JP2014131871A - Laminate film and production method of the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a laminate film having high hardness, superior suppressing property for oligomer precipitation, and releasability.SOLUTION: The laminate film includes a resin layer (X) formed by using a resin (α) on at least one surface of a polyester film, and satisfies the following conditions (1) to (5). (1) The resin layer (X) has a thickness of 80 nm or more. (2) The resin (α) has a glass transition temperature of 50°C or higher. (3) The resin layer (X) has a surface free energy of 40 mN/m or more and less than 50 mN/m. (4) The resin (α) is obtained from a resin composition comprising a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group. (5) The laminated film has a haze of greater than 3.0%.

Description

  The present invention relates to a laminated film in which a resin layer is laminated on a thermoplastic resin film, particularly a polyester film. More specifically, a resin layer that suppresses scratches on the film surface that occurs in the process of film formation and conveyance of the polyester film, suppresses oligomers that precipitate from the polyester film in a processing process that involves heat treatment, and is excellent in releasability. It is related with the laminated film which has.

  Thermoplastic resin films, especially biaxially stretched polyester films, have excellent properties such as mechanical properties, electrical properties, dimensional stability, transparency, and chemical resistance. Widely used as a substrate film in applications. Particularly in recent years, there has been an increasing demand for various optical films including antireflection materials and polarizing plate materials for flat panel displays, or protective films and release films used in these processes. In these applications, coating processing that imparts various functions and heat treatment processing are often performed.

  However, for example, scratches may occur on the film surface due to rubbing with the transport roll in the transport process during the production of the polyester film, or oligomer precipitation from the polyester film may occur due to heat treatment in the processing process, resulting in whitening or contamination of the film surface. In some cases, it is not practically applicable as a release film.

  Therefore, a release film in which a release layer made of alkyd resin, acrylic resin, melamine resin and silicone is laminated on a plastic film (Patent Document 1), and a release film in which a release layer made of melamine resin is laminated (patent) Reference 2) has been studied. Moreover, the method of providing a coating film using a thermosetting acrylic resin and a crosslinking agent by an in-line coating method in which coating is performed in the process of manufacturing a thermoplastic resin film (Patent Document 3), and further adding a thermal initiator to the coating film A method (Patent Document 4) for improving the hardness has been proposed.

JP 2004-82370 A JP 2006-7568 A JP 2005-89622 A Special table 2008-524402

  However, the method of providing a resin layer made of alkyd resin, acrylic resin, melamine resin and silicone on the surface of a plastic film as in Patent Document 1 has the following drawbacks. In order to increase the hardness of the resin layer and create a laminated film having the ability to suppress oligomer precipitation from the polyester film (oligomer precipitation suppression), the resin layer needs to have a thickness of several μm. Moreover, since silicone is used, there is a possibility that the silicone may be transferred to the film forming process or product and contaminated. Furthermore, since the surface free energy of the resin layer becomes too low, there is a drawback that, for example, repelling occurs when an aqueous solvent coating layer is laminated. Moreover, in the method of providing a resin layer using the thermosetting melamine resin, acrylic resin, and crosslinking agent like patent document 2, 3, the hardness of a resin layer and oligomer precipitation inhibitory property are not enough. Especially when used as a release film, when the product is laminated on the release film and peeled off through a heating process, foreign substances derived from oligomers are included in the product or adhere to the surface. There is a problem that becomes a drawback. The resin layer described in Patent Document 4 requires a resin layer thickness of several μm as in Patent Document 1, and further requires a thermal initiator to form a coating layer, and is an organic solvent or a solvent-free type. Use is limited to the coating layer.

  Accordingly, an object of the present invention is to provide a laminated film having a resin layer (X) that eliminates the above-mentioned drawbacks and has high hardness and excellent oligomer precipitation inhibition and release properties.

The present invention has the following configuration. That is,
A laminated film in which a resin layer (X) using a resin (α) is provided on at least one surface of a polyester film, which satisfies the following conditions (1) to (5).
(1) The thickness of the resin layer (X) is 80 nm or more. (2) The resin (α) is a resin having a glass transition temperature of 50 ° C. or more. (3) Surface free energy of the resin layer (X) (4) The resin (α) is obtained from a resin composition containing a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group. (5) The haze of the laminated film is greater than 3.0%.

  The laminated film of the present invention not only has excellent releasability, but also prevents the occurrence of scratches in the transport process and processing process, and precipitates oligomers from the polyester film, which is a base film that becomes a problem during heat treatment. There is an inhibitory effect.

  Hereinafter, the laminated film of the present invention will be described in detail.

  The present invention is a laminated film in which a resin layer (X) is laminated on at least one surface of a polyester film as a base film.

(1) Resin layer (X)
The resin layer (X) of the laminated film of the present invention requires that the resin layer (X) has a thickness of 80 nm or more. By setting the thickness of the resin layer (X) to 80 nm or more, it becomes possible to impart oligomer precipitation inhibitory properties and releasability to the resin layer (X). The upper limit of the thickness of the resin layer (X) is not particularly limited, but is preferably 500 nm or less from the viewpoint of the handling properties of the laminated film. The resin (α) forming the resin layer (X) of the laminated film of the present invention needs to be a resin having a glass transition temperature of 50 ° C. or higher. By making the resin (α) a resin having a glass transition temperature of 50 ° C. or higher, the hardness of the resin layer (X) is increased, and therefore, oligomer precipitation suppression and scratch suppression are imparted to the resin layer (X). In addition, the resin layer (X) can exhibit good releasability because permeation and erosion of organic solvents and resins are suppressed.

  Resin (α) forming resin layer (X) of the laminated film of the present invention is a resin obtained from a resin composition comprising a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group If it is, the resin (α) can be a resin having a glass transition temperature of 50 ° C. or higher. Moreover, it is preferable that the glass transition temperature of resin (A) which has a hydroxyl group and an acryloyl group is 50 degreeC or more. When the glass transition temperature of the resin (A) is 50 ° C. or higher, the glass transition temperature of the resin (α) can be made higher.

  Furthermore, the resin layer (X) of the laminated film of the present invention needs to have a surface free energy of 40 mN / m or more and less than 50 mN / m. By setting the surface free energy of the resin layer (X) to 40 mN / m or more, the repelling of the coating layer applied on the resin layer (X) can be suppressed when used as a release film. On the other hand, when the surface free energy of the resin layer (X) is less than 50 mN / m, when used as a release film, good release properties can be imparted to the resin layer (X).

  The laminated film of the present invention needs to have a haze greater than 3.0%. By setting the haze of the laminated film to be greater than 3.0%, a laminated film having excellent scratch inhibiting properties and releasability can be obtained. For example, pigments, dyes, organic or inorganic particles are included in the polyester film or the resin layer (X) as the base film, and the haze is made larger than 3.0%, so that minute projections are formed on the surface of the laminated film. Is formed, and it becomes possible to give scratch resistance and releasability to the laminated film. On the other hand, if the haze of the laminated film is 3.0% or less, the film is inferior in scratch resistance and releasability. The haze of the laminated film is preferably 5.0% or more, and more preferably 8.0% or more.

Resin ((alpha)) which forms resin layer (X) of the laminated | multilayer film of this invention is resin obtained from the resin composition containing the resin (A) which has a hydroxyl group and an acryloyl group, and the melamine compound (B) which has a methylol group Need to be. When the resin (α) is a resin obtained from a resin composition containing a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group, the resin layer (X) has a good mold release Property, scratch generation inhibiting property and oligomer precipitation inhibiting property can be imparted. When the resin (α) forming the resin layer (X) is a resin obtained from a resin composition containing a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group, The surface free energy of the resin layer (X) can be easily set to 40 mN / m or more and less than 50 mN / m. The resin (A) has a hydroxyl group that is a hydrophilic group, the melamine compound (B) has a methylol group that is a hydrophilic group, and the resin (A) is a hydrophobic functional group. Since it has a certain acryloyl group, the surface free energy of the resin layer (X) can be adjusted by setting the number and weight ratio of the functional groups of the resin (A) and the melamine compound (B). . Furthermore, the resin (A) is preferably an acrylic resin that is polymerized using at least the following compounds (a) to (c).
By using the compounds (a) to (c), the surface free energy of the melamine compound (B) and the obtained resin layer (X) can be adjusted to a range of 40 mN / m or more and less than 50 mN / m.
Acrylic acid ester compound and / or methacrylic acid ester compound (a)
-An ethylenically unsaturated compound having a hydroxyl group (b)
Compound (c) having a chemical structure (urethane structure) represented by formula (3) and a polyfunctional acryloyl group
In the laminated film of the present invention, the resin layer (X) preferably has a pencil hardness of “F” or higher. By setting the pencil hardness of the resin layer (X) to “F” or more, it is possible to suppress the occurrence of scratches in the film-forming process and the conveying process during processing.

  The laminated film of the present invention is a laminated film in which a resin layer (X) made of resin (α) is provided on at least one surface of a polyester film. Details of the resin (α) will be described later.

  Moreover, the resin layer (X) of the laminated film of the present invention has a total mass of the resin (α), the resin (A) having a hydroxyl group and an acryloyl group, and the melamine compound (B) having a methylol group. X) It is preferable that it is 70 mass% or more of the whole. By making the total content of the resin (α), the resin (A), and the melamine compound (B) in the resin layer (X) 70% by mass or more, it is possible to prevent scratches and suppress oligomer precipitation. .

