films made of polyolefin cannot be used as base materials due to their inferior strength and heat resistance, and are used by laminating them with resin films made of polyester, polyamide, etc. A typical packaging material is composed of a laminated film in which the base material and the heat-sealing layer are made of different resin materials (for example, Patent Document 1).

In recent years, with increasing calls for building a recycling-oriented society, packaging materials with high recyclability are being sought. However, as described above, conventional packaging materials are composed of different types of resin materials, and it is difficult to separate each resin material, so it is currently not recycled.

Japanese Patent Application Publication No. 2009-202519

The present inventors have discovered that polyolefin resin, which has conventionally been used as a heat seal layer, can be used as a base material by making it into a stretched resin film, and that the base material can be used as a heat seal layer with a polyolefin resin layer made of the same polyolefin. It has been found that by using it in combination with a sealing layer, it is possible to create a packaging material that has sufficient strength and heat resistance as a packaging material and is recyclable.
In addition, the present inventors have found that by configuring the base material and the heat seal layer to each have a vapor-deposited film, it is possible to obtain a packaging material that has high barrier performance while maintaining recyclability. Ta.

The present invention has been made in view of the above knowledge, and an object of the present invention is to provide a packaging material that has strength and barrier properties as a packaging material and also has excellent recyclability. An object of the present invention is to provide a laminate.
Moreover, the problem to be solved by the present invention is to provide a packaging material composed of the laminate for packaging material.

The laminate for packaging materials of the present invention includes at least a base material, an adhesive layer, and a heat seal layer,
The base material includes a base material body and a first vapor deposited film,
The heat sealing layer includes a second vapor deposited film and a polyolefin resin layer,
The base material body is a stretched resin film made of polyolefin,
The polyolefin constituting the base material body and the polyolefin constituting the polyolefin resin layer of the heat seal layer are the same polyolefin,
The thickness of the first vapor deposited film is smaller than the thickness of the base material main body,
The second vapor deposited film is characterized in that the thickness is smaller than the thickness of the polyolefin resin layer.

In one embodiment of the invention, the substrate further includes a barrier coat layer on the first deposited film.

In one embodiment of the present invention, the second vapor-deposited film is an aluminum vapor-deposited film, and the adhesive layer includes a cured product of a resin composition containing a polyester polyol, an isocyanate compound, and a phosphoric acid-modified compound.

In one embodiment of the present invention, the content of polyolefin in the entire laminate for packaging material is 80% by mass or more.

The packaging material of the present invention is characterized by being composed of the above-mentioned laminate.

According to the present invention, a packaging material laminate having high recyclability can be provided.

Further, according to the present invention, it is possible to provide a laminate for packaging material having high strength, heat resistance, oxygen barrier properties, and water vapor barrier properties.

Furthermore, according to the present invention, it is possible to provide a packaging material composed of the laminate for packaging material.

BRIEF DESCRIPTION OF THE DRAWINGS It is a cross-sectional schematic diagram which shows one Embodiment of the laminated body for packaging materials of this invention. BRIEF DESCRIPTION OF THE DRAWINGS It is a cross-sectional schematic diagram which shows one Embodiment of the laminated body for packaging materials of this invention. BRIEF DESCRIPTION OF THE DRAWINGS It is a cross-sectional schematic diagram which shows one Embodiment of the laminated body for packaging materials of this invention. BRIEF DESCRIPTION OF THE DRAWINGS It is a perspective view showing one Embodiment of the packaging material produced using the laminated body for packaging materials of this invention. BRIEF DESCRIPTION OF THE DRAWINGS It is a perspective view showing one Embodiment of the packaging material produced using the laminated body for packaging materials of this invention.

(Laminated body for packaging materials)
As shown in FIG. 1, the laminate 10 for packaging materials of the present invention comprises a base material 13 including a base material body 11 and a first vapor deposited film 12, an adhesive layer 14, a second vapor deposited film 15, and a polyolefin resin. A heat-sealing layer 17 comprising a layer 16.

Further, in one embodiment of the present invention, the base material 13 may include a barrier coat layer 18 on the first vapor deposited film 12, as shown in FIG.

Moreover, in one embodiment of the present invention, as shown in FIG. 3, in the packaging material laminate 10, the polyolefin resin layer 16 includes a first polyolefin resin layer 19 and a second polyolefin resin layer 20. It's okay.

The content of the same polyolefin in the entire laminate for packaging materials of the present invention is preferably 80% by mass or more, more preferably 90% by mass or more.
By setting the content of the same polyolefin in the entire laminate for packaging materials of the present invention to 80% by mass or more, the recyclability of the laminate for packaging materials of the present invention can be improved.
Note that the content of the same polyolefin in the laminate for packaging material means the ratio of the content of the same polyolefin to the sum of the contents of resin materials in each layer constituting the laminate.

Each layer constituting the packaging material laminate of the present invention will be explained below.

(Base material)
The base material includes at least a base material body and a first vapor deposited film. Further, in one embodiment, the base material can include a barrier coat layer on the first deposited film.

The present invention is characterized in that the thickness of the first vapor deposited film is smaller than the thickness of the base material body. With such a configuration, the recyclability of the packaging material laminate of the present invention can be improved.
The thickness of the first vapor deposited film is preferably smaller than the thickness of the base material body by 5 μm or more, more preferably 10 μm or more smaller. When the thickness of the first vapor-deposited film is 5 μm or more smaller than the thickness of the base material body, the recyclability of the packaging material laminate of the present invention can be further improved.

(base material body)
The base material main body is made of polyolefin, and the same polyolefin as the polyolefin constituting the polyolefin resin layer described below is used as this polyolefin. By using the same polyolefin as the polyolefin constituting the base material body and the polyolefin constituting the polyolefin resin layer, the recyclability of the laminate for packaging material can be improved.

The main body of the base material is a stretched resin film made of polyolefin in order to maintain strength and heat resistance as a packaging material. The stretched resin film may be a uniaxially stretched resin film or a biaxially stretched resin film.

The stretching ratio in the longitudinal direction (MD) of the stretched resin film is preferably 2 times or more and 10 times or less, and preferably 3 times or more and 7 times or less.
By setting the stretching ratio of the stretched resin film in the longitudinal direction (MD) to 2 times or more, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Moreover, since the transparency of the base material main body can be improved, when an image is formed on the first vapor deposited film side surface of the base material main body, the visibility can be improved. On the other hand, the upper limit of the stretching ratio in the longitudinal direction (MD) of the stretched resin film is not particularly limited, but from the viewpoint of the breaking limit of the stretched resin film, it is preferably 10 times or less.

Further, the stretching ratio of the stretched resin film in the transverse direction (TD) is preferably 2 times or more and 10 times or less, and preferably 3 times or more and 7 times or less.
By setting the stretching ratio of the stretched resin film in the transverse direction (TD) to 2 times or more, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Moreover, since the transparency of the base material main body can be improved, when an image is formed on the first vapor deposited film side surface of the base material main body, the visibility can be improved. On the other hand, the upper limit of the stretching ratio in the transverse direction (TD) of the stretched resin film is not particularly limited, but from the viewpoint of the breaking limit of the stretched resin film, it is preferably 10 times or less.

The polyolefin that can be used as the base material body must be the same polyolefin as the polyolefin resin constituting the heat seal layer as described above, and examples of such polyolefins include polyethylene, polypropylene, polymethylpentene, Examples include ethylene-propylene copolymers and propylene-butene copolymers, among which polyethylene and polypropylene are preferred.

Examples of polyethylene include high-density polyethylene (HDPE) with a density of more than 0.945 g/cm ³ , medium-density polyethylene (MDPE) with a density of 0.925 to 0.945 g/cm ³ , and density less than 0.925 g/cm ³ low density polyethylene (LDPE) and linear low density polyethylene (LLDPE).

