JP2008230198A - Packaging material - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a packaging material having an excellent resistance to various content. <P>SOLUTION: In a method for producing the packaging material, the packaging material is produced by laminating a barrier layer, an adhesive layer, and a sealant layer in turn. The adhesive layer is made of an acid-modified polyolefin resin having a melt flow rate at 190°C and under 2,160 g load of 50 g/min or below. The quantity of the adhesive layer is 0.001-5 g/m<SP>2</SP>. On the barrier layer, the adhesive layer made of the acid-modified polyolefin resin is formed so that its quantity is 0.001-5 g/m<SP>2</SP>. Next, a molten sealant resin is laminated on the adhesive layer by extrusion lamination. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a packaging material, and particularly relates to a packaging material having excellent content resistance.

As a packaging material, a material having a structure in which a polyolefin resin film is laminated as a sealant layer on the upper surface of a barrier layer such as an aluminum foil is often used. In general, when a sealant layer is laminated, an adhesive layer (also referred to as a primer or an anchor coat) is provided. In a bag using such packaging materials, volatile substances such as menthol and naphthalene, contents containing scent ingredients and medicinal ingredients, secondary batteries containing solid organic electrolytes, etc. were packaged. In this case, during storage, these substances and components swell or dissolve the adhesive layer between the barrier layer and the sealant layer, so that the adhesive strength between the barrier layer and the sealant layer decreases with time, There was a problem that both layers peeled off (delamination). Conventionally, in order to solve this problem, improvements shown in Patent Documents 1 and 2 have been made, but depending on the type of contents, the adhesive layer has not been sufficiently resistant.
JP-A-11-254595 JP 2001-322221 A

  The present invention is intended to provide a packaging material with improved resistance to various contents against the above problems.

  As a result of intensive studies to solve the above problems, the present inventors have used a polyolefin resin having a specific composition as an adhesive layer, and in a packaging material laminated as an adhesive layer between a barrier layer and a sealant layer, The inventors have found that the content resistance is remarkably improved, and have reached the present invention.

That is, the gist of the present invention is, firstly, a packaging material in which a barrier layer, an adhesive layer and a sealant layer are laminated in this order, and the adhesive layer has a melt flow rate of 50 g / min at 190 ° C. and a load of 2160 g. The packaging material is characterized by comprising an acid-modified polyolefin resin, and the amount of the adhesive layer is in the range of 0.001 to 5 g / m ^2. Second, on the barrier layer, 190 ° C. An adhesive layer made of an acid-modified polyolefin resin having a melt flow rate under a load of 2160 g of 50 g / min or less is formed so that the amount is in the range of 0.001 to 5 g / m ² , and then the adhesive layer is interposed A method for producing a packaging material, wherein melted sealant resin is laminated by extrusion lamination.

  The packaging material of the present invention has excellent resistance to various contents, and even when stored for a long period of time, the decrease in laminate strength is small. Therefore, the contents can be shielded from liquid or gas for a long period of time, and the commercial value of the contents is not impaired.

  The present invention will be described in detail below.

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

  Examples of the barrier layer 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. Moreover, the organic barrier layer which consists of a vinylidene chloride resin, a modified polyvinyl alcohol, an ethylene vinyl alcohol copolymer, MXD nylon etc. can be illustrated.

  In order to laminate the vapor deposition 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., manufactured by Toppan Printing Co., Ltd. “GL, GX Series”, “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, Oike Industry Co., Ltd. “MOS”, “Tetrait”, “Bebright” and the like can be exemplified. A protective coating layer may be provided on the vapor deposition layer.

  In order to laminate the organic barrier layer, there are a method of coating a film with a coating containing a resin having a barrier property, a method of laminating the resin by a co-extrusion method, etc., which also have a commercially available organic barrier layer. A method using a film 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 is appropriately selected depending on the use such as the contents to be packaged and the storage period. In general, the water vapor permeability is preferably 100 g / m ² · day (40 ° C., 90% RH) or less, preferably 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 further preferably 10 ml / m ² · day · MPa or less. 1 ml / m ² · day · MPa or less is particularly preferable.

  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.

  For the adhesive layer, an acid-modified polyolefin resin having a melt flow rate at 190 ° C. and a load of 2160 g of 50 g / min or less is used.

