JPH042761A - Wear-resistant composite material and its manufacturing method - Google Patents
Wear-resistant composite material and its manufacturing methodInfo
- Publication number
- JPH042761A JPH042761A JP2101674A JP10167490A JPH042761A JP H042761 A JPH042761 A JP H042761A JP 2101674 A JP2101674 A JP 2101674A JP 10167490 A JP10167490 A JP 10167490A JP H042761 A JPH042761 A JP H042761A
- Authority
- JP
- Japan
- Prior art keywords
- film
- wear
- base material
- pressure
- composite material
- 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
Landscapes
- Physical Vapour Deposition (AREA)
- Coating By Spraying Or Casting (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、耐摩耗性及び熱間硬さに優れた高速度鋼とF
e基基材材の組み合わせにより、高厚膜及び高緻密性を
有する耐摩耗性複合材料及びその製造方法に関する。Detailed Description of the Invention [Industrial Field of Application]
The present invention relates to a wear-resistant composite material that has a high thickness and high density by combining e-base materials, and a method for producing the same.
[従来の技術]
基材に耐摩耗性材料を被覆することによる耐摩耗性複合
材料の従来の製造法には次のようなものがある。[Prior Art] Conventional methods for producing wear-resistant composite materials by coating a base material with wear-resistant materials include the following.
(1)カプセルHIP法
これは、第7図に示すように基材1の周囲をその形状に
合わせたカプセル2で囲み、カプセル2と基材1との空
間に所要の耐摩耗性粉末合金3を充填し、脱気及びシー
ルを行ったのち、熱間静水圧処理(以下、HIP処理と
呼ぶ)を行って粉末合金3を焼結させ被覆する方法であ
る。(1) Capsule HIP method As shown in FIG. 7, in this method, a base material 1 is surrounded by a capsule 2 that matches the shape of the base material 1, and the required wear-resistant powder alloy 3 is placed in the space between the capsule 2 and the base material 1. In this method, the powder alloy 3 is filled, degassed and sealed, and then subjected to hot isostatic pressure treatment (hereinafter referred to as HIP treatment) to sinter and coat the powder alloy 3.
しかし、この方法はある程度厚膜化は可能であるが、曲
面等を有する複雑な形状品ではカプセル加工費が高くつ
くという問題がある。However, although this method allows the film to be thickened to some extent, there is a problem in that the capsule processing cost is high for products with complex shapes such as curved surfaces.
(2)溶射法
これは、プラズマ溶射法で耐摩耗性合金を被覆する方法
であり、複雑な形状品には特に適した方法であるが、皮
膜層の気孔の存在は避けられず緻密性が欠如する。また
、基材界面との接合力が弱いことも問題である。(2) Thermal spraying method This method uses plasma spraying to coat wear-resistant alloys, and is particularly suitable for products with complex shapes, but the presence of pores in the coating layer is unavoidable and the coating layer is dense. be lacking. Another problem is that the bonding force with the base material interface is weak.
(3)溶射後HIF処理する方法
上記(2)で溶射後にHIP処理をすれば皮膜の品質を
改善することが可能である。(3) Method of performing HIF treatment after thermal spraying If HIP treatment is performed after thermal spraying in the above (2), it is possible to improve the quality of the coating.
しかし、従来の溶射法では上記問題のために皮膜を厚く
することができず、一般に0.5〜1.5關の厚さで、
これ以上の厚膜化は困難であった。However, with the conventional thermal spraying method, it is not possible to thicken the coating due to the above problems, and the coating is generally 0.5 to 1.5 degrees thick.
It was difficult to make the film thicker than this.
(4)特公昭58−39228号の方法これは、Fe基
基材材W、Mo 、Co 、N1基合金、wc、vcを
含む自溶性合金等の耐熱耐摩耗性合金の粉末を溶射し、
その後HIP処理を加えた被覆方法で、上記(3)に属
する方法である。(4) Method of Japanese Patent Publication No. 58-39228 This method involves thermally spraying powder of heat-resistant and wear-resistant alloys such as Fe-based base materials W, Mo, Co, N1-based alloys, and self-fluxing alloys containing WC and VC.
This is a coating method that includes subsequent HIP treatment, and is a method that belongs to (3) above.
