Drawn polyethylene film, packaging material, and food package

JP2024051698A5Pending Publication Date: 2025-10-06MITSUI CHEM TOHCELLO INC
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Patent Information

Application Number
JP2022157996
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Filing Date
2022-09-30
Publication Date
2025-10-06

AI Technical Summary

Technical Problem

Existing packaging films face challenges in recycling due to complex multilayer structures, and single-layer polyethylene films lack flexibility, making them difficult to recycle and less environmentally friendly.

Method used

A stretched polyethylene film comprising high-density and medium-density polyethylene layers, optimized through specific thermal processing and layer composition to enhance flexibility, including corona treatment for improved properties.

Benefits of technology

The film achieves improved flexibility, puncture resistance, bending resistance, and tear strength, facilitating easier recycling and environmental sustainability.

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Abstract

To provide a drawn polyethylene film having improved flexibility.SOLUTION: There is provided a drawn polyethylene film comprising a high density polyethylene layer 1 (101), a medium density polyethylene layer (102), and a high density polyethylene layer 2 (103) in this order. When the drawn polyethylene film is continuously subjected to a first differential scanning calorimetry (1stRun), consisting of a temperature increase from -50°C to 200°C at a rate of 10°C / min, an isothermal process at 200°C for 10 minutes, and a temperature decrease from 200°C to -50°C at a rate of 10°C / min, and a second differential scanning calorimetry (2ndRun), consisting of a temperature increase from -50°C to 200°C at a rate of 10°C / min, using a differential scanning calorimeter, an endothermic Peak A is observed in a range of 10°C or more and 160°C or less in a DSC curve 1 obtained by the first differential scanning calorimetry, and the heat of melting (ΔHm) of the endothermic peak A is 110 J / g or more and 162 J / g or less.SELECTED DRAWING: Figure 1
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Description

[Technical field]

[0001] The present invention relates to a stretched polyethylene film, a packaging material, and a food packaging body. Regarding. [Background technology]

[0002] In the field of packaging films, attempts to improve various performances by improving the materials used, layer structures, etc. are known.

[0003] Patent Document 1 discloses a laminated film that includes a base layer and a heat seal layer, has a stiffness of 70 mN or more in the TD direction measured under conditions of a loop length of 50 mm and a push-in length of 10 mm, and has a polyethylene content of 90 mass% or more, and describes that this laminated film can be recycled and can fully ensure the self-supporting properties of a standing pouch.

[0004] Patent Document 2 discloses a polyethylene laminate for use as a packaging material, which comprises at least an oriented polyethylene film, an adhesive layer, and a heat-sealable polyethylene layer, in which the adhesive layer contains a solvent-free adhesive, and the oriented polyethylene film contains at least one of high density polyethylene (HDPE) and medium density polyethylene (MDPE), and describes that this polyethylene laminate for use as a packaging material can significantly reduce the burden on the environment, and has high printability and strength.

[0005] Patent Document 3 discloses a polyethylene co-extruded film comprising a polyethylene film substrate and a polyethylene film layer, the polyethylene film substrate being an electron beam irradiated layer containing polyethylene, a light stabilizer and a crosslinking agent, the polyethylene film layer containing polyethylene, and the surface opposite to the surface on which the polyethylene film substrate is provided having heat sealability, and it is described that this polyethylene co-extruded film can suppress deterioration over time, and further has improved heat resistance and strength.

[0006] Patent Document 4 describes a multilayer film in which a gas barrier layer formed by applying a dispersion liquid containing an inorganic layered compound and a water-soluble polymer onto at least one surface of a base layer made of a thermoplastic resin, an overcoat layer containing a cationic resin and a resin having a hydroxyl group, an adhesive layer, and a sealant layer are laminated in this order, and it is described that this multilayer film has excellent heat sealability and gas barrier properties. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] JP 2022-053864 A [Patent Document 2] Patent Publication No. 2022-079510 [Patent Document 3] JP 2018-008455 A [Patent Document 4] JP 2009-241359 A Summary of the Invention [Problem to be solved by the invention]

[0008] In recent years, with growing environmental awareness, and especially with the focus on the problem of marine plastic pollution, society has been paying closer attention to packaging films. And there is now more demand than ever for the promotion of recycling of packaging films. In other words, there is now a growing demand to design and manufacture packaging films with consideration for "ease of recycling."

[0009] Many of the packaging films to date have achieved the desired effects (strength, gas barrier properties, etc.) by laminating a variety of materials. For example, the multilayer film described in Patent Document 4 has at least four layers: a gas barrier layer, an overcoat layer, an adhesive layer, and a sealant layer. However, laminating a variety of materials makes it difficult to recycle. From the viewpoint of facilitating recycling of packaging films, for example, it is conceivable to make the packaging film have as simple a layer structure as possible.

[0010] In terms of simplifying the layer structure, it is theoretically possible to make the packaging film a "single layer." In addition, there are examples such as Patent Documents 1 to 3 in which, even if it is not a single layer, the packaging film has a multi-layer structure in which a single material is blended at a high content as a whole, taking into consideration ease of recycling. The present inventors conducted a preliminary study on the various properties that may be required for packaging films using polyethylene film, which is a relatively low-cost and versatile packaging material. As a result of the study, it was found that a "single-layer" polyethylene film has poor flexibility.

[0011] The present invention provides an oriented polyethylene film having improved flexibility and a packaging material constructed from such an oriented polyethylene film. [Means for solving the problem]

[0012] [1] A high density polyethylene layer 1; A medium density polyethylene layer; A high density polyethylene layer 2; A stretched polyethylene film comprising, in this order: A first differential scanning calorimeter measurement (1st Run) was performed using a differential scanning calorimeter, which consisted of a process of increasing the temperature from -50°C to 200°C at a rate of 10°C / min, an isothermal process of maintaining the temperature at 200°C for 10 minutes, and a process of decreasing the temperature from 200°C to -50°C at a rate of 10°C / min. A second differential scanning calorimetry run (2nd Run) was performed, which consisted of a heating rate of 10°C / min from -50°C to 200°C. When I continued In the DSC curve 1 obtained by the first differential scanning calorimetry, an endothermic peak A is observed in the range of 10° C. to 160° C., and the heat of fusion of the endothermic peak A (ΔH m ) is 110 J / g or more and 162 J / g or less. [2] The stretched polyethylene film according to [1], wherein a total amount of the high density polyethylene layer 1 and the high density polyethylene layer 2 in the stretched polyethylene film is 25 mass% or more and 85 mass% or less, when the entire stretched polyethylene film is taken as 100 mass%. [3] The density of the high density polyethylene layer 1 and the high density polyethylene layer 2, measured in accordance with JIS K 7112:1999, is 940 kg / m 3 More than 970kg / m 3 The stretched polyethylene film according to [1] or [2], which is as follows: [4] The stretched polyethylene film according to any of [1] to [3], wherein the high-density polyethylene layer 1 and the high-density polyethylene layer 2 each have an MFR of 0.01 g / 10 min or more and 20 g / 10 min or less, as measured in accordance with ASTM D1238 under conditions of 190°C and a load of 2.16 kg. [5] The stretched polyethylene film according to any one of [1] to [4], wherein the medium-density polyethylene layer has an MFR of 0.01 g / 10 min or more and 20 g / 10 min or less, as measured in accordance with ASTM D1238 at 190° C. under a load of 2.16 kg. [6] The stretched polyethylene film according to any one of [1] to [5], wherein the stretched polyethylene film has a full width at half maximum (FWHM) of a peak in the MD direction at a diffraction angle 2θ in the range of 0.2 to 0.4°, as determined by small angle X-ray scattering (SAXS) measurement, of 0.20° or less. [7] The stretched polyethylene film according to any one of [1] to [6], wherein the haze of one sheet of the stretched polyethylene film measured in accordance with JIS K 7136:2000 is 16.0% or less. [8] The stretched polyethylene film according to any one of [1] to [7], wherein the sum of a tensile modulus of elasticity T1 in the MD direction and a tensile modulus of elasticity T2 in the TD direction of the stretched polyethylene film, measured in accordance with JIS K7127:1999 using a tensile tester under conditions of a measurement temperature of 23±2°C, 50±5% RH, and a tensile speed of 5 mm / min, is 1600 MPa or more and 2900 MPa or less. [9] The stretched polyethylene film according to any one of [1] to [8], wherein the stretched polyethylene film has a heat shrinkage rate in the MD direction of 5.5% or less when heated at 100° C. for 15 minutes.

