JP2017052921A - Film - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an acrylic resin film having antiblocking property while maintaining beautiful appearance, excellent transparency and processability of the acrylic resin film.SOLUTION: There is provided a film consisting of a resin composition containing an acrylic resin and a lubricant, where the lubricant is an acrylic crosslinked structure-containing graft copolymer, average particle diameter of the (meth)acrylic crosslinked polymer is 180 to 400 nm, the lubricant is contained at 0.1 to 4.5 wt.% based on 100 wt.% of the resin composition and is a graft copolymer having the acrylic crosslinked polymer obtained by polymerizing a monomer component (a) consisting of an acrylic acid alkyl ester (a-1) having C of an alkyl group of 1 to 12 of 60 to 100 wt.% and another monomer unit (a-2) having a copolymerizable double bond of 40 to 0 wt.% and a polyfunctional monomer (a-3) of 2.3 to 10 pts.wt. based on 100 pts.wt. of the monomer component (a).SELECTED DRAWING: None

Description

  The present invention relates to a film.

  Acrylic resin films have excellent transparency, weather resistance, gloss, and processability, and are therefore used industrially in various fields such as automobile interior and exterior members and building materials. In recent years, taking advantage of the excellent optical properties of acrylic resins, they have also been used as optical members.

  However, acrylic resin films tend to be in close contact with each other (blocking is likely to occur). Once in close contact, the films are stuck together, resulting in poor appearance and significantly reducing film manufacturability and handling.

  As a general means for preventing blocking, inorganic fine particles such as silicon oxide, titanium dioxide, calcium carbonate, talc, diatomaceous earth, and synthetic silica are added. However, although the anti-blocking performance can be improved, the transparency of the film tends to decrease. Therefore, it has been proposed to use silica particles having a specific particle size as an anti-blocking agent in order to suppress blocking of the acrylic resin film (Patent Document 1).

Patent No. 5,587,209

  However, when the anti-blocking property is imparted by the silica particles having a specific average particle diameter as in Patent Document 1, the particles are likely to cause an increase in fish eye due to a decrease in transparency of the film or poor dispersion of the anti-blocking agent. It is difficult to obtain an acrylic resin film that has both a sufficient appearance as a resin film and an anti-blocking property.

  Moreover, in order to give antiblocking property, when the addition part number of an antiblocking agent is increased, there exists a possibility that the mechanical elongation and intensity | strength of a film may fall.

  Then, an object of this invention is to provide the acrylic resin film which has antiblocking property, maintaining the beautiful external appearance of the acrylic resin film, the outstanding transparency, and workability.

  In view of the above circumstances, as a result of intensive studies by the present inventors, the graft copolymer containing a specific acrylic rubber is excellent while maintaining the excellent appearance and workability of the acrylic resin film. It was found that the anti-blocking property can be imparted and is effective as a lubricant, and the present invention has been completed.

That is, the present invention is a film comprising a resin composition containing an acrylic resin and a lubricant, wherein the lubricant is an acrylic crosslinked structure-containing graft copolymer, and the acrylic crosslinked structure-containing graft copolymer is The (meth) acrylic crosslinked polymer having an average particle size of 180 to 400 nm,
The present invention relates to a film containing the lubricant in an amount of 0.1 to 4.5% by weight in 100% by weight of the resin composition (hereinafter sometimes referred to as “the film of the present invention”).

  In the film of the present invention, the acrylic crosslinked structure-containing graft copolymer is an acrylic acid alkyl ester (a-1) having 1 to 12 carbon atoms in an alkyl group (a-1) of 60 to 100% by weight, and copolymerized therewith. Monomer component (a) comprising 40 to 0% by weight of another monomer unit (a-2) having a possible double bond, and polyfunctional monomer (a-3) (monomer A graft copolymer having an acrylic cross-linked polymer obtained by polymerizing component (a) (100 to 10 parts by weight with respect to 100 parts by weight) is preferable.

  In the film of the present invention, the acrylic cross-linked structure-containing graft copolymer has 60 to 100% by weight of a methacrylic acid ester having 1 to 4 carbon atoms in the alkyl group and a copolymerizable double bond. It is preferable that a polymer obtained by polymerizing a monomer component composed of 40 to 0% by weight of the above monomer has a structure in which the acrylic cross-linked polymer is graft-bonded.

  In the film of the present invention, the acrylic crosslinked structure-containing graft copolymer may be copolymerized with 40 to 100% by weight of alkyl methacrylate (c-1) having 1 to 4 carbon atoms in the alkyl group, and copolymerizable. A monomer component (c) comprising 0 to 60% by weight of another monomer having a double bond, and a crosslinked methacrylic polymer obtained by polymerizing a polyfunctional monomer (c-3) It is preferable that the graft copolymer has a structure in which at least a part thereof is covered with the acrylic cross-linked polymer.

  In the film of the present invention, the acrylic crosslinked structure-containing graft copolymer is an acrylic acid alkyl ester (a-1) having 1 to 12 carbon atoms in an alkyl group (a-1) of 60 to 100% by weight, and copolymerized therewith. Monomer component (a) comprising 40 to 0% by weight of another monomer (a-2) having a possible double bond, and a polyfunctional monomer (monomer component (a) 100% by weight In the presence of a cross-linked acrylic polymer obtained by polymerizing 2.3 to 10 parts by weight with respect to part, a monomer mixture containing a methacrylic acid ester having an alkyl group with 1 to 4 carbon atoms. It is preferably obtained by polymerization.

In the film of the present invention, the (meth) acrylic crosslinked structure-containing graft copolymer particles are:
(A-1) A monomer component comprising 40 to 100% by weight of an alkyl methacrylate having 1 to 4 carbon atoms in the alkyl group and 0 to 60% by weight of another monomer copolymerizable therewith. (C) and a polyfunctional monomer (0.01 to 10 parts by weight based on 100 parts by weight of the monomer component (c)) to obtain a methacrylic crosslinked polymer,
(A-2) In the presence of the methacrylic cross-linked polymer, 60 to 100% by weight of an alkyl acrylate ester (a-1) having an alkyl group having 1 to 12 carbon atoms, and copolymerizable therewith Other monomer (a-2) monomer component (a-2) comprising 40 to 0% by weight, and multifunctional monomer (2 per 100 parts by weight of monomer component (a) 3 to 10 parts by weight) to obtain an acrylic crosslinked polymer,
(A-3) In the presence of the acrylic cross-linked polymer, 60 to 100% by weight of an alkyl group having 1 to 4 carbon atoms in the alkyl group and a double bond copolymerizable therewith It is preferable that it is a thing obtained by superposing | polymerizing the monomer component (b) which consists of 40 to 0 weight% of these monomers.

  In the film of the present invention, the acrylic cross-linked structure-containing graft copolymer has a (meth) acrylic cross-linked polymer content of less than 60% by weight in 100% by weight of the acrylic cross-linked structure-containing graft copolymer. Is preferred.

  The laminate of the present invention is obtained by laminating the film of the present invention on a substrate.

  The film of the present invention has a beautiful appearance, excellent transparency, and processability of an acrylic resin film, reduces friction between films, and suppresses occurrence of blocking.

(Lubricant)
The film of the present invention is characterized by using an acrylic cross-linked graft copolymer (hereinafter sometimes simply referred to as “graft copolymer (A)”) as a lubricant.

  The acrylic cross-linked structure graft copolymer is a graft copolymer having an acrylic cross-linked polymer. Here, the graft copolymer generally includes forms referred to as a multistage polymer and a multilayer structure polymer (sometimes referred to as a core-shell polymer). A multi-stage polymer is a polymer obtained by polymerizing a monomer mixture in the presence of polymer particles, and a multilayer structure polymer is obtained by polymerizing a monomer mixture in the presence of polymer particles. It is a polymer having a polymer layer. Both refer to basically the same polymer, but the former specifies the polymer mainly by the production method, and the latter specifies the polymer mainly by the layer structure.

  By using the lubricant of the present invention, when formed into an acrylic resin film, the friction between the films is reduced and the blocking is suppressed without impairing the transparency and workability of the acrylic resin film.

  The crosslinked (meth) acrylic polymer is a crosslinked acrylic polymer obtained by polymerizing a monomer component containing an alkyl acrylate ester having an alkyl group with 1 to 12 carbon atoms and a polyfunctional monomer. It is preferable to have a coalescence. Specifically, 60 to 100% by weight of an alkyl acrylate ester (a-1) having 1 to 12 carbon atoms in the alkyl group, and another monomer having a double bond copolymerizable therewith (a -2) What is obtained by superposing | polymerizing the monomer component (a) which consists of 40 to 0 weight% and a polyfunctional monomer (a-3) is preferable.

  Examples of the alkyl acrylate ester (a-1) having 1 to 12 carbon atoms in the alkyl group include, for example, ethyl acrylate, n-butyl acrylate, n-octyl acrylate, 2-ethylhexyl acrylate, propyl acrylate, acrylic Examples include acid hexyl, cyclohexyl acrylate, and isobornyl acrylate. You may use these individually or in combination of 2 or more types. Especially, it is preferable that acrylic acid alkyl ester (a-1) contains n-butyl acrylate. In 100% by weight of acrylic acid alkyl ester (a-1), the ratio of n-butyl acrylate is preferably 50 to 100% by weight, more preferably 70 to 100% by weight, and still more preferably 90 to 100% by weight. .

