Silver Nanoparticles In Water Research Articles

Increased Cytotoxicity of Bimetallic Ultrasmall Silver–Platinum Nanoparticles (2 nm) on Cells and Bacteria in Comparison to Silver Nanoparticles of the Same Size

Ultrasmall nanoparticles (diameter 2 nm) of silver, platinum, and bimetallic nanoparticles (molar ratio of Ag:Pt 0:100; 20:80; 50:50; 70:30; 100:0), stabilized by the thiolated ligand glutathione, were prepared and characterized by transmission electron microscopy, differential centrifugal sedimentation, X-ray photoelectron spectroscopy, small-angle X-ray scattering, X-ray powder diffraction, and NMR spectroscopy in aqueous dispersion. Gold nanoparticles of the same size were prepared as control. The particles were fluorescently labeled by conjugation of the dye AlexaFluor-647 via copper-catalyzed azide-alkyne cycloaddition after converting amine groups of glutathione into azide groups. All nanoparticles were well taken up by HeLa cells. The cytotoxicity was assessed with an MTT test on HeLa cells and minimal inhibitory concentration (MIC) tests on the bacteria Escherichia coli and Staphylococcus xylosus. Notably, bimetallic AgPt nanoparticles had a higher cytotoxicity against cells and bacteria than monometallic silver nanoparticles or a physical mixture of silver and platinum nanoparticles. However, the measured release of silver ions from monometallic and bimetallic silver nanoparticles in water was very low despite the ultrasmall size and the associated high specific surface area. This is probably due to the surface protection by a dense layer of thiolated ligand glutathione. Thus, the enhanced cytotoxicity of bimetallic AgPt nanoparticles is caused by the biological environment in cell culture media, together with a polarization of silver by platinum.

Study of Chlorella vulgaris from Different Growth Phases as Biosensor for Detection of Titanium and Silver Nanoparticles in Water

The increased use of metallic nanoparticles has led to concern for environmental contamination and disruption in water quality. Therefore, effective screening of metallic nanoparticles is important for detecting metallic nanoparticles in aquatic environments. Biosensors offer several advantages, including high sensitivity to pollutants, short response time, energy efficiency, and low waste generation. In this study, a whole-cell biosensor was developed using microalga Chlorella vulgaris as a recognition element, and its fluorescence response was used as a measuring parameter for detecting the presence of titanium dioxide (TiO2) and silver (Ag) nanoparticles in water. The responses of C. vulgaris at the lag, exponential, and stationary phases to different concentrations of TiO2 and Ag nanoparticles were studied. The results showed that in TiO2 and Ag nanoparticles exposures, the highest fluorescence change (50-150%) was observed at the lag phase, whereas the lowest fluorescence change (40-75%) was observed at the stationary phase. A significant fluorescence change was observed in 15 min. The immobilized C. vulgaris under TiO2 and Ag nanoparticles exposures showed 30-180% higher fluorescence change than the negative control, indicating the potential of C. vulgaris as a biosensor for rapid detection of TiO2 and Ag nanoparticles in water. The mathematical modeling of the responses of C. vulgaris to TiO2 and Ag nanoparticles at 15 min of exposure with high R2 indicated that this biosensor is sensitive to the concentration tested (0.010–10.000 mg.L-1). Taken together, these results reveal that, for the first time, it is possible to detect TiO2 and Ag nanoparticles in water within a very short time using a microalgae-based biosensor. Moreover, no genetic engineering requirement makes this biosensor simple, economical, and free from the restriction on genetically modified microorganisms for environmental applications.

Refining shape and size of silver nanoparticles using ion irradiation for enhanced and homogeneous SERS activity

