Critical investigation of the long-term integrity of sustainable anti-corrosion coatings in static and dynamic humid environments

This study evaluated the water-induced degradation of epoxy-based coatings modified with eco-friendly corrosion inhibitors in static and dynamic humid environments, designed to replicate conditions characteristic of marine exposure. Using electrochemical impedance spectroscopy, surface and interfacial analyses, and mechanical testing, degradation of coatings applied on mild steel samples was assessed under stagnant, flowing, and salt-spray conditions. The degradation trend of coatings significantly increased in salt-spray tests through elevated temperature (35 °C) and water-induced degradation of the epoxy matrix. Hydrodynamic flow also accelerated degradation through enhanced water diffusion and stresses arising from both water absorption and flow. Pure epoxy coatings lost their protective properties after 90 days in stagnant solutions, 77 days in flowing solutions, and 56 days in salt spray tests. Incorporating calcium borosilicate (CBS), zinc calcium strontium aluminum orthophosphate silicate hydrate (ZCP), and strontium phosphosilicate (SPS) into the epoxy matrix delayed water uptake and coating delamination. CBS-modified coatings extended protection more than twofold in stagnant and flowing environments, with performance in salt spray comparable to pure epoxy. ZCP-pigmented coatings preserved their integrity in stagnant conditions and doubled protection in salt spray and flowing scenarios. SPS-pigmented coatings demonstrated exceptional durability, maintaining integrity for over 210 days across all conditions. These results highlight the critical role of selecting inhibitors suited to specific environmental conditions and demonstrate that water-induced degradation of epoxy coatings is governed by multifaceted interplay of the coating's mechanical properties, interfacial electrochemical activities, and changes in the chemistry of environment at the metal-coating interface. • Epoxy-based coatings degradation assessed in static and dynamic humid environments. • Humidity exposure altered surface roughness, adhesion strength, and permeability. • Eco-friendly inhibitors reduced water uptake and improved corrosion resistance. • Inhibitor performance varied across environments, affecting long-term performance. • SPS-epoxy maintained corrosion resistance despite mechanical and structural changes.

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Publication Details

Journal
Progress in Organic Coatings
Published
2025-03-30
DOI
https://doi.org/10.1016/j.porgcoat.2025.109276
Citations
2
Primary Topic
Corrosion Behavior and Inhibition
Type
article
Field-Weighted Citation Impact
1.04
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article

Critical investigation of the long-term integrity of sustainable anti-corrosion coatings in static and dynamic humid environments

M. Gaier, Ehsan Bakhshandeh, Zhila Russell, Kevin P. Plucknett et al.
2 citations
Progress in Organic Coatings
Corrosion Behavior and Inhibition
1.04
article

Critical investigation of the long-term integrity of sustainable anti-corrosion coatings in static and dynamic humid environments

M. Gaier, Ehsan Bakhshandeh, Zhila Russell, Kevin P. Plucknett, Kazem Sabet-Bokati
article en
2 citations

Abstract

This study evaluated the water-induced degradation of epoxy-based coatings modified with eco-friendly corrosion inhibitors in static and dynamic humid environments, designed to replicate conditions characteristic of marine exposure. Using electrochemical impedance spectroscopy, surface and interfacial analyses, and mechanical testing, degradation of coatings applied on mild steel samples was assessed under stagnant, flowing, and salt-spray conditions. The degradation trend of coatings significantly increased in salt-spray tests through elevated temperature (35 °C) and water-induced degradation of the epoxy matrix. Hydrodynamic flow also accelerated degradation through enhanced water diffusion and stresses arising from both water absorption and flow. Pure epoxy coatings lost their protective properties after 90 days in stagnant solutions, 77 days in flowing solutions, and 56 days in salt spray tests. Incorporating calcium borosilicate (CBS), zinc calcium strontium aluminum orthophosphate silicate hydrate (ZCP), and strontium phosphosilicate (SPS) into the epoxy matrix delayed water uptake and coating delamination. CBS-modified coatings extended protection more than twofold in stagnant and flowing environments, with performance in salt spray comparable to pure epoxy. ZCP-pigmented coatings preserved their integrity in stagnant conditions and doubled protection in salt spray and flowing scenarios. SPS-pigmented coatings demonstrated exceptional durability, maintaining integrity for over 210 days across all conditions. These results highlight the critical role of selecting inhibitors suited to specific environmental conditions and demonstrate that water-induced degradation of epoxy coatings is governed by multifaceted interplay of the coating's mechanical properties, interfacial electrochemical activities, and changes in the chemistry of environment at the metal-coating interface. • Epoxy-based coatings degradation assessed in static and dynamic humid environments. • Humidity exposure altered surface roughness, adhesion strength, and permeability. • Eco-friendly inhibitors reduced water uptake and improved corrosion resistance. • Inhibitor performance varied across environments, affecting long-term performance. • SPS-epoxy maintained corrosion resistance despite mechanical and structural changes.

Progress in Organic CoatingsVol. 204
Dalhousie University (CA), Communications Security Establishment (CA), Advanced Coatings (Belgium) (BE)
Life in Land
Openalex Percentile: Top 27%
Corrosion Behavior and Inhibition
1.04
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