JPS6315987B2 - - Google Patents
Info
- Publication number
- JPS6315987B2 JPS6315987B2 JP55068175A JP6817580A JPS6315987B2 JP S6315987 B2 JPS6315987 B2 JP S6315987B2 JP 55068175 A JP55068175 A JP 55068175A JP 6817580 A JP6817580 A JP 6817580A JP S6315987 B2 JPS6315987 B2 JP S6315987B2
- Authority
- JP
- Japan
- Prior art keywords
- primary
- particles
- sliding member
- wear
- silicon
- 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.)
- Expired
Links
- 239000011856 silicon-based particle Substances 0.000 claims description 36
- 239000000463 material Substances 0.000 claims description 31
- 239000002245 particle Substances 0.000 claims description 10
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 claims description 9
- 229910000838 Al alloy Inorganic materials 0.000 claims description 7
- 239000011159 matrix material Substances 0.000 claims description 6
- 239000007921 spray Substances 0.000 description 19
- 239000000843 powder Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000000758 substrate Substances 0.000 description 11
- 238000007751 thermal spraying Methods 0.000 description 10
- 230000013011 mating Effects 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- 229910000676 Si alloy Inorganic materials 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 239000000956 alloy Substances 0.000 description 5
- 238000004512 die casting Methods 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 238000005242 forging Methods 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- 239000010962 carbon steel Substances 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000005496 eutectics Effects 0.000 description 2
- 239000012208 gear oil Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 229910021419 crystalline silicon Inorganic materials 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 238000007750 plasma spraying Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 102220259718 rs34120878 Human genes 0.000 description 1
- 102200082816 rs34868397 Human genes 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/067—Metallic material containing free particles of non-metal elements, e.g. carbon, silicon, boron, phosphorus or arsenic
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Pistons, Piston Rings, And Cylinders (AREA)
- Coating By Spraying Or Casting (AREA)
Description
本発明はシフトフオーク爪部、シリンダライナ
ー内面、ピストンリング、シンクロナイザーリン
グ内面、ミツシヨン摩擦板等に使用しうる摺動部
材に関するものである。
過共晶ケイ素アルミニウム合金は優れた耐摩耗
性を有することから、各種の摺動部材に適用され
ている。この合金はアルミニウム−ケイ素の共晶
組織に初晶のケイ素粒子が分散したもので、この
初晶ケイ素粒子の存在が耐摩耗性に大きく寄与し
ていることは、初晶ケイ素粒子の存在しない亜共
晶アルミニウム−ケイ素合金との耐摩耗性の比較
から明らかである。
しかしながら、逆にこの初晶ケイ素粒子の存在
には摺動部材として好ましくない面もある。すな
わち、初晶ケイ素粒子による相手材攻撃性の問題
である。初晶ケイ素粒子はビツカース硬度1000程
度の硬質物であるため、摩擦中にマトリツクスの
方が選択的に早く摩耗し、初晶ケイ素(Si)粒子
が摺動部材の表面に浮出して、相手材を摩耗させ
易い。摩耗がさらに進行すると表面部に浮出した
初晶Si粒子がマトリツクスから剥落することがあ
り、このような状態のときには相手材の摩耗はさ
らに激しくなる。
また、これに関して、初晶ケイ素粒子が存在す
ると刃具を摩耗させるので、摺動部材製造上の大
きな障害となつている。
上記の問題を解決するためには、初晶Si粒子の
サイズを細かくして、マトリツクスからの浮出し
や剥落を抑え、且つ、粒子自体の相手攻撃性を減
じると共に、初晶Si粒子量が過剰にならないよう
にすることも必要である。従来このための具体的
