WO2021106848A1

WO2021106848A1 - Adhesive composition, adhesive sheet, laminate, and printed wiring board

Info

Publication number: WO2021106848A1
Application number: PCT/JP2020/043610
Authority: WO
Inventors: 遼薗田; 哲生川楠
Original assignee: 東洋紡株式会社
Priority date: 2019-11-29
Filing date: 2020-11-24
Publication date: 2021-06-03
Also published as: CN114514300B; CN114514300A; JPWO2021106848A1; TW202130770A; KR20220107147A; JP6919777B1

Abstract

[Problem] To provide an adhesive composition which has a high adhesion to a metal substrate and a resin substrate such as a liquid crystal polymer or syndiotactic polystyrene as well as to a conventional polyimide or polyester film, and also has excellent low dielectric characteristics and pot life, and from which high solder heat resistance can be achieved. [Solution] This adhesive composition contains (a) an acid-modified polyolefin, (b) a phenol resin having a polycyclic structure, and (c) an epoxy resin.

Description

Adhesive compositions, adhesive sheets, laminates and printed wiring boards

The present invention relates to an adhesive composition. More specifically, the present invention relates to an adhesive composition used for adhering a resin base material to a resin base material or a metal base material. In particular, the present invention relates to an adhesive composition for a flexible printed wiring board (hereinafter abbreviated as FPC), and an adhesive sheet, a laminate and a printed wiring board containing the same.

Since the flexible printed wiring board (FPC) has excellent flexibility, it can be used for multi-functionality and miniaturization of personal computers (PCs) and smartphones, and therefore, an electronic circuit board is incorporated in a narrow and complicated interior. It is often used for. In recent years, electronic devices have become smaller, lighter, higher in density, and have higher output, and due to these trends, the demand for the performance of wiring boards (electronic circuit boards) has become more and more sophisticated. In particular, as the speed of transmission signals in FPCs increases, the frequency of signals is increasing. Along with this, there is an increasing demand for FPCs having low dielectric properties (low dielectric constant, low dielectric loss tangent) in the high frequency region. As for the base material used for FPC, not only the conventional polyimide (PI) and polyethylene terephthalate (PET), but also the base film such as liquid crystal polymer (LCP) and syndiotactic polystyrene (SPS) having low dielectric properties. Has been proposed. In order to achieve such low dielectric properties, measures have been taken to reduce the dielectric loss of the FPC base material and the adhesive. As an adhesive, development is underway with a combination of polyolefin and epoxy (Patent Document 1) and a combination of elastomer and epoxy (Patent Document 2).

WO2016 / 047289 WO2014 / 147903

However, in Patent Document 1, it cannot be said that the heat resistance of the reinforcing plate and the adhesive used between the layers is excellent. Further, in Patent Document 2, the storage stability after compounding, which is important at the time of use, was not sufficient.

As a result of diligent studies to solve the above problems, the present invention contains not only a conventional polyimide film but also a resin base material such as a liquid crystal polymer or syndiotactic polystyrene and copper as an adhesive composition having a specific composition. We have found that it has high adhesiveness to a metal base material such as foil, and also has excellent low dielectric properties (electrical properties), solder heat resistance, and pot life after compounding, and has completed the present invention. It is a thing.

That is, the present invention has good adhesiveness not only to polyimide but also to various resin substrates such as liquid crystal polymers and syndiotactic polystyrene and metal substrates, and has low dielectric properties (electrical properties) and solder. An object of the present invention is to provide an adhesive composition having excellent heat resistance and pot life.

An adhesive composition containing an acid-modified polyolefin (a), a phenol resin (b) having a polycyclic structure, and an epoxy resin (c).

The phenol resin (b) having a polycyclic structure is preferably a phenol resin having a tricyclodecane skeleton, and more preferably has a carbonate skeleton. The acid value of the acid-modified polyolefin (a) is preferably 5 to 40 mgKOH / g.

It is preferable to further contain polycarbodiimide (d). Further, with respect to 100 parts by mass of the acid-modified polyolefin (a), 0.05 to 120 parts by mass of the phenol resin (b) having a polycyclic structure, 0.1 to 60 parts by mass of the epoxy resin (c), and It is preferable to contain 0.1 to 30 parts by mass of polycarbodiimide (d).

The adhesive composition preferably has a relative permittivity (ε _c ) of 3.0 or less and a dielectric loss tangent (tan δ) of 0.02 or less at 1 GHz.

An adhesive sheet or laminate containing the adhesive composition. A printed wiring board containing the laminate as a component.

The adhesive composition according to the present invention has good adhesiveness not only to polyimide but also to various resin substrates such as liquid crystal polymers and syndiotactic polystyrene and metal substrates, and has low dielectric properties (electricity). (Characteristics), excellent in solder heat resistance and pot life.

<Acid-modified polyolefin (a)>
The acid-modified polyolefin (a) used in the present invention (hereinafter, also simply referred to as the component (a)) is not limited, but at least one of α, β-unsaturated carboxylic acid and its acid anhydride is added to the polyolefin resin. It is preferably obtained by grafting. The polyolefin resin is a hydrocarbon such as homopolymerization of an olefin monomer exemplified by ethylene, propylene, butene, butadiene, isoprene, or copolymerization with other monomers, and hydrides and halides of the obtained polymer. Refers to a polymer whose main component is the skeleton. That is, the acid-modified polyolefin is obtained by grafting at least one of α, β-unsaturated carboxylic acid and its acid anhydride to at least one of polyethylene, polypropylene and a propylene-α-olefin copolymer. Is preferred.

The propylene-α-olefin copolymer is a copolymer of propylene as a main component and α-olefin. As the α-olefin, for example, one or several kinds of ethylene, 1-butene, 1-heptene, 1-octene, 4-methyl-1-pentene, vinyl acetate and the like can be used. Among these α-olefins, ethylene and 1-butene are preferable. The ratio of the propylene component to the α-olefin component of the propylene-α-olefin copolymer is not limited, but the propylene component is preferably 50 mol% or more, and more preferably 70 mol% or more.

Examples of at least one of α, β-unsaturated carboxylic acid and its acid anhydride include maleic acid, itaconic acid, citraconic acid and their acid anhydrides. Among these, acid anhydride is preferable, and maleic anhydride is more preferable. Specific examples thereof include maleic anhydride-modified polypropylene, maleic anhydride-modified propylene-ethylene copolymer, maleic anhydride-modified propylene-butene copolymer, maleic anhydride-modified propylene-ethylene-butene copolymer and the like. These acid-modified polyolefins can be used alone or in combination of two or more.

