JPH0288744A - Cr2o3-mo sintered body - Google Patents

Cr2o3-mo sintered body

Info

Publication number
JPH0288744A
JPH0288744A JP23820088A JP23820088A JPH0288744A JP H0288744 A JPH0288744 A JP H0288744A JP 23820088 A JP23820088 A JP 23820088A JP 23820088 A JP23820088 A JP 23820088A JP H0288744 A JPH0288744 A JP H0288744A
Authority
JP
Japan
Prior art keywords
sintered body
cr2o3
resistance
present
wear
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
JP23820088A
Other languages
Japanese (ja)
Inventor
Yoshihisa Kitajima
北嶋 義久
Masanori Tanaka
正紀 田中
Shuzo Hirata
修三 平田
Takashi Nakamura
中村 高司
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.)
Mitsui Engineering and Shipbuilding Co Ltd
Original Assignee
Mitsui Engineering and Shipbuilding 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 Mitsui Engineering and Shipbuilding Co Ltd filed Critical Mitsui Engineering and Shipbuilding Co Ltd
Priority to JP23820088A priority Critical patent/JPH0288744A/en
Publication of JPH0288744A publication Critical patent/JPH0288744A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To permit the thickening of the title sintered body as a wear-resistant material and to improve its seizure resistance by specifying the content of Cr2O3 and Mo in a sintered body. CONSTITUTION:In a composite material sintered body, as the compsn., by weight, 30 to 90% Cr2O3) and 10 to 70% Mo are regulated and the total of Cr2O3 and Mo is regulated to 70 to 100%. In addition to trace amounts of impurities included in the material, a sintering auxiliary and the elements to improve corrosion resistance, strength, etc., can be incorporated into the sintered body. The Cr2O3-Mo sintered body is a composite material contg. Mo of high m.p. metal and Cr2O3 of ceramics having high hardness. Thus, the material combines high toughness of Mo and heat resistance, high hardness and chemical stability of Cr2O3 to improve the wear resistance of the sintered body. The sintered body is furthermore applicable to a member having complicated shape.

Description

【発明の詳細な説明】 [産業上の利用分野コ 本発明はCr2O3−Mo系焼結体に係り、特にCr、
、03とMOとを複合化することにより、Cr2O2の
極めて優れた耐摩耗性を維持しつつ、Moによる高靭性
化を図り、潤滑剤の保持特性が高く耐摩耗性に著しく優
れた部材を提供するCr2O3Mo系焼結体に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a Cr2O3-Mo based sintered body, in particular Cr,
By combining , 03 and MO, we can maintain the extremely excellent wear resistance of Cr2O2 while increasing the toughness of Mo, providing a member with high lubricant retention properties and extremely excellent wear resistance. The present invention relates to a Cr2O3Mo-based sintered body.

[従来の技術] 機械部品や各種装置の構成材料は、十分な機械的強度以
外に、使用目的に応じた耐摩耗性、耐食性等の特性を備
えていることが必要となるが、耐摩耗性の高い材料は、
多くの場合靭性が低いなど、1種類の材料では2以上の
特性を同時に具備せしめることは容易ではない。
[Prior Art] In addition to sufficient mechanical strength, the constituent materials of mechanical parts and various devices must have properties such as wear resistance and corrosion resistance depending on the purpose of use. Materials with high
It is not easy for one type of material to have two or more properties at the same time, such as low toughness in many cases.

そこで、部材表面に耐摩耗性の高い材料を被覆する表面
処理法が種々開発されており、例えば、モリブデン(M
O)又はMo合金とCr2Ozを原料として、部材表面
に溶射して特定配合のM。
Therefore, various surface treatment methods have been developed to coat the surface of parts with highly wear-resistant materials. For example, molybdenum (M
O) or Mo alloy and Cr2Oz are used as raw materials, and M is sprayed onto the surface of the member to form a specific blend.

又はMo合金とCr2O3とから構成される耐摩耗性被
膜を形成する方法が特許出願されている(特願昭61−
157111号。以下「先願」という。)。
Alternatively, a patent application has been filed for a method of forming a wear-resistant coating composed of Mo alloy and Cr2O3 (Japanese Patent Application No. 1986-
No. 157111. Hereinafter referred to as "prior application". ).

