Synthetic Freshwater Research Articles

Diatom-derived extracellular polymeric substances form eco-corona and enhance stability of silver nanoparticles.

Silver nanoparticles (nAg) are extensively used across various fields and are frequently introduced into aquatic environments, where their behavior depends on environmental conditions. Extracellular polymeric substances (EPS) derived from aquatic organisms, such as diatoms, could play an important yet to be explored role in shaping the fate of nAg in aquatic environments. This study investigates the interactions between EPS, particularly those from the diatom Cyclotella meneghiniana, and citrate-coated nAg. The main objective is to understand how EPS influence the behaviours of nAg in freshwater settings, in terms of modulation of the nAg surface properties, colloidal stability and dissolution. To achieve these objectives a combination of the state-of-the-art spectroscopic and imaging techniques was employed. nAg was incubated with EPS isolated from an axenic C. meneghiniana culture, and their interactions were explored in a simulated freshwater environment over both short-term (0-2 h) and long-term (0-72 h) periods. The study focused on the changes in nAg, examining surface modulation, colloidal stability, dissolution, EPS adsorption on nAg, and the resulting eco-corona formation. The results indicate that EPS enhance the colloidal stability of nAg and decrease their dissolution in synthetic freshwater by adsorbing onto their surface and inducing steric repulsion between nAg particles. Visualization of the eco-corona formed by diatom EPS on nAg and its impact on aggregation processes is achieved through transmission electron microscopy. The formation of the EPS corona is attributed to the presence of diverse biopolymers within EPS, particularly proteins and polysaccharides. Fluorescence quenching studies on protein fluorophores demonstrate the formation, through hydrophobic interactions, of protein-nAg complex, further confirmed by AF4-DAD-FLD-ICP-MS. In a broader context, the results of this mechanistic study imply that diatoms, through the release of EPS, may significantly influence the destiny and possibly the bioavailability of nAg in EPS-abundant aquatic environments.

Eco-corona-mediated transformation of nano-sized Y2O3 in simulated freshwater: A short-term study

The use of metal and metal oxide nanomaterials (NMs) is experiencing a significant surge in popularity due to their distinctive structures and properties, making them highly attractive for a wide range of applications. This increases the risks of their potential negative impact on organisms if dispersed into the environment. Information about their behavior and transformation upon environmental interactions in aquatic settings is limited. In this study, the influence of naturally excreted biomolecules from the zooplankton Daphnia magna on nanosized Y2O3 of different concentrations was systematically examined in synthetic freshwater in terms of adsorption and eco-corona formation, colloidal stability, transformation, dissolution, and ecotoxicity towards D. magna. The formation of an eco-corona on the surface of the Y2O3 NMs leads to improved colloidal stability and a reduced extent of dissolution. Exposure to the Y2O3 NMs lowered the survival probability of D. magna considerably. The ecotoxic potency was slightly reduced by the formation of the eco-corona, though shown to be particle concentration-specific. Overall, the results highlight the importance of systematic mechanistic and fundamental studies of factors that can affect the environmental fate and ecotoxic potency of NMs.

Extraction and concentration of nanoplastic particles from aqueous suspensions using functionalized magnetic nanoparticles and a magnetic flow cell

Although a considerable knowledge base exists for environmental contamination from nanoscale and colloidal particles, significant knowledge gaps exist regarding the sources, transport, distribution, and effects of microplastic pollution (plastic particles < 5 mm) in the environment. Even less is known regarding nanoplastic pollution (generally considered to be plastic particles < 1 μm). Due to their small size, nanoplastics pose unique challenges and potential risks. We herein report a technique focused on the concentration and measurement of nanoplastics in aqueous systems. Hydrophobically functionalized magnetic nanoparticles (HDTMS-FeNPs) were used as part of a method to separate and concentrate nanoplastics from environmentally relevant matrices, here using metal-doped polystyrene nanoplastics (PAN-Pd@NPs) to enable low-level detection and validation of the separation technique. Using a magnetic separation flow cell, PAN-Pd@NPs were removed from suspensions and captured on regenerated cellulose membranes. Depending on the complexity of solution chemistry, variable extraction rates were possible. PAN-Pd@NPs were recovered from ultrapure water, synthetic freshwater, synthetic freshwater with a model natural organic matter isolate (NOM; Suwannee River Humic Acid), and from synthetic marine water, with recoveries for PAN-Pd@NPs of 84.9%, 78.9%, 70.4%, and 56.1%, respectively. During the initial method testing, it was found that the addition of NaCl was needed in the ultrapure water, synthetic freshwater and synthetic fresh water with NOM to induce particle aggregation and attachment. These results indicate that magnetic nanoparticles in combination with a flow-through system is a promising technique to extract nanoplastics from aqueous suspensions with various compositions.

