WO2011129167A1 - 表面保護フィルム - Google Patents
表面保護フィルム Download PDFInfo
- Publication number
- WO2011129167A1 WO2011129167A1 PCT/JP2011/055627 JP2011055627W WO2011129167A1 WO 2011129167 A1 WO2011129167 A1 WO 2011129167A1 JP 2011055627 W JP2011055627 W JP 2011055627W WO 2011129167 A1 WO2011129167 A1 WO 2011129167A1
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- WIPO (PCT)
- Prior art keywords
- layer
- resin
- adherend
- ethylene
- film
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C09J123/0815—Copolymers of ethene with aliphatic 1-olefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/308—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising acrylic (co)polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C09J123/0869—Acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/29—Laminated material
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2457/00—Electrical equipment
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
- C09J2301/122—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/312—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
- C09J2423/04—Presence of homo or copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
- C09J2423/04—Presence of homo or copolymers of ethene
- C09J2423/046—Presence of homo or copolymers of ethene in the substrate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
- C09J2423/10—Presence of homo or copolymers of propene
- C09J2423/106—Presence of homo or copolymers of propene in the substrate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
Definitions
- the present invention relates to a surface protective film that is temporarily attached to the surface of various optical films such as polarizing plates and retardation plates mainly used in the field of optics, and in particular, due to fish eyes and wound wrinkles of the surface protective film.
- the present invention relates to a surface protective film having characteristics that do not cause dent defects such as dents and deformations on the adherend and does not contaminate the adherend surface.
- the surface protection film is required to have a light adhesion that can be easily peeled off when the surface protection function is completed, while maintaining an adhesive function that can withstand harsh usage conditions. In other words, it is required not to leave a trace of the surface protective film on the adherend.
- it does not cause dent defects such as dents and deformations on the adherend due to convex defects such as fish eyes in the surface protection film and winding wrinkles It is strictly required. In recent years, this requirement has become more and more severe. Even when the surface protective film is bonded to the adherend, it is wound into a roll and stored as a wound body for a long period of time. Protruding part defects due to extremely small fish eyes or dent defects such as dents and deformation due to very small winding wrinkles may occur due to load being received, and it is required that such defects do not go away. Yes.
- the surface protective film is usually provided in the form of a roll, but it is excellent in slipping property and blocking resistance between the adhesive layer and the back surface layer (easy to unwind), and the workability when sticking to the adherend is stable. It is a basic requirement to have excellent workability.
- the surface protective film needs to satisfy both the active and inactive contradictory functions as material characteristics at the same time, and various proposals have been made to satisfy these required characteristics.
- Patent Documents 1, 2, and 3 Many proposals have been made to use an ethylene / ⁇ -olefin copolymer for the adhesive layer as a means for preventing an increase in adhesive force during high-temperature processing of the surface protective film.
- Patent Document 4 As a method for improving the ease of unwinding of the surface protective film, it has been proposed to add inorganic particles to the thermoplastic resin constituting the base material layer (Patent Document 4).
- Patent Document 5 There is no one that satisfies a plurality of intersecting characteristics at the same time, and the present inventors have proposed to satisfy the plurality of intersecting characteristics at the same time.
- Patent Document 7 a proposal using a polyethylene-based resin for the base layer in order to eliminate the dents (dents) on the adherend due to the convex defects such as fish eye, which have been increasingly demanded recently (patent document) 6) Or a proposal using a polypropylene-based resin (Patent Document 7) has been made, but it has not yet reached a level that is sufficiently satisfied with respect to elimination of dents on the adherend due to fine fish eyes or the like. .
- Patent Document 6 although it is proposed to use low density polyethylene or the like for the base material layer, the fish eye itself cannot be completely eliminated, and the retardation plate has a very smooth surface.
- the surface protective film and the adherend are pasted together and stored for a long time as a roll-shaped scroll. Since stress concentration occurs in the bulge (convex) portion of the protective film due to the fish eye, this bulge causes a dent defect in the adherend, and it is still possible to completely eliminate dents due to the fish eye etc. of the adherend. It was difficult.
- Patent Document 7 it has been proposed to use a polypropylene resin for the base material layer to reduce the fish eye itself, but when a polypropylene resin is used for the base material layer, the number of fish eyes can be reduced. Since the base material layer is hard and inferior in cushioning properties, the presence of fish eye defects tends to make the dent on the adherend more severe than when a polyethylene resin is used.
- the present invention is required to have a high quality, such as not causing dents or deformations in the adherend due to defects such as minute fish eyes or winding wrinkles, in a laminated structure comprising an adhesive layer, an intermediate layer and a back layer.
- Adhesive strength is not increased with respect to optical films such as polarizing plates and retardation plates, and the adherend is contaminated, and dent defects such as dents and deformation are caused in the adherend. It is intended to provide a surface protective film that does not have any.
- the adherend does not cause dents or contamination such as dents due to various wrinkles of the fish eye or film
- the present invention is based on the background of the above prior art, and is slippery and blocking. In addition to handling characteristics such as easy to handle and waist, it satisfies basic adhesive properties and has little increase in adhesive strength. It is an object of the present invention to provide a surface protective film that is less likely to be dented or deformed to an adherend due to eye or the like or film wrinkles.
- the surface protective film of the present invention comprises a three-layer laminated form of an adhesive layer, an intermediate layer and a back layer
- the adhesive layer comprises an ethylene / ⁇ -olefin copolymer, an ethylene / methyl methacrylate copolymer, or
- the intermediate layer is mainly composed of a polyethylene resin having a density of 0.870 to 0.935 g / cm 3, an ethylene / methyl methacrylate copolymer, or a mixture of these
- the back layer Is composed of a polypropylene resin and low-density polyethylene, and the surface roughness of the back layer is 0.6 ⁇ m or more as arithmetic average roughness (Ra) and 4 ⁇ m or more as 10-point average roughness (Rz). It is characterized by.
