RESUMO Neste trabalho, compósito Fe2O3/grafite foi preparado e usado como um catalisador em reação foto-Fenton para a descoloração de solução aquosa contendo o corante amaranto sob irradiação de luz visível. Amostras com diferentes teores de Fe2O3 suportados sobre grafite foram preparadas e caracterizadas por difração de raios-X (DRX), adsorção-dessorção de N2 e microscopia eletrônica de varredura (MEV). O aumento do teor de ferro nos compósitos resultou em uma superior área de superfície específica. Através da metodologia de superfície de respostas gerada a partir do Delineamento Composto Central Rotacional (DCCR), verificou-se uma eficiência máxima de descoloração da solução de corante de 93% nas condições experimentais ótimas de reação foto-Fenton (pH = 2,5, quantidade de catalisador = 0,35 g L-1 e razão molar H2O2/Ʃ elementos mineralizáveis: 4,7). Portanto, o compósito Fe2O3/grafite pode ser utilizado como um potencial catalisador foto-Fenton para a degradação do corante amaranto em efluentes líquidos.

ABSTRACT In this work, Fe2O3/graphite composite was prepared and used as a catalyst in photo-Fenton reaction for the decolorization of amaranth dye from aqueous solution under visible light irradiation. Samples with different Fe2O3 contents supported on graphite were prepared and characterized by X-ray diffraction (XRD), N2 adsorption-desorption and scanning electron microscopy (SEM). The increase of the iron content in the composites resulted in a superior specific surface area. The response surface methodology generated from the Rotational Central Composite Design (RCCD) showed a maximum efficiency in the decolorization of the dye solution of 93% under the optimal experimental conditions of photo-Fenton reaction (pH = 2.5, amount of catalyst = 0.35 g L-1 and molar ratio H2O2/Ʃ mineralizable compounds: 4.7). Therefore, the Fe2O3/graphite composite can be used as a potential photo-Fenton catalyst for the degradation of amaranth dye from liquid effluents.

In this work, cobalt ferrite (CoFe2O4) was synthesized by solvothermal route for application as a catalyst in the ozonation reaction for the decolorization and mineralization of melanoidin from aqueous solution. The structural properties of CoFe2O4 sample were investigated by X-ray diffraction (XRD), nitrogen adsorption-desorption isotherms, Fourier-transform infrared spectroscopy (FTIR), particle-size distribution, scanning electron microscopy (SEM) and X-ray dispersive energy spectroscopy (EDS). Single-phase CoFe2O4 particles with a predominantly mesoporous structure containing a high specific surface area were obtained. Results showed that the CoFe2O4-catalyzed ozonation reaction has higher activity for the decolorization and mineralization of melanoidin when compared with the ozonation reaction without the presence of catalyst. Therefore, this material can be very promising for the application in catalytic ozonation systems for the melanoidin removal from liquid effluents.

Nickel ferrite/multi-walled carbon nanotubes (NiFe2O4/MWCNTs) composite has been rapidly synthesized via microwave irradiation technique. The structural properties of the product was investigated by X-ray diffraction (XRD), N2 adsorption/desorption isotherms, thermogravimetric analysis (TGA), Raman spectroscopy and, scanning electron microscopy (SEM). Catalytic behavior of the composite material on the advanced photo-Fenton degradation of Amaranth dye was evaluated. The synthesis conditions employed on the microwave system were: temperature (235 °C), power (500 W), pressure (600 psi) and irradiation time (30 min). Characterization results showed the formation of hybrid material, containing a predominantly microporous structure, with surface area and total pore volume of 54 m2 g-1 and 0.2249 cm3 g-1, respectively. The composite exhibited higher catalytic activity compared to the pure NiFe2O4, reaching 100% of decolorization at 60 min of reaction, which can be attributed to a synergism between NiFe2O4 and MWCNTs. Therefore, NiFe2O4/MWCNTs composite can be used as a promising photo-Fenton catalyst to degrade Amaranth dye from aqueous solutions.

This study investigated the potential of Brazilian kaolin as a low-cost adsorbent for the removal of Malachite Green (MG) from colored effluents. The morphology, chemical structure and surface properties of the adsorbent were investigated by characterization techniques such as X-ray diffraction, N2 adsorption-desorption isotherms, Fourier transform infrared spectroscopy, X-ray fluorescence spectrometry, scanning electron microscopy, thermogravimetric analysis and particle size distribution. A possible technological application of raw kaolin is the MG removal from aqueous media, which was investigated using batch adsorption experiments. The adsorption kinetics was studied using the pseudo-first order, pseudo-second order and Elovich models. The adsorption isotherms were studied using the Langmuir, Freundlich and Sips models. The Elovich model was the more adequate to represent the adsorption kinetic, while the equilibrium was well represented by the Langmuir model. The maximum adsorption capacity, at pH of 6.3 and temperature of 25ºC, was 128 mg g-1, and this satisfactory result may be associated with some adsorbent properties. Therefore, the results revealed that raw kaolin can be utilized as a promising low-cost adsorbent to remove MG from colored effluents.

Mesoporous Fe2O3-supported ZSM-5 zeolites were prepared by carbon-templating and subsequently evaluated as photo-Fenton catalysts to degrade a dye used as a model heavy organic pollutant. The synthesis procedure of the mesoporous ZSM-5 zeolites was performed employing a nucleating gel and carbon particles as mesopores template. Thereafter, the precursor salt of the iron oxide (Fe2O3) was impregnated and then calcined to obtain the final catalyst. For comparison purposes, a conventional Fe2O3-supported ZSM-5 zeolite was also prepared. The results showed that the amount of intracrystalline mesopores formed in the ZSM-5 crystals was influenced by the amount of carbon added into the synthesis mixture. In comparison to the conventional prepared catalyst, the mesoporous Fe2O3/ZSM-5 ones showed an improved performance in the degradation of the target organic pollutant by the photo-Fenton reaction, which was attributed to the improvement of their textural properties as consequence of the mesopores generation.

In this work was investigated the influence of pH on the synthesis of struvite using cola beverage waste as source of phosphorus. The process was operated in a batch reactor. The reaction time was 20 minutes, and the chemicals MgCl2.6H2O and NH4Cl were used in the experiment, with a molar ratio of Mg+2:NH4+:PO4(3-) = 1:1:1. The products were characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), surface area (BET), thermogravimetric analysis (TGA) and infra-red (IR). From the results was verified the formation of a crystalline phase at pH 9.5, with a surface area of 6.59 m² g-1 and a particle size of about 0.25 µm.

Sodium silicate is used as raw material for several purposes: silica gel production, preparation of catalysts, inks, load for medicines, concrete hardening accelerator, component of detergents and soaps, refractory constituent and deflocculant in clay slurries. In this work sodium silicate was produced by reacting rice hull ash (RHA) and aqueous sodium hydroxide, in open and closed reaction systems. The studied process variables were time, temperature of reaction and composition of the reaction mixture (expressed in terms of molar ratios NaOH/SiO2 and H2O/SiO2). About 90% silica conversion contained in the RHA into sodium silicate was achieved in closed system at 200 °C. The results showed that sodium silicate production from RHA can generate aggregate value to this residue.

Currently, the accumulation of rice husk is a serious environmental problem. The burning of rice husk generates a considerable volume of ash, that falls to the ground and gets into the air and the rivers, causing a disequilibrium in the ecosystem. This motived research into solutions that aim to exploit the husks for energy generation and the ashes for developing diverse technological products. This work presents the possibilities of using rice husks and their ashes after burning.