JPH1087940A - Resin composition, and lamtnate using the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a resin composition, excellent in extrusion or injection meltability and useful as an adhesive for a polyolefin-based resin to a fluororesin or an acrylic resin. SOLUTION: This resin composition is obtained by compounding (A) 100 pts.wt. acrylic graft copolymer with (B) 1-200 pts.wt. acrylic resin. In this case, the acrylic graft copolymer is obtained by the following method for production: The acrylic graft copolymer A is prepared by reacting (a) an olefinic resin having at least one functional group in one molecule with (b) a radically polymerizable monomer having a functional group having reactivity with the functional group, providing (c) a radically polymerizable olefinic resin and further radically copolymerizing 100 pts.wt. resultant resin (c) with (d) an alkyl acrylate or an alkyl methacrylate (with the proviso that the number of carbon atoms in the alkyl group is 1-8) in an amount of 10-500 pts.wt. based on 100 pts.wt. resin (c).

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an adhesive resin composition comprising an acrylic graft copolymer and an acrylic resin, and a laminate of an olefin resin and a fluororesin obtained by using the same as an adhesive. And a laminate of an olefin resin and an acrylic resin.

[0002]

2. Description of the Related Art Nonpolar olefin resins such as polyethylene and polypropylene are widely used in the fields of household electric appliances, automobile parts, packaging materials and the like because of their advantages such as low cost, light weight, and good moldability. . However, olefin resins do not have sufficient antifouling properties, weather resistance, and chemical resistance to nonpolar solvents.

On the other hand, fluororesins are excellent in antifouling properties, weather resistance, chemical resistance, solvent resistance, and abrasion resistance. However, fluororesins have poor adhesion to various substrates, and have the disadvantage that even when the fluororesins are applied to the surface of various substrates, the formed coating film is easily peeled off. In addition, acrylic resins are widely used as various molded products and acrylic paints because of their excellent weather resistance, design properties, and transparency, and various studies have been made on composites of olefin resins and acrylic resins. However, it is hard to say that the adhesiveness between an olefin resin represented by polyethylene or polypropylene having no polar group and a fluororesin or an acrylic resin is not sufficient, and various methods have been studied to improve this. .

[0004] For example, as a method for improving the adhesion between an olefin resin and a fluororesin, a primer product is obtained by copolymerizing a radical polymerizable olefin resin with an acrylic monomer and / or a fluorine unsaturated monomer. (JP-A-4-20538) and a method of utilizing a composition comprising polyolefin, polyvinylidene fluoride and acryl-grafted polyolefin as an adhesive layer (JP-A-5-295182).
However, these adhesive compositions have insufficient spreadability at the time of melting, and it has been difficult to mold thermoplastic resins by extrusion or injection molding methods generally used.

As a method of improving the adhesiveness with an acrylic resin, a method of utilizing a resin composition comprising an acrylic resin, a polyolefin and an acrylic graft polyolefin as an adhesive between the polyolefin and the acrylic resin (Japanese Patent Application Laid-Open No. 5-295183). However, this composition also has the drawback that the spreadability at the time of melting is not sufficient and the moldability is poor.

[0006]

SUMMARY OF THE INVENTION An object of the present invention is to provide a resin composition having excellent adhesion between an olefin resin and a fluorine resin or an acrylic resin, and excellent melt spreadability during molding. .

[0007]

The present invention provides a resin composition comprising 100 parts by weight of an acrylic graft copolymer (A) and 1 to 200 parts by weight of an acrylic resin (B). An object of the present invention is to provide a resin composition in which the acrylic graft copolymer (A) is a copolymer obtained by the following production method. Acrylic graft copolymer (A): A radical polymerizable monomer (b) having a functional group reactive with the olefin resin (a) having at least one functional group in one molecule. The reaction is carried out to obtain a radically polymerizable olefin resin (c), and alkyl acrylate or alkyl methacrylate (the alkyl group having 1 to 8 carbon atoms) is added to 100 parts by weight of the resin (c).
An acrylic graft copolymer obtained by subjecting (d) to radical copolymerization at a ratio of 10 to 500 parts by weight.

