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JPH0372148B2 - - Google Patents
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JPH0372148B2 - - Google Patents

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Publication number
JPH0372148B2
JPH0372148B2 JP59064542A JP6454284A JPH0372148B2 JP H0372148 B2 JPH0372148 B2 JP H0372148B2 JP 59064542 A JP59064542 A JP 59064542A JP 6454284 A JP6454284 A JP 6454284A JP H0372148 B2 JPH0372148 B2 JP H0372148B2
Authority
JP
Japan
Prior art keywords
weight
powder
iron
alloy
chromium
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 - Lifetime
Application number
JP59064542A
Other languages
Japanese (ja)
Other versions
JPS60208448A (en
Inventor
Hiroshi Ito
Ryozo Nakamura
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.)
Nippon Tungsten Co Ltd
Original Assignee
Nippon Tungsten Co Ltd
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 Nippon Tungsten Co Ltd filed Critical Nippon Tungsten Co Ltd
Priority to JP59064542A priority Critical patent/JPS60208448A/en
Publication of JPS60208448A publication Critical patent/JPS60208448A/en
Publication of JPH0372148B2 publication Critical patent/JPH0372148B2/ja
Granted legal-status Critical Current

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  • Powder Metallurgy (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、耐摩耗部材として好適に使用できる
超硬合金とその製造方法に関する。 〔技術的背景〕 従来、WCを主体とする超硬合金は、WC−Co
系のものが主に用いられているが、結合材がCo
であるため耐摩耗性において不十分である。この
耐摩耗性を改良するために、結合材として鉄合金
を用いることも考えられるが、FeがWC中のCを
固溶することによりWC自体の脱炭作用を生じ、
合金を脆化させ、脆化部の脱落磨耗が起こり易
い。また、その他の耐摩耗性改善のための手段と
して、VC,TaC,Cr3C2等の炭化物を1%前後
添加して焼結時の結晶粒の成長を防ぎ硬度を上げ
ることも試みられているが、飛躍的な改善は望め
ないのが現状である。 〔発明の目的〕 本発明の目的は、従来のCoに代えて、焼結に
際してWCの脱炭を生じることがない高硬度の鉄
合金を結合材として用いることによつて、耐摩耗
性を改善した超硬合金とその製造方法を提供する
ことにある。 〔発明の構成〕 本発明は、炭化タングステン70〜90重量%と残
部が結合材合金とからなり、同結合材合金がクロ
ム25〜30重量%と炭素2〜5重量%と残部が鉄か
らなる鉄合金であり、且つ、同結合材合金には二
炭化三クロムが分散せしめたことによつてその目
的を達成した。 そして、製造に当たつては、WCとともにWC
の脱炭を生じることないクロムを25〜30重量%と
炭素を2〜5重量%含有するFe合金粉末が使用
される。超硬合金のWC含有量が90wt%を超える
と、機械的強度が低下することに起因するWC粒
子の脱落により耐摩耗性が低下し、また、70wt
%未満では硬質相であるWCの量が少なくなりす
ぎて耐摩耗性が低下する。そのためWCの量は70
〜90wt%が望ましい。 CrはCとともにFe中に固溶して基地を強化す
るとともに一部Cと結合してCr3C2を生じて、基
地中に析出分散して耐摩耗性を増大する。そのた
めには結合材中に25重量%存在することが必要で
ある。しかしながら、30重量%を超えるとCr3C2
の析出量が多くなつて基地を脆くするので、それ
以下に抑える必要がある。 また、Cは上記のFe中への固溶とCr3C2形成の
他に、WCの脱炭防止のために添加される。この
目的のためには最低2重量%が必要であるが、5
重量%を超えると焼結性が悪くなるのでそれ以下
に抑える必要がある。 結合金属相中に全体にCr3C2を分散させるため
には、Cr,C,Feなどの各成分単体を粉末状で
添加することもできるが、単体粉末に代えてこれ
らの合金、Cr3C2のような化合物、高クロム鋳鉄
などを所定成分になるように任意添加する方が、
本発明の炭化タングステン−鉄系超硬合金として
は組織が均一で微細なものになり、耐摩耗性が向
上する効果が大きい。 CrをCr3C2の形で加えるときは、添加C量は
Cr3C2のC量を減じておく。 焼結温度を1300〜1600℃に設定することによつ
て、結合金属中の二炭化三クロム細粒の一様な分
散が行われる。焼結温度が1300℃より低いと、焼
結密度が低く二炭化三クロムの均一な分散がしに
くくなり、また、1600℃より高くなると、結合材
合金のしみ出しが大きくなり、二炭化三クロムの
凝集が著しくなつて好ましくない。 これによつて焼結に当たつては、WCからの脱
炭がなく、また結合相には炭化クロムが析出存在
して耐摩耗性が向上し、超硬合金全体としての耐
摩耗性を向上することができる。 〔実施例〕 実施例 1 平均粒子径1.32μmの炭化タングステン粉末85
重量%と結合材合金形成のためのクロム粉末、鉄
粉末、カーボン粉末をそれぞれ4.05重量%、
10.62重量%、0.33重量%(結合材組成としてCr
27重量%、Fe 70.8重量%、C 2.2重量%)およ
びこれらの粉末に対し、2重量%のセチルアルコ
ールを加えボール・ミルにて充分混合する。つぎ
に、油圧プレス機を使用してプレス圧2.4t/cm2
10×30×5mmの圧粉体を作製した。この圧粉体を
10-4トールの真空中800℃に10分間保持した後、
1500℃で1時間焼結した。 得られた焼結体の密度は13.10であり、その硬
さはビツカース硬さ1780で、WC 85重量%、Co
15重量%よりなる通常の超硬合金のビツカース硬
さ1200に比べはるかに優れており耐摩耗性が優れ
たものである。 実施例 2 平均粒子径1.32μmを有する炭化タングステン
粉末に平均粒子径3.5μmを有する炭化クロム粉
末、鉄粉末、およびカーボン粉末を表1に示す割
合に配合し、これに2重量%のセチルアルコール
を添加し、ボボール・ミルで5時間混合した。 このあと、プレス圧2.4t/cm2で10×30×5mmの
圧粉体を作製し、10-4トールの真空中で同表に記
載の温度で1時間焼結し、焼結後同表に示す通り
の特性を得た。 実施例 3 平均粒子径1.32μmを有する炭化タングステン
粉末に、クロムを27重量%含有する−320メツシ
ユの粒度のクロム鋳鉄粉末を表2に示す割合で配
合し、これを実施例2と同一条件で混合、成形
し、この圧粉体を10-4トールの真空中で同表に示
す温度で焼結した。焼結後の特性は同表に示す通
りである。
[Industrial Application Field] The present invention relates to a cemented carbide that can be suitably used as a wear-resistant member and a method for producing the same. [Technical background] Conventionally, cemented carbide mainly made of WC was WC-Co.
Co-based materials are mainly used, but the binding material is Co
Therefore, the wear resistance is insufficient. In order to improve this wear resistance, it is possible to use an iron alloy as a binder, but Fe causes solid solution of C in WC, which causes a decarburization effect on the WC itself.
It embrittles the alloy, and the embrittled parts are likely to fall off and wear out. In addition, as another means of improving wear resistance, attempts have been made to add around 1% of carbides such as VC, TaC, and Cr3C2 to prevent grain growth during sintering and increase hardness. However, the current situation is that dramatic improvements cannot be expected. [Object of the Invention] The object of the present invention is to improve wear resistance by using a high-hardness iron alloy that does not cause decarburization of WC during sintering as a binder instead of conventional Co. The object of the present invention is to provide a cemented carbide and a manufacturing method thereof. [Structure of the Invention] The present invention consists of 70 to 90% by weight of tungsten carbide and the balance is a binder alloy, and the binder alloy consists of 25 to 30% by weight of chromium, 2 to 5% by weight of carbon, and the balance is iron. This purpose was achieved by being an iron alloy and having trichromium dicarbide dispersed in the binder alloy. In manufacturing, WC as well as WC
