JPS6237356A - Manufacture of co base alloy member superior in wear resistance - Google Patents

Manufacture of co base alloy member superior in wear resistance

Info

Publication number
JPS6237356A
JPS6237356A JP17475085A JP17475085A JPS6237356A JP S6237356 A JPS6237356 A JP S6237356A JP 17475085 A JP17475085 A JP 17475085A JP 17475085 A JP17475085 A JP 17475085A JP S6237356 A JPS6237356 A JP S6237356A
Authority
JP
Japan
Prior art keywords
dispersed
carbides
wear resistance
alloy member
secondary carbides
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
Application number
JP17475085A
Other languages
Japanese (ja)
Other versions
JPS634906B2 (en
Inventor
Nobuyoshi Kurauchi
倉内 伸好
Masaaki Kato
公明 加藤
Katsuhisa Kawakami
川上 勝久
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Metal Corp
Original Assignee
Mitsubishi Metal Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Metal Corp filed Critical Mitsubishi Metal Corp
Priority to JP17475085A priority Critical patent/JPS6237356A/en
Publication of JPS6237356A publication Critical patent/JPS6237356A/en
Publication of JPS634906B2 publication Critical patent/JPS634906B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Heat Treatment Of Steel (AREA)
  • Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)

Abstract

PURPOSE:To manufacture the titled member, by soln. heat treating Co base alloy member contg. specified compsn. quantities of C, W, Mo, Cr, then providing surface strain by shot blasting, and applying a suitable aging treatment thereto. CONSTITUTION:Co base alloy member having a compsn. composed of, by weight 0.05-2% C, 2-20% one or more kinds of W or Mo, 15-35% Cr further if necessary 1-25% of one or more kinds of Ni or Fe and the balance Co with inevitable impurities is soln. heat treated under conventional condition. Next, the number is shot blasted to provide surface strain, successively aging treated at 700-1,000 deg.C. In this way, the structure of at least surface part is made to that in which primary and secondary carbides are dispersed in matrix and grain boundary respectively, further fine secondary carbides having <=1mum diameter are dispersed in grain, hardness is improved and wear resistance is remarkably improved.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発゛明は、すぐれた耐摩耗性を有し、かつ耐熱性に
もすぐれたCo基合金部材の製造法に関するものである
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for producing a Co-based alloy member having excellent wear resistance and heat resistance.

〔従来の技術〕[Conventional technology]

一般、に、チェンソーガイドや、木工加工用並びに軽金
属および合金切断用のこ歯、さらに蒸気タービンのブレ
ード、各種のシャフト部品やバルブ部品などの製造には
、すぐれた耐摩耗性と耐熱性が要求されることから、各
種のCo基合金が用いられている。
In general, excellent wear resistance and heat resistance are required for manufacturing chain saw guides, saw teeth for woodworking, light metal and alloy cutting, steam turbine blades, various shaft parts, valve parts, etc. Therefore, various Co-based alloys are used.

また、これらの各種Co基合金のうちの1つとして1重
量%で(以下チは重量%を示す)。
Also, one of these various Co-based alloys is 1% by weight (hereinafter, ``chi'' indicates % by weight).

C:0.05〜2%。C: 0.05-2%.

WおよびMoのうちの1種または2種:2〜20%1 Cr:15〜35%、 を含有し、さらに必要に応じて。One or two of W and Mo: 2-20%1 Cr: 15-35%, Contains and further if necessary.

N1およびFeのうちの1種または2種:1〜25チ。One or two of N1 and Fe: 1 to 25 chi.

を含有し、残りがCOと不可避不純物からなる組成を有
するCo基合金が広く知られている。
Co-based alloys are widely known which have a composition containing CO and the remainder consisting of CO and unavoidable impurities.

