JP3519152B2 - WC particle-dispersed W-reinforced Ni-based alloy and composite material using the same - Google Patents
WC particle-dispersed W-reinforced Ni-based alloy and composite material using the sameInfo
- Publication number
- JP3519152B2 JP3519152B2 JP00710295A JP710295A JP3519152B2 JP 3519152 B2 JP3519152 B2 JP 3519152B2 JP 00710295 A JP00710295 A JP 00710295A JP 710295 A JP710295 A JP 710295A JP 3519152 B2 JP3519152 B2 JP 3519152B2
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- Prior art keywords
- alloy
- based alloy
- dispersed
- particle
- reinforced
- Prior art date
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- Expired - Lifetime
Links
- 239000000956 alloy Substances 0.000 title claims description 75
- 229910045601 alloy Inorganic materials 0.000 title claims description 74
- 239000002131 composite material Substances 0.000 title claims description 16
- 229910000831 Steel Inorganic materials 0.000 claims description 27
- 239000010959 steel Substances 0.000 claims description 27
- 239000002245 particle Substances 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 description 33
- 238000005245 sintering Methods 0.000 description 26
- 230000007797 corrosion Effects 0.000 description 18
- 238000005260 corrosion Methods 0.000 description 18
- 239000000843 powder Substances 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000013329 compounding Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000007791 liquid phase Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000005452 bending Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000000280 densification Methods 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 238000010137 moulding (plastic) Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000002542 deteriorative effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- 229910017318 Mo—Ni Inorganic materials 0.000 description 1
- 229910008071 Si-Ni Inorganic materials 0.000 description 1
- 229910006300 Si—Ni Inorganic materials 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009689 gas atomisation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000001513 hot isostatic pressing Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000007751 thermal spraying Methods 0.000 description 1
- 238000009692 water atomization Methods 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、WC粒子分散W強化N
i基合金およびこれを用いた複合材に係り、特に耐蝕
性、耐摩耗性および強度が同時に要求される機械部材に
適用するのに好適な合金および複合材に関する。FIELD OF THE INVENTION The present invention relates to a WC particle-dispersed W-reinforced N
The present invention relates to an i-based alloy and a composite material using the i-based alloy, and particularly to an alloy and a composite material suitable for application to a mechanical member that requires corrosion resistance, wear resistance and strength at the same time.
【0002】[0002]
【従来の技術】従来から、Ni−Cr−B−Si等のN
i基自溶合金は、耐蝕性および耐摩耗性に優れ、鋼材表
面の硬化材料として広く知られている。2. Description of the Related Art Conventionally, N such as Ni--Cr--B--Si is used.
The i-based self-fluxing alloy has excellent corrosion resistance and wear resistance, and is widely known as a hardening material for steel surface.
【0003】また、例えば特開昭62−197264号
公報には、前記Ni基自溶合金にWC粒子を微細に分散
させたWC粒子分散Ni基自溶合金が開示されており、
この合金は耐蝕性および耐摩耗性に優れているため、プ
ラスチック成形機のバレル等の機械部品に使われてい
る。Further, for example, Japanese Patent Laid-Open No. 62-197264 discloses a WC particle-dispersed Ni-based self-fluxing alloy in which WC particles are finely dispersed in the Ni-based self-fluxing alloy.
Since this alloy has excellent corrosion resistance and wear resistance, it is used for machine parts such as barrels of plastic molding machines.
【0004】また、例えば特公平5−5889号公報に
は、Mo2 NiB2 を主体とした硬質層をNi基の結合
相によって結合したMo−Ni系複硼化物合金が開示さ
れており、この合金は、耐蝕性および耐摩耗性が優れて
いるため、高腐蝕環境下で使用される材料として適して
いると言われている。Further, for example, Japanese Patent Publication No. 5-5889 discloses a Mo-Ni-based boride alloy in which a hard layer mainly composed of Mo 2 NiB 2 is bonded by a Ni-based bonding phase. Since the alloy has excellent corrosion resistance and wear resistance, it is said to be suitable as a material used in a highly corrosive environment.
