JPH0351577A - Oil splashing ring - Google Patents
Oil splashing ringInfo
- Publication number
- JPH0351577A JPH0351577A JP18515389A JP18515389A JPH0351577A JP H0351577 A JPH0351577 A JP H0351577A JP 18515389 A JP18515389 A JP 18515389A JP 18515389 A JP18515389 A JP 18515389A JP H0351577 A JPH0351577 A JP H0351577A
- Authority
- JP
- Japan
- Prior art keywords
- plating layer
- oil
- dispersed
- plating
- plated layer
- 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
- 239000002245 particle Substances 0.000 claims abstract description 41
- 239000000919 ceramic Substances 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims abstract description 6
- 238000007747 plating Methods 0.000 claims description 85
- 239000003921 oil Substances 0.000 abstract description 48
- 239000002131 composite material Substances 0.000 abstract description 16
- 239000006185 dispersion Substances 0.000 abstract description 16
- 229910052581 Si3N4 Inorganic materials 0.000 abstract description 14
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 abstract description 14
- 229910000990 Ni alloy Inorganic materials 0.000 abstract description 13
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract description 13
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 13
- 239000011574 phosphorus Substances 0.000 abstract description 13
- 229910000640 Fe alloy Inorganic materials 0.000 abstract description 11
- 229910052759 nickel Inorganic materials 0.000 abstract description 9
- 230000002093 peripheral effect Effects 0.000 abstract description 5
- 238000005299 abrasion Methods 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract 3
- 239000010410 layer Substances 0.000 description 65
- 230000000052 comparative effect Effects 0.000 description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 14
- 230000000694 effects Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
- 229910017052 cobalt Inorganic materials 0.000 description 7
- 239000010941 cobalt Substances 0.000 description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 7
- 239000011651 chromium Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000010687 lubricating oil Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 5
- 229910052804 chromium Inorganic materials 0.000 description 5
- 230000013011 mating Effects 0.000 description 5
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 238000007790 scraping Methods 0.000 description 4
- 229910003470 tongbaite Inorganic materials 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 3
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 3
- 229910000423 chromium oxide Inorganic materials 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 238000001000 micrograph Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910000677 High-carbon steel Inorganic materials 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229910001105 martensitic stainless steel Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- 238000005121 nitriding Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 229910001030 Iron–nickel alloy Inorganic materials 0.000 description 1
- 229910003217 Ni3Si Inorganic materials 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- 101150065537 SUS4 gene Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000003483 aging Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910000361 cobalt sulfate Inorganic materials 0.000 description 1
- 229940044175 cobalt sulfate Drugs 0.000 description 1
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Pistons, Piston Rings, And Cylinders (AREA)
Abstract
Description
【発明の詳細な説明】
イ.産業上の利用分野
本発明は、油掻きリングに関し、特に、往復動内燃機関
用として好適な油掻きリングに関する。[Detailed description of the invention] a. INDUSTRIAL APPLICATION FIELD The present invention relates to an oil scraper ring, and more particularly to an oil scraper ring suitable for use in a reciprocating internal combustion engine.
口6従来技術
往復動内燃機関では、シリンダ内でピストンが往復動(
多くは上下動)するようになっていて、ピストンリング
がピストンのリング溝に嵌入してその外周面がシリンダ
内周面に対して摺動する。6. Conventional technology In a reciprocating internal combustion engine, a piston reciprocates within a cylinder (
The piston ring fits into the ring groove of the piston, and its outer circumferential surface slides against the inner circumferential surface of the cylinder.
近年、内燃機関の軽量化、高速化、高出力化に伴って油
掻きリングの性能品質、とりわけ油掻き性能を向上して
潤滑柚消費低減に対する要求が高くなってきている。油
掻きリング番よ、その柚掻き性能が向上するよう、シリ
ンダ内周面との摺接面積を小さくして面圧を高めるよう
にしているが、上述のような高度な性能品質要求のため
、油掻きリングは、シリンダ内周面に対して摺動する摺
動部と、この摺動部を背面から押してシリンダ内向面に
高い面圧を以て押付けるためのエキスパンダとからなっ
ている。ところで、上述のような内燃機関の趨勢から、
油掻きリングの摺動部の外周面(シリンダ内面との摺動
面)の摩耗や焼付きが起こり易くなるばかりでなく、背
面もエキスパンダの強い押圧力によって摩耗し、これら
の摩耗によって高い面圧を維持できなくなり、オイル消
費が増大するという問題が生ずるようになってきている
。そこで、摺動部の外周面と背面との双方に硬質クロム
めっきや窒化処理を施した油掻きリングが使用されるよ
うになってきている。然し、硬質クロムめっき層は焼付
きが起こり易く、苛酷な摺動条件になると耐摩耗性が充
分ではない。窒化層は耐摩耗性に優れてはいるが、苛酷
な摺動条件下では耐焼付き性が必ずしも満足し得る程度
ではなく、初期馴染み性が良好ではなく、運転初期のオ
イル消費量が多い。In recent years, as internal combustion engines have become lighter, faster, and have higher output, there has been an increasing demand for improving the performance quality of oil scraping rings, particularly for improving oil scraping performance and reducing consumption of lubricating oil. As for the oil scraping ring, in order to improve its peeling performance, the sliding contact area with the inner peripheral surface of the cylinder is reduced to increase the surface pressure, but due to the high performance and quality requirements mentioned above, The oil scraper ring consists of a sliding part that slides against the inner circumferential surface of the cylinder, and an expander that pushes this sliding part from the back and presses it against the inner surface of the cylinder with high surface pressure. By the way, from the above-mentioned trends in internal combustion engines,
Not only is the outer circumferential surface of the sliding part of the oil scraper ring (the sliding surface with the inner surface of the cylinder) prone to wear and seizure, but the back surface is also worn due to the strong pressing force of the expander, and this wear causes the high surface Problems have arisen in that pressure cannot be maintained and oil consumption increases. Therefore, oil scraping rings in which both the outer circumferential surface and the back surface of the sliding part are hard chromium plated or nitrided are being used. However, the hard chrome plating layer is prone to seizure and does not have sufficient wear resistance under severe sliding conditions. Although the nitrided layer has excellent wear resistance, the seizure resistance is not necessarily satisfactory under severe sliding conditions, the initial conformability is not good, and oil consumption is large at the beginning of operation.
