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Sample records for based nanoparticles synthesis

  1. Green Chemistry Based Benign Routes for Nanoparticle Synthesis

    Directory of Open Access Journals (Sweden)

    Parth Malik

    2014-01-01

    Full Text Available Green chemistry has been an eye catching area of interest since the past few years. With the problem of energy crisis looming high and its constraint being particularly vulnerable on the developing economies, the need for giving alternative traditional chemistry a serious consideration as well as adequate room for development has received significant boost through the coveted efforts of multidisciplinary and interdisciplinary scientific fields. Nanoscience has been the right field in this dimension as it opens up the door to multiple opportunities through enabling a number of chemical, biochemical, and biophysical transformations in a significantly easier and reliable manner. The use of nanoparticles has made the fields of catalysis, synthesis, and enzyme immobilizations as well as molecular interactions a lot much easier, rapid and easily controllable. This review article sheds light on the popular alternative synthesis routes being employed for the synthesis of nanoparticles, the pivotal being from microbes, plants, and chemical routes via sonication, microwaving, and many others.

  2. Microemulsion Synthesis of Nanoparticles

    Directory of Open Access Journals (Sweden)

    Gotić, M.

    2013-11-01

    Full Text Available Nanoparticles and nanomaterials have wide applications in electronics, physics, material design, being also utilized as sensors, catalysts, and more and more in biomedicine. Microemulsions are an exceptionally suitable medium for the synthesis of nanoparticles due to their thermodynamical stability, great solubility of both polar and nonpolar components, as well as their ability to control the size, dispersity and shape of the particles. This review presents microemulsion techniques for the synthesis of inorganic nanoparticles. It takes place in water-in-oil microemulsions by mixing one microemulsion with a cationic precursor, and the other with a precipitating or reducing agent, or by direct addition of reducing agents or gas (O2, NH3 ili CO2 into microemul sion (Fig. 1. Metal nanoparticles are used as catalysts, sensors, ferrofluids etc. They are produced by reducing the metal cation with a suitable reducing agent. In a similar way, one can prepare nanoparticles of alloys from the metal salts, provided that the metals are mutually soluble. The microemulsion technique is also suitable for depositing nanoparticles onto various surfaces. Highly active catalysts made from nanoparticles of Pt, Pd, Rh and other noble metals may be obtained in this way. Metal oxides and hydroxides may be prepared by hydrolysis or precipitation in the water core of microemulsion. Precipitation can be initiated by adding the base or precipitating agent into the microemulsion with water solution of metal ions. Similarly, nanoparticles may be prepared of sulphides, halogenides, cyanides, carbonates, sulphates and other insoluble metal salts. To prevent oxidation of nanoparticles, especially Fe, the particles are coated with inert metals, oxides, various polymers etc. Coating may provide additional functionality; e.g. coating with gold allows subsequent functionalization with organic compounds containing sulphur, due to the strong Au–S bond. Polymer coatings decrease

  3. Nanoparticles synthesis of tungsten disulfide via AOT-based microemulsions

    International Nuclear Information System (INIS)

    Graphical abstract: A controlled synthesis of WS2 nanoparticles (most probably inorganic fullerene (IF)) via microemulsion was applied for the first time to prepare WS2 (7–12 nm) by acidification of the water cores of the AOT reverse microemulsion. Highlights: ► An innovative reverse microemulsion technique was developed for WS2 synthesis. ► WS2 nanoparticles were obtained with narrow size distribution in range of 7–12 nm. ► Operating cost of microemulsion was lower in contrast to quartz reactor method. ► WS2 morphology could be controlled to obtain highly active and selective catalysts. ► Lower size of WS2 in this study overcomes the shortcoming of quartz reactor method. -- Abstract: The tungsten disulfide (WS2) nanoparticles (most probably inorganic fullerene (IF)) with a narrow size distribution were synthesized by a reverse micelle technique for the first time. The particle size was controlled by varying water-to-surfactant molar ratio (W0), aging time and reagent concentration. The synthesized WS2 nanoparticles were characterized by zetasizer, UV–visible spectrophotometers and transmission electron microscopy (TEM). The WS2 nanoparticles with particle diameter size of 7–12 nm were obtained via 24 h aging time. The particle size was controlled by changing the aging time and molar ratio of water/surfactant. Doubling W0 increased the amount and particle size of WS2 by 22 and 26%, respectively. The effect of aging time in the range of 6–24 h was investigated and the complete disappearance of yellowish color at 24 h resulted in an optically clear solution, which was the indication of WS2 formation with 100% conversion of reactant ((NH4)2WS4) in the batch reactor.

  4. Cobalt-based Magnetic Nanoparticles: Design, Synthesis and Characterization

    Science.gov (United States)

    Zamanpour, Mehdi

    The ever-increasing desire for more energy attainable from a smaller volume of matter has driven researchers to explore advanced materials at the molecular or even atomic size scale. Magnetic materials at the nanometer size scale have been the subject of enormous research effort worldwide for more than half a century. Different magnetic nanoparticles have shown different behavior in the absence and presence of an external magnetic field, which has led them to be categorized as soft (easy to demagnetize) or hard (resistive against demagnetization) magnets. Applications range from medical and biomedical devices to magnetic recording media and magnetic sensing have emphasized the importance of this class of materials. Soft magnetic phases have found application in power generation and magnetic targeted drug delivery, while hard magnets have been subject of extensive research for application as energy storage media. Discovery of the exchange-coupling phenomenon between the spins of two adjacent hard and soft magnetic phases which means taking advantage of both high magnetic moment of the soft phase as well as high coercivity of the hard phase has attracted scientists to develop advanced materials for energy storage with no usage of fossil fuels: clean energy. In this Dissertation, synthesis of pure phase, soft FeCo nanoparticles with high magnetic moment and hard phase CoxC nanoparticles possessing high coercivity is reported. The polyol method (chemical co-precipitating at polyhydric alcohol as reducing agent) is used to make FeCo and Co xC nanoparticles and the effects of important reaction kinetics parameters on the structure and magnetic properties of the products are studied. Careful analysis of correlations between these parameters and the properties of the magnetic particles has made synthesis of FeCo and CoxC nanoparticles with desired properties possible. Fabrication of MnAlC-FeCo heterostructures as a rare earth-free alternative for high-performance permanent

  5. Core shell hybrids based on noble metal nanoparticles and conjugated polymers: synthesis and characterization

    OpenAIRE

    Battocchio Chiara; Polzonetti Giovanni; Cametti Cesare; Fratoddi Ilaria; Venditti Iole; Russo Maria

    2011-01-01

    Abstract Noble metal nanoparticles of different sizes and shapes combined with conjugated functional polymers give rise to advanced core shell hybrids with interesting physical characteristics and potential applications in sensors or cancer therapy. In this paper, a versatile and facile synthesis of core shell systems based on noble metal nanoparticles (AuNPs, AgNPs, PtNPs), coated by copolymers belonging to the class of substituted polyacetylenes has been developed. The polymeric shells cont...

  6. Gas Phase Nanoparticle Synthesis

    Science.gov (United States)

    Granqvist, Claes; Kish, Laszlo; Marlow, William

    This book deals with gas-phase nanoparticle synthesis and is intended for researchers and research students in nanomaterials science and engineering, condensed matter physics and chemistry, and aerosol science. Gas-phase nanoparticle synthesis is instrumental to nanotechnology - a field in current focus that raises hopes for environmentally benign, resource-lean manufacturing. Nanoparticles can be produced by many physical, chemical, and even biological routes. Gas-phase synthesis is particularly interesting since one can achieve accurate manufacturing control and hence industrial viability.

  7. Infrared Radiation Assisted Stokes’ Law Based Synthesis and Optical Characterization of ZnS Nanoparticles

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    Beer Pal Singh

    2016-01-01

    Full Text Available The strategy and technique exploited in the synthesis of nanostructure materials have an explicit effect on the nucleation, growth, and properties of product materials. Nanoparticles of zinc sulfide (ZnS have been synthesized by new infrared radiation (IR assisted and Stokes’ law based controlled bottom-up approach without using any capping agent and stirring. IR has been used for heating the reaction surface designed in accordance with the well-known Stokes law for a free body falling in a quiescent fluid for the synthesis of ZnS nanoparticles. The desired concentration of aqueous solutions of zinc nitrate (Zn(NO32·4H2O and thioacetamide (CH3CSNH2 was reacted in a controlled manner by IR radiation heating at the reaction area (top layer of reactants solution of the solution which results in the formation of ZnS nanoparticles at ambient conditions following Stokes’ law for a free body falling in a quiescent fluid. The phase, crystal structure, and particle size of as-synthesized nanoparticles were studied by X-ray diffraction (XRD. The optical properties of as-synthesized ZnS nanoparticles were studied by means of optical absorption spectroscopic measurements. The optical energy band gap and the nature of transition have been studied using the well-known Tauc relation with the help of absorption spectra of as-synthesized ZnS nanoparticles.

  8. Synthesis and Bioconjugation of Gold Nanoparticles as Potential Molecular Probes for Light-Based Imaging Techniques

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    Raja Gopal Rayavarapu

    2007-01-01

    Full Text Available We have synthesized and characterized gold nanoparticles (spheres and rods with optical extinction bands within the “optical imaging window.” The intense plasmon resonant driven absorption and scattering peaks of these nanoparticles make them suitable as contrast agents for optical imaging techniques. Further, we have conjugated these gold nanoparticles to a mouse monoclonal antibody specific to HER2 overexpressing SKBR3 breast carcinoma cells. The bioconjugation protocol uses noncovalent modes of binding based on a combination of electrostatic and hydrophobic interactions of the antibody and the gold surface. We discuss various aspects of the synthesis and bioconjugation protocols and the characterization results of the functionalized nanoparticles. Some proposed applications of these potential molecular probes in the field of biomedical imaging are also discussed.

