Enhanced peroxymonosulfate activation for Orange I degradation by g-C3N4/AgFeO2 composite in water

被引:12
|
作者
Zhao, Ying [1 ]
Wang, Shuo [1 ]
Wei, Tong [1 ]
Ren, Yueming [1 ]
Luan, Tianzhu [2 ]
机构
[1] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Harbin 150001, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 1, Harbin 150001, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Delafossite; G-C3N4; Peroxymonosulfate; Heterogeneous catalysis; AZO-DYE; BIOELECTROCHEMICAL SYSTEM; HETEROGENEOUS ACTIVATION; SELECTIVE DEGRADATION; ORGANIC POLLUTANTS; ADVANCED OXIDATION; SULFATE; CATALYST; G-C3N4; AGFEO2;
D O I
10.1016/j.jece.2022.107241
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The construction of heterogeneous catalysts with high efficiency is significant for the degradation of persistent contaminants. Herein, the g-C3N4/AgFeO2 composite was fabricated and its composition, morphology and structure were systematically characterized. g-C3N4/AgFeO2 exhibited boosting peroxymonosulfate (PMS) cat-alytic performance on the degradation of Orange I (OI) than pure AgFeO2. It was optimized that the elimination of OI could be enhanced to 91%, with a kinetic rate of 0.076 min(-1). Such enhancement was attributed to the increment of low-valent metal species (Ag-0/Ag+, Fe2+/Fe3+) on AgFeO2 surface after coupling with g-C3N4, additionally, the synergy of g-C3N4 and AgFeO2 endowed the g-C3N4/AgFeO2 composite with higher conduc-tivity and more electron transfer, thereby promoting effective PMS decomposition. The leaching of metal ions in the g-C3N4/AgFeO2/PMS system was suppressed, which brought superior reusability and stability. It was verified that (O2,O2 center dot-,SO4 center dot-)-O-1 and center dot OH acting as the key reactive oxygen species contributed to the OI removal. Our findings provided valuable insights into the design of efficient and stable g-C3N4-based organometallic composites for advanced oxidation processes.
引用
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页数:11
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