NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism

The NOx storage mechanism on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> catalyst were studied using different techniques. The results obtained by XRD, ATR, TGA and XPS under NOx storage–regeneration conditions revealed that BaO generated on the catalyst by de...

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Main Authors: Vicente Albaladejo-Fuentes, María-Salvadora Sánchez-Adsuar, James A. Anderson, María-José Illán-Gómez
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/11/8/2133
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author Vicente Albaladejo-Fuentes
María-Salvadora Sánchez-Adsuar
James A. Anderson
María-José Illán-Gómez
author_facet Vicente Albaladejo-Fuentes
María-Salvadora Sánchez-Adsuar
James A. Anderson
María-José Illán-Gómez
author_sort Vicente Albaladejo-Fuentes
collection DOAJ
description The NOx storage mechanism on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> catalyst were studied using different techniques. The results obtained by XRD, ATR, TGA and XPS under NOx storage–regeneration conditions revealed that BaO generated on the catalyst by decomposition of Ba<sub>2</sub>TiO<sub>4</sub> plays a key role in the NOx storage process. In situ DRIFTS experiments under NO/O<sub>2</sub> and NO/N<sub>2</sub> show that nitrites and nitrates are formed on the perovskite during the NOx storage process. Thus, it seems that, as for model NSR catalysts, the NOx storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> catalyst takes place by both “nitrite” and “nitrate” routes, with the main pathway being highly dependent on the temperature and the time on stream: (i) at T < 350 °C, NO adsorption leads to nitrites formation on the catalyst and (ii) at T > 350 °C, the catalyst activity for NO oxidation promotes NO<sub>2</sub> generation and the nitrate formation.
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spelling doaj.art-c8f32d93060143a2a8c2c54d7a67deea2023-11-22T09:01:00ZengMDPI AGNanomaterials2079-49912021-08-01118213310.3390/nano11082133NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible MechanismVicente Albaladejo-Fuentes0María-Salvadora Sánchez-Adsuar1James A. Anderson2María-José Illán-Gómez3Carbon Materials and Environment Research Group, Department of Inorganic Chemistry, Faculty of Science, Universidad de Alicante San Vicente del Raspeig, 03690 Alicante, SpainCarbon Materials and Environment Research Group, Department of Inorganic Chemistry, Faculty of Science, Universidad de Alicante San Vicente del Raspeig, 03690 Alicante, SpainSurface Chemistry and Catalysis Group, School of Engineering, University of Aberdeen, Aberdeen AB24 3UE, UKCarbon Materials and Environment Research Group, Department of Inorganic Chemistry, Faculty of Science, Universidad de Alicante San Vicente del Raspeig, 03690 Alicante, SpainThe NOx storage mechanism on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> catalyst were studied using different techniques. The results obtained by XRD, ATR, TGA and XPS under NOx storage–regeneration conditions revealed that BaO generated on the catalyst by decomposition of Ba<sub>2</sub>TiO<sub>4</sub> plays a key role in the NOx storage process. In situ DRIFTS experiments under NO/O<sub>2</sub> and NO/N<sub>2</sub> show that nitrites and nitrates are formed on the perovskite during the NOx storage process. Thus, it seems that, as for model NSR catalysts, the NOx storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> catalyst takes place by both “nitrite” and “nitrate” routes, with the main pathway being highly dependent on the temperature and the time on stream: (i) at T < 350 °C, NO adsorption leads to nitrites formation on the catalyst and (ii) at T > 350 °C, the catalyst activity for NO oxidation promotes NO<sub>2</sub> generation and the nitrate formation.https://www.mdpi.com/2079-4991/11/8/2133NOx storage mechanismin situ DRIFTSnitritesnitratesbarium-titanium perovskite
spellingShingle Vicente Albaladejo-Fuentes
María-Salvadora Sánchez-Adsuar
James A. Anderson
María-José Illán-Gómez
NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism
Nanomaterials
NOx storage mechanism
in situ DRIFTS
nitrites
nitrates
barium-titanium perovskite
title NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism
title_full NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism
title_fullStr NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism
title_full_unstemmed NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism
title_short NOx Storage on BaTi<sub>0.8</sub>Cu<sub>0.2</sub>O<sub>3</sub> Perovskite Catalysts: Addressing a Feasible Mechanism
title_sort nox storage on bati sub 0 8 sub cu sub 0 2 sub o sub 3 sub perovskite catalysts addressing a feasible mechanism
topic NOx storage mechanism
in situ DRIFTS
nitrites
nitrates
barium-titanium perovskite
url https://www.mdpi.com/2079-4991/11/8/2133
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AT jamesaanderson noxstorageonbatisub08subcusub02subosub3subperovskitecatalystsaddressingafeasiblemechanism
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