JPS61231154A - Wear resisting surface layer - Google Patents
Wear resisting surface layerInfo
- Publication number
- JPS61231154A JPS61231154A JP60072343A JP7234385A JPS61231154A JP S61231154 A JPS61231154 A JP S61231154A JP 60072343 A JP60072343 A JP 60072343A JP 7234385 A JP7234385 A JP 7234385A JP S61231154 A JPS61231154 A JP S61231154A
- Authority
- JP
- Japan
- Prior art keywords
- surface layer
- wear
- test
- nickel
- sprayed
- 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
Links
- 239000002344 surface layer Substances 0.000 title claims abstract description 42
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 24
- 239000000956 alloy Substances 0.000 claims abstract description 24
- 239000011230 binding agent Substances 0.000 claims abstract description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 27
- 239000000843 powder Substances 0.000 claims description 20
- 239000002245 particle Substances 0.000 claims description 16
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 14
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 14
- 229910052759 nickel Inorganic materials 0.000 claims description 13
- 239000000463 material Substances 0.000 description 13
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 230000013011 mating Effects 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 229910052796 boron Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052750 molybdenum Inorganic materials 0.000 description 4
- 239000011733 molybdenum Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000007750 plasma spraying Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 229910000623 nickel–chromium alloy Inorganic materials 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000007751 thermal spraying Methods 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000604 Ferrochrome Inorganic materials 0.000 description 1
- 229910005091 Si3N Inorganic materials 0.000 description 1
- LNSPFAOULBTYBI-UHFFFAOYSA-N [O].C#C Chemical group [O].C#C LNSPFAOULBTYBI-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- GVEHJMMRQRRJPM-UHFFFAOYSA-N chromium(2+);methanidylidynechromium Chemical compound [Cr+2].[Cr]#[C-].[Cr]#[C-] GVEHJMMRQRRJPM-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 229910052574 oxide ceramic Inorganic materials 0.000 description 1
- 239000011224 oxide ceramic Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 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
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910003470 tongbaite Inorganic materials 0.000 description 1
Landscapes
- Cylinder Crankcases Of Internal Combustion Engines (AREA)
- Coating By Spraying Or Casting (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
Description
【発明の詳細な説明】 イ、産業上の利用分野 本発明は耐摩耗性表面層に関する。[Detailed description of the invention] B. Industrial application field The present invention relates to wear-resistant surface layers.
口、従来技術
近年、内燃機関はその性能向上のために高圧縮比化、高
速回転化が図られ、これに伴ってピストンリング等の摺
動部品には従来以上に優れた耐摩耗性、耐焼付性(耐ス
カツフ性)が要求されるようになってきている。In recent years, internal combustion engines have been designed to have higher compression ratios and faster rotation speeds in order to improve their performance, and as a result, sliding parts such as piston rings have become more resistant to wear and tear than ever before. Seizure resistance (scuff resistance) is increasingly required.
ロムめっき層は、硬度が高(、それ自体の摩耗、摺動相
手材の摩耗共に少な(、極めて優れた耐摩耗性を示すも
のであるが、保油性に乏しく、高温、高負荷の条件下で
は、摺動中に焼付を起こし易いという欠点を有している
。The ROM plating layer has high hardness (low wear on itself and low wear on the material it slides on), and exhibits extremely excellent wear resistance, but it has poor oil retention and is difficult to handle under high temperature and high load conditions. However, this has the disadvantage that seizure is likely to occur during sliding.
耐焼付性の改善された表面層としては、モリブデン溶射
表面層が一部に採用されている。モリブデン溶射表面層
は、気孔を内在しているので保油性が良好であり、而も
融点が高いことがら、耐焼付性に優れているのであるが
、その耐摩耗性は硬質クロムめっき層のそれに較べて可
なり劣っており、その上、高温で酸化されやすく、寿命
が短いという欠点を有している。As a surface layer with improved seizure resistance, a molybdenum sprayed surface layer is used in some cases. The molybdenum sprayed surface layer has good oil retention properties because it contains pores, and has excellent seizure resistance because of its high melting point, but its wear resistance is comparable to that of a hard chrome plating layer. In addition, it has the disadvantage of being easily oxidized at high temperatures and having a short lifespan.