これらのCo基合金部材は1例えば板材である場合1通
常、鋳造後のインゴットに1分塊鍛造や分塊圧延、さら
に熱間圧延や冷間圧延を施して、板厚:約1〜4Bを有
する板材とし、これに1100〜1250℃の温度で溶
体化処理を施すことによって製造され、この状態で実用
に供されている。
For example, when these Co-based alloy members are plate materials, 1 the ingot after casting is usually subjected to 1-blunt forging, blooming rolling, and further hot rolling or cold rolling to obtain a plate thickness of approximately 1 to 4 B. It is manufactured by subjecting this plate material to solution treatment at a temperature of 1100 to 1250°C, and is put into practical use in this state.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかし、近年、上記の利用分野においても高速′化や高
性能化が要求されるようになっており、これに伴って、
上記の従来Co基合金部材のもつ耐摩耗性のより一層の
向上が望まれている。
However, in recent years, there has been a demand for higher speed and higher performance in the above application fields, and with this,
It is desired to further improve the wear resistance of the above-mentioned conventional Co-based alloy members.

〔問題点を解決するだめの手段〕[Failure to solve the problem]

そこで2本発明者等は、上述のような観点から、上記の
従来COi合金部材に着目し、これのもつ耐摩耗性を一
段と向上せしめるべく研究を行なった結果、上記従来C
o基合金部材は、溶体化処理後、素地に1次炭化物が分
散し、かつ2次炭化物が結晶粒界だけに析出した組織を
もつが、との溶体化処理後のCo基合金部材に、ショツ
トブラストによる表面歪を付与した後、700〜100
0℃の温度で時効処理を施すと、この結果のCo基合金
部材においては、1次炭化物が素地中に、また2次炭化
物が結晶粒界に分散した状態で存在するが、特に表面部
において2次炭化物が結晶粒内に析出した組織をもつよ
うになり、しかもこの結晶粒内に析出した2次炭化物は
直径:1μm以下の微細なものであるため1結晶粒内の
硬さが、従来Co基合金板材ではビッカース硬さで約2
50であったものが1同300程度にまで向上し、耐摩
耗性の著しい改善がはかれるようになるという知見を得
たのである。
Therefore, from the above-mentioned viewpoint, the present inventors focused on the above-mentioned conventional COi alloy member and conducted research to further improve the wear resistance of the above-mentioned conventional COi alloy member.
After solution treatment, the O-based alloy member has a structure in which primary carbides are dispersed in the matrix and secondary carbides are precipitated only at the grain boundaries. 700-100 after applying surface strain by shot blasting
When aging treatment is carried out at a temperature of 0°C, in the resulting Co-based alloy member, primary carbides exist in the matrix and secondary carbides are dispersed in the grain boundaries, but especially in the surface area. It now has a structure in which secondary carbides are precipitated within the crystal grains, and since the secondary carbides precipitated within the crystal grains are fine with a diameter of 1 μm or less, the hardness within one crystal grain is lower than that of the conventional one. Co-based alloy plate material has a Vickers hardness of approximately 2
They obtained the knowledge that the wear resistance was improved from 50 to about 300 per day, resulting in a significant improvement in wear resistance.

したがって、この発明は、上記知見にもとづいてなされ
たものであって。
Therefore, this invention has been made based on the above findings.

C:0.05〜2チ。C: 0.05 to 2 inches.

WおよびMoのうちの1種または2種:2〜20チ。One or two of W and Mo: 2 to 20.

Cr:15〜35%。Cr: 15-35%.

を含有し、さらに必要に応じて、 N1およびFeのうちの1種または2種=1〜25チ。Contains, and if necessary, One or two of N1 and Fe = 1 to 25.

を含有し、残シがCOと不可避不純物からなる組成を有
し、かつ通常の条件で溶体化処理を施したCo基合金部
材に、ショツトブラストによる表面歪を付与した状態で
、700〜1000℃の温度で時効処理を施すことによ
って、少なくとも表面部が、素地中に1次炭化物が、ま
た結晶粒界に2次炭化物が分散し、さらに結晶粒内に直
径:1μm以下の2次炭化物が分散した組織を有する。
A Co-based alloy member containing CO and unavoidable impurities as a residue and subjected to solution treatment under normal conditions was heated at 700 to 1000°C with surface strain imparted by shot blasting. By performing aging treatment at a temperature of , primary carbides are dispersed in the matrix, secondary carbides are dispersed in the grain boundaries, and secondary carbides with a diameter of 1 μm or less are further dispersed in the crystal grains, at least in the surface area. It has an organized structure.

