首页> 外文期刊>Journal of Catalysis >Elementary reactions in the oxidative coupling of methane over Mn/Na2WO4/SiO2 and Mn/Na2WO4/MgO catalysts
【24h】

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

机译:Mn / Na2WO4 / SiO2和Mn / Na2WO4 / MgO催化剂上甲烷氧化偶联中的基本反应

获取原文
获取原文并翻译 | 示例
       

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. [References: 18]
机译:尽管在800°C的条件下,在Mn / Na2WO4 / SiO2和Mn / Na2WO4 / MgO催化剂上CH4(OCM)的氧化偶联过程中,可以实现20%的CH4转化率和80%的C2 +选择性,但这些材料的活性大大低于Sr / La2O3催化剂。同样,SiO2和MgO基催化剂在CH3的形成中活性较低。自由基发散到气相中以及这些自由基与催化剂的二次反应中。在OCM反应过程中,乙烷是主要产物。在短的接触时间内仅少量生产乙烯。然而,作为副产物,乙烯与甲烷竞争形成二氧化碳。由于CH4对气相氧化反应的抑制作用,在800摄氏度下C2H4向CO2的转化主要是异质反应的结果。脉冲实验表明,气相O-2的存在对于获得活性催化剂至关重要。据推测,涉及O-2的吸热平衡反应导致表面氧的形式,该表面氧能够从CH4中提取氢原子。 ca的异常大的活化能。两种催化剂的63 kcal / mol可能部分是由于这种氧平衡引起的。 (C)1998年学术出版社。 [参考:18]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号