JP7115289B2 - DECORATION FILM AND METHOD FOR MANUFACTURING DECORATION MOLDED PRODUCT USING IT - Google Patents

Description

The present invention relates to a decorative film to be adhered onto a resin molded article by thermoforming, and a method for producing a decorated molded article using the decorative film. Specifically, it is a decorative film that can suppress wrinkles and breakage of the film during thermoforming and can exhibit sufficient adhesive strength to the resin molded body, and is to be attached to the resin molded body by thermoforming. The present invention relates to a method for manufacturing a decorative molded article using the decorative film. Furthermore, it has excellent thermoformability without uneven contact, good weather resistance and adhesion, suppresses deterioration of weather resistance before and after thermoforming, and has excellent recyclability, and is used for three-dimensional decorative thermoforming. The present invention relates to a decorative film and a method for producing a decorative molded article using the decorative film.

In recent years, demand for decoration techniques to replace painting has increased due to demands for reduction of VOCs (volatile organic compounds), etc., and various decoration techniques have been proposed.

Among them, a technique has been proposed for forming a decorative molded article in which a decorative film and a molded body are integrated by applying a decorative film instead of a coating film to a molded body by vacuum pressure forming or vacuum forming (for example, Patent Document 1 ), which has received particular attention in recent years.

Decoration molding by vacuum pressure molding and vacuum molding has a greater degree of freedom in shape than other decoration molding represented by insert molding. In addition, since it can be thermoformed at a relatively low temperature and low pressure, it is possible to reproduce the texture on the surface of the decorative molded product by adding texture to the surface of the decorative film. It has the advantage of being superior to

In such decorative molding by vacuum pressure forming and vacuum forming, when the decorative film and the molded article are adhered, the decorative film may be broken or wrinkled, or the adhesion between the decorative film and the molded article may occur. There was a problem that sufficient strength could not be obtained. Also, the use of adhesives, tackifiers, etc. has been proposed as a layer for improving the adhesive strength, but they are expensive, the layer structure is extremely complicated, and the solvent resistance and heat resistance are insufficient. , etc.

To solve this problem, a decorative film including an adhesive layer containing a polypropylene resin is applied to a substrate (molded body) made of a polypropylene resin, so that the decorative film and the molded body are heat-sealed. has been proposed (see Patent Documents 2 and 3, for example). The inventions disclosed in Patent Documents 2 and 3 use a polypropylene-based resin as the adhesive layer of the decorative film. It is necessary to provide a layer of resin, polyurethane resin, polycarbonate or the like. By combining different kinds of raw materials in this way, thermoformability such as drawdown property is expressed, and it is possible to ensure thermoformability in a decorative film made of a polypropylene-based resin that does not contain these different kinds of raw materials. The surface of the molded article to which this was adhered was likely to have holes, wrinkles, and entrainment of air, and the membrane was broken, making it impossible to obtain a decorative molded article with excellent appearance. In particular, when polyurethane resin is included as a different raw material, polyurethane resin, which is a thermosetting resin, does not melt when heated, so it is easy to maintain the shape of the film and greatly improves thermoformability, but there is a problem that recyclability is extremely low. rice field.

That is, the decorative films described in Patent Documents 2 and 3 contain different raw materials in order to ensure thermoformability such as adhesiveness and appearance, have a complicated layer structure, and require many steps for their production. Another problem is that it is difficult to recycle decorative films in which different kinds of raw materials are combined.

Japanese Patent Application Laid-Open No. 2002-67137 Japanese Patent Application Laid-Open No. 2013-14027 Japanese Patent Application Laid-Open No. 2014-124940

Hindered amine light stabilizers and UV absorbers are sometimes added to impart weather resistance to the decorative film. However, decorative films containing such hindered amine light stabilizers and UV absorbers have a problem that their weather resistance is significantly impaired after three-dimensional decorative molding.

Conventional technologies have yet to achieve decorative films made from propylene-based resins that are easy to recycle, have both excellent adhesiveness and appearance, and exhibit minimal deterioration in weather resistance even after decorative molding. do not have. In view of the above-mentioned problems, the problem of the present invention is to provide an excellent thermoformability without contact unevenness, good weather resistance and adhesive strength, suppressed deterioration of weather resistance before and after thermoforming, and excellent recyclability. , to provide a decorative film that can be used for three-dimensional decorative thermoforming and a method for producing a decorative molded article using the same.

In three-dimensional decorative thermoforming, it is necessary that the surface of the molded body and the film are sufficiently softened or melted in order to adhere the solid decorative film to the solid resin molded body. Therefore, it is important to apply heat necessary for softening or melting the surface of the molded article and the film, or to use a molded article and film that are easily softened or melted. On the other hand, if the film is heated too much, the viscosity of the film will decrease, and the film will break or run wild due to the push-up of the molded product in the three-dimensional decoration thermoforming process and the inflow of air when returning the vacuum chamber to atmospheric pressure. This leads to poor appearance. The inventors of the present invention focused on the mechanism that causes the above-described poor appearance and, as a result, found that a decorative film containing a layer made of a specific polypropylene-based resin could solve the above-described problems.
Furthermore, it was found that the hindered amine light stabilizer and ultraviolet absorber added to the resin to impart weather resistance volatilized significantly during the process of heating the decorative film under vacuum conditions for the decorative molding. rice field. The present inventors have found that by including a sealing layer with good adhesiveness, it is possible to perform decorative molding at a low temperature in a short period of time, and decorative molding is performed before the hindered amine light stabilizer and ultraviolet absorber volatilize. The inventors have found that the deterioration of weather resistance can be suppressed by completing the process, and have completed the present invention.

That is, the present invention includes the following.

(1) A decorative film containing a hindered amine light stabilizer and/or an ultraviolet absorber for adhering to a resin molding by thermoforming, the decorative film comprising a polypropylene resin (A) and a layer (II) containing a polypropylene-based resin (B), wherein the polypropylene-based resin (A) satisfies the following requirements (a1), and the polypropylene-based resin (B) is the following A decorative film that satisfies requirement (b1).
(a1) Melt flow rate (230° C., 2.16 kg load) (MFR(A)) exceeds 0.5 g/10 minutes.
(b1) Melt flow rate (230° C., 2.16 kg load) (MFR(B)) and MFR(A) satisfy the relational expression (b-1).
MFR(B)<MFR(A) Formula (b-1)

(2) The polypropylene resin (A) further satisfies the following requirements (a2) to (a4), and the polypropylene resin (B) further satisfies the following requirement (b2). decorative film.
(a2) Metallocene-catalyzed propylene polymer.
(a3) The melting peak temperature (Tm(A)) is less than 150°C.
(a4) The molecular weight distribution (Mw/Mn(A)) obtained by GPC measurement is 1.5 to 3.5.
(b2) The melting peak temperature (Tm(B)) and Tm(A) satisfy the relational expression (b-2).
Tm(B)>Tm(A) Formula (b-2)

(3) The addition according to (1) or (2), wherein the polypropylene resin (A) further satisfies the following requirement (a5), and the polypropylene resin (B) further satisfies the following requirement (b3). decorative film.
(a5) The crystallization temperature (Tc(A)) is less than 100°C.
(b3) The crystallization temperature (Tc(B)) and Tc(A) satisfy the relational expression (b-3).
Tc(B)>Tc(A) Formula (b-3)

(4) The seal layer (I) is a resin composition (X3) in which the weight ratio of the polypropylene resin (A) and the ethylene-α-olefin random copolymer (C) is 97:3 to 5:95. The decorative film according to any one of (1) to (3), wherein the ethylene-α-olefin random copolymer (C) satisfies the following requirements (c1) to (c3).
(c1) Ethylene content [E(C)] is 65% by weight or more.
(c2) Density is 0.850 to 0.950 g/cm ³ .
(c3) Melt flow rate (230° C., 2.16 kg load) (MFR(C)) is 0.1 to 100 g/10 minutes.

(5) The sealing layer (I) contains a resin composition (X4) in which the weight ratio of the polypropylene resin (A) and the thermoplastic elastomer (D) is 97:3 to 5:95, and the thermoplastic The decorative film according to any one of (1) to (3), wherein the elastomer (D) satisfies the following requirements (d1) to (d4).
(d1) A thermoplastic elastomer containing at least one of propylene and butene as a main component.
(d2) Density is 0.850-0.950 g/cm ³ .
(d3) Melt flow rate (230° C., 2.16 kg load) (MFR(D)) is 0.1 to 100 g/10 minutes.
(d4) Tensile modulus is smaller than polypropylene resin (A).

(6) The seal layer (I) contains a resin composition (X5) in which the weight ratio of the polypropylene resin (A) and the thermoplastic resin (E) is 97:3 to 5:95, and the thermoplastic The decorative film according to any one of (1) to (3), wherein the resin (E) satisfies the following requirement (e1), and the resin composition (X5) satisfies the following requirement (x1).
(e1) contains at least one of an alicyclic hydrocarbon group and an aromatic hydrocarbon group;
(x1) The isothermal crystallization time (t(X5)) (seconds) of the resin composition (X5) obtained by a differential scanning calorimeter (DSC) satisfies the following formula (x-1).
t(X5)≧1.5×t(A) Expression (x−1)
(In the formula, t (A) represents the isothermal crystallization time (seconds) of the polypropylene resin (A) measured at a temperature 10° C. higher than the crystallization start temperature of the polypropylene resin (A), and t (X5) is It is the isothermal crystallization time (seconds) of the resin composition (X5) measured at a temperature 10°C higher than the crystallization start temperature of the polypropylene resin (A).)

(7) Any one of (1) to (6), wherein the polypropylene resin (A) is a propylene-ethylene block copolymer (F) that satisfies the following requirements (f1) and (f2): decorative film.
(f1) a melting peak temperature (Tm(F)) of 110 to 170°C;
(f2) 5 to 97% by weight of the component (F1) consisting of a propylene homopolymer or a propylene-ethylene random copolymer, and a component (F1) consisting of a propylene-ethylene random copolymer having a higher ethylene content than the component (F1) F2) is contained in an amount of 3 to 95% by weight.

(8) The decorative film according to any one of (1) to (6), wherein the polypropylene resin (A) is a propylene-α-olefin copolymer.

(9) The decorative film according to any one of (2) to (8), wherein the Tm(A) is 140° C. or less.

(10) The ethylene-α-olefin random copolymer (C) further satisfies at least one of the following requirements (c4) and (c5) of (4) and (7) to (9): The decorative film according to any one.
(c4) Melting peak temperature (Tm(C)) is 30 to 130°C.
(c5) A random copolymer of ethylene and an α-olefin having 3 to 20 carbon atoms.

(11) The thermoplastic elastomer (D) is a propylene-ethylene copolymer with an ethylene content of less than 50 wt%, a butene-ethylene copolymer with an ethylene content of less than 50 wt%, or an ethylene content of less than 50 wt%. Any one of (5) and (7) to (9), which is at least one copolymer selected from the group consisting of propylene-ethylene-butene copolymers, propylene-butene copolymers, and butene homopolymers The decorative film described in 1.

(12) The decorative film according to any one of (5), (7) to (9) and (11), wherein the thermoplastic elastomer (D) further satisfies the following requirement (d5).
(d5) The melting peak temperature (Tm(D)) is 30 to 170°C.

(13) The decorative film according to any one of (6) to (9), wherein the thermoplastic resin (E) is a styrene elastomer.

(14) The decorative film according to any one of (6) to (9), wherein the thermoplastic resin (E) is an alicyclic hydrocarbon resin.

(15) Any one of (7) and (9) to (14), wherein the propylene-ethylene block copolymer (F) further satisfies at least one of the following requirements (f3) to (f5): 1. The decorative film according to 1.
(f3) The ethylene content in the propylene-ethylene block copolymer (F) is 0.15 to 85% by weight.
(f4) The ethylene content of component (F1) is in the range of 0 to 6% by weight.
(f5) The ethylene content of component (F2) is in the range of 5 to 90% by weight.

(16) preparing the decorative film according to any one of (1) to (15); preparing a resin molded body; a step of setting a film, a step of reducing the pressure in the chamber box, a step of heating and softening the decorative film, a step of pressing the decorative film against the resin molding, and bringing the pressure in the decompressed chamber box to atmospheric pressure. A method for manufacturing a decorative molded article including a step of returning or pressing.

(17) The method for producing a decorated molded article according to (16), wherein the resin molded article is made of a propylene-based resin composition.

According to the present invention, there is no contact unevenness, excellent thermoformability, good weather resistance and adhesion, suppression of deterioration in weather resistance before and after thermoforming, and excellent recyclability, three-dimensional decorative heat It is possible to provide a decorative film that can be used for molding and a method for producing a decorative molded article using the same.

According to the method for producing the decorated molded article of the present invention, air is not entrained between the decorative film and the resin molded article, and it is possible to obtain a beautifully decorated molded article with good texture reproducibility such as embossing. can. The decorative molded article obtained in this manner does not contain a thermosetting resin layer because the constituent material of the decorative film is a polypropylene-based resin and does not need to contain a thermosetting resin layer. Low deterioration in performance and high recyclability.

1(a) to 1(c) are diagrams showing an example of the layer structure of the decorative film of the present invention. FIG. 2 is a schematic cross-sectional view for explaining the outline of an apparatus used in the method for producing a decorative molded article of the present invention. FIG. 3 is a schematic cross-sectional view for explaining how the resin molding and the decorative film are set in the apparatus of FIG. FIG. 4 is a schematic cross-sectional view illustrating how the inside of the apparatus of FIG. 2 is heated and decompressed. FIG. 5 is a schematic cross-sectional view for explaining how the decorative film is pressed against the resin molding in the apparatus of FIG. FIG. 6 is a schematic cross-sectional view for explaining how the inside of the apparatus of FIG. 2 is returned to atmospheric pressure or pressurized. FIG. 7 is a schematic cross-sectional view for explaining how the edge of the unnecessary decorative film is trimmed in the obtained decorative molded article. 8(a) to 8(c) are diagrams showing an example of the layer structure of the obtained decorative molding.

As used herein, a decorative film refers to a film for decorating a molded article. Decorative molding refers to molding in which a decorative film and a molded body are adhered together. Three-dimensional decorative thermoforming is a process of adhering a decorative film to a molded body, and includes a step of thermoforming the decorative film along the adhering surface of the molded body and simultaneously adhering it, In this step, thermoforming is performed under reduced pressure (vacuum) in order to prevent air from being entrained between the decorative film and the molded article, the heated decorative film is adhered to the molded article, and pressure is applied. It refers to molding, which is the process of bringing into close contact by releasing (pressurizing).

In this specification, each MFR of the polypropylene-based resin and the polypropylene-based resin composition was measured according to ISO 1133:1997 Conditions M under the conditions of 230° C. and 2.16 kg load. The unit is g/10 minutes.

The Mn and Mw of the polypropylene resin are described in "Polymer Chemistry Basics" (Kobunshi Gakkai ed., Tokyo Kagaku Dojin, 1978), etc., and are values calculated from a molecular weight distribution curve by GPC.

Also, in this specification, the unit "wt%" means % by weight.

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, embodiments for carrying out the present invention will be described in detail.

The decorative film of the present invention is a decorative film containing a hindered amine-based light stabilizer and/or an ultraviolet absorber to be adhered onto a resin molding by thermoforming, and the decorative film is a polypropylene-based The sealing layer (I) containing the resin (A) and the layer (II) containing the polypropylene-based resin (B) are included, the polypropylene-based resin (A) satisfies the following requirements (a1), and the polypropylene-based resin ( B) is characterized by satisfying the following requirement (b1).
(a1) Melt flow rate (230° C., 2.16 kg load) (MFR(A)) exceeds 0.5 g/10 minutes.
(b1) Melt flow rate (230° C., 2.16 kg load) (MFR(B)) and MFR(A) satisfy the relational expression (b-1).
MFR(B)<MFR(A) Formula (b-1)

In the first embodiment, the polypropylene resin (A) further satisfies the following requirements (a2) to (a4), and the polypropylene resin (B) further satisfies the following requirement (b2). .
(a2) Metallocene-catalyzed propylene polymer.
(a3) The melting peak temperature (Tm(A)) is less than 150°C.
(a4) The molecular weight distribution (Mw/Mn(A)) obtained by GPC measurement is 1.5 to 3.5.
(b2) The melting peak temperature (Tm(B)) and Tm(A) satisfy the relational expression (b-2).
Tm(B)>Tm(A) Formula (b-2)

In the second embodiment, it is preferable that the polypropylene-based resin (A) further satisfies the following requirement (a5), and the polypropylene-based resin (B) further satisfies the following requirement (b3).
(a5) The crystallization temperature (Tc(A)) is less than 100°C.
(b3) The crystallization temperature (Tc(B)) and Tc(A) satisfy the relational expression (b-3).
Tc(B)>Tc(A) Formula (b-3)

In the third embodiment, the sealing layer (I) is a resin in which the weight ratio of the polypropylene resin (A) and the ethylene-α-olefin random copolymer (C) is 97:3 to 5:95. It is preferable that the ethylene-α-olefin random copolymer (C) including the composition (X3) satisfies the following requirements (c1) to (c3).
(c1) Ethylene content [E(C)] is 65% by weight or more.
(c2) Density is 0.850 to 0.950 g/cm ³ .
(c3) Melt flow rate (230° C., 2.16 kg load) (MFR(C)) is 0.1 to 100 g/10 minutes.

In the fourth embodiment, the sealing layer (I) comprises a resin composition (X4) in which the weight ratio of the polypropylene resin (A) and the thermoplastic elastomer (D) is 97:3 to 5:95. The thermoplastic elastomer (D) preferably satisfies the following requirements (d1) to (d4).
(d1) A thermoplastic elastomer containing at least one of propylene and butene as a main component.
(d2) Density is 0.850-0.950 g/cm ³ .
(d3) Melt flow rate (230° C., 2.16 kg load) (MFR(D)) is 0.1 to 100 g/10 minutes.
(d4) Tensile modulus is smaller than polypropylene resin (A).

In the fifth embodiment, the seal layer (I) comprises a resin composition (X5) in which the weight ratio of the polypropylene resin (A) and the thermoplastic resin (E) is 97:3 to 5:95. Preferably, the thermoplastic resin (E) satisfies the following requirement (e1), and the resin composition (X5) satisfies the following requirement (x1).
(e1) contains at least one of an alicyclic hydrocarbon group and an aromatic hydrocarbon group;
(x1) The isothermal crystallization time (t(X5)) (seconds) of the resin composition (X5) obtained by a differential scanning calorimeter (DSC) satisfies the following formula (x-1).
t(X5)≧1.5×t(A) Expression (x−1)
(In the formula, t (A) represents the isothermal crystallization time (seconds) of the polypropylene resin (A) measured at a temperature 10° C. higher than the crystallization start temperature of the polypropylene resin (A), and t (X5) is It is the isothermal crystallization time (seconds) of the resin composition (X5) measured at a temperature 10°C higher than the crystallization start temperature of the polypropylene resin (A).)

In the sixth embodiment, the polypropylene-based resin (A) is preferably a propylene-ethylene block copolymer (F) that satisfies the following requirements (f1) and (f2).
(f1) a melting peak temperature (Tm(F)) of 110 to 170°C;
(f2) 5 to 97% by weight of the component (F1) consisting of a propylene homopolymer or a propylene-ethylene random copolymer, and a component (F1) consisting of a propylene-ethylene random copolymer having a higher ethylene content than the component (F1) F2) is contained in an amount of 3 to 95% by weight.

[Hindered amine light stabilizer and UV absorber]
In this specification, a hindered amine light stabilizer and an ultraviolet absorber (hereinafter both may be collectively referred to as a "weather resistant agent") are materials that can improve the weather resistance of a resin or the like by being blended into the resin. is.
The weathering agent tends to volatilize under decorative molding conditions, i.e., heating under vacuum. can be completed, and deterioration of weather resistance can be suppressed.

Specific examples of hindered amine light stabilizers used in the present invention include poly{[6-[(1,1,3,3-tetramethylbutyl)amino]-1,3,5-triazine-2, 4-diyl][(2,2,6,6-tetramethyl-4-piperidyl)imino]hexamethylene[(2,2,6,6-tetramethyl-4-piperidyl)imino]}, bis(2,2 ,6,6-tetramethyl-4-piperidyl) sebacate, bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, bis(1,2,2,6,6-pentamethyl-4- piperidyl)-2-butyl-2-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate, N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)hexamethylene diamine, bis(2,2,6,6-tetramethyl-4-piperidyl) di(tridecyl)butane tetracarboxylate, bis(1,2,2,6,6-pentamethyl-4-piperidyl) di( tridecyl)butane tetracarboxylate, 3,9-bis[1,1-dimethyl-2-{tris(2,2,6,6-tetramethyl-4-piperidyloxycarbonyloxy)butylcarbonyloxy}ethyl]-2 ,4,8,10-tetraoxaspiro[5,5]undecane, 3,9-bis[1,1-dimethyl-2-{tris(1,2,2,6,6-pentamethyl-4-piperidyloxy carbonyloxy)butylcarbonyloxy}ethyl]-2,4,8,10-tetraoxaspiro[5,5]undecane, 1,5,8,12-tetrakis[4,6-bis{N-(2,2 ,6,6-tetramethyl-4-piperidyl)butylamino}-1,3,5-triazin-2-yl]-1,5,8,12-tetraazadodecane, 1-(2-hydroxyethyl)- 2,2,6,6-tetramethyl-4-piperidinol/dimethyl succinate condensate, 2-tert-octylamino-4,6-dichloro-s-triazine/N,N'-bis(2,2,6 ,6-tetramethyl-4-piperidyl)hexamethylenediamine condensate, N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)hexamethylenediamine/dibromoethane condensate, 2,2 ,6,6-tetramethyl-4-hydroxypiperidine-N-oxyl, bis(2,2,6,6-tetramethyl-4-oxylpiperidine) sebacate, tetrakis(2,2,6,6-tetramethyl Chill-4-oxylpiperidyl)butane-1,2,3,4-tetracarboxylate, Tetrakis(2,2,6,6-tetramethyl-4-piperidyl)1,2,3,4-butanetetracarboxylate , tetrakis(1,2,2,6,6-pentamethyl-4-piperidyl) 1,2,3,4-butane tetracarboxylate, 3,9-bis(1,1-dimethyl-2-(tris(2 , 2,6,6-tetramethyl-N-oxylpiperidyl-4-oxycarbonyl)butylcarbonyloxy)ethyl)-2,4,8,10-tetraoxaspiro[5,5]undecane and the like. Among these, poly{[6-[(1,1,3,3-tetramethylbutyl)amino]-1,3,5-triazine-2,4diyl][(2,2,6 ,6-tetramethyl-4-piperidyl)imino]hexamethylene [(2,2,6,6-tetramethyl-4-piperidyl)imino]}, 3,9-bis[1,1-dimethyl-2-{ tris(2,2,6,6-tetramethyl-4-piperidyloxycarbonyloxy)butylcarbonyloxy}ethyl]-2,4,8,10-tetraoxaspiro[5,5]undecane, tetrakis(2,2 ,6,6-tetramethyl-4-piperidyl) 1,2,3,4-butane tetracarboxylate.

Examples of commercially available products include LA-68 (registered trademark) and LA-57 (registered trademark) manufactured by ADEKA Corporation, Tinuvin770 (registered trademark), Tinuvin765 (registered trademark) and Chimassorb944 (registered trademark) manufactured by BASF Corporation. and Tinuvin622 (registered trademark).

The hindered amine light stabilizers may be used alone or in appropriate combination of two or more.

The amount of the hindered amine light stabilizer added is preferably in the range of 0.001 to 1.00 parts by weight, more preferably 0.005 to 0.00 parts by weight, per 100 parts by weight of the resin constituting the layer containing the light stabilizer. .50 parts by weight. When the addition amount is within the above range, it is possible to obtain a decorative film and a decorative molded article with good weather resistance.

Specific examples of the ultraviolet absorber used in the present invention include, for example, [2-hydroxy-4-(octyloxy)phenyl](phenyl)methanone, 2-(5-chloro-2H-benzotriazol-2-yl)- 6-tert-butyl-4-methylphenol, 2,2′-methylenebis(4-t-octyl-6-benzotriazolyl)phenol, 2-(4,6-diphenyl-1,3,5-triazine-2- yl)-5-[2-(2-ethylhexanoyloxy)ethoxy]phenol, 2,4,6-tris(2-hydroxy-4-hexyloxy-3-methylphenyl)-1,3,5-triazine, etc. mentioned.

Examples of commercially available products include Adekastab LA-36 (registered trademark), Adekastab 1413 (registered trademark), Adekastab LA-31G (registered trademark), Adekastab LA-46 (registered trademark), Adekastab LA-F70 (registered trademark) manufactured by ADEKA Corporation. registered trademark) and Tinuvin326 (registered trademark) manufactured by BASF Corporation.

The ultraviolet absorbers can be used alone or in an appropriate combination of two or more.

The amount of the ultraviolet absorber to be added is preferably in the range of 0.001 to 1.00 parts by weight, more preferably 0.005 to 0.50, per 100 parts by weight of the resin constituting the layer containing the ultraviolet absorber. weight part. When the addition amount is within the above range, it is possible to obtain a decorative film and a decorative molded article with good weather resistance.

