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Purge-and-trap capillary gas chromatography with atomic emission detection for volatile halogenated organic compounds determination in waters and beverages

机译:具有原子发射检测功能的吹扫捕集毛细管气相色谱法测定水和饮料中的挥发性卤代有机化合物

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A method for the simultaneous determination of 10 volatile halogenated organic compounds (VHOCs), including four trihalomethanes (THMs), in waters and beverages was developed. The analytes were stripped from the aqueous sample by a flow of helium, preconcentrated in a capillary trap and thermally desorbed using a purge-and-trap (PT) system. This was followed by capillary gas chromatography with microwave-induced plasma atomic emission spectrometry (GC-AED). For element-specific detection, three wavelengths were monitored, corresponding to chlorine (479 nm), bromine (478 nm) and iodine (193 nm). Each chromatographic run took 21 min, including the purge time. After careful choice of the experimental conditions, the performance of the system was evaluated. Calibration curves were obtained by plotting peak area versus concentration and the correlation coefficients for linear calibration were at least 0.9987. Detection limits, calculated for 5 ml sample volume, ranged from 0.05 mug l(-1) for chloroform to 0.5 mug l(-1) for tetrachloromethane. The method was successfully applied to the quantitative analysis of water samples of different origin and also of several beer and juice samples. The tap water samples analyzed contain variable concentrations of the four trihalomethanes, ranging from 1.0 to 66.5 mug l(-1), depending of the compound. Whereas chloroform, bromodichloromethane and bromoform were found in some of the juice samples, only chloroform was detected in the beer samples. The method is reliable and can be used for routine monitoring in water and beverages. (C) 2004 Elsevier B.V. All rights reserved.
机译:开发了一种同时测定水和饮料中10种挥发性卤代有机化合物(VHOCs)的方法,其中包括4种三卤甲烷(THMs)。通过氦气流从含水样品中剥离分析物,在毛细管捕集阱中进行预浓缩,并使用吹扫捕集(PT)系统进行热脱附。然后进行毛细管气相色谱和微波诱导等离子体原子发射光谱法(GC-AED)。对于特定于元素的检测,监测了三个波长,分别对应于氯(479 nm),溴(478 nm)和碘(193 nm)。每次色谱分析都需要21分钟,包括吹扫时间。在仔细选择实验条件后,评估了系统的性能。通过绘制峰面积对浓度的曲线获得校准曲线,线性校准的相关系数至少为0.9987。以5毫升样品体积计算的检出限,从氯仿0.05杯l(-1)到四氯甲烷0.5杯l(-1)不等。该方法已成功应用于不同来源的水样品以及啤酒和果汁样品的定量分析。分析的自来水样品包含四种三卤甲烷的浓度可变,范围从1.0到66.5马克杯l(-1),具体取决于化合物。在一些果汁样品中发现了氯仿,溴二氯甲烷和溴仿,而在啤酒样品中仅检测到了氯仿。该方法可靠,可用于水和饮料的常规监测。 (C)2004 Elsevier B.V.保留所有权利。

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