  9. Synthesis and characterisation of highly fluorescent core-shell nanoparticles based on Alexa dyes

    Energy Technology Data Exchange (ETDEWEB)

    Natte, Kishore; Behnke, Thomas; Orts-Gil, Guillermo, E-mail: guillermo.orts-gil@bam.de; Wuerth, Christian; Friedrich, Joerg F.; Oesterle, Werner; Resch-Genger, Ute, E-mail: ute.resch@bam.de [BAM Federal Institute for Materials Research and Testing (Germany)

    2012-02-15

    Current and future developments in the emerging field of nanobiotechnology are closely linked to the rational design of novel fluorescent nanomaterials, e.g. for biosensing and imaging applications. Here, the synthesis of bright near infrared (NIR)-emissive nanoparticles based on the grafting of silica nanoparticles (SNPs) with 3-aminopropyl triethoxysilane (APTES) followed by covalent attachment of Alexa dyes and their subsequent shielding by an additional silica shell are presented. These nanoparticles were investigated by dynamic light scattering (DLS), transmission electron microscopy (TEM) and fluorescence spectroscopy. TEM studies revealed the monodispersity of the initially prepared and fluorophore-labelled silica particles and the subsequent formation of raspberry-like structures after addition of a silica precursor. Measurements of absolute fluorescence quantum yields of these scattering particle suspensions with an integrating sphere setup demonstrated the influence of dye labelling density-dependent fluorophore aggregation on the signaling behaviour of such nanoparticles.

  10. Surfactant Effects on Microemulsion-Based Nanoparticle Synthesis

    Directory of Open Access Journals (Sweden)

    Concha Tojo

    2010-12-01

    Full Text Available The effect of the surfactant on the size, polydispersity, type of size distribution and structure of nanoparticles synthesized in microemulsions has been studied by computer simulation. The model simulates the surfactant by means of two parameters: the intermicellar exchange parameter, kex, related to dimer life time, and film flexibility parameter, f, related to interdroplet channel size. One can conclude that an increase in surfactant flexibility leads to bigger and polydisperse nanoparticle sizes. In addition, at high concentrations, the same reaction gives rise to a unimodal distribution using a flexible surfactant, and a bimodal distribution using a rigid one. In relation to bimetallic nanoparticles, if the nanoparticle is composed of two metals with a moderate difference in reduction potentials, increasing the surfactant flexibility modifies the nanoparticle structure, giving rise to a transition from a nanoalloy (using a rigid film to a core-shell structure (using a flexible one.

  11. Pseudo-template synthesis of gold nanoparticles based on polyhydrosilanes

    Energy Technology Data Exchange (ETDEWEB)

    Sacarescu, Liviu, E-mail: livius@icmpp.ro [Petru Poni Institute of Macromolecular Chemistry, Aleea Grigore Ghica Voda 41A, Iasi 700487 (Romania); Simionescu, Mihaela; Sacarescu, Gabriela [Petru Poni Institute of Macromolecular Chemistry, Aleea Grigore Ghica Voda 41A, Iasi 700487 (Romania)

    2011-02-01

    Highly stable colloidal gold nanoparticles are obtained in a pseudo-template system using a specific polyhydrosilane copolymeric structure. This process takes place in situ by microwaves activation of the polymer solution in a non-polar solvent followed by stirring with solid HAuCl{sub 4} in natural light. The experimental procedure is very simple and the resulted colloidal gold solution is indefinitely stable. The specific surface plasmon resonance absorption band of the gold nanoparticles is strongly red shifted and is strictly related to their size. AFM correlated with DLS analysis showed flattened round shaped colloidal polymer-gold nanoparticles with large diameters. SEM-EDX combined analysis reveals that the polysilane-gold nanoparticles show a natural tendency to auto-assemble in close packed structures which form large areas over the polymer film surface.

  12. Tracking of the organic species during the synthesis of cobalt-based nanoparticles in non-aqueous solution

    Science.gov (United States)

    Staniuk, M.; Niederberger, M.; Koziej, D.

    2014-08-01

    In this work we investigate the organic products of the synthesis of Co-based nanoparticles in benzyl alcohol. Our GC and in situ IR studies provide the experimental proofs for the formation of benzaldehyde, toluene and isopropanol in the reaction solution. These organic products can be correlated with formation of cobalt-based nanoparticles with oxidation state from 0 to 3+. These results shine the light on the complexity of organic and inorganic reactions in solution during crystallization of nanoparticles.

  13. Luminescent Rare-earth-based Nanoparticles: A Summarized Overview of their Synthesis, Functionalization, and Applications.

    Science.gov (United States)

    Escudero, Alberto; Carrillo-Carrión, Carolina; Zyuzin, Mikhail V; Parak, Wolfgang J

    2016-08-01

    Rare-earth-based nanoparticles are currently attracting wide research interest in material science, physics, chemistry, medicine, and biology due to their optical properties, their stability, and novel applications. We present in this review a summarized overview of the general and recent developments in their synthesis and functionalization. Their luminescent properties are also discussed, including the latest advances in the enhancement of their emission luminescence. Some of their more relevant and novel biomedical, analytical, and optoelectronic applications are also commented on. PMID:27573400

  14. Gold Nanoparticle Microwave Synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Krantz, Kelsie E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Christian, Jonathan H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Coopersmith, Kaitlin [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Washington, II, Aaron L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Murph, Simona H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-07-27

    At the nanometer scale, numerous compounds display different properties than those found in bulk material that can prove useful in areas such as medicinal chemistry. Gold nanoparticles, for example, display promise in newly developed hyperthermia therapies for cancer treatment. Currently, gold nanoparticle synthesis is performed via the hot injection technique which has large variability in final particle size and a longer reaction time. One underdeveloped area by which these particles could be produced is through microwave synthesis. To initiate heating, microwaves agitate polar molecules creating a vibration that gives off the heat energy needed. Previous studies have used microwaves for gold nanoparticle synthesis; however polar solvents were used that partially absorbed incident microwaves, leading to partial thermal heating of the sample rather than taking full advantage of the microwave to solely heat the gold nanoparticle precursors in a non-polar solution. Through this project, microwaves were utilized as the sole heat source, and non-polar solvents were used to explore the effects of microwave heating only as pertains to the precursor material. Our findings show that the use of non-polar solvents allows for more rapid heating as compared to polar solvents, a reduction in reaction time from 10 minutes to 1 minute, maximizes the efficiency of the reaction, and allows for reproducibility in the size/shape of the fabricated nanoparticles.

  15. Gold Nanoparticle Microwave Synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Krantz, Kelsie E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Christian, Jonathan H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Coopersmith, Kaitlin [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Washington, II, Aaron L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Murph, Simona H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-07-27

    At the nanometer scale, numerous compounds display different properties than those found in bulk material that can prove useful in areas such as medicinal chemistry. Gold nanoparticles, for example, display promise in newly developed hyperthermia therapies for cancer treatment. Currently, gold nanoparticle synthesis is performed via the hot injection technique which has large variability in final particle size and a longer reaction time. One underdeveloped area by which these particles could be produced is through microwave synthesis. To initiate heating, microwaves agitate polar molecules creating a vibration that gives off the heat energy needed. Previous studies have used microwaves for gold nanoparticle synthesis; however, polar solvents were used that partially absorbed incident microwaves, leading to partial thermal heating of the sample rather than taking full advantage of the microwave to solely heat the gold nanoparticle precursors in a non-polar solution. Through this project, microwaves were utilized as the sole heat source, and non-polar solvents were used to explore the effects of microwave heating only as pertains to the precursor material. Our findings show that the use of non-polar solvents allows for more rapid heating as compared to polar solvents, and a reduction in reaction time from 10 minutes to 1 minute; this maximizes the efficiency of the reaction, and allows for reproducibility in the size/shape of the fabricated nanoparticles.

  16. Lactobacillusassisted synthesis of titanium nanoparticles

    Directory of Open Access Journals (Sweden)

    Jha Anal

    2007-01-01

    Full Text Available AbstractAn eco-friendlylactobacillussp. (microbe assisted synthesis of titanium nanoparticles is reported. The synthesis is performed at room temperature. X-ray and transmission electron microscopy analyses are performed to ascertain the formation of Ti nanoparticles. Individual nanoparticles as well as a number of aggregates almost spherical in shape having a size of 40–60 nm are found.

