JP6351308B2 - Laminate - Google Patents

Description

  The present invention relates to a laminate having a gas barrier property which is small in mechanical strength even after retorting and has excellent gas barrier properties even under high humidity.

  Plastic films such as polyamide films are excellent in strength, transparency and moldability, and are therefore used in a wide range of applications as packaging materials. When these plastic films are used for packaging retort-treated products such as foods containing moisture, gas barrier properties under high humidity and mechanical strength during retort treatment are required.

  As a method for imparting a gas barrier property under high humidity to a plastic substrate, for example, in Patent Document 1, a laminate comprising a plastic substrate, a gas barrier layer, and a polymer layer containing a divalent or higher-valent metal compound is added to water. A method of heat treatment in the presence of is described.

  However, in the method of Patent Document 1, after forming a gas barrier layer, pressure treatment using an autoclave is performed in water containing a metal compound, and it is difficult to carry out continuously, resulting in poor productivity. It was a thing. In Patent Document 1, a solvent-based paint is applied on a plastic substrate and dried to form an undercoat layer, and then a water-based paint is applied and dried to form a gas barrier layer. Therefore, the method of Patent Document 1 has problems in terms of economy and productivity, such as the need for an explosion-proof facility for using a solvent-based paint, and the need for multiple applications.

  However, in the method of Patent Document 1, after forming a gas barrier layer, pressure treatment using an autoclave is performed in water containing a metal compound, and it is difficult to carry out continuously, resulting in poor productivity. It was a thing. In Patent Document 1, the undercoat layer is formed by applying and drying a solvent-based paint, and then the gas barrier layer is formed by applying and drying a water-based paint. Therefore, the method of Patent Document 1 has problems in terms of economy and productivity, such as the need for an explosion-proof facility for using a solvent-based paint, and the need for multiple applications.

JP 2004-322626 A

  An object of the present invention is to provide a laminate that solves the above problems, is excellent in productivity and economy, has a small decrease in mechanical strength even when subjected to retort treatment, and has excellent gas barrier properties even under high humidity. With the goal.

  As a result of intensive studies on the above problems, the present inventor used a plastic substrate containing a specific amount of a metal compound and an antioxidant, and a laminate obtained by laminating a gas barrier layer containing a polycarboxylic acid on the plastic substrate. The present inventors have found that even when the treatment is performed, the decrease in mechanical strength is small and the gas barrier property is excellent even under high humidity, and the present invention has been achieved.

That is, the gist of the present invention is as follows.
(1) The gas barrier layer (II) is laminated on the plastic substrate (I), and the plastic substrate (I) contains 0.1 to 70 mass% of the metal compound and 0.03 to 0.1 of the antioxidant. Including a metal-containing layer containing by mass% ,
The gas barrier layer (II) contains a polycarboxylic acid ,
The metal-containing layer is obtained by extruding a melt of a thermoplastic resin in which a metal compound and an antioxidant are mixed.
The metal-containing layer and the layer (II) containing polycarboxylic acid are in contact;
After retorting at 130 ° C. for 30 minutes, the oxygen permeability under an atmosphere of 20 ° C. and 65% relative humidity is 150 mL / (m ² · day · MPa) or less.
The tensile strength retention before and after retorting at 130 ° C. for 30 minutes is 85% or more,
The plastic substrate (I) is stretched,
A laminate characterized by the above.
(2) The laminate according to (1), wherein the antioxidant is a hindered phenol-based antioxidant.
(3) The hindered phenol antioxidant is pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] or N, N′-hexamethylenebis ( The laminate according to (2), which is 3,5-di-t-butyl-4-hydroxy-hydrocinnamide).
(4) The laminate according to any one of (1) to (3), wherein the plastic substrate (I) is a multilayer film.
(5) The laminate according to any one of (1) to (4), wherein the gas barrier layer (II) contains a polyalcohol.
(6) The laminated body according to any one of (1) to (5), wherein the metal constituting the metal compound is one selected from magnesium, calcium, and zinc.
(7) Oxygen permeability under an atmosphere of 20 ° C. and a relative humidity of 65% after hydrothermal treatment at 95 ° C. for 30 minutes is 150 mL / (m ² · day · MPa) or less (1) to (6) The laminated body in any one of.
(8) A packaging bag comprising the laminate according to any one of (1) to (7) .

ADVANTAGE OF THE INVENTION According to this invention, it is excellent in productivity and economical efficiency, and even if it performs a retort process, the fall of mechanical strength is small, and the laminated body which has the outstanding gas barrier property also under high humidity can be provided.
Moreover, the laminated body containing a metal compound in the present invention can be produced simply by adding the metal compound to the raw material of the base material, and a conventional layer containing the metal compound is laminated on the base material. The process can be omitted. Therefore, a laminate can be obtained with a smaller number of processes than before, and therefore, industrial merit is extremely large from the viewpoint of productivity and cost.

Hereinafter, the present invention will be described in detail.
The laminate of the present invention is obtained by laminating a gas barrier layer (II) on a plastic substrate (I), and the plastic substrate (I) needs to contain a metal compound and an antioxidant.

  In the present invention, the plastic substrate (I) needs to contain a metal compound. The metal constituting the metal compound is not particularly limited, and monovalent metals such as lithium, sodium, potassium, rubidium, and cesium, and magnesium, calcium, zirconium, zinc, copper, cobalt, iron, nickel, aluminum, and the like. A bivalent or higher metal is mentioned. Among them, a metal having a high ionization tendency is preferable from the viewpoint of easy reaction with carboxylic acid, and a monovalent or divalent metal is preferable from the viewpoint of gas barrier properties. Specifically, lithium, sodium, potassium, magnesium, calcium, and zinc are preferable, and magnesium, calcium, and zinc are more preferable. The type of metal is not limited to one type, and may be two or more types.

  In the present invention, the metal compound is a compound containing the above metal, and examples of the compound include oxides, hydroxides, halides, inorganic salts such as carbonates, bicarbonates, phosphates, sulfates, Examples thereof include carboxylate such as acetate, formate, stearate, citrate, malate, and maleate, and organic acid salt such as sulfonate, and is preferably an oxide or carbonate. . Moreover, you may use a metal simple substance as a metal compound.

