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JPS6138155B2 - - Google Patents
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JPS6138155B2 - - Google Patents

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Publication number
JPS6138155B2
JPS6138155B2 JP54027944A JP2794479A JPS6138155B2 JP S6138155 B2 JPS6138155 B2 JP S6138155B2 JP 54027944 A JP54027944 A JP 54027944A JP 2794479 A JP2794479 A JP 2794479A JP S6138155 B2 JPS6138155 B2 JP S6138155B2
Authority
JP
Japan
Prior art keywords
weight
carbon
magnesia
casting
refractories
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
Application number
JP54027944A
Other languages
Japanese (ja)
Other versions
JPS55121975A (en
Inventor
Akira Watanabe
Tetsuya Sugimoto
Satomi Kawahara
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.)
Krosaki Harima Corp
Original Assignee
Kyushu 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 Kyushu Refractories Co Ltd filed Critical Kyushu Refractories Co Ltd
Priority to JP2794479A priority Critical patent/JPS55121975A/en
Publication of JPS55121975A publication Critical patent/JPS55121975A/en
Publication of JPS6138155B2 publication Critical patent/JPS6138155B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は炭素―マグネシア質鋳込用耐火物に関
するものである。 近年鉄鋼業界において、省力化や省エネルギー
が強く要求されるようになり、しだいに耐火れん
がにかえて、不定形耐化物の使用量が増加してい
る。不定形耐火物の中でも特に鋳込用耐火物は、
他の材料に比較して 施工が容易で熟練を要しない。 均一な施工体が得られる。 などの特徴を有するために多種用途に広く使用さ
れている。 しかして従来の鋳込用耐火物は、耐化材として
アルミナ、高アルミナ質、高けい酸質、ジルコ
ン、炭化けい素、スピネル、などの原料を、また
結合材としてはアルミナセメントを使用したもの
が多く用いられてきた。ところがこの鋳込用耐火
物におけるアルミナセメントの使用は、耐火度を
はじめ熱間特性に劣り十分な耐用性が得られない
という欠陥があり、また近年結合材としてアルミ
ナセメントの代りにリン酸塩を使用するリン酸ボ
ンド鋳込用耐火物が使用されはじめたが、アルミ
ナセメント系鋳込用耐火物に比較して硬化速度に
バラツキがあり、特に施工場所の温度の影響を受
けやすく、またかなり高価であるという欠点があ
る。 鋳込用耐火物の耐火材料としては、塩基性スラ
グに対する抵抗性や耐火特性に関して云えば、塩
基性材料特にマグネシアが好ましい。しかしマグ
ネシアは水分や酸に接触すると水和物やマグネシ
ウム塩となつて硬化し、この硬化物が加熱される
と亀裂や爆裂を起し、組織が著しく劣化するとい
う欠陥を有している。 本発明者等は鋳込用耐火物に関し、これらの欠
陥を改良すべく鋭意研究の結果、低水分で緻密な
構造体を形成することによつて長期間の使用に耐
え得る鋳込用耐火物を見出した。すなわち鋳込用
耐火物の主材としてマグネシアを使用しこれに炭
素と減水剤を添加することによつて、加熱時にお
ける亀裂や爆裂の発生を防止して緻密な構造体を
形成できること、および炭素結合形成材の使用に
より高温化で炭素結合を形成させ、強固な構造体
を形成し、その結果炭素―マグネシア質の特性を
十分に利用して長寿命の耐火物層とすることがで
きることを見出し本発明に至つたものである。 即ち、本発明の要旨とするところは、カーボン
―マグネシア質鋳込用耐火物が72〜96.9重量%の
マグネシア、2〜20重量%の炭素材料、0.1〜2.0
重量%の減水剤、および1〜6重量%の炭素結合
形成材からなることを第1の特徴とし、またこれ
らの配合物95重量%以上と5重量%以下の粘土を
加えたものからなる耐火物を第2の特徴とするも
のである。 本発明において主材とするマグネシアの原料と
しては海水マグネシアクリンカー、焼成マグネサ
イト、電融マグネシアなどがあり、その使用量は
72〜96.9重量%好ましくは80〜96.8重量%であ
る。この量が72重量%より少ない場合は塩基性ス
ラグへの抵抗性や耐火特性が損われ、また96.9重
量%より多くなると亀裂や爆裂が発生しやすくな
つて不適当である。 次に炭素材料としては天然黒鉛、人造黒鉛、石
油コークス、鋳物コークス、カーボンブラツク、
黒鉛粘土などが用いられ、その量は2〜20重量
%、好ましくは2〜15重量%である。これは炭素
材料の量が2重量%より少ないと爆裂等が発生し
やすくなるとともに炭素の特性が発揮されず、ま
た20重量%より多いと強度や耐酸化性が低下した
り、流動性が失なわれるためである。減水剤は鋳
込用耐火物の水分を少なくして緻密な構造体を形
成するために有用であり、一般に市販されている
減水効果のある化合物を使用すればよいが、好ま
しい減水剤としてはリグニンスルホン酸塩、β―
ナフタリンスルホン酸ホルマリン縮合物、高級多
価アルコールスルホン化合物などのスルホン酸系
化合物が用いられる。そして減水剤の使用量は
0.1〜2.0重量%好ましくは0.2〜1.0重量%であ
り、0.1重量%より少ない場合は添加の効果がな
く従つて緻密な構造体が得られない。また2重量
%より多く使用しても特にその効果が向上するも
のでもないから経済性の点からも好ましくない。 また、本発明でいう炭素結合形成材とは加熱に
よつて溶融し、その後炭化して炭素結合を形成で
きるような微粒状のものである。このような材料
としてはピツチ、炭素樹脂、合成樹脂(例えば熱
硬化性フエノール樹脂、フラン樹脂)、樹脂状ピ
ツチなどを使用することができ、なかでも硬化点
が100℃以上のものが特に好ましい。水の沸騰点
より低い温度領域で軟化溶融するような炭素結合
形成材では水が蒸発する際に亀裂や爆裂の原因と
なり易く好ましくない。そしてこの炭素結合形成
材の量は1〜6重量%好ましくは1〜4重量%で
ある。この量が1重量%より少ない場合は添加の
効果がなく強固な炭素結合を形成しない。また6
重量%より多くなると密度が低下したり、亀裂や
爆裂等が発生しやすくなるので好ましくない。 さらに本発明において粘土の添加は浮水性を防
止し、炭素とマグネシアの親和性を良好にして流
動性を付与する効果を与える。その添加量は5重
量%以下、好ましくは1〜3重量%である。5重
量%より多い場合は気孔率の増加、爆裂等の発生
のほか、成分的にも耐火特性や耐スラグ性が低下
するため好ましくない。そのような粘土としては
カオリン、木節粘土、水簸粘土、ベントナイトな
どが有用である。 かくして得られる本発明の炭素―マグネシア質
鋳込用耐火物は上記構成となすことにより、炭素
―マグネシア質耐火物の特徴である高耐食性、耐
スポーリング性、スラグ侵透防止などの特性を有
し、長期間の使用に耐えることができる。 また減水剤と炭素材料を使用することによつて
構造を緻密にするとともに、爆裂等の発生を防止
し、また粘土の使用は炭素材料とマグネシアの親
和性を良好にして流動性を付与し、施工性を改善
する。 さらに炭素結合形成材の使用により、高温下に
おいて強固な炭素結合部を形成するため、炭素―
マグネシア質耐火物の特性を十分に活用すること
ができるのである。本発明の鋳込用耐火物は、流
動鋳込法(流し込み)、振動鋳込法(振動成形)
によつて施工体を得るものであり、流動鋳込法は
試料に水分を加えて混練した坏土を型枠内に流し
込み養生、乾燥して施工体を得る方法であり、振
動鋳込法は水分を加えて混練した坏土を型枠内に
投入し、振動装置によつて振動を与えその後乾燥
して施工体を得る方法である。しかして本発明の
炭素―マグネシア質鋳込用耐火物は溶銑、溶鋼あ
るいはスラグなどに接触する窯炉炉壁や樋などの
ライニング材として使用される。例えば取鍋、タ
ンデイツシユ、混銑車等の内張および高炉樋、出
鋼樋などに適しているのである。 以下実施例により本発明を詳細に説明する。 実施例 1〜5 第1表に示す配合によりウエツトパンを用いて
混合したのち、水分を加えて混練した坏土を木枠
に鋳込み脱型後110℃で5時間乾燥し鋳込材を作