  The resin (α) is a resin obtained from a resin composition comprising a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group. When the resin composition comprising the resin (A) and the melamine compound (B) is heated, the acryloyl groups of the resin (A) are cross-linked to form a cross-linked structure, or the hydroxyl group of the resin (A) and the melamine compound The methylol group of (B) is crosslinked to form a crosslinked structure (structure represented by the formula (1) described later), or the methylol groups of the melamine compound (B) are crosslinked to each other to form a crosslinked structure (formula (described below) 2) is formed. Since the cross-linking reaction between the acryloyl groups of the resin (A), the hydroxyl groups of the resin (A) and the methylol groups of the melamine compound (B), and the methylol groups of the melamine compound (B) is highly reactive, the resin (α) is It becomes a resin having many cross-linked structures. Increasing the number of hydroxyl groups and acryloyl groups in the resin (A) and the number of methylol groups in the melamine compound (B) makes it possible to obtain a resin (α) with a more dense cross-linked structure.

  That is, in the present invention, the resin forming the resin layer (X) preferably has a crosslinked structure of acryloyl groups. Moreover, it is preferable that resin which forms resin layer (X) has the crosslinked structure (chemical structure) of the hydroxyl group and methylol group which are shown by Formula (1). Moreover, it is preferable that resin which forms resin layer (X) has the crosslinked structure of methylol groups shown by Formula (2). In addition, in order to obtain a resin (α) having a denser cross-linked structure, the resin (α) is obtained by adding a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group at 150 ° C. It is preferable that it is a resin composition obtained by heating above.

  Thus, since the resin layer (X) and the resin (α) have a dense cross-linked structure, the hardness of the resin layer (X) can be dramatically increased. In addition, it is difficult to be scratched in the transport process and the processing process, and a laminated film with less oligomer precipitation after heating can be obtained. In particular, even when the laminated film of the present invention is subjected to heat treatment at 150 ° C. for 1 hour, the change rate of haze, which is an index of the amount of oligomer precipitation, remains at 0.3% or less. Therefore, the laminated film of the present invention is suitably used as a release film. Since the resin layer (X) and the resin (α) have a dense cross-linked structure, penetration and erosion of organic solvents and resins are suppressed, and not only good release properties can be exhibited, but also oligomer precipitation suppression and scratch resistance. Therefore, the quality of the product peeled from the release film, particularly the number of defects, can be greatly reduced, and the surface smoothness can be made extremely good.

  The resin layer (X) of the laminated film of the present invention is formed by using the resin (α), and the production method is not particularly limited as long as it satisfies the above-described conditions, but a resin having a hydroxyl group and an acryloyl group ( It can be produced by applying a resin composition comprising A) and a melamine compound (B) having a methylol group to a polyester film (base film) and heating to 150 ° C. or more.

(2) Resin (α) and Crosslinked Structure As described above, the resin (α) used in the present invention is a resin composition comprising a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group. It is a resin obtained from a product. In particular, when the resin (α) is obtained by heating the resin (A) having a hydroxyl group and an acryloyl group and the melamine compound (B) having a methylol group to 150 ° C. or higher, a dense cross-linked structure is formed. preferable. The resin (α) and the like will be described in detail below.

  In order to improve the hardness of the resin layer (X), oligomer precipitation suppression, release properties, and the like, the resin layer (X) and the resin (α) preferably have the following structure.

  First, the resin (α) preferably has a structure obtained by crosslinking between acryloyl groups. That is, the resin forming the resin layer (X) preferably has a structure obtained by crosslinking between acryloyl groups. Such a crosslinked structure can be formed by heating the resin (A) having an acryloyl group.

  Next, the resin (α) preferably has a structure represented by the formula (1).

  The structure shown in Formula (1) is a structure obtained by crosslinking of a hydroxyl group and a methylol group. That is, it is preferable that the resin forming the resin layer (X) has a chemical structure represented by the formula (1) obtained by crosslinking of a hydroxyl group and a methylol group. Such a crosslinked structure can be formed by heating the resin (A) having a hydroxyl group and the melamine compound (B) having a methylol group. Since the resin or resin (α) forming the resin layer (X) has the structure represented by the formula (1), the resin layer (X) can have high hardness, oligomer precipitation inhibiting property, and releasability. .

  Furthermore, the resin (α) preferably has a structure represented by the formula (2).

  The structure shown in Formula (2) is a structure obtained by cross-linking of methylol groups. That is, it is preferable that the resin forming the resin layer (X) has a chemical structure represented by the formula (2) obtained by crosslinking between methylol groups. Such a crosslinked structure can be formed by heating the melamine compound (B) having a methylol group. The resin or resin (α) forming the resin layer (X) has the structure shown in the formula (2), so that the resin layer (X) can have high hardness, oligomer precipitation inhibiting property, and releasability. .

  In addition, the resin (α) preferably has a structure represented by the formula (3).

  The structure shown in Formula (3) is a urethane structure. That is, the resin forming the resin layer (X) preferably has a chemical structure of the formula (3). Such a structure can be introduced into the resin (α) by using, for example, a resin (A) having a urethane structure in addition to a hydroxyl group and an acryloyl group. The resin or resin (α) forming the resin layer (X) has the structure shown in the formula (3), so that the resin layer (X) can have elasticity and elasticity. That is, when the resin (α) is formed (when a crosslinked structure of acryloyl groups or a crosslinked structure represented by the formulas (1) and (2) is formed), a crack occurs in the resin layer (X). The resin and resin (α) forming the resin layer (X) may have the structure of the formula (3) to suppress the generation of cracks and curls. it can.

In the present invention, when the resin (α) is obtained using the resin (A) and the melamine compound (B), the resin composition (resin (A) and melamine compound (B) for forming the resin layer (X) is used. In the mixture), the mass ratio of the resin (A) to the melamine compound (B) is 30 parts by mass or more and 100 parts by mass or less when the mass of the resin (A) is 100 parts by mass. It is preferable that More preferably, the mass of the melamine compound (B) is 30 parts by mass or more and 60 parts by mass or less. By setting the mass of the melamine compound (B) to 30 parts by mass or more, the resin (α) can be sufficiently provided with the structure of the formula (2). As a result, it is possible not only to increase the hardness of the resin layer (X) but also to significantly suppress oligomer precipitation. In addition, the releasability of the resin layer (X) is enhanced, and further, flexibility, toughness, and solvent resistance are enhanced. On the other hand, the hardening shrinkage | contraction which generate | occur | produces when the structure of Formula (2) is formed can be suppressed because the mass of a melamine compound (B) shall be 100 mass parts or less. As a result, the occurrence of cracks in the resin layer (X) is suppressed, and oligomer precipitation suppression and releasability can be exhibited.
(3) Resin (A) having hydroxyl group and acryloyl group
The resin (A) having a hydroxyl group and an acryloyl group used in the present invention is a resin having at least one hydroxyl group and one or more acryloyl groups. In the present invention, the acryloyl group includes a methacryloyl group. The acryloyl group is preferably polyfunctional from the viewpoint that the resin layer (X) forms a dense cross-linked structure, and the number of acryloyl groups is preferably 2 or more and 15 or less.

  In the present invention, the resin (A) has a hydroxyl group and an acryloyl group as long as the resin (A) can be formed together with the melamine compound (B) by heating the resin (A) in any form. You may do it. For example, a resin having a polymer having a hydroxyl group and a polymer having an acryloyl group may be used, or a resin having a polymer having a hydroxyl group and an acryloyl group as a repeating unit may be used. Among them, an acrylic ester compound and / or a methacrylic ester compound (a), an ethylenically unsaturated compound (b) having a hydroxyl group, a chemical structure (urethane structure) represented by formula (3) and a polyfunctional acryloyl group A resin having a polymer obtained by polymerizing these compounds using compound (c) is preferable. In terms of forming a dense cross-linked structure, it is more preferable to have a polymer in which (b) and (c) are randomly graft-polymerized on the hydrocarbon chain formed from (a). Resin (A) polymerized using these monomers ((a), (b) and (c)) can form the above-mentioned resin (α) by heating together with the melamine compound (B). it can. In particular, heating to 150 ° C. or higher is preferable because a resin (α) having a dense cross-linked structure can be obtained. Hereinafter, the compounds (a), (b) and (c) will be described.

Acrylic ester compound and / or methacrylic ester compound (a):
The compound (a) is a monomer that forms the main skeleton of the resin (A). Specific examples of the compound (a) include methyl acrylate, ethyl acrylate, n-propyl acrylate, i-propyl acrylate, n-butyl acrylate, i-butyl acrylate, t-butyl acrylate, and acrylic acid. n-octyl, i-octyl acrylate, t-octyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, i-propyl methacrylate, n-butyl methacrylate, methacrylic acid C 1-18 alkyl of acrylic acid and / or methacrylic acid such as i-butyl, t-butyl methacrylate, n-octyl methacrylate, i-octyl methacrylate, t-octyl methacrylate, 2-ethylhexyl methacrylate Esters and other esters such as cyclohexyl acrylate Cycloalkyl esters of (b) 5 to 12 carbon atoms, and the like aralkyl ester of acrylic acid benzyl having 7 to 12 carbon atoms.

  When the resin (A) is polymerized using the compounds (a), (b) and (c), the mass of the compound (a) is 100 parts by mass of the total mass of the compounds (a) to (c). Is preferably 55 parts by mass or more and 98 parts by mass or less. The resin (A) can be efficiently polymerized by setting the mass (preparation amount) of the compound (a) within the above numerical range.

Ethylenically unsaturated compound (b) having a hydroxyl group:
The compound (b) needs to have a hydroxyl group. By using the compound (b) as a monomer, the resin (A) can have a hydroxyl group.

  Specific examples of the compound (b) include 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 3-hydroxypropyl acrylate, 2-hydroxybutyl acrylate, 3-hydroxybutyl acrylate, and 4-hydroxy acrylate. Butyl, 6-hydroxyhexyl acrylate, 2-hydroxyethyl allyl ether, 2-hydroxypropyl allyl ether, 2-hydroxybutyl allyl ether, allyl alcohol, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, methacrylic acid 3 -Hydroxypropyl, 2-hydroxybutyl methacrylate, 3-hydroxybutyl methacrylate, 4-hydroxybutyl methacrylate, 6-hydroxyhexyl methacrylate, 2-hydroxyethyl methacrylate Le, 2-hydroxypropyl methallyl ether, unsaturated compounds containing one or more hydroxyl groups in the molecule such as 2-hydroxybutyl methallyl ether.

  Moreover, the compound (b) may have a carboxyl group.

  When polymerizing the resin (A) using the compounds (a), (b) and (c), the mass of the compound (b) is 100 parts by mass of the total mass of the compounds (a) to (c). Is preferably 1 part by mass or more and 30 parts by mass or less. By setting the mass (preparation amount) of the compound (b) to 1 part by mass or more, the resin (A) can have a sufficient amount of hydroxyl groups. Moreover, resin (A) can be efficiently polymerized because the mass of a compound (b) shall be 30 mass parts or less. When the mass of the compound (b) exceeds 30 parts by weight, the resin (A) dispersed in water or water-solubilized in the aqueous solvent (E) becomes a gel when preparing a coating liquid containing a resin composition by the method described later. Or agglomerate, making it difficult to use suitably.

Compound (c) having chemical structure (urethane structure) represented by formula (3) and polyfunctional acryloyl group:
The compound (c) used in the present invention needs to have a polyfunctional acryloyl group. In the present invention, the acryloyl group includes a methacryloyl group. By using the compound (c) as a monomer, the resin (A) can have an acryloyl group. In addition to the polyfunctional acryloyl group, the compound (c) preferably has a urethane structure in the molecule. By using such a compound (c) as a monomer, the resin (A) can have an acryloyl group and a urethane structure.

  Specifically, the compound (c) includes a compound obtained by reacting a polyhydric alcohol, an isocyanate monomer and / or an organic polyisocyanate, an acrylate monomer having a hydroxyl group and / or a methacrylate monomer having a hydroxyl group, A urethane acrylate compound obtained by reacting and synthesizing in a solvent-free or organic solvent is preferred.

  Examples of the polyhydric alcohol include acrylic polyols, polyester polyols, polycarbonate polyols, ethylene glycol, and propylene glycol. Isocyanate monomers include tolylene diisocyanate, diphenylmethane diisocyanate, xylylene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, and organic polyisocyanates include adduct type, isocyanurate type and burette type polyisocyanates synthesized from isocyanate monomers. Can be mentioned. Examples of the acrylate monomer having a hydroxyl group include 2-hydroxyethyl acrylate, 2-hydroxy-3-phenoxypropyl acrylate, isocyanuric acid ethylene oxide-modified diacrylate, pentaerythritol tri- and tetraacrylate, and dipentaerythritol pentaacrylate. Examples of the methacrylate monomer having a hydroxyl group include 2-hydroxyethyl methacrylate and hydroxypropyl methacrylate. The compound (c) may contain a methylol group.

  When the resin (A) is polymerized using the compounds (a), (b) and (c), the mass of the compound (c) is 100 parts by mass of the total mass of the compounds (a) to (c). It is preferable that it is 1 to 15 mass parts. By setting the mass of the compound (c) to 1 part by mass or more, the resin (A) can have a sufficient amount of acryloyl group or urethane structure.

  On the other hand, when the mass of the compound (c) exceeds 15 parts by mass, the following phenomenon may occur, which is not preferable. That is, since the resin (A) has an excessive amount of acryloyl groups, if this is heated to obtain the resin (α), a very large number of crosslinked structures of acryloyl groups are formed. As a result, significant curing shrinkage is caused, and cracks may occur in the resin layer (X). Moreover, even if the resin (A) is heated to obtain the resin (α), the hardness of the resin (α) cannot be sufficiently increased, and the hardness of the resin layer (X) may be inferior.

(4) Production Method of Resin (A) Having Hydroxyl Group and Acrylyl Group The production method of the resin (A) used in the present invention is not particularly limited, and a known technique can be applied. It is preferable to use the compounds (a), (b) and (c). Furthermore, as a manufacturing method of resin (A), it is preferable to manufacture by emulsion polymerization in an aqueous solvent (E) using compounds (a), (b) and (c). By using the aqueous solvent (E), it becomes easy to adjust the coating liquid containing the resin composition using the aqueous solvent (E). Further, it is preferable to produce the resin (A) by emulsion polymerization because the mechanical dispersion stability of the resin (A) is excellent.

  The emulsifier used in the present invention is not particularly limited by any of an anionic emulsifier and a nonionic emulsifier, and may be used alone or in combination of two or more.

  Examples of the anionic emulsifier include higher fatty acid salts such as sodium oleate, alkylaryl sulfonates such as sodium dodecylbenzenesulfonate, and alkyl sulfate esters such as sodium lauryl sulfate. Examples of nonionic emulsifiers include polyoxyethylene alkyl ethers such as polyoxyethylene lauryl ether and polyoxyethylene octylphenyl ethers.

  In the emulsion polymerization, for example, persulfates such as sodium persulfate, potassium persulfate and ammonium persulfate, and organic peroxides such as t-butyl hydroperoxide, cumene hydroperoxide and p-menthane hydroperoxide are usually used. A polymerization initiator such as hydrogen peroxide is used. These polymerization initiators can also be used in any form of one kind or a combination of plural kinds.

  In emulsion polymerization, a reducing agent can be used in combination with a polymerization initiator as desired. Examples of such reducing agents include reducing organic compounds such as ascorbic acid, tartaric acid, citric acid, glucose, and formaldehyde sulfoxylate metal salts; sodium thiosulfate, sodium sulfite, sodium bisulfite, sodium metabisulfite, A reducing inorganic compound such as ammonium sulfite can be used.

  Furthermore, a chain transfer agent can be used in the emulsion polymerization. Examples of such chain transfer agents include n-dodecyl mercaptan, t-dodecyl mercaptan, n-butyl mercaptan, 2-ethylhexyl thioglycolate, 2-mercaptoethanol, trichlorobromomethane and the like. The polymerization temperature suitably employed in the emulsion polymerization of the resin (A) of the present invention is about 30 to 100 ° C.

(5) Melamine compound having a methylol group (B)
The melamine compound (B) that can be used in the present invention needs to have at least one triazine ring and one methylol group in one molecule. By using such a melamine compound (B), the resin (α) can have a cross-linked structure between methylol groups represented by the formula (2).

  Specifically, the melamine compound (B) is a compound obtained by dehydrating and condensing methyl alcohol melamine derivative obtained by condensing melamine and formaldehyde with methyl alcohol, ethyl alcohol, isopropyl alcohol or the like as a lower alcohol. Is preferred.

  Examples of methylolated melamine derivatives include monomethylol melamine, dimethylol melamine, trimethylol melamine, tetramethylol melamine, pentamethylol melamine, and hexamethylol melamine.

(6) Compound (C) having one or more functional groups selected from the group consisting of methylol group, amino group, isocyanate group, epoxy group, alkoxysilane group, oxazoline group, carboxyl group and carbodiimide group:
In the present invention, in addition to the resin (α), the resin (A), and the melamine compound (B), the resin layer (X) is a methylol group, amino group, isocyanate group, epoxy group, alkoxysilane group, oxazoline group, carboxyl group. And a compound (C) having one or more functional groups selected from the group consisting of carbodiimide groups. The mass of the compound (C) is preferably 30% by mass or less when the entire resin layer (X) is 100% by mass. While the mass of the compound (C) is 30% by mass or less, it is possible to maintain the excellent properties such as the resin layer (X) hardness, the oligomer precipitation inhibiting property, and the release property, which are the effects of the resin (α). Properties such as flexibility and toughness can be improved.

  As the compound having a methylol group, N-methylol acrylamide, N-methylol methacrylamide or the like, which is an unsaturated carboxylic acid amide having a methylol group, is preferably used alone or in combination of two or more.

  Compounds having an amino group include aminoethyl acrylate, dimethylaminoethyl acrylate, diethylaminoethyl acrylate, butylaminoethyl acrylate, aminoethyl methacrylate, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, butylamino methacrylate Examples include aminoalkyl esters such as ethyl, and carboxylic acid aminoalkylamides such as aminoethylacrylamide, dimethylaminomethylacrylamide, methylaminopropylacrylamide, aminoethylmethacrylamide, dimethylaminomethylmethacrylamide, and methylaminopropylmethacrylamide. .

  As compounds having an isocyanate group, 1,3- or 1,4-phenylene diisocyanate, 2,4- or 2,6-tolylene diisocyanate, 1,5-naphthylene diisocyanate, 4,4-diphenylmethane diisocyanate Aromatic polyisocyanate compounds such as 3,3-dimethyldiphenylmethane-4,4-diisocyanate, 1,3-xylylene diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 2,2 , 4-trimethyl-1,6-hexamethylene diisocyanate, 1,8-octamethylene diisocyanate, 1,10-decamethylene diisocyanate and the like, or dimers or trimers of these isocyanates and their isocyanates When, for example, ethylene glycol, adduct of divalent or trivalent polyols such as trimethylolpropane and the like can be exemplified.

