WO2022176887A1

WO2022176887A1 - Easily dismantlable bonding material, bonded body, and dismantling method

Info

Publication number: WO2022176887A1
Application number: PCT/JP2022/006093
Authority: WO
Inventors: 絵理子佐藤; 耕三伊藤; 翔太安藤; 皓一眞弓
Original assignee: 国立大学法人九州大学
Priority date: 2021-02-18
Filing date: 2022-02-16
Publication date: 2022-08-25
Also published as: JP2022126154A; JP7248328B2

Abstract

An easily dismantlable bonding material which can be used in a use application that a first structural member is bonded to a second structural member to produce a bonded body and then heat or an active energy ray is allowed to act on the bonded body to dismantle the bonded body, the easily dismantlable bonding material comprising a polyrotaxane that has a ring-shaped molecule having an opening, a linear molecule chain penetrating through the opening in the ring-shaped molecule, and capping groups respectively bonded to both ends of the linear molecule chain, in which the ring-shaped molecule has a polymerizable group.

Description

Adhesive material that can be easily dismantled, joined body and dismantling method

The present invention relates to an easy-to-dismantle adhesive technology.

The easily dismantling adhesive material is an adhesive material that has sufficient adhesive strength according to the purpose of use and a property that the adhesive strength can be lowered at an arbitrary timing and easily peeled (dismantled). Demands for easily dismantled adhesive materials are increasing for purposes such as separating and collecting dissimilar materials, repairing or replacing defective parts, and improving productivity by temporary bonding in the manufacturing process.
Regarding the "dismantling mechanism" of the easily dismantling adhesive material, the mechanical strength decrease due to the decomposition of the polymer used as the adhesive, the physical property change due to the polymer reaction, the solid-liquid conversion due to photoisomerization, and the formation of thermally expandable microcapsules. Various studies and proposals have been made on the expansion and deformation of the adhesive layer due to thermal expansion.

Patent Document 1 is cited as a prior art document relating to adhesives containing thermally expandable microcapsules.
Further, Patent Document 2 discloses a copolymer (X) having an alkoxycarbonyloxystyrene structural unit (a) and a glycidyl group-containing (meth)acrylate structural unit (b), and an acid generator (Y). An adhesive composition is described.

From a perspective different from that of the prior art, the present inventor has designed and developed an easily dismantled adhesive material that utilizes changes in physical properties that accompany polymer reactions (Non-Patent Document 1). Non-Patent Document 1 describes an easily dismantleable adhesive material using a polymer having a tertiary-butoxycarbonyl group in its side chain and using a mechanism whereby the adhesive strength is reduced by decomposition of this functional group.

JP 2006-225544 A JP 2015-7189 A

　In order to design an easily dismantled adhesive material, it is necessary to reduce the adhesive strength once developed. In addition, unlike deterioration over time, it is required to be dismantled on demand and in a short period of time. need to leave

The most important point in designing an easy-to-dismantle adhesive material is how to achieve both high adhesive strength and long-term stability during use and easy dismantling that can be easily removed with a weak force. In other words, design points are that the mechanism for dismantling does not hinder the adhesiveness, and that the adhesive strength decreases at any timing. It is often not easy to achieve both of these contradictory properties.

Based on the above, an object of the present invention is to provide an easily dismantleable adhesive material that has both excellent adhesive strength and easy dismantleability.

The inventors have completed the invention provided below and solved the above problems.

According to the invention,
An easily dismantleable adhesive material used for bonding a first structural member and a second structural member to obtain a joined body, and then dismantling the joined body by applying heat or active energy rays. hand,
A polyrotaxane comprising a cyclic molecule forming an opening, a linear molecular chain passing through the opening of the cyclic molecule, and blocking groups attached to both ends of the linear molecular chain,
An easily dismantling adhesive material is provided in which the cyclic molecule has a polymerizable group.

Moreover, according to the present invention,
a first structural member;
a second structural member;
A joined body is provided, which joins the first structural member and the second structural member, and includes the hardened body of the easily dismantleable adhesive material.

Moreover, according to the present invention,
A dismantling method is provided, which includes a dismantling step of dismantling the bonded body by applying heat or active energy rays to the bonded body.

According to the present invention, an easy-to-dismantle adhesive material having both excellent adhesive strength and easy-to-dismantle property is provided.

FIG. 2 is a diagram for explaining polyrotaxane; It is a figure which shows the TG curve obtained by the thermogravimetric analysis.

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.
The drawings are for illustration only and do not limit the invention.

In this specification, the notation "X to Y" in the explanation of the numerical range means X or more and Y or less unless otherwise specified. For example, "1 to 5% by mass" means "1% by mass or more and 5% by mass or less".

In the description of a group (atomic group) in the present specification, a description without indicating whether it is substituted or unsubstituted includes both those having no substituent and those having a substituent. For example, the term “alkyl group” includes not only alkyl groups without substituents (unsubstituted alkyl groups) but also alkyl groups with substituents (substituted alkyl groups).
The notation "(meth)acryl" used herein represents a concept that includes both acryl and methacryl. The same applies to similar notations such as "(meth)acrylate".
The term "organic group" as used herein means an atomic group obtained by removing one or more hydrogen atoms from an organic compound, unless otherwise specified. For example, a "monovalent organic group" represents an atomic group obtained by removing one hydrogen atom from an arbitrary organic compound.

<Easy disassembly adhesive material>
The easily dismantling adhesive material of the present embodiment adheres a first structural member and a second structural member to obtain a joined body, and then disassembles the joined body by applying heat or active energy rays. used for purposes.
The easily dismantling adhesive material of the present embodiment comprises a cyclic molecule forming an opening, a linear molecular chain penetrating the opening of the cyclic molecule, and blocking groups bonded to both ends of the linear molecular chain. including polyrotaxanes. And the cyclic molecule in this polyrotaxane has a polymerizable group.

Below, the description of the components that the easily dismantleable adhesive material of the present embodiment can contain will be continued.

(Polyrotaxane)
The easily dismantleable adhesive material of the present embodiment contains polyrotaxane.
A polyrotaxane usually comprises a cyclic molecule forming an opening, a linear molecular chain passing through the opening of the cyclic molecule, and blocking groups attached to both ends of the linear molecular chain. Blocking groups prevent the cyclic molecule from leaving the linear chain. A single linear molecular chain can pass through an opening in one or more cyclic molecules.

