JPH02111802A - Manufacture of green compact by using powder having super plastic function - Google Patents

Manufacture of green compact by using powder having super plastic function

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Publication number
JPH02111802A
JPH02111802A JP26159788A JP26159788A JPH02111802A JP H02111802 A JPH02111802 A JP H02111802A JP 26159788 A JP26159788 A JP 26159788A JP 26159788 A JP26159788 A JP 26159788A JP H02111802 A JPH02111802 A JP H02111802A
Authority
JP
Japan
Prior art keywords
powder
superplastic
molded body
compression molding
function
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.)
Pending
Application number
JP26159788A
Other languages
Japanese (ja)
Inventor
Takuichi Imanaka
拓一 今中
Yasuhiro Kakio
垣生 泰弘
Toshihiko Emi
江見 俊彦
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.)
JFE Steel Corp
Original Assignee
Kawasaki Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP26159788A priority Critical patent/JPH02111802A/en
Publication of JPH02111802A publication Critical patent/JPH02111802A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To manufacture a precise green compact having high density by giving super plastic function in powder manufactured with water atomizing method and compacting this powder with a super plastic compacting mold. CONSTITUTION:Components of base alloy powder are designed so as to obtain the composition showing high strength and high toughness and this powder is manufactured, for example with the water atomizing method. For example, Fe-Cu alloy powder having the super plastic function is mixed with this base alloy powder and compacted in the super plastic expressing range of the Fe-Cu alloy. Then, as the temp. of condition of the super plastic deformation is low, the condition of the base alloy powder, in which the components are designed to the aimed strength and toughness and the structure is controlled, can be held as it is and the precise green compact is obtd. at high density.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、超塑性機能を有する粉末を用いて高密度で精
密な成型焼結部品を製造する技術に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a technology for manufacturing high-density, precise molded sintered parts using powder having superplastic functionality.

[従来の技術] 粉末冶金技術は、その特長として、塊状固体材料を用い
た場合に比べ、 ■ 素材の加工歩出りが向上し、機械加工に要するコス
トが大幅に低減されること、 ■ 複雑な形状の機械部品の近似形状成型が可能である
こと、 ■ 高融点金属の成型に特に有利であること、などの利
点が挙げられる。
[Conventional technology] Powder metallurgy technology has the following characteristics compared to the case of using bulk solid materials: ■ It improves the machining yield of the material and significantly reduces the cost required for machining; ■ It is less complex. It has the following advantages: 1. It is particularly advantageous for molding high-melting point metals.

焼結部品の強度、特に靭性に関しては密度(相対密度)
が最も効果の大きいパラメータである。
Regarding the strength of sintered parts, especially toughness, density (relative density)
is the most effective parameter.

従って、焼結部品を考える場合、先ず、如何にして高い
相対密度を有した成型体を低重な工程で製造するかとい
うことが技術的な課題になる。
Therefore, when considering sintered parts, the first technical issue is how to manufacture a molded body with a high relative density in a light process.

高い相対密度を得る方法として、従来、相互拡散を利用
した高温焼結法、液相焼結法(1iquidphase
 sintering ) 、活性化焼結法(acti
vatedsinteringl 、高諷鍜造法または
HIP法がある。
Conventionally, methods for obtaining high relative density include high-temperature sintering using interdiffusion and liquid phase sintering.
sintering), activated sintering method (acti
There is a vated interring method, a high interpolation method, or a HIP method.

このうち、焼結法は、鋼粉の場合はl 000°C以上
の高温で成型体を処理するため (1)粒成長が起こること、 (2)折角の個々のアトマイズド扮の有している優れた
微細組織が破壊されてしまうこと。
Among these methods, the sintering method processes the molded product at a high temperature of over 1,000°C in the case of steel powder, so (1) grain growth occurs; (2) individual atomized products have The excellent microstructure is destroyed.

(3)高温焼結法では微細組織制御に難がある4=と、 (4)高温での処理のための成型品の寸法制御にも制約
があること、 等多くの問題が内在している。
(3) There are many problems inherent in high-temperature sintering, such as difficulty in controlling the microstructure (4) and (4) limitations in controlling the dimensions of molded products for high-temperature processing. .

