Efficient removal of mercury ions with MoS2-nanosheet-decorated PVDF composite adsorption membrane

被引:59
作者
Zhao, Xinghua [1 ]
Li, Jing [2 ]
Mu, Shuyong [1 ]
He, Wei [2 ]
Zhang, Dan [3 ]
Wu, Xia [2 ]
Wang, Chuanyi [3 ]
Zeng, Hehua [2 ]
机构
[1] Chinese Acad Sci, Serv Ctr Publ Technol, Xinjiang Inst Ecol & Geog, Urumqi 830011, Peoples R China
[2] Changji Univ, Dept Chem & Appl Chem, Changji 831100, Xinjiang, Peoples R China
[3] Shaanxi Univ Sci & Technol, Sch Environm Sci & Engn, Xian 710021, Peoples R China
基金
中国国家自然科学基金;
关键词
Adsorption membrane; MoS2; PVDF; Mercury; Recyclability; SELECTIVE REMOVAL; WASTE-WATER; HIGHLY EFFICIENT; HIGH-PERFORMANCE; HEAVY-METALS; HG(II); HG2+; NANOCOMPOSITE; REMEDIATION; SORBENTS;
D O I
10.1016/j.envpol.2020.115705
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The exploitation of a new adsorbent with a high adsorption performance and recyclability is of great practical significance for the treatment of wastewater containing mercury ions. In this study, a novel membrane adsorbent was fabricated by blending MoS2 nanosheets into a PVDF polymer matrix (P-PVDF/MoS2) followed by non-solvent-induced phase conversion. This material was able to bind mercury ions and was not affected by the solution ionic strength, co-existing anions, or interfering heavy metal ions. The optimal pH range for mercury ion elimination was 4.5-6.0, and P-PVDF/MoS2 exhibited a maximum adsorption capacity of 578 mg g(-1). The pseudo-second-order adsorption kinetics and Langmuir isotherm models best described the adsorption process. The adsorption mechanism was mainly monolayer chemisorption, for which the S groups were the major active sites. Furthermore, the membrane could be removed from the aqueous solution easily using tweezers, and the removal efficiency of mercury ions remained over 90% after ten cycles. This study suggests that the inexpensive and recyclable P-PVDF/MoS2 membranes can be used for the efficient removal of heavy metal ions from wastewater at a large scale. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:10
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