The lower limit of the acid value of the acid-modified polyolefin (a) is preferably 5 mgKOH / g or more, more preferably 6 mgKOH / g or more, from the viewpoint of heat resistance and adhesion to a resin base material or a metal base material. , More preferably 7 mgKOH / g or more. By setting the value to the lower limit or more, the compatibility with the epoxy resin (c) becomes good, and excellent adhesive strength can be exhibited. In addition, the crosslink density is high and the solder heat resistance is good. The upper limit is preferably 40 mgKOH / g or less, more preferably 30 mgKOH / g or less, and further preferably 20 mgKOH / g or less. When the value is not more than the upper limit value, the adhesiveness is improved. In addition, the viscosity and stability of the solution are improved, and excellent pot life can be exhibited. Furthermore, the manufacturing efficiency is improved.

The number average molecular weight (Mn) of the acid-modified polyolefin (a) is preferably in the range of 10,000 to 50,000. It is more preferably in the range of 15,000 to 45,000, further preferably in the range of 20,000 to 40,000, and particularly preferably in the range of 22,000 to 38,000. By setting the value to the lower limit or more, the cohesive force becomes good and excellent adhesiveness can be exhibited. Further, when the value is not more than the upper limit value, the fluidity is excellent and the operability is good.

The acid-modified polyolefin (a) is preferably a crystalline acid-modified polyolefin. Crystallinity as used in the present invention means that the temperature is raised from −100 ° C. to 250 ° C. at 20 ° C./min using a differential scanning calorimeter (DSC) and a clear melting peak is shown in the heating process. Point to.

The melting point (Tm) of the acid-modified polyolefin (a) is preferably in the range of 50 ° C. to 120 ° C. It is more preferably in the range of 60 ° C to 100 ° C, and most preferably in the range of 70 ° C to 90 ° C. When it is set to the above lower limit value or more, the cohesive force derived from the crystal becomes good, and excellent adhesiveness and solder heat resistance can be exhibited. Further, when the value is not more than the upper limit, the solution stability and fluidity are excellent, and the operability at the time of adhesion is improved.

The heat of fusion (ΔH) of the acid-modified polyolefin (a) is preferably in the range of 5 J / g to 60 J / g. It is more preferably in the range of 10 J / g to 50 J / g, and most preferably in the range of 20 J / g to 40 J / g. When it is set to the above lower limit value or more, the cohesive force derived from the crystal becomes good, and excellent adhesiveness and solder heat resistance can be exhibited. Further, when the value is not more than the upper limit, the solution stability and fluidity are excellent, and the operability at the time of adhesion is improved.

The method for producing the acid-modified polyolefin (a) is not particularly limited, and for example, a radical graft reaction (that is, a radical species is generated for a polymer serving as a main chain, and the radical species is used as a polymerization initiation point to form an unsaturated carboxylic acid (Reaction of graft polymerization of acid anhydride), and the like.

The radical generator is not particularly limited, but it is preferable to use an organic peroxide. The organic peroxide is not particularly limited, but is di-tert-butylperoxyphthalate, tert-butylhydroperoxide, dicumyl peroxide, benzoyl peroxide, tert-butylperoxybenzoate, tert-butylperoxy-. Peroxides such as 2-ethylhexanoate, tert-butylperoxypivalate, methylethylketone peroxide, di-tert-butyl peroxide, lauroyl peroxide; azobisisobutyronitrile, azobisisopropionitrile, etc. Examples include azonitriles.

<Phenol resin (b) having a polycyclic structure>
The phenol resin (b) having a polycyclic structure used in the present invention (hereinafter, also simply referred to as the component (b)) is not limited as long as it is a phenol resin having one or more polycyclic structures in one molecule. The polycyclic structure refers to a structure in which a plurality of ring structures mainly composed of carbon are bonded, for example, an aromatic skeleton such as naphthalene, anthracene, indane, and tetralin, and an alicyclic structure such as decalin, norbornane, and tricyclodecane. Examples include structures having a skeleton. By having a polycyclic structure, the free volume of the resin is increased and low dielectric properties are exhibited. It also exhibits heat resistance. The number of polycyclic structures contained in one molecule is preferably 2 or more, and more preferably 3 or more. Further, it is preferably 10 or less, more preferably 8 or less, and further preferably 5 or less. Within the above range, excellent dielectric properties can be exhibited. The polycyclic structure is not particularly limited, but is preferably an alicyclic skeleton having 4 to 30 carbon atoms, more preferably an alicyclic skeleton having 5 to 25 carbon atoms, and further preferably 8 to 20 carbon atoms. The alicyclic skeleton of the above, particularly preferably an alicyclic skeleton having 10 to 15 carbon atoms. Specific examples of the polycyclic structure include bicyclic alicyclic compounds such as bicyclobutane, bicyclopentane, bicyclohexane, bicycloheptan (norbornan), bicyclooctane, bicyclononane, and bicyclodecane, which may have optionally substituents. Ring structure; tricyclic alicyclic structure such as tricyclooctane, tricyclononane, tricyclodecane, tricycloundecane, tricyclododecane, etc., which may have a substituent arbitrarily; Good alicyclic structures of tetracyclic or higher such as tetracyclodecane, tetracycloundecane, tetracyclododecane; aromatic structures such as naphthalene, anthracene, indane, tetralin which may optionally have substituents can be mentioned. Further, the alicyclic structure may have an unsaturated bond, and examples thereof include bicyclohexene, bicyclohexene, bicyclohexene, bicyclooctene, bicyclononene, and bicyclodecene, which may have an optionally substituent. These polycyclic structures may have one type or two or more types in one molecule of the phenol resin. The substituent is not particularly limited, but is an alkyl group such as a methyl group, an ethyl group or a propyl group; an alkoxy group such as a methoxy group or an ethoxy group; a thioalkoxy group such as a thiomethoxy group or a thioethoxy group; a hydroxyl group, an amino group or the like. Can be mentioned.

Among the polycyclic structures, a tricyclic alicyclic structure such as tricyclooctane, tricyclononane, tricyclodecane, tricycloundecane, and tricyclododecane, which may have a substituent, is preferable. It is preferably a tricyclodecane which may have a substituent. ^{Among them, tricyclo [5.2.1.0 2,6} ] decane, tricyclo [6.1.1.0 ^2,6 ] decane, tricyclo [6.1.1.0 ^2, ] which may have a substituent may be present. ⁷ ] Decane, tricyclo [3.3.1.1 ^3,7 ] decane (adamantane) is preferable, and tricyclo [5.2.1.0 ^2,6 ] decane which may have a substituent is particularly preferable. is there. Specifically, 3,4-dimethylene-tricyclo [5.2.1.0 ^2,6 ] decane, 3,5-dimethylene-tricyclo [5.2.1.0 ^2,6 ] decane, 3,8 -Dimethylene-tricyclo [5.2.1.0 ^2,6 ] decane, 3,9-dimethylene-tricyclo [5.2.1.0 ^2,6 ] decane, 8,9-dimethylene-tricyclo [5.2] .1.0 ^2,6 ] decane is mentioned, and among them, 3,5-dimethylene-tricyclo [5.2.1.0 ^2,6 ] decane is preferable.

