JPS635441B2 - - Google Patents
Info
- Publication number
- JPS635441B2 JPS635441B2 JP57156392A JP15639282A JPS635441B2 JP S635441 B2 JPS635441 B2 JP S635441B2 JP 57156392 A JP57156392 A JP 57156392A JP 15639282 A JP15639282 A JP 15639282A JP S635441 B2 JPS635441 B2 JP S635441B2
- Authority
- JP
- Japan
- Prior art keywords
- less
- steel powder
- particle size
- sintered
- powder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000843 powder Substances 0.000 claims description 68
- 229910000831 Steel Inorganic materials 0.000 claims description 48
- 239000010959 steel Substances 0.000 claims description 48
- 229910045601 alloy Inorganic materials 0.000 claims description 30
- 239000000956 alloy Substances 0.000 claims description 30
- 239000002245 particle Substances 0.000 claims description 28
- 229910052802 copper Inorganic materials 0.000 claims description 6
- 238000009826 distribution Methods 0.000 claims description 6
- 229910052750 molybdenum Inorganic materials 0.000 claims description 6
- 238000005029 sieve analysis Methods 0.000 claims description 6
- 229910052721 tungsten Inorganic materials 0.000 claims description 6
- 229910052720 vanadium Inorganic materials 0.000 claims description 6
- 239000012535 impurity Substances 0.000 claims description 5
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 238000000034 method Methods 0.000 description 14
- 238000005245 sintering Methods 0.000 description 14
- 229910000851 Alloy steel Inorganic materials 0.000 description 13
- 230000000694 effects Effects 0.000 description 10
- 238000005507 spraying Methods 0.000 description 10
- 150000001247 metal acetylides Chemical class 0.000 description 9
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000004663 powder metallurgy Methods 0.000 description 4
- 238000000137 annealing Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000001000 micrograph Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229910001563 bainite Inorganic materials 0.000 description 1
- 230000037237 body shape Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000001513 hot isostatic pressing Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Description
本発明は、微細な焼結組織を有する高密度の耐
摩耗焼結合金を製造するに用いる合金鋼粉に関す
るものである。
従来、内燃機関のバルプロツカーアーム、カ
ム、タペツトなど大きな面圧が加わる摺動表面部
分またはかかる部分を有する部品には耐摩耗性チ
ル鋳鉄、熱処理鋼などが用いられてきたが、厳し
い作動条件のもとではより優れた耐久性が求めら
れるに至つている。そのため、粉末治金法により
得られるCrなどを含有する高炭素焼結合金を使
用する試みがなされている。すなわち、粉末治金
法によれば、所定の組成をもつ粉末あるいは複数
種類の粉末の混合物を金型内で成形し還元性ある
いは中性雰囲気もしくは真空中で十分収縮のおこ
る条件で焼結して、炭化物が分散した高密度の耐
摩耗焼結合金を得ることができる。
かかる焼結合金を製造するための金属粉として
は、焼結過程においてFe中に拡散しにくいCrな
どの合金成分元素を予合金の形で含有させて溶製
した溶融合金鋼を噴霧法により粉化した合金鋼粉
に拡散の容易なCなどの元素を混粉法によつて添
加したものが用いられている。溶鋼流を水その他
の液体流ジエツトによつて飛散凝固させて粉末に
する噴霧法によれば、金型成形を可能にする不規
則形状の合金鋼粉が得られる。また、従来の上述
した耐摩耗焼結合金の製造に用いられる合金鋼粉
の粒度は、従来の噴霧純鉄粉あるいは噴霧ステン
レス鋼粉、などに準じて調整されるのが通常であ
る。
上述した合金鋼粉を用いた耐摩耗焼結合金は、
炭化物を含有することによつて高い硬さを有する
が、炭化物が粗大化すると耐衝撃性が損なわれる
ため、微細組織となつていなけれならず。また、
空孔の存在は耐ピツチング性を著しく劣化させる
ため、低空孔率すなわち真密度に低い焼結密度が
要求される。しかしながら、従来の耐摩耗焼結合
金用合金鋼粉を使用して焼結を行なつた場合、こ
れらの条件を同時に満たすことは極めて困難であ
つた。すなわち、炭化物が粗大化しない程度の焼
結によつては、高い密度が得られず、逆に高密度
になるような焼結条件によると炭化物が粗大化す
るほか、焼結時の収縮が不均一になりやすく、焼
結体に歪みが生ずるという問題点があつた。
この点を克服するため、焼結鍛造法あるいは熱
