Patent Application
20230271760
The present invention relates to a gas barrier laminate and a packaging bag.
In many fields such as foods, beverages, pharmaceuticals, and chemicals, various packaging materials are used according to the contents of each product. Packaging materials are required to have properties for preventing transmission of oxygen, water vapor, and the like (gas barrier properties), which cause degeneration of the contents.
In recent years, in view of growing environmental awareness stemming from marine plastic debris problems and the like, the momentum toward plastic reduction is building up. From the viewpoint of reducing the amount of use of plastic materials, it has been investigated to use paper instead of plastic materials in a variety of fields. For example, in the following Patent Literature 1, a gas barrier laminate in which barrier layers are laminated on paper is disclosed.
Patent Literature 1: Japanese Unexamined Patent Publication No. 2020-69783
Since paper has crease retaining properties (also referred to as dead holding properties), paper has a feature that processing is easy. However, according to an investigation of the inventors of the present invention, it has been found that in a case where packaging bags having more acute-angled creases (pillow packaging, three-sided seal packaging, and gusset packaging) are used, there is still room for improvement from the viewpoint that cracks are generated in the barrier layer so that the gas barrier properties are deteriorated.
Furthermore, from the viewpoint of the Law for Promotion of Effective Utilization of Resources, it has been required to reduce the amount of use of plastic materials even in gas barrier laminates.
The present invention was achieved in view of the above-described circumstances, and it is an object of the invention to provide a gas barrier laminate that has crease retaining properties, which is a feature of paper, has sufficient gas barrier properties even after being folded, and contributes to a reduction in the amount of use of plastic materials, and to provide a packaging bag including this gas barrier laminate.
The present invention provides a gas barrier laminate including: a paper substrate; a layer including a polyvinyl alcohol-based resin; a vapor-deposited layer; and a layer including a polyolefin having a polar group, in order.
A polyolefin having a polar group may have at least one selected from a carboxyl group, a salt of a carboxyl group, a carboxylic acid anhydride, and a carboxylic acid ester.
The polyolefin having a polar group may be a copolymer of an acrylic acid ester and maleic anhydride.
The polyolefin having a polar group may be an ethylene-vinyl acetate copolymer.
The polyolefin having a polar group may be an ethylene-glycidyl methacrylate copolymer.
A thickness of the layer including a polyvinyl alcohol-based resin may be 1 µm or more and 5 µm or less.
A thickness of the vapor-deposited layer may be 30 nm or more and 100 nm or less.
A thickness of the layer including a polyolefin having a polar group may be 2 µm or more and 10 µm or less.
A thickness of the paper substrate may be 30 µm or more and 100 µm or less, and the thickness of the paper substrate may be 70% or more of the thickness of the entire gas barrier laminate.
A weight of paper may be 50% by mass or more based on the entire gas barrier laminate.
The present invention also provides a packaging bag including the above-described gas barrier laminate according to the present invention.
The packaging bag may have a folding part.
According to the present invention, a gas barrier laminate that has crease retaining properties, which is a feature of paper, has sufficient gas barrier properties even after being folded, and contributes to a reduction in the amount of use of plastic materials, and a packaging bag including this gas barrier laminate can be provided.
Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings as necessary. However, the present invention is not intended to be limited to the following embodiments.
The paper substrate 1 is not particularly limited and may be appropriately selected according to the use application of the packaging bag to which the gas barrier laminate 10 is applied. The paper substrate 1 is not particularly restricted as long as it is a paper containing plant-derived pulp as a main component. Specific examples of the paper substrate 1 include high-quality paper, special high-quality paper, coated paper, art paper, cast coated paper, imitation vellum paper, kraft paper, and glassine paper. The thickness of the paper substrate 1 may be, for example, 30 µm or more and 100 µm or less and may be 30 µm or more and 70 µm or less. Furthermore, the thickness of the paper substrate may be 70% or more of the thickness of the entire gas barrier laminate. When the thickness of the paper substrate is 70% or more of the thickness of the entire gas barrier laminate, it can be said that the gas barrier laminate has excellent environmental suitability.