モリブデン溶射表面層の上記欠点を解消する溶射表面層
として、フェロクロム粉、モリブデン扮及ヒニッケルー
クロム合金粉からなる混合粉をプラズマ溶射してなる溶
射表面層が一部で採用されている。然し、この溶射表面
層もモリブデンを含有するために高温で酸化されやす(
、寿命の点で問題である。As a thermal sprayed surface layer that eliminates the above-mentioned drawbacks of the molybdenum thermal sprayed surface layer, a thermal sprayed surface layer formed by plasma spraying a mixed powder of ferrochrome powder, molybdenum powder, and nickel-chromium alloy powder has been adopted in some cases. However, since this sprayed surface layer also contains molybdenum, it is easily oxidized at high temperatures (
, which is a problem in terms of service life.
また、チタニア(TiOz)、アルミナーチタニア(A
7!zo3−13重量%Tio2又はAfzO3−40
重量%T iO2) 、酸化クロム(Cr203)、ジ
ルコニア−イツトリア(Zr02 8〜12重量%Y2
O3)などの酸化物系セラミックスをプラズマ溶射して
なる溶射表面層も試みられているが、耐熱衝撃性に劣る
ことと脆いという欠点を有している。In addition, titania (TiOz), alumina titania (A
7! zo3-13 wt% Tio2 or AfzO3-40
wt% TiO2), chromium oxide (Cr203), zirconia-ittria (Zr02) 8-12 wt% Y2
A thermal sprayed surface layer formed by plasma spraying an oxide ceramic such as O3) has also been attempted, but it has the drawbacks of poor thermal shock resistance and brittleness.
セラミックス溶射表面層の耐熱衝撃性と脆性の問題を解
決するため、チタニア粉、アルミナ粉又は両者の混合粉
とニッケルークロム合金粉又はニッケルーアルミニウム
合金粉とからなる混合粉を爆射してなる溶射表面層が考
えられるが、セラミック粒子と合金粒子との粘度差や比
重差のために、均一な溶射表面層を得ることが困難であ
る。In order to solve the problem of thermal shock resistance and brittleness of the thermal sprayed ceramic surface layer, a mixed powder consisting of titania powder, alumina powder, or a mixture of both, and nickel-chromium alloy powder or nickel-aluminum alloy powder is sprayed. A thermally sprayed surface layer is considered, but it is difficult to obtain a uniform thermally sprayed surface layer due to the difference in viscosity and specific gravity between the ceramic particles and the alloy particles.
上記のような次第で、高温、高負荷の摺動条件下で充分
に満足し得る摺動特性を示す表面層は未だ得られていな
い。As described above, a surface layer that exhibits fully satisfactory sliding characteristics under high temperature and high load sliding conditions has not yet been obtained.
ハ、発明の目的
本発明は、上記の事情に鑑みてなされたものであって、
高温、高負荷の摺動条件下でも優れた耐摩耗性、耐焼付
性を示す表面層飲を提供することを目的としている。C. Purpose of the Invention The present invention has been made in view of the above circumstances, and includes:
The objective is to provide a surface layer that exhibits excellent wear resistance and seizure resistance even under high temperature and high load sliding conditions.
二、発明の構成
即ち、本発明は、結合材としてのニッケル基自溶合金が
10〜50重量%、残部が粒径1〜74μmの酸化クロ
ム粉末から実質的になる耐摩耗性表面層に係る。2. Structure of the invention, that is, the present invention relates to a wear-resistant surface layer consisting essentially of 10 to 50% by weight of a nickel-based self-fluxing alloy as a binder, and the remainder consisting of chromium oxide powder with a particle size of 1 to 74 μm. .
