Regenerable ceria-based SOx traps for sulfur removal in lean exhausts

被引:44
作者
Kylhammar, Lisa [1 ]
Carlsson, Per-Anders [1 ]
Ingelsten, Hanna Harelind [1 ]
Gronbeck, Henrik [1 ]
Skoglundh, Magnus [1 ]
机构
[1] Chalmers, Competence Ctr Catalysis, SE-41296 Gothenburg, Sweden
关键词
FTIR spectroscopy; Storage mechanism; CeO2; Pt; Sulfur oxide;
D O I
10.1016/j.apcatb.2008.04.003
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
Bare and Pt-containing CeO2, Al2O3:MgO mixed oxide and Al2O3 have been investigated as potential regenerable sulfur oxides (SOx) traps. The samples were evaluated by lean SOx adsorption and temperature programmed desorption using synthetic gas compositions. In addition, combined DRIFT spectroscopy and mass spectrometry were employed to obtain mechanistic information on the adsorption of SOx. The results suggest Pt/CeO2 as promising SOx trap material owing to a high storage capacity at 250 degrees C in combination with efficient release above 600 degrees C. The presence of Pt is generally found to enhance the lean SOx storage capacity at 250 degrees C for CeO2-based samples. Lean SO2 adsorption on CeO2 is found to proceed via the formation of surface and bulk sulfates, where the latter is formed more rapidly for the Pt-containing CeO2. sample. Ceria samples pre-exposed to high amounts of SO2 at 250 and 400 degrees C show lower SOx storage capacity and higher SOx release as compared to fresh samples. This indicates that under the conditions used in this study, a part of the storage sites on CeO2 are non-regenerable. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:268 / 276
页数:9
相关论文
共 25 条
[1]   Sulfur deactivation of NOx storage catalysts:: influence of exposure conditions and noble metal [J].
Amberntsson, A ;
Skoglundh, M ;
Ljungström, S ;
Fridell, E .
JOURNAL OF CATALYSIS, 2003, 217 (02) :253-263
[2]  
Amberntsson A, 1999, STUD SURF SCI CATAL, V126, P317
[3]   Influence of platinum on ceria sulfation [J].
Bazin, P ;
Saur, O ;
Lavalley, JC ;
Blanchard, G ;
Visciglio, V ;
Touret, O .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1997, 13 (3-4) :265-274
[4]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[5]   NOx storage-reduction catalysts based on hydrotalcite -: Effect of Cu in promoting resistance to deactivation [J].
Centi, G ;
Fornasari, G ;
Gobbi, C ;
Livi, M ;
Trifirò, F ;
Vaccari, A .
CATALYSIS TODAY, 2002, 73 (3-4) :287-296
[6]   Sulfate formation on SOx trapping materials studied by cu and SK-edge XAFS [J].
Dathe, H ;
Jentys, A ;
Lercher, JA .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2005, 7 (06) :1283-1292
[7]   Sulfur deactivation of Pt/SiO2, Pt/BaO/Al2O3, and BaO/Al2O3 NOx storage catalysts:: Influence of SO2 exposure conditions [J].
Dawody, J ;
Skoglundh, M ;
Olsson, L ;
Fridell, E .
JOURNAL OF CATALYSIS, 2005, 234 (01) :206-218
[8]   Role of Pt-precursor on the performance of Pt/BaCO3Al2O3-NOx storage catalysts [J].
Dawody, J ;
Skoglundh, M ;
Wall, S ;
Fridell, E .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 225 (02) :259-269
[9]   Role of the Mg/Al atomic ratio in hydrotalcite-based catalysts for NOx storage/reduction [J].
Fornasari, G ;
Glöckler, R ;
Livi, M ;
Vaccari, A .
APPLIED CLAY SCIENCE, 2005, 29 (3-4) :258-266
[10]   NOx storage in barium-containing catalysts [J].
Fridell, E ;
Skoglundh, M ;
Westerberg, B ;
Johansson, S ;
Smedler, G .
JOURNAL OF CATALYSIS, 1999, 183 (02) :196-209