間静水圧プレス法により、高密度で微細な組織を
有する耐摩耗焼結合金製品を製造することも可能
であるが、工程が複雑で生産性が劣り、高価にな
るという問題があつた。
本発明の目的は、上述した従来法による問題点
を解決して、高密度で形状歪みが小さく、微細組
織を有する焼結合金を製造するための噴霧合金鋼
粉を提供しようとするものである。
これがため、本発明による耐摩耗焼結合金用鋼
粉は、重量比でCr3〜20%、Si0.3〜2%、C0.3%
以下、N0.2%以下を含み、かつ、平均粒径が30
〜50μmの範囲にある噴霧鋼粉であることを特徴
とする。また、本発明による耐摩耗焼結合金用鋼
粉には、所要に応じて、NiおよびCuあわせて5
%以下、およびV,Mo,Wの1種または2種以
上をあわせて5%以下含有させるのが好ましい。
本発明による合金鋼粉の平均粒径は、JISR600
で1956に準拠したふるい分析による粒度分布の結
果を用いて規定される値で、+100メツシユを
161μm、−100/+150メツシユを126μm、−150/
+200メツシユを89μm、−200/+250メツシユを
68μm、−250/+325メツシユを52μm、−325メツ
シユを22μmとして算出したものである。本発明
による合金鋼粉を上述した平均粒径30〜50μmの
粒度にする方法としては、噴霧時の噴霧ジエツト
等を調整することによつて、あるいはまた、必要
に応じ、噴霧後の粉末を焼鈍し、焼鈍時に焼結凝
集した粒子を解砕して所定粒度に調整することに
よつて得られる。
また、噴霧法としては、溶鋼を水または油など
の液体流ジエツトによつて噴霧する方法であれば
よく、装置上の制約は無い。例えば、特公昭52―
19540号公報に記載の方法を採用することができ
る。
以下、本発明鋼粉の成分組成範囲の限定理由を
説明する。
Crは、焼結体にあつてFe中に固溶して基地を
強化するとともに、添加したCと焼結中に結合し
て炭化物を形成し、焼結体の硬さを増して耐摩耗
性を向上させる。また、噴霧時に溶鋼の表面エネ
ルギーを減少させ、噴霧効率が向上して、細かい
粒度の鋼粉を得られやすくする効果もあわせも
つ。Cr含有量が3%未満ではこれらの効果は小
さく、20%を超えて含有させてもそれ以上の効果
は得られない。
Siは、焼結体にあつてFe中に固溶して基地を
強化するほか、噴霧時に溶鋼の酸化を防止する効
果を有する。0.3%未満では酸化防止の効果は見
られず、2%を超えると焼結体の硬さが低下し、
耐摩耗性を損なう。
鋼粉中のCおよびNは、鋼粉の硬さを増して圧
縮性および成形性を損ねるので低く抑える必要が
ある。Cは0.3%,Nは0.2%を超えると、6t/cm2
の圧力で成形したときの圧粉密度が6g/cm3未満
となり、圧粉体強度が極めて低くなるほか、焼結
によつて95%以上の高密度比を得ることが難し
く、また、かりに高密度が得られても、焼結によ
る収縮量が大きいので焼結体の歪みが大きくな
る。なお、本発明による鋼粉を用いた耐摩耗焼結
合金にCを含有させるには、噴霧合金鋼粉に混合
法によつて添加することが必要である。
また、前述したように、本発明による合金鋼粉
に目的に応じて、NiおよびCuあわせて5%以下、
V,MoおよびWあわせて5%以下の範囲でNi,
Cu,V,Mo,およびWを含有させることができ
る。これらの元素はいずれも混合法によつて鋼粉
に添加して焼結中に十分拡散させることは難し
く、したがつて、噴霧法による合金鋼粉製造時に
予合金として含有させることが望ましい。Niお
よびCuは焼結体にあつてFe中に固溶して基地を
強化するとともに、炭化物の微細化を可能にする
が、合計量が5%を超えて含有させてもそれ以上
の効果は得られない。V,MoおよびWは焼結体
にあつてFe中に固溶して基地を強化するととも
に、添加したCと結合して炭化物を形成し、耐摩
耗性を向上させるが、合計量が5%を超えるとむ
しろ靭性を損ねる。
不可避不純物としては、溶解素材から混入する
Mn,P,S,Alなど、および、おもに噴霧中あ
るいは鋼粉焼鈍中の鋼粉の酸化によつて捕獲され
るOなどがあり、鋼粉の成形性、圧縮性および焼
結合金の耐摩耗性を損わないためにはこれらを合
計量で2%以下に限定する必要がある。
次に、鋼粉の平均粒径を30〜50μmに限定する
理由につき説明する。
水あるいは油などの液体を噴霧媒とする噴霧法
は、比較的自由に粉末の合金組成を選定すること
ができる点、および工程が簡単である点で、有利
な鋼粉製造技術である。したがつて粉末治金用と
して広く用いられているが、通常の粉末治金用鋼
粉は、いずれもふるい分析による粒度分布から求
めた平均粒径が50μmを超えたものである。とこ
ろが、炭化物分散熱の高密度焼結合金を得るため
には、このような比較的粒度の粗い鋼粉では十分
な効果が得られない。すなわち、粉末の粒度が粗
いと焼結性が悪いため、高密度の焼結合金が得ら
れにくいとともに、焼結中の合金の結晶粒も大き
いため、粒界に形成される炭化物が成長粗大化し
やすい。また、圧粉体に大きな空孔が存在するた
め、焼結中におこる収縮が等方均一に進行しにく
く、焼結体の形状歪みが大きくなる。さらに、焼
結体に大きな空孔が残存して耐ピツチング性を劣
化させる。しかも、とくに合金鋼粉にP,Bなど
を含む粉末を混合添加して焼結中に容易に液相を
生じせしめ、比較的低い温度で焼結させようとす
る場合、圧粉体の時点で存在する大きな空孔を消
失させることは難しく、P,Bなどの添加の効果
が十分発揮されないため、高い焼結密度が得られ
がたい。
これらの問題点は、噴霧鋼粉の平均粒径を
50μm以下とすることによつてはじめて解決する
ことができ、形状歪みが小さく、焼結合金断面の
600倍程度の光顕観察によつて識別される炭化物
の平均粒度が10μm以下、密度比が95%以上の焼
結合金を得ることができる。一方、鋼粉の平均粒
径を30μm以下にすると、数μm以下の微粉量が増
加し、成形時の金型かじりなどの問題が発生する
とともに、通常の噴霧装置によつて歩留り良く製
造することが困難となるため、平均粒径の下限を
30μmと定める。
以下、実施例について述べる。
特公昭52―19540号公報に記載された水噴霧装
置を用い、溶鋼ノズル径6〜14mm、水圧80〜150
Kg/cm2、水・溶鋼比3〜6/Kgの条件により所
定の組成の噴霧生鋼粉を製造し、アンモニア分解
ガス中700〜950℃で焼鈍し、乳鉢中で解砕したの
ち粒度構成し、いずれも80メツシユ以下の本発明
による合金鋼粉および比較用鋼粉を第1表のごと
くに得た。
