季铵聚合物离子液体基气泡增强分散固相萃取法测定再生水中5种磺胺类抗生素及其相互作用机理

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ming Gao, Yu Liu, Su Ma, Sai Ma, Xuedong Wang and Yanyan Li
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引用次数: 0

摘要

本文制备了两种季铵盐聚合物离子液体(pil),并利用SEM、FT-IR和1H NMR对其进行了表征。以白芨微珠为萃取剂、酒石酸为酸源、NaHCO3为碱源、水溶性淀粉为填料的泡腾片为研究对象,建立了白芨微珠为萃取剂的泡腾片发泡增强分散固相萃取(PILE-d-SPE)方法。磺胺类抗生素(磺胺类抗生素)表面的正电荷和正电荷表现出明显的静电吸引力,从而增强了两种磺胺类抗生素与磺胺类抗生素之间的相互作用。P[VBTEA]Cl对5种sa的萃取率高于P[VBTEA]Cl,这可能是因为P[VBTEA]Cl的结构中含有更多的-OH官能团。提取前后,两种pil的FT-IR光谱与O-H和C-H拉伸振动吸收波段有显著差异。DFT计算表明,P[VBTHEA]Cl与SDM之间形成的强氢键导致结合能最高,因此SDM提取回收率最高。综上所示,氢键诱导效应是P[VBTEA]Cl萃取效率优于P[VBTEA]Cl的主要原因。采用单因素法,优化了再生水中砷含量测定的几个重要变量:萃取剂为200 mg pil,洗脱溶剂为400 μ l丙酮,洗脱时间为5 min。结合HPLC-DAD检测,对5种sa的检出限较低(0.19 ~ 0.32 μg L−1),加样回收率为78.4 ~ 99.7%,具有较好的分析效果。因此,基于P[VBTHEA] cl的E-d-SPE方法环保、省时、易于操作,具有优异的分析性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quaternary ammonium polymeric ionic liquid-based effervescence-enhanced dispersive solid-phase extraction for determining five sulfonamide antibiotics in reclaimed waters and their underlying interaction mechanisms†

Quaternary ammonium polymeric ionic liquid-based effervescence-enhanced dispersive solid-phase extraction for determining five sulfonamide antibiotics in reclaimed waters and their underlying interaction mechanisms†

Herein, two kinds of quaternary ammonium polymeric ionic liquids (PILs) were prepared and rigorously characterized based on SEM, FT-IR, and 1H NMR data. The PIL-based effervescence-enhanced dispersive solid-phase extraction (PILE-d-SPE) method was developed based on effervescent tablets containing PILs as extractants, tartaric acid as the acid source, NaHCO3 as the alkaline source, and water-soluble starch as the filler. The positive charges on the surface of PILs and the negative charges on the surface of sulfonamide antibiotics (SAs) exhibited significant electrostatic attraction, thereby enhancing interactions between two PILs and SAs. P[VBTHEA]Cl exhibited higher extraction efficiency for five SAs than P[VBTEA]Cl, possibly because the structure of P[VBTHEA]Cl contained more –OH functional groups compared to that of P[VBTEA]Cl. Before and after extraction, the FT-IR spectra of the two PILs were significantly different from the O–H and C–H stretching–vibration absorption bands. DFT calculations show that the strong hydrogen bonds formed between P[VBTHEA]Cl and SDM resulted in the highest binding energy and, consequently, the highest SDM extraction recovery rate. Overall, the H-bonding induction effect was inferred to be the main reason for the superiority of P[VBTHEA]Cl over P[VBTEA]Cl in extraction efficiency. Using the one-factor-at-a-time approach, several important variables were optimized for determining SAs in reclaimed waters as follows: 200-mg PILs as extractants, 400-μL acetone as elution solvent, and 5-min elution. By integration with HPLC-DAD detection, this approach provided satisfactory analytical performance: a low detection limit (0.19–0.32 μg L−1) and appropriately fortified recovery (78.4–99.7%) for five SAs. Consequently, the P[VBTHEA]Cl-based E-d-SPE method is environmentally friendly, time-saving, easy to operate, and exhibits excellent analytical performance.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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