Highly selective recovery of rare earth elements from mining wastewater using phyto-synthesized biochar dispersed iron nanoparticles

生物炭 废水 稀土 纳米颗粒 废物管理 污水处理 环境科学 化学工程 化学 环境化学 材料科学 纳米技术 环境工程 矿物学 工程类 热解
作者
Yalin Yang,Wenli Liu,Xiulan Weng,Zhibiao Chen,Gary Owens,Zuliang Chen
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:353: 128491-128491 被引量:7
标识
DOI:10.1016/j.seppur.2024.128491
摘要

Recovery of rare earth elements (REEs) from secondary sources such as mining wastewater has attracted much recent attention due to the rising global demand for REEs and the need to environmentally protect potentially contaminated mine sites. One significant issue it that most adsorbents proposed for removal and/or recovery of REEs are not generally selective for REEs. In this study, biochar dispersed iron nanoparticles synthesized using a plant extract (BC-FeNPs) were successfully used for the selective recovery of REEs from mining wastewater, where the Kd values were Nd(III) (918 mL∙g−1), Eu(III) (1253 mL∙g−1), Tb(III) (1119 mL∙g−1), Dy(III) (1032 mL∙g−1), Lu(III) (1898 mL∙g−1), compared to only 23.9 mL∙g−1 for Zn(II). The maximum adsorption efficiency of REEs for the composite was higher than the constituent parts being 88.4 % for BC-FeNPs, but only 8.72 % for biochar and 82.4 % for FeNPs, respectively. FTIR, XPS and Zeta potential analysis suggested that the observed selective adsorption of REEs, involved interactions of REEs with O and N, as well as ion-exchange with H+ from the biochar and capping layer, as well as electrostatic interactions. The desorption efficiency of bound REEs from BC-FeNPs was > 85 % when using acetic acid, and was attributed to efficient competitive ion exchange. Pearson correlation analysis further demonstrated that the adsorption mechanism included ion complexation, ion exchange and electrostatic adsorption, while the desorption mechanism was mainly via ion exchange. Overall, BC-FeNPs has significant potential to practically recover REEs from mining wastewater having demonstrated excellent reusability after five adsorption–desorption cycles.
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