期刊
MICROPOROUS AND MESOPOROUS MATERIALS
卷 221, 期 -, 页码 204-211出版社
ELSEVIER
DOI: 10.1016/j.micromeso.2015.09.036
关键词
Water gas shift reaction (WGSR); Mesoporous CO3O4; Mn promoter; Structural stability
类别
资金
- Korea Institute of Materials Science [PNK4310]
- National Research Foundation of Korea (NRF) - Korea government [NRF-2014R1A1A2A16055557]
- Industrial Source Technology Development Programs of the Ministry of Knowledge Economy (MKE) of Korea [2013-10042712]
- National Research Council of Science and Technology (NST) through Degree and Research Center (DRC) Program
- National Research Council of Science & Technology (NST), Republic of Korea [PNK4310] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
The novel Mn-modified ordered mesoporous Co3O4 catalysts were investigated for water gas shift reaction (WGSR), which was synthesized through a nano-casting method using a hard template of KIT-6. An incipient wetness impregnation of Mn precursor with different concentrations was applied for preparing Mn-modified mesoporous Co3O4. On 15 wt%Mn impregnated mesoporous Co3O4 (denoted as Mn(15)/meso-Co3O4), WGSR activity was found to be higher among the tested catalysts due to a higher structural stability of the Co3O4 mesopores with a larger surface area. The Mn(15)/meso-Co3O4 also showed stable ordered mesopore structures with an exposed larger number of active metallic cobalt sites on the surfaces even after WGSR. The structural stability was mainly attributed to the strong and stable interactions between cobalt oxides and manganese oxides. With an optimum amount of Mn promoter, Mn plays an important role as a structural stabilizer of the mesoporous Co3O4 as well as an electron modifier by enhancing redox cycle properties of cobalt species and fast mass transport in mesopores. (C) 2015 Elsevier Inc. All rights reserved.
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