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

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 i...

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Detalhes bibliográficos
Autores: Hernández-Alonso, María D., García Rodríguez, Sergio, Suárez Gil, Silvia, Portela, Raquel, Sánchez, Benigno, Coronado, Juan M.
Tipo de documento: artigo
Data de publicação:2013
País:España
Recursos:Consejo Superior de Investigaciones Científicas (CSIC)
Repositório:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/163175
Acesso em linha:http://hdl.handle.net/10261/163175
Access Level:Acceso aberto
Palavra-chave:Photocatalysis
Operando
DRIFTS
Trichloroethylene
Titanate
Nanotubes
TiO2
Hydrothermal synthesis
Hydroxyls
Descrição
Resumo: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 °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.