Qi Li, Hanqing Liu, Yigeng Wang, Xianjin Huang, Yao Huang, Zhehui Weng, Dandan Ge, Yingzhen Wang
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引用次数: 0
摘要
在这项工作中,首次使用六氟丁醇(HFB)和法呢醇(FO)制备了一种新型超分子溶剂(SUPRAS)。FO 起着双亲作用,HFB 起着凝聚诱导剂和密度调节剂的作用。利用制备的 SUPRAS,建立了分散液-液微萃取-高效液相色谱法,并辅以涡旋技术,用于测定水样中的苏丹红。对萃取参数(包括 FO 含量、HFB 含量、涡旋时间、盐添加量和溶液 pH 值)进行了深入研究和优化。在优化条件下,苏丹红 I 的线性范围为 10-750 纳克/毫升,苏丹红 III 和苏丹红 IV 的线性范围分别为 10-1000 纳克/毫升。苏丹染料的检测限为 0.8-3.1 纳克/毫升。苏丹染料的日间和日内相对标准偏差分别为 1.3%-4.1%和 0.2%-2.6%。最后,将该方法应用于饮料和河水样品中苏丹红的测定,回收率为 93.9% 至 122.1%。与提取实际样品中苏丹红染料的传统技术相比,所提出的方法更简单、更快速、更环保。
Preparation of a New Hexafluorobutanol-Farnesol Based Supramolecular Solvent and Its Application in Microextraction of Sudan Dyes From Beverage and Water Samples
In this work, a new supramolecular solvent (SUPRAS) was prepared for the first time using hexafluorobutanol (HFB) and farnesol (FO). FO acts as an amphiphile and HFB as a coacervation inducer and density regulator. The method of dispersive liquid-liquid microextraction followed by high-performance liquid chromatography, supported by a vortex technique, was established using the prepared SUPRAS for the determination of Sudan dyes in aqueous samples. The extraction parameters, including FO content, HFB content, vortex time, salt addition, and solution pH, were thoroughly investigated and optimized. Under the optimized conditions, the linearity range is 10–750 ng/mL for Sudan I, and 10–1000 ng/mL for Sudan III and Sudan IV, respectively. The limits of detection for Sudan dyes were in the range of 0.8–3.1 ng/mL. The inter- and intra-day relative standard deviations for Sudan dyes were in the range of 1.3%–4.1% and 0.2%–2.6%, respectively. Finally, the proposed method was applied to the determination of Sudan dyes in beverage and river water samples with recoveries ranging from 93.9% to 122.1%. Compared to conventional techniques for the extraction of Sudan dyes in real samples, the proposed method is simpler, faster, and more environmentally friendly.
期刊介绍:
The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.