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Efficient Removal of U(VI) Using Functionalized Hollow Mesoporous Silica Nanospheres

机译:使用功能化的空心介孔二氧化硅纳米球有效去除U(VI)

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The capture and recycle uranium from wastewater is very important for the environmental protection and sustainable nuclear energy development. In this work, functionalized hollow mesoporous silica nanospheres bearing aminopropyl and Schiff base groups, abbreviated as HMSNs-NH2 and HMSNs-SA, respectively, were prepared for the removal of U(VI) from aqueous solution. The effects of solution pH, adsorption kinetics, thermodynamics and isotherms, as well as the presence of competing metal ions on the uranium adsorption onto the two adsorbents were investigated in detail. It was found that both adsorbents showed largely enhanced adsorp- tion capacity and good selectivity towards U(VI) than unfunc- tionalized HMSNs. The maximum adsorption capacities reach 499.72 mg/g for HMSNs-NH2 and 317.29 mg/g for HMSNs-SA, which are at a high level compared with the reported functionalized mesoporous silica materials. Furthermore, both adsorbents can rapidly remove uranium with the removal rate more than 97% from tap water and 85% from seawater with injected uranium of 5 ppm. The findings of the present work provide new actinide adsorbents by combining organic ligands with hollow mesoporous matrixes.
机译:废水的捕获和回收铀对环境保护和可持续核能发展非常重要。在这项工作中,分别为HMSNS-NH2和HMSNS-SA缩写为带有氨基丙基和Schiff碱基的功能化的空心介孔二氧化硅纳米球,以从水溶液中去除U(VI)。详细研究了溶液pH值,吸附动力学,热力学和等温线,以及竞争金属离子对铀吸附在两个吸附剂上的影响。发现两个吸附剂在很大程度上都表现出对U(VI)的吸附能力和良好的选择性,而不是未经置换的HMSN。 HMSNS-NH2的最大吸附能力达到499.72 mg/g和HMSNS-SA的317.29 mg/g,与报道的功能化介孔二氧化硅材料相比,它们的水平很高。此外,两种吸附剂都可以从自来水中的去除率迅速去除铀,从自来水中的97%和85%的海水注射了5 ppm。本工作的发现通过将有机配体与空心介孔矩阵相结合,从而为新的actacinide吸附剂提供了新的吸附剂。

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