Patent Application
20240042745
The present disclosure relates to a laminate and a packaging bag.
Various types of packaging materials are used in combination depending on properties of the contents to be packaged, the amount of the contents, post-treatment to protect the contents from deterioration, a method of disposing packaging materials, the form in which packaging materials are transported, a method of opening a package, and the like. The term “package” referred to herein means an article composed of a packaging material and contents accommodated therein.
Examples of packaging bags include standing pouch. Standing pouches can make products stand out on commodity shelves at stores, and the scope of their adoption is expanding. To prevent a standing pouch from bending in the middle and allow the entire surface to be seen, a laminate constituting the pouch is required to have a certain degree of rigidity. In addition, if the content is a liquid, the bag must be strong enough not to break when dropped. To correspond to these functions, laminates in which a polyester film, a nylon film, a polyolefin film, and the like are combined have been used.
However, with the growing awareness of environmental issues in recent years, there has been a growing demand for functions such as resource conservation and reuse of various products, and the same functions are required of laminates used for packaging materials.
One method of reusing a laminate in which various materials are combined is to re-separate each material. However, it is necessary to perform various thermal, chemical, and mechanical actions to separate laminates that have been given a predetermined strength as packaging materials. In addition, to classify the separated materials, it is necessary to use a physical action due to specific gravity or spectroscopic methods that differ depending on materials, which is not efficient.
Examples of other methods include mono-materialization of a packaging material. In other words, this is an effort to configure a laminate from the same type of material and reuse the laminate as an integrated material. Patent Literature 1 discloses a laminate including a uniaxially stretched polyolefin resin film and a polyolefin heat-seal layer. The main object of the present invention is a laminate having easy tearability due to a uniaxially stretched film, but the resulting laminate is made of the same type of resin. However, there are no regulations regarding the strength of a packaging material, and it is possible to laminate films with biaxially stretched nylon, polyester, or the like as necessary, which does not address the issue of achieving mono-materialization.
The present inventors have selected a polyethylene resin as a material for achieving mono-materialization of a packaging material. Under the constraint that various resin materials cannot be used in combination, a laminate including a base material layer and a sealant layer has been produced, and using this laminate, trial production of standing pouches has been repeated. As a result, the present inventors have found a problem that, in the process of producing standing pouches from laminates, the laminates stick to each other, making it difficult to provide the laminates to a bag-making machine. In addition to this, the present inventors have found a problem that, in a process of filling a standing pouch with contents, inner surfaces (sealant layers) of the standing pouch stick to each other, making it difficult to open the pouch.
The present disclosure provides a laminate which is applicable to manufacturing of a packaging bag for which mono-materialization should be achieved, and enables efficient bag making and efficient implementation of a process of filling a packaging bag with contents. In addition, the present disclosure provides a packaging bag containing the above-described laminate.
One aspect of the present disclosure relates to a laminate. This laminate includes, in this order: a base material layer; a first polyethylene resin layer containing a first polyethylene resin and having a melt flow rate of less than 5 g/10 minutes, and a second polyethylene resin layer containing a second polyethylene resin and having a melt flow rate of 5 to 12 g/10 minutes, in which a ratio R2 (Mw/Mn) of a weight-average molecular weight Mw to a number average molecular weight Mn of the second polyethylene resin is 7 or less. The melt flow rate in the present disclosure means a value measured under the conditions of a load of 2.16 kg and a temperature of 190° C. according to the method described in JIS K7210. Mw/Mn of a polyethylene resin can be measured using gel permeation chromatography (GPC).
According to the above-described laminate, the base material layer can constitute the outermost surface, and the second polyethylene resin layer can constitute the innermost surface. The second polyethylene resin layer serves as a sealant layer and plays a role of preventing adhesion. That is, since the molecular weight distribution of the second polyethylene resin constituting the second polyethylene resin layer is relatively sharp, there are few low-molecular-weight components that are likely to express surface adhesiveness. For this reason, even if a certain amount of heat is applied to the second polyethylene resin layer while a base material layer of the other laminate is in contact with the second polyethylene resin layer, the adhesion between the two can be suppressed. In addition, even if a certain amount of heat is applied to second polyethylene resin layers while the second polyethylene resin layers are brought into contact with each other after bag making, the adhesion between the two can be suppressed. The first polyethylene resin layer also serves as a sealant layer. Examples of low-molecular-weight components that can be contained in the second polyethylene resin layer contain a wax-like component having a molecular weight of about several thousands.
