JP7058995B2 - Adhesives for repetitive bending devices, adhesive sheets, repetitive bending laminated members and repetitive bending devices - Google Patents

Description

The present invention relates to adhesives and pressure-sensitive adhesives for devices that are repeatedly bent, as well as repeatedly bent laminated members and repeatedly bent devices.

In recent years, a bendable display has been proposed as a display body (display) of an electronic device, which is a kind of device. Such a flexible display is expected to have a wide range of uses, for example, for a stationary display that is curved and installed on a columnar pillar, or for a mobile display that can be bent or rolled and carried.

Examples of the type of the flexible display include an organic electroluminescence (organic EL) display, an electrophoretic display (electronic paper), and a liquid crystal display using a plastic film as a substrate.

In a flexible display as described above, it is common that one flexible member (flexible member) constituting the flexible display and another flexible member are bonded to each other by an adhesive layer of an adhesive sheet. It is considered to be the target. Here, as a conventional non-bendable adhesive sheet for a display, for example, those shown in Patent Documents 1 and 2 are known.

The flexible display may be repeatedly bent (bent) as described in Patent Document 3, instead of being curved only once. Further, in such a repeatedly flexible display, it may be fixed in a bent state for a long period of time. When a conventional adhesive sheet is used for a repetitive flexible display for such applications, the adhesive layer is deformed and the flexible display remains largely bent even after being released from the bent state, and solidifies in the bent state. There was a case that it ended up. In addition, in the bent state, peeling often occurred at the interface between the pressure-sensitive adhesive layer and the adherend at the bent portion.

Japanese Unexamined Patent Publication No. 2015-174907 Japanese Unexamined Patent Publication No. 2016-774 Japanese Unexamined Patent Publication No. 2016-2764

The present invention has been made in view of the above-mentioned actual conditions, and when it is repeatedly bent by being applied to a repeatedly bending device and when it is left in a bending state for a long period of time, it is adhered after being released from the bending state. It is possible to suppress the deformation of the agent layer, alleviate the influence of repeated bending of the repeatedly bending device and the influence of being placed in the bending state, and at the same time, the interface between the adhesive layer and the adherend generated at the bending site. Adhesives and adhesive sheets for repetitive bending devices that can suppress peeling, and the effects of repeated bending and the bending state after being released from the bending state when repeatedly bending and being placed in the bending state for a long period of time. Provided are a repetitive bending laminated member and a repetitive bending device capable of alleviating the influence of being placed on the surface and suppressing peeling of the interface between the pressure-sensitive adhesive layer and the adherend generated at the bending site. The purpose is.

In order to achieve the above object, first, the present invention is a pressure-sensitive adhesive for a repetitive bending device for adhering one flexible member constituting a device to be repeatedly bent to another flexible member. , JIS K7424-1, the maximum relaxation elastic modulus value measured when the pressure-sensitive adhesive is distorted by 10% is set to the maximum relaxation elastic modulus G (t) max (MPa), and the maximum relaxation elastic modulus is defined as the maximum relaxation elastic modulus. The pressure-sensitive adhesive is continuously distorted by 10% until 3757 seconds after the rate G (t) max is measured, and the minimum relaxed modulus value measured during that period is set to the minimum relaxed modulus G (t) min (MPa). The relaxation elastic modulus fluctuation value Δlog G (t) calculated from the following equation (I) is 0.85 or less, and the loss positive contact at 25 ° C. obtained from the dynamic elastic modulus measurement based on JIS K7424-1. (Invention 1) provides a pressure-sensitive adhesive for a repetitive bending device, characterized in that (tan δ) is 0.328 or more and 0.85 or less.
ΔlogG (t) = logG (t) _max -logG (t) _min ... (I)

In the above invention (Invention 1), by satisfying the above physical properties, the pressure-sensitive adhesive layer is released from the bent state when it is repeatedly bent by being applied to a repeatedly bent device and when it is left in the bent state for a long period of time. It is difficult for the device to be deformed, and it is possible to suppress the repeated bending device from solidifying in a greatly bent state, thereby alleviating the influence of the repeated bending of the repeatedly bending device and the influence of being placed in the bending state. Further, in the above invention (Invention 1), by satisfying the above physical properties, high adhesive force is easily exhibited, and even when it is applied to a repeatedly bending device and repeatedly bent or left in a bent state for a long period of time. By the interaction with the fact that the pressure-sensitive adhesive layer is unlikely to be deformed as described above, it is possible to suppress the peeling of the interface between the pressure-sensitive adhesive layer and the adherend that occurs at the bending portion.

In the above invention (Invention 1), the storage elastic modulus (G') at 25 ° C. is preferably 0.01 MPa or more and 0.25 MPa or less (Invention 2).

In the above inventions (Inventions 1 and 2), the loss elastic modulus (G ″) at 25 ° C. is preferably 0.005 MPa or more and 0.1 MPa or less (Invention 3).

In the above inventions (Inventions 1 to 3), the pressure-sensitive adhesive is a pressure-sensitive adhesive obtained by cross-linking a pressure-sensitive adhesive composition containing a (meth) acrylic acid ester polymer (A) and a cross-linking agent (B). It is preferable that there is (Invention 4).

Secondly, the present invention is a pressure-sensitive adhesive sheet having an pressure-sensitive adhesive layer for adhering one flexible member constituting a device to be repeatedly bent and another flexible member, and the pressure-sensitive adhesive layer is a pressure-sensitive adhesive layer. Provided is a pressure-sensitive adhesive sheet comprising the pressure-sensitive adhesives for repeatedly bending devices (Inventions 1 to 4) (Invention 5).

In the above invention (Invention 5), the pressure-sensitive adhesive sheet includes two release sheets, and the pressure-sensitive adhesive layer is sandwiched between the release sheets so as to be in contact with the release surfaces of the two release sheets. (Invention 6).

Thirdly, the present invention has an adhesive layer for bonding one flexible member and another flexible member constituting a device to be repeatedly bent, and the one flexible member and the other flexible member to each other. Provided is a repeatedly bent laminated member comprising the above, wherein the pressure-sensitive adhesive layer is the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet (Invention 5 and 6) (Invention 7).

In the above invention (Invention 7), it is preferable that at least one of the one flexible member and the other flexible member is a display element (Invention 8).

Fourth, the present invention provides a repetitive bending device including the repetitive bending laminated member (inventions 7 and 8) (invention 9).

The pressure-sensitive adhesive and the pressure-sensitive adhesive sheet for a repeatedly bending device according to the present invention can be applied to a repeatedly bending device and repeatedly bent or left in a bent state for a long period of time. Deformation is unlikely to occur, the effect of repeated bending of the repeatedly bending device and the effect of being placed in the bending state can be mitigated, and the peeling of the interface between the adhesive layer and the adherend that occurs at the bending site can be prevented. It can be suppressed. Further, the repeatedly bent laminated member and the repeatedly bent device according to the present invention are subjected to the influence of repeated bending and the bent state after being released from the bent state when repeatedly bent and placed in the bent state for a long period of time. It is possible to mitigate the influence of this, and it is possible to suppress the peeling of the interface between the pressure-sensitive adhesive layer and the adherend generated at the bent portion.

It is sectional drawing of the adhesive sheet which concerns on one Embodiment of this invention. It is sectional drawing of the repeated bending laminated member which concerns on one Embodiment of this invention. It is explanatory drawing (side view) explaining the static bending test. It is explanatory drawing (side view) explaining the amount of deformation of a test piece as a test result of a bending test. It is explanatory drawing (side view) explaining the dynamic bending test.

Hereinafter, embodiments of the present invention will be described.
[Adhesive for repeated bending devices]
The adhesive for a repetitive bending device according to the present embodiment (hereinafter, may be simply referred to as “adhesive”) is for bonding one flexible member constituting the repetitive bending device to another flexible member. Adhesive. The repetitive bending device and the flexible member will be described later.