  17. Photo-synthesis of protein-based nanoparticles and the application in drug delivery

    International Nuclear Information System (INIS)

    Recently, protein-based nanoparticles as drug delivery systems have attracted great interests due to the excellent behavior of high biocompatibility and biodegradability, and low toxicity. However, the synthesis techniques are generally costly, chemical reagents introduced, and especially present difficulties in producing homogeneous monodispersed nanoparticles. Here, we introduce a novel physical method to synthesize protein nanoparticles which can be accomplished under physiological condition only through ultraviolet (UV) illumination. By accurately adjusting the intensity and illumination time of UV light, disulfide bonds in proteins can be selectively reduced and the subsequent self-assembly process can be well controlled. Importantly, the co-assembly can also be dominated when the proteins mixed with either anti-cancer drugs, siRNA, or active targeting molecules. Both in vitro and in vivo experiments indicate that our synthesized protein–drug nanoparticles (drug-loading content and encapsulation efficiency being ca. 8.2% and 70%, respectively) not only possess the capability of traditional drug delivery systems (DDS), but also have a greater drug delivery efficiency to the tumor sites and a better inhibition of tumor growth (only 35% of volume comparing to the natural growing state), indicating it being a novel drug delivery system in tumor therapy

  18. Photo-synthesis of protein-based nanoparticles and the application in drug delivery

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Jinbing; Wang, Hongyang; Cao, Yi; Qin, Meng, E-mail: qinmeng@nju.edu.cn; Wang, Wei, E-mail: wangwei@nju.edu.cn

    2015-07-15

    Recently, protein-based nanoparticles as drug delivery systems have attracted great interests due to the excellent behavior of high biocompatibility and biodegradability, and low toxicity. However, the synthesis techniques are generally costly, chemical reagents introduced, and especially present difficulties in producing homogeneous monodispersed nanoparticles. Here, we introduce a novel physical method to synthesize protein nanoparticles which can be accomplished under physiological condition only through ultraviolet (UV) illumination. By accurately adjusting the intensity and illumination time of UV light, disulfide bonds in proteins can be selectively reduced and the subsequent self-assembly process can be well controlled. Importantly, the co-assembly can also be dominated when the proteins mixed with either anti-cancer drugs, siRNA, or active targeting molecules. Both in vitro and in vivo experiments indicate that our synthesized protein–drug nanoparticles (drug-loading content and encapsulation efficiency being ca. 8.2% and 70%, respectively) not only possess the capability of traditional drug delivery systems (DDS), but also have a greater drug delivery efficiency to the tumor sites and a better inhibition of tumor growth (only 35% of volume comparing to the natural growing state), indicating it being a novel drug delivery system in tumor therapy.

  19. Multi-Temperature Zone, Droplet-based Microreactor for Increased Temperature Control in Nanoparticle Synthesis

    KAUST Repository

    Erdem, E. Yegân

    2013-12-12

    Microreactors are an emerging technology for the controlled synthesis of nanoparticles. The Multi-Temperature zone Microreactor (MTM) described in this work utilizes thermally isolated heated and cooled regions for the purpose of separating nucleation and growth processes as well as to provide a platform for a systematic study on the effect of reaction conditions on nanoparticle synthesis. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Core shell hybrids based on noble metal nanoparticles and conjugated polymers: synthesis and characterization

    Directory of Open Access Journals (Sweden)

    Battocchio Chiara

    2011-01-01

    Full Text Available Abstract Noble metal nanoparticles of different sizes and shapes combined with conjugated functional polymers give rise to advanced core shell hybrids with interesting physical characteristics and potential applications in sensors or cancer therapy. In this paper, a versatile and facile synthesis of core shell systems based on noble metal nanoparticles (AuNPs, AgNPs, PtNPs, coated by copolymers belonging to the class of substituted polyacetylenes has been developed. The polymeric shells containing functionalities such as phenyl, ammonium, or thiol pending groups have been chosen in order to tune hydrophilic and hydrophobic properties and solubility of the target core shell hybrids. The Au, Ag, or Pt nanoparticles coated by poly(dimethylpropargylamonium chloride, or poly(phenylacetylene-co-allylmercaptan. The chemical structure of polymeric shell, size and size distribution and optical properties of hybrids have been assessed. The mean diameter of the metal core has been measured (about 10-30 nm with polymeric shell of about 2 nm.

  1. Synthesis of a New Optoelectronic Material Based on Oriented Adsorption of Dyes to Nanoparticles Surface

    Institute of Scientific and Technical Information of China (English)

    LI Gui-an; SONG Jian-ping; LI Xiu

    2005-01-01

    Synthesis of the optoelectronic storage material with structure for coating by nanosized metal and azo-dye was reported. The characterization of composites was made by using transmission electron microscope (TEM), ultraviolet-visible spectrometer (UV-Vis) and thermogravity analyzer (TGA). It is found that, due to the specific structure, in which azo-dye molecules are oriented and adsorbed on the spherical surface of nanosized metal, the absorption maximum of azo-dye methyl orange shift towards shorter wavelength band. The experimental results show that the proposed technique here would offer a promising way to synthesize short wavelength optoelectronic storage material by doping of metal nanoparticles coated with dyes in polymer. Furthermore, the composites based on the structure can present excellent thermal properties suitable for the requirements of optical storage. This new type of material is capable of matching semiconductor laser (GaN) in optoelectronic storage technology.

  2. Room Temperature Co-Precipitation Synthesis of Magnetite Nanoparticles in a Large pH Window with Different Bases

    Directory of Open Access Journals (Sweden)

    Maria Cristina Mascolo

    2013-11-01

    Full Text Available Magnetite nanoparticles (Fe3O4 represent the most promising materials in medical applications. To favor high-drug or enzyme loading on the nanoparticles, they are incorporated into mesoporous materials to form a hybrid support with the consequent reduction of magnetization saturation. The direct synthesis of mesoporous structures appears to be of interest. To this end, magnetite nanoparticles have been synthesized using a one pot co-precipitation reaction at room temperature in the presence of different bases, such as NaOH, KOH or (C2H54NOH. Magnetite shows characteristics of superparamagnetism at room temperature and a saturation magnetization (Ms value depending on both the crystal size and the degree of agglomeration of individual nanoparticles. Such agglomeration appears to be responsible for the formation of mesoporous structures, which are affected by the pH, the nature of alkali, the slow or fast addition of alkaline solution and the drying modality of synthesized powders.

  3. Ultrafast laser based ``green'' synthesis of non-toxic nanoparticles in aqueous solutions

    Science.gov (United States)

    Besner, S.; Kabashin, A. V.; Winnik, F. M.; Meunier, M.

    2008-12-01

    Inorganic nanoparticles offer novel promising properties for biological sensing and imaging, as well as in therapeutics. However, these applications are often complicated by the possible toxicity of conventional nanomaterials, arising as a result of inadequate purification procedures of nanoparticles obtained via synthetic pathways using toxic or non-biocompatible substances. We review novel femtosecond laser-assisted methods, which enable the preparation of metal nanomaterials in clean, biologically friendly aqueous environment (“green” synthesis) and thus completely solve the toxicity problem. The proposed methods, including laser ablation and fragmentation, make possible the production of stable metal colloids of extremely small size (˜2 nm) with a low coefficient of variation (15-25%). Those nanoparticles exhibit unique surface chemistry and can be used for bio-imaging, cancer treatment and nanoparticle-enhanced Raman spectroscopy.

  4. Synthesis, characterization and functionalization of silicon nanoparticle based hybrid nanomaterials for photovoltaic and biological applications

    Science.gov (United States)

    Xu, Zejing

    Silicon nanoparticles are attractive candidates for biological, photovoltaic and energy storage applications due to their size dependent optoelectronic properties. These include tunable light emission, high brightness, and stability against photo-bleaching relative to organic dyes (see Chapter 1). The preparation and characterization of silicon nanoparticle based hybrid nanomaterials and their relevance to photovoltaic and biological applications are described. The surface-passivated silicon nanoparticles were produced in one step from the reactive high-energy ball milling (RHEBM) of silicon wafers with various organic ligands. The surface structure and optical properties of the passivated silicon nanoparticles were systematically characterized. Fast approaches for purifying and at the same time size separating the silicon nanoparticles using a gravity GPC column were developed. The hydrodynamic diameter and size distribution of these size-separated silicon nanoparticles were determined using GPC and Diffusion Ordered NMR Spectroscopy (DOSY) as fast, reliable alternative approaches to TEM. Water soluble silicon nanoparticles were synthesized by grafting PEG polymers onto functionalized silicon nanoparticles with distal alkyne or azide moieties. The surface-functionalized silicon nanoparticles were produced from the reactive high-energy ball milling (RHEBM) of silicon wafers with a mixture of either 5-chloro-1-pentyne in 1-pentyne or 1,7 octadiyne in 1-hexyne to afford air and water stable chloroalkyl or alkynyl terminated nanoparticles, respectively. Nanoparticles with the ω-chloroalkyl substituents were easily converted to ω-azidoalkyl groups through the reaction of the silicon nanoparticles with sodium azide in DMF. The azido terminated nanoparticles were then grafted with monoalkynyl-PEG polymers using a copper catalyzed alkyne-azide cycloaddition (CuAAC) reaction to afford core-shell silicon nanoparticles with a covalently attached PEG shell. Covalently

  5. Controlled Synthesis of CuO Nanoparticles by TritonX-100-based Microemulsions

    Institute of Scientific and Technical Information of China (English)

    SHEN Changbin; CHEN Yin

    2014-01-01

    CuO nanoparticles were synthesized by using microreactors made of Triton X-100/n-hextnol/cyclohexane/water W/O microemulsion system. Basic synthesis parameters were determined. The results of thermo gravimetric/differential thermal analysis (TG/DTA) of the precursor products indicated that the proper calcination temperature was about 500℃. The nanoparticles were characterized by X-ray diffraction(XRD), transmission electron microscopy (TEM) and UV-visible spectra. It was indicated that the grain size was highly dependent on the ratio of water to surfactant(R). With the R value increasing, the particles size became larger.