【0005】さらに、例えば特開平6−57360号公
報には、Cr−Mo−W−V−B−Si−Ni等の耐蝕
耐摩耗Ni基合金が開示されており、耐蝕性および耐摩
耗性を必要とする各種構成材料として有用であると言わ
れている。Further, for example, Japanese Patent Application Laid-Open No. 6-57360 discloses a corrosion-resistant and wear-resistant Ni-based alloy such as Cr-Mo-W-V-B-Si-Ni, which has excellent corrosion resistance and wear resistance. It is said to be useful as various necessary constituent materials.
【0006】[0006]
【発明が解決しようとする課題】前記従来の各種合金の
うち、Ni基自溶合金は、耐蝕性および耐摩耗性が必ず
しも充分ではなく、材料の強度、抗折力は約0.8GP
aと小さい。このため高い応力がかかる機械部品として
は使用できないという問題がある。Among the various conventional alloys mentioned above, Ni-based self-fluxing alloys do not necessarily have sufficient corrosion resistance and wear resistance, and the strength and bending strength of the material are about 0.8 GP.
It is as small as a. For this reason, there is a problem that it cannot be used as a mechanical component to which high stress is applied.
【0007】また、WC粒子分散Ni基自溶合金は、均
一に分散しているWCのために優れた耐摩耗性および耐
蝕性が得られるが、材料の強度は約0.9GPaの抗折
力で小さい。このため、Ni基自溶合金と同様、高負荷
機械部品には使用が難しいという問題がある。Further, the WC particle-dispersed Ni-based self-fluxing alloy has excellent wear resistance and corrosion resistance because of the uniformly dispersed WC, but the strength of the material is about 0.9 GPa. And small. Therefore, like the Ni-based self-fluxing alloy, there is a problem that it is difficult to use for high-load mechanical parts.
【0008】また、Mo−Ni系複硼化物合金は、耐蝕
性および耐摩耗性には優れているが、材料の強度、抗折
力が1.5GPaで稍低く、必ずしも充分とは言えな
い。また、焼結温度が1125〜1225℃と高く、こ
の温度では鋼材の結晶粒粗大化により鋼材が劣化するた
め、焼結と同時に鋼材と接合して複合材料として用いる
には不向きであるという問題がある。Further, the Mo--Ni type double boride alloy is excellent in corrosion resistance and wear resistance, but the strength and transverse rupture strength of the material are 1.5 GPa, which is low, and is not always sufficient. In addition, the sintering temperature is as high as 1125 to 1225 ° C., and at this temperature, the steel material deteriorates due to the coarsening of the crystal grains of the steel material. is there.
【0009】さらに、耐蝕耐摩耗Ni基合金は、硬さが
低く耐摩耗性が必ずしも充分とは言えないという問題が
ある。Further, the corrosion-resistant and wear-resistant Ni-based alloy has a problem that it has low hardness and is not always sufficient in wear resistance.
【0010】本発明は、このような点を考慮してなされ
たもので、耐蝕性および耐摩耗性に優れ、しかも充分な
強度が得られるWC粒子分散W強化Ni基合金を提供す
ることを目的とする。The present invention has been made in view of the above points, and an object thereof is to provide a WC particle-dispersed W-reinforced Ni-based alloy which is excellent in corrosion resistance and wear resistance, and can obtain sufficient strength. And
【0011】本発明の他の目的は、基材の鉄鋼を劣化さ
せることなく、焼結と接合とを同時に行なって複合化す
ることができるWC粒子分散W強化Ni基合金を用いた
複合材を提供するにある。Another object of the present invention is to provide a composite material using a WC particle-dispersed W-reinforced Ni-based alloy which can be composited by simultaneously performing sintering and joining without deteriorating the steel of the base material. To provide.
