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JPH06346077A - Sliding part - Google Patents

Sliding part

Info

Publication number
JPH06346077A
JPH06346077A JP13762493A JP13762493A JPH06346077A JP H06346077 A JPH06346077 A JP H06346077A JP 13762493 A JP13762493 A JP 13762493A JP 13762493 A JP13762493 A JP 13762493A JP H06346077 A JPH06346077 A JP H06346077A
Authority
JP
Japan
Prior art keywords
coating
film
wear
sliding
oxygen
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
JP13762493A
Other languages
Japanese (ja)
Other versions
JP2925430B2 (en
Inventor
Seiji Hasei
政治 長谷井
Uorufu Jiyooji
ウォルフ ジョージ
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 JP13762493A priority Critical patent/JP2925430B2/en
Publication of JPH06346077A publication Critical patent/JPH06346077A/en
Application granted granted Critical
Publication of JP2925430B2 publication Critical patent/JP2925430B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Sliding-Contact Bearings (AREA)
  • Lubricants (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

PURPOSE:To prepare a hard coating film composed mainly of Cr, having excellent sliding characteristics such as abrasion resistance and seizure resistance and exhibiting excellent initial conformability. CONSTITUTION:The sliding part is produced by coating a substrate with a coating film composed of Cr, an M group (M is Ti, V, Zr, Nb, Mo, Hf, Ta, W and/or Al), N and O and having a compositional ratio of the metallic elements M/(Cr+M) of 1-55 atom % and that of gaseous elements O/(N+O) of 5-80 atom %.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、摺動部に硬質皮膜を有
する、自動車部品やコンプレッサー部品などの機械部品
に用いられる摺動部材に関し、更に詳しく述べるなら
ば、クロムを主たる金属成分としさらに1種または2種
以上の金属元素と窒素及び酸素からなる皮膜を被覆した
摺動部材に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sliding member having a hard coating on the sliding portion and used for machine parts such as automobile parts and compressor parts. More specifically, chromium is the main metal component. The present invention relates to a sliding member coated with a film composed of one or more metal elements and nitrogen and oxygen.

【0002】[0002]

【従来の技術】自動車の内燃機関やコンプレッサーなど
の高回転化、高出力化等により機械部品などの摺動部
は、益々過酷な条件下での耐摩耗性、耐焼付性といった
摺動特性の向上が期待されている。また切削工具におい
ても切削速度増大により同様に摺動特性の向上が期待さ
れている。従来より摺動特性改善策として、硬質クロム
めっきによる耐摩耗性の改善、窒化またはモリブデン溶
射による耐焼付性の向上などの表面処理が挙げられる。
2. Description of the Related Art Sliding parts such as mechanical parts are subject to sliding characteristics such as wear resistance and seizure resistance under increasingly severe conditions due to higher rotation speed and higher output of internal combustion engines and compressors of automobiles. It is expected to improve. Similarly, in cutting tools, it is expected that the sliding characteristics will be improved by increasing the cutting speed. Conventionally, as a measure for improving sliding characteristics, surface treatment such as improvement of wear resistance by hard chrome plating and improvement of seizure resistance by nitriding or molybdenum spraying can be mentioned.

【0003】しかしながら、これらの方法では摺動材料
としての十分な摺動特性が得られず、最近物理的気相蒸
着(PVD)法あるいは化学気相析出(CVD)法によ
り化学的にも比較的安定なCr−N系、Ti−N系硬質
皮膜を作製する方法が検討されている。ところがCr−
N系皮膜は、皮膜硬さが比較的低いため、皮膜の摩耗が
起こりやすく、この点の改良は試みられているもののい
まだ十分な摺動特性は得られていない。
However, these methods do not provide sufficient sliding properties as a sliding material, and have recently been relatively chemically chemically prepared by physical vapor deposition (PVD) or chemical vapor deposition (CVD). Methods for producing stable Cr-N-based and Ti-N-based hard coatings have been investigated. However, Cr-
Since the N-based coating has a relatively low coating hardness, the coating is apt to wear, and although attempts have been made to improve this point, sufficient sliding characteristics have not yet been obtained.

