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JPH0343229B2 - - Google Patents
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JPH0343229B2 - - Google Patents

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Publication number
JPH0343229B2
JPH0343229B2 JP60036491A JP3649185A JPH0343229B2 JP H0343229 B2 JPH0343229 B2 JP H0343229B2 JP 60036491 A JP60036491 A JP 60036491A JP 3649185 A JP3649185 A JP 3649185A JP H0343229 B2 JPH0343229 B2 JP H0343229B2
Authority
JP
Japan
Prior art keywords
sintered sic
unreacted
ceramics
solid lubricant
sic
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 - Lifetime
Application number
JP60036491A
Other languages
Japanese (ja)
Other versions
JPS61197483A (en
Inventor
Yasushi Hoshi
Hideyuki Kurosawa
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.)
Riken Corp
Original Assignee
Riken Corp
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 Riken Corp filed Critical Riken Corp
Priority to JP3649185A priority Critical patent/JPS61197483A/en
Publication of JPS61197483A publication Critical patent/JPS61197483A/en
Publication of JPH0343229B2 publication Critical patent/JPH0343229B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Sliding-Contact Bearings (AREA)
  • Lubricants (AREA)
  • Ceramic Products (AREA)
  • Braking Arrangements (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はセラミツクスの摺動特性を改良したセ
ラミツクス摺動部材の製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method of manufacturing a ceramic sliding member in which the sliding characteristics of ceramics are improved.

(従来の技術と問題点) 近年セラミツクス材料に関する関心が高まり、
セラミツクスのもつ優れた耐摩耗、耐蝕性、耐熱
性、断熱性等に着目して各種摺動部材での応用が
なされている。しかしながらその多くは油潤滑が
豊富な状態での使用であり、潤滑油を供給できな
い部分や潤滑油を保持させることができない部分
での使用はほとんどなされていない。又高温にさ
らされる部分では潤滑しようとしても潤滑油の粘
度が著じるしく低下し潤滑目的を果すことができ
ない。
(Conventional technology and problems) In recent years, interest in ceramic materials has increased,
Ceramics are being applied to various sliding parts by focusing on their excellent wear resistance, corrosion resistance, heat resistance, heat insulation properties, etc. However, most of them are used in conditions where oil lubrication is abundant, and they are rarely used in areas where lubricating oil cannot be supplied or where lubricating oil cannot be retained. Furthermore, even if an attempt is made to lubricate parts exposed to high temperatures, the viscosity of the lubricating oil will drop significantly and the lubricating purpose cannot be achieved.

このように油潤滑ができないため固体潤滑に頼
るほかないが二硫化モリブデンやテフロン等の固
体潤滑剤の単体では耐熱性、強度の面から多くの
問題がある。油潤滑ができず又は高温にさらされ
る構造部材の需要が増加しており耐摩性、耐熱性
の高いセラミツクスを母材としその摺動性をたか
める方法の開発が期待されている。
Since oil lubrication is not possible, solid lubricants have no choice but to rely on solid lubricants, but solid lubricants such as molybdenum disulfide and Teflon have many problems in terms of heat resistance and strength. Demand for structural members that cannot be lubricated with oil or that are exposed to high temperatures is increasing, and there are expectations for the development of a method to increase the sliding properties of ceramics, which have high wear resistance and heat resistance, as a base material.

(問題点を解決するための手段) 第1図、第2図に示すように反応焼結SiCの表
層部の未反応部Si2を化学的或いは電気的に溶出
させた微細な空洞部3を形成し散在させたセラミ
ツクスを母材とし、該空洞部3に摺動特性の優れ
た固体潤滑剤を含浸し固着させて固体潤滑層4を
形成して固体潤滑性を保有させて耐熱性、耐摩性
等に優れたセラミツクスと油潤滑が不可能なきび
しい条件下でも潤滑性を維持できる固体潤滑剤と
を組合わせた新しいセラミツクス摺動部材の製造
方法を提供するものである。
(Means for solving the problem) As shown in Figs. 1 and 2, fine cavities 3 are formed by chemically or electrically eluting unreacted Si2 in the surface layer of reactive sintered SiC. A solid lubricant with excellent sliding properties is impregnated into the cavity 3 and fixed thereon to form a solid lubricant layer 4, which retains solid lubricity and has heat resistance and wear resistance. The present invention provides a new method for manufacturing a ceramic sliding member that combines ceramics with excellent properties such as ceramics and a solid lubricant that can maintain lubricity even under severe conditions where oil lubrication is impossible.

