JPS628312B2 - - Google Patents
Info
- Publication number
- JPS628312B2 JPS628312B2 JP58203176A JP20317683A JPS628312B2 JP S628312 B2 JPS628312 B2 JP S628312B2 JP 58203176 A JP58203176 A JP 58203176A JP 20317683 A JP20317683 A JP 20317683A JP S628312 B2 JPS628312 B2 JP S628312B2
- Authority
- JP
- Japan
- Prior art keywords
- laminate
- prepreg
- resin
- free phenol
- base material
- 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
Landscapes
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
〔技術分野〕
この発明は、積層板の製造技術、なかんずくフ
エノール樹脂積層板の製造技術の分野に属する。
〔背景技術〕
民生用、積層板の重要特性に、打抜加工性があ
る。低温打抜加工、高密度打抜加工という、業界
のニーズから積層板樹脂は、ますます可塑化の方
向にある。
従つて、低温打抜加工用のフエノール積層板に
おけるフエノール樹脂は、ガラス転移点を低く、
おさえている。また、フリーフエノールは、可塑
化効果をもつことと、除去が困難であることか
ら、積層板中に1.0%程度ふくまれていた。ま
た、レジンペーパー(プリプレグ)中には、2.0
%程度のフリーフエノールが、ふくまれていた。
この様に、十分可塑化された低温打抜加工用積
層板は、基板としてやわらかすぎる面があつた。
また熱時における強度が、弱いという問題点もあ
つた。
〔発明の目的〕
本発明は、上記問題点である積層板の基板とし
ての強度を、低温打抜加工性を維持しつつ改良す
ることを目的とし、特に熱時の強度向上、すなわ
ち、樹脂の強度向上を目的とする。
〔発明の開示〕
通常フエノール樹脂積層板の製造方法は、フエ
ノール樹脂ワニスを、紙基材(限定する主旨では
ない)に含浸させ、加熱乾燥後、加熱加圧成形す
る。本発明は、積層板におけるフリーフエノール
濃度を減ずるために、フエノール樹脂を含浸させ
たプリプレグを加熱乾燥する工程において、減圧
することである。
従来、樹脂の基材への含浸を良くするために、
含浸工程で、減圧を試みたことはあるが、乾燥工
程ではない。なぜなら、積層中1%程度のフリー
フエノールは、可塑化効果はあつても、害はない
と判断されていたからである。
減圧のレベルは、限定されるものではないが、
−500mmHg〜−750mmHg程度が良く、減圧が大き
い程好都合である。
上記方法により、プリプレグにおけるフリーフ
エノールの含有量を、1.0%以下とするのであ
る。
上記プリプレグを用いることにより、積層板中
のフリーフエノールの含有量を、0.3%以下とす
ると一層良い結果が得られる。なお、プリプレグ
のフリーフエノール含有量を1.0%以下とすると
大低の場合積層板中では0.3以下となる。
〔発明の効果〕
以上の様にして、フリーフエノールを減じた積
層板樹脂と、減じなかつた製層板樹脂との粘弾性
スペクトルは第1図に示すようになる。これから
わかる様に、フリーフエノールを減じた樹脂は、
ヤング率が向上していることがわかる。特に、熱
時にその効果が大きい。しかし、ガラス転移点に
は差がない。さらに積層板の低温打抜加工性も、
差がない。
以下、実施例及び比較例により説明する。
実施例 1
桐油変性したフエノール樹脂を、メタノール溶
媒にて、希釈してワニスとなす。厚さ10ミルスの
クラフト紙を、ワニスに、浸漬含浸する。直ち
に、−700mmHg下、150℃〜160℃に設定下で乾燥
させる。このようにして得た樹脂含浸紙(プリプ
レグ)のフリーフエノール含有量を、ガス・クロ
マトグラフで測定したところ0.7%であつた。
このプリプレグを常法により積層成形すること
により、厚さ1.6mmの積層板を得た。積層板中に
おけるフリーフエノールを、プリプレグ同様に測
定したところ、0.1%であつた。
実施例 2
実施例1と同様であるが、減圧のレベルを−
600mmHgとした。
フリーフエノールはプリプレグ中に0.9%、積
層板中に0.3%であつた。
比較例 1
実施例1と同様であるが、樹脂含浸紙の乾燥
は、常圧下で行つた。フリーフエノールはプリプ
レグ中、2.0%、積層板中、1.0%であつた。
以上の実施例及び比較例で得た積層板の打抜加
工性と、積層板樹脂の粘弾性スペクトルを、計測
したところ、下記表に示すとおりである。
【表】DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention belongs to the field of manufacturing technology for laminates, and in particular, technology for manufacturing phenolic resin laminates. [Background technology] An important characteristic of laminates for consumer use is punching workability. Due to the industry's needs for low-temperature punching and high-density punching, laminate resins are increasingly becoming plasticized. Therefore, the phenolic resin in the phenolic laminate for low-temperature punching has a low glass transition point,
I'm holding it down. In addition, free phenol was included in the laminate in an amount of about 1.0% because it has a plasticizing effect and is difficult to remove. In addition, resin paper (prepreg) contains 2.0
% of free phenol was included. As described above, the sufficiently plasticized laminate for low-temperature punching had some aspects that were too soft as a substrate.
