Abstract

The surface charge properties of Berea sandstone (and its major components), Indiana limestone and Baker dolomite in concentrated electrolyte solutions were investigated. This was accomplished by crushing the rocks into fine particles which were then suspended in aqueous solutions to permit electrokinetic measurements. The electrophoretic mobilities (zeta potentials) of the particles were determined as functions of pH, ionic strength and ionic composition in ranges that are of interest in enhanced oil recovery (EOR) processes. To achieve this, it was necessary to investigate electrokinetic behaviour at much higher ionic strengths than are normally reported in the literature. In general, the Berea sandstone and its constituent quartz and clay fractions adopted a negative charge in the aqueous solutions, the magnitude of which was significantly influenced by pH, the ionic strength and the degree of hardness in the electrolyte solution. Under some conditions severe charge reduction and charge reversal were observed. The limestone and dolomite were more dramatically influenced by both pH and the presence of multivalent cations. The magnitude of the surface charges varied considerably and could adopt positive or negative surface charges depending on the solution properties. The sensitivity of these reservoir minerals to small changes in solution properties carries potentially serious implications for any EOR process whose efficiency depends indirectly on the rock surface charge. Examples would include the adsorption of surfactants, particularly ionic and amphoteric surfactants, and the chemical mobilization of fines causing permeability damage.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.