JPH0112801B2 - - Google Patents
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- Publication number
- JPH0112801B2 JPH0112801B2 JP56144188A JP14418881A JPH0112801B2 JP H0112801 B2 JPH0112801 B2 JP H0112801B2 JP 56144188 A JP56144188 A JP 56144188A JP 14418881 A JP14418881 A JP 14418881A JP H0112801 B2 JPH0112801 B2 JP H0112801B2
- Authority
- JP
- Japan
- Prior art keywords
- chamber
- sintering
- gas
- cooling
- temperature
- 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
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Powder Metallurgy (AREA)
- Tunnel Furnaces (AREA)
Description
本発明は、鉄系焼結部品の真空焼結にあたり、
生産性に優れ、しかも焼結温度の精度を上げるこ
とにより、焼結後の製品の寸法精度を良くするこ
とを特徴とする連続真空焼結炉に関するものであ
る。
鉄系焼結部品の焼結雰囲気としては、一般にブ
タン等の変成ガス、アンモニア分解ガス、N2ガ
スあるいはH2ガスが用いられているが、易酸化
性のCr等の元素を含む品物は、H2ガスを除いて
他の雰囲気では還元力が弱いため、品物が酸化し
やすいという問題があつた。
一方H2ガスの場合には、露点を低く管理すれ
ば品物の酸化は防げるが、他のガスに比べH2ガ
スのコストが高くつくという問題がある。
その点真空焼結は還元性が優れ、しかもガスを
使用しないで、エネルギー的にも非常に優利な方
法である。
しかしながら、従来の真空炉はバツチ式である
ため、製品を炉に挿入してから昇温―焼結温度で
の一定時間保持―冷却という過程をふみ、発熱体
が大気にふれても劣化しない温度まで低下しない
と、炉のフタを開けて製品を取り出せないという
問題があることから、サイクル時間が長く、通常
4〜5時間を要していた。このため大量生産を必
要とするような鉄系焼結機械部品には対処しにく
いという問題があり、対処できたとしても製品1
ケ当りの処理時間が長くなるということから、コ
ストが高くつくという問題があつた。
これを解消する手段として、最近連続的に処理
できる連続焼結炉が実用化されているが、発熱体
配置が側壁あるいは上下面のみの2面構造である
ため、炉内の温度バラツキが約20℃あり、そのた
め焼結後の品物の寸法バラツキが大きくなるとい
う問題がある。それに加えて、炉内におけるボー
ト処理が3〜4ケースとなつているため、1ボー
ト焼結室に挿入する毎に、N2ガスを導入して大
気圧にしてから、焼結室と予備室の中間扉を開け
る構造となつており、真空雰囲気がその都度中断
され、連続して雰囲気制御ができないという問題
を有している。これらの問題点を解決するために
考え出されたのが本発明による連続真空焼結炉で
ある。
以下本発明の実施例を図面に基づいて説明す
る。
第1図は本発明の焼結炉(以下本焼結炉と略
す)の概略を示したもので、1は脱ガス室で操業
時は500〜700℃の温度で保持されている。こゝで
脱ガス室1を設けた理由は、第1に中央の焼結室
2に品物を挿入する際に、焼結室の発熱体11が
大気にさらされて劣化することを防ぐための予備
室的な役目を果すこと、第2には真空焼結室2で
脱ガスを行うことは、成形体から出て来た潤滑材
が炉壁および真空ポンプ13内に一部付着し、雰
囲気の汚れ更にはポンプの性能低下をきたすた
め、前もつて脱ガスを行う方が望ましいこと、第
3には脱ガス室1と焼結室2とを連続化すること
により、脱ガス時に加熱された予熱を焼結時に有
効に生かせるため、焼結時の加熱に要するエネル
ギーがその分節約できるという点である。第1表
は焼結炉がバツチ式で脱ガスを別の炉で行うとい
う従来の方法と本焼結炉での加熱に要する電力エ
ネルギーを比較したもので、いずれも鉄系部品60
Kgを加熱した場合の数値である。これによつて本
焼結炉がエネルギーの節約という点でも、従来の
方法に比べ優れていることが判る。
The present invention relates to vacuum sintering of iron-based sintered parts.
