摘要
以高温氧化性炉渣为电解质,工业MgO-C砖为阴极,钼丝为阳极,研究外电场作用下耐火材料在CaO-SiO_2-FeO三元氧化性渣中的侵蚀行为。结果表明:在CaO-SiO_2-FeO渣中,Si的还原电位约为-5.85V,Fe的还原电位约为-1.25V;当外加电压小于炉渣中离子还原电位时,电压趋使炉渣中离子(Fe~(2+),Ca~(2+))向阴极作定向移动,而SiO_4~(2-)由于离子半径大,移动速度较慢,大部分滞留在阴极区域,使得阴极附近熔渣粘度不断增加,有效降低了炉渣渗透深度;当阴极电位低于炉渣中离子还原电位时,炉渣中Fe~(2+)和SiO_4~(2-)将发生电化学还原,Fe和Si的析出促使熔渣组成发生变化,诱导高熔点相硅酸二钙沉积层的形成。高熔点沉积层有效阻断炉渣与耐火材料直接接触,使得熔渣在耐火材料中的渗透深度显著降低,提高了耐火材料抗渣侵能力。
Corrosion behavior of MgO-C refractory in molten oxide slag was investigated under applied voltage,during which MgO-C brick worked as the cathode and molybdenum as anode,..The results show that the reduction potential of SiO_4~(2-)and Fe~(2+)are about-5.85 and-1.25 Vin the CaO-SiO_2-FeO system,respectively.When the voltage is applied,ions(Ca~(2+)and Fe~(2+))move to the cathode and aggregate around the cathode.Meanwhile,SiO_4~(2-)ions move to the anode relatively slowly because of their big radius,which results in the retention of SiO_4~(2-)anions at the cathode range.If the applied voltage is less than the reduction potential of the slag,the aggregated ions can lead to viscosity increase of slag around the cathode,which hinders s the diffusion of slag into the MgO-C refractory and thus leads to the decrease in penetration depth.When the applied voltage is lower than the reduction potential of Fe~(2+)and SiO_4~(2-),metallic Si or Fe is formed,which induces a shift of slag composition toward the high melting products(Ca_2SiO_4).The high melting product layer is responsible for the good physical and chemical protection of the refractory because it blocks the direct contact between the slag and the refractory.
引文
[1]王慧华,徐英君,蒋坤,等.外电场作用下熔渣对MgO-C耐火材料的侵蚀行为[J].材料导报:研究篇,2017,31(10):96~100.
[2]周莉,赵会峰,姜宏.高铝硅酸盐玻璃对耐火材料的侵蚀[J].材料科学与工程学报,2016,34(4):634~637.
[3]陈肇友.钢铁工业用耐火材料的发展动向[J].耐火材料,1994,28(6):309~314.
[4]陈福义,Delbert E D.铁磷和硼硅酸盐熔体对耐火材料的腐蚀性能[J].材料科学与工程学报,2001,19(3):54~59.
[5]徐匡迪.关于洁净钢的若干基本问题[J].金属学报,2009,45(3):257~269.
[6]刘浏.洁净钢生长技术的发展与创[J].中国冶金,2016,26(10):18~28.
[7]Wang D Y,Li X B,Wang H H,et al.Dissolution rate and mechanism of MgO particles in synthetic ladle slags[J].Journal of Non-Crystalline solids,2012,358:1196~1202.
[8]Kazakov A A.Influence of the electrical potential on converter smelting[J].Russian Metallurgy,1997,6(1):25~29.
[9]Siebring R,Franken M C.Effect of applied electric field on slag erosion resistance of MgO refractory[C].Proceedings of 39th International Colloquy on Refractory,Aachen,1996:32~39.
[10]Orejon D,Sefiane K,Shanahan Martin E.R.Young-Lippmann equation revisited for nano-suspensions[J].Applied Physics Letters,2013,102(20):201601~201607.
[11]Li X C,Zhu B Q,Wang T X.Effect of electromagnetic field on slag corrosion resistance of low carbon MgO-C refractory[J].Ceramics International,2012,38(10):2015~2020.
[12]Nightingale S A,Brooks G A,Monaghan B J.Degradation of MgO refractory in CaO-SiO2-MgO-FeOx and CaO-SiO2-Al2O3-MgO-FeOx liquid oxides under forced convection[J].Metallurgical and Materials Transactions B,2005,36(4):453~461.
[13]李享成,王堂玺,姜晓,等.电磁场对MgO-C耐火材料抗渣侵蚀性的影响[J].硅酸盐学报,2011,39(3):452~457.
[14]Riaz S,Mills K C,Bain K.Experimental examination of slag/refractory interface[J].Ironmaking and Steelmaking,2002,29(2):107~113.
[15]Riaz S.Effect of electric potential on mold powder behavior during solidification[J].Ironmaking and Steelmaking,2012,39(6):409~413.
[16]Riaz S,Mills K C.Can the application of electric potential increase refractory life[J].Ceramic Forum International,2002,79(3):47~50.
[17]Monaghan B J,Nightingale S A.The dissolution behavior of select oxides in CaO-SiO2-Al2O3slags[C].ⅦInternational conference on molten Slags and Salts,The South African Institute and Mining and Metallurgy,2004:585~594.
[18]Monaghan B J,Nighingale S A,Dong Q.The effect of an applied voltage on the corrosion characteristics of dense MgO[J].Engineering,2010,2:496~501.