Direct NO decomposition over Rh-supported catalysts for exhaust emission control

被引:1
|
作者
Bin Bae, Wo [1 ,2 ]
Kim, Do Yeong [1 ,2 ]
Byun, Sang Woo [1 ,2 ]
Lee, Seong Jun [3 ]
Kuk, Su Keun [4 ]
Kwon, Hyuk Jae [4 ]
Lee, Hyun Chul [4 ]
Hazlett, Melanie J. [5 ]
Liu, Chong [6 ]
Kim, Young Jin [7 ]
Kim, Minkyu [3 ]
Kang, Sung Bong [1 ,2 ]
机构
[1] Gwangju Inst Sci & Technol, Res Ctr Innovat Energy & Carbon Optimized Synth Ch, 123 Cheomdan Gwagiro, Gwangju 61005, South Korea
[2] Gwangju Inst Sci & Technol, Sch Earth Sci & Environm Engn, 123 Cheomdan Gwagiro, Gwangju 61005, South Korea
[3] Yeungnam Univ, Sch Chem Engn, 280 Daehak Ro, Gyongsan 38541, South Korea
[4] Samsung Elect Co Ltd, Samsung Adv Inst Technol, 130 Smaung Ro, Suwon 16678, Gyeonggi, South Korea
[5] Concordia Univ, Gina Cody Sch Engn & Comp Sci, Chem & Mat Engn, Montreal, PQ H4B 1R6, Canada
[6] Univ Calif Los Angeles, Dept Chem & Biochem, 607 Charles E Young Dr East, Los Angeles, CA 90024 USA
[7] Korea Res Inst Chem Technol, Ctr Environm & Sustainable Resources Res, 141 Gajeong Ro, Daejeon 34114, South Korea
基金
新加坡国家研究基金会;
关键词
Direct NO decomposition; Rh/PrO X; Deactivation; Rh active sites; Regeneration; NITRIC-OXIDE; SURFACE; N-2; O-2; MECHANISM; STATES; AL2O3; LAYER; CEO2; H-2;
D O I
10.1016/j.cej.2023.146005
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Direct nitrogen oxide decomposition (DND) is a promising alternative to the selective catalytic reduction (SCR) of nitrogen oxides for emissions control, as it eliminates the need to inject reductants such as urea/ammonia. The present study investigates the implementation of Rh-supported metal oxides for the DND reaction. Rh supported on each of PrOX, TiO2, Al2O3, and CeO2 were characterized, and we found that initially the catalytic activity on Rh/PrOX and Rh/TiO2 was very high, though it deactivated over time due to strong poisoning by adsorbed oxygen. This deactivation by oxygen poisoning was verified through in-situ DRIFTS, XPS, NEXAFS, O2-TPD measurements and density functional theory (DFT) calculations, respectively. This catalytic deactivation was positively regenerated by reductive treatments with CO or H2. This study discovers the mechanism of DND deactivation and regeneration over Rh-supported metal oxides, which will provide significant insight into further development of DND.
引用
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页数:12
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