JP3824398B2 - Phenolic resin molding material - Google Patents
Phenolic resin molding material Download PDFInfo
- Publication number
- JP3824398B2 JP3824398B2 JP24682497A JP24682497A JP3824398B2 JP 3824398 B2 JP3824398 B2 JP 3824398B2 JP 24682497 A JP24682497 A JP 24682497A JP 24682497 A JP24682497 A JP 24682497A JP 3824398 B2 JP3824398 B2 JP 3824398B2
- Authority
- JP
- Japan
- Prior art keywords
- molding material
- phenolic resin
- strength
- resin molding
- weight
- 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 - Fee Related
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Description
【0001】
【発明の属する技術分野】
本発明は、衝撃強度、曲げ強度等の機械的強度に優れたフェノール樹脂成形材料に関するものである。
【0002】
【従来の技術】
フェノール樹脂成形材料は耐熱性、寸法安定性、成形性等に優れ、自動車、電気・電子等の基幹産業分野で長期にわたり使用されてきた実績がある。特に最近では、金属製の部品を、ガラス繊維で強化した高強度のフェノール樹脂成形品に置換することで、大幅なコストダウンが可能となることから、積極的な代替検討が行われている。しかしながら、ガラス繊維で強化した高強度のフェノール樹脂成形材料でもシャルピー衝撃強さが約5KJ/m2 、曲げ強さが約200MPaが限界であり、更に金属からの代替を進めるには、機械的強度のレベルアップが必要とされている。機械的強度向上の試みは以前から数多くなされており、衝撃強度に関しては、特開平3―137151号公報にあるような樹脂をNBR変性する技術により強度向上がはかれた例もあるが、衝撃強度、静的強度(曲げ強さ等)ともに向上させることは難しいのが現状である。
【0003】
【発明が解決しようとする課題】
本発明は、従来のガラス繊維で強化した高強度フェノール樹脂成形材料の機械的強度の限界を超えるべく種々検討した結果、フェノール樹脂に、ガラス繊維、その他の材料の配合時にD−ソルビトールを添加することにより衝撃強度、曲げ強さとも向上するという知見を得て、本発明を完成するに至った。
【0004】
【課題を解決するための手段】
本発明は、成形材料全体に対して、ノボラック型フェノール樹脂を30〜60重量%含有し、ガラス繊維を30〜60重量%、添加剤としてD−ソルビトールを1〜4重量%含有することを特徴とするフェノール樹脂成形材料に関するものである。
【0005】
本発明に用いられるノボラック型フェノール樹脂は特に限定されるものではないが、数平均分子量が800〜1000で、フェノール核に対するオルソ/パラ結合比が1以下のものを用いると、成形材料化段階での作業性、及び成形性(特に射出成形性)、得られた成形物の特性が比較的良好であるので好ましく、硬化剤としてヘキサメチレンテトラミンをノボラック型フェノール樹脂に対し、15〜20重量%配合するのが好ましい。
【0006】
またガラス繊維については、繊維径が10〜15μm、繊維長が1〜3mmのものを使用することが成形材料化段階での作業性、得られた成形物の強度が比較的良好であり、配合量については成形材料全体に対し30〜60重量%が好ましい。30重量%未満では満足し得る強度が得られにくいこと、寸法変化が大きくなることなど、60重量%を越えると成形材料化段階での作業性が困難であること、成形品の強度低下につながることなどから、30〜60重量%にするのが好ましいのである。
【0007】
本発明の目的である機械的強度向上のために用いるD−ソルビトールについては、その添加量は成形材料全体に対して1〜4重量%であることが好ましい。この理由は1重量%未満では、強度向上の効果が低く、4重量%を越えると強度低下につながるからである。D−ソルビトールを使用した理由については、融点が約90℃であり、成形材料化段階で溶融し可塑剤的な効果を発揮すること、溶融したときの粘性が比較的低く分散性が良好であることなどが挙げられる。D−ソルビトールの作用については明らかではないが、樹脂との相溶性に優れており、ガラス繊維のような無機基材と濡れ性の良い官能基(−OH基)を持っておりカップリング剤的な作用があるものと推定される。特に、−OH基を単量体中に6個と多数持っていることでこの効果がより大きくなるものと考えられる。
【0008】
本発明のフェノール樹脂成形材料を得る場合、上記原料を均一に混合後、ロール、コニーダ、二軸押出し機等の混練機単独又はロールと他の混合機との組み合わせで加熱混練し、粉砕して得られる。本発明のフェノール樹脂成形材料は機械的強度が優れており、自動車、電気・電子等の金属部品の代替に適用できる。
【0009】
【実施例】
以下、実施例により本発明を説明する。実施例及び比較例の配合と特性を表1に示す。特性評価用試験片はトランスファー成形により作製し、評価方法はJISに基づいて行った。
【0010】
【表1】
なお、ノボラック型フェノール樹脂は、オルソ/パラ結合比0.8、数平均分子量900のものを使用した。
【0011】
【発明の効果】
以上の実施例及び比較例から明らかなように、本発明のフェノール樹脂成形材料は、衝撃強度、静的強度のような機械的強度に優れ、自動車、電気・電子分野における金属代替を大幅に促進するものである。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a phenol resin molding material excellent in mechanical strength such as impact strength and bending strength.
