JPH04358805A - Manufacture of prepreg - Google Patents
Manufacture of prepregInfo
- Publication number
- JPH04358805A JPH04358805A JP13515591A JP13515591A JPH04358805A JP H04358805 A JPH04358805 A JP H04358805A JP 13515591 A JP13515591 A JP 13515591A JP 13515591 A JP13515591 A JP 13515591A JP H04358805 A JPH04358805 A JP H04358805A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- prepreg
- inorganic filler
- nonwoven fabric
- coating
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000011347 resin Substances 0.000 claims abstract description 36
- 229920005989 resin Polymers 0.000 claims abstract description 36
- 239000002966 varnish Substances 0.000 claims abstract description 15
- 239000011256 inorganic filler Substances 0.000 claims abstract description 14
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 14
- 238000001035 drying Methods 0.000 claims abstract description 12
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 6
- 239000004745 nonwoven fabric Substances 0.000 claims description 19
- 239000000463 material Substances 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 abstract description 8
- 238000000576 coating method Methods 0.000 abstract description 8
- 239000004744 fabric Substances 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 2
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 239000006260 foam Substances 0.000 abstract 1
- 239000011342 resin composition Substances 0.000 abstract 1
- 239000011521 glass Substances 0.000 description 26
- 239000002759 woven fabric Substances 0.000 description 9
- 239000010410 layer Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000011889 copper foil Substances 0.000 description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- RIAHASMJDOMQER-UHFFFAOYSA-N 5-ethyl-2-methyl-1h-imidazole Chemical compound CCC1=CN=C(C)N1 RIAHASMJDOMQER-UHFFFAOYSA-N 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は不織布を基材とするプリ
プレグの製造方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing prepreg using nonwoven fabric as a base material.
【0002】0002
【従来の技術】基材としてガラス不織布を用いたCEM
−3材は、Vカットを利用した基板の集合化ができ、配
線板加工上経済的なメリットが大きい。しかも、無機質
充填剤を含む樹脂を使用することにより、スルーホール
信頼性、そり、寸法精度等の特性において、ガラス織布
を用いたFR−4とほぼ同等の材料が得られるようにな
った。[Prior art] CEM using glass nonwoven fabric as a base material
-3 material allows the assembly of boards using V-cuts, and has a great economical advantage in processing wiring boards. Furthermore, by using a resin containing an inorganic filler, it has become possible to obtain a material that is almost equivalent to FR-4 using glass woven fabric in terms of through-hole reliability, warpage, dimensional accuracy, and other properties.
【0003】不織布はその密度が小さく、単位体積当り
に含浸される樹脂分が多くなる。このようなプリプレグ
を用いて積層板を製造すると、端部の板厚が小さくなる
。そこで、成形時の樹脂流れを抑えるため、従来は一般
のプリプレグよりも乾燥温度を高くして樹脂の硬化度を
高めていた。[0003] Nonwoven fabric has a low density, and a large amount of resin is impregnated per unit volume. When a laminate is manufactured using such prepreg, the thickness of the end portion becomes smaller. Therefore, in order to suppress resin flow during molding, conventionally the drying temperature was higher than that of general prepreg to increase the degree of curing of the resin.
【0004】0004
【発明が解決しようとする課題】樹脂の硬化度の高いプ
リプレグを使用して積層板を製造すると、中央部の樹脂
流れが少なくなり、硬化時間も短くなるため、中央部に
ボイドやかすれを生ずる。また、積層板の表層に用いる
ガラス織布基材プリプレグとの硬化度が異なるため、ガ
ラス織布基材層とガラス不織布基材層との密着が不充分
となることがあった。さらに、プリプレグ表層部の方が
内部よりも、多くの熱エネルギーを受けるため、内部に
あった空隙や、乾燥によって揮発してしまうはずの揮発
成分を内部に閉じ込んだまま表層部が先に硬化し、ボイ
ドやふくれの原因となる。[Problem to be solved by the invention] When a laminate is manufactured using a prepreg with a highly cured resin, the resin flow in the center is reduced and the curing time is shortened, resulting in voids and scratches in the center. . Further, since the degree of curing is different from that of the glass woven fabric base material prepreg used for the surface layer of the laminate, the adhesion between the glass woven fabric base material layer and the glass nonwoven fabric base material layer may be insufficient. Furthermore, since the surface layer of the prepreg receives more heat energy than the inside, the surface layer hardens first while trapping the internal voids and volatile components that would otherwise volatilize during drying. This can cause voids and blisters.
