Ammonia formation over supported platinum and palladium catalysts

被引:30
|
作者
Adams, Emma Catherine [1 ]
Skoglundh, Magnus [1 ]
Folic, Milica [2 ]
Bendixen, Eva Charlotte [1 ,2 ]
Gabrielsson, Par [2 ]
Carlsson, Per-Anders [1 ]
机构
[1] Chalmers Univ Technol, Competence Ctr Catalysis, SE-42196 Gothenburg, Sweden
[2] Haldor Topsoe Res Labs, DK-2800 Lyngby, Denmark
关键词
Catalytic exhaust aftertreatment; Passive-SCR; NO(x)reduction; In situ DRIFT spectroscopy; NH3; formation; LEAN NOX REDUCTION; NOBLE-METAL CATALYSTS; ISOCYANIC ACID; NH3; STORAGE; CO; TIO2; SCR; AFTERTREATMENT; GENERATION;
D O I
10.1016/j.apcatb.2014.09.064
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
We report experimental results for the formation of ammonia from nitric oxide and hydrogen, and from nitric oxide, water and carbon monoxide over silica, alumina and titania supported platinum and palladium catalysts. Temperature programmed reaction experiments in gas flow reactor show a considerable formation of ammonia in the temperature range 200-450 degrees C, which is suppressed by the presence of excess oxygen. However, oxygen sweep experiments show that for the titania supported catalysts minor amounts of oxygen promotes the ammonia formation at low temperatures. In situ DRIFT spectroscopy measurements indicate that cyanate species on the support play an important role in the ammonia formation mechanism. This work shows that alumina supported palladium is a promising system for passive selective catalytic reduction applications, exhibiting low-temperature activity during the water gas-shift assisted ammonia formation reaction. Conversely, titania supported samples are less active for ammonia formation as a result of the poor thermal stability of the titania support. (C) 2014 Elsevier B.V. All rights reserved.
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页码:10 / 19
页数:10
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