JP5428829B2 - Hard coat film for molding - Google Patents

Description

  The present invention relates to a hard coat film for molding which has good suppression of interference spots, excellent surface hardness and scratch resistance, and excellent moldability.

  Conventionally, as a film for molding, a polyvinyl chloride film has been representative, and due to recent needs for environmental resistance, unstretched films made of polyester, polycarbonate and acrylic resin, which have a low environmental load, and further heat resistance and resistance. A biaxially stretched polyester film having excellent solvent properties is used. (For example, see Patent Documents 1 to 10).

  For example, when a molding film is attached to a position where it touches the outside, such as a home appliance, a car nameplate or a building material member, in order to prevent scratches, the surface hardness of the molding film is supplemented and the scratch resistance is improved. A hard coat layer is provided on the surface.

  As a method for providing a hard coat layer on a molding film, a method is generally employed in which a hard coat layer is laminated after being molded by a pressure forming method, a vacuum forming method, or the like and then post-processed by a dipping method, a spray method or the like. However, in the above-described method, the hard coat layer is laminated by single-wafer processing, so that there is a limit to improvement in production speed and there is a problem in stability of quality. Therefore, after a hard coat layer is provided on a film before molding by a roll-to-roll method, a molded body by a method of molding is required.

  In the case of a method of laminating a hard coat layer before molding, as the characteristics required for the hard coat layer, surface hardness and scratch resistance comparable to the method of providing a hard coat layer in post-processing after molding are required, Formability that can follow the deformation accompanying molding is essential. However, in the case of a general hard coat resin, since the hard coat layer is too hard to satisfy the surface hardness, there is no moldability and cracks in the hard coat layer due to deformation during molding (cracking of the hard coat layer) There was a problem that occurred.

  Therefore, a hard coat film in which a flexible resin is laminated while having a certain degree of surface hardness after curing to improve moldability, and a layer having a flexible surface and a strong surface hardness on the substrate A hard coat film having strong surface hardness and flexibility has been proposed by laminating a plurality of layers (Patent Documents 11 to 14).

  In addition, in applications such as decorative materials, a higher level of quality has been demanded in recent years, and accordingly, a required level for suppressing iris-like colors (interference fringes) particularly under fluorescent lamps has increased. In addition, fluorescent lamps have become a three-wavelength type for daylight color reproducibility, and interference fringes are more likely to occur. Further, there is an increasing demand for cost reduction by simplifying the antireflection layer. Therefore, it is required to suppress interference fringes as much as possible with only the hard coat film (Patent Document 15).

Japanese Patent Laid-Open No. 9-156267 JP-A-9-187903 JP-A-10-296937 JP-A-11-268215 JP 2001-129951 A JP 2001-212868 A JP 2002-249652 A JP 2003-221606 A Japanese Patent Laid-Open No. 2004-075713 JP-A-2005-290354 JP 2005-305383 A JP 2007-284626 A JP 2007-313728 A International Publication No. 2008/029666 Pamphlet JP 2005-97571 A

  However, although the hard coat film proposed in Patent Documents 11 and 13 has an appropriate surface hardness, the hard coat film has only limited processing characteristics such as bendability and punching, and is proposed in Patent Document 12. Although the hard coat film has extensibility, the surface hardness was not satisfactory. In addition, although the hard coat film proposed in Patent Document 14 attempts to achieve both surface hardness and formability, it has sufficient performance in fields where higher formability and higher surface hardness are required. In some cases, it could not be demonstrated. That is, the above-mentioned patent document does not provide a hard coat film for molding that satisfies both high surface hardness and high moldability at the same time.

  The object of the present invention is to solve the above problems, that is, by processing and laminating a hard coat layer on a molding film before molding, it contributes to improving productivity and stability of quality. Another object of the present invention is to provide a hard coat film for molding which has both surface hardness, scratch resistance and moldability capable of following deformation at the time of molding, and has less interference spots.

  As a result of intensive studies to solve the above problems, the present inventors have finally completed the present invention. That is, the present invention is as follows.

1st invention is the hard-coat film for a shaping | molding laminated | stacked in order of the base film, the intermediate | middle layer, and the hard-coat layer, Comprising: A base film is a biaxially-oriented polyester film containing copolyester, The layer mainly comprises an aqueous polyester resin (A) and at least one of a water-soluble titanium chelate compound, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble zirconium acylate compound (B). As a constituent component, an aqueous coating solution containing a resin composition having a mixing ratio (mass ratio) of (A) / (B) of 10/90 to 95/5 is applied and dried. A coating liquid is applied and cured on the intermediate layer surface of the base film, and the coating liquid comprises an ionizing radiation curable compound having three or more functional groups, 1 and / or Or a bifunctional ionizing radiation curable compound, and the content of the mono- and / or bifunctional ionizing radiation curable compound in the ionizing radiation curable compound contained in the coating solution is 5% by mass or more and 95% by mass. % Ri der less, at least one ionizing radiation-curable compound contained in the coating liquid is a molding for a hard coat film is ionizing radiation-curable compound having an amino group.
2nd invention contains the particle | grains with an average particle diameter of 10 nm or more and 300 nm or less in the said hard-coat layer, The content in the hard-coat layer of the said particle | grain is 5 mass% or more and 70 mass% or less. It is a film.
In a third aspect of the invention, the hard coat layer contains an ionizing radiation curable silicone resin, and the content of the ionizing radiation curable silicone resin in the hard coat layer is 0 with respect to 100 parts by mass of the ionizing radiation curable compound. .. The hard coat film for molding that is 15 parts by mass or more and 15 parts by mass or less.
4th invention is the said copolyester resin in which the said water-based polyester resin (A) contains 1-10 mol% of aromatic dicarboxylic acid components containing a sulfonic-acid metal base with respect to all the dicarboxylic acid components of polyester. It is a hard coat film for molding.
5th invention is the said hard-coat film for shaping | molding whose glass transition temperature of the said water-based polyester resin (A) is 40 degreeC or more.
6th invention is a molded object formed by shape | molding the said hard-coat film for a shaping | molding.

  The hard coat film for molding according to the present invention has few iris colors under a fluorescent lamp, and has both characteristics of surface hardness, scratch resistance and moldability that can follow deformation during molding. Since the present invention has excellent visibility, high surface hardness, and excellent extensibility, it can be suitably used as, for example, a nameplate member or a building material member as a preferred embodiment. Further, as a preferred embodiment of the present invention, when an ionizing radiation curable resin or / and particles having an amino group are used, both characteristics of surface hardness and moldability can be achieved at a higher level. For example, as a member such as a housing It can be preferably used. Furthermore, the present invention does not require a hard coat process after molding, can contribute to productivity and stability of quality in the manufacturing process of the molding process, and is used as a film roll for molding as a preferred embodiment of the present invention. Is excellent in the quality stability of the molded body.

  Hereinafter, the present invention will be described in detail.

(Base film)
In the present invention, as the base film, a polyester film containing a copolymerized polyester excellent in moldability at the time of heat molding at a low temperature or low pressure is used. Here, moldability means that a molded body can be formed by a molding process such as mold molding, pressure molding, or vacuum molding. Specifically, it has a film stress characteristic that can form a molded body without breaking the base film even when a high stress is partially generated in a portion that is locally elongated by molding.

  Examples of the copolyester include (a) a copolyester composed of an aromatic dicarboxylic acid component, ethylene glycol, and a glycol component containing a branched aliphatic glycol or alicyclic glycol, or (b) terephthalic acid and isophthalic acid. A copolyester composed of an aromatic dicarboxylic acid component containing an acid and a glycol component containing ethylene glycol is preferred.

  When using a copolymer polyester composed of an aromatic dicarboxylic acid component, ethylene glycol, and a glycol component containing a branched aliphatic glycol or alicyclic glycol as the copolymer polyester, the aromatic dicarboxylic acid component is Terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid or ester-forming derivatives thereof are suitable, and the amount of terephthalic acid and / or naphthalenedicarboxylic acid component relative to the total dicarboxylic acid component is 70 mol% or more, preferably 85 mol% or more. Particularly preferred is 95 mol% or more, and particularly preferred is 100 mol%.

  In the present invention, the polyester film containing the copolymerized polyester includes a copolymerized polyester component as a component of the film, and specific examples thereof include the following. (1) The base film consists entirely of a copolymerized polyester, (2) the base film contains a copolymerized polyester as part of the constituent components (for example, a copolymerized polyester, polyethylene terephthalate, polyethylene naphthalate, etc. (Consisting of a resin composition mixed with another (homo) polyester), (3) a base film comprising a multilayer of a polyester layer containing a copolymerized polyester and a polyester layer not containing the copolymerized polyester.

  The base film is particularly preferably a biaxially stretched film from the viewpoints of heat resistance and solvent resistance. Examples of the stretching method include a tubular stretching method, a simultaneous biaxial stretching method, a sequential biaxial stretching method, and the like, but a sequential biaxial stretching method is preferable in view of flatness, dimensional stability, thickness unevenness, and the like. For example, as a sequential biaxial stretching method in the case of using a polyester film as a base film, the film is stretched in the longitudinal direction from 50 ° C. to 110 ° C. in the longitudinal direction and from 1.6 times to 4.0 times in the longitudinal direction. After preheating, it can be stretched in the width direction from 1.2 times to 5.0 times at a glass transition temperature of -40 ° C to + 65 ° C. Furthermore, after the biaxial stretching, a heat setting treatment can be performed at a temperature of −40 ° C. or more and −10 ° C. or less of the melting point of the polyester.

  In order for the base film used by this invention to provide handling property (for example, winding property after lamination | stacking), it is preferable to make a film contain particle | grains and to form a processus | protrusion on the film surface. As particles to be included in the film, inorganic particles such as silica, kaolinite, talc, calcium carbonate, zeolite, alumina, etc., heat resistant polymer particles such as acrylic, PMMA, nylon, polystyrene, polyester, benzoguanamine / formalin condensate, etc. Is mentioned. From the viewpoint of transparency, the content of particles in the film is preferably small, for example, preferably 1 ppm or more and 1000 ppm or less. Furthermore, it is preferable to select particles having a refractive index close to that of the resin used from the viewpoint of transparency. Moreover, in order to provide various functions as needed, the film may contain a light-resistant agent (ultraviolet ray inhibitor), a pigment, an antistatic agent, and the like.

