JPS60127347A - Phenolic resin molding material - Google Patents
Phenolic resin molding materialInfo
- Publication number
- JPS60127347A JPS60127347A JP23560683A JP23560683A JPS60127347A JP S60127347 A JPS60127347 A JP S60127347A JP 23560683 A JP23560683 A JP 23560683A JP 23560683 A JP23560683 A JP 23560683A JP S60127347 A JPS60127347 A JP S60127347A
- Authority
- JP
- Japan
- Prior art keywords
- phenolic resin
- molding material
- resin molding
- ion concentration
- filler
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は電子機器、電気機器、コンピューター等に用因
られるフェノ−l樹脂成形材料に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a phenol resin molding material used for electronic equipment, electrical equipment, computers, etc.
最近の電子機器、電気機器、コンビニ−ター等において
は高性能化、小型化指向が強くこのため使用される合成
樹脂部品にも算囲気温度上昇に対処するだめの耐熱性向
上及び長期寿命化に対処する丸めの耐電蝕性向上、耐加
水分解性向上げ要望されていた。従来よく使用されて−
る一般用フエノール樹脂成形材料は耐熱性、耐加水分解
性に優れるが耐電蝕性が劣り、ポリブチレンテレフタレ
ート成形材料は耐電蝕性に優れるが耐熱性、耐加水分解
性が劣り、ポリプロピレン成形材料は耐電蝕性、耐加水
分解性に優れるが耐熱性に劣る等−長一短があり全てに
満足する成形材料はなかった。Recent electronic equipment, electric equipment, convenience stores, etc. are highly oriented toward higher performance and smaller size.As a result, the synthetic resin parts used are required to have improved heat resistance and longer service life to cope with the rise in ambient air temperature. There were requests for improvements in the electrical corrosion resistance and hydrolysis resistance of the rounded parts. Traditionally commonly used
General-purpose phenolic resin molding materials have excellent heat resistance and hydrolysis resistance, but poor galvanic corrosion resistance, polybutylene terephthalate molding materials have excellent galvanic corrosion resistance, but poor heat resistance and hydrolysis resistance, and polypropylene molding materials have It has advantages and disadvantages, such as excellent galvanic corrosion resistance and hydrolysis resistance, but poor heat resistance, and there has been no molding material that satisfies all of them.
本発明は上記要望に応えるため耐電蝕性、耐熱性、耐加
水分解性に優れたフェノール樹脂成形材料を提供するこ
とにある。The object of the present invention is to provide a phenolic resin molding material having excellent electrolytic corrosion resistance, heat resistance, and hydrolysis resistance in order to meet the above-mentioned needs.
本発明は塩素イオン濃度10ppm 以下のフェノ−A
/樹脂に、塩素イオン成度20ppmJg下の充填剤を
添加してなることを特徴とするフェノ−y@脂成形材料
で以下本発明の詳細な説明する。The present invention provides pheno-A with a chloride ion concentration of 10 ppm or less.
The present invention will be described in detail below using a pheno-y@fat molding material, which is characterized in that it is made by adding a filler having a chloride ion content of 20 ppmJg or less to a resin.
本発明に用いるフェノール樹脂は塩素イオン渋皮10p
pm以下であるならばノボラック型フェノ−1v樹脂、
レゾール型フェノ−/l/ @j脂の何れであってもよ
く更に単独、混合物、変性物であってもよ込ものである
。ただノボラック型フェノ−jv樹脂にあっては塩酸等
のように含塩素触媒を使用することはフェノール樹脂中
の含塩素イオン濃度が大となるので本発明では用偽られ
なh0又フェノ−M樹脂中のフリーフェノール蝋が0.
