JP2743090B2 - How to control the carbon content of metal injection products - Google Patents

How to control the carbon content of metal injection products

Info

Publication number
JP2743090B2
JP2743090B2 JP1199676A JP19967689A JP2743090B2 JP 2743090 B2 JP2743090 B2 JP 2743090B2 JP 1199676 A JP1199676 A JP 1199676A JP 19967689 A JP19967689 A JP 19967689A JP 2743090 B2 JP2743090 B2 JP 2743090B2
Authority
JP
Japan
Prior art keywords
carbon
binder
amount
sintering
carbon content
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
JP1199676A
Other languages
Japanese (ja)
Other versions
JPH0364402A (en
Inventor
正人 三宅
和夫 岡村
義清 田中
Original Assignee
株式会社 小松製作所
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 株式会社 小松製作所 filed Critical 株式会社 小松製作所
Priority to JP1199676A priority Critical patent/JP2743090B2/en
Publication of JPH0364402A publication Critical patent/JPH0364402A/en
Application granted granted Critical
Publication of JP2743090B2 publication Critical patent/JP2743090B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Powder Metallurgy (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は金属射出品の炭素量コントロール方法に関す
る。
Description: TECHNICAL FIELD The present invention relates to a method for controlling the carbon content of a metal injection product.

(従来の技術) 一般の鉄系焼結部品を製造するに当たって、鋳鉄粉に
Fe2O3を添加して焼結性を向上させ機械的性質を向上さ
せるようにした技術が、特公昭61−3863号公報に開示さ
れているが、これは鋳鉄切削屑の利用を目的とした発明
である。
(Prior art) In producing general iron-based sintered parts, cast iron powder
A technique in which Fe 2 O 3 is added to improve sinterability and improve mechanical properties is disclosed in Japanese Patent Publication No. 61-3863, which aims to use cast iron cuttings. It is the invention which was completed.

これに対して金属粉末を焼結する場合、これら粉末に
バインダを加えて所定の形状に成形したのち焼結するも
のがあり、その成形をバインダを多量に加えて射出成形
で行う方法が試みられ、既に一部が実用化されている。
On the other hand, when sintering metal powders, there is a method in which a binder is added to these powders and then molded into a predetermined shape, followed by sintering. A method of adding a large amount of a binder and performing injection molding has been attempted. Some have already been put to practical use.

後者の場合、金属粉末と樹脂、ワックスを主成分とす
る有機物を混合し、前記有機物の流動性を利用すること
によって所望の形状を射出成形する。
In the latter case, a desired shape is injection-molded by mixing a metal powder, an organic substance mainly composed of resin and wax, and utilizing the fluidity of the organic substance.

そして成形体はその形状を保持したまま、比較的低温
で加熱されることによって有機物の大部分は分解、除去
される。
The molded body is heated at a relatively low temperature while maintaining its shape, so that most of the organic matter is decomposed and removed.

脱バインダ後の成形体は、その後の本焼結の工程に移
行するまでの間、ハンドリング、移送等の作業によって
破壊されることのないよう、通常当初の投入バインダ量
の4重量%から15重量%残すようにしている。
The molded body after the binder removal is usually from 4% by weight to 15% by weight of the initially input binder amount so as not to be destroyed by handling, transfer and the like until the process proceeds to the subsequent main sintering step. %.

その後の本焼結において、残りのバインダの大部分は
分解除去されるが、その一部が炭素となって金属焼結体
に残留することになる。
In the subsequent main sintering, most of the remaining binder is decomposed and removed, but part of it becomes carbon and remains in the metal sintered body.

