Elementary reactions in the oxidative coupling of methane over Mn/Na2WO4/SiO2 and Mn/Na2WO4/MgO catalysts

被引:169
作者
Pak, S [1 ]
Qiu, P [1 ]
Lunsford, JH [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
基金
美国国家科学基金会;
关键词
D O I
10.1006/jcat.1998.2228
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
Although it is possible to achieve 20% CH4 conversion and 80% C2+ selectivity during the oxidative coupling of CH4 (OCM) over Mn/Na2WO4/SiO2 and Mn/Na2WO4/MgO catalysts at 800 degrees C, these materials are considerably less active than a Sr/La2O3 catalyst. Similarly, the SiO2- and MgO-based catalysts are less active in the formation of CH3. radicals that emanate into the gas phase and in the secondary reaction of these radicals with the catalysts. During the OCM reaction, ethane is the primary product; ethylene is produced only in small amounts at short contact times. As a secondary product, however, ethylene competes with methane in the formation of carbon dioxide. The conversion of C2H4 to CO2 at 800 degrees C is largely a result of a heterogeneous reaction, due to the inhibiting effect of CH4 on the gas phase oxidation reaction. Pulse experiments demonstrated that the presence of gas phase O-2 is essential for obtaining an active catalyst. Presumably, an endothermic equilibrium reaction involving O-2 results in a form of surface oxygen that is capable of abstracting a hydrogen atom from CH4. The unusually large activation energy of ca. 63 kcal/mol for both catalysts may result, in part, from this oxygen equilibrium. (C) 1998 Academic Press.
引用
收藏
页码:222 / 230
页数:9
相关论文
共 18 条
[1]   GAS-PHASE COUPLING OF METHYL RADICALS DURING THE CATALYTIC PARTIAL OXIDATION OF METHANE [J].
CAMPBELL, KD ;
MORALES, E ;
LUNSFORD, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (25) :7900-7901
[2]   Steady-state production of olefins in high yields during the oxidative coupling of methane: Utilization of a membrane contactor [J].
Cordi, EM ;
Pak, S ;
Rosynek, MP ;
Lunsford, JH .
APPLIED CATALYSIS A-GENERAL, 1997, 155 (01) :L1-L7
[3]  
Fang X., 1992, J MOL CATALYSIS CHIN, V6, P427
[4]  
HUTCHINGS GJ, 1992, METHANE CONVERSION O, P201
[5]   OXIDE SUPPORT INTERACTION AND SURFACE RECONSTRUCTION IN THE NA2WO4/SIO2 SYSTEM [J].
JIANG, ZC ;
YU, CJ ;
FANG, XP ;
LI, SB ;
WANG, HL .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (49) :12870-12875
[6]   OXIDATIVE DIMERIZATION OF METHANE OVER SODIUM-PROMOTED CALCIUM-OXIDE [J].
LIN, CH ;
WANG, JX ;
LUNSFORD, JH .
JOURNAL OF CATALYSIS, 1988, 111 (02) :302-316
[7]   THE FORMATION OF GAS-PHASE PI-ALLYL RADICALS FROM PROPYLENE OVER BISMUTH OXIDE AND GAMMA-BISMUTH MOLYBDATE CATALYSTS [J].
MARTIR, W ;
LUNSFORD, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (13) :3728-3732
[8]   OXIDATIVE COUPLING OF METHANE FOLLOWED BY ETHANE PYROLYSIS [J].
MIMOUN, H ;
ROBINE, A ;
BONNAUDET, S ;
CAMERON, CJ .
CHEMISTRY LETTERS, 1989, (12) :2185-2188
[9]   OXIDATION OF C-2 HYDROCARBON PRODUCTS DURING THE OXIDATIVE COUPLING OF METHANE OVER A LI/MGO CATALYST [J].
NELSON, PF ;
CANT, NW .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (09) :3756-3761
[10]   Thermal effects during the oxidative coupling of methane over Mn/Na2WO4/SiO2 and Mn/Na2WO4/MgO catalysts [J].
Pak, S ;
Lunsford, JH .
APPLIED CATALYSIS A-GENERAL, 1998, 168 (01) :131-137