The present invention relates to a continuous vacuum sintering furnace which is characterized by excellent productivity and which improves the dimensional accuracy of the sintered product by increasing the accuracy of the sintering temperature. The sintering atmosphere for iron-based sintered parts is generally a modified gas such as butane, ammonia decomposition gas, N 2 gas or H 2 gas, but for products containing easily oxidizable elements such as Cr, There was a problem that products were easily oxidized because the reducing power was weak in other atmospheres except H 2 gas. On the other hand, in the case of H 2 gas, oxidation of the product can be prevented by keeping the dew point low, but there is a problem in that H 2 gas is more expensive than other gases. In this respect, vacuum sintering has excellent reducing properties, does not use gas, and is an extremely advantageous method in terms of energy. However, since conventional vacuum furnaces are batch-type, the product is heated after being inserted into the furnace, held at the sintering temperature for a certain period of time, and then cooled down to a temperature at which the heating element does not deteriorate even when exposed to the atmosphere. Since there is a problem that the product cannot be taken out by opening the furnace lid unless the temperature has decreased to 100%, the cycle time is long and usually takes 4 to 5 hours. For this reason, there is a problem that it is difficult to deal with iron-based sintered machine parts that require mass production, and even if it could be solved, the product 1
There was a problem in that the cost was high because the processing time per piece was long. As a means to solve this problem, continuous sintering furnaces that can perform continuous processing have recently been put into practical use, but because the heating element is arranged in a two-sided structure with only the side walls or top and bottom surfaces, the temperature inside the furnace varies by about 20 degrees. ℃, and as a result, there is a problem that the dimensional variation of the products after sintering becomes large. In addition, since three to four cases of boat processing are carried out in the furnace, each time one boat is inserted into the sintering chamber, N2 gas is introduced to bring it to atmospheric pressure, and then the sintering chamber and preliminary chamber are The structure is such that the intermediate door of the vacuum chamber is opened, and the vacuum atmosphere is interrupted each time, resulting in the problem that continuous atmosphere control is not possible. The continuous vacuum sintering furnace of the present invention was devised to solve these problems. Embodiments of the present invention will be described below based on the drawings. FIG. 1 schematically shows the sintering furnace of the present invention (hereinafter referred to as the present sintering furnace), and 1 is a degassing chamber which is maintained at a temperature of 500 to 700° C. during operation. The reason for providing the degassing chamber 1 here is, firstly, to prevent the heating element 11 in the sintering chamber from being exposed to the atmosphere and deteriorating when an article is inserted into the central sintering chamber 2. The vacuum sintering chamber 2 functions as a preliminary chamber, and the second reason is that the vacuum sintering chamber 2 performs degassing. It is preferable to perform degassing beforehand to avoid contamination and deterioration of pump performance. Thirdly, by making the degassing chamber 1 and the sintering chamber 2 continuous, it is possible to avoid heating during degassing. This preheating can be used effectively during sintering, so the energy required for heating during sintering can be saved accordingly. Table 1 compares the electric energy required for heating in this sintering furnace with the conventional method in which the sintering furnace is a batch type and degassing is performed in a separate furnace.
This is the value when heating kg. This shows that the present sintering furnace is superior to conventional methods in terms of energy savings as well.
