Ultrasound Irradiation Coating of Silver Nanoparticle on ABS Sheet Surface

Ultrasound irradiation was used for anchoring silver nanoparticles with an average size from 10 to 50 nm onto the surface of acrylonitrile–butadiene–styrene (ABS) sheets 1 mm thick. The sonochemical reduction was carried out under argon at room temperature. Silver nanoparticles were obtained and deposited on the ABS surface by the irradiation of a mixture containing ABS plaques, silver nitrate (AgNO₃), ethylene glycol and water. Reaction conditions such as temperature, AgNO₃ concentration and irradiation time were controlled to achieve the deposition of silver nanoparticles onto the surface of ABS sheets. Nano silver coated ABS samples were characterized by X-ray diffraction, transmission and scanning electron microscopy, Raman spectroscopy and antimicrobial activity, specifically against the fungus, Aspergillius niger, and the bacterium, Escherichia coli. The observed results may be applied in the design of industrial ABS sheets with antimicrobial characteristics.     

Preparation of silver hydrosols using polyethylene glycol modified with vinyl pyrrolidone

Hydrosols containing silver nanoparticles were prepared from copolymers of ethylene glycol (EG) and vinyl pyrrolidone (VPy). The copolymers were synthesized using a macro-azo-radical initiator appended with EG units. The hydrosols were prepared by simply stirring the copolymers with AgNO₃ in water at room temperature. The nanoparticles conferred thermal stability to the hydrosols, up to 80 °C. Spectroscopic, thermal, and gas chromatography analyses revealed that the silver nanoparticles were protected by EG and carbonyl groups with strong interaction between silver and the oxygen species of EG and VPy.     

Formation of a liquid film of AgNO3 on a silver surface

The behavior of a AgNO₃/Ag₂O/Ag “sandwich” upon heating in vacuum was studied by in situ X‐ray photoelectron spectroscopy (XPS) and ex situ scanning electron microscopy (SEM). The AgNO₃/Ag₂O/Ag “sandwich” was prepared by exposure of a silver foil to a NO : O₂ mixture. The upper layer of the “sandwich” consists of AgNO₃ crystals of a mean size between 0.1 and 0.4 μm. Heating at 550 K in vacuum results in melting of the AgNO₃ crystals. A liquid film of AgNO₃, readily wetting the silver, covers the surface. Cooling below the melting point of AgNO₃ leads to the agglomeration of silver nitrate to long islands with a size reaching a few tens of micrometers (μm). The possible effects of AgNO₃ liquid‐phase formation on surface processes are discussed. This revised version was published online in July 2006 with corrections to the Cover Date.     

Synthesis of silver particles below 10 nm using spinning disk reactor

Silver nanoparticles were synthesized via a reduction reaction carried out in a spinning disk reactor, to which an AgNO₃ solution containing a protecting agent and an alkaline solution containing a reducing agent were added simultaneously and then recycled for a certain period. Besides starch, which has been used for producing silver particles above 10 nm, two more protecting agents, i.e. polyvinyl pyrrolidone (PVP) and hydroxypropyl methyl cellulose (HPMC), were tested in order to prepare silver particles below 10 nm. Then, the effects of other operating variables, such as rotation speed of disk, flow rates of reactant streams, concentration of reducing agent, and type and concentration of alkali, were investigated, aiming at a high production rate of silver nanoparticles with a size below 10 nm. The produced silver particles were recovered using a centrifuge, and the size did not change after redispersion. The sintering temperature of the 10 nm silver particles was greatly reduced.     

Preparation and Characterization of Gelatin Nanofibers Containing Silver Nanoparticles

Ag nanoparticles (NPs) were synthesized in formic acid aqueous solutions through chemical reduction. Formic acid was used for a reducing agent of Ag precursor and solvent of gelatin. Silver acetate, silver tetrafluoroborate, silver nitrate, and silver phosphate were used as Ag precursors. Ag⁺ ions were reduced into Ag NPs by formic acid. The formation of Ag NPs was characterized by a UV-Vis spectrophotometer. Ag NPs were quickly generated within a few minutes in silver nitrate (AgNO₃)/formic acid solution. As the water content of formic acid aqueous solution increased, more Ag NPs were generated, at a higher rate and with greater size. When gelatin was added to the AgNO₃/formic acid solution, the Ag NPs were stabilized, resulting in smaller particles. Moreover, gelatin limits further aggregation of Ag NPs, which were effectively dispersed in solution. The amount of Ag NPs formed increased with increasing concentration of AgNO₃ and aging time. Gelatin nanofibers containing Ag NPs were fabricated by electrospinning. The average diameters of gelatin nanofibers were 166.52 ± 32.72 nm, but these decreased with the addition of AgNO₃. The average diameters of the Ag NPs in gelatin nanofibers ranged between 13 and 25 nm, which was confirmed by transmission electron microscopy (TEM).     

