JP2024051484A - Stretched polyethylene film, packaging material and food packaging body - Google Patents

Abstract

[Problem] To provide a stretched polyethylene film with improved flexibility. [Solution] The stretched polyethylene film includes a high density polyethylene layer 1 (101), a medium density polyethylene layer (102), and a high density polyethylene layer 2 (103) in this order, and has an amorphous thickness of less than 12.5 nm as determined from a peak in the MD direction diffraction angle 2θ range of 0.2 to 0.4° by small angle X-ray scattering (SAXS) measurement. [Selected Figure] Figure 1

Description

The present invention relates to a stretched polyethylene film, a packaging material, and a food package.

In the field of packaging films, attempts to improve various performances by devising materials used and layer structures are known.

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% by mass or more, and describes that this laminated film can be recycled and can fully ensure the self-supporting properties of a standing pouch.

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

Patent Document 3 discloses a polyethylene co-extruded film that includes a polyethylene film substrate and a polyethylene film layer, the polyethylene film substrate being an electron beam irradiated layer that contains 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 has 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.

Patent Document 4 describes a multilayer film in which a gas barrier layer formed by applying a dispersion containing an inorganic layered compound and a water-soluble polymer to 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.

JP 2022-053864 A JP 2022-079510 A JP 2018-008455 A JP 2009-241359 A

In recent years, with growing environmental awareness, and in particular the issue of marine plastic pollution coming into focus, society has been paying closer attention to packaging films. As a result, there is a greater demand than ever before for the promotion of recycling of packaging films. In other words, there is an increasing demand to design and manufacture packaging films with "ease of recycling" in mind.

Many of the conventional packaging films have achieved the desired effects (strength, gas barrier properties, etc.) by laminating various 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 various 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.

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, a multi-layer structure in which a single material is blended at a high content as a whole is used in consideration of 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 is inferior in flexibility.

The present invention provides a stretched polyethylene film with improved flexibility and a packaging material made from such a stretched polyethylene film.

[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 stretched polyethylene film having an amorphous thickness of less than 12.5 nm, as determined from peaks in the MD direction diffraction angle 2θ range of 0.2 to 0.4° by small angle X-ray scattering (SAXS) measurement.
[2]
The stretched polyethylene film according to [1], wherein the stretched polyethylene film has a tensile modulus in a TD direction T2 of 920 MPa or more, as measured using a tensile tester in accordance with JIS K7127:1999 under conditions of a measurement temperature of 23± ₂ °C, a relative humidity of 50±5%, and a tensile speed of 5 mm/min.
[3]
The stretched polyethylene film according to [1] or [2], wherein the medium-density polyethylene layer has a density, as measured in accordance with JIS K 7112:1999, of 910 kg/ ^m3 or more and less than 940 kg/ ^m3 .
[4]
The stretched polyethylene film according to any one of [1] to [3], 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 entirety of the stretched polyethylene film is taken as 100 mass%.
[5]
The stretched polyethylene film according to any one of [1] to [4], wherein the high-density polyethylene layer 1 and the high-density polyethylene layer 2 each have a density, as measured in accordance with JIS K 7112:1999, of 940 kg/ ^m3 or more and 970 kg/ ^m3 or less.
[6]
The stretched polyethylene film according to any one of [1] to [5], wherein the haze per sheet of the stretched polyethylene film measured in accordance with JIS K 7136:2000 is 16.0% or less.
[7]
The stretched polyethylene film according to any one of [1] to [6], wherein the sum of the tensile modulus T1 in the MD direction and the tensile modulus _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 1500 MPa or more and 2900 MPa or less.
[8]
The stretched polyethylene film according to any one of [1] to [7], wherein the stretched polyethylene film has a heat shrinkage rate in the MD direction of 6.0% or less when heat-treated at 100° C. for 15 minutes in accordance with JIS C2151:2019.
[9]
The stretched polyethylene film according to any one of [1] to [8], wherein at least one surface of the stretched polyethylene film is a corona-treated surface.
[10]
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 [9], wherein the heat fusion strength when the non-corona treated surface of the stretched polyethylene film is bonded to the other surface and heat sealed at 140°C is 4.0 N/15 mm or less.
[11]
The stretched polyethylene film according to any one of [1] to [10], wherein the total thickness of the stretched polyethylene film is 10 μm or more and 100 μm or less.
[12]
The stretched polyethylene film according to any one of [1] to [11], which is a film for packaging food.
[13]
A packaging material using the stretched polyethylene film according to any one of [1] to [12].
[14]
[13] The packaging material according to the present invention;
and a food product within the packaging material.

The present invention provides a stretched polyethylene film with improved flexibility.

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.

The following describes an embodiment of the present invention with reference to the drawings. In this specification, unless otherwise specified, "A to B" indicating a numerical range means A or more and B or less.

<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, and has an amorphous thickness of less than 12.5 nm as determined from a peak in a diffraction angle 2θ range of 0.2 to 0.4° in the MD direction by small angle X-ray scattering (SAXS) measurement.

It has been found that the stretched polyethylene film according to this embodiment has a three-layer structure in which the medium-density polyethylene layer is sandwiched between high-density polyethylene layer 1 and high-density polyethylene layer 2, and the amorphous thickness of the stretched polyethylene film is set to the above-mentioned upper limit value or less, thereby making it possible to improve the flexibility of the stretched polyethylene film.
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.

In the stretched polyethylene film according to the present embodiment, the amorphous thickness determined from the peak in the MD direction diffraction angle 2θ range of 0.2 to 0.4° by small angle X-ray scattering (SAXS) measurement is less than 12.5 nm, preferably 12.4 nm or less, more preferably 12.2 nm or less, even more preferably 12.0 nm or less, even more preferably 11.7 nm or less, and even more preferably 11.5 nm or less, from the viewpoint of improving the flexibility of the stretched polyethylene film. There is no lower limit to the amorphous thickness determined from the peak in the MD direction diffraction angle 2θ range of 0.2 to 0.4° by small angle X-ray scattering (SAXS) measurement, but it is, for example, 9.0 nm or more, may be 9.5 nm or more, may be 10.0 nm or more, may be 10.5 nm or more, or may be 11.0 nm or more.
Such amorphous thickness can be adjusted, for example, by adjusting the types and contents 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, the thickness and stretch ratio of the stretched polyethylene film, etc.

The materials that make up the stretched polyethylene film are explained below.

In the stretched polyethylene film according to this embodiment, the total amount of the high-density polyethylene layer 1 and the high-density polyethylene layer 2 is preferably 25% by mass or more, more preferably 30% by mass or more, even more preferably 35% by mass or more, and even more preferably 40% by mass or more, based on the total amount of the stretched polyethylene film, from the viewpoint of further improving the balance between transparency, rigidity, heat resistance, slip properties, and heat fusion strength, and 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 75% by mass or less, even more preferably 65% by mass or less, and even more preferably 60% by mass or less, based on the viewpoint of making the amorphous thickness of the stretched polyethylene film a predetermined value or less and further improving flexibility.

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.

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, respectively, from the viewpoint of further improving the performance balance of transparency, rigidity, heat resistance, slip property, and heat fusion strength. 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, respectively.

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 preferably 940 kg/m or ^more , more preferably 943 kg/m or more, and even more preferably 945 kg/m ^or more, from the viewpoint of achieving a better balance between various performances such as heat resistance, transparency, mechanical properties, and rigidity, and is preferably 970 kg/m ^or less, more preferably 968 kg/m ^or less, even more preferably ⁹⁶⁵ kg/m ^or less, even more preferably 960 kg/m ^or less, even more preferably 955 kg/m or less, and even more preferably 950 kg/m ^{or less} , from the viewpoint of achieving a better balance between flexibility and rigidity.

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 or ^more , more preferably 943 kg/m or more, and even more preferably 945 kg/m ^{or more} , from the viewpoint of achieving a better balance between various performances such as heat resistance, transparency, mechanical properties, and rigidity, and is preferably 970 kg/m or ^less , more preferably 968 kg/m or less, ^even more preferably 965 kg/m ^or less, even more preferably 960 kg/m ^or less, even more preferably 955 kg/m or less, and even more preferably 950 kg/m ^{or less} , from the viewpoint of achieving a better balance between flexibility and rigidity.

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.
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 130° 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.

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.
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 are preferably 135° C. or lower, more preferably 130° 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.

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 using a known method. The melting point of the high-density polyethylene layer can be the peak temperature of the maximum melting peak.

The medium-density polyethylene content in the medium-density polyethylene layer 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 medium-density polyethylene layer, from the viewpoint of keeping the amorphous thickness of the stretched polyethylene film at a predetermined value or less and further improving flexibility. There is no upper limit to the medium-density polyethylene content in the medium-density polyethylene layer, but it is, for example, 100% by mass or less.

The density of the medium-density polyethylene layer, measured in accordance with JIS K 7112:1999, is, from the viewpoint of making the amorphous thickness of the stretched polyethylene film a predetermined value or less and further improving the flexibility, preferably 910 kg/ ^m3 or more, more preferably 913 kg/ ^m3 or more, even more preferably 915 kg/ ^m3 or more, and is preferably less than 940 kg/ ^m3 , more preferably 935 kg/ ^m3 or less, even more preferably 933 kg/ ^m3 or less, and even more preferably 930 kg/ ^m3 or less.

The density of the medium-density polyethylene constituting the medium-density polyethylene layer, measured in accordance with JIS K 7112:1999, is, from the viewpoint of making the amorphous thickness of the stretched polyethylene film a predetermined value or less and further improving the flexibility, preferably 910 kg/ ^m3 or more, more preferably 913 kg/ ^m3 or more, even more preferably 915 kg/ ^m3 or more, and is preferably less than 940 kg/ ^m3 , more preferably 935 kg/ ^m3 or less, even more preferably 933 kg/ ^m3 or less, and even more preferably 930 kg/ ^m3 or less.

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 3 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.
It is.
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 adhesiveness, and is preferably 135° C. or lower, more preferably 130° C. or lower, and even more preferably 125° C. or lower, from the viewpoint of improving adhesiveness while maintaining heat resistance.

The melt flow rate (MFR) of the medium-density polyethylene constituting 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 3 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.
It is.
The melting point of the medium-density polyethylene constituting 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 adhesiveness, and is preferably 135° C. or lower, more preferably 130° C. or lower, and even more preferably 125° C. or lower, from the viewpoint of improving adhesiveness while maintaining heat resistance.

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 using a known method. The melting point of the medium-density polyethylene layer can be the peak temperature of the maximum melting peak.

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

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. Examples of additives include heat stabilizers, weather stabilizers, antioxidants, UV absorbers, lubricants, slip agents, nucleating agents, antiblocking agents, antistatic agents, antifogging agents, pigments, dyes, inorganic or organic fillers, etc.

From the viewpoint of further improving the balance of transparency, rigidity, heat resistance, slip properties and heat fusion strength, the thicknesses of the high-density polyethylene layer 1 and the high-density polyethylene layer 2 are each 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, and 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, and even more preferably 13 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.

Next, we will explain the physical properties of stretched polyethylene film.

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, and packaging suitability of the stretched polyethylene film; and 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, from the viewpoint of further improving the balance of the thermal dimensional stability, bag formability, and packaging suitability of the stretched polyethylene film.
The tensile modulus _T2 in the TD direction of the stretched polyethylene film is preferably 920 MPa or more, more preferably 925 MPa or more, 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, and is preferably 1200 MPa or less, more preferably 1180 MPa or less, even more preferably 1150 MPa or less, and even more preferably 1130 MPa or less, from the viewpoint of further improving the balance of the bag-formability and packaging suitability of the stretched polyethylene film.

In the stretched polyethylene film of this embodiment, the tensile modulus of elasticity in the MD direction T1 and the tensile modulus of elasticity in the TD direction _T2 of the stretched polyethylene film are measured using a tensile tester in accordance with JIS K7127:1999 under conditions of a measurement temperature of 23±2° C., a relative humidity of 50±5%, and a tensile speed of 5 mm/min. From the viewpoints of achieving a better 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, the total value of this is preferably ₁₅₀₀ MPa or more, more preferably 1600 MPa or more, even more preferably 1700 MPa or more, even more preferably 1800 MPa or more, even more preferably 1900 MPa or more, and even more preferably 2000 MPa or more; and from the viewpoints of making troubles such as breakage less likely to occur during molding of the stretched polyethylene film, facilitating continuous stretch molding of the film, and further improving industrial continuous productivity, the total value of this is preferably 2900 MPa or less, more preferably 2700 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.

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 5.0% or more.

In the stretched polyethylene film of this embodiment, the full width at half maximum (FWHM) of the peak in the MD direction at a diffraction angle 2θ of 0.2 to 0.4°, as determined by small angle X-ray scattering (SAXS), is preferably 0.21° or less, more preferably 0.20° or less, even more preferably 0.19° or less, and even more preferably 0.18° 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 the slip properties. The full width at half maximum (FWHM) of the peak in the MD direction at a diffraction angle 2θ 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 the film formability, bag formability, laminate strength, and thermal dimensional stability.
The full width at half maximum (FWHM) of the peak in the MD diffraction angle 2θ range of 0.2 to 0.4°, which is determined 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, the high density polyethylene layer 2, and the medium density polyethylene layer contained in the stretched polyethylene film, the thickness of the stretched polyethylene film, the stretch ratio, etc.

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 6.0% or less, more preferably 5.5% or less, even more preferably 5.0% or less, even more preferably 4.5% or less, even more preferably 4.0% or less, and may be 0.1% or more, 0.5% or more, 1.0% or more, 1.5% or more, 2.0% or more, or 2.5% or more.

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 23.0% or less, more preferably 22.5% or less, and even more preferably 22.0% or less, and may be 1.0% or more, 3.0% or more, 5.0% or more, 10.0% or more, or 15.0% or more.
The heat shrinkage rate of the stretched polyethylene film can be measured in accordance with JIS C2151:2019.

When at least one of the stretched polyethylene films is a non-corona treated surface, the heat fusion strength when the non-corona treated surfaces of the stretched polyethylene films are bonded together and heat fused 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 under conditions of 140°C, pressure of 2.0 kgf, and 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, peeling speed of 300 mm/min, and pulling in the MD direction, and the peel strength at this time is taken as the heat fusion strength (N/15 mm).

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 non-corona treated surface of the stretched polyethylene film is within the above range. The static friction coefficient (tan θ) of the non-corona treated surface 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.

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 pieces of stretched polyethylene film cut to a size of 50 mm x 75 mm (hereinafter referred to as stretched polyethylene film 1 and 2) are prepared, and one of the stretched polyethylene films, the stretched polyethylene film 1, is fixed to an inclined plate so that the corona untreated surface is on top. Next, a friction body with a bottom surface (size 41 mm x 26 mm) made of brass is fixed to the center of the surface opposite to the corona untreated surface 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 surfaces of the two stretched polyethylene films 1 and 2 are overlapped. Next, the inclined plate is inclined 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 the static friction coefficient (tan θ) of the corona-treated surface is measured, 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.

In the stretched polyethylene film of this embodiment, the puncture strength from the corona-treated surface toward the non-corona-treated surface, measured in accordance with JIS Z1707:1997 at 23±2°C and 50±5% RH, is preferably 4.0 N or more, more preferably 4.3 N or more, from the viewpoint of further suppressing tearing of the package, and is preferably 8.0 N or less, more preferably 7.5 N or less, even more preferably 7.0 N or less, even more preferably 6.5 N or less, even more preferably 6.0 N or less, even more preferably 5.5 N or less, even more preferably 5.0 N or less.

The tear strength in the MD direction of the stretched polyethylene film, measured using a light-load tear tester under conditions of test piece size: MD direction: 63.5 mm, TD direction: 50.0 mm, pendulum weight mass: 96.09 g, tear length: 12.7 mm, and pendulum lift angle: 90°, is preferably 100 mN or more, more preferably 150 mN or more, even more preferably 180 mN or more, even more preferably 200 mN or more, and even more preferably 230 mN or more, from the viewpoint of improving film-forming properties and bag-making processability, and is preferably 600 mN or less, more preferably 580 mN or less, even more preferably 550 mN or less, even more preferably 530 mN or less, even more preferably 500 mN or less, even 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 light load tear tester may be, for example, Model D manufactured by Toyo Seiki Seisakusho Co., Ltd.

In the stretched polyethylene film of the present embodiment, the number of pinholes generated in the stretched polyethylene film, as measured using a Gelbo flex tester in a bending test of 3,000 times at a bending angle of 440 degrees and a bending speed of 40 times/min in an atmosphere of -30°C, is preferably 2,700 pcs/m ^or less, more preferably 2,500 pcs/ ^m or less, even more preferably 2,300 pcs/m ^or less, even more preferably 2,100 pcs/m ^or less, and even more preferably 2,000 pcs/m ^or less.
There is no lower limit to the number of pinholes generated in the stretched polyethylene film, but it is, for example, 100 pinholes/ ^m2 or more, or 300 pinholes/ ^m2 or more, or 500 pinholes/ ^m2 or more, or 1000 pinholes/ ^m2 or more.
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.

<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 layers 1 and 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.

<Method of producing 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 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 using a known stretched film production method such as a uniaxial stretching method, simultaneous biaxial stretching method, or sequential biaxial stretching method.
The molding apparatus and molding conditions are not particularly limited, and conventionally known molding apparatus and molding conditions can be used. As the molding apparatus, 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.

<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 the other layers include a base layer, a coating layer, an adhesive layer, and a heat seal layer. 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.

There are no particular limitations on the method for producing food packages from the stretched polyethylene film or packaging material. Methods known in the field of packaging materials/packages, such as heat sealing or melt cutting, can be used as appropriate.

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

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 on the non-corona treated surface side. That is, when a laminate using the stretched polyethylene film of this embodiment is used for a food package (packaging bag, etc.), it is preferable that the stretched polyethylene film side of this embodiment is the outermost layer of the food package.

There is no limit to the foods that can be packaged in the food packaging, but examples include baked goods, rice confectioneries, snacks, sprinkles, grain powders, etc.

The above describes the embodiments of the present invention, but 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.

<Ingredients>
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).

(High density polyethylene)
High density polyethylene (HDPE1): density: 949 kg/m ³ , MFR: 1.1 g/10 min, melting point: 130° C.
(medium density polyethylene)
Medium density polyethylene (MDPE1): density: 916 kg/m ³ , MFR: 2.3 g/10 min, melting point: 116° C.
Medium density polyethylene (MDPE2): density: 918 kg/m ³ , MFR: 3.8 g/10 min, melting point: 116°C
Medium density polyethylene (MDPE3): density: 923 kg/m ³ , MFR: 1.5 g/10 min, melting point: 121° C.
Medium density polyethylene (MDPE4): density: 925 kg/m ³ , MFR: 1.9 g/10 min, melting point: 122°C
Medium density polyethylene (MDPE5): density: 937 kg/m ³ , MFR: 1.8 g/10 min, melting point: 127°C
Medium density polyethylene (MDPE6): density: 942 kg/m ³ , MFR: 2.9 g/10 min, melting point: 127°C

<Production of oriented polyethylene film>
In the examples and comparative examples, high density polyethylene (HDPE1), medium density polyethylene (MDPE1), and high density polyethylene (HDPE1) were extruded in this order into a film shape using the compositions shown in Table 1, and then cast sheets were obtained by uniaxial stretching. The high density polyethylene layer 2 side of the uniaxially stretched cast sheets was then subjected to corona treatment to produce stretched polyethylene films for each example. The extrusion conditions and uniaxial stretching conditions are shown below.
Multi-layer extrusion molding machine: 60 mmφ multi-layer T-die extrusion molding machine (L/D=27, manufactured by Screw Seiki Co., Ltd.)
Extrusion temperature: 230°C, processing speed: 25m/min
Longitudinal stretching temperature: 110 to 130°C
For each of the stretched polyethylene films obtained in the respective examples, the densities of the high density polyethylene layer 1, the high density polyethylene layer 2 and the medium density polyethylene layer were measured. The following evaluations were also carried out. The results are shown in Table 1.

<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.
Device: RIGAKU Corporation, product name: Ultima IV (small angle scattering attachment system)
X-ray incidence direction: normal to the film X-ray wavelength: 0.15418 nm
Optical unit specifications:
1. Optical system selection slit; 0.03 mm (= ^1st slit) for small angle scattering
2. DS: Anti-scattering slit 1.00 mm (= ^2nd slit)
3. Soller slit on the entrance side: 5° flexible optical system used 4. Distance between ^1st and ^2nd slits: 70 mm
^5.2nd . ~ Sample distance: 98 mm
6. Vacuum path length: 100 mm (installed on a dedicated stand in front of the receiving slit box)
7. RS, SS: scattering slit 0.20 mm, receiving slit 0.10 mm
8. Camera length: 285mm
9. Solar slit on the receiving side: 5° flexible optical system used 10. Monochromatization: None (monochromatization on the incident 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 thickness of about 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 a 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 formula (1), and this was substituted into Bragg's formula (2) to calculate the crystal long period (d).
q = 4π sin θ / λ (1)
θ: diffraction angle q: scattering vector magnitude λ: X-ray wavelength 2d sin θ=λ (2)
d: Crystal long period θ: Diffraction angle λ: X-ray wavelength Also, referring to the structural analysis of crystalline polymer materials by scattering method in Nichias Technical Review (2014) No. 2 No. 365, the electron density correlation function γ(r) was calculated by Fourier transforming the SAXS profile I(q) using the following formula (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).

In addition, 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 (manufactured by RIGAKU Corporation). Specifically, air scattering was removed from the SAXS profile I(q) obtained above. Using the obtained values, the above software separated the data into crystalline scattering and amorphous scattering, 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 under the following (analysis conditions).
(Analysis conditions)
Fitting peak shape: split pseudo-Voigt function Crystallite size distribution type: Lorentz model

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

<Tensile modulus>
A test piece of 15 mm x 15 cm was cut out from each stretched polyethylene film. Then, using a tensile tester manufactured by Orientec Co., Ltd., 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 under the conditions of a measurement temperature of 23±2°C, 50±5% RH, and a tensile speed of 5 mm/min. The total value of _T1 and _T2 was calculated from the obtained values.

<Heat shrinkage rate in MD direction of stretched polyethylene film at 100° C.>
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 of 10 cm x 10 cm was cut out from the stretched polyethylene film of each example. The test piece was then heat-treated at 100°C for 15 minutes. At this time, the test piece was heated in a hot air circulation type thermostatic chamber (manufactured by ADVANTEC, product name: DRM620DE) while hanging without applying force. The test piece was then cooled to room temperature, and the length of the test piece was measured. The length of the test piece in the MD direction after the heat treatment was taken as MD ₁₀₀ [cm], and the heat shrinkage rate [%] in the MD direction was calculated by 100 x (10 - MD ₁₀₀ ) / 10. The above measurement was performed three times, and the average value of the obtained measurements was adopted as the heat shrinkage rate of the stretched polyethylene film at 100°C.

<Heat shrinkage rate in MD direction of stretched polyethylene film at 120°C>
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 of 10 cm x 10 cm was cut out from the stretched polyethylene film of each example. The test piece was then heat-treated at 120°C for 15 minutes. At this time, the test piece was heated in a hot air circulation type thermostatic chamber (manufactured by ADVANTEC, product name: DRM620DE) while hanging without applying force. The test piece was then cooled to room temperature, and the length of the test piece was measured. The length of the test piece in the MD direction after the heat treatment was taken as MD ₁₂₀ [cm], and the heat shrinkage rate [%] in the MD direction was calculated by 100 x (10 - MD ₁₂₀ ) / 10. The above measurement was performed three times, and the average value of the obtained measurements was adopted as the heat shrinkage rate of the stretched polyethylene film at 120°C.

