WO2017183497A1 - 硬化性組成物、該組成物を用いる硬化膜およびオーバーコート膜 - Google Patents
硬化性組成物、該組成物を用いる硬化膜およびオーバーコート膜 Download PDFInfo
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- WO2017183497A1 WO2017183497A1 PCT/JP2017/014630 JP2017014630W WO2017183497A1 WO 2017183497 A1 WO2017183497 A1 WO 2017183497A1 JP 2017014630 W JP2017014630 W JP 2017014630W WO 2017183497 A1 WO2017183497 A1 WO 2017183497A1
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- 0 CC(*(C)O*)c1ccc(C2(c(cccc3)c3-c3c2cccc3)c2ccc(*(C)*C(O)=*C)cc2)cc1 Chemical compound CC(*(C)O*)c1ccc(C2(c(cccc3)c3-c3c2cccc3)c2ccc(*(C)*C(O)=*C)cc2)cc1 0.000 description 2
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/83—Chemically modified polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/675—Low-molecular-weight compounds
- C08G18/6755—Unsaturated carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/44—Polycarbonates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/487—Polyethers containing cyclic groups
- C08G18/4879—Polyethers containing cyclic groups containing aromatic groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/06—Polyurethanes from polyesters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/08—Polyurethanes from polyethers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09D201/06—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
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- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/09—Use of materials for the conductive, e.g. metallic pattern
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- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/22—Secondary treatment of printed circuits
- H05K3/28—Applying non-metallic protective coatings
Definitions
- the present invention relates to a novel curable composition used for an electrically insulating protective film, a method for forming a protective film for a flexible wiring board using the composition, a flexible wiring board and an electronic component, and a method for producing the flexible wiring board.
- a novel curable composition used for an electrically insulating protective film, a method for forming a protective film for a flexible wiring board using the composition, a flexible wiring board and an electronic component, and a method for producing the flexible wiring board.
- resin compositions for example, sealants, solder resists, etc.
- resin compositions used for electronic parts have better heat resistance in order to cope with downsizing, thinning, and speeding up. It is required to have electrical properties and moisture resistance. Therefore, as a resin constituting the resin composition, a polyimide resin, a polyamideimide resin, or a polyamide resin has been used instead of an epoxy resin.
- these resins have a rigid resin structure and a cured film lacks flexibility. Therefore, when it uses for a thin film base material, there exists a problem that the base material after hardening is easy to warp largely, and is inferior in flexibility.
- Patent Document 4 discloses a thermosetting resin composition which is improved in low warpage, flexibility, solder heat resistance and tin plating resistance.
- the thermosetting resin composition of Patent Document 4 has excellent performance in electrical insulation characteristics that maintain high electrical characteristics under high temperature and high humidity.
- Patent Document 5 is derived from an alicyclic diol that has low warpage, flexibility, bending resistance, low warpage, flexibility, and electrical insulation characteristics under high temperature and high humidity.
- a thermosetting resin composition containing a polyamideimide-modified polyurethane resin containing a structural unit is disclosed.
- thermosetting resin composition does not completely satisfy the bending resistance desired in the market, and an electric insulating protective film having further higher bending resistance has been desired.
- JP 62-106960 A Japanese Patent Laid-Open No. 8-12763 Japanese Unexamined Patent Publication No. 7-196798 JP 2006-117922 A Japanese Patent Laying-Open No. 2015-147940
- the conventional resin composition with improved warpage and flexibility is easy to infiltrate water molecules under high temperature and high humidity, and maintains high electrical characteristics. It was difficult. In order to impart high electrical properties, it is considered effective to introduce a rigid component into the resin structure and to have a high glass transition temperature, but according to this technique, the substrate after curing tends to warp greatly, In addition, problems such as poor flexibility occur.
- thermosetting resin composition described in Patent Document 4 can be improved to some extent in terms of low warpage, flexibility, solder heat resistance and tin plating resistance, it can provide a protection function against wiring breakage. It was difficult. Moreover, although the thermosetting resin composition described in Patent Document 5 has a certain degree of bending resistance, it is still not sufficient.
- the main object is to provide a thermosetting resin composition.
- the present inventors have flexible a curable composition having a specific structure and a compound having an imide bond and / or an amide bond as an essential component.
- the warp of the flexible wiring board when the printed curable composition is cured is small, and the protective film containing a cured product of this curable composition has flexibility and long-term electrical insulation properties.
- the present invention has been completed by finding that it has an excellent effect of suppressing breakage of a large wiring when the flexible wiring board covered with the protective film is shaken.
- Component A a functional group having at least one structural unit represented by the following formula (A), having at least one of an imide bond and an amide bond, and reacting with a curing agent A compound having, A curable composition comprising (Component B) a curing agent and (Component C) an organic solvent.
- the wavy line indicates the binding site with another structure at the end of the structure.
- Component A is (raw material a) a trivalent and / or tetravalent polycarboxylic acid derivative having an acid anhydride group, (raw material b) at least of the following general formula (1) and general formula (2) It contains a compound obtained by reacting a polyol represented by 1 side, (raw material c) polyisocyanate, and (raw material d) using the following formula (A2) and / or (A3) as a raw material. [1] The curable composition according to any one of [3].
- R 1 s each independently represents an organic residue derived from a diol having 3 to 36 carbon atoms
- n R 2 s each independently represent an aromatic organic residue. Represents at least one selected from a group, an organic residue further having a substituent on the aromatic organic residue, and an organic residue derived from a dicarboxylic acid having 3 to 36 carbon atoms, and n is independently 1 to 60 Represents an integer.
- R 3 s each independently represents an organic residue derived from a diol having 3 to 36 carbon atoms.
- M independently represents an integer of 1 to 60.
- each p independently represents an integer of 1 to 10.
- (Component A) in the curable composition specified in [4] is made from (raw material a), (raw material b), (raw material c), and (raw material d) as raw materials. ), (Raw material b), (raw material c), and many compounds corresponding to the raw material (d) can react with each other. Moreover, the polymer obtained will also change if the compounding ratio and reaction conditions of each monomer are changed. Therefore, the structure of the component A obtained is extremely diverse, and it is difficult to define with a specific structure, it can be said that it is common technical knowledge of those skilled in the art. And if the structure cannot be specified, the characteristics cannot be specified.
- [4 ′] (Component A) is (raw material a) a trivalent and / or tetravalent polycarboxylic acid derivative having an acid anhydride group, (raw material b) of the following general formula (1) and general formula (2) It contains at least one polyol represented by (raw material c) polyisocyanate, and (raw material d) a reaction product comprising the following formula (A2) and / or (A3) as a raw material [1]
- the (component A) is a compound having the structural unit represented by the formula (A), having at least one of an imide bond and an amide bond, and further having a urethane bond.
- [6] The curable composition according to any one of [1] to [5], wherein the acid value of (Component A) is from 10 to 50 mgKOH / g.
- (Component B) comprises a compound having two or more epoxy groups per molecule.
- Component C is at least one organic solvent selected from the group consisting of ether solvents, ester solvents, ketone solvents, and aromatic hydrocarbon solvents
- Component D at least one fine particle selected from the group consisting of inorganic fine particles and organic fine particles.
- Any one of [1] to [9] wherein the total amount of the component (A) and the component (B) is 100 parts by mass, and the component (B) is included in an amount of 1 to 55 parts by mass.
- a cured film comprising a cured product of the curable composition according to any one of [1] to [11].
- An overcoat film for a flexible wiring board obtained by coating and curing.
- [14] A part of or all of the surface of the flexible wiring board in which wiring is formed on the flexible substrate is covered with the overcoat film described in [13].
- Flexible wiring board [15] The flexible wiring board according to [14], wherein the wiring is tin-plated copper wiring.
- a method for producing a flexible wiring board covered with an overcoat film comprising the following (Step 1) and (Step 3) and optionally (Step 2); (Process 1) A step of forming a printed film on the pattern by printing the curable composition according to any one of [1] to [11] on at least a part of the wiring pattern portion of the flexible wiring board (step 2) ) A step of evaporating a part or all of the solvent in the printed film by placing the printed film obtained in step 1 in an atmosphere of 40 to 100 ° C. (step 3) A step of curing the printed film obtained in step 1 or the printed film obtained in step 2 at 100 to 170 ° C. to form an overcoat film. [17] An electronic component having the cured film according to [12].
- the curable composition of the present invention By curing the curable composition of the present invention, a cured film excellent in low warpage, flexibility, and long-term insulation reliability can be obtained, and the flexible wiring board is shaken by coating the cured film as a protective film. In this case, the effect of suppressing wiring breakage can be increased.
- the present invention is a protective film made of a cured product of the curable composition, and a flexible wiring board covered with the protective film, and warping is sufficiently suppressed while maintaining high insulation reliability.
- a flexible wiring board having excellent flexibility can be provided.
- Curable composition (Component A) a compound having at least one structural unit represented by the following formula (A), having at least one of an imide bond and an amide bond, and having a functional group that reacts with a curing agent, A curable composition containing (Component B) a curing agent and (Component C) an organic solvent.
- a wavy line indicates a binding site with another structure at the end of the structure.
- Component A (Component A) which is an essential component of the curable composition of the present invention has a structural unit represented by the formula (A) and has an imide bond.
- (Component A) may further have a urethane bond (—O—C ( ⁇ O) —NH—). Furthermore, (Component A) has a functional group that reacts with the curing agent.
- Preferable functional groups that react with the curing agent include at least one functional group of a carboxyl group, a hydroxyl group, an acid anhydride group, an isocyanato group, an amide group, and an amino group. When it has an isocyanato group, the isocyanato group is preferably protected with a blocking agent. In addition, other groups may be protected with a blocking agent, and those that react with the block body removed are regarded as functional groups.
- the structural unit having at least one of an imide bond and an amide bond and having the structural unit represented by the formula (A) as an essential component shrinkage of the cured product when the curable composition is cured is reduced.
- the cured film itself has the effect of high flexibility and excellent bending resistance.
- the aromatic ring concentration of (Component A), which is an essential component of the curable composition of the present invention, is preferably 1.0 to 6.0 mmol / g, and most preferably 1.5 to 5.0 mmol / g. It is. When it is 6.0 mmol / g or less, both warpage and bending resistance can be achieved. Moreover, in the case of 1.0 mmol / g or more, sufficient bending resistance can be obtained.
- the aromatic ring concentration means the number (mmol) of aromatic rings per 1 g of the compound. The aromatic ring concentration can be calculated from the charging ratio.
- the number of aromatic rings is counted as 1 for the benzene ring as in the formula (51) as follows. Since the biphenyl structure as in formula (52) and the 9H-fluorene structure in formula (53) have two benzene rings, the number of aromatic rings is counted as two. A naphthalene structure like the formula (54) counts 2 as the number of aromatic rings. Similarly, the anthracene structure (formula (55)) and the phenanthrene structure (formula (56)) count the number of aromatic rings as 3. In the triphenylene structure (formula (77)) and the binaphthyl structure (formula (58)), the number of aromatic rings is counted as four.
- the number of ⁇ in the formulas (51 ′) to (58 ′) represents the number of aromatic rings in the formulas (51) to (58), respectively.
- Component A is represented by (raw material a) a trivalent and / or tetravalent polycarboxylic acid derivative having an acid anhydride group, (raw material b) represented by at least one of general formula (1) and general formula (2). And a reaction product using (polyol) (raw material c) polyisocyanate, (raw material d) formula (A2) and / or (A3) as a raw material.
- Component A can be synthesized, for example, by the following methods 1 to 3.
- Method 1 Method 1
- Method 2 Method 2
- R 1 s each independently represents an organic residue derived from a diol having 3 to 36 carbon atoms
- n R 2 s each independently represent an aromatic organic residue. Represents at least one selected from a group, an organic residue further having a substituent on the aromatic organic residue, and an organic residue derived from a dicarboxylic acid having 3 to 36 carbon atoms, and n is independently 1 to 60 Represents an integer.
- m + 1 R 3 's each independently represents an organic residue derived from a diol having 3 to 36 carbon atoms.
- M independently represents an integer of 1 to 60
- Raw material d A diol compound of formula (A2) and / or formula (A3)
- each q independently represents an integer of 1 to 10.
- Preferred q is an integer of 1 to 4, particularly preferably an integer of 1 to 2, and the average value of q is 1 to 4 are preferable, and 1 or 2 is more preferable.
- each p independently represents an integer of 1 to 10.
- Preferable p is an integer of 1 to 4, particularly preferably an integer of 1 to 2, and the average value of p is 1 to 4 are preferable, and 1 or 2 is more preferable.
- Method 2 (Raw material c) polyisocyanate and (raw material a) a trivalent and / or tetravalent polycarboxylic acid derivative having an acid anhydride group are reacted to have at least one of an imide bond and an amide bond, A polyisocyanate having an isocyanato group at the terminal is obtained, and this includes (raw material b) a polyol represented by at least one of the general formula (1) and general formula (2), and (raw material d) the formula (A2). And / or reacting with the diol compound represented by (A3).
- Method 1 In the synthesis method of Method 1, first, (raw material b) a polyol represented by at least one of the general formula (1) and general formula (2), and (raw material d) the formula (A2) and / or the formula ( The diol compound of A3) is reacted with (raw material c) polyisocyanate to synthesize a polyisocyanate compound having a urethane bond and an isocyanato group at the terminal (hereinafter referred to as “(A 1 -1) compound”). To do.
- R 1 are each independently an organic residue derived from a diol having 3 to 36 carbons.
- the organic residue derived from the diol is a divalent group in which two hydroxy groups are removed from the diol.
- diol having 3 to 36 carbons examples include 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1,3-propanediol, 1,5-propanediol, Pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,8-octanediol, 1,9-nonanediol, 2-methyl-1,8-octanediol, 1,9- Nonanediol, 1,10-decanediol, 1,12-dodecanediol, hydrogenated dimer (C36) diol, chain diols such as diethylene glycol and triethylene glycol, 5-membered ring diols such as 1,2-cyclopentanedimethanol, 1,3-cyclopentanedimethanol and bis (hydroxymethyl) tricyclo [5.2
- R 1 is preferably a divalent hydrocarbon group having 3 to 18 carbon atoms and a chain structure, and more preferably a divalent hydrocarbon group having 4 to 9 carbon atoms and a chain structure.
- the hydrocarbon group is particularly preferably a divalent hydrocarbon group having 4 to 6 carbon atoms and having a chain structure.
- preferred diols capable of deriving the organic residue of R 1 include, for example, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1, 3-propanediol, 1,5-pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,8-octanediol, 1,9-nonanediol, 2-methyl-1, Examples include 8-octanediol, 1,9-nonanediol, and 1,10-decanediol.
