JPH1053692A - Phenolic resin molding material - Google Patents

Phenolic resin molding material

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Publication number
JPH1053692A
JPH1053692A JP21034396A JP21034396A JPH1053692A JP H1053692 A JPH1053692 A JP H1053692A JP 21034396 A JP21034396 A JP 21034396A JP 21034396 A JP21034396 A JP 21034396A JP H1053692 A JPH1053692 A JP H1053692A
Authority
JP
Japan
Prior art keywords
molding material
resin
amount
weight
phenolic resin
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
JP21034396A
Other languages
Japanese (ja)
Inventor
Shinichi Nakao
伸一 中尾
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 JP21034396A priority Critical patent/JPH1053692A/en
Publication of JPH1053692A publication Critical patent/JPH1053692A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a pheniolic resin molding material affording excellent mechanical strength, wear resistance and dimensional stability, and capable of suppressing its swelling due to moisture or oil absorption, blended with glass fibers, an organic natural material, fine silica particles and a lubricant thermoplastic resin in specified proportions. SOLUTION: This phenolic resin molding material contains 60-70wt.% of a total of (A) glass fibers, (B) an organic natural material (e.g. deseggregated pulp, raw pulp, powdered pulp, ground cloth, each <=0.1mm in fiber length), (C) fine silica particles (e.g. synthetic noncrystalline silica <=20μm in secondary agglomerated particle size), and (D) a lubricant thermoplastic resin (e.g. polyolefin resin, fluororesin). In this case, the respective proportions of the components A to D, based on the total amount of these components, are 75-93wt.%, 1-5wt.%, 5-15wt.%, and 1-5wt.%, respectively. It is preferably that 100 pts.wt. of this molding material contains 20-35 pts.wt. of phenolic resins containing 5-20 pts.wt. of a xylene-molding novolak-type pheniolic resin.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、強度、耐摩耗性に
優れ且つ、吸油・吸水等による膨潤が小さく、寸法安定
性に優れるフェノール樹脂成形材料に関するものであ
り、樹脂製プーリ、歯車等の機構部品に好適に使用され
得るものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a phenol resin molding material which is excellent in strength and wear resistance, has small swelling due to oil absorption and water absorption, and has excellent dimensional stability. It can be suitably used for mechanical parts.

【0002】[0002]

【従来の技術】近年自動車、電機部品をはじめとする構
造・機構部品の小型化、軽量化及び高性能化要求に従
い、強度、耐熱性、寸法安定性、応力緩和特性等に優れ
るガラス繊維充填フェノール樹脂成形材料が金属代替材
料として注目を集めている。しかし、ガラス繊維は強
度、耐熱性の向上には優れた効果が得られるが、その添
加量に反比例して摩耗特性は低下する。
2. Description of the Related Art In recent years, glass fiber-filled phenols having excellent strength, heat resistance, dimensional stability, stress relaxation properties, etc. in accordance with the demand for miniaturization, weight reduction and high performance of structural and mechanical parts such as automobiles and electric parts. Resin molding materials are attracting attention as metal substitute materials. However, glass fibers have an excellent effect on improving strength and heat resistance, but wear properties decrease in inverse proportion to the amount of glass fiber added.

【0003】一方、従来より、パルプ、粉砕布等の有機
天然繊維を配合すると摩耗特性が向上することが知られ
ているが、その反面ガラス繊維添加フェノール樹脂成形
材料の特長である耐熱性、強度等の低下は避けられなか
った。そこで、充填材として、有機天然繊維、シリカ粉
末、及び熱可塑性樹脂を配合することにより、耐熱性、
強度を損なわずに摩耗特性を向上できることが見いださ
れた(特開昭60−124646号公報、特願平4−2
14199号公報)が、更なる向上が望まれていた。
[0003] On the other hand, it has been conventionally known that the blending of organic natural fibers such as pulp and crushed cloth improves wear characteristics. On the other hand, heat resistance and strength, which are the characteristics of phenolic resin molding materials added with glass fibers, are known. Etc. were inevitable. Therefore, by blending organic natural fibers, silica powder, and thermoplastic resin as a filler, heat resistance,
It has been found that the wear characteristics can be improved without impairing the strength (Japanese Unexamined Patent Publication No. Sho 60-124646, Japanese Patent Application No. Hei 4-2).
No. 14199), but further improvement has been desired.