  When the hard coat film for molding is printed, for example, on the surface where the hard coat layer is not laminated, it is preferable that the total light transmittance of the base film is 80% or more and the haze is 5% or less. When the transparency of the substrate film is inferior, the visibility when the printed layer is viewed from the hard coat layer side is lowered.

  The base film used in the present invention may be a single layer film or a composite film having two or more layers in which a surface layer and a center layer are laminated. In the case of a composite film, there is an advantage that the functions of the surface layer and the center layer can be designed independently. For example, by containing particles only on the thin surface layer and forming irregularities on the surface, the handling property is maintained, but the thick central layer does not substantially contain particles, so that the composite film as a whole is transparent. Can be further improved. The method for producing the composite film is not particularly limited, but considering productivity, after extruding the raw material of the surface layer and the central layer from separate extruders, leading to one die and obtaining an unstretched sheet, Lamination by a so-called coextrusion method that is oriented in at least one axial direction is preferable.

  The lower limit of the thickness of the substrate film used in the present invention is preferably 35 μm or more, more preferably 50 μm or more. On the other hand, the upper limit of the thickness is preferably 260 μm or less, more preferably 200 μm or less. When the thickness is small, not only the handling property becomes poor, but also when heated at the time of drying so as to reduce the residual solvent of the hard coat layer, the film tends to be wrinkled and flatness tends to be poor. On the other hand, when the thickness is large, not only is there a problem in terms of cost, but flatness due to curling tends to occur when the material is wound and stored in a roll shape.

(Middle layer)
In the hard coat film for molding of the present invention, the intermediate layer has an aqueous polyester resin (A) and a water-soluble titanium chelate compound, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble zirconium acylate. It consists of a resin composition in which at least one compound (B) is a main constituent and the mixing ratio (mass ratio) of (A) / (B) is 10/90 to 95/5.

  In the present invention, by using the intermediate layer, a resin constituting the intermediate layer so that the refractive index difference between the polyester film of the base material and the intermediate layer and the refractive index difference between the intermediate layer and the hard coat layer are reduced. The refractive index of the intermediate layer can be controlled by the type and content of the additive, while maintaining the adhesion with the hard coat layer and the adhesion under high temperature and high humidity (humidity heat resistance) The iris color can be suppressed.

  This resin composition is heated with heat during the stretching process of the base film, so that at least one of a titanium chelate compound, a titanium acylate compound, a zirconium chelate compound, or a zirconium acylate compound (B) is a polyester resin. A uniform film is formed by the crosslinking reaction. That is, since the metal chelate compound or metal acylate compound is decomposed by heat treatment, it does not exist in the intermediate layer in a state of being added to the aqueous coating solution.

Therefore, the content of the metal chelate compound or metal acylate compound in the aqueous coating solution is calculated from the content of the metal element (Ti or Zr) in the intermediate layer after the heat treatment as follows.
(1) First, the type of chelate or acylate contained in the aqueous coating solution is identified from the chelate or acylate residue in the intermediate layer.
(2) Next, the content of the metal chelate compound or metal acylate compound in the aqueous coating solution is calculated from the content of the metal element (Ti or Zr) in the intermediate layer.

  The refractive index of the intermediate layer is higher than that of the polyester resin (A) alone by increasing the composition ratio of at least one of the titanium chelate compound, titanium acylate compound, zirconium chelate compound, or zirconium acylate compound (B). Can also be high.

  In the polyester resin (A) used in the present invention, an active site such as a hydroxyl group or a carboxyl group may be introduced into the molecular chain. A cross-linking reaction takes place in this place, resulting in a dense film.

  Moreover, in order to give the same crosslinkability with an acrylic resin, it is necessary to introduce a crosslinkable functional group. However, since the refractive index of the acrylic resin itself is low, even when a titanium chelate compound, a titanium acylate compound, a zirconium chelate compound, or a zirconium acylate compound is used in combination, the refractive index is controlled to be the same as that of the intermediate layer of the present invention. It is difficult.

  Furthermore, since the polyester resin (A), which is a constituent component of the intermediate layer, is involved in adhesion to the base polyester film, the composition ratio (A / B) of the aqueous polyester resin (A) and the compound (B) is When the ratio is less than 10/90, the adhesion to the base film is lowered, and the stretchability as an intermediate layer is lowered, and it is not uniform during stretching. Therefore, the transparency required for optical use decreases, and the adhesion with the hard coat layer formed on the easy-adhesion layer becomes a problem. On the other hand, when the composition ratio (A / B) between the aqueous polyester resin (A) and the compound (B) exceeds 95/5, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble Crosslinking by the zirconium acylate compound (B) becomes poor, and the refractive index also decreases. For this reason, the adhesion (humidity and heat resistance) under high temperature and high humidity is lowered, and the effect of suppressing iris-like colors under a fluorescent lamp is insufficient.

  The aqueous polyester resin (A) of the present invention is dissolved or dispersed in water or a water-soluble organic solvent (for example, an aqueous solution containing less than 50% by mass of alcohol, alkyl cellosolve, ketone, or ether). Means a polyester resin capable of In order to impart water resistance to the polyester resin, it is important to introduce a hydrophilic group such as a hydroxyl group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, or an ether group into the molecular chain of the polyester resin. Among the hydrophilic groups, sulfonic acid groups are preferable from the viewpoint of coating film properties and adhesion.

  When the sulfonic acid group is introduced into the polyester, the sulfonic acid compound is more preferably 1 to 10 mol% in the total acid component of the polyester. When the amount of the sulfonic acid group is less than 1 mol%, the polyester resin does not exhibit water, and a water-soluble titanium chelate compound, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble zirconium acylate compound Since the compatibility with at least one of (B) also decreases, it becomes difficult to obtain a uniform and transparent intermediate layer. Moreover, when the amount of sulfonic acid group exceeds 10 mol%, it becomes easy to be inferior to the adhesiveness (humidity heat resistance) under high temperature and high humidity.

  Further, the aqueous polyester resin (A) preferably has a glass transition temperature of 40 ° C. or higher. For this reason, the acid component of the polyester resin (A) is preferably composed mainly of an aromatic group such as terephthalic acid, isophthalic acid, or naphthalenedicarboxylic acid. The glycol component is preferably a glycol having a relatively small carbon number such as ethylene glycol, propane glycol, 1,4-butanediol, or neopentyl glycol, or an aromatic system such as an ethylene oxide adduct of bisphenol A. Further, as a raw material of the polyester resin (A), a rigid component such as biphenyl or a dicarboxylic acid component or diol component having a high refractive index atom such as bromine or sulfur may be used within a range in which the physical properties of the film do not deteriorate. Good. When the glass transition temperature of the polyester resin (A) is less than 40 ° C., the adhesiveness (humidity heat resistance) under high temperature and high humidity tends to be insufficient. Furthermore, since the refractive index of the polyester resin (A) also decreases, the refractive index of the intermediate layer also decreases. As a result, the suppression of iris color under fluorescent lamps tends to be insufficient.

  The other main component of the intermediate layer is at least one (B) of a water-soluble titanium chelate compound, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble zirconium acylate compound. The above water-soluble means to dissolve in water or an aqueous solution containing less than 50% by mass of a water-soluble organic solvent.

  Examples of water-soluble titanium chelate compounds include diisopropoxybis (acetylacetonato) titanium, isopropoxy (2-ethyl-1,3-hexanediolato) titanium, diisopropoxybis (triethanolaminato) titanium, di -N-butoxybis (triethanolaminato) titanium, hydroxybis (lactato) titanium, ammonium salt of hydroxybis (lactato) titanium, titanium beloxocitrate ammonium salt and the like.

  Examples of the water-soluble titanium acylate compound include oxotitanium bis (monoammonium oxalate), and examples of the water-soluble zirconium compound include zirconium tetraacetylacetonate and zirconium acetate.

  In the intermediate layer, a resin other than the main component, for example, an acrylic resin, a polyurethane resin, a polyester resin, an alkyd resin, a vinyl resin such as polyvinyl alcohol, or the like is used in a range that does not affect the effects of the present invention. It doesn't matter. Further, the combined use of the crosslinking agent is not particularly limited as long as the effect of the present invention is not affected. Examples of crosslinking agents that can be used include adducts of urea, melamine, benzoguanamine, and the like with formaldehyde, amino resins such as alkyl ether compounds composed of these adducts and alcohols having 1 to 6 carbon atoms, polyfunctional epoxy compounds, Examples thereof include a polyfunctional isocyanate compound, a blocked isocyanate compound, a polyfunctional aziridine compound, and an oxazoline compound.

  In the present invention, the aqueous coating solution used for forming the intermediate layer includes an aqueous polyester resin (A), a water-soluble titanium chelate compound, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble An aqueous coating solution mainly composed of at least one (B) zirconium acylate compound and an aqueous solvent. When applying the aqueous coating solution to the surface of the polyester film, an appropriate amount of a known anionic surfactant or nonionic surfactant is used in order to improve the wettability to the film and coat the aqueous coating solution uniformly. It is preferable to add.

  In addition, in the aqueous coating solution, inorganic and / or heat-resistant polymer particles, antistatic agents, ultraviolet absorbers, etc. in order to impart other functions such as handling properties, antistatic properties and antibacterial properties to the film. Additives such as organic lubricants, antibacterial agents, and photo-oxidation catalysts can be included.

  As the solvent used in the aqueous coating solution, in addition to water, alcohols such as ethanol, isopropyl alcohol, and benzyl alcohol may be mixed in a range of less than 50% by mass with respect to the total aqueous coating solution. Furthermore, if it is less than 10 mass%, you may mix in the range which can melt | dissolve organic solvents other than alcohol. However, the total amount of alcohols and other organic solvents in the aqueous coating solution is preferably less than 50% by mass.

