WO2012157500A1 - 積層フィルムおよび成型体 - Google Patents
積層フィルムおよび成型体 Download PDFInfo
- Publication number
- WO2012157500A1 WO2012157500A1 PCT/JP2012/061942 JP2012061942W WO2012157500A1 WO 2012157500 A1 WO2012157500 A1 WO 2012157500A1 JP 2012061942 W JP2012061942 W JP 2012061942W WO 2012157500 A1 WO2012157500 A1 WO 2012157500A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- laminated film
- mass
- film
- less
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4063—Mixtures of compounds of group C08G18/62 with other macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
- C08G18/4269—Lactones
- C08G18/4277—Caprolactone and/or substituted caprolactone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6295—Polymers of silicium containing compounds having carbon-to-carbon double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/7806—Nitrogen containing -N-C=0 groups
- C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
- C08G18/7831—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing biuret groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
- G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
- G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
- G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/762—Self-repairing, self-healing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2457/00—Electrical equipment
- B32B2457/20—Displays, e.g. liquid crystal displays, plasma displays
- B32B2457/208—Touch screens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2483/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2483/04—Polysiloxanes
Definitions
- the present invention relates to a laminated film.
- the present invention particularly relates to a laminated film which is excellent in molding followability and scratch resistance as a molding material and is advantageous in terms of productivity and cost.
- a molding material such as decorative molding is provided with a surface hardness layer to prevent scratches during molding and to prevent scratches in the process of using the article after molding.
- the surface-hardened layer does not have enough elongation to follow the molding, and therefore cracks occur during molding. In extreme cases, the film breaks and the surface hardened layer peels off. For this reason, means such as forming a surface hardened layer after molding, or completely curing by heating or energy ray irradiation after molding in a semi-cured state is applied.
- JP 2009-84395 A Japanese Patent Laid-Open No. 2004-35599 JP 2006-137780 A International Publication No. WO2011 / 136042 Pamphlet
- Patent Document 1 has a problem that it has a high surface hardness but does not have self-healing properties and is not suitable for molding applications with a high molding magnification because of its low elongation.
- the energy ray curable materials described in Patent Documents 2 and 3 and the thermosetting material described in Patent Document 4 have sufficient self-healing properties, but dioctyl phthalate derived from a PVC sheet, cosmetics, oily magic, etc. In some cases, contamination was not observed in terms of contamination resistance.
- An object of the present invention is to provide a laminated film having a self-healing layer that is excellent in followability during molding and self-healing property and excellent in stain resistance.
- the present invention is a laminated film having an A layer on at least one side of a base film,
- the A layer has (1) (poly) caprolactone segment, and (2) urethane bond,
- the contact angle of distilled water on the A layer is 95 ° or more and less than 120 °, and the contact angle of diiodomethane on the A layer is 70 ° or more and less than 87 °.
- the laminated film of the present invention has excellent followability in warm molding, has a surface flaw repair function (self-healing), and has excellent contamination resistance.
- the laminated film of the present invention is particularly effective for a resin film in which surface scratches are likely to occur.
- the resin constituting the base film may be either a thermoplastic resin or a thermosetting resin, may be a homo resin, or may be a copolymer or a blend of two or more. More preferably, the resin constituting the base film is a thermoplastic resin because of good moldability.
- thermoplastic resins examples include polyolefin resins such as polyethylene, polypropylene, polystyrene, and polymethylpentene, alicyclic polyolefin resins, polyamide resins such as nylon 6 and nylon 66, aramid resins, polyester resins, polycarbonate resins, and polyarylate resins.
- Fluorine resins such as polyacetal resin, polyphenylene sulfide resin, tetrafluoroethylene resin, trifluoroethylene resin, trifluoroethylene chloride resin, tetrafluoroethylene-6 fluoropropylene copolymer, vinylidene fluoride resin, acrylic Resins, methacrylic resins, polyacetal resins, polyglycolic acid resins, polylactic acid resins, and the like can be used.
- the thermoplastic resin is preferably a resin having sufficient stretchability and followability.
- the thermoplastic resin is more preferably a polyester resin from the viewpoint of strength, heat resistance, and transparency.
- the polyester resin in the present invention is a general term for polymers having an ester bond as a main bond chain, and is obtained by polycondensation of an acid component and its ester with a diol component.
- Specific examples include polyethylene terephthalate, polypropylene terephthalate, polyethylene-2,6-naphthalate, polybutylene terephthalate, and the like. These may be copolymerized with other dicarboxylic acids and their esters or diol components as acid components or diol components.
- polyethylene terephthalate and polyethylene-2,6-naphthalate are particularly preferable in terms of transparency, dimensional stability, heat resistance and the like.
- additives such as an antioxidant, an antistatic agent, a crystal nucleating agent, an inorganic particle, an organic particle, a thinning agent, a heat stabilizer, a lubricant, an infrared absorber, an ultraviolet absorber, A dopant for adjusting the refractive index may be added.
- the base film may be either a single-layer base film or a laminated base film.
- polyester base film when resin which comprises a base film contains 50 mass% or more and 100 mass% or less of polyester resins in 100 mass% of all the components of a base film, a base film is called polyester base film.
- the polyester resin constituting the polyester base film has an intrinsic viscosity (measured in o-chlorophenol at 25 ° C. according to JIS K7367 (2000)) of 0.4 to 1.2 dl / g. 0.5 to 0.8 dl / g is particularly preferable.
- the polyester base film can be any of an unstretched (non-oriented) film, a uniaxially stretched (uniaxially oriented) film, and a biaxially stretched (biaxially oriented) film, but is biaxially stretched with excellent dimensional stability and heat resistance. It is preferable to use a film.
- the biaxially stretched film is preferably highly crystallized.
- the biaxial orientation refers to a material that exhibits a biaxial orientation pattern by wide-angle X-ray diffraction.
- the polyester base film may be a polyester film having fine cavities inside.
- the polyester base film may have a single layer structure or a laminated structure.
- polyester base film has a laminated structure
- different polyester resins preferably a layer (C layer) containing 50% by mass to 100% by mass of polyester resin C and 50% by mass to 100% by mass of polyester resin D are included.
- the layer (D layer) to be included is laminated.
- the different polyester resin means a polyester resin having a different molecular structure or a case where some components of the copolymer polyester resin are different.
- polyester base film has a laminated structure
- a layer (C layer) containing 50% by mass or more and 100% by mass or less of polyester resin C and 50% by mass or more and 100% by mass of polyester resin D different from polyester resin C are used.
- % Layer (D layer) is laminated.
- it has 50 or more layers including the C layer and the D layer.
- the number of stacked layers is more preferably 200 layers or more.
- the upper limit of the number of layers is preferably 1500 layers or less in consideration of a decrease in wavelength selectivity accompanying a decrease in stacking accuracy due to an increase in the size of the device or an increase in the number of layers.
- a polyester base film having a multilayer laminated structure is preferable because it has an interference color or further a metal color.
- the polyester resin C is preferably polyethylene terephthalate or polyethylene naphthalate
- the polyester resin D is preferably a polyester containing spiroglycol.
- the polyester containing spiroglycol is a copolyester copolymerized with spiroglycol (polyester whose glycol component is partly spiroglycol), or a homopolyester (a homopolyester whose glycol component is all spiroglycol), or those Refers to blended polyester. Polyesters containing spiroglycol are preferred because they have a small glass transition temperature difference from polyethylene terephthalate or polyethylene naphthalate, and are therefore difficult to be overstretched during molding and are difficult to delaminate.
- the polyester resin C is polyethylene terephthalate or polyethylene naphthalate
- the polyester resin D is a polyester containing spiroglycol and cyclohexanedicarboxylic acid.
- the polyester in which the polyester resin D contains spiroglycol and cyclohexanedicarboxylic acid is a polyester copolymerized with spiroglycol and cyclohexanedicarboxylic acid (or an ester derivative of cyclohexanedicarboxylic acid), or a homopolyester (the glycol component is all spiroglycol, A homopolyester in which all carboxylic acid components are cyclohexanedicarboxylic acid) or a polyester blended with this.
- the polyester resin D is a polyester containing spiroglycol and cyclohexanedicarboxylic acid
- a difference in in-plane refractive index from polyethylene terephthalate or polyethylene naphthalate is increased, and thus high reflectance is easily obtained.
- the glass transition temperature difference with polyethylene terephthalate or polyethylene naphthalate is small, it is difficult to be over-stretched during molding, and delamination is difficult.
- the polyester resin C is preferably polyethylene terephthalate or polyethylene naphthalate
- the polyester resin D is preferably a polyester containing cyclohexanedimethanol.
- the polyester containing cyclohexanedimethanol refers to a copolyester obtained by copolymerizing cyclohexanedimethanol, or a homopolyester (a homopolyester in which all glycol components are cyclohexanedimethanol), or a polyester obtained by blending them.
- Polyesters containing cyclohexanedimethanol are preferred because they have a small glass transition temperature difference from polyethylene terephthalate or polyethylene naphthalate, and are therefore less likely to be overstretched during molding and are also difficult to delaminate.
- the polyester resin D is more preferably an ethylene terephthalate polycondensate having a copolymerization amount of cyclohexanedimethanol of 15 mol% or more and 60 mol% or less.
- the polyester resin D is an ethylene terephthalate polycondensate having a copolymerization amount of cyclohexanedimethanol of 15 mol% or more and 60 mol% or less, a change in optical characteristics due to heating or aging is particularly small while having high reflection performance, Peeling does not easily occur between layers.
- the ethylene terephthalate polycondensate having a copolymerization amount of cyclohexanedimethanol of 15 mol% or more and 60 mol% or less shows very strong compatibility with polyethylene terephthalate.
- the cyclohexanedimethanol group has a cis or trans isomer as a geometric isomer, and a chair type or a boat type as a conformational isomer. The optical characteristics change little due to thermal history, and it is difficult to shake during film formation.
- the in-plane average refractive index of the C layer is preferably relatively higher than the in-plane average refractive index of the D layer.
- the difference between the in-plane average refractive index of the C layer and the in-plane average refractive index of the D layer is preferably 0.01 or more, and the thickness of one layer is preferably 0.03 ⁇ m or more and 0.5 ⁇ m or less. More preferably, the difference between the in-plane average refractive index of the C layer and the in-plane average refractive index of the D layer is 0.05 or more, and more preferably 0.1 or more.
- the film When the difference between the in-plane average refractive index of the C layer and the in-plane average refractive index of the D layer is 0.01 or more, the film exhibits excellent metal toning due to interference reflection. Further, when the difference between the in-plane average refractive index and the thickness direction refractive index of the C layer is 0.01 or more, and the difference between the in-plane average refractive index and the thickness direction refractive index of the D layer is 0.01 or less, the incident angle Even if becomes large, the reflectance in the reflection band does not decrease, which is more preferable.
- the glass transition temperature difference between the polyester resin C and the polyester resin D is preferably 20 ° C. or less.
- the thickness when the polyester base film in which the C layer and the D layer are laminated is formed becomes uniform, and the base film is used. Even when the laminated film is molded, cracks and peeling do not occur.
- the laminated film of the present invention is a laminated film having an A layer on at least one side of the base film, and the A layer has (1) a (poly) caprolactone segment and (2) a urethane bond, It is a laminated film in which the contact angle of distilled water on the A layer is 95 ° or more and less than 120 °, and the contact angle of diiodomethane on the A layer is 70 ° or more and less than 87 °.
- the laminated film of the present invention has an effect excellent in self-healing property and stain resistance by having the A layer on at least one side of the base film.
- the A layer exists only on one side of the base film in consideration of cost, although it depends on the use. In many applications, the A layer exists only on one side of the base film, and the laminated film has sufficient self-healing property and stain resistance.
- the A layer has (1) (poly) caprolactone segments.
- the elastic recovery property self-healing property
- the (poly) caprolactone segment refers to a segment represented by the following chemical formula 1.
- the A layer can have a (poly) caprolactone segment by forming the A layer using a composition containing a resin containing a (poly) caprolactone segment.
- the resin containing a (poly) caprolactone segment preferably has at least one hydroxyl group (hydroxyl group). The hydroxyl group is preferably at the end of the resin containing the (poly) caprolactone segment.
- the layer A can have a self-healing property because the layer A has a component having a (poly) caprolactone segment. That is, even if the surface of the A layer is scratched, the scratch can be extinguished (self-healed) in a short time of several seconds.
- (poly) caprolactone having a bi- to trifunctional hydroxyl group is particularly preferable. Specifically, (poly) caprolactone diol,
- Radical polymerizable caprolactone such as can be used.
- the resin containing the (poly) caprolactone segment may contain (or copolymerize) other segments and monomers in addition to the (poly) caprolactone segment.
- a polydimethylsiloxane segment or a polysiloxane segment may be contained (or copolymerized).
- the weight average molecular weight of the (poly) caprolactone segment in the resin containing the (poly) caprolactone segment is preferably 500 to 2500, and more preferably 1000 to 1500.
- the weight average molecular weight of the (poly) caprolactone segment is 500 to 2500, the self-healing effect is further exhibited and the scratch resistance is further improved.
- the (poly) caprolactone segment is copolymerized or added separately, in the 100% by mass of the total components of the composition used to form the A layer, the (poly) caprolactone segment An amount of 5 to 70% by mass is preferable in terms of self-healing properties and stain resistance.
- 100% by mass of all the components of the composition does not include a solvent that does not participate in the reaction.
- the monomer component involved in the reaction is included.
- the A layer has (2) a urethane bond.
- the A layer can have a urethane bond. Further, when forming the A layer, the A layer can also have a urethane bond by reacting an isocyanate group and a hydroxyl group to form a urethane bond.