The present invention relates to an alloy steel powder used for manufacturing a high-density, wear-resistant sintered alloy having a fine sintered structure. Conventionally, wear-resistant chilled cast iron, heat-treated steel, etc. have been used for parts with sliding surfaces that are subject to large surface pressure, such as valve locker arms, cams, and tappets of internal combustion engines, or parts that have such parts. Nowadays, even greater durability is required. Therefore, attempts have been made to use high carbon sintered alloys containing Cr etc. obtained by powder metallurgy. In other words, according to the powder metallurgy method, a powder with a predetermined composition or a mixture of multiple types of powder is molded in a mold and sintered in a reducing or neutral atmosphere or in a vacuum to cause sufficient shrinkage. , it is possible to obtain a high-density, wear-resistant sintered alloy in which carbides are dispersed. The metal powder used to produce such a sintered alloy is made by spraying molten alloy steel containing alloying elements such as Cr that are difficult to diffuse into Fe in the form of a pre-alloy during the sintering process. In this method, an element such as C, which is easily diffused, is added to alloyed steel powder using a mixed powder method. The atomization process, in which a stream of molten steel is splashed and solidified into powder by a jet of water or other liquid stream, yields alloyed steel powder of irregular shape that allows molding. Further, the particle size of the alloy steel powder used in the production of the above-mentioned conventional wear-resistant sintered alloy is usually adjusted according to the conventional atomized pure iron powder or atomized stainless steel powder. The wear-resistant sintered alloy using the above-mentioned alloy steel powder is
It has high hardness due to the inclusion of carbide, but if the carbide becomes coarse, impact resistance will be impaired, so it must have a fine structure. Also,
Since the presence of pores significantly deteriorates pitting resistance, a low porosity, that is, a low true density and a low sintered density are required. However, when sintering is performed using conventional alloy steel powder for wear-resistant sintered alloys, it is extremely difficult to simultaneously satisfy these conditions. In other words, if the carbide is sintered to the extent that it does not become coarse, high density cannot be obtained; on the other hand, if the sintering conditions are such that the carbide becomes coarse, the carbide will become coarse and shrinkage during sintering will not occur. There was a problem that the sintered body tends to become uniform, causing distortion in the sintered body. To overcome this problem, it is possible to manufacture wear-resistant sintered alloy products with a high density and fine structure using the sinter forging method or hot isostatic pressing method, but the process is complicated and productivity is low. The problem was that it was inferior and expensive. An object of the present invention is to solve the problems caused by the conventional methods described above and to provide a spray alloyed steel powder for producing a sintered alloy with high density, low shape distortion, and a fine structure. . Therefore, the steel powder for wear-resistant sintered alloys according to the present invention has a weight ratio of 3 to 20% Cr, 0.3 to 2% Si, and 0.3% C.