  Among the above metal compounds, preferred examples include lithium carbonate, sodium hydrogen carbonate, magnesium oxide, magnesium carbonate, magnesium hydroxide, magnesium acetate, calcium oxide, calcium carbonate, calcium hydroxide, calcium chloride, calcium phosphate, calcium sulfate, acetic acid. Calcium, zinc acetate, zinc oxide, zinc carbonate, etc. can be mentioned. From the viewpoint of gas barrier properties, magnesium salts such as magnesium oxide, magnesium carbonate, magnesium hydroxide, magnesium acetate, calcium carbonate, calcium acetate, zinc oxide, A divalent metal compound such as zinc acetate is preferable. From the viewpoint of the transparency of the plastic substrate (I), a monovalent compound such as lithium carbonate or sodium hydrogen carbonate, magnesium oxide, magnesium carbonate, magnesium hydroxide, etc. Magnesium salts are preferred. These may be used alone or in combination.

  The metal compound is preferably in a powder form, and the average particle diameter is not particularly limited, but is preferably 0.001 to 10.0 μm, more preferably 0.005 to 5.0 μm, and 0 The thickness is more preferably 0.01 to 2.0 μm, and particularly preferably 0.05 to 1.0 μm. Since the haze of the laminate can be reduced, the metal compound preferably has a smaller average particle size. However, a metal compound having an average particle size of less than 0.001 μm has a large surface area, so that it easily aggregates, and coarse aggregates are scattered in the film, which may deteriorate the mechanical properties of the substrate. On the other hand, when the metal compound contains a metal compound having an average particle size exceeding 10.0 μm, the frequency of breaking when the film is formed increases, and the productivity tends to decrease.

  A metal compound can improve dispersibility, weather resistance, wettability with a thermoplastic resin, heat resistance, transparency, and the like by performing surface treatment such as inorganic treatment or organic treatment. Examples of the inorganic treatment include alumina treatment, silica treatment, titania treatment, zirconia treatment, tin oxide treatment, antimony oxide treatment, and zinc oxide treatment. Examples of the organic treatment include treatment using a fatty acid compound, a polyol compound such as pentaerythritol and trimethylolpropane, an amine compound such as triethanolamine and trimethylolamine, a silicone compound such as a silicone resin and alkylchlorosilane. .

  The content of the metal compound in the plastic substrate (I) needs to be 0.1 to 70% by mass, preferably 0.1 to 50% by mass, and 0.2 to 20% by mass. More preferably, it is 0.2-5 mass%. From the viewpoint of haze, it is preferably less than 5% by mass. When the content of the metal compound in the plastic substrate (I) is 0.1 to 70% by mass, the obtained plastic substrate (I) can obtain excellent gas barrier properties. However, when the content of the metal compound in the polyimide film is less than 0.1% by mass, the crosslinked structure formed by reacting with the polycarboxylic acid of the gas barrier layer (II) is reduced, and the resulting plastic substrate ( The gas barrier property of I) is lowered. On the other hand, when the content exceeds 70% by mass, the frequency of breakage during stretching during film formation increases, productivity tends to decrease, and mechanical properties also tend to decrease.

  In the present invention, the plastic substrate (I) needs to contain an antioxidant. Examples of the antioxidant include hindered phenol antioxidants, sulfur antioxidants, and phosphorus antioxidants. Among them, hindered phenol antioxidants are preferable. As the hindered phenol-based antioxidant, pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] from the viewpoint of heat resistance and compatibility with polyamide resin, N, N′-hexamethylene bis (3,5-di-tert-butyl-4-hydroxy-hydrocinnamide) and mixtures thereof are preferred.

  The content of the antioxidant in the plastic substrate (I) is required to be 0.03 to 0.10% by mass, and preferably 0.06 to 0.10% by mass. When the content of the antioxidant in the plastic substrate (I) is 0.03 to 0.10% by mass, it is possible to suppress a decrease in strength of retort treatment of the obtained laminate. However, when the content of the antioxidant in the plastic substrate (I) is less than 0.03% by mass, the strength of the obtained laminate after the retort treatment is significantly reduced. On the other hand, if the content exceeds 0.10% by mass, not only is it uneconomical, but the slipperiness of the resulting laminate may be impaired.

  Examples of the thermoplastic resin constituting the plastic substrate (I) include polyolefin resins such as polyethylene, polypropylene, and ionomer, polyamide resins such as polyamide 6, polyamide 66, polyamide 46, and polyamide 9T, polyethylene terephthalate, polyethylene isophthalate, and polyethylene naphthalate. Phthalate, polytrimethylene terephthalate, polytrimethylene naphthalate, polybutylene terephthalate, polybutylene naphthalate, polyester resin such as polylactic acid, vinyl chloride, polystyrene resin, polycarbonate resin, polyarylate resin, ethylene-vinyl acetate copolymer, Examples thereof include an ethylene-vinyl alcohol copolymer or a mixture thereof. Of these thermoplastic resins, when a packaging bag is constructed, a polyamide resin is preferable because of excellent puncture strength and impact resistance, and a polyester resin is preferable because of excellent heat resistance and economy. .

  For thermoplastic resins, reinforcing materials, pigments, anti-degradation agents, weathering agents, flame retardants, plasticizers, preservatives, UV absorbers, antistatic agents, blocking as long as they do not adversely affect performance. You may add 1 type, or 2 or more types of various additives, such as an inhibitor. In addition, inorganic particles other than metal compounds and organic lubricants may be added to the thermoplastic resin for the purpose of improving the slip property of the film. Among them, silica is preferably added.

  A method for adding a metal compound, an antioxidant, or an additive to the thermoplastic resin is not particularly limited, and the thermoplastic resin can be blended at an arbitrary point in the manufacturing process. For example, a method of adding when polymerizing a thermoplastic resin, a method of kneading a thermoplastic resin and an additive in an extruder, or a master batch in which an additive is kneaded at a high concentration and blended is manufactured. Examples include a method of adding and diluting to a thermoplastic resin (master batch method). In the present invention, the master batch method is preferably employed.

  The thickness of the plastic substrate (I) can be appropriately selected according to the mechanical strength required for the obtained gas barrier laminate. For reasons of mechanical strength and ease of handling, the thickness of the plastic substrate (I) is preferably 5 to 100 μm, and more preferably 10 to 30 μm. If the thickness of the plastic substrate (I) is less than 5 μm, sufficient mechanical strength cannot be obtained, and the piercing strength tends to deteriorate.

