JP5566238B2 - Laminated body and method for producing the same - Google Patents

Description

  The present invention relates to a laminate used for a packaging material. In particular, the present invention relates to a laminate in which polypropylene is used as a sealant resin.

  Many packaging materials have a laminated structure in which a plurality of layers are laminated. For example, a packaging material having a structure in which a polyolefin resin film is laminated as a sealant layer on an upper surface of a barrier layer such as an aluminum foil via an adhesive layer (also called a primer or an anchor coat layer) is often used. As the sealant resin, polyethylene or polypropylene is used. Among these, polypropylene is used as a sealant resin for food packaging materials that require heat sterilization treatment such as boiling and retort because of its excellent heat resistance and oil resistance.

  As a method for producing a laminate having such a structure, a dry laminate method in which a base material having a barrier layer is coated, an adhesive layer is provided by drying, and then the film is preliminarily bonded to a sealant resin film and heated with a heating roll. Alternatively, there is an extrusion laminating method in which a base material having a barrier layer is coated and dried to provide an adhesive layer, and then a molten sealant resin is extruded from an extruder to form a sealant layer. The extrusion laminating method forms a sealant layer by directly melt-extruding a sealant resin on a substrate provided with an adhesive layer, so that the process of forming a sealant resin film can be omitted, and it is simple and low cost. Suitable for mass production in Japan.

  As an excellent adhesive layer in the case of producing a laminate by an extrusion laminating method, Patent Document 1 proposes an adhesive layer containing an acid-modified polyolefin and a polyurethane resin, and when polyethylene is used as a sealant resin, A packaging material in which the layer and the barrier layer are firmly bonded is obtained. However, in this invention, the evaluation of the adhesive layer when polypropylene is used as the sealant resin has not been made. Actually, when the sealant resin was polypropylene, the adhesive layer did not have sufficient adhesive force. .

  Further, Patent Document 2 proposes a method for improving the adhesive force by performing ozone treatment under specific conditions without using an anchor coating agent. However, this method is complicated not only in special equipment such as ozone treatment but also in equipment and processes, such as requiring aging at a high temperature after lamination. Moreover, the sealant resin used is limited to polyethylene, and polypropylene has not been evaluated.

  Patent Document 3 proposes an adhesive layer containing acid-modified polyolefin. However, when the sealant resin is polypropylene, in order to obtain a packaging material having sufficient adhesion with the barrier layer, the temperature of the extrusion laminate must be set high, in which case the polypropylene is thermally decomposed, Thermal decomposition products may remain in the sealant layer. In some cases, the pyrolyzate may adhere to the contents.

  Thus, it was substantially difficult to produce a laminate by extrusion lamination using polypropylene as a sealant resin.

JP 2008-229971 A Japanese Patent No. 2905328 JP 2008-230198 A

  The present invention provides a laminate in which a sealant layer and a barrier layer have sufficient adhesive force even when polypropylene is used as a sealant resin, even if this is laminated by extrusion lamination to form a sealant layer. Is to provide.

  As a result of intensive studies to solve the above problems, the present inventors have found that the above problems can be solved by using a resin layer containing an acid-modified olefin elastomer as an adhesive layer, and have reached the present invention.

That is, the gist of the present invention is as follows.
(1) A barrier layer, an adhesive layer, and a sealant layer are laminated in this order. The adhesive layer contains an acid-modified olefin elastomer, and the olefin elastomer constituting the acid-modified olefin elastomer is an ethylene / α-olefin copolymer. polymer elastomer, containing at least one of propylene · alpha-olefin copolymer elastomer, the amount of the adhesive layer is a laminate and wherein the scope der Rukoto of 0.001 to 5 g / m ^2.
(2 ) The laminate according to (1 ), wherein the barrier layer contains aluminum.
( 3 ) The laminate according to (1) or (2) , wherein the sealant layer contains a polyolefin resin.
(4) The laminate according to, characterized in that the polyolefin resin is polypropylene (3).
(5) When producing the laminate according to any one of (1) to (4) above, on the barrier layer on which the adhesive layer containing the acid-modified olefin elastomer is formed, the adhesive layer is interposed therebetween. A method for producing a laminate comprising laminating a melted sealant resin by extrusion lamination.
( 6 ) When producing the laminate according to any one of (1) to ( 4 ) above, an adhesive layer containing an acid-modified olefin elastomer is formed on the barrier layer, and then the adhesive layer is interposed therebetween. And a laminated sealant resin is laminated by extrusion lamination.

  By using the adhesive layer constituting the laminate of the present invention, a laminate in which the sealant layer and the barrier layer have an excellent adhesive force even when the sealant layer is laminated by extrusion lamination using polypropylene. Can be manufactured.

