Conventional remediation techniques have become outdated and insufficient to treat the influx of pollution from different fronts (air, water, and soil). Green synthesis of nanoparticles is an eco-friendly approach to remediate these contaminants and Membrane technology is increasingly becoming popular for the treatment of wastewater due to their efficiency and versatility against a wide array of contaminants. Cellulose acetate (CA) is a polymer obtained from cellulose and hence considered biodegradable, making it a more environmentally friendly option over other conventional polymers. In this present study, silver nanoparticles were synthesized using Staphylococcus aureus and characterized by UV-vis Spectrometer, Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Analysis (EDAX). The synthesized green silver nanoparticles were assimilated onto synthesized CA membrane films to fabricate nanocomposite membranes (CA-X, CA-X1 and CA-X2). EDAX results showed higher counts of silver at 3keV on the CA-X, confirming that silver nanoparticles were properly embedded on the membrane. Physio-chemical tests performed on the collected sewage, showed that the total dissolved solids (TDS) were found to decrease significantly during the first hour of treatment, CA-X1 showed 16.2% decrease and 21.95% decrease was observed by CA-X2. A decrease in total nitrogen content by 38.88% and 41.36% for CA-X1 and CA-X2 respectively was recorded after a week’s treatment. Therefore, the work displayed the capability of cellulose acetate nanocomposite membrane for leachate treatment, since it displayed its potential in remediating leachate in a short span of time and scalability could be achieved for a larger volume of leachate with larger nanocomposite membranes.

This work explores the synthesis and characterization of two novel nanocomposites that can be used in various applications, such as aqueous solution adsorption of pollutants. The first nanocomposite consists of tin (Sn)-doped titanium dioxide (TiO2) on activated carbon, while the other one consists of polypyrole (PPy), chitosan (CS), and Sn-doped TiO2. A contrast was made of their effective adsorbent materials for the removal of Cibacron Brilliant Yellow dye from aqueous solutions. Different analytical techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), energy dispersive X-ray analysis (EDX), and Fourier transform - infrared (FT-IR) were used to analysis the nanocomposite samples. SEM images show that the average particle diameter of PPy-CS/Sn-doped TiO2 NC is 75 ± 3 nm, while Sn-doped TiO2/AC particles have an average diameter of 40 ± 2 nm. The greater PPy-CS/Sn-doped TiO2 nanocoposite particle diameter indicates that the polymers cover the Sn-doped TiO2 nanoparticles, which leads to higher in the diameter of the particles. The adsorption efficiency of Sn-doped TiO2/AC was higher than that of PPy-CS/Sn-doped TiO2 sample due to its smaller particle size which resulted in a higher surface area which provides more adsorption sites. However, both samples showed remarkable adsorption capacity, where the adsorption capacity of Sn-doped TiO2/AC and PPy-CS/Sn-doped TiO2 were 104 and 103 mg/g, respectively.

Increasing the pollution rate of water sources is one of the most severe issues that the world faces. This issue has stimulated researchers to investigate different treatment methods such as adsorption, chemical precipitation, membrane filtration, flocculation, ion exchange, flotation, and electrochemical methods. Among them, adsorption has gained broad interest due to its ease of operation, low cost, and high efficiency. The critical factor of the successful adsorption treatment process is finding attractive adsorbents with attractive criteria such as low cost and high adsorption capacity. In the last few decades, nanotechnology has attracted much attention, and numerous nanomaterials have been synthesized for water and wastewater treatment. This work provides a quick overview of nanomaterials, which have been investigated for water remediation as adsorbent and photocatalyst. This work reviewed more than 100 articles to provide a critical review that would determine the limitation of using nanomaterials in water treatment at the commercial scale.