製した。 また同じようにして比較例1〜2の鋳込材をも
作製した。
The present invention relates to a carbon-magnesia casting refractory. In recent years, there has been a strong demand for labor and energy conservation in the steel industry, and the amount of monolithic refractories used has gradually increased in place of refractory bricks. Among monolithic refractories, especially casting refractories,
Compared to other materials, construction is easier and does not require skill. A uniform construction body can be obtained. It is widely used for a variety of purposes due to its characteristics such as: However, conventional refractories for casting use raw materials such as alumina, high alumina, high silicic acid, zircon, silicon carbide, and spinel as refractory materials, and alumina cement as a binding material. has been used a lot. However, the use of alumina cement in cast refractories has the drawback of poor fire resistance and hot properties, making it difficult to obtain sufficient durability.In addition, in recent years, phosphates have been used as a binder instead of alumina cement. Phosphate bonded refractories for casting have begun to be used, but compared to alumina cement-based refractories for casting, the curing speed varies, they are particularly susceptible to the temperature of the construction site, and they are quite expensive. It has the disadvantage of being. As the refractory material for casting refractories, basic materials, particularly magnesia, are preferred in terms of resistance to basic slag and fireproof properties. However, when magnesia comes into contact with water or acid, it hardens into hydrates or magnesium salts, and when this hardened product is heated, it cracks or explodes, resulting in significant structural deterioration. As a result of intensive research to improve these defects in cast refractories, the present inventors have developed a cast refractory that can withstand long-term use by forming a dense structure with low moisture content. I found out. In other words, by using magnesia as the main material for cast refractories and adding carbon and a water reducing agent to it, it is possible to form a dense structure by preventing cracks and explosions during heating. It was discovered that by using a bond-forming material, carbon bonds can be formed at high temperatures to form a strong structure, and as a result, it is possible to fully utilize the characteristics of carbon-magnesia to create a long-life refractory layer. This led to the present invention. That is, the gist of the present invention is that the carbon-magnesia casting refractory contains 72 to 96.9% by weight of magnesia, 2 to 20% by weight of carbon material, and 0.1 to 2.0% by weight of magnesia.
The first characteristic is that it consists of a water-reducing agent of 1% to 6% by weight and a carbon bond forming agent of 1 to 6% by weight, and also consists of a mixture of these with the addition of 95% by weight or more and 5% by weight or less of clay. It is the second characteristic of an object. Raw materials for magnesia, which is the main material used in the present invention, include seawater magnesia clinker, calcined magnesite, and fused magnesia.
72 to 96.9% by weight, preferably 80 to 96.8% by weight. If this amount is less than 72% by weight, the resistance to basic slag and fire resistance will be impaired, and if it is more than 96.9% by weight, cracks and explosions will easily occur, making it unsuitable. Next, carbon materials include natural graphite, artificial graphite, petroleum coke, foundry coke, carbon black,
Graphite clay or the like is used in an amount of 2 to 20% by weight, preferably 2 to 15% by weight. This is because if the amount of carbon material is less than 2% by weight, explosions are likely to occur and the characteristics of carbon will not be exhibited, and if it is more than 20% by weight, strength and oxidation resistance will decrease, and fluidity will be lost. It is for the sake of becoming popular. Water reducing agents are useful for reducing the water content of cast refractories to form dense structures, and generally commercially available compounds with a water reducing effect may be used, but lignin is a preferred water reducing agent. Sulfonate, β-
