JPS63156078A - Spray mending material for metal refining furnace - Google Patents
Spray mending material for metal refining furnaceInfo
- Publication number
- JPS63156078A JPS63156078A JP61301943A JP30194386A JPS63156078A JP S63156078 A JPS63156078 A JP S63156078A JP 61301943 A JP61301943 A JP 61301943A JP 30194386 A JP30194386 A JP 30194386A JP S63156078 A JPS63156078 A JP S63156078A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- raw material
- repair
- magnesia
- 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 description 33
- 239000007921 spray Substances 0.000 title claims description 9
- 229910052751 metal Inorganic materials 0.000 title claims description 7
- 239000002184 metal Substances 0.000 title claims description 7
- 238000007670 refining Methods 0.000 title 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 28
- 239000002994 raw material Substances 0.000 claims description 27
- 230000008439 repair process Effects 0.000 claims description 23
- 239000010459 dolomite Substances 0.000 claims description 14
- 229910000514 dolomite Inorganic materials 0.000 claims description 14
- 239000000395 magnesium oxide Substances 0.000 claims description 14
- 239000001488 sodium phosphate Substances 0.000 claims description 7
- 229910000162 sodium phosphate Inorganic materials 0.000 claims description 7
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 7
- 238000003723 Smelting Methods 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 5
- 239000011574 phosphorus Substances 0.000 claims description 5
- 239000007785 strong electrolyte Substances 0.000 claims description 5
- 239000001506 calcium phosphate Substances 0.000 claims description 3
- 229910000389 calcium phosphate Inorganic materials 0.000 claims description 3
- 235000011010 calcium phosphates Nutrition 0.000 claims description 3
- 159000000011 group IA salts Chemical class 0.000 claims description 3
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 claims description 3
- 230000007797 corrosion Effects 0.000 description 8
- 238000005260 corrosion Methods 0.000 description 8
- 239000002893 slag Substances 0.000 description 8
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 7
- 239000000292 calcium oxide Substances 0.000 description 7
- 235000012255 calcium oxide Nutrition 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 238000010276 construction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 239000011449 brick Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000011465 paving brick Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- ATRMIFNAYHCLJR-UHFFFAOYSA-N [O].CCC Chemical compound [O].CCC ATRMIFNAYHCLJR-UHFFFAOYSA-N 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 235000019700 dicalcium phosphate Nutrition 0.000 description 2
- 229940095079 dicalcium phosphate anhydrous Drugs 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000011822 basic refractory Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- JUNWLZAGQLJVLR-UHFFFAOYSA-J calcium diphosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O JUNWLZAGQLJVLR-UHFFFAOYSA-J 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 229940043256 calcium pyrophosphate Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 235000019821 dicalcium diphosphate Nutrition 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 238000004901 spalling Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
Landscapes
- Ceramic Products (AREA)
- Furnace Housings, Linings, Walls, And Ceilings (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 産業上の利用分野 不発明は、金属精錬炉用吹付補修材に関する。[Detailed description of the invention] Industrial applications The invention relates to a spray repair material for metal smelting furnaces.
