Bismuth Molybdate Catalysts Prepared by Mild Hydrothermal Synthesis: Influence of pH on the Selective Oxidation of Propylene

被引:40
作者
Schuh, Kirsten [1 ]
Kleist, Wolfgang [1 ,2 ]
Hoj, Martin [3 ]
Trouillet, Vanessa [4 ,5 ]
Beato, Pablo [6 ]
Jensen, Anker Degn [3 ]
Grunwaldt, Jan-Dierk [1 ,2 ]
机构
[1] Karlsruhe Inst Technol, Inst Chem Technol & Polymer Chem ITCP, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Catalysis Res & Technol IKFT, D-76344 Eggenstein Leopoldshafen, Germany
[3] Tech Univ Denmark DTU, Dept Chem & Biochem Engn, DK-2800 Lyngby, Denmark
[4] Karlsruhe Inst Technol, Inst Appl Mat, D-76344 Eggenstein Leopoldshafen, Germany
[5] Karlsruhe Inst Technol, KNMF, D-76344 Eggenstein Leopoldshafen, Germany
[6] Haldor Topsoe Res Labs, DK-2800 Lyngby, Denmark
关键词
hydrothermal synthesis; bismuth molybdate; effect of pH; propylene oxidation; acrolein; VANADIUM MOLYBDENUM OXIDE; FLAME SPRAY-PYROLYSIS; GAMMA-PHASE; PHOTOCATALYTIC ACTIVITY; RAMAN-SPECTROSCOPY; ALPHA-BISMUTH; MIXED OXIDES; BETA-PHASE; BI2MOO6; PROPENE;
D O I
10.3390/catal5031554
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of bismuth molybdate catalysts with relatively high surface area was prepared via mild hydrothermal synthesis. Variation of the pH value and Bi/Mo ratio during the synthesis allowed tuning of the crystalline Bi-Mo oxide phases, as determined by X-ray diffraction (XRD) and Raman spectroscopy. The pH value during synthesis had a strong influence on the catalytic performance. Synthesis using a Bi/Mo ratio of 1/1 at pH 6 resulted in -Bi2MoO6, which exhibited a better catalytic performance than phase mixtures obtained at lower pH values. However, a significantly lower catalytic activity was observed at pH = 9 due to the low specific surface area. -Bi2MoO6 synthesized with Bi/Mo = 1/1 at pH = 6 and 7 exhibited relatively high surface areas and the best catalytic performance. All samples prepared with Bi/Mo = 1/1, except samples synthesized at pH = 1 and 9, showed better catalytic performance than samples synthesized with Bi/Mo = 2/3 at pH = 4 and 9 and -Bi2MoO6 synthesized by co-precipitation at pH = 7. At temperatures above 440 degrees C, the catalytic activity of the hydrothermally synthesized bismuth molybdates started to decrease due to sintering and loss of surface area. These results support that a combination of the required bismuth molybdate phase and a high specific surface area is crucial for a good performance in the selective oxidation of propylene.
引用
收藏
页码:1554 / 1573
页数:20
相关论文
共 70 条
[1]   CATALYTIC PROPERTIES OF BI/MO OXIDE CATALYSTS PREPARED VIA PRECIPITATION [J].
ALESHINA, GI ;
JOSHI, C ;
TARASOVA, DV ;
KUSTOVA, GN ;
NIKORO, TA .
REACTION KINETICS AND CATALYSIS LETTERS, 1984, 26 (1-2) :203-208
[2]   X-ray photoelectron spectroscopic study on α- and γ-bismuth molybdate surfaces exposed to hydrogen, propene and oxygen [J].
Ayame, A ;
Uchida, K ;
Iwataya, M ;
Miyamoto, M .
APPLIED CATALYSIS A-GENERAL, 2002, 227 (1-2) :7-17
[3]  
BATIST PA, 1979, J CHEM TECHNOL BIOT, V29, P451
[4]   BISMUTH MOLYBDATE CATALYSTS - PREPARATION, CHARACTERIZATION AND ACTIVITY OF DIFFERENT COMPOUNDS IN BI-MO-O SYSTEM [J].
BATIST, PA ;
BOUWENS, JFH ;
SCHUIT, GCA .
JOURNAL OF CATALYSIS, 1972, 25 (01) :1-&
[5]   In situ study of the formation of crystalline bismuth molybdate materials under hydrothermal conditions [J].
Beale, AM ;
Sankar, G .
CHEMISTRY OF MATERIALS, 2003, 15 (01) :146-153
[6]   An iron molybdate catalyst for methanol to formaldehyde conversion prepared by a hydrothermal method and its characterization [J].
Beale, Andrew M. ;
Jacques, Simon D. M. ;
Sacaliuc-Parvalescu, Elena ;
O'Brien, Matthew G. ;
Barnes, Paul ;
Weckhuysen, Bert M. .
APPLIED CATALYSIS A-GENERAL, 2009, 363 (1-2) :143-152
[7]   Selective oxidative dehydrogenation of ethane on MoVTeNbO mixed metal oxide catalysts [J].
Botella, P ;
García-González, E ;
Dejoz, A ;
Nieto, JML ;
Vázquez, MI ;
González-Calbet, J .
JOURNAL OF CATALYSIS, 2004, 225 (02) :428-438
[8]   REDOX KINETICS OF BISMUTH MOLYBDATE AMMOXIDATION CATALYSTS [J].
BRAZDIL, JF ;
SURESH, DD ;
GRASSELLI, RK .
JOURNAL OF CATALYSIS, 1980, 66 (02) :347-367
[9]  
Briand G.G., 1999, THESIS DALHOUSIE U H
[10]  
CALLAHAN JL, 1962, Patent No. 3044966