【0012】[0012]
【課題を解決するための手段および作用】本発明のWC
粒子分散W強化Ni基合金は、WC粒子が10〜60重
量%分散する合金で、Bが0.5〜2.5重量%、Si
が0.4〜3.8重量%、Wが20〜35重量%、残部
Niおよび不可避的不純物からなることを特徴とする。Means and Actions for Solving the Problems WC of the Present Invention
The particle-dispersed W-reinforced Ni-based alloy is an alloy in which WC particles are dispersed in an amount of 10 to 60% by weight, B is 0.5 to 2.5% by weight, and Si is
Is 0.4 to 3.8% by weight, W is 20 to 35% by weight, and the balance is Ni and inevitable impurities.
【0013】そして、前記Ni基合金の各成分含有量
は、Bが0.8〜1.6重量%、Siが1.0〜3.2
重量%、Wが28〜32重量%、WC粒子が20〜40
重量%であることが最も好ましい。The content of each component of the Ni-based alloy is 0.8 to 1.6% by weight for B and 1.0 to 3.2 for Si.
Wt%, W 28-32 wt%, WC particles 20-40
Most preferably it is wt%.
【0014】また、本発明のWC粒子分散W強化Ni基
合金を用いた複合材は、前記化学組成のNi基合金と鉄
鋼とを接合して複合化したことを特徴とする。Further, the composite material using the WC particle-dispersed W-reinforced Ni-based alloy of the present invention is characterized in that the Ni-based alloy having the above-mentioned chemical composition is joined with steel to form a composite.
【0015】本発明のNi基合金の成分限定理由は次の
とおりである。
B:0.5〜2.5重量%(以下単に%と表す)
Bは、本合金の焼結温度を低下させ、またNi、Wと硼
化物を形成して、合金の耐摩耗性を高めるために用いら
れる。このB含有量は、多くても少なくても抗折力を低
下させるので、0.5〜2.5%、好ましくは0.7〜
2.2%とする。
Si:0〜3.8%
SiはBとともに本合金の焼結温度を低下させるために
用いられる。このため、鋼材と焼結・接合する際に、鋼
材を劣化させることなく両者を冶金的結合させるのに効
果がある。本合金では、Si量の増加とともに焼結温度
が低下するが、3.3%を超えると、逆に焼結温度が上
昇して強度が低下する傾向となり、3.8%を超える
と、合金の緻密化が妨げられて急激に強度低下を来たす
ので、上限は3.8%とする。The reasons for limiting the components of the Ni-based alloy of the present invention are as follows. B: 0.5 to 2.5 wt% (hereinafter simply referred to as%) B lowers the sintering temperature of the present alloy and forms borides with Ni and W to enhance the wear resistance of the alloy. Used for. If the B content is large or small, the transverse rupture strength is lowered, so 0.5 to 2.5%, preferably 0.7 to
2.2%. Si: 0 to 3.8% Si is used together with B to lower the sintering temperature of the present alloy. Therefore, when sintering and joining the steel material, it is effective to metallurgically bond the steel material without deteriorating the steel material. In this alloy, the sintering temperature decreases as the amount of Si increases, but when it exceeds 3.3%, the sintering temperature rises and the strength tends to decrease. Densification is hindered and the strength is rapidly reduced, so the upper limit is made 3.8%.
【0016】ここで、緻密化が妨げられるのは、3.8
%以上ではSiがNiへ固溶しない分が残り、未焼結S
iが残存するためであると考えられる。よって、Si含
有量は0〜3.8%、好ましくは0.4〜3.4%とす
る。
W:20〜35%
Wは、Bと微細な硼化物を形成し、合金の耐摩耗性およ
び強度を著しく高める。W含有量は、20%から上記効
果を現わし、35%を超えると抗折力を低下させ、焼結
温度を高めるので好ましくない。よって、W含有量は2
0〜35%、好ましくは25〜33%とする。
WC:10〜60%
WCは、合金中に微細に分散し、合金の耐摩耗性を高め
る。またWCの分散は、合金を分散強化して抗折力を向
上させる。WC含有量は、10%未満では上記効果が得
られず、また60%を超えると、合金中にマイクロポア
が多数発生して焼結不良となり、抗折力を低下させる。
したがって、WC含有量は10〜60%、好ましくは1
0〜50%とする。Here, the reason why densification is prevented is 3.8.