The paper substrate 1 may be provided with at least a coat layer on the side that is in contact with the layer 2 including a polyvinyl alcohol-based resin that will be described below. By providing a coat layer, the layer 2 including a polyvinyl alcohol-based resin can be prevented from sinking into the paper, and the coat layer can accomplish a role of a sealer embedding the surface unevenness of the paper so that the layer including a polyvinyl alcohol-based resin can be uniformly formed without defects. In the coat layer, for example, various copolymers such as a styrene-butadiene-based copolymer, a styrene-acrylic copolymer, and an ethylene-vinyl acetate-based copolymer; a polyvinyl alcohol-based resin, a cellulose-based resin, and paraffin (WAX) are used as binder resins, and for example, clay, kaolin, calcium carbonate, talc, and mica may be included as fillers.
The thickness of the coat layer is not particularly restricted; however, the thickness may be, for example, 1 to 10 µm or 3 to 8 µm.
The weight of the paper is preferably 50% by mass or more, more preferably 70% by mass or more, and even more preferably 80% by mass or more, based on the entire gas barrier laminate. When the weight of the paper is 50% by mass or more based on the entire gas barrier laminate, the amount of use of plastic materials can be sufficiently reduced, the gas barrier laminate can be said to be made of paper on the whole, and at the same time, excellent recyclability is obtained.
The layer 2 including a polyvinyl alcohol-based resin is provided on the surface of the paper substrate and is provided for the purpose of improving the adhesiveness between the paper substrate 1 and the vapor-deposited layer 3 that will be described below or improving the gas barrier properties (particularly oxygen barrier properties) of the gas barrier laminate. The polyvinyl alcohol-based resin is, for example, a completely saponified polyvinyl alcohol resin, a partially saponified polyvinyl alcohol resin, a modified polyvinyl alcohol resin, or an ethylene-vinyl alcohol copolymer resin. Furthermore, the degree of polymerization of the polyvinyl alcohol-based resin is preferably 300 or higher and 1700 or less. When the degree of polymerization is 300 or higher, the barrier properties and bending resistance of the gas barrier laminate become satisfactory, and when the degree of polymerization is 1700 or less, the viscosity of the coating liquid of the polyvinyl alcohol-based resin that will be described below is lowered, and the coating properties become satisfactory.
Regarding a method for providing the layer 2 including a polyvinyl alcohol-based resin, the layer 2 including a polyvinyl alcohol-based resin can be obtained by applying a coating liquid including the above-mentioned polyvinyl alcohol-based resin and a solvent on the paper substrate 1 and drying the coating liquid. Examples of the solvent that is included in the coating liquid include water, methyl alcohol, ethyl alcohol, isopropyl alcohol, n-propyl alcohol, n-butyl alcohol, n-pentyl alcohol, dimethyl sulfoxide, dimethylformamide, and dimethylacetamide, and particularly a mixed solvent of water and an alcohol such as methyl alcohol, ethyl alcohol, or isopropyl alcohol is preferable. Furthermore, the coating liquid may also include additives such as a surfactant, an antiseptic agent, a storage stabilizer, a silane coupling agent, and an organic titanate.
Such a layer 2 including a polyvinyl alcohol-based resin has excellent pliability, can suppress cracks in the vapor-deposited layer that will be described below after bending (after folding) to suppress deterioration of the gas barrier properties, and at the same time, can improve the adhesiveness between the vapor-deposited layer and the layer including a polyvinyl alcohol-based resin.
The thickness of the layer 2 including a polyvinyl alcohol-based resin may be, for example, 1 µm or more, may be 2 µm or more, and may be 5 µm or less. When the thickness is 1 µm or more, the above-mentioned surface unevenness of the paper substrate can be efficiently embedded, and the vapor-deposited layer that will be described below can be uniformly laminated. Furthermore, when the thickness is 5 µm or less, the vapor-deposited layer can be uniformly laminated while the cost is suppressed.
