Dispersion of molybdena on CeO(2), ZrO(2) (Tet), and a mixture of CeO(2) and ZrO(2) (Tet), was investigated by using laser Raman spectroscopy (LRS), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and temperature programmed reduction (TPR). The results indicate that molybdena is dispersed on both individual oxide support and mixed oxide support at the adopted molybdena loadings (0.2 and 0.8 mmol Mo(6+)/100 m(2)) and the structure of the supported molybdena species is intimate association with its loading amount. Two molybdena species are identified by Raman results, i.e. isolated MoO(4)(2-) species at 0.2 mmol Mo(6+)/100 m(2) and polymolybdate species at 0.8 mmol Mo(6+)/100 m(2). IR spectra of ammonia adsorption prove that isolated MoO(4)(2-) species are Lewis acid sites on the Mo/Ce and/or Zr samples, and the polymolybdate species are Brönsted acid sites on the Mo/Ce and/or Zr samples. Moreover, a combination of the Raman, IR and TPR results confirms that at 0.2 mmol Mo(6+)/100 m(2) Ce+Zr, molybdena is preferentially dispersed on the surface of CeO(2) when a mixed oxide support (CeO(2) and ZrO(2)) is present, which was explained in term of the difference of the surface basicity between CeO(2) and ZrO(2) (Tet). Surface structures of the oxide supports were also taken into consideration.
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http://dx.doi.org/10.1016/j.jcis.2008.07.036 | DOI Listing |
J Environ Sci (China)
June 2025
School of Rare Earths, University of Science and Technology of China, Hefei 230026, China; Ganjiang Innovation Academy, Chinese Academy of Sciences, Ganzhou 341000, China; State Key Joint Laboratory of Environment Simulation and Pollution Control, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Two kinds of oxide-zeolite composite support, Ce-beta and Zr-beta were prepared by a simple wet impregnation method and adopted for the preparation of palladium-based catalysts for catalytic oxidation of methane. The Pd/6.8Zr-beta catalyst showed superior methane oxidation performance, achieving T and T of 417 °C and 451 °C, respectively, together with robust hydrothermal stability.
View Article and Find Full Text PDFDalton Trans
November 2024
Advanced Science Research Center, Japan Atomic Energy Agency (JAEA), 2-4 Shirakata, Tokai-mura, Naka-gun, Ibaraki 319-1195, Japan.
The solid-solution aqueous-solution (SSAS) system often involves dissolution/precipitation and redox reactions simultaneously. Comprehensive understanding of the SSAS system requires mechanistic insights into the dissolution mechanism of the solid solution based on reliable characterisation of the solid phases. Given this background, this study investigates the dissolution behaviour of zirconium-cerium oxide solid solution ((Zr,Ce)O/(Ce,Zr)O), which contains the redox-active metal Ce (Ce(III/IV)) and is of particular importance in the nuclear industry.
View Article and Find Full Text PDFBioresour Technol
December 2024
School of Environmental Engineering, University of Seoul, Seoul 02504, Republic of Korea. Electronic address:
The pervasive generation of sewage sludge (SES) and deficiencies in its disposal methods have resulted in several significant environmental and human health challenges. This study explored the catalytic effect of nickel (Ni)-based CeO, ZrO, Zr.Ce.
View Article and Find Full Text PDFChemSusChem
September 2024
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, 980-8577, Japan.
Rise of the mute assassin "carbon monoxide (CO)" levels impact all aerobic life. The elevated rates of CO concentration endure climatic and geographical characteristics that exacerbate air pollution. Herein, a simple approach for hydrothermal leaching (HyTL) of AlTM-Rh (Target material (TM)=Zr, V, Ce) and AlTM (TM=Zr, V, Ce) intermetallic compounds produces leached products of ZrO, VO, and CeO with Rhodium (Rh) as an active component.
View Article and Find Full Text PDFNanoscale
September 2024
Institute of Inorganic Chemistry, Kiel University, Max-Eyth-Str. 2, 24118 Kiel, Germany.
Aiming at a comprehensive understanding of support effects on Ni-based bimetallic catalyst for CO hydrogenation, spectroscopy (DRIFTS) with CO as a probe molecule and temperature-programmed techniques were used to investigate the impact of different supports (MgO, CeO, ZrO) on Ni- and Ni,Fe catalysts. Kinetic parameters revealed that the higher selectivity to methanation for Ni and Ni,Fe supported on the reducible oxides (CeO, ZrO) is due to the inhibition of reverse water-gas shift reaction (RWGS) by hydrogen. A promoting effect of Fe on Ni was only observed on MgO-supported catalysts.
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