[発明が解決しようとする課題] 先願に係る耐摩耗性被膜は、溶射被膜であることから、
次のような不具合があった。
[Problem to be solved by the invention] Since the wear-resistant coating according to the prior application is a thermally sprayed coating,
There were the following problems.

■ 厚肉化ができない。最大厚さは0.5mm程度で、
それ以上の厚肉化は困難である。
■ Cannot be made thicker. The maximum thickness is about 0.5mm,
It is difficult to increase the thickness further.

■ 溶射法は適用できる部材形状に制限があり、部材の
形状によっては溶射被膜を形成できない場合がある。例
えば、内径10mmX長さ50mmといった小径シリン
ダーの内面に溶射被膜を形成することは非常に困難であ
る。
■ Thermal spraying method has limitations on the shape of parts to which it can be applied, and depending on the shape of the part, it may not be possible to form a sprayed coating. For example, it is extremely difficult to form a thermal spray coating on the inner surface of a cylinder with a small diameter of 10 mm in inner diameter and 50 mm in length.

本発明は、このような問題点を解決し、耐摩耗性材料と
して、厚肉化が可能で複雑形状部材にも十分適用するこ
とができるCr2O2Mo系焼結体を提供することを目
的とする。
An object of the present invention is to solve these problems and provide a Cr2O2Mo-based sintered body as a wear-resistant material that can be made thick and can be sufficiently applied to members with complex shapes.

[課題を解決するための手段] 本発明のCr2o、、−Mo系焼結体は、30〜90重
量%のCr2O3と10〜70重量%のMoを含み、か
つCr2O3とMoとの合計が70〜100重量%であ
ることを特徴とする。
[Means for Solving the Problems] The Cr2o, -Mo-based sintered body of the present invention contains 30 to 90% by weight of Cr2O3 and 10 to 70% by weight of Mo, and the total of Cr2O3 and Mo is 70% by weight. ~100% by weight.

以下に本発明の詳細な説明する。The present invention will be explained in detail below.

まず、本発明のCr2 o2−Mo系焼結体の製造方法
について、その具体的方法を示す系統図である第1図を
参照して説明する。
First, the method for producing a Cr2o2-Mo based sintered body of the present invention will be described with reference to FIG. 1, which is a system diagram showing a specific method.

本発明のCr2Oz  Mo系焼結体の製造にあたって
は、まず、焼結用原料粉末を製造する。
In producing the Cr2Oz Mo-based sintered body of the present invention, first, raw material powder for sintering is produced.

焼結用原料粉末の製造方法としては、例えば次の方法が
挙げられる。
Examples of the method for producing the raw material powder for sintering include the following method.

■ Cr2O5、Mo (又はMo合金)及び焼結助剤
、その他の添加物を機械的に混合する(第1図のAルー
ト)。この方法は操作が簡単で処理コストが安価である
という利点がある。
■ Mechanically mix Cr2O5, Mo (or Mo alloy), sintering aid, and other additives (Route A in Figure 1). This method has the advantage of being easy to operate and having low processing costs.

■ Cr2O3とMo(又はMo合金)を混合、溶融、
粉砕、分級し複合粉末を製造した後、これに焼結助剤、
その他の添加物を加えて機械的に混合する(第1図のB
ルート)。この方法は、Cr2O3とMOとを微細に分
散させることができ、得られる焼結体が強靭化するとい
う利点がある。
■ Mixing and melting Cr2O3 and Mo (or Mo alloy),
After pulverizing and classifying to produce composite powder, sintering aids,
Add other additives and mix mechanically (B in Figure 1).
root). This method has the advantage that Cr2O3 and MO can be finely dispersed, and the resulting sintered body is toughened.

