JPH0464281B2 - - Google Patents
Info
- Publication number
- JPH0464281B2 JPH0464281B2 JP60243953A JP24395385A JPH0464281B2 JP H0464281 B2 JPH0464281 B2 JP H0464281B2 JP 60243953 A JP60243953 A JP 60243953A JP 24395385 A JP24395385 A JP 24395385A JP H0464281 B2 JPH0464281 B2 JP H0464281B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- slip
- surface layer
- water
- 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.)
- Expired - Lifetime
Links
- 239000002344 surface layer Substances 0.000 claims description 27
- 239000011230 binding agent Substances 0.000 claims description 15
- 239000010410 layer Substances 0.000 claims description 12
- 239000003232 water-soluble binding agent Substances 0.000 claims description 12
- 238000007569 slipcasting Methods 0.000 claims description 10
- 238000000465 moulding Methods 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 238000007711 solidification Methods 0.000 claims 1
- 230000008023 solidification Effects 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000000919 ceramic Substances 0.000 description 9
- 239000002131 composite material Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 230000003014 reinforcing effect Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 239000011505 plaster Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229910052845 zircon Inorganic materials 0.000 description 2
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Landscapes
- Producing Shaped Articles From Materials (AREA)
Description
【発明の詳細な説明】
〔発明の利用分野〕
本願発明は例えばセラミツク粒、金属粒、炭素
粒などの耐火性粒子のスリツプ(泥しよう)を鋳
込んで成形品を造るスリツプキヤステイング用鋳
型に係り、特に複雑形状の成形品を造るに好適な
鋳型に関する。[Detailed Description of the Invention] [Field of Application of the Invention] The present invention is applicable to slip casting molds for making molded products by casting slips of refractory particles such as ceramic particles, metal particles, carbon particles, etc. In particular, the present invention relates to a mold suitable for making molded products with complex shapes.
スリツプキヤステイング法で得られるグリーン
ボデイは強度が弱いので、鋳型からの離型が難し
い。特に形状が複雑なグリーンボデイを得ること
や内部に空間を有する形状品の成形は鋳型の分
割、鋳型の除去方法等の制約がある。
The green body obtained by the slip casting method has low strength, so it is difficult to release it from the mold. In particular, when it comes to obtaining a green body with a complex shape or molding a shaped product with an internal space, there are restrictions such as mold division and mold removal methods.
スリツプ鋳込み後の鋳型を除去する方法には例
えば特公昭58−125658号公報に開示されるように
鋳型を組込んだまま焼結し、崩壊除去する方法が
あるが、鋳型に組込んだまま大気中放置、乾燥す
るため、また、鋳型を組込んだまま焼結するた
め、形状が複雑なものでは乾燥時、および焼結時
に生じる鋳型および成形品の収縮、変形により、
成形品に割れが生じる。また、この引例は中子鋳
型の使用を想定したものではない。 There is a method for removing the mold after slip casting, for example, as disclosed in Japanese Patent Publication No. 58-125658, in which the mold is sintered with the mold in place and then disintegrated and removed. Because the product is left to dry and is sintered with the mold still in place, if the shape is complex, shrinkage and deformation of the mold and molded product may occur during drying and sintering.
Cracks occur in the molded product. Furthermore, this reference does not assume the use of core molds.
一方、特開昭57−176107号公報に開示されるよ
うに温水崩壊性石膏鋳型にスリツプを流し込み、
固化させた成形品と鋳型を約85℃以上の温水に浸
漬して、石膏鋳型を除去する方法もあるが、浸漬
中に成形品が崩壊しないよう結合剤を添加してお
り、これが成形品の機械的性質に影響を与え、ま
た奥部まで温水で崩壊させるには長時間を要す
る。 On the other hand, as disclosed in Japanese Patent Application Laid-Open No. 57-176107, a slip is poured into a hot water disintegrating plaster mold,
There is also a method of removing the plaster mold by immersing the solidified molded product and casting mold in warm water of approximately 85°C or higher, but a binder is added to prevent the molded product from collapsing during soaking, and this prevents the molding from collapsing. It affects the mechanical properties and requires a long time to disintegrate deep inside with hot water.