Effects of interactions between natural organic matter and aquatic organism degradation products on the transformation and dissolution of cobalt and nickel-based nanoparticles in synthetic freshwater

Expanding applications and production of engineered nanoparticles lead to an increased risk for their environmental dispersion. Systematic knowledge of surface transformation and dissolution of nanoparticles is essential for risk assessment and regulation establishment. Such aspects of Co- and Ni-based nanoparticles including metals, oxides, and solution combustion synthesized metal nanoparticles (metal cores with carbon shells) were investigated upon environmental interaction with organic matter, simulated by natural organic matter (NOM) and degradation products from zooplankton and algae (eco-corona biomolecules, EC) in freshwater (FW). The presence of NOM and EC in FW results in negative surface charges of the nanoparticles reduces the extent of nanoparticles agglomeration, and increases concentration, mainly due to the surface adsorption of carboxylate groups of the organic matter. The dissolution of the Co-based nanoparticles was for all conditions (FW, FW with NOM or EC) higher than the Ni-based, except for Co3O4 being nearly non-soluble. The surface transformation and dissolution of nanoparticles are highly exposure and time-dependent, and surface- and environment specific. Therefore, no general correlation was observed between dissolution and, particle types, surface conditions, or EC/NOM adsorption. This underlines the importance of thorough investigations of nanoparticles adsorption/desorption, degradation, and exposure scenarios for developing regulatory relevant protocols and guidelines.

A new type of silica-induced “moundless” pitting corrosion in copper observed in Japan

A new type of pitting corrosion in copper, namely “moundless” corrosion, has recently been reported in Japan. This type of pitting corrosion has some unique morphological features that differ from ordinary types of pitting corrosion, such as type I or type II. Firstly, this type of pitting corrosion has no mound of corrosion products that cover the mouth of the pit. In addition, a glassy verdigris exists around the pit. Furthermore, the pit measures <1 mm in diameter, but is extremely deep. In our study, we reproduced moundless pits by field testing in an area where moundless pits have often occurred. Moundless pits were also generated in synthetic freshwater through the dissolution of some selected components in a laboratory test. This synthetic freshwater contained 40 ppm SiO2, 50 ppm SO42−, 10 ppm Cl−, and 10 ppm HCO3−. Surface analysis of the moundless pit revealed that the mouths of the pits were covered with thin films that were mainly composed of silica.

Kinetics and mechanisms of flumequine degradation by sulfate radical based AOP in different water samples containing inorganic anions.

Many studies have reported that hydroxyl radical (HO˙) driven advanced oxidation processes (AOPs) could degrade fluoroquinolones (FQs) antibiotics effectively. Compared with HO˙, sulfate radical (SO4˙−) shows a similar oxidation capacity but a longer half-life. SO4˙− could cause chain reactions and resulted in the generation of halogen radicals and carbonate radicals from the main anions in sea water including Cl−, Br− and HCO3−. However, few studies were focused on the degradation of FQs in marine aquaculture water and seawater, as well as the bioaccumulation of transformation products. As a typical member of FQs, flumequine (FLU) was degraded by UV/peroxodisulfate (PDS) AOPs in synthetic fresh water, marine aquaculture water and seawater. The reaction rate constants in the three water samples were 0.0348 min−1, 0.0179 min−1 and 0.0098 min−1, respectively. The reason was attributed to the inhibition of the anions as they could consume SO4˙− and initiate the quenching reaction of free radicals. When the pH value increased from 5 to 9, the reaction rate decreased from 0.0197 min−1 to 0.0066 min−1. The energy difference between HOMO and LUMO of FLU was calculated to be 8.07 eV indicating that FLU was a stable compound. The atoms on quinolone ring of FLU with high negative charge would be more vulnerable to attack by free radicals through electrophilic reactions. Two possible degradation pathways of FLU were inferred according to the degradation products. Preliminary bioaccumulation analysis of transformation products by the EPI suite software proved that the values of log Kow and log BCF of the final product P100 were less than those of FLU and the intermediates.

