Bioaccumulation and ecotoxicity of carbon nanotubes

Carbon nanotubes (CNT) have numerous industrial applications and may be released to the environment. In the aquatic environment, pristine or functionalized CNT have different dispersion behavior, potentially leading to different risks of exposure along the water column. Data included in this review indicate that CNT do not cross biological barriers readily. When internalized, only a minimal fraction of CNT translocate into organism body compartments. The reported CNT toxicity depends on exposure conditions, model organism, CNT-type, dispersion state and concentration. In the ecotoxicological tests, the aquatic organisms were generally found to be more sensitive than terrestrial organisms. Invertebrates were more sensitive than vertebrates. Single-walled CNT were found to be more toxic than double-/multi-walled CNT. Generally, the effect concentrations documented in literature were above current modeled average environmental concentrations. Measurement data are needed for estimation of environmental no-effect concentrations. Future studies with benchmark materials are needed to generate comparable results. Studies have to include better characterization of the starting materials, of the dispersions and of the biological fate, to obtain better knowledge of the exposure/effect relationships

Solar-powered production of molecular hydrogen from water

Electrochemical water splitting powered by conventional electricity or photovoltaic arrays produces molecular hydrogen at the cathode, while organic compound oxidation under mild conditions takes place at the anode in competition with the production of oxygen. An electrolytic cell, which is based on the coupling of bismuth-doped titanium dioxide anodes (BiOx-TiO2) With stainless steel (SS) cathodes, is characterized in terms of hydrogen production efficiency and organic compound degradation. In the solar-powered photovoltaic (PV)-electrochemical system, the production of molecular oxygen at the anode is suppressed by the simultaneous oxidation and mineralization of organic compounds dissolved in water. In addition, the anodic oxidation of organic substrates has a synergistic effect on hydrogen production at the cathode that results in a 53% increase in the energy efficiency for H-2 generation at circum-neutral PH in the presence of dilute electrolyte solutions.X114732sciescopu

Reductive Defluorination of Aqueous Perfluorinated Alkyl Surfactants: Effects of Ionic Headgroup and Chain Length

Perfluorinated chemicals (PFCs) are distributed throughout the environment. In the case of perfluorinated alkyl carboxylates and sulfonates, they can be classified as persistent organic pollutants since they are resistant to environmentally relevant reduction, oxidation, and hydrolytic processes. With this in mind, we report on the reductive defluorination of perfluorobutanoate, PFBA (C3F7CO2-), perfluorohexanoate, PFHA (C5F11CO2-), perfluorooctanoate, PFOA (C7F15CO2-), perfluorobutane sulfonate, PFBS (C4F9SO3-), perfluorohexane sulfonate, PFHS (C6F13SO3-), and perfluorooctane sulfonate, PFOS (C8F17SO3-) by aquated electrons, e(aq)(-), that are generated from the UV photolysis (lambda = 254 nm) of iodide. The ionic headgroup (-SO3- vs -CO2-) has a significant effect on the reduction kinetics and extent of defluorination (F index = -[F-](produced)/ [PFC](degraded)). Perfluoroalkylsulfonate reduction kinetics and the F index increase linearly with increasing chain length. In contrast, perfluoroalkylcarboxylate chain length appears to have a negligible effect on the observed kinetics and the F index. H/F ratios in the gaseous fluoro-organic products are consistent with measured F indexes. Incomplete defluorination of the gaseous products suggests a reductive cleavage of the ionic headgroup occurs before complete defluorination. Detailed mechanisms involving initiation by aquated electrons are proposed.X119899sciescopu

Simultaneous multifunctional sorption of PFOS and Cr(VI) on activated carbon prepared by one-step microwave activation

Multifunctional sorbents, activated carbons (AC), were prepared by one-step microwave activation utilizing peanut shells and sunflower seed husks. The influence of the original particle size of raw materials on the yield and specific surface area of AC was studied, which reached 33.5 % and 1133.27 m(2)/g, respectively. The repetitive and competitive uptakes of perfluorooctane sulfonate (PFOS) and chromium were applied to investigate the sorption properties of AC. The sorption mechanisms were demonstrated using sulfur Kedge X-ray absorption near edge structure analysis (XANES). In the repetitive experiment, AC made from peanut shells (AC(P05)) still retained 70 % removal efficiency of PFOS after the fourth sorption because sorbed PFOS might form a new organic phase that supplied effective sites for the hydrophobic partition of PFOS. However, the removal efficiency of Cr(VI) decreased dramatically from 60 to 11 % after the fourth uptake because electrostatic attraction was its only removal pathway. In the binary solutes system, AC(P05) possessed perfect sorption performance for both PFOS and Cr(VI), which were 885 and 192 mg/g, respectively. In the multivariate solutes system, the XANES spectra indicated that the thiol functional group existed in the resulting AC and a metal chelate was formed between thiol and Zn2+/Cu2+. Hence, the presence of Zn2+/Cu2+ further promoted the removal of PFOS and Cr(VI) through the electrostatic attraction between the anions and positive metal chelate