Microwave-hydrothermal synthesis and characterization of nanostructured copper substituted ZnM2O4 (M = Al, Ga) spinels as precursors for thermally stable Cu catalysts

被引:32
|
作者
Conrad, Franziska [1 ]
Massue, Cyriac [2 ,3 ]
Kuehl, Stefanie [2 ]
Kunkes, Edward [2 ]
Girgsdies, Frank [2 ]
Kasatkin, Igor [2 ]
Zhang, Bingsen [2 ]
Friedrich, Matthias [4 ]
Luo, Yuan [4 ]
Armbruester, Marc [4 ]
Patzke, Greta R. [1 ]
Behrens, Malte [2 ]
机构
[1] Univ Zurich, Inst Inorgan Chem, CH-8057 Zurich, Switzerland
[2] Max Planck Gesell, Fritz Haber Inst, Dept Inorgan Chem, D-14195 Berlin, Germany
[3] Ecole Polytech Paris Tech, F-91128 Palaiseau, France
[4] Max Planck Inst Chem Phys Fester Stoffe, D-01187 Dresden, Germany
基金
瑞士国家科学基金会;
关键词
ZINC-OXIDE CATALYSTS; METHANOL SYNTHESIS; CU/ZNO/AL2O3; CATALYSTS; STRUCTURAL-CHANGES; DEFECT FORMATION; HYDROGEN; PERFORMANCE; DECOMPOSITION; CHEMISORPTION; DEACTIVATION;
D O I
10.1039/c2nr11804a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanostructured CuxZn1-xAl2O4 with a Cu : Zn ratio of 1/4 : 3/4 has been prepared by a microwave-assisted hydrothermal synthesis at 150 degrees C and used as a precursor for Cu/ZnO/Al2O3-based catalysts. The spinel nanoparticles exhibit an average size of approximately 5 nm and a high specific surface area (above 250 m(2) g(-1)). Cu nanoparticles of an average size of 3.3 nm can be formed by reduction of the spinel precursor in hydrogen and the accessible metallic Cu(0) surface area of the reduced catalyst was 8 m(2) g(-1). The catalytic performance of the material in CO2 hydrogenation and methanol steam reforming was compared with conventionally prepared Cu/ZnO/Al2O3 reference catalysts. The observed lower performance of the spinel-based samples is attributed to a lack of synergetic interaction of the Cu nanoparticles with ZnO due to the incorporation of Zn2+ in the stable spinel lattice. Despite its lower performance, however, the nanostructured nature of the spinel catalyst was stable after thermal treatment up to 500 degrees C in contrast to other Cu-based catalysts. Furthermore, a large fraction of the re-oxidized copper migrates back into the spinel upon calcination of the reduced catalyst, thereby enabling a regeneration of sintered catalysts after prolonged usage at high temperatures. Similarly prepared samples with Ga instead of Al exhibit a more crystalline catalyst with a spinel particle size around 20 nm. The slightly decreased Cu(0) surface area of 3.2 m(2) g(-1) due to less copper incorporation is not a significant drawback for the methanol steam reforming.
引用
收藏
页码:2018 / 2028
页数:11
相关论文
共 5 条
  • [1] Dimethyl ether synthesis on the admixed catalysts of Cu-Zn-Al-M (M = Ga, La, Y, Zr) and γ-Al2O3: The role of modifier
    Venugopal, Akula
    Palgunadi, Jelliarko
    Deog, Jung Kwang
    Joo, Oh-Shim
    Shin, Chae-Ho
    JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2009, 302 (1-2) : 20 - 27
  • [2] Effect of Copper Precursors to the Activity for Dimethyl Ether Synthesis from Syngas over Cu-ZnO/γ-Al2O3 Bifunctional Catalysts
    Baek, Seung-Chan
    Kang, Suk-Hwan
    Bae, Jong Wook
    Lee, Yun-Jo
    Lee, Dong-Hyun
    Lee, Kwan-Young
    ENERGY & FUELS, 2011, 25 (06) : 2438 - 2443
  • [3] Characterization and performance of Cu/ZnO/Al2O3 catalysts prepared via decomposition of M(Cu,Zn)-ammonia complexes under sub-atmospheric pressure for methanol synthesis from H2 and CO2
    Wang, Danjun
    Zhao, Jun
    Song, Huanling
    Chou, Lingjun
    JOURNAL OF NATURAL GAS CHEMISTRY, 2011, 20 (06): : 629 - 634
  • [4] Characterization and performance of Cu/ZnO/Al2O3 catalysts prepared via decomposition of M(Cu,Zn)-ammonia complexes under sub-atmospheric pressure for methanol synthesis from H2 and CO2
    Danjun Wang1
    2.Graduate School of Chinese Academy of Sciences
    Journal of Natural Gas Chemistry , 2011, (06) : 629 - 634
  • [5] Sucrose-aided combustion synthesis of nanosized LiMn1.99-yLiyM0.01O4 (M = Al3+, Ni2+, Cr3+, Co3+, y=0.01 and 0.06) spinels Characterization and electrochemical behavior at 25 and at 55 °C in rechargeable lithium cells
    Amarilla, J. M.
    Petrov, K.
    Pico, F.
    Avdeev, G.
    Rojo, J. M.
    Rojas, R. M.
    JOURNAL OF POWER SOURCES, 2009, 191 (02) : 591 - 600