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Methane decomposition into COx free hydrogen and multiwalled carbon nanotubes over ceria, zirconia and lanthana supported nickel catalysts prepared via a facile solid state citrate fusion method

机译:通过简便的固态柠檬酸盐熔融方法制备的二氧化铈,氧化锆和氧化镧负载的镍催化剂上的甲烷分解为无COx的氢和多壁碳纳米管

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Methane decomposition is the most effective route for the simultaneous production of COx-free hydrogen and nanocarbon. In this work, a set of porous ceria, zirconia and lanthana supported nickel catalysts were successfully synthesized via a facile solid state citrate fusion method and used for the thermocatalytic decomposition of undiluted methane for the first time. The catalysts were completely characterized for their crystalline, structural, textural and reduction properties and correlated to their catalytic performance. The active phase of fresh catalysts was found to be NiO in the CeO2 and ZrO2 supported catalysts whereas the formation of lanthanum nickel oxide solid solution was observed in the Ni/La2O3 catalyst. Various attractive porous morphologies of the fresh catalysts were confirmed by scanning electron microscopic studies. All of the catalysts exhibited high catalytic activity and stability for methane decomposition. The yield of hydrogen and carbon increased significantly with increasing the reaction temperature from 600 degrees C to 700 degrees C. A maximum initial hydrogen yield of 62%, 61% and 58% and a final carbon yield of 1360 wt%, 1159 wt% and 1576 wt% was achieved over ceria, zirconia and lanthana supported catalysts respectively, at 700 degrees C. The surface area of the catalysts could not have any significant effect on the catalytic efficiency and it was fully depended on the metal support interaction. The Ni/La2O3 catalyst showed high catalytic stability than ceria and zirconia supported catalysts due to the enhanced surface dispersion of finely crystallized Ni nanoparticles on the lanthana matrix aroused by the reduction of lanthanum nickel oxide. Moreover, bulk deposition of highly uniform multiwalled carbon nanotubes with high graphitization degree (I-D/I-G = 0.95) with different diameters depending on the Ni crystalline size was observed over the catalysts. (C) 2016 Elsevier Ltd. All rights reserved.
机译:甲烷分解是同时生产不含COx的氢和纳米碳的最有效途径。在这项工作中,通过一种简便的固态柠檬酸盐熔融方法成功地合成了一组多孔的氧化铈,氧化锆和氧化镧负载的镍催化剂,并将其首次用于未稀释甲烷的热催化分解。催化剂的结晶,结构,质构和还原性能均得到了全面表征,并与其催化性能相关。发现在CeO2和ZrO2负载的催化剂中新鲜催化剂的活性相为NiO,而在Ni / La2O3催化剂中观察到镧镍氧化物固溶体的形成。通过扫描电子显微镜研究证实了新鲜催化剂的各种有吸引力的多孔形态。所有催化剂均显示出高催化活性和甲烷分解稳定性。随着反应温度从600摄氏度增加到700摄氏度,氢和碳的产率显着增加。最大初始氢产率为62%,61%和58%,最终碳产率为1360 wt%,1159 wt%和在700℃下,分别在二氧化铈,氧化锆和氧化镧负载的催化剂上达到了1576wt%。催化剂的表面积对催化效率没有任何显着影响,并且完全取决于金属载体的相互作用。 Ni / La2O3催化剂显示出比二氧化铈和氧化锆负载的催化剂高的催化稳定性,这是由于细晶的Ni纳米颗粒在氧化镧镧还原引起的氧化镧基质上的表面分散性增强。此外,在催化剂上观察到具有高石墨化度(I-D / I-G = 0.95),具有不同直径的高均匀度的多壁碳纳米管的整体沉积,所述直径取决于Ni的晶体尺寸。 (C)2016 Elsevier Ltd.保留所有权利。

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