- the A layer preferably has a urethane bond by reacting an isocyanate group with a hydroxyl group to form a urethane bond.
- the toughness of the A layer can be improved and the elastic recovery property (self-healing property) can be improved.
- the compound containing an isocyanate group means a resin containing an isocyanate group, or a monomer or oligomer containing an isocyanate group.
- the compound containing an isocyanate group include methylene bis-4-cyclohexyl isocyanate, trimethylolpropane adduct of tolylene diisocyanate, trimethylolpropane adduct of hexamethylene diisocyanate, trimethylolpropane adduct of isophorone diisocyanate, and tolylene diisocyanate.
- Polyisocyanates such as isocyanurate bodies, isocyanurate bodies of hexamethylene diisocyanate, burette bodies of hexamethylene isocyanate, and block bodies of the above isocyanates can be mentioned.
- aliphatic isocyanates are preferred because of their high self-healing properties compared to alicyclic and aromatic isocyanates.
- the compound containing an isocyanate group is more preferably hexamethylene diisocyanate.
- the isocyanate group-containing compound is particularly preferably an isocyanate having an isocyanurate ring from the viewpoint of heat resistance, and most preferably an isocyanurate of hexamethylene diisocyanate.
- An isocyanate having an isocyanurate ring forms a layer A having both self-healing properties and heat resistance.
- the A layer of the present invention is preferably formed by a heat reaction that generates a urethane bond with an isocyanate group and a hydroxyl group. If the isocyanate functional group of the compound containing an isocyanate group is 2 or more, it is preferable that the compound is more connected to the compound having a hydroxyl group to improve physical properties.
- 11 mass% or more and 40 mass% or less of the compound containing an isocyanate group are included in 100 mass% of all the components of the composition used in order to form A layer. preferable. However, 100% by mass of all the components of the composition used for forming the A layer does not include a solvent that does not participate in the reaction. The monomer component involved in the reaction is included.
- melamine crosslinking agents such as alkoxymethylol melamine, acid anhydride crosslinking agents such as 3-methyl-hexahydrophthalic anhydride, amine crosslinking agents such as diethylaminopropylamine, etc.
- Other crosslinkers can also be included.
- a crosslinking catalyst such as dibutyltin dilaurate or dibutyltin diethylhexoate may be used to promote the urethane bond formation reaction.
- the A layer preferably contains a resin having all of (1) (poly) caprolactone segment, (2) urethane bond, (3) polysiloxane segment and / or polydimethylsiloxane segment.
- the (A) layer is formed by including all of (1) (poly) caprolactone segment, (2) urethane bond, (3) polysiloxane segment and / or polydimethylsiloxane segment in one resin which is a polymer. Is preferable because it becomes a tougher layer.
- a composition containing at least three components of a polydimethylsiloxane copolymer having a hydroxyl group, (poly) caprolactone, and an isocyanate group-containing compound is applied onto a base film and reacted by heating to obtain (poly)
- a layer having a resin having all of caprolactone segment, polydimethylsiloxane segment and urethane bond can be obtained.
- the A layer is composed of (1) (poly) caprolactone segment, (2) urethane bond, (3) (poly) siloxane segment and / or (poly) dimethylsiloxane segment. It is more preferable to occupy 80 mass% or more and 100 mass% or less of resin which has this.
- the resin having all of (poly) caprolactone segment, polysiloxane segment and / or polydimethylsiloxane segment and urethane bond accounts for 80% by mass or more and 100% by mass or less. , Self-healing is increased.
- the A layer preferably has (3) a polysiloxane segment.
- the polysiloxane segment refers to a segment represented by the following chemical formula.
- R is any one of OH and an alkyl group having 1 to 8 carbon atoms, and has at least one of each in the formula.
- the composition used for forming the A layer can include a resin containing the polysiloxane segment.
- a partial hydrolyzate of a silane compound containing a hydrolyzable silyl group, an organosilica sol or a composition obtained by adding a hydrolyzable silane compound having a radical polymer to the organosilica sol contains a polysiloxane segment. It can be used as a resin.
- Resins containing polysiloxane segments are tetraalkoxysilane, methyltrialkoxysilane, dimethyldialkoxysilane, ⁇ -glycidoxypropyltrialkoxysilane, ⁇ -glycidoxypropylalkyldialkoxysilane, ⁇ -methacryloxypropyltri
- the resin containing a polysiloxane segment may contain (copolymerize) other segments in addition to the polysiloxane segment.
- a monomer component having a (poly) caprolactone segment and a polydimethylsiloxane segment may be contained (copolymerized).
- a monomer having a hydroxyl group that reacts with an isocyanate group is copolymerized as a resin containing a polysiloxane segment.
- a resin having a hydroxyl group that reacts with an isocyanate group is copolymerized with a resin containing a polysiloxane segment, the toughness of the A layer is improved.
- a layer A is formed using a composition containing a resin containing a hydroxyl group-containing polysiloxane segment (copolymer) and a compound containing an isocyanate group.
- A is formed, an A layer having a polysiloxane segment and a urethane bond can be efficiently formed.
- the polysiloxane segment is 1 to 20% by mass in 100% by mass of the total components of the composition used to form the A layer. % Is preferable in terms of self-healing property, stain resistance, weather resistance, and heat resistance. 100% by mass of the total components of the composition does not include a solvent that does not participate in the reaction. The monomer component involved in the reaction is included.
- the A layer preferably has (3) a polydimethylsiloxane segment.
- the polydimethylsiloxane segment refers to a segment represented by the following formula.
- the polydimethylsiloxane segment is present on the surface of the A layer.
- the lubricity of the surface of the A layer is improved and the frictional resistance can be reduced. As a result, scratchability can be suppressed.
- the composition used for forming the A layer can include a resin containing the polydimethylsiloxane segment.
- the resin containing a polydimethylsiloxane segment it is preferable to use a copolymer obtained by copolymerizing a vinyl monomer with a polydimethylsiloxane segment.
- the resin containing a polydimethylsiloxane segment is preferably copolymerized with a monomer having a hydroxyl group that reacts with an isocyanate group.
- a composition containing a resin containing a hydroxyl group-containing polydimethylsiloxane segment (copolymer) and a compound containing an isocyanate group is used.
- the resin containing the polydimethylsiloxane segment When the resin containing the polydimethylsiloxane segment is a copolymer with a vinyl monomer, it may be a block copolymer, a graft copolymer, or a random copolymer. When the resin containing the polydimethylsiloxane segment is a copolymer with a vinyl monomer, this is referred to as a polydimethylsiloxane copolymer.
- Polydimethylsiloxane copolymers can be produced by the living polymerization method, polymer initiator method, polymer chain transfer method, etc., but considering the productivity, the polymer initiator method, polymer chain transfer method can be used. It is preferable to use it.
- a two-stage polymerization is carried out by synthesizing a prepolymer in which a peroxide group is introduced into the side chain by copolymerizing a peroxy monomer and polydimethylsiloxane having an unsaturated group at a low temperature, and then copolymerizing the prepolymer with a vinyl monomer. Can also be done.
- a block copolymer can be synthesized by copolymerization.
- a graft copolymer can be easily obtained by copolymerizing a compound shown in the following, that is, a methacrylic ester of polydimethylsiloxane and a vinyl monomer.
- Examples of the vinyl monomer used in the copolymer with polydimethylsiloxane include methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, octyl acrylate, cyclohexyl acrylate, tetrahydrofurfuryl acrylate, methyl methacrylate, ethyl methacrylate, n -Butyl methacrylate, isobutyl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, lauryl methacrylate, methyl vinyl ether, ethyl vinyl ether, n-propyl vinyl ether, styrene, ⁇ -methyl styrene, acrylonitrile, methacrylonitrile, vinyl acetate, vinyl chloride, vinylidene chloride , Vinyl fluoride, vinylidene fluoride, glycidy
- Polydimethylsiloxane copolymers include aromatic hydrocarbon solvents such as toluene and xylene, ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone, ester solvents such as ethyl acetate and butyl acetate, ethanol, isopropyl alcohol, etc. It is preferable that the alcoholic solvent is produced by a solution polymerization method alone or in a mixed solvent.
- a polymerization initiator such as benzoyl peroxide or azobisisobutylnitrile is used in combination.
- the polymerization reaction is preferably carried out at 50 to 150 ° C. for 3 to 12 hours.
- the amount of the polydimethylsiloxane segment in the polydimethylsiloxane copolymer in the present invention is 1 to 30 in 100% by mass of all the components of the polydimethylsiloxane copolymer from the viewpoint of lubricity and contamination resistance of the A layer. It is preferable that it is mass%.
- the weight average molecular weight of the polydimethylsiloxane segment is preferably 1000-30000.
- the dimethylsiloxane segment is 1 to 20 in 100% by mass of the total components of the composition used to form the A layer.
- the mass% is preferable in terms of self-healing property, contamination resistance, weather resistance, and heat resistance. 100% by mass of the total components of the composition does not include a solvent that does not participate in the reaction. The monomer component involved in the reaction is included.
- a resin containing a polydimethylsiloxane segment when used as the composition used to form the A layer, other segments are contained (copolymerized) in addition to the polydimethylsiloxane segment. Also good.
- a (poly) caprolactone segment or a polysiloxane segment may be contained (copolymerized).
- the composition used to form the A layer includes a copolymer of (poly) caprolactone segment and polydimethylsiloxane segment, a copolymer of (poly) caprolactone segment and polysiloxane segment, (poly) caprolactone segment and poly A copolymer of a dimethylsiloxane segment and a polysiloxane segment can be used.
- the A layer obtained using such a composition can have a (poly) caprolactone segment and a polydimethylsiloxane segment and / or a polysiloxane segment.
- the reaction of the polydimethylsiloxane-based copolymer, (poly) caprolactone, and polysiloxane in the composition used to form the layer A having (poly) caprolactone segment, polysiloxane segment, and polydimethylsiloxane segment is When synthesizing the dimethylsiloxane-based copolymer, a (poly) caprolactone segment and a polysiloxane segment can be appropriately added and copolymerized.
- a layer contains the component (henceforth a fluorine compound A origin component) derived from the following fluorine compounds A.
- the A layer can impart stain resistance to the A layer.
- the fluorinated compound A refers to a compound represented by the following general formula (1).
- BR 1 -R f General formula (1) (B in the above general formula represents a reactive site or a hydroxyl group, R 1 represents an alkylene group having 1 to 3 carbon atoms and an ester structure derived therefrom, R f represents a fluoroalkyl group, You may have chains in the structure.)
- the reactive site of B means a site having a functional group that chemically reacts with radicals generated by receiving energy such as light or heat, or a hydroxyl group.
- the site having a functional group that chemically reacts with radicals generated by receiving energy such as light or heat include a vinyl group, an allyl group, an acryloyl group, and a methacryloyl group.
- B since the A layer has a urethane bond, B may be a hydroxyl group.
- the fluoroalkyl group is a substituent in which all hydrogens in the alkyl group are replaced with fluorine, and is a substituent composed of only a fluorine atom and a carbon atom.
- fluorine compound A examples include 2- (perfluorobutyl) ethanol, 2- (perfluorohexyl) ethanol, 2- (perfluorobutyl) ethyl acrylate, 2- (perfluorohexyl) ethyl acrylate, 2- (perfluorohexyl) ethyl acrylate, Fluorobutyl) ethyl methacrylate, 2- (perfluorohexyl) ethyl methacrylate, perfluorohexylethylene, 3- (perfluorohexyl) propylene and the like can be mentioned.
- fluorine compounds A when B is an acryloyl group, contamination resistance is particularly high and preferable.
- the fluorine compound A in which B contains an acryloyl group is more preferably 2- (perfluorohexyl) ethyl acrylate.
- the A layer obtained using the composition can contain a component derived from the fluorine compound A.
- the fluorine compound A-derived component is contained in 100% by mass of all components of the composition used for forming the A layer.
- the component derived from the fluorine compound A is 0.5% by mass or more and 25% by mass or less in 100% by mass of all the components of the A layer of the obtained laminated film.
- the self-healing property and contamination resistance of the A layer can be made particularly excellent. That is, while maintaining excellent self-healing property, even if dioctyl phthalate derived from a PVC sheet or cosmetics adheres to the surface of the A layer, it can be removed cleanly by wiping.
- the fluorine compound A when the fluorine compound A is contained in the composition used for forming the A layer, in addition to the fluorine compound A, other fluorine compounds may be contained.
- examples of such compounds include hexafluoropropylene, hexafluoropropylene oxide, perfluoro (propyl vinyl ether), perfluorohexyl iodide, 2,2-bis (4-hydroxyphenyl) hexafluoropropane, and the like. May be.
- the composition used for forming the A layer preferably contains an initiator, a curing agent, and a catalyst. An initiator and a catalyst are used to accelerate the curing of the fluorine compound A.
- the initiator those capable of initiating or accelerating polymerization, condensation or cross-linking reaction of the coating composition by anion, cation, radical reaction or the like are preferable.
- initiators, curing agents and catalysts can be used.
- the initiator, the curing agent, and the catalyst may be used alone, or a plurality of initiators, curing agents, and catalysts may be used at the same time.
- acidic catalysts include aqueous hydrochloric acid, formic acid, acetic acid and the like.
- thermal polymerization initiator include peroxides and azo compounds.
- the photopolymerization initiator include alkylphenone compounds, sulfur-containing compounds, acylphosphine oxide compounds, amine compounds, and the like.
- alkylphenone compound is preferable from the viewpoint of curability.
