JPH04144957A - Production of magnesia with erosion resistance to slag - Google Patents
Production of magnesia with erosion resistance to slagInfo
- Publication number
- JPH04144957A JPH04144957A JP2265031A JP26503190A JPH04144957A JP H04144957 A JPH04144957 A JP H04144957A JP 2265031 A JP2265031 A JP 2265031A JP 26503190 A JP26503190 A JP 26503190A JP H04144957 A JPH04144957 A JP H04144957A
- Authority
- JP
- Japan
- Prior art keywords
- magnesia
- slag
- sintering
- granulated product
- granules
- 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
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 title claims abstract description 82
- 239000000395 magnesium oxide Substances 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 239000002893 slag Substances 0.000 title claims description 37
- 230000003628 erosive effect Effects 0.000 title claims description 4
- 238000005245 sintering Methods 0.000 claims abstract description 13
- 238000010438 heat treatment Methods 0.000 claims abstract description 3
- 239000000843 powder Substances 0.000 claims abstract description 3
- 239000008187 granular material Substances 0.000 claims description 16
- 230000007797 corrosion Effects 0.000 claims description 5
- 238000005260 corrosion Methods 0.000 claims description 5
- 238000010304 firing Methods 0.000 claims description 5
- 229910000831 Steel Inorganic materials 0.000 abstract description 5
- 239000011810 insulating material Substances 0.000 abstract description 5
- 239000010959 steel Substances 0.000 abstract description 5
- 230000000704 physical effect Effects 0.000 abstract description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- 238000001354 calcination Methods 0.000 abstract 1
- 230000000977 initiatory effect Effects 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000006104 solid solution Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 4
- 241000209094 Oryza Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000010903 husk Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004453 electron probe microanalysis Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 230000009257 reactivity Effects 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〕
本発明は鉄鋼の製造工程において取り鍋及びタンデイシ
ュ内で保温材として用いられる耐スラグ浸蝕性マグネシ
アの製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for producing slag-resistant magnesia, which is used as a heat insulating material in ladles and tundishes in steel manufacturing processes.
従来、取り鍋及びタンデイシュ内の溶融金属のための保
温材並びに表面被覆材としては、焼籾殻及びマグネシア
の造粒物が広くもちいられている。Conventionally, burnt rice husks and magnesia granules have been widely used as heat insulating materials and surface coating materials for molten metal in ladles and tundishes.
しかしながら、焼き籾殻は高純度の製網を必要とする場
合、鋼に対して不純物とされているシリカ、カーボンブ
ランクを多量に含んでいる上に、稲の減反等によります
ます入手困難になってきている。However, if high-purity mesh is required, burned rice husks contain large amounts of silica and carbon blank, which are considered impurities in steel, and are becoming increasingly difficult to obtain due to factors such as reduced rice acreage. There is.
また、従来のマグネシア造粒物による表面被覆材は、高
温の溶融金属の中に入るとマグネシアの小粒子が遊離し
、溶融スラグと接触するとスラグ中のシリカ、マンガン
等との反応により固溶体を生成し、マグネシア造粒物の
形状を維持できないという問題があり、その結果、生成
された固溶体はスラグ量を増大させ、鉄鋼の製造工程に
おいて取り鍋及びタンデイシュの壁面、注入ノズル等に
付着残留して操作トラブルの原因となっていた。In addition, when conventional surface coating materials made of magnesia granules enter into high-temperature molten metal, small particles of magnesia are liberated, and when they come into contact with molten slag, they react with silica, manganese, etc. in the slag to form a solid solution. However, there is a problem that the shape of magnesia granules cannot be maintained, and as a result, the generated solid solution increases the amount of slag and remains attached to the walls of ladle and tundish, injection nozzle, etc. in the steel manufacturing process. This caused operational problems.
