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Continuous flow 2H/2H and 18O/16O analysis of water samples with dual inlet precision

MPG-Autoren
http://pubman.mpdl.mpg.de/cone/persons/resource/persons62380

Geilmann,  H.
Service Facility Stable Isotope/Gas Analytics, Dr. W. A. Brand, Max Planck Institute for Biogeochemistry, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons62528

Richter,  J.
Service Facility Stable Isotope/Gas Analytics, Dr. W. A. Brand, Max Planck Institute for Biogeochemistry, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons62603

Werner,  R. A.
Service Facility Stable Isotope/Gas Analytics, Dr. W. A. Brand, Max Planck Institute for Biogeochemistry, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons62345

Brand,  W. A.
Service Facility Stable Isotope/Gas Analytics, Dr. W. A. Brand, Max Planck Institute for Biogeochemistry, Max Planck Society;

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Zitation

Gehre, M., Geilmann, H., Richter, J., Werner, R. A., & Brand, W. A. (2004). Continuous flow 2H/2H and 18O/16O analysis of water samples with dual inlet precision. Rapid Communications in Mass Spectrometry, 18(22), 2650-2660.


Zitierlink: http://hdl.handle.net/11858/00-001M-0000-000E-D18E-7
Zusammenfassung
A method for isotope ratio analysis of water samples is described comprising an on-line high-temperature reduction technique in a helium carrier gas. Using a gas-tight syringe, injection of 0.5 to 1 muL sample is made through a heated septum into a glassy carbon reactor at temperatures in excess of 1300degreesC. More than 150 injections can be made per day and both isotope ratios of interest delta(2)H and 6180, can be measured with the same setup. The technique has the capability to transfer high-precision stable isotope ratio analysis of water samples from a specialized to a routine laboratory task compatible with other common techniques (automated injection for GC, LC, etc.). Experiments with an emphasis on the reactor design were made in two different laboratories using two different commercially available high-temperature elemental analyser (EA) systems. has been reduced to similar to1% and high precision of about 0.1parts per thousand for delta(18)O and <1parts per thousand for delta(2)H has been achieved by a redesign of the glassy carbon reactor and by redirecting the gas flow of the commercial TC/EA unit. With the modified reactor, the contact of water vapour with surfaces other than glassy carbon is avoided completely. The carrier gas is introduced at the bottom of the reactor thereby flushing the outer tube compartment of the tube-in-tube assembly before entering the active heart of the reactor. was obtained with a minor modification (electropolishing) of the injector metal sleeve. With this system, the temperature dependence of the reaction has been studied between 1100 and 1450degreesC. Complete yield and constant isotope ratio information has been observed only for temperatures above 1325degreesC. For temperatures above 1300degreesC the reactor produces an increasing amount of CO background from reaction of glass carbon with the ceramic tube. This limits the usable temperature to a maximum of 1450degreesC. Relevant gas permeation through the Al2O3 walls has not been detected up to 1600degreesC. Copyright (C) 2004 John Wiley Sons, Ltd. [References: 18]