- alkylphenone type compounds include 1-hydroxy-cyclohexyl-phenyl-ketone, 2.2-dimethoxy-1.2-diphenylethane-1-one, 2-methyl-1- (4-methylthiophenyl)- 2-morpholinopropan-1-one, 2-benzyl-2-dimethylamino-1- (4-phenyl) -1-butane, 2- (dimethylamino) -2-[(4-methylphenyl) methyl]- 1- (4-phenyl) -1-butane, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -1-butane, 2- (dimethylamino) -2-[(4-methylphenyl ) Methyl] -1- [4- (4-morpholinyl) phenyl] -1-butane, 1-cyclohexyl-
- the content ratio of the initiator and the curing agent in the composition used for forming the A layer is preferably 0.001 to 30 parts by mass with respect to 100 parts by mass of the fluorine compound A. More preferably, it is 0.05 mass part to 20 mass parts, More preferably, it is 0.1 mass part to 10 mass parts.
- the A layer of the present invention may contain other components such as an acrylic segment, a polyolefin segment, and a polyester segment.
- the polyolefin segment is a polymer composed of repeating units derived from an olefin having 2 to 20 carbon atoms having a structure equivalent to that of a polyolefin resin.
- the acrylic segment is a polymer containing an acrylic unit as a constituent component, and preferably contains 50 mol% or more of the acrylic unit.
- Preferable examples include methyl methacrylate unit, acrylmethyl unit, acrylethyl unit and acrylbutyl unit. If the A layer has an acrylic segment, the A layer can be made excellent in stain resistance and toughness.
- diol component of the polyester segment in addition to butanediol and / or hexanediol, ethylene glycol, 1,3-propanediol, neopentyl glycol, 2-methyl 1,3-propanediol, 1,4-cyclohexanedimethanol, Polytetramethylene glycol, polyethylene glycol, polypropylene glycol, dimer diol, and hydrogenated dimer diol can be used.
- polyester segment As the acid component of the polyester segment, terephthalic acid, naphthalenedicarboxylic acid, isophthalic acid, sebacic acid, adipic acid, azelaic acid, succinic acid, hexahydroterephthalic acid, and the like can be used, and a plurality of these components are included. May be.
- a heat-resistant agent for example, a heat-resistant agent, an ultraviolet absorber, a light stabilizer, organic and inorganic particles, a pigment, a dye, a release agent, and an antistatic agent can be added to the A layer.
- the glass transition temperature (Tg) of the A layer is preferably ⁇ 30 ° C. or higher and 15 ° C. or lower.
- the glass transition temperature (Tg) of the A layer is more preferably 0 ° C. or higher and 15 ° C. or lower.
- the glass transition temperature of the A layer is ⁇ 30 ° C. or higher and 15 ° C. or lower, the self-healing rate is greatly improved, and a self-healing property is maintained even in a low temperature region.
- the glass transition temperature of layer A exceeds 15 ° C, self-healing at an ambient temperature of 10 ° C or less becomes extremely slow, and when the glass transition temperature of layer A is less than -30 ° C, slipperiness decreases. This causes problems such as winding failure on the roll, blocking, and molding defects.
- the glass transition temperature of the A layer is 0 ° C. or higher and 15 ° C. or lower, the self-healing property at the atmospheric temperature of 5 ° C. is good and the contamination resistance is good.
- the compound containing an isocyanate group is contained in an amount of 11 to 40% by mass in 100% by mass of all the components of the composition used for forming the A layer. % Is preferable.
- the A layer preferably has a low glass transition temperature component.
- the A layer preferably has an acrylic segment having a low glass transition temperature component.
- the acrylic segment having a low glass transition temperature component is a segment composed of a polymer of monomers such as n-butyl acrylate, isobutyl acrylate, n-butyl methacrylate, and isobutyl methacrylate. It is preferable because the glass transition temperature of the A layer can be controlled to ⁇ 30 ° C. or more and 15 ° C. or less by changing the content of the acrylic segment of the low glass transition temperature component in the A layer.
- the laminated film of the present invention preferably has a wound recovery time of 25 seconds or less at a temperature of 10 ° C. of the A layer. More preferably, the scratch recovery time at a temperature of 10 ° C. of the A layer is 10 seconds or less. When the recovery time is 25 seconds or less, the self-healing speed is greatly improved. A recovery time of 10 seconds or less is preferable because even if the molding magnification is increased, the decrease in self-healing property is small.
- the laminated film of the present invention has a different recovery time depending on the temperature. It has been found that the lower the temperature, the longer the recovery time and the higher the temperature, the shorter the recovery time.
- the laminated film of the present invention has a slightly different recovery time depending on the base film. It is known that the recovery time is shortened if the base film is the laminated configuration, and the recovery time is prolonged if the single-layer configuration is, but the change is 1 second or less when the temperature of the A layer is 10 ° C. The contribution to recovery time is negligible.
- the glass transition temperature of the A layer is preferably ⁇ 30 ° C. or higher and 15 ° C. or lower.
- Contamination resistance can be made particularly excellent by setting the number of fluorine atoms to 0.4% or more and 50% or less on the surface of the A layer side. Regarding the surface of the A layer side, the number of fluorine atoms is set to 0.4% or more and 50% or less. % Or less is preferable.
- the laminated film of the present invention has a TOF-SIMS in the range of 1% or more and 100% or less in thickness from the A layer side surface of the laminated film toward the base film direction.
- the maximum value of the fluorine atom detection intensity by TOF-SIMS in the range from 0% to less than 1% in the thickness from the A layer side surface of the laminated film to the base film direction.
- a / b is preferably 0% or more and 60% or less, more preferably 5% or more and 25% or less.
- a means one point showing the maximum value among the detected intensities of a plurality of fluorine atoms detected in this range. The same applies to b.
- a / b is more preferably 5% or more and 20% or less.
- the said fluorine compound A (component derived from a fluorine compound) has the characteristics which gather on the surface and harden
- the layer A of the laminated film of the present invention preferably contains a component derived from the fluorine compound A.
- the layer A was obtained through the laminating step, the heating step, and the aging step described below without containing the component derived from the fluorine compound A.
- the surface properties greatly depend on the fluorine compound A-derived component, Although contamination resistance is obtained, self-healing property cannot be obtained.
- the A layer is a layer having a fluorine compound A-derived component and a (poly) caprolactone segment, etc., rather than two or more layers in which a layer made of the fluorine compound A is laminated on a layer having a (poly) caprolactone segment or the like.
- An embodiment consisting of only one layer is preferred.
- the A layer itself having (1) (poly) caprolactone segment and (2) urethane bond contains a component derived from the fluorine compound A.
- only one layer means a layer in which there is no interface having a luminance difference of 5% or more inside. Details will be described later.
- the number of layers is preferably one, when producing the laminated film of the present invention, only the composition containing the fluorine compound A is used as a composition for forming the A layer. It is preferable to apply and cure. When the composition containing the fluorine compound A is applied to the base film and cured, the fluorine compound A moves to the surface of the layer A, so it is composed of one layer, and there is a concentration distribution among the contained components in the layer.
- the laminated film of the present invention can be obtained. That is, the laminated film of the present invention is preferably a laminated film obtained by curing the composition used for forming the A layer containing the fluorine compound A, after coating the substrate film only once. .
- the contact angle on the A layer of distilled water is 95 ° or more and less than 120 °
- the contact angle on the A layer of diiodomethane is 70 ° or more and less than 87 °. .
- the contact angle on the A layer of distilled water is more preferably 105 ° or more and less than 120 °, and still more preferably 95 ° or more and less than 120 °. Further, the contact angle of the diiodomethane on the A layer is more preferably 75 ° or more and less than 87 °, and further preferably 80 ° or more and less than 87 °.
- Contamination resistance refers to resistance to dioctyl phthalate and the like derived from creams, oil-based magic, and vinyl chloride sheets having a skin-beautifying effect and an ultraviolet blocking effect.
- the component derived from the fluorine compound A is contained in an amount of 0.5 to 25% by mass.
- the A layer is laminated to form an A1 layer having (1) (poly) caprolactone segments and (2) urethane bonds on the base film, and then the A1 layer It is also possible to form an A2 layer having a contact angle with distilled water of 95 ° or more and less than 120 ° and a contact angle with diiodomethane of 70 ° or more and less than 87 °.
- A1 layer having (1) (poly) caprolactone segments and (2) urethane bonds on the base film
- A1 layer It is also possible to form an A2 layer having a contact angle with distilled water of 95 ° or more and less than 120 ° and a contact angle with diiodomethane of 70 ° or more and less than 87 °.
- the laminated film of this invention obtained by making the composition used in order to form A layer containing the fluorine compound A apply
- the contact angle of diiodomethane on the A layer to 80 ° or more and less than 87 ° it is more important to manufacture under special conditions. That is, in order to control the contact angle of the diiodomethane on the A layer to 80 ° or more and less than 87 °, it is important to collect fluorine atoms on the surface. In order to make the contact angle on the A layer of diiodomethane 70 ° or more and less than 87 °, it is possible to simply form the A layer using a composition containing the fluorine compound A, but the contact angle is 80 °. In order to control the angle to be less than 87 °, it is required to further collect fluorine atoms on the surface.
- the fluorine compound A in the coating liquid moves to the surface of the A layer. It is effective to reduce the movement resistance until it is done. For that purpose, it is effective to suppress the hardening of the material forming the A layer other than the fluorine compound A.
- a high boiling point solvent for example, cyclohexanone or butyl acetate
- a low boiling point solvent for example, methyl ethyl ketone or ethyl acetate
- the low boiling point solvent is preferably a solvent having a boiling point of 80 ° C. or lower, more preferably 75 ° C. or higher and 80 ° C. or lower.
- the high boiling point solvent is preferably a solvent having a boiling point of 125 ° C. or higher, more preferably 125 ° C. or higher and 160 ° C. or lower.
- the mass ratio of these solvents is preferably 1 to 50:99 to 50 for high boiling point solvent: low boiling point solvent.
- the oxygen concentration in the process be 2% by volume or less by performing the process in a nitrogen atmosphere because the curing of the fluorine compound A is not inhibited by oxygen.
- the fluorine compound A is preferably cured by irradiation with energy rays, and the other materials for forming the A layer are preferably cured by heat. That is, the step of applying the composition used to form the A layer containing the fluorine compound A only once on the base film, the energy ray irradiation step, the heating step described later, and the aging step described later It is preferable to form A layer by carrying out in order. By performing these operations, the contact angle of diiodomethane on the A layer can be set to 80 ° or more and less than 87 °, which is preferable.
- the thickness of the A layer is preferably 15 to 30 ⁇ m in order to obtain a laminated film having good self-healing properties and cosmetic resistance.
- the thickness of the A layer is preferably 15 to 30 ⁇ m in order to obtain a laminated film having good self-healing properties and cosmetic resistance.
- the thickness of the A layer is reduced by molding, it is effective to increase the thickness of the A layer in accordance with the molding magnification.
- the thickness of the A layer preferred for molding at a molding magnification of 1.1 times is 16.5 to 33 ⁇ m, and the thickness of the A layer preferred for molding at a molding magnification of 1.6 times is 24 to 48 ⁇ m.
- the average breaking elongation at 80 ° C. and 150 ° C. of the A layer of the laminated film of the present invention is preferably 65% or more and less than 100%, more preferably 70% or more and less than 100%.
- the average breaking elongation at 80 ° C. and 150 ° C. is 65% or more, sufficient elongation can be maintained, and when it is less than 100%, the followability with the base film is good.
- the layer A of the laminated film of the present invention can be produced, for example, through the following steps in that order.
- Laminating step (1) (poly) caprolactone segment, (3) polysiloxane segment and / or polydimethylsiloxane segment, (2) urethane bond, fluorine compound A layer (A layer) on at least one side of the base film Are stacked.
- Lamination of the A layer to the base film includes, for example, a method of applying a composition used to form the A layer and, if necessary, a coating liquid containing a solvent to at least one side of the base film. Can do.
- a known coating method such as a gravure coating method, a micro gravure coating method, a die coating method, a reverse coating method, a knife coating method, or a bar coating method can be applied.
- Heating step By heating, the solvent in the layer volatilizes, and the crosslinking reaction between the isocyanate group in the composition used for forming the A layer and other segments can be promoted.
- the remaining amount of isocyanate groups in the A layer before the aging step is preferably 10% or less, more preferably 5% or less, based on the amount of isocyanate groups before the heating step. More preferably, it is substantially 0%. Substantially 0% means that an isocyanate group is not detected even when infrared spectrophotometric analysis is performed.
- the isocyanate group in the A layer reacts with moisture in the air to form a urea bond, and the A layer after the aging process becomes hard. This causes the average fracture elongation of the A layer to decrease. Therefore, it is desirable that the isocyanate group reaction is allowed to proceed as much as possible (more preferably) before the aging step. When the reaction is insufficient, tackiness remains in the A layer, and when it is wound into a roll, blocking with the opposite surface occurs, and it may be difficult to peel off after aging.
- the heating temperature in the heating step is preferably 60 ° C or higher, more preferably 80 ° C or higher. Considering the generation of wrinkles due to heat shrinkage of the base film, the heating temperature is preferably 180 ° C. or less, and considering the volatilization of the fluorine compound A by heating, it is preferably 160 ° C. or less, more preferably It is preferable that it is 100 degrees C or less. When the heating temperature is 60 ° C. or higher, the solvent is sufficiently volatilized.
- the heating time is 1 minute or longer, preferably 2 minutes or longer, more preferably 3 minutes or longer. From the viewpoint of maintaining productivity, dimensional stability of the base film, and transparency, the heating time is desirably 5 minutes or less.
- the heating temperature is preferably 60 ° C. or more and 160 ° C. or less, and the heating time is preferably 1 minute or more and 5 minutes or less.
