JP7055166B2 - Resin film, laminate, optical member, display member and front plate - Google Patents

Description

The present invention relates to a resin film, a laminate, an optical member, a display member, and a front plate.

Conventionally, glass has been used as a base material for a display member constituting various display devices such as a solar cell or a display, a base material for an optical member, and a front plate. However, glass has the drawback of being fragile and heavy. Further, in recent years, the glass base material or the glass front plate does not have sufficient material characteristics in order to make the display thinner, lighter and more flexible. Therefore, as a material or a base material to replace glass, an acrylic resin and a laminate having scratch resistance are being studied. Composite materials of organic and inorganic materials, such as hybrid films containing polyimide and silica, have also been studied (see, for example, Patent Documents 1 and 2).

Japanese Unexamined Patent Publication No. 2008-163309 U.S. Pat. No. 8,207,256

According to the findings of the present inventors, a resin film containing a polyimide-based polymer can achieve excellent flexibility while having high transparency. However, the resin film containing the polyimide-based polymer may cause changes in contrast and hue at the time of bending, and further improvement is required in this respect. A resin film applied to a base material for a display member of a flexible device, a base material for an optical member, and / or a front plate is required to have good visibility at the time of bending.

Therefore, a main object of the present invention is to improve the visibility of a resin film containing a polyimide-based polymer and having high transparency at the time of bending.

The resin film according to one aspect of the present invention contains a polyimide-based polymer. When a light irradiation test was conducted in which the resin film was irradiated with light of 313 nm from one main surface side of the resin film for 24 hours by a light source having an output of 40 W provided at a distance of 5 cm from the resin film, the resin was subjected to the light irradiation test. The film meets the following conditions.
(I) The resin film after the light irradiation test has a transmittance of 85% or more with respect to light of 550 nm, and
(Ii) The resin film before the light irradiation test has a yellowness of 5 or less, and the difference in yellowness before and after the light irradiation test of the resin film is less than 2.5.

The resin film satisfying these conditions (i) and (ii) is unlikely to cause a change in contrast or hue at the time of bending, and can maintain good visibility.

The present invention provides a laminate having the resin film and a functional layer provided on at least one surface side of the resin film. The functional layer may be a layer having at least one function selected from the group consisting of functions of absorbing ultraviolet rays, adhesiveness, and developing high hardness on the surface.

The laminate may further have a primer layer provided between the resin film and the functional layer.

The base material of the optical member or the display member and the front plate according to one aspect of the present invention have the above resin film or laminate. These can contribute to excellent visibility during bending when applied to flexible devices.

According to the present invention, it is possible to improve the visibility of a transparent resin film containing a polyimide-based polymer at the time of bending.

It is sectional drawing which shows one Embodiment of a resin film. It is sectional drawing which shows one Embodiment of a laminated body. It is sectional drawing which shows one Embodiment of a laminated body. It is a schematic sectional drawing which shows one Embodiment of a display device.

Hereinafter, preferred embodiments of the present invention will be described in detail. However, the present invention is not limited to the following embodiments. In each figure, the same or corresponding elements are designated by the same reference numerals, and duplicate description may be omitted.

[Resin film]
FIG. 1 is a cross-sectional view showing an embodiment of a resin film. The resin film 10 shown in FIG. 1 contains a polyimide-based polymer and has a pair of main surfaces 10a and 10b facing each other.

When a light irradiation test was conducted in which the resin film 10 was irradiated with light of 313 nm from the main surface 10a side for 24 hours by a light source having an output of 40 W provided at a distance of 5 cm from the resin film 10, the resin film 10 had the following conditions. :
(I) The resin film after the light irradiation test has a transmittance of 85% or more with respect to light of 550 nm, and
(Ii) The resin film before the light irradiation test has a yellowness (YI value) of 5 or less, and the difference in yellowness before and after the light irradiation test of the resin film is less than 2.5.
Meet. The resin film satisfying these conditions (i) and (ii) is unlikely to cause a change in contrast or hue at the time of bending, and can maintain good visibility.

The resin film satisfying the conditions (i) and (ii) can be easily obtained, for example, by using a polyimide-based polymer having high transparency and incorporating an ultraviolet absorber in the resin film. Specific examples of the polyimide polymer having high transparency and the ultraviolet absorber will be described later.

The transmittance of the resin film 10 after the light irradiation test with respect to light at 550 nm is preferably 90% or more, and is usually 100% or less, and may be 95% or less. The haze of the resin film 10 after the light irradiation test is preferably 0.9 or less, and may be 0.1 or more. The resin film 10 before the light irradiation test may have a transmittance of 85% or more with respect to light of 550 nm. The transmittance of a resin film with respect to light of a predetermined wavelength means the ratio of the intensity of light of the same wavelength transmitted through the resin film to the intensity of light of a predetermined wavelength incident on the resin film. Haze can be measured according to JIS K 7105: 1981. Details of the transmittance and the method of measuring haze will be described in Examples described later.

The yellowness of the resin film 10 before the light irradiation test is preferably 4 or less, more preferably 3 or less, and may be 0.5 or more. When the yellowness before the light irradiation test is YI ₀ and the yellowness after the light irradiation is YI ₁ , the difference ΔYI in the yellowness before and after the light irradiation test of the resin film is the formula “ΔYI = YI ₁ −YI ₀ ”. _Is calculated by. ΔYI is preferably 2.3 or less, more preferably 2.0 or less, and may be 0.1 or more. Details of the method for measuring yellowness will be described in Examples described later.

The resin film 10 contains a polyimide-based polymer. In the present specification, the polyimide-based polymer means a polymer having at least one type of repeating structural unit represented by the formula (PI), the formula (a), the formula (a') or the formula (b). .. It is preferable that the repeating structural unit represented by the formula (PI) is the main structural unit of the polyimide-based polymer from the viewpoint of the strength and transparency of the film. The repeating structural unit represented by the formula (PI) is preferably 40 mol% or more, more preferably 50 mol% or more, still more preferably 70 mol%, based on all the repeating structural units of the polyimide-based polymer. The above is more preferably 90 mol% or more, and even more preferably 98 mol%.

G in the formula (PI) represents a tetravalent organic group, and A represents a divalent organic group. G ² in the formula (a) represents a trivalent organic group, and A ² represents a divalent organic group. In the formula (a'), G ³ represents a tetravalent organic group, and A ³ represents a divalent organic group. ^G4 and A4 in the formula (b) represent divalent organic groups, ^respectively .

In the formula (PI), the organic group of the tetravalent organic group represented by G (hereinafter, may be referred to as the organic group of G) includes an acyclic aliphatic group, a cyclic aliphatic group and an aromatic group. Examples are groups selected from the group consisting of. The organic group of G is preferably a tetravalent cyclic aliphatic group or a tetravalent aromatic group from the viewpoint of transparency and flexibility of the resin film 10. The aromatic group includes a monocyclic aromatic group, a fused polycyclic aromatic group, and a non-condensed polycyclic aromatic group having two or more aromatic rings linked to each other directly or by a bonding group. And so on. From the viewpoint of transparency and suppression of coloring of the resin film, the organic group of G is a cyclic aliphatic group, a cyclic aliphatic group having a fluorine-based substituent, a monocyclic aromatic group having a fluorine-based substituent, and the like. It is preferably a condensed polycyclic aromatic group having a fluorine-based substituent or a non-condensed polycyclic aromatic group having a fluorine-based substituent. As used herein, the fluorine-based substituent means a group containing a fluorine atom. The fluorine-based substituent is preferably a fluoro group (fluorine atom, —F) and a perfluoroalkyl group, and more preferably a fluoro group and a trifluoromethyl group.