自溶合金は、ニッケル基自溶合金とコバルト基自溶合金
とに大別される。ニッケル基自溶合金は、Hv550〜
800と硬度が高く、酸化クロム(CrzO3)の硬度
HV2O3−1200に近いので、酸化クロム粉末の結
合材として耐摩耗性表面層を形成するのに好適である。Self-fluxing alloys are broadly classified into nickel-based self-fluxing alloys and cobalt-based self-fluxing alloys. Nickel-based self-fluxing alloy has Hv550~
Since it has a high hardness of 800, which is close to the hardness of chromium oxide (CrzO3) HV2O3-1200, it is suitable for forming a wear-resistant surface layer as a binder for chromium oxide powder.
本発明で使用するニッケル基自溶合金は、JIS H
8303r自溶合金溶射」に規定されているMSFNi
l、MSFNi2、MSFNi3、MSFNi4、MS
FNi5のいずれも使用することができるが、硼素2〜
4重量%(以下、重量%を単に「%」で示す。)、珪素
2〜5%のものが好適である。硼素及び珪素は、いずれ
も2%未満では形成される表面層の硬度が低く、耐摩耗
性改善の効果が顕著ではなく、硼素が4%を越えると、
また珪素が5%を越えると、形成される表面層が硬くな
り過ぎ、かつ脆くなって耐摩耗性が却って劣化し、また
相手の摺動材料を摩耗させたりするようになる。従って
、硼素は2〜4%、珪素は2〜5%の範囲とするのが良
い。The nickel-based self-fluxing alloy used in the present invention is JIS H
MSFNi specified in 8303r Self-Fusing Alloy Thermal Spraying
l, MSFNi2, MSFNi3, MSFNi4, MS
Any of FNi5 can be used, but boron2~
4% by weight (hereinafter, weight% is simply expressed as "%") and 2 to 5% silicon is suitable. If both boron and silicon are less than 2%, the hardness of the surface layer formed will be low and the effect of improving wear resistance will not be significant, and if boron exceeds 4%,
If the silicon content exceeds 5%, the surface layer formed becomes too hard and brittle, resulting in poor wear resistance and abrasion of the mating sliding material. Therefore, the boron content is preferably in the range of 2 to 4%, and the silicon content is in the range of 2 to 5%.
本発明で使用するニッケル基自溶合金としては、例えば
、10〜20%クロム、2〜4%硼素、2〜5%珪素、
0.1〜1%炭素、残部が実質的にニッケルからなる市
販のもので良い。The nickel-based self-fluxing alloy used in the present invention includes, for example, 10 to 20% chromium, 2 to 4% boron, 2 to 5% silicon,
A commercially available material consisting of 0.1 to 1% carbon and the remainder substantially nickel may be used.
本発明に基く摺動部材の表面層は、1〜74μmの粒径
を有する炭化クロム粉末粒子の表面に、微細な上記化学
組成のニッケル基自溶合金粉末を樹脂等をバインダとし
て被覆したものをプラズマ溶射して形成される。また上
記酸化クロム粉末と上記自溶合金粉末とを混合し、造粒
した造粒粉をプラズマ溶射しても良い。これら造粒粉の
粒径は、5μm未満ではプラズマジェット流に投入する
ことが困難であり、105 μmを越えると溶射中に熔
融しきれなくなることがあるので、5〜105μmの範
囲とするのが望ましい。上記ニッケル基自溶合金は、溶
射表面層中でネットワーク状を呈して結合力を高めるの
であるが、原料粉を上記のような造粒粉によらず、酸化
クロム粉と自溶合金粉との単純な混合粉を使用すると、
両者の粒径や比重の差に起因して均一な溶射表面層が得
られ難く、即ち、自溶合金が全面にはネットワーク状に
ならず1.自溶合金による結合力が得られ難くなる。The surface layer of the sliding member according to the present invention is made by coating the surface of chromium carbide powder particles having a particle size of 1 to 74 μm with fine nickel-based self-fluxing alloy powder having the above chemical composition using a resin or the like as a binder. Formed by plasma spraying. Alternatively, the chromium oxide powder and the self-fluxing alloy powder may be mixed and granulated, and then the granulated powder may be plasma sprayed. If the particle size of these granulated powders is less than 5 μm, it is difficult to introduce it into the plasma jet stream, and if it exceeds 105 μm, it may not be completely melted during thermal spraying. desirable. The above-mentioned nickel-based self-fluxing alloy exhibits a network shape in the sprayed surface layer and increases the bonding strength. Using a simple flour mix,
Due to the difference in particle size and specific gravity between the two, it is difficult to obtain a uniform sprayed surface layer, that is, the self-fluxing alloy does not form a network over the entire surface.1. It becomes difficult to obtain the bonding strength of the self-fluxing alloy.
