JP2818768B2 - Crosslinkable curable resin composition - Google Patents

Description

Description: TECHNICAL FIELD The present invention relates to a photopolymerizable or radiation polymerizable resin composition that can be developed with an aqueous alkaline solution.

[Conventional technology]

In recent years, a so-called dry film resist having a structure in which a photopolymerizable resin layer is sandwiched between a support film and a protective film as a photoresist for producing a printed wiring board has been widely used. As the photopolymerizable resin layer, there are known a solvent development type in which an unexposed portion is developed and removed with a chlorine-based organic solvent and an alkali development type in which an unexposed portion is developed and removed with an aqueous alkali solution. Alkaline development type dry film resists are becoming mainstream because of the influence and the advantage of manufacturing cost.

The method of using an alkali development type dry film resist having a protective film and a support film is as follows. First, while peeling the protective film from the dry film resist, the photopolymerizable resin surface is heat-laminated on a copper-clad laminate, and then the resist is formed. A photo tool is brought into close contact with the supporting film surface of the film, and the hardened portions are exposed and cured by ultraviolet rays or the like. Next, after the support film is peeled off, the unexposed portions are developed and removed with a weak alkaline aqueous solution such as sodium carbonate to obtain a resist circuit pattern. Thereafter, in the case of the copper through-hole method, after etching the copper surface, the cured resist is peeled off with a strong alkali aqueous solution such as sodium hydroxide to obtain a printed wiring board. In the case of the solder through-hole method, after performing copper plating and solder plating, the hardened resist is peeled off with a strong alkaline aqueous solution, and the exposed copper is etched to obtain a printed wiring board.

During the above process, it is natural that the dry film resist must have sufficient resistance as an etching resist or a plating resist. Until now, various kinds of resists have been mainly used to improve such resistance. Considerations have been made.

However, many conventional alkali-developed dry film resists have the disadvantage that the time required for peeling off the cured resist with a strong alkaline aqueous solution (stripping time) is long. If the stripping time is long, the copper surface of the substrate is oxidized and discolored by alkali, which adversely affects processes such as etching, and in the case of the solder through hole method, the solder is dissolved by a strong alkaline aqueous solution. Therefore, during the etching step, the pattern may be thinned or broken, or the fusing may not be performed.

On the other hand, conventional alkaline-developed dry film resists having a short stripping time have the disadvantage that cured resist strips separated by a strongly alkaline stripping plate are easily dissolved in the stripping solution. Was. When the cured resist strip is easily dissolved in the stripping solution, the strip is easily swollen and gelled while the strip remains in the stripping tank, and the gel-like material is passed through a stripping machine to collect the strip. Frequent clogging of the provided filters. As a result, the circulation amount of the stripping liquid decreases and the hardened resist cannot be stripped,
In some cases, the stripping solution overflowed from the stripping tank and contaminate the periphery of the tank.

Further, among the conventional alkali-developed dry film resists having a short stripping time, the size of the cured resist strip which has been stripped by a strong alkali stripping solution is too large. Or it had the disadvantage of being too small. If the peeled piece was too large (> 45 mm square), the peeled piece could cling to the transport roller of the automatic peeling machine, causing trouble in the device. For this reason, Japanese Patent Application Laid-Open No. Sho 64-10235 discloses an attempt to reduce the size of a peeled piece by using a specific crosslinkable monomer, but when the peeled piece is fine (<2 mm square). ) 、 Since it is easy to pass through the mesh of the filter for collecting strips provided in the stripping machine, the strips enter into the liquid circulation pump or spray nozzle and hinder circulation of stripping solution or strip without being removed Due to the strips staying in the solution for a long time, the stripping solution deteriorates rapidly or the strips dissolve and the liquid must be replaced frequently.

As described above, in the conventional dry film resist, it was not possible to simultaneously satisfy a short stripping time, an appropriate size of a stripping piece, and insolubility of the stripping piece in a stripping solution.

[Problems to be solved by the invention]

An object of the present invention is to overcome the above-mentioned drawbacks, to shorten the stripping time, to make the strips of an appropriate size, and to easily dissolve the strips in the stripping solution. It is to provide a resin composition.

