JP5922506B2 - Transparent resin film - Google Patents

Description

  The present invention relates to a transparent resin film, and more particularly to a transparent resin film having high flexibility and excellent surface hardness and thermoformability.

A decorative molded body in which a decorative film provided with a design layer and a resin molded body are integrated is frequently used in a housing of an automobile interior, a home appliance, a small portable machine, or the like. By integrating the resin molded body and the decorative film from the design layer side of the decorative film, it is possible to obtain a molded body having a three-dimensional effect and a sense of depth. Moreover, the said decorative molded body has the advantage that there is no design layer deterioration by wear at the time of long-term use.
As a method of integrating the resin molded body and the decorative film, the decorative film is inserted into an injection mold without preforming, and a molten resin is injected there to form an injection molded body at the same time. A method of pasting a decorative film on a molded body, a decorative film is preformed by thermoforming (vacuum molding, pressure forming, vacuum pressure forming, etc.), then set in an injection mold, and molten resin there Is used to form an injection-molded body and at the same time to be integrated with a preformed decorative film.

Examples of the transparent film to be printed constituting the decorative film include a polycarbonate single layer film and an acrylic single layer film. Although the polycarbonate single layer film has high toughness and flexibility, there is a problem that the surface hardness is low and the surface of the molded body is easily damaged.
Although it has not been evaluated as a decorative film application, as a method for improving the surface hardness of a polycarbonate molded body, a method using a polycarbonate having a specific structural unit (Patent Document 1) or a polycarbonate and a specific (meta) The method of using the resin composition (patent document 2) which consists of an acrylate copolymer is mentioned.
On the other hand, acrylic single-layer film has high surface hardness and excellent scratch resistance, but it has low toughness and flexibility, making it difficult to mold the film, and causing breakage such as cracking during handling and transportation of the film. There is a problem that.
As a method for improving this problem, a film is proposed in which acrylic rubber particles are added to acrylic to increase flexibility (Patent Document 3).

As a method for achieving both flexibility and surface hardness, a laminated film of acrylic and polycarbonate has been proposed (Patent Document 4). By using a film having an acrylic surface as a molding surface and a polycarbonate surface as a printing surface, it is possible to have toughness and flexibility higher than that of an acrylic single layer film while maintaining the surface hardness of the acrylic surface.
However, the multilayer film may break when bent with the acrylic surface convex, and cannot be said to have sufficient toughness and flexibility. Since the acrylic layer thickness of a certain level or more is necessary for maintaining the hardness, the acrylic layer thickness / overall thickness ratio increases as the total film thickness decreases, and the above-described reductions in toughness and flexibility become significant.

JP-A 64-69625 JP 2010-116501 A Japanese Patent No. 3142774 JP 2006-316124 A

  An object of this invention is to provide the transparent resin film which has high flexibility and is excellent in surface hardness and thermoformability.

As a result of intensive studies to solve the above problems, the present inventors satisfy the above characteristics by using a film containing a resin composition comprising a specific polycarbonate and a specific (meth) acrylate copolymer. I found out.
That is, the present invention provides a transparent resin film having the following characteristics.

1. (Meth) acrylate copolymer (A) 15 to 55% by mass containing 5 to 80% by mass of aromatic (meth) acrylate (a1) and 20 to 95% by mass of methyl methacrylate (a2), and the following formula [1]
(In the formula [1], R is a single bond, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 10 carbon atoms, or a cyclic alkyl group having 3 to 8 carbon atoms, and X and Y are each independent. A resin composition comprising 85 to 45% by mass of a polycarbonate (B) containing a structural unit represented by a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and having an overall thickness of 300 μm or less. It is a film characterized by being.
2. The polycarbonate (B) is represented by the following formula [2]
0-100 mass% of the structural unit of the following formula [3]
The film according to 1 above, wherein the film is a polycarbonate homopolymer or copolymer containing 100 to 0% by mass of the structural unit.
3. 3. The film according to 2 above, wherein the polycarbonate (B) is a polycarbonate single polymer comprising the structural unit of the formula [3].
4). 4. The film according to any one of 1 to 3 above, wherein the film has a hard coat layer on one side or both sides and has a pencil hardness of 2H or more.
5. 3. A three-dimensional molded article having a pencil hardness of H or higher, which is formed by forming a design layer on one side of the film according to any one of the above 1 to 3 and then subjecting the film to pressure forming under heat and pressure.
6). 4. An in-mold molded product formed by forming a design layer on one surface of the film according to any one of 1 to 3 above and thermoforming the film, while forming a backing layer by injection molding a molten resin on the design layer side. It is.

