Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Niksa Odzak is active.

Publication


Featured researches published by Niksa Odzak.


Environmental Pollution | 2014

Dissolution of metal and metal oxide nanoparticles in aqueous media

Niksa Odzak; David Kistler; Renata Behra; Laura Sigg

The dissolution of Ag (citrate, gelatin, polyvinylpyrrolidone and chitosan coated), ZnO, CuO and carbon coated Cu nanoparticles (with two nominal sizes each) has been studied in artificial aqueous media, similar in chemistry to environmental waters, for up to 19 days. The dissolved fraction was determined using DGT (Diffusion Gradients in Thin films), dialysis membrane (DM) and ultrafiltration (UF). Relatively small fractions of Ag nanoparticles dissolved, whereas ZnO dissolved nearly completely within few hours. Cu and CuO dissolved as a function of pH. Using DGT, less dissolved Ag was measured compared to UF and DM, likely due to differences in diffusion of organic complexes. Similar dissolved metal concentrations of ZnO, Cu and CuO nanoparticles were determined using DGT and UF, but lower using DM. The results indicate that there is a need to apply complementary techniques to precisely determine dissolution of nanoparticles in aqueous media.


Aquatic Sciences | 2002

In situ trace metal speciation in a eutrophic lake using the technique of diffusion gradients in thin films (DGT)

Niksa Odzak; David Kistler; Hanbin Xue; Laura Sigg

Abstract. We evaluated the application of DGT (diffusion gradients in thin films) as a tool to determine Cu, Zn, Ni, Cd, Pb and Mn concentrations and speciation in a hardwater eutrophic lake. This technique was used in situ during six sampling periods over one year in Lake Greifen. The DGT-labile species of Cu and Ni amounted to 15–25% of the total dissolved concentrations. Speciation by ligand-exchange/DPCSV indicated that Cu and Ni were predominantly organically complexed (>99%). Thus, the DGT-labile species for Cu and Ni were much more abundant than the free ionic and inorganic species determined by ligand-exchange/DPCSV. The results can be explained by incomplete metal exchange of very strong complexes with the chelating resin in the DGT devices, metal exchange of less abundant weaker complexes, and by slow diffusion of exchangeable organic complexes. For Zn (36 to >90% DGT-labile) and Mn (50 to 100% DGT-labile), the results indicated that these metals are less strongly organically complexed. A larger fraction of Zn occurred in DGT-labile species in the hypolimnion than it did in the surface water, probably due to a larger concentration of strong ligands in the productive surface water. DGT-labile Cd- (0.01–0.02 nM) and Pb-species (0.03–0.06 nM) were detected at very low levels. The combination of measurements of dissolved and DGT-labile species showed a decrease of Cu, Zn, Cd and Mn concentration at 2.5 m from June to August, which was probably linked to intensive sedimentation of organic matter during summer stagnation. Mixing and oxygenation of the lake in winter-spring led to an increase in dissolved and DGT-labile Ni, Zn and Cd, whereas Mn decreased in the hypolimnion.


Environmental Science & Technology | 2015

Effects of Differently Coated Silver Nanoparticles on the Photosynthesis of Chlamydomonas reinhardtii

Enrique Navarro; Bettina Wagner; Niksa Odzak; Laura Sigg; Renata Behra

Various factors have been invoked to explain the toxicity of silver nanoparticles (AgNP) to microorganisms including particle size and the nature of stabilizing coatings as well as the amount of dissolved silver occurring in AgNP suspensions. In this study we have assessed the effects of nine differently coated AgNP (chitosan, lactate, polyvinylpyrrolidone, polyethelene glycol, gelatin, sodium dodecylbenzenesulfonate, citrate, dexpanthenol, and carbonate) and AgNO3 on the photosynthesis of the freshwater algae Chlamydomonas reinhardtii. We have thus examined how AgNP effects on algae relate to particle size, measured dissolved silver (Agd), and bioavailable silver (Agbioav). Agbioav was indirectly estimated in toxicity experiments by cysteine-silver complexation at the EC50. The EC50 calculated as a function of measured Agd concentrations showed for some coatings values similar to that of dissolved Ag, whereas other coated AgNP displayed lower EC50 values. In all cases, excess cysteine completely prevented effects on photosynthetic yield, confirming the role of Agd as a cause of the observed effect on the photosynthesis. Toxicity was related neither to particle size nor to the coatings. For all differently coated AgNP suspensions, the EC50 values calculated as a function of Agbioav were comparable to the value of AgNO3. Depending on the coatings Agbioav was comparable to or higher than measured Agd.


Environmental Toxicology and Chemistry | 2009

Kinetics of cadmium accumulation in periphyton under freshwater conditions

Philippe Bradac; Enrique Navarro; Niksa Odzak; Renata Behra; Laura Sigg

The aim of the present study was to investigate the kinetics of cadmium (Cd) accumulation (total and intracellular) in periphyton under freshwater conditions in a short-term microcosm experiment. Periphyton was precolonized in artificial flow-through channels supplied with natural freshwater and then exposed for 26.4 h to nominal Cd concentrations of 5 and 20 nM added to natural freshwater. Labile Cd in water determined with diffusion gradient in thin films was 60 to 69% of total dissolved Cd in the exposure channels and 11% in the control channel. Intracellular Cd concentrations in periphyton increased rapidly and linearly during the first 71 min. Initial intracellular uptake rates were 0.05 and 0.18 nmol of Cd/g of dry weight × min in the 5 nM and 20 nM exposures, respectively. The subsequent intracellular uptake was slower, approaching steady state at the end of Cd exposure. Uptake kinetics of Cd was slower when compared to experiments with planktonic algal cultures, probably due to diffusion limitations. Intracellular Cd uptake during the entire exposure was modeled with a nonlinear, one-compartment model from which uptake and clearance rate constants, as well as bioconcentration factors, were obtained. The release of Cd from periphyton after the end of Cd exposure was slow when compared to the initial uptake rates.