  6. Synthesis of colloids based on gold nanoparticles dispersed in castor oil

    International Nuclear Information System (INIS)

    New colloidal solutions of gold nanoparticles (AuNP), using castor oil as a nontoxic organic dispersant agent, were prepared via three different methods. In all three cases, tetrachloroauric(III) acid was employed as the gold source. The colloids were characterized by UV-Vis spectroscopy and transmission electron microscopy (TEM). The AuNP produced by the three methods were quasispherical in shape, however with different average sizes. The individual characteristics of the nanoparticles presented in each colloidal system were also confirmed by observation of absorption maxima at different wavelengths of visible light. Each method of synthesis leads to colloids with different grades of stability with respect to particle agglomeration.

  7. Magnetoliposomes based on nickel/silica core/shell nanoparticles: Synthesis and characterization

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, Ana Rita O.; Gomes, I.T.; Almeida, Bernardo G. [Centro de Física (CFUM), Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Araújo, J.P. [IFIMUP/IN – Instituto de Nanociência e Nanotecnologia, R. Campo Alegre, 4169-007 Porto (Portugal); Castanheira, Elisabete M.S. [Centro de Física (CFUM), Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Coutinho, Paulo J.G., E-mail: pcoutinho@fisica.uminho.pt [Centro de Física (CFUM), Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal)

    2014-12-15

    In the present work, nickel magnetic nanoparticles with diameters lower than 100 nm, with and without silica shell, were synthesized by microheterogeneous templating. The magnetic properties of the nanoparticles show a typical ferromagnetic behavior with a coercive field of 80 Oe. Dry magnetoliposomes (DMLs) with diameter between 58 nm and 76 nm were obtained from the synthesis of nanoparticles in the presence of a lipid or surfactant layer, and aqueous magnetoliposomes (AMLs) were obtained by encapsulation of the nanoparticles in liposomes. FRET (Förster resonance energy transfer) experiments were performed to study the non-specific interactions between aqueous magnetoliposomes and giant unilamellar vesicles (GUVs), as models of cell membranes. It was possible to detect membrane fusion between GUVs and AMLs containing both NBD-C{sub 6}-HPC (donor) and the dye Nile Red (acceptor). - Highlights: • Magnetic nickel nanoparticles were synthesized in microheterogeneous media. • The nanoparticles were covered with a silica shell to improve biocompatibility. • Aqueous and dry magnetoliposomes were prepared, the latter with diameter around 70 nm. • Membrane fusion between magnetoliposomes and models of cell membranes was detected by FRET.

  8. Synthesis of chitosan based nanoparticles and their in vitro evaluation against phytopathogenic fungi.

    Science.gov (United States)

    Saharan, Vinod; Mehrotra, Akanksha; Khatik, Rajesh; Rawal, Pokhar; Sharma, S S; Pal, Ajay

    2013-11-01

    The main aim of present study was to prepare chitosan, chitosan-saponin and Cu-chitosan nanoparticles to evaluate their in vitro antifungal activities. Various nanoparticles were prepared using ionic gelation method by interaction of chitosan, sodium tripolyphosphate, saponin and Cu ions. Their particle size, polydispersity index, zeta potential and structures were confirmed by DLS, FTIR, TEM and SEM. The antifungal properties of nanoparticles against phytopathogenic fungi namely Alternaria alternata, Macrophomina phaseolina and Rhizoctonia solani were investigated at various concentrations ranging from 0.001 to 0.1%. Among the various formulations of nanoparticles, Cu-chitosan nanoparticles were found most effective at 0.1% concentration and showed 89.5, 63.0 and 60.1% growth inhibition of A. alternata, M. phaseolina and R. solani, respectively in in vitro model. At the same concentration, Cu-chitosan nanoparticles also showed maximum of 87.4% inhibition rate of spore germination of A. alternata. Chitosan nanoparticles showed the maximum growth inhibitory effects (87.6%) on in vitro mycelial growth of M. phaseolina at 0.1% concentration. From our study it is evident that chitosan based nanoparticles particularly chitosan and Cu-chitosan nanoparticles have tremendous potential for further field screening towards crop protection.

  9. Solventless synthesis of ruthenium nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    García-Peña, Nidia G. [Departmento de Tecnociencias, Universidad Nacional Autónoma de México, Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México, Cd. Universitaria A.P. 70-186, C.P. 04510 Coyoacán, México D.F. (Mexico); Redón, Rocío, E-mail: rredon@unam.mx [Departmento de Tecnociencias, Universidad Nacional Autónoma de México, Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México, Cd. Universitaria A.P. 70-186, C.P. 04510 Coyoacán, México D.F. (Mexico); Herrera-Gomez, Alberto [Estudios Avanzados del Instituto Politécnico Nacional, Campus Juriquilla, Querétaro (Mexico); Fernández-Osorio, Ana Leticia [FES-Cuautitlán, Universidad Nacional Autónoma de México, Edo. de Mexico (Mexico); Bravo-Sanchez, Mariela; Gomez-Sosa, Gustavo [Estudios Avanzados del Instituto Politécnico Nacional, Campus Juriquilla, Querétaro (Mexico)

    2015-06-15

    Graphical abstract: - Highlights: • Successful synthesis of Ru nanoparticles by a cheap, fast and solventless approach was achieved. • The zero-valent state as well as the by-product/impurity free of the mechanochemical obtained Ru nanoparticles was proven by XPS, TEM and XRD. • Compared to two other synthesis strategies, the above-mentioned synthesis was more suitable to obtain smaller particles with fewer impurities in shorter time. - Abstract: This paper presents a novel solventless method for the synthesis of zero-valent ruthenium nanoparticles Ru(0). The proposed method, although not entirely new in the nanomaterials world, was used for the first time to synthesize zero-valent ruthenium nanoparticles. This new approach has proved to be an environmentally friendly, clean, cheap, fast, and reproducible technique which employs low amounts of solvent. It was optimized through varying amounts of reducing salt on a determined quantity of precursor and measuring the effect of this variation on the average particle size obtained. The resulting products were fully characterized by powder XRD, TEM, HR-TEM, and XPS studies, all of which corroborated the purity of the nanoparticles achieved. In order to verify the advantages of our method over other techniques, we compared our nanoparticles with two common colloidal-synthesized ruthenium nanoparticles.

  10. Nano composites Based on Technical Polymers and Sterically Functionalized Soft Magnetic Magnetite Nanoparticles: Synthesis, Processing, and Characterization

    International Nuclear Information System (INIS)

    This experimental study deals with the synthesis, processing, and characterization of highly filled nano composites based on polyvinyl butyral/magnetite (PVB/Fe3O4) and polymethylmethacrylate /magnetite (PMMA/Fe3O4). The nanoparticles are synthesized in an aqueous coprecipitation reaction and show a single particle diameter of approximately 15 nm. The particles are sterically functionalized and covered by PVB and PMMA in a spray drying process. The synthesized compound particles are further processed by injection molding to test specimens with filler contents up to 14.5 vol.-%. PVB and PMMA specimen are processed as a reference as well. The distribution of the nanoparticles is characterized by microscopy. Besides a minor number of agglomerates and aggregates the nanoparticles are distributed homogeneously in the PVB composites. Furthermore, the injection molded specimens are characterized with regard to their thermal degradation, polymer structure, and their mechanical and magnetic properties. The presence of nanoparticles capped with ricinoleic acid shows significant decrease in degradation temperature and in glass transition temperature of PVB. The degradation temperature of PMMA is increased by adding nanoparticles capped with oleic acid. Dynamic-mechanical properties as well as the magnetic permeability of PVB and PMMA are improved significantly by adding nanoparticles

  11. Green chemistry for nanoparticle synthesis.

    Science.gov (United States)

    Duan, Haohong; Wang, Dingsheng; Li, Yadong

    2015-08-21

    The application of the twelve principles of green chemistry in nanoparticle synthesis is a relatively new emerging issue concerning the sustainability. This field has received great attention in recent years due to its capability to design alternative, safer, energy efficient, and less toxic routes towards synthesis. These routes have been associated with the rational utilization of various substances in the nanoparticle preparations and synthetic methods, which have been broadly discussed in this tutorial review. This article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present several pivotal aspects of synthesis with environmental concerns, involving the selection and evaluation of nontoxic capping and reducing agents, the choice of innocuous solvents and the development of energy-efficient synthetic methods.

