JPH075769B2 - Method for manufacturing epoxy resin laminate - Google Patents
Method for manufacturing epoxy resin laminateInfo
- Publication number
- JPH075769B2 JPH075769B2 JP61189549A JP18954986A JPH075769B2 JP H075769 B2 JPH075769 B2 JP H075769B2 JP 61189549 A JP61189549 A JP 61189549A JP 18954986 A JP18954986 A JP 18954986A JP H075769 B2 JPH075769 B2 JP H075769B2
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- bisphenol
- resin laminate
- laminate
- varnish
- 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 - Lifetime
Links
Landscapes
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
- Epoxy Resins (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、耐熱性に優れ、成形性、加工性の良いエポキ
シ樹脂積層板の製造方法に関するものである。TECHNICAL FIELD The present invention relates to a method for producing an epoxy resin laminate having excellent heat resistance, moldability and workability.
近年、印刷回路板の製造工程においてはその高精度、高
密度化に併い、加工工程において、より高温にさらされ
る為、より耐熱性の優れた積層板が望まれている。In recent years, in the manufacturing process of a printed circuit board, along with its high accuracy and high density, the printed circuit board is exposed to higher temperatures in the processing step, so that a laminated board having more excellent heat resistance is desired.
従来、耐熱性エポキシ積層板の樹脂処方においてはビス
フェノールA型エポキシ樹脂に3官能性以上のエポキシ
樹脂(クレゾールノボラック型やフェノールノボラック
型)を配合することにより、耐熱性に優れた積層板を得
ていた。Conventionally, in a resin formulation of a heat-resistant epoxy laminate, a bisphenol A type epoxy resin is mixed with a trifunctional or higher-functional epoxy resin (cresol novolac type or phenol novolac type) to obtain a laminate excellent in heat resistance. It was
しかし3官能性以上のエポキシ樹脂の配合量を増加する
に伴い、耐熱性の向上(ガラス転移温度の増加など)は
得られるが、反面3官能性以上のエポキシ樹脂特有の急
速なゲル化にともなう、積層板の成形不良および加圧時
のひずみによる寸法安定性の低下が認められる。さらに
架橋点増加による、ドリル加工時のドリル刃摩耗を発生
する。However, as the compounding amount of the trifunctional or higher epoxy resin is increased, the heat resistance is improved (such as the glass transition temperature is increased), but the rapid gelation peculiar to the trifunctional or higher epoxy resin is accompanied. In addition, deterioration of dimensional stability due to defective molding of the laminated plate and strain during pressurization is observed. Furthermore, due to the increase in cross-linking points, wear of the drill blade during drilling occurs.
更に、3官能性以上のエポキシ樹脂の多量配合は高コス
トとなり望ましくない。Furthermore, blending a large amount of a trifunctional or higher epoxy resin is not desirable because it results in high cost.
〔発明の目的〕 本発明は、従来の耐熱性を低下させることなく、積層板
の成形性を向上し、ドリル加工時の問題を解消すること
を目的に研究して、本発明を完成するに至ったものであ
る。[Object of the invention] The present invention was studied for the purpose of improving the formability of a laminated plate and eliminating the problems at the time of drilling without lowering the conventional heat resistance, to complete the present invention. It has come.
本発明は、3官能性以上のエポキシ樹脂を分子量300〜1
000のビスフェノールA型エポキシ樹脂及びビスフェノ
ールA系化合物と共縮合して得られるエポキシ樹脂を主
成分とするワニスを調整し、このワニスを基材に含浸
し、得られたプリプレグを積層し、加熱、加圧成形する
ことを特徴とするエポキシ樹脂積層板の製造方法であ
る。The present invention uses a trifunctional or higher functional epoxy resin having a molecular weight of 300 to 1
A varnish whose main component is an epoxy resin obtained by co-condensing 000 bisphenol A-type epoxy resins and bisphenol A-based compounds is prepared, a base material is impregnated with this varnish, and the obtained prepreg is laminated and heated. A method for producing an epoxy resin laminate, which is characterized by performing pressure molding.
本発明において、用いられる共縮合系エポキシ樹脂は3
官能性以上のエポキシ樹脂を10〜20%の割合で共縮合し
て得られるエポキシ樹脂が好ましい。In the present invention, the co-condensed epoxy resin used is 3
An epoxy resin obtained by co-condensing an epoxy resin having a functionality of 10 to 20% is preferable.
