JPH0360861B2 - - Google Patents
Info
- Publication number
- JPH0360861B2 JPH0360861B2 JP4364687A JP4364687A JPH0360861B2 JP H0360861 B2 JPH0360861 B2 JP H0360861B2 JP 4364687 A JP4364687 A JP 4364687A JP 4364687 A JP4364687 A JP 4364687A JP H0360861 B2 JPH0360861 B2 JP H0360861B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- resol type
- varnish
- prepreg
- 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.)
- Expired
Links
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 22
- 239000002966 varnish Substances 0.000 claims description 21
- 229920003987 resole Polymers 0.000 claims description 14
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims description 12
- 229930003836 cresol Natural products 0.000 claims description 12
- 239000005011 phenolic resin Substances 0.000 claims description 10
- 239000011248 coating agent Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 5
- 229920002678 cellulose Polymers 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 5
- 238000005470 impregnation Methods 0.000 claims description 5
- 229920001568 phenolic resin Polymers 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000011134 resol-type phenolic resin Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 2
- 238000000465 moulding Methods 0.000 claims description 2
- 238000003825 pressing Methods 0.000 claims 1
- 239000002904 solvent Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002655 kraft paper Substances 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 229940100630 metacresol Drugs 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
Description
産業上の利用分野
本発明は、フエノール樹脂系積層板の製造法に
関する。
従来の技術
積層板の製造工程において、基材に樹脂ワニス
を含浸塗工する工程は最も重要なものである。含
浸の良否が積層板の性能、特に沿層耐電圧を左右
し、また、塗工速度が積層板製造の作業能率に大
きく影響する。
含浸性を良くするためには、
樹脂ワニスの粘度を下げる。
基材の樹脂ワニスへの浸漬時間を長くする。
樹脂ワニスの親水性を増し、基材を構成する
セルロースへの親水性を上げる。
基材を脱泡処理する。
物理的な手段(ロールで押し込む等)を施
す。
などの手段が考えられる。
従来、採用されているのは、の方法、具体的
には、ワニスの溶剤分を多くしたり、ワニス温度
を上げることであり、また、の方法、具体的に
は、基材のワニスへの浸漬距離を長くしたり、塗
工速度を下げる方法である。このように、基材に
樹脂ワニスを含浸塗工後乾燥してプリプレグを
得、このプリプレグを積層成形して積層板が製造
される。
発明が解決しようとする問題点
従来採用されている方法のうち、溶剤分を多く
することは、乾燥工程で揮散する溶剤のガス濃度
が高くなり、安全面、衛生面で好ましくないばか
りか、コスト的にも不利である。ワニス温度を上
げる方法は、ワニスを変質させるので、ワニスを
使用できる時間を短くし制限される。また、浸漬
距離を長くする方法は、設備が大きくなり、塗工
速度を下げる方法は、作業能率を低下させるので
好ましくない。
本発明は、上記の点に鑑み、の点に着目して
フエノール樹脂系の積層板の製造において、特性
の優れた積層板を、安全な環境で能率よく製造で
きるようにすることを目的とする。
問題点を解決するための手段
上記目的を達成するために、本発明は、レゾー
ル型クレゾール樹脂に水溶性低分子量レゾール型
フエノール樹脂を混合した混合ワニスをセルロー
ス基材に含浸塗工する点に特徴を有する。含浸塗
工後乾燥して得たプリプレグを所要枚数重ね、こ
れを加熱加圧成形して積層板とするものである。
作 用
本発明では、一般に油溶性であるレゾール型ク
レゾール樹脂に、これと相溶性があり、かつ水溶
性の低分子量レゾール型フエノール樹脂を混合し
ている。この低分子量レゾール型フエノール樹脂
の存在により、セルロース基材との親和性が高く
なり、特に溶剤分を多くすることなく樹脂ワニス
の基材への含浸性を良くするものである。
実施例
本発明に使用するレゾール型クレゾール樹脂の
原料となるクレゾールは、メタクレゾールとパラ
クレゾールの混合物が一般的であるが、その一部
をフエノールに置きかえたものであつてもよい。
水溶性低分子量レゾール型フエノール樹脂の原料
は、フエノールが一般的であるが、アルキルフエ
ノールを混合しても差しつかえない。
水溶性低分子量レゾール型フエノール樹脂のレ
ゾール型クレゾール樹脂への混合割合は、十分な
含浸性を確保するために5〜20重量%が好まし
い。20重量%を越える場合は、加熱加圧成形した
とき樹脂の硬度が上がり、積層板の加工性が悪く
なる点で望ましくない。また、混合ワニスをセル
ロース基材に含浸塗工するとき、30〜50℃に加温
しておくとワニス粘度を下げることができ、含浸
性が一層良くなるので、更に使用する溶剤量を減
らすことができる。尚、50℃を越えて加温する
と、溶剤の揮散が激しくなり、かえつて好ましく
ない。
実施例 1
メタクレゾール100重量部に37%ホルマリン90
重量部、25%アンモニア水4重量部を反応釜に投
入し、100℃で60分間反応させる。その後減圧濃
縮を行い反応生成物の所定ゲルタイムで反応を終
了し、メタノールで所定粘度まで希釈しレゾール
型クレゾール樹脂を得た。一方、フエノール60重
量部37%ホルマリン100重量部、トリメチルアミ
ン6重量部を反応釜に投入し、75℃で3時間反応
後減圧濃縮を行い反応生成物の所定ゲルタイムで
反応を終了し、メタノールで所定粘度まで希釈し
水溶性低分子量レゾール型フエノール樹脂を得
た。
上記ワニスを固型分重量比でレゾール型クレゾ
ール樹脂/水溶性低分子量レゾール型フエノール