しかし、この方法でも厚膜化は対象となっておらず、ま
た溶射材料に高速度鋼を含んでいない。さらに溶射法と
してガス溶射法、プラズマ溶射法を示しているが、この
プラズマ溶射法は常圧下で行うものと解され、低圧プラ
ズマ溶射法の適用を示唆する記述は認められない。However, even with this method, thickening of the film is not targeted, and high-speed steel is not included in the thermal spray material. Furthermore, gas spraying and plasma spraying are shown as thermal spraying methods, but this plasma spraying method is understood to be performed under normal pressure, and there is no description suggesting the application of low-pressure plasma spraying.
[発明が解決しようとする課題]
上述の従来法に共通の問題は、皮膜層を大にできないこ
とである。仮にそれが可能であるとしても(例えば上記
(1)のカプセルHIP法)、緻密性・接合力の欠如等
が問題となって実質的に不可能である。[Problems to be Solved by the Invention] A problem common to the above-mentioned conventional methods is that the film layer cannot be made large. Even if this were possible (for example, the capsule HIP method described in (1) above), it would be practically impossible due to problems such as lack of compactness and bonding strength.
溶射法において厚膜化が不可能な理由としては、溶射粒
子の急冷により発生する内部応力(これは、冷却時の熱
収縮と相変態による体積変化に起因するものである)が
膜厚とともに増加し、剥離、割れを招く力として作用す
ること、皮膜内部の気孔、酸化物が割れへの抵抗を弱め
ること、皮膜と基材間の密着力の不足が剥離への抵抗を
弱めることなどがあげられる。The reason why it is impossible to thicken the film using thermal spraying is that the internal stress generated by the rapid cooling of the sprayed particles (this is due to volume change due to thermal contraction and phase transformation during cooling) increases with the film thickness. However, the pores and oxides inside the film weaken the resistance to cracking, and the lack of adhesion between the film and the base material weakens the resistance to peeling. It will be done.
一方、高厚膜化が可能になれば、特に複雑な形状品、例
えば棒鋼、線材の製造ラインに使用されるガイドロール
等に適用でき、しかも摩耗の程度に応じて皮膜層を研削
することにより何回でも再使用可能となるので、耐用性
、コスト面でのメリットは大きい。On the other hand, if it becomes possible to increase the thickness of the film, it can be applied to products with particularly complex shapes, such as guide rolls used in production lines for steel bars and wire rods. Since it can be reused any number of times, it has great advantages in terms of durability and cost.
そこで、本発明者らは高膜厚を得る目的で、まず皮膜材
料の選定にあたり、耐摩耗性及び熱間硬さに優れた高速
度鋼を中心に各種の試験を行い、その結果、特定の製造
プロセスの下では十分目的を達成し得ることを確認した
。Therefore, in order to obtain a high film thickness, the present inventors first conducted various tests on high-speed steel, which has excellent wear resistance and hot hardness, in selecting a film material. It was confirmed that the manufacturing process was sufficient to achieve the purpose.
したがって、本発明の目的は、上記の知見に基づき、高
膜厚を持つ安価で耐摩耗性に富む複合材料及びその製造
方法を提供することにある。Therefore, an object of the present invention is to provide a composite material having a high film thickness, which is inexpensive and highly wear resistant, and a method for manufacturing the same, based on the above findings.
[課題を解決するための手段]
上記の目的を達成する本発明に係る耐摩耗性複合材料は
、Fe基の基材と、その上に被覆された高速度鋼を主成
分とする厚さ3 mm以上の溶射皮膜との組み合わせか
ら成るものである。[Means for Solving the Problems] A wear-resistant composite material according to the present invention that achieves the above object has a thickness of 3. It consists of a combination with a thermal spray coating of mm or more.
溶射材料の高速度鋼は、耐摩耗性及び熱間硬さに優れた
ものとして知られているW系、Mo系、V系のいずれで
もよいが、中でも高V系のものが適当である。The high-speed steel used as the thermal spraying material may be W-based, Mo-based, or V-based, which are known to have excellent wear resistance and hot hardness, but among them, high-V steel is suitable.
この耐摩耗性複合材料を製造するには、まず基材を60
0℃以上に予熱し、次いてこの予熱温度下にある基材の
表面に低圧プラズマ溶射法を適用して上記の高速度鋼を
主成分とする溶射材料を溶射し皮膜を形成する。To manufacture this wear-resistant composite material, the base material is first
The base material is preheated to 0° C. or higher, and then a low-pressure plasma spraying method is applied to the surface of the base material under this preheating temperature to spray the above-mentioned high-speed steel-based thermal spray material to form a coating.
