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
Abstract
High Resolution Image Download MS PowerPoint Slide 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, 31 P 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.