Photo-degradation of yperite over V, Fe and Mn-doped titania- silica photocatalysts

被引:21
作者
Neatu, Stefan [1 ]
Parvulescu, Vasile I. [1 ]
Epure, Gabriel [2 ]
Preda, Emilia [2 ]
Somoghi, Vasile [2 ]
Damin, Alessandro [3 ,4 ]
Bordiga, Silvia [3 ,4 ]
Zecchina, Adriano [3 ,4 ]
机构
[1] Univ Bucharest, Fac Chem, Dept Chem Technol & Catalysis, Bucharest 030018, Romania
[2] Chem Ctr Def NBC & Ecol, Bucharest 041309, Romania
[3] Univ Turin, Dept Chem, IFM, I-10125 Turin, Italy
[4] NIS Ctr Excellence, I-10125 Turin, Italy
关键词
D O I
10.1039/b810200g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photocatalytic decomposition of yperite (bis(2-chloroethyl) sulfide), a chemical warfare agent, was achieved by using titania-silica catalysts doped with several transition metal ions. The preparation of these catalysts was achieved by impregnation of a titania-silica mixed oxide previously synthesized using a sol-gel route with salts of the doping elements (vanadium, iron, manganese). The above catalysts were characterized using several spectroscopic techniques: FTIR, Raman, DR-UV-Vis, and XPS. The band gap energy was measured for each photocatalytic system. The reaction was carried out in two different types of reactors, i.e. naturally aerated and a closed quartz tube aerated under a constant flow, and using two types of irradiation, UV-Vis and Vis. The investigated systems proved to be extremely active, leading to an almost complete degradation of yperite in 2 h of irradiation. An excellent correlation between the photocatalytic performances and the band gap has been found. Based on the characterization data and on the temporal evolution of the reaction products, a reaction mechanism has been suggested. This mechanism considers two distinct pathways for the decomposition of yperite, namely the C-S bond cleavage and the S oxidation.
引用
收藏
页码:6562 / 6570
页数:9
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