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溶剂热法制备的NiO纳米颗粒和微米颗粒——用于CO甲烷化的惊人催化剂

NiO Nano- and Microparticles Prepared by Solvothermal Method-Amazing Catalysts for CO Methanation.

作者信息

Bikbashev Arkadii, Stryšovský Tomáš, Kajabová Martina, Kovářová Zuzana, Prucek Robert, Panáček Aleš, Kašlík Josef, Fodor Tamás, Cserháti Csaba, Erdélyi Zoltán, Kvítek Libor

机构信息

Department of Physical Chemistry, Faculty of Science, Palacky University Olomouc, 17. listopadu 12, CZ-77146 Olomouc, Czech Republic.

Czech Advanced Technology & Research Institute CATRIN, Regional Centrum of Advanced Technologies & Materials, Palacký University Olomouc, Slechtitelu 27, CZ-78371 Olomouc, Czech Republic.

出版信息

Molecules. 2024 Oct 12;29(20):4838. doi: 10.3390/molecules29204838.

Abstract

Nickel oxide (NiO) is one of the most popular hydrogenation catalysts. In heterogeneous catalysis, nickel oxide is used, for example, as a suitable methanation catalyst in the Fischer-Tropsch reaction not only for CO hydrogenation but also in the modified Fischer-Tropsch reaction with CO. However, CH selectivity and CO conversion strongly depend on NiO micro- (MPs) and nanoparticles' (NPs) shape, size, and surface area. In this study, the synthesis of NiO micro- and nanoparticles was conducted using the simple solvothermal method. Different morphologies (microspheres, sheet clusters, hexagonal microparticles, and nanodiscs) were prepared using this method with different solvents and stabilizers. The prepared catalysts were tested in the hydrogenation of CO in a gas phase with excellent conversion values and high selectivity to produce CH. The best results were obtained with the NiO with disc or sphere morphology, which produced methane with selectivity at a level near 100% and conversion close to 90%.

摘要

氧化镍(NiO)是最常用的氢化催化剂之一。在多相催化中,氧化镍被用作例如费托反应中合适的甲烷化催化剂,不仅用于一氧化碳氢化,也用于与一氧化碳的改进费托反应。然而,CH选择性和CO转化率强烈依赖于氧化镍微米颗粒(MPs)和纳米颗粒(NPs)的形状、尺寸和表面积。在本研究中,采用简单的溶剂热法合成了氧化镍微米颗粒和纳米颗粒。使用该方法并通过不同的溶剂和稳定剂制备了不同的形态(微球、片状聚集体、六边形微粒和纳米盘)。所制备的催化剂在气相CO氢化反应中进行了测试,具有优异的转化率值和对CH生成的高选择性。具有盘状或球状形态的氧化镍取得了最佳结果,其甲烷生成选择性接近100%,转化率接近90%。

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