The vapor-deposited layer 3 is a layer produced by vapor-depositing a metal or an inorganic compound. The vapor-deposited layer may be a layer obtained by vapor-depositing aluminum or may also include aluminum oxide (AlOx), silicon oxide (SiOx), and the like.
The thickness of the vapor-deposited layer 3 may be appropriately set according to the use application; however, the thickness may be preferably 30 nm or more or 50 nm or more and may be 100 nm or less or 80 nm or less. When the thickness of the vapor-deposited layer 3 is set to be 30 nm or more, sufficient continuity of the vapor-deposited layer 3 is likely to be obtained, and when the thickness is set to be 100 nm or less, generation of curls and cracks can be sufficiently suppressed, while sufficient gas barrier performance and flexibility are likely to be achieved.
It is preferable that the vapor-deposited layer 3 is formed by a vacuum film-forming means, from the viewpoints of oxygen gas barrier performance and film uniformity. Examples of the film-forming means include known methods such as a vacuum vapor deposition method, a sputtering method, and a chemical vapor deposition method (CVD method); however, from the viewpoint that the film-forming rate is fast and productivity is high, a vacuum vapor deposition method is preferable. Furthermore, among vacuum vapor deposition methods, particularly a film-forming means by electron beam heating is effective from the viewpoint that the film-forming rate is easily controlled by the area of irradiation, the electron beam current, and the like, and that temperature increase and temperature decrease to the vapor deposition material can be carried out in a short period of time.
The layer 4 including a polyolefin having a polar group is provided on the surface of the vapor-deposited layer 3 so as to be in contact with the vapor-deposited layer 3 and includes a polyolefin having a polar group. By using a polyolefin having a polar group, the water vapor barrier properties are improved by the crystallinity of the polyolefin, and at the same time, bending resistance is improved due to the pliability of the polyolefin. Furthermore, the adhesion to the vapor-deposited layer is improved by introducing a polar group, a water-based coating material in which the polyolefin is dispersed in water is obtained, which is favorable for the environment.
The polyolefin including a polar group may include a polyolefin having at least one selected from a carboxyl group, a salt of a carboxyl group, a carboxylic acid anhydride group, and a carboxylic acid ester.
As the polyolefin having a polar group, a product obtained by copolymerizing ethylene or propylene with an unsaturated carboxylic acid (an unsaturated compound having a carboxyl group, such as acrylic acid or methacrylic acid) or an unsaturated carboxylic acid ester, a salt obtained by neutralizing a carboxylic acid with a basic compound, or the like may be used, and in addition to those, products copolymerized with vinyl acetate, an epoxy-based compound, a chlorine-based compound, a urethane-based compound, a polyamide-based compound, with the like may also be used.
As the polyolefin having a polar group, specifically, a copolymer of an acrylic acid ester and maleic anhydride, an ethylene-vinyl acetate copolymer, an ethylene-glycidyl methacrylate copolymer, and the like may also be used.
Such a layer 4 including a polyolefin having a polar group has excellent pliability, can suppress cracks in the vapor-deposited layer after bending (after folding), and at the same time, has excellent adhesiveness to the vapor-deposited layer. In addition, by including the above-mentioned polyolefin, a gas barrier laminate having excellent water vapor barrier properties can be obtained. Furthermore, when a layer including the polyolefin having a polar group is provided, since the layer can also take a role as a heat seal layer, it is not necessary to provide a heat seal layer separately.
The layer 4 including a polyolefin having a polar group may include other components in addition to the above-described polyolefin. Examples of the other components include a silane coupling agent, an organic titanate, a polyacrylic, a polyester, a polyurethane, a polycarbonate, a polyurea, a polyamide, a polyolefin-based emulsion, a polyimide, melamine, and phenol.