- the heating method in the heating step is preferably performed with hot air from the viewpoint of heating efficiency, and a known hot air dryer or a hot air furnace capable of continuous conveyance such as roll conveyance or floating can be applied.
- Fluorine compound A in the composition used for forming the A layer can be cured by irradiating energy rays.
- Curing with energy rays is preferably electron beams (EB rays) or ultraviolet rays (UV rays) from the viewpoint of versatility.
- the oxygen concentration is preferably 2% by volume or less, more preferably 0% by volume because oxygen inhibition can be prevented, and therefore, under a nitrogen atmosphere (nitrogen purge). It is preferable to cure.
- the oxygen concentration is as high as 18% by volume or more, the curing of the outermost surface is inhibited, the curing becomes insufficient, and the self-healing property and the stain resistance may be insufficient.
- Examples of the ultraviolet lamp used when irradiating ultraviolet rays include a discharge lamp method, a flash method, a laser method, and an electrodeless lamp method.
- Case of UV cured using a high pressure mercury lamp is a discharge lamp type, illuminance of ultraviolet rays is 100 mW / cm 2 or more 3000 mW / cm 2 or less.
- Illuminance of ultraviolet is preferably 200 mW / cm 2 or more 2000 mW / cm 2 or less, more preferably 300 mW / cm 2 or more 1500 mW / cm 2 or less.
- Integrated quantity of ultraviolet light is 100 mJ / cm 2 or more 3000 mJ / cm 2 or less.
- Integrated light quantity is preferably from 200 mJ / cm 2 or more 2000 mJ / cm 2 or less, more preferably 300 mJ / cm 2 or more 1500 mJ / cm 2 or less.
- the ultraviolet illuminance is the irradiation intensity received per unit area, and varies depending on the lamp output, the emission spectrum efficiency, the diameter of the light emitting bulb, the design of the reflecting mirror, and the light source distance to the irradiated object. However, the illuminance does not change depending on the conveyance speed. Further, the UV integrated light amount is irradiation energy received per unit area, and is the total amount of photons reaching the surface.
- the integrated light quantity is inversely proportional to the irradiation speed passing under the light source, and is proportional to the number of irradiations and the number of lamps.
- the drying step and the curing step may be performed simultaneously.
- the heated laminated film is preferably subjected to an aging treatment after passing through the energy ray irradiation step.
- the aging temperature is preferably 20 to 60 ° C., and more preferably 40 to 60 ° C.
- the aging time is preferably 3 days or more, more preferably 7 days or more, and still more preferably 20 days or more. Since the urethane bond is increased by the aging treatment and the average breaking elongation of the A layer can be 65% or more and less than 100%, it is preferable that the curing of the A layer is completed by the aging process.
- the aging treatment is preferably carried out by a single wafer or a roll in a temperature-controlled room where a predetermined temperature can be set.
- the preferred use of the laminated film of the present invention is a molding application, particularly a decorative molding application applied to a housing such as a personal computer or a mobile phone.
- the laminated film of the present invention can be made into a molded body by applying a molding method such as injection molding, pressure molding, vacuum molding, thermoforming, press molding or the like.
- the present invention can be particularly suitably applied to uses that are heated to 80 ° C. to 180 ° C. during molding.
- the molding magnification of the laminated film of the present invention is preferably 1.1 to 1.6 times.
- the molding ratio is particularly likely to be high at the bent portion and the curved portion, and it is preferable that the molding ratio at the bent portion and the curved portion is 1.1 to 1.6 times because it can be used for deep drawing. .
- the laminated film of the present invention can also be suitably used as a touch panel comprising the laminated film.
- the characteristic measurement method and effect evaluation method in the present invention are as follows.
- a layer thickness and layer thickness Cross sections of the laminated film and the molded film are obtained by cutting with a diamond knife of a microtome (manufactured by Nippon Microtome, RMS-50) (referred to as method A.
- a sample obtained by method A is referred to as sample A). After that, it is left to stand in a 1% by mass osmium tetroxide solution (4 ° C.) for 2 hours.
- a sample is obtained by washing three times with 100 ml of ethanol having a purity of 99.8% by mass or more for 20 minutes while shaking (referred to as method B.
- the sample obtained by method B is referred to as sample B).
- sample C another sample having the same operation is prepared using a 1% by mass ruthenium tetroxide solution (referred to as method C.
- the sample obtained by method C is referred to as sample C).
- sample C an image magnified up to 40,000 times according to the layer thickness observed with a transmission electron microscope (H-7100FA manufactured by Hitachi, Ltd.) was obtained, and the highest contrast was obtained. The method by which samples were obtained was selected.
- the layer thickness was measured about the sample of the selected specific method. The measurement was an average value of 10 samples in the selected method. Moreover, the measurement part cut out 50mm square of the center part of a sample, and measured three places in it.
- Number of layers The number of layers is measured by examining the luminance of the image used for measuring the layer thickness using image analysis software Image-Pro Plus manufactured by Nippon Roper. And the brightness
- the structure is composed of two or more layers.
- Shall be when measuring the brightness of the layer laminated on the base film, it is not possible to find an interface with a brightness difference of 5% or more in the direction substantially parallel to the base film, and it is composed of one layer. Shall be.
- the layer is composed of one layer.
- the layer having a thickness of less than 0.01 nm is ignored.
- the average fracture elongation of the A layer at 150 ° C. was determined in the same manner as in the case where the measurement atmosphere temperature was 80 ° C., except that the measurement atmosphere temperature was 150 ° C.
- TOF-SIMS Time-of-flight secondary ion mass spectrometry: TOF-SIMS
- Light source LuminalAce LA-150UX ring light installed at the camera tip
- Camera VW-6000 (Keyence Corporation) sample rate: 10pps exposure time: 20000 ⁇ s.
- Tg of layer A It was measured and calculated according to JIS-K-7122 (1987) using differential calorimetry (DSC). The sample of layer A that was cut out with a blade knife was packed in an aluminum pan and heated from -100 ° C. to 100 ° C. at a rate of 20 ° C./min.
- PVC sheet Stain resistance (PVC sheet) Achilles Co., Ltd.
- PVC sheet “Achilles type C + clear blue tint” is cut into a 4cm square and placed in the center on a sample cut into a 5cm square, and a 500g load is applied evenly under an atmosphere with a temperature of 40 ° C and a relative humidity of 95%. Leave for 6 hours, remove the sample and wipe the surface clean with gauze. The state of the surface was observed and judged according to the following criteria.
- Film size 100mm x
- 100mm Clip pressure 5MPa
- Preheating / stretching temperature 100 ° C
- Fan air volume 50%
- Preheating time 40 seconds
- Stretching speed 20% / sec.
- a raw material A1 having a solid content concentration of 40% by mass was prepared.
- Example 1 A solvent prepared by adding 10 parts by mass of 2- (perfluorohexyl) ethyl acrylate and 0.5 parts by mass of 1-hydroxy-cyclohexyl-phenyl-ketone to raw material A1, and mixing methylethylketone and cyclohexanone in a mass ratio of 93: 7.
- the solid content concentration is adjusted again to 30% by mass, and the layer A thickness after the aging process is 30 ⁇ m on a 100 ⁇ m thick polyester base film (manufactured by Toray Industries, Inc., “Lumirror” U46). It applied using a wire bar. After the application, it was heated with a hot air dryer at 100 ° C. for 2 minutes (heating step).
- Table 1 shows the evaluation results of the obtained laminated film and molded film. Excellent self-healing properties and excellent stain resistance.
- Example 2 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the thickness of the A layer and the ratio of molding stretching were changed.
- Example 2 stretching at the time of molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the A layer thickness after the aging process was 23 ⁇ m.
- Example 3 stretching at the time of molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the A layer thickness after the aging step was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- Example 4 A laminated film and a molded film were obtained in the same manner as in Example 1 except that 10 parts by mass of 2- (perfluorobutyl) ethyl methacrylate was added instead of 10 parts by mass of 2- (perfluorohexyl) ethyl acrylate. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 5 A laminated film and a molded film were obtained in the same manner as in Example 4 except that the thickness of the A layer and the ratio of molding stretching were changed.
- Example 5 stretching during molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the thickness of the A layer after the aging process was 23 ⁇ m.
- Example 6 stretching at the time of molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the thickness of the A layer after the aging process was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- Example 7 A laminated film and a molded film were obtained in the same manner as in Example 1 except that 10 parts by mass of 2- (perfluorohexyl) ethyl methacrylate was added instead of 10 parts by mass of 2- (perfluorohexyl) ethyl acrylate. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 8 A laminated film and a molded film were obtained in the same manner as in Example 7 except that the thickness of the A layer and the ratio of molding stretching were changed.
- stretching at the time of molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the A layer thickness after the aging step was 23 ⁇ m.
- stretching at the time of molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the A layer thickness after the aging step was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- Example 10 10 parts by mass of 2- (perfluorohexyl) ethanol was added to the raw material A1, and the thickness of the A layer after the aging process was 30 ⁇ m on a 100 ⁇ m thick polyester base film (“Lumirror” U46, manufactured by Toray Industries, Inc.). It applied so that it might become, using a wire bar. After the application, it was heated with a hot air dryer at 160 ° C. for 2 minutes (heating step). Thereafter, heating (aging) was performed at 40 ° C. for 14 days (aging process) to obtain a laminated film. Next, the obtained film was molded. At this time, only preheating was performed without stretching. The obtained results are shown in Table 1.
- Table 1 shows the evaluation results of the obtained film (described as film) and the molded film. Excellent self-healing properties and excellent stain resistance.
- Example 11 to 12 A laminated film and a molded film were obtained in the same manner as in Example 10 except that the thickness of the A layer and the ratio of molding stretching were changed.
- Example 11 stretching at the time of molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the thickness of the A layer after the aging process was 23 ⁇ m.
- Example 12 stretching at the time of molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the A layer thickness after the aging step was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- Example 13 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the addition amount of 2- (perfluorohexyl) ethyl acrylate was changed to 3 parts by mass. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 14 A laminated film and a molded film were obtained in the same manner as in Example 13 except that the thickness of the A layer and the ratio of molding stretching were changed.
- Example 14 stretching at the time of molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the thickness of the A layer after the aging process was 23 ⁇ m.
- Example 15 stretching at the time of molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the A layer thickness after the aging step was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- Example 16 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the addition amount of 2- (perfluorohexyl) ethyl acrylate was 20 parts by mass. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 17 A laminated film and a molded film were obtained in the same manner as in Example 16 except that the thickness of the A layer and the ratio of molding stretching were changed.
- stretching at the time of molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the A layer thickness after the aging step was 23 ⁇ m.
- stretching during molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the thickness of the A layer after the aging process was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- Example 19 A laminated film was obtained using the raw material A2 under the same conditions as in Example 1. Next, the obtained film was molded in the same manner as in Example 1. Table 1 shows the evaluation results of the obtained film and molded film. Excellent self-healing property even at low temperatures.
- Example 20 A laminated film and a molded film were obtained in the same manner as in Example 19 except that the thickness of the A layer and the ratio of molding stretching were changed.
- Example 20 stretching at the time of molding was performed at a magnification of 1.2 times in the vertical direction and 1.2 times in the horizontal direction so that the A layer thickness after the aging step was 23 ⁇ m.
- Example 21 stretching at the time of molding was performed at a magnification of 1.3 times in the vertical direction and 1.3 times in the horizontal direction so that the A layer thickness after the aging step was 19 ⁇ m.
- Table 1 Even if the thickness of the A layer was reduced, it exhibited excellent self-healing properties and excellent stain resistance. Also, no molding defects were found.
- PET Polyethylene terephthalate
- PET Polyethylene terephthalate
- cyclohexane polyethylene terephthalate copolymer having an intrinsic viscosity of 0.72
- PET obtained by copolymerizing 30 mol% of dicarboxylic acid and 20 mol% of spiroglycol component with 0.1 mass% of “Adeka Stub” AS36 (manufactured by ADEKA) as an antioxidant was used.
- Polyyester resin C and polyester resin D are alternately laminated by slit plate 1 having 267 slits, slit plate 2 having 269 slits, and slit plate 3 having 267 slits while weighing to 2/1. And it was made to merge by a feed block, and it was set as the laminated body laminated
- the polyester resin A has 400 layers and the polyester resin B has 401 layers. It was set as the structure laminated
- the slit shape was designed so that the layer thicknesses of the adjacent C layer and D layer were substantially the same. In this design, a reflection band exists between 350 nm and 1200 nm.
- the laminated body composed of the total of 801 layers thus obtained was supplied to the multi-manifold die, and further, a layer made of the polyester resin A supplied from another extruder was formed on the surface layer, and then molded into a sheet shape. It was rapidly cooled and solidified on a casting drum maintained at a surface temperature of 25 ° C. by electrostatic application.
- the flow path shape and the total discharge amount were set so that the time from when the polyester resin C and the polyester resin D merged to when rapidly solidified on the casting drum was about 8 minutes.
- the obtained cast film was heated with a roll group set at 75 ° C., and then stretched 3.0 times in the longitudinal direction while rapidly heating from both sides of the film with a radiation heater between 100 mm in the stretch section length. Cooled down. Next, this uniaxially stretched film was led to a tenter, preheated with hot air at 100 ° C., and stretched 3.3 times in the transverse direction at a temperature of 110 ° C. The stretched film was directly heat-treated in a tenter with hot air of 235 ° C., then subjected to a relaxation treatment of 5% in the width direction at the same temperature, and then gradually cooled to room temperature and wound up. The thickness of the obtained film was 100 ⁇ m. The obtained film was free from delamination and had an excellent gloss tone.
- a layer A was formed on this film in the same manner as in Example 1 to obtain a laminated film and a molded film.
