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Development of headspace solid-phase microextraction/attenuated total reflection infrared chemical sensing method for the determiantionof volatile organic compounds in aqueous solutions

机译:顶空固相微萃取/衰减全反射红外化学传感方法测定水溶液中挥发性有机化合物的开发

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摘要

In this paper, a new method was developed by applying the principle ofheadspace solid-phase microextraction (HSSPM the attenuated total reflection (ATR) infrared (IR) chemical sensing method. This method is highly suitable for the detection of volatile organic compounds (VOCs) in aqueous solutions because it effectively eliminates the problems associated in soaking type of SPME-ATR-IR method. To facilitate the detection of VOCs in headspace, a specially designed sample cell is proposed that permits direct examination of the VOCs in the aqueous solution. Factors that influenced the IRsignals in this method such as the effect of agitation, headspace volume, sample volume, and temperature were examined in this work. Results showed that this method was fast and typical time to reach the maximum analytical signals was around 20 min. By applying agitation to the aqueous solution, much stronger analytical signals were observed, especially for lower volatility compounds. The headspace volume influenced the analytical signals strongly, especially for lower volatile compounds. An increase in the sample volume also results in higher analytical signals but these analytical signals are limited to a certain value. By examining five VOCs with different volatility's, the obtained linear regression coefficients (R-square) on standard curves in the concentration range of 5-200 ppm were higher than 0.99 and the typical detection limit using this method was around a few hundred ppb. This method can be used repeatedly because the time for regenerating the sensing element can be shorter than 5 min.
机译:本文采用顶空固相微萃取原理(HSSPM,衰减全反射(ATR)红外(IR)化学传感方法)开发了一种新方法,该方法非常适用于挥发性有机化合物(VOC)的检测。由于它可以有效消除SPME-ATR-IR方法的浸泡型方法带来的相关问题,因此,为了方便检测顶空中的VOC,建议使用专门设计的样品池,直接检测水溶液中的VOC。在这项工作中检查了影响该方法中IR信号的因素,例如搅拌,顶空体积,样品体积和温度的影响,结果表明该方法快速,达到最大分析信号的典型时间为20分钟左右。对水溶液进行搅拌,观察到更强的分析信号,尤其是对于挥发性较低的化合物。强烈影响分析信号,特别是对于挥发性较低的化合物。样品量的增加也会导致较高的分析信号,但是这些分析信号被限制为某个值。通过检查五个挥发性不同的VOC,标准曲线在5-200 ppm浓度范围内获得的线性回归系数(R平方)高于0.99,使用此方法的典型检测极限约为数百ppb。由于用于再生感测元件的时间可以短于5分钟,因此该方法可以重复使用。

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