  If the plastic substrate (I) contains a metal compound and an antioxidant, it may be a single-layer film or a multi-layer film, but if it is a multi-layer film, The at least one layer needs to contain 0.1 to 70% by mass of the metal compound. On the other hand, it is desirable that the antioxidant is added to all layers. Hereinafter, a layer containing 0.1 to 70% by mass of a metal compound in a multilayer film or a single layer film is referred to as a “metal-containing layer (M)”, and other than the “metal-containing layer (M)” in the multilayer film. This layer may be referred to as “resin layer (R)”.

  When the plastic substrate (I) is a multilayer film, the structure of the obtained plastic substrate (I) is that the gas barrier layer (II) and the metal-containing layer (M) of the plastic substrate (I) are in contact with each other. (R) / (M) / (II), (M) / (R) / (M) / (II), (II) / (M) / (R) / (M) / ( II) and the like. Since these structures are such that the gas barrier layer (II) and the metal-containing layer (M) are in contact with each other, the polycarboxylic acid in the gas barrier layer (II) and the metal compound in the metal-containing layer (M) are likely to react. Gas barrier properties can be obtained efficiently. Among these, in consideration of equipment for manufacturing and operability, the configuration of (R) / (M) / (II) is preferable. Further, the gas barrier layer (II) and the resin layer (R) are in contact with each other, (M) / (R) / (II), (R) / (M) / (R) / (II), ( II) / (R) / (M) / (R) / (II) and the like. Among these, the structure of (M) / (R) / (II) is preferable in consideration of equipment for manufacturing and operability.

  Although the thickness composition ratio of the metal-containing layer (M) and the resin layer (R) constituting the multilayer film is not particularly limited, the total thickness (Mt) of the metal-containing layer (M) and the total of the resin layer (R) The ratio of thickness (Rt) ((Rt) / (Mt)) is preferably 1/1000 to 1000/1, and the thickness control of each layer is easy, so 1/100 to 100/1. More preferably, it is more preferably 1/10 to 10/1.

  Antioxidants and the above-mentioned additives may be added to the resin layer (R), and it is preferable to add silica or the like to the resin layer (R) which is the outermost layer for the purpose of improving slip properties. .

  The gas barrier layer (II) constituting the laminate of the present invention needs to contain a polycarboxylic acid. The polycarboxylic acid in the gas barrier layer (II) can exhibit gas barrier properties by reacting with the metal compound in the plastic substrate (I).

  The polycarboxylic acid in the present invention is a compound or polymer having two or more carboxyl groups in the molecule, and these carboxyl groups may form an anhydride structure. Specific examples of the polycarboxylic acid include 1,2,3,4-butanetetracarboxylic acid, polyacrylic acid, polymethacrylic acid, acrylic acid-methacrylic acid copolymer, acrylic acid-maleic acid copolymer, polymaleic acid Examples thereof include olefin-maleic acid copolymers such as ethylene-maleic acid copolymers, polysaccharides having carboxyl groups in the side chains such as alginic acid, polyamides containing carboxyl groups, and polyesters. The said polycarboxylic acid may be used independently and may be used together.

  When the polycarboxylic acid is a polymer, the weight average molecular weight is preferably 1000 to 1000000, more preferably 10000 to 150,000, and further preferably 15000 to 110000. If the weight average molecular weight of the polycarboxylic acid is too low, the resulting gas barrier layer (II) becomes fragile. On the other hand, if the molecular weight is too high, the handling properties are impaired, and in some cases, the gas barrier layer (II) described later is used. The gas barrier layer (II) obtained by agglomeration in the coating liquid for forming may have a gas barrier property impaired.

  In the present invention, among the above polycarboxylic acids, polyacrylic acid and olefin-maleic acid copolymers, particularly ethylene-maleic acid copolymers (hereinafter sometimes abbreviated as “EMA”) have gas barrier properties. From the viewpoint, it is preferably used. EMA is obtained by polymerizing maleic anhydride and ethylene by a known method such as solution radical polymerization. The maleic acid unit in the olefin-maleic acid copolymer tends to have a maleic anhydride structure in which the adjacent carboxyl group is dehydration-cyclized in a dry state, and opens to form a maleic acid structure when wet or in an aqueous solution. Therefore, in the present invention, unless otherwise specified, maleic acid units and maleic anhydride units are collectively referred to as maleic acid units. The maleic acid unit in EMA is preferably 5 mol% or more, more preferably 20 mol% or more, further preferably 30 mol% or more, and most preferably 35 mol% or more. . Moreover, it is preferable that the weight average molecular weights of EMA are 1000-1 million, It is more preferable that it is 3000-500000, It is further more preferable that it is 7000-300000, It is especially preferable that it is 10000-200000.

  In the present invention, the gas barrier layer (II) preferably contains a polyalcohol. By containing the polyalcohol, the polycarboxylic acid in the gas barrier layer (II) reacts with the polyalcohol in addition to reacting with the metal compound in the plastic substrate (I), thereby improving the gas barrier property. be able to. Polyalcohol is a compound having two or more hydroxyl groups in the molecule. Examples of low molecular weight compounds include sugar alcohols such as glycerin and pentaerythritol, monosaccharides such as glucose, disaccharides such as maltose, and oligosaccharides such as galactooligosaccharide. Examples of the polymer compound include polysaccharides such as polyvinyl alcohol, ethylene-vinyl alcohol copolymer, and starch. The said polyalcohol may be used independently and may be used together. The saponification degree of polyvinyl alcohol or ethylene-vinyl alcohol copolymer is preferably 95 mol% or more, and more preferably 98 mol% or more. Moreover, it is preferable that average polymerization degree is 50-2000, and it is more preferable that it is 200-1000.

  The polycarboxylic acid and the polyalcohol in the gas barrier layer (II) are preferably contained so that the molar ratio of OH group to COOH group (OH group / COOH group) is 0.01-20. It is more preferable to contain so that it may become 01-10, It is more preferable to contain so that it may become 0.02-5, It is most preferable to contain so that it may become 0.04-2.

  In the present invention, the gas barrier layer (II) preferably contains polyacrylamide, polymethacrylamide or polyamine. By containing these compounds, the polycarboxylic acid in the gas barrier layer (II) reacts with these compounds in addition to reacting with the metal compound in the plastic substrate (I). Can be improved.

  The polyamine has two or more amino groups selected from primary and secondary as amino groups in the molecule. Specific examples thereof include polyallylamine, polyvinylamine, branched polyethyleneimine. And polysaccharides having an amino group in the side chain such as linear polyethyleneimine, polylysine and chitosan, and polyamides having an amino group in the side chain such as polyarginine. The weight average molecular weight of the polyamine is preferably 5,000 to 150,000. If the weight average molecular weight of the polyamine is too low, the resulting gas barrier layer (II) becomes fragile. On the other hand, if the molecular weight is too high, handling properties are impaired, and in some cases, a gas barrier layer (II) described later is formed. Therefore, the gas barrier layer (II) obtained by agglomeration in the coating liquid may have a gas barrier property impaired.

