JP7087162B2 - Adhesive sheet - Google Patents

Description

The present invention relates to an adhesive sheet.

In general, a pressure-sensitive adhesive (also referred to as a pressure-sensitive adhesive; the same applies hereinafter) exhibits a soft solid state (viscous elastic body) in a temperature range near room temperature, and has a property of easily adhering to an adherend by pressure. Taking advantage of such properties, adhesives are widely used in various applications for the purpose of joining, fixing, and protecting members in portable electronic devices such as mobile phones. For example, an adhesive having a light-shielding adhesive layer for the purpose of preventing light leakage from a light source such as a backlight module of a liquid crystal display device in a portable electronic device such as a mobile phone or a self-luminous element such as organic EL (electroluminescence). Sheets are used. Further, for the purpose of concealing the adherend, adjusting the appearance of the adherend through the adhesive sheet (for example, suppressing appearance unevenness), designability, etc., an adhesive sheet having a predetermined light-shielding property and dimming property is used. Patent Document 1 is mentioned as a document relating to this kind of technique.

Japanese Unexamined Patent Publication No. 2020-37657

In the pressure-sensitive adhesive sheet having limited light transmission as described above, the pressure-sensitive adhesive sheet absorbs light, thereby controlling the light. However, even in such a pressure-sensitive adhesive sheet with limited light transmission, it may be difficult to realize more accurate optical control because the light that has entered the pressure-sensitive adhesive is refracted and scattered in the pressure-sensitive adhesive. .. For example, in various devices such as the portable electronic devices described above, light rays such as infrared rays, visible light, and ultraviolet rays are emitted for the purpose of operating the devices, detecting nearby objects, detecting the ambient brightness (ambient light), and data communication. The used optical sensor is used. The refraction of light rays used in an optical sensor, and the ingress, refraction, and scattering of light rays from outside the device may affect the operating accuracy of the sensor or cause a poor response of the sensor. If the light transmission can be limited and the influence of the light entering the pressure-sensitive adhesive can be reduced, it is possible to achieve both light-shielding property and dimming property and high-precision optical control, which is significant.

According to the present invention, there is provided a pressure-sensitive adhesive composition containing one or more of the components that may be contained in the pressure-sensitive adhesive layer disclosed herein. The pressure-sensitive adhesive composition is a pressure-sensitive adhesive composition used for bonding members of portable electronic devices, and contains an acrylic polymer as a base polymer and at least two kinds of colorants. The base polymer 100 is a tackifier resin containing a black colorant as a first colorant, having a content of the black colorant of 0.6% by weight or less based on a solid content and a softening point of 80 ° C. or higher. It is a pressure-sensitive adhesive composition containing 1 to 20 parts by weight with respect to parts by weight.

The pressure-sensitive adhesive sheet disclosed herein can be preferably used for joining members of a portable electronic device. For example, since the portable electronic device may have a built-in optical sensor, it is possible to reduce the influence on the operation of the optical sensor by performing optical control using the adhesive sheet disclosed herein. Further, as described above, the portable electronic device is required to prevent light leakage if it has a light source. In addition, it may be required to conceal the adherend or impart design. Therefore, it is particularly meaningful to apply the technique disclosed herein to perform optical control by suppressing the light entering the pressure-sensitive adhesive while limiting the light transmission.

It is sectional drawing which shows typically one structural example of the pressure-sensitive adhesive sheet. It is sectional drawing which shows typically one structural example of a laminated body. It is an exploded perspective view which shows the structural example of the display device schematically.

Hereinafter, preferred embodiments of the present invention will be described. Matters other than those specifically mentioned in the present specification and necessary for the implementation of the present invention are based on the teachings regarding the implementation of the invention described in the present specification and the common general knowledge at the time of filing. Can be understood by those skilled in the art. The present invention can be carried out based on the contents disclosed in the present specification and the common general technical knowledge in the art. Further, in the following drawings, members / parts having the same function may be described with the same reference numerals, and duplicate description may be omitted or simplified. Further, the embodiments described in the drawings are schematicized for clearly explaining the present invention, and do not necessarily accurately represent the size and scale of the pressure-sensitive adhesive sheet of the present invention actually provided as a product. ..

As described above, the term "adhesive" as used herein refers to a material that exhibits a soft solid state (viscoelastic body) in a temperature range near room temperature and has the property of easily adhering to an adherend by pressure. .. The pressure-sensitive adhesive here is generally defined as "CA Dahlquist," Adhesion: Fundamental and Practice ", McLaren & Sons, (1966) P. 143", and generally has a complex tensile modulus E ^* (1 Hz). It can be a material having a property of satisfying < ¹⁰⁷ dyne / cm ² (typically, a material having the above-mentioned property at 25 ° C.).

<Structure example of adhesive sheet>
The pressure-sensitive adhesive sheet disclosed herein may be a pressure-sensitive adhesive sheet with a base material having the pressure-sensitive adhesive layer on one side or both sides of a non-peelable base material (supporting base material), and the pressure-sensitive adhesive layer may be peeled off. It may be a base material-less pressure-sensitive adhesive sheet (that is, a pressure-sensitive adhesive sheet having no non-peelable base material) such as a form held on a liner. The concept of the pressure-sensitive adhesive sheet as used herein may include what is called an pressure-sensitive adhesive tape, a pressure-sensitive adhesive label, a pressure-sensitive adhesive film, or the like. The pressure-sensitive adhesive sheet disclosed herein may be in the form of a roll or in the form of a single leaf. Alternatively, the pressure-sensitive adhesive sheet may be further processed into various shapes.

FIG. 1 shows a configuration example of a double-sided adhesive type base material-less adhesive sheet (base material-less double-sided adhesive sheet). In the pressure-sensitive adhesive sheet 1 shown in FIG. 1, both sides 21A and 21B of the pressure-sensitive adhesive layer 21 without a base material (which are also the pressure-sensitive adhesive surfaces 1A and 1B of the pressure-sensitive adhesive sheet 1 respectively) have at least the pressure-sensitive adhesive layer side as a peeling surface. It has a structure protected by the release liners 31 and 32, respectively. Alternatively, the adhesive sheet has a structure in which one surface (adhesive surface, first adhesive surface) of the adhesive layer without a base material is protected by a release liner having both sides as release surfaces, and the adhesive sheet is wound. When turned, the other surface (adhesive surface, second adhesive surface) of the adhesive layer comes into contact with the back surface of the release liner, so that the second adhesive surface of the adhesive layer is also protected by the release liner. You may be able to do it. The technique disclosed herein can be preferably carried out in such a substrate-less form from the viewpoint of reducing the thickness of the pressure-sensitive adhesive sheet. The base material-less pressure-sensitive adhesive sheet is also advantageous in that it is easy to form a thin layer and can maximize the pressure-sensitive adhesive properties such as adhesive strength and impact resistance. As will be described later, the pressure-sensitive adhesive layer 21 contains at least two kinds of colorants, and the light transmittance is limited to 30% or less.

<Characteristics of adhesive layer>
(Light transmittance)
The pressure-sensitive adhesive layer constituting the pressure-sensitive adhesive sheet disclosed herein has a light transmittance of 30% or less. The pressure-sensitive adhesive sheet having such a pressure-sensitive adhesive layer can have a light-shielding property suitable for preventing light leakage. Further, it is suitable for concealing the adherend and adjusting the appearance of the adherend through the adhesive sheet (for example, suppressing uneven appearance), and can impart designability. The light transmittance of the pressure-sensitive adhesive layer is preferably 28% or less , more preferably 25% or less, still more preferably 20% or less, and may be 18% or less, and in some preferred embodiments, the pressure-sensitive adhesive layer. The light transmittance of is less than 12%, may be less than 10%, may be less than 8.0%, may be less than 6.0%, may be less than 4.0%, may be less than 3.0%. good. The lower the light transmittance, the better the light-shielding property and the hiding property. The lower limit of the light transmittance is not particularly limited, and may be substantially 0%, that is, may be equal to or less than the detection limit, and may be 0.05% or more from the viewpoint of compatibility with the light reflectance described later. , 0.1% or more, 1.0% or more, 2.0% or more, 5.0% or more. In some embodiments, the light transmittance of the pressure-sensitive adhesive layer is 8.0% or more, and may be 12% or more (for example, 15% or more). By having a certain degree of light transmittance, it is possible to appropriately conceal the adherend, adjust the appearance of the adherend (for example, a metal material), and impart a design that retains the texture of the adherend. can. A pressure-sensitive adhesive layer having moderate light transmission is preferable from the viewpoint of maintaining the pressure-sensitive adhesive properties, productivity, and the like.

The light transmittance of the pressure-sensitive adhesive layer can be measured by the method described in Examples described later. The light transmittance of the pressure-sensitive adhesive layer can be adjusted by adjusting the pressure-sensitive adhesive-containing component (for example, the type and amount of a colorant (preferably a black colorant)), the thickness of the pressure-sensitive adhesive layer, and the like.

(Light reflectance)
The light reflectance of the pressure-sensitive adhesive layer is 8.0% or more. The pressure-sensitive adhesive layer having a limited light transmittance as described above has a limited amount of light input, but even in such a pressure-sensitive adhesive layer, the light that has entered the pressure-sensitive adhesive is refracted and scattered in the pressure-sensitive adhesive. Therefore, it may be difficult to realize more accurate optical control. In addition to limiting the light transmittance of the pressure-sensitive adhesive layer, the light transmittance on the surface of the pressure-sensitive adhesive layer is set to 8% or more to reflect light on the pressure-sensitive adhesive surface and reduce the light entering the pressure-sensitive adhesive. It is possible to achieve both light-shielding and dimming properties and high-precision optical control. The light reflectance of the pressure-sensitive adhesive layer is preferably 9.0% or more, more preferably 10% or more, still more preferably 12% or more, and may be 14% or more (for example, 16% or more). Since the upper limit of the light reflectance is set in an appropriate range in relation to the light transmittance, it is not limited to a specific range, for example, it is less than 40%, may be 30% or less, and may be 20%. It may be less than or equal to (for example, 15% or less).

The light reflectance of the pressure-sensitive adhesive layer can be measured by the method described in Examples described later. The light reflectance of the pressure-sensitive adhesive layer can be adjusted by the pressure-sensitive adhesive-containing component (for example, the type and amount of a colorant (preferably a metal oxide)).

In the case of a double-sided adhesive sheet having adhesive surfaces on both sides, the light reflectance of each adhesive layer surface (each adhesive surface; the first adhesive surface and the second adhesive surface) may be the same or different. In an embodiment in which the light reflectance of each pressure-sensitive adhesive layer surface (each pressure-sensitive adhesive surface) of the double-sided pressure-sensitive adhesive sheet is different, one pressure-sensitive adhesive layer surface (for example, the first pressure-sensitive adhesive surface) may have the above-mentioned light reflectance, and the other. The light reflectance of the surface of the pressure-sensitive adhesive layer (for example, the second pressure-sensitive adhesive surface) may be less than 8%.

The relative relationship between the light transmittance and the light reflectance of the pressure-sensitive adhesive layer is not particularly limited, and is appropriately set so as to have a better balance between the reduction of light transmittance and the reduction of the amount of light entering the pressure-sensitive adhesive layer. Can be done. For example, the ratio (R / T) of the light reflectance R to the light transmittance T of the pressure-sensitive adhesive layer is preferably 0.4 or more, preferably 0.5 or more, more preferably 1.0 or more. It is more preferably 2.0 or more, and particularly preferably 4.0 or more (for example, 4.5 or more). Further, the upper limit of the ratio (R / T) is about 10 or less, and may be, for example, 5 or less. In an embodiment in which the pressure-sensitive adhesive layer is required to have a certain degree of light transmission, the ratio (R / T) may be less than 3, may be less than 2, or may be less than 1.

<Adhesive layer>
(Base polymer)
In the technique disclosed herein, the type of the pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer is not particularly limited. The pressure-sensitive adhesives include acrylic polymers, rubber-based polymers (natural rubber, synthetic rubber, mixtures thereof, etc.), polyester-based polymers, urethane-based polymers, polyether polymers, silicone-based polymers, which can be used in the field of pressure-sensitive adhesives. One or more of various rubber-like polymers such as polyamide-based polymers and fluoropolymers may be contained as an adhesive polymer (hereinafter, also referred to as "base polymer" in the sense of a structural polymer forming an adhesive). .. From the viewpoint of adhesive performance, cost, and the like, a pressure-sensitive adhesive containing an acrylic polymer or a rubber-based polymer as a base polymer can be preferably adopted. Of these, a pressure-sensitive adhesive (acrylic pressure-sensitive adhesive) using an acrylic polymer as a base polymer is preferable. The technique disclosed herein is preferably carried out in an embodiment using an acrylic pressure-sensitive adhesive.

Hereinafter, the pressure-sensitive adhesive layer composed of the acrylic pressure-sensitive adhesive, that is, the pressure-sensitive adhesive sheet having the acrylic-based pressure-sensitive adhesive layer will be mainly described, but the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet disclosed herein is composed of the acrylic pressure-sensitive adhesive. It is not intended to be limited to acrylic.

The "base polymer" of the pressure-sensitive adhesive refers to the main component of the rubber-like polymer contained in the pressure-sensitive adhesive, and is not interpreted in a limited manner other than this. The rubber-like polymer refers to a polymer that exhibits rubber elasticity in a temperature range near room temperature. Further, in this specification, the “main component” refers to a component contained in an amount of more than 50% by weight, unless otherwise specified.
Further, the "acrylic polymer" refers to a polymer containing a monomer unit derived from a monomer having at least one (meth) acryloyl group in one molecule as a monomer unit constituting the polymer. Hereinafter, a monomer having at least one (meth) acryloyl group in one molecule is also referred to as an “acrylic monomer”. Therefore, the acrylic polymer in this specification is defined as a polymer containing a monomer unit derived from an acrylic monomer. A typical example of the acrylic polymer is an acrylic polymer in which the proportion of the acrylic monomer in the total monomer components used in the synthesis of the acrylic polymer is more than 50% by weight.
In addition, "(meth) acryloyl" means acryloyl and methacryloyl comprehensively. Similarly, "(meth) acrylate" means acrylate and methacrylate, and "(meth) acrylic" means acrylic and methacrylic, respectively.

(Acrylic polymer)
As the acrylic polymer in the technique disclosed herein, for example, a polymer of a monomer raw material containing an alkyl (meth) acrylate as a main monomer and further containing a submonomer having copolymerizability with the main monomer is preferable. Here, the main monomer means a component that occupies more than 50% by weight of the monomer composition in the above-mentioned monomer raw material.

