Efficient and Selective Removal of Hg(II) from Aqueous Solution by a Highly Stable Amino Isonicotinic-Based Coordination Polymer

被引:4
作者
Shao, Zhichao [1 ]
Yan, Yangshuang [1 ]
Wei, Yi [2 ,3 ]
Gao, Kexin [1 ,3 ]
Cheng, Haoran [1 ]
Xue, Xiaojing [2 ]
Hou, Hongwei [2 ,3 ]
机构
[1] Zhongyuan Univ Technol, Ctr Adv Mat Res, Zhengzhou 450007, Henan, Peoples R China
[2] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Henan, Peoples R China
[3] Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Henan, Peoples R China
基金
中国博士后科学基金;
关键词
METAL-ORGANIC FRAMEWORK; HEAVY-METALS; ADSORPTION; HG2+; WASTEWATERS; PERFORMANCE; FABRICATION; ADSORBENT; MERCURY; IONS;
D O I
10.1021/acs.cgd.3c00923
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of a stable, efficient, and highly selective Hg(II) adsorbent is important for sewage treatment and for human health. This study presents a new isonicotinic acid-based coordination polymer (CP-1-NH2), investigates its Hg(II) removal performance, and proposes a mechanism of Hg(II) removal by CP-1-NH2. A large number of uncoordinated amino groups are retained during the formation of the coordination framework with nicotinic acid groups, enabling the selective and efficient capture of Hg2+ ions. The maximum adsorption capacity is 116.32 mg/g. The environmentally friendly ligands avoid secondary pollution caused by S-containing compounds. CP-1-NH2 also resists interference by coexisting ions in aqueous solutions. CP-1-NH2 demonstrated a high removal performance during the entire adsorption process, which occurs in a single-crystal state. The regeneration performance was retained after multiple cycles. The possible adsorption mechanism was systematically verified through Fourier transform infrared transform and X-ray photoelectron spectroscopies. The amino-functionalized materials exhibit a high affinity for Hg(II). This work provides new design considerations for crystalline metal-organic framework adsorbents.
引用
收藏
页码:8809 / 8817
页数:9
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