Study on detoxification property of alkaline-modified MoO42--H2O2 decontaminants against PhSMe under subzero environment

Shaohua Wei; Hongpeng Zhang; Haiyan Zhu; Lianyuan Wang; Jing Liang; Zhenxing Cheng

doi:10.1051/e3sconf/202126702061

All issues

Volume 267 (2021)

E3S Web Conf., 267 (2021) 02061

References

Open Access

Issue		E3S Web Conf. Volume 267, 2021 7^th International Conference on Energy Science and Chemical Engineering (ICESCE 2021)


Article Number		02061
Number of page(s)		5
Section		Environmental Chemistry Research and Chemical Preparation Process
DOI		https://doi.org/10.1051/e3sconf/202126702061
Published online		04 June 2021

Zhao S P, Xi H L, Zuo Y J, Han S T, Zhu Y B, Li Z G, et al. (2019) Rapid activation of basic hydrogen peroxide -by borate and efficient destruction of toxic industrial chemicals (TICs) and chemical warfare agents (CWAs). J. Hazardous Materials, 367: 91–98 [Google Scholar]
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Bennett D A, Yao H, Richardson D E. (2001) Mechanism of sulfide oxidations by peroxymonocarbonate. J. Inorganic Chemistry, 40 (13): 2996–3001 [Google Scholar]
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[1] Zhao S P, Xi H L, Zuo Y J, Han S T, Zhu Y B, Li Z G, et al. (2019) Rapid activation of basic hydrogen peroxide -by borate and efficient destruction of toxic industrial chemicals (TICs) and chemical warfare agents (CWAs). J. Hazardous Materials, 367: 91–98 [Google Scholar]

[2] Kim K O, Tsay G, Atwood D A, and Churchill D G. (2011) Destruction and Detection of Chemical Warfare Agents Chem Rev, 111: 5345–5403 [Google Scholar]

[3] Richardt A, Blum M M. (2008) Decontamination of Warfare Agents, WILEY-VCH Verlag GmbH & Co.KGaA, Weinheim [Google Scholar]

[4] Tadros M E, Tucker M D. (2003) U.S. 6566574 [Google Scholar]

[5] Wagner G W, Procell L R, Henderson V D, Sorrick D C, Hess Z A, Gehring D G, Brickhouse M D. (2004) Decon Green. R. U.S. Army Edgewood Chemical Biological Center [Google Scholar]

[6] Bunton C A, Gillitt N D. (2002) Oxidation of thioanisole by peroxomolybdate ions: direct oxygen transfer from tetrperoxomolybdate ion. J. Physical Organic Chemistry, 15(1): 29–35 [Google Scholar]

[7] Vakhitova L N, Matvienko K V, Taran N A, et al. (2011) Nucleophilic oxidizing systems based on hydrogen peroxide for decomposition of ecotoxicants. J. Russ J Org Chem, 47 (7): 965–973. [Google Scholar]

[8] Fakhraian H, Valizadeh F. (2010) Activation of hydrogen peroxide via bicarbonate, sulfate, phosphate and urea in the oxidation of methyl phenyl sulfide. J. Mol Catal A: Chem, 333(1/2): 69-72. [Google Scholar]

[9] Zhao S P, Xi H L, Zuo Y J, et al. (2015) Oxidation Kinetics and Products of Methyl Phenyl Sulfide, a Sulfur Mustard Simulant by Sodium Molybdate Catalyzed Hydrogen Peroxide Solutio. J. Molecular Catalysis, 29: 45–51. [Google Scholar]

[10] Vakhitova L N, Skrypka A V, Savelova V A, et al. (2005) Kinetics of the oxidation of methyl phenyl sulfide by hydrogen peroxide in the presense of hydrocarbonate an ion. J. Theoretical and Experimental Chemistry, 41(2): 98–104 [Google Scholar]

[11] Bennett D A, Yao H, Richardson D E. (2001) Mechanism of sulfide oxidations by peroxymonocarbonate. J. Inorganic Chemistry, 40 (13): 2996–3001 [Google Scholar]

[12] Rappoport Z. (2006) The Chemistry of Peroxides. M. John Wiley Sons Ltd, 2: 1–92 [Google Scholar]