JPH04239535A - Resin composition for laminated plate - Google Patents
Resin composition for laminated plateInfo
- Publication number
- JPH04239535A JPH04239535A JP679491A JP679491A JPH04239535A JP H04239535 A JPH04239535 A JP H04239535A JP 679491 A JP679491 A JP 679491A JP 679491 A JP679491 A JP 679491A JP H04239535 A JPH04239535 A JP H04239535A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- resin composition
- formula
- thermosetting resin
- curing agent
- 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
- 239000011342 resin composition Substances 0.000 title claims abstract description 12
- 229920005989 resin Polymers 0.000 claims abstract description 25
- 239000011347 resin Substances 0.000 claims abstract description 25
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract description 6
- 239000003795 chemical substances by application Substances 0.000 abstract description 5
- 239000003822 epoxy resin Substances 0.000 abstract description 5
- 229920000647 polyepoxide Polymers 0.000 abstract description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 4
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003063 flame retardant Substances 0.000 abstract description 3
- 238000006116 polymerization reaction Methods 0.000 abstract description 3
- 229910000410 antimony oxide Inorganic materials 0.000 abstract description 2
- 150000004982 aromatic amines Chemical class 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 abstract description 2
- 238000010526 radical polymerization reaction Methods 0.000 abstract description 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 238000005452 bending Methods 0.000 abstract 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000002966 varnish Substances 0.000 description 8
- 229920003986 novolac Polymers 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 239000011889 copper foil Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- ZOQVDXYAPXAFRW-UHFFFAOYSA-N 2,5-diethyl-1h-imidazole Chemical compound CCC1=CNC(CC)=N1 ZOQVDXYAPXAFRW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 229920006380 polyphenylene oxide Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- 208000037062 Polyps Diseases 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000002496 iodine Chemical class 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920006113 non-polar polymer Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/032—Organic insulating material consisting of one material
- H05K1/0326—Organic insulating material consisting of one material containing O
Landscapes
- Reinforced Plastic Materials (AREA)
- Epoxy Resins (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、高周波領域での使用に
適した電気絶縁用積層板製造用の熱硬化性樹脂組成物に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermosetting resin composition for producing electrically insulating laminates suitable for use in the high frequency range.
【0002】0002
【従来の技術】従来、ガラス織布等のシート状基材にエ
ポキシ樹脂やポリイミド樹脂を含浸、乾燥して得たプリ
プレグを所定枚数重ね、これを加熱加圧成形した積層板
がプリント配線板の絶縁基板として用いられている。そ
の誘電率は、4.9〜5.1と大きいため、プリント配
線板の静電容量が大きく、高周波数を取り扱う用途には
不向きであった。[Prior Art] Conventionally, a predetermined number of prepregs obtained by impregnating and drying a sheet-like base material such as a glass woven cloth with an epoxy resin or polyimide resin are stacked, and then the laminates are heated and pressed to form a laminate, which is used as a printed wiring board. Used as an insulating substrate. Since its dielectric constant is as large as 4.9 to 5.1, the capacitance of the printed wiring board is large, making it unsuitable for applications that handle high frequencies.
【0003】高周波領域で使用するプリント配線板には
、誘電率や誘電正接の低いものが要求され、このような
用途には、ポリフェニレンオキサイド等の耐熱性の熱可
塑性樹脂が用いられている。しかし、熱可塑性樹脂であ
ることから、耐熱性は不十分であり、半田付け工程での
寸法安定性が悪い。Printed wiring boards used in high frequency ranges are required to have low dielectric constants and dielectric loss tangents, and heat-resistant thermoplastic resins such as polyphenylene oxide are used for such applications. However, since it is a thermoplastic resin, it has insufficient heat resistance and poor dimensional stability during the soldering process.
【0004】0004
【発明が解決しようとする課題】本発明が解決しようと
する課題は、耐熱性、誘電特性のよい積層板を製造する
のに適した樹脂組成物を提供することである。SUMMARY OF THE INVENTION An object of the present invention is to provide a resin composition suitable for producing a laminate having good heat resistance and dielectric properties.