Also, both the hindered amine light stabilizer and the ultraviolet absorber may be contained, in which case the total amount of both weathering agents is 0 per 100 parts by weight of the resin constituting the layer containing the weathering agent. A range of 0.002 to 2.00 parts by weight is preferred, more preferably 0.01 to 1.00 parts by weight.

A higher effect can be exhibited by setting the content ratio of the hindered amine light stabilizer and the ultraviolet absorber within a specific range. The mixing ratio of both weathering agents is preferably 1/5 to 5/1, more preferably 1/4 to 4/1, of hindered amine light stabilizer/ultraviolet absorber. By including both weathering agents, the synergistic effect of the weathering agents makes it possible to obtain a decorative film and a decorated molded article with better weather resistance.

The hindered amine light stabilizer and/or ultraviolet absorber may be contained in all layers of the decorative film, or may be contained only in the surface layer of the decorative film, which is the surface of the decorative molded product. good. In particular, since deterioration due to light progresses from the surface of the molded article, it is more preferable that the surface layer of the decorative film contains a weather resistant agent. For example, in the case of a two-layer decorative film consisting of a sealing layer (I) and a layer (II), it is preferred that the layer (II) contains a hindered amine light stabilizer and/or an ultraviolet absorber. Furthermore, when the surface decorative layer (III), which is an optional layer, is laminated on the layer (II), the surface decorative layer (III) contains a hindered amine light stabilizer and/or an ultraviolet absorber. It preferably contains

[Seal layer (I)]
The decorative film of the present invention includes a sealing layer (I) made of a resin composition (X) containing a polypropylene resin (A). The sealing layer (I) is a layer that comes into contact with the resin molding (substrate) during three-dimensional decorative thermoforming. By providing the sealing layer (I), even if the molding time of the three-dimensional decorative thermoforming is shortened, good adhesion is exhibited, so molding is completed before the weathering agent volatilizes, and deterioration of weather resistance is prevented. can be suppressed.
Hereinafter, the configuration of the sealing layer (I) will be specifically described with reference to the above-described basic embodiment and the first to sixth embodiments.

<Basic embodiment>
In a basic embodiment, the sealing layer (I) contains a polypropylene resin (A). In a basic embodiment, the polypropylene-based resin (A) is preferably a resin that is easily relaxed. By providing the seal layer (I) containing such a polypropylene-based resin (A), good adhesion is exhibited even if the molding time of the three-dimensional decorative thermoforming is shortened, so the weather resistant agent volatilizes. It is possible to complete the molding in advance and suppress deterioration of weather resistance.

<<polypropylene resin (A)>>
1. Melt flow rate (MFR (A)): (a1)
In a basic embodiment, the melt flow rate (230° C., 2.16 kg load) MFR (A) of the polypropylene resin (A) must exceed 0.5 g/10 min, preferably 1 g/10 min. 10 minutes or more, more preferably 2 g/10 minutes or more. Within the above range, relaxation at the time of three-dimensional decorative thermoforming progresses sufficiently, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(A), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

2. Resin Composition The polypropylene-based resin (A) of the basic embodiment can be a resin polymerized by a Ziegler catalyst, a metallocene catalyst, or the like. That is, the polypropylene-based resin (A) can be a Ziegler catalyst-based propylene polymer or a metallocene catalyst-based propylene polymer.

The polypropylene-based resin (A) in the basic embodiment includes various types such as propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer (random polypropylene), propylene block copolymer (block polypropylene), etc. propylene-based polymers, or combinations thereof. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer.

<First Embodiment>
In the first embodiment, the sealing layer (I) is made of a resin composition (X1) containing a polypropylene resin (A). In the first embodiment, the polypropylene-based resin (A) is preferably a resin that is easily melted and relaxed. By providing the seal layer (I) made of the resin composition (X1) containing the polypropylene resin (A), good adhesiveness is exhibited even if the molding time of the three-dimensional decorative thermoforming is shortened. Therefore, it is possible to complete the molding before the weathering agent volatilizes, thereby suppressing deterioration of the weather resistance.

<<polypropylene resin (A)>>
1. Melt flow rate (MFR (A)): (a1)
In the first embodiment, the melt flow rate (230° C., 2.16 kg load) MFR (A) of the polypropylene resin (A) must exceed 0.5 g/10 min, preferably 1 g/10 minutes or more, more preferably 2 g/10 minutes or more. Within the above range, relaxation at the time of three-dimensional decorative thermoforming progresses sufficiently, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(A), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

2. Molecular weight distribution (Mw/Mn (A)): (a4)
Mw/Mn of the polypropylene resin (A) is preferably 1.5-3.5, more preferably 2-3. Within the above range, there are few components with a relatively long relaxation time, and it is easy to relax sufficiently, which is preferable.

3. Melting peak temperature (Tm (A)): (a3)
The melting peak temperature (DSC melting peak temperature, sometimes referred to herein as the "melting point") (Tm (A)) of the polypropylene resin (A) is preferably less than 150°C, more preferably 145° C. or lower, more preferably 140° C. or lower, particularly preferably 130° C. or lower. Sufficient adhesive strength can be exhibited as it is the said range. If the Tm (A) is too low, the heat resistance may be lowered and problems may arise in the use of the molded article.

4. Resin composition: (a2)
The polypropylene-based resin (A) of the first embodiment is preferably a so-called metallocene-catalyzed propylene-based polymer polymerized by a metallocene catalyst. Since the metallocene catalyst has a single active site, the propylene-based polymer polymerized by the metallocene catalyst has a narrow molecular weight distribution and crystallinity distribution, and is easily melted and relaxed. It is possible to fuse with

The polypropylene-based resin (A) in the first embodiment includes various types of propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer (random polypropylene), propylene block copolymer (block polypropylene), and the like. Propylene-based polymers, or combinations thereof can be selected. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer.

The polypropylene-based resin (A) is preferably a propylene-α-olefin copolymer from the viewpoint of adhesiveness. Propylene-α-olefin copolymers generally have a lower melting point than propylene homopolymers and a lower crystallization temperature. Adhesiveness is easy to develop.
As the α-olefin, one or a combination of two or more selected from ethylene and α-olefins having 3 to 8 carbon atoms can be used.

<Second embodiment>
In the second embodiment, the seal layer (I) is made of a resin composition (X2) containing a polypropylene resin (A). In the second embodiment, the polypropylene-based resin (A) is preferably a resin with a slow start of crystallization. By providing the seal layer (I) made of the resin composition (X2) containing the polypropylene-based resin (A), good adhesiveness is exhibited even if the molding time of the three-dimensional decorative thermoforming is shortened. Therefore, it is possible to complete the molding before the weathering agent volatilizes, thereby suppressing deterioration of the weather resistance.

<<polypropylene resin (A)>>
1. Melt flow rate (MFR (A)): (a1)
In the second embodiment, the melt flow rate (230° C., 2.16 kg load) MFR (A) of the polypropylene resin (A) must exceed 0.5 g/10 min, preferably 1 g/10 minutes or more, more preferably 2 g/10 minutes or more. Within the above range, relaxation at the time of three-dimensional decorative thermoforming progresses sufficiently, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(A), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

2. Molecular weight distribution (Mw/Mn (A))
Mw/Mn of the polypropylene resin (A) is preferably 3.5-10, more preferably 3.7-7. Within the above range, surface roughness is less likely to occur during film formation, and the surface appearance is excellent, which is preferable.

3. Crystallization temperature (Tc (A)): (a5)
The crystallization temperature Tc(A) of the polypropylene-based resin (A) is preferably less than 100°C, more preferably 97°C or less, still more preferably 93°C or less. Within the above range, sufficient adhesive strength is exhibited. If Tc(A) is too low, the heat resistance may be lowered and problems may arise in the use of the molded article.

4. Resin composition The polypropylene-based resin (A) of the second embodiment can be a resin polymerized by a Ziegler catalyst, a metallocene catalyst, or the like. That is, the polypropylene-based resin (A) can be a Ziegler catalyst-based propylene polymer or a metallocene catalyst-based propylene polymer.

The polypropylene-based resin (A) in the second embodiment includes various types of propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer (random polypropylene), propylene block copolymer (block polypropylene), and the like. Propylene-based polymers, or combinations thereof can be selected. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer.

The polypropylene-based resin (A) is preferably a propylene-α-olefin copolymer from the viewpoint of adhesiveness. Propylene-α-olefin copolymers usually have a lower crystallization temperature than propylene homopolymers, and are likely to exhibit good adhesiveness even if the molding time for three-dimensional decorative thermoforming is shortened. Molding can be completed before the weathering agent volatilizes, and deterioration of weather resistance can be suppressed.
As the α-olefin, one or a combination of two or more selected from ethylene and α-olefins having 3 to 8 carbon atoms can be used.

<Third embodiment>
In the third embodiment, the seal layer (I) contains a resin composition (X3) containing a polypropylene resin (A) and an ethylene-α-olefin random copolymer (C). By providing the seal layer (I) containing such a resin composition (X3), sufficient adhesive strength is exhibited even if the film heating time during three-dimensional decorative thermoforming is short.

<<polypropylene resin (A)>>
The polypropylene-based resin (A) in the third embodiment includes various types of propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer (random polypropylene), propylene block copolymer (block polypropylene), and the like. Propylene-based polymers, or combinations thereof can be selected. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer.

1. Melt flow rate (MFR (A)): (a1)
The melt flow rate (230° C., 2.16 kg load) MFR (A) of the polypropylene resin (A) contained in the seal layer (I) must exceed 0.5 g/10 min, preferably 1 g /10 minutes or more, more preferably 2 g/10 minutes or more. Within the above range, relaxation at the time of three-dimensional decorative thermoforming progresses sufficiently, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(A), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

2. Melting peak temperature (Tm (A))
The melting peak temperature (Tm(A)) of the polypropylene resin (A) is preferably 110°C or higher, more preferably 115°C or higher, and even more preferably 120°C or higher. Within the above range, the moldability during three-dimensional decorative thermoforming is good. Although the upper limit of the melting peak temperature is not limited, it is preferably 170° C. or less.

3. Resin Composition The polypropylene-based resin (A) in the third embodiment can be a resin polymerized by a Ziegler catalyst, a metallocene catalyst, or the like. That is, the polypropylene-based resin (A) can be a Ziegler catalyst-based propylene polymer or a metallocene catalyst-based propylene polymer.

<<Ethylene-α-olefin random copolymer (C)>>
The ethylene-α-olefin random copolymer (C) used in the seal layer (I) of the third embodiment satisfies the following requirements (c1) to (c3), preferably further requirements (c4) to (c5). have.

1. Ethylene content [E (C)]: (c1)
The ethylene content [E(C)] of the ethylene-α-olefin random copolymer (C) of the third embodiment is preferably 65% by weight or more, more preferably 68% by weight or more, and still more preferably 70% by weight. % by weight or more. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming, and the heating time of the film can be shortened. Although the upper limit of the ethylene content [E(C)] is not particularly limited, it is preferably 95% by weight or less.

(Calculation method of ethylene content [E (C)])
The ethylene content [E(C)] of the ethylene-α-olefin random copolymer (C) can be determined from the integrated intensity obtained by ¹³ C-NMR measurement.

(Calculation method 1 (binary system))
First, a method for calculating the ethylene content [E(C)] in a binary copolymer composed of two types of repeating units will be described. In this case, the ethylene content of the ethylene-α-olefin binary copolymer can be determined by (Formula-1).
Ethylene content (mol%) = IE × 100 / (IE + IX) (Formula-1)
Ethylene content (% by weight) = [ethylene content (mol%) x molecular weight of ethylene] x 100/[ethylene content (mol%) x molecular weight of ethylene + α-olefin content (mol%) x molecular weight of α-olefin]

Here, IE and IX are integral intensities for ethylene and α-olefin, respectively, and can be obtained by the following (formula-2) and (formula-3).
IE=(I _ββ +I _γγ +I _βδ +I _γδ +I _δδ )/2+(I _αγ +I _αδ )/4 (Formula-2)
IX= _Iαα +( _Iαγ + _Iαδ )/2 (Formula-3)
Here, the subscripts of I on the right side represent carbons described in structural formulas (a) to (d) below. For example, αα indicates the methylene carbon based on the α-olefin chain, and I _αα represents the integrated intensity of the signal of the methylene carbon based on the α-olefin chain.

In Structural Formula (d), n represents an odd number of 1 or more.

The integrated intensity used in (Formula-2) and (Formula-3) for each α-olefin of the ethylene-α-olefin binary copolymer will be described below.

<For ethylene-propylene copolymer>
When the α-olefin is propylene, the ethylene content [E(C)] is obtained by substituting the following integrated intensity values into (Formula-2) and (Formula-3).
I _ββ =I _25.0-24.2
I _γγ =I _30.8-30.6
I _βδ = I _27.8-26.8
I _γδ =I _30.6-30.2
I _δδ = I _30.2-28.0
I _αα =I _48.0-43.9
I _αγ +I _αδ =I _39.0-36.2

Here, I indicates integrated intensity, and the numerical value subscripted to I on the right side indicates the range of chemical shift. For example, I _39.0-36.2 indicates the integrated intensity of the ¹³ C signal detected between 39.0 ppm and 36.2 ppm.
The chemical shifts are set to 1.98 ppm for the hexamethyldisiloxane ¹³ C signal and the chemical shifts for the other ¹³ C signals are referenced to this. Similar to ethylene-propylene copolymers, ethylene-1-butene copolymers, ethylene-1-hexene copolymers, and ethylene-1-octene copolymers are also described below.

<For ethylene-1-butene copolymer>
When the α-olefin is 1-butene, the ethylene content [E(C)] is obtained by substituting the following integrated intensity values into (Formula-2) and (Formula-3).
I _ββ =I _24.6-24.4
I _γγ =I _30.9-30.7
I _βδ = I _27.8-26.8
I _γδ =I _30.5-30.2
I _δδ = I _30.2-28.0
I _αα =I _39.3-38.1
I _αγ +I _αδ =I _34.5−33.8

<For ethylene-1-hexene copolymer>
When the α-olefin is 1-hexene, the ethylene content [E(C)] is obtained by substituting the following integrated intensity values into (Formula-2) and (Formula-3).
I _ββ =I _24.5-24.4
I _γγ =I _31.0-30.8
I _βδ = I _27.5-27.0
I _γδ =I _30.6-30.2
I _δδ = I _30.2-28.0
I _αα =I _40.0-39.0
I _αγ +I _αδ =I _35.0-34.0

<For ethylene-1-octene copolymer>
When the α-olefin is 1-octene, the βδ signal and the αγ+αδ signal are superimposed on the methylene carbon of the hexyl branch based on 1-octene (5B6 and 6B6 in the structural formulas below).
I _βδ + I _5B6 = I _27.6-26.7
I _αγ +I _αδ +I _6B6 =I _35.0−34.0

Therefore, I _βδ corrected for overlap of 5B6 and 6B6 and I _αγ +I _αδ are substituted, and the integrated intensity shown below is substituted into (Equation-2) and (Equation-3), and the ethylene content [E (C )].
I _ββ =I _24.7-24.2
I _γγ +I _γδ +I _δδ =I _32.0-28.0
I _βδ = 2/3 x I _27.6-26.7
I _αα =I _40.8-39.6
I _αγ +I _αδ =I _βδ +2×I _ββ

(Calculation method 2 (ternary system))
Next, a method for calculating the ethylene content [E(C)] in a terpolymer composed of three types of repeating units will be described. For example, the ethylene content of an ethylene-propylene-butene terpolymer can be determined by the following (Formula-4).
Ethylene content (mol%) = IE × 100 / (IE + IP + IB) (Formula-4)
Ethylene content (% by weight) = [ethylene content (mol%) x ethylene molecular weight] x 100/[ethylene content (mol%) x ethylene molecular weight + propylene content (mol%) x propylene molecular weight + butene content (mol%) ) x molecular weight of butene]
Here, IE, IP and IB are integrated intensities for ethylene, propylene and butene, respectively, and can be obtained by (Equation-5), (Equation-6) and (Equation-7).
IE=(I _ββ +I _γγ +I _βδ +I _γδ +I _δδ )/2+(I _αγ(P) +I _αδ(P) +I _αγ(B) +I _αδ(B) )/4 (Formula-5)
IP = 1/3 x [I _CH3(P) + I _CH(P) + I _αα(PP) + 1/2 x (I αα _(PB) +I _αγ(P) +I _αδ(P) )] (formula - 6)
IB=1/4×[( _ICH3 (B)+ICH(B ₎ + _I2B2 +Iαα _(BB) )+1/2×(Iαα _(PB) + _Iαγ(B) + _Iαδ(B) )]...・(Formula-7)
Here, the subscript (P) means a signal based on propylene-derived methyl group branching, and similarly (B) means a signal based on butene-derived ethyl group branching.
Also, αα(PP) means a methylene carbon signal based on a propylene linkage, similarly αα(BB) refers to a methylene carbon signal based on a butene linkage, and αα(PB) refers to a methylene carbon signal based on a propylene-butene linkage. means a signal of

Here, the γγ signal overlaps with the tail of the central propylene methine carbon CH(PPE) signal aligned with propylene-propylene-ethylene, making it difficult to separate the γγ signal.
The γγ signal appears in structural formula (c) with two ethylene chains, and the integrated intensity of γγ derived from ethylene and the integrated intensity of βδ in structural formula (c) satisfy (formula-8).
I _βδ (structural formula (c)) = 2 × I _γγ (Formula-8)
Also, βδ appears in the structural formula (d) having three or more ethylene chains, and the integrated intensity of βδ in the structural formula (d) is equal to the integrated intensity of γδ (formula-9).
I _βδ (structural formula (d))=I _γδ (Formula-9)
Therefore, βδ based on Structural Formula (c) and Structural Formula (d) is obtained by (Formula-10).
I _βδ =I _βδ (structural formula (c))+I _βδ (structural formula (d))=2×I _γγ +I _γδ
... (Formula-10)
That is, I _γγ = (I _βδ - I _γδ )/2 (Formula-10′)
Therefore, by substituting (Formula-10') into (Formula-5), IE can be replaced with (Formula-11).
IE=(I _ββ +I _δδ )/2+(I _αγ(P) +I _αδ(P) +I _αγ(B) +I _αδ(B) +3×I _βδ +I _γδ )/4 (Formula-11)
Here, the βδ signal is corrected for the overlap of ethyl branches based on 1-butene, resulting in (Equation-12).
I _βδ = I _{αγ (P)} + I _{α δ (P)} + I _{α γ (B)} + I _{α δ (B)} −2 × I _{β β} (Formula-12)
From (Formula-11) and (Formula-12), IE becomes (Formula-13).
IE=I _δδ /2+I _γδ /4−I _ββ +I _αγ(P) +I _αδ(P) +I _αγ(B) +I _αδ(B) (Formula-13)
Substitute the following into (Formula-13), (Formula-6) and (Formula-7) to obtain the ethylene content.
I _ββ =I _25.2-23.8
I _γδ =I _30.4-30.2
I _δδ = I _30.2-29.8
I _αγ(P) +I _αδ(P) =I _39.5-37.3
I _αγ(B) +I _αδ(B) =I _34.6-33.9
I _CH3(P) = I _22.6-19.0
I _CH(P) = I _29.5-27.6 + I _31.2-30.4 + I _33.4-32.8
I αα _(PP) =I _48.0-45.0
I _CH3(B) = I _11.4-10.0
I _CH(B) = I _35.5-34.7 + I _37.4-36.8 + I _39.7-39.6
Iαα _(BB) =I _40.3-40.0
Iαα _(PB) =I _{44.2-42.0
I2B2} = _I26.7-26.4

For the assignment of each signal, the following five documents were referred to.
Macromolecules, Vol. 10, NO. 4, 1977,
Macromolecules, Vol. 36, No. 11, 2003,
Analytical Chemistry, Vol. 76, No. 19, 2004,
Macromolecules, 2001, 34, 4757-4767,
Macromolecules, Vol. 25, No. 1, 1992.

Even if the α-olefin of the ethylene-α-olefin random copolymer is other than the above, each signal is assigned and the ethylene content can be determined in the same manner as described above.

2. Density: (c2)
The density of the ethylene-α-olefin random copolymer (C) is preferably 0.850 to 0.950 g/cm ³ , more preferably 0.855 to 0.900 g/cm ³ , still more preferably 0 0.860 to 0.890 g/cm ³ . Within the above range, sufficient adhesive strength is exhibited during three-dimensional decorative thermoforming, and film formability is also good.

3. Melt flow rate (MFR (C)): (c3)
The melt flow rate (230° C., 2.16 kg load) (MFR (C)) of the ethylene-α-olefin random copolymer (C) is preferably 0.1 to 100 g/10 min, more preferably 0.5 to 50 g/10 minutes, more preferably 1 to 30 g/10 minutes. Within the above range, good adhesiveness is exhibited even if the molding time for three-dimensional decorative thermoforming is shortened.

4. Melting peak temperature (Tm (C)): (c4)
The melting temperature peak (DSC melting peak temperature) (Tm(C)) of the ethylene-α-olefin random copolymer (C) is preferably 30 to 130°C, more preferably 35 to 120°C, even more preferably. is 40-110°C. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming.

5. Type of ethylene-α-olefin random copolymer (C): (c5)
The ethylene-α-olefin random copolymer (C) is preferably a copolymer of ethylene and an α-olefin having 3 to 20 carbon atoms. Specific examples of α-olefins having 3 to 20 carbon atoms include propylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-heptene, 1-octene and 1-decene. , 1-dodecene, 1-tetradecene, 1-hexadecene, 1-eicosene and the like. Among these, propylene, 1-butene, 1-hexene and 1-octene are particularly preferred.

Such an ethylene-α-olefin random copolymer (C) is produced by copolymerizing each monomer in the presence of a catalyst. Specifically, the ethylene-α-olefin random copolymer (C) is produced by a gas phase method, a solution method, a high pressure method, using a Ziegler catalyst, a Phillips catalyst, a metallocene catalyst, or the like as an olefin polymerization catalyst. can be produced by copolymerizing ethylene with α-olefins such as propylene, 1-butene, 1-hexene, 4-methyl-1-pentene and 1-octene in a process such as slurry method.

Further, the ethylene-α-olefin random copolymer (C) used in the seal layer (I) of the third embodiment can be used singly or in combination of two or more within a range that does not impair the effects of the present invention. can.
Examples of commercially available ethylene-α-olefin random copolymers include the Kernel series manufactured by Japan Polyethylene Co., Ltd., the Toughmer P series and Toughmer A series manufactured by Mitsui Chemicals, Inc., and the Engage EG series manufactured by DuPont Dow. are mentioned.

<<resin composition (X3)>>
In the third embodiment, the resin composition (X3) constituting the seal layer (I) contains a polypropylene resin (A) and an ethylene-α-olefin random copolymer (C) as main components, It may be a mixture or melt-kneaded product of the polypropylene resin (A) and the ethylene-α-olefin random copolymer (C), and the polypropylene resin (A) and the ethylene-α-olefin random copolymer (C ) may be a sequential polymer.

1. Weight ratio of polypropylene resin (A) and ethylene-α-olefin random copolymer (C) The weight ratio ((A):(C)) is preferably selected in the range of 97:3 to 5:95, more preferably 95:5 to 10:90, still more preferably 93:7 to 20: is 80. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming, the heating time of the film can be shortened, and the adhesiveness between the sealing layer (I) and the layer (II) is good. be.

<Fourth Embodiment>
In the fourth embodiment, the seal layer (I) contains a resin composition (X4) containing a polypropylene resin (A) and a thermoplastic elastomer (D) as main components. By providing the seal layer (I) containing such a resin composition (X4), good adhesion is exhibited even if the molding time of three-dimensional decorative thermoforming is shortened, so It is possible to complete the molding immediately and suppress deterioration of weather resistance.

<<polypropylene resin (A)>>
1. Melt flow rate (MFR (A)): (a1)
The melt flow rate (230° C., 2.16 kg load) MFR (A) of the polypropylene resin (A) contained in the seal layer (I) must exceed 0.5 g/10 min, preferably 1 g /10 minutes or more, more preferably 2 g/10 minutes or more. Within the above range, relaxation at the time of three-dimensional decorative thermoforming progresses sufficiently, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(A), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

2. Melting peak temperature (Tm (A))
The melting peak temperature (Tm(A)) of the polypropylene resin (A) is preferably 110°C or higher, more preferably 115°C or higher, and even more preferably 120°C or higher. Within the above range, the moldability during three-dimensional decorative thermoforming is good. Although the upper limit of the melting peak temperature is not limited, it is preferably 170° C. or less.

3. Resin Composition The polypropylene-based resin (A) in the fourth embodiment can be a resin polymerized by a Ziegler catalyst, a metallocene catalyst, or the like. That is, the polypropylene-based resin (A) can be a Ziegler catalyst-based propylene polymer or a metallocene catalyst-based propylene polymer.

The polypropylene-based resin (A) in the fourth embodiment includes various types of propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer (random polypropylene), propylene block copolymer (block polypropylene), and the like. Propylene-based polymers, or combinations thereof can be selected. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer.

