中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis and characterization of novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials for effective separation of cesium

文献类型:期刊论文

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作者Xiao, CL; Zhang, AY; 柴之芳;Chai, ZF
刊名JOURNAL OF HAZARDOUS MATERIALS ; JOURNAL OF HAZARDOUS MATERIALS
出版日期2014 ; 2014
卷号267页码:109-118
关键词Calix[4]arene-crown Macroporous silica Cesium Adsorption Separation Calix[4]arene-crown Macroporous silica Cesium Adsorption Separation
ISSN号0304-3894
DOI10.1016/j.jhazmat.2013.12.048
英文摘要Two novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials, 25,27-bis(n-octyloxy)calix[4]arene-crown-6 (BnOCalix[4]C6)/SiO2-P and 25,27-bis(i-octyloxy)calix[4]arene-crown-6 (BiOCalix[4]C6)/SiO2-P were synthesized by in situ polymerization and impregnation techniques. The obtained materials were characterized by scanning electron microscope (SEM), particle size distribution, nitrogen adsorption-desorption isotherms, thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR) spectroscopy, Si-29 solid-state NMR, and powder X-ray diffraction (XRD). The adsorption of some typical fission and non-fission products Na(I), K(I), Rb(I), Cs(I), Sr(II), Ba(II), La(III), Y(III), Pd(II), Ru(III), Zr(IV), and Mo(VI) onto BnOCalix[4]C6/SiO2-P and BiOCalix[4]C6/SiO2-P in HNO3 solution was investigated. The bleeding of the materials in HNO3 solution was evaluated by analysis of total organic carbon (TOC). BnOCalix[4]C6/SiO2-P and BiOCalix[4]C6/SiO2-P exhibited excellent adsorption ability and high selectivity for Cs(I) over all the other tested metals. Crown Copyright (C) 2013 Published by Elsevier B.V. All rights reserved.; Two novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials, 25,27-bis(n-octyloxy)calix[4]arene-crown-6 (BnOCalix[4]C6)/SiO2-P and 25,27-bis(i-octyloxy)calix[4]arene-crown-6 (BiOCalix[4]C6)/SiO2-P were synthesized by in situ polymerization and impregnation techniques. The obtained materials were characterized by scanning electron microscope (SEM), particle size distribution, nitrogen adsorption-desorption isotherms, thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR) spectroscopy, Si-29 solid-state NMR, and powder X-ray diffraction (XRD). The adsorption of some typical fission and non-fission products Na(I), K(I), Rb(I), Cs(I), Sr(II), Ba(II), La(III), Y(III), Pd(II), Ru(III), Zr(IV), and Mo(VI) onto BnOCalix[4]C6/SiO2-P and BiOCalix[4]C6/SiO2-P in HNO3 solution was investigated. The bleeding of the materials in HNO3 solution was evaluated by analysis of total organic carbon (TOC). BnOCalix[4]C6/SiO2-P and BiOCalix[4]C6/SiO2-P exhibited excellent adsorption ability and high selectivity for Cs(I) over all the other tested metals. Crown Copyright (C) 2013 Published by Elsevier B.V. All rights reserved.
学科主题Engineering; Environmental Sciences & Ecology ; Engineering; Environmental Sciences & Ecology
收录类别SCI
电子版国际标准刊号1873-3336
语种英语
WOS记录号WOS:000332812500014 ; WOS:000332812500014
公开日期2016-05-03
源URL[http://ir.ihep.ac.cn/handle/311005/225084]  
专题高能物理研究所_院士
推荐引用方式
GB/T 7714
Xiao, CL,Zhang, AY,柴之芳;Chai, ZF. Synthesis and characterization of novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials for effective separation of cesium, Synthesis and characterization of novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials for effective separation of cesium[J]. JOURNAL OF HAZARDOUS MATERIALS, JOURNAL OF HAZARDOUS MATERIALS,2014, 2014,267, 267:109-118, 109-118.
APA Xiao, CL,Zhang, AY,&柴之芳;Chai, ZF.(2014).Synthesis and characterization of novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials for effective separation of cesium.JOURNAL OF HAZARDOUS MATERIALS,267,109-118.
MLA Xiao, CL,et al."Synthesis and characterization of novel macroporous silica-polymer-calixcrown hybrid supramolecular recognition materials for effective separation of cesium".JOURNAL OF HAZARDOUS MATERIALS 267(2014):109-118.

入库方式: OAI收割

来源:高能物理研究所

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