Vibration-damping laminate

Abstract

The present invention pertains to a damping laminate that includes: a thermoplastic elastomer sheet formed by including a thermoplastic elastomer (a) that includes at least one copolymer block (A) with a glass transition temperature of 30°C or less, and having a plurality of through holes; and a fiber-reinforced resin layer disposed on one surface or both surfaces of the thermoplastic elastomer sheet.

Description

[Technical Field]

[0001] The present invention relates to a vibration-damping laminate. [Background technology]

[0002] BACKGROUND ART A composite substrate using a reinforcing fiber fabric and a hydrogenated product of a block copolymer of a vinyl aromatic compound and a conjugated diene compound (Patent Document 1) has been known. Also known is a prepreg (Patent Document 2) that includes a carbon fiber reinforced resin layer and a nonwoven fabric made of a thermoplastic elastomer or polyolefin. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Patent Publication No. 2015-193751 [Patent Document 2] International Publication No. 2012 / 011487 Summary of the Invention [Problem to be solved by the invention]

[0004] However, there are cases where the composite substrate described in Patent Document 1 is required to have even greater rigidity and vibration-damping properties. Furthermore, according to the investigations of the present inventors, the prepreg described in Patent Document 2 does not have sufficient vibration-damping properties.

[0005] The problem to be solved by the present invention is to provide a vibration-damping laminate that has excellent interlayer adhesion and excellent rigidity, and also has extremely excellent vibration-damping properties. [Means for solving the problem]

[0006] As a result of extensive research, the present inventors have discovered that the above problems can be solved by a laminate including a fiber-reinforced resin layer on one or both sides of a specific thermoplastic elastomer sheet, and have arrived at the present invention. That is, the present invention includes the following preferred embodiments. [1] A thermoplastic elastomer sheet comprising a thermoplastic elastomer (a) containing at least one copolymer block (A) having a glass transition temperature of 30°C or less, and having a plurality of through-holes; a fiber-reinforced resin layer disposed on one or both sides of the thermoplastic elastomer sheet; A vibration-damping laminate comprising: [2] The vibration-damping laminate according to [1], wherein the thermoplastic elastomer (a) contains at least one copolymer block (B) containing structural units derived from one or more compounds selected from the group consisting of vinyl aromatic compounds, olefin compounds, urethane compounds, and ester compounds. [3] The vibration-damping laminate according to [1] or [2], wherein the thermoplastic elastomer (a) is a block copolymer comprising at least one copolymer block (A) comprising structural units derived from a conjugated diene compound and at least two copolymer blocks (B) comprising structural units derived from a vinyl aromatic compound, and / or a hydrogenated product of the block copolymer. [4] The vibration-damping laminate according to any one of [1] to [3], wherein the thermoplastic elastomer (a) has a weight-average molecular weight of 40,000 or more and 500,000 or less. [5] In the thermoplastic elastomer sheet, for 100 parts by mass of the thermoplastic elastomer (a), The content of the hydrocarbon-based softener (b) is 10 parts by mass or more and 300 parts by mass or less, The content of the polyolefin resin (c) is 50 parts by mass or less. The vibration-damping laminate according to any one of the above [1] to [4]. [6] In the thermoplastic elastomer sheet, for 100 parts by mass of the thermoplastic elastomer (a), The content of the hydrocarbon-based softener (b) is 10 parts by mass or more and 300 parts by mass or less, The content of the polyolefin resin (c) is 2 parts by mass or more and 50 parts by mass or less. The vibration-damping laminate according to any one of the above [1] to [5]. [7] The vibration-damping laminate according to any one of [1] to [6], wherein the thermoplastic elastomer sheet has an opening ratio of 5% or more and 80% or less. [8] The vibration-damping laminate according to any one of [1] to [7], wherein the thermoplastic elastomer sheet has an average through-hole diameter of 50 μm or more and 6000 μm or less. [9] The thermoplastic elastomer sheet is 1 piece / cm 2 More than 80 pieces / cm 2 The vibration-damping laminate according to any one of the above [1] to [8], which has the following through-hole density:

[10] The vibration-damping laminate according to any one of [1] to [9], wherein the fiber-reinforced resin layer contains one or more types of fibers selected from the group consisting of carbon fibers, silica fibers, glass fibers, aramid fibers, boron fibers, alumina fibers, and silicon carbide fibers. [Effects of the Invention]

[0007] According to the present invention, it is possible to provide a vibration-damping laminate that has excellent interlayer adhesion and rigidity, and also has extremely excellent vibration-damping properties. DETAILED DESCRIPTION OF THE INVENTION

[0008] The vibration-damping laminate of the present invention comprises a thermoplastic elastomer sheet having a plurality of through-holes (hereinafter also referred to as a "perforated sheet"), and a fiber-reinforced resin layer disposed on one or both sides of the sheet. In one embodiment of the present invention, the vibration-damping laminate comprises a perforated sheet and a fiber-reinforced resin layer disposed on one or both sides of the sheet.

[0009] [Perforated sheet] The perforated sheet comprises (a) a thermoplastic elastomer, (b) a hydrocarbon-based softener, optionally (c) a polyolefin-based resin, and optionally (d) an additive.

[0010] <(a) Thermoplastic elastomer> The thermoplastic elastomer (a) contained in the porous sheet of the present invention contains at least one copolymer block (A) having a glass transition temperature of not more than 30° C. In the present invention, the glass transition temperature refers to the glass transition temperature measured by differential scanning calorimetry (DSC), and the measurement method is as described in the Examples below.

[0011] The thermoplastic elastomer (a) contained in the porous sheet may be a single type or a combination of two or more types differing in, for example, the type or content of copolymer blocks, weight average molecular weight and / or hydrogenation rate.

[0012] The glass transition temperature of the copolymer block (A) is preferably 27°C or lower, more preferably 25°C or lower, and preferably -45°C or higher, more preferably -42°C or higher, and even more preferably -40°C or higher. The glass transition temperature of the copolymer block (A) can be adjusted to a desired range, for example, by selecting the stereoregularity of the copolymer block (A). The glass transition temperature of the copolymer block (A) can be measured by the method described in the Examples.

[0013] The thermoplastic elastomer (a) contains at least one copolymer block (A), and thus has a large loss tangent (hereinafter also referred to as "tan δ") at room temperature, which can impart extremely high vibration-damping properties to the vibration-damping laminate of the present invention. Even if a perforated sheet similar to that of the present invention is produced using a thermoplastic elastomer that does not contain the copolymer block (A), and a laminate similar to that of the present invention is manufactured, it is difficult to solve the problems of the present invention.

