2016 AIChE Spring Meeting and 12th Global Congress on Process Safety
(63bg) Molecular Simulation of Controlling Ions and Their Role in Low Salinity IOR for Carbonate Reservoirs
Author
The study of hydrated gas-phase metal ions provides a link between intrinsic chemistry of the isolated ion and its chemistry in solution. The structures and binding enthalpies of a variety of gas-phase and solution mono- and divalent ion hydrates containing up to 12 water molecules have been studied computationally. A DFT and molecular dynamics simulations were employed to study hydrated structures of the form [M(H2O)n]2+.mH2O for calcium and magnesium and [M(H2O)n]+.mH2O for sodium, in which there are n water molecules in the first coordination shell and m water molecules in the second coordination shell. The hydration, dehydration, and interactions of metal ions with Cl-1 and SO-24 have been studied to better understand the mechanism of low salinity IOR. Density functional (DFT) theory using the B3LYP functional, and 6-311++g** basis set has been used. The charge of the metal ion decreases monotonically as the number of water molecules increases in the complex. Extensive calculations of the energetic contribution of individual structural characteristics as well as the energetic trends in binding energy are developed, which will lead to better understanding of how low salinity water IOR works.
Keywords: Hydration, carbonate reservoir, DFT, binding energy, Low Salinity