CO2 hydrogenation to light olefins over Fe–Co/K–Al2O3 catalysts prepared via microwave calcination†

IF 3.1 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Reaction Chemistry & Engineering Pub Date : 2024-10-28 DOI:10.1039/D4RE00428K
Nutkamaithorn Polsomboon, Thanapha Numpilai, Kulpavee Jitapunkul, Kajornsak Faungnawakij, Metta Chareonpanich, Xingda An, Le He, Günther Rupprechter and Thongthai Witoon
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Abstract

This study evaluates the effects of microwave calcination on Fe–Co/K–Al2O3 catalysts for CO2 hydrogenation to light olefins, comparing microwave-treated samples at various power settings (700 W, 616 W, 511 W and 364 W) with a traditionally calcined counterpart. The lowest power setting results in incomplete precursor decomposition, adversely affecting Fe, K, and Al2O3 interactions. At medium power, though decomposition improves, Fe2O3 aggregates due to poor dispersion. Medium-high power produces rod-shaped structures with enhanced Fe and K contact, while the highest setting increases Fe2O3 particle size and Fe–K species content to 35.4%, still below the 37.9% observed in the traditional catalyst. Significantly, the formation of Fe–C species (Fe5C2) correlates positively with Fe–K interactions, enhancing the olefins to paraffins ratio. Additionally, the role of Fe3O4 is vital, providing the highest light olefins yield (24.5%) at an optimal Fe–C/Fe3O4 ratio of 0.34 in the medium-high power sample. Compared to the traditional catalyst, which declines significantly in CO2 conversion and olefin yield due to carbonaceous deposits over time, the medium-high power catalyst shows stable performance and reduced coke formation. Moreover, microwave calcination slashes energy consumption by over 99%, underscoring its potential for more sustainable and efficient catalyst preparation.

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通过微波煅烧制备的 Fe-Co/K-Al2O3 催化剂上的 CO2 加氢制取轻烯烃†。
本研究评估了微波煅烧对Fe-Co / K-Al2O3催化剂CO2加氢制轻质烯烃的影响,比较了不同功率设置(700 W, 616 W, 511 W和364 W)下微波处理的样品与传统煅烧的样品。最低功率设置导致前驱体不完全分解,对Fe、K和Al2O3的相互作用产生不利影响。在中等功率下,虽然分解有所改善,但由于分散性差,Fe2O3聚集。中高功率产生的棒状结构增强了Fe和K的接触,而最高功率使Fe2O3粒度和Fe - K含量增加到35.4%,但仍低于传统催化剂的37.9%。Fe-C组分(Fe5C2)的形成与Fe-K相互作用呈正相关,提高了烯烃与石蜡的比例。此外,Fe3O4的作用是至关重要的,在中高功率样品中,Fe-C /Fe3O4的最佳比为0.34时,可提供最高的光烯烃产率(24.5%)。由于碳质沉积,传统催化剂的CO2转化率和烯烃收率会随着时间的推移而显著下降,而中大功率催化剂表现出稳定的性能,并减少了焦炭的形成。此外,微波煅烧减少了99%以上的能源消耗,强调了它在更可持续和高效的催化剂制备方面的潜力。
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来源期刊
Reaction Chemistry & Engineering
Reaction Chemistry & Engineering Chemistry-Chemistry (miscellaneous)
CiteScore
6.60
自引率
7.70%
发文量
227
期刊介绍: Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society. From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.
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