JPH03180491A - Sliding member - Google Patents
Sliding memberInfo
- Publication number
- JPH03180491A JPH03180491A JP18804690A JP18804690A JPH03180491A JP H03180491 A JPH03180491 A JP H03180491A JP 18804690 A JP18804690 A JP 18804690A JP 18804690 A JP18804690 A JP 18804690A JP H03180491 A JPH03180491 A JP H03180491A
- Authority
- JP
- Japan
- Prior art keywords
- sliding surface
- sliding member
- fine particles
- composite plating
- particles
- 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
Links
- 238000007747 plating Methods 0.000 claims abstract description 26
- 239000002245 particle Substances 0.000 claims abstract description 24
- 239000002131 composite material Substances 0.000 claims abstract description 13
- 239000007787 solid Substances 0.000 claims abstract description 7
- 229910052796 boron Inorganic materials 0.000 claims abstract description 4
- 239000000314 lubricant Substances 0.000 claims abstract description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910000990 Ni alloy Inorganic materials 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims 1
- 238000005260 corrosion Methods 0.000 abstract description 5
- 230000007797 corrosion Effects 0.000 abstract description 5
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
- 229910052581 Si3N4 Inorganic materials 0.000 abstract description 3
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract description 3
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052982 molybdenum disulfide Inorganic materials 0.000 abstract description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract description 2
- 238000002485 combustion reaction Methods 0.000 abstract description 2
- 229910052961 molybdenite Inorganic materials 0.000 abstract description 2
- 229920003002 synthetic resin Polymers 0.000 abstract description 2
- 239000000057 synthetic resin Substances 0.000 abstract description 2
- 239000010419 fine particle Substances 0.000 abstract 3
- -1 MoS2 Chemical compound 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- WVMHLYQJPRXKLC-UHFFFAOYSA-N borane;n,n-dimethylmethanamine Chemical compound B.CN(C)C WVMHLYQJPRXKLC-UHFFFAOYSA-N 0.000 abstract 1
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- 238000009713 electroplating Methods 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 17
- 239000000203 mixture Substances 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 3
- DDFYFBUWEBINLX-UHFFFAOYSA-M tetramethylammonium bromide Chemical compound [Br-].C[N+](C)(C)C DDFYFBUWEBINLX-UHFFFAOYSA-M 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910001096 P alloy Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 2
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 2
- OFNHPGDEEMZPFG-UHFFFAOYSA-N phosphanylidynenickel Chemical compound [P].[Ni] OFNHPGDEEMZPFG-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 241001629511 Litchi Species 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- 229910007277 Si3 N4 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000012489 doughnuts Nutrition 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000003741 hair volume Effects 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は表面に複合ニッケル合金めっき層が形成された
摺動部材の改良に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an improvement of a sliding member having a composite nickel alloy plating layer formed on its surface.
[従来の技術]
高熱高負荷を受ける内燃機関用ピストンリング等の摺動
部材は耐摩耗性を高めるために硬質クロムめっきが施さ
れることが多いが、クロムめっきは処理に長時間を要す
る上に、めっき廃液の公害防止に多額の費用がかかるた
めにめっきコストが高く、さらに高鉛ガソリンを燃料と
するエンジンに使用すると、耐摩耗性、耐焼付性、耐蝕
性等に問題がある。この問題を解決する方法として、ニ
ッケルーリン合金マトリックス中に、窒化物炭化物、酸
化物等の硬質粒子を分散させる複合めっきが、特公昭5
6−18080号に提案されている。この公知のめっき
は分散粒子の種類、大きさ、分散量を適当に選ぶことに
よって、ある程度の耐摩耗性、耐焼付性、耐蝕性に優れ
た皮膜を形成することが可能であり、すでにシリンダラ
イチ、ピストンリング等の摺動部材に使用されている。[Prior Art] Sliding parts such as piston rings for internal combustion engines that are subjected to high heat and high load are often coated with hard chrome plating to improve wear resistance, but chrome plating requires a long time to process and is difficult to use. Furthermore, plating costs are high because a large amount of money is required to prevent pollution of plating waste liquid, and furthermore, when used in engines that use high-lead gasoline as fuel, there are problems with wear resistance, seizure resistance, corrosion resistance, etc. As a method to solve this problem, composite plating, in which hard particles such as nitrides, carbides, and oxides are dispersed in a nickel-phosphorus alloy matrix, was developed
No. 6-18080. With this known plating, by appropriately selecting the type, size, and amount of dispersed particles, it is possible to form a film with a certain degree of wear resistance, seizure resistance, and corrosion resistance. , used in sliding members such as piston rings.
