JPH06192544A - Phenolic resin molding material - Google Patents
Phenolic resin molding materialInfo
- Publication number
- JPH06192544A JPH06192544A JP34668192A JP34668192A JPH06192544A JP H06192544 A JPH06192544 A JP H06192544A JP 34668192 A JP34668192 A JP 34668192A JP 34668192 A JP34668192 A JP 34668192A JP H06192544 A JPH06192544 A JP H06192544A
- Authority
- JP
- Japan
- Prior art keywords
- phenol resin
- molding material
- mechanical strength
- resin molding
- blisters
- 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
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】
【構成】 フェノール樹脂、及び充填材として有機質充
填材と無機質充填材とを含有するフェノール樹脂成形材
料であって、数平均分子量が800〜1200のノボラ
ック型フェノール樹脂を主成分とし、有機充填材として
繊維長2mmの天然繊維を含有し、無機充填材としてタ
ルク、クレー、水酸化アルミニウム、炭酸カルシウ
ム,、炭酸マグネシウムから選ばれた一種以上を含有す
るフェノール樹脂成形材料。
【効果】 常温時、加熱時の機械的強度が従来の成形材
料に比べ優れている。更に、速硬化性でフクレが無いた
め、フクレによる寸法変化を起こさず、寸法安定性に優
れ、なお且つ成形性の良好な成形材料である。(57) [Summary] [Structure] A phenol resin molding material containing a phenol resin and an organic filler and an inorganic filler as fillers, the main component of which is a novolac type phenol resin having a number average molecular weight of 800 to 1200. A phenol resin molding material containing natural fiber having a fiber length of 2 mm as an organic filler and one or more selected from talc, clay, aluminum hydroxide, calcium carbonate, and magnesium carbonate as an inorganic filler. [Effect] Mechanical strength at room temperature and at heating is superior to that of conventional molding materials. Furthermore, since it is fast-curing and has no blisters, it does not cause dimensional changes due to blisters, is excellent in dimensional stability, and has good moldability.
Description
【0001】[0001]
【産業上の利用分野】本発明は機械強度、特に加熱時に
おける機械強度に優れ、フクレが無くフクレによる寸法
変化の無い寸法安定性に優れたフェノール樹脂成形材料
に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a phenol resin molding material which is excellent in mechanical strength, particularly in heating, and which is excellent in dimensional stability without blister and dimensional change due to blister.
【0002】[0002]
【従来の技術】従来機械強度を大きくする手段として、
繊維長の長い天然繊維、例えばパルプや粉砕布を配合す
ることが行われている。パルプや粉砕布をし配合した場
合配合前に比べ機械強度は一割程向上する。しかし、パ
ルプや粉砕布は、混練時の作業性を悪くしたり、成形時
に流れにくくなったり、充填不良を起こしやすいため、
配合量に限界がある。また加熱時の機械強度はそれほど
向上しないという欠点があった。また、ガラス繊維を配
合することで機械強度は格段に向上する。しかしガラス
繊維を用いた場合耐磨耗性が悪いという欠点がある。更
に、コスト面でも高価なものとなり好ましくない。寸法
安定性についても従来、硬化が緩やかなため、フクレが
生じやすく、その結果、フクレによる変形を生じ、寸法
変化を生じていた。2. Description of the Related Art Conventionally, as means for increasing mechanical strength,
Natural fibers having a long fiber length such as pulp and crushed cloth are blended. When pulp or crushed cloth is blended, the mechanical strength is improved by about 10% compared to before blending. However, since pulp and crushed cloth deteriorate the workability during kneading, make it difficult to flow at the time of molding, and easily cause poor filling,
There is a limit to the blending amount. Further, there is a drawback that the mechanical strength during heating does not improve so much. Further, the mechanical strength is remarkably improved by incorporating glass fiber. However, when glass fibers are used, there is a drawback that abrasion resistance is poor. Further, it is not preferable because it is expensive in terms of cost. Regarding dimensional stability, conventionally, gradual hardening is liable to occur, so that blisters are likely to occur, resulting in deformation due to blisters and dimensional changes.