【0004】一方、ガラス繊維充填のフェノール樹脂成
形材料は寸法安定性に優れているが、高温中、高湿中、
あるいは水や油への浸漬中で長時間放置された場合、寸
法変化があるため、金属並みの精密な寸法精度が要求さ
れる部位への適用には限界があった。
On the other hand, a phenolic resin molding material filled with glass fiber has excellent dimensional stability,
Or, if left for a long time while immersed in water or oil, there is a dimensional change, so there is a limit to its application to a part that requires precise dimensional accuracy comparable to metal.

【0005】[0005]

【発明が解決しようとする課題】本発明に従えば、ガラ
ス繊維を高充填したフェノール樹脂成形材料の優れた機
械的強度を損なうことなく、摩耗特性に優れ、吸湿・吸
油等による膨潤が少なく、寸法安定性に優れたフェノー
ル樹脂成形材料が容易に得られる。また、得られたフェ
ノール樹脂成形材料は樹脂製プーリ、歯車等の機構部品
に好適に使用することができる。
According to the present invention, a phenolic resin molding material highly filled with glass fibers has excellent abrasion characteristics without impairing the excellent mechanical strength, and has little swelling due to moisture absorption and oil absorption. A phenolic resin molding material having excellent dimensional stability can be easily obtained. Further, the obtained phenol resin molding material can be suitably used for mechanical parts such as resin pulleys and gears.

【0006】[0006]

【課題を解決するための手段】本発明は、ガラス繊維、
有機天然材料、微粒子シリカ及び潤滑性熱可塑性樹脂が
成形材料全量に対し60〜70重量%含有され、前記4
種の各成分がこれら4成分の合計量に対してそれぞれ7
5〜93/1〜5/5〜15/1〜5重量%となるよう
に配合されてなることを特徴とするフェノール樹脂成形
材料、であり、好ましくは、フェノール樹脂が成形材料
全体に対して20〜35重量部配合され、そのフェノー
ル樹脂のうちのキシレン変性ノボラック樹脂が成形材料
全体に対して5〜20重量部配合されていて、さらに
は、前記微粒子シリカとして、2次凝集粒子径20μm
以下の合成非晶質シリカを用い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。
SUMMARY OF THE INVENTION The present invention provides a glass fiber,
The organic natural material, the fine particle silica and the lubricating thermoplastic resin are contained in an amount of 60 to 70% by weight based on the total amount of the molding material.
Each component of the species is 7
A phenolic resin molding material characterized by being blended so as to be 5 to 93/1 to 5/5 to 15/1 to 5% by weight. 20 to 35 parts by weight, of which the xylene-modified novolak resin of the phenolic resin is compounded in an amount of 5 to 20 parts by weight based on the whole molding material, and further, as the fine particle silica, a secondary aggregated particle diameter of 20 μm
The present invention relates to a phenol resin molding material characterized by using the following synthetic amorphous silica.

【0007】次にフェノール樹脂について説明する。本
発明に使用するキシレン変性フェノール樹脂は、通常の
ホルマリンとフェノールモノマーとの反応で得られるフ
ェノール樹脂に比べ親水性のあるフェノール性水酸基が
少ないため、耐水、耐湿特性が優れているが、その反
面、通常のフェノール樹脂に比べ硬化性に劣るため、単
独での使用には不適当である。そこで本発明ではキシレ
ン変性ノボラック樹脂と通常のフェノール樹脂を併用す
ることにより耐熱及び耐湿寸法安定性を損なうことな
く、成形材料用の組成物として使用するのに十分な硬化
性を得ている。
Next, the phenol resin will be described. The xylene-modified phenolic resin used in the present invention has less water-soluble and moisture-resistant properties because it has less hydrophilic phenolic hydroxyl groups than the phenolic resin obtained by the reaction of ordinary formalin and phenolic monomer, but on the other hand However, they are inferior in curability to ordinary phenolic resins and are therefore unsuitable for use alone. Thus, in the present invention, by using a xylene-modified novolak resin and a normal phenol resin in combination, sufficient curability for use as a composition for a molding material is obtained without impairing the dimensional stability of heat and humidity.