We present green synthesis of silver nanoparticles in water using unirradiated and Ag15+\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^{15+}$$\\end{document} ion irradiated phytoextracts of Bergenia Ciliata leaf, Eupatorium adenophorum leaf, Rhododendron arboreum leaf and flower. The use of different plant extracts and their subsequent ion irradiation allow for successful refinement of nanoparticle size and morphology. Due to changes in reducing and capping agents the nanoparticle surface functionalization also varies which not only controls the morphology but also allows for surface oxidation and aggregation processes. In this work, we have synthesized silver nanoparticles which exhibit sizes in the range from 13 to 24 nm and having shapes like spherical, quasispherical, trigonal, hexagonal, cylindrical, dendritic assemblies, and porous nanoparticles. Owing to changes in the size and shape of the nanoparticles, their direct bandgap (2.05 eV - 2.48 eV) and local surface plasmon resonance (420 nm - 490 nm) could also be tuned. These nanoparticles are examined as SERS substrates, where their enhancement factors, limit of detection for methylene blue, and SERS substrate homogeneity have been tested. It has been observed the nanoparticles synthesized using unirradiated plant extracts present an enhancement factor of 106\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^6$$\\end{document} with a limit of detection 10-8\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^{-8}$$\\end{document} M. Whereas nanoparticles with refined morphology and shapes upon irradiation present high enhancement factors of >107\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^7$$\\end{document} and detection limit down to 10-9\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^{-9}$$\\end{document} M. In addition, uniformity in Raman spectra over the SERS substrates has been obtained for selected Ag NPs substrates synthesized using irradiated extracts with minimum relative standard deviation in enhancement factor < 12%.

Human health risk assessment and uncertainty analysis of silver nanoparticles in water.

Despite frequent detection in environmental waters, literature which quantifies the health risk of silver nanoparticles (Ag NPs) through oral ingestion is scarce. This study compiled literature data to find the removal of Ag NPs from different treatment schemes (i.e., natural, engineered, or hybrid). Ag NP concentrations were found either in surface water or in groundwater based on where the effluent of treatment schemes was discharged, i.e.,either in surface water or in groundwater. Monte-Carlo simulation was carried out for probabilistic assessment of health risks for children for two hypothetical exposure scenarios: (a) ingesting river water while swimming and (b) drinking groundwater. Bio-accessible fraction, dietary metal adsorption factor, and concentrations of silver ions were incorporated to simulate realistic situations. Different treatment schemes were ranked for their nanoparticles' removal efficiency with respect to (i) exceedance probability from guideline value and (ii) health risk to children. Hybrid treatment combinations, i.e., conventional primary and secondary treatment units followed by nature-based units (constructed wetlands and soil aquifer treatment), were ranked the best. The health risk value was found to be less than 1, with the 99th percentile value less than 10-3 in all cases. The maximum allowable concentration of Ag NPs was found to be as low as 1.43 mg/L for groundwater, suggesting probable potential for risk. Uncertainty analysis revealed that the uncertainty of the influent NPs concentration in raw wastewater contributes > 99% to the variance of the hazard index. The results of this work indicate that the use of natural treatment technologies with existing engineered treatments provides higher nanoparticle removal from wastewater without the requirement of any tertiary treatment unit.

Highly Selective Colorimetric Sensor of Mercury(II) Ions by Andrographolide-Stabilized Silver Nanoparticles in Water and Antibacterial Evaluation.

Silver nanoparticles (AgNPs) are well known for their exceptional properties and versatility in various applications. This study used andrographolide as a biochemical stabilizer to synthesize AgNPs (andro-AgNPs). The andro-AgNPs were characterized by using UV-vis spectroscopy, revealing a surface plasmon resonance peak at 440 nm. Fourier transform infrared spectroscopy was also used to confirm the presence of AgNPs. Transmission electron microscopy was used to investigate the morphology of andro-AgNPs, which showed a spherical shape with an average diameter of 18.30 ± 5.57 nm (n = 205). Andro-AgNPs were utilized as a colorimetric sensor to detect mercury ions (Hg2+) in water, and the optimized detection conditions were evaluated using UV-vis spectroscopy with a linear range of 15-120 μM. The limit of detection and the limit of quantification for Hg2+ detection were found to be 11.15 and 37.15 μM, respectively. Furthermore, andro-AgNPs exhibited antibacterial properties against both Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria. The results imply that andro-AgNPs hold promising potential for future biomedical applications.

Electrochemical Mechanism of Oxidative Dissolution of Silver Nanoparticles in Water: Effect of Size on Electrode Potential and Solubility.