As the alkyl (meth) acrylate, for example, a compound represented by the following formula (1) can be preferably used.
CH ₂ = C (R ¹ ) COOR ² (1)
Here, R ¹ in the above formula (1) is a hydrogen atom or a methyl group. Further, R ² is a chain alkyl group having 1 to 20 carbon atoms. Hereinafter, such a range of the number of carbon atoms may be expressed as "C _1-20 ". From the viewpoint of the storage elastic modulus of the pressure-sensitive adhesive, the main monomer is an alkyl (meth) acrylate in which R ² is a chain alkyl group of C _1-14 (for example, C _1-10 , typically C _4-8 ). It is appropriate to do. From the viewpoint of adhesive properties, the main monomer is an alkyl acrylate in which R ¹ is a hydrogen atom and R ² is a chain alkyl group of C _4-8 (hereinafter, also simply referred to as C _4-8 alkyl acrylate). Is preferable.

Specific examples of the alkyl (meth) acrylate in which R ² is a C _1-20 chain alkyl group are not particularly limited, but are, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, and isopropyl. (Meta) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, pentyl (meth) acrylate, isopentyl (meth) acrylate, hexyl (meth) ) Acrylate, Heptyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, isooctyl (meth) acrylate, nonyl (meth) acrylate, isononyl (meth) acrylate, decyl (meth) acrylate, isodecyl (meth) ) Acrylate, undecyl (meth) acrylate, dodecyl (meth) acrylate, tridecyl (meth) acrylate, tetradecyl (meth) acrylate, pentadecyl (meth) acrylate, hexadecyl (meth) acrylate, heptadecyl (meth) acrylate, octadecyl (meth) acrylate. , Nonadecil (meth) acrylate, Eikosyl (meth) acrylate and the like. These alkyl (meth) acrylates can be used alone or in combination of two or more. Preferable examples of alkyl (meth) acrylates include n-butyl acrylate (BA) and 2-ethylhexyl acrylate (2EHA).

The proportion of alkyl (meth) acrylate in the monomer component constituting the acrylic polymer is typically more than 50% by weight, for example, 70% by weight or more, 85% by weight or more, and 90% by weight. It may be% by weight or more. The upper limit of the proportion of the alkyl (meth) acrylate is not particularly limited, but is preferably 99.5% by weight or less (for example, 99% by weight or less), or characteristics based on an accessory monomer such as a carboxy group-containing monomer (for example, agglomeration). From the viewpoint of preferably exerting force), it may be 98% by weight or less (for example, less than 97% by weight). Alternatively, the acrylic polymer may be substantially obtained by polymerizing only an alkyl (meth) acrylate.

When C _4-8 alkyl acrylate is used as the monomer component, the proportion of C _4-8 alkyl acrylate in the alkyl (meth) acrylate contained in the monomer component is preferably 70% by weight or more. More preferably, it is 90% by weight or more.

The acrylic polymer in the technique disclosed herein may be copolymerized with a submonomer. A carboxy group-containing monomer, a hydroxyl group (OH group) -containing monomer, an acid anhydride group-containing monomer, and an amide group-containing as an auxiliary monomer that can introduce a functional group that can serve as a cross-linking base point into an acrylic polymer or contribute to an improvement in adhesive strength. Examples thereof include a monomer, an amino group-containing monomer, an epoxy group-containing monomer, a cyano group-containing monomer, a keto group-containing monomer, a monomer having a nitrogen atom-containing ring, an alkoxysilyl group-containing monomer, and an imide group-containing monomer. As the submonomer, one type may be used alone or two or more types may be used in combination.
As a preferred example of the acrylic polymer in the technique disclosed herein, an acrylic polymer obtained by copolymerizing a carboxy group-containing monomer as the submonomer can be mentioned. Examples of the carboxy group-containing monomer include acrylic acid (AA), methacrylic acid (MAA), carboxyethyl (meth) acrylate, carboxypentyl (meth) acrylate, itaconic acid, maleic acid, fumaric acid, crotonic acid, and isocrotonic acid. Will be done. Of these, AA and MAA are preferable.
As another preferable example, an acrylic polymer obtained by copolymerizing a hydroxyl group-containing monomer as the submonomer can be mentioned. Examples of hydroxyl group-containing monomers include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and 4-hydroxybutyl (meth). ) Hydroxyalkyl (meth) acrylates such as acrylates; polypropylene glycol mono (meth) acrylates; N-hydroxyethyl (meth) acrylamides and the like. Among them, preferred examples of the hydroxyl group-containing monomer include hydroxyalkyl (meth) acrylates in which the alkyl group is linear with 2 to 4 carbon atoms.

When the monomer component constituting the acrylic polymer contains the above-mentioned functional group-containing monomer, the content of the functional group-containing monomer in the monomer component is not particularly limited. From the viewpoint of appropriately exerting the effect of using the functional group-containing monomer, the content of the functional group-containing monomer in the monomer component can be, for example, 0.1% by weight or more, and 0.5% by weight or more. Is appropriate, and may be 1% by weight or more. Further, from the viewpoint of facilitating the balance of adhesive performance in relation to the main monomer, it is appropriate that the content of the functional group-containing monomer in the monomer component is 40% by weight or less, and 20% by weight or less. Is preferable, and it may be 10% by weight or less (for example, 5% by weight or less).

In the base polymer according to some preferred embodiments, the monomer component constituting the base polymer (for example, an acrylic polymer) may contain a carboxy group-containing monomer. When the monomer component contains a carboxy group-containing monomer, it becomes easy to obtain a pressure-sensitive adhesive sheet exhibiting good pressure-sensitive adhesive properties (cohesive force, etc.). In addition, it may be advantageous to improve the adhesion between the pressure-sensitive adhesive layer and the adherend. Further, by copolymerizing an appropriate amount of a carboxy group-containing monomer, even when a black colorant such as carbon black is blended in the pressure-sensitive adhesive, the colorant can be easily dispersed in the layer and the pressure-sensitive adhesive property can be improved. It can be preferably maintained.

In the embodiment in which the carboxy group-containing monomer is copolymerized with the base polymer, the content of the carboxy group-containing monomer in the monomer component constituting the base polymer is not particularly limited, and is, for example, 0.2% by weight or more of the monomer component. It can be (typically 0.5% by weight or more), 1% by weight or more is appropriate, and 2% by weight or more may be used, or 3% by weight or more may be used. A higher effect is exhibited by setting the content of the carboxy group-containing monomer to more than 3% by weight. In some embodiments, the content of the carboxy group-containing monomer can be 3.2% by weight or more of the monomer component, 3.5% by weight or more, or 4% by weight or more. It may be 5% by weight or more. The upper limit of the content of the carboxy group-containing monomer is not particularly limited, and may be, for example, 15% by weight or less, 12% by weight or less, or 10% by weight or less. The techniques disclosed herein have a carboxy group-containing monomer content of 7% by weight or less of the monomer component (typically less than 7% by weight, such as 6.8% by weight or less, or 6.0% by weight or less). It can also be preferably carried out in certain embodiments.

The monomer component constituting the acrylic polymer may contain a copolymerization component other than the above-mentioned submonomer for the purpose of improving the cohesive force and the like. Examples of other copolymerization components include vinyl ester-based monomers such as vinyl acetate, vinyl propionate, vinyl laurate; aromatic vinyl compounds such as styrene, substituted styrene (α-methylstyrene, etc.), vinyl toluene; cyclohexyl (cyclohexyl). Cycloalkyl (meth) acrylates such as meta) acrylates, cyclopentyl (meth) acrylates, isobornyl (meth) acrylates; aryl (meth) acrylates (eg phenyl (meth) acrylates), aryloxyalkyl (meth) acrylates (eg phenoxyethyl (eg phenoxyethyl) Aromatic ring-containing (meth) acrylates such as (meth) acrylates) and arylalkyl (meth) acrylates (eg, benzyl (meth) acrylates); olefinic monomers such as ethylene, propylene, isoprene, butadiene, and isobutylene; vinyl chloride, chloride. Chlorine-containing monomers such as vinylidene; isocyanate group-containing monomers such as 2- (meth) acryloyloxyethyl isocyanate; alkoxy group-containing monomers such as methoxyethyl (meth) acrylate and ethoxyethyl (meth) acrylate; Vinyl ether-based monomer; 2 or more (for example, 3 or more) polymerizable functional groups (for example, (meth) acryloyl group) in one molecule such as 1,6-hexanediol di (meth) acrylate and trimethyl propantri (meth) acrylate. ), And the like.

The amount of the other copolymerization component may be appropriately selected depending on the purpose and application, and is not particularly limited, but is appropriately set to 0.05% by weight or more from the viewpoint of appropriately exerting the effect of use. , 0.5% by weight or more may be used. Further, from the viewpoint of facilitating the balance of adhesive performance, it is appropriate that the content of the other copolymerization component in the monomer component is 20% by weight or less, and 10% by weight or less (for example, 5% by weight or less). May be good. The technique disclosed herein may also be preferably carried out in an embodiment in which the monomer component is substantially free of other copolymerization components. Here, the fact that the monomer component does not substantially contain other copolymerization components means that the other copolymerization components are not used at least intentionally, and the other copolymerization components are, for example, 0.01% by weight or less. To some extent, unintentional inclusion is acceptable.

It is appropriate that the copolymerization composition of the acrylic polymer is designed so that the glass transition temperature (Tg) of the polymer is about −15 ° C. or lower (for example, about −70 ° C. or higher and −15 ° C. or lower). Here, the Tg of the acrylic polymer means the Tg obtained by the Fox formula based on the composition of the monomer component used for the synthesis of the polymer. As shown below, the Fox formula is a relational formula between the Tg of the copolymer and the glass transition temperature Tgi of the homopolymer obtained by homopolymerizing each of the monomers constituting the copolymer.
1 / Tg = Σ (Wi / Tgi)
In the above Fox formula, Tg is the glass transition temperature (unit: K) of the copolymer, Wi is the weight fraction of the monomer i in the copolymer (copolymerization ratio based on the weight), and Tgi is the monomer i. Represents the glass transition temperature (unit: K) of the homopolymer.

As the glass transition temperature of the homopolymer used for calculating Tg, the numerical values described in publicly known materials, specifically, "Polymer Handbook" (3rd edition, John Wiley & Sons, Inc., 1989) shall be used. .. For monomers for which multiple types of values are described in this document, the highest value is adopted. If it is not described in the Polymer Handbook, the value obtained by the measuring method described in JP-A-2007-51271 shall be used.

Although not particularly limited, it is advantageous that the Tg of the acrylic polymer is about −25 ° C. or lower, preferably about −35 ° C. or lower, from the viewpoint of impact resistance and adhesion to the adherend. , More preferably about −40 ° C. or lower. In some embodiments, from the viewpoint of cohesive force, the Tg of the acrylic polymer is, for example, about −70 ° C. or higher, may be about −65 ° C. or higher, may be about −60 ° C. or higher, or may be about −55 ° C. or higher. good. The technique disclosed herein can be preferably carried out in an embodiment in which the Tg of the acrylic polymer is approximately −65 ° C. or higher and −35 ° C. or lower (for example, approximately −55 ° C. or higher and −40 ° C. or lower). The Tg of the acrylic polymer can be adjusted by appropriately changing the monomer composition (that is, the type and amount ratio of the monomers used in the synthesis of the polymer).

The method for obtaining the acrylic polymer is not particularly limited, and various polymerization methods known as synthetic methods for the acrylic polymer, such as a solution polymerization method, an emulsion polymerization method, a bulk polymerization method, a suspension polymerization method, and a photopolymerization method. Can be adopted as appropriate. For example, a solution polymerization method can be preferably adopted. The polymerization temperature at the time of solution polymerization can be appropriately selected depending on the type of the monomer and solvent used, the type of the polymerization initiator and the like, and is, for example, about 20 ° C. to 170 ° C. (typically 40 ° C. to 140 ° C.). ℃).

The solvent (polymerization solvent) used for solution polymerization can be appropriately selected from conventionally known organic solvents (toluene, ethyl acetate, etc.). The initiator used for the polymerization may be an azo-based polymerization initiator such as a conventionally known polymerization initiator (for example, 2,2'-azobisisobutyronitrile (AIBN)) or a peroxide-based initiator, depending on the type of the polymerization method. It can be appropriately selected from the initiator, etc.). The amount of the polymerization initiator used may be a normal amount, for example, about 0.005 to 1 part by weight (typically about 0.01 to 1 part by weight) with respect to 100 parts by weight of the monomer component. ) Can be selected.

The weight average molecular weight (Mw) of the base polymer (preferably an acrylic polymer) in the technique disclosed herein is not particularly limited and may be, for example, in the range of approximately 10 × 10 ⁴ to 500 × 10 ⁴ . From the viewpoint of adhesive performance, the Mw of the base polymer is approximately 30 × 10 ⁴ to 200 × 10 ⁴ (more preferably approximately 45 × 10 ⁴ to 150 × 10 ⁴ , typically approximately 65 × 10 ⁴ to 130 × 10). It is preferably in the range of ⁴ ). By using a base polymer having a high Mw, it tends to be easy to obtain better impact resistance by utilizing the cohesive force of the polymer itself. Here, Mw means a value in terms of standard polystyrene obtained by GPC (gel permeation chromatography). As the GPC apparatus, for example, a model name “HLC-8320GPC” (column: TSKgelGMH-H (S), manufactured by Tosoh Corporation) can be used.

(Colorant)
The pressure-sensitive adhesive layer disclosed herein contains at least two types of colorants (first colorant and second colorant). By using two or more kinds of colorants, a pressure-sensitive adhesive layer satisfying a light transmittance of 30% or less and a light reflectance of 8% or more can be preferably realized. As the colorant, various materials that can be attenuated by absorbing light traveling in the pressure-sensitive adhesive layer and various materials that can reduce the amount of light entering the pressure-sensitive adhesive layer can be used. The colorant can be, for example, a colorant such as black, gray, white, red, blue, yellow, green, yellowish green, orange, purple, gold, silver, or pearl. The colorant can be typically contained in the pressure-sensitive adhesive layer in a dispersed state (may be in a dissolved state) in the constituent material of the pressure-sensitive adhesive layer. Conventionally known pigments and dyes can be used as the colorant. Examples of the pigment include inorganic pigments and organic pigments.

(First colorant)
The first colorant contained in the pressure-sensitive adhesive layer is not particularly limited, but is, for example, a component capable of absorbing and attenuating light traveling in the pressure-sensitive adhesive layer, and the colorant is contained in the pressure-sensitive adhesive layer. By doing so, it can be a component that reduces the light transmittance of the pressure-sensitive adhesive layer (hence, also referred to as a “light transmittance reducing component”). As such a first colorant, a black colorant can be preferably used because the light-shielding property can be efficiently adjusted with a small amount of the colorant. Specific examples of the black colorant include carbon black, graphite, aniline black, perylene black, cyanine black, titanium black, inorganic pigment hematite, activated carbon, molybdenum disulfide, chromium complex, anthraquinone-based colorant and the like. As the black colorant, one kind may be used alone or two or more kinds may be used in combination as appropriate.