なお、この方法において、溶融方法としては特に制限は
ないが、アーク溶解法が好適である。溶融に際しては、
加熱溶解時にMOが酸化されるなどして原料が変質する
のを防止するために、Arガス等の不活性ガス雰囲気下
で加熱溶解するのが好ましい。その他、10””Tor
r以下の真空下での電子ビームによる加熱溶解法も採用
可能である。溶融は、混合粉末が溶融する温度であれば
良く、通常はMo又はMo合金の溶融温度以上で行なわ
れる。
In this method, the melting method is not particularly limited, but arc melting is preferred. When melting,
In order to prevent the raw material from changing in quality due to oxidation of MO during heating and melting, it is preferable to heat and melt in an inert gas atmosphere such as Ar gas. Others, 10””Tor
It is also possible to employ a heating melting method using an electron beam under a vacuum of r or less. Melting may be carried out at a temperature at which the mixed powder melts, and is usually carried out at a temperature equal to or higher than the melting temperature of Mo or Mo alloy.

本発明において、このようにして得られる焼結用原料粉
末は、その粒径が1〜5μm程度であることが好ましい
。粒径が5μmを超えると高密度焼結体を得るのが困難
であり、1μm未満ではCr2O3とMoの複合材料が
過度に粉砕された結果、Cr2O3とMoに再び分離さ
れた粒子が多く、高靭性の焼結体を得ることが困難であ
る。
In the present invention, the raw material powder for sintering obtained in this manner preferably has a particle size of about 1 to 5 μm. If the particle size exceeds 5 μm, it is difficult to obtain a high-density sintered body, and if the particle size is less than 1 μm, the composite material of Cr2O3 and Mo will be crushed excessively, and many particles will be separated into Cr2O3 and Mo again, resulting in a high-density sintered body. It is difficult to obtain a tough sintered body.

次に、得られた焼結用原料粉末を焼結する。Next, the obtained raw material powder for sintering is sintered.

焼結方法としては、例えば次の方法が挙げられる。Examples of the sintering method include the following method.

■ ホットプレス又はHIP法により加圧焼結する(第
1図のCルート)。具体的には、Mo製容器等に原料粉
末を充填し、容器内を真空引きした後密封し、熱間静水
圧プレス等で加圧焼結する。この方法は、緻密度が高く
、高強度の焼結体が得られるという利点がある。
■ Pressure sintering by hot press or HIP method (Route C in Figure 1). Specifically, a Mo container or the like is filled with raw material powder, the inside of the container is evacuated, the container is sealed, and the container is sintered under pressure using a hot isostatic press or the like. This method has the advantage that a sintered body with high density and high strength can be obtained.

■ 焼結用原料粉末を造粒、圧粉後、不活性ガス中で常
圧焼結する(第1図のDルート)、、この方法は、特殊
かつ高価な焼結装置が不要であるという利点がある。
■ The raw material powder for sintering is granulated, compacted, and then sintered under normal pressure in an inert gas (route D in Figure 1).This method does not require special and expensive sintering equipment. There are advantages.

本発明のCrCr2Os−系焼結体は、このような焼結
により所望形状の部材を製造することもでき、また、こ
れを更に切削加工するなどにより所望形状の部材とする
こともできる。
The CrCr2Os-based sintered body of the present invention can be manufactured into a member having a desired shape by such sintering, or can be further cut into a member having a desired shape.

本発明のCr 2O s  M o系焼結体は、部材の
形状、大きさを問わず、殆ど全ての部材に適用すること
ができる。例えば、前述の溶射を適用することが困難で
ある内径10 m m s長さ50mmといったシリン
ダーであれば、その全体を本発明のCr2O5−Mo系
焼結体とすることにより、あるいは適当な肉厚のスリー
ブを本発明のCrCr2Os−系焼結体で製作すること
により、容易に適用可能である。
The Cr2OsMo-based sintered body of the present invention can be applied to almost all members regardless of their shape and size. For example, if the cylinder has an inner diameter of 10 mm and a length of 50 mm, to which it is difficult to apply the thermal spraying described above, the entire cylinder may be made of the Cr2O5-Mo-based sintered body of the present invention, or the cylinder may be coated with an appropriate wall thickness. By making the sleeve of the CrCr2Os-based sintered body of the present invention, it can be easily applied.

次に、本発明のCr2O3−Mo系焼結体の成分組成に
ついて説明する。なお、以下において1%」は「重量%
」を示す。
Next, the composition of the Cr2O3-Mo based sintered body of the present invention will be explained. In addition, in the following, "1%" is "weight%"
” is shown.

