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|Title:||Photocatalytic conversion of NO using TiO₂-NH₃catalysts in ambient air environment|
Hou, M. F.
|Source:||Applied catalysis B: Environmental, 30 Dec. 2004, v. 54, no. 4, p. 275-283.|
|Abstract:||Photocatalytic conversion of nitric oxide (NO) in ambient air was studied in a continuous-flow photoreactor system at room temperature using different TiO₂catalysts prepared with different titanium precursors of Ti(SO₄)₂, TiOSO₄, and Ti(O-Bu)₄by either a moderate-temperature hydrothermal process or a hydrothermal reflux process. The physicochemical properties of the prepared catalysts were characterized by XRD, BET, FTIR, and SEM. Analytical results showed that the crystallinity, morphology, nitrogen adsorption–desorption isotherms, specific surface area, and pore size distribution of catalysts were significantly affected by the precursors and hydrothermal processes, but the crystal structure and crystal size of catalysts were not significantly influenced. The NO conversion experiments demonstrated that the TiO₂catalysts prepared by the moderate-temperature hydrothermal process without ammonia pretreatment could effectively reduce NO to different low levels, in which the catalysts with longer aging time of more than 12 h performed better than the catalysts with shorter aging time. However, it was found that the NO₂concentration in outlet gas was gradually increased with extension of an experimental period. Two TiO₂catalysts (TOSO-NH₃and TOB-NH₃) prepared by the hydrothermal reflux process with ammonia pretreatment demonstrated a very good performance in NO conversion and also maintained a low level of NO₂concentration in outlet gas. This study indicated that using the TiO₂catalysts modified with ammonia pretreatment in photocatalytic reaction could provide a good approach to effectively eliminate the accumulation of NO₂product from NO oxidation in the system and to achieve a sustainable process, which may be applicable for NO elimination in ambient air environment.|
|Rights:||Applied Catalysis B: Environmental © 2004 Elsevier B. V. The journal web site is located at http://www.sciencedirect.com.|
|Appears in Collections:||CEE Journal/Magazine Articles|
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