In one embodiment, the base material body includes a layer made of high-density polyethylene (hereinafter referred to as a high-density polyethylene layer) and a layer made of medium-density polyethylene (hereinafter referred to as a medium-density polyethylene layer). be able to.
By providing a high-density polyethylene layer on the outside of the base material body, the strength and heat resistance of the packaging material laminate of the present invention can be improved. Further, by providing the medium density polyethylene layer, the stretching suitability of the resin film constituting the base material main body can be improved.

For example, it has a structure consisting of a high-density polyethylene layer/medium-density polyethylene layer from the outside.
With such a configuration, the stretching suitability of the resin film can be improved.
Moreover, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved.
At this time, the thickness of the high-density polyethylene layer is preferably thinner than the thickness of the medium-density polyethylene layer.
The ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer is preferably 1/10 or more and 1/1 or less, and more preferably 1/5 or more and 1/2 or less.
By setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer to 1/10 or more, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Further, by setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer to 1/1 or less, the stretching suitability of the resin film can be improved.

Alternatively, for example, it may be configured to consist of a high-density polyethylene layer/medium-density polyethylene layer/high-density polyethylene layer from the outside.
With such a configuration, the stretching suitability of the resin film can be improved.
Moreover, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Furthermore, it is possible to prevent curling in the base material body.
At this time, the thickness of the high-density polyethylene layer is preferably thinner than the thickness of the medium-density polyethylene layer.
The ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer is preferably 1/10 or more and 1/1 or less, and more preferably 1/5 or more and 1/2 or less.
By setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer to 1/10 or more, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Further, by setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer to 1/1 or less, the stretching suitability of the resin film can be improved.

Alternatively, for example, the structure may be made of a high density polyethylene layer/medium density polyethylene layer/low density polyethylene layer or a linear low density polyethylene layer/medium density polyethylene layer/high density polyethylene layer from the outside.
With such a configuration, the stretching suitability of the resin film can be improved.
Moreover, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Further, it is possible to prevent curling in the base material body. Furthermore, the processability of the resin film can be improved.
At this time, the thickness of the high-density polyethylene layer is preferably thinner than the thickness of the medium-density polyethylene layer.
The ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer is preferably 1/10 or more and 1/1 or less, and more preferably 1/5 or more and 1/2 or less.
By setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer to 1/10 or more, the strength and heat resistance of the laminate for packaging materials of the present invention can be improved. Further, by setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the medium-density polyethylene layer to 1/1 or less, the stretching suitability of the resin film can be improved.
Further, the thickness of the high-density polyethylene layer is preferably thinner than the thickness of the low-density polyethylene layer or the linear low-density polyethylene layer.
The ratio of the thickness of the high-density polyethylene layer to the thickness of the low-density polyethylene layer or the linear low-density polyethylene layer is preferably 1/10 or more and 1/1 or less, and 1/5 or more and 1/2 or less. It is more preferable that there be.
Heat resistance can be improved by setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the low-density polyethylene layer or the linear low-density polyethylene layer to 1/10 or more.
Further, by setting the ratio of the thickness of the high-density polyethylene layer to the thickness of the low-density polyethylene layer or the linear low-density polyethylene layer to 1/1 or less, the processability of stretching can be improved.

Polypropylene may be a homopolymer, a random copolymer or a block copolymer.
A polypropylene homopolymer is a polymer of only propylene, and a polypropylene random copolymer is a polymer of propylene and other α-olefins other than propylene (for example, ethylene, butene-1, 4-methyl-1-pentene, etc.). It is a random copolymer, and the polypropylene block copolymer is a copolymer having a polymer block made of propylene and a polymer block made of other α-olefins other than the above-mentioned propylene.
Among these polypropylenes, from the viewpoint of being able to improve the transparency of the base material body and improving the visibility when an image is formed on the first vapor deposited film side surface of the base material body, Preference is given to using homopolymers or random copolymers. When the rigidity and heat resistance of the packaging material are important, a homopolymer can be used, and when the impact resistance and the like are important, a random copolymer can be used.

Moreover, as a raw material for obtaining polyolefin, an olefin monomer derived from biomass may be used instead of an olefin monomer obtained from fossil fuel. Since such biomass-derived olefin monomers are carbon-neutral materials, they can be used as packaging materials with even less environmental impact.
Such biomass-derived polyolefin, for example, polyethylene, can be produced by a method as described in JP-A-2013-177531. Furthermore, commercially available biomass-derived polyolefins (for example, green PE commercially available from Braskem, etc.) may be used.

Moreover, polyolefin recycled by mechanical recycling can also be used. Mechanical recycling generally refers to the process of crushing recovered polyolefin films, washing them with alkali to remove dirt and foreign matter from the film surface, and then drying them at high temperature and reduced pressure for a certain period of time to remain inside the film. This method performs decontamination by diffusing contaminants, removes dirt from polyolefin film, and returns it to polyolefin.

The base material main body may have an image formed on its surface. The image may be formed on any surface of the base material body, but it is preferable to form the image on the first vapor deposited film side surface because it can prevent contact with the outside air and prevent deterioration over time. is preferred.
Furthermore, the image formed is not particularly limited, and may include characters, patterns, symbols, and combinations thereof.
Although the image can be formed using a conventionally known ink, it is preferably performed using an ink derived from biomass. As a result, packaging materials with less environmental load can be produced using the laminate of the present invention.
The image forming method is not particularly limited, and conventionally known printing methods such as gravure printing, offset printing, and flexographic printing can be used. Among these, flexographic printing is preferred because it can reduce environmental impact.

Moreover, it is preferable that the base material main body is subjected to a surface treatment. Thereby, adhesion between adjacent layers can be improved.
The surface treatment method is not particularly limited, and includes physical treatments such as corona discharge treatment, ozone treatment, low-temperature plasma treatment using oxygen gas and/or nitrogen gas, glow discharge treatment, and oxidation using chemicals. Examples include chemical treatments such as treatment.
Alternatively, an anchor coat layer may be formed on the surface of the base material using a conventionally known anchor coat agent.

The thickness of the base material body is preferably 5 μm or more and 300 μm or less, more preferably 7 μm or more and 100 μm or less.
By setting the thickness of the base material body to 5 μm or more, the strength of the packaging material laminate of the present invention can be improved. Further, by setting the thickness of the base material body to 300 μm or less, the processability of the laminate for packaging materials of the present invention can be improved.

The base material main body can be produced by forming a polyolefin film by a T-die method or an inflation method, producing a film, and then stretching the film.
According to the inflation method, film formation and stretching can be performed simultaneously.

When producing the base material body by the T-die method, the MFR of the polyolefin is preferably 5 g/10 minutes or more and 20 g/10 minutes or less.
By setting the MFR of the polyolefin to 5 g/10 minutes or more, the processability of the laminate for packaging materials of the present invention can be improved. Further, by setting the MFR of the polyolefin to 20 g/10 minutes or less, it is possible to prevent the resin film from breaking.

When producing the base material body by the inflation method, the MFR of the polyolefin is preferably 0.5 g/10 minutes or more and 5 g/10 minutes or less.
By setting the MFR of the polyolefin to 0.5 g/10 minutes or more, the processability of the laminate for packaging materials of the present invention can be improved. Further, by controlling the MFR of the polyolefin to 5 g/10 minutes or less, film formability can be improved.

Note that the base material main body is not limited to one produced by the above method, and a commercially available one may be used.

(First vapor deposited film)
The base material of the present invention includes a first vapor deposited film on the base material body. Thereby, the oxygen barrier properties and water vapor barrier properties of the laminate for packaging materials of the present invention can be improved.

The first vapor deposited film is composed of a metal such as aluminum, and an inorganic oxide such as aluminum oxide, silicon oxide, magnesium oxide, calcium oxide, zirconium oxide, titanium oxide, boron oxide, hafnium oxide, barium oxide, etc. A vapor deposited film can be mentioned.
When forming an image on the surface of the barrier coat layer described below, the first vapor deposited film is required to have transparency, and in this case, the first vapor deposited film is preferably an inorganic oxide vapor deposited film.