【表】
次に脱ガス室の温度を500〜700℃とした理由
は、500℃以下では成形体中に分散している潤滑
材の飛散が不十分であり、真空雰囲気における焼
結時に残つていた潤滑材が出てくるため、焼結雰
囲気の制御に悪影響を及ぼすという問題があるこ
と、一方700℃に達すると潤滑材は殆ど抜けてお
り、それ以上温度を上げても効果は変らないから
である。
次に脱ガスの雰囲気ガスについて述べる。
第1図の18は脱ガス雰囲気ガスの導入回路で
ある。雰囲気ガスとしてはN2ガス、アンモニア
分解ガス、H2ガス等非酸化性ガスであれば何で
もよいが、成形体から出て来る潤滑材は白煙とな
るので、出来ればアンモニア分解ガス、H2ガス
等の燃焼性ガスを使用して白煙を燃やして炉外に
排出させる方が環境対策の点で望ましい。
以上が本発明で雰囲気ガスとして燃焼性ガスを
用いる理由である。但し、アンモニア分解ガス
(N2+3H2)にN2ガスを混合して使用する場合に
は、混合後においてH2ガスの占める体積比が25
%以上となる様にN2ガス混合量を制限する必要
がある。その理由はH2ガスの体積比が25%以下
になると混合ガスとしては不燃性となり、潤滑材
を燃焼させることが出来なくなるからである。
具体的にはN2ガスを混合する際、その混合量
は全体に占める体積比で66%以下であることが必
要である。
以上アンモニア分解ガスとN2ガスとの混合ガ
スについて述べたが、混合ガスは最終的にはN2
ガスとH2ガスから成るので、アンモニア分解ガ
スの代りにH2ガスを用い、H2ガスとN2ガスの混
合ガスを用いることも可能である。この場合も当
然ながらH2ガス量は体積比で25%以上必要であ
る。
ボートの挿入であるが、挿入は入口の扉4を開
けて外部のローダーを用いて脱ガス室1のボート
21の位置にセツトする。扉4を開ける際には上
部の排気口8をフタ9によつて閉じておくと共
に、炉内圧は1気圧をやゝ上回る程度にして大気
からエアーをまき込まないようにする。ボート2
1がセツトされた後は扉4を閉めて排気口8のフ
タ9を開けて排気口8から潤滑材をガスと共に燃
焼させながら排出させる。脱ガス室に保持する時
間は次工程の焼結時間によつて決定されるが、潤
滑材を十分に飛散させるという点からは少なくと
も30分以上が望ましい。
次に焼結室への移動であるが、移動の前に先ず
焼結室内にガス導入回路19、電磁弁16から
N2ガスあるいはArガスを導入し、炉内圧を脱ガ
ス室と同等か若干上まわる程度にし、この状態で
中間扉5を開ける。次に脱ガス室内下部にセツト
されたローダーを用いてボートを焼結室内に移動
させ、セツトが終ると中間扉5を閉め、ガス導入
を止め、電磁弁14を開にし、真空ポンプ13で
炉内を真空にする。この間の所要時間はできる限
り短時間であることが望ましいので、ガス導入回
路19からのガス流量を多くなるようして、真空
ポンプの排気能力も高くして、大体5分以内で移
動完了できるようにすることが望ましい。
脱ガス室1から焼結室2へボート21を移動さ
せる別の方法として、脱ガス室に真空ポンプ1
3′、電磁弁14′による排気回路を設け、脱ガス
終了後、排気口8のフタを閉じ、真空ポンプ1
3′で炉内を真空にし、焼結室も真空にした状態
で中間扉5を開け、ボート21を移動させること
も可能である。この場合、焼結室のガス導入回路
19および電磁弁16は不要となる。
次に焼結室の発熱体の構造について述べる。従
来の焼結炉は発熱体の配置が側面あるいは上下面
の2面に限られているため、炉内の温度バラツキ
が大きく、ボートの中央部と端部との温度差が大
きくなり、通常温度巾で20℃位あり、そのため焼
結体の寸法バラツキも大きくなるという問題があ
つた。そこで本焼結体では温度精度を上げるた
め、第3図に示すような発熱体の構造をとるこ
とゝした。第3図でカーボン発熱体31(前部),
32(中央部),33(後部)は4面構造をなし
ており、それぞれ別個に電流回路35および電源
36によつて加熱されるようになつている。温度
制御は熱電対34によつて温度を検知し、マイコ
ン38およびフイードバツク回路37によつて、
所定の温度あるいは昇温速度を維持できるよう
に、発熱体31,32,33に加える電力を調整
することにより達成する。すなわち、上下方向の
温度バラツキは上下面の発熱体によつて低く抑
え、前後方向のバラツキは発熱体を3ゾーンに分
割制御することによつて低く抑えることができ、
極めて高い温度精度が得られることが可能となつ
た。第2表は1200℃の温度における炉内の温度バ
ラツキを示したものである。[Table] Next, the reason why the temperature of the degassing chamber was set to 500 to 700℃ is that below 500℃, the lubricant dispersed in the compact is not sufficiently dispersed, and the lubricant remaining during sintering in a vacuum atmosphere However, once the temperature reaches 700°C, most of the lubricant is gone, and the effect will not change even if the temperature is increased further. It is from. Next, the atmospheric gas for degassing will be described. Reference numeral 18 in FIG. 1 is a degassing atmosphere gas introduction circuit. Any non-oxidizing gas such as N 2 gas, ammonia decomposition gas, H 2 gas, etc. may be used as the atmospheric gas, but since the lubricant coming out of the molded product becomes white smoke, it is preferable to use ammonia decomposition gas, H 2 gas, etc. From an environmental standpoint, it is preferable to use combustible gas such as gas to burn the white smoke and discharge it outside the furnace. The above is the reason why a combustible gas is used as the atmospheric gas in the present invention. However, when using N 2 gas mixed with ammonia decomposition gas (N 2 + 3H 2 ), the volume ratio occupied by H 2 gas after mixing is 25%.