The content of the polyolefin in the layer 4 including a polyolefin having a polar group may be, for example, 50% by mass or more, may be 70% by mass or more, may be 90% by mass or more, or may be 100% by mass.
The thickness of the layer 4 including a polyolefin having a polar group may be, for example, 2 µm or more, may be 3 µm or more, may be 10 µm or less, may be 8 µm or less, or may be 5 µm or less. When the thickness of the layer 4 including a polyolefin having a polar group is 2 µm or more, the role as the above-mentioned heat seal layer can be sufficiently exhibited. Furthermore, when the thickness of the layer 4 including a polyolefin having a polar group is 10 µm or less, the adhesiveness to the vapor-deposited layer and the barrier properties can be sufficiently exhibited while the cost is suppressed.
Regarding a method for providing the layer 4 including a polyolefin having a polar group, the layer 4 including a polyolefin having a polar group can be obtained by applying a coating liquid including the above-mentioned polyolefin and a solvent on the vapor-deposited layer and drying the coating liquid. Examples of the solvent that is included in the coating liquid include water, methyl alcohol, ethyl alcohol, isopropyl alcohol, n-propyl alcohol, n-butyl alcohol, n-pentyl alcohol, dimethyl sulfoxide, dimethylformamide, dimethylacetamide, toluene, hexane, heptane, cyclohexane, acetone, methyl ethyl ketone, diethyl ether, dioxane, tetrahydrofuran, ethyl acetate, and butyl acetate. Regarding these solvents, one kind thereof may be used alone, or two or more kinds thereof may be used in combination. Among these, from the viewpoint of characteristics, methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, ethyl acetate, methyl ethyl ketone, and water are preferable. Furthermore, from an environmental viewpoint, methyl alcohol, ethyl alcohol, isopropyl alcohol, and water are preferable.
The gas barrier laminate according to the present embodiment can exhibit sufficient gas barrier properties even after being folded. The gas barrier properties according to the present specification implies the water vapor transmission rate and oxygen transmission rate are sufficiently low.
With regard to the gas barrier laminate according to the present embodiment, it is preferable that the water vapor transmission rate at 40° C. and 90%RH obtained by folding the gas barrier laminate, with the paper substrate being placed on the outer side, rolling a roller having a weight of 600 g thereon one time, opening the fold, and making measurement, is 3 g/m2/d or less, and the oxygen transmission rate at 30° C. and 70%RH is 3 cc/m2/d/atm or less. Furthermore, it is preferable that the water vapor transmission rate at 40° C. and 90%RH obtained by placing the paper substrate on the inner side, rolling a roller having a weight of 600 g thereon one time, opening the fold, and making measurement, is 3 g/m2/d or less, and the oxygen transmission rate at 30° C. and 70%RH is 3 cc/m2/d/atm or less.
The packaging bag may be formed into a bag shape by folding one sheet of a gas barrier laminate in two such that the two parts of the layer 4 including a polyolefin having a polar group face each other, subsequently appropriately folding the gas barrier laminate into a desired shape, and then heat-sealing the resultant, or may be formed into a bag shape by superposing two sheets of a gas barrier laminate such that the layer 4 including a polyolefin having a polar group face each other, and then heat-sealing the gas barrier laminates.
With regard to the packaging bag according to the present embodiment, the heat seal strength may be 2 N or greater or may be 4 N or greater. Incidentally, the upper limit value of the heat seal strength is not particularly limited; however, the upper limit value may be, for example, 10 N or less.
Here, the heat seal strength is a value obtained by superposing two sheets of a gas barrier laminate 10 such that layers 4 including a polyolefin having a polar group face each other, performing heat sealing with a heat sealer under the conditions of 120° C., 0.2 MPa, and 1 second, cutting the resultant into a strip having a width of 15 mm, and measuring the maximum load when the strip is subjected to T-shape peeling at a peeling rate of 300 mm/min.