一方、高温鍜造法またはHI P法は高密度成型体を得
るには優れた方法であるが、11考は金型にかかるコス
トが高く、後者は高圧ガス雰囲気下での成型ということ
からランニングコストが高い。
On the other hand, the high-temperature forging method or the HIP method is an excellent method for obtaining a high-density molded product, but the cost of the mold is high, and the latter requires high-pressure gas atmosphere, making it difficult to run. High cost.

また、高温ということで高2品焼結と同様の問題もある
Furthermore, due to the high temperature, there is a problem similar to high-temperature two-component sintering.

[発明が解決しようとする課題] 粉末の高温における圧縮成型過程は1III81/?の
粉末拉fの°塑性度yTaによって起ると考えられる。
[Problem to be solved by the invention] The compression molding process of powder at high temperature is 1III81/? This is thought to be caused by the degree of plasticity yTa of the powder f.

一般に、塑性f形によって加工硬化する現象は、変J[
aに伴って結晶内部に形成された転位間の相n作用によ
り転位の運動抵抗が増加する結束と1−て+F−17る
ものである。粉末の圧縮成型に対する変形抵抗も転位の
運動抵抗で決まる。
In general, the phenomenon of work hardening due to plastic f-shape is caused by the change J[
This is 1-+F-17 as a cohesion in which the motion resistance of the dislocations increases due to the phase n action between the dislocations formed inside the crystal as a result of a. The deformation resistance of powder to compression molding is also determined by the resistance to motion of dislocations.

高l晶変形の特殊なケースとして、tfl塑性変形があ
る。超□□□性は材料が等軸な微細結晶粒組織をイアす
る場合、ζ品度に対して安定な第2F+1(析出物。
A special case of high l-crystalline deformation is Tfl plastic deformation. Super □□□ properties are 2F+1 (precipitates) that are stable with respect to ζ grade when the material has an equiaxed fine grain structure.

α、γ2柑共存の場合の一方の相など)が共仔する場合
にその甘辛−1に固有の温度(比較的低温度)と変形速
度においで低応力下で異常延性を示す現象である。
This is a phenomenon in which abnormal ductility occurs under low stress at the temperature (relatively low temperature) and deformation rate specific to Amazara-1 when two phases (such as one phase when α and γ2 coexist) coexist.

今までに超塑性現象を示す材料はi?l多く見出されて
いるが、鉄鋼材料については、熱衝撃やクノーブなどの
高温強度の面で超・r性に起因する異常な大変形が機械
や構造物等の設計前に嫌われ従って鉄鋼材料としては5
′4常延姓の防止や、強度低下に如何に対処するかとい
う方向で、超塑性現象を捉えていたせいもあって、特に
微細結晶粒超塑性合金としての鉄鋼材料は少なく、実用
段階に入っているものはない。ましてや、粉末自体の超
・塑性特性を利用した技術は皆無であり、かつ粉末自体
の結晶粒超塑性挙動を直接的に証明した報告はない。
Is there any material that has shown superplasticity so far? However, in the case of steel materials, abnormal large deformations due to ultra-r properties such as thermal shock and Knob are avoided before designing machines and structures, and therefore steel materials are As for the material, 5
'4 Partly because the superplastic phenomenon was understood from the perspective of how to prevent Tsunenobu's problems and how to deal with strength loss, there were few steel materials in the form of fine-grained superplastic alloys, and it was not possible to put them into practical use. There's nothing inside. Furthermore, there is no technology that utilizes the superplastic properties of the powder itself, and there are no reports that directly prove the superplastic behavior of the crystal grains of the powder itself.

本発明はこの超塑性現象を応用した新規な粉末成型技術
を提供することを目的とするものである。
The object of the present invention is to provide a new powder molding technology that applies this superplastic phenomenon.

[課題を解決するための手段1 本発明は超塑性を応用した粉末冶金法であって1次の手
段をとる。
[Means for Solving the Problems 1] The present invention is a powder metallurgy method that applies superplasticity, and takes a first-order method.

(a)  超塑性機能を有する粉末を用いて成型体をM
1中性圧縮成型する。
(a) Making a molded body using powder with superplastic function
1 Neutral compression molding.

(b)  水アトマイズ法等により製造した粉末に、後
処理を施して超塑性機能を付与し、該粉末を用いて成型
体を超塑性圧縮成型によって製造する。
(b) Powder produced by a water atomization method or the like is post-treated to impart superplastic functionality, and a molded body is produced using the powder by superplastic compression molding.

