Combination of dopamine and tyrosinase as a green corrosion inhibitor for carbon steelShow others and affiliations
2026 (English)In: Corrosion Science, ISSN 0010-938X, E-ISSN 1879-0496, Vol. 260, article id 113523Article in journal (Refereed) Published
Abstract [en]
This study investigates the combination of dopamine (DA) and tyrosinase (TYR) for corrosion protection of carbon steel in acidic conditions, focusing on corrosion protection behavior and film formation mechanisms. Confocal Raman microscopy analysis demonstrated that DA forms a thin protective film on carbon steel through complexation with Fe ions, preferably at defect sites, thereby transforming mixed Fe oxides to Fe(catechol)3, while TYR promotes DA oxidation and enhances the complexation. Surface coverage of Fe(catechol)3 increases from 37 % at 10 min to 89 % at 60 min of exposure in the DA/TYR solution. Inductively coupled plasma-optical emission spectroscopy (ICP-OES) measurements showed a 25 % reduction in Fe release after 48 h in the DA/TYR solution. X-ray photoelectron spectroscopy (XPS) analysis revealed that TYR promotes oxidation from Fe2+ to Fe3+ at the surface, resulting in a thinner yet more protective DA-Fe complexation film. The DA/TYR system increased corrosion resistance by 47 % after 24 h, primarily attributed to the rapid and extensive formation of Fe (catechol)3 complexes between DA and Fe ions released from the substrate, further strengthened by TYR. This bio-inspired and green corrosion inhibitor strategy, combining DA's metal-binding affinity with TYR's enzymatic oxidation capability, provides a scalable and non-toxic strategy for effective corrosion protection.
Place, publisher, year, edition, pages
Elsevier BV , 2026. Vol. 260, article id 113523
Keywords [en]
Dopamine, Tyrosinase, Bio-inspired film, Corrosion inhibition, Complexation
National Category
Surface- and Corrosion Engineering
Identifiers
URN: urn:nbn:se:kth:diva-377274DOI: 10.1016/j.corsci.2025.113523ISI: 001637549900001Scopus ID: 2-s2.0-105023953255OAI: oai:DiVA.org:kth-377274DiVA, id: diva2:2041217
Note
QC 20260224
2026-02-242026-02-242026-02-24Bibliographically approved