従来の技術とその問題点
近年転炉等の金属精錬炉において、内張り材として耐用
性に優れたマグネシア−炭素質煉瓦が使用されるように
なるとともに、スラグライン部等の局部溶損の補修が炉
寿命を大きく左右するようになってきた。従来局部溶4
箇所を補修するに当っては、主に吹付補修法が採用され
ている。これは、耐火原料と結合剤とからなる混合物(
吹付材)を吹付ノズルの先で水と混合し、炉壁に吹付け
て補修層を形成させる方法である。従来吹付材としては
、吹付時の施工性、特に炉壁への付着性を重視して、マ
グネシア質、ドロマイト質、マグネシアート[コマイト
〈以下マグドロという)質等の塩基性耐火原料、リンW
!i塩等の結合剤及びマグネシア超微粉、ライム化合物
等のリン酸塩の硬化剤を含む高粘性且つ早硬化性の5の
が主に使用されてきた。ところが、1)これらの補修材
では、その耐用性及び熱間強度が不充分であること、2
)最近の操業条件の変更によって、トラニオン部等の急
傾斜箇所の溶損がなくなり、スラグライン等の緩傾斜部
分のみが溶損するようになったこと等の理由により、低
粘性且つ遅硬化性の補修材が望まれるようになってきた
。これは、低粘性且つ遅硬化性の補修材は、熱間での施
工時に材料が沸騰するため、充填と乾燥とが同時に進行
し、施工体がm密となり、施工体の耐用性及び強度が向
上するという利点を有しているからである。従って、遅
硬化性の補修材を得るために、従来の補修材の成分中リ
ン酸塩の硬化剤を添加しないもの等が使用されているが
、以下の如き欠点があり好ましくない。即ち、ドロマイ
ト質、マグドロ質等のドロマイト含有原料を使用すると
、材料の沸騰期間中にドロマイト原料から溶出するカル
シアと結合剤であるリン酸ナトリウムとが反応して水に
不溶な高分子リン酸塩が生成し、硬化が早くなるという
問題点が生じる。一方マグネシア原料は、リン酸ナトリ
ウムとの反応性に乏しいが、耐用性、特に熱間での体積
安定性に欠け、またスラグ浸透が大きいので構造スポー
リングの発生が著るしい等の材質としてマグドロ材質よ
りも劣る欠点を有している。Conventional technology and its problems In recent years, highly durable magnesia-carbon bricks have come to be used as lining materials in metal smelting furnaces such as converters, and repair of local melting damage such as in slag lines has become more and more important. It has come to have a great influence on the life of the furnace. Conventional local dissolution 4
When repairing areas, spraying repair methods are mainly used. This is a mixture (
This is a method in which spraying material) is mixed with water at the tip of a spray nozzle and sprayed onto the furnace wall to form a repair layer. Conventional spraying materials include basic refractory raw materials such as magnesia, dolomite, and magnesiat (comite (hereinafter referred to as "Magdro")), phosphorus W, etc., with emphasis on workability during spraying, especially adhesion to furnace walls.
! A highly viscous and fast-curing material containing a binder such as i-salt and a phosphate curing agent such as ultrafine magnesia powder or a lime compound has been mainly used. However, 1) these repair materials have insufficient durability and hot strength;
) Due to recent changes in operating conditions, the erosion of steeply sloped parts such as trunnions has disappeared, and only gently sloped parts such as slag lines are now melted. Repair materials are now in demand. This is because low-viscosity and slow-curing repair materials boil when applied hot, so filling and drying proceed simultaneously, making the construction body dense and reducing its durability and strength. This is because it has the advantage of improving performance. Therefore, in order to obtain a slow-curing repair material, conventional repair materials that do not contain a phosphate curing agent are used, but these are undesirable due to the following drawbacks. That is, when a dolomite-containing raw material such as dolomite or magdromite is used, calcia eluted from the dolomite raw material during the boiling period of the material reacts with sodium phosphate, which is a binder, to form a water-insoluble polymeric phosphate. This causes the problem that the hardening process becomes faster. On the other hand, magnesia raw materials have poor reactivity with sodium phosphate, but they also lack durability, especially volumetric stability under hot conditions, and are prone to structural spalling due to large slag penetration. It has disadvantages that are inferior to the material.
問題点を解決するための手段
本発明者は、上記従来技術の問題点に鑑みて鋭意研究を
重ねた結果、マグドロ原料を耐火骨材として使用しても
、縮合リン酸とリンを含有しない強電解質のアルカリ塩
とを併用し、且つアルカリを含有することによる吹付材
の熱間強度の低下を防止するために難水溶性のリン酸カ
ルシウムを添加することによって、遅硬化性であり、耐
食性等の耐用性に茗るしくゆれ、炉壁との接着強電が高
い金属精錬炉用吹付補修材が得られることを見い出し、
本発明を完成した。Means for Solving the Problems In view of the above-mentioned problems of the prior art, the inventor of the present invention has conducted extensive research and found that even if Magdro raw material is used as a refractory aggregate, a strong material that does not contain condensed phosphoric acid and phosphorus. By using an electrolyte with an alkali salt and adding calcium phosphate, which is poorly water-soluble, to prevent the hot strength of the sprayed material from decreasing due to the alkali content, it has slow curing properties and has long-lasting properties such as corrosion resistance. We discovered that it is possible to obtain a spray repair material for metal smelting furnaces that exhibits strong elasticity and strong adhesion to the furnace wall.
The invention has been completed.
即ち本発明は、ドロマイト原料30〜70単口%とマグ
ネシア原料70〜30重1%とから成る耐火原料100
重凸単1縮合リン酸ナトリウム2.5〜7.0千G部、
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「シム0.3〜1.5重量部を含有する金
属精錬炉用吹付補修材に係る。That is, the present invention provides a refractory raw material 100 consisting of 30 to 70% by weight of dolomite raw material and 70 to 30% by weight of magnesia raw material.
2.5 to 7.0 thousand G parts of heavy convex single condensed sodium phosphate,
The present invention relates to a spray repair material for metal smelting furnaces containing 0.2 to 1.5 parts by weight of a strong electrolyte alkali salt and 0.3 to 1.5 parts by weight of poorly soluble calci phosphate shim.
本発明では、耐火原料としてドロマイト原料及びマグネ
シア原料を使用する。In the present invention, dolomite raw materials and magnesia raw materials are used as refractory raw materials.
ドロマイト原料としては、この分野で常用されるのもの
が何れも使用できるが、通常カルシア含に40%以上、
嵩比重3.20以上のものを使用する。但し、材料の体
積安定性、スラグ浸透防止性等を考慮すると、特にカル
シア含量が55%以上のものが好ましい。ドロマイト原
料の配合けは、耐火原料全量の30〜70重ω%程度と
するのがよい。30重M%未満では、カルシアの効果が
ほとんど発揮されず、一方70重0%を越えると、ダス
ティングのために、ドロマイト微粉が使用できない関係
上、粒度構成で制約を受け、吹付作業性、耐食性等が低
下する。As the dolomite raw material, any material commonly used in this field can be used, but it usually contains 40% or more of calcia,
Use one with a bulk specific gravity of 3.20 or more. However, in consideration of the volume stability of the material, the ability to prevent slag penetration, etc., it is particularly preferable that the calcia content be 55% or more. The content of the dolomite raw material is preferably about 30 to 70% by weight of the total amount of the refractory raw material. If it is less than 30% by weight, the effect of calcia is hardly exhibited, while if it exceeds 70% by weight, dolomite fine powder cannot be used due to dusting, and the particle size structure is restricted, resulting in poor spray workability. Corrosion resistance etc. decrease.
マグネシア原料としては、海水マグネシア、電融マグネ
シア、天然マグネシア等この分野で常用されるものが使
用できるが、通常マグネシア含量92%、SiO2含は
5%以下、
CaO/S i 02 =0.3以上のものを使用ザる
。As the magnesia raw material, those commonly used in this field such as seawater magnesia, electrofused magnesia, and natural magnesia can be used, but the magnesia content is usually 92%, the SiO2 content is 5% or less, and CaO/S i 02 = 0.3 or more. I'll use that one.
耐火原料の粒径は特に限定されず、適宜選択すればよい
が、通常粒径5〜1M程度の粗粒を30〜50重程度、
粒径1aI以下の中間粒を20〜40重程度及び0.0
74m以下の微粉を20〜40重程度含むようにして使
用すればよい。但し、材料のダスティングを考慮すると
、粒径0.074 重量以下のドロマイト微粉を使用し
ないほうが望ましい。The particle size of the refractory raw material is not particularly limited and may be selected as appropriate, but usually coarse particles with a particle size of about 5 to 1M are used, about 30 to 50 kg,
Intermediate particles with a particle size of 1aI or less are about 20 to 40 weight and 0.0
It may be used so that it contains about 20 to 40 weight of fine powder of 74 m or less. However, in consideration of material dusting, it is preferable not to use dolomite fine powder with a particle size of 0.074 weight or less.
本発明では、縮合リン酸ナトリウムとリンを含有しない
強電解質のアルカリ塩とを併用することによって、補修
材の硬化を遅延させる。これは、塩析現染、即ち2種の
強電解質塩の水への溶解磨が互いの濃度によって影響さ
れ、通常単独の場合より低下するという現雫を利用した
ものであり、これによって、硬化反応即ち水溶性のリン
酸ナトリウムのNaイオンと材料中のCaイオンとが置
換して、水に不溶な高分子リン酸塩が生成するという反
応が遅延されるのである。In the present invention, curing of the repair material is delayed by using condensed sodium phosphate and an alkaline salt of a strong electrolyte that does not contain phosphorus. This method takes advantage of salting-out dyeing, in which the dissolution of two strong electrolyte salts in water is affected by the concentration of each other, and is usually lower than when they are used alone. The reaction, that is, the Na ions of the water-soluble sodium phosphate are replaced with the Ca ions in the material to form a water-insoluble polymer phosphate, is delayed.
縮合リン酸ナトリウムとしては、通常のものが何れも使
用でき、例えば、ビロリン酸ナトリウム、トリポリリン
酸ナトリウム、テトラポリリン酸ナトリウム、ヘキサメ
タリン酸ナトリウム等を挙げることができる。その配合
量は、耐火原料100重量部に対し2.5〜7.0重量
部程度とするのがよい。2.5重置部未満では、使用初
期に充分な接着強度が発現されず、一方7.0重の部を
越えると、材料中のフラックス苗が増加して耐食性が低
下する。Any conventional condensed sodium phosphate can be used, and examples thereof include sodium birophosphate, sodium tripolyphosphate, sodium tetrapolyphosphate, and sodium hexametaphosphate. The blending amount is preferably about 2.5 to 7.0 parts by weight per 100 parts by weight of the refractory raw material. If the overlap is less than 2.5 parts, sufficient adhesive strength will not be developed in the initial stage of use, while if it exceeds 7.0 parts, flux seedlings in the material will increase and corrosion resistance will decrease.
リンを含有しない強電解質のアルカリ塩としては、溶解
度が10以上の弱酸性から弱塩基性のナトリウム塩若し
くはカリウム塩が何れも使用でき、例えば、Nac:、
91KC(1等の塩化物、Na2CO3、K2 CO3
等の炭酸塩、CH3COONa等の酢酸塩等を挙げるこ
とかできる。その配合量、耐火原料100重量に対し0
.2〜1.5重量部程度とするのがよい。As the alkaline salt of a strong electrolyte that does not contain phosphorus, any weakly acidic to weakly basic sodium salt or potassium salt having a solubility of 10 or more can be used, such as Nac:,
91KC (1st grade chloride, Na2CO3, K2 CO3
and acetates such as CH3COONa. Its blending amount is 0 per 100 weight of refractory raw materials.
.. The amount is preferably about 2 to 1.5 parts by weight.
0.2重石部未満では、硬化遅延効果が乏しく、一方1
.5重量部を越えると、リン酸塩の溶解量が減少し、乾
燥後の強度が発現しにくくなるとともに、CQ1CO2
等の加熱中に分解する成分を有するため、昇熱中に爆裂
する、耐食性が低下する等の問題点が生ずる。If the amount is less than 0.2 parts, the curing retardation effect is poor;
.. If it exceeds 5 parts by weight, the amount of dissolved phosphate will decrease, making it difficult to develop strength after drying, and CQ1CO2
Since it contains components that decompose during heating, problems such as explosion during heating and a decrease in corrosion resistance occur.