(cl  超塑性機能を有するH扮に金属炭化物、金属
窒化物等の微細粉末やまたはァインセラミックス微粉末
を混合添加し、5扮の超塑性による濡れ性および超塑性
流動を応用して、成型体を圧縮成型する。
(cl) Fine powders such as metal carbides, metal nitrides, or fine ceramic powders are mixed and added to the H material which has a superplastic function, and molded by applying the wettability and superplastic flow of the five materials. Compression mold the body.

(d)  高強度、高靭性に成分設計した合金粉末を製
造し、該合金粉末に超塑性機能を有する粉末を添加混合
し、該添加した粉末の超塑性発現領域で圧縮成型加工す
る。
(d) An alloy powder whose components are designed to have high strength and high toughness is produced, a powder having a superplastic function is added and mixed with the alloy powder, and the added powder is compression molded in the superplastic expression region.

(e)  鉄粉または高強度、高靭性を示す塑性に成分
設計した合金銅粉をは扮とし、鉄基合金以外の超塑性粉
末を結合剤として用いて圧縮成型する。
(e) Compression molding is performed using iron powder or alloyed copper powder whose composition is designed to have high strength and high toughness and plasticity as a binder, using superplastic powder other than iron-based alloy as a binder.

(f)  また上記(d)または(e)の成型加工後に
拡散焼鈍工程を付加する。
(f) Further, a diffusion annealing process is added after the molding process in (d) or (e) above.

(g)  粉末の緻密化率ρが式 においで、Dがその粉末の粒界自己拡散係数に近い値を
有し、かつn=0.35〜1.0の値を示す粉末を用い
て成型体を圧縮成型する。
(g) Molding using a powder in which the densification rate ρ of the powder is in the formula, D has a value close to the grain boundary self-diffusion coefficient of the powder, and n = 0.35 to 1.0. Compression mold the body.

ただし、 ρ:粉末の緻密化率 ε:圧縮成型中の歪速度 に2:物質常数 ρ:相対密度 P^:付加応力 Eニャレグ率 [作用] 本発明は、粉末の超塑性挙動の実証または新知見および
その特性を用いた超塑性成型法に関するものから構成さ
れている。
However, ρ: Densification rate of powder ε: Strain rate during compression molding 2: Material constant ρ: Relative density P^: Added stress E It consists of information on superplastic forming methods using knowledge and its properties.

この場合、原料粉末(5扮)そのものが超塑性機能を有
している場合、その超塑性機能を利用して成型する。超
塑性機能を有していない6粉の金属粉または合金粉末に
超塑性を示す合金粉を混合し、混合添加した超塑性粉末
の超塑性機能によって成型する。鉄粉または合金鋼粉末
に鉄基以外の超塑性粉末を結合剤として用い、その超塑
性機能を利用して固相接合する。
In this case, if the raw material powder (5 particles) itself has a superplastic function, the superplastic function is used to mold. An alloy powder exhibiting superplasticity is mixed with six metal powders or alloy powders that do not have a superplastic function, and molded using the superplastic function of the mixed and added superplastic powder. A non-iron-based superplastic powder is used as a binder for iron powder or alloy steel powder, and solid phase bonding is performed by utilizing its superplastic function.

以上のように超塑性機能を有する粉末を用いて成型加工
することによって次のような利点が得られる。
As described above, the following advantages can be obtained by molding using a powder having a superplastic function.

(イ)成型に要する圧力が減少し、金型にかかるコスト
が低減する。
(b) The pressure required for molding is reduced, reducing the cost of molds.

C口)塑性流動がニュートン粘性流(Newt、oni
a口viscous flow)に近くなるため圧力伝
達機能が高くなりより繊細な精密成型が可能になる。
C) Plastic flow becomes Newtonian viscous flow (Newt, oni)
Since it is close to a viscous flow, the pressure transmission function is improved and more delicate precision molding is possible.

粉末の超塑性挙動について以下に詳述する。The superplastic behavior of powder will be explained in detail below.

一般に超塑性材料の変形応力(0)は、歪速度(旦し、
 m > 0.3 で表わされる。
In general, the deformation stress (0) of a superplastic material is determined by the strain rate (temperature,
It is expressed as m > 0.3.

なお、 RBの材料ではm≦0.25である。Note that m≦0.25 for the RB material.

第1図〜第5図に各種材料の緻密化率ρすなわち歪速度
εと有効圧縮応力0本との関係を示す。
FIGS. 1 to 5 show the relationship between the densification rate ρ, that is, the strain rate ε, of various materials and the effective compressive stress of zero.

