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Tungsten sulfide highly boosted Fe(III)/peroxymonosulfate system for rapid degradation of cyclohexanecarboxylic acid: Performance, mechanisms, and applications.

Authors :
Lv, Xin
Li, Dazhen
Yu, Xi
McPhedran, Kerry N.
Huang, Rongfu
Source :
Chemosphere. Aug2024, Vol. 361, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

In this study, the Fe(III)/WS 2 /peroxymonosulfate (PMS) system was found to remove up to 97% of cyclohexanecarboxylic acid (CHA) within 10 min. CHA is a model compound for naphthenic acids (NAs), which are prevalent in petroleum industrial wastewater. The addition of WS 2 effectively activated the Fe(III)/PMS system, significantly enhancing its ability to produce reactive oxidative species (ROS) for the oxidation of CHA. Further experimental results and characterization analyses demonstrated that the metallic element W(IV) in WS 2 could provide electrons for the direct reduction of Fe(III) to Fe(II), thus rapidly activating PMS and initiating a chain redox process to produce ROS (SO 4 •−, •OH, and 1O 2). Repeated tests and practical exploratory experiments indicated that WS 2 exhibited excellent catalytic performance, reusability and anti-interference capacity, achieving efficient degradation of commercial NAs mixtures. Therefore, applying WS 2 to catalyze the Fe(III)/PMS system can overcome speed limitations and facilitate simple, economical engineering applications. [Display omitted] • Fe(III)/WS 2 /PMS system can achieve 97% removel rate of CHA within 10 min. • •OH, SO 4 •−, and 1O 2 are main ROS in the Fe(III)/WS 2 /PMS system. • W(IV) contained in WS 2 can promoting Fe(III)/Fe(II) cycle by providing electrons. • Fe(III)/WS 2 /PMS system can achieve efficient degradation of commercial NAs. • Fe(III)/WS 2 /PMS system exhibits excellent reusability and anti-interference. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
361
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
177907428
Full Text :
https://doi.org/10.1016/j.chemosphere.2024.142556