【0008】本発明において、フェノール樹脂成分の配
合量は、成形材料全体100重量部に対し20〜35重
量部であって、一般の成形材料より若干少な目に配合す
ることが望ましい。20重量部未満では成形材料化が困
難となることがあり、35重量部を越えると寸法変化が
大きくなる傾向があるからである。その内キシレン変性
ノボラック樹脂の配合量は5〜15重量部であることが
好ましい。5重量部未満では寸法安定性向上の効果が小
さく、15重量部を越えると硬化性が低下するからであ
る。また、同様の理由によりキシレン変性ノボラック樹
脂のキシレン変性率は20〜80重量部であることが好
ましい。
In the present invention, the compounding amount of the phenolic resin component is 20 to 35 parts by weight based on 100 parts by weight of the whole molding material, and it is desirable to mix the phenolic resin component in a slightly smaller amount than a general molding material. If the amount is less than 20 parts by weight, it may be difficult to form a molding material, and if it exceeds 35 parts by weight, the dimensional change tends to increase. The amount of the xylene-modified novolak resin is preferably 5 to 15 parts by weight. If the amount is less than 5 parts by weight, the effect of improving the dimensional stability is small, and if it exceeds 15 parts by weight, the curability decreases. For the same reason, the xylene-modified novolak resin preferably has a xylene modification ratio of 20 to 80 parts by weight.

【0009】他のフェノール樹脂成分として通常のノボ
ラック樹脂を5〜20重量部用いる。5重量部未満では
硬化性の向上が小さく、20重量部を越えると耐湿性が
低下する。また、本発明では、特に限定するものではな
いが、寸法安定性付与のために10重量部以下の量でレ
ゾール樹脂を併用してもよい。10重量部以上配合する
と硬化性が低下するからである。
As the other phenol resin component, 5 to 20 parts by weight of a normal novolak resin is used. If the amount is less than 5 parts by weight, the improvement in curability is small, and if it exceeds 20 parts by weight, the moisture resistance decreases. In the present invention, although not particularly limited, a resol resin may be used in an amount of 10 parts by weight or less for imparting dimensional stability. This is because if more than 10 parts by weight is added, the curability is reduced.

【0010】フェノール樹脂を硬化させるために、硬化
剤として通常ヘキサメチレンテトラミンを使用する。ヘ
キサメチレンテトラミンの量は、通常使用されている量
であり、ノボラック樹脂の対して15〜20重量%であ
る。
To cure the phenolic resin, hexamethylenetetramine is usually used as a curing agent. The amount of hexamethylenetetramine is a commonly used amount and is 15 to 20% by weight based on the novolak resin.

【0011】次に充填材について説明する。本発明にお
いては、充填材として、ガラス繊維、有機天然材料、微
粒子シリカ及び潤滑性熱可塑性樹脂の4種を必須成分と
して使用する。ガラス繊維は、通常成形材料に用いられ
ているチョップドストランドであれば如何なるものでも
よいが、成形材料化した際の均一に分散するためには1
〜6mmの繊維長のものが好ましい。ガラス繊維の配合
量は前記4成分中75〜93重量%である。この範囲よ
り多いと耐磨耗性が低下し、少ないと強度なと機械的特
性において不十分となることがある。
Next, the filler will be described. In the present invention, as a filler, four kinds of glass fiber, organic natural material, fine particle silica and lubricating thermoplastic resin are used as essential components. The glass fiber is not particularly limited as long as it is a chopped strand that is usually used for a molding material.
Fiber lengths of 66 mm are preferred. The blending amount of the glass fiber is 75 to 93% by weight in the above four components. If the amount is more than this range, the abrasion resistance decreases, and if the amount is less than this, the mechanical properties may be insufficient if the strength is high.

