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Dive into the research topics where Hans-Jürgen Schlüter is active.

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Featured researches published by Hans-Jürgen Schlüter.


Rapid Communications in Mass Spectrometry | 2014

A modified procedure for gas‐source isotope ratio mass spectrometry: the long‐integration dual‐inlet (LIDI) methodology and implications for clumped isotope measurements

Bin Hu; Jens Radke; Hans-Jürgen Schlüter; Frank Torsten Heine; Liping Zhou; Stefano M. Bernasconi

RATIONALE High-precision stable isotope measurements in gas-source isotope ratio mass spectrometry are generally carried out by repeated comparison of the composition of an unknown sample with that of a working gas (WG) through a dual-inlet (DI). Due to the established DI protocols, however, most of the sample gas is wasted rather than measured, which is a major problem when sample size is limited. Here we propose a new methodology allowing the measurement of a much larger portion of the available sample. METHODS We tested a new measurement protocol, the long-integration dual-inlet (LIDI) method, which consists of a single measurement of the sample for 200 to 600 seconds followed by a single measurement of the WG. The isotope ratios of the sample are calculated by comparison of the beam ratios of the WG and sample at equivalent intensities of the major ion beam. RESULTS Three isotopically very different CO2 samples were analyzed. The LIDI measurements of large samples (50 to 100 µmol of CO2) measured at quasi-constant beam sizes, and of small samples (1.5 to 2 µmol of CO2) measured in micro-volume mode, generated results that are indistinguishable from the standard DI measurements for carbon, oxygen and clumped isotope compositions. The external precision of Δ47 using the LIDI protocol (~±0.007‰) is similar to that of the state of the art DI measurements. CONCLUSIONS For traditional and clumped isotope measurements of CO2, the LIDI protocol allows the measurement of a much larger portion of the sample gas rather than only ~20% of it. In addition, the sample can be measured at higher signal intensity and for longer time, allowing the measurement of smaller samples while preserving precision. We suggest that other gases commonly used for stable isotope measurements with gas-source mass spectrometry would also benefit from this new protocol.


Archive | 2008

DEVICE FOR THE ANALYSIS OF ISOTOPE RATIOS

Deike Hatscher; Andreas Hilkert; Hans-Jürgen Schlüter; Alexander Duhr; Michael Krummen; Johannes Schwieters


Archive | 2007

Method and device for the analysis of isotope ratios

Deike Hatscher; Andreas Hilkert; Hans-Jürgen Schlüter; Alexander Duhr; Michael Krummen; Johannes Schwieters


Archive | 2008

Sample Excitation Apparatus and Method for Spectroscopic Analysis

Hans-Jürgen Schlüter; Robert Malek


Archive | 2006

METHOD AND APPARATUS FOR PROVIDING A SUBSTANCE FOR THE ANALYSIS OF ISOTOPE RATIOS

Michael Krummen; Hans-Jürgen Schlüter


Archive | 2014

GAS INLET SYSTEM FOR ISOTOPE RATIO ANALYSER AND METHOD OF DETERMINING AN ISOTOPE RATIO

Eric Wapelhorst; Hans-Jürgen Schlüter; Oliver Kracht; Johannes Schwieters; Michael Krummen


Archive | 2008

Einrichtung zur Bereitstellung von Gasen, insbesondere für die Isotopenverhältnisanalyse

Michael Krummen; Hans-Jürgen Schlüter


Archive | 2007

Device for feeding gases to an analysis instrument

Hans-Jürgen Schlüter; Alexander Duhr; Deiko Hatscher; Andreas Hilkert; Michael Krummen; Johannes Schwieters


Archive | 2016

GAS INLET SYSTEM FOR ISOTOPE RATIO SPECTROMETER

Hans-Jürgen Schlüter; Johannes Schwieters; Eric Wapelhorst; Michael Krummen


Archive | 2016

Verfahren und vorrichtung zur vorkonzentration einer gasförmigen probe A method and apparatus for pre-concentration of a gaseous sample

Johannes Schwieters; Michael Krummen; Hans-Jürgen Schlüter; Oliver Kracht

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Alexander Duhr

Thermo Fisher Scientific

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Deike Hatscher

Thermo Fisher Scientific

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Oliver Kracht

Thermo Fisher Scientific

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Dirk Wohlers

Thermo Fisher Scientific

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Horst Sudholz

Thermo Fisher Scientific

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Jens Radke

Thermo Fisher Scientific

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