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Trace determination of linear alkylbenzene sulfonates using ionic liquid based ultrasound-assisted dispersive liquid-liquid microextraction and response surface methodology

机译:离子液体基超声辅助分散液液微萃取和响应面法测定痕量直链烷基苯磺酸盐

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摘要

A new method was developed for determination of linear alkylbenzene sulfonates (LASs) in environmental water samples using ionic liquid based ultrasound-assisted dispersive liquid-liquid microextraction (IL-USA-DLLME) coupled with spectrophotometry detection. Different operational conditions affecting extraction efficiency of LASs including pH, volume of extraction solvent, methylene blue (MB) concentration, salt concentration and sonication time were studied via central composite design (CCD) optimization method. The statistical parameters of the model were F= 39.01 and R~2 = 0.9254. The optimal conditions were 8.3 for sample pH, 72 μL for extraction solvent, 49.2 μg mL~(-1) for MB concentration, 17.2% (w/v) for sodium chloride concentration and 30 s for sonication time. Under the optimal conditions, a calibration curve was obtained with linear dynamic range between 0.8 and 100 ng mL~(-1) and detection limit of 0.37 ng mL~(-1). The relative standard deviation (RSD %, n = 5) for the extraction and determination of 40.0 ng mL~(-1) of linear alkylbenzene sulfonates in the aqueous samples was obtained as 2.0%. The proposed method was successfully applied to determine concentrations of LASs in different non-spiked aqueous samples and satisfactory results were obtained.
机译:建立了一种基于离子液体的超声辅助分散液-液微萃取(IL-USA-DLLME)结合分光光度法检测环境水样中线性烷基苯磺酸盐(LASs)的新方法。通过中心复合设计(CCD)优化方法研究了影响LAS萃取效率的不同操作条件,包括pH,萃取溶剂体积,亚甲基蓝(MB)浓度,盐浓度和超声处理时间。模型的统计参数为F = 39.01和R〜2 = 0.9254。最佳条件为:样品pH值为8.3,萃取溶剂为72μL,MB浓度为49.2μgmL〜(-1),氯化钠浓度为17.2%(w / v),超声处理时间为30 s。在最佳条件下,得到的线性动态范围为0.8〜100 ng mL〜(-1),检出限为0.37 ng mL〜(-1)。提取和测定水性样品中线性烷基苯磺酸盐的40.0 ng mL〜(-1)的相对标准偏差(RSD%,n = 5)为2.0%。所提出的方法已成功地用于测定不同非加标水样中LAS的浓度,并获得了满意的结果。

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