【0012】有機天然材料としては、解綿パルプ、原綿
パルプ、粉末パルプ、粉砕布、木粉、モミガラ粉、合板
粉等種々のものを使用することができるが、成形材料化
した際の解繊度、分散度、成形材料のかさばり等によ
り、解綿パルプ、原綿パルプ、粉末パルプ、粉砕布等の
繊維状物が好ましく、特に繊維長1mm以下の細かいも
のが望ましい。有機天然材料の配合量は、寸法安定性を
損ねない様、充填材全体に対し5重量%以下が好まし
い。また1重量%未満では、配合効果が不十分である。
本発明においては、有機天然材料と併用したとき耐摩耗
性向上に効果のある微粒子シリカを使用する。微粒子シ
リカは粒子径20μm以下のものが好ましく、更に好ま
しくは2次凝集粒子径が20μm以下の合成非晶質シリ
カを用いる。2次凝集粒子径が20μm以上では、成形
材料中での均一分散性が低下するし、成形時の金型・シ
リンダー等の摩耗が大きくなる。ここでいう合成非晶質
シリカとは、粒子径50nm以下の単粒子が葡萄の房状
に2次凝集した構造をしており、成形材料化時に再び単
粒子化するため、均一分散性に優れているものである。
配合量は、充填材全体に対し15重量%以下が好まし
い。また5重量%未満では、配合効果が十分現れない。
As the organic natural material, various types such as defibrated pulp, raw cotton pulp, powdered pulp, crushed cloth, wood powder, fir powder, and plywood powder can be used. Fibrous materials such as defibrated pulp, raw cotton pulp, powder pulp, and crushed cloth are preferred depending on the degree of dispersion, the bulk of the molding material, and the like, and particularly preferred are fine fibers having a fiber length of 1 mm or less. The amount of the organic natural material is preferably 5% by weight or less based on the whole filler so as not to impair the dimensional stability. If it is less than 1% by weight, the compounding effect is insufficient.
In the present invention, fine particle silica which is effective in improving abrasion resistance when used in combination with an organic natural material is used. The fine particle silica preferably has a particle diameter of 20 μm or less, and more preferably a synthetic amorphous silica having a secondary aggregated particle diameter of 20 μm or less. When the secondary aggregated particle diameter is 20 μm or more, the uniform dispersibility in the molding material is reduced, and the abrasion of a mold, a cylinder, and the like during molding is increased. The term “synthetic amorphous silica” as used herein refers to a structure in which single particles having a particle diameter of 50 nm or less are secondary aggregated in a bunch of grapes. Is what it is.
The amount is preferably 15% by weight or less based on the whole filler. If it is less than 5% by weight, the compounding effect is not sufficiently exhibited.

【0013】さらには、成形品表面に皮膜を形成し摩耗
係数を低下させる働きがある潤滑性熱可塑性樹脂を少量
用いる。その具体例としては、ポリエチレン等のポリオ
レフィン、四フッ化エチレン樹脂などのフッ素樹脂等が
好ましく使用できる。いずれも融点、分子量等は特に限
定されないが、フェノール樹脂との相溶性、分散性、材
料化の際の作業性を損なわない程度の特性のものが効果
的に使用される。例えばポリエチレン樹脂は融点120
℃以下、粒径50μm以下、四フッ化エチレン樹脂は融
点400℃以下、粒径50μm以下のものがこれにあて
はまる。配合量は、前記4成分に対して5重量%以下が
望ましく、それより多いと滑りすぎて成形材料化が困難
となるし、材料コストも増大するからである。また1重
量%未満ではその配合効果が十分に現れない。
Further, a small amount of a lubricating thermoplastic resin having a function of forming a film on the surface of the molded article and reducing the wear coefficient is used. Specific examples thereof include polyolefins such as polyethylene, and fluororesins such as tetrafluoroethylene resin. In any case, the melting point, molecular weight, and the like are not particularly limited, but those having properties such that compatibility with the phenol resin, dispersibility, and workability during materialization are not impaired are effectively used. For example, polyethylene resin has a melting point of 120.
C. or less, particle size of 50 .mu.m or less, and the melting point of the tetrafluoroethylene resin is 400.degree. C. or less, and the particle size is 50 .mu.m or less. The blending amount is desirably 5% by weight or less based on the above-mentioned four components. If the amount is more than 5%, slippage is excessive, making it difficult to form a molding material and increasing the material cost. If the amount is less than 1% by weight, the effect of the compounding is not sufficiently exhibited.

