JP2001181044A - Carbonaceous sliding material and method for producing the same - Google Patents

Carbonaceous sliding material and method for producing the same

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Publication number
JP2001181044A
JP2001181044A JP2000147490A JP2000147490A JP2001181044A JP 2001181044 A JP2001181044 A JP 2001181044A JP 2000147490 A JP2000147490 A JP 2000147490A JP 2000147490 A JP2000147490 A JP 2000147490A JP 2001181044 A JP2001181044 A JP 2001181044A
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JP
Japan
Prior art keywords
carbon
sliding
sliding material
mixture
cluster diamond
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
Application number
JP2000147490A
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Japanese (ja)
Other versions
JP4753455B2 (en
Inventor
Yoshihisa Suda
吉久 須田
Seiichiro Hironaka
清一郎 広中
Yasushi Yamamoto
泰 山本
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.)
Mitsubishi Pencil Co Ltd
Original Assignee
Mitsubishi Pencil Co Ltd
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Priority to JP2000147490A priority Critical patent/JP4753455B2/en
Publication of JP2001181044A publication Critical patent/JP2001181044A/en
Application granted granted Critical
Publication of JP4753455B2 publication Critical patent/JP4753455B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Sliding-Contact Bearings (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a carbonaceous composite sliding material excellent in sliding characteristics and mechanical strength and formable into an optional and complicated shape. SOLUTION: This carbonaceous sliding material comprising a composite of a cluster diamond and amorphous carbon is obtained by mixing a starting raw material of the amorphous carbon with a cluster diamond powder, shaping the resultant mixture into an optional form and then baking the shaped mixture.

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、炭素系摺動材料及
びその製造方法に関するものである。
TECHNICAL FIELD The present invention relates to a carbon-based sliding material and a method for producing the same.

【0002】[0002]

【従来の技術】炭素からなる摺動材料は、耐熱性、耐薬
品性に優れ、しかも軽量であるという優れた利点を持っ
ており、従来の金属系、および高分子系の摺動材料が使
用できない高温や腐食性などの雰囲気下で使用されてい
る。従来の炭素からなる摺動材料は主にガラス状炭素か
らなる材料と黒鉛質の等方性炭素からなる材料とに分類
される。ガラス状炭素からなる摺動材は摩擦係数が低
く、比摩耗量が小さいといった優れた摺動特性を示す
が、高硬度で耐機械衝撃性が弱いために、加工性が劣
る。一方、黒鉛質の等方性炭素からなる摺動材は自己潤
滑性を有するが、機械的強度が劣る。
2. Description of the Related Art A sliding material made of carbon has an excellent advantage of being excellent in heat resistance, chemical resistance, and light weight. Conventional metallic and polymer sliding materials are used. It is used in an environment where high temperatures and corrosiveness are not possible. Conventional carbon sliding materials are mainly classified into glassy carbon materials and graphitic isotropic carbon materials. A sliding material made of glassy carbon exhibits excellent sliding characteristics such as a low coefficient of friction and a small specific wear, but is inferior in workability due to its high hardness and poor mechanical impact resistance. On the other hand, a sliding material made of graphite-like isotropic carbon has self-lubricating properties, but has poor mechanical strength.

【0003】さらに、ガラス状炭素や等方性炭素材など
の従来の炭素からなる摺動材料では、特に、機械的強度
や剛性の劣る炭素材の欠点を緩和するために設定されて
いる低速度低荷重条件下において十分な摺動特性を得る
ことができていない。またこれら従来の炭素からなる摺
動材は板形状体やブロック形状体から切削加工により作
成するために無駄になる材料の量が多く、煩雑な製造工
程を経るため、コストが高くなる欠点を有している。そ
の上任意且つ複雑な形状体を得ることが困難であった。
Further, in conventional sliding materials made of carbon such as glassy carbon and isotropic carbon material, low speed materials set in order to alleviate defects of carbon materials having poor mechanical strength and rigidity are particularly used. Sufficient sliding characteristics have not been obtained under low load conditions. In addition, these conventional sliding members made of carbon have the disadvantage that a large amount of material is wasted because they are made by cutting from a plate-shaped body or a block-shaped body, and the manufacturing process goes through a complicated manufacturing process, which increases the cost. are doing. Moreover, it was difficult to obtain an arbitrary and complicated shape.

