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Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water

The catalytic reduction of nitrites over Pt-In catalysts supported on activated carbon has been studied in a semi-batch reactor, at room temperature and atmospheric pressure, and using hydrogen as the reducing agent. The influence of the indium content on the activity and selectivity was evaluated....

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Autores principales: Soares, Olívia Salomé G. P., Jardim, Erika O., Ramos-Fernandez, Enrique V., Villora-Picó, Juan J., Pastor-Blas, M. Mercedes, Silvestre-Albero, Joaquín, Órfão, José J. M., Pereira, Manuel Fernando R., Sepúlveda-Escribano, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374164/
https://www.ncbi.nlm.nih.gov/pubmed/34422775
http://dx.doi.org/10.3389/fchem.2021.733881
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author Soares, Olívia Salomé G. P.
Jardim, Erika O.
Ramos-Fernandez, Enrique V.
Villora-Picó, Juan J.
Pastor-Blas, M. Mercedes
Silvestre-Albero, Joaquín
Órfão, José J. M.
Pereira, Manuel Fernando R.
Sepúlveda-Escribano, Antonio
author_facet Soares, Olívia Salomé G. P.
Jardim, Erika O.
Ramos-Fernandez, Enrique V.
Villora-Picó, Juan J.
Pastor-Blas, M. Mercedes
Silvestre-Albero, Joaquín
Órfão, José J. M.
Pereira, Manuel Fernando R.
Sepúlveda-Escribano, Antonio
author_sort Soares, Olívia Salomé G. P.
collection PubMed
description The catalytic reduction of nitrites over Pt-In catalysts supported on activated carbon has been studied in a semi-batch reactor, at room temperature and atmospheric pressure, and using hydrogen as the reducing agent. The influence of the indium content on the activity and selectivity was evaluated. Monometallic Pt catalysts are very active for nitrite reduction, but the addition of up to 1 wt% of indium significantly increases the nitrogen selectivity from 0 to 96%. The decrease in the accessible noble metal surface area reduces the amount of hydrogen available at the catalyst surface, this favoring the combination of nitrogen-containing intermediate molecules to promote the formation of N(2) instead of being deeply hydrogenated into NH(4+). Several activated carbon-supported Pt-In catalysts, activated under different calcination and reduction temperatures, have been also evaluated in nitrite reduction. The catalyst calcined and reduced at 400°C showed the best performance considering both the activity and the selectivity to nitrogen. This enhanced selectivity is ascribed to the formation of Pt-In alloy. The electronic properties of Pt change upon alloy formation, as it is demonstrated by XPS.
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spelling pubmed-83741642021-08-20 Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water Soares, Olívia Salomé G. P. Jardim, Erika O. Ramos-Fernandez, Enrique V. Villora-Picó, Juan J. Pastor-Blas, M. Mercedes Silvestre-Albero, Joaquín Órfão, José J. M. Pereira, Manuel Fernando R. Sepúlveda-Escribano, Antonio Front Chem Chemistry The catalytic reduction of nitrites over Pt-In catalysts supported on activated carbon has been studied in a semi-batch reactor, at room temperature and atmospheric pressure, and using hydrogen as the reducing agent. The influence of the indium content on the activity and selectivity was evaluated. Monometallic Pt catalysts are very active for nitrite reduction, but the addition of up to 1 wt% of indium significantly increases the nitrogen selectivity from 0 to 96%. The decrease in the accessible noble metal surface area reduces the amount of hydrogen available at the catalyst surface, this favoring the combination of nitrogen-containing intermediate molecules to promote the formation of N(2) instead of being deeply hydrogenated into NH(4+). Several activated carbon-supported Pt-In catalysts, activated under different calcination and reduction temperatures, have been also evaluated in nitrite reduction. The catalyst calcined and reduced at 400°C showed the best performance considering both the activity and the selectivity to nitrogen. This enhanced selectivity is ascribed to the formation of Pt-In alloy. The electronic properties of Pt change upon alloy formation, as it is demonstrated by XPS. Frontiers Media S.A. 2021-08-05 /pmc/articles/PMC8374164/ /pubmed/34422775 http://dx.doi.org/10.3389/fchem.2021.733881 Text en Copyright © 2021 Soares, Jardim, Ramos-Fernandez, Villora-Picó, Pastor-Blas, Silvestre-Albero, Órfão, Pereira and Sepúlveda-Escribano. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Soares, Olívia Salomé G. P.
Jardim, Erika O.
Ramos-Fernandez, Enrique V.
Villora-Picó, Juan J.
Pastor-Blas, M. Mercedes
Silvestre-Albero, Joaquín
Órfão, José J. M.
Pereira, Manuel Fernando R.
Sepúlveda-Escribano, Antonio
Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water
title Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water
title_full Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water
title_fullStr Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water
title_full_unstemmed Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water
title_short Highly N(2)-Selective Activated Carbon-Supported Pt-In Catalysts for the Reduction of Nitrites in Water
title_sort highly n(2)-selective activated carbon-supported pt-in catalysts for the reduction of nitrites in water
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374164/
https://www.ncbi.nlm.nih.gov/pubmed/34422775
http://dx.doi.org/10.3389/fchem.2021.733881
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