化学
盐酸四环素
光催化
降级(电信)
石墨烯
吸附
化学工程
复合数
氧化物
催化作用
吸收(声学)
四环素
污染物
苯并噻唑
辐照
复合材料
环境污染
盐酸盐
苯酚
偶联反应
镧系元素
激进的
纳米材料
核化学
多相催化
作者
Shuai Yan,Chenjia Yang,Xusheng Li,Mengyao She,Ping Liu,Jianli Li
标识
DOI:10.1021/acs.inorgchem.6c03424
摘要
Abstract Tetracycline hydrochloride is a common aquatic contaminant and poses significant risks to environmental and human health. However, developing high-performance removal materials with good recyclability remains a challenge. The electron-deficient benzothiadiazole linker endowed these frameworks with visible-light absorption capability, while lanthanide nodes regulated ligand–metal electronic coupling and graphene oxide-mediated interfacial charge transfer, creating efficient photocatalyst composites (Ln-MOFs/GO) for TC degradation. The graphene oxide loading was optimized to obtain Ho/10-GO, which achieved 84.6% degradation of 10 ppm tetracycline (TC) hydrochloride within 40 min under visible-light irradiation after dark adsorption equilibrium had been reached. Encapsulating the composite in sodium alginate gel maintained a high pollutant removal rate over 15 catalytic cycles and enabled simple material recovery. Mechanistic studies combining radical-trapping tests and DMPO-based EPR measurements confirmed the generation of •O2– and indicated that the O2/electron-mediated pathway plays a key role in TC degradation. Structure–property analysis showed that the photocatalytic performance results from the visible-light-responsive benzothiadiazole units and the formation of type II heterojunctions, which improve photogenerated carrier separation. Ho/10-GO@Alg was also applied to visible-light-driven condensation–cyclization synthesis of benzothiazole derivatives. This research provides an effective strategy for TC degradation and offers insights into treating TC contaminants in aquatic environments.
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