【0003】[0003]
【発明が解決しようとする課題】本発明は、従来の上記
のような問題点を解決するため、種々の検討の結果なさ
れたもので、その目的とするところは、機械強度、特に
加熱時の機械強度に優れ且つ、寸法安定性に優れたフェ
ノール樹脂成形材料を提供することにある。SUMMARY OF THE INVENTION The present invention has been made as a result of various studies in order to solve the above-mentioned problems of the prior art, and its object is to obtain mechanical strength, particularly when heating. It is to provide a phenol resin molding material having excellent mechanical strength and dimensional stability.
【0004】[0004]
【課題を解決するための手段】本発明は、フェノール樹
脂、及び充填材として有機質充填材と無機質充填材とを
含有するフェノール樹脂成形材料であって、フェノール
樹脂は数平均分子量が800〜1200のノボラック型
フェノール樹脂を主成分とし、有機充填材として繊維長
0.5〜5mmの天然繊維を含有し、無機充填材として
タルク、クレー、水酸化アルミニウム、炭酸カルシウ
ム、炭酸マグネシウムから選ばれた一種以上を含有する
ことを特徴とするフェノール樹脂成形材料である。本発
明において用いられるフェノール樹脂は、数平均分子量
800〜1200、好ましくは900〜1100であ
る。数平均分子量800以下では機械強度、とりわけ加
熱時の機械強度の向上は望めない。また数平均分子量が
1200以上では、フェノール樹脂の軟化点が高く、均
一に混練できなかったり、溶融粘度が高くなってしまう
ため流動性に乏しくなり、成形できないため好ましくな
い。更に、上記フェノール樹脂は、フェノール核に結合
するメチレン結合において、オルソ結合対パラ結合の比
が0.6〜1.2であるノボラック型フェノール樹脂が硬
化性、機械的強度の点で好ましい。The present invention is a phenol resin molding material containing a phenol resin and an organic filler and an inorganic filler as fillers, wherein the phenol resin has a number average molecular weight of 800 to 1200. One or more selected from talc, clay, aluminum hydroxide, calcium carbonate, and magnesium carbonate as the inorganic filler, containing novolac-type phenolic resin as the main component, organic fillers containing 0.5-5 mm fiber length natural fibers. It is a phenol resin molding material characterized by containing. The phenol resin used in the present invention has a number average molecular weight of 800 to 1200, preferably 900 to 1100. If the number average molecular weight is 800 or less, improvement in mechanical strength, particularly mechanical strength during heating, cannot be expected. Further, when the number average molecular weight is 1200 or more, the softening point of the phenol resin is high, so that the resin cannot be uniformly kneaded, or the melt viscosity becomes high, resulting in poor fluidity and unfavorable molding. Further, the above-mentioned phenol resin is preferably a novolac type phenol resin in which the ratio of ortho bond to para bond in the methylene bond bonded to the phenol nucleus is 0.6 to 1.2, from the viewpoint of curability and mechanical strength.
【0005】充填材は、有機質充填材として繊維長 0.
5〜5mmの有機天然繊維を用いる。かかる有機天然繊
維としては、綿、麻などの繊維又はこれらの織物の切断
物あるいは粉砕物、各種パルプなどであり、異種材質の
ものを二種以上併用することもできる。これらは繊維長
0.1〜5mmが好ましく、更に好ましくは0.5〜2m
mである。 0.1mm以下では成形品の機械強度の向上
が小さく、5mm以上では機械強度は向上するが、材料
化した際の解繊及び分散度が悪く、成形材料のかさばり
が大きくなり好ましくない。また無機充填材としては、
タルク、クレー、水酸化アルミニウム、炭酸カルシウ
ム、炭酸マグネシウムから選ばれた一種又は二種以上を
用いる。これらの無機充填材の使用により耐熱性が向上
し、加熱時の機械強度の低下を軽減することができ、更
に、表面硬度が付与され、成形品のフクレによる寸法変
化を無くすることができる。The filler is an organic filler having a fiber length of 0.
