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Specificity of high resolution analysis of naphthenic acids in aqueous environmental matrices

机译:水性环境基质中环烷酸的高分辨率分析的特异性

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The determination of naphthenic acids to ultra-trace level is reported using liquid chromatography with quadrupole time-of-flight mass spectrometry detection (LC/QToF). The application of this method is in the rapid screening for low level oxygenated naphthenic acid species from potential oil sands process water (OSPW) spills and leakage from storage facilities into aquafers and waterways. During LC/QToF method optimization it was found to be essential to adjust sample pH to >10 prior to any sample container transfer or sub-sampling in order to avoid naphthenic acid losses. Under acidic conditions the loss of 04 species from AEOs was shown to range from 17% for earlier eluting C17 species, to 86% for a later C21 species. Despite application of high resolution mass spectrometry with a mass accuracy of 5 ppm, the potential for interference from environmental contaminants was demonstrated for recognized estrogenic contaminants, resin acids, and fatty acids. These contaminants occur in the environment from natural and human activity, for example fatty acids derived from the pulp and paper mill industry upstream of the Athabasca oil sands. In an effort to avoid potential false positive identifications at low NA concentration levels, formulae for Cn z-0 O2 fatty acids were excluded from total NA screening, it was further noted that OSPW-derived acid extractable organics (AEOs) and Merichem technical mixtures contained ~2.5% and ~1.8% respectively of compounds identified with formulae equivalent to both naphthenic and resin acids. The C20 resin acids, anticipated at higher levels in dystrophic water samples, were recommended for future exclusion. Similarly, estrogens, namely estrone, 17α-ethinylestradiol, and 17β-estradiol estrogens, were also identified as NA during screening but eluted at different retention times to the naphthenic acid homologs observed in NA technical mixtures. The potential for their erroneous inclusion in total naphthenic acid results is also discussed.
机译:使用液相色谱和四极杆飞行时间质谱检测(LC / QToF)报道了环烷酸超痕量测定。此方法的应用是从潜在的油砂工艺水(OSPW)泄漏和从存储设施泄漏到水族箱和水道中的低水平氧化环烷酸物种进行快速筛选。在LC / QToF方法优化过程中,发现必须进行任何样品容器转移或二次采样之前,将样品的pH调节至> 10,以避免环烷酸损失。在酸性条件下,从AEO中损失的04种物质显示范围从早期洗脱的C17物种的17%到后来的C21物种的86%。尽管应用了质量精度为5 ppm的高分辨率质谱仪,但对于公认的雌激素污染物,树脂酸和脂肪酸,仍证明了来自环境污染物的潜在干扰。这些污染物是由于自然和人类活动而在环境中产生的,例如源自阿萨巴斯卡油砂上游制浆造纸厂的脂肪酸。为了避免在低NA浓度水平下可能出现的假阳性识别结果,从总NA筛选中排除了Cn z-0 O2脂肪酸的配方,进一步注意到OSPW衍生的酸可萃取有机物(AEO)和Merichem技术混合物分别用相当于环烷酸和树脂酸的分子式鉴定的化合物约为〜2.5%和〜1.8%。建议将营养不良水样品中的C20树脂酸含量提高,以备将来排除。同样,雌激素,即雌酮,17α-炔雌醇和17β-雌二醇,在筛选过程中也被鉴定为NA,但在与NA技术混合物中观察到的环烷酸同系物的保留时间不同。还讨论了将其错误地包含在总环烷酸中的可能性。

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