Oxidic Substrate with Variable Charge Surface Chemically Modified for Copper Ion Adsorption from Aqueous Solutions

The presence of toxic elements in drinking water poses important risks to human health. Among the diverse methodologies available to remove these elements from water, adsorption methods are among the most effective: however, many adsorbent materials are either costly, not widely available, or difficult to handle. This work focuses on the application of a new natural geologic material, named &ldquo:V&rdquo: material, to prepare an adsorbent substrate applied to water treatment, using its adsorption properties to remove metallic species from aqueous media. The geologic material is a thermally and mechanically resistant material, composed basically of quartz, iron and aluminum oxides, with amphoteric properties. A granular medium or substrate was prepared via thermal treatment using three granulometric fractions of the material: the smaller fraction, less than 250 &mu:m, named the fine fraction, VFF: from 250 &mu:m to 425 &mu:m, named the medium fraction, VMF: and from 425 &mu:m to 1200 &mu:m, named the gross fraction, VGF. The experiments were carried out on both alkaline-treated and non-treated substrates, named activated and non-activated substrates, respectively. The BET and external surface, as well as the pore volume, increased significantly after the calcination process. The adsorption isotherms pointed to a strong interaction between metallic ions and activated substrates, in contrast to the non-activated substrate, which showed much less affinity. This type of isotherm is associated with specific adsorption, where the adsorption occurs chemically between Cu2+ ions and the substrate surface, basically composed of amphoteric metallic oxides. The adsorption data fit fairly well to the Freundlich and Langmuir models, where the K values are higher for activated substrates. According to the Freundlich K values, the copper adsorptions on the activated substrates were higher: 5.0395, 3.9814 and 4.2165 mg/g, compared with 0.3622, 1.8843 and 0.4544 mg/g on non-activated substrates. The pH measurements showed the production of 0.56 and 0.10 &mu:mol H+ during the adsorption reaction on the activated substrate, following the theoretical model for the chemisorption of transitional metals on amphoteric oxides. These results show the potential applicability of this kind of substrate in retaining transitional metals from polluted drinkable water at low cost. It is environmentally friendly, non-toxic, and available for rural media and mining-impacted regions.