樹脂=10/1で混合し、この混合ワニスを温度35
℃、粘度100cpsで坪量135g/m2のクラフト紙に
15秒含浸させ、その後20m/分の速度で乾燥を行
い、樹脂量51%、樹脂フロー5%のプリプレグを
得た。このプリプレグを80枚積み重ね、160℃−
100Kg/m2で45分間加熱し、厚さ15〓の積層板を
得た。
比較例 1
実施例と同じレゾール型クレゾール樹脂のみを
使用して、他は実施例1と全く同じ条件で製造
し、厚さ15mmの積層板を得た。
従来例 1
実施例1と同じレゾール型クレゾール樹脂のみ
を使用し、ワニス温度20℃、粘度30cpsで坪量135
g/m2のクラフト紙に25秒含浸させ、その後12
m/分の速度で乾燥を行い樹脂量51%、樹脂フロ
ー5%のプリプレグを得た。このプリプレグを使
用し、実施例1と同じ条件で厚さ15mmの積層板を
得た。
従来例 2
実施例と同じレゾール型クレゾール樹脂のみを
使用し、ワニス温度20℃、粘度30cpsで坪量135
g/m2のクラフト紙に15秒含浸させ、20m/分の
速度で乾燥を行い、従来例1と同じ特性のプリプ
レグを得た。このプリプレグを使用し、実施例1
と同じ条件で厚さ15mmの積層板を得た。
上記で得た各積層板の特性を第1表に示す。
INDUSTRIAL APPLICATION FIELD The present invention relates to a method for manufacturing a phenolic resin-based laminate. Prior Art In the manufacturing process of laminates, the most important step is to impregnate and coat the base material with resin varnish. The quality of impregnation affects the performance of the laminate, especially the along-line withstand voltage, and the coating speed greatly affects the efficiency of manufacturing the laminate. To improve impregnation, lower the viscosity of the resin varnish. Increase the time the substrate is immersed in the resin varnish. Increases the hydrophilicity of the resin varnish and increases the hydrophilicity of the cellulose that makes up the base material. Defoaming the base material. Apply physical means (such as pushing with a roll). Possible methods include: Conventionally, methods used include increasing the solvent content of the varnish or raising the varnish temperature; This method involves increasing the immersion distance or lowering the coating speed. In this way, a prepreg is obtained by impregnating and coating a base material with a resin varnish and drying it, and the prepreg is laminated and molded to produce a laminate. Problems to be Solved by the Invention Among conventional methods, increasing the solvent content increases the gas concentration of the solvent that evaporates during the drying process, which is not only undesirable from a safety and hygiene perspective, but also increases cost. It is also disadvantageous. The method of increasing the varnish temperature alters the quality of the varnish, thus shortening and limiting the time during which the varnish can be used. Further, the method of increasing the immersion distance requires larger equipment, and the method of lowering the coating speed is undesirable because it reduces work efficiency. In view of the above points, an object of the present invention is to enable efficient production of laminates with excellent properties in a safe environment in the production of phenolic resin-based laminates. . Means for Solving the Problems In order to achieve the above object, the present invention is characterized in that a cellulose base material is impregnated and coated with a mixed varnish in which a water-soluble low molecular weight resol type phenol resin is mixed with a resol type cresol resin. has. A required number of prepregs obtained by impregnation coating and drying are stacked together, and then heated and pressed to form a laminate. Function In the present invention, a resol type cresol resin, which is generally oil-soluble, is mixed with a low molecular weight resol type phenolic resin which is compatible with the cresol resin and is water-soluble. The presence of this low molecular weight resol type phenolic resin increases the affinity with the cellulose base material and improves the impregnation of the resin varnish into the base material without particularly increasing the solvent content. Examples Cresol used as a raw material for the resol-type cresol resin used in the present invention is generally a mixture of meta-cresol and para-cresol, but it may also be one in which a part of the mixture is replaced with phenol.
