Development of new method of δ13C measurement for trace hydrocarbons in natural gas using solid phase micro-extraction coupled to gas chromatography isotope ratio mass spectrometry

被引:40
作者
Li, Zhongping [1 ,2 ,3 ]
Wang, Xibin [1 ]
Li, Liwu [1 ]
Zhang, Mingjie [2 ,3 ]
Tao, Mingxin [4 ]
Xing, Lantian [1 ]
Cao, Chunhui [1 ]
Xia, Yanqing [1 ]
机构
[1] Chinese Acad Sci, Inst Geol & Geophys, Gansu Prov Key Lab Petr Resources Res, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Sch Earth Sci, Lanzhou 730000, Peoples R China
[3] Lanzhou Univ, Gansu Key Lab Mineral Resources Western China, Lanzhou 730000, Peoples R China
[4] Beijing Normal Univ, Coll Resources Sci & Technol, Beijing 100875, Peoples R China
基金
美国国家科学基金会;
关键词
Carbon isotope; Solid-phase micro extraction; Gas chromatography; Isotope ratio mass spectrometry; Trace hydrocarbons; Natural gas; LIGHT-HYDROCARBONS; MICROEXTRACTION; BASIN; VOLATILES; OILS;
D O I
10.1016/j.chroma.2014.10.089
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Compound specific isotope analysis (CSIA) of normal-level hydrocarbons (C-1-C-4) in natural gas is often successfully used in natural gas origin identification and classification, but little progress so far has been made for trace level hydrocarbons (C-5-C-14) in natural gas. In this study, we developed a method for rapid analysis of carbon isotopic ratios for trace hydrocarbons in natural gas samples. This method can be described as a combined approach characterized by solid phase micro-extraction (SPME) technique coupled to gas chromatography isotope ratio mass spectrometry (GC/IRMS). In this study, the CAR-PDMS fiber was chosen as the SPME adsorptive material after comparative experiments with other four fibers, and the parameters, including equilibration time, extraction temperature and desorption time, for efficient extraction of trace hydrocarbons were systematically optimized. The results showed the carbon isotopic fractionation was not observed as a function of equilibration time and extraction temperature. And the delta C-13 signatures determined by SPME-GC/IRMS were in good agreement with the known delta C-13 values of C-5-C-14 measured by GC-IRMS, and the accuracy is generally within +/- 0.5 parts per thousand. Five natural gas samples were analyzed using this method, and the delta C-13 values for C-5-C-14 components were obtained with satisfied repeatability. The SPME-GC/IRMS approach fitted with CAR-PDMS fiber is well suited for the preconcentration of trace hydrocarbons and provides so far the most reliable carbon isotopic analysis for trace compounds in natural gas. Published by Elsevier B.V.
引用
收藏
页码:228 / 235
页数:8
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