Mechanochemical Tailoring of Lignin Structure: Influence of Different Particle Sizes in the Organosolv Process

Author:

Bergrath Jonas12ORCID,Zeppetzauer Franz3ORCID,Rumpf Jessica4ORCID,Kamm Birgit35ORCID,Putz Robert3ORCID,Kling Hans‐Willi2,Schulze Margit14ORCID

Affiliation:

1. Department of Natural Sciences Bonn‐Rhein‐Sieg University of Applied Sciences von‐Liebig‐Strasse 20 53359 Rheinbach Germany

2. Department of Chemistry and Biology University of Wuppertal 42119 Wuppertal Germany

3. Kompetenzzentrum Holz GmbH – Competence Center for Wood Chemistry and Wood Composites (Wood K Plus) Altenberger Strasse 69 Linz 4040 Austria

4. Faculty of Agriculture University of Bonn Meckenheimer Allee 174 53115 Bonn Germany

5. Faculty of Environment and Natural Sciences Brandenburg University of Technology Cottbus‐Senftenberg 03046 Cottbus Germany

Abstract

AbstractThe autocatalyzed ethanolic organosolv process is gaining increasing attention for the sulfur‐free isolation of lignin, which is subsequently used as a renewable substitute for various fossil‐based applications. For the first time, the mechanochemical influence of seven different particle sizes of two different biomasses on the respective organosolv lignin structure is examined. Wine pruning (Pinot Noir) and wine pomace (Accent) are used for organosolv process with particle sizes ranging from 2.0–1.6 mm to less than 0.25 mm. As particle size decreases, the weight‐average molecular weight increases, while the total phenol content decreases significantly. Additionally, the distribution of the lignin‐typical monolignols and relevant substructures, as determined by two‐dimensional heteronuclear nuclear magnetic resonance spectra single quantum coherence (HSQC), is observed. The degree of grinding of the biomass has a clear chemical–structural influence on the isolated HG and HGS organosolv lignins. Therefore, it is crucial to understand this influence to apply organosolv lignins in a targeted manner. In the future, particle size specifications in the context of the organosolv process should be expressed in terms of distribution densities rather than in terms of a smaller than specification.

Publisher

Wiley

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