難水溶性リン酸カルシウムとしては、通常のものが何れ
も使用でき、例えば、第2リン酸カルシウム、第3リン
酸カルシCクム、ピロリン酸カルシウム等を挙げること
ができる。その配合mは、耐火原料100千m部に対し
0.3〜1.5重訂部程度とするのがよい。0.3重B
部未満では、熱間強度向上効果が少く、一方1.5重訂
部を越えても効果が余り変らず不経済である。As the poorly water-soluble calcium phosphate, any of the usual ones can be used, such as dibasic calcium phosphate, dibasic calcium phosphate, calcium pyrophosphate, and the like. The mixing ratio m is preferably about 0.3 to 1.5 parts per 100,000 m parts of the refractory raw material. 0.3 layer B
If it is less than 1.5 parts, the effect of improving hot strength will be small, while if it exceeds 1.5 parts, the effect will not change much and it will be uneconomical.
本発明補修材は、上記各原料の所定凸を、常法に従い、
例えば、アイリッヒミキサー等で混合することによって
製造される。The repair material of the present invention is prepared by adding a predetermined convexity of each of the above raw materials according to a conventional method.
For example, it is manufactured by mixing with an Eirich mixer or the like.
本発明補修材を用いて溶損個所の補修を行なうに当って
は、この分野で行なわれている吹付補修方法が何れも採
用できる。When repairing a damaged area using the repair material of the present invention, any spray repair method used in this field can be employed.
発明の効果
本発明金属精錬炉用吹付補修材は、極めて優れた耐食性
及び炉壁への接着強度を有し、著るしく高い耐用性を示
す。Effects of the Invention The spray repair material for metal smelting furnaces of the present invention has extremely excellent corrosion resistance and adhesive strength to the furnace wall, and exhibits extremely high durability.
実 施 例
以下に実施例及び比較例を挙げ、本発明をより一層明瞭
なものとする。EXAMPLES Examples and comparative examples are given below to make the present invention even clearer.
実施例1〜5及び比較例1.2
耐火原料100fiei1部に対し、第1表に示す配合
割合(重量部)で各原料を加え、アイリッヒミキサーで
混合し、本発明補修材及び従来の補修材を製造した。尚
ドロマイト原料としては、カルシア含量58%、嵩比重
3.25の天然ドロマイトを、マグネシア原料としては
、マグネシア含量94%、3i02含量2.5%、
CaO/S i 02 =0.4の海水マグネシアを、
また縮合リン酸としては、Na2O含ff123%、P
2O5含岳63%のテトラポリリン酸ナトリウムを用い
た。Examples 1 to 5 and Comparative Example 1.2 To 1 part of 100 fiei of refractory raw materials, each raw material was added in the proportions (parts by weight) shown in Table 1, mixed with an Eirich mixer, and the repair material of the present invention and the conventional repair material were mixed. manufactured the material. The dolomite raw material is natural dolomite with a calcia content of 58% and a bulk specific gravity of 3.25, and the magnesia raw material is seawater magnesia with a magnesia content of 94%, a 3i02 content of 2.5%, and CaO/S i 02 = 0.4. of,
In addition, as condensed phosphoric acid, Na2O content 123%, P
Sodium tetrapolyphosphate containing 63% 2O5 was used.
得られた補修材を水と混練した後、酸素−プロパン炉中
で、1200℃に加熱されている煉瓦枠に流し込み、そ
の硬化性状を判定するとともに、後記品質試験に供する
施工体試料を作製した。試料の寸法は、170x300
x60mであり、170X300#lj+の面が煉瓦枠
の敷煉瓦(ドロマイト質、250x350x110Im
)に接着するようにした。敷線瓦表面には、予めスラグ
コーティングを施し、施工体く補修層)と敷煉瓦とがス
ラブ面を介して接着されるようにした。¥、tられた施
工体試料について、緻密性及び耐食性を調べた。After kneading the obtained repair material with water, it was poured into a brick frame heated to 1200°C in an oxygen-propane furnace, and its hardening properties were determined, and a construction sample was prepared for the quality test described later. . The dimensions of the sample are 170x300
x60m, 170x300#lj+ side is brick frame paving brick (dolomite, 250x350x110Im
). A slag coating was applied to the surface of the paving line tile in advance, so that the construction work (repair layer) and the paving brick were bonded through the slab surface. The compactness and corrosion resistance of the constructed samples were examined.
