Lignin Conversion to Value-Added Small-Molecule Chemicals: Towards Integrated Forest Biorefineries

Research output: ThesisDoctoral Thesis (compilation)

566 Downloads (Pure)


Lignin is the most abundant aromatic biopolymer on Earth and has significant potential as a feedstock for industrial use. Due to its intrinsic heterogeneity and recalcitrance, lignin has been regarded as a low-value side-product in the pulp and paper industry and in second-generation biorefineries. However, novel technologies are currently being explored to utilize lignin as a renewable resource for bio-based chemicals, fuels, and materials. The efficient valorization of lignin would also improve the economics and sustainability of forest-based industries. Deriving value from lignin, beyond low-value heat and power, is thus essential for the success of a global circular bioeconomy employing lignocellulosic biomass as a raw material.
This thesis discusses the possibility of producing high-value chemicals from technical lignin streams via thermochemical–biological methods. The work deals with four major research themes: (1) providing insights into the physicochemical properties of technical lignins that could be valuable in designing routes for their valorization, (2) developing technologies for the thermochemical depolymerization of lignin under batch and continuous-flow conditions, (3) developing strategies for the biological valorization of lignin by combining thermochemical depolymerization with microbial conversion, and (4) assessing the techno-economic viability of lignin as a feedstock for sustainable chemical production in a biorefinery.
Comprehensive physicochemical characterization of technical lignins is crucial in the development of molecularly tailored lignin-based applications. Elucidating the structural and compositional features can facilitate the matching of technical lignin streams with suitable valorization strategies, including thermochemical depolymerization. Two thermochemical depolymerization approaches were investigated for the production of low-molecular-weight aromatics from technical lignin: base-catalyzed depolymerization and oxidative depolymerization. Both approaches were also found to be effective means of pretreatment enabling the microbial conversion of kraft lignin.
Continuous processing allowed hydrothermal lignin treatment at exceptionally short residence times, and this is anticipated to be an important stepping-stone toward technical lignin valorization. Membrane filtration appeared to be a practical method of separating complex depolymerized lignin mixtures for product fractionation and upgrading. Bimetallic catalyst systems based on Cu, Mn, and V improved the oxidative conversion of lignosulfonate and kraft lignins into value-added aromatic compounds. Techno-economic analysis underlined the viability of large-scale chemical production from kraft lignin by oxidative depolymerization, offering opportunities for process integration with traditional pulp mills.
Original languageEnglish
Awarding Institution
  • Department of Chemical Engineering
  • Hulteberg, Christian, Supervisor
  • Turner, Charlotta, Assistant supervisor
  • Wallberg, Ola, Assistant supervisor
Thesis sponsors
Award date2021 Mar 15
Place of PublicationLund, Sweden
ISBN (Print)978-91-7422-782-6
ISBN (electronic) 978-91-7422-783-3
Publication statusPublished - 2021 Feb 19

Bibliographical note

Defence details
Date: 2021-03-15
Time: 09:00
Place: Lecture hall KC:B, Kemicentrum, Naturvetarvägen 14, Faculty of Engineering LTH, Lund University, Lund.
External reviewer(s)
Name: Gosselink, Richard
Title: Dr.
Affiliation: Wageningen Food & Biobased Research, The Netherlands.

Subject classification (UKÄ)

  • Chemical Engineering

Free keywords

  • aromatic monomers
  • biorefinery
  • catalysis
  • kraft lignin
  • lignin depolymerization
  • lignin valorization
  • microbial conversion
  • renewable chemicals
  • techno-economic analysis


Dive into the research topics of 'Lignin Conversion to Value-Added Small-Molecule Chemicals: Towards Integrated Forest Biorefineries'. Together they form a unique fingerprint.

Cite this