  Although it does not specifically limit as another monomer (a-2) which has a double bond which can be copolymerized, The group which consists of a methacrylic acid ester, an aromatic vinyl-type monomer, and another copolymerizable monomer It is preferable to use at least one selected from Examples of the methacrylic acid ester include methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, t-butyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, octyl methacrylate, And methacrylic acid esters such as isobornyl methacrylate, phenyl methacrylate, and benzyl methacrylate. Of these, alkyl methacrylates having 1 to 4 carbon atoms in the alkyl group are preferred. These may be used alone or in combination of two or more, but it is particularly preferable that at least methyl methacrylate is contained. Examples of the aromatic vinyl monomer include styrene, α-methylstyrene, chlorostyrene, and other styrene derivatives. Only one of these may be used, or two or more may be used in combination. Other monomers having copolymerizable double bonds other than methacrylic acid esters and aromatic vinyl monomers include acrylic acid esters such as phenyl acrylate and benzyl acrylate, acrylonitrile, and methacrylonitrile. Unsaturated nitrile monomers, α, β-unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, olefin monomers such as vinyl acetate, ethylene and propylene, vinyl chloride, vinylidene chloride, vinylidene fluoride And halogenated vinyl monomers such as N-ethylmaleimide, N-propylmaleimide, N-cyclohexylmaleimide, and N-o-chlorophenylmaleimide. These may be used alone or in combination of two or more.

  The other monomer (a-2) having a copolymerizable double bond preferably contains an aromatic vinyl monomer and / or a methacrylic acid ester from the viewpoint of transparency.

  As the polyfunctional monomer (a-3), any of those known as a crosslinking agent or a crosslinking monomer can be used. The polyfunctional monomer is preferably allyl methacrylate, allyl acrylate, diallyl maleate, diallyl fumarate, diallyl itaconate, monoallyl maleate, monoallyl fumarate, butadiene, divinylbenzene or the like. These may be used alone or in combination of two or more. Among them, at least one of the polyfunctional monomers is preferably allyl methacrylate.

  A chain transfer agent may be used if necessary, and those listed below for the chain transfer agent can be used as well, and preferred chain transfer agents are also suitable. When a chain transfer agent is used, it may be the same as or different from the chain transfer agent used in the polymerization of the methacrylic polymer described later.

  The monomer component (а) is an acrylic acid alkyl ester (a-1) 60 to 100% by weight, and a monomer (a-2) having a double bond copolymerizable therewith 40 to 0% by weight It is preferable to contain. From the viewpoint of polymerizability, the acrylic acid alkyl ester (a-1) is more preferably 70 to 90% by weight, further preferably 75 to 90% by weight. The other monomer (a-2) having a copolymerizable double bond is more preferably 30 to 10% by weight, and further preferably 25 to 10% by weight. If the acrylic acid alkyl ester (a-1) is less than 60% by weight in 100% by weight of the monomer component (a), the transparency may be lowered.

  The amount of the polyfunctional monomer used is preferably 2.3 parts by weight or more and 10 parts by weight or less with respect to 100 parts by weight of the monomer component (a) from the viewpoint of antiblocking properties. More preferably, it is more preferably 2.7 parts by weight or more, and particularly preferably 2.9 parts by weight or more. 6 parts by weight or less is preferable, 5.5 parts by weight or less is more preferable, and 5 parts by weight or less is more preferable. When the amount of the polyfunctional monomer used is less than 2.3 parts by weight, the anti-blocking effect is not sufficiently exhibited, and when it exceeds 10 parts by weight, the transparency may be lowered.

  The graft copolymer (A) may further have another polymer (hard or soft polymer) on the center side. In the case of having a hard polymer, for example, a methacrylic crosslinked polymer obtained by polymerizing a monomer component containing a methacrylic acid alkyl ester whose alkyl group has 1 to 4 carbon atoms and a polyfunctional monomer. Is preferred. From the viewpoint of antiblocking properties, alkyl methacrylate (C-1) having an alkyl group having 1 to 4 carbon atoms of 40 to 100% by weight, and other monomer having a double bond copolymerizable therewith Monomer component (c) comprising 60 to 0% by weight of the body (c-2), and a polyfunctional monomer (c-3) (0 to 100 parts by weight of the monomer component (c)) 0.01 to 10 parts by weight) is preferably a methacrylic crosslinked polymer obtained by polymerization.

  Examples of the alkyl methacrylate having 1 to 4 carbon atoms in the alkyl group (c-1) include methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate and t-butyl methacrylate. It is done. These may be used alone or in combination of two or more, but it is particularly preferable that at least methyl methacrylate is contained.

  The monomer component (c) may contain another monomer (c-2) having a double bond copolymerizable with the alkyl methacrylate (c-1). Although it does not specifically limit as another monomer (c-2) which has a copolymerizable double bond, Acrylic acid ester, an aromatic vinyl-type monomer, and others which have a copolymerizable double bond It is preferable to use at least one selected from the group consisting of these monomers.

  Examples of the acrylate ester include ethyl acrylate, n-butyl acrylate, n-octyl acrylate, 2-ethylhexyl acrylate, hexyl acrylate, cyclohexyl acrylate, isobornyl acrylate, phenyl acrylate, and benzyl acrylate. can give. From the viewpoints of polymerizability and cost, acrylic acid alkyl esters are preferable, and alkyl alkyl esters having 1 to 12 carbon atoms in the alkyl group are more preferable. Only one of these may be used, or two or more may be used in combination. The acrylic ester may be the same as or different from the acrylic ester used in the alkyl acrylate ester (a-1). Examples of the aromatic vinyl monomer include styrene, α-methylstyrene, chlorostyrene, and other styrene derivatives. Only one of these may be used, or two or more may be used in combination. Other monomers having a copolymerizable double bond other than acrylic acid esters and aromatic vinyl monomers include, for example, hexyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, octyl methacrylate, methacrylic acid. Methacrylates such as isobornyl acid, phenyl methacrylate and benzyl methacrylate, unsaturated nitrile monomers such as acrylonitrile and methacrylonitrile, α, β-unsaturated carboxylic acids such as acrylic acid, methacrylic acid and crotonic acid, Vinyl acetate, olefin monomers such as ethylene and propylene, vinyl halides such as vinyl chloride, vinylidene chloride, vinylidene fluoride, N-ethylmaleimide, N-propylmaleimide, N-cyclohexylmaleimide, N- o-Chlorophe And maleimide monomers such as nilmaleimide. Any of these may be used alone or in combination of two or more.

  As another monomer (c-2) having a double bond capable of copolymerization, from the viewpoint of polymerizability and cost, an alkyl alkyl ester having 1 to 12 carbon atoms and / or an aromatic vinyl is used. It is preferable that a system monomer is included.

  The monomer component (c) is 40 to 100% by weight of the methacrylic acid alkyl ester (c-1) and another monomer (c-2) containing a copolymerizable double bond 0 to 60% by weight. % Content is preferable. From the viewpoint of transparency, the methacrylic acid alkyl ester (c-1) is more preferably 50 to 100% by weight, and further preferably 60 to 100% by weight. The other monomer (c-2) containing a copolymerizable double bond is more preferably 0 to 50% by weight, and further preferably 0 to 40% by weight. Specifically, the monomer component (c) is 40 to 100% by weight of methacrylic acid alkyl ester (c-1), 0 to 35% by weight of acrylic acid ester, 0 to 10% by weight of aromatic vinyl monomer, And it is preferable that it is 0-15 weight% of the other monomer which has a copolymerizable double bond, and other copolymerizable monomers. From the viewpoint of thermal stability, alkyl methacrylate ester (c-1) 40 to 99.9% by weight, acrylic acid ester 0.1 to 35% by weight, aromatic vinyl monomer 0 to 10% by weight, and It is more preferable that the other monomer having a copolymerizable double bond is 0 to 15% by weight. If it is this range, the thermal stability of a graft copolymer (A) can be made high, and the resin composition of this invention can also be used for high temperature shaping | molding.

  As a polyfunctional monomer (c-3), what was illustrated to the said polyfunctional monomer (a-3) can be used similarly, and a preferable illustration is also the same. In addition, the polyfunctional monomer may be the same as or different from the compound used in the polyfunctional monomer (a-3).

  The polyfunctional monomer is preferably used in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the monomer component (c), and more preferably 0.01 to 7 from the viewpoint of polymerizability. Parts by weight, more preferably 0.01 to 5 parts by weight, and most preferably 0.01 to 2 parts by weight.

  The monomer component (c) and the polyfunctional monomer (c-3) may be polymerized in the presence of a chain transfer agent, and generally known chain transfer agents can be used as the chain transfer agent. Specific examples of the chain transfer agent include n-butyl mercaptan, n-octyl mercaptan, n-hexadecyl mercaptan, n-dodecyl mercaptan, t-dodecyl mercaptan, t-tetradecyl mercaptan, n-tetradecyl mercaptan, sec-butyl. Mercaptan, mercaptan compounds such as sec-dodecyl mercaptan, 2-ethylhexyl thioglycolate, ethylene glycol dithioglycolate, trimethylolpropane tris (thioglycolate), thioglycolic acid ester such as pentaerythritol tetrakis (thioglycolate), thio Examples include phenol, tetraethylthiuram disulfide, pentanephenylethane, acrolein, methacrolein, allyl alcohol, carbon tetrachloride, and ethylene bromide. That. From the viewpoint of handleability, tertiary mercaptans such as t-dodecyl mercaptan, n-dodecyl mercaptan and thiophenol are preferred. Further, from the viewpoint of thermal stability, primary alkyl mercaptan compounds and / or secondary alkyl mercaptan compounds are preferable, and n-octyl mercaptan and n-dodecyl mercaptan are more preferable. These may be used alone or in combination of two or more.

  In the present invention, the weight ratio of the monomer component (c) and the monomer component (a) is such that the monomer component (c): monomer component (a) is from the viewpoint of productivity. It is preferable that it is 10: 90-60: 40, 30:70 is more preferable, and 35:65 is further more preferable.