The packaging bag can accommodate contents such as foods and medicines as contents. Particularly, the packaging bag is suitable for accommodating confectionery and the like as foods. The packaging bag according to the present embodiment can maintain high gas barrier properties even when the packaging bag has a shape with folding parts.
Incidentally, in the present embodiment, a gusset bag has been mentioned as an example of the packaging bag; however, the gas barrier laminate according to the present embodiment may also be used to produce, for example, a pillow bag, a three-sided sealed bag, or a standing pouch.
Hereinafter, the present invention will be described in more detail by way of Examples; however, the present invention is not intended to be limited to these examples.
A coating liquid obtained by dissolving a polyvinyl alcohol resin having a degree of saponification of 98% and a degree of polymerization of 500 in a solution of water/IPA = 8/2 at a solid content concentration of 10% by mass, was applied on a clay coat surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including a polyvinyl alcohol resin. The thickness of the layer was 3 µm. Subsequently, AL vapor deposition was applied on the layer including a polyvinyl alcohol resin by a vacuum vapor deposition method. The thickness of the AL vapor-deposited layer was 50 nm. Thereafter, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on the vapor-deposited layer with a bar coater and was dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the thickness of the layer including a polyvinyl alcohol resin was set to 1 µm. The weight of paper in the gas barrier laminate was 85% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the thickness of the layer including a polyvinyl alcohol resin was set to 5 µm. The weight of paper in the gas barrier laminate was 79% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the thickness of the vapor-deposited layer was set to 30 nm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the thickness of the vapor-deposited layer was set to 100 nm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the thickness of the layer including a polyolefin having a polar group was set to 2 µm. The weight of paper in the gas barrier laminate was 83% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the thickness of the layer including a polyolefin having a polar group was set to 10 µm. The weight of paper in the gas barrier laminate was 73% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a clay-coated paper having a thickness of paper of 30 µm and a thickness of clay coat layer of 5 µm was used. The weight of paper in the gas barrier laminate was 73% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a clay-coated paper having a thickness of paper of 100 µm and a thickness of clay coat layer of 5 µm was used. The weight of paper in the gas barrier laminate was 90% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the vapor-deposited layer was formed with silica, and the thickness of the vapor-deposited layer was set to 30 nm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the vapor-deposited layer was formed with alumina, and the thickness of the vapor-deposited layer was set to 30 nm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a polyvinyl alcohol-based resin having a degree of saponification of 98% and a degree of polymerization of 1000 was used as the polyvinyl alcohol-based resin.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that the polyvinyl alcohol-based resin used in Example 1 was changed to a modified polyvinyl alcohol-based resin (trade name: EXCEVAL AQ4104, manufactured by Kuraray Co., Ltd.).
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a coating liquid including an ethylene-vinyl acetate copolymer resin (trade name: CHEMIPEARL V300, manufactured by Mitsui Chemicals, Inc.) was applied with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a coating liquid including a polyolefin resin including a carboxyl group, a salt of a carboxyl group, a carboxylic acid anhydride, and a carboxylic acid ester (trade name: BONDINE HX-8290, manufactured by Arkema S.A.) was applied with a bar coater and dried in an oven to produce a coating liquid layer formed from a polyolefin. Incidentally, the coating liquid including a polyolefin resin was prepared as follows.
A polyolefin resin composed of ethylene, ethyl acrylate, and maleic anhydride (trade name: BONDINE HX-8290, manufactured by Arkema S.A.), isopropanol, triethylamine, and distilled water were mixed at proportions of 20/20/1/59 in a mass ratio and then heated and stirred, and an aqueous dispersion of the polyolefin resin was prepared.
