Online high-precision δ2H and δ18O analysis in water by pyrolysis

被引:2
|
作者
Lu, Feng H. [1 ]
机构
[1] US EPA, Robert S Kerr Environm Res Ctr, Stable Isotope Lab, Ada, OK 74820 USA
关键词
RATIO MASS-SPECTROMETRY;
D O I
10.1002/rcm.4232
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method for online simultaneous delta H-2 and delta O-18 analysis in water by high-temperature conversion is presented. Water is injected by using a syringe into a high-temperature carbon reactor and converted into H-2 and CO, which are separated by gas chromatography (GC) and carried by helium to the isotope ratio mass spectrometer for hydrogen and oxygen isotope analysis. A series of experiments was conducted to evaluate several issues such as sample size, temperature and memory effects. The delta H-2 and delta O-18 values in multiple water standards changed consistently as the reactor temperature increased from 1150 to 1480 degrees C. The delta O-18 in water can be measured at a lower temperature (e.g. 1150 degrees C) although the precision was relatively poor at temperatures <1300 degrees C. Memory effects exist for delta H-2 and delta O-18 between two waters, and can be reduced (to <1%) with proper measures. The injection of different amounts of water may affect the isotope ratio results. For example, in contrast to small injections (100 nL or less) from small syringes (e.g. 1.2 mu L), large injections (1 mu L or more) from larger syringes (e.g. 10 mu L) with dilution produced asymmetric peaks and shifts of isotope ratios, e.g. 4 parts per thousand for delta H-2 and 0.4 parts per thousand for delta O-18, probably resulting from isotope fractionation during dilution via the ConFlo interface. This method can be used to analyze nanoliter samples of water (e.g. 30 nL) with good precision of 0.5 parts per thousand for delta H-2 and 0.1 parts per thousand for delta O-18. This is important for geosciences; for instance, fluid inclusions in ancient minerals may be analyzed for delta H-2 and delta O-18 to help understand the formation environments. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:3144 / 3150
页数:7
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