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Rapid determination of trace phenols migrating into drinking water from plastic-based pipe materials and household water treatment equipment using vortex-assisted emulsification microextraction

机译:涡旋乳化微萃取技术快速测定从塑料基管材和家用水处理设备中迁移到饮用水中的痕量苯酚

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A simple and rapid vortex-assisted emulsification microextraction (VAEME) method combined with spectrophotometry was developed for the determination of trace phenols migrating into potable water from plastic-based pipe materials and household water treatment equipments. The oxidative coupling reaction of phenolic compounds with 4-aminoantipyrine was carried out employing potassium peroxodisulfate as the oxidant in alkaline medium. A cloudy mixture was formed facilitating mass transfer of the reaction products into the fine droplets of toluene. The extraction equilibrium was rapidly achieved within 3 min by a combination of vibration and heating. The extract was concentrated in the narrow neck of the vessel, and could be easily withdrawn with a syringe. The VAEME method effectively avoids the analytical errors resulting from fluid leakage, which often occurs during conventional liquida€“liquid extraction with a separating funnel. Under the optimal conditions, linearity ranges of 0.2a€“180 ??g La?’1 and detection limits of 0.08 ??g La?’1 (expressed as C6H5OH concentration) were achieved. This approach was successfully applied in the determination of trace amounts of phenols in 36 solutions used to soak a variety of matrices. The recoveries were in the range of 86.0a€“99.8% and the relative standard deviations ranged from 0.53% to 6.5%. Compared with the official method, the proposed method was faster, more sensitive and required lower amounts of reagents.
机译:建立了一种简便快速的涡流辅助乳化微萃取(VAEME)方法与分光光度法相结合的方法,用于测定从塑料基管材和家用水处理设备迁移到饮用水中的痕量苯酚。以过二硫酸钾为氧化剂,在碱性介质中进行酚类化合物与4-氨基安替比林的氧化偶联反应。形成浑浊的混合物,以促进反应产物传质到甲苯的细小液滴中。通过振动和加热相结合,可在3分钟内迅速达到萃取平衡。提取物浓缩在容器的狭窄颈部,可以用注射器轻松取出。 VAEME方法有效地避免了由流体泄漏引起的分析误差,该误差通常发生在使用分液漏斗进行常规液体萃取过程中。在最佳条件下,线性范围为0.2a?180?g La?'1,检测极限为0.08?g La?'1(表示为C6H5OH浓度)。该方法成功地用于测定36种浸泡各种基质的溶液中的痕量苯酚。回收率在86.0%至99.8%之间,相对标准偏差在0.53%至6.5%之间。与官方方法相比,该方法更快,更灵敏,所需试剂更少。

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