JPS5849745A - Phenolic resin molding compound - Google Patents

Phenolic resin molding compound

Info

Publication number
JPS5849745A
JPS5849745A JP14744781A JP14744781A JPS5849745A JP S5849745 A JPS5849745 A JP S5849745A JP 14744781 A JP14744781 A JP 14744781A JP 14744781 A JP14744781 A JP 14744781A JP S5849745 A JPS5849745 A JP S5849745A
Authority
JP
Japan
Prior art keywords
molding
filler
phenolic resin
cylinder
fluidity
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
JP14744781A
Other languages
Japanese (ja)
Inventor
Yoshitaka Tagami
田上 義貴
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 JP14744781A priority Critical patent/JPS5849745A/en
Publication of JPS5849745A publication Critical patent/JPS5849745A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:The titled molding compound that is made by using mainly spheric form of inorganic filler, thus being suitable for the use in injection molding, because it keeps sufficient fluidity in the cylinder on molding, shows high thermal stability and rapidly solidifies after injected into the mold. CONSTITUTION:A phenolic resin of novolac or resol type or their mixture obtained by using an acid or alkali as a catalyst, is combined with a sphere-formed inorganic filler such as glass beads. As a filler, nonspheric one such as alumina, talc or glass fiber may be used, however, the content of the spheric filler is preferably higher than 50wt%. The friction heat caused by the rotation of the screw in the cylinder is reduced to delay the curing reactions and increase the fluidity of the resin. Thus, its molding operability is improved and at the same time, molding becomes operable even when the content of the filler is increased.

Description

【発明の詳細な説明】 本発明は、射出成形に遍したフェノール樹脂成形材料に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a phenolic resin molding material suitable for injection molding.

近年、プラスチックスの用途の拡大、需要の急増と共に
これSC対処すべく成形能率を向上させることが試みら
れている。熱可塑性樹脂−こおいては。
In recent years, with the expansion of the uses of plastics and the rapid increase in demand, attempts have been made to improve molding efficiency in order to cope with this SC problem. Thermoplastic resin - in this case.

古くから射出成形法が採用されほぼ満足すべき状況で成
形作業が行なわれている。一方、熱硬化性樹脂、とりわ
けフェノール樹脂成形材料に動いても、成形能率の向上
を図るべ〈従来の直圧成形から射出成形法への移行がな
されつつある。
Injection molding has been used for a long time, and molding operations have been carried out under almost satisfactory conditions. On the other hand, with the shift to thermosetting resins, especially phenolic resin molding materials, there is a shift from conventional direct pressure molding to injection molding in order to improve molding efficiency.

ところか、熱硬化性樹脂が成形される過程においては、
加熱加圧−こより樹脂の溶融流動化と硬化反応が同時に
始まり、この2つの現象が競争的に進行するため射出・
成形機のシリンダー内において樹脂を溶融さ讐る間I(
成形が不能8こなる場合がある。すなわち、シリンダー
内において成形材料は加熱された状態化あり、かつスク
リユウの回転による摩擦熱8乙よって成形材料の温度が
上昇して硬化反応が進行し流動性が失なわれ、遂には射
出成形が不可能把なるのである。
However, in the process of molding thermosetting resin,
Heat and pressure - melting and fluidization of the resin and hardening reaction begin simultaneously, and as these two phenomena progress competitively, injection and
While the resin is melted in the cylinder of the molding machine,
Molding may become impossible. In other words, the molding material is heated inside the cylinder, and the temperature of the molding material rises due to the frictional heat generated by the rotation of the screw, causing a curing reaction to proceed and loss of fluidity, which eventually leads to injection molding. It seems impossible.

このため、熱硬化性樹脂成形材料を射出成形に供するに
際しては、射出成形機シリンダーの温度を、成形材料が
溶融状態を呈する程度のできるだけ低い湿度に保って硬
化反応の進行を抑え。
For this reason, when subjecting a thermosetting resin molding material to injection molding, the temperature of the injection molding machine cylinder is kept at the lowest possible humidity at which the molding material exhibits a molten state to suppress the progress of the curing reaction.