  According to the present invention, a transparent resin film having high flexibility and excellent surface hardness and thermoformability is provided, and the transparent resin film of the present invention is suitably used for decorative film applications.

  Hereinafter, the present invention will be described in detail with reference to production examples and examples, but the present invention is not limited to the illustrated production examples and examples, and the scope of the present invention is not greatly deviated. If so, it can be changed to any method.

The present invention includes 15 to 55% by mass of (meth) acrylate copolymer (A) containing 5 to 80% by mass of aromatic (meth) acrylate (a1) and 20 to 95% by mass of methyl methacrylate (a2); Formula [1]
(In the formula [1], R is a single bond, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 10 carbon atoms, or a cyclic alkyl group having 3 to 8 carbon atoms, and X and Y are each independent. A resin composition comprising 85 to 45% by mass of a polycarbonate (B) containing a structural unit represented by a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and having an overall thickness of 300 μm or less. It is a film characterized by being.
Preferably, the film of this invention contains the resin composition which consists of 20-50 mass% of (meth) acrylate copolymers (A) and a polycarbonate (B) 80-50 mass%.

<(Meth) acrylate copolymer (A)>
The (meth) acrylate copolymer (A) used for the film of the present invention comprises 5 to 80% by mass of an aromatic (meth) acrylate unit (a1) and 20 to 95% by mass of a methyl methacrylate unit (a2) (meta ) Acrylate copolymer. Preferably, it is a (meth) acrylate copolymer comprising 10 to 70% by mass of aromatic (meth) acrylate units (a1) and 30 to 90% by mass of methyl methacrylate units (a2).

  The aromatic (meth) acrylate (a1) refers to a (meth) acrylate having an aromatic group in the ester moiety. Examples of the aromatic (meth) acrylate include phenyl (meth) acrylate and benzyl (meth) acrylate. These can be used alone or in combination of two or more. Of these, phenyl methacrylate and benzyl methacrylate are preferable, and phenyl methacrylate is more preferable. By having the aromatic (meth) acrylate unit (a1), the transparency of the molded body mixed with the polycarbonate (B) can be improved.

  The methyl methacrylate unit (a2) has an effect of being well dispersed with the polycarbonate resin and moves to the surface of the molded body, so that the surface hardness of the molded body can be improved.

  The (meth) acrylate copolymer (A) used in the present invention is a (meth) acrylate copolymer in which the weight ratio of (a1) and (a2) is 5 to 80/20 to 95. If the content of (a1) in the (meth) acrylate copolymer is 5% by mass or more, transparency is maintained in the high addition region of the (meth) acrylate copolymer (A), and the content is 80% by mass or less. If there is, the compatibility with the polycarbonate (B) is not too high, and the migration to the surface of the molded body does not decrease, so the surface hardness does not decrease.

  The (meth) acrylate copolymer (A) used by this invention can contain another structural unit (a3) as needed. (A3) is, for example, methacrylates such as ethyl methacrylate, butyl methacrylate, propyl methacrylate, and 2-ethylhexyl methacrylate; acrylates such as methyl acrylate, ethyl acrylate, butyl acrylate, propyl acrylate, 2-ethylhexyl acrylate, and glycidyl acrylate; acrylonitrile, methacrylate Vinyl cyanide monomers such as nitrile; Diene monomers such as butadiene, isoprene and dimethylbutadiene; Vinyl ether monomers such as vinyl methyl ether and vinyl ethyl ether; Carboxylic acids such as vinyl acetate and vinyl butyrate Vinyl monomer; Olefin monomer such as ethylene, propylene and isobutylene; Ethylene unsaturated such as acrylic acid, methacrylic acid, maleic acid and itaconic acid Rubonic acid monomer; vinyl halide monomers such as vinyl chloride and vinylidene chloride; maleimide monomers such as maleimide, N-phenylmaleimide, N-cyclohexylmaleimide, N-methylmaleimide; allyl (meth) acrylate, Examples of the crosslinking agent include divinylbenzene and 1,3-butylene dimethacrylate. Of these, preferred are methacrylate, acrylate, and vinyl cyanide monomer, and more preferred is acrylate from the viewpoint of suppressing thermal decomposition of the (meth) acrylate copolymer (A). These monomers can be used alone or in combination of two or more.