The present study prepares alkali lignin (AL) via acidification of black liquor, obtained from a pulp and paper factory. The average molecular weight of AL (equal to 2,530 g/mol) has been determined with gel permeation chromatography. AL has been modified by ethylene glycol, while lignin nanoparticles (LN) has been prepared through acid precipitation technology, their size being assessed by means of DLS to show that the average diameter of the nanoparticles at pH = 4 has been 52.7 nm. Afterwards, it has used AL and LN to remove Basic Red 2 (BR2) from aqueous solutions. The absorbent structures and morphologies of AL and LN have been investigated using SEM, and FT-IR spectroscopy. The optimal conditions for the absorption of AL and LN, using 0.1 gr of the absorbent, include 100 min of duration, at pH of 7, and an initial dye concentration amounting to 100 mg/L. Furthermore, the absorption amount has been mathematically described as a function of experimental parameters, modeled by means of Response Surface Methodology (RSM). A central composite design (CCD) has been applied to evaluate the impacts of four independent variables. Optimum absorption values, obtained via empirical methods, completely match with the values, calculated by the program called Design-Expert. Both absorbent AL and LN show agree with Langmuir Isotherm with maximum absorption capacities of AL and LN being 55.2 mg/gr and 81.9 mg/gr, respectively. The experimental results show that both absorbent LN and AL follow both pseudo-second kinetic and the intraparticle diffusion models.

The study investigates the effect of aluminium oxide nanoparticles as an additive to Madhuca Indica (mahua) methyl ester blends on performance, emission analysis of a single-cylinder direct injection diesel engine operated at a constant speed at different operating conditions. The test fuels are indicated as B10A0.2, B10A0.4, B20A0.2, B20A0.4 and diesel respectively. The results indicate that the brake thermal efficiency for aluminium oxide nanoparticles blended biodiesel increases slightly when compared to the mineral diesel. The carbon monoxide (CO), unburnt hydrocarbon (HC) and smoke emission marginally decrease as compared to mineral diesel. Oxides of nitrogen (NOx) emissions are minimum for the aluminium oxide nanoparticles blended mahua methyl esters. Higher cylinder gas pressure and heat release rate were observed for aluminium oxide nanoparticles blended mahua methyl ester. From the study, the blending of aluminium oxide nanoparticles in biodiesel blends produces a most promising results in engine performance and also reduces the harmful emission from the engines.

peer reviewed | Copper and zinc are metals that have been traditionally thought of as past contamination legacies. However, their industrial use is still extensive and current applications (e.g. nanoparticles and antifouling paints) have become additional marine environment delivery routes. Determining a pollutant's genotoxicity is an ecotoxicological priority, but in marine benthic systems putative substances responsible for sediment genotoxicity have rarely been identified. Studies that use sediment as the delivery matrix combined with exposures over life-history relevant timescales are also missing for metals. Here we assess copper and zinc's genotoxicity by exposing the ecologically important polychaete Alitta virens to sediment spiked with environmentally relevant concentrations for 9 months. Target bioavailable sediment and subsequent porewater concentrations reflect the global contamination range for coasts, whilst tissue concentrations, although elevated, were comparable with other polychaetes. Survival generally reduced as concentrations increased, but monthly analyses show that growth was not significantly different between treatments. The differential treatment mortality may have enabled the surviving worms in the high concentration treatments to capture more food thus removing any concentration treatment effects for biomass. Using the alkaline comet assay we confirm that both metals via the sediment are genotoxic at concentrations routinely found in coastal regions and this is supported by elevated DNA damage in worms from field sites. However, combined with the growth data it also highlights the tolerance of A. virens to DNA damage. Finally, using long term (decadal) monitoring data we show stable or increasing sediment concentrations of these metals for many areas. This will potentially mean coastal sediment is a significant mutagenic hazard to the benthic community for decades to come. An urgent reappraisal of the current input sources for these ‘old pollutants’ is, therefore, required. Chronic exposure of zinc and copper via sediment at environmentally relevant concentrations induces DNA damage in a marine polychaete. © 2018 Elsevier Ltd

International audience | The ability of metallic nanoparticles to be oxidized, reduced or dissolved in biological media can be used to predict their toxicity in vitro. a b s t r a c t The level of production of nanoparticles will inevitably lead to their appearance in air, water, soils, and organisms. A theoretical framework that relates properties of nanoparticles to their biological effects is needed to identify possible risks to human health and the environment. This paper considers the properties of dispersed metallic nanoparticles and highlights the relationship between the chemical stability of these nanoparticles and their in vitro toxicity. Analysis of published data suggests that chemically stable metallic nanoparticles have no significant cellular toxicity, whereas nanoparticles able to be oxidized, reduced or dissolved are cytotoxic and even genotoxic for cellular organisms.