[10] The stretched polyethylene film according to any one of [1] to [9], wherein the stretched polyethylene film has a heat shrinkage rate in the MD direction of 25.0% or less when heated at 120° C. for 15 minutes.

[11] The stretched polyethylene film according to any one of [1] to

[10] , wherein at least one surface of the stretched polyethylene film is a corona-treated surface.

[12] At least one surface of the stretched polyethylene film is a non-corona treated surface, The stretched polyethylene film according to any one of [1] to

[11] , wherein when the corona untreated sides of the stretched polyethylene film are bonded together and heat sealed at 140°C, the heat fusion strength is 4.0 N / 15 mm or less.

[13] The stretched polyethylene film according to any one of [1] to

[12] , wherein the stretched polyethylene film has a laminate strength in the MD direction of 0.7 N / 15 mm or more and 10.0 N / 15 mm or less, as measured in accordance with JIS Z 0238:1998 using a tensile tester under conditions of T-peel and a crosshead speed of 300 mm / min.

[14] The stretched polyethylene film according to any one of [1] to

[13] , wherein the entire thickness of the stretched polyethylene film is 10 μm or more and 100 μm or less.

[15] The stretched polyethylene film according to any one of [1] to

[14] , which is a food packaging film.

[16] A packaging material using the stretched polyethylene film according to any one of [1] to

[15] .

[17]

[16] A packaging material according to the present invention; and a food product within the packaging material. Effect of the Invention

[0013] According to the present invention, a stretched polyethylene film having improved flexibility can be provided. [Brief description of the drawings]

[0014] [Figure 1] FIG. 1 is a cross-sectional view showing a schematic example of a structure of a stretched polyethylene film according to an embodiment of the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] Hereinafter, embodiments of the present invention will be described with reference to the drawings. In this specification, "A to B" indicating a range of values ​​means A or more and B or less unless otherwise specified.

[0016] <Stretched polyethylene film> The stretched polyethylene film (100) according to this embodiment comprises a high density polyethylene layer 1 (101), a medium density polyethylene layer (102), and a high density polyethylene layer 2 (103) in this order. When a first differential scanning calorimetry (1st Run) consisting of a process of increasing the temperature from -50°C to 200°C at a heating rate of 10°C / min, an isothermal process of maintaining the temperature at 200°C for 10 minutes, and a process of decreasing the temperature from 200°C to -50°C at a heating rate of 10°C / min, and a second differential scanning calorimetry (2nd Run) consisting of a process of increasing the temperature from -50°C to 200°C at a heating rate of 10°C / min, are successively performed using a differential scanning calorimeter, an endothermic peak A is observed in the range of 10°C to 160°C in the DSC curve 1 obtained by the first differential scanning calorimetry, and the heat of fusion of the endothermic peak A (ΔHm ) is greater than or equal to 110 J / g and less than or equal to 162 J / g.

[0017] According to the study by the present inventors, a three-layer structure including a high-density polyethylene layer 1, a medium-density polyethylene layer, and a high-density polyethylene layer 2 in this order is used, and the heat of fusion (ΔH m It was found that flexibility can be improved by setting the above range. In this specification, flexibility is expressed by puncture resistance, bending resistance, and tear strength, and can be evaluated based on the balance of performance among puncture resistance, bending resistance, and tear strength. In addition, in this specification, flexibility means that the film is flexible and yet difficult to break or tear.

[0018] In the stretched polyethylene film of this embodiment, the heat of fusion (ΔH m ) is 110 J / g or more, preferably 120 J / g or more, more preferably 130 J / g or more, even more preferably 140 J / g or more, even more preferably 145 J / g or more, even more preferably 150 J / g or more, and is 162 J / g or less, preferably 160 J / g or less, from the viewpoint of further suppressing thickness unevenness of the stretched polyethylene film. The heat of fusion (ΔH m ) is measured as follows: A test piece of about 5.0 mg is cut out from the stretched polyethylene film. Next, the test piece is subjected to a first differential scanning calorimeter measurement (1st Run) consisting of a process of increasing the temperature from -50°C to 200°C at a rate of 10°C / min, an isothermal process of keeping the temperature at 200°C for 10 minutes, and a process of decreasing the temperature from 200°C to -50°C at a rate of 10°C / min under a nitrogen gas flow, and a second differential scanning calorimeter measurement (2nd Run) consisting of a process of increasing the temperature from -50°C to 200°C at a rate of 10°C / min. In the DSC curve 1 obtained by the first differential scanning calorimetry, the heat of fusion (ΔH m ) (J / g) is calculated. Here, the heat quantity of the endothermic peak A is calculated by determining the area enclosed by the melting endothermic curve including the endothermic peak A and the baseline. The baseline is a line obtained by differentiating the Heat Flow with respect to time before and after the endothermic peak A to display the Deriv. Heat Flow, and connecting the point where the change in the Deriv. Heat Flow begins (i.e., the point where the flat region of the Deriv. Heat Flow ends) and the point where the change in the Deriv. Heat Flow ends (i.e., the point where the Deriv. Heat Flow enters the flat region). When multiple endothermic peaks are observed in the range of 10° C. or higher and 160° C. or lower, the maximum peak is regarded as endothermic peak A.

[0019] The materials constituting the stretched polyethylene film will be described below.

[0020] In the stretched polyethylene film according to the present embodiment, the medium density polyethylene layer has a density measured in accordance with JIS K 7112:1999 of preferably 910 kg / m from the viewpoint of further improving the flexibility of the stretched polyethylene film. 3 More preferably, 915 kg / m 3 Above 935kg / m 3 Less than or equal to 932 kg / m 3 Less than 930 kg / m, more preferably 930 kg / m 3 Less than 928 kg / m, more preferably 928 kg / m 3 In the stretched polyethylene film according to the present embodiment, the medium-density polyethylene layer preferably has a density measured in accordance with JIS K 7112:1999 of 917 kg / m or less from the viewpoint of further improving the balance of the performances of flexibility and thermal dimensional stability. 3 More preferably, 918 kg / m 3 That's all.

[0021] The melt flow rate (MFR) of the medium-density polyethylene layer, measured in accordance with ASTM D1238 under conditions of 190°C and a load of 2.16 kg, is preferably 0.01 g / 10 min or more, more preferably 0.1 g / 10 min or more, even more preferably 0.5 g / 10 min or more, and even more preferably 1.0 g / 10 min or more from the viewpoint of further improving processability, and is preferably 20 g / 10 min or less, more preferably 10 g / 10 min or less, even more preferably 5 g / 10 min or less, and even more preferably 4 g / 10 min or less, from the viewpoint of improving the stiffness of the stretched polyethylene film while maintaining the tearability of the stretched polyethylene film.

