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A magnetic geopolymer was prepared from the silica and metakaolin under presence of zero–valent iron (ZVI). The magnetic geopolymer was characterized by Fourier–Transform Infrared spectroscopy, X-ray diffraction, N2 adsorption/desorption isotherms, scanning electron microscopy, and vibrating sample magnetometer. The geopolymer was employed as adsorbent of Acid Red 97 dye. The results showed that the magnetic geopolymer have mesoporous structure and sufficient magnetization to be removed by a magnetic field from aqueous solution. Both the pseudo–first and pseudo–second order models satisfactorily described the adsorption kinetics, and the isotherms were properly adjusted by the Henry's model. High adsorptive capacity of dye (1814 mg g−1) was obtained, and the geopolymer can be used for five times with the same initial adsorption capacity. An efficient adsorbent was developed from low cost materials. This adsorbent presented extremely high adsorption capacity and can be easily separated from the treated liquid effluent. [ABSTRACT FROM AUTHOR]

• Quaternary adsorption of Cu2+, Co2+, Ni2+ and Ag+ ions was investigated. • Development of a new quaternary adsorption model. • Adsorption of Cu2+, Co2+ and Ni2+ ions was endothermic, while the Ag+ adsorption was exothermic. • Ag+ adsorption was reduced from single-compound to quaternary system. Quaternary adsorption of Cu2+, Co2+, Ni2+ and Ag+ ions on an adsorbent obtained from the alkaline fusion of wastewater treatment sludge was investigated. Adsorption tests in both single-compound and quaternary systems were carried out and the analysis of adsorption mechanism was done by the application of a new quaternary model. This model was developed from a general methodology based on the application of grand canonical ensemble in statistical physics. This adsorbent was characterized by different analytical techniques. Experimental data showed that the adsorption of Cu2+, Co2+and Ni2+ ions was endothermic, while the Ag+ adsorption was exothermic. Ag+ adsorption was significantly reduced from single-compound to quaternary system due to the competitive effect caused by the other divalent ions, while the adsorption capacities of Cu2+, Co2+ and Ni2+ were not significantly affected in the multicomponent solution. A significant competitive effect of Cu2+, Co2+ and Ni2+ ions on the adsorption of Ag+ ions occurred. Modelling analysis showed that the adsorption of Cu2+, Co2+ and Ni2+ ions was a multi-ionic process at all tested temperatures, while the adsorption of Ag+ was a multi-ionic process only at low temperatures (298 and 308 K). Finally, the statistical physics model confirmed that the adsorption energies corresponded to physical interactions forces and the water molecule adsorption played a relevant role during the removal of these trace metals. [ABSTRACT FROM AUTHOR]

• Two new adsorbents were prepared for dye adsorption from aqueous solution. • Statistical physics modeling was performed to characterize dye adsorption mechanism. • Physical interactions were involved in the endothermic dye adsorption. • Dye adsorption capacities ranged from 281 to 632 mg/g. Activated carbons were prepared from ashitaba waste and a walnut shell to study the adsorption mechanism of congo red and methylene blue dyes in aqueous solution. These adsorbents were characterized via XRD, FTIR and SEM techniques and the dye adsorption isotherms at three temperatures were quantified. A statistical physics model was applied to interpret the adsorption mechanism of tested dyes and adsorbents. Modeling results showed that these dyes were practically separated in the solution leading to an absence of the aggregation process. Adsorption orientations of dye molecules on the adsorbents changed depending on the temperature and nature of systems. The adsorption capacity of ashitaba waste activated carbon for the removal of congo red was significant thus indicating strong interactions between this dye and tested adsorbent. Calculated adsorption energy varied from 7.25 to 20.43 kJ/mol and they showed that the adsorption of both adsorbates occurred via physical interactions at different temperatures where the removal process was endothermic. [ABSTRACT FROM AUTHOR]