[0014] Examples of the copolymer block (A) include blocks containing structural units derived from conjugated diene compounds such as butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 1,3-hexadiene, and chloroprene. The copolymer block (A) is preferably a block consisting of structural units derived from a conjugated diene compound. Examples of blocks containing structural units derived from a conjugated diene compound include homopolymer blocks obtained from one type of conjugated diene compound, random copolymer blocks, block copolymer blocks, and graft copolymer blocks composed of two or more types of conjugated diene compounds, as well as polymer blocks containing the above homopolymer blocks or copolymer blocks in their structures. Among these, the above homopolymer blocks and copolymer blocks are preferred. Furthermore, butadiene, isoprene, and mixtures thereof are preferred as conjugated diene compounds.

[0015] The content of the copolymer block (A) in the thermoplastic elastomer (a) is not particularly limited. From the viewpoint of easily obtaining flexibility and desired vibration-damping properties of the vibration-damping laminate, the content is preferably 40% by mass or more, more preferably 45% by mass or more, even more preferably 50% by mass or more, particularly preferably 60% by mass or more, and is preferably 95% by mass or less, more preferably 90% by mass or less, even more preferably 85% by mass or less, particularly preferably 80% by mass or less, based on the mass of the thermoplastic elastomer (a). The contents of the copolymer block (A) and the copolymer block (B) described later in the thermoplastic elastomer (a) can be determined, for example, by nuclear magnetic resonance spectroscopy ( 1 H-NMR, 13 It can be measured by C-NMR.

[0016] In a preferred embodiment, the thermoplastic elastomer (a) includes at least one copolymer block (B) in addition to the copolymer block (A). Examples of the copolymer block (B) include blocks containing structural units derived from one or more compounds selected from the group consisting of vinyl aromatic compounds, olefinic compounds, urethane compounds, and ester compounds. The copolymer block (B) is preferably a block containing structural units derived from the above compounds. Among these, the copolymer block (B) is preferably a block containing structural units derived from a vinyl aromatic compound.

[0017] Examples of vinyl aromatic compounds include styrene, α-methylstyrene, 1-vinylnaphthalene, 2-vinylnaphthalene, 3-methylstyrene, 4-propylstyrene, 4-cyclohexylstyrene, 4-dodecylstyrene, 2-ethyl-4-benzylstyrene, 4-(phenylbutyl)styrene, etc. One type of vinyl aromatic compound may be used alone, or two or more types may be used in combination. Styrene is most preferred.

[0018] Examples of the olefinic compound include ethylene, propylene, 1-butene, etc. One type of olefinic compound may be used alone, or two or more types may be used in combination. The olefinic compound is preferably ethylene or propylene, and more preferably propylene.

[0019] Examples of urethane compounds include reaction products of aliphatic, alicyclic, araliphatic, or aromatic isocyanates with polyols having a number weight average molecular weight of 400 to 10,000. One type of urethane compound may be used alone, or two or more types may be used in combination. The isocyanate is preferably an aliphatic polyisocyanate, and among these, hexamethylene diisocyanate (HDI) or heptamethylene diisocyanate (PDI) is preferred.

[0020] Examples of the ester compound include ester compounds of aromatic dicarboxylic acids and aliphatic or alicyclic diols. One type of ester compound may be used alone, or two or more types may be used in combination. Preferred ester compounds are butylene naphthalate (ester of 2,6-naphthalenedicarboxylic acid and 1,4 butanediol) and butylene terephthalate (ester of terephthalic acid and 1,4 butanediol), and more preferably butylene terephthalate.

[0021] When the thermoplastic elastomer (a) contains the copolymer block (B), the content of the copolymer block (B) in the thermoplastic elastomer (a) is not particularly limited. From the viewpoint of easily obtaining the flexibility and desired vibration-damping properties of the vibration-damping laminate, the content is preferably 5% by mass or more, more preferably 8% by mass or more, even more preferably 10% by mass or more, particularly preferably 15% by mass or more, and is preferably 60% by mass or less, more preferably 55% by mass or less, even more preferably 50% by mass or less, particularly preferably 45% by mass or less, based on the mass of the thermoplastic elastomer (a).

[0022] From the viewpoints of vibration damping, flexibility, heat resistance, and mechanical properties, the thermoplastic elastomer (a) preferably contains at least one copolymer block (A) and at least two copolymer blocks (B). The bonding mode between the copolymer block (A) and the copolymer block (B) may be linear, branched, or any combination thereof. When the copolymer block (A) is represented by A and the copolymer block (B) is represented by B, the thermoplastic elastomer (a) preferably has a triblock structure represented by BAB, or (AB) n and (BA) n It is preferable that the copolymer has a multi-block structure represented by -B (where n is an integer of 2 or more), and it is more preferable that the copolymer has a tri-block structure, from the viewpoint of easily obtaining heat resistance, mechanical properties, stain resistance, and ease of handling in addition to the desired vibration damping properties.

[0023] In a preferred embodiment, the thermoplastic elastomer (a) is a block copolymer comprising at least one copolymer block (A) comprising structural units derived from a conjugated diene compound and at least two copolymer blocks (B) comprising structural units derived from a vinyl aromatic compound, and / or a hydrogenated product of the block copolymer.

[0024] When the thermoplastic elastomer (a) contains a copolymer block (A) containing structural units derived from isoprene and / or butadiene, the content of 3,4-bond units and 1,2-bond units in the structural units derived from isoprene and / or butadiene (hereinafter also referred to as "vinyl bond content") is preferably 5 mol% or more based on all structural units derived from isoprene and butadiene, from the viewpoint of easily obtaining impact absorption and / or desired vibration damping properties. The vinyl bond content is more preferably 10 mol% or more, even more preferably 15 mol% or more, and usually 80 mol% or less, more preferably 75 mol% or less, even more preferably 70 mol% or less. The vinyl bond content is determined by measuring the content of 3,4-bond units and 1,2-bond units in structural units derived from isoprene and / or butadiene using iodine value measurement, infrared spectrophotometer (IR), nuclear magnetic resonance spectroscopy ( 1 H-NMR, 13 It can be determined from the measured value by measurement using a C-NMR or the like.

[0025] From the viewpoint of heat resistance, light resistance, or weather resistance, the thermoplastic elastomer (a) is preferably such that 50 mol% or more of the carbon-carbon double bonds derived from the conjugated diene compound in the copolymer block (A) are hydrogenated. The hydrogenation rate is more preferably 75 mol% or more, even more preferably 95 mol% or more, and particularly preferably 98 mol% or more, and is usually 100 mol% or less, for example, 99 mol% or less. The hydrogenation rate can be determined by iodine value measurement, infrared spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), or the like. 1 H-NMR, 13 It can be measured by C-NMR etc.

