Jia Feifei, Zhang Xian, Song Shaoxian
Hubei Key Laboratory of Mineral Resources Processing and Environment, Wuhan University of Technology, Luoshi Road 122, Wuhan, Hubei 430070, P. R. China.
School of Resources and Environmental Engineering, Wuhan University of Technology, Luoshi Road 122, Wuhan, Hubei 430070, P. R. China.
Phys Chem Chem Phys. 2017 Feb 1;19(5):3837-3844. doi: 10.1039/c6cp07302f.
The adsorption of Hg on natural molybdenum disulfide has been studied using atomic force microscope (AFM). The AFM imaging clearly illustrated the adsorption of Hg on the surface of molybdenum disulfide, and also hydration layers on the surfaces. It was found that the presence of a hydration layer on molybdenum disulfide surfaces hindered the Hg adsorption. Also, it was observed that the Hg adsorbed appeared in the form of multilayers. The first adsorbed Hg layer might be mainly attributed to the complexation of Hg with S atoms exposed on molybdenum disulfide surfaces, while the second one might be due to the electrostatic interaction between negatively charged molybdenum disulfide and the cation Hg.
利用原子力显微镜(AFM)研究了汞在天然二硫化钼上的吸附情况。AFM成像清晰地显示了汞在二硫化钼表面的吸附,以及表面的水化层。研究发现,二硫化钼表面水化层的存在阻碍了汞的吸附。此外,观察到吸附的汞呈现多层形式。第一层吸附的汞可能主要归因于汞与二硫化钼表面暴露的硫原子的络合作用,而第二层可能是由于带负电的二硫化钼与阳离子汞之间的静电相互作用。