In some preferred embodiments, the pressure-sensitive adhesive layer comprises carbon black particles as the first colorant. As the carbon black particles used, those generally called carbon black (furness black, channel black, acetylene black, thermal black, lamp black, pine smoke, etc.) can be used without particular limitation. Further, as the carbon black particles, it is also possible to use surface-modified carbon black particles having a functional group such as a carboxyl group, an amino group, a sulfonic acid group and a silicon-containing group (for example, an alkoxysilyl group and an alkylsilyl group). Such surface-modified carbon black particles are also referred to as self-dispersion type carbon black, and the addition of a dispersant becomes unnecessary or the addition amount thereof can be reduced. The carbon black particles may be used alone or in combination of two or more.

Since the light-shielding property of the pressure-sensitive adhesive layer can be efficiently adjusted with a small amount of the colorant, a particulate colorant (pigment) can be preferably used. In some preferred embodiments, a colorant having an average particle size of about 10 nm or more (for example, about 30 nm or more) (for example, a particulate black colorant such as carbon black) can be used. The average particle size is, for example, about 50 nm or more, may be about 100 nm or more, or may be about 150 nm or more. The upper limit of the average particle size of the colorant is not particularly limited, and may be, for example, about 3000 nm or less, and may be about 1000 nm or less. From the viewpoint of improving the light-shielding property, the average particle size of the colorant is preferably about 500 nm or less, preferably about 300 nm or less, more preferably about 250 nm or less, still more preferably 200 nm or less (for example, about 120 nm or less, further. Approximately 100 nm or less).

The average particle size of the colorant in the present specification refers to a volume average particle size, and specifically, an integrated value of 50% in the particle size distribution measured by a particle size distribution measuring device based on a laser scattering / diffraction method. (50% volume average particle size; hereinafter, it may be abbreviated as _D50 ). As the measuring device, for example, the product name “Microtrack MT3000II” manufactured by Microtrack Bell Co., Ltd. or an equivalent product thereof can be used.

In the technique disclosed herein, the form of addition of the colorant (preferably a black colorant such as carbon black particles) to the pressure-sensitive adhesive composition is not particularly limited. A colorant such as carbon black particles can be added to the pressure-sensitive adhesive composition in the form of a dispersion liquid in which the particles are dispersed in a dispersion medium. The dispersion medium constituting the dispersion is not particularly limited, and water (ion exchange water, back-penetration water, distilled water, etc.) and various organic solvents (alcohols such as ethanol; ketones such as acetone; butyl cellosolve, propylene glycol monomethyl) are not particularly limited. Examples include ethers such as ether acetate; esters such as ethyl acetate; aromatic hydrocarbons such as toluene; mixed solvents thereof), and aqueous mixed solvents of water and the above organic solvent. The dispersion liquid may contain the above-mentioned dispersant. By mixing the dispersion with the pressure-sensitive adhesive composition, the pressure-sensitive adhesive composition may contain a colorant (preferably a black colorant such as carbon black particles), and may also contain a dispersant.

The content of the first colorant (preferably a black colorant such as carbon black particles) is appropriately set in consideration of the light-shielding property to be achieved, the dimming property, the required adhesive property, etc., and is specific. Not limited to range. Further, the content of the first colorant may vary depending on the type of pressure-sensitive adhesive, the shape and particle size of the first colorant, compatibility with the pressure-sensitive adhesive, and the like. The content of the first colorant in the pressure-sensitive adhesive layer is preferably about 0.01% by weight or more (for example, 0.05% by weight or more), and is preferably about 0.1% by weight from the viewpoint of light-shielding property. % Or more, more preferably about 0.2% by weight or more, still more preferably about 0.3% by weight or more, particularly preferably about 0.4% by weight or more, even if it is, for example, about 0.5% by weight or more. good. Further, the content of the first colorant (preferably a black colorant such as carbon black particles) can be about 10% by weight or less, about 3% by weight or less is appropriate, and is not more than a predetermined value. From the viewpoint of achieving both a light transmittance and a light reflectance of a predetermined value or more, it is preferably about 2% by weight or less (typically less than 2% by weight), more preferably about 1% by weight or less, and further preferably. It may be about 0.6% by weight or less, about 0.5% by weight or less (for example, 0.4% by weight or less), 0.3% by weight or less, or 0.2% by weight or less. By limiting the content of the first colorant, it tends to be easy to maintain adhesive properties such as adhesive strength.

(Second colorant)
The second colorant contained in the pressure-sensitive adhesive layer is not particularly limited, but is, for example, a component capable of reducing the amount of light entering the pressure-sensitive adhesive layer, and the second colorant is contained in the pressure-sensitive adhesive layer. By doing so, it can be a component that enhances the light reflectance of the pressure-sensitive adhesive layer (hence, also referred to as a “light reflectance improving component”). Such a second colorant can be one or more selected from inorganic materials (eg metals, metal compounds), organic materials, organic-inorganic complexes. Specific examples of the second colorant include titanium oxide (titanium dioxide such as rutyl-type titanium dioxide and anatase-type titanium dioxide), zinc oxide, cerium oxide, aluminum oxide, silicon oxide, zirconium oxide, magnesium oxide, calcium oxide, and oxidation. Metal oxides such as tin, barium oxide, cesium oxide, and ittium oxide; carbonated compounds such as magnesium carbonate, calcium carbonate (light calcium carbonate, heavy calcium carbonate, etc.), barium carbonate, zinc carbonate, etc .; aluminum hydroxide, calcium hydroxide Hydroxides such as magnesium hydroxide and zinc hydroxide; silicate compounds such as aluminum silicate, magnesium silicate and calcium silicate; barium sulfate, calcium sulfate, barium stearate, zinc flower, zinc sulfide, talc, clay, kaolin, phosphoric acid. Inorganic materials such as titanium, mica, gypsum, white carbon, diatomaceous soil, bentonite, lithopon, zeolite, sericite, hydrohalosite, etc., acrylic resin, polystyrene resin, polyurethane resin, amide resin, polycarbonate resin, etc. Examples thereof include organic materials such as silicone-based resins, urea-formalin-based resins, and melamine-based resins. These can be what are referred to as white colorants. The second colorant may be used alone or in combination of two or more. The second colorant does not contain carbon black particles and can be defined as a colorant different from the carbon black particles. Typically, the second colorant does not include a light-absorbing black colorant.

In some preferred embodiments, the pressure-sensitive adhesive layer comprises a metal oxide as a second colorant. By using the first colorant (preferably a black colorant) and the metal oxide in combination, it is possible to preferably achieve both a light transmittance of a predetermined value or less and a light reflectance of a predetermined value or more. As the metal oxide, a material capable of achieving a desired light reflectance can be selected from the above-mentioned materials. Preferable examples include titanium oxide, zinc oxide, cerium oxide, aluminum oxide, silicon oxide, zirconium oxide, magnesium oxide and calcium oxide, among which titanium oxide, silicon oxide and zirconium oxide are preferable, and titanium oxide is particularly preferable. preferable. The metal oxide may be used alone or in combination of two or more.

In the embodiment in which the second colorant has a particle shape, the average particle size of the second colorant (preferably metal oxide particles) is not particularly limited. Depending on the thickness of the pressure-sensitive adhesive layer, the type of pressure-sensitive adhesive, and the like, particles having an appropriate size that can achieve a desired improvement in light reflectance can be used. The average particle size of the second colorant can be, for example, about 1 nm or more, and about 5 nm or more is suitable. From the viewpoint of the effect of containing the second colorant (for example, improvement of light reflectance), compatibility, handleability, etc., the average particle size of the second colorant is preferably about 10 nm or more, and may be about 20 nm or more. , It may be about 30 nm or more. The upper limit of the average particle size is preferably, for example, about 300 nm or less from the viewpoint of maintaining the adhesive properties, and is preferably less than 100 nm (for example, from the viewpoint of improving the light reflectance) containing the second colorant. 90 nm or less), more preferably about 70 nm or less, about 50 nm or less, or about 35 nm or less (for example, about 25 nm or less).

The content of the second colorant (preferably a metal oxide) in the pressure-sensitive adhesive layer is appropriate in consideration of the effect of the second colorant-containing agent (for example, improvement of light reflectance) and the required pressure-sensitive adhesive properties. Is set to, and is not limited to a specific range. Further, the content of the second colorant may differ depending on the type of the pressure-sensitive adhesive, the shape and particle size of the second colorant, compatibility with the pressure-sensitive adhesive, and the like. The content of the second colorant in the pressure-sensitive adhesive layer is preferably about 1% by weight or more, preferably about 2% by weight, from the viewpoint of effectively obtaining the effect of containing the second colorant (for example, improving the light reflectance). % Or more, more preferably about 3% by weight or more, still more preferably about 4% by weight or more, and may be about 5% by weight or more. The content of the second colorant in the pressure-sensitive adhesive layer is approximately 20% by weight or less (for example, less than 20% by weight) from the viewpoint of compatibility with the pressure-sensitive adhesive component and maintenance of pressure-sensitive adhesive properties such as adhesive strength and impact resistance. It is suitable that it is about 10% by weight or less, preferably about 6% by weight or less, and may be about 5% by weight or less.

The ratio of the amount C1 of the first colorant to the amount C2 of the second colorant is appropriately set so as to achieve both the desired light transmittance and the light reflectance, and is not limited to a specific range. In some embodiments, the weight ratio (C1 / C2) of the amount C1 of the first colorant (preferably a black colorant) to the amount C2 of the second colorant (preferably a metal oxide) is 0.001. It may be 0.005 or more, 0.01 or more, 0.05 or more, 0.08 or more, and 0.10 or more (for example, 0.12 or more). The larger the weight ratio (C1 / C2), the more preferably the effect of adding the first colorant is exhibited. In the embodiment in which the first colorant is a black colorant, the light-shielding property of the pressure-sensitive adhesive layer tends to be improved. Further, in some embodiments, the weight ratio (C1 / C2) is 0.50 or less, may be 0.40 or less (for example, 0.35 or less), and is preferably 0.30 or less. It may be 0.20 or less, 0.15 or less, 0.12 or less, 0.09 or less, 0.06 or less (for example, 0.03 or less). The smaller the weight ratio (C1 / C2), the more preferably the effect of adding the second colorant is exhibited. In the embodiment in which the second colorant is a metal oxide, the light reflectance of the pressure-sensitive adhesive layer tends to be improved.

In the embodiment in which the pressure-sensitive adhesive layer contains a black colorant as a first colorant and a metal oxide as a second colorant, the content of the black colorant and the colorant other than the metal oxide is not particularly limited. For example, it can be less than 30% by weight, preferably less than 10% by weight, for example, less than 5.0% by weight, less than 3.0% by weight (for example, less than 2.0% by weight, and even 1). It can be less than% by weight). The technique disclosed herein can be carried out in an embodiment comprising a pressure-sensitive adhesive layer that is substantially free of colorants other than black colorants and metal oxides. In addition, in this specification, "substantially not contained" means that it is not intentionally added, and for example, the content in the pressure-sensitive adhesive layer is 0.3% by weight or less (for example, 0.1% by weight or less, Typically 0.01% by weight or less).

As the colorant, from the viewpoint of compatibility with the pressure-sensitive adhesive component, a material (particulate colorant) exemplified as the above-mentioned colorant, which has been surface-treated with a surface treatment agent, can be used. The surface treatment is not limited to a specific treatment because an appropriate treatment can be selected depending on the type of core particles, the type of dispersion medium, and the like.

The pressure-sensitive adhesive composition disclosed herein may contain a component that contributes to improving the dispersibility of the colorant. The dispersibility-enhancing component may be, for example, a polymer, an oligomer, a liquid resin, a surfactant (anionic, cationic, nonionic, amphoteric surfactant) or the like. As the dispersibility improving component, one kind may be used alone or two or more kinds may be used in combination. The dispersibility improving component is preferably dissolved in the pressure-sensitive adhesive composition. The oligomer is, for example, a low molecular weight polymer of a monomer component containing one or more of the acrylic monomers as exemplified above (for example, Mw is less than about 10 × 10 ⁴ , preferably less than 5 × 10 ⁴ ). Acrylic oligomer). The liquid resin is, for example, a tackifier resin having a softening point of about 50 ° C. or lower, more preferably about 40 ° C. or lower (typically, a tackifier resin such as a rosin-based, terpene-based, or hydrocarbon-based resin, for example, hydrogenated rosin. It can be a methyl ester, etc.). With such a dispersibility improving component, it is possible to suppress uneven dispersion of the colorant (for example, a particulate black colorant such as carbon black), and eventually to suppress color unevenness of the pressure-sensitive adhesive layer. Therefore, it is possible to form a pressure-sensitive adhesive layer having better appearance quality.

The form of addition of the dispersibility improving component is not particularly limited, and may be contained in a liquid containing a colorant (for example, a black colorant such as carbon black particles) before being blended in the pressure-sensitive adhesive composition, or the pressure-sensitive adhesive composition. It may be supplied into the product at the same timing as the colorant or before or after the addition of the colorant.

The content of the dispersibility improving component is not particularly limited, and from the viewpoint of suppressing the influence on the adhesive properties (for example, the decrease in cohesiveness), about 20% by weight or less (preferably about 10% by weight or less) of the entire pressure-sensitive adhesive layer, and more. It is preferably 7% by weight or less, for example, about 5% by weight or less). In some embodiments, the content of the dispersibility improving component can be about 10 times or less (preferably about 5 times or less, for example about 3 times or less) the weight of the colorant. On the other hand, from the viewpoint of preferably exerting the effect of the dispersibility improving component, the content thereof is about 0.2% by weight or more (typically about 0.5% by weight or more, preferably about 1) of the entire pressure-sensitive adhesive layer. Weight% or more) is appropriate. In some embodiments, the content of the dispersibility improving component can be approximately 0.2 times or more (preferably approximately 0.5 times or more, for example 1 time or more) the weight of the colorant.

The content (total amount, total content) of at least two kinds of colorants contained in the pressure-sensitive adhesive layer is compatible with both the desired light transmittance and the light reflectance, and in consideration of the required pressure-sensitive adhesive properties and the like. Properly set and not limited to a specific range. The total amount of the colorant in the pressure-sensitive adhesive layer is preferably about 1% by weight or more, preferably about 2% by weight or more, more preferably about 3% by weight or more, still more preferably about 4% by weight or more, and about 5% by weight. It may be% by weight or more. The total amount of the colorant in the pressure-sensitive adhesive layer can be approximately 30% by weight or less from the viewpoint of compatibility with the pressure-sensitive adhesive component and maintenance of adhesive properties such as adhesive strength and impact resistance, and is approximately 10% by weight. The following is appropriate, preferably about 6% by weight or less, and may be about 5% by weight or less.

