Effective chemical route for the synthesis of silver nanostructures in formamide

Poly(N-vinyl-2-pyrrolidone) (PVP) and gelatin protected silver nanostructures are prepared in formamide by simple chemical route. Both PVP and gelatin stabilized silver nanoparticles in formamide lead to the formation of nanostructures of various definite geometric shapes and sizes. The effect of anisotropy on the surface plasmon absorption band is analyzed by monitoring the UV-Visible absorption spectra of gelatin stabilized silver nanoparticles. The particles were characterized by UV-Visible absorption spectra and TEM.     

Synthesis of hollow bimetal particles based on silver and gold

A pioneering procedure is presented for the photochemical synthesis of aqueous solutions of hollow bimetal silver-gold nanoparticles in the presence of poly-N-vinylpyrrolidone. The structure and properties of synthesized nanocages were studied by the methods of high-resolution transmission electron microscopy, UV visible spectroscopy, and energy-dispersive X-ray structural analysis. The mechanism of the formation of AgAu nanocages was suggested on the basis of the experimental data.     

Extraction and preconcentration of anthocyan dye from aqueous solutions with water-soluble poly-N-vinylamides

Extraction of an anthocyan dye with poly-N-vinylpyrrolidone (PVP) and poly-N-vinylcaprolactam (PVC) under the conditions of separation of aqueous solutions of this polymer into two phases in the presence of salting-out agents (sodium chloride and sodium or ammonium sulfate) was studied.     

Sodium silicate route to coat polymer particles with silica

This paper presents a low-cost method to coat polymer particles with silica nanoparticles from inexpensive sodium silicate solution, which is a less-common precursor compared with tetraethyl orthosilicate for coating of polymer particles. The method is based on deposition of active silicic acid in the presence of polymer particles, prepared by emulsion polymerization of styrene involving poly(N-vinyl-2-pyrrolidone), under conditions that a dilute silica sol can be formed from this active silicic acid. The whole process was conducted in aqueous media. The effects of different reaction parameters, such as reaction temperature, amount of active silicic acid and solution pH, on the morphology and size of composite particles were investigated.     

Characterization of CdS nanoparticles in solutions of P(TFE-co-PVDF-co-Prop)/N,N-dimethylformamide

We report in here the preparation of CdS nanoparticles (Q-CdS) in N,N-dimethylformamide (DMF) and poly(tetrafluoroethylene-co-vinylidenefluoride-co-propylene) (PTFE-co-PVDF-co-Prop) by reaction of cadmium acetate and thiourea at room temperature. The formation and size evolution of Q-CdS particles were followed by optical absorption spectroscopy as a function of the aging process of the solutions. The obtained results indicated that not only the Q-CdS particles were more stable in DMF than in aqueous solutions, probably due to the interaction with the CHNO group, but also they were formed in smaller sizes. The particle size obtained in DMF was estimated in 4-6 nm against 10-20 nm in aqueous solution. The results also showed that the velocity of Q-CdS formation is lower when the reaction was carried out in PTFE-co-PVDF-co-Prop dissolved in DMF. The Q-CdS particles formed in this system were also less stable than in pure DMF, probably due to the interaction of the CHNO fragment and CF₂ of polymer chain or phase segregation.     

Lyotropic liquid crystal-assisted synthesis of micro- and nanoparticles of silver

A simple, one-step approach for the synthesis of micro- and nanoparticles of silver by employing a lyotropic liquid crystal (LLC) template is described. Anisotropic silver particles are synthesised by reducing an appropriate amount of precursor silver nitrate using a mild reducing agent ascorbic acid in presence of a hexagonal LLC medium, without the aid of any external stabilising agents. In this synthesis, precursor concentration, type of the reducing agent and LLC phase are found to significantly influence the particle size and morphology. Either a decrease in the concentration of silver nitrate or a change in the reducing agent, from ascorbic acid to sodium borohydride in the same reaction medium, yielded quasi-spherical nanoparticles. Besides, replacing the hexagonal LLC medium with a lamellar phase during the synthesis using ascorbic acid also resulted in the formation of spherical particles in nanometre scale. As a comparison, gold nanoparticle synthesis is carried out in hexagonal and lamellar LLC phases. Similar to the observations made in the silver particle synthesis, branched anisotropic particles are formed in the hexagonal phase and quasi-spherical particles are produced in the lamellar phase. A possible growth mechanism for the formation of these particles based on the phase structure of the LLC medium is discussed.     

