JPH0140081B2 - - Google Patents
Info
- Publication number
- JPH0140081B2 JPH0140081B2 JP54055181A JP5518179A JPH0140081B2 JP H0140081 B2 JPH0140081 B2 JP H0140081B2 JP 54055181 A JP54055181 A JP 54055181A JP 5518179 A JP5518179 A JP 5518179A JP H0140081 B2 JPH0140081 B2 JP H0140081B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- mixture
- iron
- copper
- iron 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 46
- 239000000843 powder Substances 0.000 claims description 45
- 239000000203 mixture Substances 0.000 claims description 39
- 239000010949 copper Substances 0.000 claims description 29
- 229910052802 copper Inorganic materials 0.000 claims description 26
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 20
- 229910052698 phosphorus Inorganic materials 0.000 claims description 15
- 238000009792 diffusion process Methods 0.000 claims description 13
- 229910052742 iron Inorganic materials 0.000 claims description 13
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 11
- 239000011574 phosphorus Substances 0.000 claims description 11
- 239000000956 alloy Substances 0.000 claims description 10
- 229910045601 alloy Inorganic materials 0.000 claims description 10
- 238000005275 alloying Methods 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000004663 powder metallurgy Methods 0.000 claims description 4
- 239000002245 particle Substances 0.000 description 20
- 239000002184 metal Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 9
- 238000005191 phase separation Methods 0.000 description 6
- 238000005245 sintering Methods 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000005056 compaction Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 238000009826 distribution Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000005749 Copper compound Substances 0.000 description 2
- 150000001880 copper compounds Chemical class 0.000 description 2
- IYRDVAUFQZOLSB-UHFFFAOYSA-N copper iron Chemical compound [Fe].[Cu] IYRDVAUFQZOLSB-UHFFFAOYSA-N 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- DPTATFGPDCLUTF-UHFFFAOYSA-N phosphanylidyneiron Chemical compound [Fe]#P DPTATFGPDCLUTF-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 229910052774 Proactinium Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000754 repressing effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0207—Using a mixture of prealloyed powders or a master alloy
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
Description
本発明は粉末冶金による精密部品の製造に用い
られる鉄系合金粉末の製造法に関するものであ
る。本発明によつて得られる粉末は寸法正確性お
よび機械強度が強く要求される精密部品の製造を
容易ならしめるものである。製造工程は鉄粉混合
物を最終部品の形状に近似する粗成型体に圧縮す
る−圧縮作業を容易にするための潤滑剤と混合す
ることによつて始まる。この粗成型体は次いで成
分が強度、可鍛性等において最終製品としての特
徴と有する温度にまで焼成される。この方法で得
られる部品よりも正確な寸法の部品を得ることが
屡々要求されるが、これは再度の圧縮工程、すな
わちキヤリブレーシヨンによつて行なわれ、それ
によつて部品は極度に正確な寸法となる。屡々要
求される高強度の粉末冶金による部品を得るため
には合金化粉末が出発原料として用いられ、これ
には実質的に二つの種類、すなわち金属成分粉末
混合物と所謂噴霧合金粉末とが用いられる。
金属成分粉末混合物は合金化元素を元素状また
は焼成中に鉄粉中で分解し得る化合物として鉄粉
と混合したものであり、一方所謂噴霧合金粉末は
希望する合金成分を含有した溶鋼を噴霧すること
によつてつくられる。
金属成分粉末混合物の欠点の一つは相分離の危
険性であり、この危険性は相互に異なつた特性の
粉末、例えば異なつた粒径のものが機械的に結合
されることなく混合されるという事実によつて生
