An evidence of active surface MoOx over MgMoO4 for the catalytic oxidative dehydrogenation of propane

被引:41
作者
Lee, KH
Yoon, YS
Ueda, W
Morooka, Y
机构
[1] TOKYO INST TECHNOL,RESOURCES UTILIZAT RES LAB,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
[2] TOKYO INST TECHNOL,DEPT ENVIRONM CHEM & ENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
关键词
metal molybdate; MoOx clusters; oxidative dehydrogenation; propane; acidic property;
D O I
10.1023/A:1019047324930
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
In order to clarify whether MgMoxOy catalysts with slight excess of molybdenum relative to the stoichiometric MgMoO4 compound showed increased activities for propene formation in the propane oxidative dehydrogenation, we investigated the catalytic properties of MoO3 supported on MgMoO4 and of MgMoxOy catalysts treated with acid or base. Supporting MoO3 on magnesium-rich MgMo0.99Oy catalysts which are poorly active, or treating them with acetic acid to remove excess magnesium, resulted in drastic activity increases. On the other hand, the ammonia treatment of molybdenum-rich MgMo1.05Oy, catalysts which are highly active turned out to give a remarkable decrease in activity, because surface MoOx dissolved in ammonia water. A clear correlation was observed between the catalytic activities for propane oxidation and the dehydration of 2-propanol to propene over the supported catalyst and the treated catalysts. Since the bulk structures were unchanged by supporting or by the treatments, the existence of MoOx clusters formed on the surface of MgMoO4 are responsible for the activities in the oxidative dehydrogenation of propane.
引用
收藏
页码:267 / 271
页数:5
相关论文
共 12 条
[1]   Oxidative dehydrogenation of of propane over molybdenum supported on MgO-gamma-Al2O3 [J].
Abello, MC ;
Gomez, MF ;
Cadus, LE .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (07) :2137-2143
[2]  
ABELLO MC, 1997, CATAL LETT, V43, P229
[3]   Oxidative dehydrogenation of propane over Mg-Mo-O catalysts [J].
Cadus, LE ;
Abello, MC ;
Gomez, MF ;
Rivarola, JB .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (01) :14-18
[4]  
CIYRCIT D, 1993, J CHEM SOC FARADAY T, V92, P1609
[5]   Oxidative dehydrogenation of light (C-2 to C-4) alkanes [J].
Kung, HH .
ADVANCES IN CATALYSIS, VOL 40, 1994, 40 :1-38
[6]   SELECTIVITY PATTERNS IN ALKANE OXIDATION OVER MG3(VO4)2-MGO, MG2V2O7, AND (VO)2P2O7 [J].
MICHALAKOS, PM ;
KUNG, MC ;
JAHAN, I ;
KUNG, H .
JOURNAL OF CATALYSIS, 1993, 140 (01) :226-242
[7]  
MOROOKA Y, 1994, CATALYSIS, V11, P223
[8]   Role of the nature of the acid sites in the oxydehydrogenation of propane on a VPO/TiO2 catalyst. An in situ FT-IR spectroscopy investigation [J].
Savary, L ;
Saussey, J ;
Costentin, G ;
Bettahar, MM ;
Lavalley, JC ;
GubelmannBonneau, M .
CATALYSIS LETTERS, 1996, 38 (3-4) :197-201
[9]   OXIDATIVE DEHYDROGENATION OF PROPANE TO PROPENE OVER COBALT MOLYBDATE CATALYSTS [J].
YOON, YS ;
FUJIKAWA, N ;
UEDA, W ;
MOROOKA, Y .
CHEMISTRY LETTERS, 1994, (09) :1635-1636
[10]   PROPANE OXIDATION OVER VARIOUS METAL MOLYBDATE CATALYSTS [J].
YOON, YS ;
FUJIKAWA, N ;
UEDA, W ;
MOROOKA, Y ;
LEE, KW .
CATALYSIS TODAY, 1995, 24 (03) :327-333