Cyclized polyacrylonitrile amidoxime with local conjugate domain for high-efficiency extraction of uranium from seawater

被引:50
作者
Xu, Yachao [1 ,2 ]
Yu, Jing [1 ,2 ]
Zhu, Jiahui [1 ,2 ]
Liu, Qi [1 ,2 ,3 ]
Zhang, Hongsen [1 ,2 ]
Liu, Jingyuan [1 ,2 ]
Chen, Rongrong [1 ,2 ]
Li, Ying [4 ]
Wang, Jun [1 ,2 ]
机构
[1] Harbin Engn Univ, Key Lab Superlight Mat & Surface Technol, Minist Educ, Harbin 150001, Peoples R China
[2] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Harbin 150001, Peoples R China
[3] Hainan Harbin Inst Technol Innovat Res Inst Co Ltd, Hainan 572427, Peoples R China
[4] Jilin Univ, Coll Chem, Lab Theoret & Computat Chem, Changchun 130023, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2022年 / 316卷
基金
中国博士后科学基金;
关键词
Photocatalysis; Electronic transmission; Polyacrylonitrile; Uranium; Amidoxime; MOLECULAR-DYNAMICS SIMULATIONS; AQUEOUS-SOLUTION; FUNCTIONALIZED GRAPHENE; URANYL-ION; ADSORPTION; COMPLEXES; STRATEGY; SURFACE; U(VI);
D O I
10.1016/j.apcatb.2022.121677
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
Polyacrylonitrile (PAN) has slow surface dynamics due to its low electron transport capacity, which greatly limits its application in the extraction of uranium (U(VI)) from seawater. Here, we propose a local conjugation domain (LCD) structure between adjacent microdomains of cyclized polyacrylonitrile (CPAN) with different conjugation structures. This structure uses the potential difference between different degrees of conjugate domains to form a built-in field that promotes charge separation. Cyclized polyacrylonitrile amideoxime (CPAO) formed by hydrolyzing the cyano groups that are not involved in conjugation in CPAN can better capture the U(VI) in seawater. After floating in marine for 30 days, the U(VI) extraction capacity of CPAO can reach 5.2 mg g-1, which is 3 times that of PAO. This LCD strategy can be extended to other conjugated high-molecular polymers, thereby it is proposed as a general method for rational design of efficient seawater U(VI) extraction materials.
引用
收藏
页数:9
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