この場合のプラズマ溶射は、酸素分圧が2Torr以下
で、全圧が20〜300 Torrの減圧雰囲気の条件
下で行うものとする。The plasma spraying in this case is performed under a reduced pressure atmosphere with an oxygen partial pressure of 2 Torr or less and a total pressure of 20 to 300 Torr.
その後、皮膜層の緻密化のためHIP処理を行う。Thereafter, HIP treatment is performed to densify the film layer.
また、上記HIP処理に代えて皮膜層の焼入れ焼戻しを
行ってもよい。さらにこのHIP処理と熱処理の双方を
行ってもよい。Furthermore, instead of the above-mentioned HIP treatment, the coating layer may be quenched and tempered. Furthermore, both this HIP treatment and heat treatment may be performed.
[作 用]
まず、複合材料の組み合わせを、Fe基の基材と高速度
鋼の被覆材料とすることで、高速度鋼の持つ耐摩耗性及
び熱間硬さの特長を十分に発揮させることできる。また
両材料は熱膨張率が接近しているため(例えば、炭素鋼
の線膨張率11X10−6/”C,高速度鋼の線膨張率
11×10−6/℃)、溶射終了後、予熱温度から室温
までの冷却時における熱応力を抑止でき、皮膜と基材間
の密着力が高い。[Function] First, by combining the composite materials with a Fe-based base material and a coating material of high-speed steel, the features of high-speed steel, such as wear resistance and hot hardness, can be fully demonstrated. can. In addition, since the coefficients of thermal expansion of both materials are close to each other (for example, the coefficient of linear expansion of carbon steel is 11×10-6/"C, and the coefficient of linear expansion of high-speed steel is 11×10-6/"C), preheating is required after thermal spraying. It can suppress thermal stress during cooling from temperature to room temperature, and has high adhesion between the film and the base material.
次に、溶射前に基材を600℃以上に予熱しておくこと
により、溶射粒子の急冷を防止できるため溶射粒子間の
熱歪に基づく内部応力が低減し、また溶射期間中溶射粒
子の熱活性化が保たれるため内部応力が緩和する。その
結果、厚膜としても皮膜の剥離、割れ等を生じにくいの
である。Next, by preheating the base material to 600°C or higher before thermal spraying, it is possible to prevent the thermal spray particles from rapidly cooling, which reduces internal stress due to thermal distortion between the thermal spray particles, and also to reduce the internal stress caused by thermal distortion between the thermal spray particles. Since activation is maintained, internal stress is relaxed. As a result, even if the film is thick, peeling or cracking of the film is less likely to occur.
第3図は酸素分圧、雰囲気全圧が上記の規定値以内で3
mm以上の膜厚を得るには、最小限基材予熱温度をい
くらにしたらよいかを調べた線図であり、基材予熱温度
(”C)の変化により、剥離を生ずることなく形成可能
な最大膜厚(w )を表している。第3図から、膜厚3
mm以上を得るには、基材予熱温度を600℃以上に保
持すべきことがわかる。Figure 3 shows that the oxygen partial pressure and total atmospheric pressure are within the specified values above.
This is a diagram that examines the minimum substrate preheating temperature that should be used to obtain a film thickness of mm or more, and it is possible to form a film without peeling by changing the substrate preheating temperature ("C). It represents the maximum film thickness (w).From Figure 3, film thickness 3
It can be seen that in order to obtain a temperature of 600° C. or higher, the base material preheating temperature should be maintained at 600° C. or higher.
次に、上記の予熱温度条件下で、基材表面に、JIS
G 4403相当の高速度鋼粉末を酸素分圧2 Tor
r以下、全圧20〜300 Torrの減圧雰囲気下で
プラズマ溶射し皮膜を形成する。Next, under the above preheating temperature conditions, JIS
High speed steel powder equivalent to G 4403 was heated to an oxygen partial pressure of 2 Torr.
A film is formed by plasma spraying under a reduced pressure atmosphere with a total pressure of 20 to 300 Torr.