本願発明は上記に鑑み、形状が複雑な成形体を
スリツプキヤステイングで成形するに際し、鋳型
の除去が容易となるような最適鋳型構成及びその
造型に用いる粘結剤を提供することを目的とす
る。
In view of the above, an object of the present invention is to provide an optimal mold configuration that facilitates removal of the mold when molding a molded object with a complex shape by slip casting, and a binder used for molding the mold. .
本願発明は、鋳型空洞面側にスリツプ中の溶媒
の吸収により強度が低下する鋳型材で形成する第
1表面層を設け、その外側に第1表面層より高強
度の第2層を設け、第1表面層をスリツプ中に含
まれる溶媒に応じて、有機溶剤に可溶な粘結剤又
は水溶性粘結剤を用いて造型することにより達成
される。
The present invention provides a first surface layer formed of a mold material whose strength decreases due to absorption of solvent in the slip on the mold cavity side, and a second layer having higher strength than the first surface layer outside of the first surface layer. This is achieved by molding one surface layer using a binder soluble in an organic solvent or a binder soluble in water, depending on the solvent contained in the slip.
スリツプキヤステイングにおいて、鋳型からグ
リーンボデイを傷つけることなく容易に除去する
ためには、スリツプが固化し、グリーンボデイが
生成した時、グリーンボデイ周辺の鋳型強度が低
下していることが必要である。 In slip casting, in order to easily remove the green body from the mold without damaging it, when the slip hardens and the green body is generated, it is necessary that the strength of the mold around the green body is reduced.
即ち、(i)スリツプの固化と共に強度が低下する
鋳型、(ii)強度の弱い鋳型等を使用すれば良い。 That is, (i) a mold whose strength decreases as the slip solidifies, and (ii) a mold whose strength is weak may be used.
一方、実際のスリツプキヤステイングでは2つ
以上の鋳型を組合せることを考えると鋳型全体に
おいて、強度が低下する〔(i)〕或いは強度の小さ
な鋳型〔(ii)〕はグリーンボデイ近傍のみで良いか
ら、鋳型空洞部の第1表面層以外は強度が高い方
が望ましい。 On the other hand, in actual slip casting, when two or more molds are combined, the strength of the entire mold is reduced [(i)], or the mold with low strength [(ii)] is sufficient only in the vicinity of the green body. Therefore, it is desirable that the layers other than the first surface layer of the mold cavity have high strength.
即ち、第1図に示すように鋳型空洞面側第1表
面層1とその外側にそれより強度が高い第2層2
を複合させた鋳型がスリツプキヤステイング用鋳
型として有効である。このような複合化した鋳型
を組合せ、鋳型空洞部にスリツプを流込み、スリ
ツプを固化(グリーンボデイ4生成)せしめた
後、離型すれば、グリーンボデイ表面近傍は強度
が低下しているので、鋳型の方が崩壊し、グリー
ンボデイが壊れることはない。 That is, as shown in FIG. 1, there is a first surface layer 1 on the side of the mold cavity, and a second layer 2 having higher strength on the outside thereof.
A composite mold is effective as a slip casting mold. When such composite molds are combined, the slip is poured into the mold cavity, the slip is solidified (green body 4 is generated), and the mold is released, the strength near the surface of the green body has decreased. The mold will collapse and the green body will not.
鋳型第2層2は第1表面層1を補強する目的で
あり、石膏型、セラミツク型、耐熱性樹脂型を用
いることができ、これらは繰返し使用することが
できる。 The purpose of the second mold layer 2 is to reinforce the first surface layer 1, and a plaster mold, a ceramic mold, or a heat-resistant resin mold can be used, and these molds can be used repeatedly.
従つて鋳型第1表面層が、スリツプの固化と共
に強度が低下する鋳型が有効であり、スリツプの
溶媒に溶解する粘結剤で鋳型した鋳型を用いるこ
とにより、この目的が達成されることを見いだし
た。 Therefore, it has been found that a mold in which the strength of the first surface layer of the mold decreases as the slip hardens is effective, and that this objective can be achieved by using a mold formed with a binder that dissolves in the solvent of the slip. Ta.