%, The amount of Si that does not form a solid solution with Ni remains, and unsintered S
It is considered that this is because i remains. Therefore, the Si content is 0 to 3.8%, preferably 0.4 to 3.4%. W: 20-35% W forms fine borides with B, and significantly increases the wear resistance and strength of the alloy. The W content exhibits the above effect from 20%, and if it exceeds 35%, the transverse rupture strength is lowered and the sintering temperature is increased, which is not preferable. Therefore, the W content is 2
0 to 35%, preferably 25 to 33%. WC: 10 to 60% WC is finely dispersed in the alloy and enhances the wear resistance of the alloy. Also, the dispersion of WC enhances the transverse rupture strength by dispersion strengthening the alloy. If the WC content is less than 10%, the above effect cannot be obtained, and if it exceeds 60%, a large number of micropores are generated in the alloy, resulting in poor sintering and deterioration of the transverse rupture strength.
Therefore, the WC content is 10 to 60%, preferably 1
0 to 50%.
【0017】以上、B、Si、WおよびWC含有量の中
で、最も優れた耐蝕性、耐摩耗性および強度を示すの
は、B:0.8〜1.6%、Si:1.0〜3.2%、
W:28〜32%、WC:20〜40%である。Among the B, Si, W and WC contents, B: 0.8 to 1.6% and Si: 1.0 show the best corrosion resistance, wear resistance and strength. ~ 3.2%,
W: 28 to 32%, WC: 20 to 40%.
【0018】本発明のNi基合金は、B、Si、W、N
iおよびWC粉、もしくはこれらの元素のうち2種以上
含む合金粉を所定量配合し、回転ボールミル等により粉
砕混合した粉末を用い、成形、焼結することによって製
造される。焼結は、真空、還元性ガス中で行なわれる
他、熱間静水圧焼結法等の他の方法で行なってもよい。
焼結温度は、合金組成によっても異なるが、1030〜
1170℃で行なわれる。温度が低いと、緻密化が完全
に行なわれず抗折力が低下し、また温度が高過ぎると、
結晶粒が粗大化して抗折力が低下するのみならず、焼結
と同時に鋼材との複合化を行う際、鋼材を劣化させる。The Ni-based alloy of the present invention comprises B, Si, W and N.
The i and WC powders, or alloy powders containing two or more of these elements are blended in a predetermined amount, and the powder is crushed and mixed by a rotary ball mill or the like, and molded and sintered. Sintering may be performed in vacuum or in a reducing gas, or may be performed by another method such as hot isostatic pressing.
Although the sintering temperature varies depending on the alloy composition, it is 1030 to
It is carried out at 1170 ° C. When the temperature is low, the densification is not completely performed and the transverse rupture strength is lowered, and when the temperature is too high,
Not only does the grain size become coarse and the transverse rupture strength decreases, but it also deteriorates the steel material when it is combined with the steel material simultaneously with sintering.
【0019】次に、本発明のNi基合金と鉄鋼材との金
属結合により複合化される複合材料の製造について説明
する。Next, the production of the composite material of the present invention, which is composited by metallic bonding of the Ni-based alloy and the steel material, will be described.
【0020】板状の鉄鋼材と本発明のNi基合金とを複
合化する場合には、Ni基合金の成形を直接接触させた
状態で焼結すると、液相の出現によって成形体の焼結が
行われると同時に鉄鋼材とNi基合金とが接合して複合
化される。When a plate-shaped steel material and the Ni-base alloy of the present invention are compounded, if the Ni-base alloy is sintered in direct contact with the compact, the compact is sintered due to the appearance of a liquid phase. At the same time, the steel material and the Ni-based alloy are joined to form a composite.