上記ニッケル基自溶合金の量は、10%未満では結合力
に寄与する効果が顕著ではなく、50%を越えると酸化
クロム粉末の量が少なくなって耐摩耗性、耐焼付性改善
の効果が不充分となるので、10〜50%の範囲とする
。If the amount of the above-mentioned nickel-based self-fluxing alloy is less than 10%, the effect contributing to bonding strength will not be significant, and if it exceeds 50%, the amount of chromium oxide powder will decrease and the effect of improving wear resistance and seizure resistance will be reduced. Since it is insufficient, it is set in the range of 10 to 50%.
ホ、実施例 以下に実施例を挙げて本発明を具体的に説明する。E, Example The present invention will be specifically explained below with reference to Examples.
5mmX5++nX10n+の角柱状鋳鉄試料を多数用
意し、その正方形端面に下記第1表に示す材料をプラズ
マ溶射して厚さ0.3鶴の溶射表面層を形成した。但し
、■は酸素−アセチレン爆射、Jはめっきによった。A large number of prismatic cast iron samples measuring 5 mm x 5 + n x 10 n + were prepared, and the materials shown in Table 1 below were plasma sprayed onto the square end faces of the samples to form a sprayed surface layer with a thickness of 0.3 mm. However, ■ is by oxygen-acetylene bombardment, and J is by plating.
第 1 表
同表中、C,D及びEが本発明に基づく耐摩耗性表面層
試験片である。Aは酸化クロムのみ、Bは本発明の範囲
を外れて自溶合金の量が少ないもの、Fは本発明の範囲
を外れて自溶合金の量が多いもので、A、B、、F、G
、H及びIは比較の試験片である。Table 1 In the same table, C, D and E are wear-resistant surface layer test pieces based on the present invention. A is only chromium oxide, B is outside the scope of the present invention and has a small amount of self-fluxing alloy, F is outside the scope of the present invention and has a large amount of self-fluxing alloy. G
, H and I are comparison specimens.
なお、酸化クロムは粒径10〜53μm、自溶合金は、
この酸化クロム粉粒子の表面を被覆していて、化学組成
は11.5%Cr 、 3.0%B、3.4%St、0
.4%C1残部実質的にNiである。In addition, chromium oxide has a particle size of 10 to 53 μm, and self-fluxing alloy has a particle size of 10 to 53 μm.
The surface of this chromium oxide powder particle is coated with a chemical composition of 11.5% Cr, 3.0% B, 3.4% St, 0
.. The balance of 4% C1 is essentially Ni.
これら試験片の上記表面層表面を0.8〜1.5μmの
表面粗さに研摩仕上げし、摩耗試験及び焼付試験に供し
た。摺動相手材としては、最近、セラミックスがその優
れた耐摩耗性の故に注目されており、所謂セラミックエ
ンジンの開発が試みられていることに鑑み、常圧焼結さ
れた炭化珪素(α−3i C)又は窒化珪素(Si3N
4)を選んだ。The surfaces of the surface layers of these test pieces were polished to a surface roughness of 0.8 to 1.5 μm, and subjected to wear tests and seizure tests. Ceramics have recently been attracting attention as sliding mating materials due to their excellent wear resistance, and in view of the fact that attempts are being made to develop so-called ceramic engines, pressureless sintered silicon carbide (α-3i C) or silicon nitride (Si3N
I chose 4).
