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Control of the NO–NH3 SCR Behavior of Cu-ZSM-5 by Variation of the Electronic State of Copper Full article

Conference Eleventh International Congress on Catalysis and Automotive Pollution Control
29-31 Oct 2018 , Brussels
Journal Topics in Catalysis
ISSN: 1022-5528 , E-ISSN: 1572-9028
Output data Year: 2019, Volume: 62, Number: 1-4, Pages: 179-191 SI Pages count : 13 DOI: 10.1007/s11244-018-1101-4
Tags Cu-ZSM-5; Selective catalytic reduction of NOx; NO–NH3 SCR; Ammonia; TPD
Authors Yashnik S.A. 1 , Ismagilov Z.R. 1
Affiliations
1 Boreskov Institute of Catalysis, Novosibirsk 630090, Russia

Funding (1)

1 Federal Agency for Scientific Organizations 0303-2016-0014

Abstract: The effect of NH4OH/Cu2+ in a copper-acetate solution on the properties of ion-exchanged Cu-ZSM-5 catalysts in the selective catalytic reduction of NO by NH3 (NO–NH3 SCR) has been studied. The temperature programmed desorption of ammonia (NH3-TPR) on Cu-ZSM-5 and the ammonia adsorption–desorption dynamics at 75–300 °C were studied to identify and quantify the nature of acid sites and ammonia desorption heat of Cu-ZSM-5. The Cu-ZSM-5 catalysts containing Cu-structures with extra-lattice oxygen were active in the low-temperature SCR, whereas those with isolated Cu2+ ions were active in the high-temperature SCR. It was shown that Cu-structures with extra-lattice oxygen were generated during the ion exchange of H-ZSM-5 with a water-ammonia solution of copper-acetate where the NH4OH/Cu2+ ratio was in the range of 6–15. Isolated Cu2+ ions were produced in the ion-exchange mode with the ammonia-free solution.
Cite: Yashnik S.A. , Ismagilov Z.R.
Control of the NO–NH3 SCR Behavior of Cu-ZSM-5 by Variation of the Electronic State of Copper
Topics in Catalysis. 2019. V.62. N1-4. P.179-191 SI. DOI: 10.1007/s11244-018-1101-4 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Published online: Dec 13, 2018
Published print: Feb 1, 2019
Identifiers:
Web of science: WOS:000461821000023
Scopus: 2-s2.0-85058493328
Elibrary: 38589538
Chemical Abstracts: 2018:2568299
Chemical Abstracts (print): 170:495985
OpenAlex: W2903662334
Citing:
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Scopus 10
Web of science 10
Elibrary 11
OpenAlex 10
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