AI Article Synopsis

  • Peroxyacids (POAs) like performic acid, peracetic acid, and perpropionic acid are studied as alternatives to chlorine for reducing harmful byproducts in water disinfection.
  • The study found that POAs were more effective than chlorine at inactivating certain bacteria, but less effective at inactivating viruses, indicating selective interactions with specific biomolecules.
  • Understanding how POAs interact with bacteria and viruses could help improve their use in water and wastewater treatment processes.

Article Abstract

Peroxyacids (POAs) are a promising alternative to chlorine for reducing the formation of disinfection byproducts. However, their capacity for microbial inactivation and mechanisms of action require further investigation. We evaluated the efficacy of three POAs (performic acid (PFA), peracetic acid (PAA), and perpropionic acid (PPA)) and chlor(am)ine for inactivation of four representative microorganisms ( (Gram-negative bacteria), (Gram-positive bacteria), MS2 bacteriophage (nonenveloped virus), and Φ6 (enveloped virus)) and for reaction rates with biomolecules (amino acids and nucleotides). Bacterial inactivation efficacy (in anaerobic membrane bioreactor (AnMBR) effluent) followed the order of PFA > chlorine > PAA ≈ PPA. Fluorescence microscopic analysis indicated that free chlorine induced surface damage and cell lysis rapidly, whereas POAs led to intracellular oxidative stress through penetrating the intact cell membrane. However, POAs (50 μM) were less effective than chlorine at inactivating viruses, achieving only ∼1-log PFU removal for MS2 and Φ6 after 30 min of reaction in phosphate buffer without genome damage. Results suggest that POAs' unique interaction with bacteria and ineffective viral inactivation could be attributed to their selectivity toward cysteine and methionine through oxygen-transfer reactions and limited reactivity for other biomolecules. These mechanistic insights could inform the application of POAs in water and wastewater treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690719PMC
http://dx.doi.org/10.1021/acs.est.2c09824DOI Listing

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