For the first time, an electrochemical mechanism of oxidative dissolution of silver nanoparticles in aqueous solutions is suggested and substantiated. The dissolution is caused by the occurrence of two interrelated electrochemical processes: (1) silver oxidation on a microanode and (2) oxygen reduction on a microcathode. According to the suggested model, the standard electrode potential of a nanoparticle decreases with a decrease in its size, which leads to an increase in the electromotive force of the oxidative dissolution of silver. A proportional dependence of the solubility of nanoparticles on their standard potential is revealed. An empirical equation is derived that relates the solubility of AgNPs to their electrode potential and size. In the course of oxidation, silver nanoparticles undergo aggregation with a gradual increase in the potential to the value characteristic of the bulk metal. This leads to the deceleration and practical cessation of the dissolution.

Application of textile (PAN-based) activated carbon fibers decorated with silver nanoparticles in water treatment

Introduction: Water treatment deficit and poor health, hygiene and sanitation infrastructure can contribute to disease transmission by dissemination of contaminants and microorganisms. As an alternative, carbon-based materials coated with antimicrobial molecules have been proposed for water treatment, but few supporting data are available so far. Hence, this study investigates the potential use of PAN-based activated carbon fibers (ACF) decorated with silver nanoparticles in water treatment.Methods: Silver nanoparticles were incorporated into the material using a cheap and electroless method. Field emission scanning electron microscopy (FEGSEM), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) characterized the whole material. The textile was mounted on a water filter prototype and had its capacity to remove bacterial (Escherichia coli) and fungal (Candida albicans, Aspergillus niger and Penicillium funiculosum) cells evaluated. Composition and toxicity of the filtered water were determined.Results: Water filtered by Ag@ACF for 2 and 24 h contained 0.254 mg/L and 0.964 mg/L Ag, respectively. Ag@ACF filtering successfully removed E. coli, C. albicans, and A. niger from the suspensions, but not P. funiculosum. Treated water was non-toxic for Vero cells and Drosophila melanogaster, but toxic for Raphidocelis subcapitata. Ag@ACF showed efficient microbial elimination when applied in water treatment. Silver nanoparticles released in aqueous medium may be responsible for R. subcapitata toxicity. Future studies should be conducted to reduce silver nanoparticles release from the carbon fiber.

Space-fractional heat transfer analysis of hybrid nanofluid along a permeable plate considering inclined magnetic field

In this study, the Caputo space-fractional derivatives of energy equation are used to model the heat transfer of hybrid nanofluid flow along a plate. The plate is considered permeable and affected by an inclined magnetic field. We use the space-fractional derivative of Fourier’s law to communicate between the nonlocal temperature gradient and heat flux. The hybrid nanofluid is formed by dispersing graphene oxide and silver nanoparticles in water. The new fractional integro-differential boundary layer equations are reduced to ordinary nonlinear equations utilizing suitable normalizations and solved via a novel semi-analytical approach, namely the optimized collocation method. The results reveal that the increment of the order of space-fractional derivatives and the magnetic inclination angle increase the Nusselt number. Also, an increase in the order of space-fractional derivatives leads to a thicker thermal boundary layer thickness resulting in a higher temperature. It is also found that the temperature of the fluid rises by changing the working fluid from pure water to single nanofluid and hybrid nanofluid, respectively. What is more, the proposed semi-analytical method will be beneficial to future research in fractional boundary layer problems.

200 MeV Ag ion irradiation mediated green synthesis and self assembly of silver nanoparticles into dendrites for enhanced SERS applications

In this paper, we report green and controlled synthesis of silver nanoparticles in water with spherical, hetrogeneously shaped and extended chain like networks using pristine Bergenia ciliata root extracts and the extracts irradiated with Ag15+ swift heavy ion irradiation. The ion fluence on the thin layer of extract modifies the phytomolecules responsible for the reduction and capping of the silver ion and thus changing the morphologies and sizes of the resultant nanoparticles. In addition, the irradiation assists the nanoparticles to agglomerate via surface oxidation providing a core for the growth of dendritic assemblies. Optical, crystallographic and morphological studies reveal surface oxidation of silver nanoparticles is enhanced upon the irradiation of the phytomolecules due to which the surface chemistry of the nanoparticles changes. In addition, these silver nanoparticles and their dendritic assembly exhibit high SERS enhancement factors for methylene blue analyte. The effects of irradiation promote the dendritic assemblies, roughened surfaces over the nanoparticle clusters and hence offer higher enhancement factors as compared to those which have been synthesized using pristine plant extracts.