  The laminate of the present invention is a laminate in which a barrier layer, an adhesive layer, and a sealant are laminated in this order.

  Examples of the barrier layer constituting the laminate include soft metal foils such as aluminum foil, and vapor deposition layers such as aluminum vapor deposition, silica vapor deposition, alumina vapor deposition, and silica alumina binary vapor deposition. Also, vinylidene chloride resins, modified polyvinyl Examples include an organic barrier layer made of alcohol, ethylene vinyl alcohol copolymer, MXD nylon or the like. These barrier layers are usually used with a base material such as a thermoplastic resin film described later.

  When using a vapor deposition layer as a barrier layer, it is easy to use a commercially available vapor deposition film. As a film having such a vapor deposition layer, for example, “IB series” manufactured by Dai Nippon Printing Co., Ltd., letterpress printing "GL, GX series" manufactured by the company, "Barrier Rocks" manufactured by Toray Film Processing Co., Ltd., VM-PET, YM-CPP, VM-OPP, "Tech Barrier" manufactured by Mitsubishi Plastics, "Metaline" manufactured by Toh Cello, Examples include “MOS”, “Tetrait”, “Bebright” manufactured by Oike Kogyo Co., “Metalite”, “Chemilite” manufactured by Nakai Kogyo Co., Ltd. A protective coating layer may be provided on the vapor deposition layer.

  When an organic barrier layer is used as a barrier layer, there are a method of coating a base film with a coating containing a resin having a barrier property, a method of laminating the resin by a co-extrusion method, and the like. A method using a film having a barrier layer is simple. As a film having such an organic barrier layer, Kuraray's `` Clarista '', `` Eval '', Kureha Chemical Industry's `` Besera '', Mitsubishi Plastics' `` Super Neil '', Kojin's `` "Co-barrier", Unitika's "Savix", "Embron M", "Embron E", "Emblem DC", "Embret DC", "NV", Tosero's "K-OP", "A-OP" "Senesi" manufactured by Daicel Corporation.

The barrier property of the barrier layer can be appropriately selected depending on the use such as the contents to be packaged and the storage period, but generally, the water vapor permeability is preferably 100 g / m ² · day (40 ° C., 90% RH) or less, 20 g / m ² · day or less is more preferable, 10 g / m ² · day or less is more preferable, and 1 g / m ² · day or less is particularly preferable. The oxygen permeability is preferably 100 ml / m ² · day · MPa (20 ° C., 90% RH) or less, more preferably 20 ml / m ² · day · MPa or less, and even more preferably 10 ml / m ² · day · MPa or less. It is preferably 1 ml / m ² · day · MPa or less.

  As the barrier layer, an aluminum foil, a vapor deposition layer such as aluminum, silica, and alumina is preferable from the viewpoint of barrier properties, and an aluminum foil is more preferable from the viewpoint of being inexpensive. Although the thickness of aluminum foil is not specifically limited, The range of 3-50 micrometers is preferable from an economical surface.

The adhesive layer constituting the laminate of the present invention contains an acid-modified olefin elastomer.
The olefin elastomer which is the main component of the olefin elastomer having an acid component in the acid-modified olefin elastomer is a soft segment comprising at least one olefin elastomer polymer part in the molecule and at least one olefin elastomer polymer part. A block copolymer having a hard segment.
Examples of the soft segment comprising the olefin elastomer polymer part include α-olefin random polymer parts such as ethylene, propylene and 1-butene, polymer parts of diene compounds (diolefins) such as butadiene and isoprene, or hydrogen thereof. There are additives, the hard segment is usually a polymer part having an α-olefin polymer part such as ethylene, propylene, 1-butene and the like, a polymer part having a glass transition point such as a polystyrene polymer part at room temperature or higher, Some of the hydrogenated products of the butadiene copolymer have crystallinity.
Examples of the block copolymer component include ethylene-propylene copolymer, ethylene-1-butene copolymer, propylene-1-butene copolymer, and ethylene-propylene-1-butene copolymer. Ethylene, propylene, 1-butene, 3-methyl-1-butene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-butene, 3-methyl-1-pentene, 1-heptene, 1- Examples thereof include olefin elastomers that are α-olefins such as hexene, 1-octene, 1-decene, and 1-dodecene, or copolymers of two or more. In addition, alicyclic structure-containing polymers such as norbornene copolymers, monocyclic cyclic polyolefin polymers, cyclic conjugated diene copolymers, vinyl alicyclic hydrocarbon polymers, and hydrogenated products thereof are also used. be able to.

  Among these, an ethylene-butene copolymer, an ethylene-propylene copolymer, an ethylene-octene copolymer, an ethylene-propylene-butene copolymer, a propylene-butene copolymer, and a propylene-octene copolymer are preferable. An ethylene-butene copolymer, an ethylene-propylene copolymer, and a propylene-butene copolymer are more preferable.

