吸附
化学工程
嫁接
材料科学
铀酰
纳米纤维
水溶液
聚合
聚乙烯醇
萃取(化学)
海水
高分子化学
铀
化学
纳米技术
色谱法
有机化学
复合材料
聚合物
海洋学
地质学
工程类
冶金
作者
Chen Huang,Mengtao Fu,Lin Ma,Chengkai Mao,Yunyou Yao,Ling Xu,Lu Xu,Jiaguang Han,Xiaogang Xue,Gang Xu,Minghong Wu,Haiyang Shao,Hongjuan Ma
标识
DOI:10.1016/j.cej.2023.145718
摘要
Application of amidoxime (AO) based fibrous adsorbents in uranium extraction from seawater (UES) is hampered in their adsorption performance and preparation process, including two items: firstly, low grafting kinetics of monomer acrylonitrile (AN) and large amount of its homopolymers, secondly, low extraction efficiency limiting by the ultralow concentration of uranium and temperature of seawater. Herein, an ultrafast strategy to prepare AO based nanofibers (NFs) with polyvinyl alcohol (PVA) super hydrophilic slit nanopore structure via radiation crosslinking and grafting polymerization (c-PVA-g-PAO NFs) was designed. Combined with hydrophilic 2D MXene nanosheets for excellent photothermal and photoelectric synergistic assistance, further improved the adsorption performance of the material (c-PVA-g-PAO&MXene NFs). Super hydrophilic PVA NFs with water-resistant three-dimensional network structure generated by radiation crosslinking realized ultrafast graft polymerization of AN. Within 1 min AN can be grafted throughout the c-PVA NFs in its aqueous solution with degree of grafting (DG) 73.71%, and construct a well-developed slit nanopore structure inside and outside of the fiber. Through ultrasound, MXene can be effectively loaded on the surface of the nanofiber, and further enhance 30.16% of the adsorption capacity of the material under light with MXene content 8 wt%. The c-PVA-g-PAO&MXene NFs achieved adsorption capacity of uranium with 2.23 mg/g in natural seawater for 1 week, which increased 26.70% than in dark (1.76 mg/g). And it could undergo at least 5 cycles of adsorption and elution. This novel strategy with ultrafast grafting, facile operating process and solar-induced synergy provided a new ideal to promote the industrialization process of UES.
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