Sonochemical synthesis of bioinspired graphene oxide-zinc oxide hydrogel for antibacterial painting on biodegradable polylactide film.

Graphene oxide nanosheet (GO) is a multifunctional platform for binding with nanoparticles and stacking with two dimensional substrates. In this study, GO nanosheets were sonochemically decorated with zinc oxide nanoparticles (ZnO) and self-assembled into a hydrogel of GO-ZnO nanocomposite. The GO-ZnO hydrogel structure is a bioinspired approach for preserving graphene-based nanosheets from van der Waals stacking. X-ray diffraction analysis (XRD) showed that the sonochemical synthesis led to the formation of ZnO crystals on GO platforms. High water content (97.2%) of GO-ZnO hydrogel provided good property of ultrasonic dispersibility in water. Ultraviolet-visible spectroscopic analysis (UV-vis) revealed that optical band gap energy of ZnO nanoparticles (∼3.2 eV) GO-ZnO nanosheets (∼2.83 eV). Agar well diffusion tests presented effective antibacterial activities of GO-ZnO hydrogel against gram-negative bacteria (E. coli) and gram-positive bacteria (S. aureus). Especially, GO-ZnO hydrogel was directly used for brush painting on biodegradable polylactide (PLA) thin films. Graphene-based nanosheets with large surface area are key to van der Waals stacking and adhesion of GO-ZnO coating to the PLA substrate. The GO-ZnO/PLA films were characterized using photography, light transmittance spectroscopy, coating stability, scanning electron microscopy (SEM), energy-dispersive x-ray spectroscopic mapping (EDS), antibacterial test and mechanical tensile measurement. Specifically, GO-ZnO coating on PLA substrate exhibited stability in aqueous food simulants for packaging application. GO-ZnO coating inhibited the infectious growth ofE. colibiofilm. GO-ZnO/PLA films had strong tensile strength and elastic modulus. As a result, the investigation of antibacterial GO-ZnO hydrogel and GO-ZnO coating on PLA film is fundamental for sustainable development of packaging and biomedical applications.

Revisiting oxidation and reduction reactions for synthesizing a three-dimensional hydrogel of reduced graphene oxide.

An improvement to Hummers' method involving a cascade-design graphite oxidation reaction is reported to optimize safety and efficiency in the production of graphite oxide (GrO) and graphene oxide (GO). Chemical reduction using highly alkaline ammonia solution is a novel approach to synthesizing reduced graphene oxide (RGO). In this original research, we revisit the oxidation and reduction reactions, providing significant findings regarding the synthetic pathway to obtain a bioinspired water-intercalated hydrogel of RGO nanosheets. Influential factors in the graphite oxidation reaction, typically the exothermic reaction temperature and hydrogen peroxide effect, are described. Furthermore, the chemical reaction of GO reduction using highly alkaline ammonia solution (pH 14) was investigated to produce hydrated RGO nanosheets assembled in a hydrogel structure (97% water). Three-dimensional assembly and water intercalation are key to preserve the non-stacking state of RGO nanosheets. Therefore, ultrasound transmission to aqueous channels in the macroscopic RGO hydrogel vibrated and dispersed the RGO nanosheets in water. Analytical results revealed the single-layer nanostructures, functional groups, optical band gaps, optimized C/O ratios, particle sizes and zeta potentials of GO and RGO nanosheets. The reversible self-assembly of RGO hydrogels is essential for many applications, such as RGO coatings and polymer/RGO nanocomposites. In a water purification application, the RGO hydrogel was dispersed in aqueous solution by simple agitation and showed a high capacity for organic dye adsorption. After the adsorption, the RGO/dye particles were easily removed by filtration through ordinary cellulose paper. The process of adsorption and filtration is effective and inexpensive for practical environmental remediation. In summary, a bioinspired structure of RGO hydrogel is conceptualized for prospective nanotechnology.

Effectiveness of photocatalysis of MMT-supported TiO2 and TiO2 nanotubes for rhodamine B degradation.

The aim of this paper is to synthesize montmorillonite/TiO2-nanoparticles (MMT/TiO2 and montmorillonite/TiO2-nanotubes (MMT/TiO2-NTs) photocatalysts through a simple wet agitation method based on TiO2 nanoparticles and MMT. They are likely to accumulate the effect of adsorption and photodegradation. Then, the photocatalysts are applied to degrade the rhodamine B in dye effluents. The structural characterizations of photocatalysts are investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and energy-dispersive X-ray spectroscopy (EDX). The photocatalytic activities and effectiveness of photocatalysts are evaluated through rhodamine B degradation at different concentrations under dark and UV-C irradiation conditions. The results show that the synthesized TiO2-NTs have an average tube diameter of 5 nm and a tube length at least about 110 nm, which are intercalated into MMT sheets in MMT/TiO2-NTs photocatalyst. Meanwhile, TiO2 nanoparticles are immobilized on the surface of MMT sheets in the MMT/TiO2 photocatalyst. The photocatalytic effectiveness of rhodamine B degradation of TiO2-NTs shows a significantly enhance compared to that of TiO2 nanoparticles. However, photocatalytic performance of MMT/TiO2-NTs is lower than that of MMT/TiO2. The degradation effectiveness of MMT/TiO2 photocatalyst reaches to 100% for 3 ppm and 90% at 10 ppm of rhodamine B, while these values are 97.5% and 85.5%, respectively, recorded for MMT/TiO2-NTs.