[Means for solving the problem]

The present inventors have conducted intensive studies to achieve the above object, and as a result, have found that these objects can be achieved by using the following photopolymerizable resin composition, leading to drying of the present invention. .

That is, the present invention provides: (a) 15 to 35% by weight of a first polymerizable substance comprising one or more compounds of an α, β-unsaturated carboxyl group-containing monomer having 3 to 15 carbon atoms; General formula [I] Wherein R ₁ is H, an alkyl group having 1 to 6 carbon atoms or a halogen atom, and one or more compounds selected from the group consisting of ring-substituted derivatives thereof. (2) 2 to 25% by weight of a polymerizable substance, one selected from the group consisting of an alkyl acrylate having an alkyl group having 1 to 8 carbon atoms and a hydroxyalkyl acrylate having a hydroxyalkyl group having 2 to 8 carbon atoms or 10 to 40% by weight of a third polymerizable substance comprising a further compound, wherein the alkyl group comprises alkyl methacrylate having 1 to 8 carbon atoms and the hydroxyalkyl group comprises hydroxyalkyl methacrylate having 2 to 8 carbon atoms. A fourth polymerizable material consisting of one or more compounds selected from the group, copolymerized with 30 to 65% by weight 40 to 70 parts by weight of a thermoplastic polymer for a binder, (b) a general formula [II] (Wherein R ₂ is an alkylene group having 3 to 6 carbon atoms,
R ₃ and R ₄ are H or CH ₃ , and n is a positive integer such as 5 to 9) wherein at least one ethylenic compound is contained in one molecule containing 51 to 100% by weight of a compound represented by the formula: Crosslinkable monomer 25 having an unsaturated group
To 50 parts by weight and (c) 0 to 10 parts by weight of the photopolymerization initiator in a total amount of 100
It is a cross-linking curable resin composition that is combined so as to be parts by weight.

The thermoplastic polymer for a binder constituting the crosslinkable resin composition of the present invention contains an α, β-unsaturated carboxyl group having 3 to 15 carbon atoms so that it can be developed with a dilute aqueous alkali solution such as sodium carbonate. It is necessary to copolymerize one or more of the contained monomers as the first polymerizable substance at a ratio of 15 to 35% by weight. Examples of this carboxylic acid type monomer that can be used include acrylic acid, methacrylic acid, cinnamic acid, crotonic acid, sorbic acid, itaconic acid,
There are propiolic acid, maleic acid and fumaric acid, and half esters or anhydrides thereof can also be used. The most preferred of these are acrylic acid and methacrylic acid. These carboxylic acid type components have a content in the copolymer of 15 to 35% by weight, preferably 18 to 35% by weight.
It is desirable to use it so as to be in the range of about 30% by weight.
When the content of the carboxylic acid component in the copolymer is less than 15% by weight, development cannot be carried out with an aqueous alkali solution or the development time is too long, resulting in a decrease in resolution.
On the other hand, when the carboxylic acid copolymerization amount exceeds 35% by weight, the development time becomes too short, the development control becomes difficult to obtain a high-resolution pattern, and the water resistance of the cured portion also decreases. .

The second polymerizable substance to be copolymerized in the binder resin,
General formula [I] (Wherein R ₁ is H, an alkyl group having 1 to 6 carbon atoms or a halogen atom). The benzene ring of the substance may be substituted with a functional group such as a nitro group, an alkoxy group, an acyl group, a carboxyl group, a sulfone group, a hydroxyl group or a halogen. May be used. Preferred substituents are methyl or t.
-A single alkyl group such as a butyl group. The most preferred of these compounds is styrene. These second polymerizable components need to be copolymerized so as to be in the range of 2 to 25% by weight, preferably 3 to 20% by weight in the thermoplastic copolymer for a binder. If the copolymerization amount of the component is less than 2% by weight, it is not possible to obtain a resist material having excellent chemical resistance, in particular, a plating resistance, and if the component exceeds 25% by weight, The resist resin bath of the obtained dry film resist is too hard, so that the resist on the substrate is easily peeled, and the time required for development and peeling becomes long.