(Hard coat layer)
In the hard coat film for molding of the present invention, a hard coat layer is laminated on at least one surface of a base film via an intermediate layer. In the present invention, the hard coat layer has a coating with a hardness higher than that of the base material in order to supplement the surface hardness of the base material made of the base film and improve the scratch resistance, and also to deformation during molding. The layer which has the outstanding moldability which can be followed is shown. More specifically, the hard coat film for molding of the present invention has a pencil hardness of at least H as the surface hardness, and an elongation of at least 10% according to the evaluation method described below. It can be suitably used as a member for use or for building materials.

  The hard coat layer that can be used in the present invention needs to contain an ionizing radiation curable resin as a main component. Unlike the thermosetting resin, heat treatment at the time of curing is not required, and heat shrinkage of the base film due to heat can be reduced, which is preferable. In the present invention, the ionizing radiation curable compound refers to a compound that polymerizes and / or reacts when irradiated with an electron beam, radiation, or ultraviolet light, and the compound reacts and / or reacts. A hard coat layer is formed. Examples of the ionizing radiation curable compound used in the present invention include melamine-based, acrylic and silicon-based ionizing radiation curable compounds. Among them, acrylate-based ionizing radiation curable compounds are preferable in terms of obtaining high surface hardness. .

  In the present invention, the ionizing radiation curable compound includes not only monomers and precursors but also ionizing radiation curable resins obtained by polymerization and / or reaction thereof. For example, examples of the acrylate ionizing radiation curable compound include polyurethane acrylate, polyester acrylate, epoxy acrylate, polyol acrylate and the like, but are not particularly limited, and any acrylate ionizing radiation curable compound may be used. .

  The hard coat layer in the present invention is applied to a base film with a coating solution containing at least an ionizing radiation curable compound having three or more functional groups and a monofunctional and / or bifunctional ionizing radiation curable compound, and then an electron beam. It is cured by polymerizing and / or reacting by irradiation with either radiation or ultraviolet rays.

  When an acrylate ionizing radiation curable compound is used as the ionizing radiation curable compound, the monofunctional (monofunctional) acrylate ionizing radiation curable compound in the present invention has at least one (meth) acryloyl group in the molecule. If it is a compound to contain, it will not restrict | limit in particular. For example, acrylamide, (meth) acryloylmorpholine, 7-amino-3,7-dimethyloctyl (meth) acrylate, isobutoxymethyl (meth) acrylamide, isobornyloxyethyl (meth) acrylate, isobornyl (meth) acrylate, 2 -Ethylhexyl (meth) acrylate, ethyl diethylene glycol (meth) acrylate, t-octyl (meth) acrylamide, diacetone (meth) acrylamide, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, lauryl (meth) acrylate, di Cyclopentadiene (meth) acrylate, dicyclopentenyloxyethyl (meth) acrylate, dicyclopentenyl (meth) acrylate, N, N-dimethyl (meth) Kurylamide tetrachlorophenyl (meth) acrylate, 2-tetrachlorophenoxyethyl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, tetrabromophenyl (meth) acrylate, 2-tetrabromophenoxyethyl (meth) acrylate, 2-trichloro Phenoxyethyl (meth) acrylate, tribromophenyl (meth) acrylate, 2-tribromophenoxyethyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, vinyl caprolactam, N-vinyl Pyrrolidone, N-vinylformamide, phenoxyethyl (meth) acrylate, butoxyethyl (meth) acrylate, pentachlorophenyl (meth) acrylate, Tabromophenyl (meth) acrylate, polyethylene glycol mono (meth) acrylate, polypropylene glycol mono (meth) acrylate, bornyl (meth) acrylate, methyltriethylene diglycol (meth) acrylate, cyclohexyl (meth) acrylate, nonylphenyl (meth) ) Derivatives such as acrylate and its modified caprolactone, acrylic acid and the like, and mixtures thereof.

  When an acrylate ionizing radiation curable compound is used as the ionizing radiation curable compound, the bifunctional acrylate ionizing radiation curable compound in the present invention is a polyhydric alcohol having two or more alcoholic hydroxyl groups in one molecule. A compound in which the hydroxyl group is an esterified product of two (meth) acrylic acids can be used. Specifically, (a) C2-C12 alkylene glycol (meth) acrylic acid diesters: ethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, 1,4-butanediol di (meth) ) Acrylate, neopentyl glycol di (meth) acrylate, 1,6-hexanediol (meth) acrylate, etc. (b) (meth) acrylate diesters of polyoxyalkylene glycol: diethylene glycol di (meth) acrylate, triethylene glycol Di (meth) acrylate, tetraethylene glycol di (meth) acrylate, dipropylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate (C) (meth) acrylic acid diesters of polyhydric alcohols: (e) pentaerythritol di (meth) acrylate, etc. (d) bisphenol A or bisphenol A hydride ethylene oxide and propylene oxide adduct (meth) acrylic acid diester Class: 2,2′-bis (4-acryloxyethoxyphenyl) propane, 2,2′-bis (4-acryloxypropoxyphenyl) propane, etc. (e) a polyvalent isocyanate compound and two or more alcoholic hydroxyl groups Urethane (meth) acrylate having two (meth) acryloyloxy groups in the molecule obtained by further reacting an alcoholic hydroxyl group-containing (meth) acrylate with a terminal isocyanate group-containing compound obtained by reacting the containing compound in advance (F) two or more epoxies in the molecule Epoxy (meth) acrylates having two (meth) acryloyloxy groups in the resulting molecule to a compound having a sheet group by reacting acrylic acid or methacrylic acid, and the like.

  When an acrylate ionizing radiation curable compound is used as the ionizing radiation curable compound, the trifunctional or higher functional acrylate ionizing radiation curable compound in the present invention includes (a) specifically pentaerythritol tri (meth) acrylate, Pentaerythritol tetra (meth) acrylate, dipentaerythritol tri (meth) acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, trimethylolpropane tri (meta) ) Such as acrylate, (b) a terminal isocyanate group-containing compound obtained by previously reacting a polyvalent isocyanate compound with two or more alcoholic hydroxyl group-containing compounds, and further containing an alcoholic hydroxyl group Urethane (meth) acrylates having 3 or more (meth) acryloyloxy groups in the molecule obtained by reacting (meth) acrylate, (c) Acrylic acid or a compound having 3 or more epoxy groups in the molecule Examples thereof include epoxy (meth) acrylates having 3 or more (meth) acryloyloxy groups in the molecule obtained by reacting methacrylic acid.

  In the present invention, the ionizing radiation curable compound contained in the coating solution contains one or more ionizing radiation curable compounds having three or more functional groups in addition to the one or bifunctional ionizing radiation curable compound. is important. In the hard coat layer after curing, a tri- or higher functional ionizing radiation curable compound component having a high crosslinking density is used as a hard segment, and the mono- and / or bi-functional ionizing radiation curable compound reacts to form a hard segment, and 1 and A bifunctional ionizing radiation curable compound component is present as a soft segment. Thus, by adjusting two or more types of ionizing radiation curable compounds having different functional numbers within a specific concentration range, a hetero-crosslinked structure is introduced into the hard coat layer, and the surface hardness and scratch resistance are improved by the hard segment. It was possible to obtain a remarkable effect of providing both the contradictory properties of imparting and imparting moldability by the stretchability of the soft segment.

  In the present invention, in order to achieve both high surface hardness and excellent moldability, specifically, pencil hardness of H or higher and elongation of 10% or higher, 1 in the ionizing radiation curable compound contained in the coating solution. It is important that the content of the bifunctional ionizing radiation curable compound is 5% by mass or more and 95% by mass or less. When the content is less than 5% by mass, not only the flexibility of the coating is lowered, but also cracks are generated in the hard coat layer during molding, which is not preferable. Moreover, when the said content exceeds 95 mass%, it is difficult to obtain the cured film which has sufficient surface hardness and abrasion resistance. The lower limit of the content is more preferably 10% by mass or more, and further preferably 20% by mass or more. Moreover, 90 mass% or less is more preferable, as for the upper limit of the said content, 80 mass% or less is more preferable, and 70 mass% or less is more preferable. . When the content of the monofunctional and / or bifunctional ionizing radiation curable compound in the ionizing radiation curable compound is 20% by mass or more and 80% by mass or less, both the surface height and the moldability are more highly balanced. Specifically, pencil hardness of 2H or more and elongation of 20% or more can be achieved at the same time, and high hardness and high workability are required at the same time, for example, for nameplates such as automobiles and casings for portable devices. It is suitable for a molding film.

  Furthermore, the present inventor has found that, in addition to the above-described embodiment, by using an ionizing radiation curable compound having an amino group as the ionizing radiation curable compound, both surface hardness and moldability can be achieved to a higher degree. That is, it is preferable that at least one ionizing radiation curable compound contained in the coating solution has an amino group. About the said effect | action by using the compound which has an amino group as an ionizing radiation hardening compound, it thinks as follows. When the hard coat layer has a partial hardness distribution difference, local cracking is likely to occur when the hard coat layer is stretched. As a factor of such a difference in the partial hardness distribution, there is polymerization inhibition (oxygen inhibition) of the ionizing radiation curable resin by oxygen. Here, when a compound having an amino group is used as the ionizing radiation curing compound, the amino group traps radical oxygen, and the influence of oxygen inhibition on the curing reaction of the surface layer portion of the hard coat layer is reduced. A uniform curing reaction proceeds. As a result, the stress applied to the hard coat layer during molding is dispersed throughout the layer, and the occurrence of cracks during molding is suppressed. Therefore, it is considered that the surface height and moldability can be achieved at a higher level. In addition to the above effects, the surface of the hard coat layer is hardened more than when no amino group is contained due to the effect of fast curing of the coating film due to the inclusion of amino groups as the ionizing radiation curable resin. Hardness can be improved.