Moreover, the elastomer used for the adhesive layer of the present invention has an acid-modified component. Examples of the acid-modifying component include an unsaturated carboxylic acid component.
Specific examples of the unsaturated carboxylic acid component include acrylic acid, methacrylic acid, maleic acid, maleic anhydride, itaconic acid, itaconic anhydride, fumaric acid, crotonic acid and the like, as well as unsaturated dicarboxylic acid half esters and half amides. Etc. Among these, acrylic acid, methacrylic acid, maleic acid, and maleic anhydride are preferable, and acrylic acid, methacrylic acid, and maleic anhydride are particularly preferable. Two or more of these acid components may be contained in the polyolefin resin.
The unsaturated carboxylic acid component only needs to be copolymerized in the acid-modified polyolefin resin, and the form thereof is not limited. Examples of the copolymerization state include random copolymerization, block copolymerization, and graft copolymerization. (Graft modification) and the like.

  The amount of the acid component contained in the acid-modified olefin elastomer can be determined by measuring the acid value of the resin. The acid value in the present invention is the amount of potassium hydroxide (hereinafter sometimes abbreviated as KOH) required to neutralize 1 g of the acid-modified olefin elastomer resin, and is described in JIS K0070. It can be determined according to the method. In the present invention, the acid value of the acid-modified olefin elastomer is preferably 1 to 500 mgKOH / g, more preferably 3 to 200 mgKOH / g, from the viewpoint of sufficient adhesiveness with the barrier layer or the sealant layer. More preferably, it is 5-100 mgKOH / g, and it is especially preferable that it is 10-50 mgKOH / g. When not acid-modified, there is a high possibility that the adhesion with the barrier layer will be insufficient. Moreover, when an acid value is too large, adhesiveness with a sealant layer may fall.

  Commercially available acid-modified olefin elastomers that can be used in the present invention include Tuffmer series, which are acid-modified olefin elastomers manufactured by Mitsui Chemicals, and Tuftec series manufactured by Asahi Kasei. Specific product names include “MP0610”, “MP0620”, “MH5020”, “MH7020”, “MH7007”, “MH7010”, “MA8510” of the Toughmer series, “M1911”, “M1913” of the Tuftec series. , “M1943” and the like.

The amount of the adhesive layer in the present invention, the area of the bonding surface, is preferably in the range of 0.001 to 5 g / ^{m 2,} more preferably from 0.01~3g / ^{m 2,} 0. further preferably 02~2g / ^{m 2,} particularly preferably from 0.03~1g / ^{m 2,} and most preferably 0.05 to 1 g / ^{m 2.} If it is less than 0.001 g / m ² , sufficient adhesion may not be obtained, and if it exceeds 5 g / m ² , it is economically disadvantageous.

The adhesive layer may contain a small amount of components other than the acid-modified olefin elastomer. For example, polyolefin resin, polyester resin, polyurethane resin, acrylic resin, polyvinyl acetate, ethylene-vinyl acetate copolymer, polyvinyl chloride, polyvinylidene chloride, ethylene-vinyl acetate copolymer, styrene-maleic acid resin, styrene- Butadiene resin, butadiene resin, acrylonitrile-butadiene resin, poly (meth) acrylonitrile resin, (meth) acrylamide resin, chlorinated polyethylene resin, chlorinated polypropylene resin, polyester resin, modified nylon resin, phenol resin, silicone resin, epoxy resin, etc. The resin component is mentioned.
Components other than these acid-modified olefin elastomers are preferably in a range that does not impair the effect of the adhesive layer, and the amount thereof is preferably 20% by mass or less, and preferably 10% by mass or less of the entire adhesive layer. More preferably, it is 5 mass% or less. By adding the resin component, an improvement in adhesion with the barrier layer can be expected.

  Further, the adhesive layer may contain a crosslinking agent for the purpose of improving the adhesion with the barrier layer and improving the heat resistance of the adhesive layer. As the cross-linking agent, it is desirable to use an acid component possessed by the acid-modified olefin elastomer, for example, one having reactivity with a carboxylic acid component. For example, a phenol resin, an amino resin, a polyfunctional epoxy resin, a polyfunctional isocyanate compound and its compound Various block isocyanate compounds, polyfunctional aziridine compounds, carbodiimide group-containing compounds, oxazoline group-containing compounds and the like can be mentioned. Such crosslinking agents may be used alone or in combination of two or more. By improving the heat resistance of the adhesive using a crosslinking agent, the packaging material using the laminate of the present invention has an effect that the adhesiveness is not easily deteriorated even when sterilization treatment such as boiling and retort is performed. Can be expected.