In vitro efficacy and toxicology evaluation of silver nanoparticle‐loaded gelatin hydrogel pads as antibacterial wound dressings

The silver nanoparticle (nAg)‐loaded gelatin hydrogel pads were prepared from 10 wt % gelatin aqueous solution containing silver nitrate (AgNO₃) at 0.75, 1.0, 1.5, 2.0, or 2.5 wt % by solvent‐casting technique. These AgNO₃‐containing gelatin solutions, that had been aged for 15, 12, 8, 8, and 8 h, respectively, showed noticeable amounts of the as‐formed nAgs, the size of which increased with an increase in the AgNO₃ concentration (i.e., from 7.7 to 10.8 nm, on average). The hydrogels were crosslinked with a glutaraldehyde aqueous solution (50 wt %, at 1 μL mL^?1). At 24 h of submersion in phosphate buffer saline (PBS) or simulated body fluid buffer (SBF) solution, about 40.5–56.4% or 44.4–79.6% of the as‐loaded amounts of silver was released. Based on the colony count method, these nAg‐loaded hydrogels were effective against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, with at least about 99.7% of bacterial growth inhibition. Unless they had been treated with a sodium metabisulfite aqueous solution, these hydrogels were proven, based on the indirect cytotoxicity evaluation, to be toxic to human's normal skin fibroblasts. Lastly, only the hydrogels that contained AgNO₃ at 0.75 and 1.0 wt % were not detrimental to the skin cells that had been cultured directly on them. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Modification of silver iodide particles caused by a flow of electrons

A crystalline powder of AgI has been synthesized using an exchange reaction of aqueous solutions of AgNO₃ and KI. The size and shape of the crystals are determined with the help of scanning electron microscopy. It is shown that nanocrystalline silver particles (30–70 nm) are formed at the surface of monocrystalline AgI particles (500–2000 nm) under the action of a focused bunch of electrons.     

Spectroscopic analysis and catalytic application of biopolymer capped silver nanoparticle,an effective antimicrobial agent

Microbial reduction of silver ion (conc. 1 mM AgNO₃) was performed by Alkaliphilus oremlandii strain ohILAs in an alkaline pH 10. The synthesized silver nanoparticle was stabilized by poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) biopolymer which was also synthesized by the microbial culture of Alkaliphilus oremlandii strain ohILAs at pH8. The particle size and shape of the silver nanoparticles was studied by dynamic light scattering and under a transmission electron microscope and it was found that the particle size of polymer stabilized colloidal silver was comparatively lower (22–43nm) than that for the unstabilized one (63–93 nm). The stabilization of nanoparticles in polymer dispersed medium after around 60 days was confirmed from analysis of UV‐visible spectroscopy and scanning electron microscopy. The crystalline peaks as recorded with X‐ray's diffraction were observed at 2θ values of 38° and 43°, indicating the fcc crystalline structure of the silver nanoparticle. The antimicrobial activity of silver nanoparticles on gram‐negative bacteria strain (Escherichia coli XL1B) and gram‐positive strain (Lysinibacillus fusiformis) showed better performance by the solution of polymer stabilized nanoparticle than that for the non polymer stabilized one. The reduction of nitro group in p‐nitrophenol to p‐aminophenol was observed from the analysis of UV‐Visible spectroscopy in which, the shifting of absorption peak at 400 to 295 nm and the simultaneous regeneration of light brown color (λ_max 410 nm) of silver nanoparticles confirmed the catalytic activity of silver nanomaterials. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41495.     

Preparation and Characterization of Polypyrrole Silver Nanocomposites via Interfacial Polymerization

Conducting polypyrrole silver (Ppy-AgNC) nanocomposite was synthesized by an interfacial polymerization method. Ag⁺ ions from the AgNO₃ solution were taken in the formation of Ppy-AgNC. The incorporated silver was confirmed by X-ray diffraction (XRD). During the polymerization in a nitrate ion-containing solution, the impregnation leads to the formation of metallic silver. The size distribution of Ag into the polymer is confirmed by transmission electron microscopy (TEM), and proves the formation of a uniform species with spherical particles of Ag (mean diameter of 8-12 nm) branching at the border of Ppy. The thermal behavior of the material was studied by thermogravimetric measurements.     

