JPS58142932A - Preparation of phenolic resin molding material - Google Patents
Preparation of phenolic resin molding materialInfo
- Publication number
- JPS58142932A JPS58142932A JP2644782A JP2644782A JPS58142932A JP S58142932 A JPS58142932 A JP S58142932A JP 2644782 A JP2644782 A JP 2644782A JP 2644782 A JP2644782 A JP 2644782A JP S58142932 A JPS58142932 A JP S58142932A
- Authority
- JP
- Japan
- Prior art keywords
- molding material
- phenolic resin
- resin molding
- glass fiber
- pulverized
- 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.)
- Granted
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
この妬明社、機械的強度にすぐれたフェノール樹脂成形
材料を得る丸めの7エノール樹脂成形材料の製法に関す
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a rounded 7-enol resin molding material that provides a phenolic resin molding material with excellent mechanical strength.
自動車の一ン電テータ、クラッチ中ブレーキまわ参に、
近時、フェノール樹脂の使用されることが多くなった。For use in automobiles when turning the energizer, clutch, or brake.
Recently, phenolic resins have been increasingly used.
このような部分に使用されるフェノール樹脂成形材料と
しては、高温時の回転性など高温時の機械的強度にすぐ
れていることが要求される。Phenolic resin molding materials used in such parts are required to have excellent mechanical strength at high temperatures, such as rotatability at high temperatures.
そζで、従来は、充填材としてアスベストヲ採用し1配
の要望を横えずようにしていたのであるが、アスベスト
の害が指摘されるなどが原因して、これに代わ夛得る充
填材が求められるようになってき*、 ガラス繊維がそ
のような代替品として極めて有望であると考えられえ。Therefore, in the past, asbestos was used as a filling material to avoid meeting the first demand, but as the harmful effects of asbestos were pointed out, alternative filling materials were used. *Glass fiber is considered to be extremely promising as such a substitute.
しかし、実際に使用してみると、予IBK反して必要な
機械的強度の得られな%fh仁とが分かつえ。However, when it is actually used, it becomes clear that, contrary to the IBK, the necessary mechanical strength cannot be obtained.
この発明は、このような事情に鑑みなされた−のであっ
て、充填材の少なくとも一部としてガラス繊維を用い・
、えとえば−げ強さで15にシーm1以上、シャルピー
衝撃強さで7 kg−cm/cm”以上というよりな高
強度を持つフェノール樹脂成形材料をつくり得るフェノ
ール樹脂成形材料の製法を提供することを目的とする。This invention was made in view of these circumstances, and it uses glass fiber as at least a part of the filler.
To provide a method for producing a phenolic resin molding material, which can produce a phenolic resin molding material having higher strength, for example, 15 cm/cm or more in burr strength and 7 kg-cm/cm" or more in Charpy impact strength. The purpose is to
発明者の研究、II察したところによると、ガラス繊維
を用いても所期の効果が得られない原因は、次のところ
にある。すなわち、フェノール樹脂成形材料の製造工1
1には混練工程や粉砕工程が必要工程として含まれるた
め、混練時や粉砕時にガラス繊維(ガラスチョップ)が
細断され、本来持っている強度が発揮されないのである
。According to the inventor's research, the reason why the desired effect cannot be obtained even when using glass fibers is as follows. That is, manufacturing process 1 of phenolic resin molding material
1 includes a kneading process and a crushing process as necessary processes, so the glass fibers (glass chops) are shredded during kneading and crushing, and their original strength is not exhibited.
そこで、フェノール樹脂成形材料の製造にあた抄、ガラ
ス繊維は粉砕工S研Kr&加するよう和した。その結果
、機械的強度にすぐれたフェノール樹脂成形材料が得ら
れえ。このようにしてこの発明が完成され友。Therefore, in order to manufacture phenolic resin molding materials, the glass fibers were processed by grinding process. As a result, a phenolic resin molding material with excellent mechanical strength can be obtained. This is how this invention was completed.
すなわち、この発明は、フェノール樹脂に成形材料とし
て必要な材料を配合しえものを混錬し、粉砕してフェノ
ール樹脂成形材料を得るにあたり、ガラス繊維を粉砕工
程11Klk添加することを4111とするフェノール
樹脂成形材料の製法をその要旨とする。以下にこれを詳
しく述べる。That is, in this invention, when a phenol resin is blended with materials necessary as a molding material, the mixture is kneaded and crushed to obtain a phenol resin molding material, glass fiber is added in the crushing step 11Klk. The gist is the manufacturing method of resin molding materials. This will be explained in detail below.
フェノール樹kF1通常のものでよく、41に限定はな
い。し九がって、その製造方法も通常のとお)である。The phenolic tree kF1 may be any ordinary one, and is not limited to 41. Therefore, the manufacturing method is also the same.
このようにして得られたフェノール樹WiIK対し、成
形材料として必要な良く知られた種々の材料を配合する
。へ中葉メチレンテトラミンなどの硬化剤やステアリン
酸塩などの添加剤あるいは着色剤などである。必要に応
じ、カラス線維以外の充填材を配合してもよい。The phenolic tree WiIK thus obtained is blended with various well-known materials necessary as a molding material. These include curing agents such as methylenetetramine, additives such as stearate, and coloring agents. If necessary, fillers other than glass fiber may be added.
得られ九配合物を通常のとおり混練し、粉砕する。1N
&練手段中験砕手段はいずれ4通常の手段による。The resulting nine formulations are kneaded and ground as usual. 1N
&The testing and crushing means during the kneading process are all 4 conventional methods.