The pressure-sensitive adhesive according to the present embodiment has a maximum relaxation elastic modulus G (t) max ( MPa), the adhesive is continuously distorted by 10% until 3757 seconds after the maximum relaxation elastic modulus G (t) max is measured, and the minimum relaxation elastic modulus value measured during that period is the minimum relaxation elastic modulus. G (t) min (MPa), the relaxed elastic modulus fluctuation value ΔlogG (t) calculated from the following formula (I) is 0.85 or less, and the dynamic elastic modulus is measured according to JIS K7424-1. The loss tangent (tan δ) at 25 ° C. obtained from the above is 0.328 or more and 0.85 or less.
ΔlogG (t) = logG (t) _max -logG (t) _min ... (I)
The details of the method for measuring the relaxed elastic modulus G (t) and the loss tangent (tan δ) are as shown in the test examples described later.

The pressure-sensitive adhesive according to the present embodiment has a particularly small relaxation elastic modulus fluctuation value as described above, so that the property toward a completely elastic body becomes large, and the stress fluctuation when distorted by a predetermined amount is small, that is, the original. The force to return to is easily maintained. Therefore, the deformation is likely to be restored when the load is removed. Therefore, the pressure-sensitive adhesive layer made of the pressure-sensitive adhesive is adhered even after being released from the bent state when the repeatedly bent device to which the pressure-sensitive adhesive layer is applied is repeatedly bent or left in the bent state for a long period of time. Deformation of the agent layer is unlikely to occur, it is possible to suppress the repeated bending device from solidifying in a greatly bent state, and thus it is possible to mitigate the influence of the repeated bending of the repeated bending device and the influence of being placed in the bent state. This effect may be hereinafter referred to as "the bending state relaxation effect of the repeatedly bending device". As an index of the number of times of repeated bending, 30,000 times is exemplified.

Further, the pressure-sensitive adhesive according to the present embodiment has a particularly large loss tangent (tan δ) as described above, so that the viscosity becomes strong and a high pressure-sensitive adhesive force is easily exhibited. Therefore, even when the repeatedly bent device to which the pressure-sensitive adhesive layer made of the pressure-sensitive adhesive is repeatedly bent or left in a bent state for a long period of time, the relaxation elastic modulus fluctuation value is small as described above, and the adhesive is adhered. The interaction with the fact that the agent layer is unlikely to be deformed suppresses the occurrence of peeling at the interface between the pressure-sensitive adhesive layer and the adherend at the bent portion. This effect may be hereinafter referred to as "interface peeling suppressing effect".

From the viewpoint of the bending state relaxing effect and the interface peeling suppressing effect of the repetitive bending device, the relaxation elastic modulus fluctuation value ΔlogG (t) needs to be 0.85 or less, preferably 0.82 or less. In particular, it is preferably 0.75 or less, and more preferably 0.50 or less. The lower limit of the relaxation elastic modulus fluctuation value is not particularly limited, but is usually preferably 0.10 or more, and particularly preferably 0.15 or more.

The maximum relaxed elastic modulus G (t) _max of the pressure-sensitive adhesive according to the present embodiment is preferably 1.0 MPa or less, particularly preferably 0.95 MPa or less, and further 0.9 MPa or less as an upper limit value. Is preferable. Since the upper limit value of the maximum relaxed elastic modulus G (t) _max is the above, the relaxed elastic modulus fluctuation value Δlog G (t) can easily satisfy the above-mentioned value. The lower limit of the maximum relaxed elastic modulus G (t) _max is not particularly limited, but is usually preferably 0.05 MPa or more, particularly preferably 0.10 MPa or more, and further preferably 0.15 MPa or more. Is preferable.

Further, the minimum relaxed elastic modulus G (t) _min of the pressure-sensitive adhesive according to the present embodiment is preferably 0.005 MPa or more, particularly preferably 0.01 MPa or more, and further 0. It is preferably 02 MPa or more. Since the lower limit value of the minimum relaxed elastic modulus G (t) _min is the above, the relaxed elastic modulus fluctuation value Δlog G (t) can easily satisfy the above-mentioned value. The upper limit of the minimum relaxed elastic modulus G (t) _min is not particularly limited, but is usually preferably 0.50 MPa or less, particularly preferably 0.45 MPa or less, and further preferably 0.40 MPa or less. Is preferable.

On the other hand, the loss tangent (tan δ) of the pressure-sensitive adhesive according to the present embodiment at 25 ° C. is preferably 0.328 or more, particularly 0.45 or more, as a lower limit value from the viewpoint of the interface peeling suppressing effect. It is preferably 0.55, and more preferably 0.55. Further, from the viewpoint of maintaining the shape of the pressure-sensitive adhesive layer, the upper limit of the loss tangent (tan δ) is preferably 0.85 or less, particularly preferably 0.75 or less, and further preferably 0.65. It is preferable to have.

The type of the pressure-sensitive adhesive according to the present embodiment is not particularly limited as long as the above physical properties are satisfied, and for example, an acrylic pressure-sensitive adhesive, a polyester-based pressure-sensitive adhesive, a polyurethane-based pressure-sensitive adhesive, a rubber-based pressure-sensitive adhesive, a silicone-based pressure-sensitive adhesive, and the like. It may be any of. Further, the pressure-sensitive adhesive may be an emulsion type, a solvent type or a solvent-free type, and may be either a crosslinked type or a non-crosslinked type. Among them, an acrylic pressure-sensitive adhesive that easily satisfies the above-mentioned physical properties and is excellent in adhesive physical properties, optical properties, and the like is preferable.

Further, the acrylic pressure-sensitive adhesive may be an active energy ray-curable one, an active energy ray non-curable one, or a heat-crosslinkable one. It may be non-crosslinkable or a combination thereof, but it is preferably active energy ray non-curable in order to obtain good flexibility. As the active energy ray non-curable acrylic pressure-sensitive adhesive, a crosslinked type is particularly preferable, and further, a thermally crosslinked type is preferable.

The pressure-sensitive adhesive according to the present embodiment may be particularly referred to as a pressure-sensitive adhesive composition containing the (meth) acrylic acid ester polymer (A) and the cross-linking agent (B) (hereinafter referred to as “adhesive composition P”). It is preferable that the pressure-sensitive adhesive is obtained by cross-linking.). With such an adhesive, it is easy to satisfy the above-mentioned physical properties, and since good adhesive force and a predetermined cohesive force can be obtained, the durability is also excellent. In addition, in this specification, (meth) acrylic acid means both acrylic acid and methacrylic acid. The same applies to other similar terms. In addition, the concept of "polymer" shall be included in "polymer".

(1) Component (1-1) (meth) acrylic acid ester polymer (A) of the adhesive composition P
The (meth) acrylic acid ester polymer (A) is a (meth) acrylic acid alkyl ester and a monomer having a reactive functional group in the molecule (monomer containing a reactive functional group) as a monomer unit constituting the polymer. And are preferably contained.

The (meth) acrylic acid ester polymer (A) can exhibit preferable tackiness by containing the (meth) acrylic acid alkyl ester as the monomer unit constituting the polymer. As the (meth) acrylic acid alkyl ester, a (meth) acrylic acid alkyl ester having an alkyl group having 1 to 20 carbon atoms is preferable. The alkyl group may be linear or branched, or may have a cyclic structure.

The (meth) acrylic acid alkyl ester having an alkyl group having 1 to 20 carbon atoms may be a monomer having a glass transition temperature (Tg) of −40 ° C. or lower as a homopolymer (hereinafter referred to as “low Tg alkyl acrylate”). ) And a monomer having a glass transition temperature (Tg) of more than 0 ° C. as a homopolymer (hereinafter, may be referred to as “high Tg alkyl acrylate”) are preferably used in combination. As a result, the relaxation elastic modulus fluctuation value and the loss tangent of the obtained pressure-sensitive adhesive can easily satisfy the above-mentioned values.