本発明のCr 2 Os  M o系焼結体は、Cr2
o3の含有量をX%、MOの含有量をY%とじた場合、 X 千 30〜90 Y = 10〜70 70≦x +Y≦ 100 である。即ち、第2図に示すCr2O3とMOとの配合
割合の相関図において、 x=30 x;90 y=t。
The Cr2OsMo-based sintered body of the present invention has Cr2OsMo-based sintered body.
When the content of o3 is X% and the content of MO is Y%, X 1,000 30-90 Y = 10-70 70≦x +Y≦100. That is, in the correlation diagram of the mixing ratio of Cr2O3 and MO shown in FIG. 2, x=30 x; 90 y=t.

y=70 x+y=70 x+y=100 の線分で囲まれた領域、即ちa、b、c、d点で囲まれ
た領域である。
This is the area surrounded by the line segments y=70 x+y=70 x+y=100, that is, the area surrounded by points a, b, c, and d.

Cr2O3が30%未満であると、耐摩耗性に優れたC
r2O3の特性を充分発揮できず、焼結体の耐摩耗性等
が低下する。また、Cr2o3が90%を超えると、残
部が全てMoであっても、MOの量が相対的に少なくな
り、やはり複合化による十分な効果が得られず、焼結体
の靭性が低下するなどの不具合が生じる。
When Cr2O3 is less than 30%, C has excellent wear resistance.
The characteristics of r2O3 cannot be fully exhibited, and the wear resistance of the sintered body deteriorates. Furthermore, if Cr2o3 exceeds 90%, even if the remainder is entirely Mo, the amount of MO will be relatively small, and the sufficient effect of the composite will not be obtained, resulting in a decrease in the toughness of the sintered body, etc. This will cause problems.

MOが10%未満では、Moが少な過ぎるために複合化
による十分な効果が得られない。Moが70%を超える
と、残部が全てCr2O3の場合であっても、Cr2O
3は30%未満となり、Cr2O5の優れた耐摩耗性を
十分に生かすことができない。
If the MO content is less than 10%, the Mo content is too small and a sufficient effect cannot be obtained by compounding. When Mo exceeds 70%, even if the remainder is all Cr2O3, Cr2O
3 is less than 30%, and the excellent wear resistance of Cr2O5 cannot be fully utilized.

Cr2O3とMoとの比率は、焼結体の用途に応じて、
上記組成範囲内で適宜選択されるが、Cr2O3とMO
との合計量が70%未満では、Cr2O5とMoとの複
合化による耐摩耗性等の改善効果が十分に得られないの
で、両者の合計は70%以上とする。
The ratio of Cr2O3 and Mo depends on the use of the sintered body.
It is selected as appropriate within the above composition range, but Cr2O3 and MO
If the total amount of Cr2O5 and Mo is less than 70%, the effect of improving wear resistance etc. by combining Cr2O5 and Mo cannot be sufficiently obtained, so the total amount of both should be 70% or more.

本発明において% Cr2o3.Mo以外のその他の成
分含有量は、前記好適範囲の定義からは、30%未満と
される。Cr2O5、MO以外(Dその他の成分として
は、例えば、次の■〜■のようなものが挙げられる。
In the present invention, % Cr2o3. The content of other components other than Mo is less than 30% from the definition of the preferred range. Examples of components other than Cr2O5 and MO (D) include the following (1) to (2).

■ 原料のCr2O3に含まれる微量の不純物。■ Trace impurities contained in the raw material Cr2O3.

例えば、SiO2,TiO2,Fe2O3等。For example, SiO2, TiO2, Fe2O3, etc.

■ 原料のMoに含まれる微量の不純物。例えばFe、
Al1等。
■ Trace impurities contained in the raw material Mo. For example, Fe,
Al1 etc.

■ 原料としてMo合金を用いた場合の合金化元素及び
微量の不純物。例えば、Fe、All。
■ Alloying elements and trace impurities when Mo alloy is used as a raw material. For example, Fe, All.

Ni、Cr、Co、C等。Ni, Cr, Co, C, etc.

■ Mo又はMo合金あるいはCr2O2以外に、製造
工程において、焼結体の緻密化、結晶粒粗大化抑制等、
焼結助剤としての効果を得るために別途添加したもの。
■ In addition to Mo or Mo alloy or Cr2O2, in the manufacturing process, sintered bodies are densified, crystal grain coarsening is suppressed, etc.
Added separately to obtain the effect as a sintering aid.

