Nanosilver (NAg) is currently one of the major alternative antimicrobials to control microorganisms. With its broad-spectrum efficacy and lucrative commercial values, NAg has been used in medical devices and increasingly, in consumer products and appliances. This widespread use has inevitably led to the release and accumulation of the nanoparticle in water and sediment, in soil and even, wastewater treatment plants (WWTPs). This Article describes the physical and chemical transformations of NAg as well as the impact of the nanoparticle on microbial communities in different environmental settings; how the nanoparticle shifts not only the diversity and abundance of microbes, including those that are important in nitrogen cycles and decomposition of organic matters, but also their associated genes and in turn, the key metabolic processes. Current findings on the microbiological activity of the leached soluble silver, solid silver particulates and their respective transformed products, which underpin the mechanism of the nanoparticle toxicity in environmental microbes, is critically discussed. The Article also addresses the emerging evidence of silver-driven co-selection of antibiotic resistance determinants. The mechanism has been linked to the increasing pools of many antibiotic resistance genes already detected in samples from different environmental settings, which could ultimately find their ways to animals and human. The realized ecological impact of NAg calls for more judicial use of the nanoparticle. The generated knowledge can inform strategies for a better ‘risks versus benefits’ assessment of NAg applications, including the disposal stage.

This study investigates a comparison between the photocatalytic action of two nanocomposites (TiO₂ and TiO₂(Ag) doped) on the degradation of phenol from water. The nanocomposites were synthesized by the UV photo-reduction process to get a silver metal loading of 0.25, 0.5, 0.75, and 1% (w/w). In addition to this, Eriochrome Cyanine Red (ECR) and Eosin Yellow (EY) both anionic dyes were used for sensitization of Ag-doped TiO₂ photo-catalyst such as TiO₂(Ag)ECR and TiO₂(Ag)EY. The TiO₂(Ag-1.0)EY photo-catalyst indicated higher absorbance compared to the TiO₂(Ag-1.0)ECR in the 400–700 nm range (visible range). The degradation of phenol was tested by varying the pH, silver loading and catalyst dosage. The maximum degradation of phenol was 98% in 180 min at pH 7 in presence of 1% (w/w) silver loading with 0.5 gL⁻¹ dosage of photo-catalyst TiO₂(Ag-1.0)EY. At this condition, the reduction in the phenol concentration was noticed from 20 mg/L to 0.4 mg/L.

Metal-based nanoparticles (NPs) are considered detrimental to aquatic organisms due to their potential accumulation. However, little is known about the mechanisms underlying these effects and their species-specificity. Here we used stable silver (Ag) NPs (20 nm, from 10 to 500 μg/L) with a low dissolution rate (≤2.4%) to study the bioaccumulation and biological impacts in two freshwater gastropods: Lymnaea stagnalis and Planorbarius corneus. No mortality was detected during the experiments. Ag bioaccumulation showed a dose-related increase with an enhanced concentration in both species after 7d exposure. L. stagnalis displayed a higher accumulation for AgNPs than P. corneus (e.g., up to 18- and 15-fold in hepatopancreas and hemolymph, respectively) which could be due to the more active L. stagnalis having greater contact with suspended AgNPs. Furthermore, the hepatopancreas and stomach were preferred organs for bioaccumulation compared to the kidney, mantle and foot. Regarding biological responses, the hemolymph rather than hepatopancreas appeared more susceptible to oxidative stress elicited by AgNPs, as shown by significantly increasing lipid peroxidation (i.e., formation of malondialdehyde). Neurotoxicity was detected in L. stagnalis when exposed to high concentrations (500 μg/L). Comparison with impacts elicited by dissolved Ag revealed that the effects observed on AgNPs exposure were mainly attributable to NPs. These results highlighted the relationship between the physiological traits, bioaccumulation, and toxicity responses of these two species to AgNPs and demonstrated the necessity of species-specificity considerations when assessing the toxicity of NPs.