It is necessary to limit the amount of N 2 gas mixed so that it is at least %. The reason for this is that when the volume ratio of H 2 gas becomes 25% or less, the mixed gas becomes nonflammable and the lubricant cannot be burned. Specifically, when mixing N 2 gas, the mixing amount needs to be 66% or less by volume of the whole. The above description was about a mixed gas of ammonia decomposition gas and N2 gas, but the mixed gas ultimately becomes N2 gas .
Since it consists of gas and H 2 gas, it is also possible to use H 2 gas instead of ammonia decomposition gas, or to use a mixed gas of H 2 gas and N 2 gas. In this case, naturally, the amount of H 2 gas is required to be 25% or more by volume. The boat is inserted by opening the entrance door 4 and using an external loader to set the boat 21 in the degassing chamber 1. When opening the door 4, the upper exhaust port 8 is closed with a lid 9, and the pressure inside the furnace is kept slightly above 1 atm to prevent air from being drawn in from the atmosphere. boat 2
1 is set, the door 4 is closed, the lid 9 of the exhaust port 8 is opened, and the lubricant is discharged from the exhaust port 8 while being burned together with gas. The time for holding in the degassing chamber is determined by the sintering time of the next step, but from the viewpoint of sufficiently scattering the lubricant, it is preferably at least 30 minutes. Next, it is time to move to the sintering chamber, but before moving, first, the gas introduction circuit 19 and the solenoid valve 16 are connected to the sintering chamber.
N 2 gas or Ar gas is introduced to make the pressure inside the furnace equal to or slightly higher than that of the degassing chamber, and in this state, the intermediate door 5 is opened. Next, the boat is moved into the sintering chamber using a loader set at the bottom of the degassing chamber, and when the setting is completed, the intermediate door 5 is closed, the gas introduction is stopped, the solenoid valve 14 is opened, and the vacuum pump 13 is used to move the boat into the sintering chamber. Make a vacuum inside. It is desirable that the time required during this time be as short as possible, so the gas flow rate from the gas introduction circuit 19 is increased and the exhaust capacity of the vacuum pump is also increased so that the movement can be completed within approximately 5 minutes. It is desirable to do so. Another method for moving the boat 21 from the degassing chamber 1 to the sintering chamber 2 is to add a vacuum pump 1 to the degassing chamber.
3', an exhaust circuit is provided using a solenoid valve 14', and after the degassing is completed, the lid of the exhaust port 8 is closed, and the vacuum pump 1 is closed.
It is also possible to move the boat 21 by opening the intermediate door 5 with the furnace interior evacuated at 3' and the sintering chamber also evacuated. In this case, the gas introduction circuit 19 and the solenoid valve 16 of the sintering chamber become unnecessary. Next, the structure of the heating element in the sintering chamber will be described. In conventional sintering furnaces, the placement of heating elements is limited to the sides or the top and bottom surfaces, so the temperature inside the furnace varies widely, and the temperature difference between the center and the ends of the boat becomes large. The temperature was about 20°C in width, which caused the problem of large dimensional variations in the sintered bodies. Therefore, in order to improve the temperature accuracy of this sintered body, we adopted the structure of the heating element as shown in FIG. 3. In Fig. 3, carbon heating element 31 (front part),
32 (center) and 33 (rear) have a four-sided structure, and are heated separately by a current circuit 35 and a power source 36. Temperature control is performed by detecting the temperature using a thermocouple 34, and by using a microcomputer 38 and a feedback circuit 37.