従来、耐熱性の優れた積層板を得るには、3官能性以上
のエポキシ樹脂をビスフェノールA型エポキシ樹脂に両
者の合計に対して20〜30%配合しているが、本発明の共
縮合エポキシ樹脂を使用した場合、3官能性以上のエポ
キシ樹脂の割合を10〜20%に減少しても従来と同程度の
耐熱性を得ることができる。Conventionally, in order to obtain a laminate having excellent heat resistance, a bisphenol A type epoxy resin is blended with a bisphenol A type epoxy resin in an amount of 20 to 30% based on the total amount of the two. When a resin is used, even if the proportion of the epoxy resin having a functionality of 3 or more is reduced to 10 to 20%, it is possible to obtain the same heat resistance as the conventional one.
これは従来の3官能性以上のエポキシ樹脂を配合する場
合に比較して、共縮合の場合の方が均一に反応すること
によるものと考えられる。It is considered that this is because the reaction in the case of co-condensation is more uniform than that in the case of blending a conventional epoxy resin having three or more functional groups.
この3官能性以上のエポキシ樹脂の減少効果と均一な反
応によって、積層板成形時の成形不良を大巾に改善する
ことができ、通常行なわれる加圧よりも、低い圧力で成
形することができる。Due to the effect of reducing the epoxy resin having three or more functionalities and the uniform reaction, it is possible to greatly improve the molding failure at the time of molding the laminated plate, and it is possible to mold at a pressure lower than the normally applied pressure. .
このことは加圧時のひずみが減少することにより、寸法
安定性の向上に大きな効果が認められ、又積層板の板厚
精度も向上する。This has a great effect on the improvement of dimensional stability by reducing the strain at the time of pressurization, and also improves the plate thickness accuracy of the laminated plate.
更にドリル加工時のドリル刃摩耗も大巾に改善される。
これは3官能性以上のエポキシ樹脂の減少によるものと
考えられる。Furthermore, the wear of the drill blade during drilling is greatly improved.
It is considered that this is due to the reduction of the epoxy resin having a functionality of 3 or more.
3官能性以上のエポキシ樹脂としてはフェノールノボラ
ック型又はクレゾールノボラック型エポキシ樹脂が好ま
しく使用される。As the trifunctional or higher functional epoxy resin, a phenol novolac type epoxy resin or a cresol novolac type epoxy resin is preferably used.
本発明により得られたエポキシ樹脂積層板においては耐
熱性を低下させることなく、3官能性以上のエポキシ樹
脂を減少でき、従来より成形性に優れ、特に低圧加圧が
可能となり、寸法安定性が著しく向上する。In the epoxy resin laminate obtained according to the present invention, the epoxy resin having a functionality of 3 or more can be reduced without lowering the heat resistance, the moldability is superior to the conventional one, and particularly the low pressure can be applied, and the dimensional stability is improved. Remarkably improved.
更に、ドリル加工時のドリル刃摩耗も大巾に減少するこ
とができ、工業的なエポキシ樹脂積層板の製造方法とし
て好適である。Further, the wear of the drill blade during drilling can be greatly reduced, which is suitable as an industrial method for producing an epoxy resin laminate.
以下に本発明の実施例及び比較例を示す。 Examples and comparative examples of the present invention will be shown below.
実施例 共縮合系エポキシ樹脂の製造 撹拌機、温度計、窒素ガス導入管及び外部加熱源を備え
た、容器内に、「エピコート828」(油化シェル社製ビ
スフェノールAエポキシ樹脂:エポキシ当量190)190
部、テトラブロムビスフェノールA200部、1%苛性ソー
ダ水溶液0.2部を加え、窒素ガスをパージしながら180℃
の温度で5時間反応せしめることにより、水酸基当量が
710である予備縮合物を得た。Example Production of co-condensation type epoxy resin In a container equipped with a stirrer, a thermometer, a nitrogen gas introducing pipe and an external heating source, "Epicoat 828" (Bisphenol A epoxy resin manufactured by Yuka Shell Co .: epoxy equivalent 190) 190
Part, tetrabrom bisphenol A 200 parts, 1% caustic soda solution 0.2 parts, and nitrogen gas purging at 180 ° C
By reacting for 5 hours at the temperature of
A precondensate of 710 was obtained.
更に、同様の容器に、この予備縮合物46部、「エピコー
ト828」44部、「エピコート180S65」(油化シェル社
製、クレゾールノボラック型エポキシ樹脂:エポキシ当
量220)10部を用い、さらに1%テトラメチルアンモニ
ウムクロライド水溶液の0.28部を加え、140℃で4時間
反応せしめた後、メチルイソブチルケトン92部を加え、
溶解させることにより、エポキシ当量470で臭素化率20
%の共縮合エポキシ樹脂を得た。Further, 46 parts of this precondensate, 44 parts of "Epicoat 828" and 10 parts of "Epicoat 180S65" (made by Yuka Shell Co., cresol novolac type epoxy resin: epoxy equivalent 220) were used in the same container, and further 1% 0.28 parts of tetramethylammonium chloride aqueous solution was added, and after reacting at 140 ° C. for 4 hours, 92 parts of methyl isobutyl ketone was added,
When dissolved, the bromination rate is 20 with an epoxy equivalent of 470.
