JPS6117791B2 - - Google Patents
Info
- Publication number
- JPS6117791B2 JPS6117791B2 JP58030381A JP3038183A JPS6117791B2 JP S6117791 B2 JPS6117791 B2 JP S6117791B2 JP 58030381 A JP58030381 A JP 58030381A JP 3038183 A JP3038183 A JP 3038183A JP S6117791 B2 JPS6117791 B2 JP S6117791B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- alumina
- spray
- resistance
- furnace
- 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
- 239000000463 material Substances 0.000 claims description 36
- 239000007921 spray Substances 0.000 claims description 27
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 19
- 239000000835 fiber Substances 0.000 claims description 9
- 239000011819 refractory material Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000004927 clay Substances 0.000 claims description 6
- 229910001220 stainless steel Inorganic materials 0.000 claims description 6
- 239000010935 stainless steel Substances 0.000 claims description 6
- 239000004568 cement Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000003513 alkali Substances 0.000 description 11
- 238000005299 abrasion Methods 0.000 description 8
- 230000008439 repair process Effects 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000005507 spraying Methods 0.000 description 6
- 238000004901 spalling Methods 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920001732 Lignosulfonate Polymers 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229910000873 Beta-alumina solid electrolyte Inorganic materials 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- -1 alkali metal carboxylates Chemical class 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052850 kyanite Inorganic materials 0.000 description 1
- 239000010443 kyanite Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical class C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 239000011970 polystyrene sulfonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052851 sillimanite Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Landscapes
- Ceramic Products (AREA)
Description
本発明は、高炉炉壁の損傷部を補修する吹付材
に関するものである。
高炉は、炉寿命の末期になると炉壁耐火物の磨
耗、脱落などによつて鉄皮の赤熱、あるいは鉄皮
に亀裂が発生してガス漏れなどのトラブルが生
じ、その稼動率、操業度が低下する。
そこで最近、炉の休風時に炉内容物を減尺し、
上方開口部から挿入した吹付ノズルを用いて炉壁
の損傷個所を吹付補修することが知られている。
高炉補修には、他にも鉄皮を通して炉内部に耐火
材を圧入する方法があるが、これに比較して吹付
補修は、損傷個所、損傷度合などを確認の上で行
えることから、正確かつ効率的に補修することが
できる。本発明は、この高炉炉壁の吹付補修に好
適な吹付材を提供するものである。
転炉などの溶融金属容器においては、従来から
吹付補修が盛んに行われている。しかしながら、
高炉炉壁は炉内容物の降下にともなう磨耗、コー
クス、鉄鉱石からくるアルカリなどに対する抵抗
性、あるいは冷却効果の保持など、他の炉では見
られない特性が要求され、従来の吹付材ではこれ
に対応できなかつた。
本発明は、以上の特性を備えたものであり、ア
ルミナセメント5〜40重量%,残部がシリカ―ア
ルミナ質、高アルミナ質、アルミナ質から選ばれ
る一種又は二種以上を主材とした耐火材よりなる
配合物に、外掛けで粘土0.5〜15重量%と、ステ
ンレススチールフアイバー0.5〜10重量%を含有
した水冷クーラーを備える高炉炉壁の補修用吹付
材である。
骨材はシリカ―アルミナ質、高アルミナ質、ア
ルミナ質から選ばれる一種又は二種以上と主体と
する。これらは、従来の吹付材で使用されること
の多いマグネシア質、ドロマイト質に比較して熱
膨張率が小さく、かつ、耐熱衝撃性にすぐれるた
め、吹付材が付着した後の接着強度が高い。シリ
カ質に比較すると高融点であるとともに、耐アル
カリ性にすぐれる。さらに、材料中のアルミナ成
分は硬度が大きく、吹付材の耐磨耗性に寄力す
る。