  12. Green chemistry for nanoparticle synthesis.

    Science.gov (United States)

    Duan, Haohong; Wang, Dingsheng; Li, Yadong

    2015-08-21

    The application of the twelve principles of green chemistry in nanoparticle synthesis is a relatively new emerging issue concerning the sustainability. This field has received great attention in recent years due to its capability to design alternative, safer, energy efficient, and less toxic routes towards synthesis. These routes have been associated with the rational utilization of various substances in the nanoparticle preparations and synthetic methods, which have been broadly discussed in this tutorial review. This article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present several pivotal aspects of synthesis with environmental concerns, involving the selection and evaluation of nontoxic capping and reducing agents, the choice of innocuous solvents and the development of energy-efficient synthetic methods. PMID:25615873

  13. Synthesis and thermal behavior of tin-based alloy (Sn-Ag-Cu) nanoparticles.

    Science.gov (United States)

    Roshanghias, Ali; Yakymovych, Andriy; Bernardi, Johannes; Ipser, Herbert

    2015-03-19

    The prominent melting point depression of nanoparticles has been the subject of a considerable amount of research. For their promising applications in electronics, tin-based nano-alloys such as near-eutectic Sn-Ag-Cu (SAC) alloys have been synthesized via various techniques. However, due to issues such as particle aggregation and oxidation or introduced impurities, the application of these nano-size particles has been confined or aborted. For instance, thermal investigations by DTA/DSC in a large number of studies revealed exothermic peaks in the range of 240-500 °C, i.e. above the melting point of SAC nanoparticles, with different and quite controversial explanations for this unclear phenomenon. This represents a considerable drawback for the application of nanoparticles. Correspondingly, in the current study, the thermal stability of SAC nanoparticles has been investigated via electron microscopy, XRD, FTIR, and DSC/TG analysis. It was found that the nanoparticles consist mainly of a metallic β-Sn core and an amorphous tin hydroxide shell structure. The SnO crystalline phase formation from this amorphous shell has been associated with the exothermic peaks on the first heating cycle of the nanoparticles, followed by a disproportionation reaction into metallic Sn and SnO₂.The results also revealed that the surfactant and reducing agent cannot only affect the size and size distribution of the nanoparticles, they might also alter the ratio between the amorphous shell and the crystalline core in the structure of particles. PMID:25757694

  14. Synthesis and characterization of titania-based monodisperse fluorescent europium nanoparticles for biolabeling

    Energy Technology Data Exchange (ETDEWEB)

    Tan Mingqian [Department of Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Dalian 116023 (China); Wang Guilan [Department of Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Dalian 116023 (China); Ye Zhiqiang [Department of Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Dalian 116023 (China); Yuan Jingli [Department of Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Dalian 116023 (China)]. E-mail: jingliyuan@yahoo.com.cn

    2006-03-15

    Inorganic-organic hybrid titania-based nanoparticles covalently bound to a fluorescent Eu{sup 3+} chelate of 4,4'-bis(1'',1'',1'',2'',2'',3'',3''-heptafluoro-4'',6''-hexanedion-6''-yl) chlorosulfo-o-terphenyl (BHHCT-Eu{sup 3+}) were synthesized by a sol-gel technique. A conjugate of BHHCT with 3-[2-(2-aminoethylamino) ethylamino]propyl-trimethoxysilane (APTS) was used as a precursor for the nanoparticle preparation and monodisperse nanoparticles consisting of titania network and silica sub-network covalently bound to the Eu{sup 3+} chelate were prepared by the copolymerization of APTS-BHHCT conjugate, titanium tetraisopropoxide (TTIP) and free APTS in EuCl{sub 3} water-alcohol solution. The effects of reaction conditions on size and fluorescence lifetime of the nanoparticles were investigated. The characterizations by transmission electron microscopy and fluorometric methods indicate that the nanoparticles are near spherical and strongly fluorescent having a fluorescence quantum yield of 11.6% and a long fluorescence lifetime of {approx}0.4 ms. The direct-introduced amino groups on the nanoparticle's surface by using free APTS in nanoparticle preparation facilitated the biolabeling process of the nanoparticles. The nanoparticle-labeled streptavidin (SA) was prepared and used in a sandwich-type time-resolved fluoroimmunoassay (TR-FIA) of human prostate-specific antigen (PSA) by using a 96-well microtiter plate as the solid phase carrier. The method gives a detection limit of 66 pg/ml for the PSA assay.

  15. Nanoparticle synthesis for magnetic hyperthermia

    OpenAIRE

    Thomas, L

    2010-01-01

    This work reports on an investigation into the synthesis, control, and stabilisation of iron oxide nanoparticles for biomedical applications using magnetic hyperthermia. A new understanding of the factors effecting nanoparticle growth in a coprecipitation methodology has been determined. This thesis challenges the highly cited Ostwald Ripening as the primary mechanism for nanoparticulate growth, and instead argues that in certain conditions, such as increasing reaction tempe...

  16. Quaternized Carboxymethyl Chitosan-Based Silver Nanoparticles Hybrid: Microwave-Assisted Synthesis, Characterization and Antibacterial Activity

    Directory of Open Access Journals (Sweden)

    Siqi Huang

    2016-06-01

    Full Text Available A facile, efficient, and eco-friendly approach for the preparation of uniform silver nanoparticles (Ag NPs was developed. The synthesis was conducted in an aqueous medium exposed to microwave irradiation for 8 min, using laboratory-prepared, water-soluble quaternized carboxymethyl chitosan (QCMC as a chemical reducer and stabilizer and silver nitrate as the silver source. The structure of the prepared QCMC was characterized using Fourier transform infrared (FT-IR and 1H nuclear magnetic resonance (NMR. The formation, size distribution, and dispersion of the Ag NPs in the QCMC matrix were determined using X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, ultraviolet-visible (UV-Vis, transmission electron microscopy (TEM, and field emission scanning electron microscope (FESEM analysis, and the thermal stability and antibacterial properties of the synthesized QCMC-based Ag NPs composite (QCMC-Ag were also explored. The results revealed that (1 QCMC was successfully prepared by grafting quaternary ammonium groups onto carboxymethyl chitosan (CMC chains under microwave irradiation in water for 90 min and this substitution appeared to have occurred at -NH2 sites on C2 position of the pyranoid ring; (2 uniform and stable spherical Ag NPs could be synthesized when QCMC was used as the reducing and stabilizing agent; (3 Ag NPs were well dispersed in the QCMC matrix with a narrow size distribiution in the range of 17–31 nm without aggregation; and (4 due to the presence of Ag NPs, the thermal stability and antibacterial activity of QCMC-Ag were dramatically improved relative to QCMC.

  17. Solventless synthesis of ruthenium nanoparticles

    Science.gov (United States)

    García-Peña, Nidia G.; Redón, Rocío; Herrera-Gomez, Alberto; Fernández-Osorio, Ana Leticia; Bravo-Sanchez, Mariela; Gomez-Sosa, Gustavo

    2015-06-01

    This paper presents a novel solventless method for the synthesis of zero-valent ruthenium nanoparticles Ru(0). The proposed method, although not entirely new in the nanomaterials world, was used for the first time to synthesize zero-valent ruthenium nanoparticles. This new approach has proved to be an environmentally friendly, clean, cheap, fast, and reproducible technique which employs low amounts of solvent. It was optimized through varying amounts of reducing salt on a determined quantity of precursor and measuring the effect of this variation on the average particle size obtained. The resulting products were fully characterized by powder XRD, TEM, HR-TEM, and XPS studies, all of which corroborated the purity of the nanoparticles achieved. In order to verify the advantages of our method over other techniques, we compared our nanoparticles with two common colloidal-synthesized ruthenium nanoparticles.

  18. Synthesis and catalytic application of palladium nanoparticles supported on kaolinite-based nanohybrid materials.

    Science.gov (United States)

    Ngnie, Gaelle; Dedzo, Gustave K; Detellier, Christian

    2016-05-31

    Palladium nanoparticles (PdNPs) were deposited on the surface of the modified clay mineral, kaolinite. To improve compatibility, abundance and control of the size of the nanoparticles, kaolinite was modified by the grafting of an amino alcohol (triethanolamine (TEA)) and an ionic liquid (1-(2-hydroxyethyl)-3-methylimidazolium (ImIL)). Characterization techniques (XRD, TGA, solid state (13)C NMR and FTIR spectroscopy) confirmed the effective grafting of these compounds on the internal surface of kaolinite. After the synthesis of PdNPs onto clay particles, TEM allowed the visualization of abundant PdNPs with sizes ranging from 4 to 6 nm, uniformly distributed onto the platelets of modified kaolinite. Unmodified clay showed low abundance and random distribution of the nanoparticles. The catalysts obtained were effective for the catalytic reduction of 4-nitrophenol (4-NP), the material with TEA being the most effective. These materials have exhibited excellent performance during the Heck and particularly the Suzuki-Miyaura coupling reactions, with reaction yields up to 100%. These catalysts showed a very slight loss in activity for three consecutive catalytic cycles (less than 10% decrease of the activity compared to the first cycle). This was an evidence that the prior grafting modification of kaolinite helps in significantly improving the quality of the synthesized NPs and also promotes their strong attachment onto the clay mineral surface. PMID:27160392

  19. Synthesis of copper/nickel nanoparticles using newly synthesized Schiff-base metals complexes and their cytotoxicity/catalytic activities.

    Science.gov (United States)

    Aazam, Elham S; El-Said, Waleed Ahmed

    2014-12-01

    Transition metal complexes compounds with Schiff bases ligand representing an important class of compounds that could be used to develop new metal-based anticancer agents and as precursors of metal NPs. Herein, 2,3-bis-[(3-ethoxy-2-hydroxybenzylidene)amino]but-2-enedinitrile Schiff base ligand and its corresponding copper/nickel complexes were synthesized. Also, we reported a facile and rapid method for synthesis nickel/copper nanoparticles based on thermal reduction of their complexes. Free ligand, its metal complexes and metals nanoparticles have been characterized based on elemental analysis, transmission electron microscopy, powder X-ray diffraction, magnetic measurements and by various spectroscopic (UV-vis, FT-IR, (1)H NMR, GC-MS) techniques. Additionally, the in vitro cytotoxic activity of free ligand and its complexes compounds were assessed against two cancer cell lines (HeLa and MCF-7 cells)and one healthy cell line (HEK293 cell). The copper complex was found to be active against these cancer cell lines at very low LD50 than the free ligand, while nickel complex did not show any anticancer activity against these cell lines. Also, the antibacterial activity of as-prepared copper nanoparticles were screened against Escherichia coli, which demonstrated minimum inhibitory concentration and minimum bactericidal concentration values lower than those values of the commercial Cu NPs as well as the previous reported values. Moreover, the synthesized nickel nanoparticles demonstrated remarkable catalytic performance toward hydrogenation of nitrobenzene that producing clean aniline with high selectivity (98%). This reactivity could be attributed to the high degree of dispersion of Ni nanoparticles.

