JPH0238502A - Metal powder composition for injection molding and manufacture of metal sintered member - Google Patents
Metal powder composition for injection molding and manufacture of metal sintered memberInfo
- Publication number
- JPH0238502A JPH0238502A JP18869488A JP18869488A JPH0238502A JP H0238502 A JPH0238502 A JP H0238502A JP 18869488 A JP18869488 A JP 18869488A JP 18869488 A JP18869488 A JP 18869488A JP H0238502 A JPH0238502 A JP H0238502A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- injection molding
- metal powder
- parts
- binder
- 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.)
- Granted
Links
- 239000002184 metal Substances 0.000 title claims abstract description 41
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 41
- 239000000843 powder Substances 0.000 title claims abstract description 41
- 238000001746 injection moulding Methods 0.000 title claims abstract description 26
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000011230 binding agent Substances 0.000 claims abstract description 40
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 claims abstract description 14
- 239000004793 Polystyrene Substances 0.000 claims abstract description 13
- 229920002223 polystyrene Polymers 0.000 claims abstract description 13
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 12
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 abstract description 9
- 238000010438 heat treatment Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- 239000008188 pellet Substances 0.000 abstract description 4
- 238000005245 sintering Methods 0.000 abstract description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 10
- 239000000919 ceramic Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 238000002347 injection Methods 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- 238000000465 moulding Methods 0.000 description 7
- 239000001993 wax Substances 0.000 description 6
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 239000012778 molding material Substances 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 210000003127 knee Anatomy 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000010963 304 stainless steel Substances 0.000 description 1
- 229910000619 316 stainless steel Inorganic materials 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910000589 SAE 304 stainless steel Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
「産業上の利用分野」
本発明は射出成形用金属粉末組成物、及びそれを使用す
る金属焼結部材の製造法に関するもので「従来の技術」
一般に、セラミックスの分野では原料粉体に有機バイン
ダーを配合した混合物に可塑性を付与し、射出成形法に
よりグリーン成形体を得た後、これを脱バインダー焼成
することにより、プレス成形などでは成形不可能な複雑
形状のものを、寸法精度よく量産できることがよく知ら
れている。Detailed Description of the Invention "Field of Industrial Application" The present invention relates to a metal powder composition for injection molding and a method for producing a metal sintered member using the same. "Prior Art" Generally, the field of ceramics. Then, by adding plasticity to a mixture of raw material powder and an organic binder, and obtaining a green molded body using an injection molding method, the binder is removed and the green molded body is fired, thereby creating products with complex shapes that cannot be molded by press molding etc. It is well known that it can be mass-produced with good dimensional accuracy.
一方、金属焼結部材では古くから、原料粉体に若干の有
機物を混入し、プレス成形法により成形後、焼結するこ
とによる、いわゆる粉末冶金法によって製造されてきた
が、近年、高密度の複雑形状部材を量産性よく製造する
ために、上記のセラミックス製品の製造に用いられてい
る射出成形法を、金属焼結部材の製造に応…しようとい
う試みがなされている。On the other hand, metal sintered parts have long been manufactured using the so-called powder metallurgy method, in which raw material powder is mixed with a small amount of organic matter, molded using a press molding method, and then sintered. In order to mass-produce members with complex shapes, attempts have been made to adapt the injection molding method used for producing the above-mentioned ceramic products to the production of metal sintered members.