- More preferable diols include, for example, 1,4-butanediol, 2-methyl-1,3-propanediol, 1,5-pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,8-octanediol, 1,9-no Diols, 2-methyl-1,8-octanediol, 1,9-nonanediol, and particularly preferred diols include, for example, 1,4-butanediol, 2-methyl-1,3-propanediol.
- 1,5-pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, and most preferred diols include 1,6-hexanediol, 3-methyl-1, 5-pentanediol.
- n R 2 s are each independently an organic group derived from a divalent aromatic group, a divalent aromatic group having a substituent, or a dicarboxylic acid having 3 to 36 carbon atoms. It is at least one selected from residues.
- the divalent aromatic group constituting R 2 is preferably a phenylene group or a phenylene group having a substituent.
- the phenylene group include a 1,2-phenylene group, a 1,3-phenylene group, and a 1,4-phenylene group.
- the substituent of the phenylene group having a substituent include an alkyl group having 1 to 10 carbon atoms, specifically, a 3-methyl-1,2-phenylene group, a 4-methyl-1,2-phenylene group.
- residue of the C3-C36 dicarboxylic acid constituting R 2 include malonic acid, succinic acid, adipic acid, sebacic acid, dodecanedioic acid, eicosanedioic acid, dimer acid, maleic acid, phthalate Residues such as acid, isophthalic acid, malic acid and tartaric acid can be mentioned.
- R 2 of the dicarboxylic acid residue is exemplified by the same divalent hydrocarbon group as R 1 having a structure in which the terminal carboxy group is removed from these dicarboxylic acids.
- R 2 preferred as R 2 are 1,2-phenylene group, 1,3-phenylene group, 1,4-phenylene group, and phenylene group having an alkyl group as a substituent, and more preferably 1,2-phenylene group, 1,3-phenylene group and 1,4-phenylene group, particularly preferably 1,2-phenylene group and 1,3-phenylene group.
- R 1 when R 1 '1,2-phenylene group, R 2 is 1,6-hexanediol, 3-methyl-1,5-pentanediol
- R 2 is an organic residue derived from 3-methyl-1,5-pentanediol.
- N represents an integer from 1 to 60.
- Preferred n is an integer of 1 to 45, particularly preferably an integer of 1 to 30.
- the average value of n is preferably 3 to 11, and more preferably 5 to 10.
- diol having 3 to 36 carbons examples include 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1,3-propanediol, 1,5-propanediol, Pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,8-octanediol, 1,9-nonanediol, 2-methyl-1,8-octanediol, 1,9- Nonanediol, 1,10-decanediol, 1,12-dodecanediol, hydrogenated dimer (C36) diol, chain diols such as diethylene glycol and triethylene glycol, 5-membered ring diols such as 1,2-cyclopentanedimethanol, 1,3-cyclopentanedimethanol and bis (hydroxymethyl) tricyclo [5.2
- R 3 is preferably a divalent hydrocarbon group having 3 to 18 carbon atoms and a chain structure, and more preferably a divalent hydrocarbon group having 4 to 9 carbon atoms and a chain structure.
- the hydrocarbon group is particularly preferably a divalent hydrocarbon group having 4 to 6 carbon atoms and having a chain structure.
- preferable diols capable of deriving the organic residue of R 3 include, for example, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 2-methyl-1, 3-propanediol, 1,5-pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,8-octanediol, 1,9-nonanediol, 2-methyl-1, Examples include 8-octanediol, 1,9-nonanediol, and 1,10-decanediol.
- More preferable diols include, for example, 1,4-butanediol, 2-methyl-1,3-propanediol, 1,5-pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, 1,8-octanediol, 1,9-no Diols, 2-methyl-1,8-octanediol, 1,9-nonanediol, and particularly preferred diols include, for example, 1,4-butanediol, 2-methyl-1,3-propanediol.
- 1,5-pentanediol, 1,6-hexanediol, 3-methyl-1,5-pentanediol, and most preferred diols include 1,6-hexanediol, 3-methyl-1, 5-pentanediol.
- M represents an integer from 1 to 60.
- Preferred m is an integer of 1 to 45, particularly preferably an integer of 1 to 30, and an average value of m is preferably 3 to 11, more preferably 5 to 10.
- the number average molecular weight of the diols of the general formulas (1) and (2) is preferably 500 to 5000, more preferably 750 to 4000, and particularly preferably 1000 to 3000.
- the compounds represented by formula (A2) and / or (A3) used as (raw material d) are as described above.
- (raw material c) polyisocyanate to be reacted with (raw material b) and (raw material d) is used.
- (Raw material c) The polyisocyanate is not particularly limited as long as it is a compound having two or more isocyanato groups.
- polyisocyanate examples include 1,3-cyclohexane diisocyanate, 1,4-cyclohexane diisocyanate, isophorone diisocyanate, 4,4′-dicyclohexylmethane diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane, 1,4- Cycloaliphatic polyisocyanates such as biurets of bis (isocyanatomethyl) cyclohexane, norbornene diisocyanate and isophorone diisocyanate; Diphenylmethane-2,4'-diisocyanate, 3,2'-dimethyldiphenylmethane-2,4'-diisocyanate, 3,3'-dimethyldiphenylmethane-2,4'-diisocyanate, 4,2'-dimethyldiphenylmethane-2,4 '-Diisocyanate, 4,3'-dimethyldiphenylme
- polyisocyanates having an aromatic ring preferred are polyisocyanates having an aromatic ring, and more preferred are diphenylmethane-4,4'-diisocyanate, diphenylmethane-3,3'-diisocyanate, diphenylmethane-3,4 ' -Polyisocyanates having an aromatic ring such as diisocyanate and diphenyl ether-4,4'-diisocyanate, and most preferred is diphenylmethane-4,4'-diisocyanate.
- the isocyanato group may be stabilized with a blocking agent in order to avoid changes over time.
- a blocking agent include alcohols such as hydroxy acrylate, methanol, and butanone oxime, phenol, and oxime, but there is no particular limitation.
- the mixing ratio of the diol compound of (raw material d) and the polyol of (raw material b) is appropriately selected depending on the amount of the structural unit of formula A to be finally introduced. As described above, they are mixed in such an amount that the ring concentration is 1.0 to 6.0 mmol / g.
- the blending ratio of the (raw material c) with the polyisocyanate with respect to the total of the (raw material b) and the raw material (d) is appropriately adjusted according to the number average molecular weight of the compound (A 1 -1) to be produced.
- the terminal of the compound (A 1 -1) to be generated is an isocyanato group, it is necessary that the number of hydroxyl groups in (raw material b) and raw material (d) ⁇ the number of isocyanate groups in (raw material c).
- the ratio of the number of isocyanato groups to the number of hydroxyl groups is preferably adjusted to be 1.01 or more. It is preferable to adjust to 0.0 or less.
- the number average molecular weight of the (A 1 -1) compound having an isocyanato group at the terminal is preferably 500 to 30000, more preferably 1000 to 25000, and particularly preferably 1500 to 20000.
- (A 1 -1) compound having an isocyanato group at the terminal is reacted with (raw material a) a trivalent and / or tetravalent polycarboxylic acid derivative having an acid anhydride group, A compound having a urethane bond and an amide bond and / or an imide bond is produced.
- (raw material a) is a trivalent polycarboxylic acid derivative having an acid anhydride group, it has one set of acid anhydride and one carboxyl group.
- (raw material a) is a tetravalent polycarboxylic acid derivative having an acid anhydride group, it has two sets of acid anhydrides, or one set of acid anhydride groups and two carboxyl groups. .
- the carboxyl group may form a derivative by forming an ester bond with alcohol.
- the polycarboxylic acid derivative means a polycarboxylic acid having an acid anhydride group or a derivative such as a carboxylic acid ester thereof.
- R 4 represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, or a phenyl group.
- R 5 represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms or a phenyl group
- Y 1 represents —CH 2 —, —CO—, —SO 2 —, or —O—. Represents.
- R 4 and R 5 are preferably a hydrogen atom, and Y 1 is preferably —CO— or —O—.
- trimellitic anhydride is particularly preferable from the viewpoint of cost.
- the tetravalent polycarboxylic acid derivative which has an acid anhydride group For example, the tetracarboxylic dianhydride represented by following General formula (5) can be mentioned. These can be used alone or in combination of two or more.
- Y 2 represents a tetravalent organic group.
- the tetracarboxylic dianhydride represented by the formula (5) is not particularly limited.
- the tetracarboxylic dianhydride is ethylene glycol bis (trimellitic anhydride) (TMEG), 3,3 ', 4,4'-diphenyltetracarboxylic dianhydride (BPDA), pyromellitic dianhydride.
- TMEG ethylene glycol bis (trimellitic anhydride)
- BPDA 4,4'-diphenyltetracarboxylic dianhydride
- PMDA 3,3 ′, 4,4′-benzophenone tetracarboxylic dianhydride
- ODPA 4,4′-oxydiphthalic dianhydride
- tetracarboxylic dianhydrides may be used alone or in combination of two or more.
- the mixing ratio of the (A′-1) compound having an isocyanato group at the terminal and the (raw material a) is within a range in which the finally produced compound has a urethane bond and an amide bond and / or an imide bond. There is no particular limitation.
- (A 1 -1) compound (A 1 -1) than the compounds of polyisocyanate (hereinafter, (A 1 -2) described as Compound.) Is reacted with with the (raw material a)
- a compound having a urethane bond and an amide bond and / or an imide bond may be obtained.
- the (A 1 -2) compound is not particularly limited as long as it is a polyisocyanate other than the (A 1 -1) compound, and examples thereof include the (raw material c). These can be used individually by 1 type or in combination of 2 or more types.
- the ratio of the total number of isocyanate groups of the combined isocyanate groups of isocyanate group and A 1 in -2 in A 1 -1 is not particularly limited, The range is preferably 0.9: 1.0 to 1.1: 1.0, and more preferably 0.95: 1.0 to 1.05: 1.0.
- an amine compound can be used in combination with the polyisocyanate.
- an amine compound the compound which converted the isocyanato group in the said polyisocyanate conversion into the amino group is mentioned. Conversion of the isocyanato group to an amino group can be performed by a known method.
- the aromatic polyisocyanate is particularly preferably 4,4′-diphenylmethane diisocyanate in consideration of the balance of solubility, mechanical properties and cost.
- (Method 2) In the synthesis method of (Method 2), first, (raw material c) polyisocyanate and (raw material a) a trivalent and / or tetravalent polycarboxylic acid derivative acid having an acid anhydride group are reacted to form an imide bond and A polyisocyanate having at least one amide bond (hereinafter referred to as “(A 2 ⁇ 1)” compound) is synthesized.
- (Raw material b) polyol represented by at least one of the above general formula (1) and general formula (2) and (raw material d) diol compound represented by the above formula (A2) and / or (A3) Is reacted.
- the blending ratio of (raw material c) polyisocyanate and (raw material a) trivalent and / or tetravalent polycarboxylic acid derivative acid having an acid anhydride group is the number average molecular weight of the compound (A 2 -1) to be produced. Depending on how much is adjusted, it is adjusted appropriately. However, since the terminal of the resulting (A 2 -1) compound is an isocyanato group, the total number of the acid anhydride groups and the number of carboxyl groups in (raw material a) ⁇ the total number of isocyanato groups in (raw material c) There is a need.
- R 3 and R 4 are hydrogen atoms, such as —COOR 3 in the compound represented by the formula (3) and —COOR 4 in the compound represented by the formula (4). Also includes the number of carboxyl groups.
- the ratio of the number of isocyanato groups, the number of acid anhydride groups, and the total number of carboxyl groups is preferably adjusted to be 1.01 or more, and is preferably adjusted to 2.0 or less.
- the number average molecular weight of the (A 2 -1) compound having an isocyanato group at the terminal is preferably 500 to 15000, more preferably 800 to 10,000, and particularly preferably 1,000 to 5,000.
- a compound having an urethane bond and an amide bond and / or an imide bond is produced by reacting the (A 2 -1) compound having an isocyanato group at the terminal with (raw material b) and (raw material d). Let The blending ratio of the (A 2 -1) compound to (raw material b) and (raw material d) is selected according to the final compound acid value and target molecular weight.
- the total number of isocyanate groups in A 2 -1, number of hydroxyl groups in the starting material b, and 2,2 number of hydroxyl groups in the polyol having a carboxyl group such as dimethylol propionic acid and 2,2-dimethylol butanoic acid is not particularly limited, but in the case of having an amide group in A 2 -1, it may be in the range of 0.9: 1.0 to 1.1: 1.0. More preferably, it is in the range of 0.95: 1.0 to 1.05: 1.0.
- raw materials b) and (d) used in the synthesis method of (Method 2) can be the same as (raw materials b) and (d) described in (Method 1) above.
- a polyol may be further added to form a urethane bond by a reaction between the terminal isocyanate group and the added polyol.
- (Method 3) In the synthesis method of (Method 3), first, (raw material c) polyisocyanate and (raw material a) trivalent and / or tetravalent polycarboxylic acid derivative acid having an acid anhydride group are reacted to form an imide bond and A compound having at least one amide bond and having an acid anhydride group and / or a carboxyl group at the terminal (hereinafter referred to as “(A 3 -1) compound”) is synthesized.
- the blending ratio of (raw material c) and (raw material a) is appropriately adjusted depending on how much the number average molecular weight of the (A 3 -1) compound to be produced is. However, since the terminal of the generated (A 3 -1) compound is an acid anhydride group and / or a carboxyl group, the total number of the acid anhydride group and the number of carboxyl groups in (raw material a)> (raw material c) the number of isocyanate groups.
- the ratio between the total number of acid anhydride groups and the number of carboxyl groups and the number of isocyanate groups is preferably adjusted to be 1.01 or more, and is preferably adjusted to 2.0 or less.
- the number average molecular weight of the (A 3 -1) compound having an acid anhydride group and / or a carboxyl group at the terminal is preferably 500 to 15000, more preferably 800 to 10,000, and more preferably 1000 to 5000. It is particularly preferred.
- the ratio of the total number of acid anhydride groups in A 3 -1 to the number of hydroxyl groups in raw material b is not particularly limited, but should be in the range of 0.9: 1.0 to 1.1: 1.0. More preferably, it is in the range of 0.95: 1.0 to 1.05: 1.0.
- the (raw material a) to (raw material d) used in the synthesis method of (Method 3) are the same as the (raw material a) to (raw material d) used in the synthesis method of (Method 1). be able to.
- the reaction of each raw material of these (Method 1) to (Method 3) can be performed by heating them in the presence of an organic solvent, preferably a non-nitrogen-containing polar solvent.