例えば、TiO2,MgO,SiO2゜Y2 o、等。For example, TiO2, MgO, SiO2゜Y2 o, etc.

■ Mo又はMo合金あるいはCr2O3以外に、製造
工程において、焼結体の耐食性等の化学的性質の改善及
び/又は強度向上環の機械的性質の改善を図るために別
途添加したもの。
(2) In addition to Mo or Mo alloy or Cr2O3, something added separately in the manufacturing process to improve the chemical properties such as corrosion resistance of the sintered body and/or to improve the mechanical properties of the strength-enhancing ring.

例えば、Cr、Co、Ni、Ag、Ti。For example, Cr, Co, Ni, Ag, Ti.

Zr、Re、C等。Zr, Re, C, etc.

なお、本発明において、Mo合金を原料として用いる場
合、Mo合金としては、Fe50%以下、AiLIO%
以下、NilO%以下、Cr15%以下、Co10%以
下、03%以下含有するものが好ましい。
In addition, in the present invention, when using a Mo alloy as a raw material, the Mo alloy contains 50% or less Fe, AiLIO%
Hereinafter, it is preferable that the content is NilO% or less, Cr15% or less, Co10% or less, and Co3 or less.

Feは安価でありMo合金の価格を低下させることがで
きるが、過度に多いと耐摩耗性を損なうので、Feは3
0%以下とりわけ2O%以下とするのが好ましい。
Fe is cheap and can reduce the price of Mo alloy, but if it is present excessively, wear resistance will be impaired, so Fe is
It is preferably 0% or less, especially 20% or less.

AJZは金属組織の微細化を図り、その耐食性を高める
ことができるが、過度に多量であると耐摩耗性を損なう
ので、10%以下とりわけ7%以下とするのが好ましい
AJZ can refine the metal structure and improve its corrosion resistance, but if the amount is too large, it impairs wear resistance, so it is preferably 10% or less, especially 7% or less.

Niは基地の強化に有効であるが、過度に多くなると異
種組織を発生し易くなる。そのため、Niは10%以下
とりわけ7%以下とするのが好ましい。
Although Ni is effective in strengthening bases, excessive amounts of Ni tend to generate foreign tissue. Therefore, the Ni content is preferably 10% or less, especially 7% or less.

Crは基地の耐食性を高めるが、炭化物生成傾向が強く
、その含有量が過度に多くなると金属組織の靭性が低下
し易くなる。そこで、Crは15%以下とりわけ10%
以下とするのが好ましい。
Although Cr improves the corrosion resistance of the matrix, it has a strong tendency to form carbides, and if its content is excessively high, the toughness of the metal structure tends to decrease. Therefore, Cr is 15% or less, especially 10%
The following is preferable.

COは基地の強化に有効に作用するが、過度に多くなる
と基地の融点を低下させるので、10%以下とりわけ7
%以下とするのが好ましい。
CO has an effective effect on strengthening the base, but if it increases excessively, it lowers the melting point of the base, so it should not exceed 10%, especially 7%.
% or less.

Cは基地の耐焼付性、耐摩耗性を高める作用があるが、
過度に多くなると炭化物析出量が多くなったり、基地そ
れ自体の強度を低下させるので、3%以下とするのが好
ましい。
C has the effect of increasing the seizure resistance and wear resistance of the base,
If it increases too much, the amount of carbide precipitation increases and the strength of the base itself decreases, so it is preferably 3% or less.

[作用] 本発明のCr2O5−Mo系焼結体は、高融点金属であ
るMOと高硬度のセラミックスであるCr2O3とを含
む複合材料である。このため、Moの高靭性とCr 2
O2の耐熱性、高硬度、化学的安定性の両者を兼備する
極めて優れた焼結体である。この様に、高靭性と高硬度
を兼備することは、焼結体の耐摩耗性を著しく向上させ
ることになる。
[Function] The Cr2O5-Mo-based sintered body of the present invention is a composite material containing MO, which is a high melting point metal, and Cr2O3, which is a high hardness ceramic. For this reason, the high toughness of Mo and Cr2
It is an extremely excellent sintered body that has both O2 heat resistance, high hardness, and chemical stability. In this way, having both high toughness and high hardness significantly improves the wear resistance of the sintered body.