ハ.発明の1」的
本発明は、苛酷な摺動条件下でも、耐摩耗性、耐焼付き
性共に優れかつオイル消費が増大することのない油掻き
リングを提供することを目的としている。C. An object of the present invention is to provide an oil scraper ring that has excellent wear resistance and seizure resistance even under severe sliding conditions and does not increase oil consumption.
二.発明の構威
本発明は、シリンダ内周面に対して摺動する摺動部とこ
の摺動部を背後から押圧する弾性手段とからなる油掻き
リングにおいて、前記摺動部の外周面と前記弾性手段が
当接する前記摺動部の背面とに、金属基地中に硬質セラ
ミックス粒子が分散した組織を有するめっき層が形成さ
れていることを特徴とする油掻きリングに係る。two. Structure of the Invention The present invention provides an oil scraper ring comprising a sliding part that slides against the inner circumferential surface of a cylinder and an elastic means that presses the sliding part from behind. The oil scraper ring is characterized in that a plating layer having a structure in which hard ceramic particles are dispersed in a metal base is formed on the back surface of the sliding portion that the elastic means comes into contact with.
ホ.実施例 以下、本発明の実施例を説明する。Ho. Example Examples of the present invention will be described below.
先ず、本発明に好適なめっき層について説明する。めっ
き層としては、次の2種類のものが特に好適である。そ
の一つは、10〜50重量%コバルト、2〜10重量%
燐を含有するニッケル合金の基地中に、金属の炭化物、
窒化物及び/又は酸化物からなりかつ粒径5μm以下の
硬質セラくツクス粒子が5〜30容積%分散した組織の
めっき層(所謂複合分散めっき層)である。他の一つは
、2〜10重量%燐を含有する鉄合金を基地とし、その
他は上記のめっき層と同様とした複合分散めっき層であ
る。ニッケル又は鉄を主威分とするめっき層は、陰極と
の距離によるめっき層の厚さの変化が比較的少なく(所
謂めっき付き廻り性が良好)、摺動部の窓等の空間を通
って電流が流れることにより、摺動部外周面へのめっき
と同時にその背面にめっき層が形成される。従って、1
回のめっき処理で両面にめっき層が形或できるので、生
産性の観点から頗る好都合である。これに対して、クロ
ムめっきでは、内外周面を同時にはめっきできず、内外
周の両面にめっき層を形戒するにはめっき作業を2回行
わねばならない。First, a plating layer suitable for the present invention will be explained. The following two types of plating layers are particularly suitable. One of them is 10-50% by weight cobalt, 2-10% by weight
In the base of nickel alloy containing phosphorus, metal carbide,
This is a plating layer (so-called composite dispersion plating layer) having a structure in which 5 to 30 volume % of hard ceramic particles made of nitride and/or oxide and having a particle size of 5 μm or less are dispersed. The other one is a composite dispersion plating layer that is based on an iron alloy containing 2 to 10% by weight of phosphorus and is otherwise similar to the above-mentioned plating layer. The plating layer, whose main component is nickel or iron, has relatively little change in thickness depending on the distance from the cathode (so-called good plating coverage), and the plating layer does not change easily through spaces such as windows of sliding parts. As a result of the current flowing, a plating layer is formed on the back surface of the sliding portion at the same time as plating the outer circumferential surface of the sliding portion. Therefore, 1
Since plating layers can be formed on both sides in one plating process, this is very convenient from the viewpoint of productivity. On the other hand, with chrome plating, the inner and outer peripheral surfaces cannot be plated at the same time, and the plating operation must be performed twice to form a plating layer on both the inner and outer peripheral surfaces.
次に、上記のめっき層の組戒について説明する。Next, the rules for assembling the above-mentioned plating layer will be explained.
コバルトはニッケル中に固溶して基地の硬度を上げ、耐
摩耗性、耐焼付き性を改善すると共に表面層の圧壊強度
及び疲労強度を向上させる。基地中のコバルト含有量が
10重量%以−ヒで上記の効果が顕著になる。また上記
コバルト含有量が50重量%を超えると、コスト高にな
ると共に、相対的にニッケル含有量が少なくなって、後
述するNi3Pの生威量が少なく、表面層の機械的強度
が十分には改善されず、その結果、耐摩耗性、耐焼付き
性改善の効果が不十分になる。従って基地中のコバルト
含有量は10〜50重量%以下とするのが良い。Cobalt dissolves in nickel to increase the hardness of the base, improve wear resistance and seizure resistance, and improve the crushing strength and fatigue strength of the surface layer. The above effect becomes remarkable when the cobalt content in the base is 10% by weight or more. Furthermore, if the cobalt content exceeds 50% by weight, the cost will increase and the nickel content will be relatively low, resulting in a small yield of Ni3P, which will be described later, and the mechanical strength of the surface layer will not be sufficient. As a result, the effects of improving wear resistance and seizure resistance become insufficient. Therefore, the cobalt content in the base is preferably 10 to 50% by weight or less.
燐は、熱処理によって基地の硬度を上げて耐摩耗性、耐
焼付き性改善に寄与する。即ち、ニッケル又は鉄と燐と
が反応して基地中にNi3P又はFe3Pの相が」二成
し、時効硬化に於4Jる析出相による機械的強度改善に
類似したメカニズムによって基地の硬度を上げ、これに
よって耐摩耗性改善に寄与する。かくして基地の硬度は
650〜800 1−1.,に」二昇して耐摩耗性、耐
焼付き性が更に改善される。Phosphorus increases the hardness of the base through heat treatment and contributes to improving wear resistance and seizure resistance. That is, nickel or iron reacts with phosphorus to form a Ni3P or Fe3P phase in the base, increasing the hardness of the base by a mechanism similar to the mechanical strength improvement due to the precipitated phase in age hardening. This contributes to improving wear resistance. Thus, the hardness of the base is 650-800 1-1. , the wear resistance and seizure resistance are further improved.