(発明が解決しようとする課題) しかしながら、脱バインダ工程は通常N2,Ar等の不活
性ガス雰囲気あるいは大気中で実施されるものであるか
ら、不活性ガス雰囲気で脱脂を実施した場合、使用する
バインダの種類ならびに金属粉との配合割合によって異
なるが、一例として、バインダの使用割合を45体積%と
した場合の平均4μmの鉄粉を用いた焼結体に残留する
炭素量は表1に示すようになる。
(Problems to be Solved by the Invention) However, since the debinding step is usually performed in an inert gas atmosphere such as N 2 , Ar or the like or in the air, if degreasing is performed in an inert gas atmosphere, Depending on the type of binder to be used and the mixing ratio with the metal powder, as an example, the amount of carbon remaining in the sintered body using an average 4 μm iron powder when the binder usage ratio is 45 vol% is shown in Table 1. As shown.

焼結体に所望する炭素量がこれらバインダから入る炭
素量では足りない場合は、さらに黒鉛粉を添加すること
で炭素分を増加させれば良く、製法上問題とならない。
If the desired amount of carbon in the sintered body is not sufficient with the amount of carbon entering from these binders, the amount of carbon may be increased by further adding graphite powder, and there is no problem in the production method.

しかしながら、焼結体に所望する炭素量より多い炭素
量がバインダから入る場合、なんらかの方法で炭素量を
精度良く減少させなければならず、しかも現実にはこう
したケースの方が圧倒的に多く問題であった。
However, when the amount of carbon larger than the desired amount of carbon enters the sintered body from the binder, the amount of carbon must be accurately reduced by some method, and in reality, such a case is overwhelmingly more problematic. there were.

本発明は、これに鑑みバインダが供給源となって焼結
体に必要以上に残留する炭素を酸化させることにより、
所望する炭素量に精度良く減じ、かつ炭素の偏析がなく
均一な組織を得ることのできる金属射出成形品の炭素量
コントロール方法を提供して、従来技術の持つ欠点の解
消を図ることを目的としてなされたものである。
In view of this, the present invention oxidizes carbon remaining unnecessarily in the sintered body with the binder serving as a supply source,
The object of the present invention is to provide a method for controlling the carbon content of a metal injection-molded product capable of accurately reducing to a desired carbon content and obtaining a uniform structure without carbon segregation, and to solve the disadvantages of the prior art. It was done.

(課題を解決するための手段) 上記目的を達成するため本願請求項1の発明は、焼結
用鉄粉を55〜65体積%と、有機物バインダを35〜45体積
%とからなる射出成形品を、脱バインダの工程を経たの
ち焼結するとき、前記原料粉である焼結用鉄粉にFe2O3,
Fe3O4,Cu2O,NiO,CoO,Cr2O3,MnO,V2O3等の金属酸化物を
一種以上添加して、還元性もしくは非酸化性雰囲気で焼
結することにより、前記バインダが供給源となって必要
以上に残留する炭素を所望の炭素量に制御することを特
徴とする。本願請求項2の発明は、請求項1の発明にお
いて、前記金属酸化物の平均粒径は1〜2.5μmの大き
さであることを特徴とする。
(Means for Solving the Problems) In order to achieve the above object, the invention of claim 1 of the present application is directed to an injection molded product comprising 55 to 65% by volume of iron powder for sintering and 35 to 45% by volume of an organic binder. When sintering after passing through the binder removal process, Fe 2 O 3 ,
By adding one or more metal oxides such as Fe 3 O 4 , Cu 2 O, NiO, CoO, Cr 2 O 3 , MnO, V 2 O 3 and sintering in a reducing or non-oxidizing atmosphere, The binder serves as a supply source to control carbon remaining more than necessary to a desired carbon amount. According to a second aspect of the present invention, in the first aspect, the metal oxide has an average particle size of 1 to 2.5 μm.

(作用) 請求項1の発明によれば、焼結用鉄粉にバインダが供
給源となって必要以上に焼結体に残留する炭素を所望の
炭素量に精度良く減じ、かつ均一にコントロールできる
ため、炭素の偏析がなく、均一な組織が得られる。
(Function) According to the first aspect of the present invention, the amount of carbon remaining in the sintered body more than necessary with the binder as a supply source for the iron powder for sintering can be accurately reduced to a desired amount of carbon, and can be uniformly controlled. Therefore, a uniform structure without carbon segregation can be obtained.