The third polymerizable substance that can be contained in the binder resin,
An alkyl acrylate having an alkyl group having 1 to 8 carbon atoms and a hydroxyalkyl acrylate having a hydroxyalkyl group having 2 to 8 carbon atoms. Examples of these compounds include methyl acrylate, ethyl acrylate, n-propyl acrylate, iso-propyl acrylate, n-butyl acrylate, sec-butyl acrylate, t-butyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate And 2-ethylhexyl acrylate. The most preferred of these compounds are
Methyl acrylate, ethyl acrylate, n-butyl acrylate and 2-ethylhexyl acrylate. These acrylate-type components, in order to impart appropriate flexibility to the photopolymerizable or radiation-curable resin composition of the present invention, 10 to 40% by weight of the binder thermoplastic copolymer,
It is necessary to copolymerize so as to be preferably in the range of 15 to 35% by weight. Acrylate type component content of 10
If the amount is less than 10% by weight, a sufficiently flexible dry film resist cannot be obtained, and the adhesion of the resist resin to the substrate and the embedding property of the resist resin into the unevenness of the substrate surface are insufficient, and the resisting resistance of the resist is insufficient. descend. On the other hand, when the copolymerization amount of the third polymerizable substance exceeds 40% by weight, on the other hand, the resist resin is too soft, and when the resist film is wound around a roll and stored, the resist resin becomes less than the support film. Causes a so-called cold flow phenomenon that oozes out with time.

The fourth polymerizable substance copolymerized in the binder resin is copolymerized with the alkyl acrylate or hydroxyalkyl acrylate to give the thermoplastic polymer for a binder an appropriate glass transition temperature (Tg), An alkyl methacrylate having an alkyl group having 1 to 8 carbon atoms and a hydroxyalkyl methacrylate having a hydroxyalkyl group having 2 to 8 carbon atoms. Examples of these compounds include methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, iso-propyl methacrylate, n-butyl methacrylate, sec-butyl methacrylate, t-butyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate And 2-ethylhexyl methacrylate. The most preferred of these compounds is methyl methacrylate. These methacrylate components need to be copolymerized so as to be in the range of 30 to 65% by weight, preferably 35 to 60% by weight in the thermoplastic copolymer for a binder.

In order to achieve the object of the present invention, the thermoplastic polymer for a binder used in the present invention needs to be a polymer composed of the specific monomer, and the weight average molecular weight is in the range of 40,000 to 500,000. Is desirable. Those having a weight average molecular weight of less than 40,000 are liable to cause a cold flow phenomenon when used as a dry film resist, while those having a weight average molecular weight of more than 500,000 have insufficient solubility in an unexposed portion in an alkali developing solution. Developability is poor, and development time is extremely long, which causes a decrease in resolution and a decrease in circuit pattern productivity.

The thermoplastic polymer for the binder used in the present invention, 40 to 70 parts by weight in 100 parts by weight of the photopolymerizable resin composition,
Preferably, the content is 45 to 65 parts by weight. A photopolymerizable resin composition containing less than 40 parts by weight of a thermoplastic polymer for a binder may impair the film forming property of the photosensitive layer of the obtained dry film resist, fail to obtain sufficient film strength, and cause cold flow. Cheap. On the other hand, the content of the thermoplastic polymer is 70
If the amount exceeds the weight part, the photocurable film is fragile, the adhesion to the substrate is impaired, and sufficient chemical resistance, particularly adhesion resistance and etching resistance, cannot be obtained.

In a crosslinkable monomer comprising one or more compounds having one or more ethylenically unsaturated groups in one molecule constituting the composition of the present invention, a compound represented by the general formula [II]: (Wherein R ₂ is an alkylene group having 3 to 6 carbon atoms,
R ₃ and R ₄ are H or CH ₃ , and n is a positive integer such that n = 5 to 9). 55 to 90% by weight. A dry film resist obtained using a crosslinkable monomer having a content of the compound of less than 51% by weight has an increased release time of a cured resist by an aqueous alkali solution, and a release piece is extremely easily dissolved in a release liquid. In addition, it becomes difficult to control the size of the peeled piece to an appropriate size.