The raw material for water-soluble low molecular weight resol type phenolic resin is generally phenol, but alkylphenol may also be mixed therein. The mixing ratio of the water-soluble low molecular weight resol type phenol resin to the resol type cresol resin is preferably 5 to 20% by weight in order to ensure sufficient impregnability. If it exceeds 20% by weight, it is undesirable because the hardness of the resin increases when hot and pressure molded, resulting in poor workability of the laminate. In addition, when impregnating and coating a cellulose base material with a mixed varnish, heating the varnish to 30 to 50°C will lower the viscosity of the varnish and improve its impregnating properties, making it possible to further reduce the amount of solvent used. I can do it. It should be noted that heating above 50°C is even more undesirable because the solvent volatilizes more vigorously. Example 1 37% formalin 90 in 100 parts by weight of metacresol
Add 4 parts by weight of 25% aqueous ammonia into a reaction vessel, and react at 100°C for 60 minutes. Thereafter, the reaction was concentrated under reduced pressure to complete the reaction at a predetermined gel time of the reaction product, and diluted with methanol to a predetermined viscosity to obtain a resol type cresol resin. On the other hand, 60 parts by weight of phenol, 100 parts by weight of 37% formalin, and 6 parts by weight of trimethylamine were charged into a reaction vessel, and after reacting at 75°C for 3 hours, the reaction was concentrated under reduced pressure. A water-soluble low molecular weight resol type phenol resin was obtained by diluting it to a viscosity. The above varnish is mixed at a solid weight ratio of resol type cresol resin/water-soluble low molecular weight resol type phenol resin = 10/1, and this mixed varnish is heated to 35
℃, viscosity 100cps, basis weight 135g/ m2 kraft paper
It was impregnated for 15 seconds and then dried at a speed of 20 m/min to obtain a prepreg with a resin content of 51% and a resin flow of 5%. 80 sheets of this prepreg were stacked at 160℃−
Heated at 100Kg/ m2 for 45 minutes to obtain a 15mm thick laminate. Comparative Example 1 A laminate with a thickness of 15 mm was obtained using only the same resol type cresol resin as in the example and otherwise under the same conditions as in the example 1. Conventional example 1 Using only the same resol type cresol resin as in Example 1, varnish temperature 20℃, viscosity 30cps, basis weight 135
g/ m2 kraft paper for 25 seconds, then 12
Drying was carried out at a speed of m/min to obtain a prepreg with a resin content of 51% and a resin flow of 5%. Using this prepreg, a laminate with a thickness of 15 mm was obtained under the same conditions as in Example 1. Conventional Example 2 Using only the same resol type cresol resin as in the example, the varnish temperature was 20℃, the viscosity was 30cps, and the basis weight was 135.
