JPH01237132A - Manufacture of heat-curable resin copper-clad laminate - Google Patents
Manufacture of heat-curable resin copper-clad laminateInfo
- Publication number
- JPH01237132A JPH01237132A JP6316388A JP6316388A JPH01237132A JP H01237132 A JPH01237132 A JP H01237132A JP 6316388 A JP6316388 A JP 6316388A JP 6316388 A JP6316388 A JP 6316388A JP H01237132 A JPH01237132 A JP H01237132A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- heat
- fiber paper
- copper
- dried
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 35
- 239000011347 resin Substances 0.000 title claims abstract description 35
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000011889 copper foil Substances 0.000 claims abstract description 20
- 239000005011 phenolic resin Substances 0.000 claims abstract description 14
- 229920006231 aramid fiber Polymers 0.000 claims abstract description 13
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims abstract description 10
- 238000001035 drying Methods 0.000 claims abstract description 9
- 239000002966 varnish Substances 0.000 claims abstract description 6
- 238000010030 laminating Methods 0.000 claims abstract description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000000123 paper Substances 0.000 abstract description 13
- 239000003822 epoxy resin Substances 0.000 abstract description 10
- 229920000647 polyepoxide Polymers 0.000 abstract description 10
- 238000005476 soldering Methods 0.000 abstract description 8
- 239000000835 fiber Substances 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 4
- 229920000271 Kevlar® Polymers 0.000 abstract description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 239000004761 kevlar Substances 0.000 abstract description 2
- 229920001225 polyester resin Polymers 0.000 abstract description 2
- 239000004645 polyester resin Substances 0.000 abstract description 2
- 239000007767 bonding agent Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 description 14
- 239000000853 adhesive Substances 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 10
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920003987 resole Polymers 0.000 description 3
- 229910000679 solder Inorganic materials 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 229920001494 Technora Polymers 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000004950 technora Substances 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 229920003261 Durez Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000011101 paper laminate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- -1 polyparaphenylene terephthalamide Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Manufacturing Of Printed Wiring (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、耐熱性、銅箔引きはがし強度に優れたアラミ
ド繊維紙基材銅張積N仮の製造方法に関するものである
。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing a copper-clad N temporary aramid fiber paper base having excellent heat resistance and copper foil peeling strength.
〔従来技術]
従来、アラミド繊維紙積層板は、低熱膨張のため表面実
装用基板として一部使用されているが、はんだ耐熱性が
十分ではないという欠点があり、その改良が望まれてい
た。[Prior Art] Conventionally, aramid fiber paper laminates have been partially used as substrates for surface mounting due to their low thermal expansion, but they have the drawback of insufficient solder heat resistance, and an improvement has been desired.
また、基材のアラミド繊維が樹脂を吸引しやすく、基材
表面に樹脂が少ないため、w4箔との接着性が劣ってい
た。In addition, the aramid fibers of the base material easily absorbed resin, and since there was little resin on the surface of the base material, the adhesion to the W4 foil was poor.
本発明者は、従来のアラミド繊維紙基材の熱硬化性樹脂
積層板のはんだ耐熱性9銅箔引きはがし強度が低いとい
う欠点を解決するため、プリプレグ中の揮発成分を低下
し、かつフェノール樹脂とポリビニルブチラールからな
る樹脂を銅箔接着剤に使用することにより、はんだ耐熱
性、銅箔引はがし強度を著しく向上させうることを見出
し、本発明を完成するに至った。In order to solve the drawback of low soldering heat resistance 9 copper foil peeling strength of conventional thermosetting resin laminates based on aramid fiber paper, the present inventors reduced the volatile components in the prepreg and developed a method using phenolic resin. The present inventors have discovered that the soldering heat resistance and copper foil peel strength can be significantly improved by using a resin consisting of polyvinyl butyral and polyvinyl butyral in a copper foil adhesive, and have completed the present invention.
〔発明の構成]
本発明は、熱硬化性樹脂からなるワニスをアラミド繊維
1維祇からなる基材に含浸乾燥して揮発成分を1.5%
以下にコントロールしたプリプレグの−枚ないし複数枚
と、フェノール樹脂とポリビニルブチラール樹脂を主成
分とする樹脂接着剤を塗工乾燥した銅箔とを積層し加熱
加圧することを特徴とする熱硬化性樹脂銅張積層板の製
造方法に関するものである。[Structure of the Invention] The present invention impregnates a base material made of aramid fiber 1 fiber with a varnish made of thermosetting resin and dries it to reduce the volatile component to 1.5%.