- organic solvent preferably a non-nitrogen-containing polar solvent.
- the non-nitrogen-containing polar solvent include ether solvents such as diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, and triethylene glycol diethyl ether; sulfur-containing solvents such as dimethyl sulfoxide, diethyl sulfoxide, dimethyl sulfone, and sulfolane.
- An ester solvent such as ⁇ -butyrolactone and cellosolve acetate; a ketone solvent such as cyclohexanone and methyl ethyl ketone; and an aromatic hydrocarbon solvent such as toluene and xylene. These can be used alone or in combination of two or more.
- solvents it is preferable to select and use a solvent that can dissolve the resin to be produced. Moreover, it is preferable to use what is suitable as a solvent of a thermosetting composition as it is after a synthesis
- ⁇ -butyrolactone and a mixed solvent containing ⁇ -butyrolactone are preferable in order to perform the reaction in a homogeneous system efficiently.
- the amount of solvent used is 100 parts by mass of the total amount of raw materials for synthesizing the compounds (A′-1), (B′-1), and (C′-1), respectively. 80 to 500 parts by mass is preferable.
- the amount used is 80 to 500 parts by mass with respect to 100 parts by mass of the total amount of raw materials, the viscosity at the time of synthesis does not become too high, the synthesis is not difficult due to the inability to stir, and the reaction rate is extremely high. It is preferable without being lowered.
- the reaction temperature is preferably 70 to 210 ° C., more preferably 75 to 190 ° C., and particularly preferably 80 to 180 ° C. If this temperature is less than 70 ° C, the reaction time tends to be too long, and if it exceeds 210 ° C, gelation tends to occur during the reaction.
- the reaction time can be appropriately selected depending on the capacity of the reaction vessel and the reaction conditions employed.
- the reaction may be performed in the presence of a catalyst such as a tertiary amine, an alkali metal, an alkaline earth metal, a metal such as tin, zinc, titanium, cobalt, or a metalloid compound.
- a catalyst such as a tertiary amine, an alkali metal, an alkaline earth metal, a metal such as tin, zinc, titanium, cobalt, or a metalloid compound.
- a catalyst such as a tertiary amine, an alkali metal, an alkaline earth metal, a metal such as tin, zinc, titanium, cobalt, or a metalloid compound.
- DBU 1,8-diazabicyclo [5.4.0] -7-undecene
- 4-dimethylaminopyridine 4-dimethylaminopyridine and the like are used, but the catalyst is not necessarily used.
- the raw material (c) polyisocyanate reacts the products (A) and (B) with (raw material a), the products (C) and (D), (raw material b) polyol and (raw material d). At this time, it may be added again according to the purpose such as molecular weight adjustment or acid value adjustment.
- the number average molecular weight means a value measured by gel permeation chromatography (GPC) and converted using a standard polystyrene calibration curve.
- GPC gel permeation chromatography
- the number average molecular weight, mass average molecular weight, and degree of dispersion are defined as follows.
- the measurement conditions of GPC are as follows.
- Device name HPLC unit HSS-2000 manufactured by JASCO Corporation
- Mobile phase Tetrahydrofuran Flow rate: 1.0 mL / min
- Detector JASCO Corporation RI-2031Plus Temperature: 40.0 ° C
- Sample amount 100 ⁇ l of sample loop Sample concentration: adjusted to around 0.1% by mass.
- the acid value of (Component A) is preferably 10 to 50 mgKOH / g. Further, it is preferably 10 to 35 mg KOH / g, and particularly preferably 15 to 30 mg KOH / g.
- the acid value can be adjusted by adjusting the amount of carboxyl groups generated by the reaction.
- A represents the acid value (mgKOH / g)
- Vf represents the titration amount (mL) of the 0.1N KOH solution
- Wp represents the mass (g) of the solution containing (Component A).
- I represents the proportion (% by mass) of the nonvolatile content of the solution containing (Component A).
- the number average molecular weight of the component A thus obtained is preferably 5000 to 65000, more preferably 6000 to 40000, and particularly preferably 7000 to 25000.
- a number average molecular weight of 5,000 to 65,000 is preferred because it can suppress a decrease in weather resistance or chemical resistance and can maintain solubility in a non-nitrogen-containing polar solvent.
- the curable composition which concerns on this embodiment further contains the hardening
- the curing agent is a compound having two or more functional groups capable of reacting with the functional group of the component (A) in one molecule.
- the curing agent of the component (B) is an epoxy group or isocyanato that reacts with those functional groups. It preferably has a plurality of groups, hydroxyl groups and carboxyl groups.
- Examples of the epoxy group-containing compound used as a curing agent include one or more compounds having one or more epoxy groups in one molecule, and further include compounds having two or more epoxy groups in one molecule. Those are preferred.
- a compound having two or more epoxy groups in one molecule when included, it may be used alone, and together with a compound having two or more epoxy groups in the molecule, one epoxy group in the molecule. The compound which has this may contain.
- epoxy group-containing compound used as the curing agent examples include phenol novolac type epoxy resins, orthocresol novolak type epoxy resins, phenol, cresol, xylenol, resorcin, catechol, phenols and / or ⁇ -naphthol.
- Diglycidy such as novolak epoxy resin, bisphenol A, bisphenol F, bisphenol S, alkyl-substituted or unsubstituted biphenol, stilbene phenols Luether (bisphenol A type epoxy compound, bisphenol F type epoxy compound, bisphenol S type epoxy compound, biphenyl type epoxy compound, stilbene type epoxy compound), glycidyl ether of alcohols such as butanediol, polyethylene glycol, polypropylene glycol, phthalic acid, Glycidyl type such as glycidyl ester type epoxy resin of carboxylic acids such as isophthalic acid
- methyl glycidyl type epoxy resin, active hydrogen bonded to nitrogen atom of aminophenols such as p-aminophenol and active hydrogen of phenolic hydroxyl group are replaced with glycidyl group Glycidyl type or methyl glycidyl type epoxy resin, vinylcyclohexene diepoxide obtained by epoxidizing the olefin bond in the molecule, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, 2- ( 3,4-epoxy) cyclohexyl-5,5-spiro (3,4-epoxy) cyclohexane-m-dioxane and other alicyclic epoxy resins, paraxylylene and / or metaxylylene modified glycidyl ethers, terpene modified phenolic resins Glycidyl ether, glycidyl ether of dicyclopentadiene modified
- a compound having two or more epoxy groups in one molecule and having an aromatic ring structure and / or an alicyclic structure is preferable.
- cyclopentadiene-modified phenolic resins of glycidyl ether i.e., tricyclo [5,2,1,0 2,6] have decane structure and aromatic ring structure and a compound having two or more epoxy groups
- 1,3-bis (1-adamantyl) -4,6-bis (glycidylyl) benzene 1- [2 ′, 4′-bis (glycidylyl) phenyl] adamantane, 1,3-bis (4′-glycidylylphenyl) adamantane and 1
- Component A when importance is attached to the reactivity with the aforementioned (Component A) of the present invention, among compounds having two or more epoxy groups in one molecule and having an aromatic ring structure and / or an alicyclic structure.
- glycidyl type or methyl glycidyl type epoxy resins such as those in which active hydrogen bonded to the nitrogen atom of aniline or bis (4-aminophenyl) methane is substituted with a glycidyl group, nitrogen of aminophenols such as p-aminophenol
- An amino group and an aromatic ring structure such as an active hydrogen bonded to an atom and an active hydrogen of a phenolic hydroxyl group substituted with a glycidyl group or an epoxy resin of a methyl glycidyl type, and two or more epoxy groups
- the compound which has is preferable, Especially preferably, it is a compound as described in following formula (7).
- examples of the compound having a plurality of isocyanates used as a curing agent that is, a polyisocyanate compound include diisocyanate compounds, triisocyanates, and other tetrafunctional or higher functional isocyanates.
- a blocked polyisocyanate compound in which an isocyanato group is stabilized with a blocking agent can be used individually by 1 type or in combination of 2 or more types.
- the blocking agent includes alcohol, phenol, oxime, etc., but is not particularly limited.
- this blocked isocyanate for example, trade names “DURANATE 17B-60PX, TPA-B80E, MF-B60X, MF-K60X, E402-B80T” manufactured by Asahi Kasei Chemicals Corporation, trade names “Karenz MOI-BM, MOI-BP ”, trade names“ BL-3175, BL-4165, Desmo Cup 11, Desmo Cup-12 ”manufactured by Sumika Bayer Urethane Co., Ltd., and the like.
- the blocked isocyanate is preferably selected in accordance with the thermosetting temperature of (Component A), and BL-3175 is particularly preferable for low temperature curing.
- the hydroxyl group-containing compound used as the curing agent is one or more compounds having a hydroxyl group in one molecule, and at least one of them contains a compound having two or more hydroxyl groups in one molecule. There is no particular limitation.
- hydroxyl group-containing compound used as the curing agent examples include polyhydric alcohols, and specific examples include ethylene glycol, glycerin, butanediol, pentaerythritol and the like.
- the carboxyl group-containing compound used as the curing agent is one or more compounds having a carboxyl group in one molecule, and at least one of them has a compound having two or more carboxyl groups in one molecule. If included, there is no particular limitation.
- carboxyl group-containing compound used as the curing agent examples include polyvalent carboxylic acids, and specific examples include phthalic acid, succinic acid, trimellitic acid, adipic acid, pyromellitic acid and the like.
- an epoxy group-containing compound, a polyisocyanate compound, a hydroxyl group-containing compound, and a carboxyl group-containing compound can be used alone or in combination, and can be selected according to the reactive group of (Component A).
- (Component A) has a hydroxy group
- (Component A) has a carboxyl group or an amino group
- an epoxy-containing compound is not limited to an epoxy group-containing compound, a polyisocyanate compound, a hydroxyl group-containing compound, and a carboxyl group-containing compound as long as it reacts with the reactive group of (Component A).
- the amount of (Component B) in the curable composition of the present invention is 1 to 55% by mass, preferably 2 to 45% by mass, based on the total amount of (Component A) and (Component B) in the curable composition. More preferably, it is 2.5 to 30% by mass.
- the amount of (Component B) in the curable composition of the present invention is 1 to 55% by mass based on the total mass of (Component A) and (Component B) in the curable composition. It is preferable from the viewpoint of the solvent resistance of the cured film, and is balanced with the low warpage property of the flexible wiring board characterized by being covered with the cured film, suitable electrical insulation reliability, and the effect of suppressing the wiring breakage. be able to.
- the amount of (Component A) in the curable composition of the present invention is 45 to 99% by mass, preferably 55 to 98%, based on the total amount of (Component A) and (Component B) in the curable composition. % By mass, more preferably 70 to 97.5% by mass.
- the amount of (Component A) in the curable composition of the present invention is 45 to 99% by mass based on the total amount of (Component A) and (Component (B) in the curable composition. It is preferable from the viewpoint of the solvent resistance of the cured film of the invention, and it is possible to balance the low warpage of the flexible wiring board characterized by being covered with the cured film and the suppression hardening of the wiring breakage.
- component C which is an essential component of the curable composition of the present invention.
- the organic solvent used as component C is not particularly limited as long as it can dissolve (component A) and (component B). Examples thereof include diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol ethyl methyl ether, and diethylene glycol diester.
- Ether solvents such as butyl ether, diethylene glycol butyl methyl ether, diethylene glycol isopropyl methyl ether, triethylene glycol dimethyl ether, triethylene glycol butyl methyl ether, tetraethylene glycol dimethyl ether, dipropylene glycol dimethyl ether, tripropylene glycol dimethyl ether, ethylene glycol monomethyl ether Acetate, ethylene glycol monoethyl Ether acetate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, dipropylene glycol monomethyl ether acetate, dipropylene glycol monoethyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol monomethyl ether acetate, methyl methoxypropionate, methoxypropionic acid Ester solvents such as ethyl, methyl ethoxypropionate, ethyl ethoxyprop
- ⁇ -butyrolactone, diethylene glycol diethyl ether, diethylene glycol monoethyl ether acetate, and diethylene glycol monomethyl ether acetate are preferable, and ⁇ -butyrolactone and diethylene glycol are more preferable in consideration of the balance between screen printability and organic solvent volatility.
- These preferable solvent combinations are suitable because they are excellent as solvents for screen printing ink.
- the content of (Component C) in the curable composition of the present invention is (Component A), (Component B), (Component C), and (Component D) described later, which are components of the curable composition of the present invention.
- the total amount is preferably 25 to 75 parts by mass, more preferably 35 to 65 parts by mass.
- the total amount of (Component A), (Component B) and (Component C)) is 25 to 75 parts by weight of the curable composition. Since the viscosity is good for printing by the screen printing method and the spread due to bleeding of the curable composition after screen printing does not increase so much, as a result, the portion to be coated with the curable composition (that is, the shape of the printing plate) ), The printing area of the actual curable composition does not become too large.
- (Component C) is preferably contained in an amount of 0.5 to 20 parts by mass with respect to 100 parts by mass of (Component A). Moreover, it is preferable that the curable composition of this invention contains the at least 1 sort (s) of microparticles
- inorganic fine particles examples include silica (SiO 2 ), alumina (Al 2 O 3 ), titania (TiO 2 ), tantalum oxide (Ta 2 O 5 ), zirconia (ZrO 2 ), silicon nitride (Si 3 N 4 ).
- the organic fine particles are preferably heat-resistant resin fine particles having an amide bond, an imide bond, an ester bond or an ether bond.
- These resins are preferably polyimide resins or precursors thereof, polyamideimide resins or precursors thereof, or polyamide resins from the viewpoint of heat resistance and mechanical properties. These can be used alone or in combination of two or more.
- (Component D) includes at least one selected from silica fine particles and hydrotalcite fine particles.
- the silica fine particles used in the curable composition of the present invention are defined to include fine particles that are powdery, physically coated or chemically surface-treated with an organic compound.
- the silica particles used in the curable composition of the present invention are not particularly limited as long as they are dispersed in the curable composition of the present invention to form a paste.
- Silica fine particles represented by these aerosils are sometimes used for imparting printability during screen printing, and in that case, they are used for the purpose of imparting thixotropy.
- hydrotalcite is a kind of naturally occurring clay minerals typified by Mg 6 Al 2 (OH) 16 CO 3 .4H 2 O and is a layered inorganic compound.
- the hydrotalcite may be a synthetic material, and such a hydrotalcite is an Mg / Al-based layered compound, and chloride ions (Cl ⁇ ) and ion are exchanged with a carbonate group between layers. / Or Anion of sulfate ion (SO 4 ⁇ ) can be immobilized. Using this function, chloride ions (Cl ⁇ ) and sulfate ions (SO 4 ⁇ ), which cause migration of copper and tin, can be captured and used for the purpose of improving insulation reliability. .
