Synthesis of magnetic dithiocarbamate chelating resin and its absorption behavior for ethylenediaminetetraacetic acid copper

被引:12
作者
Yan, Pingfang [1 ,3 ]
Ye, Maoyou [1 ]
Guan, Zhijie [1 ]
Sun, Shuiyu [1 ,2 ]
Guo, Yanping [2 ]
Liu, Jingyong [1 ]
机构
[1] Guangdong Univ Technol, Sch Environm Sci & Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Polytech Environm Protect Engn, Foshan 528216, Peoples R China
[3] Guangdong Ocean Univ, Fac Chem & Environm Sci, Zhanjiang 524000, Peoples R China
关键词
Magnetic dithiocarbamate chelating resin; Ethylenediaminetetraacetic acid copper; Absorption behavior; Absorption mechanism; AQUEOUS-SOLUTION; EFFICIENT REMOVAL; STERIC HINDRANCE; HEAVY-METALS; ADSORPTION; WATER; IONS; CU;
D O I
10.1016/j.psep.2018.12.026
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
As an efficient metal-trapping agent, conventional dithiocarbamate is prone to poor flocculation, and difficult recovery, and it is challenging to reuse it in applications. In our study, to address these problems, a novel and efficient chelating agent was developed in the form of a magnetic dithiocarbamate chelating resin. This resin was used to adsorb EDTA-Cu from wastewater. Furthermore, the Cu absorption mechanism of the new resin was investigated. The magnetic dithiocarbamate chelating resin is a composite polymer material with dithiocarbamate functional groups and a good magnetic response. The resin showed a high Cu removal efficiency of 99.19%, and an improved sedimentation performance. Moreover, the resin can be effectively recycled, and it was reused twice after desorption with 4% thiourea, it retained an absorption rate of 89.95%. The adsorption mechanism was based on chemical adsorption. The sulfur atoms of the resin had coordinated with the Cu of EDTA-Cu and formed a stable coordination compound. This research of the resin not only enriches the metal-trapping agent, but also provides a new idea for treating low concentration complex metal pollutants. (C) 2019 Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:130 / 139
页数:10
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