- the polypropylene resin constituting the back layer of the surface protective film of the present invention has a melt flow rate in the range of 5 to 50 g / 10 min at 230 ° C. and a load of 2.16 kg / cm 2 ,
- the melt flow rate of low density polyethylene at 190 ° C. and a load of 2.16 kg / cm 2 is 0.5 to 5 g / 10 min.
- the surface protective film of the present invention has a three-layer laminated form of an adhesive layer, an intermediate layer, and a back layer
- the intermediate layer is a polyethylene resin having a density of 0.870 to 0.935 g / cm 3
- ethylene -It consists of a mixed resin composition of a methyl methacrylate copolymer, or one of these mixtures, and an adhesive layer constituting resin and a back layer constituting resin.
- the above-described problems can be solved, and the film can be easily rewound when unrolled with the adherend, and there is a waist, which is handled even in the pasting process with the adherend. It is easy and excellent in workability, and in particular, dents and contamination such as dents and deformations occur on the adherend due to fish eyes and various wrinkles of the film required for optical films such as polarizing plates and retardation plates. It is possible to provide a surface protective film having no reproducibility with good reproducibility.
- the present invention will be described in detail below.
- the present invention is caused by the above problems, that is, adhesive strength, various processing characteristics, handling properties represented by blocking properties (surface properties), especially convex defects such as fish eyes and various wrinkles of the film.
- Specific adhesive layer and intermediate layer that alleviate stress concentration on convex parts due to bulging of fish eyes, etc., by intensively studying surface protection films that do not cause dent defects such as dents and deformation, and contamination on the adherend
- the present inventors have investigated that such a problem can be solved at once by adopting a laminated form composed of a back layer.
- the requirements for the adhesive layer of the present invention are as follows.
- the pressure-sensitive adhesive layer of the present invention is made of an ethylene / ⁇ -olefin copolymer, an ethylene / methyl methacrylate copolymer, or a mixture thereof.
- the ethylene / ⁇ -olefin copolymer is a so-called linear low density polyethylene or ultra-low density polyethylene, and the type of ⁇ -olefin as a comonomer is not particularly limited, butene-1, hexene-1, 4-methyl pentene-1, octene-1, etc. can be mentioned.
- the density of the ethylene / ⁇ -olefin copolymer can be in the range of 0.870 to 0.935 g / cm 3 , and the adhesive strength is particularly high even when subjected to a high temperature treatment of 120 ° C. or higher.
- the ethylene / ⁇ -olefin copolymer has a density of 0.910 to 0.935 g / cm 3 and a melting point main peak of 100 to 130 ° C. Then, it is particularly preferable because the adhesion force to the adherend is stabilized without contaminating the adherend surface, and excellent adhesive properties such that the adhesive force is hardly increased even when subjected to high temperature treatment are obtained.
- the density and melting point of such an ethylene / ⁇ -olefin copolymer are determined by the state of short-chain branching of the ⁇ -olefin and the resulting crystal state.
- the structure factor of ethylene / ⁇ -olefin copolymer includes short chain branching species, short chain branching degree and composition distribution in addition to its average molecular weight and molecular weight distribution, but the requirements for density and melting point are comonomer amount of 10 mol. % Can be obtained.
- Such an ethylene / ⁇ -olefin copolymer may show a plurality of melting point peaks, but in the present invention, it refers to the main peak of the melting point determined from a differential scanning calorimetry (DSC) curve using a differential scanning calorimeter.
- the ethylene / ⁇ -olefin copolymer is obtained by using a polymerization method using a single-site catalyst (Kaminsky catalyst, metallocene catalyst) in addition to the conventional polymerization method using a multi-site catalyst, both of which are useful in the present invention. can do.
- Other components may include other polyolefins, olefin copolymer polymers, aliphatic compounds, or cyclic compounds, but are preferably limited to the minimum necessary amount. If it is added more than necessary, it will cause contamination of the adherend.
- the ethylene / methyl methacrylate copolymer which is another requirement of the present invention, is a resin obtained by copolymerizing ethylene with methyl methacrylate (hereinafter abbreviated as MMA).
- MMA copolymer a resin obtained by copolymerizing ethylene with methyl methacrylate (hereinafter abbreviated as MMA).
- a copolymerization ratio of 5% by weight to about 40% by weight is available, but the adhesive layer resin preferably has a MMA copolymerization ratio in the range of 5% by weight to 20% by weight. .
- those having a MMA copolymerization ratio in the range of 10 to 15% by weight are more preferable.
- the MMA copolymerization ratio is less than 5% by weight, it is difficult to obtain a desired adhesive strength.
- the MMA copolymerization ratio exceeds 20% by weight the melting point becomes too low and the heat resistance is inferior.
- ethylene / ⁇ -olefin copolymer and ethylene / methyl methacrylate copolymer can each independently constitute an adhesive layer, or can be appropriately adjusted to suit the desired adhesive strength at an arbitrary ratio. It is.
- an antioxidant of 500 to 3 is used.
- the addition of 1,000 ppm is a preferable method, but it is preferable to limit the amount to the minimum required amount because there is a possibility of contaminating the adherend if it is added too much.
- Antioxidants include phenol-based, aromatic amine-based, thioether-based, phosphorus-based and the like, and it is preferable to use two or more types in combination in order to increase the effect with a small amount. For example, the combined use of phenol and phosphorus is a preferred method.
- a tackifier such as a terpene compound may be added to the adhesive layer.
- a tackifier such as a terpene compound
- it is applied to an adherend such as a polarizing plate or a retardation plate having a smooth surface.
- an appropriate adhesive property can be imparted without using a tackifier.
- tackifiers include polyterpenes having structural units such as ⁇ -pinene, ⁇ -pinene, and dipentene, hydrogenated products (hydrogenated terpene resins), terpene styrene resins, terpene phenol resins as such modified products,
- rosins include rosin, polymerized rosin, hydrogenated rosin, rosin-modified products, and derivatives of rosin or hydrogenated rosin glycerin ester, pentaerythritol ester, and the like.