[0026] The weight average molecular weight of the thermoplastic elastomer (a) is preferably 40,000 or more, more preferably 50,000 or more, particularly preferably 70,000 or more, from the viewpoint of easily obtaining moldability, flexibility, and mechanical properties of the porous sheet, and is preferably 500,000 or less, more preferably 400,000 or less, particularly preferably 350,000 or less. In the present invention, the weight average molecular weight means the weight average molecular weight calculated in terms of standard polystyrene as determined by gel permeation chromatography (GPC).

[0027] The peak temperature of tan δ of the thermoplastic elastomer (a) is preferably -60°C or higher, more preferably -50°C or higher, particularly preferably -45°C or higher, and preferably 40°C or lower, more preferably 35°C or lower, particularly preferably 30°C or lower. At temperatures near the peak temperature of tan δ, high vibration-damping properties can be imparted to the vibration-damping laminate. The peak temperature of tan δ can be adjusted to a desired value by adjusting the content of copolymer block (B) in the thermoplastic elastomer (a), or by adjusting the type, bonding form, or glass transition temperature of the monomers constituting the copolymer block (A) or copolymer block (B). The peak temperature of tan δ can be measured by the method described in the Examples below.

[0028] The thermoplastic elastomer (a) can be produced by, for example, the methods described in JP-A-2014-218764 and WO2011 / 040586, but is not limited to these production methods. Some examples of such production methods are described below.

[0029] Thermoplastic elastomer (a) can be produced by, for example, ionic polymerization (e.g., anionic polymerization or cationic polymerization), single-site polymerization, or radical polymerization. When producing a block copolymer comprising at least one copolymer block (A) composed of structural units derived from a conjugated diene compound and at least two copolymer blocks (B) composed of structural units derived from a vinyl aromatic compound by anionic polymerization, for example, an alkyllithium compound or the like is used as a polymerization initiator to sequentially polymerize the vinyl aromatic compound and the conjugated diene compound in an organic solvent inert to the polymerization reaction, such as n-hexane or cyclohexane, followed by the addition of an active hydrogen compound, such as an alcohol, a carboxylic acid, or water, to terminate the polymerization, thereby producing a block copolymer having the desired molecular structure and molecular weight. Polymerization is typically carried out at a temperature of 0 to 80°C for 0.5 to 50 hours.

[0030] When producing a hydrogenated product of a block copolymer, the produced block copolymer is isolated, or preferably, subsequently without isolation, and then subjected to a hydrogenation reaction in an organic solvent inert to the polymerization reaction in the presence of a hydrogenation catalyst, thereby producing the hydrogenated product of the block copolymer.

[0031] When an alkyllithium compound is used as the polymerization initiator, examples of such alkyllithium compounds include alkyllithium compounds in which the alkyl group has 1 to 10 carbon atoms. Among these, methyllithium, ethyllithium, butyllithium, and pentyllithium are preferred. The amount of polymerization initiator such as an alkyllithium compound used is preferably about 0.01 to 0.2 parts by mass per 100 parts by mass of all monomers used in the polymerization.

[0032] In order to achieve the desired content of 3,4-bond units and / or 1,2-bond units derived from isoprene and / or butadiene in the block copolymer serving as the thermoplastic elastomer (a), it is preferable to use a Lewis base as a co-catalyst during polymerization. Examples of Lewis bases include ethers such as dimethyl ether, diethyl ether, tetrahydrofuran (THF), and dioxane; glycol ethers such as ethylene glycol dimethyl ether and diethylene glycol dimethyl ether; amine compounds such as triethylamine, N,N,N',N'-tetramethylethylenediamine (TMEDA), and N-methylmorpholine; nitrogen-containing heterocyclic aromatic compounds such as pyridine; sulfoxides such as dimethyl sulfoxide; and ketones such as acetone and methyl ethyl ketone. These Lewis bases may be used alone or in combination. Among these, ethers and amine compounds are preferred as Lewis bases, with THF and TMEDA being more preferred.

[0033] The amount of the Lewis base used is preferably about 0.1 to 1000 mol, more preferably 0.1 to 100 mol, and even more preferably 1 to 100 mol, relative to 1 mol of lithium atoms in the alkyllithium compound. By appropriately adjusting the amount within this range, the vinyl bond content can be controlled as desired.

[0034] <(b) Hydrocarbon-based softeners> The perforated sheet of the present invention contains a hydrocarbon softener (b) in addition to a thermoplastic elastomer (a). Examples of the hydrocarbon softener (b) include process oils such as paraffinic oil, naphthenic oil, and aromatic oil, and liquid paraffin, with paraffinic oil, naphthenic oil, and other process oils being preferred. These may be used alone or in combination of two or more.

[0035] The production of the hydrocarbon-based softener (b) is not particularly limited, and can be produced by, for example, a conventionally known method. Commercially available products may be used as the hydrocarbon-based softener (b), and typical examples thereof include the Diana Process Oil PW series (paraffinic oil) manufactured by Idemitsu Chemical Co., Ltd., the Diana Process Oil NR series (naphthenic oil) manufactured by Idemitsu Chemical Co., Ltd., and the NOBEL Process Oil AB series (aromatic oil) manufactured by Nikko Oil Products Co., Ltd.

[0036] The content of the hydrocarbon-based softener (b) in the perforated sheet is preferably 10 parts by mass or more, more preferably 12 parts by mass or more, and particularly preferably 15 parts by mass or more, per 100 parts by mass of the thermoplastic elastomer (a), and is preferably 300 parts by mass or less, more preferably 200 parts by mass or less, and particularly preferably 100 parts by mass or less.

[0037] <(c) Polyolefin resin> In one embodiment of the present invention, the perforated sheet of the present invention may contain a polyolefin resin (c) as needed. By using the polyolefin resin (c), the object of the present invention can be achieved to a higher degree. Examples of such polyolefin resins (c) include propylene polymers and ethylene polymers. These may be used alone or in combination of two or more.

[0038] Examples of propylene-based polymers include homopolypropylene and copolymers of other α-olefins with polypropylene, such as random polypropylene and block polypropylene. The stereoregularity is not particularly limited, and may be isotactic polypropylene, syndiotactic polypropylene, atactic polypropylene, etc. Among these, copolymers of other α-olefins with propylene (for example, random copolymers and block copolymers) are preferred. Examples of other α-olefins include ethylene and α-olefins having 4 to 20 carbon atoms, such as ethylene, 1-butene, 1-pentene, 1-hexene, 1-octene, and 4-methyl-1-pentene. One type of other α-olefin may be used alone, or two or more types may be used in combination.