請求項2の発明によれば、金属酸化物の平均粒径を1
〜2.5μmの大きさにして金属酸化物の粒径の微細化を
防止したので、射出成形・金型内冷却時において、金属
酸化物の熱伝導性が悪くても焼結用鉄粉同士の熱伝導を
阻害することなく、内部応力の小さい成形体が作られる
ため、脱脂時にクラックが発生することがない。
According to the invention of claim 2, the average particle size of the metal oxide is 1
Since the size of the metal oxide is reduced to 2.5 μm to prevent the metal oxide particle size from becoming fine, during injection molding and cooling in the mold, even if the thermal conductivity of the metal oxide is poor, Since a compact having a small internal stress is produced without hindering heat conduction, cracks do not occur during degreasing.

(実施例) 以下、本発明を比較例及び各実施例を参照して説明す
る。
(Examples) Hereinafter, the present invention will be described with reference to Comparative Examples and Examples.

比較例 平均粒径4μm、炭素量0.01%、酸素量0.2%の球状
鉄粉4290gに、 (1).マイクロクリスタリンワックスを主成分とする
バインダ、 (2).マイクロクリスタリンワックスと低分子量アク
リル(分子量55000)を等分に配合したものを主成分と
するバインダ、 (3).ポリアミドを主成分とするバインダ、 を391.5g(8.36重量%)添加し、加圧ニーダにより140
℃で2時間混練して、この混練物を粉砕し射出成形機に
投入した。
Comparative Example To 4290 g of spherical iron powder having an average particle size of 4 μm, a carbon content of 0.01% and an oxygen content of 0.2%, (1). A binder mainly composed of microcrystalline wax; (2). (3) a binder mainly composed of a mixture of microcrystalline wax and low molecular weight acrylic (molecular weight: 55,000) in equal proportions; 391.5g (8.36% by weight) of a binder containing polyamide as a main component was added, and 140
The mixture was kneaded at 2 ° C. for 2 hours, and the kneaded product was pulverized and put into an injection molding machine.

そしてφ5×501の棒状試験片を1ton/cm2の成形圧で
射出成形した。
Then, a rod-shaped test piece of φ5 × 501 was injection-molded at a molding pressure of 1 ton / cm 2 .

つぎに成形品をN2雰囲気中で500℃まで10℃/hrの速度
で昇温し、2hr保持したのち炉冷した。その後真空炉で1
250℃で1hr焼結し、相対密度95〜97%の焼結品を得た。
Next, the molded product was heated to 500 ° C. at a rate of 10 ° C./hr in an N 2 atmosphere, and was held for 2 hours and then cooled in a furnace. Then in a vacuum furnace 1
Sintering was performed at 250 ° C for 1 hour to obtain a sintered product having a relative density of 95 to 97%.

このときのそれぞれ20本づつの焼結品の炭素量の分析
結果を表1に示す。
Table 1 shows the analysis results of the carbon content of each of the 20 sintered products at this time.

実施例1. 比較例で使用した4μm鉄粉と平均粒径2μmのFe2O
3粉を表2に示す配合によりV形混粉機にて30分混粉し
た。
Example 1. 4 μm iron powder used in Comparative Example and Fe 2 O having an average particle size of 2 μm
The three powders were mixed in a V-type mixer for 30 minutes according to the composition shown in Table 2.

そしてそれぞれの混合物4290gにポリアミドを主成分
とするバインダを391.5g(8.36重量%)添加し、加圧ニ
ーダにより140℃で2時間混練した。この混練物を粉砕
し射出成形機に投入した。
Then, 391.5 g (8.36% by weight) of a binder containing polyamide as a main component was added to 4290 g of each mixture, and kneaded at 140 ° C. for 2 hours by a pressure kneader. This kneaded product was pulverized and put into an injection molding machine.