This is achieved by adjusting the power applied to the heating elements 31, 32, and 33 so that a predetermined temperature or temperature increase rate can be maintained. In other words, temperature variations in the vertical direction can be kept low by the heating elements on the upper and lower surfaces, and variations in the longitudinal direction can be kept low by dividing and controlling the heating elements into three zones.
It has become possible to obtain extremely high temperature accuracy. Table 2 shows the temperature variation inside the furnace at a temperature of 1200°C.
【表】
次に焼結室における品物の保持時間について述
べる。脱ガス室で600℃に加熱された品物を1200
℃で焼結する場合を例にとると、昇温速度を20
℃/分とすれば、約30分で焼結温度に達する。こ
こで焼結温度での保持時間を30分とすれば、結局
焼結室での保持時間は60分となる。保持時間につ
いては昇温速度、焼結温度、焼結温度での保持時
間の設定によつて適宜変更が可能である。
最後に、焼結された品物の冷却室への移動であ
るが、この場合、冷却室も真空ポンプによつて炉
内を真空にし、その時点で中間扉6を開け、冷却
室に設けられたローダーによつて焼結室内のボー
トを取り出して冷却室にセツトする。セツト終了
後直ちに中間扉6を閉じ、ガス導入回路20、電
磁弁17により冷却ガスを炉内圧700〜760Torr
に達するまで導入する。この時冷却速度を早めた
い場合には、冷却ガスを導入した後、フアン12
をまわしてガスフアン強制冷却を実施する。ある
いはまた更に冷却速度を早めたい場合には、セツ
トされたボートをエレベーターによつて、冷却室
下部の油槽22に下げ油焼入れを実施する。油焼
入れが終ればエレベーターによつて元の位置に上
昇させ油切りを行う。冷却が終れば炉内圧を大気
圧とした後、出口の扉7を開け外部ローダーによ
つて炉内のボートを外へ出す。
上述のようなサイクルによつて、品物の脱ガ
ス、焼結および冷却を連続的に実施するのであ
る。たゞし、実際に連続的に操業する場合には、
ボートの移動先を先ず空にしておくという必要か
ら、先ず冷却室のボートを外へ、次に焼結室のボ
ートを冷却室へ、その次に脱ガス室のボートを焼
結室へと順次後のボートから先に移動させること
が必要である。
最後に、60Kgの製品を脱ガス、焼結および冷却
させるのに要する時間について、従来のバツチ式
の炉と本発明の焼結炉で行つた比較結果を第3表
に示す。第3表より、本焼結炉の生産性がバツチ
式の従来炉に比べ、格段に優れていることが明ら
かである。[Table] Next, the holding time of the items in the sintering chamber will be described. 1200 ℃ of goods heated to 600℃ in a degassing chamber
For example, when sintering at ℃, the temperature increase rate is set to 20
If the rate is °C/min, the sintering temperature will be reached in about 30 minutes. If the holding time at the sintering temperature is 30 minutes, the holding time in the sintering chamber will be 60 minutes. The holding time can be changed as appropriate by setting the heating rate, sintering temperature, and holding time at the sintering temperature. Finally, the sintered product is transferred to the cooling chamber. In this case, the cooling chamber is also evacuated by a vacuum pump, and at that point the intermediate door 6 is opened, and the The boat in the sintering chamber is taken out by a loader and set in the cooling chamber. Immediately after the setting is completed, close the intermediate door 6 and supply the cooling gas to the furnace pressure of 700 to 760 Torr using the gas introduction circuit 20 and solenoid valve 17.
