化学
催化作用
激进的
电子顺磁共振
降级(电信)
核化学
食腐动物
无机化学
有机化学
电信
计算机科学
物理
核磁共振
作者
Thanh-Binh Nguyen,Van-Re Le,Ching Huang,Chiu‐Wen Chen,Lin‐Jer Chen,Cheng‐Di Dong
标识
DOI:10.1016/j.cej.2022.137326
摘要
• Ternary NiCo/Mn/GO catalyst was rationally sysnthesized. • NiCo/Mn/GO exhibited excellent electron transport capability and PMS activation. • CIP degradation by NiCo/Mn/GO + PMS system occurred over different water conditions. • Radicals and non-radicals were involved in CIP degradation by NiCo/Mn/GO + PMS. • NiCo/Mn/GO was sustainable in multiple cycles of CIP degradation efficiency. A catalyst, NiCo 2 O 4 /MnOOH/GO, was successfully synthesized by immobilizing NiCo 2 O 4 and graphene oxide (GO) on MnOOH for the activation of peroxymonosulfate (PMS) with enhanced catalytic activity in ciprofloxacin (CIP) degradation. Results demonstrated 99% removal of CIP (0.02 mM) in the NiCo/Mn/GO system after 30 min at 0.2 mM of PMS and 0.15 g/L of NiCo/Mn/GO. The effects of solution pH, catalyst dose, PMS concentration, major inorganic ions, and natural organic matter (NOM) on CIP degradation were studied. The NiCo/Mn/GO exhibited good sustainability in catalytic removal efficiency for multiple uses. Furthermore, scavenger tests and electron paramagnetic resonance (EPR) results showed that singlet oxygen ( 1 O 2 ), superoxide radicals (O 2 •- ), sulfate radicals (SO 4 •− ), and hydroxyl radicals (•OH) were generated in the NiCo/Mn/GO + PMS system and participated in CIP degradation. The NiCo/Mn/GO is a promising catalyst for PMS activation in the degradation of CIP and other emerging contaminants.
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