【0004】[0004]

【発明が解決しようとする課題】本発明はかかる問題点
に鑑みてなされたもので、その第1の目的は従来の炭素
からなる材料よりも良好な自己潤滑性を有し、摩擦係数
が低く比摩耗量が小さいといった摺動特性に優れ、耐機
械衝撃性、機械的強度に優れ、任意且つ複雑な形状に成
形が可能な炭素系摺動材料を簡便な工程で安価に提供す
ることにある。
SUMMARY OF THE INVENTION The present invention has been made in view of the above problems, and a first object of the present invention is to have better self-lubricating properties and a lower coefficient of friction than conventional carbon materials. An object of the present invention is to provide a carbon-based sliding material that is excellent in sliding characteristics such as a small specific wear amount, excellent in mechanical shock resistance and mechanical strength, and can be formed into an arbitrary and complicated shape at a simple process at a low cost. .

【0005】本発明の第2の目的は、従来の炭素からな
る材料よりも、特に低速度低荷重条件下における摩擦係
数が低く比摩耗量が小さいといった摺動特性に優れた炭
素系摺動材料を簡便な工程で安価に提供することにあ
る。
A second object of the present invention is to provide a carbon-based sliding material which is superior to conventional carbon-based materials in terms of sliding characteristics such as a low coefficient of friction and a small specific wear under low-speed and low-load conditions. In a simple process at a low cost.

【0006】[0006]

【課題を解決するための手段】発明者らは、このような
実状に鑑み、鋭意研究の結果、アモルファス炭素の出発
原料に、炭素粉末を混合し、必要とされる形状に賦形
後、焼成することにより得られた炭素粉末とアモルファ
ス炭素を含む炭素系摺動材料は、優れた摺動特性、耐機
械衝撃性を有する上、より簡便な工程で製造しうること
など前記課題が効果的に解決しうる事実を確認した。
Means for Solving the Problems In view of such circumstances, the present inventors have conducted intensive studies and as a result, mixed carbon powder with the starting material of amorphous carbon, formed the mixture into a required shape, and then fired. The carbon-based sliding material containing carbon powder and amorphous carbon obtained by doing the above, has excellent sliding properties, mechanical shock resistance, and the above-described problem such as being able to be manufactured in a simpler process is effectively achieved. Confirmed the fact that can be solved.

【0007】またさらに、前記炭素粉末として、クラス
ターダイヤモンド含むものを使用すれば、特に低速度低
荷重条件下で優れた摺動特性を有することが判明した。
このクラスターダイヤモンドは、摺動材料中に5質量%
以上含まれていることが好ましい。アモルファス炭素の
出発原料としては、好ましくは不活性ガス雰囲気中での
焼成により5%以上の炭化収率を示す有機物質が使用さ
れる。具体的には、ポリ塩化ビニル、ポリアクリロニト
リル、ポリビニルアルコール、ポリ塩化ビニル−ポリ酢
酸ビニル共重合体、ポリアミド等の熱可塑性樹脂、フェ
ノール樹脂、フラン樹脂、イミド樹脂、エポキシ樹脂、
不飽和ポリエステル樹脂等の熱硬化性樹脂、リグニン、
セルロース、トラカントガム、アラビアガム、糖類等の
縮合多環芳香族を分子の基本構造内にもつ天然高分子物
質、および前記には包含されない、ナフタレンスルホン
酸のホルマリン縮合物、コプナ樹脂等の縮合多環芳香族
を分子の基本構造内にもつ合成高分子物質が挙げられ
る。使用する組成物の種類と量は、目的とする摺動材料
の特性、強度、形状により適宜選択され、単独でも2種
以上の混合体でも使用することができるが、特にフラン
樹脂、フェノール樹脂、イミド樹脂等の熱硬化性樹脂を
使用することが好ましく、摺動材料としての必要な特性
と形状を賦与するためにもその使用量は30重量部以上
が好ましい。
Further, it has been found that the use of a carbon powder containing a cluster diamond as the carbon powder has excellent sliding characteristics, particularly under low speed and low load conditions.
This cluster diamond is 5% by mass in the sliding material.
It is preferable that the above is included. As a starting material for the amorphous carbon, an organic substance is preferably used which shows a carbonization yield of 5% or more by firing in an inert gas atmosphere. Specifically, polyvinyl chloride, polyacrylonitrile, polyvinyl alcohol, polyvinyl chloride-polyvinyl acetate copolymer, thermoplastic resin such as polyamide, phenol resin, furan resin, imide resin, epoxy resin,
Thermosetting resin such as unsaturated polyester resin, lignin,
Cellulose, tracant gum, gum arabic, condensed polycyclic aromatic substances such as saccharides and the like in the basic structure of the molecule and natural polymer substances which are not included in the above, formalin condensates of naphthalenesulfonic acid, condensed polycyclics such as copna resin Synthetic high-molecular substances having aromatics in the basic structure of the molecule can be mentioned. The type and amount of the composition to be used are appropriately selected depending on the properties, strength, and shape of the intended sliding material, and can be used alone or in a mixture of two or more. Particularly, a furan resin, a phenol resin, It is preferable to use a thermosetting resin such as an imide resin, and the amount used is preferably 30 parts by weight or more in order to impart necessary characteristics and shape as a sliding material.