Further, the thickness of the first vapor deposited 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 setting the thickness of the first vapor-deposited film to 1 nm or more, the oxygen barrier properties and water vapor barrier properties of the packaging material laminate of the present invention can be further improved. Further, by setting the thickness of the first vapor deposited film to 150 nm or less, it is possible to prevent the occurrence of cracks in the first vapor deposited film, and to improve the recyclability of the laminate for packaging materials of the present invention. I can do it.

For the first vapor deposited film to be an aluminum vapor deposited film, the OD value thereof is preferably 2 or more and 3.5 or less. Thereby, it is possible to improve the oxygen barrier properties and water vapor barrier properties while maintaining the productivity of the laminate for packaging materials of the present invention. In the present invention, the OD value can be measured in accordance with JIS-K-7361.

The first vapor deposition film can be formed using a conventionally known method, for example, a physical vapor deposition method (PVD method) such as a vacuum evaporation method, a sputtering method, and an ion plating method; Further examples include chemical vapor deposition (CVD) methods such as plasma chemical vapor deposition, thermal chemical vapor deposition, and photochemical vapor deposition.

Furthermore, for example, a composite film consisting of two or more layers of vapor-deposited films of different types of inorganic oxides can be formed and used by using both physical vapor deposition and chemical vapor deposition. The degree of vacuum in the deposition chamber is preferably about 10 ^-2 to 10 ^-8 mbar before introducing oxygen, and preferably about 10 ^-1 to 10 ^-6 mbar after introducing oxygen. Note that the amount of oxygen introduced varies depending on the size of the vapor 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 within a range that does not cause any problem. The transport speed of the film can be approximately 10 to 800 m/min.

The surface of the first vapor deposited film is preferably subjected to the above surface treatment. Thereby, adhesion between adjacent layers can be improved.

(barrier coat layer)
The base material of the present invention can be provided with a barrier coat layer on the first vapor deposited film. Thereby, the oxygen barrier properties and water vapor barrier properties of the laminate for packaging materials of the present invention can be further improved.

In one embodiment, the barrier coat layer comprises polyamides, polyesters, such as ethylene-vinyl alcohol copolymer (EVOH), polyvinyl alcohol, polyacrylonitrile, nylon 6, nylon 6,6, and polymethaxylylene adipamide (MXD6), Contains gas barrier resins such as polyurethane and (meth)acrylic resins.

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, more preferably 75% by mass or more and 90% by mass or less. By setting the content of the gas barrier resin in the barrier coat layer to 50% by mass or more, the oxygen barrier properties and water vapor barrier properties of the laminate for packaging materials of the present invention can be further improved.

The barrier coat layer can contain additives within a range that does not impair the characteristics of the present invention. Examples of additives include crosslinking agents, antioxidants, antiblocking agents, slip agents, ultraviolet absorbers, light stabilizers, fillers, reinforcing agents, antistatic agents, compatibilizers, and pigments. It will be done.

The thickness of the barrier coat layer is preferably 0.01 μm or more and 10 μm or less, more preferably 0.1 μm or more and 5 μm or less. By setting the thickness of the barrier coat layer to 0.01 μm or more, the oxygen barrier properties and water vapor barrier properties of the packaging material laminate of the present invention can be further improved. Moreover, when it is provided adjacent to an inorganic oxide vapor deposited film, it is possible to prevent cracks from occurring in the vapor deposited film.
By setting the thickness of the barrier coat layer to 10 μm or less, the recyclability of the packaging material laminate of the present invention can be improved.

The barrier coat layer can be formed by dissolving or dispersing the above material in water or a suitable solvent, applying the solution onto the first vapor deposited film, and drying the solution. The barrier coat layer can also be formed by applying a commercially available barrier coat agent onto the deposited film and drying it.

In another embodiment, the barrier coat layer is 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 method catalyst, water, an organic solvent, etc. It is a gas barrier coating film containing at least one resin composition such as a hydrolyzate of or a hydrolyzed condensate of a metal alkoxide.
When the first vapor deposited film provided on the base material is an inorganic oxide vapor deposited film, by using the gas barrier coating film as the barrier coat layer, it is possible to effectively prevent the occurrence of cracks in the vapor deposited film.

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

As the metal atom M, silicon, zirconium, titanium, aluminum, etc. can be used, for example.
Furthermore, examples of the organic group represented by R ¹ and R ² include alkyl groups such as methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, and i-butyl group. I can do it.

Examples of metal alkoxides satisfying the above general formula include tetramethoxysilane (Si(OCH ₃ ) ₄ ), tetraethoxysilane (mass%) Si(OC ₂ H ₅ ) ₄ ), and tetrapropoxysilane (Si(OC ₃ H ₇ ) ₄ ), tetrabutoxysilane (Si(OC ₄ H ₉ ) ₄ ), and the like.

Moreover, it is preferable that a silane coupling agent is used together with the metal alkoxide.
As the silane coupling agent, known organoalkoxysilanes containing organic reactive groups can be used, but organoalkoxysilanes containing epoxy groups are particularly preferred. Examples of the organoalkoxysilane having an epoxy group include γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, and β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane. It will be done.

Two or more types of silane coupling agents as described above may be used, and the silane coupling agents are used in an amount of about 1 to 20 parts by mass based on 100 parts by mass of the total amount of the alkoxides. It is preferable.

As the water-soluble polymer, polyvinyl alcohol and 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 preferable to use these in combination.

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 based on 100 parts by mass of the metal alkoxide.
By setting the content of water-soluble polymer in the gas barrier coating film to 5 parts by mass or more per 100 parts by mass of metal alkoxide, the oxygen barrier properties and water vapor barrier properties of the laminate for packaging materials of the present invention are further improved. can do. Further, by controlling the content of the water-soluble polymer in the gas barrier coating film to 500 parts by mass or less based on 100 parts by mass of the metal alkoxide, the film formability of the gas barrier coating film can be improved.

The thickness of the gas barrier coating film is preferably 0.01 μm or more and 100 μm or less, more preferably 0.1 μm or more and 50 μm or less. This makes it possible to further improve oxygen barrier properties and water vapor barrier properties while maintaining recyclability.
By setting the thickness of the gas barrier coating film to 0.01 μm or more, the oxygen barrier properties and water vapor barrier properties of the packaging material laminate of the present invention can be improved. Moreover, when it is provided adjacent to an inorganic oxide vapor deposited film, it is possible to prevent cracks from occurring in the vapor deposited film.

The gas barrier coating film is prepared by applying the composition containing the above-mentioned materials to the first vapor deposited film by conventionally known means such as roll coating using a gravure roll coater, spray coating, spin coating, dipping, brush, barcode, applicator, etc. It can be formed by coating the composition on top and polycondensing the composition by a sol-gel method.
As the sol-gel method catalyst, acid or amine compounds are suitable. As the amine compound, tertiary amines that are substantially insoluble in water and soluble in organic solvents are suitable, such as N,N-dimethylbenzylamine, tripropylamine, tributylamine, tripentyl Examples include amines. Among these, N,N-dimethylbenzylamine is preferred.
The sol-gel method catalyst is preferably used in a range of 0.01 parts by mass or more and 1.0 parts by mass or less, and 0.03 parts by mass or more and 0.3 parts by mass or less, per 100 parts by mass of metal alkoxide. It is more preferable.
By setting the amount of the sol-gel method catalyst to be 0.01 parts by mass or more per 100 parts by mass of metal alkoxide, the catalytic effect can be improved. Further, by controlling the amount of the sol-gel method catalyst to be 1.0 parts 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.