More specifically, the organic group of G is, for example, a saturated or unsaturated cycloalkyl group, a saturated or unsaturated heterocycloalkyl group, an aryl group, a heteroaryl group, an arylalkyl group, an alkylaryl group, a heteroalkylaryl. It is selected from groups that have a group and any two of these (which may be the same) and are linked to each other directly or by a linking group. Examples of the bonding group include -O-, an alkylene group having 1 to 10 carbon atoms, -SO _2- , -CO- or -CO-NR- (R is a methyl group, an ethyl group, a propyl group, etc., having 1 to 1 carbon atoms. 3 represents an alkyl group or a hydrogen atom).

The tetravalent organic group represented by G usually has 2 to 32 carbon atoms, preferably 4 to 15 carbon atoms, more preferably 5 to 10 carbon atoms, and further preferably 6 to 8 carbon atoms. When the organic group of G is a cyclic aliphatic group or an aromatic group, at least one of the carbon atoms constituting these groups may be replaced with a heteroatom. Examples of the heteroatom include O, N or S.

Specific examples of G include the groups represented by the following formulas (20), formulas (21), formulas (22), formulas (23), formulas (24), formulas (25) or formulas (26). Will be. * In the formula indicates a bond. Z in the formula (26) is a single bond, -O-, -CH _2- , -C (CH ₃ ) _2- , -Ar-O-Ar-, -Ar-CH ₂ -Ar-, -Ar- Represents C (CH ₃ ) ₂ -Ar- or -Ar-SO ₂ -Ar-. Ar is represented by an aryl group having 6 to 20 carbon atoms, and may be, for example, a phenylene group. At least one of the hydrogen atoms of these groups may be substituted with a fluorine-based substituent.

In the formula (PI), the organic group of the divalent organic group represented by A (hereinafter, may be referred to as the organic group of A) includes an acyclic aliphatic group, a cyclic aliphatic group and an aromatic group. Examples are groups selected from the group consisting of. The divalent organic group represented by A is preferably selected from a divalent cyclic aliphatic group and a divalent aromatic group. The aromatic group includes a monocyclic aromatic group, a fused polycyclic aromatic group, and a non-condensed polycyclic aromatic group having two or more aromatic rings, which are directly or linked to each other by a bonding group. The group is mentioned. From the viewpoint of transparency and suppression of coloring of the resin film, it is preferable that a fluorine-based substituent is introduced into the organic group of A.

More specifically, the organic group of A is, for example, a saturated or unsaturated cycloalkyl group, a saturated or unsaturated heterocycloalkyl group, an aryl group, a heteroaryl group, an arylalkyl group, an alkylaryl group, a heteroalkylaryl. It is selected from groups that have a group and any two of these (which may be the same) and to which they are directly linked or linked to each other by a linking group. Examples of the hetero atom include O, N or S, and examples of the bonding group include -O-, an alkylene group having 1 to 10 carbon atoms, -SO _2- , -CO- or -CO-NR- (R is methyl). Examples thereof include an alkyl group having 1 to 3 carbon atoms such as a group, an ethyl group, and a propyl group, or a hydrogen atom).

The number of carbon atoms of the divalent organic group represented by A is usually 2 to 40, preferably 5 to 32, more preferably 12 to 28, and further preferably 24 to 27.

Specific examples of A include a group represented by the following formula (30), formula (31), formula (32), formula (33) or formula (34). * In the formula indicates a bond. Z ¹ to Z ³ are independently single-bonded, -O-, -CH _2- , -C (CH ₃ ) _2- , -SO _2- , -CO- or -CO-NR- (R is Represents an alkyl group having 1 to 3 carbon atoms such as a methyl group, an ethyl group, and a propyl group, or a hydrogen atom). In the following groups, Z ¹ and Z ² and Z ² and Z ³ are preferably in the meta or para position with respect to each ring, respectively. It is preferable that the single bond between Z ¹ and the terminal, the single bond between Z ² and the terminal, and the single bond between Z ³ and the terminal are in the meta-position or the para-position, respectively. In one example of A, Z ¹ and Z ³ are -O- and Z ² is -CH _2- , -C (CH ₃ ) _2- or -SO _2- . One or more of the hydrogen atoms of these groups may be substituted with a fluorinated substituent.

At least one hydrogen atom among the hydrogen atoms constituting at least one of A and G is selected from the group consisting of a fluorine-based substituent, a hydroxyl group, a sulfone group, an alkyl group having 1 to 10 carbon atoms, and the like. It may be substituted with a functional group. When the organic group of A and the organic group of G are cyclic aliphatic groups or aromatic groups, respectively, it is preferable that at least one of A and G has a fluorine-based substituent, and both A and G are fluorine. It is more preferable to have a system substituent.

G ² in the formula (a) is a trivalent organic group. This organic group can be selected from the same groups as the organic group of G in the formula (PI) except that it is a trivalent group. As an example of G ² , a group in which any one of the four bonds of the groups represented by the formulas (20) to (26) given as a specific example of G is replaced with a hydrogen atom is mentioned. Can be done. A ² in the formula (a) can be selected from the same groups as A in the formula (PI).

G ³ in the formula (a') can be selected from the same groups as the organic group of G in the formula (PI). A3 in formula (a') can be selected from the same groups as A in formula ⁽ PI).

G4 in the formula (b) is a ^divalent organic group. This organic group can be selected from the same groups as the organic group of G in the formula (PI) except that it is a divalent group. As an example of G ⁴ , a group in which any two of the four bonds of the groups represented by the formulas (20) to (26) given as specific examples of G are replaced with hydrogen atoms is mentioned. Can be done. A4 in formula (b) can be selected from the same groups as A in formula ⁽ PI).

The polyimide-based polymer contained in the resin film 10 includes diamines and a tetracarboxylic acid compound (including an acid chloride compound and a tetracarboxylic acid compound analog such as a tetracarboxylic acid dianhydride) or a tricarboxylic acid compound (acid chloride compound). And a condensate type polymer obtained by polycondensing with at least one of (including tricarboxylic acid compound analogs such as tricarboxylic acid anhydride). Further, a dicarboxylic acid compound (including an analog such as an acid chloride compound) may be polycondensed. The repeating structural unit represented by the formula (PI) or the formula (a') is usually derived from diamines and tetracarboxylic acid compounds. The repeating structural unit represented by the formula (a) is usually derived from diamines and tricarboxylic acid compounds. The repeating structural unit represented by the formula (b) is usually derived from diamines and dicarboxylic acid compounds.