FIG. 1 is a diagram schematically showing an example of polyrotaxane. The polyrotaxane in FIG. 1 is a cyclic molecule cyclodextrin, a polyether chain (polyoxyethylene chain) which is a linear molecular chain penetrating the opening of the cyclodextrin, and both ends of the polyether chain. and an adamantyl group, which is a blocking group. The bulky adamantyl group prevents the cyclodextrin from leaving the polyether chain.
In this embodiment, a cyclic molecule such as cyclodextrin has a polymerizable group. Specifically, a polymerizable group such as a (meth)acryloyl group is bonded directly or via a linking group to a cyclic molecule such as cyclodextrin.
Although one polyether chain passes through only one cyclodextrin opening in FIG. 1, one polyether chain may pass through two or more cyclodextrin openings.
In FIG. 1, m and n are each independently an integer of 0 or more, preferably 0 or 1 or more, more preferably 1-30, still more preferably 5-15. In addition, x represents the number of repeating ether units constituting the linear molecular chain, and x is, for example, 100 to 5,000, preferably 100 to 3,000, more preferably 100 to 1,000.

The cyclic molecule in the polyrotaxane is not particularly limited as long as it forms an opening through which a linear molecular chain can pass. A cyclic molecule does not have to be completely closed by a covalent bond, as long as the linear molecular chain passing through the opening does not break off.
Cyclic molecules include, for example, cyclodextrins, crown ethers, benzocrowns, dibenzocrowns, dicyclohexanocrowns, and derivatives or modifications thereof. From the viewpoint of inclusion ability of linear molecular chains, the cyclic molecule is preferably cyclodextrin or a derivative or modified form thereof. The cyclodextrins may be of α-type, β-type, or γ-type.
When the cyclic molecule is cyclodextrin or a derivative or modification thereof, some or all of the hydroxy groups in the cyclodextrin may be substituted with any group.
When the cyclic molecule is penetrated by the linear molecular chain, the relative amount of the cyclic molecule to be included (molar ratio ) is, for example, 0.001 or more, preferably 0.01 or more, more preferably 0.1 or more, and the upper limit is, for example, 0.7 or less, preferably 0.6 or less, more preferably 0 .5 or less. When the inclusion amount of the cyclic molecule is within the above range, the mobility of the cyclic molecule on the linear molecular chain is likely to be maintained.

The linear molecular chain in the polyrotaxane is not particularly limited as long as it is a molecular chain that can penetrate the cyclic molecule and the cyclic molecule can move on the linear molecular chain. The straight-chain molecular chain only needs to contain a substantially straight-chain portion, and may have a branched chain or a cyclic substituent or the like. The length and molecular weight of the linear portion are not particularly limited.
Linear molecular chains include, for example, alkylene chains, polyester chains, polyether chains, polyamide chains, and polyacrylate chains. Among these, a polyester chain or a polyether chain is preferred, and a polyether chain is more preferred, from the viewpoint of the flexibility of the linear molecular chain itself. Polyether chains are preferably polyethylene glycol chains (polyoxyethylene chains).

The blocking groups in the polyrotaxane are not particularly limited as long as they are groups arranged at both ends of the linear molecular chain and capable of maintaining the state in which the linear molecular chain penetrates the cyclic molecule.
The blocking group includes a group having a structure larger than the opening of the cyclic molecule, a group that cannot pass through the opening of the cyclic molecule due to ionic interaction, and the like. Specific examples of blocking groups include adamantyl groups, groups containing cyclodextrin, anthracene groups, triphenylene groups, pyrene groups, trityl groups, and isomers and derivatives thereof.

In the polyrotaxane, the combination of a cyclic molecule and a linear molecular chain is preferably a combination of α-cyclodextrin or a derivative thereof as the cyclic molecule and a polyethylene glycol chain or derivative thereof as the linear molecular chain. . This combination facilitates movement of the cyclic molecule on the linear molecular chain. This combination also has the advantage of being relatively easy to synthesize.

As described above, in this embodiment, the cyclic molecule in the polyrotaxane has a polymerizable group. By polymerizing the polymerizable groups, the easily dismantleable adhesive material is cured and develops adhesiveness. In addition, since the cyclic molecule has a polymerizable group, the cyclic molecule can be kept slidable along the linear molecular chain even after heat curing. This contributes to high toughness of the cured product of the easily dismantleable adhesive material.
The polymerizable group may be directly bonded to a cyclic molecule such as cyclodextrin, or may be bonded to a cyclic molecule such as cyclodextrin via some linking group.

The type of the polymerizable group is not particularly limited as long as it exhibits adhesiveness and easy dismantling properties, but from the viewpoint of good adhesiveness, easy dismantling property, stability at room temperature, etc., a preferred polymerizable group is polymerizable carbon. - groups containing carbon double bonds can be mentioned.
The group containing a polymerizable carbon-carbon double bond is preferably a (meth)acryloyl group or a vinyl group, more preferably a (meth)acryloyl group.
In addition, cationic polymerizable groups such as an epoxy group and an oxetanyl group can also be mentioned as the polymerizable group.

A preferred embodiment is an embodiment in which the cyclic molecule is cyclodextrin and the polymerizable group is bonded to the cyclodextrin directly or via a linking group.
A particularly preferred embodiment is one in which the cyclic molecule is cyclodextrin, and at least part of the hydrogen atoms of the hydroxy groups of the cyclodextrin are substituted with groups represented by general formula (I) below. .

In general formula (I),
R is a hydrogen atom or a methyl group,
A is a single bond, -COO- or -CONH-,
B is a single bond or a linear or branched alkylene group,
L is a single bond or a carbonyl group,
p is an integer from 0 to 10,
q is an integer of 0 or more.

A is preferably -CONH-.
B is preferably a linear alkylene group. The carbon number of B is preferably 1-6, more preferably 1-4.
L is preferably a carbonyl group.
p is preferably an integer of 1 to 8, more preferably 4 to 6, still more preferably 5 to 6, and particularly preferably 5. However, when L is a single bond, p is preferably 2-4, more preferably 2-3.
q is preferably an integer of 0 or 1 or more, more preferably 1-30, still more preferably 5-15.

The cyclic molecule may have only one polymerizable group, or may have a plurality of polymerizable groups. When the cyclic molecule has multiple polymerizable groups, the chemical structures of the multiple polymerizable groups may be the same or different.

The weight-average molecular weight of the polyrotaxane is, for example, from 10,000 to 1,000,000, preferably from 100,000 to 1,000,000, from the viewpoint of appropriate applicability (viscosity), strength as an adhesive material, and durability. , more preferably 200,000 to 800,000.