Introduce until reaching . If you want to speed up the cooling rate at this time, after introducing the cooling gas,
Turn on the gas fan to perform forced cooling. Alternatively, if it is desired to further increase the cooling rate, the set boat is lowered into the oil tank 22 at the bottom of the cooling chamber using an elevator and oil quenching is performed. Once the oil quenching is complete, it is raised to its original position using an elevator and the oil is removed. When cooling is completed, the pressure inside the furnace is brought to atmospheric pressure, and then the exit door 7 is opened and the boat inside the furnace is taken out by an external loader. The cycles described above sequentially degas, sinter, and cool the article. However, when actually operating continuously,
Because of the need to empty the boats, first the boat in the cooling room was moved outside, then the boat in the sintering room was moved into the cooling room, and then the boat in the degassing room was moved into the sintering room. It is necessary to move the later boats first. Finally, Table 3 shows the comparison results between the conventional batch type furnace and the sintering furnace of the present invention regarding the time required to degas, sinter, and cool a 60 kg product. From Table 3, it is clear that the productivity of the present sintering furnace is much superior to that of the conventional batch-type furnace.
第1図は本発明の連続真空焼結炉の実施例概略
説明図、第2図は脱ガス―焼結に至る製品加熱に
要する電力エネルギーの温度パターン図でイは従
来の方法によるもの、ロは本焼結炉によるもの、
第3図は本焼結炉の温度精度を上げるための発熱
体の構造を示すものである。
1…脱ガス室、2…焼結室、3…冷却室、4…
入口扉、5,6…中間扉、7…出口扉、8…潤滑
材とガスの排気口、9…排気口フタ、10…断熱
材、11…発熱体、12…冷却用フアン、13,
13′…真空ポンプ、14,14′,15,16,
17…電磁弁、18,19,20…ガス導入回
路、21…ボート、22…油槽、31,32,3
3…カーボン発熱体、34…熱電対、35…発熱
体加熱用電源回路、36…発熱体電源、37…フ
イードバツク回路(温度制御、電力制御信号回
路)、38…マイコン。
Fig. 1 is a schematic explanatory diagram of an embodiment of the continuous vacuum sintering furnace of the present invention, Fig. 2 is a temperature pattern diagram of the electrical energy required to heat the product from degassing to sintering, and A is a diagram of the conventional method; is produced by this sintering furnace,
FIG. 3 shows the structure of a heating element for improving the temperature accuracy of this sintering furnace. 1... Degassing chamber, 2... Sintering chamber, 3... Cooling chamber, 4...
Entrance door, 5, 6... Intermediate door, 7... Exit door, 8... Lubricant and gas exhaust port, 9... Exhaust port cover, 10... Heat insulating material, 11... Heating element, 12... Cooling fan, 13,
13'...Vacuum pump, 14, 14', 15, 16,
17... Solenoid valve, 18, 19, 20... Gas introduction circuit, 21... Boat, 22... Oil tank, 31, 32, 3
3...Carbon heating element, 34...Thermocouple, 35...Power supply circuit for heating the heating element, 36...Heating element power supply, 37...Feedback circuit (temperature control, power control signal circuit), 38...Microcomputer.