な方法として、鋳造、ダイカスト、鍛造等のあ
と、冷却速度を速めて、初晶Si粒子の微細化をは
かることが行なわれているが、20μ以下の微細な
粒子径を得るための実用的方法は知られていな
い。また、溶射法や合金ピース法など、摺動部に
のみ過共晶ケイ素アルミニウム合金を形成させる
方法では、前記の鋳造、ダイカスト、鍛造等の一
体製品化法に比較すれば冷却速度を高めることが
できるが、それでも粒子を10μ以下の充分微細な
サイズにすることは従来不可能であつた。
本発明は上記の問題を解決するためのもので、
過共晶ケイ素アルミニウム合金の初晶Si粒子を微
細化させることによつて、相手材への攻撃性が少
なく、且つ、耐摩耗性、耐焼付性に優れ、さらに
切削が容易で経済的に生産可能な摺動部材を提供
するものである。
本発明の摺動部材は、鉄系金属または軽金属を
基材とする摺動面に、粒径5μ以下の初晶Si粒子を
マトリツクス中に面積率で2〜20%分散させた過
共晶ケイ素アルミニウム合金の溶射層を、50μ以
上の厚さに設けたことを特徴とする。
本発明摺動部材において、初晶Si粒子径を5μ以
下に規定したのは、後記実施例1で摩耗試験例を
もつて説明するとおり、この径が小さい方が相手
材に対する攻撃性が小さくなり、切削性等も良好
になるため5μ以下とした。
初晶Si粒子の面積率を2〜20%に規定したの
は、2%以下では溶射層の耐摩耗性が得られず、
他方20%以上になると溶射層の耐焼付性が悪くな
るので、これらの弊害を防ぐため2〜20%とし
た。
溶射層の厚さを50μ以上に規定したのは、通常
の溶射層表面には30〜50μの凹凸があるため、充
分な厚さに溶射しないと基材の露出が起つたり、
溶射層と基材との接着力が弱くなるので50μ以上
とした。
本発明の摺動部材を製造するには、例えば、好
ましくはケイ素含有量15〜30%の過共晶ケイ素合
金材料を、溶射ガンから基材に溶射される間に該
合金の融点以上の温度に加熱して完全に溶融さ
せ、この溶融物を好ましくは300℃以下の温度に
保つた基材に溶射することによつて製造すること
ができる。
上記の方法において、ケイ素含有量15〜30%の
過共晶ケイ素合金材料を使用することが好ましい
理由は、初晶Si面積率2〜20%の溶射層を容易に
得ることができるためである。
また、溶射材料(過共晶ケイ素合金)を未溶融
分が残存した状態のままで使用すると、得られた
溶射層の初晶Si粒子が充分微細化されないばかり
でなく、溶射層自体の強さも劣る結果となり易い
ので、溶射材料は完全に溶融してから使用するこ
とが望ましい。
溶射材料は粉末、ワイヤのいずれの状態のもの
でも使用できるが、アトマイズ法で製造した粉末
状のものを用いれば、アトマイズによつて初晶Si
粒子が予め比較的細かく20〜30μ以下にされるた
め、容易に溶融できて都合がよい。
さらに、溶射される基材の温度が高いと溶融物
の冷却速度が遅くなり、初晶Si粒子を充分微細化
できなくなるので、基材の温度を300℃以下にし
て溶射すると都合がよい。
溶射法としては、ガス溶線式、ガス粉末式、プ
ラズマ式、爆発式等のいずれの方法を使用しても
よいが、熱エネルギーがフレーム部分に高度に集
中したプラズマ式溶射方法を使用すれば、高温の
フレーム部分で溶射材料は充分に溶融し、フレー
ム部分を離れれば急速に冷却するので、初晶Si粒
子の微細化した溶射層を得るために有利である。
以下本発明につき実施例により詳細に説明する
が、本発明はこれらの実施例のみに限定されるも
のではない。
実施例 1
溶射材料として、アトマイズ法により、粒度
100〜400メツシユ、ケイ素含有量23.9%のアルミ
ニウムケイ素合金粉末を作製した。得られれた粉
末の初晶Si粒子径は3〜25μ、初晶Si面積率は10
〜12%、ビツカース硬さ(荷重300g)は130〜
145であつた。
この溶射材料をメトコ(METCO)社製3M型
プラズマ溶射装置により、120mmの溶射距離から、
各種温度に保持した寸法30×30×5mmの炭素鋼
S45C板状試験片(基材)に、200μの厚さに溶射
して、第1表に示す本発明および本発明外の摺動
部材よりなる板状試験片を作製した。プラズマガ
スはN270.8/分、H24.7/分を使用し、基材
の温度の調節は溶射開始前に基材を予熱し、溶射
中は冷却制御して行なつた。第1表中摺動部材の
記号をマルで囲んだものは本発明の摺動部材、そ
の他は本発明外の摺動部材である。
得られた摺動部材の溶射層の特性として、初晶
Si粒径、初晶Si面積率およびビツカース硬さを調
べ、溶射条件との関係を調査した。これらの値も
第1表に示す。
The present invention relates to a sliding member that can be used for a shift fork pawl, an inner surface of a cylinder liner, a piston ring, an inner surface of a synchronizer ring, a transmission friction plate, etc. Hypereutectic silicon-aluminum alloys have excellent wear resistance and are therefore used in various sliding members. This alloy has primary silicon particles dispersed in an aluminum-silicon eutectic structure, and the presence of these primary silicon particles contributes greatly to wear resistance. This is clear from the comparison of wear resistance with a eutectic aluminum-silicon alloy. However, conversely, the presence of these primary silicon particles has some aspects that are undesirable as a sliding member. In other words, there is a problem of the aggressiveness of the primary silicon particles to the other material. Because primary silicon particles are hard with a Vickers hardness of about 1000, the matrix selectively wears out faster