JPS60101148A - Production of thermosetting molding material - Google Patents

Production of thermosetting molding material

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Publication number
JPS60101148A
JPS60101148A JP20827083A JP20827083A JPS60101148A JP S60101148 A JPS60101148 A JP S60101148A JP 20827083 A JP20827083 A JP 20827083A JP 20827083 A JP20827083 A JP 20827083A JP S60101148 A JPS60101148 A JP S60101148A
Authority
JP
Japan
Prior art keywords
resin
molding material
mixture
glass fiber
thermosetting
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
JP20827083A
Other languages
Japanese (ja)
Inventor
Masae Yamada
山田 正栄
Tetsuo Aso
麻生 哲夫
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP20827083A priority Critical patent/JPS60101148A/en
Publication of JPS60101148A publication Critical patent/JPS60101148A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To increase the quantity to be discharged in a subsequent kneading stage by forming a less bulky mixture, by incorporating a glass fiber having a specified fiber length with a thermosetting resin. CONSTITUTION:5-75wt% glass fiber having a fiber length of 0.3-2mm. and other additives such as a filler, a catalyst, etc. are mixed with a thermosetting resin such as dillyl phthalate resin, phenolic resin or epoxy resin in a ribbon blender or a Henschel mixer. The resulting mixture having a high bulk density is kneaded in a screw extruder and extruded to obtain a thermosetting molding material.

Description

【発明の詳細な説明】 本発明は、熱硬化性成形材料の製造にあたって、混線の
前工程として行う各種原料の混合工程において、?Jモ
合物の嵩張りを小さくする方法を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a process for mixing various raw materials as a pre-crosstalk process in the production of thermosetting molding materials. The present invention provides a method for reducing the bulk of a J-Mo compound.

混合物の高張シを小さくすることによって、一定容積の
混合機によって混合できる1バツチあたシの混合量を多
くすることができる。また、スクリュー押出機で混合す
る場合には、スクリ=−1回転あたりの混合物の搬送量
を多くし、結果的に吐出量を増大せしめることができる
By reducing the hypertonicity of the mixture, it is possible to increase the amount of mixture per batch that can be mixed by a mixer with a constant volume. Furthermore, when mixing is performed using a screw extruder, the amount of the mixture conveyed per screw = -1 rotation can be increased, resulting in an increase in the amount of discharge.

本発明はこのような効果をもたらすものである。The present invention brings about such effects.

種々の熱硬化性成形材料の中で、例えばジアリルフタレ
ート樹脂成形材料は、ガラス繊維が多量に含有される場
合が多く 、 DM−GE、 DM−GF級では、50
重量−近く含有する場合が珍らしくない。また、充填材
として木粉、アスベスト、炭酸カルシウム等が多く用い
られてきたフェノール樹脂成形材料の場合でも、近年そ
の耐熱性といり特徴を生かし、自動車部品等の金属代替
用として検討されるようになり、よシ高い強度、寸法安
定性等を得るために、ガラス繊維を高充填するものが使
われるようになってきた。
Among various thermosetting molding materials, for example, diallyl phthalate resin molding materials often contain a large amount of glass fiber, and in the DM-GE and DM-GF grades, the glass fiber content is 50%.
It is not uncommon for the weight to be close to the same. In addition, even in the case of phenolic resin molding materials, which have often used wood flour, asbestos, calcium carbonate, etc. as fillers, in recent years they have been considered as metal substitutes for automobile parts, taking advantage of their heat resistance and other characteristics. In order to obtain higher strength, dimensional stability, etc., materials filled with glass fibers have come to be used.