- Examples of commercial products of hydrotalcite include STABIACE HT-1, STABIACE HT-7, and STABIACE HT-P from Sakai Chemical Co., Ltd., DHT-4A, DHT-4A2, and DHT-4C from Kyowa Chemical Industry Co., Ltd. Is mentioned.
- the average particle diameter of these inorganic fine particles and / or organic fine particles is preferably 0.01 to 10 ⁇ m, more preferably 0.1 to 5 ⁇ m.
- the blending amount of (Component D) is 0.1 to 60% by mass, preferably 0.3 to 4%, based on the total amount of (Component A), (Component B), (Component C) and (Component D).
- the content is 55% by mass, and more preferably 0.5 to 40% by mass.
- the curable composition Since the viscosity of the product is good for printing by the screen printing method and the spread due to bleeding of the curable composition after screen printing does not increase so much, as a result, the portion where the curable composition is to be applied (that is, the printing plate) The actual printed area of the curable composition does not become too large.
- (Component D) is preferably contained in an amount of 1 to 30 parts by mass with respect to 100 parts by mass of (Component A).
- a method of dispersing Component D
- roll kneading, mixer mixing, etc. which are usually performed in the paint field, are applied, and any method can be used that sufficiently disperses.
- the curable composition of the present invention can and preferably includes an antifoaming agent for the purpose of eliminating or suppressing the generation of bubbles during printing.
- antifoaming agent used in the curable composition of the present invention include, for example, BYK-077 (manufactured by Big Chemie Japan), SN deformer 470 (manufactured by San Nopco), TSA750S (momentive performance Materials), silicone oil SH-203 (manufactured by Toray Dow Corning), Dappo SN-348 (San Nopco), Dappo SN-354 (San Nopco), Acrylic polymer antifoaming agents such as Dappo SN-368 (manufactured by San Nopco), Disparon 230HF (manufactured by Enomoto Kasei Co., Ltd.), Surfynol DF-110D (manufactured by Nissin Chemical Industry Co., Ltd.), Surfynol DF-37 ( Acetylenic diol antifoaming agents such as Nissin Chemical Industry Co., Ltd. And the like fluorine-containing silicone-based defo
- the content of the antifoaming agent is the total amount of (Component A), (Component B), (Component C) and (Component D) (provided that (Component D) is not included in the curable composition of the present invention).
- the antifoaming agent is preferably contained in an amount of 0.2 to 10 parts by mass with respect to 100 parts by mass of (Component A).
- the curable composition of the present invention can and preferably includes a curing accelerator.
- the curing accelerator is not particularly limited as long as it is a compound that accelerates the reaction between an epoxy group and a carboxyl group.
- melamine, acetoguanamine, benzoguanamine, 2,4-diamino-6-methacryloyloxyethyl-S Triazines such as triazine, 2,4-methacryloyloxyethyl-s-triazine, 2,4-diamino-6-vinyl-s-triazine, 2,4-diamino-6-vinyl-s-triazine and isocyanuric acid adducts
- imidazole 2-methylimidazole, 2-ethyl-4-methylimidazole, 2-phenylimidazole, 2-undecylimidazole, 2-heptadecylimidazole, 1-benzyl-2-methylimidazole, 2-phenyl-4-methylimidazole 1-cyanoethyl-2 Methylimidazole, 1-cyanoethyl-2-ethyl-4-methylimidazole, 1-amino
- curing accelerators may be used alone or in combination of two or more.
- preferred curing accelerators in view of achieving both curing acceleration and electrical insulation performance, preferred are melamine, imidazole compounds, cycloamidine compounds, derivatives of cycloamidine compounds, phosphine compounds and amines. More preferred are melamine, 1,5-diazabicyclo (4.3.0) nonene-5 and salts thereof, and 1,8-diazabicyclo (5.4.0) undecene-7 and salts thereof.
- the blending amount of these curing accelerators is not particularly limited as long as the curing acceleration effect can be achieved.
- the curable composition of the present invention contains It is preferably blended in the range of 0.05 to 5 parts by mass, more preferably 0.1 to 3 parts by mass with respect to 100 parts by mass of the total amount of (Component A) and (Component B) as essential components of the present invention Part.
- the blending amount is in the range of 0.05 to 5 parts by mass with respect to 100 parts by mass of the total amount of (Component A) and (Component B), it can be cured in a short time and the curability of the present invention.
- the electrical insulation characteristics and water resistance of the overcoat film obtained by curing the composition are improved.
- the curable composition of the present invention includes a phenolic antioxidant, a phosphite antioxidant, a thioether antioxidant, and the like.
- An antioxidant can be added.
- a leveling agent a colorant such as a dye or a pigment, a flame retardant, and a lubricant are added to the curable composition of the present invention in order to improve workability during coating and film properties before and after film formation. You can also.
- the method for producing the curable composition of the present invention is not particularly limited as long as (Component A), (Component B) and (Component C) and, if necessary, other components can be dissolved or dispersed in an organic solvent.
- the curable composition of the present invention may be produced by producing a main agent containing at least (Component A) and a curing agent containing at least (Component B), and then blending the main agent and the curing agent. .
- the curable composition of the present invention improves screen printability and prevents the composition from flowing and not having a constant film thickness after printing the curable composition.
- the thixotropy index is desirably 1.1 or more at 25 ° C., more preferably in the range of 1.1 to 3.0, and particularly preferably in the range of 1.1 to 2.5.
- there are a method of adjusting the thixotropy index using the inorganic fine particles and organic fine particles there are a method of adjusting the thixotropy index using a polymer additive, and the like. The method of adjusting the thixotropy index using inorganic fine particles or organic fine particles is preferred.
- the “thixotropic index” described in this specification is a rotation at 25 ° C. measured using a cone / plate viscometer (manufactured by Brookfield, model: DV-II + Pro, spindle model number: CPE-52). It is defined as the ratio of the viscosity at several rpm and the viscosity at 10 rpm at 25 ° C.
- the curable composition of the present invention includes a phenolic antioxidant, a phosphite antioxidant, a thioether antioxidant, and the like.
- An antioxidant can be added.
- a leveling agent a colorant such as a dye or a pigment, a flame retardant, and a lubricant are added to the curable composition of the present invention in order to improve workability during coating and film properties before and after film formation. You can also.
- the curable composition preferably has a viscosity at 25 ° C. of 20 Pa ⁇ s to 80 Pa ⁇ s, more preferably 30 Pa ⁇ s to 50 Pa ⁇ s, as measured by a rotary viscometer.
- a viscosity is less than 20 Pa ⁇ s, there is a tendency that the flow of the composition after printing becomes large and the film thickness tends to be reduced, and when it exceeds 80 Pa ⁇ s, the transfer property of the composition to the substrate is increased. There is a tendency that voids and pinholes in the printed film increase with decreasing.
- the cured film of the present invention includes a cured product that can be obtained by curing the curable composition of the present invention.
- the electronic component of the present invention has the cured film.
- the overcoat film of the present invention is an overcoat film for a flexible wiring board containing a cured product of the curable composition of the present invention, and more specifically, the cured product containing the curable composition of the present invention is a flexible substrate.
- This is an overcoat film for a flexible wiring board provided on part or all of the surface of the flexible wiring board on which the wiring is formed.
- the flexible wiring board of the present invention is a flexible wiring board in which a part or all of the surface on which the wiring is formed of the flexible wiring board formed by wiring on the flexible substrate is covered with the overcoat film. is there.
- the wiring covered with the overcoat film is preferably a tin-plated copper wiring in view of the oxidation prevention and economical aspect of the wiring.
- the manufacturing method of the flexible wiring board of this invention is a manufacturing method of the flexible wiring board coat
- Step 1 ′ Step of forming a printed film on the pattern by printing the curable composition of the present invention on at least a part of the wiring pattern portion of the flexible wiring board (Step 2 ′) Obtained in Step 1 ′
- the curable composition of the present invention can be used, for example, as an ink for an overcoat film for insulation protection of wiring, and the cured product of the present invention can be used as an overcoat film for insulation protection.
- the cured product of the present invention can be used as an overcoat film for insulation protection.
- a flexible wiring board such as a chip-on-film (COF)
- COF chip-on-film
- the overcoat film of the flexible wiring board can be formed through the following step 1 and step 3 and step 2 as necessary.
- Process 1 The process of forming a printed film on this pattern by printing the curable composition of this invention in at least one part of the wiring pattern part of a flexible wiring board (process 2) A step of evaporating a part or all of the solvent in the printed film by placing the printed film obtained in step 1 in an atmosphere of 40 to 100 ° C. (step 3) A step of curing the printed film obtained in step 1 or the printed film obtained in step 2 at 100 to 170 ° C. to form an overcoat film.
- the temperature at which the solvent in the printed film is evaporated by placing the printed film obtained in Step 1 in an atmosphere of 40 to 100 ° C., which is carried out in Step 2, depends on the evaporation rate of the solvent and the subsequent operation (100 to 100 ° C.). In consideration of a rapid transition to an operation of curing by heating at 170 ° C., the temperature is usually 40 to 100 ° C., preferably 60 to 100 ° C., and more preferably 70 to 90 ° C.
- the time for evaporating the solvent in the printed film by placing the printed film obtained in Step 1 in the atmosphere of 40 to 100 ° C. carried out in Step 2 is not particularly limited, but preferably 10 to 120. Minutes, more preferably 20 to 100 minutes.
- thermosetting evaporating the solvent in the printed film by placing the printed film obtained in Step 1 in an atmosphere of 40 to 100 ° C.
- the process proceeds to Step 3 and is heated at 100 to 170 ° C. to cure and form an overcoat film, and the curing reaction and the solvent removal may be performed together.
- the conditions for the thermosetting performed here are preferably 105 to 160 ° C., more preferably 110 from the viewpoint of preventing diffusion of the plating layer and obtaining low warpage and flexibility suitable as a protective film.
- ⁇ 150 ° C There is no particular limitation on the heat curing time for curing by heating to form an overcoat film, but it is preferably 10 to 150 minutes, more preferably 15 to 120 minutes.
- a flexible wiring board in which wiring is formed on a flexible substrate a flexible wiring board in which a part or all of the surface on which the wiring is formed is covered with the overcoat film can be obtained. it can.
- the curable composition of the present invention is blended with the above-described optional components as necessary, and is uniformly mixed, and as a film forming material, an overcoat ink for semiconductor elements and various electronic components, solder resist ink, interlayer insulation Besides being useful as a film, it can also be used as a paint, a coating agent, an adhesive and the like.
- A represents the acid value (mgKOH / g)
- Vf represents the titration amount (mL) of the 0.1N KOH solution
- Wp represents the mass (g) of the solution containing (Component A).
- I represents the ratio (mass%) of the component (A) of the solution containing (component A).
- the hydroxyl value was 35.4 mg-KOH / g.
- the terminal acid anhydride group-containing imide prepolymer having a solid content concentration of 30% by mass was heated to 100 ° C. and stirred to obtain 950.8 parts by mass of polyester diol ( ⁇ ) and 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene (manufactured by Osaka Gas Chemicals, trade name: BPEF) 82.7 parts by mass and ⁇ -butyrolactone 1200.5 parts by mass were added and stirred.
- BPEF 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene
- BPEF 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene
- BPEF 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene
- BPEF 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene
- compound (A-1) a solution of a compound having an imide bond and a hydroxyl group (hereinafter referred to as “compound (A-1)”) having a solid content concentration of 40% by mass was obtained.
- the number average molecular weight of the compound (A-1) was 15000, the degree of dispersion was 4.0, the acid value of the solid content was 25 mgKOH / g, and the aromatic ring concentration calculated from the preparation ratio was 5.0 mmol / g.
- the terminal acid anhydride group-containing imide prepolymer having a solid content concentration of 30% by mass was heated to 100 ° C. and stirred, and a polyester polyol of 3-methyl-1,5-pentanediol: isophthalic acid (manufactured by Kuraray Co., Ltd.).
- Product name 950.8 parts by mass of Kuraray polyol P-3030 (*) and 9,9-bis [4- (2-hydroxyethoxy) phenyl] fluorene (product name: BPEF, 82.7, made by Osaka Gas Chemical) Part by mass and 1200.5 parts by mass of ⁇ -butyrolactone were added and stirred.
- TDI Cosmonate T-80 (Mitsui Chemical Polyurethane Co., Ltd.)
- DBU 1,8-diazabicyclo [5.4.0] -7-undecene
- the terminal acid anhydride group-containing imide prepolymer having a solid content concentration of 30% by mass was heated to 100 ° C. and stirred to obtain 950.8 parts by mass of polyester diol ( ⁇ ) and 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene (trade name: BPEF, manufactured by Osaka Gas Chemicals) 82.7 parts by mass and ⁇ -butyrolactone 1239.4 parts by mass were added and stirred.
- BPEF 9,9-bis [4- (2-Hydroxyethoxy) phenyl] fluorene
- compound (A-3) a solution of a compound having an imide bond and a hydroxyl group (hereinafter referred to as “compound (A-3)”) having a solid content concentration of 40% by mass was obtained.
- the number average molecular weight of the compound (A-3) was 15000, the degree of dispersion was 4.0, the acid value of the solid content was 26 mgKOH / g, and the aromatic ring concentration was 4.8 mmol / g.
- TDI Cosmonate T-80 (Mitsui Chemical Polyurethane Co., Ltd.)
- DBU 1,8-diazabicyclo [5.4.0] -7-undecene
- the terminal acid anhydride group-containing imide prepolymer having a solid content concentration of 30% by mass was heated to 100 ° C. and stirred, and a polyester polyol of 3-methyl-1,5-pentanediol: isophthalic acid (manufactured by Kuraray Co., Ltd.).
- compound (A-4) 4-dimethylaminopyridine (DMAP) was added as a catalyst and reacted at 100 ° C. for 8 hours. Thereafter, by cooling to room temperature, a solution of a compound having an imide bond and a hydroxyl group (hereinafter referred to as “compound (A-4)”) having a solid content concentration of 40% by mass was obtained.
- the number average molecular weight of the compound (A-4) was 15000, the degree of dispersion was 4.0, the acid value of the solid content was 26 mgKOH / g, and the aromatic ring concentration was 4.8 mmol / g.
- reaction solution was raised to 180 ° C. and reacted at 180 ° C. for 2 hours. Subsequently, the temperature of the reaction solution was lowered to 120 ° C., 5.61 g of 2-butanone oxime (manufactured by Wako Pure Chemical Industries, Ltd.) was added, the reaction was terminated, and the mixture was cooled to room temperature, whereby an amide having a solid content concentration of 40 mass% was obtained.