[発明が解決しようとする課題]
しかし、上記のニー、ケル−リン合金マトリックス中に
硬質粒子を分散させた複合めっき皮膜は高熱高負荷の影
響を受けると皮膜がもろくなりゃすいため、苛酷な条件
で高速運転するエンジンの摺動部材として使用した場合
、耐摩耗性、耐焼付性等は必ずしも満足できるものでは
なかった。[Problems to be Solved by the Invention] However, the above-mentioned composite plating film in which hard particles are dispersed in the Ni-Keirin alloy matrix tends to become brittle when subjected to high heat and high load, so it cannot be used under severe conditions. When used as a sliding member of an engine operating at high speed, wear resistance, seizure resistance, etc. were not necessarily satisfactory.
本発明の目的はこの複合めっきの問題点を解決し、摺動
面に耐摩耗性、#焼付性、耐蝕性に優れた皮膜を形成し
た摺動部材を提供することにある。An object of the present invention is to solve the problems of composite plating and to provide a sliding member having a film formed on the sliding surface with excellent wear resistance, seizure resistance, and corrosion resistance.
[課題を解決するための手段]
前記目的を達成するため、本発明が採用する手段は、金
属製の摺動部材の摺動面に、ポロン0゜1〜lO%を含
有するニッケル合金基地中に、粒径10 pm以下の硬
質粒子及び粒径104m以下の固体y4滑粒子の双方も
しくはいづれか一方を容積比で5〜30%分散共析させ
た複合めっき皮膜を設けたことにある。[Means for Solving the Problems] In order to achieve the above object, the means adopted by the present invention is to apply a nickel alloy matrix containing 0.1 to 10% of poron to the sliding surface of a metal sliding member. A composite plating film is provided in which hard particles with a particle size of 10 pm or less and/or solid Y4 smooth particles with a particle size of 104 m or less are dispersed and co-deposited in a volume ratio of 5 to 30%.
[作用]
ニッケル合金基地中に含まれるポロンは、皮膜硬度を増
し、#摩耗性、耐焼付性、耐蝕性を向上させる効果があ
る。ポロンの量は、0.1〜10毛量%が良い、その理
由は、ポロンの量が0.1%以下ではその効果が少なく
、10%を越すとかえって皮膜が脆くなり、衝撃強度、
密着性も悪くなるからである。[Function] Poron contained in the nickel alloy base has the effect of increasing the hardness of the film and improving wear resistance, seizure resistance, and corrosion resistance. The amount of Poron is preferably 0.1 to 10% by hair volume.The reason is that if the amount of Poron is less than 0.1%, the effect will be small, and if it exceeds 10%, the film will become brittle and the impact strength will decrease.
This is because adhesion also deteriorates.
ニッケル合金基地中に分散させる硬質粒子(例えばS
i3 N4 、S iC,WC,A見203、ZrO2
、Cr203等の1種もしくは2種以上)の粒径及び固
体潤滑粒子(例えば硫化物、ホウ化物、自己潤滑性合成
樹脂の1種もしくは2種以上)の粒径は0.3〜10μ
mがよい、また、分散させる硬質粒子及び固体潤滑粒子
の双方もしくはいずれか一方の量は5〜30容量%が良
い、硬質粒子の粒径が0.3μm以下、あるいは5容量
%以下では耐摩耗性向上の効果は少ない、また、104
m、あるいは30容量%を越えると、皮膜の強度はかえ
って低下し、更に相手材の摩耗を大きくする。Hard particles (e.g. S
i3 N4, S iC, WC, Ami203, ZrO2
, Cr203, etc.) and solid lubricant particles (e.g., sulfide, boride, self-lubricating synthetic resin, one or more types) are 0.3 to 10μ.
In addition, the amount of hard particles and/or solid lubricant particles to be dispersed is preferably 5 to 30% by volume.If the particle size of the hard particles is 0.3 μm or less or 5% by volume or less, wear resistance is reduced. The effect of improving sex is small, and 104
If the amount exceeds m or 30% by volume, the strength of the film will actually decrease and the wear of the mating material will increase.
[実施例] 本発明の摺動部材を実施例について説明する。[Example] Examples of the sliding member of the present invention will be described.