<<Thermoplastic elastomer (D)>>
The thermoplastic elastomer (D) used in the sealing layer (I) of the fourth embodiment satisfies the following requirements (d1) to (d4), and preferably further has requirement (d5).

1. Composition: (d1)
The thermoplastic elastomer (D) of the present invention is a thermoplastic elastomer containing at least one of propylene and butene as a main component. Here, the "thermoplastic elastomer containing at least one of propylene and butene as a main component" means (i) a thermoplastic elastomer containing propylene as a main component, (ii) a thermoplastic elastomer containing butene as a main component, (iii) Thermoplastic elastomers containing propylene and butene as main components.

The content of propylene or butene in the thermoplastic elastomer (D) is not particularly limited, but is preferably 30 wt% or more, more preferably 40 wt% or more, still more preferably 50 wt% or more. For example, the thermoplastic elastomer (D) can contain more than 35 wt% propylene or butenes.
Further, the thermoplastic elastomer (D) may contain both propylene and butene, in which case the total component of propylene and butene is the main component of the thermoplastic elastomer (D), and the total content of propylene and butene is It is preferably 30 wt % or more, more preferably 40 wt % or more, and still more preferably 50 wt % or more. When both propylene and butene are included, for example, the thermoplastic elastomer (D) can contain more than 35 wt% of propylene and butene in total. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming, and the heating time of the film can be shortened.

2. Density: (d2)
The thermoplastic elastomer (D) preferably has a density of 0.850 to 0.950 g/cm ³ , more preferably 0.855 to 0.940 g/cm ³ , still more preferably 0.860 to 0.930 g/cm 3 . ^cm3 . Within the above range, sufficient adhesive strength is exhibited during three-dimensional decorative thermoforming, and film moldability is also improved.

3. Melt flow rate (MFR (D)): (d3)
The melt flow rate (230° C., 2.16 kg load) MFR (D) of the thermoplastic elastomer (D) is preferably 0.1 to 100 g/10 min, more preferably 0.5 to 50 g/10 min. , more preferably 1 to 30 g/10 minutes. Within the above range, good adhesiveness is exhibited even if the molding time for three-dimensional decorative thermoforming is shortened.

4. Tensile modulus: (d4)
The tensile modulus of the thermoplastic elastomer (D) is preferably smaller than that of the polypropylene resin (A). More preferably, the thermoplastic elastomer (D) has a tensile modulus of 500 MPa or less, more preferably 450 MPa or less. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming.

5. Melting peak temperature (Tm (D)): (d5)
The melting peak temperature (Tm(D)) of the thermoplastic elastomer (D) is preferably 30 to 170°C, more preferably 35 to 168°C, still more preferably 40 to 165°C or higher. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming.

The thermoplastic elastomer (D) of the present invention can be appropriately selected and used as long as it satisfies the above requirements (d1) to (d4). , a butene-ethylene copolymer with an ethylene content of less than 50 wt%, a propylene-ethylene-butene copolymer, a propylene-butene copolymer, or a butene homopolymer with an ethylene content of less than 50 wt%.

6. Ethylene content [E (D)]
The ethylene content [E(D)] of the propylene-ethylene copolymer, butene-ethylene copolymer or propylene-ethylene-butene copolymer is more preferably 45 wt% or less, still more preferably 40 wt% or less, and is within the above range. When it is, sufficient adhesive strength can be exhibited at the time of three-dimensional decoration thermoforming.

(Calculation method of ethylene content [E (D)])
When the thermoplastic elastomer (D) is an elastomer containing ethylene, the ethylene content [E(D)] of the thermoplastic elastomer (D) can be determined from the integrated intensity obtained by ¹³ C-NMR measurement.
The calculation method is the "calculation method 1 (binary system)" mentioned in the calculation method of the ethylene content [E(C)] of the ethylene-α-olefin random copolymer (C) described in the third embodiment. and “calculation method 2 (ternary system)”.

The thermoplastic elastomer (D) may also be a copolymer of propylene and an α-olefin other than butene as long as it does not impair the effects of the present invention. Specific α-olefins include ethylene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-heptene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1- hexadecene, 1-eicosene and the like. These α-olefins can be used alone or in combination. Among these, 1-hexene and 1-octene are particularly preferred.

The thermoplastic elastomer (D) is produced by copolymerizing each monomer in the presence of a catalyst. Specifically, propylene, 1-butene, And optionally, it can be produced by copolymerizing an α-olefin such as ethylene, 1-hexene, 4-methyl-1-pentene, and 1-octene.

The thermoplastic elastomer (D) selectively used in the sealing layer (I) of the fourth embodiment can be used singly or in combination of two or more as long as the effects of the present invention are not impaired.
Commercially available products of such thermoplastic elastomers include Toughmer XM series, Toughmer BL series and Toughmer PN series manufactured by Mitsui Chemicals, Inc., and VISTAMAXX series manufactured by ExxonMobil Chemical.

<<resin composition (X4)>>
In the fourth embodiment, the resin composition (X4) constituting the seal layer (I) contains a polypropylene resin (A) and a thermoplastic elastomer (D). The resin composition (X4) may be a mixture or melt-kneaded product of the polypropylene resin (A) and the thermoplastic elastomer (D), or the polypropylene resin (A) and the thermoplastic elastomer (D) may be a sequential polymer of

1. Weight ratio of polypropylene resin (A) and thermoplastic elastomer (D) In the resin composition (X4), the weight ratio ((A):(D)) of the polypropylene resin (A) and the thermoplastic elastomer (D) is , 97:3 to 5:95, more preferably 95:5 to 10:90, still more preferably 93:7 to 20:80. Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming, the heating time of the film can be shortened, and the adhesiveness between the seal layer (I) and the layer (II) can be improved. Become.

<Fifth Embodiment>
In the fifth embodiment, the seal layer (I) contains a resin composition (X5) containing a polypropylene resin (A) and a thermoplastic resin (E). By providing the seal layer (I) containing such a resin composition (X5), good adhesiveness is exhibited even if the molding time of three-dimensional decorative thermoforming is shortened, so before the weathering agent volatilizes It is possible to complete the molding immediately and suppress deterioration of weather resistance.

<<polypropylene resin (A)>>
The polypropylene-based resin (A) in the fifth embodiment includes various types of propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer (random polypropylene), propylene block copolymer (block polypropylene), and the like. Propylene-based polymers, or combinations thereof can be selected. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer.

1. Melt flow rate (MFR (A)): (a1)
The melt flow rate (230° C., 2.16 kg load) MFR (A) of the polypropylene resin (A) contained in the seal layer (I) must exceed 0.5 g/10 min, preferably 1 g /10 minutes or more, more preferably 2 g/10 minutes or more. Within the above range, relaxation at the time of three-dimensional decorative thermoforming progresses sufficiently, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(A), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

2. Melting peak temperature (Tm (A))
The melting peak temperature (Tm(A)) of the polypropylene resin (A) is preferably 110°C or higher, more preferably 115°C or higher, and even more preferably 120°C or higher. Within the above range, the moldability during three-dimensional decorative thermoforming is good. Although the upper limit of the melting peak temperature is not limited, it is preferably 170° C. or less.

3. Resin composition The polypropylene-based resin (A) in the fifth embodiment can be a resin polymerized by a Ziegler catalyst, a metallocene catalyst, or the like. That is, the polypropylene-based resin (A) can be a Ziegler catalyst-based propylene polymer or a metallocene catalyst-based propylene polymer.

<<Thermoplastic resin (E)>>
The thermoplastic resin (E) used in the seal layer (I) of the fifth embodiment is a component having a function of delaying the crystallization of the polypropylene resin (A) by being contained in the polypropylene resin (A). . By slowing the crystallization rate of the polypropylene resin (A), the seal layer resin crystallizes (solidifies) before the seal layer (I) and the substrate surface are heat-sealed during decorative molding. It is possible to prevent the adhesive strength from lowering. As a result, even if the decorative film is heated for a short period of time, it exhibits a strong adhesive force. The effect of delaying the crystallization of the polypropylene-based resin (A) was evaluated based on the isothermal crystallization time of the resin composition (X5) described later.

1. Resin composition: (e1)
The thermoplastic resin (E) in the present invention preferably contains at least one of an alicyclic hydrocarbon group and an aromatic hydrocarbon group. Due to the thermoplastic resin (E) having the above characteristics, when mixed with the polypropylene resin (A), the effect of retarding the crystallization of the polypropylene resin (A) is exhibited, and the adhesive strength with the substrate and the substrate It is highly effective in making scratches on the surface less noticeable. Specifically, the alicyclic hydrocarbon group includes a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cyclooctyl group, and substituent derivatives thereof, condensed cyclized products, crosslinked structures, and the like. It is particularly preferable to contain a cyclopentyl group or a cyclohexyl group. Examples of the aromatic hydrocarbon group include phenyl group, methylphenyl group, biphenyl group, indenyl group, fluorenyl group, and substituent derivatives and condensed cyclized products thereof. preferably. Also, the alicyclic hydrocarbon group may be obtained by hydrogenating an aromatic hydrocarbon group contained in the resin.

The thermoplastic resin (E) can be appropriately selected and used as long as it satisfies the above requirement (e1), but a styrene elastomer or an alicyclic hydrocarbon resin is particularly preferably used. Yes, both may be included.

Styrene-based elastomers include styrene/butadiene/styrene triblock copolymer elastomer (SBS), styrene/isoprene/styrene triblock copolymer elastomer (SIS), styrene-ethylene/butylene copolymer elastomer (SEB), styrene - ethylene-propylene copolymer elastomer (SEP), styrene-ethylene-butylene-styrene copolymer elastomer (SEBS), styrene-ethylene-butylene-ethylene copolymer elastomer (SEBC), hydrogenated styrene-butadiene elastomer (HSBR) ), styrene-ethylene/propylene-styrene copolymer elastomer (SEPS), styrene-ethylene/ethylene/propylene-styrene copolymer elastomer (SEEPS), styrene-butadiene/butylene-styrene copolymer elastomer (SBBS), etc. For example, a hydrogenated one can be particularly preferably used.
Commercially available products include the Dynalon series manufactured by JSR Corporation, the Kraton G series manufactured by Kraton Polymer Japan, and the Tuftec series manufactured by Asahi Kasei Corporation.

Examples of the alicyclic hydrocarbon resin include hydrocarbons obtained by polymerizing one or a mixture of two or more dicyclopentadiene derivatives such as dicyclopentadiene, methyldicyclopentadiene, and dimethyldicyclopentadiene as a main raw material. resins, hydrogenated coumarone-indene resins, hydrogenated C9 petroleum resins, hydrogenated C5 petroleum resins, C5/C9 copolymer petroleum resins, hydrogenated terpene resins, hydrogenated rosin resins, etc., and commercially available Products can be used, and specific examples include the Alcon series manufactured by Arakawa Chemical Co., Ltd., and the like.

<<resin composition (X5)>>
In the fifth embodiment, the resin composition (X5) constituting the sealing layer (I) contains a polypropylene resin (A) and a thermoplastic resin (E) as main components, and the polypropylene resin (A) and the thermoplastic resin (E), or may be a melt-kneaded product.

1. Weight ratio of polypropylene resin (A) and thermoplastic resin (E) In the resin composition (X5), the weight ratio ((A):(E)) of the polypropylene resin (A) and the thermoplastic resin (E) is , 97:3 to 5:95, more preferably 95:5 to 10:90, still more preferably 93:7 to 20:80. Here, a plurality of types of polypropylene resin (A) or thermoplastic resin (E) may be contained, for example, when thermoplastic resin (E1) and thermoplastic resin (E2) are contained, thermoplastic resin ( The sum of E1) and the thermoplastic resin (E2) is taken as the weight of the thermoplastic resin (E). Within the above range, sufficient adhesive strength can be exhibited during three-dimensional decorative thermoforming, and the heating time of the film can be shortened. Furthermore, the adhesion between the sealing layer (I) and the layer (II) is good.

2. Isothermal crystallization time (t(X5)): (x1)
The resin composition (X5) has an isothermal crystallization time (t (X5)) (seconds) determined by a differential thermal scanning calorimeter (DSC) according to the following formula (x-1) is preferably satisfied, more preferably formula (x-2), and even more preferably (x-3).
t(X5)≧1.5×t(A) Expression (x−1)
t(X5)≧2.0×t(A) Expression (x−2)
t(X5)≧2.5×t(A) Expression (x−3)
(In the formula, t (A) represents the isothermal crystallization time (seconds) of the polypropylene resin (A) measured at a temperature 10° C. higher than the crystallization start temperature of the polypropylene resin (A), and t (X5) is It is the isothermal crystallization time (seconds) of the resin composition (X5) measured at a temperature 10°C higher than the crystallization start temperature of the polypropylene resin (A).)
When the isothermal crystallization time (t(X5)) of the resin composition (X5) is within the above range, the seal layer (I) of the decorative film and the substrate surface are heat-sealed during decorative molding. time can be obtained, and high adhesive strength is exhibited.
The upper limit of the isothermal crystallization time (t(X5)) is not particularly limited, but when 30t(A)≧t(X5), the formability of the film is good.

(Measurement of isothermal crystallization time by differential scanning calorimeter (DSC))
The isothermal crystallization time in the present invention is a value measured using a differential scanning calorimeter (DSC) and conforms to JIS-K7121 (2012) "Method for measuring transition temperature of plastics".

Specifically, 5 mg of a sample of polypropylene resin (A) is placed in an aluminum holder and heated from 40° C. to 200° C. at a rate of 10° C./min under a nitrogen atmosphere. After holding at 200° C. for 10 minutes, crystallization is performed to 40° C. at a cooling rate of 10° C./min, and the crystallization start temperature is measured and calculated from the DSC curve at this time.

Next, 5 mg of a sample of polypropylene resin (A) or resin composition (X5) was placed in an aluminum holder and heated from 40° C. to 200° C. at a rate of 10° C./min under a nitrogen atmosphere and held for 10 minutes. Thaw the sample. Subsequently, it is cooled at a rate of 40° C./min to a temperature 10° C. higher than the crystallization start temperature of the polypropylene resin (A) obtained by the method described above (hereinafter sometimes referred to as “measurement temperature”), and then measured. The temperature is maintained and the behavior of the sample to crystallize and exotherm is measured. The isothermal crystallization time is defined as the time from when the temperature of the sample reaches the measurement temperature to when the exothermic peak occurs. Here, since it is conceivable that even a slight crystallization of the sealing layer (I) of the decorative film during decorative molding causes a large decrease in adhesive strength, there are two or more exothermic peaks in the isothermal crystallization measurement. In this case, the isothermal crystallization time is the time until the first exothermic peak.
In addition, depending on the type of polypropylene resin (A), the isothermal crystallization time of polypropylene resin (A) is extremely short (e.g., 120 seconds or less) or long even when measured at a temperature 10°C higher than the crystallization start temperature. (for example, 3000 seconds or more) may occur. In that case, the isothermal crystallization time may be measured at a temperature 10±2° C. higher than the crystallization start temperature. However, when such a measurement is performed, the isothermal crystallization time of the resin composition (X5) must also be measured according to the measurement temperature of the polypropylene resin (A).

<Sixth embodiment>
In the sixth embodiment, a resin composition (X6) containing a propylene-ethylene block copolymer (F) is used as the polypropylene-based resin (A) of the sealing layer (I). By providing such a sealing layer (I), even if the molding time of three-dimensional decorative thermoforming is shortened, good adhesion is exhibited, so molding is completed before the weathering agent volatilizes, and weather resistance is improved. It is possible to suppress the decrease in

<<Propylene-ethylene block copolymer (F)>>
The propylene-ethylene block copolymer (F) used in the sixth embodiment contains a component (F1) consisting of a propylene homopolymer or a propylene-ethylene random copolymer and more ethylene than the component (F1). It contains a component (F2) consisting of a propylene-ethylene random copolymer. The component (F2), which is a rubber component in the propylene-ethylene block copolymer (F), improves the adhesive strength to the resin molding (substrate). The propylene-ethylene block copolymer (F) is obtained by (co)polymerizing the component (F1) consisting of propylene alone or a propylene-ethylene random copolymer in the first polymerization step, and then the component (F1) in the second polymerization step. obtained by successive copolymerization of the component (F2) comprising a propylene-ethylene random copolymer containing a large amount of ethylene.

1. Ratio of component (F1) and component (F2): (f2)
The compounding ratio of the component (F1) and the component (F2) constituting the propylene-ethylene block copolymer (F) in the sixth embodiment is 5 to 97% by weight of the component (F1) and 3 to 97% by weight of the component (F2). 95% by weight is preferred. More preferably, component (F1) is 30 to 95% by weight and component (F2) is 5 to 70% by weight, and more preferably component (F1) is 52 to 92% by weight and component (F2) is 8 to 48% by weight. When the ratio of component (F1) and component (F2) is within the above range, sufficient adhesive strength can be exhibited. Further, within the above range, the film is not sticky and the film formability is good.

2. Melt flow rate (MFR (F)): (a1)
The melt flow rate (230° C., 2.16 kg load) MFR (F) of the propylene-ethylene block copolymer (F) must exceed 0.5 g/10 min, preferably 1 g/10 min or more. , more preferably 2 g/10 minutes or more. When the MFR (F) is within the above range, relaxation of the propylene-ethylene block copolymer (F) proceeds sufficiently during three-dimensional decorative thermoforming, and sufficient adhesive strength can be exhibited. Although there is no upper limit for MFR(F), it is preferably 100 g/10 minutes or less. Within the above range, deterioration in adhesive strength due to deterioration in physical properties does not occur.

3. Melting peak temperature (Tm (F)): (f1)
The melting point (melting peak temperature) Tm(F) of the propylene-ethylene block copolymer (F) is preferably 110 to 170°C. It is more preferably 113 to 169°C, still more preferably 115 to 168°C. When Tm(F) is within the above range, moldability during three-dimensional decorative thermoforming is good. The peak melting temperature is mainly derived from the component (F1) with a low ethylene content, that is, the component (F1) with high crystallinity, and the peak melting temperature can be changed depending on the content of ethylene to be copolymerized.

4. Propylene-ethylene content in ethylene block copolymer (F) (E (F)): (f3)
The ethylene content in the propylene-ethylene block copolymer (F) (hereinafter referred to as "E(F)") is preferably 0.15 to 85% by weight. More preferably 0.5 to 75% by weight, still more preferably 2 to 50% by weight. When E(F) is within the above range, a sufficient adhesive strength can be exhibited, and the adhesiveness to the layer (II) of the decorative film is good, resulting in excellent film moldability.

5. Ethylene content of component (F1) (E (F1)): (f4)
Component (F1) is a propylene homopolymer or propylene-ethylene random copolymer having a relatively high melting point and an ethylene content (hereinafter referred to as "E(F1)") in the range of 0 to 6% by weight. is preferred. More preferably 0 to 5% by weight. When E(F1) is within the above range, the moldability during three-dimensional decoration thermoforming is good, and the film is less sticky and excellent in film moldability.

6. Ethylene content of component (F2) (E(F2)): (f5)
The ethylene content of component (F2) (hereinafter referred to as "E(F2)") is higher than the ethylene content E(F1) of component (F1). Further, it is preferably a propylene-ethylene random copolymer in which E(F2) is in the range of 5 to 90% by weight. E(F2) is more preferably 7 to 80% by weight, more preferably 9 to 50% by weight. Sufficient adhesive strength can be exhibited as E(F2) is within the above range.

(Method for producing propylene-ethylene block copolymer (F))
The propylene-ethylene block copolymer (F) used in the present invention, the component (F1) comprising a propylene homopolymer or a propylene-ethylene random copolymer constituting it, and the component (F2) comprising a propylene-ethylene random copolymer ) can be preferably produced by the following raw materials and polymerization method. A method for producing the propylene-ethylene block copolymer (F) used in the present invention is described below.

・Materials used The catalysts used in the production of the propylene-ethylene block copolymer (F) used in the present invention include magnesium, halogen, titanium, a magnesium-supported catalyst containing an electron donor as a catalyst component, and trichloride. A catalyst consisting of a titanium-catalyzed solid catalyst component and an organoaluminum, or a metallocene catalyst can be used. Specific catalyst production methods are not particularly limited, but examples include the Ziegler catalyst disclosed in Japanese Patent Application Laid-Open No. 2007-254671 and the metallocene catalyst disclosed in Japanese Patent Application Laid-Open No. 2010-105197. can be exemplified.

The raw material olefins to be polymerized are propylene and ethylene, and if necessary, other olefins such as 1-butene, 1-hexene, 1-octene, 4-methyl-1 - It is also possible to use pentene or the like.

-Polymerization step The polymerization step performed in the presence of the catalyst consists of multiple stages of a first polymerization step for producing the component (F1) and a second polymerization step for producing the component (F2).

First polymerization step In the first polymerization step, propylene alone or a propylene/ethylene mixture is supplied to a polymerization system to which the catalyst is added to produce a propylene homopolymer or a propylene-ethylene random copolymer. In this step, component (F1) is formed in an amount corresponding to 5 to 97% by weight of the combined amount.

The MFR of component (F1) (hereinafter referred to as "MFR (F1)") can be adjusted by using hydrogen as a chain transfer agent. Specifically, increasing the concentration of hydrogen, which is a chain transfer agent, increases the MFR (F1) of the component (F1). The reverse is also true. In order to increase the concentration of hydrogen in the polymerization tank, the amount of hydrogen supplied to the polymerization tank can be increased, and adjustment is extremely easy for those skilled in the art. Further, when the component (F1) is a propylene-ethylene random copolymer, it is convenient to use a method of controlling the amount of ethylene supplied to the polymerization reactor as means for controlling the ethylene content. Specifically, the ethylene content of the component (F1) is increased by increasing the ratio of ethylene to propylene supplied to the polymerization reactor (ethylene supply amount/propylene supply amount). The same is true vice versa. The relationship between the amount ratio of propylene and ethylene supplied to the polymerization reactor and the ethylene content of the component (F1) varies depending on the type of catalyst used, but the component having the desired ethylene content can be obtained by appropriately adjusting the supply amount ratio. Obtaining (F1) is quite straightforward for those skilled in the art.

Second polymerization step In the second polymerization step, following the first polymerization step, a propylene/ethylene mixture is further introduced to produce a propylene-ethylene random copolymer, and the amount of the total polymer is 3 to 95% by weight. It is a step of forming the component (F2) so as to have a corresponding amount.

The MFR of component (F2) (hereinafter referred to as "MFR (F2)") can be adjusted by using hydrogen as a chain transfer agent. A specific control method is the same as the control method for the MFR of the component (F1). As a means for controlling the ethylene content of component (F2), it is convenient to use a method of controlling the amount of ethylene supplied to the polymerization tank. A specific control method is the same as when the component (F1) is a propylene-ethylene random copolymer.

Next, a method for controlling the index of the propylene-ethylene block copolymer (F) will be described.
First, a method for controlling the weight ratio of component (F1) and component (F2) will be described. The weight ratio of component (F1) to component (F2) is controlled by the production amount in the first polymerization step for producing component (F1) and the production amount in the second polymerization step for producing component (F2). For example, in order to increase the amount of component (F1) and decrease the amount of component (F2), the production amount in the second polymerization step may be reduced while maintaining the production amount in the first polymerization step. The residence time in the polymerization step may be shortened or the polymerization temperature may be lowered. Moreover, it can be controlled by adding a polymerization inhibitor such as ethanol or oxygen, or by increasing the amount of addition if it is originally added. The opposite is also true.

Usually, the weight ratio of component (F1) to component (F2) is defined by the production amount in the first polymerization step for producing component (F1) and the production amount in the second polymerization step for producing component (F2). The formula is shown below.
Weight of component (F1): weight of component (F2) = W(F1): W(F2)
W (F1) = production amount in the first polymerization step / (production amount in the first polymerization step + production amount in the second polymerization step) x 100
W (F2) = production amount in the second polymerization step / (production amount in the first polymerization step + production amount in the second polymerization step) x 100
W(F1)+W(F2)=100
(Here, W(F1) and W(F2) are the weight ratios (percentages) of the component (F1) and the component (F2) in the propylene-ethylene block copolymer (F), respectively.)

In industrial manufacturing facilities, it is common to obtain the production amount from the heat balance and material balance of each polymerization tank. Further, when the crystallinity of the component (F1) and the component (F2) are sufficiently different, the two may be separated and identified using an analysis method such as TREF (temperature rising elution fractionation method) and the quantitative ratio may be obtained. Techniques for evaluating the crystallinity distribution of polypropylene by TREF measurement are well known to those skilled in the art. Glokner, J.; Appl. Polym. Sci: Appl. Poly. Symp. 45, 1-24 (1990); Wild, Adv. Polym. Sci. 98, 1-47 (1990), J. Am. B. P. Soares, A.; E. Hamielec, Polyer; 36, 8, 1639-1654 (1995) and other literatures show detailed measurement methods.

