JPH0647502B2 - High-alumina casting material - Google Patents

High-alumina casting material

Info

Publication number
JPH0647502B2
JPH0647502B2 JP1335012A JP33501289A JPH0647502B2 JP H0647502 B2 JPH0647502 B2 JP H0647502B2 JP 1335012 A JP1335012 A JP 1335012A JP 33501289 A JP33501289 A JP 33501289A JP H0647502 B2 JPH0647502 B2 JP H0647502B2
Authority
JP
Japan
Prior art keywords
weight
alumina
casting material
hours
refractory
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 - Fee Related
Application number
JP1335012A
Other languages
Japanese (ja)
Other versions
JPH03197369A (en
Inventor
隆 山村
佳久 浜崎
久夫 戸塚
幸春 田淵
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.)
Shinagawa Refractories Co Ltd
Original Assignee
Shinagawa 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 Shinagawa Refractories Co Ltd filed Critical Shinagawa Refractories Co Ltd
Priority to JP1335012A priority Critical patent/JPH0647502B2/en
Publication of JPH03197369A publication Critical patent/JPH03197369A/en
Publication of JPH0647502B2 publication Critical patent/JPH0647502B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は耐スポーリング性に優れたハイアルミナ質流し
込み材に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial application] The present invention relates to a high-alumina casting material excellent in spalling resistance.

[従来の技術] 近年、製鋼プロセスの多様化、すなわち(1)連鋳比率の
上昇及び脱ガス比率の増加、(2)取鍋精錬の導入及び(3)
溶鋼輸送に伴う出鋼温度の上昇、溶鋼の滞留時間の延
長、溶融撹拌等により取鍋の内張り耐火物は苛酷な使用
条件となってきた。
[Prior Art] In recent years, the diversification of steelmaking processes, namely (1) increase of continuous casting ratio and increase of degassing ratio, (2) introduction of ladle refining and (3)
The refractory lining on the ladle has become a severe operating condition due to the rise of the tapping temperature due to the transportation of molten steel, the extension of the residence time of molten steel, and the agitation of melting.

従来、取鍋用内張り耐火物は、ロー石質、ジルコン質が
主体であったが、上記製鋼プロセスの多様化に対しては
ハイアルミナ質耐火物が使用されている。
Conventionally, the lining refractory for ladle has been mainly made of low stone and zircon, but high alumina refractory is used for the diversification of the steel making process.

[発明が解決しようとする課題] ハイアルミナ質耐火物はロー石質耐火物、ジルコン質耐
火物に比べ、スラグの浸潤が大きく、スラグ浸潤によっ
て形成された変質層が構造的スポーリングを生じ易い欠
点を有している。
[Problems to be Solved by the Invention] High-alumina refractory has greater slag infiltration than low-rock refractory and zircon refractory, and the altered layer formed by slag infiltration easily causes structural spalling. It has drawbacks.

また、スラグ浸潤を抑制するために、カーボン、炭化珪
素等を使用することが試みられているが、酸化によりそ
の役割は充分に果たされていない。
Further, in order to suppress the slag infiltration, it has been attempted to use carbon, silicon carbide or the like, but their role is not sufficiently fulfilled by oxidation.

このため、よりスラグ浸潤の少ないハイアルミナ質耐火
物の開発が望まれている。
For this reason, development of high alumina refractory materials with less slag infiltration is desired.

[課題を解決するための手段] 本発明者らは、ハイアルミナ質流し込み材のスラグ浸潤
を抑制するために鋭意研究を行った結果、粒径0.3mm
以下のロー石質微粉を5〜20重量%使用することによ
り本発明の所期の目的を達成できることを見出した。
[Means for Solving the Problems] The inventors of the present invention have conducted diligent research to suppress the slag infiltration of the high-alumina casting material, and as a result, have a particle diameter of 0.3 mm.
It has been found that the intended purpose of the present invention can be achieved by using 5 to 20% by weight of the following loamy fine powder.

