摘要
Advanced oxidation process is powerful for removal of tetracycline (TC) from wastewater by the catalytic peroxymonosulfate (PMS) activation. It is a key to full dispersion and confinement of active centers in the catalytic system. Herein, the active Cu species were supported into mesoporous SiO 2 , which was used to activate PMS for removal of TC. Reduction temperatures revealed that the vast majority of CuO can be reduced to Cu 2 O and Cu species at 300 °C under H 2 /Ar, which offered the best performance for TC removal efficiency of 97.1 %. Noteworthily, CuO 1-x /SiO 2 -300 displayed a better activity than CuO 1-x -300, indicating that the mesoporous SiO 2 enhanced the dispersion of active Cu species. Meanwhile, the leaching Cu concentration was lower in CuO 1-x /SiO 2 -300 than CuO 1-x -300, which was also lower than that stated by WHO standard for drinking water, avoiding the secondary pollution. Due to confinement effect of mesoporous SiO 2 , CuO 1-x /SiO 2 -300 presented an excellent stability in cyclic experiments. ESR measurements revealed that rich active species such as ·OH, SO 4 ·- , O 2 ·- and 1 O 2 were generated in CuO 1-x /SiO 2 -300/PMS system. Quenching experiments revealed that these active species played an important role during the TC degradation, in which non-radical ( 1 O 2 ) pathway dominated, and the radical (·OH, SO 4 ·- and O 2 ·- ) pathway also presented innegligible influence simultaneously. This work blazed a new trail to activate PMS for removing TC from wastewater.
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