Assessing bioavailability levels of metals in effluent-affected rivers: effect of Fe(III) and chelating agents on the distribution of metal speciation

2016 ◽  
Vol 74 (4) ◽  
pp. 896-903 ◽  
Author(s):  
Shuping Han ◽  
Wataru Naito ◽  
Shigeki Masunaga

To assess the effects of Fe(III) and anthropogenic ligands on the bioavailability of Ni, Cu, Zn, and Pb, concentrations of bioavailable metals were measured by the DGT (diffusive gradients in thin films) method in some urban rivers, and were compared with concentrations calculated by a chemical equilibrium model (WHAM 7.0). Assuming that dissolved Fe(III) (<0.45 μm membrane filtered) was in equilibrium with colloidal iron oxide, the WHAM 7.0 model estimated that bioavailable concentrations of Ni, Cu, and Zn were slightly higher than the corresponding values estimated assuming that dissolved Fe(III) was absent. In contrast, lower levels of free Pb were predicted by the WHAM 7.0 model when dissolved Fe(III) was included. Estimates showed that most of the dissolved Pb was present as colloidal iron–Pb complex. Ethylene-diamine-tetra-acetic acid (EDTA) concentrations at sampling sites were predicted from the relationship between EDTA and the calculated bioavailable concentration of Zn. When both colloidal iron and predicted EDTA concentrations were included in the WHAM 7.0 calculations, dissolved metals showed a strong tendency to form EDTA complexes, in the order Ni > Cu > Zn > Pb. With the inclusion of EDTA, bioavailable concentrations of Ni, Cu, and Zn predicted by WHAM 7.0 were different from those predicted considering only humic substances and colloidal iron.

2011 ◽  
Vol 8 (5) ◽  
pp. 517 ◽  
Author(s):  
Jacqueline Levy ◽  
Hao Zhang ◽  
William Davison ◽  
Rene Groben

Environmental context Interaction of metals with dissolved organic matter is one of the key processes defining metal bioavailability in water. The technique of diffusive gradients in thin films was used to investigate the kinetics of the interaction between metals and dissolved organic matter released by algae. For most metals the rate at which they were released from the organic matter was fast, but release of iron was kinetically limited. AbstractThe interaction of metals with organic matter is one of the key processes determining metal speciation and bioavailability in water. Fulvic acid tends to dominate dissolved organic carbon (DOC) in freshwaters, but organic carbon produced in situ, e.g. exudates released by algae and bacteria, is also significant. The technique of diffusive gradients in thin films (DGT) was used to investigate the lability of metal–exudate complexes using a kinetic signature approach. Exudates were harvested from three cultured freshwater alga (Chlorella vulgaris, Cryptomonas pyrenoidifera, Anabaena flos-aquae) and the filtered media supplemented with trace metals. DGT-labile metal concentrations and kinetic signatures were determined (24-h deployment). The relationship between Fe and DOC was a defining feature of the kinetic signatures. Iron was the most kinetically limited metal followed by Al and Cu, whereas Co, Ni and Pb were effectively completely labile. Exudates from Chlorella vulgaris produced the most DOC and the most marked kinetic limitation.


2012 ◽  
Vol 77 ◽  
pp. 343-347
Author(s):  
Daniela Lorenzo ◽  
Despina Fragouli ◽  
George C. Anyfantis ◽  
Roberto Cingolani ◽  
Athanassia Athanassiou

We present the fabrication of magnetic elastomeric membranes consisting of aligned superparamagnetic microwires embedded in a polymeric matrix. The wires are formed by the magnetic assembly of colloidal iron oxide nanoparticles (NPs) dispersed in the prepolymer matrix, during the curing of the polymer and the solvent evaporation. The appropriate combination of the NPs quantity and of the viscosity of the matrix results in the formation of thin membranes of about 10mm, containing few layers of aligned wires which after the polymer curing are blocked in fixed position into the matrix. The orientation and the dimensions of the magnetic wires depend on the direction and intensity of the external MF respectively.


2012 ◽  
Vol 12 (11) ◽  
pp. 5505-5512 ◽  
Author(s):  
Davide Altamura ◽  
Václav Holý ◽  
Dritan Siliqi ◽  
Indira Chaitanya Lekshmi ◽  
Concetta Nobile ◽  
...  

2009 ◽  
Vol 36 (4) ◽  
pp. 709-719 ◽  
Author(s):  
Siranee Sreesai ◽  
Suthipong Sthiannopkao

Utilization of zeolite industrial wastewater as a sorbent and (or) precipitant to remove Cu and Zn from copper-brass pipe industrial wastewater was conducted. These wastewaters were sampled and values for pH, temperature, biochemical oxygen demand (BOD5), chemical oxygen demand (COD), total solids (TS), total dissolved solids (TDS), total suspended solids (TSS), and heavy metals were determined. In addition, the sorption isotherms of Cu and Zn in copper-brass pipe industrial wastewater onto solids of zeolite industrial wastewater at various dilutions of copper-brass pipe industrial wastewater were explored. The relationship between Cu and Zn concentrations and their removal efficiencies under different conditions of wastewater pH, contact times, and ratios between copper-brass pipe industrial wastewater and zeolite industrial wastewater was examined. Zeolite industrial wastewater contained various carbonate compounds that contributed to high pH and TDS values, and low heavy metals contamination whereas copper-brass pipe industrial wastewater had a low pH value and was contaminated with heavy metals, especially Cu and Zn. Application of zeolite industrial wastewater significantly increased the pH of copper-brass pipe industrial wastewater and consequently removed Cu and Zn. The increase in pH of the wastewater mixture significantly enhanced the heavy metals removal. The Langmuir equation described sorption isotherms of Cu and Zn onto solids of zeolite industrial wastewater at neutral pH (6–7) while the Freundlich equation fitted well at pH > 12. The maximum Cu (97%–98%) and Zn (92%–96%) removal efficiencies occurred at the original pH 12.8 of zeolite industrial wastewater, at the ratio of copper-brass pipe industrial wastewater to zeolite industrial wastewater 3:1 (vol.:vol.) and at 30 min contact time.


2002 ◽  
Vol 09 (01) ◽  
pp. 437-440 ◽  
Author(s):  
F. NOLTING ◽  
J. LÜNING ◽  
J. ROCKENBERGER ◽  
J. HU ◽  
A. P. ALIVISATOS

A common limitation in nanostructure research is often the requirement to perform experiments on ensembles of nanoparticles, therefore averaging over inherent distributions with respect to particle size and shape, chemical composition, crystallinity and defect structure. This limitation can be overcome by studying the properties of a single nanostructure individually, which will allow one to truly correlate scaling laws of material properties with changes in size. Here we report the first experiments to explore the feasibility of spectromicroscopy using a photoemission electron microscope (PEEM) to record the X-ray absorption spectra of single nanocrystals. Colloidal iron oxide nanocrystals with an average diameter and standard deviation of 13 nm and 2 nm, respectively, were deposited on graphite (HOPG) forming small islands of agglomerated γ- Fe 2 O 3 nanocrystals (4–30 particles) as determined by scanning electron microscopy. Spatially resolved soft X-ray absorption spectra at the Fe L 3,2 edges of these individual islands were recorded with the PEEM2 instrument of the Advanced Light Source (ALS).


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