アルミナ―シリカ質としては、カオリンや頁岩
質粘土を〓焼して得た各種のシヤモツト、あるい
はロー石など、高アルミナ質はポーキサイト、シ
リマナイト、ばん土質岩、カイアナイト、ムライ
ト、アンダリユーサイトなど、アルミナ質として
は焼結又は電融のアルミナ、あるいはK2O,
Na2Oを含有するβ―アルミナが例示される。ア
ルカリによる吹付材組織の脆弱化は、SiO2―
Al2O3成分がアルカリと反応して生じるため、上
記の耐火材のうちでもSiO2含有量の少ない高ア
ルミナ質およびアルミナ質が好ましい。
本発明では上記耐火材を主体とし、他の耐火材
を組合せてもよい。例えば炭化珪素を組合せる
と、炭化珪素がもつすぐれた耐アルカリ性と高熱
伝導性により、本発明吹付材の耐アルカリ性と熱
伝導性をさらに向上させることができる。
骨材の粒度は、充填度を勘案して粗粒、中粒、
微粒に適宜調整し、何んら限定するものではない
が、一例を示すと5〜1mm20〜70重量%,1mm以
下0〜50重量%,0.074mm以下0〜50重量%であ
る。
結合剤としてのアルミナセメントは、よく知ら
れているようにカルシユウムアルミネートを主成
分とするもので通常、180メツシユ以下の微粉を
使用し、前記耐火材に対して内掛で5〜40重量%
配合する。5重量%未満では結合剤としての効果
が十分でなく、40重量%を超えるとその分、耐火
材の割合が少なくなつて耐食性、耐磨耗性が低下
する。また耐アルカリ性の面から、SiO2成分が
0.5重量%以下のハイアルミナセメントがより好
ましい。
従来の吹付材では、結合剤としてりん酸塩、け
い酸塩などが一般的であるが、付着性などにすぐ
れている反面、強度付与に劣る。アルミナセメン
トは強度付与が他の結合剤に比べて格段にすぐ
れ、これを配合することによつて吹付材は、炉内
容物降下にともなう激しい磨耗作用に対応できる
ものである。
粘土は、炉壁に対する付着性の役割をもつ。外
掛で0.5〜20重量%,好ましくは2〜10重量%と
する。0.5重量%未満では吹付時にリバウンドロ
スが多く、補修効率が悪い。20重量%を超えると
粘土からくるSiO2成分で吹付材の耐アルカリ性
が低下し、また、粘土が微粉であるために吹付材
の粒度構成上、微粉過多となつて好ましくない。
ステンレススチールフアイバーは吹付材の熱伝
導率を向上させる。高炉は、水冷によるクーラー
で炉壁寿命の延長を図つているが、スチールフア
イバーの混入で熱伝導率が大となり、冷却作用に
よつて吹付材の耐用性が向上する。また、、一般
に高炉は外殻鉄皮内にクーラーを備えており、ク
ーラーの製造面、構造面から必然的に生じるクー
ラー間の空隙に吹付材が充填されると、スチール
フアイバーによる高熱伝導化で冷却作用が炉壁全
体に間断なく及ぶという効果がある。
ステンレススチールフアイバーは、耐スポーリ
ング性、耐磨耗性の付与と、スポーリングにより
生じた亀裂の進展を阻止し、吹付材の脱落防止と
しても大きな役割をもつ。
スチールフアイバーをステンレス材質にしたの
は、耐熱性、耐酸化性にすぐれているからであ
る。断面形状は円形、多角形のいずれでもよい。
長さは5〜50mmが好ましく、5mm未満では表面積
が小さいことにより吹付材組織の牽引支持に劣
る。50mm超えるとカーボンの沈積による体積膨張
で吹付材の亀裂発生の原因となりやすいものとと
もに、フアイバーボールが形成されやすく、作業
性の低下となる。配合量は外掛で0.5〜10重量%
とし、0.5重量%未満では配合による効果が認め
られず、10重量%を越えると吹付材の流動性が低
下してノズル詰りを生じやすい。形状はストレー
ト形の他、波形、ねじれ形、両端がふくらんだド
ツグボーン形など任意のものが使用できる。
さらに、充填性、焼結性などの向上を目的とし
て消石灰、シリカフラワー耐火性超微粉を外掛で
10重量%以下配合してもよい。また、減水効果と
親水性付与のために分散剤を3重量%以下配合し
てもよい。分散剤としてはアルカリ金属りん酸
塩、アルカリ金属ポリりん酸塩、アルカリ金属カ
ルボン酸塩、リグニンスルフオン酸塩、酢酸ビニ
ール樹脂、β―ナフタリンスルフオン酸塩、ポリ
スチレンスルフオン酸塩などがあるが、特にリグ
ニンスルフオン酸塩が効果的である。
以上からなる吹付材で高炉炉壁を補修するに
は、炉内容物の装入速度を遅くして炉内容物の水
準を降下させた後、休風し、次いで高炉炉頂の開
口部から吊下げたノズルを炉壁損傷個所へ向け、
このノズルを用いて吹付ける。吹付装置は一般に
吹付材と水とを予め混練したものを吹付ける湿式
タイプと、吹付材にノズル圧送付で水を添加して
吹付ける乾式タイプと少量の水で予じめ混練し、
さらにノズル圧送中で水を添加する半乾式とに大
別されるが、作業性の点から半乾式タイプが好ま
しい。
本発明の吹付材は、前にも述べたように水冷ク
ーラーを備えた高炉炉壁の補修用として要求され
る耐磨耗性、耐アルカリ性、耐スポーリング性お
よび高熱伝導率を兼ね備え、これをもつて補修を
行うと炉壁の寿命が著しく延長し、その結果、高
炉の稼動率、操業度を向上できる。
つぎに、本発明実施例をあげ、同時に本発明に
属しない実験例、および従来例をあげ、それぞれ
について各種特性の試験結果を示す。
The present invention relates to a spray material for repairing damaged parts of blast furnace walls. At the end of a blast furnace's life, problems such as red heat in the shell or cracks in the shell due to abrasion or falling off of the refractories on the furnace wall, such as gas leakage, occur, reducing the operating rate and efficiency of the blast furnace. descend. Therefore, recently, the contents of the furnace were reduced when the furnace was shut down.
It is known to spray repair damaged areas on the furnace wall using a spray nozzle inserted through the upper opening.
