JPH05162129A - Manufacture of prepreg - Google Patents
Manufacture of prepregInfo
- Publication number
- JPH05162129A JPH05162129A JP33097591A JP33097591A JPH05162129A JP H05162129 A JPH05162129 A JP H05162129A JP 33097591 A JP33097591 A JP 33097591A JP 33097591 A JP33097591 A JP 33097591A JP H05162129 A JPH05162129 A JP H05162129A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- prepreg
- base material
- impregnated
- polyimide
- 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 abstract description 7
- 238000001035 drying Methods 0.000 claims abstract description 8
- 239000011261 inert gas Substances 0.000 claims abstract description 4
- 238000010926 purge Methods 0.000 claims 1
- 239000011347 resin Substances 0.000 abstract description 23
- 229920005989 resin Polymers 0.000 abstract description 23
- 239000000463 material Substances 0.000 abstract description 10
- 238000005187 foaming Methods 0.000 abstract description 7
- -1 polyethylene terephthalate Polymers 0.000 abstract description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000835 fiber Substances 0.000 abstract description 4
- 229920001721 polyimide Polymers 0.000 abstract description 4
- 239000003822 epoxy resin Substances 0.000 abstract description 3
- 239000011521 glass Substances 0.000 abstract description 3
- 229920000647 polyepoxide Polymers 0.000 abstract description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 3
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 3
- 229920000742 Cotton Polymers 0.000 abstract description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004642 Polyimide Substances 0.000 abstract description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 abstract description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 2
- 239000000919 ceramic Substances 0.000 abstract description 2
- 239000004927 clay Substances 0.000 abstract description 2
- 229910052570 clay Inorganic materials 0.000 abstract description 2
- 239000000945 filler Substances 0.000 abstract description 2
- 239000012784 inorganic fiber Substances 0.000 abstract description 2
- 239000004745 nonwoven fabric Substances 0.000 abstract description 2
- 239000005011 phenolic resin Substances 0.000 abstract description 2
- 229920006122 polyamide resin Polymers 0.000 abstract description 2
- 239000009719 polyimide resin Substances 0.000 abstract description 2
- 239000000843 powder Substances 0.000 abstract description 2
- 239000000377 silicon dioxide Substances 0.000 abstract description 2
- 239000000454 talc Substances 0.000 abstract description 2
- 229910052623 talc Inorganic materials 0.000 abstract description 2
- 229920006337 unsaturated polyester resin Polymers 0.000 abstract description 2
- 239000002759 woven fabric Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract 1
- 238000005470 impregnation Methods 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920006380 polyphenylene oxide Polymers 0.000 description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、電子機器、電気機器、
コンビュ−タ−、通信機器等に用いられる積層板用プリ
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 electronic equipment, electric equipment,
The present invention relates to a method for manufacturing a prepreg for laminated plates used in computers, communication devices and the like.
【0002】[0002]
【従来の技術】従来、プリプレグは樹脂中の有機溶剤、
モノマーによる爆発を避けるため、熱風乾燥機、輻射熱
乾燥機で、風力を多くして乾燥していた。従って風速を
3m/秒以上にして乾燥させているが、熱風乾燥機にあ
っては空気伝熱のため樹脂含浸基材表面から昇温し発泡
状態になり表面凹凸となり、内部発泡の多いプリプレグ
になる。又輻射熱乾燥機にあっては熱風乾燥機より改善
されるが、それでも未だ満足できる状態ではない。更に
共通の欠点として溶剤上昇速度が早くなり、益々発泡し
やすくなる問題があった。2. Description of the Related Art Conventionally, prepreg is an organic solvent in resin,
In order to avoid the explosion caused by the monomer, it was dried by using a hot air dryer or a radiant heat dryer to increase the wind power. Therefore, it is dried at a wind speed of 3 m / sec or more, but in a hot air dryer, the heat transfer from the air causes the temperature to rise from the surface of the resin-impregnated base material into a foamed state, resulting in surface irregularities, resulting in a prepreg with a lot of internal foaming. Become. Also, the radiant heat dryer can be improved as compared with the hot air dryer, but it is still not in a satisfactory state. Further, as a common drawback, there is a problem that the solvent rising speed becomes faster and foaming is more likely to occur.
