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The enhancement of dispersion stability and interfacial compatibility of nanomaterials within aqueous epoxy matrices represents a pivotal strategy for augmenting the protective performance and corrosion resistance of coatings. In this study, Ti 3 C 2 T x Mxene functionalized with sodium alginate (TSA) was obtained by introducing sodium alginate (SA) into Ti 3 C 2 T x Mxene (T) to improve the corrosion resistance of aqueous epoxy coatings (EP). The dispersion stability of TSA in aqueous medium was quantitatively assessed via ζ-potential measurements, revealing a significant enhancement in stability compared to the reference material T. The long-term stability of TSA/EP composite coatings was systematically evaluated via electrochemical impedance spectroscopy (EIS). Notably, the charge transfer resistance ( R c ) remained at 5 × 10 7 Ω·cm 2 after a 60-day accelerated aging test, exhibiting exceptional electrochemical durability. Compared with pure EP coating, this value is improved by 2 orders of magnitude. The improvement is attributed to the fact that active −COOH and −OH groups on the surface of SA enhance the interactions between T nanosheets and EP matrix. Specifically, these functional groups form hydrogen bonds or chemical bonds at the interface. Such interfacial bonding mechanisms enhance the compatibility and interfacial adhesion between T and the EP matrix. These conclusions are further supported by manual scratching experiments. The accessibility and greenness of SA provide a simple and environmentally friendly way of thinking for modifying T.
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Hu et al. (2025) studied this question.
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