The polyrotaxane may be synthesized with reference to a known method, or may be a commercially available product. Commercially available products include the "Serum" (registered trademark, SeRM in the alphabet) series sold by Advanced Soft Materials Co., Ltd.
Further, for obtaining/synthesizing the polyrotaxane, reference can be made to the description of Examples in Japanese Patent Publication No. 2015-521210. It should be noted that this patent document relates to photocurable coating compositions and coating films, not to easily dismantled adhesive materials.

The easily dismantleable adhesive material of the present embodiment may contain only one type of polyrotaxane, or may contain two or more types.

By the way, since the easily dismantleable adhesive material of the present embodiment contains polyrotaxane, the stress in the cured product of the easily dismantleable adhesive material is relaxed, the cured product can be self-repaired even if it is deformed by an external force, and the adhesive material is resistant to stress. There is a tendency to easily obtain at least one of the effects of increasing the impact resistance.

(Polymerizable carbon-compound having a carbon double bond)
The easily dismantleable adhesive material of the present embodiment may contain a compound having a polymerizable carbon-carbon double bond, which is different from polyrotaxane. The use of such compounds tends to increase the bond strength, especially before the dismantling process.

Examples of compounds having a polymerizable carbon-carbon double bond include monofunctional (meth)acrylates and/or polyfunctional (meth)acrylates. The number of (meth)acryloyl groups per molecule of polyfunctional (meth)acrylate is, for example, 2-8, preferably 2-6, more preferably 2-4.

Specific examples of monofunctional (meth)acrylates include methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, ) alkyl (meth)acrylates such as acrylate, t-butyl (meth)acrylate, n-octyl (meth)acrylate, isooctyl (meth)acrylate, lauryl (meth)acrylate, 2-ethylhexyl (meth)acrylate;
hydroxy group-containing acrylates such as hydroxyethyl acrylate and 4-hydroxybutyl acrylate;
benzyl acrylates such as benzyl (meth)acrylate;
Phenoxy group-containing acrylates such as phenoxyethyl acrylate and phenoxymethyl acrylate;
polyalkylene glycol mono(meth)acrylates such as polyethylene glycol mono(meth)acrylate, polypropylene glycol mono(meth)acrylate, methoxylated polyethylene glycol mono(meth)acrylate; and the like.

Specific examples of polyfunctional (meth)acrylates include ethylene glycol di(meth)acrylate, diethylene glycol di(meth)acrylate, triethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate. ) acrylate, dipropylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, polypropylene glycol di(meth)acrylate, 1,4-butanediol di(meth)acrylate, 1,6-hexanediol di(meth) ) acrylate, 1,9-nonanediol di(meth)acrylate, 1,10-decanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, dimethylol-tricyclodecane di(meth)acrylate, ethylene oxide modified Diacrylate, propylene oxide-modified diacrylate, EO adduct di(meth)acrylate of bisphenol A, EO adduct di(meth)acrylate of hydrogenated bisphenol A, PO adduct di(meth)acrylate of bisphenol A, 1,2 , 3-propanetriol 1,3-dimethacrylate, neopentyl glycol hydroxypivalate di(meth)acrylate, polytetramethylene glycol di(meth)acrylate, polyester diol di(meth)acrylate, polycarbonate diol di(meth)acrylate , polyurethane di(meth)acrylates and other difunctional monomers.

Examples of polyfunctional (meth)acrylates include trimethylolpropane tri(meth)acrylate, EO-modified trimethylolpropane tri(meth)acrylate, PO-modified trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, EO-modified trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, EO-modified pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, ditrimethylolpropane tetra(meth)acrylate, glycerin ethoxy tri (Meth)acrylate, glycerin propoxy tri(meth)acrylate, caprolactone-modified trimethylolpropane tri(meth)acrylate, pentaerythritol ethoxytetra(meth)acrylate, caprolactam-modified dipentaerythritol hexa(meth)acrylate, tris(acryloxyethyl) Trifunctional or higher polyfunctional (meth)acrylates such as isocyanurate and dipentaerythritol pentaacrylate can also be mentioned.

As the compound having a polymerizable carbon-carbon double bond, (meth)acrylate oligomers such as urethane (meth)acrylate oligomers and polyester (meth)acrylates can be used in addition to the above-described monomers.

When using a compound having a polymerizable carbon-carbon double bond, only one type of compound having a polymerizable carbon-carbon double bond may be used, or a plurality of types of compounds having a polymerizable carbon-carbon double bond may be used. may be used.
When using a compound having a polymerizable carbon-carbon double bond, the amount thereof is, for example, 0.1% by mass or more, preferably 0.5% by mass or more, more preferably 1% by mass with respect to 100% by mass of the polyrotaxane. Above, most preferably 5% by mass or more. The upper limit of the amount is, for example, 900% by mass or less, preferably 600% by mass or less, more preferably 300% by mass or less, and most preferably 100% by mass or less with respect to 100% by mass of the polyrotaxane.

(Polymerization initiator)
The easily dismantleable adhesive material of this embodiment may or may not contain a polymerization initiator. The polymerization initiator is not particularly limited as long as it can polymerize the polymerizable group possessed by the cyclic molecule of the polyrotaxane. Polymerization initiators typically generate active chemical species that polymerize the polymerizable groups with heat and/or light (preferably heat).
When using a polymerization initiator, only one polymerization initiator may be used, or two or more polymerization initiators may be used.

Preferred polymerization initiators include azo thermal polymerization initiators and organic peroxide thermal polymerization initiators. Among these, an organic peroxide thermal polymerization initiator is preferable in terms of excellent low-temperature curability.

Specific examples of organic peroxide thermal polymerization initiators include dialkyl peroxides, diacyl peroxides, peroxydicarbonates, peroxyesters, and peroxyketals. More specifically, dialkyl peroxides include t-butyl cumyl peroxide, di-t-butyl peroxide, dicumyl peroxide, di-t-hexyl peroxide and the like. Diacyl peroxides include diisobutyryl peroxide, di(3,5,5-trimethylhexanoyl) peroxide, dilauroyl peroxide, disuccinic acid peroxide, dibenzoyl peroxide, and di(4-methylbenzoyl) peroxide. etc. Examples of peroxydicarbonates include di-n-propylperoxydicarbonate, diisopropylperoxydicarbonate, di-sec-butylperoxydicarbonate, di(2-ethylhexyl)peroxydicarbonate, di(4- t-butylcyclohexyl)peroxydicarbonate and the like. Peroxyesters include t-hexylperoxybenzoate, t-hexylperoxypivalate, 2,5-dimethyl-2,5di(2-ethylhexanoylperoxy)hexane and the like. Peroxyketals include 2,2-bis(4,4-di-t-butylperoxycyclohexyl)propane, 1,1-di(t-hexaperoxy)cyclohexane, 1,1-di(t- butylperoxy)cyclohexane, n-butyl 4,4-(di-butylperoxy)pentanoate, 2,2-di(t-butylperoxy)butane and the like.

