JPH02160657A - Cao-containing refractory - Google Patents
Cao-containing refractoryInfo
- Publication number
- JPH02160657A JPH02160657A JP63314800A JP31480088A JPH02160657A JP H02160657 A JPH02160657 A JP H02160657A JP 63314800 A JP63314800 A JP 63314800A JP 31480088 A JP31480088 A JP 31480088A JP H02160657 A JPH02160657 A JP H02160657A
- Authority
- JP
- Japan
- Prior art keywords
- cao
- mgo
- clinker
- purity
- calcined
- 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
Links
- 239000002245 particle Substances 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 9
- 239000000292 calcium oxide Substances 0.000 abstract description 49
- 239000000395 magnesium oxide Substances 0.000 abstract description 21
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000011230 binding agent Substances 0.000 abstract description 3
- 238000005336 cracking Methods 0.000 abstract description 2
- 239000002002 slurry Substances 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 abstract 2
- 239000000347 magnesium hydroxide Substances 0.000 abstract 2
- 235000012254 magnesium hydroxide Nutrition 0.000 abstract 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 abstract 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 abstract 1
- 239000000920 calcium hydroxide Substances 0.000 abstract 1
- 235000011116 calcium hydroxide Nutrition 0.000 abstract 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 35
- 239000011449 brick Substances 0.000 description 10
- 239000011819 refractory material Substances 0.000 description 8
- 230000029087 digestion Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- 239000004568 cement Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000002893 slag Substances 0.000 description 3
- 238000004901 spalling Methods 0.000 description 3
- 238000009628 steelmaking Methods 0.000 description 3
- 102000006463 Talin Human genes 0.000 description 2
- 108010083809 Talin Proteins 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 229910019440 Mg(OH) Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000003938 response to stress Effects 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はCaO含有耐火物に関し、特にMgO−CaO
質耐火物に関する。Detailed Description of the Invention [Industrial Application Field] The present invention relates to CaO-containing refractories, particularly MgO-CaO
Regarding quality refractories.
MgO−CaO質耐火物は転炉、溶鋼鍋、セメントロー
タリーキルン等の耐火内張り材料として広く使用されて
いる。MgO-CaO refractories are widely used as refractory lining materials for converters, molten steel pots, cement rotary kilns, and the like.
MgO−CaO質耐火物の主成分であるMg0は、製鋼
スラグ、セメントキルン内のフランクス成分との反応性
が小さく浸食され難い特徴をもっているが、反面MgO
粒間の空隙はスラグ等の外来成分で満たされ易く、原れ
んが組織と外来成分の浸入を受けた部分に熱膨張率その
他の物性値の違いをもたらし、れんが内部に亀裂を発生
し易い欠点を持っている。一方、CaOは、MgOに比
べて高温下で応力に対応して変形し易い性質を持ってお
り、又製鋼スラグの主成分であるSin、、あるいは、
セメントキルン内スの主成分である5i02SKzO1
Na、01SO,といった外来成分と反応してこれらを
高融点化合物化し、れんが内部への浸入を食い止める効
果を有し、もってMgO−CaO質耐火物への亀裂導入
を抑制する作用がある。MgO, which is the main component of MgO-CaO refractories, has low reactivity with steelmaking slag and Franks components in cement kilns, making it difficult to erode.
The voids between the grains are easily filled with foreign components such as slag, which causes differences in the coefficient of thermal expansion and other physical properties between the original brick structure and the part that has been infiltrated by foreign components, resulting in the disadvantage that cracks are likely to occur inside the brick. have. On the other hand, CaO has the property of being more easily deformed in response to stress at high temperatures than MgO, and CaO, which is the main component of steelmaking slag, or
5i02SKzO1, the main component of cement kiln interior
It reacts with foreign components such as Na and 01SO to convert them into high-melting point compounds, which has the effect of preventing penetration into the interior of the brick, thereby inhibiting the introduction of cracks into the MgO--CaO refractories.
すなわち、CaOはMgO単味系耐火物の欠点である耐
熱スポーリング性あるいは耐構造スポーリング性に劣る
点をカバーする効果を有しており、両成分を組合わせる
ことによってその特性が有効に発揮されるものである。In other words, CaO has the effect of overcoming the disadvantages of single MgO refractories, which are poor heat spalling resistance and structural spalling resistance, and by combining both components, these characteristics can be effectively exhibited. It is something that will be done.