A gas barrier laminate was obtained in the same manner as in Example 1, except that a coating liquid of an ethylene-glycidyl methacrylate copolymer (trade name: SEPOLSION G515, manufactured by SUMITOMO CHEMICAL COMPANY, LIMITED) was applied with a bar coater and dried in an oven to produce a coating liquid layer including a polyolefin resin.
A coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on a clay coat surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including a polyolefin having a polar group. The thickness of the layer was 3 µm. Subsequently, a coating liquid obtained by dissolving a polyvinyl alcohol resin having a degree of saponification of 98% and a degree of polymerization of 500 in a solution of water/IPA = 8/2 at a solid content concentration of 10% by mass, was applied on the layer including a polyolefin having a polar group with a bar coater and was dried in an oven to form a layer including a polyvinyl alcohol resin. The thickness of the layer was 1 µm. Subsequently, AL vapor deposition was applied on the layer including a polyvinyl alcohol resin by a vacuum vapor deposition method. The thickness of the AL vapor-deposited layer was 50 nm. Subsequently, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on the vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 81% by mass.
A coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on a clay coat surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including a polyolefin having a polar group. The thickness of the layer was 3 µm. Subsequently, AL vapor deposition was applied on the layer including a polyvinyl alcohol resin by a vacuum vapor deposition method. The thickness of the AL vapor-deposited layer was 50 nm. Thereafter, a coating liquid obtained by dissolving a polyvinyl alcohol resin having a degree of saponification of 98% and a degree of polymerization of 500 in a solution of water/IPA = 8/2 at a solid content concentration of 10% by mass, was applied on the vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyvinyl alcohol resin. The thickness of the layer was 3 µm. Subsequently, AL vapor deposition was applied on the layer including a polyvinyl alcohol resin by a vacuum vapor deposition method. The thickness of the AL vapor-deposited layer was 50 nm. Thereafter, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on the vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 78% by mass.
A coating liquid including a polyolefin resin including a carboxyl group, a salt of a carboxyl group, a carboxylic acid anhydride group, and a carboxylic acid ester (refer to Example 15 for the preparation of the coating liquid) was applied on a clay coat surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including a polyolefin having polar groups. The thickness of the layer was 2 µm. Subsequently, a coating liquid obtained by dissolving a polyvinyl alcohol resin having a degree of saponification of 98% and a degree of polymerization of 500 in a solution of water/IPA = 8/2 at a solid content concentration of 10% by mass, was applied on the layer including a polyolefin having polar groups with a bar coater and was dried in an oven to form a layer including a polyvinyl alcohol resin. The thickness of the layer was 1 µm. Subsequently, AL vapor deposition was applied on the layer including a polyvinyl alcohol resin by a vacuum vapor deposition method. The thickness of the AL vapor-deposited layer was 50 nm. Subsequently, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on the vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 19, except that the polyvinyl alcohol resin was changed to a modified polyvinyl alcohol resin (trade name: EXCEVAL AQ4104, manufactured by Kuraray Co., Ltd.).
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a vapor-deposited layer was not provided. The weight of paper in the gas barrier laminate was 82% by mass.
A coating liquid including an acrylic alkyd resin was applied on the surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including an acrylic alkyd resin. The thickness of the layer was 4 µm. Subsequently, AL vapor deposition was applied on this layer. The thickness of the AL vapor-deposited layer was 50 nm. Thereafter, a coating liquid including a polyvinyl alcohol resin and TEOS was applied on the AL vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyvinyl alcohol resin and TEOS. The thickness of the layer was 0.4 µm. Thereafter, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 80% by mass.
A coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S100, manufactured by Mitsui Chemicals, Inc.) was applied on the surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including a polyolefin having a polar group. The thickness of the layer was 3 µm. Subsequently, AL vapor deposition was applied on the layer including a polyolefin having a polar group. The thickness of the AL vapor-deposited layer was 50 nm. Thereafter, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied on the vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a coating liquid including an ethylene-vinyl acetate copolymer resin (trade name: CHEMIPEARL V300, manufactured by Mitsui Chemicals, Inc.) was used instead of a coating liquid including a polyvinyl alcohol resin. The weight of paper in the gas barrier laminate was 82% by mass.