(Adhesive-imparting resin)
The pressure-sensitive adhesive layer in the technique disclosed herein may contain a pressure-sensitive adhesive resin. This makes it possible to increase the peel strength of the adhesive sheet. Examples of the pressure-sensitive adhesive resin include phenol-based pressure-sensitive adhesive resin, terpene-based pressure-sensitive adhesive resin, modified terpen-based pressure-sensitive adhesive resin, rosin-based pressure-sensitive adhesive resin, hydrocarbon-based pressure-sensitive adhesive resin, epoxy-based pressure-sensitive adhesive resin, and polyamide-based pressure-sensitive adhesive resin. One or more selected from various known pressure-sensitive adhesives such as an elastomer-based pressure-sensitive adhesive resin and a ketone-based pressure-sensitive adhesive resin can be used. Among them, a phenol-based tackifier resin, a terpene-based tackifier resin, and a modified terpene-based tackifier resin are preferable, and a phenol-based tackifier resin (preferably a terpene phenol resin) is more preferable.

Examples of phenol-based tackifier resins include terpene phenolic resins, hydrogenated terpene phenolic resins, alkylphenolic resins and rosinphenolic resins.
The terpene phenol resin refers to a polymer containing a terpene residue and a phenol residue, and is a copolymer of terpene and a phenol compound (terpene-phenol copolymer resin) and a homopolymer or copolymer of terpene. Is a concept that includes both phenol-modified products (phenol-modified terpene resin). Preferable examples of terpenes constituting such a terpene phenol resin are monoterpenes such as α-pinene, β-pinene, and limonene (including d-form, l-form, and d / l-form (dipentene)). Can be mentioned. The hydrogenated terpene phenol resin refers to a hydrogenated terpene phenol resin having a structure obtained by hydrogenating such a terpene phenol resin. It is also called hydrogenated terpene phenolic resin.
The alkylphenol resin is a resin (oil-based phenol resin) obtained from alkylphenol and formaldehyde. Examples of the alkylphenol resin include novolak type and resol type.
The rosin phenolic resin is typically a phenolic variant of rosins or the various rosin derivatives described above (including rosin esters, unsaturated fatty acid modified rosins and unsaturated fatty acid modified rosin esters). Examples of the rosin phenol resin include a rosin phenol resin obtained by adding phenol to rosins or the above-mentioned various rosin derivatives with an acid catalyst and thermally polymerizing the resin.

Examples of the terpene-based tackifier resin include polymers of terpenes (typically monoterpenes) such as α-pinene, β-pinene, d-limonene, l-limonene, and dipentene. It may be a homopolymer of one kind of terpenes or a copolymer of two or more kinds of terpenes. Examples of the homopolymer of one kind of terpenes include α-pinene polymer, β-pinene polymer, dipentene polymer and the like. Examples of the modified terpene resin include modified terpene resins. Specific examples thereof include styrene-modified terpene resin and hydrogenated terpene resin.

The softening point of the tackifier resin is not particularly limited. From the viewpoint of improving the cohesive force, in some embodiments, a tackifier resin having a softening point (softening temperature) of about 80 ° C. or higher (preferably about 100 ° C. or higher, for example, more than 105 ° C.) can be preferably adopted. In the technique disclosed herein, the total amount of the tackifier resin contained in the pressure-sensitive adhesive layer is 100% by weight, and more than 50% by weight (more preferably more than 70% by weight, for example, more than 90% by weight) has the softening point. It can be preferably carried out in the embodiment of the tackifier resin having. For example, a phenol-based tackifier resin (terpene phenol resin or the like) having such a softening point can be preferably used. The tackifier resin may contain, for example, a terpene phenol resin having a softening point of about 135 ° C. or higher (further, about 140 ° C. or higher). The upper limit of the softening point of the tackifying resin is not particularly limited. From the viewpoint of improving the adhesion to the adherend, in some embodiments, a tackifier resin having a softening point of about 200 ° C. or lower (more preferably about 150 ° C. or lower, for example, less than 130 ° C.) can be preferably used. The softening point of the tackifier resin can be measured based on the softening point test method (ring ball method) specified in JIS K2207.

As some preferred embodiments, the tackifier resin may contain one or more phenolic tackifier resins (typically terpene phenolic resins). The technique disclosed herein can be preferably carried out, for example, in an embodiment in which the total amount of the tackifier resin is 100% by weight, of which about 25% by weight or more (more preferably about 30% by weight or more) is a terpene phenol resin. Approximately 50% by weight or more of the total amount of the tackifier resin may be terpene phenol resin, and approximately 80% by weight or more (for example, approximately 90% by weight or more) may be terpene phenol resin. Substantially all of the tackifier resin (for example, about 95 to 100% by weight, and even about 99 to 100% by weight) may be a terpene phenol resin.

Although not particularly limited, in some embodiments, the tackifier resin may include a tackifier resin having a hydroxyl value higher than 20 mgKOH / g. Of these, a tackifier resin having a hydroxyl value of 30 mgKOH / g or more is preferable. Hereinafter, a tackifier resin having a hydroxyl value of 30 mgKOH / g or more may be referred to as a “high hydroxyl value resin”. According to the tackifier resin containing such a high hydroxyl value resin, a pressure-sensitive adhesive layer having excellent adhesion to an adherend and high cohesive force can be realized. In some embodiments, the tackifier resin may contain a high hydroxyl value resin having a hydroxyl value of 50 mgKOH / g or more (more preferably 70 mgKOH / g or more).
As the value of the hydroxyl value, the value measured by the potentiometric titration method specified in JIS K0070: 1992 can be adopted.

As the high hydroxyl value resin, among the various tackifier resins described above, those having a hydroxyl value of a predetermined value or more can be used. As the high hydroxyl value resin, one type can be used alone or two or more types can be used in combination. For example, as the high hydroxyl value resin, a phenolic tackifier resin having a hydroxyl value of 30 mgKOH / g or more can be preferably adopted. In some preferred embodiments, a terpene phenol resin having a hydroxyl value of at least 30 mgKOH / g is used as the tackifier resin. The terpene phenol resin is convenient because the hydroxyl value can be arbitrarily controlled by the copolymerization ratio of phenol.

The upper limit of the hydroxyl value of the high hydroxyl value resin is not particularly limited. From the viewpoint of compatibility with the base polymer and the like, the hydroxyl value of the high hydroxyl value resin is preferably about 200 mgKOH / g or less, preferably about 180 mgKOH / g or less, more preferably about 160 mgKOH / g or less, still more preferably. It is about 140 mgKOH / g or less. The technique disclosed herein can be preferably carried out in an embodiment in which the tackifier resin contains a high hydroxyl value resin having a hydroxyl value of 30 to 160 mgKOH / g (for example, a phenol-based tackifier resin, preferably a terpene phenol resin). In some embodiments, a high hydroxyl value resin having a hydroxyl value of 30 to 80 mgKOH / g (for example, 30 to 65 mgKOH / g) can be preferably adopted. In some other embodiments, a high hydroxyl value resin having a hydroxyl value of 70 to 140 mgKOH / g may be preferably adopted.

Although not particularly limited, when a high hydroxyl value resin is used, the ratio of the high hydroxyl value resin (for example, terpenephenol resin) to the entire tackifier resin contained in the pressure-sensitive adhesive layer is, for example, about 25% by weight or more. It is preferably about 30% by weight or more, and more preferably about 50% by weight or more (for example, about 80% by weight or more, typically about 90% by weight or more). Substantially all of the tackifier resin (for example, about 95 to 100% by weight, further about 99 to 100% by weight) may be a high hydroxyl value resin.

When the pressure-sensitive adhesive layer contains a pressure-sensitive adhesive resin, the amount of the pressure-sensitive adhesive resin used is not particularly limited, and may be appropriately set in the range of, for example, about 1 to 100 parts by weight with respect to 100 parts by weight of the base polymer. From the viewpoint of preferably exerting the effect of improving the peel strength, it is appropriate that the amount of the tackifier resin used for 100 parts by weight of the base polymer (for example, acrylic polymer) is 5 parts by weight or more, and 10 parts by weight or more. It is preferably 15 parts by weight or more. Further, from the viewpoint of impact resistance and cohesive force, it is appropriate that the amount of the tackifier resin used for 100 parts by weight of the base polymer (for example, acrylic polymer) is 50 parts by weight or less, and even if it is 40 parts by weight or less. It may be 30 parts by weight or less.

(Crosslinking agent)
In the techniques disclosed herein, the pressure-sensitive adhesive composition used to form the pressure-sensitive adhesive layer may contain a cross-linking agent, if necessary. The type of the cross-linking agent is not particularly limited, and a conventionally known cross-linking agent can be appropriately selected and used. Examples of such a cross-linking agent include an isocyanate-based cross-linking agent, an epoxy-based cross-linking agent, an oxazoline-based cross-linking agent, an aziridine-based cross-linking agent, a melamine-based cross-linking agent, a peroxide-based cross-linking agent, a urea-based cross-linking agent, and a metal alkoxide-based cross-linking agent. Examples thereof include a cross-linking agent, a metal chelate-based cross-linking agent, a metal salt-based cross-linking agent, a carbodiimide-based cross-linking agent, a hydrazine-based cross-linking agent, an amine-based cross-linking agent, and a silane coupling agent. Of these, isocyanate-based cross-linking agents, epoxy-based cross-linking agents, oxazoline-based cross-linking agents, aziridine-based cross-linking agents, and melamine-based cross-linking agents are preferable, isocyanate-based cross-linking agents and epoxy-based cross-linking agents are more preferable, and isocyanate-based cross-linking agents are particularly preferable. .. By using an isocyanate-based cross-linking agent, there is a tendency to obtain better impact resistance than other cross-linking systems while obtaining the cohesive force of the pressure-sensitive adhesive layer. Further, the use of an isocyanate-based cross-linking agent is advantageous in terms of improving the adhesive force to an adherend made of a polyester resin such as PET. The cross-linking agent may be used alone or in combination of two or more.

As the isocyanate-based cross-linking agent, polyfunctional isocyanate (meaning a compound having an average of two or more isocyanate groups per molecule, including those having an isocyanurate structure) can be preferably used. The isocyanate-based cross-linking agent may be used alone or in combination of two or more.

Examples of polyfunctional isocyanates include aliphatic polyisocyanates, alicyclic polyisocyanates, aromatic polyisocyanates and the like.
Specific examples of aliphatic polyisocyanes include 1,2-ethylene diisocyanate; 1,2-tetramethylene diisocyanate, 1,3-tetramethylene diisocyanate, 1,4-tetramethylene diisocyanate and other tetramethylene diisocyanates; 1,2. -Hexamethylene diisocyanate such as hexamethylene diisocyanate, 1,3-hexamethylene diisocyanate, 1,4-hexamethylene diisocyanate, 1,5-hexamethylene diisocyanate, 1,6-hexamethylene diisocyanate, 2,5-hexamethylene diisocyanate; Examples thereof include 2-methyl-1,5-pentanediisocyanate, 3-methyl-1,5-pentanediisocyanate and lysine diisocyanate.

Specific examples of the alicyclic polyisocyanates include isophorone diisocyanates; 1,2-cyclohexyldiisocyanates, 1,3-cyclohexyldiisocyanates, 1,4-cyclohexyldiisocyanates and other cyclohexyldiisocyanates; 1,2-cyclopentyldiisocyanates, 1,3. -Cyclopentyl diisocyanate such as cyclopentyl diisocyanate; hydrogenated xylylene diisocyanate, hydrogenated tolylene diisocyanate, hydrogenated diphenylmethane diisocyanate, hydrogenated tetramethylxylylene diisocyanate, 4,4'-dicyclohexylmethane diisocyanate and the like.

Specific examples of aromatic polyisocyanates include 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate, and 2,2'-diphenylmethane diisocyanate. , 4,4'-diphenyl ether diisocyanate, 2-nitrodiphenyl-4,4'-diisocyanate, 2,2'-diphenylpropane-4,4'-diisocyanate, 3,3'-dimethyldiphenylmethane-4,4'-diisocyanate , 4,4'-Diphenylpropane diisocyanate, m-phenylenediisocyanate, p-phenylenediisocyanate, naphthylene-1,4-diisocyanate, naphthylene-1,5-diisocyanate, 3,3'-dimethoxydiphenyl-4,4'-diisocyanate , Xylylene-1,4-diisocyanate, xylylene-1,3-diisocyanate and the like.

Preferred polyfunctional isocyanates are exemplified by polyfunctional isocyanates having an average of 3 or more isocyanate groups per molecule. Such trifunctional or higher functional isocyanates are bifunctional or trifunctional or higher functional isocyanate multimers (typically dimers or trimers), derivatives (eg, polyhydric alcohols and two or more molecules of polyfunctional isocyanates). It can be an addition reaction product), a polymer, or the like. For example, diphenylmethane diisocyanate dimer or trimer, hexamethylene diisocyanate isocyanurate (isocyanurate structure trimer adduct), reaction product of trimethylolpropane and tolylene diisocyanate, trimethylolpropane and hexa. Examples thereof include reaction products with methylene diisocyanate, polyfunctional isocyanates such as polymethylene polyphenyl isocyanate, polyether polyisocyanate, and polyester polyisocyanate. Commercially available products of such polyfunctional isocyanates include the trade name "Duranate TPA-100" manufactured by Asahi Kasei Chemicals, the trade name "Coronate L", the same "Coronate HL", the same "Coronate HK", and the same "Coronate" manufactured by Tosoh Corporation. "HX", "Coronate 2096" and the like can be mentioned.

The amount of the isocyanate-based cross-linking agent used is not particularly limited. For example, it can be approximately 0.5 parts by weight or more with respect to 100 parts by weight of the base polymer. From the viewpoint of achieving both cohesiveness and adhesion and impact resistance, the amount of the isocyanate-based cross-linking agent used with respect to 100 parts by weight of the base polymer can be, for example, 1.0 part by weight or more, and 1.5 parts by weight. The above (typically 2.0 parts by weight or more, for example 2.5 parts by weight or more) may be used. On the other hand, from the viewpoint of improving the adhesion to the adherend, the amount of the isocyanate-based cross-linking agent used is preferably 10 parts by weight or less with respect to 100 parts by weight of the base polymer, and may be 8 parts by weight or less. 5, 5 parts by weight or less (for example, 3 parts by weight or less) may be used.

In some preferred embodiments, the cross-linking agent is a combination of an isocyanate-based cross-linking agent and at least one cross-linking agent having a different type of cross-linking functional group from the isocyanate-based cross-linking agent. According to the technique disclosed herein, a cross-linking agent other than the isocyanate-based cross-linking agent (that is, a cross-linking agent having a different type of cross-linking reactive group from the isocyanate-based cross-linking agent; hereinafter also referred to as "non-isocyanate-based cross-linking agent"). By using it in combination with an isocyanate-based cross-linking agent, excellent cohesive force can be exhibited. The pressure-sensitive adhesive layer in the technique disclosed herein is obtained by using the above-mentioned cross-linking agent in a form after the cross-linking reaction, a form before the cross-linking reaction, a form partially cross-linked, an intermediate or a composite form thereof, or the like. May contain. The cross-linking agent is typically contained in the pressure-sensitive adhesive layer exclusively in the form after the cross-linking reaction.