Tunable wide bandstop and narrow bandpass filters based on one-dimensional ternary photonic crystals comprising defects of silver nanoparticles in water

In this study, we propose a novel structure comprising a one-dimensional photonic crystal of ZnSe/Nb2O5/BK7 as a tunable wide bandstop filter to cover the visible range of 500–800 nm. The transmittance spectrum of the structure was numerically investigated using the transfer matrix method. A stopband covering the range of 609–682 nm was obtained when the structure had nine ternary unit cells. The range widened to cover 576–707 nm when the number of unit cells increased to 20. A narrow bandpass filter was obtained when a defective layer comprising silver nanoparticles dispersed in water was inserted in the middle of the photonic crystal. We demonstrated the tuning of the single bandpass channel by considering the dispersion of the materials due to the modulation of the filling factor and size of the silver nanoparticles as well as the angle of incidence for radiation. The resonant peak with a transmittance of more than 0.85 obtained at normal incidence shifted from 620.8 to 644.5 nm within the bandgap as the filling factor increased from 0.0 to 0.10. We also found that the resonant peak shifted slightly (from 631.5 to 632.4 nm) when the radius of the silver nanoparticles increased from 1.0 to 15.0 nm. In addition, when the angle of incidence increased from 10° to 80°, the resonant peak shifted from 630.0 to 545.8 nm. Therefore, the proposed structure is promising for fabricating practical tunable wide bandstop and single-channel bandpass filters in the visible region.

Femtosecond laser trapping nanoprinting of silver micro/nanostructures

In this paper, silver micro/nanostructures composed of sintered nanoparticles were printed by capturing silver nanoparticles in water with 800 nm femtosecond laser trapping. Relationships of laser power, scanning speed, nanoparticle concentration, and the width and morphology of fabricated silver wire were systematically investigated. It is found that low scanning speed and high nanoparticle concentration favor the printing of silver wire with good morphology. A silver wire with width of 305 nm was printed. Electrical resistivities of printed wires are about 24 times that of bulk silver. Silver grid structures and dot arrays were printed by using this technology. Several three-dimensional silver cuboid structures were also printed. This work provides a protocol for printing of three-dimensional metallic micro/nanostructures using laser trapping. These printed structures have great application prospects in metamaterials, flexible electronics, and SERS.

Green Synthesis of Silver Nanoparticles Using Mukia Maderaspatana

Nanoparticles are utilized in numerous business applications and it has been discovered that watery silver particles can be diminished by fluid exoact of plant parts to deliver exoemely stable silver nanoparticles in water. On this premise, silver nanoparticles (SNPs) were incorporated utilizing leaf aqueoi separate (LAE) of Mukiamaderaspatana. The acquired particles were broke down by UV-obvious spectrophotometry, checking electron microscopy (SEM), Fourier change infrared (FT-lR) spectroscopy to perceive the morphology of AgNPs. FTlR spectroscopic trials hax’e been performed to group potential bioreducing specialists present in the leaves of the plant.

Synthesis of Biocompatible Silver Nanoparticles and Nanotoxicity in Aquatic Ecosystems

ABSTRACTSilver nanoparticles (Ag NPs) have unique optical, electrical, and thermal properties and are being incorporated into products that range from photovoltaics to biological and chemical sensors. The production of silver nanoparticles has been increasing worldwide in the nanotechnology industry due to the variety of applications and are very likely to reach aquatic ecosystems damaging them. Due to their small size and high surface area to volume ratio of NPs, they can strongly interact with life cells and cause damage to tested animals. Based on the mentioned previously, it is necessary to evaluate the silver nanoparticle nanotoxicity in aquatic ecosystems to prevent possible ingestion or transfer to humans. Also, the research will benefit aquatic systems due to less pollution around aquatic organisms. The objectives of this research included: i) production and characterization of stable silver nanoparticles in water, ii) characterizing the optical properties by UV-Vis spectroscopy and morphology by HR-TEM and; iii) evaluate the toxicity of silver nanoparticles in aquatic organisms, i.e Artemia salina. Results obtained evidenced that Ag NPs showed an intense absorption peak at 448 nm. This broad peak is due to the phenomenon called surface plasmon resonance (SPR) that is responsible for a variety of phenomena, including nanoscale optical focusing, negative refraction, and surface-enhanced Raman scattering. HR-TEM measurements evidenced the spherical form of the nanoparticles and its small size at around 12-20 nm. In addition, Electron Diffraction analyses suggested the composition of the nanoparticle, which contained only Ag0. The toxicity assays were evaluated using different concentrations of purified Ag NPs. During the cytotoxicity assay, it was demonstrated that Ag NPs were not toxic to Artemia salina after 24 and 48 hours of exposure. However, silver (as silver nitrate) evidenced high toxicity to Artemia salina at larval stage.