φ5×501の棒状試験片を1ton/cm2の成形圧で射出成
形した。
A rod-shaped test piece of φ5 × 501 was injection molded at a molding pressure of 1 ton / cm 2 .

つぎに成形品各5本をN2雰囲気中で500℃まで10℃/hr
の速度で昇温し、2hr保持したのち炉冷した。その後脱
脂した試料各5本を真空炉で1250℃で1hr焼結し、相対
密度95〜97%の焼結品を得た。
Next, each of the 5 molded products is 10 ° C / hr up to 500 ° C in N 2 atmosphere.
The temperature was raised at the rate described above, the temperature was maintained for 2 hours, and then the furnace was cooled. Thereafter, each of the five degreased samples was sintered in a vacuum furnace at 1250 ° C for 1 hour to obtain a sintered product having a relative density of 95 to 97%.

Fe2O3の添加量と残留炭素の関係を図に示す。これに
よれば添加量に応じて、残留炭素量をコントロールでき
ることが分かる。
The relationship between the amount of Fe 2 O 3 added and the residual carbon is shown in the figure. According to this, it can be seen that the amount of residual carbon can be controlled according to the amount of addition.

そしてバラツキはそれぞれ最大で0.1%Cの範囲内に
精度良く納まった。
The variation was within the range of 0.1% C at maximum with high accuracy.

実施例2. 比較例で使用した4μm鉄粉4035gに、2%Ni−1.5%
Cu−0.2%Cを成分のねらい値として、平均粒径1μm
のNiO粉109g、平均粒径2.5μmのCu2O粉を73g、平均粒
径2μmのFe2O3粉を73g添加し、合計4290gの粉末をV
形混粉機で30分間混粉した。この混合粉4290gにポリア
ミドを主成分とするバインダを391.5g(8.36重量%)添
加し、加圧ニーダにより140℃で2時間混練して、この
混練粉を粉砕し、φ5×501の棒状試験片を1ton/cm2
成形圧で射出成形した。
Example 2. To 4035 g of the 4 μm iron powder used in the comparative example, 2% Ni-1.5%
The average particle diameter is 1 μm, with Cu-0.2% C as the target value of the component.
109 g of NiO powder, 73 g of Cu 2 O powder having an average particle size of 2.5 μm, and 73 g of Fe 2 O 3 powder having an average particle size of 2 μm were added.
The mixture was mixed for 30 minutes with a shape mixer. To 4290 g of the mixed powder, 391.5 g (8.36% by weight) of a binder containing polyamide as a main component was added and kneaded at 140 ° C. for 2 hours by a pressure kneader, and the kneaded powder was pulverized into a rod-shaped test piece of φ5 × 501. Was injection molded at a molding pressure of 1 ton / cm 2 .

つぎに成形品をN2雰囲気中で500℃まで10℃/hrの速度
で昇温し2hr保持したのち炉冷した。その後真空炉で125
0℃で1hr焼結し、Ni,Cu,Cの各元素について分析を実施
したところ、2.04%Ni−1.52%Cu−0.22%Cとほぼねら
い値通りの鉄系焼結品が得られた。このように金属酸化
物を適宜組み合わせて目標成分を持つ焼結合金が可能と
なる。
Next, the molded article was heated to 500 ° C. at a rate of 10 ° C./hr in an N 2 atmosphere, kept for 2 hr, and then cooled in a furnace. Then in a vacuum furnace 125
After sintering at 0 ° C. for 1 hour, the analysis of each element of Ni, Cu, and C was carried out. As a result, an iron-based sintered product almost at the target value of 2.04% Ni-1.52% Cu-0.22% C was obtained. Thus, a sintered alloy having a target component can be obtained by appropriately combining metal oxides.