【0004】そこで、さらに皮膜硬さが高く、摺動特性
に優れた皮膜の開発が望まれ、Ti−N系皮膜が注目さ
れている。しかしながらTi−N系皮膜は、機械部品な
どの摺動部材として利用する場合には皮膜硬さが高すぎ
て相手材を摩耗させてしまうという欠点があり、また皮
膜と接する相手材との「初期なじみ」が悪い欠点もあ
る。ここで「初期なじみ」とは、機械加工または成膜自
体に起因する粗さをもつ摺動部材の表面が摺動開始後の
短時間の内に相手材と摺動接触し表面が微小且つ平滑に
摩耗する結果、接触面積を増加させることにより接触面
圧を低減させて、潤滑油膜切れを起こし難くし、以って
摩耗や焼き付きの発生を防ぐ性能である。Ti−N系皮
膜のような皮膜硬さの高すぎる皮膜を被覆した摺動部材
は、初期なじみが悪いことにより、摺動初期において摩
耗や焼付現象を起こしやすいという問題があった。
Therefore, it is desired to develop a film having higher film hardness and excellent sliding characteristics, and a Ti-N-based film has attracted attention. However, the Ti-N-based coating has a drawback that the hardness of the coating is too high when it is used as a sliding member such as a machine part, and it causes abrasion of the mating material. "Familiarity" also has the disadvantage. Here, "initial familiarity" means that the surface of the sliding member, which has roughness caused by machining or film formation itself, comes into sliding contact with the mating material within a short time after the start of sliding, and the surface is minute and smooth. As a result of abrasion, the contact surface pressure is reduced by increasing the contact area, making it difficult for lubricant oil film breakage to occur, thereby preventing wear and seizure. A sliding member coated with a film having a too high film hardness such as a Ti-N-based film has a problem that it is likely to cause abrasion or seizure at the initial sliding stage due to poor initial fitting.

【0005】[0005]

【発明が解決しようとする課題】本発明は、上記の点に
鑑みて、Crを主たる金属成分とする皮膜を被覆した摺
動材料において、耐摩耗性および耐焼付性等の摺動特性
に優れ、初期なじみが良好な硬質皮膜を被覆することに
より上記の問題を解決することを目的とする。さらに、
本出願人は上記の問題点を解決するために特願平5−1
20062号において、クロム、M群(M;チタン、バ
ナジウム、ジルコニウム、ニオブ、モリブデン、ハフニ
ウム、タンタル、タングステン及びアルミニウムから選
択された1種または2種以上の金属元素)、及び窒素か
らなり、金属元素の組成比が原子%比でM/(Cr+
M)=1〜55%である皮膜を被覆した摺動部材を提案
したが、この発明においてはさらに上記の耐摩耗性を改
良するとともに相手材の摩耗を少なくすることを目的と
する。
In view of the above points, the present invention provides a sliding material coated with a film containing Cr as a main metal component, which has excellent sliding characteristics such as wear resistance and seizure resistance. The object of the present invention is to solve the above problems by coating a hard film having good initial familiarity. further,
In order to solve the above problems, the present applicant has filed Japanese Patent Application No. 5-1
No. 20062, a metal element consisting of chromium, an M group (M; one or more metal elements selected from titanium, vanadium, zirconium, niobium, molybdenum, hafnium, tantalum, tungsten and aluminum) and nitrogen, The composition ratio of M / (Cr +
Although a sliding member coated with a film of M) = 1 to 55% was proposed, the present invention aims to further improve the above-mentioned wear resistance and reduce the wear of the mating member.