- a solution of a compound having a bond, an imide bond and a carboxyl group hereinafter referred to as “compound (A-5)”) was obtained.
- the number average molecular weight of the obtained compound (A-5) was 10,500, the degree of dispersion was 3.1, the acid value of the solid content was 24 mgKOH / g, and the aromatic ring concentration was 4.7 mmol / g.
- reaction solution was raised to 180 ° C. and reacted at 180 ° C. for 2 hours. Subsequently, the temperature of the reaction solution was lowered to 120 ° C., 5.61 g of 2-butanone oxime (manufactured by Wako Pure Chemical Industries, Ltd.) was added, the reaction was terminated, and the mixture was cooled to room temperature, whereby an amide having a solid content concentration of 40% by mass was obtained.
- a solution of a compound having a bond, an imide bond and a carboxyl group hereinafter referred to as “compound (A-6)”) was obtained.
- the number average molecular weight of the obtained compound (A-6) was 10,500, the degree of dispersion was 3.1, the acid value of the solid content was 24 mgKOH / g, and the aromatic ring concentration was 4.7 mmol / g.
- the temperature of the reaction solution is lowered to 80 ° C., 16.40 g (0.158 mol) of neopentyl glycol (manufactured by Kanto Chemical Co., Ltd.) as a diol is added, and the temperature is raised to 120 ° C. to dissolve all raw materials, and 4 hours Reacted. Thereafter, the temperature of the reaction solution is lowered to 80 ° C., and 9.67 g (0.105 mol) of glycerin (manufactured by Kanto Chemical Co., Ltd.) as a triol and 39.10 g of ⁇ -butyrolactone (manufactured by Mitsubishi Chemical Co., Ltd.) are added. The temperature was raised to 0 ° C.
- the reaction was carried out while confirming the presence of the isocyanate group in the reaction solution by IR measurement.
- the reaction is terminated, and the reaction mixture is cooled to room temperature.
- a solution of a compound having an amide bond, an imide bond and a hydroxyl group (hereinafter referred to as “compound (A-7)”) was obtained.
- the compound (A-7) obtained has a number average molecular weight of 10,000, a dispersity of 4.3, an acid value of solid content of 15 mgKOH / g, a hydroxyl value of 10 mgKOH / g, and an aromatic ring concentration of 3.3 mmol / g. Met.
- the terminal acid anhydride group-containing imide prepolymer having a solid content concentration of 30% by mass was heated to 100 ° C. and stirred, and derived from 3-methyl-1,5-pentanediol: 1,6-hexanediol.
- Polycarbonate polyol containing a structural unit Keraray Co., Ltd., trade name: Kuraray polyol C-3090 (*)) 950.8 parts by mass and 9,9-bis [4- (2-hydroxyethoxy) phenyl] fluorene (Osaka) 82.7 parts by mass of Gas Chemical, trade name: BPEF) and 1200.5 parts by mass of ⁇ -butyrolactone were added and stirred.
- reaction solution was raised to 180 ° C. and reacted at 180 ° C. for 2 hours. Subsequently, the temperature of the reaction solution was lowered to 120 ° C., 5.61 g of 2-butanone oxime (manufactured by Wako Pure Chemical Industries, Ltd.) was added, the reaction was terminated, and the mixture was cooled to room temperature, whereby an amide having a solid content concentration of 40 mass% was obtained.
- a solution of a compound having a bond, an imide bond and a carboxyl group hereinafter referred to as “compound (A-9)”) was obtained.
- the number average molecular weight of the obtained compound (A-9) was 10,500, the degree of dispersion was 3.1, the acid value of the solid content was 24 mgKOH / g, and the aromatic ring concentration was 1.8 mmol / g.
- a polycarbonate diol compound trade name: DURANOL T5650E: manufactured by Asahi Kasei Chemicals Corporation
- Mn 500
- compound (C ⁇ -1) a compound having an imide bond, a carboxyl group and a hydroxyl group having a solid content concentration of 40 mass%.
- the number average molecular weight of the compound (CA-1) was 10,500, the degree of dispersion was 4.0, the acid value of the solid content was 44 mgKOH / g, and the aromatic ring concentration was 0.7 mmol / g.
- reaction solution was raised to 180 ° C. and reacted at 180 ° C. for 2 hours. Subsequently, the temperature of the reaction solution was lowered to 120 ° C., 3.13 g of 2-butanone oxime (manufactured by Wako Pure Chemical Industries, Ltd.) was added, the reaction was terminated, and the mixture was cooled to room temperature, whereby an amide having a solid content concentration of 40 mass% was obtained.
- a solution of a compound having a bond, an imide bond and a carboxyl group hereinafter referred to as “compound (CA-2) was obtained.
- the compound (CA-2) obtained had a number average molecular weight of 12,200, a degree of dispersion of 3.1, an acid value of solid content of 14 mgKOH / g, and an aromatic ring concentration of 0.6 mmol / g.
- a reaction vessel equipped with a stirrer, a thermometer, and a condenser contains a structural unit derived from 1,4-cyclohexanedimethanol and a structural unit derived from 1,6-hexasandiol in a molar ratio of 3: 1.
- the temperature of the reaction solution is lowered to 80 ° C., 16.40 g (0.158 mol) of neopentyl glycol (manufactured by Kanto Chemical Co., Ltd.) as a diol is added, and the temperature is raised to 120 ° C. to dissolve all raw materials, and 4 hours Reacted. Thereafter, the temperature of the reaction solution is lowered to 80 ° C., and 9.67 g (0.105 mol) of glycerin (manufactured by Kanto Chemical Co., Ltd.) as a triol and 26.07 g of ⁇ -butyrolactone (manufactured by Mitsubishi Chemical Co., Ltd.) are added. The temperature was raised to 0 ° C.
- reaction was allowed to proceed.
- the reaction is carried out while confirming the presence of the isocyanato group in the reaction solution by IR measurement.
- the reaction is terminated, and 177.1 g of ⁇ -butyrolactone is added to obtain a solid concentration of 40
- the compound (CA-3) obtained has a number average molecular weight of 8000, a degree of dispersion of 4.4, an acid value of solid content of 27 mgKOH / g, a hydroxyl value of 16 mgKOH / g, and an aromatic ring concentration of 0.5 mmol / g. Met.
- composition example 2 of curing agent solution ⁇ B-2 solution>
- an epoxy resin mainly composed of N, N-diglycidyl-4- (glycidyloxy) aniline manufactured by Mitsubishi Chemical Corporation, grade name: JER630, epoxy equivalent 98 g / eqv) ) 16.85 parts by mass and 18.25 parts by mass of diethylene glycol diethyl ether were added and stirring was started.
- curable composition F1 a curable composition
- Examples 2 to 10 of the curable composition and Comparative Examples 1 to 3 The curable composition was blended according to the blending composition shown in Table 1 by the same method as in Example 1.
- the formulations prepared in Examples 2 to 9 were referred to as main agent formulations F2 to F10, respectively, and the formulations prepared in Comparative Examples 1 to 3 of the curable composition were referred to as comparative main agent formulations G1 to G3, respectively.
- a block isocyanate “7950” manufactured by Baxenden corresponding to (Component B) was further blended.
- surface represents a "mass part.”
- Table 2 shows the composition of the curable compositions F1 to F10 and the curable compositions G1 to G3.
- Table 3 shows a summary of the parts by mass of the components of the curable compositions F1 to F10 and the curable compositions G1 to G3.
- the number of epoxy groups / the number of carboxyl groups in Tables 2 and 3 was calculated from the acid value.
- a flexible copper-clad laminate manufactured by Sumitomo Metal Mining Co., Ltd., grade name: Esperflex, copper thickness: 8 ⁇ m, polyimide thickness: 38 ⁇ m
- the curable composition F1 was applied by screen printing so as to have a thickness of 15 ⁇ m, held at room temperature for 10 minutes, and cured by placing it in a 120 ° C. hot air circulating dryer for 60 minutes.
- the protective PET film on the backing of the prepared test piece was peeled off, cut into a strip shape with a width of 10 mm with a cutter knife, bent about 180 degrees so that the coating surface was on the outside, and 0.5 ⁇ using a compressor. Compressed at 0.2 MPa for 3 seconds. The bent part was bent and observed with a 30-fold microscope to confirm the presence or absence of cracks.