Claims (1)
空雰囲気中で焼結させる焼結炉において、その構
造が成形時の金型潤滑を目的として、原料粉末中
に添加混合された潤滑材を加熱して成形体から飛
散させ、さらに飛散した潤滑材を燃焼ガスにより
燃焼させて排出する機構を設けた脱ガス室と、脱
ガスされた成形体を真空雰囲気中で焼結させる焼
結室および焼結された製品を非酸化性雰囲気ガス
中で冷却させる冷却室からなり、品物挿入側から
脱ガス室→焼結室→冷却室の順に連続して配置さ
れ、各室の間には中間扉を設けることにより、各
各独立して気密性を保つことが出来る構造を有す
ることを特徴とする連続真空焼結炉。 2 焼結室における発熱体の配置を上下面および
左右の側壁の四面とすると共に、ボート移動方向
に発熱体を3分割し、それぞれ別個に温度制御が
出来るようにしたことを特徴とする特許請求の範
囲第1項記載の連続真空焼結炉。 3 冷却室に冷却用の非酸化性ガスを導入させる
ガス導入回路、および冷却室の上部に少なくとも
1台以上のフアンを設けると共に、冷却室の下部
には油槽を設け、エレベーターにより製品の油槽
への出し入れが出来る装置を設けたことを特徴と
する特許請求の範囲第1項または第2項記載の連
続真空焼結炉。[Scope of Claims] 1. In a sintering furnace in which a compact formed by powder metallurgy is sintered in a vacuum atmosphere, the structure is such that it is added to the raw material powder for the purpose of mold lubrication during molding. A degassing chamber is equipped with a mechanism that heats the mixed lubricant and scatters it from the compact, then burns and discharges the scattered lubricant with combustion gas, and burns the degassed compact in a vacuum atmosphere. It consists of a sintering chamber for sintering and a cooling chamber for cooling the sintered product in a non-oxidizing atmosphere gas.The chambers are successively arranged in the order of degassing chamber → sintering chamber → cooling chamber from the product insertion side. A continuous vacuum sintering furnace characterized by having a structure in which airtightness can be maintained independently of each other by providing an intermediate door between them. 2. A patent claim characterized in that the heating elements in the sintering chamber are arranged on four sides: the upper and lower surfaces and the left and right side walls, and the heating elements are divided into three parts in the direction of movement of the boat, so that the temperature can be controlled separately for each part. The continuous vacuum sintering furnace according to item 1. 3. A gas introduction circuit for introducing non-oxidizing gas for cooling into the cooling chamber, and at least one or more fans in the upper part of the cooling chamber, and an oil tank in the lower part of the cooling chamber, and an elevator to transport the product to the oil tank. 3. A continuous vacuum sintering furnace according to claim 1 or 2, further comprising a device that can take in and out.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14418881A JPS5845304A (en) | 1981-09-11 | 1981-09-11 | Continuous vacuum sintering furnace |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14418881A JPS5845304A (en) | 1981-09-11 | 1981-09-11 | Continuous vacuum sintering furnace |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5845304A JPS5845304A (en) | 1983-03-16 |
| JPH0112801B2 true JPH0112801B2 (en) | 1989-03-02 |
Family
ID=15356245
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14418881A Granted JPS5845304A (en) | 1981-09-11 | 1981-09-11 | Continuous vacuum sintering furnace |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5845304A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5861424U (en) * | 1981-10-22 | 1983-04-25 | 東北金属工業株式会社 | vacuum sintering equipment |
| JPS609801A (en) * | 1983-06-27 | 1985-01-18 | Chugai Ro Kogyo Kaisha Ltd | Vacuum sintering furnace |
| JPS60164448A (en) * | 1984-02-08 | 1985-08-27 | Hideike:Kk | Device for separating rice bran from embryo bud |
| JPS61291081A (en) * | 1985-06-18 | 1986-12-20 | 株式会社 サタケ | Method and apparatus for sorting germ from rice rough bran |
| JPH0311028U (en) * | 1989-06-21 | 1991-02-01 | ||
| JP4783032B2 (en) * | 2004-02-18 | 2011-09-28 | 住友電工焼結合金株式会社 | Sintered high speed steel, its manufacturing method and sliding parts made of the sintered high speed steel |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS587059B2 (en) * | 1974-09-05 | 1983-02-08 | ソニー株式会社 | Hakumaku No Tokusei Kensahou |
| JPS5214312U (en) * | 1975-07-18 | 1977-02-01 | ||
| JPS542643A (en) * | 1977-06-08 | 1979-01-10 | Japan Radio Co Ltd | Hybrid calculator |
| JPS5435805A (en) * | 1977-08-26 | 1979-03-16 | Honda Motor Co Ltd | Method of producing ferrous powder sintered body |
| JPS5468706A (en) * | 1977-11-11 | 1979-06-02 | Ricoh Co Ltd | Preparation of sintered product |
| JPS5822077Y2 (en) * | 1979-06-12 | 1983-05-11 | 東海高熱工業株式会社 | High temperature high purity gas atmosphere furnace |
-
1981
- 1981-09-11 JP JP14418881A patent/JPS5845304A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5845304A (en) | 1983-03-16 |
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