  The content of the ionizing radiation curable compound containing an amino group in the ionizing radiation curable compound contained in the coating solution is preferably 2.5% by mass or more and 95% by mass or less. The lower limit of the content of the ionizing radiation curable compound containing an amino group in the ionizing radiation curable compound contained in the coating solution is more preferably 5% by mass or more, and further preferably 10% by mass or more. . The upper limit of the content is more preferably 92.5% by mass or less, further preferably 90% by mass or less, and further preferably 50% by mass or less. When the content of the ionizing radiation curable compound containing an amino group in the ionizing radiation curable compound contained in the coating solution is less than 2.5% by mass, it is difficult to uniformly cure the entire hard coat layer. It becomes difficult to obtain resistance to cracks. Further, when the ionizing radiation curable compound containing an amino group becomes high in concentration, yellowing of the hard coat layer becomes strong due to the amino group. Therefore, when the content exceeds 95% by mass, high transparency is impaired. May be. For example, when printing is performed on the surface on which the hard coat layer is not laminated, the color b value of the film is preferably 2 or less. In this case, the ionizing radiation curable compound containing the amino group is 92.5% by mass or less. It is preferable that

  In the present invention, the coating solution contains a monofunctional and / or bifunctional ionizing radiation curable compound and an ionizing radiation curable compound having three or more functional groups. The ionizing radiation curable compound of the part may be any one containing an amino group. Further, any one of a monofunctional ionizing radiation curable compound, a bifunctional ionizing radiation curable compound, or an ionizing radiation curable compound having three or more functional groups is an ionizing radiation curable compound containing an amino group. Is also a preferred embodiment.

  When an acrylate ionizing radiation curable compound is used as the ionizing radiation curable compound having an amino group, examples of the acrylate ionizing radiation curable compound having an amino group include acrylamide, 7-amino-3,7-dimethyloctyl ( (Meth) acrylate, isobutoxymethyl (meth) acrylamide, t-octyl (meth) acrylamide, diacetone (meth) acrylamide, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, N, N-dimethyl (meth) acrylamide Examples include tetrachlorophenyl (meth) acrylate and N-vinylformamide.

  In addition to the above embodiment, the inventor of the present application has found that by including particles in the hard coat layer, the moldability can be further improved, and the surface hardness and the moldability can be enhanced at a high level. About the effect | action which a moldability improves more by containing particle | grains in a hard-coat layer, it thinks as follows. When the hardness of the hard coat layer is increased, a strong stress is temporarily generated in the hard coat layer having high hardness at the time of molding, so that the hard coat layer is cracked at once. Here, the presence of particles in the hard coat layer relieves internal stress applied to the hard coat layer at the time of molding at the interface between the ionizing radiation curable compound and the particles and suppresses the generation of cracks. It is thought that there is an effect that micro cracks that cannot be confirmed by visual inspection to the extent that it does not impair the appearance are generated in advance, the occurrence of fatal cracks in the hard coat layer is delayed, and as a result, the effect of improving moldability appears It is done.

  Examples of the particles included in the hard coat layer include amorphous silica, crystalline silica, silica-alumina composite oxide, kaolinite, talc, calcium carbonate (calcite type, vaterite type), zeolite, alumina, hydroxyapatite, and the like. Heat-resistant polymer particles such as inorganic particles, crosslinked acrylic particles, crosslinked PMMA particles, crosslinked polystyrene particles, nylon particles, polyester particles, benzoguanamine / formalin condensate particles, benzoguanamine / melamine / formaldehyde condensate particles, melamine / formaldehyde condensate particles, Organic / inorganic hybrid fine particles such as silica / acrylic composite compounds may be mentioned, but in the present invention, the type of particles is not particularly limited.

  Examples of the shape of the particles include a spherical shape, a block shape, a plate shape, a fiber shape, and a flake shape. However, the shape of the particles is not particularly limited. In view of the above, spherical particles are preferable.

  In the present invention, the average particle diameter of the particles is preferably 10 nm or more and 300 nm or less, the lower limit is preferably 40 nm or more, and the upper limit is preferably 200 nm or less, particularly the lower limit is 50 nm or more and the upper limit is 100 nm or less. preferable. When the average particle diameter of the particles is smaller than 10 nm, the average particle diameter is too small, and therefore, any or all of the effects of improving the surface hardness, scratch resistance, and moldability described above may be small. Moreover, when it exceeds 300 nm, a hard-coat layer becomes weak and a moldability may fall. The average particle diameter is an average particle diameter measured by dispersing the particles in a solvent that does not swell using a Coulter counter (manufactured by Beckman Coulter, Multisizer II type).

  In the present invention, the content of the particles to be contained in the hard coat layer is preferably 5% by mass or more and 70% by mass or less as a solid component in the hard coat layer, and particularly preferably, the lower limit of the content is 15% by mass. The upper limit is 50% by mass or less. When the content of the particles is less than 5% by mass, any of the above-described effects of improving the surface hardness, scratch resistance, and moldability due to the addition of the particles may be reduced. On the other hand, when the content of the particles exceeds 70% by mass, a large amount of the fine cracks described above are generated at the time of molding, and haze increases (whitens), thereby impairing the transparency of the molded body.

  Furthermore, in addition to the above embodiment, the inventor of the present application contains an ionizing radiation curable silicone resin in the hard coat layer, thereby imparting slipperiness, improving the scratch resistance of the surface, and further increasing the surface hardness and moldability. I found that they can be compatible. Further, according to such an embodiment, the ionizing radiation curable silicone resin itself is cross-linked by the curing reaction, and in some cases, the ionizing radiation curable resin constituting the hard coat layer is also cross-linked. When using a molded body formed by molding the hard coat film for molding of the present invention for a long period of time, it is possible to obtain a new effect that the function of the surface scratch resistance over time is not impaired. it can.

  The ionizing radiation curable silicone resin is, for example, a radical addition type having an alkenyl group and a mercapto group, a hydrosilylation reaction type having an alkenyl group and a hydrogen atom, a cationic polymerization type having an epoxy group, and a (meth) acryl group. A radical polymerization type silicone resin having Among these, a cationic polymerization type having an epoxy group and a radical polymerization type having a (meth) acryl group are preferable.

  Examples of silicone resins having an epoxy group or (meth) acryl group in the molecule include epoxypropoxypropyl-terminated polydimethylsiloxane, (epoxycyclohexylethyl) methylsiloxane-dimethylsiloxane copolymer, methacryloxypropyl-terminated polydimethylsiloxane, and acryloxy. And propyl-terminated polydimethylsiloxane. Examples of the silicone resin having a vinyl group in the molecule include terminal vinyl polydimethylsiloxane and vinylmethylsiloxane homopolymer.

  In the present invention, the addition amount of the ionizing radiation curable silicone resin to be contained in the hard coat layer is preferably 0.15 to 15 parts by mass with respect to 100 parts by mass of the ionizing radiation curable compound for constituting the hard coat layer. More preferably, 0.3 to 13 parts by mass, and still more preferably 0.5 to 5 parts by mass are blended. When the blending amount of the ionizing radiation curable silicone resin is less than the lower limit, the effect of improving the scratch resistance when formed into a molded product is poor, and when it exceeds the upper limit, the hard coat layer is sufficiently cured when formed. It may not be possible. The ionizing radiation curable silicone resin contained in the hard coat layer may be used alone or in combination of two or more.

  In the present invention, it is desirable to appropriately select or combine the use of a compound having an amino group as the ionizing radiation curable compound and the addition of particles to the hard coat layer according to the use of the film for molding as described above. . A particularly preferred embodiment is a combination thereof. As a result, the surface hardness and moldability of the hard coat layer can be made extremely highly compatible. Specifically, the surface hardness is 2H or higher and the elongation is 20% or higher, more preferably the surface hardness is 2H or higher. In addition, a molding hard coat film having an elongation of 30% or more can be obtained, and for example, it can be suitably used for applications such as a cover member for automobiles, a deep housing or container.

  In the present invention, as a method of polymerizing and / or reacting the coating solution, a method of irradiating with an electron beam, radiation, or ultraviolet rays may be mentioned. When ultraviolet rays are irradiated, a photopolymerization initiator is added to the coating solution. Is desirable.

  Specific examples of the photopolymerization initiator include acetophenone, 2,2-diethoxyacetophenone, p-dimethylacetophenone, p-dimethylaminopropiophenone, benzophenone, 2-chlorobenzophenone, 4,4′-dichlorobenzophenone, 4,4′-bisdiethylaminobenzophenone, Michler's ketone, benzyl, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, methylbenzoyl formate, p-isopropyl-α-hydroxyisobutylphenone, α-hydroxyisobutylphenone, 2, Carbonyl compounds such as 2-dimethoxy-2-phenylacetophenone and 1-hydroxycyclohexyl phenyl ketone, tetramethylthiuram monosulfide, tetramethylthiuramdis Examples thereof include sulfur compounds such as rufide, thioxanthone, 2-chlorothioxanthone, and 2-methylthioxanthone, and peroxide compounds such as benzoyl peroxide and di-t-butyl peroxide. Examples of these photopolymerization-initiated peroxide compounds such as t-butyl peroxide. These photopolymerization initiators may be used alone or in combination of two or more. The addition amount of the photopolymerization initiator is suitably 0.01 parts by weight or more and 15 parts by weight or less per 100 parts by weight of the ionizing radiation curable compound contained in the coating solution, and the reaction is slow when the amount used is small. In addition to the poor quality, the remaining unreacted material does not provide sufficient surface hardness and scratch resistance. On the other hand, when the addition amount is large, there is a problem that the hard coat layer is yellowed by the photopolymerization initiator.

  In the present invention, the coating solution contains a known thermal polymerization inhibitor such as hydroquinone, hydroquinone monomethyl ether, 2,5-t-butyl hydroquinone, etc. in order to prevent thermal polymerization during production and dark reaction during storage. It is preferable to add. The addition amount of the thermal polymerization inhibitor is preferably 0.005 parts by mass or more and 0.05 parts by mass or less per 100 parts by mass of the ionizing radiation curable compound contained in the coating solution.

  In the present invention, an organic solvent can be blended in the coating solution for the purpose of improving workability during coating and controlling the coating film thickness as long as the object of the present invention is not impaired.