【0008】前述の炭素粉末としては、黒鉛、ダイヤモ
ンド、グラファイトクラスターダイヤモンド、クラスタ
ーダイヤモンド、フラーレンおよびカーボンブラック等
があり、使用する炭素粉末の種類と量も目的とする摺動
材料の特性、強度、形状により適宜選択され、単独でも
2種以上の混合体でも使用することができるが、前述し
たように特に低速度低荷重条件下での摺動特性を高める
観点からクラスターダイヤモンドを含むものを使用する
ことが好ましい。
The above-mentioned carbon powder includes graphite, diamond, graphite cluster diamond, cluster diamond, fullerene, carbon black, and the like. The type and amount of the carbon powder used also depends on the characteristics, strength and shape of the intended sliding material. Can be used singly or as a mixture of two or more, but as described above, a material containing cluster diamond should be used from the viewpoint of enhancing the sliding characteristics particularly under low speed and low load conditions. Is preferred.

【0009】本発明において、さらに好ましくは、アモ
ルファス炭素の出発原料として、不活性ガス雰囲気中で
の焼成により5%以上の炭化収率を示し機械的強度特性
の優れる有機物質が使用される。具体的には、フェノー
ル樹脂、フラン樹脂、イミド樹脂、エポキシ樹脂、不飽
和ポリエステル樹脂等の熱硬化性樹脂やナフタレンスル
ホン酸のホルマリン縮合物、コプナ樹脂等の縮合多環芳
香族を分子の基本構造内にもつ合成高分子物質が挙げら
れる。使用する組成物の種類と量は、目的とする摺動材
料の特性、強度、形状により適宜選択され、単独でも2
種以上の混合体でも使用することができるが、製造の簡
便さから常温で液状を示すフラン樹脂やフェノール樹脂
を使用することが好ましい。
In the present invention, more preferably, as a starting material of the amorphous carbon, an organic substance having a carbonization yield of 5% or more by firing in an inert gas atmosphere and having excellent mechanical strength characteristics is used. Specifically, a thermosetting resin such as a phenol resin, a furan resin, an imide resin, an epoxy resin, and an unsaturated polyester resin; a formalin condensate of naphthalenesulfonic acid; and a condensed polycyclic aromatic compound such as a copna resin have a basic structure of a molecule. And synthetic high molecular substances contained therein. The type and amount of the composition used are appropriately selected depending on the properties, strength and shape of the intended sliding material.
Although a mixture of more than two kinds can be used, it is preferable to use a furan resin or a phenol resin which is liquid at normal temperature for ease of production.