[0008]

DESCRIPTION OF THE PREFERRED EMBODIMENTS Acrylic graft copolymer (A) Olefin resin having at least one functional group in one molecule (a) Olefin resin (a) having at least one functional group in one molecule is It can be obtained by reacting an existing polyolefin with an unsaturated compound having a desired functional group, or copolymerizing various olefins with a desired functional group and an unsaturated compound having an ethylenically unsaturated bond.

In a method of reacting an existing polyolefin with an unsaturated compound having a desired functional group, the precursor polyolefin may be, for example, polyethylene,
Polyα-olefins such as polypropylene, polybutene-1, ethylene-propylene copolymer, ethylene-butene copolymer or copolymers thereof, α-olefins such as ethylene-propylene-diene copolymer, isobutene-isoprene copolymer -Copolymer of olefin and conjugated diene, polybutadiene, polyconjugated diene such as polyisoprene, styrene-butadiene copolymer, styrene-butadiene-styrene block copolymer or hydrogenated product thereof, styrene-isoprene copolymer, styrene A copolymer of an aromatic vinyl compound such as an isoprene-styrene block copolymer, a styrene-butadiene-isoprene-styrene block copolymer, or a hydrogenated product thereof and a conjugated diene, and chlorinated products of these polyolefins.

[0010] Among these polyolefins, styrene elastomers such as polyethylene, polypropylene, chlorinated polyethylene, chlorinated polypropylene, styrene-butadiene-styrene block copolymer and hydrogenated products thereof are preferred. Examples of the functional group introduced into the polyolefin of these precursors include a carboxylic acid or an anhydride thereof, an epoxy group, a hydroxyl group, an isocyanate group, an oxazoline group, and a carbodiimide group. When a carboxylic acid (including an acid anhydride thereof) group is introduced into a polyolefin, preferred unsaturated compounds having such a functional group include (meth) acrylic acid, fumaric acid, maleic acid and its anhydride, and itacone. Unsaturated carboxylic acids such as acids and anhydrides thereof, crotonic acid and anhydrides thereof, citraconic acid and anhydrides thereof, and anhydrides thereof.

When an epoxy group is introduced into the polyolefin, preferred unsaturated compounds include glycidyl (meth) acrylate, 3,4-epoxycyclohexenylmethyl (meth) acrylate, mono- and diglycidyl esters of maleic acid, itacone Unsaturated carboxylic acid glycidyl esters such as mono- and diglycidyl esters of acids, mono- and diglycidyl esters of allylsuccinic acid, glycidyl esters of p-styrenecarboxylic acid, allyl glycidyl ether, 2-methylallyl glycidyl ether, styrene-p-glycidyl Glycidyl ether such as ether, p-glycidylstyrene, 3,4-epoxy-1-butene, 3,4-epoxy-3-methyl-
Epoxy olefins such as 1-butene, vinylcyclohexene monoxide and the like can be mentioned.

Suitable compounds for introducing a hydroxyl group into the polyolefin include hydroxyalkyl (meth) acrylates such as 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate and 2-hydroxybutyl (meth) acrylate. N-methylol (meth) acrylamide, 2-hydroxyethyl acrylate-6-hexanolide addition polymer, alkenyl alcohol such as 2-propen-1-ol, alkynyl alcohol such as 2-propyn-1-ol, hydroxyvinyl ether, and the like. Can be

When an isocyanate group is introduced into the polyolefin, preferable unsaturated compounds include 2-isocyanatoethyl (meth) acrylate, methacryloyl isocyanate, vinyl isocyanate, and isopropenyl isocyanate. When an oxazoline group is introduced into the polyolefin, preferred unsaturated compounds include 2-vinyl-2-oxazoline and 5-methyl-
2-vinyl-2-oxazoline, 4,4-dimethyl-2
-Vinyl-2-oxazoline, 4,4-dimethyl-2-
Vinyl-5,6-dihydro-4H-1,3-oxazine, 4,4,6-trimethyl-2-vinyl-5,6-dihydro-4H-1,3-oxazine, 2-isopropenyl-2-oxazoline , 4,4-dimethyl-2-isopropenyl-2-oxazoline and the like.