Fe alloy powder containing 25 to 30% by weight of chromium and 2 to 5% by weight of carbon without causing decarburization is used. When the WC content of cemented carbide exceeds 90wt%, the wear resistance decreases due to the shedding of WC particles, which is caused by the decrease in mechanical strength.
If it is less than %, the amount of WC, which is a hard phase, will be too small and the wear resistance will decrease. Therefore, the amount of WC is 70
~90wt% is desirable. Cr forms a solid solution in Fe together with C to strengthen the base, and also partially combines with C to produce Cr 3 C 2 which is precipitated and dispersed in the base to increase wear resistance. For this purpose, it is necessary that it be present in the binder in an amount of 25% by weight. However, if it exceeds 30% by weight, Cr 3 C 2
Since the amount of precipitation increases and makes the base brittle, it is necessary to keep it below this amount. Further, in addition to the solid solution in Fe and the formation of Cr 3 C 2 described above, C is added to prevent decarburization of WC. A minimum of 2% by weight is required for this purpose, but 5%
If it exceeds % by weight, sinterability will deteriorate, so it is necessary to keep it below that range. In order to disperse Cr 3 C 2 throughout the bonded metal phase, individual components such as Cr, C, and Fe can be added in powder form, but alloys of these, Cr 3 It is better to optionally add compounds such as C2 , high chromium cast iron, etc. to the specified composition.
The tungsten carbide-iron cemented carbide of the present invention has a uniform and fine structure, which has a significant effect of improving wear resistance. When adding Cr in the form of Cr 3 C 2 , the amount of C added is
Reduce the amount of C in Cr 3 C 2 . By setting the sintering temperature to 1300-1600°C, uniform dispersion of the trichromium dicarbide fine particles in the bond metal is achieved. If the sintering temperature is lower than 1300℃, the sintered density will be low and it will be difficult to uniformly disperse trichromium dicarbide.If the sintering temperature is higher than 1600℃, the binder alloy will seep out and the trichromium dicarbide will This is not preferable because the aggregation becomes significant. As a result, during sintering, there is no decarburization from the WC, and chromium carbide precipitates in the binder phase, improving wear resistance and improving the wear resistance of the cemented carbide as a whole. can do. [Example] Example 1 Tungsten carbide powder 85 with an average particle size of 1.32 μm
chromium powder, iron powder, carbon powder for alloy formation with 4.05 wt% each,
10.62% by weight, 0.33% by weight (Cr as binder composition)
27% by weight, 70.8% by weight of Fe, 2.2% by weight of C) and 2% by weight of cetyl alcohol were added to these powders and thoroughly mixed in a ball mill. Next, using a hydraulic press machine, press at a pressure of 2.4t/ cm2.
A green compact of 10 x 30 x 5 mm was produced. This compacted powder
After holding at 800°C for 10 minutes in a vacuum of 10 -4 Torr,
It was sintered at 1500°C for 1 hour. The density of the obtained sintered body was 13.10, the hardness was 1780 on the Bitkers hardness, WC was 85% by weight, Co
It has excellent wear resistance and is far superior to the Bitkers hardness of 1200, which is the standard cemented carbide made of 15% by weight. Example 2 Tungsten carbide powder having an average particle size of 1.32 μm, chromium carbide powder having an average particle size of 3.5 μm, iron powder, and carbon powder were blended in the proportions shown in Table 1, and 2% by weight of cetyl alcohol was added to this. and mixed in a Bobor mill for 5 hours. After this, a compact of 10 x 30 x 5 mm was produced with a press pressure of 2.4 t/cm 2 and sintered in a vacuum of 10 -4 Torr at the temperature listed in the same table for 1 hour. The characteristics shown in the figure were obtained. Example 3 Chromium cast iron powder with a grain size of -320 mesh containing 27% by weight of chromium was blended with tungsten carbide powder having an average particle size of 1.32 μm in the proportions shown in Table 2, and this was mixed under the same conditions as in Example 2. The powder compact was mixed and shaped, and the green compact was sintered in a vacuum of 10 -4 Torr at the temperature shown in the table. The properties after sintering are shown in the same table.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

