Support composition engineering of gold catalysts for efficient oxidative esterification of ethylene glycol

• Multi-component oxide supported gold catalyst for oxidative esterification of ethylene glycol to methyl glycolate. • Synergistic modulation of acid-base sites and Au electron density by multi-component support. • Activation energy reduced by ∼70 % via synthesizing the multi-component oxides supported Au. • Under the molecular oxygen mediated, realize high selective conversion of ethylene glycol to methyl glycolate. To address the overcapacity in coal-to-ethylene glycol production, developing eco-friendly process to convert ethylene glycol into high-value-added chemicals is an important topic in current industrial research. In this work, we prepared a multi-component metal oxide-supported Au catalyst through a simple physical mixing and impregnation strategy, and investigated the influence of the support composition on the catalyst activity. Among all tested catalysts, Au/NbZnAlO x exhibited the optimal catalytic performance, achieving a selectivity of 95 % for methyl glycolate, while maintaining good stability (>90 % selectivity) after five cycles. The characterization of XRD, XPS, TPD and ATR-IR indicated that the incorporation of 10 wt% ZnO and 10 wt% Al 2 O 3 into Nb 2 O 5 effectively modulates the balanced distribution of acid-base sites on the catalyst surface and the substrate adsorption capacity. Meanwhile, NbZnAlO x support endowed Au nanoparticles highest electron density, promoting the activation of O 2 , thereby enhancing the catalytic activity. Kinetic studies revealed a remarkable reduction in activation energy from 77 kJ mol -1 to 24 kJ mol -1 upon ZnO/Al 2 O 3 incorporation into Nb 2 O 5 . These findings provide insights into designing multi-component oxide-supported gold catalysts and highlight the critical importance of support composition in optimizing selective oxidation reactions. NbZnAlO x supported Au provides optimal distribution of surface acid-base site and endowed Au nanoparticles highest electron density, promoting moderate substrate adsorption strength and the activation of O 2 , thereby enhancing the catalytic activity.

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Publication Details

Journal
Molecular Catalysis
Published
2025-10-07
DOI
https://doi.org/10.1016/j.mcat.2025.115522
Primary Topic
COVID-19 and healthcare impacts
Type
article
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article

Support composition engineering of gold catalysts for efficient oxidative esterification of ethylene glycol

Molecular Catalysis
COVID-19 and healthcare impacts
article

Support composition engineering of gold catalysts for efficient oxidative esterification of ethylene glycol

article en

Abstract

• Multi-component oxide supported gold catalyst for oxidative esterification of ethylene glycol to methyl glycolate. • Synergistic modulation of acid-base sites and Au electron density by multi-component support. • Activation energy reduced by ∼70 % via synthesizing the multi-component oxides supported Au. • Under the molecular oxygen mediated, realize high selective conversion of ethylene glycol to methyl glycolate. To address the overcapacity in coal-to-ethylene glycol production, developing eco-friendly process to convert ethylene glycol into high-value-added chemicals is an important topic in current industrial research. In this work, we prepared a multi-component metal oxide-supported Au catalyst through a simple physical mixing and impregnation strategy, and investigated the influence of the support composition on the catalyst activity. Among all tested catalysts, Au/NbZnAlO x exhibited the optimal catalytic performance, achieving a selectivity of 95 % for methyl glycolate, while maintaining good stability (>90 % selectivity) after five cycles. The characterization of XRD, XPS, TPD and ATR-IR indicated that the incorporation of 10 wt% ZnO and 10 wt% Al 2 O 3 into Nb 2 O 5 effectively modulates the balanced distribution of acid-base sites on the catalyst surface and the substrate adsorption capacity. Meanwhile, NbZnAlO x support endowed Au nanoparticles highest electron density, promoting the activation of O 2 , thereby enhancing the catalytic activity. Kinetic studies revealed a remarkable reduction in activation energy from 77 kJ mol -1 to 24 kJ mol -1 upon ZnO/Al 2 O 3 incorporation into Nb 2 O 5 . These findings provide insights into designing multi-component oxide-supported gold catalysts and highlight the critical importance of support composition in optimizing selective oxidation reactions. NbZnAlO x supported Au provides optimal distribution of surface acid-base site and endowed Au nanoparticles highest electron density, promoting moderate substrate adsorption strength and the activation of O 2 , thereby enhancing the catalytic activity.

Molecular CatalysisVol. 588
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Dalian National Laboratory for Clean Energy (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 37%
COVID-19 and healthcare impacts
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