首页> 外文期刊>International journal of hydrogen energy >Effect of combining Al, Mg, Ce or La oxides to extracted rice husk nanosilica on the catalytic performance of NiO during COX-free hydrogen production via methane decomposition
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Effect of combining Al, Mg, Ce or La oxides to extracted rice husk nanosilica on the catalytic performance of NiO during COX-free hydrogen production via methane decomposition

机译:Al,Mg,Ce或La氧化物与提取的稻壳纳米二氧化硅混合使用对甲烷分解过程中无COX产氢中NiO催化性能的影响

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Amorphous nanosilica powder was extracted from rice husk and used as a catalyst support as well as a starting material for the preparation of different binary oxides, i.e., SiO2 Al2O3, SiO2 MgO, SiO2-CeO2 and SiO2 La2O3. A series of supported nickel catalysts with the metal loading of 50 wt % were prepared by wet impregnation method and evaluated in methane decomposition to "COx -free" hydrogen production. The fresh and spent catalysts were extensively characterized by different techniques. Among the evaluated catalysts, both Ni/SiO2 Al2O3 and Ni/SiO2 La2O3 catalysts were the most active with an over-all H-2 yield of ca. 80% at the initial period of the reaction. This distinguishable higher catalytic activity is mainly referred to the presence of free mobile surface NiO and/or that NiO fraction weakly interacted with the support easily reducible at low temperatures. The Ni/ SiO2-CeO2 catalyst has proven a great potential for application in the hydrogen production in terms of its catalytic stability. The formation of MgxNi(1-x)O solid solution caused the Ni/ SiO2-MgO catalyst to lose its activity and stability at a long reaction time. Various types of carbon materials were formed on the catalyst surface depending on the type of support used. TEM images of as -deposited carbon showed that multi-walled carbon nanotubes (MWCNTs) and graphene platelets were formed on Ni/SiO2, while only MWCNTs were deposited on all binary oxide supported Ni catalysts. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:从稻壳中提取无定形纳米二氧化硅粉并用作催化剂载体以及制备不同二元氧化物的起始原料,即SiO2 Al2O3,SiO2 MgO,SiO2-CeO2和SiO2 La2O3。通过湿法浸渍法制备了一系列负载量为50 wt%的负载型镍催化剂,并进行了甲烷分解以评估生成“无COx”氢的能力。用不同的技术广泛地表征了新鲜催化剂和废催化剂。在所评估的催化剂中,Ni / SiO2 Al2O3和Ni / SiO2 La2O3催化剂活性最高,H-2的总产率约为。反应初期为80%。这种可区分的较高的催化活性主要是指存在游离的可移动表面NiO和/或NiO组分与载体的弱相互作用,在低温下容易还原。 Ni / SiO2-CeO2催化剂就其催化稳定性而言,已被证明具有巨大的潜力可用于制氢。 MgxNi(1-x)O固溶体的形成导致Ni / SiO2-MgO催化剂在较长的反应时间内失去活性和稳定性。取决于所用载体的类型,各种类型的碳材料形成在催化剂表面上。沉积碳的TEM图像显示在Ni / SiO2上形成了多壁碳纳米管(MWCNT)和石墨烯片晶,而在所有二元氧化物负载的Ni催化剂上仅沉积了MWCNT。 (C)2017氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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