Examples of the low Tg alkyl acrylate include n-butyl acrylate (Tg-55 ° C.), n-octyl acrylate (Tg-65 ° C.), isooctyl acrylate (Tg-58 ° C.), and 2-ethylhexyl acrylate (Tg). -70 ° C), isononyl acrylate (Tg-58 ° C), isodecyl acrylate (Tg-60 ° C), isodecyl methacrylate (Tg-41 ° C), n-lauryl methacrylate (Tg-65 ° C), tridecyl acrylate (Tg −55 ° C.), tridecyl methacrylate (Tg −40 ° C.) and the like are preferably mentioned. Above all, from the viewpoint of more effectively improving the flexibility, the homopolymer Tg of the low Tg alkyl acrylate is more preferably −45 ° C. or lower, and more preferably −50 ° C. or lower. Is particularly preferable. Specifically, n-butyl acrylate and 2-ethylhexyl acrylate are particularly preferable. These may be used alone or in combination of two or more.

Examples of the high Tg alkyl acrylate include methyl acrylate (Tg10 ° C.), methyl methacrylate (Tg105 ° C.), ethyl methacrylate (Tg65 ° C.), n-butyl methacrylate (Tg20 ° C.), and isobutyl methacrylate (Tg48 ° C.). ), T-butyl methacrylate (Tg 107 ° C), n-stearyl acrylate (Tg 30 ° C), n-stearyl methacrylate (Tg 38 ° C), cyclohexyl acrylate (Tg 15 ° C), cyclohexyl methacrylate (Tg 66 ° C), methacrylic acid. Examples thereof include benzyl (Tg 54 ° C.), isobornyl acrylate (Tg 94 ° C.), isobornyl methacrylate (Tg 180 ° C.), adamantyl acrylate (Tg 115 ° C.), adamantyl methacrylate (Tg 141 ° C.), morpholine acrylate (Tg 145 ° C.) and the like. Among the above, methyl acrylate, methyl methacrylate and isobornyl acrylate are preferable from the viewpoint of cohesive force. These may be used alone or in combination of two or more.

The (meth) acrylic acid ester polymer (A) preferably contains low Tg alkyl acrylate as a lower limit value of 50% by mass or more, and particularly 55% by mass or more, as a monomer unit constituting the polymer. Is preferable, and more preferably 60% by mass or more is contained. Further, the (meth) acrylic acid ester polymer (A) preferably contains the above low Tg alkyl acrylate as a monomer unit constituting the polymer in an upper limit of 85% by mass or less, and particularly in an amount of 75% by mass or less. It is preferable that the content is 65% by mass or less.

The (meth) acrylic acid ester polymer (A) preferably contains a high Tg alkyl acrylate as a lower limit value of 5% by mass or more, and particularly 10% by mass or more, as a monomer unit constituting the polymer. It is preferable that the content is 15% by mass or more. Further, the (meth) acrylic acid ester polymer (A) preferably contains the above high Tg alkyl acrylate as a monomer unit constituting the polymer in an upper limit of 30% by mass or less, and particularly in an amount of 25% by mass or less. It is preferable that the content is 20% by mass or less.

The (meth) acrylic acid ester polymer (A) contains a low Tg alkyl acrylate and a high Tg alkyl acrylate at the above-mentioned contents as the monomer unit constituting the polymer, so that the pressure-sensitive adhesive obtained can be relaxed. The elastic modulus fluctuation value and the loss tangent are more likely to satisfy the above-mentioned values.

The (meth) acrylic acid ester polymer (A) contains a reactive functional group-containing monomer as a monomer unit constituting the polymer, and thus via the reactive functional group derived from the reactive functional group-containing monomer. , Will react with the cross-linking agent (B) described later, thereby forming a cross-linked structure (three-dimensional network structure), and a pressure-sensitive adhesive having a desired cohesive force can be obtained.

The reactive functional group-containing monomer contained in the (meth) acrylic acid ester polymer (A) as a monomer unit constituting the polymer includes a monomer having a hydroxyl group in the molecule (monomer containing a hydroxyl group) and carboxy in the molecule. Preferred examples thereof include a monomer having a group (monomer containing a carboxy group) and a monomer having an amino group in the molecule (monomer containing an amino group). These reactive functional group-containing monomers may be used alone or in combination of two or more.

Among the above reactive functional group-containing monomers, hydroxyl group-containing monomers and carboxy group-containing monomers are preferable, and hydroxyl group-containing monomers are particularly preferable. Since the hydroxyl group-containing monomer has a relatively low glass transition temperature (Tg) as a homopolymer, it is easy to maintain high flexibility of the obtained (meth) acrylic acid ester polymer (A).

Examples of the hydroxyl group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and (meth). ) Hydroxyalkyl esters of (meth) acrylic acid such as 3-hydroxybutyl acrylate and 4-hydroxybutyl (meth) acrylic acid can be mentioned. Among them, 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meth) acrylate are preferable from the viewpoint of the flexibility of the obtained (meth) acrylic acid ester polymer (A). These may be used alone or in combination of two or more.

When the (meth) acrylic acid ester polymer (A) contains a hydroxyl group-containing monomer as a monomer unit constituting the polymer, the content of the hydroxyl group-containing monomer is preferably 1% by mass or more, 3 It is more preferably mass% or more, particularly preferably 5 mass% or more, further preferably 10 mass% or more, and most preferably 15 mass% or more. The content of the hydroxyl group-containing monomer is preferably 30% by mass or less, particularly preferably 25% by mass or less, and further preferably 20% by mass or less. When the content of the hydroxyl group-containing monomer is in the above range, the flexibility and adhesiveness of the obtained (meth) acrylic acid ester polymer (A) are improved, and the repeated bending device of the obtained pressure-sensitive adhesive layer is used. The bending state relaxation effect is achieved at a higher level.

The (meth) acrylic acid ester polymer (A) may contain a nitrogen atom-containing monomer as a monomer unit constituting the polymer. Examples of the nitrogen atom-containing monomer include a monomer having an amino group, a monomer having an amide group, a monomer having a nitrogen-containing heterocycle, and the like, and among them, a monomer having a nitrogen-containing heterocycle is preferable.

Examples of the monomer having a nitrogen-containing heterocycle include N- (meth) acryloylmorpholin, N-vinyl-2-pyrrolidone, N- (meth) acryloylpyrrolidone, N- (meth) acryloylpiperidin, and N- (meth) acryloyl. Pyrrolidine, N- (meth) acryloyl azylidine, aziridinyl ethyl (meth) acrylate, 2-vinylpyridine, 4-vinylpyridine, 2-vinylpyrazine, 1-vinylimidazole, N-vinylcarbazole, N-vinylphthalimide, etc. Among them, N- (meth) acryloylmorpholin, which exhibits more excellent adhesive strength, is preferable, and N-acryloylmorpholin is particularly preferable. These may be used alone or in combination of two or more.

When the (meth) acrylic acid ester polymer (A) contains a nitrogen atom-containing monomer as a monomer unit constituting the polymer, the content of the nitrogen atom-containing monomer is preferably 1% by mass or more. In particular, it is preferably 3% by mass or more. The content of the nitrogen atom-containing monomer is preferably 20% by mass or less, particularly preferably 15% by mass or less, and further preferably 10% by mass or less.

If desired, the (meth) acrylic acid ester polymer (A) may contain another monomer as a monomer unit constituting the polymer. As the other monomer, a monomer containing no reactive functional group is preferable so as not to inhibit the above-mentioned action of the reactive functional group-containing monomer. Examples of such monomers include (meth) acrylic acid alkoxyalkyl esters such as methoxyethyl (meth) acrylate and ethoxyethyl (meth) acrylate, vinyl acetate, styrene and the like. These may be used alone or in combination of two or more.

The polymerization mode of the (meth) acrylic acid ester polymer (A) may be a random copolymer or a block copolymer.

The lower limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is preferably 100,000 or more, particularly preferably 300,000 or more, and further preferably 500,000 or more. When the lower limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is the above, the durability of the pressure-sensitive adhesive becomes more excellent. The weight average molecular weight in the present specification is a value in terms of standard polystyrene measured by a gel permeation chromatography (GPC) method.

Further, the upper limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is preferably 1.5 million or less, particularly preferably 1.2 million or less, and further preferably 1 million or less. preferable. When the upper limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is as described above, the flexibility and adhesive strength of the obtained pressure-sensitive adhesive become more excellent.

In the adhesive composition P, the (meth) acrylic acid ester polymer (A) may be used alone or in combination of two or more.