ずる。この相分離は金属成分粉末混合物から製造
される粗成型品の組成が変動するという結果を生
じ、これはさらに焼成時における寸法変化をもた
らすことになる。金属成分粉末混合物のもう一つ
の欠点は特に合金化元素が小粒径である場合の粉
塵化傾向である。このことは困難な環境問題をも
たらすこととなる。
一方、噴霧合金粉末はそれぞれの粉末粒子が目
的とする合金組成であるために相分離の危険性は
完全に消失する。また飛散の危険性も小粒径の合
金成分がないために減少する。然しながら、予め
合金化された噴霧合金粉末は別の大きな欠点を有
する。すなわち圧縮性の悪さがこれであり、これ
は合金化成分の粒子粉末上に有する無溶媒焼鈍効
果によるものである。高い強度の必須条件である
高密度を得るためにすぐれた圧縮性は不可欠のも
のである。これと反対に、金属成分粉末混合物の
圧縮性はその中に含まれる鉄粉末の圧縮性と実質
的に同一である。この事実は金属成分粉末粒子を
特徴づける合金組成の柔軟性とともに金属成分粉
末粒子を合金用粉末として最も広く使用されるも
のとした。
鉄を基礎成分とする焼結部品の製造においては
強度を増加するために合金化元素として銅を使用
することが長い間知られている。また鉄−銅−混
合物からつくられた部品が焼結の際に成長または
膨潤に付されることもすでに知られている。部品
を長期間にわたつて製造する場合、この成長また
は膨潤が望ましくない状態で部品間で変動する
が、この変動は主として金属成分粉末混合物の上
述の相分離の危険性にもとづくものである。
鉄系粉末に関する特願昭52−131628号(特開昭
53−92306号)の発明は、高圧縮度の長所と相分
離および粉塵化の危険性の減少とを組み合わせた
もので、この粉末は製品の寸法安定性が極めて優
れていることも知られ、全く予想外に、ある分野
ではキヤリブレーシヨン作業が不要となることも
知られているものである。特願昭52−131628号の
拡散合金鉄粉の製造は次のようにして行なわれ
る。すなわち、350μmよりも小さい、好ましく
は175μmよりも小さく、最も好ましくは150μm
よりも小さい粒径の鉄粉が、175μmよりも小さ
い、好ましくは75μmよりも小さい粒径の銅また
は易還元性銅化合物の粉末と混合される。次いで
この粉末混合物は還元雰囲気中で700〜950℃、好
ましくは750〜850℃で15分〜10時間、好ましくは
0.5〜5時間熱処理される。これによつて、拡散
による圧縮度の低下が0.15g/cm3(ASTM基準
B331−64)よりも大きい程度にまで銅の拡散を
もたらすことなしに、鉄粒子に銅を焼結させるも
のである。熱処理は粉末の全酸素含量が1.2%よ
りも少ない、好ましくは0.8%よりも少なくなる
ように行なわれる。こうしてつくられたケーキは
最大粒径350μm未満、好ましくは175μm未満、
最も好ましくは150μm未満に粉砕される。こう
して得られる粉末が、以下に拡散合金鉄と呼ばれ
るものである。
銅との拡散合金鉄粉は、さらに希望の銅含量の
混合物にするために純鉄粉と混合される。こうし
て得られた粉末を粉末冶金に用いる場合には鉄粉
の他に0〜2%、好ましくは0〜1%のグラフア
イト、0〜2%、好ましくは0〜1%の粉末固体
潤滑剤を添加することが望ましい。拡散焼鈍され
る初期混合物では好ましい銅含量は1〜20%、好
ましくは5〜15%、最も好ましくは8〜12%であ
り、一方最終混合物の銅含量は1〜5%である。
基礎粉末として用いる鉄粉は効率のよい付着の
ために大きい比表面を有することが必要である。
従つてスポンジ鉄からつくられる鉄粉、所謂スポ
ンジ粉が特願昭52−131628号の発明の粉末を製造
する場合に望ましい。この特願昭52−131628号の
発明の粉末は燐と合金化することにより、寸法安
定性を一層改善することが可能であることが知ら
れた。一定量の燐を含有させることによつて混合
粉末を単に焼結するだけで加熱時に燐が拡散して
合金化が達成されるものであり、この場合に得ら
れる効果、特に燐含量が0.15〜1.0重量%の範囲
内にある時の驚くべき効果は寸法変化の絶対値の
減少と同様にこの絶縁値の分布の減少である。こ
のように本発明の粉末は寸法正確性と高強度を有
する精密部品の製造において実質的にキヤリブレ
ーシヨンを不要にするものである。
本発明は合金化粉末の製造は次のようにして行
なわれる。すなわち、最大粒径350μm未満の鉄
粉と1〜20%の最大粒径の175μm未満の銅また
は還元性銅化合物の粉末との混合物がつくられ、
この混合物が還元雰囲気中で700〜950℃の温度
で、15分〜10時間、好ましくは0.5〜5時間焼鈍
処理され、かくして得られたケーキが最大粒径
350μm未満の粉末に粉砕され、焼鈍が焼鈍粉末
の圧縮度がASTM基準B331−64で最大限、相当
する鉄−銅粉混合物の圧縮度よりも小さい0.15
g/cm3で全酸素含量が1.2%以下となるような温
度および時間で行なわれ、さらにかくして得られ
た銅合金化鉄粉末を純鉄粉と混合して希望する銅
含量の混合物とし、次いで燐を燐鉄の形で希望す
る燐合量まで添加する。燐含量は1.5重量%まで、
好ましくは0.15〜1.0%である。なお、燐分は0.15
%未満では本願の望ましい効果がなく、また燐分
1.0%を越えると相分離の危険性が急激に増大し、
その結果製品の破壊の危険性が増大する。以下に
本発明の実施例を示す。
実施例 1
H、IおよびKの下記組成の三種類の混合物が
つくられた。
混合物H:94.2% 最大粒径147μmのスポンジ
鉄粉
5.0% 最大粒径147μmのスポンジ
銅粉
0.8% ステアリン酸亜鉛粉
混合物I:49.2% 最大粒径147μmのスポンジ
鉄粉
50.0% 銅含量10.0%、最大粒径147μ
mの拡散合金鉄粉
0.8% ステアリン酸亜鉛粉
混合物K:46.2% 最大粒径147μmのスポンジ
鉄粉
50.0% 銅含量10.0%、最大粒径147μ
mの拡散合金鉄粉
3.0% 燐含量15%、最大粒径44μm
の燐鉄
0.8% ステアリン酸亜鉛粉
それぞれの混合物からドルスト装自動プレスで
10×10×30mmの長方形の試験片2500ケがつくられ
た。次いで部品はendorgeneガス雰囲気中で1120
℃で30分間炉で焼成された。焼結後、統計的に充
分な量の部品を取り出してそれぞれの寸法安定性
を測定した。混合物Hでは全体分布値42μm、混
合物Iでは22μm、混合物Kでは12μmであつた。
このように寸法変化の分布はH、IよりもKが実
質的に少なかつた。
このことは寸法安定性に関しての予めきめられ
た要求、すなわち予めきめられた許容範囲が材料
Kを使用することによつて容易に達成し得ること
を意味している。上の実施例での材料で得られた
寸法正確度は許容誤差範囲IT6級に相当し、一
方、材料HはIT9、材料IはIT7であつた。許容
誤差範囲IT6に相当する寸法正確度を有する部品
は充分にキヤリブレーシヨンされたものよりも優
れ、これは焼結後再プレスして到達する許容誤差
範囲である。
実施例 2