The phenol resin (b) having a polycyclic structure preferably further has a carbonate skeleton. By having the carbonate skeleton, it is possible to further impart flexibility to the adhesive composition while maintaining adhesiveness and electrical properties. The amount of the carbonate skeleton contained in the phenol resin (b) having a polycyclic structure is preferably 2 or more, more preferably 3 or more, and further preferably 4 or more in one molecule. Further, it is preferably 10 or less, more preferably 8 or less, and further preferably 6 or less.

The phenol resin (b) having a polycyclic structure preferably has a structure represented by the general formula (1).

In the general formula (1), m and n are each independently preferably an integer of 1 or more and 10 or less, more preferably 8 or less, further preferably 5 or less, and particularly preferably 2 or less. ..

Further, the phenol resin (b) having a polycyclic structure is more preferably the general formula (2).

In the general formula (2), m and n have the same meanings as described above. p is preferably an integer of 1 or more and 10 or less, more preferably 2 or more, still more preferably 3 or more, and particularly preferably 4 or more. Further, it is preferably 8 or less, and more preferably 5 or less. R ₁ and R ₂ are aromatic hydrocarbons that may independently have a substituent, and as the substituent, an aliphatic hydrocarbon that may further have a substituent and further having a substituent. It is preferably an alicyclic hydrocarbon which may have a substituent, or an aromatic hydrocarbon which may further have a substituent.

It is preferable that R ₁ and R ₂ independently have the structure of the formula (11) or the formula (12), respectively.

In formulas (11) and (12), R ₃ and R ₄ are independently alkyl groups having 1 to 10 carbon atoms, alkoxy groups having 1 to 10 carbon atoms, alkenyl groups having 2 to 10 carbon atoms, or substitutions. It is preferably a phenyl group which may have a group. It is more preferably an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 1 to 5 carbon atoms, and further preferably an alkyl group having 1 to 3 carbon atoms or an alkenyl group having 2 to 3 carbon atoms. Specifically, it is preferably a methyl group, an ethyl group, an n-propyl group, an isopropyl group, or a propenyl group. x and y are independently integers of 0 to 4, preferably integers of 0 to 3, more preferably 0 or 1, and particularly preferably 1. Z ₁ is preferably an integer of 0 to 5, more preferably an integer of 1 to 3, still more preferably 1 or 2, and particularly preferably 1. Z ₂ is preferably an integer of 0 to 5, more preferably an integer of 1 to 3, still more preferably 1 or 2, and particularly preferably 1. The hydroxyl group or ether group may be in the ortho-position, meta-position or para-position with respect to the benzyl group, but is preferably in the para-position. * Indicates a bond with the oxygen atom of the general formula (2).

The number average molecular weight of the component (b) is preferably 5000 or less, more preferably 4000 or less, and even more preferably 3500 or less. The number average molecular weight of the component (b) is preferably 500 or more, and more preferably 700 or more. By setting the number average molecular weight of the component (b) to the lower limit value or more, the flexibility of the obtained adhesive layer can be improved. On the other hand, by setting the number average molecular weight of the component (b) to the upper limit or less, the solubility in an organic solvent can be improved.

The content of the component (b) is preferably 0.05 parts by mass or more, more preferably 1 part by mass or more, and further preferably 5 parts by mass or more with respect to 100 parts by mass of the component (a). is there. By setting the value to the lower limit or more, excellent solder heat resistance can be exhibited. Further, it is preferably 120 parts by mass or less, more preferably 100 parts by mass or less, further preferably 90 parts by mass or less, and particularly preferably 80 parts by mass or less. By setting the value to the upper limit or less, excellent adhesiveness and solder heat resistance can be exhibited.

<Epoxy resin (c)>
The epoxy resin (c) used in the present invention (hereinafter, also simply referred to as the component (c)) is not particularly limited as long as it has an epoxy group in the molecule, but preferably two or more in the molecule. It has an epoxy group. Specifically, although not particularly limited, biphenyl type epoxy resin, naphthalene type epoxy resin, bisphenol A type epoxy resin, bisphenol F type epoxy resin, novolak type epoxy resin, alicyclic epoxy resin, dicyclopentadiene type epoxy resin, At least one selected from the group consisting of tetraglycidyl diaminodiphenylmethane, triglycidyl paraaminophenol, tetraglycidyl bisaminomethylcyclohexanone, N, N, N', N'-tetraglycidyl-m-xylene diamine, and epoxy-modified polybutadiene. Can be used. Preferably, it is a biphenyl type epoxy resin, a novolak type epoxy resin, a dicyclopentadiene type epoxy resin, triglycidyl paraaminophenol or an epoxy-modified polybutadiene. More preferably, it is a dicyclopentadiene type epoxy resin, a novolac type epoxy resin or triglycidyl paraaminophenol.

In the adhesive composition of the present invention, the content of the epoxy resin (c) is preferably 0.1 part by mass or more, more preferably 0.5 parts by mass, based on 100 parts by mass of the acid-modified polyolefin (a). It is by mass or more, more preferably 1 part by mass or more, and particularly preferably 2 parts by mass or more. By setting the value to the lower limit or more, a sufficient curing effect can be obtained, and excellent adhesiveness and solder heat resistance can be exhibited. Further, it is preferably 60 parts by mass or less, more preferably 50 parts by mass or less, further preferably 40 parts by mass or less, and particularly preferably 35 parts by mass or less. By setting the value to the upper limit or less, the pot life property and the low dielectric property are improved. That is, within the above range, an adhesive composition having excellent low dielectric properties in addition to adhesiveness, solder heat resistance and pot life property can be obtained.

<Polycarbodiimide (d)>
The polycarbodiimide (d) used in the present invention (hereinafter, also simply referred to as the component (d)) is not particularly limited as long as it has a carbodiimide group in the molecule. It is preferably a polycarbodiimide having two or more carbodiimide groups in the molecule. By using polycarbodiimide, the carboxyl group of the acid-modified polyolefin (a) reacts with the carbodiimide group, the interaction between the adhesive composition and the substrate can be enhanced, and the adhesiveness can be improved.