【0003】[0003]
【発明が解決しようとする課題】従来の技術で述べたよ
うに、従来の樹脂含浸基材の乾燥には問題があった。本
発明は従来の技術における上述の問題点に鑑みてなされ
たもので、その目的とするところは表面凹凸がなく、内
部発泡のないプリプレグの製造方法を提供することにあ
る。As described in the prior art, there is a problem in drying the conventional resin-impregnated base material. The present invention has been made in view of the above problems in the prior art, and an object of the present invention is to provide a method for producing a prepreg having no surface irregularities and no internal foaming.
【0004】[0004]
【課題を解決するための手段】本発明は、樹脂を含浸し
た基材を、乾燥風速0.2〜2m/秒にて乾燥し、必要
に応じて不活性ガスでパージすることを特徴とするプリ
プレグの製造方法のため、上記目的を達成することがで
きたもので、以下本発明を詳細に説明する。The present invention is characterized in that a base material impregnated with a resin is dried at a drying air velocity of 0.2 to 2 m / sec and, if necessary, purged with an inert gas. The above object can be achieved because of the method of manufacturing a prepreg, and the present invention will be described in detail below.
【0005】本発明に用いる樹脂含浸基材の樹脂は、フ
ェノ−ル樹脂、エポキシ樹脂、不飽和ポリエステル樹
脂、ポリイミド樹脂、ポリアミド樹脂、ポリエチレンテ
レフタレート樹脂、ポリブチレンテレフタレート樹脂、
ポリフェニレンサルファイド樹脂、ポリフェニレンオキ
サイド樹脂、フッソ樹脂、ポリブタジエン樹脂等の単
独、変性物、混合物樹脂に、必要に応じてタルク、クレ
ー、シリカ、炭酸カルシュウム、水酸化アルミニゥム等
の無機質粉末充填剤を添加したものである。基材として
はガラス、セラミック、アスベスト等の無機質繊維や、
ビニルアルコ−ル、ポリイミド、ポリエチレンテレフタ
レート、ポリブチレンテレフタレート、ポリアミド、ポ
リフエニレンサルフアイド、ポリフエニレンオキサイ
ド、フッ素樹脂等の有機質繊維や木綿等の天然繊維から
なる織布、不織布、紙等である。基材に含浸させる樹脂
量は樹脂固形分として35〜70重量%が好ましい。更
に樹脂は同一の樹脂のみによる含浸でもよいが、同系樹
脂又は異系樹脂により1次含浸、2次含浸というように
含浸を複数にし、より含浸が均一になるようにしてもよ
い。乾燥機は熱風乾燥機、輻射熱乾燥機等のように乾燥
機全般を用いることができるが、乾燥風速を0.2〜2
m/秒にして乾燥することが必要である。即ち0.2m
/秒未満では乾燥性が低下し、2m/秒をこえると表面
凹凸、内部発泡がなくならないためである。又安全上、
必要に応じて窒素ガス等の不活性ガスでパージするもの
である。更に乾燥機の形式は、縦型、横型等何れでもよ
いが、好ましくは縦型を用いることが望ましい。以下本
発明を実施例に基づいて説明する。The resin of the resin-impregnated base material used in the present invention includes phenol resin, epoxy resin, unsaturated polyester resin, polyimide resin, polyamide resin, polyethylene terephthalate resin, polybutylene terephthalate resin,
Polyphenylene sulfide resin, polyphenylene oxide resin, fluorine resin, polybutadiene resin, etc., alone, modified, or mixed resin, with inorganic powder filler such as talc, clay, silica, calcium carbonate, aluminum hydroxide added as necessary. Is. As the base material, inorganic fibers such as glass, ceramics and asbestos,
Examples thereof include vinyl alcohol, polyimide, polyethylene terephthalate, polybutylene terephthalate, polyamide, polyphenylene sulfide, polyphenylene oxide, woven fabrics, non-woven fabrics and papers made of organic fibers such as fluororesin and natural fibers such as cotton. The amount of resin with which the substrate is impregnated is preferably 35 to 70% by weight as a resin solid content. Further, the resin may be impregnated only with the same resin, but may be made into a plurality of impregnations such as primary impregnation and secondary impregnation with the same resin or different type resin so that the impregnation becomes more uniform. As the dryer, a general dryer such as a hot air dryer or a radiant heat dryer can be used, but the drying wind speed is 0.2 to 2
It is necessary to dry at m / sec. That is 0.2 m
This is because if it is less than / sec, the drying property is deteriorated, and if it exceeds 2 m / sec, surface irregularities and internal foaming are not eliminated. For safety,
If necessary, it is purged with an inert gas such as nitrogen gas. Further, the dryer may be of any type such as vertical type or horizontal type, but it is preferable to use the vertical type. The present invention will be described below based on examples.
