Microwave-assisted ethanol dehydration to ethylene over biochar-based catalyst at low temperature†

IF 9.2 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Green Chemistry Pub Date : 2025-01-20 DOI:10.1039/d4gc05433d
Li Yang , Bonan Liu , Yingying Zhao , Zijian Zhang , Hanyu Wu , Minyi He , Chao Tang , Jun Zhao , Yu Fan , Wangjing Ma
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Abstract

Modern chemists dream of a low-temperature bioethanol dehydration to ethylene process promoted by biomaterial-based catalysts, which would be without doubt an energy-saving, sustainable achievement in green chemistry. However, limitations on catalytic activity and competition from exothermic side reactions have always been an insurmountable gap. Herein, a microwave-assisted pathway employing biochar-based catalysts was designed to effectively dehydrate ethanol into ethylene at temperatures lower than 100 °C. Either biochar (BC) or phosphoric acid-modified derivate (HBC) was synthesized from bamboo powder through a simple one-step decomposition. ZSM-5/MOR composite zeolite was further introduced to form HBC-2-ZSM-5/MOR hybrid catalysts, which could effectively prevent the formation of diethyl-ether and enhance the production of ethylene. With a microwave input power and reaction temperature as low as 10 W and 82 °C, ethanol (WHSV = 2 h−1) could be completely converted on the HBC-2-ZSM-5/MOR (1.5) catalyst with almost 100% ethylene selectivity. Similar results were obtained in the conversion of bioethanol (model), Chinese liquor and beer, pointing to the wide applicability of this strategy. Investigation of the potential mechanism found that weak acidity, special structure and P-modification characteristics can effectively inhibit the formation of diethyl ether by-products, oligomerization and the coking process, which is conducive to promoting the selective conversion of ethanol to ethylene. This work has blazed another trail for low-temperature ethanol to ethylene by combining the advantage of microwave heating with precise tailoring of biochar-based catalysts, all for a better future life with green chemistry.

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微波辅助乙醇脱水成乙烯在生物炭基催化剂在低温†
现代化学家梦想着用生物材料为基础的催化剂促进低温生物乙醇脱水制乙烯的过程,这无疑将是绿色化学中一项节能、可持续的成就。然而,对催化活性的限制和放热副反应的竞争一直是一个不可逾越的鸿沟。本文设计了一种微波辅助途径,采用生物炭基催化剂,在低于100°C的温度下有效地将乙醇脱水成乙烯。以竹粉为原料,采用简单的一步分解法合成了生物炭(BC)和磷酸修饰衍生物(HBC)。进一步引入ZSM-5/MOR复合沸石制备HBC-2-ZSM-5/MOR杂化催化剂,可有效防止乙醚的生成,提高乙烯的产量。当微波输入功率为10 W,反应温度为82℃时,乙醇(WHSV = 2 h−1)在HBC-2-ZSM-5/MOR(1.5)催化剂上完全转化,乙烯选择性几乎为100%。在生物乙醇(模型)、中国白酒和啤酒的转化中也得到了类似的结果,表明该策略具有广泛的适用性。潜势机理研究发现,弱酸性、特殊结构和p改性特性能有效抑制乙醚副产物的形成、低聚和焦化过程,有利于促进乙醇选择性转化为乙烯。这项工作通过将微波加热的优势与精确定制的生物炭基催化剂相结合,为低温乙醇转化为乙烯开辟了另一条道路,所有这些都是为了绿色化学的美好未来。
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阿拉丁
sodium hydroxide
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potassium hydroxide
来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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