「発明が解決しようとする課題」
射出成形法による金属焼結部材の製造では、セラミック
スの原料粉末の平均粒径が3gm以下と微細であるのに
対し、
金属焼結部材のそれは、
・相対的に粗い粒度をもつこと、
・金属焼結部材に用いられる原料粉末は一般のセラミッ
クス粉末、例えばアルミナなどに比べて比重の高い場合
が多いこと、
・一般のセラミックス粉末、例えばアルミナなどの酸化
物系セラミックスに比べると、バインダー類とのぬれ性
がわるいこと
などの理由で、セラミックス製品製造の場合と同様な条
件で製造しようとしても射出成形性不良、グリーン成形
体の強度不足、脱バインダー時の変形などセラミックス
のように良好な焼結部材を製造することが困難であるば
かりか、前工程のグリーン成形体ですら満足に製造する
ことができないのが現状である。``Problem to be solved by the invention'' In the production of metal sintered parts using the injection molding method, the average particle size of the raw material powder for ceramics is as fine as 3 gm or less;・The raw material powder used for metal sintered parts often has a higher specific gravity than general ceramic powder, such as alumina. ・General ceramic powder, such as oxide-based powder such as alumina. Compared to ceramics, it has poor wettability with binders, so even if you try to manufacture it under the same conditions as when manufacturing ceramic products, you will experience poor injection moldability, insufficient strength of the green molded product, and deformation when removing the binder. Not only is it difficult to manufacture good sintered members such as ceramics, but the current situation is that even green molded bodies in the previous process cannot be manufactured satisfactorily.
本発明は、上記のような実情に鑑みなされたものであっ
て、射出成形法によって複雑な形状を有し、かつ高密度
な金属焼結部材を工業的に量産性よく製造できるような
射出成形用金属粉末組成物及び金属焼結部材の製造法を
提供することを課題とするものである。The present invention has been made in view of the above-mentioned circumstances, and is an injection molding method that enables industrial production of high-density sintered metal members with complex shapes and high mass productivity. An object of the present invention is to provide a metal powder composition for use in metal powder compositions and a method for producing a metal sintered member.
「課題を解決するための手段及び作用」本発明は、金属
粉末100重量部に対して、有機バインダー5〜15重
量部を配合してなる射出成形用金属粉末組成物において
、
有機バインダーが、ポリスチレン5〜30重量%、ポリ
ブチルメタクリレート5〜35重電%及びエチレン酢酸
ビニル共重合体5〜25重置%を必須成分として含有す
ることを特徴とする射出成形用金属粉末組成物及びそれ
を使用する金属焼結部材の製造法である。"Means and Effects for Solving the Problems" The present invention provides a metal powder composition for injection molding in which 5 to 15 parts by weight of an organic binder is blended with 100 parts by weight of metal powder, wherein the organic binder is polystyrene. A metal powder composition for injection molding, characterized in that it contains as essential components 5 to 30% by weight of polybutyl methacrylate, 5 to 35% by weight of polybutyl methacrylate, and 5 to 25% by weight of ethylene vinyl acetate copolymer, and its use. This is a method for manufacturing sintered metal parts.
(手段を構成する要件)
本発明に使用する有機バインダーとしてはポリスチレン
、ポリブチルメタクリレート及びエチレン酢酸ビニル共
重合体からなる熱可塑性樹脂を必須成分として含有する
ものである。(Requirements constituting the means) The organic binder used in the present invention contains as an essential component a thermoplastic resin consisting of polystyrene, polybutyl methacrylate, and ethylene-vinyl acetate copolymer.
ポリスチレン、ポリブチルメタクリレート及びエチレン
酢酸ビニル共重合体は、いずれも公知の市販されてい・
るものであり、それらの配合割合は、有機バインダー中
にポリスチレンが5〜30重量%、ポリブチルメタクリ
レートが5〜35重量%、エチレン酢酸ビニル共重合体
が5〜25重量%存在するよう配合されるものである。Polystyrene, polybutyl methacrylate, and ethylene vinyl acetate copolymer are all known commercially available products.