[0039] Examples of ethylene-based polymers include ethylene homopolymers such as low-density polyethylene (LDPE), medium-density polyethylene, and high-density polyethylene (HDPE); and copolymers of other α-olefins with ethylene (e.g., random copolymers and block copolymers). Examples of other α-olefins include α-olefins having 3 to 20 carbon atoms, such as propylene, 1-butene, 1-pentene, 1-hexene, 1-octene, and 4-methyl-1-pentene. These other α-olefins may be used alone or in combination. Specific examples include ethylene-α-olefin copolymers such as ethylene-1-butene copolymer, ethylene-1-hexene copolymer, ethylene-1-heptene copolymer, ethylene-1-octene copolymer, ethylene-4-methyl-1-pentene copolymer, ethylene-1-nonene copolymer, and ethylene-1-decene copolymer.

[0040] The polyolefin resin (c) can be produced by any known method without any particular limitation. Commercially available products may be used as the polyolefin resin (c), and typical examples include the Prime Polypro series, Hi-Zex series, Neo-Zex series, and Ult-Zex series manufactured by Prime Polymer Co., Ltd.

[0041] The content of the polyolefin resin (c) in the perforated sheet is 0 parts by mass or more, preferably 2 parts by mass or more, more preferably 4 parts by mass or more, particularly preferably 5 parts by mass or more, and preferably 50 parts by mass or less, more preferably 20 parts by mass or less, particularly preferably 15 parts by mass or less, per 100 parts by mass of the thermoplastic elastomer (a).

[0042] <(d) Additives> In one embodiment of the present invention, the porous sheet of the present invention may contain an additive (d) as needed. The additive (d) may be used alone or in combination of two or more types. Examples of such additives (d) include flaky inorganic additives such as clay, diatomaceous earth, silica, talc, barium sulfate, calcium carbonate, magnesium carbonate, metal oxides, mica, graphite, and aluminum hydroxide; granular or powdered solid fillers such as various metal powders, wood chips, glass powder, ceramic powder, and granular or powdered polymers; and various other natural or artificial short fibers and long fibers (e.g., straw, wool, glass fiber, metal fiber, and various other polymer fibers). From the viewpoint of reducing the weight of the vibration-damping laminate, hollow fillers such as inorganic hollow fillers such as glass balloons and silica balloons, and organic hollow fillers such as polyvinylidene fluoride and polyvinylidene fluoride copolymers may be blended.

[0043] Furthermore, the perforated sheet may contain various antiblocking agents, heat stabilizers, antioxidants, light stabilizers, ultraviolet absorbers, lubricants, crystal nucleating agents, foaming agents, colorants, flame retardants, etc. depending on the application.

[0044] Examples of antioxidants include phenolic antioxidants such as 2,6-ditert-butyl-p-cresol, 2,6-ditert-butylphenol, 2,4-dimethyl-6-tert-butylphenol, 4,4'-dihydroxydiphenyl, tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane, tetrakis[methylene-3-(3,5-ditert-butyl-4-hydroxyphenyl)propionate]methane, and 3,9-bis{2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy]-1,1-dimethylethyl}-2,4,8,10-tetraoxaspiro-5,5-undecane, phosphite antioxidants, and thioether antioxidants. Among these, phenolic antioxidants and phosphite antioxidants are particularly preferred. The content of the antioxidant is preferably 0.01 to 3 parts by mass, and more preferably 0.05 to 1 part by mass, per 100 parts by mass of the total of the components (a) to (c) contained in the porous sheet of the present invention.

[0045] The flame retardant is not particularly limited, and one or more of various conventionally used flame retardant additives (e.g., organic phosphorus-containing compounds, inorganic phosphorus-containing compounds, organic halogen-containing compounds, inorganic halogen-containing compounds, organic phosphorus-halogen-containing compounds, inorganic phosphorus-halogen-containing compounds, antimony oxide, titanium oxide, metal hydroxides, and hydrous inorganic crystalline compounds) may be used. Among these, halogen-free phosphorus-based flame retardants are preferred, and examples thereof include red phosphorus, organic phosphorus ester compounds, phosphazene compounds, and phosphoramide compounds. Aromatic condensed phosphorus ester compounds are more preferred.

[0046] In the present invention, it is extremely important that the thermoplastic elastomer sheet has multiple through-holes. The inventors have discovered that laminating such a perforated sheet with a fiber-reinforced resin layer results in excellent interlayer adhesion, excellent rigidity, and extremely high vibration-damping properties. Such effects cannot be achieved with fabric products (e.g., woven fabrics, knitted fabrics, and nonwoven fabrics) or synthetic pulp paper (hereinafter, fabric products and synthetic pulp paper may be collectively referred to as "fabric products") made using thermoplastic elastomer fibers without multiple through-holes. The perforated sheet of the present invention is different from such fabric products. The mechanism (reason) by which the presence of multiple through-holes in a thermoplastic elastomer sheet results in excellent interlayer adhesion, excellent rigidity, and extremely high vibration-damping properties in a laminate with a fiber-reinforced resin layer is unclear, but the following is presumed as a non-limiting mechanism. When laminating a thermoplastic elastomer sheet and a prepreg that will form the fiber-reinforced resin layer, the two are usually heated while applying pressure after being stacked. Upon heating, the thermoplastic elastomer contained in the thermoplastic elastomer sheet and the thermosetting resin contained in the prepreg melt and intermix. In the case of perforated sheets, the thermoplastic elastomer and thermosetting resin intermix while maintaining a certain degree of cohesion, and the thermoplastic elastomer remains cohesed to a certain extent even after the thermosetting resin cures. Furthermore, the interface between the thermoplastic elastomer and the thermosetting resin is not strongly bonded (bonded). As a result, the thermoplastic elastomer is easily deformed, and the resulting laminate is presumably exhibiting excellent vibration-damping properties. On the other hand, in the case of fabric products without multiple through holes, the fibers constituting the fabric product are thin, so the thermoplastic elastomer and thermosetting resin intermix more finely and randomly, reducing the degree of freedom of deformation of the thermoplastic elastomer after the thermosetting resin cures. As a result, the resulting laminate is presumably exhibiting poor vibration-damping properties. In both the case of a perforated sheet and a fabric product without multiple through holes, the semi-cured thermosetting resin flows into the through holes in the former case and into the minute gaps in the fabric product in the latter case, and is then hardened by subsequent heat treatment, which is thought to result in excellent interlayer adhesion and rigidity.On the other hand, it was surprising to find that there was a significant difference in vibration damping properties between a perforated sheet and a fabric product that did not have a plurality of through-holes.