熱処理は400’Cに加熱の熱処理で良い。The heat treatment may be performed by heating to 400'C.
基地中の燐含有量が2重景%未満では上記の効果が顕著
ではなく、これが10重量%を超えると基地が脆くなっ
てめっき層の衝撃強度や母材への被着性が悪くなり、そ
の結果、耐摩耗性、耐焼付き性も劣化する。If the phosphorus content in the base is less than 2% by weight, the above effect will not be noticeable, and if it exceeds 10% by weight, the base will become brittle and the impact strength of the plating layer and adhesion to the base material will deteriorate. As a result, wear resistance and seizure resistance also deteriorate.
硬質セラミックス粒子は基地中に分散してハードスポッ
トを形成し、耐摩耗性、耐焼付き性改着に寄与する。然
し、炭化珪素のような鋭い端面を持たず、相手シリンダ
の内周面を摩耗させる作用は少ない。その粒径が10μ
mを超えて大きくなるとこの粒子がアブレイシブ材とし
て作用し、却って油掻きリング、シリンダの摩耗が進行
するようになる。また粒子の分散量は、5容積%未満で
は耐摩耗性、耐焼付き性改善の効果が顕著ではなく、こ
れが30容積%を超えるとめっき層の機械的強度が低下
して却って耐摩耗性が劣化するようになると共に相手シ
リンダを摩耗させるようになる。従って、基地中に粒径
5μm以下、特に好ましくは0.3〜5μmの硬質セラ
ミックス粒子を5〜30容積%分散させるのが良い。硬
質セラミックス粒子としては、例えば窒化珪素(Si:
+N4)、酸化クロム(Crz(L+)、炭化クロム(
Cr,C2)等の粒子が好適である。めっき層のニッケ
ル合金基地中に窒化珪素粒子を分散させると、400゜
C加熱の熱処理を施すことによって粒子表面にNi,I
Sjが生威して基地と粒子との接着効果が顕れ、めっき
層の機械的強度が一層改善される。加熱温度が高過ぎる
と前記の接着効果が低減する。例えば600“Cに4分
間加熱すると窒化珪素粒子の略全量がNi3Siになっ
てしまう。また窒化珪素の粒子による前記の耐摩耗性、
耐焼付き性改善の効果もなくなってしまう。The hard ceramic particles are dispersed in the matrix to form hard spots, contributing to wear resistance and seizure resistance. However, unlike silicon carbide, it does not have a sharp end surface and has little effect of abrading the inner circumferential surface of the mating cylinder. Its particle size is 10μ
When the particle size exceeds m, the particles act as an abrasive material, and the wear of the oil scraper ring and cylinder is accelerated. Furthermore, if the amount of particles dispersed is less than 5% by volume, the effect of improving wear resistance and seizure resistance will not be significant, and if it exceeds 30% by volume, the mechanical strength of the plating layer will decrease and the wear resistance will deteriorate. At the same time, the mating cylinder begins to wear out. Therefore, it is preferable to disperse 5 to 30% by volume of hard ceramic particles having a particle size of 5 μm or less, particularly preferably 0.3 to 5 μm, in the matrix. Examples of hard ceramic particles include silicon nitride (Si:
+N4), chromium oxide (Crz(L+), chromium carbide (
Particles such as Cr, C2) are suitable. When silicon nitride particles are dispersed in the nickel alloy base of the plating layer, Ni and I are added to the particle surface by heat treatment at 400°C.
Sj grows and exhibits an adhesion effect between the base and particles, further improving the mechanical strength of the plating layer. If the heating temperature is too high, the adhesive effect described above will be reduced. For example, when heated to 600"C for 4 minutes, almost all of the silicon nitride particles become Ni3Si. Also, the wear resistance due to the silicon nitride particles,
The effect of improving seizure resistance is also lost.
摺動部の材料としては、充分な剛性を示す比較的高炭素
の鋼が好適である。前述のめっき層の下地として窒化層
を設ける場合は、窒素との親和力の強いクロムを含有す
るもの、例えばマルテンサイト系ステンレス鋼SUS4
40B等が好適である。As the material for the sliding part, relatively high carbon steel that exhibits sufficient rigidity is suitable. When providing a nitrided layer as the base of the plating layer described above, use a material containing chromium, which has a strong affinity for nitrogen, such as martensitic stainless steel SUS4.
40B etc. are suitable.
エキスパンダの材料としては、ばね性を高ずる比較的高
炭素の鋼が好適である。As the material for the expander, relatively high carbon steel is preferred because it has high spring properties.
次に、焼付き試験及び摩耗試験について説明する。Next, a seizure test and a wear test will be explained.
マルテンサイト系ステンレスll4sUs440B(0
.75 〜0.95%C、≦1.0%Si 、≦1.0
%Mn、≦0.040%P1≦0.030%S1≦0.
60%Ni , 16.0〜18.0%Cr、≦0.7
5%Mo (いずれも重量%))の供試材を用意し、
この{Jt試材から5 mm X 5 mm X10馴
の試験片を採取した。これら試験片のうちの一部には正
方形端面にニッケル合金複合分散めっき層を形成させ、
他の一部には正方形端面に鉄合金複合分散めっき層を形
成させた。めっき層の厚さはいずれも100μmで、め
っき後に400゜Cに1時間加熱の熱処理を施した。Martensitic stainless steel ll4sUs440B (0
.. 75 ~0.95%C, ≦1.0%Si, ≦1.0
%Mn, ≦0.040%P1≦0.030%S1≦0.
60%Ni, 16.0-18.0%Cr, ≦0.7
Prepare a sample material of 5%Mo (both weight%),
A 5 mm x 5 mm x 10 size test piece was taken from this {Jt sample material. Some of these test pieces were coated with a nickel alloy composite dispersion plating layer on the square end faces.
An iron alloy composite dispersion plating layer was formed on the other part of the square end face. The thickness of each plating layer was 100 μm, and after plating, heat treatment was performed at 400° C. for 1 hour.
