JPS6395168A - Spray material for repairing industrial furnace - Google Patents
Spray material for repairing industrial furnaceInfo
- Publication number
- JPS6395168A JPS6395168A JP61242298A JP24229886A JPS6395168A JP S6395168 A JPS6395168 A JP S6395168A JP 61242298 A JP61242298 A JP 61242298A JP 24229886 A JP24229886 A JP 24229886A JP S6395168 A JPS6395168 A JP S6395168A
- Authority
- JP
- Japan
- Prior art keywords
- zircon
- magnesia
- present
- refractory raw
- spraying
- 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 36
- 239000007921 spray Substances 0.000 title description 12
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 40
- 229910052845 zircon Inorganic materials 0.000 claims description 25
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 23
- 239000002994 raw material Substances 0.000 claims description 22
- 239000000395 magnesium oxide Substances 0.000 claims description 20
- 238000005507 spraying Methods 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000004576 sand Substances 0.000 claims description 9
- 235000013312 flour Nutrition 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- 239000000835 fiber Substances 0.000 description 13
- 238000005260 corrosion Methods 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 230000008439 repair process Effects 0.000 description 8
- 239000002893 slag Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 6
- 230000003628 erosive effect Effects 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 239000011449 brick Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000013003 hot bending Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000011819 refractory material Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 238000009849 vacuum degassing Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 229920000914 Metallic fiber Polymers 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910052784 alkaline earth metal Chemical class 0.000 description 1
- 229910000316 alkaline earth metal phosphate Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical class O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 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
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 235000019425 dextrin Nutrition 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
- 238000010304 firing Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Ceramic Products (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) [Abstract] 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)
本発明は工業窯炉の損耗部の補修に用いる吹付材に関す
る。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a spray material used for repairing worn parts of industrial kilns.
(従来技術)
製鉄産業で使用されるRH−DH真空脱ガス炉、溶銑・
溶鋼取鍋、電気炉、転炉などの工業窯炉においては耐火
物による内張りまたは被覆部分が溶鉄やスラグの接触作
用によって損耗されるが、その損傷の進行は一様でない
。そこで、損耗の著しい箇所を主体に吹付補修し、炉寿
命の延長が図られているのが通常である。(Prior art) RH-DH vacuum degassing furnace used in the steel industry, hot metal
In industrial furnaces such as molten steel ladles, electric furnaces, and converters, the refractory linings or coatings are damaged by contact with molten iron and slag, but the progress of this damage is uneven. Therefore, it is common practice to spray repair mainly on the parts that are severely worn out in order to extend the life of the furnace.
ここで、従来の吹付補修に用いられる吹付材について説
明すると、つぎのようである。Here, the spraying materials used in conventional spraying repairs will be explained as follows.
(a)特公昭55−6598号公報に教示されるように
、マグネシア質やマグドロ質などの塩基性材質を基材と
した吹付材。(a) As taught in Japanese Patent Publication No. 55-6598, a spraying material based on a basic material such as magnesia or maguro.
伽)特開昭49−108113号公報や特開昭50−4
9311号公報に教示されるように、アルカリ金属やア
ルカリ土類金属のリン酸塩、ケイ酸塩あるいはカルシウ
ム塩などを結合剤の補助剤として添加した吹付材。佽) JP-A-49-108113 and JP-A-50-4
As taught in Japanese Patent No. 9311, a spray material to which phosphates, silicates or calcium salts of alkali metals or alkaline earth metals are added as binder auxiliaries.
(C1特開昭56−104781号公報や特開昭50−
101409号に教示されるように、リン酸カリウム塩
とリン酸ナトリウム塩あるいはケイ酸塩を結合剤とする
など、主に、結合剤の構成に検討を加えた吹付材。(C1 JP-A-56-104781 and JP-A-50-1989)
As taught in No. 101409, a spray material in which the structure of the binder is mainly studied, such as using a potassium phosphate salt, a sodium phosphate salt, or a silicate as a binder.