Whether the molecular weight distribution of a polyethylene resin is sharp or broad can be evaluated by the ratio (Mw/Mn) of the weight-average molecular weight Mw to the number average molecular weight Mn of the resin. The closer this value is to 1, the sharper the molecular weight distribution, and the larger the value, the broader the molecular weight distribution. If the ratio R2 (Mw/Mn) of the weight-average molecular weight Mw to the number average molecular weight Mn of the second polyethylene resin is 7 or less, the molecular weight distribution of the second polyethylene resin is relatively sharp. By setting the ratio R2 of the second polyethylene resin to this value or less, the second polyethylene resin layer can sufficiently play a role of preventing adhesion.
It is preferable that a thickness Ta of the first polyethylene resin layer and a thickness Tb of the second polyethylene resin layer satisfy conditions below. Since the first polyethylene resin layer is sufficiently thinner than the second polyethylene resin layer, a sealant layer can be efficiently produced through, for example, an inflation method.
2≤Tb/(Ta+Tb)×100≤30
It is preferable that the base material layer contain at least a high-density polyethylene resin layer from the viewpoint of heat resistance of the base material layer. In a case where the polyethylene content in the laminate is 90 mass % or more, it can be said that the laminate is composed of a single material (mono-material). In the present disclosure, a mono-material laminate refers to a laminate in which the mass proportion of a specific material (polyethylene resin) is 90 mass % or higher (preferably 95 mass % or higher). The polyethylene resin content in the laminate can be measured using a Fourier transform infrared spectrophotometer (FT-IR).
One aspect of the present disclosure relates to a packaging bag containing the above-described laminate. This packaging bag can realize a mono-material and enables efficient implementation of a process of filling the packaging bag with contents.
According to the present disclosure, there is provided a laminate which is applicable to manufacturing of a packaging bag for which mono-materialization should be achieved, and enables efficient bag making and efficient implementation of a process of filling a packaging bag with contents. In addition, according to the present disclosure, a packaging bag containing the above-described laminate is provided.
Hereinafter, an embodiment of the present disclosure will be described in detail. Here, a standing pouch will be described as an example of a packaging bag in which mono-materialization is achieved. Standing pouches are used as refill pouches for shampoo, hand soap, detergent, and the like, and pouches for soup, seasonings, and the like. The present disclosure is not limited to the following embodiment.
<Standing Pouch>
The bottom tape 3 has one mountain fold part 3a. That is, when the standing pouch 10 stands on its own, the bottom tape 3 is placed in an inverted V-shape (refer to
A side portion of the standing pouch 10 is composed of a heat-sealed portion 7. The width of the heat-sealed portion 7 is, for example, 5 to 18 mm, and may be 7 to 15 mm. When the width of the heat-sealed portion 7 is 5 mm or more, sufficient sealing strength is likely to be achieved. On the other hand, when the width thereof is 18 mm or less, a sufficient amount of contents of the standing pouch 10 is likely to be ensured.
As shown in
From the viewpoint of recyclability, the polyethylene resin content in the standing pouch 10 is preferably 90 mass % or more. From the viewpoint of achieving a higher degree of mono-materialization, the polyethylene resin content in the standing pouch 10 is more preferably 92 mass % or more and still more preferably 95 mass % or more.
<Laminate>
Both the pair of side body portions 1 and 2 and the bottom tape 3 of the standing pouch 10 are substantially made of a polyethylene resin.
The polyethylene resin content in the laminate 20 is preferably 90 mass % or more. If the polyethylene resin content in the laminate 20 is 90 mass % or more, mono-materialization is likely to be achieved, which is preferable. From such a viewpoint, the polyethylene resin content in the laminate 20 is more preferably 92 to 100 mass % and still more preferably 95 to 100 mass %. If mono-materialization can be achieved, resins are likely to be regenerated, which is preferable. The laminate 20 has an excellent impact resistance due to its soft and stretchable firmness.