まず、酸素分圧を低く限定することで、予熱中の基材及
び溶射粒子の酸化が防止される。そのため、皮膜の割れ
の原因となる酸化物が減少する。First, by limiting the oxygen partial pressure to a low level, oxidation of the substrate and thermal spray particles during preheating is prevented. Therefore, oxides that cause cracks in the film are reduced.
第1図は酸素分圧(Torr)の影響を抗折力()cg
/關2)の変化で調べた線図であり、この図から、酸素
分圧が低いほど抗折力は安定しており、酸素分圧が2
Torrを越えると、抗折力ひいては皮膜の割れの抵抗
力が急激に低下することがゎがる。Figure 1 shows the effect of oxygen partial pressure (Torr) on transverse rupture force ()cg
This is a diagram examined based on the change in 2). From this diagram, it can be seen that the lower the oxygen partial pressure, the more stable the transverse rupture force is, and the lower the oxygen partial pressure is
When Torr is exceeded, the transverse rupture strength and, in turn, the resistance to cracking of the coating are likely to decrease rapidly.
次に、雰囲気全圧を上記の低圧条件とすることで、溶射
粒子の加熱溶融を促進し、粒子飛行速度を増大させるた
め、皮膜中の気孔が減り、緻密性が向上し、この結果耐
摩耗性が向上する。また気孔中のガス圧が低いため、後
工程のHIP処理にも都合がよい。Next, by setting the total atmospheric pressure to the above-mentioned low pressure condition, the heating and melting of the sprayed particles is promoted and the particle flight speed is increased, so the pores in the film are reduced and the density is improved, resulting in wear resistance. Improves sex. Furthermore, since the gas pressure in the pores is low, it is convenient for the HIP treatment in the post-process.
第2図は酸素分圧が2Torrのもとで、雰囲気全圧(
Torr)の影響を皮膜の気孔体積率(%)の変化で調
べた線図であり、雰囲気全圧が300 Torr以下で
あれば、気孔はほとんど生じない。なお、全圧の下限値
は実用的経済性の見地から定めている。Figure 2 shows the total atmospheric pressure (
This is a diagram in which the influence of pore volume (%) in the film was examined by changing the pore volume ratio (%) of the film.If the total atmospheric pressure is 300 Torr or less, almost no pores are formed. Note that the lower limit value of the total pressure is determined from the viewpoint of practical economy.
そして最後に、皮膜中にわずかに残る気孔を消失させ完
全に緻密化するために、HIP処理を行う。なお、HI
P条件は、1100℃X 1500kg / cd X
1時間としている。Finally, HIP treatment is performed to eliminate the few remaining pores in the film and completely densify it. In addition, HI
P conditions are 1100℃ x 1500kg/cd
It is set as 1 hour.
このHIP処理に代えて焼入れ焼戻しを行っても同等程
度の緻密性が得られる。また、HIP処理後に焼入れ焼
戻しを行ってもよいことはいうまでもない。Even if quenching and tempering is performed instead of this HIP treatment, the same level of density can be obtained. Furthermore, it goes without saying that quenching and tempering may be performed after the HIP treatment.
熱処理後の皮膜組織の顕微鏡写真を第4図(a)に示す
。また、比較のため従来のカプセルHIP法で処理した
ままの皮膜組織の顕微鏡写真を第4図(b)に示す。な
お、基材材質及び被覆材料は両者共同じである。A microscopic photograph of the film structure after heat treatment is shown in FIG. 4(a). For comparison, FIG. 4(b) shows a microscopic photograph of the film structure as it was treated by the conventional capsule HIP method. Note that the base material and coating material are the same for both.
両者を対比すれば、明らかに本発明の皮膜組織は緻密化
が著しく進行しており、かつ、w、v等の炭化物は5μ
m以下に微細化され、均一に分散していることがわかる
。Comparing the two, it is clear that the film structure of the present invention has been significantly densified, and the carbides such as w and v are 5μ
It can be seen that the particles are finely divided to less than m and are uniformly dispersed.
[実施例]
本発明において、基材予熱温度、酸素分圧、及び雰囲気
全圧の影響を調べるために、次のような試験を行った。[Example] In the present invention, the following tests were conducted in order to investigate the effects of substrate preheating temperature, oxygen partial pressure, and total atmosphere pressure.
試験は三段階に分けて実施した。The test was conducted in three stages.
