Title of article :
Study on the effective decontamination and hydrolysis of sulfur mustard agent simulant using tenorite (CuO) nanoparticles as a destructive catalyst
Author/Authors :
صادقي، ميثم نويسنده دانشجوي كارشناس ارشد سنجش و اندازه گيري SADEGHI, M , يكتا، سينا نويسنده Department of Chemistry, Islamic Azad University of Qaemshahr., P.O. BOX 163, Qaemshahr, Iran Yekta , Sina , حسيني، ميرحسن نويسنده Department of Chemistry, University of Imam Hussein Comprehensive, P.O. BOX 995-16765, Tehran, Iran Hosseini, Mirhassan , تقي زاده، محمد جواد نويسنده Department of Chemistry, Imam Hossein University, P.O. BOX 995-16765 Tehran, Iran Taghizadeh, Mohammad Javad
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2015
Pages :
12
From page :
125
To page :
136
Abstract :
In the present study, tenorite (CuO) nanoparticles have been assayed for their catalytic properties. The decontamination reaction of chloro ethyl ethyl sulfide (CEES) as an surrogate of sulfur mustard have been accomplished on the surface of CuO NPs with different weight ratios at ambient temperature and monitored by Gas chromatography equipped with Flame ionization detector (GC-FID) and Gas chromatography coupled with a mass spectroscopy (GC-MS). CuO NPs were successfully synthesized via precipitation method in the absence and presence of polyvinylpyrrolydone (PVP) and copper (??) nitrate as the precursors. PVP was used as a capping agent to control and reduce the agglomeration of the nanoparticles. The synthesized CuO NPs were characterized by Scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and X-ray diffraction (XRD) techniques. The GC analysis results revealed that the decontamination of CEES occurred in n-hexane solvent with the weight ratio of 1:40 (CEES: CuO NPs) after 12 h with more than 90% yield. The hydrolysis product such as hydroxyl ethyl ethyl sulfide (HEES) was also identified by GC-MS analysis.
Journal title :
Iranian Chemical Communication
Journal title :
Iranian Chemical Communication
Record number :
2395269
Link To Document :
بازگشت