Enhanced Ammonia Synthesis Performance over Ru-Based Catalysts via the Addition of Ce Promoter

IF 3.8 3区 工程技术 Q2 ENGINEERING, CHEMICAL
Tianhua Zhang, Kexin Yue, Jiangyang Mo, Mingyuan Zhang, Jie Zhu, Ruting Lin, Shiyong Zhang, Ruishao Mao, Yanliang Zhou, Jun Ni, Jianxin Lin, Xiuyun Wang, Lilong Jiang
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引用次数: 0

Abstract

The development of advanced catalysts is critical to realize efficient ammonia (NH3) synthesis under mild conditions. However, the activation of an inert N≡N bond in N2 molecules is the primary hindrance to NH3 synthesis, and hydrogen poisoning is another major and a serious problem, especially in Ru-based catalysts. Here, we develop an H-ZSM-5-supported Ru-based catalyst (Ce–Ru/HZ) via decorating with a CeO2 promoter to realize efficient NH3 synthesis. Our study shows that the Ce species can serve as an electron donor to enrich the electron density of Ru sites, thus accelerating N2 activation for NH3 synthesis. Meanwhile, the interaction of Ru and Ce can alleviate the effect of hydrogen poisoning on Ru sites. Consequently, the 16 wt % Ce-promoted Ru/HZ catalyst displays a superior NH3 synthesis rate and long-term stability of more than 550 h at 400 °C and 1 MPa.

Abstract Image

添加Ce促进剂提高ru基催化剂合成氨性能
先进催化剂的开发是实现温和条件下高效氨合成的关键。然而,N2分子中惰性N≡N键的激活是NH3合成的主要障碍,氢中毒是另一个主要和严重的问题,特别是在钌基催化剂中。本文采用CeO2促进剂修饰h - zsm -5负载的ru基催化剂(Ce-Ru /HZ),实现了NH3的高效合成。我们的研究表明,Ce可以作为电子供体来丰富Ru位点的电子密度,从而加速N2活化以合成NH3。同时,Ru和Ce的相互作用可以缓解氢中毒对Ru位点的影响。因此,16 wt % ce促进的Ru/HZ催化剂表现出优异的NH3合成速率和在400°C和1 MPa下超过550 h的长期稳定性。
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来源期刊
Industrial & Engineering Chemistry Research
Industrial & Engineering Chemistry Research 工程技术-工程:化工
CiteScore
7.40
自引率
7.10%
发文量
1467
审稿时长
2.8 months
期刊介绍: ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.
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