Examples of the tetracarboxylic acid compound include aromatic tetracarboxylic acid compounds, alicyclic tetracarboxylic acid compounds and acyclic aliphatic tetracarboxylic acid compounds. These may be used in combination of two or more. The tetracarboxylic acid compound is preferably a tetracarboxylic acid dianhydride, and examples of the tetracarboxylic acid dianhydride include aromatic tetracarboxylic acid dianhydride, alicyclic tetracarboxylic acid dianhydride, and acyclic fat. Examples thereof include group tetracarboxylic acid dianhydride.

The tetracarboxylic acid compound is selected from an alicyclic tetracarboxylic acid compound and an aromatic tetracarboxylic acid compound from the viewpoint of solubility of the polyimide-based polymer in a solvent and transparency and flexibility when the resin film 10 is formed. Is preferable. From the viewpoint of transparency and suppression of coloring of the resin film, the tetracarboxylic acid compound may be selected from an alicyclic tetracarboxylic acid compound having a fluorine-based substituent and an aromatic tetracarboxylic acid compound having a fluorine-based substituent. It is more preferable that it is an alicyclic tetracarboxylic acid compound having a fluorine-based substituent.

Examples of the tricarboxylic acid compound include aromatic tricarboxylic acids, alicyclic tricarboxylic acids, acyclic aliphatic tricarboxylic acids and their related acid chloride compounds, acid anhydrides and the like. The tricarboxylic acid compound is preferably selected from aromatic tricarboxylic acids, alicyclic tricarboxylic acids, acyclic aliphatic tricarboxylic acids and related acid chloride compounds thereof. Two or more kinds of tricarboxylic acid compounds may be used in combination.

The tricarboxylic acid compound may be selected from an alicyclic tricarboxylic acid compound and an aromatic tricarboxylic acid compound from the viewpoint of solubility of the polyimide-based polymer in a solvent and transparency and flexibility when the resin film 10 is formed. preferable. From the viewpoint of transparency and suppression of coloring of the resin film, the tricarboxylic acid compound is preferably selected from an alicyclic tricarboxylic acid compound having a fluorine-based substituent and an aromatic tricarboxylic acid compound having a fluorine-based substituent.

Examples of the dicarboxylic acid compound include aromatic dicarboxylic acid, alicyclic dicarboxylic acid, acyclic aliphatic dicarboxylic acid and acid chloride compounds related thereto, acid anhydride and the like. The dicarboxylic acid compound is preferably selected from aromatic dicarboxylic acids, alicyclic dicarboxylic acids, acyclic aliphatic dicarboxylic acids and related acid chloride compounds thereof. Two or more kinds of dicarboxylic acid compounds may be used in combination.

The dicarboxylic acid compound may be selected from an alicyclic dicarboxylic acid compound and an aromatic dicarboxylic acid compound from the viewpoint of solubility of the polyimide-based polymer in a solvent and transparency and flexibility when the resin film 10 is formed. preferable. From the viewpoint of transparency of the resin film and suppression of coloring, the dicarboxylic acid compound is preferably selected from an alicyclic dicarboxylic acid compound having a fluorine-based substituent and an aromatic dicarboxylic acid compound having a fluorine-based substituent.

Examples of diamines include aromatic diamines, alicyclic diamines and aliphatic diamines. These may be used in combination of two or more. The diamines are selected from alicyclic diamines and aromatic diamines having a fluorine-based substituent from the viewpoints of solubility of the polyimide polymer in a solvent and transparency and flexibility when the resin film 10 is formed. Is preferable.

When such a polyimide polymer is used, it has particularly excellent flexibility, high light transmittance (for example, 85% or more, preferably 88% or more with respect to light of 550 nm), and low yellowness (YI). It is easy to obtain a resin film having a value, for example, 5 or less, preferably 3 or less), and a low haze (for example, 1.5% or less, preferably 1.0% or less).

The polyimide-based polymer may be a copolymer containing a plurality of different types of the above-mentioned repeating structural units. The weight average molecular weight of the polyimide polymer is usually 10,000 to 500,000. The weight average molecular weight of the polyimide polymer is preferably 50,000 to 500,000, more preferably 70,000 to 400,000. The weight average molecular weight is a standard polystyrene-equivalent molecular weight measured by gel permeation chromatography (GPC). If the weight average molecular weight of the polyimide polymer is large, high flexibility tends to be obtained, but if the weight average molecular weight of the polyimide polymer is too large, the viscosity of the varnish tends to increase and the processability tends to decrease. be.

The polyimide-based polymer may contain a halogen atom such as a fluorine atom that can be introduced by the above-mentioned fluorine-based substituent or the like. Since the polyimide polymer contains a halogen atom, the elastic modulus of the resin film can be improved and the yellowness can be reduced. As a result, scratches and wrinkles generated on the resin film can be suppressed, and the transparency of the resin film can be improved. The halogen atom is preferably a fluorine atom. The content of the halogen atom in the polyimide-based polymer is preferably 1 to 40% by mass, more preferably 1 to 30% by mass, based on the mass of the polyimide-based polymer.

The resin film 10 may contain one kind or two or more kinds of ultraviolet absorbers. The ultraviolet absorber can be appropriately selected from those usually used as an ultraviolet absorber in the field of resin materials. The ultraviolet absorber may contain a compound that absorbs light having a wavelength of 400 nm or less. Examples of the ultraviolet absorber that can be appropriately combined with the polyimide-based polymer include at least one compound selected from the group consisting of benzophenone-based compounds, salicylate-based compounds, benzotriazole-based compounds, and triazine-based compounds.
As used herein, the term "system compound" refers to a derivative of a compound to which the "system compound" is attached. For example, the "benzophenone-based compound" refers to a compound having benzophenone as a maternal skeleton and a substituent bonded to benzophenone.

The blending amount of the ultraviolet absorber may be such that the resin film 10 satisfies the above-mentioned conditions (i) and (ii). Specifically, the amount of the ultraviolet absorber is usually 1% by mass or more, preferably 2% by mass or more, preferably 3% by mass or more, and usually, with respect to the total mass of the resin film. It is 10% by mass or less, preferably 8% by mass or less, and preferably 6% by mass or less.

The resin film 10 may further contain an inorganic material such as inorganic particles. The inorganic material is preferably a silicon material containing a silicon atom. When the resin film 10 contains an inorganic material such as a silicon material, a particularly excellent effect can be obtained in terms of flexibility.

Examples of the silicon material containing a silicon atom include silica particles, a quaternary alkoxysilane such as tetraethyl orthosilicate (TEOS), and a silicon compound such as a silsesquioxane derivative. Among these silicon materials, silica particles are preferable from the viewpoint of transparency and flexibility of the resin film 10.

The average primary particle size of the silica particles is usually 100 nm or less. When the average primary particle diameter of the silica particles is 100 nm or less, the transparency tends to be improved.

The average primary particle diameter of the silica particles in the resin film can be determined by observation with a transmission electron microscope (TEM). The primary particle diameter of the silica particles can be a directional diameter by a transmission electron microscope (TEM). The average primary particle diameter can be obtained by measuring the primary particle diameter at 10 points by TEM observation and as an average value thereof. The particle distribution of the silica particles before forming the resin film can be obtained by a commercially available laser diffraction type particle size distribution meter.