Preparation and characterization of silver nanoparticles with dendrimers as templates

In this study, crystal silver nanoparticle clusters, prepared by the reduction of AgNO₃ in the presence of third-to-sixth-generation dendrimers with a trimesyl core, were characterized with ultraviolet–visible spectroscopy, transmission electron microscopy, and energy-dispersive X-ray spectroscopy. The results showed that the particle size of the silver nanoparticles was considerably affected by the generation of the dendrimers as well as the dendrimer concentration. When the concentration ratios of Ag⁺ to the third-to-sixth-generation dendrimers were all 4 : 1, the average diameters of the obtained particles were 6.7, 6.0, 5.2, and 4.3 nm, respectively. The data from high-resolution transmission electron microscopy and electron diffraction indicated that the particles belonged to a simple cubic crystal structure. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

在NiCl2、MnCl2或FeCl3存在下用多元醇法高浓度合成银纳米线

报道了一种用于高浓度制备银纳米线的改性多元醇法。在NiCl₂、MnCl₂或FeCl₃存在下高浓度地制得了具有均一尺寸和形貌的银纳米线。所得银纳米线的直径约为60～100 nm、长度约30～60 μm。研究了AgNO₃溶液浓度、PVP和AgNO₃比例和控制剂浓度等对所得银纳米线形貌的影响。研究发现可以通过反应条件的改变来调节所得银纳米线的形貌。本方法的可能机理是由于引入的金属阳离子可以除掉吸附在晶种表面的氧,从而促进银纳米线的生长。     

Physico-Chemical Effects on the Scale-Up of Ag Photodeposition on TiO2 Nanoparticles

We have previously demonstrated that TiO₂ nanoparticles can be functionalized by photodeposition with silver or gold particles in the 1?C2 nm range presumed to be desirable for catalysis applications. However, the preparation of these samples directly on microscope grids, while conducive to particle size determinations, did not produce sufficient materials for reaction studies. We report here scale-up techniques designed to produce greater quantities of material for testing, while maintaining characteristics that contribute to uniformity in the deposition process. For the scale-up process, an irradiation source with highly uniform intensity is necessary to generate Ag/TiO₂ samples with consistent Ag loading. In addition, control of the precursor concentration is also required to produce Ag/TiO₂ samples with high Ag loading and narrow Ag size distribution. The optimum conditions for the scale-up process found in this study involved Ag photodeposition from a 5 × 10^?3 M AgNO₃ solution using a high pressure Hg lamp at 366 nm for 60 s. Under these reaction conditions, the size of Ag particles determined by TEM and HAADF-STEM imaging was within 1?C2 nm and the Ag loading was ~3.2 wt%. Achievement of this level of uniformity required control of the uniformity of illumination, as well as of the solution concentration and irradiation conditions. Higher solution concentrations and higher power led to the growth of larger (ca. 10 nm) silver particles. In contrast, the loading and size distribution of the Ag particles photodeposited were remarkably insensitive to the source and morphology of the TiO₂ nanoparticles utilized. No Ag peak was resolved in the XRD patterns for Ag/TiO₂ samples obtained from the optimized scale-up process, corroborating the size range determination of the Ag nanoparticles. XPS showed that the Ag particles in all cases were metallic Ag.     

Synthesis and characterization of polyaniline derivative and silver nanoparticle composites

BACKGROUND: There has been a recent surge of interest in the synthesis and applications of electroactive polymers with incorporated metal nanoparticles. These hybrid systems are expected to display synergistic properties between the conjugated polymers and the metal nanoparticles, making them potential candidates for applications in sensors and electronic devices. RESULTS: Composites of polyaniline derivatives—polyaniline, poly(2,5‐dimethoxyaniline) and poly(aniline‐2,5‐dimethoxyaniline)—and silver nanoparticles were prepared through simultaneous polymerization of aniline derivative and reduction of AgNO₃ in the presence of poly(styrene sulfonic acid) (PSS). We used AgNO₃ as one of the initial components (1) to form the silver nanoparticles and (2) as an oxidizing agent for initiation of the polymerization reaction. UV‐visible spectra of the synthesized nanocomposites reveal the synchronized formation of silver nanoparticles and polymer matrix. The morphology of the silver nanoparticles and degree of their dispersion in the nanocomposites were characterized by transmission electron microscopy. Thermogravimetric analysis and differential scanning calorimetry results indicate an enhancement of the thermal stability of the nanocomposites compared to the pure polymers. The electrical conductivity of the nanocomposites is in the range 10^?4 to 10^?2 S cm^?1. CONCLUSION: A single‐step process for the synthesis of silver nanoparticle–polyaniline derivative nanocomposites doped with PSS has been demonstrated. The approach in which silver nanoparticles are formed simultaneously during the polymerization process results in a good dispersion of the nanoparticles in the conductive polymer matrix. Copyright © 2008 Society of Chemical Industry     

A simple and effective route for the synthesis of nano-silver colloidal dispersions

In this work we develop a simple method to synthesize nanosized Ag colloids with the addition of urea which produce intermediates AgOCN and Ag₂CO₃ before the formation of silver. These intermediates are beneficial to obtaining high conversions of narrow size distributions of silver colloids from this synthesis process. At the molar ratio of [Urea]/[Ag⁺] = 4, [NaOH]/[Ag⁺] = 0.8, the weight ratio of PVP/AgNO₃ = 1 g/g, using dextrose as a reducing agent and a reaction temperature of 70 °C, we obtain silver colloids of average size 22 nm with a standard deviation of 4.7 nm after separation and washing procedures. The conversion under these conditions was nearly complete at about 98%. After a thorough washing procedure, the purity of silver colloids is up to 94.4% and its dried film is electrically conductive at room temperature. The electrical resistivity reached 4.5 × 10⁻⁶ Ω cm after 250 °C heating for 30 min.     

Sonochemical deposition of silver nanoparticles on linear low density polyethylene/cyclo olefin copolymer blend films

Silver nanoparticles were deposited on the surface of an extruded film of linear low density polyethylene/cyclo olefin copolymer (LLDPE/COC) blend by an ultrasound-assisted method. A series of LLDPE/COC/silver nanocomposites, containing 0.02, 0.05, 0.08 and 0.1 mol/L of AgNO₃ were prepared and characterized. The effect of ultrasound method on the silver deposition on the film surface was characterized as well as the effect of silver nanoparticles on their fungicidal characteristics. The silver action and biocide effect of the films were enhanced significantly as the silver content increased from 0.02 to 0.08 mol/L of AgNO₃ and after that no significant enhancement was observed. From the UV–Vis analysis and transmission electron microscopic observations, the particle shape, size and size distribution were determined. Films of LLDPE/COC blends with silver deposition exhibited a noticeable increase in water vapor barrier properties with the increase in the concentration of AgNO₃ and demonstrated good fungicidal activity, specifically against fungus Aspergillius niger. The observed results could be applied in the design of industrial films for packaging.     

Antibacterial Ag containing core-shell polyvinyl alcohol-poly (lactic acid) nanofibers for biomedical applications

Core-shell-structured polyvinyl alcohol (PVA)-poly (lactic acid) (PLA) nanofibers combining the hydrophilic trait of PVA and the biocompatibility of PLA were produced using coaxial electrospinning. This allowed the incorporation of AgNO₃ in the PVA core of the distinct fibers as shown through transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR). Scanning electron microscopy (SEM) showed relatively uniform and bead-free fibers with smooth surfaces. Ag-containing fibers show significantly decreased diameters compared with Ag-free samples as a result of the increased conductivity of the spinning solutions with increasing amounts of AgNO₃. In a postsynthetic treatment, the AgNO₃ was reduced forming silver nanoparticles (Ag NPs). Ag NPs of 45 to 90 nm size were located in the PVA core but also on the surface of the core-shell fibers and as individual, agglomerated, and polymer-coated particles of 100-200 nm. Powder X-ray diffraction (PXRD), energy dispersive X-ray spectroscopy (EDX), and UV-vis absorption spectroscopy confirmed the increasing amounts of Ag in the core-shell fibers when using increasing amounts of AgNO₃ in the spinning solutions. The antibacterial activity of the nanofiber mats against two prokaryotes Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) increased with increasing amounts of Ag, as expected and produces inhibition zones of 1 to 2 mm.     

