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.

The present work deals with the design and construction of an equipment for muti-cell accelerated stability test measurements (AST) of dimensionally stable anodes (DSA). The equipment was built using only components that were available in the laboratory. Measurements of three electrochemical cells can be performed using the developed software. The acquisition time interval and the cut-off potencial can be set by the user. Experimental data for RuO2 electrodes obtained with the built equipment are in agreement with the literature.