JPS61209960A - Manufacture of electrocasted refractories - Google Patents
Manufacture of electrocasted refractoriesInfo
- Publication number
- JPS61209960A JPS61209960A JP60050366A JP5036685A JPS61209960A JP S61209960 A JPS61209960 A JP S61209960A JP 60050366 A JP60050366 A JP 60050366A JP 5036685 A JP5036685 A JP 5036685A JP S61209960 A JPS61209960 A JP S61209960A
- Authority
- JP
- Japan
- Prior art keywords
- casting
- refractories
- mold
- glass
- thermoplastic film
- 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
Landscapes
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
1、の
この発明はアルミナ、ジルコニア、シリカ質電鋳耐火物
の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention (1) relates to a method for producing alumina, zirconia, and siliceous electroformed refractories.
【Lへ11
アルミナ、ジルコニア、シリカ質電鋳耐火物はAZS耐
火物と称されガラス工業用耐火物として広く用いられて
いる。AZS耐火物は、電気孤光炉により所定の配合原
料を溶融し、主として珪砂を結合した鋳型に鋳造したあ
と、徐冷して製造されている。この鋳型を形成する際、
珪砂を結合する目的で水ガラスを結合剤として用いる場
合もあるが、珪砂の製品への焼付き、鋳型強度の不足又
は空気中の水分の吸収による強度の低下、吸収した水分
が鋳造物に侵入して気孔を発生するなどの欠点がある。[To L11 Alumina, zirconia, and siliceous electrocast refractories are called AZS refractories and are widely used as refractories for the glass industry. AZS refractories are manufactured by melting a predetermined blended raw material in an electric arc furnace, casting the melt into a mold mainly bonded with silica sand, and then slowly cooling the melt. When forming this mold,
Water glass is sometimes used as a binder to bind silica sand, but silica sand may seize on the product, strength may decrease due to lack of mold strength or absorption of moisture from the air, and absorbed moisture may enter the casting. There are disadvantages such as the generation of pores.
また、水ガラスを結合剤とした場合、使用済の珪砂は、
鋳造時の溶湯の温度が1900℃にも達するので、かな
り長時間高温にさらされるため、焼結して再生使用が困
難である。In addition, when water glass is used as a binder, used silica sand
Since the temperature of the molten metal during casting reaches as high as 1900°C, it is exposed to high temperatures for quite a long time, making it difficult to sinter and reuse.
また、再粉砕しても、水ガラス由来のアルカリ残留のた
め、耐火度が低下し単独では再使用に耐えないという欠
点も存在する。Furthermore, even if re-pulverized, the alkali derived from water glass remains, resulting in a decrease in fire resistance and the drawback that it cannot be reused alone.
一方、フェノール、フランなどの有機質結合剤は結合強
度が大きく強度の経時劣化が起り難いが、有機質結合剤
から鋳込物製品表面への浸炭現象や、結合剤から発生す
るガスの鋳造物への侵入や、その結果生じる気孔の発生
など、製品の品質面への悪影響がある。特に近年は高品
質ガラス、例えばテレビ用ブラウン管やフォトマスクの
如きエレクトロニクス用ガラスを製造する場合、ガラス
溶解炉用耐火物の品質が極めて重要であり、耐火物とガ
ラスの反応界面でガラス中に気泡を発生する耐火物は使
用に耐えない。溶融ガラス内での気泡の発生の原因につ
いては多くの理論や経験上の法則が知られている。これ
らの理論から、ガラス溶解炉用耐火物には、次のような
ことが必要であるとされている。On the other hand, organic binders such as phenol and furan have high bond strength and are unlikely to deteriorate over time, but they may cause carburization from the organic binder to the surface of the cast product or gas generated from the binder to the cast product. There are negative effects on product quality, such as intrusion and the resulting formation of pores. Particularly in recent years, when manufacturing high-quality glass, such as glass for electronics such as cathode ray tubes for televisions and photomasks, the quality of refractories for glass melting furnaces is extremely important. Refractories that generate this cannot withstand use. Many theories and empirical rules are known about the causes of bubble formation in molten glass. Based on these theories, it is said that the following requirements are required for refractories for glass melting furnaces.
