JP5698503B2 - Self-supporting bags and methods for reducing the volume of self-supporting bags - Google Patents

Description

  The present invention relates to a self-supporting bag and a method for reducing the volume of a self-supporting bag.

  Conventionally, a bag formed by heat-sealing a laminated film has been widely used as an inexpensive packaging container for easily sealing and packaging the contents and distributing and storing them. Such a laminated film bag is provided with various physical properties by selecting a constituent material of the laminated film. Examples of physical properties to be imparted include processability, sealing properties, moisture resistance, gas barrier properties, water resistance, heat resistance, content resistance properties, suitability for retort treatment, and suitability for heating in a microwave oven.

  As described above, desired physical properties can be easily imparted to a bag formed by heat-sealing a laminated film (a sealant layer, a base material layer, etc.). For this reason, bags formed by heat-sealing laminated films are used in a wide range of fields including various foods as well as non-foods. Specifically, it is used by processing into a three-sided seal type, four-sided seal type, pillow type, etc. flat bag, a gusset bag, a standing pouch, or a modified or applied type bag.

  Among these, the standing pouch type and the like self-supporting bags have the characteristics of a three-dimensional container as well as the self-supporting properties, and are easy to handle and can be packaged compactly for the capacity. A self-supporting bag such as a standing pouch can be folded when the contents are not included in the bag. For this reason, when transporting only the bag before filling the contents, the volume can be reduced when discarding after use. As a result, a standing pouch type or the like is generally used as a bag that is filled with contents having fluidity such as liquid, powder or granular.

Such a self-supporting bag is likely to be difficult to open for reasons such as high heat seal strength. Therefore, in order to impart an easy cutting property to the self-supporting bag, an intermediate layer provided between the sealant layer and the substrate layer, the inclusion of O olefin-based resin in the intermediate layer (Patent Document 1).

JP 09-141791 A

  By the way, a general self-supporting bag including the self-supporting bag described in Patent Document 1 has a problem of the three-dimensional shape stability of the self-supporting bag such as a crushed waist.

  In addition, as described above, the self-supporting bag can be folded and transported before transporting the contents, and is easily transported. However, if the self-supporting bag can be reduced in volume, its transportation becomes easier.

  The present invention has been made in order to solve the above-mentioned problems, and its purpose is to make the above-mentioned problem of stability of the three-dimensional shape difficult to occur due to crushed of the bag itself, and to reduce the volume of the self-supporting bag. There is.

  The inventors of the present invention have made extensive studies to solve the above problems. As a result, the present inventors have found that the above problem can be solved when the sealant layer is composed of a thermoplastic resin film containing a cyclic olefin-based resin and a linear low-density polyethylene, thereby completing the present invention. More specifically, the present invention provides the following.

  (1) Self-supporting property comprising: a base material layer composed of a biaxially stretched nylon film; and a sealant layer composed of a thermoplastic resin film having a layer containing a cyclic olefin-based resin and a linear low-density polyethylene. bag.

  (2) The said thermoplastic resin film is a self-supporting bag as described in (1) which contains 10 to 40 mass% of cyclic olefin resin.

  (3) The self-supporting bag according to (1) or (2), wherein the cyclic olefin-based resin is a copolymer of ethylene and norbornene.

  (4) The said cyclic olefin resin is a self-supporting bag as described in (3) whose glass transition point is 60 degreeC or more and 90 degrees C or less.

  (5) A method for reducing the volume of a self-supporting bag having a sealant layer containing linear low-density polyethylene, wherein the sealant layer has a layer containing a cyclic olefin-based resin. .

  According to the present invention, in the state where the contents are contained in the self-supporting bag, the problem due to the crushing of the bag itself hardly occurs, and further, the volume of the self-supporting bag can be reduced.

(A) is a perspective view which shows typically an example of the self-supporting bag of this invention. FIG. 2B is a schematic diagram of an AA cross section in FIG. (A) is a figure which shows the measurement result of the water vapor permeability of evaluation 1. (B) is a figure which shows the measurement result of the haze value of evaluation 2. FIG. It is a figure which shows the measurement result of the heat seal intensity | strength of the evaluation 3. It is a figure which shows the measurement result of the heat seal intensity | strength of the evaluation 4.

