Trend and Progress in Catalysis for Ethylene Production from Bioethanol Using ZSM-5

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-11-11 DOI:10.1021/acscatal.4c04162
L. Ouayloul, I. Agirrezabal-Telleria, Paul Sebastien, M. El Doukkali
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Abstract

Advancing technologies for the conversion of bioethanol (ET) to ethylene (ETY) holds significant potential for enhancing the production of numerous tertiary chemicals, which are currently derived from fossil-based resources. This review explores the feasibility of producing ethylene from bioethanol and underscores its growing importance in the global market. It focuses on breakthroughs in ZSM-5-based catalysts, compared to conventional ones, with particular attention to two key aspects: (i) the remodulation of ZSM-5 properties to establish a clear catalyst structure–reactivity–selectivity relationship in ET conversion and (ii) the identification of major factors influencing ZSM-5 stability and reusability. State-of-the-art approaches for ZSM-5 modification and regeneration are thoroughly examined with an emphasis on the role of active sites in ETY formation. The impact of key reaction parameters (such as temperature, space velocity, pressure, and feed composition (including impurities and water)) on ET-to-ETY reaction kinetics is systematically evaluated. The review shows that the formation of undesirable C3+ hydrocarbons is promoted by the contribution of strong Brønsted acid sites at elevated temperatures. In contrast, pathways favoring the formation of ETY or diethyl ether (DEE) are driven by the individual or synergistic effects of weak Lewis and strong Brønsted acid sites at milder temperatures. The integration of ET-to-ETY conversion within compact biorefineries and polyolefin manufacturing chains, alongside in situ regeneration of ZSM-5 catalysts through controlled cofeeding of H2O at moderate temperatures, presents a promising strategy for intensifying the ET-to-ETY process. This Perspective expects to provide a comprehensive overview of recent developments in ET-to-ETY catalysis, particularly at lower temperatures, with the goal of improving process efficiency in terms of energy consumption, cost, and CO2 emissions.

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利用 ZSM-5 催化生物乙醇生产乙烯的趋势与进展
生物乙醇(ET)转化为乙烯(ETY)技术的不断进步,为提高众多三级化学品的生产带来了巨大潜力,而这些化学品目前都来自化石资源。本综述探讨了利用生物乙醇生产乙烯的可行性,并强调了其在全球市场中日益增长的重要性。与传统催化剂相比,本综述重点介绍基于 ZSM-5 的催化剂取得的突破,并特别关注两个关键方面:(i) ZSM-5 性能的重塑,以便在 ET 转化过程中建立明确的催化剂结构-反应活性-选择性关系;(ii) 确定影响 ZSM-5 稳定性和可重复使用性的主要因素。对 ZSM-5 改性和再生的最新方法进行了深入研究,重点是活性位点在 ETY 形成中的作用。系统评估了关键反应参数(如温度、空间速度、压力和进料成分(包括杂质和水))对 ET-to-ETY 反应动力学的影响。研究结果表明,在高温条件下,强勃氏酸位点会促进不良 C3+ 碳氢化合物的形成。相反,在较温和的温度下,弱路易斯酸位点和强布伦斯特酸位点的单独或协同作用会推动 ETY 或二乙醚 (DEE) 的形成。在紧凑型生物炼油厂和聚烯烃生产链中整合 ET 到ETY 的转化过程,同时通过在温和温度下控制 H2O 的共进料实现 ZSM-5 催化剂的原位再生,为强化 ET 到ETY 的转化过程提供了一种前景广阔的策略。本视角将全面概述 ET 转ETY 催化技术的最新发展,尤其是在较低温度下的发展,目的是在能耗、成本和二氧化碳排放方面提高工艺效率。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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