Synthesis and biological activity of new polymeric silver-containing nanocomposites

Russian Chemical Bulletin - The formation of new polymeric nanocomposites with silver nanoparticles incorporated into the matrix of 1-vinyl-1,2,4-triazole copolymers with vinyl acetate was studied....     

Competition between polyelectrolyte macromolecules and amphiphilic polymer micelles in interaction with copper nanoparticles

Competition between poly(1,2-dimethyl-5-vinylpyridinium methyl sulfate) polycationic macromolecules and micelles of amphiphilic polymers containing hydrophilic and hydrophobic blocks (polyethylene glycol-600 monolaurate and poly-N-vinylpyrrolidone monostearate) for copper nanoparticles was studied by means of electrophoresis and electron microscopy techniques. It was shown that, irrespective of the formation method, almost all copper nanoparticles were bonded to the polycation in polycation-polyethylene glycol-600 monolaurate mixed solutions but were distributed between the polymers in polycation-poly-N-vinylpyrrolidone monostearate mixtures. It was concluded that the stability of the complex of copper nanoparticles with the polycation is higher than that with polyethylene glycol-600 monolaurate and is comparable with that of the copper particle-poly-N-vinylpyrrolidone monostearate complex.     

Interaction of copper nanoparticles with liposomes

The reduction of copper(II) ions in an aqueous dispersion of positively charged liposomes results in the formation of stable sols of a complex of copper nanoparticles with the surface of liposomes. The mean size (7 nm) and the narrow size distribution of metal nanoparticles are similar to those observed in the case of metal sol formation in polymer solutions. The labile character of bonds between nanoparticles and liposomes makes the latter able to compete with a linear polymer (poly-N-vinylpyrrolidone) in binding to nanoparticles. This ability is manifested in the independence of an almost even distribution of nanoparticles between these competitors from the sol preparation mode in a system including both poly(N-vinylpyrrolidone) macromolecules and liposomes. The evenness of the distribution indicates an approximately identical stability of complexes of copper nanoparticles with both competitors. The replacement of liposomes with poly(N-vinylpyrrolidone) macromolecules in the protective shields of nanoparticles is accompanied by the detachment of the nanoparticles from the surface, thereby allowing the measurement of their size and size distribution in the case where such measurements are impossible because of a high density of nanoparticles on the liposome surface.     

Nanosize metal clusters in polymer systems

Three synthetic methods have been developed for embedding nanosize metal clusters into polymers: (i) in situ synthesis of silver nanoparticles in cross-linked poly-acrylamide gels, (ii) implantation of cryochemically produced silver nanoparticles into poly-acrylamide gels, and (iii) encapsulation of metal nanoparticles in poly-p-xylylene films. All methods allow one to produce 3–20 nm stable metal clusters embedded into bulk materials, thin films or fine particles dispersed in organic solvents or water. Results on some physical properties of the metal-polymer systems thus obtained are presented.     

Structure of nanocomposites based on lead sulfide and poly-<Emphasis Type="Italic">p</Emphasis>-xylylene

Nanocomposites containing controlled (in the course of synthesis) concentrations of lead sulfide nanoparticles dispersed in the polymer matrix were prepared by the method of gas-phase polymerization on the surface of an active monomer, paracyclophane, which was codeposited with lead sulfide molecules. According to wide-angle X-ray diffraction measurements, the prepared nanocomposites contain lead sulfide clusters of 4 nm size, which are localized in the amorphous regions of poly-p-xylylene. Size distribution curves for lead sulfide particles as calculated on the basis of the Fourier analysis of crystallographic X-ray reflections and the volume distributions functions of particles as determined from small-angle X-ray scattering data are reported. A mechanism for the formation of lead sulfide nanoparticles in the poly-p-xylylene matrix is proposed on the basis of analysis of the X-ray scattering curves.     