  Hereinafter, embodiments of the present invention will be described in detail. In addition, this invention is not limited to the following embodiment.

<Independent bag>
The self-supporting bag of the present invention is a sealant layer composed of a thermoplastic resin film having a base layer composed of a biaxially stretched nylon film, and a layer containing a cyclic olefin-based resin layer and a linear low-density polyethylene. And comprising. The self-supporting bag of the present invention will be described using a standing pouch as an example.

  Fig.1 (a) is a perspective view which shows typically an example of the self-supporting bag of this invention. FIG.1 (b) is a schematic diagram of the AA cross section of FIG. As shown in FIG. 1B, the self-supporting bag 1 of the present invention includes a base material layer 10 and a sealant layer 11.

[Base material layer]
The base material layer 10 is composed of a biaxially stretched nylon film. As the biaxially stretched nylon film, a general one (for example, a nylon 6 film) can be used. The biaxially stretched nylon film may be produced by a conventionally known method, or a commercially available product may be used. Commercially available products include, for example, Idemitsu Petrochemical Co., Ltd. Unilon, Unitika Co., Ltd. emblem, Kojin Co., Ltd. Bonaire, Toyobo Co., Ltd. Baden, Mitsubishi Kasei Polytech Co., Ltd. Santo Neil, etc. The ones sold at

  Moreover, the film of the blend material of other nylon or 2 or more types of nylon may be sufficient. For example, Idemitsu Petrochemical Co., Ltd. Uniathlon film, which is a blend film of nylon 6 and special nylon, can be mentioned.

  Further, depending on the purpose, the film surface of the biaxially stretched nylon film may be coated with polyvinylidene chloride, or silicon oxide, alumina or the like may be evaporated.

  The biaxially stretched nylon film may contain components other than nylon as long as the effects of the present invention are not impaired.

  Although the thickness of the base material layer 10 is not specifically limited, For example, it is preferable that they are 10 micrometers or more and 30 micrometers or less. A biaxially stretched nylon film having the above thickness is used depending on the shape and application of the self-supporting bag.

[Sealant layer]
The sealant layer 11 is composed of a thermoplastic resin film, and the thermoplastic resin film has a layer (hereinafter sometimes referred to as “blend layer”) containing a cyclic olefin-based resin and a linear low-density polyethylene. First, cyclic olefin resin and linear low density polyethylene are demonstrated.

  The cyclic olefin resin is not particularly limited as long as it contains a cyclic olefin component as a copolymerization component and is a polyolefin resin containing the cyclic olefin component in the main chain. For example, an addition polymer of a cyclic olefin or a hydrogenated product thereof, an addition copolymer of a cyclic olefin and an α-olefin, or a hydrogenated product thereof can be used.

  The cyclic olefin-based resin includes those obtained by grafting and / or copolymerizing an unsaturated compound having a polar group to the above polymer.

  Examples of the polar group include a carboxyl group, an acid anhydride group, an epoxy group, an amide group, an ester group, and a hydroxyl group. Examples of the unsaturated compound having a polar group include (meth) acrylic acid and maleic acid. Acid, maleic anhydride, itaconic anhydride, glycidyl (meth) acrylate, alkyl (meth) acrylate (carbon number 1-10) ester, maleic acid alkyl (carbon number 1-10) ester, (meth) acrylamide, (meta ) 2-hydroxyethyl acrylate.

  The cyclic olefin resin is preferably an addition copolymer of a cyclic olefin and an α-olefin or a hydrogenated product thereof.

  Moreover, as the cyclic olefin-based resin containing the cyclic olefin component used in the present invention as a copolymerization component, a commercially available resin can be used. Examples of commercially available cyclic olefin-based resins include TOPAS (registered trademark) (Topas Advanced Polymers), Apel (registered trademark) (manufactured by Mitsui Chemicals), Zeonex (registered trademark) (manufactured by Nippon Zeon), Examples include ZEONOR (registered trademark) (manufactured by ZEON Corporation), ARTON (registered trademark) (manufactured by JSR Corporation), and the like.