In the adhesive composition of the present invention, the content of the polycarbodiimide (d) is preferably 0.1 part by mass or more, more preferably 0.5 parts by mass, based on 100 parts by mass of the acid-modified polyolefin (a). It is by mass or more, more preferably 1 part by mass or more, and particularly preferably 2 parts by mass or more. When it is set to the above lower limit value or more, the interaction with the base material is exhibited and the adhesiveness is improved. Further, it is preferably 30 parts by mass or less, more preferably 25 parts by mass or less, further preferably 20 parts by mass or less, still more preferably 15 parts by mass or less, and particularly preferably 10 parts by mass or less. Is. By setting the value to the upper limit or less, excellent pot life and low dielectric properties can be exhibited. That is, within the above range, an adhesive composition having excellent low dielectric properties in addition to adhesiveness, solder heat resistance and pot life property can be obtained. The content of polycarbodiimide (d) with respect to the epoxy resin (c) is preferably 5 parts by mass or more, more preferably 10 parts by mass or more, and further preferably 15 parts by mass or more with respect to 100 parts by mass of the epoxy resin (c). Is. Further, it is preferably 100 parts by mass or less, more preferably 80 parts by mass or less, and further preferably 60 parts by mass or less. Within the above range, an adhesive composition having a good balance of solder heat resistance and low dielectric properties can be obtained.

<Adhesive composition>
The adhesive composition of the present invention contains the three types of resins (a) to (c), and thus contains a low-polarity resin base material such as a liquid crystal polymer (LCP) or syndiotactic polystyrene (SPS). It can exhibit excellent adhesiveness to a metal substrate, pot life, electrical properties (low dielectric properties), and heat resistance. That is, the adhesive coating film (adhesive layer) after the adhesive composition is applied to the base material and cured can exhibit excellent low dielectric constant characteristics.

The adhesive composition of the present invention can further contain an organic solvent. The organic solvent used in the present invention is not particularly limited as long as it dissolves the acid-modified polyolefin (a), the phenol resin (b) having a polycyclic structure, the epoxy resin (c), and the polycarbodiimide (d). .. Specifically, for example, aromatic hydrocarbons such as benzene, toluene and xylene, aliphatic hydrocarbons such as hexane, heptane, octane and decane, and alicyclic hydrocarbons such as cyclohexane, cyclohexene, methylcyclohexane and ethylcyclohexane. Halogenized hydrocarbons such as hydrogen, trichloroethylene, dichloroethylene, chlorobenzene and chloroform, alcohol solvents such as methanol, ethanol, isopropyl alcohol, butanol, pentanol, hexanol, propanediol and phenol, acetone, methylisobutylketone, Ketone solvents such as methyl ethyl ketone, pentanone, hexanone, cyclohexanone, isophorone, acetophenone, cell solves such as methyl cellsolve and ethyl cell solve, ester solvents such as methyl acetate, ethyl acetate, butyl acetate, methyl propionate, butyl formate, Ethylene glycol mono n-butyl ether, ethylene glycol mono iso-butyl ether, ethylene glycol mono t e r t-butyl ether, diethylene glycol mono n-butyl ether, diethylene glycol mono iso-butyl ether, triethylene glycol mono n-butyl ether, tetraethylene glycol mono n- A glycol ether solvent such as butyl ether can be used, and one or more of these can be used in combination. Methylcyclohexane and toluene are particularly preferable because of their work environment and dryness.

The organic solvent is preferably in the range of 100 to 1000 parts by mass, more preferably in the range of 200 to 900 parts by mass, and 300 to 800 parts by mass with respect to 100 parts by mass of the acid-modified polyolefin (a). Most preferably it is in the range. When it is at least the above lower limit value, the liquid and pot life properties are improved. Further, setting the value to the upper limit or less is advantageous in terms of manufacturing cost and transportation cost.

The adhesive composition according to the present invention preferably has a relative permittivity (ε _c ) of 3.0 or less at a frequency of 1 GHz. It is more preferably 2.6 or less, and even more preferably 2.3 or less. The lower limit is not particularly limited, but is 2.0 in practice. Further, the relative permittivity (ε) in the entire region of the frequency 1 GHz to 60 GHz is preferably 3.0 or less, more preferably 2.6 or less, and further preferably 2.3 or less.

The adhesive composition according to the present invention preferably has a dielectric loss tangent (tan δ) at a frequency of 1 GHz or less. It is more preferably 0.01 or less, and even more preferably 0.008 or less. The lower limit is not particularly limited, but is 0.0001 in practice. Further, the dielectric loss tangent (tanδ) in the entire region of the frequency 1 GHz to 60 GHz is preferably 0.02 or less, more preferably 0.01 or less, and further preferably 0.005 or less.

In the present invention, the relative permittivity (ε _c ) and the dielectric loss tangent (tan δ) can be measured as follows. That is, the adhesive composition is applied to the release base material so that the thickness after drying is 25 μm, and dried at about 130 ° C. for about 3 minutes. Then, it is heat-treated at about 140 ° C. for about 4 hours to be cured, and the cured adhesive composition layer (adhesive layer) is peeled off from the release film. _{The relative permittivity (ε c} ) and the dielectric loss tangent (tan δ) of the adhesive composition layer after peeling at a frequency of 1 GHz are measured. _{Specifically, the relative permittivity (ε c} ) and the dielectric loss tangent (tan δ) can be calculated from the measurement by the cavity resonator perturbation method.

Further, the adhesive composition of the present invention may further contain other components as required. Specific examples of such components include flame retardants, tackifiers, fillers, and silane coupling agents.

<Flame retardant>
A flame retardant may be added to the adhesive composition of the present invention, if necessary. Examples of the flame retardant include bromine-based, phosphorus-based, nitrogen-based, and metal hydroxide compounds. Among them, a phosphorus-based flame retardant is preferable, and a known phosphorus-based flame retardant such as a phosphate ester such as trimethyl phosphate, triphenyl phosphate, tricresyl phosphate or the like, a phosphate such as aluminum phosphite, or phosphazene can be used. .. These may be used alone or in any combination of two or more. When the flame retardant is contained, the flame retardant is preferably contained in the range of 1 to 200 parts by mass, more preferably in the range of 5 to 150 parts by mass, based on 100 parts by mass of the total of the components (a) to (d). The range of 10 to 100 parts by mass is most preferable. Within the above range, flame retardancy can be exhibited while maintaining adhesiveness, solder heat resistance and electrical characteristics.

<Adhesive imparting agent>
A tackifier may be added to the adhesive composition of the present invention, if necessary. Examples of the tackifier include polyterpene resin, rosin resin, aliphatic petroleum resin, alicyclic petroleum resin, copolymer petroleum resin, styrene resin, hydrogenated petroleum resin, and the like for the purpose of improving adhesive strength. Used in. These may be used alone or in any combination of two or more. When the tackifier is contained, it is preferably contained in the range of 1 to 200 parts by mass, more preferably in the range of 5 to 150 parts by mass, based on 100 parts by mass of the total of the components (a) to (d). The range of ~ 100 parts by mass is most preferable. Within the above range, the effect of the tackifier can be exhibited while maintaining the adhesiveness, solder heat resistance and electrical characteristics.

