JP5121244B2 - Bottom material with reseal function and package using the same - Google Patents

Description

  The present invention relates to a bottom material, and more particularly, to a bottom material with a reseal function suitably used for packaging foods, pharmaceuticals, and the like, and a resealable package using the same.

  Conventionally, various packages with resealing function have been used as packaging means for cosmetics and sanitary products that are repeatedly opened and resealed every time they are used, or for food and pharmaceuticals that cannot be consumed once. . This package can prevent oxidative deterioration of the contents remaining after opening, or deterioration due to moisture absorption, drying, etc. For example, a zipper type package in which a plastic zipper is laminated is known. However, although this package can be repeatedly opened and has excellent durability, a dedicated device for attaching an accessory such as a zipper to the package is necessary, and a processing step associated therewith is also necessary. There were problems such as increased manufacturing costs and reduced production efficiency.

  On the other hand, a multilayer film that can give a reseal function to the package itself without attaching an accessory such as a zipper has been developed. For example, Patent Documents 1, 2, 3, and 4 include a surface resin layer (corresponding to a layer that can be combined in Patent Document 4), a rubber thermoplastic resin, and a tackifier. A multilayer film comprising a resin layer (corresponding to a pressure-sensitive adhesive layer in Patent Document 4) and a heat seal resin layer (corresponding to a welding layer in Patent Document 4), and the lid material is peeled off from the multilayer film In particular, a bottom material made of a multilayer film that is peeled off between the adhesive resin layer and the heat seal resin layer and exposed in an adhesive state that can be resealed at the heat seal portion is disclosed.

  However, when these multilayer films are used as the bottom material of a package, it is necessary to appropriately select a resin to be used for the heat seal resin layer depending on the material of the heat seal part of the lid material to be sealed. Depending on the type of resin selected for the heat seal resin layer, there is a possibility that good resealability may not be obtained when resealing a package that has been resealed with the adhesive resin layer and the heat seal resin layer overlapped. .

  Further, in these packages, since the adhesive resin layer and the heat seal resin layer are directly adjacent to each other, additives such as lubricants and antiblocking agents added to the heat seal resin layer after opening are exposed over time. There is a concern that the reseal peel strength with the adhesive resin layer may decrease due to bleeding on the surface of the heat seal resin layer.

  Patent Document 5 discloses a heat-sealing packaging material in which an adhesive resin layer (adhesive layer) and a heat sealant layer are formed in this order on at least one surface of a substrate, and the adhesive resin layer and the A packaging material is disclosed in which the adhesive strength between the heat sealant layers is smaller than the heat seal strength between the heat sealant layer and the layer to be heat sealed.

  Specifically, as an example, on a biaxially stretched polypropylene surface of a laminate film (thickness 50 μm) made of polyester and biaxially stretched polypropylene, 10% by mass of styrene and 90% by mass of a diene hydrocarbon are formed. Heat seal in which an adhesive resin layer having a thickness of 25 μm is laminated by extrusion lamination using a random copolymer with a hydrogenated product of a random copolymer, and a solvent-soluble acrylic heat seal lacquer is further coated on the adhesive resin layer The packaging material which laminated | stacked the agent layer is illustrated. In the case of a package body cut out in a circle with a tab and heat-sealed in a polystyrene container as a lid material, if the tab is pinched and pulled, peeling occurs at the interface between the adhesive resin layer and the heat-sealant layer, and the peeling occurs It is described that when a lid is placed on a container and pressure-bonded with a finger or the like, the adhesive resin layer re-adheres to the flange portion and is sealed again.

However, the packaging body having the above structure has a process in which the adhesive resin is exposed to the outside before coating the heat sealing agent, and dust, dust, etc. floating in the atmosphere adhere to the adhesive resin. In some cases, resealability may be reduced, and special equipment such as a coater for coating and a drying equipment is required, resulting in an increase in manufacturing cost.
JP 2004-58568 A JP 2004-106878 A JP 2004-1105040 A JP 2001-10659 A JP 2005-41539 A

  The present invention has been made in order to solve the problems of conventional bottom materials, and the problems can be solved only by good easy-openability and pressure-bonding by hand or fingers regardless of the material of the sealed object. It is an object of the present invention to provide a bottom material with a resealing function which has both good resealability and a resealable package using the same.

As a result of intensive studies, the present inventors use a styrene-based thermoplastic elastomer and a tackifier as the main components of the adhesive resin layer, and dispose a release resin layer between the adhesive resin layer and the heat seal resin layer. As a result, the inventors have found that the above problems can be solved, and have completed the present invention.
That is, the subject of this invention is achieved by the following bottom material with a reseal function, and the package using the bottom material.

(1) The surface resin layer (A), the adhesive resin layer (B), the release resin layer (C) and the heat seal resin layer (D) are in the order of (A) / (B) / (C) / (D). Laminated, the adhesive resin layer (B) is a styrene thermoplastic elastomer (b1) and a tackifier (b2), the release resin layer (C) is an ester resin , and the heat seal resin layer (D) is an olefin. A resin layer and / or a styrene thermoplastic elastomer as a main component, and the total thickness of the release resin layer (C) and the heat seal resin layer (D) is 1 μm or more and 30 μm or less, Ri der thickness 0.5μm or 29.5μm or less of the release resin layer (C), used in the base material of the multilayer film characterized by being produced by coextrusion, the heat-sealing resin of the multilayer film Layer (D) to be sealed When heat-sealing the heat-seal part to heat-seal the bottom material and the cover material, and then peel off the cover material from the heat-seal part, in the heat-seal part, the adhesive resin layer (B) and the The pressure-sensitive adhesive resin layer (C) is delaminated, and the pressure-sensitive adhesive resin layer (B) is exposed in a state where it can be resealed with the pressure-release resin layer (C), and the pressure-sensitive adhesive resin layer (B) is exposed in the heat seal portion, the release resin layer (C) and the heat seal resin layer (D) are broken from the bottom material, and the adhesive resin layer (B) and the release resin layer. A re-sealable packaging body, which is formed by delamination with (C) and transfer of the release resin layer (C) and the heat seal resin layer (D) to the sealed body side.
(2) The surface resin layer (A) is at least one thermoplastic selected from the group consisting of olefin resins, amide resins, saponified ethylene-vinyl acetate copolymers, ester resins, and styrene resins. The resealable packaging body according to the above (1), which is composed mainly of a resin.
(3) The styrene thermoplastic elastomer (b1) is a hydrogenated styrene-butadiene block copolymer (SB), a hydrogenated styrene-isoprene block copolymer (SI), or a styrene-butadiene-styrene block. Copolymer (SBS) hydrogenated product, styrene-isoprene-styrene block copolymer (SIS) hydrogenated product, styrene-isoprene-butadiene-styrene block copolymer (SIBS) hydrogenated product, styrene-butadiene It is a hydrogenated product of at least one styrenic thermoplastic elastomer selected from the group consisting of a hydrogenated random copolymer (SBR) and a hydrogenated styrene-isoprene random copolymer (SIR). The resealable package according to (1) or (2) above.
(4) The above (1) to (1), wherein the tackifier (b2) is at least one tackifier selected from the group consisting of a rosin resin, a terpene resin, and a petroleum hydrocarbon resin. (3) The resealable packaging body according to any one of the above.
(5) The resealable package according to (4) above, wherein the content of the tackifier (b2) in the adhesive resin layer (B) is 2% by mass or more and 50% by mass or less.
(6) The surface resin layer (A) is composed of two or more layers, and has a layer mainly composed of a saponified ethylene-vinyl acetate copolymer and / or a layer mainly composed of an amide resin. The resealable package according to any one of (1) to (5) above.
(7) An adhesive resin composed mainly of an olefin-based adhesive resin and / or a styrene-based thermoplastic elastomer-based adhesive resin between the release resin layer (C) and the heat seal resin layer (D). The resealable package according to any one of (1) to (6) above, comprising a layer (E).
(8) The total thickness of the release resin layer (C), the adhesive resin layer (E), and the heat seal resin layer (D) is 1 μm or more and 30 μm or less, as described in (7) above Resealable packaging.

  According to the present invention, regardless of the material of the object to be sealed, a bottom material with a reseal function that has both a good easy-opening property and a good resealability only by pressure and pressure bonding by hand or finger, and The used resealable package can be provided.

