Francesco Brandi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Francesco Brandi has a total of 41 co-authors. Here are the top co-authors by number of shared publications:
- Majd Al-Naji
Max Planck Institute of Colloids and Interfaces Potsdam Germany
9 shared publications - Bert F. Sels
KU Leuven Celestijnenlaan 200F
5 shared publications - Xian Wu
Center for Sustainable Catalysis and Engineering, KU Leuven, Celestijnenlaan 200f, 3001 Leuven, Belgium
5 shared publications - Bert U. W. Maes
University of Antwerp Groenenborgerlaan 171
4 shared publications - Deepak Raikwar
Center for Sustainable Catalysis and Engineering KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium
4 shared publications - Ewoud Smet
Organic Synthesis Division, Department of Chemistry University of Antwerp Groenenborgerlaan 171 2020 Antwerp Belgium
4 shared publications
Latest Publications
- Open Access
- 25 February 2025
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 27 (17) , 4512-4522
The role of Beta zeolites in the selective single O-demethylation of alkyl-syringols to alkyl-methoxycatechols, a novel polymer building block class
Beta zeolite and water as a solvent enables the single, selective O-demethylation of syringol toward, methoxy catechols, a novel building block family.
- 25 February 2025
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 27 (17) , 4512-4522
Open AccessThe role of Beta zeolites in the selective single O-demethylation of alkyl-syringols to alkyl-methoxycatechols, a novel polymer building block class
Beta zeolite and water as a solvent enables the single, selective O-demethylation of syringol toward, methoxy catechols, a novel building block family.
- Open Access
- 1 November 2024
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 26 (24) , 11832-11859
Advances in catalytic chemical recycling of synthetic textiles
Catalytic chemical depolymerisation is an emerging technology to recycle synthetic textiles and ultimately to enable a circular textile economy. Homogeneous and heterogeneous systems are reviewed.
- 1 November 2024
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 26 (24) , 11832-11859
Open AccessAdvances in catalytic chemical recycling of synthetic textiles
Catalytic chemical depolymerisation is an emerging technology to recycle synthetic textiles and ultimately to enable a circular textile economy. Homogeneous and heterogeneous systems are reviewed.
- 12 February 2024
- Published by Wiley in Angewandte Chemie
- Vol. 136 (10)
Innenrücktitelbild: Advancements and Perspectives toward Lignin Valorization via O‐Demethylation (Angew. Chem. 10/2024)
- 12 February 2024
- Published by Wiley in Angewandte Chemie
- Vol. 136 (10)
Innenrücktitelbild: Advancements and Perspectives toward Lignin Valorization via O‐Demethylation (Angew. Chem. 10/2024)
- 12 February 2024
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 63 (10)
Inside Back Cover: Advancements and Perspectives toward Lignin Valorization via O‐Demethylation (Angew. Chem. Int. Ed. 10/2024)
- 12 February 2024
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 63 (10)
Inside Back Cover: Advancements and Perspectives toward Lignin Valorization via O‐Demethylation (Angew. Chem. Int. Ed. 10/2024)
- 1 February 2024
- Published by Wiley in Angewandte Chemie
- Vol. 136 (10)
Advancements and Perspectives toward Lignin Valorization via O‐Demethylation
Lignin represents the largest aromatic carbon resource in plants, holding significant promise as a renewable feedstock for bioaromatics and other cyclic hydrocarbons in the context of the circular bioeconomy. However, the methoxy groups of aryl methyl ethers, abundantly found in technical lignins and lignin‐derived chemicals, limit their pertinent chemical reactivity and broader applicability. Unlocking the phenolic hydroxyl functionality through O‐demethylation (ODM) has emerged as a valuable approach to mitigate this need and enables further applications. In this review, we provide a comprehensive summary of the progress in the valorization of technical lignin and lignin‐derived chemicals via ODM, both catalytic and non‐catalytic reactions. Furthermore, a detailed analysis of the properties and potential applications of the O‐demethylated products is presented, accompanied by a systematic overview of available ODM reactions. This review primarily focuses on enhancing the phenolic hydroxyl content in lignin‐derived species through ODM, showcasing its potential in the catalytic funneling of lignin and value‐added applications. A comprehensive synopsis and future outlook are included in the concluding section of this review.
- 1 February 2024
- Published by Wiley in Angewandte Chemie
- Vol. 136 (10)
Advancements and Perspectives toward Lignin Valorization via O‐Demethylation
Lignin represents the largest aromatic carbon resource in plants, holding significant promise as a renewable feedstock for bioaromatics and other cyclic hydrocarbons in the context of the circular bioeconomy. However, the methoxy groups of aryl methyl ethers, abundantly found in technical lignins and lignin‐derived chemicals, limit their pertinent chemical reactivity and broader applicability. Unlocking the phenolic hydroxyl functionality through O‐demethylation (ODM) has emerged as a valuable approach to mitigate this need and enables further applications. In this review, we provide a comprehensive summary of the progress in the valorization of technical lignin and lignin‐derived chemicals via ODM, both catalytic and non‐catalytic reactions. Furthermore, a detailed analysis of the properties and potential applications of the O‐demethylated products is presented, accompanied by a systematic overview of available ODM reactions. This review primarily focuses on enhancing the phenolic hydroxyl content in lignin‐derived species through ODM, showcasing its potential in the catalytic funneling of lignin and value‐added applications. A comprehensive synopsis and future outlook are included in the concluding section of this review.