In the resin film 10, the blending ratio of the polyimide polymer and the inorganic material is preferably 1: 9 to 10: 0 in terms of mass ratio, with the total of both being 10, preferably 3: 7 to 10: 0. It is more preferably 3: 7 to 8: 2, and even more preferably 3: 7 to 7: 3. The ratio of the inorganic material to the total mass of the polyimide-based polymer and the inorganic material is usually 20% by mass or more, preferably 30% by mass or more, and usually 90% by mass or less, 70% by mass or less. Is preferable. When the compounding ratio of the polyimide-based polymer and the inorganic material is within the above range, the transparency and mechanical strength of the resin film tend to be improved.

The resin film 10 may further contain other components as long as the transparency and flexibility are not significantly impaired. Examples of other components include antioxidants, mold release agents, stabilizers, colorants such as brewing agents, flame retardants, lubricants and leveling agents. The ratio of the components other than the polyimide-based polymer and the inorganic material is preferably more than 0% and 20% by mass or less, more preferably more than 0% and 10% by mass or less, based on the mass of the resin film 10. Is.

When the resin film 10 contains a polyimide-based polymer and a silicon material, it is preferable that Si / N, which is the ratio of the number of atoms of silicon atoms to nitrogen atoms on at least one main surface 10a, is 8 or more. This atomic number ratio Si / N is determined by evaluating the composition of the main surface 10a by X-ray Photoelectron Spectroscopy (XPS), and from the abundance of silicon atoms and the abundance of nitrogen atoms obtained thereby. It is a calculated value.

When the Si / N on the main surface 10a of the resin film 10 is 8 or more, sufficient adhesion to the functional layer 20 described later can be obtained. From the viewpoint of adhesion, the Si / N is more preferably 9 or more, further preferably 10 or more, preferably 50 or less, and even more preferably 40 or less.

The thickness of the resin film 10 is appropriately adjusted depending on the flexible device to which the laminate 30 is applied, but is preferably 10 to 500 μm, more preferably 15 to 200 μm, and 20 to 100 μm. Is even more preferable. The resin film 10 having such a structure has particularly excellent flexibility.

Next, an example of the method for manufacturing the resin film 10 of the present embodiment will be described. The polyimide-based polymer varnish used for producing a resin film is prepared by dissolving a polyimide-based polymer soluble in a solvent polymerized by a known method for synthesizing a polyimide-based polymer in a solvent. The solvent may be any solvent that dissolves a polyimide polymer, and for example, dimethylacetamide (DMAC), dimethylformamide (DMF), dimethyl sulfoxide (DMSO), γ-butyrolactone (GBL), and a mixed solvent thereof may be used. Can be mentioned.

When producing a resin film containing an inorganic material, the inorganic material is added to a polyimide-based polymer varnish, and the mixture is stirred and mixed by a known stirring method to prepare a dispersion liquid in which the inorganic material is uniformly dispersed. When an ultraviolet absorber is blended, the ultraviolet absorber can be added to this dispersion.

The polyimide-based polymer varnish or dispersion may further contain additives. Examples of the additive include a colorant such as an antioxidant, a mold release agent, a stabilizer and a brewing agent, a flame retardant, a lubricant, a thickener and a leveling agent. The polyimide-based polymer varnish or dispersion may contain a compound such as alkoxysilane having one or two or more metal alkoxide groups, which contributes to the bonding between the inorganic particles. Examples of such compounds include alkoxysilanes having an amino group. By using a polyimide-based polymer varnish or a dispersion liquid containing such a compound, it is possible to increase the blending ratio of the inorganic particles while maintaining the optical characteristics such as the transparency of the resin film.

The polyimide-based polymer varnish or dispersion may further contain water. The content of water is usually 0.1 to 10% by mass with respect to the mass of the polyimide-based polymer varnish or the dispersion liquid.

The resin film can be produced by an appropriate known method. Examples of the manufacturing method include the following methods. The above-mentioned polyimide-based polymer varnish or dispersion is applied to a substrate by a known roll-to-roll or batch method to form a coating film. The coating film is dried to form a film. Then, the resin film 10 is obtained by peeling the film from the base material. Examples of the base material include a polyethylene terephthalate (PET) base material, a stainless steel (SUS) belt, a glass base material, and the like.

The coating may be heated for drying and / or baking of the coating. The heating temperature of the coating film is usually 50 to 350 ° C. The coating film may be heated under an inert atmosphere or under reduced pressure. The solvent can be evaporated and removed by heating the coating film. The resin film may be formed by a method including a step of drying the coating film at 50 to 150 ° C. and a step of baking the dried coating film at 180 to 350 ° C.

Next, at least one main surface of the resin film may be surface-treated. The surface treatment is preferably UV ozone treatment. By UV ozone treatment, Si / N can be easily set to 8 or more. However, the method of setting Si / N to 8 or more is not limited to UV ozone treatment. The main surface 10a and / or 10b of the resin film 10 may be subjected to surface treatment such as plasma treatment or corona discharge treatment in order to improve the adhesion to the functional layer described later.

The UV ozone treatment can be performed using a known ultraviolet light source containing a wavelength of 200 nm or less. An example of an ultraviolet light source is a low pressure mercury lamp. As the ultraviolet light source, various commercially available devices equipped with an ultraviolet light source may be used. Examples of the commercially available device include an ultraviolet (UV) ozone cleaning device UV-208 manufactured by Technovision.

The resin film 10 of the present embodiment thus obtained is excellent in flexibility. Further, when Si / N, which is the atomic number ratio of silicon atom and nitrogen atom, is 8 or more on at least one main surface 10a, excellent adhesion to the functional layer 20 described later can be obtained.

[Laminate]
FIG. 2 is a cross-sectional view showing an embodiment of the laminated body. The laminate 30 shown in FIG. 2 is a laminate having a resin film 10 and a functional layer 20 laminated on one main surface 10a of the resin film 10.

The functional layer 20 may be a layer for imparting further functions (performance) to the laminated body 30 when the laminated body 30 is used as a base material of an optical member or a display member of a flexible device or a front plate. Here, in the present specification, the optical member means a sensor unit such as a touch sensor or a signal transmitting unit in a display device, and the display member means an image display unit such as an organic EL device or a liquid crystal display device in a display device. do.

The functional layer 20 is preferably a layer having at least one function selected from the group consisting of ultraviolet absorption, a function of exhibiting high hardness on the surface, adhesiveness, hue adjustment, and refractive index adjustment.

The layer having an ultraviolet absorbing function (ultraviolet absorbing layer) as the functional layer 20 includes, for example, a main material selected from an ultraviolet curable transparent resin, an electron beam curable transparent resin, and a heat curable transparent resin. , Consists of an ultraviolet absorber dispersed in this main material. By providing the ultraviolet absorbing layer as the functional layer 20, the change in yellowness due to light irradiation can be easily suppressed.

The ultraviolet curable type, electron beam curable type, or thermosetting type transparent resin as the main material of the ultraviolet absorption layer is not particularly limited, but may be, for example, poly (meth) acrylate. The ultraviolet absorber can be selected from the same compounds as those exemplified as the ultraviolet absorber that can be contained in the resin film 10.

