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Photocatalytic persulfate activation by silica microsphere-supported g-C3N4 for efficient carbamazepine degradation
被引:5
|作者:
Li, Rui
[1
]
Wu, Zewei
[1
]
Yang, Yiyun
[2
]
Sun, Sijia
[1
]
Ma, Ruixin
[3
]
Ding, Hao
[1
]
机构:
[1] China Univ Geosci Beijing, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmet Minerals & Sol, Natl Lab Mineral Mat, Xueyuan Rd, Beijing 100083, Peoples R China
[2] China Univ Geosci Beijing, Sch Water Resources & Environm, Xueyuan Rd, Beijing 100083, Peoples R China
[3] North China Inst Sci & Technol, Langfang 065201, Hebei, Peoples R China
关键词:
g-C3N4;
Silica;
Composite photocatalyst;
Photocatalytic degradation;
CARE PRODUCTS PPCPS;
HYDROXYL RADICALS;
CARBON NITRIDE;
RATE CONSTANTS;
PHARMACEUTICALS;
SULFATE;
REMOVAL;
D O I:
10.1016/j.mssp.2024.108792
中图分类号:
TM [电工技术];
TN [电子技术、通信技术];
学科分类号:
0808 ;
0809 ;
摘要:
A silica-loaded g-C3N4 composite photocatalyst (M-SiO2/g-C3N4) was prepared by grinding amorphous SiO2 microspheres (M - SiO2) with melamine and calcining the resulting grinding products. This composite was used for photocatalytic persulfate (PMS) activation to degrade carbamazepine (CBZ). The results showed that the degradation efficiencies of CBZ by M-SiO2/g-C3N4-2.5 (39.16% of g-C3N4)-activated PMS were 78.92% and 100 % after simulated sunlight irradiation for 60 and 120 min, respectively. These values were significantly greater than those of the system with pure g-C3N4 (29.15 % and 42.4 %). In particular, the degradation efficiency of CBZ with M-SiO2/g-C3N4-2.5 decreased by only 9.47 % after 4 cycles of recycling. In the catalytic process, h(+), SO4 center dot- and O-2(center dot-) were the main reactive species contributing to CBZ degradation. Compared with g-C3N4, loading g-C3N4 on the surface of M - SiO2 resulted in a decrease in g-C3N4 lamellar stacking, which increased the number of active surface sites and improved the separation and migration of photogenerated carriers, improving the degradation performance.
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页数:11
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