JPH02285015A - Mud material for tap hole of blast furnace - Google Patents
Mud material for tap hole of blast furnaceInfo
- Publication number
- JPH02285015A JPH02285015A JP1108258A JP10825889A JPH02285015A JP H02285015 A JPH02285015 A JP H02285015A JP 1108258 A JP1108258 A JP 1108258A JP 10825889 A JP10825889 A JP 10825889A JP H02285015 A JPH02285015 A JP H02285015A
- Authority
- JP
- Japan
- Prior art keywords
- blast furnace
- mud material
- weight
- parts
- graphite
- 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
- 239000000463 material Substances 0.000 title claims abstract description 15
- 239000004927 clay Substances 0.000 claims abstract description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 8
- 239000010439 graphite Substances 0.000 claims abstract description 8
- 239000005995 Aluminium silicate Substances 0.000 claims abstract description 7
- 235000012211 aluminium silicate Nutrition 0.000 claims abstract description 7
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011819 refractory material Substances 0.000 claims abstract description 5
- 239000002245 particle Substances 0.000 claims description 10
- XWHPIFXRKKHEKR-UHFFFAOYSA-N iron silicon Chemical compound [Si].[Fe] XWHPIFXRKKHEKR-UHFFFAOYSA-N 0.000 claims description 6
- -1 carbon organic compounds Chemical class 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 3
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 3
- 238000004898 kneading Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 abstract description 12
- 238000005260 corrosion Methods 0.000 abstract description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 6
- 229910000519 Ferrosilicon Inorganic materials 0.000 abstract description 5
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 abstract description 5
- 229910010271 silicon carbide Inorganic materials 0.000 abstract description 5
- 239000000377 silicon dioxide Substances 0.000 abstract description 4
- 229910052681 coesite Inorganic materials 0.000 abstract description 2
- 229910052906 cristobalite Inorganic materials 0.000 abstract description 2
- 239000005011 phenolic resin Substances 0.000 abstract description 2
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 2
- 229910052682 stishovite Inorganic materials 0.000 abstract description 2
- 229910052905 tridymite Inorganic materials 0.000 abstract description 2
- 150000004767 nitrides Chemical class 0.000 abstract 2
- 239000011269 tar Substances 0.000 abstract 1
- 239000011271 tar pitch Substances 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 239000002893 slag Substances 0.000 description 10
- 238000010079 rubber tapping Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 230000007423 decrease Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 238000005245 sintering Methods 0.000 description 5
- 229910000805 Pig iron Inorganic materials 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 229910001337 iron nitride Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 230000002411 adverse Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000013003 hot bending Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052845 zircon Inorganic materials 0.000 description 2
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002829 nitrogen Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000010959 steel 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〕
この発明は高炉における出銑孔用マッド材に関するもの
である。[Detailed Description of the Invention] [Industrial Field of Application] This invention relates to a mud material for a tap hole in a blast furnace.
炉内容積(d)〕を高める努力が続けられており、出銑
比2.0以上の高炉が増えている。Efforts to increase the furnace internal volume (d) are continuing, and the number of blast furnaces with an iron tap ratio of 2.0 or higher is increasing.
この出銑比を高めるため、送風量を増加させると出銑滓
の流出速度が大きくなり、出銑孔マッド材の損傷が大き
く出銑時間の低下をきたす。また、高出銑比操業では開
孔径が小さいと、出銑初期に造銑滓速度より出銑滓速度
が小さすぎて、炉内の貯銑滓レベルが高くなり、炉内圧
の変動等を生じ、操業に悪影響を及ぼす。従って、開孔
径を大きくする必要があるが、開孔径を大きくすると出
銑時間の低下をきたす。In order to increase the tap ratio, when the air flow rate is increased, the flow rate of the tap slag increases, which causes significant damage to the tap hole mud material and reduces the tap time. In addition, in high-output ratio operations, if the opening diameter is small, the tapping slag rate is too low compared to the pig iron making rate at the early stage of tapping, and the level of stored pig iron in the furnace becomes high, causing fluctuations in the furnace pressure. , adversely affecting operations. Therefore, it is necessary to increase the opening diameter, but increasing the opening diameter causes a reduction in the tapping time.
従来の高炉出銑孔用マッド材としてはろう石、シャモッ
ト、アルミナ、炭化珪素、カーボン等の耐火骨材、耐火
粘土、金属珪素等の焼結剤並びにタール等のバインダー
からなるものが使用されている。Conventional mud materials for blast furnace tapholes include refractory aggregates such as waxite, chamotte, alumina, silicon carbide, and carbon, sintering agents such as fireclay, metal silicon, and binders such as tar. There is.
最近の鉄鋼業界では少基数の大型高炉への集約がなされ
、出銑比〔1日の出銑量(t−pigiron) /〔
発明が解決しようとする課題〕
上記、炭化珪素、カーボンは耐食性、耐摩耗性を増大さ
せるためにかなりの量が添加されるが、これ等物質は自
己焼結性がないため、添加量の増加に伴って強度が低下
する。そこで、このような強度の低下を防止するために
粘土が多量に添加されるのであるが、この粘土は高炉ス
ラグと反応し、低融物を生成する。従って、高炉スラグ
の流出に伴い出銑孔径の拡大が急激に生じ、炉内に溶銑
、溶滓を残したまま出銑が終了してしまい、出銑回数の
増加、労働負荷の増大につながっていた。In recent years, the steel industry has been concentrating on large-scale blast furnaces with a small number of units, and the pig iron production ratio [daily iron production (t-pigiron) / [
Problems to be Solved by the Invention] As mentioned above, silicon carbide and carbon are added in considerable amounts to increase corrosion resistance and wear resistance, but since these substances do not have self-sintering properties, it is difficult to increase the amount added. The strength decreases accordingly. Therefore, in order to prevent such a decrease in strength, a large amount of clay is added, but this clay reacts with the blast furnace slag to produce low-melting substances. Therefore, as the blast furnace slag flows out, the diameter of the tap hole rapidly expands, and the tapping ends with hot metal and slag remaining in the furnace, leading to an increase in the number of times of tapping and an increase in labor load. Ta.
この問題を解決するために、従来は粘土量を減少させる
こと、アルミナ微粉、ジルコン微粉等を使用することが
試みられてきた。In order to solve this problem, attempts have been made to reduce the amount of clay, use fine alumina powder, fine zircon powder, etc.
しかしながら、アルミナやジルコン等では粘土量の焼結
性が得られず、実炉使用時に出銑初期の孔径拡大が大き
くなる欠点があった。However, with alumina, zircon, etc., the sinterability of the amount of clay cannot be obtained, and there is a drawback that the pore diameter expands greatly at the initial stage of tapping when the furnace is used.
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、溶銑、溶滓に対して高い耐食性を有するとともに
、大きな強度を有し、出銑孔の急激な拡大現象がないマ
ッド材を提供することを目的とする。This invention has been proposed in view of the above-mentioned conventional circumstances, and provides a mud material that has high corrosion resistance against hot metal and slag, has great strength, and does not cause rapid expansion of the tap hole. The purpose is to provide.
上記目的を達成するためにこの発明は、SiO2含有M
含有−75〜90%酸ろう石を主原料として使用し、粒
径44μm以下の黒鉛を0. 5〜4重量部と粒径44
μm以下の窒化珪素鉄15〜30重量部とカオリン粘土
5〜15重量部と残部のその他の耐火材として、炭化珪
素、コークス等の非酸化物を使用し、タール等の残炭素
有機化合物を加えて混練するようにしている。In order to achieve the above object, the present invention provides SiO2-containing M
Containing -75 to 90% acid oxalite is used as the main raw material, and graphite with a particle size of 44 μm or less is added to 0. 5 to 4 parts by weight and particle size 44
15 to 30 parts by weight of iron silicon nitride of micrometer or less, 5 to 15 parts by weight of kaolin clay, and the rest non-oxides such as silicon carbide and coke are used as other refractory materials, and residual carbon organic compounds such as tar are added. I try to knead it.
この発明に使用される窒化珪素鉄は、フェロシリコンを
窒化したものであり、Si、N4を70〜80%含有し
、残りの大部分は金属Fe及びFs3iである。この中
のSi、N、は共有結合的性質を有し本来耐酸化性が高
く、溶銑、熔融スラグに対して濡れ難いという性質を有
してい゛るが、1400℃以上の温度で徐々に分解して
窒素を放出する性質がある。この窒素はカーボンの存在
下でカオリン粘土と反応し耐火物中に固定され、マッド
材の緻密化及び耐食性が向上すると推定される。The iron silicon nitride used in this invention is nitrided ferrosilicon and contains 70 to 80% of Si and N4, with most of the remainder being metal Fe and Fs3i. Si and N among these have covalent properties and are inherently highly oxidation resistant, making them difficult to wet with hot metal and molten slag, but they gradually decompose at temperatures above 1400°C. It has the property of releasing nitrogen. It is presumed that this nitrogen reacts with kaolin clay in the presence of carbon and is fixed in the refractory, improving the densification and corrosion resistance of the mud material.