There are other methods of blast furnace repair in which refractory material is press-fitted into the furnace through the steel shell, but compared to this method, spray repair is more accurate and accurate since it can be carried out after checking the damage location and degree of damage. It can be repaired efficiently. The present invention provides a spraying material suitable for spraying repair of the blast furnace wall. BACKGROUND ART Spraying repairs have been widely used in molten metal containers such as converters. however,
Blast furnace walls are required to have properties not found in other furnaces, such as resistance to abrasion caused by the falling contents of the furnace, coke, alkali from iron ore, and retention of cooling effects. I was unable to respond to this. The present invention has the above characteristics, and is a refractory material whose main material is 5 to 40% by weight of alumina cement and the remainder is one or more selected from silica-alumina, high alumina, and alumina. This is a spraying material for repairing blast furnace walls, which is equipped with a water-cooled cooler containing 0.5 to 15% by weight of clay and 0.5 to 10% by weight of stainless steel fiber in a formulation consisting of: The aggregate is mainly one or more types selected from silica-alumina, high alumina, and alumina. These materials have a lower coefficient of thermal expansion than magnesia and dolomite materials, which are often used in conventional spray materials, and have excellent thermal shock resistance, so they have high adhesive strength after the spray materials are attached. . It has a higher melting point than siliceous materials and has excellent alkali resistance. Furthermore, the alumina component in the material has high hardness and contributes to the abrasion resistance of the spray material. Alumina-silica materials include kaolin and various types of syamoto obtained by calcining shale clay, or loite, and high alumina materials include pauxite, sillimanite, argillaceous rock, kyanite, mullite, andalyusite, etc. The quality is sintered or electrofused alumina, or K 2 O,
β-alumina containing Na 2 O is exemplified. The weakening of the spray material structure due to alkali is caused by SiO 2 ―
Since the Al 2 O 3 component is generated by reacting with an alkali, high alumina materials and alumina materials with low SiO 2 content are preferred among the above refractory materials. In the present invention, the above-mentioned refractory material is used as the main material, and other refractory materials may be used in combination. For example, when silicon carbide is used in combination, the alkali resistance and thermal conductivity of the spray material of the present invention can be further improved due to the excellent alkali resistance and high thermal conductivity of silicon carbide. The particle size of aggregate is coarse, medium, or coarse depending on the degree of filling.