Synthesis and intercalation of silver nanoparticles in kaolinite/DMSO complexes

Ag nanoparticles were synthesized in the interlamellar space of a layered kaolinite. Disaggregation of the lamellae of the nonswelling kaolinite was achieved by the intercalation of dimethyl sulfoxide (DMSO). The kaolinite was suspended in aqueous AgNO₃ solution and the adsorbed Ag⁺ ions were reduced on the surface of kaolinite lamellae with NaBH₄ or UV light irradiation. The silver nanoparticles formed were characterized by X-ray diffraction (XRD), small angle X-ray scattering (SAXS), and transmission electron microscopy (TEM). We studied the effects of the two reduction methods on the size and the size distribution of Ag nanoparticles and how clay mineral structure is altered as a consequence of particle formation. It was established that the size of Ag nanoparticles depends on both silver content and the reduction method. Photoreduction of silver led to the formation of relatively large Ag nanoparticles (diameter 8–14 nm).     

The formation and catalytic activity of silver nanoparticles in aqueous polyacrylate solutions

Silver nanoparticles (AgNPs) have been synthesized in the presence of polyacrylate through the reduction of silver nitrate by sodium borohydride in aqueous solution. The AgNO3 and polyacrylate carboxylate group concentrations were kept constant at 2.0 × 10^–4 and 1.0 × 10^–2 mol·L^–1, respectively, while the ratio of [NaBH₄]/[AgNO₃] was varied from 1 to 100. The ultraviolet-visible plasmon resonance spectra of these solutions were found to vary with time prior to stabilizing after 27 d, consistent with changes of AgNP size and distribution within the polyacrylate ensemble occurring. These observations, together with transmission electron microscopic results, show this rearrangement to be greatest among the samples at the lower ratios of [NaBH₄]/[AgNO₃] used in the preparation, whereas those at the higher ratios showed a more even distribution of smaller AgNP. All ten of the AgNP samples, upon a one thousand-fold dilution, catalyze the reduction of 4-nitrophenol to 4-aminophenol in the temperature range 283.2–303.2 K with a substantial induction time being observed at the lower temperatures.

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Synthesis and characterization of novel silver/L‐phenylalanine‐based optically active polyacrylate nanocomposite

Novel bioactive and optically active poly(N‐acryloyl‐L ‐phenylalanine) (PAPA) was synthesized by atom transfer radical polymerization. PAPA‐silver (Ag) nanocomposites have been successfully prepared via in situ reducing Ag⁺ ions anchored in the polymer chain using hydrazine hydrate as reducing agent in an aqueous medium. By controlling of the amount of Ag⁺ ions introduced, we have produced an organic/inorganic nanocomposite containing Ag nanoparticles with well controlled size. Nanocomposites were characterized by X‐ray diffraction (XRD), UV–Vis spectrophotometry, transmission electron microscopy, and Fourier transform infrared. XRD pattern showed presence of Ag nanoparticles. The PAPA/Ag nanocomposites with 1 : 10 silver nitrate (AgNO₃) : PAPA ratio revealed the presence of well‐dispersed Ag nanoparticles in the polymer matrix. All of these Ag nanoparticles formed are spherical and more than 80% of them are in the range of 15–25 nm. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Fabrication and characterization of chitosan/poly(vinyl alcohol) electrospun nanofibrous membranes containing silver nanoparticles for antibacterial water filtration

Electrospun nanofibrous membranes (ENMs) were fabricated based on chitosan/poly(vinyl alcohol) (CS/PVA) with a 70/30 mass ratio containing silver nanoparticles (AgNPs) via the electrospinning method. AgNPs were produced on the surface of CS/PVA nanofibers by adding AgNO₃ to a CS/PVA blend solution as a silver rendering component. The presence of AgNPs in the polymer blend solution was detected by UV spectrophotometry. The morphology of nanofibers before and after cross-linking with glutaraldehyde was investigated by the field emission scanning electron microscopy. The formation and size distribution of AgNPs onto the surface of nanofibers were observed by transmission electron microscopy and confirmed by energy dispersing X-ray spectroscopy. As-spun and cross-linked CS/PVA nanofibers revealed a smooth surface with diameters ranging from 58 to 73 nm and 95 to 109 nm, respectively. The effect of AgNP formation on the chemical structure of nanofibers was explored by Fourier transform infrared spectroscopy. Static and dynamic antibacterial filtration efficiencies of CS/PVA ENMs, containing differing amounts of AgNO₃, have been tested against Escherichia coli, a gram negative bacterium. The antibacterial assessment results exhibited a significant increase in both static and dynamic antibacterial filtration efficiencies of the prepared CS/PVA ENMs by addition of AgNO₃ as a bactericidal agent.