The type of non-isocyanate-based cross-linking agent that can be used in combination with the isocyanate-based cross-linking agent is not particularly limited, and can be appropriately selected and used from the above-mentioned cross-linking agents. The non-isocyanate cross-linking agent may be used alone or in combination of two or more.

In some preferred embodiments, an epoxy-based cross-linking agent can be adopted as the non-isocyanate-based cross-linking agent. For example, by using an isocyanate-based cross-linking agent and an epoxy-based cross-linking agent in combination, it is easy to achieve both cohesiveness and impact resistance. As the epoxy-based cross-linking agent, a compound having two or more epoxy groups in one molecule can be used without particular limitation. An epoxy-based cross-linking agent having 3 to 5 epoxy groups in one molecule is preferable. The epoxy-based cross-linking agent may be used alone or in combination of two or more.

Although not particularly limited, specific examples of the epoxy-based cross-linking agent include, for example, N, N, N', N'-tetraglycidyl-m-xylenediolamine, 1,3-bis (N, N-diglycidylaminomethyl). ) Cyclohexane, 1,6-hexanediol diglycidyl ether, polyethylene glycol diglycidyl ether, polyglycerol polyglycidyl ether and the like can be mentioned. Commercially available epoxy-based cross-linking agents include Mitsubishi Gas Chemical Company's product name "TETRAD-C" and product name "TETRAD-X", DIC Corporation's product name "Epicron CR-5L", and Nagase Chemtex. The product name "Denacol EX-512", the product name "TEPIC-G" manufactured by Nissan Chemical Industries, Ltd., and the like can be mentioned.

The amount of the epoxy-based cross-linking agent used is not particularly limited. The amount of the epoxy-based cross-linking agent used should be, for example, more than 0 parts by weight and about 1 part by weight or less (typically about 0.001 to 0.5 parts by weight) with respect to 100 parts by weight of the base polymer. Can be done. From the viewpoint of suitably exhibiting the effect of improving the cohesive force, it is appropriate that the amount of the epoxy-based cross-linking agent used is approximately 0.002 parts by weight or more with respect to 100 parts by weight of the base polymer, and is approximately 0.005 parts by weight. More than parts are preferable, and about 0.008 parts by weight or more are more preferable. Further, from the viewpoint of improving the adhesion to the adherend, it is appropriate that the amount of the epoxy-based cross-linking agent used is about 0.2 parts by weight or less with respect to 100 parts by weight of the base polymer, and is about 0.1 weight by weight. The amount is preferably less than about 0.05 parts by weight, more preferably less than about 0.05 parts by weight, still more preferably less than about 0.03 parts by weight (for example, about 0.025 parts by weight or less). Impact resistance tends to be improved by reducing the amount of the epoxy-based cross-linking agent used.

In the technique disclosed herein, the relationship between the content of the isocyanate-based cross-linking agent and the content of the non-isocyanate-based cross-linking agent (for example, an epoxy-based cross-linking agent) is not particularly limited. The content of the non-isocyanate-based cross-linking agent can be, for example, approximately 1/50 or less of the content of the isocyanate-based cross-linking agent. From the viewpoint of more preferably achieving both adhesion to the adherend and cohesive force, the content of the non-isocyanate-based cross-linking agent should be about 1/75 or less of the content of the isocyanate-based cross-linking agent on a weight basis. It is suitable, and is preferably about 1/100 or less (for example, 1/150 or less). Further, from the viewpoint of preferably exerting the effect of using the isocyanate-based cross-linking agent and the non-isocyanate-based cross-linking agent (for example, epoxy-based cross-linking agent) in combination, the content of the non-isocyanate-based cross-linking agent is the same as that of the isocyanate-based cross-linking agent. It is appropriate that the content is about 1/1000 or more, for example, about 1/500 or more.

The total amount (total amount) of the cross-linking agent used is not particularly limited. For example, it can be about 10 parts by weight or less with respect to 100 parts by weight of the base polymer (preferably acrylic polymer), preferably about 0.005 to 10 parts by weight, and more preferably about 0.01 to 5 parts by weight. You can select from the range of parts.

(anti-rust)
The pressure-sensitive adhesive layer according to some preferred embodiments may contain a rust inhibitor. The rust preventive is not particularly limited, and is not particularly limited, and is an azole rust preventive, an amine compound, nitrites, ammonium benzoate, ammonium phthalate, ammonium stearate, ammonium palmitate, ammonium oleate, ammonium carbonate, dicyclohexylamine benzoic acid. Examples thereof include acid salt, urea, urotropin, thiourea, phenylcarbamate, cyclohexylammonium-N-cyclohexylcarbamate (CHC) and the like. The rust preventive may be used alone or in combination of two or more.

As the rust preventive, an azole-based rust preventive can be preferably used. As the azole-based rust preventive agent, a five-membered ring aromatic compound containing two or more heteroatoms, wherein an azole-based compound in which at least one of the heteroatoms is a nitrogen atom is preferably used as an active ingredient. Can be. A preferable example of a compound that can be used as an azole-based rust inhibitor is a benzotriazole-based rust inhibitor containing a benzotriazole-based compound as an active ingredient. Preferable examples of the benzotriazole-based compound include 1,2,3-benzotriazole, 5-methylbenzotriazole, 4-methylbenzotriazole, carboxybenzotriazole and the like.

The content of the rust inhibitor is not particularly limited, and can be, for example, 0.01 part by weight or more (typically 0.05 part by weight or more) with respect to 100 parts by weight of the base polymer. From the viewpoint of obtaining a better metal corrosion prevention effect, the content may be 0.1 parts by weight or more, 0.3 parts by weight or more, or 0.5 parts by weight or more. On the other hand, from the viewpoint of enhancing the cohesive force of the pressure-sensitive adhesive, the content of the rust inhibitor is appropriately less than 8 parts by weight with respect to 100 parts by weight of the base polymer, and may be 5 parts by weight or less, and 2 parts by weight. It may be less than or equal to a part.

(Other additives)
The field of pressure-sensitive adhesives such as leveling agents, cross-linking aids, plasticizers, softeners, antistatic agents, antioxidants, UV absorbers, antioxidants, light stabilizers, etc., as required in the pressure-sensitive adhesive composition. Various additives commonly used in the above may be contained. As for such various additives, conventionally known additives can be used by a conventional method and do not particularly characterize the present invention, and therefore detailed description thereof will be omitted.

(Adhesive composition)
The pressure-sensitive adhesive layer (layer composed of a pressure-sensitive adhesive) disclosed herein is a water-based pressure-sensitive adhesive composition, a solvent-type pressure-sensitive adhesive composition, a hot-melt type pressure-sensitive adhesive composition, and active energy rays such as ultraviolet rays and electron beams. It can be a pressure-sensitive adhesive layer formed from an active energy ray-curable pressure-sensitive adhesive composition that cures by irradiation. The water-based pressure-sensitive adhesive composition refers to a pressure-sensitive adhesive composition in which a pressure-sensitive adhesive (sticking agent layer-forming component) is contained in a solvent containing water as a main component (water-based solvent), and is typically water-dispersed. A type pressure-sensitive adhesive composition (a composition in which at least a part of the pressure-sensitive adhesive is dispersed in water) or the like is included. Further, the solvent-type pressure-sensitive adhesive composition refers to a pressure-sensitive adhesive composition in which the pressure-sensitive adhesive is contained in an organic solvent. As the organic solvent contained in the solvent-type pressure-sensitive adhesive composition, one kind or two or more kinds exemplified as the organic solvent (toluene, ethyl acetate, etc.) that can be used in the above-mentioned solution polymerization can be used without particular limitation. The technique disclosed herein can be preferably carried out in an embodiment including a pressure-sensitive adhesive layer formed from a solvent-type pressure-sensitive adhesive composition from the viewpoint of pressure-sensitive adhesive properties and the like. In the embodiment provided with the solvent-type pressure-sensitive adhesive layer formed from the solvent-type pressure-sensitive adhesive composition, the effect of improving the refractive index by the technique disclosed herein is preferably realized.

From the above, according to the present specification, there is provided a pressure-sensitive adhesive composition containing one or more of the components that may be contained in the pressure-sensitive adhesive layer disclosed herein. By using this pressure-sensitive adhesive composition, it is possible to form a pressure-sensitive adhesive layer having a light transmittance of 30% or less and a light reflectance of 8% or more. The pressure-sensitive adhesive composition contains at least two types of colorants. In addition, a component (typically a base polymer) that may be contained in the above-mentioned pressure-sensitive adhesive layer may be contained. The content (% by weight) of each component that can be contained in the pressure-sensitive adhesive layer can be rephrased as the content (% by weight) based on the solid content (also referred to as the non-volatile content standard) in the pressure-sensitive adhesive composition. Since the details of the other pressure-sensitive adhesive compositions are as described in the pressure-sensitive adhesive layer, repeated description thereof will be omitted.

(Formation of adhesive layer)
The pressure-sensitive adhesive layer disclosed herein can be formed by a conventionally known method. For example, a method of forming a pressure-sensitive adhesive layer by applying a pressure-sensitive adhesive composition to a peelable surface (peeling surface) and drying it can be adopted. For a pressure-sensitive adhesive sheet having a support base material, for example, a method (direct method) of directly applying (typically applying) a pressure-sensitive adhesive composition to the support base material and drying it to form a pressure-sensitive adhesive layer is performed. Can be adopted. Further, a method (transfer method) in which a pressure-sensitive adhesive composition is applied to a peelable surface (peeling surface) and dried to form a pressure-sensitive adhesive layer on the surface, and the pressure-sensitive adhesive layer is transferred to a supporting substrate (transfer method). ) May be adopted. As the peeling surface, for example, the surface of a peeling liner described later can be preferably used. The pressure-sensitive adhesive layer disclosed herein is typically formed continuously, but is not limited to such a form, and may have a regular or random pattern such as a dot shape or a striped shape. It may be a formed pressure-sensitive adhesive layer.

The pressure-sensitive adhesive composition can be applied using a conventionally known coater such as a gravure roll coater, a die coater, or a bar coater. Alternatively, the pressure-sensitive adhesive composition may be applied by impregnation, a curtain coating method, or the like.
From the viewpoint of promoting the crosslinking reaction and improving the production efficiency, it is preferable to dry the pressure-sensitive adhesive composition under heating. The drying temperature can be, for example, about 40 to 150 ° C., preferably about 60 to 130 ° C. After the pressure-sensitive adhesive composition is dried, aging may be further performed for the purpose of adjusting the component transfer in the pressure-sensitive adhesive layer, advancing the cross-linking reaction, alleviating the strain that may exist in the pressure-sensitive adhesive layer, and the like.

The pressure-sensitive adhesive layer disclosed herein may have a single-layer structure or may have a multi-layer structure of two or more layers. From the viewpoint of productivity and the like, the pressure-sensitive adhesive layer preferably has a single-layer structure.

The thickness of the pressure-sensitive adhesive layer is not particularly limited. From the viewpoint of avoiding excessive thickening of the pressure-sensitive adhesive sheet, the thickness of the pressure-sensitive adhesive layer is preferably about 100 μm or less, preferably about 70 μm or less, and more preferably about 50 μm or less. The thickness of the pressure-sensitive adhesive layer can be about 35 μm or less, for example, it may be about 25 μm or less, and further may be about 15 μm or less. The thickness-limited pressure-sensitive adhesive layer can well meet the demand for thinner and lighter weight. The lower limit of the thickness of the pressure-sensitive adhesive layer is not particularly limited, and from the viewpoint of adhesion to the adherend, it is advantageous to set it to about 1 μm or more, and it is appropriate to set it to about 3 μm or more, preferably about 3 μm. It is 10 μm or more, more preferably about 15 μm or more, still more preferably about 20 μm or more, and may be about 30 μm or more, about 35 μm or more, or about 40 μm or more. By setting the thickness to a predetermined value or more, it is possible to preferably realize a light transmittance of a predetermined value or less and a reflectivity of a predetermined value or more. In addition, it is easy to obtain desired adhesive properties (adhesive strength, impact resistance, etc.).

<Supporting base material>
In the embodiment in which the pressure-sensitive adhesive sheet disclosed herein is in the form of a single-sided pressure-sensitive adhesive type or double-sided pressure-sensitive adhesive sheet with a base material, the base material that supports (linees) the pressure-sensitive adhesive layer includes a resin film, paper, cloth, and rubber. Sheets, foam sheets, metal foils, composites thereof and the like can be used. Examples of the resin film include a polyolefin film such as polyethylene (PE), polypropylene (PP), and an ethylene / propylene copolymer; a polyester film such as polyethylene terephthalate (PET); a vinyl chloride resin film; a vinyl acetate resin film; and a polyimide. Resin film; polyamide resin film; fluororesin film; cellophane and the like. Examples of paper include Japanese paper, kraft paper, glassin paper, high-quality paper, synthetic paper, top-coated paper and the like. Examples of the cloth include woven cloths and non-woven fabrics made by spinning various fibrous substances alone or by blending them. Examples of the fibrous material include cotton, sufu, Manila hemp, pulp, rayon, acetate fiber, polyester fiber, polyvinyl alcohol fiber, polyamide fiber, polyolefin fiber and the like. Examples of the rubber sheet include a natural rubber sheet, a butyl rubber sheet and the like. Examples of the foam sheet include a foamed polyurethane sheet, a foamed polychloroprene rubber sheet, and the like. Examples of the metal foil include aluminum foil, copper foil and the like.

The non-woven fabric referred to here is a concept that mainly refers to a non-woven fabric for an adhesive sheet used in the field of adhesive tape and other adhesive sheets, and is typically a non-woven fabric produced by using a general paper machine. (Sometimes called "paper"). Further, the resin film referred to here is typically a non-porous resin sheet, and is a concept that is distinguished from, for example, a non-woven fabric (that is, does not include a non-woven fabric). The resin film may be a non-stretched film, a uniaxially stretched film, or a biaxially stretched film.

As the supporting base material constituting the pressure-sensitive adhesive sheet with a base material, a base film containing a resin film can be preferably used. The base film is typically an independently shape-maintainable (independent) member. The supporting substrate in the techniques disclosed herein may be substantially composed of such a base film. Alternatively, the supporting base material may include an auxiliary layer in addition to the base film. Examples of the auxiliary layer include a colored layer, a reflective layer, an undercoat layer, an antistatic layer, and the like provided on the surface of the base film.

The resin film is a film containing a resin material as a main component (for example, a component contained in the resin film in an amount of more than 50% by weight). Examples of resin films include polyethylene (PE), polypropylene (PP), ethylene / propylene copolymer and other polyolefin resin films; polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyethylene naphthalate (PEN) and the like. Polyethylene resin film; vinyl chloride resin film; vinyl acetate resin film; polyimide resin film; polyamide resin film; fluororesin film; cellophane; and the like. The resin film may be a rubber-based film such as a natural rubber film or a butyl rubber film. Among them, a polyester film is preferable from the viewpoint of handleability and processability, and a PET film is particularly preferable. In the present specification, the "resin film" is typically a non-porous sheet, and is a concept that is distinguished from so-called non-woven fabrics and woven fabrics (in other words, a concept excluding non-woven fabrics and woven fabrics). be.