Further, as the azo thermal polymerization initiator, for example, 2,2'-azobisisobutyronitrile, 2,2'-azobis (2-methylbutyronitrile), 1,1'-azobis (cyclohexane-1 -carbonitrile), 2,2′-azobis{2-methyl-N-[1,1-bis(hydroxymethyl)ethyl]propionamide}, 2,2′-azobis[2-methyl-N-(2- hydroxyethyl)propionamide], 2,2′-azobis[2-(hydroxymethyl)propionitrile], 2,2′-azobis(2,4-dimethylvaleronitrile), 2,2′-azobis(4-methoxy -2,4-dimethylvaleronitrile), dimethyl 2,2′-azobisisobutyrate, 4,4′-azobis(4-cyanovaleric acid), 2,2′-azobis[2-(2-imidazolin-2-yl ) propane], 2,2′-azobis{2-methyl-N-[1,1-bis(hydroxymethyl)-2-hydroxyethyl]propionamide} and the like.

As one aspect, the easily dismantling adhesive material of the present embodiment preferably contains 1% by mass or more, more preferably 1 to 10% by mass, and still more preferably 1 to 5% by mass of a polymerization initiator in all nonvolatile components. is preferred.
Since the easily dismantleable adhesive material of the present embodiment contains an appropriate amount of polymerization initiator, the polymerizable groups in the polyrotaxane and/or the compound having a polymerizable carbon-carbon double bond are polymerized even at a relatively low temperature. can be made That is, the article can be adhered even by heating at a relatively low temperature.

On the other hand, as another aspect, the easily dismantleable adhesive material of the present embodiment does not contain a polymerization initiator, or even if it contains a polymerization initiator, less than 1% by mass (more preferably less than 0.5% by mass) of the total nonvolatile components It preferably contains an initiator. When the easily dismantleable adhesive material of the present embodiment does not contain a polymerization initiator or contains a small amount of polymerization initiator, it is possible to suppress release of decomposition products of the polymerization initiator as gas. By suppressing gas release, for example, contamination and corrosion of structural members can be suppressed, and a decrease in adhesive strength can be suppressed. In addition, by suppressing gas emission, it becomes easier to apply to applications that require high cleanliness, such as the field of electronic device manufacturing.
By the way, even if the easily dismantleable adhesive material of the present embodiment does not contain a polymerization initiator, the polymerizable group in the polyrotaxane and/or the compound having a polymerizable carbon-carbon double bond is formed by heating at a sufficiently high temperature. Polymerization causes the easily dismantleable adhesive material to harden.

(other ingredients)
The easily dismantleable adhesive material of the present embodiment may contain a polymer other than polyrotaxane. For example, an epoxy resin may be used in combination to increase adhesive strength.

Moreover, the easily dismantling adhesive material of the present embodiment may contain a volatile organic solvent. By using a volatile organic solvent, it becomes easier to apply the easily dismantled adhesive material to the structural member.
As the volatile organic solvent, those capable of dissolving or dispersing the polyrotaxane and sufficiently volatilizing by a normal adhesion process (coating, heating, etc.) can be mentioned without particular limitation. Specifically, acetone, methyl ethyl ketone (MEK), ketones such as cyclohexanone, ethyl acetate, butyl acetate, cellosolve acetate, propylene glycol monomethyl ether acetate, carbitol acetate and other acetic acid esters, cellosolve, butyl carbitol and other carbines. Tolls, aromatic hydrocarbons such as toluene and xylene, dimethylformamide (DMF), dimethylacetamide, N-methylpyrrolidone and the like can be mentioned.

Among the above, acetone, MEK, ethyl acetate, DMF, etc. are preferable because they have a high solubility for polyrotaxane and tend to volatilize easily during use. A volatile organic solvent may be used individually by 1 type, or may be used in combination of 2 or more type.

When the easily dismantleable adhesive material of the present embodiment contains a volatile organic solvent, the amount thereof is preferably such that the nonvolatile component concentration of the easily dismantleable adhesive material is 10 to 50% by mass. The nonvolatile component concentration is more preferably 10 to 40% by mass, more preferably 10 to 30% by mass.
A moderately large amount of the volatile organic solvent can provide better coatability. On the other hand, if the amount of the organic solvent is not too large, the easily dismantling adhesive material will be prevented from "wetting and spreading too much" and the drying time will be shortened.
Just to make sure, the easily dismantleable adhesive material of this embodiment does not need to contain an organic solvent as long as it is possible to bond structural members.

In addition, the easily dismantleable adhesive material of this embodiment may or may not contain various optional components. Examples of optional components include inorganic particles such as silica and alumina, fiber fillers such as glass fiber and carbon fiber, thermoplastic elastomers, flame retardants, antifoaming agents, and silane coupling agents.

(Physical properties of easily dismantled adhesive material)
In the easily dismantleable adhesive material of the present embodiment, the ratio of F2 to F1 (F2/F1) measured under the following conditions is preferably 0.9 or less, more preferably 0.8 or less. The lower limit is not particularly limited and may be 0. For example, 0.01 or more, or 0.1 or more is sufficient. By doing so, it is possible to achieve both high adhesive strength at the time of use and dismantling properties such as easy peeling with a weak force at a high level.
[conditions]
(i) A sample obtained by bonding two stainless steel plates (SUS304) together with an easily dismantling adhesive material is measured for shear bond strength in accordance with JIS K 6850:1999.
(ii) F1 is the shear bond strength of Sample 1 obtained by heat-treating the easily dismantleable adhesive material under the first heat treatment conditions of 150° C. for 7 hours, and after the easily dismantleable adhesive material is heat-treated under the first heat treatment conditions. , and 200° C. for 2 hours.

The technical significance of the F2/F1 value is as follows. The value of F2/F1 indicates ease of dismantling by heating. F2/F1 being less than 1 means that the heat treatment under the second heat treatment conditions reduces the tensile shear bond strength. In an adhesive material using a thermosetting resin, heat treatment at a high temperature generally promotes cross-linking of the thermosetting resin and improves the shear adhesive strength of the cured product. On the other hand, the easily dismantleable adhesive material of the present embodiment has a reduced tensile shear bond strength due to the heat treatment under the second heat treatment conditions. The value of F2/F1 indicates the degree of this decrease, and this value is an index showing the ease of dismantling by heating.

By the way, from the viewpoint of reducing the influence of measurement error/variation, when obtaining F1, it is preferable to perform at least three measurements and adopt the average value of the obtained three or more values as F1. The same is true for F2.