  The mass ratio of polyamine to polycarboxylic acid (polyamine / polycarboxylic acid) in the gas barrier layer (II) is preferably 12.5 / 87.5 to 27.5 / 72.5. If the mass ratio of the polyamine is lower than this, the crosslinking of the carboxyl group of the polycarboxylic acid becomes insufficient. Conversely, if the mass ratio of the polyamine is higher than this, the crosslinking of the amino group of the polyamine becomes insufficient. However, the gas barrier laminate obtained may be inferior in gas barrier properties.

  The gas barrier layer (II) in the present invention may contain a crosslinking agent. By containing a cross-linking agent, gas barrier properties can be enhanced. The content of the crosslinking agent in the gas barrier layer (II) is preferably 0.1 to 30 parts by mass and more preferably 1 to 20 parts by mass with respect to 100 parts by mass of the polycarboxylic acid.

  Examples of the crosslinking agent include a compound having self-crosslinking property and a compound having a plurality of functional groups that react with a carboxyl group in the molecule. When the gas barrier layer (II) contains a polyalcohol, it reacts with a hydroxyl group. A compound having a plurality of functional groups in the molecule may also be used. Preferable examples of the crosslinking agent include isocyanate compounds, melamine compounds, urea compounds, epoxy compounds, carbodiimide compounds, zirconium salt compounds such as zirconium ammonium carbonate, metal alkoxides, and the like. These crosslinking agents may be used alone or in combination.

  A metal alkoxide is a compound containing a metal to which an alkoxy group is bonded, and an alkyl group substituted with a functional group having reactivity with a halogen or a carboxyl group may be bonded instead of a part of the alkoxy group. . Here, the metal includes atoms such as silica, aluminum, titanium, and zirconium, the halogen includes chlorine, iodine, bromine, and the like. The functional group having reactivity with a carboxyl group is an epoxy group. , Amino group, isocyanate group, ureido group and the like, and alkyl group includes methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, iso-butyl group and the like. Examples of such compounds include tetramethoxysilane, tetraethoxysilane, chlorotriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-aminopropyltrimethoxysilane, Alkoxysilane compounds such as 3-aminopropyltriethoxysilane, 3-ureidopropyltriethoxysilane, 3-isocyanatopropyltriethoxysilane, alkoxytitanium compounds such as tetraisopropoxytitanium and tetraethoxytitanium, alkoxy such as triisopropoxyaluminum Examples include aluminum compounds and alkoxyzirconium compounds such as tetraisopropoxyzirconium.

  These metal alkoxides must be partially or wholly hydrolyzed, partially hydrolyzed or condensed, fully hydrolyzed and partially condensed, or a combination of these. You can also.

  When the above metal alkoxide and polycarboxylic acid are mixed, it may be difficult for both to react and to be applied. Therefore, it is preferable to form a hydrolysis condensate in advance before mixing. As a method for forming the hydrolysis-condensation product, a method used in a known sol-gel method can be applied.

  In the gas barrier layer (II) in the present invention, a reinforcing material, a pigment, a weathering agent, a flame retardant, a plasticizer, a release agent, Lubricants, preservatives, antifoaming agents, wetting agents, viscosity modifiers and the like may be added. Examples of the reinforcing material include clay, talc, wollastonite, silica, alumina, calcium silicate, sodium aluminate, sodium aluminosilicate, magnesium silicate, glass balloon, carbon black, zeolite, montmorillonite, hydrotalcite, fluorine mica, Examples include metal fibers, metal whiskers, ceramic whiskers, potassium titanate whiskers, boron nitride, graphite, glass fibers, carbon fibers, fullerenes (C60, C70, etc.), carbon nanotubes, and the like.

  In the present invention, the thickness of the gas barrier layer (II) laminated on the plastic substrate (I) is preferably thicker than 0.05 μm in order to sufficiently enhance the gas barrier property of the gas barrier laminate, from the economical viewpoint. Therefore, it is preferable that the thickness is less than 5.0 μm.

  The gas barrier layer (II) in the present invention can be formed by applying and drying a gas barrier layer (II) forming coating solution on the plastic substrate (I). Since the coating liquid is preferably aqueous from the viewpoint of workability, the polycarboxylic acid, polyalcohol and polyamine constituting the coating liquid are preferably water-soluble or water-dispersible, and water-soluble. It is more preferable that

  In the present invention, when an aqueous coating solution is prepared by mixing a polycarboxylic acid and a polyalcohol, it is preferable to add 0.1 to 20 equivalent% of an alkali compound with respect to the carboxyl group of the polycarboxylic acid. . Since polycarboxylic acid has high hydrophilicity when the content of carboxyl group is large, it can be made into an aqueous solution without adding an alkali compound. However, the gas barrier property of the obtained gas barrier laminate can be remarkably improved by adding an appropriate amount of an alkali compound. The alkali compound only needs to be capable of neutralizing the carboxyl group of the polycarboxylic acid, and the addition amount thereof is preferably 0.1 to 20 mol% with respect to the carboxyl group of the polycarboxylic acid.

  The coating liquid can be prepared by a known method using a melting pot equipped with a stirrer. For example, a polycarboxylic acid and a polyalcohol are separately made into aqueous solutions and mixed before coating. The method is preferred. At this time, if the alkali compound is added to the aqueous solution of the polycarboxylic acid, the stability of the aqueous solution can be improved.

  Moreover, in this invention, when mixing polycarboxylic acid and polyamine and preparing an aqueous coating liquid, in order to suppress gelatinization, it is preferable to add a base to polycarboxylic acid. The base may be any as long as it does not inhibit the gas barrier properties of the resulting gas barrier laminate, and examples thereof include inorganic substances such as sodium hydroxide and calcium hydroxide, and organic substances such as ammonia, methylamine, diethanolamine, and the like. Ammonia is preferable because it is easily volatilized by heat treatment. The addition amount of the base is preferably 0.6 equivalents or more, more preferably 0.7 equivalents or more, and further preferably 0.8 equivalents or more with respect to the carboxyl group of the polycarboxylic acid. . If the amount of the base added is small, the coating solution may gel during coating, making it difficult to form the gas barrier layer (II) on the plastic substrate (I).

