The ion exchange of Na for Cr/K, Cr/Mg and Cr/Ca in Y and X zeolites was studied using breakthrough curves. It was observed that Cr3+ ions were able to remove some competitive ions that had already been exchanged at the zeolitic sites, producing a sequential ion exchange. Some mass transfer parameters such as length of unused bed, overall mass transfer coefficient, operational ratio and dimensionless variance were studied. Chromium uptake was influenced much more by the competing ion in the NaX zeolite columns. The dimensionless variance indicated that Cr/K solution produced a greater axial dispersion than the Cr/Mg and Cr/Ca systems, probably due to some interaction between Cr3+ and K+ ions. The order of dynamic selectivity, provided by the cation uptake, was Cr3+ > Ca2+, Cr3+ > Mg2+ and Cr3+ > K+ for NaY zeolite and Ca2+ ~Cr3+, Mg2+ > Cr3+ and Cr3+ > K+ for NaX zeolite. Due to the more favorable mass transfer parameters and higher affinity for Cr3+, it was concluded that NaY zeolite was more efficient at chromium uptake in competitive systems.

This work aimed to determine the maximum content of cobalt that can be incorporated by ion exchange in zeolites H-USY, H-Beta, H-Mordenite, and H-ZSM-5. To reach this goal, batch isotherms at 75ºC were constructed after addition of zeolite samples in flasks filled with cobalt nitrate solution. The equilibrium data were fitted to Langmuir, Freundlich, and Tóth adsorption isotherm models. Langmuir was the best model for zeolites H-Beta, H-Mordenite, and H-ZSM-5, whereas experimental data for H-USY were better fitted to the Freundlich isotherm model. From the isotherms, it was possible to determine the maximum cobalt exchange level (q max) that can be incorporated in each zeolite through ion exchange. In this sense, H-USY presented the highest q max value (2.40 meq/g zeol), while H-ZSM-5 showed the lowest one (0.64 meq/g zeol). These results also show the influence of the zeolite framework related to the channel system, pore opening, presence of cavities and secondary porosity and SiO2/Al2O3 ratio (SAR) on the maximum capacity and behavior of cobalt ion exchange in protonic zeolites.

Abstract In this study the influence of the volumetric flow rate and feed concentration was investigated for the adsorption of the reactive dye Blue 5G. Experiments were carried out in a bed packed with retorted shale, at 30 ºC. The ranges investigated were flow rate 2 -10 mL/min and the feed concentration 13-105 mg/L. Mathematical models were used to represent the dynamic sorption. The double resistance model considers the effects of the axial dispersion and the mass transfer resistance of the external film and inside the particles. As a result, the mass transfer coefficient of the external film and the internal mass transfer coefficient were estimated. The Thomas model was used to simulate the experimental data. In this model the fitted parameter was the adsorption kinetic constant. The first model provided an acceptable representation of the dynamic uptake of the reactive dye Blue 5G.

A aplicação de argilas para adsorção de metais pesados presentes em efluentes tem sido objeto de estudo em muitas pesquisas em virtude das inúmeras vantagens técnicas e econômicas. Este trabalho teve como objetivo obtenção de isotermas de adsorção de níquel e zinco em coluna de leito fixo utilizando como adsorvente argila bentonita calcinada a 500 ºC. Os experimentos para remoção de níquel e zinco foram conduzidos à temperatura ambiente (20 ºC - 25 ºC), pH da alimentação ajustado em 4,5, massa de argila calcinada de 15,5 g, com diâmetro médio de 0,855 mm, vazão de alimentação de 4 mL/min e concentração da solução de metal variando entre 0,5 meq/L a 4 meq/L. Os modelos de isoterma de Langmuir, Freundlich, Langmuir-Freundlich, Radke-Prausnitz, Redlich-Peterson, Sips e Toth foram ajustados aos dados de equilíbrio, sendo que o modelo de Langmuir apresentou melhor ajuste às concentrações de Ni2+ e Zn2+ adsorvido.

The adsorption of reactive turquoise blue QG dye on commercial activated carbon was investigated in a batch reactor to obtain isotherm and kinetic data under different experimental conditions. The adsorbent was characterized by a FTIR method to analyze surface area and pH PZC and to identify functional groups. Experiments were conducted to obtain equilibrium data at 30°C, with the pH effect being assayed in the range of 2 to 8. Experiments were then carried out under the optimal pH condition for dye removal to obtain equilibrium data at 30°C, 45°C and 60°C. Adsorption isotherm models were used to correlate the equilibrium data. Maximum dye removal capacity was observed at a pH of 2 and temperature of 30°C. The kinetic experiments were carried out at a pH of 2 and at three different temperatures: 30°C, 45°C and 60°C. Pseudo-second-order models were used to describe the kinetics of dye adsorption.