JPH06330347A - Sliding member - Google Patents

Sliding member

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Publication number
JPH06330347A
JPH06330347A JP12006193A JP12006193A JPH06330347A JP H06330347 A JPH06330347 A JP H06330347A JP 12006193 A JP12006193 A JP 12006193A JP 12006193 A JP12006193 A JP 12006193A JP H06330347 A JPH06330347 A JP H06330347A
Authority
JP
Japan
Prior art keywords
coating
wear
film
sliding
sliding member
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
JP12006193A
Other languages
Japanese (ja)
Other versions
JP3256024B2 (en
Inventor
Uorufu Jiyooji
ウォルフ ジョージ
Seiji Hasei
政治 長谷井
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 JP12006193A priority Critical patent/JP3256024B2/en
Publication of JPH06330347A publication Critical patent/JPH06330347A/en
Application granted granted Critical
Publication of JP3256024B2 publication Critical patent/JP3256024B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To provide a sliding member excellent in wear and seizing resistance by forming the coating film of a sliding member with metallic elements such as Ti and Cr and N and specifying the compsn. ratio between the metallic elements. CONSTITUTION:A coating film is formed with Ti, M (M is one or more kinds of metallic elements selected from among Cr, V, Zr, Nb, Mo, Hf, Ta, W and Al) and N. The compsn. ratio between the metallic elements is allowed to satisfy M/(Ti+M)=1-45 atomic %. A substrate is coated with this coating film to obtain the objective sliding member having satisfactory initial fitness and excellent in sliding characteristics.

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、
チタンを主たる金属成分としさらに1種または2種以上
の金属元素からなる窒化物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 used for a machine part such as an automobile part or a compressor part having a hard coating on a sliding part.
The present invention relates to a sliding member having titanium as a main metal component and a nitride film made of one or more metal elements.

【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、皮膜硬度が比較的低いため、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 likely 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、Ti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。
In view of the above points, the present invention provides a sliding material coated with a film containing Ti 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.

【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、チタン、とM群(M;クロム、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)及び窒素からなる皮
膜を基体に被覆した材料であることを特徴とする。この
皮膜は、M群の元素を添加することにより、皮膜の硬さ
自体はTiN皮膜よりも低いにもかかわらず、耐摩耗性
及び耐焼付性並びに初期なじみ性をTiN皮膜よりも良
好にしたものである。ここでM/(Ti+M)の金属元
素組成比が1%未満であると初期なじみ向上の効果が少
なく、一方45%を超えると耐焼付性の向上が図れない
ために、金属元素組成比は1〜45%の範囲とした。
[Means for Solving the Problems] That is, the sliding member according to the present invention is made of titanium, an M group (M; chromium, vanadium, zirconium, niobium, molybdenum, hafnium,
It is characterized by being a material in which a substrate is coated with a film composed of one or more kinds of metal elements selected from tantalum, tungsten and aluminum) and nitrogen. This coating has improved wear resistance, seizure resistance, and initial running-in property than the TiN coating, even though the hardness of the coating itself is lower than that of the TiN coating by adding the elements of group M. Is. Here, when the metal element composition ratio of M / (Ti + M) is less than 1%, the effect of improving the initial running-in is small, and when it exceeds 45%, the seizure resistance cannot be improved, so that the metal element composition ratio is 1%. The range was up to 45%.

【0007】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。Ti−M−N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 Ti-M-N-based coating is not particularly limited, but is preferably in the range of 1 to 50 μm. Similarly, the film roughness Ra is preferably 1 μm or less.

【0008】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.

【0009】[0009]

【作用】TiN系皮膜は初期なじみ性が悪く、一方Cr
N皮膜は耐摩耗性が低いために、いずれも焼き付きを起
こしやすいが、Tiと他の金属元素Mを共存させたTi
−M−N系皮膜とすることにより焼付が発生し難くなっ
た。また初期なじみ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った。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 TiN-based coating has poor initial conformability, while Cr
Since the N film has low wear resistance, it easily causes seizure, but Ti containing Ti and another metal element M coexists.
By using the -MN type coating, it became difficult for seizure to occur. In addition, since the initial familiarity was good, the wear after the familiarization was realized was reduced. Hereinafter, the present invention will be described in detail with reference to examples in which V is selected as the metal element (M).

【0010】[0010]

【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Ti−V−N系硬質皮膜を形
成した。
EXAMPLE The film-forming substrate used in this example is high chromium steel (JIS standard SUJ-2). The substrate was previously subjected to ultrasonic cleaning in a flon solution, and a Ti-VN hard coating was formed on the mirror-finished substrate surface by cathode arc plasma ion plating according to the procedure described below.