従来、かかる熱硬化性成形材料に用いられるガラス繊維
は3〜6叫のものが主として用いられてきた。この長さ
はガラスロービングの切断の点での生産性、成形材料の
原料としての取シ扱い易さ、また強化材として必要な繊
維長などの種々の点で、それなシにバランスがとれた長
さではある。しかしながら、熱硬化性成形材料にガラス
繊維が高充填されるようになると、その製造にあたって
、このような長さのものには、重大な欠点があることが
明らかになった。すなわち、混練の前工程として、ガラ
ス繊維、樹脂、その他必要成分(離型剤、着色剤等)の
混合するに際してこのような長さのガラス繊維は、収束
がほぐれたものがからまりあい、いわゆる毛玉を作り、
しかもその毛玉自体の見掛密度が小さく、全体として非
常に高張シの大きい混合物となってしまうのである。か
かる現象の弊害として1バツチあたりの混合量が抑えら
れてしまうことが挙けられる。またスクリュー押出機へ
、このような混合物を供給してもいわゆる喰い込みが悪
く、少ない吐出量を受容せざるを得ないのである。かよ
うな現象の解決策の一つとして、毛玉を作らないような
非常に短繊維のガラス繊維を用いる方法が考えられる。
Conventionally, glass fibers of 3 to 6 types have been mainly used in such thermosetting molding materials. This length is well-balanced in terms of productivity in cutting the glass roving, ease of handling as a raw material for molding material, and fiber length required as a reinforcing material. It's the length. However, as thermosetting molding materials became highly filled with glass fibers, it became clear that such lengths had serious drawbacks in their manufacture. In other words, when mixing glass fibers, resin, and other necessary components (mold release agent, coloring agent, etc.) as a pre-kneading process, glass fibers of such length are untied and tangled, resulting in so-called Make a hairball,
Moreover, the apparent density of the fluff itself is low, resulting in a mixture that is extremely hypertonic as a whole. A disadvantage of this phenomenon is that the amount of mixture per batch is suppressed. Furthermore, even if such a mixture is supplied to a screw extruder, it is poorly penetrated, and a small discharge amount must be accepted. One possible solution to this phenomenon is to use very short glass fibers that do not form pilling.

しかし0.3 trm以下の短繊維のものでは、補強効
果が十分でなく得られた成形材料の機械強度が低下して
しまう。また、混合中の解繊を防ごうとして非常に収束
性の強いガラス繊維を用いた場合には、混練工程におい
て分散が不十分になったシ、あるいは、混練機に異常な
負荷がかかったりするので、これも好ましくない。
However, short fibers of 0.3 trm or less do not have a sufficient reinforcing effect and the mechanical strength of the resulting molding material decreases. Additionally, if glass fibers with very strong convergence properties are used to prevent fibrillation during mixing, dispersion may become insufficient during the kneading process, or an abnormal load may be placed on the kneader. So this is also not desirable.

本発明はこのような問題点を取シ除くために為されたも
のであり、0.3〜2胴のガラス繊維を用いて、高張シ
の少ない混合物を得ることを目的とする。
The present invention has been made to eliminate such problems, and aims to obtain a mixture with less hypertonicity by using 0.3 to 2 glass fibers.

以下にこれを詳しく述べる。This will be explained in detail below.

樹脂の種類は何等限定されるものではなく、粉末状で使
用に供される樹脂を用いての成形材料の製造に本発明を
用いることができる。各種原料の混合は、例えばりボン
プレンター、ニータ゛−、ヘンシェルなどの混合機が用
いられる。この工程において0.3〜2mmのガラス繊
維が他の各種原料とともに混合されるが、1〜2調で通
常の収束性のものが望ましい。このもの紘一部混合工程
で解繊するが、毛玉を作シに<<、混合物の高張シを大
きくしない。また、次の混線工程において何等不具合を
生ずるものでなく、得られる材料の機械強度も、よシ長
繊維のガラス繊維を用いた場合と同等である。添加Mは
、5〜75重量%の間で必要により任意に選ぶことが可
能であるが、望ましくは10〜70%である。10%以
下では補強効果が十分でなく、また70%以上では、成
形性その他の問題が生じる。ただし、繊維長、添加量と
もにここで述べたことに限定されるものではない。
The type of resin is not limited in any way, and the present invention can be used to produce a molding material using a resin that is used in powder form. For mixing the various raw materials, a mixer such as a Bonpreter, Niter, Henschel, etc. is used, for example. In this step, glass fibers of 0.3 to 2 mm are mixed together with various other raw materials, and it is desirable that the fibers have a 1 to 2 tone and normal convergence. Although this product partially defibrates in the mixing process, it does not cause pilling or increase the hypertonicity of the mixture. Further, no problems occur in the next cross-wire step, and the mechanical strength of the obtained material is equivalent to that of using long glass fibers. The amount of M to be added can be arbitrarily selected between 5 and 75% by weight, but is preferably 10 to 70%. If it is less than 10%, the reinforcing effect will not be sufficient, and if it is more than 70%, problems such as moldability will occur. However, both the fiber length and the amount added are not limited to those described here.

