Carbon dots (C-dots) possess the attractive properties of high stability, low toxicity, good water solubility, simple synthetic routes as well as size and excitation-dependent photoluminescence (PL).The aim of this work was to synthesize photoluminescent C-dots by hydrothermal method using acerola fruit (Malpighiaemarginata) as a row material, since this fruit contains large number of organic molecules. Studies about the optimal synthesis conditions were performed, where these organic molecules were converted into C-dots by hydrothermal carbonization at 180 ºC for 18 h. The C-dots exhibited a green emission light at 459 nm when excited under UV-light ( λ ex= 370 nm). These nanomaterials were also successfully used to prepare C-dots/poly (vinyl alcohol) luminescent composites (C-dots/PVA). Both C-dots and C-dots/PVA composite films were investigated by using colorimetric visual sensor for Fe3+ metal ions detection. The results show that the prepared C-dots and C-dots/poly presented strong green emission light. The emission spectra of above materials were quenched in the presence of Fe3+ ions. Thus, highly specific “turn off” fluorescence sensing of Fe3+ was achieved using fluorescent C-dots. Regarding, this work describe that the polymeric films as sensors of metallic ions in aqueous solution appears as a new perspectives to design new composite materials.

A new δ-FeOOH supported nano-Au catalyst was prepared by a facile method using HAuCl4 as the gold source and NaBH4 as the reducing agent. The samples (denoted as AuNPs/FeOOH) were characterized by means of X-ray diffraction (XRD), UV-vis and infrared spectroscopies and scanning electron microscope (SEM). The obtained characterization data confirmed the formation of Au nanoparticles on the δ-FeOOH matrix surface. SEM observations showed that Au nanoparticles have a spherical morphology and good dispersion with a narrow size distribution on the surface of iron (III) oxyhydroxide. The catalyst exhibits significantly high catalytic activity for hydrogenation of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) at room temperature. The high performance obtained can be attributed to the specific characteristics of the nanostructure of the catalyst of nano-Au deposited on the external surface of δ-FeOOH, including plenty of oxygen-containing groups of δ-FeOOH for anchoring AuNPs. Moreover, the catalytic activity increased when the AuNPs content in the δ-FeOOH support. The AuNPs-based δ-FeOOH hybrids are interesting catalysts for hydrogenation of nitrophenols to aminophenols.

Silver nanoparticles and zinc hydroxide-layered hybrid materials (AgNPs/ZHL) have been successfully developed as efficient catalysts for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) with sodium borohydride. A facile and rapid visible-light assisted green route was used for the deposition of silver nanoparticles (AgNPs) on the external surface of ZHL material. The resulting AgNPs/ZHL hybrids contained AgNPs with spherical morphology and uniform size distribution. Moreover, the AgNPs/ZHL compounds exhibited excellent catalytic performance (the reduction reaction was finished within 4 min) and reusability (three cycles) toward the reduction of 4-NP to 4-AP in presence of sodium borohydride. The reduction reaction obeyed the pseudo-first-order kinetics. The rate constants increased with the increase of amount of the AgNPs deposited into the hybrid materials. These results suggest that the as-prepared catalysts (AgNPs/ZHL) have great potential for heterogeneous catalytic applications.