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微波处理的水滑石类化合物在丙酮自缩合反应中的催化活性研究

Study of the Catalytic Activity of the Compounds Hydrotalcite Type Treated by Microwave in the Self-Condensation of Acetone.

作者信息

Houssaini Jamal, Naciri Bennani Mohammed, Ziyat Hamid, Arhzaf Said, Qabaqous O, Amhoud Abdellatid

机构信息

LCBAE, Laboratory of Chemistry and Biology Applied to the Environment, MAC, Research Team "Materials and Applied Catalysis", Chemistry Department, Moulay Ismail University, B.P. 11201 Zitoune, Meknes 50000, Morocco.

出版信息

Int J Anal Chem. 2021 Dec 23;2021:1551586. doi: 10.1155/2021/1551586. eCollection 2021.

DOI:10.1155/2021/1551586
PMID:34976065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8718331/
Abstract

The self-condensation reaction of acetone, producing diacetone alcohol (DAA), is of great industrial importance. It was used to study the catalytic activity of Mg-Al catalysts synthesized by the coprecipitation method. For this purpose, we synthesized Mg-Al based hydrotalcite with a molar ratio of 3, obtained either after conventional heating or after microwave irradiation with of 100 W for three minutes. Structural and chemical properties of the obtained catalysts were characterized, using different techniques: X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), scanning electron microscope (SEM), equipped with energy dispersive X-ray (EDX), and specific surface area of the catalysts were determined by the methylene blue (MB) adsorption method. Also, these catalysts were tested in the self-condensation reaction of acetone at 273 K in the liquid phase without solvent, a reaction which requires very high catalytic activity. The microwave treatment improves the catalyst activity, and the conversion of acetone to diacetone alcohol increases from 13.2 to 18.3% after 8 h of reaction. Moreover, the microwave-treated hydrotalcite catalyst, calcined at 723 K and rehydrated under a flow of N, is the most active and gives conversion of acetone of 52% under the same reaction conditions.

摘要

丙酮的自缩合反应生成二丙酮醇(DAA),具有重要的工业意义。该反应被用于研究通过共沉淀法合成的镁铝催化剂的催化活性。为此,我们合成了镁铝摩尔比为3的水滑石,分别通过常规加热或100瓦微波辐射三分钟后获得。使用不同技术对所得催化剂的结构和化学性质进行了表征:X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、配备能量色散X射线(EDX)的扫描电子显微镜(SEM),并通过亚甲基蓝(MB)吸附法测定催化剂的比表面积。此外,在无溶剂的液相中于273K下对这些催化剂进行丙酮自缩合反应测试,该反应需要非常高的催化活性。微波处理提高了催化剂活性,反应8小时后丙酮转化为二丙酮醇的转化率从13.2%提高到18.3%。此外,在723K下煅烧并在氮气流中再水化的微波处理水滑石催化剂活性最高,在相同反应条件下丙酮转化率为52%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/99de68f5851a/IJAC2021-1551586.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/1ba293d97e0a/IJAC2021-1551586.sch.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/08c98812836b/IJAC2021-1551586.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/643536f6eb8a/IJAC2021-1551586.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/36e096b43e76/IJAC2021-1551586.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/0f370e80a5ed/IJAC2021-1551586.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/fa1a8289009d/IJAC2021-1551586.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/99de68f5851a/IJAC2021-1551586.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/1ba293d97e0a/IJAC2021-1551586.sch.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/08c98812836b/IJAC2021-1551586.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/643536f6eb8a/IJAC2021-1551586.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/36e096b43e76/IJAC2021-1551586.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/0f370e80a5ed/IJAC2021-1551586.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/fa1a8289009d/IJAC2021-1551586.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1897/8718331/99de68f5851a/IJAC2021-1551586.006.jpg

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本文引用的文献

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Chem Rev. 2012 Jul 11;112(7):4124-55. doi: 10.1021/cr200434v. Epub 2012 Mar 27.
2
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Chemistry. 2005 Jan 7;11(2):728-39. doi: 10.1002/chem.200400409.