制备用于乙炔选择性加氢的核壳 Ni/CeO2@Al2O3 催化剂

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Zhichao Na , Liuyi Pan , Hedan Yao , Liang Chen , Yanhui Liu , Jiaojiao Liu , Zihao Tao , Dong Li , Wenhong Li
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引用次数: 0

摘要

核壳结构的晶格应变和配体效应可调节催化剂表面活性金属的几何和电子特性。本文采用水热沉积法制备了一种核壳 Ni/CeO2@Al2O3 催化剂,用于乙炔的选择性加氢反应。与一般的 Ni/Al2O3 催化剂相比,Ni/CeO2@Al2O3 催化剂的乙烯选择性显著提高,原因在于其特殊的结构降低了对乙烯的吸附强度。在 CeO2 加载 10% 的条件下,催化剂的性能最好(C2H2 转化率为 85.3%,C2H4 选择性为 81.2%)。这项工作为探索半加氢反应的高效催化剂提供了一种新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preparation of core-shell Ni/CeO2@Al2O3 catalyst for selective hydrogenation of acetylene

Preparation of core-shell Ni/CeO2@Al2O3 catalyst for selective hydrogenation of acetylene

Preparation of core-shell Ni/CeO2@Al2O3 catalyst for selective hydrogenation of acetylene

Lattice strain and ligand effects of core-shell structure regulate the geometric and electronic properties of the active metal on the surface of catalysts. Herein, a core-shell Ni/CeO2@Al2O3 catalyst was prepared by hydrothermal deposition for selective hydrogenation of acetylene. Compared with the general Ni/Al2O3 catalyst, the ethylene selectivity of the Ni/CeO2@Al2O3 catalyst was significantly improved due to the special structure reduced the adsorption strength of ethylene. Under the condition of 10% CeO2 loading, the performance of the catalyst was the best (85.3% C2H2 conversion and 81.2% C2H4 selectivity). This work provided a new approach for exploring efficient catalysts for semi‑hydrogenation reaction.

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来源期刊
Catalysis Communications
Catalysis Communications 化学-物理化学
CiteScore
6.20
自引率
2.70%
发文量
183
审稿时长
46 days
期刊介绍: Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results homogeneous, heterogeneous, and enzymatic catalysis.
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