磺胺甲恶唑
化学
氧化磷酸化
核化学
环境化学
生物化学
抗生素
作者
Özge Dinç,Stanisław Wacławek,Rafael R. Solís,Dionysios D. Dionysiou
标识
DOI:10.1016/j.cej.2024.151085
摘要
The synergic effect of ferrate (VI) (Fe(VI)) and peroxymonosulfate (PMS) on sulfamethoxazole (SMX) oxidative removal was investigated in this study. The sulfate radicals (SO4−), generated through Fe(VI)-mediated activation of PMS, have been demonstrated as an effective oxidant for the removal of SMX. However, the scavenging experiments have suggested that various iron species, i.e., Fe(VI), Fe(V), and Fe(IV) play a vital role in facilitating efficient SMX oxidation. pH is a crucial parameter in this system because the involved species, including Fe(VI), PMS, and SMX, have acid-base dissociation points. Accordingly, the optimal pH value for the SMX removal was achieved at pH = 6, and the addition of PMS enhanced the degradation efficiency of Fe(VI) at all pH-operating conditions. Several oxidation products of SMX were identified, including sulfanilamide (SAM), 3-amino-5-methylisoxazole (AMI), and other potentially hydroxylated byproducts. Characterization studies on solid particles collected after the Fe(VI)/PMS treatment revealed structural changes during SMX oxidation, and the potential contributions of Fe2O3 or Fe(OH)3 to the oxidation mechanism were evaluated accordingly. While the removal efficiency in a river matrix was slightly reduced, the presence of inorganic ions had minimal impact on SMX removal, which confirms the high potential of the Fe(VI)/PMS technology to operate in environmentally relevant conditions.
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