(複合めっき条件及び液組成)
(1)めっき条件
温度 55℃
PH3、5
電流密度 5A/drn’
(2)めっき液組成
比較例−1硫酸ニッケル 240g/交塩化ニッケル
45g/見
ホウ酸 30g/文
窒化珪素(Si3N4.平均粒
径0・7川m)
100 g/文
比較例−2比較例−1のめっき液組成に次亜リン酸3.
0g/見を添加
実施例(本発明品l)比較例−lのめっき液組成にトリ
メチルアミンポラン
(以下TMABと記す)を6゜
0g/l添加
(本発明品2)
硫酸ニッケル 240g/文
塩化ニッケル 45g/文
ホウ酸 30g1交
窒化硼素 100 g/見
(BN、平均粒径2o用m)
TMAB 6 、Og/l(本発明品3)
比較例−1のめっき液組成にT
MABを6・Og/文、二硫化
モリブデン(MoS2、平均粒
径0.1μm)を100 g/fL
添加
上記めっき条件のもとで、比較例−1、比較例−2、実
施M(本発明品1.未発明品2、本発明品3)のそれぞ
れの液組成について複合めっき皮膜を形成した。比較例
−1にTMARを添加するとき、液組成としてホウ酸を
のぞいても硬度は硬くなるが、液の寿命、安定性を考慮
すると、ホウ酸を入れたほうが良い。(Composite plating conditions and liquid composition) (1) Plating condition temperature 55℃ PH3,5 Current density 5A/drn' (2) Comparative example of plating solution composition-1 Nickel sulfate 240g/nickel exchange chloride 45g/boric acid 30g/mon Silicon nitride (Si3N4. Average particle size 0.7 m) 100 g/text Comparative Example-2 Added 3.0% hypophosphorous acid to the plating solution composition of Comparative Example-1.
Example (invention product 1) Addition of 6°0 g/l of trimethylamine poran (hereinafter referred to as TMAB) to the plating solution composition of comparative example-l (invention product 2) Nickel sulfate 240g/invention nickel chloride 45 g/ml boric acid 30 g 1 boron cross-nitride 100 g/ml (BN, average particle size 2 m) TMAB 6, Og/l (inventive product 3) 6.0 g TMAB was added to the plating solution composition of Comparative Example-1. /text, 100 g/fL of molybdenum disulfide (MoS2, average particle size 0.1 μm) was added Under the above plating conditions, Comparative Example-1, Comparative Example-2, Implementation M (Invented product 1. Uninvented product) Composite plating films were formed for each of the liquid compositions of product 2 and product 3). When TMAR is added to Comparative Example-1, the hardness increases even if boric acid is not included in the liquid composition, but when considering the lifespan and stability of the liquid, it is better to add boric acid.
[硬度試験]
前記3種のめっき液で得た複合めっき皮膜について、め
っきしたままのもの及び所定温度で1時間加熱処理後の
もののそれぞれについて、硬度をマイクロビッカース硬
度計で測定した結果を第1図に示す。[Hardness test] The hardness of the composite plating films obtained using the three types of plating solutions was measured using a micro-Vickers hardness meter for the as-plated film and the film after heat treatment at a predetermined temperature for 1 hour. As shown in the figure.
上記結果より、ポロン無添加の場合(比較例−1、−2
)ではめっきしたままの硬度が低く、さらに熱処理温度
300℃で大きな硬度低下を生ずる。それに比べてポロ
ン添加の本発明品(実施例)のものは、めっきしたまま
で、すでに高硬度を示しており、かつ熱処理温度300
〜350℃付近まで高い硬度を雑持するから、ポロンの
添加は、耐熱性の向上にも寄与することがわかる。From the above results, in the case of no addition of poron (Comparative Examples -1, -2)
) has low hardness as plated, and furthermore, a large decrease in hardness occurs at a heat treatment temperature of 300°C. In comparison, the product of the present invention (Example) containing poron already exhibits high hardness as plated, and the heat treatment temperature is 300.
It can be seen that the addition of poron also contributes to improving heat resistance since it maintains high hardness up to around 350°C.