緻密性試験としては、J l5R−2205に1llt
1.;、気孔率と嵩比重を測定した。耐食性試験として
は、施工体試料から、外寸法径50mX高さ50重量、
凹部寸法径20#llI×高さ20Jl#Iのルツボ型
試料を切り出し、この試料に30gの転炉スラグを充填
し、次いでこれを酸素−プロパン炉において1700℃
で3時間焼成した後、該ルツボ型試料を縦方向に切断し
、スラグによる溶損面積及びスラグの浸透面積を測定し
た。接着強度は、敷き煉瓦と施工体とからなる寸法40
X40X120履の試料を切り出し、JISR−221
3に準じて接着界面を中心として常温曲げ強度試験を行
なって測定した。結果を第1表に示す。For the compactness test, 1llt was used for J15R-2205.
1. , porosity and bulk specific gravity were measured. For the corrosion resistance test, from the construction sample, the outer dimensions were 50 m in diameter x 50 m in height,
A crucible-shaped sample with a concave diameter of 20#llI x height of 20Jl#I was cut out, this sample was filled with 30g of converter slag, and then heated at 1700°C in an oxygen-propane furnace.
After firing for 3 hours, the crucible-shaped sample was cut in the longitudinal direction, and the area eroded by the slag and the area permeated by the slag were measured. The adhesive strength is 40mm, which is the size of the paving brick and the construction body.
Cut out a sample of X40X120 shoes, JISR-221
3, a room temperature bending strength test was conducted centering around the adhesive interface to measure the strength. The results are shown in Table 1.
第1表から、本発明補修材が従来の補修材に比べ、硬化
時間が良く、緻密性に優れ、耐食性、接着強度等に優れ
ていることが判る。From Table 1, it can be seen that the repair material of the present invention has a faster curing time, better density, corrosion resistance, adhesive strength, etc. than conventional repair materials.
(以 上)(that's all)
Claims (1)
70〜30重量%とから成る耐火原料100重量部、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。1. 100 parts by weight of a refractory raw material consisting of 30 to 70% by weight of dolomite raw material and 70 to 30% by weight of magnesia raw material, 2.5 to 7.0 parts by weight of condensed sodium phosphate, and 0.0 parts by weight of a strong electrolyte alkaline salt that does not contain phosphorus. A spray repair material for a metal smelting furnace containing 2 to 1.5 parts by weight and 0.3 to 1.5 parts by weight of hardly soluble calcium phosphate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61301943A JPH0764650B2 (en) | 1986-12-17 | 1986-12-17 | Spray repair material for metal refining furnace |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61301943A JPH0764650B2 (en) | 1986-12-17 | 1986-12-17 | Spray repair material for metal refining furnace |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63156078A true JPS63156078A (en) | 1988-06-29 |
JPH0764650B2 JPH0764650B2 (en) | 1995-07-12 |
Family
ID=17902977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61301943A Expired - Lifetime JPH0764650B2 (en) | 1986-12-17 | 1986-12-17 | Spray repair material for metal refining furnace |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0764650B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009215096A (en) * | 2008-03-07 | 2009-09-24 | Kurosaki Harima Corp | Hot filling material |
JP6408678B1 (en) * | 2017-10-25 | 2018-10-17 | 黒崎播磨株式会社 | Hot dry spray material and hot dry spray construction method |
-
1986
- 1986-12-17 JP JP61301943A patent/JPH0764650B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009215096A (en) * | 2008-03-07 | 2009-09-24 | Kurosaki Harima Corp | Hot filling material |
JP6408678B1 (en) * | 2017-10-25 | 2018-10-17 | 黒崎播磨株式会社 | Hot dry spray material and hot dry spray construction method |
WO2019082740A1 (en) * | 2017-10-25 | 2019-05-02 | 黒崎播磨株式会社 | Hot dry spraying material and method for hot dry spraying work |
Also Published As
Publication number | Publication date |
---|---|
JPH0764650B2 (en) | 1995-07-12 |
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