  As the organic solvent, when a base film having a low melting point is used, it may be necessary to adjust the drying temperature after coating to 150 ° C. or lower, so the boiling point of the organic solvent is 50 ° C. or higher and 150 ° C. or lower. Is preferred. Specific examples include alcohol solvents such as methanol, ethanol and isopropyl alcohol, acetate solvents such as methyl acetate, ethyl acetate and butyl acetate, ketone solvents such as acetone and methyl ethyl ketone, and aromatic solvents such as toluene. And cyclic ether solvents such as dioxane. These solvents can be used alone or in admixture of two or more.

  In the present invention, the coating liquid should have a surface tension lowered to improve the coating appearance of the hard coat layer, in particular, dents due to fine bubbles, dents due to adhesion of foreign matters, and repellency in the drying process. For the purpose, a surfactant can be contained.

  As the surfactant, known cationic, anionic, and nonionic surfactants can be suitably used, but they have polar groups due to problems such as alteration of the coating solution and poor adhesion of the hard coat layer to the base film. The nonionic type | system | group which is not carried out is preferable, and also the silicone type surfactant or fluorine-type surfactant which is excellent in surface active ability is preferable.

  Silicone surfactants include dimethyl silicon, amino silane, acrylic silane, vinyl benzyl silane, vinyl benzyl silyl amino silane, glycid silane, mercapto silane, dimethyl silane, polydimethyl siloxane, polyalkoxy siloxane, hydrodiene modified siloxane, vinyl modified siloxane, Vitroxy modified siloxane, amino modified siloxane, carboxyl modified siloxane, halogenated modified siloxane, epoxy modified siloxane, methacryloxy modified siloxane, mercapto modified siloxane, fluorine modified siloxane, alkyl group modified siloxane, phenyl modified siloxane, alkylene oxide modified siloxane, etc. .

  Fluorosurfactants include ethylene tetrafluoride, perfluoroalkyl ammonium salt, perfluoroalkyl sulfonic acid amide, sodium perfluoroalkyl sulfonate, perfluoroalkyl potassium salt, perfluoroalkyl carboxylate, perfluoroalkyl sulfone. Acid salts, perfluoroalkyl ethylene oxide adducts, perfluoroalkyl trimethyl ammonium salts, perfluoroalkyl amino sulfonates, perfluoroalkyl phosphate esters, perfluoroalkyl alkyl compounds, perfluoroalkyl alkyl betaines, perfluoroalkyl halides, etc. Is mentioned.

  From the viewpoint of improvement in coating appearance and slipperiness, the content of the surfactant is preferably 0.01% by mass or more with respect to the coating liquid constituting the hard coat layer. On the other hand, since the surfactant bleeds out to the surface of the hard coat layer and contaminates what touched the hard coat layer, the surfactant content is preferably 2.00% by mass or less.

  The surfactant used preferably has an HLB of 2 or more and 12 or less. By using a surfactant having an HLB of 2 or more, the leveling property due to the surface activity can be improved. The HLB of the surfactant is more preferably 3 or more, and particularly preferably 4 or more. On the other hand, by using a surfactant having an HLB of 12 or less, deterioration of slipperiness can be suppressed.

  Note that HLB means W.A. of Atlas Powder, Inc. of the United States. C. Griffin named Hydrophile Lyophile Balance and is a value obtained by indexing the balance between the hydrophilic group and the lipophilic group contained in the surfactant molecule as a characteristic value. It means that the lower the HLB value, the more lipophilic, while the higher the HLB value, the higher the hydrophilicity.

  Various additives can be blended in the hard coat layer of the present invention as required. Examples thereof include fluorine and silicon compounds for imparting water repellency, antifoaming agents for improving coatability and appearance, and antistatic agents and coloring dyes and pigments.

  In the present invention, the hard coat layer is formed by applying a coating liquid containing an ionizing radiation curable compound, particles, a photopolymerization initiator, and a surfactant in an organic solvent, followed by curing on a base film. It is preferable.

  As a method for laminating the hard coat layer, a known method may be mentioned, and a method in which the coating liquid is applied and dried on a base film and then cured is preferable. As a coating method, there are known coating methods such as a gravure coating method, a kiss coating method, a dip method, a spray coating method, a curtain coating method, an air knife coating method, a blade coating method, a reverse roll coating method, a bar coating method, and a lip coating method. Can be mentioned. Among these, a gravure coating method, particularly a reverse gravure method, which can be applied by a roll-to-roll method and can be applied uniformly, is preferable.

  As a method of dissolving or dispersing the ionizing radiation curable compound, particles, photopolymerization initiator and the like contained in the coating solution in an organic solvent, a method of stirring and dispersing them under heating is preferable. By heating the coating solution, the solubility of the ionizing radiation curable compound, particles and photopolymerization initiator can be improved. Therefore, the deterioration of the coating appearance due to undissolved materials can be suppressed.

  A well-known thing can be used for a disperser. Specific examples include a ball mill, a sand mill, an attritor, a roll mill, an agitator, a colloid mill, an ultrasonic homogenizer, a homomixer, a pearl mill, a wet jet mill, a paint shaker, a butterfly mixer, a planetary mixer, and a Henschel mixer.

  The concentration of the solid content of the ionizing radiation curable compound, particles, photopolymerization initiator and the like contained in the coating solution is preferably 5% by mass or more and 70% by mass. By adjusting the concentration of the solid content of the coating liquid to 5% by mass or more, it is possible to suppress a decrease in productivity due to a long drying time after coating. On the other hand, by adjusting the concentration of the solid content of the coating solution to 70% by mass or less, it is possible to prevent deterioration in leveling properties due to an increase in the viscosity of the coating solution and accompanying deterioration in coating appearance. From the viewpoint of coating appearance, the solid content concentration of the coating liquid, the type of organic solvent, and the type of surfactant are adjusted so that the viscosity of the coating liquid is in the range of 0.5 cps to 300 cps. It is preferable.

  The thickness of the hard coat layer after coating and curing depends on the degree of elongation during molding, but it is preferable that the thickness of the hard coat layer after molding be 0.5 μm or more and 50 μm or less. Specifically, the lower limit of the thickness of the hard coat layer before molding is preferably 0.6 μm or more, and more preferably 1.0 μm or more. Further, the upper limit of the thickness of the hard coat layer before molding is preferably 100 μm or less, more preferably 80 μm or less, further preferably 60 μm or less, and further preferably 20 μm or less. When the thickness of the hard coat layer is less than 0.6 μm, it is difficult to obtain hard coat properties. Conversely, when the thickness exceeds 100 μm, the hard coat layer tends to be poorly cured or curled due to cure shrinkage.

  When pre-drying is required, such as when an organic solvent is blended in the coating solution, known hot air drying, infrared heaters and the like can be used as a method of applying on the base film and drying, but hot air with a fast drying speed is used. Drying is preferred.

  The drying temperature after coating is preferably 40 ° C. or higher and 120 ° C. or lower, and particularly preferably the lower limit is 45 ° C. or higher and the upper limit is 80 ° C. or lower. If it is less than 40 degreeC, the organic solvent contained in a coating liquid cannot fully be removed, and problems, such as brushing, may generate | occur | produce. On the other hand, when the temperature exceeds 120 ° C., minute defects of the coating film such as minute coating removal from bubbles, minute repellency, and cracks are likely to occur, and the appearance may be poor. In addition, the film shrinks strongly due to heat, and the flatness of the film deteriorates due to heat wrinkles, so that uniform stretching cannot be obtained during molding, or local stretching occurs and the film breaks. Becomes defective.

  The tension of the film applied during drying is preferably 50 N / m or more and 300 N / m or less, particularly preferably the lower limit is 100 N / m or more and the upper limit is 250 N / m or less. When the tension of the film is less than 50 N / m, the traveling film meanders and it is impossible to apply the coating solution. On the other hand, when it exceeds 300 N / m, wrinkles are generated in the film, and the flatness is deteriorated and the appearance of the wound film is deteriorated. Furthermore, when the base film is a film having a low temperature and excellent moldability, the film is stretched in the traveling direction during drying and contracts in the width direction, and in the worst case, a problem arises in productivity such as breaking.

  In the present invention, a hard coat layer, an antistatic layer, an easy adhesion layer, an adhesive layer, an easy slip layer, an electromagnetic wave absorption layer, a dye, a pigment, etc., as long as the effect of the present invention is not impaired on the surface not provided with the hard coat layer. Other functions such as a resin layer containing a dye may be added.

In the present invention, the hard coat layer is formed by irradiating the coating solution with ultraviolet rays. As the integrated quantity of light to be irradiated, preferably 50 mJ / cm ² or more 1000 mJ / cm ² or less, and more preferably the lower limit is 300 mJ / cm ² or more, the upper limit is 700 mJ / cm ² or less. Note that it is desirable to perform irradiation in a nitrogen gas atmosphere because oxygen inhibition is reduced and scratch resistance is improved. When the integrated light quantity is less than 50 mJ / cm ² , the polymerization reaction of the ionizing radiation curable compound is not promoted, and the surface hardness of the hard coat layer is significantly reduced. When the integrated light quantity exceeds 1000 mJ / cm ² , the base film may be deformed due to the influence of heat. The integrated light amount in the present invention can be measured by “UVR-T35” manufactured by Topcon.

  Further, when the coating solution is cured with an electron beam, the irradiation dose is preferably 5 kGy or more and 100 kGy or less, and more preferably the upper limit is 30 kGy or more and the lower limit is 70 kGy or less. When it is less than 5 kGy, the polymerization reaction of the ionizing radiation curable compound is not promoted, and the surface hardness of the hard coat layer is significantly reduced. When it exceeds 100 kGy, the lifetime of the electron beam irradiation tube is remarkably reduced, which is not preferable in terms of production cost.

(Hard coat film for molding)
The molding hard coat film of the present invention is a film having excellent surface hardness. Specifically, in the case of a molding hard coat film using a biaxially oriented polyester film containing a copolymerized polyester as a base film, the measured value of pencil hardness is preferably H or more, and more preferably 2H or more. Particularly preferred. Here, the pencil hardness was evaluated according to JIS-K5600.

  As a method for adjusting the surface hardness, the content of mono- or bifunctional ionizing radiation-curable compounds in the ionizing radiation-curable compound contained in the coating solution for forming the hard coat layer and the ionizing radiation-curable compound having an amino group The content can be changed depending on the amount of particles, the amount of particles in the hard coat layer, and the thickness of the hard coat layer.

