The development of oxidation processes with generating powerful radicals is the most interesting and thought-provoking dimension of peroxymonosulfate (PMS) activation. In this study, a magnetic spinel CuFe2O4 was successfully prepared by a facile, non-toxic, cost-efficient co-precipitation method with the synergetic effect of photocatalytic PMS oxidation against recalcitrant benzotriazole (BTA) pollutant. The high particle dispersion and large surface area (201.898 m2/g) provided a high photocatalytic activity with CuFe2O4. The obtained results from the central composite design (CCD) analysis confirmed the optimum degrading rate of BTA reached 81.4% at the optimum operational condition of CuFe2O4= 0.4 g/L, PMS= 2 mM, BTA= 20 mg/L after 70 min irradiation time. As such, the active species capture experiments revealed the presence of •OH, SO4•‒, O2•‒ and h+ species in CuFe2O4/UV/PMS system where SO4•‒ was dominated for BTA photodegradation. The combination of photocatalysis and PMS activation enhanced the consumption of metal ions in redox cycle reactions, thus preventing metal leaching and maintain the recyclability with reasonable mineralization efficiency which achieved more than 40% total organic carbon removal after four batch experiments. A retardant effect on BTA oxidation was observed with comparing the water’s common anion constituents as HCO3‒ > Cl‒ > NO3‒ > SO2‒. Results from intermediates identification showed that the transformation pathway of BTA developed as the deprotonation, hydrolysis and ring cleavage processes promoting the practical potential of photo-absorbing CuFe2O4 catalyzed PMS which can be a promising method due to convenient magnetic separation form the solution.

The study evaluated potassium peroxymonosulfate (PPMS) efficacy against rifampicin-resistant Salmonella Infantis (rif-SI), Escherichia coli (E. coli), Salmonella Infantis (SI), Newcastle disease virus (NDV) and avian influenza virus (AIV). The assessment encompassed varied concentrations, organic material conditions, and exposure durations to comprehensively evaluate PPMS efficacy. Moreover, PPMS’s efficacy was tested on diverse carrier surfaces and clothing to evaluate its bactericidal and virucidal potential. At the recommended concentrations (1X), PPMS effectively inactivated all pathogens within 5 sec, except for NDV, which required 30 sec in the presence of organic materials. At 0.5X, PPMS successfully inactivated E. coli, AIV and NDV within 5 sec in the absence of organic material. However, rif-SI and SI necessitated 30 sec for inactivation. Most pathogens were inactivated within 30 sec, with the exception for AIV, which was inactivated within 5 sec. PPMS effectively eliminated rif-SI on all carriers within 30 sec. Moreover, at both concentrations, PPMS successfully inactivated AIV on all carriers within 30 sec, except on stainless steel at 0.5X. Furthermore, PPMS at both concentrations required 5 and 30 sec, respectively, to inactivate AIV on the rayon sheet. Therefore, due to its demonstrated efficacy against a wide range of pathogens across diverse surfaces, PPMS emerges as a crucial alternative disinfectant significantly enhancing biosecurity on and around chicken farms. found in and around animal farms, slaughterhouses, and hospitals.

Azo dyes are the most widely used synthetic dyes in the printing and dyeing process. However, the discharge of untreated azo dyes poses potential threat for human health and aqueous ecosystem. Herein, we fabricated a novel heterogenous catalyst - activated carbon fiber-supported ferric alginate (FeAlg-ACF) . Together with peroxymonosulfate (PMS) and visible light, this photocatalytic oxidation system was used to remove an azo dye - azophloxine. The results indicated that the proposed catalytic oxidation system can remove 100% azophloxine within 24 min, while under the same system, the removal rate was only 92 % and 84 % when ferric alginate was replaced with ferric citrate and ferric oxalate respectively, which showed the superiority of activated carbon fiber-supported ferric alginate. The degradation of azophloxine is achieved by the active radicals (SO4•− and •OH) released from PMS and persistent free radicals from activated carbon fiber. After treating for 24 min, the total organic carbon of azophloxine solution (50 μmol/L) decreased from 1.82 mg/L to 79.3 μg/L and the nitrate concentration of ions increased from 0.3 mg/L to 8.6 mg/L. That is, up to 93.5% azophloxine molecules were completely degraded into inorganic compounds. Consequently, potential secondary contamination by intermediate organic products during catalytic degradation was prohibited. The azophloxine removal ratio was kept almost constant after seven cycles, indicating the recyclability and longevity of this system. Furthermore, the azophloxine removal was still promising at high concentrations of Cl-, HCO3-, CO32-. Therefore, our proposed system is potentially effective to remove dye pollutants from seawater. It provides a feasible method for the development of efficient and environmental friendly PMS activation technology combined with FeAlg-ACF, has significant academic and application value.