The supporting base material may have transparency, or may have light-shielding property or dimming property. In some embodiments, the supporting substrate (eg, a resin film) can contain a colorant. This makes it possible to adjust the light transmission (light shielding property) of the supporting base material. Adjusting the light transmittance (for example, vertical light transmittance) of the support base material may be useful for adjusting the light transmittance of the support base material and also the light transmission of the pressure-sensitive adhesive sheet containing the base material.

As the colorant, conventionally known pigments and dyes can be used as well as the colorant that can be contained in the pressure-sensitive adhesive layer. The colorant is not particularly limited, and may be, for example, a colorant such as black, gray, white, red, blue, yellow, green, yellowish green, orange, purple, gold, silver, and pearl.

In some embodiments, a black colorant can be preferably used as the colorant for the supporting substrate, since the light-shielding property (for example, vertical light transmittance) can be efficiently adjusted by a small amount of the colorant. Specific examples of the black colorant include those exemplified as a colorant that can be contained in the pressure-sensitive adhesive layer. In some preferred embodiments, pigments having an average particle size of 10 nm to 500 nm, more preferably 10 nm to 120 nm (eg, particulate black colorants such as carbon black) can be used.

The amount of the colorant used in the supporting base material (for example, a resin film) is not particularly limited, and the amount may be appropriately adjusted so as to impart desired optical characteristics. It is appropriate that the amount of the colorant used is about 0.1 to 30% by weight of the weight of the supporting base material, for example, 0.1 to 25% by weight (typically 0.1 to 20% by weight). Can be.

The supporting base material (for example, resin film) may contain a filler (inorganic filler, organic filler, etc.), a dispersant (surfactant, etc.), an antistatic agent, an antioxidant, an ultraviolet absorber, if necessary. , Antistatic agents, lubricants, plasticizers and other various additives may be blended. The blending ratio of the various additives is about less than 30% by weight (for example, less than 20% by weight, typically less than 10% by weight).

The supporting base material (for example, a resin film) may have a single-layer structure or may have a multi-layer structure of two layers, three layers or more. From the viewpoint of shape stability, the supporting base material preferably has a single-layer structure. In the case of a multi-layer structure, it is preferable that at least one layer (preferably all layers) is a layer having a continuous structure of the above resin (for example, a polyester resin). The method for producing the supporting base material (typically, the resin film) may be appropriately adopted by a conventionally known method, and is not particularly limited. For example, conventionally known general film molding methods such as extrusion molding, inflation molding, T-die casting molding, and calender roll molding can be appropriately adopted.

The supporting base material may be colored by a colored layer arranged on the surface of the base film (preferably a resin film). In the base material having a structure including the base film and the coloring layer as described above, the base film may or may not contain a coloring agent. The colored layer may be arranged on one surface of the base film, or may be arranged on both surfaces, respectively. In the configuration in which the colored layers are arranged on both surfaces of the base film, the configurations of the colored layers may be the same or different.

Such a colored layer can typically be formed by applying a colored layer forming composition containing a colorant and a binder to a base film. As the colorant, conventionally known pigments and dyes can be used as well as the colorant that can be contained in the pressure-sensitive adhesive layer or the resin film. As the binder, a material known in the field of paint or printing can be used without particular limitation. For example, polyurethane, phenol resin, epoxy resin, urea melamine resin, polymethyl methacrylate and the like are exemplified. The composition for forming a colored layer may be, for example, a solvent type, an ultraviolet curable type, a thermosetting type or the like. The colored layer can be formed by using the means conventionally used for forming the colored layer without particular limitation. For example, a method of forming a colored layer (printing layer) by printing such as gravure printing, flexographic printing, and offset printing can be preferably adopted.

The colored layer may have a single-layer structure including one layer as a whole, or may have a multi-layer structure including two layers, three layers or more sub-colored layers. A multi-layered colored layer including two or more sub-colored layers can be formed, for example, by repeatedly applying (for example, printing) a composition for forming a colored layer. The color and the blending amount of the colorant contained in each sub-colored layer may be the same or different. In the colored layer for imparting light-shielding property, it is particularly meaningful to have a multi-layer structure from the viewpoint of preventing the occurrence of pinholes and increasing the reliability of light leakage prevention.

The thickness of the entire colored layer is preferably about 1 μm to 10 μm, preferably about 1 μm to 7 μm, and can be, for example, about 1 μm to 5 μm. In the colored layer including two or more sub-colored layers, the thickness of each sub-colored layer is preferably about 1 μm to 2 μm.

The thickness of the supporting base material is not particularly limited. From the viewpoint of avoiding the pressure-sensitive adhesive sheet from becoming excessively thick, the thickness of the supporting base material can be, for example, about 200 μm or less (for example, about 100 μm or less). Depending on the purpose and mode of use of the pressure-sensitive adhesive sheet, the thickness of the supporting base material may be about 70 μm or less, about 30 μm or less, or about 15 μm or less (for example, about 8 μm or less). The lower limit of the thickness of the supporting base material is not particularly limited. From the viewpoint of handleability (handleability) and processability of the pressure-sensitive adhesive sheet, the thickness of the supporting base material is preferably about 2 μm or more, preferably about 5 μm or more, for example, about 10 μm or more.

The surface of the supporting base material may be subjected to conventionally known surface treatments such as corona discharge treatment, plasma treatment, ultraviolet irradiation treatment, acid treatment, alkali treatment, and application of an undercoat agent. Such a surface treatment may be a treatment for improving the adhesion between the supporting base material and the pressure-sensitive adhesive layer, in other words, the anchoring property of the pressure-sensitive adhesive layer on the supporting base material.

Further, when the technique disclosed herein is carried out in the form of a single-sided pressure-sensitive adhesive sheet with a base material, the back surface of the supporting base material may be subjected to a peeling treatment, if necessary. In the peeling treatment, for example, a general silicone-based, long-chain alkyl-based, fluorine-based or other peeling treatment agent is formed into a thin film of typically 0.01 μm to 1 μm (for example, 0.01 μm to 0.1 μm). It can be a process of giving. By performing such a peeling treatment, it is possible to obtain an effect such as facilitating the rewinding of the wound body in which the adhesive sheet is wound in a roll shape.

<Peeling liner>
In the technique disclosed herein, a release liner can be used in the formation of an adhesive layer, the production of an adhesive sheet, the storage of an adhesive sheet before use, distribution, shape processing, and the like. The release liner is not particularly limited, and is, for example, a release liner having a release treatment layer on the surface of a liner base material such as a resin film or paper, a fluoropolymer (polytetrafluoroethylene or the like), or a polyolefin resin (polyethylene, etc.). A release liner or the like made of a low adhesive material (polypropylene or the like) can be used. The peeling treatment layer may be formed by surface-treating the liner base material with a peeling treatment agent such as a silicone-based, long-chain alkyl-based, fluorine-based, or molybdenum sulfide.

<Characteristics of adhesive sheet, etc.>
(Adhesive force)
The 180-degree peel strength (adhesive strength) of the pressure-sensitive adhesive sheet disclosed herein may vary depending on the purpose of use and the place of application, and is not limited to a specific range. From the viewpoint of obtaining good adhesiveness to the adherend, it is appropriate that the adhesive strength of the pressure-sensitive adhesive sheet is, for example, about 1.0 N / 25 mm or more, preferably about 5.0 N / 25 mm or more, more preferably. Is approximately 10 N / 25 mm or more, and may be approximately 15 N / 25 mm or more. According to the technique disclosed herein, the pressure-sensitive adhesive layer contains at least two kinds of colorants, and realizes the above-mentioned pressure-sensitive adhesive force while having a light transmittance of a predetermined value or less and a light reflectance of a predetermined value or more. Can be done. The upper limit of the adhesive strength is not particularly limited, and may be approximately 30 N / 25 mm or less (for example, 25 N / 25 mm or less). The adhesive strength can be measured by the method described in Examples described later. In the case of a double-sided adhesive sheet having adhesive surfaces on both sides, the adhesive strength on each surface may be the same or different.

(Shear adhesive force)
Although not particularly limited, the pressure-sensitive adhesive sheet disclosed herein preferably exhibits a shear adhesive force of, for example, 1.0 MPa or more. The pressure-sensitive adhesive sheet exhibiting such a shearing adhesive force exhibits strong resistance to a force (that is, a shearing force) that tries to shift the adhesive interface, and thus is excellent in the holding performance of the adherend. From the viewpoint of exhibiting higher holding performance, the shear adhesive force of the pressure-sensitive adhesive sheet is preferably 1.8 MPa or more, more preferably 2.0 MPa or more, still more preferably 2.2 MPa or more. The upper limit of the shear adhesive force is not particularly limited, and generally, the higher the upper limit, the more preferable. On the other hand, from the viewpoint of facilitating the realization of a light transmittance of a predetermined value or less and a light reflectance of a predetermined value or more, in some embodiments, the shear adhesive force may be, for example, 20 MPa or less, or 10 MPa or less. It may be 5 MPa or less, or 3 MPa or less. The shear adhesive force can be measured by the method described in Examples described later.

(Light transmittance)
Although not particularly limited, the pressure-sensitive adhesive sheet preferably has a light transmittance of 30% or less. Such an adhesive sheet may have a light-shielding property suitable for preventing light leakage. Further, it is suitable for concealing the adherend and adjusting the appearance of the adherend through the adhesive sheet (for example, suppressing uneven appearance), and can impart designability. The light transmittance of the pressure-sensitive adhesive sheet is preferably 28% or less , more preferably 25% or less, still more preferably 20% or less, and may be 18% or less, and in some preferred embodiments, the light of the pressure-sensitive adhesive sheet. The transmittance is less than 12%, may be less than 10%, may be less than 8.0%, may be less than 6.0%, may be less than 4.0%, and may be less than 3.0%. The lower the light transmittance, the better the light-shielding property and the hiding property. The lower limit of the light transmittance is not particularly limited, and may be substantially 0%, that is, may be equal to or less than the detection limit, may be 0.05% or more, may be 0.1% or more, and may be 1.0. It may be% or more, 2.0% or more, and 5.0% or more. In some embodiments, the light transmittance of the pressure-sensitive adhesive sheet is 8.0% or more, and may be 12% or more (for example, 15% or more). By having a certain degree of light transmittance, it is possible to appropriately conceal the adherend, adjust the appearance of the adherend (for example, a metal material), and impart a design that retains the texture of the adherend. can. A pressure-sensitive adhesive sheet having moderate light transmission is preferable from the viewpoint of maintaining the pressure-sensitive adhesive properties, productivity, and the like.

The light transmittance of the pressure-sensitive adhesive sheet can be measured by the method described in Examples described later. The light transmittance of the pressure-sensitive adhesive sheet can be adjusted by adjusting the pressure-sensitive adhesive-containing component (for example, the type and amount of the colorant (preferably a black colorant)), the base material-containing component, the thickness of each layer, and the like.

(Light reflectance)
Further, the light reflectance of the pressure-sensitive adhesive sheet is preferably 8.0% or more. In addition to limiting the light transmittance of the pressure-sensitive adhesive layer, the light transmittance on the surface of the pressure-sensitive adhesive sheet is set to 8% or more to reflect light on the pressure-sensitive adhesive surface and reduce the amount of light entering the pressure-sensitive adhesive. It is possible to achieve both light-shielding and dimming properties and high-precision optical control. The light reflectance of the pressure-sensitive adhesive sheet is preferably 9.0% or more, more preferably 10% or more, still more preferably 12% or more, and may be 14% or more (for example, 16% or more). Since the upper limit of the light reflectance is set in an appropriate range in relation to the light transmittance, it is not limited to a specific range, for example, it is less than 40%, may be 30% or less, and may be 20%. It may be less than or equal to (for example, 15% or less).

The light reflectance of the pressure-sensitive adhesive sheet can be measured by the method described in Examples described later. The light reflectance of the pressure-sensitive adhesive sheet can be adjusted by the pressure-sensitive adhesive-containing component (for example, the type and amount of the colorant (preferably a metal oxide) used), the base material-containing component, and the like.

In the case of a double-sided adhesive sheet having adhesive surfaces on both sides, the light reflectance of each surface (each adhesive surface; the first adhesive surface and the second adhesive surface) may be the same or different.

The light transmittance and the light reflectance of the pressure-sensitive adhesive sheet are not particularly limited, and for example, the ratio (R / T) of the light reflectance R to the light transmittance T of the pressure-sensitive adhesive sheet is preferably 0.4 or more. It is preferably 0.5 or more, more preferably 1.0 or more, still more preferably 2.0 or more, and particularly preferably 4.0 or more (for example, 4.5 or more). Further, the upper limit of the ratio (R / T) is about 10 or less, and may be, for example, 5 or less. In the embodiment in which the pressure-sensitive adhesive sheet is required to have a certain degree of light transmission, the ratio (R / T) may be less than 3, may be less than 2, or may be less than 1.

(Total thickness)
The total thickness of the pressure-sensitive adhesive sheet disclosed herein (including the pressure-sensitive adhesive layer and further including the support base material in the configuration having the support base material, but not including the release liner) is not particularly limited. The total thickness of the pressure-sensitive adhesive sheet can be, for example, about 300 μm or less, and from the viewpoint of thinning, about 200 μm or less is appropriate, and it may be about 100 μm or less (for example, about 70 μm or less). In some preferred embodiments, the thickness of the pressure-sensitive adhesive sheet can be approximately 50 μm or less, and may be, for example, approximately 35 μm or less. The lower limit of the thickness of the adhesive sheet is not particularly limited, but can be about 1 μm or more, for example, about 3 μm or more is appropriate, preferably about 6 μm or more, more preferably about 10 μm or more (for example, about 15 μm). Above), more preferably about 20 μm or more. An adhesive sheet having a thickness of a predetermined value or more tends to be easy to handle, and also has excellent adhesiveness and impact resistance. In the base material-less pressure-sensitive adhesive sheet, the thickness of the pressure-sensitive adhesive layer is the total thickness of the pressure-sensitive adhesive sheet.

<Use>
The pressure-sensitive adhesive sheet disclosed herein is suitable for various applications in which light-shielding property and dimming property are required. For example, some electronic devices such as portable electronic devices include light emitting elements for the purpose of displaying images, etc. Therefore, the adhesive sheet has limited light transmission (for example, light shielding property) in order to prevent light leakage and the like. ) Can be required. Further, it may be required to conceal the member or adjust the appearance by using the adhesive sheet. Adhesive sheets disclosed herein are suitable for such electronic devices.