前者のめっき浴としては、硫酸ニッケル、塩化ニッケル
、硫酸コバルト、次亜燐酸ソーダ及び硼酸からなる水溶
液(めっき液)に窒化珪素粉末を懸濁させためっき浴を
使用し、これらの配合量及び窒化珪素粉末の粒径を変化
させてめっき層の組或及び組織を変化させた。The former plating bath uses a plating bath in which silicon nitride powder is suspended in an aqueous solution (plating solution) consisting of nickel sulfate, nickel chloride, cobalt sulfate, sodium hypophosphite, and boric acid, and the blending amount and nitriding bath are The structure and structure of the plating layer were changed by changing the particle size of the silicon powder.
めっき浴の温度は50〜53゜C、電流密度は8A/d
rrr、めっき時間は2.5時間、めっき浴のpHは浴
組戒に応して2.0〜3.0の間の所定の値とした。The temperature of the plating bath was 50-53°C, and the current density was 8A/d.
rrr, the plating time was 2.5 hours, and the pH of the plating bath was set to a predetermined value between 2.0 and 3.0 according to the bath composition regulations.
めっき条件並びにめっき層の組成及び硬度の一例を挙げ
ると、下記第1表、第2表に示す通りである。Examples of the plating conditions and the composition and hardness of the plating layer are shown in Tables 1 and 2 below.
(以下余白)
第
2
表
後者のめっき浴としては、硫酸第一鉄、塩化第一鉄、次
亜燐酸ソーダ及び硼酸からなるめっき液に窒化珪素粉末
を懸濁さセためつき液を使用し、これらの配合量及び窒
化珪素粉末の粒径を変化させた。めっき浴の温度は55
〜57゜C、電流密度は5A/dd、めっき時間は2.
5時間、めっき浴のpHは2.6〜2.8である。Table 2 The latter plating bath uses a plating solution in which silicon nitride powder is suspended in a plating solution consisting of ferrous sulfate, ferrous chloride, sodium hypophosphite, and boric acid. The blending amount and the particle size of the silicon nitride powder were varied. The temperature of the plating bath is 55
~57°C, current density 5A/dd, plating time 2.
For 5 hours, the pH of the plating bath is 2.6-2.8.
めっき条件並びにめっき層のIa戒及び硬度の一例を挙
げると、下記第3表、第4表に示す通りである。Examples of the plating conditions and the Ia and hardness of the plating layer are shown in Tables 3 and 4 below.
(以下余白)
第
3
表
第
4
表
これら試験片と相対的に摺動させる相手材としては、シ
リンダライナ用鋳鉄FC25を使用し、次のような試験
を行った。(The following are blank spaces) Table 3 Table 4 The following tests were conducted using cast iron FC25 for cylinder liners as a mating material that was slid relative to these test pieces.
災仕主拭駄
試験装置は第6図及び第6図の■−■線に沿う矢視断面
図である第7図に概要を図解的に示すものであって、ス
テータホルダ21に取外し可能に(】1)
取付けられた相手円板試験片22の中央には裏側から注
油孔23を通して潤滑泊が注油される。ステータホルダ
21には図示しない油圧装置によって図に於いて右方へ
向けて所定圧力で押圧力Pが作用するようにしてある。The outline of the disaster cleaning cloth test device is schematically shown in FIG. 6 and FIG. 7, which is a sectional view taken along the line ■-■ in FIG. (1) Lubricating oil is applied to the center of the attached mating disc test piece 22 from the back side through the oiling hole 23. A pressing force P is applied to the stator holder 21 by a hydraulic device (not shown) at a predetermined pressure toward the right in the figure.
円板試験片22に相対向してロータ24があり、図示し
ない駆動装置によって所定速度で回転するようにしてあ
る。Iコタ24の円板試験片22に対ずる端面に取付げ
られた試験片保持具24aには正方形端面を摺動面とし
て角柱試験片25が同心円上に等間隔に4個取外し可能
に、かつ円板試験片22に対して摺動自在に取付けてあ
る。A rotor 24 is provided opposite to the disk test piece 22, and is rotated at a predetermined speed by a drive device (not shown). A test piece holder 24a attached to the end face of the I-kota 24 opposite to the disk test piece 22 has a square end face as a sliding surface, and four prismatic test pieces 25 are removable at equal intervals on a concentric circle. It is slidably attached to the disk test piece 22.
このような装置において、ステータ21に所定の押圧力
Pをかけ、所定の面圧で円板試験片22と角柱試験片2
5のめっきN25aとが接触するようにしておいて、注
油孔23から摺動面に所定給油速度で給油しながらロー
タ24を回転させる。In such an apparatus, a predetermined pressing force P is applied to the stator 21, and a disc test piece 22 and a prismatic test piece 2 are separated by a predetermined surface pressure.
The rotor 24 is rotated while lubricating the sliding surface from the lubricating hole 23 at a predetermined lubricating speed.
一定時間毎にステータ21に作用ずる圧力を段階的に増
加してゆき、ローク24の回転によって角柱試験片25
と円板試験片22との摩擦によって(12)
ステータ21に生ずるトルク(摩擦力によって生ずるト
ルク)Tqをスピンドル26を介してロードセル27に
作用せしめ、その変化を動歪計28で読み取り、記録計
29に記録させる。トルクTqが急激に上昇するときに
焼付きが生じたものとし、その大小を以て耐焼付き性の
良否を判断する。The pressure acting on the stator 21 is increased stepwise at regular intervals, and the rotation of the rake 24 causes the prismatic test piece 25 to be
Torque (torque generated by frictional force) Tq generated on the stator 21 by the friction between the disk test piece 22 (12) is applied to the load cell 27 via the spindle 26, the change is read by the dynamic strain meter 28, and the change is read by the recorder. 29 to record. It is assumed that seizure has occurred when the torque Tq rapidly increases, and the quality of the seizure resistance is determined based on the magnitude.
試験条件は次に示す通りである。The test conditions are as follows.