[0047] Examples of such sheets having a plurality of through holes include so-called perforated sheets and porous sheets. An example of a perforated sheet is a film (or sheet) in which holes are formed by punching or the like in a film without holes. An example of a porous sheet is a porous membrane with a relatively large pore size. In either case, it is important that there are a plurality of holes penetrating the sheet, and that all or most (preferably more than half, more preferably more than three-quarters) of the width of the thermoplastic elastomer between the plurality of through holes is not as narrow as the diameter of the fibers constituting the fabric product (for example, 100 μm or less). It is also preferable that the size of the holes is uniform. Of these sheets having a plurality of through holes, perforated sheets are more preferred for achieving the objects of the present invention. The thickness of the perforated sheet, particularly the perforated sheet, in the present invention is preferably 100 μm to 3 mm, more preferably 200 μm to 1 mm.

[0048] The aperture ratio of the perforated sheet is preferably 5% or more, more preferably 10% or more, particularly preferably 20% or more, and preferably 80% or less, more preferably 70% or less, particularly preferably 60% or less. The aperture ratio can be determined according to the measurements described in the Examples below. When the aperture ratio is at least the lower limit and at most the upper limit, better interlayer adhesive strength and better vibration damping properties are likely to be obtained.

[0049] The average through-hole diameter of the perforated sheet is preferably 50 μm or more, more preferably 70 μm or more, particularly preferably 80 μm or more, and preferably 6000 μm or less, more preferably 5500 μm or less, particularly preferably 5000 μm or less. The average through-hole diameter refers to the average value of the shortest diameter and the longest diameter of the holes. When the average through-hole diameter is equal to or greater than the lower limit and equal to or less than the upper limit, better interlayer adhesive strength and better vibration damping properties are likely to be obtained. The average through-hole diameter can be determined according to the measurements described in the Examples below.

[0050] The perforated sheet preferably has a perforation density of 1 per cm 2 More than 2 pieces / cm 2 More than 3 / cm is particularly preferable. 2 or more, preferably 80 / cm 2 Less than or equal to 75 particles / cm 2 Less than 70 particles / cm is particularly preferable. 2 When the average through-hole diameter is equal to or greater than the lower limit and equal to or less than the upper limit, it is easy to obtain better interlayer adhesive strength and better vibration damping properties. The through-hole density can be determined according to the measurements described in the Examples below.

[0051] There are no particular limitations on the method for producing the porous sheet. For example, a thermoplastic elastomer resin composition may be prepared, and the porous sheet may be produced from the prepared thermoplastic elastomer resin composition.

[0052] The thermoplastic elastomer resin composition may be prepared by a conventionally known method, for example, using a melt kneader such as a single-screw extruder, a twin-screw extruder, a Banbury mixer, a heating roll, or various kneaders. The set temperature of the melt kneader may be appropriately selected depending on the components contained in the thermoplastic elastomer resin composition. It is usually 150°C to 300°C.

[0053] Examples of producing a perforated sheet from the prepared thermoplastic elastomer resin composition include a method of extruding the thermoplastic elastomer resin composition onto a textured roll, and a method of forming holes in a film obtained by extruding the thermoplastic elastomer resin composition by punching or the like. Alternatively, the desired perforated sheet can be produced by a method for producing a porous separator. Of these methods, a method of forming holes in a film obtained by extruding the thermoplastic elastomer resin composition by punching (hereinafter also referred to as the "punching method") is particularly preferred for achieving the objects of the present invention.

[0054] Examples of methods for obtaining a perforated sheet by punching include a method in which a film is produced from a thermoplastic elastomer resin composition and then a perforated sheet is obtained by various punching methods, and a method in which a cloth product (woven fabric, knitted fabric, or nonwoven fabric) or synthetic pulp paper is produced using a thermoplastic elastomer resin composition and then a perforated sheet is obtained by various punching methods.

[0055] [Fiber reinforced resin layer] The vibration-damping laminate of the present invention comprises a fiber-reinforced resin layer disposed on one or both sides of a perforated sheet. The vibration-damping laminate can be produced, for example, by uniformly impregnating a reinforcing material made of reinforcing fibers with a thermosetting resin composition, and then heating or drying it to a semi-cured state to produce a prepreg, which is then placed on one or both sides of a perforated sheet and heated while applying pressure to cure the thermosetting resin. Pressure can be applied by applying pressure to the stack of prepreg and perforated sheet using a press or the like, or by placing the stack of prepreg and perforated sheet in a pouch or bag or covering it tightly with film or the like and reducing the pressure inside.

[0056] The reinforcing fibers are not particularly limited, and examples thereof include carbon fibers, silica fibers, glass fibers, aramid fibers, boron fibers, alumina fibers, silicon carbide fibers, etc. One of these fibers may be used alone, or two or more may be used in combination. From the viewpoint of easily obtaining a vibration-damping laminate having higher rigidity, the reinforcing fibers are preferably one or more fibers selected from the group consisting of carbon fibers, silica fibers, and glass fibers, and from the viewpoint of lightweight properties, carbon fibers are more preferred.

[0057] Examples of thermosetting resins include epoxy resins, unsaturated polyesters, vinyl ester resins, phenolic resins, cyanate ester resins, polyimides, etc. Among these, epoxy resins are preferred from the viewpoint of adhesiveness.

[0058] The thermosetting resin composition usually contains a curing agent. As such a curing agent, a general curing agent corresponding to the thermosetting resin contained in the thermosetting resin composition may be used. The thermosetting resin composition may also contain any commonly used additives as needed, examples of which include thermoplastic resins such as polyamide, polycarbonate, polyphenylene sulfide, and polyether ether ketone, curing catalysts, and liquid rubber.

[0059] The thermosetting resin composition may be prepared using a melt kneader such as a single-screw extruder, a twin-screw extruder, a Banbury mixer, a heating roll, or various kneaders, or may be prepared using a beaker, a spatula, or the like, as long as uniform kneading is possible.

[0060] Examples of methods for uniformly impregnating a reinforcing material made of reinforcing fibers (e.g., a unidirectional reinforcing fiber sheet, woven fabric, or paper, in which the reinforcing fibers are aligned in one direction) with a thermosetting resin composition include the hot melt method (dry method). The hot melt method involves directly impregnating a reinforcing material with a thermosetting resin composition whose viscosity has been reduced by heating, or by preparing a film coated with the thermosetting resin composition on release paper or the like, and then placing this film on both sides or one side of the reinforcing material, and heating while applying pressure to impregnate the reinforcing material with the resin composition. The conditions for applying pressure and heating may be selected appropriately depending on the components contained in the thermosetting resin composition. A prepreg can be produced by drying or semi-curing after or simultaneously with impregnation.