In the present invention, the method for providing the adhesive layer is not particularly limited. For example, an acid-modified olefin elastomer dissolved in an organic solvent or dispersed in an aqueous medium is used as an adhesive, and this is applied to the barrier layer and dried. A method of transferring an adhesive layer obtained by applying an adhesive in which an acid-modified olefin elastomer is dissolved in an organic solvent or dispersed in an aqueous medium on a release paper and then drying the medium onto the barrier layer; an acid-modified olefin elastomer by a T-die Can be melt-extruded onto the barrier layer.
Above all, from the viewpoint that the thickness of the adhesive layer is thin and easy to control uniformly, an acid-modified olefin elastomer dissolved in an organic solvent or dispersed in an aqueous medium is used as an adhesive, and this is applied to the barrier layer and the medium is dried. The method is preferred. When this method is used, an adhesive is applied to the barrier layer, dried to form an adhesive layer, and then the sealant resin is melt-extruded in-line and then cooled and solidified to laminate the sealant layer (extrusion). Laminating method) is simple and particularly preferable.

The medium used to make the above-mentioned acid-modified olefin elastomer dissolved or dispersed in an aqueous medium may be an organic solvent, water, or a mixture of water and a hydrophilic solvent. Also good.
Examples of organic solvents include diethyl ketone (3-pentanone), methyl propyl ketone (2-pentanone), methyl isobutyl ketone (4-methyl-2-pentanone), 2-hexanone, 5-methyl-2-hexanone, and 2-to. Ketones such as butanone, 3-heptanone, 4-heptanone, cyclopentanone, cyclohexanone, aromatic hydrocarbons such as toluene, xylene, benzene, Solvesso 100, Solvesso 150, butane, pentane, hexane, cyclohexane, heptane Aliphatic hydrocarbons such as octane and nonane, methylene chloride, chloroform, carbon tetrachloride, 1,2-dichloroethane, 1,1,2,2-tetrachloroethane, chlorobenzene, o-dichlorobenzene, m-dichlorobenzene, Halogen-containing compounds such as p-dichlorobenzene, acetic acid Esters such as chill, isopropyl acetate, n-butyl acetate, isobutyl acetate, sec-butyl acetate, 3-methoxybutyl acetate, methyl propionate, ethyl propionate, diethyl carbonate, γ-butyrolactone, isophorone, etc. Examples include hydrophilic organic solvents described below.

  Specific examples of the hydrophilic organic solvent include methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol, tert-butanol, n-amyl alcohol, isoamyl alcohol, sec-amyl alcohol, tert. -Amyl alcohol, 1-ethyl-1-propanol, 2-methyl-1-butanol, n-hexanol, cyclohexanol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, etc. Alcohols, ethers such as tetrahydrofuran and 1,4-dioxane, ketones such as acetone and methyl ethyl ketone, methyl acetate, acetic acid-n-propyl, ethyl acetate Esters such as propyl, acetic acid-tert-butyl, methyl propionate, ethyl propionate, dimethyl carbonate, dimethylformamide, dimethylacetamide, diacetone alcohol, acetonitrile, other ammonia, diethylamine, triethylamine, diethanolamine, triethanolamine And organic amine compounds such as N, N-dimethylethanolamine, N, N-diethylethanolamine, N-diethanolamine, 3-methoxypropylamine, 3-diethylaminopropylamine, and dimethylaminopropylamine.

  A method for preparing an adhesive in which the acid-modified olefin elastomer is dissolved or dispersed in an aqueous medium is not particularly limited. For example, the raw material, such as an acid-modified olefin elastomer and an organic solvent, is charged into a sealable container, and the dissolution is performed by stirring while keeping the temperature in the tank at about 40 to 150 ° C. Moreover, as a method of making an acid-modified olefin elastomer into an aqueous dispersion, for example, a method described in International Publication No. 02/055598 pamphlet can be mentioned.

  As a method of applying the adhesive prepared by the above method to the barrier layer, known methods such as gravure roll coating, reverse roll coating, wire bar coating, lip coating, air knife coating, curtain flow coating, spray coating , Dip coating, brush coating, and the like. By applying the adhesive uniformly on the surface of the substrate by such a method, setting it at around room temperature as necessary, and then subjecting it to a drying treatment or a heat treatment for drying, a uniform resin layer is formed on the substrate. It can be formed in close contact with.

A conventionally known sealant resin can be used for the sealant layer of the laminate of the present invention. Examples of the sealant resin include low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), high-density polyethylene (HDPE), acid-modified polyethylene, polypropylene, acid-modified polypropylene, copolymerized polypropylene, and ethylene-vinyl acetate. Examples thereof include polyolefin resins such as polymers, ethylene- (meth) acrylic acid ester copolymers, ethylene- (meth) acrylic acid copolymers, and ionomers.
Especially, since it is cheap, excellent in heat resistance and oil resistance, and applicable to heat sterilization processes, such as a boil and a retort, it is preferable that it is a thing containing a polypropylene, a copolymer polypropylene, or these.
The sealant resin such as polypropylene may contain a polyethylene resin or an olefin elastomer for the purpose of improving the low temperature heat sealability.

