4.7 Article

Perdisulfate-assisted advanced oxidation of 2,4-dichlorophenol by bio-inspired iron encapsulated biochar catalyst

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 592, Issue -, Pages 358-370

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.02.056

Keywords

Bio-inspired catalyst; Fe?BC; Micro-electrolysis; 2; 4-dichlorophenol removal; Advanced oxidation processes

Funding

  1. National Natural Science Foundation of China [51908375]
  2. Guangxi innovation research team project [2018GXNSFGA281001]
  3. National Key Research and Development Program [2019YFC0408602, 2019YFC1906704]
  4. Guangxi Key Laboratory of Theory and Technology for Environmental Pollution Control [1901K001]
  5. Tianjin Natural Science Foundation [18JCQNJC77300]

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In order to enhance advanced oxidation processes (AOPs), bio-inspired iron-encapsulated biochar (bio-inspired Fe?BC) catalysts were prepared from iron-rich biomass of Iris sibirica L. The high performance of micro-electrolysis in degrading 2,4-DCP was attributed to the formation of Fe and austenite with strong electron carrier at 700 ?C.
To improve advanced oxidation processes (AOPs), bio-inspired iron-encapsulated biochar (bio-inspired Fe?BC) catalysts with superior performance were prepared from iron-rich biomass of Iris sibirica L. using a pyrolysis method under anaerobic condition. The obtained compounds were used as catalysts to activate perdisulfate (PDS) and then degradate 2,4-dichlorophenol (2,4-DCP), and synthetic iron-laden biochar (synthetic Fe-BC) was used for comparison. The highest removal rate of 2,4-DCP was 98.35%, with 37.03% of this being distinguished as the contribution of micro-electrolysis, greater than the contribution of adsorption (32.81%) or advanced oxidation (28.51%). The high performance of micro-electrolysis could be attributable to the formation of Fe (Iron, syn) and austenite (CFe15.1) with strong electron carrier at 700 ?C. During micro-electrolysis, Fe2+ and electrons were gradually released and then used as essential active components to enhance the AOPs. The slow-releasing Fe2+ (K = 0.0048) also inhibited the overconsumption of PDS (K = -0.00056). Furthermore, the electrons donated from Fe?BC-4 were able to activate PDS directly. The electrons were enriched by the porous structure of Fe?BC-4, and the formation of the -C-O-Fe bond in the p-electron system could also accelerate the electron transfer to activate PDS. Similar reactive oxygen species (ROS) were identified during the micro-electrolysis and AOPs, leading to similar degradation pathways. The higher does concentration of center dot O2? generated during micro-electrolysis than during the AOPs also led to a greater dechlorination effect. (c) 2021 Elsevier Inc. All rights reserved.

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