また、比較例−2のようにリン添加皮膜は無添加(比較
例−1)に比べては、硬度向上に効果はある。シ′b)
シ、リン添加皮膜と本発明の実施例(本発明品)のポロ
ン添加皮膜を比べると、ボロン添加皮膜の方が、めっき
したままでも硬度が高く、摺動部材としてより適してい
る。また、リン添加皮膜を苛酷な摺動部材に適用しよう
としたときには、あらかじめ350〜380℃で熱処理
をしてからでないと使用できないが、本発明のポロン添
加皮膜では最初から高硬度であり、熱処理は不要である
か、するとしても300℃以下でよいから、その分コス
トも安くなる。Further, as in Comparative Example-2, the phosphorus-added film is more effective in improving hardness than the non-additive film (Comparative Example-1). C'b)
Comparing the phosphorus-added coating and the poron-added coating of the example of the present invention (product of the present invention), the boron-added coating has higher hardness even as plated, and is more suitable as a sliding member. In addition, when applying a phosphorus-added coating to a harsh sliding member, it cannot be used unless it is heat-treated at 350 to 380°C, but the poron-added coating of the present invention has high hardness from the beginning and cannot be used after heat treatment. is not necessary, or even if it is, the temperature may be lower than 300°C, which reduces the cost accordingly.
[摩耗試験]
比較例−1、比較例−2及び本発明品(実施例)の耐摩
耗性を第1表の摩耗試験条件にて評価した。耐摩耗性試
験は、アムスラー型摩耗試験機を使用し、試験片(18
mmX l 2mmX6mm)を固定片とし、相手材(
回転片)には、ドーナツ状(外径40mm、内径16m
m、厚さ10mm)のものを用いた。形成されためっき
皮膜が、ドーナツ状試験片に接触するようにセットした
。試験結果は第2図に示す。[Abrasion Test] The abrasion resistance of Comparative Example-1, Comparative Example-2, and the product of the present invention (Example) was evaluated under the abrasion test conditions shown in Table 1. For the abrasion resistance test, an Amsler type abrasion tester was used, and test pieces (18
mmX l 2mmX6mm) as the fixed piece, and the mating material (
The rotating piece) has a donut shape (outer diameter 40 mm, inner diameter 16 m).
m, thickness 10 mm) was used. It was set so that the formed plating film was in contact with the doughnut-shaped test piece. The test results are shown in Figure 2.
(スカッフィング性試Vk)
比較例−1,比較例−2及び本発明品(実施例)の耐ス
カッフィング性を第2表のスカッフィング試験条件にて
評価した。この試験結果は、第3図に示す通りである。(Scuffing test Vk) The scuffing resistance of Comparative Example-1, Comparative Example-2, and the product of the present invention (Example) was evaluated under the scuffing test conditions shown in Table 2. The test results are shown in FIG.
第3図から明らかなとお一す、本発明品のN1−B−S
i3N4は、従来の比較例−1(Ni−Si3N4)、
比較例−2(Ni−P−Si3 N4)に比べ耐スカッ
フィング性が向上する。As is clear from Fig. 3, N1-B-S of the product of the present invention
i3N4 is conventional comparative example-1 (Ni-Si3N4),
Scuffing resistance is improved compared to Comparative Example 2 (Ni-P-Si3 N4).
第1表
摩耗試験条件
第2表
スカッフィング試験条件
〔発明の効果〕
上記のとおり、本発明の摺動部材は摺動面に設けられた
複合めっき皮膜が、ニッケルーポロン合金基地に硬質粒
子と固体潤滑粒子の双方もしくはいずれか一方を分散さ
せたものであるから、従来のニッケルーリン合金基地の
ものに比べると、高熱高負荷によってもろくならないと
いう優れた効果を有する。鋳鉄製又はスチール製のピス
トンリング、もしくはシリンダライチ等の表面にニッケ
ルーポロン複合めっきを施して本発明の摺動部材とした
場合、耐摩耗性及び耐スカッフィングが高いので、高温
高負荷のエンジンにも十分に使用することができる。Table 1: Wear test conditions: Table 2: Scuffing test conditions [Effects of the invention] As described above, the sliding member of the present invention has a composite plating film provided on the sliding surface that is formed by combining hard particles and solids on a nickel-poron alloy base. Since it contains both or one of the lubricating particles dispersed therein, it has an excellent effect that it does not become brittle due to high heat and high load compared to conventional nickel-phosphorus alloy base materials. When the sliding member of the present invention is made by applying nickel-poron composite plating to the surface of cast iron or steel piston rings or cylinder litchi, etc., it has high wear resistance and scuffing resistance, so it is suitable for high temperature and high load engines. can also be used adequately.
