4.7 Article

Octadecylamine degradation through catalytic activation of peroxymonosulfate by Fe-Mn layered double hydroxide

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 695, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2019.133963

Keywords

PMS; Fe-Mn-LDH; Octadecylamine

Funding

  1. National Natural Science Foundation of China [51978319]
  2. National College student innovation and Entrepreneurship training program of Lanzhou University
  3. Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources, Qinghai Institute of Salt Lake, Chinese Academy of Sciences

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A kind of heterogeneous catalyst, Fe-Mn layered double hydroxide (Fe-Mn-LDH), was fabricated by coprecipitation process and used as PMS activator to degrade a novel organic pollutant octadccylamine (ODA). And the X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microcopy (TEM), Mapping and X-ray photoelectron spectra (XPS) measurements were utilized to characterize the fresh and used Fe-Mn-LDH. After a serious of degradation experiments, it was clearly to see that the activator possessed excellent activation property for PMS and was capable of removing 85% ODA (10 mg. L-1) within 25 min obviously higher than pure PMS. Moreover, the effect of some elements (such as PMS consumption, catalyst consistence and initial pH value), different reaction system and catalyst repeatability on ODA degradation were also explored. And by identification of main radical experiment, SO4. and HO center dot were both confirmed the primaly radicals. What's more, extra anion and nature organic matter (NOM) addition experiment displayed that NOM, NO3 and COi perform a negative effect on ODA degradation but Cl could promote it. In addition, repeated experiments and metal leaching after degradation showed good stability of Fe-Mn-LDH. Finally, based on the XPS and Gas Chromatography-Mass Spectrometer (GS-MS) technology, the possible degradation mechanism and pathway were proposed. (C) 2019 Elsevier B.V. All rights reserved.

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