  The form in which the graft copolymer (A) has the above-mentioned methacrylic crosslinked polymer on the center side is obtained by polymerizing the monomer component (c) and the polyfunctional monomer (c-3). It is formed by polymerizing the monomer component (a) and the polyfunctional monomer (a-3) in the presence of a crosslinked polymer to obtain an acrylic crosslinked polymer. The graft copolymer (A) may have a structure in which at least a part of the methacrylic crosslinked polymer is coated with the acrylic crosslinked polymer. The acrylic cross-linked polymer only needs to cover at least a part of the methacrylic cross-linked polymer, and a part of the acrylic cross-linked polymer may enter the inside of the methacrylic cross-linked polymer. Of course, the acrylic cross-linked polymer may cover the entire methacrylic cross-linked polymer, and includes a form covering the entire methacrylic cross-linked polymer. In addition, a polymerized product that is not involved in the coating of the methacrylic crosslinked polymer, which is generated when the acrylic crosslinked polymer is polymerized, may be generated, and such a polymerized product is also included.

  In the present application, the (meth) acrylic cross-linked polymer in the acrylic cross-linked structure-containing graft copolymer (graft copolymer (A)) is composed of the above-mentioned acrylic cross-linked polymer and methacrylic cross-linked copolymer (A). When it has a cross-linked polymer, it refers to an aggregate of an acrylic cross-linked polymer and a methacrylic cross-linked polymer, and when it does not contain a methacrylic cross-linked polymer, it refers to an acrylic cross-linked polymer. In addition, the acrylic cross-linked structure-containing graft copolymer of the present invention is not limited to the above-mentioned acrylic cross-linked polymer as long as the effects of the present invention are not impaired. Furthermore, you may contain. When another soft polymer (acrylic cross-linked polymer) is included, the above-mentioned cross-linked polymer refers to an aggregate that also contains another acrylic cross-linked polymer.

The graft copolymer (A) of the present invention is obtained by polymerizing a monomer mixture containing a methacrylic ester as a main component in the presence of the above-mentioned acrylic crosslinked polymer. Specifically, in the presence of the above-mentioned acrylic cross-linked polymer, methacrylic acid alkyl ester (b-1) having 1 to 4 carbon atoms in the alkyl group, and copolymerizable double What is obtained by polymerizing the monomer component (b) comprising 40 to 0% by weight of another monomer (b-2) having a bond is a preferred embodiment. The alkyl group has 1 to 4 carbon atoms. Examples of the methacrylic acid alkyl ester (b-1) include those described in the above methacrylic acid alkyl ester (c-1). The methacrylic acid alkyl ester (b-1) may be the same as or different from the compound used as the methacrylic acid alkyl ester (c-1).

  Although it does not specifically limit as another monomer (b-2) which has a double bond which can be copolymerized, It is preferable to use at least 1 type chosen from an acrylate ester and another copolymerizable monomer. .

  The acrylic ester preferably contains an alkyl alkyl ester having 1 to 12 carbon atoms in terms of polymerizability and cost. As the acrylic ester, those exemplified as the above-mentioned acrylic ester can be used similarly, and preferable examples are also the same. Examples of other monomers having a copolymerizable double bond other than acrylic acid esters include aromatic vinyl monomers such as styrene, α-methylstyrene, chlorostyrene, and other styrene derivatives, methacrylic acid, and the like. Hexyl, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, octyl methacrylate, isobornyl methacrylate, phenyl methacrylate, methacrylic ester such as benzyl methacrylate, unsaturated nitrile monomers such as acrylonitrile and methacrylonitrile, acrylic acid , Α, β-unsaturated carboxylic acids such as methacrylic acid and crotonic acid, vinyl acetate, olefinic monomers such as ethylene and propylene, vinyl halide monomers such as vinyl chloride, vinylidene chloride and vinylidene fluoride, N-ethylmaleimide, N Propyl maleimide, N- cyclohexyl maleimide, and the like maleimide monomers such as N-o-chlorophenyl maleimide. Any of these may be used alone or in combination of two or more.

  The monomer component (b) is not particularly limited, but from the viewpoint of dispersibility and transparency of the graft copolymer (A), 100% by weight of the monomer component (b) is an alkyl methacrylate ( The content of b-1) is preferably 60 to 100% by weight, more preferably 70 to 100% by weight, and still more preferably 80 to 100% by weight. The other monomer (b-2) having a copolymerizable double bond is preferably contained in an amount of 40 to 0% by weight, more preferably 0 to 30% by weight, and further preferably 0 to 20% by weight. Specifically, methacrylic acid alkyl ester (b-1) 60 to 100% by weight, acrylic acid ester 40 to 0% by weight, and other monomers having a copolymerizable double bond 10 to 0% by weight It is preferable that When the methacrylic acid alkyl ester (b-1) is less than 60% by weight in 100% by weight of the monomer mixture component (b), there may be a problem in productivity.

  A polyfunctional monomer may be used during the polymerization of the monomer component (b). As the polyfunctional monomer, those listed above for the polyfunctional monomer can be used in the same manner, and preferred polyfunctional monomers are also suitable. Although the usage-amount of a polyfunctional monomer is not specifically limited, 0-10 weight part is preferable with respect to 100 weight part of monomer components (b), 0.1-5 weight part is more preferable, More preferably, 3 parts by weight.

  During the polymerization of the monomer component (b), a chain transfer agent may be used as necessary. As the chain transfer agent, those mentioned above for the chain transfer agent can be used in the same manner, and preferable chain transfer agents are also suitable. When a chain transfer agent is used, it may be the same as or different from the chain transfer agent used in the polymerization of the above-mentioned crosslinked acrylic polymer and / or the above-mentioned methacrylic crosslinked polymer.

  The monomer component (b) may be polymerized in one stage, or may be polymerized in two or more stages. When the polymerization is carried out in two or more stages, the monomer / mixing ratio of the monomer component in each stage may be changed. For example, methacrylic acid alkyl ester (b-1) 60 to 100% by weight, acrylic acid ester 40 to 0% by weight, and other monomers having a copolymerizable double bond 0 to 5% by weight After the polymerization of the monomer component (b1), the methacrylic acid alkyl ester (b-1) is 40 to 100% by weight, the acrylic acid ester is 60 to 0% by weight, and another single monomer having a copolymerizable double bond. It may be obtained by polymerizing the monomer component (b2) comprising 0 to 5% by weight of the body. In addition, the monomer components (b1) and (b2) may be polymerized in the reverse order.

  The preferred form of the graft copolymer (A) is a methacrylic acid alkyl ester (b-1) in which the alkyl group has 1 to 4 carbon atoms in the presence of the acrylic crosslinked polymer and a copolymer thereof. It is obtained by polymerizing the monomer component (b) composed of the monomer (b-2). The graft copolymer (A) has a structure in which a polymer having the structural units (b-1) and (b-2) as described above is grafted to the acrylic crosslinked polymer. A part of the polymer exists as a polymerization product that is not graft-bonded to the crosslinked acrylic polymer, and includes the polymerization product. In addition, when the acrylic cross-linked polymer in the graft copolymer (A) is in a form in which at least a part of the above methacrylic cross-linked polymer is coated, a part of the polymer is the methacrylic cross-linked polymer. It may also be grafted to the coalescence. Moreover, when it has another soft or hard crosslinked polymer other than the said acrylic type crosslinked polymer or a methacryl type crosslinked polymer, the said polymer may graft-bond to the said other soft or hard crosslinked polymer. These forms are also included in the graft copolymer (A).

  From the viewpoint of the dispersibility of the graft copolymer (A), the graft copolymer (A) of the present invention has a content ratio of the acrylic cross-linked polymer in the graft copolymer (A) of the graft copolymer (A). A) It is preferable that it is less than 60 weight% in 100 weight%. Specifically, the monomer constituting the acrylic cross-linked polymer in a total amount of 100% by weight of the monomer component (monomer component excluding the polyfunctional monomer) constituting the graft copolymer (A). It is a content rate of a component (monomer component except a polyfunctional monomer). Specifically, when the graft copolymer (A) has the acrylic cross-linked copolymer and the methacrylic cross-linked polymer, the monomer component constituting the graft copolymer (A) (polyfunctional monomer) The content ratio of the monomer component (a) and the monomer component (c) in a total amount of 100% by weight of the monomer component excluding the monomer). The content is preferably less than 60% by weight, more preferably 55% by weight or less, and even more preferably 50% by weight or less. From the viewpoint of productivity, 20% by weight or more is preferable, and 30% by weight or more is more preferable.

  As described above, the graft copolymer (A) which is the lubricant of the present invention may have a soft polymer-hard polymer two-stage polymer structure (two-layer structure (core-shell structure)), and A structure having three or more stages of polymerization such as a hard polymer-soft polymer-hard polymer or soft polymer-soft polymer-hard polymer having a hard or soft layer in the center (structure of three layers or more) Also good. Here, “soft” means that the glass transition temperature of the polymer is less than 20 ° C., and “hard” means that the glass transition temperature of the polymer is preferably 20 ° C. or higher. “Hard” and “soft” glass transition temperatures are calculated using Fox's equation using the values described in the Polymer Hand Book (J. Brandrup, Interscience 1989). It is.

