Li Zixian, Xu Nuo, Ren Jing, Hao Haigang, Gao Rui, Kong Xianggui, Yan Hong, Hua Xiao, Peng Yung-Kang, Ma Shulan, O'Hare Dermot, Zhao Yufei
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology Beijing 100029 P. R. China
College of Chemistry and Chemical Engineering, Inner Mongolia University 010021 Hohhot Inner Mongolia P. R. China.
Chem Sci. 2024 Jul 19;15(32):13021-13031. doi: 10.1039/d4sc02860k. eCollection 2024 Aug 14.
The environmental concern posed by toxic heavy metal pollution in soil and water has grown. Ca-based layered double hydroxides (LDHs) have shown exceptional efficacy in eliminating heavy metal cations through the formation of super-stable mineralization structures (SSMS). Nevertheless, it is still unclear how the intricate coordination environment of Ca in Ca-based LDH materials affects the mineralization performance, which hinders the development and application of Ca-based LDH materials as efficient mineralizers. Herein, we discover that, in comparison to a standard LDH, the mineralization efficiency for Cd ions may be significantly enhanced in the pentacoordinated structure of defect-containing Ca-5-LDH utilizing both density functional theory (DFT) and molecular dynamics (AIMD) simulations. Furthermore, the calcination-reconstruction technique can be utilized to successfully produce pentacoordinated Ca-5-LDH. Subsequent investigations verified that Ca-5-LDH exhibited double the mineralization performance (421.5 mg g) in comparison to the corresponding pristine seven coordinated Ca-7-LDH (191.2 mg g). The coordination-relative mineralization mechanism of Ca-based LDH was confirmed by both theoretical calculations and experimental results. The understanding of LDH materials and their possible use in environmental remediation are advanced by this research.
土壤和水中有毒重金属污染所引发的环境问题日益严重。钙基层状双氢氧化物(LDHs)通过形成超稳定矿化结构(SSMS)在去除重金属阳离子方面展现出卓越的功效。然而,钙基LDH材料中钙的复杂配位环境如何影响矿化性能仍不清楚,这阻碍了钙基LDH材料作为高效矿化剂的开发与应用。在此,我们利用密度泛函理论(DFT)和分子动力学(AIMD)模拟发现,与标准LDH相比,含缺陷的五配位Ca-5-LDH对镉离子的矿化效率可能会显著提高。此外,煅烧-重构技术可成功制备出五配位的Ca-5-LDH。后续研究证实,与相应的原始七配位Ca-7-LDH(191.2 mg/g)相比,Ca-5-LDH的矿化性能提高了一倍(421.5 mg/g)。理论计算和实验结果均证实了钙基LDH的配位相关矿化机制。这项研究推进了对LDH材料的理解及其在环境修复中的潜在应用。