Na、b;Oa、b;Pa、bの下記組成の6種類
の合金化粉末混合物がつくられた。
混合物Na:93.75% Fe
5.0 % Cu(Cu粉)
0.45% P
0.8 % Znステアレート
混合物Oa:93.65% Fe
5.0 % Cu(Cu粉)
0.45% P
0.4 % C
0.5 % Znステアレート
混合物Pa:94.10% Fe
5.0 % Cu(Cu粉)
4.0 % C
0.5 % Znステアレート
混合物Nb:93.75% Fe
5.0 % Cu(10%Cu含有拡散合金
化鉄粉)
0.45% P
0.8 % Znステアレート
混合物Ob:93.65% Fe
5.0 % Cu(10%Cu含有拡散合金
化鉄粉)
0.45% P
0.4 % C
0.5 % Znステアレート
混合物Pb:94.10% Fe
5.0 % Cu(10%Cu含有拡散合金
化鉄粉)
0.4 % C
0.5 % Znステアレート
これら6種類の混合物から590MPaの圧力で試
験片がプレスされ、適当な炭素値のendorgenous
雰囲気中で1120℃、30分焼結された。測定された
試験片の機械的特性は下表の通りであつた。
The present invention relates to a method for producing iron-based alloy powder used in the production of precision parts by powder metallurgy. The powder obtained according to the present invention facilitates the manufacture of precision parts that require strong dimensional accuracy and mechanical strength. The manufacturing process begins by compacting the iron powder mixture into a rough compact approximating the shape of the final part - mixing it with a lubricant to facilitate the compaction operation. This compact is then fired to a temperature at which the components have the characteristics of the final product in terms of strength, malleability, etc. It is often necessary to obtain parts with more precise dimensions than those obtained with this method, and this is accomplished by a second compression step, or calibration, whereby the parts are produced with extremely precise dimensions. becomes. In order to obtain the often required high-strength powder metallurgy components, alloyed powders are used as starting materials, of which essentially two types are used: metal component powder mixtures and so-called spray alloyed powders. . Metal component powder mixtures are alloying elements mixed with iron powder either in elemental form or as compounds that can be decomposed in the iron powder during firing, while so-called spray alloy powders are made by spraying molten steel containing the desired alloying components. created by One of the disadvantages of metal component powder mixtures is the risk of phase separation, which occurs when powders with mutually different properties, e.g. of different particle sizes, are mixed without being mechanically bonded. arises from facts. This phase separation results in a compositional variation of the molded article produced from the metal component powder mixture, which in turn leads to dimensional changes during firing. Another disadvantage of metal component powder mixtures is their tendency to dust, especially when the alloying elements are of small particle size. This poses difficult environmental problems. On the other hand, since each powder particle of the sprayed alloy powder has the intended alloy composition, the risk of phase separation is completely eliminated. The risk of splashing is also reduced due to the absence of small particle size alloying components. However, prealloyed atomized alloy powders have another major disadvantage. That is, the compressibility is poor, and this is due to the solvent-free annealing effect on the particle powder of the alloying component. Excellent compressibility is essential to obtain high density, which is a prerequisite for high strength. In contrast, the compressibility of the metal component powder mixture is substantially the same as that of the iron powder contained therein. This fact, along with the flexibility of alloy composition that characterizes metal component powder particles, has made metal component powder particles most widely used as alloying powders. It has long been known to use copper as an alloying element in order to increase the strength in the production of sintered parts based on iron. It is also already known that parts made from iron-copper mixtures are subjected to growth or swelling during sintering. When parts are produced over long periods of time, this growth or swelling undesirably varies from part to part, and this variation is primarily due to the above-mentioned risk of phase separation of the metal component powder mixture. Japanese Patent Application No. 52-131628 concerning iron-based powder
The invention of No. 53-92306) combines the advantages of a high degree of compaction with a reduced risk of phase separation and dusting, and the powder is also known to have excellent dimensional stability of the product. Quite unexpectedly, it has also been found that calibration operations are no longer necessary in certain areas. The diffusion alloyed iron powder of Japanese Patent Application No. 52-131628 is manufactured as follows. i.e. smaller than 350 μm, preferably smaller than 175 μm, most preferably 150 μm
is mixed with copper or easily reducible copper compound powder having a particle size of less than 175 μm, preferably less than 75 μm. This powder mixture is then heated in a reducing atmosphere at 700-950°C, preferably 750-850°C for 15 minutes to 10 hours, preferably
Heat treated for 0.5-5 hours. This reduces the degree of compaction due to diffusion by 0.15 g/cm 3 (ASTM standard
B331-64) sintering copper into iron particles without causing diffusion of copper to a greater extent than B331-64). The heat treatment is carried out such that the total oxygen content of the powder is less than 1.2%, preferably less than 0.8%. The cake thus produced has a maximum particle size of less than 350 μm, preferably less than 175 μm,
Most preferably it is ground to less than 150 μm. The powder thus obtained is hereinafter referred to as diffusion alloy iron. Diffusion alloyed iron powder with copper is further mixed with pure iron powder to obtain a mixture with the desired copper content. When the powder thus obtained is used in powder metallurgy, 0 to 2%, preferably 0 to 1% of graphite, and 0 to 2%, preferably 0 to 1% of a powder solid lubricant are added in addition to the iron powder. It is desirable to add. The preferred copper content in the initial mixture to be diffusion annealed is 1-20%, preferably 5-15%, most preferably 8-12%, while the final mixture has a copper content of 1-5%. The iron powder used as the base powder needs to have a large specific surface for efficient adhesion.