  The olefin component that is the main component of the acid-modified polyolefin resin is not particularly limited, but an alkene having 2 to 6 carbon atoms such as ethylene, propylene, isobutylene, 2-butene, 1-butene, 1-pentene, 1-hexene is preferable, Mixtures of these may be used. Among these, alkene having 2 to 4 carbon atoms such as ethylene, propylene, isobutylene and 1-butene is more preferable, ethylene and propylene are further preferable, and ethylene is most preferable.

  The acid-modified polyolefin resin is acid-modified with an unsaturated carboxylic acid component. Examples of unsaturated carboxylic acid components 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. It is done. Of these, acrylic acid, methacrylic acid, maleic acid, and maleic anhydride are preferable, and acrylic acid and maleic anhydride are particularly preferable. 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 content of the unsaturated carboxylic acid component is preferably 0.01 to 15% by mass, more preferably 0.1 to 12% by mass, and 0.5 to 5% by mass from the balance of adhesiveness between the barrier layer and the sealant layer. % Is more preferable, and 1-4 mass% is particularly preferable. When the content is less than 0.01 mass, sufficient adhesion with a barrier layer such as an aluminum foil may not be obtained. Moreover, when it exceeds 15 mass%, adhesiveness with a sealant layer may fall, or the water resistance of an adhesive layer may fall.

  The acid-modified polyolefin resin used for the adhesive layer preferably contains a (meth) acrylic acid ester component from the viewpoint of good adhesion to the barrier layer and the sealant layer. Examples of the (meth) acrylic acid ester component include an esterified product of (meth) acrylic acid and an alcohol having 1 to 30 carbon atoms, and (meth) acrylic acid and carbon number 1 from the viewpoint of easy availability. Esterified products with ˜20 alcohols are preferred. Specific examples of the (meth) acrylic acid ester component include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, hexyl (meth) acrylate, (meth ) Octyl acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, octyl (meth) acrylate, dodecyl (meth) acrylate, stearyl (meth) acrylate, and the like. Mixtures of these may be used. Among these, from the viewpoint of easy availability and adhesiveness, methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, hexyl acrylate, octyl acrylate are more preferable, ethyl acrylate, More preferred is butyl acrylate, and particularly preferred is ethyl acrylate. ("(Meth) acrylic acid" means "acrylic acid or methacrylic acid".)

  The content of the (meth) acrylic acid ester component in the acid-modified polyolefin resin is preferably from 0.1 to 20% by mass, and particularly preferably from 3 to 15% by mass, from the viewpoint of improving adhesiveness. When the content of the (meth) acrylic acid ester component is less than 0.1% by mass, the adhesiveness with the aluminum foil or the polyolefin resin film tends to decrease, and when it exceeds 20% by mass, the content resistance decreases. Tend to. Further, the (meth) acrylic acid ester component may 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 grafting. Examples include copolymerization (graft modification).

  The adhesive layer may contain a small amount (20% by mass or less) of a resin other than the acid-modified polyolefin resin. Examples of other resins include polyvinyl acetate, ethylene-vinyl acetate copolymer, polyvinyl chloride, polyvinylidene chloride, ethylene- (meth) acrylic acid 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, urethane resin, phenol resin, silicone resin, epoxy resin, etc. Is mentioned. The number average molecular weight of these other resins is preferably 10,000 or more, more preferably 30,000 or more, from the viewpoint of content resistance.

  The adhesive layer may contain a crosslinking agent for crosslinking the acid-modified polyolefin resin. Examples of the crosslinking agent include isocyanate compounds, melamine compounds, urea compounds, epoxy compounds, carbodiimide compounds, oxazoline group-containing compounds, aziridine compounds, zirconium salt compounds, silane coupling agents, and the like. These contents may be appropriately determined in consideration of the content resistance.

The amount of the adhesive layer needs to be in the range of 0.001 to 5 g / m ^{2 with} respect to the area of the adhesive surface, preferably 0.01 to 3 g / m ² , and 0.02 to ² g / m ^2. m ² is more preferable, 0.03 to 1 g / m ² is further preferable, and 0.05 to 1 g / m ² is particularly preferable. If it is less than 0.001 g / m ² , sufficient content resistance cannot be obtained, and if it exceeds 5 g / m ² , not only is it economically disadvantageous, but there is a concern that the amount of adsorbed content will increase.

