This is the authors' abstract. We don't add key points for this paper.
Bio-oil obtained via the vacuum pyrolysis of softwood bark residues is a multiphase, viscous, unstable system composed of water-soluble and water-insoluble fractions. Using centrifugation, the bio-oil can be separated into an upper layer (ca. 16 wt %) and a bottom layer (ca. 84 wt %). The upper layer exhibits low contents of water, solid, and ash, as well as a low density, a low acidity, a high content of methanol-insoluble materials, a high viscosity, and a high calorific value. The physicochemical properties of the bottom layer are similar to those of the whole bio-oil, except the bottom layer contains greater contents of ash and water. Microscopic analysis of the bio-oil has revealed a multiphase complex colloidal system that is composed of solid particles, three-dimensional structures, and droplets. The upper layer represents the dispersed droplet phase, which is rich in waxy materials (fatty and resin acids) and water-insoluble compounds. It is the upper layer that, overall, provides the unique colloidal properties to this type of bio-oil. The morphology of the bottom layer is similar to that of the bio-oil matrix. The presence of microstructures in the whole bio-oil has been revealed by differential scanning calorimetry and rheology. The microstructures (e.g., waxy materials) in the bio-oil matrix are, in part, responsible for the bio-oil high viscosity and non-Newtonian behavior that is observed at low temperature (<50 °C). This behavior disappears when the heating temperature reaches the melting point of the three-dimensional structures contained in the bio-oil. The results have confirmed the colloidal nature of the bio-oil investigated.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Ba et al. (2003) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: