Bioinspired Graphene Oxide-Magnetite Nanocomposite Coatings as Protective Superhydrophobic Antifouling Surfaces.

Antifouling (AF) nanocoatings made of polydimethylsiloxane (PDMS) are more cost-efficient and eco-friendly substitutes for the already outlawed tributyltin-based coatings. Here, a catalytic hydrosilation approach was used to construct a design inspired by composite mosquito eyes from non-toxic PDMS nanocomposites filled with graphene oxide (GO) nanosheets decorated with magnetite nanospheres (GO-Fe3O4 nanospheres). Various GO-Fe3O4 hybrid nanofillers were dispersed into the PDMS resin through a solution casting method to evaluate the structure-property relationship. A simple coprecipitation procedure was used to fabricate magnetite nanospheres with an average diameter of 30-50 nm, a single crystal structure, and a predominant (311) lattice plane. The uniform bioinspired superhydrophobic PDMS/GO-Fe3O4 nanocomposite surface produced had a micro-/nano-roughness, low surface-free energy (SFE), and high fouling release (FR) efficiency. It exhibited several advantages including simplicity, ease of large-area fabrication, and a simultaneous offering of dual micro-/nano-scale structures simply via a one-step solution casting process for a wide variety of materials. The superhydrophobicity, SFE, and rough topology have been studied as surface properties of the unfilled silicone and the bioinspired PDMS/GO-Fe3O4 nanocomposites. The coatings' physical, mechanical, and anticorrosive features were also taken into account. Several microorganisms were employed to examine the fouling resistance of the coated specimens for 1 month. Good dispersion of GO-Fe3O4 hybrid fillers in the PDMS coating until 1 wt % achieved the highest water contact angle (158° ± 2°), the lowest SFE (12.06 mN/m), micro-/nano-roughness, and improved bulk mechanical and anticorrosion properties. The well-distributed PDMS/GO-Fe3O4 (1 wt % nanofillers) bioinspired nanocoating showed the least biodegradability against all the tested microorganisms [Kocuria rhizophila (2.047%), Pseudomonas aeruginosa (1.961%), and Candida albicans (1.924%)]. We successfully developed non-toxic, low-cost, and economical nanostructured superhydrophobic FR composite coatings for long-term ship hull coatings. This study may expand the applications of bio-inspired functional materials because for multiple AF, durability and hydrophobicity are both important features in several industrial applications.

A comparative study between two novel silicone/graphene-based nanostructured surfaces for maritime antifouling.

Two novel superhydrophobic nanocomposite series of polydimethylsiloxane (PDMS) enriched with reduced graphene oxide (RGO) and graphene oxide/boehmite nanorods (GO-γ-AlOOH) nanofillers were synthesized as maritime fouling-release (FR) surfaces. Controlling the nanofillers' structures and distribution in the silicone matrix influenced the self-cleaning and antifouling properties. γ-AlOOH nanorods had a single crystallinity with an average diameter of 10-20 nm and < 200 nm length. A hydrothermal method was used to prepare RGO, while the chemical deposition method was used to synthesis GO-γ-AlOOH nanocomposites for use as fouling-release coating materials. For studying the synergetic effects of graphene-based materials on the surface, mechanical, and FR features, these nanofillers were dispersed in the silicone matrix using the solution casting method. The hydrophobicity and antifouling properties of the surface were studied using water contact angle (WCA), scanning electron, and atomic force microscopes (SEM and AFM). Coatings' roughness, superhydrophobicity, and surface mechanical properties all improved for the homogeneity of the dispersion of the nanocomposite. Laboratory assessments were carried out for 30 days using selected microorganisms to determine the antifouling effects of the coating systems. PDMS/GO-γ-AlOOH nanorod composite had better antibacterial activity than PDMS/RGO nanocomposite against different bacterial strains. This is caused by the high surface area and stabilizing effects of the GO-γ-AlOOH hybrid nanofillers. The PDMS/GO-γ-AlOOH nanorod composite (3 wt%) had the lowest biodegradability percentage (1.6%) and the microbial endurability percentages for gram-positive, gram-negative, and fungi were 86.42%, 97.94%, and 85.97%, respectively. A field trial in natural seawater was conducted to confirm the coatings' FR performance based on the screening process and image analysis for 45 days in a tropical area. The most profound superhydrophobic antifouling nanostructured coating was the homogeneity of the GO-γ-AlOOH (3 wt%) dispersion, which had a WCA of 151° and a rough surface.

Engineering nanoscale hierarchical morphologies and geometrical shapes for microbial inactivation in aqueous solution.

Here, we study the effect of hierarchical and one-dimensional (1D) metal oxide nanorods (H-NRs) such as γ-Al2O3, ß-MnO2, and ZnO as microbial inhibitors on the antimicrobial efficiency in aqueous solution. These microbial inhibitors are fabricated in a diverse range of nanoscale hierarchical morphologies and geometrical shapes that have effective surface exposure, and well-defined 1D orientation. For instance, γ-Al2O3 H-NRs with 20 nm width and ˂0.5 µm length are grown dominantly in the [400] direction. The wurtzite structures of ß-MnO2 H-NRs with 30 nm width and 0.5-1 µm length are preferentially oriented in the [100] direction. Longitudinal H-NRs with a width of 40 nm and length of 1 µm are controlled with ZnO wurtzite structure and grown in [0001] direction. The antimicrobial efficiency of H-NRs was evaluated through experimental assays using a set of microorganisms (Gram-positive Staphylococcus aureus, Bacillus thuriginesis, and Bacillus subtilis) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. Minimal inhibitory and minimum bactericidal concentrations (MIC and MBC) were determined. These 1D H-NRs exhibited antibacterial activity against all the used strains. The active surface exposure sites of H-NRs play a key role in the strong interaction with the thiol units of vital bacterial enzymes, leading to microbial inactivation. Our finding indicates that the biological effect of the H-NR surface planes on microbial inhibition is decreased in the order of [400]-γ-Al2O3 > [100]-ß-MnO2 > [0001]-ZnO geometrics. The lowest key values including MIC (1.146 and 0.250 µg/mL), MBC (1.146, 0.313 µg/mL), and MIC/MFC (0.375 and 0.375 µg/mL) are achieved for [400]-plane γ-Al2O3 surfaces when tested against Gram-positive and -negative bacteria, respectively. Among the three H-NRs, the smallest diameter size and length, the largest surface area, and the active exposure [400] direction of γ-Al2O3 H-NRs could provide the highest microbial inactivation.

Blade-like structure of graphene oxide sheets decorated with cuprous oxide and silicon carbide nanocomposites as bactericidal materials.

In the current work, graphene oxide nanosheets decorated with cuprous oxide nanospheres (GO/Cu2O) and with silicon carbide nanowires (GO/SiC) were synthesized and controlled for using as blade-like antibacterial agents. Preparation of GO sheets with <2 nm thickness was performed through a modified Hummers approach. Controlled Cu2O spheres with a mean size of 40 nm were prepared through a wet-chemical approach. For comparative studies, a single step chemical deposition method was used to prepare GO/Cu2O and GO/SiC nanocomposites for using as antibacterial active materials. The nanomaterials' biological behavior and bacterial-resistance were assessed via selected Gram-negative and gram-positive bacteria and yeast strains. GO/Cu2O nanocomposite exhibited higher antibacterial activity against different bacterial strains than GO/SiC composite. GO/Cu2O exhibited average activity index, minimum inhibitory concentration (MIC) values, and viable cell numbers of 1.523, 10.438 µg/mL, and 82.962% for Bacillus subtilis, Brevibacillus brevis and Bacillus thuriginesis), 1.453, 32.00 µg/mL, and 68.418% for Pseudomonas aeruginosa and Escherichia coli) and 68.608% for Candida albicans, respectively. The antimicrobial efficiency of the blade-like GO/Cu2O was elucidated by scanning electron microscopy through the complete wrapping of the cell membranes and disrupting their shape morphology. GO nanosheets could increase the Cu2O dispersion in the aqueous solution, prevent their agglomeration, and stabilize its action in aqueous solution with high microbial toxicity.

Silicone/Ag@SiO2 core-shell nanocomposite as a self-cleaning antifouling coating material.

The effects of Ag@SiO2 core-shell nanofiller dispersion and micro-nano binary structure on the self-cleaning and fouling release (FR) in the modelled silicone nano-paints were studied. An ultrahydrophobic polydimethylsiloxane/Ag@SiO2 core-shell nanocomposite was prepared as an antifouling coating material. Ag@SiO2 core-shell nanospheres with 60 nm average size and a preferential {111} growth direction were prepared via a facile solvothermal and a modified Stöber methods with a controlled shell thickness. Ag@SiO2 core-shell nanofillers were inserted in the silicone composite surface via solution casting technique. A simple hydrosilation curing mechanism was used to cure the surface coating. Different concentrations of nanofillers were incorporated in the PDMS matrix for studying the structure-property relationship. Water contact angle (WCA) and surface free energy determinations as well as atomic force microscopy and scanning electron microscope were used to investigate the surface self-cleaning properties of the nanocomposites. Mechanical and physical properties were assessed as durability parameters. A comparable study was carried out between silicone/spherical Ag@SiO2 core-shell nanocomposites and other commercial FR coatings. Selected micro-foulants were used for biological and antifouling assessments up to 28 days. Well-distributed Ag@SiO2 core-shell (0.5 wt%) exhibited the preferable self-cleaning with WCA of 156° and surface free energy of 11.15 mN m-1.

Data on photo-nanofiller models for self-cleaning foul release coating of ship hulls.

The data presented in this article are related to the research article entitled "Smart photo-induced silicone/TiO2 nanocomposites with dominant [110] exposed surfaces for self-cleaning foul-release coatings of ship hulls" (Selimet al., 2016) [1]. This article reports on successfully designing and controlling TiO2 spherical single crystal photo-nanofillers and indicating evidence of fouling resistance after stimulation through UV radiation exposure. These data also reveal that the influence of well-dispersed spherical TiO2 nanoparticles (NPs) into the polymer matrix surface features on the prepared fouling release (FR) coating. Single crystal TiO2 nanospheres have played a large role in the scenario of photocatalysis due to its cost effectiveness, inert nature and photo stability. The model output and the surface and mechanical behavior data of the fabricated UV-irradiated silicone-based FR nanocoatings are made publicly available through analyzing nanocomposite topology, superhydrophilicity and self-cleaning efficiency in order to enable critical analysis of the tailored model. It also investigates the photo-bactericidal effect confirmed through biofilm coverage data disability. The modeled nanocomposites were subjected to comparable studies with other published models so as to understand how different UV-irradiated nano-scale parameters propagate and affect bulk film response.