Influence of natural organic matter on the transformation of metal and metal oxide nanoparticles and their ecotoxic potency in vitro

Increased use and production of engineered nanoparticles (NPs) lead to an elevated risk of their diffuse dispersion into the aquatic environment and increased concern on unknown effects induced by their release into the aquatic ecosystem. An improved understanding of the environmental transformation processes of NPs of various surface characteristics is hence imperative for risk assessment and management. This study presents results on effects of natural organic matter (NOM) on the environmental transformation and dissolution of metal and metal oxide NPs of different surface and solubility properties in synthetic freshwater (FW) with and without NOM. Adsorption of NOM was evident on most of the studied NPs, except Sb and Sb2O3, which resulted in the formation of negatively charged colloids of higher stability and smaller size distribution compared with the same NPs in FW only. The dissolution rate of the NPs in the presence of NOM correlated with the strength of interactions between the carboxylate group of NOM and the particle surface, and resulted in either no (Mn, Sb, ZnO NPs), increased (Co, Sn NPs) and decreased (Ni, NiO, Sb2O3, Y2O3 NPs) levels of dissolution. One type of metal NP from each group (Mn, Ni, Sn) were investigated to assess whether observed differences in adsorption of NOM and dissolution would influence their ecotoxic potency. The results showed Mn, Ni, and Sn NPs to generate intracellular reactive oxygen species (ROS) in a time and dose-dependent manner. The extent of ROS generation in FW was similar for both Mn and Ni NPs but higher for Sn NPs. These findings are possibly related to interactions and infiltration of the NPs with the cells, which lead to redox imbalances which could induce oxidative stress and cell damage. At the same time, the presence of NOM generally reduced the intracellular ROS generation by 20–40% for the investigated NPs and also reduced cytotoxicity of Sn NPs, which can be attributed to the stronger interaction of carboxylate groups of NOM with the surface of the NPs.

Effect of Water Hardness on Catechin and Caffeine Content in Green Tea Infusions.

The health benefits of green tea are associated with its high catechin content. In scientific studies, green tea is often prepared with deionized water. However, casual consumers will simply use their local tap water, which differs in alkalinity and mineral content depending on the region. To assess the effect of water hardness on catechin and caffeine content, green tea infusions were prepared with synthetic freshwater in five different hardness levels, a sodium bicarbonate solution, a mineral salt solution, and deionized water. HPLC analysis was performed with a superficially porous pentafluorophenyl column. As water hardness increased, total catechin yield decreased. This was mostly due to the autoxidation of epigallocatechin (EGC) and epigallocatechin gallate (EGCG). Epicatechin (EC), epicatechin gallate (ECG), and caffeine showed greater chemical stability. Autoxidation was promoted by alkaline conditions and resulted in the browning of the green tea infusions. High levels of alkaline sodium bicarbonate found in hard water can render some tap waters unsuitable for green tea preparation.