Hereinafter, the bottom material with re-sealing function and the package (hereinafter referred to as “the bottom material of the present invention” and “the package of the present invention”, respectively) of the present invention will be described in detail.
In the present specification, “configured as a main component” is intended to allow other components to be included within a range that does not impede the action and effect of the resin constituting each layer. Further, this term does not limit the specific content, but it is 70% by mass or more and 100% by mass or less, preferably 85% by mass or more and 100% by mass or less, more preferably 95% by mass of the total components of each layer. It means that it occupies% or more and 100 mass% or less.

[Sole material of the present invention]
The bottom material of the present invention is such that the surface resin layer (A), the adhesive resin layer (B), the release resin layer (C) and the heat seal resin layer (D) are (A) / (B) / (C) / ( D) a bottom material using a multilayer film laminated in the order of D), wherein the adhesive resin layer (B) is composed mainly of a styrene-based thermoplastic elastomer (b1) and a tackifier (b2). When the heat-sealing resin layer (D) is heat-sealed at the heat-sealing part of the object to be sealed and then the bottom material is peeled off from the heat-sealing part, the adhesive resin layer at the heat-sealing part (B) and the release resin layer (C) are delaminated, and the adhesive resin layer (B) is exposed in a state where it can be resealed with the release resin layer (C). It is a bottom material.

First, the surface resin layer (A) of the bottom material of the present invention will be described.
The surface resin layer (A) is a layer composed of the thermoplastic resin (a) as a main component, and the delamination strength between the surface resin layer (A) and the adhesive resin layer (B) at the time of peeling is adhesive. The layer structure is not particularly limited as long as it is greater than the delamination strength between the resin layer (B) and the release resin layer (C), and may be a single layer or a multilayer.

  The thermoplastic resin (a) used as the main component of the surface resin layer (A) is the resin used as the main component of the adhesive resin layer (B), the release resin layer (C), and the heat seal resin layer (D). It is necessary to select appropriately considering the type. Since the thermoplastic resin (a) has a melt extrusion temperature in a range of approximately 180 ° C. or more and 300 ° C. or less, a thermoplastic resin that can be melt extruded within this range is suitably used. Specific examples of the thermoplastic resin (a) include olefin resins (ethylene resins, propylene resins, cyclic olefin resins, etc.), amide resins, saponified ethylene-vinyl acetate copolymers, ester resins, Examples thereof include styrene resins and carbonate resins. These thermoplastic resins can be used alone or as a mixed resin composition of two or more, and can form a single layer structure or a multilayer structure.

  In the present invention, in consideration of molding processability, production cost, transparency and the like, the thermoplastic resin (a) includes olefin resin, amide resin, saponified ethylene-vinyl acetate copolymer, ester resin, and styrene. At least one thermoplastic resin selected from the group consisting of a series resin can be suitably used.

  When the olefin resin is an ethylene resin, examples of the ethylene resin include very low density polyethylene (VLDPE), linear low density polyethylene (LLDPE), low density polyethylene (LDPE), medium density polyethylene (MDPE), and high density. Ethylene resins such as polyethylene (HDPE); ethylene-vinyl acetate copolymer (EVA), ethylene-methyl methacrylate copolymer (EMMA), ethylene-ethyl acrylate copolymer (EEA), ethylene-methyl acrylate copolymer Copolymer (EMA), ethylene-acrylic acid copolymer (EAA), ethylene-methacrylic acid copolymer (EMAA), ethylene-glycidyl methacrylate copolymer (E-GMA), ethylene-vinyl acetate-glycidyl methacrylate copolymer (E-VA-GMA), D Ethylene copolymers such as lene-maleic anhydride copolymer (E-MAH), ethylene-ethyl acrylate-maleic anhydride copolymer (E-EA-MAH); and further ethylene-acrylic acid copolymer And a neutralized metal of ethylene-methacrylic acid copolymer. These may be used alone or in combination of two or more.

  When the olefin resin is a propylene resin, examples of the propylene resin include propylene homopolymers and copolymers of propylene and other α-olefins such as ethylene and butene. Either a copolymer or a block copolymer can be used. The stereoregularity may be any of an isotactic structure, a syndiotactic structure, an atactic structure, a stereo block structure, and the like. These may be used alone or in combination of two or more.

  When the olefin resin is a cyclic olefin resin, examples of the cyclic olefin resin include random copolymers of ethylene and cyclic olefins such as norbornenes, tetracyclododecenes and derivatives thereof, cyclic olefin ring-opening polymers, or Examples thereof include cyclic olefin ring-opening copolymers, hydrogenated products of cyclic olefin ring-opening polymers or cyclic olefin ring-opening copolymers, and graft modified products of these polymers or copolymers. Here, in the case of a random copolymer of ethylene and a cyclic olefin, it may contain an α-olefin other than ethylene, or may contain butadiene, isoprene or the like as the third component. These may be used alone or in combination of two or more.

  Examples of the amide-based resin include, as aliphatic polyamide polymers, ring-opening polymers of cyclic lactams, polycondensates of aminocarboxylic acids, and polycondensates of dicarboxylic acids and diamines. Specifically, a homopolymer of ε-caprolactam referred to as 6 nylon, polyhexamethylene adipamide referred to as 66 nylon, or 6-66 nylon as a copolymer thereof can be used. Moreover, as an aromatic polyamide polymer, a resin containing 70 mol% or more of a polyamide constituent unit composed of xylylenediamine and an α, ω aliphatic dicarboxylic acid having 6 to 12 carbon atoms in the molecular chain, etc. Can be used. Specifically, homopolymers such as polymetaxylylene adipamide, polymetaxylylene pimeramide, polymetaxylylene azelamide, polyparaxylylene azelamide, polyparaxylylene decanamide, metaxylylene / paraxylylene azamide Examples of the copolymer include a amide copolymer, a metaxylylene / paraxylylene pimeramide copolymer, a metaxylylene / paraxylylene azeramide copolymer, and a metaxylylene / paraxylylene sepacamide copolymer. These may be used alone or in combination of two or more.

  The saponified ethylene-vinyl acetate copolymer has an ethylene content of 29% or more, preferably 32% or more, 47 mol% or less, preferably 44 mol% or less, and a saponification degree of 90%. Above, preferably 95% or more is suitably used. By selecting a grade in which the ethylene content and the degree of saponification are in the above ranges, the gas barrier properties and mechanical strength of the film can be improved. These may be used alone or in combination of two or more.

  Examples of the ester resin include polyethylene terephthalate resin, polypropylene terephthalate resin, polybutylene terephthalate resin, polyethylene isophthalate resin, polyethylene naphthalate resin, polybutylene naphthalate resin, polyethylene terephthalate / isophthalate copolymer resin, 1,4-cyclohexane. Represented by low crystalline or amorphous polyethylene terephthalate resin, polyethylene / neopentyl terephthalate copolymer resin, and polylactic acid-based resin containing 15 to 50 mol% of dimethanol units in all glycol monomer units. Examples include aliphatic polyester resins.

  In addition, a thermoplastic polyester elastomer having a high melting point and high crystallinity aromatic polyester as a hard segment and an amorphous polyester or amorphous polyether as a soft segment may be appropriately mixed with the ester resin. These elastomers may be used alone or in a suitable mixture of two or more.

  Examples of the styrenic resin include general-purpose polystyrene (GPPS), high impact polystyrene (HIPS), styrene- (meth) acrylic acid ester copolymer, and a styrenic copolymer composed of a styrenic monomer and a (meth) acrylic acid ester. A resin containing 1% by mass or more and 20% by mass or less of a rubber-like elastic body as dispersed particles in the continuous phase. You may use these individually by 1 type or in mixture of 2 or more types.

  The surface resin layer (A) is composed of two or more surface resin layers (A) in order to give the multilayer film functions such as gas barrier properties and pinhole resistance, and is composed of ethylene-vinyl acetate. It is preferable to have at least one layer containing a saponified polymer as a main component and / or a layer containing an amide resin as a main component. However, when the surface resin layer (A) has a multilayer structure, the delamination strength between the resin layers constituting the multilayer is the delamination strength between the adhesive resin layer (B) and the release resin layer (C). It is also important to appropriately select and use an adhesive resin that is larger than that.

