Treatment of chemical warfare agents by zero-valent iron nanoparticles and ferrate(VI)/(III) composite
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22119195
DOI
10.1016/j.jhazmat.2011.10.094
PII: S0304-3894(11)01348-3
Knihovny.cz E-resources
- MeSH
- Chemical Warfare Agents chemistry MeSH
- Water Pollutants, Chemical chemistry MeSH
- Cholinesterase Inhibitors chemistry MeSH
- Water Purification methods MeSH
- X-Ray Diffraction MeSH
- Microscopy, Electron, Scanning MeSH
- Nanoparticles chemistry ultrastructure MeSH
- Organothiophosphorus Compounds chemistry MeSH
- Oxidation-Reduction MeSH
- Powder Diffraction MeSH
- Soman chemistry MeSH
- Mustard Gas chemistry MeSH
- Iron chemistry MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Chemical Warfare Agents MeSH
- Water Pollutants, Chemical MeSH
- Cholinesterase Inhibitors MeSH
- ferrate ion MeSH Browser
- Organothiophosphorus Compounds MeSH
- Soman MeSH
- VX MeSH Browser
- Mustard Gas MeSH
- Iron MeSH
Nanoscale zero-valent iron (nZVI) particles and a composite containing a mixture of ferrate(VI) and ferrate(III) were prepared by thermal procedures. The phase compositions, valence states of iron, and particle sizes of iron-bearing compounds were determined by combination of X-ray powder diffraction, Mössbauer spectroscopy and scanning electron microscopy. The applicability of these environmentally friendly iron based materials in treatment of chemical warfare agents (CWAs) has been tested with three representative compounds, sulfur mustard (bis(2-chlorethyl) sulfide, HD), soman ((3,3'-imethylbutan-2-yl)-methylphosphonofluoridate, GD), and O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothiolate (VX). Zero-valent iron, even in the nanodimensional state, had a sluggish reactivity with CWAs, which was also observed in low degrees of CWAs degradation. On the contrary, ferrate(VI)/(III) composite exhibited a high reactivity and complete degradations of CWAs were accomplished. Under the studied conditions, the estimated first-order rate constants (≈ 10(-2)s(-1)) with the ferrate(VI)/(III) composite were several orders of magnitude higher than those of spontaneous hydrolysis of CWAs (10(-8)-10(-6)s(-1)). The results demonstrated that the oxidative technology based on application of ferrate(VI) is very promising to decontaminate CWAs.
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