Global plastics production is increasing exponentially and contributing to significant pollution of the marine environment. Of particular concern is ingestion and entanglement risks for marine wildlife, including when items such as rope are incorporated into nest structures. These events are commonly documented using photographic and visual surveys, and each presents a number of challenges and benefits for species conservation and monitoring. Here we compare an invasive (i.e., removing debris from nests) and non-invasive (i.e., photographs) sampling method for quantifying nest debris using the silver gull (Chroicocephalus novahollandiae) as a case study. Overall, 17 debris items were detected in 9% of gull nests. While the use of photographs to monitor nest debris is increasingly popular, the invasive method detected one additional debris item not identified using photography. We therefore recommend caution for nest debris and other monitoring programs where identifying small or cryptic items may require a high level of skill.

Nanoparticles (NP) are potentially reprotoxic, which may compromise the success of populations. However, the reprotoxicity of NP is still scarcely addressed in marine fish. Therefore, we evaluated the impacts of environmentally relevant and supra environmental concentrations of titanium dioxide (TiO₂: 10 to 10,000 μg·L⁻¹) and silver NP (Ag: 0.25 to 250 μg·L⁻¹) on the sperm of gilthead seabream (Sparus aurata). We performed short-term direct exposures (ex vivo) and evaluated sperm motility, head morphometry, mitochondrial function, antioxidant responses and DNA integrity. No alteration in sperm motility (except for supra environmental Ag NP concentration), head morphometry, mitochondrial function, and DNA integrity occurred. However, depletion of all antioxidants occurred after exposure to TiO₂ NP, whereas SOD decreased after exposure to Ag NP (lowest and intermediate concentration). Considering our results, the decrease in antioxidants did not indicate vulnerability towards oxidative stress. TiO₂ NP and Ag NP induced low spermiotoxicity, without proven relevant ecological impacts.

Organic air pollutants represent many different pollutants, including persistent toxic organics and volatile organic compounds (VOC). The VOC group includes about 150 different compounds, the majority of which are considered harmful and toxic to human health. Considering all these features, the removal of VOC is of great importance. According to the Industrial Air Pollution Control Regulation, VOCs in flue gases are classified, and the limit value for the most dangerous group is specified as 20 mg/m³ according to the degree of damage. From past to present, many different removal technologies have been developed and continue to be developed. Removal of pollutants at low concentrations by conventional methods is more inadequate than those above certain concentrations. Photocatalytic oxidation (PCO) is one of the technologies used for VOC removal recently. It has been determined that many different organic pollutants can be removed with this method. Within the scope of this study, the removal of benzene and toluene pollutants, which are two important VOCs frequently encountered in flue gases, by the photocatalytic oxidation method has been studied under UVC irradiation. In this study, a new photocatalyst by doping silver (Ag), a noble metal, and nickel (Ni), one of the transition metals, on TiO₂ nanoparticles was developed and a laboratory-scale reactor system was designed. Many experiments were carried out by changing the system parameters such as ambient temperature (120 °C, 150 °C, 180 °C), humidity (25% and 50%), and percentage of Ag and Ni doping on TiO₂ (0.5%, 1%, 2.5%, %5) and the most successful conditions for the removal of benzene and toluene contaminants were tried to be determined based on the results obtained. When all experiments carried out within the scope of this study were considered, the average removal efficiency for benzene was found as 89.33%, while the average removal efficiency for toluene was 88.23%. According to the obtained results, the most suitable conditions for the simultaneous removal of benzene and toluene pollutants with photocatalytic oxidation method under UVC light were determined as 120 °C temperature, 25% humidity, and 0.5% doping photocatalyst.