Sulfonic acid compounds such as naphthalene sulfonic acid formalin condensate and higher polyhydric alcohol sulfone compounds are used. And the amount of water reducing agent used is
The amount is 0.1 to 2.0% by weight, preferably 0.2 to 1.0% by weight, and if it is less than 0.1% by weight, the addition has no effect and a dense structure cannot be obtained. Further, even if the amount is used in an amount exceeding 2% by weight, the effect is not particularly improved, so it is not preferable from an economic point of view. Further, the carbon bond forming material as used in the present invention is a fine particulate material that can be melted by heating and then carbonized to form carbon bonds. As such materials, pitch, carbon resin, synthetic resin (for example, thermosetting phenolic resin, furan resin), resinous pitch, etc. can be used, and among them, those having a hardening point of 100° C. or higher are particularly preferred. A carbon bond-forming material that softens and melts at a temperature lower than the boiling point of water is undesirable because it tends to cause cracks and explosions when water evaporates. The amount of the carbon bond forming agent is 1 to 6% by weight, preferably 1 to 4% by weight. If this amount is less than 1% by weight, the addition has no effect and strong carbon bonds are not formed. Also 6
If it exceeds % by weight, the density decreases and cracks and explosions are more likely to occur, which is not preferable. Furthermore, in the present invention, the addition of clay has the effect of preventing water floating, improving the affinity between carbon and magnesia, and imparting fluidity. The amount added is 5% by weight or less, preferably 1 to 3% by weight. If it is more than 5% by weight, it is not preferable because it increases porosity, causes explosions, etc., and also deteriorates fire resistance and slag resistance. Useful examples of such clay include kaolin, kibushi clay, elutriated clay, and bentonite. The thus obtained carbon-magnesia casting refractory of the present invention has the above-mentioned structure, and thus has properties such as high corrosion resistance, spalling resistance, and prevention of slag penetration, which are characteristics of carbon-magnesia refractories. and can withstand long-term use. In addition, the use of a water reducing agent and carbon material makes the structure dense and prevents explosions, etc., and the use of clay improves the affinity between the carbon material and magnesia, giving it fluidity. Improve workability. Furthermore, by using a carbon bond forming material, a strong carbon bond is formed under high temperatures.
This allows the characteristics of magnesia refractories to be fully utilized. The refractory for casting of the present invention can be produced using the flow casting method (pouring), the vibration casting method (vibration molding)
The fluid casting method involves adding moisture to the sample and kneading the clay, pouring it into a mold, curing it, and drying it to obtain the construction object.The vibration casting method In this method, kneaded clay with added moisture is put into a formwork, vibrated by a vibrating device, and then dried to obtain a construction body. The carbon-magnesia casting refractory of the present invention is used as a lining material for furnace walls, gutters, etc. that come into contact with hot metal, molten steel, slag, etc. For example, it is suitable for the lining of ladles, tundishes, pig iron mixers, etc., as well as for blast furnace troughs, tapping troughs, etc. The present invention will be explained in detail below with reference to Examples. Examples 1 to 5 After mixing using a wet pan according to the formulation shown in Table 1, the kneaded clay with water added thereto was cast into a wooden frame, removed from the mold, and dried at 110°C for 5 hours to prepare a casting material. In addition, casting materials of Comparative Examples 1 and 2 were also produced in the same manner.

