Silica based inorganic-organic hybrid materials for the adsorptive removal of chromium.

We employed polymer functionalized silica gel as an adsorbent for the removal of Cr(vi) from water. The chains of 2-aminoethyl methacrylate hydrochloride (AEMA·HCl) polymer were grown from the surface of silica gel via surface-initiated conventional radical polymerization and the resulting hybrid material exhibited high affinity for chromium(vi). To investigate the adsorption behavior of Cr(vi) on diverse polymer based hybrid materials, the removal capacity of (SG-AEMH) was compared with our previously reported branched polyamine functionalized mesoporous silica (MS-PEI). The adsorption capacities of polymer based materials were also compared with their respective monolayer based platforms comprising a 3-aminopropyltriethoxysilane (APTES) functionalized silica gel (SG-APTES) and mesoporous silica (MS-APTES). The polymer based systems showed excellent Cr(vi) adsorption efficiencies compared to monolayer counterparts. The structural characteristics and surface modification of these adsorbents were examined by Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The experimental data were analyzed using the Langmuir and Freundlich models. Correlation coefficients were determined by analyzing each isotherm. The kinetic data of adsorption reactions were described by pseudo-first-order and pseudo-second-order equations. Thermodynamic parameters, i.e., change in the free energy (ΔG°), the enthalpy (ΔH°), and the entropy (ΔS°), were also evaluated. The synthesized hybrid materials exhibited a high adsorption capacity for chromium ions. Furthermore, they could be regenerated and recycled effectively.

Food web effects of titanium dioxide nanoparticles in an outdoor freshwater mesocosm experiment.

Over the course of 78 days, nine outdoor mesocosms, each with 1350 L capacity, were situated on a pontoon platform in the middle of a lake and exposed to 0 µg L(-1) TiO2, 25 µg L(-1) TiO2 or 250 µg L(-1) TiO2 nanoparticles in the form of E171 TiO2 human food additive five times a week. Mesocosms were inoculated with sediment, phytoplankton, zooplankton, macroinvertebrates, macrophytes and fish before exposure, ensuring a complete food web. Physicochemical parameters of the water, nutrient concentrations, and biomass of the taxa were monitored. Concentrations of 25 µg L(-1) TiO2 and 250 µg L(-1) TiO2 caused a reduction in available soluble reactive phosphorus in the mesocosms by 15 and 23%, respectively, but not in the amount of total phosphorus. The biomass of Rotifera was significantly reduced by 32 and 57% in the TiO2 25 µg L(-1) and TiO2 250 µg L(-1) treatments, respectively, when compared to the control; however, the biomass of the other monitored groups-Cladocera, Copepoda, phytoplankton, macrophytes, chironomids and fish-remained unaffected. In conclusion, environmentally relevant concentrations of TiO2 nanoparticles may negatively affect certain parameters and taxa of the freshwater lentic aquatic ecosystem. However, these negative effects are not significant enough to affect the overall function of the ecosystem, as there were no cascade effects leading to a major change in its trophic state or primary production.

Design and fabrication of branched polyamine functionalized mesoporous silica: an efficient absorbent for water remediation.

A novel branched polyamine (polyethyleneimine, PEI) functionalized mesoporous silica (MS) adsorbent is developed via a facile "grafting-to" approach. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FT-IR) spectroscopy verified the effective surface functionalization of MS with monolayer and polymer. The transmission electron microscopy (TEM) was employed to reveal the morphology of the fabricated materials. The adsorption behavior of the polyamine functionalized mesoporous silica (MS-PEI) is assessed against anionic dyes. The adsorbent characteristics of MS-PEI are compared with a monolayer platform comprising of 3-aminopropyltriethoxy silane (APTES) functionalized mesoporous silica (MS-APTES). The adsorption behavior of the MS-PEI and MS-APTES toward anionic dyes is further evaluated by studying the effect of adsorbent dosage, pH, contact time, and temperature. Langmuir and Freundlich isotherm models are employed to understand the adsorption mechanism. The obtained kinetic data support a pseudo-second-order adsorption behavior for both monolayer and polymer functionalized MS. The associated thermodynamic parameters (ΔG°, ΔH°, and ΔS°) reveal that the process of adsorption with MS-PEI is more spontaneous and energetically favored as compared to the adsorption with MS-APTES. Taken together, the novel adsorbent system derived from a combination of MS and branched polymer (MS-PEI) shows the higher absorption efficiency and capacity toward the anionic dyes than the monolayer based adsorbent (MS-APTES).