しかしながら、前述の如<CaOは高温での熱的、化学
的特性が優れる反面、常温付近の低温ではCaO+Hz
O−Ca(OH)z反応による消化現象(粉化崩壊する
)を生ずる欠点を持つことが知られている。このため、
れんが製造過程あるいは使用中にCaO含有原料がHz
Oと接触する機会があるとれんかに亀裂を生じたり、
膨張粉化現象を生じたりして、所期の目的を達成できな
いばかりか、逆に損耗速度の著しい増加をもたらす場合
さえ発生している。However, as mentioned above, while CaO has excellent thermal and chemical properties at high temperatures, at low temperatures around room temperature CaO + Hz
It is known that it has the disadvantage of causing a digestion phenomenon (pulverization and disintegration) due to the O-Ca(OH)z reaction. For this reason,
CaO-containing raw materials are exposed to Hz during the brick manufacturing process or during use.
If there is a chance of contact with O, cracks will appear in the brick,
Not only does it fail to achieve the intended purpose due to expansion and pulverization, but there are even cases where the rate of wear and tear is significantly increased.
これらのCaO含有原料を含むれんがの製造工程におい
ては、直接水と接触させることはもちろん、雰囲気中の
水蒸気、或いはバインダーその他の2次的反応によって
生成する水分にも細心の注意を払っているが、消化を完
全に防止することは著しく困難であった。In the manufacturing process of bricks containing these CaO-containing raw materials, careful attention is paid not only to direct contact with water but also to water vapor in the atmosphere or moisture generated by secondary reactions with binders and other substances. , it was extremely difficult to completely prevent digestion.
すなわち、CaO含有原料はCaO単一、またはMgO
との複合系として利用されているが、これまでの原料は
すべてCaOとMgOが均質に分布するように調整され
ている。このため、原料粒子の表面と内部のCaOとM
gOの分布状態には全く差がなく、粒表面には必ずCa
Oが露出していることになる。したがって、この粒子が
水分と接触した場合、直接CaOと水とが接触すること
になり、消化反応を生ずる。そして、粒表面の一部が消
化するだけでも膨張粉化による亀裂が粒子に発生するこ
とになり、−段と消化反応が促進され、連鎖反応的に消
化が進行する。That is, the CaO-containing raw material is CaO alone or MgO
However, all the raw materials to date have been adjusted so that CaO and MgO are homogeneously distributed. Therefore, CaO and M on the surface and inside of the raw material particles
There is no difference in the distribution state of gO, and there is always Ca on the grain surface.
This means that O is exposed. Therefore, when these particles come into contact with water, CaO and water come into direct contact, resulting in a digestive reaction. Even if only a part of the grain surface is digested, cracks will occur in the grains due to expansion and powdering, and the digestion reaction will be further accelerated and the digestion will proceed like a chain reaction.
この発明は上記従来の事情に鑑みて提案されたものであ
って、製造工程でのCaOが水分の影響を受けず、従っ
て、亀裂を生じることが少なく損耗速度の小さいCaO
含有耐火物を提供することを目的とする。This invention was proposed in view of the above-mentioned conventional circumstances, and the CaO is not affected by moisture during the manufacturing process, and therefore, CaO is less susceptible to cracking and has a lower wear rate.
The purpose is to provide refractories containing refractories.
[課題を解決するための手段〕
この発明は上記目的を達成するためにCaOとMgOを
合量で98%以上、そのうちCaO成分を5〜70%含
有し、原料粒子の表面が10〜500IImのMgO層
によって覆われているMgOCaO質タリンカーを使用
したことを特徴とするものである。[Means for Solving the Problems] In order to achieve the above object, the present invention contains a total of CaO and MgO of 98% or more, of which the CaO component is 5 to 70%, and the surface of the raw material particles is 10 to 500 II m. It is characterized by using a MgOCaO talin car covered with an MgO layer.
本発明に使用するMgO−CaO質クワクリンカー成は
CaOとMgOを合量で98%以上、望ましくは99%
以上であり、CaO成分を5〜70%、望ましくは10
〜60%とするのが良い。The MgO-CaO quaclinker composition used in the present invention has a total content of CaO and MgO of 98% or more, preferably 99%.
or more, and the CaO component is 5 to 70%, preferably 10%.
