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UiO-66-NH2: a recyclable and efficient sorbent for dispersive solid-phase extraction of fluorinated aromatic carboxylic acids from aqueous matrices
The present study describes the trace analysis of 23 fluorinated aromatic carboxylic acids based on the dispersive solid-phase extraction (dSPE) technique using UiO-66-NH 2 MOF as efficient, recyclable sorbent, and GC–MS negative ionization mass spectrometry (NICI MS) as determination technique. All...
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Published in: | Analytical and bioanalytical chemistry 2023-07, Vol.415 (17), p.3435-3448 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The present study describes the trace analysis of 23 fluorinated aromatic carboxylic acids based on the dispersive solid-phase extraction (dSPE) technique using UiO-66-NH
2
MOF as efficient, recyclable sorbent, and GC–MS negative ionization mass spectrometry (NICI MS) as determination technique. All 23 fluorobenzoic acids (FBAs) were enriched, separated, and eluted in a shorter retention time; the derivatization was done by pentafluorobenzyl bromide (1% in acetone), in which the use of inorganic base K
2
CO
3
was improved by triethylamine to increase the lifespan of the GC column. The performance of UiO-66-NH
2
was evaluated by dSPE in Milli-Q water, artificial seawater, and tap water samples, and the impact of various parameters on the extraction efficiency was investigated by GC-NICI MS. The method was found to be precise, reproducible, and applicable to the seawater samples. In the linearity range, the regression value was found to be >0.98; LOD and LOQ were found to be in the range of 0.33–1.17 ng/mL and 1.23–3.33 ng/mL, respectively; and the value of the extraction efficiency was found to range between 98.45 and 104.39% for Milli-Q water samples, 69.13–105.48% for salt-rich seawater samples, and 92.56–103.50% for tap water samples with a maximum RSD value of 6.87% that confirms the applicability of the method to different water matrices.
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ISSN: | 1618-2642 1618-2650 |
DOI: | 10.1007/s00216-023-04728-1 |