When a carbodiimide group is introduced into a polyolefin, preferred unsaturated compounds include methylvinylcarbodiimide, isopropenylmethylcarbodiimide and the like. The reaction between the polyolefin and the unsaturated compound having a functional group is carried out by a conventional method using a radical initiator. Examples of the copolymer obtained by the copolymerization reaction between various olefins and an unsaturated compound having a desired functional group include ethylene- (meth) acrylic acid copolymer,
Ethylene-2-hydroxyethyl (meth) acrylate copolymer, ethylene-glycidyl (meth) acrylate copolymer, ethylene-polyethylene glycol mono (meth) acrylate copolymer, ethylene-vinyl acetate-
(Meth) acrylic acid copolymer, ethylene-ethyl (meth) acrylate- (anhydride) maleic acid copolymer, ethylene-vinyl acetate- (anhydride) maleic acid copolymer, ethylene-vinyl acetate-2-hydroxyethyl ( (Meth) acrylate copolymer, ethylene-vinyl acetate-glycidyl (meth) acrylate copolymer, ethylene-vinyl acetate-polyethylene glycol mono (meth) acrylate copolymer, partially saponified ethylene-vinyl acetate copolymer, and the like. can give.

The copolymerization reaction between various olefins and an unsaturated compound having a desired functional group is carried out by a conventional method using a radical initiator. Among these copolymers, ethylene- (meth) acrylic acid copolymer, ethylene-glycidyl (meth) acrylate copolymer, ethylene-ethyl (meth) acrylate- (anhydride) maleic acid copolymer,
Most preferred is an ethylene-vinyl acetate-glycidyl (meth) acrylate copolymer.

Radical polymerizable monomer (b) Examples of the radical polymerizable monomer having a functional group reactive with the olefin resin (a) having at least one functional group in one molecule include a hydroxyl group, A radical polymerizable monomer having an epoxy group, an isocyanate group, an oxazoline group, and a carbodiimide group is exemplified. Examples of the radical polymerizable monomer having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and 2-hydroxybutyl (meth).
Examples include hydroxyalkyl (meth) acrylates such as acrylates, N-methylolacrylamide, N-methylolmethacrylamide, and hydroxyvinyl ether.

Examples of the radical polymerizable monomer having an epoxy group include glycidyl ethers such as glycidyl (meth) acrylate, allyl glycidyl ether and 2-methylallyl glycidyl ether; 3,4-epoxy-1-butene; Epoxy olefins such as -epoxy-3-methyl-1-butene; mono- and diglycidyl esters of maleic acid; mono- and diglycidyl esters of itaconic acid;

Examples of the radical polymerizable monomer having an isocyanate group include 2-isocyanatoethyl (meth) acrylate, methacryloyl isocyanate, vinyl isocyanate, and isopropenyl isocyanate. Radical polymerizable monomers having an oxazoline group include 2-vinyl-2-oxazoline and 5-methyl-2.
-Vinyl-2-oxazoline, 4,4-dimethyl-2-
Vinyl-2-oxazoline, 4,4-dimethyl-2-vinyl-5,6-dihydro-4H-1,3-oxazine,
4,4,6-trimethyl-2-vinyl-5,6-dihydro-4H-1,3-oxazine, 2-isopropenyl-
2-oxazoline, 4,4-dimethyl-2-isopropenyl-2-oxazoline and the like.

Examples of the radically polymerizable monomer having a carbodiimide group include methyl vinyl carbodiimide, isopropenyl methyl carbodiimide and the like. Among the above monomers, 2-hydroxyethyl (meth) acrylate is a radical polymerizable monomer having a hydroxyl group,
Glycidyl methacrylate is most preferred as the radical polymerizable monomer having an epoxy group, and 2-isocyanatoethyl methacrylate is most preferred as the radical polymerizable monomer having an isocyanate group.

