4.7 Article

Preparation of molecularly imprinted ordered mesoporous silica for rapid and selective separation of trace bisphenol A from water samples

期刊

APPLIED SURFACE SCIENCE
卷 448, 期 -, 页码 380-388

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2018.04.017

关键词

Ordered mesoporous silica; Surface molecularly imprinted; Selective separation; Bisphenol A; Water samples

资金

  1. NSFC [21677060, 51402126, 51503079]
  2. Program for Science and Technology of Zhejiang Province [2015C32067, 2018C37076, 2018C37075, LGF18B060005, LGF18B050004]
  3. Natural Science Foundation of Zhejiang Province [LY16B050007, Y18B050014]

向作者/读者索取更多资源

A novel molecularly imprinted ordered mesoporous silica SBA-15 (MI-SBA-15) was prepared using a semi-covalent approach to achieve high selectivity toward bisphenol A (BPA) from water samples. The structure and morphology of synthesized MI-SBA-15 were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, thermogravimetry, X-ray diffraction, and N-2 absorption analysis. Results show that MI-SBA-15 possessed highly ordered mesoporous structure with large surface area. Batch experiments were conducted to investigate the rebinding capability of MI-SBA-15 to BPA, showing rapid kinetics, high rebinding capacity, and excellent selectivity. The experimental data fitted well to the pseudo-second-order model and Langmuir-Freundlich adsorption isotherm, indicating chemical adsorption as the rate-limiting step. In addition, selectivity assay showed all the relative selectivity coefficients toward BPA over its structure analogs, which were higher than 132, further indicating the significant enhancement of the rebinding selectivity of MI-SBA-15. Furthermore, water samples were analyzed with MI-SBA-15 successfully, showing high recovery in the range of 87.0%-110.2%. In conclusion, MI-SBA-15 possessed high affinity and selectivity and compelling adsorption capacity for the extraction of BPA from water samples. (C) 2018 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据