  The hard coat film for molding of the present invention is a film having excellent scratch resistance. Specifically, in the case of a molding hard coat film using a biaxially oriented polyester film containing a copolymerized polyester as a base film, although it depends on the base film, steel of # 0000 with a load of 500 gf in accordance with JIS-K5600. The surface is reciprocated 20 times with wool, and the presence or absence of scratches and the extent of the scratches are visually observed. The deep scratches are preferably a small amount of 10 or less, and more preferably no deep scratches at all.

  As a method for adjusting the scratch resistance, the content of the monofunctional or bifunctional ionizing radiation curable compound in the ionizing radiation curable compound contained in the coating solution for forming the hard coat layer or the ionizing radiation curable type having an amino group. It can be changed depending on the content of the compound and the amount of particles present in the hard coat layer.

  The molding hard coat film of the present invention is a film excellent in moldability. Specifically, in the case of a hard coat film for molding using a biaxially oriented polyester film containing a copolymerized polyester as a base film, the elongation is 10 at both room temperature and the actual film temperature of 160 ° C. % Or more, preferably 20% or more, and particularly preferably 30% or more. Here, the elongation means that a hard coat film for molding was cut into a strip shape having a length of 10 mm and a width of 150 mm, and when the actual film temperature was pulled at 160 ° C., cracks or whitening occurred in the hard coat layer. The stretching ratio at the time was defined as the degree of elongation (%).

  As a method for adjusting the moldability (elongation), the content of mono- or bifunctional ionizing radiation-curable compound in the ionizing radiation-curable compound contained in the coating solution for forming the hard coat layer or ionization having an amino group It can be changed depending on the content of the radiation curable compound and the amount of particles present in the hard coat layer.

  The molding hard coat film of the present invention preferably has transparency when printing is performed on the surface on which the hard coat layer is not laminated. Specifically, although it varies depending on the base film, in the case of a molding hard coat film using a biaxially oriented polyester film containing a copolymerized polyester as the base film, the haze is preferably 5% or less. The method for adjusting the haze can be changed depending on the abundance of particles in the hard coat layer.

  When the hard coat film for molding of the present invention is subjected to a printing process on a surface on which the hard coat layer is not laminated, it is preferable that there is no coloring. Specifically, although it varies depending on the base film, in the case of a hard coat film for molding using a biaxially oriented polyester film containing a copolyester as a base film, the value of the color tone b * may be 2.0 or less. preferable. As a method for adjusting the color tone b *, the color tone b * is changed depending on the content of the ionizing radiation-curable compound having an amino group in the ionizing radiation-curable compound contained in the coating solution for forming the hard coat layer and the amount of the photoinitiating polymer added. be able to. Here, the color tone b * is obtained by measuring the color tone b * value with a C light source and a viewing angle of 2 degrees using a color difference meter (manufactured by Nippon Denshoku Industries Co., Ltd., ZE-2000), and averaging the five measurement values. Value.

(Hard coat film roll for molding)
The molding hard coat film roll of the present invention is obtained through a step of continuously winding a long molding hard coat film in a roll shape around a cylindrical core. By using the hard coat film roll for molding, productivity at the time of processing can be improved, and further, it can contribute to the stability of the quality of the molded body. The length of the molding hard coat film roll obtained by continuously winding the long molding hard coat film into a roll on a cylindrical core is not particularly limited depending on the application, but is preferably 50 m or more and 5000 m or less, 100 m or more and 3000 m or less is more preferable. When the winding length is short, for example, the frequency of switching the hard coat film for molding at the time of processing the printed layer in the subsequent process is increased and workability is deteriorated. On the other hand, when the winding length is long, the molding hard coat film expands and contracts due to the external environmental temperature, and winding tightening occurs, resulting in a poor appearance of the core.

  The width of the hard coat film roll for molding varies depending on the application and is not particularly limited, but is preferably 100 mm or more and 2000 mm or less, more preferably 500 mm or more and 1500 mm or less from the viewpoint of workability.

  The cylindrical core around which the hard coat film for molding is wound is preferably a plastic core. When a commonly used paper core is used, paper dust or the like is generated and tends to adhere to the hard coat layer and become defective. As the plastic core, known ones can be preferably used, but a polypropylene core and an FRP core are preferable in terms of strength. The size of the cylindrical core is preferably 3 to 6 inches in diameter. When a core having a small diameter is used, the winding core is wrinkled and the handling property in the subsequent process becomes poor. On the other hand, when the diameter is large, the roll diameter becomes large and the handling property becomes poor.

  In order to wind the molding hard coat film around the core, it is preferable to start winding after fixing the molding hard coat film to the core via a double-sided tape. When a double-sided tape is not used, winding deviation is likely to occur during winding or during transportation. Although a well-known thing can be used as a double-sided tape, what has an adhesion layer on both surfaces of a plastic film is preferable at the point of generation | occurrence | production of paper dust, and an intensity | strength. The thickness of the double-sided tape is preferably 5 μm or more and 50 μm or less. When it is thin, the strength is lowered and workability is deteriorated, and the fixing force of the film is lowered. On the other hand, when the thickness is thick, the flatness of the hard coat film for molding the core portion becomes poor due to a step due to the tape.

  In this invention, it is preferable to provide an unevenness | corrugation (emboss) to the both ends of the width direction of the hard-coat film for a shaping | molding. By imparting irregularities, it becomes difficult to leave marks due to the double-sided tape at the core, and the functionality described above laminated on the hard coat layer and the base film surface layer on the opposite side or on the base film is given. The part which contacts with the layer which fell is reduced, and the storage stability in a roll form becomes favorable. The lower limit of the height of the unevenness is preferably 10 μm, more preferably 15 μm. On the other hand, the upper limit of the height of the unevenness is preferably 40 μm, more preferably 35 μm. When the height of the unevenness is too low, the effect of improving the storage stability in the roll form due to the unevenness is reduced. On the other hand, if the height of the unevenness is too high, winding deviation or the like is likely to occur during transportation. A publicly known method can be used as a method of giving unevenness. Specifically, a method of pressing the metal roll having protrusions on the surface to give irregularities can be mentioned. In addition, it is preferable to give uneven | corrugated processing to a base film previously, before forming a hard-coat layer on a base film.

(Molded body)
The molding hard coat film of the present invention is a molding material that is molded using a molding method such as vacuum molding, pressure molding, mold molding, press molding, laminate molding, in-mold molding, drawing molding, bending molding, and stretch molding. It is suitable as. In the case of molding using the molding hard coat film of the present invention, the hard coat layer follows the deformation during molding and no cracks are generated, and the surface hardness and scratch resistance can be maintained.

  The thickness of the hard coat layer of the molded body formed by molding the above-described hard coat film for molding is preferably 0.5 μm or more and 50 μm or less, and particularly preferably 0.5 μm or more and 10 μm or less. When the thickness of the hard coat layer of the molded body is less than 0.5 μm, hard coat properties cannot be obtained, and when heat is applied to the molded body in terms of heat resistance, the hard film cannot follow the shrinkage of the base film. The surface of the coat layer becomes rough like a wave, and the appearance is impaired. On the other hand, when it exceeds 50 μm, there is no difference in the surface hardness at the thickness of the hard coat layer beyond that, and the merit is reduced in terms of quality.

  The molded body molded in this way has a hard coat layer to compensate for surface hardness, so it is mounted at a position where it touches the outside and is required to have scratch resistance. It can be suitably used as a molding member such as a building material, a decorative board, a decorative steel plate, and a transfer sheet.

  Hereinafter, the present invention will be described in detail by way of examples. The film properties obtained in each example were measured and evaluated by the following methods.

(1) Elongation The obtained hard coat film for molding was cut into a strip-shaped sample piece having a length of 10 mm and a width of 150 mm. In an environment where the actual temperature of the film sample piece is 160 ° C., while visually observing the appearance, the film is gripped at both ends and pulled at a test speed of 250 mm / min, and when the hard coat layer is cracked or whitened, The length was measured.
When the length of the film sample piece before the test was a and the length of the film sample piece after the test was b, the elongation was calculated by the following formula.
Elongation (%) = (b−a) × 100 / a
Here, it was judged that those having an elongation of 10% or more were excellent in moldability, and those having an elongation of 30% or more were particularly excellent in moldability.

(2) Pencil hardness The pencil hardness of the hard coat layer of the obtained molding hard coat film was measured according to JIS-K5600. The indentation (scratch) was judged visually.
Here, those having a pencil hardness of H or higher were judged to have excellent surface hardness, and those having a pencil hardness of 2H or higher were judged to have particularly excellent surface hardness.

(3) Scratch resistance The scratch resistance of the hard coat layer of the obtained molding hard coat film was measured according to JIS-K5600. The hard coat layer surface was reciprocated 20 times with # 0000 steel wool at a load of 500 gf, and the presence or absence of scratches and the extent of the scratches were visually observed. The rank was determined according to the following criteria based on the observation results. The scratch resistance rank was C or higher, and there was scratch resistance, and those of B or higher were judged to have good scratch resistance.
A: There is no generation of scratches or thin scratches are observed in a small amount.
B: Although a thin wound is observed, a deep wound is not observed.
C: Narrow scratches are observed, and a small amount of deep scratches are also observed.
D: A lot of deep scratches are observed.

(4) Color tone b *
The color tone b * value of the obtained hard coat film for molding was measured using a color difference meter (manufactured by Nippon Denshoku Industries Co., Ltd., ZE-2000), and the color tone b * value was measured at a viewing angle of 2 degrees with a C light source. The measured values were averaged.

(5) Pencil hardness after molding, thickness of hard coat layer In the elongation evaluation of (1) above, by stopping pulling immediately before the occurrence of cracks, a molded body after stretch molding was obtained. The pencil hardness after molding was evaluated by the evaluation method (2). Further, the spectral reflectance at the center of the film sample piece (molded body) after molding is obtained from a spectrophotometer (manufactured by Shimadzu Corporation, UV-3150 type), and the peak valley method is calculated from the waveform at a wavelength of 400 nm to 600 nm. Using this, the thickness of the hard coat layer was calculated. The refractive index of the hard coat layer required at that time is to prepare a single film of the hard coat layer from the hard coat coating solution of each example and comparative example, and use an Abbe refractometer (NAR-1T SOLID, manufactured by Atago). Asked.

