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Pre-concentration of phenolic compounds in water samples by novel liquid-liquid microextraction and determination by gas chromatography-mass spectrometry

机译:新型液-液微萃取法对水样中的酚类化合物进行预浓缩并通过气相色谱-质谱法测定

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摘要

Pre-concentration and determination of 8 phenolic compounds in water samples has been achieved by in situ derivatization and using a new liquid-liquid microextraction coupled GC-MS system. Microextraction efficiency factors have been investigated and optimized: 9 mu L 1-undecanol microdrop exposed for 15 min floated on surface of a 10 mL water sample at 55 degrees C, stirred at 1200 rpm, low pH level and saturated salt conditions. Chromatographic problems associated with free phenols have been overcome by simultaneous in situ derivatization utilizing 40 mu L of acetic anhydride and 0.5% (w/v) K2CO3. Under the selected conditions, pre-concentration factor of 235-1174, limit of detection of 0.005-0.68 mu g/L (S/N=3) and linearity range of 0.02-300 mu g/L have been obtained. A reasonable repeatability (RSD <= 10.4%, n=5) with satisfactory linearity (0.9995 >= r(2) >= 0.9975) of results illustrated a good performance of the present method. The relative recovery of different natural water samples was higher than 84%.
机译:通过原位衍生化和使用新的液-液微萃取耦合GC-MS系统,可以实现水样品中8种酚类化合物的预浓缩和测定。已研究和优化了微萃取效率因素:将暴露于15分钟的9μL 1-十一醇微滴漂浮在55℃的10 mL水样品表面上,在1200 rpm,低pH值和饱和盐条件下搅拌。通过使用40μL乙酸酐和0.5%(w / v)K2CO3进行同时原位衍生化,可以克服与游离酚有关的色谱问题。在所选条件下,预浓缩系数为235-1174,检测极限为0.005-0.68μg / L(S / N = 3),线性范围为0.02-300μg / L。结果具有合理的线性(0.9995> = r(2)> = 0.9975)和合理的重复性(RSD <= 10.4%,n = 5),说明了本方法的良好性能。不同天然水样品的相对回收率高于84%。

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