Contains N0.2% or less and has an average particle size of 30
It is characterized by being an atomized steel powder in the range of ~50μm. In addition, the steel powder for wear-resistant sintered alloys according to the present invention may contain a total of 50% Ni and Cu as required.
% or less, and the total content of one or more of V, Mo, and W is preferably 5% or less. The average particle size of the alloy steel powder according to the present invention is JISR600
+100 mesh with the value specified using the particle size distribution results from sieve analysis in accordance with 1956.
161μm, -100/+150 mesh to 126μm, -150/
+200 mesh is 89μm, -200/+250 mesh is
It was calculated based on the assumption that 68 μm, −250/+325 mesh is 52 μm, and −325 mesh is 22 μm. The method of making the alloy steel powder according to the present invention have the above average particle size of 30 to 50 μm is by adjusting the spray jet during spraying, or, if necessary, by annealing the powder after spraying. However, it can be obtained by crushing particles that have been sintered and agglomerated during annealing and adjusting them to a predetermined particle size. Further, the spraying method may be any method in which molten steel is sprayed with a jet of liquid such as water or oil, and there are no restrictions on the equipment. For example, special public service in Showa 52-
The method described in Publication No. 19540 can be adopted. The reason for limiting the composition range of the steel powder of the present invention will be explained below. In the sintered body, Cr dissolves in Fe to strengthen the matrix, and also combines with added C during sintering to form carbides, increasing the hardness of the sintered body and improving wear resistance. improve. It also has the effect of reducing the surface energy of molten steel during spraying, improving spray efficiency and making it easier to obtain fine-grained steel powder. If the Cr content is less than 3%, these effects will be small, and if the Cr content exceeds 20%, no further effects will be obtained. In the sintered body, Si dissolves in Fe to strengthen the matrix and also has the effect of preventing oxidation of molten steel during spraying. If it is less than 0.3%, no anti-oxidation effect is observed, and if it exceeds 2%, the hardness of the sintered body decreases.
Impairs wear resistance. C and N in the steel powder must be kept low because they increase the hardness of the steel powder and impair compressibility and formability. If C exceeds 0.3% and N exceeds 0.2%, 6t/cm 2
When compacted at a pressure of Even if the density is obtained, the amount of shrinkage due to sintering is large, resulting in large distortion of the sintered body. In order to incorporate C into the wear-resistant sintered alloy using the steel powder according to the present invention, it is necessary to add it to the spray alloyed steel powder by a mixing method. Further, as mentioned above, depending on the purpose, the alloy steel powder according to the present invention may contain 5% or less of Ni and Cu in total.
