JPS6146428B2 - - Google Patents
Info
- Publication number
- JPS6146428B2 JPS6146428B2 JP8444178A JP8444178A JPS6146428B2 JP S6146428 B2 JPS6146428 B2 JP S6146428B2 JP 8444178 A JP8444178 A JP 8444178A JP 8444178 A JP8444178 A JP 8444178A JP S6146428 B2 JPS6146428 B2 JP S6146428B2
- Authority
- JP
- Japan
- Prior art keywords
- carbonaceous
- refractories
- molding
- carbon
- good
- 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
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
- 238000000465 moulding Methods 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000004005 microsphere Substances 0.000 claims description 3
- 239000011304 carbon pitch Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000005011 phenolic resin Substances 0.000 claims 2
- 229920001568 phenolic resin Polymers 0.000 claims 2
- 229910052742 iron Inorganic materials 0.000 claims 1
- 238000004898 kneading Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000011819 refractory material Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 239000011324 bead Substances 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000003575 carbonaceous material Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 239000011823 monolithic refractory Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Ceramic Products (AREA)
Description
従来炭素質耐火物は耐食性、耐摩耗性、耐アル
カリ性、高熱伝導性などにすぐれた特長を有する
反面、その製造方法において、カーボンブラツク
と樹脂ワニスとを混練しこれを成形する際に、カ
ーボン粉末の流動性が悪く高い成形圧を必要とす
る上に溶剤を多量に必要とし、定形耐火物の成形
に大型のプレスを必要とし、特に出銑口充填材、
樋材、ラミング材などの不定形耐火物の場合には
高い成形圧を使用せねばならず作業が困難である
等の問題があつた。
本発明はアルミナ、マグネシア、ジルコン、珪
石等の骨材を使用せず、あるいは使用しても少量
用いることにより炭素質材料を主体とする溶鉱用
耐火物を製造する方法において、上記のような問
題点を解決することを目的とするものであり、カ
ーボンブラツク、ピツチその他の炭素質材料を一
旦微小球状に造粒しておき、これに樹脂ワニスを
加えて混練し、成形時の流動性の良好な耐火物を
得ることによつて、低い成形圧による炭素質耐火
物の成形を可能にしたものである。
すなわちカーボンビーズは表面が滑らかである
上に、粒度が揃つていて空気が均一に混入するの
で流動性がきわめて良く、従つてこれをカーボン
ブラツクの代わりに使用すれば、加圧成形の際に
ブリツジを形成しないので低圧成形が可能とな
り、また表面積を小さくすることができるので結
合剤や溶剤を多量に必要とせず、従つて得られた
耐火物の高温特性を向上できる上に材料コストを
節減できるのである。
本発明方法を第1表の実施例によつて更に詳述
する。本実施例に用いたカーボンビーズは、商品
名「クレカスフエア」として市販されているもの
であり、高粘性ピツチに分散剤を添加して微粒に
分散させフラツシユドライヤーで瞬間的に加熱す
ることにより微小球状に造粒したのちこれを高温
で加熱炭化したものである。テスト方法として
は、第1表の各種配合物を常温で混練し、100
Kg/cm2の成形圧で油圧プレスにより、65×114×
230mmの形状に成形し、これを100℃で5時間加熱
したのち、300℃で10時間ベーキングした。次に
ベーキングしたテストピースをコークス被覆し、
1200℃で3時間焼成した。耐食性の試験は、各テ
ストピースを25×25×200mmの棒状に切り出し、
1550℃の侵食剤(溶鉱炉スラグ)に3時間浸漬
し、反応後冷却し、熔損された寸法をもつて比較
評価した。
Conventional carbonaceous refractories have excellent characteristics such as corrosion resistance, abrasion resistance, alkali resistance, and high thermal conductivity. It has poor fluidity and requires high molding pressure and a large amount of solvent, and a large press is required to mold shaped refractories.
In the case of monolithic refractories such as gutter materials and ramming materials, high molding pressure must be used, making the work difficult. The present invention provides a method for producing refractories for smelting mainly composed of carbonaceous materials, without using aggregates such as alumina, magnesia, zircon, and silica stone, or using only a small amount of aggregates, as described above. The purpose is to solve this problem. Carbon black, pitch, and other carbonaceous materials are first granulated into microspheres, and then resin varnish is added and kneaded to improve the fluidity during molding. By obtaining a good refractory, it is possible to mold carbonaceous refractories with low molding pressure. In other words, carbon beads have a smooth surface, have a uniform particle size, and air is evenly mixed in, so they have excellent fluidity. Therefore, if they are used in place of carbon black, they will be easier to use during pressure molding. Since no bridges are formed, low-pressure molding is possible, and since the surface area can be reduced, large amounts of binders and solvents are not required, thus improving the high-temperature properties of the resulting refractory and reducing material costs. It can be done. The method of the present invention will be explained in further detail by the examples shown in Table 1. The carbon beads used in this example are commercially available under the trade name "Crecas Sphere", and are made into fine particles by adding a dispersant to a highly viscous pitch, dispersing them into fine particles, and instantaneously heating them with a flash dryer. It is made by granulating into spherical shapes and then heating and carbonizing them at high temperatures. The test method was to knead the various compounds listed in Table 1 at room temperature, and
65×114× by hydraulic press with molding pressure of Kg/ cm2
It was molded into a shape of 230 mm, heated at 100°C for 5 hours, and then baked at 300°C for 10 hours. The baked test piece was then coated with coke,
It was baked at 1200°C for 3 hours. For the corrosion resistance test, each test piece was cut into a bar shape of 25 x 25 x 200 mm.