  Here, as the adhesive resin, ethylene-based resins such as linear low density polyethylene (LLDPE), low density polyethylene (LDPE), and ethylene-vinyl acetate copolymer (EVA), propylene homopolymer, and Propylene resins such as copolymers of propylene and other α-olefins, monobasic unsaturated fatty acids such as acrylic acid or methacrylic acid, or methyl acrylate, methyl methacrylate, or glycidyl methacrylate An olefin-based adhesive resin in which an ester compound of a monobasic unsaturated fatty acid or an anhydride of a dibasic fatty acid such as maleic acid, fumaric acid or itaconic acid is chemically bonded is preferably used. Specific examples of such an adhesive resin include trade name “Admer” manufactured by Mitsui Chemicals, Inc. and trade name “Modic” manufactured by Mitsubishi Chemical Corporation.

  Other components may be appropriately added to the surface resin layer (A) as long as the gist of the present invention is not impaired. Specific examples include components such as an antifogging agent, an antistatic agent, a heat stabilizer, a nucleating agent, an antioxidant, a lubricant, an antiblocking agent, a release agent, and an ultraviolet absorber. When the surface resin layer (A) has a multilayer structure, it may be added only to a specific layer or may be added to all layers.

Next, the adhesive resin layer (B) of the bottom material of the present invention will be described.
The pressure-sensitive adhesive resin layer (B) is particularly limited as long as it is a pressure-sensitive adhesive resin layer composed mainly of a styrene-based thermoplastic elastomer (b1) and a tackifier (b2) and has adhesiveness. It is not a thing. The styrenic thermoplastic elastomer (b1) used here is preferably styrene, a copolymer of a styrene homologue such as α-methylstyrene and a conjugated diene, or a hydrogenated derivative thereof. Here, examples of the conjugated diene constituting the conjugated diene moiety include 1,3-butadiene, isoprene, 1,3-pentadiene, and the like. These may be used alone or in a state where two or more kinds are mixed in the copolymer. It may be included. Examples of the styrenic thermoplastic elastomer (b1) include styrene-isoprene-styrene block copolymer (SIS), styrene-butadiene-styrene block copolymer (SBS), and styrene-isoprene-butadiene-styrene copolymer (SIBS). ), Styrene block copolymers such as styrene-isoprene block copolymer (SI), styrene-butadiene block copolymer (SB), hydrogenated products of these styrene block copolymers, styrene / butadiene random copolymer Examples thereof include styrene random copolymers such as polymers (SBR) and styrene / isoprene random copolymers (SIR), and hydrogenated products of these styrene random copolymers. These may be used alone or in combination of two or more.

  Among these styrene thermoplastic elastomers, hydrogenated styrene-butadiene block copolymer (SB), hydrogenated styrene-isoprene block copolymer (SI), styrene-butadiene-styrene block copolymer (SBS). ), Hydrogenated product of styrene-isoprene-styrene block copolymer (SIS), hydrogenated product of styrene-isoprene-butadiene-styrene block copolymer (SIBS), styrene-butadiene random copolymer ( SBR hydrogenated product and styrene-isoprene random copolymer (SIR) hydrogenated product selected from the group consisting of hydrogenated products of at least one styrenic thermoplastic elastomer have excellent thermal stability during molding. It can be used suitably in terms of suppressing the generation of deteriorated products and the generation of odors. The The hydrogenation ratio of the hydrogenated product of these styrenic thermoplastic elastomers is preferably such that hydrogen is added to 80% or more, preferably 95% or more of the double bonds. The styrene content of the hydrogenated product of these styrene-based thermoplastic elastomers is 1% by mass or more, preferably 3% by mass or more, more preferably 5% by mass or more, and 40% by mass or less, preferably 20% by mass. Hereinafter, it is more preferably 15% by mass or less from the viewpoint of resealability between the pressure-sensitive adhesive resin layer (B) and the release resin layer (C) and thermal stability during molding. Specific examples of such a styrenic thermoplastic elastomer include the product names “Hibler 7311” and “Septon 2063” manufactured by Kuraray Co., Ltd., the product names “Tuftec H1221” manufactured by Asahi Kasei Co., Ltd., and JSR Corp. Product name “Dynalon 1320P” or the like.

  The tackifier (b2) may be a natural resin or synthetic resin that has adhesiveness at room temperature, and may be natural resin rosin, polymerized rosin, hydrogenated rosin, rosin pentaerythritol ester, and rosin glycerin. Rosin resins such as esters; terpene resins such as terpene / phenol resins, terpene resins (α-pinene resins, β-pinene resins), aromatic modified terpene resins and hydrogenated terpene resins; aromatic hydrocarbon resins, fats Aromatic hydrocarbon resins, aliphatic cyclic hydrocarbon resins, aliphatic / alicyclic petroleum resins, aliphatic / aromatic petroleum resins, unsaturated hydrocarbon copolymers, hydrogenated hydrocarbon resins, etc. Hydrocarbon resins; phenolic resins such as phenol / formaldehyde resins and xylene / formaldehyde resins; And chroman resins such as copper resins.

  Of these, rosin-based resins, terpene-based resins, and petroleum-based hydrocarbon resins can be suitably used because of their good compatibility with the styrene-based thermoplastic resin (b1). Specific examples of such a tackifier include trade name “Arcon P-100” manufactured by Arakawa Chemical Industries, Ltd., trade name “YS Resin PX1150” manufactured by Yasuhara Chemical Co., Ltd., and the like.

  The mass% of the tackifier (b2) contained in the adhesive resin layer (B) is 50% by mass or less, preferably 40% by mass or less, more preferably 30% by mass or less, and 2% by mass or more. , Preferably 5% by mass or more, more preferably 10% by mass or more. When the content of the tackifier (b2) is 50% by mass or less, good moldability is obtained, and when the content is 2% by mass or more, the adhesive resin layer (B) and the release resin layer are obtained. The effect of increasing the resealability with (C) appears.

  Other resins and components may be appropriately added to the pressure-sensitive adhesive resin layer (B) as long as the gist of the present invention is not impaired. Specific examples include low crystalline or amorphous olefin resins, softeners, oils (mineral oils), stabilizers (antioxidants, etc.), liquid paraffin, and the like.

Next, the release resin layer (C) of the bottom material of the present invention will be described.
The release resin layer (C) is a layer composed mainly of the thermoplastic resin (c), and the delamination strength between the adhesive resin layer (B) and the release resin layer (C) during the peeling is the surface. Especially if it is a layer structure which becomes smaller than the delamination strength between the resin layer (A) and the adhesive resin layer (B) and between the release resin layer (C) and the heat seal resin layer (D) However, it may be a single layer or multiple layers as desired.

  The thermoplastic resin (c) contained as the main component of the release resin layer (C) has a melt extrusion temperature of about 180 ° C. or higher, like the thermoplastic resin (a) constituting the main component of the surface resin layer (A). A thermoplastic resin that can be melt-extruded at 300 ° C. or lower is preferably used. Specifically, as the thermoplastic resin (c), easy-openability and resealability of the adhesive resin layer (B) mainly composed of the styrenic thermoplastic elastomer (b1) and the tackifier (b2) In view of the balance, molding processability, transparency, etc., at least one thermoplastic resin selected from the group consisting of ester resins, amide resins, cyclic olefin resins, and saponified ethylene-vinyl acetate copolymers Is mentioned.

  In the present invention, the thermoplastic resin (c) that is suitably used in the release resin layer (C) is excellent in rigidity, and the adhesive resin layer (B) by an external force at the time of delamination from the adhesive resin layer (B). And the release surface of the release resin layer (C) can be reduced in roughness, unevenness of each layer, etc., easy openability and good resealability when opening-resealing is repeated, industrially stable, In addition, it is preferable to use an ester resin or an amide resin that is available at a relatively low cost. Among these, polyethylene terephthalate resin and 1,4-cyclohexanedimethanol are excellent in moldability and transparency, and do not peel or open with a slight impact, and can be easily peeled when opening. Ester resins such as low crystalline or amorphous polyethylene terephthalate resin containing 15 mol% to 50 mol% of all glycol monomer units, 6-66 nylon, 12 nylon, terephthalic acid and isophthalic acid An amide resin such as a low crystalline or amorphous polyamide resin obtained by reacting a dicarboxylic acid such as hexamethylene diamine or isophorone diamine can be preferably used.

  Here, the polyethylene terephthalate resin can be easily obtained from each company, for example, trade name “Novapex GS600” manufactured by Mitsubishi Chemical Co., Ltd., trade name “Mitsui PET J125” manufactured by Mitsui Chemicals, etc. it can. Moreover, as an amorphous polyethylene terephthalate resin, the brand name "EASTAR PETG Copolyester6763" by Eastman Chemical Co., Ltd., the brand name "SkyGreen S2008" by SKC Ltd. etc. can be illustrated, for example.

  Examples of the amide-based resin include 6-66 nylon resin such as “Novamid 2063” manufactured by Mitsubishi Engineering Plastics Co., Ltd. and “UBE Nylon 5033B” manufactured by Ube Industries, Ltd. it can. In addition, examples of the 12 nylon resin include a product name “UBESTA 3035UF” manufactured by Ube Industries, Ltd., a product name “Grillamid L25” manufactured by Emschemy Japan Co., Ltd., and the like. Examples of the amorphous polyamide resin include trade name “Novamid X21” manufactured by Mitsubishi Engineering Plastics Co., Ltd. and trade name “Sealer PA3426” manufactured by Mitsui DuPont Polychemical Co., Ltd.

  The bottom material of the present invention is limited to the resin constituting the heat-sealed part of the sealed object by disposing the release resin layer (C) between the adhesive resin layer (B) and the heat-seal resin layer (D). Without being carried out, it is possible to impart a good initial peel strength and resealability with the adhesive resin layer (B). In the present invention, it is preferable to use, as the thermoplastic resin (c), a thermoplastic resin having an excellent initial peel strength from the adhesive resin layer (B) and resealability rather than the thermoplastic resin (d).

  Specifically, at present, as the resin constituting the heat seal portion of the object to be sealed, an olefin resin that can be heat sealed under the heat seal condition (temperature: about 120 to 180 ° C.) that is usually employed is mainly used. However, in the present invention, as the release resin layer (C) that exhibits good initial peel strength and resealability with the adhesive resin layer (B), an ester resin or an amide resin, a heat seal resin layer (D ) Can be preferably selected from layers each comprising an olefin resin and / or a styrene thermoplastic elastomer as main components.

  In addition, in the release resin layer (C), in order to develop stable resealability between the adhesive resin layer (B) and the release resin layer (C), mixing with an additive that easily bleeds on the surface of the release resin layer (C) It is preferable not to do as much as possible.

Next, the heat seal resin layer (D) of the bottom material of the present invention will be described.
The heat seal resin layer (D) is a heat sealable resin layer composed mainly of the thermoplastic resin (d). When the heat seal resin layer (D) is heat sealed at the heat seal portion of the object to be sealed and then the bottom material is peeled off from the heat seal portion, the release resin layer (C) and the heat seal resin layer (D) There is no particular limitation as long as the layer peeling strength between the adhesive resin layer (B) and the peeling resin layer (C) is greater than the interlayer peeling strength. The resin layer may be a multi-layered resin layer.

  When the thermoplastic resin (d) constituting the main component of the heat seal resin layer (D) is used by deep-drawing the bottom material of the present invention and heat-sealing with the cover material, the cover material is a sealed object. Resin that has appropriate heat seal strength in consideration of the material of the sealing surface and the type of resin used as the main component of the surface resin layer (A), adhesive resin layer (B), and release resin layer (C) Can be appropriately selected and used. Examples of the thermoplastic resin (d) include olefin resins (ethylene resins, propylene resins, etc.), styrene resins, ester resins, styrene thermoplastic elastomers, and the like. In the present invention, the release resin layer (C) and the heat seal resin layer (under a heat seal condition (temperature: about 120 to 180 ° C.) usually employed in various multilayer films are inexpensive and excellent in moldability and the like. An olefin-based resin that can make the delamination strength between D) larger than the delamination strength between the adhesive resin layer (B) and the release resin layer (C) can be suitably used.

  When the olefin-based resin is an ethylene-based resin, examples of the ethylene-based resin include very low density polyethylene (VLDPE), linear low density polyethylene (LLDPE), low density polyethylene (LDPE), medium density polyethylene (MDPE), and high density polyethylene. (HDPE) and other ethylene resins; ethylene-vinyl acetate copolymer (EVA), ethylene-methyl methacrylate copolymer (EMMA), ethylene-ethyl acrylate copolymer (EEA), ethylene-methyl acrylate copolymer (EMA), ethylene-acrylic acid copolymer (EAA), ethylene-methacrylic acid copolymer (EMAA), ethylene-glycidyl methacrylate copolymer (E-GMA), ethylene-vinyl acetate-glycidyl methacrylate copolymer ( E-VA-GMA), Ethile -Ethylene copolymers such as maleic anhydride copolymer (E-MAH), ethylene-ethyl acrylate-maleic anhydride copolymer (E-EA-MAH); and further ethylene-acrylic acid copolymer Metal neutralized products, metal-neutralized products of ethylene-methacrylic acid copolymers and the like can be mentioned. These may be used alone or in combination of two or more.

  When the olefin resin is a propylene resin, examples of the propylene resin include propylene homopolymers and copolymers of propylene and other α-olefins such as ethylene and butene. The copolymers include random copolymers. Either a polymer or a block copolymer can be used. The stereoregularity may be any of an isotactic structure, a syndiotactic structure, an atactic structure, a stereo block structure, and the like. These may be used alone or in combination of two or more.

  The styrenic thermoplastic elastomer has a styrene content of 1% by mass or more, preferably 5% by mass or more, more preferably 10% by mass or more, and 60% by mass or less, preferably 40% by mass or less, more preferably. 35% by mass or less of styrene-isoprene-styrene block copolymer (SIS), styrene-butadiene-styrene block copolymer (SBS), styrene-isoprene block copolymer (SI), styrene-butadiene block copolymer ( SB), styrene-ethylenepropylene-styrene block copolymer (SEPS), styrene-ethylenebutylene-styrene block copolymer (SEBS), styrene-ethylenepropylene block copolymer (SEP), styrene-ethylenebutylene block copolymer Combined (SEB), steel Styrene block copolymer such as ethylene-ethylenebutylene-olefin crystal block copolymer (SEBC), styrene such as styrene-butadiene random copolymer (SBR), hydrogenated styrene-butadiene random copolymer (HSBR) System random copolymers and the like. These may be used alone or in combination of two or more.

  Moreover, the heat seal resin layer (D) makes the delamination strength between the release resin layer (C) larger than the delamination strength between the adhesive resin layer (B) and the release resin layer (C). Therefore, an adhesive resin layer containing an adhesive resin as a main component between the release resin layer (C) and the heat seal resin layer (D) is contained in the heat seal resin layer (D). (E) can be arranged.

  Here, as the adhesive resin, linear resins such as linear low density polyethylene (LLDPE), low density polyethylene (LDPE), and ethylene-vinyl acetate copolymer (EVA), propylene homopolymer, and propylene Monopropylene unsaturated fatty acid such as acrylic acid or methacrylic acid, or monobase such as methyl acrylate, methyl methacrylate, or glycidyl methacrylate Olefinic Adhesive Resin with Chemically Bonded Ester Compound of Polyunsaturated Fatty Acid or Dibasic Fatty Acid Anhydride such as Maleic Acid, Fumaric Acid or Itaconic Acid, or Styrene-Ethylene Butylene-Styrene Block Copolymer Combined (SEBS) or Styrene-Ethylenebutylene-Oleph Styrenic thermoplastic elastomer-based adhesives in which polar functional groups such as carboxyl groups, acid anhydride groups, epoxy groups, and amino groups are incorporated into styrene-based thermoplastic elastomers such as polymer crystal block copolymer (SEBC) Resin is preferably used.

  As a specific example of such an adhesive resin, in the former olefin-based adhesive resin, a product name “Admer” manufactured by Mitsui Chemicals, Inc., a product name “Modic” manufactured by Mitsubishi Chemical Corporation, and the like can be exemplified. . Further, in the latter styrene thermoplastic elastomer adhesive resin, trade names “Dynalon” (8630P, 4630P) manufactured by JSR Corporation, trade names “Tuftec” (M1943, M1913) manufactured by Asahi Kasei Chemicals Corporation, etc. Can be illustrated.

  It is preferable to add a lubricant or an anti-blocking agent to the heat seal resin layer (D) as appropriate from the viewpoints of processing suitability during extrusion film formation and packaging suitability in a filling machine such as a deep drawing packaging machine. Here, when the surface resin layer (A) / adhesive resin layer (B) / heat seal resin layer (D) disclosed in Patent Document 2 are laminated in this order and the heat seal portion is peeled off, the adhesive resin layer In the multilayer film which peels between the layers of (B) and the heat seal resin layer (D), there are the following problems.

  That is, since the adhesive resin layer (B) and the heat seal resin layer (D) are directly adjacent to each other, additives such as a lubricant and an antiblocking agent added to the heat seal resin layer (D) after opening are changed over time. There is a concern that the reseal peel strength with the adhesive resin layer (B) may decrease due to bleeding on the exposed surface of the heat seal resin layer. On the other hand, when the release resin layer (C) is disposed between the adhesive resin layer (B) and the heat seal resin layer (D) and the heat seal portion is peeled off like the bottom material of the present invention. In a multilayer film that delaminates between the adhesive resin layer (B) and the release resin layer (C), additives such as lubricants and antiblocking agents that are suitably added to the heat seal resin layer (D) are delaminated portions. Since there is little influence on reseal strength, there is an advantage that stable resealability can be obtained.

  Furthermore, you may add suitably another component to the heat seal resin layer (D) in the range which does not impair the main point of this invention. Specific examples include antifogging agents, antistatic agents, heat stabilizers, nucleating agents, antioxidants, mold release agents, and ultraviolet absorbers.

  In the bottom material of the present invention, the heat-seal resin layer (D) of the bottom material is heat-sealed at the heat-sealed portion of the object to be sealed, and then the bottom material is peeled off from the heat-seal portion, the adhesive resin layer (B) In the heat seal portion, the release resin layer (C) and the heat seal resin layer (D) are broken from the bottom material, and the adhesive resin layer (B) and the release resin layer (C). As a combination of the resins selected for each layer, the adhesive resin is used as the combination of the resins selected for the respective layers, and the peeling resin layer (C) and the heat seal resin layer (D) are transferred to the sealed object side. The delamination strength between the layer (B) and the release resin layer (C) is between the surface resin layer (A) and the adhesive resin layer (B), and the release resin layer (C) and the heat seal resin layer (D). Make the structure smaller than the delamination strength between There is required. At the same time, it is also important to ensure the delamination strength to such an extent that the function as a package can be maintained so that the layers are not easily peeled off or opened by a slight impact.

  From these viewpoints, as a combination of resins selected for the adhesive resin layer (B) and the release resin layer (C), the interlayer peel strength (initial peel strength) is in the range of 1 N / 15 mm width to 20 N / 15 mm width. It is preferable to select as follows. Here, if the delamination strength is 1 N / 15 mm width or more, problems such as easy opening of the packaging body due to a slight impact are unlikely to occur, and if it is 20 N / 15 mm width or less, the packaging body Is easy because it is easy to open by hand, which is preferable.

  In the present invention, the more preferable range of the interlaminar peel strength (initial peel strength) between the adhesive resin layer (B) and the release resin layer (C) has a lower limit of 3 N / 15 mm width or more, and more preferably 5 N / 15 mm. It is not less than the width and the upper limit is not more than 15 N / 15 mm width, more preferably not more than 10 N / 15 mm width.

  Next, with regard to resealability after opening, for example, the adhesive resin layer (B) and the release resin layer (C) after repeated opening and resealing a total of 5 times only by pressure pressing with hands or fingers. The delamination strength (reseal peel strength) is preferably 0.5 N / 15 mm width or more. Here, the reseal peel strength is 0.5 N / 15 mm width or more, preferably 0.75 N / 15 mm width or more, more preferably 1.0 N / 15 mm width or more (only re-seal strength is obtained by pressure bonding with hands or fingers). The upper limit of the sealing peel strength is not more than the delamination strength between the adhesive resin layer (B) and the release resin layer (C), preferably not more than 10 N / 15 mm width, more preferably not more than 5.0 N / 15 mm width. If so, it is preferable because practical resealability can be obtained.

  In the present invention, as a preferable combination of the surface resin layer (A), the adhesive resin layer (B), the release resin layer (C), and the heat seal resin layer (D) satisfying such a condition, as described above, the surface The resin layer (A) is mainly composed of at least one thermoplastic resin selected from the group consisting of an olefin resin, an amide resin, a saponified ethylene-vinyl acetate copolymer, an ester resin, and a styrene resin. A layer composed of a thermoplastic elastomer and a tackifier as a main component is disposed as an adhesive resin layer (B), and an ester resin or an amide resin is used as a release resin layer (C). And a layer composed mainly of an olefin resin as the heat seal resin layer (D).

Next, the thickness of each layer described above will be described.
The surface resin layer (A) is a resin layer having a single layer or a multilayer structure, and usually has a thickness of 1 μm or more, preferably 10 μm or more, more preferably 20 μm or more, and 1000 μm or less, preferably 600 μm or less, Preferably it is 500 micrometers or less. Here, if the thickness of the surface resin layer (A) is 1 μm or more, it is easy to dispose a layer imparting characteristics such as gas barrier properties and pinhole resistance and an adhesive resin layer, and the thickness thereof. If it is 1000 μm or less, heat is easily transferred to the bottom material of the present invention at the time of deep drawing, so that deep drawing can be easily performed.

  The adhesive resin layer (B) is usually a resin layer having a single layer structure, and the thickness thereof is not particularly limited, but the balance between easy-openability and resealability, moldability, production cost, etc. Therefore, 0.5 μm or more, preferably 5 μm or more, more preferably 10 μm or more and 100 μm or less, preferably 70 μm or less, more preferably 50 μm or less is suitably employed.

  The total thickness of the release resin layer (C) and the heat seal resin layer (D) is not particularly limited, but is 1 μm or more, preferably 3 μm or more, more preferably 5 μm or more, 30 μm or less, preferably 25 μm. In the following, it is more preferable that the thickness is 15 μm or less. Here, if the total thickness is 1 μm or more, it is preferable because the deformation such as pressurization by a heat seal hot plate at the time of heat sealing can prevent problems such as deterioration of the function of each layer, and the thickness is also preferable. If it is 30 μm or less, the release resin layer (C) and the heat seal resin layer (D) can be easily broken when the adhesive resin layer (B) and the release resin layer (C) are peeled off. It is preferable because the layer (B) can be exposed in a resealable state.

  For the same reason, an adhesive resin layer (E) composed mainly of an olefin adhesive resin and / or a styrene thermoplastic elastomer between the release resin layer (C) and the heat seal resin layer (D). Even in the case of arranging, the total thickness is 1 μm or more, preferably 3 μm or more, more preferably 5 μm or more, 30 μm or less, preferably 25 μm or less, more preferably 15 μm or less.

  The thickness of the release resin layer (C) is 0.5 μm or more, preferably 1 μm or more, more preferably 1.5 μm or more and 29.5 μm or less, preferably 20 μm or less, more preferably 10 μm or less. If the thickness of the release resin layer (C) is 0.5 μm or more, the release resin layer (C) is deformed by the heat sealing pressure during heat sealing, and there are few problems such as a decrease in the function as the release resin layer. If the thickness is 29.5 μm or less, even when a resin having high rigidity such as an ester resin is disposed on the release resin layer (C), it is easily broken at the time of opening and the film remains. This is preferable because it is difficult for problems such as these to occur.

Next, the manufacturing method of the bottom material of this invention is demonstrated.
Although it does not restrict | limit especially as a manufacturing method of the bottom material of this invention, The coextrusion method excellent in protection, productivity, hygiene, etc. of an adhesive resin layer (B) can be used suitably. That is, the resin compositions used for the surface resin layer (A), the adhesive resin layer (B), the release resin layer (C), and the heat seal resin layer (D) described above are heated and melted in separate extruders, After being laminated in the order of (A) / (B) / (C) / (D) in a molten state by a known method such as a multi-manifold method or a feed block method, a multilayer film is formed by a T-die / chill roll method or an inflation method. Can be molded. Here, in order to improve printing suitability and laminate suitability, it is preferable to perform a surface treatment on the surface of the outermost layer of the surface resin layer (A) of the obtained multilayer film. Examples of the surface treatment include corona treatment, plasma treatment, chromic acid treatment, flame treatment, surface oxidation treatment such as hot air treatment ozone / ultraviolet treatment, and surface unevenness treatment such as sand blasting. Corona treatment is preferably used from the viewpoint of treatment effect, productivity, and manufacturing cost.

  The bottom material of the present invention, on the surface resin layer (A) opposite to the surface on which the adhesive resin layer (B) is laminated, by a known method such as a dry lamination method or an extrusion lamination method, if necessary, A laminate base material can be laminated through an adhesive resin, an adhesive, or the like to obtain a laminate film or laminate sheet. Here, the laminate base material is not particularly limited, and examples thereof include an unstretched polypropylene film, an unstretched polyethylene terephthalate sheet, an unstretched polyethylene film, paper, and a nonwoven fabric. In the present invention, a dry lamination method is preferably used, and examples of the adhesive used at that time include a polyester-polyurethane adhesive and a polyether-polyurethane adhesive.

[Packaging]
The bottom material itself of the present invention, or the laminate film or laminate sheet obtained by laminating the bottom material of the present invention and a laminate base material can be used as the bottom material of various packaging bodies.
For example, when the laminate film is deep-drawn and used as the bottom material of a package (container), the heat seal resin layer (D) of the bottom material and the heat seal resin layer of the lid material (sealed body) Can be made into a package (container) having airtightness, practical initial peel strength, and resealing function. This package (container) is exposed on the peeled surface after opening in a state where the adhesive resin layer (B) can be resealed, and can be resealed only by pressure pressing with a hand or a finger.

Next, the reseal function in the deep drawn package using the bottom material of the present invention will be described.
FIG. 1 is a partial cross-sectional view of a deep-drawn package using the bottom material of the present invention, and FIG. 2 is a state in which a part of the bottom material is peeled off from a lid material in the deep-drawn package shown in FIG. FIG. 3 is a partial cross-sectional view of the package, and FIG. 3 is a partial cross-sectional view showing a state in which the bottom material and the lid material are resealed in the deep-drawn package shown in FIG.

  1 to 3, reference numeral 1 is a bottom material, reference numeral 2 is a lid member (sealed body), reference numeral 3 is a surface resin layer of the bottom material, reference numeral 4 is an adhesive resin layer of the bottom material, and reference numeral 5 is a bottom. Peeling resin layer of material, 6 is a heat seal resin layer of the bottom material, 7 is a surface resin layer of the cover material, 8 is a heat seal resin layer of the cover material, 9 is a heat seal portion, 10 is a tab portion Reference numeral 11 denotes an exposed portion of the adhesive resin layer 4 at the time of peeling, and reference numeral 12 denotes an exposed portion of the peeling resin layer 5 at the time of peeling.

  When the bottom material of the present invention is used in a deep drawn package, as shown in FIG. 1, the bottom material 1 is composed of a surface resin layer 3, an adhesive resin layer 4, a release resin layer 5, and a heat seal resin layer 6 in this order. Consists of. The heat seal resin layer 6 of the bottom material 1 is heat-sealed with the heat seal resin layer 8 of the lid member 2 which is a sealed object. That is, the bottom material 1 and the lid material 2 are bonded together by the heat seal portion 9 formed by heat sealing.

  When the tab portion 10 provided on the lid member 2 is picked and pulled, as shown in FIG. 2, in the heat seal portion 9, first, the release resin layer 5 and the heat seal resin layer 6 on the tab portion 10 side are removed from the bottom material 1. While being ruptured, peeling is started between the adhesive resin layer 4 and the release resin layer 5 in the bottom material 1. When peeling between the adhesive resin layer 4 and the release resin layer 5 reaches the heat seal portion 9 on the side opposite to the tab portion 10 side, the release resin layer 5 and the heat seal resin layer 6 of the bottom material 1 are broken. The release resin layer 5 and the heat seal resin layer 6 of the bottom material 1 that have been broken move to the cover material 2 side that is the sheet body, and the exposed portion 11 of the adhesive resin layer 4 and the exposed portion 12 of the release resin layer 5 It is formed.

  In the case of resealing, as shown in FIG. 3, the peeled cover material 2 is placed on the bottom material 1, and the surface resin layer 3 is pressure-bonded by hand or fingers to form the adhesive resin layer 4 of the bottom material 1. By overlapping the exposed portion 11 and the exposed portion 12 of the release resin layer 5 of the bottom material 1 that has moved to the lid material 2, the bottom material 1 and the lid material 2 can be resealed.

  The bottom material of the present invention can be used as a bottom material for various containers, and its use is not particularly limited. For example, instant noodles, snack confectionery, chocolate confectionery, processed meat products such as sliced ham, wet tissue, etc. Such as cosmetics, sanitary products, shipping medicines, emergency adhesive plasters, throat candy, etc., used as the bottom material of containers packaged in units of several pieces, such as sweat paper, perfume, disposable diapers, etc. Can be used as a bottom material of a packaged container. In particular, it can be suitably used as a package for storing contents that remain susceptible to deterioration such as oxidative deterioration, moisture absorption, and drying after the opening.

The present invention will be described in more detail with reference to the following examples. However, the present invention is not limited to these examples.
In addition, the various measured values and evaluation about the film displayed in this specification were performed as follows. Here, the flow direction from the extruder of the film is called the vertical direction, and the orthogonal direction is called the horizontal direction.

(1) Initial peeling strength The bottom material of the obtained deep-drawn package and the heat seal part of the lid were cut into strips having a width of 15 mm and used as test pieces. When this specimen is pulled at an angle of 180 degrees under the conditions of a temperature of 23 ° C. and a tensile speed of 200 mm / min using a universal testing machine (manufactured by Intesco Corp.), peeling when the bottom material and the lid material are peeled The maximum strength was measured as the initial peel strength (N / 15 mm width).

(2) Membrane remaining situation The situation when peeled by hand from the bottom seal of the obtained deep-drawn package and the heat seal part of the lid was visually evaluated according to the following criteria.
○: When the resin layer breaks cleanly and there is no film residue or fluffing ×: When the resin layer cannot be broken or film breakage or fluffing occurs even when broken

(3) Reseal peel strength After opening again from the heat-sealed part of the resulting deep-drawn package, the lid and bottom material are resealed by pressure and pressure again with a finger, and then the opening and resealing are repeated a total of 5 times The peel strength (reseal peel strength) was measured under the same conditions as (2) initial peel strength. In addition, the following standards are also shown.
○: When the reseal peel strength is 0.5 N / 15 mm width or more ×: When the reseal peel strength is less than 0.5 N / 15 mm width

Example 1
[Bottom material]
The surface resin layer (A) has a three-layer structure using the following three types of resins.
A1: Saponified ethylene-vinyl acetate copolymer (manufactured by Kuraray Co., Ltd., trade name “Eval E105”, hereinafter abbreviated as “EVOH”)
A2: 6-66 nylon resin (Mitsubishi Engineering Plastics Co., Ltd., trade name “Novamid 2030”, hereinafter abbreviated as “6-66Ny”)
A3: Olefin-based adhesive resin (manufactured by Mitsui Chemicals, trade name “Admer NF558”, hereinafter abbreviated as “AD1”)

  The adhesive resin layer (B) is a styrene thermoplastic elastomer (manufactured by Kuraray Co., Ltd., trade name “Septon 2063”, hydrogenated product of styrene-isoprene-styrene, styrene content: 13 mass%, hereinafter abbreviated as “TPS1”. 70 parts by mass and 30 parts by mass of tackifier (Arakawa Chemical Industries, trade name “Arcon P-100”, petroleum hydrocarbon resin, hereinafter abbreviated as “TF1”) A resin composition that was uniformly mixed and pelletized by an extruder was used.

  The release resin layer (C) is an amorphous polyester resin (manufactured by Eastman Chemical Co., Ltd., trade name “EASTAR PETG Copolyester 6763”, hereinafter abbreviated as “PETG”), and the heat seal resin layer (D) is an olefin. Resin composition obtained by mixing 1000 ppm of erucic acid amide as a lubricant and 2000 ppm of natural silica as an anti-blocking agent to a system adhesive resin (manufactured by Mitsui Chemicals, Inc., trade name “Admer SF715”, hereinafter abbreviated as “AD2”) Each was composed.

  (A) Extruder for layer (single screw extruder of 50 mm in diameter for all three layers), (B) Extruder for layer (single screw extruder of 50 mm in diameter), (C) Extruder for layer (caliber) 50 mm single-screw extruder), (D) T-die / chill roll co-extrusion multi-layer film production apparatus having a layer extruder (single-screw extruder with a diameter of 50 mm) is supplied to each extruder and set for extrusion. Co-extruded under the conditions of a temperature of 190 to 230 ° C. and a T die set temperature of 235 ° C., and the average of each layer in a six-layer configuration of (A1) / (A2) / (A3) / (B) / (C) / (D) A multilayer film (X1) having a thickness of 10 μm / 20 μm / 10 μm / 20 μm / 5 μm / 5 μm and a total thickness of 70 μm was obtained.

  Next, an unstretched polyethylene terephthalate sheet (manufactured by Mitsubishi Chemical Corporation, trade name “Novaclear”, thickness 250 μm) is applied to the outermost layer side of the surface resin layer (A) of the obtained multilayer film (X1) by a dry lamination method. By bonding, a laminate film (X1LS) having a total thickness of 320 μm was obtained and used as the bottom material of the package.

  In addition, as an adhesive for dry lamination, a two-component curable adhesive (manufactured by Dainippon Ink Co., Ltd. as the main agent, trade name “Dick Dry LX-75A”, as a curing agent, produced by Dainippon Ink Co., Ltd., trade name “Dick Dry KW-40” was used.

[Cover material]
From the outermost layer side, EVOH, 6-66Ny, AD1, linear low density polyethylene resin (manufactured by Nippon Polyethylene Co., Ltd., trade name “NOVATEC LL UF240”, hereinafter abbreviated as “LLDPE”) as erucic acid amide as a lubricant Is laminated in the order of a resin composition (heat seal resin layer) in which 1000 ppm of natural silica is added and mixed as an antiblocking agent, and the average thickness of each layer is 10 μm / 20 μm / 10 μm / 30 μm, respectively, and the total thickness is 70 μm. A multilayer film (Y1) was obtained by coextrusion. A biaxially stretched polyethylene terephthalate film base material (product name “Embret PET” manufactured by Unitika Ltd.) with a total thickness of 16 μm is pasted on the outermost layer side (EVOH surface) of this multilayer film (Y1) by a dry lamination method. In addition, a laminate sheet (Y1LF) having a total thickness of 86 μm was obtained and used as a lid for the package.
In addition, the grade similar to the case where a laminate film (X1LS) is produced was used as an adhesive for dry lamination.

[Deep-drawn packaging]
Using a deep-drawing packaging machine (manufactured by Mulchback Co., Ltd., model number: R-530), the bottom material (X1LS) is deep-drawn so that the unstretched polyethylene terephthalate sheet layer becomes the outer layer, thereby a length of 130 mm. The container is processed into a rectangular container having a width of 170 mm and a flange width of 6 mm. In the heat seal portion, the above-mentioned lid material (Y1LF) is applied to the flange portion provided on the deeply drawn bottom material. A deep-drawn package was produced by heat sealing under the conditions of ° C., sealing time: 2 seconds, sealing pressure: 4 kg / cm ² .
The results of evaluation using this deep-drawn package are shown in Table 1.

(Example 2)
[Bottom material]
In Example 1, the resin used for the adhesive resin layer (B) was 45 parts by mass of TPS1 used in Example 1 and a styrene-based thermoplastic elastomer (manufactured by JSR Corporation, trade name “Dynalon 1320P”, styrene-butadiene. Random copolymer hydrogenated product, styrene content: 10% by mass, hereinafter abbreviated as “TPS2”) 25 parts by mass and tackifier (trade name “YS Resin PX1150” manufactured by Yasuhara Chemical Co., Ltd.), terpene resin Hereinafter, it is abbreviated as “TF2”.) (A1) / (A2) in the same manner as in Example 1 except that 30 parts by mass was changed to a resin composition obtained by uniformly mixing and pelletizing with a twin-screw extruder. / (A3) / (B) / (C) / (D), each layer has an average thickness of 10 μm / 20 μm / 10 μm / 20 μm / 5 μm / 5 μm and a total thickness of 70 μm It was obtained Irumu (X2). Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X2LS) having a total thickness of 320 μm, which was used as the bottom material of the package.

[Cover material]
In the same manner as in Example 1, a laminate sheet (Y1LF) was used for the lid of the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

(Example 3)
[Bottom material]
The surface resin layer (A) has a two-layer structure using the following two types of resins.
A1: EVOH
A2: AD1

  The adhesive resin layer (B) was configured using a mixed resin composition of TPS1 and TF1 as in Example 1.

  The release resin layer (C) was formed using PETG as in Example 1.

  The heat seal resin layer (D) was made of LLDPE and mixed with 1000 ppm of erucamide as a lubricant and 2000 ppm of natural silica as an antiblocking agent, and the adhesive resin layer (E) was made of AD2.

  (A) Extruder for layer (single-screw extruder with a diameter of 50 mm for both layers), (B) Extruder for layer (single-screw extruder with a diameter of 50 mm), (C) Extruder for layer (caliber) 50 mm single-screw extruder) and (D) each extruder of a T-die / chill roll co-extrusion multilayer film production apparatus having a layer extruder (both layers have a diameter of 50 mm). , Extrusion extrusion temperature 190-230 ° C, T die set temperature 235 ° C co-extrusion, (A1) / (A2) / (B) / (C) / (E) / (D) A multilayer film (X3) having an average thickness of each layer of 15 μm / 22 μm / 20 μm / 5 μm / 3 μm / 5 μm and a total thickness of 70 μm was obtained. Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X3LS) having a total thickness of 320 μm, which was used as the bottom material of the package.

[Cover material]
In the same manner as in Example 1, a laminate sheet (Y1LF) was used for the lid of the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

Example 4
[Bottom material]
In Example 1, the resin used for the release resin layer (C) is an amorphous polyamide resin (product name “Novamid X21” manufactured by Mitsubishi Engineering Plastics Co., Ltd., hereinafter abbreviated as “amorphous Ny”). ), Except that the resin used in the heat seal resin layer (D) was changed to a resin composition in which AD1 was mixed with 1000 ppm of erucic acid amide as a lubricant and 2000 ppm of natural silica as an antiblocking agent. The average thickness of each layer is 10 μm / 20 μm / 10 μm / 20 μm / 5 μm / 5 μm in a six-layer configuration of (A1) / (A2) / (A3) / (B) / (C) / (D). A multilayer film (X4) having a total thickness of 70 μm was obtained. Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X4LS) having a total thickness of 320 μm, which was used as the bottom material of the package.

[Cover material]
In the same manner as in Example 1, a laminate sheet (Y1LF) was used for the lid of the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

(Example 5)
[Bottom material]
In Example 3, except that the resin used for the release resin layer (C) is amorphous Ny and the resin used for the adhesive resin layer (E) is changed to AD1, (Example 3) ( A1) / (A2) / (B) / (C) / (E) / (D), the average thickness of each layer is 15 μm / 22 μm / 20 μm / 5 μm / 3 μm / 5 μm, respectively. A multilayer film (X5) having a thickness of 70 μm was obtained. Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X5LS) having a total thickness of 320 μm, which was used as the bottom material of the package.

[Cover material]
In the same manner as in Example 1, a laminate sheet (Y1LF) was used for the lid of the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

(Example 6)
[Bottom material]
In Example 4, the resin used for the heat seal resin layer (D) is an olefin (PP) adhesive resin (product name “QF551”, hereinafter abbreviated as “AD3”, manufactured by Mitsui Chemicals, Inc.). (A1) / (A2) / (A3) / (B In the same manner as in Example 1, except that the resin composition was mixed with 1000 ppm of erucic acid amide as a lubricant and 2000 ppm of natural silica as an antiblocking agent. ) / (C) / (D), a multilayer film (X6) having an average thickness of 10 μm / 20 μm / 10 μm / 20 μm / 5 μm / 5 μm and a total thickness of 70 μm was obtained. . Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X6LS) having a total thickness of 320 μm, which was used as the bottom material of the package.

