Environmental and technical impacts of floating photovoltaic plants as an emerging clean energy technology.

Floating photovoltaic (FPV) plants present several benefits in comparison with ground-mounted photovoltaics (PVs) and could have major positive environmental and technical impacts globally. FPVs do not occupy habitable and productive areas and can be deployed in degraded environments and reduce land-use conflicts. Saving water through mitigating evaporation and improving water security in arid regions combined with the flexibility for deployment on different water bodies including drinking water reservoirs are other advantages of FPVs. They also have higher efficiency than ground-mounted PV solar and are compatible with the existing hydropower infrastructures, which supports diversifying the energy supply and its resilience. Despite the notable growth of FPVs on an international scale, lack of supporting policies and development roadmaps by the governments could hinder FPVs' sustainable growth. Long-term reliability of the floating structures is also one of the existing concerns that if not answered could limit the expansion of this emerging technology.

Effects of synthetic iron and aluminium oxide surface charge and hydrophobicity on the formation of bacterial biofilm.

In this research, bacterial cell attachments to hematite, goethite and aluminium hydroxide were investigated. The aim was to study the effects of these minerals' hydrophobicity and pH-dependent surface charge on the extent of biofilm formation using six genetically diverse bacterial strains: Rhodococcus spp. (RC92 & RC291), Pseudomonas spp. (Pse1 & Pse2) and Sphingomonas spp. (Sph1 & Sph2), which had been previously isolated from contaminated environments. The surfaces were prepared in a way that was compatible with the naturally occurring coating process in aquifers: deposition of colloidal particles from the aqueous phase. The biofilms were evaluated using a novel, in situ and non-invasive technique developed for this purpose. A manufactured polystyrene 12-well plate was used as the reference surface to be coated with synthesized minerals by deposition of their suspended particles through evaporation. Planktonic phase growth indicates that it is independent of the surface charge and hydrophobicity of the studied surfaces. The hydrophobic similarities failed to predict biofilm proliferation. Two of the three hydrophilic strains formed extensive biofilms on the minerals. The third one, Sph2, showed anomalies in contrast to the expected electrostatic attraction between the minerals and the cell surface. Further research showed how the solution's ionic strength affects Sph2 surface potential and shapes the extent of its biofilm formation; reducing the ionic strength from ≈200 mM to ≈20 mM led to a tenfold increase in the number of cells attached to hematite. This study provides a technique to evaluate biofilm formation on metal-oxide surfaces, under well-controlled conditions, using a simple yet reliable method. The findings also highlight that cell numbers in the planktonic phase do not necessarily show the extent of cell attachment, and thorough physicochemical characterization of bacterial strains, substrata and the aquifer medium is fundamental to successfully implementing any bioremediation projects.

Bimodal responses of cells to trace elements: insights into their mechanism of action using a biospectroscopy approach.

Understanding how organisms respond to trace elements is important because some are essential for normal bodily homeostasis, but can additionally be toxic at high concentrations. The inflection point for many of these elements is unknown and requires sensitive techniques capable of detecting subtle cellular changes as well as cytotoxic alterations. In this study, we treated human cells with arsenic (As), copper or selenium (Se) in a dose-response manner and used attenuated total reflection Fourier-transform infrared (ATR-FTIR) microspectroscopy combined with computational analysis to examine cellular alterations. Cell cultures were treated with As(V), Cu(2+) or Se(IV) at concentrations ranging from 0.001 mg L(-1) to 1000 mg L(-1) and their effects were spectrochemically determined. Results show that As(V) and Cu(2+) induce bimodal dose-response effects on cells; this is in line with hormesis-driven responses. Lipids and proteins seem to be the main cell targets for all the elements tested; however, each compound produced a unique fingerprint of effect. Spectral biomarkers indicate that all test agents generate reactive oxygen species (ROS), which could either stimulate repair mechanisms or induce damage in cells.

Measurement of ZnO nanoparticles using diffusive gradients in thin films: binding and diffusional characteristics.

Rapid growth in finding new applications for manufactured nanomaterials (MNM) has recently been accompanied by awareness about their related adverse toxicological and environmental impacts. Due to their intrinsic nature, measuring available concentrations of MNMs in the environment is a major challenge. This research is a launching point toward filling this gap, as it presents the potential of the well-established diffusive gradients in thin films (DGT) technique to determine MNMs concentrations in situ. Two binding layers commonly used in DGT devices were shown to be able to bind ZnO nanoparticles (ZnO NPs). The use of different types of diffusive layers demonstrated the critical role of their pore size for selective function of the DGT devices. The ZnO NPs can pass through the open pore diffusive layer used in standard DGT devices and be retained by the binding resin layer. However, the diffusion of ZnO NPs can be prevented when a 1000 MWCO (molecular weight cut off) dialysis membrane is placed in the front of the diffusive gel layer. A combination of two or more DGT devices with known diffusive layer properties should enable deduction of concentrations of available ZnO NPs in the environment. Unlike metal ions, determining diffusion coefficient values for ZnO NPs is challenging and greatly affected by shape, morphology, and solution-induced changes of the particles. Attenuated total reflection Fourier-transform infrared spectroscopy (ATR-FTIR) demonstrated that retention of ZnO NPs by Chelex and Metsorb binding layers occurs through chemisorption. The superior uptake kinetic for Chelex indicates that it is a better candidate for further development of DGT devices to measure ZnO NPs. These initial results are promising and important for further developing the DGT technique to measure available concentrations of manufactured nanomaterials in the different environmental media (waters, soils, and sediments). Further experiments investigating the effects of pH, ionic strength, and solution chemistry on the performance of DGT for measuring MNM concentrations are needed.

Evaluation of ATR-FTIR spectroscopy with multivariate analysis to study the binding mechanisms of ZnO nanoparticles or Zn2+ to Chelex-100 or metsorb.

Advancements in nanotechnology and the expected increases in production of commercial products with incorporated manufactured nanomaterials will very likely lead to increasing contamination of nanoparticles (NPs) in the environment. Though studying adverse impacts of NPs in the environment and their ecotoxicological fate and behavior is not new, limited information is available. A major challenge in this respect is the lack of a proper sampling technique that could provide data on concentrations of these materials in the environment. Diffusive gradient in thin-films (DGT) is a well-established method that can measure available concentrations of trace metals in soils and waters. Using this approach, different binding resins are employed as a sink to collect targeted chemicals during fixed times. Here, we examine the suitability of two common types of the DGT binding agents, commercially available Chelex-100 and Metsorb, to investigate whether these materials could irreversibly retain a model nanoparticle, ZnO, and if so, what would be the difference between bound ZnO NP and Zn(2+) ion. Attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy was used to study the binding materials before and after exposure to ZnO NP and Zn(2+). Based on computational analysis using principal component analysis and linear discriminant analysis (PCA-LDA), it was demonstrated that both Chelex-100 and Metsorb form chemical bonds with ZnO NP and Zn(2+), however the binding mechanisms of these zinc species as inferred from their infrared (IR) spectra are statistically different (95% confidence level). The experimental results suggest that the binding resins hold ZnO NP with fewer and weaker chemical bonds compared to Zn(2+). This research shows the potential of the DGT method to measure available concentrations of nanoparticles in the environment and demonstrate how ATR-FTIR spectroscopy, when used with computational analysis, can differentiate between diverse chemical species that are simultaneously retained by the binding layer in a DGT device.