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Low-temperature plasma induced phosphate groups onto coffee residue-derived porous carbon for efficient U(Ⅵ) extraction    

文献类型:期刊文献

中文题名:Low-temperature plasma induced phosphate groups onto coffee residue-derived porous carbon for efficient U(Ⅵ) extraction

作者:Zhongshan Chen[1,2];Xuan He[2];Qian Li[2];Hui Yang[2];Yang Liu[2];Lining Wu[3];Zhixin Liu[1];Baowei Hu[1];Xiangke Wang[1,2]

机构:[1]School of Life Science,Shaoxing University,Shaoxing 312000,China;[2]College of Environmental Science and Engineering,North China Electric Power University,Beijing 102206,China;[3]School of Energy Power and Mechanical Engineering,North China Electric Power University,Beijing 102206,Chin

年份:2022

卷号:34

期号:12

起止页码:1

中文期刊名:环境科学学报:英文版

外文期刊名:Journal of Environmental Sciences

收录:CSTPCD、、CSCD2021_2022、Scopus、CSCD、PubMed

基金:supported by the National Key Research and Development Program of China(Nos.2018YFC1900105,2016YFA0203200,2017YFA0207002);the Beijing Outstanding Young Scientist Program and the Fundamental Research Funds for the Central Universities(No.2019MS044)。

语种:英文

中文关键词:U(Ⅵ);Coffee residue;Porous carbon;Low-temperature plasma;modification

中文摘要:For the continuous utilization of nuclear energy and efficient control of radioactive pollution, low-cost materials with high efficient U(VI) removal are of great importance. In this study, low temperature plasma method was applied for the successful modification of Ophosphorylethanolamine(O-PEA) on the porous carbon materials. The produced materials(Cafe/O-PEA) could adsorb U(VI) efficiently with the maximum sorption capacity of 648.54mg/g at 1 hr, T=298 K, and p H=6.0, much higher than those of most carbon-based composites. U(VI) sorption was mainly controlled by strong surface complexation. From FTIR,SEM-EDS and XPS analyses, the sorption of U(VI) was related to the complexation with-NH2, phosphate and-OH groups on Cafe/O-PEA. The low temperature plasma method was an efficient, environmentally friendly and low-cost method for surface modification of materials for the effective enrichment of U(VI) from aqueous solutions.

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