% Co-condensed epoxy resin was obtained.
エポキシ樹脂積層板の製造 エポキシ樹脂配合ワニスの組成は次の通りである。Production of Epoxy Resin Laminated Plate The composition of the epoxy resin-containing varnish is as follows.
上記配合材料を総固形分として50重量%となるようメチ
ルセロソルブ及びアセトンの溶剤で溶解しワニスを作製
した。 A varnish was prepared by dissolving the above blended materials in a solvent of methyl cellosolve and acetone so that the total solid content was 50% by weight.
このワニスをガラスクロスに含浸させ乾燥させた後、樹
脂分45%のプリプレグを得た。このプリプレグを8枚重
ね、更にその両面に18μ銅箔を1枚ずつ重ね、プレスに
て加熱、加圧成形して厚さ1.6mmのエポキシ樹脂積層板
を得た。After the glass cloth was impregnated with this varnish and dried, a prepreg having a resin content of 45% was obtained. Eight sheets of this prepreg were overlaid, and one sheet of 18 μ copper foil was overlaid on each side of the prepreg, and heated and pressed by a press to obtain an epoxy resin laminate having a thickness of 1.6 mm.
比較例 前記の樹脂配合のエポキシ樹脂を用いて実施例と同様の
方法によりエポキシ樹脂積層板を得た。Comparative example An epoxy resin laminate was obtained by using the above-mentioned resin-blended epoxy resin in the same manner as in the example.
表1に実施例と比較例で得たエポキシ樹脂積層板の評価
結果を示す。Table 1 shows the evaluation results of the epoxy resin laminates obtained in Examples and Comparative Examples.
本発明によって製造したエポキシ樹脂積層板は、成形
性、耐熱性、ドリル加工性に優れているのみならず、プ
リント回路板としての一般特性も良好であり、優れた実
用特性を有していることが確認された。 The epoxy resin laminate manufactured according to the present invention is not only excellent in moldability, heat resistance, and drill workability, but also has good general characteristics as a printed circuit board and has excellent practical characteristics. Was confirmed.
Claims (1)
〜1000のビスフェノールA型エポキシ樹脂及びビスフェ
ノールA系化合物と共縮合して得られるエポキシ樹脂を
主成分とするワニスを調製し、このワニスを基材に含浸
し、得られたプリプレグを積層し、加熱加圧成形するこ
とを特徴とするエポキシ樹脂積層板の製造方法。1. A trifunctional or higher functional epoxy resin having a molecular weight of 300.
~ 1000 bisphenol A type epoxy resin and a varnish whose main component is an epoxy resin obtained by co-condensing with a bisphenol A type compound are prepared, the varnish is impregnated into a substrate, and the obtained prepreg is laminated and heated. A method for producing an epoxy resin laminate, which comprises pressure molding.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61189549A JPH075769B2 (en) | 1986-08-14 | 1986-08-14 | Method for manufacturing epoxy resin laminate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61189549A JPH075769B2 (en) | 1986-08-14 | 1986-08-14 | Method for manufacturing epoxy resin laminate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6346234A JPS6346234A (en) | 1988-02-27 |
| JPH075769B2 true JPH075769B2 (en) | 1995-01-25 |
Family
ID=16243177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61189549A Expired - Lifetime JPH075769B2 (en) | 1986-08-14 | 1986-08-14 | Method for manufacturing epoxy resin laminate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH075769B2 (en) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5426600A (en) * | 1977-07-29 | 1979-02-28 | Sato Kusutaka | Device for attaching and detaching fluorescent lamps |
| JPS5996178A (en) * | 1982-11-22 | 1984-06-02 | Dainippon Ink & Chem Inc | Coating composition |
| JPS61148226A (en) * | 1984-12-21 | 1986-07-05 | Toto Kasei Kk | Solid epoxy resin for paint and laminated board |
| JPS61179221A (en) * | 1985-02-04 | 1986-08-11 | Toshiba Chem Corp | Epoxy glass/copper laminate |
| JPS61188413A (en) * | 1985-02-18 | 1986-08-22 | Dainippon Ink & Chem Inc | Epoxy resin composition |
-
1986
- 1986-08-14 JP JP61189549A patent/JPH075769B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6346234A (en) | 1988-02-27 |
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