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Lanthanide metal-organic frameworks as ratiometric fluorescent probes for real-time monitoring of PFOA photocatalytic degradation process.
Song, Mingzhe; Yu, Ruyue; Shang, Yanxue; Tashpulatov, Khurshid; Sun, Hongman; Zeng, Jingbin.
  • Song M; College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao, 266580, China.
  • Yu R; College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao, 266580, China.
  • Shang Y; College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao, 266580, China.
  • Tashpulatov K; Samarkand State University Named After Sh.Rashidov, 140104, Uzbekistan.
  • Sun H; College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao, 266580, China. Electronic address: hongman.sun@upc.edu.cn.
  • Zeng J; College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao, 266580, China. Electronic address: xmuzjb@163.com.
Chemosphere ; 363: 142946, 2024 Sep.
Article en En | MEDLINE | ID: mdl-39059635
ABSTRACT
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 = 291). 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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Contaminantes Químicos del Agua / Caprilatos / Colorantes Fluorescentes / Fluorocarburos / Estructuras Metalorgánicas Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Contaminantes Químicos del Agua / Caprilatos / Colorantes Fluorescentes / Fluorocarburos / Estructuras Metalorgánicas Idioma: En Año: 2024 Tipo del documento: Article