RESUMO Vários minerais e resíduos industriais têm sido estudados para uso como adsorvente, entre eles a lama vermelha e a anidrita. A lama vermelha é um resíduo insolúvel gerado em grande quantidade durante o processamento da bauxita. A anidrita é um sulfato de cálcio (CaSO4) cristalizado sob a forma rômbica e usada como matéria-prima na indústria. Nesta investigação, a capacidade de adsorção de Cd2+, Ni2+ e Zn2+ pela anidrita e pela lama vermelha foi avaliada usando isotermas de adsorção de Langmuir e Freundlich. Os materiais empregados apresentaram adsorção ≥75±1% para todos os metais em soluções aquosas com concentração de 0,5 mmol.25 mL-1. As isotermas baseadas no modelo de Langmuir foram as mais apropriadas para descrever o fenômeno de remoção de Cd2+, Ni2+ e Zn2+ para a anidrita e a lama vermelha, com valores de capacidade máxima de adsorção de 0,47 e 0,51 mmol.g-1 para o Cd2+, 1,18 e 1,56 mmol.g-1 para o Ni2+ e 0,84 e 1,47 mmol.g-1 para o Zn2+, respectivamente. Esses valores foram superiores a outros valores exibidos por materiais empregados como adsorventes descritos em estudos prévios.

ABSTRACT Various minerals and industrial waste have been studied for use as an adsorbent, in particular the anhydrite and the red mud. The red mud is an insoluble residue that is generated in large quantities during the processing of bauxite. The anhydrite is a calcium sulfate (CaSO4), crystallized as a rhombic way, and used as raw material in the industry. In this study, the Cd2+, Ni2+ and Zn2+adsorption capacity by anhydrite and by red mud was evaluated using adsorption isotherms obtained by the Langmuir and Freundlich models. The materials used showed adsorption ≥75±1% for all metals in aqueous solutions with a concentration of 0.5 mmol.25 mL-1. The Langmuir isotherm was more appropriate to describe the phenomenon of Cd2+, Ni2+ and Zn2+ removal, with highest adsorption capacity at 0.47 and 0.51 mmol.g-1 for Cd2+, 1.18 and 1.56 mmol.g-1 for Ni2+, and 0.84 and 1.47 mmol.g-1 for Zn2+, respectively. These values were higher than those ones obtained for other materials described in previous studies.

In this paper, we propose the production of ceramic protective thin films by plasma electrolytic oxidation using red mud-containing electrolytes. The treatments were performed through the application of pulsed voltage (600 V, 200 Hz) during 300 seconds to aluminum samples immersed in electrolytic solutions with 5 g of red mud per liter of distilled water. The coatings were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray energy dispersive spectroscopy (EDS) and contact angle and surface energy measurements. The final current density during the experiments was 0.05 A/cm² and films as thick as 9.0 µm have been obtained. XRD patterns have clearly shown the incorporation of species from the red mud on the coating.

During the extraction of aluminum from bauxite, a waste of oxides containing traces of heavy metals in a highly alkaline matrix, called Red Mud (RM), is produced. In this study RM is characterized and the feasibility of using it as a precursor for the production of thin films by Plasma Sputtering and by Plasma Immersion Ion Implantation and Deposition (PIIID) is demonstrated. The chemical structure and composition, surface morphology, topography, and wettability of the films prepared using such methodologies were investigated. The films consist mainly of the elements aluminum, silicon, iron and carbon. Infrared spectroscopic analyses reveal the presence of C=O, C-H2, Fe(OH), Al-O and Si-C functionalities. RF Sputtering produced films with smoother surfaces, whereas PIIID produced granular surface structures. Surface contact angle measurements showed that despite the presence of oxides and hydroxides, the films are hydrophobic, thus exhibiting an interesting link between the physical and thermodynamical properties.

Adsorption of Reactive Blue 19 dye onto activated red mud was investigated. Red mud was treated with hydrogen peroxide (LVQ) and heated at both 400 ºC (LVQ400) and 500 ºC (LVQ500). These samples were characterized by pH, specific surface area, point of zero charge and mineralogical composition. Adsorption was found to be significantly dependent on solution pH, with acidic conditions proving to be the most favorable. The adsorption followed pseudo-second-order kinetics. The Langmuir isotherm was the most appropriate to describe the phenomenon of dye removal using LVQ, LVQ400 and LVQ500, with maximum adsorption capacity of 384.62, 357.14 and 454.54 mg g-1, respectively.

Two sampling points were chosen and forty samples were collected between January and December 2006 at Alto Sorocaba basin. The rainwater pH varied from 5.46 to 6.36 (Ibiúna) and 5.26 to 6.81 (Itupararanga), being Ca2+ the main ion responsible for controlling the rainwater pH. The ionic concentrations decreased in the following order: Ca2 +>Na+> Mg2+>K+ for cations and SO4(2-)>HCO3->NO 3->Cl- >PO4(3-) for anions. The annual atmospheric deposition appeared to be controlled mostly by following sources: mining activities and cement factories (Ca2+ and HCO3-), natural soil dust (Na+, Mg2+ and HCO3-), fossil fuel burning (SO4(2-)) and agriculture activities (K+, NO3- and PO4(3-)).

In this work commercial filters papers were organomodified with tetraethylorthosilicate (TEOS) and 3-aminopropyltriethoxysilane (3-APTS), aiming at the development of a new analytical procedure for in-situ speciation of labile and inert metal species in aquatic systems. Parameters that exert influence on the metal lability such as pH, chelating time, concentration and characteristics of the organic matter were studied in the laboratory using tests for metal recuperation. The results showed slower kinetics for Cu ion than for Ni, Mn and Cd in the absence of aquatic humic substances (AHS). The relative lability observed for complexed metals in aquatic humic substances using organomodified filter papers was Cu>>Cd>Ni>Mn. The pH values, structural characteristics and concentration of AHS exert strong influence on the lability of the metals. The results obtained showed that the utilization of organomodified filter papers can be an interesting and promising alternative for in situ characterization of metal lability in aquatic systems.