Published December 15, 2006 | Version v1
Journal article

Trapping of radiolytic hydrogen by amorphous cobalt oxysulfide

  • 1. Institut de Recherches sur la Catalyse, CNRS UPR 5401, 2 Av. A. Einstein, 69626 Villeurbanne (France)
  • 2. Institut de Physique Nucleaire de Lyon, 4 rue E. Fermi, 69622 Villeurbanne (France)
  • 3. Ecole Nationale Superieure des Mines de Saint-Etienne, LPMG, CNRS UMR 5148, Centre SPIN, 158 cours Fauriel, 42023 Saint-Etienne (France)
  • 4. Institut de Radioprotection et de Surete Nucleaire, BP. 17, 92262 Fontenay aux Roses (France)

Description

Hydrogen production from the radiolysis of liquid and gaseous hydrocarbons was studied in the presence of several transition metal sulfides. Cobalt oxysulfide obtained by aqueous precipitation was the most efficient admixture to decrease radiolytic production of hydrogen by pure hydrocarbons or mixtures of saturated and unsaturated hydrocarbons. Cobalt oxysulfide was characterized by XRD, scanning and transmission microscopy, and IR spectroscopy. It seems to be amorphous compound with the impurities of lamellar Co(OH)2 phase. The organic phases were analysed before and after irradiation by γ-rays or protons in order to elucidate the origin of the effect. It has been shown that the solid does not change the composition neither the amount of the organic radiolysis products, neither in liquid nor in gas phase experiments. Therefore the presence of solid does not influence any radiolysis processes in the organics. Amorphous cobalt oxysulfide acts essentially as a trap of hydrogen, being able to absorb considerable amounts of H2 (up to 0.5 mol H2/at. Co). The study of the solid-gas interaction showed that slow reaction of cobalt oxysulfide with hydrogen occurs at ambient conditions independently of the irradiation of the system

Additional details

Identifiers

DOI
10.1016/j.jnucmat.2006.09.002;
PII
S0022-3115(06)00471-5;

Publishing Information

Journal Title
Journal of Nuclear Materials
Journal Volume
359
Journal Issue
3
Journal Page Range
p. 238-246
ISSN
0022-3115
CODEN
JNUMAM

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.