水を溶媒とするスリツプの場合は水溶性粘結剤
で作製した鋳型を用いれば良く、水溶性粘結剤と
しては有機質、無機質のものがある。 In the case of a slip using water as a solvent, a mold made of a water-soluble binder may be used, and water-soluble binders include organic and inorganic ones.
無機水溶性粘結剤となり得るものには炭酸塩類
(炭酸ナトリウム、炭酸カリウム)、硫酸塩類(硫
酸アンモニウム、硫酸水素ナトリウム、硫酸水素
カリウム、硫酸マグネシウム)、リン酸塩類(燐
酸3ナトリウム、燐酸3カリウム)、塩化物類
(塩化カリウム、塩化マグネシウム)がある。 Possible inorganic water-soluble binders include carbonates (sodium carbonate, potassium carbonate), sulfates (ammonium sulfate, sodium hydrogen sulfate, potassium hydrogen sulfate, magnesium sulfate), and phosphates (trisodium phosphate, tripotassium phosphate). , chlorides (potassium chloride, magnesium chloride).
また有機水溶性粘結剤となり得るものにはポリ
ビニールアルコール、メチルセルロース、カルボ
キシメチルセルロース、エチルセルロースなどが
ある。 Examples of organic water-soluble binders include polyvinyl alcohol, methyl cellulose, carboxymethyl cellulose, and ethyl cellulose.
これらの無機及び有機水溶性物質を水に溶解せ
しめて粘結剤として、鋳型骨材に混合したものを
鋳型材として用いる。 These inorganic and organic water-soluble substances are dissolved in water and used as a binder, and mixed with mold aggregate to be used as a mold material.
鋳型骨材としてはアルミナ、マグネシア、ジル
コンサンド、珪砂の他、非耐火粒子も使用でき
る。 In addition to alumina, magnesia, zircon sand, and silica sand, non-refractory particles can also be used as the mold aggregate.
無機質及び有機質の水溶性粘結剤を用いた場合
の鋳型骨材の結合、スリツプ中の溶媒(水)を吸
収して、スリツプを固化せしめると同時に鋳型自
身の強度が低下する機構は次の通りである。 The mechanism by which the mold aggregate binds when using inorganic and organic water-soluble binders, absorbs the solvent (water) in the slip, solidifies the slip, and at the same time reduces the strength of the mold itself is as follows. It is.
第2図a,b,cに示すように、鋳型骨材中の
粒子5は未乾燥の状態では水溶性粘結剤6で被覆
されているが、(a参照)乾燥され硬化した鋳型
では水分は蒸発して内部に微細な空孔7が形成さ
れ、このような鋳型にスリツプを鋳込むとスリツ
プ中の水分(その他溶液も含む)は空孔7内に浸
入して水溶性粘結剤6の粘結力を弱め、各粒子5
を独立させる(c参照)。この結果、強度の低い
除去容易な鋳型が生成し、他方スリツプは水分を
放出してグリーンボデイが生成する。 As shown in Figures 2a, b, and c, particles 5 in the mold aggregate are coated with water-soluble binder 6 in the wet state, but (see a) the particles 5 in the mold aggregate are coated with water-soluble binder 6 in the dried and hardened mold. evaporates to form fine pores 7 inside, and when a slip is cast into such a mold, the moisture in the slip (including other solutions) enters into the pores 7 and forms the water-soluble binder 6. Weakening the cohesive force of each particle 5
(see c). This results in a mold that is less strong and easier to remove, while the slip releases moisture and produces a green body.
鋳型はスリツプ中の水分を吸収するに従いスリ
ツプの接触界面より崩壊可能な鋳型に移行する
が、他方スリツプは水分を放出するに従い収縮、
変形量を増加し、グリーンボデイの生成に至る。
しかるに本願発明においては、水分の吸収に伴つ
て、鋳型表面(スリツプとの界面)は軟化するの
でグリーンボデイの生成過程で発生する収縮、変
形を鋳型は阻害しない。このために割れの発生が
認められないグリーンボデイを得ることができ
る。 As the mold absorbs moisture in the slip, it becomes a collapsible mold from the contact interface of the slip, but on the other hand, as the slip releases moisture, it shrinks.
