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溶剂辅助逐步氧化还原法制备负载于沸石NaA上的KO作为丙烯酸乙酯与乙醇迈克尔加成反应的强碱催化剂

Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported KO as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol.

作者信息

Zhang Zhuxiu, Hu Mengnan, Lv Baoshuai, Kang Jingjuan, Tang Jihai, Fei Zhaoyang, Chen Xian, Liu Qing, Cui Mifen, Qiao Xu

机构信息

State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu National Synergetic Innovation Centre for Advanced Materials (SICAM), Nanjing Tech University, No. 5 Xinmofan Road, Nanjing 210009, China.

出版信息

ACS Omega. 2018 Aug 30;3(8):10188-10197. doi: 10.1021/acsomega.8b00704. eCollection 2018 Aug 31.

Abstract

Solid base catalysts featuring green, robustness, and high activity play an important role in the current fine-chemical and petrochemical industry. Normally, the generation of supported KO by thermal decomposition of KNO requires high temperature, and this process can sometimes destroy the structure of supporting materials. We herein report a solvent-assisted stepwise redox (SASR) approach to generate zeolite NaA-supported KO, which we call KO/NaA, that function as the solid base catalyst for Michael addition reaction between ethanol and ethyl acrylate. The solvent-assisted redox decomposition process of KNO at elevated temperature was investigated by thermogravimetry-mass spectrometry. It reveals that after reducing a minor amount of KNO at 400 °C, the organic solvent decomposes to form carbon, which promotes the reduction of KNO to generate strong basicity on the zeolite NaA at 600 °C. The resulting material, KO/NaA-S, exhibits improved catalytic activity in Michael addition reaction over other benchmark base catalysts that have been used in this reaction. This catalyst is durable for at least four catalytic cycles without apparent loss in activity. KO/NaA-S exhibits larger reaction rate constant yet lower activation energy than KO/NaA prepared by thermal decomposition method. The SASR approach described in this paper represents a new blueprint for the generation of the supported alkali oxide as the solid base catalyst.

摘要

具有绿色、稳定性高和高活性的固体碱催化剂在当前精细化工和石油化工行业中发挥着重要作用。通常,通过硝酸钾热分解生成负载型氧化钾需要高温,而此过程有时会破坏载体材料的结构。我们在此报告一种溶剂辅助逐步氧化还原(SASR)方法来生成沸石NaA负载的氧化钾,我们将其称为KO/NaA,它可作为乙醇与丙烯酸乙酯之间迈克尔加成反应的固体碱催化剂。通过热重-质谱联用技术研究了硝酸钾在高温下的溶剂辅助氧化还原分解过程。结果表明,在400℃还原少量硝酸钾后,有机溶剂分解形成碳,这促进了硝酸钾的还原,从而在600℃时在沸石NaA上产生强碱性。所得材料KO/NaA-S在迈克尔加成反应中比该反应中使用的其他基准碱催化剂表现出更高的催化活性。这种催化剂至少可持续四个催化循环而活性无明显损失。与通过热分解法制备的KO/NaA相比,KO/NaA-S表现出更大的反应速率常数和更低的活化能。本文所述的SASR方法为生成作为固体碱催化剂的负载型碱金属氧化物提供了一种新方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db08/6644863/37c444cb4bb5/ao-2018-007044_0011.jpg

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