(1-2) Crosslinking agent (B)
The cross-linking agent (B) cross-links the (meth) acrylic acid ester polymer (A) with the heating of the adhesive composition P containing the cross-linking agent (B) as a trigger to form a three-dimensional network structure. .. As a result, the cohesive force of the obtained pressure-sensitive adhesive is improved, and the pressure-sensitive adhesive layer becomes excellent in durability.

The cross-linking agent (B) may be any as long as it reacts with the reactive group of the (meth) acrylic acid ester polymer (A), and for example, an isocyanate-based cross-linking agent, an epoxy-based cross-linking agent, and an amine-based cross-linking agent. , Melamine-based cross-linking agent, aziridine-based cross-linking agent, hydrazine-based cross-linking agent, aldehyde-based cross-linking agent, oxazoline-based cross-linking agent, metal alkoxide-based cross-linking agent, metal chelate-based cross-linking agent, metal salt-based cross-linking agent, ammonium salt-based cross-linking agent, etc. Can be mentioned. Among the above, it is preferable to use an isocyanate-based cross-linking agent having excellent reactivity with a reactive functional group-containing monomer which is a constituent monomer unit of the (meth) acrylic acid ester polymer (A), particularly a hydroxyl group-containing monomer. The cross-linking agent (B) may be used alone or in combination of two or more.

The isocyanate-based cross-linking agent contains at least a polyisocyanate compound. Examples of the polyisocyanate compound include aromatic polyisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate, and xylylene diisocyanate, aliphatic polyisocyanates such as hexamethylene diisocyanate, isophorone diisocyanates, and alicyclic polyisocyanates such as hydrogenated diphenylmethane diisocyanate. , And their biurets, isocyanates, and adducts, which are reactants with low molecular weight active hydrogen-containing compounds such as ethylene glycol, propylene glycol, neopentyl glycol, trimethylolpropane, and castor oil. Of these, trimethylolpropane-modified aromatic polyisocyanates, particularly trimethylolpropane-modified tolylene diisocyanate and trimethylolpropane-modified xylylene diisocyanate, are preferable from the viewpoint of reactivity with hydroxyl groups.

The content of the cross-linking agent (B) in the adhesive composition P is preferably 0.1 part by mass or more with respect to 100 parts by mass of the (meth) acrylic acid ester polymer (A), and particularly 0. It is preferably 4 parts by mass or more, and more preferably 1.0 part by mass or more. The content is preferably 10 parts by mass or less, particularly preferably 8 parts by mass or less, and further preferably 5 parts by mass or less. When the content of the cross-linking agent (B) is within the above range, the cohesive force of the obtained adhesive is appropriate, and the effect of alleviating the bending state of the repeatedly bending device of the obtained adhesive layer is achieved at a high level. To.

(1-3) Various Additives Various additives usually used for acrylic pressure-sensitive adhesives, such as silane coupling agents, ultraviolet absorbers, antistatic agents, and tackifiers, are added to the pressure-sensitive adhesive composition P, if desired. Agents, antioxidants, light stabilizers, softeners, fillers, refractive index adjusters and the like can be added. The polymerization solvent and the diluting solvent described later are not included in the additives constituting the adhesive composition P.

(2) Production of Adhesive Composition P The adhesive composition P produces a (meth) acrylic acid ester polymer (A), and the obtained (meth) acrylic acid ester polymer (A) and a cross-linking agent. It can be produced by mixing with (B) and adding an additive if desired.

The (meth) acrylic acid ester polymer (A) can be produced by polymerizing a mixture of monomers constituting the polymer by an ordinary radical polymerization method. The polymerization of the (meth) acrylic acid ester polymer (A) is preferably carried out by a solution polymerization method using a polymerization initiator, if desired. Examples of the polymerization solvent include ethyl acetate, n-butyl acetate, isobutyl acetate, toluene, acetone, hexane, methyl ethyl ketone and the like, and two or more of them may be used in combination.

Examples of the polymerization initiator include azo compounds and organic peroxides, and two or more of them may be used in combination. Examples of the azo compound include 2,2'-azobisisobutyronitrile, 2,2'-azobis (2-methylbutyronitrile), 1,1'-azobis (cyclohexane1-carbonitrile), and 2, , 2'-azobis (2,4-dimethylvaleronitrile), 2,2'-azobis (2,4-dimethyl-4-methoxyvaleronitrile), dimethyl 2,2'-azobis (2-methylpropionate) 4,4'-azobis (4-cyanovaleric acid), 2,2'-azobis (2-hydroxymethylpropionitrile), 2,2'-azobis [2- (2-imidazolin-2-yl) Propane] and the like.

Examples of the organic peroxide include benzoyl peroxide, t-butyl perbenzoate, cumene hydroperoxide, diisopropyl peroxydicarbonate, di-n-propyl peroxydicarbonate, and di (2-ethoxyethyl) peroxy. Examples thereof include dicarbonate, t-butylperoxyneodecanoate, t-butylperoxyvivarate, (3,5,5-trimethylhexanoyl) peroxide, dipropionyl peroxide, diacetyl peroxide and the like.

In the above polymerization step, the weight average molecular weight of the obtained polymer can be adjusted by adding a chain transfer agent such as 2-mercaptoethanol.

Once the (meth) acrylic acid ester polymer (A) is obtained, the cross-linking agent (B) and, if desired, an additive and a diluting solvent are sufficiently added to the solution of the (meth) acrylic acid ester polymer (A). To obtain a tacky composition P (coating solution) diluted with a solvent.

If any of the above components is in the form of a solid, or if precipitation occurs when the components are mixed with other components in an undiluted state, the components are used alone in a diluted solvent in advance. It may be dissolved or diluted and then mixed with other ingredients.

Examples of the diluting solvent include aliphatic hydrocarbons such as hexane, heptane and cyclohexane, aromatic hydrocarbons such as toluene and xylene, halogenated hydrocarbons such as methylene chloride and ethylene chloride, methanol, ethanol, propanol and butanol. Alcohols such as 1-methoxy-2-propanol, ketones such as acetone, methyl ethyl ketone, 2-pentanone, isophorone, cyclohexanone, esters such as ethyl acetate and butyl acetate, and cellosolve solvents such as ethyl cellosolve are used.

The concentration and viscosity of the coating solution prepared in this manner may be any range as long as it can be coated, and may be appropriately selected depending on the situation. For example, the adhesive composition P is diluted to a concentration of 10 to 60% by mass. It should be noted that the addition of a diluting solvent or the like is not a necessary condition when obtaining the coating solution, and the diluting solvent may not be added as long as the adhesive composition P has a viscosity that allows coating. In this case, the adhesive composition P becomes a coating solution using the polymerization solvent of the (meth) acrylic acid ester polymer (A) as it is as a diluting solvent.

(3) Production of Adhesive The adhesive according to the present embodiment is preferably obtained by cross-linking the adhesive composition P. Crosslinking of the adhesive composition P can usually be carried out by heat treatment. It should be noted that this heat treatment can also be used as a drying treatment for volatilizing the diluting solvent or the like from the coating film of the adhesive composition P applied to the desired object.

The heating temperature of the heat treatment is preferably 50 to 150 ° C, particularly preferably 70 to 120 ° C. The heating time is preferably 10 seconds to 10 minutes, and particularly preferably 50 seconds to 2 minutes.

After the heat treatment, if necessary, a curing period of about 1 to 2 weeks may be provided at room temperature (for example, 23 ° C., 50% RH). If this curing period is required, the adhesive is formed after the curing period has elapsed, and if the curing period is not required, the adhesive is formed after the heat treatment is completed.

By the above heat treatment (and curing), the (meth) acrylic acid ester polymer (A) is sufficiently cross-linked via the cross-linking agent (B) to form a cross-linked structure, and a pressure-sensitive adhesive is obtained. Such a pressure-sensitive adhesive has a predetermined cohesive force.

(4) Physical Properties of Adhesive The storage elastic modulus (G') of the adhesive according to the present embodiment at 25 ° C. is preferably 0.01 MPa or more as a lower limit. The upper limit of the storage elastic modulus (G') is preferably 0.25 MPa or less, and particularly preferably 0.20 MPa or less.