In the formula [II], R ₂ is an alkylene group having 3 to 6 carbon atoms. If the R ₂ is obtained by curing the SakuTsuta crosslinkable resin composition using a number 2 following compounds carbon atoms such as polyethylene glycol diacrylate and the like, as well as its crosslinking density is too high stripping time is long, Since the hydrophilicity of the crosslinkable monomer is increased, the strips of the cured resist become too fine and easily dissolved in a stripping solution, which is not preferable. On the other hand, a crosslinkable resin composition prepared by using a compound in which R ₂ has 7 or more carbon atoms is not preferable because, on the contrary, the curability is insufficient and the chemical resistance, particularly the plating resistance and the etching resistance are lowered.

In the formula [II], n is a positive integer such that n = 5 to 9. When a crosslinkable resin composition made using a compound in which n is 4 or less is cured, the crosslink density becomes too high, so that not only the peeling time becomes longer, but also the peeled pieces of the cured resist become too fine and peeled. It is not preferable because it easily passes through the mesh of the filter of the machine. On the other hand, a crosslinkable resin composition prepared using a resin having n of 10 or more has insufficient curability, and not only decreases the chemical resistance, particularly the plating resistance and the etching resistance, but also has a large release piece. It is not preferable because it is too entangled with the transport roller of the peeling machine.

Therefore, in order to obtain a crosslinkable resin composition which simultaneously satisfies good chemical resistance and excellent easy peeling property, insoluble property of stripping pieces and an appropriate size of stripping pieces, the formula (II)
Wherein R ₂ is an alkylene group having 3 to 6 carbon atoms, and n must be in the range of 5 to 9.

As the compound represented by the formula (II), hexa-1,3-
Propanediol di (meth) acrylate (hexa represents n = 6 in the formula [II], 1,3-propanediol represents R ₂ = —CH ₂ CH ₂ CH ₂ —, and (meth) The acrylate indicates that R ₃ , R ₄ ＨH or CH _{3. The} same applies to the following expressions), octa-1,3-propanediol di (meth) acrylate, hexapropylene glycol di (meth) acrylate Octapropylene glycol di (meth) acrylate, nona-1,2-butanediol di (meth) acrylate, hexa-1,3-butanediol di (meth) acrylate, octa-1,3-
Butanediol di (meth) acrylate, penta-1,4
-Butanediol di (meth) acrylate, nona-2,3
-Butanediol di (meth) acrylate, penta-2
-Methyl-1,3-propanediol di (meth) acrylate, hepta-2-methyl-1,3-propanediol di (meth) acrylate, nona-2-methyl-1,3-propanediol di (meth) acrylate , Hepta-1,1-
Dimethyl-1,2-ethanediol di (meth) acrylate, octa-1,2-pentanediol di (meth) acrylate, nona-1,3-pentanediol di (meth) acrylate, hexa-1,4-pentanediol Di (meta)
Acrylate, hepta-1,5-pentanediol di (meth) acrylate, octa-2,3-pentanediol di (meth) acrylate, hepta-2,4-pentanediol di (meth) acrylate, hexa-2,2- Dimethyl-
1,3-propanediol di (meth) acrylate, octa-2,2-dimethyl-1,3-propanediol di (meth)
Acrylate, octa-1,2-hexanediol di (meth) acrylate, hexa-1,3-hexanediol di (meth) acrylate, hepta-1,4-hexanediol di (meth) acrylate, penta-1,5- Hexanediol di (meth) acrylate, hepta-1,6-hexanediol di (meth) acrylate, octa-2,3-hexanediol di (meth) acrylate, nona-2,4-
Hexanediol di (meth) acrylate, hepta-2,
5-hexanediol di (meth) acrylate, hexa-3,4-hexanediol di (meth) acrylate, and the like. Among them, preferred compounds are those represented by the following general formula [III] wherein R ₂ has 3 carbon atoms. Wherein R ₃ and R ₄ are H or CH ₃ and n is n = 5
Pentapropylene glycol di (meth) acrylate, hexapropylene glycol di (meth) acrylate, heptapropylene glycol di (meth) acrylate, octapropylene glycol di (meth) acrylate represented by the following formula: And nonapropylene glycol di (meth) acrylate. Commercial products such as NK-ester 9pG and NK-ester APG-
400 (all manufactured by Shin-Nakamura Chemical Co., Ltd.). A more preferred compound is heptapropyne glycol di (meth) acrylate where n = 7 in the formula [III], and commercially available products such as NK-ester APG-400
(Made by Shin-Nakamura Chemical Co., Ltd.). These may be used alone or in combination of two or more.

