Reductive Partial Depolymerization of Acetone Organosolv Lignin to Tailor Lignin Molar Mass, Dispersity, and Reactivity for Polymer Applications

Arjan T. Smit*, Thomas Dezaire, Luke A. Riddell, Pieter C.A. Bruijnincx*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Lignin partial depolymerization by reduction (PDR) was developed as a strategy to tailor a technical lignin’s molar mass and reduce its heterogeneity and to potentially increase the reactivity of lignin hydroxyl groups in polymer applications such as PU foams and coatings. The process aims to cleave remaining lignin β-O-4 linkages, thereby reducing the molar mass of large lignin fragments and overall lignin dispersity. Acetone organosolv lignin from pilot-scale fractionation of industrial-size wood chips was depolymerized using methanol, a Ru/C catalyst, and externally supplied hydrogen. The effect of reaction temperatures (in the presence and absence of the catalyst) was fully detailed using SEC, 31P NMR, and 2D-HSQC NMR analyses of the depolymerized lignin. The Ru/C catalyst promoted molar mass reduction by hydrogenolysis and slightly increased the lignin aliphatic OH content. Process parameter screening showed effective depolymerization at high lignin concentrations but required relatively high catalyst loadings. PDR depolymerization efficiency proved to be dependent on the technical lignin’s quality. A less-condensed lignin with a higher β-O-4 content showed improved ether cleavage, yielding a lower lignin molar mass after PDR and increased formation of 4-n-propanol end groups. Overall, the PDR process provides control over key lignin characteristics, which in turn offers potential to tailor biobased polymer properties for various applications.

Original languageEnglish
Pages (from-to)6070-6080
Number of pages11
JournalACS Sustainable Chemistry and Engineering
Volume11
Issue number15
DOIs
Publication statusPublished - 17 Apr 2023

Bibliographical note

Funding Information:
This project has received TNO funding from the Dutch Ministry of Economic affairs. The authors thank the NMR group at Utrecht University for the access to their facilities. The authors are grateful to the following persons for their excellent contribution to this work: Petra Bonouvrie, Ron van der Laan, Michiel Hoek, Karina Vogelpoel-de Wit, Ben van Egmond, Kasper Tempel, Patrick Kreft, and Dr. André van Zomeren.

Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.

Funding

This project has received TNO funding from the Dutch Ministry of Economic affairs. The authors thank the NMR group at Utrecht University for the access to their facilities. The authors are grateful to the following persons for their excellent contribution to this work: Petra Bonouvrie, Ron van der Laan, Michiel Hoek, Karina Vogelpoel-de Wit, Ben van Egmond, Kasper Tempel, Patrick Kreft, and Dr. André van Zomeren.

Keywords

  • biomass organosolv pretreatment
  • lignocellulose biorefinery
  • reductive depolymerization
  • tailored lignin molar mass and reactivity

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