The ultraviolet absorbing layer may be a layer that absorbs 95% or more of light having a wavelength of 400 nm or less (for example, light having a wavelength of 313 nm). In other words, the ultraviolet absorbing layer may be a layer having a transmittance of less than 5% for light having a wavelength of 400 nm or less (for example, light having a wavelength of 313 nm). The ultraviolet absorbing layer can contain an ultraviolet absorber having a concentration at which such a transmittance can be obtained. From the viewpoint of suppressing the increase in yellowness of the laminated body due to light irradiation, the ratio of the content of the ultraviolet absorber in the ultraviolet absorbing layer (functional layer 20) is usually 1% by mass or more based on the mass of the ultraviolet absorbing layer. Yes, preferably 3% by mass or more, usually 10% by mass or less, and preferably 8% by mass or less.

The layer (hard coat layer) having a function of exhibiting high hardness on the surface as the functional layer 20 is, for example, a layer that gives the laminate a surface having a pencil hardness higher than the pencil hardness of the surface of the resin film. The hard coat layer is not particularly limited, and includes an ultraviolet curable type, an electron beam curable type, or a thermosetting type resin represented by poly (meth) acrylates. The hard coat layer may contain a photopolymerization initiator and an organic solvent. Poly (meth) acrylates are poly (meth) acrylates formed from, for example, one or more (meth) acrylates selected from polyurethane (meth) acrylates, epoxy (meth) acrylates, and other polyfunctional poly (meth) acrylates. Meta) Acrylate. In addition to the above components, the hardcoat layer may contain inorganic oxides such as silica, alumina, and polyorganosiloxane.

The layer having an adhesive function (adhesive layer) as the functional layer 20 has a function of adhering the laminated body 30 to another member. Examples of the material for forming the pressure-sensitive adhesive layer include a thermosetting resin composition and a photocurable resin composition.

The adhesive layer may be composed of a resin composition containing a component having a polymerizable functional group. In this case, strong adhesion can be realized by further polymerizing the resin composition constituting the adhesive layer after the laminated body 30 is brought into close contact with another member. The adhesive strength between the resin film 10 and the adhesive layer is preferably 0.1 N / cm or more, more preferably 0.5 N / cm or more.

The adhesive layer may contain a thermosetting resin composition or a photocurable resin composition as a material. In this case, the resin composition can be polymerized and cured by supplying energy after the fact.

The adhesive layer may be a layer called a pressure-sensitive adhesive (PSA), which is attached to an object by pressing. The pressure-sensitive adhesive may be an adhesive that is "a substance that has adhesiveness at room temperature and adheres to the adherend with a light pressure" (JIS K6800), and "protects a specific component (microcapsules). It may be a capsule type adhesive which is "an adhesive which can maintain stability until the film is broken by an appropriate means (pressure, heat, etc.)" (JIS K6800).

The layer having a hue adjusting function (hue adjusting layer) as the functional layer 20 is a layer capable of adjusting the laminated body 30 to a desired hue. The hue adjusting layer may be, for example, a layer containing a resin and a colorant. Examples of the colorant include titanium oxide, zinc oxide, petals, titanium oxide-based firing pigments, ultramarine, cobalt aluminate, and carbon black and other inorganic pigments; azo compounds, quinacridone compounds, anthracinone compounds, and perylene compounds. Organic pigments such as compounds, isoindolinone compounds, phthalocyanine compounds, quinophthalone compounds, slene compounds and diketopyrrolopyrrole compounds; extender pigments such as barium sulfate and calcium carbonate; basic dyes, acid dyes and medial dyes. Etc. can be mentioned.

The layer having the function of adjusting the refractive index (refractive index adjusting layer) as the functional layer 20 is a layer having a refractive index different from that of the resin film 10 and capable of imparting a predetermined refractive index to the laminated body. .. The refractive index adjusting layer may be, for example, a resin layer appropriately selected, and if necessary, a resin layer further containing a pigment, or may be a thin film of metal.

Examples of the pigment for adjusting the refractive index include silicon oxide, aluminum oxide, antimony oxide, tin oxide, titanium oxide, zirconium oxide and tantalum oxide. The average particle size of the pigment is preferably 0.1 μm or less. By setting the average particle size of the pigment to 0.1 μm or less, diffuse reflection of light transmitted through the refractive index adjusting layer can be prevented, and deterioration of transparency can be prevented.

Examples of the metal used for the refractive index adjusting layer include metals such as titanium oxide, tantalum oxide, zirconium oxide, zinc oxide, tin oxide, silicon oxide, indium oxide, titanium nitride, titanium nitride, silicon nitride, and silicon nitride. Examples include oxides or metal nitrides.

The functional layer 20 has the above-mentioned functions as appropriate depending on the use of the laminated body 30. The functional layer 20 may be a single layer or a plurality of layers. Each layer may have one function or two or more functions.

The functional layer 20 preferably has a function of exhibiting high hardness on the surface and a function of absorbing ultraviolet rays. In this case, the functional layer 20 is a multilayer including "a single layer having a function of developing high hardness on the surface and a function of absorbing ultraviolet rays" and "a layer having a function of expressing high hardness on the surface and a layer having ultraviolet absorption". "Or, it is preferable to include" a single layer having a function of developing high hardness on the surface and a function of absorbing ultraviolet rays and a multilayer including a layer having a function of developing high hardness on the surface ".

The thickness of the functional layer 20 is appropriately adjusted depending on the flexible device to which the laminated body 30 is applied, but is preferably 1 to 100 μm, more preferably 2 to 80 μm. The functional layer 20 is typically thinner than the resin film 10.

The laminated body 30 can be obtained by forming the functional layer 20 on the main surface 10a of the resin film 10. The functional layer 20 can be formed by a known roll-to-roll or batch method.

For the ultraviolet absorbing layer as the functional layer 20, for example, a dispersion liquid containing an ultraviolet absorber and a main material such as a resin in which the ultraviolet absorber is dispersed is applied to the main surface 10a of the resin film 10 to form a coating film. It can be formed by forming and drying and curing the coating film.

For the hard coat layer as the functional layer 20, for example, a solution containing a resin for forming a hard coat layer is applied to the main surface 10a of the resin film 10 to form a coating film, and the coating film is dried and cured. Can be formed by

The adhesive layer as the functional layer 20 is formed by, for example, applying a solution containing an adhesive for forming the adhesive layer to the main surface 10a of the resin film 10 to form a coating film, and drying and curing the coating film. , Can be formed.

As the hue adjusting layer as the functional layer 20, for example, a dispersion liquid containing a pigment or the like forming the hue adjusting layer and a main material such as a resin in which the pigment or the like is dispersed is applied to the main surface 10a of the resin film 10. It can be formed by forming a coating film and drying and curing the coating film.

The refractive index adjusting layer as the functional layer 20 is dispersed, for example, on the main surface 10a of the resin film 10 including inorganic particles or the like forming the refractive index adjusting layer and a main material such as a resin in which the inorganic particles or the like are dispersed. It can be formed by applying a liquid to form a coating film, and drying and curing the coating film.

