JPH03260591A - Continuous sintering furnace - Google Patents
Continuous sintering furnaceInfo
- Publication number
- JPH03260591A JPH03260591A JP5752090A JP5752090A JPH03260591A JP H03260591 A JPH03260591 A JP H03260591A JP 5752090 A JP5752090 A JP 5752090A JP 5752090 A JP5752090 A JP 5752090A JP H03260591 A JPH03260591 A JP H03260591A
- Authority
- JP
- Japan
- Prior art keywords
- zone
- furnace
- sintering
- furnace wall
- degreasing
- 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
Links
- 238000005245 sintering Methods 0.000 title claims abstract description 47
- 238000005238 degreasing Methods 0.000 claims abstract description 25
- 239000011230 binding agent Substances 0.000 claims abstract description 15
- 238000001816 cooling Methods 0.000 claims abstract description 15
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000956 alloy Substances 0.000 claims abstract description 13
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 13
- 239000011819 refractory material Substances 0.000 claims abstract description 11
- 239000000919 ceramic Substances 0.000 claims description 21
- 239000000126 substance Substances 0.000 claims description 7
- 239000010935 stainless steel Substances 0.000 claims description 5
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 3
- 238000009413 insulation Methods 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 230000002787 reinforcement Effects 0.000 abstract description 2
- 230000035515 penetration Effects 0.000 abstract 1
- 230000008961 swelling Effects 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 description 12
- 239000000843 powder Substances 0.000 description 7
- 238000009423 ventilation Methods 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000004570 mortar (masonry) Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000007606 doctor blade method Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 229910052878 cordierite Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000007569 slipcasting Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Landscapes
- Tunnel Furnaces (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、焼結性セラミックス粉末と有機質バインダー
との混合物を成形したグリーン体を連続して脱脂、焼結
する連続焼結炉に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a continuous sintering furnace for continuously degreasing and sintering a green body formed from a mixture of sinterable ceramic powder and an organic binder.
セラミ、クス焼結体の成形品を製造するには、焼結性セ
ラミクラス粉末と有機質とを主体とする混合物を、粉末
プレス法、ドクターブレード法、押出法、射出成形法、
スリップキャスト法などで各種形状のセラミックスグリ
ーン体をつくり、これをパッチ式、或いは連続式の焼結
炉によって焼結している。In order to produce molded products of ceramic and sintered bodies, a mixture mainly consisting of sinterable ceramic class powder and an organic substance is prepared using a powder pressing method, a doctor blade method, an extrusion method, an injection molding method,
Ceramic green bodies of various shapes are made by slip casting, etc., and then sintered in a patch-type or continuous-type sintering furnace.
バッチ式焼結炉を用いた場合、被焼結物の量が多くなる
と、炉内への搬入、搬出に人手を要し効率が悪いため、
電子部品や自動車部品などの工業部品のように多量の焼
結体を生産するには、効率よく脱脂、焼結することが出
来る内壁がアルミナ質耐火物でつくられた連続焼結炉が
用いられる。When using a batch-type sintering furnace, if the amount of material to be sintered increases, it will require manpower to carry it into and out of the furnace, resulting in poor efficiency.
To produce large quantities of sintered bodies such as industrial parts such as electronic parts and automobile parts, a continuous sintering furnace whose inner wall is made of alumina refractory is used to efficiently degrease and sinter the furnace. .
連続焼結炉によって焼結する場合には、各種方法によっ
て成形されたセラミックスグリーン体を、アルミナ質や
シリカ質によって造られた板状セ。When sintering in a continuous sintering furnace, a ceramic green body formed by various methods is sintered into a plate-shaped body made of alumina or silica.
り上に載置し、これをこう鉢にそれぞれ収納する。Place them on top of each other and store them in their respective bowls.
これらこう鉢を多段に積重ね、この積重ねたものを炉の
入口において、ブツシャ−によって押して、一つづつ炉
内に送り込んで、連続焼結炉内に敷設されたレール上を
移動せしめ、脱脂ゾーン、焼結ゾーンにおいて、それぞ
れの温度で加熱焼結した後、冷却ゾーンで冷却する方法
が行われている。These pots are stacked in multiple stages, and the stack is pushed by a pusher at the entrance of the furnace, fed into the furnace one by one, and moved on the rails laid in the continuous sintering furnace, and is moved to the degreasing zone, In the sintering zone, a method is used in which the materials are heated and sintered at respective temperatures and then cooled in a cooling zone.
