The massive and long-term service of 5083 aluminum alloy (AA5083) is restricted by several shortcomings in marine and industrial environments, such as proneness to localized corrosion attack, surface contamination, etc. Herein, we report a facile and cost-effective strategy to transform intrinsic hydrophilicity into water-repellent superhydrophobicity, combining fluorine-free chemisorption of a hydrophobic agent with etching texture. Dual-scale hierarchical structure, surface height relief and surface chemical elements were studied by field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS), successively. Detailed investigations of the wetting property, self-cleaning effect, NaCl-particle self-propelling, corrosion and long-term behavior of the consequent superhydrophobic AA5083 surface were carried out, demonstrating extremely low adhesivity and outstanding water-repellent, self-cleaning and corrosion-resisting performance with long-term stability. We believe that the low cost, scalable and fluorine-free transforming of metallic surface wettability into waterproof superhydrophobicity is a possible strategy towards anti-contamination and marine anti-corrosion.

A novel visible light-driven AgBr/AgCl@ZIF-8 catalyst was synthesized by a simple and rapid method. The composition and structure of the photocatalyst were characterized by XRD, SEM, UV-DRS, and XPS. It could be observed that the 2-methylimidazole zinc salt (ZIF-8) exhibited the rhombic dodecahedron morphology with the AgCl and AgBr particles evenly distributed around it. The composite photocatalyst AgBr/AgCl@ZIF-8 showed good photocatalytic degradation and antibacterial properties. The degradation rate of RhB solution was 98%, with 60 min of irradiation of visible light, and almost all P. aeruginosaudomonas aeruginosa (P. aeruginosa), Staphylococcus aureus (S. aureus), and Escherichia coli (E. coli) were inactivated under the irradiation of 90 min. In addition, the prepared catalyst had excellent stability and reusability. Based on the free radical capture experiment, ·O₂⁻ and h⁺ were believed to be the main active substances, and possible photocatalytic degradation and sterilization mechanisms of AgBr/AgCl@ZIF-8 were proposed.

A 2D MoS₂ nanosheet was prepared and treated by sodium dodecyl benzene sulfonate (SDBS) to fabricate 2D MoS₂/SDBS composite (2D-MSC) coating on carbon steel. The anticorrosion performance of coating was comprehensively investigated.

Corrosion of aluminum alloys (Al alloys) has been a ubiquitous problem, and this seriously restricts its range of applications.

Given the corrosion tendency of the natural oxide film of aluminum alloys, micro arc oxidation (MAO) treatment is used as an efficient and economic method to enhance the corrosion resistance. However, irregular voids, pores, and micro cracks are easily formed during the MAO process, which are harmful to the anti-corrosion property of MAO coatings. In this paper, binary additives of electrolytes, including (NaPO₃)₆ and H₃BO₃, were used to obtain MAO coatings with improved thickness and compact microstructures on 6061 aluminum alloys. The as-prepared coatings were investigated using a thickness meter, scanning electron microscope (SEM), X-ray diffractometer (XRD), and electrochemical impedance spectroscope (EIS). The results showed that the coordinated influence of the binary additives could change the discharge behaviors and micro morphologies of the MAO coatings compared to the base silicate electrolyte. A thicker and stronger MAO coating could be achieved, which was mainly composed of Al₂O₃ phases. The EIS tests revealed that the corrosion current density of the obtained optimal MAO coating decreased by three orders of magnitude from 1.209 × 10⁻⁶ A·cm⁻² to 2.981 × 10⁻⁹ A·cm⁻². We believe that the binary additive-enhanced MAO coatings could provide a promising anti-corrosion solution in various applications.