JPS6028434A - Preparation of laminate - Google Patents
Preparation of laminateInfo
- Publication number
- JPS6028434A JPS6028434A JP13617083A JP13617083A JPS6028434A JP S6028434 A JPS6028434 A JP S6028434A JP 13617083 A JP13617083 A JP 13617083A JP 13617083 A JP13617083 A JP 13617083A JP S6028434 A JPS6028434 A JP S6028434A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- water
- base material
- impregnated
- drying
- 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.)
- Granted
Links
Landscapes
- Laminated Bodies (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、耐湿性、電気絶縁性か優れしかも安価に得ら
れる積層板の製造法1こ関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a laminate that has excellent moisture resistance and electrical insulation properties and can be obtained at low cost.
セルロース繊維混抄のガラス不織布基材は、ガラス繊維
単独の不織布に比べ安価に得られ、しかも機械的強度が
大きい。しかし、セルロース繊維混抄ガラス不繊布基材
1こ通常のエポキシ樹脂の如き疎水性樹脂を直接食浸し
、乾燥後、これを積層成形した場合、得られた積層板の
耐湿性、電気絶縁性が悪いという欠点を有していた。A glass nonwoven fabric base material mixed with cellulose fibers can be obtained at a lower cost than a nonwoven fabric made only of glass fibers, and has greater mechanical strength. However, when a hydrophobic resin such as an ordinary epoxy resin is directly eroded into a cellulose fiber-mixed glass nonwoven base material, and this is then laminated and molded after drying, the resulting laminate has poor moisture resistance and electrical insulation. It had the following drawback.
本発明は、上記欠点を解決するもので、アルコキシ基と
エポキシ基またはアミノ基とを併せ有するシラン化合物
を添加した水溶性エポキシ樹脂の水溶液または有機溶剤
溶液を、予めセルロース繊維混抄ガラス不織布基材に含
浸乾燥した後、該含浸基材にエポキシ樹脂を含浸、乾燥
して得たプリプレグを積層成形するものである。The present invention solves the above-mentioned drawbacks by applying an aqueous solution or an organic solvent solution of a water-soluble epoxy resin containing a silane compound having both an alkoxy group and an epoxy group or an amino group to a glass nonwoven fabric base material mixed with cellulose fibers in advance. After impregnation and drying, the prepreg obtained by impregnating the impregnated base material with an epoxy resin and drying is laminated and molded.
前記シラン化合物に含まれるアルコキシ基(S 1−0
R)は、加水分解されてシラノール基(3i−OH)と
なり、基材のガラス繊維表面と結合する。一方、アミノ
基またはエポキシ基は、後工程で含浸するエポキシ樹脂
および前記基材処理用の水溶性エポキシ樹脂と相溶して
結合し、更に、水溶性エポキシ樹脂は、セルロース繊維
混抄ガラス不繊布基材中に含まれるセルロース繊維の内
部まで浸透し、そのエポキシ基が後工程で含浸するエポ
キシ樹脂と反応し、セルロース繊維混抄がラス不織布基
材とエポキシ樹脂の緊密性を増して耐湿性、電気絶縁性
を向上させる。すなわち、セルロース繊維混抄が不
う1布基材を使用したエポキシ樹脂積層板は、前記シラ
ン化合物および水溶性エポキシ樹脂を併用すること;こ
よって初めて積層板の耐湿性、電気絶縁性を向上するこ
とができる。The alkoxy group (S 1-0
R) is hydrolyzed to become a silanol group (3i-OH), which is bonded to the glass fiber surface of the base material. On the other hand, the amino group or epoxy group is compatible with and bonded to the epoxy resin to be impregnated in the subsequent process and the water-soluble epoxy resin for treating the base material, and furthermore, the water-soluble epoxy resin is bonded to the cellulose fiber-mixed glass nonwoven fabric base. It penetrates into the inside of the cellulose fibers contained in the material, and the epoxy group reacts with the epoxy resin impregnated in the subsequent process, and the cellulose fiber mixed paper increases the tightness between the lath nonwoven fabric base material and the epoxy resin, resulting in moisture resistance and electrical insulation. Improve your sexuality. That is, for an epoxy resin laminate using a fabric base material that is not mixed with cellulose fibers, the silane compound and water-soluble epoxy resin should be used in combination; only in this way can the moisture resistance and electrical insulation of the laminate be improved. I can do it.
