Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2010Studies on the Preparation of Small 14C Samples with an RGA and 13C-Enriched Materialcitations

Places of action

Chart of shared publication
Wild, Eva Maria
1 / 3 shared
Steier, Peter
1 / 5 shared
Liebl, Jakob
1 / 4 shared
Kutschera, Walter
1 / 3 shared
Golser, Robin
1 / 4 shared
Ortiz, Roswitha Avalos
1 / 1 shared
Chart of publication period
2010

Co-Authors (by relevance)

  • Wild, Eva Maria
  • Steier, Peter
  • Liebl, Jakob
  • Kutschera, Walter
  • Golser, Robin
  • Ortiz, Roswitha Avalos
OrganizationsLocationPeople

article

Studies on the Preparation of Small 14C Samples with an RGA and 13C-Enriched Material

  • Wild, Eva Maria
  • Steier, Peter
  • Liebl, Jakob
  • Kutschera, Walter
  • Golser, Robin
  • Handle, Florian
  • Ortiz, Roswitha Avalos
Abstract

The minimum size of radiocarbon samples for which reliable results can be obtained in an accelerator mass spectrometry (AMS) measurement is in many cases limited by carbon contamination introduced during sample preparation (i.e. all physical and chemical steps to which samples were subjected, starting from sampling). Efforts to reduce the sample size limit down to a few ƒÝg carbon require comprehensive systematic investigations to assess the amount of contamination and the process yields. We are introducing additional methods to speed up this process and to obtain more reliable results. A residual gas analyzer (RGA) is used to study combustion and graphitization reactions. We could optimize the reaction process at small CO2 pressures and identify detrimental side reactions. Knowing the composition of the residual gas in a graphitization process allows a reliable judgment on the completeness of the reaction. Further, we use isotopically enriched 13C („d98% 13C) as a test material to determine contamination levels. This offers significant advantages: 1) The measurement of 12C/13C in CO2 is possible on-line with the RGA, which significantly reduces turnaround times compared to AMS measurements; 2) Both the reaction yield and the amount of contamination can be determined from a single test sample. The first applications of isotopically enriched 13C and the RGA have revealed that our prototype setup has room for improvements via better hardware; however, significant improvements of our sample processing procedures were achieved, eventually arriving at an overall contamination level of 0.12 to 0.15 ƒÝg C during sample preparation (i.e. freeze-drying, combustion, and graphitization) of ƒÝg-sized samples in aqueous solution, with above 50% yield

Topics
  • impedance spectroscopy
  • Carbon
  • combustion
  • additive manufacturing
  • spectrometry
  • drying
  • Accelerator mass spectrometry