[0061] The thickness of the prepreg may be selected appropriately depending on the application. The thickness of one prepreg is usually 30 to 300 μm. The prepreg may be used alone or in a stack of multiple sheets depending on the application.

[0062] Commercially available prepregs may be used in the manufacture of the vibration-damping laminate of the present invention, and examples of such commercially available prepregs include Torayca® prepregs.

[0063] [Vibration-damping laminate] A vibration-damping laminate can be produced by placing a prepreg on one or both sides of a perforated sheet and heating it while applying pressure. The conditions for applying pressure and heating can be selected appropriately depending on the type of thermosetting resin contained in the prepreg and the type of thermoplastic elastomer (a) contained in the perforated sheet. Typically, pressure application and heating are carried out at 0.1 to 0.5 MPa and 120 to 220°C for 0.5 to 8 hours.

[0064] The thickness ratio of the perforated sheet to the prepreg in the laminate (perforated sheet thickness / prepreg thickness) can be selected appropriately depending on the application. It is usually 1 / 5 to 1 / 2. When prepregs are present on both sides of the perforated sheet, the above-mentioned prepreg thickness is the total thickness of the prepregs.

[0065] The vibration-damping laminate of the present invention has excellent interlayer adhesion, which can be evaluated by adhesive strength, which can be measured by the method described in the examples below.

[0066] The vibration-damping laminate of the present invention also has excellent rigidity. The rigidity can be evaluated by the flexural modulus, which can be measured by the method described in the Examples below. The flexural modulus is preferably 30 MPa or more, more preferably 40 MPa or more, and even more preferably 50 MPa or more.

[0067] The vibration-damping laminate of the present invention also has extremely excellent vibration-damping properties, and therefore the loss factor η of the vibration-damping laminate at 1000 Hz is 0.016 or more, preferably 0.020 or more, preferably 0.030 or more, more preferably 0.050 or more, and particularly preferably 0.100 or more. The loss factor η can be measured by the method described in the Examples below. There is no particular upper limit to the loss factor η.

[0068] The vibration-damping laminate of the present invention can be used alone or in a combination of two or more layers depending on the application. [Example]

[0069] The present invention will be specifically described below with reference to examples, but the present invention is not limited to these examples. The following examples and comparative examples were evaluated by the methods shown below.

[0070] (1) Glass transition temperature (Tg) The glass transition temperature of the copolymer block contained in the thermoplastic elastomer was measured by taking a portion of the thermoplastic elastomer pellet and using a differential scanning calorimeter (Mettler TA-4000) at a heating rate of 10°C / min.

[0071] (2) Content of 1,2-bonds and 3,4-bonds (vinyl bond content) The thermoplastic elastomer was dissolved in CDCl3, 1 H-NMR measurement was performed (apparatus: JNM-Lambda 500, manufactured by JEOL Ltd., measurement temperature: 50°C). The vinyl bond content (total content of 1,2-bond units and 3,4-bond units) was calculated from the ratio of the total peak area of ​​structural units derived from isoprene, structural units derived from butadiene, or structural units derived from a mixture of isoprene and butadiene to the peak area corresponding to the 1,2-bond units and 3,4-bond units in the structural units of isoprene, the 1,2-bond units and 3,4-bond units in the structural units of butadiene, or, in the case of a mixture of isoprene and butadiene, the peak area corresponding to each of the above bond units.

[0072] (3) Peak temperature of tanδ The loss coefficient (tan δ) of the perforated sheet, woven fabric, nonwoven fabric, or film was determined using a dynamic viscoelasticity measuring device under the following measurement conditions, and the peak temperature of tan δ was read from the resulting graph. Measuring device: Rheogel-E4000 Measurement method: Dynamic viscoelasticity measurement (sine wave) Measurement mode: Temperature dependence Zipper: Pull Frequency: 30Hz Measurement temperature: 23℃ Sample dimensions: width 4.90 mm, thickness 0.3 mm, length 20 mm

[0073] (4) Weight average molecular weight The weight average molecular weight of the thermoplastic elastomer was determined by gel permeation chromatography measurement under the following measurement conditions and conversion into standard polystyrene. GPC:LC Solution (Shimadzu Corporation) Detector: Differential refractometer RID-10A (Shimadzu Corporation) Column: Two TSKgel G4000Hxl columns in series (Tosoh Corporation) Guard column: TSKguardcolumnHxl-L (manufactured by Tosoh Corporation) Solvent: tetrahydrofuran Temperature: 40℃ Flow rate: 1mL / min Concentration: 2mg / mL

[0074] (5)Aperture ratio A 10 cm x 10 cm perforated sheet was copied onto A4-size copy paper at 400% magnification using a copier (Ricoh Co., Ltd., IPSio0 SP6310 RPCS model). Next, the portion of the copy paper other than the copied perforated sheet was cut and removed, and the mass of the copy paper (equivalent to the mass of a thermoplastic elastomer sheet without through holes) (W1 [g]) was measured. Next, the entire portion corresponding to the through holes was cut out from the copy paper for which W1 was measured, and the mass of the cut-out copy paper (equivalent to the mass of thermoplastic elastomer removed by the perforations when through holes are formed in a thermoplastic elastomer sheet without through holes) (W2 [g]) was measured. The opening ratio (%) was calculated according to the following formula: Opening ratio (%)=(W2 / W1)×100

[0075] (6) Average through hole diameter For each through-hole contained in any 1 cm x 1 cm area of ​​the perforated sheet, the shortest diameter and the longest diameter were measured with a vernier caliper, and their average values ​​were calculated. Note that if a portion of a through-hole exists on the periphery of the area, that portion of the through-hole is not included in the through-holes for which the shortest diameter and longest diameter are measured.

[0076] (7) Through-hole density The number of through holes contained in any 1 cm x 1 cm area of ​​the perforated sheet was counted visually. If a portion of the through holes is present on the periphery of the area, the number of through holes is counted according to the area of ​​that portion. For example, if a portion of a circular through hole is present as a semicircle on the periphery of the area, that semicircle portion is counted as half the number of through holes.

[0077] (8) Adhesive strength The fracture surface during the measurement of the flexural modulus was visually observed to confirm whether the fracture was caused by material failure of the thermoplastic elastomer or interlayer delamination between the thermoplastic elastomer sheet and the fiber-reinforced resin layer.

