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Activity and thermal aging stability of La1−xSrxMnO3 (x = 0.0, 0.3, 0.5, 0.7) and Ir/La1−xSrxMnO3 catalysts for CO oxidation with excess O2

Drosou Aikaterini, Nikolaraki Ersi, Nikolaou Vasileios, Koilia Evangelia, Artemakis Georgios, Stratakis Antonios, Evdou Antigoni, Charisiou Nikolaos D., Goula Maria A., Zaspalis Vasilios, Gentekakis Ioannis

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URIhttp://purl.tuc.gr/dl/dias/BE49C906-49B8-43A6-B0E8-0E6DCF8EC901-
Αναγνωριστικόhttps://doi.org/10.3390/nano13040663-
Αναγνωριστικόhttps://www.mdpi.com/2079-4991/13/4/663-
Γλώσσαen-
Μέγεθος20 pagesen
ΤίτλοςActivity and thermal aging stability of La1−xSrxMnO3 (x = 0.0, 0.3, 0.5, 0.7) and Ir/La1−xSrxMnO3 catalysts for CO oxidation with excess O2en
ΔημιουργόςDrosou Aikaterinien
ΔημιουργόςΔροσου Αικατερινηel
ΔημιουργόςNikolaraki Ersien
ΔημιουργόςΝικολαρακη Ερσηel
ΔημιουργόςNikolaou Vasileiosen
ΔημιουργόςΝικολαου Βασιλειοςel
ΔημιουργόςKoilia Evangeliaen
ΔημιουργόςΚοιλια Ευαγγελιαel
ΔημιουργόςArtemakis Georgiosen
ΔημιουργόςΑρτεμακης Γεωργιοςel
ΔημιουργόςStratakis Antoniosen
ΔημιουργόςΣτρατακης Αντωνιοςel
ΔημιουργόςEvdou Antigonien
ΔημιουργόςCharisiou Nikolaos D.en
ΔημιουργόςGoula Maria A.en
ΔημιουργόςZaspalis Vasiliosen
ΔημιουργόςGentekakis Ioannisen
ΔημιουργόςΓεντεκακης Ιωαννηςel
ΕκδότηςMDPIen
ΠεριγραφήThe authors gratefully acknowledge that this research has been cofinanced by the European Union and Greek national funds under the call “Greece–China Call for Proposals for Joint RT&D Projects”. Project title: Development of new Catalysts for Efficient De-NOX Abatement of Automobile Exhaust Purification (Project code: T7DKI-00356).en
ΠερίληψηThe catalytic oxidation of CO is probably the most investigated reaction in the literature, for decades, because of its extended environmental and fundamental importance. In this paper, the oxidation of CO on La1−xSrxMnO3 perovskites (LSMx), either unloaded or loaded with dispersed Ir nanoparticles (Ir/LSMx), was studied in the temperature range 100–450 °C under excess O2 conditions (1% CO + 5% O2). The perovskites, of the type La1−xSrxMnO3 (x = 0.0, 0.3, 0.5 and 0.7), were prepared by the coprecipitation method. The physicochemical and structural properties of both the LSMx and the homologous Ir/LSMx catalysts were evaluated by various techniques (XRD, N2 sorption–desorption by BET-BJH, H2-TPR and H2-Chem), in order to better understand the structure–activity–stability correlations. The effect of preoxidation/prereduction/aging of the catalysts on their activity and stability was also investigated. Results revealed that both LSMx and Ir/LSMx are effective for CO oxidation, with the latter being superior to the former. In both series of materials, increasing the substitution of La by Sr in the composition of the perovskite resulted to a gradual suppression of their CO oxidation activity when these were prereduced; the opposite was true for preoxidized samples. Inverse hysteresis phenomena in activity were observed during heating/cooling cycles on the prereduced Ir/LSMx catalysts with the loop amplitude narrowing with increasing Sr-content in LSMx. Oxidative thermal sintering experiments at high temperatures revealed excellent antisintering behavior of Ir nanoparticles supported on LSMx, resulting from perovskite’s favorable antisintering properties of high oxygen storage capacity and surface oxygen vacancies.en
ΤύποςPeer-Reviewed Journal Publicationen
ΤύποςΔημοσίευση σε Περιοδικό με Κριτέςel
Άδεια Χρήσηςhttp://creativecommons.org/licenses/by/4.0/en
Ημερομηνία2025-06-05-
Ημερομηνία Δημοσίευσης2023-
Θεματική ΚατηγορίαCO oxidationen
Θεματική ΚατηγορίαExcess O2 conditionsen
Θεματική ΚατηγορίαLSM perovskitesen
Θεματική ΚατηγορίαIridium nanoparticlesen
Θεματική ΚατηγορίαHysteresis phenomenaen
Θεματική ΚατηγορίαIsothermal steady-state multiplicityen
Βιβλιογραφική ΑναφοράC. Drosou, E. Nikolaraki, V. Nikolaou, E. Koilia, G. Artemakis, A. Stratakis, A. Evdou, N. D. Charisiou, M. A. Goula, V. Zaspalis and I. V. Yentekakis, “Activity and thermal aging stability of La1−xSrxMnO3 (x = 0.0, 0.3, 0.5, 0.7) and Ir/La1−xSrxMnO3 catalysts for CO oxidation with excess O2,” Nanomaterials, vol. 13, no. 4, Feb. 2023, doi: 10.3390/nano13040663.en

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