Preparation and immobilization of Bi2WO6/BiOI/g-C3N4 nanoparticles for the photocatalytic degradation of tetracycline and municipal waste transfer station leachate

被引:37
作者
Chu, Yanyang [1 ]
Fan, Jinruo [1 ]
Wang, Rong [1 ]
Liu, Chang [1 ]
Zheng, Xianglei [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266042, Shandong, Peoples R China
关键词
Bi2WO6/BiOI/g-C(3)N(4 )photocatalyst; Immobilization; Tetracycline degradation; Leachate degradation; Biodegradability enhancement; HETEROJUNCTION; PERFORMANCE; G-C3N4; WATER; MESH;
D O I
10.1016/j.seppur.2022.121867
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Bi2WO6/BiOI nanoparticles were embedded into graphitic carbon nitride (g-C3N4) to fabricate a new visible-light-driven photocatalyst (Bi2WO6/BiOI/g-C3N4). Furthermore, the immobilization of Bi2WO6/BiOI/g-C3N4 was performed by a new method characterized by using polytetrafluoroethylene (PTFE) as an adhesive agent and boric acid (H3BO3) as a pore-forming agent. Bi2WO6/BiOI/g-C3N4 possesses the higher photocatalytic performance than Bi2WO6/BiOI and g-C3N4 for tetracycline degradation because of the enhancement of light absorption and electron/hole (e(-)/h(+)) pairs separation. After immobilization, Bi2WO6/BiOI/g-C3N4 still remained considerable activity and stability. For the degradation of tetracycline, the immobilized photocatalyst presented the degradation rate of over 90 % within 120 min, whereas the photocatalytic degradation of municipal waste transfer station (MWTS) leachate for 28 h presented the chemical oxygen demand (COD) removal rate of 56.1 % and the total organic carbon (TOC) removal rate of 50.4 %. Additionally, the biodegradability of the two test solutions was enhanced evidently after the photocatalytic degradation. This work mainly provides a new photocatalyst immobilization method to promote the large-scale application of photocatalytic degradation.
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页数:15
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