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Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol

[Image: see text] 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 K(2)O by thermal decomposition of KNO(3) requires high temperature, and this process can sometim...

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Autores principales: Zhang, Zhuxiu, Hu, Mengnan, Lv, Baoshuai, Kang, Jingjuan, Tang, Jihai, Fei, Zhaoyang, Chen, Xian, Liu, Qing, Cui, Mifen, Qiao, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644863/
https://www.ncbi.nlm.nih.gov/pubmed/31459147
http://dx.doi.org/10.1021/acsomega.8b00704
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author Zhang, Zhuxiu
Hu, Mengnan
Lv, Baoshuai
Kang, Jingjuan
Tang, Jihai
Fei, Zhaoyang
Chen, Xian
Liu, Qing
Cui, Mifen
Qiao, Xu
author_facet Zhang, Zhuxiu
Hu, Mengnan
Lv, Baoshuai
Kang, Jingjuan
Tang, Jihai
Fei, Zhaoyang
Chen, Xian
Liu, Qing
Cui, Mifen
Qiao, Xu
author_sort Zhang, Zhuxiu
collection PubMed
description [Image: see text] 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 K(2)O by thermal decomposition of KNO(3) 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 K(2)O, which we call K(2)O/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(3) at elevated temperature was investigated by thermogravimetry–mass spectrometry. It reveals that after reducing a minor amount of KNO(3) at 400 °C, the organic solvent decomposes to form carbon, which promotes the reduction of KNO(3) to generate strong basicity on the zeolite NaA at 600 °C. The resulting material, K(2)O/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. K(2)O/NaA-S exhibits larger reaction rate constant yet lower activation energy than K(2)O/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.
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spelling pubmed-66448632019-08-27 Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol Zhang, Zhuxiu Hu, Mengnan Lv, Baoshuai Kang, Jingjuan Tang, Jihai Fei, Zhaoyang Chen, Xian Liu, Qing Cui, Mifen Qiao, Xu ACS Omega [Image: see text] 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 K(2)O by thermal decomposition of KNO(3) 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 K(2)O, which we call K(2)O/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(3) at elevated temperature was investigated by thermogravimetry–mass spectrometry. It reveals that after reducing a minor amount of KNO(3) at 400 °C, the organic solvent decomposes to form carbon, which promotes the reduction of KNO(3) to generate strong basicity on the zeolite NaA at 600 °C. The resulting material, K(2)O/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. K(2)O/NaA-S exhibits larger reaction rate constant yet lower activation energy than K(2)O/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. American Chemical Society 2018-08-30 /pmc/articles/PMC6644863/ /pubmed/31459147 http://dx.doi.org/10.1021/acsomega.8b00704 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Zhang, Zhuxiu
Hu, Mengnan
Lv, Baoshuai
Kang, Jingjuan
Tang, Jihai
Fei, Zhaoyang
Chen, Xian
Liu, Qing
Cui, Mifen
Qiao, Xu
Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol
title Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol
title_full Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol
title_fullStr Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol
title_full_unstemmed Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol
title_short Solvent-Assisted Stepwise Redox Approach To Generate Zeolite NaA-Supported K(2)O as Strong Base Catalyst for Michael Addition of Ethyl Acrylate with Ethanol
title_sort solvent-assisted stepwise redox approach to generate zeolite naa-supported k(2)o as strong base catalyst for michael addition of ethyl acrylate with ethanol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644863/
https://www.ncbi.nlm.nih.gov/pubmed/31459147
http://dx.doi.org/10.1021/acsomega.8b00704
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