上記実施例3によつて得た焼結体を、下記の条
件下で摩耗試験にかけた結果、添付図に示す結果
を得た。 摩耗試験機:スガ平面摩耗試験機 荷重 :3Kg 研磨紙 :カーボンランダムペーパー#320 摩耗回数(往復):2400回 同図において、曲線Aと曲線Bは実施例3によ
つて得た表2の(3)と(4)による焼結体の場合を示
し、曲線Cと曲線Dはそれぞれ15重量%Coによ
つて結合した従来のWC−Co系焼結体と同18重量
%Coによつて結合したWC−Co系焼結体の摩耗
試験結果を示す。 この図によつて本発明による焼結体の耐摩耗性
は、極めて優れており、コバルトを結合材として
含む炭化タングステン基超硬合金の2倍以上の耐
摩耗性を有することが判る。
The sintered body obtained in Example 3 above was subjected to an abrasion test under the following conditions, and the results shown in the attached drawings were obtained. Abrasion tester: Suga flat abrasion tester Load: 3Kg Abrasive paper: Carbon random paper #320 Number of abrasion (back and forth): 2400 times In the same figure, curves A and B are shown in Table 2 obtained by Example 3 ( The cases of sintered bodies according to 3) and (4) are shown, and curves C and D respectively show the case of the conventional WC-Co sintered body which is bonded by 15 wt% Co and the same which is bonded by 18 wt% Co. The results of the wear test of the WC-Co based sintered body are shown below. This figure shows that the sintered body according to the present invention has extremely excellent wear resistance, which is more than twice as high as that of tungsten carbide-based cemented carbide containing cobalt as a binder.

