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Solid phase microextraction with temperature-programmed desorption for the analysis of iodination disinfection byproducts

机译:程序升温脱附的固相微萃取用于碘加碘消毒副产物的分析

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An analytical approach for the determination of chlorination and iodination disinfection byproducts based on solid-phase microextraction (SPME) was developed, Solid-phase microextraction presents a simple, rapid, sensitive, and solvent-free approach to sample preparation in which analytes in either air or water matrixes are extracted into the polymeric coating of an optical fiber. Analytes are subsequently thermally desorbed in the injection port of a gas chromatograph for separation, detection, and quantitation, Thermal degradation of iodoform was observed during desorption from a polyacrylate fiber in initial GC/MS and GC/ECD experiments, Experiments were designed to determine SPME conditions that would allow quantification without significant degradation of analytes. Isothermal and temperature-programmed thermal desorptions were evaluated for efficacy in transferring analytes with wide-ranging volatilities and thermal stabilities into chromatographic analysis columns, A temperature-programmed desorption (TPD) (120-200 degrees C at 5 degrees C/min with an on-column injection port or 150-200 degrees C at 25 degrees C/min with a split/splitless injection port) was able to efficiently remove analytes with wide-ranging volatilities without causing thermal degradation, The SPME-TPD method was linear over 2-3 orders of magnitude with an electron capture detector and detection limits were in the submicrogram per liter range, Precision and detection limits for selected trihalomethanes were comparable to those of EPA method 551. Extraction efficiencies were not affected by the presence of 10 mg/L soap, 15 mg/L sodium iodide, and 6000 mg/L sodium thiosulfate, The SPME-TPD technique was applied to the determination of iodination disinfection byproducts from individual precursor compounds using GC/MS and to the quantitation of iodoform at trace levels in a water recycle system using GC/ECD. [References: 27]
机译:开发了一种基于固相微萃取(SPME)的测定氯化和碘化消毒副产物的分析方法,固相微萃取为样品制备提供了一种简单,快速,灵敏且无溶剂的方法,其中空气中的分析物或将水基质提取到光纤的聚合物涂层中。随后将分析物在气相色谱仪的进样口中进行热解吸,以进行分离,检测和定量分析。在最初的GC / MS和GC / ECD实验中,从聚丙烯酸酯纤维中解吸的过程中观察到了碘仿的热降解,设计了实验以确定SPME无需定量分析物即可降解的条件。评估了等温和程序升温的热脱附在将范围广泛的挥发性和热稳定性的分析物转移到色谱分析柱中时的功效。程序升温脱附(TPD)(120-200摄氏度,5摄氏度/分钟, -柱进样口或以25°C / min的速度在150-200℃下使用不分流/不分流进样口)能够有效去除具有宽范围挥发度的分析物而不会引起热降解,SPME-TPD方法在2- 3个数量级的电子捕获检测器,检测极限在亚微克每升范围内,所选三卤代甲烷的精密度和检测极限与EPA方法551相当。萃取效率不受10 mg / L肥皂的影响,15 mg / L的碘化钠和6000 mg / L的硫代硫酸钠,采用SPME-TPD技术测定食盐中的碘化消毒副产物。使用GC / MS分离两个前体化合物,并使用GC / ECD在水循环系统中以痕量定量碘仿。 [参考:27]

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