4.5 Article

Study of Chelating Agent-Surfactant Interactions on the Interphase as Possibly Useful for the Well Stimulation

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ENERGIES
卷 16, 期 4, 页码 -

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MDPI
DOI: 10.3390/en16041679

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chelating agents; EDTA; surfactant; IFT; molecular dynamics

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The application of chelating agents in enhanced oil recovery (EOR) and well stimulation is growing rapidly. However, chelating agents have drawbacks, including high interfacial tension (IFT). This paper investigates the interaction between a chelating agent (ethylenediaminetetraacetic acid, EDTA) and anionic and cationic surfactants (sodium dodecyl sulfate, SDS and dodecyl trimethynlammonium bromide, DTAB) through experimental and theoretical methods. The results show that the addition of chelating agents decreases IFT and lowers the critical micelle concentration of surfactants, indicating a salting-out effect. Molecular dynamics simulations reveal closer packing of the surfactant layer and decreased hydration of head groups, with specific attractive interactions observed with SDS. These findings can be useful for selecting appropriate fluids for real-field operations.
Chelating agents' application for EOR and well stimulation is fast growing nowadays. However, reagents of this class have some drawbacks, with high values of interfacial tension (IFT) being among them. IFT may be lowered with the addition of surfactants; however, the simultaneous application of chelating agents and surfactants has not yet been widely studied. This paper focuses on the experimental and theoretical investigation of the interaction between chelating agent (ethylenediaminetetraacetic acid, EDTA) and surfactants of anionic and cationic types (sodium dodecyl sulfate, SDS, and dodecyl trimethynlammonium bromide, DTAB). IFT measurement was performed at ambient conditions, with normal octane being as the reference hydrocarbon to eliminate the temperature and salinity effects and compare surfactant-containing systems. The experimental results show that chelating agents' addition to the solutions of surfactants leads to a decrease in IFT value. Moreover, surfactants' critical micelle concentration is lowered, whereas their effectiveness and efficiency are increased, which points to the salting-out nature of chelating agents. Molecular dynamics reveal that chelating agent addition causes closer packing of surfactant layer, the decrease in head groups' hydration, and, at least in the case of SDS, specific surfactant-chelating agent attractive interaction. These molecular-level insights, experimental dependencies, and the combined methodology may be useful for the proper selection of fluids for real-field operations.

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