JPH1171183A - Flame spraying material - Google Patents
Flame spraying materialInfo
- Publication number
- JPH1171183A JPH1171183A JP9230988A JP23098897A JPH1171183A JP H1171183 A JPH1171183 A JP H1171183A JP 9230988 A JP9230988 A JP 9230988A JP 23098897 A JP23098897 A JP 23098897A JP H1171183 A JPH1171183 A JP H1171183A
- Authority
- JP
- Japan
- Prior art keywords
- sintered
- magnesia
- clinker
- slag
- cao
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/62204—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products using waste materials or refuse
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B33/00—Clay-wares
- C04B33/02—Preparing or treating the raw materials individually or as batches
- C04B33/13—Compounding ingredients
- C04B33/132—Waste materials; Refuse; Residues
- C04B33/1324—Recycled material, e.g. tile dust, stone waste, spent refractory material
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/62605—Treating the starting powders individually or as mixtures
- C04B35/62645—Thermal treatment of powders or mixtures thereof other than sintering
- C04B35/62665—Flame, plasma or melting treatment
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/66—Monolithic refractories or refractory mortars, including those whether or not containing clay
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3206—Magnesium oxides or oxide-forming salts thereof
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3208—Calcium oxide or oxide-forming salts thereof, e.g. lime
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3208—Calcium oxide or oxide-forming salts thereof, e.g. lime
- C04B2235/321—Dolomites, i.e. mixed calcium magnesium carbonates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/327—Iron group oxides, their mixed metal oxides, or oxide-forming salts thereof
- C04B2235/3272—Iron oxides or oxide forming salts thereof, e.g. hematite, magnetite
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/60—Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、接着性および耐食
性に優れた塩基性質の火炎溶射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 basic flame sprayed material having excellent adhesiveness and corrosion resistance.
【0002】[0002]
【従来の技術】転炉、溶解炉、AOD炉、取鍋、タンデ
ッシュ、真空脱ガス炉などの工業窯炉の内張り損傷部
を、火炎溶射法をもって補修することが行われている。
この方法は、耐火物微粉末を高速・高温の火炎中に通
し、溶融または半溶融状態にして損傷部分に溶射するも
のである。この火炎溶射法によると、緻密かつ高強度の
補修体組織が形成され、優れた補修効果が得られる。2. Description of the Related Art Damaged linings in industrial kilns such as converters, melting furnaces, AOD furnaces, ladles, tundishes, and vacuum degassing furnaces are repaired by flame spraying.
In this method, a refractory fine powder is passed through a high-speed, high-temperature flame, and is melted or semi-molten to be sprayed on a damaged portion. According to this flame spraying method, a dense and high-strength repair body structure is formed, and an excellent repair effect is obtained.
【0003】従来、この火炎溶射に使用される溶射材と
して、MgO−CaO系の塩基性質が提案されている。
例えば特開昭63−107873号公報には石灰質クリ
ンカー、マグネシアクリンカーおよびスラグを配合した
材質が、特開昭63−107872号公報には特定量の
Fe2 O3 を含有した石灰質クリンカーおよびマグネシ
アクリンカー(必要によりスラグを添加)を配合した材
質が示されている。Hitherto, as a thermal spraying material used for the flame spraying, basic properties of MgO—CaO system have been proposed.
For example, in JP 63-107873 discloses calcareous clinker, magnesia clinker and slag material blended with, calcareous clinker and magnesia clinker in JP 63-107872 containing Fe 2 O 3 of a specific amount ( The material to which slag is added (if necessary) is shown.
【0004】[0004]
【発明が解決しようとする課題】塩基性質の溶射材は火
炎溶射材の中でも耐食性が特に優れており、従来材質の
主流となっている。しかし、その反面、塩基性質原料の
融点が高いことから接着性(被補修面に対する接着強
度)に劣る欠点がある。そこで、従来は低融点物質であ
るスラグの配合によって、接着性の向上を図っている。The thermal sprayed material having a basic property is particularly excellent in corrosion resistance among flame sprayed materials, and has been the mainstream material of the prior art. However, on the other hand, there is a disadvantage that the adhesiveness (adhesive strength to the surface to be repaired) is poor due to the high melting point of the basic material. In view of this, conventionally, an improvement in adhesiveness has been achieved by blending slag, which is a low-melting substance.
