Title of article :
Promotion effects of an extremely low concentration of noble metals supported onto Bi2Mo3O12 on the partial oxidation of iso-butane Original Research Article
Author/Authors :
Y. Takita، نويسنده , , S. Yoshida، نويسنده , , K. Usami، نويسنده , , T. Sato، نويسنده , , Y. Obana، نويسنده , , M. Ito، نويسنده , , M. Ogura، نويسنده , , H. Nishiguchi، نويسنده , , T. Ishihara، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2002
Pages :
7
From page :
215
To page :
221
Abstract :
Supporting extremely small concentrations of noble metals on SiO2 and Bi2Mo3O12 affected the catalytic activity and product distribution in iso-butane partial oxidation. Supporting Pt, Pd, and Rh onto SiO2 by 1 atom/μm2 enhanced the catalytic activity. Selectivity values of partial oxidation products, iso-butene, CH3C(CH3)CHO, CH3CHO and CH3COCH3, were increased and COx selectivity was decreased. Rh/SiO2 gave an EPR signal due to isolated Rh2+ ions with g⊥=2.07 and g∥=1.95, suggesting that two valent Rh ions are well dispersed on the surface and play a role in the oxidation of iso-butane. Supporting Pd, Ir, Rh, and Au onto Bi2Mo3O12 at a concentration of (1/9)×10−4 atom/nm2 increased the conversion, but supporting Pt and Ru decreased it. Selectivity values of CH2C(CH3)CHO and COx were the same for every catalyst. Catalytic activity was increased by supporting them by (1/49)×10−4 atom/nm2; especially, supporting Rh increased the activity without changing the selectivity of CH2C(CH3)CHO. Supported noble metal will interact with active oxygen ions bridging Mo and Bi on the Bi2Mo3O12 surface. Since a certain concentration of supported noble metals, (1/49)×10−4 nm2, begins to affect the catalytic activity and selectivity, this concentration may reflect the concentration of active sites in iso-butane oxidation at 350–400 °C over Bi2Mo3O12.
Keywords :
iso-Butane , Bi2Mo3O12 , Noble metal , Promotion effect , Oxidative dehydrogenation
Journal title :
Applied Catalysis A:General
Serial Year :
2002
Journal title :
Applied Catalysis A:General
Record number :
1155031
Link To Document :
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