The crosslinkable monomer other than the crosslinkable monomer represented by the formula [III] may be any compound having one or more ethylenically unsaturated groups in one molecule. Sidiethoxy (meth) acrylate, polyethylene glycol di (meth) acrylate, 1,3-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, 2, 2-bis [4- (meth) acryloxypolyethoxyphenyl] propane, 2,2-bis [4- (meth) acryloxypolypropyleneoxyphenyl] propane, neopentylglycol di (meth) acrylate hydroxypiparate , Glycerin di (meth) acrylate, glycerin tri (meth) acrylate, trimethylolethanedi ( (T) acrylate, trimethylolethane tri (meth) acrylate, trimethylolpropane di (meth) acrylate, trimethylolpropane tri (meth) acrylate, trimethylolpropane tris [polyethoxy (meth) acrylate], trimethylolpropane tris [polypropyleneoxy (Meth) acrylate], triethylol di (meth) acrylate isocyanurate, triethylol tri (meth) acrylate isocyanurate, pentaerythritol di (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipenta Erythritol tri (meth) acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol (Meth) acrylates of polyhydric alcohols such as ta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, compounds of formula [II] wherein n = 1 to 4, and compounds of formula [II] wherein n is 10 or more; acrylamide derivatives such as n-butoxymethylacrylamide and iso-butoxymethylacrylamide; epoxy (meth) acrylates and urethane (meth) acrylates; and these can be used alone or in combination.
It does not have to be used.

In order to provide the photopolymerizable resin composition of the present invention with excellent easy peelability and an appropriate peeling piece size of the cured resist that is the object of the present invention, and to impart insolubility of the peeling piece to an alkaline solution, It is indispensable to use 25 to 50 parts by weight of a crosslinkable monomer obtained by mixing a specific amount of the crosslinkable monomer represented by the formula [II] with respect to 40 to 70 parts by weight of a specific thermoplastic polymer for a binder. Therefore, a composition outside the scope of the present invention cannot be used as a dry film resist capable of simultaneously achieving excellent easy peelability and an appropriate peeling piece size and peeling piece insolubility which are the objects of the present invention. . The thermoplastic polymer used in the present invention enables the development and stripping of the resist with an aqueous alkali solution by using a specific amount of a carboxylic acid type monomer as a copolymer component as described above. By adding a crosslinkable monomer represented by the formula (1) to these thermoplastic polymers in a specific amount or more, the easily peelable properties, the appropriate size of the peelable pieces, and the properties of the peelable pieces which are unexpectedly excellent from the prior art. Thus, it was possible to obtain a dry film resist capable of exhibiting solubility. Although the detailed mechanism has not been fully elucidated, the use of the crosslinkable monomer represented by the formula [II] allows the photopolymerizable resin composition to be appropriately cured and the crosslinkable monomer to be cured. The non-uniform swelling pressure when the cured resist swells with an alkaline aqueous solution due to the moderate hydrophilicity of the body [II] improves the easy peeling property, and breaks the cured resist into an appropriate size. It is expected that it peeled off. In addition, it is considered that the molecular structure of the crosslinkable monomer [II] is moderately hydrophobic, but the solubility in an aqueous alkaline solution is reduced, and the peeled pieces are insoluble.

The crosslinkable monomer having an ethylenically unsaturated group used in the present invention is contained in an amount of 25 to 50 parts by weight, preferably 30 to 45 parts by weight, per 100 parts by weight of the crosslinkable resin composition of the present invention. When the content of the crosslinkable monomer is less than 25 parts by weight, the photopolymerizable composition is not sufficiently cured by light, and the chemical resistance, particularly the plating resistance and the etching resistance are reduced. On the other hand, when the content of the crosslinkable monomer is more than 50 parts by weight as a dry film resist, cold flow is likely to occur, and the peelability of the photocured product by an aqueous alkali solution is reduced. I do.