耐摩耗性の著しくすぐれたCo基合金部材を製造する方
法に特徴を有するものである。
The present invention is characterized by a method for manufacturing a Co-based alloy member with extremely high wear resistance.

つぎに、この発明の方法において、 Co基合金部材の
成分組成および時効処理温度を上記の通りに限定した理
由を説明する。
Next, in the method of the present invention, the reason why the composition and aging treatment temperature of the Co-based alloy member are limited as described above will be explained.

A、成分組成 (a)  C C成分には、炭化物を形成して耐摩耗性を向上させる作
用があるが、その含有量が0.05%未満では、特に2
次炭化物の析出が不十分となり、所望の耐摩耗性を確保
することができず、一方その含有量が2チを越えると、
塑性加工が困難になることから、その含有量を0.05
〜2チと定めた。
A. Component composition (a) C The C component has the effect of forming carbide and improving wear resistance, but if its content is less than 0.05%, especially 2
Precipitation of secondary carbides becomes insufficient, making it impossible to secure the desired wear resistance.On the other hand, if the content exceeds 2.
Since plastic working becomes difficult, its content is reduced to 0.05.
It was set as ~2chi.

(b)  wおよびMo これらの成分には、一部が素地に固溶して、これを強化
するほか、炭化物を形成して耐摩耗性を向上させる作用
があるが、その含有量が2チ未満では前記作用に所望の
効果が得られず、一方その含有量が20%を越えると、
塑性加工性が低下するようになるほか、板材に脆化傾向
が現われるようになることから、その含有量を2〜20
%と定めた。
(b) w and Mo These components have the effect of forming a solid solution in the base material and strengthening it, as well as forming carbides and improving wear resistance. If the content is less than 20%, the desired effect cannot be obtained; on the other hand, if the content exceeds 20%,
In addition to decreasing plastic workability, the plate material also tends to become brittle, so the content should be reduced to 2 to 20%.
%.

(c)  Cr Cr成分には、素地に固溶して耐熱性を向上させるほか
、炭化物を形成して耐摩耗性を向上させる作用があるが
、その含有量が15%未満では前記作用に所望の効果が
得られず、一方その含有量が35%を越えると、σ相な
どの脆化相が出現するようになって塑性加工性および延
性が低下するようになることから、その含有量を15〜
35チと定めた。
(c) Cr The Cr component has the effect of improving heat resistance by forming a solid solution in the base material, as well as improving wear resistance by forming carbide, but if its content is less than 15%, the desired effect may not be achieved. On the other hand, if the content exceeds 35%, brittle phases such as σ phase will appear and plastic workability and ductility will decrease. 15~
It was set at 35chi.

(d)  NiおよびFe これらの成分には、素地に固溶して、延性および塑性加
工性を向上させる作用があるので、特にこれらの特性が
要求される場合に必要に応じて含有されるが、その含有
量が1チ未満では前記作用に所望の向上効果が得られず
、一方その含有量が25%を越えると耐摩耗性の低下が
著しくなることから、その含有量を1〜25%と定めた
(d) Ni and Fe These components dissolve in solid solution in the base material and have the effect of improving ductility and plastic workability, so they may be included as necessary when these properties are particularly required. If the content is less than 1 inch, the desired effect of improving the above action cannot be obtained, while if the content exceeds 25%, the wear resistance will be significantly lowered, so the content should be reduced from 1 to 25%. It was determined that

B9時効処処理炭 その温度が700℃未満では、特に表面歪を付与した表
面部における結晶粒内に微細な2次炭化物を十分析出さ
せることができず、一方その温度が1000℃を越える
と、1次および2次炭化物とも粗大化するようになって
所望の耐摩耗性を確保することができないことから、そ
の温度を700〜1000℃と定めた。
If the temperature of B9 aged treated coal is less than 700°C, fine secondary carbides cannot be produced sufficiently within the crystal grains, especially in the surface area where surface strain has been applied, while on the other hand, if the temperature exceeds 1000°C, Since both the primary and secondary carbides become coarse and the desired wear resistance cannot be ensured, the temperature is set at 700 to 1000°C.

