Abstract
Surfactants are very important surface-active agents in implementation of chemical enhanced oil recovery for oil-water interfacial tension and wettability alteration. However, the high adsorption of surfactant on reservoir rock reduces the efficiency of surfactant flooding. Conventionally, inorganic alkali has been introduced to reduce adsorption of surfactant, but alkali will lead to the formation of emulsion, formation damage and scaling. Therefore, lignosulfonate, a sacrificial agent has been introduced as an alternative to inorganic alkali. In this paper, the critical micelle concentration (CMC) and dynamic interfacial tension (IFT) behavior of a pure and binary system of internal olefin sulfonate (IOS) and lignosulfonate (LS) at brine-decane interfaces are determined by using a spinning drop method. The physicochemical properties of pure and binary of IOS and LS system are determined by conductivity and pH measurements. The CMC value of IOS in 3.5 wt% brine salinity is higher compared to LS due to the isomeric branched of IOS which can occupy a larger area per molecules. The dynamic interfacial tension of IOS shows the fast adsorption of surfactant molecules to the brine-decane interfaces. This is indicated by the fast equilibrium interfacial tension reached by IOS. In comparison, the LS pure system shows decreasing behavior of dynamic interfacial tension. The fast adsorption at the interfaces is only reached for higher LS concentrations. The synergy effect between IOS and LS system shows a reduction in the interfacial value with LS optimum concentration of 0.6 wt%. The drop in conductivity and pH values indicated the development of a tightly packed lamellar liquid crystalline structure. These physicochemical properties are in agreement with the dynamic interfacial tension behavior of the IOS and LS system. This study has demonstrated the significant impact of the LS addition in reducing the dynamic interfacial tension of the surfactant system.
Published Version
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