Ni within a range of 5% or less in total for V, Mo and W,
Cu, V, Mo, and W can be contained. It is difficult for any of these elements to be added to steel powder by a mixing method and sufficiently diffused during sintering, and therefore it is desirable to include them as a pre-alloy when producing alloy steel powder by a spraying method. Ni and Cu are dissolved in Fe in the sintered body to strengthen the matrix and make carbides finer, but even if the total amount exceeds 5%, there is no further effect. I can't get it. V, Mo and W form a solid solution in Fe in the sintered body to strengthen the matrix, and also combine with added C to form carbides and improve wear resistance, but the total amount is 5%. Exceeding this will actually impair toughness. Unavoidable impurities are mixed in from dissolved materials.
These include Mn, P, S, Al, etc., and O, which is mainly captured by the oxidation of steel powder during spraying or annealing, and improves the formability and compressibility of steel powder and the wear resistance of sintered alloys. In order not to impair performance, it is necessary to limit the total amount of these to 2% or less. Next, the reason for limiting the average particle size of steel powder to 30 to 50 μm will be explained. A spraying method using a liquid such as water or oil as a spraying medium is an advantageous steel powder manufacturing technique because it allows relatively free selection of the alloy composition of the powder and the process is simple. Therefore, it is widely used for powder metallurgy, but all ordinary steel powders for powder metallurgy have an average particle size exceeding 50 μm as determined from particle size distribution by sieve analysis. However, in order to obtain a high-density sintered alloy with carbide dispersion heat, a sufficient effect cannot be obtained with such comparatively coarse-grained steel powder. In other words, if the particle size of the powder is coarse, sintering properties are poor, making it difficult to obtain a high-density sintered alloy, and since the crystal grains of the alloy during sintering are also large, carbides formed at the grain boundaries will grow and become coarse. Cheap. Furthermore, since large pores are present in the green compact, shrinkage that occurs during sintering is difficult to progress uniformly, resulting in large distortions in the shape of the sintered compact. Furthermore, large pores remain in the sintered body, which deteriorates pitting resistance. Moreover, especially when mixing and adding powders containing P, B, etc. to alloy steel powder to easily generate a liquid phase during sintering and sintering at a relatively low temperature, it is necessary to mix and add powders containing P, B, etc. It is difficult to eliminate the large pores that exist, and the effects of adding P, B, etc. are not sufficiently exerted, so it is difficult to obtain a high sintered density. These problems reduce the average particle size of the atomized steel powder.
This problem can only be solved by setting the diameter to 50 μm or less, resulting in small shape distortion and a
It is possible to obtain a sintered alloy in which the average particle size of carbides identified by light microscopy observation at a magnification of about 600 times is 10 μm or less, and the density ratio is 95% or more. On the other hand, if the average particle size of steel powder is set to 30 μm or less, the amount of fine powder of several μm or less increases, causing problems such as mold galling during molding, and it is difficult to manufacture with a good yield using normal spray equipment. Therefore, the lower limit of the average particle size
Defined as 30μm. Examples will be described below. Using the water spray device described in Japanese Patent Publication No. 52-19540, the molten steel nozzle diameter is 6 to 14 mm, and the water pressure is 80 to 150.
Kg/cm 2 and a water/molten steel ratio of 3 to 6/Kg to produce atomized raw steel powder with a predetermined composition, annealed in ammonia decomposition gas at 700 to 950°C, and crushed in a mortar to determine the particle size structure. However, alloy steel powder according to the present invention and steel powder for comparison, each having a mesh size of 80 or less, were obtained as shown in Table 1.
【表】【table】
【表】
つづいて、これらの合金鋼粉にステアリン酸亜
鉛1%と所定量の天然黒鉛粉、および、一部につ
いてはフエロりん粉(27wt.%P)を添加し、
6t/cm2の圧力で、幅10.0mm、長さ35.1mm,厚み6.5
mmの試験片を成形し、アンモニア分解ガス中600
℃で30分脱ろうしたのち、同一ガス中りんを添加
しないものは1200℃、添加したものは1150℃で、
それぞれ60分焼結した。
本発明による鋼粉および比較用鋼粉を使用した
場合の圧粉密度、焼結密度比、焼結体形状歪みお
よび炭化物平均粒度を第2表にまとめて示す。こ
こにおいて、焼結密度比は真密度に対する比で示
し、焼結体形状歪みは、同一の試験片の幅の測定
値に、測定位置によつて最大0.02mmを超える差が
ある場合に、歪みありと判定した。また、炭化物
平均粒度は焼結合金断面の600倍の光顕写真によ
つて観察される炭化物の平均粒度を、同面積をも
つ円の直径に換算して示したものである。[Table] Next, 1% zinc stearate, a predetermined amount of natural graphite powder, and some ferrophosphor powder (27wt.%P) were added to these alloy steel powders,
At a pressure of 6t/ cm2 , width 10.0mm, length 35.1mm, thickness 6.5
600 mm specimens were molded in ammonia decomposition gas.
