Heavy crude oils
constitute the largest reserves; however, their
extraction faces several challenges as a result of their high asphaltene
content. Reducing the viscosity by physicochemical treatments or chemical
transformation on heavy asphaltenes is still a challenge because of
matrix complexity. On the other hand, the 1,3-dipolar cycloaddition
(1,3-DC) reaction has been used to increase the solubility and rheological
properties of graphene and fullerenes, suggesting that 1,3-DC on heavy
crude oils can modify directly the chemical structure of titled compounds
affecting their aggregation. Starting from Colombian heavy oils and
purified asphaltenes, we used a set of chemical modifiers based on
long-chain aliphatic and aromatic aldehydes and N-hexylglycine, followed by in situ reactions at
several concentrations. Rheological measurements showed a significant
reduction on crude oil viscosities up to 98% depending upon the alkyl
chain and concentration; furthermore, 1,3-DC reactions between purified
asphaltenes and chemical modifiers were followed by nuclear magnetic
resonance experiments, which give credence to the viscosity reduction
of heavy crude oils based on chemical reactivity.