（式中、Ｒ^１〜Ｒ^１２は、それぞれ同一でも異なっていてもよく、水素原子、ハロゲン原子、及び、炭化水素基からなる群より選ばれるものであり、
Ｒ^９とＲ^１０、Ｒ^１１とＲ^１２は、一体化して２価の炭化水素基を形成してもよく、
Ｒ^９又はＲ^１０と、Ｒ^１１又はＲ^１２とは、互いに環を形成していてもよい。
また、ｎは、０又は正の整数を示し、
ｎが２以上の場合には、Ｒ^５〜Ｒ^８は、それぞれの繰り返し単位の中で、それぞれ同一でも異なっていてもよい。） Particularly preferred examples of the addition copolymer of cyclic olefin and α-olefin include: [1] an α-olefin component having 2 to 20 carbon atoms, and [2] a cyclic olefin component represented by the following general formula (I): Can be mentioned.

(Wherein R ^{1 to} R ¹² may be the same as or different from each other, and are selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbon group;
R ⁹ and R ¹⁰ , R ¹¹ and R ¹² may be integrated to form a divalent hydrocarbon group,
R ⁹ or R ¹⁰ and R ¹¹ or R ¹² may form a ring with each other.
N represents 0 or a positive integer;
When n is 2 or more, R ^{5 to} R ⁸ may be the same or different in each repeating unit. )

[[1] α-olefin component having 2 to 20 carbon atoms]
The α-olefin having 2 to 20 carbon atoms is not particularly limited. For example, the thing similar to Unexamined-Japanese-Patent No. 2007-302722 can be mentioned. These α-olefin components may be used alone or in combination of two or more. Of these, ethylene is most preferably used alone.

[[2] Cyclic olefin component represented by formula (I)]
The cyclic olefin component represented by the general formula (I) will be described.

R ^{1 to} R ¹² in the general formula (I) may be the same or different and are selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbon group.

Specific examples of R ^{1 to} R ⁸ include, for example, a hydrogen atom; a halogen atom such as fluorine, chlorine and bromine; a lower alkyl group such as a methyl group, an ethyl group, a propyl group and a butyl group. May be different from each other, may be partially different, or all may be the same.

Specific examples of R ^{9 to} R ¹² include, for example, hydrogen atom; halogen atom such as fluorine, chlorine, bromine; methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, hexyl group, stearyl. Alkyl group such as cyclohexyl group; cycloalkyl group such as cyclohexyl group; substituted or unsubstituted aromatic hydrocarbon group such as phenyl group, tolyl group, ethylphenyl group, isopropylphenyl group, naphthyl group, anthryl group; benzyl group, phenethyl And an aralkyl group in which an aryl group is substituted with an alkyl group, and the like. These may be different from each other, may be partially different, or all may be the same.

Specific examples of the case where R ⁹ and R ¹⁰ or R ¹¹ and R ¹² are integrated to form a divalent hydrocarbon group include, for example, alkylidene groups such as an ethylidene group, a propylidene group, and an isopropylidene group. Can be mentioned.

When R ⁹ or R ¹⁰ and R ¹¹ or R ¹² form a ring with each other, the formed ring may be monocyclic or polycyclic, or may be a polycyclic ring having a bridge. , A ring having a double bond, or a ring composed of a combination of these rings may be used. Moreover, these rings may have a substituent such as a methyl group.

  Specific examples of the cyclic olefin component represented by the general formula (I) include those similar to those described in JP-A-2007-302722.

  These cyclic olefin components may be used singly or in combination of two or more. Among these, it is preferable to use bicyclo [2.2.1] hept-2-ene (common name: norbornene) alone. In particular, if a copolymer of norbornene and ethylene is used as the cyclic olefin-based resin, it is preferable because the problem of crushed back hardly occurs.

  [1] A method for polymerizing an α-olefin component having 2 to 20 carbon atoms and a [2] cyclic olefin component represented by formula (I) and a method for hydrogenating the obtained polymer are particularly limited. Instead, it can be carried out according to known methods. Random copolymerization or block copolymerization may be used, but random copolymerization is preferred.

  The polymerization catalyst used is not particularly limited, and a cyclic olefin resin (B) is obtained by a known method using a conventionally known catalyst such as a Ziegler-Natta, metathesis, or metallocene catalyst. Can do.

[Other copolymer components]
The cyclic olefin-based resin (A) does not impair the object of the present invention other than [1] the α-olefin component having 2 to 20 carbon atoms and [2] the cyclic olefin component represented by the general formula (I). In the range, other copolymerizable unsaturated monomer components may be contained as required.

  The unsaturated monomer that may be optionally copolymerized is not particularly limited, and examples thereof include hydrocarbon monomers containing two or more carbon-carbon double bonds in one molecule. Can be mentioned. Specific examples of the hydrocarbon-based monomer having two or more carbon-carbon double bonds in one molecule include those similar to those described in JP-A-2007-302722.

  The glass transition point of the cyclic olefin resin is preferably 60 ° C. or higher and 90 ° C. or lower. If the glass transition point of cyclic olefin resin is 60 degreeC or more, it is preferable for the reason of maintaining a characteristic at normal use temperature. A glass transition point of 90 ° C. or lower is preferable because it can be sealed within a sealing temperature range of a general sealant. The glass transition point of the cyclic olefin resin can be adjusted by adjusting the content of the cyclic olefin skeleton of the main chain. Moreover, the glass transition point (Tg) employ | adopts the value measured on temperature rising rate 10 degree-C / min conditions by DSC method (method of JISK7121 description).

  The content of the cyclic olefin-based resin contained in the thermoplastic resin film is preferably 10% by mass or more and 40% by mass or less. If it is 10% by mass or more, a significant improvement in elastic modulus is seen, which is preferable because it improves self-sustainability, and if it is 40% by mass or less, a flexible sealant having the characteristics of a polyolefin containing no cyclic olefin is obtained. It is preferable because it can be manufactured.

  Next, the linear low density polyethylene will be described. In the present invention, by combining the cyclic olefin resin and the linear low-density polyethylene, it becomes a self-supporting bag that does not cause problems such as crushed even if the volume is reduced. For example, if low-density polyethylene is used instead of linear low-density polyethylene, the heat sealability is remarkably lowered, and a self-supporting bag is not obtained.

The linear low density polyethylene resin used in the present invention is a copolymer of an α-olefin having 3 or more carbon atoms and ethylene, for example, having a density of about 0.890 to 0.945 g / cm ^3. Point to. The carbon number of the α-olefin as the copolymer component is generally about 3 to 20. Specific examples include propylene, butene-1, methylpentene-1, hexene-1, and octene-1.

The density of the linear low density polyethylene resin is approximately within the above range, but in the present invention, the linear low density polyethylene resin having a density of about 0.90 g / cm ³ or more and 0.94 g / cm ³ or less. Is preferably used. If the density of the linear low density polyethylene resin is 0.90 g / cm ³ or more, it is preferable because it has an appropriate elastic modulus required for a self-supporting bag containing a cyclic olefin, and the density is 0.94 g / cm 3. If it is ³ or less, it is preferable because it has moderate flexibility and transparency as a bag.

  As linear low density polyethylene resin, what was manufactured with the conventionally well-known general manufacturing method using a conventionally well-known general catalyst can be used. Examples of conventionally known catalysts include Ziegler catalysts, metallocene catalysts, vanadium catalysts, and the like. Examples of conventionally known production methods include production methods such as a gas phase polymerization method, a solution polymerization method, a slurry polymerization method, and a high-pressure ion polymerization method. In this invention, it is preferable to use the same kind of catalyst as the catalyst used for manufacture of cyclic olefin resin as mentioned later.

  The content of the linear low density polyethylene in the thermoplastic resin film is preferably 60% by mass or more and 90% by mass or less. If it is 60% by mass or more, polyethylene is preferable because it forms a matrix to form a flexible self-supporting bag, and if it is 90% by mass or less, it is preferable because it exhibits effective self-supporting properties.

  Next, the thermoplastic resin film will be described. The thermoplastic resin film has a layer (blend layer) containing the above cyclic olefin-based resin and linear low-density polyethylene. As described above, by using a thermoplastic resin film having a blend layer formed by molding a blend material of a cyclic olefin-based resin and a linear low-density polyethylene, the problem of shape instability due to crumble is less likely to occur. For example, even if a sealant layer having a cyclic olefin-based resin layer and a linear low-density polyethylene resin layer is used, the three-dimensional shape cannot be sufficiently stabilized.

  In the present invention, as long as it includes a blend layer, it may be a single layer or a multilayer. The thermoplastic resin film may have other layers such as a linear low-density polyethylene resin layer on the inner side (inside the bag) further than the blend layer. As the other layer, a layer having heat sealing properties such as an ethylene-vinyl acetate copolymer, an ethylene-unsaturated carboxylic acid copolymer, and an ionomer can be used. Moreover, when the other layer is outside the blend layer, various resin layers can be used without considering the heat sealability.

  According to the present invention, as described above, since the three-dimensional shape of the self-supporting bag is easily stabilized, the thickness of the thermoplastic resin film can be made thinner than the conventional one. Conventionally, the use of a 130 μm thermoplastic resin film is common, but according to the present invention, even in the range of less than 130 μm and 95 μm or more, the three-dimensional stability of a self-supporting bag equal to or higher than that of the conventional one can be realized.

  The manufacturing method of a thermoplastic resin film is not specifically limited, For example, it can manufacture by a conventionally well-known extrusion molding method. Moreover, when a thermoplastic resin film is a multilayer, it can manufacture by the conventionally well-known T-die multilayer coextrusion method, for example.

  The blend layer may contain components other than the cyclic olefin resin and the linear low density polyethylene as long as the effects of the present invention are not impaired. The linear low density polyethylene resin layer may also contain other components as long as the effects of the present invention are not impaired.

  Subsequently, the manufacturing method of a self-supporting bag is demonstrated. First, a multilayer film having a base material layer and a sealant layer is manufactured. Although the manufacturing method of a multilayer film is not specifically limited, For example, well-known laminating methods, such as an extrusion coating method, a hot lamination method, a dry lamination method, are applicable.

  The multilayer film may include other layers such as a vapor deposition layer in addition to the base material layer and the sealant layer. A conventionally well-known thing can be applied to another layer in the range which does not impair the effect of this invention.

  Next, a self-supporting bag is manufactured using the multilayer film. The method for producing a self-supporting bag from the multilayer film is not particularly limited, and a conventionally known method can be employed. For example, using a conventional standing pouch bag making machine (which may be a single-row bag making machine or a two-row butting bag making machine), an upper surface film supply device, and an upper gusset portion Heat seal devices and trimming devices such as protrusions, spouts, or extension seals that extend to the front and rear pleats, as well as a slitting device that processes the horizontal cut lines provided on the extension seals Alternatively, bag making can be easily performed by appropriately adding a punching device or the like.

<How to reduce the volume of self-supporting bags>
Finally, a method for reducing the volume of the self-supporting bag of the present invention will be described. The description overlapping with the description of the above self-supporting bag may be omitted as appropriate.

  The method of the present invention can be employed in a self-supporting bag comprising a sealant layer comprising linear low density polyethylene. As described above, the sealant layer has a layer containing a linear low-density polyethylene and a cyclic olefin resin, so that even if the thickness of the sealant layer is reduced, problems such as crushed back hardly occur, and the three-dimensional shape is stable. Become a self-supporting bag.

  As long as the sealant layer is as described above, the other layer (for example, the base material layer) may be made of any kind of film. For example, in addition to the biaxially stretched nylon film, a biaxially stretched polyethylene terephthalate film, an unstretched polypropylene film, or the like can be used for the base material layer.

  EXAMPLES Hereinafter, although an Example is shown and this invention is demonstrated concretely, this invention is not limited to these Examples.

