A phenyl-functionalized nitrogen-rich magnetic hyper crosslinked polymer for magnetic solid-phase extraction of 5-nitroimidazoles residues in water and fish samples

A phenyl-functionalized nitrogen-rich magnetic hyper crosslinked polymer was prepared and used for the effective magnetic solid-phase extraction of 5-nitroimidazoles residues from water and fish samples. [Display omitted] •A phenyl-functionalized nitrogen-rich magnetic hyper crosslinked polymer was...

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Veröffentlicht in:Microchemical journal 2023-08, Vol.191, p.108936, Article 108936
Hauptverfasser: Wang, Juntao, Liu, Jiajia, Liu, Weihua, Liu, Ziwang, Wu, Qiuhua, Wang, Zhi, Yan, Hongyuan
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Sprache:eng
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Zusammenfassung:A phenyl-functionalized nitrogen-rich magnetic hyper crosslinked polymer was prepared and used for the effective magnetic solid-phase extraction of 5-nitroimidazoles residues from water and fish samples. [Display omitted] •A phenyl-functionalized nitrogen-rich magnetic hyper crosslinked polymer was prepared.•It was investigated for the magnetic solid-phase extraction of 5-nitroimidazoles.•It exhibited a good extraction capability for some 5-nitroimidazoles.•The new method was suitable for determination of the target analytes in real sample. A novel magnetic hyper crosslinked polymer (BTA-MHCP) was prepared by one-pot reaction of benzotriazole, 1,3,5-triphenylbenzene and phenyl-functionalized Fe3O4@SiO2. The BTA-MHCP was then investigated as the adsorbent for the rapid magnetic solid-phase extraction (MSPE) of the 5-nitroimidazoles (5-NDZs) including dimetridazole, metronidazole, secnidazole, ronidazole and ornidazole. The adsorbent showed good adsorption properties for the 5-NDZs. The key factors that affect the MSPE such as extraction time, the amount of sorbent, and the type of eluent and its volume were optimized. Under the optimal conditions, the linear response ranges for the established method were 0.15–100.0 ng mL−1 and 3.9–100.0 ng g−1 for drinking water and fish samples, respectively, with the coefficients of determination (r2) of 0.9981 to 0.9998. The limits of detection (S/N = 3) for the analytes were 0.02–0.05 ng mL−1 and 0.7–1.3 ng g−1, and the method recoveries ranged from 92.0% to 101.0% and from 89.9% to 104.0% for drinking water and fish samples, respectively.
ISSN:0026-265X
1095-9149
DOI:10.1016/j.microc.2023.108936