A thermosetting resin characterized by laminating one or more sheets of prepreg controlled as follows and copper foil coated and dried with a resin adhesive mainly composed of phenol resin and polyvinyl butyral resin and then heated and pressed. The present invention relates to a method for manufacturing a copper-clad laminate.
本発明でいう熱硬化性樹脂は、エポキシ樹脂、フェノー
ル樹脂、ポリイミド樹脂、ポリエステル樹脂などであり
、そのいずれにも限定されない。The thermosetting resin referred to in the present invention includes epoxy resin, phenol resin, polyimide resin, polyester resin, etc., and is not limited to any of them.
アラミド繊維紙には、ポリパラフェニレンテレフタラミ
ド(PPT^)の構造を持つケブラーのを用いたケプラ
ー繊維紙と、ポリバラフェニレン−3゜4−ジフェニル
エーテルテレフタラミドの構造を持つテクノーラ0を用
いたテクノーラ繊維紙がある。For the aramid fiber paper, we used Kevlar fiber paper with a structure of polyparaphenylene terephthalamide (PPT^) and Technora 0 with a structure of polyparaphenylene-3゜4-diphenyl ether terephthalamide. There is Technora fiber paper.
本発明において使用する銅箔接着剤は、フェノール樹脂
とポリビニルブチラール樹脂とを主成分とした樹脂であ
るが、エポキシ樹脂、メラミン樹脂及び他の添加剤を加
えてもよい。The copper foil adhesive used in the present invention is a resin mainly composed of phenol resin and polyvinyl butyral resin, but epoxy resin, melamine resin, and other additives may be added.
本発明において、揮発成分の値はプリプレグをJツ
200°C,19分間乾燥し、乾燥前後の重量を標定し
、次式によって算出される。In the present invention, the value of volatile components is calculated by drying the prepreg at 200° C. for 19 minutes, determining the weight before and after drying, and using the following formula.
本発明に使用されるプリプレグは揮発成分が1.5%以
下、好ましくは0.6%以下のものである。The prepreg used in the present invention has a volatile component content of 1.5% or less, preferably 0.6% or less.
本発明の特徴のひとつはアラミド繊維紙プリプレグ中の
揮発成分の割合を1.5重量%以下とする点であるが、
1.5%以上でははんだ耐熱性向上の効果が小さい、0
.6%以下の場合、はんだ耐熱性向上効果がより石育実
なものとなり、通常のガラスエポキシ積層板と同等にな
る。One of the features of the present invention is that the proportion of volatile components in the aramid fiber paper prepreg is 1.5% by weight or less,
At 1.5% or more, the effect of improving soldering heat resistance is small;
.. When it is 6% or less, the effect of improving soldering heat resistance becomes more significant and becomes equivalent to that of a normal glass epoxy laminate.
また、プリプレグの揮発成分を低くするための乾燥は樹
脂の硬化反応が進まない範囲で高温長時間が望ましいが
通常80°C〜120°C12〜20分程度である。In order to reduce the volatile components of the prepreg, drying is preferably carried out at a high temperature for a long period of time within a range where the curing reaction of the resin does not progress, but it is usually 80°C to 120°C for about 12 to 20 minutes.
プリプレグの揮発成分を低くする方法には、プリプレグ
を再度乾燥する方法の他、プリプレグをワニス含浸乾燥
後低湿度下で保管する方法、プリプレグを真空状態にし
て成形する方法などが考えられる。Possible methods for reducing the volatile components of prepreg include drying the prepreg again, storing the prepreg in a low humidity environment after impregnating it with varnish and drying it, and molding the prepreg under vacuum.
本発明のもうひとつの特徴は、フェノール樹脂とポリビ
ニルブチラール樹脂とを主成分とした銅箔接着剤を使用
する点である。Another feature of the present invention is the use of a copper foil adhesive whose main components are phenolic resin and polyvinyl butyral resin.
フェノール樹脂にはレゾール型樹脂とノボラック型用脂
があるが、本発明にはレゾール型閘脂の使用が好ましい
、尚レゾール型樹脂の反応触媒には、アンモニア、水酸
化バリウム、酸化マグネシウム等が好ましく使用される
。フェノール樹脂は数平均分子量が200から400の
範囲で使用出来るが、好ましくは250から350の範
囲である。Phenol resins include resol type resins and novolac type resins, but in the present invention, it is preferable to use resol type resins. In addition, ammonia, barium hydroxide, magnesium oxide, etc. are preferable as reaction catalysts for resol type resins. used. The phenol resin can be used with a number average molecular weight in the range of 200 to 400, but preferably in the range of 250 to 350.