The elastic modulus (G ") of the pressure-sensitive adhesive according to this embodiment at 25 ° C. is preferably 0.005 MPa or more, particularly preferably 0.01 MPa or more, as a lower limit value. The upper limit of the loss elastic modulus (G ″) is preferably 0.1 MPa or less, and particularly preferably 0.08 MPa or less.

When the storage elastic modulus (G') and the loss elastic modulus (G ") of the pressure-sensitive adhesive according to the present embodiment are in the above ranges, the adhesive strength to the flexible member becomes more excellent, and the durability of the repeatedly bending device becomes durable. The properties are improved. The methods for measuring the storage elastic modulus (G') and the loss elastic modulus (G ") are as shown in the test examples described later.

[Adhesive sheet]
The pressure-sensitive adhesive sheet according to the present embodiment has a pressure-sensitive adhesive layer for adhering one flexible member constituting the repeatedly bending device to another flexible member, and the pressure-sensitive adhesive layer is the above-mentioned pressure-sensitive adhesive. It consists of.

FIG. 1 shows a specific configuration as an example of the pressure-sensitive adhesive sheet according to the present embodiment.
As shown in FIG. 1, the pressure-sensitive adhesive sheet 1 according to the embodiment is in contact with the two release sheets 12a and 12b and the release surfaces of the two release sheets 12a and 12b. , 12b and the pressure-sensitive adhesive layer 11. The peeling surface of the release sheet in the present specification refers to a surface having peelability in the release sheet, and includes both a surface subjected to peeling treatment and a surface exhibiting peelability even without peeling treatment. ..

(1) Components (1-1) Adhesive Layer The adhesive layer 11 is composed of the adhesive according to the above-described embodiment, and is preferably composed of a pressure-sensitive adhesive obtained by cross-linking the adhesive composition P. ..

The thickness of the pressure-sensitive adhesive layer 11 (value measured according to JIS K7130) in the pressure-sensitive adhesive sheet 1 according to the present embodiment is preferably 2 μm or more, particularly preferably 5 μm or more, and further preferably 5 μm or more as a lower limit value. It is preferably 10 μm or more. When the lower limit of the thickness of the pressure-sensitive adhesive layer 11 is the above, it is easy to exert a desired adhesive force, and it is possible to effectively suppress the occurrence of floating and peeling due to repeated bending. The thickness of the pressure-sensitive adhesive layer 11 is preferably 150 μm or less, more preferably 100 μm or less, particularly preferably 70 μm or less, and further preferably 50 μm or less as an upper limit value. When the upper limit of the thickness of the pressure-sensitive adhesive layer 11 is the above, it is possible to suppress the seepage of the pressure-sensitive adhesive or the components constituting the pressure-sensitive adhesive from the pressure-sensitive adhesive layer due to repeated bending. The pressure-sensitive adhesive layer 11 may be formed as a single layer, or may be formed by laminating a plurality of layers.

(1-2) Release Sheet The release sheets 12a and 12b protect the pressure-sensitive adhesive layer 11 until the pressure-sensitive adhesive sheet 1 is used, and are peeled off when the pressure-sensitive adhesive sheet 1 (adhesive layer 11) is used. In the pressure-sensitive adhesive sheet 1 according to the present embodiment, one or both of the release sheets 12a and 12b are not always necessary.

Examples of the release sheets 12a and 12b include polyethylene film, polypropylene film, polybutene film, polybutadiene film, polymethylpentene film, polyvinyl chloride film, vinyl chloride copolymer film, polyethylene terephthalate film, polyethylene naphthalate film, and polybutylene. Telephthalate film, polyurethane film, ethylene vinyl acetate film, ionomer resin film, ethylene / (meth) acrylic acid copolymer film, ethylene / (meth) acrylic acid ester copolymer film, polystyrene film, polycarbonate film, polyimide film, fluorine A resin film or the like is used. In addition, these crosslinked films are also used. Further, these laminated films may be used.

It is preferable that the peeling surface (particularly the surface in contact with the pressure-sensitive adhesive layer 11) of the peeling sheets 12a and 12b is subjected to a peeling treatment. Examples of the release agent used in the release treatment include alkyd-based, silicone-based, fluorine-based, unsaturated polyester-based, polyolefin-based, and wax-based release agents. Of the release sheets 12a and 12b, it is preferable that one of the release sheets is a heavy release type release sheet having a large release force and the other release sheet is a light release type release sheet having a small release force.

The thickness of the release sheets 12a and 12b is not particularly limited, but is usually about 20 to 150 μm.

(2) Production of Adhesive Sheet As an example of production of the adhesive sheet 1, a case where the adhesive composition P is used will be described. The coating liquid of the adhesive composition P is applied to the peeling surface of one of the release sheets 12a (or 12b), heat-treated to heat-crosslink the adhesive composition P to form a coating layer, and then the coating thereof. The peeling surface of the other peeling sheet 12b (or 12a) is superposed on the layer. When the curing period is required, the curing period is set, and when the curing period is not required, the coating layer becomes the adhesive layer 11 as it is. As a result, the adhesive sheet 1 is obtained. The conditions for heat treatment and curing are as described above.

As another production example of the pressure-sensitive adhesive sheet 1, a coating liquid of the pressure-sensitive adhesive composition P is applied to the peel-off surface of one of the release sheets 12a, heat-treated to heat-crosslink the pressure-sensitive adhesive composition P, and the coating layer is formed. To obtain a release sheet 12a with a coating layer. Further, the coating liquid of the adhesive composition P is applied to the peeling surface of the other release sheet 12b, heat-treated to heat-crosslink the adhesive composition P to form a coating layer, and the coating layer is attached. To obtain the release sheet 12b of. Then, the release sheet 12a with the coating layer and the release sheet 12b with the coating layer are bonded so that both coating layers are in contact with each other. When the curing period is required, the curing period is set, and when the curing period is not required, the above-mentioned laminated coating layer becomes the pressure-sensitive adhesive layer 11. As a result, the adhesive sheet 1 is obtained. According to this production example, even when the pressure-sensitive adhesive layer 11 is relatively thick, stable production is possible.

As a method for applying the coating liquid of the adhesive composition P, for example, a bar coating method, a knife coating method, a roll coating method, a blade coating method, a die coating method, a gravure coating method and the like can be used.

(3) Adhesive strength The adhesive strength of the adhesive sheet 1 according to the present embodiment to soda lime glass is preferably 5.1 N / 25 mm or more as a lower limit value, and particularly preferably 5.5 N / 25 mm or more. Further, it is preferably 6.0 N / 25 mm or more. When the adhesive strength of the adhesive sheet 1 is 5.1 N / 25 mm or more, the interface peeling suppressing effect becomes more excellent. On the other hand, the upper limit of the adhesive strength is not particularly limited, but is usually preferably 25 N / 25 mm or less, more preferably 20 N / 25 mm or less, and particularly preferably 15 N / 25 mm or less. The adhesive strength basically refers to the adhesive strength measured by the 180-degree peeling method according to JIS Z0237: 2009, and the specific test method is as shown in the test example described later.

[Repeatly bent laminated member]
As shown in FIG. 2, the repetitive bending laminated member 2 according to the present embodiment includes a first flexible member 21 (one flexible member) and a second flexible member 22 (another flexible member). , Which is located between them and comprises an adhesive layer 11 that attaches the first flexible member 21 and the second flexible member 22 to each other.

The pressure-sensitive adhesive layer 11 in the repeatedly bent laminated member 2 is the pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet 1 described above.

The repetitive bending laminated member 2 is a repetitive bending device itself or a member constituting a part of the repetitive bending device. The repetitive bending device is preferably, but is not limited to, a display capable of repeated bending (including bending). Examples of the repetitive bending device include an organic electroluminescence (organic EL) display, an electrophoretic display (electronic paper), a flexible printed substrate, a liquid crystal display using a plastic substrate (film) as a substrate, a foldable display, and the like. It may be a touch panel.

