Articles & Issues
- Language
- English
- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
-
Received October 28, 2002
Accepted November 20, 2002
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright © KIChE. All rights reserved.
All issues
Effect of Calcination Temperature on the Characteristics of SO4(2-)/TiO2 Catalysts for the Reduction of NO by NH3
Department of Chemical Engineering/School of Environmental Science & Engineering, Pohang University of Science and Technology (POSTECH), San 31 Hyoja-Dong, Pohang 790-784, Korea 1Department of Chemical Engineering, Kyungil University, 33 Buhori, Hayang, Kyungsan 712-701, Korea 2Korea Electric Power Research Institute (KEPRI), 103-16 Moonji-Dong, Daejeon 305-308, Korea
isnam@postech.ac.kr
Korean Journal of Chemical Engineering, March 2003, 20(2), 273-278(6), 10.1007/BF02697240
Download PDF
Abstract
The catalytic activity of sulfated titania (ST) calcined at a variety of temperatures has been investigated for selective catalytic reduction (SCR) of NO by NH3. The NO removal activity of ST catalyst mainly depends on its sulfur content, indicating critical role of sulfur species on the surface of TiO2. The role of sulfur is mainly the formation of acid sites on the catalyst surface. The presence of both Brønsted and Lewis acid sites on the surface of sulfated titania has been identified by IR study with the adsorption of NH3 and pyridine on ST. The reduction of the intensity_x000D_
of IR bands representing Brønsted acid sites is more pronounced than that revealing Lewis acid sites as the calcination temperature increases. It has been further clarified by IR study of ST500 catalyst evacuated at a variety of temperatures. The NO removal activity also decreases with the increase of the catalyst calcination temperature. It simply reveals that Brønsted acid sites induced by sulfate on the catalyst surface are primarily responsible for the enhancement of catalytic activity of ST catalyst containing sulfur for NO reduction by NH3.
References
Alemany LJ, Lietti L, Ferlazzo N, Forzatti P, Busca G, Giamello E, Bregani F, J. Catal., 155(1), 117 (1995)
Amiridis MD, Wachs IE, Deo G, Jehng JM, Kim DS, J. Catal., 161(1), 247 (1996)
Busca G, Saussey H, Saur O, Lavalley JC, Lorenzelli V, Appl. Catal., 14, 245 (1985)
Chen LP, Yang RT, J. Catal., 139, 277 (1993)
Choi EY, Nam IS, Kim YG, J. Catal., 161(2), 597 (1996)
Choo ST, Lee YG, Nam IS, Ham SW, Lee JB, Appl. Catal. A: Gen., 200(1-2), 177 (2000)
Choo ST, Koh JY, Nam IS, Ham SW, Lee JB, Kim KY, HWAHAK KONGHAK, 38(5), 597 (2000)
Ebitani K, Tanaka T, Hattori H, Appl. Catal. A: Gen., 102(2), 102 (1993)
Ferwerda R, Mass JH, Duijneveldt FB, J. Mol. Catal. A-Chem., 104, 319 (1996)
Ham SW, Nam IS, Kim YG, Korean J. Chem. Eng., 17(3), 318 (2000)
Ham SW, Nam IS, Catalysis, 16, 236 (2002)
Hino M, Arata K, J. Chem. Soc.-Chem. Commun., 851 (1980)
Jung SM, Grange P, Catal. Today, 59(3-4), 305 (2000)
Jung SM, Grange P, Appl. Catal. B: Environ., 27(1), 11 (2000)
Kustov LM, Kazansky VB, Figueras F, Tichit D, J. Catal., 150(1), 143 (1994)
Navarrete J, Lopez T, Gomez R, Figueras F, Langmuir, 12(18), 4385 (1996)
Nortier P, Fourre P, Mohamed Saad AB, Saur O, Lavalley JC, Appl. Catal., 61, 141 (1990)
Orsenigo C, Lietti L, Tronconi E, Forzatti P, Bregani F, Ind. Eng. Chem. Res., 37(6), 2350 (1998)
Pasel J, Speer V, Albrecht C, Richter F, Papp H, Appl. Catal. B: Environ., 25(2-3), 105 (2000)
Primet M, Pichat P, Mathieu M, J. Phys. Chem., 75(9), 1216 (1971)
Sayari A, Dicko A, J. Catal., 145(2), 561 (1994)
Song XM, Sayari A, Catal. Rev.-Sci. Eng., 38(3), 329 (1996)
Tanabe K, "Solid Acids and Bases Their Catalytic Properties," Kodansha, Tokyo (1970)
Ward JW, "Infrared Studies of Zeolite Surfaces and Surface Reactions," ZEolite Chemistry and Catalysis, Rabo, J.A., eds., American Chemical Society, Washington D.C. (1976)
Yamaguchi T, Appl. Catal., 61(1), 1 (1990)
Amiridis MD, Wachs IE, Deo G, Jehng JM, Kim DS, J. Catal., 161(1), 247 (1996)
Busca G, Saussey H, Saur O, Lavalley JC, Lorenzelli V, Appl. Catal., 14, 245 (1985)
Chen LP, Yang RT, J. Catal., 139, 277 (1993)
Choi EY, Nam IS, Kim YG, J. Catal., 161(2), 597 (1996)
Choo ST, Lee YG, Nam IS, Ham SW, Lee JB, Appl. Catal. A: Gen., 200(1-2), 177 (2000)
Choo ST, Koh JY, Nam IS, Ham SW, Lee JB, Kim KY, HWAHAK KONGHAK, 38(5), 597 (2000)
Ebitani K, Tanaka T, Hattori H, Appl. Catal. A: Gen., 102(2), 102 (1993)
Ferwerda R, Mass JH, Duijneveldt FB, J. Mol. Catal. A-Chem., 104, 319 (1996)
Ham SW, Nam IS, Kim YG, Korean J. Chem. Eng., 17(3), 318 (2000)
Ham SW, Nam IS, Catalysis, 16, 236 (2002)
Hino M, Arata K, J. Chem. Soc.-Chem. Commun., 851 (1980)
Jung SM, Grange P, Catal. Today, 59(3-4), 305 (2000)
Jung SM, Grange P, Appl. Catal. B: Environ., 27(1), 11 (2000)
Kustov LM, Kazansky VB, Figueras F, Tichit D, J. Catal., 150(1), 143 (1994)
Navarrete J, Lopez T, Gomez R, Figueras F, Langmuir, 12(18), 4385 (1996)
Nortier P, Fourre P, Mohamed Saad AB, Saur O, Lavalley JC, Appl. Catal., 61, 141 (1990)
Orsenigo C, Lietti L, Tronconi E, Forzatti P, Bregani F, Ind. Eng. Chem. Res., 37(6), 2350 (1998)
Pasel J, Speer V, Albrecht C, Richter F, Papp H, Appl. Catal. B: Environ., 25(2-3), 105 (2000)
Primet M, Pichat P, Mathieu M, J. Phys. Chem., 75(9), 1216 (1971)
Sayari A, Dicko A, J. Catal., 145(2), 561 (1994)
Song XM, Sayari A, Catal. Rev.-Sci. Eng., 38(3), 329 (1996)
Tanabe K, "Solid Acids and Bases Their Catalytic Properties," Kodansha, Tokyo (1970)
Ward JW, "Infrared Studies of Zeolite Surfaces and Surface Reactions," ZEolite Chemistry and Catalysis, Rabo, J.A., eds., American Chemical Society, Washington D.C. (1976)
Yamaguchi T, Appl. Catal., 61(1), 1 (1990)