during friction, and the primary silicon (Si) particles stand out on the surface of the sliding member, causing damage to the sliding member. Easy to wear out the material. As the wear progresses further, the primary Si particles floating on the surface may peel off from the matrix, and in such a state, the wear of the mating material becomes even more severe. In addition, in this regard, the presence of primary silicon particles causes wear of the cutting tool, which is a major obstacle in the production of sliding members. In order to solve the above problems, it is necessary to reduce the size of primary Si particles to suppress their extrusion and peeling from the matrix, reduce the aggressiveness of the particles themselves, and reduce the amount of primary Si particles. It is also necessary to avoid excessive amounts. Conventionally, a specific method for this purpose has been to increase the cooling rate after casting, die casting, forging, etc. in order to make the primary Si particles finer. There is no known practical method for obtaining it. Additionally, methods such as thermal spraying and alloy piece methods that form a hypereutectic silicon-aluminum alloy only on sliding parts can increase the cooling rate compared to the above-mentioned integrated product methods such as casting, die casting, and forging. However, it has previously been impossible to make the particles sufficiently fine, less than 10 μm in size. The present invention is intended to solve the above problems,
By making the primary Si particles of the hypereutectic silicon-aluminum alloy fine, it is less aggressive to the mating material, has excellent wear resistance and seizure resistance, and is easy to cut and economically produced. This provides a possible sliding member. The sliding member of the present invention is made of hypereutectic silicon in which primary Si particles with a particle size of 5 μm or less are dispersed in an area ratio of 2 to 20% in a matrix on a sliding surface made of iron-based metal or light metal. It is characterized by having a sprayed aluminum alloy layer with a thickness of 50μ or more. In the sliding member of the present invention, the primary Si particle diameter is specified to be 5μ or less, as will be explained later in Example 1 with a wear test example. In order to improve machinability, etc., the thickness was set to 5μ or less. The reason why the area ratio of primary Si particles was specified to be 2 to 20% is because if it is less than 2%, the wear resistance of the sprayed layer cannot be obtained.
On the other hand, if it exceeds 20%, the seizure resistance of the sprayed layer will deteriorate, so in order to prevent these disadvantages, the content is set at 2 to 20%. The reason why we specified the thickness of the sprayed layer to be 50μ or more is because the surface of a normal sprayed layer has irregularities of 30 to 50μ, so if it is not sprayed to a sufficient thickness, the base material may be exposed.