本発明に使用されるセルロース繊維混抄がラス不織布基
材は、クラフト、マニラ麻、みつまた等のセルロース系
パルプを一部混抄したガラス繊維を主体とする不繊布で
あり、通常の抄紙機化で抄造したものである。また、シ
ラン化合物は分子中にアルコキシ基とアミノ基またはエ
ポキシ基とを併せ有するシラン化合物で第1表に示すも
のが適当である。The cellulose fiber-mixed lath nonwoven fabric base material used in the present invention is a nonwoven fabric mainly made of glass fibers partially mixed with cellulose pulp such as kraft, manila hemp, and mitsumata, and is made using a normal paper machine. It is something. Suitable silane compounds include those shown in Table 1 having both an alkoxy group and an amino group or an epoxy group in the molecule.
水溶性エポキシ樹脂は、エチレングリコールシフリシジ
ルエーテル、トリエチレンクリコールジグリシジルエー
テル、グリセリンジグリシジルエーテル等のポリエーテ
ル結合を持つジェポキシ化合物か゛適当であり、酸、ア
ミン類等のエポキシ樹脂用硬化剤、酸性もしくは塩基性
の硬化促進剤を添加し、水溶液または有機溶剤溶液とし
て使用する。なお、水溶性エポキシ樹脂の含浸付着量は
、乾燥後の重量で5〜20重量%か゛適当である。The water-soluble epoxy resin is suitably a jepoxy compound having a polyether bond such as ethylene glycol diglycidyl ether, triethylene glycol diglycidyl ether, or glycerin diglycidyl ether, and a curing agent for epoxy resin such as acid or amine. , an acidic or basic curing accelerator is added and used as an aqueous solution or an organic solvent solution. Note that the amount of water-soluble epoxy resin that is impregnated and deposited is suitably 5 to 20% by weight after drying.
第 1 表 次に本発明の実施例について述べる。Table 1 Next, embodiments of the present invention will be described.
実施例 重量比で(ガラス/マニラg)=oo/l。Example In weight ratio (glass/manila g) = oo/l.
の混抄紙基材に水溶性エポキシ樹脂を付着量が12重i
sとなるよう含浸し乾燥した。水溶性エポキシ樹脂は、
シ」ラダイン80MF(商品名、共栄社油脂化学工業■
製)50重量部に、ジシアンジアミド(DrCY)2重
量部、ベンジルジメチルアミン(BDMA)03重量部
、シラン化合物(KBM−403)1重量を添加配合し
たものである。The amount of water-soluble epoxy resin applied to the mixed paper base material is 12 layers.
s and dried. Water-soluble epoxy resin is
Radyne 80MF (product name, Kyoeisha Yushi Kagaku Kogyo)
2 parts by weight of dicyandiamide (DrCY), 03 parts by weight of benzyldimethylamine (BDMA), and 1 part by weight of a silane compound (KBM-403) were added to 50 parts by weight of (manufactured by).
次lこ、上記含浸基材にエポキシ樹脂を総付着ff16
0重量%となるよう含浸し乾燥してプリプレグを得た。Next, apply epoxy resin to the above impregnated base materialff16
It was impregnated to a concentration of 0% by weight and dried to obtain a prepreg.
このエポキシ樹脂は、エポン1045 (商品名、浦化
シェルエポキシ■製)100重量部にDICY4重量部
、BDMAo、5重量部を添加配合したものである。This epoxy resin was prepared by adding 4 parts by weight of DICY and 5 parts by weight of BDMAo to 100 parts by weight of Epon 1045 (trade name, manufactured by Uraka Shell Epoxy ■).
上記プリプレグを積層し、温度1.70℃。The above prepregs were laminated at a temperature of 1.70°C.