Moreover, from the viewpoint of obtaining stable measured values, it is preferable to sufficiently dry the easily dismantling adhesive material adhered to the stainless steel plate before the heat treatment under the first heat treatment conditions. Drying conditions can be, for example, about overnight (about 8 to 16 hours) under reduced pressure conditions of 50° C. and 10 to 100 Pa.
The sample may also be dried after the heat treatment under the first heat treatment conditions (after curing). The drying conditions here can be, for example, room temperature under reduced pressure conditions of 10 to 100 Pa for about 15 to 20 hours (17.5 hours as a specific example). Alternatively, after the heat treatment under the first heat treatment conditions (after curing), the sample is allowed to stand at room temperature and normal pressure for about 15 to 20 hours (17.5 hours as a specific example) to allow the sample to settle. good too.

From a viewpoint different from ease of dismantling, the cured product of the easily dismantleable adhesive material of the present embodiment tends to be less likely to decrease in adhesive strength when placed at a low temperature or high temperature and then returned to room temperature. . This means that the easily dismantleable adhesive material of this embodiment can be preferably applied, for example, in the manufacture of automobiles.

Specifically, the ratio of F2′ and F1′ (F2′/F1′, index of cold resistance) measured under the following conditions is preferably 0.6 or more, more preferably 0.7 or more, and even more preferably is greater than or equal to 0.8.
[conditions]
(a) A sample obtained by bonding two stainless steel plates (SUS304) together with an easily dismantling adhesive material is measured for shear bond strength in accordance with JIS K 6850:1999.
(b) F1′ is the shear bond strength of Sample 1′ obtained by heat-treating the easily dismantleable adhesive material under the first heat treatment conditions of 150° C. for 7 hours, and the easily dismantleable adhesive material is heat-treated under the first heat treatment conditions. After cooling at -30°C for 2 hours, the shear adhesive strength of sample 2' obtained is defined as F2'.

Just to be sure, F1' is basically synonymous with F1.

In addition, the ratio of F2'' and F1'' measured under the following conditions (F2''/F1'', index of heat resistance) is preferably 0.6 or more, more preferably 0.7 or more, and Preferably it is 0.8 or more.
[conditions]
(a) A sample obtained by bonding two stainless steel plates (SUS304) together with an easily dismantling adhesive material is measured for shear bond strength in accordance with JIS K 6850:1999.
(b) F1'' is the shear bond strength of the sample 1'' obtained by heat-treating the easily dismantleable adhesive material under the first heat treatment conditions of 150°C for 7 hours, and the easily dismantleable adhesive material is treated under the first heat treatment conditions. After the heat treatment, the shear bond strength of sample 2'' obtained by heating at 150° C. for 2 hours is defined as F2''.

Just to be sure, F1'' is basically synonymous with F1.

From a different point of view, it is preferable that the easily dismantleable adhesive material or its cured product have good "thermal stability". Quantitatively, it is as follows.
The 0.5% decomposition temperature of the easily detachable adhesive material (uncured) in thermogravimetric analysis is, for example, 200 to 220°C, preferably 210 to 220°C. Further, the 1% decomposition temperature of the easily dismantling adhesive material (uncured) is, for example, 230 to 260.degree. C., preferably 240 to 260.degree.
The 0.5% decomposition temperature is, for example, 230 to 260.degree. C., preferably 230 to 250.degree. In addition, the 1% decomposition temperature of the cured product obtained by thermogravimetric analysis is, for example, 250 to 280°C, preferably 250 to 270°C.
For details of the conditions for thermogravimetric analysis, refer to the examples given later.

<Dismantling method and articles>
The easily dismantleable adhesive material of the present embodiment can preferably be used in the following processes (1) and (2).
(1) A dismantling adhesive material is sandwiched between a first structural member and a second structural member, and the dismantling adhesive material is heat cured by a first heat treatment. As a result, an article is obtained that includes the first structural member, the second structural member, and the cured adhesive material that bonds the first structural member and the second structural member.
(2) The article obtained in (1) above is subjected to a second heat treatment to dismantle the first structural member and the second structural member.

If the temperature condition adopted for heat curing (first heat treatment) is the first temperature condition, and the temperature condition adopted for disassembly (second heat treatment) is the second temperature condition, then the second temperature condition is the first temperature condition. A higher temperature is preferable.

The materials and properties of the first structural member and the second structural member are not particularly limited. Examples of materials include metals such as aluminum, aluminum alloys, and SUS, plastics such as polypropylene, polyethylene, and nylon, and ceramics. In this embodiment, both the first structural member and the second structural member are preferably metallic structural members.
The structural member may be subjected to various surface treatments, or may not be subjected to surface treatment. In terms of adhesive strength and ease of dismantling, it is preferable to remove foreign matter/contamination by cleaning the surface of the structural member before applying the easy-to-dismantle adhesive to the surface of the structural member. .
Incidentally, from the viewpoint of good adhesiveness, durability, etc., it is preferable that one or both of the first structural member and the second structural member are not made of a resin film.
Further, the easily dismantleable adhesive material of the present embodiment is used for bonding a first structural member and a second structural member. Therefore, normally, the cured body of the easily dismantleable adhesive material is sandwiched between the first structural member and the second structural member and is not exposed.

The method of adhering the easily dismantling adhesive material to the surface of the first structural member and/or the second structural member is not particularly limited. If the easily dismantling adhesive material has a viscosity that allows it to be applied, the easily dismantling adhesive material may be applied to the surface of the structural member by a known coating method.

After attaching (applying) the easily dismantling adhesive material to the surface of the structural member, and before heat-curing the easily dismantling adhesive material by the first heat treatment, it is applied under reduced pressure (specifically, 10 to 100 Pa). drying treatment is preferably performed. By performing a sufficient drying treatment, the solvent in the easily dismantleable adhesive material is sufficiently removed, and as a result, it is thought that the adhesive strength can be further increased. The drying treatment here may be performed at room temperature (without heating), or may be performed with heating at about 30 to 100°C. The drying time here is, for example, about 3 to 24 hours.
Just to be sure, as long as sufficient adhesive strength and easy disassembly after bonding are exhibited, drying treatment may not be performed, and even if some treatment is performed, the specific conditions are particularly Not limited.

