JPS6225506B2 - - Google Patents
Info
- Publication number
- JPS6225506B2 JPS6225506B2 JP58198863A JP19886383A JPS6225506B2 JP S6225506 B2 JPS6225506 B2 JP S6225506B2 JP 58198863 A JP58198863 A JP 58198863A JP 19886383 A JP19886383 A JP 19886383A JP S6225506 B2 JPS6225506 B2 JP S6225506B2
- Authority
- JP
- Japan
- Prior art keywords
- base material
- laminate
- prepreg
- impregnation
- glass
- 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.)
- Expired
Links
- 239000000463 material Substances 0.000 claims description 22
- 239000004745 nonwoven fabric Substances 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- 239000011521 glass Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000010292 electrical insulation Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004744 fabric Substances 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
- 238000013007 heat curing Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 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
- H05K1/0353—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement
- H05K1/0366—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement reinforced, e.g. by fibres, fabrics
Landscapes
- Laminated Bodies (AREA)
Description
本発明は、電子機器、産業機器に用いられる積
層板の製造法に関するものであり、その目的とす
るところは基板への樹脂の均一含浸を図り、ひい
ては積層板の反りを改善し、また電気絶縁性を向
上せしめることにある。
従来、積層板に使用される基材としてガラス不
織布、ガラス−紙混抄不織布等が知られている。
該不織布は、一般的に巻物として供給され、幅方
向の端部と中央部、或は流れ方向に於て、巻きに
よる物理的力のかかり具合の違い、また含有吸湿
水分の違いがあり、樹脂含浸時の幅方向、流れ方
向の含浸ムラ、更には含浸乾燥後のプリプレグ幅
方向の端部がカールする欠点があり、該プリプレ
グを使用した積層板は端部の反りが大きく且電気
絶縁性にバラツキが生じる等の問題があつた。こ
の欠点を改善するため、含浸時樹脂稀釈溶剤を大
量に用いて低粘度含浸を行い含浸ムラを少なくす
る方法、また含浸乾燥時の基材端部のテンシヨン
調整、或は機械的に端部のカールを抑える方法等
が検討されている。しかし、前者の場合、大量の
溶剤を必要とし経済性に問題があると同時に部分
的に物理的な力を受けた変形(具体的には巻き中
央部程圧縮される)や吸湿差違(具体的には巻き
の外側及び端部程吸湿大)をカバーすることが出
来ず、ひいては積層板の反り、絶縁性の改善につ
ながらない。また、後者の場合、部分的にテンシ
ヨン調整は困難を極め、連続含浸中に基材切れ発
生の問題があり量産上不可能な方法である。
本発明はかかる欠点を改善せんとするもので、
ガラス不織布或はガラス−紙混抄不織布基材に予
め湿潤処理を行い基材の含有水分量の均一化を図
り、該基材中の含有水分量を3〜10重量%に調整
した後、熱硬化性樹脂を含浸乾燥せしめて得たプ
リプレグを使用して積層成形するものである。
本発明の詳細を一実施例をもつて説明する。
第1図に於て、ガラス不織布またはガラス−紙
混抄不織布基材2を巻物1の状態から引き出し、
水蒸気或は噴霧水発生炉3中を通過させる。この
際基材は加温した方が好ましく、また処理時間は
基材の物理的変形が緩和出来、且含有水分が均一
になるところを選択し、基材2中の水分量が3〜
10重量%になるよう調整する必要がある。3重量
%未満では充分な変形の緩和が出来ず均一水分量
の調整が困難である。また、10重量%を越えると
その後の熱硬化性樹脂含浸が経済的な含浸スピー
ドで達成出来ず電気特性の低下を招く。即ち、本
発明は、前記の如く一般的市場に於て入手し得る
ガラス不織布、ガラス−紙混抄不織布基材が運
搬、含浸量産性の点より全て巻物であり、この巻
物故の問題として提起される巻きグセ(歪)、吸
湿ムラを湿潤処理により緩和し均一化を図り、プ
リプレグの耳反り、含浸ムラをなくして、最終的
に得られる積層板の反り、電気特性を改善するも
のである。
本発明を実施するに当り使用するガラス不織布
或はガラス−紙混抄不織布としては市販のものが
使用出来る。また熱硬化性樹脂としては1段含浸
或は2段含浸で各々選択使用が可能であり、水溶
性フエノール樹脂、変性フエノール樹脂、エポキ
シ樹脂等が適用出来る。
実施例
第1図に示す如く、坪量130g/m2のガラス−
紙混抄基材2を巻物1の状態(2500m)より引き
出し、水蒸気発生炉3にて基材温度50℃で3分間
保持させ、含有水分量を7±0.5重量%に調整
後、第1含浸槽4にてメチロール化フエノール樹
脂溶液を含浸し乾燥炉7で乾燥した。更に、第2
含浸槽5にてエポキシ樹脂を含浸後乾燥炉8で乾
燥して第1表に示す特性を保持するプリプレグ6
を製造した。該プリプレグを裁断後、8ply重ね片
側に35μ厚銅箔を載置し、プレスに挿入した。圧
力80Kg/cm2、温度160℃にて60分間成形後冷却し
て1.6m/m厚の片面銅張積層板を得た。該積層
板の特性を第2表に示した。
比較例
実施例と同一の巻物1より基材2を引き出し、
第2図に示す如く該基材に湿潤処理を施す読こと
なく直接第1含浸槽4並びに第2含浸槽5に導き
実施例と同一の樹脂で同様の含浸処理を施し、第
1表に示す特性を保持するプリプレグ6′を製造
した。該プリプレグを裁断後、実施例と同様の構
成、プレス条件にて1.6m/m厚の片面銅張積層
板を得た。該積層板の特性を第2表に示した。