[Cover material]
From the outermost layer side, EVOH, 6-66Ny, AD3, polypropylene resin (manufactured by Nippon Polypro Co., Ltd., trade name “NOVATEC PP EG6D”, hereinafter abbreviated as “PP”), 1000 ppm of erucamide as a lubricant, anti A resin composition (heat seal resin layer) in which 2000 ppm of natural silica was added and mixed as a blocking agent was laminated in this order, and each layer had an average thickness of 10 μm / 20 μm / 10 μm / 30 μm and a multilayer film having a total thickness of 70 μm ( Y2) was obtained by coextrusion method. A biaxially stretched polyethylene terephthalate film base material (product name “Embret PET” manufactured by Unitika Ltd.) with a total thickness of 16 μm is pasted on the outermost layer side (EVOH surface) of this multilayer film (Y2) by the dry lamination method. In addition, a laminate sheet (Y2LF) having a total thickness of 86 μm was obtained and used as a lid for the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

(Comparative Example 1)
[Bottom material]
In Example 1, the release resin layer (C) was not disposed, and the average thickness of each layer was 10 μm / each with a five-layer configuration of (A1) / (A2) / (A3) / (B) / (D). A multilayer film (X7) having a total thickness of 65 μm was obtained in the same manner as in Example 1 except that the thickness was changed to 20 μm / 10 μm / 20 μm / 5 μm. Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X7LS) having a total thickness of 320 μm and used as the bottom material of the package.

[Cover material]
In the same manner as in Example 1, a laminate sheet (Y1LF) was used for the lid of the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

(Comparative Example 2)
[Bottom material]
In Example 6, the release resin layer (C) was not disposed, and the average thickness of each layer was 10 μm / each in a five-layer configuration of (A1) / (A2) / (A3) / (B) / (D). A multilayer film (X8) having a total thickness of 65 μm was obtained in the same manner as in Example 6 except that the thickness was changed to 20 μm / 10 μm / 20 μm / 5 μm. Next, in the same manner as in Example 6, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X8LS) having a total thickness of 320 μm, which was used as the bottom material of the package.

[Cover material]
In the same manner as in Example 6, a laminate sheet (Y2LF) was used as a lid for the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

(Reference example)
[Bottom material]
In Example 1, in a six-layer configuration of (A1) / (A2) / (A3) / (B) / (C) / (D), only the thickness of the release resin layer (C) was 40 μm, and the average of each layer A multilayer film (X9) having a total thickness of 105 μm was obtained in the same manner as in Example 1 except that the thickness was changed to 10 μm / 20 μm / 10 μm / 20 μm / 40 μm / 5 μm, respectively. Next, in the same manner as in Example 1, unstretched polyethylene terephthalate sheets were bonded together by a dry lamination method to obtain a laminate film (X9LS) having a total thickness of 355 μm, which was used as the bottom material of the package.

[Cover material]
In the same manner as in Example 1, a laminate sheet (Y1LF) was used for the lid of the package.

[Deep-drawn packaging]
A deep-drawn package was produced in the same manner as in Example 1. The results of evaluation using this deep-drawn package are shown in Table 1.

From Table 1, the resealable packaging body (deep-drawing packaging body) formed with the bottom material defined in the present invention has all the characteristics of adhesive resin exposure status, initial peel strength, remaining film status, and reseal peel strength. It was confirmed that this was practical and practical (Examples 1 to 6). Moreover, in this invention, it has favorable easy openability and resealability irrespective of the material of a to-be-sealed body (for example, Example 2 and Example 6).
On the other hand, in the case of a package formed of a bottom material made of a film that does not have a release resin layer between the adhesive resin layer and the heat seal resin layer, the initial peel strength is too high, so it can be easily opened by hand. It was difficult to do, and the reseal peel strength was also insufficient (Comparative Examples 1-2).
In addition, when the total thickness of the adhesive resin layer and the heat seal resin layer becomes thick (when it exceeds 30 μm), the peel resin layer and the heat seal resin layer cannot be broken when peeled by hand from the heat seal portion, and the film remains. There was a tendency to occur (reference example).

  Since the present invention has both good easy-openability and good resealability only by pressure and pressure bonding with hands and fingers, regardless of the material of the sealed body, it is suitable for packaging bodies such as foods, pharmaceuticals, and cosmetics. It can be widely used as a bottom material.

It is a fragmentary sectional view of the package using the bottom material of the present invention. In the packaging body shown in FIG. 1, it is a fragmentary sectional view of the packaging body of the state which peeled a part of cover material from the container. In the package shown in FIG. 1, it is a fragmentary sectional view which shows the state which resealed the bottom material and the cover material.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Bottom material 2 Cover material 3 Surface resin layer of bottom material 4 Adhesive resin layer of bottom material 5 Peeling resin layer of bottom material 6 Heat seal resin layer of bottom material 7 Surface resin layer of lid material 8 Heat seal resin layer of lid material 9 Heat seal portion of bottom material 10 Tab portion of lid material 11 Exposed portion of adhesive resin layer at peeling 12 Exposed portion of heat seal resin layer at peeling

Claims (9)

The surface resin layer (A), the adhesive resin layer (B), the release resin layer (C) and the heat seal resin layer (D) are laminated in the order of (A) / (B) / (C) / (D), The adhesive resin layer (B) is a styrene thermoplastic elastomer (b1) and a tackifier (b2), the release resin layer (C) is an ester resin , the heat seal resin layer (D) is an olefin resin, and And / or a layer composed mainly of a styrene-based thermoplastic elastomer, the total thickness of the release resin layer (C) and the heat seal resin layer (D) being 1 μm to 30 μm, and the release resin Ri der thickness 0.5μm or 29.5μm following layers (C), used in the base material of the multilayer film characterized by being produced by coextrusion, the heat-sealing resin layer of the multilayer film (D ) When the base material and the cover material are heat sealed by heat sealing to the seal part, and then the cover material is peeled from the heat seal part, in the heat seal part, the adhesive resin layer (B) and the peel The resin layer (C) is delaminated, and the adhesive resin layer (B) is exposed in a state where it can be resealed with the release resin layer (C). B) is exposed in the heat seal portion, the release resin layer (C) and the heat seal resin layer (D) are broken from the bottom material, and the adhesive resin layer (B) and the release resin layer ( A re-sealable packaging body which is formed by delamination with C) and transfer of the release resin layer (C) and the heat seal resin layer (D) to the sealed body side. The surface resin layer (A) mainly comprises at least one thermoplastic resin selected from the group consisting of olefin resins, amide resins, saponified ethylene-vinyl acetate copolymers, ester resins, and styrene resins. The resealable packaging according to claim 1, which is configured as a component. The styrenic thermoplastic elastomer (b1) is a hydrogenated styrene-butadiene block copolymer (SB), a hydrogenated styrene-isoprene block copolymer (SI), or a styrene-butadiene-styrene block copolymer. (SBS) hydrogenated product, styrene-isoprene-styrene block copolymer (SIS) hydrogenated product, styrene-isoprene-butadiene-styrene block copolymer (SIBS) hydrogenated product, styrene-butadiene random copolymer A hydrogenated product of at least one styrenic thermoplastic elastomer selected from the group consisting of a hydrogenated product of a polymer (SBR) and a hydrogenated product of a styrene-isoprene random copolymer (SIR). Item 3. The resealable package according to item 1 or 2. The tackifier (b2) is at least one tackifier selected from the group consisting of a rosin resin, a terpene resin, and a petroleum hydrocarbon resin. The re-sealable package described in 1. The resealable packaging body according to claim 4, wherein the content of the tackifier (b2) in the adhesive resin layer (B) is 2 mass% or more and 50 mass% or less. The surface resin layer (A) is composed of two or more layers, and has a layer mainly composed of a saponified ethylene-vinyl acetate copolymer and / or a layer mainly composed of an amide resin. Item 6. The resealable package according to any one of Items 1 to 5. An adhesive resin layer (E) composed mainly of an olefin-based adhesive resin and / or a styrene-based thermoplastic elastomer-based adhesive resin between the release resin layer (C) and the heat seal resin layer (D). The re-sealable packaging body according to any one of claims 1 to 6, further comprising: The resealable material according to claim 7, wherein a total thickness of the release resin layer (C), the adhesive resin layer (E), and the heat seal resin layer (D) is 1 µm or more and 30 µm or less. Packaging. The ester resin constituting the release resin layer (C) is a polyethylene terephthalate resin, and is low crystalline or amorphous containing 1,4-cyclohexanedimethanol units in a total glycol monomer unit of 15 mol% to 50 mol%. The resealable packaging body according to any one of claims 1 to 8, which is at least one ester resin selected from a group consisting of a conductive polyethylene terephthalate resin.

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