- the surface roughness of the pressure-sensitive adhesive layer of the present invention formed by such a configuration is 0.2 ⁇ m or less as arithmetic average roughness (Ra) and 2 ⁇ m or less as ten-point average roughness (Rz). It is preferable to have a smoothed surface shape. By smoothing the pressure-sensitive adhesive layer, it is possible to bond to an adherend with good adhesion without being invaded by bubbles when bonded to a smooth optical film such as a polarizing plate or a retardation plate. it can.
- the adhesive layer has a rough adhesive layer with a (Ra) of 0.2 [mu] m and (Rz) greater than 2 [mu] m, the adhesion to the adherend is poor, and the adherend is not easily lifted or peeled off during processing or storage. This is undesirable because it causes problems.
- the intermediate layer of the surface protective film of the present invention is mainly composed of a polyethylene resin having a density of 0.870 to 0.935 g / cm 3, an ethylene / methyl methacrylate copolymer, or a mixture thereof.
- polyethylene resins include high pressure method low density polyethylene, linear low density polyethylene, and ultra low density polyethylene.
- the intermediate layer is made of a flexible resin because it relaxes stress concentration on the adherend of bulges (convex portions) such as fish eyes, which will be described later, and provides cushioning properties.
- the flexural modulus is preferably 500 MPa or less, more preferably 300 MPa or less.
- the flexural modulus By setting the flexural modulus to 500 MPa or less, it is possible to relieve stress on the bulging adherend such as fish eyes and to reduce damage to the dent on the adherend. Further, by setting the flexural modulus to 20 MPa or more, it is possible to obtain a firm and easy-to-handle surface protective film in combination with the resin structure of the back layer of the present invention described later.
- high-pressure low-density polyethylene having a density of 0.910 to 0.935 g / cm 3 is preferable because it can reduce the fish eye of the resin itself and has excellent cushioning properties.
- linear low-density polyethylene having a density of 0.870 to 0.935 g / cm 3 is more preferable because it makes the intermediate layer flexible, has excellent spreadability, and can form a thin film at high speed.
- so-called ultra-low density polyethylene having a density of 0.870 to 0.91 g / cm 3 can be used particularly preferably because the intermediate layer is made more flexible and has excellent cushioning properties.
- the density is less than 0.870 g / cm 3 , it is too soft, and it is not desirable because it is difficult to handle even if combined with the resin composition of the back layer described later.
- ultra-low density polyethylene polyethylene plastomers using hexene-1 or octene-1 as a comonomer, “Kernel” manufactured by Nippon Polyethylene Co., Ltd., “Excellen VL” manufactured by Sumitomo Chemical Co., Ltd., Tosoh Corporation ) “LUMITAC”, “Affinity” manufactured by Dow Chemical Co., Ltd., “Nack Flex” and the like.
- the ethylene / methyl methacrylate copolymer that can be used for the intermediate layer may be the same as or different from the above-mentioned adhesive layer-constituting resin.
- Such an ethylene / methyl methacrylate copolymer is preferable because it has a flexibility equal to or higher than that of the polyethylene resin.
- a resin having a bending elastic modulus of 100 MPa or less can be easily obtained.
- the intermediate layer includes a polyethylene-based resin having a density of 0.870 to 0.935 g / cm 3, an ethylene / methyl methacrylate copolymer, or a mixture thereof, and an adhesive layer constituting resin and You may add and mix the below-mentioned back surface layer resin.
- the non-uniform thickness of the edge is slit and removed by a slitting process or the like, but using this part for the intermediate layer can reduce the amount of raw material used. This is an economically preferable method.
- the addition / mixing amount to the intermediate layer is preferably less than 30% by weight of the back layer constituting resin described later.
- the content of the back layer resin mainly composed of such a polypropylene resin is increased, it becomes difficult to obtain the flexibility of the intermediate layer which is the gist of the present invention.
- the intermediate layer of the present invention is preferably 60% by weight or more, more preferably one kind of polyethylene resin having a density of 0.870 to 0.935 g / cm 3 , ethylene / methyl methacrylate copolymer, or a mixture thereof. Is composed of 70% by weight or more, so that the intermediate layer can be softened and the stress concentration of convex defects such as fish eyes can be alleviated.
- fillers such as talc, stearamide, calcium stearate, lubricants, antioxidants, ultraviolet absorbers, pigments, antistatic agents, nucleating agents, and the like may be appropriately added. Moreover, you may add these individually or in combination of 2 or more types.
- the back layer of the surface protective film of the present invention is composed of a polypropylene resin and low density polyethylene.
- the polypropylene resin include homopolypropylene, a random or block copolymer of propylene and ethylene, and a copolymer of propylene, ethylene, and butene.
- the surface of the back layer which is a constituent requirement of the present invention, can be used. For the purpose of roughening, it is preferably used as a random copolymer of propylene and ethylene alone or as a mixture of homopolypropylene.
- Such a random copolymer of propylene and ethylene preferably has an ethylene content in the range of 1 to 7% by weight from the viewpoint of heat resistance, slipperiness and film handling properties.
- the melt flow rate (hereinafter abbreviated as MFR) at 230 ° C. under a load of 2.16 kg / cm 2 is preferably in the range of 5 to 50 g / 10 min.
- MFR melt flow rate
- those having MFR of 10 to 40 g / 10 min are more preferred because they can be extruded at low temperature and can easily roughen the back layer when combined with low density polyethylene described later.
- the MFR of the mixed resin when two or more types of polypropylene resins are used represents the measured value, if any, but if the MFR value as a mixed resin has not been evaluated, the MFR of the single resin is used. A value obtained by dividing the logarithm of each by the resin ratio is used.
- the low density polyethylene to be blended is preferably a low density polyethylene having a density range of 0.910 to 0.935 g / cm 3 .
- the density exceeds 0.935 g / cm 3 , the resin is liable to fall off during rubbing with a metal roll or a rubber roll, which tends to cause white powder.
- the low-density polyethylene may be the same as the low-density polyethylene used for the intermediate layer.
- the temperature is 190 ° C. and the load is 2.16 kg / cm 2.
- the MFR is preferably as high as 0.5 to 5 g / 10 min, and the difference between the MFR at 190 ° C. of the low-density polyethylene and the MFR at 230 ° C. of the polypropylene resin is larger (for example, the difference is 10 g / 10 minutes or more, preferably 20 g / 10 minutes or more), which is more preferable because the roughening effect is remarkably exhibited.
- the blending ratio (% by weight) of the polypropylene resin in the back layer and the low density polyethylene is selected in the range of 70:30 to 95: 5 in order to obtain the desired surface roughness.
- the surface roughness of the back layer of the present invention formed by such a configuration is 0.6 ⁇ m or more in arithmetic average roughness (Ra) and 4 ⁇ m or more in ten-point average roughness (Rz). It has a roughened surface shape.
- the back layer can be used to increase stress concentration on the adherend due to bulging by fish eyes, which is the object of the present invention. It is possible to disperse the stress by roughening the surface, relax the stress concentration by utilizing the cushioning property of the intermediate layer, and eliminate the dent on the adherend.
- the surface condition related to slipping and blocking is determined by the polymer constituent requirements. In general, fine particles of inorganic compounds are added to develop slipperiness. However, in the present invention, good slipperiness and blocking properties can be expressed without blending such fine particles of inorganic compounds. It is possible to prevent the adherend from being damaged by the fine particles of the compound.
- the surface protective film of the present invention has a rough surface state in which the back layer has an arithmetic average roughness (Ra) of 0.6 ⁇ m or more and a 10-point average roughness (Rz) of 4 ⁇ m.
- Ra arithmetic average roughness
- Rz 10-point average roughness
- the film By forming a structure having a smooth surface shape with an arithmetic average roughness of 0.2 ⁇ m or less and a ten-point average roughness (Rz) of 2 ⁇ m or less, the film must satisfy stable adhesive force and excellent film handling function at the same time. Can do.
- Such surface roughness can be obtained by analyzing a roughness profile (roughness curve) measured by a commonly used surface shape measuring instrument.
- the method for producing the surface protective film of the present invention is not particularly limited.
- the adhesive layer resin an ethylene / ⁇ -olefin copolymer, an ethylene / methyl methacrylate copolymer, or a mixed resin thereof is used as an intermediate layer resin.
- a back layer resin a polyethylene resin having a density of 0.870 to 0.935 g / cm 3 or an ethylene / methyl methacrylate copolymer, or a mixed resin thereof is used as a back layer resin.
- Each of the resin compositions is melt-extruded from individual extruders, laminated and integrated in a die, and so-called three-layer coextrusion is performed so that the adhesive layer, the intermediate layer, and the back layer are laminated and integrated, and then rolled.
- the method for producing the surface protective film by winding the film on the surface, the adhesive layer, the intermediate layer, and the back layer are melt-pressed individually. After, by laminating method, the adhesive layer, an intermediate layer, and a method in which the back layer is laminated and integrated.
- the melt coextrusion method by the T-die method is preferable from the viewpoint of quality and economy.
- the thickness of the surface protective film of the present invention varies depending on the thickness of the adherend and the required quality level of the adherend, but can generally be appropriately selected within the range of 20 to 100 ⁇ m from the viewpoint of moldability and ease of use. The range of 20 to 50 ⁇ m is particularly preferable.
- each of the adhesive layer, the intermediate layer and the back layer may be appropriately adjusted according to the required level as described above.
- the adhesive layer, intermediate layer The thickness ratio (%) of the layer and the back layer is preferably 15 to 40:81 to 45: 4 to 15 respectively.
- the surface roughness was measured in the lateral direction of the film (TD direction of the film) in accordance with JIS B0601-1994 using a fully automatic fine shape measuring machine (SURFCORDER ET4000A) manufactured by Kosaka Laboratory.
- the measurement length was 2 mm, the measurement was performed 20 times at a pitch of 10 ⁇ m in the longitudinal direction (machine direction), and three-dimensional analysis was performed to obtain the arithmetic average roughness (Ra) and the ten-point average roughness (Rz), respectively (unit: ⁇ m).
- a stylus tip radius of 2.0 ⁇ m and apex angle of 60 ° were used, and measurement was performed at a measuring force of 10 ⁇ N and a cutoff of 0.8 mm.
- sample sample Roll press machine Yamada Seiki Co., Ltd.
- sample samples of Examples and Comparative Examples stored and adjusted under conditions of a temperature of 23 ° C. and a humidity of 50% RH for 24 hours.
- the film was pasted at a pasting pressure of 9,100 N / m and a pasting speed of 300 cm / min. Thereafter, the sample was stored for 24 hours under conditions of a temperature of 23 ° C. and a humidity of 50% RH, and then used for each measurement and evaluation.
- Example 1 The constituent resin of each layer was prepared as follows.
- As the adhesive layer resin an ethylene-hexene-1 copolymer (linear low density) having a density of 0.922 g / cm 3 containing 1000 ppm of a phosphorus-based antioxidant, a melting point of 116 ° C., and an MFR of 5.0 g / 10 min at 190 ° C.
- the back layer resin was MFR 35 g / 230 ° C. at 230 ° C. 10 min, an ethylene content of 5 wt% of an ethylene - propylene random copolymer 80 wt% and 190 ° C.
- the film wound up in a roll shape was subjected to a slitting machine to finish a size of 1600 mm in width and 7,000 m in length, and a film sample wound up in a roll shape was obtained.
- a product with a predetermined width is obtained with a slitting machine, it is not necessary to perform a release treatment or the like, and it can be easily sent out (unwinded) to the slitting machine without any resistance, and blocking is completely recognized. There wasn't. When blocking occurs, when the adhesive layer and the back surface layer are peeled off, a sound is heard, but it was confirmed that there was no peeling sound and the wire was unrolled very smoothly.
- the adhesive layer had a surface roughness (Ra) of 0.13 ⁇ m and (Rz) of 1.4 ⁇ m.
- the surface roughness (Ra) was 1.2 ⁇ m and (Rz) was 8.4 ⁇ m, and the back layer side had an uneven surface.
- the film sample was cut to a length of 1 m over the entire width, and the fish eye was visually checked and checked. As a result, a fish eye having a major axis of about 100 ⁇ m or more that could be visually recognized was not detected and was 0 / m 2 .
- the sample sample was evaluated at the same time as Comparative Example 1 described later, and the adhesive property was evaluated using a retardation film made of a cyclic olefin having a smooth surface thickness of 100 ⁇ m.
- the adhesion to the adherend was very good.
- the adhesive strength was 0.08 N / 50 mm. After peeling the film, the surface of the adherend was observed, but no contamination was observed.
- the number of fish eyes was 0 / m 2 .
- the number of fish eyes of 100 ⁇ m or more was also 0 / m 2 ), and when transferability of fish eyes to the adherend (depression on the adherend was evaluated) was evaluated, there was no dent on the adherend, and the back surface Although the layer was uneven, transfer of the unevenness was not recognized.
- Example 1 The same ethylene / hexene-1 copolymer (linear low density polyethylene) as in Example 1 was used as the adhesive layer resin, and the density was 0.964 g / cm 3 , melting point 135 ° C., 190 ° C. as the intermediate layer resin.
- the back layer resin has a melting point of 163 ° C., MFR 7.5 g / 10 min at 230 ° C. and 98% by weight homopolypropylene at 190 ° C. MFR 2 g / 10 min, density 0.92 g / except that those were uniformly mixed resin composition consisting of low density polyethylene 2 wt% of cm 3 by a Henschel mixer, in the same manner as in example 1 T-die type 3-layer composite film-forming machine Used, was formed a 3-layer laminated film of the film thickness of 35 [mu] m.
- the obtained film had a haze value of 11, without blocking, and could be easily rewound.
- the adhesive layer had a surface roughness (Ra) of 0.13 ⁇ m and (Rz) of 0.51 ⁇ m, and the surface roughness of the back layer (Ra) of 0.14 ⁇ m and (Rz) of 1.3 ⁇ m.
- the adhesive layer and the back layer were smooth films.
- the number of fish eyes of 0.05 mm 2 or more was 7 / m 2 , but the number of visible eyes having a major axis of about 100 ⁇ m or more was 280 / m 2 .
- Example 2 In the evaluation simultaneously with Example 1 described above, a fish eye part having a size of 0.05 mm 2 was marked, and the transferability of the fish eye in the part was evaluated.
- the fish eye part In the comparative example, the fish eye part was the adherend. The dent was generated.
- Example 2 The constituent resin of each layer was prepared as follows.
- As the adhesive layer resin an ethylene-hexene-1 copolymer (linear low density) having a density of 0.922 g / cm 3 containing 1000 ppm of a phosphorus-based antioxidant, a melting point of 116 ° C., and an MFR of 5.0 g / 10 min at 190 ° C. Polyethylene) 40% by weight, phenolic antioxidant 1200ppm in density 0.875, melting point 71 ° C., 190 ° C.
- Extrusion was performed at a temperature of 210 ° C., a three-layer laminated film having a film thickness of 30 ⁇ m was formed, and once wound into a roll.
- the MFR of the polypropylene-based mixed resin for the back layer is 16.2 g / 10 min by the above-described calculation method.
- the film wound up in a roll shape was subjected to a slitting machine, finished to a size of 1300 mm in width and 3,000 m in length, and a film sample wound up in a roll shape was obtained.
- the adhesive layer had a surface roughness (Ra) of 0.08 ⁇ m and (Rz) of 0.43 ⁇ m.
- the surface roughness (Ra) was 0.71 ⁇ m
- (Rz) was 5.3 ⁇ m
- the back layer side had an uneven surface.
- the film sample was cut from the film sample to a length of 1 m and the fish eyes were visually checked.
- the number of fish eyes of 0.05 mm 2 size or larger was 0 / m 2 .
- the size of the major axis of 100 ⁇ m or more that can be visually recognized was counted, one was found in 1 m 2 .
- the sample sample was evaluated at the same time as Comparative Example 2 described later, and the adhesive property was evaluated using a thin polarizing plate having a surface smoothness of 100 ⁇ m.
- the adhesion to the adherend was very good (adhesion)
- the force was 0.09 N / 50 mm), and after peeling the film, the surface of the adherend was observed, but no contamination was observed.
- Example 3 As the adhesive layer resin, instead of 100% by weight of the ethylene / hexene-1 copolymer (linear low density polyethylene) of Example 1, a density of 0.93 g / cm 3 , MMA 10% by weight of MFR 7 g / 10 min at 190 ° C. Using 60% by weight of the copolymerized ethylene / methyl methacrylate copolymer and 40% by weight of the ethylene / hexene-1 copolymer of Example 1, the same ethylene. A three-layer laminated film having a film thickness of 35 ⁇ m was formed in the same manner as in Example 1 except that a methyl methacrylate copolymer was used, and the film was once wound into a roll.
- the film wound up in a roll shape was subjected to a slitting machine to finish a size of 1600 mm in width and 7,000 m in length, and a film sample wound up in a roll shape was obtained.
- the film unwinding characteristics of the roll sample could be easily unwound without applying any particular tension.
- the adhesive layer had a surface roughness (Ra) of 0.12 ⁇ m and (Rz) of 1.3 ⁇ m.
- the surface roughness (Ra) was 1.1 ⁇ m
- (Rz) was 8.1 ⁇ m
- the back layer side had an uneven surface.
- the film sample was cut to a length of 1 m over the entire width, and the fish eye was visually checked and checked. As a result, a fish eye having a major axis of about 100 ⁇ m or more that could be visually recognized was not detected and was 0 / m 2 .
- the sample film was evaluated using the same retardation film made of a cyclic olefin having a thickness of 100 ⁇ m as in Example 2 and the adhesive properties were evaluated.
- the adhesion to the adherend was very good, and the adhesive strength was It was 0.09 N / 50 mm, and after peeling this film, the surface of the adherend was observed, but no contamination was observed.
- the fish eye was not visually recognized as in Example 1.
- the transferability of fish eye to the adherend depression on the adherend was evaluated.
- transfer to the adherend due to unevenness of the back layer was not observed.
- Example 4 Except for using 100% by weight of ethylene / methyl methacrylate copolymer copolymerized by 10% by weight of MMA at 190 ° C. under MFR of 7 g / 10 min at 190 ° C., the same as in Example 1, A three-layer laminated film having a film thickness of 35 ⁇ m, a width of 1600 mm, and a length of 7,000 m was finished. It should be noted that when a product having a predetermined width was obtained, it could be easily sent out (wound out) to the slitting machine without any resistance, and no blocking was observed.
- the haze value of the obtained film was 51, and when the surface roughness was measured, the adhesive layer had a surface roughness (Ra) of 0.14 ⁇ m and (Rz) of 1.5 ⁇ m.
- the surface roughness (Ra) was 1.2 ⁇ m and (Rz) was 8.4 ⁇ m, and the back layer side had an uneven surface.
- the film sample was cut to a length of 1 m over the entire width, and the fish eye was visually checked and checked. As a result, a fish eye having a major axis of about 100 ⁇ m or more that could be visually recognized was not detected and was 0 / m 2 .
- the adhesive property was evaluated using a retardation film made of a cyclic olefin having a thickness of 100 ⁇ m as in Example 1, the adhesive strength was 0.12 N / 50 mm, and the film was peeled off. After that, the surface of the adherend was observed, but no contamination was observed.
- the fish eye could not be confirmed by visual observation as in Example 1. Therefore, when the sample eye was used as it was and the fish eye transferability was evaluated, there was no dent on the adherend, and the back layer was Although the surface was uneven, no transfer of the unevenness was observed.
- Comparative Example 2 The constituent resin of each layer was prepared as follows.
- the adhesive layer resin the same ethylene-hexene-1 copolymer (linear low density polyethylene) as in Comparative Example 1 was used, and as the intermediate layer resin, the density was 0.964 g / cm 3 , the melting point was 134 ° C., and 190 ° C.
- a high-density polyethylene having a lower MFR of 7.5 g / 10 minutes is used as a back layer resin, MFR 5.5 g / 10 minutes at 190 ° C., 94% by weight of low-density polyethylene having a density of 0.923 g / cm 3 , MFR 2 g / 10 minutes at 190 ° C.
- the obtained film had a haze value of 12, without blocking, and could be easily rewound. Further, when the surface roughness was measured, the adhesive layer had a surface roughness (Ra) of 0.09 ⁇ m and (Rz) of 0.48 ⁇ m, and the surface roughness of the back layer (Ra) of 0.12 ⁇ m and (Rz) of 2.4 ⁇ m.
- the adhesive layer and the back layer were relatively smooth films.
- fish eyes were evaluated in the same manner as in Example 2, fish eyes having a size of 0.05 mm 2 to 0.1 mm 2 were 13 / m 2 , and those having a major axis of about 100 ⁇ m or larger were 220 / m 2 .
- the fish eye transferability was evaluated in the same evaluation as in Example 2 described above. As a result, the fish eye portion of the comparative example 2 caused a dent in the adherend.
- Example 5 is the same as Example 1 except that ultra-low density polyethylene having the same density of 0.875 g / cm 3 and MFR of 3 g / 10 min as that used in the adhesive layer of Example 2 is used as the intermediate layer resin. A film was obtained.
- the low-density polyethylene (butene-1 copolymer) having a density of 0.934 g / cm 3 and MFR of 5 g / 10 min was used in the same manner as in Example 1 except that linear low low-density polyethylene (butene-1 copolymer) was used. A film was obtained.
- a resin composition comprising 60% by weight of a high-pressure low-density polyethylene having a density of 0.923 g / cm 3 and MFR of 10 g / 10 minutes at 190 ° C. and 40% by weight of the back layer constituting resin composition of Example 1.
- a film of Example 7 was obtained in the same manner as in Example 1 except that the product was uniformly mixed with a Henschel mixer.
- Example 7 The fish eye transferability was evaluated using the same adherend as in Example 1.
- the sample films of Examples 5 and 6 showed good fisheye transferability.
- Example 7 a slight fisheye dent was observed.