【0006】[0006]

【課題を解決するための手段】すなわち、本発明に係わ
る摺動部材は、クロム、M群(M;チタン、バナジウ
ム、ジルコニウム、ニオブ、モリブデン、ハフニウム、
タンタル、タングステン及びアルミニウムから選択され
た1種または2種以上の金属元素)、窒素及び酸素から
なり、金属元素の組成比が原子%比でM/(Cr+M)
=1〜55%であり、かつガス元素の組成比が原子%比
でO/(N+O)=5〜80%である皮膜を基体に被覆
したことを特徴とする。この皮膜は、CrNあるいはC
r2 NにM群の元素及び酸素を添加することにより、皮
膜の硬さ自体はCrNあるいはCr2 N皮膜よりも高
く、耐摩耗性及び耐焼付性並びに初期なじみ性をCrN
あるいはCr2 NG皮膜よりも良好にしたものである。
M群の元素及び酸素の作用について述べると、(イ)何
れもCrNあるいはCr2 N皮膜の硬度を増加させる
が、前者の方が硬度増加の割合が大であり、(ロ)前者
はCrNあるいはCr2 N皮膜の摩擦係数をやや増加さ
せるものの、後者はこれを大幅に減少させ、(ハ)何れ
もCrNあるいはCr2 N皮膜のオイル中での腐食によ
る減量を抑制するが、前者の方が抑制程度が大である。
このような物性に対する影響でM群の元素と酸素では異
なるので、それぞれ別の群に分け、またTi,V,Z
r,Nb,Mo,Hf,Ta,W,Alはいずれも上記
の点で共通であるので、一つの群に含めることとした。
[Means for Solving the Problems] That is, the sliding member according to the present invention comprises chromium, group M (M; titanium, vanadium, zirconium, niobium, molybdenum, hafnium,
One or more metal elements selected from tantalum, tungsten and aluminum), nitrogen and oxygen, and the composition ratio of the metal elements is M / (Cr + M) in atomic% ratio.
= 1 to 55%, and the composition ratio of the gas elements is O / (N + O) = 5 to 80% in atomic% ratio. This film is CrN or C
By adding an element of group M and oxygen to r2 N, the hardness of the coating itself is higher than that of CrN or Cr2 N coating, and the wear resistance, seizure resistance and initial familiarity of CrN are improved.
Alternatively, it is better than the Cr2 NG coating.
The effects of the elements of group M and oxygen are as follows: (a) Both increase the hardness of the CrN or Cr2N film, but the former has a higher rate of increase in hardness, and (b) the former is CrN or Cr2. Although the coefficient of friction of the N film is slightly increased, the latter greatly reduces it, and (c) both suppress the reduction of CrN or Cr2 N film due to corrosion in oil, but the former is less effective. Is large.
Since the elements of group M and oxygen are different due to the influence on the physical properties, they are divided into different groups, and Ti, V, Z
Since r, Nb, Mo, Hf, Ta, W, and Al are all common in the above points, they are included in one group.

【0007】ここでM/(Cr+M)の金属元素組成比
が1%未満であると耐摩耗性向上の効果が少なく、一方
55%を超えると耐焼付性及び初期なじみの向上が図れ
ないために、金属元素組成比は1〜55%の範囲とし
た。ガス元素の組成比O/(N+O)が5%未満である
と相手材の摩耗が多くなり、一方80%を越えると皮膜
自体の摩耗が多くなり摺動特性の向上は図れなかった。
If the metal element composition ratio of M / (Cr + M) is less than 1%, the effect of improving wear resistance is small, whereas if it exceeds 55%, seizure resistance and initial familiarity cannot be improved. The metal element composition ratio was in the range of 1 to 55%. If the composition ratio O / (N + O) of the gas element is less than 5%, the wear of the mating material increases, whereas if it exceeds 80%, the wear of the coating itself increases and the sliding characteristics cannot be improved.

【0008】基体としてはFe系、Al系、Ti系等の
各種材料を使用することができる。Cr−M−N−O系
皮膜の厚さは特に制限が無いが、1〜50μmの範囲内
であることが好ましい。同じく皮膜粗さはRaで1μm
以下であることが好ましい。
As the base material, various materials such as Fe-based material, Al-based material and Ti-based material can be used. The thickness of the Cr-M-N-O-based coating is not particularly limited, but is preferably in the range of 1 to 50 μm. Similarly, the film roughness Ra is 1 μm
The following is preferable.