In addition, drying treatment under reduced pressure (specifically, 10 to 100 Pa) may be performed even after heat curing of the easily dismantleable adhesive material. The drying treatment here may be performed with heating at, for example, 30 to 100° C., specifically about 30 to 50° C., but is preferably performed at room temperature (without heating). The drying time here is, for example, about 1 to 24 hours.
Just to be sure, as long as sufficient adhesive strength and easy dismantling after adhesion are exhibited, drying treatment under reduced pressure may not be performed, and even if some treatment is performed, it is specific. conditions are not particularly limited. In some cases, it is sufficient to simply leave the heat-cured easily dismantleable adhesive material at room temperature for about 1 to 24 hours.

When the temperature under the first temperature condition is T1 and the temperature under the second temperature condition is T2, the value of (T2-T1) is preferably 30°C or higher, more preferably 40°C or higher, and even more preferably 50°C or higher. . By doing so, sufficient hardened body strength and dismantling easiness can be achieved.
The upper limit of the value of (T2-T1) is preferably 130.degree.
Practically preferred temperature conditions are T1 of 20 to 160°C and T2 of 170 to 250°C.

The time for the first heat treatment is not particularly limited as long as the easily dismantleable adhesive material is sufficiently hardened. As an example, the duration of the first heat treatment is 1 to 24 hours.
The time for the second heat treatment is not particularly limited as long as the easy dismantling property is exhibited. As an example, the duration of the second heat treatment is 5 minutes to 6 hours.

Incidentally, active energy rays may be applied to the hardened body instead of/along with the second heat treatment as long as the dismantling property is exhibited.

<Examples of easily dismantled adhesive materials>
The easily dismantleable adhesive material can be configured to include, for example, the following (A) and (B).
(A) a cyclic molecule having a polymerizable group and forming an opening, a linear molecular chain passing through the opening of the cyclic molecule, and blocking groups bonded to both ends of the linear molecular chain; Polyrotaxane provided (B) A compound having a polymerizable carbon-carbon double bond, which is different from the above (A)

The polymerizable group in (A) above is preferably a group containing a polymerizable carbon-carbon double bond, and can be, for example, a (meth)acryloyl group. The cyclic molecule in the above (A) is a cyclodextrin, and it is preferable that the polymerizable group is bonded to the cyclodextrin directly or via a linking group. A preferred embodiment of the cyclic molecule is cyclodextrin, and more preferably, at least part of the hydrogen atoms of the hydroxy groups of this cyclodextrin are substituted with groups represented by general formula (I) below.

In general formula (I), R is a hydrogen atom or a methyl group, A is a single bond, -COO- or -CONH-, B is a single bond, or a linear or branched alkylene group, L is a single bond or a carbonyl group, p is an integer of 0 to 10, and q is an integer of 0 or more.

Embodiments of the easily dismantleable adhesive material including the above (A) and (B) include the following.

[Aspect 1]
An easily dismantled adhesive material containing the following (A) and (B1).
Component (A) A rotaxane containing a cyclodextrin and a linear molecular chain penetrating the opening of the cyclodextrin, wherein a (meth)acryloyl group is bound directly or via a linking group to the cyclodextrin. A rotaxane (hereinafter referred to as rotaxane a), wherein the linear molecular chain has blocking groups attached to each end thereof
(B1) Component A monomer having one polymerizable carbon-carbon double bond in the molecule

[Aspect 2]
An easily dismantleable adhesive material containing (A) and (B1) and/or (B2) below.
(A) Component Rotaxane a
(B1) component monomer having one polymerizable carbon-carbon double bond in the molecule (B2) component polyfunctional monomer having two or more polymerizable carbon-carbon double bonds in the molecule

Examples of aspect 1 include the following.
[Example 1-1]
An easily dismantled adhesive material containing the following (A) and (B1).
(A) Rotaxane a
(B1) Alkyl (meth)acrylate such as n-butyl (meth)acrylate, isobutyl (meth)acrylate, n-octyl (meth)acrylate, isooctyl (meth)acrylate, lauryl (meth)acrylate, and 2-ethylhexyl (meth)acrylate meth)acrylate;
hydroxy group-containing acrylates such as hydroxyethyl acrylate and 4-hydroxybutyl acrylate;
benzyl acrylates such as benzyl (meth)acrylate;
Phenoxy group-containing acrylates such as phenoxyethyl acrylate and phenoxymethyl acrylate;
Polyalkylene glycol mono(meth)acrylates such as polyethylene glycol mono(meth)acrylate, polypropylene glycol mono(meth)acrylate, methoxylated polyethylene glycol mono(meth)acrylate;
One or two or more monomers selected from the group consisting of

Examples of aspect 2 include the following.
[Example 2-1]
An easily dismantled adhesive material containing the following (A) and (B2).
(A) Rotaxane a
(B2) triethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, polypropylene glycol di(meth)acrylate, 1,4- butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, dimethylol-tricyclodecane di(meth)acrylate acrylate, ethylene oxide-modified diacrylate, propylene oxide-modified diacrylate, EO adduct di(meth)acrylate of bisphenol A, PO adduct di(meth)acrylate of bisphenol A, neopentyl glycol hydroxypivalate di(meth)acrylate, Bifunctional monomers such as polytetramethylene glycol di(meth)acrylate, polyester diol di(meth)acrylate, polycarbonate diol di(meth)acrylate, and polyurethane di(meth)acrylate:
Trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, EO-modified trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, EO-modified pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa (meth)acrylate, ditrimethylolpropane tetra(meth)acrylate, glycerin propoxy tri(meth)acrylate, caprolactone-modified trimethylolpropane tri(meth)acrylate, pentaerythritol ethoxytetra(meth)acrylate, caprolactam-modified dipentaerythritol hexa(meth)acrylate ) Trifunctional or higher polyfunctional (meth)acrylates such as acrylates;
One or two or more monomers selected from the group consisting of

