RESUMO

Selective photocatalytic oxidation of benzyl alcohol to benzaldehyde and reduction of nitrobenzene to aniline reactions are investigated by using SiO2@TiO2 spheres produced in a simple route using chitosan as a template. The spheres are predominantly macroporous and, the XRD points out an amorphous crystallographic profile suggesting the uniform distribution of TiO2. Under low-power lighting for 4 hours, the conversions achieved was of the order of 49% and 99% for benzyl alcohol and nitrobenzene, respectively, with selectivity to benzaldehyde and aniline of 99% in both reactions. The study also follows the effects of the solvent and the presence of O2.

Assuntos

Álcool Benzílico , Dióxido de Silício , Benzaldeídos , Nitrobenzenos/química , Compostos de Anilina

RESUMO

This study presents a new procedure for the determination of trace levels of copper(II) in an aqueous matrix, through flow injection (FI) on-line preconcentration with a minicolumn packed with silica gel modified with 3(1-imidazolyl)propyl groups. After the preconcentration stage, the analyte was eluted with a HNO(3) solution and determined by flame atomic absorption spectrometry (FAAS). The measurements of the analytical signals were carried out as peak area and peak height with the objective of evaluating the most appropriate absorption measurement for the proposed method. Four procedures to calculate the experimental enrichment factor (EF) were also studied. For a preconcentration time of 90s the enrichment factors found in this study varied between 19.5-25.8 and 36.2-42.2 for peak area and peak height, respectively. The precision of the proposed method was calculated for a solution containing 20mugl(-1) of Cu(II), when 11.2ml of solution was preconcentrated (n=7), and their respective relative standard deviation (R.S.D.) values were 1.2 and 1.4% for peak area and peak height, respectively. The detection limits obtained were 0.4 and 0.2mugl(-1) of Cu(II) for peak area and peak height, respectively, with a preconcentration time of 90s. The on-line preconcentration system accuracy was evaluated through a recovery test on the aqueous samples and analysis of a certified material.