The photopolymerization initiator used for photopolymerizing the crosslinkable resin composition of the present invention includes benzophenone, Michler's ketone, 4,4'-bis (diethylamino) benzophenone,
Known materials such as t-butylanthraquinone, 2-ethylanthraquinone, thioxanthones, benzoin alkyl ethers, and benzyl ketals can be used, and one or more of these can be used in combination.

The photopolymerization initiator used in the present invention, when cured with ultraviolet light, 0.1% by weight in 100 parts by weight of the crosslinkable resin composition.
-10 parts by weight. When the amount is less than 0.1 part by weight, the obtained crosslinkable resin composition is not sufficiently cured by light, while when it exceeds 10 parts by weight, it becomes thermally unstable. When the crosslinkable resin composition of the present invention is cured with an electron beam, a photopolymerization initiator may not be contained.

The crosslinkable resin composition of the present invention preferably contains tetrazole or a derivative thereof in order to further improve the plating resistance. Addition of a small amount of tetrazole or a derivative thereof can improve the adhesion to a metal surface, and examples thereof include 1-phenyltetrazole,
-Phenyltetrazole, 5-aminotetrazole, 5
-Amino-1-methyltetrazole, 5-amino-2-
Examples thereof include phenyltetrazole, 5-mercapto-1-phenyltetrazole, 5-mercapto-1-methyltetrazole, and one or more of these can be used in combination. Compounds other than the above-mentioned tetrazoles, such as benzotriazole and benzimidazole, are difficult to obtain excellent effects unless used in large amounts in order to improve the plating resistance, whereas when used in large amounts, the crosslinkable resin composition of the present invention In addition to reducing the sensitivity, these compounds remain on the copper surface even after development or peeling, thereby deteriorating adhesion and delaying etching. The amount of tetrazole or its derivative used is preferably in the range of 0.005 to 5 parts by weight based on 100 parts by weight of the total of the thermoplastic polymer for the binder, the crosslinkable monomer and the photopolymerization initiator. If the amount is less than 0.005 parts by weight, no improvement in the adhesion resistance is clearly observed, while if it exceeds 5 parts by weight, it takes a long time to dissolve in the crosslinkable resin composition, and the sensitivity of the crosslinkable resin composition also increases. descend.

The crosslinkable resin composition of the present invention may contain components such as a thermal polymerization inhibitor, a dye, a plasticizer and a filler, if necessary.

Although the crosslinkable resin composition of the present invention can be formed into a film on a target substrate as it is even in the absence of a diluent, a solvent having a very low boiling point, for example, acetone, methyl ethyl ketone, methyl cellosolve, ethyl cellosolve, It is easier to form a film by dissolving and mixing one or more of dichloromethane, chloroform, methyl alcohol, ethyl alcohol, and isopropyl alcohol. The use amount of these solvents is 200 parts by weight or less, preferably 50 to 150 parts by weight, based on 100 parts by weight of the crosslinkable resin composition.

Further, in order to form a dry film resist using the crosslinkable resin composition of the present invention, a blade coater, a rod coater, a knife coater, a roll doctor coater, a comma coater, a reverse roll coater, a transfer roll coater, a gravure coater, a kiss roll The composition can be applied using a coater, a curtain coater or the like. However, when a solvent is used in the composition, it is necessary to disperse the solvent. As a support, a plastic film such as polyester is mainly used. If a flammable organic solvent is used as the dryer, use a device equipped with an air-heated heat source using steam from the viewpoint of safety.Use a method in which the hot air in the dryer is brought into countercurrent contact and blow it to the support from the nozzle. A method or the like is used. The shape of the dryer is selected and used according to the purpose such as an arch type or a flat type.

If necessary, a protective film such as polyethylene or polypropylene may be laminated on the dried film resist after drying.

The dry film resist manufactured as described above has excellent peelability, peeling piece size and peeling piece insolubility is extremely good, and has excellent workability as an etching and plating resist, process passability, and high resolution pattern. can get.

〔Example〕

 Hereinafter, the present invention will be described specifically with reference to examples.