[0022] The melting point of the medium-density polyethylene layer, as measured by a differential scanning calorimeter (DSC), is preferably 110°C or higher, and more preferably 115°C or higher, from the viewpoint of improving heat resistance and stiffness while maintaining processability and adhesion, and is preferably 135°C or lower, more preferably 130°C or lower, and even more preferably 128°C or lower, from the viewpoint of improving adhesion while maintaining heat resistance.

[0023] When two or more types of polyethylene are used as the polyethylene constituting the medium-density polyethylene layer, the density, MFR and melting point of the medium-density polyethylene layer can be measured values ​​for a mixture obtained by melt-blending two or more types of polyethylene by a known method. The melting point of the medium-density polyethylene layer can be the peak temperature of the maximum melting peak.

[0024] In the stretched polyethylene film of this embodiment, the total amount of high density polyethylene layer 1 and high density polyethylene layer 2 is, from the viewpoint of further improving the performance balance of transparency, rigidity, heat resistance, slip property, heat fusion strength and flexibility, preferably 25% by mass or more, more preferably 30% by mass or more, even more preferably 35% by mass or more, even more preferably 40% by mass or more, and even more preferably 45% by mass or more, based on the entire stretched polyethylene film; and, from the viewpoint of further improving the flexibility of the stretched polyethylene film, it is preferably 85% by mass or less, more preferably 83% by mass or less, even more preferably 80% by mass or less, even more preferably 70% by mass or less, and even more preferably 65% ​​by mass or less.

[0025] In the stretched polyethylene film of this embodiment, the high-density polyethylene layer 1 and the high-density polyethylene layer 2 may be formed using the same material or different materials. However, if different materials are used, it is preferable that the high-density polyethylene layer 1 and the high-density polyethylene layer 2 satisfy the following configuration.

[0026] From the viewpoint of further improving the balance of performance among transparency, rigidity, heat resistance, slip property and heat fusion strength, the content of high density polyethylene in the high density polyethylene layer 1 and the high density polyethylene layer 2 is preferably 80% by mass or more, more preferably 85% by mass or more, even more preferably 90% by mass or more, even more preferably 95% by mass or more, and even more preferably 98% by mass or more, based on the entire high density polyethylene layer 1 and the high density polyethylene layer 2. There is no upper limit to the content of high density polyethylene in the high density polyethylene layer 1 and the high density polyethylene layer 2, but it is, for example, 100% by mass or less.

[0027] The density of the high density polyethylene layer 1 and the high density polyethylene layer 2, as measured in accordance with JIS K 7112:1999, is preferably 940 kg / m, from the viewpoint of achieving a better balance of various properties such as heat resistance, transparency, mechanical properties, and rigidity. 3 More preferably, 943 kg / m3 More preferably, 945 kg / m 3 From the viewpoint of achieving a better balance between flexibility and rigidity, it is preferably 970 kg / m 3 Less than or equal to 968 kg / m 3 Less than 965 kg / m, more preferably 965 kg / m 3 Less than 960 kg / m, more preferably 960 kg / m 3 Less than 955 kg / m, more preferably 955 kg / m 3 Less than 950 kg / m, more preferably 950 kg / m 3 The following is the result.

[0028] The density of the high density polyethylene constituting the high density polyethylene layer 1 and the high density polyethylene layer 2, as measured in accordance with JIS K 7112:1999, is preferably 940 kg / m, from the viewpoint of achieving a better balance of various properties such as heat resistance, transparency, mechanical properties, and rigidity. 3 More preferably, 943 kg / m 3 More preferably, 945 kg / m 3 From the viewpoint of achieving a better balance between flexibility and rigidity, it is preferably 970 kg / m 3 Less than or equal to 968 kg / m 3 Less than 965 kg / m, more preferably 965 kg / m 3 Less than 960 kg / m, more preferably 960 kg / m 3 Less than 955 kg / m, more preferably 955 kg / m 3 Less than 950 kg / m, more preferably 950 kg / m 3 The following is the result.

[0029] The melt flow rates (MFR) of the high-density polyethylene layer 1 and the high-density polyethylene layer 2, measured in accordance with ASTM D1238 under conditions of 190°C and a load of 2.16 kg, are preferably 0.01 g / 10 min or more, more preferably 0.1 g / 10 min or more, and even more preferably 0.5 g / 10 min or more, from the viewpoint of further improving fluidity and moldability, and are preferably 20 g / 10 min or less, more preferably 10 g / 10 min or less, even more preferably 5 g / 10 min or less, even more preferably 3 g / 10 min or less, and even more preferably 2 g / 10 min or less, from the viewpoint of improving the stiffness of the stretched polyethylene film while maintaining the tearability of the stretched polyethylene film.

[0030] The melt flow rate (MFR) of the high density polyethylene constituting the high density polyethylene layer 1 and the high density polyethylene layer 2, measured in accordance with ASTM D1238 under conditions of 190°C and a load of 2.16 kg, is preferably 0.01 g / 10 min or more, more preferably 0.1 g / 10 min or more, and even more preferably 0.5 g / 10 min or more, from the viewpoint of further improving fluidity and moldability, and is preferably 20 g / 10 min or less, more preferably 10 g / 10 min or less, even more preferably 5 g / 10 min or less, even more preferably 3 g / 10 min or less, and even more preferably 2 g / 10 min or less, from the viewpoint of improving the stiffness of the stretched polyethylene film while maintaining the tearability of the stretched polyethylene film.

[0031] The melting points of the high-density polyethylene layer 1 and the high-density polyethylene layer 2, as measured by a differential scanning calorimeter (DSC), are preferably 120°C or higher, more preferably 125°C or higher, and preferably 135°C or lower, more preferably 133°C or lower, from the viewpoint of further improving the balance of thermal dimensional stability, heat resistance, mechanical properties, rigidity, bag-formability, fluidity, moldability, and the like.

[0032] The melting points of the high-density polyethylene constituting the high-density polyethylene layer 1 and the high-density polyethylene layer 2, as measured by a differential scanning calorimeter (DSC), are preferably 120°C or higher, more preferably 125°C or higher, and preferably 135°C or lower, more preferably 133°C or lower, from the viewpoint of further improving the balance of thermal dimensional stability, heat resistance, mechanical properties, rigidity, bag-formability, fluidity, moldability, and the like.

[0033] When two or more types of polyethylene are used as the polyethylene constituting the high-density polyethylene layer, the density, MFR and melting point of the high-density polyethylene layer can be measured values ​​for a mixture obtained by melt-blending two or more types of polyethylene by a known method. The melting point of the high-density polyethylene layer can be the peak temperature of the maximum melting peak.

[0034] At least one surface of the stretched polyethylene film of this embodiment is preferably a corona-treated surface (a surface modified by corona discharge irradiation). By making at least one surface of the stretched polyethylene film of this embodiment a corona-treated surface, the printing properties, coating properties, lamination properties with other films, etc. of the stretched polyethylene film of this embodiment can be further improved.