- the obtained results are shown in Table 1.
- the resulting film and molded film had excellent metallic appearance and self-healing properties.
- Example 23 Copolymerized polyester (Eastster PETG6763 manufactured by Eastman Chemical Co., Ltd.) obtained by copolymerizing 1,4-cyclohexanedimethanol component with 33 mol% of glycol component, and PET with an intrinsic viscosity of 0.65 and a melting point of 255 ° C. F20S] was mixed at a mass ratio of 76:24. The mixture was melt kneaded at 280 ° C. using a vented twin screw extruder.
- 1,4-cyclohexanedimethanol 25 mol% copolymerized polyethylene terephthalate resin in which 2 mol% of the by-produced diethylene glycol was copolymerized with respect to the glycol component in the resin was obtained.
- PET [Toray F20S] having an intrinsic viscosity of 0.65 and a melting point of 255 ° C. and 1,4-cyclohexanedimethanol 25 mol% copolymerized polyethylene terephthalate resin (diethylene glycol copolymerization rate 2 mol%) were mixed at a mass ratio of 70:30. .
- the mixture was dried at 180 ° C. for 4 hours in a vacuum dryer, and after sufficiently removing moisture, supplied to a single screw extruder, melted at 275 ° C., removed foreign matter, and leveled the amount of extrusion,
- the sheet was discharged from a T-die onto a cooling drum whose temperature was controlled at 25 ° C. At that time, a wire-like electrode having a diameter of 0.1 mm was applied electrostatically and adhered to the cooling drum to obtain an unstretched film.
- the film temperature is raised with a heating roll, and the preheating temperature is set to 9
- the film was stretched 3.2 times in the longitudinal direction at 0 ° C. and a stretching temperature of 95 ° C., and immediately cooled with a metal roll whose temperature was controlled at 40 ° C.
- the film was stretched 3.5 times in the width direction at a preheating temperature of 90 ° C. and a stretching temperature of 100 ° C. with a tenter-type transverse stretching machine, and the temperature was maintained at 210 ° C. for 5 seconds while relaxing 4% in the width direction.
- Heat treatment was performed to obtain a biaxially oriented polyester film having a film thickness of 188 ⁇ m.
- the obtained biaxially oriented polyester film was very excellent in transparency and moldability although it was slightly weak in scratch resistance.
- a layer A was formed on this biaxially oriented polyester film in the same manner as in Example 1 to obtain a laminated film and a molded film.
- the obtained results are shown in Table 1.
- the obtained film and molded film were excellent in self-healing properties.
- Example 24 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the temperature in the heating step was 160 ° C. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 25 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the solid content concentration was 40% by mass. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 26 A laminated film and a molded film were obtained in the same manner as in Example 25 except that the temperature in the heating step was 160 ° C. The obtained results are shown in Table 1. Excellent self-healing properties and excellent stain resistance.
- Example 27 A laminated film and a molded film were obtained in the same manner as in Example 1 except that methyl ethyl ketone was used for dilution of the raw material A1. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 28 A laminated film and a molded film were obtained in the same manner as in Example 27 except that the temperature in the heating step was 160 ° C. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 29 A laminated film and a molded film were obtained in the same manner as in Example 27 except that the solid content concentration was 40% by mass. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 30 A laminated film and a molded film were obtained in the same manner as in Example 28 except that the solid content concentration was 40% by mass. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 31 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the oxygen concentration in the energy ray irradiation step was 21% by volume. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 32 A laminated film and a molded film were obtained in the same manner as in Example 31 except that the temperature in the heating step was 160 ° C. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 33 A laminated film and a molded film were obtained in the same manner as in Example 31 except that the solid content concentration was 40% by mass. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 34 A laminated film and a molded film were obtained in the same manner as in Example 32 except that the solid content concentration was 40% by mass. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 35 A laminated film and a molded film were obtained in the same manner as in Example 31 except that methyl ethyl ketone was used for dilution of the raw material A1. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 36 A laminated film and a molded film were obtained in the same manner as in Example 35 except that the temperature in the heating step was 160 ° C. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 37 A laminated film and a molded film were obtained in the same manner as in Example 35 except that the solid content concentration was 40% by mass. The obtained results are shown in Table 1. Excellent self-healing property.
- Example 38 A laminated film and a molded film were obtained in the same manner as in Example 37 except that the temperature in the heating step was 160 ° C. The obtained results are shown in Table 1. Excellent self-healing property.
- polycaprolactone triol manufactured by Daicel Chemical Industries, Plaxel 308, molecular weight 850
- Plaxel 308 molecular weight 850
- 0.02 part by mass of dibutyltin laurate was added and 24 ° C. at 24 ° C.
- the mixture was held for a period of time, and 111 parts by mass of toluene was added to obtain a urethane acrylate having a solid content of 50% by mass.
- an active energy ray-curable composition was prepared by mixing 3 parts by mass of 1-hydroxy-cyclohexyl-phenyl-ketone with 100 parts by mass of this urethane acrylate.
- Example 39 A solvent in which 10 parts by mass of 2- (perfluorohexyl) ethyl acrylate and 0.5 parts by mass of 1-hydroxy-cyclohexyl-phenyl-ketone were added to the raw material A3, and methyl ethyl ketone and cyclohexanone were mixed at a mass ratio of 93: 7.
- the solid content concentration is adjusted again to 30% by mass, and the layer A thickness after the aging process is 30 ⁇ m on a 100 ⁇ m thick polyester base film (manufactured by Toray Industries, Inc., “Lumirror” U46). It applied using a wire bar. After the application, it was heated with a hot air dryer at 100 ° C.
- Table 1 shows the evaluation results of the obtained laminated film and molded film. Excellent self-healing properties and excellent stain resistance.
- Light Acrylate 3EG-A 3 parts by mass of stearyl acrylate (Nippon Yushi Co., Ltd., Bremer SA), 13 parts by mass of toluene and light
- An active energy ray-curable composition was prepared by mixing 3 parts by mass of an initiator (Irgacure 184 manufactured by Ciba Geigy).
- Example 40 A laminated film and a molded film were obtained in the same manner as in Example 39 except that the raw material A4 was used. The obtained results are shown in Table 1. Excellent self-healing property.
- Table 2 shows the evaluation results of the obtained film (described as film) and the molded film. Although excellent self-healing property was exhibited, the contamination resistance was insufficient.
- Example 4 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the amount of 2- (perfluorohexyl) ethyl acrylate added was 0.1 parts by mass. The obtained results are shown in Table 2. Although excellent self-healing property was exhibited, the contamination resistance was insufficient.
- Example 5 A laminated film and a molded film were obtained in the same manner as in Example 1 except that the amount of 2- (perfluorohexyl) ethyl acrylate was changed to 30 parts by mass. The obtained results are shown in Table 2. Although self-healing was insufficient, it showed excellent contamination resistance.
- Example 6 A laminated film and a molded film were obtained in the same manner as in Example 10 except that the amount of 2- (perfluorohexyl) ethanol added was 0.1 parts by mass. The obtained results are shown in Table 2. Although excellent self-healing property was exhibited, the contamination resistance was insufficient.
- Example 7 A laminated film and a molded film were obtained in the same manner as in Example 10 except that the amount of 2- (perfluorohexyl) ethanol added was changed to 30 parts by mass. The obtained results are shown in Table 2. Although self-healing was insufficient, it showed excellent contamination resistance.