第1図は水アトマイズド1.2%C鋼粉、第2図は水ア
トマイズド2.0%、C鋼(この鋼はバルク材でも超塑
性)、第3図は2.0%C−0,5%Mロー■、5%C
r−0.02%Mo鋼、第4図は1.5%−Ni−1,
0%P合金鋼扮のグラフである。なお第5図は還元純鉄
粉のグラフである。
Figure 1 shows water atomized 1.2% C steel powder, Figure 2 shows water atomized 2.0% C steel (this steel is superplastic even in bulk), Figure 3 shows 2.0% C-0, 5% M low ■, 5% C
r-0.02%Mo steel, Figure 4 shows 1.5%-Ni-1,
It is a graph of 0% P alloy steel. Note that FIG. 5 is a graph of reduced pure iron powder.

第1図〜第4図はすべてm = 0.4〜0.33(1
/ m = 2.5〜3.0 )の範囲にあり、第1図
〜第4図の鋼粉は超塑性によって圧縮成型されているこ
とを示している。第5図の還元純鉄粉の応力指数mは0
.25 (1/ m = 4.0 )で超塑性を有しな
い。なお図には示さなかったが、バルク材で超塑性を示
す組成の鋼粉例えば H3LA鋼組成の鋼粉 高速度組成鋼の銅粉 Fe−(10〜20)%Mn鋼粉 Fe−4%Ni−3%M o −1,6%Ti鋼粉Fe
−50%Cu鋼扮 およ鋼粉合金粉、N1合金粉、Sn合金扮等はすべてそ
の熱間圧縮成型過程で超塑性挙動を示した。以上のこと
がらバルク材で超塑性を発現する材料は粉末の状態でも
同様に超塑性を示すことが分る。
Figures 1 to 4 all show m = 0.4 to 0.33 (1
/ m = 2.5 to 3.0), indicating that the steel powders in Figs. 1 to 4 are compression-molded by superplasticity. The stress index m of reduced pure iron powder in Figure 5 is 0.
.. 25 (1/m = 4.0) and has no superplasticity. Although not shown in the figure, steel powder with a composition that exhibits superplasticity in the bulk material, for example, steel powder with H3LA steel composition, copper powder of high-speed composition steel Fe-(10-20)%Mn steel powder Fe-4%Ni -3%Mo -1,6%Ti steel powder Fe
-50% Cu steel, steel powder alloy powder, N1 alloy powder, Sn alloy powder, etc. all exhibited superplastic behavior during the hot compression molding process. From the above, it can be seen that materials that exhibit superplasticity in bulk also exhibit superplasticity in powder form.

また第1図〜第4図の結果から、粉末の緻密化・・・・
・・ (2) 但し、ρ、扮粉末緻富化率 ε、圧圧縮型型中歪速度 に2 物質常数 ρ:相対富度 PA−付加応力 E、ヤング率 超塑性粉末の場合 n 1.0〜3.0 D=Dgb :拉界自己拡散係rr’i (粒界拡散の
活性化エネルギーを有する) 超塑性を示さない粉末の場合 n:3.0〜5.0 D=DL :格子自己拡散係数((δ子拡散の活性化エ
ネルギーを有する) で記述される。
Also, from the results shown in Figures 1 to 4, the densification of the powder...
... (2) However, ρ, powder enrichment rate ε, strain rate in the compression mold are 2. Material constant ρ: relative enrichment PA - added stress E, Young's modulus n in case of superplastic powder is 1.0 ~ 3.0 D=Dgb: Lattice self-diffusion coefficient rr'i (has activation energy for grain boundary diffusion) For powders that do not exhibit superplasticity, n: 3.0 to 5.0 D=DL: Lattice self-diffusion It is described by the coefficient ((has the activation energy of δ ion diffusion).

すなわち、−F記(2)式において目的とする粉末の圧
縮過程における変形のための活性化エネルギーが粒界拡
散のそれに近く、かつ応力指Rnが1.0〜3.0の範
囲にある粉末を超塑性粉末とする。
That is, in Equation (2) of -F, the activation energy for deformation during the compression process of the target powder is close to that of grain boundary diffusion, and the stress index Rn is in the range of 1.0 to 3.0. is a superplastic powder.

次に、超塑性金属粉および合金粉を用いた成型法につい
て詳述する。
Next, a molding method using superplastic metal powder and alloy powder will be described in detail.