Corrosion and transformation of solution combustion synthesized Co, Ni and CoNi nanoparticles in synthetic freshwater with and without natural organic matter

Pure metallic Co, Ni, and their bimetallic compositions of Co3Ni, CoNi, and CoNi3 nanomaterials were prepared by solution combustion synthesis. Microstructure, phase composition, and crystalline structure of these nanoparticles (NPs) were characterized along with studies of their corrosion and dissolution properties in synthetic freshwater with and without natural organic matter (NOM). The nanomaterials consisted of aggregates of fine NPs (3–30 nm) of almost pure metallic and bimetallic crystal phases with a thin surface oxide covered by a thin carbon shell. The nanomaterials were characterized by BET surface areas ranging from ~ 1 to 8 m2/g for the Ni and Co NPs, to 22.93 m2/g, 14.86 m2/g, and 10.53 m2/g for the Co3Ni, CoNi, CoNi3 NPs, respectively. More Co and Ni were released from the bimetallic NPs compared with the pure metals although their corrosion current densities were lower. In contrast to findings for the pure metal NPs, the presence of NOM increased the release of Co and Ni from the bimetallic NPs in freshwater compared to freshwater only even though its presence reduced the corrosion rate (current density). It was shown that the properties of the bimetallic nanomaterials were influenced by multiple factors such as their composition, including carbon shell, type of surface oxides, and the entropy of mixing.

Interaction of metal oxide nanoparticles with microplastics: Impact of weathering under riverine conditions

The ubiquitous distribution of microplastics (MPs) leads to inevitable interactions with the toxic pollutants present in the environment including metal-oxide nanoparticles. This study investigates the interaction of CeO2 nanoparticles (CeNPs) with MPs generated from a disposable plastic container. Further, rough MPs (R-MPs), generated through mechanical abrasion of MPs with sand, were used to probe the impact of roughness. To understand the sorption kinetics and underlying interaction processes, batch experiments were carried out. The results distinctly indicate that CeNPs sorption occurred on MPs surfaces and was consistent with the pseudo-second order kinetics model. For pristine MPs, the sorption capacity was as high as 12.9 mg/g while for R-MPs kinetic equilibrium was achieved faster and an enhanced sorption capacity (13.4 mg/g) was identified. A rise in sorption with an increase in salinity was noted while pH and humic acid exhibited a negative correlation. The observed interactions were attributed to the aggregation profile and surface charge of CeNPs and MPs. Surprisingly, CeNPs also got loaded onto MPs in non-agitated and undisturbed conditions. The sorption process was influenced by the type of aqueous matrix and the sorption capacity at equilibrium followed the trend: distilled water> synthetic freshwater> river water. FTIR spectra, zeta potential, SEM imaging, and elemental mapping revealed electrostatic interaction as the dominant mechanism. This work contributes towards the knowledge gap on the environmental risk of MPs.

Application of Zn/Al layered double hydroxides for the removal of nano-scale plastic debris from aqueous systems

Nano-scale plastic debris (NPDs) are emerging as potential contaminants as they can be easily ingested by aquatic organisms and carry many pollutants in the environment. This study is aimed to remove NPDs from aqueous environment for the first time by using eco-friendly adsorption techniques. Initially, the interaction between NPDs and synthesized Zn-Al layered double hydroxide (LDH) was confirmed by pH titration of Zn-Al LDH against NPDs at varying mass ratio (50:1 to 50:7) and FTIR analysis for both before and after 2 h of contact time. Fast removal was observed in deionized water and synthetic freshwater with maximum sorption capacity (Qmax) of 164.49 mg/g,162.62 mg/g, respectively, according to Sips isotherm. Whereas, removal was least in synthetic hard water having a Qmax value of 53 mg/g. For 2 mM concentration of SO42− and PO43-, the adsorption capacity significantly decreased to 2%. The removal efficiency was found 100 % at pH 4, while at pH 9, it reached 37 % due to increased competitive binding and destabilization of LDH under alkaline conditions. The process of sorption was spontaneous in different types of water studied. The study reveals that Zn-Al LDH can be used as potential adsorbent for the removal of NPDs from freshwater systems.

Ultrasensitive Detection of Nitrite through Implementation of N-(1-Naphthyl)ethylenediamine-Grafted Cellulose into a Paper-Based Device.

