This study aims to investigate factors leading to agglomeration of citrate coated silver (AgNP-Cit), polyvinylpyrrolidone coated AgNPPVP and titanium dioxide (TiO2) nanoparticles in surface waters and wastewater. ENPs (1 mg/L) were spiked to unfiltered, filtered, ultrafiltered (<10 kDa and <1 kDa) samples. Z-average particle sizes were measured after 1 h, 1 day and 1 week. AgNP-PVP was stable in all fractions of the samples and kept their original size around 60 nm over 1 week. Agglomeration of AgNP-Cit and TiO2 was positively correlated with Ca2+ concentration, but dissolved organic carbon concentrations > 2 mg/L contributed to stabilizing these NP. Moreover, agglomeration of AgNP-Cit in the various organic matter fractions showed that high molecular weight organic compounds such as biopolymers provide stabilization in natural water. A generalized scheme for the agglomeration behavior of AgNP-Cit, AgNP-PVP and TiO2 in natural waters was proposed based on their relation with Ca2+, Mg2+ and DOC concentration.

For twenty-five world lakes and three engineered nanoparticles (ENP), lake retention was calculated using a uniformly mixed lake mass balance model. This follows similar approaches traditionally used in water quality management. Lakes were selected such that lake residence times, depths and areal hydraulic loadings covered the widest possible range among existing lakes. Sedimentation accounted for natural colloid as well as suspended solid settling regimes. An ENP-specific mixed sedimentation regime is proposed. This regime combines ENP sedimentation through slow settling with natural colloids from the water column, with faster settling with suspended solids from a selected part of the water column. Although sedimentation data and hydrodynamic concepts as such were not new, their first time combination for application to ENPs shows in which cases lake retention is important for these particles. In combination with ENP emission data, lake retention translates directly into potential risks of ENPs for lake benthic communities.

We investigated effects of Ag2S engineered nanomaterials (ENMs), polyvinylpyrrolidone (PVP) coated Ag ENMs (PVP-Ag), and Ag+ on arbuscular mycorrhizal fungi (AMF), their colonization of tomato (Solanum lycopersicum), and overall microbial community structure in biosolids-amended soil. Concentration-dependent uptake was measured in all treatments. Plants exposed to 100 mg kg−1 PVP-Ag ENMs and 100 mg kg−1 Ag+ exhibited reduced biomass and greatly reduced mycorrhizal colonization. Bacteria, actinomycetes and fungi were inhibited by all treatment classes, with the largest reductions measured in 100 mg kg−1 PVP-Ag ENMs and 100 mg kg−1 Ag+. Overall, Ag2S ENMs were less toxic to plants, less disruptive to plant-mycorrhizal symbiosis, and less inhibitory to the soil microbial community than PVP-Ag ENMs or Ag+. However, significant effects were observed at 1 mg kg−1 Ag2S ENMs, suggesting that the potential exists for microbial communities and the ecosystem services they provide to be disrupted by environmentally relevant concentrations of Ag2S ENMs.

Silver nanoparticles (Ag-NPs) are among the most produced NPs worldwide having several applications in consumer products. Ag-NPs are known to cause oxidative stress in several organisms and cell lines, however comparatively less information is available regarding their effects on soil living invertebrates. The purpose of this study was to investigate if Ag-NPs cause oxidative stress on soil invertebrates. The model soil species Eisenia fetida was used. Our results showed that total glutathione (TG) is the first mechanism triggered by Ag-NPs, followed by glutathione peroxidase (GPx) and glutathione reductase (GR), however oxidative damage was observed for higher doses and exposure time (increased lipid peroxidation, LPO). AgNO3 exposure caused impairment in GPx and glutathione-S-transferase (GST), probably as result of the higher bioavailability of Ag in the salt-form. The current results indicate that effects are partly caused by Ag ions released from Ag-NPs, but specific particle effects cannot be excluded.

Inspired by the adhesion of marine mussels, a kind of superhydrophobic oil sorbent was successfully fabricated by robustly immobilizing the micro/nanostructure layer onto the sponge skeleton. The as-prepared sponges possess excellent hydrophobicity with the water contact angle of 154°, which enables the sponge to selectively absorb various oils floating on water surface. The oil sorption capacities of as-prepared sponge for a series of oils can reach 18.3–46.8g/g. The absorbed oil can be recovered by mechanical squeezing and the resulting sponge can be recycled more than 70 cycles while still keeping high oil sorption capability. More importantly, the obtained sponge has excellent affinity to the high viscosity oils. Therefore, the as-prepared sponge might find practical applications in the large-scale removal of oils especially high viscosity oils from water surface.

In this study, natural calcium-rich attapulgite (NCAP) was used to develop a low-cost adsorbent for removing fluoride (F⁻) from contaminated water. The results showed that calcination can dramatically increase the F⁻ sorption capacity of NCAP and that the maximum F⁻ sorption capacity occurred at 700 °C. The sorption of F⁻ on NCAP heated at 700 °C (NCAP700) followed pseudo-second-order kinetics and was described by the Langmuir equilibrium model. The estimated F⁻ sorption capacity was approximately 140.0 mg/g at pH 8.0, which was comparable with the sorption capacities of some nanomaterials. The sorption of F⁻ on NCAP700 performed well at pH values of 7 to 10. In addition, anions such as NO₃ ⁻ and SO₄ ²⁻ did not affect fluoride removal, but PO₄ ³⁻ and HCO₃ ⁻ moderately influenced fluoride removal. A column study conducted using NCAP700 with a particle size of 0.2–0.5 mm indicated that the adsorbent could effectively purify nearly 200 bed volumes (BV) of water containing 3.0 mg F/l at pH 8.5. The removal of F⁻ from water mainly resulted from the formation of calcium fluoride precipitates and the complexation of fluoride with the –OH group of NCAP700, which was further confirmed by scanning electron microscopy–energy dispersive spectrometry (SEM-EDS) and X-ray photoelectron spectroscopy (XPS).

For the last 10 years, engineered nanomaterials (ENMs) have raised interest to industrials due to their properties. They are present in a large variety of products from cosmetics to building materials through food additives, and their value on the market was estimated to reach $3 trillion in 2014 (Technology Strategy Board 2009). TiO₂ NMs represent the second most important part of ENMs production worldwide (550–5500 t/year). However, a gap of knowledge remains regarding the fate and the effects of these, and consequently, impact and risk assessments are challenging. This is due to difficulties in not only characterizing NMs but also in selecting the NM properties which could contribute most to ecotoxicity and human toxicity. Characterizing NMs should thus rely on various analytical techniques in order to evaluate several properties and to crosscheck the results. The aims of this review are to understand the fate and effects of TiO₂ NMs in water, sediment, and soil and to determine which of their properties need to be characterized, to assess the analytical techniques available for their characterization, and to discuss the integration of specific properties in the Life Cycle Assessment and Risk Assessment calculations. This study underlines the need to take into account nano-specific properties in the modeling of their fate and effects. Among them, crystallinity, size, aggregation state, surface area, and particle number are most significant. This highlights the need for adapting ecotoxicological studies to NP-specific properties via new methods of measurement and new metrics for ecotoxicity thresholds.