【0005】接着性の面でスラグの配合は不可欠であ
る。前記したように、特定量のFe2O3 を含有した石
灰質クリンカーを使用することも提案されているが、ス
ラグと組み合わせて使用しない限り、接着性は十分なも
のではない。しかし、スラグの配合は同時に溶射材の耐
食性の低下を招くことから、十分な接着性を得るだけの
量を添加することはできない。[0005] The slag is indispensable in terms of adhesiveness. As mentioned above, the use of calcareous clinker containing a certain amount of Fe 2 O 3 has been proposed, but the adhesion is not sufficient unless used in combination with slag. However, the addition of slag simultaneously lowers the corrosion resistance of the sprayed material, so that it is not possible to add an amount sufficient to obtain sufficient adhesiveness.
【0006】本発明はこのような実情に鑑み、接着性と
耐食性に優れた塩基性質溶射材を提供することを目的と
して成されたものである。The present invention has been made in view of such circumstances, and has as its object to provide a basic spray material having excellent adhesion and corrosion resistance.
【0007】[0007]
【課題を解決するための手段及び作用】本発明は、化学
成分でCaO:35〜80wt%、MgO:18〜63
wt%、Fe2 O3 :1.8〜7wt%を含み、前記C
aOとMgOの合量が93wt%以上の焼結カルシア−
マグネシアクリンカーを5〜40wt%と、焼結マグネ
シアクリンカーおよび/または電融マグネシアを30〜
70wt%と、スラグ10〜50wt%とを配合した火
炎溶射材である。更に、他の耐火原料を30wt%以下
加えても良い。According to the present invention, a chemical composition of CaO: 35 to 80 wt% and MgO: 18 to 63 are used.
wt%, Fe 2 O 3: includes 1.8~7wt%, the C
Sintered calcia having a total content of aO and MgO of 93% by weight or more
Magnesia clinker is 5 to 40 wt%, and sintered magnesia clinker and / or electrofused magnesia is 30 to 40 wt%.
This is a flame spray material containing 70 wt% and 10 to 50 wt% of slag. Further, another refractory raw material may be added in an amount of 30 wt% or less.
【0008】本発明によれば、従来材質に比べて接着性
および耐食性に優れた塩基性質溶射材を得ることができ
る。これは、以下の理由によるものと考えられる。本発
明で使用する焼結カルシア−マグネシアクリンカーは、
Fe2 O3 成分を1.8〜7wt%を含む。そして、F
e2 O3 を含むことで、溶射材に同時に配合された溶剤
としてのスラグとのなじみがよく、溶射材の接着性が向
上する。According to the present invention, it is possible to obtain a basic spray material having excellent adhesiveness and corrosion resistance as compared with conventional materials. This is considered to be due to the following reasons. The sintered calcia-magnesia clinker used in the present invention is:
The Fe 2 O 3 component containing 1.8~7wt%. And F
By containing e 2 O 3 , it is well compatible with slag as a solvent that is simultaneously mixed with the thermal spray material, and the adhesiveness of the thermal spray material is improved.
【0009】クリンカーに特定量のFe2 O3 成分を含
ませることによって接着性の向上を図る点は、前記特開
昭63−107872号公報に示された石灰質クリンカ
ーと同じ考え方である。しかし、石灰質クリンカーの場
合、その主成分であるCaOがFe2 O3 と反応し、C
aO・Fe2 O3 、2CaO・Fe2 O3 あるいはCa
O・2Fe2 O3 などの低融点物質を生成し、骨材自身
の耐食性の低下のために溶射材の耐食性が大幅に低下す
る。The idea of improving the adhesiveness by including a specific amount of Fe 2 O 3 component in the clinker is the same idea as the calcareous clinker disclosed in the above-mentioned JP-A-63-107872. However, in the case of calcareous clinker, its main component, CaO, reacts with Fe 2 O 3 and C
aO.Fe 2 O 3 , 2CaO.Fe 2 O 3 or Ca
Generates a low melting point substance such as O · 2Fe 2 O 3, the corrosion resistance of the thermal spray material is greatly reduced due to the reduction of the bone material itself corrosion resistant.