  When the other structural unit (a3) is contained, the (meth) acrylate copolymer (A) is an aromatic (meth) acrylate unit (a1) 5 to 79.9% by mass, a methyl methacrylate unit (a2) 20 to 20%. It is preferable to contain 94.9 mass% and 0.1-10 mass% of another structural unit (a3) (however, the sum total of (a1)-(a3) is 100 mass%).

  The weight average molecular weight of the (meth) acrylate copolymer (A) is preferably 5,000 to 30,000, and more preferably 10,000 to 25,000. When the weight average molecular weight is 5,000 to 30,000, the compatibility with the polycarbonate (B) is good, and the effect of improving the surface hardness is excellent. The weight average molecular weight (Mw), number average molecular weight (Mn), and molecular weight distribution (Mw / Mn) of the (meth) acrylate copolymer (A) are gel permeation chromatography using THF or chloroform as a solvent. Can be used to measure.

<Polycarbonate (B)>
The polycarbonate (B) used in the present invention is a polycarbonate containing the structural unit of the formula [1], and any single polymer or copolymer can be used as long as it is a polycarbonate containing the structural unit of the formula [1]. Is possible. As for the copolymer, in addition to the copolymer containing only the structural unit of the formula [1], a copolymer polycarbonate containing the formula [1] and the formula [3] in the structural unit can also be used. When using this copolymer, it is preferable that the ratio of the structural unit of Formula [3] used for a copolymer shall be 80 mass% or less.
As the formula [1], a structural unit of the following formula [2] is particularly preferred.

That is, in the present invention, the polycarbonate (B) is represented by the following formula [2].
0-100 mass% of the structural unit of the following formula [3]
The aspect which is a polycarbonate homopolymer or copolymer containing 100 to 0 mass% of the structural unit is preferable.

  In the present invention, the weight average molecular weight of the polycarbonate (B) is determined by the ease of mixing (dispersing) with the (meth) acrylate copolymer (A) and the ease of production. That is, if the weight average molecular weight of (B) is too large, the difference in melt viscosity between (A) and (B) becomes too large, so that the mixing (dispersion) of both becomes worse and the transparency of the film deteriorates, or There arises a problem that stable melt-kneading cannot be continued. On the other hand, when the weight average molecular weight of (B) is too small, there arises a problem that the impact resistance of the film is lowered. The weight average molecular weight of (B) is preferably in the range of 21,000 to 40,000, more preferably in the range of 24,000 to 38,000, and particularly preferably in the range of 27,000 to 36,000.

  The manufacturing method of the polycarbonate (B) used for this invention can be suitably selected with the monomers to be used, such as a well-known phosgene method (interfacial polymerization method) and transesterification method (melting method).

<About additives, etc.>
The film of the present invention may contain components other than the (meth) acrylate copolymer (A) and the polycarbonate (B) as necessary, as long as the effects of the present invention are not impaired. Components other than (A) and (B) include antioxidants, mold release agents, UV absorbers and the like.

<Film manufacturing method>
The film of the present invention is produced by melt extrusion. Specifically, after the (meth) acrylate copolymer (A) and the polycarbonate (B) are mixed in a powder state, they are pelletized by melt extrusion using a single screw extruder or a twin screw extruder, A manufacturing method in which pellets are formed into a film by melt extrusion using a single screw extruder or a twin screw extruder, or after mixing (A) and (B) in a powder state, a single screw extruder or a twin screw extruder And a production method of directly forming a film by melt extrusion.

The film of the present invention is usually produced by an extrusion method or a solution pouring method, and the thickness is appropriately selected from a range of 300 μm or less. The film of the present invention preferably has an overall thickness of 30 to 250 μm.
And you may perform a hard-coat process in an extrusion process or after being extruded. In the present invention, those excellent in abrasion resistance and fingerprint resistance (fingerprint wiping properties) are preferable, and those that can be processed into a desired shape by punching are particularly preferable from the viewpoint of productivity.