Polypropylene is thus a sealant resin with excellent performance. However, as described above, when a resin such as acid-modified polyolefin is used for the adhesive layer, when extrusion laminating polypropylene as a sealant resin, the temperature of the extrusion laminate must be increased from the viewpoint of improving adhesion, At that time, the polypropylene was thermally decomposed, and the thermally decomposed product sometimes remained in the sealant layer. In contrast, in the present invention, since an acid-modified olefin elastomer is used for the adhesive layer, a sealant layer can be formed with good adhesion even when polypropylene is extrusion laminated at a low temperature. It can be significantly suppressed.
Specifically, in the extrusion laminating method, the melt extrusion temperature is generally set to about 270 to 300 ° C. when the sealant resin is melt-extruded from the T die for forming the sealant layer. This is because the sealant layer tends to be formed with good adhesion on the barrier layer as the melt extrusion temperature increases. However, depending on the sealant resin, when the melt extrusion temperature is 270 to 300 ° C., a sealant layer can be formed with good adhesion, while part of the resin component is thermally decomposed, and the thermal decomposition product remains in the sealant layer. Sometimes. Residue of pyrolyzate is not preferable from a hygienic viewpoint. This tendency is particularly remarkable in polypropylene.
In contrast, in the present invention, polypropylene can be extruded and laminated at a low temperature, and a polypropylene sealant layer with good adhesion can be formed while suppressing thermal decomposition of polypropylene. In this case, the melt extrusion temperature of the sealant resin is preferably 230 to 270 ° C, more preferably 230 to 250 ° C.

  In the present invention, when laminating the sealant layer through the adhesive layer as described above, the extrusion laminating method is preferably employed. However, if the sealant layer can be laminated with good adhesion by a method other than the extrusion laminating method, such a method is used. Various methods may be adopted. As a method other than the extrusion laminating method, for example, a method of laminating the adhesive layer and the sealant resin film by heat (dry laminating method) can be employed.

  When the laminate of the present invention is used as a packaging material, the barrier layer is usually used as the outside and the sealant layer is used as the inside (content side), but the rigidity required for the use of the packaging material or the packaging material. In consideration of durability and durability, other layers can be laminated as necessary. Usually, it is used with a base material such as a thermoplastic resin film, synthetic paper or paper on the outside or inside of the barrier layer. In particular, in the step of laminating the barrier layer, the adhesive layer and the sealant layer, the barrier layer is generally used for the step as a laminate with the substrate.

Examples of the thermoplastic resin film include polyester resin films such as polyethylene terephthalate (PET), polyethylene naphthalate (PEN), and polylactic acid (PLA), polyolefin resin films such as polypropylene, polystyrene resin films, 6-nylon, poly- Polyamide resin films such as p-xylylene adipamide (MXD6 nylon), polycarbonate resin films, polyacrylonitrile resin films, polyimide resin films, and multilayers thereof (for example, nylon 6 / MXD / nylon 6, nylon 6 / An ethylene-vinyl alcohol copolymer / nylon 6) or a mixture is used, and those having mechanical strength and dimensional stability are preferable. Of these, a film arbitrarily stretched in the biaxial direction is preferably used.
The thermoplastic resin film may contain a known additive or stabilizer, for example, an antistatic agent, a plasticizer, a lubricant, an antioxidant, or the like, and improves adhesion when laminated with other materials. Therefore, the surface of the film may be subjected to corona treatment, plasma treatment, ozone treatment, chemical treatment, solvent treatment, etc. as pretreatment.
These films may be provided with various coatings such as an easy adhesion coating and an antistatic coating.
The thickness of the thermoplastic resin film is not particularly limited, but considering the suitability as a packaging material and the processability when laminated with other layers, it is practically in the range of 3 to 300 μm, depending on the application, 5 to 30 μm. More preferred.

  In addition, a layer such as a polyamide film or a polyolefin film is laminated between the base material layer and the barrier layer or between the barrier layer and the sealant layer for the purpose of further improving characteristics such as impact resistance and pinhole resistance. For the purpose of improving easy tearability and handcutability, a film having easy tearability and handcutability may be laminated.

  The method for laminating the barrier layer and the thermoplastic resin film, synthetic paper, paper, etc. is not particularly limited. For example, a known two-component mixed adhesive in which a main component having a hydroxyl group or a carboxyl group and an isocyanate compound are mixed. The adhesive can be used. When providing a vapor deposition layer in various base materials, it can carry out by a well-known method. Moreover, when providing an organic barrier layer in a base material, it can carry out by a well-known method.