[0035] The high density polyethylene layer 1, the high density polyethylene layer 2 and the medium density polyethylene layer may contain various additives within the scope of the present invention, such as heat stabilizers, weather stabilizers, antioxidants, ultraviolet absorbers, lubricants, slip agents, nucleating agents, antiblocking agents, antistatic agents, antifogging agents, pigments, dyes, inorganic or organic fillers, etc.

[0036] From the viewpoint of further improving the balance of transparency, rigidity, heat resistance, slip properties and heat fusion strength, the thickness of the high-density polyethylene layer 1 and the high-density polyethylene layer 2 is preferably 1 μm or more, more preferably 3 μm or more, and preferably 17 μm or less, more preferably 15 μm or less, even more preferably 10 μm or less, and even more preferably 7 μm or less. The thicknesses of high-density polyethylene layer 1 and high-density polyethylene layer 2 may be the same or different, but are preferably the same from the viewpoint of making the mechanical strength of the stretched polyethylene film uniform on the high-density polyethylene layer 1 side and the high-density polyethylene layer 2 side. From the viewpoint of improving the flexibility of the stretched polyethylene film, the thickness of the medium-density polyethylene layer is preferably 2 μm or more, more preferably 3 μm or more, even more preferably 5 μm or more, and even more preferably 8 μm or more, and is preferably 30 μm or less, more preferably 25 μm or less, even more preferably 20 μm or less, even more preferably 15 μm or less, even more preferably 13 μm or less, and even more preferably 11 μm or less. The overall thickness of the stretched polyethylene film is, from the viewpoints of maintaining the tearability and further improving the mechanical strength of the stretched polyethylene film, preferably 10 μm or more, more preferably 13 μm or more, and even more preferably 15 μm or more, and from the viewpoints of further improving the tearability, handleability, formability, bag-making suitability, lightness, etc. of the stretched polyethylene film, it is preferably 100 μm or less, more preferably 70 μm or less, even more preferably 50 μm or less, even more preferably 40 μm or less, even more preferably 30 μm or less, and even more preferably 25 μm or less.

[0037] Next, the physical properties of the stretched polyethylene film will be described.

[0038] In the stretched polyethylene film of the present embodiment, the tensile modulus T1 in the MD direction of the stretched polyethylene film, measured in accordance with JIS K7127:1999 using a tensile tester under conditions of a measurement temperature of 23±2°C, 50±5% RH, and a tensile speed of 5 mm / min, is preferably 800 MPa or more, more preferably 850 MPa or more, even more preferably 900 MPa or more, even more preferably 950 MPa or more, and even more preferably 1000 MPa or more, from the viewpoint of further improving the balance of the thermal dimensional stability, bag formability, handleability, and packaging suitability of the stretched polyethylene film; and from the viewpoint of further improving the balance of the thermal dimensional stability, bag formability, and packaging suitability of the stretched polyethylene film, is preferably 1500 MPa or less, more preferably 1450 MPa or less, even more preferably 1400 MPa or less, and even more preferably 1350 MPa or less. The tensile modulus T2 in the TD direction of the stretched polyethylene film is, from the viewpoint of further improving the balance of the formability, mechanical properties, transparency, bag-formability, handleability and packaging suitability of the stretched polyethylene film, preferably 700 MPa or more, more preferably 750 MPa or more, even more preferably 800 MPa or more, even more preferably 850 MPa or more, and even more preferably 900 MPa or more, and from the viewpoint of further improving the balance of the bag-formability and packaging suitability of the stretched polyethylene film, preferably 1400 MPa or less, more preferably 1300 MPa or less, even more preferably 1200 MPa or less, and even more preferably 1150 MPa or less.

[0039] In the stretched polyethylene film of the present embodiment, the total value of the tensile modulus of elasticity T1 in the MD direction and the tensile modulus of elasticity T2 in the TD direction of the stretched polyethylene film, which is measured using a tensile tester in accordance with JIS K7127:1999 under conditions of a measurement temperature of 23±2°C, 50±5% RH, and a tensile speed of 5 mm / min, is preferably 1600 MPa or more, more preferably 1700 MPa or more, even more preferably 1800 MPa or more, from the viewpoint of improving the balance of performance among transparency, rigidity, heat resistance, heat fusion strength, and thermal dimensional stability, and further improving the stiffness of the stretched polyethylene film. It is preferably 1900 MPa or more, more preferably 2000 MPa or more, and even more preferably 2050 MPa or more. From the viewpoint of preventing problems such as breakage during molding of the stretched polyethylene film, facilitating continuous stretch molding of the film, and further improving industrial continuous productivity, it is preferably 2900 MPa or less, more preferably 2800 MPa or less, even more preferably 2700 MPa or less, even more preferably 2600 MPa or less, even more preferably 2500 MPa or less, and even more preferably 2400 MPa or less. Such a tensile modulus is a substitute value for quantitatively measuring the stiffness of a film, and can be adjusted, for example, by adjusting the types and contents of the high density polyethylene layer 1, high density polyethylene layer 2, and medium density polyethylene layer contained in the stretched polyethylene film, the thickness of the stretched polyethylene film, the stretching ratio, etc.

[0040] In the stretched polyethylene film of this embodiment, the haze per sheet of stretched polyethylene film measured in accordance with JIS K 7136: 2000 is preferably 16.0% or less, more preferably 15.8% or less, even more preferably 15.5% or less, even more preferably 15.3% or less, and even more preferably 15.0% or less, from the viewpoint of further improving the transparency of the stretched polyethylene film. There is no lower limit for the haze per sheet of stretched polyethylene film, but it is, for example, 0.1% or more, may be 1.0% or more, 3.0% or more, or may be 5.0% or more.

[0041] In the stretched polyethylene film of this embodiment, the full width at half maximum (FWHM) of the peak in the MD direction diffraction angle 2θ range of 0.2 to 0.4°, as determined by small angle X-ray scattering (SAXS) measurement, is preferably 0.20° or less from the viewpoint of increasing the crystallinity of the surface layer of the stretched polyethylene film to suppress the formation of a brittle layer and improving slip properties. The full width at half maximum (FWHM) of the peak in the MD direction diffraction angle 2θ range of 0.2 to 0.4° of the stretched polyethylene film is preferably 0.05° or more, more preferably 0.10° or more, even more preferably 0.13° or more, and even more preferably 0.15° or more, from the viewpoint of further improving film formability, bag formability, laminate strength, and thermal dimensional stability. The full width at half maximum (FWHM) of the peak in the MD direction diffraction angle 2θ range of 0.2 to 0.4° obtained from such small angle X-ray scattering (SAXS) measurement can be adjusted, for example, by adjusting the types and contents of the high density polyethylene layer 1, high density polyethylene layer 2 and medium density polyethylene layer contained in the stretched polyethylene film, the thickness and stretch ratio of the stretched polyethylene film, etc.

[0042] In the stretched polyethylene film of this embodiment, the heat shrinkage rate in the MD direction of the stretched polyethylene film when heated at 100°C for 15 minutes is, from the viewpoint of further improving the thermal dimensional stability and bag-formability, preferably 5.5% or less, more preferably 5.0% or less, even more preferably 4.5% or less, even more preferably 4.3% or less, and even more preferably 4.1% or less, and may be 0.1% or more, 0.5% or more, 1.0% or more, 1.5% or more, or 2.0% or more. In addition, the heat shrinkage rate of the stretched polyethylene film can be measured in accordance with JIS C2151:2019.