混線工程は、大別してロールまたはスクリュー押出(炭
によって行なわ)する。スクリュー押出機は、コニーダ
ーのよりな1軸のもの、或は2軸押用機が用いられる。
The mixing process can be broadly classified into roll or screw extrusion (carried out using charcoal). As the screw extruder, a single screw extruder such as a co-kneader or a twin screw extruder is used.

特にスクリュー押出機での製造において、本発明は効果
的である。押出機での熱硬化性成形材料の製造において
、押出機の能力がフルに生かされるならは理想的な状態
であるが、押出機に供給される混合物の高張シが大きい
と、スフIJ、−の回転数を上限に設定しても、極微か
しか喰い込まず、本来混練可能な量よりもはるかに低い
量の吐出量しか得られない。混合物の高張シによって吐
出量が決まってしまう状態であシ、理想的な運転状態と
は程遠い。これに対して本発明による方法に従えば、押
出機の可塑化能力、押出能力等、装置の能力をフルに発
揮でき、電力効率の点でも極めて有利になるのである。
The present invention is particularly effective in production using a screw extruder. In the production of thermosetting molding materials using an extruder, it would be an ideal situation if the capacity of the extruder could be fully utilized, but if the mixture supplied to the extruder has a high degree of hypertonicity, it would cause problems such as sulfur IJ, - Even if the rotational speed is set to the upper limit, only a very small amount of particles will be mixed in, and the amount of discharge will be much lower than the amount that can be kneaded. The discharge amount is determined by the hypertonicity of the mixture, which is far from an ideal operating condition. On the other hand, if the method according to the present invention is followed, the capabilities of the extruder, such as the plasticizing ability and extrusion ability, can be fully utilized, and it is extremely advantageous in terms of power efficiency.

混線の後は、押出造粒、或は粉砕のような通常用いられ
る方法で成形材料を得る。
After mixing, a molding material is obtained by a commonly used method such as extrusion granulation or pulverization.

以上のような製造方法によシ機械強度に優れたジアリル
フタレート樹脂、ポリエステル樹脂、フェノール樹脂、
エポキシ樹脂等の熱硬化性樹脂成形材料を効率良く製造
することが可能である。
Diaryl phthalate resin, polyester resin, phenol resin,
It is possible to efficiently produce thermosetting resin molding materials such as epoxy resins.

つぎに実施例と比較例を併せて述べる。Next, Examples and Comparative Examples will be described together.

実施例1及比較例1.2 インフタル酸系不飽、和ポリエステル樹脂 80重知知
:ジアリルフタレートプレポリマー 20 #炭酸カル
シウム 285 〃 ガラス繊維 100 # ステアリン酸亜鉛 10 N ジクミルパーオキサイド 5I 計 100重量部 上記配合においてガラス繊維を1.5 rrrm (実
施例1)、0.2胴(比較例1)、6mm(比較例2)
とした場合の混合物の高張シ、スクリュー押出機での吐
出量、得られた成形材料の曲げ強さは表1の通シであっ
た。比較例2では強度が低く、比較例3では吐出量が極
めて小さいという欠点が見られる。
Example 1 and Comparative Example 1.2 Inphthalic acid-based unsaturated, Japanese polyester resin 80 weight Chichi: Diallyl phthalate prepolymer 20 #Calcium carbonate 285 Glass fiber 100 #Zinc stearate 10 N Dicumyl peroxide 5I Total 100 weight In the above formulation, the glass fiber was 1.5 rrrm (Example 1), 0.2 mm (Comparative Example 1), 6 mm (Comparative Example 2)
The high tensile strength of the mixture, the discharge amount in the screw extruder, and the bending strength of the obtained molding material were as shown in Table 1. Comparative Example 2 has low strength, and Comparative Example 3 has drawbacks such as extremely small discharge amount.

表1 注)混合機: 1004ニーダ−1o分スクリj、−押
出機: 2軸(50開鉾)、300 rpm実施例2、
比較例3 ジアリルフタレートプレポリマー 100 置方部ガラ
ス繊維 75 炭酸カルシウム 20 ステアリン酸亜鉛 25 # ジクミルパーオキサイド 2.5’1 計 200 上記配合においてガラス繊維を1.5 mm (実施例
2)、3M(比較例3)とした場合の混合物の高張シ、
スクリュー押出機での吐出量、得られた成形材料の曲げ
強さは表2の通シであった。比較例3では、吐出量が極
めて小さいという欠点が見られた。
Table 1 Note) Mixer: 1004 kneader - 1o minute screw j, - Extruder: 2 screws (50 openings), 300 rpm Example 2,
Comparative Example 3 Diallyl phthalate prepolymer 100 Glass fiber 75 Calcium carbonate 20 Zinc stearate 25 # Dicumyl peroxide 2.5'1 Total 200 In the above formulation, glass fiber was added to a thickness of 1.5 mm (Example 2), 3M (Comparative Example 3) Hypertonicity of the mixture,
The discharge amount in the screw extruder and the bending strength of the obtained molding material were as shown in Table 2. Comparative Example 3 had a drawback that the discharge amount was extremely small.

表2 LE) 17t+合u% : 1001= I” 10
分スクリュー押出機: コニーダー(PR−46)、6
0rpm/iテ許出p口人 住友ベークライト株式会社
Table 2 LE) 17t+total u%: 1001=I” 10
Minute screw extruder: Co-kneader (PR-46), 6
0rpm/item Sumitomo Bakelite Co., Ltd.

Claims (1)

【特許請求の範囲】 (1)ガラス9:維で強化した熱硬化性成形材料を製造
するにあたってガラス繊維長が0.3〜2酊であるとと
を特徴とする熱硬化性成形材料の製造方法(2)ガラス
繊維の疹加せが5〜75重量%である特許請求範囲第1
項記載の熱硬化性成形材料の製造方法 (3)ガラス繊維、樹脂その他必要成分の混線がスクリ
ュー押出機によって行われる特許請求範囲第1項又は第
2項記載の熱硬化性成形材料の製造方法
[Claims] (1) Glass 9: Production of a thermosetting molding material reinforced with fibers, characterized in that the glass fiber length is 0.3 to 2. Method (2) Claim 1 in which the addition of glass fiber is 5 to 75% by weight
(3) The method for producing a thermosetting molding material according to Claim 1 or 2, wherein the mixing of glass fibers, resins, and other necessary components is carried out using a screw extruder.
JP20827083A 1983-11-08 1983-11-08 Production of thermosetting molding material Pending JPS60101148A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20827083A JPS60101148A (en) 1983-11-08 1983-11-08 Production of thermosetting molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20827083A JPS60101148A (en) 1983-11-08 1983-11-08 Production of thermosetting molding material

Publications (1)

Publication Number Publication Date
JPS60101148A true JPS60101148A (en) 1985-06-05

Family

ID=16553458

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20827083A Pending JPS60101148A (en) 1983-11-08 1983-11-08 Production of thermosetting molding material

Country Status (1)

Country Link
JP (1) JPS60101148A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5462244A (en) * 1977-10-27 1979-05-19 Mitsubishi Chem Ind Ltd Thermosetting resin composition for molding
JPS5478741A (en) * 1977-12-06 1979-06-23 Tokuyama Soda Co Ltd Thickener
JPS564640A (en) * 1979-06-22 1981-01-19 Matsushita Electric Works Ltd Thermosetting resin composition
JPS57212254A (en) * 1981-06-23 1982-12-27 Hitachi Chem Co Ltd Preparation of thermosetting resin molding material

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5462244A (en) * 1977-10-27 1979-05-19 Mitsubishi Chem Ind Ltd Thermosetting resin composition for molding
JPS5478741A (en) * 1977-12-06 1979-06-23 Tokuyama Soda Co Ltd Thickener
JPS564640A (en) * 1979-06-22 1981-01-19 Matsushita Electric Works Ltd Thermosetting resin composition
JPS57212254A (en) * 1981-06-23 1982-12-27 Hitachi Chem Co Ltd Preparation of thermosetting resin molding material

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