【0021】また、円筒状の鉄鋼材の外径部に本発明の
Ni基合金を接合して複合化する場合には、Ni基合金
の成形体の焼結時の収縮を見込んで、焼結最終過程での
液相の出現により、鉄鋼材とNi基合金とが複合化され
る。When the Ni-based alloy of the present invention is joined to the outer diameter portion of a cylindrical steel material to form a composite, the Ni-based alloy compact is sintered in consideration of shrinkage during sintering. Due to the appearance of the liquid phase in the final process, the steel material and the Ni-based alloy are composited.
【0022】本発明のNi基合金との複合化に用いる鉄
鋼材について述べる。The steel materials used for compounding with the Ni-based alloy of the present invention will be described.
【0023】本発明のNi基合金の膨脹係数は、9〜1
1×10-6/℃(20〜700℃)であり、これは13
%Cr鋼に近似している。複合化後の接合面の残留応力
を考慮すると、鉄鋼材としてはSUS420J2、SU
S440C、SUS430等のステンレス鋼が好まし
い。Ni基合金の成形体が単純形状の場合には、S25
C等の炭素鋼との複合化が可能である。The expansion coefficient of the Ni-based alloy of the present invention is 9 to 1
1 × 10 −6 / ° C. (20 to 700 ° C.), which is 13
It is similar to% Cr steel. Considering the residual stress of the joint surface after compounding, as the steel material, SUS420J2, SU
Stainless steel such as S440C and SUS430 is preferable. If the Ni-based alloy compact has a simple shape, S25
Composite with carbon steel such as C is possible.
【0024】本発明のNi基合金と鉄鋼材との複合化の
方法としては、Ni基合金と同一の組成の合金粉を予め
水アトマイズ法やガスアトマイズ法などによって製造
し、その合金粉末を用いて、溶射、再溶融あるいは肉盛
をすることによっても可能である。As a method for compounding the Ni-based alloy and the steel material of the present invention, alloy powder having the same composition as the Ni-based alloy is previously produced by a water atomizing method or a gas atomizing method, and the alloy powder is used. It is also possible by thermal spraying, remelting or overlaying.
【0025】[0025]
【実施例】以下に、本発明を実施例によりさらに説明す
る。EXAMPLES The present invention will be further described below with reference to examples.
【0026】実施例
本発明のNi基合金を製造するに際し、表1に示す原料
粉の配合比率からなる試料番号1〜5合金粉末を配合
し、回転ボールミルによりエチルアルコール中で混合粉
砕した。次いで、この混合合金粉末を乾燥し、プレス成
形し、真空中で焼結した。 Example In producing the Ni-based alloy of the present invention, alloy powders of Sample Nos. 1 to 5 having the mixing ratios of the raw material powders shown in Table 1 were mixed and mixed and pulverized in ethyl alcohol by a rotary ball mill. The mixed alloy powder was then dried, press molded and sintered in vacuum.
【0027】[0027]
【表1】
本発明合金の試料番号1〜5の焼結温度を、表2に示
す。焼結時間は、いずれも10分間である。硬さ、比摩
耗量、耐蝕性、抗折力の各種の性能試験を行った。これ
らの試験結果を、表2に示す。[Table 1] Table 2 shows the sintering temperatures of Sample Nos. 1 to 5 of the alloys of the present invention. The sintering time is 10 minutes in each case. Various performance tests such as hardness, specific wear amount, corrosion resistance, and transverse rupture strength were conducted. The results of these tests are shown in Table 2.