Non-limiting examples of the above-mentioned portable electronic devices include mobile phones, smartphones, tablet computers, laptop computers, various wearable devices (for example, wristwear type worn on the wrist like a wristwatch, clips, straps, etc.). Modular type to be attached to a part of, eyewear type including glasses type (monocular type and binocular type, including head mount type), clothes type to be attached to shirts, socks, hats, etc. in the form of accessories, earphones (Earwear type, etc. attached to the ear), digital camera, digital video camera, audio equipment (portable music player, IC recorder, etc.), computer (computer, etc.), portable game equipment, electronic dictionary, electronic notebook, electronic book, in-vehicle Includes information devices, mobile radios, mobile TVs, mobile printers, mobile scanners, mobile modems, etc. In addition, in this specification, "portable" means that it is not enough to be portable, but to have a level of portability that an individual (standard adult) can carry relatively easily. It shall mean. Examples of the electronic device include a personal computer (desktop type, notebook type, tablet type, etc.), a television, and the like. These may have a built-in display device (display device) such as a liquid crystal display or an organic EL.

The pressure-sensitive adhesive sheet disclosed herein can be used, for example, for the purpose of fixing a pressure-sensitive sensor to another member in a portable electronic device including a pressure-sensitive sensor among such portable electronic devices. In some embodiments, the adhesive sheet is a device for indicating a position on the screen (typically a pen-type or mouse-type device) and a device for detecting the position, and is a plate corresponding to the screen (typically, a pen-type or mouse-type device). Used to fix the pressure sensor to other members in an electronic device (typically a portable electronic device) that has a function that allows the absolute position to be specified on a touch panel). Can be.

Further, the adhesive sheet disclosed herein is suitable for use in a portable electronic device, which is arranged on the back surface of a display screen (display unit) of a touch panel display or the like. By arranging the adhesive sheet disclosed here on the back surface of the display screen (display unit), it is possible to prevent deterioration of the visibility of the display screen regardless of the usage mode of the portable electronic device.

Further, the adhesive sheet disclosed herein is suitable for a portable electronic device having a built-in optical sensor. Various devices such as the above-mentioned portable electronic devices use infrared rays, visible rays, ultraviolet rays, and the like for the purpose of operating the devices, detecting nearby objects, detecting the ambient brightness (ambient light), and data communication. It may be equipped with an optical sensor. Although not particularly limited, examples of the optical sensor include an acceleration sensor, a proximity sensor, a brightness sensor (ambient light sensor), and the like. Such an optical sensor may have a light receiving element for light rays such as ultraviolet rays, visible rays, and infrared rays, and may have a light emitting element for specific light rays such as infrared rays. In other words, the optical sensor may include a light emitting element and / or a light receiving element of a light ray in a specific wavelength region among the wavelength regions including ultraviolet rays, visible rays, and infrared rays. For such devices, the techniques disclosed herein are applied to control the light in the device and activate the sensor by limiting the entry of light that can be refracted and scattered within the pressure-sensitive adhesive layer. It is possible to prevent a decrease in accuracy.

The material (adhesive material) to which the adhesive sheet disclosed herein is attached is not particularly limited, but for example, copper, silver, gold, iron, tin, palladium, aluminum, nickel, titanium, and the like. Metallic materials such as chromium, zinc, or alloys containing two or more of these, for example, polyimide resins, acrylic resins, polyether nitrile resins, polyether sulfone resins, polyester resins (PET resins, polyethylene). Naphthalate resin, etc.), Polyvinyl chloride resin, Polyphenylene sulfide resin, Polyether ether ketone resin, Polyamide resin (so-called aramid resin, etc.), Polyallylate resin, Polycarbonate resin, Liquid crystal polymer, etc. Examples thereof include materials (typically plastic materials), alumina, zirconia, soda glass, quartz glass, inorganic materials such as carbon, and the like. Among them, metal materials such as copper, aluminum and stainless steel, polyester resins such as PET, and resin materials such as polyimide resins, aramid resins and polyphenylene sulfide resins (typically plastic materials) are widely used. ing. The above-mentioned material may be a material of a member constituting a product such as an electronic device. The pressure-sensitive adhesive sheet disclosed herein can be used by being attached to a member made of the above-mentioned material. Further, the above-mentioned material may be a material constituting the above-mentioned fixed object (for example, a back surface member such as an electromagnetic wave shield or a reinforcing plate) such as the pressure-sensitive sensor and the display unit. The fixed object is an object to which the adhesive sheet is attached, that is, an adherend. Further, the back surface member means, for example, a member arranged on the opposite side of the front surface (visual recognition side) of the pressure sensor and the display unit in a portable electronic device, for example, a display device shown in FIG. 3 described later. It may be a member or the like constituting the support portion 240 arranged on the back surface of the 200. Further, the object to be fixed may be in either a single-layer structure or a multi-layer structure, and the surface (pasting surface) on which the pressure-sensitive adhesive sheet is attached may be subjected to various surface treatments. Although not particularly limited, as an example of the object to be fixed, a back surface member having a thickness of 1 μm or more (typically 5 μm or more, for example, 60 μm or more, further 120 μm or more) and 1500 μm or less (for example, 800 μm or less) is used. Can be mentioned.

Further, the member or material to which the pressure-sensitive adhesive sheet is attached (in the case of a double-sided pressure-sensitive adhesive sheet, at least one adherend) may have light transmission. In such a light-transmitting adherend, for example, the light beam of the sensor passes through the adherend and reaches the pressure-sensitive adhesive sheet, so that the effect of the technique disclosed herein (in the pressure-sensitive adhesive layer utilizing light reflectivity). It is easy to obtain the advantages of refraction of light and suppression of scattering. The light transmittance of the adherend may be larger than, for example, 50% and may be 70% or more. In some preferred embodiments, the adherend may have a light transmittance of 80% or higher, more preferably 90% or higher, and 95% or higher (eg, 95-100%). Such a material may be a resin film (for example, a polyester resin film such as a PET film) arranged on the back surface of an image display unit of various devices such as portable electronic devices. The pressure-sensitive adhesive sheet disclosed herein can be preferably used in a mode of being attached to an adherend (for example, a member) having a light transmittance of a predetermined value or more as described above. The light transmittance can be measured by the same method as the light transmittance of the pressure-sensitive adhesive layer.

From the above, according to the technique disclosed herein, a laminate including an adhesive sheet and a member to which the adhesive sheet is attached is provided. In some embodiments, the laminate comprising the pressure-sensitive adhesive sheet is a laminate comprising the pressure-sensitive adhesive sheet and a metal member (first member). Further, in some embodiments, the member to which the pressure-sensitive adhesive sheet is attached may have the light transmittance of the adherend material described above. In this embodiment, the laminated body including the pressure-sensitive adhesive sheet is a laminated body including the pressure-sensitive adhesive sheet and a member having light transmission property (second member). In some preferred embodiments, the laminate is a laminate comprising a metal member (first member), an adhesive sheet, and a light transmissive member (second member) in this order. The pressure-sensitive adhesive sheet is also referred to as a pressure-sensitive adhesive layer in the laminated body.

FIG. 2 shows a configuration example of the laminated body. The laminated body 50 shown in FIG. 2 includes a first member 41, a base material-less adhesive sheet 1, and a second member 42 in this order. Specifically, in the laminated body 50, one adhesive surface (first adhesive surface) 1A of the base material-less adhesive sheet 1 is adhered to the first member 41, and the other adhesive surface of the adhesive sheet 1 (1). Second adhesive surface) 1B is adhered to the second member 42. In this embodiment, both the first member 41 and the second member 42 have a sheet-like or plate-like shape, and the laminated body 50 has a multi-layer structure. Since the details of the members constituting the laminated body have been described as the above-mentioned members, materials, and adherends, the overlapping description will not be repeated.

In some preferred embodiments, the first member 41 is a metal member, the metal material exemplified as the adherend material described above is used. The metal member as the first member 41 is preferably an aluminum member or a stainless steel member, and more preferably a stainless steel member. By attaching the pressure-sensitive adhesive sheet 1 disclosed here to the metal member as the first member 41, the metal member can be well concealed. Such a metal member may be, for example, a member constituting the support portion 240 of the display device 200 shown in FIG. 3 described later. Further, in some preferred embodiments, the second member 42 is a light-transmitting member and has the light transmittance of the above-mentioned light-transmitting adherend. The second member 42 is preferably a member made of a resin film, and more preferably a polyester-based resin film (more specifically, a PET-based resin film). The second member 42 may be, for example, a member arranged on the back surface side of the display unit in the display device. In the embodiment in which the pressure-sensitive adhesive sheet 1 is attached to the light-transmitting member as the second member 42, the light entering through the light-transmitting member can be reflected by the adhesive surface to reduce the amount of light entering the pressure-sensitive adhesive layer. can. The laminate 50 as described above can typically be a component of an organic EL display device, a liquid crystal display device, or the like. The laminate 50 is suitable for use, for example, to be arranged on the back surface of an image display unit (which may be a display unit such as a touch panel display) of various devices such as portable electronic devices.

The pressure-sensitive adhesive sheet disclosed herein has limited light transmission and may be excellent in light-shielding property in a preferred embodiment. Therefore, various light sources such as LEDs (light emitting diodes), self-luminous organic EL, and the like can be used. It is preferably used for electronic devices including light emitting elements of. For example, it can be preferably used for an electronic device (typically a portable electronic device) provided with an organic EL display device or a liquid crystal display device that requires predetermined optical characteristics.

FIG. 3 is an exploded perspective view schematically showing a configuration example of the display device. As shown in FIG. 3, the display device 200 included in the portable electronic device 100 includes a display unit 220 composed of a cover member, an organic EL unit, and the like, and a support unit 240. The display device 200 is configured to further include an adhesive sheet 230. In this configuration example, the adhesive sheet 230 is in the form of a double-sided adhesive sheet (double-sided adhesive sheet) for fixing the members constituting the display portion 220 and the support portion 240. The support portion 240 includes a substrate (a metal plate such as a stainless steel plate or an aluminum plate) and the like. The pressure-sensitive adhesive sheet disclosed herein is preferably used as a component of the display device as described above.

The matters disclosed herein include:
[1] A display device including a display unit including a cover member and an organic EL unit, and a support unit.
An adhesive sheet is joined to the support portion, and an adhesive sheet is bonded to the support portion.
The pressure-sensitive adhesive sheet has a pressure-sensitive adhesive layer containing at least two kinds of colorants.
The pressure-sensitive adhesive layer is a display device having a light transmittance of 30% or less and a light reflectance of 8% or more.
[2] The display device according to the above [1], which has a built-in optical sensor including a light emitting element and / or a light receiving element of a light ray in a specific wavelength region among wavelength regions including ultraviolet rays, visible rays, and infrared rays.
[3] The display device according to the above [1] or [2], wherein the content of the colorant in the pressure-sensitive adhesive layer is 1% by weight or more and 10% by weight or less.
[4] The display device according to any one of [1] to [3] above, wherein the pressure-sensitive adhesive layer contains a black colorant as a first colorant and a metal oxide as a second colorant.
[5] The display device according to the above [4], wherein the content of the metal oxide in the pressure-sensitive adhesive layer is 1% by weight or more and 6% by weight or less.
[6] The display device according to the above [4] or [5], wherein the content of the black colorant in the pressure-sensitive adhesive layer is less than 2% by weight.
[7] The weight ratio (C1 / C2) of the amount C1 of the first colorant and the amount C2 of the second colorant is in the range of 0.01 to 0.30, and the above [4] to [6]. The display device described in any of.
[8] The display device according to any one of [1] to [7] above, wherein the pressure-sensitive adhesive layer is an acrylic pressure-sensitive adhesive layer containing an acrylic polymer as a base polymer.
[9] The display device according to any one of [1] to [8] above, wherein the thickness of the pressure-sensitive adhesive layer is in the range of 10 to 50 μm.
[10] The display device according to any one of [1] to [9] above, which is a base material-less double-sided adhesive pressure-sensitive adhesive sheet composed of the pressure-sensitive adhesive layer.

[11] It has a pressure-sensitive adhesive layer containing at least two kinds of colorants, and has a pressure-sensitive adhesive layer.
The pressure-sensitive adhesive layer is a pressure-sensitive adhesive sheet having a light transmittance of 30% or less and a light reflectance of 8% or more.
[12] The pressure-sensitive adhesive sheet according to the above [11], wherein the content of the colorant in the pressure-sensitive adhesive layer is 1% by weight or more and 10% by weight or less.
[13] The pressure-sensitive adhesive sheet according to the above [11] or [12], wherein the pressure-sensitive adhesive layer contains a black colorant as a first colorant and a metal oxide as a second colorant.
[14] The pressure-sensitive adhesive sheet according to the above [13], wherein the content of the metal oxide in the pressure-sensitive adhesive layer is 1% by weight or more and 6% by weight or less.
[15] The pressure-sensitive adhesive sheet according to the above [13] or [14], wherein the content of the black colorant in the pressure-sensitive adhesive layer is less than 2% by weight.
[16] The weight ratio (C1 / C2) of the amount C1 of the first colorant and the amount C2 of the second colorant is in the range of 0.01 to 0.30, and the above [13] to [15]. Adhesive sheet described in any of.
[17] The pressure-sensitive adhesive sheet according to any one of [11] to [16] above, wherein the pressure-sensitive adhesive layer is an acrylic pressure-sensitive adhesive layer containing an acrylic-based polymer as a base polymer.
[18] The pressure-sensitive adhesive sheet according to any one of [11] to [17] above, wherein the thickness of the pressure-sensitive adhesive layer is in the range of 10 to 50 μm.
[19] The pressure-sensitive adhesive sheet according to any one of [11] to [18] above, which is a base-less double-sided adhesive pressure-sensitive adhesive sheet composed of the pressure-sensitive adhesive layer.
[20] The adhesive sheet according to any one of the above [11] to [19], which is used for joining members in a portable electronic device.

[21] A laminated body including a metal member (first member) and an adhesive sheet.
The pressure-sensitive adhesive sheet has a pressure-sensitive adhesive layer containing at least two kinds of colorants.
The pressure-sensitive adhesive layer is a laminated body having a light transmittance of 30% or less and a light reflectance of 8% or more.
[22] A laminate comprising a light-transmitting member (second member) and an adhesive sheet.
The pressure-sensitive adhesive sheet has a pressure-sensitive adhesive layer containing at least two kinds of colorants.
The pressure-sensitive adhesive layer is a laminated body having a light transmittance of 30% or less and a light reflectance of 8% or more.
[23] A laminated body including a metal member (first member), an adhesive sheet, and a member having light transmission (second member) in this order.
The pressure-sensitive adhesive sheet has a pressure-sensitive adhesive layer containing at least two kinds of colorants.
The pressure-sensitive adhesive layer is a laminated body having a light transmittance of 30% or less and a light reflectance of 8% or more.
[24] The laminate according to the above [21] or [23], wherein the metal member is an aluminum member or a stainless steel member.
[25] The laminate according to the above [22] or [23], wherein the light transmittance of the member having light transmittance is larger than 50%.
[26] The laminate according to the above [22], [23] or [25], wherein the light-transmitting member is made of a resin film.
[27] The laminate according to any one of [21] to [26] above, wherein the content of the colorant in the pressure-sensitive adhesive layer is 1% by weight or more and 10% by weight or less.
[28] The laminate according to any one of [21] to [27] above, wherein the pressure-sensitive adhesive layer contains a black colorant as a first colorant and a metal oxide as a second colorant.
[29] The laminate according to the above [28], wherein the content of the metal oxide in the pressure-sensitive adhesive layer is 1% by weight or more and 6% by weight or less.
[30] The laminate according to the above [28] or [29], wherein the content of the black colorant in the pressure-sensitive adhesive layer is less than 2% by weight.
[31] The weight ratio (C1 / C2) of the amount C1 of the first colorant and the amount C2 of the second colorant is in the range of 0.01 to 0.30, [28] to [30]. The laminate described in any of.
[32] The laminate according to any one of [21] to [31] above, wherein the pressure-sensitive adhesive layer is an acrylic pressure-sensitive adhesive layer containing an acrylic polymer as a base polymer.
[33] The laminate according to any one of [21] to [32] above, wherein the thickness of the pressure-sensitive adhesive layer is in the range of 10 to 50 μm.
[34] The laminate according to any one of [21] to [33] above, which is a base material-less double-sided adhesive pressure-sensitive adhesive sheet composed of the pressure-sensitive adhesive layer.
[35] The laminate according to any one of the above [21] to [34], which is used for a portable electronic device.

[36] A pressure-sensitive adhesive composition containing at least two kinds of colorants.
[37] The pressure-sensitive adhesive composition according to the above [36], wherein the content of the colorant in the pressure-sensitive adhesive composition is 1% by weight or more and 10% by weight or less based on the solid content.
[38] The pressure-sensitive adhesive composition according to the above [36] or [37], wherein the pressure-sensitive adhesive composition contains a black colorant as a first colorant and a metal oxide as a second colorant.
[39] The pressure-sensitive adhesive composition according to the above [38], wherein the content of the metal oxide in the pressure-sensitive adhesive composition is 1% by weight or more and 6% by weight or less based on the solid content.
[40] The pressure-sensitive adhesive composition according to the above [38] or [39], wherein the content of the black colorant in the pressure-sensitive adhesive composition is less than 2% by weight based on the solid content.
[41] The weight ratio (C1 / C2) of the amount C1 of the first colorant and the amount C2 of the second colorant is in the range of 0.01 to 0.30, and the above [38] to [40]. The pressure-sensitive adhesive composition according to any one of.
[42] The pressure-sensitive adhesive composition according to any one of [36] to [41] above, wherein the pressure-sensitive adhesive composition contains an acrylic polymer as a base polymer.
[43] The pressure-sensitive adhesive according to any one of [36] to [42] above, which is used to form a pressure-sensitive adhesive layer having a light transmittance of 30% or less and a light reflectance of 8% or more. Composition.

Hereinafter, some examples of the present invention will be described, but the present invention is not intended to be limited to those shown in such examples. The "part" in the following description is based on weight unless otherwise specified.

<Evaluation method>
[Light transmittance]
The light transmittance [%] of the pressure-sensitive adhesive layer and the pressure-sensitive adhesive sheet is the light transmittance (light transmittance at a wavelength of 550 nm) in the thickness direction of the pressure-sensitive adhesive layer and the pressure-sensitive adhesive sheet peeled off from the release liner, respectively, and is JIS K 7136. : Measured using a commercially available transmittance meter according to 2000. As the transmittance meter, a spectrophotometer manufactured by Hitachi, Ltd. (device name "U4150 type spectrophotometer") or an equivalent product thereof is used.

[Light reflectance]
The light reflectance (%) on the surface of the pressure-sensitive adhesive layer and the surface of the pressure-sensitive adhesive sheet is determined by using a commercially available spectrophotometer to remove light having a wavelength of 550 nm from the release liner on one surface of the pressure-sensitive adhesive layer or the pressure-sensitive adhesive sheet (light). It is obtained by irradiating the surface of the reflectance measurement surface) and measuring the intensity of the light reflected on the surface irradiated with the light. As the spectrophotometer, for example, a spectrophotometer manufactured by Hitachi, Ltd. (device name "U4150 type spectrophotometer") can be used.

[180 degree peel strength (adhesive strength)]
In a measurement environment of 23 ° C. and 50% RH, a PET film with a thickness of 50 μm is attached to one of the adhesive surfaces of the double-sided adhesive sheet, lined, and cut into a size of 25 mm in width and 100 mm in length to prepare a measurement sample. do. For the prepared measurement sample, the adhesive surface of the measurement sample is pressure-bonded to the surface of the stainless steel plate (SUS304BA plate) by reciprocating a 2 kg roller once in an environment of 23 ° C. and 50% RH. After leaving this in the same environment for 30 minutes, using a universal tensile compression tester, the peel strength (adhesive strength) under the conditions of a tensile speed of 300 mm / min and a peeling angle of 180 degrees according to JIS Z 0237: 2000. ) Measure [N / 25 mm]. As the universal tensile compression tester, for example, a "tensile compression tester, TG-1kN" manufactured by Minebea, or an equivalent product thereof is used. In the case of a single-sided adhesive sheet, the PET film does not need to be lined.

[Shear adhesive force]
An adhesive sheet (double-sided adhesive sheet) is cut into a size of 10 mm × 10 mm to prepare a measurement sample. In an environment of 23 ° C. and 50% RH, each adhesive surface of the above measurement sample is superposed on the surface of two stainless steel plates (SUS304BA plate), and a 2 kg roller is reciprocated once for pressure bonding. After leaving this in the same environment for 2 days, the shear adhesive force [MPa] is measured using a tensile tester under the conditions of a tensile speed of 10 mm / min and a peeling angle of 0 degrees. In the case of a single-sided adhesive sheet (single-sided adhesive sheet), the non-adhesive surface of the sheet may be fixed to a stainless steel plate with an adhesive or the like, and the other may be measured in the same manner as described above. As the tensile tester, a universal tensile compression tester (product name "TG-1kN", manufactured by Minebea) can be used.

<Example 1>
(Preparation of acrylic polymer)
In a reaction vessel equipped with a stirrer, a thermometer, a nitrogen gas introduction tube, a reflux cooler and a dropping funnel, 95 parts of n-butyl acrylate (BA) and 5 parts of acrylic acid (AA) as monomer components were used as a polymerization solvent. 233 parts of ethyl acetate was charged, and the mixture was stirred for 2 hours while introducing nitrogen gas. After removing oxygen in the polymerization system in this way, 0.2 parts of 2,2'-azobisisobutyronitrile (AIBN) was added as a polymerization initiator, and solution polymerization was carried out at 60 ° C. for 8 hours to carry out acrylic. A solution of the system polymer A was obtained. The Mw of this acrylic polymer A was about 70 × ¹⁰⁴ .

(Preparation of adhesive composition)
In the acrylic polymer solution, with respect to 100 parts of the acrylic polymer A contained in the solution, 20 parts of a terpenephenol resin as a tackifier resin, 3 parts of an isocyanate-based cross-linking agent as a cross-linking agent, and 0.01 part of an epoxy-based cross-linking agent. And 0.07% of carbon black particles (manufactured by Dainichi Seika Kogyo Co., Ltd., trade name "ATDN101 Black", average particle size 350 nm) as the first colorant (black colorant) in the pressure-sensitive adhesive layer. Titanium oxide (TiO ₂ ) particles (product name "WHITE PASSE R-2228", manufactured by Dainichi Seika Kogyo Co., Ltd., average particle size 50 nm) as a second colorant (metal oxide) were placed in the pressure-sensitive adhesive layer at 5.10. Was added, and the mixture was stirred and mixed to prepare a pressure-sensitive adhesive composition. As the terpene phenol resin (adhesive-imparting resin), the trade name "YS Polystar T-115" (manufactured by Yasuhara Chemical Co., Ltd., softening point of about 115 ° C., hydroxyl value of 30 to 60 mgKOH / g) was used. As the isocyanate-based cross-linking agent, trade name "Coronate L" (75% ethyl acetate solution of trimethylolpropane / tolylene diisocyanate trimeric adduct manufactured by Tosoh Corporation) was used. As the epoxy-based cross-linking agent, the trade name “TETRAD-C” (manufactured by Mitsubishi Gas Chemical Company, 1,3-bis (N, N-diglycidylaminomethyl) cyclohexane) was used.

(Making an adhesive sheet)
The above pressure-sensitive adhesive composition is applied to the peel-off surface of a 38 μm-thick polyester peel-off liner (trade name “Diafoil MRF”, manufactured by Mitsubishi Polyester), dried at 100 ° C. for 2 minutes, and a 35 μm-thick pressure-sensitive adhesive. Formed a layer. A peeling surface of a polyester peeling liner (trade name "Diafoil MRF", manufactured by Mitsubishi Polyester Co., Ltd.) having a thickness of 25 μm was bonded to this pressure-sensitive adhesive layer. In this way, a base material-less double-sided adhesive sheet having a thickness of 35 μm was obtained, in which both sides were protected by the above two polyester release liners.

<Examples 2-4>
The content of carbon black particles in the pressure-sensitive adhesive layer was changed to 0.15% (Example 2), 0.57% (Example 3), and 0.30% (Example 4), and the content of titanium oxide particles was changed to 4. The pressure-sensitive adhesive composition according to each example was prepared in the same manner as in Example 1 except that the content was changed to .54% (Example 2), 4.48% (Example 3), and 2.33% (Example 4). Using the pressure-sensitive adhesive composition, a substrate-less double-sided pressure-sensitive adhesive sheet according to each example was produced.

<Example 5>
Acrylic polymer B was synthesized in the same manner as in the synthesis of acrylic polymer A except that the monomer composition was changed to 95 parts of 2-ethylhexyl acrylate (2EHA) and 5 parts of AA to obtain a solution of acrylic polymer B. In this acrylic polymer solution, with respect to 100 parts of the acrylic polymer B contained in the solution, 20 parts of a terpene phenol resin, 10 parts of an acrylic oligomer, 3 parts of an isocyanate-based cross-linking agent and an epoxy as a cross-linking agent are used. 0.03 part of the system cross-linking agent was added, and 0.29% of carbon black particles as the first colorant (black colorant) were added to the pressure-sensitive adhesive layer, and titanium oxide particles as the second colorant were added to the pressure-sensitive adhesive layer. A pressure-sensitive adhesive composition was prepared by adding the mixture to 3.65% and stirring and mixing. As the terpenphenol resin, the isocyanate-based cross-linking agent, the epoxy-based cross-linking agent, the carbon black particles, and the titanium oxide particles, those of the same type as those used in Example 1 were used.
As the acrylic oligomer, one prepared by the following method was used. Specifically, in a reaction vessel equipped with a stirrer, a thermometer, a nitrogen gas introduction tube, a reflux cooler, and a dropping funnel, 95 parts of cyclohexyl methacrylate (CHMA) and 5 parts of AA, and 10 parts of AIBN as a polymerization initiator. After adding toluene as a polymerization solvent and stirring in a nitrogen stream for 1 hour to remove oxygen in the polymerization system, the temperature is raised to 85 ° C. and the reaction is carried out for 5 hours to obtain an acrylic oligomer having a solid content concentration of 50%. Obtained. The Mw of the obtained acrylic oligomer was 3600.
A substrateless double-sided pressure-sensitive adhesive sheet having a thickness of 35 μm was obtained in the same manner as in Example 1 except that the obtained pressure-sensitive adhesive composition was used, and both sides were protected by the above two polyester release liners.

<Examples 6 to 7>
The content of carbon black particles in the pressure-sensitive adhesive layer was changed to 0.31% (Example 6) and 0.40% (Example 7), and the content of titanium oxide particles was changed to 5.10% (Example 6), 4 A pressure-sensitive adhesive composition according to each example was prepared in the same manner as in Example 5 except that it was changed to .13% (Example 7), and a substrate-less double-sided pressure-sensitive adhesive sheet according to each example was used using the pressure-sensitive adhesive composition. Was produced.

<Examples 8-9>
The content of carbon black particles in the pressure-sensitive adhesive layer was changed to 0.43% (Example 8) and 0.88% (Example 9), and the content of titanium oxide particles was changed to 4.65% (Example 8), 2 The pressure-sensitive adhesive composition according to each example was prepared in the same manner as in Example 1 except that it was changed to .29% (Example 9), and the base-less double-sided pressure-sensitive adhesive sheet according to each example was used using the pressure-sensitive adhesive composition. Was produced.

<Examples 10 to 11>
The content of the carbon black particles in the pressure-sensitive adhesive layer was changed to 2.00% (Example 10) and 1.34% (Example 11) without using titanium oxide particles, and so on, in the same manner as in Example 1, respectively. The pressure-sensitive adhesive compositions according to the examples were prepared respectively, and the base-less double-sided pressure-sensitive adhesive sheets according to the examples were prepared using the pressure-sensitive adhesive compositions.

Table 1 shows an outline of the pressure-sensitive adhesive according to each example and evaluation results of light transmittance, light reflectance, adhesive strength and shear adhesive strength.

Although specific examples of the present invention have been described in detail above, these are merely examples and do not limit the scope of claims. The techniques described in the claims include various modifications and modifications of the specific examples exemplified above.

1 Adhesive sheet 1A Adhesive surface, 1st adhesive surface 1B Adhesive surface, 2nd adhesive surface 21 Adhesive layer 21A Adhesive surface, 1st adhesive surface 21B Adhesive surface, 2nd adhesive surface 31,32 Peeling liner

Claims (5)

An adhesive composition used for joining members of portable electronic devices.
The pressure-sensitive adhesive composition is a solvent-type pressure-sensitive adhesive composition, a hot-melt type pressure-sensitive adhesive composition, or an active energy ray-curable pressure-sensitive adhesive composition.
The pressure-sensitive adhesive composition contains an acrylic polymer as a base polymer and at least two kinds of colorants.
The colorant contains a black colorant as a first colorant and a light reflectance improving component as a second colorant .
The content of the black colorant is 0.6% by weight or less based on the solid content.
The weight ratio (C1 / C2) of the amount C1 of the first colorant and the amount C2 of the second colorant is 0.001 or more and 0.50 or less.
A pressure-sensitive adhesive composition containing 1 to 20 parts by weight of a tackifier resin having a softening point of 80 ° C. or higher with respect to 100 parts by weight of the base polymer. The pressure-sensitive adhesive composition according to claim 1, wherein the content of the colorant is 1% by weight or more and 10% by weight or less based on the solid content. The pressure-sensitive adhesive composition according to claim 1 or 2, wherein the colorant contains a metal oxide as the second colorant. The pressure-sensitive adhesive composition according to claim 3, wherein the content of the metal oxide is 1% by weight or more and 6% by weight or less based on the solid content. The pressure-sensitive adhesive composition according to any one of claims 1 to 4, wherein the weight ratio (C1 / C2) is in the range of 0.01 to 0.30.

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