Journal
ENERGY & FUELS
Volume 24, Issue 1, Pages 683-689Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ef900845t
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Funding
- Chevron Technology Ventures
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Milled wood lignin samples from Untreated Loblolly pine, post-ethanol organosolv pretreatment, and ethanol organosolv dissolved lignin were isolated and characterized by quantitative C-13 and P-31 nuclear Magnetic resonance (NMR) spectroscopy. beta-O-4 linkages are the predominant substructures Present ill lignin from the starting material, its well as after the pretreatment. During organosolv treatment of Loblolly pine, acid-catalyzed cleavage of beta-O-4 linkages and ester bonds were the major mechanisms of lignin cleavage. This degradative pathway results ill the formation of a dissolved ethanol organosolv lignin, which is more condensed and has a lower molecular weight than the starting lignin. The residual lignin isolated from the solid pretreated residue was also more condensed. Results front quantitative C-13 and P-31 NMR show that the residual and dissolved lignin fractions after pretreatment have it higher abundance of phenols and carboxylic acids and lower aliphatic carbon content and may be suitable as antioxidants or other value-added lignin products.
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