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

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/gamma-Al2O3 catalyst at 225 degrees C in alkaline ethanol-water. 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 degrees 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 degrees C resulted in the conversion of all tris-oxygenated products, with 57% of the observed monomeric products now identified as mono-oxygenated phenolics.