首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Separation and determination of benzene, toluene, ethylbenzene and o-xylene compounds in water using directly suspended droplet microextraction coupled with gas chromatography-flame ionization detector
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Separation and determination of benzene, toluene, ethylbenzene and o-xylene compounds in water using directly suspended droplet microextraction coupled with gas chromatography-flame ionization detector

机译:直接悬浮液滴微萃取-气相色谱-火焰电离检测器分离和测定水中的苯,甲苯,乙苯和邻二甲苯化合物

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摘要

The directly suspended droplet microextraction (DSDME) technique coupled with the capillary gas chromatography-flame ionization detector (GC-FID) Was used to determine BTEX compounds in aqueous samples. The effective parameters such as organic solvent, extraction time, microdroplet Volume, salt effect and stirring speed were optimized. The performance of the proposed technique was evaluated for the detemination of BTEX compounds in natural water samples. Under the optimal conditions the enrichment factors ranged from 142.68 to 312.13, linear range: 0.01-20 mu g mL(-1), limits of detection; 0.8-7 ng mL(-1) for most analytes. Relative standard deviations for 0.2 mu g mL(-1) of BTEX in water were in the range 1.81-2.47% (n = 5). The relative recoveries of BTEX from Surface water at spiking level of 0.2 mu g mL(-1) were in the range of 89.87-98.62%.
机译:直接悬浮液滴微萃取(DSDME)技术与毛细管气相色谱-火焰电离检测器(GC-FID)结合用于测定水性样品中的BTEX化合物。优化了有机溶剂,提取时间,微滴体积,盐效应和搅拌速度等有效参数。评价了所提出技术的性能,用于测定天然水样品中的BTEX化合物。在最佳条件下,富集因子的范围为142.68至312.13,线性范围:0.01-20μg mL(-1),检测极限;对于大多数分析物为0.8-7 ng mL(-1)。水中0.2μg mL(-1)的BTEX的相对标准偏差在1.81-2.47%的范围内(n = 5)。加标浓度为0.2μg mL(-1)时,地表水中BTEX的相对回收率在89.87-98.62%的范围内。

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