- Comparative Example 8 A composition containing 5 parts by mass of 1-hydroxy-cyclohexyl-phenyl-ketone is diluted with methyl ethyl ketone to 100 parts by mass of 2- (perfluorohexyl) ethyl acrylate to prepare a coating solution having a solid content concentration of 40% by mass. And this was apply
- Table 2 shows the evaluation results of the obtained film (described as a laminated film) and the molded film. Although it did not show self-healing, it showed excellent stain resistance.
- Example 9 A laminated film and a molded film were obtained in the same manner as in Example 1 except that 10 parts by mass of hexafluoropropene trimer was added instead of 10 parts by mass of 2- (perfluorohexyl) ethyl acrylate. The obtained results are shown in Table 2. Although excellent self-healing property was exhibited, the contamination resistance was insufficient.
- the laminated film of the present invention can be used for applications where moldability and self-healing properties are required at the same time.
- it can be suitably used as a film for decorative molding applied particularly to a housing of a personal computer or a mobile phone.
- the laminated film of the present invention can be formed into a molded body by applying a molding method such as injection molding, pressure molding, vacuum molding, thermoforming, press molding or the like.
- the laminated film of the present invention can cope with deep drawing.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Theoretical Computer Science (AREA)
- Human Computer Interaction (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Laminated Bodies (AREA)
- Position Input By Displaying (AREA)
Abstract
Description
該A層が、(1)(ポリ)カプロラクトンセグメント、および(2)ウレタン結合、を有し、
蒸留水の該A層上での接触角が95°以上120°未満、ジヨードメタンの該A層上での接触角が70°以上87°未満であることを特徴とする、積層フィルムである。
本発明において基材フィルムを構成する樹脂は、熱可塑性樹脂、熱硬化性樹脂のいずれでもよく、ホモ樹脂であってもよく、共重合または2種類以上のブレンドであってもよい。より好ましくは、基材フィルムを構成する樹脂は、成型性が良好であるため、熱可塑性樹脂である。
本発明では、基材フィルムを構成する樹脂が、基材フィルムの全成分100質量%において、ポリエステル樹脂を50質量%以上100質量%以下含む場合、基材フィルムをポリエステル基材フィルムという。
以下、基材フィルムの少なくとも片側に、A層を有する積層フィルムについて説明する。
本発明では、A層が、(1)(ポリ)カプロラクトンセグメントを有する。A層が(ポリ)カプロラクトンセグメントを有することで、A層に弾性回復性(自己治癒性)を賦与することができる。
本発明では、A層が(2)ウレタン結合を有する。
本発明では、A層が(3)ポリシロキサンセグメントを有することが好ましい。本発明において、ポリシロキサンセグメントとは、以下の化学式で示されるセグメントを指す。なお、下記化学式5において、Rは、OHとC数1~8のアルキル基のいずれかであり、式中においてそれぞれを少なくとも1つ以上有する。
本発明では、A層が(3)ポリジメチルシロキサンセグメントを有することが好ましい。
本発明では、A層が、以下のフッ素化合物Aに由来する成分(以下、フッ素化合物A由来成分という)を含むことが好ましい。A層が、フッ素化合物A由来成分を含むことで、A層に耐汚染性を賦与することができる。
B-R1-Rf ・・・一般式(1)
(上記一般式中のBは反応性部位またはヒドロキシル基を示し、R1は炭素数1から3のアルキレン基およびそれらから導出されるエステル構造を示し、Rfはフルオロアルキル基を示し、それぞれ側鎖を構造中に持ってもよい。)
Bの反応性部位とは、光または熱などのエネルギーをうけて発生したラジカルなどにより化学反応する官能基を持つ部位、又は、ヒドロキシル基を意味する。光または熱などのエネルギーをうけて発生したラジカルなどにより化学反応する官能基を持つ部位の具体例としては、ビニル基、アリル基、アクリロイル基、メタクリロイル基などが挙げられる。また、本発明においてはA層がウレタン結合を有する為、Bがヒドロキシル基であってもよい。
<他の添加剤>
A層を形成するために用いる組成物には、開始剤や硬化剤や触媒を含むことが好ましい。開始剤および触媒は、フッ素化合物Aの硬化を促進するために用いられる。開始剤としては、塗料組成物をアニオン、カチオン、ラジカル反応等による重合、縮合または架橋反応を開始あるいは促進できるものが好ましい。
本発明のA層は、アクリルセグメント、ポリオレフィンセグメント、ポリエステルセグメントなどのその他の成分が含まれていても良い。
本発明の積層フィルムは、A層のガラス転移温度(Tg)が-30℃以上15℃以下であることが好ましい。A層のガラス転移温度(Tg)は、より好ましくは、0℃以上15℃以下である。
本発明の積層フィルムは、A層の温度10℃での傷の回復時間が25秒以下であることが好ましい。さらに好ましくは、A層の温度10℃での傷の回復時間が10秒以下である。回復時間が25秒以下であると、自己治癒速度が大きく向上する。また、回復時間が10秒以下であれば、成型倍率を高くしても自己治癒性の低下が少ないので、好ましい。なお、本発明の積層フィルムは温度によって回復時間が異なる。温度が低ければ回復時間が長くなり、温度が高ければ回復時間が短くなることがわかっている。また、本発明の積層フィルムは基材フィルムによって回復時間がわずかに異なる。基材フィルムが前記積層構成であれば回復時間が短くなり、前記単層構成であれば回復時間が長くなることがわかっているが、その変化はA層の温度10℃のとき1秒以下と回復時間への寄与はわずかである。
<フッ素原子の分布>
本発明の積層フィルムは、A層側表面について、XPSにより検出されるフッ素原子、炭素原子、窒素原子、酸素原子、ケイ素原子の合計数を100%とした際に、フッ素原子の数が0.4%以上50%以下であることが好ましく、10%以上50%以下であることがより好ましい。A層側表面について、フッ素原子の数を0.4%以上50%以下とすることで、耐汚染性を特に優れたものとすることができる。A層側表面について、フッ素原子の数を0.4%以上50%以下とする方法としては、A層の全成分100質量%中に、フッ素化合物A由来成分を0.5質量%以上25質量%以下含むことが好ましい。
<A層の層数>
本発明の積層フィルムは、基材フィルムの少なくとも片側に有する層がA層の一層のみからなることが好ましい。
本発明の積層フィルムは、蒸留水のA層上での接触角が95°以上120°未満であり、ジヨードメタンのA層上での接触角が70°以上87°未満であることが重要である。
本発明の積層フィルムのA層は、例えば、以下の工程をその順に経て、製造することができる。A層の80℃および150℃における平均破壊伸度を65%以上100%未満にするためには、積層工程、加熱工程、エネルギー線照射工程の後に、エージング工程を経ることが特に好ましい。
前記基材フィルムの少なくとも片側に、(1)(ポリ)カプロラクトンセグメント、(3)ポリシロキサンセグメント及び/またはポリジメチルシロキサンセグメント、(2)ウレタン結合、フッ素化合物Aを有する層(A層)を積層する。基材フィルムへのA層の積層は、例えば、A層を形成するために用いる組成物と、必要に応じて溶媒を含む塗液を、基材フィルムの少なくとも片側に、塗布する手法を挙げることができる。また、塗布方法としては、グラビアコート法、マイクログラビアコート法、ダイコート法、リバースコート法、ナイフコート法、バーコート法など公知の塗布方法を適用することができる。
加熱を行うことにより、層中の溶媒が揮発するとともに、A層を形成するために用いる組成物中のイソシアネート基と、他のセグメントとの架橋反応を促進することができる。本発明では、加熱工程後、エージング工程前のA層中のイソシアネート基の残量が、加熱工程前のイソシアネート基の量に対して、10%以下であることが好ましく、より好ましくは5%以下、更に好ましくは実質的に0%である。実質的に0%とは、赤外分光光度計分析を行ってもイソシアネート基が検出されないことを言う。A層中にイソシアネート基が多量に残存すると、その後のエージング工程において、A層中のイソシネート基が、空気中の水分と反応し、ウレア結合を形成し、エージング工程後のA層が硬質化して、A層の平均破壊伸度が低下する原因となる。そのためにエージング工程前に、イソシアネート基の反応をできるだけ進行(より好ましくは完了)させておくことが望ましい。反応が不十分である場合には、A層にタック性が残り、ロール状に巻き取った場合に反対面とのブロッキングが発生し、エージング後には剥離困難となる場合がある。
エネルギー線を照射する事により、A層を形成するために用いる組成物中のフッ素化合物Aを硬化させることができる。エネルギー線による硬化は、汎用性の点から電子線(EB線)または紫外線(UV線)が好ましい。また紫外線により硬化する場合は、酸素阻害を防ぐことができることから酸素濃度が2体積%以下であることが好ましく、より好ましくは0体積%であることが好ましいため、窒素雰囲気下(窒素パージ)で硬化するのが好ましい。酸素濃度が18体積%以上と高い場合には、最表面の硬化が阻害され、硬化が不十分となり、自己治癒性、耐汚染性が不十分となる場合がある。また、紫外線を照射する際に用いる紫外線ランプの種類としては、例えば、放電ランプ方式、フラッシュ方式、レーザー方式、無電極ランプ方式等が挙げられる。放電ランプ方式である高圧水銀灯を用いて紫外線硬化させる場合、紫外線の照度は100mW/cm2以上3000mW/cm2以下である。紫外線の照度は200mW/cm2以上2000mW/cm2以下が好ましく、300mW/cm2以上1500mW/cm2以下がさらに好ましい。紫外線の積算光量は100mJ/cm2以上3000mJ/cm2以下である。積算光量は200mJ/cm2以上2000mJ/cm2以下が好ましく、300mJ/cm2以上1500mJ/cm2以下がさらに好ましい。ここで、紫外線照度とは、単位面積当たりに受ける照射強度で、ランプ出力、発光スペクトル効率、発光バルブの直径、反射鏡の設計および被照射物との光源距離によって変化する。しかし、搬送スピードによって照度は変化しない。また、紫外線積算光量とは単位面積当たりに受ける照射エネルギーで、その表面に到達するフォトンの総量である。積算光量は、光源下を通過する照射速度に反比例し、照射回数とランプ灯数に比例する。硬化を熱により行う場合、乾燥工程と硬化工程とを同時におこなってもよい。
加熱工程において、加熱した積層フィルムは、エネルギー線照射工程を経た後、エージング処理を行うことが好ましい。エージング温度は、好ましくは、20~60℃であり、より好ましくは、40℃~60℃である。エージング時間は、好ましくは、3日間以上、より好ましくは、7日間以上、更に好ましくは、20日間以上である。エージング処理により、ウレタン結合が増え、A層の平均破壊伸度を65%以上100%未満とすることができる為、エージング工程によってA層の硬化が完了することが好ましい。エージング処理は、所定の温度設定が可能な恒温室で枚葉もしくはロールで行うことが好ましい。
本発明における特性の測定方法および効果の評価方法は以下のとおりである。
厚み:
積層フィルムおよび成型フィルムの断面を、ミクロトーム(日本ミクロトーム製、RMS-50)のダイヤモンドナイフにて切削して得る(方法Aとする。方法AによるサンプルをサンプルAという。)。この後、1質量%四酸化オスミウム液(4℃)中で2時間する放置する。純度99.8質量%以上のエタノール100mlにて3回、各20分揺り動かしながら洗浄を行い、サンプルを得る(方法Bとする。方法BによるサンプルをサンプルBという。)。また、1質量%四酸化ルテニウム液を用いて、同様の操作を行なった別のサンプルを作成する(方法Cとする。方法CによるサンプルをサンプルCという。)。これらのサンプルA,B,Cについて透過型電子顕微鏡(日立(株)製 H-7100FA)にて観察される層厚みに応じて最大4万倍まで拡大させた像を得て、最もコントラストの高いサンプルを得られる方法を選択した。
層数:
層数の測定は、層厚みの測定に用いた画像について、日本ローパー(株)製の画像解析ソフトImage-Pro Plusを用いて輝度を調べることで行なう。そして、基材フィルム上に積層される層の有する輝度を測定して、基材フィルムと略平行な方向に輝度の差が5%以上となる界面を設定できるか否かで判断する。
積層フィルムを10mm幅×200mm長に切り出し、長手方向にチャックで把持してインストロン型引っ張り試験機(インストロン社製超精密材料試験機MODEL5848)にて引っ張り速度100mm/分で伸長した。測定雰囲気温度を80℃とし、伸度1%単位でサンプルを採取した。採取したサンプルの薄膜断面を切り出し、観察するA層の厚みが、透過型電子顕微鏡の観察画面上において、30mm以上になるような倍率でA層を観察し、A層の平均厚みの50%以上のクラック(亀裂)が発生している場合をクラック有り(A層の破壊有り)として、当該フィルムの破壊伸度(80℃-1回目)とした。同一の測定を計3回行い、破壊伸度(80℃-1回目)、破壊伸度(80℃-2回目)および破壊伸度(80℃-3回目)を得て、それらの平均値を80℃におけるA層の平均破壊伸度とした。
アルバック・ファイ社製PHI5000 VersaProbeにて測定した。条件は以下の通り。
X線源:mono-Al
出力:24.2W
X線ビーム径:100μm
取り出し角:45°
パスエネルギー:23.50eV
各原子の組成比は、高分解能スペクトルからピーク面積を測定し、伝達関数修正された原子感度定数を適用することによって決定され、解析には付属のソフトウェアが使用される。
ION TOF社製TOF-SIMSVを用い、積層フィルムのA層側表面から基材フィルム方向に向かって、(1)の方法で求められた厚みについて、二次イオン質量分析法によってフッ素原子の検出強度を求めた。条件は以下の通り。
・Analysis parameter
Analysis beam:Bi+, negative
Current beam:1.000pA
Area:50×50μm2
・Sputter parameter
Sputter beam:Cs+,10keV
Current beam:39.000nA
Area:200×200μm2
表には、A層の全体厚みを100%とした際に、積層フィルムのA層側表面から基材フィルム方向に向かって厚さ1%以上100%以下の範囲における、TOF-SIMSによるフッ素原子の検出強度の最大値をa、積層フィルムのA層側表面から基材フィルム方向に向かって厚さ0%以上1%未満の範囲における、TOF-SIMSによるフッ素原子の検出強度の最大値をbとしたときの、a/b[%]を示した。この測定で検出限界よりも下回っている場合(フッ素原子が検出されない場合)は、表中で「‐」と示した。
JIS K5600(1999年制定)『引っ掻き硬度(鉛筆法)』に従って、塗膜表面に傷を形成した。条件は以下のとおり。
鉛筆:HB鉛筆(“ユニ”三菱鉛筆製)
荷重:750g
引っ掻き速度:10mm/s
サンプルの真上にハイスピードカメラを設置して、傷が入ってから画面上の傷の10秒後の輝度差が1.0%以下になるまでの時間を計測し、回復時間とした。回復時間が速ければそれだけ自己治癒性が高いことを表す。測定は3回行い、その平均値を採った。また、測定は温調されているアクリルボックス内で行い、温度5℃、10℃、20℃の時で行った。また、成型フィルムの測定個所は、フィルムの中心部分50mm四方を切り取り、その中の3箇所を測定した。カメラの撮影条件は以下のとおりである。
カメラ:VW-6000(キーエンス株式会社)
sample rate:10pps
exposhure time:20000μs 。
示差熱量分析(DSC)を用い、JIS-K-7122(1987年)に従って測定・算出した。刃ナイフで削りだしたA層のサンプルを、アルミ製のパンに詰め、-100℃から100℃まで20℃/minで昇温した。
装置:セイコー電子工業(株)製”ロボットDSC-RDC220”
データ解析”ディスクセッションSSC/5200”
サンプル質量:5mg。
温度25℃、相対湿度65%の雰囲気下で試料を24時間放置後、協和界面化学(株)製接触角計CA-D型を用いて、蒸留水、ナカライテスク(株)製ジヨードメタンを滴下後、10秒後の接触角をそれぞれ測定した。なお、各試料につき3回測定を行い、平均値を接触角とした。
5cm角に切り出した試料に花王(株)製”アトリックス ハンドクリーム”を0.5g塗布し、温度40℃、相対湿度95%の雰囲気下で6時間放置後、25℃相対湿度65%の雰囲気下で30分間放置し、表面をガーゼできれいに拭き取る。温度25℃、相対湿度65%の雰囲気下で24時間放置後、表面の状態を観察し、下記の基準に則り判定を行った。
○(優):白斑の発生なし。
●(良):白斑の発生がほとんどなし。
△(可):白斑が発生するが、拭き取ればきれいになる。
×(不可):白斑が発生する。拭き取っても温度25℃、相対湿度65%の雰囲気下で24時間放置後に再度発生する。
5cm角に切り出した試料にアキレス(株)製塩ビシート”アキレスタイプC+ 青味透明”を4cm角に切り出して中央に載せ、均等に500gの荷重を掛け温度40℃、相対湿度95%の雰囲気下で6時間放置し、試料を取り外し、表面をガーゼできれいに拭き取る。表面の状態を観察し、下記の基準に則り判定を行った。
○(優):外観の変化なし。
△(可):塩ビシートを載せた箇所にわずかな跡が発生。
×(不可):塩ビシートを載せた箇所に明確な跡が発生。