The single layer having the function of exhibiting high hardness on the surface and the function of absorbing ultraviolet rays as the functional layer 20 is mainly composed of an ultraviolet absorber and a resin in which the ultraviolet absorber is dispersed on the main surface 10a of the resin film 10. It can be formed by applying a dispersion liquid containing a material and a resin forming a hard coat layer to form a coating film, and drying and curing the coating film. The resin used as the main material and the resin forming the hard coat layer may be the same.

A multi-layered functional layer including a layer having a function of exhibiting high hardness on the surface and a layer having a function of absorbing ultraviolet rays can be formed by the following method.
A dispersion liquid containing an ultraviolet absorber and a main material such as a resin in which the ultraviolet absorber is dispersed is applied to the main surface 10a of the resin film 10 to form a coating film, and the coating film is dried and cured. To form an ultraviolet absorbing layer. Next, a solution containing a resin that forms a hardcoat layer may be applied to the ultraviolet absorbing layer to form a coating film, and the coating film may be dried and cured to form a hardcoat layer. By this method, a multi-layered functional layer including a layer having a function of exhibiting high hardness on the surface and a layer having a function of absorbing ultraviolet rays is formed.

A multilayer including a single layer having a function of developing high hardness on the surface and a function of absorbing ultraviolet rays and a layer having a function of developing high hardness on the surface can be formed by the following method.
A dispersion liquid containing an ultraviolet absorber, a main material such as a resin in which the ultraviolet absorber is dispersed, and a resin forming a hard coat layer is applied to the main surface 10a of the resin film 10 to form a coating film. The coating film is dried and cured to form a single layer having a function of developing high hardness and a function of absorbing ultraviolet rays on the surface, and a solution containing a resin for forming a hard coat layer is further formed on the single layer. A hard coat layer may be formed by applying to form a coating film and drying and curing the coating film. By this method, a multi-layered functional layer including a layer having a function of developing high hardness on the surface and a function of absorbing ultraviolet rays and a layer having a function of developing high hardness on the surface is formed.

The laminated body 30 of the present embodiment thus obtained is excellent in flexibility. The laminated body 30 has functionality such as transparency, ultraviolet resistance characteristics, and a function of exhibiting high hardness on the surface, which are required when applied to the base material of the optical member or the display member of the flexible device or the front plate. be able to. When the Si / N on the main surface 10a of the resin film 10 is 8 or more, the laminated body 30 is also excellent in adhesion between the resin film 10 and the functional layer 20.

FIG. 3 is also a cross-sectional view showing an embodiment of the laminated body. The laminate 30 shown in FIG. 3 has the same resin film 10 and functional layer 20 as the laminate of FIG. 2, and further has a primer layer 25 provided between the resin film 10 and the functional layer 20. There is. The primer layer 25 is laminated on one main surface 10a of the resin film 10. The functional layer 20 is laminated on the main surface 25a on the side opposite to the main surface in contact with the resin film 10 of the primer layer 25.

The primer layer 25 is a layer formed of a primer agent, and preferably contains a material capable of enhancing the adhesion to the resin film 10 and the functional layer 20. The compound contained in the primer layer 25 may be chemically bonded to the polyimide-based polymer or silicon material contained in the resin film 10 at the interface.

Examples of the primer agent include a primer agent for an ultraviolet curable type, a thermosetting type, or a two-component curable type epoxy compound. The primer agent may be a polyamic acid. These primer agents are suitable for enhancing the adhesion to the resin film 10 and the functional layer 20.

The primer agent may contain a silane coupling agent. The silane coupling agent may be chemically bonded to the silicon material contained in the resin film 10 by a condensation reaction. The silane coupling agent can be suitably used particularly when the compounding ratio of the silicon material contained in the resin film 10 is high.

Examples of the silane coupling agent include compounds having an alkoxysilyl group having a silicon atom and 1 to 3 alkoxy groups covalently bonded to the silicon atom. A compound containing a structure in which two or more alkoxy groups are covalently bonded to a silicon atom is preferable, and a compound containing a structure in which three alkoxy groups are covalently bonded to a silicon atom is more preferable. Examples of the alkoxy group include a methoxy group, an ethoxy group, an isopropoxy group, an n-butoxy group, a t-butoxy group and the like. Of these, the methoxy group and the ethoxy group are preferable because they can enhance the reactivity with the silicon material.

The silane coupling agent preferably has a substituent having a high affinity with the resin film 10 and the functional layer 20. From the viewpoint of compatibility with the polyimide-based polymer contained in the resin film 10, the substituent of the silane coupling agent is preferably an epoxy group, an amino group, a ureido group or an isocyanate group. When the functional layer 20 contains (meth) acrylates, if the silane coupling agent used for the primer layer 25 has an epoxy group, a methacrylic group, an acrylic group, an amino group or a styryl group, the affinity is enhanced. preferable. Among these, a silane coupling agent having a substituent selected from a methacrylic group, an acrylic group, and an amino group is preferable because it tends to have an excellent affinity with the resin film 10 and the functional layer 20.

The thickness of the primer layer 25 is appropriately adjusted according to the functional layer 20, but is preferably 0.01 nm to 20 μm. When a primer agent of an epoxy compound is used, the thickness of the primer layer 25 is preferably 0.01 μm to 20 μm, more preferably 0.1 μm to 10 μm. When a silane coupling agent is used, the thickness of the primer layer 25 is preferably 0.1 nm to 1 μm, more preferably 0.5 nm to 0.1 μm.

In the laminate 30 of FIG. 3, for example, a solution in which a primer is dissolved is applied to the main surface 10a of the resin film 10 to form a coating film, and the formed coating film is dried and cured to form a primer layer. It can be manufactured by a method including the above. The method of forming the other members is the same as that of the laminated body 30 of FIG. The primer layer 25 may be cured at the same time as the functional layer 20, or may be separately cured before forming the functional layer 20.

The resin film and the laminate of the present embodiment have high transparency and can maintain excellent visibility at the time of bending. In addition, the resin film and the laminate can also have excellent flexibility. When a primer layer is provided between the resin film and the functional layer, the adhesion between the resin film and the functional layer is high. The resin film and the laminate have functionality such as transparency, ultraviolet resistance, and a function of exhibiting high hardness on the surface, which are required when applied to the base material of the optical member or the display member of the flexible device or the front plate. Can have.

The configurations of the resin film and the laminate can be appropriately deformed. For example, functional layers can be provided on both sides of the resin film. In this case, a primer layer may be provided between each functional layer and the resin film.

[Display device (flexible device)]
FIG. 4 is a cross-sectional view showing an embodiment of a display device. The display device 100 shown in FIG. 4 has an organic EL device 50, a touch sensor 70, and a front plate 90. These are usually housed in a housing. The organic EL device 50 and the touch sensor 70, and the touch sensor 70 and the front plate 90 are bonded with, for example, an optical adhesive (Optical Clear Adhesive) (not shown).

The organic EL device 50 is a display member having an organic EL element 51, a first substrate 55, a second substrate 56, and a sealing material 59.

The organic EL element 51 has a pair of electrodes (first electrode 52 and second electrode 53) and a light emitting layer 54. The light emitting layer 54 is arranged between the first electrode 52 and the second electrode 53.