試験1:最初に、気孔の無い緻密な皮膜を形成し、その
上で酸化物巻き込みの観点がら、抗折力の低下しない溶
射雰囲気中の酸素分圧の上限を調べた。Test 1: First, a dense film without pores was formed, and then, from the viewpoint of oxide inclusion, the upper limit of the oxygen partial pressure in the spraying atmosphere without reducing the transverse rupture strength was investigated.
試験2:次に、気孔の存在が耐摩耗性を低下させるため
、溶射に引き続<I(IP処理によって、完全に気孔の
無くなる溶射雰囲気の全圧の上限を調べた。Test 2: Next, since the presence of pores reduces wear resistance, the upper limit of the total pressure of the thermal spraying atmosphere that completely eliminates pores was investigated by <I (IP treatment) following thermal spraying.
試験3:最後に、上記二条性を満たした上で、3龍以上
の膜厚が形成できる基材の予熱温度を調べた。Test 3: Finally, the preheating temperature of the base material at which a film thickness of 3 dragons or more could be formed while satisfying the above-mentioned double-stripe property was investigated.
試験条件及び結果
共通条件
被覆材料
5KHIO相当組成の合金粉末
粒径100μm以下
低圧プラズマ溶射機
Ar−20%H2
溶射機
プラズマガス
溶射電流
基材材質
基材寸法
00 A
45C
直径80mra、高さ100m+*の円柱体(第5図参
照、図中、1は
基材、4は皮膜である)
試験1
基材予熱温度 800℃
雰囲気全圧 100 Torr
被覆厚 5 mm
溶射後HIP条件 1100℃X 1500kg /
cd X I Hr熱処理 焼入れ1230
℃X 1.5 win加熱後油冷
焼戻し 550℃X8Hr
加熱後空冷
試験方法と結果
皮膜4より、直径5 mmの丸棒状試験片を採取し、3
点曲げ試験機にて抗折力を求めた。Test conditions and results Common conditions Coating material 5KHIO equivalent composition alloy powder Particle size 100μm or less Low pressure plasma spraying machine Ar-20%H2 Thermal spraying machine Plasma gas spraying Current Base material Base material dimensions 00 A 45C Diameter 80 mra, height 100 m + * Cylindrical body (see Figure 5, 1 is the base material and 4 is the coating) Test 1 Base material preheating temperature 800°C Total atmosphere pressure 100 Torr Coating thickness 5 mm HIP conditions after thermal spraying 1100°C x 1500 kg /
cd X I Hr heat treatment quenching 1230
℃X 1.5win Heating then oil cooling tempering 550℃X8Hr Heating then air cooling Test method and results From film 4, a round rod-shaped test piece with a diameter of 5 mm was taken.
Transverse rupture strength was determined using a point bending tester.
その結果を第1図に示す。The results are shown in FIG.
これより、皮膜品質の点からは、酸素分圧を2Torr
以下にしなければならないことが明らかとなった。From this, from the point of view of film quality, the oxygen partial pressure should be set at 2 Torr.
It became clear that the following had to be done.
試験2
基材予熱温度 800℃
酸素分圧 2 Torr
被覆厚 3mm
溶射後HIP条件 1100℃X 1500kg /
cd X I Hr試験方法と結果
皮膜4より試験片を採取し、光学顕微鏡観察により、気
孔の体積率を求めた。Test 2 Base material preheating temperature 800℃ Oxygen partial pressure 2 Torr Coating thickness 3mm HIP conditions after thermal spraying 1100℃X 1500kg /
cd
その結果を第2図に示す。The results are shown in FIG.
これより、HIP後において、完全に気孔の無い緻密な
膜を得るには溶射時の雰囲気の全圧を300Torr以
下にしなければならないことが明らかとなった。From this, it has become clear that in order to obtain a dense film completely free of pores after HIP, the total pressure of the atmosphere during thermal spraying must be 300 Torr or less.
試験3
雰囲気全圧 100 Torr
酸素分圧 2 Torr
試験方法と結果
溶射後室温まで試験体を冷却したときの、皮膜の剥離を
生じない最大の膜厚を求めた。Test 3 Atmospheric total pressure: 100 Torr Oxygen partial pressure: 2 Torr Test method and results When the test specimen was cooled to room temperature after thermal spraying, the maximum film thickness without peeling of the film was determined.
その結果を第3図に示す。The results are shown in FIG.