The blending ratios are such that the organic binder contains 5 to 30% by weight of polystyrene, 5 to 35% by weight of polybutyl methacrylate, and 5 to 25% by weight of ethylene vinyl acetate copolymer. It is something that
有機バインダーにおける熱可塑性樹脂各々の作用及び配
合割合について言えば、ポリスチレンは、粉体に対して
優れたバインダー効果を有し粒子同士を強く結合し、ま
たそれ自身、非常に射出成形性の良い熱可塑性樹脂であ
って、グリーン成形体に強度を付与し、特に肉薄部の破
損防止などに有効であり、さらにグリーン成形体に優れ
た保形性を付与し、成形体のハンドリングを容易にする
ものであるが、その配合量が5重量%未満の場合、前記
の効果が得られず30重量%を越えた場合、混合物の流
動性が低下し、射出成形性が損なわれる。ポリブチルメ
タクリレートは、ポリスチレン同様、粉体に対し優れた
バインダー効果を示しグリーン成形体の強度付与に大変
有効な熱可塑性樹脂である。ポリスチレン、エチレン酢
酸ビニル共重合体が300℃以上でなければ実質的に熱
分解が開始されないのに対し、ポリブチルメタクリレー
トは220〜240℃で熱分解が起こることから、これ
ら三成分の共存系においては、バインダーの熱分解温度
範囲が広がり、加熱分解で脱バインダーをする場合、バ
インダーの熱分解が急激に起こらず徐々に進行するため
、成形体のフクレ、亀裂、変形などの防止に大変有効で
あるが、その配合量が5重量%未満の場合前記の効果が
得られず、35重量%を越えた場合、混合物の流動性が
低下し、射出成形性が損なわれ、金型からの離型が悪く
なる。Regarding the action and blending ratio of each thermoplastic resin in the organic binder, polystyrene has an excellent binder effect on powders, strongly bonds particles together, and is itself a thermoplastic resin with very good injection moldability. A plastic resin that imparts strength to green molded bodies, is particularly effective in preventing damage to thin parts, and also provides excellent shape retention to green molded bodies, making the molded bodies easier to handle. However, if the amount is less than 5% by weight, the above effects cannot be obtained, and if it exceeds 30% by weight, the fluidity of the mixture decreases and the injection moldability is impaired. Polybutyl methacrylate, like polystyrene, is a thermoplastic resin that exhibits an excellent binder effect on powder and is very effective in imparting strength to green molded products. Polystyrene and ethylene-vinyl acetate copolymers do not substantially start thermal decomposition unless it is above 300°C, whereas polybutyl methacrylate undergoes thermal decomposition at 220 to 240°C, so in a system in which these three components coexist, The thermal decomposition temperature range of the binder is expanded, and when removing the binder by thermal decomposition, the thermal decomposition of the binder does not occur suddenly but proceeds gradually, making it very effective in preventing blisters, cracks, deformation, etc. of molded objects. However, if the amount is less than 5% by weight, the above effect cannot be obtained, and if it exceeds 35% by weight, the fluidity of the mixture decreases, injection moldability is impaired, and release from the mold becomes difficult. becomes worse.
さらにエチレン酢酸ビニル共重合体も粉体に対し優れた
バインダー効果を示し、グリーン成形体の強度を高め、
成形体に弾性を付与する。また。Furthermore, ethylene vinyl acetate copolymer also shows an excellent binder effect on powder, increasing the strength of green molded products,
Adds elasticity to the molded body. Also.
混合物の流動性を高め、射出成形を容易にならしめるば
かりか、加熱分解で脱バインダー処理をする場合能の成
分が熱分解して除去されている間、成形体の形状を保つ
作用を有するものであるが、その配合量が5%未満の場
合前記の効果が得られず、25%を越えた場合加熱分解
で脱バインダー処理する時、成形体のフクレ現象が顕著
となり、脱バインターを困難に至らしめる。A substance that not only increases the fluidity of the mixture and makes injection molding easier, but also maintains the shape of the molded product while the functional components are thermally decomposed and removed during binder removal treatment by thermal decomposition. However, if the amount is less than 5%, the above effect cannot be obtained, and if it exceeds 25%, the blistering phenomenon of the molded product becomes noticeable when removing the binder by thermal decomposition, making it difficult to remove the binder. bring about.
また本発明の有機へインターは、必要に応じてワックス
、可塑弁]、潤滑剤等の添加剤を適宜含有するものであ
る。In addition, the organic interlayer of the present invention contains additives such as wax, plastic valve], lubricant, etc. as necessary.