[Base Material Layer]
The base material layer L1 is preferably made of an unstretched polyethylene resin film. Since the base material layer L1 is unstretched, the resin has almost no orientation, and is easily stretched against external stresses such as pulling or shearing and difficult to break. The thickness of the base material layer L1 is, for example, 5 to 800 μm, and may be 5 to 500 μm or 10 to 50 μm. The base material layer L1 has a melting point at least 20° C. higher than the second polyethylene resin layer L2b and preferably has a melting point at least 25° C. higher than that. The difference in melting points between the two can suppress melting of the base material layer L1 during the heat-sealing process. The difference in seal rising temperature between the base material layer L1 and the sealant layer L2 is preferably 25° C. or more and more preferably 30° C. or more. The seal rising temperature means the temperature at which sealing strength develops, as shown in
The melting point of the base material layer L1 is preferably 120° C. or higher and more preferably 125° C. or higher. Examples of polyethylene resins constituting the base material layer L1 include a high-density polyethylene resin (HDPE) and a medium-density polyethylene resin (MDPE). Among these, HDPE and MDPE having a density of 0.925 g/cm3 or higher are preferably used from the viewpoint of heat resistance. In particular, a high-density polyethylene resin having a density in a range of 0.93 to 0.98 g/cm3 is preferably used.
The polyethylene resin constituting the base material layer L1 is not limited to those derived from petroleum, but may be partly or wholly a resin material of biological origin (for example, biomass polyethylene in which ethylene of biomass origin is used as a raw material). A method for producing a polyethylene resin of biomass origin is disclosed in, for example, Japanese Unexamined Patent Publication No. 2010-511634. The base material layer L1 may contain commercially available biomass polyethylene (such as Green PE manufactured by Braskem S. A.), or may contain mechanically recycled polyethylene made from used polyethylene products or resins (so-called burrs) produced in the manufacturing process of polyethylene products.
The base material layer L1 may contain components other than the polyethylene resin. Examples thereof include polyamide, polyethylene terephthalate, polypropylene, polyvinyl alcohols, and biodegradable resin materials (for example, polylactic acid, polycaprolactone, polyhydroxyalkanoate, polyglycolic acids, modified polyvinyl alcohols, casein, and modified starch). The base material layer L1 may contain additives such as an antistatic agent, an ultraviolet absorber, a plasticizer, a lubricant, and a colorant. The amount of component other than the polyethylene resin in the base material layer L1 is, based on a total amount of the base material layer L1, preferably 0 to 15 mass % and more preferably 0 to 10 mass %.
The base material layer L1 may be a single layer, or may be formed of a plurality of layers. From the viewpoint of heat resistance, the base material layer L1 preferably contains at least a high-density polyethylene resin layer (a layer containing a high-density polyethylene resin).
[Sealant Layer]
As described above, the sealant layer L2 is constituted by a first polyethylene resin layer L2a and a second polyethylene resin layer L2b. The thickness of the sealant layer L2 is, for example, 40 to 150 μm, and may be 20 to 250 μm.
(First Polyethylene Resin Layer) The first polyethylene resin layer L2a contains a first polyethylene resin and has a melt flow rate of less than 5 g/10 minutes. The melt flow rate of the first polyethylene resin layer L2a is preferably 0.5 g/10 minutes or more and less than 5 g/10 minutes, and more preferably 2 g/10 minutes or more and less than 5 g/10 minutes. A melt flow rate of less than 5 g/10 minutes results in higher melt tension, which facilitates suppressing of wrinkles during processing through an inflation method or the like. That is, it is inferred that, when the sealant layer L2 is heated to melt, the first polyethylene resin layer L2a is less likely to flow than the second polyethylene resin layer L2b, and the first polyethylene resin layer L2a serves as a support base material to maintain high film formation accuracy, resulting in a smooth and highly transparent film.
The ratio R1 (Mw/Mn) of the weight-average molecular weight Mw to the number average molecular weight Mn of the polyethylene resin constituting the first polyethylene resin layer L2a may be, for example, 1 to 12, 1 to 8, 1 to 6, 1 to 5, 1 to 4.5, or 1 to 4. The molecular weight distribution of the first polyethylene resin may be sharper than the molecular weight distribution of the second polyethylene resin. If the molecular weight distribution of the first polyethylene resin is sharp, there are few low-molecular-weight components and such components can be suppressed from appearing on the surface of the sealant layer L2 via the second polyethylene resin layer L2b. In a case where the first polyethylene resin layer L2a and the second polyethylene resin layer L2b are each composed of a single polyethylene resin, if the ratio R1 of the first polyethylene resin is smaller than the ratio R2 of the second polyethylene resin, it can be determined that the molecular weight distribution of the first polyethylene resin is sharper than that of the second polyethylene resin.