Synthesis Example 100 g of isopropyl alcohol, 100 g of methyl ethyl ketone and 200 g of a monomer having the composition shown in Table 1 were placed in a 1000 ml four-necked flask equipped with a nitrogen inlet, a stirrer, a condenser, and a thermometer under a nitrogen atmosphere. The temperature of the hot water bath was raised to 80 ° C. while stirring. Next, 1.0 g of azobisisobutyronitrile was dissolved in 10 g of isopropyl alcohol and added, followed by polymerization for 4 hours. Next, 1.0 g of azobisisobutyronitrile was dissolved in 10 g of isopropyl alcohol, and the solution was added in five portions every 30 minutes. The temperature inside the flask was raised to the boiling point of the solvent, and the temperature was increased to 2 hours at that temperature. Polymerized. After completion of the polymerization, 100 g of isopropyl alcohol was added, the polymerization reaction product was taken out of the flask, and a binder resin solution was prepared to obtain binder resin solutions A to F shown in Table 1. The polymerization rate of the monomer mixture in each composition was 99.5% or more. The solid content in the binder resin solution was 38.7% by weight.

Examples 1 to 11 and Comparative Examples 1 to 14 Using the binder resin solutions A to F obtained in the synthesis examples,
A photopolymerizable resin composition having the composition of No. 2 was prepared.

Stir the blended composition with a propeller mixer,
It was applied to a coating width of 340 mm on a polyester film having a thickness of 25 μm and a width of 360 mm by a blade coater. Then width 400
Hot air was blown in countercurrent through a dryer having a thickness of 100 mm, a height of 100 mm, and a length of 8 m to make the dry coating thickness 50 μm. At this time, the coating speed was 5 m / min, and the hot air temperature was 90 ° C. Next, a polyethylene protective film having a thickness of 35 μm was laminated on the dried coating film, and then wound into a roll having a length of 120 m. The roll was left sideways in a constant temperature room at 23 ° C. for 5 days, and the state of cold flow from the roll end face was visually observed. The results are shown in Table 3.

The obtained dry film resist is heat-laminated to the copper clad laminate while the protective film is peeled off,
After the temperature of the copper-clad laminate returned to room temperature, a phototool was adhered to the polyester film surface and exposed with an ultra-high pressure mercury lamp. UHIO USH-102D ultrahigh-pressure mercury lamp, 100mJ
/ cm ² . The exposure intensity at this time was measured by attaching the UVD-365P receiver to Ushio Electric UV intensity meter UIT-100 and measuring 5 times.
mw / cm ² . After being exposed for 20 minutes, the support film was peeled off and developed with a 1% aqueous solution of sodium carbonate. The development was performed with a liquid temperature of 30 ° C., a spray pressure of 1.4 kg / cm ^2, and a distance between the spray and the substrate of 10 cm. Then, after immersion in a neutral degreaser at room temperature for about 1 minute to degrease, spray water washing is performed for about 1 minute in an overflow tank, and then immersed in a 20% ammonium persulfate aqueous solution for 1 minute, and then spray water washing again for about 1 minute Got it. Thereafter, it was immersed in 10% sulfuric acid for 1 minute, and spray-washed again for 1 minute. Next, after immersing in 10% sulfuric acid for 1 minute, immersing in copper sulfate plating solution, 2.3A
Copper plating was performed at / dm ² for 75 minutes. The liquid temperature at this time is 22 ° C
It was. Immediately after the completion of the plating, the plate was washed with water, immersed in a 15% aqueous solution of borofluoric acid for 1 minute, immersed in a high-throw soldering solution, and soldered at 1.8 A / dm ² for 18 minutes.
The liquid temperature at this time was 22 ° C. After the plating, the product was washed with water and then dried. Table 3 shows the plating resistance of each dry film resist. The compositions of the copper plating solution and the solder plating solution are as follows.

(Copper plating liquid) Copper sulfate 75g / 98% sulfuric acid 190g / 36% hydrochloric acid 0.12ml / Luminous agent 5ml / (Soldering liquid) Tin 15g / Lead 10g / Free hydrofluoric acid 400g / Using a sample after free soldering 21.6 g / peptone 5.2 g / solder, the resist was stripped with a 3% sodium hydroxide aqueous solution at 45 ° C. For peeling, the distance between the sample and the spray nozzle was 10 cm, and the spray pressure was 1.
The test was performed at 0 kg / cm ² . At this time, the time required for removing the resist and the size of the strip were measured, and the results are also shown in Table-3.