[0043] In the stretched polyethylene film of this embodiment, the heat shrinkage rate in the MD direction of the stretched polyethylene film when heated at 120°C for 15 minutes is, from the viewpoint of further improving the thermal dimensional stability and bag-formability, preferably 25.0% or less, more preferably 23.0% or less, and even more preferably 22.0% or less, and may be 1.0% or more, 5.0% or more, 10.0% or more, or 15.0% or more.

[0044] When at least one of the stretched polyethylene films is not corona-treated, the heat fusion strength when the non-corona-treated sides of the stretched polyethylene films are bonded together and heat-sealed at 140° C. is preferably 4.0 N / 15 mm or less, more preferably 3.8 N / 15 mm or less, from the viewpoint of improving heat resistance. There is no lower limit to the heat fusion strength, but it is, for example, 0.1 N / 15 mm or more. The heat fusion strength is measured as follows. The non-corona treated surfaces of two sheets of stretched polyethylene film cut to a width of 15 mm are heat-sealed to each other at 140°C, a pressure of 2.0 kgf, and a sealing time of 1.0 second to obtain a laminated film. Next, the two sheets of stretched polyethylene film are peeled off using the laminated film cut to a width of 15 mm under conditions of 90° peeling, a peeling speed of 300 mm / min, and tension in the MD direction, and the peel strength at this time is taken as the heat fusion strength (N / 15 mm).

[0045] In the stretched polyethylene film of the present embodiment, the lamination strength measured in accordance with JIS Z 0238:1998 is, from the viewpoint of achieving a better balance between adhesiveness and easy-opening property, preferably 0.7 N / 15 mm or more, more preferably 0.8 N / 15 mm or more, and is preferably 10.0 N / 15 mm or less, more preferably 5.0 N / 15 mm or less, even more preferably 3.0 N / 15 mm or less, and even more preferably 2.0 N / 15 mm or less. The laminate strength is measured as follows. A 297 cm x 210 cm test piece is cut out from the stretched polyethylene film, and the corona-treated side of the test piece is bonded to the corona-treated side of a 50 μm-thick cast LLDPE film, one side of which has been corona-treated, with an ester adhesive, and aged for 3 days at 40° C. Next, a 15 mm-wide test piece is cut out, and the peel strength is determined when peeled in the MD direction using a tensile tester in accordance with JIS Z 0238:1998 at a peel angle of 90°, a chuck distance of 100 mm, and a crosshead speed of 300 mm / min, and this is taken as the laminate strength.

[0046] In the stretched polyethylene film of this embodiment, the static friction coefficient (tan θ) of the surface of the stretched polyethylene film, measured by a slip tester, is preferably 0.20 or more, more preferably 0.25 or more, and is preferably 0.65 or less, more preferably 0.60 or less, even more preferably 0.55 or less, and even more preferably 0.50 or less. When either the high density polyethylene layer 1 or the high density polyethylene layer 2 of the stretched polyethylene film has been corona treated, the static friction coefficient (tan θ) of the surfaces of the stretched polyethylene film may be measured between treated surfaces, between untreated surfaces, or between treated and untreated surfaces. In particular, from the viewpoint of further improving the handleability of the stretched polyethylene film, it is preferable that the static friction coefficient (tan θ) of the surface on the non-corona treated side of the stretched polyethylene film is within the above range. The static friction coefficient (tan θ) of the surface on the non-corona treated side of the stretched polyethylene film is preferably 0.20 or more, more preferably 0.25 or more, and is preferably 0.65 or less, more preferably 0.60 or less, even more preferably 0.55 or less, and even more preferably 0.50 or less.

[0047] The static friction coefficient (tan θ) of the surface of the stretched polyethylene film that has not been subjected to the corona treatment is measured by the following method. Two sheets of stretched polyethylene film cut to a size of 50 mm x 75 mm (hereinafter referred to as stretched polyethylene films 1 and 2) are prepared, and one of them, stretched polyethylene film 1, is fixed to an inclined plate so that the corona-untreated side is facing up. Next, a friction body with a bottom surface (41 mm x 26 mm in size) made of brass is fixed to the center of the surface opposite the corona-untreated side of the other stretched polyethylene film 2, and a weight is attached on top of the friction body so that the mass applied from the friction body to the stretched polyethylene film 2 is 150 g. Next, the corona-untreated sides of the two stretched polyethylene films 1 and 2 are overlapped. Next, the inclined plate is tilted at a speed of 1° / sec, and the value of tan θ is calculated from the angle θ when the upper stretched polyethylene film 2 starts to slide. When measuring the static friction coefficient (tan θ) of the corona-treated surface, the static friction coefficient (tan θ) of the corona-untreated surface is measured in the above-mentioned method for measuring the static friction coefficient (tan θ) of the corona-untreated surface, except that the corona-untreated surface is replaced with the corona-treated surface.

[0048] In the stretched polyethylene film of this embodiment, the puncture strength from the corona-treated surface to the non-corona-treated surface, measured in accordance with JIS Z1707:1997 under conditions of 23±2°C and 50±5% RH, is, from the viewpoint of further suppressing tearing of the package, preferably 2.5 N or more, more preferably 3.0 N or more, even more preferably 4.0 N or more, and is also preferably 8.0 N or less, more preferably 7.8 N or less, even more preferably 7.5 N or less, even more preferably 7.3 N or less, and even more preferably 7.0 N or less.

[0049] The tear strength in the MD direction of the stretched polyethylene film, measured using a light-load tear tester with a test weight of 96.09 g, is preferably 100 mN or more, more preferably 150 mN or more, even more preferably 200 mN or more, even more preferably 230 mN or more, and even more preferably 250 mN or more, from the viewpoint of improving film-forming properties and bag-making processability, and is preferably 500 mN or less, more preferably 490 mN or less, and even more preferably 450 mN or less, from the viewpoint of improving the tearability while maintaining the heat sealability and stiffness of the stretched polyethylene film. In order to achieve such a tear strength, the density, thickness, etc. of each of the high density polyethylene layer 1, the high density polyethylene layer 2 and the medium density polyethylene layer contained in the stretched polyethylene film may be appropriately adjusted. The tear strength in the MD direction is measured as follows. A test piece measuring 63.5 mm in the MD direction and 50 mm in the TD direction is cut out from the stretched polyethylene film. For each test piece, the tear strength in the MD direction (mN) is measured using a light-load tear tester under the following conditions: pendulum weight: 96.09 g, tear length: 12.7 mm, pendulum lift angle: 90°. The light load tear tester may be, for example, Model-D manufactured by Toyo Seiki Seisakusho Co., Ltd.

[0050] In the stretched polyethylene film of the present embodiment, the number of pinholes generated in the stretched polyethylene film is preferably 2500 pieces / m when measured in a bending test of 3000 times using a Gelbo flex tester at a bending angle of 440 degrees, a bending speed of 40 times / min, and an atmosphere of -30°C. 2 Less than or equal to 2300 pieces / m 2 Less than 2200 / m, more preferably 2 Less than 2100 pieces / m, more preferably 2 Less than 2000 / m, more preferably 2 The following is the result. There is no lower limit for the number of pinholes in a stretched polyethylene film, but for example, 100 pinholes / m 2More than 300 pieces / m 2 More than 500 pieces / m 2 More than 800 pieces / m 2 It may be more than that. The number of pinholes generated represents an index of the flex resistance of the stretched polyethylene film of this embodiment, and the fewer the number of pinholes generated, the better the flex resistance. By ensuring that the number of pinholes generated in the stretched polyethylene film is within the above range, the generation of pinholes due to bending during filling at low temperature or transportation at low temperature can be further suppressed. The Gelbo flex tester may be, for example, a product manufactured by Tester Sangyo Co., Ltd.

