Development of an In-Situ Mass Spectrometer for Stable Isotope Analysis

2003 ◽  
Author(s):  
R. T. Short ◽  
Gottfried P. Kibelka ◽  
Robert H. Byrne ◽  
David Hollander
2011 ◽  
Vol 44 (2) ◽  
pp. 429-432 ◽  
Author(s):  
Andrew J. Wall ◽  
Peter J. Heaney ◽  
Ryan Mathur ◽  
Jeffrey E. Post ◽  
Jonathan C. Hanson ◽  
...  

A non-metallic flow-through reaction cell is described, designed forin situtime-resolved X-ray diffraction coupled with stable isotope analysis. The experimental setup allows the correlation of Cu isotope fractionation with changes in crystal structure during copper sulfide dissolution. This flow-through cell can be applied to many classes of fluid–mineral reactions that involve dissolution or ion exchange.


2013 ◽  
Vol 47 (3) ◽  
pp. 1478-1486 ◽  
Author(s):  
Scott D. Wankel ◽  
Yi-wen Huang ◽  
Manish Gupta ◽  
Robert Provencal ◽  
J. Brian Leen ◽  
...  

Radiocarbon ◽  
2007 ◽  
Vol 49 (2) ◽  
pp. 233-244 ◽  
Author(s):  
Jesper Olsen ◽  
Jan Heinemeier ◽  
Klaus Bahner ◽  
Barry Graney ◽  
Andy Phillips

Accelerator mass spectrometry (AMS) radiocarbon measurements of organic samples require combustion to obtain CO2 for graphitization. Furthermore, determination of δ13C values is required in order to correct the 14C age due to carbon isotope fractionation effects. δ13C analysis is commonly carried out by stable isotope mass spectrometry because most applications demand high-precision δ13C values in addition to the requirements of 14C dating. A simplifying step is therefore to combine the combustion for stable isotope analysis with cryogenic trapping of CO2 for AMS graphite targets. Presented here is a simple CO2 trapping device based on a modified Gilson 220XL sampling (manifold) robot coupled to the inlet manifold system of a GV Instruments IsoPrime stable isotope mass spectrometer. The system is capable of batch combustion and analysis of up to 40 samples and is under full computer control by the mass spectrometer software. All trapping parameters such as flush time prior to trapping and total trap time are adjustable through the standard software user interface. A low 14C activity of background materials and high precision and accuracy of stable isotope analysis of carbon and nitrogen are demonstrated.


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