Highly efficient enrichment mechanism of U(VI) and Eu(III) by covalent organic frameworks with intramolecular hydrogen-bonding from solutions

被引:135
作者
Zhong, Xin [1 ]
Liang, Wen [1 ]
Lu, Zhipeng [1 ]
Hu, Baowei [1 ]
机构
[1] Shaoxing Univ, Sch Life Sci, Huancheng West Rd 508, Shaoxing 312000, Peoples R China
关键词
COF; TpPa-1; U(VI); Eu(III); Adsorption; H-bonding; AQUEOUS-SOLUTIONS; ADSORPTION; CONSTRUCTION; URANIUM; MICROSPHERES; REMOVAL; SORPTION;
D O I
10.1016/j.apsusc.2019.144403
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 investigation, TpPa-1 were synthesized and exploited for radionuclides ions elimination. According to Langmuir model, at pH 6.5 and 298 K, the maximum adsorption quantity of TpPa-1 were 1194.07 mg(U(VI))/g and 1107.63 mg(Eu(III))/g, respectively. The superior adsorption performance could be attributed to: (i) a great quantity of heteroatom activated sites on the pore wall could conduct as cation receptors; (ii) the forming intramolecular -C=(NHO)-H-center dot center dot center dot-O-center dot center dot center dot= hydrogen bonding in the network of TpPa-1, which was U(VI) and Eu(III) ions adsorption sites; (iii) hydrogen bonding could adjust the electron density of the complex and abate the total charge of radionuclides. The outcomes of this work suggest that TpPa-1 is a promising adsorbent, which is appropriate to enrichment and separation radionuclides from polluted wastewater.
引用
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页数:13
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