- Table 4 The same evaluation was performed using the curable compositions F2 to F10 and the curable compositions G1 to G3. The results are also shown in Table 4.
- the curable composition F1 was applied to a substrate by screen printing with a # 180 mesh polyester plate, and the substrate was placed in a hot air circulation dryer at 80 ° C. for 30 minutes. Then, the applied curable composition F1 was cured by placing the substrate in a 120 ° C. hot air circulation dryer for 60 minutes. As the substrate, a 25 ⁇ m-thick polyimide film [Kapton (registered trademark) 100EN, manufactured by Toray DuPont Co., Ltd.] was used.
- the cured coating film was cut to a diameter of 50 mm ⁇ with a circle cutter together with the substrate. What is cut into a circle exhibits a deformation in which the vicinity of the center warps in a convex or concave shape.
- the one that has been cut with a circle cutter and has a cured film formed on the substrate is placed in a convex state after 1 hour, that is, with the cured film formed on the substrate so that the vicinity of the center is in contact with the horizontal plane.
- the maximum and minimum values of the warp height from the horizontal plane were measured, and the average value was obtained.
- the sign indicates the direction of warping.
- the curable composition of the present invention is excellent in flexibility, wire breakage suppression and long-term electrical insulation reliability, and the cured product is useful as an insulating protective film for flexible wiring boards.
- the curable composition of the present invention can be suitably used for insulation protection of flexible wiring boards.
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Abstract
Description
(成分B)硬化剤、および
(成分C)有機溶媒
を含有することを特徴とする硬化性組成物。
[3](成分A)が、芳香環濃度が1.0~6.0mmol/gである[1]または[2]に記載の硬化性組成物。
[4](成分A)が、(原料a)酸無水物基を有する3価及び/又は4価のポリカルボン酸誘導体、(原料b)下記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール、(原料c)ポリイソシアネート、および(原料d)下記式(A2)及び/又は(A3)を原料に用いて反応させて得られる化合物を含有することを特徴とする[1]~[3]のいずれかに記載の硬化性組成物。
即ち、[4]で規定される重合組成物は、その構造または特性をもって特定することが不可能であり、プロセス(製法)によって初めて特定することが可能となり、「出願時において当該物をその構造または特性により直接特定することが不可能またはおよそ非実際的である事情が存在すると考える。
[4'](成分A)が、(原料a)酸無水物基を有する3価及び/又は4価のポリカルボン酸誘導体、(原料b)下記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール、(原料c)ポリイソシアネート、および(原料d)下記式(A2)及び/又は(A3)を原料からなる反応生成物を含有することを特徴とする[1]に記載の硬化性組成物。
[6](成分A)の酸価が10~50mgKOH/gであることを特徴とする[1]~[5]のいずれかに記載の硬化性組成物。
[7](成分B)が、1分子あたり2個以上のエポキシ基を有する化合物を含むことを特徴とする[1]~[6]のいずれかに記載の硬化性組成物。
[8](成分C)が、エーテル系溶媒、エステル系溶媒、ケトン系溶媒、及び芳香族炭化水素系溶媒からなる群から選ばれる少なくとも1種の有機溶媒であることを特徴とする[1]~[7]のいずれかに記載の硬化性組成物。
[9]さらに、(成分D)無機微粒子および有機微粒子からなる群から選ばれる少なくとも1種の微粒子を含むことを特徴とする[1]~[8]のいずれかに記載の硬化性組成物。
[10]成分(A)と成分(B)の合計量を100質量部としたとき、成分(B)を1~55質量部含むことを特徴とする[1]~[9]のいずれかに記載の硬化性組成物。
[11]成分(A)、成分(B)、成分(C)、および成分(D)の合計量(成分(D)を含まない場合は、成分(A)、成分(B)、および成分(C)の合計量)を100質量部としたとき、成分(C)を25~75質量部含むことを特徴とする[1]~[10]のいずれかに記載の硬化性組成物。
[13]前記[1]~[11]のいずれかに記載の硬化性組成物をフレキシブル基板上に配線が形成されてなるフレキシブル配線板の、配線が形成されている表面の一部又は全部に塗布し硬化することによって得られるフレキシブル配線板用オーバーコート膜。
[14]フレキシブル基板上に配線が形成されてなるフレキシブル配線板の、配線が形成されている表面の一部又は全部が、前記[13]に記載のオーバーコート膜によって被覆されてなることを特徴とするフレキシブル配線板。
[15]配線が、錫メッキ銅配線であることを特徴とする[14]に記載のフレキシブル配線板。
[16]下記(工程1)および(工程3)と必要に応じて(工程2)とを含むことを特徴とする、オーバーコート膜によって被覆されたフレキシブル配線板の製造方法;
(工程1)
前記[1]~[11]のいずれか1に記載の硬化性組成物を、フレキシブル配線板の配線パターン部の少なくとも一部に印刷することで該パターン上に印刷膜を形成する工程
(工程2)
工程1で得られた印刷膜を40~100℃の雰囲気下におくことで印刷膜中の溶媒の一部または全量を蒸発させる工程
(工程3)
工程1で得られた印刷膜または工程2で得られた印刷膜を、100~170℃で加熱することによって、硬化させ、オーバーコート膜を形成する工程。
[17]前記[12]に記載の硬化膜を有する電子部品。
なお、本明細書に記載の「(n+1)個のR1は、それぞれ独立に」という表現は、(n+1)個のR1は、すべて同じ構造であっても、一部が同じ構造であり、他の一部が異なる構造であっても、すべてが異なる構造であっても、いっこうに構わないことを意味する。また、本明細書に記載の「n個のR2は、それぞれ独立に」および「(m+1)個のR3は、それぞれ独立に」という表現も同様に、n個のR2および(m+1)個のR3、すべて同じ構造であっても、一部が同じ構造であり、他の一部が異なる構造であっても、すべてが異なる構造であっても、いっこうに構わないことを意味する。
硬化性組成物
本発明は、
(成分A)下記式(A)で表される構造単位を少なくとも1つ有し、かつイミド結合およびアミド結合の少なくとも1方の結合を有し、かつ硬化剤と反応する官能基を有する化合物、
(成分B)硬化剤、および
(成分C)有機溶媒
を含有することを特徴とする硬化性組成物である。
本発明の硬化性組成物の必須成分である(成分A)は、式(A)で表される構造単位を有し、かつイミド結合
(方法1)
(原料b)下記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール
(原料c)ポリイソシアネートと(原料a)酸無水物基を有する3価および/または4価のポリカルボン酸誘導体とを反応させて、イミド結合およびアミド結合の少なくとも1方の結合を有し、末端にイソシアナト基を有するポリイソシアネートを得、これに、(原料b)前記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール及び、(原料d)前記式(A2)及び/又は(A3)で表されるジオール化合物とを反応させる。
(原料c)ポリイソシアネートと(原料a)酸無水物基を有する3価および/または4価のポリカルボン酸誘導体とを反応させて、イミド結合およびアミド結合の少なくとも1方の結合を有しかつ末端に酸無水物基および/またはカルボキシル基を有する化合物を得、これに、(原料b)前記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール及び(原料d)前記式(A2)及び/又は(A3)で表されるジオールを反応させる。
方法1の合成法では、まず、(原料b)前記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール及び、(原料d) 前記式(A2)及び/又は式(A3)のジオール化合物を、(原料c)ポリイソシアネートと反応させて、ウレタン結合を有しかつ末端にイソシアナト基を有するポリイソシアネート化合物(以下「(A1-1)化合物」と記す。)を合成する。
式(1)中、(n+1)個のR1は、それぞれ独立に3~36個の炭素を有するジオールから誘導される有機残基である。いいかえると、上記ジオールから誘導される有機残基とは、ジオールからヒドロキシ基が2個とれた2価の基である。
1,2-シクロペンタンジメタノール、1,3-シクロペンタンジメタノール及びビス(ヒドロキシメチル)トリシクロ[5.2.1.0]デカン等の5員環ジオール、並びに、1,2-シクロヘキサンジオール、1,3-シクロヘキサンジオール、1,4-シクロヘキサンジオール、1,2-シクロヘキサンジメタノール、1,3-シクロヘキサンジメタノール、1,4-シクロヘキサンジメタノール、及び2,2-ビス(4-ヒドロキシシクロヘキシル)-プロパン等の6員環ジオール等の脂環構造を有するジオール等を挙げることができる。R1はこれらのジオールから末端水酸基が外れた構造である。
1,2-シクロペンタンジメタノール、1,3-シクロペンタンジメタノール及びビス(ヒドロキシメチル)トリシクロ[5.2.1.0]デカン等の5員環ジオール、並びに、1,2-シクロヘキサンジオール、1,3-シクロヘキサンジオール、1,4-シクロヘキサンジオール、1,2-シクロヘキサンジメタノール、1,3-シクロヘキサンジメタノール、1,4-シクロヘキサンジメタノール、及び2,2-ビス(4-ヒドロキシシクロヘキシル)-プロパン等の6員環ジオール等の脂環構造を有するジオール等を挙げることができる。
(原料c)として、(原料b)および(原料d)と反応させるポリイソシアネートが使用される。(原料c)ポリイソシアネートとしては、イソシアナト基を2つ以上有する化合物であれば、特に制限はない。ポリイソシアネートの具体例としては、1,3-シクロヘキサンジイソシアネート、1,4-シクロヘキサンジイソシアネート、イソホロンジイソシアネート、4,4'-ジシクロヘキシルメタンジイソシアネート、1,3-ビス(イソシアナトメチル)シクロヘキサン、1,4-ビス(イソシアナトメチル)シクロヘキサン、ノルボルネンジイソシアネートおよびイソホロンジイソシアネートのビウレット体等の環状脂肪族ポリイソシアネート;
ジフェニルメタン-2,4′-ジイソシアネート、3,2′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、3,3′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、4,2′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、4,3′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、5,2′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、5,3′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、6,2′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、6,3′-ジメチルジフェニルメタン-2,4′-ジイソシアネート、3,2′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、3,3′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、4,2′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、4,3′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、5,2′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、5,3′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、6,2′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、6,3′-ジエチルジフェニルメタン-2,4′-ジイソシアネート、3,2′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、3,3′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、4,2′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、4,3′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、5,2′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、5,3′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、6,2′-ジメトキシジフェニルメタン-2,4′-ジイ
ソシアネート、6,3′-ジメトキシジフェニルメタン-2,4′-ジイソシアネート、4,4'-ジフェニルメタンジイソシアネート、ジフェニルメタン-3,3′-ジイソシアネート、ジフェニルメタン-3,4′-ジイソシアネート、ジフェニルエーテル-4,4′-ジイソシアネート、ベンゾフェノン-4,4′-ジイソシアネート、ジフェニルスルホン-4,4′-ジイソシアネート、2,4-トリレンジイソシアネート、2,6-トリレンジイソシアネート、m-キシリレンジイソシアネート、p-キシリレンジイソシアネート、1,5-ナフタレンジイソシアネート、4,4′-[2,2ビス(4-フェノキシフェニル)プロパン]ジイソシアネート等の芳香環を有するポリイソシアネート;
ヘキサメチレンジイソシアネートのビウレット体、リシントリイソシアネート、リシンジイソシアネート、ヘキサメチレンジイソシアネート、2,4,4-トリメチルヘキサメチレンジイソシアネートおよび2,2,4-トリメチルヘキサンメチレンジイソシアネート鎖状脂肪族ポリイソシアネート;イソホロンジイソシアネートのイソシアヌレート体、ヘキサメチレンジイソシアネートのイソシアヌレート体等の複素環を有するポリイソシアネート等を挙げることができ、これらを単独で用いても、2種以上を組み合わせて用いてもよい。
酸無水物基を有する3価のポリカルボン酸誘導体としては、コスト面等から、無水トリメリット酸が特に好ましい。
酸無水物基を有する4価のポリカルボン酸誘導体についても特に限定されないが、例えば、下記一般式(5)で表されるテトラカルボン酸二無水物を挙げることができる。これらは、1種を単独で又は2種以上を組み合わせて使用することができる。
末端にイソシアナト基を有する(A'-1)化合物と、(原料a)との混合比率は、最終的に生成する化合物が、ウレタン結合と、アミド結合および/またはイミド結合を有する範囲であれば特に制限されない。
(方法2)の合成法では、先ず、(原料c)ポリイソシアネートと(原料a)酸無水物基を有する3価および/または4価のポリカルボン酸誘導体酸とを反応させて、イミド結合およびアミド結合の少なくとも1方の結合を有するポリイソシアネート(以下、「(A2-1)」化合物と記す。)を合成する。これに、(原料b)前記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール及び(原料d)前記式(A2)及び/又は(A3)で表されるジオール化合物を、反応させる。
(方法3)の合成法では、先ず、(原料c)ポリイソシアネートと(原料a)酸無水物基を有する3価および/または4価のポリカルボン酸誘導体酸とを反応させて、イミド結合およびアミド結合の少なくとも1方の結合を有しかつ末端に酸無水物基および/またはカルボキシル基を有する化合物(以下、「(A3-1)化合物」と記す。)を合成する。