これら摺動相手材の摺動面は0.8〜1.5μmの表面
粗さに研摩仕上げを施した。The sliding surfaces of these sliding mating materials were polished to a surface roughness of 0.8 to 1.5 μm.
本発明に基づく耐摩耗性表面層試験片の顕微鏡組織のス
ケッチ(倍率400倍)を試験片Eを例に挙げて第1図
に示す。試験片5は、鋳鉄母材5c、溶射表面層の密着
性を良好にするために設けたニッケルーアルミニウムの
下地溶射層5b及び溶射表面層5aからなっている。溶
射表面層5aは、酸化クロム粒子5dとこれを囲んでネ
ットワーク状を呈する自溶合金5eとからなり、気孔5
rをDの作成に使用した溶射原料粉の走査型電子顕微鏡
による二次電子像(倍率2000倍)の写真である。A sketch (400x magnification) of the microscopic structure of a wear-resistant surface layer test piece according to the present invention is shown in FIG. 1, taking test piece E as an example. The test piece 5 consists of a cast iron base material 5c, a nickel-aluminum base sprayed layer 5b provided to improve the adhesion of the sprayed surface layer, and a sprayed surface layer 5a. The sprayed surface layer 5a is composed of chromium oxide particles 5d and a self-fluxing alloy 5e surrounding them in a network shape, and has pores 5.
This is a photograph of a secondary electron image (magnification: 2000 times) of the thermal spray raw material powder used to create r and D, taken with a scanning electron microscope.
(i)焼付試験
試験装置は第3図及び第3図のIV−IV線に沿う矢視
側面図である第3図に概要を図解的に示すものであって
、ステータホルダ1に取外し可能に取付けられた直径8
0mm、厚さ10+mの研磨仕上げを施した円板2の中
央には裏側から注油孔3を通じて潤滑油が注油される。(i) The seizure test test device is schematically shown in FIG. 3 and FIG. 3, which is a side view taken along line IV-IV in FIG. 3, and is detachable from the stator holder 1. installed diameter 8
Lubricating oil is applied to the center of the polished disk 2 with a thickness of 0 mm and a thickness of 10+ m through an oil filling hole 3 from the back side.
ステータホルダ1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
にしである。A pressing force P is applied to the stator holder 1 by a hydraulic device (not shown) at a predetermined pressure toward the right in the figure.
円板2に相対向してロータ4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である。ロータ
4の円板2に対する端面に取付けられた試験片保持具4
aには正方形端面(この例では第1図の5aの表面)を
摺動面として試験片5が同心円上に等間隔に4個取外し
可能に、かつ円板2に対して摺動自在に取付けである。A rotor 4 is provided opposite to the disk 2, and is rotated at a predetermined speed by a drive device (not shown). Test piece holder 4 attached to the end face of the rotor 4 relative to the disk 2
On a, four test pieces 5 are removably attached at equal intervals on a concentric circle with the square end face (in this example, the surface 5a in FIG. 1) as a sliding surface, and are slidable on the disk 2. It is.
このような装置において、ステータ1に所定の押圧力P
をかけ、所定の面圧で円板(相手材)2と試験片5とが
接触するようにしておいて、注油孔3から摺動面に所定
給油速度で給油しながらロータ4を回転させる。一定時
間毎にステータ1に作用する圧力を階段的に増加してゆ
き、ロータ4の回転によって試験片5と相手の円板2と
の摩擦によってステータ1に生ずるトルク(摩擦力によ
って生ずるトルク)Tをスピンドル6を介してロードセ
ル7に作用せしめ、その変化を動歪計8で読取り、記録
計9に記録される。トルクTが急激に上昇するときに焼
付が生じたものとし、その大小を以て耐焼付性の良否を
判断する。In such a device, a predetermined pressing force P is applied to the stator 1.
