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利用微焦 X 射线吸收光谱和电子显微镜研究碱性氧气炉渣块表面风化过程中钒的浸出机理。

Mechanism of Vanadium Leaching during Surface Weathering of Basic Oxygen Furnace Steel Slag Blocks: A Microfocus X-ray Absorption Spectroscopy and Electron Microscopy Study.

机构信息

School of Animal, Rural and Environmental Sciences, Nottingham Trent University , Brackenhurst Campus, Southwell, Nottinghamshire NG25 0QF, U.K.

School of Environmental Sciences, University of Hull , Hull, HU6 7RX, U.K.

出版信息

Environ Sci Technol. 2017 Jul 18;51(14):7823-7830. doi: 10.1021/acs.est.7b00874. Epub 2017 Jul 6.

Abstract

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 (CaCO 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 Ca(VO) 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 CaCO 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 precipitation of secondary phases in the altered region, improving the prospects for slag reuse.

摘要

碱性氧气转炉(BOF)炼钢渣富含潜在毒性的 V,在风化过程中,高 pH 值浸出液中 V 可能变得具有流动性。在进行扫描电子显微镜/能谱分析(SEM/EDS)和微 X 射线吸收近边结构分析(μXANES)之前,将 BOF 渣在充气和不充气条件下风化 6 个月,以确定初级和次级相中 V 的主要宿主相和形态。浸出块显示出变质区的发育,其中游离石灰和硅酸二钙相不存在,Ca-Si-H 沉淀(在充气条件下也存在 CaCO)。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,一些 V 被纳入新形成的 Ca-Si-H。在充气条件下的浸出液中观察到的 V 浓度高于不充气浸出实验。水溶 V 浓度受 Ca(VO)溶解度的控制,表明 Ca 和 V 浓度之间存在反比关系。在不充气条件下,Ca 浓度受硅酸二钙溶解和 Ca-Si-H 沉淀的控制,导致 Ca 浓度较高,相应的 V 浓度较低。在充气条件下形成的 CaCO 为水溶 Ca 提供了一个汇,从而限制了硅酸二钙的动力学溶解速率,允许更高的 V 浓度。因此,通过变质区次生相的沉淀,V 的释放可能会减缓,从而改善渣的再利用前景。

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