砷酸盐
扩展X射线吸收精细结构
氧烷
亚砷酸盐
吸附
热解
吸收(声学)
核化学
X射线吸收精细结构
X射线吸收光谱法
化学
环境化学
六价铬
吸附
水溶液
分析化学(期刊)
材料科学
铬
砷
吸收光谱法
光谱学
物理
有机化学
复合材料
物理化学
量子力学
作者
Yujie Feng,Peng Liu,Yanxin Wang,Y. Zou Finfrock,Xianjun Xie,Chunli Su,Na Liu,Yanyuan Yang,Yong Xu
标识
DOI:10.1016/j.jhazmat.2019.121342
摘要
Characterization of the spatial distribution and speciation of iron (Fe) in Fe-modified biochars is critical for understanding the mechanisms of contaminant removal. Here, synchrotron-based techniques were applied to characterize the spatial distribution and speciation of Fe in biochars modified by FeCl3 or FeSO4 and pyrolyzed at 300, 600, and 900 °C, respectively. Confocal micro-X-ray fluorescence imaging (CMXRFI) results indicated Fe, sulfur (S), and chlorine (Cl) diffused into the basic porous structure of the biochars and aggregated to the surface as pyrolysis temperature increased. Fe K-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectra revealed maghemite (γ-Fe2O3) as the primary Fe species in the modified biochars and Fe(0) was observed when pyrolyzed at 600 or 900 °C. Unmodified and FeCl3-modified biochars pyrolyzed at 900 °C were evaluated in the removal of arsenate (As(V)), arsenite (As(III)), hexavalent chromium (Cr(VI)) and Hg(II) from aqueous solution and Fe-modification enhanced the removal efficiency from 42.0%, 62.5%, 19.6%, and 97.0%, respectively, to all 99.9%. X-ray absorption spectroscopy results indicate both adsorption and redox reaction contributed to the removal mechanisms. The present study provides a prospective and sustainable material and offers information relevant to tailoring Fe-modified biochars to specific environmental applications.
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