第1図は熱処理にょ゛る硬度変化を示すグラフ、
第2図は摩耗試験の結果を示すグラフ、第3図はスカッ
フィング試験の結果を示すグラフである。Fig. 1 is a graph showing the change in hardness due to heat treatment, Fig. 2 is a graph showing the results of the wear test, and Fig. 3 is a graph showing the results of the scuffing test.
Claims (1)
中に粒径10μm以下の硬質粒子及び粒径10μm以下
の固体潤滑粒子の双方もしくはいずれか一方を容積比で
5〜30%分散共析する複合めっき皮膜が摺動面に形成
されたことを特徴とする摺動部材。1) Eutectoid dispersion of 5 to 30% by volume of hard particles with a particle size of 10 μm or less and/or solid lubricant particles with a particle size of 10 μm or less in a nickel alloy base containing 0.1 to 10% boron. A sliding member characterized in that a composite plating film is formed on the sliding surface.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18804690A JPH03180491A (en) | 1989-08-11 | 1990-07-18 | Sliding member |
GB919106557A GB9106557D0 (en) | 1990-07-18 | 1991-03-27 | Slidable member |
GB9109588A GB2246145A (en) | 1990-07-18 | 1991-05-02 | Nickel-born alloy composite slidable surface |
DE19914119727 DE4119727A1 (en) | 1990-07-18 | 1991-06-14 | Sliding member, for piston rings |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20666689 | 1989-08-11 | ||
JP1-206666 | 1989-08-11 | ||
JP18804690A JPH03180491A (en) | 1989-08-11 | 1990-07-18 | Sliding member |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03180491A true JPH03180491A (en) | 1991-08-06 |
Family
ID=26504711
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18804690A Pending JPH03180491A (en) | 1989-08-11 | 1990-07-18 | Sliding member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03180491A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100477443B1 (en) * | 2000-12-23 | 2005-03-23 | 재단법인 포항산업과학연구원 | Ni/Ni-B electroplating method for selectively intensified wear-resistance |
KR100675213B1 (en) * | 1999-10-20 | 2007-01-26 | 도와 마이닝 가부시끼가이샤 | Sliding parts with excellent performance in seizure resistance and the making process |
EP2365108B1 (en) * | 2005-12-21 | 2018-05-23 | Bekaert Advanced Cords Aalter NV | A steel wire rope for use in a drive system |
-
1990
- 1990-07-18 JP JP18804690A patent/JPH03180491A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100675213B1 (en) * | 1999-10-20 | 2007-01-26 | 도와 마이닝 가부시끼가이샤 | Sliding parts with excellent performance in seizure resistance and the making process |
KR100477443B1 (en) * | 2000-12-23 | 2005-03-23 | 재단법인 포항산업과학연구원 | Ni/Ni-B electroplating method for selectively intensified wear-resistance |
EP2365108B1 (en) * | 2005-12-21 | 2018-05-23 | Bekaert Advanced Cords Aalter NV | A steel wire rope for use in a drive system |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4790135B2 (en) | Wear-resistant sliding member | |
JP2891745B2 (en) | piston ring | |
JPS61177400A (en) | Wear resistant sliding member | |
JPH03180491A (en) | Sliding member | |
JPS5996295A (en) | Wear resistant sliding parts | |
JPH01210662A (en) | Pneumatic pressure-oil pressure cylinder | |
JP3005263B2 (en) | Sliding member | |
JPS6210236A (en) | Aluminum alloy cylinder | |
JPS58117896A (en) | Sliding member | |
JP2914746B2 (en) | Sliding member | |
JP2865419B2 (en) | piston ring | |
JPS59150080A (en) | Sliding member | |
JPS60196465A (en) | Piston ring | |
GB2246145A (en) | Nickel-born alloy composite slidable surface | |
JPH04175442A (en) | Sliding member | |
JPS6082654A (en) | Sliding member | |
JP3248938B2 (en) | Sliding member | |
JPS589160B2 (en) | Shuyudou Kikou | |
JPS6229749A (en) | Structure of sliding section of internal combustion engine | |
JPS6342143Y2 (en) | ||
JPH03244876A (en) | Combination of piston ring and cylinder | |
JPH0121879B2 (en) | ||
JPH03180490A (en) | Composite plating solution | |
JPS589147B2 (en) | Electroless composite plating method | |
JPH05312269A (en) | Combination of piston ring with cylinder |