実施例 つぎに、この発明の方法を実施例により具体的に説明す
る。
EXAMPLES Next, the method of the present invention will be specifically explained with examples.

通常の溶解法を用い、それぞれ第1表に示される成分組
成をもったCO基合金溶湯を調製し、鋳造して直径:9
0Bφ×長さ: 350ffjlの寸法をもったインゴ
ットとした後、このインゴットに、1200−4000
℃の温度での熱間鍛造、並びに1200〜1000℃で
の熱間圧延を施して板厚=211の熱延板とし、さらに
この熱延板に、  1200℃の温度に、0.5時間保
持後、空冷の条件で溶体化処理を施し、ついでこの溶体
化処理後の幅:100頗×厚さ:2鵡×長さ:200鵡
の寸法をもった板材に、ショツトブラスト機(直径:2
顛の鋼製ショット使用)を用い、それぞれ第1表に示さ
れる時間ショツトブラスト処理を行なって表面歪を付与
した後、大気中で、同じく第1表に示される温度で時効
処理(1時間保持後、空冷)を施すことによって本発明
法1〜22をそれぞれ実施した。
Molten CO-based alloys having the respective compositions shown in Table 1 were prepared using a normal melting method, and cast to diameter: 9.
0Bφ×Length: After making an ingot with dimensions of 350ffjl, this ingot was
A hot-rolled plate with a thickness of 211 was obtained by hot forging at a temperature of 1200°C and hot rolling at a temperature of 1200 to 1000°C, and then held at a temperature of 1200°C for 0.5 hours. After that, solution treatment was performed under air-cooling conditions, and then the plate material with the dimensions of width: 100 mm x thickness: 2 mm x length: 200 mm after solution treatment was blasted using a shot blasting machine (diameter: 2 mm).
After applying surface strain by shot blasting for the time shown in Table 1, aging treatment was carried out in the atmosphere at the temperature also shown in Table 1 (holding for 1 hour). Then, methods 1 to 22 of the present invention were carried out by performing air cooling).

つぎに、この本発明法1〜22によって得られた板材(
以下本発明板材という)および上記ショツトブラスト処
理前の板材、すなわち溶体化処理後の板材(以下従来板
材という)Kついて、大越式摩耗試験機を用い。
Next, the plate materials (
An Okoshi type abrasion tester was used for the plate material K (hereinafter referred to as the present invention plate material) and the plate material before shot blasting, that is, the plate material after solution treatment (hereinafter referred to as conventional plate material).

相手材:JIS−8UJ−2(硬さ: HRC60) 
Mating material: JIS-8UJ-2 (hardness: HRC60)
.

荷重:18.2kg、 摩擦速度:0.119m/冠。Load: 18.2kg, Friction speed: 0.119m/crown.

摩擦距離:100m、 潤滑剤:使用せず。Friction distance: 100m, Lubricant: Not used.

の条件で摩耗試験を行ない、比摩耗量を測定し、第1表
に示した。
A wear test was conducted under the following conditions, and the specific wear amount was measured and shown in Table 1.

