Adaptive Coatings with Anticorrosion and Antibiofouling Properties

Biofouling on surfaces immersed in aquatic environment induces catastrophic corrosion of metallic materials in petrochemical infrastructures, maritime facilities, and power plants. To combat the synergistic effect of biofouling and corrosion on the deterioration of metallic materials, smart coatings possessing a dual function of antibiofouling and anticorrosion properties are needed. Herein, redox-responsive copolymer conjugates are synthesized and employed as coatings with the dual function of biofouling and corrosion mitigation. The dual function of copolymers is attributed to fluorinated units and the corrosion inhibitor 2-mercaptobenzothiazole (MBT) conjugated via disulfide linkages. Indeed, the disulfide linkages can be cleaved in a reducing environment, yielding controlled release of the corrosion inhibitor MBT during corrosion process. The antibiofouling action against protein adsorption and algal attachment is enabled by cooperation of the repellent characteristic of fluorinated moieties and the biocidal effect of conjugated MBT.     

Synthesis and properties of LaNi<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Fe<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>3−δ</Subscript> as cathode materials in SOFC

The synthesis of LaNi_{1− x} Fe _x O_3−δ (LNF) perovskites with x = 0.0–1.0, for use as cathode materials for an IT-SOFC, was investigated using four combustion methods, Water Citrate (WC), Modified Water Citrate (MWC), Nitric Citrate (NC), and Modified Nitric Citrate (MNC). The structures and homogeneities of the synthesized powders were examined using an XRD, and the particle sizes were examined using an SEM and a particle size analyzer. All four combustion methods gave the single phase perovskites with the same structure. The main difference was shown in a particle size that the smallest to the largest sizes were obtained from MNC, MWC, NC, and WC, respectively. In this LNF series, as x is 0–0.5, the crystal structure is cubic and rhombohedral at the calcination temperature of 700 and 900 °C, respectively. Further investigation indicated that the cubic structure changed to rhombohedral structure at 900 °C, and was stable up to 1200 °C. As x is 0.6–1.0, the crystal structure is in orthorhombic phase when calcined between 700 and 1000 °C. This orthorhombic phase decomposed above 1100 °C. From the XRD and SEM–EDX results, LaNi_0.6Fe_0.4O_3−δ (LNF64) has a good chemical compatibility with 8YSZ from room temperature up to 900 °C. In addition, its thermal expansion coefficient is 13.2 × 10⁻⁶ K⁻¹ close to that of 8 mol% Y₂O₃ (8YSZ). Therefore, LNF64 also has a good physical compatibility with 8YSZ.