Selective removal of aqueous Hg2+ by magnetic composites sulfur-containing on the hyper-branched surface: Characterization, performance and mechanism

吸附 吸热过程 朗缪尔吸附模型 超顺磁性 化学 水溶液 傅里叶变换红外光谱 解吸 打赌理论 水溶液中的金属离子 X射线光电子能谱 核化学 金属 材料科学 化学工程 有机化学 物理 磁化 量子力学 磁场 工程类
作者
Xiangchu Zeng,Guanghua Zhang,Xiuling Li,Junfeng Zhu,Zhe Wu
出处
期刊:Journal of Environmental Management [Elsevier BV]
卷期号:325 (Pt B): 116621-116621 被引量:8
标识
DOI:10.1016/j.jenvman.2022.116621
摘要

The adsorbents with recyclable, large adsorption capacity and selective adsorption can effectively remove the pollution and harm of heavy metal ions in water. Therefore, two magnetic composites containing sulfur (MCP-S4 and MCP-S8) on the hyper-branched surface were prepared, furthermore, their structures were characterized and adsorption performance was analyzed by FTIR, XRD, TGA, BET, SEM, TEM, VSM and ICP. The results showed that both MCP-S4 and MCP-S8 had superparamagnetism with saturation susceptibility of 22.10 and 22.26 emu/g, and owned a specific surface area of 11.394 and 11.235 m2/g, respectively. MCP-S4 and MCP-S8 could selectively adsorb Hg2+ with the exist of Fe3+, Cu2+, Co2+, Ni2+, Mn2+, and Al3+ in solution. The adsorption kinetics accorded with pseudo-second-order model and Boyd film diffusion model, and the adsorption isotherm was fitted better with Langmuir isotherm model and D-R model, furthermore, the adsorption was an entropic-increasing and endothermic process. The removal rate of Hg2+ from simulated sewage by the two materials was more than 91%, and the adsorption retention rate was more than 85% after five adsorption-desorption cycles. The adsorption mechanism was analyzed by comparing the changes of FTIR, EDS and XPS spectra before and after adsorption. It was found that functional groups (C-N, CONH, CS, SH) could form stable chelates with Hg2+, which was the main reason why MCP-S4 and MCP-S8 could adsorb Hg2+ selectively, furthermore, S atoms of CS and -SH played a leading role in the process of adsorption. In addition, DFT calculation was also used as an auxiliary means to verify the adsorption mechanism.
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