Adsorption and photocatalytic degradation of acetonitrile:: FT-IR investigation

被引:38
|
作者
Davit, P
Martra, G
Coluccia, S
Augugliaro, V
López, EG
Loddo, V
Marcì, G
Palmisano, L
Schiavello, M
机构
[1] Univ Turin, Dipartimento Chim IFM, I-10125 Turin, Italy
[2] Univ Palermo, Dipartimento ICPM, I-90128 Palermo, Italy
关键词
TiO2; acetonitrile; adsorption; photocatalysis; FF-IR investigation;
D O I
10.1016/S1381-1169(03)00354-6
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 degradation of acetonitrile was carried out in liquid-solid regime in a batch reactor by using two types of commercial TiO2 powders (Merck and Degussa P25) as photocatalysts. The concentration of acetonitrile and non-purgeable organic carbon (NPOC) were monitored. The initial rate of acetonitrile conversion was found higher on TiO2 Merck than on TiO2 P25. FT-IR spectroscopy was used to investigate the molecular features of the adsorption and photo-oxidation of acetonitrile on the two TiO2 powders in a fully surface hydrated form. Acetonitrile was found adsorbed on Ti4+ surface ions and hydroxyl groups for both types of TiO2. This interaction appeared fully reversible in the case of the Merck photocatalyst, whereas acetonitrile was more strongly stabilized on Ti4+ ions of TiO2 P25. Furthermore, the adsorption of CD3CN...Ti4+ on this type of photocatalyst resulted in the formation of acetamide-like species, because of the presence of nucleophilic surface O2- and hydroxyl groups. The formation of these species, strongly bound to the TiO2 surface and recalcitrant to the photo-oxidation, could result in the poisoning of a part of the photocatalytic sites of TiO2 P25, accounting for its lower initial acetonitrile conversion rate. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:693 / 701
页数:9
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