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Issue 11, 2013
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Liquid-phase reforming and hydrodeoxygenation as a two-step route to aromatics from lignin

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Abstract

A two-step approach to the conversion of organosolv, kraft and sugarcane bagasse lignin to monoaromatic compounds of low oxygen content is presented. The first step consists of lignin depolymerization in a liquid phase reforming (LPR) reaction over a 1 wt% Pt/γ-Al2O3 catalyst at 225 °C in alkaline ethanolwater. The first LPR step resulted in a decrease in lignin molecular weight of 32%, 57% and 27% for organosolv, kraft and bagasse lignin, respectively. GC analysis of the depolymerized lignin reaction mixture furthermore showed the formation of alkylated phenol, guaiacol and syringol-type products in 11%, 9% and 5% yields from organosolv, kraft and bagasse lignin, respectively. The lignin-oil that was isolated by extraction of the ethanol–water solution was subjected to a subsequent hydrodeoxygenation (HDO) reaction in the second conversion step. HDO of the lignin-oil was performed in dodecane at 300 °C under 50 bar hydrogen pressure over CoMo/Al2O3 and Mo2C/CNF catalysts. GC analysis of the product mixture obtained after the two-step LPR–HDO process revealed the formation of, amongst others, benzene, toluene, xylenes and ethylmethylbenzenes. Of the total observed monomeric products (9%), 25% consisted of these oxygen-free products. Notably, such products cannot be obtained by direct HDO of lignin. HDO of the lignin-oil at 350 °C resulted in the conversion of all tris-oxygenated products, with 57% of the observed monomeric products now identified as mono-oxygenated phenolics.

Graphical abstract: Liquid-phase reforming and hydrodeoxygenation as a two-step route to aromatics from lignin

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Publication details

The article was received on 14 Jun 2013, accepted on 29 Jul 2013 and first published on 31 Jul 2013


Article type: Paper
DOI: 10.1039/C3GC41150H
Citation: Green Chem., 2013,15, 3049-3056

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    Liquid-phase reforming and hydrodeoxygenation as a two-step route to aromatics from lignin

    A. L. Jongerius, P. C. A. Bruijnincx and B. M. Weckhuysen, Green Chem., 2013, 15, 3049
    DOI: 10.1039/C3GC41150H

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