Photo-assisted degradation of 2,4,5-trichlorophenoxyacetic acid by Fe(II)-catalyzed activation of Oxone process: The role of UV irradiation, reaction mechanism and mineralization

Y. R. Wang, Wei Chu

Research output: Journal article publicationJournal articleAcademic researchpeer-review

64 Citations (Scopus)

Abstract

In this study, the potential of Fe(II)-catalyzed activation of Oxone process with UV irradiation (FOU) for the degradation of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) in aqueous solution was explored and compared with the Fe(II)/Oxone (FO) process. Experimental results show that the FO process was dramatically promoted upon the introduction of UV irradiation. As a result, the role of UV irradiation was elucidated in-depth by comparing the real-time of [Fe(II)] between the FO process and the FOU process. It was found that a beneficial Fe(III)/Fe(II) catalytic cycle is established in the presence of UV irradiation, thereby leading to the accelerated regeneration of Fe(II). Additionally, 2,4,5-T decay by the FOU process under various [Oxone] and [2,4,5-T] was also examined. Furthermore, the decay pathways for the transformation of 2,4,5-T by UV alone, Oxone/UV, and FOU processes were proposed by using LC-ESI/MS analysis. Distinct differences of intermediate distributions were observed among the three processes with or without the involvement of radicals (OH and SO4-). Besides, the efficiencies of various processes (i.e., UV alone, Oxone/UV and FOU) were further examined in terms of mineralization and Cl-ion accumulation.
Original languageEnglish
Pages (from-to)151-161
Number of pages11
JournalApplied Catalysis B: Environmental
Volume123-124
DOIs
Publication statusPublished - 23 Jul 2012

Keywords

  • 2,4,5-Trichlorophenoxyacetic acid
  • Hydroxyl radical
  • Oxone
  • Sulfate radical
  • UV irradiation

ASJC Scopus subject areas

  • Catalysis
  • Environmental Science(all)
  • Process Chemistry and Technology

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