• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a graphite refractory for continuous casting and an antioxidant applied thereto; The purpose is to prevent oxidation of the graphite refractory. The present invention is applied to the graphite refractory including an antioxidant, including 25 to 50% by weight of feldspar, 25 to 50% by weight of borosilicate glass, 5 to 15% by weight of silicon carbide and 10 to 20% by weight of metal silicon. To form a first coating layer or apply an antioxidant including 2 to 10 parts by weight of metallic aluminum and 25 to 45 parts by weight of silica sol to 100 parts by weight of zircon between the first film and the refractory to form a second film. By forming the film, it is possible to obtain excellent carbon oxidation prevention performance without anti-sparse oxidation or dripping at high temperatures.
    公开号:KR20020039564A
    申请号:KR1020000069469
    申请日:2000-11-22
    公开日:2002-05-27
    发明作者:박재훈；이상암
    申请人:이구택；주식회사 포스코；한종웅；조선내화 주식회사；
    IPC主号:
    专利说明:

    Graphite Refractories for Continuous Casting and Antioxidants Coated Thereon {CARBON CONTAINING REFRACTORY FOR CONTINUOUS CASTING AND OXIDATION PREVENTING COATING MATERIAL THEREON}
    [1] The present invention relates to a continuous casting graphite refractory and a coating agent for the oxidation of the refractory thereof, and more particularly, an antioxidant for forming an antioxidant coating so that oxidation of the continuous casting refractory containing carbon does not occur by heating. And a graphite refractory to which the antioxidant is applied.
    [2] Refractory for continuous casting is required to be resistant to thermal shock and very wet to molten steel and slag in contact with molten steel when the temperature rises very rapidly. Compositions containing carbon, i.e., graphite refractory materials, are used as refractory materials well suited to these required properties.
    [3] Graphite refractories improve the thermal spalling resistance and slag invasion resistance by utilizing the properties of carbon.However, the carbonaceous material forming graphite or bonds is oxidized in an oxidation atmosphere of about 500 ° C. or higher. There are disadvantages. It is also common to preheat before use to mitigate thermal shock.
    [4] In order to prevent the refractory performance from deteriorating due to the oxidation of carbon during heating in the air, conventionally, a means of preventing oxidation by containing a metal in the refractory component or applying a glassy material, that is, an antioxidant to the refractory surface, has been implemented. Antioxidants are used by adjusting the components so that carbon melts above the temperature of about 500 ° C at which coral starts by the atmosphere. That is, as a raw material, water-soluble binders such as sodium silicate, calcium silicate, aluminum phosphate, polyvinyl alcohol, methylcellulose, and dextrin are properly mixed with feldspar-based raw materials or frit or glass powder having a melting temperature of 400 to 700 ° C. The slurry phase is applied to the surface of the carbon-containing refractory and used.
    [5] As a specific example, Japanese Patent Publication No. Hei 5-35709 uses carbonaceous refractory material in which 35 to 60 parts by weight of a composite alkoxide partial hydrolysis sol is added to 100 parts by weight of powder consisting of 50 to 90% by weight of aggregate and 10 to 50% by weight of frit. Antioxidants are described. However, the antioxidant has improved the workability on the surface of the refractory, but when applied to zirconia-graphite in contact with molten steel and molten slag, frit, which is a low melting point component, is melted in a low temperature region, and at high temperature of 1200 ° C. or higher, Iii) the decarburization of tissue due to oxidation has a disadvantage in reducing the content.
    [6] As another example, Japanese Patent Laid-Open No. Hei 5-43354 discloses a mixture of a metal such as transition metal oxide, such as low melting glass Cr, and a liquid binder such as Si, which acts as a glass mesh structure, as a first layer, a low melting glass, and a refractory raw material. And a graphite-containing refractory body that forms a mixture of a liquid binder as a second layer. However, the refractory is oxidized by the transition metal oxide of the metal, which is the network structure of glass in the first layer, to form glass and transition metal, and then to form transition metal carbide, Improves the wettability, but the low melting point of the second layer containing low melting point glass causes the second layer to flow down in the low temperature region, and the first layer also flows down so that it does not exhibit sufficient anti-oxidation function. There is this. In particular, in the case of a thin slab casting nozzle having a thin thickness of the mold, the thickness of the zirconia-graphite refractory is 1/2 or less than that of a general slab nozzle, and thus, such a conventional refractory has a disadvantage of lowering the service life.
    [7] The present invention has been proposed to solve such a conventional problem, and its purpose is not only firmly adhered to the graphite-containing refractory, but also exhibits sufficient anti-oxidation function without flowing out by anti-specular oxidation or melting in the oxidation temperature range of carbon. To provide an antioxidant.
