Lanthanide metal-organic frameworks as ratiometric fluorescent probes for real-time monitoring of PFOA photocatalytic degradation process

被引:1
|
作者
Song, Mingzhe [1 ]
Yu, Ruyue [1 ]
Shang, Yanxue [1 ]
Tashpulatov, Khurshid [2 ]
Sun, Hongman [1 ]
Zeng, Jingbin [1 ]
机构
[1] College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao,266580, China
[2] Samarkand State University Named After Sh.Rashidov, 140104, Uzbekistan
关键词
Catalysis - Energy transfer - Fluorescence - Fluorescence spectroscopy - Metal-Organic Frameworks - Organic polymers - Probes;
D O I
10.1016/j.chemosphere.2024.142946
中图分类号
学科分类号
摘要
The assessment of perfluorooctanoic acid (PFOA) photocatalytic degradation usually involves tedious pre-treatment and sophisticated instrumentation, making it impractical to evaluate the degradation process in real-time. Herein, we synthesized a series of lanthanide metal-organic frameworks (Ln-MOFs) with outstanding fluorescent sensing properties and applied them as luminescent probes in the photocatalytic degradation reaction of PFOA for real-time evaluation. As the catalytic reaction proceeds, the fluorescence color changes significantly from green to orange-red due to the different interaction mechanisms between the electron-deficient PFOA and smaller radius F− with the ratiometric fluorescent probe MOF-76 (Tb: Eu = 29:1). The limit of detection (LOD) was calculated to be 0.0127 mM for PFOA and 0.00746 mM for F−. In addition, the conversion rate of the catalytic reaction can be read directly based on the chromaticity value by establishing a three-dimensional relationship graph of G/R value-conversion rate-time (G/R indicates the ratio between green and red luminance values in the image.), allowing for real-time and rapid tracking of the PFOA degradation. The recoveries of PFOA and F− in the actual water samples were 99.3–102.7% (RSD = 2.2–4.4%) and 100.7–105.3% (RSD = 3.9–6.8%), respectively. Both theoretical calculations and experiments reveal that the detection mechanism was attributed to the photoinduced electron transfer and energy transfer between the analytes and the probe. This method simplifies the sample analysis process and avoids the use of bulky instruments, and thus has great potential on the design and development of quantitative time-resolved visualization methods to assess catalytic performance and reveal mechanisms. © 2024 Elsevier Ltd
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