A highly active and stable Pt modified molybdenum carbide catalyst for steam reforming of dimethyl ether and the reaction pathway |
| |
| Affiliation: | 1. Hydrogen Production and Utilization Laboratory, Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou, 510640, China;2. Guangdong Key Laboratory of New and Renewable Energy Research and Development, Guangzhou, 510640, China;3. University of Chinese Academy of Sciences, Beijing, 100049, China;4. Dongguan Baida New Energy Shares Co., Ltd, Dongguan, 523808, China;1. D. Mendeleev University of Chemical Technology of Russia, Moscow, Russia;2. NRC Kurchatov Institute, Moscow, Russia;3. Politecnico di Torino, Torino, Italy;1. Institute of Energy Technologies, Universitat Politècnica de Catalunya, EEBE, Eduard Maristany 16, 08019 Barcelona, Spain;2. Planta Piloto de Ingeniería Química, UNS, CONICET, Camino La Carrindanga km 7, 8000 Bahía Blanca, Argentina;3. Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya, EEBE, Eduard Maristany 16, 08019 Barcelona, Spain;4. Department of Electronic Engineering, Universitat Politècnica de Catalunya, Campus Nord, Jordi Girona 1-3, 08034 Barcelona, Spain;5. Department of Chemical Engineering, Universitat Politècnica de Catalunya, EEBE, Eduard Maristany 16, 08019 Barcelona, Spain;1. Depart. of Mechanical Eng., Chonnam National University, 77 Yongbong-ro, Bug-gu, Gwangju, 61186, Republic of Korea;2. School of Mechanical Eng., Automobile Research Center, 77 Yongbong-ro, Bug-gu, Chonnam National University, Gwangju, 61186, Republic of Korea |
| |
| Abstract: | To improve the stability of molybdenum carbide catalysts in dimethyl ether steam reforming (DSR), the inactivation mechanism and the performance of Pt modified catalyst has been investigated. The Mo2C oxidation induced by H2O is verified to be the main reason of catalytic deactivation. After modified with Pt, the H2 production rate and selectivity are greatly enhanced, reaches 1605 μmol min−1·gcat−1 at 350 °C, in comparison to that of the Mo2C/Al2O3 catalyst. Moreover, the 2%Pt–Mo2C/Al2O3 catalyst is more stable with only 20% activity loss after 50 h on stream compares to the 73% activity loss in 12 h with Mo2C/Al2O3 catalyst. By means of in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), the enhancement brought by Pt is ascribed to the consumption acceleration of intermediate oxygen species on catalyst surface and the decline of onset temperature of DSR reaction. It is expected that these findings can lead us to more practical molybdenum carbide catalysts in DSR. |
| |
| Keywords: | Steam reforming Dimethyl ether Molybdenum carbide Oxidation mechanism |
| 本文献已被 ScienceDirect 等数据库收录！ |
|