これより、試験1,2で求めた、良好な品質を有する皮
膜形成条件下において、3mm以上の厚い皮膜を得るに
は600℃以上の基材予熱温度の必要なことか明らかと
なった。From this, it became clear that under the conditions for forming a film with good quality as determined in Tests 1 and 2, it is necessary to preheat the substrate at a temperature of 600° C. or higher in order to obtain a thick film of 3 mm or more.
実施例
以下の基本条件を使用し、本発明に関わる条件を変化さ
せた試験を実施した。EXAMPLES Tests were conducted using the basic conditions described below and varying the conditions related to the present invention.
試験条件と試験結果は第1表のとおりである。The test conditions and test results are shown in Table 1.
最初に、皮膜に剥離、割れ等を生じない膜厚を決定した
。本発明の目的は311℃m以上の皮膜の得られる条件
である。First, we determined the film thickness that would not cause peeling or cracking of the film. The object of the present invention is to provide conditions under which a film having a temperature of 311° C.m or higher can be obtained.
次に、割れ、剥離のない皮膜の得られる範囲内の膜厚に
おいて試験材を作製し、HIF処理の後、各種試験片を
採取して性能を調べた。Next, test materials were prepared with a film thickness within a range that provided a film without cracking or peeling, and after HIF treatment, various test pieces were taken to examine performance.
皮膜の密度は、HIP処理後のサンプルについて、顕微
鏡で空孔の体積率を調べ、空孔の無い完全緻密な状態を
100%の密度とした。The density of the film was determined by examining the volume ratio of pores under a microscope for the sample after HIP treatment, and a completely dense state with no pores was defined as 100% density.
抗折力試験及び摩耗試験に当たっては、高速度鋼被覆材
は焼入れ焼戻しを行った後に試験に供した。In the transverse rupture strength test and the wear test, the high-speed steel coating material was subjected to quenching and tempering before being subjected to the test.
耐摩耗性はアムスラー式摩耗試験機により評価した。こ
の試験法は、第6図に示すように345C製の直径40
mm、厚さ3 mmの回転円盤5の外周面に、水金しな
がら試験片6を50kgの力で押し当てて、摩擦距離5
00m摺動させた後、試験片6の摩耗幅を測定すること
により実施した。Abrasion resistance was evaluated using an Amsler abrasion tester. This test method uses 345C diameter 40mm as shown in Figure 6.
A test piece 6 was pressed against the outer peripheral surface of a rotating disk 5 with a thickness of 3 mm with a force of 50 kg while water was being applied, and a friction distance of 5
The test was carried out by measuring the wear width of the test piece 6 after sliding it for 00 m.
試験条件
基材材質
基材寸法
被覆材料
45C
直径80mm、高さ10011I+1の円柱体(第5図
参照)
A:5KH10相当組成粉末
粒径100μm以下
B:超硬粉末(VC−17%Co)
粒径100μm以下
溶射条件
溶射法 プラズマ溶射法
試験片No、 1〜7−低圧プラズマ溶射性試験片No
、8 −常圧プラズマ溶射法プラズマガス Ar−2
0%H2
電流 800 A
溶射後HIP条件 1100℃X 1500kg /
cd X I Hr被覆後熱処理
焼入れ1230℃x 1,5 sin
加熱後油冷
550℃X’lHr
加熱後空冷炉冷
焼戻し
第1表から、本発明の条件を満たすもの(試験No、1
〜3)は、膜厚、抗折力、密度、及び耐摩耗性の全ての
面で優れていることがわかる。Test conditions Base material Base material Dimensions Covering material 45C Cylindrical body with diameter 80 mm and height 10011I+1 (see Figure 5) A: 5KH10 equivalent composition Powder particle size 100 μm or less B: Carbide powder (VC-17%Co) Particle size 100 μm or less Thermal spraying conditions Plasma spraying test piece No. 1 to 7-Low pressure plasma spraying test piece No.
, 8 - Normal pressure plasma spraying plasma gas Ar-2
0%H2 Current 800 A HIP conditions after thermal spraying 1100℃X 1500kg /
cd
It can be seen that samples 3) to 3) are excellent in all aspects of film thickness, transverse rupture strength, density, and abrasion resistance.
また、高膜厚を得られるとしても、基材予熱温度、酸素
分圧、雰囲気全圧が皮膜の品質上重要であることか、試
験Nα4.5.6からもわかる。Furthermore, even if a high film thickness can be obtained, test Nα4.5.6 shows that the substrate preheating temperature, oxygen partial pressure, and total atmosphere pressure are important for the quality of the film.