しかしながら、スチレン系、アクリル系、ワックス系、
プロピレン系オリゴマー等の熱可塑性有機物質をバイン
ダーとし、セラミックス粉末と混合して成形されたセラ
ミックスグリーン体を連続焼結炉を用いて脱脂、焼結し
た場合、グリーン体中にバインダーとして用いた有機質
が大量に台材されているため、脱脂ゾーンでは、炉壁に
有機質分解物が大量に付着する。この付着物は、炉壁土
部などから溶融滴下するとともに、脱脂ゾーンの排気孔
に分解物が堆積し、継目などから洩れ出すという問題が
あった。However, styrene-based, acrylic-based, wax-based,
When a ceramic green body is formed by mixing a thermoplastic organic substance such as a propylene oligomer with ceramic powder as a binder and is degreased and sintered using a continuous sintering furnace, the organic substance used as a binder is contained in the green body. Since a large amount of table material is used, a large amount of organic decomposition products adheres to the furnace walls in the degreasing zone. There was a problem in that this deposit melted and dripped from the furnace wall soil, etc., and decomposition products accumulated in the exhaust hole of the degreasing zone and leaked out from the joints and the like.
また、炉壁材として使用されているアルミナ質耐火材の
表面に付着した有機質分解物はタール状物質であるため
、定期的な清掃時においても除去が困難で、さらに、レ
ール上に滴下すると、レール上を移動するこう鉢を積重
ねたものがスムースに移動されなくなる欠点を生ずる。In addition, organic decomposition products that adhere to the surface of the alumina refractory material used as furnace wall materials are tar-like substances that are difficult to remove even during regular cleaning, and furthermore, if they drip onto the rails, This has the disadvantage that stacked pots that move on rails cannot be moved smoothly.
本発明は上記の事情に鑑みてなされたもので、上記セラ
ミックスグリーン体を連続焼結炉によって脱脂、焼結す
る場合、セラミックスグリーン体から発生する有機物質
分解物によって汚染された炉壁の清掃を容昌にし、かつ
、レール上に有機物質の分解物が滴下してこう鉢を積重
ねたものの移動がスムースに行なわれなくなることのな
い、連続焼結炉を提供することを目的とする。The present invention has been made in view of the above circumstances, and when the ceramic green body is degreased and sintered in a continuous sintering furnace, cleaning of the furnace wall contaminated by organic substance decomposition products generated from the ceramic green body is carried out. To provide a continuous sintering furnace which is large in capacity and does not cause decomposition products of organic substances to drip onto rails and prevent smooth movement of stacked pots.
本発明の連続焼結炉においては、
脱脂ゾーンの最内面を構成する炉壁材としてステンレス
質の耐熱金属板を用い、焼結ゾーンおよび冷却ゾーンの
炉壁材としてアルミナ質からなる耐火材を用いることを
解決手段とした。In the continuous sintering furnace of the present invention, a stainless steel heat-resistant metal plate is used as the furnace wall material constituting the innermost surface of the degreasing zone, and a refractory material made of alumina is used as the furnace wall material of the sintering zone and the cooling zone. This was the solution.
第1図は、本発明に係るトンネル状の連続焼結炉lの一
実施例を示す縦断面図で、入口1aから出口1bに向か
って、脱脂ゾーン2、焼結ゾーン3、冷却ゾーン4が順
次形成されいる。FIG. 1 is a longitudinal sectional view showing an embodiment of a tunnel-shaped continuous sintering furnace l according to the present invention, in which a degreasing zone 2, a sintering zone 3, and a cooling zone 4 are arranged from the inlet 1a toward the outlet 1b. Formed sequentially.
連続焼結炉l内部には、セラミックスグリーン体を収納
し、多段に積重ねたこう鉢(図示せず)を、順次プッシ
ャー5によって押して移動させるレール6が入口1aか
ら出口lbにわたって敷設されている。Inside the continuous sintering furnace 1, rails 6 are laid from the inlet 1a to the outlet 1b, which accommodate ceramic green bodies and move pots (not shown) stacked in multiple stages by pushing them one by one with a pusher 5.