For the hard coat layer that can be formed on the film of the present invention, known compounds that form a crosslinked film such as acrylic, silicon, melamine, urethane, and epoxy can be used. As the curing method, a known method such as ultraviolet curing, thermal curing, electron beam curing or the like can be used. Among these, the surface to be the surface side is particularly preferably a pencil hardness of 2H or higher, or a steel wool hardness of 2 or higher, and is preferably exemplified by an acrylic type and a silicon type. From the balance, an acrylic type is preferable.
The hard coat layer may be applied by an ordinary method, such as a coating method such as a roll coating method, a dipping method, or a transfer method. Usually, the surface layer is formed on both sides, and the surface layer is hard and excellent in wiping property, and the back layer is selected for the purpose of scratching in handling and imparting post-workability, for example, imparting printability. The paint on the front and back sides is appropriately changed.

An acrylic type is a cross-linkable polymerizable compound having at least two (meth) acryloyloxy groups (meaning acryloyloxy group and / or methacryloyloxy group, hereinafter the same) in the molecule, and each (meth) acryloyloxy The residue to which the group is bonded is a hydrocarbon or a derivative thereof, and the molecule can contain an ether bond, a thioether bond, an ester bond, an amide bond, a urethane bond and the like.
Examples of silicon-based compositions include thermosetting polyorganosiloxane compositions appropriately blended with ultraviolet absorbers and the like. The polyorganosiloxane is a hydrolyzate and / or a partial condensate obtained by hydrolyzing and condensing a normal organosilane represented by the general formula R ¹ _n Si (OR ² ) _4-n. .

<Design layer and decorative film>
In this invention, it can also be set as the decorating film which provided the design layer in the single side | surface of the transparent resin film of this invention. As a method for forming a design layer, a desired design is printed directly on a film by gravure printing, flexographic printing, and the like, and is formed by heating and drying. It is formed by printing on a transfer sheet such as a biaxially stretched PET film. Examples include a method of transferring the design layer to the multilayer sheet by a method such as heat transfer. For example, printing is possible using polyester-based, polycarbonate-based, acrylic-based, or urethane-based printing inks, and surface treatment such as plasma, ion etching, corona discharge, etc., particularly when there is a problem with adhesion to the hard coat. It is also possible to improve the adhesion by improving the surface. Moreover, the method of providing a metal layer, a metal oxide layer, etc. on a film and using it as a design layer using a physical vapor deposition method or a chemical vapor deposition method is also mentioned.
The design layer may be directly laminated on the film, or may be laminated via a primer layer in order to improve adhesion with the film. The primer layer can be formed by applying a known primer agent on the film.

In the decorative film of the present invention, a thermoplastic resin film may be further laminated on the design layer in order to improve processability and design properties when the decorative molded body is used. The material of the thermoplastic resin film can be appropriately selected according to the material of the molded body in which the decorative film is integrated. Examples include polycarbonate resins, ABS resins, PVC resins, polystyrene resins such as impact polystyrene, polypropylene resins, acrylic resins, urethane resins, polyester resins, silicone resins, and mixtures of any two or more thereof.
The thermoplastic resin film may be laminated directly on the design layer or may be laminated via an adhesive layer.

<Three-dimensional molded body and in-mold molded body>
The three-dimensional molded article of the present invention is a molded article characterized by forming a design layer on one surface of the above-described film of the present invention and then subjecting it to pressure forming under heat and pressure, and having a pencil hardness of H or more. .
The in-mold molded body of the present invention is a molded body obtained by integrating the resin molded body and the decorative film of the present invention from the decorative film design surface side, and the thermoplastic resin film is added to the decorative film of the present invention. Is a molded body formed by integrating the resin molded body and the multilayer film from the thermoplastic resin film surface side.
The material of the molded body can be appropriately selected from known thermoplastic resins. For example, polycarbonate resins, ABS resins, PVC resins, polystyrene resins such as impact polystyrene, polypropylene resins, acrylic resins, urethane resins, polyester resins. Examples thereof include a resin, a silicone resin, and a mixture of any two or more thereof.
As a method of integrating the decorative film and the resin molded body, the decorative film is inserted into an injection mold without preforming, and a molten resin is injected there to form an injection molded body at the same time. A method of pasting a decorative film on a molded body, a decorative film is preformed by thermoforming (vacuum molding, pressure forming, vacuum pressure forming, etc.), then set in an injection mold, and molten resin there 3D surface decoration molding method that covers the surface of the molded body with a decorative film and integrates it, such as a method of forming an injection molded body and integrating it with a preformed decorative film at the same time Any method may be used.