【0010】前述の賦形方法には、圧縮成形、トランス
ファ成形、押し出し成形、射出成形、真空成形及び吹込
成形等の、一般的に普及している成形方法が挙げられ
る。前述の樹脂と炭素粉末(特に、クラスターダイヤモ
ンド粉末)の混合物の性状及び賦形形状により適宜選択
使用することが好ましい。以下に本発明による炭素系摺
動材料の製造方法を説明する。まず、樹脂組成物と炭素
粉末(クラスターダイヤモンド粉末)とを混合機を用い
てよく混合させる。得られた混合物を、混合物の性状、
賦形形状により選択した成型方法を用いて賦形する。次
に賦形体を炭素前駆体化処理し、得られた炭素前駆体を
窒素、アルゴン等の不活性ガス雰囲気中または真空雰囲
気下にて1000℃以上、好ましく2000℃程度まで
加熱昇温し、炭素(クラスターダイヤモンド)とアモル
ファス炭素とからなる炭素系摺動材料を得る。昇温速度
が大きいと賦形体の形状が変形したり微細なクラックが
発生する等の欠陥が生じるため昇温速度は500℃まで
は毎時100℃以下好ましくは毎時50℃以下が適切で
ある。
[0010] The above-mentioned shaping methods include commonly used molding methods such as compression molding, transfer molding, extrusion molding, injection molding, vacuum molding and blow molding. It is preferable to appropriately select and use the mixture according to the properties and the shape of the mixture of the resin and the carbon powder (particularly, cluster diamond powder). Hereinafter, a method for producing a carbon-based sliding material according to the present invention will be described. First, a resin composition and carbon powder (cluster diamond powder) are mixed well using a mixer. The resulting mixture, the properties of the mixture,
The shaping is performed using a molding method selected according to the shaping shape. Next, the shaped body is subjected to a carbon precursor treatment, and the obtained carbon precursor is heated and heated to 1000 ° C. or higher, preferably about 2000 ° C. in an inert gas atmosphere such as nitrogen or argon or in a vacuum atmosphere. (Cluster diamond) and a carbon-based sliding material comprising amorphous carbon are obtained. When the heating rate is high, defects such as deformation of the shape of the shaped body and generation of fine cracks occur. Therefore, the heating rate is preferably 100 ° C./hour or less, preferably 50 ° C./hour or less, up to 500 ° C.

【0011】[0011]

【実施例】以下に、実施例によって本発明をさらに具体
的に説明するが、本発明はこの実施例によって何等限定
されるものではない。 (実施例1)フラン樹脂(日立化成社製 ヒタフランV
F−303)90質量%にクラスターダイヤモンド(平
均一次粒子径 50Å)10質量%とを混合してポニー
ミキサーにて攬拌した後アプリケーターを用いてフィル
ム状に成形した。該フィルムを円盤状に切断し、これを
窒素雰囲気中の焼成炉で500℃までを25℃/時の昇
温速度で昇温し、その後1400℃までを100℃/時
で昇温し、1400℃で3時間保持した後自然冷却して
焼成を完了し、厚さ1.0mmの摺動特性試験片を得た。
得られた試験片を、ピン−円板型摩擦試験機を用いて、
該試験片とR0.5mmのアルミナのピンを組み合わせ、
すべり速度0.05〜1.5m/秒、荷重19.6N、
摺動時間22時間の条件下で摺動試験を実施した。更に
得られた試験片を長さ50mm、幅10mmの大きさに切断
し、圧縮試験機を用いて曲げ強度測定および弾性率測定
をするとともに40gの鉄球を落下させて試験片が破壊
される高さを測定した。
EXAMPLES The present invention will be described in more detail with reference to the following Examples, which should not be construed as limiting the present invention. (Example 1) Furan resin (Hitafuran V manufactured by Hitachi Chemical Co., Ltd.)
F-303) (90% by mass) was mixed with 10% by mass of cluster diamond (average primary particle size: 50 °), mixed with a pony mixer, and formed into a film using an applicator. The film is cut into a disc shape, and the film is heated in a firing furnace in a nitrogen atmosphere up to 500 ° C. at a rate of 25 ° C./hour, and then up to 1400 ° C. at 100 ° C./hour. After holding at 3 ° C. for 3 hours, the mixture was naturally cooled to complete firing, and a sliding property test piece having a thickness of 1.0 mm was obtained.
The obtained test piece, using a pin-disk friction tester,
Combine the test piece with an R0.5 mm alumina pin,
Sliding speed 0.05-1.5m / sec, load 19.6N,
A sliding test was performed under a sliding time of 22 hours. Further, the obtained test piece is cut into a size of 50 mm in length and 10 mm in width, and the bending strength and the elastic modulus are measured using a compression tester, and the test piece is broken by dropping a 40 g iron ball. The height was measured.