Gold-copolymer nanoparticles: Poly(ε-caprolactone)/poly(N-vinyl-2-pyrrolydone) Biodegradable triblock copolymer as stabilizer and reductant

Block copolymers have been extensively used in the synthesis of many types of nanoparticles, where generally are considered as stabilizer and protective agent. In this work a double function of the biodegradable triblock copolymer poly(N-vinyl-2-pyrrolidone)-b-poly(ε-caprolactone)-b-poly(N-vinyl-2-pyrrolidone), (PVP-PCL-PVP) in the gold nanoparticle-copolymer synthesis is reported.Gold-copolymer composed nanoparticles were synthesized using the triblock copolymer (PVP-PCL-PVP) and potassium tetrachloro aurate (III), both in aqueous solution. The copolymer work as both, reductant and stabilizer agent. The obtained nanoparticles were characterized by FT-IR, dynamic light scattering (DLS), atomic force microscopy (AFM) and transmission electron microscopy (TEM). The shape and the size of the obtained nanoparticles are dependent on the copolymer/salt of gold concentration ratio used in the synthesis.To complement the experimental results about the copolymer role in the nanoparticles synthesis, computational tools were used to characterize the reactivity of the reactant species.     

Fe-containing nanocomposites based on a biocompatible copolymer 1-vinyl-1,2,4-triazole with <Emphasis Type="Italic">N</Emphasis>-vinylpyrrolidone

New polymer nanocomposites containing iron oxide nanoparticles stabilized with a biocompatible copolymer of 1-vinyl-1,2,4-triazole with N-vinylpyrrolidone were produced. The synthesis was conducted using the method of chemical reduction of iron ions with hydrazine hydrate in an aqueous medium in the presence of a polymer matrix. The ESR spectroscopy data showed that the core—shell type nanoparticles were obtained. The core generally consistsed of zero-valence iron coated with an oxide shell. According to the data of transmission electron microscopy, the obtained polymer nanocomposites consisted of nanoparticles of mainly spherical shape with a diameter from 1 to 14 nm. Aggregates formed from individual stabilized nanoparticles of up to 75 nm in size (in most cases) were also observed. These aggregated particles were found to self-organize and form branched chains. Nanocomposites were characterized by a different particle-size distribution, which was determined by the initial ratio of the copolymer and the precursor of iron nanoparticles.     

Photochemical synthesis of Ag/Cu bimetal particles with a nucleus-shell structure

An effective procedure for the synthesis of bimetal nanoparticles Ag nucleus-Cu shell was developed. The use of a composition based on Na₂[CuEDTA] and AgNO₃ with N-polyvinylpyrrolidone as a stabilizer of nanoparticles is optimal for the synthesis of bimetal particles. Spectral characteristics of the bimetal nanoparticles were investigated, and the kinetics of the metal phase formation in aqueous solutions was studied.     

琥珀酸二异辛酯磺酸钠微乳体系中纳米银的制备及其连续相的影响

在琥珀酸二异辛酯磺酸钠(AOT)为表面活性剂、环己烷为连续相形成的微乳体系中, 利用水合肼还原AgNO₃制备了分散性良好的纳米银. 利用紫外-可见(UV-Vis)光谱和透射电镜(TEM)对所得产物进行了表征, TEM显微图像表明形成粒子为球形结构, 平均粒径为5.10 nm, 标准偏差为2.84 nm. 分别利用正己烷、正庚烷、正辛烷、环己烷和十二烷等作连续介质, 研究了微乳液中连续相对纳米银形成的影响. 随着正烷烃碳链长度的增加, 微乳液中胶束之间的交换速率增大, 形成粒子的平均粒径逐渐减小. 十二烷形成的微乳体系制备的纳米银溶胶具有最宽的共振吸收峰, 所得的纳米银粒子平均粒径最小. 环己烷形成的微乳液中反胶束具有特殊的界面强度, 导致纳米银晶核的形成速率过低, 纳米银晶粒的生长不完全.     