まず、超塑性機能を有する原料粉末を用いる場合につい
て説明する。この場合は、そのまま圧縮成型すればよい
訳であるが、この発展的応用として硬い微粉末(har
d  fine powder )による分散強化法が
ある6すなわち、超塑性粉末である母扮に、WC,T 
i C,Cr炭化物、N化合物、Nb化合物等の微細粉
末やまたはファインセラミックス微粉末を混合し、超塑
性による濡れ性を利用して成型すると、これらの硬い微
粉末をマトリックス中に分散させることができ、硬い微
粉末による分散強化を図ることができる。
First, a case will be described in which a raw material powder having superplastic function is used. In this case, compression molding can be done as is, but as an advanced application, hard fine powder (har
There is a dispersion strengthening method using d fine powder 6 In other words, WC, T
i By mixing fine powders such as C, Cr carbides, N compounds, Nb compounds, or fine ceramic powders and molding them using the wettability of superplasticity, it is possible to disperse these hard fine powders in the matrix. It is possible to strengthen the dispersion by using hard fine powder.

次に、超塑性機能を有した合金粉をけ合金粉に混合して
超塑性圧縮成型する方法について説明する。母合金粉を
高強度、高靭性を示す組成に成分設計し1例えば水アト
マイズ法で作成する。このけ合金粉に例えば超塑性機能
を有したFeCu合金粉を混合し、Fe−C14合金の
超塑性発現領域で圧縮成をする。超塑性変形条件の温度
は低いため、強度、靭i生を目標にM分設計し組織制御
したけ合金粉の状態はそのまま保存される。さらには 
比較的低温で拡散焼鈍してもよく、この場合は一層の緻
密性が実現される。
Next, a method of superplastic compression molding by mixing an alloy powder having a superplastic function with an alloy powder will be described. A master alloy powder is designed to have a composition that exhibits high strength and high toughness, and is prepared by, for example, a water atomization method. For example, FeCu alloy powder having a superplastic function is mixed with the Konoke alloy powder, and compression molding is performed in the superplasticity expression region of the Fe-C14 alloy. Since the temperature under superplastic deformation conditions is low, the state of the bamboo alloy powder, which is designed for M minutes and whose structure is controlled with the aim of strength and toughness, is preserved as it is. Furthermore
Diffusion annealing may also be performed at relatively low temperatures, in which case greater densification is achieved.

次に、鉄粉または高強度、高靭性を示す塑性に成分設計
した合金鋼粉をけ扮とし、鉄基合金以外の超塑性粉末を
結合剤として用いて圧縮成型する場合について説明する
。この場合も超塑性機能を有した合金鋼粉をは合金粉に
混合して超塑性成型する方法と同様に超塑性変形条件の
温度は低いため、組識制i卸したF寸鋼粉の状態はその
まま保存される。さらには低l晶での拡散焼鈍によって
、−層の緻密化を図ることができる。
Next, a case will be described in which compression molding is performed using iron powder or alloy steel powder whose composition is designed to have high strength and high toughness and plasticity as a binder, and a superplastic powder other than an iron-based alloy as a binder. In this case as well, the temperature of the superplastic deformation condition is low, similar to the method of mixing alloyed steel powder with superplasticity with alloy powder and forming it into superplasticity. will be saved as is. Furthermore, by diffusion annealing with low l crystal, the - layer can be made denser.

[実施例1 実施例1 水アトマイズド1.6%C鋼粉と商用還元純鉄粉を用い
てそれぞれ室温で相対密度が60%になるように調整し
た予圧縮材を製造し、これらをそれソh 7H度650
℃テ400 k g f/crn’)荷重テ圧縮したと
きの相対密度の変化を第6図に示した。この場合、還元
純鉄粉が相対密度約80%程度しか圧縮されないのに対
して、水アトマイズド1.6%C鋼扮鋼粉100%の相
対密度を達成することができた。
[Example 1 Example 1 Pre-compression materials were manufactured using water atomized 1.6% C steel powder and commercial reduced pure iron powder, each having a relative density of 60% at room temperature, and these were h 7H degree 650
FIG. 6 shows the change in relative density when compressed under a load of 400 kg f/crn'. In this case, while the reduced pure iron powder is compressed to a relative density of only about 80%, it was possible to achieve a relative density of 100% of the water atomized 1.6% C steel powder.

