Ratiometric Monitoring of Thorium Contamination in Natural Water Using a Dual-Emission Luminescent Europium Organic Framework

Traditional analytical methods of thorium contamination suffer from several disadvantages such as time-consuming procedures and an equipment-intensive nature, leading to substantial challenges in rapid and on-site monitoring of thorium concentrations in complex natural water systems. We report here...

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Veröffentlicht in:Environmental science & technology 2019-01, Vol.53 (1), p.332-341
Hauptverfasser: Liu, Wei, Dai, Xing, Wang, Yanlong, Song, Liping, Zhang, Linjuan, Zhang, Duo, Xie, Jian, Chen, Long, Diwu, Juan, Wang, Jianqiang, Chai, Zhifang, Wang, Shuao
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Sprache:eng
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Zusammenfassung:Traditional analytical methods of thorium contamination suffer from several disadvantages such as time-consuming procedures and an equipment-intensive nature, leading to substantial challenges in rapid and on-site monitoring of thorium concentrations in complex natural water systems. We report here the first case of a luminescent metal organic framework based probe (ThP-1) for highly sensitive and selective self-calibrated sensing of Th4+ contamination in natural fresh water media with a notably facilitated detection procedure. The detection limit of ThP-1 was determined to be 24.2 μg/L, much lower than the thorium contamination standard of 246 μg/L in drinking water defined by the World Health Organization. Importantly, the detection procedure based on the rarely reported self-calibration manner is greatly beneficial in improving the detection accuracy. The self-calibrated luminescence evolution process shows a great anti-interference ability capable of detecting thorium contamination in a wide concentration range from 24.2 μg/L to 300 mg/L, which can not be achieved directly by the traditional methods. The Th4+-selective luminescence response originates from the selective uptake and efficient enrichment of Th4+ by the host framework of ThP-1 through inner-sphere coordination, which is further confirmed by batch experiments, X-ray absorption spectroscopic study, and DFT calculations.
ISSN:0013-936X
1520-5851
DOI:10.1021/acs.est.8b04728