【0009】さらに、相手材としては特に制限がなく鋳
鉄もしくは鋼材、Crめっきを施したこれらの材料、溶
射皮膜付材料などが使用可能である。また、本発明の皮
膜は十分に清浄化された基体上にPVD又はCVD好ま
しくはPVDで成膜されるものである。
Further, the mating material is not particularly limited, and cast iron or steel material, these materials plated with Cr, materials having a thermal spray coating, etc. can be used. Further, the coating film of the present invention is formed by PVD or CVD, preferably PVD, on a sufficiently cleaned substrate.

【0010】[0010]

【作用】CrN系皮膜は耐摩耗性が低く、一方TiN系
皮膜は初期なじみ性が悪いために、いずれも焼き付きを
起こしやすいが、Crと他の金属元素M、N及びOを共
存させたCr−M−N−O系皮膜とすることにより焼付
が発生し難くなった。また耐摩耗性が良好になることに
よりなじみが実現した以降の摩耗は少なくなり、さらに
相手材の摩耗も減少した。以下、金属元素(M)として
Vを選んだ実施例により本発明を詳しく説明する。
[Function] The CrN-based coating has low wear resistance, while the TiN-based coating has poor initial conformability, and thus both are prone to seizure. However, Cr containing Cr and other metal elements M, N and O coexist. By using a -M-N-O type coating, it became difficult for seizure to occur. In addition, since the wear resistance is improved, the wear after the fitting is realized is reduced and the wear of the mating material is also reduced. Hereinafter, the present invention will be described in detail with reference to examples in which V is selected as the metal element (M).

【0011】[0011]

【実施例】本実施例で使用した皮膜形成の基体は高クロ
ム鋼(JIS規格SUJ−2)である。基体はあらかじ
めフロン液中で超音波洗浄を行い、鏡面仕上げされた基
体表面に以下に説明する手順で陰極アークプラズマ式イ
オンプレーティングによりCr−N系硬質皮膜(比較
例)、Cr−V−N系硬質皮膜(比較例)及びCr−V
−N−O系硬質皮膜(実施例)を形成した。
EXAMPLE The film-forming substrate used in this example is high chromium steel (JIS standard SUJ-2). The substrate was ultrasonically cleaned in a Freon solution in advance, and the mirror-finished substrate surface was subjected to cathodic arc plasma ion plating according to the procedure described below to perform Cr-N hard coating (comparative example), Cr-VN. System hard coating (comparative example) and Cr-V
A -NO hard coating (Example) was formed.

【0012】超音波洗浄された基体をイオンプレーティ
ング装置の真空容器(チャンバ)内に取り付け、続いて
チャンバ内圧力が1.3×10-3Pa(パスカル)とな
るまで真空引きを行った。この真空度が達成された時点
から、チャンバ内に内蔵されているヒーターにより基体
を300〜600℃まで加熱して、基体表面に付着ある
いは吸着しているガス成分を放出させ、その後200℃
まで冷却した。
The ultrasonically cleaned substrate was mounted in a vacuum container (chamber) of an ion plating apparatus, and then vacuumed until the chamber pressure reached 1.3 × 10 −3 Pa (pascal). From the time when this degree of vacuum is achieved, the substrate is heated to 300 to 600 ° C. by the heater built in the chamber to release the gas components adhering to or adsorbing on the substrate surface, and then 200 ° C.
Cooled down.

【0013】チャンバ内圧力が4×10-3Pa以下とな
った時点で、陰極とした各種組成のCr−V合金ターゲ
ットの表面でアーク放電を発生させ、CrおよびVの大
部分がイオン化された状態でターゲット表面から飛出さ
せた。
When the pressure in the chamber becomes 4 × 10 -3 Pa or less, arc discharge is generated on the surface of the Cr-V alloy target having various compositions used as the cathode, and most of Cr and V are ionized. It was ejected from the target surface.