The present invention relates to a method for manufacturing laminates used in electronic devices and industrial equipment, and its purpose is to uniformly impregnate the substrate with resin, improve the warping of the laminate, and improve electrical insulation. The goal is to improve sexuality. Conventionally, glass nonwoven fabrics, glass-paper mixed nonwoven fabrics, and the like have been known as base materials used for laminates.
The nonwoven fabric is generally supplied as a roll, and there are differences in the extent to which physical force is applied due to the winding, as well as in the amount of moisture absorbed, between the ends and the center in the width direction, or in the machine direction. There are drawbacks such as uneven impregnation in the width direction and flow direction during impregnation, and furthermore, the ends of the prepreg in the width direction curl after impregnation and drying, and laminates using this prepreg have large warps at the ends and poor electrical insulation properties. There were problems such as variations. In order to improve this drawback, methods for reducing unevenness of impregnation by using a large amount of resin diluting solvent during impregnation to reduce impregnation unevenness, or adjusting the tension of the edges of the substrate during impregnation drying, or mechanically tightening the edges Methods to suppress curling are being considered. However, in the former case, a large amount of solvent is required and there are problems with economic efficiency, as well as deformation due to partial physical force (specifically, the central part of the winding is compressed) and moisture absorption differences (specifically, (Moisture absorption is greater at the outside and ends of the windings), which results in warpage of the laminate and does not lead to improvement in insulation. Furthermore, in the latter case, it is extremely difficult to partially adjust the tension, and there is a problem that the base material breaks during continuous impregnation, making this method impossible for mass production. The present invention aims to improve these drawbacks,
The glass nonwoven fabric or the glass-paper mixed paper nonwoven fabric base material is pre-wetted to make the moisture content of the base material uniform, and after adjusting the moisture content in the base material to 3 to 10% by weight, heat curing is performed. The material is laminated and molded using prepreg obtained by impregnating and drying a synthetic resin. The details of the present invention will be explained using an example. In FIG. 1, the glass nonwoven fabric or glass-paper mixed nonwoven fabric base material 2 is pulled out from the roll 1,
The water is passed through a steam or spray water generating furnace 3. At this time, it is preferable to heat the base material, and the treatment time is selected so that the physical deformation of the base material can be alleviated and the water content is uniform, so that the amount of water in the base material 2 is 3 to 3.
