首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Air-assisted liquid-liquid microextraction based on solidification of floating deep eutectic solvent for the analysis of ultraviolet filters in water samples by high performance liquid chromatography with the aid of response surface methodology
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Air-assisted liquid-liquid microextraction based on solidification of floating deep eutectic solvent for the analysis of ultraviolet filters in water samples by high performance liquid chromatography with the aid of response surface methodology

机译:基于空气辅助液 - 液微萃取,基于浮动深对共晶溶剂的凝固,通过高效液相色谱法分析水样中的紫外线过滤器借助于反应表面方法

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For this work, a novel air-assisted liquid-liquid microextraction based on solidification of floating deep eutectic solvent (AA-LLME-SFDES), coupled with a high performance liquid chromatography (HPLC) method was developed for the detection of benzophenone and salicylate ultraviolet filters in water samples. Three types of fatty acid-based hydrophobic deep eutectic solvents (DESs) with low viscosity, low-density, and melting point close to room temperature were prepared and employed as extraction solvents. This air-assisted liquid-liquid microextraction was carried out in a glass centrifuge tube. Subsequently, the glass tube was introduced into ice-water bath and held for 3 min, during which the upper DES phase was solidified. The water phase was easily extracted using a syringe equipped with a long needle, and later, the glass tube was removed from ice-water bath. The solidified DES phase was immediately melted at room temperature and used for HPLC analysis. The response surface methodology was employed to optimize some influencing parameters such as the volume of the extraction solvent, the pH value of sample solution, the number of extraction cycles, and the addition of salt. A quadratic model, namely a central composite design, was used to replace the conventional single factor analysis. It was found that under optimal conditions, the limits of determination and quantification were 0.045-0.54 mu g L-1 and 0.15-2.0 mu g L-1, respectively. The relative standard deviations for inter-day (n = 5) and intra-day (n = 5) precision were <= 4.2%, whereas the enrichment factors for the ultraviolet filters were obtained from 41 to 50. Furthermore, this novel method was successfully employed for the detection of benzophenone and salicylate ultraviolet filters from real water samples. The recoveries ranged from 87.5% to 105.8%, whereas the RSDs were lower than 3.6%. (C) 2020 Elsevier B.V. All rights reserved.
机译:对于这项工作,基于浮动深对共晶溶剂(AA-LLME-SFDE)的凝固的新型空气辅助液 - 液微萃取,与高效液相色谱(HPLC)方法进行了用于检测二苯甲酮和水杨酸盐紫外线水样中的过滤器。制备三种类型的脂肪酸基疏水性深凝胶(DES),具有靠近室温的低粘度,低密度和熔点,并用作萃取溶剂。该空气辅助液液微萃取在玻璃离心管中进行。随后,将玻璃管引入冰水浴中并保持3分钟,在此期间凝固上层阶段。使用装有长针的注射器容易地提取水相,然后从冰水浴中除去玻璃管。固化的DES相立即在室温下熔化并用于HPLC分析。采用响应面方法来优化一些影响诸如提取溶剂的体积,样品溶液的pH值,提取循环的数量,以及加入盐的增加。二次模型,即中央复合设计,用于取代传统的单因素分析。发现在最佳条件下,测定和定量的极限分别为0.045-0.54μg1-1和0.15-2.0μg1-1。日内(n = 5)和白天(n = 5)精度的相对标准偏差为<= 4.2%,而紫外线过滤器的富集因子从41-50获得。此外,这种新方法是成功用于检测来自真实水样的二苯甲酮和水杨酸盐紫外线过滤器。回收率范围为87.5%至105.8%,而RSDS低于3.6%。 (c)2020 Elsevier B.v.保留所有权利。

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