Hereinafter, the present invention will be described specifically by way of examples. However, this invention is not restrict | limited at all by these Examples.
Evaluation of the films obtained in Examples and Comparative Examples was performed as follows.

<Weight average molecular weight>
A (meth) acrylate copolymer and a polycarbonate resin were similarly measured by GPC based on a calibration curve obtained by previously dissolving standard polystyrene in chloroform and measuring by gel permeation chromatography (GPC). The weight average molecular weight of each was calculated by comparing the two. The GPC device configuration is as follows.

Device: Weights 2690
Column: Shodex GPC KF-805L 8φ × 300 mm 2-linked developing solvent: chloroform flow rate: 1 ml / min
Temperature: 30 ° C
Detector: UV ... 486nm Polycarbonate RI ... Special acrylic

<Pencil hardness test>
In accordance with JIS K 5600-5-4, the hardness of the film was gradually increased to the surface of the film at an angle of 45 degrees and a load of 750 g with respect to the surface, and the pencil was pressed. evaluated. A pencil hardness of H or higher was accepted.

<Bending test>
A test piece having a flow direction of 50 mm × width direction of 30 mm was cut out from the center of the film, bent at 180 ° C. in the flow direction, and the presence or absence of breakage was confirmed. Those without breaking were considered acceptable.

<Thermoformability of the molded body>
The transparent multilayer sheets obtained in Examples and Comparative Examples were cut into 200 mm × 300 mm × each thickness, the obtained sample sheets were preheated to 150 ° C. with an infrared heater, and a mold ( Cushion type) was performed. The drawing height was 5 mm, and the evaluation was carried out.
Observe the surface condition (crack, wrinkle, unevenness, shape) of the molded product obtained at each temperature, shape the shape, and if no cracks, wrinkles, unevenness are observed, evaluate as “○” and crack When any one of wrinkles and unevenness was observed, it was evaluated as “×”.

Synthesis example 1
Synthesis of 2,2-bis (4-hydroxy-3-methylphenyl) propane / 2,2-bis (4-hydroxyphenyl) propane = 6/4 copolymer polycarbonate.
To 54.5 L of 9.0 w / w% sodium hydroxide aqueous solution, 6174.7 g (24.12 mol) of 2,2-bis (4-hydroxy-3-methylphenyl) propane (Honshu Chemical Co., Ltd.) and 2 , 2-bis (4-hydroxyphenyl) propane (manufactured by Nippon Steel Chemical Co., Ltd.) 4086 g (17.98 mol), triethylbenzylammonium chloride 3.8 g, and hydrosulfite 50.0 g were dissolved.
24 L of methylene chloride was added to this, and while maintaining the temperature at 15 ° C., 5390 g of phosgene was blown in over 40 minutes.
After completion of the phosgene blowing, 190 g of pt-butylphenol was added and stirred vigorously to emulsify the reaction solution. After emulsification, 110 ml of triethylamine was added, and the mixture was stirred at a temperature of 20 to 25 ° C. for about 1 hour for polymerization. It was.

  After completion of the polymerization, the reaction solution was separated into an aqueous phase and an organic phase, and the organic phase was neutralized with phosphoric acid. The organic phase was repeatedly washed with water until the conductivity of the washing water reached 10 μS / cm or less. The obtained organic phase was added dropwise to warm water maintained at 62 ° C., and the solvent was removed by evaporation to obtain a white powdery precipitate. The resulting precipitate was filtered and dried at a temperature of 120 ° C. for 24 hours to obtain the target polycarbonate polymer powder. The weight average molecular weight of the obtained polycarbonate was 33,000.