For example, (A-1) from 40 to 100% by weight of an alkyl methacrylate having 1 to 4 carbon atoms in the alkyl group and 0 to 60% by weight of another monomer having a copolymerizable double bond The monomer component (c) and the polyfunctional monomer (0.01 to 10 parts by weight with respect to 100 parts by weight of the monomer component (c)) are polymerized to obtain a methacrylic crosslinked polymer. ,
(A-2) In the presence of the crosslinked methacrylic polymer, 60 to 100% by weight of an alkyl acrylate ester having 1 to 12 carbon atoms in the alkyl group, and other monomers copolymerizable therewith A monomer component (a) composed of 40 to 0% by weight and a polyfunctional monomer (2.3 to 10 parts by weight with respect to 100 parts by weight of the monomer component (a)) are polymerized, To obtain a crosslinked polymer,
(A-3) A monomer having 60 to 100% by weight of a methacrylic acid alkyl ester having 1 to 4 carbon atoms in the presence of the acrylic crosslinked polymer and a copolymerizable double bond Examples include a graft copolymer (three-stage polymer of hard polymer-soft polymer-hard polymer) formed by polymerizing the monomer component (b) comprising 40 to 0% by weight. Graft copolymer (soft polymer-hard polymer two-stage weight) obtained by performing the polymerization steps (A-2) and (A-3) without performing the polymerization step (A-1). Or a polymerization step of another hard polymer or soft polymer may be included between the polymerization steps (A-1) to (A-3).

  The graft copolymer (A) is not particularly limited, but can be produced by a known emulsion polymerization method, emulsion-suspension polymerization method, suspension polymerization method, bulk polymerization method, solution polymerization method or dispersion polymerization method. The emulsion polymerization method is particularly preferred. Examples of the surfactant used in the emulsion polymerization include sodium alkyl sulfonate, sodium alkylbenzene sulfonate, sodium dioctyl sulfosuccinate, sodium lauryl sulfate, fatty acid sodium, and polyoxyethylene lauryl ether sodium phosphate. Anionic surfactants such as phosphate ester salts, nonionic surfactants and the like are shown. These surfactants may be used alone or in combination of two or more. From the viewpoint of improving the thermal stability of the resin composition of the present invention, it is particularly preferable to perform polymerization using a phosphate ester salt (alkali metal or alkaline earth metal) such as sodium polyoxyethylene lauryl ether phosphate. .

  As an initiator in the polymerization of the graft copolymer (A), known initiators such as organic peroxides, inorganic peroxides, and azo compounds can be used. Specifically, for example, t-butyl hydroperoxide, 1,1,3,3-tetramethylbutyl hydroperoxide, succinic acid peroxide, peroxymaleic acid t-butyl ester, cumene hydroperoxide, benzoyl peroxide Organic peroxides such as oxides, inorganic peroxides such as potassium persulfate and sodium persulfate, and oil-soluble initiators such as azobisisobutyronitrile are also used. These may be used alone or in combination of two or more. These initiators include reducing agents such as sodium sulfite, sodium thiosulfate, sodium formaldehyde sulfoxylate, ascorbic acid, hydroxyacetone acid, ferrous sulfate, ferrous sulfate and disodium ethylenediaminetetraacetate It may be used as a combined ordinary redox initiator.

  The organic peroxide can be added by a known addition method such as a method of adding to a polymerization system as it is, a method of adding a mixture to a monomer, a method of adding a dispersion in an aqueous emulsifier solution, and the like. From the viewpoint of transparency, a method of adding a mixture to a monomer or a method of adding it by dispersing in an aqueous emulsifier solution is preferable.

  The organic peroxide is an organic reducing agent such as divalent iron salt and / or formaldehyde sulfoxylate soda, reducing sugar ascorbic acid or the like from the viewpoint of polymerization stability and particle size control. It is preferably used as a redox initiator combined with a system reducing agent.

  The surfactant used for the emulsion polymerization is not particularly limited, and any surfactant for normal emulsion polymerization can be used. Specifically, for example, anionic surfactants such as sodium alkyl sulfonate, sodium alkyl benzene sulfonate, sodium dioctyl sulfosuccinate, sodium lauryl sulfate, sodium fatty acid, alkyl phenols, aliphatic alcohols and propylene oxide, Nonionic surfactants such as reaction products with ethylene oxide are shown. These surfactants may be used alone or in combination of two or more. Furthermore, if necessary, a cationic surfactant such as an alkylamine salt may be used.

  The average particle size of the graft copolymer (A) is preferably 190 to 500 nm, and more preferably 200 to 400 nm. The average particle diameter here is determined using light scattering at a wavelength of 546 nm using a U-5100 type ratio beam spectrophotometer manufactured by Hitachi High-Technologies Corporation.

  The latex-like graft copolymer (A) is spray-dried or, as is generally known, coagulated by adding a salt or an acid, and then filtered, washed and dried after heat treatment. As a result, a powdery graft copolymer (A) is obtained. If necessary, an anti-aging agent or an ultraviolet absorber that is usually added during coagulation may be added.

  The graft copolymer (A) is a lubricant capable of achieving both transparency and anti-blocking properties when the average particle diameter of the (meth) acrylic crosslinked polymer of the graft copolymer (A) is 180 to 400 nm. Can work effectively. 200-350 nm is preferable and 200-300 nm is more preferable. Here, the average particle diameter of the acrylic cross-linked polymer is determined using light scattering at a wavelength of 546 nm using a U-5100 type ratio beam spectrophotometer manufactured by Hitachi High-Technologies Corporation.

  When the graft copolymer (A) of the present invention is used as a lubricant and blended with an acrylic resin having a good balance of appearance, transparency, weather resistance, gloss, workability, etc., the excellent appearance and transparency unique to the acrylic resin A film excellent in anti-blocking property between films can be formed without impairing properties and strength.

  The content of the graft copolymer (A) in the resin composition of the present invention is not particularly limited, but is 0.1 to 4.5% by weight in 100% by weight of the resin composition. In light of the balance between transparency and antiblocking property, the content is more preferably 0.15% by weight or more, and further preferably 0.2% by weight or more. 4 wt% or less is more preferable, 3.5 wt% or less is more preferable, and 3 wt% or less is still more preferable.

  The graft copolymer (A) in the present invention preferably has a graft ratio of 20% or more, more preferably 30% or more, and still more preferably 60% by weight. If the graft ratio is less than 20%, the dispersibility of the graft copolymer (A) is lowered, which may cause the generation of fish eyes. The graft ratio of the graft copolymer (A) is an index representing the weight ratio of the graft-bonded monomer components in the graft copolymer, and is determined by the following formula.

  1 g of graft copolymer is dissolved in 40 ml of methyl ethyl ketone, and centrifuged for 1 hour at 3000 rpm using a centrifuge (manufactured by Hitachi Koki Co., Ltd., CP60E) to separate insoluble and soluble components. To do.

Graft ratio (%) = {(weight of insoluble matter of methyl ethyl ketone−weight of monomer constituting (meth) acrylic crosslinked polymer / weight of monomer constituting (meth) acrylic crosslinked polymer}} × 100
The weight of the monomer constituting the (meth) acrylic crosslinked polymer in this case is a monomer component excluding the polyfunctional monomer from all monomers. For example, when the graft copolymer (A) has the above-mentioned methacrylic crosslinked polymer and acrylic crosslinked polymer, it refers to the total amount of the monomer component (a) and the monomer component (b).

(Acrylic resin)
The resin composition of the present invention contains an acrylic resin. The acrylic resin may be a resin having a vinyl monomer containing a methacrylic ester as a constituent unit, and a known acrylic resin can be used. Those containing a structural unit derived from a methacrylic acid ester are preferred. From the viewpoint of thermal stability, those containing 30% by weight or more of a methacrylic acid alkyl ester unit having 1 to 4 carbon atoms in the alkyl group as a constituent unit are preferred, It is more preferable to include at least%. A typical example of the acrylic resin is a (co) polymer composed of 30 to 100% by weight of methyl methacrylate and 70 to 100% by weight of another copolymerizable monomer. Other copolymerizable monomers include, for example, methyl acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, hexyl (meth) acrylate, (meth) acrylic acid (Meth) acrylate esters such as cyclohexyl, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, isobornyl (meth) acrylate, phenyl (meth) acrylate, benzyl (meth) acrylate, styrene, Aromatic vinyl monomers such as o-methylstyrene, m-methylstyrene, p-methylstyrene, α-methylstyrene, acrylonitrile, acrylonitrile-styrene copolymers, unsaturated nitrile monomers such as cellulose acetate and methacrylonitrile Polymer, acrylic acid, methacrylic acid, crotonic acid, etc. α, β-unsaturated carboxylic acids, vinyl acetate, olefinic monomers such as ethylene and propylene, vinyl halide monomers such as vinyl chloride, vinylidene chloride and vinylidene fluoride, N-ethylmaleimide, N-propyl And maleimide monomers such as maleimide, N-cyclohexylmaleimide, and N-o-chlorophenylmaleimide. These may be used alone or in combination of two or more.

  From the viewpoint of optical properties, appearance, weather resistance, and heat resistance, the acrylic resin preferably has 30 to 100% by weight, more preferably 50 to 99.9% by weight, and still more preferably methyl methacrylate as a structural unit. The monomer that is contained in an amount of 50 to 98% by weight and copolymerizable with methyl methacrylate is preferably 70 to 0% by weight, more preferably 50 to 0.1% by weight, and further preferably 50 to 2% by weight. In addition, it is preferable that a polyfunctional monomer is not included from a viewpoint of workability and an external appearance property.

  The acrylic resin used in the resin composition of the present invention preferably has a glass transition temperature of 90 ° C. or higher from the viewpoint of heat resistance during use. When applied to applications requiring excellent heat resistance, such as optical applications, acrylic resins having excellent heat resistance are suitable, and specifically, the glass transition temperature is preferably 100 ° C. or higher, preferably 115 ° C. The above is more preferable, 118 ° C. or higher is more preferable, 120 ° C. or higher is further preferable, and 125 ° C. or higher is even more preferable.