即ち、本発明は、ハイアルミナ質流し込み材において、
ハイアルミナ質原料64〜92重量%、粒径0.3mm以
下のロー石質微粉5〜20重量%、超微粉2〜8重量%
及び結合剤1〜8重量%を含有してなることを特徴とす
るハイアルミナ質流し込み材に係る。
That is, the present invention is a high-alumina casting material,
High-alumina raw material 64-92% by weight, low-grain stone powder with a particle size of 0.3 mm or less 5-20% by weight, ultrafine powder 2-8% by weight
And a high-alumina casting material containing 1 to 8% by weight of a binder.

[作用] 本発明のハイアルミナ質流し込み材に使用するロー石質
微粉の粒径は0.3mm以下である。ロー石質微粉の粒径
が0.3mmを超えると、ロー石の膨張に伴う微亀裂の発
生のため、スラグ浸潤抑制効果が少なくなるために好ま
しくない。このロー石質微粉の添加配合量は5〜20重
量%の範囲内である。この添加配合量が5重量%未満で
あると、スラグ浸潤の抑制効果が少ないために好ましく
なく、また、該添加配合量が20重量%を超えると、耐
スラグ性が低下するために好ましくない。
[Operation] The particle size of the apatite fine powder used in the high-alumina casting material of the present invention is 0.3 mm or less. If the particle size of the apatite fine powder exceeds 0.3 mm, microcracks are generated due to the expansion of the apatite, and the slag infiltration suppressing effect is reduced, which is not preferable. The addition amount of the raw stone fine powder is in the range of 5 to 20% by weight. If the addition amount is less than 5% by weight, the effect of suppressing slag infiltration is small, which is not preferable, and if the addition amount is more than 20% by weight, the slag resistance is deteriorated, which is not preferable.

本発明のハイアルミナ質流し込み材の他の成分は慣用の
ハイアルミナ質流し込み材に使用されるものであれば特
に限定されるものではなく、耐火性骨材が主原料として
配合されることは勿論、通常使用される超微粉、結合
剤、解膠剤、乾燥促進剤及び硬化調整剤等を添加配合し
てなるものである。
The other components of the high-alumina casting material of the present invention are not particularly limited as long as they are used in a conventional high-alumina casting material, and it goes without saying that a refractory aggregate is blended as a main raw material. In addition, ultrafine powder, a binder, a deflocculant, a drying accelerator, a curing modifier and the like which are usually used are added and blended.

前記耐火性骨材としては例えば電融アルミナ、焼結アル
ミナ、仮焼アルミナ、ボーキサイト、バン土頁岩、アン
ダリュサイト、シリマナイトなどのハイアルミナ質原料
を単独で、または併用して使用することができる。
As the refractory aggregate, for example, fused alumina, sintered alumina, calcined alumina, bauxite, shale shale, andalusite, high alumina raw materials such as sillimanite can be used alone or in combination. .

この耐火性骨材の添加配合量は64〜92重量%の範囲
内である。この添加配合量が64重量%未満であると、
骨材としての機能がなくなるために好ましくなく、ま
た、92重量%を超えると、ロー石微粉、結合剤等の量
が少ないので充分な組織が得られないために好ましくな
い。
The amount of the refractory aggregate added is in the range of 64-92% by weight. If the addition amount is less than 64% by weight,
It is not preferable because the function as an aggregate is lost, and when it exceeds 92% by weight, a sufficient structure cannot be obtained because the amount of the fine rock stone powder, the binder, etc. is small, which is not preferable.

前記超微粉としては粒度としては1μm以下であり、例
えば耐火粘土、シリカ超微粉、仮焼アルミナ等を使用す
ることができる。
The ultrafine powder has a particle size of 1 μm or less, and for example, refractory clay, silica ultrafine powder, calcined alumina, etc. can be used.

この超微粉の添加配合量は2〜8重量%の範囲内であ
る。この添加配合量が2重量%未満であると、充分な組
織が得られないために好ましくなく、また、8重量%を
超えると、高温での収縮が大きくなるために好ましくな
い。
The addition amount of this ultrafine powder is in the range of 2 to 8% by weight. If the addition amount is less than 2% by weight, a sufficient structure cannot be obtained, and if it exceeds 8% by weight, shrinkage at high temperature becomes large, which is not preferable.

