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CO2 Reforming of CH4 over Nickel and Cobalt Catalysts Prepared from La-Based Perovskite Precursors

机译:La基钙钛矿前体制备的镍和钴催化剂上的CH4 CO2重整

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摘要

Four perovskite-type complex oxides (LaNiO3, La2NiO4, LaCoO3 and La2CoO4) were suc-cessfully prepared using two sol-gel methods, the Pechini method (PC) and the citric acid complexingmethod (CC). The catalysts were characterized by XRD and TPR. After reduction, the activity of thecatalysts in the CO2 reforming of methane was tested. Ni-based catalysts from La2NiO4 precursors werethe most active and stable catalyst after calcination above 850 ℃, which gave a methane conversion of0.025 mmol/(g@s) for those prepared by the PC method and 0.020 mmol/(g.s) by the CC method. Itwas proposed that the well-defined structure and lower reducibility is responsible for the unusual catalyticbehavior observed over the pre-reduced La2NiO4 catalyst.
机译:使用两种溶胶-凝胶法(Pechini法(PC)和柠檬酸络合法(CC))成功制备了四种钙钛矿型复合氧化物(LaNiO3,La2NiO4,LaCoO3和La2CoO4)。通过XRD和TPR对催化剂进行了表征。还原后,测试了催化剂在甲烷CO2重整中的活性。在850℃以上煅烧后,La2NiO4前驱体的镍基催化剂是活性最稳定的催化剂,PC法制备的甲烷转化率为0.025 mmol /(g @ s),PC法制备的甲烷转化率为0.020 mmol /(gs)。 CC方法。有人提出,良好的结构和较低的还原性是导致在预还原的La2NiO4催化剂上观察到的异常催化行为的原因。

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