Next, a method for controlling the ethylene content will be described. Propylene-ethylene block copolymer (F) is a mixture of component (F1) consisting of propylene homopolymer or propylene-ethylene random copolymer and component (F2) consisting of propylene-ethylene random copolymer. The following relational expression holds between the ethylene contents of
E(F)=E(F1)×W(F1)/100+E(F2)×W(F2)/100
(Here, E (F), E (F1) and E (F2) are the component (F1) consisting of a propylene-ethylene block copolymer (F), a propylene homopolymer or a propylene-ethylene random copolymer, respectively. , and the ethylene content of the component (F2) consisting of a propylene-ethylene random copolymer, and W (F1) and W (F2) are the same as above.)

This formula shows the material balance with respect to ethylene content.
Therefore, if the weight ratio of component (F1) and component (F2) is determined, that is, if W(F1) and W(F2) are determined, E(F) is uniquely defined by E(F1) and E(F2). Determined by In other words, E(F) can be controlled by controlling the weight ratio of component (F1) and component (F2), and the three factors E(F1) and E(F2). For example, to increase E(F), E(F1) may be increased, or E(F2) may be increased. Also, keeping in mind that E(F2) is higher than E(F1), it can be easily understood that W(F1) may be decreased and W(F2) increased. The control method in the reverse direction is also the same.

It should be noted that it is E(F) and E(F1) that can actually obtain the measured values directly, and E(F2) is calculated using the measured values of both. Therefore, if an operation to increase E (F) is performed, if an operation to increase E (F2), that is, an operation to increase the amount of ethylene supplied to the second polymerization step is selected as a means, the measured value is directly What can be confirmed is E(F), not E(F2), but it is obvious that the reason for the increase in E(F) is the increase in E(F2).

Finally, a method for controlling MFR(F) will be described. In the present application, MFR(F2) is defined by the following formula.
MFR(F2)=exp{(loge[MFR(F)]−(W(F1)/100)×
loge[MFR(F1)])÷(W(F2)/100)}
(Here, log is the logarithm to the base e. MFR (F), MFR (F1) and MFR (F2) are respectively propylene-ethylene block copolymer (F), propylene homopolymer or propylene- MFR of the component (F1) consisting of an ethylene random copolymer and the component (F2) consisting of a propylene-ethylene random copolymer, where W (F1) and W (F2) are the same as above.)

This formula is an empirical formula generally called logarithmic addition rule of viscosity log [MFR (F)] = (W (F1) / 100) × log [MFR (F1)] + (W (F2) / 100) × log [ MFR(F2)]
and is routinely used in the industry.

Due to the definition in this formula, the weight ratios of component (F1) to component (F2), MFR(F), MFR(F1) and MFR(F2) are not independent. Therefore, in order to control MFR(F), the weight ratio of component (F1) and component (F2), MFR(F1) and MFR(F2) should be controlled. For example, in order to increase MFR(F), MFR(F1) may be increased, or MFR(F2) may be increased. Also, it can be easily understood that when MFR(F2) is lower than MFR(F1), MFR(F) can be increased by increasing W(F1) and decreasing W(F2). . The control method in the reverse direction is also the same.

It is to be noted that MFR(F) and MFR(F1) can actually be obtained directly, and MFR(F2) is calculated using both measured values. Therefore, if an operation to increase the MFR (F) is performed, if an operation to increase the MFR (F2), that is, an operation to increase the amount of hydrogen supplied to the second polymerization step is selected as a means, the measured value is directly What can be confirmed is MFR(F), not MFR(F2), but it is obvious that the cause of the increase in MFR(F) is the increase in MFR(F2).

The propylene-ethylene block copolymer polymerization process can be carried out by either a batchwise method or a continuous method. At this time, a method of conducting polymerization in an inert hydrocarbon solvent such as hexane, heptane, etc., a method of using propylene as a solvent without substantially using an inert solvent, a method of using a gaseous solvent without substantially using a liquid solvent. A method of polymerizing in a monomer and a method of combining these methods can be employed. Moreover, the same polymerization tank may be used for the first polymerization step and the second polymerization step, or separate polymerization tanks may be used.

(1) Measurement of Ethylene Content in Copolymer Using the propylene-ethylene block copolymer (F), each ethylene content in this copolymer was measured. That is, the component (F1) composed of the propylene homopolymer or propylene-ethylene random copolymer obtained at the end of the first polymerization step, and the propylene-ethylene block copolymer (F) obtained through the second polymerization step. Each ethylene content in was obtained by analyzing the ¹³ C-NMR spectrum measured according to the following conditions by the proton complete decoupling method.
Model: GSX-400 manufactured by JEOL Ltd. or equivalent device (carbon nuclear resonance frequency of 100 MHz or higher)
Solvent: o-dichlorobenzene + deuterated benzene (4:1 (volume ratio))
Concentration: 100 mg/mL
Temperature: 130°C
Pulse angle: 90°
Pulse interval: 15 seconds Accumulation times: 5,000 times or more Spectral attribution may be performed, for example, with reference to Macromolecules 17, 1950 (1984). The attribution of the spectrum measured under the above conditions is as shown in the table below. Symbols such as Sαα in the table follow the notation of Carman et al. (Macromolecules 10, 536 (1977)), P represents methyl carbon, S represents methylene carbon, and T represents methine carbon.

Hereinafter, when "P" is the propylene unit in the copolymer chain and "E" is the ethylene unit, six types of triads of PPP, PPE, EPE, PEP, PEE, and EEE can exist in the chain. As described in Macromolecules 15, 1150 (1982), etc., the concentration of these triads and the peak intensity of the spectrum are related by the following relational expressions (1) to (6).
[PPP]=k×I(Tββ) (1)
[PPE]=k×I(Tβδ) (2)
[EPE]=k×I(Tδδ) (3)
[PEP]=k×I(Sββ) (4)
[PEE]=k×I(Sβδ) (5)
[EEE]=k×{I(Sδδ)/2+I(Sγδ)/4} (6)
where brackets [ ] indicate the fraction of triads, eg [PPP] is the fraction of PPP triads in all triads. therefore,
[PPP] + [PPE] + [EPE] + [PEP] + [PEE] + [EEE] = 1
(7)
is. Also, k is a constant and I indicates spectral intensity, for example, I(Tββ) means the intensity of the peak at 28.7 ppm attributed to Tββ. By using the relational expressions (1) to (7) above, the fraction of each triad can be obtained, and the ethylene content can be obtained by the following expression.
Ethylene content (mol%) = ([PEP] + [PEE] + [EEE]) x 100
The ethylene content is converted from mol% to wt% using the following formula.
Ethylene content (% by weight) = (28 x X/100)/{28 x X/100 + 42 x (1-X/100)} x 100
Here, X is the ethylene content in mol%.

[Other Components of Seal Layer (I)]
In the basic embodiment and the first to sixth embodiments described above, the resin composition (X) (resin compositions (X1) to (X6)) constituting the seal layer (I) includes the present Additives including hindered amine light stabilizers or UV absorbers, fillers, other resin components, and the like may be contained as long as they do not impair the effects of the invention. However, the total amount of additives, fillers, other resin components, etc. is preferably 50% by weight or less with respect to the resin composition.

When the resin composition (X) is composed of the polypropylene-based resin (A), the resin composition (X) preferably has the properties of the polypropylene-based resin (A).

As additives, antioxidants, neutralizers, light stabilizers, ultraviolet absorbers, nucleating agents, antiblocking agents, lubricants, antistatic agents, metal deactivators, etc., can be used in polypropylene resins. Various known additives can be blended.

Examples of antioxidants include phenol-based antioxidants, phosphite-based antioxidants, thio-based antioxidants, and the like. Examples of neutralizing agents include higher fatty acid salts such as calcium stearate and zinc stearate.

Nucleating agents include metal salts of aromatic carboxylic acids, metal salts of aromatic phosphates, sorbitol derivatives, nonitol derivatives, amide compounds, metal salts of rosin, and the like. Among these nucleating agents are aluminum pt-butylbenzoate, 2,2′-methylenebis(4,6-di-t-butylphenyl)sodium phosphate, 2,2′-methylenebis(4 ,6-di-t-butylphenyl)aluminum, bis(2,4,8,10-tetra-tert-butyl-6-hydroxy-12H-dibenzo[d,g][1,2,3]dioxaphospho syn-6-oxide) complex of aluminum hydroxide salt and organic compound, p-methyl-benzylidene sorbitol, p-ethyl-benzylidene sorbitol, 1,2,3-trideoxy-4,6:5,7-bis-[ (4-Propylphenyl)methylene]-nonitol, rosin sodium salt and the like can be exemplified.

Examples of lubricants include higher fatty acid amides such as stearamide. Examples of antistatic agents include fatty acid partial esters such as glycerin fatty acid monoester. Examples of metal deactivators include triazines, phosphones, epoxies, triazoles, hydrazides, oxamides and the like.

As the filler, various known fillers that can be used for polypropylene-based resins, such as inorganic fillers and organic fillers, can be blended. Examples of inorganic fillers include calcium carbonate, silica, hydrotalcite, zeolite, aluminum silicate, magnesium silicate, glass fiber and carbon fiber. Examples of organic fillers include crosslinked rubber microparticles, thermosetting resin microparticles, thermosetting resin hollow microparticles, and the like.

Examples of other resin components include elastomers such as modified polyolefins and ethylene-α-olefin copolymers, low-density polyethylenes, high-density polyethylenes, petroleum resins, and other thermoplastic resins.

The method for producing the resin composition (X) comprises polypropylene-based resin (A) (in the case of the basic embodiment and the first and second embodiments), polypropylene-based resin (A) and ethylene-α-olefin random co- Polymer (C) (in the case of the third embodiment), polypropylene resin (A) and the thermoplastic elastomer (D) (in the case of the fourth embodiment), polypropylene resin (A) and the thermoplastic resin (E) ( in the case of the fifth embodiment), or the propylene-ethylene block copolymer (F) (in the case of the sixth embodiment), and additives, fillers, other resin components, etc., are melt-kneaded; In the fifth embodiment, a melt-kneaded polypropylene resin (A), additives, fillers, other resin components, etc. are added with an ethylene-α-olefin random copolymer (C), a thermoplastic elastomer (D) or A method of dry blending the thermoplastic resin (E), adding the polypropylene resin (A) to the ethylene-α-olefin random copolymer (C), the thermoplastic elastomer (D) or the thermoplastic resin (E), adding It can be produced by dry-blending a masterbatch in which an agent, filler, other resin composition, etc. are dispersed in a carrier resin at a high concentration.

[Layer (II)]
The layer (II) contained in the decorative film of the present invention is made of a resin composition (Y) containing a polypropylene resin (B). By providing the layer (II) in the decorative film, it is possible to suppress the occurrence of poor appearance due to film breakage or roughening during three-dimensional decorative thermoforming. Thereby, the decorative film does not need to include a thermosetting resin layer having excellent thermoformability for improving the thermoformability.

<<polypropylene resin (B)>>
Next, the polypropylene-based resin (B) that constitutes the layer (II) will be described. The polypropylene-based resin (B) is preferably a resin that is more difficult to melt and relax than the polypropylene-based resin (A).

1. Melt flow rate (MFR (B)): (b1)
The melt flow rate (230° C., 2.16 kg load) (MFR(B)) of the polypropylene resin (B) must be lower than the MFR(A) of the polypropylene resin (A). That is, the following relational expression (b-1) is satisfied.
MFR(B)<MFR(A) Formula (b-1)

MFR (B)/MFR (A), which is the ratio of MFR between the polypropylene resin (B) and the polypropylene resin (A), is less than 1 (that is, MFR (B) < MFR (A)), and is preferably is 0.8 or less, more preferably 0.7 or less, still more preferably 0.5 or less, and particularly preferably 0.25 or less. When MFR(B)/MFR(A) is within the above range, good thermoformability is achieved. Although there is no lower limit for MFR(B)/MFR(A), it is preferably 0.01 or more.

MFR(B) is not particularly limited as long as it is within the above range, but is preferably 0.1 g/10 minutes or more, more preferably 0.2 g/10 minutes or more. Within the above range, the spreadability of the decorative film is good during thermoforming. Also, the MFR(B) is preferably 20 g/10 minutes or less, more preferably 15 g/10 minutes or less.

2. Melting peak temperature (Tm (B)): (b2)
The melting peak temperature Tm(B) of the polypropylene resin (B) in DSC measurement is not particularly limited, but is preferably 150° C. or higher, more preferably 155° C. or higher. When Tm(B) is within the above range, good heat resistance, scratch resistance, and solvent resistance are obtained.

Further, the melting peak temperature (Tm (B)) of the polypropylene resin (B) is preferably higher than the melting peak temperature (Tm (A)) of the polypropylene resin (A), and the following relational expression (b-2 ).
Tm(B)>Tm(A) Formula (b-2)
Within the above range, the thermoformability is improved.

3. Crystallization temperature (Tc (B)): (b3)
The crystallization temperature (Tc (B)) in DSC measurement of the polypropylene resin (B) is preferably higher than the crystallization temperature (Tc (A)) of the polypropylene resin (A), and the following relational expression (b- 3) is satisfied.
Tc(B)>Tc(A) Formula (b-3)
Within the above range, the thermoformability is improved.
Tc(B) is not particularly limited as long as it is within the above range, but is preferably 95° C. or higher, more preferably 100° C. or higher.

4. Resin composition The polypropylene-based resin (B) can be selected from metallocene catalyst-based propylene-based polymers, Ziegler-Natta catalyst-based propylene-based polymers, and the like. Ziegler-Natta catalyst-based propylene-based polymers are preferred.

The polypropylene-based resin (B) in the present invention is a propylene homopolymer (homopolypropylene), a propylene-α-olefin copolymer (random polypropylene), a propylene-α-olefin block copolymer (block polypropylene), and various other type of propylene-based polymer, or combinations thereof. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer.

In the present invention, preferred combinations with the sealing layer (I) are as follows.
In the first embodiment, the layer (II) preferably satisfies the above requirements (b1) and (b2), and in the second embodiment, the layer (II) satisfies the above requirements (b1) and (b3). Preferably, in the third to sixth embodiments, layer (II) satisfies the above requirement (b1).

[Other Components of Layer (II)]
The resin composition (Y) constituting the layer (II) contains, in addition to the polypropylene resin (B), additives containing hindered amine light stabilizers or ultraviolet absorbers, fillers, colorants, other resin components, and the like. may be included. That is, it may be a resin composition (polypropylene-based resin composition) containing a propylene-based polymer (polypropylene-based resin (B)), an additive, a filler, a colorant, other resin components, and the like. The total amount of additives, fillers, colorants, other resin components, etc. is preferably 50% by weight or less with respect to the polypropylene-based resin composition.

As the additive, an additive or the like that may be contained in the resin composition (X) constituting the sealing layer (I) can be used.

The resin composition (Y) is prepared by melt-kneading a propylene-based polymer, additives, fillers, other resin components, etc., or by melt-kneading a propylene-based polymer, additives, fillers, etc. and adding other resin components. It can be produced by a method of dry blending, a method of dry blending a masterbatch in which additives, fillers, etc. are dispersed in a carrier resin at a high concentration in addition to the propylene-based polymer and other resin components.

When the resin composition (Y) is composed of the polypropylene-based resin (B), the resin composition (Y) preferably has the properties of the polypropylene-based resin (B).

Moreover, it can be colored to impart a design property, and various coloring agents such as inorganic pigments, organic pigments, and dyes can be used for coloring. In addition, it is also possible to use luster materials such as aluminum flakes, titanium oxide flakes, and (synthetic) mica.

When the decorative molded article of the present invention is molded as a colored molded article, it is sufficient to use the coloring agent only in the decorative film, so the use of an expensive coloring agent compared to the case of coloring the entire resin molded article. can be suppressed. In addition, it is possible to suppress changes in physical properties that accompany the addition of a colorant.

[Decorative film]
The decorative film in the present invention includes a seal layer (I) containing a polypropylene resin (A) and a layer (II) containing a polypropylene resin (B). The decorative film can have various configurations other than the sealing layer (I) and layer (II). That is, the decorative film may be a two-layer film consisting of the seal layer (I) and the layer (II), or may be a multilayer film consisting of three or more layers consisting of the seal layer (I) and the layer (II) and another layer. It can be. The seal layer (I) is adhered along the resin molding (substrate). The surface of the decorative film may be textured, embossed, printed, sandblasted, scratched, or the like.

Three-dimensional decorative thermoforming has a high degree of freedom in the shape of the object to be decorated, and the edges of the decorative film are rolled up to the back side of the object to be decorated, so there are no seams, so the appearance is excellent. Various textures can be expressed by applying textures to the surface. For example, in the case of imparting texture such as embossing to a resin molding, three-dimensional decorative thermoforming may be performed using an embossed decorative film. For this reason, there are problems when molding with a molded body mold that imparts embossing, that is, a molded body mold is required for each embossing pattern, and it is very difficult and expensive to apply complicated embossing to a curved surface mold. It is possible to solve the problem of being , and to obtain a decorative molded article to which various patterns of embossing are easily applied. Further, a decorative film having a higher gloss can be obtained by mirror-finishing the decorative film by surface-transferring a mirror-like cooling roll.

In addition to the sealing layer (I) and layer (II), the multilayer film includes a surface layer, a surface decorative layer (III), a printed layer, a light shielding layer, a colored layer, a base layer, a barrier layer, and a layer provided between these layers. Can include tie layer layers and the like. The layer (II) containing the polypropylene-based resin (B) may be any layer, excluding the seal layer, among the layers constituting the multilayer film.

In the multilayer film, the layers other than the seal layer (I) and layer (II) are preferably thermoplastic resin layers, more preferably polypropylene resin layers. Layers other than the sealing layer (I) and the layer (II), as long as they can be distinguished from the sealing layer (I) and the layer (II), the MFR (230 ° C., 2.16 kg load) is not particularly limited. Each layer is preferably a layer containing no thermosetting resin. By using a thermoplastic resin, recyclability is improved, and by using a polypropylene-based resin, complication of the layer structure can be suppressed, and recyclability is further improved.

When the decorative film is a two-layer film, the sealing layer (I) constitutes the surface to be adhered to the resin molding, and the layer (II) constitutes the surface layer opposite to the surface to be adhered to the resin molding. Configure. In this case, layer (II) preferably contains a hindered amine light stabilizer and/or an ultraviolet absorber.

FIGS. 1(a) to 1(c) are explanatory diagrams schematically illustrating cross sections of embodiments of the decorative film. In FIGS. 1(a) to 1(c), the arrangement of the sealing layer (I) and the layer (II) will be specified for easy understanding, but the layer structure of the decorative film is shown in these examples. It should not be construed as limiting. In this specification, reference numeral 1 in the drawing indicates the decorative film, reference numeral 2 indicates the layer (II), reference numeral 3 indicates the sealing layer (I), and reference numeral 4 indicates the surface decoration layer (III). FIG. 1(a) shows an example in which the decorative film 1 is composed of a two-layer film, and the layer (II) 2 is laminated on the sealing layer (I) 3. FIG. The decorative film 1 in FIG. 1(b) consists of a sealing layer (I) 3, a layer (II) 2 and a surface layer, and the layer (II) and the surface layer are laminated in this order on the sealing layer (I). The decorative film 1 in FIG. 1(c) is composed of a sealing layer (I) 3, a layer (II) 2 and a surface decorative layer (III) 4, and the layer (II) and the surface decorative layer are formed on the sealing layer (I). The decoration layer (III) is laminated in this order.

8(a) to 8(c) are explanatory diagrams schematically illustrating cross sections of an embodiment of a decorative molded body 6 in which a decorative film 1 is adhered to a resin molded body 5. FIG. In FIGS. 8(a) to 8(c), the arrangement of the seal layer (I) and the layer (II) will be specified for easy understanding, but the layer structure of the decorative film 1 is exemplified. is not to be construed as being limited to FIG. 8(a) shows an example in which the decorative film 1 is made of a two-layer film, the seal layer (I) 3 is adhered to the resin molding 5, and the layer (II) is attached on the seal layer (I) 3. 2 are laminated. The decorative film 1 in FIG. 8(b) is composed of a seal layer (I) 3, a layer (II) 2 and a surface layer. ) are laminated in this order on the layer (II) and the surface layer. The decorative film 1 of FIG. 8(c) is composed of a sealing layer (I) 3, a layer (II) 2 and a surface decorative layer (III) 4, and the sealing layer (I) is adhered to the surface of the resin molding 5. Then, the layer (II) and the surface decoration layer (III) are laminated in this order on the sealing layer (I).

Another preferred embodiment of the decorative film is a multilayer film comprising a surface decorative layer (III) made of a surface decorative layer resin on the outermost surface opposite to the surface to be adhered to the resin molding. be done.

The surface decorative layer resin is preferably a thermoplastic resin, more preferably a polypropylene-based resin (H). Moreover, it is preferable that the surface decorative layer (III) contains a hindered amine light stabilizer and/or an ultraviolet absorber.

The melt flow rate (230° C., 2.16 kg load) (MFR(H)) of the polypropylene resin (H) in the present invention preferably satisfies MFR(H)>MFR(B). By setting the value within the above range, more beautiful surface gloss and texture can be expressed.

The polypropylene-based resin (H) in the present invention is a propylene homopolymer (homopolypropylene), a propylene-α-olefin copolymer (random polypropylene), a propylene-α-olefin block copolymer (block polypropylene), and various other type of propylene-based polymer, or combinations thereof. The propylene-based polymer preferably contains 50 mol % or more of polymerized units derived from a propylene monomer. The propylene-based polymer preferably does not contain polymerized units derived from a polar group-containing monomer. The polypropylene-based resin (H) is preferably homopolypropylene from the viewpoint of oil resistance, solvent resistance, scratch resistance, and the like. From the viewpoint of gloss and transparency (color development), a propylene-α-olefin copolymer is preferred. In the present invention, the polypropylene resin (H) forming the surface decorative layer (III) may be the same as or different from the polypropylene resin (A) forming the sealing layer (I).

The polypropylene resin (H) may contain additives including hindered amine light stabilizers and/or UV absorbers, fillers, other resin components, and the like. That is, it may be a resin composition (polypropylene-based resin composition) of a propylene-based polymer, an additive, a filler, other resin components, and the like. The total amount of additives, fillers, other resin components, etc. is preferably 50% by weight or less with respect to the polypropylene resin composition.

As the additive, an additive or the like that may be contained in the resin composition (X) constituting the sealing layer (I) can be used.

Polypropylene-based resin compositions are produced by melt-kneading a propylene-based polymer, additives, filler, other resin components, etc., or by melt-kneading a propylene-based polymer, additives, filler, etc., and drying other resin components. It can be produced by a method of blending, a method of dry-blending a masterbatch in which additives, fillers, etc. are dispersed in a carrier resin at a high concentration in addition to the propylene-based polymer and other resin components.

When the polypropylene-based resin (H) that constitutes the surface decorative layer (III) is a polypropylene-based resin composition, this polypropylene-based resin composition is composed of the polypropylene-based resin (A) that constitutes the sealing layer (I). It may be the same as or different from the polypropylene-based resin composition to be used.

The decorative film of the present invention preferably has a thickness of about 20 μm or more, more preferably about 50 μm or more, and even more preferably about 80 μm or more. By setting the thickness of the decorative film to such a value or more, the effect of imparting designability is improved, the stability during molding is also improved, and it becomes possible to obtain a better decorated molded product. On the other hand, the thickness of the decorative film is preferably about 2 mm or less, more preferably about 1.2 mm or less, still more preferably about 0.8 mm or less. By reducing the thickness of the decorative film to such a value or less, the time required for heating during thermoforming is shortened, thereby improving productivity and facilitating trimming of unnecessary portions.

In the decorative film of the present invention, the ratio of the thickness of the seal layer (I) to the total thickness of the decorative film is preferably 1 to 70%, and the ratio of the thickness of the layer (II) is preferably 30 to 70%. 99%. When the ratio of the thickness of the seal layer (I) to the entire decorative film is within the above range, sufficient adhesive strength can be exhibited, and scratches on the resin molded body (substrate) are prevented from appearing on the surface. can be suppressed. Further, when the ratio of the thickness of the layer (II) to the entire decorative film is within the above range, it is possible to avoid insufficient thermoformability of the decorative film.

In addition, in a multilayer film in which a surface decorative layer (III) made of a polypropylene resin (H) is provided on the outermost surface of the decorative film, the ratio of the thickness of the surface decorative layer (III) in the decorative film is , preferably 30% or less.

[Manufacturing of decorative film]
The decorative film of the present invention can be produced by various known molding methods.
For example, a method of co-extrusion molding the seal layer (I) made of the resin composition (X) and the layer (II) made of the resin composition (Y); A method of co-extrusion molding a layer, a thermal lamination method of applying heat and pressure to laminate another layer on one side of a pre-extruded layer, and a dry lamination method of laminating via an adhesive. and a wet lamination method, an extrusion lamination method and a sand lamination method in which a polypropylene-based resin is melt-extruded on one surface of one layer that has been extruded in advance. As a device for forming the decorative film, a known co-extrusion T-die molding machine or a known lamination molding machine can be used. Among these, a co-extrusion T-die molding machine is preferably used from the viewpoint of productivity.

Methods for cooling the molten decorative film extruded from the die include a method of bringing the molten decorative film into contact with one cooling roll via air discharged from an air knife unit or an air chamber unit, A method of pressing and cooling with a plurality of cooling rolls can be used.

