H2S photodegradation by TiO2/M-MCM-41 (M = Cr or Ce): Deactivation and by-product generation under UV-A and visible light

被引:57
|
作者
Portela, Raquel [1 ]
Canela, Maria C. [2 ]
Sanchez, Benigno [1 ]
Marques, Fabielle C. [2 ]
Stumbo, Alexandre M. [2 ]
Tessinari, Ronan F. [2 ]
Coronado, Juan M. [1 ]
Suarez, Silvia [1 ]
机构
[1] CIEMAT, PSA Environm Applicat Solar Radiat, E-28040 Madrid, Spain
[2] Univ Estadual N Fluminen, CCT, Lab Ciencias Quim, Campos dos Goytacazes, RJ, Brazil
关键词
H2S; MCM-41; Cr; Ce; Mesoporous; Photocatalysis; Visible light; Deactivation;
D O I
10.1016/j.apcatb.2008.05.020
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
M-MCM-41 molecular sieves (M = Ce or Cr) were prepared by a hydrothermal method and impregnated with TiO2. The materials were characterized by XRD, N-2 adsorption-desorption, DRS and XPS. Their potential application to photooxidize H2S in a wet gas stream was tested in a continuous flow reactor operating at a flow rate of 110 mL min(-1) at 50% relative humidity and using 30 ppm(v) of the pollutant. The photocatalytic efficiency using UV-A and visible light was compared to the activity of TiO2/MCM-41 without heteroatoms incorporated into the MCM-41 structure. It was found that the incorporation of Ce did not improve the performance of TiO2/MCM-41, but Cr-containing samples presented higher initial efficiency and were able to photooxidize H2S without formation of SO2 as a by-product, in contrast to the other prepared samples and to Degussa P-25 TiO2. Moreover, no other gaseous by-product was detected. The isomorphic incorporation of Cr into the structure of MCM-41 followed by TiO2 incorporation produced photocatalysts that presented good adsorption capacity and were much more active under visible light than under UV-Iight. This performance represents an important advantage for solar applications. Their photoactivity depended on the concentration of chromium; the highest efficiency was attained with samples with a Si/Cr ratio of 50. Finally, deactivation was observed as a consequence of sulfate accumulation on the surface of the catalyst and reduction of Cr6+. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:643 / 650
页数:8
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