なおこの場合、1.6%C鋼扮鋼粉形のための活性化エ
ネルギーは約170kJ/mo+で鉄の粒界拡散の値に
等しく、前述の(2)式で示す応力指数n = 2.5
であるにれに対し還元純鉄粉の変形のための活性化エネ
ルギーは260kJ/molで鉄の格子拡散の値に等し
く、n = 4.0であった。
In this case, the activation energy for the 1.6% C steel powder type is about 170 kJ/mo+, which is equal to the value of grain boundary diffusion of iron, and the stress index n = 2. 5
The activation energy for deformation of reduced pure iron powder was 260 kJ/mol, which was equal to the value of iron lattice diffusion, and n = 4.0.

実施例2 第7図は水アトマイズド鋼粉A(C=1.5重量%、5
i=0.3重量%、Mn=0.5fftm%、Cr=1
.5fftffi%、M o = 0.02市川%、m
 = 2.5および水アトマイズド鋼粉B(C二O11
mu%、5i=0.3ffiu%、Mn=0.1市川%
、 Cr=0゜5重層%、m=4.0)について温度7
00°Cで、荷重0から1.5トンまで歪速度IQ/s
ecで圧縮したときの圧縮荷重に対する相対密度の変化
を小した。
Example 2 Figure 7 shows water atomized steel powder A (C = 1.5% by weight, 5% by weight).
i=0.3% by weight, Mn=0.5fftm%, Cr=1
.. 5fffffi%, M o = 0.02 Ichikawa%, m
= 2.5 and water atomized steel powder B (C2O11
mu%, 5i=0.3ffiu%, Mn=0.1 Ichikawa%
, Cr=0°5 layer%, m=4.0) at temperature 7
At 00°C, strain rate IQ/s from load 0 to 1.5 tons
The change in relative density with respect to compression load when compressed by EC was reduced.

超塑性を示す鋼粉Aは鋼粉Bと比べて容易に高密度に達
することが示されている。なお、鋼粉Aの変形のための
活性化エネルギーQは+80kJ/molで鉄の粒界拡
散の値に近く、n = 2.5であった。これに対し、
鋼粉BはQ=275kJ/mo1.n=4.0であった
It has been shown that steel powder A exhibiting superplasticity easily reaches a high density compared to steel powder B. Note that the activation energy Q for deformation of steel powder A was +80 kJ/mol, which was close to the value of grain boundary diffusion of iron, and n = 2.5. In contrast,
Steel powder B has Q=275kJ/mo1. n=4.0.

[発明の効果1 従来の焼結鍜造の温度は700〜900℃でそのときの
パンチ圧力は100〜150 k g/rnrr?(1
0−15j/crrr’)である。600〜700°C
の場合は20t/cゴとなる。一方、超塑性圧縮の場合
は700℃で、2t/cは以下で成型することができ、
成型荷重は115以下となる。
[Effect of the invention 1 The temperature of conventional sintering is 700 to 900°C, and the punch pressure at that time is 100 to 150 kg/rnrr? (1
0-15j/crrr'). 600~700°C
In this case, it becomes 20t/c. On the other hand, in the case of superplastic compression, molding can be performed at 700℃, 2t/c or less,
The molding load is 115 or less.

また1品度も100℃以上低くなる。従って、ダイスに
かかるランニングコスト、製造コストを低減し、かつ塑
性流動がニュートン流に近(なるため圧力伝達機能が高
(なり、従来の方法では不可能であった微細な精密成型
が可能となった。
In addition, the quality of one product also decreases by more than 100°C. Therefore, the running cost and manufacturing cost of the die are reduced, and the plastic flow becomes close to Newtonian flow, resulting in a high pressure transmission function, making it possible to perform fine precision molding that was impossible with conventional methods. Ta.

