CO2 conversion to synthesis gas via DRM on the durable Al2O3/Ni/Al2O3 sandwich catalyst with high activity and stability

被引:46
作者
Zhao, Yu [1 ,2 ]
Kang, Yunqing [1 ,2 ]
Li, Hui [1 ,2 ]
Li, Hexing [1 ,2 ,3 ]
机构
[1] Shanghai Normal Univ, Chinese Educ Minist Key Lab, Shanghai 200234, Peoples R China
[2] Shanghai Normal Univ, Int Joint Lab Res Chem, Shanghai 200234, Peoples R China
[3] Shanghai Univ Elect Power, Shanghai 200062, Peoples R China
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
MESOPOROUS CATALYSTS; METHANE; CH4; DEACTIVATION; CA; OXIDE;
D O I
10.1039/c8gc00743h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO2 conversion to synthesis gas with a CO/H-2 molar ratio around 1 was realized by using the dry reforming of methane reaction (DRM) at 800 degrees C. The key problem was to design catalysts with both high activity and strong durability at such a high reaction temperature. This work developed a novel Al2O3/Ni/Al2O3 sandwiched catalyst prepared by coating Al2O3-supported Ni nanoparticles with a porous Al2O3 thin film by atomic layer deposition (ALD). The catalyst with 80 layers of Al2O3 thin films exhibited the highest activity. Both CO2 and CH4 conversions reached nearly 100% with absolute selectivities towards CO and H-2. More importantly, this catalyst displayed excellent stability and could be used for more than 400 h in the DRM reaction at 800 degrees C without significant deactivation. Mechanism analysis revealed that the deactivation mainly resulted from the gathering of Ni nanoparticles at high temperature, corresponding to the decrease of Ni active sites. Moreover, a large-sized Ni active site could easily cause carbon deposition, which could further accelerate the catalyst deactivation. The Al2O3/Ni/Al2O3 sandwiched catalyst could effectively protect Ni nanoparticles from gathering owing to the double strong interactions between the Ni active sites and Al2O3 support.
引用
收藏
页码:2781 / 2787
页数:7
相关论文
共 26 条
  • [1] Supported bimetallic cluster catalysts
    Alexeev, OS
    Gates, BC
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (08) : 1571 - 1587
  • [2] THE INTERLAYER SPACING OF GRAPHITE
    BACON, GE
    [J]. ACTA CRYSTALLOGRAPHICA, 1951, 4 (06): : 558 - 561
  • [3] CO2 reforming of CH4 over supported Pt catalysts
    Bradford, MCJ
    Vannice, MA
    [J]. JOURNAL OF CATALYSIS, 1998, 173 (01) : 157 - 171
  • [4] High carbon-resistance Ni/CeAlO3-Al2O3 catalyst for CH4/CO2 reforming
    Chen, Wei
    Zhao, Guofeng
    Xue, Qingsong
    Chen, Li
    Lu, Yong
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2013, 136 : 260 - 268
  • [5] Choudhary VR, 1998, J CHEM TECHNOL BIOT, V73, P345, DOI 10.1002/(SICI)1097-4660(199812)73:4<345::AID-JCTB961>3.0.CO
  • [6] 2-#
  • [7] Catalytic Technology for Carbon Dioxide Reforming of Methane to Synthesis Gas
    Fan, Mun-Sing
    Abdullah, Ahmad Zuhairi
    Bhatia, Subhash
    [J]. CHEMCATCHEM, 2009, 1 (02) : 192 - 208
  • [8] Gil A. L., 2008, J MOL CATAL A-CHEM, V281, P207
  • [9] Effects of Processing Conditions on the Work Function and Energy-Level Alignment of NiO Thin Films
    Greiner, Mark T.
    Helander, Michael G.
    Wang, Zhi-Bin
    Tang, Wing-Man
    Lu, Zheng-Hong
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (46) : 19777 - 19781
  • [10] Efficient Visible Light Photocatalytic CO2 Reforming of CH4
    Han, Bing
    Wei, Wei
    Chang, Liang
    Cheng, Peifu
    Hu, Yun Hang
    [J]. ACS CATALYSIS, 2016, 6 (02): : 494 - 497