It is necessary to adjust it to 10% by weight. If it is less than 3% by weight, deformation cannot be sufficiently alleviated and it is difficult to adjust a uniform moisture content. Moreover, if it exceeds 10% by weight, the subsequent impregnation with the thermosetting resin cannot be achieved at an economical impregnation speed, resulting in a decrease in electrical properties. That is, in the present invention, the glass nonwoven fabrics and glass-paper mixed nonwoven fabric base materials available in the general market are all rolls from the viewpoint of transportation and impregnation mass production, and the problem raised because of the rolls. The purpose is to alleviate and uniformize the curling curl (distortion) and moisture absorption unevenness by wet treatment, eliminate the warping of prepreg edges and impregnation unevenness, and improve the warpage and electrical properties of the final laminate. Commercially available nonwoven glass fabrics or glass-paper mixed nonwoven fabrics can be used in carrying out the present invention. Further, the thermosetting resin can be selectively used by one-stage impregnation or two-stage impregnation, and water-soluble phenolic resins, modified phenolic resins, epoxy resins, etc. can be used. Example As shown in Figure 1, glass with a basis weight of 130 g/m 2 -
The paper mixed base material 2 is pulled out from the roll 1 (2500 m), kept at a base material temperature of 50°C for 3 minutes in a steam generating furnace 3, and after adjusting the water content to 7 ± 0.5% by weight, it is transferred to the first impregnation tank. It was impregnated with a methylolated phenol resin solution in step 4 and dried in a drying oven 7. Furthermore, the second
A prepreg 6 that is impregnated with an epoxy resin in an impregnating tank 5 and then dried in a drying oven 8 to maintain the properties shown in Table 1.
was manufactured. After cutting the prepreg, a 35 μ thick copper foil was placed on one side of the prepreg in an 8-ply layer, and the prepreg was inserted into a press. After molding for 60 minutes at a pressure of 80 kg/cm 2 and a temperature of 160° C., the molded product was cooled to obtain a single-sided copper-clad laminate having a thickness of 1.6 m/m. The properties of the laminate are shown in Table 2. Comparative example: Pull out the base material 2 from the same scroll 1 as in the example,
As shown in FIG. 2, the base material was directly led to the first impregnating tank 4 and the second impregnating tank 5 without being wetted, and was subjected to the same impregnating treatment with the same resin as in the example, and the results are shown in Table 1. A prepreg 6' was produced which retained its properties. After cutting the prepreg, a single-sided copper-clad laminate with a thickness of 1.6 m/m was obtained using the same configuration and pressing conditions as in the example. The properties of the laminate are shown in Table 2.
【表】
第1表における測定値は、それぞれ20個の試料
の測定値の最大値と最小値で示した。基材含有水
分は、実施例においては湿潤処理後の測定値であ
り、比較例においては巻物より引き出し後の測定
値である。また、プリプレグ耳部のカールは、基
材幅方向における端部の浮き上り量を測定した。[Table] The measured values in Table 1 are shown as the maximum and minimum values of the measured values of 20 samples, respectively. The moisture contained in the base material is a measured value after the wet treatment in Examples, and a measured value after being pulled out from the roll in Comparative Examples. Moreover, the curl of the prepreg edge portion was determined by measuring the amount of lift of the end portion in the width direction of the base material.