The specimens were immersed in an erosive agent (blast furnace slag) at 1550°C for 3 hours, cooled after the reaction, and evaluated by comparing the dimensions of the damage.
【表】
本実施例に使用したカーボンビーズと同じ粒度
の黒鉛を用いて同一条件でテストした結果を参考
例として示したが、通常はもつと高い成形圧で成
形されるものである。実施例1と参考例とを比較
すれば明らかなように、本発明方法による炭素質
耐火物は黒鉛100%のものより優れた特性を示し
ており、これは微小球状の炭素球粒が成形時の流
動性が良く同一粒度の黒鉛粉末よりはるかに気孔
率が低いことを示すものである。実施例2および
実施例3はカーボンビーズに少量の黒鉛粉末ある
いは骨材を加えると一層気孔率が向上して緻密質
のものが得られることを示しており、特に黒鉛を
混入した実施例2は高温領域における耐食性がき
わめて良好であり、また実施例2および3が実施
例1と比較して焼成後の圧縮強度が著しく向上し
ている点は、本発明方法において炭素球粒に少量
の黒鉛もしくは骨材を混入することが、高温特性
を向上するのにきわめて有効であることを示すも
のである。
上述のように、本発明方法によれば、従来低圧
成形が困難であつた炭素質耐火物を、一旦炭素質
材料を微小球に造粒することにより低圧成形を可
能にし、特に高温特性の良い不定形耐火物の成形
に適した炭素質耐火物の製造方法を提供し得る利
点があり、また材料が球状で表面積が小さいので
結合剤、溶剤を多量に必要としないことは実施例
と参考例を比較しても明らかであり、また球状で
あるため上記のように成形時の流動性が良い上に
不定形耐火物の充填性も良好である。また表面積
が小さいので耐酸化性も改善され、さらに炭素質
で表面が滑らかであるため溶銑との濡れが悪く耐
食性、耐摩耗性も一層向上し、また溶銑凝固後の
離型性も良い等の利点がある。[Table] The results of testing under the same conditions using graphite with the same particle size as the carbon beads used in this example are shown as a reference example, but the beads are usually molded at a higher molding pressure. As is clear from a comparison between Example 1 and the reference example, the carbonaceous refractories produced by the method of the present invention exhibit superior properties to those made of 100% graphite. This shows that it has good fluidity and a much lower porosity than graphite powder of the same particle size. Examples 2 and 3 show that when a small amount of graphite powder or aggregate is added to carbon beads, the porosity is further improved and dense particles can be obtained. The corrosion resistance in the high temperature range is extremely good, and the compressive strength after firing of Examples 2 and 3 is significantly improved compared to Example 1. In the method of the present invention, a small amount of graphite or This shows that mixing aggregate is extremely effective in improving high temperature properties. As described above, according to the method of the present invention, carbonaceous refractories, which have conventionally been difficult to be formed at low pressure, can be formed at low pressure by first granulating the carbonaceous material into microspheres, and the method has particularly good high-temperature properties. Examples and reference examples have the advantage of providing a method for manufacturing carbonaceous refractories suitable for forming monolithic refractories, and since the material is spherical and has a small surface area, large amounts of binders and solvents are not required. It is clear from the comparison that, since it is spherical, it not only has good fluidity during molding as described above, but also has good filling properties with the monolithic refractory. In addition, the small surface area improves oxidation resistance, and since the surface is carbonaceous and smooth, it does not wet easily with hot metal, further improving corrosion resistance and wear resistance, and also has good mold release properties after hot metal solidification. There are advantages.
Claims (1)
等の炭素質または炭素含有材料を微小球状に造粒
して、未炭化物質を含んでいる場合にはこれを加
熱炭化し、得られた炭素球粒にフエノール系樹脂
よりなる結合剤を加えて混練し、これを加圧成形
することを特徴とする製銑用耐火物の製造方法。1 Carbonaceous or carbon-containing materials such as carbon black, pitch, and phenolic resin are granulated into microspheres, and if they contain uncarbonized substances, they are heated and carbonized, and the resulting carbon spherules are injected with phenolic resin. A method for producing a refractory for iron making, which comprises adding a binder made of resin, kneading the mixture, and press-molding the mixture.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8444178A JPS5510475A (en) | 1978-07-10 | 1978-07-10 | Manufacture of refractories for pig iron |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8444178A JPS5510475A (en) | 1978-07-10 | 1978-07-10 | Manufacture of refractories for pig iron |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5510475A JPS5510475A (en) | 1980-01-24 |
| JPS6146428B2 true JPS6146428B2 (en) | 1986-10-14 |
Family
ID=13830670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8444178A Granted JPS5510475A (en) | 1978-07-10 | 1978-07-10 | Manufacture of refractories for pig iron |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5510475A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6440029U (en) * | 1987-09-04 | 1989-03-09 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59195515A (en) * | 1983-03-31 | 1984-11-06 | Mitsubishi Pencil Co Ltd | Manufacture of precision-molded hard carbon body |
| JPS6042212A (en) * | 1983-07-28 | 1985-03-06 | Tokai Carbon Co Ltd | Manufacture of heat resistant impermeable carbonaceous material |
-
1978
- 1978-07-10 JP JP8444178A patent/JPS5510475A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6440029U (en) * | 1987-09-04 | 1989-03-09 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5510475A (en) | 1980-01-24 |
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