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Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles

[Image: see text] Gold nanoparticles (Au NPs) supported on a nanostructured gamma alumina (γ-Al(2)O(3)) fiber can exhibit excellent catalytic activity for the conversion of 5-hydroxymethylfurfural to produce its ester derivative, dimethyl 2,5-furandicarboxylate (FDMC). γ-Al(2)O(3) was synthesized us...

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Autores principales: Weerathunga, Helapiyumi, Sarina, Sarina, Zhu, Huai-Yong, Waclawik, Eric R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905805/
https://www.ncbi.nlm.nih.gov/pubmed/33644581
http://dx.doi.org/10.1021/acsomega.0c05541
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author Weerathunga, Helapiyumi
Sarina, Sarina
Zhu, Huai-Yong
Waclawik, Eric R.
author_facet Weerathunga, Helapiyumi
Sarina, Sarina
Zhu, Huai-Yong
Waclawik, Eric R.
author_sort Weerathunga, Helapiyumi
collection PubMed
description [Image: see text] Gold nanoparticles (Au NPs) supported on a nanostructured gamma alumina (γ-Al(2)O(3)) fiber can exhibit excellent catalytic activity for the conversion of 5-hydroxymethylfurfural to produce its ester derivative, dimethyl 2,5-furandicarboxylate (FDMC). γ-Al(2)O(3) was synthesized using a PEG surfactant to generate oxide fibers that randomly stack together into irregular shapes. The average particle sizes of the Au NPs are 1–6 nm, where the catalytically active Au (111) surface is the exposed facet. This 3D nanocatalyst architecture enhances the 5-hydroxymethylfurfural (HMF) oxidative esterification because HMF reactant molecules can readily diffuse into this fibrous structure and adsorb to active catalytic sites, while ester product molecules can diffuse out. Up to 99% HMF conversion and 90% FDMC selectivity can be obtained at a low reaction temperature of 45 °C, and the catalyst shows excellent recyclability. Increasing the Au content in the catalyst minimizes the requirement of a base for HMF conversion. Thus, the Au NPs supported on γ-Al(2)O(3) can drive HMF esterification to FDMC efficiently with high product selectivity under very mild reaction conditions, omitting the need for an additional esterification step of the HMF acid.
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spelling pubmed-79058052021-02-26 Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles Weerathunga, Helapiyumi Sarina, Sarina Zhu, Huai-Yong Waclawik, Eric R. ACS Omega [Image: see text] Gold nanoparticles (Au NPs) supported on a nanostructured gamma alumina (γ-Al(2)O(3)) fiber can exhibit excellent catalytic activity for the conversion of 5-hydroxymethylfurfural to produce its ester derivative, dimethyl 2,5-furandicarboxylate (FDMC). γ-Al(2)O(3) was synthesized using a PEG surfactant to generate oxide fibers that randomly stack together into irregular shapes. The average particle sizes of the Au NPs are 1–6 nm, where the catalytically active Au (111) surface is the exposed facet. This 3D nanocatalyst architecture enhances the 5-hydroxymethylfurfural (HMF) oxidative esterification because HMF reactant molecules can readily diffuse into this fibrous structure and adsorb to active catalytic sites, while ester product molecules can diffuse out. Up to 99% HMF conversion and 90% FDMC selectivity can be obtained at a low reaction temperature of 45 °C, and the catalyst shows excellent recyclability. Increasing the Au content in the catalyst minimizes the requirement of a base for HMF conversion. Thus, the Au NPs supported on γ-Al(2)O(3) can drive HMF esterification to FDMC efficiently with high product selectivity under very mild reaction conditions, omitting the need for an additional esterification step of the HMF acid. American Chemical Society 2021-02-10 /pmc/articles/PMC7905805/ /pubmed/33644581 http://dx.doi.org/10.1021/acsomega.0c05541 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Weerathunga, Helapiyumi
Sarina, Sarina
Zhu, Huai-Yong
Waclawik, Eric R.
Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles
title Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles
title_full Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles
title_fullStr Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles
title_full_unstemmed Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles
title_short Oxidative Esterification of 5-Hydroxymethylfurfural into Dimethyl 2,5-Furandicarboxylate Using Gamma Alumina-Supported Gold Nanoparticles
title_sort oxidative esterification of 5-hydroxymethylfurfural into dimethyl 2,5-furandicarboxylate using gamma alumina-supported gold nanoparticles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905805/
https://www.ncbi.nlm.nih.gov/pubmed/33644581
http://dx.doi.org/10.1021/acsomega.0c05541
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