母材となる本発明の反応焼結SiCセラミツクス
は通常の反応焼結によるもので未反応のSi部分を
有するもので良い。
The reactively sintered SiC ceramic of the present invention, which serves as the base material, may be one that is produced by ordinary reactive sintering and has an unreacted Si portion.

反応焼結SiCの表層部の空洞部3のSiと反応す
る酸、フツ酸もしくはその混酸により化学的に溶
出させるか或いは反応焼結SiCを陽極とした電気
分解によるSi部分の溶出によつて得られる。電気
分解に用いられる電解質溶液はフツ酸を含む混酸
もしくはそれに類似した酸であればよい。
It can be obtained by chemically eluting the Si portion with an acid, hydrofluoric acid, or a mixed acid thereof that reacts with Si in the cavity 3 of the surface layer of the reactive sintered SiC, or by eluting the Si portion by electrolysis using the reactive sintered SiC as an anode. It will be done. The electrolyte solution used for electrolysis may be a mixed acid containing hydrofluoric acid or an acid similar thereto.

この空洞部3の固体潤滑剤としてステアリン酸
亜鉛、二硫化モリブデン、グラフアイト等を圧入
などの機械的方法又はグラフアイト等のコロイド
溶液中で電気泳動による化学的方法又は蒸着、ス
パツタリングなどの物理的方法を用いて該空洞部
に固体潤滑剤を含浸し固着させて固体潤滑層4を
形成させる。固体潤滑層の厚さtは空洞部3を形
成する未反応Si2の溶出の条件、固体潤滑剤の含
浸条件を適宜設定することにより、夫々の用途に
適した厚みが得られる。
As a solid lubricant for this cavity 3, zinc stearate, molybdenum disulfide, graphite, etc. are added mechanically by press-fitting, chemically by electrophoresis in a colloidal solution such as graphite, or physically by vapor deposition, sputtering, etc. A solid lubricant layer 4 is formed by impregnating and fixing a solid lubricant into the cavity using a method. The thickness t of the solid lubricant layer can be determined to be suitable for each application by appropriately setting the conditions for elution of unreacted Si2 forming the cavity 3 and the conditions for impregnating the solid lubricant.

(実施例) 本発明の実施例を本発明の構成によるセラミツ
クス摺動材料の特性を第3図ないし第5図の実験
データに基き説明する。
(Example) In an example of the present invention, the characteristics of a ceramic sliding material according to the structure of the present invention will be explained based on the experimental data shown in FIGS. 3 to 5.

実施例 1 反応焼結SiCの未反応Si部分をフツ化水素酸と
硝酸との混酸による化学的方法にて溶出を行なつ
た。
Example 1 The unreacted Si portion of reactive sintered SiC was eluted by a chemical method using a mixed acid of hydrofluoric acid and nitric acid.

フツ化水素酸(47%):硝酸:水=1:1:1
の割合の混酸中で反応焼結SiCの未反応Siを溶出
させた。
Hydrofluoric acid (47%): Nitric acid: Water = 1:1:1
The unreacted Si of the reacted sintered SiC was eluted in a mixed acid with a ratio of .

反応時間と溶出深さとの関係を第3図に示す。
反応時間1時間及び2時間における溶出深さは
0.3mm、0.6mmと反応時間と溶出深さとはほぼ比例
している。
The relationship between reaction time and elution depth is shown in Figure 3.
The elution depth at reaction times of 1 hour and 2 hours is
At 0.3 mm and 0.6 mm, the reaction time and elution depth are almost proportional.