5-5 mm organic natural fibers are used. Examples of such organic natural fibers include fibers such as cotton and hemp, cut or crushed products of these fabrics, various pulps, and the like, and two or more kinds of different materials can be used in combination. These fibers preferably have a fiber length of 0.1 to 5 mm, more preferably 0.5 to 2 m.
m. If the thickness is 0.1 mm or less, the mechanical strength of the molded product is not improved, and if it is 5 mm or more, the mechanical strength is improved. As the inorganic filler,
One or more selected from talc, clay, aluminum hydroxide, calcium carbonate and magnesium carbonate are used. By using these inorganic fillers, the heat resistance is improved, the reduction in mechanical strength during heating can be reduced, and further, the surface hardness is imparted, and the dimensional change due to blister of the molded product can be eliminated.
【0006】これらの充填材の好ましい配合量は、フェ
ノール樹脂100重量部に対して、有機天然繊維10〜
50重量部、無機充填材15〜40重量部である。有機
天然繊維が10重量部以下では成形品の機械強度が向上
せず、50重量部以上では、成形材料のかさばりが大き
くなり、成形材料化が困難になるなどの問題が生じるた
め好ましくない。また、無機充填材が15重量部以下で
は、耐熱性が向上せず、加熱時の機械強度及び表面硬度
が低下してしまう。40重量部以上では、成形性が低下
し、成形物表面にボイドが生じやすく、好ましくない。
このような充填材の組み合わせにおいて、従来のフェノ
ール樹脂成形材料に比べ機械強度、特に加熱時の機械強
度及び寸法安定性に優れた成形材料を得る。また、フェ
ノール樹脂組成物に対して必要により、硬化触媒、滑
剤、着色剤等を配合して加熱混練することにより、成形
材料化する。The preferred blending amount of these fillers is 10 to 10 parts by weight of the organic resin and 100 parts by weight of the phenol resin.
50 parts by weight and 15 to 40 parts by weight of inorganic filler. When the amount of the organic natural fiber is 10 parts by weight or less, the mechanical strength of the molded product is not improved, and when it is 50 parts by weight or more, the bulkiness of the molding material becomes large, and it becomes difficult to form the molding material. Further, if the amount of the inorganic filler is 15 parts by weight or less, the heat resistance is not improved, and the mechanical strength and surface hardness during heating are reduced. When it is 40 parts by weight or more, the moldability is deteriorated and voids are easily generated on the surface of the molded product, which is not preferable.
With such a combination of fillers, a molding material is obtained which has excellent mechanical strength, especially mechanical strength and dimensional stability during heating, as compared with conventional phenol resin molding materials. If necessary, a curing catalyst, a lubricant, a coloring agent, etc. are added to the phenol resin composition, and the mixture is heated and kneaded to obtain a molding material.
【0007】[0007]
【作用】本発明のフェノール樹脂成形材料は、フェノー
ル樹脂の主成分として、数平均分子量が800〜120
0の比較的高分子量のノボラック型フェノール樹脂を用
いることにより、硬化後の樹脂に架橋間鎖長が長く、従
来のフェノール樹脂に比べ脆くない靱性に優れた特性を
付与できる。更に繊維長の長い有機天然繊維を配合する
ことにより機械強度を更に向上できる。また上記の無機
充填材を配合して耐熱性を付与することにより加熱時の
機械強度が向上する。更にこれら無機充填材の効果で表
面硬度が増し、フクレの発生を抑制し寸法安定性の良い
成形物を得ることができる。The phenol resin molding material of the present invention has a number average molecular weight of 800 to 120 as the main component of the phenol resin.
