RESUMO
Here we propose an innovative photocatalytic hybrid system for the reduction of hexavalent chromium (Cr(VI)) from aqueous solutions. The hybrid system was composed of titanium dioxide (TiO2) immobilized in the micro-voids of asymmetric alumina hollow fibers and of the green algae Chlorella vulgaris coated on the outer sponge-like layer of the fiber. The photoreduction of Cr(VI) was systematically studied in different systems: single systems with TiO2 or algae; the synergistic system of algae combined with TiO2; and the proposed hybrid system composed of TiO2 and algae supported in ceramic hollow fibers. Morphological and energy dispersive spectroscopy analyses showed that TiO2 and the algae were properly supported in the substrate (alumina hollow fibers). For an initial Cr(VI) concentration of 10 mg L-1 and dosages of 1 g L-1 of TiO2 and algae, the hybrid system resulted in total Cr(VI) reduction after 16 h of process. Additionally, the efficiency of the hybrid system for Cr(VI) reduction was reduced in only 9% after 5 cycles of reuse and in 42% after 10 cycles of reuse. Thus, micro-structured ceramic hollow fibers impregnated with TiO2 and decorated with the green algae C. vulgaris was efficient for Cr(VI) reductions.
Assuntos
Cerâmica/química , Chlorella vulgaris/crescimento & desenvolvimento , Cromo/análise , Fibras Minerais , Titânio/química , Poluentes Químicos da Água/análise , Purificação da Água/métodos , Catálise , Cromo/efeitos da radiação , Cinética , Luz , Oxirredução , Fotoquímica , Poluentes Químicos da Água/efeitos da radiaçãoRESUMO
The plasma electrolytic oxidation (PEO) technique was used to prepare photocatalytic S-TiO2 coatings on Ti sheets; the incorporation of the S ions was possible from the electrolyte for modifying the structural and optics characteristics of the material. In this work, substrates of Ti (ASME SB-265 of 20 × 20 × 1 mm) were used in a PEO process in 10 min, using constant voltage pulses of 340 V with frequency of 1 kHz and duty cycles of 10% and of 30%. Solutions with H2SO4 (0.1 M) and CH4N2S (52 and 79 mM) were used as electrolytes. X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy (EDS) were utilized to analyze the surface morphology, crystalline phase, and chemical composition of the samples. According to the results, the catalyst coatings had microporous structure and contained anatase-rutile TiO2 nanocrystalline mixture, until 73.2% rutile and 26.8% anatase in the samples grown with 30% duty cycle and the lowest concentration of CH4N2S. From the EDS measurements, the incorporation of sulfur ions to the coatings was 0.08 wt%. 99.5% reduction efficiency of Cr(VI)-EDTA with sunlight was observed after 2 h; it was determined by diphenyl carbazide spectrophotometric method. These coatings have potential for effective sunlight heterogeneous photoreduction of this toxic, cumulative, and non-biodegradable heavy metal that contaminates the soil and water and is a serious risk to sustainability, ecosystems, and human health.
Assuntos
Poluentes Atmosféricos/análise , Cromo/análise , Ácido Edético/química , Enxofre/química , Luz Solar , Titânio/química , Poluentes Atmosféricos/efeitos da radiação , Catálise , Cromo/efeitos da radiação , Eletrólitos/química , Oxirredução , Gases em Plasma/química , Porosidade , Propriedades de SuperfícieRESUMO
The feasibility of the photobleaching of a leather acid dye, acid red 151, simultaneously to degradation of anionic surfactant, Tamol, and reduction of Cr(VI) to the less toxic Cr(III) was investigated by photoelectrocatalytic oxidation. The best experimental conditions were found to be pH 2.0 and 0.1 mol L(-1) sodium sulfate when the nanoporous Ti/TiO2 photo anode was biased at +1.0 V and submitted to UV-irradiation. The photoelectrocatalytic oxidation promotes 100% discoloration, reducing around 98-100% of Cr(VI) and achieving an abatement of 95% of the original total organic carbon. The effect of pH, the applied potential, the Cr(VI) concentration and the complexation reaction between Cr(VI) and acid red dye were evaluated as to their effect on the kinetics of the reaction.