Flower-like imide covalent organic framework as an electrochemical platform catcher for simultaneous sensitive detection of trace Pb(II) and Cd(II)

检出限 电化学 吸附 水溶液中的金属离子 共价键 线性范围 X射线光电子能谱 化学 金属 化学工程 电极 色谱法 物理化学 有机化学 工程类
作者
Ru Zhang,Junhui Yu,Haiou Chen,Yu Zhou,Xiangjun Yang,Li-Lian Wang,Huiping Bai
出处
期刊:Microchemical Journal [Elsevier]
卷期号:193: 109165-109165 被引量:2
标识
DOI:10.1016/j.microc.2023.109165
摘要

Heavy metal pollution in aquatic environment poses an enormous risk to ecosystems and human health. In this study, a flowerlike covalent organic framework (TpTa-COF) was synthesized by one-step solvothermal method with 2,4,6-triformylphloroglucinol (Tp) and 4, 4-diamino-tribiphenyl (Ta) as building elements. Then it was used as an effective trap to establish an electrochemical sensing platform for simultaneously sensitive detection of trace Pb(II) and Cd(II) in water. This three-dimensional flower-shaped structure exhibited exceptional adsorption capacity, large surface area, high stability, and all of which enhanced the detection sensitivity of the sensor and facilitated full contact between ions and substrate. The high oxygen content in the structure provided abundant active sites for Pb(II) and Cd(II), further enhancing its electrochemical response. The constructed sensor exhibited a linear response to Pb(II) within the concentration range of 3–60 µg/L under the optimal conditions, with a detection limit of 0.16 µg/L. Similarly, a linear response was observed for Cd(II) in the concentration range of 5–60 µg/L, with a detection limit of 0.29 µg/L. Low detection limits, excellent sensitivity, and strong stability were all features of the suggested approach. It has been successfully employed in determining Pb(II) and Cd(II) concentrations in two actual water samples. XPS, SEM-EDS mapping, and density functional theory calculations confirmed that TpTa-COF interacted with metal ions mainly via coordination with carbonyl oxygen atoms in the structure. Overall, these findings will broaden the applications of COF in the field of chemical analysis.
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