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Sorption of Nuclear Waste Components by Layered Hydrazinium Titanate: a Straightforward Route to Durable Ceramic Forms

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Abstract

Layered hydrazinium titanate LHT-9, (N2H5)1/2Ti1.87O4 is a new nanohybrid material related to lepidocrocite-type titanates. Unique combination of ion exchange, reductive properties, surface activity due to Bransted acid sites and occurrence of surface titanyl groups allows exploring LHT-9 for simultaneous uptake of almost all components of liquid nuclear wastes. LHT-9 irreversibly removes technetium, molybdenum, palladium and selenium from their aqueous solutions by specific mechanism of reductive adsorption. For removal of cesium, strontium, transition elements, actinides and lanthanides LHT-9 provides mechanisms of ion exchange and surface complexation. Products of adsorption are nanocrystalline and homogeneous powders loaded with 5 to 15 wt. % of radionuclides and non-radioactive elements. LHT-9 can be applied as ready-to-use precursor for one-step synthesis of durable titanate ceramic waste forms similar to SYNROC. An essential advantage of LHT-9 in comparison with other titanate sorbents (monosodium titanate and peroxo-titanate materials) is the absence of Na in its composition that permits arbitrary tailoring of sorbent properties by simple pre-treatment with the desired elements. Results on sorption of americium, cesium, strontium and lanthanides by LHT-9 are discussed.

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Acknowledgments

This research was supported in part by a grant from the Deutsche Forschungsgemeinschaft (DE 412/39-1), by the V.G. Khlopin Radium Institute (KRI), Russian Federal Grant-in-Aid contracts 02.740.11.0326 and 16.513.11.3033, and internal budget grant of St. Petersburg State University 3.37.84.2011. L.K. acknowledges financial support by the Deutsche Forschungsgemeinschaft in the frame of the Heisenberg Program.

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Britvin, S.N., Korneyko, Y.I., Burakov, B.E. et al. Sorption of Nuclear Waste Components by Layered Hydrazinium Titanate: a Straightforward Route to Durable Ceramic Forms. MRS Online Proceedings Library 1475, 191–196 (2012). https://doi.org/10.1557/opl.2012.575

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  • DOI: https://doi.org/10.1557/opl.2012.575

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