上記脱脂ゾーン2は、第2図に横断面図を示すように、
最内面を構成する炉壁材として、ステンレス質の耐食、
耐熱合金板7が取付けられ、合金板7の外側には、断熱
、補強のためのアルミナ質耐火材8が設けられている。The degreasing zone 2, as shown in the cross-sectional view in FIG.
Corrosion-resistant stainless steel is used as the furnace wall material that makes up the innermost surface.
A heat-resistant alloy plate 7 is attached, and an alumina refractory material 8 is provided on the outside of the alloy plate 7 for heat insulation and reinforcement.
上記合金板7は、付着した有機質分解物の滴下を防止し
、分解物が側面を伝わって流下するように先端がやや尖
ったアーチ状に形成されている。The alloy plate 7 is formed in an arch shape with a slightly pointed tip to prevent attached organic decomposition products from dripping and to allow the decomposition products to flow down along the sides.
また合金板の両側外側には焼結ゾーン3から高温の空気
を送風し、炉内温度を保持するための通風孔9が設けら
れている。この通風孔9は脱脂ゾーン2の上部および下
部にも形成することが出来るが、この場合有機質分解物
の滴下に対する対策が必要となる。Further, ventilation holes 9 are provided on both outer sides of the alloy plate for blowing high-temperature air from the sintering zone 3 to maintain the temperature inside the furnace. The ventilation holes 9 can also be formed in the upper and lower parts of the degreasing zone 2, but in this case, measures against dripping of organic decomposition products are required.
上記合金板の側方外側には内部加熱用の電熱ヒータ10
が設けられている。この電熱ヒータ10の代りに通風孔
9にバーナを取付けて炉内を加熱することも可能である
。An electric heater 10 for internal heating is provided on the outer side of the alloy plate.
is provided. It is also possible to heat the inside of the furnace by attaching a burner to the ventilation hole 9 instead of the electric heater 10.
焼結ゾーン3は、第3図に横断面図を示すように、炉壁
は、従来のものと同様、アルミナ質耐火材8によってつ
くられている。また内部を加熱するには電熱ヒータlO
′および/または、通風孔9′に取付けられたバーナ1
1が用いられる。As shown in the cross-sectional view of FIG. 3, the sintering zone 3 has a furnace wall made of an alumina refractory material 8, as in the conventional furnace. Also, to heat the inside, use an electric heater lO
' and/or burner 1 installed in the ventilation hole 9'
1 is used.
冷却ゾーン4は第4図に示すように、内面を構成する材
料としては、従来のものと同様アルミナ質の耐火材が用
いられる。また廃熱を回収して脱脂ゾーン2の補助熱源
とするため通風孔9′を設けてもよい。As shown in FIG. 4, the cooling zone 4 uses an alumina refractory material as the material constituting the inner surface, as in the conventional cooling zone. Further, ventilation holes 9' may be provided to recover waste heat and use it as an auxiliary heat source for the degreasing zone 2.
また、使用されるセラミックスとしては、融点、分解温
度が800″C以上であり、tooo°C以上が好まし
く、特に1400℃以上の物が好適である。融点、分解
温度、または昇華温度が800″C未満では、脱脂時に
変形やふくれが生じる。Furthermore, the ceramics used have a melting point or decomposition temperature of 800°C or higher, preferably 1400°C or higher, and particularly preferably 1400°C or higher.A melting point, decomposition temperature, or sublimation temperature of 800°C or higher is preferable. If it is less than C, deformation or blistering occurs during degreasing.
使用されるセラミックスとしては、例えば、アルミナ、
シリカ、炭化けい素、窒化ケイ素、ジルコニア、コージ
ライト、窒化アルミニウム等があげられる。さらに焼結
助剤として、ホウ素、ベリリウム、炭素、酸化イツトリ
ウム、酸化セリウム、酸化マグネシウム、酸化リチウム
などを少量添加してもよい。この焼結助剤の添加量は、
通常セラミックス100重量部に対して20重量部以下
である。Examples of ceramics used include alumina,
Examples include silica, silicon carbide, silicon nitride, zirconia, cordierite, and aluminum nitride. Furthermore, a small amount of boron, beryllium, carbon, yttrium oxide, cerium oxide, magnesium oxide, lithium oxide, etc. may be added as a sintering aid. The amount of this sintering aid added is
Usually, the amount is 20 parts by weight or less per 100 parts by weight of the ceramic.