  The method for applying the gas barrier layer (II) forming coating liquid to the plastic substrate (I) is not particularly limited, and an air knife coater, kiss roll coater, metering bar coater, gravure roll coater, reverse roll coater, dip coater. , Die coater, etc., or a combination of these can be used.

  After the coating liquid for forming the gas barrier layer (II) is applied to the plastic substrate (I), heat treatment may be performed immediately to form a dry film and heat treatment at the same time. Heat treatment may be performed after moisture or the like is evaporated by spraying or infrared irradiation to form a dry film. It is preferable to perform the heat treatment immediately after the coating unless there is a particular obstacle to the state of the gas barrier layer (II) and physical properties such as gas barrier properties. It does not specifically limit as a heat processing method, The method of heat-processing in dry atmosphere, such as oven, is mentioned. Considering shortening of the process, it is preferable to stretch the plastic substrate (I) after applying the gas barrier layer (II) forming coating solution. In any of the above cases, it is preferable that the plastic substrate (I) on which the gas barrier layer (II) is formed is subjected to a heat treatment for 5 minutes or less in a heated atmosphere of 100 ° C. or higher.

  When the gas barrier layer (II) contains a polycarboxylic acid and a polyalcohol, it can be affected by their ratio, presence / absence of additive components, content thereof, and the like. The heat treatment temperature cannot be generally specified, but is preferably 100 to 300 ° C, more preferably 120 to 250 ° C, further preferably 140 to 240 ° C, and 160 to 220 ° C. It is particularly preferred. If the heat treatment temperature is too low, the cross-linking reaction between the polycarboxylic acid and the polyalcohol cannot be sufficiently advanced, and it may be difficult to obtain a laminate having sufficient gas barrier properties, while it is too high. In addition, the gas barrier layer (II) and the like may become brittle. The heat treatment time is preferably 5 minutes or less, more preferably from 1 second to 5 minutes, further preferably from 3 seconds to 2 minutes, and particularly preferably from 5 seconds to 1 minute. . If the heat treatment time is too short, the cross-linking reaction cannot proceed sufficiently, and it becomes difficult to obtain a laminate having gas barrier properties. On the other hand, if it is too long, productivity decreases.

  The coating liquid for forming the gas barrier layer (II) applied to the plastic substrate (I) is irradiated with high-energy rays such as ultraviolet rays, X-rays, and electron beams as necessary before and after the drying. May be. In such a case, a component that is crosslinked or polymerized by irradiation with high energy rays may be blended.

Since the laminate of the present invention has the above-described configuration, it has excellent gas barrier properties, and the laminate after retort treatment or hydrothermal treatment was measured under an atmosphere of 20 ° C. and a relative humidity of 65%. The oxygen permeability can be set to 150 mL / (m ² · day · MPa) or less. The oxygen permeability is preferably 100 mL / (m ² · day · MPa) or less, and more preferably 50 mL / (m ² · day · MPa) or less.

  The laminate of the present invention preferably has a tensile strength of 150 MPa or more, and more preferably 180 MPa or more. If the tensile strength is less than 150 MPa, the mechanical strength is not sufficient, and the piercing strength may decrease. From the same viewpoint as the tensile strength, the tensile elongation is preferably 60% or more, and more preferably 80% or more. Moreover, the laminated body of this invention can make 80% or more the tensile strength retention before and behind a retort process. The tensile strength retention is preferably 85% or more, and more preferably 90% or more.

  The pinhole resistance of the laminate of the present invention is preferably 100 or less, more preferably 20 or less, in the 500 times repeated bending fatigue test at 5 ° C. atmosphere. Specifically, the pinhole resistance is Fed. Shown in MIL-B-131F. Test Method Std. In accordance with Method 2017 of 101C, a sample of 12 inches × 8 inches is gripped in a cylindrical shape with a diameter of 3.5 inches, with an initial gripping distance of 7 inches and a gripping distance of 1 inch at maximum bending, a so-called gel bot tester (manufactured by Rigaku Corporation) The number of pinholes generated after being bent 500 times at 5 ° C. was measured and evaluated.

  Regarding the transparency of the laminate of the present invention, the haze is preferably 70% or less, more preferably 50% or less, further preferably 30% or less, and particularly preferably 15% or less. Most preferably, it is 10% or less. However, this is not the case because transparency may not be required depending on the application.

  The gas barrier laminate of the present invention can be produced by the following method.

  The plastic substrate (I) made of a single layer film is made of, for example, a thermoplastic resin in which a metal compound and an antioxidant are mixed, heated and melted with an extruder, and extruded into a film form from a T-die. Then, the film is cooled and solidified on a cooling drum rotating by a known casting method such as an electrostatic application casting method to obtain an unstretched plastic substrate (I) film.

  In the case of the plastic substrate (I) composed of a multilayer film, for example, a thermoplastic resin in which a metal compound and an antioxidant are mixed is heated and melted by the extruder A, and the thermoplastic resin and the antioxidant are used. Is heated and melted with an extruder B, and two types of melted resins are overlapped in a die, for example, a film having a two-layer structure of a metal-containing layer (M) / a metal-free layer (R) is formed from a T die. It can be obtained in an unstretched state by extruding and cooling and solidifying as described above.

  By including the metal compound in the plastic substrate (I) by such a method, the step of laminating the layer containing the metal compound, which has been conventionally performed, on the substrate can be omitted.

  The gas barrier layer (II) forming coating solution is applied to the obtained single-layer or multi-layer unstretched film by the above-described method to form the gas barrier layer (II), and the tenter-type simultaneous biaxial stretching machine is used. By simultaneously performing biaxial stretching in the machine direction (MD) and the transverse direction (TD), a simultaneously biaxially stretched laminate can be obtained.

  Moreover, after extending | stretching the obtained unstretched film to MD, by apply | coating the coating liquid for gas barrier layer (II) formation by the above-mentioned method, gas barrier layer (II) is formed, and then extending | stretching to TD. A plastic substrate (I) that is successively biaxially stretched can be obtained. In addition, when the unstretched film is oriented, the stretchability may be lowered in a later step. Therefore, the unstretched film is preferably substantially amorphous and non-oriented. It is more preferable to transfer it to a water tank whose temperature is adjusted so as not to exceed 80 ° C., to perform water immersion treatment within 5 minutes, and to perform moisture absorption treatment of 0.5 to 15%.