【0005】無機質の充填材を含む熱硬化性樹脂ワニス
は粘度が高いためこのような現象が顕著である。本発明
はこのような課題を解決しようとするものである。[0005] This phenomenon is conspicuous because thermosetting resin varnishes containing inorganic fillers have high viscosity. The present invention attempts to solve such problems.
【0006】[0006]
【課題を解決するための手段】本発明は、無機質の充填
材を含む熱硬化性樹脂ワニスを不織布基材に塗工し乾燥
した後、無機質の充填材を含む熱硬化性樹脂ワニスの塗
工、乾燥をさらに1回以上繰り返すことを特徴とする。[Means for Solving the Problems] The present invention provides a method for applying a thermosetting resin varnish containing an inorganic filler to a nonwoven fabric base material, drying it, and then applying a thermosetting resin varnish containing an inorganic filler. , the drying process is repeated one or more times.
【0007】本発明で用いられる樹脂は、フェノール樹
脂、エポキシ樹脂、ポリイミド樹脂、ポリエステル樹脂
等の電気絶縁板に使用されている一般の樹脂である。ま
た塗工毎の樹脂の粘度、樹脂分等の条件や乾燥条件等は
樹脂の種類に応じて、個々最適値を選ぶ。樹脂の塗工量
は好ましく初回のは最終塗工量の1/2以下とし、初回
の工程での硬化はできるだけ抑えた方が良好である。繰
返し工程数は多いほどよい結果が得られるが、製造工数
が増えるため、2〜3回がのぞましい。[0007] The resin used in the present invention is a general resin used for electrical insulating boards, such as phenol resin, epoxy resin, polyimide resin, or polyester resin. In addition, conditions such as resin viscosity, resin content, drying conditions, etc. for each coating are individually selected to be optimum values depending on the type of resin. The coating amount of the resin is preferably 1/2 or less of the final coating amount in the first step, and it is better to suppress curing in the first step as much as possible. The greater the number of repeated steps, the better the results, but because the number of manufacturing steps increases, it is preferable to repeat the steps 2 to 3 times.
【0008】[0008]
【作用】通常1回の工程で、必要な樹脂量全部を塗工し
、乾燥しているところを、2回以上の工程で行うため、
1回の工程で基材に塗工する樹脂量を少なくすることが
できる。とくに初回に塗工する樹脂量を少なくすること
によって、基材繊維の表面に樹脂の薄い膜ができ、2回
目以降の塗工において樹脂と基材の親和性が増す。
このため、基材中の空気は樹脂によって置き換えられや
すくなり、空隙の少ないプリプレグが得られる。また、
1回の工程で塗工する樹脂量を少量とすることによって
樹脂の厚みが小さくなり、乾燥工程での樹脂の表層部と
内部の硬化度の差が小さくなる。[Operation] Normally, all the required amount of resin is applied and dried in one process, but it is done in two or more processes.
The amount of resin applied to the base material in one process can be reduced. In particular, by reducing the amount of resin applied for the first time, a thin film of resin is formed on the surface of the base fiber, and the affinity between the resin and the base material increases in the second and subsequent applications. Therefore, the air in the base material is easily replaced by the resin, and a prepreg with fewer voids can be obtained. Also,
By reducing the amount of resin applied in one step, the thickness of the resin becomes smaller, and the difference in the degree of curing between the surface layer and the inside of the resin in the drying step becomes smaller.