また、これらの板材について、その表面部組織を金属顕
微鏡により観察したところ1本発明板材′は、いずれも
1次炭化物が素地中に、また2次炭化物が結晶粒界に分
散(7、かつ直径21μm以下の微細な2次炭化物が結
晶粒内に析出した組織をもつのに対して1従来板材は、
いずれも1次炭化物は素地中に分散するが、2次炭化物
が結晶粒界にだけ析出した組織をもつものであった。
In addition, when the surface structure of these plates was observed using a metallurgical microscope, it was found that the plates of the present invention had primary carbides dispersed in the matrix, and secondary carbides dispersed in the grain boundaries (7, and the diameter 1 Conventional plate material has a structure in which fine secondary carbides of 21 μm or less are precipitated within the crystal grains.
In all cases, primary carbides were dispersed in the matrix, but secondary carbides were precipitated only at grain boundaries.

〔発明の効果〕〔Effect of the invention〕

第1表に示される結果から1本発明法によって製造され
た本発明板材とおいては1いずれも特に表面部が、微細
な2次炭化物が結晶粒内に析出した組織をもつので、2
次炭化物が結晶粒界だけに析出した組織を有する溶体化
処理ままの従来板材に比してすぐれた耐摩耗性を示すこ
とが明らかである。
From the results shown in Table 1, it can be concluded that: 1) The plate materials of the present invention manufactured by the method of the present invention have a structure in which fine secondary carbides are precipitated within the crystal grains, especially on the surface;
It is clear that this material exhibits superior wear resistance compared to the conventional sheet material as solution-treated, which has a structure in which subcarbides are precipitated only at grain boundaries.

上述のように、この発明の方法によれば、直径21μm
以下の微細な2次炭化物が結晶粒内に析出した表面部組
織を有するCo基合金部材を製造することができ、前記
2次炭化物の析出によって結晶粒自体の硬さが著しく向
上するようになるので。
As mentioned above, according to the method of the present invention, a diameter of 21 μm
It is possible to produce a Co-based alloy member having a surface structure in which the following fine secondary carbides are precipitated within the crystal grains, and the hardness of the crystal grains themselves is significantly improved by the precipitation of the secondary carbides. So.

前記Co基合金部材はきわめてすぐれた耐摩耗性を示す
ようになるなど工業上有用な効果がもたらされるのであ
る。
The Co-based alloy member exhibits industrially useful effects such as extremely excellent wear resistance.

Claims (2)

【特許請求の範囲】[Claims] (1)C:0.05〜2%、 WおよびMoのうちの1種または2種:2〜20%、 Cr:15〜35%、 を含有し、残りがCoと不可避不純物からなる組成(以
上重量%)を有するCo基合金部材に、通常の条件で溶
体化処理を施した後、これにショットブラストによる表
面歪を付与し、引続いて700〜1000℃の温度で時
効処理を施すことによつて、その少なくとも表面部の組
織を、素地中に1次炭化物が、また結晶粒界に2次炭化
物が分散し、かつ結晶粒内に直径:1μm以下の2次炭
化物が分散した組織とすることを特徴とする耐摩耗性の
すぐれたCo基合金部材の製造法。
(1) A composition containing C: 0.05-2%, one or two of W and Mo: 2-20%, Cr: 15-35%, and the remainder consisting of Co and inevitable impurities ( (wt% or more) is subjected to solution treatment under normal conditions, then subjected to surface strain by shot blasting, and subsequently subjected to aging treatment at a temperature of 700 to 1000°C. As a result, the structure of at least the surface part is defined as a structure in which primary carbides are dispersed in the matrix, secondary carbides are dispersed in the grain boundaries, and secondary carbides with a diameter of 1 μm or less are dispersed in the crystal grains. A method for producing a Co-based alloy member having excellent wear resistance.
(2)C:0.05〜2%、 WおよびMoのうちの1種または2種:2〜20%、 Cr:15〜35%、 を含有し、さらに、 NiおよびFeのうちの1種または2種:1〜25%、 を含有し、残りがCoと不可避不純物からなる組成(以
上重量%)を有するCo基合金部材に、通常の条件で溶
体化処理を施した後、これにショットブラストによる表
面歪を付与し、引続いて700〜1000℃の温度で時
効処理を施すことによつて、その少なくとも表面部の組
織を、素地中に1次炭化物が、また結晶粒界に2次炭化
物が分散し、かつ結晶粒内に直径:1μm以下の2次炭
化物が分散した組織とすることを特徴とする耐摩耗性の
すぐれたCo基合金部材の製造法。
(2) Contains C: 0.05-2%, one or two of W and Mo: 2-20%, Cr: 15-35%, and further contains one of Ni and Fe. or type 2: 1 to 25%, and the remainder is Co and unavoidable impurities (weight%). After solution treatment is carried out under normal conditions, this is shot. By imparting surface strain by blasting and subsequently aging at a temperature of 700 to 1000°C, the structure at least on the surface can be changed to include primary carbides in the matrix and secondary carbides in the grain boundaries. A method for producing a Co-based alloy member with excellent wear resistance, characterized by forming a structure in which carbides are dispersed and secondary carbides with a diameter of 1 μm or less are dispersed within crystal grains.
JP17475085A 1985-08-08 1985-08-08 Manufacture of co base alloy member superior in wear resistance Granted JPS6237356A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17475085A JPS6237356A (en) 1985-08-08 1985-08-08 Manufacture of co base alloy member superior in wear resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17475085A JPS6237356A (en) 1985-08-08 1985-08-08 Manufacture of co base alloy member superior in wear resistance

