Coupled Si and O isotope measurements of meteoritic material by laser fluorination isotope ratio mass spectrometry

2019 ◽  
Vol 54 (8) ◽  
pp. 667-675
Author(s):  
Patrick J. A. Hill ◽  
Neil R. Banerjee ◽  
Arshad Ali ◽  
Iffat Jabeen ◽  
Gordon R. Osinski ◽  
...  

2002 ◽  
Vol 35 ◽  
pp. 125-130 ◽  
Author(s):  
Radboud van Trigt ◽  
Harro A. J. Meijer ◽  
Arny E. Sveinbjörnsdóttir ◽  
Sigfús J. Johnsen ◽  
Erik R.Th. Kerstel

AbstractWe report on the first application of a new technique in ice-core research, based on direct absorption infrared laser spectrometry (LS), for measuring 2H, 17Oand 18O isotope ratios. the data are used to calculate the deuterium excess d (defined as δ2H– 8δ18O) for a section of the Dye-3 (south Greenland) deep ice core around the Bølling transition (14 500 BP). the precision of LS is slightly better than that of most traditional methods for deuterium, but not for the oxygen isotopes. the ability to measure δ17O is new and is used here to improve the precision of the δ18O determination. Still, the final precision for δ18O remains inferior to traditional isotope ratio mass spectrometry (IRMS). Therefore, deuterium excess was calculated from a combination of the LS and IRMS isotope determinations.



2013 ◽  
Vol 726-731 ◽  
pp. 1346-1349 ◽  
Author(s):  
Chun Ying Xu ◽  
Yu Zhong Li ◽  
Qiao Zhen Li ◽  
Yi Wei Dong ◽  
Fu Li Fang ◽  
...  

A modified denitrifier method on Tracegas-isotope ratio mass spectrometry (IRMS) was developed to determine the nitrogen and oxygen isotopic compositions of nitrate (NO3-) in water samples. The protocol presented in our previous publication was modified in several aspects. Then, the incubation time, amount of NO3-sample, and effect of trapping time in the Tracegas system were analyzed using the standard reference USGS34. Both δ15N and δ18O values demonstrated accurate and reproducible at incubation times exceeding 12 h or overnight as well as added 0.2 μg to 0.4 μg NO3--N samples. Our data also showed that 100 s for trapping time in Tracegas system was adequate to achieve accurate and reproducible results. Finally, the δ15N and δ18O values of nitrate in animal wastewater were measured using this method. The results indicate that the denitrifier method can be used widely for tracing nitrate sources and controlling nitrate contamination in China.







2014 ◽  
Vol 28 (13) ◽  
pp. 1413-1425 ◽  
Author(s):  
Bin Hu ◽  
Jens Radke ◽  
Hans-Jürgen Schlüter ◽  
Frank Torsten Heine ◽  
Liping Zhou ◽  
...  


Author(s):  
Xing Wang ◽  
Henk G. Jansen ◽  
Haico Duin ◽  
Harro A. J. Meijer

AbstractThere are two officially approved methods for stable isotope analysis for wine authentication. One describes δ18O measurements of the wine water using Isotope Ratio Mass Spectrometry (IRMS), and the other one uses Deuterium-Nuclear Magnetic Resonance (2H-NMR) to measure the deuterium of the wine ethanol. Recently, off-axis integrated cavity output (laser) spectroscopy (OA-ICOS) has become an easier alternative to quantify wine water isotopes, thanks to the spectral contaminant identifier (SCI). We utilized an OA-ICOS analyser with SCI to measure the δ18O and δ2H of water in 27 wine samples without any pre-treatment. The OA-ICOS results reveal a wealth of information about the growth conditions of the wines, which shows the advantages to extend the official δ18O wine water method by δ2H that is obtained easily from OA-ICOS. We also performed high-temperature pyrolysis and chromium reduction combined with IRMS measurements to illustrate the “whole wine” isotope ratios. The δ18O results of OA-ICOS and IRMS show non-significant differences, but the δ2H results of both methods differ much more. As the δ2H difference between these two methods is mainly caused by ethanol, we investigated the possibility to deduce deuterium of wine ethanol from this difference. The results present large uncertainties and deviate from the obtained 2H-NMR results. The deviation is caused by the other constituents in the wine, and the uncertainty is due to the limited precision of the SCI-based correction, which need to improve to obtain the 2H values of ethanol as alternative for the 2H-NMR method.



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