Formation of long-lived clusters and silver nucleation in the γ-irradiation of aqueous silver perchlorate solutions containing polyphosphate

It was found that long-lived positively charged and neutral silver clusters were formed by the radiation-chemical reduction of Ag⁺ ions in aqueous solutions containing sodium polyphosphate. The nuclearity of the clusters increased with absorbed dose; then, quasi-metal particles were formed. The process culminated in the formation of silver nanoparticles.Translated from Khimiya Vysokikh Energii, Vol. 39, No. 2, 2005, pp. 83–87.Original Russian Text Copyright © 2005 by Ershov, Abkhalimov, Sukhov.This revised version was published online in April 2005 with a corrected cover date.     

Formation of copper sols via reduction of Cu2+ ions in solutions of cationic and anionic polyelectrolytes

Zero-valence copper sols are prepared at 20°C via the chemical reduction of Cu(II) ions in aqueous solutions of high-molecular-mass cationic and anionic polyelectrolytes [(poly(1,2-dimethyl-5-vinylpyridium methyl sulfate) and poly(sodium styrenesulfonate), respectively]. In both sols, metal nanoparticles are characterized by narrow size distribution, indicating the pseudomatrix mechanism of their formation; however, the diameter of spherical copper particles formed in the polycation solution (3–14 nm) is much smaller than that of particles formed in the solution of polyanion (10–30 nm). Causes of different sizes of metal nano-particles formed in solutions of polyelectrolytes with different chain charges are discussed in terms of the pseudomatrix mechanism of new phase synthesis in polymer solutions and classical electrocapillary theory.     

Synthesis of Silver and Gold Nanoparticles by a Novel Electrochemical Method

Spherical silver and gold nanoparticles with narrow size distributions were conveniently synthesized in aqueous solution by a novel electrochemical method. The technological keys to the electrochemical synthesis of monodispersed metallic nanoparticles lie in the choice of an ideal stabilizer for the metallic nanoclusters and the use of a rotating platinum cathode. Poly(N‐vinylpyrrolidone) (PVP) was chosen as the stabilizer for the silver and gold clusters. PVP not only protects metallic particles from agglomeration, but also promotes metal nucleation, which tends to produce small metal particles. Using a rotating platinum cathode effectively solves the technological difficulty of rapidly transferring the (electrochemically synthesized) metallic nanoparticles from the cathode vicinity to the bulk solution, avoiding the occurrence of flocculates in the vicinity of the cathode, and ensuring the monodispersity of the particles. The particle size and particle size distribution of the silver and gold nanoparticles were improved by adding sodium dodecyl benzene sulfonate (SDBS) to the electrolyte. The electrochemically synthesized nanoparticles were characterized by TEM and UV/Vis spectroscopy.     

Synthesis and optical properties of poly(N-isopropylacrylamide) nanogel containing silver nanoparticles

Composite nanoparticles representing silver nanoparticle-containing polymer gels have been synthesized. The synthesis comprises two main stages. Initially, monodisperse hydrogel particles with a controlled diameter of approximately 500 nm are obtained by N-isopropylacrylamide polymerization. Then, silver ions are reduced on the surface of the polymer network. Variations in the concentration ratio between reductants and silver nitrate make it possible to produce silver nanoparticles with sizes in a range of 10–30 nm and different packing densities on the gel particle surface. The resultant nanocomposites have been studied by transmission electron microscopy, spectrophotometry, and dynamic light scattering. Depending on the size and packing density of the silver nanoparticles on the polymer particle surface, the plasmon resonance of the nanocomposites varies in a range of 420–750 nm, which determines variations in the color of the colloid from yellow, orange, and red to blue and blue-green. After the inclusion of silver nanoparticles, nanogels of poly(N-isopropylacrylamide) retain their capability for thermosensitive phase transition with a lower critical mixing temperature of 31°C.     

Photochemical Synthesis of Anisotropic Silver Nanoparticles in Aqueous Solutions in the Presence of Sodium Citrate

The rapid one-step photochemical synthesis of anisotropic silver nanoparticles (ANPs) is reported. Silver ANPs were prepared from silver nitrate by a citrate route in aqueous solutions at room temperature under exposure to unfiltered light of a DRK 120 high-pressure mercury lamp. The silver ANPs form through one-electron reduction of the silver cation in its chelate complex with the production of sodium citrate photolysis. In the course of synthesis, small charged silver clusters and nanoparticles are formed first, which are then stabilized by citrate ions. Key factors that influence the synthesis of silver ANPs and their further transformation have been determined.