In addition, the stretching ratio of the film is preferably 1.5 times or more in the case of uniaxial stretching, and also in the case of longitudinal and lateral biaxial stretching, it is preferably 1.5 times or more in the vertical and horizontal directions. Usually, it is preferably 3 times or more, more preferably 6 to 20 times, and even more preferably 6.5 to 13 times. When the draw ratio is in this range, a laminate having excellent mechanical properties can be obtained.

  The film that has undergone the stretching process is heat-set at a temperature of 150 to 220 ° C. in the tenter where the stretching process has been performed, and is 0 to 10%, preferably 2 to 6% as necessary. Alternatively, MD relaxation treatment is performed. In order to reduce the heat shrinkage rate, it is desirable not only to optimize the temperature and time of the heat setting time, but also to perform the heat relaxation process at a temperature lower than the maximum temperature of the heat setting process.

  The stretching method is not particularly limited, but it is preferable to use a simultaneous biaxial stretching method. In general, the simultaneous biaxial stretching method can have practical characteristics such as mechanical characteristics, optical characteristics, thermal dimensional stability, and pinhole resistance. In addition, in the sequential biaxial stretching method in which the transverse stretching is performed after the longitudinal stretching, the orientation crystallization of the film proceeds during the longitudinal stretching, and the stretchability of the thermoplastic resin during the transverse stretching is reduced, thereby blending the metal compound. When the amount is large, the breaking frequency of the film tends to increase. For this reason, in this invention, it is preferable to perform a water absorption process and to take the simultaneous biaxial stretching method.

  The laminated body of this invention can also be processed in the humidified atmosphere after manufacturing a laminated body for the purpose of improving gas barrier property. By the humidification treatment, the action of the metal compound of the plastic substrate (I) and the polycarboxylic acid of the gas barrier layer (II) can be further promoted. In such humidification treatment, the laminate may be left in an atmosphere of high temperature and high humidity, or the laminate may be directly contacted with high temperature water. Humidification conditions vary depending on various purposes, but when left in an atmosphere of high temperature and high humidity, a temperature of 30 to 130 ° C. and a relative humidity of 50 to 100% are preferable. Also when making it contact with high temperature water, the temperature of about 30-130 degreeC (100 degreeC or more is under pressure) is preferable. The humidifying treatment time varies depending on the treatment conditions, but generally a range of several seconds to several hundred hours is selected.

  The laminate of the present invention may be subjected to a surface treatment such as a corona discharge treatment as necessary.

  The laminate of the present invention may be laminated with a sealant or the like.

  The resin used as the sealant is low density polyethylene, medium density polyethylene, high density polyethylene, linear low density polyethylene, polypropylene, polyethylene / polypropylene copolymer, ethylene-vinyl acetate copolymer, ionomer resin, ethylene-acrylic acid. / Methacrylic acid copolymer, ethylene-acrylic acid / methacrylic ester copolymer, polyvinyl acetate resin, etc., polyethylene, polypropylene, polyethylene / polypropylene copolymer, etc. with high heat seal strength and material strength The polyolefin resin is preferred. These resins may be used alone, or may be copolymerized or melt-mixed with other resins, or may be further acid-modified.

  As a method for forming a sealant layer in a gas barrier laminate, a film or sheet made of a sealant resin is laminated to the gas barrier laminate via an adhesive, or the sealant resin is extruded and laminated to the gas barrier laminate. And the like. In the former method, the film or sheet made of the sealant resin may be in an unstretched state or in a stretched state at a low magnification, but practically preferably in an unstretched state.

  Although the thickness of a sealant layer is not specifically limited, It is preferable that it is 20-100 micrometers, and it is more preferable that it is 40-70 micrometers.

  A packaging bag can be produced using the laminate of the present invention, and this packaging bag is, for example, a food / beverage product, fruit, juice, drinking water, liquor, cooked food, marine product, frozen food, meat product, Contents such as boiled foods, rice cakes, liquid soups, seasonings, other various foods and beverages, liquid detergents, cosmetics, and chemical products can be filled and packaged.

  EXAMPLES Next, although an Example demonstrates this invention concretely, this invention is not limited to these Examples.

1. Measurement Method (1) Average Particle Size A cumulative percent value of 50% in a particle size distribution (volume distribution) curve measured with a laser particle size analyzer “Microtrac HRA” (manufactured by Nikkiso Co., Ltd.) was determined. A sample for measuring the average particle diameter was prepared by adding 50 g of isopropanol to 0.5 g of the metal compound and performing ultrasonic dispersion treatment for 3 minutes.

(2) Thickness of each layer The laminate was allowed to stand for 2 hours or more in an environment of 23 ° C. and 50% RH, and then the film cross-section was observed with a scanning electron microscope (SEM) to measure the thickness of each layer.

(3) Oxygen permeability After the laminate was hydrothermally treated (treated at 95 ° C. for 30 minutes), it was allowed to stand in an environment of 23 ° C. and 50% RH for 2 hours or more, and an oxygen barrier measuring instrument manufactured by Mocon ( OX-TRAN 2/20) was used to measure oxygen permeability in an atmosphere at a temperature of 20 ° C. and a relative humidity of 65%. The unit is mL / (m ² · day · MPa).
Moreover, after performing the retort process (processed on 130 degreeC x 270 kPa x30 minute conditions) the laminated body different from the sample which carried out the hot water process, the oxygen permeability was measured similarly to the above. In addition, the retort process was performed by the hot water spray system, fixing the laminated body to the aluminum frame, and using the high temperature / high pressure cooking sterilization processing apparatus (RCS-60SPXTG by the Nisaka Manufacturing Co., Ltd.).

(4) Tensile strength retention rate From the laminate subjected to the retort treatment in (3), a strip-shaped test piece having a width of 15 mm is collected in two directions so that the long side is parallel to each of MD and TD. In an atmosphere of 20 ° C. and 65% RH, the tensile strength was measured using a tensile tester (AGS-100B type, manufactured by Shimadzu Corporation) at a grip distance of 100 mm and a tensile speed of 500 mm / min. Tensile strength retention was determined from the measured values before and after the retort treatment.