Radical polymerizable olefin resin (c) A radical polymerizable monomer (b) is added to an olefin resin (a) having at least one functional group in one molecule.
The functional group in the radical polymerizable monomer (b) is 0.001 to 10 equivalents, preferably 0.01 to 10 equivalents to 1 equivalent of the functional group.
By adding 5 equivalents, especially 0.05 to 1 equivalent, a radical polymerizable olefin resin (c) having an ethylenically unsaturated bond is obtained. When the amount of the functional group of the radical polymer (b) is less than 0.001 equivalent to the amount of the functional group of (a), the radical polymerizable olefin resin and an acrylic acid alkyl ester or a methacrylic acid alkyl ester (d) described later are used. When copolymerizing (1) and (2), the amount of the homopolymer of the alkyl acrylate or the alkyl methacrylate (d) increases, which is not preferable.

Alkyl acrylate or alkyl methacrylate (d) Examples of the alkyl acrylate or alkyl methacrylate include ester reactants of acrylic acid or methacrylic acid with an aliphatic alcohol having 1 to 8 carbon atoms. . Specific examples include methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, and among them, methyl methacrylate is most preferred. Further, among the above-mentioned alkyl acrylate or alkyl methacrylate (d), 40
Less than weight percent can be replaced by other unsaturated monomers.

Examples of such other copolymerizable monomers include hydroxy (meth) acrylic acid, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate and 2-hydroxybutyl (meth) acrylate. Alkyl (meth) acrylate, diethylaminomethyl (meth) acrylate, dialkylamino (meth) acrylate such as diethylaminoethyl (meth) acrylate, glycidyl methacrylate, (meth) acrylamide, (meth) acrylonitrile, trifluoroethyl (meth) acrylate, Tetrafluoropropyl (meth) acrylate, hexafluorobutyl (meth) acrylate, octafluoropentyl (meth) acrylate, heptadecafluorononyl (meth) acrylate, heptadecuff Orodeshiru (meth) acrylate fluoroalkyl (meth) acrylates such as, tetrafluoroethylene, trifluoroethylene, vinylidene fluoride, vinyl fluoride, monochloro-trifluoroethylene, 1-chloro-2,2-difluoroethylene, 1,1
-Dichloro-2,2-difluoroethylene, vinylidene chlorofluoride, hexafluoropropene, 3,
3,3,2-tetrafluoropropene, trifluoromethylethylene, 2-fluoropropene, 2-chloro-
1,1,3,3,3-pentafluoropropene, 1,
1,2-trichloro-3-trifluoropropene, perfluoro-1-butene, perfluoro-1-heptene,
Perfluoro-1-nonene, 8-H-perfluoro-1
-Octene, perfluorohexylethylene, perfluorooctylethylene, perfluorodecylethylene,
Fluorine-containing unsaturated monomers such as perfluorododecyl ethylene, vinyl acetate, vinyl chloride, ethyl vinyl ether,
Vinyl ethers such as butyl vinyl ether and hexyl vinyl ether; aromatic compounds having a vinyl group such as vinyl ketone, styrene and α-methylstyrene; and olefins such as ethylene, propylene, butene and isoprene.

The acrylic graft copolymer (A) used in the present invention is based on 100 parts by weight of the radically polymerizable olefin resin (c) and the alkyl acrylate or alkyl methacrylate (d) per 100 parts by weight.
To 500 parts by weight, preferably 20 to 300 parts by weight, and most preferably 50 to 300 parts by weight. If the amount of the alkyl acrylate or alkyl methacrylate (d) is less than 10 parts by weight, the adhesive strength with the fluororesin or acrylic resin is insufficient, and if it exceeds 500 parts by weight, the adhesive strength with the polyolefin is insufficient. Become.

