Catalytic Lignin Valorization Process for the Production of Aromatic Chemicals and Hydrogen

With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (e...

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Veröffentlicht in:ChemSusChem Jg. 5; H. 8; S. 1602 - 1609
Hauptverfasser: Zakzeski, Joseph, Jongerius, Anna L., Bruijnincx, Pieter C. A., Weckhuysen, Bert M.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Weinheim WILEY-VCH Verlag 01.08.2012
WILEY‐VCH Verlag
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ISSN:1864-5631, 1864-564X, 1864-564X
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Abstract With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (exemplified with kraft, organosolv, and sugarcane bagasse lignin) using a mixture of cheap, bio‐renewable ethanol and water as solvent. Ethanol/water mixtures readily solubilize lignin under moderate temperatures and pressures with little residual solids. The molecular weight of the dissolved lignins was shown to be reduced by gel permeation chromatography and quantitative HSQC NMR methods. The use of liquid‐phase reforming of the solubilized lignin over a Pt/Al2O3 catalyst at 498 K and 58 bar is introduced to yield up to 17 % combined yield of monomeric aromatic oxygenates such as guaiacol and substituted guaiacols generating hydrogen as a useful by‐product. Reduction of the lignin dissolved in ethanol/water using a supported transition metal catalyst at 473 K and 30 bar hydrogen yields up to 6 % of cyclic hydrocarbons and aromatics. A catalytic approach to valorize lignin by using a mixture of cheap, biorenewable ethanol and water as solvent is reported. Liquid‐phase reforming of the solubilized lignin over Pt/Al2O3/co‐catalyst yields monomeric aromatic oxygenates and hydrogen as a useful byproduct. The solvated lignin can also be subjected to a subsequent conversion step, for example, using an appropriate reduction catalyst and hydrogen to yield a different slate of hydrocarbons and aromatics.
AbstractList With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (exemplified with kraft, organosolv, and sugarcane bagasse lignin) using a mixture of cheap, bio‐renewable ethanol and water as solvent. Ethanol/water mixtures readily solubilize lignin under moderate temperatures and pressures with little residual solids. The molecular weight of the dissolved lignins was shown to be reduced by gel permeation chromatography and quantitative HSQC NMR methods. The use of liquid‐phase reforming of the solubilized lignin over a Pt/Al 2 O 3 catalyst at 498 K and 58 bar is introduced to yield up to 17 % combined yield of monomeric aromatic oxygenates such as guaiacol and substituted guaiacols generating hydrogen as a useful by‐product. Reduction of the lignin dissolved in ethanol/water using a supported transition metal catalyst at 473 K and 30 bar hydrogen yields up to 6 % of cyclic hydrocarbons and aromatics.
With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (exemplified with kraft, organosolv, and sugarcane bagasse lignin) using a mixture of cheap, bio‐renewable ethanol and water as solvent. Ethanol/water mixtures readily solubilize lignin under moderate temperatures and pressures with little residual solids. The molecular weight of the dissolved lignins was shown to be reduced by gel permeation chromatography and quantitative HSQC NMR methods. The use of liquid‐phase reforming of the solubilized lignin over a Pt/Al2O3 catalyst at 498 K and 58 bar is introduced to yield up to 17 % combined yield of monomeric aromatic oxygenates such as guaiacol and substituted guaiacols generating hydrogen as a useful by‐product. Reduction of the lignin dissolved in ethanol/water using a supported transition metal catalyst at 473 K and 30 bar hydrogen yields up to 6 % of cyclic hydrocarbons and aromatics. A catalytic approach to valorize lignin by using a mixture of cheap, biorenewable ethanol and water as solvent is reported. Liquid‐phase reforming of the solubilized lignin over Pt/Al2O3/co‐catalyst yields monomeric aromatic oxygenates and hydrogen as a useful byproduct. The solvated lignin can also be subjected to a subsequent conversion step, for example, using an appropriate reduction catalyst and hydrogen to yield a different slate of hydrocarbons and aromatics.
With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (exemplified with kraft, organosolv, and sugarcane bagasse lignin) using a mixture of cheap, bio-renewable ethanol and water as solvent. Ethanol/water mixtures readily solubilize lignin under moderate temperatures and pressures with little residual solids. The molecular weight of the dissolved lignins was shown to be reduced by gel permeation chromatography and quantitative HSQC NMR methods. The use of liquid-phase reforming of the solubilized lignin over a Pt/Al(2)O(3) catalyst at 498 K and 58 bar is introduced to yield up to 17 % combined yield of monomeric aromatic oxygenates such as guaiacol and substituted guaiacols generating hydrogen as a useful by-product. Reduction of the lignin dissolved in ethanol/water using a supported transition metal catalyst at 473 K and 30 bar hydrogen yields up to 6 % of cyclic hydrocarbons and aromatics.With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (exemplified with kraft, organosolv, and sugarcane bagasse lignin) using a mixture of cheap, bio-renewable ethanol and water as solvent. Ethanol/water mixtures readily solubilize lignin under moderate temperatures and pressures with little residual solids. The molecular weight of the dissolved lignins was shown to be reduced by gel permeation chromatography and quantitative HSQC NMR methods. The use of liquid-phase reforming of the solubilized lignin over a Pt/Al(2)O(3) catalyst at 498 K and 58 bar is introduced to yield up to 17 % combined yield of monomeric aromatic oxygenates such as guaiacol and substituted guaiacols generating hydrogen as a useful by-product. Reduction of the lignin dissolved in ethanol/water using a supported transition metal catalyst at 473 K and 30 bar hydrogen yields up to 6 % of cyclic hydrocarbons and aromatics.
Author Weckhuysen, Bert M.
Zakzeski, Joseph
Jongerius, Anna L.
Bruijnincx, Pieter C. A.
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  surname: Zakzeski
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  givenname: Anna L.
  surname: Jongerius
  fullname: Jongerius, Anna L.
  organization: Utrecht University, Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Universiteitsweg 99, 3584 CG Utrecht (The Netherlands), Fax: (+31) 30-251-1027
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  givenname: Pieter C. A.
  surname: Bruijnincx
  fullname: Bruijnincx, Pieter C. A.
  organization: Utrecht University, Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Universiteitsweg 99, 3584 CG Utrecht (The Netherlands), Fax: (+31) 30-251-1027
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  givenname: Bert M.
  surname: Weckhuysen
  fullname: Weckhuysen, Bert M.
  email: b.m.weckhuysen@uu.nl
  organization: Utrecht University, Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Universiteitsweg 99, 3584 CG Utrecht (The Netherlands), Fax: (+31) 30-251-1027
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Snippet With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable...
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SubjectTerms Biomass
biorefinery
Catalysis
Ethanol - chemistry
Hydrocarbons, Aromatic - chemistry
Hydrogen - chemistry
lignin
Lignin - chemistry
liquid phase reforming
phenolics
Pressure
Volatilization
Water - chemistry
Title Catalytic Lignin Valorization Process for the Production of Aromatic Chemicals and Hydrogen
URI https://api.istex.fr/ark:/67375/WNG-X8GWNCHN-H/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcssc.201100699
https://www.ncbi.nlm.nih.gov/pubmed/22740175
https://www.proquest.com/docview/1033451797
Volume 5
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