(1)耐火物が気孔のない緻密な組織であること。(1) The refractory has a dense structure without pores.
(2)鉄、その他の金属を含まず、また、その酸化物も
極めて少ないこと。(2) Contains no iron or other metals, and contains very little oxide thereof.
(3)耐火物の組成が高い酸化度を維持すること。(3) The refractory composition maintains a high degree of oxidation.
しかしながら、酸化度については測定方法が明らかでな
く、現実的には、なるべく高い酸化状態を溶解、鋳造、
徐冷の各過程で維持することが唯一のものとなっている
。However, the method for measuring the degree of oxidation is not clear, and in reality, the highest possible oxidation state is melted, cast, or
It is the only thing that must be maintained during each step of slow cooling.
有機結合剤を使用する場合に、それに起因する製品の品
質への悪影響を予防することを目的として本出願人は特
願昭57−61105号発明を提案し、鋳型配合物中に
予め酸化剤を配して炭素及び還元性ガスの酸化を行わせ
鋳造物への悪影響を排除することに成功した。In order to prevent the adverse effects on product quality caused by organic binders when using organic binders, the present applicant proposed the invention of Japanese Patent Application No. 57-61105, in which an oxidizing agent is added to the mold mixture in advance. We succeeded in eliminating the negative effects on the castings by oxidizing carbon and reducing gases.
が °しようとする 、
しかしながら、酸化剤は高価であり、また化学物質の取
扱いに注意を要するし、NOxの排出などの問題が存在
する。However, oxidizing agents are expensive, chemicals must be handled with care, and there are problems such as NOx emissions.
1111江
本発明は従来のアルミナ、ジルコニア、シリカ質電鋳耐
火物の製造方法を改良して、より勝れた品質のAZS耐
火物をガラス工業界へ供給することのできる電鋳耐火物
の製造方法を提供することを目的としている。The present invention improves the conventional manufacturing method of alumina, zirconia, and siliceous electrocast refractories, and provides a method for manufacturing electrocast refractories that can supply AZS refractories of superior quality to the glass industry. is intended to provide.
口 、を ゛するための
アルミナ、ジルコニア、シリカ質の電鋳耐火物を製造す
る方法において、結合剤を用いることなく熱可塑性フィ
ルムを介して型砂内を負圧に保持して鋳型を形成し、鋳
造後も負−圧を維持し、外気である空気又は酸化性気体
を鋳造物に接触させて鋳造物を酸化状態に維持すること
を特徴とする電鋳耐火物の製造方法。In a method for producing electroformed refractories made of alumina, zirconia, and silica for use in refractories, a mold is formed by maintaining negative pressure in mold sand via a thermoplastic film without using a binder, A method for producing electrocast refractories, which comprises maintaining a negative pressure even after casting and bringing outside air or an oxidizing gas into contact with the casting to maintain the casting in an oxidized state.
作n呈−
前述のごと(結合剤を用いない造型法をとつているため
、前述の有機又は無機の結合剤を用いる場合に生ずる幾
多の問題を一挙に解消することができる。さらに、溶渇
の鋳造により熱可塑性フィルムが溶融、消失したあと、
外気等を接触させるため、鋳造物の表面を十分な酸化状
態に所望の時間保持し得る。また更に必要であれば鋳造
枠の全体を酸素など酸化性の雰囲気の適当な大きさの密
室に挿入して、その中に吸引する外気を高い酸化性ガス
にすることができる。Production - As mentioned above (because the molding method does not use a binder, it is possible to solve all the problems that occur when using organic or inorganic binders as described above at once. After the thermoplastic film melts and disappears by casting,
By contacting with outside air or the like, the surface of the casting can be maintained in a sufficiently oxidized state for a desired period of time. Furthermore, if necessary, the entire casting frame can be inserted into a suitably sized closed chamber containing an oxidizing atmosphere such as oxygen, and the outside air drawn into the chamber can be made into a highly oxidizing gas.
