Heteropolyacids combined with Y zeolite as superior solid acid catalysts to accelerate lactic acid esterification

IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Cui Quan, Yingying Zhou, Hua Chu, Xiaolei Fan, Ningbo Gao
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引用次数: 0

Abstract

BACKGROUND

Ethyl lactate produced via esterification between lactic acid and ethanol can be used in plastics, polymers and food industries and renowned for its biodegradability and low toxicity. However, lactic acid self-catalyzed esterification presents a slow reaction process, and acid catalysts are needed to improve the catalysis. Homogeneous acid catalysts like H2SO4 are corrosive, as well as being difficult to be seperated from the reaction media; therefore, advanced heterogeneous catalysts are more ideal. In this study, two kinds of heteropolyacid–zeolite catalysts, involving loading silicotungstic acid and phosphotungstic acid onto Y zeolite, were synthesized, characterized using X-ray diffraction, NH3 temperature-programmed desorption and scanning electron microscopy and analyzed for their catalytic efficiency in the catalytic esterfication.

RESULTS

Results showed that the Keggin structures of heteropolyacids were retained during the preparation process and strong acid sites of Y zeolite were enriched, which made the main contribution to the esterification of lactic acid and ethanol. Furthermore, the initial-stage reaction rate of esterification was significantly enhanced. During the first hour of esterification, the conversion of lactic acid increased from 18% to 65%. Exp Dec1 index model was employed to determine the activation energies of 60HSiW-Y and 60HPW-Y, which exhibit values of 29.3 and 28.2 kJ mol−1, respectively.

CONCLUSION

This study indicates that Keggin structures of heteropolyacids play a key role in the esterification and heteropolyacid–zeolite catalysts can effectively catalyze the esterification. Meanwhile, the results of the kinetic experiments can be of reference significance for large-scale industrial processes involving esterification. © 2024 Society of Chemical Industry (SCI).

杂多酸与Y型沸石结合作为固体酸催化剂加速乳酸酯化反应
乳酸和乙醇通过酯化反应生产的乳酸乙酯可用于塑料、聚合物和食品工业,并以其可生物降解和低毒而闻名。然而,乳酸自催化酯化反应过程缓慢,需要酸性催化剂来提高催化性能。H2SO4等均相酸性催化剂具有腐蚀性,且难以从反应介质中分离;因此,先进的多相催化剂是比较理想的。本研究合成了两种杂多酸-沸石催化剂,分别在Y型沸石上负载硅钨酸和磷钨酸,采用x射线衍射、NH3程序升温解吸和扫描电镜对其进行了表征,并对其催化酯化的催化效率进行了分析。结果表明,Y型沸石在制备过程中保留了杂多酸的Keggin结构,富集了Y型沸石的强酸位点,对乳酸和乙醇的酯化反应起主要作用。此外,酯化初期反应速率显著提高。在酯化反应的第一个小时,乳酸的转化率从18%提高到65%。采用Exp Dec1指数模型确定60HSiW-Y和60HPW-Y的活化能分别为29.3和28.2 kJ mol−1。结论杂多酸的Keggin结构在酯化反应中起关键作用,杂多酸-沸石催化剂能有效催化酯化反应。同时,动力学实验结果对涉及酯化反应的大规模工业过程具有参考意义。©2024化学工业学会(SCI)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.00
自引率
5.90%
发文量
268
审稿时长
1.7 months
期刊介绍: Journal of Chemical Technology and Biotechnology(JCTB) is an international, inter-disciplinary peer-reviewed journal concerned with the application of scientific discoveries and advancements in chemical and biological technology that aim towards economically and environmentally sustainable industrial processes.
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