Example 1 [Production of Film (C1)]
As a (meth) acrylate copolymer, 40% by mass of Metabrene H-880 (manufactured by Mitsubishi Rayon Co., Ltd., weight average molecular weight: 14,000, a1 / a2 = 33/66) and 60% by mass of the polycarbonate of Synthesis Example 1 were charged. After mixing with a blender for 20 minutes, using a twin screw extruder with a screw diameter of 35 mm, the mixture was melt kneaded at a cylinder temperature of 260 ° C., extruded into a strand shape, and pelletized with a pelletizer.
Using a 40 mm single-screw extruder having a T die, the obtained pellets were melt extruded at a discharge rate of 40 kg / h and a cylinder temperature of 260 ° C., extruded into a film from the T die, and then a 120 ° C. mirror surface roll was used. It cooled and the film (C1) with a thickness of 180 micrometers was obtained.
The result of the pencil hardness test was 2H, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Example 2 [Production of Film (C2)]
Metablene H-880 25% by mass and 75% by mass of the polycarbonate of Synthesis Example 1 were mixed in a blender for 20 minutes, pelletized under the same conditions as in Example 1, and then molded under the same conditions as in Example 1. And a film (C2) having a thickness of 180 μm was obtained.
The result of the pencil hardness test was H, and the result of the bending test was no breakage. Further, the thermoformability was “◯” without any cracks, wrinkles or unevenness being observed.

Example 3 [Production of Film (C3)]
METABLEN H-880 40% by mass and 60% by mass of Iupilon E-2000 (Mitsubishi Engineering Plastics Co., Ltd., weight average molecular weight: 36,000) consisting of the structural unit of the above formula [3] as polycarbonate are charged with a blender and 20%. After being mixed for a while and pelletized under the same conditions as in Example 1, film formation was performed under the same conditions as in Example 1 to obtain a film (C3) having a thickness of 180 μm.
The result of the pencil hardness test was H, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Example 4 [Production of Hard Coat Film (C4)]
One side of the film obtained in Example 1 was coated with a UV-cured acrylic hard coat solution diluted with a solvent with a bar coater, dried, UV-irradiated, and cured to obtain a hard coat film. The result of the pencil hardness test was 3H, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Example 5 [Production of Hard Coat Film (C5)]
A UV cured acrylic hard coat solution diluted with a solvent was applied to one side of the film obtained in Example 3 with a bar coater, dried, UV irradiated, and cured to obtain a hard coat film. The result of the pencil hardness test was 2H, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Comparative Example 1 [Production of Film (D1)]
Using only the polycarbonate of Synthesis Example 1 as a material and pelletizing under the same conditions as in Example 1, film formation was performed under the same conditions as in Example 1 to obtain a film (D1) having a thickness of 180 μm.
The result of the pencil hardness test was F, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Comparative Example 2 [Production of Film (D2)]
Metablen H-880 10% by mass and Iupilon E-2000 90% by mass were mixed in a blender for 20 minutes, pelletized under the same conditions as in Example 1, and then molded under the same conditions as in Example 1. The film (D2) having a thickness of 180 μm was obtained.
The result of the pencil hardness test was B, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Comparative Example 3 [Production of Film (D3)]
The same conditions as in Example 1 except that only Iupilon E-2000 (Mitsubishi Engineering Plastics, weight average molecular weight: 36,000) was used as the material, the cylinder temperature was 280 ° C, and the mirror roll temperature was 130 ° C. Film forming was performed to obtain a film (D3) having a thickness of 180 μm.
The result of the pencil hardness test was 2B, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Comparative Example 4 [Production of Hard Coat Film (D4)]
A UV curable acrylic hard coat solution diluted with a solvent was applied to one side of the film obtained in Comparative Example 2 with a bar coater, dried, and then UV irradiated and cured to obtain a hard coat film. The result of the pencil hardness test was HB, and the result of the bending test was no breakage. The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Comparative Example 5 [Production of Hard Coat Film (D5)]
A UV-cured acrylic hard coat solution diluted with a solvent was applied to one side of the film obtained in Comparative Example 3 with a bar coater, dried, UV-irradiated, and cured to obtain a hard coat film. The result of the pencil hardness test was HB, and the result of the bending test was no breakage.
The thermoformability was “◯” with no cracks, wrinkles or unevenness observed.

Comparative Example 6 [Production of Film (D6)]
Using a multi-layer film forming machine having a single-screw extruder with a shaft diameter of 40 mm, a single-screw extruder with a shaft diameter of 75 mm, and a multi-manifold die connected to each extruder, a multi-layer film of polymethyl methacrylate and polycarbonate is formed. did. Polyethylene methacrylate ALTUGLAS V020 (manufactured by ARKEMA) was melt-extruded at a cylinder temperature of 240 ° C. and a discharge rate of 15 kg / h using a 40 mmΦ single-screw extruder, and polycarbonate Iupilon S-1000 (Mitsubishi) consisting of the structural unit of the above formula [3] Engineering Plastics, weight average molecular weight: 33,000) was melt extruded at a cylinder temperature of 270 ° C. and a discharge rate of 30 kg / h using a 75 mm single screw extruder. Both molten resins are laminated inside a multi-manifold die, extruded from a T-die as a film, cooled using a mirror roll at 110 ° C., and a multilayer film (D6) having an overall thickness of 180 μm and a polymethyl methacrylate layer thickness of 60 μm Got.
The result of the pencil hardness test on the polymethylmethacrylate surface was 2H, and the result of the bending test with the polymethylmethacrylate surface convex was broken. Moreover, wrinkles and unevenness were observed in the thermoformability and “x” was observed.

Comparative Example 7 [Production of Film (D7)]
Except for adjusting the discharge rate of Iupilon S-1000 to 52 kg / h and adjusting the rotation speed of the cooling roll, molding was performed under the same materials and conditions as in Comparative Example 6, and the total thickness was 180 μm and the polymethyl methacrylate layer thickness was 40 μm. A multilayer film (D7) was obtained.
The result of the pencil hardness test on the polymethyl methacrylate surface was H, and the result of the bending test with the polymethyl methacrylate surface being convex was broken. Moreover, wrinkles and unevenness were observed in the thermoformability and “x” was observed.

Comparative Example 8 [Production of Film (D8)]
60% by mass of Metablene H-880 and 40% by mass of Iupilon E-2000 were mixed in a blender for 20 minutes, pelletized under the same conditions as in Example 1, and then molded under the same conditions as in Example 1. And a film (D8) having a thickness of 180 μm was obtained.
The result of the pencil hardness test was 2H, and the result of the bending test was a break. In addition, cracks were observed in the thermoformability and “x” was obtained.

  From Tables 1-3, it turns out that the transparent resin film of this invention has high surface hardness, toughness, and flexibility.

  The transparent resin film of the present invention is characterized by having high flexibility and excellent surface hardness and thermoformability, and is suitably used for decorative film applications. The decorative molded body using the transparent resin film of the present invention is suitably used for housings of automobile interiors, home appliances, small portable machines and the like.

Claims (4)

(Meth) acrylate copolymer (A) 15 to 55% by mass containing 5 to 80% by mass of aromatic (meth) acrylate (a1) and 20 to 95% by mass of methyl methacrylate (a2), and the following formula [1]
([1] In the formula, R represents a single bond, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 10 carbon atoms, or a cyclic alkyl group having 3 to 8 carbon atoms, and X and Y are Each independently represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms) and a resin composition comprising 85 to 45% by mass of polycarbonate (B) containing a structural unit represented by a total thickness of 300 μm an der Ru off Irumu below,
The aromatic (meth) acrylate (a1) is phenyl (meth) acrylate or benzyl (meth) acrylate,
The polycarbonate (B) is represented by the following formula [2]
And the following formula [3]
The said film is a polycarbonate copolymer containing the structural unit of following, and the ratio of the structural unit of the said Formula [3] is 80 masses or less . The film according to claim 1 , wherein the film has a hard coat layer on one side and a pencil hardness of 2H or more. A three-dimensional molded article having a design layer on one surface of the film according to claim 1 or 2 and having a pencil hardness of H or more. Having a design layer on one surface of the film according to claim 1 or 2, in-mold molded article having a backing layer made of injection-molded article of the molten resin to said decorative layer side.