Full Paper
Fractionation of Organosolv Lignin from Olive Tree Clippings and its Valorization to Simple Phenolic Compounds
Article first published online: 12 FEB 2013
DOI: 10.1002/cssc.201200755
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Toledano, A., Serrano, L., Balu, A. M., Luque, R., Pineda, A. and Labidi, J. (2013), Fractionation of Organosolv Lignin from Olive Tree Clippings and its Valorization to Simple Phenolic Compounds. ChemSusChem, 6: 529–536. doi: 10.1002/cssc.201200755
Publication History
- Issue published online: 4 MAR 2013
- Article first published online: 12 FEB 2013
- Manuscript Revised: 27 NOV 2012
- Manuscript Received: 9 OCT 2012
Funded by
- Spanish Ministry of Science and Innovation. Grant Number: CTQ2010-19844-C02-02
- Juan de la Cierva contract. Grant Number: JCI-2011-09399
- Spanish MICINN. Grant Numbers: RYC-2009-04199, P10-FQM-6711
- Junta de Andalucia. Grant Number: CTQ2011 28954-C02-02
Keywords:
- biomass;
- depolymerization;
- hydrogenolysis;
- heterogeneous catalysis;
- ultrafiltration
Abstract
Lignin valorization practices have attracted a great deal of interest in recent years due to the large excess of lignin produced by the pulp and paper industry, together with second-generation bioethanol plants. In this work, a new lignin valorization approach is proposed. It involves ultrafiltration as a fractionation process to separate different molecular weight lignin fractions followed by a hydrogen-free, mild, hydrogenolytic, heterogeneously catalyzed methodology assisted by microwave irradiation to obtain simple phenolic, monomeric products by depolymerization using a nickel-based catalyst. The main products obtained were desaspidinol, syringaldehyde, and syringol; this proves the efficiency of the depolymerization conditions applied. The concentration of these observed compounds increased when the molecular weights of the lignin fractions increased. The applied depolymerization conditions, which take advantage of the use of formic acid as a hydrogen-donating solvent, did not generate any biochar in the systems.

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