The test piece 5 is brought into contact with the disc (mate material) 2 under a predetermined surface pressure, and the rotor 4 is rotated while lubricating the sliding surface from the lubricating hole 3 at a predetermined lubricating speed. The pressure acting on the stator 1 is increased stepwise at regular intervals, and the torque (torque generated by frictional force) generated on the stator 1 due to the friction between the test piece 5 and the mating disk 2 due to the rotation of the rotor 4 is T. is applied to the load cell 7 via the spindle 6, and the change is read by the dynamic strain meter 8 and recorded on the recorder 9. It is assumed that seizure has occurred when the torque T increases rapidly, and the quality of the seizure resistance is determined based on the magnitude of the increase.
試験条件は次に示す通りである。The test conditions are as follows.
摩擦速度= 8 m 156(
潤滑油:モータオイル5AE30を2ml/min給油
接触圧カニ試験開始時20 kg / c++t、その
後3分間経過毎に10 kg / crlづつ上昇相手
円板材料:常圧焼結されたα−3iC又はSi3N4
試験結果は下記第2表に示す通りである。Friction speed = 8 m 156 (Lubricating oil: Motor oil 5AE30 at 2 ml/min Lubricating contact pressure 20 kg/c++t at the start of the crab test, increasing by 10 kg/crl every 3 minutes thereafter) Mating disc material: Normal pressure sintering The α-3iC or Si3N4 test results are shown in Table 2 below.
第 2 表
同表から、本発明に基づ(耐摩耗性表面層試験片C,D
、Eは、比較の試験片F−Jに較べて耐焼付性が明らか
に改善されていることが解る。比較の試験片A及びBは
、本発明に基づく耐摩耗性表面層試験片C,D、Eと略
同程度の焼付発生面圧を示したが、A、B共に試験後、
摺動面に亀甲状の亀裂が観察されたのに対し、C,D、
Eではこのような亀裂は観察されなかった。Table 2 From the same table, based on the present invention (wear-resistant surface layer test pieces C, D
It can be seen that the seizure resistance of specimens F and E is clearly improved compared to comparative specimen F-J. Comparative test pieces A and B showed approximately the same surface pressure at which seizure occurred as the wear-resistant surface layer test pieces C, D, and E based on the present invention, but both A and B showed that after the test,
While tortoiseshell-shaped cracks were observed on the sliding surface, C, D,
No such cracks were observed in E.
(11)摩耗試験
試験装置は概要を第5図に示すものであって、管状電気
炉13中にはα−3iCの円筒焼結体(外径70鶴、内
径30龍、長さ7(lna、外周面は表面粗さ0.8〜
1.5μmに研摩仕上げ)12が炉外に設置された図示
しない駆動装置によって所定速度で回転可能に設置され
ている。同図中、13aは炉芯管、13bは抵抗発熱体
、13cは断熱材である。円筒体12の外周面に溶射表
面層5aが摺接するように、前記試験片5がレバー11
に取付けられている。レバー11は、両端が電気炉13
外に突出しており、その一端を支点とし、他の一端に図
示しない重錘が取付けられ、試験片5が所定面圧で円筒
体12に接触するようにしである。(11) The outline of the wear test test apparatus is shown in FIG. , the outer peripheral surface has a surface roughness of 0.8~
(Polished to 1.5 μm) 12 is rotatably installed at a predetermined speed by a drive device (not shown) installed outside the furnace. In the figure, 13a is a furnace core tube, 13b is a resistance heating element, and 13c is a heat insulating material. The test piece 5 is attached to the lever 11 so that the sprayed surface layer 5a is in sliding contact with the outer peripheral surface of the cylindrical body 12.
installed on. The lever 11 has electric furnaces 13 at both ends.