上記セラミックスの粒度は、平均粒径が0. 1〜20
0μmのものが用いられるが、0.1〜150μmのも
のが好ましく、特に0.1〜100μmのものが好適で
ある。平均粒径が0.1μm未満では、混練する際、均
一分散が困難であり、200μmを越えると、焼結の際
の保形性が悪くなると共に、焼結後の密度が小さくなり
、その機械的強度が低下する。The particle size of the above ceramics has an average particle size of 0. 1-20
A thickness of 0 μm is used, but a thickness of 0.1 to 150 μm is preferred, and a thickness of 0.1 to 100 μm is particularly preferred. If the average particle size is less than 0.1 μm, uniform dispersion is difficult during kneading, and if it exceeds 200 μm, shape retention during sintering will be poor and the density after sintering will be low, making it difficult to use the machine. target strength decreases.
また、バインダーとしては、エチレン系重合体、スチレ
ン系重合体、プロピレン系重合体エチレン−酢酸ビニル
共重合体、アルキル(炭素数6以下)メタアクリレート
を主成分(50w t%以上)とする共重合体く例えば
、ポリメチルメタアクリレート、ポリエチルメタアクリ
レート、ポリブチルメタアクリレート)、アルキル(炭
素数6以下)アクリレートを主成分(5Qw t%以上
)とする共重合体(例えば、ポリメチルアクリレート、
ポリエチルアクリレート、ポリブチルアクリレート)が
あげられる。但し、「系重合体」とは、該モノマーの単
独重合体、及びモノマーを主成分(少なくとも50wt
%)とした、他のモノマーとの共重合体を意味する。こ
れら合成樹脂バインダーの数平均分装置〔蒸気圧浸透法
(vapor pressure osmomet
er)によって測定〕は、通常2000−50万、特ニ
4000−50万が好ましい。In addition, binders include ethylene polymers, styrene polymers, propylene polymers, ethylene-vinyl acetate copolymers, and copolymers whose main component is alkyl (carbon number 6 or less) methacrylate (50wt% or more). For example, polymethyl methacrylate, polyethyl methacrylate, polybutyl methacrylate), copolymers containing alkyl (carbon number 6 or less) acrylate as a main component (5 Qw t% or more) (for example, polymethyl acrylate,
polyethyl acrylate, polybutyl acrylate). However, "system polymer" refers to a homopolymer of the monomer, and a monopolymer containing the monomer as the main component (at least 50 wt.
%) and means a copolymer with other monomers. A number-average device for these synthetic resin binders [vapor pressure osmomet method]
er)] is usually 2,000-500,000, preferably 4,000-500,000.
上記セラミックスおよびバイダーを用いてグリーン体を
成形するには、セラミックス粉末とバインターとを所定
の割合(通常セラミックスの粉末100重量部に対して
バインダーを5〜40重量部)で混合し、粉末プレス法
、ドクターブレード法、或いはペレット状とした後射出
成形法等によってセラミックスグリーン体を成形する。In order to mold a green body using the above ceramics and binder, ceramic powder and binder are mixed in a predetermined ratio (usually 5 to 40 parts by weight of binder to 100 parts by weight of ceramic powder), and a powder pressing method is used. A ceramic green body is molded by a doctor blade method, or an injection molding method after forming into pellets.
これらセラミックスグリーン体を連続焼結炉1によって
焼結するには、多数のグリーン体をこう鉢に入れ、さら
に多段に積重ね、これを入口より連続焼結炉内にブツシ
ャ−5を用いて一個ずつ押込んで、出口1b方向にむか
って一定速度で移動させ脱脂ゾーン2、焼結ゾーン3、
冷却ゾーン4を通過せしめる。In order to sinter these ceramic green bodies in the continuous sintering furnace 1, a large number of green bodies are placed in a mortar, further stacked in multiple stages, and then placed one by one into the continuous sintering furnace from the entrance using a busher 5. The degreasing zone 2, sintering zone 3,
It is made to pass through the cooling zone 4.
この際脱脂シー72の温度は300〜600 ’C特に
300〜500℃が好ましい。温度が600℃を越える
と、合金板が劣化し、また300′c未満では、脱脂体
の残存バインダーの量が多くなり焼結ゾーンにおいてふ
くれやクラックが発生する。At this time, the temperature of the degreasing sheath 72 is preferably 300-600'C, particularly 300-500'C. If the temperature exceeds 600°C, the alloy plate will deteriorate, and if the temperature is less than 300'C, the amount of residual binder in the degreased body will increase, causing blisters and cracks in the sintering zone.