  There are various forms when making the laminate of the present invention as a packaging material, such as a three-side seal bag, a four-side seal bag, a gusset packaging bag, a pillow packaging bag, and a polypropylene resin chuck is provided on the innermost sealant layer, It can also be a packaging bag with a chuck.

  EXAMPLES Hereinafter, the present invention will be specifically described with reference to examples, but the present invention is not limited thereto.

(1) Acid value of resin 0.15 g of resin was dissolved in 20 ml of tetrahydrofuran, titrated with KOH aqueous solution using cresol red as an indicator, and the acid value (mg KOH / mg) of resin was calculated from the number of mg of KOH consumed for neutralization. g) was determined.

(2) Adhesive layer amount (coating amount)
A liquid material containing an acid-modified olefin elastomer was applied to a substrate whose area and mass were measured in advance, and dried at 100 ° C. for 1 minute. The mass of the obtained laminate was measured, and the coating amount was determined by subtracting the mass of the base material before coating. The layer amount per unit area (g / m ² ) was calculated from the coating amount and the coating area.

(3) Laminate strength A test piece having a width of 15 mm was taken from the laminate film, and a barrier layer and a sealant layer were formed from the end of the test piece by T-type peeling using a tensile tester (precision universal material tester 2020, manufactured by Intesco). The interface was peeled and the strength was measured. The measurement was performed in an atmosphere of 20 ° C. and 65% RH at a tensile speed of 200 mm / min. A laminate strength of 2 N / 15 mm or more is preferable because it is at a level that is not problematic for use as a packaging material. In addition, when the laminate strength is high, the sealant film may be stretched or cut at the time of measurement and may not be peeled off. Such a phenomenon can be said to be the most preferable state as a laminated state.

Reference example 1
Production of acid-modified olefin elastomer (P-1) After 200 g of ethylene-propylene copolymer olefin elastomer (Tafmer P-0680 manufactured by Mitsui Chemicals, Inc.) was heated and melted in a four-necked flask under a nitrogen atmosphere, While stirring at a temperature of 170 ° C., 1.0 g of maleic anhydride and 1.0 g of dicumyl peroxide as a radical generator were respectively added over 1 hour, and then reacted for 1 hour. After completion of the reaction, the obtained reaction product was put into a large amount of acetone to precipitate a resin. This resin was further washed several times with acetone to remove unreacted maleic anhydride, and then dried under reduced pressure in a vacuum dryer to obtain an acid-modified olefin elastomer (P-1).

Reference example 2
Production of acid-modified olefin elastomer (P-2) In Reference Example 1, the same operation was performed except that the addition amount of maleic anhydride was changed to 30.0 g and the addition amount of dicumyl peroxide was changed to 6.0 g. An acid-modified olefin elastomer (P-2) was obtained.

  Table 1 shows the characteristics of the resin obtained by the above production method and the resin used in the following Reference Examples.

Reference example 3
Production of acid-modified olefin elastomer solution (S-1) 15.0 g of propylene-butene copolymer acid-modified olefin elastomer (Tafmer MP0620 manufactured by Mitsui Chemicals) and 285 g of toluene (manufactured by Nacalai Tesque) can be sealed with a heater. The mixture was placed in a glass container and heated while stirring at a rotation speed of 500 rpm. Stirring was performed until the acid-modified olefin elastomer resin was completely dissolved in a state where the temperature in the system was raised to 80 ° C., and after cooling, an acid-modified olefin elastomer solution (S-1) was obtained. The ratio of the solid content contained in the solution was 5% by mass.

Reference example 4
Production of acid-modified olefin elastomer solution (S-2) In Reference Example 3, the acid-modified olefin elastomer was changed to an acid-modified olefin elastomer of ethylene-butene copolymer (Tafmer MH5020 manufactured by Mitsui Chemicals) as the acid-modified olefin elastomer. Operation was performed to obtain an acid-modified olefin elastomer solution (S-2).

Reference Example 5
Production of acid-modified olefin elastomer solution (S-3) In Reference Example 3, the acid-modified olefin elastomer was changed to an acid-modified olefin elastomer of ethylene-butene copolymer (Tafmer MH7020 manufactured by Mitsui Chemicals) as the acid-modified olefin elastomer. Operation was performed to obtain an acid-modified olefin elastomer solution (S-3).

Reference Example 6
Production of Acid-Modified Olefin Elastomer Solution (S-4) In Reference Example 3, the same operation was performed except that the acid-modified olefin elastomer (P-1) obtained in Reference Example 1 was used as the acid-modified olefin elastomer. An acid-modified olefin elastomer solution (S-4) was obtained.

