Operando DRIFTS study of the role of hydroxyls groups in trichloroethylene photo-oxidation over titanate and TiO2 nanostructures

被引:22
作者
Hernandez-Alonso, Maria D. [1 ]
Garcia-Rodriguez, Sergio [2 ]
Suarez, Silvia [1 ]
Portela, Raquel [1 ]
Sanchez, Benigno [1 ]
Coronado, Juan M. [3 ]
机构
[1] CIEMAT PSA, Madrid 28040, Spain
[2] CSIC, Inst Catalysis & Petroleochem, E-28049 Madrid, Spain
[3] IMDEA Energia, Thermochem Proc Unit, Madrid 28935, Spain
关键词
Photocatalysis; Operando; DRIFTS; Trichloroethylene; Titanate; Nanotubes; TiO2; Hydrothermal synthesis; Hydroxyls; PHOTOCATALYTIC OXIDATION; GAS-PHASE; DEGRADATION; SURFACE; AIR; PRODUCTS; SPECTROSCOPY; MECHANISM; WATER; FTIR;
D O I
10.1016/j.cattod.2012.01.029
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of the present research was to gain further insight into the differences of the trichloroethylene photodegradation routes when using TiO2 (Degussa P25) and protonated titanate nanotubes (H2Ti3O7). These last materials have structural hydroxyls that, along with the surface OH groups present in both photocatalysts, could mediate in the mineralization of the pollutant. In order to obtain a realistic view, an operando Diffuse Infrared Fourier Transform Spectroscopy (DRIFTS) approach has been adopted for surface analysis during the photocatalytic oxidation. The study revealed that the mineralization yield of trichloroethylene on the titanate nanotubes calcined at 300 degrees C was better than the one obtained with the benchmark photocatalyst Degussa P25. In particular, the synthesized nanotubes showed the selective removal of some specific hydroxyl groups, suggesting that their high density and, probably, the specific characteristics of their hydroxyl species can be responsible for the enhanced dechlorination photoactivity exhibited by these nanotubular structures. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
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