For the first time, organic tannic acid (TA) molecules and then inorganic praseodymium (Pr) cations as corrosion inhibitors were successfully loaded into a zeolitic imidazolate framework (ZIF8)-type porous coordination polymer (PCP) decorated on molybdenum disulfide, MoS, (MS)-based transition metal dichalcogenides (TMDs) to create novel hybrid mesoporous Pr/TA-ZIF8@MS nanoreservoirs. Thereafter, the hybrid nanoreservoirs were embedded into the epoxy matrix for the preparation of smart pH-triggered nanocoatings. Characterizations of the Pr/TA-ZIF8@MS nanoreservoirs via Fourier transform infrared (FT-IR), X-ray diffraction (XRD), thermogravimetric (TG), Brunauer-Emmett-Teller (BET), and field emission-scanning electron microscopy (FE-SEM)/energy-dispersive X-ray spectroscopy (EDS) experiments confirmed the fabrication of mesoporous structures comprising Pr/TA interfacial interactions with ZIF8-decorated MS nanoplatelets possessing high thermal stability and compact/dense configuration features with a framework reorientation. A remarkable smart release of the inhibited cations (Pr and Zn) in the presence of inbuilt TA at both acidic and alkaline media was achieved under inductively coupled plasma (ICP) examination. The superior pH-triggered self-healing inhibition through the smart controlled-release of Pr, tannate, Zn, and imidazole inhibited species/complexes from EP/Pr-TA-ZIF8@MS via ligand exchange was obtained from electrochemical impedance spectroscopy (EIS) assessments of the scratched coatings during 72 h of saline immersion. In addition, the long-term barrier-induced corrosion prevention (log || = 10.49 Ω·cm after 63 days) of the EP/Pr-TA-ZIF8@MS was actualized. Moreover, efficient increments of the coating cross-link density (56.45%), tensile strength (63.6%), and toughness value (56.5%) compared to the Neat epoxy coating revealed noticeable thermomechanical properties of the EP/Pr-TA-ZIF8@MS.

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