Since the adhesion between the sprayed layer and the base material becomes weak, the thickness was set to 50μ or more. To manufacture the sliding member of the present invention, for example, a hypereutectic silicon alloy material preferably having a silicon content of 15 to 30% is sprayed onto a substrate from a thermal spray gun at a temperature above the melting point of the alloy. It can be produced by heating to completely melt it and spraying the melt onto a substrate preferably maintained at a temperature below 300°C. In the above method, the reason why it is preferable to use a hypereutectic silicon alloy material with a silicon content of 15 to 30% is that a sprayed layer with a primary Si area ratio of 2 to 20% can be easily obtained. . In addition, if the thermal spray material (hypereutectic silicon alloy) is used with unmelted components remaining, not only will the primary Si particles in the resulting thermal spray layer not be sufficiently refined, but the strength of the thermal spray layer itself will deteriorate. It is desirable to completely melt the thermal spray material before use, as poor results are likely to occur. Thermal spray materials can be used in either powder or wire form, but if powdered materials manufactured by the atomization method are used, primary Si crystals can be formed by atomization.
Since the particles are made relatively fine in advance to a size of 20 to 30 μm or less, they can be easily melted, which is convenient. Furthermore, if the temperature of the substrate to be thermally sprayed is high, the cooling rate of the melt will be slow, making it impossible to sufficiently refine the primary Si particles, so it is convenient to thermally spray the substrate at a temperature of 300° C. or lower. Any of the following thermal spraying methods may be used: gas wire, gas powder, plasma, and explosion methods. The sprayed material is sufficiently melted in the high-temperature frame portion, and cools rapidly once it leaves the frame portion, which is advantageous for obtaining a sprayed layer containing fine primary Si particles. EXAMPLES The present invention will be explained in detail below with reference to Examples, but the present invention is not limited to these Examples. Example 1 As a thermal spray material, the particle size was
An aluminum-silicon alloy powder with 100 to 400 meshes and a silicon content of 23.9% was prepared. The primary Si particle size of the obtained powder was 3 to 25μ, and the area ratio of primary Si was 10.
~12%, Bitskers hardness (load 300g) is 130~
It was 145. This thermal spraying material was sprayed from a spraying distance of 120mm using a METCO 3M plasma spraying device.
Carbon steel with dimensions 30 x 30 x 5 mm kept at various temperatures
A S45C plate-shaped test piece (substrate) was thermally sprayed to a thickness of 200μ to produce plate-shaped test pieces made of sliding members of the present invention and non-inventive sliding members shown in Table 1. Plasma gas used was N 2 70.8/min and H 2 4.7/min, and the temperature of the substrate was controlled by preheating the substrate before starting thermal spraying and controlling cooling during thermal spraying. In Table 1, the sliding members whose symbols are circled are the sliding members of the present invention, and the others are sliding members other than the present invention. As a characteristic of the sprayed layer of the obtained sliding member, the primary crystal
The Si particle size, primary Si area ratio, and Vickers hardness were investigated, and the relationship with thermal spraying conditions was investigated. These values are also shown in Table 1.