発明が解決しようとする問題点)
しかしながら、上述の従来技術(a)〜(C)による吹
付材はいずれも付着後にスラグによる化学的損耗もしく
は溶鉄・スラグによる摩耗あるいは付着界面からの経時
的剥離等のいずれかに問題があり、したがって、耐用性
が充分であるとはいえなかった。Problems to be Solved by the Invention) However, the sprayed materials according to the above-mentioned conventional techniques (a) to (C) all suffer from chemical wear and tear due to slag, abrasion due to molten iron and slag, or peeling over time from the adhesion interface after adhesion. Therefore, it could not be said that the durability was sufficient.
本発明は従来の吹付材における上記欠点を解決すべく成
されたものであって、マグネシア質耐火原料に対してジ
ルコンサンドもしくはジルコンフラワーあるいはこれら
の混合物を所定割合で配合することにより、吹付材に残
存膨張性が付与され、塩基性吹付材がもつ性状を活かし
つつ、その欠点である剥離を防止しようというものであ
る。The present invention has been made to solve the above-mentioned drawbacks of conventional sprayed materials, and by blending zircon sand, zircon flour, or a mixture thereof in a predetermined ratio to magnesia refractory raw materials, the present invention can be made into sprayed materials. It is intended to provide residual expansion properties and to take advantage of the properties of basic spray materials while preventing their drawback, ie, peeling.
(問題点を解決するための手段) 以下、本発明の構成について説明する。(Means for solving problems) The configuration of the present invention will be explained below.
すなわち、本発明の構成要旨とするところは、ジルコン
サンドもしくはジルコンフラワーあるいはその混合物が
5〜50−t%、残部がマグネシア質耐火原料で構成さ
れた耐火原料配合物と適量の結合剤とを含むことを特徴
とする工業窯炉補修用吹付材、にある。That is, the gist of the present invention is that the refractory raw material mixture contains 5 to 50-t% of zircon sand, zircon flour, or a mixture thereof, and the remainder is a magnesia refractory raw material, and an appropriate amount of a binder. A spraying material for repairing industrial kilns, characterized by the following.
ここで、ジルコンサンドは周知のとおり、オーストラリ
ア、アメリカ、インドなどで採掘ささる耐火原料であり
、粒度が主に50〜300μmのものである。一方、ジ
ルコンフラワーはジルコンサンドを粉砕して微粒にした
もので、その粒度は使用目的に応じて適宜、調整される
ため特定化できないが、たとえば、200メツ、シュ以
下、325メツシユ以下などが一般的である。そして、
このジルコンサンドもしくはジルコンフラワーあるいは
その混合物の配合割合はマグネシア耐火原料に対して5
〜50w t%であり、このように限定した理由は5w
t%未満では剥離防止効果に劣り、50w t%を超え
ると、耐溶損性が低下。特に、好ましくは8〜35−t
%である。As is well known, zircon sand is a refractory raw material mined in Australia, America, India, etc., and has a particle size of mainly 50 to 300 μm. On the other hand, zircon flour is made by crushing zircon sand into fine particles, and the particle size cannot be specified because it is adjusted appropriately depending on the purpose of use, but it is generally less than 200 mesh, or less than 325 mesh. It is true. and,
The blending ratio of this zircon sand, zircon flour, or a mixture thereof is 5% to the magnesia refractory raw material.
~50wt%, and the reason for this limitation is 5w
If it is less than t%, the peeling prevention effect will be poor, and if it exceeds 50wt%, the erosion resistance will decrease. Particularly preferably 8 to 35-t
%.
一方、マグネシア質耐火原料としては、合成もしくは天
然のマグネシアクリンカ−あるいはこれらのマグネシア
クリンカ−を主成分としたレンガ屑が使用可能である。On the other hand, as the magnesia-based refractory raw material, synthetic or natural magnesia clinker or brick waste containing these magnesia clinkers as a main component can be used.
なお、場合により、マグネシア質耐火原料の一部をドロ
マイトクリンカ−、スピネルクリンカ−1石灰石、その
他の耐火原料でもって置き換えることも可能であるが、
マグネシアクリンカ−の効果を損なわないように、その
割合は極力、少なくすることが望ましい。また、マグネ
シア質耐火原料の粒度は従来の吹付材と同様で、たとえ
ば、7鶴以下、好ましくは5鶴以下とする。さらに、結
合剤としては一般に使用されているのもで差支えないが
、例示すれば、アルカリ金属、アルカリ土類金属のリン
酸塩、珪酸塩、ホウ酸塩、リン酸アルミニウムなどから
選択される一種または二種以上を使用することができる
。これらの結合剤の添加割合は耐火原料の配合物に対し
て外掛は百分率で2〜104%程度が好ましい。In some cases, it is also possible to replace a part of the magnesia refractory raw material with dolomite clinker, spinel clinker-1 limestone, or other refractory raw materials.
It is desirable to reduce the proportion as much as possible so as not to impair the effect of magnesia clinker. The particle size of the magnesia refractory raw material is the same as that of conventional spray materials, for example, 7 cranes or less, preferably 5 cranes or less. Furthermore, as a binder, any commonly used binder may be used; examples thereof include alkali metal, alkaline earth metal phosphates, silicates, borates, aluminum phosphates, etc. Or two or more types can be used. The addition ratio of these binders is preferably about 2 to 104% in percentage based on the refractory raw material mixture.
本発明吹付材にはこの他、可塑剤として、たとえば、ベ
ントナイト、粘土、デキストリン、CMCなどから選択
される一種または二種以上を添加してもよく、結合剤の
硬化促進剤として消石灰、ケイ沸化ソーダ、塩化アルミ
ニウム、塩化カルシウム、硫酸マグネシウム、グイカル
シウムシリケート、クロムスラグ等から選択される一種
または二種以上を添加しても差支えない、その添加割合
は本発明の効果を損なわないよう、前記耐火原料配合物
に対して外掛は百分率で10−t%以下が好ましい。In addition, one or more types selected from bentonite, clay, dextrin, CMC, etc. may be added as a plasticizer to the spraying material of the present invention, and slaked lime, silica, etc. may be added as a hardening accelerator for the binder. One or more selected from sodium chloride, aluminum chloride, calcium chloride, magnesium sulfate, calcium silicate, chromium slag, etc. may be added, and the addition ratio should be adjusted as described above so as not to impair the effects of the present invention. The outer layer is preferably 10-t% or less based on the refractory raw material blend.
ところで、本発明で使用するジルコンサンドもしくはジ
ルコンフラワーは比重4.5〜4.7程度と耐火原料の
中でも特に、大きいことから、吹付材として使用する場
合に噴射ノズル内の流通、ノズルからの噴出などで他の
耐火原料と比重分離しやすいが、原料配合の段階で、あ
らかじめ、ファイバー類を添加しておくことで、比重分
離を防止でき、組織の均一化で本発明の効果はさらに顕
著なものとなる。ちなみに、添加可能なファイバー類と
しては、ガラスファイバー、石綿、マグネシアファイバ
ー、シリカファイバー、アルミナファイバー、シリカ・
アルミナファイバーなどの無機質ファイバー、ステンレ
ス鋼ファイバー、鉄ファイバー、アルミニウムファイバ
ーなどの金属質ファイバー、ビニロンファイバー、ポリ
ニスデルファイバー、真綿、羊毛、糸屑、故紙叩解物な
どの有機質がある。By the way, the zircon sand or zircon flour used in the present invention has a specific gravity of about 4.5 to 4.7, which is particularly large among refractory raw materials. However, by adding fibers in advance at the raw material blending stage, specific gravity separation can be prevented, and the effect of the present invention is even more remarkable due to the homogenization of the structure. Become something. By the way, fibers that can be added include glass fiber, asbestos, magnesia fiber, silica fiber, alumina fiber, and silica fiber.
There are inorganic fibers such as alumina fibers, metallic fibers such as stainless steel fibers, iron fibers, and aluminum fibers, and organic materials such as vinylon fibers, polynisdel fibers, cotton, wool, thread waste, and beaten waste paper.
これらはいずれも比重分離を防止する効果があるが、と
りわけ、使用時の加熱を受けると焼失・分解して不純物
として残留しない有機質が好ましい。これらファイバー
類の添加割合は使用する材質の比重によって差があるの
で、特に限定しないが、有機質を例にとると、3wt%
以下、好ましくは0.01”1wt%である。また、寸
法はたとえば、長さ50日以下、直径1酊以下とする。All of these have the effect of preventing specific gravity separation, but organic substances that are burnt out and decomposed when heated during use and do not remain as impurities are particularly preferred. The proportion of these fibers added differs depending on the specific gravity of the material used, so it is not particularly limited, but if we take organic material as an example, it is 3wt%.
Below, it is preferably 0.01"1 wt%. Also, the dimensions are, for example, a length of 50 days or less and a diameter of 1 inch or less.
また、無機質繊維では添加割合は5wt%以下、好まし
くは0.1〜2wt%である。Further, in the case of inorganic fibers, the addition ratio is 5 wt% or less, preferably 0.1 to 2 wt%.
なお、以上のように構成される本発明吹付材の吹付施工
方法は従来どおり、乾式または湿式のガンを使用し、被
補修面に対して吹きつける。The method for spraying the spraying material of the present invention configured as described above uses a dry or wet gun to spray the material onto the surface to be repaired, as in the conventional method.
(作用)
本発明吹付材は被補修面に付着後、炉内の高温雰囲気、
溶鉄との接触などで加熱を受けると、ジルコンサンドや
ジルコンフラワーの主成分であるジルコン(ZrO□
・SiO□)が高温で単斜型のZnO□と非結晶質のS
in、とに解離し、これによって生じたジルコニア(Z
rO2)の1 、000℃付近での単斜型C正方型転移
にともなう膨張で吹付材に残存膨張性が付与され、焼結
にともなう体積収縮を防止して被補修面からの吹付材の
剥離を防止する。(Function) After the spraying material of the present invention adheres to the surface to be repaired,
When heated by contact with molten iron, zircon (ZrO□
・SiO□) becomes monoclinic ZnO□ and amorphous S at high temperature.
in, and the resulting zirconia (Z
rO2) No. 1, the expansion associated with the monoclinic C-square transition at around 1,000°C imparts residual expandability to the sprayed material, preventing volumetric shrinkage due to sintering and allowing the sprayed material to peel off from the surface to be repaired. prevent.
また、マグネシア質耐火原料の成分であるMgOはジル
コン成分のZr0z ・Sin、のうち、SiO□と
結合しやすい性質をもつことから、本発明ではマグネシ
ア質耐火原料との組み合わせがジルコンの解離をさらに
促進させることになる。Furthermore, since MgO, which is a component of the magnesia refractory raw material, has the property of easily bonding with SiO□ among the zircon components Zr0z and Sin, in the present invention, the combination with the magnesia refractory raw material further reduces the dissociation of zircon. It will promote this.
(実施例) つぎに、本発明の実施例を比較例とともに説明する。(Example) Next, examples of the present invention will be described together with comparative examples.
第1表に挙げた主原料を用い、第2表に示すような配合
組成の吹付材(本発明実施例!lhl〜13、比較例1
〜4)を調整して■付着性■熱間強度(熱間曲げ強度)
■容積安定性(線変化率)■耐食性(溶損寸法)■耐剥
離性(剥離するまでの回数)■耐用性(耐用回数)の各
試験項目について調べた。なお、このうち、比較例1な
らびに比較例2はジルコン質耐火骨材の割合が本発明範
囲外のものを示し、また、比較例3はジルコン質耐火材
を含まない従来タイプの塩基性吹付材を示し、比較例4
はジルコンと珪石を主材とした非塩基性材料を示す。本
発明で使用する配合原料のうち、主原料の化学分析値は
第1表のとおりである(単位は−t%である)第 1
、表
試験方法、
※l)付着性:1,000℃に加熱したマグネシアクロ
ム質煉瓦に乾式ガンを用いて吹付けし、この時の付着率
wt%で示した。Using the main raw materials listed in Table 1, the spraying material has the composition shown in Table 2 (Examples of the present invention!lhl~13, Comparative Example 1)
~Adhesion ■Hot strength (hot bending strength) by adjusting ~4)
The following test items were investigated: ■ Volume stability (linear change rate) ■ Corrosion resistance (erosion dimensions) ■ Peeling resistance (number of times until peeling) ■ Durability (number of times it can be used). Of these, Comparative Example 1 and Comparative Example 2 have a ratio of zircon refractory aggregate that is outside the range of the present invention, and Comparative Example 3 is a conventional type basic sprayed material that does not contain zircon refractory material. Comparative example 4
indicates a non-basic material mainly composed of zircon and silica. Among the blended raw materials used in the present invention, the chemical analysis values of the main raw materials are as shown in Table 1 (the unit is -t%).
