Cerium oxide for the destruction of chemical warfare agents: A comparison of synthetic routes
Creators
- 1. Faculty of the Environment, University of Jan Evangelista Purkyně, Králova Výšina 7, 400 96 Ústí nad Labem (Czech Republic)
- 2. Institute of Inorganic Chemistry AS CR v.v.i., 25068 Řež (Czech Republic)
- 3. Faculty of Sciences, University of Jan Evangelista Purkyně, České Mládeže 8, 400 96 Ústí nad Labem (Czech Republic)
- 4. Military Research Institute, Veslařská 230, 637 00 Brno (Czech Republic)
Description
Highlights: • Four synthetic routes were compared to prepare the nanoceria-based reactive sorbents. • The sorbents prepared by homogeneous hydrolysis destroy efficiently the soman and VX nerve agents. • Toxic organophosphates are converted to less-dangerous products completely within a few minutes. • Surface non-stoichiometry and −OH groups promote the destruction by the SN2 mechanism. - Abstract: Four different synthetic routes were used to prepare active forms of cerium oxide that are capable of destroying toxic organophosphates: a sol–gel process (via a citrate precursor), homogeneous hydrolysis and a precipitation/calcination procedure (via carbonate and oxalate precursors). The samples prepared via homogeneous hydrolysis with urea and the samples prepared via precipitation with ammonium bicarbonate (with subsequent calcination at 500 °C in both cases) exhibited the highest degradation efficiencies towards the extremely dangerous nerve agents soman (O-pinacolyl methylphosphonofluoridate) and VX (O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothioate) and the organophosphate pesticide parathion methyl. These samples were able to destroy more than 90% of the toxic compounds in less than 10 min. The high degradation efficiency of cerium oxide is related to its complex surface chemistry (presence of surface −OH groups and surface non-stoichiometry) and to its nanocrystalline nature, which promotes the formation of crystal defects on which the decomposition of organophosphates proceeds through a nucleophilic substitution mechanism that is not dissimilar to the mechanism of enzymatic hydrolysis of organic phosphates by phosphotriesterase.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2015.10.069Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2015.10.069;
- PII
- S0304-3894(15)30195-3;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 304
- Journal Page Range
- p. 259-268
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48046681
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CERIUM OXIDES; CHEMICAL WARFARE AGENTS; COMPARATIVE EVALUATIONS; CRYSTAL DEFECTS; ENZYMATIC HYDROLYSIS; OXIDATION; PHOSPHATES; SOL-GEL PROCESS; SURFACES; TOXICITY
- Descriptors DEC
- CERIUM COMPOUNDS; CHALCOGENIDES; CHEMICAL REACTIONS; CRYSTAL STRUCTURE; DECOMPOSITION; EVALUATION; HYDROLYSIS; LYSIS; OXIDES; OXYGEN COMPOUNDS; PHOSPHORUS COMPOUNDS; RARE EARTH COMPOUNDS; SOLVOLYSIS; WEAPONS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.