Magnetic ZIF-8 extraction using supramolecular solvent based on ferrofluid and vortex-assisted liquid–liquid microextraction of cationic dyes in beverage and river water samples

萃取(化学) 阳离子聚合 十二烷基硫酸钠 色谱法 溶剂 化学 检出限 罗丹明B 洗脱 核化学 有机化学 光催化 催化作用
作者
Yang Yu,Rong Zhang,Lurong Hao,Yanni Li,Baoling Wang,Dandan Ge
出处
期刊:Microchemical Journal [Elsevier]
卷期号:196: 109689-109689 被引量:3
标识
DOI:10.1016/j.microc.2023.109689
摘要

In this work, a new type of magnetic ZIF-8 based on ferrofluids (FFs) and supramolecular solvents (SUPRASs) was prepared and applied as an extraction phase in vortex-assisted liquid–liquid microextraction of cationic dyes (chrysoidin, auramine O and rhodamine B) in beverage and river water samples. The FFs comprised sodium dodecyl sulfate (SDS)-coupled titanium dioxide-coated MZIF-8 and hexafluorobutanol-geraniol SUPRAS (MZIF-8/SDS-TiO2@HFB-Ger). The prepared extraction phase exhibited high extraction recoveries of these cationic dyes owing to strong interaction mechanisms, including hydrogen-bonding, hydrophobic, π-π and electrostatic attractions, between the FFs and the analytes. The optimum extraction conditions of cationic dyes were as follows: Ger content was 4 %, HFB content was 6 %, MZIF-8/TiO2-SDS was 25 mg, vortex time was 3 min, solution pH was 6–8, salt concentration was 5 % (m/v), elution solvent was ethanol and elution solvent volume was 500 μL. Under the optimized conditions, cationic dyes were linear in 5–1000 ng mL−1 with determination coefficients higher than 0.9957. The limits of detection ranged from 1 to 1.5 ng mL−1, and the limits of quantification were between 3.5 and 5 ng mL−1. Finally, the developed method was applied to determine the target analytes in beverage and river water samples, achieving extraction recoveries ranging from 93.1 % to 104.3 %, with relative standard deviations between 1.1 % and 8.1 %. Compared with MZIF-8, MZIF-8/SDS-TiO2@HFB-Ger exhibited higher extraction efficiency for cationic dyes. Therefore, the developed method has great potential in extracting various analytes from various food and water samples.
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