(6) Glass transition temperature Based on JIS K7121, using a differential scanning calorimeter (Seiko Instruments Co., Ltd., DSC6200), the temperature was raised at a rate of 20 ° C / min over a temperature range of 25 to 300 ° C, and from the DSC curve The obtained extrapolated glass transition start temperature was defined as the glass transition temperature.

(7) Interference fringe improvement (iris color)
The obtained hard coat film for molding was cut into an area of 10 cm (film width direction) × 15 cm (film longitudinal direction) to prepare a sample film. A black glossy tape (manufactured by Nitto Denko Corporation, vinyl tape No. 21; black) was bonded to the surface opposite to the hard coat layer surface of the obtained sample film. The sample film was observed with the hard coat surface as the upper surface and a three-wavelength daylight white color (National Palook, FL 15EX-N 15W) as a light source. The results of visual observation were ranked according to the following criteria.
○: Iridescent color is not seen △: Slightly irisy color is seen ×: Clear iris-like color is observed

(Polyester resin polymerization)
In a stainless steel autoclave equipped with a stirrer, a thermometer, and a partial reflux condenser, 186 parts by mass of dimethyl terephthalate, 186 parts by mass of dimethyl isophthalate, 23.7 parts of dimethyl 5-sodium sulfoisophthalate, 137 of neopentyl glycol Mass parts, 191 parts by mass of ethylene glycol, and 0.5 parts by mass of tetra-n-butyl titanate were charged, and a transesterification reaction was performed from 160 ° C. to 220 ° C. over 4 hours. Next, the temperature was raised to 255 ° C., and the pressure of the reaction system was gradually reduced, followed by reaction for 1 hour 30 minutes under a reduced pressure of 29 Pa to obtain a copolymerized polyester resin (A-1). The obtained copolyester resin was light yellow and transparent.

  In the same manner, copolymer polyester resins (A-2, A-3, A-4) having different compositions were obtained. Table 1 shows the results of the composition and weight average molecular weight measured by NMR for these copolyester resins.

Hereinafter, Examples 6 and 7 will be read as Reference Examples 6 and 7, respectively.
Example 1
(1) Preparation of polyester aqueous dispersion In a reactor equipped with a stirrer, a thermometer and a reflux device, 20 parts by mass of polyester resin (A-1) and 15 parts by mass of ethylene glycol monobutyl ether are added and heated at 100 ° C. , Stirred to dissolve the resin. After the resin was completely dissolved, 65 parts by mass of water was gradually added to the polyester solution while stirring. After the addition, the solution was cooled to room temperature while stirring to prepare an aqueous dispersion (B-1) of milky white polyester having a solid content of 20% by mass. Similarly, using the polyester resins (A-2) to (A-4) instead of the polyester resin (A-1), an aqueous dispersion was prepared, and the aqueous dispersions (B-2) to (B-) were respectively obtained. 4).

(2) Preparation of aqueous coating liquid 40 parts by mass of the obtained polyester aqueous dispersion (B-1), 44 parts by mass of hydroxybis (lactato) titanium (manufactured by Matsumoto Pharmaceutical Co., Ltd., TC310) 18 parts by mass, water 150 parts by mass and 100 parts by mass of isopropyl alcohol were mixed, and 1% by mass of anionic surfactant (Naopelex No6F powder, manufactured by Kao Corporation), colloidal silica fine particles (manufactured by Catalyst Kasei Kogyo, Cataloid SI80P (average particle size 80 nm) 2% by mass of an aqueous dispersion was added as silica to the resin solids to prepare an aqueous coating solution (hereinafter abbreviated as aqueous coating solution (C-1)).

(2) Manufacture of film raw material The intrinsic viscosity is 0.69 dl / with 100 mol% of terephthalic acid unit as an aromatic dicarboxylic acid component and 40 mol% of ethylene glycol unit and 60 mol% of neopentyl glycol unit as diol components. g of copolymer polyester chip (A) and polyethylene terephthalate containing 0.04% by mass of silica having an intrinsic viscosity of 0.69 dl / g and an average particle diameter (SEM method, the same applies hereinafter) of 2.7 μm. Each chip (B) was dried. Furthermore, the chip (A) and the chip (B) were mixed so as to have a mass ratio of 25:75.

(3) Manufacture of polyester film Next, these chip mixtures were melt-extruded from the slit of the T-die at 270 ° C. with an extruder, rapidly cooled and solidified on a chill roll having a surface temperature of 40 ° C., and simultaneously applied to a chill roll using an electrostatic application method. An amorphous unstretched sheet was obtained while closely contacting.

  The obtained unstretched sheet was stretched 3.3 times at 90 ° C. in the longitudinal direction between the heating roll and the cooling roll.

Subsequently, the aqueous uniaxially stretched film (C-1) was dried on the obtained uniaxially stretched film and then applied to one side of the film by a roll coating method so that the weight became 0.5 g / m ² and dried at 130 ° C. for 3 seconds. Water was removed.

  Subsequently, by heating with a tenter at a setting of 100 ° C. and transversely stretching 3.8 times, heat treatment at 230 ° C. for 5 seconds while fixing the width, and further relaxing by 5% in the width direction at 205 ° C. A polyester film having a thickness of 100 μm was obtained.

(4) Production of molding hard coat film The following hard coat coating solution A was applied to the intermediate layer side of the obtained film using a wire bar so that the coating thickness after drying was 2 μm, and the temperature was 80 ° C. Was dried with hot air for 60 seconds and passed through a position 20 cm under a high-pressure mercury lamp with an output of 120 W / cm at a speed of 10 m / min to obtain a hard coat film for molding. The refractive index of the hard coat layer was 1.48.
(Hard coat coating solution A)
The following materials were mixed at the mass ratio shown below, and dissolved by stirring for 30 minutes or more. Subsequently, the undissolved material was removed using a filter having a nominal filtration accuracy of 1 μm to prepare a hard coat coating solution A.
・ Methyl ethyl ketone 64.48% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 2)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution B.
(Hard coat coating solution B)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 17.18% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 2.86% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 2.86% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 3)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution C.
(Hard coat coating solution C)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 8.02 mass%
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 7.44% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 7.44% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

Example 4
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution D.
(Hard coat coating solution D)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 21.75 mass%
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 0.58% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 0.57% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 5)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution E.
(Hard coat coating solution E)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 1.15% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 0.58% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 21.17% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 6)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution F.
(Hard coat coating solution F)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 21.75 mass%
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 1.15% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 7)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution G.
(Hard coat coating solution G)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 1.15% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 21.75% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 8)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution H.
(Hard coat coating solution H)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 1.15% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Dimethylaminoethyl methacrylate 21.75% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained hard coat film for molding had a large amount of added amine compound, so that coloring was noticeably not preferred, but the moldability, surface hardness, and scratch resistance were all good. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

Example 9
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution I.
(Hard coat coating solution I)
・ Methyl ethyl ketone 64.48% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Diethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DE, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 10)
A hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer in Example 1 was changed to the following hard coat coating solution J.
(Hard coat coating solution J)
・ Methyl ethyl ketone 64.48% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ N-vinylformamide 5.72% by mass
(Arakawa Chemical, Beam Set 770, 1 functional group)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 11)
A hard coat film for molding was obtained in the same manner as in Example 1, except that the hard coat coating solution for forming the hard coat layer in Example 1 was changed to the following hard coat coating solution K.
(Hard coat coating solution K)
・ Methyl ethyl ketone 67.93 mass%
-Pentaerythritol triacrylate 11.58 mass%
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.79% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.79% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 7.72% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.16% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 12)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution L.
(Hard coat coating solution L)
・ Methyl ethyl ketone 4.24% by mass
-Pentaerythritol triacrylate 6.22 mass%
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 3.12% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 3.12% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
Silica fine particles 82.73% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 0.55% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicon surfactant 0.02% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 13)
A hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer in Example 1 was changed to the following hard coat coating solution M.
(Hard coat coating solution M)
・ Methyl ethyl ketone 71.46% by mass
-Pentaerythritol triacrylate 11.72% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.86% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.86% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
Silica fine particles 3.90% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.17% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 14)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution N.
(Hard coat coating solution N)
-Pentaerythritol triacrylate 5.28% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 2.64% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 2.64% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 88.88% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 0.55% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicon surfactant 0.02% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 15)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution O.
(Hard coat coating solution O)
・ Methyl ethyl ketone 58.76% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 17.17% by mass
(Made by Fuso Chemical Industries, PL2L-MEK, solid content ratio: 20%, average particle size: 20 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 16)
A hard coat film for molding was obtained in the same manner as in Example 1, except that the hard coat coating solution for forming the hard coat layer in Example 1 was changed to the following hard coat coating solution P.
(Hard coat coating solution P)
・ Methyl ethyl ketone 58.76% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 17.17% by mass
(Manufactured by Fuso Chemical Industries, PL30L-MEK, solid content ratio: 20%, average particle size: 297 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 17)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution Q.
(Hard coat coating solution Q)
・ Methyl ethyl ketone 58.76% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 17.17% by mass
(Nippon Shokubai Co., Ltd., Seahoster KE-E50, solid content ratio: 20%, average particle size: 511 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 18)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution R.
(Hard coat coating solution R)
・ Methyl ethyl ketone 72.50% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Melamine / formaldehyde condensate fine particles 3.43 mass%
(Nippon Shokubai, Eposter S, average particle size: 196 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 19)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution S.
(Hard coat coating solution S)
・ Methyl ethyl ketone 75.08 mass%
・ Pentaerythritol triacrylate 11.85% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.93 mass%
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.92% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
-Photopolymerization initiator 1.19% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 20)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1, except that the thickness of the hard coat layer after application and curing was 1.1 μm.

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 21)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1, except that the thickness of the hard coat layer after coating and curing was 50 μm.