<Filler>
If necessary, a filler such as silica may be added to the adhesive composition of the present invention. It is very preferable to add silica because the heat resistance property is improved. Hydrophobic silica and hydrophilic silica are generally known as silica, but here, hydrophobic silica treated with dimethyldichlorosilane, hexamethyldisilazane, octylsilane, etc. in order to impart moisture absorption resistance is used. Is good. When silica is blended, the blending amount is preferably 0.05 to 30 parts by mass with respect to a total of 100 parts by mass of the components (a) to (d). Further heat resistance can be exhibited by setting it to the above lower limit value or more. Further, by setting the value to the upper limit or less, it is possible to prevent poor dispersion of silica and excessively high solution viscosity, and workability is improved.

<Silane coupling agent>
A silane coupling agent may be added to the adhesive composition of the present invention, if necessary. It is very preferable to add a silane coupling agent because the properties of adhesion to metal and heat resistance are improved. The silane coupling agent is not particularly limited, and examples thereof include those having an unsaturated group, those having a glycidyl group, and those having an amino group. Of these, glycidyls such as γ-glycidoxypropyltrimethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, and β- (3,4-epoxycyclohexyl) ethyltriethoxysilane from the viewpoint of heat resistance. A silane coupling agent having a group is more preferable. When the silane coupling agent is blended, the blending amount thereof is preferably 0.5 to 20 parts by mass with respect to 100 parts by mass in total of the components (a) to (d). Within the above range, solder heat resistance and adhesiveness can be improved.

<Laminated body>
The laminate of the present invention is one in which an adhesive composition is laminated on a base material (two-layer laminate of a base material / adhesive layer), or one in which a base material is further bonded (base material / adhesive layer / It is a three-layer laminate of a base material). Here, the adhesive layer refers to a layer of the adhesive composition after the adhesive composition of the present invention is applied to a base material and dried. The laminate of the present invention can be obtained by applying and drying the adhesive composition of the present invention to various substrates according to a conventional method, and further laminating other substrates.

<Base material>
In the present invention, the base material is not particularly limited as long as the adhesive composition of the present invention can be applied and dried to form an adhesive layer, but the base material is a resin base material such as a film-like resin, or a metal. Examples include metal substrates such as plates and metal foils, papers, and the like.

Examples of the resin base material include polyester resin, polyamide resin, polyimide resin, polyamide-imide resin, liquid crystal polymer, polyphenylene sulfide, syndiotactic polystyrene, polyolefin resin, and fluorine resin. A film-like resin (hereinafter, also referred to as a base film layer) is preferable.

As the metal base material, any conventionally known conductive material that can be used for the circuit board can be used. Examples of the material include various metals such as SUS, copper, aluminum, iron, steel, zinc, and nickel, as well as alloys, plated products, and metals treated with other metals such as zinc and chromium compounds. A metal leaf is preferable, and a copper foil is more preferable. The thickness of the metal foil is not particularly limited, but is preferably 1 μm or more, more preferably 3 μm or more, and further preferably 10 μm or more. Further, it is preferably 50 μm or less, more preferably 30 μm or less, and further preferably 20 μm or less. If the thickness is too thin, it may be difficult to obtain sufficient electrical performance of the circuit, while if the thickness is too thick, the processing efficiency at the time of manufacturing the circuit may decrease. The metal leaf is usually provided in roll form. The form of the metal foil used in manufacturing the printed wiring board of the present invention is not particularly limited. When a ribbon-shaped metal foil is used, its length is not particularly limited. The width thereof is also not particularly limited, but is preferably about 250 to 500 cm. The surface roughness of the base material is not particularly limited, but is preferably 3 μm or less, more preferably 2 μm or less, and further preferably 1.5 μm or less. Further, it is practically preferably 0.3 μm or more, more preferably 0.5 μm or more, and further preferably 0.7 μm or more. Further, it is preferably 3 μm or less, more preferably 2 μm or less, and further preferably 1.5 μm or less.

Examples of papers include high-quality paper, kraft paper, roll paper, glassine paper, and the like. Further, as the composite material, glass epoxy or the like can be exemplified.

From the viewpoint of adhesive strength and durability with the adhesive composition, as the base material, polyester resin, polyamide resin, polyimide resin, polyamide-imide resin, liquid crystal polymer, polyphenylene sulfide, syndiotactic polystyrene, polyolefin resin, fluorine resin, etc. SUS steel plate, copper foil, aluminum foil, or glass epoxy is preferable.

<Adhesive sheet>
In the present invention, the adhesive sheet is a laminate of the laminate and a release base material via an adhesive composition. Specific configuration embodiments include a laminate / adhesive layer / release base material, or a release base material / adhesive layer / laminate / adhesive layer / release base material. By laminating the release base material, it functions as a protective layer of the base material. Further, by using the release base material, the release base material can be released from the adhesive sheet and the adhesive layer can be transferred to another base material.

The adhesive sheet of the present invention can be obtained by applying the adhesive composition of the present invention to various laminates and drying them according to a conventional method. In addition, if a release base material is attached to the adhesive layer after drying, it can be wound up without causing set-off to the base material, which is excellent in operability and protects the adhesive layer for storage stability. It is excellent and easy to use. Further, if the release base material is coated and dried, and then another release base material is attached as needed, the adhesive layer itself can be transferred to another base material.

<Release base material>
The release base material is not particularly limited, but for example, a coating layer of a sealant such as clay, polyethylene, or polypropylene is applied to both sides of paper such as high-quality paper, kraft paper, roll paper, and glassine paper. Examples thereof include those in which a silicone-based, fluorine-based, or alkyd-based mold release agent is coated on each of the coating layers. In addition, various olefin films such as polyethylene, polypropylene, ethylene-α-olefin copolymer, and propylene-α-olefin copolymer alone, and films such as polyethylene terephthalate coated with the above-mentioned release agent can also be mentioned. For reasons such as the release force between the release base material and the adhesive layer, and the fact that silicone adversely affects the electrical characteristics, polypropylene sealing treatment is applied to both sides of high-quality paper, and an alkyd-based release agent is used on top of it. Alternatively, it is preferable to use an alkyd-based mold release agent on polyethylene terephthalate.