The peeled pieces after the peeling evaluation were collected, placed in a beaker containing a 3% sodium hydroxide aqueous solution, sealed, and then kept at 45 ° C. for 24 hours using a thermostatic water bath, and visually observed whether the peeled pieces were dissolved. did. The results are also shown in Table 3.

[Effects of the Invention] As described above in detail, by using the crosslinkable resin composition of the present invention for dry film, the peeling time is short,
It is possible to exhibit the characteristic that the peeling piece has an appropriate size, and the peeling piece does not easily dissolve in the peeling solution, and as a result, discoloration of the copper surface due to alkali and peeling of the peeling piece to the solder peeling machine transport roller. The industrial value is extremely large because troubles such as entanglement and rapid deterioration of the stripping solution or clogging of the filter of the stripping machine are eliminated and the production is high.

Continuation of the front page (51) Int.Cl. ⁶ Identification symbol FI G03F 7/027 502 G03F 7/027 502 7/033 7/033 // C08F 220/10 C08F 220/10 (56) References JP1 JP-10-235 (JP, A) JP-A-59-125726 (JP, A) JP-A-2-208343 (JP, A) JP-A-2-161442 (JP, A) JP-A-62-24246 (JP, A) JP-A-52-94388 (JP, A) JP-A-2-154264 (JP, A) JP-A-2-43552 (JP, A) JP-A-62-74912 (JP, A) JP-A-56-1979 19752 (JP, A) (58) Fields investigated (Int. Cl. ⁶ , DB name) C08F 290/00-290/06 C08F 299/00-299/02 G03F 7/004 G03F 7/027 G03F 7/033

Claims (4)

(57) [Claims] (A) α, having 3 to 15 carbon atoms,
15 to 35% by weight of a first polymerizable substance comprising one or more compounds of a β-unsaturated carboxyl group-containing monomer; Wherein R ₁ is H, an alkyl group having 1 to 6 carbon atoms or a halogen atom, and one or more compounds selected from the group consisting of ring-substituted derivatives thereof. (2) 2 to 25% by weight of a polymerizable substance, one selected from the group consisting of an alkyl acrylate having an alkyl group having 1 to 8 carbon atoms and a hydroxyalkyl acrylate having a hydroxyalkyl group having 2 to 8 carbon atoms or 10 to 40% by weight of a third polymerizable substance comprising a further compound, wherein the alkyl group comprises alkyl methacrylate having 1 to 8 carbon atoms and the hydroxyalkyl group comprises hydroxyalkyl methacrylate having 2 to 8 carbon atoms. A fourth polymerizable material consisting of one or more compounds selected from the group, copolymerized with 30 to 65% by weight 40 to 70 parts by weight of a thermoplastic polymer for a binder, (b) a general formula [II] (Wherein R ₂ is an alkylene group having 3 to 6 carbon atoms,
R ₃ and R ₄ are H or CH ₃ , and n is a positive integer such as 5 to 9) wherein at least one ethylenic compound is contained in one molecule containing 51 to 100% by weight of a compound represented by the formula: Crosslinkable monomer 25 having an unsaturated group
(C) 0 to 10 parts by weight of the photopolymerization initiator in a total amount of 100 parts by weight.
A crosslinked curable resin composition which is combined so as to be parts by weight. 2. A crosslinkable monomer (b) having one or more ethylenically unsaturated groups in one molecule is represented by the general formula [III]: Wherein R ₃ and R ₄ are H or CH ₃ , and n is a positive integer such as 5-9.
Claim 1 characterized by containing 0% by weight.
The cross-linking-curable resin composition according to the item. 3. The cross-linkable resin composition according to claim 2, wherein the number of oxypropylene repeating units of the compound represented by the general formula [III] is n = 7. 4. The method according to claim 1, wherein the tetrazole or a derivative thereof is (a) +
4. The cross-linking curable resin composition according to claim 1, wherein the content is 0.005 to 5 parts by weight based on 100 parts by weight of (b) + (c).