Reported herein is the immobilization of N-(1-naphthyl)ethylenediamine (NED) on cellulose via an epichlorohydrin (ECH)-based covalent attachment and the implementation of the functionalized cellulose into an ultrasensitive, paper-based device for nitrite detection. The reported functionalization procedure resulted in a 12.9-fold higher functionalization density than the density that results from the previously reported procedures, and the subsequent device allows for nitrite detection limits in synthetic freshwater and real seawater of 0.26 and 0.22 μM, respectively. The sensor is efficient in a wide range of temperature, humidity, turbidity, and salinity conditions and has been successfully applied for nitrite detection in real water samples.

Corrosion of carbon steel in synthetic freshwater for water distribution systems

Corrosion is one of the most common problems in water distribution systems. The purpose of this research is to investigate the corrosion rate of carbon steel in synthetic freshwater. The influence of a variety of time exposure that represents the actual conditions in practice was performed. Research conducted by weight loss methods using immersion test. The parameters of water quality were measured by using a multimeter portable (Hach HQ40d). From the experiments obtained that the corrosion rate of carbon steel in freshwater ranged between 0.41 - 0.76 mpy. The results of this study are expected as a first step, as input for prevention, to prevent leakage flow and pipe due to corrosion by the life that has been designed.

Biotoxicity of TiO₂ Nanoparticles on Raphidocelis subcapitata Microalgae Exemplified by Membrane Deformation.

TiO2 nanoparticles (NPs), which are mainly used in consumer products (mostly cosmetics), have been found to cause ecotoxic effects in the aquatic environment. The green algae Raphidocelis subcapitata, as a representative of primary producers of the freshwater ecosystem, has been frequently used to study the effects of metal oxide NPs. An ecotoxicity study was conducted herein to investigate the effects of TiO2 NPs on survival and membrane deformation of algal cells. Five different concentrations of nano-TiO2 particles (1, 10, 50, 100 and 500 mg/L) were prepared in synthetic surface water samples with five different water quality characteristics (pH 6.4–8.4, hardness 10–320 mg CaCO3/L, ionic strength 0.2–8 mM, and alkalinity 10–245 mg CaCO3/L). Results showed a significant increase in the hydrodynamic diameter of NPs with respect to both NP concentrations and ionic content of the test system. A soft synthetic freshwater system at pH 7.3 ± 0.2 appeared to provide the most effective water type, with more than 95% algal mortality observed at 50, 100 and 500 mg/L NP concentrations. At high exposure concentrations, increased malondialdehyde formations were observed. Moreover, due to membrane deformation, TEM images correlated the uptake of the NPs.

Influence of humic acid and dihydroxy benzoic acid on the agglomeration, adsorption, sedimentation and dissolution of copper, manganese, aluminum and silica nanoparticles - A tentative exposure scenario.

This work focuses on kinetic aspects of stability, mobility, and dissolution of bare Cu, Al and Mn, and SiO2 NPs in synthetic freshwater (FW) with and without the presence of natural organic matter (NOM). This includes elucidation of particle and surface interactions, metal dissolution kinetics, and speciation predictions of released metals in solution. Dihydroxy benzoic acid (DHBA) and humic acid adsorbed rapidly on all metal NPs (<1 min) via multiple surface coordinations, followed in general by rapid agglomeration and concomitant sedimentation for a large fraction of the particles. In contrast, NOM did not induce agglomeration of the SiO2 NPs during the test duration (21 days). DHBA in concentrations of 0.1 and 1 mM was unable to stabilize the metal NPs for time periods longer than 6 h, whereas humic acid, at certain concentrations (20 mg/L) was more efficient (>24 h). The presence of NOM increased the amount of released metals into solution, in particular for Al and Cu, whereas the effect for Mn was minor. At least 10% of the particle mass was dissolved within 24 h and remained in solution for the metal NPs in the presence of NOM. Speciation modeling revealed that released Al and Cu predominantly formed complexes with NOM, whereas less complexation was seen for Mn. The results imply that potentially dispersed NPs of Cu, Al and Mn readily dissolve or sediment close to the source in freshwater of low salinity, whereas SiO2 NPs are more stable and therefore more mobile in solution.