  The acid-modified polyolefin resin used for the adhesive layer has better content resistance as the molecular weight is higher. Accordingly, the melt flow rate at 190 ° C. and 2160 g load, which is a measure of molecular weight, needs to be 50 g / min or less, preferably 0.01-30 g / 10 min, more preferably 0.1-20 g / 10 min, 0.5 to 10 g / 10 min is particularly preferable. If the melt flow rate exceeds 50 g / min, the resistance to physical properties tends to decrease, and if it is less than 0.01 g / min, there are restrictions on the production surface when the resin has a high molecular weight.

  For the sealant layer of the packaging material of the present invention, conventionally known sealant resins can be used, for example, polyethylene such as low density polyethylene (LDPE) and high density polyethylene (HDPE), acid-modified polyethylene, polypropylene, acid-modified polypropylene, Examples include polyolefin resins such as copolymer polypropylene, ethylene-vinyl acetate copolymer, ethylene- (meth) acrylic acid ester copolymer, ethylene- (meth) acrylic acid copolymer, and ionomer. Polyethylene resin is preferred, and polyethylene is particularly preferred because it is inexpensive.

  The method for providing the sealant layer is not particularly limited, but a method of bonding the sealant film made of the above-described sealant resin and the adhesive layer by heat (thermal lamination, dry lamination) or extruding and pasting the resin melted in the adhesive layer. A method of matching (extrusion lamination) and the like can be mentioned.

  In the present invention, the method for providing the adhesive layer is not particularly limited. For example, an acid-modified polyolefin resin is dissolved or dispersed to form a coating agent, which is applied to the barrier layer and the medium is dried. A method of transferring a resin layer obtained by applying a coating agent in which a modified polyolefin resin is dissolved or dispersed and drying the medium onto the barrier layer, a method of melt-extruding the acid-modified polyolefin resin onto the barrier layer using a T-die, etc. Can be mentioned. Among these, from the viewpoint of environment and performance, a method in which an aqueous dispersion in which an acid-modified polyolefin resin is dissolved or dispersed in an aqueous medium is applied to the barrier layer as an aqueous adhesive and the medium is dried is an adhesive layer. It is preferable because the amount of the acid-modified polyolefin resin can be easily adjusted, and particularly, the thickness can be easily controlled thinly. When using a water-based adhesive, there is a method in which a water-based adhesive is applied to a barrier layer, dried to form an adhesive layer, and then the sealant layer is laminated by melt extrusion (extrusion lamination) of the sealant resin in-line. It is simple and is a particularly preferred method.

  Examples of the aqueous dispersion of the acid-modified polyolefin resin suitable for the above method include those described in International Publication No. 02/055598.

  When using a water-based adhesive, the application method may be a known method such as gravure roll coating, reverse roll coating, wire bar coating, lip coating, air knife coating, curtain flow coating, spray coating, dip coating, or brush coating. The substrate surface is uniformly coated by these methods, and is set at around room temperature as necessary, and then subjected to a drying treatment or a heat treatment for drying, thereby forming a uniform adhesive layer as a barrier layer. It can be formed in close contact with the surface.

  In the case of using an aqueous adhesive, it is preferable to use an emulsifier or a compound having a protective colloid action as little as possible, and most preferably not to use, in order not to lower the content resistance.

  In the present invention, the method for laminating the sealant layer via the adhesive layer is not particularly limited. For example, the method of laminating the adhesive layer and the sealant resin film by heat, melting the sealant resin and extruding it onto the adhesive layer, cooling Examples thereof include a method of solidifying and laminating (extrusion lamination method). Among these, the extrusion lamination method is preferable from the viewpoint of reducing the thickness of the adhesive layer and resistance to contents.

  The packaging material of the present invention is usually used with the barrier layer on the outside and the sealant layer on the inside (content side). In addition, when considering the use of the packaging material or the rigidity and durability required for the packaging material, 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 preferably used in the step as a laminate with the substrate.

  Examples of the thermoplastic resin film used as the substrate 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- Polyamide resin films such as nylon and poly-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 / ethylene-vinyl alcohol copolymer / nylon 6), mixtures, and the like, 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. In addition, 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 may be 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, You may laminate | stack the film which has easy tear property and hand cut property in order to improve hand cut property.

  The method for laminating the barrier layer and the base material is not particularly limited, but for example, a known adhesive such as a two-component mixed adhesive in which a main component having a hydroxyl group or a carboxyl group and an isocyanate compound are mixed may be used. it can. 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.

  Examples of forms when making bags as the packaging material of the present invention include three-side seal bags, four-side seal bags, gusset packaging bags, pillow packaging bags, and the like. It can also be a packaging bag.

  Since the packaging material of the present invention has good resistance to various contents, it is particularly suitable as a packaging material for volatile contents. Among them, fragrance ingredients, spice ingredients, medicinal ingredients are preferred. It is most suitable as a packaging material for products. Specifically, fragrance, fragrance, bathing agent, spice, poultice, medicine, secondary battery, toiletry product, surfactant, shampoo, rinse, detergent, insect repellent, insecticide, deodorant, hair restorer, It is suitably used for vinegar, toothpaste, and cosmetic packaging materials.

  The details of the cause of the decrease in adhesive strength between layers in a barrier packaging material are unclear, but the adhesive layer is formed by the volatile components of the contents being shielded by the barrier layer and accumulating near the interface between the barrier layer and the adhesive layer. This is considered to cause deterioration such as swelling and dissolution. By using an adhesive layer having a specific composition such as the packaging material of the present invention, it is presumed that the deterioration thereof was reduced and as a result, good content resistance was obtained.

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

(1) Content of acid component of acid-modified polyolefin resin 0.5 g of polyolefin resin was dissolved in 50 ml of toluene / ethanol = 10/1 (volume ratio), titrated with methanolic KOH, and consumed for neutralization. The amount of acidic groups in the polyolefin resin was determined from the number of mg of KOH.

(2) Melt flow rate (MFR) of acid-modified polyolefin resin
It measured by the method of JIS6730 description (190 degreeC, 2160g load).

(3) Amount of adhesive layer (coating amount)
A predetermined amount of an aqueous dispersion of acid-modified polyolefin resin was applied to a substrate whose area and mass were measured in advance, and dried at 100 ° C. for 2 minutes. 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.

(4) Laminate strength (before content resistance test)
A test piece having a width of 15 mm is taken from the laminate film, and the interface between the barrier layer and the sealant layer is peeled off from the end of the test piece by a T-peel method using a tensile tester (precision universal material tester type 2020 manufactured by Intesco). 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 5 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 and cut at the time of measurement, and peeling may be impossible. Such a phenomenon is most preferable as a laminate state, and the laminate strength is 10N. / 15 mm.

(5) Content resistance test Using two 10cm square laminate films, with the polyolefin resin layer of the laminate film inside, put absorbent cotton soaked with 1g of acetic acid as the contents, heat seal all sides with a seal width of 10mm This was sealed and stored at 50 ° C. for 2 weeks. In place of 1 g of acetic acid as a content, 1 g of L-menthol and 1 g of limonene were sealed and stored in the same manner. Thereafter, each sealed packaging material was opened, and a test piece was taken from the laminate film of the packaging material in the same manner as in (4) above, and the laminate strength was measured.

(6) Tearability
When opening the bag after the content-resistant test of L-menthol, the situation when it was cut and torn by hand was visually evaluated.
○: Good tearability and no peeling between films
X: Poor tearability and peeling between films

The gas barrier performance of the films used in Examples and Comparative Examples is as follows.
・ Aluminum vapor-deposited film (Metaline ML-PET manufactured by Tosero)
Oxygen permeability: 10 ml / m ² · day · MPa (JIS K7126)
Water vapor transmission rate: 1 g / m ² · day (JIS Z0208)
・ Silica vapor deposited film (Mitsubishi Resin Tech Barrier VX)
Oxygen permeability: 5 ml / m ² · day · MPa (25 ° C., 90% RH)
Water vapor transmission rate: 0.5 g / m ² · day (40 ° C., 90%)
・ Alumina deposition film (GL-AE manufactured by Toppan Co., Ltd.)
Oxygen permeability: 5 ml / m ² · day · MPa (30 ° C., 70% RH)
Water vapor permeability: 0.6 g / m ² · day (40 ° C., 90% RH)
・ Barrier film (Embret DC KPT manufactured by Unitika)
Oxygen permeability: 95 ml / m ² · day · MPa (20 ° C., 65% RH)
Water vapor transmission rate: 13 g / m ² · day (40 ° C., 90% RH)

Reference example 1
[Production of acid-modified polyolefin resin aqueous dispersion E-1]
60.0 g of acid-modified polyolefin resin (Arkema Bondin LX-4110, maleic anhydride copolymer polyethylene resin), 90.0 g When isopropanol, 3.0 g of triethylamine and 147.0 g of distilled water were charged into a glass container and stirred at a rotation speed of the stirring blade of 300 rpm, no precipitation of resin particles was observed at the bottom of the container. It was confirmed that Therefore, while maintaining this state, the heater was turned on and heated after 10 minutes. The system temperature was kept at 140 ° C. and the mixture was further stirred for 30 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) Thus, a milky white uniform acid-modified polyolefin resin aqueous dispersion E-1 (solid content concentration 20% by mass) was obtained.

