JPS5935068A - Basic castable - Google Patents

Basic castable

Info

Publication number
JPS5935068A
JPS5935068A JP57142898A JP14289882A JPS5935068A JP S5935068 A JPS5935068 A JP S5935068A JP 57142898 A JP57142898 A JP 57142898A JP 14289882 A JP14289882 A JP 14289882A JP S5935068 A JPS5935068 A JP S5935068A
Authority
JP
Japan
Prior art keywords
magnesia
metal powder
addition
basic
oxidation
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
Application number
JP57142898A
Other languages
Japanese (ja)
Inventor
古川 邦男
利幸 鈴木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Harima Refractories Co Ltd
Original Assignee
Harima Refractories Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Harima Refractories Co Ltd filed Critical Harima Refractories Co Ltd
Priority to JP57142898A priority Critical patent/JPS5935068A/en
Publication of JPS5935068A publication Critical patent/JPS5935068A/en
Pending legal-status Critical Current

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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】 本発明は、緻密で争又はスラグの浸透を防止するのにす
ぐれた効果を示す塩基性キャスタブルに係るものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a basic castable that is dense and exhibits excellent effectiveness in preventing the penetration of particles or slag.

近年、省エネルギーの観点から、耐火物は施工」二の融
通性に富む不定形耐火物の採用が著しく多くなって訃9
、殊に製鋼業における耐火物としては、塩基性スラグに
対する耐食性及び高耐火性等の点からみて塩基性材質、
特にマグネシア質のものが多く用いられでbる。
In recent years, from the perspective of energy conservation, the use of monolithic refractories, which are highly flexible in construction, has increased significantly.
In particular, as refractories in the steel manufacturing industry, basic materials,
In particular, magnesia-based materials are often used.

しかし、マグネシア質耐火材は鋼及びスラグのf%透が
大きく、構造スポールを生じ易いこトカ欠点となつ−C
おり、か\る塩基性耐火材には炭素材を複合させること
により上記の欠点が改善されてきたが、炭素材の添加は
酸化による成形体の劣化を招くという問題が新たに発生
しておシ、最近ではこれらを総括し、酸化防IF及び強
度を増大せしめる目的をもって、炭素材に併せて金属粉
末を添加することが試みられている。
However, magnesia refractory materials have a large f% penetration of steel and slag, and have the disadvantage of being prone to structural spalls.
Although the above-mentioned drawbacks have been improved by combining carbon materials with basic refractory materials, a new problem has arisen in that the addition of carbon materials causes deterioration of molded products due to oxidation. Recently, attempts have been made to add metal powder to the carbon material in order to summarize these factors and increase the oxidation prevention IF and strength.

金属粉末は、選択的に酸素と反応し、耐火物表面に緻密
層を形成して酸化を防止すると共に強度を増加させる傾
向1示すが、マグネシア質を使用した塩基性キャスタブ
ルを水で練和した場合には、マグネシアスリップのpH
が11程度の強アルカリ性となり、通常手段による金R
扮末と併用すると養生中若しくは乾燥中に反応し、発熱
・発泡を起して耐火物の組織が多孔質となり、これらが
甚だしいときには亀裂や爆裂を生じ安定な成形体が得ら
れないという現象が起ってきた。一方、このような現象
の打開策として種種の化学薬品を用いてpHを調節し、
反応を抑制することにより上記の現象を防止せんとする
試みもなされだが、品温が85℃を超えるとそれらによ
る反応抑制効果は消失し、金属粉末とマグネシアスリッ
プJ:の反応を完全に止めることはできなかったのであ
る。
Metal powder tends to selectively react with oxygen and form a dense layer on the surface of refractories, preventing oxidation and increasing strength. However, when basic castable made from magnesia is mixed with water, In case, pH of magnesia slip
becomes strongly alkaline with a value of about 11, and gold R by normal means.
If used in combination with a powder, it will react during curing or drying, causing heat generation and foaming, making the structure of the refractory porous.If this is severe, cracks and explosions may occur, making it impossible to obtain a stable molded product. I woke up. On the other hand, as a way to overcome this phenomenon, various chemicals are used to adjust the pH.
Attempts have been made to prevent the above phenomenon by suppressing the reaction, but when the product temperature exceeds 85°C, the effect of suppressing the reaction disappears, and the reaction between the metal powder and magnesia slip J: is completely stopped. It was not possible.