The first flexible member 21 and the second flexible member 22 are members capable of repeated bending (including bending), and are, for example, a cover film, a barrier film, a polarizing film, a splitter, a retardation film, and the like. Viewing angle compensation film, brightness improvement film, contrast improvement film, diffusion film, semi-transmissive reflective film, electrode film, transparent conductive film, metal mesh film, film sensor, liquid crystal polymer film, light emitting polymer film, film-like liquid crystal module, organic Examples thereof include an EL module (organic EL film) and an electronic paper module (film-like electronic paper).

Among the above, at least one of the first flexible member 21 and the second flexible member 22 is a display element that can be repeatedly bent, specifically, a liquid crystal polymer film, a light emitting polymer film, a film-shaped liquid crystal module, and an organic material. An EL module (organic EL film) or an electronic paper module (film-like electronic paper) is preferable.

The Young's modulus of the first flexible member 21 and the second flexible member 22 is preferably 0.1 to 10 GPa, particularly preferably 0.5 to 7 GPa, and further preferably 1.0 to 1.0 GPa, respectively. It is preferably 5 GPa. When the Young's modulus of the first flexible member 21 and the second flexible member 22 is within such a range, it becomes easy to repeatedly bend each flexible member.

The thickness of the first flexible member 21 and the second flexible member 22 is preferably 5 to 3000 μm, particularly preferably 10 to 1000 μm, and further preferably 10 to 500 μm. .. When the thickness of the first flexible member 21 and the second flexible member 22 is within such a range, it becomes easy to repeatedly bend each flexible member.

In order to manufacture the repeatedly bent laminated member 2, as an example, one of the release sheets 12a of the pressure-sensitive adhesive sheet 1 is peeled off, and the exposed pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet 1 is removed from one of the first flexible members 21. Adhere to the surface of.

After that, the other release sheet 12b is peeled off from the pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet 1, the exposed pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet 1 and the second flexible member 22 are bonded to each other, and the bending laminated member 2 is repeatedly bent. To get. Further, as another example, the bonding order of the first flexible member 21 and the second flexible member 22 may be changed.

[Repeat bending device]
The repetitive bending device according to the present embodiment includes the repetitive bending laminated member 2 described above, and may be composed of only the repetitive bending laminated member 2, one or a plurality of repetitive bending laminated members 2, and another. It may be configured to include a flexible member. When laminating one repeatedly bent laminated member 2 and another repeatedly bent laminated member 2, or when laminating the repeatedly bent laminated member 2 and another flexible member, the adhesive layer 11 of the adhesive sheet 1 described above is used. It is preferable to stack the layers through the layers.

In the repetitive bending device according to the present embodiment, since the pressure-sensitive adhesive layer is made of the above-mentioned adhesive, when it is repeatedly bent (for example, 30,000 times) and when it is left in a bent state for a long period of time (for example, at least 24 hours or more). In the above, after being released from the bent state, the repeatedly bent device is suppressed from being solidified in a greatly bent state, and the influence of the repeated bending and the influence of being placed in the bending state are alleviated. The effect of relaxing the bending state of the repeated bending device can be evaluated, for example, by the amount of static bending deformation by the static bending test and the amount of dynamic bending deformation by the dynamic bending test.

In the static bending test, a laminated body in which an adhesive layer (thickness: 12 μm) is sandwiched between two polyethylene terephthalate films (thickness: 12 μm) and a size of 200 mm × 50 mm is tested. Make a piece. As shown in FIG. 3, this test piece S is held in an environment of 23 ° C. and 50% RH for 24 hours in a bent state between a holding plate P made of two glass plates erected. .. At this time, the distance between the two holding plates P is set to 6 mm (bending diameter of the test piece S: 6 mmφ), and the substantially central portion of the long side (200 mm) of the test piece S becomes the bent part. The test piece S is held so that both short sides (50 mm) of S are located on the upper side. After performing this static bending test, the test piece S is taken out from between the two holding plates P, and as shown in FIG. 4, the test piece S is placed on a flat plate so that the convex direction of the bent portion is on the upper side. Place on. Then, immediately after the test, 30 minutes after the test, and 24 hours after the test, the height h from the flat plate surface to the apex of the bent portion (deformed portion) is measured as the static bending deformation amount. This static bending deformation amount can be used as the test result of the static bending test, and the bending state relaxation effect can be evaluated based on the static bending deformation amount.

Immediately after the test, the amount of static bending deformation by the static bending test is preferably 3 mm or less, particularly preferably 1 mm or less, and further preferably 0.5 mm or less. Further, after 30 minutes from the test, it is preferably 1 mm or less, and particularly preferably 0.5 mm or less. Further, after 24 hours of the test, it is preferably 0.5 mm or less, and particularly preferably 0.3 mm or less. The lower limit of any static bending deformation amount is preferably 0 mm.

On the other hand, in the dynamic bending test, it is a laminated body in which an adhesive layer (thickness: 12 μm) is sandwiched between two polyethylene terephthalate films (thickness: 12 μm) and has a size of 150 mm × 50 mm. Is used as a test piece. As shown in FIG. 5, the test piece S is held between two holding plates P of the surface state no-load U-shaped expansion / contraction tester in an environment of 23 ° C. and 50% RH. One of the two holding plates P maintains a parallel relationship with the other holding plate P, and can move back and forth between the other holding plate P and the other holding plate P. The distance between the two holding plates P shall be varied from 86 mm to 6 mm (bending diameter of test piece S: 6 mmφ, stroke: 80 mm). The test piece S is fixed to the holding plate P so that the substantially central portion of the long side (150 mm) thereof becomes a bent portion and both short sides (50 mm) of the test piece S are located on the upper side. In that state, the test piece S is bent 30,000 times at a bending speed (reciprocating speed of the holding plate P) of 30 rpm. After performing this dynamic bending test, the test piece S is taken out from between the two holding plates P, and as shown in FIG. 4, the test piece S is placed on a flat plate so that the convex direction of the bent portion is on the upper side. Place it. Then, immediately after the test and 24 hours after the test, the height h from the surface of the flat plate to the apex of the bent portion (deformed portion) is measured as the amount of dynamic bending deformation. This dynamic bending deformation amount can be used as the test result of the dynamic bending test, and the bending state relaxation effect can be evaluated based on the dynamic bending deformation amount.

Immediately after the test, the amount of dynamic bending deformation by the dynamic bending test is preferably 3 mm or less, particularly preferably 1 mm or less, and further preferably 0.5 mm or less. Further, after 24 hours of the test, it is preferably 1 mm or less, and particularly preferably 0.5 mm or less. The lower limit of any of the dynamic bending deformation amounts is preferably 0 mm.

The embodiments described above are described for facilitating the understanding of the present invention, and are not described for limiting the present invention. Therefore, each element disclosed in the above embodiment is intended to include all design changes and equivalents belonging to the technical scope of the present invention.

For example, either or both of the release sheets 12a and 12b in the pressure-sensitive adhesive sheet 1 may be omitted, or a desired flexible member may be laminated in place of the release sheets 12a and / or 12b.

Hereinafter, the present invention will be described in more detail with reference to Examples and the like, but the scope of the present invention is not limited to these Examples and the like.

[Example 1]
1. 1. Preparation of (meth) acrylic acid ester polymer (A) Solution polymerization method of 65 parts by mass of 2-ethylhexyl acrylate, 5 parts by mass of N-acryloylmorpholine, 15 parts by mass of isobonyl acrylate and 15 parts by mass of 2-hydroxyethyl acrylate. The (meth) acrylic acid ester polymer (A) was prepared by copolymerizing with the above. When the molecular weight of this (meth) acrylic acid ester polymer (A) was measured by the method described later, the weight average molecular weight (Mw) was 500,000.

2. 2. Preparation of Adhesive Composition 100 parts by mass (solid content conversion value; the same applies hereinafter) of the (meth) acrylic acid ester polymer (A) obtained in the above step 1 and a trimethylolpropane-modified bird as a cross-linking agent (B). Mix 1.20 parts by mass of range isocyanate (manufactured by Toyochem Co., Ltd., product name "BHS8515"), stir well, and dilute with methyl ethyl ketone (MEK) to obtain a coating solution (solid content) of the adhesive composition. Concentration: 30.0% by mass) was obtained.