, Table of Test Methods, *l) Adhesion: Sprayed onto magnesia chromium bricks heated to 1,000°C using a dry gun, and expressed as adhesion rate wt%.
※2)熱間曲げ強さ: 40x40x160 m墓の形
状に鋳込み成形し、1 、400℃における曲げ強さを
測定した。*2) Hot bending strength: It was cast into the shape of a 40x40x160m grave, and the bending strength at 1.400°C was measured.
※3)線変化率:40X40X160龍の形状に鋳込み
成形し、1 、400℃で3時間加熱し、JISR26
54に準じて線変化率を算出した。*3) Linear change rate: Cast into a 40x40x160 dragon shape, heat at 400℃ for 3 hours, and pass JISR26.
The linear change rate was calculated according to 54.
※4)耐食性:試験片を鋳込み成形し、重量比で転炉ス
ラグ:鋼片=4:lを侵食剤として回転侵食試験を行っ
た。溶損寸法が小さい程耐食性に優れる。*4) Corrosion resistance: A test piece was cast and subjected to a rotary erosion test using a weight ratio of converter slag:steel slab = 4:l as the corrosive agent. The smaller the erosion dimension, the better the corrosion resistance.
※5)耐剥離性:l、000℃に加熱したマグネシアク
ロム質レンガに乾式ガンを用いて吹付を行い、これを電
気炉内に装入し、加熱・冷却を繰り返して剥離が認めら
れるまでの繰り返し回数を調べた。加熱冷却の条件は1
、500℃で30分加熱した後、800℃まで冷却し
、これを繰り返す。*5) Peeling resistance: Spraying is performed using a dry gun on magnesia chromium bricks heated to 1,000°C, placed in an electric furnace, and heated and cooled repeatedly until peeling is observed. Checked the number of repetitions. The conditions for heating and cooling are 1.
, after heating at 500°C for 30 minutes, cooling to 800°C, and repeating this process.
※6)実炉テスト:内外周がアルミナ質キャスタブル耐
火物、内周がマグネシアクロム質レンガで構成されるR
H真空脱ガス炉の浸漬管を乾式吹付ガンを用いて吹付補
修し、吹付材の耐用回数を調べた。なお、吹付補修開始
時の浸漬管外表面の温度は約1 、000℃である。ま
た、吹付材の耐用状況は目視観察による評価である。*6) Actual furnace test: R consisting of alumina castable refractories on the inner and outer peripheries and magnesia chromium bricks on the inner periphery.
The immersion pipe of the H vacuum degassing furnace was repaired by spraying using a dry spray gun, and the service life of the sprayed material was investigated. Note that the temperature of the outer surface of the immersion tube at the start of spray repair is approximately 1,000°C. In addition, the durability of the sprayed material is evaluated by visual observation.
以上のように、本発明にかかる実験例ならびに比較例の
結果について考察するに、従来の塩基性吹付材(比較例
3)は耐剥離性に劣り、また、ジルコン−珪石質吹付補
修材(比較例4)は耐食性に劣っている。これに対し、
本発明実施例の吹付材によれば、塩基性吹付材のもつ耐
食性を低下することなく、その欠点である焼結収縮に起
因する剥離を解消できる。その結果、実炉試験において
従来品の1.5〜3倍程度の耐用性が得られた。また、
耐食性テストに関し、回転侵食試験によれば、従来のマ
グネシア質吹付材に比べて本発明品はスラグ浸透深さが
大幅に浅くなり、これが耐食性向上の一因であると考え
られる。これはジルコンの解離で生じたSiO2がガラ
ス化し、スラグの浸透を防止するためと思われる。一般
にジルコン質耐火原料は塩基性スラグに対して耐食性に
劣ることが知られているが、本発明ではマグネシア質耐
火原料と組み合わせること、添加量を特定の範囲に限定
することなどで耐食性の低下もない。As described above, considering the results of the experimental examples and comparative examples according to the present invention, the conventional basic spraying material (Comparative Example 3) is inferior in peeling resistance, and the zircon-silica spraying repair material (comparative example 3) is inferior in peeling resistance. Example 4) has poor corrosion resistance. On the other hand,
According to the sprayed material of the embodiment of the present invention, it is possible to eliminate the peeling caused by sintering shrinkage, which is a drawback of the basic sprayed material, without reducing the corrosion resistance of the basic sprayed material. As a result, in actual furnace tests, durability was approximately 1.5 to 3 times that of conventional products. Also,
Regarding the corrosion resistance test, according to the rotary erosion test, the slag penetration depth of the product of the present invention was significantly shallower than that of conventional magnesia-based sprayed materials, and this is thought to be one of the reasons for the improvement in corrosion resistance. This is thought to be because SiO2 generated by dissociation of zircon becomes vitrified and prevents slag penetration. It is generally known that zircon refractory raw materials are inferior in corrosion resistance to basic slag, but in the present invention, by combining them with magnesia refractory raw materials and by limiting the amount added to a specific range, the corrosion resistance can be reduced. do not have.