【表】
第2表における測定値は、それぞれ20個の試料
の測定値の最大値と最小値で示した。反り量Aは
1000×1000mmの積層板の角部から切り出した330
×330mmの試料片の中央部の浮き上り量を測定し
たものであり、反り量Bは同積層板の中央部から
切り出した330×330mmの試料片の中央部の浮き上
り量を測定したものである。
尚、上記の例では、湿潤処理を施した基材だけ
で積層板を構成したが、これを一部に用いて他の
基材と組合せた積層板についても効果があつた。
第1表に示す如く本発明の方法で得られたプリ
プレグは、耳部のカール現象がなく且樹脂量のバ
ラツキが少なくなり、第2表に示す如く積層板の
反りの絶対値及び端部と中央部の反りのバラツキ
が少なくまた電気特性のバラツキ幅も小さい品質
の安定性に優れた積層板を製造できる点その工業
的価値は極めて大なるものである。[Table] The measured values in Table 2 are shown as the maximum and minimum values of the measured values of 20 samples, respectively. The amount of warpage A is
330 cut from the corner of a 1000 x 1000 mm laminate
The amount of bulge in the center of a 330mm x 330mm sample piece was measured, and the amount of warp B was measured as the amount of bulge in the center of a 330 x 330mm sample piece cut from the center of the same laminate. be. In the above example, the laminate was constructed using only the base material subjected to the wet treatment, but the effect was also obtained with a laminate using this as a part and combining it with other base materials. As shown in Table 1, the prepreg obtained by the method of the present invention has no curl phenomenon at the edges and less variation in the amount of resin, and as shown in Table 2, the absolute value of warp and the edge part of the laminate Its industrial value is extremely great in that it can produce a laminate with excellent quality stability, with little variation in warpage in the center and small variation in electrical properties.
第1図は本発明の積層板製造法のプリプレグ製
造工程を示す簡略断面図、第2図は従来の積層板
製造法のプリプレグ製造工程を示す簡略断面図で
ある。
1は巻物、2は基材、3は水蒸気或は噴霧水発
生炉、4は第1含浸槽、5は第2含浸槽、6はプ
リプレグ、7,8は乾燥炉。
FIG. 1 is a simplified sectional view showing the prepreg manufacturing process of the laminate manufacturing method of the present invention, and FIG. 2 is a simplified sectional view showing the prepreg manufacturing process of the conventional laminate manufacturing method. 1 is a scroll, 2 is a base material, 3 is a steam or spray water generating furnace, 4 is a first impregnating tank, 5 is a second impregnating tank, 6 is a prepreg, and 7 and 8 are drying furnaces.
Claims (1)
に予め湿潤処理を行い該基材中の含有水分を3〜
10重量%にした後熱硬化性樹脂を含浸乾燥して得
たプリプレグを一部乃至全部として積層成形する
ことを特徴とする積層板の製造法。1. A glass nonwoven fabric or a glass-paper mixed nonwoven fabric base material is pre-wetted to reduce the moisture content in the base material to 3 to 30%.
1. A method for manufacturing a laminate, characterized in that part or all of the prepreg obtained by impregnating and drying a thermosetting resin to 10% by weight is laminated and molded.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58198863A JPS6090757A (en) | 1983-10-24 | 1983-10-24 | Manufacture of laminated board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58198863A JPS6090757A (en) | 1983-10-24 | 1983-10-24 | Manufacture of laminated board |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6090757A JPS6090757A (en) | 1985-05-21 |
JPS6225506B2 true JPS6225506B2 (en) | 1987-06-03 |
Family
ID=16398170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58198863A Granted JPS6090757A (en) | 1983-10-24 | 1983-10-24 | Manufacture of laminated board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6090757A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2352249B (en) * | 1999-07-21 | 2004-04-14 | Rover Group | A method of manufacture of a glass fibre pre-preg for use in a polymer glazing application |
JP2008031222A (en) * | 2006-07-26 | 2008-02-14 | Matsushita Electric Works Ltd | Prepreg, production method thereof and printed wiring board |
-
1983
- 1983-10-24 JP JP58198863A patent/JPS6090757A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6090757A (en) | 1985-05-21 |
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