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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Quantification of organic acids in particulate matter by coupling of thermally assisted hydrolysis and methylation with thermodesorption-gas chromatography-mass spectrometry
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Quantification of organic acids in particulate matter by coupling of thermally assisted hydrolysis and methylation with thermodesorption-gas chromatography-mass spectrometry

机译:通过热解-气相色谱-质谱联用热辅助水解和甲基化对颗粒物中的有机酸进行定量

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摘要

A quantitative method for the determination of organic acids in atmospheric particles is developed. The method couples a derivatisation step (thermally assisted hydrolysis and methylation) and a Curie point pyrolyser as a thermal desorption technique and gas chromatography-mass spectrometry (CPP-GC-MS). Among the reagents tested (tetramethylammonium hydroxide (TMAH), tetramethylammonium acetate (TMAAc) and phenyltrimethylammonium hydroxide (TMPAH)), the best performance was found using TMAAc as a derivatisation reagent for the reaction time of 4s at 510 degrees C as heating temperature. Calibration was performed for a series of fatty acids (FA), dicarboxylic acids (DCA) and terpenoic acids (TA) under these conditions. Coefficients of determination (R-2) were between 0.94 and 0.98. Limits of detection (LOD) were in the nanogram-range between 0.1 and 3.6 ng. The method is applied on atmospheric particle samples to obtain the quantification reproducibility and quantification limits. Reproducibility was determined in terms of relative standard deviations (RSD) for ambient aerosol samples collected by a high-volume-sampler (HVS, RSD = 6-45%, n = 10) and a Berner impactor (BI, RSD = 5-34%, n = 10). Based on 24 h sampling time the developed method enables quantification of all three classes of acids for both sampling techniques. Calibration data and presented volume concentrations are compared with literature data. A comparison with an off-line methylation-CC-MS using BF3 as a derivatisation reagent and capillary electrophoresis coupled mass spectrometry (CE-MS) showed a good agreement. Minimal sample preparation is the main advantage of the developed method. Depending on the sensitivity requirements the present method can be a fast and simple alternative to GC-MS techniques with conventional sample preparation steps for semi-volatile organic acids.
机译:建立了测定大气颗粒中有机酸的定量方法。该方法结合了衍生化步骤(热辅助水解和甲基化)和居里点热解器作为热脱附技术和气相色谱-质谱联用技术(CPP-GC-MS)。在测试的试剂(氢氧化四甲基铵(TMAH),乙酸四甲基铵(TMAAc)和苯基三甲基氢氧化铵(TMPAH))中,使用TMAAc作为衍生试剂时,在510摄氏度作为加热温度的4s反应时间中发现了最佳性能。在这些条件下对一系列脂肪酸(FA),二羧酸(DCA)和萜烯酸(TA)进行了校准。测定系数(R-2)在0.94至0.98之间。检测限(LOD)在0.1到3.6 ng之间的纳克范围内。该方法应用于大气颗粒样品,以获得定量重现性和定量极限。重现性是通过相对定量标准偏差(RSD)来确定的,该标准偏差是由大容量采样器(HVS,RSD = 6-45%,n = 10)和伯纳撞击器(BI,RSD = 5-34)收集的环境气溶胶样本%,n = 10)。基于24小时的采样时间,开发的方法可以对两种采样技术的所有三类酸进行定量。将校正数据和显示的体积浓度与文献数据进行比较。与使用BF3作为衍生化试剂和毛细管电泳耦合质谱(CE-MS)的离线甲基化CC-MS的比较显示出很好的一致性。最少的样品制备是开发方法的主要优点。根据灵敏度要求,本方法可以作为具有半挥发性有机酸常规样品制备步骤的GC-MS技术的快速简便替代方法。

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