  Examples of the acrylic resin having excellent heat resistance include acrylic resins and methacrylic resins having a ring structure in the main chain. Examples of the ring structure include a maleimide structure (including an N-substituted maleimide structure), a glutarimide structure, a glutaric anhydride structure, a maleic anhydride structure, and a lactone ring structure. Moreover, the acrylic resin which contains a (meth) acrylic acid structural unit in a molecule | numerator is also mentioned. Specifically, an acrylic resin (maleimide acrylic resin), glutarimide acrylic resin, lactone ring-containing acrylic resin, hydroxyl group and / or carboxyl group in which an N-substituted maleimide compound is copolymerized as a copolymerization component. Partial hydrogenation obtained by partial hydrogenation of aromatic ring of styrene polymer obtained by polymerizing acrylic resin, methacrylic resin, styrene monomer and other monomers copolymerizable therewith Examples thereof include styrene polymers, acrylic polymers containing cyclic acid anhydride repeating units such as glutaric anhydride units and maleic anhydride units. Among these, the lactone ring-containing acrylic resin, maleimide acrylic resin, glutarimide acrylic resin, glutaric anhydride structure-containing acrylic resin because the heat resistance of the film improves when molded into an acrylic resin film In addition, a maleic anhydride structure-containing acrylic resin is preferable, and among them, a glutarimide acrylic resin, a maleimide acrylic resin, and a glutaric anhydride structure-containing acrylic resin are particularly preferable because of excellent optical characteristics. A glutarimide acrylic resin and a maleimide acrylic resin may be used in combination. Since both resins are excellent in compatibility, they can maintain high transparency, have excellent optical characteristics, have high thermal stability, and can also have solvent resistance.

  Although the compounding quantity of acrylic resin is not specifically limited, It is preferable that it is 30-99.9 weight% in the total amount of 100 weight% of acrylic resin composition.

(Rubber component)
The resin composition containing an acrylic resin and a lubricant in the present invention may contain a rubber component in order to improve moldability. A rubber-like polymer can be used as the rubber component, and examples thereof include a polymer having a glass transition temperature of less than 20 ° C. Specific examples include butadiene-based crosslinked polymers, (meth) acrylic crosslinked polymers, and organosiloxane-based crosslinked polymers. Among these, a (meth) acrylic crosslinked polymer (acrylic rubbery polymer) is particularly preferable in terms of weather resistance (light resistance) and transparency of the film. Examples of the acrylic rubber-like polymer include ABS resin rubber and ASA resin rubber.

  As the rubber component, a graft copolymer containing a rubbery polymer is also preferable. The graft copolymer generally includes forms referred to as a multistage polymer, a multilayer structure polymer, and a core / shell polymer.

  From the viewpoint of transparency and the like, an acrylic graft copolymer containing the acrylic rubber-like polymer shown below (hereinafter simply referred to as “rubber-containing graft copolymer”) can be preferably used. The rubber-containing graft copolymer can be obtained by polymerizing a monomer mixture containing methacrylic acid ester as a main component in the presence of an acrylic rubber-like polymer.

  As the acrylic rubbery polymer, a monomer mixture containing 60 to 100% by weight of an acrylate ester and 0 to 40% by weight of another monomer having a double bond copolymerizable therewith ( X) (100% by weight in total) and those obtained by polymerizing polyfunctional monomers are preferred. The monomer mixture (X) and the polyfunctional monomer may be used by mixing them all at once, and the composition of the monomer mixture and the polyfunctional monomer may be changed in two or more stages. May be used (ie, two or more stages of polymerization may be performed). As the acrylate ester, the other monomer having a copolymerizable double bond, and the polyfunctional monomer, those described above can be used similarly, and preferable examples are also suitable.

The rubber-containing graft copolymer may have a soft polymer-hard polymer two-stage polymer structure (two-layer structure (core / shell structure)), and further a hard or soft layer having a hard or soft layer at the center. A structure having three or more stages of polymerization (structure of three layers or more) such as a polymer-soft polymer-hard polymer or a soft polymer-soft polymer-hard polymer may be used.
The rubber-containing graft copolymer is not particularly limited, and a known emulsion polymerization method, emulsion-suspension polymerization method, suspension polymerization method, bulk polymerization method, solution polymerization method or dispersion polymerization method can be applied. The emulsion polymerization method is particularly preferable from the viewpoint of a large structure adjustment range. The initiator, surfactant, separation / recovery method, and the like are not particularly limited, and those described in the above graft copolymer (A) are also included.

  In the resin composition of the present invention, the content of the rubber-containing graft copolymer is such that the rubber elastic body in the rubber-containing graft copolymer is 0.1% by weight to 50% by weight in 100% by weight of the resin composition. The content is preferably 0.1% by weight or more, more preferably 5% by weight or more, still more preferably 10% by weight or more. It is more preferably 40% by weight or less, and further preferably 35% by weight or less.

  The resin composition of the present invention may be blended with other thermoplastic resins as necessary, for example, a polyethylene terephthalate resin, a polybutylene terephthalate resin, or the like. The blending method is not particularly limited, and a known method can be used.

  In the resin composition of the present invention, if necessary, an inorganic pigment or an organic dye is used for coloring, and an antioxidant, a heat stabilizer, or an ultraviolet absorber for further improving the stability to heat or light. , UV stabilizers, etc., or antibacterial agents, deodorizing agents, lubricants and the like may be added singly or in combination of two or more.

  Especially, an ultraviolet absorber is preferably used when improving a weather resistance. Examples of the UV absorber include commonly used benzotriazole UV absorbers, 2-hydroxybenzophenone UV absorbers, and salicylic acid phenyl ester UV absorbers. Specifically, as a benzotriazole ultraviolet absorber, 2,2′-methylenebis [4- (1,1,3,3-tetramethylbutyl) -6- (2H-benzotriazol-2-yl) phenol] 2- (5-methyl-2-hydroxyphenyl) -2H-benzotriazole, 2- [2-hydroxy-3,5-bis (α, α-dimethylbenzyl) phenyl] -2H-benzotriazole, 2- ( 3,5-di-tert-butyl-2-hydroxyphenyl) -2H-benzotriazole, 2- (3-tert-butyl-5-methyl-2-hydroxyphenyl) -5-chloro-2H-benzotriazole, 2 -(3,5-di-tert-butyl-2-hydroxyphenyl) -5-chloro-2H-benzotriazole, 2- (3,5-di-tert-a Examples include mil-2-hydroxyphenyl) -2H-benzotriazole, 2- (2'-hydroxy-5'-tert-octylphenyl) -2H-benzotriazole. Specific examples of 2-hydroxybenzophenone-based ultraviolet absorbers include 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-octyloxybenzophenone, 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxy-4 Examples include '-chlorobenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone and the like. Specific examples of salicylic acid phenyl ester ultraviolet absorbers include p-tert-butylphenyl salicylic acid ester and p-octylphenyl salicylic acid ester. These ultraviolet absorbers may be used alone or in combination of two or more.

  In this invention, when mix | blending a ultraviolet absorber, 0.1 to 3 weight% or more is preferable normally with respect to 100 weight% of resin compositions, More preferably, it is 0.3 to 3 weight%. is there.

  The resin composition of the present invention is particularly useful as a film, and is satisfactorily processed by, for example, an ordinary melt extrusion method such as an inflation method, a T-die extrusion method, a calendar method, or a solvent casting method. In addition, when forming a film, if necessary, both surfaces of the film are brought into contact with a roll or a metal belt at the same time, particularly by bringing into contact with a roll or a metal belt heated to a temperature equal to or higher than the glass transition temperature. It is also possible to obtain a better film. In addition, depending on the purpose, film lamination and biaxial stretching can be used to modify the film.

(Film formation)
The film of the present invention may be obtained by a known molding method of the resin composition of the present invention. For example, it can be molded satisfactorily by an ordinary melt extrusion method such as an inflation method, a T-die extrusion method, a calendar method, or a solvent casting method. Among these, the melt extrusion method is preferable from the viewpoint of productivity.

  Hereinafter, as an embodiment of the method for producing a film of the present invention, a method for producing a film by molding by a melt extrusion method will be described in detail.

  When the resin composition of the present invention is formed into a film by a melt extrusion method, first, the resin composition of the present invention is supplied to an extruder, and the resin composition is heated and melted. When supplying to an extruder, you may supply each component of a resin composition with a granular form, or what made the resin composition pelletized with the extruder previously to an extruder.

  The resin composition of the present invention is preferably pre-dried before being supplied to the extruder. By performing such preliminary drying, foaming of the resin extruded from the extruder can be prevented.

  Although the method of preliminary drying is not particularly limited, for example, the raw material (that is, the resin composition of the present invention) can be formed into pellets or the like and can be performed using a hot air dryer or the like.

  The extruder for forming the resin composition of the present invention into a film preferably has one or more devolatilizers for removing volatile components generated during heating and melting. By having a deaeration device, it is possible to reduce deterioration of the film appearance due to resin foaming and decomposition degradation reaction.

  In melt extrusion for forming the resin composition of the present invention into a film, it is preferable to supply an inert gas such as nitrogen or helium to the cylinder of the extruder along with the supply of the resin material. By supplying the inert gas, it is possible to reduce the concentration of oxygen in the system and to reduce deterioration in appearance and quality such as decomposition, crosslinking, and yellowing due to oxidative deterioration.

  Next, the resin composition heated and melted in the extruder is supplied to the T die through a gear pump and a filter. At this time, if a gear pump is used, the uniformity of the extrusion amount of the resin can be improved and thickness unevenness can be reduced. On the other hand, if a filter is used, the foreign material in a resin composition can be removed and the film excellent in the external appearance without a defect can be obtained.

  As the type of filter, it is preferable to use a stainless steel leaf disc filter capable of removing foreign substances from the molten polymer, and it is preferable to use a fiber type, a powder type, or a composite type thereof as the filter element. The filter can be suitably used for an extruder or the like used for pelletization or film formation.