一方、ポリビニルブチラールは重合度が500から50
00の範囲のものが使用できるが、好ましくは800か
ら4000の範囲である。ブチラール化度については特
に限定されるものでないが、bfマしくは55から70
モル%である。On the other hand, polyvinyl butyral has a polymerization degree of 500 to 50.
A range of 0.00 can be used, but a range of 800 to 4000 is preferred. The degree of butyralization is not particularly limited, but bf is preferably 55 to 70.
It is mole%.
エポキシ樹脂にはエポキシ当量が350から′?00の
範囲のものが使用できるか、好ましくは、100から5
00の範囲である。Epoxy resin has an epoxy equivalent weight of 350 to '? 00 range can be used, preferably 100 to 5
The range is 00.
樹脂の配合割合はフェノ−・ル樹脂30重量部′固形分
)から80重量部(固形分)とポリビニ・1ブナラ一ル
70重1部(固形分)から20重量部(固形分)の範囲
で配合した樹脂100重量部(固形分)にエポキシ樹脂
5重1部(固形分)から25重量部(固形分)の配合範
囲が使用できるが、好ましくはフェノール樹脂40重量
部(固形分)から75重量部(固形分)とポリビニルブ
チラール60重量部(固形分)から25重量部(固形分
)の範囲で配合した樹脂100重量部(固形分)にエポ
キシ樹脂5重量部(固形分)から25重量部(固形分)
の配合範囲である。The blending ratio of the resins ranges from 30 parts by weight (solid content) to 80 parts by weight (solid content) for phenolic resin and 1 part by weight (solid content) to 1 part by weight (solid content) for polyvinyl resin. A blending range of from 5 parts by weight of epoxy resin to 1 part by weight (solid content) to 25 parts by weight (solid content) to 100 parts by weight (solid content) of the resin blended in can be used, but preferably from 40 parts by weight (solid content) to phenolic resin. 75 parts by weight (solid content) and polyvinyl butyral in a range of 60 parts by weight (solid content) to 25 parts by weight (solid content) to 100 parts by weight (solid content) of an epoxy resin and 5 parts by weight (solid content) to 25 parts by weight of an epoxy resin. Part by weight (solid content)
This is the blending range of
本発明の熱硬化性樹脂銅張積層板の製造方法には次のよ
うな特長がある。The method for manufacturing a thermosetting resin copper-clad laminate according to the present invention has the following features.
(1)従来より揮発成分の低いプリプレグを使用するこ
とにより、はんだ耐熱性を著しく向上させた。(1) By using a prepreg with lower volatile components than before, the soldering heat resistance has been significantly improved.
(11)銅笛接″4剤を使用することにより、銅箔引き
はがし強度も著しく向上させた。(11) By using the copper foil welding agent 4, the peeling strength of the copper foil was also significantly improved.
〔実施例] 以下に本発明の実施例および比較例(従末例)を示す。〔Example] Examples of the present invention and comparative examples (subordinate examples) are shown below.
実施例
熱硬化性樹脂として、ここではエポキシ樹脂を使用した
。EXAMPLE An epoxy resin was used here as the thermosetting resin.
エポキシ樹脂(油化シェル類 EP−1001)100
部
ジシアンアミド 42−フェニル
−4−メチルセロソル
ブ板15
メチルセロソルブ 36アセトン
60上記材料を混合して均一
なワニスを得た。このワニスをアラミド繊維紙に含浸し
、165°C〜175°C5分間乾燥し、アラミド繊維
紙プリプレグを得た。Epoxy resin (oiled shells EP-1001) 100
dicyanamide 42-phenyl-4-methyl cellosolve board 15 methyl cellosolve 36 acetone
60 The above materials were mixed to obtain a uniform varnish. Aramid fiber paper was impregnated with this varnish and dried at 165°C to 175°C for 5 minutes to obtain an aramid fiber paper prepreg.
上記プリプレグをさらに100°Cで約10分乾燥し、
揮発成分1.5%以下のプリプレグを得た。The above prepreg was further dried at 100°C for about 10 minutes,
A prepreg containing volatile components of 1.5% or less was obtained.
さらにこのプリプレグを全層配置し、その上に下記の接
着剤付銅箔を重ね、165℃、60kg/d、90分加
熱成形して厚さ1.6 ffl1lO銅張積層板を得た
。Further, all layers of this prepreg were arranged, and a copper foil with adhesive described below was layered thereon, and heat molded at 165° C., 60 kg/d, for 90 minutes to obtain a copper-clad laminate having a thickness of 1.6 ffl11O.
銅箔接着剤の配合は次のと今りである。The composition of the copper foil adhesive is as follows.