[0078] (9) Flexural modulus Based on JIS K 7074, the flexural modulus was measured using a test piece having a length of 100 mm, a width of 10 mm and a thickness of 1 mm.

[0079] (10) Loss factor η Based on JIS K7391, the loss factor was calculated using the half-width method from the peak of the frequency response function measured using the central excitation method. A system consisting of a Type 3160 oscillator, a Type 2718 amplifier, a Type 4810 exciter, and a Type 8001 acceleration sensor (all manufactured by B&K) was used, along with loss factor measurement software MS18143. The measurement environment was controlled using a thermostatic chamber (PU-3J manufactured by Espec Corporation), and measurements were taken at 23°C. The higher the loss factor, the faster the vibration attenuation and the higher the vibration control performance.

[0080] Preparation of thermoplastic elastomer (a) Thermoplastic elastomers (a-1) to (a-3) were prepared as the thermoplastic elastomer (a) by the following method.

[0081] Thermoplastic elastomer (a-1): Hydrogenated styrene-isoprene-styrene triblock copolymer A nitrogen-purged, dried pressure vessel was charged with 64 L of cyclohexane as a solvent and 0.20 L of sec-butyllithium (10% by mass cyclohexane solution) as a polymerization initiator. 0.3 L of tetrahydrofuran (15 times the stoichiometric ratio of the lithium atoms in the polymerization initiator) was added as an organic Lewis base. After heating to 50°C, 2.3 L of styrene was added and polymerized for 3 hours. 23 L of isoprene was then added and polymerized for 4 hours. 2.3 L of styrene was then added and polymerized for 3 hours. The resulting reaction solution was poured into 80 L of methanol, and the precipitated solid was collected by filtration and dried at 50°C for 20 hours to obtain a triblock copolymer consisting of polystyrene-polyisoprene-polystyrene. 10 kg of the obtained triblock copolymer was dissolved in 200 L of cyclohexane, and palladium carbon (palladium loading: 5% by mass) was added as a hydrogenation catalyst in an amount of 5% by mass relative to the copolymer, and the reaction was carried out for 10 hours under conditions of a hydrogen pressure of 2 MPa and 150° C. After cooling and pressure release, the palladium carbon was removed by filtration, and the filtrate was concentrated and vacuum dried to obtain a hydrogenated product of a triblock copolymer consisting of polystyrene-polyisoprene-polystyrene. The properties of the resulting hydrogenated product were as follows: Weight average molecular weight: 100,000 Content of structural units derived from isoprene: 80% by mass Content of structural units derived from styrene: 20% by mass Content of 3,4-bond units and 1,2-bond units of structural units derived from isoprene: 60 mol%

[0082] Thermoplastic elastomer (a-2): Hydrogenated styrene-isoprene-butadiene-styrene triblock copolymer A hydrogenated styrene-isoprene-butadiene-styrene triblock copolymer was obtained in the same manner as in thermoplastic elastomer (a-1), except that the amount of polymerization initiator sec-butyllithium was changed to 0.18 L and the monomers to be polymerized were 2.2 L of styrene, 6.6 L of isoprene, 7.5 L of 1,3-butadiene, and 2.2 L of styrene. The properties of the resulting hydrogenated product were as follows: Weight average molecular weight: 90,000 Content of structural units derived from isoprene and butadiene: 70% by mass Content of structural units derived from styrene: 30% by mass Content of 3,4-bond units and 1,2-bond units of structural units derived from isoprene and butadiene: 5 mol%

[0083] Thermoplastic elastomer (a-3): Hydrogenated styrene-butadiene-styrene triblock copolymer Into a pressure vessel that had been purged with nitrogen and dried, 55.8 kg of cyclohexane as a solvent and 59 mL of sec-butyllithium (10 mass % cyclohexane solution) as a polymerization initiator were placed, and 99 g of N,N,N',N'-tetramethylethylenediamine as an organic Lewis base was added. Next, a hydrogenated product of a polystyrene-polybutadiene-polystyrene type triblock copolymer was obtained in the same manner as in the thermoplastic elastomer (a-1), except that 1.84 kg of styrene, 8.57 kg of butadiene, and 1.84 kg of styrene were used as the monomers to be polymerized and the hydrogenation reaction time was changed to 5 hours. The properties of the resulting hydrogenated product were as follows: Weight average molecular weight: 280,000 Content of structural units derived from butadiene: 66% by mass Content of structural units derived from styrene: 34% by mass Content of 3,4-bond units and 1,2-bond units of structural units derived from butadiene: 33 mol%

[0084] Hydrocarbon-based softener (b) Hydrocarbon-based softener (b-1) Diana Process Oil PW-380 (product name), manufactured by Idemitsu Petrochemical Co., Ltd., paraffinic oil, kinematic viscosity (40°C): 381.6 mm 2 / s, ring analysis paraffin: 73%, ring analysis naphthene: 27%, weight average molecular weight: 1304 Hydrocarbon-based softener (b-2) Diana Process Oil PW-90 (product name), manufactured by Idemitsu Petrochemical Co., Ltd., paraffinic oil, kinematic viscosity (40°C): 95.5 mm 2 / s, ring analysis paraffin: 71%, ring analysis naphthene: 29%, weight average molecular weight: 790

[0085] Polyolefin polymer (c) Polyolefin polymer (c-1) Polypropylene: Prime Polypro F219DA (trade name), manufactured by Prime Polymer Co., Ltd., MFR (230°C): 8.0 g / 10 min Polyolefin polymer (c-2) Polypropylene: Prime Polypro J108M (product name), manufactured by Prime Polymer Co., Ltd., MFR (230°C): 45 g / 10 min

[0086] Prepreg fabrication The epoxy resin composition was applied to release paper using a reverse roll coater to prepare a resin film. Next, a sheet of unidirectionally aligned carbon fiber "TORAYCA (registered trademark)" T800SC-24K (manufactured by Toray Industries, Inc., tensile modulus: 294 GPa, tensile strength: 5880 MPa) was placed on top of the prepared resin film, and another prepared resin film was then placed on top of that. The carbon fiber was impregnated with the epoxy resin composition by heating while applying pressure using a press, to prepare a unidirectional prepreg. The carbon fiber mass per unit area of ​​the unidirectional prepreg was 125 g / m 2 The fiber mass content was 75 mass %, and the thickness was 100 μm.

[0087] Fabrication of laminated prepreg Five of the unidirectional prepregs were stacked so that the fiber directions were alternately perpendicular to each other, and heated at 200°C and 0.5 MPa for 3 minutes while applying pressure using a press to produce a 5-ply laminated prepreg.