本発明は、鉄鋼の製造工程において取り鍋及びタンデイ
シュ内の熔融金属に遊離することなく、さらにスラグに
対し非浸蝕性を有するようにしたことでスラグ量の増加
を防ぐと共に、取り鍋の断熱煉瓦を損傷せず溶融金属を
保温することのできる耐スラグ浸蝕性マグネシアの製造
方法を提供することを目的とするものである。The present invention prevents slag from being released into the molten metal in the ladle and tundish during the steel manufacturing process, and is non-corrosive to slag, thereby preventing an increase in the amount of slag and preventing the insulating bricks of the ladle from becoming loose. The object of the present invention is to provide a method for producing slag-erosion resistant magnesia that can keep molten metal warm without damaging it.
本発明によれば、上記目的は、
マグネシア造粒物をシンタリング発生温度まで加熱して
焼成する、
ことにより達成される。According to the present invention, the above object is achieved by: heating and firing the magnesia granules to a sintering generation temperature.
かかる本発明によるマグネシア焼結物は、マグネシア造
粒物同士の焼結によって粒間の隙間が少なくなり、スラ
グとの接触面積がきわめて少なくなる。その結果、スラ
グによる浸蝕作用が抑制される。In the magnesia sintered product according to the present invention, the gaps between the particles are reduced due to sintering of the magnesia granules, and the contact area with the slag is extremely reduced. As a result, the corrosive effect of slag is suppressed.
以下、添付図面にもとづき、従来例と比較しつつ本発明
の詳細な説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described in detail below with reference to the accompanying drawings and in comparison with conventional examples.
本実施例では、第1表に示される主組成のマグネシア造
粒物を焼成温度たる1400℃以上の高温で30〜60
分間焼成して得られたマグネシア焼成物を試作品とした
。In this example, magnesia granules having the main composition shown in Table 1 were heated to 30 to 60% at a high temperature of 1400°C or higher, which is the firing temperature.
A magnesia fired product obtained by firing for a minute was used as a prototype.
第1表 試作品のマグネシアの物質主組成 (Igloss:3.1%) かくして、 得られた試作品6 gを第2表に示し た物質主組成のスラグ20gの中に入れ、1600℃の 雰囲気で接触させその結果を調べた。Table 1 Main material composition of prototype magnesia (Igloss: 3.1%) Thus, Obtained prototype 6 g is shown in Table 2. Put it in 20g of slag mainly composed of the same substance and heat it at 1600℃. The results were examined by contacting them in an atmosphere.
第2表
スラグの物質主組成
一方、上記試作品と比較するために、従来の方法で得ら
れたマグネシア造粒物を比較品とし、該比較品6gを、
上記試作品の場合と同様のスラグ20gの中に入れ、1
600℃の雰囲気で接触させその結果を調べた。Table 2 Main substance composition of slag On the other hand, in order to compare with the above prototype, magnesia granules obtained by a conventional method were used as a comparative product, and 6 g of the comparative product was
Place it in 20g of slag similar to the above prototype, and
The results were examined by contacting them in an atmosphere of 600°C.
従来のマグネシア造粒物(比較品)は、溶融金属及びス
ラグと接触して反応することにより浸蝕を受けてマグネ
シア造粒物の形状が失われた。その浸蝕現象を調べてみ
るとマグネシアとスラグの界面(接触面)で進行してお
り、その浸蝕速度は界面の表面積に依存し増加する傾向
にある。これを金属顕微鏡で見ると第4図のごとく若干
の焼結は造粒物としての形状が残っている様子が認めら
れたが、粒子間の間隙が数多くありスラグとの接触面積
が大きいため短時間で浸蝕されている。Conventional magnesia granules (comparative product) were eroded by contact with molten metal and slag and reacted, resulting in the magnesia granules losing their shape. An investigation of the corrosion phenomenon shows that it progresses at the interface (contact surface) between magnesia and slag, and the erosion rate tends to increase depending on the surface area of the interface. When this was observed with a metallurgical microscope, it was observed that some sintering remained in the form of granules, as shown in Figure 4, but due to the large number of gaps between the particles and the large contact area with the slag, the sintering was short-lived. eroded by time.
