Support effect of Ni/mesoporous silica catalysts for CO2 reforming of CH4

被引:9
作者
Chen, Jing [1 ,2 ]
Piao, Wen Xiang [1 ,2 ]
Jin, Long Yi [1 ,2 ]
Li, Zhenghua [3 ]
Zhang, Fan [1 ,2 ]
Kim, Ji Man [3 ]
Jin, Mingshi [1 ,2 ]
机构
[1] Yanbian Univ, Key Lab Nat Resource Changbai Mt & Funct Mol, Minist Educ, Pk Rd 977, Yanji 133002, Peoples R China
[2] Yanbian Univ, Dept Chem, Coll Sci, Pk Rd 977, Yanji 133002, Peoples R China
[3] Sungkyunkwan Univ, Dept Chem, Suwon 440746, South Korea
基金
新加坡国家研究基金会; 中国国家自然科学基金;
关键词
Ni catalyst; Impregnation; Mesoporous silica; Methane reforming; Carbon dioxide; CARBON-DIOXIDE; SYNTHESIS GAS; NICKEL-CATALYSTS; NI CATALYSTS; PARTIAL OXIDATION; MESOPOROUS SILICAS; SOLID-SOLUTION; NOBLE-METALS; METHANE; PERFORMANCE;
D O I
10.1007/s11164-018-3389-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mesoporous silica KIT-6-, SBA-15-, and MCM-41-supported Ni catalysts (Ni/KIT-6, Ni/SBA-15, and Ni/MCM-41) were prepared via impregnation method and studied for CO2 reforming of CH4. The catalysts were characterized by X-ray diffraction analysis, N-2 physisorption measurements, scanning electron microscopy, transmission electron microscopy, and temperature-programmed oxidation (O-2-TPO). The Ni/KIT-6 catalyst exhibited higher catalytic activity and long-term stability compared with Ni/SBA-15 or Ni/MCM-41. The conversion of CH4 and CO2 over Ni/KIT-6 was 99 and 99 %, respectively. The superior catalytic behavior of Ni/KIT-6 is closely related to the large-pore cubic Ia3d structure of KIT-6, which enhanced dispersion of Ni nanoparticles, reduced carbon deposition, and increased diffusion of reactant and products. [GRAPHICS] .
引用
收藏
页码:3867 / 3878
页数:12
相关论文
共 38 条
[1]   PARTIAL OXIDATION OF METHANE TO SYNTHESIS GAS-USING CARBON-DIOXIDE [J].
ASHCROFT, AT ;
CHEETHAM, AK ;
GREEN, MLH ;
VERNON, PDF .
NATURE, 1991, 352 (6332) :225-226
[2]  
Bitter J. H., 1996, J CATAL, V55, P161
[3]   Ceria-gadolinia supported NiCu catalyst: A suitable system for dry reforming of biogas to feed a solid oxide fuel cell (SOFC) [J].
Bonura, G. ;
Cannilla, C. ;
Frusteri, F. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2012, 121 :135-147
[4]   CO2 reforming of CH4 [J].
Bradford, MCJ ;
Vannice, MA .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (01) :1-42
[5]   Synthesis gas production from dry reforming of methane over Ce0.75Zr0.25O2-supported Ru catalysts [J].
Chen, Jixiang ;
Yao, Chengcheng ;
Zhao, Yanqiao ;
Jia, Peihong .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2010, 35 (04) :1630-1642
[6]   Promoting effect of Pt, Pd and Rh noble metals to the Ni0.03Mg0.97O solid solution catalysts for the reforming of CH4 with CO2 [J].
Chen, YG ;
Tomishige, K ;
Yokoyama, K ;
Fujimoto, K .
APPLIED CATALYSIS A-GENERAL, 1997, 165 (1-2) :335-347
[7]   Characterization and activity in dry reforming of methane on NiMg/Al and Ni/MgO catalysts [J].
Djaidja, A ;
Libs, S ;
Kiennemann, A ;
Barama, A .
CATALYSIS TODAY, 2006, 113 (3-4) :194-200
[8]   THE ROLE OF CATALYST SUPPORT ON THE ACTIVITY OF NICKEL FOR REFORMING METHANE WITH CO2 [J].
GADALLA, AM ;
BOWER, B .
CHEMICAL ENGINEERING SCIENCE, 1988, 43 (11) :3049-3062
[9]   Production of synthesis gas via methane reforming with CO2 on noble metals and small amount of noble-(Rh-) promoted Ni catalysts [J].
Hou, ZY ;
Chen, P ;
Fang, HL ;
Zheng, XM ;
Yashima, T .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2006, 31 (05) :555-561
[10]   Preparation of Ni/MgO catalyst for CO2 reforming of methane by dielectric-barrier discharge plasma [J].
Hua, Wei ;
Jin, Lijun ;
He, Xinfu ;
Liu, Jiahe ;
Hu, Haoquan .
CATALYSIS COMMUNICATIONS, 2010, 11 (11) :968-972