At present, the mechanism difference between tetragonal BiVO4 (t-BiVO4) and monoclinic BiVO4 (m-BiVO4) coupled peroxymonosulfate (PMS) to realize photocatalysis is still unclear. In this study, m-BiVO4 and t-BiVO4 were obtained by adjusting the bismuth-vanadium ratio in the precursor solution (Bi:V=3:1; 1:1; 1:2 and 1:3). The results of photocatalytic experiments showed that both t-BiVO4 and m-BiVO4 had certain activation effects on PMS, and the prepared monoclinic B1V2 has the strongest photocatalytic performance. Using 20 mg B1V2 to activate 4 mmol L-1 PMS in 30 min, the degradation rate of tetracycline hydrochloride (TCH) reached 92.8%. The free radical quenching experiment and EPR test showed that when m-BiVO4 coupled PMS degraded TCH, the contribution of active species was SO4•->•OH>•O2->h+. Compared with m-BiVO4, the wide band gap of t-BiVO4 makes the photogenerated carrier recombination. When t-BiVO4 coupling PMS, the contribution of active species is •O2->SO4•->•OH>h+. In addition, the intermediate products of TCH degradation were analyzed by LC-MS, and three possible degradation paths of TCH were proposed.
Keywords: BiVO(4); Tetracycline hydrochloride; crystal phase regulation; peroxymonosulfate; photocatalysis.
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