This copolymerization reaction comprises toluene, xylene,
Organic solvents such as methyl ethyl ketone, methyl isobutyl ketone, butyl acetate, and cellosolve acetate are used as reaction solvents, and benzoyl peroxide and di-t- peroxide are used as polymerization catalysts.
A peroxide such as butyl or cumene hydroperoxide, an azobis compound such as azobisisobutyronitrile, or the like is used in an amount of 0.1 to 10% by weight, preferably 0.1 to 10% by weight, based on the alkyl acrylate or alkyl methacrylate (d). It can be carried out by using 1 to 5% by weight and heating and reacting at 50 to 200 ° C for 1 to 20 hours. in this case,
The total amount of the radical polymerizable olefin resin (c) and the alkyl acrylate or alkyl methacrylate (d) is 5 to 50% by weight in total in the reaction product.
It is preferable that the amount of the reaction solvent is adjusted so that the reaction is performed, and the reaction is performed in an atmosphere of an inert gas such as a nitrogen gas or in a stream. In order to reduce the residual monomer, an azobis compound and a peroxide may be used in combination as a polymerization initiator. After polymerization, the powder is separated, washed and dried to obtain a powdery acrylic graft copolymer (A).

Acrylic Resin (B) The acrylic resin (B) in the resin composition of the present invention includes (meth) acrylic acid, methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, -Ethylhexyl (meth) acrylate,
Homopolymers such as cyclohexyl (meth) acrylate, glycidyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, (meth) acrylamide, N-methylol (meth) acrylamide, and copolymers thereof are exemplified. Among these, polymethyl (meth) acrylate is most preferred. The molecular weight of the acrylic resin is from 50,000 to 250,000, more preferably from 90,000 to 150,000 in terms of polymerization average molecular weight (in terms of polystyrene). As the acrylic resin (B), a resin containing a filler, a colorant, various stabilizers, a conductive agent, and the like can be used as necessary.

Resin Composition The resin composition of the present invention is obtained by uniformly mixing the acrylic graft copolymer (A) with the acrylic resin (B) by melt mixing. The mixing ratio of the acrylic resin is 1 to 200 parts by weight based on 100 parts by weight of the acrylic graft copolymer (A). If the blending amount of the acrylic resin is too large, it is not preferable because the adhesiveness with the fluororesin or the acrylic resin is insufficient. A more preferred amount of the acrylic resin is 5 to 100 parts by weight, most preferably 10 to 50 parts by weight, based on 100 parts by weight of the acrylic graft copolymer.

The resin composition of the present invention is prepared by preliminarily mixing and blending an acrylic graft copolymer and an acrylic resin from the viewpoint of dispersibility at the time of melt-kneading using an extruder or an injection molding machine. It is preferable to extrude and pelletize. The method of mixing and blending is not particularly limited, and a predetermined amount of two kinds of resins is mixed using a mixing device such as a V blender, a ribbon blender, and a super mixer. Next, the obtained mixture is kneaded with a kneading machine used for ordinary thermoplastic resins, for example, a single-screw or multi-screw kneading extruder, a roll, melt-kneaded using a Banbury mixer, extruded into a strand, and cut or The melt is cooled and pulverized to prepare a resin composition. The temperature during melt-kneading is 120 to 280 ° C, preferably 140 to 260 ° C, and the screw rotation speed is usually 6
It is preferable to granulate at about 0 to 350 rpm. The resin composition of the present invention may contain a filler, a coloring agent, various stabilizers, a conductive agent, and the like, if necessary.

Laminate The laminate of the present invention is obtained by melt-bonding an olefin resin layer and a fluorine resin layer or an olefin resin layer and an acrylic resin layer via the above resin composition. The molding method is not particularly limited, and molding methods generally used for thermoplastic resins, that is, injection molding, hollow molding, extrusion molding, sheet molding, thermoforming,
Molding methods such as rotational molding, lamination molding, and press molding can be applied. Specifically, the following method can be used.

