In
situ combustion (ISC) is one of the highest potential enhanced
oil recovery (EOR) processes for heavy oils. However, several operational
issues, including the formation of highly stable emulsions, have limited
its application. Disclosing the physicochemical proprieties of these
emulsions, especially the chemical nature of the compounds involved
in the stabilization process, has become relevant for the success
of ISC projects. In the present work, the physicochemical changes
at a laboratory-scale low-temperature oxidation (LTO) regimen performed
over a Colombian heavy crude oil were followed by mass spectrometry.
The compositional analyses were performed using both positive-ion
atmospheric pressure photoionization ((+) APPI) and negative-ion electrospray
ionization ((−) ESI) Fourier transform ion cyclotron resonance
mass spectrometry (FT-ICR MS). Further isolation of acidic compounds
and surface-active species allowed us to determine that the process
incorporates a wide variety of compounds to build up the O/W (oil/water)
interface, thus increasing the stabilizing tendency of the emulsions.
During the combustion, oxygen is chemically incorporated to the crude
over hydrocarbon compounds, as well as over sulfur- and nitrogen-containing
compounds, generating classes such as O, O2, O3, O4, OS, NO2, and
NO3 that explain the high viscosity and high stability of the emulsions.