次に、本実施例におけるマグネシア焼結物(試作品)に
あっては、マグネシア造粒物を焼結させることとしてい
るので、第1図にあるように従来のマグネシア焼結物表
面被覆材と比較して、高温焼結によりシンタリングが大
きく成長し粒子間隙が少なくなると共に表面積が減少し
ている。Next, in the magnesia sintered product (prototype) in this example, magnesia granules are sintered, so as shown in Figure 1, it is different from the conventional magnesia sintered surface coating material. In comparison, high-temperature sintering causes large sintering growth, fewer interparticle gaps, and a decrease in surface area.
このように十分な焼結によりシンタリングを進行させる
ことにより、表面での浸蝕反応を防ぐことができると共
に、長時間溶融金属及びスラグと接触していても断熱材
の形状を保つことができた。By advancing sintering through sufficient sintering in this way, it was possible to prevent corrosion reactions on the surface, and the insulation material was able to maintain its shape even when in contact with molten metal and slag for a long time. .
しかし、より十分なシンタリングを進行させるためには
、マグネシアの物性によってはかなりの高温が要求され
る。物理的あるいは経済的にそれが困難な場合は、同様
な物性をもっている電融マグネシア粉体をマグネシア造
粒物の表面に被覆して焼成することにより同様な結果が
得られる。However, in order to proceed with more sufficient sintering, a considerably high temperature is required depending on the physical properties of magnesia. If this is physically or economically difficult, similar results can be obtained by coating the surface of the magnesia granules with electrofused magnesia powder having similar physical properties and firing.
上述のごとくの試作品及び比較孔との比較について、さ
らに詳しく考察を加える。A more detailed discussion will be made regarding the comparison with the prototype and comparison holes as described above.
スラグに接触している試作品及び比較孔を容器に取り出
したものについて表面の様子をそれぞれ示すものが、第
2図及び第5図である。Figures 2 and 5 show the surface appearance of the prototype in contact with the slag and the comparison hole taken out into the container, respectively.
試作品(第2図)はスラグに接触しているにも拘わらず
粒状の形が保持されているが、比較孔(第5図)は造粒
物本来の形状がマグネシアとスラグとの反応により失わ
れ、固溶体を生成している。このことからも本発明によ
るマグネシア焼結物は耐スラグ反応性が優れていること
が判る。The prototype (Figure 2) retains its granular shape even though it is in contact with slag, but the comparison hole (Figure 5) shows that the original shape of the granules is due to the reaction between magnesia and slag. is lost, forming a solid solution. This also shows that the magnesia sintered product according to the present invention has excellent slag reactivity resistance.
次に、スラグと接触後の試作品及び比較孔の内部の断面
を金属顕微鏡及びEPMAで観察した結果、それぞれ第
3図及び第6図のごとくのものが得られた。試作品は第
3図に示すとおりスラグがマグネシアの粒子間隙中に僅
かに認められたが、マグネシア焼結物は粒状をほぼ完全
に維持しており、スラグ中のシリカとマグネシア焼結物
が反応し生成する固溶体を確認することができない。Next, the cross sections of the prototype after contact with the slag and the inside of the comparison hole were observed using a metallurgical microscope and an EPMA, and as a result, the results were obtained as shown in FIGS. 3 and 6, respectively. As shown in Figure 3, in the prototype, a small amount of slag was observed between the magnesia particles, but the magnesia sintered material maintained its granularity almost completely, indicating that the silica in the slag and the magnesia sintered material had reacted. However, it is not possible to confirm the solid solution formed.
さらに第6図に示される比較孔にあっては、マグネシア
粒子の大部分がスラグ中のシリカとの反応によりMg5
f04に化学変化し、マグネシア造粒物がスラグにより
浸蝕され、角形の固溶体を生成している。Furthermore, in the comparison hole shown in FIG. 6, most of the magnesia particles react with silica in the slag, causing
A chemical change occurs at f04, and the magnesia granules are eroded by the slag, producing a square solid solution.
