Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study

© 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. The reaction mechanism of the selective catalytic reduction of NO by NH3 (NH3-SCR) on an oxotitanium-porphyrin catalyst was systematically investigated by using density functional theory calculations with the...

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Main Authors: Rathawat Daengngern, Phornphimon Maitarad, Liyi Shi, Dengsong Zhang, Nawee Kungwan, Vinich Promarak, Jittima Meeprasert, Supawadee Namuangruk
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Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/62620
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spelling th-cmuir.6653943832-626202018-11-29T07:47:49Z Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study Rathawat Daengngern Phornphimon Maitarad Liyi Shi Dengsong Zhang Nawee Kungwan Vinich Promarak Jittima Meeprasert Supawadee Namuangruk Chemical Engineering Chemistry Materials Science © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. The reaction mechanism of the selective catalytic reduction of NO by NH3 (NH3-SCR) on an oxotitanium-porphyrin catalyst was systematically investigated by using density functional theory calculations with the M06L functional. The reaction was proposed to follow the nitrite mechanism over the two forms of active sites; the oxotitanium-porphyrin Lewis acid site (TiO-por) and the Brønsted acid site (TiOH-por). The reaction path consisted of (i) nitrite formation, (ii) NH3 oxidation, (iii) formation of NH2NO and NHNOH intermediates, and (iv) N2 and H2O product formation. The obtained calculations showed that the formation of the NHNOH intermediate was the rate determining step for both active sites with the energy barriers (Ea) of 32.2 and 36.2 kcal mol-1 for the Lewis and Brønsted acid sites, respectively. It is worth noting that the activation energy for NHNOH formation over the oxotitanium-porphyrin active sites was found to be in the same range as that of vanadium oxide cluster models. Furthermore, the product formations of N2 and H2O over the Lewis and Brønsted acid sites of oxotitanium-porphyrin were exothermic processes with reaction energies (Er) of -67.1 and -39.0 kcal mol-1, respectively. Thus, in conclusion, the oxotitanium-porphyrin could theoretically act as an alternative catalyst for NH3-SCR of NO and it would be challenging to test it in experimental studies. 2018-11-29T07:36:03Z 2018-11-29T07:36:03Z 2018-01-01 Journal 13699261 11440546 2-s2.0-85054978281 10.1039/c8nj03616k https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054978281&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62620
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Chemical Engineering
Chemistry
Materials Science
spellingShingle Chemical Engineering
Chemistry
Materials Science
Rathawat Daengngern
Phornphimon Maitarad
Liyi Shi
Dengsong Zhang
Nawee Kungwan
Vinich Promarak
Jittima Meeprasert
Supawadee Namuangruk
Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study
description © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. The reaction mechanism of the selective catalytic reduction of NO by NH3 (NH3-SCR) on an oxotitanium-porphyrin catalyst was systematically investigated by using density functional theory calculations with the M06L functional. The reaction was proposed to follow the nitrite mechanism over the two forms of active sites; the oxotitanium-porphyrin Lewis acid site (TiO-por) and the Brønsted acid site (TiOH-por). The reaction path consisted of (i) nitrite formation, (ii) NH3 oxidation, (iii) formation of NH2NO and NHNOH intermediates, and (iv) N2 and H2O product formation. The obtained calculations showed that the formation of the NHNOH intermediate was the rate determining step for both active sites with the energy barriers (Ea) of 32.2 and 36.2 kcal mol-1 for the Lewis and Brønsted acid sites, respectively. It is worth noting that the activation energy for NHNOH formation over the oxotitanium-porphyrin active sites was found to be in the same range as that of vanadium oxide cluster models. Furthermore, the product formations of N2 and H2O over the Lewis and Brønsted acid sites of oxotitanium-porphyrin were exothermic processes with reaction energies (Er) of -67.1 and -39.0 kcal mol-1, respectively. Thus, in conclusion, the oxotitanium-porphyrin could theoretically act as an alternative catalyst for NH3-SCR of NO and it would be challenging to test it in experimental studies.
format Journal
author Rathawat Daengngern
Phornphimon Maitarad
Liyi Shi
Dengsong Zhang
Nawee Kungwan
Vinich Promarak
Jittima Meeprasert
Supawadee Namuangruk
author_facet Rathawat Daengngern
Phornphimon Maitarad
Liyi Shi
Dengsong Zhang
Nawee Kungwan
Vinich Promarak
Jittima Meeprasert
Supawadee Namuangruk
author_sort Rathawat Daengngern
title Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study
title_short Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study
title_full Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study
title_fullStr Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study
title_full_unstemmed Oxotitanium-porphyrin for selective catalytic reduction of NO by NH<inf>3</inf>: A theoretical mechanism study
title_sort oxotitanium-porphyrin for selective catalytic reduction of no by nh<inf>3</inf>: a theoretical mechanism study
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054978281&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62620
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