The composition may further contain an acid. Acids are used as catalysts in the sol-gel process, mainly for the hydrolysis of alkoxides, silane coupling agents, and the like.
As the acid, mineral acids such as sulfuric acid, hydrochloric acid, and nitric acid, and organic acids such as acetic acid and tartaric acid are used. The amount of 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 (for example, silicate portion) of the silane coupling agent.
The catalytic effect can be improved by setting the amount of the acid used to be 0.001 mol or more based on the total molar amount of the alkoxide and the alkoxide portion (eg, silicate portion) of the silane coupling agent. In addition, by setting the total molar amount of the alkoxide and the alkoxide component (for example, silicate portion) of the silane coupling agent to 0.05 mole or less, the thickness of the gas barrier coating film formed can be made uniform. can.

Further, the above composition may contain water in a proportion of preferably 0.1 mol or more and 100 mols or less, more preferably 0.8 mol or more and 2 mols or less, per 1 mol of the total molar amount of the alkoxide. preferable.
By setting the water content to 0.1 mol or more per 1 mol of the total molar amount of alkoxide, the oxygen barrier properties and water vapor barrier properties of the laminate for packaging materials of the present invention can be improved. Furthermore, by setting the water content to 100 mol or more per 1 mol of the total molar amount of alkoxide, the hydrolysis reaction can be carried out quickly.

Further, the above composition may contain an organic solvent. As the organic solvent, for example, methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butanol, etc. can be used.

An embodiment of a method for forming a gas barrier coating film will be described below.
First, a metal alkoxide, a water-soluble polymer, a sol-gel catalyst, water, an organic solvent, and if necessary a silane coupling agent are mixed to prepare a composition. A polycondensation reaction gradually proceeds in the composition.
Next, the composition is applied onto the deposited film by the conventionally known method described above and dried.
By this drying, the polycondensation reaction of the alkoxide and the water-soluble polymer (and the silane coupling agent if the composition includes the silane coupling agent) further proceeds, and a composite polymer layer is formed.
Finally, a gas barrier coating film can be formed by heating the composition at a temperature of 20 to 250°C, preferably 50 to 220°C, for 1 second to 10 minutes.

The barrier coat layer may have an image formed on its surface. The image forming method and the like are as described above.

(Adhesive layer)
The laminate for packaging material of the present invention includes an adhesive layer between the base material and the heat seal layer.

The adhesive layer includes at least one type of adhesive, and may be a one-component curing type, a two-component curing type, or a non-curing type adhesive. Further, the adhesive may be a solvent-free adhesive or a solvent-based adhesive, but from the viewpoint of environmental load, a solvent-free adhesive can be preferably used.
Examples of solvent-free adhesives include polyether adhesives, polyester adhesives, silicone adhesives, epoxy adhesives, and urethane adhesives. Among these, two-component curable urethane adhesives adhesives can be preferably used.
Examples of solvent-based adhesives include rubber adhesives, vinyl adhesives, silicone adhesives, epoxy adhesives, phenolic adhesives, and olefin adhesives.

In addition, in the packaging material laminate of the present invention, when at least one of the first vapor deposited film and the second vapor deposited film is an aluminum vapor deposited film, the adhesive layer is made of a polyester polyol, an isocyanate compound, and a phosphoric acid modified It is preferable to use a cured product of a resin composition containing the compound.
By configuring the adhesive layer in this manner, the oxygen barrier properties and water vapor barrier properties of the packaging material laminate of the present invention can be further improved.
When a laminate including a vapor-deposited film is applied to a packaging material, a bending load is applied to the laminate by a molding machine or the like, which may cause cracks or the like to occur in the aluminum vapor-deposited film. By using the specific adhesive as described above, even if cracks occur in the aluminum vapor-deposited film, deterioration in oxygen barrier properties and water vapor barrier properties can be suppressed.

Polyester polyol has two or more hydroxyl groups in one molecule as a functional group. Further, the isocyanate compound has two or more isocyanate groups in one molecule as a functional group.
A polyester polyol has, for example, a polyester structure or a polyester polyurethane structure as a main skeleton.

As a specific example of the resin composition containing a polyester polyol, an isocyanate compound, and a phosphoric acid modified compound, the PASLIM series sold by DIC Corporation can be used.

The resin composition may further contain a plate-like inorganic compound, a coupling agent, a cyclodextrin and/or a derivative thereof, and the like.

As the polyester polyol having two or more hydroxyl groups in one molecule as a functional group, the following [Example 1] to [Example 3] can be used, for example.
[First example] Polyester polyol obtained by polycondensation of ortho-oriented polycarboxylic acid or its anhydride and polyhydric alcohol [Second example] Polyester polyol having a glycerol skeleton [Third example] Having an isocyanuric ring Polyester Polyol Each polyester polyol will be explained below.

The polyester polyol according to the first example is selected from the group consisting of a polyhydric carboxylic acid component containing at least one orthophthalic acid and its anhydride, and ethylene glycol, propylene glycol, butylene glycol, neopentyl glycol, and cyclohexanedimethanol. It is a polycondensate obtained by polycondensation with a polyhydric alcohol component containing at least one type of alcohol.
Particularly preferred is a polyester polyol in which the content of orthophthalic acid and its anhydride is 70 to 100% by mass based on the total polyhydric carboxylic acid components.

The polyester polyol according to the first example essentially contains orthophthalic acid and its anhydride as a polycarboxylic acid component, but other polycarboxylic acid components may be copolymerized to the extent that the effects of this embodiment are not impaired. It's okay.
Specifically, aliphatic polycarboxylic acids such as succinic acid, adipic acid, azelaic acid, sebacic acid and dodecanedicarboxylic acid, unsaturated bond-containing polycarboxylic acids such as maleic anhydride, maleic acid and fumaric acid, 1, Alicyclic polycarboxylic acids such as 3-cyclopentanedicarboxylic acid and 1,4-cyclohexanedicarboxylic acid, terephthalic acid, isophthalic acid, pyromellitic acid, trimellitic acid, 1,4-naphthalenedicarboxylic acid, 2,5- Naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, naphthalic acid, biphenyldicarboxylic acid, 1,2-bis(phenoxy)ethane-p,p'-dicarboxylic acid, anhydrides of these dicarboxylic acids, and ester formation of these dicarboxylic acids Examples include aromatic polycarboxylic acids such as dihydroxy derivatives, polybasic acids such as p-hydroxybenzoic acid, p-(2-hydroxyethoxy)benzoic acid, and ester-forming derivatives of these dihydroxycarboxylic acids. Among these, succinic acid, 1,3-cyclopentanedicarboxylic acid, and isophthalic acid are preferred.
Note that two or more types of the other polyhydric carboxylic acids mentioned above may be used.

As the polyester polyol according to the second example, a polyester polyol having a glycerol skeleton represented by the general formula (1) can be mentioned.
In the general formula (1), R ₁ , R ₂ , and R ₃ are each independently H (hydrogen atom) or a group represented by the following general formula (2).

In formula (2), n represents an integer of 1 to 5, and X is a 1,2-phenylene group, a 1,2-naphthylene group, a 2,3-naphthylene group, 2, represents an arylene group selected from the group consisting of a 3-anthraquinonediyl group and a 2,3-anthracenediyl group, and Y represents an alkylene group having 2 to 6 carbon atoms.
However, at least one of R ₁ , R ₂ , and R ₃ represents a group represented by general formula (2).

In general formula (1), at least one of R ₁ , R ₂ , and R ₃ needs to be a group represented by general formula (2). Among these, it is preferable that all of R ₁ , R ₂ , and R ₃ are groups represented by general formula (2).

Further, a compound in which any one of R ₁ , R ₂ , and R ₃ is a group represented by general formula (2), and a compound in which any two of R ₁ , R ₂ , and R ₃ are represented by general formula (2) A mixture of two or more of a compound in which R ₁ , R ₂ , and R ₃ are all groups represented by general formula (2) may be used.

