Cookies

We use cookies to ensure that we give you the best experience on our website. By continuing to browse this repository, you give consent for essential cookies to be used. You can read more about our Privacy and Cookie Policy.


Durham Research Online
You are in:

Atomistic Insight into the Behavior of Ions at an Oil-Bearing Hydrated Calcite Surface: Implication to Ion-Engineered Waterflooding

Badizad, Mohammad Hasan and Koleini, Mohammad Mehdi and Greenwell, Hugh Christopher and Ayatollahi, Shahab and Ghazanfari, Mohammad Hossein (2021) 'Atomistic Insight into the Behavior of Ions at an Oil-Bearing Hydrated Calcite Surface: Implication to Ion-Engineered Waterflooding.', Energy & fuels., 35 (16). pp. 13039-13054.

Abstract

This research provides an atomistic picture of the role of ions in modulating the microstructural features of an oil-contaminated calcite surface. This is of crucial importance for the rational design of ion-engineered waterflooding, a promising technique for enhancing oil recovery from carbonate reservoirs. Inspired by a conventional lab-scale procedure, an integrated series of molecular dynamics (MD) simulations were carried out to resolve the relative contribution of the major ionic constituent of natural brines (i.e., Na+, Cl–, Mg2+, Ca2+, and SO42–) when soaking an oil-bearing calcite surface in different electrolyte solutions of same salinity, namely, CaCl2, MgCl2, Na2SO4, MgSO4, and deionized water (DW). In all cases, we observed the gradual detachment of polar oil molecules (mimicked by decanoate) already paired to Na+ cations, covering the calcite substrate in such a way that carboxylate groups were in contact with the treating solution. The appearance of such a negatively charged interface in conjunction with the bare calcite/brine surface is a likely nanometric source for the disparity of surface characteristics of oil-bearing rocks reported in the literature. The MD results showed the affinity of divalent cations (Ca2+ or Mg2+) for pairing with negatively charged carboxylate functional groups, thereby facilitating desorption of decanoates. Having a compact solvation shell, Mg2+ was not as effective as Ca2+ cations; however, its performance was enhanced in the presence of sulfate anions. We further figured out the tendency of SO42– anions to shielding Na+ sites over the calcite surface, thus limiting the chance of readsorption of carboxylate compounds. Consistent with lab experiences, sulfate was found to assist the access of magnesium cations to the calcite surface as well. Altogether, the present results provide us with a molecular-level validation for the well-known multicomponent ion exchange mechanism proposed for the wettability alteration of carbonate rocks through enriching the divalent ionic content of the injection brine solution.

Item Type:Article
Full text:Publisher-imposed embargo until 09 August 2022.
(AM) Accepted Manuscript
File format - PDF
(2785Kb)
Status:Peer-reviewed
Publisher Web site:https://doi.org/10.1021/acs.energyfuels.1c01357
Publisher statement:This document is the Accepted Manuscript version of a Published Work that appeared in final form in Energy & Fuels, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.energyfuels.1c01357
Date accepted:25 July 2021
Date deposited:12 August 2021
Date of first online publication:09 August 2021
Date first made open access:09 August 2022

Save or Share this output

Export:
Export
Look up in GoogleScholar