By using a relatively high molecular weight novolac type phenolic resin having a molecular weight of 0, the cured resin has a long inter-crosslinking chain length and can be imparted with characteristics that are not brittle and have excellent toughness as compared with conventional phenolic resins. Furthermore, the mechanical strength can be further improved by blending an organic natural fiber having a long fiber length. Further, by blending the above-mentioned inorganic filler to impart heat resistance, mechanical strength during heating is improved. Furthermore, the surface hardness is increased by the effect of these inorganic fillers, and the formation of blisters can be suppressed, and a molded product with good dimensional stability can be obtained.
【0008】[0008]
【実施例】次に本発明を実施例及び比較例に基づいて説
明する。ここで「部」は「重量部」を示す。表1に示す
材料及び配合にて、加熱ロールにより混練して、フェノ
ール樹脂成形材料を得た。EXAMPLES Next, the present invention will be explained based on Examples and Comparative Examples. Here, "part" means "part by weight". The materials and formulations shown in Table 1 were kneaded with a heating roll to obtain a phenol resin molding material.
【表1】 [Table 1]
【0009】比較例1は実施例1のノボラック型フェノ
ール樹脂を数平均分子量800以下のものに代えた場合
である。比較例2は実施例1のノボラック型フェノール
樹脂を数平均分子量1200以上のものに代えた場合で
ある。比較例3は、実施例1のクレーを粉砕布及び木粉
に置換え、クレーを配合しない場合である。各実施例及
び比較例で得られた成形材料について、常温時(25
℃)と加熱時(120℃)の曲げ強さ、シャルピー衝撃
強さ、、硬化性(フクレの生じない最小硬化時間)を測
定した。得られた結果を表2に示す。Comparative Example 1 is a case where the novolac type phenol resin of Example 1 is replaced with a resin having a number average molecular weight of 800 or less. Comparative Example 2 is a case where the novolac type phenol resin of Example 1 is replaced with a resin having a number average molecular weight of 1200 or more. Comparative Example 3 is a case where the clay of Example 1 is replaced with a crushed cloth and wood flour, and no clay is blended. The molding materials obtained in each of the examples and comparative examples were tested at room temperature (25
C.) and heating (120.degree. C.) flexural strength, Charpy impact strength, and curability (minimum curing time without blistering) were measured. The obtained results are shown in Table 2.
【0010】[0010]
【表2】 [Table 2]
【0011】〔測定方法〕 (1) 曲げ強さ、シャルピー衝撃強さ:JIS K 6911 に準
じて測定した。 (2) 120℃での曲げ強さ:雰囲気を120℃で30分
間保った後、120℃中で上記と同様な方法で測定し
た。 (3) 充填性:100×5×2mmの評価用金型を180℃
とし、長さ(100mm)方向から射出成形(射出圧力 1
250kgf/cm2 )し、充填性の良否を判定した。 (4) フクレのでない最小硬化時間:金型を180℃と
し、射出成形により60φ×4mm厚の試験片を成形し、
硬化時間を20秒から1秒ずつ短縮する。フクレの発生
した1秒前の硬化時間をフクレの出ない最少硬化時間と
する。フクレはマイクロメーターで成形品の厚みを測定
し、所定厚みより 0.05mm越えたときをフクレとす
る。[Measuring method] (1) Bending strength, Charpy impact strength: Measured according to JIS K 6911. (2) Bending strength at 120 ° C .: The atmosphere was kept at 120 ° C. for 30 minutes and then measured at 120 ° C. by the same method as above. (3) Fillability: 180 ° C. with an evaluation mold of 100 × 5 × 2 mm
And injection molding from the length (100 mm) direction (injection pressure 1
250 kgf / cm 2 ) and the quality of the filling property was judged. (4) Minimum curing time without blistering: The mold is set to 180 ° C., a test piece of 60φ × 4 mm thickness is molded by injection molding,
Curing time is reduced from 20 seconds by 1 second. The curing time 1 second before the occurrence of blisters is the minimum curing time without blistering. For blister, measure the thickness of the molded product with a micrometer, and bulge when the thickness exceeds the specified thickness by 0.05 mm.