X is selected from the group consisting of 1,2-phenylene group, 1,2-naphthylene group, 2,3-naphthylene group, 2,3-anthraquinonediyl group and 2,3-anthracenediyl group, and has a substituent. represents an optionally substituted arylene group.
When X is substituted with a substituent, it may be substituted with one or more substituents, and the substituent is bonded to any carbon atom on X that is different from the radical. Examples of the substituent include a chloro group, a bromo group, a methyl group, an ethyl group, an i-propyl group, a hydroxyl group, a methoxy group, an ethoxy group, a phenoxy group, a methylthio group, a phenylthio group, a cyano group, a nitro group, an amino group, Examples include phthalimide group, carboxyl group, carbamoyl group, N-ethylcarbamoyl group, phenyl group, and naphthyl group.

In general formula (2), Y is an ethylene group, a propylene group, a butylene group, a neopentylene group, a 1,5-pentylene group, a 3-methyl-1,5-pentylene group, a 1,6-hexylene group, a methylpentylene group. and alkylene groups having 2 to 6 carbon atoms, such as dimethylbutylene groups. Among them, Y is preferably a propylene group or an ethylene group, and most preferably an ethylene group.

The polyester resin compound having a glycerol skeleton represented by the general formula (1) contains glycerol, an aromatic polycarboxylic acid or anhydride thereof in which a carboxylic acid is substituted at the ortho position, and a polyhydric alcohol component as essential components. It can be synthesized by reacting as

Examples of the aromatic polycarboxylic acid or its anhydride in which carboxylic acid is substituted at the ortho position include orthophthalic acid or its anhydride, naphthalene 2,3-dicarboxylic acid or its anhydride, and naphthalene 1,2-dicarboxylic acid or its anhydride. Examples include anhydride, anthraquinone 2,3-dicarboxylic acid or its anhydride, and 2,3-anthracenecarboxylic acid or its anhydride.
These compounds may have a substituent on any carbon atom of the aromatic ring. Examples of the substituent include a chloro group, a bromo group, a methyl group, an ethyl group, an i-propyl group, a hydroxyl group, a methoxy group, an ethoxy group, a phenoxy group, a methylthio group, a phenylthio group, a cyano group, a nitro group, an amino group, Examples include phthalimide group, carboxyl group, carbamoyl group, N-ethylcarbamoyl group, phenyl group, and naphthyl group.

Further, examples of the polyhydric alcohol component include alkylene diols having 2 to 6 carbon atoms. For example, diols such as ethylene glycol, propylene glycol, butylene glycol, neopentyl glycol, 1,5-pentanediol, 3-methyl-1,5-pentanediol, 1,6-hexanediol, methylpentanediol and dimethylbutanediol can be exemplified.

The polyester polyol according to the third example is a polyester polyol having an isocyanuric ring represented by the following general formula (3).
In the general formula (3), R ₁ , R ₂ , and R ₃ each independently represent "-(CH ₂ ) n1-OH (where n1 represents an integer of 2 to 4)" or the general formula (4 ) represents the structure of

In the general formula (4), n2 represents an integer of 2 to 4, n3 represents an integer of 1 to 5, and X is a 1,2-phenylene group, a 1,2-naphthylene group, a 2,3-naphthylene group, An arylene group selected from the group consisting of a 2,3-anthraquinonediyl group and a 2,3-anthracenediyl group, which may have a substituent, and Y represents an alkylene group having 2 to 6 carbon atoms) represents a group represented by However, at least one of R ₁ , R ₂ , and R ₃ is a group represented by general formula (4).

In general formula (3), the alkylene group represented by -(CH ₂ )n1- may be linear or branched. Among them, n1 is preferably 2 or 3, and most preferably 2.

In the general formula (4), n2 represents an integer of 2 to 4, and n3 represents an integer of 1 to 5.
X is selected from the group consisting of 1,2-phenylene group, 1,2-naphthylene group, 2,3-naphthylene group, 2,3-anthraquinonediyl group, and 2,3-anthracenediyl group, and has a substituent. represents an optionally substituted arylene group.

When X is substituted with a substituent, it may be substituted with one or more substituents, and the substituent is bonded to any carbon atom on X that is different from the radical. Examples of the substituent include a chloro group, a bromo group, a methyl group, an ethyl group, an i-propyl group, a hydroxyl group, a methoxy group, an ethoxy group, a phenoxy group, a methylthio group, a phenylthio group, a cyano group, a nitro group, an amino group, Examples include phthalimide group, carboxyl group, carbamoyl group, N-ethylcarbamoyl group, phenyl group, and naphthyl group.
Among the substituents of Most preferred is phenyl.

In general formula (4), Y is an ethylene group, a propylene group, a butylene group, a neopentylene group, a 1,5-pentylene group, a 3-methyl-1,5-pentylene group, a 1,6-hexylene group, a methylpentylene group. and alkylene groups having 2 to 6 carbon atoms, such as dimethylbutylene groups. Among them, Y is preferably a propylene group or an ethylene group, and most preferably an ethylene group.

In general formula (3), at least one of R ₁ , R ₂ , and R ₃ is a group represented by general formula (4). Among these, it is preferable that all of R ₁ , R ₂ , and R ₃ are groups represented by general formula (4).

Further, a compound in which any one of R ₁ , R ₂ , and R ₃ is a group represented by general formula (4), and a compound in which any two of R ₁ , R ₂ , and R ₃ are represented by general formula (4) A mixture of two or more of a compound in which R ₁ , R ₂ , and R ₃ are all groups represented by general formula (4) may be used.

A polyester polyol having an isocyanuric ring represented by the general formula (3) is composed of a triol having an isocyanuric ring, an aromatic polycarboxylic acid in which a carboxylic acid is substituted at the ortho position or its anhydride, and a polyhydric alcohol component. Can be synthesized by reacting with as an essential component

Examples of triols having an isocyanuric ring include alkylene oxide adducts of isocyanuric acid such as 1,3,5-tris(2-hydroxyethyl)isocyanuric acid and 1,3,5-tris(2-hydroxypropyl)isocyanuric acid. Examples include.

In addition, examples of the aromatic polycarboxylic acid or its anhydride in which carboxylic acid is substituted at the ortho position include orthophthalic acid or its anhydride, naphthalene 2,3-dicarboxylic acid or its anhydride, and naphthalene 1,2-dicarboxylic acid. or its anhydride, anthraquinone 2,3-dicarboxylic acid or its anhydride, and 2,3-anthracenecarboxylic acid or its anhydride. These compounds may have a substituent on any carbon atom of the aromatic ring.

Examples of the substituent include a chloro group, a bromo group, a methyl group, an ethyl group, an i-propyl group, a hydroxyl group, a methoxy group, an ethoxy group, a phenoxy group, a methylthio group, a phenylthio group, a cyano group, a nitro group, an amino group, Examples include phthalimide group, carboxyl group, carbamoyl group, N-ethylcarbamoyl group, phenyl group, and naphthyl group.

Further, examples of the polyhydric alcohol component include alkylene diols having 2 to 6 carbon atoms. For example, diols such as ethylene glycol, propylene glycol, butylene glycol, neopentyl glycol, 1,5-pentanediol, 3-methyl-1,5-pentanediol, 1,6-hexanediol, methylpentanediol and dimethylbutanediol can be mentioned.
Among these, 1,3,5-tris(2-hydroxyethyl)isocyanuric acid or 1,3,5-tris(2-hydroxypropyl)isocyanuric acid is used as a triol compound having an isocyanuric ring, and the carboxylic acid is in the ortho position. A polyester polyol compound having an isocyanuric ring using an aromatic polycarboxylic acid substituted with orthophthalic anhydride as its anhydride and ethylene glycol as a polyhydric alcohol has particularly excellent oxygen barrier properties and adhesive properties. preferable.

The isocyanuric ring is highly polar and trifunctional, and can increase the polarity of the entire system and the crosslink density. From this point of view, it is preferable that the isocyanuric ring is contained in an amount of 5% by mass or more based on the total solid content of the adhesive resin.