【0005】[0005]
【課題を解決するための手段】上記課題を解決するため
に、本発明に係る積層板用樹脂組成物は、樹脂成分とし
て、次の(式1)で示される熱硬化性樹脂を含むことを
特徴とする。[Means for Solving the Problems] In order to solve the above problems, the resin composition for laminates according to the present invention contains a thermosetting resin represented by the following (Formula 1) as a resin component. Features.
【0006】[0006]
【化2】[Case 2]
【0007】式中、主鎖のRとベンゼン環に結合してい
るRは、同じであっても異なっていてもよい。この樹脂
組成物をシート状基材に含浸、乾燥して得たプリプレグ
を積み重ねて加熱加圧成形し、積層板とする。In the formula, R in the main chain and R bonded to the benzene ring may be the same or different. The prepregs obtained by impregnating a sheet-like base material with this resin composition and drying are stacked and molded under heat and pressure to form a laminate.
【0008】[0008]
【作用】(式1)で示された化合物は、次の(式2)で
示される化合物をラジカル重合やイオン重合することに
より得られる。無極性高分子であるポリスチレンは吸水
率が低く誘電率、誘電正接が小さい材料であるが、本発
明に係る樹脂成分は、これにグリシジルエーテル基が共
存したポリスチレン系樹脂であるために、誘電率、誘電
正接が小さく耐熱性に優れた積層板を成形することがで
きる。[Operation] The compound represented by the formula (1) can be obtained by radical polymerization or ionic polymerization of the compound represented by the following formula (2). Polystyrene, which is a nonpolar polymer, is a material with a low water absorption rate and a small dielectric constant and dielectric loss tangent. However, the resin component according to the present invention is a polystyrene-based resin in which glycidyl ether groups coexist, so the dielectric constant is low. , it is possible to form a laminate with a small dielectric loss tangent and excellent heat resistance.
【0009】[0009]
【化3】[Chemical formula 3]
【0010】0010
【実施例】(式2)で示された化合物を重合させる場合
、スチレン、ブタジエン、イソプレンなどのビニルモノ
マと共重合させてもよい。EXAMPLES When the compound represented by formula 2 is polymerized, it may be copolymerized with a vinyl monomer such as styrene, butadiene, or isoprene.
【0011】(式1)で示される樹脂成分は、他のビス
フェノールA型グリシジルエーテルやフェノールノボラ
ック型グリシジルエーテル、クレゾールノボラック型グ
リシジルエーテル、などのエポキシ樹脂と併用してもよ
い。硬化剤は、芳香族アミン系、ジシアンジアミド、フ
ェノール樹脂系などである。フェノール樹脂系としては
、ターシャリーブチルフェノールノボラック樹脂、クレ
ゾールノボラック樹脂、ポリp−ビニルフェノール樹脂
などの使用が良好である。製造する積層板に難燃性をも
たせるために、樹脂組成物中にはハロゲン含有有機化合
物や酸化アンチモンなどの難燃剤を配合してもよい。
また、充填材、着色剤などを適宜配合してもよい。The resin component represented by formula 1 may be used in combination with other epoxy resins such as bisphenol A type glycidyl ether, phenol novolac type glycidyl ether, and cresol novolac type glycidyl ether. The curing agent is aromatic amine type, dicyandiamide, phenol resin type, etc. As the phenolic resin, tertiary butylphenol novolac resin, cresol novolac resin, polyp-vinylphenol resin, etc. are preferably used. In order to impart flame retardancy to the produced laminate, a flame retardant such as a halogen-containing organic compound or antimony oxide may be added to the resin composition. In addition, fillers, colorants, etc. may be added as appropriate.
【0012】実施例1〜2
p−イソプロペニルグリシジルエーテルを、重合開始剤
として水素化ヨウ素/ヨウ素を使用して、−40℃で1
時間重合反応を行わせた。そして、分子量3000の重
合物Aを得た。重合物Aに、フェノールノボラック樹脂
(硬化剤)、テトラブロモビスフェノールA(難燃剤)
、2−エチル−4−エチルイミダゾール(硬化促進剤)
を表1に示した割合で配合した樹脂組成物をメチルエチ
ルケトンに溶解して樹脂ワニスとした。Examples 1-2 p-isopropenyl glycidyl ether was reacted with hydrogenated iodine/iodine as a polymerization initiator at -40°C.