【表】
○ 本発明摺動部材
第1表に示した溶射条件と溶射層の特性の関係
から次のことが判る。
(1) 溶射材料粉末の粒度が細かいほど、溶射電流
が大きいほど、そして粉末供給速度が小さいほ
ど、初晶Si粒子の小さい溶射層を有する摺動部
材が得られる。
(2) 基材温度が低い方が溶射層の初晶Si粒子が微
細化され易く、基材温度が400℃以上のときは
初晶Si粒子は充分微細化しない。
(3) (1)、(2)を総合して考えると、溶射材料粉末が
充分溶融しており、基材温度が低い(すなわ
ち、溶射材料の冷却が早い)場合に、Si粒子が
より微細化した溶射層が得られる。
(4) 初晶Si粒子の微細化が進んだ溶射層では、層
中の初晶Si面積率が若干減少する。これは微細
化が進んだ時に晶出中の冷却効果が大きかつた
ため、晶出しないSiがあつたためと考えられ
る。
(5) 溶射層の硬さは基材温度が低い時ほど高くな
る。
なお、上記で製造した摺動部材の代表例とし
て、本発明の摺動部材Wおよび本発明外の摺動部
材Gの溶射層断面組織の顕微鏡写真を、それぞれ
第1図および第2図に示す。第1図の本発明摺動
部材では初晶Si粒子径が全て5μ以下と細かいのに
対し、第2図の本発明外摺動部材では粒径5μ以
下およびそれよりはるかに粒径の大きい初晶Si粒
子が混在していることが判る。
次に上記摺動部材のうち、代表例としてG,
H,L,W,Xよりなる板状試験片を用いて摩耗
試験を行なつた。相手側試験片としては、
SCr420(JIS G4104)の浸炭焼入した円筒試験片
(内径φ20、外径φ25.6、長さ16mm)を用い、試験
条件は次のように設定して行なつた。
摩耗試験機……機械試験所式
摩擦摩耗試験機
すべり速度……2.4m/秒
潤 滑 油……低粘度ギアオイル
油 温……35〜45℃
面圧および時間
(1) 最初10分間面圧12.5Kg/cm2でなじみ運転す
る。
(2) その後面圧を2分間毎に12.5Kg/cm2づつ最大
250Kg/cm2まで上昇させる。
上昇途中で焼付いた場合は、その段階で試験
を終了する。
(3) 試験後板状試験片および相手試験片の摩耗重
量を求める。
この摩耗試験の結果を第2表に示す。また、
比較のため、上記溶射材料と同じ組成のアルミ
ニウムケイ素合金(Al−24%Si)でダイカス
ト法により同様の大きさに製造した摺動用板状
試験片についても摩耗試験を行なつた。その結
果も第2表に併記する。なお、ダイカスト法で
作製した試験片の初晶Si粒子径は12〜115μ、面
積率は13.6%であり、ビツカース硬さは125〜
136であつた。[Table] ○ Sliding member of the present invention From the relationship between the spraying conditions and the properties of the sprayed layer shown in Table 1, the following can be seen. (1) The finer the particle size of the spray material powder, the larger the spray current, and the lower the powder supply rate, the more a sliding member having a spray layer with smaller primary Si particles can be obtained. (2) The lower the substrate temperature is, the easier the primary Si particles in the sprayed layer are to be refined, and when the substrate temperature is 400°C or higher, the primary Si particles are not sufficiently refined. (3) Considering (1) and (2) together, if the thermal spray material powder is sufficiently melted and the substrate temperature is low (that is, the thermal spray material cools quickly), the Si particles will become finer. A thermally sprayed layer is obtained. (4) In the sprayed layer where the primary Si particles have become finer, the area ratio of primary Si in the layer decreases slightly. This is thought to be due to the fact that the cooling effect during crystallization was large as the size of the crystallization progressed, so that some Si that did not crystallize was exposed. (5) The hardness of the sprayed layer increases as the substrate temperature decreases. As representative examples of the sliding members manufactured above, micrographs of the cross-sectional structures of the sprayed layers of the sliding member W of the present invention and the sliding member G other than the present invention are shown in FIGS. 1 and 2, respectively. . In the sliding member of the present invention shown in Fig. 1, all the primary Si particles have a fine diameter of 5 μ or less, whereas in the sliding member of the present invention shown in Fig. 2, the primary Si particles have a particle size of 5 μ or less and much larger. It can be seen that crystalline Si particles are mixed. Next, among the above sliding members, G,
A wear test was conducted using plate-shaped test pieces made of H, L, W, and X. As the other side test piece,
The test conditions were set as follows using a carburized and quenched cylindrical specimen of SCr420 (JIS G4104) (inner diameter φ20, outer diameter φ25.6, length 16 mm). Wear tester: Mechanical laboratory type Friction and wear tester Sliding speed: 2.4 m/sec Lubricating oil: Low viscosity gear oil Temperature: 35 to 45°C Surface pressure and time (1) Surface pressure for the first 10 minutes: 12.5 Run at Kg/ cm2 . (2) Afterwards, increase the surface pressure to a maximum of 12.5Kg/ cm2 every 2 minutes.