本発明の焼結体は、MO相がCr2O5母相に分散して
いる構造であるが、その表面が他の部材と摺動すると、
Cr2O3よりも硬度の低いM。
The sintered body of the present invention has a structure in which the MO phase is dispersed in the Cr2O5 matrix, but when its surface slides with other members,
M has lower hardness than Cr2O3.

相部が摩耗し、Cr2O3相部が被膜面から突出するよ
うにして露出し、表面に微小な多数の凹部が形成される
。この凹部は良好な潤滑剤の溜部として作用し、潤滑剤
の保持特性が著しく高くなり、耐摩耗性が著しく高いも
のとされる。
The phase portion is worn away, and the Cr2O3 phase portion is exposed to protrude from the coating surface, and many minute recesses are formed on the surface. This concave portion acts as a good lubricant reservoir, resulting in extremely high lubricant retention properties and extremely high wear resistance.

しかして、本発明のCr2Oa  Mo系焼結体は、こ
のような優れた特性を有するCr2O3−Mo系複合材
料の焼結晶であるため、様々な形状、大きさに対応する
ことができる。特に、溶射被膜に比し、厚肉化が可能で
あることから、前述の摺動による摩耗代を大きくとるこ
とができ、その結果、部材の長寿命化を図ることが可能
とされる。
Since the Cr2Oa Mo-based sintered body of the present invention is a sintered crystal of a Cr2O3-Mo-based composite material having such excellent properties, it can be made into various shapes and sizes. In particular, since the thickness can be increased compared to a thermally sprayed coating, the wear allowance due to the above-mentioned sliding can be increased, and as a result, it is possible to extend the life of the member.

[実施例] 以下、実施例及び比較例について説明する。[Example] Examples and comparative examples will be described below.

実施例1 粒径1〜5μmのer2O370%と、粒径1〜3μm
のMo29%と、焼結助材として粒径1〜5μmのTi
O21%を、機械的に混合した後、MO製容器内に充填
し、Mo容器内を真空引きした状態でMo容器を密封し
た。このMo容器ごと、熱間静水圧プレス機に入れ、t
soot。
Example 1 70% er2O3 with particle size 1-5 μm and particle size 1-3 μm
29% of Mo, and Ti with a particle size of 1 to 5 μm as a sintering aid.
After mechanically mixing O21%, it was filled into an MO container, and the Mo container was sealed while the inside of the Mo container was evacuated. Put this Mo container into a hot isostatic press machine, and
soot.

tookg/crrl’に加熱加圧し、1時間保持して
焼結を行なった。この様にして、直径60mm、厚さ1
5mmの円盤状の焼結体を作成した。
The material was heated and pressurized to tookg/crrl' and held for 1 hour to perform sintering. In this way, the diameter is 60 mm and the thickness is 1.
A 5 mm disk-shaped sintered body was created.

上記方法により同形状の焼結体を2個製造し、一方は表
面を研削加工して、第3図に示す厚さ13mm、直径5
8mmのディスク型試験片11とした。また、他方は、
切断及び切削加工により直径5mm、高さ6mmのビン
12aを形成し、円盤状のホルダ12bに固定してビン
型試験片12とした。
Two sintered bodies of the same shape were manufactured using the above method, and one was ground to a thickness of 13 mm and a diameter of 5 mm as shown in Figure 3.
A disk-shaped test piece 11 of 8 mm was prepared. Also, on the other hand,
A bottle 12a having a diameter of 5 mm and a height of 6 mm was formed by cutting and machining, and was fixed to a disk-shaped holder 12b to obtain a bottle-shaped test piece 12.