In the case of imparting gloss to the decorative film of the present invention, a mirror-finishing method is used in which a specular cooling roll is surface-transferred onto the design surface of the decorative film of the product.

Furthermore, the surface of the decorative film of the present invention may have a textured shape. Such a decorative film is produced by a method in which a melted resin extruded from a die is directly pressed between a roll having an uneven shape and a smooth roll to transfer the uneven shape. It can be manufactured by a surface transfer method or the like in which a heated roll and a smooth cooled roll are brought into pressure contact with each other. Examples of the embossed shape include pear-skin tone, animal skin tone, hairline tone, carbon tone, and the like.

The decorative film of the present invention may be heat-treated after being formed into a film. Examples of the heat treatment method include a method of heating with a hot roll, a method of heating with a heating furnace or a far-infrared heater, and a method of blowing hot air.

[Decorative molding]
As a molded article to be decorated (to be decorated) in the present invention, it is preferable to use various resin molded articles (hereinafter sometimes referred to as "substrate") made of a polypropylene resin or a polypropylene resin composition. can. The molding method of the resin molding is not particularly limited, and examples thereof include injection molding, blow molding, press molding, and extrusion molding.

Since the polypropylene resin is non-polar, it is a difficult-to-adhere polymer. By including the layer (II) composed of the polypropylene-based resin, a very high adhesive strength is exhibited by sticking the decoration target and the decorative film made of the polypropylene resin.

As the base resin of the polypropylene-based resin and polypropylene-based resin composition of the molded article to be decorated, propylene homopolymer (homopolypropylene), propylene-α-olefin copolymer, or propylene block copolymer, etc. Various types based on various known propylene monomers can be selected. In addition, it may contain a filler such as talc for imparting rigidity and an elastomer or the like for imparting impact resistance, as long as the effects of the present invention are not impaired. In addition, it may contain additive components and other resin components in the same manner as the polypropylene-based resin composition that can constitute the decorative film described above.

The decorative molded article obtained by attaching the decorative film of the present invention to various molded articles formed in a three-dimensional shape made of polypropylene resin greatly reduces VOC contained in coatings and adhesives. , household appliances, vehicles (railroads, etc.), building materials, daily necessities, and the like.

[Manufacturing of decorative molding]
The method for manufacturing the decorated molded article of the present invention comprises the steps of preparing the above-described decorative film, preparing the resin molded article, and setting the resin molded article and the decorative film in a chamber box capable of reducing pressure. reducing the pressure in the chamber box; heating and softening the decorative film; pressing the decorative film against the resin molding; A step is included.

In three-dimensional decorative thermoforming, the object to be decorated and the decorative film are set in a decompressible chamber box, the film is heated and softened while the chamber box is decompressed, and the film is pressed against the object to be decorated. It has a basic process of attaching the decorative film to the surface of the object to be decorated by returning the inside of the chamber box to the atmospheric pressure or pressurizing it, and the film is attached under reduced pressure. As a result, it is possible to obtain a clean decorative molded article free from air pockets. In the manufacturing method of the present invention, any known technique can be used as long as the device and conditions are suitable for three-dimensional decorative thermoforming.

That is, the chamber box may contain all of the object to be decorated, the decorative film, the mechanism for pressing it, the device for heating the decorative film, etc., or the decorative film It may be a plurality of divided ones.

The mechanism for pressing the decorative film against the decorative object may be of any type, such as one that moves the decorative object, one that moves the decorative film, or one that moves both.
More specifically, representative molding methods are exemplified below.

A method of adhering a decorative film to an object to be decorated using a three-dimensional decorating thermoforming machine will be exemplified below with reference to the drawings.

As shown in FIG. 2, the three-dimensional decorating thermoforming machine of this embodiment comprises upper and lower chamber boxes 11 and 12, and the decorating film 1 is thermoformed in the two chamber boxes 11 and 12. I'm trying A vacuum circuit (not shown) and an air circuit (not shown) are connected to the upper and lower chamber boxes 11 and 12, respectively.

A jig 13 for fixing the decorative film 1 is provided between the upper and lower chamber boxes 11 and 12 . A table 14 that can be raised and lowered is installed in the lower chamber box 12, and the resin molding (to be decorated) 5 is set on this table 14 (via a jig or the like or directly). be. A heater 15 is incorporated in the upper chamber box 11 and the decorative film 1 is heated by the heater 15 . The object to be decorated 5 can use a propylene-based resin composition as a base.

As such a three-dimensional decoration thermoforming machine, a commercially available molding machine (for example, NGF series manufactured by Fuse Vacuum Co., Ltd.) can be used.

As shown in FIG. 3, first, with the upper and lower chamber boxes 11 and 12 opened, the decoration object 5 is placed on the table 14 in the lower chamber box 12, and the table 14 is lowered. Subsequently, the decorative film 1 is set on the jig 13 for fixing the film between the upper and lower chamber boxes 11 and 12 so that the seal layer (I) faces the substrate, that is, the object 5 to be decorated.

As shown in FIG. 4, after lowering the upper chamber box 11 and joining the upper and lower chamber boxes 11 and 12 to close the inside of the box, the inside of each of the chamber boxes 11 and 12 is brought into a vacuum suction state, and the heater 15 is heated. The decorative film 1 is heated by.

After the decorative film 1 is heated and softened, as shown in FIG. 5, the table 14 in the lower chamber box 12 is raised while the upper and lower chamber boxes 11 and 12 are kept in a vacuum state. The decorative film 1 is pressed against the object 5 to be decorated and covers the object 5 to be decorated. Further, as shown in FIG. 6, by opening the upper chamber box 11 to atmospheric pressure or supplying compressed air from a compressed air tank, the decorative film 1 is brought into close contact with the object 5 to be decorated with a greater force.

Subsequently, the insides of the upper and lower chamber boxes 11 and 12 are opened to atmospheric pressure, and the decorative molding 6 is taken out from the lower chamber box 12 . Finally, as illustrated in FIG. 7, unnecessary edges of the decorative film 1 around the decorative molding 6 are trimmed.

[Molding condition]
The pressure in the chamber boxes 11 and 12 may be reduced as long as air pockets are not generated, and the pressure in the chamber boxes is 10 kPa or less, preferably 3 kPa or less, and more preferably 1 kPa or less.

In addition, in the two chamber boxes 11 and 12 divided into upper and lower parts by the decorative film 1, the internal pressure of the chamber box on the side to which the decorative object 5 and the decorative film 1 are attached may be within the above range. The drawdown of the decorative film 1 can also be suppressed by changing the pressures of the chamber boxes 11 and 12.

At this time, a film made of a general polypropylene-based resin may be greatly deformed or ruptured by a slight pressure fluctuation due to a decrease in viscosity during heating.

The decorative film 1 of the present invention is not only resistant to drawdown, but also resistant to film deformation due to pressure fluctuations.

Heating of the decorative film 1 is controlled by heater temperature (output) and heating time. It is also possible to measure the surface temperature of the film with a thermometer such as a radiation thermometer and use it as a guideline for appropriate conditions.

In the present invention, in order to adhere the polypropylene-based decorative film 1 to the decoration target 5 made of polypropylene-based resin, the surface of the resin molding 5 and the decorative film 1 must be sufficiently softened or melted.

Therefore, it is necessary that the heater temperature is higher than the melting temperature of the polypropylene-based resin that constitutes the object to be decorated 5 and the polypropylene-based resin that constitutes the decorative film 1 . The heater temperature is preferably 160° C. or higher, more preferably 180° C. or higher, and most preferably 200° C. or higher.

The higher the heater temperature, the shorter the time required for heating. If the temperature of the heater becomes too high, not only the moldability deteriorates but also the resin thermally deteriorates. It is below.

An appropriate heating time varies depending on the heater temperature, but it is preferable that the polypropylene-based decorative film is heated and heated for a period of time longer than the time until the polypropylene-based decorative film starts to stretch back, which is called springback. In the basic form, the first embodiment, and the second embodiment, it is preferable that the heating is performed for a period of time up to 2 seconds after the end of stretching or longer.
In other words, the decorative film heated by the heater thermally expands when heated from a solid state, and once sagged as the crystals melt, and once the crystals melt, the molecules relax and temporarily spring back. After that, the film shows the behavior of sagging under its own weight, but after springback, the crystals of the film are completely melted and the molecules relax sufficiently, so that sufficient adhesive strength can be obtained.
Furthermore, surprisingly, the decorative film of the present invention can be strongly adhered to the substrate even if it is subjected to decorative thermoforming before the end of the unrolling, so that the thermoforming time can be shortened. , the molding can be completed before the hindered amine light stabilizer and/or the ultraviolet absorber contained in the decorative film volatilize.

On the other hand, if the heating time is too long, the film may sag under its own weight or be deformed due to the pressure difference between the upper and lower chamber boxes.

In the case of decorating a molded article having a complicated shape having irregularities or in the case of achieving higher adhesive strength, it is preferable to supply compressed air when adhering the decorative film to the substrate. The pressure in the upper chamber box when the compressed air is introduced is 150 kPa or higher, preferably 200 kPa or higher, more preferably 250 kPa or higher. Although there is no particular upper limit, the pressure is 450 kPa or less, preferably 400 kPa or less, since there is a risk of damaging the equipment if the pressure is too high.

EXAMPLES The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples.

<Test Examples 1 and 2>
(Measuring method and evaluation method of physical properties)
1. Measurement method of various physical properties (i) Melt flow rate (MFR)
Measured according to ISO 1133:1997 Conditions M at 230° C. and a load of 2.16 kg. The unit is g/10 minutes.

(ii) melting peak temperature (melting point)
Using a differential scanning calorimeter (DSC), once the temperature was raised to 200° C. and held for 10 minutes, the temperature was lowered to 40° C. at a cooling rate of 10° C./min, and again at a heating rate of 10° C./min. The temperature of the endothermic peak top at the time of measurement was taken as the melting peak temperature (melting point). The unit is °C.

(iii) Crystallization temperature Using a differential scanning calorimeter (DSC), a sheet-shaped sample piece was packed in a 5 mg aluminum pan, and the temperature was raised from 50 ° C. to 200 ° C. at a temperature increase rate of 100 ° C./min. After holding for 10 minutes, the temperature was lowered to 40°C at 10°C/min to crystallize. The crystallization maximum peak temperature at this time was defined as the crystallization temperature (Tc).

(iv) GPC measurement GPC measurement was performed using the following apparatus and conditions to calculate Mw/Mn.
・Apparatus: GPC manufactured by Waters (ALC/GPC 150C)
・ Detector: FOXBORO MIRAN 1A IR detector (measurement wavelength: 3.42 μm)
・Column: Showa Denko AD806M/S (3 columns)
・ Mobile phase solvent: ortho-dichlorobenzene (ODCB)
・Measurement temperature: 140°C
・Flow rate: 1.0 ml/min
・Injection volume: 0.2 ml
- Sample preparation: The sample was prepared as a 1 mg/mL solution using ODCB (containing 0.5 mg/mL BHT) and dissolved at 140°C for about 1 hour.

Conversion from the retention volume obtained by GPC measurement to the molecular weight was carried out using a previously prepared standard polystyrene (PS) calibration curve. The standard polystyrene used is the following brand manufactured by Tosoh Corporation.
F380, F288, F128, F80, F40, F20, F10, F4, F1, A5000, A2500, A1000
A calibration curve is generated by injecting 0.2 mL of a solution of 0.5 mg/mL each in ODCB (containing 0.5 mg/mL BHT). A cubic equation obtained by approximation by the method of least squares was used for the calibration curve.
The following numerical values were used for the viscosity formula [η]=K×M ^α used for conversion to molecular weight.
PS: K=1.38×10 ⁻⁴ , α=0.7
PP: K=1.03×10 ⁻⁴ , α=0.78

(v) Density The densities of the ethylene-α-olefin random copolymer (C) and thermoplastic elastomer (D) were measured according to the density gradient tube method of JIS K7112 (1999).

(vi) Tensile Modulus The tensile modulus of the thermoplastic elastomer (D) was measured in accordance with ASTM D638 using ASTM-IV Injection Specimen at 23° C. and a tensile speed of 50 mm/min.

(vii) ethylene content [E(C)] and [E(D)]
The ethylene content [E(C)] of the ethylene-α-olefin random copolymer (C) and the ethylene content [E(D)] of the thermoplastic elastomer (D) are determined by ¹³ C-NMR measurement based on the method described above. It was obtained from the integrated intensity obtained in . Sample preparation and measurement conditions are as follows.
200 mg of the sample ethylene-α-olefin random copolymer (C) or thermoplastic elastomer (D) was mixed with o-dichlorobenzene/deuterated brominated benzene (C ₆ D ₅ Br) = 4/1 (volume ratio ) together with 2.4 ml and hexamethyldisiloxane, which is a chemical shift reference substance, was placed in an NMR sample tube with an inner diameter of 10 mm and dissolved.
¹³ C-NMR measurement was performed using an AV400 type NMR apparatus manufactured by Bruker Biospin Co., Ltd. equipped with a cryoprobe of 10 mmφ.
The ¹³ C-NMR measurement conditions were a sample temperature of 120° C., a pulse angle of 90°, a pulse interval of 20 seconds, and an accumulation count of 512 times, and the broadband decoupling method was used.

(viii): Calculation of ethylene content of propylene-ethylene block copolymer (F), component (F1) and component (F2) The ethylene content was measured using the ¹³ C-NMR measurement method for ethylene content described above.

(ix) Isothermal crystallization time The isothermal crystallization time was measured by the method described above using a differential scanning calorimeter (DSC).
In addition, when measuring the isothermal crystallization time of the polypropylene resin (A) and the resin composition (X5), the polypropylene resin (A) and the resin composition (X5) are melt-kneaded with a twin-screw extruder. , pellets of the polypropylene resin (A) and the resin composition (X5) were obtained and used to measure the isothermal crystallization time. KZW-15 manufactured by Technovel Co., Ltd. was used for the twin-screw extruder, the screw rotation speed was 400 RPM, and the kneading temperature was set to 80 ° C., 120 ° C., and 200 ° C. from the bottom of the hopper (the same temperature until the die exit). .

2. Evaluation of physical properties of decorated molded product (1) Evaluation of thermoformability The drawdown state of the decorative film during three-dimensional decorative thermoforming and the decorative film of the decorative molded product with the decorative film attached to the substrate The adhered state was visually observed and evaluated according to the criteria shown below.
○: During the three-dimensional decorative thermoforming, the decorative film did not draw down and the base and the decorative film were in contact with each other over the entire contact surface at the same time. ing.
Δ: Since the decorative film was slightly drawn down during three-dimensional decorative thermoforming, the decorative film came into contact with the decorative film from the center of the substrate, and uneven contact occurred at the edges of the upper surface of the substrate.
x: Contact unevenness occurred over the entire surface of the substrate due to a large drawdown of the decorative film during three-dimensional decorative thermoforming.

(2) Adhesive strength between the resin molded body (substrate) and the decorative film "Craft Adhesive Tape No. 712N" manufactured by Nitoms Co., Ltd. was cut into a width of 75 mm and a length of 120 mm, and the edge of the resin molded body (substrate) was cut. The area of 75 mm×120 mm was affixed to a resin molded body (substrate) and masked (the exposed portion of the substrate surface had a width of 45 mm and a length of 120 mm). The resin molding (substrate) was placed in a three-dimensional decorative thermoforming apparatus NGF-0406-SW so that the masking surface of the resin molded body (substrate) was in contact with the decorative film, and three-dimensional decorative thermoforming was performed.

The decorative film surface of the obtained decorative molded product was cut with a cutter in a direction perpendicular to the longitudinal direction of the adhesive tape with a width of 10 mm up to the base surface to prepare a test piece. In the obtained test piece, the adhesive surface between the substrate and the decorative film had a width of 10 mm and a length of 45 mm. Attach the test piece to the tensile tester so that the base part and the decorative film part of the test piece are 180 °, measure the 180 ° peel strength of the adhesive surface at a tensile speed of 200 mm / min, and measure the maximum strength at the time of peeling or breaking (N/10 mm) was measured five times, and the average strength was taken as the adhesive strength. The test was performed at 23°C and 50% RH.

(3) Weather resistance After holding the flat plate sample after three-dimensional decorative thermoforming at 23 ° C. 50% RH for 48 hours, cut a test piece of 30 mm in length and 70 mm in width from the flat plate, Toyo Seiki Co., Ltd. Atlas tester Ci65AW 504 MJ of xenon arc lamp light was applied to the decorative film side of the decorative molding under the conditions of a black panel temperature of 89° C., a humidity of 50%, and an irradiance of 100 W/m ² . The irradiation time is as follows.
Irradiation time (1). When the decorative film contains only the hindered amine light stabilizer: 400 hr
Irradiation time (2). When the decorative film contains only UV absorber: 200hr
Irradiation time (3). When the decorative film contains both the hindered amine light stabilizer and the UV absorber: 600 hr
After irradiation, the surface of the test piece was observed and evaluated under a microscope at a magnification of 20 times. In addition, the evaluation criteria are as follows.
◯: No change is observed on the irradiated surface, or staining is slightly observed.
x: Fine cracks are observed on the irradiated surface.

(4) Evaluation of recyclability The obtained decorative molded article was pulverized, a recycled molded article was obtained by injection molding in the same manner as in the production of the resin molded article (substrate), and the appearance was visually evaluated. Those with excellent appearance were evaluated as “○”.

(Preparation of resin molding (substrate))
1. Polypropylene-Based Resins Used in Resin Molds The following polypropylene-based resins were used.
(Z-1): Propylene homopolymer (MFR = 40 g/10 min, Tm = 165°C), manufactured by Japan Polypropylene Corporation, trade name "Novatec (registered trademark) MA04H"
(Z-2): Propylene ethylene block copolymer (MFR = 30 g/10 min, Tm = 164°C), manufactured by Japan Polypropylene Corporation, trade name "Novatec (registered trademark) NBC03HR"
(Z-3): 60% by weight of polypropylene resin (Z-2), 20% by weight of EBR (Tafmer (registered trademark) A0550S manufactured by Mitsui Chemicals, Inc.) with MFR = 1.0, inorganic filler (Japan Talc P-6 manufactured by Talc Co., Ltd., average particle size 4.0 μm) is blended at 20 wt% polypropylene resin composition

2. Production of Resin Molded Article (Substrate) Using polypropylene resins (Z-1) to (Z-3), injection molded articles were obtained by the following method.
Injection molding machine: "IS100GN" manufactured by Toshiba Machine Co., Ltd., mold clamping pressure: 100 tons Cylinder temperature: 200°C
Mold temperature: 40°C
Injection mold: Width x height x thickness = 120 mm x 120 mm x 3 mm flat plate Condition adjustment: Maintained for 5 days in a constant temperature and humidity room with a temperature of 23 ° C and a humidity of 50% RH

(Test example 1)
[Materials used]
(1) Polypropylene resin The following polypropylene resin was used.
(A-1): Metallocene-catalyzed propylene-α-olefin copolymer (MFR = 7.0 g/10 min, Tm = 125°C, Mw/Mn = 2.5), manufactured by Japan Polypropylene Corporation, trade name “Wintech (registered trademark) WFX4M”
(A-2): Metallocene-catalyzed propylene-α-olefin copolymer (MFR = 25 g/10 min, Tm = 125°C, Mw/Mn = 2.4), manufactured by Japan Polypropylene Co., Ltd., trade name “Win Tech (registered trademark) WSX03”
(A-3): Metallocene-catalyzed propylene-α-olefin copolymer (MFR = 7.0 g/10 min, Tm = 135°C, Mw/Mn = 2.3), manufactured by Nippon Polypropylene Co., Ltd., trade name “Wintech (registered trademark) WFW4M”
(A-4): Metallocene-catalyzed propylene-α-olefin copolymer (MFR = 30 g/10 min, Tm = 145°C, Mw/Mn = 2.4), manufactured by Japan Polypropylene Co., Ltd., trade name “Win Tech (registered trademark) WMG03”

(B-1): Propylene homopolymer with Ziegler-Natta catalyst (MFR = 0.4 g/10 min, Tm = 161°C, Tc = 114°C, Mw/Mn = 4.9), manufactured by Japan Polypropylene Corporation , trade name “Novatec (registered trademark) EA9”
(B-2): Ziegler-Natta catalyzed propylene homopolymer (MFR = 2.4 g/10 min, Tm = 161°C, Tc = 112°C), manufactured by Japan Polypropylene Corporation, trade name Novatec (registered trademark) ) FY6”
(B-1-1): A polypropylene resin composition obtained by blending 100 parts by weight of a polypropylene resin (B-1) with 0.2 parts by weight of a hindered amine light stabilizer (manufactured by BASF Corporation, trade name "Tinuvin770"). Product (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)
(B-1-2): Polypropylene resin composition obtained by blending 100 parts by weight of polypropylene resin (B-1) with 0.2 parts by weight of a hindered amine light stabilizer (manufactured by BASF Corporation, trade name "Chimassorb 944"). Product (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)
(B-1-3): Polypropylene resin composition obtained by blending 100 parts by weight of polypropylene resin (B-1) with 0.2 parts by weight of a hindered amine light stabilizer (manufactured by ADEKA Co., Ltd., trade name "LA57"). Product (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)
(B-1-4): A polypropylene resin composition obtained by blending 0.2 parts by weight of a hindered amine light stabilizer (manufactured by ADEKA Co., Ltd., trade name "LA52") with 100 parts by weight of polypropylene resin (B-1). Product (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)
(B-1-5): A polypropylene-based resin composition obtained by blending 100 parts by weight of polypropylene-based resin (B-1) with 0.2 parts by weight of an ultraviolet absorber (manufactured by ADEKA Co., Ltd., trade name "ADEKA STAB 1413"). (MFR = 0.4 g/10 min, Tm = 161°C, Tc = 114°C)
(B-1-6): 100 parts by weight of polypropylene resin (B-1), 0.2 parts by weight of a hindered amine light stabilizer (manufactured by BASF Corporation, trade name "Tinuvin770"), and further an ultraviolet absorber ( ADEKA Co., Ltd., trade name "ADEKA STAB 1413") blended polypropylene resin composition (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)
(B-2-1): A polypropylene resin composition obtained by blending 100 parts by weight of a polypropylene resin (B-2) with 0.2 parts by weight of a hindered amine light stabilizer (manufactured by BASF Corporation, trade name "Tinuvin770"). Product (MFR = 2.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)

(H-1): Propylene homopolymer (MFR = 10 g/10 min, Tm = 161°C, Tc = 116°C, tensile modulus = 1600 MPa), manufactured by Japan Polypropylene Corporation, trade name "Novatec (registered trademark)"FA3KM"
(H-1-1): A polypropylene resin composition obtained by blending 100 parts by weight of a polypropylene resin (A-1) with 0.2 parts by weight of a hindered amine light stabilizer (manufactured by BASF Corporation, trade name "Tinuvin770"). Product (MFR = 10 g / 10 minutes, Tm = 161 ° C.)

Example 1-1
・Production of decorative film Seal layer (I) extruder-1 with a diameter of 30 mm (diameter) and layer (II) extruder-2 with a diameter of 40 mm (diameter) are connected, lip opening 0.8 mm , a two-kind, two-layer T die with a die width of 400 mm was used. The polypropylene resin (A-1) was introduced into the extruder-1 for the seal layer (I), and the polypropylene resin (B-1-1) into the extruder-2 for the layer (II), and the resin temperature was 240°C. , the extruder-1 for the seal layer (I) had a discharge rate of 4 kg/h, and the extruder-2 for the layer (II) had a discharge rate of 12 kg/h.

The melt extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the seal layer (I) with a thickness of 50 μm and a layer with a thickness of 150 μm ( A two-layer unstretched film with II) laminated was obtained.

• Three-dimensional decorative thermoforming As the resin molded body (substrate) 5, an injection molded body made of the polypropylene-based resin (Z-1) obtained above was used.
"NGF-0406-SW" manufactured by Fuse Vacuum Co., Ltd. was used as a three-dimensional decoration thermoforming apparatus. As shown in FIGS. 2 to 7, the decorative film 1 is placed so that the seal layer (I) faces the substrate (resin molded body 5) and the longitudinal direction is the MD direction of the film. and set on a film fixing jig 13 having an opening size of 210 mm×300 mm. The resin molded body 5 is placed on the table 14 located below the jig 13, and is attached onto a sample installation table with a height of 20 mm via "Nichiban Co., Ltd. NW-K15". rice field. The jig 13 and the table 14 were installed in the upper and lower chamber boxes 11 and 12, and the upper and lower chamber boxes 11 and 12 were closed to make the inside of the chamber boxes airtight. The chamber box is vertically divided through the decorative film 1. - 特許庁The upper and lower chamber boxes 11 and 12 are evacuated and the pressure is reduced from the atmospheric pressure (101.3 kPa) to 1.0 kPa. Decorative film 1 was heated. Vacuum suction was continued even during heating, and finally the pressure was reduced to 0.1 kPa. Five seconds after the completion of the springback phenomenon in which the decorative film 1 is heated and temporarily loosened and then stretched back, the table 14 installed in the lower chamber box 12 is moved upward, and the resin molded body 5 is removed. was pressed against the decorative film 1, and immediately after that, compressed air was supplied so that the pressure in the upper chamber box 11 was 270 kPa, and the resin molding 5 and the decorative film 1 were brought into close contact with each other. Thus, a three-dimensional decorated thermoformed article (decorated molded article 6) was obtained in which the decorative film 1 was adhered to the top and side surfaces of the resin molded article 5. Evaluation results are shown in Table 2-1. The evaluation of weather resistance was performed under the condition of irradiation time (1).