本発明の方法によって得たAZS耐火物は外観上明黄色
であり、対ガラス発泡性は極めて小さい。特に従来しば
しば起きていた鋳造面に近い高発泡性部分の存在(これ
は鋳型結合剤に起因した浸炭又は部分的還元に起因する
と考えられている)が見られない。The AZS refractory obtained by the method of the present invention has a bright yellow appearance and has extremely low foamability against glass. In particular, the presence of a highly foamable area close to the casting surface (which is believed to be due to carburization or partial reduction caused by the mold binder), which has often occurred in the past, is not observed.
支i乱 次に図面を参照して実施例について説明する。support Next, embodiments will be described with reference to the drawings.
先ず第1図(イ)に示すような所定寸法の木製の模型5
を製作する。First, a wooden model 5 with predetermined dimensions as shown in FIG.
Manufacture.
第1図(イ)において、排気ロアと通気孔14を持った
台6を用意する。排気ロアと通気孔14は台6の中で通
じている。この台6の上に穴4をあけた木製の模型5を
乗せる。In FIG. 1(A), a stand 6 having an exhaust lower and a ventilation hole 14 is prepared. The exhaust lower and the ventilation hole 14 communicate within the platform 6. A wooden model 5 with a hole 4 drilled therein is placed on this stand 6.
穴4は通気孔14の位置と重なるようにしておく。この
木製の模型5の上にスブリューの模型3を乗せる。木製
の模型5の上方には熱可塑性フィルム2とこれを加熱す
るヒーター1を用意する。The hole 4 is made to overlap the position of the ventilation hole 14. Place Soubreu model 3 on top of this wooden model 5. A thermoplastic film 2 and a heater 1 for heating the film are provided above the wooden model 5.
次に第1図(ロ)において、排気ロアを真空ポンプ(図
示せず)につなぎ、排気しながらヒーター1で熱可塑性
フィルム2を加熱して柔らかくして木製の模型5の上に
被せる。Next, in FIG. 1(b), the exhaust lower is connected to a vacuum pump (not shown), and while the exhaust is being exhausted, the thermoplastic film 2 is heated by the heater 1 to soften it and placed on the wooden model 5.
柔らかい熱可塑性フィルム2は穴4から真空に吸引され
ているので、木製の模型5にびつたりと密着する。Since the soft thermoplastic film 2 is vacuumed through the holes 4, it tightly adheres to the wooden model 5.
第1図(ハ)において、台6の上に鋳造枠15を乗せて
木製の模型5の周りにケイ砂8を密に充1.1−する。In FIG. 1(c), a casting frame 15 is placed on a stand 6, and silica sand 8 is densely filled around the wooden model 5 (1.1-).
排気口10から排気しながら、柔らかくしだ熱可塑性フ
ィルム9をケイ砂8の上に被せる。この結果、熱可塑性
フィルム9はケイ砂8にぴったりと密着し、ケイ砂8の
内部は減圧の状態になり、流動性を全く失った状態とな
る。この状態で排気ロアからの排気を止め、台6を取り
去り、さらに木製の鋳型5とスブリューの模型3を取り
去る。While exhausting the air through the exhaust port 10, a soft, weeping thermoplastic film 9 is placed over the silica sand 8. As a result, the thermoplastic film 9 tightly adheres to the silica sand 8, and the interior of the silica sand 8 is under reduced pressure, losing all fluidity. In this state, the exhaust from the exhaust lower is stopped, the stand 6 is removed, and the wooden mold 5 and the Souvreux model 3 are also removed.
