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Analysis of Nitrosamines in Wastewater: Exploring the Trace Level Quantification Capabilities of a Hybrid Linear Ion Trap/Orbitrap Mass Spectrometer

机译:废水中亚硝胺的分析:探索混合线性离子阱/轨道阱质谱仪的痕量水平定量能力

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A method was developed to determine nine N-nitrosamines in wastewater on the basis of solid-phase extraction and liquid chromatography mass spectrometry using a linear ion trap-orbitrap hybrid instrument at high mass resolution. Analytes and five deuterated internal standards were preconcentrated by solid-phase extraction. Positive electrospray ionization resulted in protonated molecular ions of all nitrosamines. One to three product ions were formed by collision-induced dissociation or higher energy C-trap dissociation. The signal intensity of the product ions differed up to a factor of 3 between the two techniques. The molecular ions were usually used for quantification, because of the better sensitivity, and the product ions for confirmation. An actual mass resolving power of 25 000-40 000 ensured a sufficient selectivity to distinguish all molecular and product ions from interfering background ions. Only for N-nitrosomorpholine was a coeluting isobaric molecular ion detected in wastewater samples, which, however, formed different product ions. The mass accuracy was between -12 ppm at m/z 55 and 0 ppm at m/z 205 and did not change for more than 5 ppm over a sample sequence of 20 h analysis time. The optimized method allowed quantifying nine N-nitrosamines in drinking water and wastewater samples down to method detection limits of 0.3-3.9 ng/L at instrumental detection limits of 2-14 pg on column. Recoveries over the whole method were between 75 and 125percent for six compounds, but considerably lower for three compounds, probably due to strong matrix effects causing a signal suppression of up to 95percent in wastewater samples. N-Nitrosodimethylamine and N-nitrosomorpholine were the most abundant compounds (3-22 ng/L) in samples from two wastewater treatment plants, another four nitrosamines (N-nitrosopyrrolidone, -piperidine, -diethylamine, and -dibutylamine) were also detected. Our study demonstrates that the LTQ Orbitrap is a powerful instrument to quantify low molecular weight compounds at the picogram level in complex matrixes with both a high sensitivity and selectivity.
机译:在固相萃取和液相色谱质谱联用的基础上,使用线性离子阱-轨道阱混合仪器以高分辨率对废水中的九种亚硝胺进行了测定。通过固相萃取对分析物和五种氘代内标进行预浓缩。正电喷雾电离产生所有亚硝胺的质子化分子离子。通过碰撞诱导的离解或更高能的C陷阱离解形成一到三个产物离子。在这两种技术之间,产物离子的信号强度相差3倍。由于具有更高的灵敏度,分子离子通常用于定量分析,而产物离子则用于确认。实际的质量分辨能力为25 000-40 000确保了足够的选择性,以区分所有分子离子和产物离子与干扰本底离子。仅对于N-亚硝基吗啉,才在废水样品中检测到共洗脱的同量异位分子离子,但是形成了不同的产物离子。质量精度在m / z 55下为-12 ppm至在m / z 205下为0 ppm,并且在20小时分析时间内的样品序列中变化不超过5 ppm。优化的方法允许定量分析饮用水和废水样品中的九种N-亚硝胺,方法中检测限为0.3-3.9 ng / L,仪器上的仪器检测限为2-14 pg。整个方法中六种化合物的回收率在75%至125%之间,而三种化合物的回收率则低得多,这可能是由于强大的基质效应导致废水样品中的信号抑制高达95%。在两个废水处理厂的样品中,N-亚硝基二甲胺和N-亚硝基吗啉是最丰富的化合物(3-22 ng / L),另外还检测到另外四个亚硝胺(N-亚硝基吡咯烷酮,-哌啶,-二乙胺和-二丁胺)。我们的研究表明,LTQ Orbitrap是一种功能强大的仪器,能够以高灵敏度和高选择性在皮克级定量分析复杂基质中的低分子量化合物。

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