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This work investigates the correlation of the reaction conditions and the reaction medium composition with the deactivation behavior of a Ni/La2O3-αAl2O3 catalyst used in the steam reforming of bio-oil.

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This work analyses the composition, morphology, and thermal behavior of the carbonaceous materials deposited during the thermal treatment of bio-oil (thermal pyrolytic lignin-TPL). The bio-oil was obtained by flash pyrolysis of lignocellulosic biomass (pine sawdust), and the TPLs were obtained in the 400-700 °C range. The TPLs were characterized by performing elemental analysis; (13)C NMR, Raman, FTIR, and X-ray photoelectron spectroscopy; SEM; and temperature-programmed oxidation analyzed by differential thermogravimetry and differential scanning calorimetry. The results are compared to a commercial lignin (CL). The TPLs have lower oxygen and hydrogen contents and a greater aromaticity and structural order than the CL material. Based on these features, different valorization routes are proposed: the TPL obtained at 500 °C is suitable for use as a fuel, and the TPL obtained at 700 °C has a suitable morphology and composition for use as an adsorbent or catalyst support.

The characterization of coke deposited on a Ni/La2O3‐αAl2O3 catalyst used in the steam reforming of bio‐oil has been studied by temperature programmed oxidation (TPO) coupled with different in situ techniques: thermogravimetry (TG), modulated thermogravimetry (MTG), FTIR spectroscopy with mass spectrometry (MS), Raman spectroscopy, and differential scanning calorimetry (DSC). The steam reforming of bio‐oil was carried out in a reactor equipment with two steps in series, comprising bio‐oil thermal treatment (500 °C) and subsequent reforming in a fluidized bed reactor (550–700 °C; and steam‐to‐carbon ratio, 1.5–6). TG/MS‐TPO experiments identify encapsulating and filamentous coke, and a more detailed analysis using other in situ techniques enable to characterize the nature and location of 4 types of coke: (i) an encapsulating coke with aliphatic nature placed in the most superficial layers; (ii) an encapsulating coke with higher aromatic nature in inner layers; (iii) the most superficial layers of a filamentous coke, further from active sites and with a more carbonized structure compared to encapsulating coke; and (iv) an innermost and mainly polyaromatic filamentous coke with a low oxygenates content.

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