実施例 2 実施例1において空洞深さ0.3mmの試料にステ
アリン酸亜鉛の含浸を圧入方法により行なつた。
Example 2 In Example 1, a sample having a cavity depth of 0.3 mm was impregnated with zinc stearate by the press injection method.

含浸方法は含浸槽のステアリン酸溶液の液温
230℃、試料を雰囲気温度230℃に30分間保持して
230℃に保温した後−700mmHg以下に減圧した含
浸槽の液中に漬けて5分間保持後含浸槽を0.9
Kg/cm2に加圧し3分間保持後含浸液を抜き回転遠
心力により液切りし取り出した。
The impregnation method is based on the temperature of the stearic acid solution in the impregnation tank.
230℃, keeping the sample at the ambient temperature of 230℃ for 30 minutes.
After keeping the temperature at 230℃, immerse it in the liquid of the impregnation tank that has been reduced to -700mmHg or less, hold it for 5 minutes, and then reduce the pressure to 0.9
After pressurizing to Kg/cm 2 and holding for 3 minutes, the impregnating liquid was drained and the liquid was drained by rotating centrifugal force and taken out.

本方法による含浸率は90%であつた。 The impregnation rate by this method was 90%.

実施例 3 反応焼結SiCの未反応Si部分を電気分解による
電気的方法にて溶出を行なつた。
Example 3 The unreacted Si portion of reactive sintered SiC was eluted by an electrical method using electrolysis.

フツ化水素酸(47%)5容量%、硝酸、5容量
%水溶液中で陽極を反応焼結SiC、陰極をCu板と
して定電圧電解を行なつた。
Constant voltage electrolysis was carried out in an aqueous solution of 5% by volume of hydrofluoric acid (47%) and 5% by volume of nitric acid, with reaction sintered SiC as the anode and a Cu plate as the cathode.

電流密度と単位面積当りの溶出量との関係は第
4図に示す通りであり、電流密度3及び5×
10-2A/cm2のときの溶出量は7と12×10-3gと電
流密度と溶出量はほぼ比例している。
The relationship between current density and elution amount per unit area is as shown in Figure 4.
The elution amount at 10 -2 A/cm 2 is 7 and 12×10 -3 g, and the current density and elution amount are almost proportional.

実施例 4 実施例3の未反応Siの溶出深さ0.3mmの試料に
グラフアイトの含浸を電気泳動による化学的方法
により行なつた。
Example 4 The sample of Example 3 with an elution depth of 0.3 mm was impregnated with graphite by a chemical method using electrophoresis.

0.5容量%のグラフアイト溶液中で反応焼結SiC
を陽極、Cu板を陰極として電圧を加えて電気泳
動させた。
Reactive sintered SiC in 0.5% by volume graphite solution
Electrophoresis was performed by applying a voltage using the Cu plate as an anode and the Cu plate as a cathode.

含浸率は85%であつた。 The impregnation rate was 85%.

実施例 5 上記実施例2、4の試料について潤滑特性の試
験を行なつた。
Example 5 The samples of Examples 2 and 4 above were tested for lubricating properties.

ピンホンデイスク摩擦試験機で摩擦速度0.23
m/s、荷重20Kg/cm2無潤滑の条件にて試験を
行なつた。試験結果の摩擦係数は第5図に示す通
りである。
Friction speed 0.23 with Pinghon disk friction tester
The test was conducted under the following conditions: m/s, load 20 kg/cm 2 and no lubrication. The friction coefficient of the test results is as shown in FIG.

比較例として試験を行なつた反応焼結SiCの摩
擦係数値0.2に対しステアリン酸亜鉛含浸SiC0.1、
グラフアイト含浸SiC0.09と摩擦係数は半減し潤
滑性は大巾に向上した。
The friction coefficient value of reactive sintered SiC tested as a comparative example was 0.2, whereas the friction coefficient of zinc stearate-impregnated SiC was 0.1;
With graphite-impregnated SiC0.09, the friction coefficient was halved and the lubricity was greatly improved.

