JPS60177033A - Production of laminated board - Google Patents

Production of laminated board

Info

Publication number
JPS60177033A
JPS60177033A JP3193284A JP3193284A JPS60177033A JP S60177033 A JPS60177033 A JP S60177033A JP 3193284 A JP3193284 A JP 3193284A JP 3193284 A JP3193284 A JP 3193284A JP S60177033 A JPS60177033 A JP S60177033A
Authority
JP
Japan
Prior art keywords
resin
base material
triamine
laminated board
phenolic resin
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
Application number
JP3193284A
Other languages
Japanese (ja)
Inventor
Takahiro Yamaguchi
貴寛 山口
Masayuki Noda
雅之 野田
Kiyoshi Osaka
喜義 大坂
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Resonac Corp
Original Assignee
Shin Kobe Electric Machinery Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shin Kobe Electric Machinery Co Ltd filed Critical Shin Kobe Electric Machinery Co Ltd
Priority to JP3193284A priority Critical patent/JPS60177033A/en
Publication of JPS60177033A publication Critical patent/JPS60177033A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To improve the moisture resistance, electrical insulating property, punchability and productivity of a laminated board, by using a small amount of a phenolic resin precondensate containing a small amount of a diamine or triamine as a resin for treating a base material in producing the laminated board of the phenolic resin on paper base material. CONSTITUTION:A triamine, e.g. ethylenediamine, or triamine, e.g. diethylene triamine, in an amount of 0.1-1wt% based on the resin solid is added to a phenolic resin precondensate, and the resultant mixture is used as a resin for treating a base material (primer resin) to treat a paper base material, which is then impregnated with a facing phenolic resin to give prepreg. Sheets of the resultant prepreg in a given number are laminated and hot-pressed to afford the amined laminated board.

Description

【発明の詳細な説明】 本発明は、基材処理用樹脂(下塗り用樹脂)として処理
効果が大きいフェノール樹脂初期縮合物を使用した生産
性の良好な紙基材フェノール樹脂積層板の製造法に関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a paper-based phenolic resin laminate with good productivity using a phenolic resin initial condensate having a large processing effect as a base material treatment resin (undercoat resin). .

ツーノール樹脂は、周知の如く、フェノールとホルマリ
ンを反応釜において所定の反応度まで反応を進行させた
後、使用しているが、一般に反応時間が5〜8時間と長
く、反応時間の短縮が望まれる。また、基材処理用樹脂
は低分子量分が多い#1ど基材への含浸性が良好となり
、基材の処理効果は大である。しかし、この場合、樹脂
の反応度は小さく、これを基材に含浸乾燥したプリプレ
グの状態で充分反応を進めるためには、乾燥時間を長く
する必要があり、塗工、乾燥。工程の生産性が大巾に低
下するという欠点がある〇 本発明は上記欠点を解決するもので、基材処理用樹脂と
して、反応度の小さいフェノール樹脂初期縮合物にジア
ミンもしくはトリアミンを該樹脂鴇形に対し0.1〜1
重量係添加したものを使用するものである。これで紙基
材を処理し、更にフェノール樹脂を含浸乾燥したプリプ
レグを積層成形するものである。
As is well known, thunol resin is used after allowing the reaction of phenol and formalin to proceed to a predetermined degree of reaction in a reaction vessel, but the reaction time is generally long at 5 to 8 hours, and it is desirable to shorten the reaction time. It will be done. In addition, the resin for substrate treatment has good impregnating properties into substrates such as #1, which have a large amount of low molecular weight, and the treatment effect of the substrate is large. However, in this case, the degree of reactivity of the resin is low, and in order to sufficiently proceed with the reaction in the prepreg state in which the resin is impregnated into the base material and dried, it is necessary to increase the drying time, which requires a long drying time. There is a drawback that the productivity of the process is greatly reduced. The present invention solves the above-mentioned drawback. As a base material treatment resin, a diamine or triamine is added to the initial condensate of a phenol resin with a low reactivity. 0.1 to 1 for the shape
The weight ratio is added. The paper base material is treated with this, and the prepreg, which has been impregnated with phenol resin and dried, is laminated and molded.