5重量係(以下単に係と記す)以下であることが耐電蝕
性、耐熱性、耐加水分解性を向上せしめる傾向があり望
ましいことである。充填剤としては塩素イオン濃度20
ppm以下の充填剤があるならばよく特に限定するもの
ではな−が好ましくは塩素イオンを除去しやすb無機充
填剤を周込ることが望ましhことである。又、充填剤量
は特に限定するものではないが好ましくは全量の50〜
80俤であることが耐熱性、成形性のバランスを保つ上
で望ましいことである。上記フェノ−iv樹脂、充填剤
以外の添加剤としてはフェノール樹脂成形材料に一般に
用いられている離型剤、着色剤、必要に応じて硬化剤を
添加、混練、粉砕し更に必要に応じて造粒してフェノ−
1v樹脂成形材料とするものである。The phenolic resin used in the present invention is chloride ion astringent skin 10p
If it is below pm, novolac type pheno-1v resin,
It may be any of the resol type phenol/l/@j fats, and may be used singly, as a mixture, or as a modified product. However, in the case of novolak type pheno-JV resin, the use of a chlorine-containing catalyst such as hydrochloric acid increases the concentration of chlorine-containing ions in the phenol resin, so it cannot be used in the present invention for h0 or pheno-M resin. Free phenol wax inside is 0.
It is desirable that the weight ratio be 5 or less (hereinafter simply referred to as "weight ratio") as this tends to improve electrolytic corrosion resistance, heat resistance, and hydrolysis resistance. As a filler, the chloride ion concentration is 20
There is no particular limitation as long as there is a filler of ppm or less, but it is preferable to include an inorganic filler that facilitates the removal of chlorine ions. The amount of filler is not particularly limited, but is preferably 50 to 50% of the total amount.
A thickness of 80 yen is desirable in order to maintain a balance between heat resistance and moldability. Additives other than the above pheno-IV resin and filler include mold release agents and coloring agents that are commonly used in phenolic resin molding materials, as well as curing agents as needed, kneaded, and pulverized. Grain and pheno-
1v resin molding material.
以下本発明を実施例にもとずbて説明する。The present invention will be explained below based on examples.
フェノール1モルに対しホpムアlレデヒド0.85モ
ルを37チホルマリンで加え蓚酸触媒で還流温度下60
分間反応させて塩素イオン濃度7ppm(2)ノボラッ
ク型フェノ−tV@脂を得た。次に該°フェノール樹脂
34重量部(以下単に部と記す)に対し塩素イオン濃度
15ppmの炭酸カルシウム0部、へキサミツ4部、ス
テアリン酸1部、カーボンブラック1部を加え混線、粉
砕し、てフェノール樹脂成形材料を得た。To 1 mole of phenol, 0.85 mole of hopal redehyde was added with 37% formalin, and the mixture was heated at reflux temperature at 60% using an oxalic acid catalyst.
The reaction was carried out for a minute to obtain a novolak type pheno-tV@fat with a chloride ion concentration of 7 ppm (2). Next, 0 parts of calcium carbonate with a chloride ion concentration of 15 ppm, 4 parts of hexamic acid, 1 part of stearic acid, and 1 part of carbon black were added to 34 parts by weight of the phenol resin (hereinafter simply referred to as "parts"), mixed, and pulverized. A phenolic resin molding material was obtained.
〔比較例1〕
蓚酸触媒を塩酸触媒として反応させた以外は実施例と同
様に処理して塩素イオン旋J:i80ppmのフェノ−
/I/樹脂を得、該フェノ−7し樹脂を用−た以外は実
施例と同様に処理してフェノ−/I/樹脂成形材料を得
た。[Comparative Example 1] The same procedure as in Example was carried out except that the oxalic acid catalyst was used as a hydrochloric acid catalyst.
A Pheno/I/ resin molding material was obtained by processing in the same manner as in Example except that the Pheno-7 resin was used.
〔比較例2〕
実施例と同じフェノ−M樹脂を用b、炭酸カlレシウム
の代りに塩素イオン濃度260ppmのガラス繊維粉末
を用いた以外は実施例と同様に処理してフェノール樹脂
成形材料を得た。[Comparative Example 2] A phenol resin molding material was prepared in the same manner as in the example except that the same pheno-M resin as in the example was used and glass fiber powder with a chloride ion concentration of 260 ppm was used instead of calcium carbonate. Obtained.
