English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
 
 
DownloadE-Mail
  Improved isotope ratio measurement performance in liquid chromatography/isotope ratio mass spectrometry by removing excess oxygen

Hettmann, E., Brand, W. A., & Gleixner, G. (2007). Improved isotope ratio measurement performance in liquid chromatography/isotope ratio mass spectrometry by removing excess oxygen. Rapid Communications in Mass Spectrometry, 21(24), 4135-4141. doi:10.1002/rcm.3304.

Item is

Files

show Files
hide Files
:
BGC1236.pdf (Publisher version), 233KB
 
File Permalink:
-
Name:
BGC1236.pdf
Description:
-
OA-Status:
Visibility:
Restricted (Max Planck Institute for Biogeochemistry, MJBK; )
MIME-Type / Checksum:
application/octet-stream
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-

Locators

show

Creators

show
hide
 Creators:
Hettmann, E.1, Author           
Brand, W. A.2, Author           
Gleixner, G.1, Author           
Affiliations:
1Molecular Biogeochemistry Group, Dr. G. Gleixner, Department Biogeochemical Processes, Prof. E.-D. Schulze, Max Planck Institute for Biogeochemistry, Max Planck Society, ou_1497773              
2Service Facility Stable Isotope/Gas Analytics, Dr. W. A. Brand, Max Planck Institute for Biogeochemistry, Max Planck Society, ou_1497772              

Content

show
hide
Free keywords: -
 Abstract: A low dead volume oxygen scrubbing system was introduced in a commercially available liquid chromatography/isotope ratio mass spectrometry (LC/IRMS) interface to enhance the analytical capability of the system. In the LC/IRMS interface carbon from organic samples is converted into CO2 inside the mobile phase by wet chemical oxidation using peroxodisulfate (Na2S2O8). After passing the hot reaction zone, surplus oxygen (O-2) remains dissolved in the liquid phase. Both CO2 and O-2 diffuse through a transfer membrane into the helium carrier and are transferred to the mass spectrometer. The presence of O-2 in the ion source may have detrimental effects on measurement accuracy and precision as well as on filament lifetime. As a remedy, a new on-line O-2-removing device has been incorporated into the system. The new O-2 scrubber consists of two parallel hot copper reduction reactors (0.8 mm i.d., active length 120mm) and a switch-over valve between them. One reactor is regenerated using He/H-2 while the other is actively scavenging O-2 from the gas stream. The capacity of each reduction reactor, expressed as usage time, is between 40 and 50 min. This is sufficient for a single LC run for sugars and organic acids. A further increase of the reduction capacity is accompanied by a peak broadening of about 100%. After switching to a freshly reduced reactor the oxygen background and the delta C-13 values of the reference gas need up to 500 s to stabilize. For repeated injections the delta C-13 values of sucrose remain constant (+/- 0.1 parts per thousand) for about 3000 s. The long-term stability for measurements of sucrose was 0.11 parts per thousand without the reduction oven and improved slightly to 0.08 parts per thousand with the reduction oven. The filament lifetime improved by more than 600%, thereby improving the long-term system stability and analytical efficiency. In addition the costs per analysis were reduced considerably.

Details

show
hide
Language(s):
 Dates: 2007
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1002/rcm.3304
Other: BGC1236
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Rapid Communications in Mass Spectrometry
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: New York, NY : John Wiley & Sons
Pages: - Volume / Issue: 21 (24) Sequence Number: - Start / End Page: 4135 - 4141 Identifier: CoNE: https://pure.mpg.de/cone/journals/resource/954925574961
ISSN: 0951-4198