焼結ゾーン3の温度は、それぞれ使用するセラミックス
の種類によって異なり、700〜1800°Cの範囲の
温度が用いられる。The temperature of the sintering zone 3 varies depending on the type of ceramic used, and is in the range of 700 to 1800°C.
また、連続焼結炉の長さは、10〜30mで、脱脂ゾー
ン、焼結ゾーン、冷却ゾーンの長さの割合は、70:2
0:10〜50 : 25 : 25の範囲である。ま
た、ブツシャ−によって押される、積重ねられたこう鉢
の移動速度は、0.25〜2m/時、特に0.25〜1
m/時が好ましい。速度が2m/時を越えると、焼結体
に有害な変形や、ふくれ、クラックが発生する。また速
度が0. 25m/時未満では、焼結に時間を要し経済
性を失なう。In addition, the length of the continuous sintering furnace is 10 to 30 m, and the ratio of the lengths of the degreasing zone, sintering zone, and cooling zone is 70:2.
The range is from 0:10 to 50:25:25. In addition, the moving speed of the stacked pots pushed by the butcher is 0.25 to 2 m/hour, especially 0.25 to 1 m/hour.
m/hour is preferred. If the speed exceeds 2 m/hour, harmful deformation, blistering, and cracking will occur in the sintered body. Also, the speed is 0. If the speed is less than 25 m/hour, sintering takes time and economical efficiency is lost.
上記ブツシャ−5により移動されるこう鉢中のグリーン
体は、脱脂ゾーンにおいて含有するバインターが熱分解
されて揮散する。The binder contained in the green bodies in the mortar moved by the bushier 5 is thermally decomposed and volatilized in the degreasing zone.
この揮散されたバインダーの熱分解物は炉壁に付着する
が、脱脂ゾーンの炉壁はステンレス質の耐食、耐熱合金
板7によって形成されているので、付着物は壁面に沿っ
て下方に流下し、壁面に浸透したり、壁面を膨潤させた
りすることがない。さらに定期点検時に壁面の付着物を
除去することは容易であり、炉内を一定の条件に保持す
ることが出来る。脱脂されたグリーン体は焼結ゾーンに
おいて焼結され冷却ゾーンで冷却されるが、バインダー
の揮散は、脱脂ゾーンで行われるので、焼結ゾーン、冷
却ゾーンではバインダーの揮散はたく、炉壁材として、
従来のアルミナ質耐火物が用いられる。The thermal decomposition products of the volatilized binder adhere to the furnace wall, but since the furnace wall in the degreasing zone is made of a stainless steel corrosion-resistant and heat-resistant alloy plate 7, the deposits flow downward along the wall surface. , will not penetrate or swell the wall surface. Furthermore, it is easy to remove deposits from the walls during periodic inspections, and the inside of the furnace can be maintained under constant conditions. The degreased green body is sintered in the sintering zone and cooled in the cooling zone, but the binder is volatilized in the degreasing zone. ,
Conventional alumina refractories are used.
以上述べたように、本発明の連続焼結炉は、殆ど全部の
有機質バインダーが揮散される脱脂ゾーンの内面が、ス
テンレス質よりなる耐食、耐熱性の合金板によって形成
されているので、付着した有機質分解物は、流下除去さ
れ、清掃も容易である。また、焼結ゾーン、冷却ゾーン
の内面はアルミナ質の耐火物によって形成されているが
、有機質分解物は脱脂ゾーンで揮散されているので、焼
結ゾーン、冷却ゾーンにおける揮散は殆どないので、付
着物が付着することもない。そのため連続焼結炉の内面
は、はぼ定常に保持され、炉の温度調整が行い易く、さ
らにレール上に分解物が滴下しない。したがって炉を移
動するこう鉢の移動速度が一定速度に維持され、製品に
むらを生ずることなく品質の管理が容易になる等の多く
の長所を有する。As described above, in the continuous sintering furnace of the present invention, the inner surface of the degreasing zone where almost all the organic binder is volatilized is formed of a corrosion-resistant and heat-resistant alloy plate made of stainless steel. Organic decomposition products are removed by flowing down and cleaning is easy. In addition, although the inner surfaces of the sintering zone and cooling zone are made of alumina refractories, organic decomposition products are volatilized in the degreasing zone, so there is almost no volatilization in the sintering zone and cooling zone. Kimono will not stick to it. Therefore, the inner surface of the continuous sintering furnace is kept almost constant, the temperature of the furnace can be easily adjusted, and decomposed products do not drip onto the rails. Therefore, the moving speed of the mortar moving through the furnace is maintained at a constant speed, and there are many advantages such as ease of quality control without causing unevenness in the product.