【0011】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 pressure in the chamber 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.

【0012】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Ti−V合金ターゲ
ットの表面でアーク放電を発生させ、Ti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 Ti-V alloy target having various compositions used as the cathode, and most of Ti and V are ionized. It was ejected from the target surface.

【0013】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Ti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, ionized Ti and V jumping from the target were attracted to the surfaces of the substrate and 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.

【0014】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Ti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Ti−V−N系硬質皮膜を1〜50μmの厚さに
形成させた。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=1500〜
2500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 Ti 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 a pressure of about 0.7 to 4.0 Pa, and a bias voltage of 0 to -100 V is applied to the substrate to form a Ti-VN hard coating on the substrate surface of 1 to 50 μm. Was formed to a thickness of. After forming a predetermined film thickness, the chamber temperature is 150
After cooling to below ℃, the film-coated substrate was taken out of the chamber. The hardness of the film is Hv = 1500
It was in the range of 2500.

【0015】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.

【0016】[0016]

【表1】 No. V/(Ti+V) スカッフ値 本 1 Ti−V−N 13 1.2 発 2 Ti−V−N 28 1.6 明 3 Ti−V−N 45 1.8 比 Ti−N 0 1.0 スカッフ値は、比較対象であるTi−Nを1.0とした
時の値である。
[Table 1] No. V / (Ti + V) scuff values present 1 Ti-V-N 13 1.2 rounds 2 Ti-V-N 28 1.6 Description 3 Ti-V-N 45 1.8 ratio Ti-N 0 1.0 compare scuff The value is a value when Ti-N to be compared is set to 1.0.

【0017】本発明によるNo.1,2および3のTi
−V−N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13、2
8および45%であった。比較例としてVを含まないT
i−N系皮膜について同じ条件でスカッフ試験を行っ
た。Ti−N系皮膜のスカッフ値(焼付面圧)1.0に
対して、No.1のTi−V−N系皮膜ではスカッフ値
が1.2と向上した。さらにV原子%を高くするにした
がってスカッフ値は向上し、V原子%が45%のTi−
V−N系皮膜では、Ti−N系皮膜の2倍近いスカッフ
値を示した。
No. 1 according to the present invention. 1, 2 and 3 Ti
-V-N system coating is V atom% to the metal element in the coating.
(Hereinafter, simply referred to as “V atom%”) is 13, 2 respectively
8 and 45%. As a comparative example, T containing no V
A scuffing test was performed on the iN coating under the same conditions. For the scuff value (baking surface pressure) of the Ti-N-based coating of 1.0, No. In the Ti-VN coating of No. 1, the scuff value was improved to 1.2. Further, as the V atom% is increased, the scuff value is improved, and the V atom% is 45% Ti-.
The VN-based coating showed a scuff value almost twice that of the Ti-N-based coating.

【0018】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 type 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.

【0019】[0019]

【表2】 No. V/(Ti+V) ピン摩耗量 ドラム摩耗量 本 1 Ti−V−N 13 0.8 0.9 発 2 Ti−V−N 28 0.9 0.7 明 3 Ti−V−N 45 0.9 0.6 比 Ti−N 0 1.0 1.0 ピン摩耗量およびドラム摩耗量は、比較対象であるTi
−Nを1.0とした時の値である。
[Table 2] No. V / (Ti + V) Pin wear amount Drum wear amount Main 1 Ti-V-N 13 0.8 0.9 Shot 2 Ti-V-N 28 0.9 0.7 Bright 3 Ti-V-N 45 0.9 0.6 ratio Ti-N 0 1.0 1.0 compare pin wear amount and drum wear amount is compared Ti
It is a value when -N is set to 1.0.

【0020】本発明によるTi−V−N系皮膜(No.
1、2および3)は、皮膜中のV原子%がそれぞれ1
3、28および45%であった。比較例としてVを含ま
ないTi−N系皮膜について同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。ピンの摩耗量に着目すると、Ti
−N系皮膜に比べTi−V−N系皮膜は、やや摩耗量が
低減している。一方ドラムの摩耗量に着目すると、Ti
−N系皮膜の場合に比べTi−V−N系皮膜の場合には
摩耗量が著しく低減し、V原子%が45%のTi−V−
N系皮膜では、Ti−N系皮膜の半分近い摩耗量に抑え
られている。
The Ti-VN coating according to the present invention (No.
1, 2 and 3) have a V atomic% of 1 in the coating, respectively.
3, 28 and 45%. As a comparative example, a wear test was conducted under the same conditions for a Ti-N-based coating containing no V. 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. Focusing on the amount of pin wear, Ti
The amount of wear of the Ti-VN-based coating is slightly reduced as compared with the -N-based coating. On the other hand, focusing on the amount of wear of the drum, Ti
In the case of Ti-VN coating, the amount of wear is remarkably reduced as compared with the case of -N coating, and Ti-V- with V atom% of 45% is used.
With the N-based coating, the amount of wear is suppressed to nearly half that of the Ti-N-based coating.