Raise to 250Kg/cm 2 . If the product seizes during the ascent, the test will end at that stage. (3) After the test, determine the wear weight of the plate-shaped test piece and the mating test piece. The results of this wear test are shown in Table 2. Also,
For comparison, abrasion tests were also conducted on sliding plate specimens made of an aluminum-silicon alloy (Al-24%Si) having the same composition as the above-mentioned thermal sprayed material and manufactured to the same size by die-casting. The results are also listed in Table 2. In addition, the primary Si particle diameter of the test piece produced by the die-casting method is 12 to 115μ, the area ratio is 13.6%, and the Vickers hardness is 125 to 115μ.
It was 136.
【表】
第2表から明らかなように、初晶Si粒子径を5μ
以下にした本発明摺動部材L,W,Xよりなる板
状試験片は、耐焼付性、耐摩耗性(摺動部材自身
および特に相手材)が他の板状試験片よりはるか
に優れていた。
実施例 2
溶射材料のケイ素含有量と溶射層の特性の関係
を調べるため、ケイ素含有量10%、30%、35%の
溶射材料粉末を用いて、実施例1と同じ基材試験
片に、第1表の摺動部材Wと同じ粉末粒度および
溶射条件で溶射して、摺動部材を作製した。この
摺動部材につい実施例1と同じ条件で摩耗試験を
行なつた。このときの溶射材料粉末の特性、溶射
層の特性および摩耗試験の結果をまとめて第3表
に示す。[Table] As is clear from Table 2, the primary Si particle diameter is 5μ
The following plate-shaped test pieces made of the sliding members L, W, and X of the present invention are far superior in seizure resistance and wear resistance (of the sliding members themselves and especially the mating material) than other plate-shaped test pieces. Ta. Example 2 In order to investigate the relationship between the silicon content of the thermal spray material and the properties of the thermal spray layer, thermal spray material powders with a silicon content of 10%, 30%, and 35% were used on the same base material test piece as in Example 1. A sliding member was prepared by thermal spraying using the same powder particle size and thermal spraying conditions as the sliding member W in Table 1. A wear test was conducted on this sliding member under the same conditions as in Example 1. Table 3 summarizes the characteristics of the thermal spray material powder, the characteristics of the thermal spray layer, and the results of the wear test.
【表】
* 板状試験片摩耗重量(mg)
** 円筒(相手側)試験片摩耗重量(mg)
第3表から明らかなように、Si含有量が少なく
粉末時に初晶SiのないAl−10Si溶射材料から得
られる溶射層は、マトリツクス中に初晶Si粒子が
全く出現せず、耐焼付性は良好であるものの、耐
摩耗性には劣つていた。また、Al−15Si、Al−
30Si、Al−35Siの各溶射材料では、実施例1で
説明したように、充分溶融してから急速な冷却条
件で溶射すれば、Si量の多少に関係なく溶射層の
初晶Si粒子の微細化が可能で、耐焼付性、耐摩耗
性も良好であつた。但し、Al−35Siから得た溶
射層では、初晶Si粒子の微細化程度は他の溶射材
料の場合と同じであつたが、初晶Si量が多くな
り、面積率で21%となつたため、耐焼付性、耐摩
耗性が低下した。
したがつて、良好な特性の摺動部材を得るに
は、溶射材料のSi含有量を35%より低く、好まし
くは30%以下に抑えて、それにより溶射層の初晶
Si面積率を20%以下に抑えればよいことが伴つ
た。
実施例 3
機械構造用炭素鋼材(S55C)を鍛造して、シ
フトフオーク本体部分を製造し、摺動面に相当す
る爪部部分に、本発明例として実施例1の第1表
Wと同じ粉末、溶射条件で厚さ0.15mmの溶射層を
形成させた。このシフトフオークを自動車用駆動
変速装置に装着して、低粘度ギヤオイルを用いて
実機評価した。このときのシフトフオーク爪部の
摩耗量および相手材ハブスリーブの摩耗量を第4
表に示す。なお、比較例として、実施例1で記載
したダイカスト法による同組成のシフトフオーク
についても同様に評価した結果を第4表に併記す
る。[Table] * Wear weight of plate specimen (mg)
** Cylindrical (mating side) test piece wear weight (mg)
As is clear from Table 3, the thermal sprayed layer obtained from the Al-10Si thermal sprayed material with low Si content and no primary Si crystals in the powder form does not have any primary Si particles in the matrix, and has poor seizure resistance. Although good, the wear resistance was poor. Also, Al−15Si, Al−