Reference Example 7
Production of acid-modified olefin elastomer aqueous dispersion (S-5) 60.0 g of acid-modified olefin elastomer (P-2), 45. 0 g of ethylene glycol-n-butyl ether (manufactured by Wako Pure Chemical Industries, special grade, boiling point 171 ° C.), 6.9 g (1.0 times equivalent to the carboxyl group of the maleic anhydride unit in the resin) of N, N— Dimethylethanolamine (manufactured by Wako Pure Chemical Industries, special grade, boiling point 134 ° C.) and 188.1 g of distilled water were charged into a glass container and stirred at a rotation speed of a stirring blade of 300 rpm. It was not recognized and it was confirmed that it was floating. Therefore, while maintaining this state, the heater was turned on and heated after 10 minutes. Then, the system temperature was kept at 140 ° C. and further stirred for 60 minutes. Then, after cooling to room temperature (about 25 ° C.) while stirring with air rotation at 300 rpm, pressure filtration (air pressure 0.2 MPa) with a 300 mesh stainless steel filter (wire diameter 0.035 mm, plain weave) As a result, a milky yellow uniform acid-modified olefin elastomer aqueous dispersion (S-5) was obtained. There was almost no residual resin on the filter.

Reference Example 8
Production of Olefin Elastomer Solution (S-6) In Reference Example 3, the same operation except that an olefin elastomer of ethylene-propylene copolymer (Tafmer P-0680 manufactured by Mitsui Chemicals) was used in place of the acid-modified olefin elastomer. To obtain an olefin elastomer solution (S-6).

Reference Example 9
Production of Acid-Modified Polyolefin Aqueous Dispersion (S-7) Acid-modified propylene resin (Yumex 1001 manufactured by Sanyo Chemical Co., Ltd., acid value 26 mgKOH / g) using a stirrer equipped with a heat-resistant 1-liter glass container with a heater 60 g, N, N-dimethylethanolamine 6.3 g, organic solvent isopropanol 60 g and distilled water 174 g were charged, sealed, and heated to 160 ° C. (internal temperature) while stirring at 300 rpm. After holding at 160 ° C. for 1 hour under stirring, the heater was turned off and cooled naturally to room temperature with stirring. After cooling, the liquid component in the flask was filtered with a 300 mesh stainless steel filter (wire diameter 0.035 mm, plain weave) And pressure filtration (air pressure 0.2 MPa) to obtain a slightly yellow and translucent uniform acid-modified polyolefin aqueous dispersion (S-7). The ratio of the solid content contained in the aqueous dispersion was 20% by mass.

Reference Example 10
Production of amino group-modified olefin elastomer solution (S-8) In Reference Example 3, amino acid-modified olefin elastomer (Dynalon 8630P manufactured by JSR) was used in place of acid-modified olefin elastomer to perform the same procedure. A group-modified olefin elastomer solution (S-8) was obtained.

  Table 2 shows the types and concentrations of resins and media for the solutions and dispersions produced by the above method.

Example 1
Using a biaxially stretched polyester resin film (Embret S-12 manufactured by Unitika Co., Ltd.) with a thickness of 12 μm and using a gravure coater, a two-component curing type polyurethane adhesive (Toyo Morton Co., Ltd.) on the corona surface of the polyester resin film Manufactured) was applied and dried so that the coating amount after drying was 5 g / m ^2, and a barrier base material was obtained in which an aluminum foil having a thickness of 7 μm was bonded as a barrier layer.
Next, the acid-modified olefin elastomer solution (S-1) was applied to the aluminum foil surface of the barrier base material so that the coating amount after drying was 0.5 g / m ^2, and was dried at 100 ° C. for 1 minute for adhesion. A layer was formed.
Next, using a laminator equipped with an extruder, a laminate in which a sealant layer composed of a 35 μm polypropylene layer is formed by melt-extrusion of polypropylene (Novatech PP FL02A manufactured by Nippon Polypro Co., Ltd.) as a sealant resin on the surface of the adhesive layer is formed. Obtained. At this time, the temperature of the sealant resin extruded from the T-die was 240 ° C.

Examples 2-5, Comparative Examples 1-3
Instead of the acid-modified olefin elastomer solution (S-1) in Example 1, (S-2), (S-3), (S-4), acid-modified olefin elastomer aqueous dispersion (S-5), respectively. A laminate was obtained by performing the same operation except that the olefin elastomer solution (S-6), the acid-modified polyolefin aqueous dispersion (S-7), and the amino group-modified olefin elastomer solution (S-8) were used.

Example 6
A laminate was obtained in the same manner as in Example 1 except that the coating amount of the adhesive layer was changed to 0.1 g / m ² .

Examples 7-8
In Example 6, it replaced with the acid modification olefin elastomer solution (S-1), and performed the same operation except having used (S-2) and (S-3), respectively, and obtained the laminated body.