Another problem was that the strength was weak when heated. [Object of the Invention] The present invention aims to improve the strength of a laminate as a substrate, which is the problem described above, while maintaining low-temperature punching workability. The purpose is to improve strength. [Disclosure of the Invention] Generally, a method for producing a phenolic resin laminate is to impregnate a paper base material (not limited to this) with a phenolic resin varnish, heat and dry it, and then heat and pressure mold it. The present invention is to reduce the pressure in the process of heating and drying the prepreg impregnated with phenolic resin in order to reduce the free phenol concentration in the laminate. Conventionally, in order to improve the impregnation of resin into the base material,
I have tried reducing the pressure during the impregnation process, but not during the drying process. This is because it has been determined that about 1% of free phenol in the laminated layer is not harmful, although it may have a plasticizing effect. The level of decompression is, but is not limited to,
-500 mmHg to -750 mmHg is good, and the greater the reduced pressure, the more convenient it is. By the above method, the free phenol content in the prepreg is reduced to 1.0% or less. By using the above prepreg, better results can be obtained if the free phenol content in the laminate is set to 0.3% or less. Note that if the free phenol content of the prepreg is 1.0% or less, it will be 0.3 or less in the laminate in the case of large or low. [Effects of the Invention] As described above, the viscoelastic spectra of the laminate resin with reduced free phenol and the laminate resin with no reduction are as shown in FIG. As you can see, the resin with reduced free phenol is
It can be seen that the Young's modulus has improved. The effect is especially great when it's hot. However, there is no difference in glass transition temperature. Furthermore, the low-temperature punching processability of the laminate is
There is no difference. This will be explained below using Examples and Comparative Examples. Example 1 A varnish is prepared by diluting a phenolic resin modified with tung oil with a methanol solvent. Dip-impregnate 10 mils thick kraft paper in varnish. Immediately dry under −700 mmHg and set at 150°C to 160°C. The free phenol content of the resin-impregnated paper (prepreg) thus obtained was determined to be 0.7% by gas chromatography. This prepreg was laminated and molded using a conventional method to obtain a laminate with a thickness of 1.6 mm. Free phenol in the laminate was measured in the same manner as the prepreg and was found to be 0.1%. Example 2 Similar to Example 1, but with the level of vacuum reduced to -
It was set to 600mmHg. Free phenol was 0.9% in the prepreg and 0.3% in the laminate. Comparative Example 1 Same as Example 1, but the resin-impregnated paper was dried under normal pressure. Free phenol was 2.0% in the prepreg and 1.0% in the laminate. The punching workability of the laminates obtained in the above Examples and Comparative Examples and the viscoelastic spectrum of the laminate resins were measured, and the results are shown in the table below. 【table】
第1図は粘弾性スペクトルを表わすグラフであ
る。
FIG. 1 is a graph representing a viscoelastic spectrum.
Claims (1)
脂含浸基材を調整する含浸工程、樹脂含浸基材を
加熱乾燥してプリプレグを調整する乾燥工程、プ
リプレグを加熱加圧して積層板となす成形工程か
らなる積層板の製造法において、樹脂含浸基材の
乾燥を減圧下に行なうことを特徴とするフエノー
ル樹脂積層板の製法。 2 プリプレグ中に含まれるフリーフエノールの
含有量が1.0%以下となるまで乾燥することを特
徴とする特許請求の範囲第1項記載の製法。 3 積層板中のフリーフエノール含有量が0.3%
以下となるまで乾燥することを特徴とする特許請
求の範囲第1項記載の製法。[Claims] 1. An impregnation step in which a base material is impregnated with a phenolic resin varnish to prepare a resin-impregnated base material, a drying step in which a prepreg is prepared by heating and drying the resin-impregnated base material, and a lamination process in which the prepreg is heated and pressurized. 1. A method for producing a phenolic resin laminate comprising a step of forming a plate into a phenolic resin laminate, the method comprising drying a resin-impregnated base material under reduced pressure. 2. The manufacturing method according to claim 1, wherein the prepreg is dried until the content of free phenol contained in the prepreg is 1.0% or less. 3 Free phenol content in the laminate is 0.3%
The manufacturing method according to claim 1, characterized in that the method is dried until the following.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58203176A JPS6094351A (en) | 1983-10-28 | 1983-10-28 | Manufacture of phenol resin laminated board |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58203176A JPS6094351A (en) | 1983-10-28 | 1983-10-28 | Manufacture of phenol resin laminated board |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6094351A JPS6094351A (en) | 1985-05-27 |
| JPS628312B2 true JPS628312B2 (en) | 1987-02-21 |
Family
ID=16469713
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58203176A Granted JPS6094351A (en) | 1983-10-28 | 1983-10-28 | Manufacture of phenol resin laminated board |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6094351A (en) |
-
1983
- 1983-10-28 JP JP58203176A patent/JPS6094351A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6094351A (en) | 1985-05-27 |
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