The particles are suitably adjusted to fine particles, and although not limited in any way, examples include 5 to 1 mm, 20 to 70 weight %, 1 mm or less, 0 to 50 weight %, and 0.074 mm or less, 0 to 50 weight %. As is well known, alumina cement as a binder is mainly composed of calcium aluminate, and is usually used in fine powder of 180 mesh or less, and has an internal weight of 5 to 40 mesh relative to the refractory material. %
Blend. If it is less than 5% by weight, the effect as a binder is insufficient, and if it exceeds 40% by weight, the proportion of refractory material decreases accordingly, resulting in a decrease in corrosion resistance and abrasion resistance. In addition, from the standpoint of alkali resistance, the SiO 2 component is
High alumina cement of 0.5% by weight or less is more preferred. In conventional spray materials, phosphates, silicates, etc. are commonly used as binders, but while they have excellent adhesion, they are inferior in imparting strength. Alumina cement provides much better strength than other binders, and by incorporating it, the spray material can withstand the severe abrasion caused by the falling contents of the furnace. Clay has the role of adhesion to the furnace wall. The outer weight is 0.5 to 20% by weight, preferably 2 to 10% by weight. If it is less than 0.5% by weight, there will be a lot of rebound loss during spraying and the repair efficiency will be poor. If it exceeds 20% by weight, the alkali resistance of the spray material will decrease due to the SiO 2 component coming from the clay, and since the clay is a fine powder, the particle size structure of the spray material will result in an excessive amount of fine powder, which is undesirable. Stainless steel fibers improve the thermal conductivity of the spray material. Blast furnaces use water-cooled coolers to extend the life of the furnace walls, but the inclusion of steel fiber increases thermal conductivity, and the cooling effect improves the durability of the sprayed material. In addition, blast furnaces are generally equipped with a cooler inside the outer shell, and when the gap between the coolers, which inevitably arises from the manufacturing and structural aspects of the cooler, is filled with spray material, high thermal conductivity due to the steel fibers is achieved. This has the effect that the cooling effect is continuously applied to the entire furnace wall. Stainless steel fibers provide spalling and abrasion resistance, prevent the growth of cracks caused by spalling, and play an important role in preventing the spray material from falling off. The steel fiber was made of stainless steel because it has excellent heat resistance and oxidation resistance. The cross-sectional shape may be either circular or polygonal.
The length is preferably 5 to 50 mm; if it is less than 5 mm, the surface area is small and the traction support of the spray material structure is poor. If it exceeds 50 mm, volumetric expansion due to carbon deposition tends to cause cracks in the sprayed material, and fiber balls are also likely to form, reducing workability. The blending amount is 0.5 to 10% by weight.
If it is less than 0.5% by weight, no effect will be observed, and if it exceeds 10% by weight, the fluidity of the spray material will decrease and nozzle clogging will easily occur. In addition to straight shapes, any shape can be used, such as wavy, twisted, dog-bone shapes with bulges at both ends. Furthermore, in order to improve filling properties and sintering properties, slaked lime and silica flour refractory ultrafine powder are added to the outside.
