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CO_2 Reforming of CH_4 over Nickel and Cobalt Catalysts Prepared from La-Based Perovskite Precursors

机译:镧基钙钛矿前驱体制备的镍钴催化剂上CH_4的CO_2重整

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摘要

Four perovskite-type complex oxides (LaNiO_3, La_2NiO_4, LaCoO_3 and La_2CoO_4) were successfully prepared using two sol-gel methods, the Pechini method (PC) and the citric acid complexing method (CC). The catalysts were characterized by XRD and TPR. After reduction, the activity of the catalysts in the CO_2 reforming of methane was tested. Ni-based catalysts from La_2NiO_4 precursors were the most active and stable catalyst after calcination above 850 ℃, which gave a methane conversion of 0.025 mmol/(g·s) for those prepared by the PC method and 0.020 mmol/(g·s) by the CC method. It was proposed that the well-defined structure and lower reducibility is responsible for the unusual catalytic behavior observed over the pre-reduced La2NiO_4 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(LaNiO_3,La_2NiO_4,LaCoO_3和La_2CoO_4)。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的CO_2重整中的活性。 La_2NiO_4前驱体的镍基催化剂是在850℃以上煅烧后活性最高,最稳定的催化剂,采用PC法制得的甲烷甲烷转化率为0.025 mmol /(g·s),而甲烷转化率为0.020 mmol /(g·s)通过CC方法。有人提出,良好的结构和较低的还原性是导致在预先还原的La2NiO_4催化剂上观察到的异常催化行为的原因。

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