  Next, the resin composition supplied to the T die is extruded from the T die as a sheet-like molten resin. The sheet-like molten resin is cooled using a plurality of cooling rolls. Usually, the T die is arranged so that the molten resin contacts the first cast roll on the most upstream side (the one closer to the die). In general, two cooling rolls are used. The temperature of the cast roll is preferably 50 ° C to 160 ° C, more preferably 60 ° C to 120 ° C. Thereafter, the film is peeled off from the cast roll, passed through a nip roll, and then wound up.

  In addition, as a method of bringing the resin into close contact with the cast roll, a touch roll method, a nip roll method, an electrostatic application method, an air knife method, a vacuum chamber method, a calendar method, a sleeve method, and the like can be mentioned. An appropriate method is selected. In the case of forming an optical film with a small optical distortion, it is desirable to use a touch roll system, and in particular, an elastic roll having a double sleeve structure of a metal sleeve. The temperature of the touch roll is preferably 40 ° C to 120 ° C, more preferably 50 ° C to 100 ° C.

  If necessary, the surface of the film can be formed by simultaneously contacting (sandwiching) both sides of the film with a roll or a metal belt, particularly by contacting the roll or metal belt heated to a temperature close to the glass transition temperature. It is also possible to obtain a film having better properties.

  One of the two cooling rolls sandwiching the sheet-like molten resin is a rigid metal roll having a smooth surface, and the other has a metal elastic outer cylinder having a smooth surface and capable of elastic deformation. A flexible roll is preferred.

  With such a rigid metal roll and a flexible roll having a metal elastic outer cylinder, the sheet-like molten resin is sandwiched and cooled to form a film, thereby correcting minute surface irregularities and die lines. Thus, a film having a smooth surface and thickness unevenness of 5 μm or less can be obtained.

  Even when the rigid metal roll and the flexible roll are used, since the surface of each cooling roll is metal, when the film to be formed is thin, the surfaces of the cooling roll come into contact with each other. The outer surface may be scratched, or the cooling roll itself may be damaged.

  Therefore, when forming a film by sandwiching a sheet-like molten resin with two cooling rolls as described above, a film is obtained by first sandwiching and cooling the sheet-like molten resin with the two cooling rolls. . Here, “cooling roll” is used to include “touch roll” and “cooling roll”.

(the film)
The film of the present invention preferably has a total light transmittance (60 μm) of 85% or more, more preferably 88% or more, and still more preferably 90% or more. If the total light transmittance is in the above-mentioned range, the transparency is high, and therefore, it is suitable for optical members, decoration applications, interior applications, and vacuum forming applications that require light transmission.

  The film of the present invention preferably has a glass transition temperature of 80 ° C. or higher, more preferably 90 ° C. or higher, and further preferably 100 ° C. or higher. In view of obtaining an acrylic resin film having excellent heat resistance, the glass transition temperature is preferably 115 ° C. or higher, more preferably 120 ° C. or higher, and even more preferably 124 ° C. or higher.

  The film of the present invention preferably has a haze (60 μm) of 2.0% or less, more preferably 1.5% or less, and even more preferably 1.3% or less. If the haze is in the above-described range, the transparency is high, and thus it is suitable for optical members that require light transmission, decoration applications, interior applications, and vacuum forming applications.

  The film of the present invention can also be used as an optical film. In particular, when applied to a polarizer protective film, it is preferable that the optical anisotropy is small. In particular, it is preferable that not only the optical anisotropy in the in-plane direction (length direction, width direction) of the acrylic resin film but also the optical anisotropy in the thickness direction is small. That is, it is preferable that both the in-plane retardation and the absolute value of the thickness direction retardation are small. The absolute value of the in-plane retardation is preferably 10 nm or less, more preferably 6 nm or less, and further preferably 3 nm or less. The absolute value of the thickness direction retardation is preferably 20 nm or less, more preferably 10 nm or less, and even more preferably 5 nm or less. An acrylic resin film having such a phase difference is suitable as a polarizer protective film provided in a polarizing plate of a liquid crystal display device.

  The phase difference is an index value calculated based on birefringence, and the in-plane phase difference (Re) and the thickness direction phase difference (Rth) can be calculated by the following equations, respectively. In an ideal film that is completely optically isotropic in the three-dimensional direction, both the in-plane retardation Re and the thickness direction retardation Rth are zero.

Re = (nx−ny) × d
Rth = ((nx + ny) / 2−nz) × d
In the above formula, nx, ny, and nz are respectively the in-plane stretching direction (polymer chain orientation direction) as the X axis, the direction perpendicular to the X axis as the Y axis, and the thickness direction of the film as the Z axis. , And represents the refractive index in the respective axial directions. D represents the thickness of the film, and nx-ny represents orientation birefringence. In the case of a melt-extruded film, the MD direction is the X axis, and in the case of a stretched film, the stretch direction is the X axis.

The film of the present invention has an orientation birefringence value of preferably −2.6 × 10 ^{−4 to} 2.6 × 10 ⁻⁴ , more preferably −2.1 × 10 ^{−4 to} 2.1 × 10 ^{−. 4} , more preferably −1.7 × 10 ^{−4 to} 1.7 × 10 ⁻⁴ , even more preferably −1.6 × 10 ^{−4 to} 1.6 × 10 ⁻⁴ , and even more preferably −1.5. × 10 ^{−4 to} 1.5 × 10 ⁻⁴ , more preferably −1.0 × 10 ^{−4 to} 1.0 × 10 ⁻⁴ , particularly preferably −0.5 × 10 ^{−4 to} 0.5 × 10 ^-4, most preferably ^{-0.2 × 10 -4 ~0.2 × 10 -4} . When the orientation birefringence is within the above range, stable optical characteristics can be obtained without causing birefringence during molding. It is also very suitable as an optical film used for liquid crystal displays and the like.

(Stretching)
The film of the present invention has high toughness and high flexibility even as an unstretched film, but may be further stretched, thereby improving the mechanical strength of the acrylic resin film and improving the film thickness accuracy. it can.

  When the film of the present invention is stretched, the resin composition of the present invention is once formed into an unstretched film, and then subjected to uniaxial stretching or biaxial stretching to produce a stretched film (uniaxially stretched film or biaxial). Stretched film) can be produced.

  In the present specification, for convenience of explanation, a film after the resin composition of the present invention is formed into a film and before being stretched, that is, an unstretched film is referred to as a “raw film”.

  When stretching the raw material film, the raw material film may be stretched immediately after the raw material film is formed, or after the raw material film is molded, the raw material film is temporarily stored or moved to stretch the raw material film. You may go.

  In addition, when the raw material film is stretched immediately after being formed into a raw material film, the state of the raw material film may be stretched in a very short time (in some cases, instantaneously) in the film manufacturing process. May be stretched after a certain period of time.

  When the film of the present invention is used as a stretched film, the raw material film only needs to maintain a film shape sufficient to be stretched, and does not have to be a complete film.

  The method for stretching the raw material film is not particularly limited, and any conventionally known stretching method may be used. Specifically, for example, transverse stretching using a tenter, longitudinal stretching using a roll, sequential biaxial stretching in which these are sequentially combined, and the like can be used. Moreover, the simultaneous biaxial stretching method which extends | stretches the length and the width | variety simultaneously can be used, or the method of performing the horizontal extending | stretching by a tenter can be used after performing roll vertical stretching.

  When the raw material film is stretched, it is preferable that the raw material film is once preheated to a temperature 0.5 to 5 ° C., preferably 1 to 3 ° C. higher than the stretching temperature, and then cooled and stretched to the stretching temperature.

  By preheating within the above range, the thickness of the raw material film can be maintained with high accuracy, and the thickness accuracy of the stretched film does not decrease and thickness unevenness does not occur. Further, the raw material film does not stick to the roll and does not loosen due to its own weight.

  On the other hand, if the preheating temperature of the raw material film is too high, there is a tendency that the raw material film sticks to the roll or is loosened by its own weight. In addition, if the difference between the preheating temperature and the stretching temperature of the raw material film is small, it tends to be difficult to maintain the thickness accuracy of the raw material film before stretching, the thickness unevenness increases, or the thickness accuracy tends to decrease.

  The stretching temperature when stretching the raw material film is not particularly limited, and may be changed according to the mechanical strength, surface property, thickness accuracy, and the like required for the stretched film to be produced.

  In general, when the glass transition temperature of the raw material film obtained by the DSC method is defined as Tg, the temperature range is preferably (Tg-30 ° C) to (Tg + 30 ° C), and (Tg-20 ° C) to ( Tg + 20 ° C. is more preferable, and a temperature range of (Tg) to (Tg + 20 ° C.) is more preferable.

  When the stretching temperature is within the above temperature range, thickness unevenness of the obtained stretched film can be reduced, and further, mechanical properties such as elongation, tear propagation strength, and fatigue resistance can be improved. Moreover, generation | occurrence | production of the trouble that a film adheres to a roll can be prevented.

  On the other hand, when the stretching temperature is higher than the above temperature range, the thickness unevenness of the stretched film obtained tends to be large, and the mechanical properties such as elongation, tear propagation strength, and fatigue resistance cannot be improved sufficiently. There is. Furthermore, there is a tendency that troubles such as the film sticking to the roll tend to occur.

  Further, when the stretching temperature is lower than the above temperature range, the resulting stretched film has a large haze, or in extreme cases, the process tends to cause problems such as tearing or cracking of the film. is there.

