CexZn1–xO2 catalysts for conversion of propanoic acid to 3-pentanone via ketonization

IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Navitha Mudoor Vasantha, Basavaraj Kumbarageri, Rawesh Kumar, Ganesh Narayanaswamy, Harsha Murudappa, Sree Karthikayan, Sanjeev P Maradur, Naga Suresh Enjamuri
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Abstract

Ketonization of carboxylic acids offers a highly effective strategy for upgrading bio-oil by reducing its oxygen content and enhancing fuel properties. In this study, a series of CexZn1–xO2 catalysts with varying Ce/Zn ratios were synthesized and evaluated for the ketonization of propanoic acid to produce 3-pentanone, a valuable intermediate with improved thermal stability and hydrophobicity. Among the catalysts tested, Ce0.7Zn0.3O2 catalyst exhibited exceptional performance, achieving >99% conversion of propanoic acid and >99% selectivity toward 3-pentanone at 350 °C, with stable catalytic activity maintained over a period of 3 h. BET surface area analysis revealed that all the catalysts possess mesoporous structures characterized by type-IV isotherms with H3 hysteresis loops. PXRD results indicated the formation of a CeO2-dominated solid solution, with highly dispersed ZnO phase undetectable by diffraction. However, AAS, Raman analysis and FT-IR studies supports the presence of ZnO in the CexZn1–xO2 catalysts. CO2 and NH3-TPD measurements demonstrated that Zn incorporation significantly enhanced the acidic and basic surface sites, which are crucial for propanoic acid ketonization activity. These findings highlight the potential of CexZn1–xO2 catalysts for efficient bio-oil upgrading and contribute to the advancement of renewable fuel technologies through catalytic conversion of low-molecular-weight carboxylic acids.

Graphical abstract

CexZn1–xO2 catalysts with varying Ce/Zn ratios were synthesized and evaluated for the ketonization of propanoic acid to produce 3-pentanone. Among the catalysts tested, Ce0.7Zn0.3O2 catalyst exhibited exceptional performance, achieving >99% propanoic acid and >99% 3-pentanone selectivity at 350 °C, with stable catalytic activity maintained over a period of 3 h.

丙酸酮化制3-戊酮的cezn1 - xo2催化剂
羧酸酮化通过降低生物油的氧含量和提高燃料性能,为生物油的升级提供了一种非常有效的策略。在本研究中,合成了一系列不同Ce/Zn比的cezn1 - xo2催化剂,并对其在丙酸酮化反应中生成3-戊酮进行了评价。在所测试的催化剂中,Ce0.7Zn0.3O2催化剂表现出优异的性能,在350℃下,其丙酸转化率达到99%,对3-戊酮的选择性达到99%,在3 h内保持稳定的催化活性。BET表面积分析表明,所有催化剂都具有具有H3滞后环的ⅳ型等温线的介孔结构。PXRD结果表明,该材料形成了以ceo2为主的固溶体,并伴有高度分散的ZnO相。然而,原子吸收光谱(AAS)、拉曼光谱(Raman)和傅里叶变换红外光谱(FT-IR)研究表明,CexZn1-xO2催化剂中存在ZnO。CO2和NH3-TPD测量结果表明,Zn的加入显著增强了丙酸酮化活性的酸性和碱性表面位点。这些发现突出了cezn1 - xo2催化剂在高效生物油升级方面的潜力,并通过催化低分子量羧酸的转化为可再生燃料技术的进步做出了贡献。摘要合成了不同Ce/Zn比的cezn1 - xo2催化剂,并对其用于丙酸酮化制3-戊酮的反应进行了评价。在所测试的催化剂中,Ce0.7Zn0.3O2催化剂表现出优异的性能,在350℃条件下实现了99%的丙酸和99%的3-戊酮选择性,并在3 h内保持稳定的催化活性。
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来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.10
自引率
5.90%
发文量
107
审稿时长
1 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
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