【0012】実施例1〜3で得られた成形材料について
は、常温及び加熱時でも高い曲げ強さで保持し、衝撃強
さも高く優れた機械強度を有している。更に、成形性が
良好であり、速硬化性でフクレの無い、フクレによる寸
法変化を生じない成形品が得られる。比較例1は、成形
性は良好であるが、機械強度及び硬化性に劣る。比較例
2は高い機械強度を有するが、充填性悪く、成形性が劣
る。比較例3は、常温での機械強度は高いものの加熱時
の曲げ強さが劣り、また成形性及び硬化性も低下する。The molding materials obtained in Examples 1 to 3 retain a high bending strength even at room temperature and at the time of heating and have a high impact strength and excellent mechanical strength. Further, it is possible to obtain a molded product which has good moldability, is fast-curing, has no blisters, and does not cause dimensional changes due to blisters. In Comparative Example 1, the moldability is good, but the mechanical strength and curability are poor. Comparative Example 2 has high mechanical strength, but poor filling properties and poor moldability. In Comparative Example 3, the mechanical strength at room temperature is high, but the bending strength at the time of heating is poor, and the moldability and curability are also reduced.
【0013】[0013]
【発明の効果】以上の実施例からも明らかなように、本
発明のフェノール樹脂成形材料は、常温時、加熱時の機
械的強度が従来の成形材料に比べ優れている。更に、速
硬化性でフクレが無いため、フクレによる寸法変化を起
こさず、寸法安定性に優れ、なお且つ成形性の良好な成
形材料である。As is clear from the above examples, the phenolic resin molding material of the present invention is superior in mechanical strength to the conventional molding material at room temperature and at heating. Furthermore, since it is fast-curing and has no blisters, it does not cause dimensional changes due to blisters, is excellent in dimensional stability, and has good moldability.
Claims (1)
質充填材と無機質充填材とを含有するフェノール樹脂成
形材料であって、フェノール樹脂は数平均分子量が80
0〜1200のノボラック型フェノール樹脂を主成分と
し、有機充填材として繊維長 0.5〜5mmの天然繊維
を含有し、無機充填材としてタルク、クレー、水酸化ア
ルミニウム、炭酸カルシウム、炭酸マグネシウムから選
ばれた一種以上を含有することを特徴とするフェノール
樹脂成形材料。1. A phenol resin molding material containing a phenol resin and an organic filler and an inorganic filler as fillers, wherein the phenol resin has a number average molecular weight of 80.
Main component is 0-1200 novolac type phenolic resin, natural fiber with fiber length 0.5-5mm is contained as organic filler, and inorganic filler is selected from talc, clay, aluminum hydroxide, calcium carbonate, magnesium carbonate. A phenolic resin molding material containing one or more of
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34668192A JP2771413B2 (en) | 1992-12-25 | 1992-12-25 | Phenolic resin molding material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34668192A JP2771413B2 (en) | 1992-12-25 | 1992-12-25 | Phenolic resin molding material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06192544A true JPH06192544A (en) | 1994-07-12 |
| JP2771413B2 JP2771413B2 (en) | 1998-07-02 |
Family
ID=18385100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP34668192A Expired - Lifetime JP2771413B2 (en) | 1992-12-25 | 1992-12-25 | Phenolic resin molding material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2771413B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011068705A (en) * | 2009-09-24 | 2011-04-07 | Sumitomo Bakelite Co Ltd | Phenolic resin molding material |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3407756B2 (en) | 1993-07-21 | 2003-05-19 | 住友ベークライト株式会社 | Phenolic resin molding materials |
-
1992
- 1992-12-25 JP JP34668192A patent/JP2771413B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011068705A (en) * | 2009-09-24 | 2011-04-07 | Sumitomo Bakelite Co Ltd | Phenolic resin molding material |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2771413B2 (en) | 1998-07-02 |
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