  Examples of the compound having an epoxy group include glycidyl acrylate, acrylate 3,4-epoxycyclohexylmethyl, glycidyl allyl ether, glycidyl vinyl ether, 3,4-epoxycyclohexyl vinyl ether, glycidyl methacrylate, methacrylic acid 3,4-epoxycyclohexylmethyl. And glycidyl methallyl ether.

  Examples of the compound having alkoxysilane include vinyltrimethoxysilane, vinyltriethoxysilane, vinyltri (βmethoxyethoxy) silane, β- (3,4epoxycyclohexyl) ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropyltriethoxysilane, γ- Methacryloxypropylmethyldiethoxysilane, N-β (aminoethyl) γ-aminopropyltrimethoxysilane, N-β (aminoethyl) γ-aminopropylmethyldimethoxysilane, N-β (aminoethyl) γ-aminopropyltri Ethoxysilane, Examples thereof include γ-aminopropyltrimethoxysilane and γ-aminopropyltriethoxysilane.

  The compound having an oxazoline group is not particularly limited as long as it has at least one oxazoline group or oxazine group per molecule, but an addition polymerizable oxazoline group-containing monomer is preferable, and 2-vinyl-2-oxazoline, 2 -Vinyl-4-methyl-2-oxazoline, 2-vinyl-5-methyl-2-oxazoline, 2-isopropenyl-2-oxazoline, 2-isopropenyl-4-methyl-2-oxazoline, 2-isopropenyl- Mention may be made of 5-ethyl-2-oxazoline.

  The compound having a carboxyl group is not particularly limited as long as it is an unsaturated compound containing one or more carboxyl groups in the molecule, but acrylic acid, methacrylic acid, maleic acid, maleic anhydride, fumaric acid, crotonic acid, Itaconic acid and the like can be mentioned.

The compound having a carbodiimide group is not particularly limited as long as it has at least one carbodiimide structure represented by the following formula (4) per molecule. Particularly preferred are polycarbodiimide compounds having two or more in them. In particular, when a polymer type isocyanate compound having a plurality of carbodiimide groups is used at the terminal or side chain of a polymer such as polyester resin or acrylic resin, the resin layer (X) of the present invention is provided on the polyester film, When a laminated film is used, not only the hardness of the resin layer (X) is improved and the oligomer precipitation is suppressed, but also flexibility and toughness are increased, so that it can be preferably used.
-N = C = N- (4)
A known technique can be applied to the production of the carbodiimide compound, and it is generally obtained by polycondensation of a diisocyanate compound in the presence of a catalyst. As the diisocyanate compound that is a starting material of the polycarbodiimide compound, aromatic, aliphatic, and alicyclic diisocyanates can be used. Specifically, tolylene diisocyanate, xylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, cyclohexane diisocyanate. , Isophorone diisocyanate, dicyclohexyl diisocyanate and the like can be used. Furthermore, in order to improve the water solubility and water dispersibility of the polycarbodiimide compound within the range not losing the effect of the present invention, a surfactant is added, polyalkylene oxide, quaternary ammonium salt of dialkylamino alcohol, hydroxy A hydrophilic monomer such as an alkyl sulfonate may be added or used.

  Other compounds such as aziridine compounds, amide epoxy compounds, titanate coupling agents such as titanium chelates, methylolated or alkylolated urea compounds, acrylamide compounds, and the like can be optionally used.

(7) Release agent In this invention, it is preferable to contain a release agent other than resin (A) and a melamine compound (B) in the resin composition which forms resin layer (X). As for a mold release agent, when the mass of resin (A) is 100 mass parts, it is preferable that the mass of a mold release agent is 5 mass parts or more and 30 mass parts or less. More preferably, it is 10 mass parts or more and 25 mass parts or less. The release property of the resin layer (X) can be improved by making the mass of the release agent 5 parts or more, and the hardness of the resin layer (X) can be increased by being 30 parts by mass or less. Further, it is possible to maintain an excellent property of suppressing oligomer precipitation.

  The release agent as used in the present invention refers to a compound having a release property (that is, lowering the surface energy of the resin or lowering the static friction coefficient of the resin) on the surface of the resin when added to the resin. .

  Examples of the release agent (release agent (D)) that can be used in the present invention include silicone-containing compounds, waxes such as paraffin wax, polyethylene wax, and carnauba wax, long-chain alkyl group-containing compounds, and resins. . Among these, a long-chain alkyl chain-containing acrylic resin is preferable in terms of achieving both mold release and oligomer suppression.

  The long-chain alkyl group-containing acrylic resin preferably has a long-chain alkyl group having 12 or more carbon atoms. Specifically, an acrylic resin synthesized from an acrylic monomer having an alkyl group having 12 or more carbon atoms in the side chain, an acrylic monomer having an alkyl group having 12 or more carbon atoms in the side chain, and the acrylic monomer can be copolymerized. A copolymer acrylic resin with an acrylic monomer is mentioned. By setting the number of carbon atoms to 12 or more, a release effect sufficient as the release agent (D) can be exhibited. The upper limit of the carbon number of the long-chain alkyl group is not particularly limited, but is preferably 25 or less because production is easy.

(8) Polyester film In the laminated film of this invention, the polyester film used as a base film is demonstrated in detail. Polyester is a general term for polymers having an ester bond as a main bond chain, and includes ethylene terephthalate, propylene terephthalate, ethylene-2,6-naphthalate, butylene terephthalate, propylene-2,6-naphthalate, ethylene. Those having at least one component selected from -α, β-bis (2-chlorophenoxy) ethane-4,4'-dicarboxylate as a main component can be preferably used. In the present invention, it is preferable to use polyethylene terephthalate as the polyester film. When heat or shrinkage stress acts on the thermoplastic resin film, polyethylene-2,6-naphthalate having excellent heat resistance and rigidity is particularly preferable.

  The polyester film is preferably biaxially oriented. A biaxially oriented polyester film is generally an unstretched polyester sheet or film that is stretched about 2.5 to 5 times in the longitudinal direction and in the width direction perpendicular to the longitudinal direction, and then subjected to heat treatment to produce crystals. The alignment is completed, and it indicates a biaxial alignment pattern by wide-angle X-ray diffraction. When the polyester film is not biaxially oriented, the thermal stability of the laminated film, particularly the dimensional stability and mechanical strength are insufficient, or the flatness is poor.

  In addition, various additives such as antioxidants, heat stabilizers, weather stabilizers, UV absorbers, organic lubricants, pigments, dyes, organic or inorganic particles, fillers, antistatic agents are included in the polyester film. An agent, a nucleating agent, etc. may be added to such an extent that the properties are not deteriorated. In particular, when pigments, dyes, organic or inorganic particles are added, the haze of the laminated film can be made larger than 3.0% to roughen the surface of the laminated film. Can be suitably used. When the content of pigments, dyes, organic or inorganic particles contained in the polyester film is 1.0 to 10.0% by weight with respect to the resin constituting the polyester film, the film has scratch resistance and separation. In addition to moldability, moldability is also favorable, which is preferable. More preferably, it is 1.5 to 7.5% by weight. The pigment, dye, organic or inorganic particles can be used alone or in combination of two or more.

  The thickness of the polyester film is not particularly limited and is appropriately selected depending on the application and type, but is preferably 10 to 500 μm, more preferably 38 to 250 μm from the viewpoint of mechanical strength, handling properties, and the like. Most preferably, it is 75 to 150 μm. The polyester film may be a composite film obtained by coextrusion or a film obtained by bonding the obtained film by various methods.

(9) Formation method of resin layer (X) In this invention, the resin composition containing resin (A) and a melamine compound (B) is provided on a polyester film, it heats after that, resin ( It is preferable to form a resin layer (X) containing α). In particular, it is preferable to set the heating temperature to 150 ° C. or higher because the resin layer (X) having the structure of the formulas (1) to (3) can be efficiently formed. Thereby, it is possible to obtain a laminated film excellent in scratch resistance, oligomer precipitation suppression and mold release properties.

  When the resin composition containing the resin (A) and the melamine compound (B) is provided on the polyester film, a solvent may be used. That is, the resin (A) and the melamine compound (B) may be dissolved or dispersed in a solvent to form a coating solution, which may be applied to a polyester film. After the application, the solvent is dried, and the film on which the resin (α) is laminated can be obtained by heating. In particular, the heating temperature is preferably 150 ° C. or higher. In the present invention, it is preferable to use an aqueous solvent (E) as a solvent. By using an aqueous solvent, rapid evaporation of the solvent in the heating step can be suppressed, and not only a uniform resin layer (X) can be formed, but also the environmental load is excellent.

  Here, the aqueous solvent (E) is water or water and alcohols such as methanol, ethanol, isopropyl alcohol and butanol, ketones such as acetone and methyl ethyl ketone, and glycols such as ethylene glycol, diethylene glycol and propylene glycol. The organic solvent that is soluble is mixed at an arbitrary ratio.

  As a method for applying the resin composition to the polyester film, either an in-line coating method or an off-coating method can be used, but an in-line coating method is preferable. The in-line coating method is a method of applying in the process of manufacturing a polyester film. Specifically, it refers to a method of coating at any stage from melt extrusion of a polyester resin to biaxial stretching followed by heat treatment and winding up, and is generally substantially non-obtainable after melt extrusion and rapid cooling. Crystalline unstretched (unoriented) polyester film (A film), then uniaxially stretched (uniaxially oriented) polyester film (B film) stretched in the longitudinal direction, or biaxially before heat treatment stretched further in the width direction It is applied to any one of stretched (biaxially oriented) polyester film (C film).