効 果 本発明によればセラミツクスの優れた耐熱性、
耐摩性と固体潤滑剤の低摩擦特性との相乗効果に
より油潤滑の不可能なきびしい条件下で或いは使
用が好ましくない環境下で使用される摺動部材と
して、潤滑油を供給することなく自己潤滑性をも
つた耐摩性、耐蝕性、耐熱性等の諸特性の優れた
摺動部材を得ることができるという顕著な効果が
ある。
Effects According to the present invention, ceramics have excellent heat resistance,
Due to the synergistic effect of wear resistance and the low friction properties of solid lubricants, it can self-lubricate without supplying lubricating oil as a sliding member used under severe conditions where oil lubrication is impossible or in environments where use is undesirable. This has the remarkable effect that it is possible to obtain a sliding member with excellent properties such as wear resistance, corrosion resistance, and heat resistance.

【図面の簡単な説明】[Brief explanation of drawings]

第1図 本発明の実施例を示す断面模式図。第
2図 セラミツクスの一般的な断面模式図。第3
図 未反応Siを化学的方法で溶出した反応時間と
溶出深さとの関係線図。第4図 未反応Siを電気
的方法で溶出した電流密度と溶出量との関係線
図。第5図 反応焼結SiCと本発明のSi−Zn含浸
SiC、グラフアイト含浸SiCの摩擦係数を示す。 1:SiC粒子、2:未反応Si、3:空洞部、
4:固体潤滑層。
FIG. 1 is a schematic cross-sectional view showing an embodiment of the present invention. Figure 2: General cross-sectional diagram of ceramics. Third
Figure: Relationship diagram between reaction time and elution depth when unreacted Si is eluted using a chemical method. Figure 4: Relationship diagram between current density and elution amount when unreacted Si is eluted by an electrical method. Figure 5 Reactive sintered SiC and Si-Zn impregnation of the present invention
The friction coefficient of SiC and graphite-impregnated SiC is shown. 1: SiC particles, 2: unreacted Si, 3: cavity,
4: Solid lubricant layer.

Claims (1)

【特許請求の範囲】[Claims] 1 反応焼結SiCの表層部の未反応部Siを化学的
或いは電気的に溶出させて微細な空洞部を形成し
散在させたセラミツクスを母材とし、該空洞部に
摺動特性の優れた固体潤滑剤を含浸し固着させて
固体潤滑層を形成させたことを特徴とする反応焼
結SiCセラミツクス摺動部材の製造方法。
1 The base material is ceramics in which the unreacted Si in the surface layer of reactive sintered SiC is chemically or electrically eluted to form fine cavities and dispersed therein, and the cavities are filled with a solid material with excellent sliding properties. A method for manufacturing a reaction sintered SiC ceramic sliding member, characterized in that a solid lubricant layer is formed by impregnating and fixing a lubricant.
JP3649185A 1985-02-27 1985-02-27 Ceramic sliding member Granted JPS61197483A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3649185A JPS61197483A (en) 1985-02-27 1985-02-27 Ceramic sliding member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3649185A JPS61197483A (en) 1985-02-27 1985-02-27 Ceramic sliding member

Publications (2)

Publication Number Publication Date
JPS61197483A JPS61197483A (en) 1986-09-01
JPH0343229B2 true JPH0343229B2 (en) 1991-07-01

Family

ID=12471291

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3649185A Granted JPS61197483A (en) 1985-02-27 1985-02-27 Ceramic sliding member

Country Status (1)

Country Link
JP (1) JPS61197483A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62270481A (en) * 1986-05-15 1987-11-24 株式会社日立製作所 Ceramics for sliding materials
US20080248318A1 (en) * 2005-08-25 2008-10-09 Boise White Paper, L.L.C. Low-Opacity Release Paper, Release-Paper Backing and Methods

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5864284A (en) * 1981-10-09 1983-04-16 信越化学工業株式会社 Manufacture of silicon carbide sintered body
JPS59232981A (en) * 1983-06-15 1984-12-27 株式会社日立製作所 Ceramic sliding material

Also Published As

Publication number Publication date
JPS61197483A (en) 1986-09-01

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