上記非含窒素系極性溶媒は、例えば、ジエチレングリコールジメチルエーテル、ジエチレングリコールジエチルエーテル、トリエチレングリコールジメチルエーテル及びトリエチレングリコールジエチルエーテル等のエーテル系溶媒;ジメチルスルホキシド、ジエチルスルホキシド、ジメチルスルホン及びスルホラン等の含硫黄系溶媒;γ-ブチロラクトン及び酢酸セロソルブ等のエステル系溶媒;シクロヘキサノン及びメチルエチルケトン等のケトン系溶媒;並びに、トルエン及びキシレン等の芳香族炭化水素系溶媒から選ばれる。これらは1種類を単独で又は2種類以上組み合わせて使用することができる。
(a)数平均分子量(Mn)
Mn=Σ(NiMi)/ΣNi=ΣXiMi
(Xi=分子量Miの分子のモル分率=Ni/ΣNi)
(b)質量平均分子量(Mw)
Mw=Σ(NiMi 2)/ΣNiMi=ΣWiMi
(Wi=分子量Miの分子の質量分率=NiMi/ΣNiMi)
(c)分子量分布(分散度)
分散度=Mw/Mn
ある。
装置名:日本分光株式会社製HPLCユニット HSS-2000
カラム:Shodex(登録商標)カラムLF-804×3本(直列)
移動相:テトラヒドロフラン
流速:1.0mL/min
検出器:日本分光株式会社製RI-2031Plus
温度:40.0℃
試料量:サンプルループ 100μリットル
試料濃度:0.1質量%前後に調整。
A=10×Vf×56.1/(Wp×I)・・・・・式(α)
により酸価を算出する。式(α)中、Aは酸価(mgKOH/g)を示し、Vfは0.1NのKOH溶液の滴定量(mL)を示し、Wpは(成分A)を含む溶液の質量(g)を示し、Iは(成分A)を含む溶液の不揮発分の割合(質量%)を示す。
本実施形態に係る硬化性組成物は、前記(成分A)を硬化させることのできる硬化剤を更に含有する。硬化剤としては、成分(A)の官能基と反応しうる官能基を1分子中に2個以上有する化合物である。成分(A)が、カルボキシル基、水酸基、酸無水物基、イソシアナト基、アミド基、アミノ基のいずれかを有するとき、成分(B)の硬化剤はそれらの官能基と反応するエポキシ基、イソシアナト基、水酸基、カルボキシル基を複数個有することが好ましい。
後述の本発明の硬化膜の長期電気絶縁性能を重視する場合には、1分子中に2個以上のエポキシ基を有しかつ芳香環構造および/または脂環構造を有する化合物の中で、ジシクロペンタジエン変性フェノール樹脂のグリシジルエーテル(即ち、トリシクロ[5,2,1,02,6]デカン構造および芳香環構造を有しかつ2個以上のエポキシ基を有する化合物)、1,3-ビス(1-アダマンチル)-4,6-ビス(グリシジロイル)ベンゼン、1-[2′,4′-ビス(グリシジロイル)フェニル]アダマンタン、1,3-ビス(4′-グリシジロイルフェニル)アダマンタンおよび1,3-ビス[2′,4′-ビス(グリシジロイル)フェニル]アダマンタン等のアダマンタン構造を有するエポキシ樹脂(即ち、トリシクロ[3,3,1,13,7]デカン構造および芳香環構造を有しかつ2個以上のエポキシ基を有する化合物)等のトリシクロデカン構造および芳香環構造を有しかつ2個以上のエポキシ基を有する化合物が吸水率の低い硬化物を提供できるので好ましく、特に好ましくは、下記式(6)に記載の化合物である。
成分Cとして用いられる有機溶媒としては、(成分A)、および(成分B)を溶解できる溶剤であれば、特に制限はないが、例えば、ジエチレングリコールジメチルエーテル、ジエチレングリコールジエチルエーテル、ジエチレングリコールエチルメチルエーテル、ジエチレングリコールジブチルエーテル、ジエチレングリコールブチルメチルエーテル、ジエチレングリコールイソプロピルメチルエーテル、トリエチレングリコールジメチルエーテル、トリエチレングリコールブチルメチルエーテル、テトラエチレングリコールジメチルエーテル、ジプロピレングリコ-ルジメチルエーテル、トリプロピレングリコールジメチルエーテル等のエーテル系溶媒、エチレングリコールモノメチルエーテルアセテート、エチレングリコールモノエチルエーテルアセテート、プロピレングリコールモノメチルエーテルアセテート、プロピレングリコールモノエチルエーテルアセテート、ジプロピレングリコールモノメチルエーテルアセテート、ジプロピレングリコールモノエチルエーテルアセテート、ジエチレングリコールモノエチルエーテルアセテート、ジエチレングリコールモノメチルエーテルアセテート、メトキシプロピオン酸メチル、メトキシプロピオン酸エチル、エトキシプロピオン酸メチル、エトキシプロピオン酸エチル、γ-ブチロラクトン等のエステル系溶媒、デカヒドロナフタリン等の炭化水素系溶媒、シクロヘキサノン等のケトン系溶媒、トルエン、キシレン等の芳香族炭化水素系溶媒を挙げることができ、これらの溶媒を単独で用いても、2種類以上を併用しても良い。
また、本発明の硬化性組成物は、(成分D)として無機微粒子および有機微粒子からなる群から選ばれる少なくとも1種の微粒子を含むことが好ましい。
本発明の硬化性組成物に使用されるシリカ微粒子は、粉末状で物理的に被覆或いは有機化合物で化学的に表面処理されたな微粒子も含むものと定義する。
これらのアエロジルに代表されるシリカ微粒子は、スクリーン印刷時の印刷性を付与するために使用されることもあり、その場合にはチクソ性の付与を目的として使用される。
これらの無機微粒子および/または有機微粒子の平均粒子径は、好ましくは0.01~10μm、さらに好ましくは0.1~5μmである。
本発明の硬化性組成物において、(成分D)を分散させる方法としては、通常、塗料分野で行われているロール練り、ミキサー混合等が適用され、十分な分散が行われる方法であればよい。
さらに、本発明の硬化性組成物は、印刷の際の泡の発生を消す或いは抑制する目的で、消泡剤を含むことができ、かつ含むことが好ましい。
さらに、本発明の硬化性組成物は、硬化促進剤を含むことができ、かつ含むことが好ましい。硬化促進剤としては、エポキシ基とカルボキシル基の反応を促進する化合物であれば特に限定されるものではなく、例えば、メラミン、アセトグアナミン、ベンゾグアナミン、2,4-ジアミノ-6-メタクリロイルオキシエチル-S-トリアジン、2,4-メタクリロイルオキシエチル-s-トリアジン、2,4-ジアミノ-6-ビニル-s-トリアジン、2,4-ジアミノー6-ビニル-s-トリアジン・イソシアヌル酸付加物等のトリアジン系化合物、イミダゾール、2-メチルイミダゾール、2-エチル-4-メチルイミダゾール、2-フェニルイミダゾール、2-ウンデシルイミダゾール、2-ヘプタデシルイミダゾール、1-ベンジルー2-メチルイミダゾール、2-フェニルー4-メチルイミダゾール、1-シアノエチル-2-メチルイミダゾール、1-シアノエチル-2-エチル-4-メチルイミダゾール、1-アミノエチルー2-エチルー4-メチルイミダゾール、1-アミノエチル-2-メチルイミダゾール、1-(シアノエチルアミノエチル)-2-メチルイミダゾール、N-[2-(2-メチルー1-イミダゾリル)エチル]尿素、1-シアノエチル-2-ウンデシルイミダゾール、1-シアノエチル-2-メチルイミダゾリウムトリメリテート、1-シアノエチル-2-フェニルイミダゾリウムトリメリテート、1-シアノエチル-2-エチル-4-メチルイミダゾリウムトリメリテート、1-シアノエチル-2-ウンデシルイミダゾリウムトリメリテート、2,4-ジアミノ-6-[2′-メチルイミダゾリル-(1′)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2′-ウンデシルイミダゾリル-(1′)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2′-エチル-4′-メチルイミダゾリル-(1′)]-エチル-s-トリアジン、1-ドデシル-2-メチル-3-ベンジルイミダゾリウムクロライド、N,N′-ビス(2-メチル-1-イミダゾリルエチル)尿素、N,N′-ビス(2-メチル-1-イミダゾリルエチル)アジポアミド、2-フェニル-4-メチル-5-ヒドロキシメチルイミダゾール、2-フェニル-4.5-ジヒドロキシメチルイミダゾール、2-メチルイミダゾール・イソシアヌル酸付加物、2-フェニルイミダゾール・イソシアヌル酸付加物、2,4-ジアミノ-6-[2′-メチルイミダゾリル-(1′)]-エチル-s-トリアジン・イソシアヌル酸付加物、2-メチルー4-フォルミルイミダゾール、2-エチルー4-メチルー5-フォルミルイミダゾール、2-フェニル-4-メチルフォルミルイミダゾール、1-ベンジル-2-フェニルイミダゾール、1,2-ジメチルイミダゾール、1-(2-ヒドロキシエチル)イミダゾール、ビニルイミダゾール、1-メチルイミダゾール、1-アリルイミダゾール、2-エチルイミダゾール、2-ブチルイミダゾール、2-ブチル-5-ヒドロキシメチルイミダゾール、2,3-ジヒドロ-1H-ピロロ[1,2-a]ベンズイミダゾール、1-ベンジル-2-フェニルイミダゾール臭化水素塩、1-ドデシル-2-メチル-3-ベンジルイミダゾリウムクロライド等のイミダゾール化合物、1,5-ジアザビシクロ(4.3.0)ノネン-5およびその塩、1,8-ジアザビシクロ(5.4.0)ウンデセン-7およびその塩等のジアザビシクロアルケンなどのシクロアミジン化合物およびシクロアミジン化合物の誘導体、トリエチレンジアミン、ベンジルジメチルアミン、トリエタノールアミン、ジメチルアミノエタノール、トリス(ジメチルアミノメチル)フェノール等のアミン系化合物、トリフェニルホスフィン、ジフェニル(p-トリル)ホスフィン、トリス(アルキルフェニル)ホスフィン、トリス(アルコキシフェニル)ホスフィン、トリス(アルキル・アルコキシフェニル)ホスフィン、トリス(ジアルキルフェニル)ホスフィン、トリス(トリアルキルフェニル)ホスフィン、トリス(テトラアルキルフェニル)ホスフィン、トリス(ジアルコキシフェニル)ホスフィン、トリス(トリアルコキシフェニル)ホスフィン、トリス(テトラアルコキシフェニル)ホスフィン、トリアルキルホスフィン、ジアルキルアリールホスフィン、アルキルジアリールホスフィン等のホスフィン系化合物、ジシアンジアジド等を挙げることができる。
これらの硬化促進剤の中で、硬化促進作用および電気絶縁性能を両立させることを考慮すると、好ましいものとしては、メラミン、イミダゾール化合物、シクロアミジン化合物、シクロアミジン化合物の誘導体、ホスフィン系化合物およびアミン系化合物であり、さらに好ましくは、メラミン、1,5-ジアザビシクロ(4.3.0)ノネン-5およびその塩、1,8-ジアザビシクロ(5.4.0)ウンデセン-7およびその塩である。
本発明の硬化膜は、本発明の硬化性組成物を硬化することで得ることができる硬化物を含む。また本発明の電子部品は上記硬化膜を有する。
さらに、本発明のフレキシブル配線板の製造方法は、下記の工程1'および工程2'を含む、オーバーコート膜によって被覆されたフレキシブル配線板の製造方法である。
(工程2')工程1'で得られた印刷膜、工程1'で得られた印刷膜を40~100℃の雰囲気下におくことで印刷膜中の溶媒の一部を蒸発させた一部の溶媒が除去された印刷膜、または工程1'で得られた印刷膜を40~100℃の雰囲気下におくことで印刷膜中の溶媒の全量を蒸発させた全量の溶媒が除去された印刷膜を、100~170℃で加熱することによって硬化させ、オーバーコート膜を形成する工程。
(工程1)
本発明の硬化性組成物を、フレキシブル配線板の配線パターン部の少なくとも一部に印刷することで該パターン上に印刷膜を形成する工程
(工程2)
工程1で得られた印刷膜を40~100℃の雰囲気下におくことで印刷膜中の溶媒の一部または全量を蒸発させる工程
(工程3)
工程1で得られた印刷膜または工程2で得られた印刷膜を、100~170℃で加熱することによって、硬化させ、オーバーコート膜を形成する工程。
<酸価の測定>
本発明に使用する(成分A)を含む溶液を以下の方法によって酸価を測定し、式(α)を用いて、(成分A)の酸価を求めた。ただし、前記溶液に用いた溶媒には、酸価が「0」のものを用いる。
A=10×Vf×56.1/(Wp×I)・・・・・式(α)
により酸価を算出する。式(α)中、Aは酸価(mgKOH/g)を示し、Vfは0.1NのKOH溶液の滴定量(mL)を示し、Wpは(成分A)を含む溶液の質量(g)を示し、Iは(成分A)を含む溶液の成分(A)の割合(質量%)を示す。
JIS K0070に準拠して水酸基価を測定した。
<数平均分子量の測定>
数平均分子量はGPCで測定したポリスチレン換算の数平均分子量であり、GPCの測定条件は以下のとおりである。
装置名:日本分光株式会社製HPLCユニット HSS-2000
カラム:Shodex(登録商標)カラムLF-804×3本(直列)
移動相:テトラヒドロフラン
流速:1.0mL/min
検出器:日本分光株式会社製RI-2031Plus
温度:40.0℃
試料量:サンプルループ 100μリットル
試料濃度:0.1質量%前後に調整。
硬化性組成物のチクソトロピー指数を以下の方法により測定した。
硬化性組成物約0.8gを使用して、コーン/プレート型粘度計(Brookfield社製 型式;DV-II+Pro スピンドルの型番;CPE-52)を用いて、温度25.0℃、回転数10rpmの条件で測定開始から7分経過後の粘度を測定した。その後、温度25.0℃、回転数1rpmの条件で測定開始から7分経過後の粘度を測定した。
なお、チクソトロピー指数は以下の計算により求めた。
チクソトロピー指数の求め方:
チクソトロピー指数=[1rpmの粘度]÷[10rpmの粘度]
(参考合成例1) <ポリエステルジオール(α)>
攪拌装置、温度計および蒸留装置付きコンデンサーを備えた反応容器に、無水フタル酸1684.6g(11.56mol)、1,6-ヘキサンジオール1484.5g(12.55mol)を添加して、オイルバスを用いて反応容器の内温を140℃に昇温して、4時間撹拌を継続した。その後、撹拌を継続しながら、モノ-n-ブチル錫オキサイド2.96gを添加して、徐々に反応容器の内温を昇温して、真空ポンプを接続して、少しずつ反応容器内の圧力を減圧していき、水を反応容器外に減圧蒸留により除去していった。最終的には、内温を220℃まで昇温し、圧力を133.32Paまで減圧した。15時間経過して水が完全に留去しなくなったのを確認して反応を終了した。得られたポリエステルポリオール(以下、ポリエステルジオール(α)と記す。)は、前述の式(1)の構造を持ち、n=1~20であった。その水酸基価を測定したところ、水酸基価は35.4mg-KOH/gであった。
(合成例1) <А-1溶液>
攪拌機、冷却管、窒素導入管及び温度計を装備した四つ口フラスコに、テトラカルボン酸二無水物として、3,3′,4,4′-ベンゾフェノンテトラカルボン酸二無水物(BTDA)270.7質量部と、溶剤としてγ-ブチロラクトン964.4質量部を加え、120℃にて撹拌、溶解した。そこへ、ジイソシアネート化合物として4,4'-ジフェニルメタンジイソシアネート(MDI)142.6質量部を添加・撹拌し、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、窒素気流下、120℃で3時間反応させた。その後、室温まで冷却することで固形分濃度30質量%の末端酸無水物基含有イミドプレポリマーを得た。
攪拌機、冷却管、窒素導入管及び温度計を装備した四つ口フラスコに、テトラカルボン酸二無水物として、3,3′,4,4′-ベンゾフェノンテトラカルボン酸二無水物(BTDA)270.7質量部と、溶剤としてγ-ブチロラクトン964.4質量部を加え、120℃にて撹拌、溶解した。そこへ、ジイソシアネート化合物として4,4'-ジフェニルメタンジイソシアネート(MDI)142.6質量部を添加・撹拌し、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、窒素気流下、120℃で3時間反応させた。その後、室温まで冷却することで固形分濃度30質量%の末端酸無水物基含有イミドプレポリマーを得た。
(※ 前述の式(1)の構造をもつポリエステルポリオールで、nの平均は12.0~12.1)
攪拌機、冷却管、窒素導入管及び温度計を装備した四つ口フラスコに、テトラカルボン酸二無水物として、3,3′,4,4′-ベンゾフェノンテトラカルボン酸二無水物(BTDA)270.7質量部と、溶剤としてγ-ブチロラクトン863.2質量部を加え、120℃にて撹拌、溶解した。そこへ、ジイソシアネート化合物として2,4-トリレンジイソシアネートと2,6-トリレンジイソシアネートとの質量比80:20の混合物であるコスモネートT-80(三井化学ポリウレタン株式会社製)(TDI)99.3質量部を添加・撹拌し、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、窒素気流下、120℃で3時間反応させた。その後、室温まで冷却することで固形分濃度30質量%の末端酸無水物基含有イミドプレポリマーを得た。
攪拌機、冷却管、窒素導入管及び温度計を装備した四つ口フラスコに、テトラカルボン酸二無水物として、3,3′,4,4′-ベンゾフェノンテトラカルボン酸二無水物(BTDA)270.7質量部と、溶剤としてγ-ブチロラクトン863.2質量部を加え、120℃にて撹拌、溶解した。そこへ、ジイソシアネート化合物として2,4-トリレンジイソシアネートと2,6-トリレンジイソシアネートとの質量比80:20の混合物であるコスモネートT-80(三井化学ポリウレタン株式会社製)(TDI)99.3質量部を添加・撹拌し、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、窒素気流下、120℃で3時間反応させた。その後、室温まで冷却することで固形分濃度30質量%の末端酸無水物基含有イミドプレポリマーを得た。
攪拌装置、温度計、コンデンサーを備えた反応容器にポリエステルジオール(α)を567.4g(0.1mol)と9,9-ビス[4-(2-ヒドロキシエトキシ)フェニル]フルオレン(大阪ガスケミカル製、商品名:BPEF)34.65g(0.08mol)を入れ、4,4'-ジフェニルメタンジイソシアネートであるMILLIONATE MT(日本ポリウレタン工業株式会社製)53.65g(0.214mol)、及び、2,4-トリレンジイソシアネートと2,6-トリレンジイソシアネートとの質量比80:20の混合物であるコスモネートT-80(三井化学ポリウレタン株式会社製)24.89g(0.143mol)と、γ-ブチロラクトン1021gとを仕込み、150℃ですべての原料を溶解させ、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、4時間反応させて、ウレタン結合を有するポリイソシアネートを生成させた。
得られた化合物(A-5)の数平均分子量は10500、分散度は3.1、固形分の酸価は24mgKOH/gであった、芳香環濃度は、4.7mmol/gであった。
攪拌装置、温度計、コンデンサーを備えた反応容器に3-メチル-1,5-ペンタンジオール:イソフタル酸のポリエステルポリオール(クラレ社製 商品名:クラレポリオールP-3030)567.4g(0.1mol)と9,9-ビス[4-(2-ヒドロキシエトキシ)フェニル]フルオレン(大阪ガスケミカル製、商品名:BPEF)34.65g(0.08mol)を入れ、4,4'-ジフェニルメタンジイソシアネートであるMILLIONATE MT(日本ポリウレタン工業株式会社製)53.65g(0.214mol)、及び、2,4-トリレンジイソシアネートと2,6-トリレンジイソシアネートとの質量比80:20の混合物であるコスモネートT-80(三井化学ポリウレタン株式会社製)24.89g(0.143mol)と、γ-ブチロラクトン1021gとを仕込み、150℃ですべての原料を溶解させ、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、4時間反応させて、ウレタン結合を有するポリイソシアネートを生成させた。
得られた化合物(A-6)の数平均分子量は10500、分散度は3.1、固形分の酸価は24mgKOH/g、芳香環濃度は、4.7mmol/gであった。
攪拌装置、温度計、コンデンサーを備えた反応容器に、ポリエステルジオール(α)369.85g(0.117mol)と9,9-ビス[4-(2-ヒドロキシエトキシ)フェニル]フルオレン(大阪ガスケミカル製、商品名:BPEF)25.58g(0.058mok)、4,4'-ジシクロヘキシルメタンジイソシアネートであるデスモジュール-W(住化バイエルウレタン株式会社製)91.70g(0.350mol)と、溶媒であるγ-ブチロラクトン(三菱化学株式会社製)730.6gとを仕込み、150℃ですべての原料を溶解させ、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、4時間反応させて、ウレタン結合を有するポリイソシアネートを生成させた。
攪拌機、冷却管、窒素導入管及び温度計を装備した四つ口フラスコに、テトラカルボン酸二無水物として、3,3′,4,4′-ベンゾフェノンテトラカルボン酸二無水物(BTDA)270.7質量部と、溶剤としてγ-ブチロラクトン964.4質量部を加え、120℃にて撹拌、溶解した。そこへ、ジイソシアネート化合物として4,4'-ジフェニルメタンジイソシアネート(MDI)142.6質量部を添加・撹拌し、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、窒素気流下、120℃で3時間反応させた。その後、室温まで冷却することで固形分濃度30質量%の末端酸無水物基含有イミドプレポリマーを得た。
(※ 前述の式(1)の構造をもつポリエステルポリオールで、nの平均は12.0~12.1)
攪拌装置、温度計、コンデンサーを備えた反応容器に3-メチル-1,5-ペンタンジオール:1,6-ヘキサンジオールのポリカーボネートポリオール(クラレ社製 商品名:クラレポリオールC-3090)567.4g(0.1mol)と9,9-ビス[4-(2-ヒドロキシエトキシ)フェニル]フルオレン(大阪ガスケミカル製、商品名:BPEF)34.65g(0.08mol)を入れ、4,4'-ジフェニルメタンジイソシアネートであるMILLIONATE MT(日本ポリウレタン工業株式会社製)53.65g(0.214mol)、及び、2,4-トリレンジイソシアネートと2,6-トリレンジイソシアネートとの質量比80:20の混合物であるコスモネートT-80(三井化学ポリウレタン株式会社製)24.89g(0.143mol)と、γ-ブチロラクトン1021gとを仕込み、150℃ですべての原料を溶解させ、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、4時間反応させて、ウレタン結合を有するポリイソシアネートを生成させた。
得られた化合物(A-9)の数平均分子量は10500、分散度は3.1、固形分の酸価は24mgKOH/g、芳香環濃度は、1.8mmol/gであった。
攪拌機、冷却管、窒素導入管及び温度計を装備した四つ口フラスコに、テトラカルボン酸二無水物として、1,2,3,4-ブタンテトラカルボン酸無水物(製品名:リカシッドBT-100、新日本理化製)166.4質量部と、溶剤としてγ-ブチロラクトン398.4質量部を加え、120℃にて撹拌、溶解した。そこへ、ジイソシアネート化合物として2,4-トリレンジイソシアネートと2,6-トリレンジイソシアネートとの質量比80:20の混合物であるコスモネートT-80(三井化学ポリウレタン株式会社製)99.18質量部を添加・撹拌し、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、窒素気流下、120℃で3時間反応させた。その後、室温まで冷却することで固形分濃度40質量%の末端酸無水物基含有イミドプレポリマーを得た。
攪拌装置、温度計、コンデンサーを備えた反応容器に、3-メチル-1,5-ペンタンジオール:1、6-ヘキサンジオールのポリカーボネートポリオール(クラレ社製 商品名:クラレポリオールC-3090)567.4g(0.179mol)を入れ、4,4'-ジシクロヘキシルメタンジイソシアネートであるデスモジュール-W(住化バイエルウレタン株式会社製)56.07g(0.214mol)、及び、1,3-ビス(イソシアナトメチル)シクロヘキサン(商品名:タケネート600、三井化学ポリウレタン株式会社製)27.77g(0.143mol)と、γ-ブチロラクトン976.9gとを仕込み、150℃ですべての原料を溶解させ、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、4時間反応させて、ウレタン結合を有するポリイソシアネートを生成させた。
得られた化合物(CA-2)の数平均分子量は12200、分散度は3.1、固形分の酸価は14mgKOH/g、芳香環濃度は、0.6mmol/gであった。
攪拌装置、温度計、コンデンサーを備えた反応容器に、1,4-シクロヘキサンジメタノールに由来する構成単位と1,6-ヘキササンジオールに由来する構成単位とを3:1のモル比で含んでいるポリカーボネートジオール(UM―CARB90(3/1)、宇部興産株式会社製、平均分子量:約900)156.98g(0.175mol)と、4,4'-ジシクロヘキシルメタンジイソシアネートであるデスモジュール-W(住化バイエルウレタン株式会社製)91.70g(0.350mol)と、溶媒であるγ-ブチロラクトン(三菱化学株式会社製)165.80gとを仕込み、150℃ですべての原料を溶解させ、ここに触媒として1,8-ジアザビシクロ[5.4.0]-7-ウンデセン(DBU)0.1質量部を添加し、4時間反応させて、ウレタン結合を有するポリイソシアネートを生成させた。
(主剤配合物1)
化合物(A-1)を160.0質量部、シリカ粉(日本アエロジル株式会社製,商品名:アエロジルR-974)6.3質量部、硬化促進剤としてメラミン(日産化学工業株式会社製)0.72質量部およびジエチレングリコールジエチルエーテル8.4質量部を混合し、三本ロールミル(株式会社井上製作所製,型式:S-4 3/4×11)を用いて、化合物(A-1)へのシリカ粉、硬化促進剤の混合を行った。その後、消泡剤(モメンティブ・パフォーマンス・マテリアルズ社製,商品名:TSA750S)2.0質量部を添加して、スパチュラを用いて混合した。この配合物を主剤配合物C1とした。
主剤配合物1と同様の方法によって、表1に示す配合組成に従って配合した。それぞれ主剤配合物2~9、比較主剤配合物比1~比3とした。
尚、表中の数値は「質量部」を表す。
(硬化剤溶液の配合例1) <B-1溶液>
撹拌機、温度計およびコンデンサーを備えた容器に、下記式(7)の構造を有するエポキシ樹脂(三菱化学社製,グレード名:JER604,エポキシ当量120g/eqv)16.85質量部、ジエチレングリコールジエチルエーテル18.25質量部を添加し、撹拌を開始した。
撹拌機、温度計およびコンデンサーを備えた容器に、N,N- ジグリシジル-4-(グリシジルオキシ)アニリンを主成分とするエポキシ樹脂(三菱化学株式会社製,グレード名:JER630,エポキシ当量98g/eqv)16.85質量部、ジエチレングリコールジエチルエーテル18.25質量部を添加し、撹拌を開始した。
(硬化性組成物の実施例1)
主剤配合物C1を88.71質量部と硬化剤溶液B-1を3.51質量部とをプラスチック容器に入れた。さらに、後述する他の配合例、比較配合例の硬化性組成物と粘度を合わせるために、溶媒としてジエチレングリコールジエチルエーテル3.0質量部およびジエチレングリコールエチルエーテルアセテート1.5質量部を添加した。混合は、スパーテルを用い、室温で5分間攪拌することで行い、硬化性組成物(以下、「硬化性組成物F1」と記す。)を得た。
硬化性組成物の実施例1と同様の方法によって、表1に示す配合組成に従って配合した。実施例2~9で調製した配合物を、それぞれ主剤配合物F2~F10、硬化性組成物の比較例1~3で調製した配合物を、それぞれ比較主剤配合物G1~G3とした。ここで、硬化性組成物F8、G3においては、さらに(成分B)に相当するBaxenden社製ブロックイソシアネート「7950」も配合した。尚、表中の数値は「質量部」を表す。
硬化性組成物F1~F10、硬化性組成物G1~G3を用いて、以下に説明する方法により、可撓性、断線抑制性、反り性の評価および長期電気絶縁信頼性の評価を行った。その結果を表4に記す。
フレキシブル銅張り積層板(住友金属鉱山株式会社製,グレード名:エスパーフレックス,銅厚:8μm、ポリイミド厚:38μm)の銅上に、幅75mm、長さ110mmの大きさ、硬化後の塗膜の厚み15μmになるように硬化性組成物F1を、スクリーン印刷により塗布し、10分間室温で保持し、120℃の熱風循環式乾燥機に60分間入れることにより硬化させた。作製した試験片の裏打ちの保護PETフィルムを剥離し、幅10mmの短冊状にカッターナイフで切り出した後、塗膜面が外側になる様に約180度折り曲げ、圧縮機を用いて0.5±0.2MPaで3秒間圧縮した。屈曲部を曲げた状態で30倍の顕微鏡で観察し、クラックの発生の有無を確認した。結果を表4に記す。
また、硬化性組成物F2~F10、硬化性組成物G1~G3を用いて、同様の評価を行った。それらの結果もあわせて表4に記す。
フレキシブル銅張り積層板(住友金属鉱山株式会社製,グレード名:エスパーフレックスUS,銅厚:8μm、ポリイミド厚:38μm)をエッチングして製造した、JPCA-ET01に記載の微細くし形パターン形状の基板(銅配線幅/銅配線間幅=15μm/15μm)に錫メッキ処理を施したフレキシブル配線板に、硬化性組成物F1を、スクリーン印刷法により、塗膜のポリイミド面からの厚みが10μmの厚さ(乾燥後)になるように塗布した。得られた塗膜形成配線板を、80℃の熱風循環式乾燥機に30分間入れ、その後、120℃の熱風循環式乾燥機に120分間入れることにより前記塗膜を硬化させた。
この試験片を用いて、JIS C-5016に記載のやり方で下記の試験条件で実施した。
試験機:テスター産業株式会社製 MITテスターBE202
折り曲げ速度:10回/分
荷重:200g
折り曲げ角度:±90°
つかみ具先端部の半径:0.5mm
上記試験条件で10回ずつ折り曲げ回数を増やしていき、目視にて配線のクラックの有無を観察し、クラックが発生したときの折り曲げ回数を記録した。結果を表4に記す。
また、硬化性組成物F2~F10、硬化性組成物G1~G3を用いて、同様の評価を行った。それらの結果についてもあわせて表4に記す。
硬化性組成物F1を、#180メッシュポリエステル版で、基板にスクリーン印刷により塗布し、該基板を80℃の熱風循環式乾燥機に30分間入れた。その後、前記基板を120℃の熱風循環式乾燥機に60分間入れることにより、塗布した硬化性組成物F1を硬化させた。前記基板としては、25μm厚ポリイミドフィルム〔カプトン(登録商標)100EN、東レ・デュポン株式会社製〕を用いた。
また、硬化性組成物F2~F10、硬化性組成物G1~G3を用いて、同様の評価を行った。それらの結果もあわせて表4に記す。
フレキシブル銅張り積層板(住友金属鉱山株式会社製,グレード名:エスパーフレックスUS,銅厚:8μm,ポリイミド厚:38μm)をエッチングして製造した、JPCA-ET01に記載の微細くし形パターン形状の基板(銅配線幅/銅配線間幅=15μm/15μm)に錫メッキ処理を施したフレキシブル配線板に、硬化性組成物F1を、スクリーン印刷法により、ポリイミド面からの厚みが15μmの厚さ(乾燥後)になるように塗布した。前記フレキシブル配線板を80℃の熱風循環式乾燥機に30分間入れ、その後、120℃の熱風循環式乾燥機に120分間入れることにより、塗布した硬化性組成物F1を硬化させた。
Claims (17)
- 前記硬化剤と反応する官能基が、カルボキシル基、水酸基、酸無水物基、イソシアナト基、アミド基、アミノ基の少なくとも1種であることを特徴とする請求項1に記載の硬化性組成物。
- (成分A)が、芳香環濃度が1.0~6.0mmol/gである請求項1または2に記載の硬化性組成物。
- (成分A)が、(原料a)酸無水物基を有する3価及び/又は4価のポリカルボン酸誘導体、(原料b)下記一般式(1)、一般式(2)の少なくとも1方で表されるポリオール、(原料c)ポリイソシアネート、および(原料d)下記式(A2)及び/又は(A3)を原料に用いて反応させて得られる化合物を含有することを特徴とする請求項1~3のいずれか1項に記載の硬化性組成物。
- (成分A)が、前記式(A)で示される構造単位を有し、かつイミド結合およびアミド結合の少なくとも1方の結合を有し、さらにウレタン結合を有する化合物であることを特徴とする請求項1~4のいずれか1項に記載の硬化性組成物。
- (成分A)の酸価が10~50mgKOH/gであることを特徴とする請求項1~5のいずれか1項に記載の硬化性組成物。
- (成分B)が、1分子あたり2個以上のエポキシ基を有する化合物を含むことを特徴とする請求項1~6のいずれか1項に記載の硬化性組成物。
- (成分C)が、エーテル系溶媒、エステル系溶媒、ケトン系溶媒、及び芳香族炭化水素系溶媒からなる群から選ばれる少なくとも1種の有機溶媒であることを特徴とする請求項1~7のいずれか1項に記載の硬化性組成物。
- さらに、(成分D)無機微粒子および有機微粒子からなる群から選ばれる少なくとも1種の微粒子を含むことを特徴とする請求項1~8のいずれか1項に記載の硬化性組成物。
- 成分(A)と成分(B)の合計量を100質量部としたとき、成分(B)を1~55質量部含むことを特徴とする請求項1~9のいずれか1項に記載の硬化性組成物。
- 成分(A)、成分(B)、成分(C)、および成分(D)の合計量(成分(D)を含まない場合は、成分(A)、成分(B)、および成分(C)の合計量)を100質量部としたとき、成分(C)を25~75質量部含むことを特徴とする請求項1~10のいずれか1項に記載の硬化性組成物。
- 請求項1~11のいずれか1項に記載の硬化性組成物の硬化物を含む硬化膜。
- 請求項1~11のいずれか1項に記載の硬化性組成物をフレキシブル基板上に配線が形成されてなるフレキシブル配線板の、配線が形成されている表面の一部又は全部に塗布し硬化することによって得られるフレキシブル配線板用オーバーコート膜。
- フレキシブル基板上に配線が形成されてなるフレキシブル配線板の、配線が形成されている表面の一部又は全部が、請求項13に記載のオーバーコート膜によって被覆されていることを特徴とするフレキシブル配線板。
- 配線が、錫メッキ銅配線であることを特徴とする請求項14に記載のフレキシブル配線板。
- 下記(工程1)および(工程3)と必要に応じて(工程2)とを含むことを特徴とする、オーバーコート膜によって被覆されたフレキシブル配線板の製造方法;
(工程1)
請求項1~11のいずれか1項に記載の硬化性組成物を、フレキシブル配線板の配線パターン部の少なくとも一部に印刷することで該パターン上に印刷膜を形成する工程
(工程2)
工程1で得られた印刷膜を40~100℃の雰囲気下におくことで印刷膜中の溶媒の一部または全量を蒸発させる工程
(工程3)
工程1で得られた印刷膜または工程2で得られた印刷膜を、100~170℃で加熱することによって、硬化させ、オーバーコート膜を形成する工程。 - 請求項12に記載の硬化膜を有する電子部品。
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JP2019147887A (ja) * | 2018-02-27 | 2019-09-05 | Jnc株式会社 | 熱硬化性組成物 |
WO2020090634A1 (ja) * | 2018-10-31 | 2020-05-07 | 三井化学株式会社 | ベンダブル配線基板、伸縮できる配線基板およびそれらによる電子デバイス |
JPWO2020090634A1 (ja) * | 2018-10-31 | 2021-05-13 | 三井化学株式会社 | ベンダブル配線基板、伸縮できる配線基板およびそれらによる電子デバイス |
US11542377B2 (en) | 2018-10-31 | 2023-01-03 | Mitsui Chemicals, Inc. | Bendable circuit board, expandable circuit board, and electronic device made therefrom |
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WO2023182432A1 (ja) * | 2022-03-23 | 2023-09-28 | 帝人株式会社 | 熱硬化性プリプレグ及びその製造方法 |
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CN109071954B (zh) | 2021-11-02 |
TWI653251B (zh) | 2019-03-11 |
CN109071954A (zh) | 2018-12-21 |
TW201809050A (zh) | 2018-03-16 |
KR20180126029A (ko) | 2018-11-26 |
KR102112437B1 (ko) | 2020-05-18 |
JPWO2017183497A1 (ja) | 2019-02-21 |
JP6882264B2 (ja) | 2021-06-02 |
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