The melting point of the first polyethylene resin layer L2a is preferably 120° C. or lower and more preferably 95° C. to 110° C. That is, the first polyethylene resin layer L2a is preferably composed of a polyethylene resin having a melting point of 120° C. or lower and more preferably composed of a polyethylene resin having a melting point of 95° C. to 110° C. The first polyethylene resin layer L2a is preferably composed of a polyethylene resin having a density of less than 0.925 g/cm3 (more preferably 0.900 to 0.920 g/cm3). Specific examples thereof include a linear low-density polyethylene resin (LLDPE) and a very low-density polyethylene resin (VLDPE). A blend of these polyethylene resins may be used.
The first polyethylene resin layer L2a may contain a plurality of polyethylene resins as first polyethylene resins. In the case where the first polyethylene resin layer L2a contains a plurality of polyethylene resins, the first polyethylene resin layer L2a preferably contains at least a polyethylene resin that satisfies at least one of the ranges of the above-described ratio R1, melting point, and density.
The content of the polyethylene resin that satisfies at least one of the ranges of the above-described ratio R1, melting point, and density may be, based on the total mass of the polyethylene resins constituting the first polyethylene resin layer L2a, 60 to 100 mass %, 80 to 100 mass %, 90 to 100 mass %, or 95 to 100 mass %. The content of the polyethylene resin that satisfies at least one of the ranges of the above-described ratio R1, melting point, and density may be substantially 100 mass % (a mode in which a first polyethylene resin layer L2a is made of a polyethylene resin that satisfies at least one of the ranges of the above-described ratio R1, melting point, and density) based on the total mass of the polyethylene resins constituting the first polyethylene resin layer L2a.
The first polyethylene resin layer L2a may contain additives such as an antioxidant, a slipping agent, a flame retardant, an anti-blocking agent, a light stabilizer, a dehydrating agent, a tackifier, a crystal nucleating agent, and a plasticizer. The amount of component other than the polyethylene resins in the first polyethylene resin layer L2a is, based on the total amount of the first polyethylene resin layer L2a, preferably 0 to 15 mass % and more preferably 0 to 10 mass %.
The first polyethylene resin layer L2a is preferably sufficiently thicker than the second polyethylene resin layer L2b. That is, the proportion of the thickness of the first polyethylene resin layer L2a is preferably 70% to 98% based on the total thickness of the sealant layer L2. When this proportion is 70% or higher, the stability of film formation can increase and a smooth film without wrinkles can be supplied. On the other hand, when this proportion is 98% or lower, the second polyethylene resin layer L2b can sufficiently play a role of preventing adhesion. This proportion is more preferably 75% to 95% and still more preferably 80% to 90%.
(Second Polyethylene Resin Layer)
The second polyethylene resin layer L2b contains a second polyethylene resin and has a melt flow rate of 5 to 12 g/10 minutes. The melt flow rate of the second polyethylene resin layer L2b is preferably 5 to 10 g/10 minutes, and more preferably 6 to 9 g/10 minutes. A melt flow rate of 5 g/10 minutes or more results in a low extrusion load during production, less heat generation inside an extruder, and less resin degradation. That is, it is inferred that, when the sealant layer L2 is heated to melt, the second polyethylene resin layer L2b is more likely to flow than the first polyethylene resin layer L2a, thereby providing low-temperature sealability and reducing low-molecular-weight components formed through resin decomposition due to thermal deterioration.
The ratio R2 (Mw/Mn) of the weight-average molecular weight Mw to the number average molecular weight Mn of the second polyethylene resin constituting the second polyethylene resin layer L2b is, 7 or less, and may be 1.5 to 7, 2 to 6, 3 to 6, 4 to 6, 4.5 to 6, or 5 to 6. By setting the ratio R2 of the second polyethylene resin to 7 or less, the second polyethylene resin layer L2b can sufficiently play a role of preventing adhesion. That is, a sharp molecular weight distribution means a low content of low-molecular-weight components. Few low-molecular-weight components reduce tackiness and the melting point rises steeply, which suppresses sticking even when, for example, a certain amount of heat is applied in a state where seal surfaces are brought into contact with each other. A polyethylene resin having a sharp molecular weight distribution can be obtained through, for example, a gas phase polymerization method in which a metallocene catalyst is used.