【0012】結果を表−1に示す。表−1によれば、特
に摩擦特性の優れたものが得られた。 (比較例1)フラン樹脂(日立化成社製 ヒタフランV
F−303)80質量%に天然黒鉛微粉末(日本黒鉛社
製 平均粒度5μm)20質量%を混合してポニーミキ
サーにて攬拌した後、押し出し成形機を用いてフィルム
状に成形した。該フィルムを真空成形機にて円盤状に賦
形した。これを耐熱セラミック板に挟み、真空焼成炉中
で500℃までを毎時25℃の昇温速度で昇温し、その
後1400℃までを毎時100℃で昇温し、1400℃
で3時間保持した後自然冷却して焼成を完了し、厚さ
1.0mmの摺動特性試験片を得た。得られた試験片につ
いて、実施例1と同様に摺動試験、耐衝撃性試験を実施
し、表−1に示す結果が得られた。 (比較例2)フラン樹脂(日立化成社製 ヒタフランV
F−303)80質量%にカーボンブラック(三菱化成
社製 一次粒子径5nm)20質量%を混合し、ヘンシェ
ルミキサーにて混合し、次いで120℃に加熱したロー
ルミキサーにて混練をおこなった。該混練物を圧縮成形
機を使用して円盤状に賦形した。窒素雰囲気中の焼成炉
で500℃までを毎時25℃の昇温速度で昇温し、その
後1400℃までを毎時100℃で昇温し、1400℃
で3時間保持した後自然冷却して焼成を完了し、厚さ
1.0mmの摺動特性試験片を得た。実施例1と同様に摺
動試験、曲げ強度試験、耐機械衝撃性試験を実施した。
結果を表−1に示す。 (比較例3)フラン樹脂(日立化成社製 ヒタフランV
F−303)を製膜機を用いてフィルム状に成形した。
該フィルムを円盤状に切断し、これを窒素雰囲気中の焼
成炉で500℃までを毎時25℃の昇温速度で昇温し、
その後1400℃までを毎時100℃で昇温し、140
0℃で3時間保持した後自然冷却して焼成を完了し、厚
さ1.0mmの摺動特性試験片を得た。実施例1と同様に
摺動試験、曲げ強度試験、耐機械衝撃性試験を実施し
た。結果を表−1に示す。 (比較例4)黒鉛質等方性炭素材料(東洋炭素社製)の
ブロックを円盤状に切削加工し、厚さ1.0mmの摺動特
性試験片を得た。実施例1と同様に摺動試験、曲げ強度
試験、耐機械衝撃性試験を実施した。結果を表−1に示
す。
The results are shown in Table 1. According to Table 1, particularly excellent frictional characteristics were obtained. (Comparative Example 1) Furan resin (Hitafuran V manufactured by Hitachi Chemical Co., Ltd.)
F-303) was mixed with 20% by mass of natural graphite fine powder (average particle size: 5 μm, manufactured by Nippon Graphite Co., Ltd.) in 80% by mass, stirred with a pony mixer, and formed into a film using an extruder. The film was shaped into a disk using a vacuum forming machine. This was sandwiched between heat-resistant ceramic plates, and the temperature was raised up to 500 ° C. at a rate of 25 ° C./hour in a vacuum firing furnace, and then raised to 1400 ° C. at 100 ° C./hour.
After holding for 3 hours, firing was completed by natural cooling to obtain a sliding property test piece having a thickness of 1.0 mm. A sliding test and an impact resistance test were performed on the obtained test piece in the same manner as in Example 1, and the results shown in Table 1 were obtained. (Comparative Example 2) Furan resin (Hitafuran V manufactured by Hitachi Chemical Co., Ltd.)
F-303) was mixed with 20% by mass of carbon black (primary particle size: 5 nm, manufactured by Mitsubishi Kasei Co., Ltd.) and mixed with a Henschel mixer, and then kneaded with a roll mixer heated to 120 ° C. The kneaded material was shaped into a disk using a compression molding machine. In a baking furnace in a nitrogen atmosphere, the temperature was raised up to 500 ° C. at a rate of 25 ° C./hour, and then up to 1400 ° C. at 100 ° C./hour, and 1400 ° C.
After holding for 3 hours, firing was completed by natural cooling to obtain a sliding property test piece having a thickness of 1.0 mm. A sliding test, a bending strength test, and a mechanical impact resistance test were performed in the same manner as in Example 1.
The results are shown in Table 1. (Comparative Example 3) Furan resin (Hitafuran V manufactured by Hitachi Chemical Co., Ltd.)
F-303) was formed into a film using a film-forming machine.
The film was cut into a disc shape, and this was heated in a firing furnace in a nitrogen atmosphere up to 500 ° C. at a rate of 25 ° C./hour,
Thereafter, the temperature was raised to 1400 ° C. at 100 ° C./hour,
After holding at 0 ° C. for 3 hours, the mixture was naturally cooled to complete firing, and a sliding property test piece having a thickness of 1.0 mm was obtained. A sliding test, a bending strength test, and a mechanical impact resistance test were performed in the same manner as in Example 1. The results are shown in Table 1. (Comparative Example 4) A block of a graphitic isotropic carbon material (manufactured by Toyo Tanso Co., Ltd.) was cut into a disc shape to obtain a sliding property test piece having a thickness of 1.0 mm. A sliding test, a bending strength test, and a mechanical impact resistance test were performed in the same manner as in Example 1. The results are shown in Table 1.