The method for coating the adhesive composition on the substrate in the present invention is not particularly limited, and examples thereof include a comma coater and a reverse roll coater. Alternatively, if necessary, the adhesive layer may be provided directly or by a transfer method on the rolled copper foil or the polyimide film which is the constituent material of the printed wiring board. The thickness of the adhesive layer after drying is appropriately changed as needed, but is preferably in the range of 5 to 200 μm. Sufficient adhesive strength can be obtained by setting the adhesive film thickness to 5 μm or more. Further, when the thickness is 200 μm or less, it becomes easy to control the amount of residual solvent in the drying process, and blister is less likely to occur during pressing for manufacturing a printed wiring board. The drying conditions are not particularly limited, but the residual solvent ratio after drying is preferably 1% by mass or less. By setting the content to 1% by mass or less, foaming of the residual solvent during pressing of the printed wiring board is suppressed, and blistering is less likely to occur.

<Printed circuit board>
The "printed wiring board" in the present invention includes a laminate formed of a metal foil forming a conductor circuit and a resin base material as a constituent element. The printed wiring board is manufactured by a conventionally known method such as a subtractive method using a metal-clad laminate, for example. So-called flexible circuit boards (FPCs), flat cables, tape automated bonding (FPC), flat cables, tape automated bonding (FPC), flat cables, tape automated bonding, etc., in which a conductor circuit formed of metal foil is partially or completely coated with a cover film, screen printing ink, or the like, if necessary. It is a general term for circuit boards for TAB).

The printed wiring board of the present invention can have an arbitrary laminated structure that can be adopted as a printed wiring board. For example, it can be a printed wiring board composed of four layers, a base film layer, a metal foil layer, an adhesive layer, and a cover film layer. Further, for example, it can be a printed wiring board composed of five layers of a base film layer, an adhesive layer, a metal foil layer, an adhesive layer, and a cover film layer.

Further, if necessary, two or three or more of the above printed wiring boards may be laminated.

The adhesive composition of the present invention can be suitably used for each adhesive layer of the printed wiring board. In particular, when the adhesive composition of the present invention is used as an adhesive, it has high adhesiveness not only to the conventional polyimide, polyester film, and copper foil constituting the printed wiring board, but also to a low-polarity resin base material such as LCP. , Solder reflow resistance can be obtained, and the adhesive layer itself has excellent low dielectric properties. Therefore, it is suitable as an adhesive composition used for coverlay films, laminated boards, copper foils with resins, and bonding sheets.

In the printed wiring board of the present invention, any resin film conventionally used as the base material of the printed wiring board can be used as the base film. Examples of the resin of the base film include polyester resin, polyamide resin, polyimide resin, polyamide-imide resin, liquid crystal polymer, polyphenylene sulfide, syndiotactic polystyrene, polyolefin resin, and fluorine resin. In particular, it has excellent adhesiveness to low-polarity substrates such as liquid crystal polymers, polyphenylene sulfides, syndiotactic polystyrenes, and polyolefin resins.

<Cover film>
As the cover film, any conventionally known insulating film as an insulating film for a printed wiring board can be used. For example, films made from various polymers such as polyimide, polyester, polyphenylene sulfide, polyethersulfone, polyetheretherketone, aramid, polycarbonate, polyarylate, polyamideimide, liquid crystal polymer, syndiotactic polystyrene, and polyolefin resin are used. It is possible. More preferably, it is a polyimide film or a liquid crystal polymer film.

The printed wiring board of the present invention can be manufactured by any conventionally known process other than using the above-mentioned materials for each layer.

In a preferred embodiment, a semi-finished product in which an adhesive layer is laminated on a cover film layer (hereinafter, referred to as "cover film side semi-finished product") is manufactured. On the other hand, a semi-finished product (hereinafter referred to as "base film side two-layer semi-finished product") in which a metal foil layer is laminated on a base film layer to form a desired circuit pattern, or an adhesive layer is laminated on a base film layer. , A semi-finished product (hereinafter referred to as "base film side 3-layer semi-finished product") in which a metal foil layer is laminated on the metal foil layer to form a desired circuit pattern (hereinafter referred to as a base film-side 2-layer semi-finished product) Together with the base film side three-layer semi-finished product, it is called "base film side semi-finished product"). By laminating the cover film side semi-finished product thus obtained and the base film side semi-finished product, a four-layer or five-layer printed wiring board can be obtained.

The base film side semi-finished product is, for example, (A) a step of applying a resin solution to be a base film to the metal foil and initially drying the coating film, and (B) the metal foil obtained in (A). It is obtained by a production method including a step of heat-treating and drying the laminate with the initial dry coating film (hereinafter, referred to as "heat treatment / solvent removal step").

A conventionally known method can be used for forming the circuit in the metal foil layer. The active method may be used, or the subtractive method may be used. The subtractive method is preferable.

The obtained base film side semi-finished product may be used as it is for bonding with the cover film side semi-finished product, or for bonding with the cover film side semi-finished product after the release film is bonded and stored. You may use it.

The cover film side semi-finished product is manufactured by applying an adhesive to the cover film, for example. If necessary, a cross-linking reaction can be carried out on the applied adhesive. In a preferred embodiment, the adhesive layer is semi-cured.

The obtained cover film side semi-finished product may be used as it is for bonding with the base film side semi-finished product, or may be bonded to the base film side semi-finished product after the release film is bonded and stored. May be used for.

The base film side semi-finished product and the cover film side semi-finished product are, for example, stored in the form of rolls and then bonded together to manufacture a printed wiring board. Any method can be used as the bonding method, and for example, the bonding can be performed using a press or a roll. It is also possible to bond the two together while heating by a method such as using a heating press or a heating roll device.

In the case of a reinforcing material that can be wound up softly, for example, a polyimide film, the reinforcing material side semi-finished product is preferably manufactured by applying an adhesive to the reinforcing material. Further, in the case of a reinforcing plate that is hard and cannot be wound, such as a metal plate such as SUS or aluminum, or a plate obtained by curing glass fiber with epoxy resin, the adhesive previously applied to the release base material is transferred and applied. It is preferable to be manufactured. Further, if necessary, a cross-linking reaction can be carried out in the applied adhesive. In a preferred embodiment, the adhesive layer is semi-cured.

The obtained reinforcing material side semi-finished product may be used as it is for bonding with the back surface of the printed wiring board, or may be used for bonding with the base film side semi-finished product after the release film is bonded and stored. You may.

The base film side semi-finished product, the cover film side semi-finished product, and the reinforcing material side semi-finished product are all laminates for the printed wiring board in the present invention.

<Example>
Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the examples. In the examples and comparative examples, the term "part" simply indicates a part by mass.

(Physical property evaluation method)

Acid value (a) component: Acid-modified polyolefin The acid value (mgKOH / g) in the present invention was obtained by dissolving the acid-modified polyolefin in toluene and titrating with a methanol solution of sodium methoxydo using phenolphthalein as an indicator.