<Material>
Biaxially stretched nylon film: manufactured by Kojin Co., Ltd. (“Bonyl RX”), thickness 15 μm
Cyclic olefin-based resin: copolymer of ethylene and norbornene, manufactured by Topas Advanced Polymers ("TOPAS8007F-500"), glass transition point 78 ° C
Linear low density polyethylene 1 (LLDPE1): “Evolue SP2320” manufactured by Prime Polymer Co., Ltd., density 0.920 g / cm ³
Linear low-density polyethylene 2 (LLDPE2): manufactured by Nippon Polyethylene Co., Ltd., “Kernel KC570S”, density 0.906 g / cm ³
Linear low density polyethylene 3 (LLDPE3): manufactured by Nippon Polyethylene Co., Ltd., “Harmolex NH745N”, density 0.913 g / cm ³
Low density polyethylene (LDPE): “Novatec LC607K” manufactured by Nippon Polyethylene Co., Ltd., density 0.919 g / cm ³ .

<Evaluation 1>
Inflation films (thickness: 100 μm) of the following evaluation 1-1 to evaluation 1-5 were prepared, and based on JIS K7129 (Method A), using a Lyssy L80 series water vapor transmission meter at 40 ° C. and a relative humidity of 90%. The water vapor transmission rate was measured. The measurement results are shown in FIG.
(Evaluation 1-1) Inflation film consisting only of LLDPE1,
(Evaluation 1-2) Inflation film containing 10% by mass of cyclic olefin-based resin and 90% by mass of LLDPE1 (Evaluation 1-3) Inflation film containing 30% by mass of cyclic olefin-based resin and 70% by mass of LLDPE1 (Evaluation 1- 4) Inflation film containing 70% by mass of cyclic olefin-based resin and 30% by mass of LLDPE1 (Evaluation 1-5) Inflation film consisting only of cyclic olefin-based resin

  As is clear from the result of FIG. 2A, the water vapor barrier property of the inflation film is improved by including the cyclic olefin-based resin. Therefore, even if the thickness of the sealant layer is made thinner than before, the water vapor barrier property equal to or higher than that of the conventional one can be achieved.

<Evaluation 2>
Inflation films (thickness 50 μm) of the following evaluations 2-1 to 2-4 were prepared, and haze values were measured using a haze guard II (manufactured by Toyo Seiki Seisakusho Co., Ltd.). The measurement results are shown in FIG.
(Evaluation 2-1) Inflation film consisting only of LLDPE1,
(Evaluation 2-2) Inflation film containing 10% by mass of cyclic olefin-based resin and 90% by mass of LLDPE1 (Evaluation 2-3) Inflation film containing 20% by mass of cyclic olefinic resin and 80% by mass of LLDPE1 (Evaluation 2- 4) Inflation film containing 30% by mass of cyclic olefin resin and 70% by mass of LLDPE1

  As is apparent from the result of FIG. 2B, the haze value increases by including the cyclic olefin-based resin. However, according to the present invention, since the thickness of the sealant layer can be reduced, it can be evaluated that the transparency of the self-supporting bag of the present invention is comparable to the conventional one.

<Evaluation 3>
T-die films (thickness 80 μm) of the following evaluations 3-1 to 3-6 were produced by the T-die method, and the same materials were heat-sealed by the method described later, and the heat-seal strength was measured. The measurement results are shown in FIG.
(Evaluation 3-1) T-die film containing 100% by mass of LLDPE2 (Evaluation 3-2) T-die film containing 20% by mass of cyclic olefin-based resin and 80% by mass of LLDPE2 (Evaluation 3-3) 100% by mass of LLDPE3 T die film containing (Evaluation 3-4) 20% by mass of cyclic olefin resin, T die film containing 80% by mass of LLDPE3 (Evaluation 3-5) T die film containing 100% by mass of LDPE (Evaluation 3-6) cyclic T-die film containing 20% by mass of olefin resin and 80% by mass of LDPE

  Using a TP-701 heat seal tester (manufactured by Tester Sangyo Co., Ltd.), a heat seal bar 10 mm wide x 300 m long, the heat seal surfaces of the two T-die films are combined, the seal time is 1 second, and the seal pressure is 0.1 MPa. And sealed at a heat seal temperature of 120 ° C. A sample having a width of 15 mm was cut out from the sealed film, and a 180-degree peel test was performed using Tensilon RTM-100 (Orientec Co., Ltd.) testing machine in which both ends of the sealed film were pulled at 300 mm / min.