Environmental Chemistry | 2015

Dissolution of metal and metal oxide nanoparticles under natural freshwater conditions

Niksa Odzak; David Kistler; Renata Behra; Laura Sigg

Environmental context Engineered nanomaterials (e.g. silver, zinc oxide and copper oxide) are being widely used in many consumer products such as cosmetics, food packaging and textiles. During their usage and treatment, they will be released to natural waters and partly dissolve, depending on the water type and nanomaterial characteristics. These nanomaterials may thus have some toxic effects to aquatic organisms and indirectly to humans because of higher concentrations of dissolved silver, zinc and copper in natural waters. Abstract The dissolution of some widely used nanoparticles (NPs), Ag (citrate coated), ZnO, CuO and Cu-carbon coated (Cu/C), has been studied over a period of 9 days in five different natural waters: wastewater treatment plant effluent (WWTP Dubendorf) and lakes Greifen, Lucerne, Gruere and Cristallina. These waters differ in ionic strength, pH and dissolved organic carbon (DOC). The dissolved fraction of metals from NPs was determined using DGT (diffusion gradients in thin films) and ultrafiltration (UF). ZnO-NPs and CuO-NPs dissolved to a large extent in all waters, whereas the dissolved fraction was much smaller in the case of Cu/C and Ag-NPs. All NPs dissolved to a larger extent in water from Lake Cristallina with low pH, low ionic strength and low DOC. Ag-NP dissolution was favoured at low ionic strength and low pH, whereas dissolution of CuO-NPs was mostly dependent on pH. Cu/C-NPs strongly agglomerated and sedimented and yielded low dissolved Cu concentrations. DGT and UF produced similar results, although these two methods differ in the measurement time scale. The results of this study indicate that dissolution is an important process for these NPs under conditions of natural waters or wastewaters.


Chimia | 2014

Chemical Aspects of Nanoparticle Ecotoxicology.

Laura Sigg; Renata Behra; Ksenia J. Groh; Carl Isaacson; Niksa Odzak; Flavio Piccapietra; Lena Röhder; Hannah Schug; Yang Yue; Kristin Schirmer

Nanoecotoxicology strives to understand the processes and mechanisms by which engineered nanoparticles (ENP) may exert toxic effects on aquatic organisms. Detailed knowledge of the chemical reactions of nanoparticles in the media and of their interactions with organisms is required to understand these effects. The processes of agglomeration of nanoparticles, of dissolution and release of toxic metal ions, and of production of reactive oxygen species (ROS) are considered in this article. Important questions concern the role of uptake of nanoparticles in various organisms, in contrast to uptake of ions released from nanoparticles and to nanoparticle attachment to organism surfaces. These interactions are illustrated for effects of silver nanoparticles (AgNP), cerium oxide (CeO2 NP) and titanium dioxide (TiO2 NP), on aquatic organisms, including algae, biofilms, fish cells and fish embryos.


Environmental Science & Technology | 2008

Toxicity of silver nanoparticles to Chlamydomonas reinhardtii.

Enrique Navarro; Flavio Piccapietra; Bettina Wagner; Fabio Marconi; Ralf Kaegi; Niksa Odzak; Laura Sigg; Renata Behra


Environmental Science & Technology | 2006

Model predictions of metal speciation in freshwaters compared to measurements by in situ techniques.

Emily R. Unsworth; Kent W. Warnken; Hao Zhang; William Davison; Frank Black; Jacques Buffle; Jun Cao; R.F.M.J. Cleven; Josep Galceran; Peggy Gunkel; E.J.J. Kalis; David Kistler; Herman P. van Leeuwen; Michel Martin; Stéphane Noël; Yusuf Nur; Niksa Odzak; Jaume Puy; Willem H. van Riemsdijk; Laura Sigg; E.J.M. Temminghoff; Mary-Lou Tercier-Waeber; Stefanie Toepperwien; Raewyn M. Town; Liping Weng; Hanbin Xue


Environmental Science & Technology | 2006

Comparison of Analytical Techniques for Dynamic Trace Metal Speciation in Natural Freshwaters

Laura Sigg; Frank Black; Jacques Buffle; Jun Cao; R.F.M.J. Cleven; William Davison; Josep Galceran; Peggy Gunkel; E.J.J. Kalis; David Kistler; Michel Martin; Stéphane Noël; Yusuf Nur; Niksa Odzak; Jaume Puy; Willem H. van Riemsdijk; E.J.M. Temminghoff; Mary-Lou Tercier-Waeber; Stefanie Toepperwien; Raewyn M. Town; Emily R. Unsworth; Kent W. Warnken; Liping Weng; Hanbin Xue; Hao Zhang


Analytica Chimica Acta | 2004

Speciation of copper and zinc in natural freshwater: comparison of voltammetric measurements, diffusive gradients in thin films (DGT) and chemical equilibrium models

Sébastien Meylan; Niksa Odzak; Renata Behra; Laura Sigg

Collaboration


Dive into the Niksa Odzak's collaboration.

Top Co-Authors

Avatar

Laura Sigg

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar

David Kistler

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar

Renata Behra

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar

Enrique Navarro

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar

Hanbin Xue

École Polytechnique Fédérale de Lausanne

View shared research outputs
Top Co-Authors

Avatar

Bettina Wagner

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar

Flavio Piccapietra

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Jun Cao

Swiss Federal Institute of Aquatic Science and Technology

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge