Efficient removal of uranium using a melamineitrimesic acid-modified hydrothermal carbon-based supramolecular organic framework

被引:43
|
作者
Li, Hualun [1 ]
Li, Ye [1 ]
Zhou, Yuzhi [1 ]
Li, Bolin [1 ]
Liu, Dongbin [1 ]
Liao, Hanyang [1 ]
机构
[1] Wuhan Univ Technol, Sch Resources & Environm Engn, Wuhan 430070, Hubei, Peoples R China
关键词
Uranium; Hydrothermal carbon; Supramolecular organic framework; Melamine; Trimesic acid; Adsorption; FUNCTIONALIZED MESOPOROUS SILICA; GRAPHENE OXIDE; AQUEOUS-SOLUTIONS; HIGH-PERFORMANCE; U(VI) REMOVAL; ADSORPTION; SORPTION; SURFACE; SEPARATION; RECOVERY;
D O I
10.1016/j.jcis.2019.02.079
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we prepared a hydrothermal carbon-based supramolecular organic framework (HTC-MA-TMA) by grafting melamine and trimesic acid on hydrothermal carbon (HTC) for efficient removal of U (VI) from aqueous solutions. The nano-sized supramolecular organic framework (SOF) particles consisted of N-donor-containing melamine and O-donor-containing trimesic acid self-assembled through hydrogen bonds. Their large number of specific active sites acted as the immobilization center for capturing U (VI). Chemical modification facilitated the dispersion of the SOF particles on HTC, which was synthesized using a novel covalent/non-covalent bond strategy. The HTC-MA-TMA adsorbent exhibited exceptional U (VI) adsorption capacity (271.83 mg/g) because of the coordination interaction between UO22+ and its ligands (amino, carboxyl and amide groups). The adsorption equilibrium was achieved within 30 min and followed a pseudo-second-order equation, suggesting the occurrence of a chemical adsorption process. Furthermore, the U (VI) ions adsorbed onto the HTC-MA-TMA adsorbent could be easily desorbed using 0.1 M HNO3 solution. This regeneration caused no significant decrease in the sorption capacity of the adsorbent. These results suggest that advanced HTC-MA-TMA adsorbent can be applied in the nuclear-fuel industry for extracting U (VI) from radioactive wastewater. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:14 / 24
页数:11
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