【0014】この時基体を装着した治具には−700〜
−1000Vのバイアス電圧を印加しておき、ターゲッ
トから飛び出すイオン化したCrおよびVを基体と治具
の表面に吸引し、さらにこれらのイオンを高速で被処理
面に衝突させた。このようなイオン化した金属の衝突に
より被処理面の酸化物などを削るいわゆるスパッタクリ
ーニングにより基体表面の活性化処理を行った。
At this time, the jig on which the base body is mounted is -700 to
A bias voltage of -1000 V was applied, the ionized Cr and V jumping from the target were attracted to the surfaces of the substrate and the jig, and these ions were made to collide with the surface to be processed at high speed. The activation treatment of the substrate surface was performed by so-called sputter cleaning in which oxides and the like on the surface to be treated were scraped by the collision of the ionized metal.

【0015】その後、アーク放電が起こっているチャン
バ中に少量の窒素ガスを導入することにより一部のイオ
ン化したCrおよびVは、窒素ガスと結合し基体表面に
窒化物皮膜となって析出した。その後、さらに窒素ガス
流量を増やし所定のガス元素ガス元素の組成比となる流
量の酸素ガスを導入して0.7〜4.0Pa程度の圧力
とし、また0〜−100Vのバイアス電圧を基体に印加
して基体表面にCr−V−N−O系硬質皮膜を1〜50
μmの厚さに形成させた。なお、比較例のCr−V−N
系皮膜形成の場合は酸素ガスの導入をせずに同様に成膜
を行った。所定膜厚形成後、チャンバ内温度が150℃
以下になるまで冷却してから、膜被覆された基体をチャ
ンバ外に取り出した。皮膜の硬度はHv=1000〜2
500の範囲であった。
After that, a small amount of nitrogen gas was introduced into the chamber where the arc discharge occurred, and a part of ionized Cr and V were combined with the nitrogen gas and deposited as a nitride film on the surface of the substrate. Thereafter, the flow rate of nitrogen gas is further increased to introduce oxygen gas at a flow rate that provides a predetermined gas element gas element composition ratio to a pressure of about 0.7 to 4.0 Pa, and a bias voltage of 0 to -100 V is applied to the substrate. Apply 1-50 Cr-VNO hard coating on the substrate surface by applying
It was formed to a thickness of μm. In addition, Cr-VN of the comparative example
In the case of forming a system film, the film was similarly formed without introducing oxygen gas. After forming the specified film thickness, the chamber temperature is 150 ℃
After cooling to the following, the film-coated substrate was taken out of the chamber. The hardness of the film is Hv = 1000-2
It was in the range of 500.

【0016】上記方法により得られた皮膜を用いて、摺
動試験を行った。 実施例2 ねずみ鋳鉄(FC25)を相手材としてピンオンディス
ク型摩擦試験機によりスカッフ試験を行った。スカッフ
試験条件は、以下の通りであった。 潤滑方法:モーターオイル#30、油温80℃、油量4
cc/sec 摩擦速度:8m/sec 接触荷重:初期2MPaから1MPaごとに焼付まで増
加させる。 摩擦時間:各荷重で180sec保持 表1にスカッフ試験結果を示す。
A sliding test was carried out using the film obtained by the above method. Example 2 A scuff test was carried out by a pin-on-disc type friction tester using gray cast iron (FC25) as a counterpart material. The scuff test conditions were as follows. Lubrication method: Motor oil # 30, oil temperature 80 ° C, oil amount 4
cc / sec Friction speed: 8 m / sec Contact load: Initially increased from 2 MPa to seizure every 1 MPa. Friction time: Hold for 180 seconds under each load Table 1 shows the results of the scuff test.