  20. Microwave synthesis of zirconia nanoparticles.

    Science.gov (United States)

    Hembram, K P S S; Rao, G Mohan

    2008-08-01

    Zirconia nanoparticles were prepared by microwave synthesis from zirconium acetate hydroxide. The samples were characterized by various techniques like X-ray diffraction (XRD), Scanning Electron microscopy (SEM), Transmission Electron microscopy (TEM), Raman Spectroscopy (RS). By XRD the average crystallite size is obtained around 10 nm and which is comparable to observation by SEM and TEM. PMID:19049194

  1. A synthesis of fluorescent starch based on carbon nanoparticles for fingerprints detection

    Science.gov (United States)

    Li, Hongren; Guo, Xingjia; Liu, Jun; Li, Feng

    2016-10-01

    A pyrolysis method for synthesizing carbon nanoparticles (CNPs) were developed by using malic acid and ammonium oxalate as raw materials. The incorporation of a minor amount of carbon nanoparticles into starch powder imparts remarkable color-tunability. Based on this phenomenon, an environment friendly fluorescent starch powder for detecting latent fingerprints in non-porous surfaces was prepared. The fingerprints on different non-porous surfaces developed with this powder showed very good fluorescent images under ultraviolet excitation. The method using fluorescent starch powder as fluorescent marks is simple, rapid and green. Experimental results illustrated the effectiveness of proposed methods, enabling its practical applications in forensic sciences.

  2. Synthesis of methylprednisolone loaded ibuprofen modified inulin based nanoparticles and their application for drug delivery.

    Science.gov (United States)

    Zhang, Luzhong; Li, Yue; Wang, Caiping; Li, Guicai; Zhao, Yahong; Yang, Yumin

    2014-09-01

    Ibuprofen modified inulin was synthesized through a direct esterification linkage in which the in situ activation of the carboxylic acid with N,N'-carbonyldiimidazole was carried out. The critical aggregation concentration of the ibuprofen modified inulin was determined by using pyrene as the fluorescence probe. Methylprednisolone loaded nanoparticles were prepared by the self-assembly of the ibuprofen modified inulin copolymer and methylprednisolone. In vitro release of the methylprednisolone and the cytotoxicity of the methylprednisolone loaded nanoparticles against RSC-96 cells were evaluated. Since the ibuprofen and methylprednisolone could stimulate a significant neurite growth and diminish the human neurological deficits after the spinal cord injury, the methylprednisolone loaded nanoparticles based on the ibuprofen modified inulin copolymer may have a great potential in the synergetic effect treatment for spinal cord injury.

  3. Synthesis of PEG-PCL-based polyurethane nanoparticles by miniemulsion polymerization.

    Science.gov (United States)

    Valério, Alexsandra; Conti, Denise S; Araújo, Pedro H H; Sayer, Claudia; da Rocha, Sandro R P

    2015-11-01

    In this work biocompatible polyurethane nanoparticles for future application as noninvasive polymeric nanocarriers using propellant-based inhalers in the treatment of respiratory diseases were prepared by miniemulsion interfacial polymerization derived from isophorone diisocyanate, poly(ϵ-caprolactone), and poly(ethylene glycol). The effects of the surfactant type, nonionic Tween 80 and Brij 35, anionic sodium dodecyl sulfate, and cationic cetyltrimethyl ammonium bromide, and poly(ethylene glycol) molar mass on the stability, size and morphology of nanoparticles were evaluated. In addition, the ability of cells to proliferate in contact with polyurethane nanoparticles was assessed by MTS ([(3-(4,5-dimethylthiazole-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfo-phenyl)-2H-tetrazolium, inner salt]) assay using human lung adenocarcinoma A549 cells, an in vitro model of Type II alveolar epithelium.

  4. Lactobacillus assisted synthesis of titanium nanoparticles

    Science.gov (United States)

    Prasad, K.; Jha, Anal K.; Kulkarni, A. R.

    2007-05-01

    An eco-friendly lactobacillus sp. (microbe) assisted synthesis of titanium nanoparticles is reported. The synthesis is performed at room temperature. X-ray and transmission electron microscopy analyses are performed to ascertain the formation of Ti nanoparticles. Individual nanoparticles as well as a number of aggregates almost spherical in shape having a size of 40 60 nm are found.

  5. Green Chemistry Techniques for Gold Nanoparticles Synthesis

    Science.gov (United States)

    Cannavino, Sarah A.; King, Christy A.; Ferrara, Davon W.

    Gold nanoparticles (AuNPs) are often utilized in many technological and research applications ranging from the detection of tumors, molecular and biological sensors, and as nanoantennas to probe physical processes. As these applications move from the research laboratory to industrial settings, there is a need to develop efficient and sustainable synthesis techniques. Recent research has shown that several food products and beverages containing polyphenols, a common antioxidant, can be used as reducing agents in the synthesis of AuNPs in solution. In this study, we explore a variety of products to determine which allow for the most reproducible solution of nanoparticles based on the size and shapes of particles present. We analyzed the AuNPs solutions using extinction spectroscopy and atomic force microscopy. We also develop a laboratory activity to introduce introductory chemistry and physics students to AuNP synthesis techniques and analysis.

  6. Synthesis and characterization of CuO nanoparticles using strong base electrolyte through electrochemical discharge process

    Indian Academy of Sciences (India)

    PURUSHOTTAM KUMAR SINGH; PANKAJ KUMAR; MANOWAR HUSSAIN; ALOK KUMAR DAS; GANESH CHANDRA NAYAK

    2016-04-01

    In the present study, cupric oxide (CuO) nanoparticles were synthesized by electrochemical discharge process using strong base electrolytes. The experiments were carried out separately using NaOH and KOH electrolytes.The mass output rate and the crystal size were obtained with variation of the rotation speed of magnetic stirrer for both types of electrolytes. The mass output rate of CuO nanoparticles increased with the increase in the speed of rotation, and, after an optimum speed, it started decreasing. However, the size of the particles reduced with the increase of the rotation speed. The crystal plane of the obtained CuO nanoparticles was similar for both the electrolytes whereas the yield of nanoparticles was higher in KOH as compared with NaOH under the sameexperiment conditions. In this set of experiments, the maximum output rates obtained were 21.66 mg h$^{−1}$ for NaOH and 24.66 mg h$^{−1}$ for KOH at 200 rpm for a single discharge arrangement. The average crystal size of CuO particles obtained was in the range of 13–18 nm for KOH electrolyte and 15–20 nm for NaOH electrolyte. Scanning electron microscopy images revealed that flower-like and caddice clew-shaped CuO nanocrystalline particles weresynthesized by the electrochemical discharge process. Fourier transform infrared spectrum showed that the CuO nanoparticles have a pure and monolithic phase. UV–vis–NIR spectroscopy was used to monitor oxidation course of Cu→CuO and the band gap energy was measured as 2 and 2.6 eV for CuO nanoparticle synthesized in NaOH and KOH solutions, respectively.

  7. Room temperature synthesis of Ni-based alloy nanoparticles by radiolysis.

    Energy Technology Data Exchange (ETDEWEB)

    Nenoff, Tina Maria; Berry, Donald T.; Lu, Ping; Leung, Kevin; Provencio, Paula Polyak; Stumpf, Roland Rudolph; Huang, Jian Yu; Zhang, Zhenyuan

    2009-09-01

    Room temperature radiolysis, density functional theory, and various nanoscale characterization methods were used to synthesize and fully describe Ni-based alloy nanoparticles (NPs) that were synthesized at room temperature. These complementary methods provide a strong basis in understanding and describing metastable phase regimes of alloy NPs whose reaction formation is determined by kinetic rather than thermodynamic reaction processes. Four series of NPs, (Ag-Ni, Pd-Ni, Co-Ni, and W-Ni) were analyzed and characterized by a variety of methods, including UV-vis, TEM/HRTEM, HAADF-STEM and EFTEM mapping. In the first focus of research, AgNi and PdNi were studied. Different ratios of Ag{sub x}- Ni{sub 1-x} alloy NPs and Pd{sub 0.5}- Ni{sub 0.5} alloy NP were prepared using a high dose rate from gamma irradiation. Images from high-angle annular dark-field (HAADF) show that the Ag-Ni NPs are not core-shell structure but are homogeneous alloys in composition. Energy filtered transmission electron microscopy (EFTEM) maps show the homogeneity of the metals in each alloy NP. Of particular interest are the normally immiscible Ag-Ni NPs. All evidence confirmed that homogeneous Ag-Ni and Pd-Ni alloy NPs presented here were successfully synthesized by high dose rate radiolytic methodology. A mechanism is provided to explain the homogeneous formation of the alloy NPs. Furthermore, studies of Pd-Ni NPs by in situ TEM (with heated stage) shows the ability to sinter these NPs at temperatures below 800 C. In the second set of work, CoNi and WNi superalloy NPs were attempted at 50/50 concentration ratios using high dose rates from gamma irradiation. Preliminary results on synthesis and characterization have been completed and are presented. As with the earlier alloy NPs, no evidence of core-shell NP formation occurs. Microscopy results seem to indicate alloying occurred with the CoNi alloys. However, there appears to be incomplete reduction of the Na{sub 2}WO{sub 4} to form the W