It may be added in an amount of 10% by weight or less. Further, 3% by weight or less of a dispersant may be added for water reduction effect and imparting hydrophilicity. Examples of dispersants include alkali metal phosphates, alkali metal polyphosphates, alkali metal carboxylates, lignin sulfonates, vinyl acetate resins, β-naphthalene sulfonates, and polystyrene sulfonates. In particular, lignin sulfonate is effective. In order to repair the blast furnace wall with the above-mentioned spray material, the charging speed of the furnace contents is slowed down to lower the level of the furnace contents, the air is rested, and then the blast furnace is suspended from the opening at the top of the blast furnace. Aim the lowered nozzle at the damaged area of the furnace wall,
Spray using this nozzle. Spraying equipment is generally of the wet type, which sprays a mixture of spray material and water that has been mixed in advance, and the dry type, which sprays the spray material with water added to it by pressure through a nozzle.
It is further divided into a semi-dry type in which water is added during pressure feeding through a nozzle, but the semi-dry type is preferred from the viewpoint of workability. As mentioned earlier, the spray material of the present invention has the abrasion resistance, alkali resistance, spalling resistance, and high thermal conductivity required for repairing the walls of blast furnaces equipped with water-cooled coolers. If repairs are carried out, the life of the furnace wall will be significantly extended, and as a result, the operating rate and operation rate of the blast furnace can be improved. Next, examples of the present invention will be given, as well as experimental examples that do not belong to the present invention, and conventional examples, and test results of various characteristics will be shown for each.
【表】
第2表〜第4表の吹付材に含有させたステンレ
ススチールフアイバーはいずれもSUS430,巾0.5
mm×厚さ0.3mm×長さ25mmのものである。[Table] The stainless steel fibers contained in the spray materials in Tables 2 to 4 are all SUS430, width 0.5
mm x thickness 0.3mm x length 25mm.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
試験条件は次のとおりである。
(1)耐磨耗性;試料を第2表では1000℃,第3表お
よび第4表では1200℃に加熱し、サ
ンドプラスト法により測定。数値が
小さいほど耐磨耗性にすぐれる。
(2)耐アルカリ性;試料を炭酸カリウムとコークス
粉(重量比4:1)の混合物に挿入
した状態で、第2表は1200℃×5時
間を6回、第3表および第4表では
1300℃×5時間を6回くり返した
後、圧縮強さを測定した。
数値が大きいほど耐アルカリ性にす
ぐれる。
(3)耐スポーリング性;第2表は1000℃→水冷、第
3表および第4表では1300→水冷の
加熱と冷却をくり返し、試料に亀裂
が認められるまでの回数。
数値が大きいほど耐スポーリング性
にすぐれる。
(4)熱伝導率;熱線法により測定。at300℃数値が
大きいほど熱伝導率が高い。
(5)付着性;400℃に加熱した耐火物面に対して吹
付けた場合の付着率。
数値が大きいほど付着性にすぐれ
る。
(6)圧縮強さ;試料を第2表では1000℃×3時間、
第3表および第4表では1300℃×3
時間加熱した後、圧縮強さを測定。
数値が大きいほど圧縮強度が大きい。[Table] The test conditions are as follows. (1) Abrasion resistance: Samples were heated to 1000°C in Table 2 and 1200°C in Tables 3 and 4, and measured by the sandplast method. The smaller the value, the better the wear resistance. (2) Alkali resistance: Table 2 shows 1200℃ x 5 hours 6 times with the sample inserted into a mixture of potassium carbonate and coke powder (weight ratio 4:1); Tables 3 and 4 show
After repeating the test at 1300°C for 5 hours 6 times, the compressive strength was measured. The higher the number, the better the alkali resistance. (3) Spalling resistance: Table 2 shows the number of times heating and cooling is repeated from 1000°C to water cooling, and Tables 3 and 4 show the number of times heating and cooling is repeated from 1300°C to water cooling until cracks are observed in the sample. The larger the value, the better the spalling resistance. (4) Thermal conductivity; measured by hot wire method. at300℃ The larger the value, the higher the thermal conductivity. (5) Adhesion: Adhesion rate when sprayed on a refractory surface heated to 400℃. The larger the number, the better the adhesion. (6) Compressive strength;
In Tables 3 and 4, 1300℃ x 3
After heating for a time, measure the compressive strength. The larger the number, the greater the compressive strength.
