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In this work, experiments and modeling for the interactions between uranyl ion and GMZ bentonite in the presence of fulvic acid are presented. The results demonstrated that FA is strongly bound to GMZ bentonite, and these molecules have a very large effect on the U(VI) sorption. The results also demonstrated that U(VI) sorption to GMZ bentonite in the presence and absence of sorbed FA can be well predicted by combining SHM and DLM. According to the model calculations, the nature of the interactions between FA with U(VI) at GMZ bentonite surface is mainly surface complex. The first attempt to simulate clay interaction with humus by the SHM model. [ABSTRACT FROM AUTHOR]

In this work, experiments and modeling for the interactions between uranyl ion and TiO2 in the presence of fulvic acid are presented. The results demonstrated that FA is strongly bound to TiO2, and these molecules have a very large effect on the U(VI) sorption, and vice versa. The results also demonstrated that U(VI) sorption to TiO2 in the presence and absence of sorbed FA can be well predicted with the SCD model (surface and complex distribution). According to the model calculations, the nature of the interactions between FA with U(VI) at TiO2 surface is mainly surface complex and electrostatic potential. [ABSTRACT FROM AUTHOR]

Highlights: [•] Experiment data for the interactions between SA with Cu(II) at the surface of MWCNTs. [•] π–π Bonds sites perform quantitative modeling of adsorption by DLM model. [•] Cu(II) and SA sorption to MWCNTs can be well described with the DLM model. [•] The interactions with SA/Cu(II)/MWCNTs can be well predicted with the DLM model. [Copyright &y& Elsevier]

Abstract: Novel magnetic organo-bentonite-Fe3O4 poly(sodium acrylate) (OB-Fe3O4 PSA) superabsorbent nanocomposites were synthesized in aqueous solution through the copolymerization of partially neutralized acrylic acid (SA) on OB-Fe3O4 nanoparticle by using N,N′-methylenebisacrylamide as crosslinker and ammonium persulfate as initiator. This new superabsorbent was characterized by FTIR, TGA, FE-SEM and XRD. Its iron content and magnetic properties were studied by using inductively coupled plasma (ICP) and a vibrating sample magnetometer (VSM), respectively. The water retention test of OB-Fe3O4 PSA was also performed. The introduced OB-Fe3O4 could form a loose and coarse surface and improve the water absorbency of OB-Fe3O4 PSA superabsorbent. The effects of pH, ionic strength, and humic substances (HS) on the adsorption of Th(IV) were investigated in detail through batch experiments. The maximum adsorption capacity (Qmax ) of Th(IV) on OB-Fe3O4 PSA 3.6 superabsorbent at pH 3.0±0.05 and T=298K was about 6.55mmol/g, higher than any value previously reported. The thermodynamic parameters calculated from temperature-dependent adsorption isotherms suggested that Th(IV) adsorption on OB-Fe3O4 PSA superabsorbent was an endothermic and spontaneous process. Furthermore, OB-Fe3O4 PSA superabsorbent could be regenerated through the desorption of Th(IV) using 0.1mol/L HCl solution and the adsorption capacity was still higher than 3.6mmol/g after five consecutive adsorption–desorption processes. [Copyright &y& Elsevier]

The adsorption of Cu(II) on oxidized multi-walled carbon nanotubes (oMWCNTs) as a function of contact time, pH, ionic strength, temperature, and hydroxylated fullerene (C60(OH)n) and carboxylated fullerene (C60(C(COOH)2)n) were studied under ambient conditions using batch techniques. The results showed that the adsorption of Cu(II) had rapidly reached equilibrium and the kinetic process was well described by a pseudo-second-order rate model. Cu(II) adsorption on oMWCNTs was dependent on pH but independent of ionic strength. Compared with the Freundlich model, the Langmuir model was more suitable for analyzing the adsorption isotherms. The thermodynamic parameters calculated from temperature-dependent adsorption isotherms suggested that Cu(II) adsorption on oMWCNTs was spontaneous and endothermic. The effect of C60(OH)n on Cu(II) adsorption of oMWCNTs was not significant at low C60(OH)n concentration, whereas a negative effect was observed at higher concentration. The adsorption of Cu(II) on oMWCNTs was enhanced with increasing pH values at pH < 5, but decreased at pH ≥ 5. The presence of C60(C(COOH)2)n inhibited the adsorption of Cu(II) onto oMWCNTs at pH 4–6. The double sorption site model was applied to simulate the adsorption isotherms of Cu(II) in the presence of C60(OH)n and fitted the experimental data well. [ABSTRACT FROM AUTHOR]