Example 9
The acid-modified olefin elastomer solution (S-1) is applied to the barrier layer surface (deposition surface) of an aluminum vapor deposition film (Metaline ML-PET manufactured by Tosero Co., Ltd.) so that the coating amount after drying is 0.5 g / m ^2. And dried at 100 ° C. for 1 minute to form an adhesive layer.
Next, using a laminator equipped with an extruder, a laminate in which a sealant layer composed of a 35 μm polypropylene layer is formed by melt-extrusion of polypropylene (Novatech PP FL02A manufactured by Nippon Polypro Co., Ltd.) as a sealant resin on the surface of the adhesive layer is formed. Obtained. At this time, the temperature of the sealant resin extruded from the T-die was 240 ° C.

Examples 10-12
In Example 9, instead of the acid-modified olefin elastomer solution (S-1), (S-2), (S-3) and an acid-modified olefin elastomer aqueous dispersion (S-5) were used, respectively. The same operation was performed to obtain a laminate.

Example 13
In Example 9, it replaced with the aluminum vapor deposition film, and obtained the laminated body by the same operation except having used the alumina vapor deposition film (GL-AE by the letterpress printing company).

Example 14
In Example 1, it replaced with the polypropylene of sealant resin, and performed the same operation except having used polyethylene (Novatec LD LC600A by Nippon Polyethylene Co., Ltd.), and obtained the laminated body.

Examples 15-16
In Example 14, it replaced with the acid modification olefin elastomer solution (S-1), and performed the same operation except having used (S-2) and (S-3), respectively, and obtained the laminated body.

Example 17
Using a biaxially stretched polyester resin film (Embret PET-12 manufactured by Unitika Co., Ltd.) with a thickness of 12 μm and using a gravure coater, a two-component curing type polyurethane adhesive (Toyo Morton) on the corona-treated surface of the polyester resin film Co., Ltd.) was applied and dried so that the coating amount after drying was 5 g / m ² to obtain a barrier base material on which an aluminum foil having a thickness of 7 μm was bonded as a barrier layer.
Next, the acid-modified olefin elastomer solution (S-1) was applied to the aluminum foil surface of the barrier base material so that the coating amount after drying was 3.0 g / m ^2, and dried at 100 ° C. for 1 minute for adhesion. A layer was formed.
Next, a 50 μm unstretched polypropylene film (manufactured by Toray Industries Inc.) was passed through a nip roll heated to 120 ° C. through an adhesive layer to obtain a laminated film.

Example 18
In Example 17, a laminate was obtained by performing the same operation except that (S-4) was used instead of the acid-modified olefin elastomer solution (S-1).

  Table 3 shows the result of measuring the laminate strength of the obtained laminate.

As in Examples 1 to 18, the laminate using the acid-modified olefin elastomer as the adhesive layer showed good laminate strength and had sufficient laminate strength for use as a packaging material.
On the other hand, when a resin outside the scope of the present invention is used for the adhesive layer, that is, when an olefin elastomer that is not acid-modified is used (Comparative Example 1), when a resin that is acid-modified but is not an olefin elastomer is used. (Comparative Example 2) When the olefin elastomer modified other than acid modification is used (Comparative Example 3), the obtained laminate has a low laminate strength and cannot be used as a packaging material. It was. In Comparative Example 2, when the temperature of the sealant resin extruded from the T-die was set to 290 ° C. and laminated at a higher temperature than other examples and comparative examples, an improvement in laminate strength was observed. However, the polypropylene was thermally decomposed, and the thermally decomposed material remained in the sealant layer.

Claims (6)

A barrier layer, an adhesive layer, and a sealant layer are laminated in this order. The adhesive layer contains an acid-modified olefin elastomer, and the olefin elastomer constituting the acid-modified olefin elastomer is an ethylene / α-olefin copolymer elastomer. contains at least one of propylene · alpha-olefin copolymer elastomer, the amount of the adhesive layer is a laminate and wherein the scope der Rukoto of 0.001 to 5 g / m ^2. The laminate according to claim 1, wherein the barrier layer contains aluminum. The laminate according to claim 1 or 2 , wherein the sealant layer contains a polyolefin resin. The laminate according to claim 3 , wherein the polyolefin resin is polypropylene. When manufacturing the laminated body in any one of Claims 1-4, on the barrier layer in which the contact bonding layer containing an acid-modified olefin elastomer was formed, the melted sealant resin was passed through the contact bonding layer. A method for producing a laminate, wherein lamination is performed by extrusion lamination. When producing the laminate according to any one of claims 1 to 4 , an adhesive layer containing an acid-modified olefin elastomer is formed on the barrier layer, and then melted through the adhesive layer. Is laminated by extrusion lamination. A method for producing a laminate.