一方では成形金型をできるだけ高温化保っておき、材料
が注入されると−1こ硬化が完°了するような成形条件
を採用している。しかし、シリンダ一温度を抑えても硬
化反応は徐々番ζ進行するものであり、シリンダー内で
の成形材料の滞留時間が長くなったり長時間連続成形、
を行なっていると、徐々1と樹脂の流動性が失なわれ、
遂には射出成形が不可能になる事態が生ずる。そこで、
射出成形用熱硬化性樹脂成形材料としては、比較的低温
であるシリンダー内では硬化反応が進行ぜず、すなわち
溶融安定性があり一旦金型内に注入されると急速、に硬
化反応を起こすような特性を有するものが望、まれるこ
と−こなる。
On the other hand, the molding mold is maintained at as high a temperature as possible, and molding conditions are adopted such that -1 temperature curing is completed when the material is injected. However, even if the cylinder temperature is suppressed, the curing reaction proceeds gradually, and the residence time of the molding material in the cylinder becomes longer, and continuous molding occurs over a long period of time.
While doing this, the resin gradually loses its fluidity.
Eventually, a situation arises in which injection molding becomes impossible. Therefore,
As a thermosetting resin molding material for injection molding, the curing reaction does not proceed in the cylinder at a relatively low temperature; in other words, it is melt stable and once injected into the mold, the curing reaction occurs rapidly. Things that have certain characteristics are desired and desirable.

従来、フェノール樹脂成形材料においても以上の目的を
達成するため番ζ可塑剤を多量に添加して低温流動性を
確保する方法などが試みられている。しかし、可塑剤を
多量化使用する方法にあっては、成形品の光沢、あるい
は他の諸性能が悪、くなる欠点を有し、樹脂化反応を初
期の段階門留めた成形材料を用いる方法においては。
Conventionally, in order to achieve the above-mentioned purpose, attempts have been made to add a large amount of plasticizer to phenolic resin molding materials to ensure low-temperature fluidity. However, the method of using a large amount of plasticizer has the disadvantage that the gloss of the molded product or other various properties deteriorates, and the method of using a molding material in which the resinization reaction is stopped at an early stage. In.

成形中の揮発分の発生が多く成形品にもカスが留ったも
のが生じやすい欠点を有する。
It has the disadvantage that a large amount of volatile matter is generated during molding, and molded products tend to have residue.

本発明は1以上のような事情に基づいてなされたもので
あり、従来の欠点を解消し、成形時シリンダー内では充
分な流動性を保持して熱的安定性か良<、シかも一旦金
型内に注入されると速やかに硬化するほぼ理想的な射出
成形用フェノール樹脂成形材料を提供することを目的と
するものである。
The present invention has been made based on one or more of the above circumstances, and it solves the conventional drawbacks, maintains sufficient fluidity in the cylinder during molding, and improves thermal stability. The object of the present invention is to provide a nearly ideal phenolic resin molding material for injection molding, which hardens quickly when injected into a mold.

本発明は、フェノール樹脂成形材料についてその流動挙
動と硬化挙動につい、て検討した結果。
The present invention is the result of studies on the flow behavior and curing behavior of phenolic resin molding materials.

無機質充填材を含ませたフェノール樹脂成形材料におい
て、主たる無機質充填材として球状のものを使用すれば
、はぼ目的を−成し得ることを見い出したのである。
It has been discovered that in a phenolic resin molding material containing an inorganic filler, if a spherical material is used as the main inorganic filler, the object can be achieved.

本発明で用いられるフェノール樹脂は、酸又はアルカリ
を触媒として得られるノボラック型或はレゾール型樹脂
のいずれでもよく、又これらの混合物でもよい。球状の
無機質充填材とは。
The phenol resin used in the present invention may be either a novolac type or resol type resin obtained using an acid or an alkali as a catalyst, or a mixture thereof. What is a spherical inorganic filler?

例えば球径jO〜100μのガラスピーズ等である。球
状の無機質充填材のほか化アルミナ。
For example, glass beads having a spherical diameter of jO to 100μ are used. Spherical inorganic filler and chemical alumina.

カラスパウダー、タルク、クレー、ガラス繊維。Karasu powder, talc, clay, glass fiber.

カーボンブラック等球状でない無機質充填材を含有させ
てもよく1球状のものは全充填材の500重量部上か望
ましい。
Non-spherical inorganic fillers such as carbon black may be included, and it is preferable that one spherical filler exceeds 500 parts by weight of the total filler.

本発明のフェノール樹脂成形材料は、上述したフェノー
ル樹脂及び無機質充填材を含むものであるが、これには
さら(内部離形剤を配合させることができる。内部離形
剤としては、ステアリン酸、パルミチン酸などの長鎖カ
ルボン酸。
The phenolic resin molding material of the present invention contains the above-mentioned phenolic resin and inorganic filler, but may also contain an internal mold release agent. Examples of the internal mold release agent include stearic acid, palmitic acid, long chain carboxylic acids such as;

ステアリン酸亜鉛、ステアリン酸カルシウムなどの長鎖
カルボン酸の金属塩、カルテワックス。
Metal salts of long-chain carboxylic acids such as zinc stearate and calcium stearate, Cartewax.

モンタンワックスなどのワックス類が挙げられる。また
、その他の添加剤としてr−アミノプロピルエトキシシ
ランなどのシランカップリング剤のような充填材の処理
剤、酸化アンチモン。
Examples include waxes such as montan wax. Other additives include filler treatment agents such as silane coupling agents such as r-aminopropylethoxysilane, and antimony oxide.

ハロゲン化物、リン化物などの難燃剤、各種顔料などの
従来公知の添加剤を配合してもよい。
Conventionally known additives such as flame retardants such as halides and phosphides, and various pigments may also be blended.

本発明のフェノール樹脂成形材料は、上述の原材料をロ
ール等の通常の方法で混練し粉砕すれば得ることができ
る。本発明では、主たる無機質充填材として球状のもの
を使用しているのテ、射出成形機シリンダー内でスクリ
エウ回転化よる摩擦熱の発生を少なくして硬化反応の進
行を抑え、樹脂の流動性を向上させて成形作業を改善で
きること化なる。それと同時に、従来無機質充填剤の配
合量を高くした場合、成形材料の流れが悪くなり成形魯
こ支障を来たしたか。
The phenolic resin molding material of the present invention can be obtained by kneading and pulverizing the above-mentioned raw materials using a conventional method such as using a roll. In the present invention, a spherical filler is used as the main inorganic filler, which reduces the generation of frictional heat due to the rotation of the screw in the cylinder of the injection molding machine, suppresses the progress of the curing reaction, and improves the fluidity of the resin. This means that molding operations can be improved. At the same time, in the past, when the amount of inorganic filler was increased, the flow of the molding material became poor, causing problems in molding.

本発明では無機質充填材の配合量が多くても成形作業を
可能にできる。
In the present invention, even if the amount of inorganic filler blended is large, the molding operation can be performed.

次暴こ1本発明の詳細な説明する。Next, a detailed explanation of the present invention will be given.

実施例1 塩酸触媒のノボラック型フェノール樹脂(軟化点95℃
)’11.0重量部暴【対してヘキサ1sllJ1部、
ガラスピーズ(球径10〜5oza)−3oo重量部、
炭酸カルシウムフO重量部、スピリットブラック3重量
部、    ′ステアリン酸2重量部を加えて、120
℃790℃のロールで3〜5分間加熱混練して成形材料
を得た。第1表暑【成形材料のゲルタイム、流動性瑯よ
び樹脂の軟化点の測定結果を示した。
Example 1 Hydrochloric acid catalyzed novolak phenol resin (softening point 95°C
)'11.0 parts by weight [for 1 sll J 1 part of hexa,
Glass peas (ball diameter 10-5 oza) - 30 parts by weight,
Add 120 parts by weight of calcium carbonate, 3 parts by weight of spirit black, and 2 parts by weight of stearic acid.
A molding material was obtained by heating and kneading with a roll at 790°C for 3 to 5 minutes. Table 1 shows the measurement results of the gel time of the molding material, the fluidity of the molding material, and the softening point of the resin.

なお、第1表化おいてゲルタイムとは成形材料のゲルタ
イムを示し、ブラベンダープラストグラフを用いて測定
したものである。又。
In addition, in Table 1, the gel time indicates the gel time of the molding material, which was measured using a Brabender plastograph. or.

流動性とは成形材料のスパイラルフローの値である。以
下の実施例においても全く同様にして各項目の測定を行
った。
Fluidity is the value of spiral flow of a molding material. In the following Examples, each item was measured in exactly the same manner.

実施例2 塩酸触媒のノボラック型フェノール樹脂(軟化点95℃
)110重量部に対してヘキサ16重量部、商品名マイ
クロドール(ヘキスト合成株式会社製、CaMg(Co
畠〕。
Example 2 Hydrochloric acid catalyzed novolak phenolic resin (softening point 95°C
) 110 parts by weight, 16 parts by weight of hexa, trade name Microdol (manufactured by Hoechst Gosei Co., Ltd., CaMg(Co
Hatake].

を主成分とする球径2〜6μ)300重量部、炭酸カル
シウム70重量部、スピリットブラック3重量部、ステ
アリン酸2重量部を加えて、120℃/90℃のロール
73〜5分間加熱混練して成形材料を得た。第1表に成
形材料のゲルタイム、流動性、および樹脂の軟化点の測
定結果を示した。
300 parts by weight of spheres with diameters of 2 to 6μ, the main components of which are 70 parts by weight of calcium carbonate, 3 parts by weight of spirit black, and 2 parts by weight of stearic acid, and heated and kneaded at 120°C/90°C for 73 to 5 minutes. A molding material was obtained. Table 1 shows the measurement results of the gel time, fluidity, and softening point of the molding material.

比較例 塩酸電媒のノボラック型フェノール樹脂(軟化点95℃
)110重量部に対してヘキサ15重量部、炭酸カルシ
ウム370重量部。
Comparative Example: Novolac type phenolic resin with hydrochloric acid as an electrolyte (softening point: 95°C)
) 110 parts by weight, 15 parts by weight of hexa, 370 parts by weight of calcium carbonate.

スピリットブラック3重量部、ステアリン酸2重量部を
加えて、120℃790℃のロール73〜5分間加熱混
練して成形材料を得た。
3 parts by weight of spirit black and 2 parts by weight of stearic acid were added, and the mixture was heated and kneaded with rolls at 120°C and 790°C for 5 minutes to obtain a molding material.

第1表番こ成形材料のゲルタイム、流動性、および樹脂
の軟化点の測定結果を示した。
Table 1 shows the measurement results of the gel time, fluidity, and softening point of the molding material.

第    1   表 第1表から1本発明の成形材料はゲル化までの時間が低
温では長く、つまりシリンダー内ての安定性がよく流動
性を長く維持てきることが了解される。この仁とは本発
明で用−する球状無機質充填材に特有なものであり、他
の無機物質ではこのような効果は認められなも1゜上述
のように本発明は、射出成形機シリンダー内での安定性
かより優れたものとなり、成形作業性を改善することが
できる点その工業的価値は極めて大なるものである。
Table 1 It can be seen from Table 1 that the molding material of the present invention takes a long time to gel at low temperatures, that is, it has good stability in the cylinder and maintains fluidity for a long time. This effect is unique to the spherical inorganic filler used in the present invention, and although such an effect is not observed with other inorganic materials, the present invention has the advantage of Its industrial value is extremely great, as it has better stability and improves molding workability.

Claims (1)

【特許請求の範囲】[Claims] 無機質充填材を含ませたフェノール樹脂成形材料におい
て、主たる無機質充填材として球状のものを用いたこと
を特徴とするフェノール樹脂成形材料。
A phenolic resin molding material containing an inorganic filler, characterized in that a spherical material is used as the main inorganic filler.
JP14744781A 1981-09-18 1981-09-18 Phenolic resin molding compound Pending JPS5849745A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14744781A JPS5849745A (en) 1981-09-18 1981-09-18 Phenolic resin molding compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14744781A JPS5849745A (en) 1981-09-18 1981-09-18 Phenolic resin molding compound

Publications (1)

Publication Number Publication Date
JPS5849745A true JPS5849745A (en) 1983-03-24

Family

ID=15430549

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14744781A Pending JPS5849745A (en) 1981-09-18 1981-09-18 Phenolic resin molding compound

Country Status (1)

Country Link
JP (1) JPS5849745A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008230627A (en) * 2007-03-16 2008-10-02 Dainippon Printing Co Ltd Packaging tube

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008230627A (en) * 2007-03-16 2008-10-02 Dainippon Printing Co Ltd Packaging tube

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