本発明に、川【かる現況に鑑がみ、炭素伺加のマグネシ
アIg(耐火4)I(7)酸化を防止し強度を向−ヒさ
せる金属粉末の添加を、マグネシアスリップとの反応を
生起さ1(ることなく行なった塩基性耐火物を提案紺ん
と1.−Uなされたものでちり、具体的にはその表面を
rIiΦ化被膜処理した金属粉末を用いるととにより在
来の問題点を解決し、緻密でスラグ等の浸透時j1・効
果のすぐれた新規な塩基性キャスタブルを提供゛j゛る
ことを目的としている。
In view of the current situation, the present invention includes the addition of a metal powder that prevents oxidation and increases strength of magnesia Ig (refractory 4) I (7) in addition to carbon, which causes a reaction with magnesia slip. Proposal for basic refractories made without 1.-U dust, specifically using metal powder whose surface has been treated with rIiΦ coating, which solves the conventional problems. The purpose of this invention is to solve this problem and provide a new basic castable that is dense and has excellent effects when penetrating slag, etc.

以F、本発明の実施の語例を詳細に説明する。Hereinafter, examples of implementation of the present invention will be described in detail.

表面を酸化り々11へ処JI I〜だ金属粉末とけ、酸
処理又は酸化処理によす1′(而に酸化物の被膜を形成
させタモので、金属シリ−1ン、フェロシリコン、アル
ミニウム、シリコン、金属アルミニウム等の1神父d、
2 a+以上が使用でき、この中でもフェロシリコンが
有用で一般の市販品、たとえば今生興業社製OC1)力
1に■ニフエロンリコン、0CD7J11エメタシリ等
がf車用できる。
The surface is treated with oxide 11. The metal powder is melted and then subjected to acid treatment or oxidation treatment. 1 Father d of silicon, metal aluminum, etc.
2a+ or higher can be used, and among these, ferrosilicon is useful, and commercially available products such as OC1) Force 1 manufactured by Imao Kogyo Co., Ltd., Niferon Recon, 0CD7J11 Emetasiri, etc. can be used for f cars.

この表面酸化被膜処理した金属粉末の粒度としてけ:、
反応性に安定であるためには0.125朋以下のものを
使用することが好ましい。同時に添加瞬としては05〜
10重縫係でちゃ、05重14チ以下では添加した効果
が認められず、又1呻]チ廖−しでは組織劣化が激しく
且つ耐食性の低下が著しくなるのであって、添加債は、
上記の範囲にあって特に耐火材料に対して1〜5重量係
の間において好結果を得易いのである。
The particle size of the metal powder treated with this surface oxide coating is:
In order to be stable in reactivity, it is preferable to use one with a molecular weight of 0.125 or less. At the same time, the addition instant is 05~
In the case of 10-layer seams, the effect of addition is not observed for 0.5-thick and 14-thick seams or less, and for 1-thick seams, the structure deterioration is severe and the corrosion resistance is significantly reduced.
Within the above range, it is easy to obtain good results especially when the weight ratio is between 1 and 5 for fire-resistant materials.

マグネシア原料としては天然マグネシア、海水マグネシ
ア若しくは電融マグネシア等が使用でき、その使用量は
60〜98重計係である。この晴が耐火材料の60重j
t係以下では塩基性スラグに会合したときの耐食性が損
なわれ、又98屯敞係以、ヒでけスラグの浸透による構
造スポールの面から不適当である。
As the magnesia raw material, natural magnesia, seawater magnesia, fused magnesia, etc. can be used, and the amount used is 60 to 98 gm. This fine weather is 60 heavy j of fireproof material.
If it is less than t, the corrosion resistance will be impaired when combined with basic slag, and if it is more than 98 ton, it is unsuitable from the viewpoint of structural spall due to penetration of slag.