Steel is one of the mainly used materials in the oil and gas industry. However, it is susceptible to the marine corrosion, which 20% of the total marine corrosion is caused by microbiologically influenced corrosion (MIC). The economic and environmental impacts of corrosion are significant, and it is crucial to fight against corrosion in a proper sustainability context and environmental-friendly methods. In this study, the graphene oxide/silver nanostructure (GO-Ag) inhibitory effect on the corrosion of steel in the presence of sulfate reducing bacteria (SRB) was investigated, via weight loss (WL) and Tafel polarization measurements. Moreover, molecular dynamic (MD) simulations were performed to obtain a deep understanding of the corrosion inhibition effect of GO-Ag. GO-Ag showed a significant antibacterial effect at 80 ppm. Moreover, WL and Tafel polarization measurements illustrated a great inhibition efficiency, which reached up to 84% reduction of WL and 98% reduction of corrosion current density (Icₒᵣᵣ) after 7 days of incubation with GO-Ag. Based on MD simulations, bonding energy reached to the larger value in the presence of GO-Ag, which indicated the ability of graphene oxide nanosheets to be adsorbed on the steel surface and prevent the access of corrosive agents to the steel surface. The radial distribution function (RDF) results implied distance between corrosive agent (water and SRB) and steel surface (Fe atoms), which indicated protection of the steel surface due to the effective adsorption of GO nanosheets through the active sites of the steel surface. The mean square displacement (MSD) result showed smaller displacement of the corrosive particles on the surface of steel, resulting that the GO-Ag molecules bonded with Fe molecules on the surface of steel.

The use of biochar in soil remediation is a promising method to deal with metal contamination. In the present study, the influence of biochar amendment on the toxicity of silver (as AgNO₃) to terrestrial organisms was assessed. For this, toxicity tests were conducted with terrestrial plant barley (Hordeum vulgare) and invertebrate springtails (Folsomia candida) in the standard natural Lufa soil amended or not with a wood-derived biochar at 5% (w/w). Biochar addition increased root length and mass in barley, compared to unamended soil. However, the effects of Ag on barley growth were masked by a great variation among replicates in biochar-amended soil. Photosynthetic pigment contents (total chlorophyll and carotenoids) were lower in plants exposed to Ag in Lufa soil, but not in biochar-amended soil. Moreover, Ag drastically decreased dehydrogenase activity in Lufa soil. For springtails, the addition of biochar clearly decreased the toxicity of Ag. The LC50 was 320 mg Ag/kg in Lufa soil, while no mortality was observed up to 500 mg Ag/kg in biochar-amended soil. The EC50 for effects on reproduction was significantly higher in biochar-amended soil compared to unamended Lufa soil (315 and 215 mg Ag/kg, respectively). The wood-derived biochar used in this study has shown a potential for remediation of contaminated soils, as a decrease in Ag toxicity was observed in most endpoints analysed in barley and springtails.

The effluents released from textile industries mainly consist of dyes, metals and other pollutants. Dyes often are discharged in wastewater streams causing adverse effect on the environment. To eliminate these harmful dyes, various techniques are emerging out of which nanotechnology is the most reliable and safer. Nanotechnology offers convincing applications in case of environmental and economic concerns. The bio-synthesis of nanoparticles has several advantages over conventional methods and approach towards environment concern as well. Biological method of nanoparticles synthesis is concluded to be the most promising and efficient in action. Bio-synthesised nanoparticles could be used for treatment and decolourisation of dyes in an efficient manner. This review comprises the study of number of bio-synthesised nanoparticles utilised for degradation of various dyes present as pollutants in wastewater. Bio-synthesised nanoparticles such as gold, silver, iron, cobalt, zinc, titanium and molybdenum used for degradation of various dyes have been discussed in this review.

The photocatalytic activity of semiconducting silver carbonate was restricted by the lower stability and fast recombination rate of photogenerated electron–hole pairs. Sulfur-doped graphene oxide (SGO) is used as a cocatalyst for improving the photocatalytic activity of Ag₂CO₃ by reducing the recombination rate. A simple precipitation method was used for the modification of silver carbonate. The chemical, physical, optical, and electrochemical properties of the modified photocatalyst was characterized by XRD, SEM, TEM, UV–vis DRS, XPS, CV, impedance, and amperometry. The fabricated SGO-Ag₂CO₃ composite was successfully degraded various organic pollutants such as methylene blue (MB), rhodamine B(RhB), methyl orange (MO), tartrazine, and thiram with augmented mineralization. The optimization of weight percentage of the developed binary composite with 0.5% SGO-Ag₂CO₃ showed enhanced photocatalytic degradation and followed pseudo-first-order kinetics with rate constant 0.126. More than 90% of degradation efficiency of the pollutants within a short time promises the binary heterostructure for future industrial applications. The excellent stability and reproducibility of the composite opened a new route in the treatment of wastewater.