Reference example 2
[Production of acid-modified polyolefin resin aqueous dispersion E-2]
60.0 g of acid-modified polyolefin resin (Mitsui / DuPont Chemicals Nucrel N1560, ethylene-methacrylic acid copolymer), 90.0 g using a stirrer equipped with a heater and a pressure-resistant 1-liter glass container. Of isopropanol, 12.0 g of triethylamine and 138.0 g of distilled water were charged into a glass container and stirred at a rotation speed of the stirring blade of 300 rpm. It was confirmed that 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 3 hours. 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) Thus, a milky white uniform acid-modified polyolefin resin aqueous dispersion E-2 (solid content concentration 20% by mass) was obtained.

Reference example 3
[Production of acid-modified polyolefin resin solution Y-1]
Using a stirrer equipped with a hermetically sealed 1 liter glass container equipped with a heater, 10.0 g of acid-modified polyolefin resin (Nippon Polyethylene Rexpearl ET530H, maleic anhydride-modified polyethylene resin), 290 g of toluene in glass The mixture was placed in a container and kept at 110 ° C. with stirring to further stir for 30 hours to dissolve the polyolefin resin to obtain an acid-modified polyolefin resin solution Y-1 (solid content concentration: 3.3% by mass).

The composition of the acid-modified polyolefin resin used for the production of the aqueous dispersions E-1 and E-2 and the solution Y-1 is as follows.
(1) Bondine LX-4110
Ethylene / ethyl acrylate / maleic anhydride = 91/7/2 (mass%). Melt flow rate: 5 g / 10 min.
(2) Nukurel N1560
Ethylene / methacrylic acid = 85/15 (mass%). Melt flow rate: 60 g / 10 min.
(3) Lexpearl ET530H
Ethylene and methyl acrylate are included as copolymerization components, and maleic anhydride is 2.5% by mass. Melt flow rate: 30 g / 10 min.

Example 1
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 Co., Ltd.) 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, a 10% diluted solution of the acid-modified polyolefin resin aqueous dispersion E-1 was applied to the aluminum foil surface of the barrier base material so that the coating amount after drying was 0.8 g / m ^2, and ² at 100 ° C. The adhesive layer was formed by drying for a minute. Next, using a laminating apparatus equipped with an extruder, LDPE (L211 manufactured by Sumitomo Chemical Co., Ltd.) is melt-extruded as a sealant resin on the surface of the adhesive layer to obtain a laminate film in which a sealant layer composed of a 30 μm LDPE layer is formed. It was.

Examples 2 and 3
Example 1 was used in Example 1 except that E-1 was diluted and the coating amount of the adhesive layer was changed to 0.08 g / m ² (Example 2) and 0.01 g / m ² (Example 3). A laminate film was obtained in the same manner as described above.

Example 4
In Example 1, a laminate film was obtained in the same manner as in Example 1, except that an ethylene-methacrylic acid copolymer (Mitsui / DuPont Chemicals Nucrel AN4228C) was used as the sealant resin.

Example 5
In Example 1, instead of the aqueous dispersion E-1, a laminate film was obtained in the same manner as in Example 1 except that the solution Y-1 was heated and applied without dilution.

Comparative Example 1
In Example 1, a laminate film was obtained in the same manner as in Example 1 except that E-2 was used instead of the acid-modified polyolefin resin aqueous dispersion E-1.

Comparative Example 2
In Example 1, a polyurethane resin was used as the adhesive layer instead of the acid-modified polyolefin resin. That is, the same operation as in Example 1 was performed using a polyurethane resin aqueous dispersion (manufactured by Asahi Denka Co., Ltd., Adekabon titer HUX380) in place of E-1, to obtain a laminate film.

Comparative Example 3
In Example 1, an adhesive layer was not formed, and LDPE was melt-extruded directly onto the aluminum foil surface of the barrier substrate to obtain a laminate film.

Comparative Example 4
In Example 4, an adhesive layer was not formed, and an ethylene-methacrylic acid copolymer was melt-extruded directly on the aluminum foil surface of the barrier substrate to obtain a laminate film.