It is preferable to set it to 60%.
CaOとMgO以外の成分としては、通常Sin、、A
t、O!、Fe、O,などがあげられる。これらは比較
的低温でCaOと結合して低融点物質を形成することに
より、CaOの効果を著しく低減させるため、できるだ
け少ないことが望ましいが、1700℃以上の高温操業
下においてもMgOとCaOとの合量で98%以上あれ
ば適用可能である。Components other than CaO and MgO are usually Sin, A
T-O! , Fe, O, etc. These substances combine with CaO at relatively low temperatures to form low-melting substances, thereby significantly reducing the effect of CaO, so it is desirable to minimize the amount of these substances. It is applicable if the total amount is 98% or more.
CaO含有量は5%未満では変形により応力を緩和させ
、また、外来成分中のStowその他の成分と反応し、
充分に高融点化させることができない、また、70%を
越えると実質的に粒子表面のMgO層が10μm以下の
ものが殆どとなり、CaOの表面をMgOが十分に覆い
つくせないものも含まれるため、耐消化性の点で問題を
生ずる。When the CaO content is less than 5%, stress is relaxed by deformation, and it also reacts with Stow and other components in the foreign components,
It is not possible to raise the melting point to a sufficiently high level, and if it exceeds 70%, the MgO layer on the surface of the particles will be substantially less than 10 μm in most cases, and there are cases where the surface of CaO is not sufficiently covered by MgO. , which causes problems in terms of digestion resistance.
本発明に使用するMgO−CaO質タワタリンカ−例え
ば以下のような方法で製造したものを用いれば良い。The MgO--CaO-based linker used in the present invention may be produced, for example, by the following method.
純度99%以上のCa (OH)z及び純度98%以上
のMg(OH)zを出発原料として、Cab/MgO比
を10010〜20/80の範囲に調整したスラリーを
ロータリーキルンに投入し、1500℃〜1700℃で
焼成し1次クリンカーを作成する0次いでこの1次クリ
ンカーを2鶴〜OBに粉砕したものを非水系溶媒に分散
させた純度98%以上のM g (OH)z中に投入、
混合し、溶媒含有量10%前後まで乾燥したケーキを作
製する。Using Ca(OH)z with a purity of 99% or more and Mg(OH)z with a purity of 98% or more as starting materials, a slurry with a Cab/MgO ratio adjusted to a range of 10010 to 20/80 was charged into a rotary kiln and heated at 1500°C. Calcinate at ~1700°C to create a primary clinker.Then, this primary clinker is crushed into 2 pieces ~ OB and poured into Mg (OH) with a purity of 98% or more dispersed in a non-aqueous solvent.
Mix and make a dried cake with a solvent content of around 10%.
このケーキをロータリーキルンに投入し、1800℃以
上の温度で焼成して、得られた2次クリンカーを未粉砕
状態で篩別し、粒度骨は包装する。This cake is put into a rotary kiln and fired at a temperature of 1800° C. or higher, the resulting secondary clinker is sieved in an unpulverized state, and the granular bones are packaged.
以上のようにして製造されたMgO−CaOクリンカー
は第1図に示す如く、CaO粒子をMg0で包んだ状態
となる。それに対して第2図に示す従来のクリンカーは
CaOとMgOが均等に混じり合っているに過ぎない。The MgO--CaO clinker produced as described above has CaO particles wrapped in Mg0, as shown in FIG. On the other hand, the conventional clinker shown in FIG. 2 is simply a mixture of CaO and MgO.
本発明のCaO含有耐火物では、上記MgO−CaO質
クワクリンカー量使用しても良いし、電融マグネシア、
または焼結マグネシアを併用しても良い。In the CaO-containing refractory of the present invention, the above amount of MgO-CaO quaclinker may be used, or fused magnesia,
Alternatively, sintered magnesia may be used in combination.
本発明のCaO含有耐火物は、上記各原料にタール、液
状フェノール樹脂、ポリウレタン、ポリプロピレン、ワ
ックス等の公知の非水系バインダーを加えて混練、成形
し、焼成することによって得られる。焼成条件は特に規
定を要しないが、1600〜1700℃程度が望ましい
。The CaO-containing refractory of the present invention is obtained by adding a known non-aqueous binder such as tar, liquid phenol resin, polyurethane, polypropylene, wax, etc. to each of the above raw materials, kneading, molding, and firing. Firing conditions are not particularly specified, but are preferably about 1,600 to 1,700°C.