【0028】各種の性能試験の条件は、下記の通りであ
る。
(1)摩耗試験
試験機:大越式迅速摩耗試験機
試験条件:
摩擦速度 2.0m/sec
摩擦距離 600m
最終荷重 18.6kgf
相手材料 SKD11(HRC58)
(2)腐蝕試験
腐蝕液 塩酸20%溶液(22℃)
浸漬時間 5Hr
(3)抗折試験
試験方法 JIS H5501 三点曲げ抗折試験
試験片の寸法 4×8×24mm、研削加工The conditions of various performance tests are as follows. (1) Wear test tester: Ogoshi rapid wear tester Test conditions: Friction speed 2.0 m / sec Friction distance 600 m Final load 18.6 kgf Mating material SKD11 (HRC58) (2) Corrosion test Corrosion liquid 20% hydrochloric acid solution ( 22 ℃) Immersion time 5 hours (3) Bending test method JIS H5501 Three-point bending bending test Dimension of test piece 4 × 8 × 24 mm, grinding
【0029】[0029]
【表2】
本発明合金と、比較例として4種の従来例合金との焼結
温度、腐蝕減量、比摩耗量、硬度、抗折力を比較した。
その結果を、表3に示す。[Table 2] The alloy of the present invention and four conventional alloys as comparative examples were compared for sintering temperature, corrosion loss, specific wear amount, hardness and transverse rupture strength.
The results are shown in Table 3.
【0030】[0030]
【表3】
表3から分るように、本発明合金は、従来合金に比較し
て、耐蝕性、耐摩耗性に優れ、しかも高い抗折力を示し
ていることが判る。[Table 3] As can be seen from Table 3, the alloy of the present invention is superior to the conventional alloy in corrosion resistance and wear resistance, and exhibits high transverse rupture strength.
【0031】参考例1
Ni基合金の円板状成形体と鋼材との複合化を、焼結と
同時に行った参考例を以下に示す。 Reference Example 1 A reference example in which a disc-shaped compact of a Ni-based alloy and a steel material were compounded simultaneously with sintering is shown below.
【0032】Ni基合金の目標成分が、重量%で、2.
2%B、3.5%Si、25%W、残部Niになるよう
に各原料粉を配合し、回転ボールミルによりエチルアル
コール中で48時間、粉砕混合した。その後、乾燥、プ
レス成形し、図1(a)に示す形状の円板状成形体を作
成した。この成形体の寸法は、厚さ10mm、直径φ40
mm、密度は約50%であった。The target component of the Ni-based alloy is 2.
The raw material powders were blended so as to be 2% B, 3.5% Si, 25% W, and the balance Ni, and pulverized and mixed in ethyl alcohol by a rotary ball mill for 48 hours. Then, it was dried and press-molded to prepare a disk-shaped molded body having the shape shown in FIG. The size of this compact is 10 mm thick and 40 mm in diameter.
mm, the density was about 50%.
【0033】この円板状成形体を、図1(b)に示すよ
うに鋼材SUS420J2の上に載置した状態で、真空
中で1030℃、10分間焼結して、複合化を行った。
焼結体は厚さ7mm、直径φ34mmの寸法に収縮した。This disk-shaped compact was placed on a steel material SUS420J2 as shown in FIG. 1 (b) and sintered at 1030 ° C. for 10 minutes in vacuum to form a composite.
The sintered body shrank to a thickness of 7 mm and a diameter of 34 mm.
【0034】図1(c)に示すSUS420J2材と焼
結体の接触面の断面を研摩した後、光学顕微鏡で観察し
たところ、両者は強固に金属結合していることが確認さ
れた。この結合は焼結により液相が発生し、SUS42
0J2材に濡れることによって行われたと考えられる。
このように焼結、複合化された複合材料を機械加工し、
所定寸法に仕上げ、プラスチック成形機用部材として用
いた。When the cross section of the contact surface between the SUS420J2 material and the sintered body shown in FIG. 1 (c) was polished and then observed with an optical microscope, it was confirmed that both were strongly metal-bonded. A liquid phase is generated in this bond by sintering, and SUS42
It is thought that this was done by getting wet with the 0J2 material.
In this way, the composite material that is sintered and compounded is machined,
The product was finished to a predetermined size and used as a member for a plastic molding machine.
【0035】参考例2
Ni基合金の円筒外径部に鋼材を焼結、複合化した参考
例を以下に示す。 Reference Example 2 A reference example in which a steel material is sintered and compounded on the outer diameter of a cylinder of a Ni-based alloy is shown below.
【0036】Ni基合金の目標成分が、重量%で、1.