Example 1-2
In the production of the decorative film of Example 1-1, Example 1- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 2-1.

Example 1-3
In the production of the decorative film of Example 1-1, Example 1- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 2-1.

Examples 1-4
In the production of the decorative film of Example 1-1, Example 1- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 2-1.

Examples 1-5
In the production of the decorative film of Example 1-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-5), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 1-1, except that the condition of time (2) was used. Evaluation results are shown in Table 2-1.

Examples 1-6
In the production of the decorative film of Example 1-1, Example 1- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 2-1.

Examples 1-7
Same as Example 1-1, except that the polypropylene resin (A-1) of the sealing layer (I) was changed to the polypropylene resin (A-2) in the production of the decorative film of Example 1-1. was molded and evaluated. Evaluation results are shown in Table 2-1.

Examples 1-8
Same as Example 1-1, except that the polypropylene resin (A-1) of the sealing layer (I) was changed to the polypropylene resin (A-3) in the production of the decorative film of Example 1-1. was molded and evaluated. Evaluation results are shown in Table 2-1.

Examples 1-9
Same as Example 1-1, except that the polypropylene resin (A-1) of the sealing layer (I) was changed to the polypropylene resin (A-4) in the production of the decorative film of Example 1-1. was molded and evaluated. Evaluation results are shown in Table 2-1.

Examples 1-10
・Production of decorative film Extruder-1 for seal layer (I) with a diameter of 30 mm (diameter), extruder-2 for layer (II) with a diameter of 40 mm (diameter), and surface decoration with a diameter of 30 mm (diameter) A 3-type 3-layer T die with a lip opening of 0.8 mm and a die width of 400 mm was used, to which extruder-3 for layer (III) was connected. Polypropylene-based resin (A-1) in extruder-1 for sealing layer (I), polypropylene-based resin (B-1-1) in extruder-2 for layer (II), surface decorative layer (III) The polypropylene resin (H-1-1) was put into each extruder-3, the resin temperature was 240°C, the discharge rate of extruder-1 was 4 kg/h, the discharge rate of extruder-2 was 8 kg/h, Melt extrusion was carried out under the conditions of a discharge rate of 4 kg/h from the extruder-3.

The melt-extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the surface decoration layer (III) with a thickness of 50 μm and a surface decoration layer (III) with a thickness of 100 μm. A three-layer unstretched film was obtained in which the layer (II) and the sealing layer (I) having a thickness of 50 μm were laminated.

Using the unstretched film obtained in the production of the above-described decorated film, three-dimensional decorative thermoforming was performed in the same manner as in Example 1-1 and evaluated. Evaluation results are shown in Table 2-2.

Examples 1-11
In the production of the decorative film of Example 1-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to a polypropylene-based resin (B-1-6), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 1-1, except that the condition of time (3) was used. Evaluation results are shown in Table 2-2.

Examples 1-12
In the three-dimensional decorative thermoforming of Example 1-1, molding and evaluation were performed in the same manner as in Example 1-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-2). Evaluation results are shown in Table 2-2.

Examples 1-13
In the three-dimensional decorative thermoforming of Example 1-1, molding and evaluation were performed in the same manner as in Example 1-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-3). Evaluation results are shown in Table 2-2.

Comparative Example 1-1
Example 1-1, except that the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1) in the production of the decorative film of Example 1-1. Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 2-2.

Comparative Example 1-2
Example 1-1 except that in the production of the decorative film of Example 1-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 2-2.

Comparative Example 1-3
Same as Example 1-1, except that the polypropylene resin (A-1) of the seal layer (I) was changed to the polypropylene resin (B-1) in the production of the decorative film of Example 1-1. was molded and evaluated. Evaluation results are shown in Table 2-2.

Comparative Example 1-4
In the production of the decorative film of Example 1-1, the polypropylene-based resin (A-1) of the sealing layer (I) was changed to polypropylene-based resin (B-1), and the springback occurred in the three-dimensional decorative thermoforming. Molding and evaluation were performed in the same manner as in Example 1-1, except that molding was performed 40 seconds after the phenomenon was completed. Evaluation results are shown in Table 2-2.

Comparative Example 1-5
In the production of the decorative film of Example 1-1, the polypropylene resin (B-1-1) of layer (II) was changed to polypropylene resin (B-1-5), and the seal layer (I) Polypropylene resin (A-1) was changed to polypropylene resin (B-1), molding was performed 40 seconds after the springback phenomenon ended in three-dimensional decorative thermoforming, and irradiation was performed to evaluate weather resistance. Molding and evaluation were performed in the same manner as in Example 1-1, except that the condition of time (2) was used. Evaluation results are shown in Table 2-2.

The decorated molded articles obtained from the decorated films of Examples 1-1 to 1-13 each contained a hindered amine light stabilizer and/or an ultraviolet absorber in any layer, and the seal layer (I) The melt flow rate (MFR (A)) of the polypropylene resin (A) in the layer (II) exceeds 0.5 g / 10 minutes, and the melt flow rate (MFR (B) of the polypropylene resin (B) in the layer (II) )) is smaller than MFR(A), there is no contact unevenness, excellent thermoformability, and good adhesion. Moreover, since the decorative thermoforming was performed for a short time, volatilization of the hindered amine light stabilizer and/or the ultraviolet absorber could be reduced, and the weather resistance was excellent even after the thermoforming. Furthermore, the molded article obtained was excellent in recyclability.

On the other hand, the decorative film of Comparative Example 1-1, in which none of the layers contained a hindered amine light stabilizer and/or an ultraviolet absorber, had poor weather resistance. The decorative film of Comparative Example 1-2, in which MFR(B) was larger than MFR(A), was poor in thermoformability due to drawdown of the decorative film during three-dimensional decorative thermoforming. The obtained decorative molded article was inferior in appearance, and the adhesive strength and weather resistance were not evaluated. In Comparative Example 1-3, in which the MFR (A) was 0.5 g/10 min or less and the hindered amine light stabilizer was blended in the layer (II), molding was performed 5 seconds after the springback phenomenon ended. In this case, the heating time for the three-dimensional decorative molding was short, so good adhesiveness was not exhibited. Comparative Example 1-4, in which the same decorative film as in Comparative Example 1-3 was used and molding was performed 40 seconds after the end of the springback phenomenon, was achieved by lengthening the heating time for three-dimensional decorative molding. Adhesiveness was exhibited, but the added hindered amine light stabilizer volatilized, resulting in poor weather resistance as compared with Example 1-1. Comparative Example 1-5, in which the MFR (A) is 0.5 g/10 minutes or less and the layer (II) contains an ultraviolet absorber, increases the heating time of the three-dimensional decorative molding, and the adhesiveness is Although it developed, the added ultraviolet absorber volatilized, and the weather resistance was inferior to that of Example 1-5.

(Test example 2)
[Materials used]
In addition to the polypropylene-based resins used in (Test Example 1), the following polypropylene-based resins were used.
(A-6): Propylene-α-olefin copolymer (MFR = 5.0 g/10 min, Tc = 86°C, Mw/Mn = 4.0), manufactured by Japan Polypropylene Corporation, trade name "Novatec ( Registered trademark) FX4G”
(A-7): Propylene-α-olefin copolymer (MFR = 7.0 g/10 min, Tc = 96°C, Mw/Mn = 3.9), manufactured by Japan Polypropylene Corporation, trade name "Novatec ( Registered trademark) FW4B”
(B-1-7): A polypropylene-based resin composition obtained by blending 100 parts by weight of polypropylene-based resin (B-1) with 0.2 parts by weight of an ultraviolet absorber (manufactured by ADEKA Co., Ltd., trade name "LA-31G"). Product (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)
(B-1-8): 100 parts by weight of polypropylene resin (B-1), 0.2 parts by weight of a hindered amine light stabilizer (manufactured by BASF Corporation, trade name "Chimassorb 944"), and further an ultraviolet absorber ( ADEKA Co., Ltd., trade name "LA-31G") blended polypropylene resin composition (MFR = 0.4 g / 10 minutes, Tm = 161 ° C., Tc = 114 ° C.)

Example 2-1
In the production of the decorative film of Example 1-1, the polypropylene-based resin (A-1) of the sealing layer (I) was changed to polypropylene-based resin (A-6), and the springback occurred in the three-dimensional decorative thermoforming. Molding and evaluation were performed in the same manner as in Example 1-1, except that molding was performed 10 seconds after the phenomenon was completed. Evaluation results are shown in Table 3-1.

Example 2-2
In the production of the decorative film of Example 2-1, Example 2- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 3-1.

Example 2-3
In the production of the decorative film of Example 2-1, Example 2- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 3-1.

Example 2-4
In the production of the decorative film of Example 2-1, Example 2- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 3-1.

Examples 2-5
In the production of the decorative film of Example 2-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1-5), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 2-1, except that the condition of time (2) was used. Evaluation results are shown in Table 3-1.

Example 2-6
In the production of the decorative film of Example 2-1, Example 2- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 3-1.

Examples 2-7
Same as Example 2-1, except that the polypropylene resin (A-6) of the seal layer (I) was changed to the polypropylene resin (A-7) in the production of the decorative film of Example 2-1. was molded and evaluated. Evaluation results are shown in Table 3-1.

Example 2-8
・Production of decorative film Extruder-1 for seal layer (I) with a diameter of 30 mm (diameter), extruder-2 for layer (II) with a diameter of 40 mm (diameter), and surface decoration with a diameter of 30 mm (diameter) A 3-type 3-layer T die with a lip opening of 0.8 mm and a die width of 400 mm was used, to which extruder-3 for layer (III) was connected. Polypropylene-based resin (A-6) in extruder-1 for sealing layer (I), polypropylene-based resin (B-1-1) in extruder-2 for layer (II), surface decorative layer (III) The polypropylene resin (H-1-1) was put into each extruder-3, the resin temperature was 240°C, the discharge rate of extruder-1 was 4 kg/h, the discharge rate of extruder-2 was 8 kg/h, Melt extrusion was carried out under the conditions of a discharge rate of 4 kg/h from the extruder-3.

The melt-extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the surface decoration layer (III) with a thickness of 50 μm and a surface decoration layer (III) with a thickness of 100 μm. A three-layer unstretched film was obtained in which the layer (II) and the sealing layer (I) having a thickness of 50 μm were laminated.

Using the unstretched film obtained in the production of the above-described decorated film, three-dimensional decorative thermoforming was performed in the same manner as in Example 2-1 and evaluated. Evaluation results are shown in Table 3-1.

Example 2-9
In the production of the decorative film of Example 2-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-6), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 2-1, except that the condition of time (3) was used. Evaluation results are shown in Table 3-1.

Example 2-10
In the three-dimensional decorative thermoforming of Example 2-1, molding and evaluation were performed in the same manner as in Example 2-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-2). Evaluation results are shown in Table 3-2.

Example 2-11
In the three-dimensional decorative thermoforming of Example 2-1, molding and evaluation were performed in the same manner as in Example 2-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-3). Evaluation results are shown in Table 3-2.

Example 2-12
In the production of the decorative film of Example 2-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-7), and the weather resistance was evaluated based on the irradiation time. Molding and evaluation were performed in the same manner as in Example 2-1, except that the condition (2) was used. Evaluation results are shown in Table 3-2.

Example 2-13
In the production of the decorative film of Example 2-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1-8), and the weather resistance was evaluated based on the irradiation time. Molding and evaluation were performed in the same manner as in Example 2-1, except that the condition (3) was used. Evaluation results are shown in Table 3-2.

Comparative Example 2-1
Example 2-1 except that the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1) in the production of the decorative film of Example 2-1. Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 3-2.

Comparative example 2-2
In the production of the decorative film of Example 2-1, Example 2-1 except that the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 3-2.

Comparative example 2-3
Same as Example 2-1, except that the polypropylene resin (A-6) of the sealing layer (I) was changed to the polypropylene resin (B-1) in the production of the decorative film of Example 2-1. was molded and evaluated. Evaluation results are shown in Table 3-2.

Comparative Example 2-4
In the production of the decorative film of Example 2-1, the polypropylene-based resin (A-6) of the sealing layer (I) was changed to polypropylene-based resin (B-1), and the springback occurred in the three-dimensional decorative thermoforming. Molding and evaluation were performed in the same manner as in Example 2-1, except that molding was performed 40 seconds after the phenomenon was completed. Evaluation results are shown in Table 3-2.

Comparative Example 2-5
In the production of the decorative film of Example 2-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-5), and the seal layer (I) Polypropylene resin (A-6) was changed to polypropylene resin (B-1), molding was performed 40 seconds after the springback phenomenon ended in three-dimensional decorative thermoforming, and irradiation was performed to evaluate weather resistance. Molding and evaluation were performed in the same manner as in Example 2-1, except that the condition of time (2) was used. Evaluation results are shown in Table 3-2.

The decorated molded articles obtained from the decorated films of Examples 2-1 to 2-13 contained a hindered amine light stabilizer and/or an ultraviolet absorber in any layer, and the seal layer (I) The melt flow rate (MFR (A)) of the polypropylene resin (A) in the layer (II) exceeds 0.5 g / 10 minutes, and the melt flow rate (MFR (B) of the polypropylene resin (B) in the layer (II) )) is smaller than the MFR (A), the crystallization temperature (Tc (A)) of the polypropylene resin in the seal layer (I) is less than 100 ° C., and the polypropylene resin in the layer (II) Since the crystallization temperature (Tc(B)) of was higher than Tc(A), there was no contact unevenness, excellent thermoformability, and good adhesive strength. Moreover, since the decorative thermoforming was performed for a short time, volatilization of the hindered amine light stabilizer and/or the ultraviolet absorber could be reduced, and the weather resistance was excellent even after the thermoforming. Furthermore, the molded article obtained was excellent in recyclability.

On the other hand, the decorative film of Comparative Example 2-1, in which none of the layers contained a hindered amine light stabilizer and/or an ultraviolet absorber, had poor weather resistance. The decorative film of Comparative Example 2-2, in which MFR(B) was larger than MFR(A), had poor thermoformability due to drawdown of the decorative film during three-dimensional decorative thermoforming. The obtained decorative molded article was inferior in appearance, and the adhesive strength and weather resistance were not evaluated. In Comparative Example 2-3, in which MFR (A) was 0.5 g/10 minutes or less and the layer (II) contained a hindered amine light stabilizer, molding was performed 10 seconds after the springback phenomenon ended. In this case, the heating time for the three-dimensional decorative molding was short, so good adhesiveness was not exhibited. Comparative Example 2-4, in which the same decorative film as in Comparative Example 2-3 was used and molding was performed 40 seconds after the end of the springback phenomenon, was achieved by lengthening the heating time for three-dimensional decorative molding. Adhesiveness was exhibited, but the added hindered amine light stabilizer volatilized, resulting in inferior weather resistance compared to Example 2-1. Comparative Example 2-5, in which the MFR (A) is 0.5 g/10 minutes or less and the layer (II) contains an ultraviolet absorber, increases the heating time of the three-dimensional decorative molding, and the adhesion is However, the added ultraviolet absorber volatilized, and the weather resistance was inferior to that of Example 2-5.

(Test example 3)
[Materials used]
In addition to the resins used in (Test Example 1), the following resins were used.
(A-5): Ziegler-Natta catalyzed propylene-α-olefin copolymer (MFR = 7.0 g/10 min, Tm = 146°C, Tc = 115°C, Mw/Mn = 4.0, tensile modulus = 1200 MPa), manufactured by Japan Polypropylene Corporation, trade name “Novatec (registered trademark) FW3GT”

Ethylene-α-olefin random copolymer The following ethylene-α-olefin random copolymer was used.
(C-1): Ethylene-butene random copolymer (MFR = 6.8 g/10 min, Tm = 66°C, density = 0.885 g/cm ³ , ethylene content = 84% by weight): Mitsui Chemicals, Inc. Product name: Toughmer A4085S
(C-2): Ethylene-butene random copolymer (MFR = 7.0 g/10 min, Tm = 47°C, density = 0.860 g/cm ³ , ethylene content = 73% by weight): Mitsui Chemicals, Inc. Product name: Toughmer A4050S
(C-3): Ethylene-octene random copolymer (MFR = 2.0 g/10 min, Tm = 77°C, density = 0.885 g/cm ³ , ethylene content = 85% by weight): manufactured by DuPont Dow, Product name “Engage EG8003”
(C-4): Ethylene-octene random copolymer (MFR = 2.0 g/10 min, Tm = 38°C, density = 0.860 g/cm ³ , ethylene content = 75% by weight): manufactured by DuPont Dow, Product name “Engage EG8842”
(C-5): Ethylene-hexene random copolymer (MFR = 3.5 g/10 min, Tm = 60°C, density = 0.880 g/cm ³ , ethylene content = 76% by weight): Nippon Polyethylene Co., Ltd. Product name: Kernel KS340T
(C-6): Ethylene-propylene random copolymer (MFR = 7.0 g/10 min, Tm = 38°C, density = 0.860 g/cm ³ , ethylene content = 73% by weight): Mitsui Chemicals, Inc. Product name: Toughmer P0280

Example 3-1
In the production of the decorative film of Example 1-1, the polypropylene-based resin (A-1) of the seal layer (I) was mixed with the polypropylene-based resin (A-5) and the ethylene-α-olefin random copolymer (C- 1) and 1) are blended so that the weight ratio is 85:15, and molding is performed immediately after the springback phenomenon ends in three-dimensional decorative thermoforming (that is, the heating time after springback is 0 seconds). Molding and evaluation were carried out in the same manner as in Example 1-1 except for the above. Evaluation results are shown in Table 4-1.

Example 3-2
In the production of the decorative film of Example 3-1, Example 3- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 4-1.

Example 3-3
In the production of the decorative film of Example 3-1, Example 3- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 4-1.

Example 3-4
In the production of the decorative film of Example 3-1, Example 3- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 4-1.

Example 3-5
In the production of the decorative film of Example 3-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1-5), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 3-1, except that the condition of time (2) was used. Evaluation results are shown in Table 4-1.

Examples 3-6
In the production of the decorative film of Example 3-1, Example 3- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 4-1.

Example 3-7
In the production of the decorative film of Example 3-1, the ethylene-α-olefin random copolymer (C-1) used for the sealing layer (I) was replaced with the ethylene-α-olefin random copolymer (C-2 ), molding and evaluation were performed in the same manner as in Example 3-1. Evaluation results are shown in Table 4-1.

Example 3-8
In the production of the decorative film of Example 3-1, the ethylene-α-olefin random copolymer (C-1) used for the sealing layer (I) was replaced with the ethylene-α-olefin random copolymer (C-3 ), molding and evaluation were performed in the same manner as in Example 3-1. Evaluation results are shown in Table 4-1.

Example 3-9
In the production of the decorative film of Example 3-1, the ethylene-α-olefin random copolymer (C-1) used for the seal layer (I) was replaced with the ethylene-α-olefin random copolymer (C-4 ), molding and evaluation were performed in the same manner as in Example 3-1. Evaluation results are shown in Table 4-1.

Examples 3-10
In the production of the decorative film of Example 3-1, the ethylene-α-olefin random copolymer (C-1) used for the seal layer (I) was replaced with the ethylene-α-olefin random copolymer (C-5 ), molding and evaluation were performed in the same manner as in Example 3-1. Evaluation results are shown in Table 4-2.

Example 3-11
In the production of the decorative film of Example 3-1, the ethylene-α-olefin random copolymer (C-1) used for the seal layer (I) was replaced with the ethylene-α-olefin random copolymer (C-6 ), molding and evaluation were performed in the same manner as in Example 3-1. Evaluation results are shown in Table 4-2.

Example 3-12
In the production of the decorative film of Example 3-1, the compounding ratio of the resin of the seal layer (I) was polypropylene resin (A-5): ethylene-α-olefin random copolymer (C-1) = 70: Molding and evaluation were carried out in the same manner as in Example 3-1, except that 30 was used. Evaluation results are shown in Table 4-2.

Example 3-13
In the production of the decorative film of Example 3-1, the compounding ratio of the resin of the seal layer (I) was polypropylene resin (A-5): ethylene-α-olefin random copolymer (C-1) = 30: Molding and evaluation were performed in the same manner as in Example 3-1, except that 70 was used. Evaluation results are shown in Table 4-2.

Example 3-14
Example 3-1 except that in the production of the decorative film of Example 3-1, the polypropylene resin (A-5) used in the seal layer (I) was changed to the polypropylene resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 4-2.

Examples 3-15
・Production of decorative film Extruder-1 for seal layer (I) with a diameter of 30 mm (diameter), extruder-2 for layer (II) with a diameter of 40 mm (diameter), and surface decoration with a diameter of 30 mm (diameter) A 3-type 3-layer T die with a lip opening of 0.8 mm and a die width of 400 mm was used, to which extruder-3 for layer (III) was connected. A blend of the polypropylene resin (A-5) and the ethylene-α-olefin random copolymer (C-1) in the extruder-1 for the sealing layer (I) at a weight ratio of 85:15 was extruded. , Polypropylene-based resin (B-1-1) was introduced into extruder-2 for layer (II), and polypropylene-based resin (H-1-1) was introduced into extruder-3 for surface decorative layer (III). , the resin temperature was 240° C., the discharge rate of extruder-1 was 4 kg/h, the discharge rate of extruder-2 was 8 kg/h, and the discharge rate of extruder-3 was 4 kg/h.

The melt-extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the surface decoration layer (III) with a thickness of 50 μm and a surface decoration layer (III) with a thickness of 100 μm. A three-layer unstretched film was obtained in which the layer (II) and the sealing layer (I) having a thickness of 50 μm were laminated.

Using the unstretched film obtained in the production of the above-described decorated film, three-dimensional decorative thermoforming was performed and evaluated in the same manner as in Example 3-1. Evaluation results are shown in Table 4-2.

Example 3-16
In the production of the decorative film of Example 3-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-6), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 3-1, except that the condition of time (3) was used. Evaluation results are shown in Table 4-2.

Example 3-17
In the three-dimensional decorative thermoforming of Example 3-1, molding and evaluation were performed in the same manner as in Example 3-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-2). Evaluation results are shown in Table 4-2.

Example 3-18
In the three-dimensional decorative thermoforming of Example 3-1, molding and evaluation were performed in the same manner as in Example 3-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-3). Evaluation results are shown in Table 4-2.

Comparative Example 3-1
Example 3-1 except that in the production of the decorative film of Example 3-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (B-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 4-3.

Comparative Example 3-2
Example 3-1 except that in the production of the decorative film of Example 3-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 4-3.

Comparative Example 3-3
Molding and evaluation were carried out in the same manner as in Example 3-1, except that in the production of the decorative film of Example 3-1, the resin of the seal layer (I) was changed only to the polypropylene-based resin (B-1). rice field. Evaluation results are shown in Table 4-3.

Comparative Example 3-4
In the production of the decorative film of Example 3-1, the resin of the sealing layer (I) was changed only to the polypropylene-based resin (B-1), and after the springback phenomenon was completed in the three-dimensional decorative thermoforming, Molding and evaluation were performed in the same manner as in Example 3-1, except that molding was performed after 40 seconds. Evaluation results are shown in Table 4-3.

Comparative Example 3-5
In the production of the decorative film of Example 3-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-5), and the seal layer (I) The resin was changed to polypropylene resin (B-1) only, and molding was performed 40 seconds after the springback phenomenon ended in three-dimensional decorative thermoforming, and the weather resistance was evaluated under the irradiation time (2) conditions. Molding and evaluation were carried out in the same manner as in Example 3-1, except that . Evaluation results are shown in Table 4-3.

The decorated molded articles obtained from the decorated films of Examples 3-1 to 3-18 contained a hindered amine light stabilizer and/or an ultraviolet absorber in any layer, and the seal layer (I) The melt flow rate (MFR (A)) of the polypropylene resin (A) in the layer (II) exceeds 0.5 g / 10 minutes, and the melt flow rate (MFR (B) of the polypropylene resin (B) in the layer (II) )) is smaller than the MFR (A), and the weight ratio of the polypropylene resin (A) and the ethylene-α-olefin random copolymer (C) in the seal layer (I) is 97:3 to 5:95. In the ethylene-α-olefin random copolymer (C), (c1) an ethylene content [E(C)] of 65% by weight or more, and (c2) a density of 0.850 0.950 g/cm ³ and (c3) melt flow rate (MFR(C)) of 0.1 to 100 g/10 min. . Moreover, since the decorative thermoforming was performed for a short time, volatilization of the hindered amine light stabilizer and/or the ultraviolet absorber could be reduced, and the weather resistance was excellent even after the thermoforming. Furthermore, the obtained molded article was excellent in recyclability.