【0021】以上のスカッフ試験および摩耗試験の結果
から、Ti−N系皮膜に比べTi−V−N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 scuff test and wear test, the Ti-VN coating is superior to the Ti-N coating in seizure resistance, has good initial familiarity, and wears the mating material of the sliding portion. It turned out to be a film that can be suppressed.

【0022】[0022]

【発明の効果】以上のように、摺動面にTiを主たる金
属成分としさらに他の金属元素を含む窒化物皮膜を被覆
することにより、従来のTi−N系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。
INDUSTRIAL APPLICABILITY As described above, by coating the sliding surface with the nitride film containing Ti as the main metal component and further containing another metal element, the mating material can be used rather than the conventional Ti-N based film. It is possible to obtain a sliding member which does not wear out, has good initial familiarity, and has excellent sliding characteristics such as wear resistance and seizure resistance.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 チタン、M群(M;クロム、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/(Ti+M)=1〜
45%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. Titanium, group M (M; chromium, vanadium, zirconium, niobium, molybdenum, hafnium,
Tantalum, one or more metal elements selected from tungsten and aluminum) and nitrogen,
The composition ratio of the metallic elements is M / (Ti + M) = 1 to 1 in atomic% ratio
A sliding member, characterized in that the substrate is coated with a film of 45%.
JP12006193A 1993-05-21 1993-05-21 Sliding member Expired - Fee Related JP3256024B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12006193A JP3256024B2 (en) 1993-05-21 1993-05-21 Sliding member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12006193A JP3256024B2 (en) 1993-05-21 1993-05-21 Sliding member

Publications (2)

Publication Number Publication Date
JPH06330347A true JPH06330347A (en) 1994-11-29
JP3256024B2 JP3256024B2 (en) 2002-02-12

Family

ID=14776926

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12006193A Expired - Fee Related JP3256024B2 (en) 1993-05-21 1993-05-21 Sliding member

Country Status (1)

Country Link
JP (1) JP3256024B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002256968A (en) * 2001-02-26 2002-09-11 Teikoku Piston Ring Co Ltd Sliding member and its manufacturing method
JP2002256967A (en) * 2001-02-26 2002-09-11 Teikoku Piston Ring Co Ltd Sliding member and its manufacturing method
DE102012017731A1 (en) 2012-09-08 2014-03-13 Oerlikon Trading Ag, Trübbach Ti-Al-Ta based coating with improved temperature resistance
WO2018215558A1 (en) 2017-05-23 2018-11-29 Oerlikon Surface Solutions Ag, Pfäffikon Thick TiAlTaN/AlCrN multilayer coating films on turbine components

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002256968A (en) * 2001-02-26 2002-09-11 Teikoku Piston Ring Co Ltd Sliding member and its manufacturing method
JP2002256967A (en) * 2001-02-26 2002-09-11 Teikoku Piston Ring Co Ltd Sliding member and its manufacturing method
JP4656741B2 (en) * 2001-02-26 2011-03-23 帝国ピストンリング株式会社 Sliding member and manufacturing method thereof
JP4666788B2 (en) * 2001-02-26 2011-04-06 帝国ピストンリング株式会社 Sliding member and manufacturing method thereof
DE102012017731A1 (en) 2012-09-08 2014-03-13 Oerlikon Trading Ag, Trübbach Ti-Al-Ta based coating with improved temperature resistance
WO2014037104A1 (en) 2012-09-08 2014-03-13 Oerlikon Trading Ag, Trübbach Ti-al-ta-based coating exhibiting enhanced thermal stability
US9506139B2 (en) 2012-09-08 2016-11-29 Oerlikon Surface Solutions Ag, Pfaffikon Ti—Al—Ta-based coating exhibiting enhanced thermal stability
WO2018215558A1 (en) 2017-05-23 2018-11-29 Oerlikon Surface Solutions Ag, Pfäffikon Thick TiAlTaN/AlCrN multilayer coating films on turbine components

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