- 1 February 2024
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 63 (10) , e202317257
Advancements and Perspectives toward Lignin Valorization via O‐Demethylation
Lignin represents the largest aromatic carbon resource in plants, holding significant promise as a renewable feedstock for bioaromatics and other cyclic hydrocarbons in the context of the circular bioeconomy. However, the methoxy groups of aryl methyl ethers, abundantly found in technical lignins and lignin‐derived chemicals, limit their pertinent chemical reactivity and broader applicability. Unlocking the phenolic hydroxyl functionality through O‐demethylation (ODM) has emerged as a valuable approach to mitigate this need and enables further applications. In this review, we provide a comprehensive summary of the progress in the valorization of technical lignin and lignin‐derived chemicals via ODM, both catalytic and non‐catalytic reactions. Furthermore, a detailed analysis of the properties and potential applications of the O‐demethylated products is presented, accompanied by a systematic overview of available ODM reactions. This review primarily focuses on enhancing the phenolic hydroxyl content in lignin‐derived species through ODM, showcasing its potential in the catalytic funneling of lignin and value‐added applications. A comprehensive synopsis and future outlook are included in the concluding section of this review.
- 1 February 2024
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 63 (10) , e202317257
Advancements and Perspectives toward Lignin Valorization via O‐Demethylation
Lignin represents the largest aromatic carbon resource in plants, holding significant promise as a renewable feedstock for bioaromatics and other cyclic hydrocarbons in the context of the circular bioeconomy. However, the methoxy groups of aryl methyl ethers, abundantly found in technical lignins and lignin‐derived chemicals, limit their pertinent chemical reactivity and broader applicability. Unlocking the phenolic hydroxyl functionality through O‐demethylation (ODM) has emerged as a valuable approach to mitigate this need and enables further applications. In this review, we provide a comprehensive summary of the progress in the valorization of technical lignin and lignin‐derived chemicals via ODM, both catalytic and non‐catalytic reactions. Furthermore, a detailed analysis of the properties and potential applications of the O‐demethylated products is presented, accompanied by a systematic overview of available ODM reactions. This review primarily focuses on enhancing the phenolic hydroxyl content in lignin‐derived species through ODM, showcasing its potential in the catalytic funneling of lignin and value‐added applications. A comprehensive synopsis and future outlook are included in the concluding section of this review.
- Open Access
- 26 January 2023
- Published by Royal Society of Chemistry (RSC) in RSC Sustainability
- Vol. 1 (3) , 459-469
Flow-through reductive catalytic fractionation of beech wood sawdust
The use of flow-through (FT) systems in the lignin-first approach can improve the proficiency of the process. Herein, the reductive catalytic fractionation of beech wood sawdust was conducted in an FT system using 35Ni/NDC pellets.
- 26 January 2023
- Published by Royal Society of Chemistry (RSC) in RSC Sustainability
- Vol. 1 (3) , 459-469
Open AccessFlow-through reductive catalytic fractionation of beech wood sawdust
The use of flow-through (FT) systems in the lignin-first approach can improve the proficiency of the process. Herein, the reductive catalytic fractionation of beech wood sawdust was conducted in an FT system using 35Ni/NDC pellets.
- Open Access
- 4 February 2022
- Published by Wiley in ChemSusChem
- Vol. 15 (5) , e202102525
Sustainable Sorbitol Dehydration to Isosorbide using Solid Acid Catalysts: Transition from Batch Reactor to Continuous‐Flow System
Isosorbide is one of the most interesting cellulosic‐derived molecules with great potential to be implemented in wide range of products that shaping our daily life. This Review describes the recent developments in the production of isosorbide from sorbitol in batch and continuous‐flow systems under hydrothermal conditions using solid acid catalysts. Moreover, the current hurdles and challenges regarding the synthesis of isosorbide from cellulosic biomass in continuous‐flow process using solid acid catalysts are summarized, as well as the scaling‐up of this process into pilot level, which will lead to an established industrial process with high sustainability metrics.
- 4 February 2022
- Published by Wiley in ChemSusChem
- Vol. 15 (5) , e202102525
Open AccessSustainable Sorbitol Dehydration to Isosorbide using Solid Acid Catalysts: Transition from Batch Reactor to Continuous‐Flow System
Isosorbide is one of the most interesting cellulosic‐derived molecules with great potential to be implemented in wide range of products that shaping our daily life. This Review describes the recent developments in the production of isosorbide from sorbitol in batch and continuous‐flow systems under hydrothermal conditions using solid acid catalysts. Moreover, the current hurdles and challenges regarding the synthesis of isosorbide from cellulosic biomass in continuous‐flow process using solid acid catalysts are summarized, as well as the scaling‐up of this process into pilot level, which will lead to an established industrial process with high sustainability metrics.
- 1 October 2021
- Published by Elsevier in Molecular Catalysis
- Vol. 515
Preparation and functionalization of free-standing nitrogen-doped carbon-based catalyst electrodes for electrocatalytic N2 fixation
- 1 October 2021
- Published by Elsevier in Molecular Catalysis
- Vol. 515
Preparation and functionalization of free-standing nitrogen-doped carbon-based catalyst electrodes for electrocatalytic N2 fixation
- Open Access
- 10 September 2021
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 23 (24) , 9894-9905
Controlled lignosulfonate depolymerization via solvothermal fragmentation coupled with catalytic hydrogenolysis/hydrogenation in a continuous flow reactor
This study presents an efficient and controlled catalytic valorization of a real side product of the agroforestry industry, i.e. , sodium lignosulfonate (LS), in a continuous flow system to either monomers or oligomers.
- 10 September 2021
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 23 (24) , 9894-9905
Open AccessControlled lignosulfonate depolymerization via solvothermal fragmentation coupled with catalytic hydrogenolysis/hydrogenation in a continuous flow reactor
This study presents an efficient and controlled catalytic valorization of a real side product of the agroforestry industry, i.e. , sodium lignosulfonate (LS), in a continuous flow system to either monomers or oligomers.