2. Raw materials The raw materials used in the following examples and comparative examples are as follows.
(1) Thermoplastic resin for plastic substrate PA6: Polyamide 6 resin (A1030BRF, manufactured by Unitika Ltd., relative viscosity 3.0)
PET: Polyethylene terephthalate resin (Unitika, UT-CBR, intrinsic viscosity 0.62)

(2) Metal compound for plastic substrate / MgO: Magnesium oxide (Puremag FNM-G average particle size 0.4 μm, manufactured by Tateho Chemical Co., Ltd.)
MgCO ₃ : Magnesium carbonate (manufactured by Kamishima Chemical Industry Co., Ltd. MSS average particle size 1.2 μm)
-CaCO ₃ : Calcium carbonate (Vigot 15 average particle size 0.5 μm, manufactured by Shiroishi Kogyo Co., Ltd.)
ZnO: Zinc oxide (FINEX-50 average particle size 0.02 μm, manufactured by Sakai Chemical Industry Co., Ltd.)

(3) Antioxidant / antioxidant A for plastic substrates: Irganox 1098 (N, N′-hexamethylenebis (3,5-di-tert-butyl-4-hydroxy-hydrocinnamide), Ciba・ Specialty Chemicals)
Antioxidant B: Irganox 1010 (pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], manufactured by Ciba Specialty Chemicals)

(4) Metal compound master chip A metal compound master chip was prepared by kneading 15 parts by mass of a metal compound and 85 parts by mass of a thermoplastic resin according to Examples and Comparative Examples.
In addition, about the metal compound master chip used for Example 17 and the comparative example 2, it was set as the compounding ratio of 75 mass parts of magnesium oxide and 25 mass parts of polyamide 6 resin.

(4) Polycarboxylic acid component / EMA aqueous solution of gas barrier layer forming coating solution:
EMA (weight average molecular weight 60000) and sodium hydroxide were added to water, dissolved by heating and then cooled to room temperature. 10 mol% of the carboxyl group of EMA was neutralized with sodium hydroxide, solid content 15 Mass% EMA aqueous solution.
-PAA aqueous solution:
10 mol% of the carboxyl group of polyacrylic acid prepared with polyacrylic acid (A10H, manufactured by Toagosei Co., Ltd., number average molecular weight 200000, 25 wt% aqueous solution) and sodium hydroxide was neutralized with sodium hydroxide. An aqueous polyacrylic acid (PAA) solution having a solid content of 15% by mass.

(5) Other resin components and PVA aqueous solution for gas barrier layer forming coating solution:
Polyvinyl alcohol (Polyal 105 manufactured by Kuraray Co., Ltd., saponification degree 98 to 99%, average polymerization degree about 500) was added to water, dissolved by heating, and then cooled to room temperature. PVA) aqueous solution.
・ PAM:
Polyacrylamide (manufactured by Kishida Chemical Co., Ltd., reagent, weight average molecular weight 9 million to 10 million, polymerization degree 1270 to 141,000).

Example 1
The polyamide 6 resin, the metal compound master chip, and the antioxidant A were mixed so that the magnesium oxide content was 0.1 mass% and the antioxidant A content was 0.06 mass%. This mixture was charged into an extruder and melted in a 270 ° C. cylinder. The melt was extruded into a sheet form from a T-die orifice, was brought into close contact with a rotating drum cooled to 10 ° C., and rapidly cooled to obtain an unstretched polyamide film having a thickness of 150 μm. The obtained unstretched film was sent to a 50 ° C. hot water tank and subjected to a water immersion treatment for 2 minutes.
Next, an EMA aqueous solution and a PVA aqueous solution were mixed so that the mass ratio (solid content) of PVA and EMA was 5/5 to obtain a gas barrier layer forming coating solution having a solid content of 10% by mass. . This coating solution was applied to one side of an unstretched film that had been subjected to water immersion treatment, and then dried.
The end of the film was held by a clip of a tenter simultaneous biaxial stretching machine, and stretched at 180 ° C. to MD and TD by 3.3 times. Thereafter, a heat treatment was performed at 210 ° C. for 4 seconds at a relaxation rate of TD of 5%, and gradually cooled to room temperature to laminate a polyamide film having a thickness of 15 μm and a gas barrier layer having a thickness of 0.3 μm. Obtained.

Examples 2-11, 13-16, Comparative Examples 1, 3, 4
In the same manner as in Example 1 except that the thermoplastic compound, the metal compound master chip, and the antioxidant were mixed so that the content of the metal compound and antioxidant shown in Table 1 were as shown in Table 1, A stretched film was obtained and immersed in water.
Next, for other resins such as PVA and polycarboxylic acids, the gas barrier layer formation was performed in the same manner as in Example 1 except that the types and mass ratios (solid contents) were as shown in Table 1. A coating solution was prepared.
Using the obtained coating solution, in the same manner as in Example 1, after applying to an unstretched film, drying, and then biaxially stretching, a gas barrier laminate was obtained.
In Example 16, the polyethylene terephthalate resin (PET) was used as the thermoplastic resin, and the conditions were changed as follows. That is, an unstretched film was produced at a cylinder temperature of 280 ° C., and the obtained unstretched film was not subjected to water immersion treatment. Moreover, the temperature in simultaneous biaxial stretching was 90 degreeC, and the temperature of heat processing was 230 degreeC.

Example 12
A coating solution for forming the gas barrier layer (II) was prepared as follows.
That is, polyacrylic acid (PAA) having a number average molecular weight of 200,000 was dissolved in distilled water to obtain a PAA aqueous solution having a solid content concentration of 13% by mass in the aqueous solution. Subsequently, a 13% by mass aqueous ammonia solution was added to the aqueous PAA solution to neutralize 1 mol% of the carboxyl groups of the PAA, thereby obtaining a partially neutralized aqueous solution of PAA.
Further, 100 parts by mass of polyacrylic acid (PAA) having a number average molecular weight of 40,000 was dissolved in 1064 parts by mass of methanol, and then 166 parts by mass of γ-aminopropyltrimethoxysilane (APTMOS) was added with stirring. Thus, an APTMOS methanol solution (12-1) was obtained. In the APTMOS methanol solution (12-1), at least a part of the amino group of APTMOS is neutralized by the carboxyl group of PAA.
Next, a TMOS methanol solution was prepared by dissolving 34.5 parts by mass of tetramethoxysilane (TMOS) in 34.5 parts by mass of methanol. While maintaining the temperature of this TMOS methanol solution at 10 ° C. or lower, 2.3 parts by weight of distilled water and 5.7 parts by weight of 0.1M hydrochloric acid were added, and hydrolysis and condensation were carried out at 10 ° C. for 60 minutes with stirring. By performing the reaction, a solution (12-2) was obtained.
Subsequently, the solution (12-2) was diluted with 214.7 parts by mass of methanol and 436.1 parts by mass of distilled water, and then 235.9 parts by mass of the partially neutralized aqueous solution of PAA was added with stirring. A solution (12-3) was obtained.
Subsequently, 36.2 parts by mass of the APTMOS methanol solution (12-1) was added while stirring the solution (12-3), and the mixture was further stirred for 30 minutes to obtain a solution (12-4).
A laminate was obtained in the same manner as in Example 1 except that the solution (12-4) prepared by the above method was used as a gas barrier layer-forming coating solution.