On the other hand, the decorative film of Comparative Example 3-1, in which none of the layers contained a hindered amine light stabilizer and/or an ultraviolet absorber, had poor weather resistance. The decorative film of Comparative Example 3-2, in which MFR(B) was larger than MFR(A), had poor thermoformability due to drawdown of the decorative film during three-dimensional decorative thermoforming. The obtained decorative molded article was inferior in appearance, and the adhesive strength and weather resistance were not evaluated. Comparative Example 3-3, in which the MFR (A) was 0.5 g/10 min or less and the layer (II) contained a hindered amine light stabilizer, was molded immediately after the springback phenomenon ended. Since the heating time of the original decorative molding was short, good adhesiveness was not developed. Comparative Example 3-4, in which the same decorative film as in Comparative Example 3-3 was used and molding was performed 40 seconds after the end of the springback phenomenon, was achieved by lengthening the heating time for three-dimensional decorative molding. Adhesiveness was exhibited, but the added hindered amine light stabilizer volatilized, resulting in poor weather resistance as compared with Example 3-1. Comparative Example 3-5, in which the MFR (A) is 0.5 g/10 minutes or less and the layer (II) contains an ultraviolet absorber, increases the heating time of the three-dimensional decorative molding, and the adhesion is Although it developed, the added ultraviolet absorber volatilized, and the weather resistance was inferior to that of Example 3-5.

(Test example 4)
[Materials used]
Polypropylene Resin The polypropylene resin used in (Test Example 1) and (Test Example 3) was used.

Thermoplastic elastomer (D)
The following thermoplastic elastomers were used.
(D-1): Propylene-butene random copolymer containing propylene as the main component (MFR = 7.0 g/10 min, Tm = 75°C, density = 0.885 g/cm ³ , tensile modulus = 290 MPa, propylene content = 69% by weight, butene content = 31% by weight, ethylene content [E] = 0% by weight): Mitsui Chemicals, Inc., trade name "Tafmer XM7070"
(D-2): Butene homopolymer (MFR = 5.0 g/10 min, Tm = 125°C, density = 0.915 g/cm ³ , tensile modulus = 430 MPa, ethylene content [E] = 0% by weight) : Made by Mitsui Chemicals, Inc., trade name “Tafmer BL4000”
(D-3): Propylene-ethylene-butene random copolymer containing propylene as the main component (MFR = 6.0 g/10 min, Tm = 160°C, density = 0.868 g/cm ³ , tensile modulus = 50 MPa , propylene content = 84% by weight, ethylene content [E] = 9% by weight, butene content = 7% by weight): Mitsui Chemicals, Inc., trade name "Tafmer PN2060"
(D-4): Propylene-ethylene random copolymer containing propylene as a main component (MFR = 8.0 g/10 min, Tm = 61°C, density = 0.871 g/cm ³ , tensile modulus = 45 MPa, propylene content = 89% by weight, ethylene content [E] = 11% by weight): Exxon Mobil Chemical Company, trade name "VISTAMAXX3000"

Example 4-1
In the production of the decorative film of Example 1-1, the weight ratio of the polypropylene resin (A-1) of the seal layer (I) to the polypropylene resin (A-5) and the thermoplastic elastomer (D-1) Molding and evaluation were carried out in the same manner as in Example 1-1, except that the blend was changed to 85:15. Evaluation results are shown in Table 5-1.

Example 4-2
In the production of the decorative film of Example 4-1, Example 4- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 5-1.

Example 4-3
In the production of the decorative film of Example 4-1, Example 4- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 5-1.

Example 4-4
In the production of the decorative film of Example 4-1, Example 4- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 5-1.

Example 4-5
In the production of the decorative film of Example 4-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1-5), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 4-1, except that the condition of time (2) was used. Evaluation results are shown in Table 5-1.

Example 4-6
In the production of the decorative film of Example 4-1, Example 4- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 5-1.

Examples 4-7
Example 4-1 except that the thermoplastic elastomer (D-1) used in the sealing layer (I) in the production of the decorative film of Example 4-1 was changed to the thermoplastic elastomer (D-2). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 5-1.

Examples 4-8
Example 4-1, except that the thermoplastic elastomer (D-1) used in the seal layer (I) in the production of the decorative film of Example 4-1 was changed to the thermoplastic elastomer (D-3). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 5-1.

Example 4-9
Example 4-1 except that the thermoplastic elastomer (D-1) used in the sealing layer (I) in the production of the decorative film of Example 4-1 was changed to the thermoplastic elastomer (D-4). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 5-1.

Examples 4-10
Except that in the production of the decorative film of Example 4-1, the compounding ratio of the resin of the sealing layer (I) was set to polypropylene resin (A-5):thermoplastic elastomer (D-1)=70:30. , was molded and evaluated in the same manner as in Example 4-1. Evaluation results are shown in Table 5-1.

Example 4-11
Except that in the production of the decorative film of Example 4-1, the compounding ratio of the resin of the seal layer (I) was set to polypropylene resin (A-5):thermoplastic elastomer (D-1)=30:70. , was molded and evaluated in the same manner as in Example 4-1. Evaluation results are shown in Table 5-1.

Example 4-12
Example 4-1 except that in the production of the decorative film of Example 4-1, the polypropylene resin (A-5) used in the sealing layer (I) was changed to the polypropylene resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 5-2.

Examples 4-13
・Production of decorative film Extruder-1 for seal layer (I) with a diameter of 30 mm (diameter), extruder-2 for layer (II) with a diameter of 40 mm (diameter), and surface decoration with a diameter of 30 mm (diameter) A 3-type 3-layer T die with a lip opening of 0.8 mm and a die width of 400 mm was used, to which extruder-3 for layer (III) was connected. A blend of polypropylene resin (A-5) and thermoplastic elastomer (D-1) in extruder-1 for seal layer (I) at a weight ratio of 85:15 is used for layer (II). The polypropylene resin (B-1-1) was introduced into the extruder-2, and the polypropylene resin (H-1-1) into the extruder-3 for the surface decorative layer (III). Melt extrusion was carried out under the conditions of extruder-1 discharge rate of 4 kg/h, extruder-2 discharge rate of 8 kg/h, and extruder-3 discharge rate of 4 kg/h.

The melt-extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the surface decoration layer (III) with a thickness of 50 μm and a surface decoration layer (III) with a thickness of 100 μm. A three-layer unstretched film was obtained in which the layer (II) and the sealing layer (I) having a thickness of 50 μm were laminated.

Using the unstretched film obtained in the production of the above-described decorated film, three-dimensional decorative thermoforming was performed in the same manner as in Example 4-1 and evaluated. Evaluation results are shown in Table 5-2.

Examples 4-14
In the production of the decorative film of Example 4-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-6), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 4-1, except that the condition of time (3) was used. Evaluation results are shown in Table 5-2.

Example 4-15
In the three-dimensional decorative thermoforming of Example 4-1, molding and evaluation were performed in the same manner as in Example 4-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-2). Evaluation results are shown in Table 5-2.

Example 4-16
In the three-dimensional decorative thermoforming of Example 4-1, molding and evaluation were performed in the same manner as in Example 4-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-3). Evaluation results are shown in Table 5-2.

Comparative Example 4-1
Example 4-1 except that in the production of the decorative film of Example 4-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (B-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 5-2.

Comparative Example 4-2
Example 4-1 except that in the production of the decorative film of Example 4-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 5-2.

Comparative Example 4-3
Molding and evaluation were carried out in the same manner as in Example 4-1, except that in the production of the decorative film of Example 4-1, the resin of the sealing layer (I) was changed only to the polypropylene-based resin (B-1). rice field. Evaluation results are shown in Table 5-2.

Comparative Example 4-4
In the production of the decorative film of Example 4-1, the resin of the sealing layer (I) was changed only to the polypropylene-based resin (B-1), and after the springback phenomenon was completed in the three-dimensional decorative thermoforming, Molding and evaluation were performed in the same manner as in Example 4-1, except that molding was performed after 40 seconds. Evaluation results are shown in Table 5-2.

Comparative Example 4-5
In the production of the decorative film of Example 4-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-5), and the sealing layer (I) The resin was changed to polypropylene resin (B-1) only, and molding was performed 40 seconds after the springback phenomenon ended in three-dimensional decorative thermoforming, and the weather resistance was evaluated under the irradiation time (2) conditions. Molding and evaluation were carried out in the same manner as in Example 4-1, except that . Evaluation results are shown in Table 5-2.

The decorated molded articles obtained from the decorated films of Examples 4-1 to 4-16 contained a hindered amine light stabilizer and/or an ultraviolet absorber in any layer, and the seal layer (I) The melt flow rate (MFR (A)) of the polypropylene resin (A) in the layer (II) exceeds 0.5 g / 10 minutes, and the melt flow rate (MFR (B) of the polypropylene resin (B) in the layer (II) )) is smaller than the MFR (A), and the sealing layer (I) comprises a resin composition ( X4), wherein the thermoplastic elastomer (D) is (d1) a thermoplastic elastomer containing at least one of propylene and butene as a main component, and (d2) having a density of 0.850 to 0.950 g/cm ³ , (d3) Melt flow rate (MFR (D)) is 0.1 to 100 g / 10 minutes, (d4) Tensile elastic modulus is smaller than polypropylene resin (A), so there is no contact unevenness and thermoforming The adhesive strength was excellent. Moreover, since the decorative thermoforming was performed for a short time, volatilization of the hindered amine light stabilizer and/or the ultraviolet absorber could be reduced, and the weather resistance was excellent even after the thermoforming. Furthermore, the obtained molded article was excellent in recyclability.

On the other hand, the decorative film of Comparative Example 4-1, in which none of the layers contained a hindered amine light stabilizer and/or an ultraviolet absorber, had poor weather resistance. The decorative film of Comparative Example 4-2, in which MFR(B) was larger than MFR(A), had poor thermoformability due to drawdown of the decorative film during three-dimensional decorative thermoforming. The obtained decorative molded article was inferior in appearance, and the adhesive strength and weather resistance were not evaluated. In Comparative Example 4-3, in which MFR (A) was 0.5 g/10 minutes or less and the layer (II) contained a hindered amine light stabilizer, molding was performed 5 seconds after the springback phenomenon ended. In this case, the heating time for the three-dimensional decorative molding was short, so good adhesiveness was not exhibited. Comparative Example 4-4, in which the same decorative film as in Comparative Example 4-3 was used and molding was performed 40 seconds after the end of the springback phenomenon, increased the heating time for three-dimensional decorative molding, Adhesiveness was exhibited, but the added hindered amine light stabilizer volatilized, resulting in inferior weather resistance compared to Example 4-1. Comparative Example 4-5, in which the MFR (A) is 0.5 g/10 minutes or less and the layer (II) contains an ultraviolet absorber, increases the heating time of the three-dimensional decorative molding, and the adhesiveness is Although it developed, the added ultraviolet absorber volatilized, and the weather resistance was inferior to that of Example 4-5.

(Test Example 5)
[Materials used]
Polypropylene-Based Resin As the polypropylene-based resin for the sealing layer (I), the following polypropylene-based resin was used.
(A-1): Propylene-α-olefin copolymer (MFR = 7.0 g/10 min, Tm = 125°C, crystallization initiation temperature = 97°C, isothermal crystallization time (t) = 570 seconds (107°C )), manufactured by Japan Polypropylene Co., Ltd., trade name “Wintech (registered trademark) WFX4M”
(A-5): Propylene-α-olefin copolymer (MFR = 7.0 g/10 min, Tm = 146°C, crystallization initiation temperature = 111°C, isothermal crystallization time (t) = 263 seconds (121°C )), manufactured by Japan Polypropylene Co., Ltd., trade name “Novatec (registered trademark) FW3GT”
(A-8): Propylene block copolymer (MFR = 6.0 g/10 min, Tm = 135°C, crystallization initiation temperature = 99°C, isothermal crystallization time (t) = 478 seconds (measured at 109°C) ), manufactured by Japan Polypropylene Co., Ltd., trade name “Wellnex (registered trademark) RFG4VA”
(H-1): Propylene homopolymer (MFR = 10 g/10 min, Tm = 161°C, crystallization initiation temperature = 123°C, isothermal crystallization time (t) = 613 seconds (measured at 133°C)), Japan Polypro Co., Ltd., trade name “Novatec (registered trademark) FA3KM”

The polypropylene-based resin used in (Test Example 1) was used for the layer (II) and the surface decorative layer (III).

Thermoplastic resin (E)
The following thermoplastic resins were used.
(E-1): Hydrogenated styrene elastomer (HSBR): manufactured by JSR Corporation, trade name "Dynalon 1320P"
(E-2): Styrene-based elastomer (SEBS): manufactured by Kraton Polymer Japan Co., Ltd., trade name "Kraton G1645"
(E-3): Alicyclic hydrocarbon resin: manufactured by Arakawa Chemical Co., Ltd., trade name "Arcon-P125"

Example 5-1
In the production of the decorative film of Example 1-1, the weight ratio of the polypropylene resin (A-1) of the seal layer (I) to the polypropylene resin (A-5) and the thermoplastic resin (E-1) was changed to a blend so that the ratio was 50:50, and molding was performed immediately after the springback phenomenon was completed in three-dimensional decorative thermoforming (that is, the heating time after springback was 0 seconds). Molding and evaluation were performed in the same manner as in Example 1-1. Evaluation results are shown in Table 6-1.

Example 5-2
In the production of the decorative film of Example 5-1, Example 5- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 6-1.

Example 5-3
In the production of the decorative film of Example 5-1, Example 5- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 6-1.

Example 5-4
In the production of the decorative film of Example 5-1, Example 5- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 6-1.

Example 5-5
In the production of the decorative film of Example 5-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-5), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 5-1, except that the condition of time (2) was used. Evaluation results are shown in Table 6-1.

Example 5-6
In the production of the decorative film of Example 5-1, Example 5- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 6-1.

Examples 5-7
Example 5-1 except that the thermoplastic resin (E-1) used for the seal layer (I) in the production of the decorative film of Example 5-1 was changed to the thermoplastic resin (E-2) Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 6-1.

Examples 5-8
In the production of the decorative film of Example 5-1, the thermoplastic resin (E-1) used for the seal layer (I) was changed to a thermoplastic resin (E-3), and a polypropylene resin (A-5 ) and the thermoplastic resin (E-3) were set to 85:15, molding and evaluation were carried out in the same manner as in Example 5-1. Evaluation results are shown in Table 6-1.

Examples 5-9
Except that in the production of the decorative film of Example 5-1, the compounding ratio of the resin of the sealing layer (I) was set to polypropylene resin (A-5):thermoplastic resin (E-1)=70:30. , molding and evaluation were performed in the same manner as in Example 5-1. Evaluation results are shown in Table 6-1.

Examples 5-10
Except that in the production of the decorative film of Example 5-1, the compounding ratio of the resin of the seal layer (I) was set to polypropylene resin (A-5): thermoplastic resin (E-1) = 30:70. , molding and evaluation were performed in the same manner as in Example 5-1. Evaluation results are shown in Table 6-1.

Examples 5-11
Example 5-1 except that in the production of the decorative film of Example 5-1, the polypropylene resin (A-5) used for the sealing layer (I) was changed to the polypropylene resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 6-2.

Examples 5-12
Example 5-1 except that in the production of the decorative film of Example 5-1, the polypropylene resin (A-5) used for the seal layer (I) was changed to the polypropylene resin (A-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 6-2.

Examples 5-13
In the production of the decorative film of Example 5-1, the polypropylene resin (A-5) used for the seal layer (I) was changed to polypropylene resin (A-8), and polypropylene resin (A-8 ) and the thermoplastic resin (E-1) was set to 70:30, molding and evaluation were performed in the same manner as in Example 5-1. Evaluation results are shown in Table 6-2.

Examples 5-14
・Production of decorative film Extruder-1 for seal layer (I) with a diameter of 30 mm (diameter), extruder-2 for layer (II) with a diameter of 40 mm (diameter), and surface decoration with a diameter of 30 mm (diameter) A 3-type 3-layer T die with a lip opening of 0.8 mm and a die width of 400 mm was used, to which extruder-3 for layer (III) was connected. A blend of the polypropylene resin (A-5) and the thermoplastic resin (E-1) in the extruder-1 for the sealing layer (I) so that the weight ratio is 50: 50 is used for the layer (II) The polypropylene resin (B-1-1) was introduced into the extruder-2, and the polypropylene resin (H-1-1) into the extruder-3 for the surface decorative layer (III). Melt extrusion was carried out under the conditions of extruder-1 discharge rate of 4 kg/h, extruder-2 discharge rate of 8 kg/h, and extruder-3 discharge rate of 4 kg/h.

The melt-extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the surface decoration layer (III) with a thickness of 50 μm and a surface decoration layer (III) with a thickness of 100 μm. A three-layer unstretched film was obtained in which the layer (II) and the sealing layer (I) having a thickness of 50 μm were laminated.

Using the unstretched film obtained in the production of the above-described decorated film, three-dimensional decorative thermoforming was performed and evaluated in the same manner as in Example 5-1. Evaluation results are shown in Table 6-2.

Examples 5-15
In the production of the decorative film of Example 5-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-6), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 5-1, except that the condition of time (3) was used. Evaluation results are shown in Table 6-2.

Examples 5-16
In the three-dimensional decorative thermoforming of Example 5-1, molding and evaluation were performed in the same manner as in Example 5-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-2). Evaluation results are shown in Table 6-2.

Examples 5-17
In the three-dimensional decorative thermoforming of Example 5-1, molding and evaluation were performed in the same manner as in Example 5-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-3). Evaluation results are shown in Table 6-2.

Comparative Example 5-1
In the production of the decorative film of Example 5-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1), as in Example 5-1. Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 6-2.

Comparative Example 5-2
Example 5-1 except that in the production of the decorative film of Example 5-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 6-2.

The decorated molded articles obtained from the decorated films of Examples 5-1 to 5-17 contained a hindered amine light stabilizer and/or an ultraviolet absorber in any layer, and the seal layer (I) The melt flow rate (MFR (A)) of the polypropylene resin (A) in the layer (II) exceeds 0.5 g / 10 minutes, and the melt flow rate (MFR (B) of the polypropylene resin (B) in the layer (II) )) is smaller than the MFR (A), and the seal layer (I) comprises a resin composition ( X5), wherein the thermoplastic resin (E) contains (e1) at least one of an alicyclic hydrocarbon group and an aromatic hydrocarbon group, and (x1) an isothermal crystal of the resin composition (X5) Since the crystallization time (t (X5)) (seconds) is 1.5 times or more the isothermal crystallization time (t (A)) (seconds) of the polypropylene resin (A), there is no contact unevenness and thermoformability was excellent, and the adhesive strength was good. Moreover, since the decorative thermoforming was performed for a short time, volatilization of the hindered amine light stabilizer and/or the ultraviolet absorber could be reduced, and the weather resistance was excellent even after the thermoforming. Furthermore, the molded article obtained was excellent in recyclability.

On the other hand, the decorative film of Comparative Example 5-1, in which none of the layers contained a hindered amine light stabilizer and/or an ultraviolet absorber, had poor weather resistance. The decorative film of Comparative Example 5-2, in which MFR(B) was larger than MFR(A), had poor thermoformability due to drawdown of the decorative film during three-dimensional decorative thermoforming. The obtained decorative molded article was inferior in appearance, and the adhesive strength and weather resistance were not evaluated.

(Test example 6)
[Materials used]
In addition to the polypropylene-based resins used in (Test Example 1), the following polypropylene-based resins were used.

Production of Propylene-Ethylene Block Copolymer (F) As the propylene-ethylene block copolymer (F) used for the sealing layer (I) of the decorative film, the propylene-ethylene block copolymer obtained in the following production example (F-1) to (F-4) were used. Polymerization conditions and polymerization results are shown in Table 7-1, and polymer analysis results are shown in Table 7-2.

[Production Example F-1: Production of propylene-ethylene block copolymer (F-1)]
Analysis of catalyst composition Ti content: A sample was weighed accurately, hydrolyzed and measured using a colorimetric method. For the prepolymerized sample, the content was calculated using the weight excluding the prepolymerized polymer.
Silicon compound content: Samples were accurately weighed and digested with methanol. The silicon compound concentration in the resulting methanol solution was determined by comparison with a standard sample using gas chromatography. The silicon compound content in the sample was calculated from the silicon compound concentration in methanol and the weight of the sample. For the prepolymerized sample, the content was calculated using the weight excluding the prepolymerized polymer.

Preparation of Prepolymerized Catalyst (1) Preparation of Solid Catalyst A 10 L capacity autoclave equipped with a stirring device was sufficiently purged with nitrogen, and 2 L of purified toluene was introduced. At room temperature, 200 g of magnesium diethoxide [Mg(OEt) ₂ ] was added, and 1 L of titanium tetrachloride (TiCl ₄ ) was slowly added. The temperature was raised to 90° C. and 50 ml of di-n-butyl phthalate were introduced. After that, the temperature was raised to 110° C. and the reaction was carried out for 3 hours. The reaction product was thoroughly washed with purified toluene. Next, refined toluene was introduced to adjust the total liquid volume to 2 L. 1 L of TiCl ₄ was added at room temperature, the temperature was raised to 110° C. and the reaction was carried out for 2 hours. The reaction product was thoroughly washed with purified toluene. Next, refined toluene was introduced to adjust the total liquid volume to 2 L. 1 L of TiCl ₄ was added at room temperature, the temperature was raised to 110° C. and the reaction was carried out for 2 hours. The reaction product was thoroughly washed with purified toluene. Further, purified n-heptane was used to replace toluene with n-heptane to obtain a slurry of solid components. A portion of this slurry was sampled and dried. An analysis revealed that the Ti content of the solid component was 2.7% by weight.

Next, an autoclave with a capacity of 20 L equipped with a stirring device was sufficiently purged with nitrogen, and 100 g of the solid component slurry was introduced as a solid component. Purified n-heptane was introduced to adjust the solid component concentration to 25 g/L. 50 ml of silicon tetrachloride (SiCl ₄ ) was added and reacted at 90° C. for 1 hour. The reaction product was thoroughly washed with purified n-heptane.

Thereafter, purified n-heptane was introduced to adjust the liquid level to 4L. 30 ml of dimethyldivinylsilane, 30 ml of diisopropyldimethoxysilane [i-Pr ₂ Si(OMe) ₂ ], and 80 g of Et ₃ Al diluted with triethylaluminum (Et ₃ Al) in n-heptane were added thereto. for 2 hours. The reaction product was thoroughly washed with purified n-heptane to obtain a solid catalyst. A part of the resulting solid catalyst slurry was sampled, dried and analyzed. The solid catalyst contained 1.2% by weight of Ti and 8.9% by weight of i-Pr ₂ Si(OMe) ₂ .

(2) Prepolymerization Using the solid catalyst obtained above, prepolymerization was performed according to the following procedure. Refined n-heptane was introduced into the above slurry to adjust the solid catalyst concentration to 20 g/L. After cooling the slurry to 10° C., 10 g of Et ₃ Al diluted in n-heptane was added as Et ₃ Al and 280 g of propylene was fed over 4 hours. After the propylene supply was finished, the reaction was continued for an additional 30 minutes. Then, the gas phase was sufficiently purged with nitrogen, and the reaction product was thoroughly washed with purified n-heptane. The resulting slurry was extracted from the autoclave and dried in a vacuum to obtain a prepolymerized catalyst. This prepolymerized catalyst contained 2.5 grams of polypropylene per gram of solid catalyst. Analysis revealed that the portion of the prepolymerized catalyst excluding polypropylene contained 1.0% by weight of Ti and 8.3% by weight of i-Pr ₂ Si(OMe) ₂ .
Using this prepolymerization catalyst, a propylene-ethylene block copolymer (F) was produced according to the following procedure.

(3) Production of propylene-ethylene block copolymer (F) Propylene-ethylene block copolymer (F) was produced using a two-tank continuous polymerization facility in which two fluidized bed polymerization tanks having an internal volume of 2 m ³ were connected in series. was manufactured. The conditions for producing the propylene-ethylene block copolymer (F-1) are as described in 6A-1 of Table 7-1. The propylene, ethylene, hydrogen and nitrogen used were purified using a common purification catalyst. The production amount of the component (F1) in the first polymerization tank and the production amount of the component (F2) in the second polymerization tank were obtained from the cooling water temperature of the heat exchanger used for temperature control of the polymerization tank.

First Polymerization Step: Production of Component (F1) Consisting of Propylene Homopolymer Propylene was homopolymerized using the first polymerization tank. The polymerization temperature was 65° C., the total pressure was 3.0 MPaG (gauge pressure, hereinafter the same), and the powder hold amount was 40 kg. Propylene, hydrogen and nitrogen were continuously supplied to the polymerization tank, and the concentrations of propylene and hydrogen were adjusted to 70.83 mol % and 0.92 mol %, respectively. As a co-catalyst, Et ₃ Al was continuously fed at a rate of 5.0 g/hour. The prepolymerized catalyst obtained above was continuously supplied to the polymerization tank so that the production amount of the component (F1) in the first polymerization tank was 20.0 kg/hour. The produced component (F1) was continuously extracted and adjusted so that the powder hold amount was constant at 40 kg. The component (F1) withdrawn from the first polymerization tank was continuously supplied to the second polymerization tank, and the production of the component (F2) consisting of the propylene-ethylene random copolymer was continued.