  In the present invention, the resin composition is applied to any one of the A film and B film of the polyester film before crystal orientation is completed, the solvent is evaporated, and then the polyester film is uniaxially or biaxially. It is preferable to employ a method in which the resin layer (X) is provided while being stretched and heated to complete the crystal orientation of the polyester film. According to this method, the production of the polyester film, the application of the resin composition, the drying of the solvent, and the heating (that is, the formation of the resin layer (X)) can be performed at the same time. is there. Moreover, it is easy to make the thickness of the resin layer (X) thinner in order to perform stretching after coating.

  Especially, the method of apply | coating a resin composition to the film (B film) uniaxially stretched to the longitudinal direction, drying a solvent, and extending | stretching to the width direction after that, and heating to 150 degreeC or more is preferable. Compared to the method of biaxial stretching after applying to an unstretched film, the stretching process is less than once, so that the occurrence of defects and cracks in the resin layer (X) due to stretching can be suppressed.

  On the other hand, the off-line coating method is different from the film-forming process on the film after the A film is stretched uniaxially or biaxially and subjected to heat treatment to complete the crystal orientation of the polyester film, or the A film. This is a method of applying a resin composition in the process. In this invention, it is preferable to provide by the in-line coating method from the various advantages mentioned above.

  Therefore, the best method for forming the resin layer (X) in the present invention is to apply a resin composition using an aqueous solvent (E) on a polyester film using an in-line coating method, and dry the aqueous solvent (E). And forming by heating.

(10) Adjustment method of coating liquid containing resin composition When preparing the coating liquid containing a resin composition, it is preferable to use an aqueous solvent (E) as a solvent. The coating liquid containing the resin composition is mixed and stirred in the desired weight ratio of the resin (A), the melamine compound (B), and the aqueous solvent (E), which are dispersed in water or water as necessary, in any order. Can be produced. Then, if necessary, various additives such as lubricants, inorganic particles, organic particles, surfactants, antioxidants, thermal initiators, etc., in a range that does not deteriorate the characteristics of the resin layer (X) provided by the resin composition. Mixing and stirring can be performed in any order. The mixing and stirring methods can be performed by shaking the container by hand, using a magnetic stirrer or stirring blade, irradiating ultrasonic waves, vibrating and dispersing.

(11) Coating method As a coating method of the resin composition on the thermoplastic resin film, a known coating method such as a bar coating method, a reverse coating method, a gravure coating method, a die coating method, or a blade coating method is used. be able to.

(12) Laminated film manufacturing method The manufacturing method of the laminated film of this invention is demonstrated. A polyethylene terephthalate (hereinafter abbreviated as PET) film is first sufficiently dried in vacuum with PET pellets to which pigments, dyes, organic or inorganic particles are added, if necessary, and then supplied to an extruder at about 280 ° C. And then melt-extruded into a sheet and cooled and solidified to produce an unstretched (unoriented) PET film (A film). This film is stretched 2.5 to 5.0 times in the longitudinal direction with a roll heated to 80 to 120 ° C. to obtain a uniaxially oriented PET film (B film). A coating solution having a resin composition containing a resin (A) and a melamine compound (B), prepared to a predetermined concentration, is applied to one side of the B film. At this time, surface treatment such as corona discharge treatment may be performed on the coated surface of the PET film before coating. By performing surface treatment such as corona discharge treatment, the wettability of the resin composition to the PET film can be improved, the repelling of the resin composition can be prevented, and a uniform coating thickness can be achieved.

  After coating, the edge of the PET film is held with a clip and guided to a preheating zone of 80 to 130 ° C., and the solvent of the coating solution is dried. After drying, the film is stretched 1.1 to 5.0 times in the width direction. Subsequently, it is guided to a heat treatment zone at 150 to 250 ° C., and heat treatment is performed for 1 to 30 seconds to complete the crystal orientation and the formation of the resin layer (X) containing the resin (α). In this heating step (heat treatment step), 3 to 15% relaxation treatment may be performed in the width direction or the longitudinal direction as necessary. The laminated film thus obtained is a release film that is excellent in suppressing oligomers against the oligomer that prevents scratches and precipitates from the polyester film in a processing step involving heat treatment.

(Characteristic measurement method and effect evaluation method)
The characteristic measuring method and the effect evaluating method in the present invention are as follows.

(1) Measurement of total light transmittance and haze Three points (three) of square-shaped laminated film samples each having a side of 5 cm are prepared. The sample is then allowed to stand for 40 hours in a normal state (23 ° C., relative humidity 50%). Each sample was measured with a turbidimeter “NDH5000” manufactured by Nippon Denshoku Industries Co., Ltd., and the total light transmittance was measured according to JIS “Testing method of total light transmittance of plastic transparent material” (K7361-1, 1997 edition). ), Haze is measured by a method according to JIS “How to Obtain Haze of Transparent Materials” (K7136, 2000 edition). The total light transmittance and haze value of each of the three points (three) are averaged to obtain the total light transmittance and haze value of the laminated film.

(2) Measurement of resin layer (X) thickness The laminated film is dyed with RuO ₄ . Next, the laminated film is frozen and cut in the film thickness direction to obtain 10 (10) ultra-thin slice samples for observing the cross section of the resin layer (X). Each sample cross section is observed with a TEM (transmission electron microscope: H7100FA type manufactured by Hitachi, Ltd.) at a magnification of 10,000 to 1,000,000 to obtain a cross-sectional photograph. The measured values of the resin layer (X) thickness of the 10 samples (10 pieces) are averaged to obtain the resin layer (X) thickness of the laminated film.

(3) Measurement of glass transition temperature (Tg) of resin (α) 5 mg of the laminated film is weighed. Next, the laminated film weighed was measured with a temperature modulation differential scanning calorimeter (TMDSC) Q1000 (manufactured by TA Instruments). In a temperature-modulated differential scanning calorimeter, the entire DSC signal (total heat flow) is separated into a reversible thermal component that generates heat and endotherm, such as glass transition, and an irreversible thermal component, such as enthalpy relaxation, curing reaction, and solvent removal. it can. A signal derived from the glass transition point of the resin (α), which is a reversible component, is separated and extracted from the entire differential scanning calorimetric signal obtained by the measurement to obtain the glass transition point of the resin (α). Here, it can distinguish from the glass transition point of resin ((alpha)) by measuring in advance the glass transition point of the polyester film which is a base film of a laminated | multilayer film.

(4) Calculation of surface free energy of resin layer (X) The laminated film was allowed to stand for 24 hours in an atmosphere having a room temperature of 23 ° C and a relative humidity of 65%. Thereafter, the contact angle of each of the four types of solutions of pure water, ethylene glycol, formamide, and diiodomethane with respect to the resin layer (X) side surface of the laminated film in the same atmosphere is a contact angle meter CA-D type ( 5 points each by Kyowa Interface Science Co., Ltd. The average value of the three measured values excluding the maximum value and the minimum value of the five measured values is defined as the contact angle of each solution.

Next, using the contact angles of the four types of solutions obtained, “the surface free energy (γ) of the solid, which is proposed by Hata et al., Is expressed as a dispersion force component (γ _S ^d ) and a polar force component (γ _S ^p ). , And the hydrogen bonding force component (γ _S ^h ), and the geometric mean method based on the formula (expanded Fowkes formula) obtained by extending the Fowkes formula, The surface energy that is the sum of the polar forces is calculated.

A specific calculation method is shown. The meaning of each symbol is described below. When γ _S ^L is the tension at the interface between the solid and the liquid, Equation (1) is established.

γ _S ^L : surface free energy of resin layer (X) and known solutions listed in Table 1 γ _S : surface free energy of resin layer (X) γ _L : surface free energy of known solutions listed in Table 1 γ _S ^d :
(Dispersive force component of surface free energy of X (X) γ _S ^p : Polar force component of surface free energy of resin layer (X) γ _S ^h : Hydrogen bond force component of surface free energy of resin layer (X) γ _L ^d : Dispersion force component of the surface free energy of the known solution described in Table 1 γ _L ^p : Polar force component of the surface free energy of the known solution described in Table 1 γ _L ^h : Known solution of the table 1 Γ _S ^L = γ _S + γ _L -2 (γ _S ^d · γ _L ^d ) ^1/2 -2 (γ _S ^p · γ _L p) ^1/2 -2 (γ _S ^h · γ _L ^h ) ^1/2 Formula (1).

  The state when the smooth solid surface and the droplet are in contact with each other at the contact angle (θ) is expressed by the following equation (Young's equation).

γ _S = γ _S ^L + γ _L cos θ (2)

When these mathematical formulas (1) and (2) are combined, the following formula is obtained.
_{^{(γ S d · γ L d}} ) 1/2 + (γ S p · γ L p) 1/2 + (γ S h · γ L h) 1/2 = γ L (1 + cosθ) / 2 ··· formula (3).

Actually, the four components of water, ethylene glycol, formamide, and diiodomethane have contact angles (θ) and the components of the surface tension of known solutions listed in Table 1 (γ _L ^d , γ _L ^p , γ _L ^h ) is substituted into Equation (3) to solve the four simultaneous equations. As a result, the surface free energy (γ) of the solid, that is, the surface free energy of the surface of the resin layer (X) is calculated.

