JP3118522B2 - Hot repair spraying material for less slag operation converter - Google Patents

Hot repair spraying material for less slag operation converter

Info

Publication number
JP3118522B2
JP3118522B2 JP04203704A JP20370492A JP3118522B2 JP 3118522 B2 JP3118522 B2 JP 3118522B2 JP 04203704 A JP04203704 A JP 04203704A JP 20370492 A JP20370492 A JP 20370492A JP 3118522 B2 JP3118522 B2 JP 3118522B2
Authority
JP
Japan
Prior art keywords
weight
less
converter
slag
hot
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 - Fee Related
Application number
JP04203704A
Other languages
Japanese (ja)
Other versions
JPH0648846A (en
Inventor
隆 山村
良介 中村
博 長岡
新太郎 須藤
俊幸 廣瀬
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shinagawa Refractories Co Ltd
Original Assignee
Shinagawa Refractories Co Ltd
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Filing date
Publication date
Application filed by Shinagawa Refractories Co Ltd filed Critical Shinagawa Refractories Co Ltd
Priority to JP04203704A priority Critical patent/JP3118522B2/en
Publication of JPH0648846A publication Critical patent/JPH0648846A/en
Application granted granted Critical
Publication of JP3118522B2 publication Critical patent/JP3118522B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/34Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing cold phosphate binders
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00482Coating or impregnation materials
    • C04B2111/00577Coating or impregnation materials applied by spraying
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/0087Uses not provided for elsewhere in C04B2111/00 for metallurgical applications
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/72Repairing or restoring existing buildings or building materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Ceramic Products (AREA)
  • Furnace Housings, Linings, Walls, And Ceilings (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、レススラグ操業を行う
ための転炉用熱間補修吹付材に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hot repair spray material for a converter for performing a less slag operation.

【0002】[0002]

【従来の技術】湿式の転炉補修吹付材として、従来から
塩基性骨材にリン酸塩を結合剤として使用し、マグネシ
アとリン酸塩との反応硬化性を利用したものが広く使用
されている。しかし、このような吹付材は硬化速度が遅
く、また、反応生成物であるリン酸マグネシアは、Mg
O・P25(融点:1165℃)、2MgO・P25(融
点:1332℃)、3MgO・P25(融点:1357
℃)のような組成を有し、融点が低く好ましいものでは
ない。
2. Description of the Related Art As a wet converter repair spraying material, a material which uses phosphate as a binder in a basic aggregate and utilizes the reaction hardening property of magnesia and phosphate has been widely used. I have. However, such a spraying material has a low curing speed, and the reaction product, magnesia phosphate, is Mg
O.P 2 O 5 (melting point: 1165 ° C.), 2MgO.P 2 O 5 (melting point: 1332 ° C.), 3MgO.P 2 O 5 (melting point: 1357)
C), and has a low melting point, which is not preferable.

【0003】また、乾式の転炉補修吹付材としては、高
耐用化のために、縮合リン酸ソーダとカルシウム化合物
とを併用して使用するのが一般的である。カルシウムを
添加することにより、付着性、接着性が顕著に向上する
原因としては、縮合リン酸塩とカルシウム化合物との反
応によるゲル化を利用して施工体を硬化させると共に高
融点であるリン酸カルシウム系化合物例えば3CaO・
25(融点=1810℃)や4CaO・P25(融点=
1720℃)を高温下で生成させて施工体に高い熱間強
度を与えることが挙げられる。
[0003] In addition, as a dry converter repair spraying material, it is common to use condensed sodium phosphate and a calcium compound in combination for high durability. The cause of the remarkable improvement in adhesion and adhesion due to the addition of calcium is that the construction body is hardened using gelation caused by the reaction between the condensed phosphate and the calcium compound, and the calcium phosphate based material having a high melting point is used. Compound such as 3CaO.
P 2 O 5 (melting point = 1810 ° C.) or 4CaO · P 2 O 5 (melting point =
(1,720 ° C.) at a high temperature to give the construction body a high hot strength.

【0004】例えば、特開昭63−156078号公報には、ド
ロマイト原料30〜70重量%とマグネシア原料70〜
30重量%とからなる耐火原料100重量部に、縮合リ
ン酸ナトリウム2.5〜7.0重量部、リンを含有しない
強電解質のアルカリ塩0.2〜1.5重量部及び難溶性リ
ン酸カルシウム0.3〜1.5重量部を含有する金属精錬
炉用吹付補修材が開示されている。
For example, Japanese Patent Application Laid-Open No. 63-156078 discloses that a dolomite raw material 30 to 70% by weight and a magnesia raw material 70 to 70% by weight are used.
100 parts by weight of a refractory raw material consisting of 30% by weight, 2.5 to 7.0 parts by weight of a condensed sodium phosphate, 0.2 to 1.5 parts by weight of an alkaline salt of a phosphorus-free strong electrolyte, and 0 A spray repair material for a metal smelting furnace containing from 0.3 to 1.5 parts by weight is disclosed.

【0005】[0005]

【発明が解決しようとする課題】従来は、吹付時の付着
性を与えるため、速硬性があり、熱間では融点ができる
だけ高い上述のような結合剤を使用した吹付材が選択さ
れていた。しかし、従来の転炉操業では、転炉内にスラ
グが多量に存在し、内張りれんが表面にもスラグが付着
しており、吹付材はこのスラグ層を介して接着してい
た。スラグ層は適度な凹凸をもち、吹付材の初期の機械
的接着を容易にし、また、高温下で吹付材の耐火材料成
分とスラグとが反応することにより、強固な接着を維持
することができるものであった。また、吹付材の損傷
も、スラグの塩基度等の影響を受けた侵食、溶損による
ものであった。従って、吹付材層はできるだけ高融点で
安定なものが好まれた。
Heretofore, a spraying material using the above-described binder which has fast curing properties and has a melting point as high as possible to be hot has been selected so as to provide adhesion during spraying. However, in the conventional converter operation, a large amount of slag was present in the converter, slag was also attached to the surface of the lining brick, and the sprayed material was bonded via this slag layer. The slag layer has moderate irregularities, facilitates the initial mechanical bonding of the sprayed material, and can maintain strong adhesion by reacting the slag with the refractory material component of the sprayed material at a high temperature. Was something. The damage to the spray material was also due to erosion and erosion affected by the slag basicity and the like. Therefore, a spraying material layer having a melting point as high as possible and stable was preferred.

【0006】ところが、近年の溶銑予備処理等の処理技
術の向上に伴い、転炉内にはスラグをできるだけ持ち込
まない、レススラグ操業が実施されるようになった。当
然転炉内には殆どスラグがなくなり、内張りれんが表面
にも、殆どスラグ付着層がなくなり、吹付材はれんが面
に直接接着しなければならなくなった。れんが面は平滑
で機械的接着は不十分であり、また、高温下でも、スラ
グとの反応による接着力維持が困難となった。従って、
レススラグ操業における吹付材の損傷はスラグによる侵
食、溶損ではなく、れんが面からの剥離によるものとな
った。
However, with the recent improvement of processing techniques such as hot metal pretreatment, less slag operation has been carried out in which slag is not brought into the converter as much as possible. Naturally, there was almost no slag in the converter, there was almost no slag adhesion layer on the surface of the lining brick, and the sprayed material had to be directly bonded to the brick surface. The brick surface was smooth and the mechanical adhesion was insufficient, and it was difficult to maintain the adhesive force by reaction with the slag even at high temperatures. Therefore,
The damage of the sprayed material in the operation of the less slag was not caused by erosion or erosion by slag but by peeling from the brick surface.

【0007】即ち、従来は結合系の融点を高くすること
により、接着強度、熱間強度を高くして吹付施工体の耐
用性を高めていたが、このような高融点結合系では、レ
ススラグ操業の転炉においては、接着強度は維持でき
ず、熱間強度のみ高い値となる。施工体は一体物として
の強度を有するが、接着力が小さいため、機械的、熱的
衝撃によりれんがとの接着面から施工体全体が一体物と
して剥離してしまう現象が現れるようになった。これ
は、ある時点までは広く残存していた吹付補修部が、あ
る時突然全くなくなってしまうことになり、補修作業を
計画的に進めることができなかった。
[0007] That is, conventionally, by increasing the melting point of the bonding system, the bonding strength and the hot strength have been increased to increase the durability of the sprayed construction. In this converter, the adhesive strength cannot be maintained, and only the hot strength becomes a high value. Although the construction body has the strength as an integral body, the phenomenon that the whole construction body is peeled off as an integral body from the bonding surface with the brick due to mechanical or thermal shock due to the small adhesive force has appeared. As a result, the spray repair part that had remained widely up to a certain point of time suddenly disappeared at one time, and the repair work could not proceed as planned.

【0008】従って、本発明の目的は、レススラグ操業
下での転炉の熱間補修においても接着強度を維持できる
熱間補修吹付材を提供することにある。
Accordingly, an object of the present invention is to provide a hot repair spraying material which can maintain the adhesive strength even during hot repair of a converter under operation of a less slag.