The amount of deformation is increased, leading to the generation of a green body.
However, in the present invention, as the mold surface (interface with the slip) softens as moisture is absorbed, the mold does not inhibit shrinkage and deformation that occur during the green body production process. Therefore, a green body without any cracks can be obtained.
また鋳型は吸水により強度が低下しているので
鋳型の除去が極めて容易になる。 Furthermore, since the strength of the mold is reduced due to water absorption, it becomes extremely easy to remove the mold.
また、セラミツクの材質により、水以外の溶剤
例えば有機溶剤をスリツプの媒液に用いることが
ある。この場合は前記機構にのつとり第1表面層
の鋳型骨材の粘結剤として媒液に用いられる有機
溶剤に可溶な粘結剤を用いれば良い。例えばスリ
ツプの媒液がアセトンあるいはエチルアルコール
の場合には骨材の粘結剤としてはアクリロニトリ
ル、スチレンポリマー、ポリ酢酸ビニル、酢酸セ
ルロース系樹脂、ポリ塩化ビニル樹脂などがあ
る。 Further, depending on the material of the ceramic, a solvent other than water, such as an organic solvent, may be used as the slip medium. In this case, a binder soluble in the organic solvent used as the medium may be used as the binder for the mold aggregate of the first surface layer according to the above-mentioned mechanism. For example, when the slip medium is acetone or ethyl alcohol, the binder for the aggregate may include acrylonitrile, styrene polymer, polyvinyl acetate, cellulose acetate resin, polyvinyl chloride resin, etc.
〔実施例 1〕
第3図に示したケーシング8を第1図に示した
本願発明の複合鋳型を用いてスリツプキヤステイ
ングで成形する例について説明する。
[Example 1] An example in which the casing 8 shown in FIG. 3 is molded by slip casting using the composite mold of the present invention shown in FIG. 1 will be described.
第1図の補強のための鋳型第2層2は、ジルコ
ンと溶融石英にアルミナゾルを加え混合して成形
焼成したものを用いた。この第2層2に別の模型
を設置し、空間部に炭酸カリウム水溶液を粘結剤
とする鋳型材を入れ、つき固めた後、模型を脱型
し、第1表面層1を硬化させるため、200℃で2
時間乾燥した。なお、第1表面層の配合比は水
100c.c.に対して炭酸カリウム80gを溶解させた水
溶液をアルミナ(250メツシユ以下)100gに25c.c.
添加、混合したものである。 The second layer 2 of the reinforcing mold shown in FIG. 1 was made by adding and mixing alumina sol to zircon and fused quartz, and molding and firing the mixture. Another model is installed in this second layer 2, a molding material containing potassium carbonate aqueous solution as a binder is put in the space, and after compacting, the model is demolded and the first surface layer 1 is hardened. , 2 at 200℃
Dry for an hour. The blending ratio of the first surface layer is water.
Add an aqueous solution of 80g of potassium carbonate to 100c.c. to 100g of alumina (250 mesh or less) to 25c.c.
It is added and mixed.
これらの複合型に第1表面層と同一組成で作製
した中子3を配設し、窒化ケイ素スリツプ(窒化
ケイ素100gに対して水32c.c.を加えたもの)を流
し込んだ。2時間後、各部分が固化したことを確
認し、上下補強型第2層2を離型したところ、固
化したセラミツク2のグリーンボデイ4の周囲に
少量の水溶性鋳型(鋳型第1表面層)を残し、離
型ができた。その後、ハケの柔らかな筆で残存し
た第1表面層の残部をとり除き、第3図に示した
セラミツク製ケーシングが得られた。 A core 3 made of the same composition as the first surface layer was placed in these composite molds, and silicon nitride slip (32 c.c. of water was added to 100 g of silicon nitride) was poured into the mold. After 2 hours, it was confirmed that each part had solidified, and the upper and lower reinforcing mold second layer 2 was released from the mold, and a small amount of water-soluble mold (mold first surface layer) was formed around the green body 4 of the solidified ceramic 2. The mold was released by leaving behind. Thereafter, the remaining portion of the first surface layer was removed with a soft brush to obtain the ceramic casing shown in FIG. 3.