    [8] Further, another object of the present invention is to provide a graphite refractory to which the antioxidant is applied.
    [9] The present invention for achieving the above object comprises a silica sol 40 to 60 parts by weight in 25 to 50% by weight of feldspar, 25 to 50% by weight of borosilicate glass, 5 to 15% by weight of silicon carbide and 10 to 20% by weight of metal silicon The present invention relates to an antioxidant for graphite refractory (hereinafter, referred to as 'antioxidant').
    [10] In addition, the present invention relates to an antioxidant for graphite refractory (hereinafter referred to as 'antioxidant') comprising 2 to 10 parts by weight of metal aluminum and 25 to 45 parts by weight of silica sol in 100 parts by weight of zircon.
    [11] The present invention also relates to a graphite refractory to which the antioxidant is applied.
    [12] Hereinafter, the antioxidant of the present invention will be described in detail.
    [13] First, the antioxidant antioxidant of the present invention comprises silica sol in feldspar, borosilicate glass, silicon carbide and metal silicon. Specifically, the antioxidant agent of the present invention comprises 25 to 50% by weight of feldspar, including 25 to 50% by weight of borosilicate glass, 5 to 15% by weight of silicon carbide and 10 to 20% by weight of silicon silicon. do.
    [14] The feldspar and borosilicate glass are melted at a low temperature of 600 ~ 1000 ℃ to produce a vitrified film to prevent contact with air. That is, feldspar and borosilicate glass as a component that serves to prevent oxygen from invading by contacting the atmosphere during the temperature increase of the refractory layer, the content is preferably limited in the range of 25 to 50% by weight. More preferably, the feldspar and borosilicate glass content are in the range of 65 to 85% by weight. If the content of feldspar and borosilicate glass is too small, the vitrification temperature is not good, and if too much, the viscosity is low at high temperature and it is not good to flow. Even more preferably, the feldspar and borosilicate glass content is maintained at 70 to 80% by weight in total. For example, if the refractory is applied using an oxidizing solution containing feldspar and borosilicate glass in a total amount of 70 to 80% by weight, the softening start temperature is 650 to 700 ° C, and thus a vitrification film is formed at a low temperature. It is good because it does not flow down even high temperature beyond ° C. In addition, the feldspar and the borosilicate glass powder preferably have a particle size of about 0.075 mm or less.
    [15] The silicon carbide and silicon powder are oxidized when contacted with air to produce SiO 2 , as shown in Formulas 1 and 2 during the heating of the refractory. The produced SiO 2 forms a low melting point anti-oxidation coating layer that has a low softening point and does not flow even in a high temperature region of 1500 ° C. by increasing the pour point to prevent the borosilicate glass and the feldspar component from melting and flowing down. For this action, the silicon carbide is preferably contained in the range of 5 to 15% by weight, and in the case of metal silicon, it is preferable to manage in the range of 10 to 20% by weight. Preferably, the silicon carbide and silicon powder have a particle size of about 0.075 mm or less.
    [16] SiC + O 2 → SiO 2 + C
    [17] Si + O 2 → SiO 2
    [18] In addition, the silica sol is a liquid binder and excellent in permeability to the surface of the refractory to produce a hard film at room temperature. The content of the silica sol contained in the main antioxidant is preferably added about 40 to 60 parts by weight to 100 parts by weight of the mixture consisting of feldspar, borosilicate glass, silicon carbide and metal silicon. At this time, it is preferable to use a silica sol containing 20-30% by weight of SiO 2 . The main antioxidant of the present invention mixed in this way is very advantageous for the coating operation as the viscosity of the slurry ranges from about 200 to 3500 cP.
    [19] When applied to the graphite refractory, the antioxidant of the present invention forms a low melting film layer that has a low vitrification point and does not flow in a high temperature region of 1500 ° C. or more to provide a sufficient antioxidant coating in the oxidation region of graphite. Therefore, any antioxidant can be applied as long as it is a graphite refractory material used for continuous casting. It is preferably applied to zirconia-graphite refractory, alumina-graphite refractory or magnesia graphite refractory. If the graphite refractory to be coated for oxidation is alumina or magnesia graphite refractory, it is possible to sufficiently exhibit the antioxidant effect of the refractory material by forming only a single layer by applying only the main antioxidant of the present invention. However, if the graphite refractory is zirconia-graphite refractory, it is preferable to first coat the anti-oxidation agent described below before applying the main antioxidant.
