Hydrothermal synthesis of manganese oxide nanorods as a highly active support for gold nanoparticles in CO oxidation and their stability at low temperature
Nanostructured mesoporous α-MnO 2 nanorods were synthesized via a simple hydrothermal process using MnSO 4 ·H 2 O and KMnO 4 as precursors. A series of Au/MnO 2 catalysts were prepared by a colloidal deposition (CD) method and were characterized by X-ray diffraction (XRD), nitrogen adsorption, scann...
Gespeichert in:
Veröffentlicht in: | RSC advances 2015-01, Vol.5 (77), p.62732-62738 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Nanostructured mesoporous α-MnO
2
nanorods were synthesized
via
a simple hydrothermal process using MnSO
4
·H
2
O and KMnO
4
as precursors. A series of Au/MnO
2
catalysts were prepared by a colloidal deposition (CD) method and were characterized by X-ray diffraction (XRD), nitrogen adsorption, scanning electron microscopy (SEM) and temperature programmed reduction of hydrogen (H
2
-TPR) analysis. The influence of the preparation conditions of the supports on the catalytic performance of Au/MnO
2
catalysts in CO oxidation has been investigated. The results show that the structure and properties of MnO
2
products were strongly dependent on the hydrothermal time. One can distinguish the aspect ratio of MnO
2
nanorods from SEM images. The obtained Au/MnO
2
catalysts with 1 wt% Au exhibits excellent performance with a complete CO conversion at 20 °C (
T
100%
= 20 °C) and 50% CO conversion at −25 °C (
T
50%
= −25 °C). Furthermore, H
2
-TPR studies reveal the superior activities have been attributed to the support unique reducibility and the interaction between Au and support. However, the U-shaped activity curves show a significant drop in CO conversion at low-temperature. With the help of temperature programmed desorption (CO
2
-TPD) and CO
2
static adsorption studies, it confirms that the deactivation of catalytic activity was attributed to the adsorbed CO
2
taking up the active sites, which can be desorbed by increasing the reaction temperature.
One active Au/MnO
2
catalysts were prepared by a colloidal deposition method. The deactivation was studied by temperature programmed desorption of CO
2
analysis. |
---|---|
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c5ra12182e |