  8. Gelatin-based nanoparticles as DNA delivery systems: Synthesis, physicochemical and biocompatible characterization.

    Science.gov (United States)

    Morán, M C; Rosell, N; Ruano, G; Busquets, M A; Vinardell, M P

    2015-10-01

    The rapidly rising demand for therapeutic grade DNA molecules requires associated improvements in encapsulation and delivery technologies. One of the challenges for the efficient intracellular delivery of therapeutic biomolecules after their cell internalization by endocytosis is to manipulate the non-productive trafficking from endosomes to lysosomes, where degradation may occur. The combination of the endosomal acidity with the endosomolytic capability of the nanocarrier can increase the intracellular delivery of many drugs, genes and proteins, which, therefore, might enhance their therapeutic efficacy. Among the suitable compounds, the gelification properties of gelatin as well as the strong dependence of gelatin ionization with pH makes this compound an interesting candidate to be used to the effective intracellular delivery of active biomacromolecules. In the present work, gelatin (either high or low gel strength) and protamine sulfate has been selected to form particles by interaction of oppositely charged compounds. Particles in the absence of DNA (binary system) and in the presence of DNA (ternary system) have been prepared. The physicochemical characterization (particle size, polydispersity index and degree of DNA entrapment) have been evaluated. Cytotoxicity experiments have shown that the isolated systems and the resulting gelatin-based nanoparticles are essentially non-toxic. The pH-dependent hemolysis assay and the response of the nanoparticles co-incubated in buffers at defined pHs that mimic extracellular, early endosomal and late endo-lysosomal environments demonstrated that the nanoparticles tend to destabilize and DNA can be successfully released. It was found that, in addition to the imposed compositions, the gel strength of gelatin is a controlling parameter of the final properties of these nanoparticles. The results indicate that these gelatin-based nanoparticles have excellent properties as highly potent and non-toxic intracellular delivery

  9. In Situ Synthesis of Metal Sulfide Nanoparticles Based on 2D Metal-Organic Framework Nanosheets.

    Science.gov (United States)

    Lu, Qipeng; Zhao, Meiting; Chen, Junze; Chen, Bo; Tan, Chaoliang; Zhang, Xiao; Huang, Ying; Yang, Jian; Cao, Feifei; Yu, Yifu; Ping, Jianfeng; Zhang, Zhicheng; Wu, Xue-Jun; Zhang, Hua

    2016-09-01

    A facile in situ synthetic method is developed to synthesize metal sulfide nanoparticles based on 2D M-TCPP (M = Cu, Cd, or Co, TCPP = tetrakis(4-carboxyphenyl)porphyrin)) metal-organic framework nanosheets. The obtained CuS/Cu-TCPP composite nanosheet is used as the active material in photoelectrochemical cells, showing notably increased photocurrent due to the improved exciton separation and charge carrier transport.

  10. SYNTHESIS OF COPPER NANOPARTICLES BY ASPERGILLUS SPECIES

    Directory of Open Access Journals (Sweden)

    Kantabathini Venkata Pavani

    2013-06-01

    Full Text Available Recent developments in the biosynthesis of nanomaterials have demonstrated the important role of microorganisms in nanotechnology. The organisms show a unique potential in environmentally friendly production and accumulation of nanoparticles with different shapes and sizes. The present study proposed a green process for synthesis of copper nanoparticles using Aspergillus species. Syntheses of copper nanoparticles were characterized by UV-visible spectroscopy. The extracellular synthesis of copper nanoparticles was characterized by scanning electron microscopy and Transmission electron microscopy.

  11. Fast and facile preparation of CTAB based gels and their applications in Au and Ag nanoparticles synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Upadhyay, Ravi Kant, E-mail: rkupadhyay85@gmail.com [Department of Chemistry, School of Natural Sciences, Shiv Nadar University, Gautam Budh Nagar, 201314 Uttar Pradesh (India); Soin, Navneet, E-mail: n.soin@bolton.ac.uk [Knowledge Centre for Materials Chemistry (KCMC), Institute for Materials Research and Innovation (IMRI), University of Bolton, Deane Road, Bolton BL3 5AB (United Kingdom); Saha, Susmita, E-mail: ssaha@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Barman, Anjan, E-mail: abarman@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Sinha Roy, Susanta, E-mail: susanta.roy@snu.edu.in [Department of Physics, School of Natural Sciences, Shiv Nadar University, Gautam Budh Nagar, 201314 Uttar Pradesh (India)

    2015-04-15

    We have demonstrated that the gel-like mesophase of Cetyltrimethylammonium bromide (CTAB) can be synthesized by judicial adjustment of water to surfactant molar ratio (W{sub 0}), without using any additional salts, gelating agents or co-surfactants. Gel formation was found to be highly dependent on the water to surfactant molar ratio (W{sub 0}), with the lowest value of W{sub 0} (41.5) resulting in rapid gel formation. Environmental scanning electron microscope (ESEM) analysis revealed that the gel was comprised of interconnected cylindrical structures. The presence of hydrogen bonding in the gel-like mesophase was confirmed by Fourier Transform Infrared spectroscopy (FTIR) analysis. Rheology measurements revealed that all the gel samples were highly viscoelastic in nature. Furthermore, Au and Ag containing CTAB gels were explored as precursors for the preparation of spherical Gold (Au) and Silver (Ag) nanoparticles using Sodium borohydride (NaBH{sub 4}) as reducing agent. The effects of NaBH{sub 4} concentration on the particle size and morphology of the Au and Ag nanoparticles have also been studied. - Highlights: • A facile synthesis of CTAB based gel-like mesophase is reported. • CTAB gels were obtained by adjusting water to surfactant molar ratio (W{sub 0}). • FTIR analysis revealed that hydrogen bonding plays a key role in gel formation. • Au, Ag nanoparticles were synthesized by using CTAB gel and NaBH{sub 4}.

  12. Fast and facile preparation of CTAB based gels and their applications in Au and Ag nanoparticles synthesis

    International Nuclear Information System (INIS)

    We have demonstrated that the gel-like mesophase of Cetyltrimethylammonium bromide (CTAB) can be synthesized by judicial adjustment of water to surfactant molar ratio (W0), without using any additional salts, gelating agents or co-surfactants. Gel formation was found to be highly dependent on the water to surfactant molar ratio (W0), with the lowest value of W0 (41.5) resulting in rapid gel formation. Environmental scanning electron microscope (ESEM) analysis revealed that the gel was comprised of interconnected cylindrical structures. The presence of hydrogen bonding in the gel-like mesophase was confirmed by Fourier Transform Infrared spectroscopy (FTIR) analysis. Rheology measurements revealed that all the gel samples were highly viscoelastic in nature. Furthermore, Au and Ag containing CTAB gels were explored as precursors for the preparation of spherical Gold (Au) and Silver (Ag) nanoparticles using Sodium borohydride (NaBH4) as reducing agent. The effects of NaBH4 concentration on the particle size and morphology of the Au and Ag nanoparticles have also been studied. - Highlights: • A facile synthesis of CTAB based gel-like mesophase is reported. • CTAB gels were obtained by adjusting water to surfactant molar ratio (W0). • FTIR analysis revealed that hydrogen bonding plays a key role in gel formation. • Au, Ag nanoparticles were synthesized by using CTAB gel and NaBH4

  13. Applied synthesis and characterisation of nanoparticles

    OpenAIRE

    Bear, J C

    2014-01-01

    This thesis covers three areas of development of nanomaterials synthesis; namely the synthesis of superhydrophobic polymer-nanoparticle composites (chapter 3), the synthesis of doped quantum dots for catalysis and photoluminescence enhancement (chapter 4) and the synthesis of magnetic iron oxide nanoparticles from inexpensive, readily available reagents (chapter 5). Details of characterisation and analytical techniques and synthetic methods used are given in chapter 2, and the thesis summaris...

  14. Phase diagrams of microemulsions containing reducing agents and metal salts as bases for the synthesis of metallic nanoparticles.

    Science.gov (United States)

    Najjar, Reza; Stubenrauch, Cosima

    2009-03-01

    We studied the phase diagrams of microemulsions with a view to using these systems for the synthesis of metallic Pt, Pb, and Bi nanoparticles as well as of intermetallic Pt/Pb and Pt/Bi nanoparticles. The microemulsions consisted of H(2)O/salt-n-decane-SDS-1-butanol. The salt was either one metal precursor (H(2)PtCl(6) x 6 H(2)O, Pb(NO(3))(2), or Bi(NO(3))(3) x 5 H(2)O), a mixture of two metal precursors (H(2)PtCl(6) x 6 H(2)O + Pb(NO(3))(2) or H(2)PtCl(6) x 6 H(2)O + Bi(NO(3))(3) x 5 H(2)O), or the reducing agent (NaBH(4)). In addition, other salts needed to be added in order to solubilize the metal precursors, to stabilize the reducing agent, and to adjust the ionic strength. Combining the microemulsion (mu e1) that contains the metal precursor(s) with the microemulsion (mu e2) that contains the reducing agent leads to metallic nanoparticles. To study systematically how the shape and size of the synthesized metallic nanoparticles depend on the size and shape of the respective microemulsion droplets, first of all one has to find those conditions under which mu e1 and mu e2 have the same structure. For that purpose we determined the water emulsification failure boundary (wefb) of each microemulsion as it is at the wefb where the water droplets are known to be spherical. We found that the ionic strength (I) of the aqueous phase as well as the hard acid and hard base properties of the ions are the key tuning parameters for the location of the wefb.