3室ストレッチャー(KARO IV、ブルックナー製)で、フィルムの端部をクリップにて把持し、以下の条件にて同時二軸延伸を行った。この時、クリップでのサンプルの外れを防止するために、サンプルの四辺を、幅10mm、厚み100μmのポリエチレンテレフタレートフィルムで挟んで補強している。本法による延伸は、実際の成型と同じ挙動で積層フィルムが延伸されるため、得られたフィルムは成型体(成型フィルム)とみなすことができる。なお、予熱のみで延伸をしていない場合においても、成型フィルムとする。成型時の延伸の倍率は、元の寸法に対して延伸後に何倍まで延伸されているかを示している。
クリップ圧力:5MPa
予熱・延伸温度:100℃
ファン風量:50%
予熱時間:40秒
延伸速度:20%/sec 。
積層フィルムおよび成型フィルムの断面を、ミクロトーム(日本ミクロトーム製、RMS-50)のダイヤモンドナイフにて切削し、白金で蒸着後、SEM(日立(株)製)にて、成型前と成型後のA層の厚みを測定し、下記の式から成型倍率を求めた。測定個所は成型フィルムの中心部分50mm四方を切り取り、その中の3箇所を測定した。成型倍率とは厚みの変化である為、前記した成型時の延伸の倍率とは異なる。
成型後、A層の状態を目視観察し、下記の基準に則り評価を行った。また、観察部分は、成型フィルムの中心部分50mm四方の中で行った。
○(良):クラックや剥離が発生せず、表面性に問題ない。
×(不良):クラックや剥離が生じて実用上問題がある。
<ポリシロキサン(a)の合成>
攪拌機、温度計、コンデンサ及び窒素ガス導入管を備えた500mlのフラスコにエタノール106質量部、メチルトリメトキシシラン270質量部、γ-メタクリロキシプロピルメチルジメトキシシラン23質量部、脱イオン水100質量部、1質量%塩酸1質量部及びハイドロキノンモノメチルエーテル0.1質量部を仕込み、80℃で3時間反応させ、ポリシロキサン(a)を合成した。これをメチルイソブチルケトンで50質量%に調整した。
ポリシロキサン(a)の合成と同様の装置を用い、トルエン50質量部、およびメチルイソブチルケトン50質量部、ポリジメチルシロキサン系高分子重合開始剤(和光純薬株式会社製、VPS-0501)20質量部、メタクリル酸メチル18質量部、メタクリル酸ブチル38質量部、2-ヒドロキシエチルメタクリレート23質量部、メタクリル酸1質量部および1-チオグリセリン0.5質量部を仕込み、180℃で8時間反応させてポリジメチルシロキサン系ブロック共重合体(a)を得た。得られたブロック共重合体は、固形分50質量%であった。
ポリジメチルシロキサン系ブロック共重合体(a)75質量部、上記のポリシロキサン(a)10質量部および水酸基を有するポリカプロラクトントリオール(ダイセル化学工業(株)製、プラクセル308、分子量850)15質量部を配合(混合)した混合物、100質量部に対し、ヘキサメチレンジイソシアネートのイソシアヌレート体(武田薬品工業(株)製、タケネートD-170N)を15質量部添加し、さらにメチルエチルケトンを用いて希釈し、固形分濃度40質量%の原料A1を作成した。
原料A1に2-(パーフルオロヘキシル)エチルアクリレートを10質量部、1-ヒドロキシ-シクロヘキシル-フェニル-ケトンを0.5質量部添加し、メチルエチルケトンとシクロヘキサノンを93:7の質量比率で混合した溶媒を用いて固形分濃度が30質量%となるように再度調整し、厚み100μmのポリエステル基材フィルム(東レ(株)製、“ルミラー”U46)上に、エージング工程後のA層厚みが30μmとなるようにワイヤーバーを用いて塗布した。塗布後、100℃で2分間、熱風乾燥機で加熱した(加熱工程)。その後、160W/cmの高圧水銀灯ランプ(アイグラフィックス(株)製)を用いて、照度600W/cm2、積算光量800mJ/cm2の紫外線を、酸素濃度0.1体積%の下で照射し(エネルギー線照射工程)、40℃で14日間加熱(エージング)を行い(エージング工程)、積層フィルムを得た。次に、この得られたフィルムの成型を行った。このとき延伸は行わずに予熱だけを行った。
A層の厚みと成型延伸の倍率を変更した以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。実施例2は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例3は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
2-(パーフルオロヘキシル)エチルアクリレート10質量部の代わりに2-(パーフルオロブチル)エチルメタクリレート10質量部を添加した以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
A層の厚みと成型延伸の倍率を変更した以外は、実施例4と同様にして積層フィルムと成型フィルムを得た。実施例5は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例6は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
2-(パーフルオロヘキシル)エチルアクリレート10質量部の代わりに2-(パーフルオロヘキシル)エチルメタクリレート10質量部を添加した以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
A層の厚みと成型延伸の倍率を変更した以外は、実施例7と同様にして積層フィルムと成型フィルムを得た。実施例8は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例9は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
原料A1に2-(パーフルオロヘキシル)エタノールを10質量部添加し、厚み100μmのポリエステル基材フィルム(東レ(株)製、“ルミラー”U46)上に、エージング工程後のA層厚みが30μmとなるようにワイヤーバーを用いて塗布した。塗布後、160℃で2分間、熱風乾燥機で加熱した(加熱工程)。その後、40℃で14日間加熱(エージング)を行い(エージング工程)、積層フィルムを得た。次に、この得られたフィルムの成型を行った。このとき延伸は行わずに予熱だけを行った。得られた結果を表1に示す。
A層の厚みと成型延伸の倍率を変更した以外は、実施例10と同様にして積層フィルムと成型フィルムを得た。実施例11は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例12は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
2-(パーフルオロヘキシル)エチルアクリレートの添加量を3質量部とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
A層の厚みと成型延伸の倍率を変更した以外は、実施例13と同様にして積層フィルムと成型フィルムを得た。実施例14は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例15は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
2-(パーフルオロヘキシル)エチルアクリレートの添加量を20質量部とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
A層の厚みと成型延伸の倍率を変更した以外は、実施例16と同様にして積層フィルムと成型フィルムを得た。実施例17は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例18は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
<原料A2の調合>
ポリジメチルシロキサン系ブロック共重合体(a)75質量部、ポリシロキサン(a)10質量部および水酸基を有するポリカプロラクトントリオール(ダイセル化学工業(株)製 プラクセル308、重量平均分子量850)15質量部を配合(混合)した混合物、100質量部に対し、ヘキサメチレンジイソシアネートのビウレット体(バイエル(株)製、デスモジュールN3200)を15質量部添加し、さらにメチルエチルケトンを用いて希釈し、固形分濃度40質量%の原料A2を作成した。
原料A2を、実施例1と同様の条件で、積層フィルムを得た。次に、実施例1と同様して、この得られたフィルムの成型を行った。得られたフィルムと成型フィルムの評価結果を表1に示す。低温でも優れた自己治癒性を示した。
A層の厚みと成型延伸の倍率を変更した以外は、実施例19と同様にして積層フィルムと成型フィルムを得た。実施例20は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。実施例21は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表1に示す。A層厚みを薄くしても優れた自己治癒性を示し、優れた耐汚染性を示した。また、成型不良も見られなかった。
ポリエステル樹脂Cとして、固有粘度0.65、融点255℃のポリエチレンテレフタレート(以下、PETとも表す)[東レ製F20S]を用い、ポリエステル樹脂Dとして固有粘度0.72のポリエチレンテレフタレートの共重合体(シクロヘキサンジカルボン酸30mol%、スピログリコール成分20mol%共重合したPET)に酸化防止剤である“アデカスタブ”AS36[ADEKA製]を0.1質量%添加したものを用いた。これらポリエステル樹脂Cおよびポリエステル樹脂Dは、それぞれ乾燥した後、別々の押出機に供給した。
1,4-シクロヘキサンジメタノール成分が、グリコール成分に対して、33mol%共重合された共重合ポリエステル(イーストマン・ケミカル社製 EatsterPETG6763)と、固有粘度0.65、融点255℃のPET[東レ製F20S]を質量比76:24で混合した。混合物を、ベント式二軸押出機を用いて、280℃で溶融混練した。この結果、副生したジエチレングリコールが、樹脂中のグリコール成分に対して、2モル%共重合された、1,4-シクロヘキサンジメタノール25mol%共重合ポリエチレンテレフタレート樹脂が得られた。これを、1,4-シクロヘキサンジメタノール25mol%共重合ポリエチレンテレフタレート樹脂(ジエチレングリコール共重合率2モル%)と記載する。
0℃、延伸温度を95℃で長手方向に3.2倍延伸し、すぐに40℃に温度制御した金属
ロールで冷却化した。
延伸し、そのままテンター内にて幅方向に4%のリラックスを掛けながら温度210℃で
5秒間の熱処理を行い、フィルム厚み188μmの二軸配向ポリエステルフィルムを得た。得られた二軸配向ポリエステルフィルムは、耐傷性がやや弱いものの透明性と成型性に非常に優れていた。
加熱工程における温度を160℃とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
固形分濃度を40質量%とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
加熱工程における温度を160℃とした以外は、実施例25と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示し、優れた耐汚染性を示した。
原料A1の希釈にメチルエチルケトンを用いた以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
加熱工程における温度を160℃とした以外は、実施例27と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
固形分濃度を40質量%とした以外は、実施例27と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
固形分濃度を40質量%とした以外は、実施例28と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
エネルギー線照射工程における酸素濃度を21体積%とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
加熱工程における温度を160℃とした以外は、実施例31と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
固形分濃度を40質量%とした以外は、実施例31と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
固形分濃度を40質量%とした以外は、実施例32と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
原料A1の希釈にメチルエチルケトンを用いた以外は、実施例31と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
加熱工程における温度を160℃とした以外は、実施例35と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
固形分濃度を40質量%とした以外は、実施例35と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
加熱工程における温度を160℃とした以外は、実施例37と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
<原料A3の調合>
トルエン100質量部、2-イソシアネートエチル-2,6-ジイソシアネートカプロエート50質量部、ポリカプロラクトン変性ヒドロキシエチルアクリレート(ダイセル化学工業社製プラクセルFA1)59質量部、ポリカプロラクトン変性ヒドロキシエチルアクリレート(ダイセル化学工業社製プラクセルFA5)20質量部及びハイドロキノンモノメチルエーテル0.02質量部を混合し、40℃にまで昇温して12時間保持した。その後、ポリカプロラクトントリオール(ダイセル化学工業(株)製、プラクセル308、分子量850)82質量部を加えて80℃で30分間保持した後、ジブチル錫ラウレート0.02質量部を加えて80℃で24時間保持し、トルエン111質量部を加えて固形分50質量%のウレタンアクリレートを得た。そして、このウレタンアクリレート100質量部に1-ヒドロキシ-シクロヘキシル-フェニル-ケトン3質量部を混合して活性エネルギー線硬化性組成物を調製した。
原料A3に2-(パーフルオロヘキシル)エチルアクリレートを10質量部、1-ヒドロキシ-シクロヘキシル-フェニル-ケトンを0.5質量部添加し、メチルエチルケトンとシクロヘキサノンを93:7の質量比率で混合した溶媒を用いて固形分濃度が30質量%となるように再度調整し、厚み100μmのポリエステル基材フィルム(東レ(株)製、“ルミラー”U46)上に、エージング工程後のA層厚みが30μmとなるようにワイヤーバーを用いて塗布した。塗布後、100℃で2分間、熱風乾燥機で加熱した(加熱工程)。その後、160W/cmの高圧水銀灯ランプ(アイグラフィックス(株)製)を用いて、照度600W/cm2、積算光量800mJ/cm2の紫外線を、酸素濃度0.1体積%の下で照射し(エネルギー線照射工程)、積層フィルムを得た。次に、この得られたフィルムの成型を行った。このとき延伸は行わずに予熱だけを行った。得られた結果を表1に示す。
<原料A4の調合>
トルエン100質量部、メチル-2,6-ジイソシアネートヘキサノエート25質量部、2-ヒドロキシエチルアクリレート11質量部、ポリカプロラクトン変性ヒドロキシエチルアクリレート(ダイセル化学工業社製プラクセルFA5)34質量部及びハイドロキノンモノメチルエーテル0.02質量部を混合し、40℃にまで昇温して12時間保持した。それから、ポリカプロラクトンジオール(ダイセル化学工業社製プラクセル220)141質量部を加えて80℃で30分間保持した後、ジブチル錫ラウレート0.02質量部を加えて80℃で24時間保持し、最後にトルエン111質量部を加えて固形分50質量%のウレタンアクリレートを得た。そして、このウレタンアクリレート74質量部に、トリエチレングリコールジアクリレート(共栄社化学社製ライトアクリレート3EG-A)10質量部、ステアリルアクリレート(日本油脂社製ブレンマーSA)3質量部、トルエン13質量部及び光開始剤(チバガイギー社製イルガキュア184)3質量部を混合して活性エネルギー線硬化性組成物を調製した。
原料A4を用いた以外は、実施例39と同様にして積層フィルムと成型フィルムを得た。得られた結果を表1に示す。優れた自己治癒性を示した。
原料A1を、厚み100μmのポリエステル基材フィルム(東レ(株)製、“ルミラー”U46)上に、エージング工程後のA層厚みが30μmとなるようにワイヤーバーを用いて塗布した。塗布後、160℃で2分間、熱風乾燥機で加熱した(加熱工程)。その後、40℃で14日間加熱(エージング)を行い(エージング工程)、積層フィルムを得た。次に、この得られたフィルムの成型を行った。このとき延伸は行わずに予熱だけを行った。
A層の厚みと成型延伸の倍率を変更した以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。比較例2は、成型時の延伸を縦方向に1.2倍、横方向に1.2倍の倍率で行い、エージング工程後のA層厚みが23μmとなるようにした。比較例3は、成型時の延伸を縦方向に1.3倍、横方向に1.3倍の倍率で行い、エージング工程後のA層厚みが19μmとなるようにした。得られた結果を表2に示す。A層厚みを薄くしても優れた自己治癒性を示し、また、成型不良も見られなかったが、耐汚染性は不足していた。
2-(パーフルオロヘキシル)エチルアクリレートの添加量を0.1質量部とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表2に示す。優れた自己治癒性を示したが、耐汚染性は不足していた。
2-(パーフルオロヘキシル)エチルアクリレートの添加量を30質量部とした以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表2に示す。自己治癒性は不足していたが、優れた耐汚染性を示した。
2-(パーフルオロヘキシル)エタノールの添加量を0.1質量部とした以外は、実施例10と同様にして積層フィルムと成型フィルムを得た。得られた結果を表2に示す。優れた自己治癒性を示したが、耐汚染性は不足していた。
2-(パーフルオロヘキシル)エタノールの添加量を30質量部とした以外は、実施例10と同様にして積層フィルムと成型フィルムを得た。得られた結果を表2に示す。自己治癒性は不足していたが、優れた耐汚染性を示した。
2-(パーフルオロヘキシル)エチルアクリレート100質量部に対し、1-ヒドロキシ-シクロヘキシル-フェニル-ケトンを5質量部含む組成物をメチルエチルケトンを用いて希釈し、固形分濃度40質量%の塗液を作成し、これを比較例1で得られた積層フィルムに上に、エネルギー線照射工程後の厚みが1μmとなるようにワイヤーバーを用いて塗布した。塗布後、80℃で2分間、熱風乾燥機で加熱した(加熱工程)。その後、160W/cmの高圧水銀灯ランプ(アイグラフィックス(株)製)を用いて、照度600W/cm2、積算光量800mJ/cm2の紫外線を、酸素濃度0.1体積%の下で照射した(エネルギー線照射工程)。次に、この得られたフィルムの成型を行った。このとき延伸は行わずに予熱だけを行った。
2-(パーフルオロヘキシル)エチルアクリレート10質量部の代わりにヘキサフルオロプロペントリマーを10質量部を添加した以外は、実施例1と同様にして積層フィルムと成型フィルムを得た。得られた結果を表2に示す。優れた自己治癒性を示したが、耐汚染性は不足していた。
Claims (13)
- 基材フィルムの少なくとも片側に、A層を有する積層フィルムであって、
該A層が、(1)(ポリ)カプロラクトンセグメント、および(2)ウレタン結合、を有し、