After dewaxing at ℃ for 30 minutes, the temperature in the same gas was 1200℃ without phosphorus added, and 1150℃ with phosphorus added.
Each was sintered for 60 minutes. Table 2 summarizes the green powder density, sintered density ratio, sintered body shape distortion, and average carbide particle size when using the steel powder according to the present invention and the steel powder for comparison. Here, the sintered density ratio is expressed as the ratio to the true density, and the shape distortion of the sintered body is defined as the distortion when the measured width of the same specimen differs by a maximum of 0.02 mm depending on the measurement position. It was determined that there was. Further, the average grain size of carbides is the average grain size of carbides observed in a light micrograph of a sintered alloy cross section magnified 600 times, converted into the diameter of a circle having the same area.
【表】
本発明による鋼粉A,B,C,D,およびEを
使用した試験番号1〜6はいずれも圧粉密度
6g/cm3以上、焼結密度比95%以上と好ましい値
であり、焼結体形状歪みが無く、しかも炭化物粒
度が10μm以下の微細組織を有し、耐摩耗焼結合
金として優れた性質を備えている。
一方、試験番号7〜11はいずれも比較用の鋼粉
を使用したものである。試験番号7および8は、
それぞれ試験番号1および4にくらべて、それぞ
れCとNの含有量が本発明による範囲よりも高い
鋼粉(FおよびG)を使用しているため、圧粉密
度が低く、その結果、圧粉体強度が不十分なうえ
に、焼結中の収縮によつて95%以上の焼結密度比
を得ることができない。しかも、収縮が均一に進
行しないため、焼結体形状に歪みが出ている。
試験番号9〜11は、それぞれ試験番号4〜6に
くらべて、平均粒径が本発明による範囲よりも大
きい鋼粉(H,IおよびJ)を使用しているた
め、炭化物粒度がいずれも10μmを超えており、
焼結合金の耐衝撃性の観点から好ましくない。
第1図および第2図にそれぞれ試験番号6(本
発明鋼粉使用)および試験番号11(比較鋼粉使用)
の断面の光顕組織写真を比較して示す。マトリツ
クスはベイナイト(黒)およびマルテンサイト
(白)であり、炭化物(白)が試験番号6では細
かく点在して比較的球状であるのに対し、試験番
号11ではマトリツクスの結晶粒界に沿つて成長粗
大化しているのが見られる。
また、試験番号9および11にあつては、鋼粉の
粒度が粗いために圧粉体中に大きな空孔が存在
し、その結果、焼結中の収縮が不均一になりやす
く、焼結体形状歪みが大きい。さらに、Pを添加
した試験番号10では、これも鋼粉粒度が粗いため
にPの効果が発揮できず、本発明による鋼粉を用
いた試験番号5にくらべて焼結密度が低くなるこ
とは前述したとおりである。
上述したように、本発明によれば、噴霧鋼粉の
成分とともに粒度を所定範囲内に限定することに
よつて、本発明による焼結合金鋼粉を用いて高密
度で、形状歪みが小さく、微細細織を有する耐摩
耗焼結合金を製造し得るという効果が得られる。[Table] Test numbers 1 to 6 using steel powders A, B, C, D, and E according to the present invention all had green powder density.
