Journal article
Highly dispersed CuyAlOx mixed oxides as superior low-temperature alkali metal and SO2 resistant NH3- SCR catalysts
- Abstract:
- For NO x removal from the exhaust gases of municipal solid waste (MSW) incinerators by selective catalytic reduction (SCR) technology, a suitable SCR catalyst which is active at low temperatures and robust to the presence of alkali metals and SO 2 is highly desired. In this contribution, we report the successful fabrication of a highly dispersed Cu y AlO x (y = 2–4) mixed oxides for NH 3 -SCR catalyst using high surface area, flower-like highly dispersed AMO-Cu-Al-CO 3 LDHs precursors. The influence of the Cu/Al ratio (2, 3, 4, and 5), calcination temperature (400, 500, 600, and 700 °C), and testing temperature (150, 200, 250, and 300 °C) on the activity of the Cu y AlO x mixed oxide catalysts were systematically investigated. Among all samples, Cu 4 AlO x showed the highest NO x conversion of 91.1% at 200 °C. After being thermally treated at 700 °C, the NO x conversion of Cu 4 AlO x was still as high as 84.7%, which is much higher than that of the control catalyst 10 wt% CuO/γ-Al 2 O 3 (57.5%). XRD and HR-TEM analyses suggested that the highly dispersed CuO nanoparticles are the active species for the SCR reaction. The catalytic De-NO x performance of Cu 4 AlO x in the presence of alkali metals (K and Na) and SO 2 was also studied. In the presence of 50 ppm SO 2 , the NO x conversion of Cu 4 AlO x (78.4%) was much higher than that of CuO/γ-Al 2 O 3 (48%). The selectivity of NO x conversion to N 2 and resistance to H 2 O (and co-existence of H 2 O and SO 2 ) for Cu 4 AlO x catalyst were also evaluated. In all, we have demonstrated that the newly obtained Cu 4 AlO x catalyst not only possesses higher thermal stability and higher low temperature (150–250 °C) catalytic activity, but also has much better alkali metal (K and Na), SO 2 , and H 2 O resistance than a conventional CuO/γ-Al 2 O 3 catalyst.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Accepted manuscript, pdf, 1.9MB, Terms of use)
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- Publisher copy:
- 10.1016/j.apcata.2017.03.021
Authors
- Publisher:
- Elsevier
- Journal:
- Applied Catalysis A: General More from this journal
- Volume:
- 538
- Pages:
- 37-50
- Publication date:
- 2017-03-18
- Acceptance date:
- 2017-03-17
- DOI:
- ISSN:
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0926-860X
- Keywords:
- Pubs id:
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pubs:689326
- UUID:
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uuid:49dd6e99-5422-4940-ad8f-5779f195ccdc
- Local pid:
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pubs:689326
- Source identifiers:
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689326
- Deposit date:
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2017-08-16
- ARK identifier:
Terms of use
- Copyright holder:
- © 2017 Elsevier BV All rights reserved
- Copyright date:
- 2017
- Notes:
- This is the author accepted manuscript following peer review version of the article. The final version is available online from Elsevier at: 10.1016/j.apcata.2017.03.021
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