An olefin resin, a resin composition, and
Melt-kneading the fluororesin or acrylic resin individually using separate extruders, feeding this to one multi-layer molding die, merging and laminating in the die, and then co-extruding into a sheet. Hold-type co-extrusion molding method: An olefin resin, a resin composition, and a fluororesin or an acrylic resin are individually melt-kneaded, and they are combined by a flow distribution device and supplied to a co-extrusion die. Feed block type co-extrusion molding method for co-extrusion;

Extrusion lamination method in which a fluororesin or acrylic resin is laminated in a molten state during the extrusion process on a coextruded film of an olefin resin and a resin composition; coextrusion molding of a fluororesin or acrylic resin and a resin composition Extrusion lamination method in which an olefin resin is laminated on a film in a molten state in an extrusion molding process; An olefin resin film is laminated on a molten laminated film in a co-extrusion molding process of a fluororesin or an acrylic resin, and a resin composition. Extrusion lamination method of laminating on a surface; Extrusion lamination method of laminating a fluororesin film or an acrylic resin film on a surface of a resin composition on a molten laminated film in a process of co-extrusion molding of an olefin resin and a resin composition;

An extrusion lamination method in which a coextruded laminated film of an olefin resin and a resin composition is laminated on a molten film of a fluororesin or an acrylic resin in the process of extrusion molding; Extrusion lamination method of laminating a co-extruded laminated film of a fluororesin or acrylic resin and a resin composition; guiding a melted film of the resin composition between an olefin resin and a fluororesin or an acrylic resin, and melt-bonding the film There is a sandwich lamination method for laminating.

The molding temperature at that time is 150 to 260 ° C., preferably 170 to 230 ° C. At the time of molding, an antioxidant, a light stabilizer,
Resin additives such as ultraviolet absorbers, lubricants, and flame retardants can be blended. The thickness of each layer of the laminate obtained by such a method is not particularly limited, and can be determined according to the use. For example, the olefin resin layer is 0.0
05-5 mm, preferably 0.1-3 mm, fluororesin 0.01-5 mm, preferably 0.05-2 mm, resin composition layer 1-500 μm, preferably 10-100
It is about μm.

[0033]

Next, the present invention will be described with reference to examples, but the present invention is not limited to the examples unless it exceeds the gist. Synthesis of Acrylic Graft Copolymer (A) (Synthesis Example 1) 160 kg of toluene in a reactor equipped with a stirrer, a reflux condenser, a dropping funnel and a thermometer, ethylene-maleic anhydride as olefin resin (a)
Ethyl acrylate copolymer (manufactured by Sumitomo Chemical Co., Ltd .:
40 kg of Bondyne LX-4110) and 104 g of hydroquinone monomethyl ether were charged, and the inside of the system was heated to 110 ° C. under an air stream to dissolve it. To this, 1.423 kg of 2-hydroxyethyl acrylate and 1.044 kg of dimethylbenzylamine were added and reacted at the same temperature for 8 hours.

The obtained radical copolymerizable olefin resin was subjected to infrared absorption spectrum analysis. As a result, 32% of the carboxyl groups of the ethylene-maleic anhydride-ethyl acrylate copolymer were esterified with 2-hydroxyethyl acrylate. I was Then, after purging the system with nitrogen,
The temperature was lowered to 80 ° C., 240 kg of toluene, 60 kg of methyl acrylate and 360 g of azobisisobutyronitrile were added, and the reaction was carried out at the same temperature for 2 hours. The operation of further adding 360 g of azobisisobutyronitrile and reacting for 2 hours was repeated four times. This reaction solution was added to 1500 kg of methyl alcohol to precipitate a polymerization product, which was then separated and dried to obtain an acrylic graft copolymer (I-1).

(Synthesis Example 2) Toluene 16 was introduced into a reactor equipped with a stirrer, a reflux condenser, a dropping funnel and a thermometer.
0 kg, 40 kg of an ethylene-glycidyl methacrylate copolymer (trade name: Bondfast 2c, manufactured by Sumitomo Chemical Co., Ltd.) and 104 g of hydroquinone monomethyl ether were charged as the olefin resin (a), and the system was heated to 110 ° C. under an air stream. Dissolved. 0.61 kg of acrylic acid and tetramethylammonium bromide.
After adding 044 kg, the reaction was carried out at the same temperature for 8 hours.