【0006】[0006]
【実施例】厚み0.2mmのガラス織布に、硬化剤含有
エポキシ樹脂を乾燥後樹脂量が45重量%になるように
含浸した樹脂含浸基材を縦型輻射熱乾燥機に送り、乾燥
風力を0.8m/秒にして乾燥しプリプレグを得た。[Example] A resin-impregnated base material, in which a hardener-containing epoxy resin was dried on a glass woven cloth having a thickness of 0.2 mm so that the amount of the resin was 45% by weight, was sent to a vertical radiant heat dryer, and dry wind was applied. It was dried at 0.8 m / sec to obtain a prepreg.
【0007】[0007]
【比較例】乾燥風力を3m/秒にした以外は実施例と同
様に処理してプリプレグを得た。[Comparative Example] A prepreg was obtained by treating in the same manner as in Example except that the dry wind power was changed to 3 m / sec.
【0008】実施例及び比較例のプリプレグの性能は表
1のようである。Table 1 shows the performance of the prepregs of Examples and Comparative Examples.
【0009】[0009]
【表1】 [Table 1]
【0010】[0010]
【発明の効果】本発明は上述したごとく構成されてい
る。特許請求の範囲に記載した構成を有するプリプレグ
の製造方法においては、表面凹凸、内部発泡が無く、本
発明の優れていることを確認した。The present invention is constructed as described above. In the method for producing a prepreg having the structure described in the claims, it was confirmed that the present invention was excellent because there were no surface irregularities or internal foaming.
Claims (1)
〜2m/秒にて乾燥し、必要に応じて不活性ガスでパー
ジすることを特徴とするプリプレグの製造方法。1. A dry air velocity of 0.2
A method for producing a prepreg, which comprises drying at ˜2 m / sec and purging with an inert gas as necessary.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33097591A JPH05162129A (en) | 1991-12-16 | 1991-12-16 | Manufacture of prepreg |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33097591A JPH05162129A (en) | 1991-12-16 | 1991-12-16 | Manufacture of prepreg |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH05162129A true JPH05162129A (en) | 1993-06-29 |
Family
ID=18238442
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP33097591A Pending JPH05162129A (en) | 1991-12-16 | 1991-12-16 | Manufacture of prepreg |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH05162129A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010048122A1 (en) * | 2008-10-22 | 2010-04-29 | Cytec Technology Corp. | Improved processing of polymer matrix composites |
-
1991
- 1991-12-16 JP JP33097591A patent/JPH05162129A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010048122A1 (en) * | 2008-10-22 | 2010-04-29 | Cytec Technology Corp. | Improved processing of polymer matrix composites |
| JP2012506480A (en) * | 2008-10-22 | 2012-03-15 | サイテク・テクノロジー・コーポレーシヨン | Improved processing of polymer matrix composites |
| AU2009307761B2 (en) * | 2008-10-22 | 2014-10-23 | Cytec Technology Corp. | Improved processing of polymer matrix composites |
| US9186851B2 (en) | 2008-10-22 | 2015-11-17 | Cytec Technology Corp. | Processing of polymer matrix composites |
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