The first electrode 52 is formed of a light-transmitting conductive material. The second electrode 53 may also have light transmission. Known materials can be used as the first electrode 52 and the second electrode 53.

The light emitting layer 54 can be formed of a known light emitting material constituting the organic EL element. The light emitting material may be either a low molecular weight compound or a high molecular weight compound.

When electric power is supplied between the first electrode 52 and the second electrode 53, carriers (electrons and holes) are supplied to the light emitting layer 54, and light is generated in the light emitting layer 54. The light generated in the light emitting layer 54 is emitted to the outside of the organic EL device 50 via the first electrode 52 and the first substrate 55.

The first substrate 55 is formed of a light-transmitting material. The second substrate 56 may have light transmission. The first substrate 55 and the second substrate 56 are bonded to each other by a sealing material 59 arranged so as to surround the periphery of the organic EL element. The first substrate 55, the second substrate 56, and the sealing material 59 form a sealing structure for internally sealing the organic EL element. The first substrate 55 and / or the second substrate 56 is often a gas barrier material.

As a material for forming either or both of the first substrate 55 and the second substrate 56, an inorganic material such as glass or a known transparent resin such as an acrylic resin can be used. As these members, the resin film or laminate according to the present embodiment described above can also be adopted.

The first substrate 55 and the second substrate 56 that can adopt the laminate according to the present embodiment correspond to the base material or the gas barrier material of the display member in the present embodiment. Since the organic EL device 50 having such a first substrate 55 and a second substrate 56 adopts the resin film or laminate according to the present embodiment, it is excellent in flexibility.

The touch sensor 70 is an optical member having a touch sensor base material 71 and an element layer 72 having a detection element formed on the touch sensor base material 71.

The touch sensor base material 71 is formed of a light-transmitting material. As the touch sensor base material 71, an inorganic material such as glass or a known transparent resin such as an acrylic resin can be used. As the touch sensor base material 71, the resin film or laminate according to the present embodiment described above can also be adopted.

A known detection element composed of a semiconductor element, wiring, resistance, or the like is formed on the element layer 72. As the configuration of the detection element, a configuration that realizes a known detection method such as a matrix switch, a resistance film method, and a capacitance type can be adopted.

The touch sensor base material 71 that can adopt the laminated body according to the present embodiment corresponds to the optical member in the present embodiment. Since the touch sensor 70 having such a touch sensor base material 71 adopts the resin film or laminate according to the present embodiment, it is excellent in flexibility.

The front plate 90 is formed of a light-transmitting material. The front plate 90 is located on the outermost layer on the display screen side of the display device, and functions as a protective member for protecting the display device. The front plate is sometimes referred to as a window film. As the front plate 90, an inorganic material such as glass or a known transparent resin such as an acrylic resin can be used. As the front plate 90, the resin film or laminate according to the present embodiment described above can also be adopted. When a laminated body is adopted as the front plate 90, the laminated body is usually arranged so that the functional layer is located outside the display device.

Since the front plate 90 that can adopt the resin film or laminate according to the present embodiment adopts the resin film or laminate according to the present embodiment, it is excellent in flexibility.

When the display device 100 adopts the resin film or laminate according to the present embodiment as one or more constituent members selected from the organic EL device 50, the touch sensor 70, and the front plate 90, it has excellent flexibility as a whole. be able to. That is, the display device 100 can be a flexible device.

The device (flexible device) to which the resin film and the laminate according to the present embodiment can be applied is not limited to the above display device. For example, it can also be used in a solar cell having a substrate on which a photoelectric conversion element is formed and a front plate provided on the surface of the substrate. In this case, if the resin film or laminate according to the present embodiment is used as the substrate or front plate of the solar cell, the solar cell can have excellent flexibility as a whole.

Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples.

[Example 1]
The compound represented by the formula (1), the compound represented by the formula (2), the compound represented by the formula (3), the catalyst and the solvent (γ-butyrolactone and dimethylacetamide) were charged in the nitrogen-substituted polymerization tank. .. The amount charged was 75.0 g of the compound represented by the formula (1), 36.5 g of the compound represented by the formula (2), 76.4 g of the compound represented by the formula (3), 1.5 g of the catalyst, and γ-butyrolactone. It was 438.4 g and 313.1 g of dimethylacetamide. The molar ratio of the compound represented by the formula (2) to the compound represented by the formula (3) is 3: 7, and the total of the compound represented by the formula (2) and the compound represented by the formula (3). The molar ratio with the compound represented by the formula (1) was 1.00: 1.02.

After stirring the mixture in the polymerization tank to dissolve the raw material in the solvent, the temperature of the mixture was raised to 100 ° C., then the temperature was raised to 200 ° C., and the temperature was kept for 4 hours to polymerize the polyimide. During this heating, the water in the liquid was removed. Then, it was purified and dried to obtain polyimide.

Next, a γ-butyrolactone solution of polyimide adjusted to a concentration of 20% by mass, a dispersion liquid in which silica particles having a solid content concentration of 30% by mass are dispersed in γ-butyrolactone, a dimethylacetamide solution of alkoxysilane having an amino group, and triazine-based ultraviolet absorption. The agent (TINUVIN® 479, manufactured by BASF) and water were mixed and stirred for 30 minutes. These agitations were performed in accordance with the method described in US Pat. No. 6,207,256B2.

Here, the mass ratio of silica particles to polyimide is 60:40, the amount of alkoxysilane having an amino group is 1.67 parts by mass with respect to 100 parts by mass of the total of silica particles and polyimide, and the amount of triazine-based ultraviolet absorber is set. The amount of water was 3 parts by mass with respect to 100 parts by mass of the total of silica particles and polyimide, and the amount of water was 10 parts by mass with respect to 100 parts by mass of the total of silica particles and polyimide.

The mixed solution was applied to a glass substrate and heated at 50 ° C. for 30 minutes and 140 ° C. for 10 minutes to dry. Then, the film was peeled off from the glass substrate, a gold frame was attached, and the film was heated at 210 ° C. for 1 hour to obtain a resin film having a thickness of 80 μm. The content of silica particles in this resin film is 60% by mass.

[Example 2 (laminated body)]
A two-component curable primer (trade name: Alacoat AP2510, manufactured by Arakawa Chemical Industries, Ltd.) is applied as a primer layer to one surface of the resin film produced in Example 1 to form a coating film, and the coating film is formed. Was dried and cured to form a primer layer having a thickness of 1 μm.

Next, on the primer layer, 47.5 parts by mass of a tetrafunctional acrylate (trade name: A-TMMT, manufactured by Shin-Nakamura Chemical Co., Ltd.) and a trifunctional acrylate (trade name: A-TMPT, manufactured by Shin-Nakamura Chemical Co., Ltd.) 47. 5 parts by mass, reactive urethane polymer (trade name: 8BR-600, manufactured by Taisei Fine Chemicals, 40% by mass) 12.5 parts by mass, triazine-based ultraviolet absorber (TINUVIN (registered trademark) 479, manufactured by BASF) 3 By mass, 8 parts by mass of photopolymerization initiator (IRGACURE (registered trademark) 184, manufactured by Ciba Specialty Chemicals), 0.6 parts by mass of leveling agent (trade name: BYK-350, manufactured by Big Chemie Japan), and methyl ethyl ketone 107. A coating film was formed by applying a solution prepared by mixing parts by mass. The coating film was dried and cured to form a functional layer having a thickness of 10 μm as a “functional layer having a function of developing high hardness on the surface and a function of absorbing ultraviolet rays” to obtain a laminate of Example 2. ..

