1. Introduction
Tritium and radiocarbon are currently the two main radionuclides that might be discharged in water bodies by the industry and particularly by heavy-water reactors, such as CANDU reactors. Tritium widely integrates into the water cycle and follows the water mass dynamics but it may also be integrated for long term into the organic pool, persisting in aquatic environment according to the recycling rates of organic matter (Eyrolle-Boyer et al., 2015). The experimental data indicated a time lag between concentrations of tritium in water and sediments, reflecting non-equilibrium attributed to the specific dynamics of tissue free water tritium (TFWT as HTO) and organically bound tritium (OBT) forms: TFWT follows the transfer of water while OBT depends on process linked to organic matter (biomass production, degradation and recycling). Tritium persistence through its OBT forms in biomass and aquatic systems may have a major impact on environmental compartments submitted to chronic releases (Eyrolle-Boyer et al., 2014), due to its significant radiotoxicity and contribution to the total dose (Galeriu et. al., 2010; UNSCEAR, 2000). Current measurement of organically bound tritium (OBT) from sediment using liquid scintillation counting (LSC) implies first of all conversion of organic matter in liquid water. In order to convert sediment organic matter to water it is necessary to perform a total oxidation process, which most commonly can be made through wet oxidation (Ware and Allot, 1999; Environment Agency, 2005) or combustion using different type of catalytic furnaces (Cossonnet et. al., 2009; Daillant et. al., 2004; Eyrolle-Boyer et al., 2014; Fournier et. al. 2002; Morris, 2006; Vichot et. al. 2005,) or the devices called oxidizers (Kim et. al., 2013).