(5) Measurement of pencil hardness of resin layer (X) Using HEIDON (manufactured by Shinto Kagaku Co., Ltd.), the resin film (X) side surface of the laminated film is installed so that pencils of different hardnesses are in contact with each other. Next, in accordance with JIS “Scratch hardness (pencil method)” (K5600-5-4, 2008 edition), the pencil is moved at a load of 750 g, a speed of 30 mm / min, and a moving distance of 10 mm. The measurement is performed by sequentially increasing the hardness of the pencil until a scratch mark having a length of 3 mm or more is generated on the resin layer (X) side surface of the laminated film. The pencil hardness of the resin layer (X) is defined as the hardness of the pencil before the scratch marks are formed on the resin layer (X) side surface of the laminated film.

(6) Scratch inhibition evaluation (abrasion test evaluation)
It fixes to a plane so that the resin layer (X) surface of a laminated film may become an upper surface. Next, using a stainless steel metal rod (SUS304, length 10 cm, diameter 1 cm), applying a constant load of 100 g to the surface of the resin layer (X), rotating the distance 10 cm straight at a speed of 10 cm / s without rotating. Rub on. The rubbed portion was observed with an optical microscope at a magnification of 100 to 500 times, and a rubbing scratch having a short side width of 20 μm was determined to be 5 or less.
◯: There are 5 or less scratches with a short side width of 20 μm or more on the surface of the resin layer (X).
Δ: 6 to 10 scratches with a short side width of 20 μm or more on the surface of the resin layer (X).
X: There are 11 or more scratches with a short side width of 20 μm or more on the surface of the resin layer (X).

(7) Evaluation of oligomer precipitation inhibition (heat treatment evaluation)
A laminated film sample having a side of 10 cm is fixed to a metal frame at four sides. Next, in the hot air oven “HIGH-TEMP-OVEN PHH-200” manufactured by ESPEC Co., Ltd., in which the laminated film sample fixed to the metal frame is set to 150 ° C. (air flow gauge “7”), the floor in the oven It was put up and heated for 1 hour, and then allowed to stand for 1 hour with air cooling. The surface of the polyester film opposite to the resin layer (X) is wiped off with a non-woven fabric containing acetone (manufactured by Ozu Sangyo Co., Ltd., Hyze Gauze NT-4), further rinsed with acetone, and allowed to dry for 40 hours in a normal state. The oligomer deposited from the polyester film surface opposite to the resin layer (X) was removed. Thereafter, the haze was measured in the same manner as in (1), and the difference from the haze before the heat treatment evaluation was evaluated as Δhaze. Δhaze of less than 0.3% was considered good. As a guide, if the Δhaze is less than 0.3%, the change in haze value is not visually recognized before and after the heat treatment. If it is 0.3% or more and less than 0.5%, there is an individual difference, but there is a possibility that a change in the haze value visually observed before and after the heat treatment. If it is 0.5% or more, a change in haze visually can be clearly seen before and after the heat treatment.

(8) Structure confirmation of formula (1)-(3) in resin layer (X) The confirmation method of the structure of formula (1)-(3) in resin layer (X) is not specifically limited to a specific method. However, the following method can be illustrated. For example, the presence or absence of a weight peak derived from the structure of formulas (1) to (3) is confirmed by gas chromatograph mass spectrometry (GC-MS). Next, the presence or absence of a peak derived from the bond between atoms of the structures of formulas (1) to (3) is confirmed by Fourier transform infrared spectroscopy (FT-IR). Furthermore, in proton nuclear magnetic resonance spectroscopy (1H-NMR), the position of the chemical shift derived from the position of the hydrogen atom and the number of proton absorption lines derived from the number of hydrogen atoms in the structures of formulas (1) to (3) Confirm. A method of comprehensively confirming these results is preferable.

(9) Release property evaluation Release property evaluation evaluated the cured film of the coating agent formed by apply | coating and hardening various coating agents to the resin layer (X) side surface of a laminated film by the cross-cut method. .
Coating agent A: Completely saponified polyvinyl alcohol (degree of saponification: 98 to 99 mol%) “PVA-117” (manufactured by Kuraray Co., Ltd.) 50% aqueous solution coating agent B: Organic solvent type UV curable hard coat ((Co., Ltd.) ) "Opstar" (registered trademark) KZ6445A manufactured by JSR)
Coating C: Solventless UV curable hard coat (adjusted with the following composition ratio)
• Sanyo Chemical Co., Ltd. “Sunrad” (registered trademark) RC-610: 60 parts by weight • Mitsubishi Rayon Co., Ltd. “Diabeam” (registered trademark) UR-6530: 20 parts by weight • Nippon Kayaku Co., Ltd. DPHA (dipentaerythritol pentaacrylate / dipentaerythritol hexaacrylate mixture): 20 parts by weight.

  About the coating agent A, it apply | coated to the surface of the resin layer (X) of a laminated film so that the film thickness after hardening may be set to 20 micrometers using a bar coater, and the hot air oven "HIGH-TEMP-OVEN" made by Espec Co., Ltd. The coating A layer was cured by drying at 100 ° C. for 5 minutes using “PHH-200”.

About the coating agent B, it apply | coated to the surface of the resin layer (X) of laminated | multilayer film so that the film thickness after hardening may be 20 micrometers using a bar coater, and the hot air oven "HIGH-TEMP-OVEN" made by Espec Co., Ltd. PHH-200 "was dried at 100 ° C for 5 minutes, and then an ultraviolet lamp with an irradiation intensity of 120 W / cm was used, the irradiation distance (distance between the lamp and the ink surface) was 12 cm, the conveyor speed was 3 m / min, and the integrated intensity was about 350 mJ / UV coating was applied at cm ² to cure the coating material C layer.

About the coating agent C, it apply | coated to the surface of the resin layer (X) of a laminated film so that the film thickness after hardening may be set to about 20 micrometers using an applicator, and it uses an ultraviolet lamp with irradiation intensity of 120 W / cm after that. The coating material D was cured by UV irradiation at an irradiation distance (distance between the lamp and the ink surface) of 12 cm, a conveyor speed of 2 m / min, and an integrated intensity of about 550 mJ / cm ² .

<Cross-cut method evaluation conditions>
Put 100 crosscut of 1 mm ² to the cured film of various coating agents, paste Nichiban Co., Ltd. "cellophane tape" (registered trademark) thereon, using a rubber roller, 3 shuttled load 19.6N And then peeled off in the direction of 90 degrees, and evaluated by the number of remaining cured films. The remaining number is 5 or less as good releasability, and from 6 to 20 is releasability. Slightly poor “Δ” and 21 or more were defined as poor releasability “x”.

Example 1
Resin having a hydroxyl group and an acryloyl group (A):
In a stainless steel reaction vessel, methyl methacrylate (a), hydroxyethyl methacrylate (b), urethane acrylate oligomer (manufactured by Negami Kogyo Co., Ltd., Art Resin (registered trademark) UN-3320HA, the number of acryloyl groups is 6) (c ) Was added at a mass ratio in the table, and 2 parts by mass of sodium dodecylbenzenesulfonate as an emulsifier was added to a total of 100 parts by mass of (a) to (c) and stirred to prepare a mixed solution 1. Next, a reactor equipped with a stirrer, a reflux condenser, a thermometer, and a dropping funnel was prepared. 60 parts by weight of the above mixed liquid 1, 200 parts by weight of isopropyl alcohol, and 5 parts by weight of potassium persulfate as a polymerization initiator were charged into a reactor and heated to 60 ° C. to prepare a mixed liquid 2. The mixed liquid 2 was held for 20 minutes while being heated at 60 ° C. Next, a mixed solution 3 composed of 40 parts by weight of the mixed solution 1, 50 parts by weight of isopropyl alcohol, and 5 parts by weight of potassium persulfate was prepared. Subsequently, the mixed solution 3 was dropped into the mixed solution 2 using a dropping funnel over 2 hours to prepare the mixed solution 4. Thereafter, the mixed solution 4 was kept for 2 hours while being heated to 60 ° C. The obtained mixed liquid 4 was cooled to 50 ° C. or lower and then transferred to a container equipped with a stirrer and a decompression facility. Thereto, 60 parts by weight of 25% aqueous ammonia and 900 parts by weight of pure water were added, and isopropyl alcohol and unreacted monomers were recovered under reduced pressure while heating to 60 ° C., and resin (A) dispersed in pure water Got.

Melamine compound having a methylol group (B):
Methylolated melamine (manufactured by Sanwa Chemical Co., Ltd., Nicalac (registered trademark) MW-035) was used.

-Resin composition and coating liquid containing resin composition:
The resin (A) and the melamine compound (B) were mixed in a mass ratio such that (A) / (B) = 100/50. In order to impart easy slipping to the surface of the laminated film, silica particles having a number average particle size of 300 nm (Seahoster (registered trademark) KE-W30 manufactured by Nippon Shokubai Co., Ltd.) as resin particles (A) 100 are used. 2 parts by mass was added to parts by mass. Further, in order to improve the coating property of the resin composition on the polyester film, a fluorosurfactant (Plus Coat (registered trademark) RY-2 manufactured by Kyoyo Chemical Co., Ltd.) and a coating liquid containing the resin composition are used. It added so that content with respect to might become 0.06 mass part.

・ Polyester film:
PET pellets (intrinsic viscosity 0.64 dl / g) containing two types of particles (4% by weight of silica particles with a primary particle size of 0.3 μm and 2% by weight of calcium carbonate particles with a primary particle size of 0.8 μm) Is sufficiently dried in a vacuum, supplied to an extruder, melted at 285 ° C., extruded into a sheet form from a T-shaped die, wound around a mirror casting drum having a surface temperature of 25 ° C. using an electrostatic application casting method, and cooled and solidified. I was damned. This unstretched film was heated to 90 ° C. and stretched 3.1 times in the longitudinal direction to obtain a uniaxially stretched film (B film).

