过硫酸盐
电子顺磁共振
钒
降级(电信)
激进的
分解
光化学
电子转移
化学
猝灭(荧光)
核化学
无机化学
荧光
有机化学
催化作用
计算机科学
量子力学
核磁共振
物理
电信
作者
Guodong Fang,Wenhui Wu,Cun Liu,Dionysios D. Dionysiou,Yamei Deng,Dongmei Zhou
标识
DOI:10.1016/j.apcatb.2016.09.006
摘要
In the present study, the activation of persulfate (PS) with vanadium (V) species for PCBs (2,4,4′-trichlorobiphenyl [PCB28]) degradation was investigated for the first time. It was found that V2O3 exhibited high catalytic activity toward PS decomposition for PCB28 degradation. Even under near neutral pH (7.4), PCB28 was efficiently degraded in V2O3/PS. Sulfate radical anions (SO4−) and hydroxyl radicals (OH) were produced from PS activation with V2O3 for PCB28 degradation, and were characterized with electron paramagnetic resonance (EPR) technique. Free radical quenching studies showed that ethanol inhibited PCB28 degradation, while tert-butyl alcohol enhanced PCB28 degradation via reductive dechlorination with alcohol radicals. The pathway of PCB28 degradation was proposed on the basis of GC–MS analysis of intermediates of PCB28 degradation in V2O3/PS. The mechanisms of PS activation are elucidated. It was found that V(III) in V2O3 activated PS to form SO4− and V(IV) (VO2) via electron transfer process, and the formed V(IV) further transferred an electron to PS to generate SO4− and V(V) (V6O13), which were supported with XRD analysis. Furthermore, both VO2 and V2O5 can activate PS for PCB28 degradation, indicating that V(IV) would be regenerated from the reduction of V(V) by persulfate ions (S2O82−) on the surface of V2O5 particles. These findings would help to better understand the interactions between naturally occurring V minerals and PS, and provide a novel activator for PS activation to degrade contaminants.
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