【0009】[0009]

【課題を解決するための手段】即ち、本発明に係るレス
スラグ操業転炉用熱間補修吹付材は、MgO質耐火材料
及びMgO−CaO質耐火材料の合計量100重量部
に、結合剤としてリン酸ソーダをP25換算で2.5〜
5.5重量%、カルシウム化合物をCaO換算で2〜6
重量%及び5μm以下の酸化マグネシウムを1.5〜4
重量%添加したことを特徴とする。
That is, the hot repair spraying material for a converter for operation of a slagless slag according to the present invention comprises a total of 100 parts by weight of a refractory material of MgO type and a refractory material of MgO-CaO type, and phosphorus as a binder. Acid soda is converted to P 2 O 5 in the range of 2.5 to 2.5.
5.5% by weight, 2-6 calcium compounds in terms of CaO
1.5 to 4% by weight of magnesium oxide of 5 μm or less.
% By weight.

【0010】[0010]

【作用】本発明の転炉用熱間補修吹付材は、MgO質耐
火材料及びMgO−CaO質耐火材料に、結合剤として
リン酸ソーダ及びカルシウム化合物に、更に5μm以下
の酸化マグネシウムを添加することによりレススラグ操
業下の転炉においても高い接着強度が得られるものであ
る。即ち、5μm以下の微細な酸化マグネシウムを添加
することにより、先ず第1に、炉内内張りれんが表面の
細かな凹凸に追従して機械的カミコミが良好となり、第
2に熱間で2MgO・P25(融点:1382℃)や3C
aO・3MgO・2P25(融点:1175℃)のような
やや融点の低い化合物を生成することによりれんが表面
に融着して高い接着力が得られるものである。
The hot repair spraying material for a converter according to the present invention is obtained by adding sodium oxide and a calcium compound as a binder to MgO refractory material and MgO-CaO refractory material, and further adding 5 μm or less of magnesium oxide. Thereby, high adhesive strength can be obtained even in a converter under operation of a less slag. That is, by adding a fine magnesium oxide of 5 μm or less, firstly, the brick inside the furnace follows the fine irregularities on the surface to improve the mechanical cracking, and secondly, 2MgO · P 2 O 5 (melting point: 1382 ° C) or 3C
By generating a compound having a slightly lower melting point such as aO.3MgO.2P 2 O 5 (melting point: 1175 ° C.), a high adhesion is obtained by fusing to a brick surface.

【0011】本発明に使用するMgO質耐火材料は、特
に限定されるものではなく、慣用の任意のものを使用で
き、例えば海水または天然マグネシアクリンカー、電融
マグネシアクリンカー等を挙げることができる。
The MgO refractory material used in the present invention is not particularly limited, and any conventional one can be used, such as seawater or natural magnesia clinker, electrofused magnesia clinker and the like.

【0012】次に、本発明に使用するMgO−CaO質
耐火材料は、MgO:CaOの重量比が85:15〜3
0:70の範囲のもの合成マグネシア・ライムクリン
ー、天然ドロマイトクリンカー等を例示することができ
る。
Next, the MgO-CaO refractory material used in the present invention has a MgO: CaO weight ratio of 85:15 to 3;
Those having a ratio of 0:70 include synthetic magnesia lime clinker, natural dolomite clinker, and the like.

【0013】本発明においては、上述のMgO質耐火材
料とMgO−CaO質耐火材料を耐火原料として使用す
る。MgO質耐火材料とMgO−CaO質耐火材料の重
量比は90:10〜30:70の範囲内である。
In the present invention, the above-mentioned MgO refractory material and MgO-CaO refractory material are used as refractory raw materials. The weight ratio between the MgO refractory material and the MgO-CaO refractory material is in the range of 90:10 to 30:70.

