镉
吸附
分馏
同位素
GSM演进的增强数据速率
化学
环境化学
地质学
物理化学
物理
色谱法
工程类
核物理学
有机化学
电信
作者
Hui Yin,Xinran Yan,Chuanwei Zhu,Kideok D. Kwon,Xueyuan Gu,Wei Zhao,Bruno Lanson,Wei Li,Jingyuan Ma,Yan Li,Jiangshan Li,Guohong Qiu,Xionghan Feng,Wenfeng Tan,Hanjie Wen,Qiaoyun Huang,Fan Liu
标识
DOI:10.1021/acs.est.4c03808
摘要
Cadmium (Cd) geochemical behavior is strongly influenced by its adsorption onto natural phyllomanganates, which contain both layer edge sites and vacancies; however, Cd isotope fractionation mechanisms at these sites have not yet been addressed. In the present work, Cd isotope fractionation during adsorption onto hexagonal (containing both types of sites) and triclinic birnessite (almost only edge sites) was investigated using a combination of batch adsorption experiments, extended X-ray absorption fine structure (EXAFS) spectroscopy, surface complexation modeling, and density functional theory (DFT) calculations. Light Cd isotopes are preferentially enriched on solid surfaces, and the isotope fractionation induced by Cd
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