炭素原料としては、天然黒鉛、人造黒鉛若しくけ石油コ
ークス等が使用でき、添加II/′i2〜20重量%(
好ましくは3〜10屯川Sチ)である。2@惜チ以下で
は前記した炭素材添加の効果が充分でなく、20重限チ
以上では強度や耐酸化性が低下1〜、目、つ流動性が乏
しくなって好ましくない。
As the carbon raw material, natural graphite, artificial graphite, or skeined petroleum coke can be used, and the additive II/'i2 to 20% by weight (
Preferably it is 3 to 10 tons. If it is less than 2%, the effect of the carbon material addition described above will not be sufficient, and if it is more than 20%, the strength and oxidation resistance will decrease, and fluidity will become poor, which is not preferable.

また、必要に応じて炭素結合を生ぜしめるために、ピッ
チ−やフェノール樹脂等を5重駄チまで添加してもよい
。ただし5重敬チを超すと耐火材の乾燥中に亀裂や爆裂
を生ずる懸念がある。
Furthermore, pitch, phenol resin, or the like may be added up to 5 times to form carbon bonds, if necessary. However, if the temperature exceeds 5 degrees, there is a concern that cracks or explosions may occur during the drying of the refractory material.

さらに酸化防止の補助剤として0.125 rim以下
の粒度とした炭化珪素を10重量%を限度として添加す
ることが好ましい。この補助剤の添加針はlO重撒チを
超すと41食性が極端に低下するので避けるべきである
Furthermore, it is preferable to add up to 10% by weight of silicon carbide having a particle size of 0.125 rim or less as an antioxidant aid. Addition of this adjuvant should be avoided if the amount exceeds 10 ml, as eating quality will be extremely reduced.

本発明のキャスタブルにおいては、シリカ超微粉の添加
は必須でないが、流動性を向上させ緻密化を促進する/
こめに添加は有利である。シリカ超微粉としては、フェ
ロシリコン−件産時等の副産物として得られる無定形シ
リカ等が使用でき、その添加緻は5重喰多以下が有効で
ある。5重量%を超す添加tiL乾燥中に亀裂又は爆裂
を生じ易く、且つ耐食性が著しく低下する。
In the castable of the present invention, although the addition of ultrafine silica powder is not essential, it improves fluidity and promotes densification.
Addition to rice is advantageous. As the ultrafine silica powder, amorphous silica obtained as a by-product during the production of ferrosilicon, etc. can be used, and it is effective to add the silica to a concentration of 5 times or less. Addition of TiL exceeding 5% by weight tends to cause cracks or explosions during drying, and the corrosion resistance is significantly reduced.

以上の諸成分を配合し、さらKこの配合体の標学混水喰
を低Fさせ低水分鋳込を可能とするだめに、ワーカビリ
ティを損なうことなく減水効果をもたらす周知のりグニ
ンスノリンi塩等の界面活性剤を0.1〜1.0重量%
並びにこれも周知のポリアクリル酸ノーダ、リン酸ソー
ダ系等の分散剤を0.05〜0.5  重tS添加する
ことは使用時の特性を改善するために好ましい。
The above-mentioned ingredients are blended, and in order to lower the F of the standard mixed water of this compound and enable low-moisture casting, the well-known glue gunin snolin salt, etc., which has a water-reducing effect without impairing workability, etc. 0.1-1.0% by weight of surfactant
Also, it is preferable to add 0.05 to 0.5 weight tS of a well-known dispersant such as polyacrylic acid or sodium phosphate to improve the properties during use.