そして、比較材として示した試験NG、 7 、8では
、皮膜の割れ、剥離を生じ、使用不能である。特に、常
圧プラズマ溶射法(試験No、8)では被覆ができない
。In Tests NG, 7, and 8 shown as comparative materials, cracking and peeling of the film occurred, making them unusable. In particular, the normal pressure plasma spraying method (Test No. 8) cannot provide a coating.
[発明の効果コ
以上のように本発明によれば、耐摩耗性、耐用性に優れ
た安価な複合材料の提供が可能となる。[Effects of the Invention] As described above, according to the present invention, it is possible to provide an inexpensive composite material with excellent wear resistance and durability.
また、皮膜の高厚膜化、高緻密化が可能である。Furthermore, it is possible to make the film thicker and more dense.
第1図は本発明において低圧プラズマ溶射法の適用に際
し、酸素分圧の影響を抗折力の面から調べた線図、第2
図は同じく雰囲気全圧の影響を気孔体積率の面から調べ
た線図、第3図は同じく基材予熱温度の影響を最大膜厚
の面から調べた線図、第4図(a)、(b)は本発明及
び従来の場合を比較して示す皮膜組織写真、第5図は本
発明の実施例に供した試験体の斜視図、第6図は摩耗試
験方法の説明図、第7図は従来のカプセルHIP法の説
明図である。
1・・・基材
4・・・皮膜
代理人 弁理士 佐々木 宗 治Figure 1 is a diagram examining the influence of oxygen partial pressure from the perspective of transverse rupture strength when applying the low-pressure plasma spraying method in the present invention;
The figure is a diagram similarly examining the influence of the total atmospheric pressure from the perspective of pore volume fraction, Figure 3 is a diagram similarly examining the influence of substrate preheating temperature from the aspect of maximum film thickness, and Figure 4 (a). (b) is a photograph of the film structure comparing the present invention and the conventional case, FIG. The figure is an explanatory diagram of the conventional capsule HIP method. 1... Base material 4... Film agent Patent attorney Muneharu Sasaki
Claims (4)
鋼を主成分とする厚さ3mm以上の溶射皮膜とを有する
耐摩耗性複合材料。(1) A wear-resistant composite material comprising an Fe-based base material and a thermal sprayed coating with a thickness of 3 mm or more, the main component of which is high-speed steel, applied to the surface of the base material.
、前記基材の表面に高速度鋼を主成分とする材料を酸素
分圧が2Torr以下、全圧が20〜300Torrの
減圧雰囲気下でプラズマ溶射して皮膜を形成し、その後
熱間静水圧処理を行うことを特徴とする耐摩耗性複合材
料の製造方法。(2) A Fe-based base material is heated to 600°C or higher in advance, and a material mainly composed of high-speed steel is applied to the surface of the base material under a reduced pressure atmosphere with an oxygen partial pressure of 2 Torr or less and a total pressure of 20 to 300 Torr. A method for manufacturing a wear-resistant composite material, which comprises forming a film by plasma spraying and then subjecting it to hot isostatic pressure treatment.
うことを特徴とする請求項2記載の耐摩耗性複合材料の
製造方法。(3) The method for manufacturing a wear-resistant composite material according to claim 2, wherein a heat treatment of quenching and tempering is performed after the plasma spraying.