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Abstract
Description
本発明は、前記課題、つまり、粘着力や多種多様な加工特性、ブロッキング性で代表されるハンドリング性(表面特性)をはじめ、特にフィッシュアイ等の凸部欠点やフィルムの各種シワ等が起因で被着体に凹みや変形等の打痕欠点や汚染などが生じることのない表面保護フィルムについて、鋭意検討し、フィッシュアイ等の膨らみによる凸部の応力集中を緩和させる特定な粘着層、中間層、背面層からなる積層形態にすることで、かかる課題を一挙に解決することを究明したものである。
酸化防止剤としては、フェノール系、芳香族アミン系、チオエーテル系、リン系などがあり、少量配合で効果を高めるため、2種以上のものを併用するのが好ましい。例えば、フェノール系とリン系の併用は好ましい方法である。
かかる場合の中間層への添加・混合量としては、後述の背面層構成樹脂30重量%未満までが好ましい。かかるポリプロピレン系樹脂を主体とした背面層樹脂の含有量が多くなると、本発明の骨子である中間層の柔軟性が得られ難くなる。
表面粗さは、(株)小坂研究所製の全自動微細形状測定機(SURFCORDER ET4000A)を用い、JIS B0601-1994に準拠し、フィルム横方向(フィルムのTD方向)に測定長さ2mmで、長手方向(マシン方向)に10μmピッチで20回測定して3次元解析し、算術平均粗さ(Ra)及び、十点平均粗さ(Rz)をそれぞれ求めた(単位はμm)。尚、触針先端半径2.0μm、頂角60°のダイヤモンド針を使用、測定力10μN、カットオフ0.8mmで測定した。
温度23℃、湿度50%RHの条件下で24時間、保管・調整した実施例及び比較例の試料サンプルを被着体に、ロールプレス機((株)安田精機製作所製特殊圧着ローラ)を用い、貼込圧力9,100N/m、貼込速度300cm/分で貼り付けた。しかる後、温度23℃、湿度50%RH条件下で24時間保管した後、各測定と評価に用いた。
引張試験機((株)オリエンテック“テンシロン”万能試験機)を用い、引張速度300mm/分、剥離角度180°にて粘着力を測定した。
被着体と試料サンプルの密着状態を肉眼観察し、次の判定を行った。
B:ごく一部が密着不良で試料フィルムが一部(面積比30%以内)浮いている
C:面積比70%以上の部分でフィルムが被着体から浮いている。
被着体より試料フィルムを剥がした後、暗室内で被着体表面にスポット光を当てて、表面の汚染状態を肉眼観察し、次の判定を行った。
B:軽度の汚染がある
C:汚染している。
予め試料サンプルのフィッシュアイ欠点を国立印刷製造のきょう雑物測定図表と対比し、0.05mm2~0.1mm2サイズのフィッシュアイ欠点部を選別し、該欠点を有する部分を含む試料サンプルを被着体と貼り合わせた後、両側を平滑なポリカーボネート板(板厚み2mm)で挟み込み、荷重1.3kg/cm2を負荷し、60℃熱風オーブン中で3日間保管した後、室温に戻し、その後、被着体より試料フィルムを剥がした後、被着体がフィッシュアイによりへこみが生じていないか判定した。尚、目視にてフィッシュアイ欠点部が全く見つけられなかったサンプルにおいては、試料サンプルをそのまま使用した。
B:僅かにフィッシュアイによるへこみが認められる
C:フィッシュアイによるへこみが明らかに認められる。
(株)東洋精機製作所製メルトインデックサを用い、JIS K7210-1997に準拠し、ポリプロピレン系樹脂の場合は温度230℃、荷重2.16kg/cm2で、ポリエチレン系樹脂及びエチレン・メチルメタクリレートの場合は温度190℃、荷重2.16kg/cm2で測定した。単位はいずれもg/10分である。
各層の構成樹脂を次のように準備した。
粘着層樹脂として、リン系酸化防止剤1000ppmを含有する密度0.922g/cm3、融点116℃、190℃下MFR5.0g/10分のエチレン・ヘキセン-1共重合体(直鎖状低密度ポリエチレン)を用い、中間層樹脂として、密度0.923g/cm3、190℃下MFR10g/10分の高圧法低密度ポリエチレン91重量%に粘着層樹脂6.6重量%及び後述の背面層構成樹脂組成物2.4重量%からなる樹脂組成物(耳部を回収することを想定した組成物とした)をヘンシェルミキサにて均一に混合したものを用い、背面層樹脂として、230℃下MFR35g/10分、エチレン含有量5重量%のエチレン-プロピレンランダム共重合体80重量%と190℃下MFR2g/10分、密度0.92g/cm3の低密度ポリエチレン20重量%からなる樹脂組成物をヘンシェルミキサにて均一に混合したものを用い、φ90mm(粘着層用)とφ115mm(中間層用)とφ65mm(背面層用)との3台の押出機を有する口金幅2400mmのTダイ型複合製膜機を用い、上記準備した樹脂組成物をそれぞれの押出機に導入し、粘着層厚み比率22%、中間層厚み比率70%、背面層厚み比率8%となるよう各押出機の吐出量を調整し、複合Tダイから押出温度200℃にて押出し、フィルム厚み35μmの3層積層フィルムを製膜し、一旦、ロール状に巻き取った。
粘着層樹脂としては、実施例1と同一のエチレン・ヘキセン-1共重合体(直鎖状低密度ポリエチレン)を用い、中間層樹脂として、密度0.964g/cm3、融点135℃、190℃下MFR7.0g/10分の高密度ポリエチレン91重量%と粘着層構成樹脂であるエチレン・ヘキセン-1共重合体6.6重量%と後述の背面層構成樹脂組成物2.4重量%とをヘンシェルミキサにて均一に混合したものを用い、背面層樹脂として、融点163℃、230℃下MFR7.5g/10分のホモポリプロピレン98重量%と190℃下MFR2g/10分、密度0.92g/cm3の低密度ポリエチレン2重量%からなる樹脂組成物をヘンシェルミキサにて均一に混合したものを用いる以外は、実施例1と同様にTダイ型3層複合製膜機を用いて、フィルム厚み35μmの3層積層フィルムを製膜した。
各層の構成樹脂を次のように準備した。
粘着層樹脂として、リン系酸化防止剤1000ppmを含有する密度0.922g/cm3、融点116℃、190℃下MFR5.0g/10分のエチレン・ヘキセン-1共重合体(直鎖状低密度ポリエチレン)を40重量%、フェノール系酸化防止剤1200ppmを含有する密度0.875、融点71℃、190℃下MFR3.0g/10分の超低密度ポリエチレンを60重量%からなる樹脂組成物をヘンシェルミキサーにて均一混合したものを用い、中間層樹脂として、密度0.923g/cm3、190℃下MFR10g/10分の低密度ポリエチレンを、背面層樹脂として、230℃下MFR7.5g/10分、密度0.90g/cm3のホモポリプロピレン45重量%と230℃下MFR35g/10分、エチレン含有量5重量%のエチレン-プロピレンランダム共重合体45重量%と190℃下MFR2g/10分、密度0.92g/cm3の低密度ポリエチレン10重量%からなる樹脂組成物をヘンシェルミキサにて均一に混合したものを用い、φ90mm(粘着層用)とφ115mm(中間層用)とφ65mm(背面層用)との3台の押出機を有する口金幅2400mmのTダイ型複合製膜機を用い、上記準備した樹脂組成物をそれぞれの押出機に導入し、粘着層厚み比率20%、中間層厚み比率72%、背面層厚み比率8%となるよう各押出機の吐出量を調整し、複合Tダイから押出温度210℃にて押出し、フィルム厚み30μmの3層積層フィルムを製膜し、一旦、ロール状に巻き取った。背面層のポリプロピレン系の混合樹脂のMFRは、前述の計算方法で16.2g/10分である。