次に本発明における表面酸化被膜処理した金属粉末とマ
グネシアスリップとの反応性を、未処理金属の鳴合と比
較した結果は第1表に示すとおりで、表面酸化被膜処理
した金属粉はマグネシアスリップとの反応が抑止される
効果が顕著であることが判る。
Next, the reactivity of the metal powder treated with the surface oxide film and magnesia slip in the present invention was compared with that of the untreated metal, and the results are shown in Table 1. It can be seen that the effect of suppressing the reaction is remarkable.

第1表 金属粉末の状態によるマグネシアスリップとの
反応性 この比較試験におけるマグネシアミル粉の粒度しよ、0
.044 aysす、下が80チで、使用金属の粒度は
すべて0.074 a以下のものを使用した。配合は重
滑チで添加水は外掛けである。
Table 1 Reactivity with magnesia slip depending on the state of metal powder The particle size of magnesia mill powder in this comparative test is 0.
.. 044 ays, the bottom is 80 inches, and the particle size of all metals used was 0.074 a or less. The formulation is heavy slippery and the added water is added externally.

このような配合に規定の水分を添加した後、5分間混練
して供試サンプルとしだ。サンプルをビーカー内に入れ
密封した後、恒温槽内に40℃で20時間保持し、その
状態の変化を目視、検認した。その結果は第1表に示す
ように表面酸化被膜処理した金属粉末を添加した應1及
び黒2は反応が認められなかったが、未処理金属粉末を
添加した轟8〜5はすべて反応して発泡現象が認められ
た。特K A 4及びA5についてはサンプルは流動性
が消失し固化し、ていた。
After adding a specified amount of water to such a mixture, it was kneaded for 5 minutes to prepare a test sample. After placing the sample in a beaker and sealing it, it was kept in a constant temperature bath at 40°C for 20 hours, and changes in the state were visually observed and verified. As shown in Table 1, the results showed that no reaction was observed in Oku 1 and Kuro 2, which were added with metal powder treated with a surface oxide film, but all of Todoroki 8 to 5, in which untreated metal powder was added, did not react. Foaming phenomenon was observed. For special K A4 and A5, the samples lost their fluidity and solidified.

次に、この比較試験の結果に基づく実Mliの緒例を示
す。これらの実施例1〜5の配合は、第2表及び第4表
に示すとおりで、それぞれの配合の実施例によシ得られ
る成形体の物性は第8表及び第5表に示すとおりであっ
た。同時に未処理金属粉末を配合したものを比較例”l
 ”l C1dl e、 f  及びgとして配合並び
に成形体の物性を示しだ。
Next, an example of actual Mli based on the results of this comparative test will be shown. The formulations of Examples 1 to 5 are as shown in Tables 2 and 4, and the physical properties of the molded products obtained from the Examples of each formulation are as shown in Tables 8 and 5. there were. Comparative example ``l'' which also contains untreated metal powder
The composition and physical properties of the molded product are shown as ``l C1dl e, f, and g.

実施例及び比較例における物性試験における、ブロック
乾燥テストの乾燥ブロックの製造は、モルタルミキザー
にて混合した後加水混練を行なって、振動を伺加しつつ
鉄枠に流し込んだ。10時間放1f′Y後脱枠し小型の
乾燥器にて300℃で10時間乾燥した。父、酸化テス
ト用及び−膜物性測定用ピースは、万能ミキサーにて混
合した後加水混練を行なって、摂動を付加しつつ50φ
x50mg及び40 x 40 X 160 yMの型
枠に鋳込んだ。10時間放置後脱枠し、110℃の温度
雰囲気で24時間乾燥した。
In the physical property tests in Examples and Comparative Examples, dry blocks for the block drying test were produced by mixing in a mortar mixer, then adding water and kneading, and pouring into an iron frame while applying vibration. After leaving it for 10 hours, it was removed from the frame and dried at 300° C. for 10 hours in a small dryer. The pieces for oxidation tests and for measuring film physical properties were mixed in a universal mixer, then kneaded with water, and mixed with 50φ while adding perturbation.
x50mg and cast into a mold of 40 x 40 x 160 yM. After being left for 10 hours, the frame was removed and dried in an atmosphere at a temperature of 110° C. for 24 hours.