Number average molecular weight (Mn)
The number average molecular weight in the present invention is gel permeation chromatography manufactured by Shimadzu Corporation (hereinafter, GPC, standard substance: polystyrene resin, mobile phase: tetrahydrofuran, column: Shodex KF-802 + KF-804L + KF-806L, column. Temperature: 30 ° C., flow velocity: 1.0 ml / min, detector: RI detector).

Measurement of melting point and heat of melting The melting point and heat of melting in the present invention are increased at a rate of 20 ° C./min using a differential scanning calorimeter (hereinafter, DSC, manufactured by TA Instruments Japan, Q-2000). It is a value measured from the top temperature and area of the melting peak when the melting point is heated and melted again by hot melting and cooling resin conversion.

(1) Peeling strength (adhesiveness)
The adhesive composition described below was applied to a polyimide film having a thickness of 12.5 μm (manufactured by Kaneka Corporation, Apical (registered trademark)) so as to have a thickness of 25 μm after drying, and dried at 130 ° C. for 3 minutes. The adhesive film (B stage product) thus obtained was bonded to a rolled copper foil (manufactured by JX Nippon Mining & Metals Co., Ltd., BHY series) having a thickness of 18 μm. The bonding was performed by pressing the rolled copper foil under a pressure of 40 ^{kgf / cm 2} at 160 ° C. for 30 seconds so that the glossy surface of the rolled copper foil was in contact with the adhesive layer. Then, it was heat-treated at 140 ° C. for 4 hours to be cured to obtain a sample for evaluation of peel strength. The peel strength was measured by performing a 90 ° peel test at a film pulling rate of 50 mm / min at 25 ° C. This test shows the adhesive strength at room temperature. Samples were also prepared for a liquid crystal polymer (LCP) film (manufactured by Kuraray Co., Ltd., Vecstar CT-Z series, thickness 50 μm) and a syndiotactic polystyrene (SPS) film (thickness 100 μm).
<Evaluation criteria (PI film and LCP film)>
⊚: 1.0 N / mm or more ○: 0.8 N / mm or more and less than 1.0 N / mm Δ: 0.5 N / mm or more and less than 0.8 N / mm ×: 0.5 N / mm or less <Evaluation standard (SPS film) )>
⊚: 0.7 N / mm or more ○: 0.5 N / mm or more and less than 0.7 N / mm Δ: 0.3 N / mm or more and less than 0.5 N / mm ×: 0.3 N / mm or less

(2) Solder heat resistance A sample was prepared by the same method as above, and a 2.0 cm × 2.0 cm sample piece was aged at 23 ° C for 2 days and floated in a solder bath melted at 280 ° C for 10 seconds. It was confirmed whether there was any change in appearance such as swelling.
<Evaluation criteria>
⊚: No swelling ○: Partially swelling △: Many swelling ×: Swelling and discoloration

(3) Relative permittivity (ε _c ) and dielectric loss tangent (tan δ)
The adhesive composition described below was applied to a Teflon (registered trademark) sheet having a thickness of 100 μm so as to have a thickness of 25 μm after drying and curing, and dried at 130 ° C. for 3 minutes. Then, after heat-treating at 140 ° C. for 4 hours to cure, the Teflon (registered trademark) sheet was peeled off to obtain an adhesive resin sheet for testing. After that, the obtained test adhesive resin sheet was cut into strips of 8 cm × 3 mm to obtain a test sample. The relative permittivity (ε _c ) and the dielectric loss tangent (tan δ) were measured by a cavity resonator perturbation method using a network analyzer (manufactured by Anritsu) under the conditions of a temperature of 23 ° C. and a frequency of 1 GHz.
<Evaluation criteria for relative permittivity>
⊚: 2.3 or less ○: More than 2.3 and 2.6 or less Δ: More than 2.6 and 3.0 or less ×: More than 3.0 <Evaluation criteria for dielectric loss tangent>
⊚: 0.008 or less ○: 0.008 or more and 0.01 or less Δ: 0.01 or more and 0.02 or less ×: 0.02 or more

(4) Pot-life property Pot-life property is a solid content concentration of 20 mass of the components (a) to (d) and a mixed solvent of methylcyclohexane and toluene (methylcyclohexane / toluene = 80/20 (v / v)). A resin solution (varnish) is prepared by blending so as to be%, and refers to the stability of the varnish immediately after blending or after a certain period of time has passed after blending. If the pot life is good, it means that the viscosity of the varnish does not increase so much that it can be stored for a long time. If the pot life is poor, the viscosity of the varnish increases (thickening), and in severe cases, it means that the varnish can be stored for a long time. It means that a gelation phenomenon occurs, it becomes difficult to apply it to a base material, and it cannot be stored for a long period of time.
The varnish prepared according to the ratio shown in Table 1 was prepared using a Brookfield type viscometer to obtain a spindle type rotor No. 2. The viscosity of the dispersion liquid at 25 ° C. was measured at a rotation speed of 30 rpm to determine the initial dispersion liquid viscosity ηB0. Then, the varnish was stored at 25 ° C. for 7 days, and the dispersion viscosity ηB was measured at 25 ° C. The varnish viscosity was calculated by the following formula and evaluated as follows.
Solution viscosity ratio = solution viscosity ηB / solution viscosity ηB0
<Evaluation criteria>
⊚: 0.5 or more and less than 1.5 ○: 1.5 or more and less than 2.0 Δ: 2.0 or more and less than 3.0 ×: 3.0 or more or viscosity cannot be measured due to pudding

Example 1
80 parts by mass of acid-modified polyolefin CO-1, 20 parts by mass of phenol resin FTC-509 having a polycyclic structure, 10 parts by mass of epoxy resin HP-7200, and an organic solvent (methylcyclohexane / toluene = 80/20 (v). / V)) was blended in an amount of 440 parts by mass (20% by mass in terms of solid content concentration) to obtain an adhesive composition. Table 1 shows the blending amount, adhesive strength, solder heat resistance, and electrical characteristics.

Examples 2-18
The types and ratios of the resins used were changed as shown in Table 1, and Examples 2 to 18 were carried out in the same manner as in Example 1. Table 1 shows the adhesive strength, solder heat resistance, electrical properties and pot life properties. The organic solvent (methylcyclohexane / toluene = 80/20 (v / v)) was adjusted so that the solid content concentration was 20% by mass.

Comparative Examples 1 to 4
The types and ratios of the resins used were changed as shown in Table 1, and Comparative Examples 1 to 4 were carried out in the same manner as in Example 1. Table 1 shows the adhesive strength, solder heat resistance, electrical properties and pot life properties.