と+4
ポリ中子≠ルプチラール(積木化学製BX−1)80部
メチルエチルケトン 650フエノール樹
脂(住友デュレズ製PR−51406)エポキシ樹脂(
油化シェル類EP−tool)上記接着剤を銅箔の粗化
面上に厚さ30〜40μ11塗布し、風乾後150℃乾
燥器中で4分乾燥し、接着剤付銅箔を作成した。and +4 Poly core ≠ Lupetiral (BX-1 manufactured by Block Chemical) 80 parts Methyl ethyl ketone 650 phenol resin (PR-51406 manufactured by Sumitomo Durez) Epoxy resin (
Oilified shells EP-tool) The above adhesive was applied to a thickness of 30 to 40 μl on the roughened surface of the copper foil, air-dried, and then dried in a dryer at 150° C. for 4 minutes to create an adhesive-coated copper foil.
比較例1
実施例と同様にしてプリプレグを得、追加の乾燥をしな
いでそのまま積層しwA箔は接着剤を塗布しないで重ね
、実施例1と同様の条件で積層し銅張積層板を得た。Comparative Example 1 Prepreg was obtained in the same manner as in Example, and laminated as is without additional drying. wA foil was laminated without applying adhesive, and laminated under the same conditions as in Example 1 to obtain a copper-clad laminate. .
比較例2
実施例と同様にしてプリプレグを得、100°Cで約1
0分乾燥し、揮発成分1.5%以下のプリプレグを得た
。このプリプレグの複数枚を積層し、銅箔は接着剤を塗
布しないで重ね、実施例1と同様の条件で銅張積層板を
得た。Comparative Example 2 A prepreg was obtained in the same manner as in the example, and at 100°C
After drying for 0 minutes, a prepreg containing volatile components of 1.5% or less was obtained. A plurality of sheets of this prepreg were laminated, and the copper foils were stacked without applying an adhesive to obtain a copper-clad laminate under the same conditions as in Example 1.
以上の各個によって得られた銅張積層板について、JI
S C6481によるはんだ耐熱性及び銅張引きはがし
強度の測定結果を表−1に示す。Regarding the copper-clad laminates obtained by each of the above, JI
Table 1 shows the measurement results of solder heat resistance and copper tensile peel strength using SC6481.
表1 銅箔用はがし強度とはんだ耐熱性以上のように、
本発明における熱硬化性樹脂銅張積層板は銅箔用はがし
強度、はんだ耐熱性ともに著しくすぐれた積層板である
。Table 1 Peeling strength and soldering heat resistance for copper foil As shown above,
The thermosetting resin copper-clad laminate according to the present invention is a laminate having extremely excellent peel strength for copper foil and solder heat resistance.
Claims (1)
らなる基材に含浸乾燥して揮発成分を1.5重量%以下
にコントロールしたプリプレグの一枚ないし複数枚と、
フェノール樹脂とポリビニルブチラール樹脂を主成分と
する樹脂をあらかじめ塗工乾燥した銅箔とを積層して加
熱加圧することを特徴とする熱硬化性樹脂銅張積層板の
製造方法。(1) One or more sheets of prepreg prepared by impregnating and drying a base material made of aramid fiber paper with a varnish made of a thermosetting resin and controlling the volatile components to 1.5% by weight or less;
A method for producing a thermosetting resin copper-clad laminate, which comprises laminating copper foil coated and dried in advance with a resin whose main components are phenol resin and polyvinyl butyral resin, and heating and pressurizing the laminated sheets.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6316388A JPH01237132A (en) | 1988-03-18 | 1988-03-18 | Manufacture of heat-curable resin copper-clad laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6316388A JPH01237132A (en) | 1988-03-18 | 1988-03-18 | Manufacture of heat-curable resin copper-clad laminate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01237132A true JPH01237132A (en) | 1989-09-21 |
Family
ID=13221298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6316388A Pending JPH01237132A (en) | 1988-03-18 | 1988-03-18 | Manufacture of heat-curable resin copper-clad laminate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01237132A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04144187A (en) * | 1990-10-04 | 1992-05-18 | Hitachi Chem Co Ltd | Copper-clad laminated board |
JPH06268345A (en) * | 1992-05-06 | 1994-09-22 | Matsushita Electric Ind Co Ltd | Circuit forming board and production thereof |
-
1988
- 1988-03-18 JP JP6316388A patent/JPH01237132A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04144187A (en) * | 1990-10-04 | 1992-05-18 | Hitachi Chem Co Ltd | Copper-clad laminated board |
JPH06268345A (en) * | 1992-05-06 | 1994-09-22 | Matsushita Electric Ind Co Ltd | Circuit forming board and production thereof |
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