4.7 Article

A dual-oxidant advanced oxidation process system containing CaO2 and peroxymonosulfate for organic pollutant degradation: High adaptability and synergistic effect

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 308, Issue -, Pages -

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ELSEVIER
DOI: 10.1016/j.seppur.2022.122909

Keywords

Peroxymonosulfate; Calcium peroxide; Tetracycline degradation; Non-radical advanced oxidation process

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A dual-oxidant advanced oxidation process (AOP) system comprising calcium peroxide (CaO2) and peroxymonosulfate (PMS) was developed for efficient degradation of refractory organic pollutants. The system showed high degradation efficiency of tetracycline (TC), following a pseudo second-order kinetic model, with 91% degradation achieved within 4 minutes at room temperature using 0.1 g/L CaO2 and 0.3 g/L PMS. The system exhibited strong anti-interference capabilities and was effective over a wide pH range (3-12) and for various organic pollutants.
In this study, a dual-oxidant advanced oxidation process (AOP) system containing calcium peroxide (CaO2) and peroxymonosulfate (PMS) was developed for the first time to efficiently degrade refractory organic pollutants. It was found that the system with 0.1 g/L CaO2 and 0.3 g/L PMS could degrade more than 91% of 50 mg/L tetracycline (TC) within 4 min at room temperature, and the degradation process much followed the pseudo second-order kinetic model. The presented AOP system exhibited strong anti-interference capabilities towards coexisting inorganic anions (Cl-, SO42-, NO3-, HCO3- and HPO42-) and humic acid (HA), even at high concentra-tions. Moreover, the system could efficiently work in a wide pH (3-12) range, suitable for natural waterbodies and various organic pollutants. The results of quenching experiments and electron paramagnetic resonance (EPR) tests demonstrated that singlet oxygen (1O2) was the dominate reactive oxygen species (ROS) responsible for organics degradation. A synergistic mechanism of the dual-oxidant system was confirmed by a series of comparative experiments, where CaO2 continuously provided OH- and H2O2, and then combined with PMS to produce predominant 1O2 and inferior O2 center dot-, respectively. Further, the possible pathways of TC degradation were deduced based on analyses of the intermediates.

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