平均組成Mg040%、Ca059%、その他の成分1
%から成り、粒子表面層が平均厚さ約200pmのMg
O層で覆われたMgO−Ca03iクリンカーを1次タ
リンカー焼成温度1600℃、2次タリンカー焼成温度
1950℃の条件下で焼成して得た。Average composition Mg040%, Ca059%, other components 1
%, and the particle surface layer has an average thickness of about 200 pm.
A MgO-Ca03i clinker covered with an O layer was fired under conditions of a primary tallinker firing temperature of 1600°C and a secondary tallinker firing temperature of 1950°C.
本タリンカーは平均気孔率3.7%、平均がさ比重3.
17、タリン力−の最大粒径約10mの乳白色粒子であ
った。This Talinker has an average porosity of 3.7% and an average specific gravity of 3.7%.
No. 17, Talin force was a milky white particle with a maximum particle size of about 10 m.
得られたクリンカーと純度98%の海水マグネシアクリ
ンカ−を使用して第1表に示す実施例1〜3に示す焼成
MgO−CaO質れんがを製造した。Using the obtained clinker and seawater magnesia clinker with a purity of 98%, fired MgO--CaO bricks shown in Examples 1 to 3 shown in Table 1 were manufactured.
比較例
Mg041%、CaO37%、その他の成分2%から成
なる既往のMgO−CaO質タワタリンカ−純度98%
の海水マグネシアクリンカ−を使用して第1表に示す比
較例1〜3に示す焼成MgO−CaO質れんがを製造し
た。Comparative Example Existing MgO-CaO tawata linker consisting of 41% Mg, 37% CaO, and 2% other components - purity 98%
Baked MgO--CaO bricks shown in Comparative Examples 1 to 3 shown in Table 1 were manufactured using the seawater magnesia clinker.
得られたれんがの特性を第1表に併記した。The properties of the obtained bricks are also listed in Table 1.
第1表より本発明による焼成MgO−CaO貿れんが実
施例1〜3は比較例1〜3に比べていずれも著しく耐消
化性に優れるばかりでなく、耐食性、耐スポーリング性
にも優れており、製鋼炉用あるいはセメントロータリー
キルン用の耐火物として有用であることは明白である。Table 1 shows that the fired MgO-CaO trade bricks of Examples 1 to 3 according to the present invention not only have significantly better digestion resistance than Comparative Examples 1 to 3, but also have excellent corrosion resistance and spalling resistance. , it is obvious that it is useful as a refractory for steelmaking furnaces or cement rotary kilns.
第1図はこの発明に使用するMgO−CaOクリンカー
の断面図、第2図は従来のMgO−CaOの断面図であ
る。FIG. 1 is a sectional view of a MgO--CaO clinker used in the present invention, and FIG. 2 is a sectional view of a conventional MgO--CaO.
Claims (1)
aO成分を5〜70%含有し、原料粒子の表面が10〜
500μmのMgO層によって覆われているMgO−C
aO質クリンカーを使用したことを特徴とするCaO含
有耐火物。(1) The total amount of CaO and MgO is 98% or more, of which C
Contains 5 to 70% aO component, and the surface of the raw material particles is 10 to 70%.
MgO-C covered by 500μm MgO layer
A CaO-containing refractory characterized by using an aO clinker.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63314800A JPH02160657A (en) | 1988-12-12 | 1988-12-12 | Cao-containing refractory |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63314800A JPH02160657A (en) | 1988-12-12 | 1988-12-12 | Cao-containing refractory |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02160657A true JPH02160657A (en) | 1990-06-20 |
Family
ID=18057751
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63314800A Pending JPH02160657A (en) | 1988-12-12 | 1988-12-12 | Cao-containing refractory |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02160657A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007055847A (en) * | 2005-08-24 | 2007-03-08 | Itochu Ceratech Corp | Spherical calcia clinker and refractory obtained using the same |
-
1988
- 1988-12-12 JP JP63314800A patent/JPH02160657A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007055847A (en) * | 2005-08-24 | 2007-03-08 | Itochu Ceratech Corp | Spherical calcia clinker and refractory obtained using the same |
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