圧力80#/cmで30分間加熱加圧成形した。Heat and pressure molding was carried out at a pressure of 80#/cm for 30 minutes.
従来例
実施例と同様の基材に水溶性エポキシ樹脂を含浸せず、
直接実施例と同様のエポキシ樹脂を含浸、乾燥してプリ
プレグを得、これを実施例と同条件で加熱加圧成形した
。Conventional example The same base material as in the example was not impregnated with water-soluble epoxy resin,
A prepreg was obtained by directly impregnating the same epoxy resin as in the example and drying, which was then molded under heat and pressure under the same conditions as in the example.
実施例、従来例で得た積層板の特性をJIS−C−64
81に準拠して測定した結果を第2表に示す。The characteristics of the laminates obtained in the examples and conventional examples were determined according to JIS-C-64.
Table 2 shows the results measured in accordance with 81.
第 2 表
第2表かられかるよう奢こ、本発明1こよって得られた
積層板は、従来のもの1こ比べ吸湿による電気抵抗の劣
化か小さく、吸水率が小さいことから電気絶縁性及び耐
湿性において極めて優れたものである点、その工業的価
値は甚大である。Table 2 As can be seen from Table 2, the laminate obtained according to the present invention 1 has less deterioration in electrical resistance due to moisture absorption than the conventional one, and has low water absorption, so it has excellent electrical insulation and Its industrial value is enormous because it has extremely excellent moisture resistance.
特許出願人patent applicant
Claims (1)
るシラン化合物を添加した水溶性エポキシ樹脂をセルロ
ース繊維混抄がラス不織布基材に含浸乾燥し5次いで該
含浸基材にエポキシ樹脂を含浸乾燥して得たプリプレグ
を積層成形することを特徴とする積層板の製造法。A water-soluble epoxy resin to which a silane compound having both an alkoxy group and an epoxy group or an amino group was added was impregnated into a lath nonwoven fabric base material using a cellulose fiber mixture and dried, and then the impregnated base material was impregnated with the epoxy resin and dried. A method for manufacturing a laminate, characterized by laminating and molding prepreg.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13617083A JPS6028434A (en) | 1983-07-26 | 1983-07-26 | Preparation of laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13617083A JPS6028434A (en) | 1983-07-26 | 1983-07-26 | Preparation of laminate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6028434A true JPS6028434A (en) | 1985-02-13 |
JPH0129375B2 JPH0129375B2 (en) | 1989-06-09 |
Family
ID=15168956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13617083A Granted JPS6028434A (en) | 1983-07-26 | 1983-07-26 | Preparation of laminate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6028434A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61296199A (en) * | 1985-06-20 | 1986-12-26 | 山陽国策パルプ株式会社 | Raw paper form electric insulating laminate board |
JPH02127593A (en) * | 1988-11-07 | 1990-05-16 | Sanyo Kokusaku Pulp Co Ltd | Laminate base paper and production thereof |
JP2005054326A (en) * | 2003-08-06 | 2005-03-03 | Doshisha | Method for producing natural fiber-reinforced polymeric composite material |
JP2011246592A (en) * | 2010-05-26 | 2011-12-08 | Panasonic Electric Works Co Ltd | Molding material and molding |
-
1983
- 1983-07-26 JP JP13617083A patent/JPS6028434A/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61296199A (en) * | 1985-06-20 | 1986-12-26 | 山陽国策パルプ株式会社 | Raw paper form electric insulating laminate board |
JPH02127593A (en) * | 1988-11-07 | 1990-05-16 | Sanyo Kokusaku Pulp Co Ltd | Laminate base paper and production thereof |
JPH0447079B2 (en) * | 1988-11-07 | 1992-07-31 | Sanyo Kokusaku Pulp Co | |
JP2005054326A (en) * | 2003-08-06 | 2005-03-03 | Doshisha | Method for producing natural fiber-reinforced polymeric composite material |
JP2011246592A (en) * | 2010-05-26 | 2011-12-08 | Panasonic Electric Works Co Ltd | Molding material and molding |
Also Published As
Publication number | Publication date |
---|---|
JPH0129375B2 (en) | 1989-06-09 |
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