〔実施例 2〕
補強のための鋳型第2層2は石膏型とし、鋳型
第1表面層をポリビニールアルコールを粘結剤と
する鋳型材で実施例1と同じ方法で複合型を作製
した。[Example 2] A composite mold was produced in the same manner as in Example 1 using a plaster mold as the second layer 2 of the reinforcing mold and a mold material containing polyvinyl alcohol as a binder for the first surface layer of the mold.
なお、鋳型第1表面層の配合比は、水100c.c.に
ポリビニールアルコール25gを溶解させた水溶液
をアルミナ(250メツシユ、85重量部、125メツシ
ユ、15重量部)に32c.c.添加、混合したものであ
り、第1表面層の乾燥のため、複合化した鋳型を
60℃で24時間保持した。 The blending ratio of the first surface layer of the mold is to add 32 c.c. of an aqueous solution of 25 g of polyvinyl alcohol dissolved in 100 c.c. of water to alumina (250 mesh, 85 parts by weight, 125 mesh, 15 parts by weight). , and in order to dry the first surface layer, the composite mold is
It was kept at 60°C for 24 hours.
この鋳型にアルミナスリツプ(アルミナ100g
に対して水35c.c.を添加したもの)流し込んだとこ
ろ実施例1と同様、簡単に、しかもグリーンボデ
イに割れを発生することなく第3図に示すセラミ
ツク製ケーシングが得られた。 Add alumina strip (100g of alumina) to this mold.
35 c.c. of water was added), and as in Example 1, the ceramic casing shown in FIG. 3 was obtained easily and without any cracks in the green body.
以上説明したように、本願発明によれば鋳型第
1表面層とこれを補強する第2層からなる複合鋳
型の第1表面層を造型するに際し、スリツプ中に
含まれる溶媒に応じて有機溶剤に可溶な粘結剤又
は水溶性粘結剤を用いることにより、鋳型第1表
面層はスリツプの溶剤を吸収して鋳型除去が極め
て容易な程度に軟化するため、離型中にグリーン
ボデイ表面の拘速が弱くなり、簡単に離型でき複
雑形状品の成形が可能となる。
As explained above, according to the present invention, when molding the first surface layer of a composite mold consisting of the first surface layer of the mold and the second layer reinforcing it, an organic solvent is used depending on the solvent contained in the slip. By using a soluble binder or a water-soluble binder, the first surface layer of the mold absorbs the slip solvent and softens to the extent that removal of the mold is extremely easy. The confinement speed becomes weaker, allowing for easier mold release and the molding of complex-shaped products.
更に、グリーンボデイの収縮変形は軟化した鋳
型第1表面層で吸収するようになるため、グリー
ンボデイの生成過程での割れ防止が画られる。 Furthermore, shrinkage deformation of the green body is absorbed by the softened first surface layer of the mold, thereby preventing cracking during the production process of the green body.
第1図は本願発明を説明するためのセラミツク
製ケーシングの成形用鋳型の縦断面図、第2図は
本願発明の第1表面層の乾燥、及び水を吸収した
崩壊する原理の説明図、第3図は本願発明の実施
例のために成形したセラミツク製ケーシングの外
観図である。
1…鋳型第1表面層、2…鋳型第2層(補強
層)、3…中子、4…セラミツクグリーンボデイ、
5…鋳型の骨材、6…水溶性粘結剤、7…空孔。
FIG. 1 is a longitudinal cross-sectional view of a mold for forming a ceramic casing to explain the present invention, FIG. FIG. 3 is an external view of a ceramic casing molded for an embodiment of the present invention. 1... Mold first surface layer, 2... Mold second layer (reinforcing layer), 3... Core, 4... Ceramic green body,
5... Aggregate of mold, 6... Water-soluble binder, 7... Holes.
