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Highly efficient enrichment mechanism of U(VI) and Eu(III) by covalent organic frameworks with intramolecular hydrogen-bonding from solutions  ( SCI-EXPANDED收录 EI收录)   被引量:115

文献类型:期刊文献

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

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

年份:2020

卷号:504

外文期刊名:APPLIED SURFACE SCIENCE

收录:SCI-EXPANDED(收录号:WOS:000502040600134)、、EI(收录号:20194807742163)、Scopus(收录号:2-s2.0-85075457820)、WOS

基金:Financial support from the Research Fund Program of National Nature Science Foundation of China (No. 21876115).

语种:英文

外文关键词:COF; TpPa-1; U(VI); Eu(III); Adsorption; H-bonding

外文摘要: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.

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