Silver nanoparticles effect on Artemia salina and Allium cepa organisms: influence of test dilution solutions on toxicity and particles aggregation.

The objective of this study was to evaluate the effects of AgNPs on Artemia salina and Allium cepa, evaluating the influence of the dilution solutions on the particle behavior. The AgNPs were synthesized by chemical reduction of AgNO3 (3 and 5 mmol L-1) with sodium borohydride and stabilized with PVA (polyvinyl alcohol) and CMC (sodium carboxymethyl cellulose). The toxicity of AgNPs was evaluated in Artemia salina (mortality) using Meyer's solution as a diluent and in Allium cepa (chromosomal aberrations) using reconstituted hard water. AgNPs showed characteristic molecular absorption bands. Particles with CMC presented hydrodynamic radius between 4 and 102 nm and with PVA between 7 and 46 nm. The studied dispersions were toxic to A. salina species. Meyer's solution, used as dilution water in the test, caused precipitation of Ag+ and also caused changes in CMC-stabilized AgNPs, changing the shape of the nanoparticles by depositing precipitates on their surface. These changes make the results of toxicity difficult to interpret. AgNPs stabilized with PVA remained unchanged. AgNPs affected cell division and caused the appearance of chromosomal aberrations on A. cepa. Higher numbers of chromosomal aberrations occurred in dispersions with smaller particle diameters (AgNPs3-PVA and AgNPs5-PVA, without dilution). In the studied conditions the dispersions were toxic to the tested organisms, the concentrations of precursors and the type of stabilizer used influenced the particle size and toxicity. In the test with A. cepa, the reconstituted hard water did not cause changes in the dispersions of AgNPs, whereas for A. salina the Meyer solution promoted aggregation of the particles and precipitation, in the dispersions stabilized with CMC, thus changing the samples.

SPME fiber coated by arrayed ZNRs for sampling and concentration of polar residual solvents for further analysis using GC FID.

In this work, fused silica coated by arrayed ZNRs were successfully applied as a sorbent for analysis of polar residual solvents in pantoprazole feedstocks. ZnO nanoparticles were produced and deposited on a fused silica surface applying the dip coating technique and hydrothermal growth to synthesize the arrayed nanorods. The ZNRs array fiber coating was characterized by SEM, EDS, XRD, and TGA. The manufactured SPME fiber was coupled to a glass syringe of 10 µL and applied for the sampling of acetone, n-butanol, dichloromethane, ethyl acetate and methanol for further analysis using GC FID. Optimum operating conditions were determined for the incubation temperature (70 °C), incubation time (15 min), extraction time (120 s), and desorption time (0.6 min). Employing the optimum conditions, the proposed method resulted in a good linearity (> 0.997) and precision (< 7.1%) for the evaluated analytes. Recovery tests were also performed on three levels (below, equal to and above the ICH specification limit for residual solvents in pharmaceutical products). Recoveries ranging from 96% to 107% were obtained. Comparison between the reference method and developed method shows errors smaller than 4%.

Adsorption of reactive blue BF-5G dye by soybean hulls: kinetics, equilibrium and influencing factors.

The textile industry is known for the high use of chemicals, such as dyes, and large volumes of effluent that contaminate waters, a fact that has encouraged research and improved treatment techniques. In this study, we used unprocessed soybean hulls for the removal of reactive blue BF-5G dye. The point of zero charge of soybean hulls was 6.76. Regarding the speed of agitation in the adsorption process, the resistance to mass transfer that occurs in the boundary layer was eliminated at 100 rpm. Kinetics showed an experimental amount of dye adsorbed at equilibrium of 57.473 mg g(-1) obtained under the following conditions: dye initial concentration = 400 mg L(-1); diameter of particle = 0.725 mm; dosage = 6 g L(-1); pH 2; 100 rpm; temperature = 30 °C; and duration of 24 hours. The pseudo-second order best showed the dye removal kinetics. The adsorption isotherms performed at different temperatures (20, 30, 40 and 50 °C) showed little variation in the concentration range assessed, being properly adjusted by the Langmuir isotherm model. The maximum capacity of dye adsorption was 72.427 mg g(-1) at 30 °C. Since soybean hull is a low-cost industrial byproduct, it proved to be a potential adsorbent for the removal of the textile dye assessed.

ZnO-coated glass fibers for the analysis of trihalomethanes by headspace-solid phase microextraction-gas chromatography.

Li(2)O-ZrO(2)-BaO-SiO(2) glass fibers were produced and their surfaces were coated with zinc oxide. The fibers' surface morphology was examined by scanning electron microscopy and the zinc oxide layer was characterized by mapping the K(α) and L(α) lines of zinc by energy dispersive X-ray spectroscopy. The results indicated that a homogeneous and porous layer of ZnO was formed on the fibers' surface. This layer was subjected to a simultaneous determination of trihalomethanes using headspace-solid phase microextraction-gas chromatography. The study was conducted after evaluating the ideal time of incubation (15 min), extraction (15 min) and desorption (10 min), as well as the effect of the addition of salt (15%, m/v) on the analytical response. A good linear dynamic range was observed individually for trihalomethanes aqueous solutions containing 20 µg L(-1) and 500 µg L(-1) of trichloromethane, 15 µg L(-1) and 250 µg L(-1) of dichlorobromomethane and dibromochloromethane and 10 µg L(-1) and 100 µg L(-1) of tribromomethane, with all the compounds showing correlation coefficients higher than 0.9900.