【0014】本発明の熱間補修吹付材においては、上述
の耐火材料の結合剤としてリン酸ソーダ、カルシウム化
合物、5μm以下の酸化マグネシウムを併用するもので
ある。ここで、リン酸ソーダとしては例えばテトラポリ
リン酸ソーダ、ヘキサメタリン酸ソーダ、トリポリリン
酸ソーダ等を使用することができる。リン酸ソーダの添
加・配合量は前記耐火材料100重量部当たりP25
算量で2.5〜5.5重量%の範囲内である。該添加・配
合量が2.5重量%未満であると初期の結合強度が不足
し、吹付直後の施工体強度が不充分であり、5.5重量
%を超えると耐食性が低下することがあり、また、経済
性の面で好ましくない。
In the hot repair spraying material of the present invention, sodium phosphate, a calcium compound and magnesium oxide of 5 μm or less are used in combination as a binder for the above-mentioned refractory material. Here, as the sodium phosphate, for example, sodium tetrapolyphosphate, sodium hexametaphosphate, sodium tripolyphosphate, or the like can be used. Adding and blending amount of sodium phosphate is in the range of 2.5 to 5.5 wt% in the refractory material per 100 parts by weight P 2 O 5 equivalent amount. If the amount added is less than 2.5% by weight, the initial bonding strength is insufficient, the strength of the construction immediately after spraying is insufficient, and if it exceeds 5.5% by weight, the corrosion resistance may decrease. Moreover, it is not preferable in terms of economy.

【0015】次に、結合剤として使用するカルシウム化
合物としては水酸化カルシウム、炭酸カルシウム、珪酸
カルシウム、アルミン酸カルシウム等を挙げることがで
きる。カルシウム化合物の添加・配合量は前記耐火材料
100重量部当たりCaO換算量で2〜6重量%の範囲
内である。該添加・配合量が2重量%未満であるとCa
O・P25系化合物の生成が少な過ぎて熱間での強度が
不充分となり、6重量%を超えると水酸化カルシウム、
炭酸カルシウムの場合、加熱された時のH2O、CO2
消失に伴う気孔の発生が多く、また、珪酸カルシウム、
アルミン酸カルシウムの場合、SiO2やAl23の不
純成分が増加してしまうので好ましくない。
Next, examples of the calcium compound used as the binder include calcium hydroxide, calcium carbonate, calcium silicate, calcium aluminate and the like. The addition and blending amount of the calcium compound is in the range of 2 to 6% by weight in terms of CaO per 100 parts by weight of the refractory material. If the amount added is less than 2% by weight, Ca
The production of the O.P 2 O 5 -based compound is too small and the hot strength becomes insufficient. If it exceeds 6% by weight, calcium hydroxide,
In the case of calcium carbonate, many pores are generated due to disappearance of H 2 O and CO 2 when heated, and calcium silicate,
Calcium aluminate is not preferred because the impurity components of SiO 2 and Al 2 O 3 increase.

【0016】更に、本発明のレススラグ操業転炉用熱間
補修吹付材には、5μm以下の酸化マグネシウムを結合
剤として使用する。酸化マグネシウムの粒度が5μmを
超えると初期の機械的カミコミが小さく、また、熱間で
の反応性に劣り、目的とする化合物を生成し難くなる。
5μm以下の酸化マグネシウムの添加・配合量は前記耐
火材料100重量部当たり1.5〜4重量%の範囲内で
ある。該添加・配合量が1.5重量%未満であると接着
強度向上効果が少なく、4重量%を超えると焼結が進み
過ぎて収縮することにより接着力が低下してくるために
好ましくない。
Further, in the hot repair spraying material for the converter for the operation of a less slag operation furnace according to the present invention, magnesium oxide of 5 μm or less is used as a binder. If the particle size of the magnesium oxide exceeds 5 μm, the mechanical mechanical stress at the initial stage is small, and the reactivity at the time of heating is inferior, so that it is difficult to produce a target compound.
The addition and blending amount of magnesium oxide of 5 μm or less is in the range of 1.5 to 4% by weight per 100 parts by weight of the refractory material. If the amount is less than 1.5% by weight, the effect of improving the adhesive strength is small, and if it exceeds 4% by weight, the sintering proceeds too much and shrinks, which is not preferred because the adhesive strength is reduced.

【0017】上述のような成分配合を有する本発明のレ
ススラグ操業転炉用熱間補修吹付材は、乾式吹付材とし
て慣用の操作によりレススラグ操業転炉の熱間補修に用
いることができる。
[0017] The hot repair spray material for the converter of the present invention having the above-mentioned composition can be used as a dry spray material for hot repair of a converter for the operation of a less slug by a conventional operation.

【0018】[0018]

【実施例】【Example】

実施例 以下の表1に示す配合割合にて本発明品及び比較品の吹
付材を作成した。得られた本発明品1〜3及び比較品の
熱間接着強度試験と加熱後接着強度試験の結果を表1に
併記する。なお、熱間接着強度試験は、1000℃のマ
グネシア・カーボン質パネルに本発明品及び比較品の吹
付材を熱間吹付けし、約5分後、接着物を剥がすための
剪断力を測定して熱間接着強度としたものである。ま
た、加熱後接着強度試験は、マグネシア・カーボン質加
熱れんが上に吹付けした試料をれんがごと1500℃で
3時間加熱処理し、冷却後吹付物を剥がすための剪断力
を測定して加熱後接着強度としたものである。
Example Spraying materials of the present invention product and the comparative product were prepared at the compounding ratios shown in Table 1 below. Table 1 also shows the results of the hot adhesive strength test and the adhesive strength test after heating of the obtained inventive products 1 to 3 and the comparative product. The hot adhesive strength test was performed by hot-spraying a spraying material of the present invention product and a comparative product on a magnesia-carbonaceous panel at 1000 ° C., and after about 5 minutes, measuring a shearing force for peeling off the adhesive. The hot adhesive strength. In addition, the adhesive strength test after heating was performed by heating the sample sprayed on the magnesia-carbonaceous heating brick together with the brick at 1500 ° C. for 3 hours, measuring the shearing force for peeling the sprayed material after cooling, and bonding after heating. It is the strength.

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【発明の効果】本発明に係るレススラグ操業転炉用熱間
補修吹付材は、結合剤としてリン酸ソーダ、カルシウム
化合物、5μm以下の酸化マグネシウムを併用したの
で、レススラグ操業でスラグのない転炉内を熱間補修す
る場合に優れた接着強度を提供することができる。
According to the present invention, since the hot repair spray material for the converter for the operation of the reslag slag according to the present invention uses sodium phosphate, a calcium compound and a magnesium oxide of 5 μm or less in combination as the binder, the converter for the reslag operation is free of slag. In the case of hot repair, excellent adhesive strength can be provided.

フロントページの続き (72)発明者 廣瀬 俊幸 東京都千代田区丸の内一丁目1番2号 日本鋼管株式会社内 (56)参考文献 特開 昭56−104781(JP,A) 特開 昭49−35409(JP,A) 特開 昭63−156078(JP,A) (58)調査した分野(Int.Cl.7,DB名) C04B 35/66 C04B 35/04 F27D 1/00 Continuation of the front page (72) Inventor Toshiyuki Hirose 1-2-1, Marunouchi, Chiyoda-ku, Tokyo Inside Nippon Kokan Co., Ltd. (56) References JP-A-56-104781 (JP, A) JP-A-49-35409 ( JP, A) JP-A-63-156078 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C04B 35/66 C04B 35/04 F27D 1/00

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 MgO質耐火材料及びMgO−CaO質
耐火材料の合計量100重量部に、結合剤としてリン酸
ソーダをP25換算で2.5〜5.5重量%、カルシウム
化合物をCaO換算で2〜6重量%及び5μm以下の酸
化マグネシウムを1.5〜4重量%添加したことを特徴
とするレススラグ操業転炉用熱間補修吹付材。
1. A total of 100 parts by weight of a MgO refractory material and a MgO-CaO refractory material, 2.5 to 5.5% by weight of sodium phosphate as a binder and a calcium compound as P 2 O 5 as a binder. A hot repair spraying material for a less slag operation converter, wherein 1.5 to 4% by weight of magnesium oxide having a CaO equivalent of 2 to 6% by weight and 5 μm or less is added.
JP04203704A 1992-07-30 1992-07-30 Hot repair spraying material for less slag operation converter Expired - Fee Related JP3118522B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04203704A JP3118522B2 (en) 1992-07-30 1992-07-30 Hot repair spraying material for less slag operation converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04203704A JP3118522B2 (en) 1992-07-30 1992-07-30 Hot repair spraying material for less slag operation converter

Publications (2)

Publication Number Publication Date
JPH0648846A JPH0648846A (en) 1994-02-22
JP3118522B2 true JP3118522B2 (en) 2000-12-18

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3118522B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE40109E1 (en) 1996-06-05 2008-02-26 Ricoh Company, Ltd. Multi-beam optical scanner
JP3895416B2 (en) * 1996-06-05 2007-03-22 株式会社リコー Multi-beam optical scanning device
WO1998048043A1 (en) * 1997-04-24 1998-10-29 Kyoto Daiichi Kagaku Co., Ltd. Method for enzymatically assaying saccharification protein
KR100412259B1 (en) * 2001-09-29 2003-12-31 김창호 preparations of coating composite of internal wall of converter and coating method using it
JP5177399B2 (en) 2007-07-13 2013-04-03 株式会社リコー Surface emitting laser array, optical scanning device, and image forming apparatus
JP5369935B2 (en) 2008-09-05 2013-12-18 株式会社リコー Image forming apparatus

Also Published As

Publication number Publication date
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