Claims (1)
後に鋳型を除去する成形法に用い、スリツプに接
する鋳型空洞面側第1表面層と、第1表面層の外
側に第1表面層より強度が高い第2層とを複合さ
せたスリツプキヤステイング用鋳型において、前
記鋳型空洞面側の第1表面層は粘結剤と鋳型骨材
からなるとともにスリツプ中の溶媒の吸収により
軟化するものであつて、前記粘結剤は無機質の水
溶性粘結剤、有機質の水溶性粘結剤及び有機溶剤
に可溶な粘結剤の群から選ばれるものであること
を特徴とするスリツプキヤステイング用鋳型。1 Used in a molding method in which a slip is cast into a mold and the mold is removed after solidification of the slip, a first surface layer on the side of the mold cavity that is in contact with the slip, and a second surface layer having higher strength than the first surface layer on the outside of the first surface layer. In a slip casting mold comprising two layers, the first surface layer on the side of the mold cavity is made of a binder and a mold aggregate, and is softened by absorption of solvent in the slip; A slip casting mold, characterized in that the binder is selected from the group of inorganic water-soluble binders, organic water-soluble binders, and binders soluble in organic solvents.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24395385A JPS62104704A (en) | 1985-11-01 | 1985-11-01 | Slip casting molding mold |
US06/883,759 US4883621A (en) | 1985-07-12 | 1986-07-09 | Method for forming cast article by slip casting |
DE8686305366T DE3681362D1 (en) | 1985-07-12 | 1986-07-11 | METHOD FOR PRODUCING SHAPES BY SLICK ENERGY. |
EP86305366A EP0210027B1 (en) | 1985-07-12 | 1986-07-11 | Method for forming cast article by slip casting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24395385A JPS62104704A (en) | 1985-11-01 | 1985-11-01 | Slip casting molding mold |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62104704A JPS62104704A (en) | 1987-05-15 |
JPH0464281B2 true JPH0464281B2 (en) | 1992-10-14 |
Family
ID=17111492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24395385A Granted JPS62104704A (en) | 1985-07-12 | 1985-11-01 | Slip casting molding mold |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62104704A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54129011A (en) * | 1978-03-14 | 1979-10-06 | Inst Skkla I Ceramiki | Mold for forming ceramic products |
JPS59190811A (en) * | 1983-04-15 | 1984-10-29 | 株式会社日立製作所 | Mold for slip casting |
-
1985
- 1985-11-01 JP JP24395385A patent/JPS62104704A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54129011A (en) * | 1978-03-14 | 1979-10-06 | Inst Skkla I Ceramiki | Mold for forming ceramic products |
JPS59190811A (en) * | 1983-04-15 | 1984-10-29 | 株式会社日立製作所 | Mold for slip casting |
Also Published As
Publication number | Publication date |
---|---|
JPS62104704A (en) | 1987-05-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR890003502B1 (en) | Method for shaping slip-casting and shaping moulds | |
US4812278A (en) | Process for preparing mold | |
US4808360A (en) | Method of producing mold for slip casting and method of molding slip casting | |
US4919193A (en) | Mold core for investment casting, process for preparing the same and process for preparing mold for investment casting having therewithin said mold core | |
KR890004247B1 (en) | Slip casting forming method and mold | |
JP2005537935A (en) | Sleeve, method for producing the same, and mixture for producing the same | |
JPH01262041A (en) | Manufacture of mold and core | |
JPH0464281B2 (en) | ||
JP2006175510A (en) | Method and device for molding water-soluble core | |
JPH037486B2 (en) | ||
JPH0636954B2 (en) | Composition for easily disintegrating mold | |
JP2641444B2 (en) | Core for pressure casting and manufacturing method thereof | |
JPH039841B2 (en) | ||
JPH0150561B2 (en) | ||
JPH036881B2 (en) | ||
JPS61239904A (en) | Slip casting molding method and mold for molding | |
JPS60253505A (en) | Manufacture of ceramics product | |
JPS6358082B2 (en) | ||
JPH043884B2 (en) | ||
JPH0339774B2 (en) | ||
JPH11320075A (en) | Molding for cylinder block and its production | |
JPS6330202A (en) | Manufacture of ceramics baked body | |
JPS642481B2 (en) | ||
JPS6223705A (en) | Mold for slip casting | |
JPH08117925A (en) | Heat insulating pad for casting, its production and material for producing the pad |