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A ratiometric and selective fluorescent nanosensor for determining Hg2+ ions based on a novel functionalized metal–organic framework.
- Source :
-
Applied Organometallic Chemistry . Aug2024, Vol. 38 Issue 8, p1-13. 13p. - Publication Year :
- 2024
-
Abstract
- A new method using fluorescence was developed to detect Hg2+ ions in water. This method relied on the reaction between NH2‐MIL‐53(Al) and 5‐bromo‐2‐hydroxyacetophenone. The method was carefully fine‐tuned for optimal reaction conditions and analytical parameters like pH levels, nanosensor quantity, and detection limits. It showed great linearity in detecting Hg2+ ions in the range of 0.0–3.0 ppm (0.0–1.50 × 10−5 M), with a very low detection limit of 1.65 × 10−2 ppm (8.23 × 10−8 M). We tested how well the method can distinguish between different substances by investigating whether other common substances in water samples would interfere. The results were positive, as the presence of these substances did not significantly affect the accuracy of detecting Hg2+ ions, confirming the method's reliability. In order to confirm its dependability, we conducted a quantitative test to detect Hg2+ ions in water samples. The recovery rates obtained ranged from 97.16% to 103.2%, demonstrating the method's precision and accuracy. A comparison with inductively coupled plasma optical emission spectrometry (ICP‐OES), a well‐known method for analyzing trace metals, produced similar results, further instilling confidence in the 5Br2HA = N‐Al‐MOF nanosensor that was developed. In general, this research emphasizes the exciting potential of the new nanosensor in detecting Hg2+ ions in various water and cosmetic samples. It provides a strong and dependable alternative to traditional detection methods. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02682605
- Volume :
- 38
- Issue :
- 8
- Database :
- Academic Search Index
- Journal :
- Applied Organometallic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 178428322
- Full Text :
- https://doi.org/10.1002/aoc.7571