The acid-modified polyolefin (a), the phenol resin (b) having a polycyclic structure, and the epoxy resin (c) polycarbodiimide (d) used in Table 1 are as follows.
(Phenol resin (b) having a polycyclic structure)
Phenol resin (b1): FTC-509 (manufactured by Gun Ei Chemical Industry Co., Ltd.), a phenol resin having the structures of the general formula (2) and the general formula (11). Both x and y are 0, Z ₁ is 1, and the hydroxyl group is bonded to the para position of the benzyl group.
Phenol resin (b2): FATC-809 (manufactured by Gun Ei Chemical Industry Co., Ltd.), a phenol resin having the structures of the general formula (2) and the general formula (11). R ₃ and R ₄ are both 2-propenyl groups, x, y, and Z ₁ are both 1, and the hydroxyl group is bonded to the para position of the benzyl group.
Phenol resin (b3): FTC-809AE (manufactured by Gun Ei Chemical Industry Co., Ltd.), a phenol resin having the structures of the general formula (2) and the general formula (12). Both x and y are 0, Z ₁ and Z ₂ are both 1, and the ether group is bonded to the para position of the benzyl group.
Phenol resin (b4): YS Polystar T-100 (Phenol resin not containing a polycyclic structure manufactured by Yasuhara Chemical Co., Ltd.)
(Epoxy resin (c))
Dicyclopentadiene type epoxy resin: HP-7200 (DIC Epoxy equivalent 259 g / eq)
Dicyclopentadiene type epoxy resin: HP-7200H (DIC Epoxy equivalent 278 g / eq)
Cresol novolac type epoxy resin: jER-152 (Mitsubishi Chemical's epoxy equivalent 177g / eq)
Triglycidyl paraaminophenol: jER-630 (Mitsubishi Chemical Epoxy Equivalent 98g / eq)
(Polycarbodiimide (d))
Carbodiimide resin: V-09GB (Carbodiimide equivalent 216 g / eq manufactured by Nisshinbo Chemical Co., Ltd.)
Carbodiimide resin: V-03 (Carbodiimide equivalent 209 g / eq manufactured by Nisshinbo Chemical Co., Ltd.)

(Acid-modified polyolefin (a))
Manufacturing example 1
100 parts by mass of propylene-butene copolymer (“Toughmer (registered trademark) XM7080” manufactured by Mitsui Chemicals, Inc.), 150 parts by mass of toluene, 19 parts by mass of maleic anhydride, 6 parts by mass of di-tert-butyl peroxide in 1 L autoclave. Was added, the temperature was raised to 140 ° C., and the mixture was further stirred for 3 hours. Then, the obtained reaction solution was cooled and then poured into a container containing a large amount of methyl ethyl ketone to precipitate a resin. Then, the liquid containing the resin was centrifuged to separate and purify the acid-modified propylene-butene copolymer graft-polymerized with maleic anhydride, (poly) maleic anhydride and a low molecular weight substance. Then, by drying under reduced pressure at 70 ° C. for 5 hours, a maleic anhydride-modified propylene-butene copolymer (CO-1, acid value 19 mgKOH / g, number average molecular weight 25,000, Tm80 ° C., ΔH35J / g) Got

Manufacturing example 2
By carrying out the same procedure as in Production Example 1 except that the amount of maleic anhydride charged was changed to 14 parts by mass, the maleic anhydride-modified propylene-butene copolymer (CO-2, acid value 14 mgKOH / g, number average molecular weight 30) was used. 000, Tm78 ° C., ΔH25J / g) was obtained.

Manufacturing example 3
By carrying out the same procedure as in Production Example 1 except that the amount of maleic anhydride charged was changed to 11 parts by mass, the maleic anhydride-modified propylene-butene copolymer (CO-3, acid value 11 mgKOH / g, number average molecular weight 33) was used. 000, Tm 80 ° C., ΔH25J / g) was obtained.

Manufacturing example 4
By carrying out the same procedure as in Production Example 1 except that the amount of maleic anhydride charged was changed to 6 parts by mass, the maleic anhydride-modified propylene-butene copolymer (CO-4, acid value 7 mgKOH / g, number average molecular weight 35). 000, Tm 82 ° C., ΔH25J / g) was obtained.

As is clear from Table 1, in Examples 1 to 18, the pot life of the main agent was excellent, and as the adhesive, the resin base material (PI, LCP, SPS) and the copper foil had excellent adhesiveness and solder heat resistance. And has low dielectric properties. On the other hand, in Comparative Example 1, since the component (b) is not blended, the solder heat resistance is inferior. In Comparative Example 2, since the component (b) does not have a polycyclic structure, the low dielectric property (electrical property) is inferior. In Comparative Example 3, since the component (c) is not contained, the solder heat resistance is inferior. In Comparative Example 4, since the component (a) is not blended, the adhesive strength with each base material is poor and the low dielectric property is inferior.

The adhesive composition of the present invention has high adhesiveness not only to conventional polyimide and polyethylene terephthalate films but also to resin base materials such as LCP and SPS and metal base materials such as copper foil, and has high solder heat resistance. It is also excellent in pot life and low dielectric properties (electrical properties). The adhesive composition of the present invention can obtain an adhesive sheet and a laminate bonded using the adhesive sheet. Due to the above characteristics, it is useful for flexible printed wiring board applications, especially for FPC applications where low dielectric properties (low dielectric constant, low dielectric loss tangent) in a high frequency region are required.

Claims

An adhesive composition containing an acid-modified polyolefin (a), a phenol resin (b) having a polycyclic structure, and an epoxy resin (c).
The adhesive composition according to claim 1, wherein the phenol resin (b) having a polycyclic structure is a phenol resin having a tricyclodecane skeleton.
The adhesive composition according to claim 1 or 2, wherein the phenol resin (b) having a polycyclic structure is a phenol resin further having a carbonate skeleton.
The adhesive composition according to any one of claims 1 to 3, wherein the acid value of the acid-modified polyolefin (a) is 5 to 40 mgKOH / g.
The adhesive composition according to any one of claims 1 to 4, further containing polycarbodiimide (d).
A claim containing 0.05 to 120 parts by mass of a phenol resin (b) having a polycyclic structure and 0.1 to 60 parts by mass of an epoxy resin (c) with respect to 100 parts by mass of the acid-modified polyolefin (a). Item 2. The adhesive composition according to any one of Items 1 to 5.
The adhesive composition according to claim 5 or 6, which contains 0.1 to 30 parts by mass of polycarbodiimide (d) with respect to 100 parts by mass of the acid-modified polyolefin (a).
The adhesive composition according to any one of claims 1 to 7, wherein the relative permittivity (ε c ) at 1 GHz is 3.0 or less and the dielectric loss tangent (tan δ) is 0.02 or less.
An adhesive sheet containing the adhesive composition according to any one of claims 1 to 8.
A laminate containing the adhesive composition according to any one of claims 1 to 8.
A printed wiring board containing the laminate according to claim 10 as a component.