The isocyanate compound has two or more isocyanate groups in the molecule.
Further, the isocyanate compound may be aromatic or aliphatic, and may be a low molecular compound or a high molecular compound.
Furthermore, the isocyanate compound may be a blocked isocyanate compound obtained by addition reaction using a known isocyanate blocking agent by a known and commonly used method.
Among these, from the viewpoint of adhesiveness and retort resistance, polyisocyanate compounds having three or more isocyanate groups are preferred, and from the viewpoint of oxygen barrier properties and water vapor barrier properties, aromatic compounds are preferred.

Specific isocyanate compounds include, for example, tetramethylene diisocyanate, hexamethylene diisocyanate, toluene diisocyanate, diphenylmethane diisocyanate, hydrogenated diphenylmethane diisocyanate, metaxylylene diisocyanate, hydrogenated xylylene diisocyanate, isophorone diisocyanate, and these isocyanate compounds. and adducts, burettes, and allophanates obtained by reacting these isocyanate compounds with low-molecular active hydrogen compounds or their alkylene oxide adducts, or high-molecular active hydrogen compounds.
Examples of low-molecular active hydrogen compounds include ethylene glycol, propylene glycol, metaxylylene alcohol, 1,3-bishydroxyethylbenzene, 1,4-bishydroxyethylbenzene, trimethylolpropane, glycerol, pentaerythritol, erythritol, sorbitol, Examples of the molecularly active hydrogen compounds include ethylenediamine, monoethanolamine, diethanolamine, triethanolamine, metaxylylenediamine, and the like, and examples of molecularly active hydrogen compounds include polymeric active hydrogen compounds of various polyester resins, polyether polyols, and polyamides.

The phosphoric acid modified compound is, for example, a compound represented by the following general formula (5) or (6).
In the general formula (5), R ₁ , R ₂ , and R ₃ are a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, a (meth)acryloyl group, a phenyl group that may have a substituent, and (meth)acryloyl The group is selected from alkyl groups having 1 to 4 carbon atoms and having an oxy group, at least one of which is a hydrogen atom, and n represents an integer of 1 to 4.
In the formula, R ₄ and R ₅ are a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, a (meth)acryloyl group, a phenyl group which may have a substituent, and a (meth)acryloyloxy group having 1 carbon number. A group selected from ~4 alkyl groups, where n is an integer of 1 to 4, x is an integer of 0 to 30, and y is an integer of 0 to 30, except when x and y are both 0. .

More specifically, phosphoric acid, pyrophosphoric acid, triphosphoric acid, methyl acid phosphate, ethyl acid phosphate, butyl acid phosphate, dibutyl phosphate, 2-ethylhexyl acid phosphate, bis(2-ethylhexyl) phosphate, isododecyl acid phosphate, butoxy Examples include ethyl acid phosphate, oleyl acid phosphate, tetracosyl acid phosphate, 2-hydroxyethyl methacrylate acid phosphate, and polyoxyethylene alkyl ether phosphate, and one or more of these can be used.

The content of the phosphoric acid modified compound in the resin composition is preferably 0.005% by mass or more and 10% by mass or less, and more preferably 0.01% by mass or more and 1% by mass or less.
By setting the content of the phosphoric acid-modified compound to 0.005% by mass or more, the oxygen barrier properties and water vapor barrier properties of the packaging material laminate of the present invention can be improved. Furthermore, by controlling the content of the phosphoric acid modified compound to 10% by mass or less, the adhesiveness of the adhesive layer can be improved.

The resin composition containing a polyester polyol, an isocyanate compound, and a phosphoric acid-modified compound may also contain a plate-like inorganic compound, which can improve the adhesiveness of the adhesive layer. Moreover, the bending load resistance of the laminate for packaging materials of the present invention can be improved.
Examples of platy inorganic compounds include kaolinite-serpentinite clay minerals (halloysite, kaolinite, endellite, dickite, nacrite, antigorite, chrysotile, etc.) and pyrophyllite-talc group (pyrophyllite, talc, Kerolai, etc.).

Examples of the coupling agent include a silane coupling agent represented by the following general formula (7), a titanium coupling agent, and an aluminum coupling agent. Note that these coupling agents may be used alone or in combination of two or more.

Examples of the silane coupling agent include vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, and γ-glycidoxypropyltrimethoxysilane. - Glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropyltriethoxysilane, γ-methacryloxytrimethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryloxy Propylmethyldiethoxysilane, γ-methacryloxypropyltriethoxysilane, N-β(aminoethyl)γ-aminopropylmethyldimethoxysilane, N-β(aminoethyl)γ-aminopropyltrimethoxysilane, N-β(aminoethyl)γ-aminopropyltrimethoxysilane, ethyl) γ-aminopropyltriethoxysilane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, γ-chloropropyltrimethoxysilane, γ-mercaptopropyl Examples include trimethoxysilane, 3-isocyanatepropyltriethoxysilane, 3-acryloxypropyltrimethoxysilane and 3-triethoxysilyl-N-(1,3-dimethyl-butylidene).

Examples of titanium-based coupling agents include isopropyl triisostearoyl titanate, isopropyl tri(N-aminoethyl-aminoethyl) titanate, isopropyl tridodecylbenzenesulfonyl titanate, isopropyl tris(dioctylpyrophosphate) titanate, and tetraoctyl bis (didodecyl phosphite) titanate, tetraoctyl bis(ditridecyl phosphite) titanate, bis(dioctyl pyrophosphate) oxyacetate titanate, bis(dioctyl pyrophosphate) ethylene titanate, isopropyltrioctaynortitanate, isopropyl dimethacrylic isostearoyl titanate , isopropyl isostearoyl diacryl titanate, diisostearoyl ethylene titanate, isopropyl tri(dioctyl phosphate) titanate, isopropyl tricumylphenyl titanate, and dicumylphenyloxyacetate titanate.

Specific examples of aluminum-based coupling agents include acetoalkoxyaluminum diisopropylate, diisopropoxyaluminum ethyl acetoacetate, diisopropoxyaluminum monomethacrylate, isopropoxyaluminum alkyl acetoacetate mono(dioctyl phosphate), aluminum Examples include -2-ethylhexanoate oxide trimer, aluminum stearate oxide trimer, and alkyl acetoacetate aluminum oxide trimer.

The resin composition can contain cyclodextrin and/or a derivative thereof, thereby improving the adhesiveness of the adhesive layer. Moreover, the bending load resistance of the laminate for packaging materials of the present invention can be further improved.
Specifically, for example, cyclodextrins such as cyclodextrins, alkylated cyclodextrins, acetylated cyclodextrins, and hydroxyalkylated cyclodextrins in which the hydrogen atoms of the hydroxyl groups of the glucose units of cyclodextrins are replaced with other functional groups may be used. I can do it. Branched cyclic dextrins can also be used.
In addition, the cyclodextrin skeleton in cyclodextrin and cyclodextrin derivatives includes α-cyclodextrin consisting of 6 glucose units, β-cyclodextrin consisting of 7 glucose units, and γ-cyclodextrin consisting of 8 glucose units. It may be either.
These compounds may be used alone or in combination of two or more. Further, these cyclodextrins and/or their derivatives may be hereinafter collectively referred to as dextrin compounds.

From the viewpoint of compatibility and dispersibility in the resin composition, it is preferable to use a cyclodextrin derivative as the cyclodextrin compound.

Examples of the alkylated cyclodextrin include methyl-α-cyclodextrin, methyl-β-cyclodextrin, and methyl-γ-cyclodextrin. These compounds may be used alone or in combination of two or more.

Examples of the acetylated cyclodextrin include monoacetyl-α-cyclodextrin, monoacetyl-β-cyclodextrin, and monoacetyl-γ-cyclodextrin. These compounds may be used alone or in combination of two or more.