【0017】[0017]

【表1】 No V(Cr +V)-1 O(N +O )-1 スカッフ値 本 1 Cr−V −N −O 15 20 2.1 発 2 Cr−V −N −O 50 20 2.3 明 3 Cr−V −N −O 50 70 2.4 比 1 Cr−V −N 50 0 2.0 較 2 Cr−N 0 0 1.0 スカッフ値は、比較対象であるCr−Nを1.0とした時の値である。[Table 1] No V (Cr + V) -1 O (N + O) -1 Scuff value 1 Cr-V -N -O 15 20 2.1 shot 2 Cr-V -N -O 50 20 2.3 Clear 3 Cr-V -N-O50 70 2.4 Ratio 1 Cr-V -N 50 0 2.0 Comparison 2 Cr-N 0 0 1.0 The scuff value is the value when the comparison target Cr-N is 1.0.

【0018】本発明によるNo.1,2および3のCr
−V−N−O系皮膜は、皮膜中の金属元素に対するV原
子%(以後、単に「V原子%」と称す)がそれぞれ1
5、50および50%であり、皮膜中の窒素原子と酸素
原子の和に対する酸素原子%(以後、単に「酸素原子
%」と称する)がそれぞれ、20、20および70%で
ある。金属原子とガス原子の割合(比率)はほぼ(2〜
1):1とすることが望ましいが、この限りではない。
No. 1 according to the present invention. 1, 2 and 3 Cr
The -V-N-O-based film has a V atom% (hereinafter simply referred to as "V atom%") of 1 with respect to the metal element in the film.
5, 50 and 50%, and the oxygen atom% (hereinafter simply referred to as "oxygen atom%") with respect to the sum of nitrogen atoms and oxygen atoms in the film is 20, 20 and 70%, respectively. The ratio (ratio) of metal atoms and gas atoms is approximately (2 to
1): It is desirable to set it to 1: but it is not limited to this.

【0019】皮膜中のV原子%と酸素原子%が皮膜の特
性に及ぼす影響を調べた。比較例としてVを含まないC
r−N系皮膜について同じ条件でスカッフ試験を行い得
られたスカッフ値(焼付面圧)1.0に対して、本発明
のNo.1、2及び3のCr−V−N−O系皮膜ではス
カッフ値が約2倍以上向上した。さらに、No.2とN
o.3のCr−V−N−O系皮膜を比較すると、酸素原
子%大きいNo.3が高いスカッフ値を示した。
The effect of V atomic% and oxygen atomic% in the coating on the characteristics of the coating was investigated. C that does not include V as a comparative example
A scuff value (baking surface pressure) of 1.0 was obtained by performing a scuff test on the r-N type coating under the same conditions. The scuff value of the Cr-V-N-O-based coatings of 1, 2 and 3 was improved by about two times or more. Furthermore, No. 2 and N
o. Comparing the Cr-V-N-O-based coatings of No. 3 with No. 3 having a large oxygen atom%. 3 showed a high scuff value.

【0020】実施例3 ピン−ドラム式摩耗試験機により、ドラムにねずみ鋳鉄
(FC25)を用いて摩耗試験を行った。摩耗試験条件
は以下の通りであった。 潤滑方法:モーターオイル#30、油温80℃、油量8
cc/sec ドラム回転速度:5m/sec 接触荷重:1.5MPa 試験時間:30ksec 表2に摩耗試験結果を示す。
Example 3 A pin-drum abrasion tester was used to perform an abrasion test using gray cast iron (FC25) for the drum. The wear test conditions were as follows. Lubrication method: Motor oil # 30, oil temperature 80 ° C, oil amount 8
cc / sec Drum rotation speed: 5 m / sec Contact load: 1.5 MPa Test time: 30 ksec Table 2 shows the wear test results.