得られたビン型試験片(回転側)12及びディスク型試
験片(固定側)11を第4図に示す如く、回転力R及び
垂直荷重Wが加えられるようにセットして、第5図に示
す装置で、ビンオンディスク摩耗試験を行ない、摩耗量
を測定した。なお、第5図において、13はベルト、1
4はクラッチ、15はモーター 16は冷却油の流通管
、17は潤滑剤、18はエアシリンダである。
The obtained bottle-shaped test piece (rotating side) 12 and disc-shaped test piece (fixed side) 11 were set so that a rotational force R and a vertical load W were applied as shown in Fig. 5. A bottle-on-disc wear test was conducted using the equipment shown, and the amount of wear was measured. In addition, in FIG. 5, 13 is a belt, 1
4 is a clutch, 15 is a motor, 16 is a cooling oil flow pipe, 17 is a lubricant, and 18 is an air cylinder.

この時の実験条件は、第1表に示す通りである。The experimental conditions at this time are as shown in Table 1.

結果を第2表に示す。The results are shown in Table 2.

比較例1.2 比較のために、Cr2O3(加圧焼結体)製ディスク型
試験片及び同ビン型試験片(比較例1)、Mo(加圧焼
結体)製ディスク型試験片及び同ビン型試験片(比較例
2)についても、実施例1と同条件でピンオンディスク
摩耗試験を行なった。
Comparative Example 1.2 For comparison, a disk-shaped test piece made of Cr2O3 (pressure sintered body) and the same bottle-shaped test piece (Comparative Example 1), a disk-shaped test piece made of Mo (pressure sintered body) and the same bottle-type test piece were prepared. A pin-on-disc wear test was also conducted on the bottle-shaped test piece (Comparative Example 2) under the same conditions as in Example 1.

結果を第2表に示す。The results are shown in Table 2.

実施例2 84%Cr2O3+16%Moの組成の原料を、第6図
に示す溶解炉21にて溶融した。溶融にあたりては、ま
ず、バルブv1を開として真空ポンプ23により1xl
O−’Torrに真空引きした。次いでバルブV、を閉
、バルブ■2を開として純度99.99%のArガスを
導入し、溶解室22内の圧力を760Torrとした。
Example 2 A raw material having a composition of 84% Cr2O3 + 16% Mo was melted in a melting furnace 21 shown in FIG. For melting, first open the valve v1 and apply 1xl using the vacuum pump 23.
Vacuum was applied to O-' Torr. Next, valve V was closed and valve 2 was opened to introduce Ar gas with a purity of 99.99%, and the pressure in the melting chamber 22 was set to 760 Torr.

この状態で、溶解室22内のタングステン電極(−極)
24と水冷した銅坩堝(子種)25(図中、26は冷却
水人口、27は冷却水出口である。)との間に電圧を印
加し、アーク放電させ、アーク熱により原料2Oを溶融
した。
In this state, the tungsten electrode (-pole) inside the melting chamber 22
A voltage is applied between 24 and a water-cooled copper crucible (child) 25 (in the figure, 26 is the cooling water population, and 27 is the cooling water outlet), an arc is discharged, and the raw material 2O is melted by the arc heat. did.

その後、アーク放電を止めて、溶融物を冷却凝固させた
Thereafter, the arc discharge was stopped and the melt was allowed to cool and solidify.

得られた鋳塊を、ハンマーミルで粗粉砕後、アルミナボ
ールミルで微粉砕した後、分級し、粒径1〜5μmの複
合粉末を得た。この複合粉末を99%と、焼結助材とし
て粒径1〜5μmのY・2O31%を混合した後、スプ
レィドライヤを用いて造粒し、得られた造粒粉を、プレ
ス機により2,000kg/crn”の圧力を加えて圧
粉した。この圧粉体を、アルゴンガス雰囲気中で、15
00℃に2時間保持して常圧焼結し、直径60mm1厚
さ15mmの焼結体を作成した。
The obtained ingot was roughly pulverized with a hammer mill, finely pulverized with an alumina ball mill, and then classified to obtain a composite powder with a particle size of 1 to 5 μm. After mixing 99% of this composite powder and 31% of Y.2O with a particle size of 1 to 5 μm as a sintering aid, it was granulated using a spray dryer, and the resulting granulated powder was The powder was compacted by applying a pressure of 1,000 kg/crn.
The mixture was kept at 00° C. for 2 hours and sintered under normal pressure to produce a sintered body with a diameter of 60 mm and a thickness of 15 mm.

このような焼結方法により、実施例1と同様にしてビン
オンディスク試験片を作成し、同様に試験を行なった。
Using this sintering method, a bottle-on-disk test piece was prepared in the same manner as in Example 1, and the test was conducted in the same manner.

