“…Asphaltene aggregation and self-association (under favorable and unfavorable solubility conditions) have been extensively studied using multiple techniques (optical microscopy, UV-Vis spectroscopy, ultrasmall-, small-and wide-angle scattering, refractive index measurements, quartz crystal resonator (QCR) High Resolution Transmission Electron Microscopy (HRTEM)) [27][28][29][30][31][32][33], indicating that the governing forces driving this phenomenon are primarily of the Van der Waals type, Hydrogen bonding, acid-base interactions and π − π stacking [34][35][36]. The origin of these interactions is the nature of the asphaltene fraction, functionally defined in terms of solubility (soluble in aromatics but insoluble in n-alkanes) and the presence of multiple components (polyaromatic cores, metals, aliphatic chains, heteroatoms and functional groups such as hydroxyl, carbonyl, amine and nitrile, among others) that add to their molecular complexity [37][38][39].…”