【0010】これに対し本発明で使用する焼結カルシア
−マグネシアクリンカーは、成分中にCaOに比べて融
点の高いMgOを18〜63wt%含むことで、Fe2
O3に起因した低融点物質の生成が抑制される。その結
果、耐食性を低下させることなく、Fe2 O3 を含むこ
とによる接着性の向上を図ることができる。また、通常
の焼結カルシア−マグネシアクリンカーは、MgOの熱
膨張係数が大きいことで、スポーリングによるハクリ損
傷を生じる問題がある。溶射材の施工体は緻密質である
ことから、熱膨張によるスポーリングは顕著である。こ
れに対して本発明で使用する焼結カルシア−マグネシア
クリンカーは、Fe2 O3 成分による熱衝撃緩衝作用に
よって、耐スポーリング性の低下を防止する効果もあ
る。On the other hand, the sintered calcia-magnesia clinker used in the present invention contains 18 to 63 wt% of MgO having a melting point higher than that of CaO in the component, and thus, Fe 2
Generation of a low-melting substance due to O 3 is suppressed. As a result, it is possible to improve the adhesion by including Fe 2 O 3 without lowering the corrosion resistance. In addition, ordinary sintered calcia-magnesia clinker has a problem of causing peeling damage due to spalling due to a large thermal expansion coefficient of MgO. Since the sprayed material is dense, spalling due to thermal expansion is remarkable. On the other hand, the sintered calcia-magnesia clinker used in the present invention also has an effect of preventing a decrease in spalling resistance due to the thermal shock buffering action of the Fe 2 O 3 component.
【0011】[0011]
【発明の実施の形態】本発明では、化学成分でCaO:
35〜80wt%、MgO:18〜63wt%、Fe2
O3 :1.8〜7wt%を含み、前記CaOとMgOの
合量93wt%以上の焼結カルシア−マグネシアクリン
カーを5〜40wt%配合する。本発明で使用する前記
焼結カルシア−マグネシアクリンカーの化学成分の割合
は溶射材の特性に影響する。すなわち、CaOが35w
t%未満またはMgOが63wt%を超えた場合は溶射
材の耐スラグ浸透性および耐スポーリング性に劣る。M
gOが18wt%未満またはCaOが80wt%を超え
た場合は耐食性および耐消化性に劣る。前記のCaOと
MgOの合量が93wt%未満では耐食性に劣る。BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, the chemical component is CaO:
35 to 80 wt%, MgO: 18 to 63 wt%, Fe 2
O 3 : 1.8 to 7 wt%, and 5 to 40 wt% of a sintered calcia-magnesia clinker having a total amount of 93 wt% or more of CaO and MgO. The proportion of the chemical component of the sintered calcia-magnesia clinker used in the present invention affects the properties of the thermal spray material. That is, CaO is 35w
When the content is less than t% or the content of MgO exceeds 63% by weight, the slag penetration resistance and the spalling resistance of the sprayed material are inferior. M
When gO is less than 18 wt% or CaO exceeds 80 wt%, the corrosion resistance and digestion resistance are poor. If the total amount of CaO and MgO is less than 93 wt%, the corrosion resistance is poor.
【0012】また、本発明で使用する前記焼結カルシア
−マグネシアクリンカーの化学成分において、Fe2 O
3 の割合が1.8wt%未満では接着性に劣り、7wt
%を超えると耐食性に劣る。Fe2 O3 のさらに好まし
い範囲は、2〜7wt%である。焼結カルシア−マグネ
シアクリンカーは、合成品と天然品がある。合成品は海
水等から得た水酸化マグネシウムに消石灰を加えて製造
されるが、本発明で使用する焼結カルシア−マグネシア
クリンカーは、Fe2 O3 成分の添加でFe2 O 3 が
1.8〜7wt%の範囲になるように調整する。天然品
の製造はドロマイト鉱を焼結して製造されるが、本発明
で使用するものはこれにFe2 O3 成分を添加し、Fe
2 O3 が1.8〜7wtの範囲になるように調整する。
焼結温度は合成品、天然品ともに約1700〜2000
℃が好ましい。Further, the sintered calcia used in the present invention is
-In the chemical composition of the magnesia clinkerTwoO
ThreeIs less than 1.8 wt%, the adhesiveness is poor, and 7 wt%
%, The corrosion resistance is poor. FeTwoOThreeEven more preferred
The optimum range is 2 to 7 wt%. Sintered calcia-magne
There are synthetic and natural products. Synthetic products are sea
Manufactured by adding slaked lime to magnesium hydroxide obtained from water etc.
The sintered calcia-magnesia used in the present invention
The clinker is FeTwoOThreeFe by adding the componentTwoO ThreeBut
Adjust so as to be in the range of 1.8 to 7 wt%. Natural products
Is manufactured by sintering dolomite ore.
What is used in this is FeTwoOThreeAdd the ingredients and add Fe
TwoOThreeIs adjusted to be in the range of 1.8 to 7 wt.
The sintering temperature is about 1700-2000 for both synthetic and natural products
C is preferred.
【0013】前記の焼結カルシア−マグネシアクリンカ
ーは、付着性および耐食性の効果を持つが、これのみで
は耐食性が不十分である。本発明では、耐食性付与のた
めに、焼結マグネシアクリンカーおよび/または電融マ
グネシアを組み合わせる。焼結マグネシアクリンカーあ
るいは電融マグネシアは、MgO純度が高いことが好ま
しいが、高純度品は価格が高いので、MgO純度が85
wt%以上のものの中から経済性などを考慮して使用す
る。The above-mentioned sintered calcia-magnesia clinker has effects of adhesion and corrosion resistance, but the corrosion resistance alone is insufficient. In the present invention, sintered magnesia clinker and / or electrofused magnesia are combined for imparting corrosion resistance. Sintered magnesia clinker or electrofused magnesia preferably has a high MgO purity, but a high-purity product is expensive.
It is used in consideration of economy and the like from those of wt% or more.
【0014】スラグの種類は転炉スラグ、高炉スラグ、
電気炉スラグ、脱硫スラグなどがあり、これらの中から
選択使用する。化学成分的にはSiO2 、CaO、Fe
2 O 3 、Al2 O3 などを主成分とする。溶射材に占め
る割合は、10wt%未満では付着性に劣り、50wt
%を超えると耐食性が低下する。前記した焼結カルシア
−マグネシアクリンカーと、焼結マグネシアクリンカー
および/または電融マグネシア以外の耐火原料を、30
wt%以下の範囲で配合してもよい。その具体例は、ク
ロム鉱、アルミナ、シリカ、アルミナ−シリカ、ジルコ
ン、ジルコニア、スピネル、炭素、炭化物、窒化物、酸
化リチウム、チタニア、シリコンなどである。また、F
e2 O3 の含有量が1.8%未満または7%を超える焼
結カルシア−マグネシアクリンカーでもよい。The types of slag are converter slag, blast furnace slag,
There are electric furnace slag, desulfurization slag, etc.
Select to use. Chemical composition is SiOTwo, CaO, Fe
TwoO Three, AlTwoOThreeEtc. as a main component. Occupy spray material
If the ratio is less than 10 wt%, the adhesion is poor, and 50 wt%
%, The corrosion resistance decreases. Sintered calcia mentioned above
Magnesia clinker and sintered magnesia clinker
And / or refractory raw materials other than fused magnesia
You may mix | blend in the range of wt% or less. An example is
Lombite, alumina, silica, alumina-silica, zircon
, Zirconia, spinel, carbon, carbide, nitride, acid
Lithium oxide, titania, silicon and the like. Also, F
eTwoOThreeWith less than 1.8% or more than 7%
It may be a calcia-magnesia clinker.