It protrudes outward, with one end serving as a fulcrum and a weight (not shown) attached to the other end, so that the test piece 5 contacts the cylindrical body 12 with a predetermined surface pressure.
このような装置を使用して、電気炉13内の温度を35
0℃に保持し、接触荷重5kg(面圧20kg/cfl
I)、摩擦速度0.5m/5eC1摩擦距離1.3km
、無潤滑の条件で試験を行った。Using such a device, the temperature inside the electric furnace 13 can be increased to 35%.
Maintained at 0℃, contact load 5kg (surface pressure 20kg/cfl
I), friction speed 0.5m/5eC1 friction distance 1.3km
, the test was conducted under non-lubricated conditions.
試験結果は第6図に示す通りである。摩耗量は、試験片
5については摩耗体積で、相手円筒体12については摩
耗によって外周面に生じた管状痕の半径方向断面積で示
しである。The test results are shown in FIG. The amount of wear is shown by the wear volume for the test piece 5, and by the radial cross-sectional area of a tubular mark produced on the outer circumferential surface due to wear for the mating cylindrical body 12.
第6図から、本発明に基づく耐摩耗性表面層試験片C,
D及びEは比較の試験片F、GSH,I、Jに較べて摩
耗量が少ないことが解る。また、試験後の摺動面は滑ら
かであった。比較の試験片■、Jの異状摩耗は、溶射表
面層又はめっき層が消失して摩耗が鋳鉄母材にまで及ん
でいることを表わしている。比較の試験片A及びBは、
摩耗量は少なく表われているが、摺動面の一部に溶射表
面層の剥離が観察され、また、相手材の摩耗が多い。From FIG. 6, wear-resistant surface layer test piece C based on the present invention,
It can be seen that D and E have less wear than comparative test pieces F, GSH, I, and J. Furthermore, the sliding surface was smooth after the test. The abnormal wear of comparative test pieces ① and J indicates that the thermal sprayed surface layer or the plating layer has disappeared and the wear has extended to the cast iron base material. Comparative test pieces A and B are
Although the amount of wear appears to be small, peeling of the sprayed surface layer was observed on a part of the sliding surface, and there was a lot of wear on the mating material.
自身の摩耗、相手材の摩耗共に少ないのは試験片CSD
及びEである。Test piece CSD has less wear both on itself and on the other material.
and E.
へ、発明の詳細
な説明したように、本発明に基づく耐摩耗性表面層は、
結合材としてのニッケル基自溶合金が10〜50%、残
部が粒径1〜74μmの酸化クロム粉末から実質的にな
る構成としであるので、硬質の酸化クロム粒子がネット
ワーク状を呈する硬質のニッケル基自溶合金によって強
固に結合された組織となっている。その結果、耐焼付性
が著しく改善され、その上、高温、無潤滑のような苛酷
な摺動条件下でも優れた耐摩耗性を示し、耐久性が大幅
に改善される。As described in the detailed description of the invention, the wear-resistant surface layer according to the invention comprises:
The structure is made up of 10 to 50% nickel-based self-fluxing alloy as a binder, and the remainder is essentially chromium oxide powder with a particle size of 1 to 74 μm, so that hard nickel with a network of hard chromium oxide particles is formed. The structure is strongly bonded by the base self-fluxing alloy. As a result, seizure resistance is significantly improved, and in addition, it exhibits excellent wear resistance even under severe sliding conditions such as high temperatures and no lubrication, and durability is significantly improved.
従って、本発明に基づく耐摩耗性表面層を有する摺動部
材を使用するときは、機関のオーバーホールからの次の
オーバーホール塩の期間が大幅に延長され、本発明の産
業上の利用価値は大きい。Therefore, when using the sliding member having the wear-resistant surface layer according to the present invention, the period between engine overhauls and subsequent overhaul salts is greatly extended, and the industrial utility value of the present invention is great.