これらの結果から、本発明のマグネシア焼結物によるな
らば、耐スラグ浸蝕性の優れたものが得られることが確
認された。From these results, it was confirmed that the magnesia sintered product of the present invention has excellent slag corrosion resistance.
以上の結果から判明したように、本発明によるマグネシ
ア焼結物は、従来品にはなかった耐久ラグ浸蝕性を有し
ており、溶融金属の表面被覆材として用いた場合スラグ
の増加現象がなく、取り鍋等の断熱材として用いた場合
、浸蝕等による断熱材の欠損が少ないため、取り鍋使用
時間の長期化が期待できることとなった。As revealed from the above results, the magnesia sintered product according to the present invention has a durable lag corrosion property not found in conventional products, and when used as a surface coating material for molten metal, there is no increase in slag. When used as a heat insulating material for ladles, etc., the ladle can be used for a longer period of time because there is less damage to the heat insulating material due to erosion.
第1図は本発明の実施例としての試作品のスラグとの接
触後の表面を示す顕微鏡写真、第2図は上記試作品をス
ラグと共に容器内に取り出したときの表面を示す写真、
第3図は固結後に試作品をスラグと共に断面したものの
顕微鏡写真、第4図は従来品としての比較孔のスラグと
の接触後の表面を示す顕微鏡写真、第5図は上記比較孔
をスラグと共に容器内に取り出したときの表面を示す写
真、第6図は固結後に比較孔をスラグと共に断面したも
のの顕微鏡写真である。
特許出願人 訓子府石灰工業株式会社第1図
第2図
手続主甫正書(方式)
平成03年01月30日FIG. 1 is a microscopic photograph showing the surface of a prototype as an example of the present invention after it has come into contact with slag, and FIG. 2 is a photograph showing the surface of the prototype when it is taken out into a container together with slag.
Figure 3 is a microscopic photo of the cross-section of the prototype with slag after solidification, Figure 4 is a microscopic photo showing the surface of the comparison hole of a conventional product after contact with slag, and Figure 5 is a photomicrograph showing the surface of the comparison hole as a conventional product after contact with slag. FIG. 6 is a photomicrograph showing the surface of the slag taken out into the container, and FIG. 6 is a microscopic photo of the cross section of the comparison hole together with the slag after solidification. Patent Applicant Kunikofu Lime Industry Co., Ltd. Figure 1 Figure 2 Procedural Authorization (Method) January 30, 1991
Claims (2)
熱して焼成することを特徴とする耐スラグ浸蝕性マグネ
シアの製造方法。(1) A method for producing slag corrosion-resistant magnesia, which comprises heating magnesia granules to a sintering temperature and firing them.
た後に焼成することとする請求項(1)に記載の耐スラ
グ浸蝕性マグネシアの製造方法。(2) The method for producing slag erosion-resistant magnesia according to claim (1), wherein the magnesia granules are coated with electrofused magnesia powder and then fired.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2265031A JPH04144957A (en) | 1990-10-04 | 1990-10-04 | Production of magnesia with erosion resistance to slag |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2265031A JPH04144957A (en) | 1990-10-04 | 1990-10-04 | Production of magnesia with erosion resistance to slag |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04144957A true JPH04144957A (en) | 1992-05-19 |
Family
ID=17411627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2265031A Pending JPH04144957A (en) | 1990-10-04 | 1990-10-04 | Production of magnesia with erosion resistance to slag |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04144957A (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59209455A (en) * | 1983-05-11 | 1984-11-28 | Nagao Soda Kk | Heat insulating material for molten metal |
| JPS61186148A (en) * | 1985-02-13 | 1986-08-19 | Fuji Raito Kogyo Kk | Heat insulating material for molten metal |
-
1990
- 1990-10-04 JP JP2265031A patent/JPH04144957A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59209455A (en) * | 1983-05-11 | 1984-11-28 | Nagao Soda Kk | Heat insulating material for molten metal |
| JPS61186148A (en) * | 1985-02-13 | 1986-08-19 | Fuji Raito Kogyo Kk | Heat insulating material for molten metal |
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