結果を第2表に示す。The results are shown in Table 2.

第  2  表 第2表より、実施例1.2の本発明の焼結体は共に比較
例1.2の焼結体より、耐摩耗性が著しく優れているこ
とが明らかである。
Table 2 From Table 2, it is clear that both the sintered bodies of the present invention of Example 1.2 have significantly better wear resistance than the sintered bodies of Comparative Example 1.2.

[発明の効果] 以上詳述した通り、本発明のCr2Os −M。[Effect of the invention] As detailed above, Cr2Os-M of the present invention.

系焼結体は、Cr2OaとMoが微細に分散し、良好な
潤滑剤の保持特性を有し、著しく耐摩耗性及び耐焼き付
き性に優れると共に、機械的特性に優れる高特性材料で
ある。
The system sintered body is a high-performance material in which Cr2Oa and Mo are finely dispersed, has good lubricant retention properties, has extremely excellent wear resistance and seizure resistance, and has excellent mechanical properties.

しかも、本発明のCr2Oa −Mo系焼結体は、焼結
により、あらゆる形状、大きさの部材に適用することが
でき、厚肉化による耐摩耗性の向上を図ることも可能で
ある。
Moreover, the Cr2Oa-Mo based sintered body of the present invention can be applied to members of all shapes and sizes by sintering, and it is also possible to improve wear resistance by increasing the thickness.

本発明によれば、潤滑剤を用いる摺動部材等の耐久性を
大幅に延長することが可能である。
According to the present invention, it is possible to significantly extend the durability of sliding members and the like that use lubricant.

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

第1図は本発明のCr 2O3  M O系焼結体の製
造方法を示す系統図、第2図は本発明のCr2O3−M
o系焼結体のMoとCr2Ogとの含有割合の好適値を
示すグラフ、第3図は実施例及び比較例で作製した試験
片の斜視図、第4図は同正面図、第5図は実施例及び比
較例の試験方法を説明する断面図、第6図は実施例2で
用いたアーク溶解炉を示す断面図である。 11・・・ディスク型試験片、 12・・・ピン型試験片、 2O・・・原料、 21・・・溶解炉、 24・・・タングステン電極、 25・・・銅坩堝。
FIG. 1 is a system diagram showing the method for producing a Cr2O3-M O-based sintered body of the present invention, and FIG.
A graph showing the preferred content ratio of Mo and Cr2Og in the o-based sintered body, FIG. 3 is a perspective view of the test pieces prepared in Examples and Comparative Examples, FIG. 4 is a front view of the same, and FIG. FIG. 6 is a cross-sectional view illustrating the test method of Examples and Comparative Examples, and FIG. 6 is a cross-sectional view showing the arc melting furnace used in Example 2. DESCRIPTION OF SYMBOLS 11... Disc-shaped test piece, 12... Pin-shaped test piece, 2O... Raw material, 21... Melting furnace, 24... Tungsten electrode, 25... Copper crucible.

Claims (1)

【特許請求の範囲】[Claims] (1)30〜90重量%のCr_2O_3と10〜70
重量%のMoとを含み、かつCr_2O_3とMoとの
合計が70〜100重量%であることを特徴とするCr
_2O_3−Mo系焼結体。
(1) 30-90% by weight of Cr_2O_3 and 10-70% by weight
Cr containing % by weight of Mo, and the total of Cr_2O_3 and Mo is 70 to 100% by weight.
_2O_3-Mo-based sintered body.
JP23820088A 1988-09-22 1988-09-22 Cr2o3-mo sintered body Pending JPH0288744A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23820088A JPH0288744A (en) 1988-09-22 1988-09-22 Cr2o3-mo sintered body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23820088A JPH0288744A (en) 1988-09-22 1988-09-22 Cr2o3-mo sintered body

Publications (1)

Publication Number Publication Date
JPH0288744A true JPH0288744A (en) 1990-03-28

Family

ID=17026643

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23820088A Pending JPH0288744A (en) 1988-09-22 1988-09-22 Cr2o3-mo sintered body

Country Status (1)

Country Link
JP (1) JPH0288744A (en)

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