  From the results of FIG. 3, it was confirmed that the combination of LLDPE and a cyclic olefin resin shows high heat seal strength, but the combination of LDPE and a cyclic olefin resin shows a significant decrease in heat seal strength. .

<Example 1>
A blown film (thickness 100 μm) containing 10% by mass of a cyclic olefin resin and 90% by mass of LLDPE 1 and a biaxially stretched nylon film were integrated by dry lamination to produce a multilayer film. The multilayer film was heat-sealed and punched to produce a standing pouch having a capacity of 500 ml of Example 1. In addition, it manufactured so that the biaxially stretched nylon film side might become the outer side of a container.

<Example 2>
A standing pouch of Example 2 was produced in the same manner as in Example 1 except that an inflation film containing 15% by mass of a cyclic olefin resin and 85% by mass of LLDPE1 was used.

<Example 3>
A two-layer / three-layer multilayer (thickness: 100 μm) in which a layer made of LLDPE1, a layer made of a mixture of 20% by mass of cyclic olefin resin and 80% by mass of LLDPE1, and a layer made of LLDPE1 are laminated in this order Was produced by coextrusion. The multilayer body and the biaxially stretched nylon film were integrated in the same manner as in Example 1 to produce a multilayer film. Using this multilayer film, a standing pouch was produced in the same manner as in Example 1.

<Example 4>
A standing pouch was produced in the same manner as in Example 3 except that a mixture of 30% by mass of cyclic olefin resin and 70% by mass of LLDPE1 was used when producing the multilayer body.

<Comparative Example 1>
A multi-layer film was manufactured by integrating an inflation film composed of LLDPE1 with a film thickness of 130 μm and a biaxially stretched nylon film in the same manner as in Example 1. Using this multilayer film, a standing pouch was produced in the same manner as in Example 1.

<Evaluation 4>
For each of the multilayer films used in Examples 1 to 4 and Comparative Example 1, the heat seal strength was measured by the same method as in Evaluation 3. The same measurement was performed when the heat seal temperature conditions were 100 ° C, 110 ° C, 120 ° C, and 130 ° C. The measurement results are shown in FIG.

<Evaluation 5>
The standing properties of the standing pouches of Examples 1 to 4 and Comparative Example 1 were visually evaluated in a state where 500 ml of water was filled.

  In both cases, it was confirmed that the shape was stable. Comparative Example 1 is a conventionally known standing pouch. However, according to the present invention, it was confirmed that there is no problem in the stability of the standing pouch even if the thickness of the sealant layer is suppressed.

<Evaluation 6>
For the standing pouches of Examples 1 to 4 and Comparative Example 1, drop tests 1 to 3 were performed.

  Drop test 1 was performed by dropping the standing pouch 2 m in height with the bag bottom facing down. Five of each standing pouch were tested. None of the standing pouches were torn.

  Drop test 2 was performed by dropping the standing pouch 2 m in height with the bag flat portion facing down. Five of each standing pouch were tested. None of the standing pouches were torn.

  Drop test 3 was performed by dropping the standing pouch 2 m in height with the top of the bag facing down. Five of each standing pouch were tested. None of the standing pouches were torn.

  From the results of the above drop test, it was confirmed that the standing pouch of the present invention has a strength equal to or higher than that of the conventional one.

1 Standing Pouch 10 Base Material Layer 11 Sealant Layer

Claims (4)

A base material layer composed of a biaxially stretched nylon film;
And a composed sealant layer of a thermoplastic resin film having a layer containing a cycloolefin resin and linear low density polyethylene,
The thermoplastic resin film is a self-supporting bag containing 10% by mass to 40% by mass of a cyclic olefin resin . The self-supporting bag according to claim 1, wherein the cyclic olefin-based resin is a copolymer of ethylene and norbornene. The self-supporting bag according to claim 2 , wherein the cyclic olefin-based resin has a glass transition point of 60 ° C. or higher and 90 ° C. or lower. A method of reducing the volume of a self-supporting bag comprising a sealant layer comprising linear low density polyethylene,
A method for reducing the volume of a self-supporting bag in which the sealant layer has a layer containing 10% by mass or more and 40% by mass or less of a cyclic olefin resin with respect to the sealant layer .

Images