TiO2/activated carbon synthesized by microwave-assisted heating for tetracycline photodegradation

催化作用 光催化 活性炭 光降解 盐酸四环素 材料科学 吸附 带隙 微波食品加热 分析化学(期刊) 光化学 可见光谱 炭黑 碳纤维 核化学 化学 有机化学 光电子学 四环素 复合材料 复合数 物理 天然橡胶 量子力学 生物化学 抗生素
作者
Wenya Ao,Junshen Qu,Haikuan Yu,Yang Liu,Chenglong Liu,Jie Fu,Jianjun Dai,Xiaotao Bi,Yadong Yuan,Yunfeng Jin
出处
期刊:Environmental Research [Elsevier]
卷期号:214: 113837-113837 被引量:20
标识
DOI:10.1016/j.envres.2022.113837
摘要

A furfural residue-derived activated carbon (AC) supported black-TiO2 photocatalyst was successfully prepared by ultrasonic-assisted sol-gel treatment (USG) and solvothermal treatment (ST) combined with microwave-assisted heating (MH). The prepared composites were characterized and evaluated based on the degradation of tetracycline hydrochloride (TC) under ultraviolet (UV) illumination. The average TiO2 nanoparticle size of the as-synthesized catalysts was between 9 and 11 nm. The bandgap of TiO2-USGM was 1.6 eV, much lower than that of other reference catalysts. Organic carbon and AC in the catalyst play positive roles in reducing the band gap (e.g. 1.6∼2.6 eV) and improving visible-light absorption. The oxygen vacancies are responsible for UV-visible absorption. Adding AC into black TiO2 resulted in a lower degree of recombination of photogenerated electrons. Mott-Schottky plots showed that AC-containing TiO2@AC-STM reduced the value of conduction band value from -0.59 eV to -0.24 eV, which is beneficial to photogenerated electrons. Compared with TiO2, the Ti-O-C and Ti-C- in TiO2@AC remarkably improved the adsorption and catalytic efficiency of TC. In a near-neutral pH environment, TiO2@AC-STM and TiO2@AC-USGM exhibited high removal efficiencies (88.0% and 75.7%, respectively) and degradation rates (0.0418 and 0.0302 μmol/g/s, respectively) at a catalyst load of 0.25 g/L. Notably, the catalyst can be effectively used over a wide range of pH (6-9). The solution pH after treatment was close to neutral, which is advantageous for wastewater treatment. The activation energies were found to be approximately 3.47 kJ/mol. The thermodynamic parameters showed that the photodegradation process was non-spontaneous and endothermic. Based on the trapping experiments, O2⋅- was mainly responsible for TC photodegradation over TiO2@AC-STM, followed by h+. The TC degradation pathways and catalyst stability were also investigated. Biomass-derived carbon-supported catalysts have great potential for waste biomass utilization as green, and low-cost catalysts.
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