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

第1図〜第5図は各種粉末の圧縮成型時の歪速度と圧縮
荷重の関係を示すグラフ、第6図は相対密度の変化を示
すグラフ、第7図は荷重対相対密度の関係を示したグラ
フである。 ρ・相対密度(バルクの密度に対する圧粉体の密度の比
) DL=格子自己拡散係数 Dgb :粒界自己拡散係数 pA・付加荷重 E:ヤング率 ρ=相対密度変化率
Figures 1 to 5 are graphs showing the relationship between strain rate and compression load during compression molding of various powders, Figure 6 is a graph showing changes in relative density, and Figure 7 is a graph showing the relationship between load and relative density. This is a graph. ρ・Relative density (ratio of green compact density to bulk density) DL=Lattice self-diffusion coefficient Dgb: Grain boundary self-diffusion coefficient pA・Additional load E: Young’s modulus ρ=Relative density change rate

Claims (1)

【特許請求の範囲】 1 超塑性機能を有する粉末を用いて成型体を超塑性圧
縮成型によって製造する圧縮成型体の製造方法。 2 水アトマイズ法等により製造した粉末に後処理を施
して超塑性機能を付与し、該粉末を用いて成型体を超塑
性圧縮成型によって製造する成型体の製造方法。 3 超塑性機能を有する母粉に金属炭化物、金属窒化物
等の微細粉末またはァインセラミックス微粉末を混合添
加し、母粉の超塑性による濡れ性および超塑性流動を応
用して、成型体を圧縮成型する成型体の製造方法。 4 高強度、高靭性に成分設計した合金粉末を製造し、
該合金粉末に超塑性機能を有する粉末を添加混合し、該
添加した粉末の超塑性発現領域で該混合粉末を圧縮成型
加工する成型体の製造方法。 5 鉄粉または高強度、高靭性を示す塑性に成分設計し
た合金鋼粉を母粉とし、鉄基合金以外の超塑性粉末を結
合剤として用いて圧縮成型する請求項4記載の方法。 6 圧縮成型加工後に拡散焼鈍工程を付加した請求項4
または5記載の方法。 7 粉末の緻密化率■が式 ▲数式、化学式、表等があります▼ において、Dがその粉末の粒界自己拡散係数に近い値を
有し、かつn=0.35〜1.0の値を示す粉末を用い
て成型体を圧縮成型する成型体の製造方法。 ただし、 ■:粉末の緻密化率 K_2:物質常数 ρ:相対密度 P_A:付加応力 E:ヤング率
[Scope of Claims] 1. A method for manufacturing a compression molded body, in which the molded body is manufactured by superplastic compression molding using powder having a superplastic function. 2. A method for producing a molded body, in which a powder produced by a water atomization method or the like is post-treated to impart a superplastic function, and a molded body is produced using the powder by superplastic compression molding. 3 Add fine powders such as metal carbides and metal nitrides or fine ceramic powders to a mother powder with superplastic function, and apply the wettability and superplastic flow of the mother powder to form a molded body. A method for manufacturing a molded body by compression molding. 4. Manufacture alloy powder whose composition is designed to have high strength and high toughness,
A method for manufacturing a molded body, which comprises adding and mixing a powder having a superplastic function to the alloy powder, and compression molding the mixed powder in a region where the added powder exhibits superplasticity. 5. The method according to claim 4, wherein the mother powder is iron powder or alloyed steel powder whose composition has been designed to have plasticity that exhibits high strength and high toughness, and compression molding is performed using superplastic powder other than iron-based alloy as a binder. 6 Claim 4: A diffusion annealing process is added after compression molding.
or the method described in 5. 7 The densification rate of the powder ■ is expressed by the formula ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ where D has a value close to the grain boundary self-diffusion coefficient of the powder, and n = 0.35 to 1.0. A method for producing a molded body, comprising compression molding the molded body using a powder showing the following. However, ■: Powder densification rate K_2: Material constant ρ: Relative density P_A: Added stress E: Young's modulus
JP26159788A 1988-10-19 1988-10-19 Manufacture of green compact by using powder having super plastic function Pending JPH02111802A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26159788A JPH02111802A (en) 1988-10-19 1988-10-19 Manufacture of green compact by using powder having super plastic function

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26159788A JPH02111802A (en) 1988-10-19 1988-10-19 Manufacture of green compact by using powder having super plastic function

Publications (1)

Publication Number Publication Date
JPH02111802A true JPH02111802A (en) 1990-04-24

Family

ID=17364121

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26159788A Pending JPH02111802A (en) 1988-10-19 1988-10-19 Manufacture of green compact by using powder having super plastic function

Country Status (1)

Country Link
JP (1) JPH02111802A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0379701A (en) * 1988-11-02 1991-04-04 Quebec Metal Powders Ltd Iron powder mixture containing boron nitride suited to machining

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0379701A (en) * 1988-11-02 1991-04-04 Quebec Metal Powders Ltd Iron powder mixture containing boron nitride suited to machining

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