ツーノール樹脂の反応度を小さくするこ゛とにより、反
応釜との反応時間を短縮することができ、かつ低分子量
分が多くなるため、基材の処理効果が良好となり、得ら
れる積層板の耐湿性、電気絶縁性、打抜加工性を向上す
ることができる。更に、ジアミンもしくはトリアミンの
添加により、フェノール樹脂の硬化が促進されるため、
塗工、乾燥工程の生産性を低下させない。
By reducing the degree of reactivity of the Tuonol resin, the reaction time with the reaction pot can be shortened, and since the low molecular weight content is increased, the treatment effect of the base material is improved, and the moisture resistance of the resulting laminate is improved. Electrical insulation and punching workability can be improved. Furthermore, the addition of diamines or triamines accelerates the curing of phenolic resins,
Does not reduce productivity in coating and drying processes.

本発明に使用されるジアミンもしくはトリアミンは、エ
チレンジアミン、トリエチレンジアミン、ジエチレント
リアミン等特に限定しないが、未反応分がプリプレグの
乾燥中に揮散するように乾燥温度付近の沸点を有するも
のが望ましい。その添加量に関し鋭意、実験を行なった
結果、基材処理用樹脂の樹脂固形に対して0.1@量係
未満では硬化促進の効果があまり見られず、また1重量
%以上では硬化速度はほぼ飽和状態となり、添加の効果
があられれない。図面に、ノニル基変性フェノール樹脂
におけるエチレンジアミンの硬化促進効果を一例として
示した。
The diamine or triamine used in the present invention is not particularly limited, such as ethylenediamine, triethylenediamine, diethylenetriamine, etc., but it is desirable that the diamine or triamine has a boiling point near the drying temperature so that unreacted components are volatilized during drying of the prepreg. As a result of intensive experiments regarding the amount of addition, we found that if the amount is less than 0.1% by weight based on the resin solids of the base material treatment resin, there is not much effect of accelerating curing, and if it is more than 1% by weight, the curing speed is It becomes almost saturated and the effect of addition cannot be achieved. The drawing shows an example of the curing accelerating effect of ethylenediamine on a nonyl group-modified phenol resin.

また、フェノール樹脂初期縮合物は、フェノールに対し
てやや過剰のホルムアルデヒドを加え、アルカリ性触媒
により、加熱反応させたもので、分子中に多数のメチロ
ール基(−OH,OH)を保持しているものである。
In addition, the phenol resin initial condensate is obtained by adding a slight excess of formaldehyde to phenol and causing a heating reaction with an alkaline catalyst, and it has a large number of methylol groups (-OH, OH) in the molecule. It is.

更に紙基材には、クラフト紙、す/ター紙等あるが、特
に限定しない。
Further, paper base materials include kraft paper, star/tar paper, etc., but are not particularly limited.

次に、本発明の詳細な説明するっ 実施例1 リンク−紙を、ノニル基変性フェノール樹脂(ゲル化時
間8分)100重量部に対してエチレンジアミンj)、
577j量部を添加した基材処理用樹脂で処理し、含浸
乾燥後の樹脂含有量を20係とした。続いて、上塗り用
フェノール樹脂を含浸乾燥して総樹脂量50%のプリプ
レグを得た。
Next, the present invention will be described in detail. Example 1 Link paper was mixed with ethylenediamine (j),
It was treated with a substrate treatment resin containing 577 parts by weight, and the resin content after impregnation and drying was 20 parts. Subsequently, a phenolic resin for top coating was impregnated and dried to obtain a prepreg with a total resin content of 50%.

上n[Fプリプレグを所定枚数積重ね、170C−12
0kg /cr/lで30分間加熱加圧成形して1.6
fl厚の積層板を得た。
Top n[F prepreg stacked in specified number, 170C-12
1.6 by heating and pressure molding at 0kg/cr/l for 30 minutes
A laminated plate having a fl thickness was obtained.

従来例1 基材処理用樹脂として、エチレンジアミンを添加しない
ものを用いた以外は実施例1と同様にして1.6.厚の
積層板を得た。
Conventional Example 1 1.6. was carried out in the same manner as in Example 1 except that a resin to which ethylenediamine was not added was used as the base material treatment resin. A thick laminate was obtained.

従来例2 基材処理用樹脂として、ゲル化時間3分のエチレンジア
ミンを添加しないノニル基変性フェノール樹脂を用いた
以外は実施例1と同様にして1.6喘厚の積層板を得だ
Conventional Example 2 A laminate with a thickness of 1.6 was obtained in the same manner as in Example 1, except that a nonyl group-modified phenol resin without addition of ethylenediamine with a gelation time of 3 minutes was used as the base material treatment resin.