実施例1〜5は乾燥時の亀裂、膨れ或いは爆裂は皆無で
あり、表面酸化被膜処理が施されていても金属添加によ
る酸化防止効果及び焼成後強度の増大も顕著に認められ
た。
In Examples 1 to 5, there were no cracks, blisters, or explosions during drying, and even though the surface oxide coating was applied, the anti-oxidation effect and the increase in strength after firing due to the addition of metals were also observed.

以上の結果の示すごとく、実施例1〜5のものは、乾燥
時の亀裂、膨れ或すは爆裂は皆無であり、金属粉は表面
酸化被膜処理が施されていても、金属添加による酸化防
止効果及び焼成法強度の増大も、比較例3〜gのものに
対比して顕著で、すぐれた特性を示すことが確認された
のである。
As shown by the above results, Examples 1 to 5 had no cracks, blisters, or explosions during drying, and even though the metal powder was treated with a surface oxide film, the oxidation prevention by metal addition was It was confirmed that the effect and the increase in firing strength were remarkable compared to those of Comparative Examples 3 to g, and that they exhibited excellent properties.

Claims (1)

【特許請求の範囲】[Claims] 要素含有マグネシア耐火材系組成物に、表面を酸化被膜
処理した金属粉末を添加せることを特徴とする塩基性キ
ャスタブル。
A basic castable characterized by adding metal powder whose surface has been treated with an oxide film to an element-containing magnesia refractory composition.
JP57142898A 1982-08-17 1982-08-17 Basic castable Pending JPS5935068A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57142898A JPS5935068A (en) 1982-08-17 1982-08-17 Basic castable

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57142898A JPS5935068A (en) 1982-08-17 1982-08-17 Basic castable

Publications (1)

Publication Number Publication Date
JPS5935068A true JPS5935068A (en) 1984-02-25

Family

ID=15326158

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57142898A Pending JPS5935068A (en) 1982-08-17 1982-08-17 Basic castable

Country Status (1)

Country Link
JP (1) JPS5935068A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61127672A (en) * 1984-11-22 1986-06-14 川崎製鉄株式会社 Magnesia pour-in refractories
JPS61158872A (en) * 1984-12-28 1986-07-18 ハリマセラミック株式会社 Castable refractories
US4780434A (en) * 1984-10-02 1988-10-25 Toshiba Ceramics, Co., Ltd. Refractory composition
US5284808A (en) * 1990-05-14 1994-02-08 Minteq International Inc. Dry refractory composition
EP0752397A1 (en) * 1995-07-04 1997-01-08 Asahi Glass Company Ltd. Monolithic refractory composition and process for forming a furnace wall
WO2008006779A3 (en) * 2006-07-08 2008-11-13 Refratechnik Holding Gmbh Fireproof casting insert made of fireproof raw materials and fireproof casting produced from the insert

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4780434A (en) * 1984-10-02 1988-10-25 Toshiba Ceramics, Co., Ltd. Refractory composition
JPS61127672A (en) * 1984-11-22 1986-06-14 川崎製鉄株式会社 Magnesia pour-in refractories
JPS61158872A (en) * 1984-12-28 1986-07-18 ハリマセラミック株式会社 Castable refractories
JPH0478585B2 (en) * 1984-12-28 1992-12-11 Harima Ceramic Co Ltd
US5284808A (en) * 1990-05-14 1994-02-08 Minteq International Inc. Dry refractory composition
EP0752397A1 (en) * 1995-07-04 1997-01-08 Asahi Glass Company Ltd. Monolithic refractory composition and process for forming a furnace wall
WO2008006779A3 (en) * 2006-07-08 2008-11-13 Refratechnik Holding Gmbh Fireproof casting insert made of fireproof raw materials and fireproof casting produced from the insert
EP2409960A3 (en) * 2006-07-08 2012-03-14 Refratechnik Holding GmbH Container with a fire-resistant cast compound offset made of fire-resistant raw materials and fire-resistant cast compound made from the offset

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