Film morphology, surface compositions and hydrophobic properties of N-β-aminoethyl-γ-aminopropyl polysiloxane (ASO-1) coated on regenerated cellulose (cel) substrate surface (ASO-1/cel) were investigated and studied by atomic force microscopy, X-ray photoelectron spectroscopy and other techniques. Influenced by the irregularities of cel substrate, ASO-1/cel showed a very similar microscopic morphology to the cel. In addition, the ASO-1/cel surface was hydrophobic. There were strongly hydrogen-bonded linkages at the interface between ASO-1 and cel. All the data indicate that ASO-1 molecules interact with the regenerated cellulose in such a way that the hydrophobic silicon methyl (Si-CH₃) groups are oriented towards the air, while the Si—O dipole bonds as well as the polar amino groups are aligned towards the interface of the cellulose substrate.

To design a mechanically stable and superhydrophobic coating, a polyhedral oligomeric silsesquioxane (POSS)-containing poly(perfluoropolyether)methacrylate (PFPEM) hybrid copolymer (PFPEM–POSS) was synthesized via a free-radical solution polymerization with PFPEM, 1H,1H,2H,2H-perfluorooctyl acrylate, methyl (meth)acrylate, n-butyl acrylate, hydroxypropyl acrylate, methacryloxy propyl trimethoxy silane, and methacrylisobutyl POSS; and azobisisobutyronitrile as an initiator. Hydrophobic coatings were formed on substrates by a facile one-step dip-coating method in a solution mixture of diethylene glycol dimethyl ether with the PFPEM–POSS hybrid copolymer. The chemical structure of the PFPEM–POSS copolymer and the surface morphology and performance of the PFPEM–POSS coatings were investigated. The results indicate that, under POSS aggregation via the fluorophilic/oleophilic co-monomer phase separation and owing to the low-surface-energy poly(perfluoropolyether)methacrylate incorporated into the copolymer, PFPEM–POSS exhibited a hierarchical micro-nano roughness in atomic force microscopy observations and provided the treated substrates with excellent hydrophobicity and abrasion resistance. As a result, the water contact angle reached 152.3° on the treated glass.

Corrosion of structural parts not only reduces the service life of the equipment but also causes safety accidents, so building a long-lasting anti-corrosion coating on its surface is the key to solving this problem. Under the action of alkali catalysis, n-octyltriethoxysilane (OTES), dimethyldimethoxysilane (DMDMS), and perfluorodecyltrimethoxysilane (FTMS) hydrolyzed and polycondensed co-modified graphene oxide (GO), modified to synthesize a self-cleaning superhydrophobic material fluorosilane-modified graphene oxide (FGO). The structure, film morphology, and properties of FGO were systematically characterized. The results showed that the newly synthesized FGO was successfully modified by long-chain fluorocarbon groups and silanes. FGO presented an uneven and rough morphology on the substrate surface, the water contact angle was 151.3°, and the rolling angle was 3.9°, which caused the coating to exhibit excellent self-cleaning function. Meanwhile, the epoxy polymer/fluorosilane-modified graphene oxide (E-FGO) composite coating adhered to the carbon structural steel’s surface, and its corrosion resistance was detected by the Tafel curve and EIS impedance. It was found that the current density of the 10 wt% E-FGO coating (I_corr) was the lowest (1.087 × 10⁻¹⁰ A/cm²), which was approximately 3 orders of magnitude lower than that of the unmodified epoxy coating. This was primarily due to the introduction of FGO, which formed a continuous physical barrier in the composite coating and gave the composite coating excellent hydrophobicity. This method might provide new ideas for advances in steel corrosion resistance in the marine sector.