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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...

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Detalles Bibliográficos
Autores principales: Qian, Xiaoshuang, Qin, Hongmei, Meng, Tao, Lin, Yi, Ma, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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
Descripción
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.