[Comparative Example 1]
A resin film having a thickness of 80 μm was obtained in the same manner as in Example 1 except that the triazine-based ultraviolet absorber was not added to the mixed solution for forming the resin film.

[Comparative Example 2]
A polyimide having a glass transition temperature of 390 ° C. (“Neoprim” manufactured by Mitsubishi Gas Chemical Company, Inc.) was prepared. A γ-butyrolactone solution having a concentration of 20% by mass of this polyimide, a dispersion liquid in which silica particles having a solid content concentration of 30% by mass are dispersed in γ-butyrolactone, a dimethylacetamide solution of alkoxysilane having an amino group, and water are mixed for 30 minutes. The mixture was stirred to obtain a mixed solution. The mass ratio of silica particles to polyimide is 55:45, the amount of alkoxysilane having an amino group is 1.67 parts by mass with respect to 100 parts by mass of the total of silica particles and polyimide, and the amount of water is that of silica particles and polyimide. It was 10 parts by mass with respect to 100 parts by mass in total. Using this mixed solution, a resin film having a thickness of 80 μm was obtained in the same manner as in Example 1.

(evaluation)
1) Optical characteristics (yellowness (YI value))
The yellowness (Yellow Index: YI value) of each of the resin films of Examples and Comparative Examples was measured by an ultraviolet-visible near-infrared spectrophotometer V-670 manufactured by JASCO Corporation. After performing background measurement in the absence of a sample, a resin film was set in a sample holder, transmittance was measured for light of 300 nm to 800 nm, and tristimulation values (X, Y, Z) were determined. The YI value was calculated based on the following formula.
YI = 100 × (1.2769X-1.592Z) / Y

2) Transmittance Using an ultraviolet-visible near-infrared spectrophotometer V-670 manufactured by JASCO Corporation, the transmittance for light of 300 nm to 800 nm was measured, and the transmittance for light having a wavelength of 550 nm was calculated.

3) Haze Using a fully automatic direct reading haze computer HGM-2DP manufactured by Suga Test Instruments Co., Ltd., the resin films of Examples and Comparative Examples were set in the sample holder, and the haze of the resin film was measured.

4) Light Irradiation Test The resin films of Examples and Comparative Examples were subjected to a light irradiation test using UVCON manufactured by Atras. The light source was UV-B 313 nm, the output was 40 W, and the distance between the resin film and the light source was set to 5 cm. The resin film was irradiated with ultraviolet rays for 24 hours. After irradiation with ultraviolet rays, the optical characteristics (YI value, transmittance) were evaluated as described above.

5) Visibility The film before the light irradiation test was bent, the appearance state such as contrast and hue at that time was confirmed, and the visibility was judged according to the following criteria.
A: No change in contrast or hue is observed.
C: Appearance changes such as changes in contrast and hue were observed.

Table 1 shows the evaluation results. It was confirmed that the resin film of the example subjected to the light irradiation test satisfied the above-mentioned conditions (i) and (ii), and that the resin film and the laminate having the same had high visibility at the time of bending. Was done.

10 ... resin film, 20 ... functional layer, 25 ... primer layer, 30 ... laminated body (laminated body), 50 ... organic EL device, 70 ... touch sensor, 90 ... front plate, 100 ... display device.

Claims (4)

A front plate of a flexible device having a resin film containing a polyimide-based polymer.
The resin film further contains an ultraviolet absorber and
The polyimide-based polymer is a polymer having at least a repeating structural unit represented by the formula (PI), and the structural unit represented by the formula (PI) is relative to all the repeating structural units of the polyimide-based polymer. 40 mol% or more,

[In the formula (PI), G is a group represented by the formula (20), the formula (21), the formula (22), the formula (23), the formula (24), the formula (25) and the formula (26), respectively. It is one of the groups selected from the group consisting of
In equations (20) to (26), * represents a bond and represents a bond.
Z in the formula (26) is a single bond, -O-, -CH _2- , -C (CH ₃ ) _2- , -Ar-O-Ar-, -Ar-CH ₂ -Ar-, -Ar- C (CH ₃ ) represents ₂ -Ar- or -Ar-SO ₂ -Ar-, where Ar represents an aryl group having 6 to 20 carbon atoms (at least one of the hydrogen atoms of these groups is a fluorine-based substitution). May be substituted with a group),

A is any group selected from the group consisting of the groups represented by the following formulas (30), formula (31), formula (32), formula (33) and formula (34), respectively.
In equations (30) to (34), * represents a bond and represents a bond.
In formula (32), Z ¹ is a single bond, -O-, -CH _2- , -C (CH ₃ ) _2- , -SO _2- , -CO- or -CO-NR- (R is the number of carbon atoms). Represents 1 to 3 alkyl groups or hydrogen atoms)
In formula (33), Z ¹ and Z ² are independently single-bonded, -O-, -CH _2- , -C (CH ₃ ) _2- , -SO _2- , -CO- or -CO. -NR- (R represents an alkyl group or a hydrogen atom having 1 to 3 carbon atoms),
Fluorine-based substituents may be introduced into the groups represented by the formulas (30), (31), (32) and (33).
In formula (34), Z ¹ and Z ³ are independently single-bonded, -O-, -CH _2- , -C (CH ₃ ) _2- , -SO _2- , -CO- or -CO. -NR- (R represents an alkyl group or a hydrogen atom having 1 to 3 carbon atoms), Z ² is a single bond, -CH _2- , -C (CH ₃ ) _2- , -SO ₂ -,- Represents CO- or -CO-NR- (R represents an alkyl group or hydrogen atom having 1 to 3 carbon atoms).

When a light irradiation test was conducted in which the resin film was irradiated with light of 313 nm from one surface of the resin film for 24 hours by a light source having an output of 40 W provided at a distance of 5 cm from the resin film, the resin film was as follows. conditions:
(I) The resin film after the light irradiation test has a transmittance of 85% or more with respect to light of 550 nm, and
(Ii) The resin film before the light irradiation test has a yellowness of 5 or less, and the difference in yellowness before and after the light irradiation test of the resin film is less than 2.5.
The filling,
The resin film after the light irradiation test has a haze of 0.8% or less.
Front plate of flexible device. The front plate of a flexible device according to claim 1 , further comprising a laminate having the resin film and a functional layer provided on at least one surface side of the resin film. The front plate of a flexible device according to claim 2 , wherein the functional layer is a layer having at least one function selected from the group consisting of a function of absorbing ultraviolet rays, adhesiveness, and a function of exhibiting high hardness on the surface. The front plate of the flexible device according to claim 2 or 3 , further comprising a primer layer provided between the resin film and the functional layer.

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