本実施例では金属酸化物の粒径が1〜2.5μmのと
き、焼結用鉄粉の平均粒径は4μmであり、(金属酸化
物/焼結用鉄粉)の粒径の比は、0.25〜0.625となる。
In this example, when the particle size of the metal oxide is 1 to 2.5 μm, the average particle size of the iron powder for sintering is 4 μm, and the ratio of the particle size of (metal oxide / iron powder for sintering) is as follows: It becomes 0.25 to 0.625.

勿論金属酸化物の構成により炭素量が不足する場合は
黒鉛物を必要量添加しておけば良いことになる。
Of course, if the amount of carbon is insufficient due to the configuration of the metal oxide, the required amount of graphite may be added.

(発明の効果) 本発明は以上説明したように請求項1によれば、
(1)焼結体に残留する炭素を所望の炭素量に精度良く
減じることにより、所望の炭素量を含む焼結体が得られ
る。従って、残留炭素分の多いバインダを使用する場合
であっても低い炭素部品に適用することができる。
(Effect of the Invention) As described above, according to the first aspect of the present invention,
(1) By accurately reducing the amount of carbon remaining in the sintered body to a desired amount of carbon, a sintered body containing the desired amount of carbon can be obtained. Therefore, even when a binder having a large residual carbon content is used, the present invention can be applied to a low carbon component.

(2)焼結体に残留する炭素を均一にコントロールでき
るため、炭素の偏析がなく、均一な組織が得られるた
め、材料強度が向上する。
(2) Since the carbon remaining in the sintered body can be uniformly controlled, there is no segregation of carbon and a uniform structure can be obtained, so that the material strength is improved.

請求項2によれば、(3)請求項1において金属酸化
物の粒径を1〜2.5μmとすることにより、金属酸化物
の比表面積の増大を抑えて、成形時に金属酸化物をコー
ティングするバインダの量を低減して製造コストの低減
を図ることができる。
According to the second aspect, (3) the metal oxide is coated at the time of molding by suppressing the increase in the specific surface area of the metal oxide by setting the particle diameter of the metal oxide to 1 to 2.5 μm in the first aspect. By reducing the amount of the binder, the manufacturing cost can be reduced.

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

図面は本発明にかかる金属射出品の炭素量コントロール
方法によるFe2O3の添加量と残留炭素量との関係を示す
グラフである。
The drawing is a graph showing the relationship between the amount of added Fe 2 O 3 and the amount of residual carbon by the method for controlling the amount of carbon in a metal injection product according to the present invention.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 田中 義清 大阪府枚方市上野3―1―1 株式会社 小松製作所生産技術研究室内 (56)参考文献 特開 平2−57607(JP,A) ────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yoshikiyo Tanaka 3-1-1 Ueno, Hirakata-shi, Osaka Komatsu Manufacturing Co., Ltd. (56) References JP-A-2-57607 (JP, A)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】焼結用鉄粉を55〜65体積%と、有機物バイ
ンダを35〜45体積%とからなる射出成形品を、脱バイン
ダの工程を経たのち焼結するとき、前記原料粉である焼
結用鉄粉にFe2O3,Fe3O4,Cu2O,NiO,CoO,Cr2O3,MnO,V2O3
等の金属酸化物を一種以上添加して、還元性もしくは非
酸化性雰囲気で焼結することにより、前記バインダが供
給源となって必要以上に残留する炭素を所望の炭素量に
制御することを特徴とする金属射出品の炭素量コントロ
ール方法。
1. An injection molded product comprising 55 to 65% by volume of iron powder for sintering and 35 to 45% by volume of an organic binder is sintered after passing through a binder removing step. Fe 2 O 3 , Fe 3 O 4 , Cu 2 O, NiO, CoO, Cr 2 O 3 , MnO, V 2 O 3
By adding one or more metal oxides, etc., and sintering in a reducing or non-oxidizing atmosphere, the binder serves as a supply source to control unnecessarily remaining carbon to a desired amount of carbon. Characteristic method for controlling carbon content of metal injection products.
【請求項2】前記金属酸化物の平均粒径は1〜2.5μm
の大きさであることを特徴とする請求項1記載の金属射
出品の炭素量コントロール方法。
2. The metal oxide has an average particle size of 1 to 2.5 μm.
2. The method for controlling the carbon content of a metal injection product according to claim 1, wherein
JP1199676A 1989-07-31 1989-07-31 How to control the carbon content of metal injection products Expired - Lifetime JP2743090B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1199676A JP2743090B2 (en) 1989-07-31 1989-07-31 How to control the carbon content of metal injection products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1199676A JP2743090B2 (en) 1989-07-31 1989-07-31 How to control the carbon content of metal injection products