Effect of triclosan exposure on mortality and behavioral changes of Poecilia reticulata and Danio rerio

ABSTRACTTriclosan (TCS), a chemical used for its antibacterial properties, is an ingredient in many detergents, soaps, deodorants, cosmetics, antimicrobial creams, toothpastes, and an additive in various plastics and textiles. The behavioral changes at different TCS concentrations (0.001–0.002–0.005–0.01–0.02–0.05–0.1–0.2–0.5 mg/L) were determined for the each test organisms in the study. The synthetic freshwater has temperature 20 ± 2°C, dissolved oxygen 7.0 ± 2 mg/L, pH 7.0–8.0. All experiments were replicated three times, in 14 h light, 10 h dark incubations, 10 fishes were put to each aquarium. In hourly and daily observations, times of dead and number for Poecilia reticulata, Danio rerio were recorded. Behavioral changes of Poecilia reticulata and Danio rerio were observed, such as fast-moving, uncontrolled swimming, trying to escape out of the water, vertical action to the water surface, loss of balance, respiratory difficulties, chills, and inversion.

Synthesis of Nitrate Doped Polypyrrole Conducting Polymer Membrane and Fabrication of Passive Sampler to Determine Diffusion of Nitrate and Chloride Through Membrane in Aquatic Ecosystem

Nitrate is the most considerable substance in the hydrosphere and high concentration of nitrate can be harmful to the healthy life of creatures and human being. The removal of nitrate from the water is very essential. Therefore this study was focused to synthesis the nitrate doped polypyrrole polymer membrane (PPy-N) and the diffusion of nitrate in the presence of high chloride concentration through the membrane for samples obtained in 5th, 7th, 9th, 11th, 13th days in synthetic freshwater was also studied. Passive samplers have been developed in order to assess water quality over the period of time they have been deployed and also to simplify sampling and sample preparation processes. Nitrate doped polypyrrole film was synthesized through chemical polymerization process using Pyrrole and HNO3. The characterization of the membrane was performed by Fourier Transform Infrared Spectroscopy (FTIR). The amount of nitrate and chloride diffused through a nitrate doped polypyrrole films (PPy-N1) were determined using cadmium reduction method and chloride ion selective electrode technique respectively. In order to improve the diffusion of nitrate through the membrane, the laboratory filter paper was used to prepare another nitrate doped polypyrrole films (PPy-N2). The same techniques that used for PPy-N1 were used to determine diffused nitrate and chloride through PPy-N2 membrane. The results revealed that, membrane PPy-N2 has exhibited 13.102 ± 0.469 %, 42.969 ± 5.107 %, 55.932 ± 1.579 %, 64.096 ± 2.171 %, and 77.826 ± 1.752 % diffusion of nitrate and 36.989 ± 3.177 %, 43.922 ± 1.823 %, 46.223 ± 0.817 %, 49.042 ± 0.908 %, and 49.679 ± 0.119 % diffusion of chloride through the membrane after 5 days, 7 days, 9 days, 11 days and 13 days respectively. Whereas membrane PPy-N1 exhibited that 11.497 ± 0.715 %, 14.899 ± 1.431 %, 33.932 ± 0.469 %, 35.066 ± 0.592 %, and 42.917 ± 1.875 % diffusion of nitrate and 25.612 ± 1.683 %, 38.959 ± 1.201 %, 36.075 ± 2.151 %, 37.004 ± 2.989 %, and 38.495 ± 1.341 % diffusion of chloride after those days respectively.