As a result of oxidation measurement of the obtained radical copolymerizable olefin resin solution, 42% of the epoxy groups of the ethylene-glycidyl methacrylate copolymer were esterified with acrylic acid. Subsequently, after the inside of the system was replaced with nitrogen, the temperature was lowered to 80 ° C., and 240 kg of toluene, 60 kg of methyl acrylate, and azobisisobutyronitrile 360
g was added and reacted at the same temperature for 2 hours. The operation of further adding 360 g of azobisisobutyronitrile and reacting for 2 hours was repeated four times. This reaction solution was added to 1500 kg of methyl alcohol to precipitate a polymerization product, which was then separated and dried to obtain an acrylic graft copolymer (I-2).

Example 1 10 kg of the acrylic graft copolymer (I-1) obtained in Synthesis Example 1 and polymethyl methacrylate (trade name: Parapet GF1000, manufactured by Kuraray Co., Ltd .; weight average molecular weight 1) as an acrylic resin
20,000) was mixed for 2 minutes in a blender (Kawata: Supermixer). The mixture was heated at a resin temperature of 14 with a twin-screw extruder (trade name: PCM30φ, manufactured by Ikegai Ironworks Co., Ltd.).
The composition was melt-kneaded under a kneading condition of 0 to 260 ° C. and a screw rotation speed of 250 rpm to obtain a composition, which was extruded into a strand shape from a die, cut and pelletized. Using the pellets of the obtained resin composition, the adhesive strength and the melt spreadability were evaluated by the methods described below. Table 2 shows the results.

<Melting Spreadability> The above pellets were tested at a test temperature of 190 using a Capilloglove 1-B (manufactured by Toyo Seiki Seisaku-sho, Ltd.).
The resin sheet is extruded at a temperature of 10 ° C. and an extrusion speed of 10 mm / min, and the extruded resin sheet is wound into a roll. The take-up speed of the take-up roll was increased, and the take-up speed at which the sheet was broken was measured. <Adhesive strength> Resin composition pellets were prepared by using high-density polyethylene (Mitsubishi Chemical Corporation: Mitsubishi Polyethylene HB330) as an olefin resin and polyvinylidene fluoride (Kureha Chemical Company: KF1000) as a fluororesin.
Also, polymethyl methacrylate (trade name: GF100 manufactured by Kuraray Co., Ltd.) is used as the olefin resin and the acrylic resin.
0), and the adhesive strength was measured by the following method.

The olefin resin (a) and the fluororesin or acrylic resin (c) are melted and kneaded at 210 ° C. by a 50 mmφ extruder, and the resin composition pellets (b) by a 40 mmφ extruder. A three-layer sheet was formed by a so-called feed block method in which the sheets were combined and laminated by a flow velocity distribution device and supplied to a die. As the die, a coat hanger die having a width of 300 mm was used. The obtained three-layer sheet (thickness (a) / (b) / (c) = 0.1 mm / 0.05)
mm / 0.1 mm) was measured for peel strength using an Instron type tensile tester.

Examples 2 to 5 Evaluations were made in the same manner as in Example 1 except that the amount of the acrylic resin was changed as shown in Table 1. Example 6 10 kg of the acrylic graft copolymer (I-2) obtained in Synthesis Example 2 and polymethyl methacrylate (trade name, manufactured by Kuraray Co., Ltd.) as an acrylic resin
Parapet GF1000; abbreviated as PMMA in the table) 5k
g with a blender (Kawata: Super Mixer)
Mix for minutes. The mixture was heated at a resin temperature of 140 to 160 using a twin-screw extruder (trade name: PCM30φ, manufactured by Ikegai Ironworks Co., Ltd.).
The mixture was melt-kneaded under kneading conditions at 250 ° C. and a screw rotation speed of 250 rpm to form a composition, which was then pelletized. Evaluation was performed in the same manner as in Example 1 using the pellets of the obtained resin composition.