すなわち、カオリン粘土はカーボンの存在下で上記第(
11式に示すように窒素と反応しサイアロンを生じる。That is, kaolin clay has the above-mentioned (
As shown in equation 11, it reacts with nitrogen to produce sialon.
N、−*S t、N、 ・A1.O,・AzN+上記
反応により生じたサイアロンは溶銑、溶融スラグに濡れ
難く、粘土の欠点である溶融スラグと反応して低融点物
質を生じる性質がなくなり、マント材の耐食性が大きく
改良される。N, -*S t, N, ・A1. O, .AzN+ Sialon produced by the above reaction is difficult to get wet with hot metal and molten slag, and does not have the tendency of reacting with molten slag to produce low-melting substances, which is a disadvantage of clay, and greatly improves the corrosion resistance of the mantle material.
この窒化珪素鉄は44μm以下の微粉が粘土と反応しや
すく、添加量はマッド材中で15〜30重量部が適当で
ある。15重量部以下では窒素の揮散が少なく、上記粘
土と窒素の反応が充分に生じ得ない。30重量部以上で
は反応焼結強度が高くなりすぎて、開孔が困難となり不
都合である。Fine powder of silicon iron nitride of 44 μm or less easily reacts with clay, and the appropriate amount to be added is 15 to 30 parts by weight in the mud material. If it is less than 15 parts by weight, the volatilization of nitrogen is small and the reaction between the clay and nitrogen cannot occur sufficiently. If it exceeds 30 parts by weight, the reaction sintering strength becomes too high, making it difficult to form holes, which is disadvantageous.
窒化珪素鉄の粒径が44μm以上では粘土との反応が乏
しく、粘土が未反応として残るので耐食性が低下する。When the particle size of silicon iron nitride is 44 μm or more, the reaction with clay is poor and the clay remains unreacted, resulting in a decrease in corrosion resistance.
主骨材は、高炉スラグと反応して高粘性融液を生じ徐々
に損傷されるS i 02含有量75〜90%の高珪酸
ろう石が適当である。SiO□含有量が75%より少な
いと融液の粘性が下がりすぎて損耗が大きくなる。5i
Ot含有量が90%より多いと焼結不足となり、強度が
低下する。The main aggregate is suitably high silicate waxite with an S i 02 content of 75 to 90%, which reacts with blast furnace slag to form a highly viscous melt and is gradually damaged. If the SiO□ content is less than 75%, the viscosity of the melt decreases too much and wear increases. 5i
If the Ot content is more than 90%, sintering will be insufficient and the strength will decrease.
本発明では粒径44μm以下の黒鉛を使用する。In the present invention, graphite having a particle size of 44 μm or less is used.
黒鉛は上記窒素と粘土の反応を促進するものである。そ
の配合割合は0.5〜4重量部が適当であり、0.5重
量部以下では窒素との反応が充分得られず、4重量部以
上では焼結を阻害して不都合である。黒鉛の粒径は44
μm以下が好ましく、44μm以上では窒素と粘土の反
応が乏しく、粘土が未反応として残るので、耐食性が低
下する。Graphite promotes the reaction between nitrogen and clay. The appropriate blending ratio is 0.5 to 4 parts by weight; if it is less than 0.5 parts by weight, sufficient reaction with nitrogen cannot be obtained, and if it is more than 4 parts by weight, sintering is inhibited, which is disadvantageous. The particle size of graphite is 44
The thickness is preferably .mu.m or less; if the thickness is 44 .mu.m or more, the reaction between nitrogen and clay is poor and the clay remains unreacted, resulting in a decrease in corrosion resistance.
カオリン粘土は5重量部以下ではカーボン、窒素との反
応が不十分であり、15重量部を越えると未反応の粘土
が多くなりすぎて、マッド材の耐食性に悪影響を及ぼす
。If the kaolin clay is less than 5 parts by weight, the reaction with carbon and nitrogen is insufficient, and if it exceeds 15 parts by weight, there will be too much unreacted clay, which will adversely affect the corrosion resistance of the mud material.