〔比較例3〕
炭酸カルシウムの代りに塩素イオン濃度1600の木粉
を用いた以外は実施例と同様に処理してフェノール樹脂
成形材料を得た。[Comparative Example 3] A phenol resin molding material was obtained in the same manner as in Example except that wood flour with a chloride ion concentration of 1600 was used instead of calcium carbonate.
〔比較例4〕
炭酸力々ンウムの代りに塩素イオン濃度200のパルプ
を用いた以外は実施例と同様に処理してフェノール樹脂
成形材料を得た。[Comparative Example 4] A phenolic resin molding material was obtained in the same manner as in the example except that pulp with a chloride ion concentration of 200 was used instead of carbonate.
実施例と比較例1乃至4のフェノール樹脂成形材料をコ
ンデンサーキャップ用金型にて成形圧力100’q/c
4.150℃で3分間成形シテ成形品ヲ得、該成形品の
耐電蝕性、耐熱性、耐加水分解性を評価した結果は第1
表で明白なように本発明のフェノール樹脂成形材料から
得られた成形品の性能はよく本発明の優れていることを
確認した。The phenolic resin molding materials of Examples and Comparative Examples 1 to 4 were molded at a molding pressure of 100'q/c in a condenser cap mold.
4. A molded product was obtained by molding at 150℃ for 3 minutes, and the results of evaluating the electrolytic corrosion resistance, heat resistance, and hydrolysis resistance of the molded product were the first.
As is clear from the table, the performance of molded articles obtained from the phenolic resin molding material of the present invention was well confirmed to be superior to that of the present invention.
第 1 表 特許出願人 松下電工株式会社 代理人弁理士 竹元敏丸(ほか2名)Table 1 patent applicant Matsushita Electric Works Co., Ltd. Representative Patent Attorney Toshimaru Takemoto (and 2 others)
Claims (2)
に、塩素イオン濃度20ppmAJ、下の充填剤を添加
してなることを特徴とするフェノ−V樹脂成形材料。(1) A pheno-V resin molding material characterized by being made by adding a filler with a chloride ion concentration of 20 ppm AJ or less to a phenol resin with a chloride ion concentration of 10 ppm or less.
ことを特徴とする特許請求の範囲第1項記載のフェノ−
/I/樹脂成形材料。(2) The phenol according to claim 1, characterized in that the amount of the filler is from % to % by weight of the total amount.
/I/Resin molding material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23560683A JPS60127347A (en) | 1983-12-13 | 1983-12-13 | Phenolic resin molding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23560683A JPS60127347A (en) | 1983-12-13 | 1983-12-13 | Phenolic resin molding material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60127347A true JPS60127347A (en) | 1985-07-08 |
Family
ID=16988496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23560683A Pending JPS60127347A (en) | 1983-12-13 | 1983-12-13 | Phenolic resin molding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60127347A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61113641A (en) * | 1984-11-09 | 1986-05-31 | Sumitomo Bakelite Co Ltd | Phenolic resin composition for electrolytic corrosion resistance use |
JPS61296051A (en) * | 1985-06-24 | 1986-12-26 | Sumitomo Bakelite Co Ltd | Phenolic resin composition resistant to electrolytic corrosion |
-
1983
- 1983-12-13 JP JP23560683A patent/JPS60127347A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61113641A (en) * | 1984-11-09 | 1986-05-31 | Sumitomo Bakelite Co Ltd | Phenolic resin composition for electrolytic corrosion resistance use |
JPH0223576B2 (en) * | 1984-11-09 | 1990-05-24 | Sumitomo Bakelite Co | |
JPS61296051A (en) * | 1985-06-24 | 1986-12-26 | Sumitomo Bakelite Co Ltd | Phenolic resin composition resistant to electrolytic corrosion |
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