Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3

Abstract Acetone is an important solvent and widely used in the synthesis of drugs and polymers. Currently, acetone is mainly generated by the Cumene Process, which employs benzene and propylene as fossil raw materials. Phenol is a co-product of this synthesis. However, this ketone can be generated...

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Main Authors: Clarissa Perdomo Rodrigues, Priscila da Costa Zonetti, Lucia Gorenstin Appel
Format: Article
Language:English
Published: BMC 2017-04-01
Series:Chemistry Central Journal
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13065-017-0249-5
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spelling doaj-fb85bf5c40304881bab61c8add7ba2252021-08-02T10:52:11ZengBMCChemistry Central Journal1752-153X2017-04-0111111110.1186/s13065-017-0249-5Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3Clarissa Perdomo Rodrigues0Priscila da Costa Zonetti1Lucia Gorenstin Appel2Divisão de Catálise e Processos Químicos, Instituto Nacional de TecnologiaDivisão de Catálise e Processos Químicos, Instituto Nacional de TecnologiaDivisão de Catálise e Processos Químicos, Instituto Nacional de TecnologiaAbstract Acetone is an important solvent and widely used in the synthesis of drugs and polymers. Currently, acetone is mainly generated by the Cumene Process, which employs benzene and propylene as fossil raw materials. Phenol is a co-product of this synthesis. However, this ketone can be generated from ethanol (a renewable feedstock) in one-step. The aim of this work is to describe the influence of physical–chemical properties of three different catalysts on each step of this reaction. Furthermore, contribute to improve the description of the mechanism of this synthesis. The acetone synthesis from ethanol was studied employing Cu/ZnO/Al2O3, Ce0.75Zr0.25O2 and ZrO2. It was verified that the acidity of the catalysts needs fine-tuning in order to promote the oxygenate species adsorption and avoid the dehydration of ethanol. The higher the reducibility and the H2O dissociation activity of the catalysts are, the higher the selectivity to acetone is. In relation to the oxides, these properties are associated with the presence of O vacancies. The H2 generation, which occurs during the TPSR, indicates the redox character of this synthesis. The main steps of the acetone synthesis from ethanol are the generation of acetaldehyde, the oxidation of this aldehyde to acetate species (which reduces the catalyst), the H2O dissociation, the oxidation of the catalyst producing H2, and, finally, the ketonization reaction. These pieces of information will support the development of active catalysts for not only the acetone synthesis from ethanol, but also the isobutene and propylene syntheses in which this ketone is an intermediate. Graphical abstract Acetone from ethanol.http://link.springer.com/article/10.1186/s13065-017-0249-5AcetoneEthanolZirconiaCopperCeriaAcetaldehyde
collection DOAJ
language English
format Article
sources DOAJ
author Clarissa Perdomo Rodrigues
Priscila da Costa Zonetti
Lucia Gorenstin Appel
spellingShingle Clarissa Perdomo Rodrigues
Priscila da Costa Zonetti
Lucia Gorenstin Appel
Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3
Chemistry Central Journal
Acetone
Ethanol
Zirconia
Copper
Ceria
Acetaldehyde
author_facet Clarissa Perdomo Rodrigues
Priscila da Costa Zonetti
Lucia Gorenstin Appel
author_sort Clarissa Perdomo Rodrigues
title Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3
title_short Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3
title_full Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3
title_fullStr Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3
title_full_unstemmed Chemicals from ethanol: the acetone synthesis from ethanol employing Ce0.75Zr0.25O2, ZrO2 and Cu/ZnO/Al2O3
title_sort chemicals from ethanol: the acetone synthesis from ethanol employing ce0.75zr0.25o2, zro2 and cu/zno/al2o3
publisher BMC
series Chemistry Central Journal
issn 1752-153X
publishDate 2017-04-01
description Abstract Acetone is an important solvent and widely used in the synthesis of drugs and polymers. Currently, acetone is mainly generated by the Cumene Process, which employs benzene and propylene as fossil raw materials. Phenol is a co-product of this synthesis. However, this ketone can be generated from ethanol (a renewable feedstock) in one-step. The aim of this work is to describe the influence of physical–chemical properties of three different catalysts on each step of this reaction. Furthermore, contribute to improve the description of the mechanism of this synthesis. The acetone synthesis from ethanol was studied employing Cu/ZnO/Al2O3, Ce0.75Zr0.25O2 and ZrO2. It was verified that the acidity of the catalysts needs fine-tuning in order to promote the oxygenate species adsorption and avoid the dehydration of ethanol. The higher the reducibility and the H2O dissociation activity of the catalysts are, the higher the selectivity to acetone is. In relation to the oxides, these properties are associated with the presence of O vacancies. The H2 generation, which occurs during the TPSR, indicates the redox character of this synthesis. The main steps of the acetone synthesis from ethanol are the generation of acetaldehyde, the oxidation of this aldehyde to acetate species (which reduces the catalyst), the H2O dissociation, the oxidation of the catalyst producing H2, and, finally, the ketonization reaction. These pieces of information will support the development of active catalysts for not only the acetone synthesis from ethanol, but also the isobutene and propylene syntheses in which this ketone is an intermediate. Graphical abstract Acetone from ethanol.
topic Acetone
Ethanol
Zirconia
Copper
Ceria
Acetaldehyde
url http://link.springer.com/article/10.1186/s13065-017-0249-5
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