これらの成分は、混合物に可塑性を付与し流動性を向上
させ、また粉体とのぬれ性を高め、1尾合物を均一化す
る作用を有するものである。These components have the effect of imparting plasticity to the mixture, improving fluidity, increasing wettability with powder, and making the monomer mixture uniform.
ワックスとしては、例えばパラフィンワックス、マイク
ロクリスタリンワックス等、可塑剤としては、例えばジ
オクチルフタレート、シプチルフタレ−1・等、
潤滑剤としては、例えばステアリン酸、ステアリン酸金
属塩等が挙げられ、通常セラミックスの射出成形に使用
されるものなら、いかなるものも使用可能である。Waxes include paraffin wax and microcrystalline wax; plasticizers include dioctyl phthalate and cyptyl phthalate-1; lubricants include stearic acid and metal salts of stearate; and they are usually used for ceramic injection. Any material used for molding can be used.
また、これらの成分は、通常の使用範囲で用いられるの
が好ましく、ここでは特にその使用量は限定しないが、
常識を越えて使用された場合、グリーン成形体の強度が
著しく低下したり、加熱分解で脱パインター処理する場
合、著しく変形を生じたすすることは言うまでもない。In addition, these components are preferably used within the normal usage range, and the amounts used are not particularly limited here;
Needless to say, if used beyond common sense, the strength of the green molded product will drop significantly, and when depintering is performed by thermal decomposition, significant deformation will occur.
次に本発明に使用する金属粉末としては、例えばステン
レス鋼粉末、カーボニル鉄粉末等が挙げられる。Next, examples of the metal powder used in the present invention include stainless steel powder, carbonyl iron powder, and the like.
これらの粒径(平均粒径)は1〜50用mであることが
好ましい。平均粒径が1gm未満と細かくなると、相対
的に粉末の比表面積が増大し、バインダーの使用量を増
やしても多くの場合射出成形に適した流動特性を有する
混合物を得るのが困難になり、また射出成形可能でも、
その後の脱バインダー工程を円滑に行うことが難しく脱
バインダー後の成形体はもろくハンドリングが困難とな
る。一方、50pLmを越えた粗い粒度の粉末の場合、
グリーン成形体及び脱パインター後の加熱成形体の強度
が著しく低下する。The particle size (average particle size) of these particles is preferably 1 to 50 m. When the average particle size becomes smaller than 1 gm, the specific surface area of the powder increases relatively, and even if the amount of binder used is increased, it is often difficult to obtain a mixture with flow characteristics suitable for injection molding. Also, although injection molding is possible,
It is difficult to perform the subsequent binder removal step smoothly, and the molded product after binder removal becomes brittle and difficult to handle. On the other hand, in the case of coarse powder exceeding 50 pLm,
The strength of the green molded body and the heated molded body after depaintering is significantly reduced.
本発明にかかる射出成形用金属粉末組成物は前記金属粉
末100重量部に対し前記有機パインター5〜15重量
部を配合したものである。The metal powder composition for injection molding according to the present invention is one in which 5 to 15 parts by weight of the organic pinter is blended with 100 parts by weight of the metal powder.
有機パインターの使用量が、5重量部未満の場合射出成
形用材料としての混合物の流動性が不足し、所望の形状
に成形することが困難となり、一方15重量部を越えた
場合、成形品の密度が−ヒがらず、焼成時における収縮
が大きくなり、寸法精度をおとすばかりか、加熱分解に
より脱バインダーを行なう場合、多量のガスが発生し、
著しく困難となる。If the amount of organic painter used is less than 5 parts by weight, the mixture as an injection molding material will lack fluidity and it will be difficult to mold it into the desired shape, while if it exceeds 15 parts by weight, the molded product will be The density does not decrease, shrinkage increases during firing, and dimensional accuracy is reduced, and when removing the binder by thermal decomposition, a large amount of gas is generated.
becomes extremely difficult.