The melting point of the second polyethylene resin layer L2b is preferably 120° C. or lower and more preferably 95° C. to 110° C. That is, the second polyethylene resin layer L2b is preferably composed of a polyethylene resin having a melting point of 120° C. or lower and more preferably composed of a polyethylene resin having a melting point of 95° C. to 110° C. The second polyethylene resin layer L2b is preferably composed of a polyethylene resin having a density of less than 0.925 g/cm3 (more preferably 0.900 to 0.920 g/cm3). Specific examples thereof include a linear low-density polyethylene resin (LLDPE) and a very low-density polyethylene resin (VLDPE). A blend of these polyethylene resins may be used.
The second polyethylene resin layer L2b may contain a plurality of polyethylene resins as second polyethylene resins. In the case where the second polyethylene resin layer L2b contains a plurality of polyethylene resins, the second polyethylene resin layer L2b preferably contains at least a polyethylene resin that satisfies at least one of the ranges of the above-described ratio R2, melting point, and density.
The content of the polyethylene resin that satisfies at least one of the ranges of the above-described ratio R2, melting point, and density may be, based on the total mass of the polyethylene resins constituting the second polyethylene resin layer L2b, 60 to 100 mass %, 80 to 100 mass %, 90 to 100 mass %, or 95 to 100 mass %. The content of the polyethylene resin that satisfies at least one of the ranges of the above-described ratio R2, melting point, and density may be substantially 100 mass % (a mode in which a second polyethylene resin layer L2b is made of a polyethylene resin that satisfies at least one of the ranges of the above-described ratio R2, melting point, and density) based on the total mass of the polyethylene resins constituting the second polyethylene resin layer L2b.
In a case where the second polyethylene resin layer L2b contains a plurality of polyethylene resins, the content of a polyethylene resin having a ratio R2 exceeding 6 among the second polyethylene resins constituting the second polyethylene resin layer L2b is, based on the total mass of the polyethylene resins constituting the second polyethylene resin layer L2b, preferably 0 to 5 mass % and more preferably 0 to 1 mass %. The second polyethylene resin layer L2b may not contain a polyethylene resin having a ratio R2 exceeding 6.
In a case where the first polyethylene resin layer L2a and/or the second polyethylene resin layer L2b contain a plurality of polyethylene resins, the sharper molecular weight distribution of the first polyethylene resins than that of the second polyethylene resins can be confirmed by the fact that a weighted average value calculated by taking into account the content of each polyethylene resin to the total amount of the first polyethylene resins from the ratio R1 of each polyethylene resin in the first polyethylene resin layer L2a is smaller than a weighted average value calculated by taking into account the content of each polyethylene resin to the total amount of the second polyethylene resins from the ratio R2 of each polyethylene resin in the second polyethylene resin layer L2b.
The second polyethylene resin layer L2b may contain additives such as an antioxidant, a slipping agent, a flame retardant, an anti-blocking agent, a light stabilizer, a dehydrating agent, a tackifier, a crystal nucleating agent, and a plasticizer. The amount of component other than the polyethylene resins in the second polyethylene resin layer L2b is, based on the total amount of the second polyethylene resin layer L2b, preferably 0 to 15 mass % and more preferably 0 to 10 mass %.
The second polyethylene resin layer L2b is preferably sufficiently thinner than the first polyethylene resin layer L2a. That is, the proportion of the thickness of the second polyethylene resin layer L2b is preferably 2% to 30% based on the total thickness of the sealant layer L2. When this proportion is 2% or higher, the second polyethylene resin layer L2b can sufficiently play a role of preventing adhesion. On the other hand, when this proportion is 30% or lower, the sealant layer L2 is likely to be formed. This proportion is more preferably 5% to 25% and still more preferably 10% to 20%.
