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Fast and Precise Method for Pb Isotope Ratio Determination in Complex Matrices using GC-MC-ICPMS: Application to Crude Oil, Kerogen, and Asphaltene Samples

机译:使用GC-MS-ICP MS快速,精确地测定复杂基质中的Pb同位素比:在原油,干酪根和沥青质样品中的应用

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摘要

A new method to determine Pb isotope ratio without ion-exchange-matrix separation is proposed. After acid digestion, Pb was ethylated to Et_(4)Pb, separated from the digested solution (black shale, asphaltene, crude oil and kerogen) by extraction in isooctane, and then injected into a gas chromatograph coupled to a multicollector inductively coupled plasma mass spectrometer. Seven isotopes (~(202)Hg, ~(203)Tl, ~(204)Pb, ~(205)Tl, ~(206)Pb, ~(207)Pb, ~(208)Pb) were monitored simultaneously with peak duration of 23 s. GC elution was operated under wet plasma conditions where a thallium standard solution was introduced to the mass spectrometer for mass bias correction. The total time of the procedure (sample preparation and analysis, after acid digestion) was reduced by a factor of 15 compared to conventional-continuous sample introduction. Data treatment was carried out using the linear regression slope method. Mass bias was corrected using the double correction method (first thallium normalization followed by classical bracketing). For the ~(208/206)Pb and ~(207/206)Pb ratios, precision (2RSD_(EXT), n = 21) was 49 and 69 ppm, and the bias between experimental results and reference values was better than 0.0033 and 0.0007 ‰, when injecting 1.2 ng of ethylated Pb SRM NIST 981 solution. Results obtained by this method were validated by comparison with those obtained via conventional-continuous sample introduction. The applicability of this approach was demonstrated with the analysis of black shale, asphaltene, crude oil and kerogen samples.
机译:提出了一种无需离子交换-基质分离即可确定Pb同位素比的新方法。酸消解后,将Pb乙基化为Et_(4)Pb,通过在异辛烷中萃取从消解的溶液(黑页岩,沥青质,原油和干酪根)中分离出来,然后注入连接有多收集器电感耦合血浆物质的气相色谱仪中光谱仪。同时监测七个同位素(〜(202)Hg,〜(203)Tl,〜(204)Pb,〜(205)Tl,〜(206)Pb,〜(207)Pb,〜(208)Pb)持续时间23 s。 GC洗脱是在湿血浆条件下进行的,其中将was标准溶液引入质谱仪进行质量偏差校正。与常规连续进样相比,该过程的总时间(样品制备和分析,酸消解后)减少了15倍。使用线性回归斜率方法进行数据处理。使用双重校正方法(首先进行normal归一化,然后进行经典括号法)校正质量偏倚。对于〜(208/206)Pb和〜(207/206)Pb的比率,精度(2RSD_(EXT),n = 21)为49和69 ppm,实验结果与参考值之间的偏差优于0.0033和注射1.2 ng乙基化Pb SRM NIST 981溶液时为0.0007‰。通过与通过常规连续样品引入获得的结果进行比较,验证了通过该方法获得的结果。通过分析黑页岩,沥青质,原油和干酪根样品证明了该方法的适用性。

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