蒸留水の該A層上での接触角が95°以上120°未満、ジヨードメタンの該A層上での接触角が70°以上87°未満であることを特徴とする、積層フィルム。 - ジヨードメタンのA層上での接触角が80°以上87°未満であることを特徴とする、請求項1に記載の積層フィルム。
- 該A層が、(3)ポリシロキサンセグメント及び/またはポリジメチルシロキサンセグメント、を有することを特徴とする請求項1又は2に記載の積層フィルム。
- 積層フィルムのA層側表面について、XPSにより検出されるフッ素原子、炭素原子、窒素原子、酸素原子、ケイ素原子の合計数を100%とした際に、フッ素原子の数が0.4%以上50%以下であることを特徴とする請求項1~3のいずれかに記載の積層フィルム。
- A層の全体厚みを100%とした際に、積層フィルムのA層側表面から基材フィルム方向に向かって厚さ1%以上100%以下の範囲における、TOF-SIMSによるフッ素原子の検出強度の最大値をa、積層フィルムのA層側表面から基材フィルム方向に向かって厚さ0%以上1%未満の範囲における、TOF-SIMSによるフッ素原子の検出強度の最大値をbとしたときに、a/bが0%以上60%以下であることを特徴とする請求項1~4のいずれかに記載の積層フィルム。
- 前記a/bが、5%以上20%以下であることを特徴とする請求項5に記載の積層フィルム。
- 前記A層のTgが-30℃以上15℃以下であることを特徴とする請求項1~6のいずれかに記載の積層フィルム。
- 基材フィルムの少なくとも片側に有する層がA層の一層のみからなることを特徴とする請求項1~7のいずれかに記載の積層フィルム。
- 80℃および150℃におけるA層の平均破壊伸度が、いずれも65%以上100%未満であることを特徴とする請求項1~8のいずれかに記載の積層フィルム。
- 前記A層が、以下のフッ素化合物Aに由来する成分(以下、フッ素化合物A由来成分という)を含むことを特徴とする、請求項1~9のいずれかに記載の積層フィルム。
フッ素化合物A:下記の一般式(1)で示される化合物を指す。
B-R1-Rf ・・・一般式(1)
(上記一般式中のBは反応性部位またはヒドロキシル基を示し、R1は炭素数1から3のアルキレン基およびそれらから導出されるエステル構造を示し、Rfはフルオロアルキル基を示し、それぞれ側鎖を構造中に持ってもよい。) - 前記A層の全成分100質量%中に、フッ素化合物A由来成分を0.5質量%以上25質量%以下含むことを特徴とする、請求項10に記載の積層フィルム。
- 請求項1~11のいずれかに記載の積層フィルムを含んでなるタッチパネル。
- 請求項1~11のいずれかに記載の積層フィルムを含んでなる成型体。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020137029022A KR101931399B1 (ko) | 2011-05-16 | 2012-05-10 | 적층 필름 및 성형체 |
CN201280022170.9A CN103517808B (zh) | 2011-05-16 | 2012-05-10 | 叠层膜和成型体 |
JP2012524955A JP5928334B2 (ja) | 2011-05-16 | 2012-05-10 | 積層フィルムおよび成型体 |
EP12785632.6A EP2711182B1 (en) | 2011-05-16 | 2012-05-10 | Laminated film and molded body |
US14/116,872 US9080053B2 (en) | 2011-05-16 | 2012-05-10 | Laminated film and molded body |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011109093 | 2011-05-16 | ||
JP2011-109093 | 2011-05-16 | ||
JP2011-270982 | 2011-12-12 | ||
JP2011270982 | 2011-12-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012157500A1 true WO2012157500A1 (ja) | 2012-11-22 |
Family
ID=47176830
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2012/061942 WO2012157500A1 (ja) | 2011-05-16 | 2012-05-10 | 積層フィルムおよび成型体 |
Country Status (7)
Country | Link |
---|---|
US (1) | US9080053B2 (ja) |
EP (1) | EP2711182B1 (ja) |
JP (1) | JP5928334B2 (ja) |
KR (1) | KR101931399B1 (ja) |
CN (1) | CN103517808B (ja) |
TW (1) | TWI589439B (ja) |
WO (1) | WO2012157500A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014109177A1 (ja) * | 2013-01-09 | 2014-07-17 | 東レ株式会社 | 積層フィルム |
JP2016190436A (ja) * | 2015-03-31 | 2016-11-10 | 大日本印刷株式会社 | 積層体及び化粧板 |
JPWO2015046049A1 (ja) * | 2013-09-24 | 2017-03-09 | 東レ株式会社 | 積層フィルム |
JP2017057306A (ja) * | 2015-09-17 | 2017-03-23 | 信越化学工業株式会社 | 含フッ素硬化性組成物及び物品 |
JP2018167574A (ja) * | 2017-03-30 | 2018-11-01 | 東レフィルム加工株式会社 | 自己修復性積層体および保護フィルム |
WO2019124492A1 (ja) * | 2017-12-20 | 2019-06-27 | Agc株式会社 | 加飾フィルム、加飾フィルムの製造方法、および加飾フィルム付き3次元成形品の製造方法 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6236783B2 (ja) * | 2011-12-21 | 2017-11-29 | 東レ株式会社 | 積層フィルム |
US20150175843A1 (en) * | 2012-10-25 | 2015-06-25 | Toray Industries, Inc. | Multilayer film and molded body |
KR102314335B1 (ko) * | 2014-01-31 | 2021-10-19 | 도레이 카부시키가이샤 | 적층 필름 |
US12023875B2 (en) * | 2017-07-14 | 2024-07-02 | The University Of Rochester | Reaction injection molding of stimuli-responsive thermosets |
EP3871876A4 (en) * | 2018-10-23 | 2022-08-03 | Sumitomo Chemical Company Limited | LAMINATED BODY, FLEXIBLE ELECTRONIC DEVICE AND METHOD OF MAKING LAMINATED BODY |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07117202A (ja) * | 1993-10-21 | 1995-05-09 | Asahi Glass Co Ltd | 透明積層体及びその製造方法 |
JP2004035599A (ja) | 2002-06-28 | 2004-02-05 | Natoko Kk | ウレタン(メタ)アクリレート及びそれを含有する活性エネルギー線硬化性組成物並びにそれらの用途 |
JP2006137780A (ja) | 2004-11-10 | 2006-06-01 | Dainippon Printing Co Ltd | 成形シート |
JP2007056268A (ja) * | 1994-10-04 | 2007-03-08 | 3M Co | 反応性二液型ポリウレタン組成物及びそれから形成される任意に自己回復可能な耐引掻性のコーティング |
WO2007069765A1 (ja) * | 2005-12-16 | 2007-06-21 | Japan Advanced Institute Of Science And Technology | 自己修復材料 |
JP2009084395A (ja) | 2007-09-28 | 2009-04-23 | Mitsubishi Chemicals Corp | 重合体、組成物、硬化物および光記録媒体 |
WO2011136042A1 (ja) | 2010-04-27 | 2011-11-03 | 東レ株式会社 | 積層フィルムおよび成型体 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0710960B1 (pt) * | 2006-04-25 | 2017-10-31 | Mitsubishi Rayon Co., Ltd. | Curved coating composition by active energy ray and molded article presenting composition cured coating film |
JP4922148B2 (ja) * | 2007-02-15 | 2012-04-25 | 富士フイルム株式会社 | バリア性積層体、バリア性フィルム基板、それらの製造方法、およびデバイス |
EP1958981B1 (en) * | 2007-02-15 | 2018-04-25 | FUJIFILM Corporation | Barrier laminate, barrier film substrate, methods for producing them, and device |
US8299200B2 (en) * | 2007-06-11 | 2012-10-30 | Ndsu Research Foundation | Anchored polysiloxane-modified polyurethane coatings and uses thereof |
-
2012
- 2012-05-10 JP JP2012524955A patent/JP5928334B2/ja active Active
- 2012-05-10 US US14/116,872 patent/US9080053B2/en active Active
- 2012-05-10 CN CN201280022170.9A patent/CN103517808B/zh active Active
- 2012-05-10 KR KR1020137029022A patent/KR101931399B1/ko active IP Right Grant
- 2012-05-10 WO PCT/JP2012/061942 patent/WO2012157500A1/ja active Application Filing
- 2012-05-10 EP EP12785632.6A patent/EP2711182B1/en active Active
- 2012-05-15 TW TW101117220A patent/TWI589439B/zh active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07117202A (ja) * | 1993-10-21 | 1995-05-09 | Asahi Glass Co Ltd | 透明積層体及びその製造方法 |
JP2007056268A (ja) * | 1994-10-04 | 2007-03-08 | 3M Co | 反応性二液型ポリウレタン組成物及びそれから形成される任意に自己回復可能な耐引掻性のコーティング |
JP2004035599A (ja) | 2002-06-28 | 2004-02-05 | Natoko Kk | ウレタン(メタ)アクリレート及びそれを含有する活性エネルギー線硬化性組成物並びにそれらの用途 |
JP2006137780A (ja) | 2004-11-10 | 2006-06-01 | Dainippon Printing Co Ltd | 成形シート |
WO2007069765A1 (ja) * | 2005-12-16 | 2007-06-21 | Japan Advanced Institute Of Science And Technology | 自己修復材料 |
JP2009084395A (ja) | 2007-09-28 | 2009-04-23 | Mitsubishi Chemicals Corp | 重合体、組成物、硬化物および光記録媒体 |
WO2011136042A1 (ja) | 2010-04-27 | 2011-11-03 | 東レ株式会社 | 積層フィルムおよび成型体 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2711182A4 |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014109177A1 (ja) * | 2013-01-09 | 2014-07-17 | 東レ株式会社 | 積層フィルム |
CN104903102A (zh) * | 2013-01-09 | 2015-09-09 | 东丽株式会社 | 叠层膜 |
KR20150113950A (ko) * | 2013-01-09 | 2015-10-08 | 도레이 카부시키가이샤 | 적층 필름 |
JPWO2014109177A1 (ja) * | 2013-01-09 | 2017-01-19 | 東レ株式会社 | 積層フィルム |
TWI609784B (zh) * | 2013-01-09 | 2018-01-01 | 東麗股份有限公司 | 積層薄膜 |
KR102281542B1 (ko) * | 2013-01-09 | 2021-07-26 | 도레이 카부시키가이샤 | 적층 필름 |
JPWO2015046049A1 (ja) * | 2013-09-24 | 2017-03-09 | 東レ株式会社 | 積層フィルム |
EP3050701A4 (en) * | 2013-09-24 | 2017-06-07 | Toray Industries, Inc. | Laminated film |
JP2016190436A (ja) * | 2015-03-31 | 2016-11-10 | 大日本印刷株式会社 | 積層体及び化粧板 |
JP2017057306A (ja) * | 2015-09-17 | 2017-03-23 | 信越化学工業株式会社 | 含フッ素硬化性組成物及び物品 |
JP2018167574A (ja) * | 2017-03-30 | 2018-11-01 | 東レフィルム加工株式会社 | 自己修復性積層体および保護フィルム |
WO2019124492A1 (ja) * | 2017-12-20 | 2019-06-27 | Agc株式会社 | 加飾フィルム、加飾フィルムの製造方法、および加飾フィルム付き3次元成形品の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
EP2711182B1 (en) | 2021-06-23 |
JP5928334B2 (ja) | 2016-06-01 |
TW201300237A (zh) | 2013-01-01 |
KR101931399B1 (ko) | 2018-12-20 |
US20140171598A1 (en) | 2014-06-19 |
KR20140027207A (ko) | 2014-03-06 |
CN103517808B (zh) | 2015-11-25 |
TWI589439B (zh) | 2017-07-01 |
CN103517808A (zh) | 2014-01-15 |
EP2711182A4 (en) | 2014-10-01 |
JPWO2012157500A1 (ja) | 2014-07-31 |
US9080053B2 (en) | 2015-07-14 |
EP2711182A1 (en) | 2014-03-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5928334B2 (ja) | 積層フィルムおよび成型体 | |
JP5799806B2 (ja) | 積層フィルムおよび成型体 | |
JP5626447B2 (ja) | 積層ポリエステルフィルム、成形用部材、および成形体ならびにそれらの製造方法 | |
JP6394395B2 (ja) | 積層フィルム | |
JP7468573B2 (ja) | 積層体 | |
JP2024096196A (ja) | 硬化膜 | |
JP7006710B2 (ja) | セラミックグリーンシート製造用離型フィルム | |
JP2012139951A (ja) | 積層フィルムおよび成型体 | |
JP7200562B2 (ja) | 積層体 | |
JP4161251B2 (ja) | 白色被覆ポリエステルフィルム | |
JP7306516B2 (ja) | セラミックグリーンシート製造用離型フィルム | |
JP7035441B2 (ja) | セラミックグリーンシート製造用離型フィルム | |
JP6188118B2 (ja) | ハードコートフィルム | |
WO2015041175A1 (ja) | 積層フィルム | |
US20150175843A1 (en) | Multilayer film and molded body | |
JP7327554B2 (ja) | セラミックグリーンシート製造用離型フィルム | |
JP7306514B2 (ja) | セラミックグリーンシート製造用離型フィルム | |
JP2022016467A (ja) | セラミックグリーンシート製造用離型フィルム | |
JP2022016465A (ja) | セラミックグリーンシート製造用離型フィルム | |
JP2012166356A (ja) | 積層フィルム |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENP | Entry into the national phase |
Ref document number: 2012524955 Country of ref document: JP Kind code of ref document: A |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12785632 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012785632 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 20137029022 Country of ref document: KR Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14116872 Country of ref document: US |