摩擦速度:8m/sec
潤滑油:モータオイル#30を400mR/min給油
接触圧力;試験開始時40kg/c献その後3分間経過
毎に10kg/c+flずつ上昇度且跋駄
第6図、第7図の試験装置を使用し、次のような試験条
件で摩耗試験を行った。Friction speed: 8 m/sec Lubricating oil: Motor oil #30 at 400 mR/min. Contact pressure: 40 kg/c at the start of the test, then increased by 10 kg/c + fl every 3 minutes. Figures 6 and 7 A wear test was conducted using a test device under the following test conditions.
摩擦速度は5m/sec、接触圧力は100kg/al
tに一定、潤滑油はモータオイル#30にダスト(JI
S2種)を0.2g/I!.添加したもの、その他の試
験条件は前記焼付き試験に於けると同じである。Friction speed is 5m/sec, contact pressure is 100kg/al
The lubricating oil is motor oil #30 and dust (JI
S2 types) 0.2g/I! .. The additives and other test conditions were the same as in the seizure test described above.
摩耗量は次のようにして測定した。角柱試験片について
は、試験後に試験片を取り外し、摩耗に(13)
よる高さ寸法の減少を測定した。円板試験片については
、摩耗によって生した円環状の摩耗痕の深さを測定した
。The amount of wear was measured as follows. For the prismatic test piece, the test piece was removed after the test and the reduction in height due to wear (13) was measured. For the disk test piece, the depth of an annular wear scar caused by wear was measured.
試験結果は、第8図〜第14図に示す通りであった。第
8図〜第14図から、ニッゲル合金めっき層の基地は、
2〜10重量%燐、lO〜50重景%コバルトのニッケ
ル合金とし、これらの基地中に分散させる窒化珪素粒子
は、平均粒径を5μm以下、特に0.3〜5μm、分散
量を5〜30容積%とするのが、また、鉄合金めっき層
の基地は2〜10垂量%燐とするのが良い鈷果が得られ
ることが理解できる。これらの図において、摩耗試験の
試験時nilば50分間である。The test results were as shown in FIGS. 8 to 14. From Figures 8 to 14, the base of the Niggel alloy plating layer is
A nickel alloy containing 2 to 10% phosphorus and 1O to 50% cobalt is used, and the silicon nitride particles dispersed in these bases have an average particle diameter of 5 μm or less, particularly 0.3 to 5 μm, and a dispersion amount of 5 to 5 μm. It can be understood that a good effect can be obtained by setting the phosphorus content to 30% by volume, and by setting the base of the iron alloy plating layer to 2 to 10% by volume. In these figures, the test time of the wear test is 50 minutes.
比較のために、同し母材上に、厚さ100μmの硬質ク
ロムめっき層を形成した角柱試験片(比較例1)厚さ1
00μmの窒化層を形成した角柱試験片(比較例2)に
ついて同様の試験を行った。これら比較例の角柱試験片
を、前述の角柱試験片のうち、めっき層の基地を20重
量%コバルト、5重量%燐、残部ニッケルとし、この基
地中に0.3〜(14)
3μmのSiJ4粒子を10容積%分散させたもの(実
施例1)及びめっき層の基地を2重量%燐、残部鉄とし
てこの基地中と実施例1と同様のSiJ4粒子を分散さ
せたもの(実施例2)の試験結果と対比して第15図及
び第16図に示す。なお、第15図中、焼付き発生面圧
が10kg/cilTの間隔の目盛の中間に位置してい
るのは、接触面圧上昇途中に焼付きが発生したことを示
しており、ハッチングを付した領域は、2回の同じ試験
で得られた低い値と高い値との範囲を示している。For comparison, a prismatic test piece (Comparative Example 1) with a hard chromium plating layer of 100 μm thick formed on the same base material was prepared.
A similar test was conducted on a prismatic test piece (Comparative Example 2) on which a nitrided layer of 00 μm was formed. The prismatic test pieces of these comparative examples were the same as the above-mentioned prismatic test pieces, with the base of the plating layer being 20% by weight cobalt, 5% by weight phosphorus, and the balance being nickel, and 0.3 to (14) 3 μm of SiJ4 was added to the base. One in which particles were dispersed at 10% by volume (Example 1), and one in which SiJ4 particles similar to those in Example 1 were dispersed in this base, with the base of the plating layer being 2% by weight phosphorus and the balance iron (Example 2). Figures 15 and 16 show a comparison with the test results. In addition, in Fig. 15, the fact that the surface pressure at which seizure occurs is located in the middle of the scale with intervals of 10 kg/cilT indicates that seizure has occurred while the contact surface pressure is rising, and is marked with hatching. The area shown represents the range of low and high values obtained in two identical tests.
比較例1は、焼付き発生面圧が最も低く、摩耗量も最も
大きい。比較例2は、摩耗量が最も小さく、耐焼付き性
が比較例1に較べて改善されている。これらに対し、実
施例1、2共に摩耗量は比較例2のそれに近く、耐焼付
き性は比較例2に対して更に改善されている。Comparative Example 1 has the lowest seizure-generating surface pressure and the highest amount of wear. Comparative Example 2 has the smallest amount of wear and has improved seizure resistance compared to Comparative Example 1. On the other hand, in both Examples 1 and 2, the wear amount is close to that of Comparative Example 2, and the seizure resistance is further improved compared to Comparative Example 2.
実豊跋験
次に、本発明に基く油掻きリングをエンジンに組付けて
運転した実機試験(ヘンチテスト)について説明する。Next, an actual machine test (Hench test) in which the oil scraper ring according to the present invention was assembled into an engine and operated was explained.
(15)
油掻きリングとしては、第3図に拡大部分斜視図で、第
1図に拡大断面図で示す構造のものを使用した。この油
掻きリングは、本出願人が先に提示(実開昭51112
642号)した形状のものである。(15) As the oil scraper ring, one having a structure shown in an enlarged partial perspective view in FIG. 3 and an enlarged sectional view in FIG. 1 was used. This oil scraper ring was first proposed by the applicant (Utility Model Application No. 51112
No. 642).