[0051] <Identification of high density polyethylene layer and medium density polyethylene layer> The fact that the stretched polyethylene film of this embodiment is composed of a high-density polyethylene layer 1, a medium-density polyethylene layer, and a high-density polyethylene layer 2 can be determined, for example, by cutting a cross-section of the stretched polyethylene film and measuring the melting point of each layer. The melting points of the high density polyethylene layer 1 and the high density polyethylene layer 2 are, for example, in the range of 130°C or higher and 140°C or lower, and the melting point of the medium density polyethylene layer is, for example, in the range of 110°C or higher and 129°C or lower.

[0052] <Method of manufacturing stretched polyethylene film> The stretched polyethylene film of the present embodiment is stretched uniaxially or biaxially from the viewpoint of improving the orientation crystallinity and increasing the mechanical strength, and is preferably stretched uniaxially from the viewpoint of improving the productivity. Moreover, by stretching uniaxially in the MD direction, the tensile modulus T1 in the MD direction can be further improved. The stretched polyethylene film can be obtained, for example, by co-extrusion molding a high-density polyethylene resin for forming the high-density polyethylene layer 1, a medium-density polyethylene resin for forming the medium-density polyethylene layer, and a high-density polyethylene resin for forming the high-density polyethylene layer 2, in that order, into a film, and stretching the film obtained by this co-extrusion molding using a known stretched film production method such as a uniaxial stretching method, simultaneous biaxial stretching method, or sequential biaxial stretching method. The molding device and molding conditions are not particularly limited, and conventionally known molding devices and molding conditions can be used. As the molding device, a T-die extruder, a multi-layer T-die extruder, an inflation molding machine, a multi-layer inflation molding machine, etc. can be used. The conditions for the uniaxial stretching method and the biaxial stretching method may be, for example, the manufacturing conditions for known stretched polyethylene films. More specifically, in the case of the uniaxial stretching method, for example, the longitudinal stretching temperature may be set to 100°C to 145°C, and the longitudinal stretching ratio may be set to a range of 4.5 to 6 times. In the case of the sequential biaxial stretching method, for example, the longitudinal stretching temperature may be set to 100°C to 145°C, the longitudinal stretching ratio may be set to a range of 4.5 to 6 times, the transverse stretching temperature may be set to 110°C to 160°C, and the transverse stretching ratio may be set to a range of 9 to 11 times.

[0053] <Applications of oriented polyethylene film / packaging materials / food packaging> Specifically, the stretched polyethylene film of the present embodiment can be suitably used as a food packaging film. The stretched polyethylene film of the present embodiment can also be suitably used as a packaging material. When used as a packaging material, the stretched polyethylene film of the present embodiment may be used alone, or other layers may be laminated to form the packaging material. Examples of other layers include a base layer, a coating layer, an adhesive layer, a heat seal layer, etc. From the viewpoint of ease of recycling, when these layers are laminated, they are preferably formed of a polyethylene-based resin. The packaging material of the present embodiment can also be suitably used for food packaging. The food packaging is used for the purpose of packaging food, for example, and specifically includes the packaging material of the present embodiment and the food inside the packaging material. Depending on the application, only a portion of the food package may be made of the packaging material of this embodiment, or substantially the entire food package may be made of the packaging material of this embodiment.

[0054] There is no particular limitation on the method for producing a food package from the stretched polyethylene film or packaging material, and any method known in the field of packaging materials / packages, such as heat sealing or melt cutting, can be used as appropriate.

[0055] The stretched polyethylene film according to the present embodiment is preferably used for food packaging that requires good flexibility. The food packaging may be in the form of, for example, a two-sided bag or a standing pouch (pouch packaging). These forms are preferred in that they can provide good flexibility.

[0056] Furthermore, when a food package (such as a packaging bag) is formed using the stretched polyethylene film or packaging material of this embodiment, it is preferable that the corona-treated surface is the inner surface and the non-corona-treated surface is the outer surface. As described above, when another layer is laminated on the stretched polyethylene film, it is preferable to laminate it on the corona-treated surface side. That is, when a laminate using the stretched polyethylene film of this embodiment is used for a food package (such as a packaging bag), it is preferable that the stretched polyethylene film side of this embodiment is the outermost layer of the food package.

[0057] There is no limitation on the food to be packaged in the food package, but examples include baked goods, rice confectioneries, snacks, sprinkles, grain powders, and the like.

[0058] Although the embodiments of the present invention have been described above, these are merely examples of the present invention, and various configurations other than those described above can be adopted. Furthermore, the present invention is not limited to the above-described embodiments, and modifications and improvements within the scope of the present invention are included in the present invention. EXAMPLES

[0059] <Raw materials> The raw materials used in the examples and comparative examples are shown below. The density was measured in accordance with JIS K 7112:1999. The MFR was measured in accordance with ASTM D1238 under conditions of 190° C. and a load of 2.16 kg. The melting point was measured using a differential scanning calorimeter (DSC).

[0060] (High density polyethylene) High density polyethylene (HDPE1): Density: 949kg / m 3 , MFR: 1.1g / 10min, Melting point: 130℃ (Medium Density Polyethylene) Medium density polyethylene (MDPE1): Density: 916kg / m 3 , MFR: 2.3g / 10min, Melting point: 116℃ Medium density polyethylene (MDPE2): Density: 918kg / m 3 , MFR: 3.8g / 10min, Melting point: 116℃ Medium density polyethylene (MDPE3): Density: 923kg / m 3 , MFR: 1.5g / 10min, Melting point: 121℃ Medium density polyethylene (MDPE4): Density: 925kg / m 3 , MFR: 1.9g / 10min, Melting point: 122℃ Medium density polyethylene (MDPE5): Density: 937kg / m 3 , MFR: 1.8g / 10min, Melting point: 127℃ Medium density polyethylene (MDPE6): Density: 942kg / m 3 , MFR: 2.9g / 10min, Melting point: 127℃

[0061] <Production of oriented polyethylene film> [Examples 1 to 3 and Comparative Example 1] In the examples and comparative examples, high density polyethylene, medium density polyethylene, and high density polyethylene were extruded in this order into a film shape using the compositions shown in Table 1, and then a cast sheet was obtained by uniaxial stretching. After uniaxial stretching, the high density polyethylene layer 2 side of the cast sheet was subjected to corona treatment to produce a stretched polyethylene film for each example. The extrusion conditions and uniaxial stretching conditions are shown below. Multi-layer extrusion molding machine: 60mmφ multi-layer T-die extrusion molding machine (L / D=27, manufactured by Screw Seiki Co., Ltd.) Extrusion temperature: 230℃, Processing speed: 25m / min Longitudinal stretching temperature: 110~130℃ Longitudinal stretch ratio: 5 times

[0062] The stretched polyethylene films of the respective examples obtained were subjected to the following evaluations, and the results are shown in Table 1.

[0063] <Small angle X-ray scattering (SAXS) measurement of stretched polyethylene film> For the stretched polyethylene film of each example, the MD direction of the film was set to the top and bottom, the TD direction was set to the left and right, and the angle between the X-ray source direction and the film surface was perpendicular. Small angle X-ray scattering (SAXS) measurements were performed with the following equipment and conditions. Equipment: RIGAKU Co., Ltd., Product name: UltimaIV (small angle scattering attachment system) X-ray incidence direction: normal to the film X-ray wavelength: 0.15418nm Optical unit specifications: 1. Optical system selection slit; for small angle scattering 0.03mm (=1 st .slit) 2.DS; Anti-scattering slit 1.00mm (=2 nd .slit) 3. Soller slit on the entrance side; 5° with flexible optical system 4.1 st .~2 ndDistance between slits: 70mm 5.2 nd .~Sample distance: 98mm 6. Vacuum path length: 100 mm (installed on the front of the receiving slit box, on a dedicated stand) 7.RS, SS; scattering slit 0.20mm, receiving slit 0.10mm 8. Camera length: 285mm 9. Soller slit on the light receiving side; 5° flexible optical system used 10. Monochromatization: None (monochromatization at the entrance side by multilayer mirror) 11. Detector: RIGAKU scintillation detector (HV: 762 V) (one-dimensional) X-ray irradiation conditions: A. Scan axis: 2theta B. Measurement method: Continuous C. Scan start angle: 0.1° D. Scan end angle: 1.0° E. Sampling width: 0.02° F. Scan speed: 0.5° / min G. Voltage and current: 40kV-40mA H. Number of sample stacks: In order to obtain sufficient scattering intensity, the samples were stacked to a distance of approximately 0.5 mm with the sample orientation aligned. The X-ray scattering pattern obtained under the above measurement conditions was corrected for air scattering by the detector to obtain the SAXS profile I(q). The diffraction angle θ was calculated from the magnitude of the scattering vector of the peak derived from the crystal long period of the SAXS profile I(q) using equation (1), and this was substituted into Bragg's equation (2) to calculate the crystal long period (d). q = 4π sinθ / λ (1) θ: Diffraction angle q: magnitude of scattering vector λ: X-ray wavelength 2dsinθ=λ (2) d: Crystal long period θ: Diffraction angle λ: X-ray wavelength In addition, referring to the structural analysis of crystalline polymer materials by scattering method in Nichias Technical Review (2014) Vol. 2 No. 365, the electron density correlation function γ(r) was calculated by Fourier transforming the SAXS profile I(q) using the following (3). γ(r) has a special property that can be directly used for structural characterization, and the amorphous thickness (da) of each example of the stretched polyethylene film obtained as structural information was calculated. Also, r indicates distance (nm).

[0064]

number

[0065] The difference value of the amorphous thickness from the crystal long period (d) was calculated as the crystal thickness (dc). The full width at half maximum (FWHM) of the peak in the range of 0.2 to 0.4° diffraction angle 2θ in the MD direction was calculated using X-ray analysis software PDXL-2 (RIGAKU). Specifically, air scattering was removed from the SAXS profile I(q) obtained above. The obtained values ​​were separated into crystalline scattering and amorphous scattering using the above software, and the full width at half maximum (FWHM) of the peak in the range of 0.2 to 0.4° diffraction angle 2θ in the MD direction was calculated from the peak fitting results of crystalline scattering according to the following (analysis conditions). (Analysis conditions) Fitting peak shapes: Split pseudo-Voigt function Crystallite size distribution type: Lorentz model

[0066] <Differential scanning calorimetry> A test piece of about 5.0 mg was cut out from each stretched polyethylene film. Next, a differential scanning calorimeter (product name: Q200DSC, manufactured by TA Instruments) was used to perform a first differential scanning calorimeter measurement (1st Run) consisting of a process of increasing the temperature from -50°C to 200°C at a temperature increase rate of 10°C / min, an isothermal process of maintaining the temperature at 200°C for 10 minutes, and a process of decreasing the temperature from 200°C to -50°C at a temperature decrease rate of 10°C / min, and a second differential scanning calorimeter measurement (2nd Run) consisting of a process of increasing the temperature from -50°C to 200°C at a temperature increase rate of 10°C / min, under a nitrogen gas flow. In the DSC curve 1 obtained by the first differential scanning calorimetry, the heat of fusion (ΔH m ) (J / g) was calculated.

[0067] <Haze> The haze per sheet of the stretched polyethylene film in each example was measured using a haze meter (NDH5000, manufactured by Nippon Denshoku Industries Co., Ltd.) in accordance with JIS K7136:2000.

[0068] <Tensile modulus> A test piece measuring 15 mm x 15 cm was cut out from each stretched polyethylene film. The tensile modulus of elasticity in the MD direction T1 and the tensile modulus of elasticity in the TD direction T2 of the test piece were measured in accordance with JIS K7127:1999 at a measurement temperature of 23±2°C, 50±5% RH, and a tensile speed of 5 mm / min, using a tensile tester manufactured by Orientec Co., Ltd. The total value of T1 and T2 was calculated from the obtained values.

[0069] <Heat shrinkage in the MD direction of stretched polyethylene film at 100℃> The heat shrinkage rate in the MD direction of the stretched polyethylene film at 100°C was measured in accordance with JIS C2151:2019. A test piece measuring 10 cm x 10 cm was cut out from the stretched polyethylene film of each example. The test piece was heated in a constant temperature bath with hot air circulation (manufactured by ADVANTEC, product name: DRM620DE) while hanging without applying any force. The test piece was then heat-treated at 100°C for 15 minutes. The length of the test piece in the MD direction after the heat treatment was measured. 100 [cm], and the thermal shrinkage rate in the MD direction [%] is 100 × (10-MD 100 The above measurement was carried out three times, and the average value of the obtained measurements was used as the heat shrinkage rate of the stretched polyethylene film at 100°C.

[0070] <Heat shrinkage in the MD direction of stretched polyethylene film at 120℃> The heat shrinkage rate in the MD direction of the stretched polyethylene film at 120°C was measured in accordance with JIS C2151:2019. A test piece measuring 10 cm x 10 cm was cut out from the stretched polyethylene film of each example. The test piece was heated in a hot air circulation thermostatic chamber (manufactured by ADVANTEC, product name: DRM620DE) while hanging without applying force. The test piece was then heat-treated at 120°C for 15 minutes. The length of the test piece in the MD direction after the heat treatment was measured. 120 [cm], and the thermal shrinkage rate in the MD direction [%] is 100 × (10-MD 120 The above measurement was carried out three times, and the average value of the obtained measurements was used as the heat shrinkage rate of the stretched polyethylene film at 120°C.

[0071] <Static friction coefficient> Two pieces of stretched polyethylene film of each example cut to a size of 50 mm x 75 mm (hereinafter referred to as stretched polyethylene film 1 and 2) were prepared, and one of them, stretched polyethylene film 1, was fixed to an inclined plate so that the corona untreated side was on top. Next, a friction body with a bottom surface (size 41 mm x 26 mm) made of brass was fixed to the center of the surface opposite to the corona untreated side of the other stretched polyethylene film 2, and a weight was attached on top of the friction body so that the mass applied from the friction body to the stretched polyethylene film 2 was 150 g. Next, the corona untreated sides of the two stretched polyethylene films 1 and 2 were overlapped. Next, the inclined plate was inclined at a speed of 1° / sec, and the value of tan θ was calculated from the angle θ when the upper stretched polyethylene film 2 started to slide, and this was used as the static friction coefficient of the corona untreated surface.