    [20] Here, looking at the anti-scavenging agent of the present invention, the anti-saturation agent of the present invention comprises a zircon, metal aluminum and silica sol. Specifically, the anti-oxidation agent of the present invention comprises 2 to 10 parts by weight of metal aluminum and 25 to 45 parts by weight of silica sol in 100 parts by weight of zircon.
    [21] When the anti-oxidation agent is applied to the zirconia-graphite refractory, the anti-oxidation agent penetrates well into the zirconia-graphite refractory and has a characteristic of preventing semi-specular oxidation at a high temperature of about 1300 ° C or higher. In particular, the first layer is formed by applying the anti-oxidation agent to the zirconia-graphite refractory, and the second layer is formed by applying the main antioxidant on the zirconia-the zircon contained in the first layer is melted at 1550 ℃ or more In addition, aluminum is first oxidized by the atmosphere upon heating to prevent oxidation of zirconia-graphite refractory as well as formation of alumina in the coating layer to form a harder coating so as to prevent anti-stem oxidation in the oxidation temperature range of carbon.
    [22] As the zircon contained in the anti-oxidation agent, it is preferable to use fine powder obtained by grinding zircon yarn to 0.075 mm or less.
    [23] In addition, 2 to 10 parts by weight of metallic aluminum is added to 100 parts by weight of zircon. If the content of aluminum is too small, there is no anti-oxidation effect due to oxidation at the time of heating the refractory, and if too large, excessive pores are formed in the coating layer. This is undesirable because there is a disadvantage that the antioxidant function is reduced.
    [24] In addition, the silica sol, which is a liquid binder, is suitable for containing about 25 to 45 parts by weight of the antioxidant. If the content of the silica sol in the anti-oxidation agent is too small, the viscosity becomes too high, resulting in poor workability. If the amount is too high, the viscosity is low, and the powder and the liquid binder are easily separated, which is difficult to apply. The silica sol is preferably used containing 20 to 30% by weight of SiO 2 , when the silica sol is contained in 25 to 45 parts by weight can be maintained at about 100 ~ 2000cP viscosity of the slurry. Therefore, in this case, when the silica sol is added in about 25 to 35 parts by weight, it is suitable for the coating work by brushing or immersion, and when it is added in about 35 to 45 parts by weight, spray coating is also good.
    [25] Hereinafter, the present invention will be described in detail through examples.
    [26] Example 1
    [27] The heating test was performed about each sample which apply | coated the slurry which has the composition as Table 1 to alumina-graphite refractory, and evaluated the result. In Table 1, the conventional material is an alumina-applied to a case where the addition of the aluminum phosphate, the feldspar in the graphite refractory as Na 2 O-SiO 2 binder, and a curing agent kneaded slurry.
    [28] In the evaluation method, the samples coated with each slurry were heated at 800 ° C. and 1300 ° C. for 1 hour in an air atmosphere, and then cooled after holding for 1 hour. Then, the refractory surface and the film were peeled off and the molten state was observed. The depth of the oxide layer was measured to evaluate the oxidation resistance. In addition, in the case of the invention material (1) (4) and the conventional material, the said slurry was apply | coated to the immersion nozzle for thin slab manufacture preheated at 1250 degreeC, and the actual number of charges used was compared. At this time, the time required for 1charge casting during thin slab manufacturing was about 50 minutes.
    [29] divisionInvention 1Invention 2Invention 3Invention 4Invention 5Conventional Materials 1 feldspar2530303050100 Borosilicate glass4045454525- Silicon Carbide101510510- Metal silicon1510152015- Aluminum phosphate-----10 Na 2 O-SiO 2 Liquid Binder-----70 Silica sol5050545552- Experiment result800 ℃Peel offradishradishradishradishradishradish Oxide layer depth0 mm0 mm0 mm0 mm0 mm0 mm 1300 ℃Molten stateGoodGoodGoodGoodGoodHalf-moon Oxide layer depth0 mm0 mm0 mm0 mm0 mm2 mm charge count10th--10th-5 times
    [30] As shown in Table 1, there was no peeling of the refractory surface and the coating film at 800 ° C in both the conventional materials and the inventive materials (1 to 5). However, in the case of conventional materials, anti-sparse oxidation occurred during the heating test at 1300 ° C, the film flowed down, and oxidation occurred to a depth of about 2 mm, while in the case of the present invention materials (1 to 5), all of the oxide film flowed down at high temperature. It was good without. In addition, as a result of applying to the actual operation, it could be confirmed that the life of the present invention is about twice as long as the present invention.
    [31] On the other hand, except that it was applied to magnesia-graphite refractory instead of alumina-graphite refractory, the same result as the result of evaluating film peeling degree, oxidation degree and the like for magnesia-graphite refractory, showed the same result. Could check.