Examples of the hydroxyalkylated cyclodextrin include hydroxypropyl-α-cyclodextrin, hydroxypropyl-β-cyclodextrin, and hydroxypropyl-γ-cyclodextrin. These compounds may be used alone or in combination of two or more.

The thickness of the adhesive layer is preferably 0.5 μm or more and 6 μm or less, more preferably 0.8 μm or more and 5 μm or less, and even more preferably 1 μm or more and 4.5 μm or less.
By setting the thickness of the adhesive layer to 0.5 μm or more, the adhesiveness of the adhesive layer can be improved. Furthermore, when a cured product of a resin composition containing a polyester polyol, an isocyanate compound, and a phosphoric acid modified compound is used, the bending load resistance of the laminate for packaging material can be improved.
By setting the thickness of the adhesive layer to 6 μm or less, the processing suitability of the packaging material laminate can be improved.

The adhesive layer is applied onto the base material or the heat seal layer by a conventionally known method such as a direct gravure roll coating method, a gravure roll coating method, a kiss coating method, a reverse roll coating method, a Fontaine method, and a transfer roll coating method, and is dried. It can be formed by

(heat seal layer)
The heat seal layer includes a second vapor deposited film and a polyolefin resin layer.

The present invention is characterized in that the thickness of the second vapor deposited film is smaller than the thickness of the polyolefin resin layer. With such a configuration, the recyclability of the packaging material laminate of the present invention can be improved.
The thickness of the second vapor deposited film is preferably smaller than the thickness of the polyolefin resin layer by 5 μm or more, more preferably by 10 μm or more. When the thickness of the second vapor-deposited film is 5 μm or more smaller than the thickness of the polyolefin resin layer, the recyclability of the packaging material laminate of the present invention can be further improved.

(Second vapor deposited film)
The heat seal layer of the present invention includes a second vapor deposited film on the polyolefin resin layer. Thereby, the oxygen barrier properties and water vapor barrier properties of the laminate for packaging materials of the present invention can be further improved.

The second vapor deposited film is made of a metal such as aluminum, and an inorganic oxide such as aluminum oxide, silicon oxide, magnesium oxide, calcium oxide, zirconium oxide, titanium oxide, boron oxide, hafnium oxide, barium oxide, etc. A vapor deposited film can be mentioned.

Further, the thickness of the second vapor deposited 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 setting the thickness of the second vapor-deposited film to 1 nm or more, the oxygen barrier properties and water vapor barrier properties of the packaging material laminate of the present invention can be further improved. Further, by setting the thickness of the second vapor deposited film to 150 nm or less, it is possible to prevent the occurrence of cracks in the second vapor deposited film, and to improve the recyclability of the laminate for packaging materials of the present invention. I can do it.

In order for the second vapor deposited film to be an aluminum vapor deposited film, the OD value thereof is preferably 2 or more and 3.5 or less. Thereby, it is possible to improve the oxygen barrier properties and water vapor barrier properties while maintaining the productivity of the laminate for packaging materials of the present invention. In the present invention, the OD value can be measured in accordance with JIS-K-7361.

The second vapor deposited film can be formed by the same method as the first vapor deposited film.

The surface of the second vapor deposited film is preferably subjected to the above surface treatment. Thereby, adhesion between adjacent layers can be improved.

(Polyolefin resin layer)
The polyolefin resin layer is characterized in that it is made of the same polyolefin as the polyolefin that constitutes the base material body described above. With such a configuration, it is possible to make the packaging material recyclable while maintaining its strength and heat resistance as a packaging material. However, the polyolefin resin layer is formed from an unstretched polyolefin resin film, or a heat seal layer is formed by melt extrusion.

Further, when polypropylene is used as the polyolefin resin layer, a heat seal modifier can be included in order to improve heat sealability. The heat seal modifier is not particularly limited as long as it has excellent compatibility with the polyolefin constituting the polyolefin resin layer, and examples thereof include olefin copolymers.

The thickness of the polyolefin resin layer is preferably 5 μm or more and 100 μm or less, more preferably 10 μm or more and 50 μm or less.
By setting the thickness of the polyolefin resin layer to 5 μm or more, the heat sealability and recyclability of the polyolefin resin layer can be improved. Further, by setting the thickness of the polyolefin resin layer to 100 μm or less, the processability of the laminate for packaging materials of the present invention can be improved.

In one embodiment, the polyolefin resin layer may have a multilayer structure. In particular, when a heat-sealing modifier is added to polypropylene as a polyolefin resin layer, the modifier may migrate (leach) to the gas barrier resin layer side. In this structure, the side to be heat sealed (the innermost layer side of the laminate) can be a layer containing a polyolefin resin and a heat seal modifier, and the outer layer can be a layer made of polypropylene. That is, examples of the multilayer structure include a multilayer structure consisting of a first polyolefin resin layer made of polyolefin and a second polyolefin resin layer made of polyolefin and a heat seal modifier.

The content of the heat seal modifier in the second polyolefin resin layer is preferably 10% by mass or more and 50% by mass or less, more preferably 20% by mass or more and 40% by mass or less.
By setting the content of the heat seal modifier in the second polyolefin resin layer to 10% by mass or more, the heat sealability of the second polyolefin resin layer can be improved. Further, by controlling the content of the heat seal modifier in the second polyolefin resin layer to 50% by mass or less, the recyclability of the laminate for packaging materials of the present invention can be improved.

Further, when the polyolefin resin layer has the above two-layer structure, the thickness of the first polyolefin resin layer is preferably 5 μm or more and 50 μm or less, more preferably 7 μm or more and 45 μm or less.
By setting the thickness of the first polyolefin resin layer to 5 μm or more, the recyclability of the packaging material laminate of the present invention and the heat sealability of the first polyolefin resin layer can be improved. Further, by setting the thickness of the first heat-sealing layer to 50 μm or less, the processing suitability of the laminate for packaging materials of the present invention can be improved.
Further, the thickness of the second polyolefin resin layer is preferably 5 μm or more and 20 μm or less, more preferably 7 μm or more and 15 μm or less.
By setting the thickness of the second polyolefin resin layer to 5 μm or more, the heat sealability of the second polyolefin resin layer can be improved. Further, by setting the thickness of the second polyolefin resin layer to 20 μm or less, it is possible to achieve both recyclability and processability of the laminate for packaging materials of the present invention.

(packaging material)
The packaging material of the present invention is characterized in that it is composed of the above packaging material laminate.
The shape of the packaging material is not particularly limited, and as shown in FIG. 4, it may have a bag-like shape.

In one embodiment, the bag-shaped packaging material can be manufactured by folding the laminate of the present invention in half and stacking them on top of each other so that the heat-sealing layer is on the inside, and heat-sealing the ends. .
In another embodiment, the bag-shaped packaging material can also be manufactured by stacking two laminates so that the heat-sealing layers face each other and heat-sealing the ends.
Note that in the figure, the shaded area represents the heat-sealed area.

The method of heat sealing is not particularly limited, and for example, known methods such as bar sealing, rotating roll sealing, belt sealing, impulse sealing, high frequency sealing, and ultrasonic sealing can be used.

Also, in one embodiment, the packaging material has a stand-up pouch shape with a body and a bottom, as shown in FIG.

For the stand pouch-shaped packaging material, the body is formed by heat-sealing the laminate into a cylinder so that the heat-sealing layer of the laminate is on the inside, and then another laminate is heat-sealed. The bottom part can be formed and manufactured by folding the body into a V-shape so that the layers are on the inside, sandwiching it from one end of the body, and heat-sealing it.

The contents filled in the packaging material are not particularly limited, and the contents may be liquid, powder, or gel. Moreover, it may be food or non-food.
After filling the contents, the opening can be heat-sealed to form a package.

EXAMPLES Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these Examples.

Example 1
A biaxially stretched polypropylene film (manufactured by Toyobo Co., Ltd., trade name: P2108) with a thickness of 18 μm is prepared as the base material main body, and a first vapor-deposited film with a thickness of A 30 nm thick aluminum oxide vapor deposited film was formed.