A prepreg having the same properties as Conventional Example 1 was obtained by impregnating kraft paper at a concentration of g/m 2 for 15 seconds and drying at a speed of 20 m/min. Using this prepreg, Example 1
A laminate with a thickness of 15 mm was obtained under the same conditions. Table 1 shows the characteristics of each laminate obtained above.
【表】
発明の効果
本発明によれば、その実施例と比較例および従
来例との比較から明らかなように、溶剤使用量を
抑さえて高い粘度で、また速い速度で塗工を行な
いながら、従来の低粘度、低速塗工で得られたプ
リプレグを加熱加圧成形した積層板と特性上遜色
ない優れた積層板を製造することができる。溶剤
の使用量を少なくして安全面、衛生面で問題な
く、また能率よく特性の優れた積層板を製造でき
る点、その工業的価値は極めて大である。[Table] Effects of the Invention According to the present invention, as is clear from the comparison between the examples, comparative examples, and conventional examples, it is possible to suppress the amount of solvent used, achieve high viscosity, and perform coating at high speed. , it is possible to produce an excellent laminate that is comparable in properties to a laminate made by heating and press-molding a prepreg obtained by conventional low-viscosity, low-speed coating. Its industrial value is extremely great in that it can efficiently produce laminates with excellent properties without any safety or hygiene problems by using less solvent.
Claims (1)
レゾール型フエノール樹脂を混合し、該混合ワニ
スをセルロース基材に含浸塗工し加熱乾燥してプ
リプレグを得、このプリプレグの所要枚数を重
ね、加熱加圧成形することを特徴とするフエノー
ル樹脂系積層板の製造法。 2 水溶性低分子量レゾール型フエノール樹脂の
混合比率が5〜20重量%である特許請求の範囲第
1項記載のフエノール樹脂系積層板の製造法。 3 含浸塗工時の混合ワニスの温度が30〜50℃で
ある特許請求の範囲第1項記載のフエノール樹脂
系積層板の製造法。[Claims] 1. A resol type cresol resin is mixed with a water-soluble low molecular weight resol type phenol resin, the mixed varnish is impregnated and coated on a cellulose base material, and the prepreg is obtained by heating and drying, and the required number of sheets of this prepreg is determined. A method for producing a phenolic resin-based laminate, which is characterized by stacking and heat-pressing molding. 2. The method for producing a phenolic resin laminate according to claim 1, wherein the mixing ratio of the water-soluble low molecular weight resol type phenolic resin is 5 to 20% by weight. 3. The method for producing a phenolic resin laminate according to claim 1, wherein the temperature of the mixed varnish during impregnation coating is 30 to 50°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4364687A JPS63210141A (en) | 1987-02-26 | 1987-02-26 | Production of phenol resin laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4364687A JPS63210141A (en) | 1987-02-26 | 1987-02-26 | Production of phenol resin laminate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63210141A JPS63210141A (en) | 1988-08-31 |
JPH0360861B2 true JPH0360861B2 (en) | 1991-09-18 |
Family
ID=12669627
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4364687A Granted JPS63210141A (en) | 1987-02-26 | 1987-02-26 | Production of phenol resin laminate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63210141A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5207499B2 (en) * | 2007-03-30 | 2013-06-12 | スターライト工業株式会社 | Phenol resin composite and method for producing the same |
-
1987
- 1987-02-26 JP JP4364687A patent/JPS63210141A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS63210141A (en) | 1988-08-31 |
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