Influence of Microwave Irradiation on Precursor Microstructure and Catalytic Performance of Cu/ZnO/Al2O3 for Slurry Methanol Synthesis

被引:6
作者
Li Zhong [1 ]
Fan Hui [1 ]
Zheng Huayan [1 ]
Liu Yan [1 ]
机构
[1] Taiyuan Univ Technol, Minist Educ & Shanxi Prov, Key Lab Coal Sci & Technol, Taiyuan 030024, Shanxi, Peoples R China
关键词
microwave irradiation; aging temperature; methanol synthesis; slurry reactor; copper; zinc oxide; alumina; LIQUID-PHASE METHANOL; CUO/ZNO/AL2O3; CATALYST; OXIDE CATALYSTS; DEACTIVATION; ZNO; CU; TEMPERATURE;
D O I
10.3724/SP.J.1088.2010.91025
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Microwave irradiation was used in the aging process for the preparation of the Cu/ZnO/Al2O3 catalyst precursor, and the effect of aging temperature on the catalyst precursor structure and catalytic properties for slurry methanol synthesis was studied. The characterization by X-ray diffraction, FT-IR spectroscopy, derivative thermogravimetry, H-2 temperature-programmed reduction, X-ray photoelectron spectroscopy, transmission electron microscopy, and particle size analysis showed that the microwave irradiation during the aging process promoted the substitution of Zn2+ in Zn-5(CO3)(2)(OH)(6) compound by Cu2+ and increased the content of (Cu,Zn)(5)(CO3)(2)(OH)(6) phase in the precursor. The calcined catalyst had strong interaction between CuO and ZnO, well dispersed CuO crystal particles, and high surface CuO content. The Cu/ZnO/Al2O3 catalyst aged at 80 under microwave irradiation exhibited the highest methanol space-time yield (STY) and more stable catalytic activity. Compared with the catalyst prepared without microwave irradiation, the methanol STY and deactivation rate of the catalyst aged at 80 degrees C under microwave irradiation were increased and decreased by 10.1% and 31.2%, respectively.
引用
收藏
页码:471 / 478
页数:8
相关论文
共 34 条
[11]   Spectroscopic evidence of Cu-Al interactions in Cu-Zn-Al mixed oxide catalysts used in CO hydrogenation [J].
Figueiredo, RT ;
Martinez-Arias, A ;
Granados, ML ;
Fierro, JLG .
JOURNAL OF CATALYSIS, 1998, 178 (01) :146-152
[12]   The chemical modification seen in the Cu/ZnO methanol synthesis catalysts [J].
Fujitani, T ;
Nakamura, J .
APPLIED CATALYSIS A-GENERAL, 2000, 191 (1-2) :111-129
[13]   Synthesis of ZnO with and without microwaves [J].
Komarneni, S ;
Bruno, M ;
Mariani, E .
MATERIALS RESEARCH BULLETIN, 2000, 35 (11) :1843-1847
[14]   Liquid phase methanol and dimethyl ether synthesis from syngas [J].
Lee, SG ;
Sardesai, A .
TOPICS IN CATALYSIS, 2005, 32 (3-4) :197-207
[15]   Characterization of precursors of methanol synthesis catalysts, copper zinc aluminum oxides, precipitated at different pHs and temperatures [J].
Li, JL ;
Inui, T .
APPLIED CATALYSIS A-GENERAL, 1996, 137 (01) :105-117
[16]  
Li Z, 2008, CHINESE J CATAL, V29, P431
[17]  
Li Z, 2009, CHEM J CHINESE U, V30, P2215
[18]   Structure and activity of microwave irradiated silica supported Pd-Fe bimetallic catalysts in the hydrodechlorination of chlorobenzene [J].
Lingaiah, N ;
Prasad, PSS ;
Rao, PK ;
Berry, FJ ;
Smart, LE .
CATALYSIS COMMUNICATIONS, 2002, 3 (09) :391-397
[19]   Characterization of precursors to methanol synthesis catalysts Cu/ZnO system [J].
Millar, GJ ;
Holm, IH ;
Uwins, PJR ;
Drennan, J .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1998, 94 (04) :593-600
[20]   Comparative study of Cu/ZnO catalysts derived from different precursors as a function of aging [J].
Muhamad, E. N. ;
Irmawati, R. ;
Tautiq-Yap, Y. H. ;
Abdullah, A. H. ;
Kniep, B. L. ;
Girgsdies, F. ;
Ressler, T. .
CATALYSIS TODAY, 2008, 131 (1-4) :118-124