  About the packaging material which consists of each laminate film obtained in Examples 1-5 and Comparative Examples 1-4, laminate strength and tearability were measured before and after the content resistance test. The results are shown in Table 1.

Example 6
A laminate film was obtained in the same manner as in Example 1 except that a polypropylene resin (Ultzex 1520L manufactured by Prime Polymer Co., Ltd.) was used as the sealant resin.

Example 7
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 Co., Ltd.) was applied and dried so that the coating amount after drying was 5 g / m ² to form an adhesive layer. Next, an aluminum foil having a thickness of 7 μm was bonded as a barrier layer to obtain a barrier substrate. Next, the acid-modified polyolefin resin aqueous dispersion E-1 is applied to the aluminum foil surface of the barrier substrate so that the coating amount after drying is 3 g / m ² and dried at 100 ° C. for 2 minutes to form an adhesive layer. Then, a 50 μm polyethylene film (manufactured by Tamapoly Co., Ltd.) was passed through a heated nip roll through the adhesive layer to obtain a laminated film.

Example 8
The coating amount after drying a 10% diluted solution of acid-modified polyolefin resin aqueous dispersion E-1 on the barrier layer surface (deposition surface) of an aluminum vapor deposition film (Metaline ML-PET manufactured by Tosero Co., Ltd.) is 0.4 g / m ^2. And then dried at 100 ° C. for 2 minutes to form an adhesive layer. Next, using a laminating apparatus equipped with an extruder, LDPE (L211 manufactured by Sumitomo Chemical Co., Ltd.) is melt-extruded as a sealant resin on the surface of the adhesive layer to obtain a laminate film in which a sealant layer composed of a 30 μm LDPE layer is formed. It was.

Example 9
A laminate film was obtained in the same manner as in Example 8, except that a silica vapor deposition film (Tech Barrier VX manufactured by Mitsubishi Plastics) was used instead of the aluminum vapor deposition film.

Example 10
A laminate film was obtained in the same manner as in Example 8 except that an alumina vapor deposition film (GL-AE manufactured by Toppan Printing Co., Ltd.) was used instead of the aluminum vapor deposition film.

Example 11
A laminate film was obtained in the same manner as in Example 8, except that a barrier film (Embret DC KPT manufactured by Unitika Co., Ltd.) in which an organic barrier layer was formed instead of the aluminum deposited film was used.

  About the packaging material which consists of each laminate film obtained in Examples 6-11, laminate strength and tearability were measured before and after the content resistance test. The results are shown in Table 2.

  The packaging materials in Examples 1 to 11 showed good resistance to various contents. That is, after the content resistance test, the laminate strength was 5 N / 15 mm or more, or the laminate strength was too high to be peeled off. Moreover, the tearability was also good, and it was at a level with no problem for use as a packaging material. Further, when polyethylene was used as the sealant resin, a tendency to obtain better results was recognized.

  On the other hand, when a resin outside the range of the present invention was used for the adhesive layer, the content resistance was inferior (Comparative Examples 1 and 2). In addition, when the adhesive layer was not provided, the content resistance was inferior (Comparative Examples 3 and 4).

Claims (6)

A packaging material in which a barrier layer, an adhesive layer, and a sealant layer are laminated in this order, wherein the adhesive layer is made of an acid-modified polyolefin resin having a melt flow rate of 190 g, a load flow rate of 50 g / min. A packaging material, wherein the amount of the layer is in the range of 0.001 to 5 g / m ² . The packaging material according to claim 1, wherein the barrier layer is aluminum. The packaging material according to claim 1 or 2, wherein the sealant layer is a polyolefin resin. The packaging material according to any one of claims 1 to 3, wherein the polyolefin resin of the sealant layer contains polyethylene or polypropylene as a main component. On the barrier layer, an adhesive layer made of an acid-modified polyolefin resin having a melt flow rate at 190 ° C. under a load of 2160 g of 50 g / min or less is formed so that the amount is in the range of 0.001 to 5 g / m ^2. Then, a melted sealant resin is laminated by extrusion lamination via the adhesive layer, and then a method for producing a packaging material. 6. The production method according to claim 5, wherein an aqueous adhesive containing an acid-modified polyolefin resin having a melt flow rate at 190 ° C. under a load of 2160 g of 50 g / min or less is applied on the barrier layer and dried. A process for producing a packaging material, characterized in that