It has a preferable value of 6 g/cm 3 or more and a sintered density ratio of 95% or more, has no shape distortion of the sintered body, and has a microstructure with a carbide grain size of 10 μm or less, and has excellent properties as a wear-resistant sintered alloy. We are prepared. On the other hand, test numbers 7 to 11 all used steel powder for comparison. Test numbers 7 and 8 are
Compared to test numbers 1 and 4, respectively, steel powders (F and G) with higher C and N contents than the range according to the present invention are used, so the green density is low, and as a result, the green powder In addition to insufficient body strength, it is not possible to obtain a sintered density ratio of 95% or more due to shrinkage during sintering. Moreover, since the shrinkage does not proceed uniformly, the shape of the sintered body is distorted. Test numbers 9 to 11 use steel powder (H, I, and J) whose average particle size is larger than the range according to the present invention compared to test numbers 4 to 6, so the carbide particle size is 10 μm in all cases. exceeds
This is not preferred from the viewpoint of impact resistance of the sintered alloy. Test number 6 (using the steel powder of the present invention) and test number 11 (using the comparative steel powder) are shown in Figures 1 and 2, respectively.
A comparison of light microscopic microstructure photographs of cross-sections is shown. The matrix is bainite (black) and martensite (white), and the carbides (white) are finely scattered and relatively spherical in test number 6, while in test number 11 they are found along the grain boundaries of the matrix. It can be seen that the growth is becoming coarser. In addition, in test numbers 9 and 11, large pores existed in the compact due to the coarse grain size of the steel powder, and as a result, shrinkage during sintering tended to be uneven, and the sintered compact Large shape distortion. Furthermore, in Test No. 10 in which P was added, the effect of P could not be exhibited because the steel powder grain size was coarse, and the sintered density was lower than in Test No. 5 in which steel powder according to the present invention was used. As mentioned above. As described above, according to the present invention, by limiting the components and particle size of the atomized steel powder within a predetermined range, the sintered alloy steel powder according to the present invention can be used to produce high density, low shape distortion, The effect is that a wear-resistant sintered alloy having a fine texture can be produced.
第1図は本発明鋼粉を使用した焼結合金の断面
の光顕組織写真(600倍)、第2図は、比較鋼粉を
使用した焼結合金の断面の光顕組織写真(600倍)
を示す。
Figure 1 is a light micrograph (600x) of a cross section of a sintered alloy using the steel powder of the present invention, and Figure 2 is a light micrograph (600x) of a cross section of a sintered alloy using comparative steel powder.
shows.
Claims (1)
下、N0.2%以下を含み、残部Feおよび2%以下
の不可避下純物からなり、ふるい分析による粒度
分布から求めた平均粒径が30〜50μmであること
を特徴とする耐摩耗焼結合金用鋼粉。 2 重量比でCr3〜20%,Si0.3〜2%,C0.3%以
下、N0.2%以下、NiおよびCuの1種または2種
を5%以下を含み残部Feおよび2%以下の不可
避不純物からなり、ふるい分析による粒度分布か
ら求めた平均粒径が30〜50μmであることを特徴
とする耐摩耗焼結合金用鋼粉。 3 重量比でCr3〜20%,Si0.3〜2%,C0.3%以
下、N0.2%以下、V,MoおよびWの1種または
2種以上を5%以下を含み、残部Feおよび2%
以下の不可避不純物からなり、ふるい分析による
粒度分布から求めた平均粒径が30〜50μmである
ことを特徴とする耐摩耗焼結合金用鋼粉。 4 重量比でCr3〜20%,Si0.3〜2%,C0.3%以
下、N0.2%以下、NiおよびCuの1種または2種
を5%以下、V,MoおよびWの1種または2種
以上を5%以下を含み、残部Feおよび2%以下
の不可避不純物からなり、ふるい分析による粒度
分布から求めた平均粒径が30〜50μmであること
を特徴とする耐摩耗焼結合金用鋼粉。[Scope of Claims] 1 Contains 3 to 20% Cr, 0.3 to 2% Si, 0.3% or less of C, and 0.2% or less of N, the balance being Fe and 2% or less of unavoidable impurities, A steel powder for wear-resistant sintered alloys, characterized in that the average particle size determined from the particle size distribution by sieve analysis is 30 to 50 μm. 2 Contains 3 to 20% Cr, 0.3 to 2% Si, 0.3% or less C, 0.2% or less N, 5% or less of one or both of Ni and Cu, the balance being Fe and 2% or less by weight. A steel powder for use in wear-resistant sintered alloys, which contains unavoidable impurities and has an average particle size of 30 to 50 μm as determined from particle size distribution by sieve analysis. 3 Contains 3 to 20% of Cr, 0.3 to 2% of Si, 0.3% or less of C, 0.2% or less of N, 5% or less of one or more of V, Mo, and W, and the balance is Fe and 2%