本発明にかかる射出成形用金属粉末組成物を用いた金属
焼結部材の製造は、以下のようにして行なうものである
。A metal sintered member using the metal powder composition for injection molding according to the present invention is produced as follows.
まず、本発明の組成物である金属粉末と有機バインダー
を加圧ニーターのような混練機で十分加熱混練し、有機
バインダー中に金属粉末を均一に分散させた後、適当な
形状、例えば粗粉砕物又はベレット状にし、射出成形用
材料とする。First, the metal powder that is the composition of the present invention and the organic binder are sufficiently heated and kneaded using a kneader such as a pressure kneader to uniformly disperse the metal powder in the organic binder, and then crushed into an appropriate shape, for example, coarsely pulverized. It is made into pellets or pellets and used as an injection molding material.
次にこの材料を通常ブラスチンク成形で使用されている
公知の装置及び方法により、射出成形し、所望の形状の
成形体とする。Next, this material is injection molded using a known device and method commonly used in blast molding to form a molded product of a desired shape.
この後、成形体より加熱分解などの方法で有機バインダ
ーを除去し、適宜最適の温度及び雰囲気で焼成すること
により所望の形状の金属焼結部材が得られる。Thereafter, the organic binder is removed from the molded body by a method such as thermal decomposition, and the molded body is fired at an appropriate temperature and atmosphere to obtain a metal sintered member having a desired shape.
金属粉末の射出成形では、使用される金属粉末に適した
有機バインダーの組合せ、配合割合、使用量を求めるこ
とが非常に大切であり、特に必須成分である熱可塑樹脂
は重要で、その種類、配合量を誤まると有機バインダー
中に金属粉末を均一に分散できなくなるばかりか、成形
用材料の流動性不足による射出成形不良、グリーン成形
体の著しい強度不足によって金型からの取出し及び次工
程までの移動、保存中に破損を生じたり、脱バインダー
時、成形品に亀裂、フクレ、変形等を生じたりする。さ
らに有機バインダーの熱安定性が悪い場合、射出成形時
にシリンダー内で有機バインダーの劣化が起こり、射出
不良となる。In injection molding of metal powder, it is very important to find the combination, blending ratio, and amount of organic binder that is suitable for the metal powder used.Thermoplastic resin, which is an essential component, is especially important, and its type, If the blending amount is incorrect, not only will it not be possible to uniformly disperse the metal powder in the organic binder, but also injection molding will be defective due to lack of fluidity of the molding material, and the green molded product will have a significant lack of strength, resulting in difficulty in ejecting it from the mold and waiting for the next process. This may cause damage during transportation or storage, or cracks, blisters, deformation, etc. may occur in the molded product when the binder is removed. Furthermore, if the thermal stability of the organic binder is poor, the organic binder will deteriorate within the cylinder during injection molding, resulting in poor injection.
「実施例」
実施例1
平均粒径7.41Lmを有するJIS−304ステンレ
ス鋼粉末100重h1部に対し、ポリスチレン1.96
重量部、ポリブチルメタクリレ−]・2.52重量部、
エチレン酢酸ヒニル共重合体1.12重量部、ワックス
として58℃の融点を有するパラフィンワックス4.4
重量部、可塑剤としてジブチルフタレート1重量部を加
圧ニグーで150℃で1時間加熱混練した後、混線物を
3X3X4mm程度のベレットにし、射出成形用材料と
する。"Example" Example 1 1.96 parts of polystyrene was added to 1 part by weight of JIS-304 stainless steel powder having an average particle size of 7.41 Lm.
parts by weight, polybutyl methacrylate]・2.52 parts by weight,
1.12 parts by weight of ethylene-hinyl acetate copolymer, 4.4 parts of paraffin wax having a melting point of 58°C as a wax
After heating and kneading 1 part by weight of dibutyl phthalate as a plasticizer at 150°C for 1 hour using a pressurizer, the mixed material is made into a pellet of about 3 x 3 x 4 mm and used as an injection molding material.
