Sato Kiminori, Hunger Michael
Department of Environmental Sciences, Tokyo Gakugei University, Koganei, Tokyo, 184-8501, Japan.
Institute of Chemical Technology, University of Stuttgart, 70550, Stuttgart, Germany.
Commun Chem. 2020 Jul 21;3(1):91. doi: 10.1038/s42004-020-00346-5.
Nanoscale open spaces formed by partial overlap of two-dimensional nanosheets in clays, abundantly and ubiquitously available, possess reactive molecular sites such as nanosheet edges in their interior. Here, the capture and storage of CO molecules in open spaces within saponite clay are explored by solid-state nuclear magnetic resonance coupled with open space analysis using positronium. CO physisorption occurs on the nanosheet surfaces inside the open spaces under ambient conditions. Thereby, CO molecules are activated by picking off weakly-bound oxygen from octahedral sites at the nanosheet edges and carbonate species are stabilized on the nanosheet surfaces. This instantaneous mineral carbonation and CO physisorption occurs in the absence of an energy-consumption process or chemical solution enhancement. This finding is of potential significance for CO capture and storage and presents an approach of environmentally friendly recycling of low contaminated soil in Fukushima.
黏土中二维纳米片部分重叠形成的纳米级开放空间丰富且普遍存在,其内部具有诸如纳米片边缘等反应性分子位点。在此,通过固态核磁共振结合正电子湮没寿命谱的开放空间分析,研究了皂石黏土开放空间中CO分子的捕获和存储。在环境条件下,CO物理吸附发生在开放空间内的纳米片表面。由此,CO分子通过从纳米片边缘的八面体位点夺取弱结合氧而被活化,并且碳酸盐物种在纳米片表面稳定下来。这种瞬时矿物碳化和CO物理吸附在没有能量消耗过程或化学溶液增强的情况下发生。这一发现对CO捕获和存储具有潜在意义,并提出了一种福岛低污染土壤环境友好型循环利用的方法。