The polymerization reaction was carried out for a period of time. Then, a polymer A having a molecular weight of 3000 was obtained. Polymer A, phenol novolak resin (curing agent), tetrabromobisphenol A (flame retardant)
, 2-ethyl-4-ethylimidazole (hardening accelerator)
A resin composition blended in the proportions shown in Table 1 was dissolved in methyl ethyl ketone to prepare a resin varnish.
【0013】上記樹脂ワニスをガラス織布に含浸、乾燥
して、樹脂含有量42重量%のプリプレグを作製した。
このプリプレグを8枚重ね、その両表面に35μ厚さの
電解銅箔を配置して、160℃、50Kg/cm2で3
0分間加熱加圧成形して、1.6mm厚さの銅張り積層
板を得た。その特性を表1に併せて示した。A glass woven fabric was impregnated with the above resin varnish and dried to produce a prepreg having a resin content of 42% by weight. Eight sheets of this prepreg were stacked, electrolytic copper foil with a thickness of 35μ was placed on both surfaces, and
A copper-clad laminate having a thickness of 1.6 mm was obtained by heat-pressing molding for 0 minutes. Its characteristics are also shown in Table 1.
【0014】実施例3
実施例1で使用した樹脂ワニスをガラス不織布に含浸、
乾燥して、樹脂含有量88重量%のプリプレグを作製し
た。このプリプレグ3枚の両側に、実施例1で使用した
ガラス織布プリプレグを1枚ずつ重ね、さらに両表面に
35μ厚さの電解銅箔を配置して、実施例1と同様に加
熱加圧成形して、1.6mm厚さの銅張り積層板を得た
。
その特性を表1に併せて示した。Example 3 A glass nonwoven fabric was impregnated with the resin varnish used in Example 1.
It was dried to produce a prepreg with a resin content of 88% by weight. The glass woven fabric prepreg used in Example 1 was stacked one by one on both sides of these three prepregs, and electrolytic copper foil with a thickness of 35μ was placed on both surfaces, followed by heating and pressure molding in the same manner as in Example 1. As a result, a copper-clad laminate having a thickness of 1.6 mm was obtained. Its characteristics are also shown in Table 1.
【0015】実施例4
α−メチルスチリルグリシジルエーテルを、重合開始剤
として水素化ヨウ素/ヨウ素を使用して、−40℃で1
時間重合反応を行わせた。そして、分子量3500の重
合物Bを得た。重合物B、フェノールノボラック樹脂(
硬化剤)、2−エチル−4−エチルイミダゾール(硬化
促進剤)を表1に示した割合で配合した樹脂組成物をメ
チルエチルケトンに溶解して樹脂ワニスとした。Example 4 α-Methystyryl glycidyl ether was reacted with iodine hydride/iodine as a polymerization initiator at -40°C.
The polymerization reaction was carried out for a period of time. Then, a polymer B having a molecular weight of 3,500 was obtained. Polymer B, phenol novolak resin (
A resin composition containing a curing agent) and 2-ethyl-4-ethylimidazole (curing accelerator) in the proportions shown in Table 1 was dissolved in methyl ethyl ketone to prepare a resin varnish.
【0016】上記樹脂ワニスをガラス織布に含浸、乾燥
して、樹脂含有量42重量%のプリプレグを作製した。
このプリプレグを8枚重ね、その両表面に35μ厚さの
電解銅箔を配置して、実施例1と同様に加熱加圧成形し
て、1.6mm厚さの銅張り積層板を得た。その特性を
表1に併せて示した。A glass woven fabric was impregnated with the above resin varnish and dried to produce a prepreg having a resin content of 42% by weight. Eight sheets of this prepreg were stacked, electrolytic copper foils with a thickness of 35 μm were placed on both surfaces, and hot and pressure molded in the same manner as in Example 1 to obtain a copper-clad laminate with a thickness of 1.6 mm. Its characteristics are also shown in Table 1.