[0088] Examples 1 to 4 After mixing the components according to the formulation listed in Table 1 below, the mixture was melt-kneaded at 190°C using a twin-screw extruder (diameter 46 mm, L / D = 46) to obtain a pellet-shaped thermoplastic elastomer resin composition. The resulting thermoplastic elastomer resin composition was extruded at a nozzle temperature of 200°C to obtain a 300 μm-thick film. The resulting film was punched to obtain a thermoplastic elastomer sheet with multiple through-holes. The resulting perforated sheet was placed between two 5-ply laminated prepregs, and the stack was then tightly covered with a nylon film. This was heated in an autoclave at 135°C and an internal pressure of 588 kPa for 2 hours to cure the epoxy resin and produce a vibration-damping laminate.

[0089] Example 5 A vibration-damping laminate was produced in the same manner as in Example 2, except that the carbon fiber in the prepreg was changed to glass fiber ("RS110QL-520" (trade name) manufactured by Nitto Boseki Co., Ltd.).

[0090] Comparative Example 1 Instead of the perforated sheet, a woven fabric (basis weight: 52 g / m) was obtained by weaving fibers made of a thermoplastic elastomer prepared according to the formulation shown in Table 1. 2 A vibration-damping laminate was obtained in the same manner as in Example 1 except that the same weight per unit area and thickness as in Example 1 of JP-A 2015-193751 (300 μm) was used.

[0091] Comparative Example 2 Instead of the perforated sheet, a nonwoven fabric (basis weight: 80 g / m) was produced using fibers made of a thermoplastic elastomer prepared according to the formulation shown in Table 1. 2 A vibration-damping laminate was obtained in the same manner as in Example 1, except that a laminate of 1000 kJ / cm² (thickness: 400 μm) was used.

[0092] Comparative Example 3 A vibration-damping laminate was obtained in the same manner as in Example 1, except that a 0.2 mm thick film made of a thermoplastic elastomer prepared according to the formulation shown in Table 1 was used instead of the perforated sheet.

[0093] Comparative Example 4 Adhesive tape (acrylic adhesive tape with a thickness of 0.1 mm) was attached to both sides of the perforated sheet produced in Example 2, and urethane synthetic leather (thickness of 0.7 mm) was attached to one side of the tape to obtain a laminate.

[0094] The evaluation results of Examples 1 to 5 and Comparative Examples 1 to 4 are shown in Table 1. [Table 1]

[0095] Table 1 shows that the vibration-damping laminate of the present invention has high adhesive strength, a high flexural modulus, and an extremely high loss factor. This indicates that the vibration-damping laminate of the present invention has excellent interlayer adhesion, excellent rigidity, and extremely excellent vibration-damping properties. In the vibration-damping laminate of the present invention, the semi-cured thermosetting resin flows into the through-holes and is cured by heat treatment, resulting in excellent interlayer adhesion and rigidity. However, the use of a specific thermoplastic elastomer sheet allows the thermoplastic elastomer to exist in a state that is easily deformed in the laminate, which is thought to ensure extremely excellent vibration-damping properties. On the other hand, the comparative examples using woven fabric and nonwoven fabric have low loss factors and poor vibration damping. The comparative examples using film also have low adhesive strength and modulus, which is thought to be due to poor interfacial adhesion between the film and the epoxy resin. The comparative example using polyurethane synthetic leather instead of a fiber-reinforced resin layer has good adhesion between the polyurethane synthetic leather and the perforated sheet, but does not achieve the desired rigidity and vibration damping. [Industrial Applicability]

[0096] The vibration-damping laminate of the present invention has excellent interlayer adhesion and excellent rigidity, while also having extremely excellent vibration-damping properties, and therefore can be suitably used in applications requiring high strength, high dimensional accuracy, and high vibration-damping properties, such as sporting goods such as rackets (e.g., tennis rackets and badminton rackets), skis, and snowboards, and parts or structural materials that constitute moving bodies such as automobiles, aircraft, railway vehicles, and ships.

Claims

1. A thermoplastic elastomer sheet comprising a thermoplastic elastomer (a) containing at least one copolymer block (A) having a glass transition temperature of 30°C or lower and having a plurality of through holes; and a fiber-reinforced resin layer disposed on one or both sides of the thermoplastic elastomer sheet; A vibration-damping laminate comprising: the thermoplastic elastomer (a) is a block copolymer comprising at least one copolymer block (A) comprising structural units derived from a conjugated diene compound and at least two copolymer blocks (B) comprising structural units derived from a vinyl aromatic compound, and / or a hydrogenated product of the block copolymer; The weight average molecular weight of the thermoplastic elastomer (a) is 40,000 or more and 500,000 or less, the thermoplastic elastomer sheet has an opening ratio of 5% or more and 80% or less, A vibration-damping laminate having a loss factor η of 0.016 or more at 1000 Hz.

2. 2. The vibration-damping laminate according to claim 1, wherein the thermoplastic elastomer (a) has a weight-average molecular weight of 70,000 or more and 350,000 or less.

3. In the thermoplastic elastomer sheet, for 100 parts by mass of the thermoplastic elastomer (a), the content of the hydrocarbon-based softener (b) is 10 parts by mass or more and 300 parts by mass or less, The content of the polyolefin resin (c) is 50 parts by mass or less. The vibration-damping laminate according to claim 1 or 2.

4. In the thermoplastic elastomer sheet, for 100 parts by mass of the thermoplastic elastomer (a), the content of the hydrocarbon-based softener (b) is 10 parts by mass or more and 300 parts by mass or less, The content of the polyolefin resin (c) is 2 parts by mass or more and 50 parts by mass or less. The vibration-damping laminate according to any one of claims 1 to 3.

5. 5. The vibration-damping laminate according to claim 1, wherein the thermoplastic elastomer sheet has an opening ratio of 20% or more and 60% or less.

6. 6. The vibration-damping laminate according to claim 1, wherein the thermoplastic elastomer sheet has an average through-hole diameter of 50 μm or more and 6000 μm or less.

7. The thermoplastic elastomer sheet is 1 piece / cm ２ Above, 80 pieces / cm ２ 7. The vibration-damping laminate according to claim 1, having the following through-hole density:

8. The vibration-damping laminate according to any one of claims 1 to 7, wherein the fiber-reinforced resin layer comprises one or more fibers selected from the group consisting of carbon fibers, silica fibers, glass fibers, aramid fibers, boron fibers, alumina fibers, and silicon carbide fibers.

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