粉砕工程後にガラス繊維の11&加が行なわれる。After the crushing step, the glass fibers are subjected to 11&addition.
添加手段は公知のとおりである。ガラス繊維としては、
集束剤の付着してい&1100〜30G#のものが好ま
しい。しかし、それに限られるものでなく、1〜3 m
alの集束し九ガラスチョツプド°ヌトランドで4良い
。しかし、ガラスチョップは集束がほぐれにくく、ガラ
スの均一分散が得にくい。The addition means are as known. As glass fiber,
It is preferable that a sizing agent is attached and the number is 1100 to 30G#. However, it is not limited to this, and 1 to 3 m
Al's focus is 9 glass chopped ° Nutland and 4 good. However, the glass chop is difficult to unfocus, and it is difficult to obtain uniform dispersion of the glass.
ガラス繊維の添加量としては、5憾を下まわると効果が
小さく、20憾を上まわると成形品の外観が悪くなる等
の問題が生じるおそれがあるので、5〜20重量参に選
ぶことが好まし込が、これに限定されるものではない。As for the amount of glass fiber added, if it is less than 5 ml, the effect will be small, and if it exceeds 20 ml, problems such as poor appearance of the molded product may occur, so it is recommended to choose between 5 and 20 ml. The preference is not limited to this.
この発明にかかるフェノール樹脂成形材料の製法によれ
ば、このようにガラス繊維を粉砕工程後にi&加するよ
う托しているため、ガラス繊維が切断、粉砕されず、本
来持っている強度を寥分に発揮する。そのため、機械的
強度の高いフェノール樹脂成形材料をつくることができ
、る。According to the manufacturing method of the phenolic resin molding material according to the present invention, since the glass fibers are subjected to I& after the pulverization process, the glass fibers are not cut or pulverized, and their original strength is significantly reduced. Demonstrate. Therefore, it is possible to create a phenolic resin molding material with high mechanical strength.
つぎに、実施例を比較例と併せて述べる。Next, examples will be described together with comparative examples.
王妃の配合物を混線、@砕したのち、第1表の添加量で
ガラス繊維を後添加(比較例は後添加なし)することに
よってフェノール11&成形材料を得た。Phenol 11 & molding material was obtained by mixing and crushing the Queen's mixture, and then post-adding glass fiber in the amount shown in Table 1 (no post-addition was made in the comparative example).
ノボラック型フェノール樹脂s2重量IG(MP 90
℃)
ヘキサメチレンテトラミン 6重量憾ステアリン
# 1重量略着 色 剤
1重量参・木 粉
4G重量参得られた各フェノール樹脂成形材料を用い
てつくった成形品について、曲げ強さ、シ、ヤルビー衝
撃強さおよび外観を調べえ結果は、第1表のとおりであ
り、実施例はいずれも比較例よりすぐれていえ。Novolac type phenolic resin s2 weight IG (MP 90
℃) Hexamethylenetetramine 6 weight Stearin # 1 weight Coloring agent
1 weight ginseng/wood powder
4G weight reference Molded products made using each of the obtained phenolic resin molding materials were examined for bending strength, shear strength, hard impact strength, and appearance.The results are shown in Table 1. It is also better than the comparative example.
!1表! 1 table
Claims (1)
を配合したものを混練し、粉砕してフェノール樹脂成形
材料を得るにあた)、ガラス繊維を粉砕工程*に後温加
することを特徴とするフェノールIIIIiI成形材料
の製法。 (り ガラス繊維として、集束剤め付着していない10
0〜300.のものが選ばれる特許請求の範囲第1項紀
軌のフェノール樹脂成形材料の製法。 (3) ガラス繊維の添加量が5〜20重量惨に選ば
れる特許請求の範S纂1項または第2項記載の7エノー
ル樹脂成形材料の製法。[Claims] (1) When phenolic resin is mixed with materials necessary as a molding material and pulverized to obtain a phenolic resin molding material), glass fibers are heated after the pulverization process*. A method for producing a phenol IIIiI molding material. (As a glass fiber, there is no sizing agent attached.)
0-300. A method for producing a phenolic resin molding material according to claim 1, in which the following is selected. (3) The method for producing a 7-enol resin molding material according to claim 1 or 2, wherein the amount of glass fiber added is selected from 5 to 20% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2644782A JPS58142932A (en) | 1982-02-19 | 1982-02-19 | Preparation of phenolic resin molding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2644782A JPS58142932A (en) | 1982-02-19 | 1982-02-19 | Preparation of phenolic resin molding material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58142932A true JPS58142932A (en) | 1983-08-25 |
JPS6129616B2 JPS6129616B2 (en) | 1986-07-08 |
Family
ID=12193751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2644782A Granted JPS58142932A (en) | 1982-02-19 | 1982-02-19 | Preparation of phenolic resin molding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58142932A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59189159A (en) * | 1983-04-12 | 1984-10-26 | Tokai Rubber Ind Ltd | Phenolic resin extrusion composition |
-
1982
- 1982-02-19 JP JP2644782A patent/JPS58142932A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59189159A (en) * | 1983-04-12 | 1984-10-26 | Tokai Rubber Ind Ltd | Phenolic resin extrusion composition |
Also Published As
Publication number | Publication date |
---|---|
JPS6129616B2 (en) | 1986-07-08 |
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