【表】 得られた鋳込み材についてかさ比重、見掛気孔
率などの物性および爆裂、亀裂などの有無を測定
したところ第2表の結果を得た。
[Table] Physical properties such as bulk specific gravity and apparent porosity and the presence or absence of explosions and cracks were measured for the obtained cast material, and the results shown in Table 2 were obtained.

【表】【table】

【表】 〔尚爆裂(亀裂)試験は30cm×30cm×19cmの木
枠に各試料を鋳込み2時間放置後脱型し、あらか
じめ400℃に昇温した乾燥機に投入し2時間後取
出し、爆裂および亀裂の有無を観察したものであ
る。また地金・スラグの付着量などのスラグ試験
は実施例1〜5および比較例1〜2の鋳込み材を
内装の一辺が6cmで高さが20cmに張り合わせて容
器を作製し、その中に鉄:スラグ=9.5:0.5(ス
ラグ組成:SiO2…23%、CaO…52%、Total―
FeO…11%、MnO…6%、MgO…5%)を入れ
誘導炉で溶融し、1650〜1680℃で2時間保持後溶
鋼とスラグを排出した。〕 上表から本発明の炭素―マグネシア質鋳込み用
耐火物は、従来のものに比べて爆裂、亀裂の発生
が全く認められない。地金・スラグの付着量が少
なく、耐侵食性にすぐれている。ことが実証され
た。 実施例 6 第3表に示す配合により実施例1〜5と同様の
方法で鋳込材を作製した。同じようにして比較例
3〜4の鋳込材をも作製した。得られた鋳込み材
についてかさ比重、見掛気孔率などの物性および
爆裂、各還元温度での焼成強度などを測定した結
果を第3表に示した。
[Table] [For the explosion (crack) test, each sample was cast in a wooden frame of 30cm x 30cm x 19cm, left for 2 hours, removed from the mold, placed in a dryer preheated to 400℃, taken out after 2 hours, and tested for explosion. and the presence or absence of cracks was observed. In addition, slag tests such as the adhesion amount of base metal and slag were carried out by laminating the casting materials of Examples 1 to 5 and Comparative Examples 1 to 2 to a container with an inner side of 6 cm and a height of 20 cm, and placing iron inside the container. : Slag=9.5:0.5 (Slag composition: SiO 2 ...23%, CaO...52%, Total-
FeO...11%, MnO...6%, MgO...5%) were put there and melted in an induction furnace, and after being held at 1650 to 1680°C for 2 hours, the molten steel and slag were discharged. ] From the table above, the carbon-magnesia cast refractory of the present invention shows no explosion or cracking compared to conventional refractories. It has a small amount of metal and slag attached, and has excellent corrosion resistance. This has been proven. Example 6 Casting materials were produced in the same manner as Examples 1 to 5 using the formulations shown in Table 3. Casting materials of Comparative Examples 3 and 4 were also produced in the same manner. Table 3 shows the results of measuring physical properties such as bulk specific gravity and apparent porosity, explosion strength, and firing strength at various reduction temperatures for the obtained cast material.

