Hydrodeoxygenation and hydrocracking of solvolysed lignocellulosic biomass by oxide, reduced and sulphide form of NiMo, Ni, Mo and Pd catalysts

Innovative second-generation biofuel was obtained by a low-temperature ultrasonic liquefaction of waste wood biomass in glycerol, diethylene glycol and p-toluenesulfonic acid, and its hydrotreatment in the presence of various heterogeneous catalysts and hydrogen donor solvents. Depolymerization and solubilization of cellulose, hemicellulose and lignin by using residual glycerin from biodiesel production make solvolysis process highly sustainable thermochemical biomass to liquid (BtL) route. Solvolytic oil containing 25-33 wt% of liquefied spruce and fir sawdust was upgraded by hydrotreatment utilizing heterogeneous catalysis at 300 degrees C and 8 MPa of hydrogen pressure. Prior to kinetic experiments, mass transfer and heat transfer resistances were reduced, and activity of catalytic hydrocracking and hydrodeoxygenation (HDO) was investigated for four NiMo/Al2O3 bifunctional catalysts in oxide, reduced and sulphide form, Ni/Al2O3-SiO2, MoS2, Pd/Al2O3 and Pd/C. Promoting effects of hydrogen donor solvents were investigated for tetralin, phenol, 2-propanol, pyridine, m-cresol, anthracene, cyclohexanol and xylene. Lumped reaction kinetic model was developed to determine kinetics of hydrogenolysis, decarboxylation, decarbonylation and hydrocracking of products of liquefaction, such as levulinic acid, guaiacol and hydroxymethyl furfural (HMF), according to their functional groups and related gaseous products, quantified by Fourier transform infrared spectroscopy. Upgraded liquid product was also characterized for energetic and fuel applications by following its rheological properties and measurements of gross calorific value. (C) 2013 Elsevier B.V. All rights reserved.