【0013】[0013]

【表1】 [Table 1]

【0014】(実施例2)硬質なアモルファス炭素源と
してのフラン樹脂(日立化成社製 ヒタフランVF−3
03)92質量%にクラスターダイヤモンド(平均一次
粒子径50Å)8質量%を混合してポニーミキサーにて
攬拌した後塗工機を用いてフィルム状に成形した。該フ
ィルムを円盤状に切断し、これを窒素雰囲気中の焼成炉
で500℃までを25℃/時の昇温速度で昇温し、その
後1400℃までを100℃/時で昇温し、1400℃
で3時間保持した後自然冷却して焼成を完了し、厚さ
1.0mmでクラスターダイヤモンド/アモルファス炭素
≒20/80の摺動特性試験片を得た。
(Example 2) Furan resin (Hitafuran VF-3 manufactured by Hitachi Chemical Co., Ltd.) as a hard amorphous carbon source
03) 8% by mass of cluster diamond (average primary particle size: 50 °) was mixed with 92% by mass of the mixture, and the mixture was stirred with a pony mixer, and then formed into a film using a coating machine. The film is cut into a disc shape, and the film is heated in a firing furnace in a nitrogen atmosphere up to 500 ° C. at a rate of 25 ° C./hour, and then up to 1400 ° C. at 100 ° C./hour. ° C
After holding for 3 hours, firing was completed by natural cooling to obtain a 1.0 mm thick cluster diamond / amorphous carbon / 20/80 sliding property test piece.

【0015】得られた試験片は、バウデン・レーベル型
ピン/ディスク摩擦試験機を用い、該試験片とR0.5
mmのアルミナピンとの組み合わせにり、すべり速度1.
7×10-3m/s、8.3×10-3m/s、荷重0.3
9N、1.5Nの低速度低荷重条件下での摩擦係数を測
定した。次にすべり速度100×10-3m/s、荷重
9.8Nで摩擦試験を行いディスク試料の比摩耗量を測
定した。
[0015] The obtained test piece was tested by using a Bowden-label type pin / disk friction tester.
Slip speed 1.
7 × 10 −3 m / s, 8.3 × 10 −3 m / s, load 0.3
The coefficient of friction under low speed and low load conditions of 9N and 1.5N was measured. Next, a friction test was performed at a sliding speed of 100 × 10 −3 m / s and a load of 9.8 N to measure the specific wear of the disk sample.

【0016】測定結果を表2に示す。本実施例による
と、以下に述べる比較例5、6に比べ優れた摺動特性を
有する摺動材を得られることがわかった。 (実施例3)硬質なアモルファス炭素源としてのフラン
樹脂(日立化成社製 ヒタフランVF−303)96質
量%にクラスターダイヤモンド(平均一次粒子径50
Å)4質量%を混合してポニーミキサーにて攬拌した後
塗工機を用いてフィルム状に成形した。該フィルムを円
盤状に切断し、これを窒素雰囲気中の焼成炉で500℃
までを25℃/時の昇温速度で昇温し、その後1400
℃までを100℃/時で昇温し、1400℃で3時間保
持した後自然冷却して焼成を完了し、厚さ1.0mmでク
ラスターダイヤモンド/アモルファス炭素≒10/90
の摺動特性試験片を得た。
Table 2 shows the measurement results. According to this example, it was found that a sliding material having better sliding characteristics than Comparative Examples 5 and 6 described below could be obtained. Example 3 A 96% by mass furan resin (Hitafuran VF-303 manufactured by Hitachi Chemical Co., Ltd.) as a hard amorphous carbon source was added to cluster diamond (average primary particle diameter 50).
Ii) 4% by mass was mixed and the mixture was stirred with a pony mixer, and then formed into a film using a coating machine. The film was cut into a disk shape, and this was fired at 500 ° C. in a firing furnace in a nitrogen atmosphere.
Up to 25 ° C./hour at a heating rate of
The temperature was raised to 100 ° C./hour, maintained at 1400 ° C. for 3 hours, and then naturally cooled to complete the calcination, and the cluster diamond / amorphous carbon having a thickness of 1.0 mm was obtained.
Specimens of the sliding characteristics were obtained.