Publications (2)

Publication Number Publication Date
JPS6237356A true JPS6237356A (en) 1987-02-18
JPS634906B2 JPS634906B2 (en) 1988-02-01

Family

ID=15984026

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17475085A Granted JPS6237356A (en) 1985-08-08 1985-08-08 Manufacture of co base alloy member superior in wear resistance

Country Status (1)

Country Link
JP (1) JPS6237356A (en)

Also Published As

Publication number Publication date
JPS634906B2 (en) 1988-02-01

Similar Documents

Publication Publication Date Title
EP2770080B1 (en) Nickel-base alloys and methods of heat treating nickel base alloys
JP6150192B2 (en) Method for producing Ni-base superalloy
Smith et al. The role of niobium in wrought precipitation-hardened nickel-base alloys
WO2016152982A1 (en) PRODUCTION METHOD FOR Ni-BASED SUPER HEAT-RESISTANT ALLOY
JP6826879B2 (en) Manufacturing method of Ni-based super heat-resistant alloy
JP6826766B1 (en) Manufacturing method of Ni-based super heat-resistant alloy and Ni-based super heat-resistant alloy
JPH02247345A (en) Improved titanium-aluminum alloy
JP2003027171A (en) Wear resistant aluminum alloy long-length body, production method therefor and piston for car air conditioner
US2519406A (en) Wrought alloy
US2829048A (en) High damping alloy and members prepared therefrom
JP2007009279A (en) Ni-Fe-BASE ALLOY, AND METHOD FOR MANUFACTURING Ni-Fe-BASE ALLOY MATERIAL
JP7233659B2 (en) Titanium aluminide alloy material for hot forging, method for forging titanium aluminide alloy material, and forged body
JPH02277745A (en) High hardness and high toughness cold tool steel
JPS5815529B2 (en) Setsusaku Kougu Oyobi Sonoseizouhou
JPH093604A (en) High speed tool steel for precision casting
JPS6223951A (en) Co-base alloy excellent in wear resistance
JPS6237356A (en) Manufacture of co base alloy member superior in wear resistance
JPS634905B2 (en)
JPS6237354A (en) Manufacture of co base alloy plate material superior in wear resistance
JPS635464B2 (en)
JPH10298682A (en) Heat resistant alloy, production of heat resistant alloy, and heat resistant alloy parts
US4049432A (en) High strength ferritic alloy-D53
US2677610A (en) High temperature alloy steel and articles made therefrom
JPH10237609A (en) Production of precipitation strengthening nickel-iron-base superalloy
JP2697242B2 (en) Continuous casting mold material made of Cu alloy having high cooling ability and method for producing the same