[0002]
[Prior art]
Phenolic resin molding materials are excellent in heat resistance, dimensional stability, moldability, etc., and have been used for a long time in key industries such as automobiles and electrical / electronics. In particular, since replacement of metal parts with high-strength phenolic resin products reinforced with glass fibers enables a significant cost reduction, active alternative studies are being conducted. However, even for high-strength phenolic resin molding materials reinforced with glass fibers, the Charpy impact strength is about 5 KJ / m 2 and the bending strength is about 200 MPa. Level up is required. Many attempts have been made to improve the mechanical strength. Regarding the impact strength, there is an example in which the strength is improved by a technique for NBR modification of a resin as disclosed in JP-A-3-137151. At present, it is difficult to improve both static strength (bending strength, etc.).
[0003]
[Problems to be solved by the invention]
In the present invention, as a result of various studies to exceed the limit of the mechanical strength of the conventional high strength phenol resin molding material reinforced with glass fiber, D-sorbitol is added to the phenol resin at the time of blending glass fiber and other materials. As a result, the inventors have obtained the knowledge that both the impact strength and the bending strength are improved, and have completed the present invention.
[0004]
[Means for Solving the Problems]
The present invention contains 30-60% by weight of novolac-type phenolic resin, 30-60% by weight of glass fiber, and 1-4% by weight of D-sorbitol as an additive, based on the entire molding material. It relates to a phenolic resin molding material.
[0005]
The novolak type phenolic resin used in the present invention is not particularly limited. However, when a resin having a number average molecular weight of 800 to 1000 and an ortho / para bond ratio with respect to the phenol nucleus of 1 or less is used, at the stage of forming a molding material. Workability, moldability (particularly injection moldability), and the properties of the resulting molded product are relatively good, and it is preferable that hexamethylenetetramine as a curing agent is blended in an amount of 15 to 20% by weight based on the novolac type phenol resin It is preferable to do this.
[0006]
For glass fibers, use of fibers having a fiber diameter of 10 to 15 μm and fiber lengths of 1 to 3 mm is relatively good in workability at the stage of forming a molding material, and the strength of the obtained molded product is relatively good. The amount is preferably 30 to 60% by weight based on the entire molding material. If it is less than 30% by weight, it is difficult to obtain satisfactory strength, and the dimensional change becomes large. In view of the above, it is preferably 30 to 60% by weight.
[0007]
The D-sorbitol used for improving the mechanical strength, which is the object of the present invention, is preferably added in an amount of 1 to 4% by weight based on the entire molding material. This is because if the amount is less than 1% by weight, the effect of improving the strength is low, and if it exceeds 4% by weight, the strength is reduced. Regarding the reason for using D-sorbitol, the melting point is about 90 ° C., it melts at the molding material stage and exerts a plasticizer effect, the viscosity when melted is relatively low, and the dispersibility is good. And so on. Although the action of D-sorbitol is not clear, it has excellent compatibility with the resin, has an inorganic base material such as glass fiber, and a functional group (-OH group) with good wettability, which is like a coupling agent. It is estimated that there is an effect. In particular, it is considered that this effect is increased by having as many as six —OH groups in the monomer.
[0008]
When obtaining the phenol resin molding material of the present invention, after uniformly mixing the above raw materials, knead and pulverize with a kneader such as a roll, a kneader, a twin screw extruder alone or a combination of a roll and another mixer. can get. The phenolic resin molding material of the present invention is excellent in mechanical strength and can be applied to substitutes for metal parts such as automobiles and electric / electronics.
[0009]
【Example】
Hereinafter, the present invention will be described by way of examples. Table 1 shows the composition and characteristics of Examples and Comparative Examples. The test piece for characteristic evaluation was produced by transfer molding, and the evaluation method was performed based on JIS.
[0010]
[Table 1]
As the novolac type phenol resin, one having an ortho / para bond ratio of 0.8 and a number average molecular weight of 900 was used.
[0011]
【The invention's effect】
As is clear from the above examples and comparative examples, the phenolic resin molding material of the present invention is excellent in mechanical strength such as impact strength and static strength, and greatly promotes metal substitution in the automobile and electrical / electronic fields. To do.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24682497A JP3824398B2 (en) | 1997-09-11 | 1997-09-11 | Phenolic resin molding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24682497A JP3824398B2 (en) | 1997-09-11 | 1997-09-11 | Phenolic resin molding material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH1180499A JPH1180499A (en) | 1999-03-26 |
JP3824398B2 true JP3824398B2 (en) | 2006-09-20 |
Family
ID=17154246
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24682497A Expired - Fee Related JP3824398B2 (en) | 1997-09-11 | 1997-09-11 | Phenolic resin molding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3824398B2 (en) |
-
1997
- 1997-09-11 JP JP24682497A patent/JP3824398B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH1180499A (en) | 1999-03-26 |
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