油掻きリング1は、硬鋼線材SWRH77Bを圧延して
断面M字形に或形してなる摺動部材2とステンレスli
ilsUs304を加工硬化させたコイルエキスパンダ
6とからなっている。摺動部材2の平行部分2a、2a
の端面にはニッケル合金複合分散めっき層又は鉄合金複
合分散めっき層5A、5Aが形成され、これらめっき層
5A、5Aがシリンダライナ(第4図の16)に対して
摺動する。摺動部材2の谷を形或する部分(断面V字形
の部分)2bの背面には上記と同しめっき層5Dが形成
され、谷の部分2bの底部にはオイルを通ずためのオイ
ル窓4が周方向に等間隔に設けられている。The oil scraper ring 1 consists of a sliding member 2 formed by rolling a hard steel wire SWRH77B into an M-shaped cross section, and a stainless steel wire.
It consists of a coil expander 6 made of work-hardened ilsUs304. Parallel parts 2a, 2a of sliding member 2
A nickel alloy composite dispersion plating layer or an iron alloy composite dispersion plating layer 5A, 5A is formed on the end face of the cylinder, and these plating layers 5A, 5A slide against the cylinder liner (16 in FIG. 4). The same plating layer 5D as above is formed on the back surface of the valley-forming portion 2b (V-shaped cross section) of the sliding member 2, and an oil window for oil to pass through is formed at the bottom of the valley portion 2b. 4 are provided at equal intervals in the circumferential direction.
上記めっき層は、断面M字形の母材3を上下方向に多数
重ね、これを陰極としてめっき浴中で回転させながらめ
っき浴槽の側壁近くの陽極との間でめっき浴を電気分解
して母材3上に被着させて(IG)
形成される。従って、隣同士の摺動部材が接触する平行
部分2aの外面にはめっき層は形成されない。前述した
ように上記のめっき層はめっき付き廻り性が良好なので
、電流が窓4を通って摺動部材内側に流れ、谷の部分2
bの背面にもめっき層5Dが均一な厚さに形成される。The above-mentioned plating layer is formed by stacking a large number of M-shaped base materials 3 in the vertical direction and electrolyzing the plating bath between them and the anode near the side wall of the plating bath while rotating in a plating bath using this as a cathode. 3 (IG) is formed. Therefore, no plating layer is formed on the outer surface of the parallel portion 2a where adjacent sliding members contact each other. As mentioned above, since the above-mentioned plating layer has good plating adhesion properties, the current flows inside the sliding member through the window 4, and the valley part 2
A plating layer 5D is also formed on the back surface of b to have a uniform thickness.
めっき層5Dの厚さはめっき層5Aの厚さの175〜1
/lOとなる。The thickness of the plating layer 5D is 175 to 1 of the thickness of the plating layer 5A.
/lO.
また、平行部分2aの内面から谷の部分2bの外面にも
めっき層5Bが形成され、窓4の面にもめっき層5Cが
形成される。上記めっき層は次のような組成のものであ
る。ニッケル合金複合分散めっき層は、20重量%ニッ
ケル、5重量%燐を含有するニッケル合金基地中に粒径
3μmの窒化珪素粒子が10容積%分散させた構造を有
する。鉄合金複合分散めっき層は、2重量%燐を含有す
る鉄合金基地中に粒径3μmの窒化珪素粒子が5容積%
分散させた構造を有する。Further, a plating layer 5B is also formed on the inner surface of the parallel portion 2a and the outer surface of the valley portion 2b, and a plating layer 5C is also formed on the surface of the window 4. The above plating layer has the following composition. The nickel alloy composite dispersed plating layer has a structure in which 10% by volume of silicon nitride particles having a particle size of 3 μm are dispersed in a nickel alloy base containing 20% by weight of nickel and 5% by weight of phosphorus. The iron alloy composite dispersion plating layer consists of 5% by volume of silicon nitride particles with a particle size of 3 μm in an iron alloy matrix containing 2% by weight of phosphorus.
It has a dispersed structure.
この例では、めっき層5Aの厚さはいずれも100μm
、めっき層5Dの厚さは、ニッケル合金複合分散めっき
層ではl5μm、鉄合金複合分散め(17)
っき層では10μmである。摺動部材2には、めっき後
に400゜Cに1時間加熱の熱処理を施した。第2A図
はニッケル合金複合分散めっき層の組織を示す倍率40
0倍の顕微鏡写真、第2B図は鉄合金複合分散めっき層
の組織を示す倍率400倍の顕微鏡写真である。ニッケ
ル合金又は鉄合金の基地中に灰色を呈する窒化珪素粒子
が均一に分散しているのが観察される。なお、熱処理に
よって析出するNi3P相、NisSi相、Fe.P相
は、極めて微細であるので写真では観察されないが、こ
れらの相の存在はX線回折試験によって確認さクている
。In this example, the thickness of the plating layer 5A is 100 μm.
The thickness of the plating layer 5D is 15 μm for the nickel alloy composite dispersion plating layer, and 10 μm for the iron alloy composite dispersion plating layer (17). After plating, the sliding member 2 was heat-treated at 400°C for 1 hour. Figure 2A shows the structure of the nickel alloy composite dispersion plating layer at a magnification of 40
The micrograph at 0x magnification and Figure 2B are micrographs at 400x magnification showing the structure of the iron alloy composite dispersed plating layer. Gray silicon nitride particles are observed to be uniformly dispersed in the nickel alloy or iron alloy matrix. Note that Ni3P phase, NisSi phase, Fe. The P phase is so fine that it cannot be observed in photographs, but the presence of these phases has been confirmed by X-ray diffraction tests.
コイルエキスパンダ6の母月7の表面には、厚さ10μ
mの硬質クロムめっき層8を形成させた。The surface of the base 7 of the coil expander 6 has a thickness of 10μ.
A hard chromium plating layer 8 of m was formed.
油掻きリング1の呼び径は86mm,幅Bは4mm,厚
さTは2.5mmである。The oil scraper ring 1 has a nominal diameter of 86 mm, a width B of 4 mm, and a thickness T of 2.5 mm.
