Superparamagnetic Composites Based on Ionic Resin Beads/CaCO3 /Magnetite.

The preparation of superparamagnetic composites obtained by CaCO3 mineralization from supersaturate aqueous solutions is presented. The preparation was conducted in the presence of oleic acid stabilized magnetite nanoparticles as a water-based magnetic fluid and insoluble templates as gel-like cross-linked polymeric beads. The presence of the magnetic particles in the composites provides a facile way for external manipulation using a permanent magnet, thus allowing the separation and extraction of magnetically modified materials. Two ion exchangers based on divinylbenzene/ethyl acrylate/acrylonitrile cross-linked copolymer-a cation ion exchanger (CIE) and an amphoteric ion exchanger (AIE)-were used, as well as different addition orders of magnetite and CaCO3 crystals growth precursors. The morphology of the composites was investigated by SEM, the polymorphs content by X-ray diffraction, and the thermal stability by thermogravimetric analysis. Polymer, CaCO3 , and magnetite in the composite particles were shown to be present by energy dispersive X-ray (EDX), XPS, and TEM. The sorption capacity for CuII ions was tested, as compared to samples prepared without magnetite.

Valorization of Romanian silver fir tree bark (Abies alba Mill.) wastes as low-cost sorbent of Cu(II) ions from polluted waters.

Considering recycling as the first option in the hierarchy of sustainable waste management, and also the demand for efficient processes for wastewater treatment with reduced costs, the potential applicability of Romanian Abies alba bark, the main waste from the industrial processing of the wood of mature silver fir trees, as sorbent for Cu(II) has been studied in batch conditions. It was observed that the extent of Cu(II) sorption is strongly dependent on initial solution pH, sorbent dose, initial Cu(II) ion concentration, temperature and contact time. Equilibrium data fitted very well with both Langmuir and Freundlich isotherm models. The Langmuir maximum sorption capacity of Cu(II) ions on Abies alba bark waste was found to be 7.80 mg/g at 293 K. Kinetic studies showed a high affinity of the sorption experimental data to the pseudo-second order model. Gibbs free energy was spontaneous for all interactions and the sorption process exhibited endothermic enthalpy value. The waste of Abies alba bark was successfully used for the sorption removal of Cu(II) ions from industrial electroplating wastewaters.

Highly efficient copper(II) ion sorbents obtained by calcium carbonate mineralization on functionalized cross-linked copolymers.

A new type of Cu(II) ion sorbents is presented. These are obtained by CaCO3 mineralization from supersaturated solutions on gel-like cross-linked polymeric beads as insoluble templates. A divinylbenzene-ethylacrylate-acrylonitrile cross-linked copolymer functionalized with weakly acidic, basic, or amphoteric functional groups has been used, as well as different initial inorganic concentrations and addition procedures for CaCO3 crystal growth. The morphology of the new composites was investigated by SEM and compared to that of the unmodified beads, and the polymorph content was established by X-ray diffraction. The beads, before and after CaCO3 mineralization, were tested as sorbents for Cu(II) ions. The newly formed patterns on the bead surface after Cu(II) sorption were observed by SEM, and the elemental distribution on the composites and the chemical structure of crystals after interaction with Cu(II) were investigated by EDAX elemental mapping and by FTIR-ATR spectroscopy, respectively. The sorption capacity increased significantly after CaCO3 crystals growth on the weak anionic bead surface (up to 1041.5 mg Cu(II) /g sample) compared to that of unmodified beads (491.5 mg Cu(II) /g sample).

Decolorization of ammonium lignosulfonate with H(2)O(2)/Cu(II) heterogeneous catalyst.

The potential of ammonium lignosulfonate (ALS) decolorization and degradation in aqueous solution was studied in a heterogeneous system using hydrogen peroxide and a Cu (II)-chelating ion exchanger. This was based on acrylic copolymers functionalized with N,N dimethylamino propylamine (DMAPA) as a catalyst. In order to optimize the efficiency of the system, the influence of such process parameters like H(2)O(2) concentration, pH, contact time, temperature, ALS concentration and catalyst amount were evaluated. The apparent rate constant of decolorization calculated from the absorbance data indicates that the process profiles follow pseudo-first order kinetics. Lignosulfonate degradation was furthermore studied by FTIR spectroscopy, thermogravimetric analysis and determination in phenolic compounds. The catalyst stability and reusability have also been investigated. Our experimental results clearly indicate that, under optimum conditions, the ammonium lignosulfonate solutions exhibit a total bleaching associated with degradation and significant mineralization to CO(2).

Platinum (IV) recovery from chloride solution by functionalized acrylic copolymers.

Two acrylic adsorbents with different morphological structures and bearing amidoethylenamine and thiol groups were obtained and used for platinum sorption from chloride solution by the batch method. Physico-chemical parameters that influence adsorption such as initial Pt(IV) concentration, stirring time, pH, and adsorbent amount were investigated. The thermodynamic parameters of Pt(IV) sorption on the synthesized adsorbent were also evaluated based on Langmuir and Freundlich isotherms. Thermodynamic parameters estimated from Langmuir constants indicated that the adsorption is spontaneous, exothermic and there is a disordered state at the molecular level. The models used to analyze the sorption rate led to the conclusion that the most important step in the sorption of Pt(IV) could be both particle diffusion and chemical reaction of [PtCl(6)](-) with amine functional groups. Thus, both the ion exchange and complex formation mechanisms can occur via nitrogen atoms in the recovery of Pt(IV) on the studied adsorbent.

Sorption studies of chromium(VI) onto new ion exchanger with tertiary amine, quaternary ammonium and ketone groups.

A new acrylic anion exchanger with both tertiary and quaternary ammonium as well as ketone groups in the structural unit has been prepared by the nucleophilic substitution reaction of aminolyzed vinylacetate:acrylonitrile:divinylbenzene copolymer of porosity structure in the swelling state with 2-chloroacetone as a halogenated compound. The new compound exhibits better qualities of strong base exchange capacity than the weak base anion exchangers. The obtained acrylic anion exchanger was used to remove Cr(VI) from the aqueous solution. Batch adsorption studies have been carried out to determine the effect of contact time, concentration of hexavalent chromium in the solution and pH on the sorption capacity. The kinetic parameters were determined on the basis of the static results. The thermodynamic parameters of Cr(VI) sorption process on the anion exchanger were calculated based on the Langmuir and Freundlich isotherms. Sorption was studied in the pH range of 1.5-7 and it was found that it depends on the solution acidity. At the pH values of 3.5 and 7 the anion exchanger exhibited large values of chromium sorption capacity. The speciation of chromium was investigated in the studied pH range by the Diffuse Reflectance Spectroscopy (DRS) method. Reduction of chromium(VI) to chromium(III) under acidic conditions was observed. The performed acrylic strong base anion exchanger is superior compared to the conventional one based on the styrene:divinylbenzene matrix due to its ability for reposition of the long spacer arm for providing exchange sites, hydrophilic character of matrix, and possible hydrogen bonds provided by carbonyl functional groups.