A gas barrier laminate was obtained by an operation similar to that in Example 1, except that a coating liquid including a urethane-curable acrylic resin was used instead of a coating liquid including a polyvinyl alcohol resin. The weight of paper in the gas barrier laminate was 82% by mass.
A coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S100, manufactured by Mitsui Chemicals, Inc.) was applied on the surface of paper (clay-coated paper, thickness of paper: 50 µm, thickness of clay coat layer: 5 µm) with a bar coater and was dried in an oven to form a layer including a polyolefin having a polar group. The thickness of the layer was 3 µm. Subsequently, AL vapor deposition was applied on the layer including a polyolefin having a polar group. The thickness of the AL vapor-deposited layer was 50 nm. Thereafter, a coating liquid including a polyvinyl alcohol resin was applied on the AL vapor-deposited layer with a bar coater and dried in an oven to form a layer including a polyvinyl alcohol resin. The thickness of the layer was 1 µm. Thereafter, a coating liquid including a salt of a carboxyl group (trade name: CHEMIPEARL S500, manufactured by Mitsui Chemicals, Inc.) was applied with a bar coater and dried in an oven to form a layer including a polyolefin having a polar group, and a gas barrier laminate was obtained. The thickness of the layer including a polyolefin having a polar group was 3 µm. The weight of paper in the gas barrier laminate was 81% by mass.
A gas barrier laminate was obtained by an operation similar to that in Comparative Example 6, except that a coating liquid including a polyvinyl alcohol resin and TEOS was applied with a bar coater and dried in oven to form a layer including a polyvinyl alcohol resin and TEOS, instead of applying a coating liquid including a polyvinyl alcohol resin with a bar coater, drying the coating liquid in an oven, and forming a layer including a polyvinyl alcohol resin. The thickness of this layer was 1 µm.
The water vapor transmission rates of the gas barrier laminates according to Examples and Comparative Examples were measured by a MOCON method. The measurement conditions were set to a temperature of 40° C. and a relative humidity of 90%. A gas barrier laminate was creased while a roller weighing 600 g was rolled at a rate of 300 mm/min, and the water vapor transmission rate of the gas barrier laminate after opening was also similarly measured. Incidentally, the term “inward folding” in Table 1 to Table 8 means a gas barrier laminate after mountain-folding the gas barrier laminate as viewed from the paper substrate side, and the term “outward folding” indicates a gas barrier laminate after valley-folding the gas barrier laminate as viewed from the paper substrate side. The results are expressed in the unit of [g/m2·day] in Table 1 to Table 8.
The oxygen transmission rates of the gas barrier laminates according to Examples and Comparative Examples were measured by JIS K7126, method B (isopiestic method). As the measurement apparatus, OXTRAN 2/20 manufactured by MOCON, Inc. was used, and measurement was made at a temperature of 30° C. and a relative humidity of 70%. The results are expressed in the unit of [cc/m2/d/atm] in Table 1 to Table 8.
Two sheets of a gas barrier laminate were superposed such that the layers including a polyolefin having a polar group faced each other, heat-sealing was performed with a heat sealer under the conditions of 120° C., 0.2 MPa, and 1 second, a strip having a width of 15 mm was cut out therefrom, and the maximum load when the strip was subjected to T-shape peeling at a peeling rate of 300 mm/min was measured. The results are expressed in the unit of [N/15 mm] in Table 1 to Table 8.
1: paper substrate, 2: layer including polyvinyl alcohol-based resin, 3: vapor-deposited layer, 4: layer including polyolefin having polar group, 10: gas barrier laminate, 20: gusset bag, B1, B2: folding part.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-118634 | Jul 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2022/022372 | 6/11/2021 | WO |