Electrospun Bi-layered Composite Membrane for the Removal of Metallic Contaminants in Drinking Water

Using biodegradable polymer polycaprolactone (PCL) and zeolite, the present experiment was conducted with the aim of using biodegradable PCL and zeolite based composite membrane to remove silver in drinking water. After optimizing the electrospinning parameters, a double-layered PCL and PCL/zeolite electrospun composite membranes were manufactured. The membranes were then characterized using a scanning electron microscope (SEM) and an energy dispersive X-ray (EDX) and the filtration phenomenon was conducted by dispersing silver nanoparticles in water. After comparing the filtration results using an inductively coupled plasma optical emission spectrometry (ICP-OES), it was observed that the bi-layered membrane filtered 90% of silver present in the water. The present work shows that the new PCL/zeolite based double-layered membrane can be promising to remove contaminants in drinking water.

Stabilization of Silver Nanoparticles by Cationic Aminoethyl Methacrylate Copolymers in Aqueous Media-Effects of Component Ratios and Molar Masses of Copolymers.

The ability of aminoethyl methacrylate cationic copolymers to stabilize silver nanoparticles in water was investigated. Sodium borohydride (NaBH4) was employed as a reducing agent for the preparation of silver nanoparticles. The objects were studied by ultraviolet-visible (UV-vis) spectroscopy, dynamic light scattering (DLS), analytical ultracentrifugation (AUC) and scanning electron microscopy (SEM). Formation of nanoparticles in different conditions was investigated by varying ratios between components (silver salt, reducing agent and polymer) and molar masses of copolymers. As a result, we were successful in obtaining nanoparticles with a relatively narrow size distribution that were stable for more than six months. Consistent information on nanoparticle size was obtained. The holding capacity of the copolymer was studied.

From Concentrated Dispersion to Solid β‐Cyclodextrin Polymer‐Capped Silver Nanoparticle Formulation: A Trojan Horse Against Escherichia coli

AbstractPreparation of concentrated silver nanoparticles in water remains a challenge today. The intrinsic reactivity of silver, as well as the high surface energy of nanoparticles, make it difficult to handle them without altering their pristine properties. Herein, we report the preparation of concentrated silver nanoparticles (AgNPs) dispersion (2 mM; 1.5⋅1015 NPs/mL) by reducing Ag+ in‐situ of a β‐cyclodextrin‐epichlorohydrin polymer (βCDP) as a capping agent. The prepared nanoparticles (AgNPs@βCDP) with a Surface Plasmon Resonance band at 396 nm, and a hydrodynamic diameter of 21.4 ±1.8 nm, retained both features after being precipitated and re‐dispersed in water. The AgNPs core had a spherical morphology, with a 12.7 ±1.5 nm diameter in size, as determined by TEM. The AgNPs@βCDP showed outstanding bactericidal properties against Escherichia coli (MIC= 0.37 nM), one of the lowest ever achieved for silver nanoparticles. We suggest that the polymer acts as a Trojan horse with AgNPs as payload.

Laser ablation synthesis of silver nanoparticles in water and dependence on laser nature

Silver nanoparticles have been synthesized by a one step, easy, fast and green method. The nanoparticles were prepared in de-ionized water by laser ablation method using two lasers, a continuous wave (CW) diode laser and a pulsed Nd:YAG laser. The purpose of the experiment is to compare the role of nature of the laser for production of better NPs. The prepared silver nanoparticles were characterized for their, structural, physical and optical properties. The structural properties of the synthesized nanoparticles were characterized by X-ray Diffraction and the nanoparticles were found to be crystalline. The physical properties were analyzed by Atomic Force Microscopy which confirmed spherical and nanometer sized nanoparticles. The average size was 20 nm and 9 nm for continuous and pulsed laser respectively. The optical properties were analyzed by UV–Visible spectroscopy where band gap energy was investigated and increase in band gap energy as compared to bulk was observed. The green nature of laser ablation method, surface chemistry and chemical contamination of the surface of prepared nanoparticles were analyzed by Fourier Transform Infrared Spectroscopy. The thermal conductivity of the nanoparticles colloidal solutions (nanofluids) was calculated and an enhancement of 16% and 27% was observed for CW and pulsed laser prepared nanofluids respectively as compared to base liquid (de-ionized water).