第1図は、本発明の連続焼結炉の一実施例を示す縦断面
図、第2図は、第1図の■−■線矢視断面図、第3図は
、第1図のm−■線矢視断面図、第4図は第1図の■−
■線矢視断面図である。
1・・・・・・連続焼結炉。1a・・・・・・入口、l
b・・・・・・出口、2・・・・・・脱脂ゾーン、3・
・・・・・焼結ゾーン、4・・・・・・冷却ゾーン、5
・・・・・・ブツシャ−6・・・・・・レール、7・・
・・・・合金板、8・・・・・・アルミナ質耐火材、9
・9′ ・9′・・・・・・通風孔、10・10′・・
・・・・電熱ヒータ、11・・・・・・バーナ。FIG. 1 is a longitudinal sectional view showing one embodiment of the continuous sintering furnace of the present invention, FIG. 2 is a sectional view taken along the line ■-■ in FIG. −■ Cross-sectional view taken along the line, Figure 4 is the ■− of Figure 1.
■It is a sectional view taken along the line. 1... Continuous sintering furnace. 1a... Entrance, l
b...Outlet, 2...Degreasing zone, 3.
... Sintering zone, 4 ... Cooling zone, 5
...Butsusha-6...Rail, 7...
...Alloy plate, 8...Alumina refractory material, 9
・9'・9'・・・Ventilation hole, 10・10'...
...Electric heater, 11...Burner.
Claims (1)
らなる混合物を成形したグリーン体を、脱脂ゾーン、焼
結ゾーンおよび冷却ゾーンを順次通して脱脂、焼結する
連続焼結炉において、脱脂ゾーンの最内面を構成する炉
壁材としてステンレス質の耐熱合金板を用い、焼結ゾー
ンおよび冷却ゾーンの炉壁材としてアルミナ質よりなる
耐火材を用いることを特徴とする連続焼結炉。In a continuous sintering furnace, a green body formed from a mixture of a binder mainly composed of organic substances and ceramics is passed through a degreasing zone, a sintering zone, and a cooling zone to degrease and sinter it. A continuous sintering furnace characterized in that a stainless steel heat-resistant alloy plate is used as the furnace wall material constituting the furnace wall, and a refractory material made of alumina is used as the furnace wall material in the sintering zone and the cooling zone.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5752090A JPH03260591A (en) | 1990-03-08 | 1990-03-08 | Continuous sintering furnace |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5752090A JPH03260591A (en) | 1990-03-08 | 1990-03-08 | Continuous sintering furnace |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03260591A true JPH03260591A (en) | 1991-11-20 |
Family
ID=13058013
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5752090A Pending JPH03260591A (en) | 1990-03-08 | 1990-03-08 | Continuous sintering furnace |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03260591A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0869191A3 (en) * | 1997-03-28 | 2000-10-04 | Ieco S.r.l. | Muffle for heat treating furnace |
| WO2013105578A1 (en) * | 2012-01-12 | 2013-07-18 | 住友化学株式会社 | Tunnel kiln and method for producing fired body using same |
| US20230051729A1 (en) * | 2018-05-23 | 2023-02-16 | Molecule Works Inc. | Process and Apparatus for Continuous Production of Porous Structures |
-
1990
- 1990-03-08 JP JP5752090A patent/JPH03260591A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0869191A3 (en) * | 1997-03-28 | 2000-10-04 | Ieco S.r.l. | Muffle for heat treating furnace |
| WO2013105578A1 (en) * | 2012-01-12 | 2013-07-18 | 住友化学株式会社 | Tunnel kiln and method for producing fired body using same |
| JP2013142526A (en) * | 2012-01-12 | 2013-07-22 | Sumitomo Chemical Co Ltd | Tunnel kiln and method of manufacturing sintered body using the same |
| US20230051729A1 (en) * | 2018-05-23 | 2023-02-16 | Molecule Works Inc. | Process and Apparatus for Continuous Production of Porous Structures |
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