【0015】溶融助剤として、スラグ以外にもオリビ
ン、ワラストナイトなどを組合せ使用してもよい。しか
し、スラグとの合量において10〜50wt%の範囲を
超えないことが必要である。以上の各配合物の粒径は、
従来の溶射材と同様、ノズルからの噴出性、火炎による
溶融性などを考慮して1mm以下、好ましくは平均50
〜150μmとする。溶射方法は従来どおり、プロパン
ガス、アセチレン、水素、灯油などを燃料とする溶射機
を用いて行う。本発明の火炎溶射材は、例えば転炉、溶
解炉、AOD炉、取鍋、タンデッシュ、真空脱ガス炉、
混銑車、電気炉、焼却炉、誘導炉、加熱炉などの工業窯
炉の内張り形成、内張りに対する被覆または補修の他、
耐火物品の形成、被覆、補修などにも使用できる。As a melting aid, olivine, wollastonite and the like may be used in combination other than slag. However, it is necessary that the total amount with the slag does not exceed the range of 10 to 50 wt%. The particle size of each of the above compounds is
As in the case of the conventional thermal spraying material, the thickness is 1 mm or less, preferably 50 mm in average, in consideration of the jetting property from the nozzle and the melting property by the flame.
To 150 μm. Conventionally, the thermal spraying method is performed using a thermal spraying machine using propane gas, acetylene, hydrogen, kerosene or the like as a fuel. The flame sprayed material of the present invention is, for example, a converter, a melting furnace, an AOD furnace, a ladle, a tundish, a vacuum degassing furnace,
In addition to forming and repairing the lining of industrial kilns such as mixed iron cars, electric furnaces, incinerators, induction furnaces, and heating furnaces,
It can also be used for forming, coating and repairing refractory articles.
【0016】[0016]
【実施例】表1は、実施例および比較例で使用した各配
合物の化学成分を示すものである。表2は、実施例およ
び比較例の溶射材の配合組成とその試験結果である。図
1は、表2に示す実施例1の配合組成の溶射材をベース
とし、配合組成中の焼結カルシア−マグネシアクリンカ
ーのFe2 O3 成分のみを変化させ、焼結カルシア−マ
グネシアクリンカー中のFe2 O3 成分と溶射材の接着
性との関係を示したグラフである。EXAMPLES Table 1 shows the chemical components of each compound used in Examples and Comparative Examples. Table 2 shows the compositions of the thermal spray materials of the examples and comparative examples and the test results. FIG. 1 is based on the thermal sprayed material of the composition of Example 1 shown in Table 2, and changes only the Fe 2 O 3 component of the sintered calcia-magnesia clinker in the composition. 4 is a graph showing the relationship between the Fe 2 O 3 component and the adhesiveness of the thermal spray material.
【0017】溶射にはいずれもプロパン−酸素の火炎溶
射装置を使用した。火炎温度は最高温度部位で約250
0℃であった。溶射材は平均粒径88〜90μmに調整
し、3Kg/minの速度で火炎中に供給した。被溶射
面は、表面温度を約1200℃に加熱したMgO−C質
レンガの垂直壁とした。表2に示す試験は、溶射体を溶
射面に付着した状態で切り出し、以下に示す方法で行っ
た。For the thermal spraying, a propane-oxygen flame spraying apparatus was used. Flame temperature is about 250 at the highest temperature
It was 0 ° C. The sprayed material was adjusted to an average particle size of 88 to 90 μm and supplied into the flame at a rate of 3 kg / min. The surface to be sprayed was a vertical wall of MgO-C brick having a surface temperature of about 1200 ° C. The test shown in Table 2 was performed by cutting out the sprayed body in a state where the sprayed body was attached to the sprayed surface, and performing the following method.