【0021】[0021]

【表2】 ピン ドラム No V(Cr +V)-1 O(N +O )-1 摩耗量 摩耗量 本 1 Cr−V −N −O 15 20 0.5 0.7 発 2 Cr−V −N −O 50 20 0.4 0.6 明 3 Cr−V −N −O 50 70 0.4 0.6 比 1 Cr−V −N 50 0 0.6 0.8 較 2 Cr−N 0 0 1.0 1.0 スカッフ値は、比較対象であるCr−Nを1.0とした時の値である。[Table 2] Pin drum No V (Cr + V) -1 O (N + O) -1 Abrasion amount Abrasion amount 1 Cr-V-N-O 15 20 0.5 0.7 Shot 2 Cr-V-N-O 50 20 0.4 0.6 Bright 3 Cr-V -N -O 50 70 0.4 0.6 Ratio 1 Cr-V -N 50 0 0.6 0.8 Comparison 2 Cr-N 0 0 1.0 1.0 The scuff value is 1.0 for Cr-N which is the comparison target. It is the value at the time of doing.

【0022】比較対象として、V及び酸素を含まないC
r−N系皮膜及び酸素を含まないCr−V−N皮膜につ
いてCr−V−N−O皮膜と同じ条件で摩耗試験を行っ
た。ここで、皮膜を被覆したピンの摩耗量は摩耗した接
触面のドラム回転方向の幅、ドラムの摩耗量はドラムの
摩耗深さより求めた。Cr−N系皮膜の場合のピン摩耗
量及びドラム摩耗量をそれぞれ1.0としてそれぞれの
特性を表2に示す。
As a comparison object, V and C containing no oxygen
A wear test was performed on the r-N-based coating and the Cr-VN coating containing no oxygen under the same conditions as the Cr-VN-O coating. Here, the amount of wear of the pin coated with the film was obtained from the width of the worn contact surface in the drum rotation direction, and the amount of wear of the drum was obtained from the wear depth of the drum. Table 2 shows the respective characteristics when the amount of pin wear and the amount of drum wear in the case of the Cr-N type coating are 1.0.

【0023】本発明によるCr−V−N−0系皮膜は、
ドラム摩耗量が比較例に比べてやや低減しており、一方
ピンの摩耗量は比較例に比べ著しく低減している。特
に、No.2,No.3のCr−V−N−O系皮膜で
は、Cr−N系皮膜の約1/2,Cr−V−N系皮膜の
2/3の摩耗量に抑えられている。
The Cr-VN-0 type coating according to the present invention comprises
The amount of wear of the drum is slightly reduced as compared with the comparative example, while the amount of wear of the pin is significantly reduced as compared with the comparative example. In particular, No. 2, No. In the Cr-V-N-O-based coating of No. 3, the wear amount is suppressed to about 1/2 of the Cr-N-based coating and 2/3 of the Cr-VN-based coating.

【0024】以上のスカッフ試験および摩耗試験の結果
から、Cr−N系皮膜及びCr−V−N皮膜に比べCr
−V−N−O系皮膜は、耐焼付性に優れ、初期なじみが
良好で、摺動部相手材の摩耗を抑えられる皮膜であるこ
とがわかった。
From the results of the above scuffing test and abrasion test, it is possible to compare the Cr-N type coating and the Cr-VN coating with Cr.
It has been found that the -V-N-O type coating has excellent seizure resistance, good initial familiarity, and can suppress wear of the mating material of the sliding portion.

【0025】[0025]

【発明の効果】以上のように、摺動面に主たる金属成分
であるCr,他の金属元素、窒素及び酸素からなる皮膜
を被覆することにより、従来のCr−N系又はCr−V
−N皮膜を被覆するよりも相手材を摩耗させることがな
く、初期なじみが良好で、耐摩耗性および耐焼付性等の
摺動特性に優れた摺動部材が得られる。
As described above, the conventional Cr-N system or Cr-V system is formed by coating the sliding surface with a film composed of Cr, which is the main metal component, other metal elements, nitrogen and oxygen.
It is possible to obtain a sliding member that does not wear the mating material more than the case where the -N film is coated, has good initial conformability, and has excellent sliding characteristics such as wear resistance and seizure resistance.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C10N 10:08 10:10 10:12 30:06 30:08 40:02 50:08 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area C10N 10:08 10:10 10:12 30:06 30:08 40:02 50:08