前記結合剤としては例えばアルミナセメント、ハイアル
ミナセメント、コロイダルシリカ等を使用することがで
きる。この結合剤の添加量としては1〜8重量%の範囲
内である。この添加配合量が1重量%未満であると、充
分な強度が得られないために好ましくなく、また、8重
量%を超えると、高温での収縮が大きくなるために好ま
しくない。
As the binder, for example, alumina cement, high alumina cement, colloidal silica or the like can be used. The amount of the binder added is in the range of 1 to 8% by weight. If the addition amount is less than 1% by weight, sufficient strength cannot be obtained, and if it exceeds 8% by weight, shrinkage at high temperature becomes large, which is not preferable.

前記解膠剤としては例えばピロリン酸ソーダ、ヘキサメ
タリン酸ソーダ、メタリン酸ソーダ等のリン酸塩、リグ
ニンスルホン酸塩(パルプ廃液)、ポリカルボン酸塩等
を使用することができる。
As the deflocculant, for example, phosphates such as sodium pyrophosphate, sodium hexametaphosphate and sodium metaphosphate, lignin sulfonate (pulp waste liquor), polycarboxylate and the like can be used.

この解膠剤の添加配合量は外掛で0.01〜0.5重量
%の範囲内である。この添加配合量が0.01重量%未
満であると、充分な分散効果が得られないために好まし
くなく、また、0.5重量%を超えると、最適分散状態
が得られないために好ましくない。
The amount of the deflocculant added and compounded is in the range of 0.01 to 0.5% by weight in the external application. If the addition amount is less than 0.01% by weight, a sufficient dispersing effect cannot be obtained, and if it exceeds 0.5% by weight, the optimum dispersion state cannot be obtained, which is not preferable. .

また、前記乾燥促進剤としては例えば金属アルミニウム
等を使用することができる。
Further, as the drying accelerator, for example, metallic aluminum or the like can be used.

この乾燥促進剤の添加配合量は外掛で0〜0.5重量%
の範囲内である。この添加配合量が0.5重量%を超え
ると、発生ガスにより充分な組織が得られないために好
ましくない。
The compounding amount of this drying accelerator is 0 to 0.5% by weight on the outside.
Within the range of. If the addition amount is more than 0.5% by weight, a sufficient structure cannot be obtained due to the generated gas, which is not preferable.

また、前記硬化調整剤としては例えば硼砂、硼酸、クエ
ン酸等を使用することができる。この硬化調整剤の添加
配合量は外掛で0.01〜0.5重量%の範囲である。
添加配合量がこれらの範囲外では充分な硬化調整が期待
できないために好ましくない。
Further, as the curing modifier, for example, borax, boric acid, citric acid or the like can be used. The amount of the curing modifier added and compounded is in the range of 0.01 to 0.5% by weight.
If the addition amount is outside these ranges, sufficient curing adjustment cannot be expected, which is not preferable.

本発明のハイアルミナ質流し込み材は上記原料を単に混
合すれば作製することができる。
The high alumina cast material of the present invention can be produced by simply mixing the above raw materials.

[実施例] 以下に実施例を挙げて本発明の流し込み材を更に説明す
る。
[Examples] The casting material of the present invention will be further described below with reference to Examples.

下記の第1表に、本発明の実施例を比較例と比較して示
す。第1表に示す各配合物は所定の水を添加して混練し
た後、金枠に流込み成形し、20℃で24時間養生し、
105℃で24時間乾燥後、以下に示す各試験に供し
た。
Table 1 below shows examples of the present invention in comparison with comparative examples. Each compound shown in Table 1 was added with predetermined water, kneaded, cast into a metal frame, and cured at 20 ° C. for 24 hours,
After being dried at 105 ° C. for 24 hours, each test shown below was used.