3. 3. Manufacture of Adhesive Sheet A heavy release type release sheet (manufactured by Lintec Corporation, product name "SP-PET382150") in which one side of a polyethylene terephthalate film is peeled off with a silicone-based release agent from the coating solution of the adhesive composition obtained in the above step 2. ”) Was applied to the peeled surface with a comma coater. Then, the coated layer was heat-treated at 90 ° C. for 1 minute to form a coated layer.

Next, a light release type release sheet (manufactured by Lintec Corporation, product name "SP-PET38131") in which the coating layer on the heavy release type release sheet obtained above and one side of the polyethylene terephthalate film were peeled off with a silicone-based release agent). The adhesive layer having a thickness of 12 μm was formed by laminating the light peeling type peeling sheet so that the peeled surface of the light peeling type peeling sheet was in contact with the coating layer and curing it under the conditions of 23 ° C. and 50% RH for 7 days. A pressure-sensitive adhesive sheet having a structure, that is, a heavy-release type release sheet / a pressure-sensitive adhesive layer (thickness: 12 μm) / a light-release type release sheet, was produced. The thickness of the pressure-sensitive adhesive layer is a value measured using a constant pressure thickness measuring device (manufactured by Teclock Co., Ltd., product name "PG-02") in accordance with JIS K7130.

[Example 2]
60 parts by mass of 2-ethylhexyl acrylate, 20 parts by mass of methyl methacrylate and 20 parts by mass of 2-hydroxyethyl acrylate were copolymerized by a solution polymerization method to prepare a (meth) acrylic acid ester polymer (A). When the molecular weight of this (meth) acrylic acid ester polymer (A) was measured by the method described later, the weight average molecular weight (Mw) was 600,000.

100 parts by mass of the (meth) acrylic acid ester polymer (A) obtained above and 0.47 parts by mass of trimethylolpropane-modified tolylene diisocyanate (manufactured by Toyochem, product name "BHS8515") as a cross-linking agent (B). The parts were mixed with each other, sufficiently stirred, and diluted with MEK to obtain a coating solution (solid content concentration: 30.0% by mass) of the adhesive composition. A pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 using the coating solution of the obtained pressure-sensitive adhesive composition.

[Example 3]
60 parts by mass of butyl acrylate, 20 parts by mass of methyl acrylate and 20 parts by mass of 2-hydroxyethyl acrylate were copolymerized by a solution polymerization method to prepare a (meth) acrylate ester polymer (A). When the molecular weight of this (meth) acrylic acid ester polymer (A) was measured by the method described later, the weight average molecular weight (Mw) was 600,000.

100 parts by mass of the (meth) acrylic acid ester polymer (A) obtained above and 0.47 parts by mass of trimethylolpropane-modified tolylene diisocyanate (manufactured by Toyochem, product name "BHS8515") as a cross-linking agent (B). The parts were mixed with each other, sufficiently stirred, and diluted with MEK to obtain a coating solution (solid content concentration: 30.0% by mass) of the adhesive composition. A pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 using the coating solution of the obtained pressure-sensitive adhesive composition.

[Example 4]
Using the (meth) acrylic acid ester polymer (A) prepared in Example 3, the pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 except that the blending amount of the cross-linking agent (B) was changed to 0.94 parts by mass. Made.

[Example 5]
Using the (meth) acrylic acid ester polymer (A) prepared in Example 2, the pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 except that the blending amount of the cross-linking agent (B) was changed to 0.94 parts by mass. Made.

[Example 6]
Using the (meth) acrylic acid ester polymer (A) prepared in Example 2, the pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 except that the blending amount of the cross-linking agent (B) was changed to 1.88 parts by mass. Made.

[Example 7]
Using the (meth) acrylic acid ester polymer (A) prepared in Example 1, the pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 except that the blending amount of the cross-linking agent (B) was changed to 0.60 parts by mass. Made.

[Comparative Example 1]
47.8 parts by mass of 2-ethylhexyl acrylate, 47.8 parts by mass of n-butyl acrylate, 4 parts by mass of acrylic acid and 0.4 parts by mass of 2-hydroxypropyl acrylate were copolymerized by a solution polymerization method. Meta) Acrylic acid ester polymer (A) was prepared. When the molecular weight of this (meth) acrylic acid ester polymer (A) was measured by the method described later, the weight average molecular weight (Mw) was 600,000.

100 parts by mass of the (meth) acrylic acid ester polymer (A) obtained above and trimethylolpropane-modified tolylene diisocyanate (manufactured by Toyochem, product name "BHS8515") 3.75% by mass as a cross-linking agent (B). The parts were mixed with each other, sufficiently stirred, and diluted with MEK to obtain a coating solution (solid content concentration: 30.0% by mass) of the adhesive composition. A pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 using the coating solution of the obtained pressure-sensitive adhesive composition.

[Comparative Example 2]
Using the (meth) acrylic acid ester polymer (A) prepared in Example 3, the pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 except that the blending amount of the cross-linking agent (B) was changed to 1.88 parts by mass. Made.

[Comparative Example 3]
Using the (meth) acrylic acid ester polymer (A) prepared in Comparative Example 1, the pressure-sensitive adhesive sheet was prepared in the same manner as in Example 1 except that the blending amount of the cross-linking agent (B) was changed to 6.56 parts by mass. Made.

In Table 1, the composition of the (meth) acrylic acid ester polymer (A) and the blending amount of the cross-linking agent (B) in each Example / Comparative Example (100 mass by mass of the (meth) acrylic acid ester polymer (A)). The mass part with respect to the part) is described. The abbreviations in Table 1 are as follows.
2EHA: 2-ethylhexyl acrylate ACMO: N-acryloylmorpholin IBXA: isobornyl acrylate HEA: 2-hydroxyethyl acrylate MMA: methyl methacrylate BA: n-butyl acrylate MA: methyl acrylate AA: acrylic acid 2HPA: acrylic 2-Hydroxypropyl acid

[Test Example 1] (Measurement of relaxed modulus)
A plurality of adhesive layers of the pressure-sensitive adhesive sheets produced in Examples and Comparative Examples were laminated to form a laminated body having a thickness of 0.5 mm. A cylinder (height 0.5 mm) having a diameter of 8 mm was punched out from the obtained laminated body of the pressure-sensitive adhesive layer, and this was used as a sample.

For the above sample, in accordance with JIS K7424-1, using a viscoelasticity measuring device (manufactured by Antoniopaar, product name "MCR302"), the adhesive was continuously distorted by 10% under the following conditions, and the relaxation elastic modulus G. (T) (MPa) was measured. From the measurement result, the maximum relaxation elastic modulus G (t) _max (MPa) is derived, and the minimum relaxation elastic modulus G measured within 3757 seconds after the maximum relaxation elastic modulus G (t) _max is measured. (T) _min (MPa) was derived.
Measurement temperature: 25 ° C
Measurement points: 1000 points (logarithmic plot)

From the obtained maximum relaxation elastic modulus G (t) _max (MPa) and minimum relaxation elastic modulus G (t) _min (MPa), the relaxation elastic modulus fluctuation value Δlog G (t) is calculated based on the following formula (I). Calculated. The results are shown in Table 1.
ΔlogG (t) = logG (t) _max -logG (t) _min ... (I)

[Test Example 2] (Measurement of dynamic elastic modulus)
A plurality of adhesive layers of the pressure-sensitive adhesive sheets produced in Examples and Comparative Examples were laminated to form a laminated body having a thickness of about 0.5 mm. A cylinder (height 0.5 mm) having a diameter of 8 mm was punched out from the obtained laminated body of the pressure-sensitive adhesive layer, and this was used as a sample.