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図は耐摩耗性表面層の顕微鏡組織のスケッチ、
第2図は溶射原料粉粒子の電子顕微鏡写真(二次電子像
)
第3図は焼付試験に使用した試験装置の要部を示す部分
断面図、
第4図は第3図のIV−IV線矢視側面図、第5図は摩
耗試験に使用した試験装置の要部断面図、
第6図は摩耗試験の結果を示すグラフ
である。
なお、図面に示された符号に於いて、
1・・・・・・・・・ステータ
2・・・・・・・・・相手円板
3・・・・・・・・・注油孔
4・・・・・・・・・ロータ
5・・・・・・・・・試験片
5a・・・・・・・・・溶射表面層
5b・・・・・・・・・下地溶射層
5c・・・・・・・・・鋳鉄母材
5d・・・・・・・・・酸化クロム粒子5e・・・・・
・・・・ニッケル基自溶合金5f・・・・・・・・・気
孔
7・・・・・・・・・ロードセル
8・・・・・・・・・動歪計
9・・・・・・・・・記録計
11・・・・・・・・・レバー
12・・・・・・・・・相手円筒体
13・・・・・・・・・管状電気炉
である。The drawings all show examples of the present invention. Figure 1 is a sketch of the microscopic structure of the wear-resistant surface layer, and Figure 2 is an electron micrograph (secondary electron image) of thermal spray raw material powder particles. Figure 3 is a partial sectional view showing the main parts of the test equipment used in the seizure test, Figure 4 is a side view taken along the line IV-IV in Figure 3, and Figure 5 is the main part of the test equipment used in the wear test. The cross-sectional view and FIG. 6 are graphs showing the results of the wear test. In addition, in the symbols shown in the drawings, 1...Stator 2...Mating disk 3...Oil filling hole 4. ......Rotor 5...Test piece 5a...Thermal sprayed surface layer 5b...Thermal sprayed base layer 5c... ......Cast iron base material 5d...Chromium oxide particles 5e...
...Nickel-based self-fluxing alloy 5f...Pore 7...Load cell 8...Dynamic strain meter 9... . . . Recorder 11 . . . Lever 12 . . . Matching cylindrical body 13 . . . A tubular electric furnace.
Claims (1)
量%、残部が粒径1〜74μmの酸化クロム粉末から実
質的になる耐摩耗性表面層。1. A wear-resistant surface layer consisting essentially of 10 to 50% by weight of a nickel-based self-fluxing alloy as a binder, and the remainder consisting of chromium oxide powder with a particle size of 1 to 74 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60072343A JPS61231154A (en) | 1985-04-04 | 1985-04-04 | Wear resisting surface layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60072343A JPS61231154A (en) | 1985-04-04 | 1985-04-04 | Wear resisting surface layer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61231154A true JPS61231154A (en) | 1986-10-15 |
JPH0235026B2 JPH0235026B2 (en) | 1990-08-08 |
Family
ID=13486556
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60072343A Granted JPS61231154A (en) | 1985-04-04 | 1985-04-04 | Wear resisting surface layer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61231154A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013144833A (en) * | 2012-01-16 | 2013-07-25 | Shimane Prefecture | Ceramic spraying material, forming method for ceramic spraying film, and functional ceramic spraying film |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS529635A (en) * | 1975-07-11 | 1977-01-25 | Eutectic Corp | Abrasionnresistant coating containing tungsten carbide |
-
1985
- 1985-04-04 JP JP60072343A patent/JPS61231154A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS529635A (en) * | 1975-07-11 | 1977-01-25 | Eutectic Corp | Abrasionnresistant coating containing tungsten carbide |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013144833A (en) * | 2012-01-16 | 2013-07-25 | Shimane Prefecture | Ceramic spraying material, forming method for ceramic spraying film, and functional ceramic spraying film |
Also Published As
Publication number | Publication date |
---|---|
JPH0235026B2 (en) | 1990-08-08 |
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