[Example 2-2]
An easily dismantleable adhesive material containing the following (A) and one or both of (B1) and (B2).
(A) Rotaxane a
(B1) Alkyl (meth)acrylate such as n-butyl (meth)acrylate, isobutyl (meth)acrylate, n-octyl (meth)acrylate, isooctyl (meth)acrylate, lauryl (meth)acrylate, and 2-ethylhexyl (meth)acrylate meth)acrylate;
hydroxy group-containing acrylates such as hydroxyethyl acrylate and 4-hydroxybutyl acrylate;
benzyl acrylates such as benzyl (meth)acrylate;
Phenoxy group-containing acrylates such as phenoxyethyl acrylate and phenoxymethyl acrylate;
Polyalkylene glycol mono(meth)acrylates such as polyethylene glycol mono(meth)acrylate, polypropylene glycol mono(meth)acrylate, methoxylated polyethylene glycol mono(meth)acrylate;
One or two or more monomers selected from the group consisting of (B2) triethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate, tripropylene glycol di(meth) ) acrylate, polypropylene glycol di(meth)acrylate, 1,4-butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, neopentyl glycol Di(meth)acrylate, dimethylol-tricyclodecane di(meth)acrylate, ethylene oxide-modified diacrylate, propylene oxide-modified diacrylate, EO adduct di(meth)acrylate of bisphenol A, PO adduct di(meth)acrylate of bisphenol A ) acrylate, neopentylglycol hydroxypivalate di(meth)acrylate, polytetramethylene glycol di(meth)acrylate, polyester diol di(meth)acrylate, polycarbonate diol di(meth)acrylate, polyurethane di(meth)acrylate, etc. Functional monomer:
Trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, EO-modified trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, EO-modified pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa (meth)acrylate, ditrimethylolpropane tetra(meth)acrylate, glycerin propoxy tri(meth)acrylate, caprolactone-modified trimethylolpropane tri(meth)acrylate, pentaerythritol ethoxytetra(meth)acrylate, caprolactam-modified dipentaerythritol hexa(meth)acrylate ) Trifunctional or higher polyfunctional (meth)acrylates such as acrylates;
One or two or more monomers selected from the group consisting of

In each of the above examples, acrylate oligomers and other oligomers may be blended. Moreover, you may mix|blend a polymerization initiator.

[Example 3-1: Formulation example containing a polymerization initiator]
0.25 mL of a solvent such as acetone was added to 30 mg of the polyrotaxane used in Example 1 described later, and further dicumyl peroxide was added to polyrotaxane: dicumyl peroxide = 100: 1 to 1000: 1 (mass ratio).

[Example 3-2: Formulation example containing a polymerization initiator]
0.25 mL of a solvent such as acetone is added to 30 mg of the polyrotaxane used in Example 1 below, and dimethyl 2,2′-azobisisobutyrate is added to polyrotaxane: dimethyl 2,2′-azobisisobutyrate=100. : 1 to 1000:1 (mass ratio).

[Example 4: Example of using polyfunctional acrylate in combination]
0.1 to 0.3 mL of a solvent such as acetone was added to 30 mg of a mixture of polyrotaxane: hyperbranched polymer = 100:5 to 100:100 (mass ratio) used in Example 1 described later. thing. The hyperbranched polymer is synthesized by the method described in Japanese Patent No. 6516319, for example.

Although the embodiments of the present invention have been described above, these are examples of the present invention, and various configurations other than those described above can be adopted. Moreover, the present invention is not limited to the above-described embodiments, and includes modifications, improvements, etc. within the scope of achieving the object of the present invention.

Embodiments of the present invention will be described in detail based on examples and comparative examples. It should be noted that the invention is not limited to the examples only.

<Example 1>
[Preparation of easily dismantled adhesive material]
First, referring to the description in JP-A-2011-46917, a polyrotaxane having a total molecular weight of 400,000 g/mol and a linear molecular chain portion molecular weight of 20,000 g/mol was synthesized. This polyrotaxane, as shown in FIG. 1, comprises a polyether chain passing through openings in a cyclic molecule, cyclodextrin, and adamantyl groups bonded to both ends of the polyether chain. In addition, at least part of the hydrogen atoms of the hydroxy group of the cyclodextrin is substituted by the group represented by the general formula (I) (R is a methyl group, A is -CONH-, B is -CH ₂ CH ₂ —, L is a carbonyl group, p is 5, and q is about 8 to 10).
30 mg of this polyrotaxane was dissolved in 0.25 mL of acetone to prepare an easily dismantleable adhesive material that could be applied.

[Measurement of thermal properties]
The easily dismantleable adhesive material itself and the cured product obtained by heating and curing the easily dismantleable adhesive material at 150° C. for 7 hours, 10 hours or 16 hours are each subjected to thermogravimetric analysis to obtain a TG curve. Painted. The conditions for thermogravimetric analysis are as follows.
・Measurement start temperature: room temperature ・Temperature increase rate: 10°C/min ・Atmosphere: nitrogen gas

The 0.5% decomposition temperature and the 1% decomposition temperature were obtained from the TG curve of the cured product obtained by curing the easily dismantling adhesive material at 150° C. for 7 hours. Table 1 shows the results.
For reference, the TG curve itself is shown in FIG.

[Preparation of conjugate]
A conjugate for evaluation was produced in the following manner.
(1) Application of Easily Dismantled Adhesive Material to First Structural Member A stainless steel plate (SUS304) was prepared as the first structural member. 25 μL of the prepared easily dismantling adhesive material was applied to a 1 cm×1 cm area on the surface of this stainless steel plate and dried overnight under reduced pressure conditions of 50° C. and 10 to 100 Pa.
(2) Application of Easily Dismantled Adhesive Material to Second Structural Member As the second structural member, a stainless steel plate (SUS304) different from (1) above was prepared. This stainless steel plate was coated with the easily dismantled adhesive material prepared in the same manner and under the same conditions as in (1) above, and dried.
(3) Adhesion The two stainless steel plates prepared in (1) and (2) above were laminated together by overlapping the 1 cm×1 cm regions coated with the easily dismantling adhesive material. After that, it was heated at 150° C. for 7 hours to cure the easily dismantling adhesive material. After that, it was allowed to stand at room temperature under reduced pressure conditions of 10 to 100 Pa for 17.5 hours.
As described above, a joined body in which two stainless steel plates were joined was obtained.

[Evaluation of shear bond strength]
The shear bond strength of the bonded body obtained in the above [Production of bonded body] was measured in accordance with JIS K 6850:1999 at room temperature (23° C.) and a test speed of 1 mm/min.
The measurement was performed 3 times and the average value was taken as F1.

[Evaluation of easy disassembly]
First, the bonded body obtained in the above [Fabrication of bonded body] was heated at 200° C. for 2 hours (dismantling treatment). Then, it was allowed to stand (to cool) at room temperature for 30 minutes.
After that, the shear bond strength of the joined body was measured under the same conditions as in [Evaluation of Shear Bond Strength] above.
The measurement was performed 3 times, and the average value was taken as F2.

The results are shown in Table 2.

As shown in Table 2, when a cured adhesive material containing a specific polyrotaxane was heated, it exhibited easy disassembly.

[Evaluation of cold resistance]
The bonded body obtained as described in [Preparation of bonded body] above was cooled at −30° C. for 2 hours, then returned to room temperature, and then subjected to [Evaluation of shear bond strength]. , and the shear adhesive strength F2' (average value of three times) was obtained.
Moreover, 2.48 MPa, which is the value of F1, was adopted as the shear bond strength F1′ (average value of three times).