Therefore, iron powder made from sponge iron, so-called sponge powder, is desirable for producing the powder of the invention of Japanese Patent Application No. 131,628/1982. It has been found that the dimensional stability of the powder of the invention disclosed in Japanese Patent Application No. 131,628/1988 can be further improved by alloying it with phosphorus. By simply sintering the mixed powder by containing a certain amount of phosphorus, the phosphorus diffuses during heating and alloying is achieved. A surprising effect within the 1.0 weight percent range is a reduction in the distribution of this insulation value as well as a reduction in the absolute value of the dimensional change. Thus, the powder of the present invention substantially eliminates the need for calibration in the manufacture of precision parts with dimensional accuracy and high strength. In the present invention, the alloyed powder is manufactured as follows. That is, a mixture of iron powder with a maximum particle size of less than 350 μm and 1 to 20% of copper or reducible copper compound powder with a maximum particle size of less than 175 μm is made,
This mixture is annealed at a temperature of 700 to 950°C in a reducing atmosphere for 15 minutes to 10 hours, preferably 0.5 to 5 hours, and the cake thus obtained has a maximum particle size.
The degree of compaction of the annealed powder is the maximum according to ASTM standard B331-64, which is 0.15 less than the degree of compaction of the corresponding iron-copper powder mixture.
The copper alloyed iron powder thus obtained is mixed with pure iron powder to form a mixture with the desired copper content, and then Add phosphorus in the form of iron phosphorus to the desired phosphorus content. Phosphorus content up to 1.5% by weight,
Preferably it is 0.15-1.0%. In addition, the phosphorus content is 0.15
If the phosphorus content is less than %, the desired effect of the present application will not be obtained, and
If it exceeds 1.0%, the risk of phase separation increases rapidly;
As a result, the risk of product destruction increases. Examples of the present invention are shown below. Example 1 Three mixtures of H, I and K were made with the following compositions. Mixture H: 94.2% Sponge iron powder with a maximum particle size of 147 μm 5.0% Sponge copper powder with a maximum particle size of 147 μm 0.8% Zinc stearate powder mixture I: 49.2% Sponge iron powder with a maximum particle size of 147 μm 50.0% Copper content 10.0%, max. Particle size 147μ
m diffusion alloy iron powder 0.8% Zinc stearate powder mixture K: 46.2% Sponge iron powder 50.0% with maximum particle size 147μm Copper content 10.0%, maximum particle size 147μm
m diffusion alloy iron powder 3.0% phosphorus content 15%, maximum particle size 44μm
Iron phosphorus 0.8% and zinc stearate powder from each mixture in an automatic Dorst press.
2500 rectangular specimens measuring 10 x 10 x 30 mm were made. The parts are then heated for 1120 min in an endorgene gas atmosphere.
It was baked in a furnace for 30 minutes at °C. After sintering, a statistically sufficient number of parts were removed to measure their dimensional stability. The overall distribution value was 42 μm for mixture H, 22 μm for mixture I, and 12 μm for mixture K.
As described above, the distribution of dimensional changes was substantially smaller for K than for H and I. This means that the predetermined requirements regarding dimensional stability, ie the predetermined tolerance ranges, can be easily achieved by using material K. The dimensional accuracy obtained with the materials in the above examples corresponds to a tolerance range of IT6 class, while material H was IT9 and material I was IT7. A part with a dimensional accuracy corresponding to the tolerance range IT6 is better than a fully calibrated one, which is the tolerance range reached by repressing after sintering. Example 2 Six types of alloyed powder mixtures were made with the following compositions: Na, b; Oa, b; Pa, b. Mixture Na: 93.75% Fe 5.0% Cu (Cu powder) 0.45% P 0.8% Zn stearate mixture Oa: 93.65% Fe 5.0% Cu (Cu powder) 0.45% P 0.4% C 0.5% Zn stearate mixture Pa: 94.10% Fe 5.0% Cu (Cu powder) 4.0% C 0.5% Zn stearate mixture Nb: 93.75% Fe 5.0% Cu (diffusion alloyed iron powder containing 10% Cu) 0.45% P 0.8% Zn stearate mixture Ob: 93.65% Fe 5.0% Cu (diffusion alloyed iron powder containing 10% Cu) 0.45% P 0.4% C 0.5% Zn stearate mixture Pb: 94.10% Fe 5.0% Cu (diffusion alloyed iron powder containing 10% Cu) 0.4% C 0.5% Zn stearate A test piece was pressed from a mixture of these six types at a pressure of 590 MPa, and an endogenous
Sintered in an atmosphere at 1120℃ for 30 minutes. The measured mechanical properties of the test pieces were as shown in the table below.