Claims (1)
カ―アルミナ質、高アルミナ質、アルミナ質から
選ばれる一種又は二種以上を主材とした耐火材よ
りなる配合物に、外掛けで粘土0.5〜15重量%
と、ステンレススチールフアイバー0.5〜1.0重量
%を含有した水冷クーラーを備える高炉炉壁の補
修用吹付材。1 A mixture consisting of 5 to 40% by weight of alumina cement and the balance being a refractory material whose main material is one or more selected from silica-alumina, high alumina, and alumina, and an outer coating of 0.5 to 15% clay. weight%
A spray material for repairing blast furnace walls equipped with a water cooler containing 0.5 to 1.0% by weight of stainless steel fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58030381A JPS59156969A (en) | 1983-02-25 | 1983-02-25 | Blast furnace repairing spray material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58030381A JPS59156969A (en) | 1983-02-25 | 1983-02-25 | Blast furnace repairing spray material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59156969A JPS59156969A (en) | 1984-09-06 |
JPS6117791B2 true JPS6117791B2 (en) | 1986-05-09 |
Family
ID=12302302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58030381A Granted JPS59156969A (en) | 1983-02-25 | 1983-02-25 | Blast furnace repairing spray material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59156969A (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61127671A (en) * | 1984-11-20 | 1986-06-14 | 新日本製鐵株式会社 | Castable for spray repairing blast furnace |
US5632937A (en) * | 1991-03-22 | 1997-05-27 | Magneco/Metrel, Inc. | Method of installing a refractory lining |
CA2062697C (en) * | 1991-03-22 | 1997-04-22 | Charles W. Connors, Jr. | Method and apparatus for manufacturing and repairing molten metal containment vessels |
US5511762A (en) * | 1991-03-22 | 1996-04-30 | Magneco/Metrel, Inc. | Consumable form with degradable lining |
US5484138A (en) * | 1993-11-22 | 1996-01-16 | Magneco/Metrel, Inc. | Consumable form with adjustable walls |
CN103819211B (en) * | 2014-01-07 | 2017-06-27 | 山东耀华特耐科技有限公司 | CFBB lightweight wear-resistant plastic refractory and preparation method thereof |
JP6441684B2 (en) * | 2015-01-06 | 2018-12-19 | 新日鐵住金株式会社 | Castable refractories for lids of molten metal containers |
JP6441685B2 (en) * | 2015-01-06 | 2018-12-19 | 新日鐵住金株式会社 | Castable refractories for lids of molten metal containers |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5711878A (en) * | 1980-06-25 | 1982-01-21 | Shinagawa Refractories Co | Indefinite-form refractories |
JPS5744636A (en) * | 1980-09-01 | 1982-03-13 | Wako Chem Kk | Impregnating agent for preparing mainly semirigid or rigid resin foam |
-
1983
- 1983-02-25 JP JP58030381A patent/JPS59156969A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5711878A (en) * | 1980-06-25 | 1982-01-21 | Shinagawa Refractories Co | Indefinite-form refractories |
JPS5744636A (en) * | 1980-09-01 | 1982-03-13 | Wako Chem Kk | Impregnating agent for preparing mainly semirigid or rigid resin foam |
Also Published As
Publication number | Publication date |
---|---|
JPS59156969A (en) | 1984-09-06 |
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