The results are shown in Table 3.

As shown in Table 3, the decrease in adhesive strength due to cooling was suppressed.

[Evaluation of heat resistance]
The bonded body obtained as described in [Preparation of bonded body] above was heated at 150° C. for 2 hours, then returned to room temperature, and as described in [Evaluation of shear bond strength], A shear bond strength F2'' (average of 9 times) was obtained.
Moreover, 2.48 MPa, which is the value of F1, was adopted as the shear adhesive strength F1″ (average value of three times).

The results are shown in Table 4.

As shown in Table 4, the adhesive strength did not decrease even with heating (heating at a temperature lower than the dismantling temperature).

<Example 2>
The same polyrotaxane as used in Example 1 and commercially available trimethylolpropane trimethacrylate (TTMA) were mixed at polyrotaxane/TTMA=9/1 (w/w) to obtain a mixture. 30 mg of this mixture was dissolved in 0.25 mL of acetone to prepare a coatable, easily dismantled adhesive material.

Using the prepared easily dismantling adhesive material, almost the same as in Example 1, production of a joined body, evaluation of shear adhesive strength (measurement of F1), and evaluation of easy dismantling (measurement of F2) were performed. However, in order to increase the reliability of the numerical value, the average value of nine measurements was used for F1.

The results are shown in Table 5.

As shown in Table 5, the cured product of the adhesive material of Example 2, in which the specific polyrotaxane and the compound having a polymerizable carbon-carbon double bond were used in combination, also showed easy disassembly.
In particular, in Example 2, F1, that is, the shear bond strength before dismantling treatment was significantly higher than in Example 1, while the magnitude of F2 was about the same as in Example 1. That is, the adhesive material of Example 2 can bond the structural members together more strongly than the adhesive material of Example 1, but the force required for dismantling is the same for the adhesive material of Example 1 and the adhesive material of Example 2. It was about From the viewpoint of increasing the bonding strength before dismantling treatment, it can be said that it is preferable to use a specific polyrotaxane and a compound having a polymerizable carbon-carbon double bond in combination.

This application claims priority based on Japanese Patent Application No. 2021-024069 filed on February 18, 2021, and the entire disclosure thereof is incorporated herein.

Claims

An easily dismantleable adhesive material used for bonding a first structural member and a second structural member to obtain a joined body, and then dismantling the joined body by applying heat or active energy rays. hand,
A polyrotaxane comprising a cyclic molecule forming an opening, a linear molecular chain passing through the opening of the cyclic molecule, and blocking groups attached to both ends of the linear molecular chain,
An easily dismantling adhesive material in which the cyclic molecule has a polymerizable group.
The easily dismantleable adhesive material according to claim 1,
The easily dismantling adhesive material, wherein the polymerizable group is a group containing a polymerizable carbon-carbon double bond.
The easily dismantleable adhesive material according to claim 1 or 2,
The easily dismantling adhesive material, wherein the polymerizable group is a (meth)acryloyl group.
The easily dismantleable adhesive material according to any one of claims 1 to 3,
The easily dismantling adhesive material, wherein the cyclic molecule is cyclodextrin, and the polymerizable group is bonded to the cyclodextrin directly or via a linking group.
The easily dismantleable adhesive material according to any one of claims 1 to 4,
The easily dismantling adhesive material, wherein the cyclic molecule is cyclodextrin, and at least part of the hydrogen atoms of the hydroxy groups of the cyclodextrin are substituted with groups represented by general formula (I) below.

In general formula (I),
R is a hydrogen atom or a methyl group,
A is a single bond, -COO- or -CONH-,
B is a single bond or a linear or branched alkylene group,
L is a single bond or a carbonyl group,
p is an integer from 0 to 10,
q is an integer of 0 or more.
The easily dismantleable adhesive material according to any one of claims 1 to 5,
An easily dismantling adhesive material containing a compound having a polymerizable carbon-carbon double bond, which is different from the polyrotaxane.
The easily dismantleable adhesive material according to any one of claims 1 to 6,
An easily dismantleable adhesive material containing less than 1% by mass of a polymerization initiator in all non-volatile components.
The easily dismantleable adhesive material according to any one of claims 1 to 7,
contains volatile organic solvents,
An easily dismantleable adhesive material having a non-volatile component concentration of 10 to 50% by mass.
The easily dismantleable adhesive material according to any one of claims 1 to 8,
The easily dismantleable adhesive material is sandwiched between a first structural member and a second structural member, and a first heat treatment is performed to obtain an article in which the first structural member and the second structural member are adhered. an easy-to-dismantle adhesive material used for dismantling the first structural member and the second structural member by subjecting the article to a second heat treatment thereafter.
The easily dismantleable adhesive material according to any one of claims 1 to 9,
An easily dismantling adhesive material having a ratio of F1 to F2 (F2/F1) measured under the following conditions of 0.9 or less.
[conditions]
(i) For a sample in which two stainless steel plates (SUS304) are adhered with the easily dismantleable adhesive material, the shear adhesive strength is measured according to JIS K 6850:1999.
(ii) F1 is the shear bond strength of Sample 1 obtained by heat-treating the easily dismantleable adhesive material under the first heat treatment conditions of 150° C. for 7 hours, and the easily dismantleable adhesive material is heat-treated under the first heat treatment conditions. After that, the shear adhesive strength of Sample 2 obtained by heat treatment under the second heat treatment conditions of 200° C. for 2 hours is defined as F2.
The easily dismantleable adhesive material according to any one of claims 1 to 10,
An easily dismantling adhesive material having a ratio of F1' to F2'(F2'/F1') measured under the following conditions of 0.6 or more.
[conditions]
(a) For a sample in which two stainless steel plates (SUS304) are adhered with the easily dismantleable adhesive material, the shear adhesive strength is measured according to JIS K 6850:1999.
(b) F1′ is the shear bond strength of the sample 1′ obtained by heat-treating the easily dismantleable adhesive material under the first heat treatment conditions of 150° C. for 7 hours; F2' is the shear bond strength of sample 2' obtained by cooling at -30°C for 2 hours after the heat treatment.
a first structural member;
a second structural member;
A joined body comprising the cured body of the easily dismantleable adhesive material according to any one of claims 1 to 11, which joins the first structural member and the second structural member.
A conjugate according to claim 12, wherein
The first structural member and the second structural member are both structural members made of metal.
A dismantling method, comprising a dismantling step of dismantling the joined body according to claim 12 or 13 by applying heat or active energy rays to the joined body.
The dismantling method according to claim 14,
The dismantling method, wherein the dismantling step includes a step of applying heat of 170 to 250° C. to the joined body.