As explained in Example 1, 30Si and Al-35Si thermal spray materials can be melted sufficiently and then thermally sprayed under rapid cooling conditions, so that the fine primary Si particles in the sprayed layer can be formed regardless of the amount of Si. The anti-seizure properties and abrasion resistance were also good. However, in the sprayed layer obtained from Al-35Si, although the degree of refinement of the primary Si particles was the same as in the case of other sprayed materials, the amount of primary Si particles increased and the area ratio was 21%. , seizure resistance, and wear resistance decreased. Therefore, in order to obtain a sliding member with good properties, the Si content of the sprayed material should be kept below 35%, preferably below 30%, thereby reducing the primary crystallization of the sprayed layer.
It was necessary to suppress the Si area ratio to 20% or less. Example 3 A shift fork main body part was manufactured by forging carbon steel material (S55C) for machine structural use, and the same powder as in Table 1 W of Example 1 was applied to the pawl part corresponding to the sliding surface as an example of the present invention. A thermal sprayed layer with a thickness of 0.15 mm was formed under thermal spraying conditions. This shift fork was attached to an automobile drive transmission and evaluated on an actual machine using low viscosity gear oil. At this time, the amount of wear on the shift fork pawl and the amount of wear on the mating hub sleeve
Shown in the table. As a comparative example, Table 4 also shows the results of a similar evaluation of a shift fork of the same composition produced by the die-casting method described in Example 1.
【表】
第4表より明らかなとおり、本発明の摺動部材
で爪部を形成したシフトフオークは、比較シフト
フオークに比べて耐摩耗性に著しく優れ、また相
手材の摩耗も著しく少なかつた。
以上の結果より明らかなように、本発明の摺動
部材は耐焼付性、耐摩耗性(相手材の摩耗も含め
て)に優れるものである。本明細書中では実施例
3においてシフトフオークに使用した例を示した
が、実施例1の結果等から明らかなように、本発
明の摺動部材はシリンダライナ内面、ピストンリ
ング、ミツシヨン摩擦板その他各種部品の摺動部
材としても有用である。特に従来過共晶ケイ素ア
ルミニウム合金を使用して作製されていた摺動
面、あるいはそのようにして作製したが機械特性
に問題があつた摺動面の部材として特に適する。
また相手攻撃性が低いので、切削加工性等が要求
される部品の摺動面を本発明の摺動部材で形成す
ることにより、工具摩耗の問題も著しく改善され
る。さらに、本発明の摺動部材は溶射法で製造す
るため、基材の自由度が大きくとれ、アルミ合
金、鋼、鋳鉄等各種の基材が使用できるので、基
材を適宜選択することによつて、生産性、強さ、
耐摩耗性等の要求に広範に対応できる利点を有す
る。[Table] As is clear from Table 4, the shift fork in which the claw portion was formed from the sliding member of the present invention had significantly better wear resistance than the comparative shift fork, and also had significantly less wear on the mating material. . As is clear from the above results, the sliding member of the present invention has excellent seizure resistance and wear resistance (including wear of the mating material). In this specification, an example in which the sliding member of the present invention is used in a shift fork is shown in Example 3, but as is clear from the results of Example 1, the sliding member of the present invention can be used on the inner surface of a cylinder liner, a piston ring, a transmission friction plate, etc. It is also useful as a sliding member for various parts. It is particularly suitable as a member for sliding surfaces conventionally manufactured using hypereutectic silicon-aluminum alloys, or sliding surfaces manufactured in such a manner but with problems in mechanical properties.