Stabilization of Silver Nanoparticles in Water with a Cationic Copolymer Based on Poly(Aminoethyl Methacrylate)

It has been shown that a cationic copolymer based on poly(aminoethyl methacrylate) is capable of stabilizing silver nanoparticle dispersions in aqueous media. Nanoparticles have been prepared via chemical reduction of AgNO3 in an aqueous solution with sodium borohydride in the presence of a cationic random terpolymer—poly(2-aminoethyl methacrylate-co-N-methyl-2-aminoethyl methacrylate-co-N,N-dimethyl-2-aminoethyl methacrylate). Spectrophotometry has been employed to show that silver dispersions formed in the presence of the copolymer are stable for a long time (more than half a year). Using dynamic light scattering and scanning electron microscopy, consistent information has been obtained on the sizes and size distribution of the stabilized nanoparticles.

Biogenic Synthesis of Silver Nanoparticle from Mushroom Exopolysaccharides and its Potentials in Water Purification

Objective:This study reports a novel eco-friendly biosynthesis of Silver Nanoparticles (AgNPs) from Exopolysaccharides (EPS) ofLentinus edodesafter an attempt to optimise the production of EPS through mutagenesis. It further describes some potential application of silver nanoparticles in water treatment.Methods:A wild strain ofL. edodeswas subjected to UV irradiation, a physical mutagen, at 254 nm. The wild and resultant irradiated strains were then assessed for the production of EPS and subsequent application of the crude EPSs for biosynthesis of AgNPs. The particles were characterised by colour pattern and UV-visible spectroscopy. Based on superior EPS production and nanoparticle attributes, nanoparticles obtained from UV irradiated process were further subjected to Scanning Electron Microscopy (SEM). EPS produced was quantified by the phenol-sulphuric acid method and studied by GC-MS.Results:Results obtained for EPS productivity indicated the presence of monomer sugars such as arabinose (50.65%), mannose (19.20%), mannitol (15.58%), fructose (7.96%), trehalose (6.49%), and glucuronic acid, xylose, galactose and glucose with low percentages of ≤ 0.11. EPS productivity of wild and mutant strains was obtained as 1.044 and 2.783 mg/ml, respectively, after 7 days of fermentation. The result of EPS production for UV irradiated strain corresponds to a yield improvement of 2.7 fold of the wild-type. UV Spectroscopy and SEM analysis studies on EPS nanoparticle product of the improved (UV irradiated) strain indicated the formation of AgNPs at the absorption band of 421 nm with a size range of 50-100 nm.Conclusion:This study, which aimed at eco-friendly synthesis of myco-nanoparticle has established the novel ability ofL. edodes’polysaccharide in silver nanoparticles biosynthesis. It expounded potential frontiers of silver nanoparticles application in the water industry. To the best of the authors’ knowledge, this result represents the first report on the biosynthesis of AgNPs usingL. edode’sEPS.

Detection of suspended nanoparticles with near-ambient pressure x-ray photoelectron spectroscopy

Two systems of suspended nanoparticles have been studied with near-ambient pressure x-ray photoelectron spectroscopy: silver nanoparticles in water and strontium fluoride—calcium fluoride core-shell nanoparticles in ethylene glycol. The corresponding dry samples were measured under ultra high vacuum for comparison. The results obtained under near-ambient pressure were overall comparable to those obtained under ultra high vacuum, although measuring silver nanoparticles in water requires a high pass energy and a long acquisition time. A shift towards higher binding energies was found for the silver nanoparticles in aqueous suspension compared to the corresponding dry sample, which can be assigned to a change of surface potential at the water-nanoparticle interface. The shell-thickness of the core-shell nanoparticles was estimated based on simulated spectra from the National Institute of Standards and Technology database for simulation of electron spectra for surface analysis. With the instrumental set-up presented in this paper, nanoparticle suspensions in a suitable container can be directly inserted into the analysis chamber and measured without prior sample preparation.