Publications (2)

Publication Number Publication Date
JPH0364402A JPH0364402A (en) 1991-03-19
JP2743090B2 true JP2743090B2 (en) 1998-04-22

Family

ID=16411763

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1199676A Expired - Lifetime JP2743090B2 (en) 1989-07-31 1989-07-31 How to control the carbon content of metal injection products

Country Status (1)

Country Link
JP (1) JP2743090B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH089721B2 (en) * 1990-03-22 1996-01-31 松下電工株式会社 Manufacturing method of powder sintered product
JPH06172810A (en) * 1992-10-08 1994-06-21 Kawasaki Steel Corp Production of tungsten alloy sintered compact
JPH06346168A (en) * 1993-06-03 1994-12-20 Sumitomo Metal Mining Co Ltd Ti or ti-fe injection-molded and sintered alloy and its production
JP5604981B2 (en) 2009-05-28 2014-10-15 Jfeスチール株式会社 Iron-based mixed powder for powder metallurgy
JP5663974B2 (en) * 2009-06-26 2015-02-04 Jfeスチール株式会社 Iron-based mixed powder for powder metallurgy
GB0917988D0 (en) 2009-10-14 2009-12-02 Johnson Matthey Plc Method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0257607A (en) * 1988-08-20 1990-02-27 Kawasaki Steel Corp Injection-molding powder and production of metallic sintered body

Also Published As

Publication number Publication date
JPH0364402A (en) 1991-03-19

Similar Documents

Publication Publication Date Title
JP2843900B2 (en) Method for producing oxide-particle-dispersed metal-based composite material
CN109576546A (en) A kind of preparation method of the high-strength tenacity without magnetic Ti (C, N) based ceramic metal
JP2743090B2 (en) How to control the carbon content of metal injection products
EP0523658B1 (en) Method for making injection molded soft magnetic material
JP4779997B2 (en) Method for manufacturing sintered body
JPH04329801A (en) Production of sintered parts
JP2010222661A (en) Metal powder and sintered compact
US20090291011A1 (en) Reaction sintered zirconium carbide/tungsten composite bodies and a method for producing the same
JP4877997B2 (en) Method for producing sintered hard alloy
KR970001558B1 (en) Method for composite powder
JP4161299B2 (en) Sintering method using tungsten-copper composite powder, sintered body, and heat sink
JP2793938B2 (en) Manufacturing method of sintered metal parts by metal powder injection molding method
JP3265463B2 (en) Method for producing Ti sintered body
JPS5895658A (en) Manufacture of silicon nitride sintered body
JPH0339402A (en) Manufacture of metal powder sintered body
JP4158015B2 (en) Method for producing sintered body and sintered body
JPH03173702A (en) Production of sintered body
JPH06172810A (en) Production of tungsten alloy sintered compact
JPH0142341B2 (en)
JPH11181501A (en) Production of metal powder and sintered body
JP2005068483A (en) Production method for sintered compact of mn-based high-damping alloy
JPH05263177A (en) Manufacture of nb3al intermetallic compound base alloy having a15 type crystalline structure
JPH10147832A (en) Manufacture of 'permalloy(r)' sintered compact
JPH03191002A (en) Method for removing binder and for sintering for metal injection molding product
JP3300420B2 (en) Alloy for sintered sealing material

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090206

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100206

Year of fee payment: 12

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100206

Year of fee payment: 12