【0009】[0009]
実施例1
積層板用ブロム化エポキシ樹脂100重量部、ジシアン
ジアミド4重量部および2−メチル−4−エチルイミダ
ゾール0.15重量部を、N,N−ジメチルホルムアミ
ド30重量部およびメチルセロソルブ30重量部からな
る溶剤に溶解した。さらに、樹脂分100重量部に対し
て水酸化アルミニウム(住友化学工業株式会社製CL−
310)を100重量部添加、撹拌した。Example 1 100 parts by weight of brominated epoxy resin for laminates, 4 parts by weight of dicyandiamide and 0.15 parts by weight of 2-methyl-4-ethylimidazole were mixed with 30 parts by weight of N,N-dimethylformamide and 30 parts by weight of methyl cellosolve. It was dissolved in a solvent. Furthermore, aluminum hydroxide (CL-
310) was added and stirred.
【0010】この無機質充填剤入りワニスを、ガラス不
織布(日本バイリーン株式会社製EPM−4060N)
に樹脂分30.0±2.0%となるように塗工し、15
0℃で3分間乾燥した。これに、樹脂分90.0±2.
0%となるように前記無機充填剤入りワニスを再度塗工
し、170℃で10分間乾燥し、ガラス不織布プリプレ
グを得た。水酸化アルミニウムを含まない外は前記ワニ
スと同じ組成のワニスをガラス布(日東紡績株式会社製
WE−18K−RB84)に樹脂分41.0±3.0%
とになるように塗工し、乾燥してガラス織布プリプレグ
を得た。[0010] This inorganic filler-containing varnish was applied to a glass nonwoven fabric (EPM-4060N manufactured by Nippon Vilene Co., Ltd.).
Coated with a resin content of 30.0±2.0%,
It was dried at 0°C for 3 minutes. In addition, the resin content was 90.0±2.
The inorganic filler-containing varnish was applied again so that the concentration was 0%, and dried at 170° C. for 10 minutes to obtain a glass nonwoven fabric prepreg. A varnish with the same composition as the above varnish except that it does not contain aluminum hydroxide is applied to glass cloth (WE-18K-RB84 manufactured by Nittobo Co., Ltd.) with a resin content of 41.0 ± 3.0%.
The glass fabric prepreg was coated and dried to obtain a glass woven fabric prepreg.
【0011】以上のようにして得られたガラス不織布プ
リプレグを3枚重ね、その上下にガラス織布プリプレグ
を重ね、最外層に厚さ18μmの電解銅箔(日本電解株
式会社製)を配置し、温度170℃、圧力2.94MP
aで70分間加熱・加圧し、厚さ1.6mmの銅張積層
板を得た。[0011] Three sheets of the glass nonwoven fabric prepreg obtained as described above were stacked, glass woven fabric prepregs were stacked above and below, and an electrolytic copper foil (manufactured by Nippon Denki Co., Ltd.) with a thickness of 18 μm was placed on the outermost layer. Temperature 170℃, pressure 2.94MP
A copper-clad laminate with a thickness of 1.6 mm was obtained by heating and pressurizing for 70 minutes.
【0012】実施例2
実施例1と同じ無機充填剤入りワニスを同じガラス不織
布に樹脂分30.0±2.0%になるように塗工し、1
50℃で3分間乾燥の後、再度樹脂分60.0±2.0
%になるように無機充填剤入りワニスを塗工し、150
℃で3分間乾燥、3回目に樹脂分90.0±2.0%に
なるように無機充填剤入りワニスを塗工し、170℃で
10分乾燥したガラス不織布プリプレグを得た。Example 2 The same inorganic filler-containing varnish as in Example 1 was applied to the same glass nonwoven fabric so that the resin content was 30.0±2.0%.
After drying at 50℃ for 3 minutes, the resin content is 60.0±2.0 again.
%, apply varnish containing inorganic filler to 150%
It was dried at 170° C. for 3 minutes, coated with an inorganic filler-containing varnish at a third time to a resin content of 90.0±2.0%, and dried at 170° C. for 10 minutes to obtain a glass nonwoven fabric prepreg.
【0013】このガラス不織布プリプレグを3枚重ね、
その上下に実施例1と同じガラス織布プリプレグを重ね
、最外層に厚さ18μmの銅箔を配置し実施例1と同じ
積層条件によって厚さ1.6mmの銅張積層板を得た。[0013] Three sheets of this glass nonwoven fabric prepreg were stacked,
The same glass woven fabric prepreg as in Example 1 was layered above and below it, and a copper foil with a thickness of 18 μm was placed as the outermost layer, and a copper-clad laminate with a thickness of 1.6 mm was obtained under the same lamination conditions as in Example 1.