上記の油掻きリングをボア径86mm、4サイクル、水
冷、4気筒、排気量2000ccのディーゼルエンジン
に組付け、回転数4750rpm 、全負荷で200時
間のペンヂデストを行い、オイル泪費量をη]り定した
。The above oil scraper ring was installed in a 4-stroke, water-cooled, 4-cylinder, 2000 cc diesel engine with a bore diameter of 86 mm, and was subjected to pen de-destination for 200 hours at full load at a rotation speed of 4750 rpm, and the amount of oil depleted was determined by Established.
第4図はエンジンのビス1〜ンリング及びその周辺(I
8)
の拡大断面図である。鋳鉄製のシリンダライナ16にピ
ス1ヘン13が嵌入し、ピストン13のリング溝14A
、14B、14Cには上から順にバレルフェース形の第
一圧カリング11、テーパフェース形の第二圧カリング
12、前記の油掻きリング1が装着されている。油掻き
リング1は、摺動部材2が背面からコイルエキスパンダ
6によって押され、シリンダライナ16の内周面に高面
圧で押付けられる。図中、17は水冷ジャケットである
。Figure 4 shows the engine screws 1 to 1 ring and their surroundings (I
8) is an enlarged sectional view of. The piston 1 hem 13 is fitted into the cast iron cylinder liner 16, and the ring groove 14A of the piston 13 is inserted into the cylinder liner 16 made of cast iron.
, 14B, and 14C are equipped with a barrel face-shaped first pressure culling 11, a tapered face-shaped second pressure culling 12, and the above-mentioned oil scraper ring 1 in order from the top. In the oil scraper ring 1, the sliding member 2 is pushed from the back side by the coil expander 6, and is pressed against the inner circumferential surface of the cylinder liner 16 with high surface pressure. In the figure, 17 is a water cooling jacket.
測定結果は第5図に示す通りである。同図では、比較の
ために、第1図のめっき層5A及び5Dの箇所に厚さ1
00μmの硬質クロムめっき層を形成させた油掻きリン
グ(比較例1)及び同箇所にガス窒化によって窒化層を
形成させた油掻きリング(比較例2)について同様の試
験を行った結果が併記してある。The measurement results are shown in FIG. In the figure, for comparison, the plating layers 5A and 5D in Figure 1 have a thickness of 1
The results of similar tests on an oil scraper ring with a 00μm hard chrome plating layer (Comparative Example 1) and an oil scraper ring with a nitrided layer formed at the same location by gas nitriding (Comparative Example 2) are also listed. There is.
オイル消費量は、実施例l、実施例2、比較例1の順と
良好であり、これらは50時間の運転で変化が略なくな
る。比較例2では窒化層の初期馴染み性が良好ではない
ため、100時間の運転迄オイ(19)
ル消費が漸減していて、オイル消費量が大きい。The oil consumption was good in the order of Example 1, Example 2, and Comparative Example 1, and there was almost no change in these after 50 hours of operation. In Comparative Example 2, the initial conformability of the nitrided layer was not good, so oil consumption gradually decreased until 100 hours of operation, resulting in a large amount of oil consumption.
なお、実施例1、2の窒化珪素粒子に替えて、酸化クロ
ム(crzoz)粒子を分散させた例(実施例3、4)
、同しく炭化クロム(Cr3C4)粒子を分散させた例
(実施例5、6)について同様の試験を行ったところ、
100時間運転の時点でオイル消費量は下記第5表に示
す通りであって、良好な結果を示した。酸化クロム粒子
、炭化クロム粒子の粒径及び分散量は、実施例■、2と
同しにしてある。In addition, examples in which chromium oxide (crzoz) particles were dispersed instead of the silicon nitride particles in Examples 1 and 2 (Examples 3 and 4)
Similar tests were conducted on examples (Examples 5 and 6) in which chromium carbide (Cr3C4) particles were also dispersed.
The oil consumption after 100 hours of operation was as shown in Table 5 below, indicating good results. The particle diameters and dispersion amounts of the chromium oxide particles and chromium carbide particles are the same as in Examples 1 and 2.
200時間運転後、コイルエキスパンダの喰い込みによ
って摺動部材背面に生じた凹部の深さは、実施例1〜6
ではいずれも2μmであった。これに対して比較例1で
は40μmの深さであった。なお、摺動部材背面にマス
キングして表面を母柑の債とした油掻きリングにあって
は、上記凹部の深さは110μmであった。この結果か
ら、第5図では比較例lはオイル消費量が実施例のそれ
と大差ないとしても、更に長時間の運転になるとオイル
消費が増大するものと判断される。After 200 hours of operation, the depth of the recess formed on the back surface of the sliding member due to the biting of the coil expander was as in Examples 1 to 6.
In both cases, the thickness was 2 μm. On the other hand, in Comparative Example 1, the depth was 40 μm. In addition, in the case of the oil scraper ring in which the back surface of the sliding member was masked and the surface was covered with mother-of-pearl, the depth of the recess was 110 μm. From this result, in FIG. 5, it is determined that although the oil consumption of Comparative Example 1 is not much different from that of the Example, the oil consumption increases with longer operation.
以上の焼付き試験、摩耗試験及び実機試験の結果から、
本発明に基く油掻きリングは、優れた耐焼付き性、耐摩
耗性を示して耐久性に優れており、初期馴染み性が良好
で運転初期から長時間に亘って良好なオイル供給機能を
発揮し、かつオイル消費が少なく、経済的であることが
解る。From the results of the above seizure test, wear test, and actual machine test,
The oil scraper ring based on the present invention exhibits excellent seizure resistance and abrasion resistance, and has excellent durability.It also has good initial adaptability and exhibits a good oil supply function for a long period of time from the beginning of operation. , and low oil consumption, making it economical.
なお、油掻きリングの形状は、上記の例に限られるもの
ではなく、上下2枚のレール(摺動部材)とこれを背後
から押すプレートエキスパンダ又はスベーサエキスパン
ダとを備えたプレートエキスパンダ付き油掻きリング又
はスベーサエキスパンダ付き油掻きリングに本発明を適
用して同様の効果が奏せられる。Note that the shape of the oil scraper ring is not limited to the above example; it may also be a plate expander that has two rails (sliding members), upper and lower, and a plate expander or sub-expander that pushes the rails from behind. Similar effects can be obtained by applying the present invention to an oil scraper ring with an expander or an oil scraper ring with a smooth expander.