Example 17
Polyamide 6 resin, metal compound master chip and antioxidant A were mixed and mixed so that the content of magnesium oxide was 50 parts by mass and the content of antioxidant A was 0.06% by mass. This mixture was put into an extruder A and melt-extruded at 260 ° C. On the other hand, a raw material obtained by mixing 0.06% by mass of antioxidant A with polyamide 6 resin was put into an extruder B and melt-extruded at 260 ° C.
Two types of resins melted in the extruder A and the extruder B are overlapped in a die, and a sheet having a two-layer structure of a metal-containing layer (M) / resin layer (R) is extruded from a T die, and a surface temperature of 20 An unstretched multi-layer polyamide film having a thickness of 150 μm, which is (M) / (R) = 5/145 μm, was obtained by closely adhering to a cooling roll at 0 ° C. The obtained unstretched multilayer film was sent to a 50 ° C. hot water tank and subjected to water immersion treatment for 2 minutes.
Next, the coating liquid prepared in the same manner as in Example 1 was applied to the metal-containing layer (M) surface of the unstretched multilayer film and then dried.
In the same manner as in Example 1, it was subjected to simultaneous biaxial stretching and heat treatment, and consisted of a metal-containing layer (M) having a thickness of 0.5 μm and a resin layer (R) having a thickness of 14.5 μm, having a thickness of 15 μm. A laminate in which a gas barrier layer having a thickness of 0.3 μm was laminated on the metal-containing layer (M) of the laminate was obtained.

Examples 18, 19, 21
Extruder A is mixed so that the polyamide 6 resin, the metal compound master chip and the antioxidant A are mixed so as to have the composition shown in Table 1, and the thickness after stretching is the thickness structure shown in Table 1. A non-stretched multilayer film was obtained in the same manner as in Example 17 except that the extrusion amount of B was changed, and was subjected to water immersion treatment.
Next, for other resins such as PVA and polycarboxylic acids, coating for gas barrier layer formation was performed in the same manner as in Example 1 except that the mass ratio (solid content) was as shown in Table 1. A liquid was prepared.
Using the obtained coating solution, after applying to the metal-containing layer (M) surface of the unstretched film and drying, as in Example 17, except that the thickness after stretching is the thickness described in Table 1. Simultaneously biaxially stretching to obtain a laminate.

Example 20
Extruder A was applied so that the gas barrier layer (II) -forming coating solution was applied to the resin layer (R) surface of the unstretched multilayer film, and the thickness after stretching was as shown in Table 1. Resin layer (R) of 15 μm polyamide film comprising a metal-containing layer (M) having a thickness of 3 μm and a resin layer (R) having a thickness of 12 μm, in the same manner as in Example 17 except that the extrusion amount of B was changed. ) Was laminated with a gas barrier layer having a thickness of 0.3 μm.

Comparative Example 2
An unstretched polyamide film was obtained and subjected to water immersion treatment in the same manner as in Example 1 except that the metal compound master chip was changed so that the content of the metal compound was 75% by mass.
Next, for other resins such as PVA and polycarboxylic acids, the gas barrier layer formation was performed in the same manner as in Example 1 except that the types and mass ratios (solid contents) were as shown in Table 1. A coating solution was prepared.
Using the obtained coating solution, it was attempted to simultaneously biaxially stretch after coating and drying on an unstretched film in the same manner as in Example 1, but the film was broken during stretching to obtain a gas barrier laminate. I couldn't.

  Table 1 shows the configurations of the laminates obtained in Examples and Comparative Examples and the evaluation results thereof.

As for the laminated body of Examples 1-21, as for all, the tensile strength retention before and behind retort processing is 80% or more, and the oxygen permeability after retort processing is 150 mL / (m < ² > * day) after boil processing.・ MPa) or less.

In the laminate of Comparative Example 1, since the metal compound contained in the laminate was less than 0.1% by mass, the oxygen permeability after the retort treatment exceeded 150 mL / (m ² · day · MPa). .
Since the laminate of Comparative Example 3 did not contain a polycarboxylic acid in the gas barrier layer (II), the oxygen permeability after the retort treatment exceeded 150 mL / (m ² · day · MPa).
The laminate of Comparative Example 4 had a tensile strength retention before and after the retort treatment of less than 80%.

Claims (8)

The plastic substrate (I) will be the gas barrier layer (II) is laminated, comprising a plastic substrate (I) is a metal compound and 0.1 to 70 wt% of an antioxidant 0.03 wt% Including a metal-containing layer
The gas barrier layer (II) contains a polycarboxylic acid ,
The metal-containing layer is obtained by extruding a melt of a thermoplastic resin in which a metal compound and an antioxidant are mixed.
The metal-containing layer and the layer (II) containing polycarboxylic acid are in contact;
After retorting at 130 ° C. for 30 minutes, the oxygen permeability under an atmosphere of 20 ° C. and 65% relative humidity is 150 mL / (m ² · day · MPa) or less.
The tensile strength retention before and after retorting at 130 ° C. for 30 minutes is 85% or more,
The plastic substrate (I) is stretched,
A laminate characterized by the above. The laminate according to claim 1, wherein the antioxidant is a hindered phenol-based antioxidant. The hindered phenolic antioxidant is pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] or N, N′-hexamethylenebis (3,5 The laminate according to claim 2, which is -di-t-butyl-4-hydroxy-hydrocinnamide). The laminate according to any one of claims 1 to 3, wherein the plastic substrate (I) is a multilayer film. The laminate according to any one of claims 1 to 4, wherein the gas barrier layer (II) contains a polyalcohol. The metal which comprises a metal compound is 1 type chosen from magnesium, calcium, and zinc, The laminated body in any one of Claims 1-5 characterized by the above-mentioned. After the hydrothermal treatment at 95 ° C. for 30 minutes, the oxygen permeability in an atmosphere at 20 ° C. and 65% relative humidity is 150 mL / (m ² (Day * MPa) or less, The laminated body in any one of Claims 1-6 characterized by the above-mentioned. A packaging bag comprising the laminate according to any one of claims 1 to 7 .