【0014】比較例1
実施例1と同じ無機充填剤入りワニスを同じガラス不織
布に樹脂分90.0%になるように1回で塗工し、17
0℃で12分間乾燥しガラス不織布プリプレグを得た。Comparative Example 1 The same inorganic filler-containing varnish as in Example 1 was applied to the same glass nonwoven fabric in one coat so that the resin content was 90.0%.
It was dried at 0° C. for 12 minutes to obtain a glass nonwoven fabric prepreg.
【0015】このガラス不織布プリプレグを3枚重ね、
その上下に実施例1と同じガラス織布プリプレグを重ね
、以下実施例2と同様にして厚さ1.6mmの銅張積層
板を得た。[0015] Three sheets of this glass nonwoven fabric prepreg were stacked,
The same glass woven fabric prepreg as in Example 1 was layered on top and bottom of this, and the same procedure as in Example 2 was carried out to obtain a copper-clad laminate having a thickness of 1.6 mm.
【0016】比較例2
比較例1と同じガラス不織布プリプレグ3枚を重ね、そ
の上下にガラス織布プリプレグを重ね、最外層に厚さ1
8μmの銅箔を配置し、温度170℃、圧力5.88M
Paで70分加熱・加圧し、厚さ1.6mmの銅張積層
板を得た。以上のようにして得られた銅張積層板の特性
を表1に示す。なお、比較例1および2で得られた積層
板の中には、ガラス織布基材層とガラス不織布基材層と
の間で剥がれやすいものがあった。Comparative Example 2 Three sheets of the same glass nonwoven fabric prepreg as in Comparative Example 1 were stacked, and glass woven fabric prepregs were stacked above and below, and the outermost layer had a thickness of 1
8μm copper foil placed, temperature 170℃, pressure 5.88M
It was heated and pressurized at Pa for 70 minutes to obtain a copper-clad laminate having a thickness of 1.6 mm. Table 1 shows the properties of the copper-clad laminate obtained as described above. In addition, some of the laminates obtained in Comparative Examples 1 and 2 were prone to peeling between the glass woven fabric base material layer and the glass nonwoven fabric base material layer.
【0017】[0017]
【表1】
基板耐熱性:プレッシャークッカーテスト 121℃
0.12MPaはんだ260℃20秒ディップ[Table 1] Substrate heat resistance: Pressure cooker test 121℃
0.12MPa solder dip at 260℃ for 20 seconds
【0
018】0
018]
【発明の効果】塗工乾燥を一回で行うと成形性の良いガ
ラス不織布プリプレグを得ることができないが、二回以
上塗工し乾燥する工程を繰返すことで、ガラス不織布プ
リプレグの樹脂硬化度が平均化され成形性がよくなる。[Effect of the invention] If coating and drying is performed in one time, it is not possible to obtain a glass nonwoven fabric prepreg with good moldability, but by repeating the process of coating and drying two or more times, the degree of resin curing of the glass nonwoven fabric prepreg can be improved. It is evened out and moldability is improved.
Claims (1)
ニスを不織布基材に塗工し乾燥した後、無機質の充填材
を含む熱硬化性樹脂ワニスの塗工、乾燥をさらに1回以
上繰り返すことを特徴とするプリプレグの製造方法。Claim 1: After applying a thermosetting resin varnish containing an inorganic filler to a nonwoven fabric base material and drying, repeating the application and drying of the thermosetting resin varnish containing an inorganic filler one or more times. A prepreg manufacturing method characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13515591A JPH04358805A (en) | 1991-06-06 | 1991-06-06 | Manufacture of prepreg |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13515591A JPH04358805A (en) | 1991-06-06 | 1991-06-06 | Manufacture of prepreg |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04358805A true JPH04358805A (en) | 1992-12-11 |
Family
ID=15145102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13515591A Pending JPH04358805A (en) | 1991-06-06 | 1991-06-06 | Manufacture of prepreg |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04358805A (en) |
-
1991
- 1991-06-06 JP JP13515591A patent/JPH04358805A/en active Pending
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