0%B、2.0%Si、20%W、残部Niになるよう
に各原料粉を配合し、回転ボールミルによりエチルアル
コール中で48時間粉砕混合した。その後、乾燥し、ラ
バープレスにより成形し、成形体を図2(a)に示す円
筒形に加工した。この成形体の寸法は、外径φ56mm、
内径φ27mm、高さ48mm、密度は約50%であった。The target component of the Ni-based alloy is 1.
The raw material powders were blended so that 0% B, 2.0% Si, 20% W and the balance Ni were obtained, and the mixture was pulverized and mixed in ethyl alcohol by a rotary ball mill for 48 hours. Then, it was dried and molded by a rubber press, and the molded body was processed into the cylindrical shape shown in FIG. The dimensions of this molded body are an outer diameter of 56 mm,
The inner diameter was 27 mm, the height was 48 mm, and the density was about 50%.
【0037】この円筒状成形体の中心に図2(b)に示
すようにSUS440C材の丸棒を挿入してセットし、
真空中で1080℃、10分間、焼結、複合化を行っ
た。SUS440C材の丸棒の外径は、成形体の焼結収
縮を見込んでφ23.0mmとした。As shown in FIG. 2 (b), a round bar of SUS440C material was inserted and set in the center of this cylindrical molded body,
Sintering and compounding were performed in vacuum at 1080 ° C. for 10 minutes. The outer diameter of the SUS440C round bar was φ23.0 mm in consideration of the sintering shrinkage of the molded body.
【0038】図2(c)に示すように、円筒状成形体は
焼結、複合化により収縮を起こし、その寸法は外径φ4
5mm、高さ40mmに収縮した。光学顕微鏡での観察によ
れば、成形体中からの液相生成により丸棒鋼材と焼結体
は強固に金属結合されている。焼結、複合化後、複合材
料は機械加工により所定の寸法に仕上げ、プラスチック
成形機用スクリュ部材として用いた。As shown in FIG. 2 (c), the cylindrical molded body shrinks due to sintering and compounding, and its dimension is an outer diameter φ4.
Shrinked to 5 mm and height 40 mm. According to the observation with an optical microscope, the round bar steel material and the sintered body are strongly metal-bonded to each other due to the liquid phase generation in the molded body. After sintering and compounding, the composite material was machined to a predetermined size and used as a screw member for a plastic molding machine.
【0039】[0039]
【発明の効果】以上説明したように本発明によれば、耐
蝕性、耐摩耗性、かつ高強度を有し、高負荷のかかる機
械部品に適した合金材料が得られた。また、本発明合金
は、焼結温度が比較的低いので鋼材との複合化を焼結と
同時に行うことができ、効率的生産、コスト面で有利で
ある。As described above, according to the present invention, an alloy material having corrosion resistance, wear resistance, and high strength, which is suitable for a machine part under high load, was obtained. Moreover, since the alloy of the present invention has a relatively low sintering temperature, it can be compounded with a steel material simultaneously with sintering, which is advantageous in terms of efficient production and cost.
【図1】Ni基合金の円板状成形体と鋼材との複合化を
焼結と同時に行う複合材料の製造法を説明した図。FIG. 1 is a diagram illustrating a method of manufacturing a composite material in which a disc-shaped compact of a Ni-based alloy and a steel material are compounded simultaneously with sintering.
