期刊
JOURNAL OF HAZARDOUS MATERIALS
卷 401, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.jhazmat.2020.123326
关键词
Catalyst; Heterogeneous activation; Sulfate radical anion; Degradation
资金
- MOST, Taiwan [MOST 106-2221-E-992-302-MY3]
The CoO@mpgCN/PMS system showed high catalytic reactivity and SMX removal efficiency over a wide pH range, with stable and consistent degradation capacity for at least five consecutive cycles. The significant catalysis performance was attributed to the uniformly distributed mesopores, large specific surface area, and high electron transfer ability of CoO@mpgCN at the active CoO sites, leading to a radical chain reaction mechanism for SMX degradation.
A facile impregnation method was used to fabricate a hybrid CoO-3D ordered mesoporous carbon nitride (CoO@ mpgCN) catalyst that effectively activated peroxymonosulfate (PMS) for the degradation of pharmaceutical chemical, exemplified by antibiotic sulfamethoxazole (SMX) in aqueous solutions. The CoO@mpgCN/PMS system exhibited high catalytic reactivity and SMX removal efficiency over a wide pH range with an observed rate constant (k(obs)) of 0.314 min(-1). Furthermore, CoO@mpgCN was stable with consistently high degree of SMX degradation without having cobalt dissolution and loss of catalytic activity for at least five consecutive cycles. The significant catalysis performance of CoO@mpgCN was due to its uniformly distributed mesopores, large specific surface area, and high electron transfer ability at the active CoO sites. Both quenching experiments and electron paramagnetic resonance (EPR) analysis verified the yield, in abundance, of highly active species, specifically SO4- and (OH)-O-center dot from the CoO@mpgCN activation of PMS, primarily. Hence, SMX degradation followed a radical chain reaction mechanism. The result of this study revealed a novel prospective of CoO@mpgCN composite as PMS activator for the remediation of recalcitrant pollutants in water.
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