排気口10からの排気は続けられているからケイ砂8は
崩れないで内部に木製の模型5と同じ形状の空洞を持つ
鋳型17となる
第1図(ニ)において、前述の第1図(イ)−(ハ)の
段階とほぼ同じ工程で別の鋳型18を作り、第1図〈ホ
)に示すように、先に ・作った鋳型17をこの
上に重ねると、内部に熱可塑性フィルム2と熱可塑性フ
ィルム13で囲まれたキャビティー16が出来る。Since the exhaust from the exhaust port 10 continues, the silica sand 8 does not collapse and becomes the mold 17 which has a cavity in the same shape as the wooden model 5. In FIG. Another mold 18 is made in almost the same process as steps a) to (c), and as shown in Fig. 1 (e), when the previously made mold 17 is placed on top of this, a thermoplastic film is formed inside. A cavity 16 surrounded by 2 and a thermoplastic film 13 is formed.
なお、第1図(イ)の符号19はフィルム保持具を示し
、第1図(ニ)の符号20は鋳造枠20、符号12は排
気口である。Note that the reference numeral 19 in FIG. 1(A) indicates a film holder, the reference numeral 20 in FIG. 1(D) indicates a casting frame 20, and the reference numeral 12 indicates an exhaust port.
1つの実験例を説明すれば、たとえば、厚さ100ミク
ロンの熱可塑性フィルム2.9.13を用い、珪砂8と
してはオーストラリア産フリーマントル珪砂を用いて寸
法i oox300x450msのキャビティー16を
形成し鋳型とした。排気状態を続けたまま、このキャビ
ティー16内にAZS溶瀉(商品名モノフラックスO8
−3)を注入路21から注入して鋳造した。鋳造後も3
0分間排気ポンプの駆動を続けて排気口10,12から
吸引し続けた。その後吸引を停止したあと鋳造物を砂に
埋没させてしまい3日間放冷した。冷却後、鋳造物を砂
から取り出したところ、外表面は明黄色を呈し、型砂の
焼き付きはほとんどなく、亀裂の発生も見られなかった
。また酸化の程度を表す対ガラス発泡性も低位であった
。また使用済の珪砂もなんらの雑物を含まず、繰り返し
再使用に耐えた。To explain one experimental example, for example, using a thermoplastic film 2.9.13 with a thickness of 100 microns and using Australian Fremantle silica sand as the silica sand 8, a cavity 16 with dimensions i oox 300 x 450 ms was formed, and a mold was formed. And so. While continuing the exhaust state, fill the cavity 16 with AZS melt (trade name: Monoflux O8).
-3) was injected from the injection path 21 and cast. 3 after casting
The exhaust pump continued to be driven for 0 minutes, and suction was continued from the exhaust ports 10 and 12. Thereafter, the suction was stopped, and the cast product was buried in sand and left to cool for 3 days. When the casting was taken out from the sand after cooling, the outer surface was bright yellow, there was almost no burning of the molding sand, and no cracks were observed. Furthermore, the foamability against glass, which indicates the degree of oxidation, was also low. Furthermore, the used silica sand did not contain any impurities and could withstand repeated reuse.
表1は対ガラス発泡性の比較実験の結果を示す。Table 1 shows the results of comparative experiments on foaming properties against glass.
である。
1・・・・・・・・・ヒーター
2.9.13・・・・熱可塑性フィルム3.5・・・・
・・・模型
6・・・・・・・・・台
8・・・・・・・・・ケイ砂
16・・・・・・・・キャビティ−
表−二り
使用ガラス:ソーダ石灰ガラス
製造温度: 1200℃
池数(個/Cm2)
表面部 内部
通常(7)AZS耐火物 120 150(特願昭5
7−61105号の方法による)本発明による
AZS耐火物 87
発泡性が極めて
低いアルミナ質
電鋳耐火物 O〜1 0〜1(商品名モノフ
ラックスM)
〈注〉
耐火物試料(直径40mm長さ7mm)を1200℃で
1時間仮焼したあと、そのままその上にガラス試料(直
径20mm長さ5mm)をのせ、1時間保持し、その後
炉外で放冷した。池数は顕微鏡を用いて計数し、単位面
積当りの池数を計算した。
!Q ψIt is. 1... Heater 2.9.13... Thermoplastic film 3.5...