Comparative Example 1 Evaluation was made in the same manner as in Example 1 except that no acrylic resin was added. Comparative Example 2 Evaluation was performed in the same manner as in Example 1 except that the amount of the acrylic resin was changed as shown in Table 1. (Comparative Example 3) 1 kg of the acrylic graft copolymer (I-1) obtained in Synthesis Example 1, 4 kg of low-density polyethylene (Mitsubishi Chemical Corp. product name: Mitsubishi Polyethylene LF480M) as an olefin resin, and fluorine Polyvinylidene fluoride (Kureha Chemical Co., Ltd. product name: KF
1000) was mixed in a blender (Kawata: Supermixer) for 2 minutes. The mixture was heated at a resin temperature of 240 using a twin-screw extruder (trade name: PCM30φ, manufactured by Ikegai Ironworks Co., Ltd.).
The mixture was melt-kneaded under a kneading condition of 250 ° C. and a screw rotation speed of 250 rpm to obtain a composition, which was extruded from a die and cut to obtain a pellet. Evaluation was performed in the same manner as in Example 1 using the obtained pellets.

Comparative Example 4 Evaluation was made in the same manner as in Comparative Example 3 except that the amounts of the olefin resin and the fluororesin were changed as shown in Table 1. (Comparative Example 5) 1 kg of the acrylic graft copolymer (I-1) obtained in Synthetic Example 1, 6 kg of low-density polyethylene (Mitsubishi Chemical Corp. product name: Mitsubishi Polyethylene LF480M) as an olefin resin, and acrylic Polymethyl methacrylate (Kuraray Co., Ltd.)
GF1000 was mixed with a blender (Kawata: Supermixer) for 2 minutes. The mixture was heated at a resin temperature of 24 with a twin-screw extruder (trade name: PCM30φ, manufactured by Ikegai Ironworks Co., Ltd.).
The composition was melt-kneaded under kneading conditions of 0 ° C. and a screw rotation speed of 250 rpm to obtain a composition, which was then pelletized. Evaluation was performed in the same manner as in Example 1 using the pellets of the obtained resin composition. (Comparative Examples 6 to 8) Comparative Example 5 except that the amounts of the olefin resin and the acrylic resin were changed as shown in Table 1.
Was evaluated in the same way as Table 2 shows the evaluation results.

[0043]

[Table 1]

[0044]

[Table 2]

[0045]

The resin composition of the present invention has excellent melt moldability and is useful as an adhesive for laminating polyolefin and fluororesin and polyolefin and acrylic resin.

Claims (6)

[Claims] 1. Acrylic graft copolymer (A) 100
A resin composition in which 1 to 200 parts by weight of an acrylic resin (B) is blended in parts by weight, wherein the acrylic graft copolymer (A) is a copolymer obtained by the following method. Composition. Acrylic graft copolymer (A): A radical polymerizable monomer (b) having a functional group reactive with the olefin resin (a) having at least one functional group in one molecule. The reaction is carried out to obtain a radically polymerizable olefin resin (c), and alkyl acrylate or alkyl methacrylate (the alkyl group having 1 to 8 carbon atoms) is added to 100 parts by weight of the resin (c).
An acrylic graft copolymer obtained by subjecting (d) to radical copolymerization at a ratio of 10 to 500 parts by weight. 2. The olefin resin (a) having at least one functional group in one molecule, wherein the functional group is selected from a carboxyl group, an epoxy group, a hydroxyl group, an isocyanate group, an oxazoline group, and a carbodiimide group. The resin composition according to claim 1, which is present. 3. The resin composition according to claim 1, wherein the acrylic resin (B) is a polymethyl methacrylate having a weight average molecular weight of 50,000 to 250,000. 4. A radically polymerizable olefin resin (c)
Is obtained by reacting 2-hydroxyalkyl acrylate (b) with ethylene-maleic anhydride-ethyl acrylate copolymer (a). 5. A radically polymerizable olefin resin (c).
Is obtained by reacting an acrylic acid (b) with an ethylene-glycidyl methacrylate copolymer (a). 6. A laminate in which an olefin resin layer and a fluororesin layer or an acrylic resin layer are bonded via the resin composition according to claim 1.