Zeolite catalysts for non-oxidative ethane dehydrogenation to ethylene

EES catalysis Pub Date : 2024-03-19 DOI:10.1039/D4EY00031E
Lu Liu, Liang Wang and Feng-Shou Xiao
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Abstract

The conversion of ethane to ethylene is crucial for deriving platform chemicals from non-petroleum feedstock. However, it currently relies on steam cracking technology, which involves high temperatures and large reactors. The catalytic dehydrogenation of ethane (EDH) could resolve these issues, but its efficiency is often limited due to thermodynamics, leading to low conversion and coke formation. These challenges make it difficult for catalytic EDH to compete economically with steam cracking. Recent studies show that rational design of catalysts, such as fixing metal nanoclusters within zeolite micropores or isolated metal sites on the zeolite framework, can enhance catalytic performances. These designs lower energy barriers for carbon–hydrogen bond activation, hinder deep dehydrogenation to coke, and provide sinter-resistant metal sites for durability. This review discusses the pivotal role of zeolite structures in catalysis and sums up the principles of catalyst design for efficient non-oxidative EDH. It aims to help in the development of more efficient zeolite catalysts and enhance the viability of catalytic EDH for potential industrialization.

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用于非氧化乙烷脱氢制乙烯的沸石催化剂
将乙烷转化为乙烯对于从非石油原料中提取平台化学品至关重要。然而,它目前依赖于蒸汽裂解技术,该技术涉及高温和大型反应器。乙烷催化脱氢(EDH)可以解决这些问题,但其效率往往因热力学而受到限制,导致转化率低和焦炭形成。这些挑战使得催化乙烷脱氢很难在经济上与蒸汽裂解竞争。最近的研究表明,催化剂的合理设计,如在沸石微孔中固定金属纳米团簇或在沸石框架上孤立金属位点,可以提高催化性能。这些设计降低了碳氢键活化的能量障碍,阻碍了焦炭的深度脱氢,并提供了耐烧结的金属位点以提高耐久性。本综述讨论了沸石结构在催化中的关键作用,并总结了高效非氧化脱氢催化剂的设计原则。其目的是帮助开发更高效的沸石催化剂,提高催化乙二醇加氢的可行性,以实现潜在的工业化。
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Back cover Correction: High photocatalytic yield in the non-oxidative coupling of methane using a Pd–TiO2 nanomembrane gas flow-through reactor Embedding the intermetallic Pt5Ce alloy in mesopores through Pt–C coordination layer interactions as a stable electrocatalyst for the oxygen reduction reaction† Efficient CO2-to-CO conversion in dye-sensitized photocatalytic systems enabled by electrostatically-driven catalyst binding† Green energy driven methane conversion under mild conditions
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