・ Laminated film:
The resin composition was applied to a uniaxially stretched film with a coating thickness of about 6 μm using a bar coat. Subsequently, both end portions in the width direction of the uniaxially stretched film coated with the resin composition were held with clips and led to the preheating zone. The atmospheric temperature of the preheating zone was set to 90 ° C. to 100 ° C., and the solvent of the coating liquid containing the resin composition was dried. Subsequently, the film is continuously stretched 3.7 times in the width direction in a stretching zone at 100 ° C., followed by heat treatment for 20 seconds in a heat treatment zone at 235 ° C. to form a resin (α), and the crystal orientation of the polyester film is completed. A laminated film was obtained. In the obtained laminated film, the thickness of the PET film was 100 μm, and the thickness of the resin layer (X) was about 85 nm.

  About resin layer (X) of a laminated | multilayer film, presence of the weight peak derived from the structure of Formula (1)-(3) was confirmed by gas chromatograph mass spectrometry (GC-MS). Next, the presence of peaks derived from the bonds between the atoms of the structures of the formulas (1) to (3) was confirmed by Fourier transform infrared spectroscopy (FT-IR). Finally, in proton nuclear magnetic resonance spectroscopy (1H-NMR), the number of hydrogen atoms is calculated from the position of the chemical shift derived from the position of the hydrogen atom in the structures of formulas (1) to (3) and the proton absorption line area. confirmed. By combining these results, it was confirmed that the resin layer (X) had the structures of the formulas (1) to (3).

  The characteristics of the obtained laminated film are shown in the table. Scratch inhibition was “good”, releasability was “good”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%.

(Example 2)
A laminated film was obtained in the same manner as in Example 1 except that the particles contained in the polyester film were changed to 2% by weight of silica particles having a primary particle size of 2.6 μm. The characteristics of the obtained laminated film are shown in the table. Scratch inhibition was “good”, releasability was “good”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%.

(Example 3)
A laminated film was obtained in the same manner as in Example 1 except that the particles contained in the polyester film were changed to 2% by weight of silica particles having a primary particle size of 0.3 μm. The characteristics of the obtained laminated film are shown in the table. Scratch inhibition was “good”, releasability was “good”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%.

(Examples 4 and 5)
A laminated film was obtained in the same manner as in Example 1 except that the coating thickness of the resin composition by bar coating on the uniaxially stretched film was changed and the thickness of the resin layer (X) was changed to the thickness described in the table. The characteristics of the obtained laminated film are shown in the table. Scratch inhibition was “good”, releasability was “good”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%. It is considered that the pencil hardness is improved by increasing the thickness of the resin layer (X).

(Examples 6 and 7)
A laminated film was obtained in the same manner as in Example 1 except that the mass ratio of the resin (A) was changed to the mass ratio shown in the table. The characteristics of the obtained laminated film are shown in the table. In Examples 8 and 9 in which the composition of the resin (A) having an acrylate structure is changed as compared with Example 2, the pencil hardness is F or more, the scratch inhibiting property is “◯”, the releasability is “◯”, and The haze change after heat treatment at 150 ° C. for 1 hour was a good result within 0.3%.

(Examples 8 and 9)
A laminated film was obtained in the same manner as in Example 1 except that the mass ratio of the resin (A) and the melamine compound (B) was changed to the mass ratio described in the table. The characteristics of the obtained laminated film are shown in the table. In Examples 8 and 9 in which the mass ratio of the melamine compound (B) was changed as compared with Example 4, the pencil hardness was F or more, the scratch resistance was “O”, the release property was “O”, and 150 The haze change after the heat treatment at 1 ° C. for 1 hour was a good result within 0.3%.

(Examples 10 and 11)
As a component other than the resin (A) and the melamine compound (B) in the resin layer (X), the mass described in the table with respect to 100 parts by mass of the resin (A) of 2-vinyl-2-oxazoline (C) A laminated film was obtained in the same manner as in Example 1 except that the part was added. The characteristics of the obtained laminated film are shown in the table. In Examples 10 and 11 in which the mass ratio of the resin (A), the melamine compound (B), and the compound having an oxazoline group (C) in the resin layer (X) is changed as compared with Example 1, the damage is suppressed. As a result, the property was good, and the change in haze after heat treatment at 150 ° C. for 1 hour was within 0.3%.

(Examples 12 to 14)
In the production process of the laminated film, a laminated film was obtained in the same manner as in Example 1 except that the heating temperature in the heat treatment zone after stretching was changed to the temperature described in the table. The characteristics of the obtained laminated film are shown in the table. In Examples 12 to 14 in which the heat treatment temperature was changed as compared with Example 2, scratch resistance was “◯”, release property was “◯”, and haze change after heat treatment at 150 ° C. for 1 hour was 0. It was a good result within 3%.

(Example 15)
Compound (c) in resin (A) is urethane acrylate oligomer (manufactured by Negami Kogyo Co., Ltd., Art Resin (registered trademark) UN-3320HA, number of acryloyl groups is 6), 5 parts by mass, and N-methylolacrylamide A laminated film was obtained in the same manner as in Example 1 except that the compound was obtained by polymerizing 5 parts by mass (a compound having a urethane structure and a polyfunctional acryloyl group). The characteristics of the obtained laminated film are shown in the table. In Example 15 in which the composition of the compound (c) was changed as compared with Example 1, the scratch resistance was “◯”, the releasability was “O”, and the haze change after heat treatment at 150 ° C. for 1 hour was observed. It was a good result within 0.3%.

(Example 16)
Compound (c) in resin (A) is converted into a urethane acrylate oligomer (manufactured by Toyo Chemicals Co., Ltd., Miramer (registered trademark) HR3200, the number of acryloyl groups is 4) (a compound having a urethane structure and a polyfunctional acryloyl group). A laminated film was obtained in the same manner as in Example 1 except for the change. The characteristics of the obtained laminated film are shown in the table. In Example 14 in which the composition of the compound (c) was changed as compared with Example 1, the scratch resistance was “◯”, the releasability was “O”, and the haze change after heat treatment at 150 ° C. for 1 hour. It was a good result within 0.3%.

(Example 17)
Compound (c) in resin (A) is urethane acrylate oligomer (manufactured by Negami Kogyo Co., Ltd., Art Resin (registered trademark) UN-3320HS, number of acryloyl groups is 15) (having urethane structure and polyfunctional acryloyl group) A laminated film was obtained in the same manner as in Example 1 except that the compound was changed to (Compound). The characteristics of the obtained laminated film are shown in the table. In Example 17, in which the composition of the compound (c) was changed as compared with Example 1, the scratch inhibiting property was “◯”, the releasability was “◯”, and the haze change after heat treatment at 150 ° C. for 1 hour was observed. It was a good result within 0.3%.

(Example 18)
A laminated film was obtained in the same manner as in Example 17 except that the mass ratio of the resin (A) and the melamine compound (B) was changed to the mass ratio described in the table. The characteristics of the obtained laminated film are shown in the table. In Example 18 in which the mass ratio of the melamine compound (B) was changed as compared with Example 17, the scratch inhibiting property was “◯”, the releasability was “O”, and haze after heat treatment at 150 ° C. for 1 hour. The change was as good as within 0.3%.

(Example 19)
A laminated film was obtained in the same manner as in Example 1 except that the ethylenically unsaturated compound (b) having a hydroxyl group in the resin (A) was changed to 2-hydroxyethyl acrylate. The characteristics of the obtained laminated film are shown in the table. In Example 19, in which the ethylenically unsaturated compound (b) having a hydroxyl group was changed as compared with Example 1, the scratch inhibiting property was “◯”, the releasability was “◯”, and heat treatment at 150 ° C. for 1 hour. The haze change afterwards was a good result within 0.3%.

(Example 20)
A laminated film was obtained in the same manner as in Example 1 except that the mass ratio of the resin (A) was changed to the mass ratio shown in the table. The characteristics of the obtained laminated film are shown in the table. The resin layer (X) of the laminated film was analyzed by GC-MS, FT-IR, and 1H-NMR. As a result, it was confirmed that the resin layer (X) had the structures of formulas (1) and (2). The structure of (3) was not confirmed. In Example 20 where there is no compound (c) having a chemical structure (urethane structure) represented by formula (3) and a polyfunctional acryloyl group in the resin (A), cracks occurred in the resin layer (X). Compared with 2, the haze increased, but the scratch resistance was “◯”, the releasability was “◯”, and the haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%. there were.

(Example 21)
In the resin composition, as a component other than the resin (A) and the melamine compound (B), a release agent (D) composed of the following long-chain alkyl group-containing acrylic resin is added to 100 parts by mass of the resin (A). A laminated film was obtained in the same manner as in Example 1 except that the parts by mass described in the table were added. The characteristics of the obtained laminated film are shown in the table.
Release agent (D): 500 parts by weight of toluene, 65 parts by weight of stearyl methacrylate (carbon number of alkyl chain 18), 25 parts by weight of methacrylic acid in a temperature-adjustable reactor equipped with a stirrer, a thermometer, and a condenser Then, 10 parts by weight of 2-hydroxyethyl methacrylate and 1 part of azobisisobutyronitrile were placed in a dropping device and dropped at a reaction temperature of 85 ° C. over 4 hours to carry out a polymerization reaction. Thereafter, the reaction was completed by aging at the same temperature for 2 hours to obtain a compound as a release agent (D). A resin composition in which the obtained compound is dissolved in water containing 5% by weight of isopropyl alcohol and 5% by weight of n-butyl cellosolve, a solution containing a release agent (D) is prepared, and a resin layer (X) is formed. Added to the containing coating solution.

