4.6 Article

NOx abatement from stationary emission sources by photo-assisted SCR: Lab-scale to pilot-scale studies

Journal

APPLIED CATALYSIS A-GENERAL
Volume 523, Issue -, Pages 294-303

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcata.2016.06.020

Keywords

NOx abatement; Photo-assisted SCR; Photocatalyst; Desulfurization; Pilot-scale; Lab-scale

Funding

  1. Ministry of Science and Technology, Taiwan [NSC 103-2923-E-002-002-MY3]
  2. National Centre for Research and Development, Poland [DKO/PL-TW1/2/2013]

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In developing a higher activity for NOx abatement from stationary emission sources, photo-assisted elective catalytic reduction (photo-SCR) was systematically investigated over TiO2 supported on a spherical alpha-Al2O3/gamma-Al2O3. The formation of NO2 was virtually suppressed in the reaction temperature range of 110-200 degrees C. The NOx removal efficiencies of TiO2/gamma-Al2O3 photocatalyst at 120 degrees C for real flue gas (in pilot-scale photoreactor) and simulated flue gas (in lab-scale photoreactor) were 68-75% and 43.5%, respectively, in the presence of reducing reagent (C4H10). SEM and XPS techniques revealed that sulfur temporarily occupied the active sites of the photocatalyst, causing deactivation. Spent TiO2/gamma-Al2O3 photocatalyst was regenerated via desulfurization by either air or hydrogen at 400-500 degrees C. The effects of regeneration temperature and regeneration time on the photocatalytic activity are methodically investigated, demonstrating that using hydrogen at 500 degrees C in 1 h could completely regenerate the spent photocatalyst. (C) 2016 Elsevier B.V. All rights reserved.

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