  When the raw material film is stretched, the stretch ratio is not particularly limited, and may be determined according to the mechanical strength, surface properties, thickness accuracy, and the like of the stretched film to be produced. Although it depends on the stretching temperature, the stretching ratio is generally preferably selected in the range of 1.1 to 3 times, more preferably in the range of 1.3 to 2.5 times. Preferably, it is more preferable to select in the range of 1.5 times to 2.3 times. If the draw ratio is within the above range, the mechanical properties such as the elongation rate of the film, tear propagation strength, and fatigue resistance can be greatly improved.

  The thickness of the film of the present invention is not particularly limited, but is preferably 500 μm or less, more preferably 300 μm or less, and particularly preferably 200 μm or less. Further, it is preferably 10 μm or more, more preferably 30 μm or more, further preferably 40 μm or more, and particularly preferably 50 μm or more. If the thickness of the film is within the above range, there is an advantage that it is difficult to be deformed when vacuum forming is performed using the film, and it is difficult to cause breakage at the deep drawing portion, and the optical characteristics are uniform, A film with good transparency can be produced. On the other hand, if the thickness of the film exceeds the above range, cooling of the film after molding becomes non-uniform, and the optical characteristics tend to be non-uniform. Moreover, when the thickness of a film is less than the said range, handling of a film may become difficult.

  The film of this invention can reduce the glossiness of the film surface by a well-known method as needed. For example, it can be carried out by a method of kneading an inorganic filler or crosslinkable polymer particles in a resin composition. Further, the gloss of the film surface can be reduced by embossing the obtained film.

  The film of the present invention can be used for various applications utilizing properties such as heat resistance, transparency, and flexibility. For example, automotive interiors, personal computer interiors, mobile interiors, solar cell interiors, solar cell backsheets; video fields such as cameras, VTRs, projector lenses, viewfinders, filters, prisms, Fresnel lenses, lens covers, Lens field such as optical disk pickup lens for CD player, DVD player, MD player, optical recording field for optical disk such as CD, DVD, MD, organic EL film, light guide plate for liquid crystal, diffusion plate, back sheet, reflection Sheet, polarizer protective film, polarizing film transparent resin sheet, retardation film, light diffusion film, liquid crystal display film such as prism sheet, surface protection film and other information equipment fields, optical fiber, optical switch, optical connector light etc. Communication field, automotive Vehicle field such as drite, tail lamp lens, inner lens, instrument cover, sunroof, etc., medical equipment field such as eyeglasses, contact lens, endoscope lens, medical supplies requiring sterilization, road sign, bathroom equipment, flooring, Road translucent plate, pair glass lens, daylighting window, carport, lighting lens, lighting cover, building material field such as sizing for building materials, microwave cooking container (tableware), housing for home appliances, toys, sunglasses, Can be used for stationery. Moreover, it can be used as an alternative application of a molded product using a transfer foil sheet.

  The film of the present invention can be used by being laminated on a metal, plastic or the like. Film lamination methods include laminate molding, wet laminating after applying an adhesive to a metal plate such as a steel plate, and then drying and pasting the film on the metal plate, dry laminating, extrusion laminating, hot melt laminating, etc. can give.

  As a method of laminating a film on a plastic part, the film is placed in a mold and then placed in a mold after insert molding or laminate injection press molding in which resin is filled by injection molding, or after the film is preformed. In-mold molding in which resin is filled by injection molding can be used.

  As a laminate of the film of the present invention, it can be used as a substitute for painting such as automobile interior materials and automobile exterior materials, window frames, bathroom equipment, wallpaper, flooring materials and other building materials, household goods, furniture and electrical equipment housings. For OA equipment housings such as facsimiles, notebook computers, and copiers, front panels of LCD screens for terminals such as mobile phones, smartphones, and tablets, lighting lenses, automotive headlights, optical lenses, optical fibers, optical disks, and liquid crystal It can be used for optical members such as light guide plates, parts of electrical or electronic devices, medical supplies requiring sterilization, toys or recreational items.

  In particular, the acrylic resin film of the present invention is suitable for an optical film in that it has excellent heat resistance and optical properties, and can be used for various optical members. For example, the front plate of the liquid crystal screen of terminals such as mobile phones, smartphones, tablets, illumination lenses, automobile headlights, optical lenses, optical fibers, optical disks, light guide plates for liquid crystals, diffusion plates, back sheets, reflection sheets, polarizing films Transparent resin sheet, retardation film, light diffusion film, prism sheet, surface protective film, optical isotropic film, polarizer protective film, transparent conductive film, liquid crystal display device periphery, organic EL device periphery, optical communication field etc. It can be applied to known optical applications.

  EXAMPLES Next, although this invention is demonstrated further in detail based on an Example, this invention is not limited only to these Examples. In the following, “part” and “%” mean “part by weight” and “% by weight” unless otherwise specified.

  In addition, each measuring method of the physical property measured in the following Examples and Comparative Examples is as follows.

(Measurement of polymerization conversion)
The obtained latex of the polymer was dried in a hot air dryer at 120 ° C. for 1 hour to determine the solid component amount, and the polymerization conversion rate was calculated by the following formula: (solid component amount / total amount of charged single component) x100
(Measurement of average particle diameter of cross-linked acrylic polymer)
Using the obtained polymer latex diluted to a solid content concentration of 0.02% as a sample, using light scattering at a wavelength of 546 nm using a U-5100 ratio beam spectrophotometer manufactured by Hitachi High-Technologies Corporation. Asked.

(Graft rate)
1 g of the obtained graft copolymer was dissolved in 40 ml of methyl ethyl ketone, and centrifuged for 1 hour at 3000 rpm using a centrifuge (manufactured by Hitachi Koki Co., Ltd., CP60E) to obtain insoluble and soluble components. And separated.

Graft rate (%) = {(weight of insoluble matter of methyl ethyl ketone−weight of monomer constituting the crosslinked polymer / (weight of monomer constituting the crosslinked polymer)} × 100
The weight of the monomer constituting the crosslinked polymer was the monomer component excluding the polyfunctional monomer out of all the monomers. For example, when the crosslinked polymer of the rubber-containing graft copolymer is composed of a methacrylic crosslinked polymer and an acrylic crosslinked polymer, the total amount of the monomer components is used.

(Imidation rate)
The imidation ratio was calculated as follows using IR. The product pellets were dissolved in methylene chloride, and the IR spectrum of the solution was measured at room temperature using a TravelIR manufactured by SensIR Technologies. From the obtained IR spectrum, and the absorption intensity attributable to the ester carbonyl group of 1720cm ^-1 (Absester), the imidization ratio from the ratio of the absorption intensity attributable to the imide carbonyl group of ^{1660cm -1 (Absimide) (Im%} ( IR)). Here, the “imidation rate” refers to the ratio of the imide carbonyl group in the total carbonyl group.

(Content of glutarimide unit)
^{Using 1} H-NMR BRUKER Avance III (400 MHz), ¹ H-NMR measurement of the resin is performed to determine the content (mol%) of each monomer unit such as glutarimide unit or ester unit in the resin, and the content The amount (mol%) was converted to content (% by weight) using the molecular weight of each monomer unit.

(Acid value)
0.3 g of the obtained glutarimide acrylic resin was dissolved in a mixed solvent of 37.5 ml of methylene chloride and 37.5 ml of methanol. After adding 2 drops of phenolphthalein ethanol solution, 5 ml of 0.1N sodium hydroxide aqueous solution was added. Excess base was titrated with 0.1N hydrochloric acid and calculated as the difference in milliequivalents between the base to which the acid value was added and the hydrochloric acid used to reach neutralization.

(Refractive index)
The refractive index of glutarimide acrylic resin was obtained by processing each composition into a sheet and measuring the refractive index (nD) at the sodium D-line wavelength using an Abbe refractometer 2T manufactured by Atago Co., Ltd. according to JIS K7142. .

(Glass-transition temperature)
Using a differential scanning calorimeter (DSC) SSC-5200 manufactured by Seiko Instruments Inc., the sample was once heated to 200 ° C. at a rate of 25 ° C./minute, held for 10 minutes, and then at a rate of 25 ° C./minute to 50 ° C. Measurement is performed while the temperature is raised to 200 ° C. at a rate of temperature increase of 10 ° C./min through preliminary adjustment to lower the temperature, and an integral value is obtained from the obtained DSC curve (DDSC), and the glass transition temperature is determined from the maximum point. Asked.

(Evaluation of transparency)
The transparency of the obtained film was measured by calculating haze at a temperature of 23 ° C. ± 2 ° C. and a humidity of 50% ± 5% according to JIS K6714.

(Static friction coefficient)
A surface property measuring machine (TYPE 14 manufactured by Shinto Kagaku Co., Ltd.) was used. The measurement conditions were a load of 500 g, an FS of 50%, and a friction coefficient between 6 cm long × 5 cm wide films was measured.

(Film elongation)
Measurement was performed at a temperature of 23 ° C. ± 2 ° C. and a humidity of 50% ± 5% according to ISO 527-3.

(Film strength)
Measurement was performed at a temperature of 23 ° C. ± 2 ° C. and a humidity of 50% ± 5% according to ISO 527-3.

(Film appearance)
The obtained film 10 cm long × 10 cm wide was visually observed through transmission from a distance of 20 cm, and judged by the number of defects of 100 μm or more.
A: Less than 50/100 cm 2.
Δ: 50/100 cm 2 or more and less than 100/100 cm 2
X: 100 pieces / 100 cm 2 or more.

