Enhanced photodegradation of tetracycline by novel porous g-C3N4 nanosheets under visible light irradiation

化学 光降解 辐照 多孔性 可见光谱 光化学 四环素 光催化 化学工程 有机化学 催化作用 光电子学 抗生素 生物化学 工程类 物理 核物理学
作者
Nothando A. Phakathi,Shepherd M. Tichapondwa,Evans M. N. Chirwa
出处
期刊:Journal of Photochemistry and Photobiology A-chemistry [Elsevier BV]
卷期号:462: 116252-116252 被引量:13
标识
DOI:10.1016/j.jphotochem.2024.116252
摘要

• Novel porous g-C 3 N 4 nanosheets were synthesised and characterized. • Porous g-C 3 N 4 nanosheets showed an enhanced efficiency on photodegradation of tetracycline under visible light irradiation. • The influence of catalyst mass, pH, tetracycline concentration and reusability were studied. • Investigations of ROS revealed that •O 2 − and h + are responsible for tetracycline degradation. • The photocatalytic mechanism of porous g-C 3 N 4 nanosheets was analysed. Harnessing photocatalysis to degrade recalcitrant organic pollutants is a potent solution to addressing water pollution and alleviating energy crisis. Photocatalysts possessing intriguing characteristics such as controllable band gap, efficient visible-light absorption and high photocatalytic activity play a pivotal role in this regard. Herein, porous g-C 3 N 4 nanosheets were synthesised via pyrocondensation polymerization with melamine and NH 4 HCO 3 and their photocatalytic performance was investigated for degradation of tetracycline. Characterization techniques including XRD, FTIR, SEM, TEM, BET and UV–Vis spectroscopy were employed and revealed that porous g-C 3 N 4 nanosheets increased light absorption capacity, provided more reactive sites and suppressed recombination of photogenerated electron-hole pairs, thus enhancing the material’s photodegradation efficiency in the degradation of tetracycline. Optimization studies showed that 83 % of tetracycline was removed after 2 h of visible light irradiation using 1 gL −1 catalyst loading, an initial concentration of 10 ppm and a solution pH of 7. The catalyst showed remarkable recyclability, retaining its chemical structure and functional properties, with 68 % degradation achieved after 5 cycles. Through radical scavenging experiments, superoxide radicals (•O 2 − ) and photogenerated hole (h + ) were identified as the primary active species responsible for TC degradation. A plausible photocatalytic mechanism was proposed from these experiments. This study provides a facile, cost effective, eco-conscious and effective approach for incorporating porous hierarchical and 2D nanosheets morphology on g-C 3 N 4 to enhance its photocatalytic performance under visible light.
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