Facile synthesis of melamine-based porous polymer networks and their application for removal of aqueous mercury ions

被引:190
作者
Yang, Guangwen [1 ]
Han, Heyou [1 ]
Du, Chunyan [1 ]
Luo, Zhihui [1 ]
Wang, Yanjun [1 ]
机构
[1] Huazhong Agr Univ, Coll Sci, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
Melamine-based polymer; Schiff base chemistry; Mercury; GRAPHITIC CARBON NITRIDE; SOLID-STATE NMR; FORMALDEHYDE RESINS; INTRINSIC MICROPOROSITY; ADSORPTION; SORPTION; HG(II); XPS; CONDENSATION; FRAMEWORKS;
D O I
10.1016/j.polymer.2010.10.052
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Based on a facile catalyst-free process using Schiff base chemistry, here, highly cross-linked porous aminal networks in high yields (up to 90%) were rapidly prepared via microwave irradiation. The polymer networks contained as high as 50 wt% of nitrogen (N), in situ doped with sulfur (S), with specific surface areas of up to 301 m(2) g(-1), and were also found to exhibit a solvent-based luminescence property. Adsorption kinetics and isotherm studies demonstrated that the Hg2+ removal by these polymers was extremely rapid (90% being attained within 5 min for a 400 mg L-1 Hg2+ solution) and highly efficient (up to 1172 mg g(-1)). Particularly these materials also exhibited an excellent selectivity towards Hg2+ over other interfering ions (Cd2+, Ni2+, Zn2+, Cu2+, Co2+, Ca2+, Mn2+ and Mg2+). Studies by FT-IR, Raman and XPS spectra showed that all the N-containing groups (triazine ring, primary amine, and secondary amine) as well as S-containing groups on the polymer matrix could be responsible for the Hg adsorption, through the mechanism of surface complexation. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6193 / 6202
页数:10
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