【0014】本発明におけるフェノール樹脂成形材料
は、必要により上記以外の充填材を配合してもよく、こ
れらの他に、硬化助剤、離型剤、顔料等を配合すること
も可能である。成形材料を製造するには、これらの各成
分を熱ロール等により混練し、粉砕して得られる。
The phenolic resin molding material of the present invention may optionally contain a filler other than those described above, and may further contain a curing aid, a release agent, a pigment and the like. In order to produce a molding material, these components are kneaded with a hot roll or the like, and then pulverized.

【0015】[0015]

【実施例】以下、本発明の実施例を示す。実施例及び比
較例の配合を表1に、得られた特性を表2にそれぞれ示
す。
Embodiments of the present invention will be described below. Table 1 shows the compositions of Examples and Comparative Examples, and Table 2 shows the properties obtained.

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【表2】 [Table 2]

【0018】《測定方法》 ・摺動摩耗鈴木式摩耗試験機を用いて測定した。(荷重
2kgf/cm2 、滑り速度 1000mm/sec、試験時間1時
間) ・たたき摩耗量は住友ベークライト製たたき摩耗測定機
を用いて測定した。(接触面積16mm2 、荷重12.5k
gf/cm2 、たたき回数 150,000回) ・寸法変化は50φ×3mm成形品の径方向の寸法変化
率を測定した。 ・他の特性は JIS K 6911 に準じて測定した。 表2の結果より明らかなように、いずれの実施例も強度
及び耐熱性を低下させずに摩耗特性及び寸法安定性を向
上させ留ことができる。比較例1は無機充填材としてガ
ラス繊維のみを用いた例である。実施例と比べ強度に優
れるが、摩耗特性に劣る。比較例2は粉砕布を多量に配
合した例である。摩耗特性が良好な反面、強度・耐熱性
・寸法安定性いずれも著しく低下している。比較例3は
通常のフェノール樹脂のみを用いた例であるが、寸法安
定性に劣る。
<< Measurement Method >> Sliding wear: Measured using a Suzuki abrasion tester. (Load: 2 kgf / cm 2 , Sliding speed: 1000 mm / sec, Test time: 1 hour)-The amount of tapping wear was measured using a tapping wear measuring device manufactured by Sumitomo Bakelite. (Contact area 16mm 2 , load 12.5k
(gf / cm 2 , number of taps: 150,000 times) ・ Dimensional change was measured by measuring the rate of dimensional change in the radial direction of a 50 mm × 3 mm molded product. -Other characteristics were measured according to JIS K6911. As is clear from the results in Table 2, any of the examples can improve the wear characteristics and the dimensional stability without lowering the strength and the heat resistance, and can be retained. Comparative Example 1 is an example using only glass fiber as the inorganic filler. It is superior in strength to the example, but is inferior in wear characteristics. Comparative Example 2 is an example in which pulverized cloth was blended in a large amount. While the wear characteristics are good, all of the strength, heat resistance and dimensional stability are remarkably reduced. Comparative Example 3 is an example using only a normal phenol resin, but is inferior in dimensional stability.

【0019】[0019]