Impact of treated wastewater for irrigation on soil microbial communities

The use of treated wastewater (TWW) for irrigation has been suggested as an alternative to use of fresh water because of the increasing scarcity of fresh water in arid and semiarid regions of the world. However, significant barriers exist to widespread adoption due to some potential contaminants that may have adverse effects on soil quality and or public health. In this study, we investigated the abundance and diversity of bacterial communities and the presence of potential pathogenic bacterial sequences in TWW in comparison to synthetic fresh water (SFW) using pyrosequencing. The results were analyzed using UniFrac coupled with principal coordinate analysis (PCoA) to compare diversity and abundance of different bacterial groups in TWW irrigated soils to soils treated with SFW. Shannon diversity index values (H′) suggest that microbial diversity was not significantly different (P<0.086) between soils with TWW and SFW. Pyrosequencing detected sequences of 17 bacterial phyla with Proteobacteria (32.1%) followed by Firmicutes (26.5%) and Actinobacteria (14.3%). Most of the sequences associated with nitrifying bacteria, nitrogen-fixing bacteria, carbon degraders, denitrifying bacteria, potential pathogens, and fecal indicator bacteria were more abundant in TWW than in SFW. Therefore, TWW effluent may contain bacterial that may be very active in many soil functions as well as some potential pathogens.

High Electrical Power Densities from Salinity Gradients By Combining Electrode and Donnan Potentials in a Single Electrochemical Cell

Salinity gradients exist when two waters have different salt concentrations (e.g., when freshwater reaches seawater at coasts or when desalination brine is mixed with less saline water). Salinity gradients contain an immense amount of potential energy, which can theoretically provide 40% of the global electrical demand. One means to harvest salinity gradient energy is to use electrochemical techniques. In an electrochemical cell, a voltage can be created by using salinity gradients to alter electrode potentials in Capacitive Mixing or creating Donnan potentials across ion-exchange membranes in Reverse Electrodialysis. The main challenge with these techniques is that they yield power densities that are too low for commercialization (Capacitive Mixing: ~0.4 W/m2, Reverse Electrodialysis: ~3 W/m2). Here, we combined these two types of potentials in a single electrochemical cell, greatly increasing power densities to values that exceed 12 W/m2 when mixing synthetic freshwater and seawater. We examined how cell design and operating parameters as well as electrode and membrane materials influenced power production and energy efficiency. The results suggest that this type of cell may be used to effectively harvest salinity gradient energy at coasts and produce electricity from saline desalination brines.

Stability of single dispersed silver nanoparticles in natural and synthetic freshwaters: Effects of dissolved oxygen

Silver nanoparticles (AgNPs) are increasingly used in various commercial products. This increased use raises ecological concerns because of the large release of AgNPs into the environment. Once released, the local water chemistry has the potential to influence the environmental fates and behaviors of AgNPs. The impacts of dissolved oxygen and natural organic matter (NOM) on the dissolution and stability of AgNPs were investigated in synthetic and natural freshwaters for 7 days. In synthetic freshwater, the aggregation of AgNPs occurred due to the compression of the electric double layer, accompanied by the dissolution of AgNPs. However, once oxygen was removed, the highest dissolved Ag (Agdis) concentration decreased from 356.5 μg/L to 272.1 μg/L, the pH of the AgNP suspensions increased from less than 7.6 to more than 8.4, and AgNPs were regenerated by the reduction of released Ag+ by citrate. The addition of NOM mitigated aggregation, inhibited oxidative dissolution and induced the transformation of AgNPs into Ag2S due to the formation of NOM-adsorbed layers, the reduction of Ag+ by NOM, and the high affinity of sulfur-enriched species in NOM for Ag. Likewise, in oxygen-depleted natural freshwaters, the inhibition of oxidative dissolution was obtained in comparison with oxygenated freshwaters, showing a decrease in the maximum Agdis concentration from 137.6 and 57.0 μg/L to 83.3 and 42.4 μg/L from two natural freshwater sites. Our results suggested that aggregation and dissolution of AgNPs in aquatic environments depend on the chemical composition, where oxygen-depleted freshwaters more significantly increase the colloidal stability. In comparison with oxic conditions, anoxic conditions were more favorable to the regeneration of AgNPs by reducing species (e.g., citrate and NOM) and enhanced the stability of nanoparticles. This indicates that some AgNPs will be more stable for long periods in oxygen-deprived freshwaters, and pose more serious environmental risks than that in oxygenated freshwaters.