【表】【table】

【表】 上表から本発明の炭素―マグネシア質鋳込材は
特に高温部の圧縮強度が比較例のものに比べて大
であつた。 以上の結果本発明の炭素―マグネシア質鋳込用
耐火物は前述した溶銑、溶鋼あるいはスラグなど
に接触する窯炉炉壁や樋などのライニング材とし
て長寿命の特性を発揮し、その価値は非常に大で
ある。
[Table] From the above table, the carbon-magnesia cast material of the present invention had a higher compressive strength, especially in the high temperature section, than that of the comparative example. As a result of the above, the carbon-magnesia casting refractory of the present invention exhibits long-life characteristics as a lining material for furnace walls and gutters that come into contact with hot metal, molten steel, slag, etc., and its value is extremely high. It is large.

Claims (1)

【特許請求の範囲】 1 72〜96.9重量%のマグネシア、2〜20重量%
の炭素材料、0.1〜2.0重量%の減水剤および1〜
6重量%の炭素結合形成材からなることを特徴と
する炭素―マグネシア質鋳込用耐火物。 2 72〜96.9重量%のマグネシア、2〜20重量%
の炭素材料、0.1〜2.0重量%の減水剤および1〜
6重量%の炭素結合形成材からなる混合物95重量
%以上と5重量%以下の粘土からなることを特徴
とする炭素―マグネシア質鋳込用耐火物。
[Claims] 1 72-96.9% by weight magnesia, 2-20% by weight
of carbon material, 0.1 to 2.0% by weight of water reducing agent and 1 to 2.0% by weight of water reducing agent.
A carbon-magnesia casting refractory characterized by comprising 6% by weight of a carbon bond forming material. 2 72-96.9% by weight magnesia, 2-20% by weight
of carbon material, 0.1 to 2.0% by weight of water reducing agent and 1 to 2.0% by weight of water reducing agent.
A carbon-magnesia casting refractory characterized by comprising 95% by weight or more of a mixture of 6% by weight of a carbon bond forming material and 5% by weight or less of clay.
JP2794479A 1979-03-10 1979-03-10 Carbonnmagnesia castable refractories Granted JPS55121975A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2794479A JPS55121975A (en) 1979-03-10 1979-03-10 Carbonnmagnesia castable refractories

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2794479A JPS55121975A (en) 1979-03-10 1979-03-10 Carbonnmagnesia castable refractories

Publications (2)

Publication Number Publication Date
JPS55121975A JPS55121975A (en) 1980-09-19
JPS6138155B2 true JPS6138155B2 (en) 1986-08-27

Family

ID=12234993

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2794479A Granted JPS55121975A (en) 1979-03-10 1979-03-10 Carbonnmagnesia castable refractories

Country Status (1)

Country Link
JP (1) JPS55121975A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH024729U (en) * 1988-06-24 1990-01-12
JPH0616273A (en) * 1990-12-10 1994-01-25 Internatl Business Mach Corp <Ibm> Feeding device for sheet-form medium, which is equipped with pulley guiding type feeding belt

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH024729U (en) * 1988-06-24 1990-01-12
JPH0616273A (en) * 1990-12-10 1994-01-25 Internatl Business Mach Corp <Ibm> Feeding device for sheet-form medium, which is equipped with pulley guiding type feeding belt

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JPS55121975A (en) 1980-09-19

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