Peracetic Acid Activation by Modified Hematite for Water Purification: Performance, Degradation Pathways, and Mechanism.

Langmuir

Engineering Research Center of Eco-Environment in Three Gorges Reservoir Region of Ministry of Education, College of Hydraulic & Environmental Engineering, College of Materials and Chemical Engineering, China Three Gorges University, Yichang, Hubei 443002, China.

Published: July 2024

AI Article Synopsis

  • Natural mineral-based advanced oxidation processes (AOPs) are gaining popularity for effectively breaking down pollutants, with this study focusing on modifying Hematite to enhance its capabilities.
  • The modified Hematite (Hematite-(R)) demonstrated a 21.7% increase in the degradation rate of cefazolin (CFZ) when activated with peracetic acid (PAA) compared to regular Hematite.
  • The research identified key reactive species involved in the CFZ removal process and revealed that Hematite-(R) is effective across a wide pH range, with its performance impacted by certain ions and humic acid concentrations.

Article Abstract

Natural mineral-based advanced oxidation processes (AOPs) are now receiving increasing attention for the efficient degradation of pollutants. In this work, we used a common reducing agent (NaBH) to treat natural Hematite to obtain modified Hematite (Hematite-(R)) and applied it to activate peracetic acid (PAA) for efficient degradation of cefazolin (CFZ). Compared with Hematite, the Hematite-(R)/PAA system increased the degradation rate of CFZ by 21.7% within 80 min under neutral conditions. Scavenging experiments and electron paramagnetic resonance (EPR) technology were introduced to identify the principal roles of O, CHC(O)OO, and OH for CFZ removal over the Hematite-(R)/PAA process. The outstanding capability of Hematite-(R) could be mainly due to the higher percentage of Fe(II) (52%) on the surface of catalysts. Furthermore, the possible degradation pathways of CFZ were explored. Moreover, the Hematite-(R)/PAA process showed a superior CFZ removal efficiency with a wide initial pH scope of 1.0-9.0. The degradation efficiency of CFZ showed a negligible effect in the presence of Cl, SO, and NO, while significant inhibition was recorded after the addition of HPO and CO. The inhibition of humic acid (HA) on CFZ degradation via the Hematite-(R)/PAA process showed an obvious concentration dependence. This work could provide strong support for the use of natural Hematite in water purification.

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Source
http://dx.doi.org/10.1021/acs.langmuir.4c01969DOI Listing

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