Furthermore, since the sliding member of the present invention is less likely to attack others, the problem of tool wear can be significantly improved by forming the sliding surfaces of parts that require good machinability, etc., with the sliding member of the present invention. Furthermore, since the sliding member of the present invention is manufactured using a thermal spraying method, there is a large degree of freedom in the base material, and various base materials such as aluminum alloy, steel, and cast iron can be used. productivity, strength,
It has the advantage of being able to meet a wide range of requirements such as wear resistance.
第1図は本発明の摺動部材の断面組織の顕微鏡
写真(×1000)、第2図は比較例の摺動部材の断
面組織の顕微鏡写真(×400)を表わす。
1……初晶ケイ素粒子(小)、2……初晶ケイ
素粒子(大)、3……気孔。
FIG. 1 shows a microscopic photograph (×1000) of the cross-sectional structure of the sliding member of the present invention, and FIG. 2 shows a microscopic photograph (×400) of the cross-sectional structure of the sliding member of the comparative example. 1...Primary silicon particles (small), 2...Primary silicon particles (large), 3...pores.
Claims (1)
イ素粒子をマトリツクス中に面積率で2〜20%分
散させた過共晶ケイ素アルミニウム合金溶射層
を、50μ以上の厚さに設けたことを特徴とする摺
動部材。1 A hypereutectic silicon-aluminum alloy sprayed layer with a thickness of 50 μm or more is provided on the surface of the sliding part of the base material, in which primary silicon particles with a particle size of 5 μm or less are dispersed in a matrix with an area ratio of 2 to 20%. A sliding member characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6817580A JPS56166368A (en) | 1980-05-22 | 1980-05-22 | Sliding member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6817580A JPS56166368A (en) | 1980-05-22 | 1980-05-22 | Sliding member |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56166368A JPS56166368A (en) | 1981-12-21 |
| JPS6315987B2 true JPS6315987B2 (en) | 1988-04-07 |
Family
ID=13366169
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6817580A Granted JPS56166368A (en) | 1980-05-22 | 1980-05-22 | Sliding member |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56166368A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4328619C2 (en) * | 1993-08-26 | 1995-08-10 | Peak Werkstoff Gmbh | Partially reinforced cast aluminum component and process for its production |
| DE19643029A1 (en) * | 1996-10-18 | 1998-04-23 | Bayerische Motoren Werke Ag | Method for coating an internal combustion engine component made of an aluminum alloy with silicon |
| DE19733204B4 (en) * | 1997-08-01 | 2005-06-09 | Daimlerchrysler Ag | Coating of a hypereutectic aluminum / silicon alloy, spray powder for their production and their use |
| DE19733205B4 (en) * | 1997-08-01 | 2005-06-09 | Daimlerchrysler Ag | Coating for a cylinder surface of a reciprocating engine of a hypereutectic aluminum / silicon alloy, spray powder for their production and their use |
| DE19841619C2 (en) | 1998-09-11 | 2002-11-28 | Daimler Chrysler Ag | Material wire for producing wear-resistant coatings from hypereutectic Al / Si alloys by thermal spraying and its use |
| DE10313957A1 (en) | 2002-06-27 | 2004-01-22 | Bwg Gmbh & Co. Kg | Method for coating a surface of a track component and track component |
-
1980
- 1980-05-22 JP JP6817580A patent/JPS56166368A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56166368A (en) | 1981-12-21 |
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