【図2】Ni基合金の円板状成形体と丸棒鋼材との複合
化を焼結と同時に行う複合材料の製造法を説明した図。FIG. 2 is a diagram illustrating a method of manufacturing a composite material in which a disk-shaped compact of a Ni-based alloy and a round bar steel material are compounded simultaneously with sintering.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 梅 原 稔 静岡県沼津市大岡2068の3 東芝機械株 式会社 沼津事業所内 (56)参考文献 特開 昭48−58059(JP,A) 特開 昭62−177144(JP,A) 特開 昭62−197264(JP,A) 特開 平4−337047(JP,A) 特開 平5−214479(JP,A) 特開 平4−56745(JP,A) 特開 平2−185942(JP,A) 特開 平2−15140(JP,A) 特開 平2−156037(JP,A) 特公 昭56−30181(JP,B2) ─────────────────────────────────────────────────── ─── Continued front page (72) Inventor Minoru Umehara 2068 Ooka, Numazu City, Shizuoka Prefecture Toshiba Machine Co., Ltd. Ceremony Company Numazu Office (56) References JP-A-48-58059 (JP, A) JP 62-177144 (JP, A) JP 62-197264 (JP, A) JP-A-4-337047 (JP, A) JP-A-5-214479 (JP, A) JP-A-4-56745 (JP, A) JP-A-2-185942 (JP, A) Japanese Patent Laid-Open No. 2-15140 (JP, A) Japanese Patent Laid-Open No. 2-156037 (JP, A) Japanese Patent Sho 56-30181 (JP, B2)
Claims (6)
で、Bが0.5〜2.5重量%、Siが0.4〜3.4
重量%、Wが20〜35重量%、残部Niおよび不可避
的不純物からなることを特徴とするWC粒子分散W強化
Ni基合金。1. An alloy in which 10 to 60% by weight of WC particles are dispersed, 0.5 to 2.5% by weight of B and 0.4 to 3.4 of Si.
% Of W, 20 to 35% by weight of W, balance Ni and inevitable impurities, WC particle-dispersed W-reinforced Ni-based alloy.
ることを特徴とする請求項1記載のWC粒子分散W強化
Ni基合金。2. The WC particle-dispersed W-reinforced Ni-based alloy according to claim 1, wherein the content of B is 0.8 to 1.6% by weight.
ることを特徴とする請求項1または2記載のWC粒子分
散W強化Ni基合金。3. The WC particle-dispersed W-reinforced Ni-based alloy according to claim 1, wherein the Si content is 1.0 to 3.2% by weight.
とを特徴とする請求項1,2または3記載のWC粒子分
散W強化Ni基合金。4. The WC particle-dispersed W-reinforced Ni-based alloy according to claim 1, wherein the W content is 28 to 32% by weight.
あることを特徴とする請求項1,2,3または4記載の
WC粒子分散W強化Ni基合金。5. The WC particle-dispersed W-reinforced Ni-based alloy according to claim 1, 2, 3 or 4, wherein the amount of the WC particles dispersed is 20 to 40% by weight.
粒子分散W強化Ni基合金と鉄鋼とを接合したことを特
徴とするWC粒子分散W強化Ni基合金を用いた複合
材。6. The WC according to claim 1, 2, 3, 4 or 5.
A composite material using a WC particle-dispersed W-reinforced Ni-based alloy, characterized in that a particle-dispersed W-reinforced Ni-based alloy and steel are joined together.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP00710295A JP3519152B2 (en) | 1995-01-20 | 1995-01-20 | WC particle-dispersed W-reinforced Ni-based alloy and composite material using the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP00710295A JP3519152B2 (en) | 1995-01-20 | 1995-01-20 | WC particle-dispersed W-reinforced Ni-based alloy and composite material using the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH08199269A JPH08199269A (en) | 1996-08-06 |
| JP3519152B2 true JP3519152B2 (en) | 2004-04-12 |
Family
ID=11656730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP00710295A Expired - Lifetime JP3519152B2 (en) | 1995-01-20 | 1995-01-20 | WC particle-dispersed W-reinforced Ni-based alloy and composite material using the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3519152B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5630181B2 (en) | 2010-03-05 | 2014-11-26 | 大日本印刷株式会社 | Negative resist composition, method for producing relief pattern using the resist composition, and method for producing photomask |
-
1995
- 1995-01-20 JP JP00710295A patent/JP3519152B2/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5630181B2 (en) | 2010-03-05 | 2014-11-26 | 大日本印刷株式会社 | Negative resist composition, method for producing relief pattern using the resist composition, and method for producing photomask |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH08199269A (en) | 1996-08-06 |
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