<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 the stretched polyethylene films 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 surfaces 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.

<Heat fusion strength>
Two sheets of the 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 two sheets of stretched polyethylene film were then peeled off under conditions of 15 mm width, 90° peeling, a peeling speed of 300 mm/min, and pulling in the MD direction, and the peel strength at this time was recorded as the heat-sealing strength (N/15 mm).

<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 of the stretched polyethylene films of the examples. Then, the piercing strength (N) from the corona-treated surface toward 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.

<Flexibility>
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.).

<Tear strength>
As an index of flexibility, tear strength was measured as follows.
A test piece of 63.5 mm in the MD direction and 50.0 mm in the TD direction was cut out from each stretched polyethylene film. The tear strength (mN) in the MD direction of each test piece was measured 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°.

The flexibility of the stretched polyethylene films was evaluated according to the following criteria.
(standard)
A (good): All of the following (i) to (iii) are satisfied. B (poor): One or more of the following (i) to (iii) are not satisfied. (i) The puncture strength is 4.0 N or more.
(ii) The bending resistance (number of pinholes) is 2,700/ ^m2 or less.
(iii) The tear strength in the MD direction is 100 mN or more.

When the stretched polyethylene film of the embodiment was used, a food packaging film with improved flexibility (performance balance of puncture strength, bending resistance, and tear strength) was obtained.

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

Claims (14)

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 stretched polyethylene film having an amorphous thickness of less than 12.5 nm, as determined from peaks in the MD direction diffraction angle 2θ range of 0.2 to 0.4° by small angle X-ray scattering (SAXS) measurement. 2. The stretched polyethylene film according to claim 1, wherein the stretched polyethylene film has a tensile modulus in the TD direction T2 of 920 MPa or more, as measured using a tensile tester in accordance with JIS K7127:1999 under conditions of a measurement temperature of 23± ₂ °C, a relative humidity of 50±5%, and a tensile speed of 5 mm/min. The stretched polyethylene film according to claim 1 or 2, wherein the medium-density polyethylene layer has a density, measured in accordance with JIS K 7112:1999, of 910 kg/m ³ or more and less than 940 kg/m ³ . The stretched polyethylene film according to any one of claims 1 to 3, 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. The stretched polyethylene film according to any one of claims 1 to 4, wherein the high-density polyethylene layer 1 and the high-density polyethylene layer 2 each have a density, measured in accordance with JIS K 7112:1999, of 940 kg/ ^m3 or more and 970 kg/ ^m3 or less. The stretched polyethylene film according to any one of claims 1 to 5, wherein the haze per sheet of the stretched polyethylene film measured in accordance with JIS K 7136:2000 is 16.0% or less. The stretched polyethylene film according to any one of claims 1 to 6, wherein the sum of the tensile modulus T1 in the MD direction and the tensile modulus 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 1500 MPa or more and 2900 MPa or less. The stretched polyethylene film according to any one of claims 1 to 7, wherein the heat shrinkage rate in the MD direction of the stretched polyethylene film is 6.0% or less when heat-treated at 100°C for 15 minutes in accordance with JIS C2151:2019. The stretched polyethylene film according to any one of claims 1 to 8, wherein at least one surface of the stretched polyethylene film is a corona-treated surface. At least one surface of the stretched polyethylene film is a non-corona treated surface,
The stretched polyethylene film according to any one of claims 1 to 9, wherein the heat fusion strength when the non-corona treated surface of the stretched polyethylene film is bonded to the non-corona treated surface and heat sealed at 140°C is 4.0 N/15 mm or less. The stretched polyethylene film according to any one of claims 1 to 10, wherein the total thickness of the stretched polyethylene film is 10 μm or more and 100 μm or less. The stretched polyethylene film according to any one of claims 1 to 11, which is a film for food packaging. A packaging material using the stretched polyethylene film according to any one of claims 1 to 12. A packaging material according to claim 13;
and a food product within the packaging material.

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