【発明の効果】実施例及び比較例より明らかなように、
本発明のフェノール樹脂成形材料は、ガラス繊維充填フ
ェノール樹脂成形材料の特長である高強度、耐熱性等の
特性はもちろんのこと、有機天然材料と微粒子シリカの
併用及び潤滑性熱可塑性樹脂の配合により優れた摩耗特
性を有し、且つキシレン変性レジンの併用により吸油・
吸水による寸法変化が小さいという特長を示す。このよ
うな特性を有することから、本発明のフェノール樹脂成
形材料は樹脂製プーリや歯車等の機構部品に好適に使用
される。
As is clear from the examples and comparative examples,
The phenolic resin molding material of the present invention is not only characterized by high strength and heat resistance, which are the characteristics of the glass fiber-filled phenolic resin molding material, but also by the combined use of organic natural materials and fine particle silica and the blending of a lubricating thermoplastic resin. It has excellent wear characteristics, and has an oil absorption and
It has the advantage of small dimensional change due to water absorption. Because of having such characteristics, the phenolic resin molding material of the present invention is suitably used for mechanical parts such as resin pulleys and gears.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ガラス繊維、有機天然材料、微粒子シリ
カ及び潤滑性熱可塑性樹脂が成形材料全量に対し60〜
70重量%含有され、前記4種の各成分がこれら4成分
の合計量に対してそれぞれ75〜93/1〜5/5〜1
5/1〜5重量%となるように配合されてなることを特
徴とするフェノール樹脂成形材料。
1. The glass fiber, the organic natural material, the finely divided silica and the lubricating thermoplastic resin are used in an amount of 60 to 100% based on the total amount of the molding material.
70% by weight, and each of the four components is 75 to 93/1 to 5/5 to 1 with respect to the total amount of these four components.
A phenolic resin molding material characterized by being blended so as to be 5/1 to 5% by weight.
【請求項2】 フェノール樹脂が成形材料全体に対して
20〜35重量部配合され、そのフェノール樹脂のうち
のキシレン変性ノボラック樹脂が成形材料全体に対して
5〜15重量部配合されている請求項1記載のフェノー
ル樹脂成形材料。
2. A phenol resin is blended in an amount of 20 to 35 parts by weight based on the whole molding material, and a xylene-modified novolak resin of the phenol resin is incorporated in an amount of 5 to 15 parts by weight based on the entire molding material. 2. The phenolic resin molding material according to 1.
【請求項3】 微粒子シリカとして、2次凝集粒子径2
0μm以下の合成非晶質シリカを用いる請求項1又は2
記載のフェノール樹脂成形材料。
3. A secondary aggregated particle diameter of 2 as fine particle silica
3. A synthetic amorphous silica having a particle size of 0 [mu] m or less.
The phenolic resin molding material according to the above.
JP21034396A 1996-08-08 1996-08-08 Phenolic resin molding material Pending JPH1053692A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21034396A JPH1053692A (en) 1996-08-08 1996-08-08 Phenolic resin molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21034396A JPH1053692A (en) 1996-08-08 1996-08-08 Phenolic resin molding material

Publications (1)

Publication Number Publication Date
JPH1053692A true JPH1053692A (en) 1998-02-24

Family

ID=16587840

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21034396A Pending JPH1053692A (en) 1996-08-08 1996-08-08 Phenolic resin molding material

Country Status (1)

Country Link
JP (1) JPH1053692A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004042146A (en) * 2002-07-08 2004-02-12 Fudow Co Ltd Tool holder holding tool constitutive material, and tool holder holding tool
JP2006265320A (en) * 2005-03-23 2006-10-05 Sumitomo Bakelite Co Ltd Phenolic resin molding material
US7452926B2 (en) * 2002-08-29 2008-11-18 Jtekt Corporation Resin pulley formed of a resin composition having a phenol resin, an inorganic powder , a reinforcing fiber, and a lubricant
US7772317B2 (en) 2005-11-11 2010-08-10 Hitachi Chemical Company, Ltd. Resin molding material
JP2011068705A (en) * 2009-09-24 2011-04-07 Sumitomo Bakelite Co Ltd Phenolic resin molding material
JP2011089095A (en) * 2009-10-26 2011-05-06 Panasonic Electric Works Co Ltd Phenolic resin molding material and phenolic resin molded article
WO2011108326A1 (en) * 2010-03-01 2011-09-09 出光興産株式会社 Surface-coated metal plate and metal treatment method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004042146A (en) * 2002-07-08 2004-02-12 Fudow Co Ltd Tool holder holding tool constitutive material, and tool holder holding tool
US7452926B2 (en) * 2002-08-29 2008-11-18 Jtekt Corporation Resin pulley formed of a resin composition having a phenol resin, an inorganic powder , a reinforcing fiber, and a lubricant
JP2006265320A (en) * 2005-03-23 2006-10-05 Sumitomo Bakelite Co Ltd Phenolic resin molding material
US7772317B2 (en) 2005-11-11 2010-08-10 Hitachi Chemical Company, Ltd. Resin molding material
JP2011068705A (en) * 2009-09-24 2011-04-07 Sumitomo Bakelite Co Ltd Phenolic resin molding material
JP2011089095A (en) * 2009-10-26 2011-05-06 Panasonic Electric Works Co Ltd Phenolic resin molding material and phenolic resin molded article
WO2011108326A1 (en) * 2010-03-01 2011-09-09 出光興産株式会社 Surface-coated metal plate and metal treatment method
JP2011179066A (en) * 2010-03-01 2011-09-15 Idemitsu Kosan Co Ltd Surface-coated metal sheet and metal working method

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