【0017】得られた試験片は実施例2と同様に摺動試
験を実施した。その結果、表2に示すように本実施例に
よると、以下に述べる比較例5、6に比べ優れた摺動特
性を有する摺動材を得られることがわかった。 (比較例5)硬質なアモルファス炭素源としてのフラン
樹脂(日立化成社製 ヒタフランVF−303)98質
量%にクラスターダイヤモンド(平均一次粒子径50
Å)2質量%を混合してポニーミキサーにて攬拌した後
塗工機を用いてフィルム状に成形した。該フィルムを円
盤状に切断し、これを窒素雰囲気中の焼成炉で500℃
までを25℃/時の昇温速度で昇温し、その後1400
℃までを100℃/時で昇温し、1400℃で3時間保
持した後自然冷却して焼成を完了し、厚さ1.0mmでク
ラスターダイヤモンド/アモルファス炭素≒4/96の
摺動特性試験片を得た。
A sliding test was performed on the obtained test piece in the same manner as in Example 2. As a result, as shown in Table 2, according to this example, it was found that a sliding material having better sliding characteristics than Comparative Examples 5 and 6 described below could be obtained. Comparative Example 5 98% by mass of a furan resin (Hitafuran VF-303 manufactured by Hitachi Chemical Co., Ltd.) as a hard amorphous carbon source was added to cluster diamond (average primary particle size: 50).
Ii) 2% by mass was mixed and the mixture was stirred with a pony mixer, and then formed into a film using a coating machine. The film was cut into a disk shape, and this was fired at 500 ° C. in a firing furnace in a nitrogen atmosphere.
Up to 25 ° C./hour at a heating rate of
The temperature was raised to 100 ° C / hour at 100 ° C, held at 1400 ° C for 3 hours, and then cooled naturally to complete firing, and a 1.0 mm thick cluster diamond / amorphous carbon # 4/96 sliding property test piece I got

【0018】得られた試験片は実施例2と同様に摺動試
験を実施したが、表2に示すように実施例2、3に比べ
て摺動特性が劣っていた。 (比較例6)フラン樹脂(日立化成社製 ヒタフランV
F−303)を後塗工機を用いてフィルム状に成形し
た。該フィルムを円盤状に切断し、これを窒素雰囲気中
の焼成炉で500℃までを25℃/時の昇温速度で昇温
し、その後1400℃までを100℃/時で昇温し、1
400℃で3時間保持した後自然冷却して焼成を完了
し、厚さ1.0mmのアモルファス炭素のみからなる摺動
特性試験片を得た。
The obtained test piece was subjected to a sliding test in the same manner as in Example 2. As shown in Table 2, the sliding properties were inferior to those of Examples 2 and 3. (Comparative Example 6) Furan resin (Hitafuran V manufactured by Hitachi Chemical Co., Ltd.)
F-303) was formed into a film using a post-coating machine. The film is cut into a disc shape, and the film is heated in a firing furnace in a nitrogen atmosphere up to 500 ° C. at a rate of 25 ° C./hour, and then up to 1400 ° C. at 100 ° C./hour.
After holding at 400 ° C. for 3 hours, the mixture was naturally cooled to complete the firing, and a sliding property test piece having a thickness of 1.0 mm and comprising only amorphous carbon was obtained.

【0019】得られた試験片は実施例2と同様に摺動試
験を実施したが表2に示すように実施例2、3に比べて
摺動特性が劣っていた。
The test piece thus obtained was subjected to a sliding test in the same manner as in Example 2. However, as shown in Table 2, the sliding properties were inferior to those of Examples 2 and 3.