なお、ノニル基変性フェノール樹脂は、ノニルフェノー
ル1モルに対しパラホルムアルデヒド(パラホルム86
%)1.sモル、ベンジルジメチルアミン0.3モルを
加え80cで90分反応サすタ後、フェノール7モル、
パラホルムアルデヒド(ハラホルム86%)4モルを加
え80Cで所定のゲル化時間になるまで反応を進め、メ
タノールで希釈した固形分50%のものを使用した。ま
た、上塗り用のフェノール樹脂はレゾール型桐油変性フ
ェノール樹脂を使用した。噴に、ゲル化時間は、固形分
50%の樹脂0.5mlを採取し、150Cの熱盤上で
測定した。
In addition, the nonyl group-modified phenol resin contains paraformaldehyde (paraform 86
%)1. After adding 0.3 moles of benzyldimethylamine and allowing the reaction to proceed at 80°C for 90 minutes, 7 moles of phenol,
4 moles of paraformaldehyde (halaform 86%) was added and the reaction was allowed to proceed at 80C until a predetermined gelation time was reached, and a solution with a solid content of 50% diluted with methanol was used. In addition, a resol type tung oil modified phenolic resin was used as the top coating phenolic resin. The gelation time was measured by taking 0.5 ml of resin with a solid content of 50% and placing it on a hot plate at 150C.

本発明の実施例、従来例で得た積層板について、J l
5−0−6481により特性試験を行なった結果を、反
応及び塗工、乾燥工程での生産性と合せて第1表に示す
Regarding the laminates obtained in the examples of the present invention and the conventional examples, J l
Table 1 shows the results of the characteristic tests conducted according to No. 5-0-6481, together with the productivity in the reaction, coating, and drying steps.

第 1 表 第1表から明らかなように、本発明によって得られたN
t層板は、電気抵抗の吸湿劣化が小さく、吸水率が小さ
いことから、電気絶縁性及び耐浸性においC極めて優れ
ており、かつ従来例に比べて大巾に生産性が改善され、
その工業的価値は甚大である。
Table 1 As is clear from Table 1, the N obtained by the present invention
The T-layer board has low moisture absorption deterioration of electrical resistance and low water absorption, so it has extremely excellent electrical insulation and immersion resistance, and has greatly improved productivity compared to conventional products.
Its industrial value is enormous.

【図面の簡単な説明】[Brief explanation of drawings]

図面はノニル基変性フェノール樹脂におけるエチレンジ
アミンの硬化促進効果を示す曲線図である。 特許出願人 新神戸電機株式会社
The drawing is a curve diagram showing the curing accelerating effect of ethylenediamine on nonyl group-modified phenolic resin. Patent applicant Shin-Kobe Electric Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 紙基材ツーノール樹脂積層板の製造法において、基材処
理用樹脂(下塗り用樹脂)として、フェノール樹脂初期
縮合物にジアミンもしくはトリアミンを前記樹脂固形に
対し0.1−1重量係添加したものを使用することを特
徴とする積層板の製造法。
In the method for producing a paper-based two-nor resin laminate, a phenolic resin initial condensate with diamine or triamine added in a weight ratio of 0.1-1 to the solid resin is used as the base material treatment resin (undercoating resin). A method for producing a laminate, characterized in that it is used.
JP3193284A 1984-02-21 1984-02-21 Production of laminated board Pending JPS60177033A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3193284A JPS60177033A (en) 1984-02-21 1984-02-21 Production of laminated board

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3193284A JPS60177033A (en) 1984-02-21 1984-02-21 Production of laminated board

Publications (1)

Publication Number Publication Date
JPS60177033A true JPS60177033A (en) 1985-09-11

Family

ID=12344741

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3193284A Pending JPS60177033A (en) 1984-02-21 1984-02-21 Production of laminated board

Country Status (1)

Country Link
JP (1) JPS60177033A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS512872A (en) * 1974-06-26 1976-01-10 Brother Ind Ltd KAITENDENTAT SUSOCHI
JPS5198791A (en) * 1975-02-27 1976-08-31 GANSHINYOFUENOORUJUSHISOSEIBUTSUNO SEIZOHOHO
JPS57157743A (en) * 1981-03-24 1982-09-29 Shin Kobe Electric Machinery Manufacture of laminated board

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS512872A (en) * 1974-06-26 1976-01-10 Brother Ind Ltd KAITENDENTAT SUSOCHI
JPS5198791A (en) * 1975-02-27 1976-08-31 GANSHINYOFUENOORUJUSHISOSEIBUTSUNO SEIZOHOHO
JPS57157743A (en) * 1981-03-24 1982-09-29 Shin Kobe Electric Machinery Manufacture of laminated board

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