・・・Model 6・・・・・・・・・Table 8・・・・・・ Silica sand 16・・・・・・Cavity - Table - 2 Glass used: Soda lime glass manufacturing temperature : 1200℃ Number of ponds (pieces/cm2) Surface part Internal normal (7) AZS refractory 120 150 (Patent application 1973)
AZS refractory according to the present invention (according to the method of No. 7-61105) 87 Alumina electrocast refractory with extremely low foamability O~1 0~1 (trade name Monoflux M) Note: Refractory sample (diameter 40 mm length) 7 mm) was calcined at 1200° C. for 1 hour, a glass sample (diameter 20 mm, length 5 mm) was placed on top of the sample, held for 1 hour, and then allowed to cool outside the furnace. The number of ponds was counted using a microscope, and the number of ponds per unit area was calculated. ! Q ψ
Claims (1)
製造する方法において、結合剤を用いることなく熱可塑
性フィルムを介して型砂内を負圧に保持して鋳型を形成
し、鋳造後も負圧を維持し、外気である空気又は酸化性
気体を鋳造物に接触させて鋳造物を酸化状態に維持する
ことを特徴とする電鋳耐火物の製造方法。(1) In a method for manufacturing alumina, zirconia, and siliceous electroformed refractories, a mold is formed by maintaining negative pressure in mold sand through a thermoplastic film without using a binder, and the mold remains under negative pressure after casting. A method for manufacturing an electrocast refractory, which comprises maintaining the casting in an oxidized state by maintaining pressure and bringing outside air or an oxidizing gas into contact with the casting.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60050366A JPS61209960A (en) | 1985-03-15 | 1985-03-15 | Manufacture of electrocasted refractories |
FR858516742A FR2578835B1 (en) | 1985-03-15 | 1985-11-13 | PROCESS AND APPARATUS FOR MANUFACTURING CAST REFRACTORIES |
US07/120,174 US4943398A (en) | 1985-03-15 | 1987-11-12 | Method for manufacturing a fused cast refractory |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60050366A JPS61209960A (en) | 1985-03-15 | 1985-03-15 | Manufacture of electrocasted refractories |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61209960A true JPS61209960A (en) | 1986-09-18 |
JPH0520388B2 JPH0520388B2 (en) | 1993-03-19 |
Family
ID=12856889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60050366A Granted JPS61209960A (en) | 1985-03-15 | 1985-03-15 | Manufacture of electrocasted refractories |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61209960A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01215764A (en) * | 1987-12-28 | 1989-08-29 | Ppg Ind Inc | Treatment of melting injection type ceramic refractory |
CN108580805A (en) * | 2018-04-23 | 2018-09-28 | 芜湖市华邦流体科技有限公司 | A kind of vacuum casting for butterfly plate casting |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS508409A (en) * | 1973-05-21 | 1975-01-28 | ||
JPS50128707A (en) * | 1974-04-02 | 1975-10-11 | ||
JPS51119005A (en) * | 1975-04-11 | 1976-10-19 | Toshiba Monofrax | Refractory for highhtemperature melting tank |
-
1985
- 1985-03-15 JP JP60050366A patent/JPS61209960A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS508409A (en) * | 1973-05-21 | 1975-01-28 | ||
JPS50128707A (en) * | 1974-04-02 | 1975-10-11 | ||
JPS51119005A (en) * | 1975-04-11 | 1976-10-19 | Toshiba Monofrax | Refractory for highhtemperature melting tank |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01215764A (en) * | 1987-12-28 | 1989-08-29 | Ppg Ind Inc | Treatment of melting injection type ceramic refractory |
CN108580805A (en) * | 2018-04-23 | 2018-09-28 | 芜湖市华邦流体科技有限公司 | A kind of vacuum casting for butterfly plate casting |
Also Published As
Publication number | Publication date |
---|---|
JPH0520388B2 (en) | 1993-03-19 |
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