MgO-based catalysts for selective delignification of lignocellulosic waste and carboxylic acids production under mild hydrothermal conditions

Lignocellulosic biomass offers a sustainable alternative to traditional raw materials. However, its complex structure, and particularly the presence of lignin, presents a significant challenge for its conversion into valuable products. This study explores the catalytic performance of magnesium oxide (MgO) based materials for the selective delignification of lignocellulosic waste and concomitant carboxylic acids production. Different MgO samples have been synthesized through various synthetical methods with the purpose of promoting the selective delignification of a lignocellulose waste while minimizing the degradation of other polymers (cellulose and hemicellulose). The resultant lignin-free holocellulose solid after selective depolymerization might be used in subsequent fermentation processes. The catalytic results demonstrated that MgO synthesized by a sol-gel method exhibited the highest catalytic activity, achieving ca. 90 % lignin conversion with minimal degradation of cellulose and hemicellulose and outstanding production of carboxylic acids (ca. 30 % of the carbon of the degraded polymers was converted into carboxylic acids). The high concentration of medium-strength base sites combined with significant macroporosity are crucial for enhancing the catalytic performance of MgO-based catalysts. Importantly, these results were achieved under mild conditions (120 °C) using water as a solvent and without addition of external oxidant agents. Furthermore, the study observed a significant production of valuable (di)carboxylic acids, such as fumaric acid during the depolymerization process over optimized MgO catalyst. This research provides valuable insights into the potential of MgO as a sustainable catalyst for the selective conversion of lignin present in lignocellulosic biomass into valuable chemicals and biofuels. • MgO synthesis affects selective delignification of lignocellulosic waste and carboxylic acid production. • Sol-gel synthesized MgO exhibits high macroporosity, moderate basicity and cubic structure. • Open crystalline MgO structure with mild basicity promotes selective delignification and production of carboxylic acids. • Valuable di-carboxylic acids are formed by means of selective delignification over MgO catalyst.

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Publication Details

Journal
Biomass and Bioenergy
Published
2025-05-01
DOI
https://doi.org/10.1016/j.biombioe.2025.107936
Citations
3
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
2.02

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article

MgO-based catalysts for selective delignification of lignocellulosic waste and carboxylic acids production under mild hydrothermal conditions

María Orfila, Nora Vidal, Fernando Martı́nez, María Ventura et al.
3 citations
Biomass and Bioenergy
Catalysis for Biomass Conversion
2.02
article

MgO-based catalysts for selective delignification of lignocellulosic waste and carboxylic acids production under mild hydrothermal conditions

María Orfila, Nora Vidal, Fernando Martı́nez, María Ventura, Juan A. Melero
article en
3 citations

Abstract

Lignocellulosic biomass offers a sustainable alternative to traditional raw materials. However, its complex structure, and particularly the presence of lignin, presents a significant challenge for its conversion into valuable products. This study explores the catalytic performance of magnesium oxide (MgO) based materials for the selective delignification of lignocellulosic waste and concomitant carboxylic acids production. Different MgO samples have been synthesized through various synthetical methods with the purpose of promoting the selective delignification of a lignocellulose waste while minimizing the degradation of other polymers (cellulose and hemicellulose). The resultant lignin-free holocellulose solid after selective depolymerization might be used in subsequent fermentation processes. The catalytic results demonstrated that MgO synthesized by a sol-gel method exhibited the highest catalytic activity, achieving ca. 90 % lignin conversion with minimal degradation of cellulose and hemicellulose and outstanding production of carboxylic acids (ca. 30 % of the carbon of the degraded polymers was converted into carboxylic acids). The high concentration of medium-strength base sites combined with significant macroporosity are crucial for enhancing the catalytic performance of MgO-based catalysts. Importantly, these results were achieved under mild conditions (120 °C) using water as a solvent and without addition of external oxidant agents. Furthermore, the study observed a significant production of valuable (di)carboxylic acids, such as fumaric acid during the depolymerization process over optimized MgO catalyst. This research provides valuable insights into the potential of MgO as a sustainable catalyst for the selective conversion of lignin present in lignocellulosic biomass into valuable chemicals and biofuels. • MgO synthesis affects selective delignification of lignocellulosic waste and carboxylic acid production. • Sol-gel synthesized MgO exhibits high macroporosity, moderate basicity and cubic structure. • Open crystalline MgO structure with mild basicity promotes selective delignification and production of carboxylic acids. • Valuable di-carboxylic acids are formed by means of selective delignification over MgO catalyst.

Biomass and BioenergyVol. 199
Universidad Rey Juan Carlos (ES)
Agencia Estatal de Investigación
Openalex Percentile: Top 14%
Catalysis for Biomass Conversion
2.02
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