首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >In search of membrane-catalyst materials for oxidative coupling of methane: Performance and phase stability studies of gadolinium-doped barium cerate and the impact of Zr doping
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In search of membrane-catalyst materials for oxidative coupling of methane: Performance and phase stability studies of gadolinium-doped barium cerate and the impact of Zr doping

机译:寻找甲烷氧化偶联的膜催化剂材料:钆掺杂钡凝聚的性能和相位稳定性研究及ZR掺杂的影响

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Oxidative coupling of methane (OCM) is a promising technology for the direct conversion of methane to ethylene and ethane (C-2). This process is yet to be commercialized due its poor yield reflected in the formation of undesired products such as CO and CO2 (COx) as methane conversion increases, particularly in conventional packed bed reactors (PBRs). It has been argued that by applying O2- conducting membrane reactors that distribute the oxygen feed, the selectivity to the C-2 products can be increased. A practical design for these membrane reactors would include combining a selective catalyst, preferably O2- conducting, with an O2- conducting membrane. In this work, we studied an O2- conducting material, gadolinium-doped barium cerate (BaCe0.8Gd0.2O3-delta or BCG), to evaluate its potential applicability as a catalyst and membrane in OCM membrane reactors. From PBR tests, we found that this material was active for OCM, and achieved a maximum C2+ yield of similar to 14% at 1023 K. Furthermore, at low oxygen partial pressures, a C2+ selectivity of similar to 90% was obtained at methane conversions of similar to 3%. Although the C2+ yield from this material was stable over 48 h on stream at high methane conversions, X-ray diffraction data showed that the BCG perovskite phase, which is required for its conductive (membrane) properties, decomposes into BaCO3, CeO2 and Gd2O3 like phases, due to reactions with CO2. We showed that doping BCG with Zr was effective at suppressing the phase instability in OCM without significantly affecting the C2+ yields.
机译:甲烷(OCM)的氧化偶联是甲烷直接转化为乙烯和乙烷(C-2)的有希望的技术。由于甲烷转化率的不希望产品(如CO 2(COX)的形成,因此该方法尚未被商业化,因为甲烷转化增加,特别是在常规包装床反应器(PBR)中。已经认为,通过施加分布氧气进料的O 2导电膜反应器,可以增加对C-2产物的选择性。对于这些膜反应器的实际设计将包括将选择性催化剂,优选o2导电的选择性催化剂与O2导电膜组合。在这项工作中,我们研究了O 2导电材料,掺杂钆钡钡(Bace0.8GD0.2O3-Delta或BCG),以评估其在OCM膜反应器中作为催化剂和膜的潜在适用性。从PBR试验中发现,该材料对于OCM是活性的,并且在1023k时获得的最大C2 +产率与14%相似。此外,在低氧分压下,在甲烷转化下获得类似于90%的C2 +选择性与3%相似。虽然在高甲烷转化的高甲烷转化的流中,来自该材料的C2 +产率在48小时内稳定,但X射线衍射数据显示其导电(膜)性能所需的BCG钙钛矿相差分成Baco3,CeO2和Gd2O3。阶段,由于CO2的反应。我们表明,具有Zr的掺杂BCG在抑制OCM中的相稳定性,而不会显着影响C2 +产率。

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