As some or all of the polyethylene resins constituting the sealant layer L2, biomass polyethylene using ethylene of biomass origin as a raw material may be used. Such a sealant film is disclosed in, for example, Japanese Unexamined Patent Publication No. 2013-177531. The sealant layer L2 may contain mechanically recycled polyethylene made from used polyethylene products or resins (so-called burrs) produced in the manufacturing process of polyethylene products.
(Other Layers)
A laminate may include an adhesive layer (not shown in the drawing) between a base material layer L1 and a sealant layer L2. An adhesive forming the adhesive layer can be selected according to a bonding method, and a urethane adhesive, a polyester adhesive, and the like can be used. By providing such an adhesive layer, the interlayer adhesion between the base material layer L1 and the sealant layer L2 is increased and delamination is less likely to occur, whereby pressure resistance or impact resistance of a pouch can be maintained.
The adhesive layer preferably does not contain chlorine. Since the adhesive layer does not contain chlorine, it is possible to prevent an adhesive or a regenerated resin after recycling from being colored or smelling bad due to heat treatment. A biomass material is preferably used for the adhesive layer from the viewpoint of environmental consideration. In addition, biomass polyethylene can be used for a polyethylene resin. From the viewpoint of environmental consideration, the adhesive preferably does not contain a solvent.
The laminate may further include, for example, a gas barrier layer from the viewpoint of improving gas barrier properties against water vapor or oxygen. The gas barrier layer may be provided between the base material layer L1 and the sealant layer L2, or may be provided on the surface of the base material layer L1 opposite to the sealant layer L2. The amount of water vapor permeation of the laminate may be, for example, 5 g/m2·day or less, 1 g/m2·day or less, or 0.5 g/m2·day or less. The amount of oxygen permeation of the laminate may be, for example, 1 cc/m2·day·atm or less, 0.5 cc/m2·day·atm or less, or 0.2 cc/m2·day·atm or less. The inclusion of a gas barrier layer in the laminate protects contents from deteriorating due to water vapor or oxygen, and the long-term quality is likely to be maintained.
Examples of gas barrier layers include a vapor deposition layer of an inorganic oxide. By using a vapor deposition layer of an inorganic oxide, it is possible to obtain high barrier properties with a very thin layer that does not affect the recyclability of the laminate. Examples of inorganic oxides include aluminum oxide, silicon oxide, magnesium oxide, and tin oxide. From the viewpoints of transparency and barrier properties, an inorganic oxide may be selected from the group consisting of aluminum oxide, silicon oxide, and magnesium oxide. The thickness of a vapor deposition layer of an inorganic oxide can be set to, for example, 5 nm to 100 nm, and may be 10 nm to 50 nm. When the thickness thereof is 5 nm or thicker, the barrier properties are likely to be exhibited favorably, and when the thickness thereof is 100 nm or thinner, the flexibility of the laminate is easily maintained. A vapor deposition layer can be formed through, for example, a physical vapor phase growth method and a chemical vapor phase growth method.
The laminate may include a metal layer (metal foil) instead of or in addition to the vapor deposition layer of the inorganic oxide. Various metal foils made of aluminum, stainless steel, and the like can be used as metal layers, and among these, aluminum foil is preferable from the viewpoints of moisture-proof properties, workability such as spreadability, costs, and the like. General soft aluminum foil can be used as aluminum foil. Among these, aluminum foil containing iron is preferable from the viewpoints of excellent pinhole resistance and spreadability during molding. In a case where a metal layer is provided, the thickness thereof may be 7 to 50 μm and 9 to 15 μm from the viewpoints of barrier properties, pinhole resistance, and workability.
A laminate may include an anchor coat layer between the base material layer L1 and the sealant layer L2. The anchor coat layer may be a very thin layer that does not affect the recyclability of the laminate, and can be formed using an anchor coat agent. Examples of anchor coat agents include an acrylic resin, an epoxy resin, an acrylic urethane resin, a polyester-polyurethane resin, a polyether-polyurethane resin, and a polyvinyl alcohol resin. As the anchor coat agents, an acrylic urethane resin and a polyester-polyurethane resin are preferable from the viewpoints of heat resistance and interlayer adhesive strength.