Furthermore, a polyvinyl alcohol barrier coating agent (manufactured by Michelman Co., Ltd., MFB7010) was coated on the aluminum oxide vapor-deposited film by a gravure method and dried to form a barrier coating layer with a thickness of 1 μm, thereby producing a base material.

An image was formed on the barrier coat layer of the base material formed as described above by a gravure printing method using a solvent-type gravure ink (manufactured by DIC Graphics Co., Ltd., Finart).

Polypropylene (manufactured by TPC Corporation, trade name: FL7540L, density: 0.90 g/cm ³ , melting point: 138°C, MFR: 7.0 g/10 minutes) was extruded into a film with a thickness of 35 μm using the T-die method. An unstretched polypropylene film was produced.

On one side of the unstretched polypropylene film produced as described above, a second vapor-deposited film, an aluminum vapor-deposited film having a thickness of 30 nm, was formed by PVD to produce a heat-sealing layer. In addition, when the vapor deposition concentration (OD value) of the formed vapor deposition film was measured, it was 3.0.

The barrier coat layer forming surface of the base material and the aluminum vapor deposited film forming surface of the heat seal layer are bonded together using a two-component curing polyurethane adhesive (manufactured by Rock Paint Co., Ltd., trade name: RU-3600/H-689). The laminate for packaging material of the present invention was obtained. The proportion of the same polyolefin (PP) in the packaging material laminate thus obtained was 93% by mass.

Example 2
A laminate for packaging materials of the present invention was produced in the same manner as in Example 1, except that the thickness of the aluminum vapor-deposited film was changed to 20 nm and the OD value of the vapor-deposited film was changed to 2.0. The proportion of the same polyolefin (PP) in the packaging material laminate thus obtained was 93% by mass.

Example 3
A laminate for packaging materials of the present invention was produced in the same manner as in Example 1, except that the barrier coat layer was not provided on the base material. The proportion of the same polyolefin (PP) in the packaging material laminate thus obtained was 95% by mass.

Example 4
The two-component curable polyurethane adhesive was replaced with a two-component curable adhesive containing a polyester polyol, an isocyanate compound, and a phosphoric acid modified compound (manufactured by DIC Corporation, product name: PASLIM).
A laminate for packaging material of the present invention was produced in the same manner as in Example 1, except that the laminate was changed to VM001/VM102CP). The proportion of the same polyolefin (PP) in the packaging material laminate thus obtained was 93% by mass.

Comparative example 1
A laminate for packaging material was obtained in the same manner as in Example 1, except that an unstretched polypropylene film (manufactured by Toyobo Co., Ltd., trade name: P1108) having a thickness of 18 μm was used as the base material body.
The proportion of the same polyolefin (PP) in the laminate thus obtained was 93% by mass.

Comparative example 2
A laminate for packaging material was obtained in the same manner as in Example 1 except that the first vapor deposited film was not provided.
The proportion of the same polyolefin (PP) in the laminate thus obtained was 93% by mass.

Comparative example 3
A laminate for packaging material was obtained in the same manner as in Example 1, except that the base material body was a biaxially stretched polyester film (manufactured by Toyobo Co., Ltd., trade name: E5100) having a thickness of 12 μm. The proportion of the same polyolefin (PP) in the laminate thus obtained was 69% by mass.

<<Recyclability evaluation>>
The recyclability of the packaging material laminates obtained in the above Examples and Comparative Examples was evaluated based on the following evaluation criteria. The evaluation results are summarized in Table 1.
(Evaluation criteria)
Good: The content of the same polyolefin in the packaging material laminate was 80% by mass or more.
×: The content of the same polyolefin in the laminate for packaging material was less than 80% by mass.

<<Strength evaluation>>
The strength of the packaging material laminates produced in the above Examples and Comparative Examples when pierced with a needle having a diameter of 0.5 mm was measured using a tensile tester (manufactured by Orientech, trade name: RTC-1310A). Note that the piercing speed was 50 mm/min. The measurement results are summarized in Table 1.

<<Heat resistance evaluation>>
Two test pieces each measuring 80 mm in length and 80 mm in width were prepared from the packaging material laminates obtained in the above Examples and Comparative Examples.
Two test pieces were stacked on top of each other so that the heat-sealing layers faced each other, and three sides were heat-sealed at 150° C. to produce a pouch-shaped packaging material.
The produced packaging material was visually observed, and the heat resistance of the packaging material laminate was evaluated based on the following evaluation criteria. The evaluation results are summarized in Table 1.
(Evaluation criteria)
○: No wrinkles were observed on the surface of the packaging material, and no adhesion to the heat seal bar was observed.
×: Wrinkles, etc. were generated on the surface of the packaging material, and adhesion to the heat seal bar was observed, so bag making could not be performed.

<<Oxygen barrier evaluation>>
The laminates for packaging materials obtained in the above Examples and Comparative Examples were cut into A4 size, and oxygen permeability (cc /m ² /day/atm) was measured. The measurement results are summarized in Table 1.

<<Water vapor barrier evaluation>>
The laminates for packaging materials obtained in the above Examples and Comparative Examples were cut into A4 size, and using PERMATRAN 3/31 manufactured by MOCON, USA, the water vapor permeability (g /m ² /day/atm) was measured. The measurement results are summarized in Table 1.

<Bending load resistance evaluation>
The laminate for packaging material obtained above was subjected to bending load (stroke: 155 mm, bending motion: 440 °) was given 5 times.
After the bending load, the oxygen permeability and water vapor permeability of the packaging material laminate were measured. The measurement results are summarized in Table 1.

<<Heat sealability test>>
Sample pieces were prepared by cutting the packaging material laminates obtained in the above examples and comparative examples into 10 cm x 10 cm pieces. This sample piece was folded in half so that the heat-sealing layer was on the inside, and an area of 1 cm x 10 cm was heat-sealed at a temperature of 150° C., a pressure of 1 kgf/cm ² , and a duration of 1 second.
The heat-sealed sample piece was cut into strips with a width of 15 mm, both ends that were not heat-sealed were held in a tensile tester, and the peel strength (N/15 mm) was measured at a speed of 300 mm/min and a load range of 50 N. It was measured. The measurement results are summarized in Table 1.
Note that the packaging material laminate obtained in Comparative Example 1 adhered to the heat seal bar and the peel strength could not be measured, so it was given a "-" rating.

10: Laminate for packaging material, 11: Base material main body, 12: First vapor deposited film, 13: Base material, 14: Adhesive layer, 15: Second vapor deposited film, 16: Polyolefin resin layer, 17: Heat seal layer, 18: barrier coat layer, 19: first polyolefin resin layer, 20: second polyolefin resin layer

Claims (5)

Comprising at least a base material, an adhesive layer, and a heat seal layer,
The base material includes a base material main body and a first vapor deposited film,
The heat-sealing layer includes a second vapor-deposited film and a polyolefin resin layer,
The base material body is a stretched resin film made of polyolefin,
The polyolefin constituting the base material body and the polyolefin constituting the polyolefin resin layer of the heat seal layer are the same polyolefin,
The thickness of the first vapor deposited film is smaller than the thickness of the base material body,
A laminate for packaging material, wherein the thickness of the second vapor-deposited film is smaller than the thickness of the polyolefin resin layer. The laminate for packaging material according to claim 1, wherein the base material further includes a barrier coat layer on the first vapor-deposited film. The second vapor deposited film is an aluminum vapor deposited film,
The laminate for packaging materials according to claim 1 or 2, wherein the adhesive layer includes a cured product of a resin composition containing a polyester polyol, an isocyanate compound, and a phosphoric acid modified compound. The laminate for packaging materials according to any one of claims 1 to 3, wherein the content of the polyolefin in the entire laminate for packaging materials is 80% by mass or more. A packaging material comprising the packaging material laminate according to any one of claims 1 to 4.