この他、残部の耐火性物質として、炭化珪素、コークス
等の非酸化物原料、金属珪素、フェロシリコン、アルミ
ニウム粉等の添加剤等を必要に応じて使用することがで
きる。バインダーは残炭素有機化合物、例えば通常使用
されるタール、クールピッチ、フェノールレジンを使用
することができる。In addition, as the remaining refractory material, non-oxide raw materials such as silicon carbide and coke, additives such as metallic silicon, ferrosilicon, and aluminum powder, etc. can be used as necessary. As the binder, carbon-residue organic compounds such as commonly used tar, cool pitch, and phenol resin can be used.
以上の構成及び作用により、この発明のマッド材は使用
温度付近での良好な耐食性及び充分な強度を発揮し、し
かも、出銑時に低融点物質を生成しないので、低出銑比
操業時の出銑孔の急激な拡大がなくなる。Due to the above structure and function, the mud material of the present invention exhibits good corrosion resistance and sufficient strength near the operating temperature, and does not generate low melting point substances during tapping, so it Rapid expansion of the pig hole is eliminated.
00℃における)、耐食性を示したものである。(at 00°C), which shows the corrosion resistance.
この第1表からも理解できるように本願発明品は、熱間
曲げ強さ、耐食性とも従来品の比較例よりも遥かに優れ
ていることが理解できる。As can be seen from Table 1, the products of the present invention are far superior in hot bending strength and corrosion resistance to the comparative examples of conventional products.
本発明マッド材を高炉に使用したことろ、出銑中の孔径
拡大が少なく、出銑時間が従来に比して1.5倍程長く
なり、これによってマッド材の使用量及び労働負荷が低
減した。By using the mud material of the present invention in a blast furnace, there is less pore diameter expansion during tapping, and the tapping time is approximately 1.5 times longer than conventional methods, thereby reducing the amount of mud material used and labor load. did.
以下、実施例、比較例を挙げ、本発明をより一層明瞭な
ものとする。EXAMPLES Hereinafter, examples and comparative examples will be given to make the present invention even clearer.
第1表はこの発明の実施例(a) (b)及び従来製法
に係る比較品(C)の配合割合及び熱間曲げ強さ(14
第1表
〔発明の効果〕
以上説明したように、この発明はSiO□含有175〜
90%の高珪酸ろう石を主原料として、微粉部に粒径4
4μm以下の窒化珪素鉄と粒径44μm以下の黒鉛及び
粘土を組み合わせることにより、使用温度域での耐食性
、強度が充分となり、高炉におけて出銑孔の急激な拡大
を生じない利点がある。Table 1 shows the blending ratio and hot bending strength (14
Table 1 [Effects of the Invention] As explained above, this invention has SiO□ containing 175~
The main raw material is 90% high silicate waxite, and the fine powder part has a particle size of 4.
The combination of silicon iron nitride with a particle size of 4 μm or less and graphite and clay with a particle size of 44 μm or less provides sufficient corrosion resistance and strength in the operating temperature range, and has the advantage of not causing rapid expansion of the tap hole in a blast furnace.
Claims (1)
主原料として使用し、粒径44μm以下の黒鉛を0.5
〜4重量部と粒径44μm以下の窒化珪素鉄15〜30
重量部とカオリン粘土5〜15重量部とその他の残部の
耐火材と残炭素有機化合物を加えて混練したことを特徴
とする高炉出銑孔用マッド材。[Scope of Claims] [1] Highly silicate waxite with a SiO_2 content of 75 to 90% is used as the main raw material, and 0.5% of graphite with a particle size of 44 μm or less is used as the main raw material.
~4 parts by weight and 15 to 30 iron silicon nitride with a particle size of 44 μm or less
A mud material for a blast furnace taphole, characterized in that it is kneaded by adding and kneading parts by weight of kaolin clay, 5 to 15 parts by weight of other refractory materials, and residual carbon organic compounds.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1108258A JP2787951B2 (en) | 1989-04-27 | 1989-04-27 | Mud material for blast furnace taphole |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1108258A JP2787951B2 (en) | 1989-04-27 | 1989-04-27 | Mud material for blast furnace taphole |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02285015A true JPH02285015A (en) | 1990-11-22 |
| JP2787951B2 JP2787951B2 (en) | 1998-08-20 |
Family
ID=14480097
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1108258A Expired - Lifetime JP2787951B2 (en) | 1989-04-27 | 1989-04-27 | Mud material for blast furnace taphole |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2787951B2 (en) |
-
1989
- 1989-04-27 JP JP1108258A patent/JP2787951B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP2787951B2 (en) | 1998-08-20 |
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