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Mechanism of vanadium leaching during surface weathering of basic oxygen furnace steel slag blocks: a microfocus x-ray absorption spectroscopy and electron microscopy study

机译:碱性氧气炉钢渣块表面风化过程中钒的浸出机理:微焦点x射线吸收光谱和电子显微镜研究

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摘要

Basic oxygen furnace (BOF) steelmaking slag is enriched in potentially toxic V which may become mobilized in high pH leachate during weathering. BOF slag was weathered under aerated and air-excluded conditions for 6 months prior to SEM/EDS and μXANES analysis to determine V host phases and speciation in both primary and secondary phases. Leached blocks show development of an altered region in which free lime and dicalcium silicate phases were absent and Ca–Si–H was precipitated (CaCO3 was also present under aerated conditions). μXANES analyses show that V was released to solution as V(V) during dicalcium silicate dissolution and some V was incorporated into neo-formed Ca–Si–H. Higher V concentrations were observed in leachate under aerated conditions than in the air-excluded leaching experiment. Aqueous V concentrations were controlled by Ca3(VO4)2 solubility, which demonstrate an inverse relationship between Ca and V concentrations. Under air-excluded conditions Ca concentrations were controlled by dicalcium silicate dissolution and Ca–Si–H precipitation, leading to relatively high Ca and correspondingly low V concentrations. Formation of CaCO3 under aerated conditions provided a sink for aqueous Ca, allowing higher V concentrations limited by kinetic dissolution rates of dicalcium silicate. Thus, V release may be slowed by the
机译:碱性氧气炉(BOF)炼钢炉渣富含潜在的有毒V,其在风化过程中可能在高pH渗滤液中动员。在进行SEM / EDS和μXANES分析之前,将BOF炉渣在曝气和空气排除条件下风化6个月,以确定初级和次级相中的V宿主相和形态。浸出的块显示出变化区域的发展,其中没有游离石灰和硅酸二钙相,并且沉淀了Ca–Si–H(在充气条件下也存在CaCO3)。 μXANES分析表明,在硅酸二钙溶解过程中,V以V(V)的形式释放到溶液中,并且某些V被掺入新形成的Ca–Si–H中。在曝气条件下,渗滤液中的V浓​​度要高于空气排除浸出实验中的V浓度。 V水溶液的浓度受Ca3(VO4)2溶解度的控制,这表明Ca和V浓度之间呈反比关系。在空气排除条件下,钙的浓度受硅酸二钙溶解和Ca–Si–H沉淀的控制,从而导致较高的Ca和相应的低V浓度。在充气条件下形成CaCO3为Ca水溶液提供了一个汇,使较高的V浓度受到硅酸二钙动力学溶解速率的限制。因此,V的释放可能会因

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