Second Polymerization Step: Production of Propylene-Ethylene Random Copolymer Component (F2) Random copolymerization of propylene and ethylene was carried out using the second polymerization tank. The polymerization temperature was 65° C., the total pressure was 2.0 MPaG, and the powder hold amount was 40 kg. Propylene, ethylene, hydrogen, and nitrogen were continuously supplied to the polymerization tank, and the concentrations of propylene, ethylene, and hydrogen were adjusted to 54.29 mol%, 17.14 mol%, and 0.41 mol%, respectively. . By continuously supplying ethanol as a polymerization inhibitor, the production amount of the propylene-ethylene random copolymer component (F2) in the second polymerization tank was adjusted to 6.7 kg/h. The propylene-ethylene block copolymer (F) thus produced was continuously extracted and adjusted so that the powder hold amount was constant at 40 kg. The propylene-ethylene block copolymer (F) extracted from the second polymerization tank was further transferred to a dryer and thoroughly dried.

A portion of the produced propylene-ethylene block copolymer (F) was analyzed and found to have an MFR (F) of 7.0 g/10 min and an ethylene content E (F) of 9.5% by weight. The weight ratio W(F1) of the component (F1) and the weight ratio W(F2) of the component (F2) were obtained from the production amount in the first polymerization step and the production amount in the second polymerization step, and each was 75% by weight. , 25% by weight.

The ethylene content E (F2) of the propylene-ethylene random copolymer component (F2) was calculated from W (F1), W (F2), and E (F) thus obtained.
The following formula was used for the calculation.
E(F2)={E(F)-E(F1)×W(F1)/100}÷
(W(F2)/100)
(Here, since the component (F1) is a propylene homopolymer, E (F1) is 0% by weight. In the above formula, the above formula for E (F) is rearranged for E (F2). It is what was done.)
The ethylene content E (F2) was 38.0% by weight.

[Production Examples F-2 and F-3: Production of propylene-ethylene block copolymers (F-2) and (F-3)]
A propylene-ethylene block copolymer ( F-2) and (F-3) were produced.

[Production Example F-4: Production of propylene-ethylene block copolymer F-4)]
Preparation of prepolymerized catalyst (1) Chemical treatment of silicate 3.75 liters of distilled water and then 2.5 kg of concentrated sulfuric acid (96%) were slowly added to a 10 liter separable glass flask equipped with a stirring blade. did. At 50° C., 1 kg of montmorillonite (Benclay SL manufactured by Mizusawa Chemical; average particle size=25 μm, particle size distribution=10 to 60 μm) was dispersed, heated to 90° C., and maintained at that temperature for 6.5 hours. After cooling to 50°C, the slurry was filtered under reduced pressure to collect a cake. The cake was reslurried by adding 7 liters of distilled water and filtered. This washing operation was carried out until the pH of the washing liquid (filtrate) exceeded 3.5. The collected cake was dried overnight at 110° C. under a nitrogen atmosphere. The weight after drying was 707 g.

(2) Drying of silicate The previously chemically treated silicate was dried using a kiln dryer. Specifications and drying conditions are as follows.
Rotating cylinder: Cylindrical, inner diameter 50 mm, heating zone 550 mm (electric furnace)
Rotation speed with scraping blade: 2 rpm
Tilt angle: 20/520
Feed rate of silicate: 2.5 g/min Gas flow rate: Nitrogen 96 l/h Countercurrent drying temperature: 200°C (powder temperature)

(3) Preparation of catalyst An autoclave having an internal volume of 16 liters equipped with a stirring and temperature control device was sufficiently purged with nitrogen. Here, 200 g of dry silicate was introduced, 1,160 ml of mixed heptane, and 840 ml of triethylaluminum heptane solution (0.60 M) were further added and stirred at room temperature. After 1 hour, the mixture was washed with mixed heptane to prepare a silicate slurry of 2,000 ml. Next, 9.6 ml of a heptane solution (0.71 M) of triisobutylaluminum was added to the previously prepared silicate slurry and reacted at 25° C. for 1 hour. In parallel, 2,180 mg (0.3 mM) of (r)-dichloro[1,1′-dimethylsilylenebis{2-methyl-4-(4-chlorophenyl)-4H-azulenyl}]zirconium and 870 ml of heptane were added. , 33.1 ml of a heptane solution (0.71 M) of triisobutylaluminum was added, and the mixture was allowed to react at room temperature for 1 hour. The mixture was added to the silicate slurry and stirred for 1 hour. was prepared to

(4) Prepolymerization/Washing Subsequently, the temperature inside the tank was raised by 40° C., and when the temperature was stabilized, propylene was supplied at a rate of 100 g/hour to maintain the temperature. After 4 hours the propylene feed was stopped and maintained for an additional 2 hours.
After the prepolymerization was completed, the residual monomer was purged, the stirring was stopped, and the mixture was allowed to stand for about 10 minutes, after which 2,400 ml of the supernatant was decanted. Subsequently, 9.5 ml of a heptane solution of triisobutylaluminum (0.71 M) and 5600 ml of mixed heptane were added, stirred at 40° C. for 30 minutes, allowed to stand for 10 minutes, and then 5600 ml of the supernatant was removed. Furthermore, this operation was repeated 3 times. When the final supernatant was analyzed for components, the concentration of the organoaluminum component was 1.23 mmol/liter, and the concentration of zirconium (Zr) was 8.6 × 10 ^-6 g/L. The abundance of was 0.016%. Subsequently, after adding 170 ml of a heptane solution of triisobutylaluminum (0.71 M), drying was performed under reduced pressure at 45°C. A prepolymerized catalyst containing 2.0 g of polypropylene per g of catalyst was obtained.

(5) Production of propylene-ethylene block copolymer (F) First polymerization step: Production of component (F1) consisting of propylene-ethylene random copolymer Horizontal reactor having stirring blades (L/D = 6, contents 100 liters) was sufficiently dried, and the inside was sufficiently replaced with nitrogen gas. In the presence of a polypropylene powder bed, while stirring at a rotation speed of 30 rpm, the prepolymerized catalyst prepared in the upstream part of the reactor (as a solid catalyst amount excluding the prepolymerized powder) was 0.444 g / hour, and triisobutylaluminum was added. It was fed continuously at 15.0 mmol/hour. The temperature of the reactor is maintained at 65°C and the pressure at 2.00 MPaG, and the monomer mixed gas is continuously reacted so that the gas phase in the reactor has an ethylene/propylene molar ratio of 0.058 and a hydrogen concentration of 150 ppm. Gas phase polymerization was carried out by circulating in the vessel. The polymer powder produced by the reaction was continuously withdrawn from the downstream portion of the reactor so that the amount of powder bed in the reactor was constant. At this time, the amount of polymer withdrawn when the steady state was reached was 10.0 kg/hour.
Analysis of the propylene-ethylene random copolymer obtained in the first polymerization step revealed that the ethylene content was 1.7% by weight.

Second polymerization step: Production of component (F2) composed of propylene-ethylene random copolymer Propylene extracted from the first polymerization step was placed in a horizontal reactor (L/D = 6, internal volume: 100 liters) having a stirring blade. Ethylene copolymer was fed continuously. While stirring at a rotation speed of 25 rpm, the temperature of the reactor was kept at 70 ° C., the pressure was kept at 1.88 MPaG, and the ethylene / propylene molar ratio in the gas phase part in the reactor was 0.450, and the hydrogen concentration was 300 ppm. A gas phase polymerization was carried out by continuously circulating the monomer mixed gas in the reactor. The polymer powder produced by the reaction was continuously withdrawn from the downstream portion of the reactor so that the amount of powder bed in the reactor was constant. At this time, oxygen was supplied as an activity inhibitor so that the amount of polymer withdrawn was 18.0 kg/hour, and the amount of polymerization reaction in the second polymerization step was controlled.
The propylene-ethylene block copolymer (F-4) thus obtained was analyzed and found to have an MFR of 7.0 g/10 min and an ethylene content of 6.3% by weight.

The results of polymer analysis of the propylene-ethylene block copolymers (F-1) to (F-4) are shown in Table 7-2.

Pelletization of propylene-ethylene block copolymer (F) Tetrakis[methylene-3- (3′,5′-di-t-butyl-4-hydroxyphenyl)propionate]methane 0.05 parts by weight, tris(2,4-di-t-butylphenyl)phosphite 0.10 parts by weight, calcium stearate 0.05 part by weight of each was mixed and homogenized in a tumbler, and the resulting mixture was melt-kneaded at 230°C by a twin-screw extruder with a diameter of 35 mm to obtain propylene-ethylene block copolymers F-1 to F-4. Each pellet was obtained.

Example 6-1
In the production of the decorative film of Example 1-1, the polypropylene-based resin (A-1) of the seal layer (I) was changed to a propylene-ethylene block copolymer (F-1), and three-dimensional decorative heat was applied. Molding and evaluation were performed in the same manner as in Example 1-1, except that the molding was performed immediately after the springback phenomenon ended in molding (that is, the heating time after springback was 0 seconds). Evaluation results are shown in Table 8-1.

Example 6-2
In the production of the decorative film of Example 6-1, Example 6- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 8-1.

Example 6-3
In the production of the decorative film of Example 6-1, Example 6- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 8-1.

Example 6-4
In the production of the decorative film of Example 6-1, Example 6- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 8-1.

Example 6-5
In the production of the decorative film of Example 6-1, the polypropylene resin (B-1-1) of the layer (II) was changed to the polypropylene resin (B-1-5), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 6-1, except that the condition of time (2) was used. Evaluation results are shown in Table 8-1.

Example 6-6
In the production of the decorative film of Example 6-1, Example 6- Molding and evaluation were performed in the same manner as in 1. Evaluation results are shown in Table 8-1.

Examples 6-7
In the production of the decorative film of Example 6-1, the propylene-ethylene block copolymer (F-1) used for the sealing layer (I) was changed to propylene-ethylene block copolymer (F-2). Except for this, molding and evaluation were performed in the same manner as in Example 6-1. Evaluation results are shown in Table 8-1.

Examples 6-8
In the production of the decorative film of Example 6-1, the propylene-ethylene block copolymer (F-1) used for the sealing layer (I) was changed to propylene-ethylene block copolymer (F-3). Except for this, molding and evaluation were performed in the same manner as in Example 6-1. Evaluation results are shown in Table 8-1.

Examples 6-9
In the production of the decorative film of Example 6-1, the propylene-ethylene block copolymer (F-1) used for the sealing layer (I) was changed to propylene-ethylene block copolymer (F-4). Except for this, molding and evaluation were performed in the same manner as in Example 6-1. Evaluation results are shown in Table 8-1.

Examples 6-10
・Production of decorative film Extruder-1 for seal layer (I) with a diameter of 30 mm (diameter), extruder-2 for layer (II) with a diameter of 40 mm (diameter), and surface decoration with a diameter of 30 mm (diameter) A 3-type 3-layer T die with a lip opening of 0.8 mm and a die width of 400 mm was used, to which extruder-3 for layer (III) was connected. Propylene-ethylene block copolymer (F-1) in extruder-1 for seal layer (I), polypropylene resin (B-1-1) in extruder-2 for layer (II), surface decoration The polypropylene resin (H-1-1) was put into each extruder-3 for layer (III), the resin temperature was 240 ° C., the discharge rate of extruder-1 was 4 kg / h, and the discharge rate of extruder-2 was Melt extrusion was carried out under the conditions of 8 kg/h and a discharge rate of extruder-3 of 4 kg/h.

The melt-extruded film is cooled and solidified on a cooling roll rotating at 80 ° C. and 3 m / min so that the seal layer (I) is in contact with the surface decoration layer (III) with a thickness of 50 μm and a surface decoration layer (III) with a thickness of 100 μm. A three-layer unstretched film was obtained in which the layer (II) and the sealing layer (I) having a thickness of 50 μm were laminated.

Using the unstretched film obtained in the production of the above-described decorated film, three-dimensional decorative thermoforming was performed in the same manner as in Example 6-1 and evaluated. Evaluation results are shown in Table 8-2.

Examples 6-11
In the production of the decorative film of Example 6-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-6), and the weather resistance was evaluated by irradiation. Molding and evaluation were performed in the same manner as in Example 6-1, except that the condition of time (3) was used. Evaluation results are shown in Table 8-2.

Examples 6-12
In the three-dimensional decorative thermoforming of Example 6-1, molding and evaluation were performed in the same manner as in Example 6-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-2). Evaluation results are shown in Table 8-2.

Examples 6-13
In the three-dimensional decorative thermoforming of Example 6-1, molding and evaluation were performed in the same manner as in Example 6-1, except that the substrate was changed to an injection molded body made of polypropylene resin (Z-3). Evaluation results are shown in Table 8-2.

Comparative Example 6-1
Example 6-1 except that in the production of the decorative film of Example 6-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (B-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 8-2.

Comparative Example 6-2
Example 6-1 except that in the production of the decorative film of Example 6-1, the polypropylene-based resin (B-1-1) of the layer (II) was changed to the polypropylene-based resin (H-1). Molding and evaluation were performed in the same manner. Evaluation results are shown in Table 8-2.

Comparative Example 6-3
Example 6 except that in the production of the decorative film of Example 6-1, the propylene-ethylene block copolymer (F-1) of the sealing layer (I) was changed to the polypropylene resin (B-1). Molding and evaluation were performed in the same manner as in -1. Evaluation results are shown in Table 8-2.

Comparative Example 6-4
In the production of the decorative film of Example 6-1, the propylene-ethylene block copolymer (F-1) of the seal layer (I) was changed to a polypropylene resin (B-1), and three-dimensional decorative heat was applied. Molding and evaluation were carried out in the same manner as in Example 6-1, except that molding was performed 40 seconds after the springback phenomenon ended in molding. Evaluation results are shown in Table 8-2.

Comparative Example 6-5
In the production of the decorative film of Example 6-1, the polypropylene-based resin (B-1-1) of layer (II) was changed to polypropylene-based resin (B-1-5), and the seal layer (I) The propylene-ethylene block copolymer (F-1) was changed to a polypropylene resin (B-1), and molding was performed 40 seconds after the springback phenomenon ended in three-dimensional decorative thermoforming. Molding and evaluation were performed in the same manner as in Example 6-1, except that the evaluation was performed under the conditions of the irradiation time (2). Evaluation results are shown in Table 8-2.

The decorated molded articles obtained from the decorated films of Examples 6-1 to 6-13 each contained a hindered amine light stabilizer and/or an ultraviolet absorber in any layer, and the seal layer (I) The melt flow rate (MFR (A)) of the polypropylene resin (A) in the layer (II) exceeds 0.5 g / 10 minutes, and the melt flow rate (MFR (B) of the polypropylene resin (B) in the layer (II) )) is smaller than the MFR (A), the polypropylene resin (A) is a propylene-ethylene block copolymer (F), and the copolymer (F) has (f1) a melting peak temperature (Tm ( F)) is 110 to 170° C., (f2) 5 to 97% by weight of component (F1) consisting of propylene homopolymer or propylene-ethylene random copolymer, and propylene having a higher ethylene content than component (F1) - Since the component (F2) comprising an ethylene random copolymer was contained in an amount of 3 to 95% by weight, there was no contact unevenness, the thermoformability was excellent, and the adhesive strength was good. Moreover, since the decorative thermoforming was performed for a short time, volatilization of the hindered amine light stabilizer and/or the ultraviolet absorber could be reduced, and the weather resistance was excellent even after the thermoforming. Furthermore, the molded article obtained was excellent in recyclability.

On the other hand, the decorative film of Comparative Example 6-1, in which none of the layers contained a hindered amine light stabilizer and/or an ultraviolet absorber, had poor weather resistance. The decorative film of Comparative Example 6-2, in which MFR(B) was larger than MFR(A), had poor thermoformability due to drawdown of the decorative film during three-dimensional decorative thermoforming. The obtained decorative molded article was inferior in appearance, and the adhesive strength and weather resistance were not evaluated. Comparative Example 6-3, in which the MFR (A) was 0.5 g/10 min or less and the layer (II) contained a hindered amine light stabilizer, was molded immediately after the springback phenomenon ended. Since the heating time of the original decorative molding was short, good adhesiveness was not developed. Comparative Example 6-4, in which the same decorative film as in Comparative Example 6-3 was used and molding was performed 40 seconds after the end of the springback phenomenon, was achieved by lengthening the heating time for three-dimensional decorative molding. Adhesiveness was exhibited, but the added hindered amine light stabilizer volatilized, resulting in inferior weather resistance compared to Example 6-1. Comparative Example 6-5, in which the MFR (A) is 0.5 g/10 minutes or less and the layer (II) contains an ultraviolet absorber, increases the heating time of the three-dimensional decorative molding, and the adhesiveness is Although it was developed, the added ultraviolet absorber volatilized, and the weather resistance was inferior to that of Example 6-5.

The decorative film of the present invention and the method for producing a decorated molded article using the same can be used for a three-dimensional decorated molded article and its production.

1 decorative film 2 layer (II)
3 sealing layer (I)
4 Surface decoration layer (III)
5 Resin molding (decoration target, substrate)
6 decorative molding 11 upper chamber box 12 lower chamber box 13 jig 14 table 15 heater

Claims (16)

A decorative film containing a hindered amine-based light stabilizer and/or an ultraviolet absorber to be adhered onto a resin molding by thermoforming, the decorative film containing a polypropylene-based resin (A) Including a layer (II) containing a sealing layer (I) and a polypropylene resin (B),
The surface layer of the decorative film contains a hindered amine light stabilizer and / or an ultraviolet absorber,
The polypropylene resin (A) satisfies the following requirements (a1), the polypropylene resin (B) satisfies the following requirements (b1),
The seal layer (I) contains a resin composition (X3) in which the weight ratio of the polypropylene resin (A) and the ethylene-α-olefin random copolymer (C) is 97:3 to 5:95,
The ethylene-α-olefin random copolymer (C) is a decorative film that satisfies the following requirements (c1) to (c3) .
(a1) Melt flow rate (230° C., 2.16 kg load) (MFR(A)) exceeds 0.5 g/10 minutes.
(b1) Melt flow rate (230° C., 2.16 kg load) (MFR(B)) and MFR(A) satisfy the relational expression (b-1).
MFR(B)<MFR(A) Formula (b-1)
(c1) Ethylene content [E(C)] is 65% by weight or more.
(c2) Density is 0.850 to 0.950 g/cm ³ .
(c3) Melt flow rate (230° C., 2.16 kg load) (MFR(C)) is 0.1 to 100 g/10 minutes. A decorative film containing a hindered amine-based light stabilizer and/or an ultraviolet absorber to be adhered onto a resin molding by thermoforming, the decorative film containing a polypropylene-based resin (A) Including a layer (II) containing a sealing layer (I) and a polypropylene resin (B),
The surface layer of the decorative film contains a hindered amine light stabilizer and / or an ultraviolet absorber,
The polypropylene resin (A) satisfies the following requirements (a1), the polypropylene resin (B) satisfies the following requirements (b1),
The seal layer (I) contains a resin composition (X4) in which the weight ratio of the polypropylene resin (A) and the thermoplastic elastomer (D) is 97:3 to 5:95,
The thermoplastic elastomer (D) is a decorative film satisfying the following requirements (d1) to (d4).
(a1) Melt flow rate (230° C., 2.16 kg load) (MFR(A)) exceeds 0.5 g/10 minutes.
(b1) Melt flow rate (230° C., 2.16 kg load) (MFR(B)) and MFR(A) satisfy the relational expression (b-1).
MFR(B)<MFR(A) Formula (b-1)
(d1) A thermoplastic elastomer containing at least one of propylene and butene as a main component.
(d2) Density is 0.850-0.950g/cm ³ is.
(d3) Melt flow rate (230° C., 2.16 kg load) (MFR(D)) is 0.1 to 100 g/10 minutes.
(d4) Tensile modulus is smaller than polypropylene resin (A). A decorative film containing a hindered amine-based light stabilizer and/or an ultraviolet absorber for adhering to a resin molding by thermoforming, the decorative film containing a polypropylene-based resin (A) Including a layer (II) containing a sealing layer (I) and a polypropylene resin (B),
The surface layer of the decorative film contains a hindered amine light stabilizer and / or an ultraviolet absorber,
The polypropylene resin (A) satisfies the following requirements (a1), the polypropylene resin (B) satisfies the following requirements (b1),
The seal layer (I) contains a resin composition (X5) in which the weight ratio of the polypropylene resin (A) and the thermoplastic resin (E) is 97:3 to 5:95,
A decorative film in which the thermoplastic resin (E) satisfies the following requirement (e1) and the resin composition (X5) satisfies the following requirement (x1).
(a1) Melt flow rate (230° C., 2.16 kg load) (MFR(A)) exceeds 0.5 g/10 minutes.
(b1) Melt flow rate (230° C., 2.16 kg load) (MFR(B)) and MFR(A) satisfy the relational expression (b-1).
MFR(B)<MFR(A) Formula (b-1)
(e1) contains at least one of an alicyclic hydrocarbon group and an aromatic hydrocarbon group;
(x1) The isothermal crystallization time (t(X5)) (seconds) of the resin composition (X5) obtained by a differential scanning calorimeter (DSC) satisfies the following formula (x-1).
t(X5)≧1.5×t(A) Expression (x−1)
(In the formula, t (A) represents the isothermal crystallization time (seconds) of the polypropylene resin (A) measured at a temperature 10° C. higher than the crystallization start temperature of the polypropylene resin (A), and t (X5) is It is the isothermal crystallization time (seconds) of the resin composition (X5) measured at a temperature 10°C higher than the crystallization start temperature of the polypropylene resin (A).) Any one of claims 1 to 3, wherein the polypropylene resin (A) further satisfies the following requirements (a2) to (a4), and the polypropylene resin (B) further satisfies the following requirement (b2). The decorative film described in .
(a2) Metallocene-catalyzed propylene polymer.
(a3) The melting peak temperature (Tm(A)) is less than 150°C.
(a4) The molecular weight distribution (Mw/Mn(A)) obtained by GPC measurement is 1.5 to 3.5.
(b2) The melting peak temperature (Tm(B)) and Tm(A) satisfy the relational expression (b-2).
Tm(B)>Tm(A) Formula (b-2) The polypropylene resin (A) further satisfies the following requirement (a5), and the polypropylene resin (B) further satisfies the following requirement (b3), The additive according to any one of claims 1 to 4. decorative film.
(a5) The crystallization temperature (Tc(A)) is less than 100°C.
(b3) The crystallization temperature (Tc(B)) and Tc(A) satisfy the relational expression (b-3).
Tc(B)>Tc(A) Formula (b-3) The decorative film according to any one of claims 1 to 5 , wherein the polypropylene resin (A) is a propylene-ethylene block copolymer (F) satisfying the following requirements (f1) and (f2).
(f1) a melting peak temperature (Tm(F)) of 110 to 170°C;
(f2) 5 to 97% by weight of the component (F1) consisting of a propylene homopolymer or a propylene-ethylene random copolymer, and a component (F1) consisting of a propylene-ethylene random copolymer having a higher ethylene content than the component (F1) F2) is contained in an amount of 3 to 95% by weight. The decorative film according to any one of claims 1 to 5 , wherein the polypropylene resin (A) is a propylene-α-olefin copolymer. The decorative film according to claim 4 , wherein the Tm(A) is 140°C or less. 2. The decorative film according to claim 1 , wherein the ethylene-α-olefin random copolymer (C) further satisfies at least one of the following requirements (c4) and (c5).
(c4) Melting peak temperature (Tm(C)) is 30 to 130°C.
(c5) A random copolymer of ethylene and an α-olefin having 3 to 20 carbon atoms. The thermoplastic elastomer (D) is a propylene-ethylene copolymer with an ethylene content of less than 50 wt%, a butene-ethylene copolymer with an ethylene content of less than 50 wt%, and a propylene-ethylene-butene with an ethylene content of less than 50 wt%. 3. The decorative film according to claim 2 , which is at least one copolymer selected from the group consisting of copolymers, propylene-butene copolymers, and butene homopolymers. The decorative film according to claim 2 or 10 , wherein the thermoplastic elastomer (D) further satisfies the following requirement (d5).
(d5) The melting peak temperature (Tm(D)) is 30 to 170°C. The decorative film according to claim 3 , wherein the thermoplastic resin (E) is a styrene elastomer. The decorative film according to claim 3 , wherein the thermoplastic resin (E) is an alicyclic hydrocarbon resin. 7. The decorative film according to claim 6 , wherein the propylene-ethylene block copolymer (F) further satisfies at least one of the following requirements (f3) to (f5).
(f3) The ethylene content in the propylene-ethylene block copolymer (F) is 0.15 to 85% by weight.
(f4) The ethylene content of component (F1) is in the range of 0 to 6% by weight.
(f5) The ethylene content of component (F2) is in the range of 5 to 90% by weight. Preparing the decorative film according to any one of claims 1 to 14,
preparing a resin molded body;
setting the resin molded body and the decorative film in a decompressible chamber box;
depressurizing the inside of the chamber box;
a step of heating and softening the decorative film;
A method for manufacturing a decorated molded product, comprising: pressing the decorative film against the resin molded product; 16. The method for producing a decorative molded article according to claim 15 , wherein the resin molded article is made of a propylene-based resin composition.

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