Heterogeneous Catalytic Hydrogenation of Biobased Levulinic and Succinic Acids in Aqueous Solutions

Supported noble‐metal catalysts (Ru, Pd or Pt) and the corresponding Re‐promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reactio...

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Published in:ChemSusChem Vol. 6; no. 12; pp. 2388 - 2395
Main Authors: Corbel-Demailly, Louis, Ly, Bao-Khanh, Minh, Doan-Pham, Tapin, Benoit, Especel, Catherine, Epron, Florence, Cabiac, Amandine, Guillon, Emmanuelle, Besson, Michèle, Pinel, Catherine
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 01-12-2013
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Abstract Supported noble‐metal catalysts (Ru, Pd or Pt) and the corresponding Re‐promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reaction conditions. The highest selectivity to 1,4‐pentanediol of 82 % is achieved at 140 °C in the presence of the 1.9 % Ru–3.6 % Re/C catalyst. Switching between diols and lactones: This article focuses mainly on the comparison of the reactivity of two biobased carboxylic acids, namely levulinic acid and succinic acid, in water in the presence of carbon‐supported noble metals. The optimization of the reaction conditions allows to increase the yield and selectivity to diols (butanediol and pentanediol). Thus, it is possible to obtain pentanediol from levulinic acid under milder conditions compared to succinic acid.
AbstractList Supported noble-metal catalysts (Ru, Pd or Pt) and the corresponding Re-promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reaction conditions. The highest selectivity to 1,4-pentanediol of 82 % is achieved at 140 °C in the presence of the 1.9 % Ru-3.6 % Re/C catalyst.
Supported noble-metal catalysts (Ru, Pd or Pt) and the corresponding Re-promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reaction conditions. The highest selectivity to 1,4-pentanediol of 82% is achieved at 140 degrees C in the presence of the 1.9%Ru-3.6%Re/C catalyst.
Supported noble‐metal catalysts (Ru, Pd or Pt) and the corresponding Re‐promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reaction conditions. The highest selectivity to 1,4‐pentanediol of 82 % is achieved at 140 °C in the presence of the 1.9 % Ru–3.6 % Re/C catalyst. Switching between diols and lactones: This article focuses mainly on the comparison of the reactivity of two biobased carboxylic acids, namely levulinic acid and succinic acid, in water in the presence of carbon‐supported noble metals. The optimization of the reaction conditions allows to increase the yield and selectivity to diols (butanediol and pentanediol). Thus, it is possible to obtain pentanediol from levulinic acid under milder conditions compared to succinic acid.
Abstract Supported noble‐metal catalysts (Ru, Pd or Pt) and the corresponding Re‐promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reaction conditions. The highest selectivity to 1,4‐pentanediol of 82 % is achieved at 140 °C in the presence of the 1.9 % Ru–3.6 % Re/C catalyst.
Supported noble-metal catalysts (Ru, Pd or Pt) and the corresponding Re-promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic acids. Levulinic acid and succinic acid are converted into the lactones or the diols depending on the nature of the catalyst and the reaction conditions. The highest selectivity to 1,4-pentanediol of 82% is achieved at 140°C in the presence of the 1.9%Ru-3.6%Re/C catalyst. [PUBLICATION ABSTRACT]
Author Minh, Doan-Pham
Especel, Catherine
Besson, Michèle
Corbel-Demailly, Louis
Tapin, Benoit
Cabiac, Amandine
Pinel, Catherine
Guillon, Emmanuelle
Epron, Florence
Ly, Bao-Khanh
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  surname: Corbel-Demailly
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  organization: IRCELYON, Institut de recherches sur la catalyse et l'environnement de Lyon, UMR 5256 CNRS-Université Lyon1, 2 Avenue Albert Einstein, 69626 Villeurbanne (France)
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  surname: Ly
  fullname: Ly, Bao-Khanh
  organization: IRCELYON, Institut de recherches sur la catalyse et l'environnement de Lyon, UMR 5256 CNRS-Université Lyon1, 2 Avenue Albert Einstein, 69626 Villeurbanne (France)
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  givenname: Doan-Pham
  surname: Minh
  fullname: Minh, Doan-Pham
  organization: IRCELYON, Institut de recherches sur la catalyse et l'environnement de Lyon, UMR 5256 CNRS-Université Lyon1, 2 Avenue Albert Einstein, 69626 Villeurbanne (France)
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  givenname: Benoit
  surname: Tapin
  fullname: Tapin, Benoit
  organization: IC2MP, Institut de Chimie des Milieux et Matériaux de Poitiers, UMR 7285 CNRS-Université de Poitiers, 4 rue Michel Brunet, 86022 Poitiers (France)
– sequence: 5
  givenname: Catherine
  surname: Especel
  fullname: Especel, Catherine
  organization: IC2MP, Institut de Chimie des Milieux et Matériaux de Poitiers, UMR 7285 CNRS-Université de Poitiers, 4 rue Michel Brunet, 86022 Poitiers (France)
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  givenname: Florence
  surname: Epron
  fullname: Epron, Florence
  organization: IC2MP, Institut de Chimie des Milieux et Matériaux de Poitiers, UMR 7285 CNRS-Université de Poitiers, 4 rue Michel Brunet, 86022 Poitiers (France)
– sequence: 7
  givenname: Amandine
  surname: Cabiac
  fullname: Cabiac, Amandine
  organization: IFPEN-Lyon, BP3, 69360 Solaize (France)
– sequence: 8
  givenname: Emmanuelle
  surname: Guillon
  fullname: Guillon, Emmanuelle
  organization: IFPEN-Lyon, BP3, 69360 Solaize (France)
– sequence: 9
  givenname: Michèle
  surname: Besson
  fullname: Besson, Michèle
  organization: IRCELYON, Institut de recherches sur la catalyse et l'environnement de Lyon, UMR 5256 CNRS-Université Lyon1, 2 Avenue Albert Einstein, 69626 Villeurbanne (France)
– sequence: 10
  givenname: Catherine
  surname: Pinel
  fullname: Pinel, Catherine
  email: catherine.pinel@ircelyon.univ-lyon1.fr
  organization: IRCELYON, Institut de recherches sur la catalyse et l'environnement de Lyon, UMR 5256 CNRS-Université Lyon1, 2 Avenue Albert Einstein, 69626 Villeurbanne (France)
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Issue 12
Keywords biomass
diols
heterogeneous catalysis
hydrogenation
carboxylic acids
Language English
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Snippet Supported noble‐metal catalysts (Ru, Pd or Pt) and the corresponding Re‐promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic...
Supported noble-metal catalysts (Ru, Pd or Pt) and the corresponding Re-promoted catalysts exhibit a high activity for the hydrogenation of biobased carboxylic...
Abstract Supported noble‐metal catalysts (Ru, Pd or Pt) and the corresponding Re‐promoted catalysts exhibit a high activity for the hydrogenation of biobased...
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SubjectTerms biomass
Carbon - chemistry
carboxylic acids
Catalysis
Chemical Sciences
diols
Environment and Society
Environmental Sciences
heterogeneous catalysis
Hydrogenation
Levulinic Acids - chemistry
Metals, Heavy - chemistry
Solutions
Succinates - chemistry
Title Heterogeneous Catalytic Hydrogenation of Biobased Levulinic and Succinic Acids in Aqueous Solutions
URI https://api.istex.fr/ark:/67375/WNG-4037CWHW-W/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcssc.201300608
https://www.ncbi.nlm.nih.gov/pubmed/24039162
https://www.proquest.com/docview/1466171996
https://search.proquest.com/docview/1467063218
https://hal.science/hal-00941355
Volume 6
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