行うことを特徴とする請求項2記載の耐摩耗性複合材料
の製造方法。(4) The method for manufacturing a wear-resistant composite material according to claim 2, characterized in that a heat treatment of quenching and tempering is performed after the hot isostatic pressure treatment.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2101674A JPH0794705B2 (en) | 1990-04-19 | 1990-04-19 | Abrasion resistant composite material and manufacturing method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2101674A JPH0794705B2 (en) | 1990-04-19 | 1990-04-19 | Abrasion resistant composite material and manufacturing method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH042761A true JPH042761A (en) | 1992-01-07 |
| JPH0794705B2 JPH0794705B2 (en) | 1995-10-11 |
Family
ID=14306909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2101674A Expired - Fee Related JPH0794705B2 (en) | 1990-04-19 | 1990-04-19 | Abrasion resistant composite material and manufacturing method thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0794705B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006312767A (en) * | 2005-05-09 | 2006-11-16 | Ayabo:Kk | Surface treatment method for imparting abrasion resistance and oxidation resistance to steel member |
| WO2015045038A1 (en) * | 2013-09-25 | 2015-04-02 | 中国電力株式会社 | Method for diffusion coating heat-resistant metal member with creep reinforcement material, and creep-strength-enhanced heat-resistant metal member |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0288756A (en) * | 1988-09-22 | 1990-03-28 | Kubota Ltd | Method of forming wear-resistant coating |
| JPH02101675A (en) * | 1988-10-06 | 1990-04-13 | Canon Inc | optical information processing device |
| JPH02101677A (en) * | 1988-10-07 | 1990-04-13 | Sharp Corp | Recording and reproducing method |
-
1990
- 1990-04-19 JP JP2101674A patent/JPH0794705B2/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0288756A (en) * | 1988-09-22 | 1990-03-28 | Kubota Ltd | Method of forming wear-resistant coating |
| JPH02101675A (en) * | 1988-10-06 | 1990-04-13 | Canon Inc | optical information processing device |
| JPH02101677A (en) * | 1988-10-07 | 1990-04-13 | Sharp Corp | Recording and reproducing method |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006312767A (en) * | 2005-05-09 | 2006-11-16 | Ayabo:Kk | Surface treatment method for imparting abrasion resistance and oxidation resistance to steel member |
| WO2015045038A1 (en) * | 2013-09-25 | 2015-04-02 | 中国電力株式会社 | Method for diffusion coating heat-resistant metal member with creep reinforcement material, and creep-strength-enhanced heat-resistant metal member |
| CN105555988A (en) * | 2013-09-25 | 2016-05-04 | 中国电力株式会社 | Method for diffusion coating heat-resistant metal member with creep reinforcement material, and creep-strength-enhanced heat-resistant metal member |
| JPWO2015045038A1 (en) * | 2013-09-25 | 2017-03-02 | 中国電力株式会社 | Diffusion / penetration method of creep reinforcement for heat-resistant metal material member and method for producing heat-resistant metal material member with enhanced creep strength |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0794705B2 (en) | 1995-10-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7840935B2 (en) | Method for manufacturing hot rolling rolls by laser cladding | |
| CN115703153B (en) | A method for optimizing nickel-titanium alloy performance based on laser selective melting | |
| CN110066995A (en) | A kind of cladding alloy powder and the laser cladding method for carrying out H13 mould steel | |
| CN114411067B (en) | Medium-carbon hot work die steel material and additive manufacturing method based on same | |
| GB2095291A (en) | Fabrication of gas turbine nozzles | |
| JPH02290951A (en) | Wear resistant composite roll and its production | |
| US4562090A (en) | Method for improving the density, strength and bonding of coatings | |
| GB2262540A (en) | Enhancement of hot workability of titanium alloy by coating with titanium | |
| JP4731645B2 (en) | Cemented carbide and coated cemented carbide and method for producing the same | |
| JP3522590B2 (en) | High hardness carbide cermet thermal spray coating member and method of manufacturing the same | |
| JPH042761A (en) | Wear-resistant composite material and its manufacturing method | |
| EP0605175B1 (en) | A coated article and a method of coating said article | |
| CN116949381A (en) | Preparation method of ultra-high-speed laser cladding high-hardness high-wear-resistance coating | |
| JPH03193204A (en) | Plug for manufacturing hot seamless tube | |
| JPH042762A (en) | Abrasion resistant roll and its manufacturing method | |
| US4306907A (en) | Age hardened beryllium alloy and cermets | |
| JPH042763A (en) | Production of wear resistant alloy | |
| JPH0288756A (en) | Method of forming wear-resistant coating | |
| CN114833342B (en) | Powder metallurgy wear-resistant high-toughness die steel and processing technology thereof | |
| JPH02221373A (en) | Coated cemented carbide for wear resistant tool and production thereof | |
| JPH03193848A (en) | Wear resistant roll and its production | |
| SU893371A2 (en) | Method of producing articles from hard-to-machine materials | |
| JPH02294457A (en) | Thick film coating method for metal substrates | |
| Lopata et al. | Research into the possibility of improving the quality of electric arc coatings by nitriding | |
| JPH08246123A (en) | Carbon member having a metal compound coating layer having excellent adhesion durability and method for producing the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |