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Pure Appl. Chem., 2002, Vol. 74, No. 2, pp. 187-316

http://dx.doi.org/10.1351/pac200274020187

ORGANIC AND BIOMOLECULAR CHEMISTRY DIVISION
IUPAC COMMITTEE ON CHEMICAL WEAPON DESTRUCTION TECHNOLOGIES
WORKING PARTY ON EVALUATION OF CHEMICAL WEAPON DESTRUCTION TECHNOLOGIES

Critical evaluation of proven chemical weapon destruction technologies (IUPAC Technical Report)

Graham S. Pearson1* and Richard S. Magee2

1 Department of Peace Studies, University of Bradford, Bradford, West Yorkshire BD7 1DP, UK
2 Carmagen Engineering, Inc., 4 West Main Street, Rockaway, NJ 07866, USA

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  • Singh Ravindra, Gutch P.K., Mazumder Avik: N, N-Dichlorourethane: An Efficient Decontaminating Reagent for Sulfur Mustard, a Chemical Warfare Agent. Ind. Eng. Chem. Res. 2013, 52, 4689. <http://dx.doi.org/10.1021/ie301991q>
  • Barbara Radke, Linda Jewell, Piketh Stuart, Namieśnik Jacek: Arsenic-based warfare agents: production, use and destruction. Critical Reviews in Environmental Science and Technology 2013, 130828234456003. <http://dx.doi.org/10.1080/10643389.2013.782170>
  • Negishi T., Matsunaga Y., Kobayashi Y., Hirano S., Tashiro T.: Developmental Subchronic Exposure to Diphenylarsinic Acid Induced Increased Exploratory Behavior, Impaired Learning Behavior, and Decreased Cerebellar Glutathione Concentration in Rats. Toxicological Sciences 2013, 136, 478. <http://dx.doi.org/10.1093/toxsci/kft200>
  • Gutch Pranav K., Mazumder Avik: N,N-Dichlorovaleramide: An Efficient Decontaminating Reagent for Sulfur Mustard. Industrial Eng Chem Res 2012, 51, 5830. <http://dx.doi.org/10.1021/ie201811v>
  • Negishi Takayuki, Takahashi Masaki, Matsunaga Yuki, Hirano Seishiro, Tashiro Tomoko: Diphenylarsinic Acid Increased the Synthesis and Release of Neuroactive and Vasoactive Peptides in Rat Cerebellar Astrocytes. Journal of Neuropathology & Experimental Neurology 2012, 71, 468. <http://dx.doi.org/10.1097/NEN.0b013e3182561327>
  • Kim Kibong, Tsay Olga G., Atwood David A., Churchill David G.: Destruction and Detection of Chemical Warfare Agents. Chemistry Review 2011, 111, 5345. <http://dx.doi.org/10.1021/cr100193y>
  • Valyashko V. M., Urusova M. A.: Heterogenization of supercritical fluids and nonvariant critical equilibria in ternary systems with one volatile component (for water-salt systems as examples). Russ J Phys Chem B 2010, 4, 1130. <http://dx.doi.org/10.1134/S1990793110070134>
  • Tafesse Fikru, Eguzozie Kennedy: Efficient hydrolysis of 4-nitrophenylphosphate catalyzed by copper bipyridyl in microemulsions. Ecotoxicological and Environmental Safety 2009, 72, 954. <http://dx.doi.org/10.1016/j.ecoenv.2008.01.010>
  • Kato Koichi, Mizoi Mutsumi, An Yan, Nakano Masayuki, Wanibuchi Hideki, Endo Ginji, Endo Yoko, Hoshino Mikio, Okada Shoji, Yamanaka Kenzo: Oral administration of diphenylarsinic acid, a degradation product of chemical warfare agents, induces oxidative and nitrosative stress in cerebellar Purkinje cells. Life Sci Oxford 2007, 81, 1518. <http://dx.doi.org/10.1016/j.lfs.2007.09.030>
  • Sciaini Germán, Marceca Ernesto, Fernández-Prini Roberto: Solubility of crystalline alkali metal iodides in supercritical ammonia. J Sup Fluids 2005, 35, 106. <http://dx.doi.org/10.1016/j.supflu.2004.12.013>
  • Tafesse Fikru: Hydrolysis of 4‐Nitrophenyl Phosphate in Microemulsions Assisted by Polymetallic Complexes: A Bio‐mimetic Model for Decontamination of Organophosphate Pollutants. Synthesis & Reactivity in Inorg Metal-Org & Nano-Metal Chem 2005, 35, 645. <http://dx.doi.org/10.1080/15533170500225524>
  • Ishii Kazuhiro, Tamaoka Akira, Otsuka Fujio, Iwasaki Nobuaki, Shin Kenji, Matsui Akira, Endo Ginji, Kumagai Yoshito, Ishii Tetsuro, Shoji Shin'ichi: Diphenylarsinic acid poisoning from chemical weapons in Kamisu, Japan. Ann Neurol 2004, 56, 741. <http://dx.doi.org/10.1002/ana.20290>
  • Brown R Stan, Neverov Alexei A, Tsang Josephine SW, Gibson Graham TT, Montoya-Pelaez Pedro J: 2004 Bader Award Lecture Metal-ion-catalyzed acyl and phosphoryl transfer reactions to alcohols: La3+-promoted alcoholysis of activated amides, carboxylate esters, and neutral organophosphorus esters. Can J Chem 2004, 82, 1791. <http://dx.doi.org/10.1139/v04-167>