(1)加熱後線変化率(105℃−24時間、1000℃−3時間、
1500℃−3時間):JIS R2555に準ずる (2)加熱後圧縮強さ(105℃−24時間、1000℃−3時間、
1500℃−3時間):JIS R2553に準ずる (3)加熱後見掛気孔率(105℃−24時間、1000℃−3時
間、1500℃−3時間):JIS R2205に準ずる (4)侵食試験 装置:回転ドラム侵食試験装置 試料形状:50×200×65mm 温度・時間:1650℃−30分間スラグ投入 15分↑ ↓20分 800℃ ↓ 1650℃−30分間 15分↑ ↓20分 800℃ 5サイクル スラグ:転炉スラグ(CaO/SiO2=3.65)1.2kg/サ
イクル [発明の効果] 本発明の流し込み材は従来のハイアルミナ質流し込み材
に比べロー石質微粉の使用によりスラグ浸潤が抑制され
ることにより優れた耐スポーリング性を有する。
(1) Line change rate after heating (105 ℃ -24 hours, 1000 ℃ -3 hours,
1500 ℃ -3 hours): According to JIS R2555 (2) Compressive strength after heating (105 ℃ -24 hours, 1000 ℃ -3 hours,
1500 ℃ -3 hours): According to JIS R2553 (3) Apparent porosity after heating (105 ℃ -24 hours, 1000 ℃ -3 hours, 1500 ℃ -3 hours): According to JIS R2205 (4) Corrosion test equipment: Rotating drum erosion tester Sample shape: 50 x 200 x 65 mm Temperature / time: 1650 ° C-30 minutes Slag injection 15 minutes ↑ ↓ 20 minutes 800 ° C ↓ 1650 ° C-30 minutes 15 minutes ↑ ↓ 20 minutes 800 ° C 5 cycle slag: Converter slag (CaO / SiO 2 = 3.65) 1.2 kg / cycle [Effects of the Invention] The casting material of the present invention has excellent spalling resistance as compared with the conventional high-alumina casting material because the slag infiltration is suppressed by the use of the low-calcium fine powder.

従って、最近の製鋼プロセスの多様化に対し、本発明の
ハイアルミナ質流し込み材は亀裂、剥離が少なく、安定
した耐用が得られる材質である。
Therefore, in response to the recent diversification of the steelmaking process, the high-alumina casting material of the present invention is a material which has few cracks and peelings and can be stably used.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】ハイアルミナ質流し込み材において、ハイ
アルミナ質原料64〜92重量%、粒径0.3mm以下の
ロー石質微粉5〜20重量%、超微粉2〜8重量%及び
結合剤1〜8重量%を含有してなることを特徴とするハ
イアルミナ質流し込み材。
1. A high-alumina casting material, which comprises 64-92% by weight of a high-alumina raw material, 5-20% by weight of low-grained fine powder having a particle size of 0.3 mm or less, 2-8% by weight of ultrafine powder, and a binder 1 A high-alumina casting material characterized in that the high-alumina casting material is contained.
JP1335012A 1989-12-26 1989-12-26 High-alumina casting material Expired - Fee Related JPH0647502B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1335012A JPH0647502B2 (en) 1989-12-26 1989-12-26 High-alumina casting material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1335012A JPH0647502B2 (en) 1989-12-26 1989-12-26 High-alumina casting material

Publications (2)

Publication Number Publication Date
JPH03197369A JPH03197369A (en) 1991-08-28
JPH0647502B2 true JPH0647502B2 (en) 1994-06-22

Family

ID=18283749

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1335012A Expired - Fee Related JPH0647502B2 (en) 1989-12-26 1989-12-26 High-alumina casting material

Country Status (1)

Country Link
JP (1) JPH0647502B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101973776B (en) * 2010-11-10 2012-12-12 郑州振东科技有限公司 Production method of ladle permanent liner casting material
CN107262682B (en) * 2017-06-14 2019-07-05 沈阳化工大学 The method for preparing iron and steel smelting collection slag agent and coverture using three stone tailings

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5218710A (en) * 1975-08-04 1977-02-12 Kyushu Refractories Alumina refractory materials

Also Published As

Publication number Publication date
JPH03197369A (en) 1991-08-28

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