[0072] <Heat fusion strength> Two sheets of stretched polyethylene film of each example cut to a width of 15 mm were heat-sealed together with their corona-untreated surfaces at 140°C, a pressure of 2.0 kgf, and a sealing time of 1.0 second to obtain a laminated film. The obtained laminated film was then cut to a width of 15 mm, and the two sheets of stretched polyethylene film were peeled off under the conditions of 90° peeling, a peeling speed of 300 mm / min, and tension in the MD direction, and the peel strength at this time was recorded as the heat-sealing strength (N / 15 mm).

[0073] <Lamination strength> A test piece of 297 cm x 210 cm was cut out from the stretched polyethylene film of each example, and the corona-treated side of the test piece was bonded to the corona-treated side of a 50 μm-thick cast LLDPE film (manufactured by Mitsui Chemicals Tohcello, TUX FCS #50) with one side corona-treated with an ester-based adhesive (Mitsui Chemicals Takelac A310 / Takenate A3 / ethyl acetate) = 12 / 1 / 7), and aged at 40 ° C for 3 days. Next, a test piece was cut out to a width of 15 mm, and the peel strength was measured using a tensile tester (Orientec Co., Ltd. Tensilon universal tester RTC-1225) in accordance with JIS Z 0238: 1998 at a peel angle of 90 °, a chuck distance of 100 mm, and a crosshead speed of 300 mm / min in the MD direction, and this was taken as the laminate strength.

[0074] <Puncture strength> As an index of flexibility, the puncture strength was measured as follows. Test pieces measuring 60 mm in width and 200 to 300 mm in length were cut out from each stretched polyethylene film. Then, the puncture strength (N) from the corona-treated surface to the corona-untreated surface was measured under conditions of 23±2°C and 50±5% RH in accordance with JIS Z1707:1997 using a Tensilon RTC-1225 manufactured by Orientec Co., Ltd.

[0075] <Bending performance> As an index of flexibility, bending resistance was evaluated as follows. A test piece measuring 297 cm x 210 cm was cut out from the stretched polyethylene film of each example, and a bending test was performed 3,000 times using a Gelbo Flex Tester (manufactured by Tester Sangyo Co., Ltd.) at a bending angle of 440 degrees and a bending speed of 40 times / minute in an atmosphere of -30°C. After the bending test, bags were made from the test pieces, and the number of pinholes generated was measured using Ageless Seal Check Liquid (manufactured by Mitsubishi Gas Chemical Co., Ltd.).

[0076] <Tear strength> As an index of flexibility, tear strength was measured as follows. A test piece of 63.5 mm in MD and 50 mm in TD was cut out from each stretched polyethylene film. The tear strength (mN) in MD was measured for each test piece using a light-load tear tester (manufactured by Toyo Seiki Seisakusho Co., Ltd., Model-D) under the following conditions: pendulum weight: 96.09 g, tear length: 12.7 mm, pendulum lift angle: 90°.

[0077] The flexibility of the stretched polyethylene films was evaluated according to the following criteria. (standard) A (Good): Meets all of the following (i) to (iii) B (Poor): One or more of the following items (i) to (iii) are not met. (i) The puncture strength is 2.5 N or more. (ii) Bending resistance (number of pinholes) is 2,500 / m 2 The following is the result. (iii) The tear strength in the MD direction is 100 mN or more.

[0078] [Table 1]

[0079] When the stretched polyethylene film of the example was used, a food packaging film with improved flexibility (performance balance of puncture strength, bending resistance and tear strength) could be obtained. [Explanation of symbols]

[0080] 100 Stretched polyethylene film 101 High density polyethylene layer 1 102 Medium density polyethylene layer 103 High density polyethylene layer 2

Claims

1. a high-density polyethylene layer 1; a medium density polyethylene layer; a high-density polyethylene layer 2; A stretched polyethylene film comprising, in this order: A first differential scanning calorimetry (1st Run) was performed using a differential scanning calorimeter, which consisted of a process of increasing the temperature from -50°C to 200°C at a temperature increase rate of 10°C / min, an isothermal process of maintaining the temperature at 200°C for 10 minutes, and a process of decreasing the temperature from 200°C to -50°C at a temperature decrease rate of 10°C / min. A second differential scanning calorimetry (2nd Run) consisting of a temperature increase from -50°C to 200°C at a temperature increase rate of 10°C / min; When I continued In the DSC curve 1 obtained by the first differential scanning calorimetry, an endothermic peak A is observed in the range of 10°C or higher and 160°C or lower, and the heat of fusion of the endothermic peak A (ΔH m ) is 110 J / g or more and 162 J / g or less.

2. 2. The stretched polyethylene film according to claim 1, wherein the total amount of the high-density polyethylene layer 1 and the high-density polyethylene layer 2 in the stretched polyethylene film is 25% by mass or more and 85% by mass or less, when the entire stretched polyethylene film is taken as 100% by mass.

3. The densities of the high-density polyethylene layer 1 and the high-density polyethylene layer 2 measured in accordance with JIS K 7112:1999 are each 940 kg / m 3 More than 970kg / m 3 3. The stretched polyethylene film according to claim 1, wherein:

4. 3. The stretched polyethylene film according to claim 1, wherein the high-density polyethylene layer 1 and the high-density polyethylene layer 2 each have an MFR of 0.01 g / 10 min or more and 20 g / 10 min or less, as measured in accordance with ASTM D1238 at 190°C under a load of 2.16 kg.

5. 3. The stretched polyethylene film according to claim 1, wherein the medium-density polyethylene layer has an MFR of 0.01 g / 10 min or more and 20 g / 10 min or less, as measured in accordance with ASTM D1238 at 190°C under a load of 2.16 kg.

6. 3. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a peak full width at half maximum (FWHM) of 0.20° or less in the MD direction at a diffraction angle 2θ in the range of 0.2 to 0.4°, as determined by small-angle X-ray scattering (SAXS) measurement.

7. 3. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a haze of 16.0% or less per sheet as measured in accordance with JIS K 7136:2000.

8. The tensile modulus T of the stretched polyethylene film in the MD direction is measured using a tensile tester in accordance with JIS K7127:1999 under the conditions of a measurement temperature of 23±2°C, 50±5% RH, and a tension speed of 5 mm / min. 1 and the tensile modulus in the TD direction T 2 The stretched polyethylene film according to claim 1 or 2, wherein the total value of is 1600 MPa or more and 2900 MPa or less.

9. 3. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a heat shrinkage rate in the machine direction of 5.5% or less when heated at 100°C for 15 minutes.

10. 3. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a heat shrinkage rate in the machine direction of 25.0% or less when heat-treated at 120°C for 15 minutes.

11. 3. The stretched polyethylene film according to claim 1, wherein at least one surface of the stretched polyethylene film is a corona-treated surface.

12. At least one surface of the stretched polyethylene film is an uncorona-treated surface, 3. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a heat fusion strength of 4.0 N / 15 mm or less when the non-corona treated surfaces of the stretched polyethylene film are bonded together and heat-sealed at 140°C.

13. 3. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a lamination strength in the machine direction of 0.7 N / 15 mm or more and 10.0 N / 15 mm or less, as measured in accordance with JIS Z 0238:1998 using a tensile tester under conditions of T-peel and a crosshead speed of 300 mm / min.

14. 3. The stretched polyethylene film according to claim 1, wherein the total thickness of the stretched polyethylene film is 10 μm or more and 100 μm or less.

15. 3. The stretched polyethylene film according to claim 1, which is a food packaging film.

16. A packaging material using the stretched polyethylene film according to claim 1 or 2.

17. The packaging material according to claim 16; and a food product within the packaging material.