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Metal Phosphate-Supported Pt Catalysts for CO Oxidation
Oxides (such as SiO(2), TiO(2), ZrO(2), Al(2)O(3), Fe(2)O(3), CeO(2)) have often been used to prepare supported Pt catalysts for CO oxidation and other reactions, whereas metal phosphate-supported Pt catalysts for CO oxidation were rarely reported. Metal phosphates are a family of metal salts with h...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456429/ https://www.ncbi.nlm.nih.gov/pubmed/28788293 http://dx.doi.org/10.3390/ma7128105 |
Sumario: | Oxides (such as SiO(2), TiO(2), ZrO(2), Al(2)O(3), Fe(2)O(3), CeO(2)) have often been used to prepare supported Pt catalysts for CO oxidation and other reactions, whereas metal phosphate-supported Pt catalysts for CO oxidation were rarely reported. Metal phosphates are a family of metal salts with high thermal stability and acid-base properties. Hydroxyapatite (Ca(10)(PO(4))(6)(OH)(2), denoted as Ca-P-O here) also has rich hydroxyls. Here we report a series of metal phosphate-supported Pt (Pt/M-P-O, M = Mg, Al, Ca, Fe, Co, Zn, La) catalysts for CO oxidation. Pt/Ca-P-O shows the highest activity. Relevant characterization was conducted using N(2) adsorption-desorption, inductively coupled plasma (ICP) atomic emission spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), CO(2) temperature-programmed desorption (CO(2)-TPD), X-ray photoelectron spectroscopy (XPS), and H(2) temperature-programmed reduction (H(2)-TPR). This work furnishes a new catalyst system for CO oxidation and other possible reactions. |
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