次いで、ロール状に巻き取ったフィルムを、スリット機に掛けて幅1300mm、長さ3,000mのサイズに仕上げ、ロール状に巻き上げたフィルムサンプルを得た。尚、スリット機にて所定幅の製品を得る際にも、離型処理等の処理を施す必要もなく、何ら抵抗なく容易にスリット機へ送り出す(巻き出す)ことができ、ブロッキングは全く認められなかった。
粘着層樹脂として、実施例1のエチレン・ヘキセン-1共重合体(直鎖状低密度ポリエチレン)100重量%に代え、密度0.93g/cm3、190℃下MFR7g/10分のMMA10重量%共重合されたエチレン・メチルメタクリレート共重合体60重量%と実施例1のエチレン・ヘキセン-1共重合体40重量%を用い、中間層樹脂として、上記粘着層に用いたものと同一のエチレン・メチルメタクリレート共重合体を用いる以外は実施例1と同様にして、フィルム厚み35μmの3層積層フィルムを製膜し、一旦、ロール状に巻き取った。
また、フィッシュアイは、実施例1と同様に視認されなかったが、フィッシュアイの被着体への転写性(被着体への凹み発生)評価を実施したところ、被着体への凹みはなく、また、背面層の凹凸による被着体への転写も認められなかった。
粘着層樹脂として190℃下MFR7g/10分のMMA10重量%共重合されたエチレン・メチルメタクリレート共重合体100重量%を用いる以外は実施例1と同様にして、
フィルム厚み35μm、幅1600mm、長さ7,000mの3層積層フィルムを仕上げた。尚、所定幅の製品を得る際にも、何ら抵抗なく容易にスリット機へ送り出す(巻き出す)ことができ、ブロッキングは全く認められなかった。
各層の構成樹脂を次ぎのように準備した。
粘着層樹脂としては、比較例1と同一のエチレン・ヘキセン-1共重合体(直鎖状低密度ポリエチレン)を用い、中間層樹脂として、密度0.964g/cm3、融点134℃、190℃下MFR7.5g/10分の高密度ポリエチレンを、背面層樹脂として、190℃下MFR5.5g/10分、密度0.923g/cm3の低密度ポリエチレン94重量%、190℃下MFR2g/10分、密度0.92g/cm3の低密度ポリエチレン1重量%、230℃下MFR40g/10分、エチレン含有量5重量%のエチレン-プロピレンランダム共重合体4重量%に加え、滑剤として平均粒子径2.0μmのソジウムカルシウムアルミノシリケート1.0重量%からなる樹脂組成物をヘンシェルミキサにて均一に混合したものを用い、実施例2と同様にTダイ型3層複合製膜機を用いて、フィルム厚み30μmの3層積層フィルムを製膜した。
中間層樹脂として、実施例2の粘着層に用いたものと同一の密度0.875g/cm3、MFR3g/10分の超低密度ポリエチレンを用いる以外は実施例1と同様にして実施例5のフィルムを得た。
Claims (3)
- 粘着層と中間層と背面層の3層積層形態からなり、該粘着層は、エチレン・α-オレフィン共重合体およびエチレン・メチルメタクリレート共重合体からなる群より選ばれた少なくとも1種からなり、該中間層は密度0.870~0.935g/cm3のポリエチレン系樹脂およびエチレン・メチルメタクリレート共重合体からなる群より選ばれた少なくとも1種を含有し、該背面層は、ポリプロピレン系樹脂と低密度ポリエチレンから構成されてなり、該背面層の表面粗さが算術平均粗さ(Ra)として0.6μm以上、十点平均粗さ(Rz)で4μm以上であることを特徴とする表面保護フィルム。
- 背面層を構成するポリプロピレン系樹脂の230℃、荷重2.16kg/cm2下でのメルトフローレートが5~50g/10分の範囲であって、かつ、低密度ポリエチレンの190℃、荷重2.16kg/cm2下でのメルトフローレートが0.5~5g/10分であることを特徴とする請求項1記載の表面保護フィルム。
- 粘着層と中間層と背面層の3層積層形態からなり、中間層が、密度0.870~0.935g/cm3のポリエチレン系樹脂およびエチレン・メチルメタクリレート共重合体からなる群より選ばれた少なくとも1種と、粘着層構成樹脂及び背面層構成樹脂との混合樹脂組成からなることを特徴とする請求項1または2に記載の表面保護フィルム。
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EP11768688.1A EP2559745A4 (en) | 2010-04-13 | 2011-03-10 | SURFACE PROTECTION FILM |
KR1020127028161A KR101808140B1 (ko) | 2010-04-13 | 2011-03-10 | 표면 보호 필름 |
CN201180019027.XA CN102844393B (zh) | 2010-04-13 | 2011-03-10 | 表面保护膜 |
JP2011515618A JP5761571B2 (ja) | 2010-04-13 | 2011-03-10 | 表面保護フィルム |
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JP2013124306A (ja) * | 2011-12-15 | 2013-06-24 | Okura Ind Co Ltd | 表面保護フィルム |
JP2015004003A (ja) * | 2013-06-21 | 2015-01-08 | 日東電工株式会社 | 粘着シート |
JP2015044979A (ja) * | 2013-07-31 | 2015-03-12 | 日本ポリプロ株式会社 | 医療用プロピレン−エチレン系樹脂組成物及びその射出成形品 |
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JP2018119138A (ja) * | 2017-01-20 | 2018-08-02 | 東レ株式会社 | 積層フィルム |
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CN102844393B (zh) | 2014-06-18 |
EP2559745A4 (en) | 2014-01-01 |
KR101808140B1 (ko) | 2017-12-13 |
KR20130056230A (ko) | 2013-05-29 |
JP5761571B2 (ja) | 2015-08-12 |
US20130052418A1 (en) | 2013-02-28 |
JPWO2011129167A1 (ja) | 2013-07-11 |
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