【0017】従来例1
エポキシ樹脂(エポキシ当量:500,油化シエル製E
p−1001)80重量部、クレゾールノボラックエポ
キシ樹脂(エポキシ当量:210,東都化成製YDCN
−704)20重量部、ジシアンジアミド4重量部、2
−エチル4−メチルイミダゾール0.2重量部をメチル
エチルケトンに溶解して樹脂ワニスとした。この樹脂ワ
ニスを使用して、以下、実施例1と同様に加熱加圧成形
して、1.6mm厚さの銅張り積層板を得た。その特性
を表1に併せて示した。Conventional Example 1 Epoxy resin (epoxy equivalent: 500, manufactured by Yuka Ciel E)
p-1001) 80 parts by weight, cresol novolak epoxy resin (epoxy equivalent: 210, YDCN manufactured by Toto Kasei)
-704) 20 parts by weight, dicyandiamide 4 parts by weight, 2
A resin varnish was prepared by dissolving 0.2 parts by weight of -ethyl 4-methylimidazole in methyl ethyl ketone. Using this resin varnish, heat and pressure molding was carried out in the same manner as in Example 1 to obtain a copper-clad laminate having a thickness of 1.6 mm. Its characteristics are also shown in Table 1.
【0018】従来例2
変性ポリフェニレンオキサイドをトリクロロエチレンに
溶解した樹脂ワニスを、ガラス織布に含浸、乾燥して、
樹脂含有量42重量%のプリプレグを作製した。以下、
実施例1と同様に加熱加圧成形して、1.6mm厚さの
銅張り積層板を得た。その特性を表1に併せて示した。Conventional Example 2 A glass woven cloth was impregnated with a resin varnish prepared by dissolving modified polyphenylene oxide in trichlorethylene, and dried.
A prepreg with a resin content of 42% by weight was produced. below,
A copper-clad laminate having a thickness of 1.6 mm was obtained by heat-pressing molding in the same manner as in Example 1. Its characteristics are also shown in Table 1.
【0019】[0019]
【表1】[Table 1]
【0020】表1における特性試験の方法は、次の通り
である。
銅箔ピール強度:JIS−C−6481に準拠半田耐熱
:積層板を280℃の半田浴に浮かべ、表面にふくれが
発生するまでの時間を測定
難燃性:UL−94に準拠The method of characteristic testing in Table 1 is as follows. Copper foil peel strength: Compliant with JIS-C-6481 Solder heat resistance: Float the laminate in a solder bath at 280°C and measure the time until blistering occurs on the surface Flame retardancy: Compliant with UL-94
【0021】[0021]
【発明の効果】上述のように、本発明に係る樹脂組成物
を使用することにより、誘電率、誘電正接が小さく耐熱
性に優れた積層板を成形することができる。高周波特性
を扱うプリント配線板の製造用として適したものである
。As described above, by using the resin composition of the present invention, it is possible to mold a laminate having a small dielectric constant and a small dielectric loss tangent and excellent heat resistance. It is suitable for manufacturing printed wiring boards that handle high frequency characteristics.
Claims (1)
化性樹脂を含む積層板用樹脂組成物。 【化1】1. A resin composition for a laminate comprising a thermosetting resin represented by the formula (1) as a resin component. [Chemical formula 1]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP679491A JPH04239535A (en) | 1991-01-24 | 1991-01-24 | Resin composition for laminated plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP679491A JPH04239535A (en) | 1991-01-24 | 1991-01-24 | Resin composition for laminated plate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04239535A true JPH04239535A (en) | 1992-08-27 |
Family
ID=11648083
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP679491A Pending JPH04239535A (en) | 1991-01-24 | 1991-01-24 | Resin composition for laminated plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04239535A (en) |
-
1991
- 1991-01-24 JP JP679491A patent/JPH04239535A/en active Pending
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