    [32] Example 2
    [33] A slurry in which 5 parts by weight of metal aluminum and 35 parts by weight of silica sol was mixed to 100 parts by weight of zircon was first applied to the surface of the zirconia-graphite refractory to form a first layer, and then each slurry of Example 1 was applied to The heat test was done about each sample which formed two layers, and the result was evaluated.
    [34] At this time, the evaluation is a feldspar Na 2 O-SiO 2 binder and a zirconia coated with a kneaded slurry was added to the aluminum phosphate as a curing agent - was carried out in the same manner as in Example 1 as compared with the graphite refractory material (conventional material 2). The refractory used in actual operation was invention material (6) (9) and conventional material (2).
    [35] divisionInvention 6Invention 7Invention Material 8Invention Material 9Invention 10Conventional material 2 Experiment result800 ℃Peel offradishradishradishradishradishradish Oxide layer depth0 mm0 mm0 mm0 mm0 mm1 mm 1300 ℃Molten stateGoodGoodGoodGoodGoodSemi-litre oxidation Oxide layer depth0 mm0 mm0 mm0 mm0 mm4mm charge usage10th--10th-5 times
    [36] As shown in Table 2, both the conventional materials and the inventive materials 6 to 10 had no peeling off of the refractory surface and the coating film at 800 ° C., but the conventional material 2 had about 1 mm of oxidation. On the other hand, in the case of the conventional material (2) at 1300 ℃, half-state oxidation occurred during the heating test, the film flowed down and the oxidation occurred to a depth of about 4mm, while in the case of the invention materials (6 to 10), all of the oxide film at a high temperature It was good without dripping. In addition, as a result of applying to the actual operation, it could be confirmed that the life of the present invention is about twice as long as the present invention.
    [37] As described above, the present invention easily penetrates the antioxidant on the surface of the graphite refractory for continuous casting at room temperature, thereby forming a hard film and achieving excellent carbon anti-oxidation performance without anti-sparse oxidation or dripping at high temperatures. It can be effective.
    权利要求:
    Claims (9)
    [1" claim-type="Currently amended] Oxidation of continuous refractory graphite refractory comprising 25 to 50% by weight of feldspar, 25 to 50% by weight of borosilicate glass, 5 to 15% by weight of silicon carbide and 10 to 20% by weight of metal silicon, including 40 to 60 parts by weight of silica sol Inhibitors.
    [2" claim-type="Currently amended] The method of claim 1,
    The feldspar and the borosilicate glass are antioxidants, characterized in that contained in the range of 65 to 85% by weight.
    [3" claim-type="Currently amended] The method of claim 2,
    The feldspar and borosilicate glass are antioxidants, characterized in that contained in the range of 70 to 80% by weight.
    [4" claim-type="Currently amended] An antioxidant comprising 2 to 10 parts by weight of metal aluminum and 25 to 45 parts by weight of silica sol in 100 parts by weight of zircon.
    [5" claim-type="Currently amended] The method according to claim 1 or 4,
    The silica sol is an antioxidant, characterized in that containing 20 to 30% by weight of SiO 2 content.
    [6" claim-type="Currently amended] The method according to claim 1 or 4,
    The antioxidant is an antioxidant, characterized in that the slurry having a particle size of 0.075mm or less.
    [7" claim-type="Currently amended] Graphite refractory for continuous casting in which the antioxidant of claim 1 is applied to form a single coating layer.
    [8" claim-type="Currently amended] The method of claim 7, wherein
    The refractory to which the antioxidant is applied is graphite refractory for continuous casting, characterized in that the alumina-graphite or magnesia-graphite refractory.
    [9" claim-type="Currently amended] Graphite for continuous casting, wherein the antioxidant of claim 1 is applied to a zirconia-graphite refractory to form a first coating layer, and the antioxidant of claim 5 is coated between the first coating layer and the refractory to form a second coating layer. Vaginal refractory.
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    同族专利:
    公开号 | 公开日
    KR100490984B1|2005-05-24|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-11-22|Application filed by 이구택, 주식회사 포스코, 한종웅, 조선내화 주식회사
    2000-11-22|Priority to KR10-2000-0069469A
    2002-05-27|Publication of KR20020039564A
    2005-05-24|Application granted
    2005-05-24|Publication of KR100490984B1
    优先权:
    申请号 | 申请日 | 专利标题
    KR10-2000-0069469A|KR100490984B1|2000-11-22|2000-11-22|Carbon containing refractory for continuous casting and oxidation preventing coating material thereon|
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