To evaluate the influence of surface coatings on nano-fertilizers uptake and their phytotoxicity to crops and its health risk to Chinese adults, trisodium citrate (TC) and polyethylene glycol (PEG) coatings were prepared on the surface of copper oxide nanoparticles (CuO NPs), respectively, with 100 and 500 mg/L of bare CuO NPs, TC-CuO NPs, and PEG-CuO NPs were exposed to soil-grown Ipomoea aquatica Forssk. Combined bio-transmission electron microscopy and micro-CT observed cellular migration of coated CuO NPs in symplastic and apoplastic pathways, as well as nanoparticles transported through vascular tissues to the above-ground parts. Since TC-CuO NPs had less inhibition on vascular phylogeny of I. aquatica roots which was determined by RT-qPCR, their migration in plants was more efficient, thus exhibiting greater phytotoxicity to shoots. Meanwhile, coatings significantly reduced the phytotoxicity of CuO NPs by stimulating plant antioxidant defense. The risk of CuO nano-fertilizers on human dietary safety was evaluated, the HQ > 1 in the 500 mg/L CuO NPs treatment indicated a potential health risk to Chinese adults, which was reduced by the coatings. This work explored for the first time the mechanism of coating effects on nanoparticles migration efficiency and phytotoxicity at the molecular level and demonstrated that the migration of nanoparticles between tissues could have an impact on phytotoxicity. It implied that coating can be tailored to target nanoparticles to specific regions of the plant. In addition, this study highlights the potential health risks associated with the consumption of I. aquatica fertilized with CuO NPs and provides valuable insights into the environmental applications of nano-fertilizers.

The excessive arsenic (As) accumulation in plant tissues enforced toxic impacts on growth indices. So, the utilization of As-contaminated food leads to risks associated with human health. For the reduction of As concentrations in foods, it is obligatory to fully apprehend the take up, accretion, transportation and toxicity mechanisms of As within plant parts. This metalloid impairs the plant functions by disturbing the metabolic pathways at physio-biochemical, cellular and molecular levels. Though several approaches were utilized to reduce the As-accumulation and toxicity in soil-plant systems. Recently, engineered nanoparticles (ENPs) such a zinc oxide (ZnO), silicon dioxide or silica (SiO₂), iron oxide (FeO) and copper oxide (CuO) have emerged new technology to reduce the As-accumulation or phytotoxicity. But, the mechanistic approaches with systematic explanation are missing. By knowing these facts, our prime focus was to disclose the mechanisms behind the As toxicity and its mitigation by ENPs in higher plants. ENPs relives As toxicity and its oxidative damages by regulating the transporter or defense genes, modifying the cell wall composition, stimulating the antioxidants defense, phytochelatins biosynthesis, nutrients uptake, regulating the metabolic processes, growth improvement, and thus reduction in As-accumulation or toxicity. Yet, As-detoxification by ENPs depends upon the type and dose of ENPs or As, exposure method, plant species and experimental conditions. We have discussed the recent advances and highlight the knowledge or research gaps in earlier studies along with recommendations. This review may help scientific community to develop strategies such as applications of nano-based fertilizers to limit the As-accumulation and toxicity, thus healthy food production. These outcomes may govern sustainable application of ENPs in agriculture.

Titanium dioxide nanoparticles (TiO₂ NPs) easily combine with other pollutants such as heavy metals because of their excellent physiochemical properties. However, how such an interaction may affect the binding behavior of metals onto biofilms remains largely unclear. This study, examined the effects of TiO₂ NPs on Cd²⁺ accumulation and toxicity for natural periphytic biofilms were examined. The adsorption kinetics showed that adding 0.1 and 1 mg/L TiO₂–NPs increased the Cd²⁺ adsorption of biofilms at equilibrium by 23.5% and 35.8%, respectively. However, adding 10 mg/L TiO₂ NPs increased the Cd²⁺ adsorption of biofilms at equilibrium by only 1.9%. The adsorption isotherms indicate that the presence of TiO₂ NPs considerably increased the Cd²⁺ adsorption capacity of the biofilms; however, this effect became less prominent at high TiO₂ NP concentrations. The optimum pH for Cd²⁺ adsorption increased with increasing Cd²⁺ and TiO₂ NP contents. At low concentrations, the coexistence of Cd²⁺ and TiO₂ NPs may facilitate their respective accumulation by stimulating the secretion of extracellular polymeric substances and enhancing the microbial activity of the biofilm. The presence of TiO₂ NPs increases the surface binding energy between Cd²⁺ and functional groups such as carboxyl groups, enhancing the Cd²⁺ accumulation on the biofilm.