The laminate may further include, for example, a printed layer. The printed layer may be provided between the base material layer L1 and the sealant layer L2, or may be provided on the surface of the base material layer L1 opposite to the sealant layer L2. In a case where a printed layer is provided, printing ink that does not contain chlorine is preferably used from the viewpoint of preventing the printed layer from being colored or smelling bad during remelting. In addition, a biomass material is preferably used for a compound contained in a printing ink from the viewpoint of environmental consideration.
The embodiment of the present disclosure has been described above in detail, but the present disclosure is not limited to the above-described embodiment. For example, in the above-described embodiment, a standing pouch has been exemplified as an application target of a laminate, but the laminate according to the embodiment may be applied to manufacture of other packaging bags. For example, one laminate may be folded into two so that sealant layers face each other and then sealed on three sides to form a bag, or two laminates may be stacked so that sealant layers face each other and then heat-sealed on four sides to form a bag. Packaging bags can accommodate contents such as foods and medicaments as contents. Packaging bags can be subjected to heat sterilization treatment such as boiling treatment.
Hereinafter, the present disclosure will be described in more detail with reference to examples. However, the present disclosure is not limited by the following examples.
The following materials were used to produce laminates.
The first seal layer (thickness: 80 μm) was provided on the surface of a support film. A sealant layer having a two-layer structure was obtained by providing the second seal layer (thickness: 20 μm) on the surface of this first seal layer. Each laminate according to Example 1 was obtained by adhering the sealant layer to the base material layer via the adhesive layer (thickness: 1 to 2 μm). After adhering the base material layer to the sealant layer, the above-described support film was peeled off. As a resin constituting the first seal layer, a resin having a sharper molecular weight distribution than that of a resin constituting the second seal layer was used.
Each laminate according to Example 2 was obtained in the same manner as in Example 1 except that the second seal layer was formed using a blend of the following two types of polyethylene resins (density: 0.912 g/cm3, MFR: 5.0 g/10 minutes, melting point: 103° C.).
5 parts by mass of LLDPE and 5 parts by mass of VLDPE were blended. As a resin constituting the first seal layer, a resin having a sharper molecular weight distribution than that of the resins constituting the second seal layer was used.
Each laminate according to Comparative Example 1 was obtained in the same manner as in Example 1 except that a single-layer sealant layer (thickness: 100 μm) was provided using the following polyethylene resin instead of providing the sealant layer having a two-layer structure.
Each laminate according to Comparative Example 2 was obtained in the same manner as in Example 1 except that a single-layer sealant layer (thickness: 100 μm) was provided using the following polyethylene resin instead of providing the sealant layer having a two-layer structure.
<Sealing Strength>
The sealing strengths of the laminates according to the examples and the comparative examples were measured as follows. That is, laminates were overlapped so that the sealant layers faced each other and sealed using a heat sealer having a width of 10 mm. The sealing conditions were pressure: 0.2 MPa and time: 1.0 second. The sealing was performed at a predetermined sealing temperature (from 80° C. to 200° C. at intervals of 10° C.). Each test piece was obtained by cutting the sealed packaging material into a width of 15 mm. A T-peel test was carried out using a tensile tester at a rate of 300 mm/min.
<Manufacture of Standing Pouch>
The laminates according to the examples and the comparative examples were used as main bodies and bottom materials, and standing pouches were manufactured using a bag-making machine manufactured by Totani Corporation. The pouch size was as follows.
In the laminates of Comparative Example 3, the base material layers were thermally fused to a seal bar of the bag-making machine, so it was impossible to make a bag.
(Evaluation of Opening Properties)
The standing pouches according to the examples and the comparative examples were each passed through nip rolls heated to 60° C. under a pressure of 0.5 MPa. Thereafter, a force required to open an opening portion of each standing pouch was measured. The results are shown in Table 2.
(Pressure-Resistance Test)
About 400 mL of normal-temperature water was sealed in each of the standing pouches according to the examples and the comparative examples. Breakage of each bag was confirmed when a static load of 80 kgf was applied to each sealed body for 1 minute. This test was performed 10 times to measure the number of bags broken. The results are shown in Table 2.
(Drop Test)
About 400 mL of normal-temperature water was sealed in each of the standing pouches. Breakage of each bag was confirmed when each sealed body was dropped 10 times from a height of 1 m in an upright position. This test was performed 5 times to measure the number of bags broken. The results are shown in Table 2.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-213965 | Dec 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/047997 | 12/23/2021 | WO |