For the above sample, the dynamic viscoelasticity was measured under the following conditions using a viscoelasticity measuring device (manufactured by Antoniopaar, product name "MCR302") in accordance with JIS K7424-1, and the loss positive contact at 25 ° C. ( Tanδ), storage elastic modulus (G') (MPa) and loss elastic modulus (G ″) (MPa) were observed. The results are shown in Table 1.
Measurement frequency: 1Hz
Measurement temperature range: -20 to 150 ° C

[Test Example 3] (Static bending test)
In an environment of 23 ° C. and 50% RH, the light peeling type peeling sheet was peeled off from the pressure-sensitive adhesive sheets produced in Examples and Comparative Examples, and the exposed pressure-sensitive adhesive layer was formed into a polyethylene terephthalate film (manufactured by Toray Industries, Inc., product name " S10 rumirror ”, thickness: 12 μm) was affixed to one surface. Next, the heavy release type release sheet was peeled off, and the exposed pressure-sensitive adhesive layer was attached to one surface of another polyethylene terephthalate film (manufactured by Toray Industries, Inc., product name "S10 Lumirror", thickness: 12 μm). Then, after pressurizing with an autoclave manufactured by Kurihara Seisakusho at 0.5 MPa and 50 ° C. for 20 minutes, the mixture was left to stand for 24 hours under the conditions of 23 ° C. and 50% RH. The laminate composed of the PET film / adhesive layer / PET film thus obtained was cut into a size of 200 mm × 50 mm, and this was used as a test piece.

The obtained test piece was bent between two standing plates (distance between each other: 6 mm) consisting of two glass plates erected as shown in FIG. 3 in an environment of 23 ° C. and 50% RH. It was held in the state for 24 hours. After performing this static bending test, as shown in FIG. 4, the test piece was placed on a flat plate, and immediately after the test, 30 minutes after the test, and 24 hours after the test, the bent portion (deformed portion) was formed from the surface of the flat plate. The height h to the apex portion was measured as the amount of static bending deformation. Based on the measured amount of static bending deformation, the static bending property was evaluated according to the following criteria. Further, in the test piece after the test, it was visually confirmed whether or not the interface between the adhesive layer and the adherend at the bent portion was peeled off. The results are shown in Table 1.
⊚: Deformation amount immediately after bending test is 1 mm or less 〇: Deformation amount immediately after bending test is more than 1 mm, 3 mm or less, deformation amount after 30 minutes of test is 1 mm or less Δ: Deformation amount immediately after bending test is more than 3 mm, 6 mm or less , Deformation amount after 30 minutes of test is 5 mm or less, Deformation amount after 24 hours of test is 1 mm or less ×: Other than the above

[Test Example 4] (Dynamic bending test)
The laminate composed of the PET film / adhesive layer / PET film obtained in the same manner as in Test Example 3 was cut into 150 mm × 50 mm, and this was used as a test piece. As shown in FIG. 5, both ends of the obtained test piece were fixed to two holding plates of a surface state no-load U-shaped expansion / contraction tester (manufactured by Yuasa System Equipment Co., Ltd., product name "DLDMLH-FS"). Then, the test piece was bent 30,000 times at a bending diameter of 6 mmφ, a stroke of 80 mm, and a bending speed of 30 rpm in an environment of 23 ° C. and 50% RH.

After performing the above dynamic bending test, as shown in FIG. 4, the test piece is placed on a flat plate, and immediately after the test and 24 hours after the test, from the surface of the flat plate to the apex of the bent portion (deformed portion). The height h was measured as the amount of dynamic bending deformation. Based on the measured amount of dynamic bending deformation, the dynamic bending property was evaluated according to the following criteria. Further, in the test piece after the test, it was visually confirmed whether or not the interface between the adhesive layer and the adherend at the bent portion was peeled off. The results are shown in Table 1.
⊚: Deformation amount immediately after bending test is 0 mm
〇: The amount of deformation immediately after the bending test is 1 mm or less, and the amount of deformation 24 hours after the test is 0 mm.
Δ: Deformation amount immediately after the bending test is more than 1 mm and 3 mm or less, and deformation amount after 24 hours of the test is 1 mm or less ×: Other than the above

[Test Example 5] (Measurement of adhesive strength)
The light release type release sheet is peeled off from the adhesive sheets produced in Examples and Comparative Examples, and the exposed adhesive layer is a polyethylene terephthalate (PET) film having an easy adhesive layer (manufactured by Toyobo Co., Ltd., product name "PET A4300", It was bonded to an easy-adhesive layer having a thickness (thickness: 100 μm) to obtain a laminated body of a heavy release type release sheet / adhesive layer / PET film. The obtained laminate was cut into a width of 25 mm and a length of 100 mm.

In an environment of 23 ° C. and 50% RH, the heavy release type release sheet was peeled off from the above laminate, and the exposed adhesive layer was attached to soda lime glass (manufactured by Nippon Sheet Glass Co., Ltd.), and then 23 ° C. and 50% RH. After leaving it for 30 minutes in the above environment, a laminate of PET film and adhesive layer was prepared using a tensile tester (Orientec Co., Ltd., Tencilon) under the conditions of a peeling speed of 300 mm / min and a peeling angle of 180 degrees. The adhesive strength (N / 25 mm) when peeled from the soda lime glass was measured. Conditions other than those described here were measured in accordance with JIS Z0237: 2009. The results are shown in Table 1.

As can be seen from Table 1, the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet of the example is excellent in the bending state alleviating effect when two flexible members are bonded and repeatedly bent and when left in a bending state for a long time. At the same time, it was also excellent in the effect of suppressing interfacial peeling.

INDUSTRIAL APPLICABILITY The present invention is suitable for bonding one flexible member (for example, various films) constituting a repetitive bending device to another flexible member (for example, a display element).

1 ... Adhesive sheet 11 ... Adhesive layer 12a, 12b ... Peeling sheet 2 ... Repeated bending laminated member 21 ... First flexible member 22 ... Second flexible member S ... Test piece P ... Holding plate

Claims (7)

An adhesive for a repetitive bending device for adhering one flexible member constituting a device to be repeatedly bent to another flexible member.
The pressure-sensitive adhesive is a pressure-sensitive adhesive obtained by cross-linking a pressure-sensitive adhesive composition containing a (meth) acrylic acid ester polymer (A) polymerized by a solution polymerization method and a cross-linking agent (B).
In accordance with JIS K7424-1, the maximum relaxation elastic modulus value measured when the pressure-sensitive adhesive is distorted by 10% is set to the maximum relaxation elastic modulus G (t) max (MPa), and the maximum relaxation elastic modulus is defined as the maximum relaxation elastic modulus. The pressure-sensitive adhesive is continuously distorted by 10% until 3757 seconds after G (t) max is measured, and the minimum relaxation modulus value measured during that period is defined as the minimum relaxation modulus G (t) min (MPa). , The relaxation elastic modulus fluctuation value Δlog G (t) calculated from the following equation (I) is 0.85 or less.
The loss tangent (tan δ) at 25 ° C. obtained from the dynamic viscoelasticity measurement according to JIS K7424-1 is 0.328 or more and 0.85 or less.
A pressure-sensitive adhesive for a repetitive bending device, characterized in that the storage elastic modulus (G') at 25 ° C. is 0.01 MPa or more and 0.098 MPa or less.
ΔlogG (t) = logG (t) _max -logG (t) _min ... (I) The pressure-sensitive adhesive for a repetitive bending device according to claim 1, wherein the loss elastic modulus (G ") at 25 ° C. is 0.005 MPa or more and 0.1 MPa or less. An adhesive sheet having an adhesive layer for adhering one flexible member and another flexible member constituting a device that is repeatedly bent.
A pressure-sensitive adhesive sheet, wherein the pressure-sensitive adhesive layer comprises the pressure-sensitive adhesive for a repetitive bending device according to claim 1 or 2. The adhesive sheet comprises two release sheets.
The pressure-sensitive adhesive sheet according to claim 3, wherein the pressure-sensitive adhesive layer is sandwiched between the peel-off sheets so as to be in contact with the peel-off surfaces of the two release sheets. With one flexible member and another flexible member constituting a device that is repeatedly bent,
It is a repetitive bending laminated member provided with an adhesive layer for bonding the one bending member and the other bending member to each other.
A repeatedly bent laminated member, wherein the pressure-sensitive adhesive layer is the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet according to claim 3. The repetitive bending laminated member according to claim 5, wherein at least one of the one bending member and the other bending member is a display element. A repetitive bending device comprising the repetitive bending laminated member according to claim 5 or 6.

Images