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 クロム、M群(M;チタン、バナジウ
ム、ジルコニウム、ニオブ、モリブデン、ハフニウム、
タンタル、タングステン及びアルミニウムから選択され
た1種または2種以上の金属元素)、窒素及び酸素から
なり、金属元素の組成比が原子%比でM/(Cr+M)
=1〜55%であり、かつガス元素の組成比が原子%比
O/(N+O)=5〜80%である皮膜を基体に被覆し
たことを特徴とする摺動部材。
1. Chromium, group M (M; titanium, vanadium, zirconium, niobium, molybdenum, hafnium,
One or more metal elements selected from tantalum, tungsten and aluminum), nitrogen and oxygen, and the composition ratio of the metal elements is M / (Cr + M) in atomic% ratio.
= 1 to 55%, and the composition ratio of the gas element is atomic% ratio O / (N + O) = 5 to 80%.
JP13762493A 1993-06-08 1993-06-08 Sliding member Expired - Fee Related JP2925430B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13762493A JP2925430B2 (en) 1993-06-08 1993-06-08 Sliding member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13762493A JP2925430B2 (en) 1993-06-08 1993-06-08 Sliding member

Publications (2)

Publication Number Publication Date
JPH06346077A true JPH06346077A (en) 1994-12-20
JP2925430B2 JP2925430B2 (en) 1999-07-28

Family

ID=15203019

Family Applications (1)

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Cited By (7)

* Cited by examiner, † Cited by third party
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US6060182A (en) * 1997-06-09 2000-05-09 Teikoku Piston Ring Co., Ltd. Hard coating material, sliding member covered with hard coating material and manufacturing method thereof
EP1132498A1 (en) * 2000-03-09 2001-09-12 METAPLAS IONON Oberflächenveredelungstechnik GmbH Hard layer coated parts
EP1087031A3 (en) * 1999-09-24 2002-06-12 Teikoku Piston Ring Co., LTd. Hard film, sliding member covered with hard film and manufacturing method thereof
JP2004522108A (en) * 2001-06-07 2004-07-22 イスパノ・シユイザ Sliding bearing with friction film and manufacturing method thereof
US6794064B2 (en) * 2001-11-28 2004-09-21 Metaplas Ionon Oberflaechenveredelungstechnik Gmbh Hard coating coated parts
JP2007170467A (en) * 2005-12-20 2007-07-05 Teikoku Piston Ring Co Ltd piston ring
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Publication number Priority date Publication date Assignee Title
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6060182A (en) * 1997-06-09 2000-05-09 Teikoku Piston Ring Co., Ltd. Hard coating material, sliding member covered with hard coating material and manufacturing method thereof
EP1087031A3 (en) * 1999-09-24 2002-06-12 Teikoku Piston Ring Co., LTd. Hard film, sliding member covered with hard film and manufacturing method thereof
EP1132498A1 (en) * 2000-03-09 2001-09-12 METAPLAS IONON Oberflächenveredelungstechnik GmbH Hard layer coated parts
US6730392B2 (en) 2000-03-09 2004-05-04 Metaplas Ionon Oberflächenveredelungstechnik GmbH Hard layer coated parts
JP2004522108A (en) * 2001-06-07 2004-07-22 イスパノ・シユイザ Sliding bearing with friction film and manufacturing method thereof
US6794064B2 (en) * 2001-11-28 2004-09-21 Metaplas Ionon Oberflaechenveredelungstechnik Gmbh Hard coating coated parts
JP2007170467A (en) * 2005-12-20 2007-07-05 Teikoku Piston Ring Co Ltd piston ring
WO2014155632A1 (en) * 2013-03-28 2014-10-02 オーエスジー株式会社 Hard film for tools, production method therefor, and hard film-coated metal machining tool
JP5995029B2 (en) * 2013-03-28 2016-09-28 オーエスジー株式会社 Hard coating for tool, manufacturing method thereof, and hard coating coated metal working tool

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