これを成形温度120〜160°C1射出圧力500−
1000kg/cm2の条件で高さ50mm、最大肉厚
5mmのJIS B−1176に定められたボルトを
成形する。The molding temperature is 120-160°C, the injection pressure is 500-
Bolts specified in JIS B-1176 with a height of 50 mm and a maximum wall thickness of 5 mm are formed under the conditions of 1000 kg/cm2.
得られた成形物をN2雰囲気中、室温から120°Cま
でを3時間で昇温し、120℃以上以降は、5〜b
し、同温度で2時間保持し、有機バインダーを加熱分解
、除去した後、1350°Cの温度で1時間真空焼成し
た。The temperature of the obtained molded product was raised from room temperature to 120°C over 3 hours in a N2 atmosphere, and after 120°C, the temperature was increased to 5 to 15°C, and the same temperature was maintained for 2 hours to thermally decompose and remove the organic binder. After that, vacuum baking was performed at a temperature of 1350°C for 1 hour.
得られた焼結体は、理論密度比95%のクラ−2り等の
欠陥のない良好な焼結体であった。The obtained sintered body was a good sintered body with a theoretical density ratio of 95% and no defects such as cracks.
実施例2゜
平均粒径14ILmを有するカーボニル・鉄粉100重
量部に対してポリスチレン1.82重量部、ポリブチル
メタクリレ−)2.08重量部、エチレン酢酸ビニル共
重合体1−3重量部、ワックスとして融点69℃を有す
るパラフィンワックス3.8重量部、潤滑剤としてステ
アリン酸1重是部を、加圧ニーグーで150℃で1時間
、加熱混練した後、実施例1と同様にボルトを成形、脱
バインダーする。これを還元性雰囲気中、1200°C
の温度で1時間焼結した。Example 2 1.82 parts by weight of polystyrene, 2.08 parts by weight of polybutyl methacrylate, 1-3 parts by weight of ethylene-vinyl acetate copolymer per 100 parts by weight of carbonyl iron powder having an average particle size of 14 ILm. After heating and kneading 3.8 parts by weight of paraffin wax having a melting point of 69°C as a wax and 1 part of stearic acid as a lubricant at 150°C for 1 hour using a pressurized knee gun, bolts were screwed in the same manner as in Example 1. Shape and remove binder. This was heated to 1200°C in a reducing atmosphere.
It was sintered at a temperature of 1 hour.
得られた焼結体は、理論密度比90%の欠陥のない良好
な焼結体であった。The obtained sintered body was a good sintered body without defects and had a theoretical density ratio of 90%.
実施例3゜
平均粒径32ILmを有するJIS拳316ステンレス
鋼粉末100重量部に対して、ポリスチレン1.55重
量部、ポリブチルメタクリレート3.15重量部、エチ
レン酢酸ビニル共重合体1.6重量部、ワックスとして
融点84℃のマイクロクリスタリンワックス5.2重量
部、可塑剤としてジブチルフタレート1重量部を用いる
以外は、実施例1と同様に加熱混線、成形、脱パイング
ー、焼結を行なった。Example 3: 1.55 parts by weight of polystyrene, 3.15 parts by weight of polybutyl methacrylate, and 1.6 parts by weight of ethylene-vinyl acetate copolymer for 100 parts by weight of JIS Fist 316 stainless steel powder having an average particle size of 32ILm. The heating, molding, depaining, and sintering were carried out in the same manner as in Example 1, except that 5.2 parts by weight of microcrystalline wax with a melting point of 84° C. was used as the wax and 1 part by weight of dibutyl phthalate was used as the plasticizer.
得られた焼結体は、理論密度比86%の全くクラック等
の欠陥のない良好な焼結体であった。The obtained sintered body was a good sintered body with a theoretical density ratio of 86% and no defects such as cracks.
比較例。Comparative example.
実施例1で使用した金属粉末100部に対して、ポリブ
チルメタクリレート1.74重量部、エチレン酢酸ビニ
ル共重合体4.06重量部、ポリエチレンワックス4.
