An understanding of the interaction of calcareous deposits and biofoulants on the corrosion performance of steel during the fouling stage is both interesting and necessary. So, the effects of these factors on Q235 carbon steel were investigated and discussed for 20 weeks under real ocean conditions. The results indicate that calcareous deposits are favorable for the attachment of marine microorganisms. However, macroorganisms prefer adhering directly to the substrate. The generations of calcareous deposits have priority over the biofilm attachment under the condition of cathodic protection. Calcareous deposits can prevent steel against corrosion for four weeks without cathodic protection.

Juglone (5-hydroxy-1,4-naphthalenedione), a natural compound derived from walnut husks, was investigated as a sustainable dual-function antibacterial agent and corrosion inhibitor for Q235 steel in sulfate-reducing bacteria (SRB)-containing seawater. Juglone was synthesized via an improved one-pot method, and its performance was evaluated through antibacterial assays, weight loss measurements, surface characterization (SEM, XPS, XRD), and electrochemical techniques (EIS, PDP). Juglone exhibited potent antibacterial activity against Desulfovibrio sp., with a minimum inhibitory concentration (MIC) of 40 mg/L. At 20 mg/L (0.5 MIC) and 40 mg/L (1 MIC), it effectively suppressed bacterial growth and metabolism, mitigating corrosion. At 80 mg/L (2 MIC), a dual-action mechanism was observed: strong antibacterial effect combined with chemical reaction with H₂S, a corrosive SRB metabolite, forming a protective thiol-containing film on the steel surface. This reduced the corrosion current density from 3.16 × 10⁻⁵ A/cm² to 7.94 × 10⁻⁷ A/cm², achieving an inhibition efficiency of 97.5%. Juglone represents a promising green alternative to conventional toxic antibacterial agents, aligning with circular economy principles.

The effects of organic metabolites produced by a sulfate-reducing prokaryote (SRP) in seawater on the anode corrosion process of magnesium alloy were analyzed by open circuit potential, electrochemical impedance spectroscopy, polarization curve, and other electrochemical methods, combined with scanning electron microscopy and X-ray diffraction. It was found that the product film produced by magnesium alloy anode corrosion was not dense, and the surface of the magnesium anode substrate was exposed during the corrosion process. The corrosion of magnesium anode matrix was accelerated by the simulation of different organic metabolites including mannose, glucuronic acid, and glucose. Thus, the synergistic effect of various metabolites produced by SRP in the corrosion process of magnesium alloy may be considered in future studies.