【0020】[0020]

【表2】 [Table 2]

【0021】[0021]

【発明の効果】本発明の炭素系摺動材料は、従来の炭素
材料に比べ低速度低荷重条件における平均摩擦係数、比
摩耗量が小さいなどの優れた摺動特性を有している。ま
た既存のプラスチックの成形方法を用いた本願発明では
焼成後に加工することなく任意の形状体を得ることが出
来るようになったため、従来の炭素系摺動材料とは異な
り、簡便な工程で、安価に製品を提供することが可能で
ある。
The carbon-based sliding material of the present invention has excellent sliding characteristics such as a small average friction coefficient and a small specific wear under low-speed and low-load conditions compared to conventional carbon materials. In addition, in the present invention using the existing plastic molding method, an arbitrary shaped body can be obtained without processing after firing, so unlike a conventional carbon-based sliding material, it is a simple process and is inexpensive. Products.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 3J011 DA01 DA02 SC01 SC02 SC14 SC16 SC20 SE02 4G032 AA01 AA04 AA06 AA07 AA13 AA14 BA03  ────────────────────────────────────────────────── ─── Continued on the front page F-term (reference) 3J011 DA01 DA02 SC01 SC02 SC14 SC16 SC20 SE02 4G032 AA01 AA04 AA06 AA07 AA13 AA14 BA03

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 クラスターダイヤモンドを含む炭素粉末
とアモルファス炭素とから実質的に成る炭素系摺動材
料。
1. A carbon-based sliding material consisting essentially of carbon powder containing cluster diamond and amorphous carbon.
【請求項2】 前記クラスターダイヤモンドが5質量%
以上含まれる請求項1記載の炭素系摺動材料。
2. The method according to claim 1, wherein the cluster diamond is 5% by mass.
The carbon-based sliding material according to claim 1, which is included.
【請求項3】 前記アモルファス炭素は、焼成後実質的
に零でない炭素残査収率を示す熱可塑性樹脂、熱硬化性
樹脂、天然高分子および合成高分子からなる群から選ば
れた高分子物質の1種または2種以上の混合物を出発原
料とする請求項1または2に記載の炭素系摺動材料。
3. The amorphous carbon is a polymer material selected from the group consisting of a thermoplastic resin, a thermosetting resin, a natural polymer and a synthetic polymer exhibiting a carbon residue yield that is not substantially zero after firing. The carbon-based sliding material according to claim 1 or 2, wherein one or a mixture of two or more thereof is used as a starting material.
【請求項4】 無潤滑剤下で滑り速度500×10-3
/s以下および荷重50N以下の低速度低荷重条件にお
ける平均摩擦係数が0.1以下である請求項1記載の炭
素系摺動材料。
4. A sliding speed of 500 × 10 −3 m without lubricant.
2. The carbon-based sliding material according to claim 1, wherein the average friction coefficient is 0.1 or less under low-speed and low-load conditions of 50 / s or less and a load of 50 N or less.
【請求項5】 アモルファス炭素の出発原料にクラスタ
ーダイヤモンドを含む炭素粉末を混合し、任意の形状に
賦形後、焼成することを特徴とする炭素系摺動材料の製
造方法。
5. A method for producing a carbon-based sliding material, comprising mixing a carbon powder containing cluster diamond with a starting material of amorphous carbon, shaping the mixture into an arbitrary shape, and firing.
【請求項6】 前記出発原料は、熱可塑性樹脂、熱硬化
性樹脂、天然高分子および合成高分子からなる群から選
ばれた高分子物質の1種または2種以上の混合物である
請求項5記載の炭素系摺動材料の製造方法。
6. The starting material is one or a mixture of two or more polymer substances selected from the group consisting of a thermoplastic resin, a thermosetting resin, a natural polymer and a synthetic polymer. A method for producing the carbon-based sliding material according to the above.
JP2000147490A 1999-10-13 2000-05-15 Carbon-based sliding material and manufacturing method thereof Expired - Fee Related JP4753455B2 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116143518A (en) * 2021-11-23 2023-05-23 燕山大学 Conductive high-strength diamond/amorphous carbon composite material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116143518A (en) * 2021-11-23 2023-05-23 燕山大学 Conductive high-strength diamond/amorphous carbon composite material and preparation method thereof
EP4183760A1 (en) * 2021-11-23 2023-05-24 Yanshan University Conductive diamond/amorphous carbon composite material having high strength and process for preparing the same

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