Removal of tetracycline by ultraviolet/sodium percarbonate (UV/SPC)advanced oxidation process in water

化学 降级(电信) 紫外线 四环素 羟基自由基 核化学 高级氧化法 反应速率常数 环境化学 动力学 激进的 生物化学 抗生素 有机化学 材料科学 光电子学 催化作用 电信 物理 量子力学 计算机科学
作者
L.N. Zhao,Liang Guo,Chunji Jin,Dexiang Yang,Yanan Zhang,Progress Mupindu
出处
期刊:Environmental Research [Elsevier]
卷期号:247: 118260-118260 被引量:4
标识
DOI:10.1016/j.envres.2024.118260
摘要

Tetracycline (TC) was widely used and frequently detected in various water bodies, where the presence of TC posed a significant threat to the health of aquatic organisms. Furthermore, antibiotics were hardly degraded by biological treatment. Thus, in order to enhance the removal of TC, we proposed the use of a novel ultraviolet/sodium percarbonate (UV/SPC) advanced oxidation process and initiated an in-depth study. The study investigated the influence of oxidant dosage, initial pH, UV intensity, and TC concentration on the removal of TC. The results demonstrated that the UV/SPC system efficiently removed TC, with removal efficiency increasing as the SPC concentration increased. Within the pH range of 3–11, TC degradation exhibited minimal variation, indicating the UV/SPC system's strong adaptability to pH variations. The research on the impact of the water matrix on TC removal revealed that HCO3− had an inhibitory effect on TC degradation, while NO3− promoted TC degradation. Additionally, the presence of free radical species (·OH, ·CO3−, ·O2−) were detected and rate constants for the secondary reactions (k·OH,TC = 6.3 × 109 L mol−1·s−1, k·CO3-,TC = 3.4 × 108 L mol−1·s−1) were calculated, indicating that ·OH exhibited a stronger oxidative performance compared to ·CO3−. This study did not only present a novel strategy via UV/SPC to remove TC but also uncovered the unique role of ·CO3− for contaminant removal.
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