A steel powder for wear-resistant sintered alloys, comprising the following unavoidable impurities and having an average particle size of 30 to 50 μm as determined from particle size distribution by sieve analysis. 4 Weight ratio: Cr3-20%, Si0.3-2%, C0.3% or less, N0.2% or less, 5% or less of one or both of Ni and Cu, one of V, Mo and W Or a wear-resistant sintered alloy containing 5% or less of two or more types, the balance being Fe and 2% or less of unavoidable impurities, and having an average particle size of 30 to 50 μm as determined from the particle size distribution by sieve analysis. Steel powder for use.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57156392A JPS5947358A (en) | 1982-09-08 | 1982-09-08 | Steel powder for wear resistant sintered alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57156392A JPS5947358A (en) | 1982-09-08 | 1982-09-08 | Steel powder for wear resistant sintered alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5947358A JPS5947358A (en) | 1984-03-17 |
| JPS635441B2 true JPS635441B2 (en) | 1988-02-03 |
Family
ID=15626733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57156392A Granted JPS5947358A (en) | 1982-09-08 | 1982-09-08 | Steel powder for wear resistant sintered alloy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5947358A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008505248A (en) * | 2004-07-02 | 2008-02-21 | ホガナス アクチボラゲット | Stainless steel powder |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7473295B2 (en) | 2004-07-02 | 2009-01-06 | Höganäs Ab | Stainless steel powder |
| KR100846047B1 (en) * | 2004-07-02 | 2008-07-11 | 회가내스 아베 | Stainless steel powder |
| CA2700056C (en) * | 2007-09-28 | 2016-08-16 | Hoeganaes Ab (Publ) | Metallurgical powder composition and method of production |
-
1982
- 1982-09-08 JP JP57156392A patent/JPS5947358A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008505248A (en) * | 2004-07-02 | 2008-02-21 | ホガナス アクチボラゲット | Stainless steel powder |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5947358A (en) | 1984-03-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5481380B2 (en) | Metallurgical powder composition and production method | |
| KR20040066937A (en) | Sinterable metal powder mixture for the production of sintered components | |
| KR102350989B1 (en) | A method for producing a sintered component and a sintered component | |
| US6066191A (en) | Hard molybdenum alloy, wear resistant alloy and method for manufacturing the same | |
| US6468468B1 (en) | Method for preparation of sintered parts from an aluminum sinter mixture | |
| EP0499392B1 (en) | Method for producing a wear-resistant iron-based sintered alloy | |
| DE3224420C2 (en) | Process for the aftertreatment of a sintered sliding element | |
| SE541758C2 (en) | Iron-based alloy powder for powder metallurgy, and sinter-forged member | |
| JP2007046166A (en) | Use of mixture composed of iron based powder, graphite and solid lubricant particle | |
| JP4201830B2 (en) | Iron-based powder containing chromium, molybdenum and manganese and method for producing sintered body | |
| JPS6365051A (en) | Manufacture of ferrous sintered alloy member excellent in wear resistance | |
| JP3446322B2 (en) | Alloy steel powder for powder metallurgy | |
| JPH04325648A (en) | Method for producing aluminum sintered alloy | |
| KR20200128158A (en) | Alloy steel powder for powder metallurgy and iron-based mixed powder for powder metallurgy | |
| JPS635441B2 (en) | ||
| JP4051167B2 (en) | Wear-resistant iron-based sintered alloy | |
| EP0516404A1 (en) | Mixed powder for powder metallurgy and sintered product thereof | |
| JP2002047502A (en) | Cr-containing Fe-based alloy powder and Cr-containing Fe-based alloy sintered body using the same | |
| WO2019111833A1 (en) | Steel alloy powder | |
| CN114728331B (en) | Alloy steel powder for powder metallurgy, iron-based mixed powder and sintered body for powder metallurgy | |
| WO2019111834A1 (en) | Partial diffusion alloyed steel powder | |
| JP2001073100A (en) | Fe-based sintered body, powder for producing Fe-based sintered body, and method for producing Fe-based sintered body | |
| JPH0751721B2 (en) | Low alloy iron powder for sintering | |
| EP0099067B1 (en) | Wear-resistant sintered ferrous alloy and method of producing same | |
| JPH0159321B2 (en) |