Abbreviations represent the following substances.
OSA: sodium dioctylsulfosuccinate BA: n-butyl acrylate MMA: methyl methacrylate tDM: tertiary decyl mercaptan AlMA: allyl methacrylate CHP: cumene hydroperoxide

(Production Example 1) Production of lubricant (A-1) The following substances were charged into a glass reactor.
Ion-exchanged water 125 parts Boric acid 0.47 parts Sodium carbonate 0.05 parts Polyoxyethylene lauryl ether phosphoric acid 0.0042 parts

  After sufficiently replacing the inside of the polymerization apparatus with nitrogen gas, the internal temperature was set to 80 ° C., 25% of (A-1) shown in Table 1 was added to the polymerization apparatus in a lump, and then 5% sodium formaldehyde sulfoxylate was added. -0.00645 parts of ethylenediamine, 0.0056 parts of ethylenediaminetetraacetic acid-2-sodium, and 0.0014 parts of ferrous sulfate, and 15 minutes later, 0.022 parts of t-butyl hydroperoxide was added. Polymerization was continued for 15 minutes. Thereafter, 0.013 part of a 2% aqueous sodium hydroxide solution was added. The remaining 75% was added continuously over 30 minutes. 30 minutes after the completion of the addition, 0.0069 part of 69% t-butyl hydroperoxide was added and held at the same temperature for 30 minutes to complete the polymerization. The polymerization conversion rate was 98%.

(A-2)
The polymer latex obtained in (A-1) was kept at 80 ° C. in a nitrogen stream, and 0.0346 part of sodium hydroxide and 0.0519 part of potassium persulfate were added. Thereafter, a mixture of 32.5 parts of monomer (82% BA, 18% St), 0.97 part AIMA and 0.3 part polyoxyethylene lauryl ether phosphoric acid was continuously added over 74 minutes. Thereafter, it was held for 45 minutes to complete the polymerization.

  The average particle diameter of the obtained polymer was 260 nm, and the polymerization conversion rate was 99%.

(A-3)
(A-2) The obtained rubbery polymer latex was kept at 80 ° C., 0.0097 part of potassium persulfate and 0.05 part of sodium hydroxide were added, and then 50 parts of monomer (MMA 90%, BA 10%). ) Was continuously added over 150 minutes. After completion of the addition of the mixture, it was kept for 1 hour to obtain a latex.

  The average particle size of the lubricant (A-1) was 380 nm, and the polymerization conversion rate was 99%.

  The resulting latex of the lubricant (A-1) was salted out and coagulated with magnesium sulfate, washed with water and dried to obtain a white powdery lubricant (A-1).

(Production Example 2)
<Manufacture of glutarimide acrylic resin>
Using a meshing type unidirectional twin screw extruder, a raw material resin was supplied to a raw material supply port of the first extruder using a constant weight feeder (manufactured by Kubota Corporation).

  The degree of vacuum of each vent in the first extruder and the second extruder was about -0.090 MPa. Furthermore, the pressure control mechanism in the part connects the first extruder and the second extruder with a pipe having a diameter of 38 mm and a length of 2 m, and connects the resin discharge port of the first extruder and the raw material supply port of the second extruder. Used a constant flow pressure valve.

  The resin (strand) discharged from the second extruder was cooled by a cooling conveyor and then cut by a pelletizer to form pellets. Here, in order to determine the pressure in the component connecting the resin discharge port of the first extruder and the raw material supply port of the second extruder, or to determine the extrusion fluctuation, the discharge port of the first extruder, the first extruder and the first extruder Resin pressure gauges were provided at the center of the connecting parts between the two extruders and at the discharge port of the second extruder.

  In the 1st extruder, the polymethyl methacrylate resin (Mw: 105,000) was used as raw material resin, and the imide resin intermediate body 1 was manufactured using monomethylamine as an imidation agent. At this time, the temperature of the highest temperature part of the extruder was 280 ° C., the screw rotation speed was 55 rpm, the raw material resin supply amount was 150 kg / hour, and the addition amount of monomethylamine was 2.0 parts with respect to 100 parts of the raw material resin. The constant flow pressure valve was installed immediately before the raw material supply port of the second extruder, and the monomethylamine press-fitting portion pressure of the first extruder was adjusted to 8 MPa.

  In the second extruder, the imidizing agent and by-products remaining in the rear vent and the vacuum vent were devolatilized, and then dimethyl carbonate was added as an esterifying agent to produce an imide resin intermediate 2. At this time, each barrel temperature of the extruder was 260 ° C., the screw rotation speed was 55 rpm, and the addition amount of dimethyl carbonate was 3.2 parts with respect to 100 parts of the raw resin. Furthermore, after removing the esterifying agent with a vent, it was extruded from a strand die, cooled in a water tank, and then pelletized with a pelletizer to obtain a glutarimide acrylic resin.

  The obtained glutarimide acrylic resin is an acrylic resin obtained by copolymerizing a glutamylimide unit and a (meth) acrylic acid ester unit.

  For the glutarimide acrylic resin, the imidization rate, glutarimide unit content, acid value, glass transition temperature, and refractive index were measured according to the above methods. As a result, the imidation ratio was 13%, the content of glutarimide units was 7% by weight, the acid value was 0.4 mmol / g, the glass transition temperature was 130 ° C., and the refractive index was 1.50.

(Examples 1-3, Comparative Examples 1-3)
The obtained white powdery lubricant (A-1) and acrylic resins (B-1) to (B-3) were blended in proportions (parts) shown in Table 1, respectively, and an antioxidant Irganox 1010 (manufactured by BASF ) 0.4 parts is added, melt kneading is performed by setting the cylinder temperature to 250 ° C. using a single-screw extruder with 40 mmφ vent (Tabata Machine Industries, Ltd., HV-40-28), Pelletized. The obtained pellets were extrusion-molded at a cylinder set temperature of 160 ° C. to 235 ° C. and a die temperature of 250 ° C. using a 40 mmφ extruder with a T-die (manufactured by Nakamura Industries Co., Ltd., NEX04097), and a film having a thickness of 60 μm Got. Various properties described above were evaluated using the obtained film, and the results are shown in Table 2.

Claims (8)

A film comprising a resin composition containing an acrylic resin and a lubricant,
The lubricant is an acrylic crosslinked structure-containing graft copolymer,
The average particle diameter of the (meth) acrylic crosslinked polymer that the acrylic crosslinked structure-containing graft copolymer has is 180 to 400 nm,
The lubricant is contained in 0.1 to 4.5% by weight in 100% by weight of the resin composition,
the film. The acrylic crosslinked structure-containing graft copolymer is
Acrylic acid alkyl ester (a-1) having 1 to 12 carbon atoms in alkyl group (a-1) 60 to 100% by weight, and another monomer unit (a-2) having a double bond copolymerizable therewith Monomer component (a) comprising 40 to 0% by weight, and polyfunctional monomer (a-3) (2.3 to 10 parts by weight with respect to 100 parts by weight of monomer component (a)) Is a graft copolymer having an acrylic cross-linked polymer obtained by polymerizing
The film according to claim 1.   The acrylic crosslinked structure-containing graft copolymer is composed of 60 to 100% by weight of a methacrylic acid ester having an alkyl group having 1 to 4 carbon atoms, and another monomer 40 to 40 having a copolymerizable double bond. The film as described in any one of Claims 1-2 which has a structure where the polymer obtained by superposing | polymerizing the monomer component which consists of 0 weight% has graft-bonded to the said acrylic type crosslinked polymer.   The acrylic cross-linked structure-containing graft copolymer is an alkyl group having 1 to 4 carbon atoms of alkyl methacrylate (c-1) 40 to 100% by weight and other copolymerizable double bonds At least a part of the crosslinked methacrylic polymer obtained by polymerizing the monomer component (c) consisting of 0 to 60% by weight of the monomer and the polyfunctional monomer (c-3). The film as described in any one of Claims 1-3 which is a graft copolymer which has a structure which the type | system | group crosslinked polymer has coat | covered. The acrylic crosslinked structure-containing graft copolymer is
60 to 100% by weight of an alkyl acrylate ester (a-1) having 1 to 12 carbon atoms in the alkyl group, and another monomer (a-2) 40 having a double bond copolymerizable therewith It is obtained by polymerizing a monomer component (a) consisting of ˜0% by weight and a polyfunctional monomer (2.3 to 10 parts by weight with respect to 100 parts by weight of the monomer component (a)). In the presence of an acrylic cross-linked polymer, obtained by polymerizing a monomer mixture containing a methacrylic acid ester having an alkyl group having 1 to 4 carbon atoms,
The film as described in any one of Claims 1-4. The acrylic crosslinked structure-containing graft copolymer particles are
(A-1) A monomer component comprising 40 to 100% by weight of an alkyl methacrylate having 1 to 4 carbon atoms in the alkyl group and 0 to 60% by weight of another monomer copolymerizable therewith. (C) and a polyfunctional monomer (0.01 to 10 parts by weight based on 100 parts by weight of the monomer component (c)) to obtain a methacrylic crosslinked polymer,
(A-2) In the presence of the methacrylic cross-linked polymer, 60 to 100% by weight of an alkyl acrylate ester (a-1) having an alkyl group having 1 to 12 carbon atoms, and copolymerizable therewith The monomer component (a) comprising 40 to 0% by weight of the other monomer (a-2), and a multifunctional monomer (2.3 with respect to 100 parts by weight of the monomer component (a)) To 10 parts by weight) to obtain an acrylic crosslinked polymer,
(A-3) In the presence of the acrylic cross-linked polymer, 60 to 100% by weight of an alkyl group having 1 to 4 carbon atoms in the alkyl group and a double bond copolymerizable therewith Obtained by polymerizing a monomer component (b) comprising 40 to 0% by weight of a monomer,
The film as described in any one of Claims 1-5.   7. The content of the (meth) acrylic crosslinked polymer in 100 wt% of the acrylic crosslinked structure-containing graft copolymer is less than 60 wt% of the acrylic crosslinked structure-containing graft copolymer. The film according to any one of the above. The laminated body by which the film of Claims 1-7 was laminated | stacked on the base material.