  Compared with Example 1, the surface free energy of the resin layer (X) decreased as an effect of the release agent (D). Scratch inhibition was “good”, releasability was “good”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%.

(Examples 22 and 23)
A laminated film was obtained in the same manner as in Example 21, except that the amount of the release agent (D) added was changed as described in the table. The characteristics of the obtained laminated film are shown in the table. Compared with Example 21, the surface free energy of the resin layer (X) further decreased. Scratch inhibition was “good”, releasability was “good”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%.

(Example 24)
As a component other than the resin (A) and the melamine compound (B) in the resin composition, the following carnauba wax release agent as a mold release agent is shown in parts by mass with respect to 100 parts by mass of the resin (A). A laminated film was obtained in the same manner as in Example 1 except that was added. The characteristics of the obtained laminated film are shown in the table.

-Carnauba wax release agent: Cerozol 524 (manufactured by Chukyo Yushi Co., Ltd.)
Compared with Example 1, the surface free energy of the resin layer (X) decreased as an effect of the release agent (D). Pencil hardness was “HB”, but the effect of the release agent was to prevent scratching, “○”, release property was “◯”, and haze change after heat treatment at 150 ° C. for 1 hour was within 0.3% And good results.

(Comparative Example 1)
A laminated film was obtained in the same manner as in Example 1 except that the thickness of the resin layer (X) was changed to the thickness described in the table. The characteristics of the obtained laminated film are shown in the table. When the thickness of the resin layer (X) was reduced as compared with Example 1, the releasability was good, but the scratch resistance and haze change after heat treatment at 150 ° C. for 1 hour were poor.

(Comparative Examples 2 to 4)
A laminated film was obtained in the same manner as in Example 1 except that the mass ratio of the resin (A) was changed to the mass ratio shown in the table. The characteristics of the obtained laminated film are shown in the table. In Comparative Examples 3 to 5 in which the composition of the resin (A) having an acrylate structure is changed as compared with Example 1, both the scratch inhibition property, the releasability evaluation, and the haze change after heat treatment at 150 ° C. for 1 hour. It was bad.

(Comparative Example 5)
A laminated film was obtained in the same manner as in Example 1 except that the mass ratio of the resin (A) was changed to the mass ratio shown in the table. In Comparative Example 5 where there is no ethylenically unsaturated compound (b) having a hydroxyl group in the resin (A), it was impossible to disperse the resin composition in an aqueous solvent. What was made to use was used. The characteristics of the obtained laminated film are shown in the table. In Comparative Example 5, the scratch inhibiting property, the release property evaluation, and the haze change after the heat treatment at 150 ° C. for 1 hour were unsatisfactory. The resin layer (X) of the laminated film was analyzed by GC-MS, FT-IR, and 1H-NMR. As a result, it was confirmed that the resin layer (X) had the structures of formulas (2) and (3). The structure of (1) was not confirmed.

(Comparative Example 6)
Resin composition in which 32% by mass of oxazoline compound (C) (“Epocross” WS-500 manufactured by Nippon Shokubai Co., Ltd.) is added to the resin layer (X) so that the resin (α) content is 68% by mass. A laminated film was obtained in the same manner as in Example 1 except that the product was adjusted. The characteristics of the obtained laminated film are shown in the table. In Comparative Example 6 in which the content of the resin (α) was reduced as compared with the Examples, the scratch resistance, the release property evaluation, and the haze change after heat treatment at 150 ° C. for 1 hour were poor.

(Comparative Example 7)
A laminated film was obtained in the same manner as in Example 1 except that the mass ratio of the resin (A) was changed to the mass ratio shown in the table. The characteristics of the obtained laminated film are shown in the table. In Comparative Example 7 in which the mass ratio of the resin (A) and the melamine compound (B) in the resin layer (X) was changed as compared to Example 1, scratch resistance, release evaluation, and 150 ° C. for 1 hour Both haze changes after heat treatment were poor.

(Comparative Example 8)
A laminated film was obtained in the same manner as in Example 1 except that the polyester film did not substantially contain particles. The characteristics of the obtained laminated film are shown in the table. Scratch inhibition was “◯” and the haze change after heat treatment at 150 ° C. for 1 hour was within 0.3%, but the releasability was “x” to “△”, and the releasability was poor. It was.

(Comparative Example 9)
A laminated film was obtained in the same manner as in Example 21, except that the amount of the release agent (D) added was changed as described in the table. The characteristics of the obtained laminated film are shown in the table. Compared with Example 21, the surface free energy of the resin layer (X) further decreased. Scratch inhibition was “◯” and releasability was “◯”, but the haze change after heat treatment at 150 ° C. for 1 hour was 0.3% or more, resulting in failure.

  The present invention is a resin layer that suppresses scratches on the film surface that occur in the process of film formation and conveyance of a polyester film, suppresses oligomers that precipitate from the polyester film in a processing step involving heat treatment, and is excellent in releasability. It can be used for a release film such as a polarizing plate release application.

Claims (20)

A laminated film in which a resin layer (X) using a resin (α) is provided on at least one surface of a polyester film, which satisfies the following conditions (1) to (5).
(1) The thickness of the resin layer (X) is 80 nm or more. (2) The resin (α) is a resin having a glass transition temperature of 50 ° C. or more. (3) Surface free energy of the resin layer (X) (4) The resin (α) is obtained from a resin composition containing a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group. (5) The haze of the laminated film is greater than 3.0% The laminated film according to claim 1, wherein the resin layer (X) has a pencil hardness of “F” or more. The laminated film according to claim 1 or 2, wherein the resin forming the resin layer (X) has a chemical structure represented by the formula (1).

The laminated film according to any one of claims 1 to 3, wherein the resin forming the resin layer (X) has a chemical structure represented by the formula (2).

The laminated film according to any one of claims 1 to 4, further comprising a release agent in the resin composition forming the resin layer (X). A laminated film in which a resin layer (X) using a resin (α) is provided on at least one surface of a polyester film, which satisfies the following conditions (1) to (5).
(1) The thickness of the resin layer (X) is 80 nm or more. (2) The resin (α) is a resin having a glass transition temperature of 50 ° C. or more. (3) Surface free energy of the resin layer (X) 40 mN / m or more and less than 50 mN / m (4) The resin forming the resin layer (X) has a crosslinked structure of acryloyl groups, a chemical structure represented by the formula (1), and a formula (2) (5) The haze of the laminated film is greater than 3.0%

The laminated film according to claim 6, wherein the resin layer (X) has a pencil hardness of “F” or more. The laminated film according to claim 6 or 7, wherein a release agent is contained in the resin composition forming the resin layer (X). The laminated film according to any one of claims 1 to 8, wherein the resin forming the resin layer (X) has a chemical structure represented by the formula (3).

The laminated film according to any one of claims 1 to 9, which is used as a release film. A method for producing a laminated film satisfying the following conditions (1) to (4), wherein a resin layer (X) is provided on at least one surface of a polyester film,
A resin composition comprising a resin (A) having a hydroxyl group and an acryloyl group and a melamine compound (B) having a methylol group is applied to at least one surface of the polyester film, and the applied resin composition is heated to 150 ° C. or higher. The manufacturing method of a laminated | multilayer film including the process of forming the resin layer (X) which consists of resin ((alpha)) obtained by doing.
(1) The thickness of the resin layer (X) is 80 nm or more. (2) The resin (α) is a resin having a glass transition temperature of 50 ° C. or more. (3) Surface free energy of the resin layer (X) 40 mN / m or more and less than 50 mN / m (4) The haze of the laminated film is greater than 3.0% The method for producing a laminated film according to claim 11, wherein the resin layer (X) has a pencil hardness of “F” or more. The total content of the resin (A) having a hydroxyl group and an acryloyl group and the melamine compound (B) having a methylol group in the resin composition is 70% by mass or more based on the solid content in the resin composition. The manufacturing method of the laminated | multilayer film of Claim 11 or 12. In the resin composition, the mass ratio of the content of the resin (A) and the melamine compound (B) (the content of the resin (A) [parts by mass] / the content of the melamine compound (B) [parts by mass]). The manufacturing method of the laminated | multilayer film in any one of Claims 11-13 which are 100 / 30-100 / 100. The method for producing a laminated film according to any one of claims 11 to 14, wherein the resin (A) further has a chemical structure (urethane structure) represented by the formula (3).

The resin (A) is a resin obtained by polymerization using at least the following compounds (a) to (c), and the mass ratio of each compound used is as follows. The manufacturing method of the laminated film in any one.
-Acrylic ester compound and / or methacrylic ester compound (a): 55-98 parts by mass-Ethylenically unsaturated compound having a hydroxyl group (b): 1-30 parts by mass-Chemical structure represented by formula (3) ( (Urethane structure) and compound (c) having a polyfunctional acryloyl group: 1 to 15 parts by mass The total mass of (a) to (c) is 100 parts by mass.

The method for producing a laminated film according to claim 16, wherein the compound (c) further has a methylol group. In the resin composition, the mass ratio of the content of the resin (A) and the release agent (the content of the resin (A) [parts by mass] / the content of the release agents [parts by mass]) is 100/5. It is -100/30. The manufacturing method of the laminated | multilayer film in any one of Claims 11-17. The resin composition is applied to at least one surface of a polyester film, then stretched in at least a uniaxial direction, and then heated to 150 ° C or higher to form a resin layer (X). A method for producing a laminated film. The method for producing a laminated film according to claim 11, wherein the laminated film is used as a release film.