【表】【table】
【表】
この結果から、銅粉末を鉄粉と混合して得られ
る強度は、銅粉末を銅で拡散合金化された鉄粉で
おきかえても影響のないことが知られる。銅で拡
散合金化された鉄粉からつくられた部品は特にそ
れが炭素および燐と合金化された時に優れた強度
を有し、一方これまでに得られた許容寸法範囲は
焼結後の工程だけで到達し得るものであつた。[Table] From this result, it is known that the strength obtained by mixing copper powder with iron powder is not affected even if the copper powder is replaced with iron powder diffusion alloyed with copper. Components made from copper-diffusion-alloyed iron powder have excellent strength, especially when it is alloyed with carbon and phosphorus, while the tolerance ranges achieved so far are limited by post-sintering processes. It was something that could have been achieved alone.
Claims (1)
合物の銅含量が希望する銅含量となるような量の
純鉄粉末を混合し、かつ合金化成分としてさらに
0.15〜1.0重量%の燐分を含有させることを特徴
とする良好な寸法正確性と高強度を有する粉末冶
金による精密部品製造用鉄系合金粉末の製造法。1. Mix the iron powder diffusion alloyed with copper with pure iron powder in an amount such that the copper content of the resulting mixture becomes the desired copper content, and further add as an alloying component.
A method for producing iron-based alloy powder for manufacturing precision parts by powder metallurgy, which has good dimensional accuracy and high strength, and is characterized by containing 0.15 to 1.0% by weight of phosphorus.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE7805205A SE414191B (en) | 1978-05-03 | 1978-05-03 | LIKE TO LIKE THE PATENT 7612217-5 MAKE IRON-BASED POWDER |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS552791A JPS552791A (en) | 1980-01-10 |
| JPH0140081B2 true JPH0140081B2 (en) | 1989-08-25 |
Family
ID=20334855
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5518179A Granted JPS552791A (en) | 1978-05-03 | 1979-05-04 | Manufacture of powder for powder metallurgy |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS552791A (en) |
| DE (1) | DE2917882C2 (en) |
| ES (1) | ES8100771A2 (en) |
| FR (1) | FR2424967A2 (en) |
| GB (1) | GB2023184B (en) |
| SE (1) | SE414191B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK0420962T3 (en) * | 1989-04-07 | 1994-04-25 | Electrolux Ab | Process for making dimensionally accurate pieces |
| PL232405B1 (en) * | 2015-07-27 | 2019-06-28 | Akademia Gorniczo Hutnicza Im Stanislawa Staszica W Krakowie | Easily sintered iron based alloy powder, method of producing it and application, and the sintered product |
| KR102210213B1 (en) * | 2017-10-30 | 2021-01-29 | 티피알 가부시키가이샤 | Iron-based sintered alloy valve guide and its manufacturing method |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB538227A (en) * | 1939-12-12 | 1941-07-25 | William Arthur Oubridge | Improvements in or relating to the manufacture of metal articles or masses |
| US3752712A (en) * | 1971-06-07 | 1973-08-14 | Domtar Ltd | Iron copper prealloys |
| GB1449809A (en) * | 1972-11-27 | 1976-09-15 | Fischmeister H | Forging of metal powders |
| SE393635B (en) * | 1976-06-24 | 1977-05-16 | Hoeganaes Ab | PHOSPHORIC STABLE POWDER AND KIT FOR ITS PREPARATION |
-
1978
- 1978-05-03 SE SE7805205A patent/SE414191B/en not_active IP Right Cessation
-
1979
- 1979-05-02 ES ES480145A patent/ES8100771A2/en not_active Expired
- 1979-05-02 FR FR7911086A patent/FR2424967A2/en active Granted
- 1979-05-03 DE DE19792917882 patent/DE2917882C2/en not_active Expired
- 1979-05-03 GB GB7915362A patent/GB2023184B/en not_active Expired
- 1979-05-04 JP JP5518179A patent/JPS552791A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| ES480145A0 (en) | 1980-11-01 |
| FR2424967A2 (en) | 1979-11-30 |
| FR2424967B2 (en) | 1984-05-11 |
| DE2917882A1 (en) | 1979-11-15 |
| GB2023184B (en) | 1982-10-06 |
| GB2023184A (en) | 1979-12-28 |
| SE414191B (en) | 1980-07-14 |
| JPS552791A (en) | 1980-01-10 |
| ES8100771A2 (en) | 1980-11-01 |
| DE2917882C2 (en) | 1987-01-08 |
| SE7805205L (en) | 1979-11-04 |
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