へ.発明の効果
本発明は、摺動部の外周面と弾性手段が当接す(2l)
(zUノ
る背面とに、金属基地中に硬質セラミックス粒子が分散
した組織を有するめっき層が形成されているので、この
めっき層の−1二記組織に起因する優れた耐焼付き性及
び耐摩北性によって苛酷な使用条件下にあっても優れた
耐久性を示し、かつ、上記めっき層の優れた耐焼付き性
、耐摩耗性に加えて良好な初期馴染み性によって機関の
運転初1リ1から長期間に亘って良好な潤滑油供給機能
を果たすと共に潤滑油消費量も少なくて済む。fart. Effects of the Invention The present invention is characterized in that a plating layer having a structure in which hard ceramic particles are dispersed in a metal base is formed on the outer peripheral surface of the sliding part and the back surface of the elastic means (2l) (zU). Therefore, it shows excellent durability even under severe usage conditions due to the excellent seizure resistance and wear resistance due to the -12 structure of this plating layer, and In addition to good adhesion and abrasion resistance, it also has good initial run-in, so it performs a good lubricating oil supply function over a long period of time from the first engine operation, and consumes less lubricating oil.
図面はいずれも本発明の実施例を示すものであって、
第1図は油掻きリングの拡大断面図、
第2A図及び第2B図は夫々めっき層の金属組織を示す
顕微鏡写真、
第3図は油掻きリングの拡大部分斜視図、第4図は油掻
きリング及び圧力リングを組付けたヂイーゼルエンジン
の拡大部分断面図、第5図は実機試験の結果を示すグラ
フ、第6図は焼付き試験、摩耗試験の装置の要部を(2
2)
示す一部破砕概略図、
第7図は第6図の■−■線矢視断面図、第8図、第9図
、第10図、第11図、第12図、第13図及び第14
図はめっ゛き層の組威と耐焼付き性又は耐摩耗性との関
係港示すグラフ、第15図は焼付き試験の結果を比較例
と対比して示すグラフ、
第16図は摩耗試験の結果を比較例と対比して示すグラ
フ
である。
なお、図面に示された符号において、
1・・・・・・・・・油掻きリング
2・・・・・・・・・摺動部材
3・・・・・・・・・摺動部材の母材
4・・・・・・・・・オイル窓
5A、5B、5C、5D,25a
・・・・・・・・・めっき層
6・・・・・・・・・コイルエキスパンダ7・・・・・
・・・・コイルエキスパンダの母材8・・・・・・・・
・硬質クロムめっき層(23)
11、12・・・・・・・・・圧力リング13・・・・
・・・・・ピストン
16・・・・・・・・・シリンダライナ21・・・・・
・・・・ステータ
22・・・・・・・・・円板試験片(相手摺動試験片)
23・・・・・・・・・注油孔
24・・・・・・・・・ロータ
25・・・・・・・・・角柱試験片
である。The drawings all show examples of the present invention, and FIG. 1 is an enlarged sectional view of an oil scraper ring, FIGS. 2A and 2B are micrographs showing the metal structure of the plating layer, and FIG. 3 Figure 4 is an enlarged partial cross-sectional view of the diesel engine with the oil scraper ring and pressure ring assembled, Figure 5 is a graph showing the results of actual machine tests, and Figure 6 is a graph showing the results of the actual engine test. The main parts of the equipment for wear tests and abrasion tests (2
2) A partially fractured schematic diagram shown in Figure 7 is a sectional view taken along the line ■-■ in Figure 6, Figures 8, 9, 10, 11, 12, 13, and 14th
Figure 15 is a graph showing the relationship between the strength of the plated layer and seizure resistance or wear resistance. Figure 15 is a graph showing the results of the seizure test in comparison with a comparative example. It is a graph showing the results in comparison with a comparative example. In addition, in the symbols shown in the drawings, 1... Oil scraper ring 2... Sliding member 3... Sliding member. Base material 4...Oil windows 5A, 5B, 5C, 5D, 25a...Plating layer 6...Coil expander 7... ...
...Coil expander base material 8...
・Hard chrome plating layer (23) 11, 12... Pressure ring 13...
... Piston 16 ... Cylinder liner 21 ...
...Stator 22...Disc test piece (mating sliding test piece)
23... Oil filling hole 24... Rotor 25... It is a prismatic test piece.
Claims (1)
部を背後から押圧する弾性手段とからなる油掻きリング
において、前記摺動部の外周面と前記弾性手段が当接す
る前記摺動部の背面とに、金属基地中に硬質セラミック
ス粒子が分散した組織を有するめっき層が形成されてい
ることを特徴とする油掻きリング。1. In an oil scraper ring consisting of a sliding part that slides against the inner circumferential surface of the cylinder and an elastic means that presses the sliding part from behind, the outer circumferential surface of the sliding part and the elastic means contact with each other. An oil scraper ring characterized in that a plating layer having a structure in which hard ceramic particles are dispersed in a metal base is formed on the back surface of the sliding part.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18515389A JPH0351577A (en) | 1989-07-17 | 1989-07-17 | Oil splashing ring |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18515389A JPH0351577A (en) | 1989-07-17 | 1989-07-17 | Oil splashing ring |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0351577A true JPH0351577A (en) | 1991-03-05 |
Family
ID=16165780
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18515389A Pending JPH0351577A (en) | 1989-07-17 | 1989-07-17 | Oil splashing ring |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0351577A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001138663A (en) * | 1999-09-17 | 2001-05-22 | Grapha Holding Ag | Joining device for applying adhesive to back or contact region of passing book block |
-
1989
- 1989-07-17 JP JP18515389A patent/JPH0351577A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001138663A (en) * | 1999-09-17 | 2001-05-22 | Grapha Holding Ag | Joining device for applying adhesive to back or contact region of passing book block |
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