2重量部、ステリン酸1重量部を、加圧ニーグーで14
0℃、1時間加熱混練し、成形温度130℃で実施例1
と同様のボルトを成形する。For 100 parts of the metal powder used in Example 1, 1.74 parts by weight of polybutyl methacrylate, 4.06 parts by weight of ethylene vinyl acetate copolymer, and 4.0 parts by weight of polyethylene wax.
2 parts by weight and 1 part by weight of steric acid in a pressurized knee gun for 14 hours.
Example 1 by heating and kneading at 0°C for 1 hour and molding temperature at 130°C.
Form a bolt similar to.
これをN2雰囲気中、室温から120℃までを3時間で
昇温し、120℃以降は、3℃/時間の昇温速度で45
0℃まで昇温し、同温度で2時間保持し脱バインダーを
行なったが、脱脂工程中、著しくフクレを生じ満足に脱
バインダーできなかった。This was heated in a N2 atmosphere from room temperature to 120°C in 3 hours, and after 120°C, the temperature was increased to 45°C at a heating rate of 3°C/hour.
The temperature was raised to 0° C. and the binder was removed by holding at the same temperature for 2 hours, but during the degreasing process, significant blistering occurred and the binder could not be removed satisfactorily.
「発明の効果」
本発明に従って得られる射出成形用金属粉末組成物を使
用すれば、従来と異なり、射出成形法によって複雑な形
状を有し、かつ高密度な金属焼結部材が工業的に製造可
能となり、当該技術分野に大きく寄与しうる。"Effects of the Invention" By using the metal powder composition for injection molding obtained according to the present invention, sintered metal parts with complex shapes and high density can be manufactured industrially by injection molding method, unlike conventional methods. This can greatly contribute to the technical field.
特許出願人 第一工業製薬株式会社Patent applicant Daiichi Kogyo Seiyaku Co., Ltd.
Claims (2)
用金属粉末組成物において、 有機バインダーが、ポリスチレン5〜30 重量%、ポリブチルメタクリレート5〜35重量%及び
エチレン酢酸ビニル共重合体5〜25重量%を必須成分
として含有することを特徴とする射出成形用金属粉末組
成物。(1) In a metal powder composition for injection molding in which 5 to 15 parts by weight of an organic binder is blended to 100 parts by weight of metal powder, the organic binders include 5 to 30 parts by weight of polystyrene and 5 to 35 parts by weight of polybutyl methacrylate. A metal powder composition for injection molding, characterized in that it contains 5 to 25% by weight of ethylene-vinyl acetate copolymer as an essential component.
することを特徴とする金属焼結部材の製造法。(2) A method for producing a metal sintered member, which comprises using the metal powder composition for injection molding according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18869488A JPH0617485B2 (en) | 1988-07-28 | 1988-07-28 | Metal powder composition for injection molding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18869488A JPH0617485B2 (en) | 1988-07-28 | 1988-07-28 | Metal powder composition for injection molding |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25007193A Division JPH0768567B2 (en) | 1993-09-10 | 1993-09-10 | Manufacturing method of sintered metal |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0238502A true JPH0238502A (en) | 1990-02-07 |
JPH0617485B2 JPH0617485B2 (en) | 1994-03-09 |
Family
ID=16228189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18869488A Expired - Lifetime JPH0617485B2 (en) | 1988-07-28 | 1988-07-28 | Metal powder composition for injection molding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0617485B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100574399B1 (en) * | 2004-10-25 | 2006-04-27 | 재단법인 포항산업과학연구원 | Water-soluble binder for powder injection molding |
-
1988
- 1988-07-28 JP JP18869488A patent/JPH0617485B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100574399B1 (en) * | 2004-10-25 | 2006-04-27 | 재단법인 포항산업과학연구원 | Water-soluble binder for powder injection molding |
Also Published As
Publication number | Publication date |
---|---|
JPH0617485B2 (en) | 1994-03-09 |
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