【図面の簡単な説明】[Brief explanation of drawings]

添付図は本発明の焼結体の耐摩耗特性を示すも
のである。
The attached figure shows the wear resistance properties of the sintered body of the present invention.

Claims (1)

【特許請求の範囲】 1 炭化タングステン70〜90重量%と残部が結合
材合金とからなり、同結合材合金がクロム25〜30
重量%と炭素2〜5重量%と残部が鉄からなる鉄
合金であり、且つ、同結合材合金には二炭化三ク
ロムが分散していることを特徴とする炭化タング
ステン−鉄系超硬合金。 2 炭化タングステン粉末70〜90重量%に、残部
がクロム25〜30重量%と炭素2〜5重量%を含有
する鉄合金からなる結合材合金を形成する炭化ク
ロム粉末とカーボン粉末と鉄粉末または高クロム
鋳鉄粉末とを配合し、同配合物を混合、圧縮成形
した後、真空中または非酸化性雰囲気中で1300〜
1600℃で焼結して、結合材合金中に二炭化三クロ
ムを形成し均一に分散することを特徴とする炭化
タングステン−鉄系超硬合金の製造方法。
[Claims] 1. Consisting of 70 to 90% by weight of tungsten carbide and the balance being a binder alloy, the binder alloy containing 25 to 30% by weight of chromium.
A tungsten carbide-iron cemented carbide, which is an iron alloy consisting of 2 to 5% by weight of carbon and the balance iron, and is characterized in that trichromium dicarbide is dispersed in the binder alloy. . 2 Chromium carbide powder, carbon powder and iron powder or high-carbon powder to form a binder alloy consisting of iron alloy containing 70 to 90% by weight of tungsten carbide powder, the balance being 25 to 30% by weight of chromium and 2 to 5% by weight of carbon. After mixing and compression molding the same compound with chrome cast iron powder, it is heated to 1300 ~
A method for producing a tungsten carbide-iron cemented carbide, which is characterized by sintering at 1600°C to form and uniformly disperse trichromium dicarbide in a binder alloy.
JP59064542A 1984-03-30 1984-03-30 Tungsten carbide-ferrous cemented carbide and its manufacturing method Granted JPS60208448A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59064542A JPS60208448A (en) 1984-03-30 1984-03-30 Tungsten carbide-ferrous cemented carbide and its manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59064542A JPS60208448A (en) 1984-03-30 1984-03-30 Tungsten carbide-ferrous cemented carbide and its manufacturing method

Publications (2)

Publication Number Publication Date
JPS60208448A JPS60208448A (en) 1985-10-21
JPH0372148B2 true JPH0372148B2 (en) 1991-11-15

Family

ID=13261210

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59064542A Granted JPS60208448A (en) 1984-03-30 1984-03-30 Tungsten carbide-ferrous cemented carbide and its manufacturing method

Country Status (1)

Country Link
JP (1) JPS60208448A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6369938A (en) * 1986-09-11 1988-03-30 Nippon Tungsten Co Ltd Sintered hard alloy excellent in sliding characteristic to sic
GB202204522D0 (en) * 2022-03-30 2022-05-11 Element Six Gmbh Cemented carbide material

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58217657A (en) * 1982-06-08 1983-12-17 Hitachi Metals Ltd Super hard alloy

Also Published As

Publication number Publication date
JPS60208448A (en) 1985-10-21

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