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This work presents a study on the separation of model compounds representative of mustard husk pyrolysis oil, through a combination of experimental and modelling approaches. Atmospheric and vacuum distillation were used to perform the separation, and the obtained results were validated by means of an Aspen simulation model. To simulate the pyrolysis oil, different fractions present in mustard husk pyrolysis oil were used. Atmospheric distillation was performed at temperatures ranging from 50 to 180 °C, while vacuum distillation was conducted at varying temperatures and pressures. The composition of the distillate and residue was analysed, and it was found that coking occurred due to polymerization reactions, even at moderate temperatures up to ∼100 °C during atmospheric distillation. Therefore, vacuum rotary evaporation was employed to carry out further studies at lower temperatures (50 °C) and pressures (50 mbar), resulting in a recovery percentage of 56 % for lighter fractions and 36 % for heavier fractions, with complete water (62 %) collected in the distillate phase. The simulated feed mixture, which consisted of Guaiacols, furfurals and furan methanols, was distributed equally in both the distillate and residue phases, and the experimental recoveries in distillate and residue phases were found to be similar with simulation values. Further studies are needed to comprehend the separation behaviour of real pyrolysis oil and to minimize polymerization reactions in the column.

Modelling and experimental studies for the recovery of valuable chemical intermediates from mustard husk pyrolysis oil