(発明の効果)
以上のように構成される本発明吹付材を工業窯炉の損耗
部の補修に対して適用すれば、付着性がよく、付着後の
耐用性もきわめて優れており、かつ剥離の発生もないこ
とから、操炉の安定化、吹付材原単位・補修工数の低減
による補修費の減少、補修回数の低減による炉稼動効率
の向上などの効果が得られる。−(Effects of the Invention) When the spray material of the present invention configured as described above is applied to the repair of damaged parts of industrial kilns, it has good adhesion, extremely excellent durability after adhesion, and is easy to peel off. Since there is no occurrence of any damage, effects such as stabilization of furnace operation, reduction in repair costs due to reduction in spray material consumption and repair man-hours, and improvement in furnace operating efficiency due to reduction in the number of repairs can be achieved. −
第1図はマグネシア−ジルコン質吹付材において、ジル
コンサンドの配合量と1 、400℃の温度で3時間焼
成した後の線変化率の関係を示すグラフ、第2図はマグ
ネシア−ジルコン質吹付材において、ジルコンサンドの
配合量と耐食性の関係を示すグラフである。
・、′A−4・
:、;−IR・−2
・−−ノ′Figure 1 is a graph showing the relationship between the blended amount of zircon sand and the linear change rate after firing at a temperature of 1,400°C for 3 hours in magnesia-zircon sprayed material, and Figure 2 is a graph showing the relationship between magnesia-zircon sprayed material 2 is a graph showing the relationship between the amount of zircon sand and corrosion resistance.・,'A-4・ :,;-IR・-2 ・--ノ'
Claims (1)
の混合物が5〜50wt%、残部がマグネシア質耐火原
料で構成された耐火原料配合物と適量の結合剤とを含む
ことを特徴とする工業窯炉補修用吹付材。A spraying material for repairing an industrial kiln, comprising a refractory raw material composition consisting of 5 to 50 wt% of zircon sand, zircon flour, or a mixture thereof, and the remainder being a magnesia refractory raw material, and an appropriate amount of a binder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61242298A JPS6395168A (en) | 1986-10-13 | 1986-10-13 | Spray material for repairing industrial furnace |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61242298A JPS6395168A (en) | 1986-10-13 | 1986-10-13 | Spray material for repairing industrial furnace |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6395168A true JPS6395168A (en) | 1988-04-26 |
JPH0531517B2 JPH0531517B2 (en) | 1993-05-12 |
Family
ID=17087151
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61242298A Granted JPS6395168A (en) | 1986-10-13 | 1986-10-13 | Spray material for repairing industrial furnace |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6395168A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0393674A (en) * | 1989-09-06 | 1991-04-18 | Harima Ceramic Co Ltd | Basic casting execution refractory |
-
1986
- 1986-10-13 JP JP61242298A patent/JPS6395168A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0393674A (en) * | 1989-09-06 | 1991-04-18 | Harima Ceramic Co Ltd | Basic casting execution refractory |
Also Published As
Publication number | Publication date |
---|---|
JPH0531517B2 (en) | 1993-05-12 |
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