In this work, cellulose-based composite biofilms doped with silver nanoparticles (AgNPs) have been produced by eco-friendly process. The AgNPs were synthesized from Ilex paraguariensis with an average size of 45 nm, a characteristic plasmon band at 450 nm and zeta potential of -23 mV. The biofilm has been synthesized by casting method, using different volumes of AgNPs suspension with glycerol plasticizing agent (T6-T10) or not (T1-T5). The AgNPs were successfully incorporated into the biofilms, which was confirmed by scanning electron microscopy. The mechanical and optical structural and the antimicrobial properties of the biofilms have been determined. In the presence of AgNPs, the mechanical properties, thermal stability and water vapor barrier of the biofilms have not been altered. However, the addition of glycerol decreased the tensile strength and the modulus of elasticity, in addition to increasing the elongation of the biofilms and the water vapor barrier. The biofilm T10 showed a transmittance of ca. 10%, with high potential to be used as a UV light blocker. Finally, the biofilms doped with AgNPs showed activity against the bacterium Pseudomonas fluorescens. Given the above, this work presented a new biofilm with activity against the bacterium Pseudomonus fluorescens obtained by eco-friendly process.

Phytochemical investigation of the inflorescences of Dictyoloma vandellianum A. Juss. (Rutaceae) has led to the isolation of a new A-seco-limonoid, named dictyolomol (1), along with a known quinolone alkaloid, casimiroine (2), previously isolated from the same species. The structures were established by spectroscopic analysis such as one- and two-dimensional NMR, IR, high-resolution mass spectrometry and chemical transformations. The isolated compounds (1 and 2) and O-acetyl derivative (1a) were evaluated for their cytotoxicity against MCF-7 and HeLa cancer cell lines. The results indicated that 1, 1a and 2 showed no significant cytotoxicity.

The cobalt nanoparticles (NPs-Co) were synthesized and applied in the removal of Cr(VI). The obtained nanomaterials presented magnetic properties and were characterized by the techniques of Transmission Electron Microscopy and X-ray diffraction. The NPs-Co, with a diameter of less than 50 nm, had a composition based on metallic cobalt and cobalt oxide. The NPs-Co were applied in the removal of Cr(VI) being evaluated different parameters such as time of equilibrium, initial pH, dose of NPs-Co, concentration of Cr(VI), and system temperature. The removal of Cr(VI) was favored at lower pH values, being about 100% at pH 2.0. With the increase of Cr(VI) concentration from 40.0 to 300.0 mg L-1 the removal decreased from 80 to 15%. The NPs-Co dose promoted an increase in removal reaching 90% at a dose of 1.0 g L-1. The removal process was spontaneous and endothermic, and the Langmuir isotherm model fit better to experimental data. The maximum removal capacity was approximately 70.0 mg g-1. The removal kinetics followed the pseudo-second order model. The mechanism of Cr(VI) removal occurred through adsorption by electrostatic interactions between CrO42- anion and Co-NPs, followed by reduction of Cr(VI) to Cr(III) and, lastly, co-precipitation of Cr(III) as Cr(OH)3 on the NPs-Co.

ABSTRACT Kinetic studies of sulfentrazone herbicide dechlorination by Fe/Ni nanoparticles were performed in the presence of different electrolytes such as: Cl-, SO42-, NO3-, Cu2+, Na+ and Zn2+. In the presence of Cl- and SO42- the reaction occurred efficiently, reaching approximately 100% of dechlorination after 30 minutes of reaction. In the presence of NO3- and Cu2+ ions the sulfentrazone dechlorination was significantly inhibited, because these ions tend to compete with the substrate for the electrons donated by Fe0. In the presence of Na+ ions, the dechlorination efficiency remained approximately 100%, however, this electrolyte provided an increase on the reaction rate, due to the increase of the ionic strength in the system. The Zn2+ ions has no influence on the dechlorination efficiency, but the reaction rate was reduced due to the formation of a protective layer formed by the sorption of Zn2+ ions on the surface of the nanoparticles.

The removal of the beta-lactam antibiotics (ceftriaxone and cefadroxil) through zero-valent copper nanoparticle (nZVC) was studied in this work. Excellent removal degrees (> 85%) were obtained for both analytes in only 20 min of reaction. Studies were performed in both oxic and anoxic conditions, and in the presence of t-butyl alcohol (TBA), an inhibitor of radicals. The results did not show significant changes. Therefore, the hydroxyl radicals are not the main species responsible for the removal. Total organic carbon cefadroxil analysis indicated a removal of 57% after 180 min of reaction. Studies involving Cu+ indicated that probably these are the principal species responsible for the removal of antibiotics. Kinetic studies have shown that two-phase reaction occurred in the antibiotics removal process and both phases followed pseudo-first order kinetic model. The first mechanism is related to the antibiotics degradation by Cu+ species and the second mechanism is related to the antibiotics adsorption by hydroxides/oxides of Cu2+ species.