【0018】接着性;1200℃の電気炉内で溶射面と
溶射材とのせん断強度を求めた。 耐食性;溶射体を回転侵食して溶損寸法を求めた。侵食
剤は鋼片と転炉スラグを重量比1:1で組合せたものと
した。 耐スポーリング性;溶射体を電気炉中で1500℃×2
0min加熱後、強制的に空冷し、亀裂発生の状況を目
視により観察した。Adhesion: The shear strength between the sprayed surface and the sprayed material was determined in an electric furnace at 1200 ° C. Corrosion resistance: The sprayed body was rotationally eroded to determine the erosion dimension. The erosion agent was a combination of steel slab and converter slag at a weight ratio of 1: 1. Spalling resistance; 1500 ° C x 2 sprayed material in electric furnace
After heating for 0 min, the mixture was forcibly air-cooled and the state of crack generation was visually observed.
【0019】実機試験;MgO−C質レンガで内張りし
た100t転炉を火炎溶射で補修し、その後の耐用チャ
ージ数を求めた。その際、溶射材の火炎中への供給速度
は、35〜45Kg/minとした。Actual test: A 100 t converter lined with MgO-C brick was repaired by flame spraying, and then the number of usable charges was determined. At that time, the supply rate of the thermal spray material into the flame was 35 to 45 Kg / min.
【0020】[0020]
【表1】 [Table 1]
【0021】[0021]
【表2】 [Table 2]
【0022】図1のグラフから、焼結カルシア−マグネ
シアクリンカー中のFe2 O3 が接着性の向上に効果が
あることが確認できる。また、表2に示す試験結果のと
おり、本発明実施例は接着性、耐食性および耐スポーリ
ング性を兼ね備え、実機試験においては優れた補修効果
が得られた。これに対し、Fe2 O3 の含有量が本発明
の限定範囲より少ない合成焼結マグネシア−カルシアク
リンカーを配合した比較例1と、Fe2 O3 の含有量が
本発明の限定範囲より少ない天然焼結マグネシア−カル
シアクリンカーを配合した比較例2は、接着性および耐
スポーリング性に劣る。Fe2 O3 添加の焼結カルシア
クリンカーを配合した比較例3、スラグの割合が多過ぎ
る比較例4、Fe2O3 添加の合成焼結マグネシア−カ
ルシアクリンカーの割合が多過ぎる比較例5は、耐食性
に劣る。Fe2 O3 添加の天然焼結マグネシア−カルシ
アクリンカーの割合が少ない比較例6は、接着性に劣
る。Fe2 O3 の含有量が本発明の限定範囲より多い天
然焼結マグネシア−カルシアクリンカーを配合した比較
例7は、接着性には優れるが、耐食性に劣る。From the graph of FIG. 1, it can be confirmed that Fe 2 O 3 in the sintered calcia-magnesia clinker is effective in improving the adhesiveness. Further, as shown in the test results shown in Table 2, the examples of the present invention had both adhesiveness, corrosion resistance, and spalling resistance, and an excellent repair effect was obtained in an actual machine test. In contrast, small synthetic sintered magnesia than the limited range of the content of Fe 2 O 3 is the invention - as calcia Comparative Example 1 The clinker blended, less natural than the limited range of the content of Fe 2 O 3 is the invention Comparative Example 2 in which the sintered magnesia-calcia clinker was blended was inferior in adhesion and spalling resistance. Fe 2 O 3 Comparative blended sintered calcia clinker additives example 3, synthesis sintered magnesia of Comparative Example 4, Fe 2 O 3 addition ratio of the slag is too high - calcia clinker Comparative Example 5 ratio is too high the car, Poor corrosion resistance. Comparative Example 6, in which the proportion of natural sintered magnesia-calcia clinker to which Fe 2 O 3 was added was small, was poor in adhesion. Comparative Example 7, in which a natural sintered magnesia-calcia clinker in which the content of Fe 2 O 3 is larger than the limited range of the present invention, is excellent in adhesion, but inferior in corrosion resistance.