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 22)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1, except that the thickness of the hard coat layer after coating and curing was 0.5 μm.

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. However, the surface hardness of the molded body molded from the obtained molding hard coat film was slightly poor. This is due to the fact that the thickness of the hard coat layer is reduced to a value outside the range where the surface hardness can be maintained by molding. The obtained results are shown in Table 2.

(Example 23)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1, except that the thickness of the hard coat layer after coating and curing was 60 μm.

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 2.

(Example 24)
48 parts by mass of polyester aqueous dispersion (B-2), 44 parts by mass of hydroxybis (lactato) titanium (manufactured by Matsumoto Pharmaceutical Co., Ltd., TC310) 15 parts by mass, 150 parts by mass of water and 100 parts by mass of isopropyl alcohol Furthermore, 1% by mass of anionic surfactant (Naopelex No6F powder, manufactured by Kao Corporation) and colloidal silica fine particles (manufactured by Catalytic Chemical Industry, Cataloid SI80P; average particle size 80 nm) in water dispersion Was added in an amount of 2% by mass as silica with respect to the resin solid content to prepare an aqueous coating solution (hereinafter abbreviated as aqueous coating solution (C-2)). Using this aqueous coating solution, a biaxially stretched film and a hard coat film having an intermediate layer on one side were obtained in the same manner as in Example 1. The evaluation results are shown in Table 2.

(Example 25)
Polyester aqueous dispersion (B-3) 12 parts by mass, diisopropoxybis (triethanolaminato) titanium 80% by mass solution (manufactured by Matsumoto Pharmaceutical Co., Ltd., TC400) 17 parts by mass, water 150 parts by mass and isopropyl alcohol 100 parts by mass were mixed, and anionic surfactant (Neopelex No6F powder, manufactured by Kao Corporation) was 1% by mass with respect to the coating liquid, colloidal silica fine particles (catalyst chemical industry, Cataloid SI80P; average particle size) 80 nm) An aqueous dispersion was added in an amount of 2% by mass as silica with respect to the resin solids to prepare an aqueous coating solution (hereinafter abbreviated as an aqueous coating solution (C-3)). Using this aqueous coating solution, a biaxially stretched film and a hard coat film having an intermediate layer on one side were obtained in the same manner as in Example 1. The evaluation results are shown in Table 2.

(Example 26)
24 parts by weight of polyester aqueous dispersion (B-4), 11 parts by weight of diisopropoxybis (acetylacetonate) titanium, 150 parts by weight of water and 100 parts by weight of isopropyl alcohol were mixed, respectively, and an anionic surfactant ( 1% by mass of Neoperex No6F powder made by Kao Corporation and 2% by weight of colloidal silica fine particles (catalyst chemical industry, Cataloid SI80P; average particle size of 80 nm) as a silica with respect to the resin solid content. % Was added to prepare an aqueous coating solution (hereinafter abbreviated as aqueous coating solution (C-4)). Using this coating solution, a biaxially stretched film and a hard coat film having an intermediate layer on one side were obtained in the same manner as in Example 1. The evaluation results are shown in Table 2.

(Example 27)
32 parts by mass of a polyester aqueous dispersion (B-4), 10 parts by mass of zirconium acetate, 150 parts by mass of water and 100 parts by mass of isopropyl alcohol were mixed, and an anionic surfactant (Neopelex No6F powder manufactured by Kao Corporation) was mixed. ) 1% by mass with respect to the coating solution, and 2% by mass of colloidal silica fine particles (catalyst chemical industry, Cataloid SI80P; average particle size 80 nm) aqueous dispersion as silica with respect to the resin solids to prepare an aqueous coating solution. (Hereinafter abbreviated as aqueous coating solution (C-5)). Using this coating solution, a biaxially stretched film and a hard coat film having an intermediate layer on one side were obtained in the same manner as in Example 1. The evaluation results are shown in Table 2.

(Comparative Example 1)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the coating liquid for forming the hard coat layer was changed to the following hard coat coating liquid T.
(Hard coat coating solution T)
・ Methyl ethyl ketone 64.48% by mass
-Pentaerythritol triacrylate 22.90% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 made by Ciba Specialty)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good surface hardness, scratch resistance, and coloring, but had poor moldability and was poor as a molding hard coat film. The obtained results are shown in Table 2.

(Comparative Example 2)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution U.
(Hard coat coating solution U)
・ Methyl ethyl ketone 64.48% by mass
・ Tripropylene glycol diacrylate 11.45% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 11.45% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 made by Ciba Specialty)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability and coloring degree, but had poor surface hardness and scratch resistance, and was poor as a molding hard coat film. The obtained results are shown in Table 2.

(Comparative Example 3)
58 parts by mass of polyester aqueous dispersion (B-1), 150 parts by mass of water and 100 parts by mass of isopropyl alcohol were mixed, and an anionic surfactant (Naopelex No6F powder, manufactured by Kao Corporation) was added to the coating liquid. 1% by mass, colloidal silica fine particles (catalyst chemical industry, Cataloid SI80P; average particle size 80 nm) in water dispersion was added in an amount of 2% by mass as silica with respect to the resin solids to prepare an aqueous coating solution (hereinafter referred to as aqueous coating). Liquid (C-6)). Using this coating solution, a biaxially stretched film and a hard coat film having an intermediate layer on one side were obtained in the same manner as in Example 1. The evaluation results are shown in Table 2.

(Example 28)
In Example 1, a molding hard coat film was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution V.
(Hard coat coating solution V)
・ Methyl ethyl ketone 63.62% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
・ Ionizing radiation curable silicone compound polyether acrylate 0.86% by mass
(Germany Chemie Service, TEGO Rad2200N)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 3.

(Example 29)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution W.
(Hard coat coating solution W)
・ Methyl ethyl ketone 64.42% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
・ Ionizing radiation curable silicone compound polyether acrylate 0.06% by mass
(Germany Chemie Service, TEGO Rad2200N)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 3.

(Example 30)
In Example 1, a hard coat film for molding was obtained in the same manner as in Example 1 except that the hard coat coating solution for forming the hard coat layer was changed to the following hard coat coating solution X.
(Hard coat coating solution X)
・ Methyl ethyl ketone 61.62% by mass
・ Pentaerythritol triacrylate 11.45% by mass
(Manufactured by Shin-Nakamura Chemical, NK ester A-TMM-3LM-N, functional group number 3)
・ Tripropylene glycol diacrylate 5.73% by mass
(Shin Nakamura Chemical, NK Ester APG-200, 2 functional groups)
・ Dimethylaminoethyl methacrylate 5.72% by mass
(Kyoeisha Chemical Co., Ltd., light ester DM, functional group number 1)
・ Silica fine particles 11.45% by mass
(Nissan Chemical Industries, MEK-ST-L, solid content ratio: 30%, average particle size: 50 nm)
・ Ionizing radiation curable silicone compound polyether acrylate 2.86% by mass
(Germany Chemie Service, TEGO Rad2200N)
-Photopolymerization initiator 1.14% by mass
(Irgacure 184 manufactured by Ciba Specialty Chemicals)
・ Silicone-based surfactant 0.03% by mass
(Toray Dow Corning DC57)

  The obtained molding hard coat film had good moldability, surface hardness, scratch resistance, and degree of coloring, and was good as a molding hard coat film. Moreover, the surface hardness of the molded object molded from the obtained molding hard coat film was also good. The obtained results are shown in Table 3.

  Since the hard coat film for molding of the present invention has a hard coat layer to compensate for the surface hardness of the base film, the molded body formed by molding the hard coat film for molding of the present invention requires scratch resistance. It is suitable as a housing for portable appliances such as home appliances, automobile nameplates or building materials, mobile phones, audio, portable players / recorders, IC recorders, car navigation systems, PDAs, and notebook PCs. Also, in the manufacturing process of molding, by processing and laminating a hard coat layer on the base film before molding, it can contribute to improving productivity and quality stability, making a significant contribution to the industry. .

Claims (6)

It is a hard coat film for molding laminated in the order of at least a base film, an intermediate layer, and a hard coat layer,
The base film is a biaxially oriented polyester film containing a copolymerized polyester,
The intermediate layer comprises an aqueous polyester resin (A) and at least one of a water-soluble titanium chelate compound, a water-soluble titanium acylate compound, a water-soluble zirconium chelate compound, or a water-soluble zirconium acylate compound (B). Applying and drying an aqueous coating solution containing a resin composition having a mixing ratio (mass ratio) of (A) / (B) of 10/90 to 95/5 as a main constituent component,
The hard coat layer is formed by applying and curing a coating solution on the intermediate layer surface of the base film,
The coating solution contains at least an ionizing radiation curable compound having three or more functional groups, and a monofunctional and / or bifunctional ionizing radiation curable compound,
Wherein Ri der content of 5 wt% to 95 wt% of one and / or two functional ionizing radiation curable compound in the coating liquid ionizing radiation-curable compound contained in,
At least one is Ru der ionizing radiation curable compound having an amino group, a hard coat film for molding of ionizing radiation curable compounds contained in the coating liquid. In the hard coat layer, containing particles having an average particle size of 10 nm to 300 nm,
The hard coat film for molding according to claim 1, wherein the content of the particles in the hard coat layer is 5% by mass or more and 70% by mass or less. Including the ionizing radiation curable silicone resin in the hard coat layer,
The molding according to claim 1 or 2 , wherein the content of the ionizing radiation curable silicone resin in the hard coat layer is 0.15 parts by mass or more and 15 parts by mass or less with respect to 100 parts by mass of the ionizing radiation curable compound. Hard coat film. The aqueous polyester resin (A) is, according to claim 1 to 3 aromatic dicarboxylic acid component containing metal sulfonate is copolymerized polyester resin containing 1 to 10 mol% based on all the dicarboxylic acid component of the polyester The hard coat film for molding according to any one of the above. The hard coat film for molding according to any one of claims 1 to 4 , wherein the aqueous polyester resin (A) has a glass transition temperature of 40 ° C or higher. The molded object formed by shape | molding the hard-coat film for shaping | molding in any one of Claims 1-5 .