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A novel tool for stable nitrogen isotope analysis in aqueous samples.
Federherr, E; Kupka, H J; Cerli, C; Kalbitz, K; Dunsbach, R; Loos, A; de Reus, M; Lange, L; Panetta, R J; Schmidt, T C.
Afiliação
  • Federherr E; Research and Innovation, Elementar Analysensysteme GmbH, Donaustr. 7, 63452, Hanau, Germany.
  • Kupka HJ; Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, 45141, Essen, Germany.
  • Cerli C; Research and Innovation, Elementar Analysensysteme GmbH, Donaustr. 7, 63452, Hanau, Germany.
  • Kalbitz K; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Science Park 904, 1098, XH, Amsterdam, The Netherlands.
  • Dunsbach R; Institute of Soil Science and Site Ecology, Technical University of Dresden, Pienner Str. 21, 01737, Tharandt, Germany.
  • Loos A; Research and Innovation, Taunus Instruments GmbH, Berlinerstr. 2, 61267, Neu-Anspach, Germany.
  • de Reus M; Research and Innovation, Elementar Analysensysteme GmbH, Donaustr. 7, 63452, Hanau, Germany.
  • Lange L; Research and Innovation, Elementar Analysensysteme GmbH, Donaustr. 7, 63452, Hanau, Germany.
  • Panetta RJ; Research and Innovation, Elementar Analysensysteme GmbH, Donaustr. 7, 63452, Hanau, Germany.
  • Schmidt TC; Research and Innovation, Isoprime Ltd, Cheadle Hulme, SK8 6PT, UK.
Rapid Commun Mass Spectrom ; 30(23): 2537-2544, 2016 Dec 15.
Article em En | MEDLINE | ID: mdl-27619634
ABSTRACT
RATIONALE Bulk stable isotope analysis (BSIA) of dissolved matter (e.g. dissolved organic carbon, total nitrogen bound (TNb ), etc.) is of particular importance since this pool is a prime conduit in the cycling of N and C. Studying the two elemental pools is of importance, as transformation and transport processes of N and C are inextricably linked in all biologically mediated systems. No system able to analyze natural abundance stable carbon and nitrogen isotope composition in aqueous samples (without offline sample preparation) and simultaneously has been reported so far. Extension of the high-temperature combustion (HTC) system, to be capable of measuring TNb stable nitrogen isotope composition, is described in this study.

METHODS:

To extend the TOC analyzer to be capable of measuring TNb , modifications from the HTC high-performance liquid chromatography/isotope ratio mass spectrometry (HPLC/IRMS) interface were implemented and expanded. A reduction reactor for conversion of NOx into N2 was implemented into the new developed system. The extension addresses mainly the development of the focusing unit for nitrogen and a degassing device for online separation of TNb from molecular nitrogen (N2 ) prior to injection.

RESULTS:

The proof of principle of the system was demonstrated with different compound solutions. In this initial testing, the δ15 NAIR-N2 values of the tested compounds were determined with precision and trueness of typically ≤0.5‰. Good results (u ≤ 0.5‰) could be achieved down to a TNb concentration of 40 mgN/L and acceptable results (u ≤ 1.0‰) down to 5 mgN/L. In addition, the development resulted in the first system reported to be suitable for simultaneous and direct δ13 C and δ15 N BSIA of aqueous samples.

CONCLUSIONS:

The development resulted in the first system shown to be suitable for both δ13 C and δ15 N direct BSIA in aqueous samples. This system could open up new possibilities in SIA-based research fields. Copyright © 2016 John Wiley & Sons, Ltd.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article