【0023】[0023]
【発明の効果】以上の実施例の試験結果が示すように、
本発明によると、接着性、耐食性および耐スポーリング
性を兼ね備えた溶射材を得ることができる。その結果、
例えば各種溶融金属用窯炉の補修材として本発明の溶射
材を使用すれば、炉の耐用性の向上による補修工数およ
び補修材の低減、さらには炉の稼動率向上などの効果を
得ることができ、きわめて有益である。As shown in the test results of the above examples,
According to the present invention, it is possible to obtain a thermal sprayed material having both adhesiveness, corrosion resistance and spalling resistance. as a result,
For example, if the sprayed material of the present invention is used as a repair material for various kinds of molten metal kilns, effects such as a reduction in repair man-hours and repair materials by improving the durability of the furnace, and further, an improvement in furnace operation rate can be obtained. Can and is very useful.
【図1】焼結カルシア−マグネシアクリンカー中に占め
るFe2 O3 成分の割合と溶射材の接着性との関係を示
したグラフである。FIG. 1 is a graph showing the relationship between the ratio of a Fe 2 O 3 component in a sintered calcia-magnesia clinker and the adhesiveness of a thermal spray material.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 村上 角一 兵庫県高砂市荒井町新浜1丁目3番1号 ハリマセラミック株式会社内 (72)発明者 久保 寛明 兵庫県高砂市荒井町新浜1丁目3番1号 ハリマセラミック株式会社内 ──────────────────────────────────────────────────続 き Continuing from the front page (72) Kakuichi Murakami 1-3-1 Shinhama, Arai-machi, Takasago City, Hyogo Prefecture Inside Harima Ceramics Co., Ltd. (72) Hiroaki Kubo 1-3-1, Shinhama, Arai-machi, Takasago City, Hyogo Prefecture No. Harima Ceramics Co., Ltd.
Claims (2)
gO:18〜63wt%、Fe2 O3 :1.8〜7wt
%を含み、前記CaOとMgOの合量が93wt%以上
の焼結カルシア−マグネシアクリンカーを5〜40wt
%と、焼結マグネシアクリンカーおよび/または電融マ
グネシアを30〜70wt%と、スラグ10〜50wt
%とを配合した火炎溶射材。1. A chemical composition of CaO: 35-80 wt%, M
gO: 18~63wt%, Fe 2 O 3: 1.8~7wt
%, And the total amount of CaO and MgO is 93 wt% or more.
%, 30 to 70 wt% of sintered magnesia clinker and / or electrofused magnesia, and 10 to 50 wt% of slag.
%.
gO:18〜63wt%、Fe2 O3 :1.8〜7wt
%を含み、前記CaOとMgOの合量が93wt%以上
の焼結カルシア−マグネシアクリンカーを5〜40wt
%と、焼結マグネシアクリンカーおよび/または電融マ
グネシアを30〜70wt%と、前記以外の耐火原料3
0wt%以下と、スラグ10〜50wt%とを配合した
火炎溶射材。2. The chemical composition of CaO: 35-80 wt%, M
gO: 18~63wt%, Fe 2 O 3: 1.8~7wt
%, And the total amount of CaO and MgO is 93 wt% or more.
%, Sintered magnesia clinker and / or electrofused magnesia in an amount of 30 to 70 wt%,
A flame sprayed material containing 0 wt% or less and slag of 10 to 50 wt%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23098897A JP3982647B2 (en) | 1997-08-27 | 1997-08-27 | Flame spraying material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23098897A JP3982647B2 (en) | 1997-08-27 | 1997-08-27 | Flame spraying material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH1171183A true JPH1171183A (en) | 1999-03-16 |
JP3982647B2 JP3982647B2 (en) | 2007-09-26 |
Family
ID=16916483
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JP23098897A Expired - Fee Related JP3982647B2 (en) | 1997-08-27 | 1997-08-27 | Flame spraying material |
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JP (1) | JP3982647B2 (en) |
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1997
- 1997-08-27 JP JP23098897A patent/JP3982647B2/en not_active Expired - Fee Related
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Publication number | Publication date |
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JP3982647B2 (en) | 2007-09-26 |
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