Literature DB >> 34736182

Targeted degradation of TBBPA using novel molecularly imprinted polymer encapsulated C-Fe-Nx nanocomposite driven from MOFs.

Cheng Zeng1, Yan Wang2, Tong Xiao1, Zhicheng Yan1, Jinquan Wan3, Quanmo Xie1.   

Abstract

To improve the efficacy of organic pollutant removal using sulfate radicals, we designed MIP@C-Fe-Nx, a molecularly imprinted material capable of targeting the degradation of tetrabromobisphenol A (TBBPA), which can be used as both adsorbent and catalyst to recognize and degrade Tetrabromobisphenol A (TBBPA) accurately, and the final removal rate of TBBPA can reach 104.6 mg·g-1. Based on the synergistic effects of MIP@C-Fe-Nx on the excellent organic pollutant recognition and catalytic performance, low concentrations of TBBPA can be pre-targeted, concentrated, and fixed on the surface of MIP, and degraded simultaneously in-situ by·OH and SO4•- which are produced by activating PS with C-Fe-Nx. Recognition experiments demonstrated that MIPs had perfect performance in recognizing and adsorbing TBBPA and debromination intermediates. The DFT calculations and HPLC-MS analysis indicated that MIP@C-Fe-Nx had a targeted recognition and accumulation for TBBPA and debromination intermediates, for example, dibromobisphenol A, monobromobisphenol A, and bisphenol A, thus avoid the formation of toxic intermediates causing secondary contamination.
Copyright © 2021 Elsevier B.V. All rights reserved.

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Keywords:  N-doped carbon-encapsulated Fesurface molecular imprinting; advanced oxidation technology; synergetic effect; tetrabromobisphenol A

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Year:  2021        PMID: 34736182     DOI: 10.1016/j.jhazmat.2021.127499

Source DB:  PubMed          Journal:  J Hazard Mater        ISSN: 0304-3894            Impact factor:   10.588


  1 in total

1.  Magnetic Surface Molecularly Imprinted Polymer for Selective Adsorption of 4-Hydroxycoumarin.

Authors:  Yi Kuang; Yunlong Xia; Xing Wang; Qingqing Rao; Shengxiang Yang
Journal:  Front Chem       Date:  2022-04-07       Impact factor: 5.545

  1 in total

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