Degradation of phosphonates in Co(II)/peroxymonosulfate process: Performance and mechanism

Abstract

The increased release of phosphonates to natural waters causes global concern due to their potential threat to the aquatic environment. It is curial to mineralize phosphonates to orthophosphate (PO43–) before they are thoroughly removed from wastewater via conventional biological treatment. In this study, we systematically investigated the performance and mechanism of degradation of phosphonates in Co(II)-triggered peroxymonosulfate (PMS) activation process. The degradation efficiency of various phosphonates is highly dependent on their coordination with Co(II). Using 1-hydroxyethane 1,1-diphosphonic acid (HEDP) as a target pollutant, the Co(II)/PMS process is effective in a broad solution pH range from 5.0 to 10.0. Multiple experimental results imply that Co(II)-PMS complex is the primary reactive species, while hydroxyl radicals (HO•), sulfate radicals (SO4•−), singlet oxygen (1O2) and Co(III) play as the secondary reactive species for the degradation of HEDP. The presence of Cl–, HCO3–, and natural organic matters (NOM) inhibits the degradation of HEDP. However, in real water samples, the selectivity and efficiency for HEDP removal in the Co(II)/PMS process are higher than that in free radicals-mediated advanced oxidation processes. This study not only sheds new lights on the mechanism of Co(II)-triggered PMS activation process, but also provides feasible technology for the degradation of phosphonates in wastewater.