  15. Comparison of Two Novel Solution-Based Routes for the Synthesis of Equiaxed ZnO Nanoparticles

    Directory of Open Access Journals (Sweden)

    K. Elen

    2011-01-01

    Full Text Available Due to a dominant one-dimensional growth rate, nanoparticles of zinc oxide often show a rodlike morphology. As a result, the synthesis of small spherical nanoparticles of undoped ZnO remains challenging. This paper presents two procedures that successfully produce a powder consisting of equiaxed zinc oxide nanoparticles: one using a polyethylene glycol- (PEG- assisted solvothermal method and the other by calcination of zinc oxalate obtained from a microemulsion-mediated method. In the latter, zinc-substituted aerosol OT (AOT is used as a surfactant. The samples are characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES, thermogravimetric analysis (TGA, X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, transmission electron microscopy (TEM, photon correlation spectroscopy (PCS, and photoluminescence (PL spectroscopy. Both synthesis techniques produce nanoparticles with similar sizes in the range of 10 to 20 nm. Dense aggregates observed in the calcined powder are infrequent in the case of the solvothermal method.

  16. Sonoelectrochemical Synthesis of Nanoparticles

    Directory of Open Access Journals (Sweden)

    Veronica Sáez

    2009-10-01

    Full Text Available This article reviews the nanomaterials that have been prepared to date by pulsed sonoelectrochemistry. The majority of nanomaterials produced by this method are pure metals such as silver, palladium, platinum, zinc, nickel and gold, but more recently the syntheses have been extended to include the preparation of nanosized metallic alloys and metal oxide semiconductors. A major advantage of this methodology is that the shape andsize of the nanoparticles can be adjusted by varying the operating parameters which include ultrasonic power, current density, deposition potential and the ultrasonic vs electrochemical pulse times. Together with these, it is also possible to adjust the pH, temperature and composition of the electrolyte in the sonoelectrochemistry cell.

  17. Synthesis and energy transfer within carbon-based fluorescent rare earth nanoparticles and nanocomposites (Conference Presentation)

    Science.gov (United States)

    Yust, Brian G.; Chipara, Mircea; Saenz, Aaron

    2016-03-01

    Recently, there has been a great deal of interest in fluorescent and upconverting rare earth-based nanoparticles for biomedical imaging and photodynamic therapy applications. While many of the widely explored upconverting contrast agents are comprised of fluoride or oxide crystal structures, very little work has been done to investigate the up- and downconversion emission in rare earth-doped carbon nanocomposites. Of particular interest, graphene-UCNP nanocomposites and sesquicarbide nanoparticles may offer a wide range of new applications when coupled with the extraordinary optical properties of rare earth-doped systems, such as potential use as nano-transducers. Carbon-based nanocomposites and sesquicarbides doped with rare earth elements were synthesized using the microwave and solvothermal methods with additional brief high temperature heat treatments. They were then characterized by XRD, visible and NIR excitation and emission spectroscopy, as well as Raman spectrsocopy. Tuning of the emission manifold ratios was explored through different compositions and size. Also, energy transfer between the emitting ions and the electronic states of the host structure was explored. Finally, cytotoxicity was tested, and cellular uptake of these nanomaterials was performed with confocal microscopy.

  18. Nanocomposites Based on Technical Polymers and Sterically Functionalized Soft Magnetic Magnetite Nanoparticles: Synthesis, Processing, and Characterization

    Directory of Open Access Journals (Sweden)

    S. Kirchberg

    2012-01-01

    The distribution of the nanoparticles is characterized by microscopy. Besides a minor number of agglomerates and aggregates the nanoparticles are distributed homogeneously in the PVB composites. Furthermore, the injection molded specimens are characterized with regard to their thermal degradation, polymer structure, and their mechanical and magnetic properties. The presence of nanoparticles capped with ricinoleic acid shows significant decrease in degradation temperature and in glass transition temperature of PVB. The degradation temperature of PMMA is increased by adding nanoparticles capped with oleic acid. Dynamic-mechanical properties as well as the magnetic permeability of PVB and PMMA are improved significantly by adding nanoparticles.

  19. SYNTHESIS OF COPPER NANOPARTICLES BY ASPERGILLUS SPECIES

    OpenAIRE

    Kantabathini Venkata Pavani; Nandigam Srujana; Guntur Preethi; Tandale Swati

    2013-01-01

    Recent developments in the biosynthesis of nanomaterials have demonstrated the important role of microorganisms in nanotechnology. The organisms show a unique potential in environmentally friendly production and accumulation of nanoparticles with different shapes and sizes. The present study proposed a green process for synthesis of copper nanoparticles using Aspergillus species. Syntheses of copper nanoparticles were characterized by UV-visible spectroscopy. The extracellular synthesis of co...

  20. Synthesis of iron-based nanoparticles using oolong tea extract for the degradation of malachite green

    Science.gov (United States)

    Huang, Lanlan; Weng, Xiulan; Chen, Zuliang; Megharaj, Mallavarapu; Naidu, Ravendra

    2014-01-01

    Iron-based nanoparticles (OT-FeNP) were synthesized using oolong tea extracts. Their morphology, structure and size were confirmed by scanning electron microscopy (SEM), X-ray energy-dispersive spectroscopy (EDS), X-ray diffraction (XRD), UV-visible (UV-vis) and Fourier Transform Infrared spectroscopy (FTIR). Formation of FeNP results in mostly spherical particles with diameters ranging from 40 to 50 nm. Degradation of malachite green (MG) using OT-FeNP demonstrated that kinetics fitted well to the pseudo first-order reaction by removing 75.5% of MG (50 mg/L). This indicated that OT-FeNP has the potential to serve as a green nanomaterial for environmental remediation.

  1. Conductive photopolymers : Insitu synthesis of metal nanoparticles

    OpenAIRE

    Nazar, Rabia

    2015-01-01

    A prologue to the field of noble metal nanoparticles is presented with a brief commentary on the basic synthesis techniques to manufacture these metal nanoparticles and to exploit the full use of their unique properties. In recent years scientific interest in embedding the metal nanoparticles in a host polymer has been increased significantly. A great advancement in the field of conductive polymers by embedding metal nanoparticles in them has been witnessed because they are likely to be an al...

  2. Dealloying-based facile synthesis and highly catalytic properties of Au core/porous shell nanoparticles

    Science.gov (United States)

    Kim, Minho; Ko, Sung Min; Nam, Jwa-Min

    2016-06-01

    Porous nanostructures exhibit excellent catalytic properties due to high surface-to-volume ratio, good surface reactivity and various structural features, but controlling the distribution, size, shape and density of pores and structural features of these particles is highly challenging. Herein, we report a tunable dealloying-based facile synthetic strategy to form highly porous Au core/porous shell nanoparticles (CPS NPs) in high yield by selectively dissolving Ag atoms from Au/Au-Ag core/alloy shell NPs. The CPS NPs exhibit a very short induction time, high conversion rate constant, low activation energy and high turnover frequency due to their catalytically active porous shells containing networked thin ligaments, surface defects, ultra-high porosity and photothermal properties. The CPS NPs are more catalytic Au NPs than other reported Au nanostructures, and the strategy and results open avenues in porous nanostructures and nanocatalysts.Porous nanostructures exhibit excellent catalytic properties due to high surface-to-volume ratio, good surface reactivity and various structural features, but controlling the distribution, size, shape and density of pores and structural features of these particles is highly challenging. Herein, we report a tunable dealloying-based facile synthetic strategy to form highly porous Au core/porous shell nanoparticles (CPS NPs) in high yield by selectively dissolving Ag atoms from Au/Au-Ag core/alloy shell NPs. The CPS NPs exhibit a very short induction time, high conversion rate constant, low activation energy and high turnover frequency due to their catalytically active porous shells containing networked thin ligaments, surface defects, ultra-high porosity and photothermal properties. The CPS NPs are more catalytic Au NPs than other reported Au nanostructures, and the strategy and results open avenues in porous nanostructures and nanocatalysts. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr01321j

  3. Synthesis and Bioconjugation of Gold Nanoparticles as Potential Molecular Probes for Light-Based Imaging Techniques

    NARCIS (Netherlands)

    Rayavarapu, Raja Gopal; Petersen, Wilma; Ungureanu, Constantin; Post, Janine N.; Leeuwen, van Ton G.; Manohar, Srirang

    2007-01-01

    We have synthesized and characterized gold nanoparticles (spheres and rods) with optical extinction bands within the “optical imaging window.” The intense plasmon resonant driven absorption and scattering peaks of these nanoparticles make them suitable as contrast agents for optical imaging techniqu

  4. Electrochemical synthesis of a graphene sheet and gold nanoparticle-based nanocomposite, and its application to amperometric sensing of dopamine

    International Nuclear Information System (INIS)

    We describe a simple, green and controllable approach for electrochemical synthesis of a nanocomposite made up from electrochemically reduced graphene oxide (ERGO) and gold nanoparticles. This material possesses the specific features of both gold nanoparticles and graphene. Its morphology was characterized by scanning electron microscopy which reveals a homogeneous distribution of gold nanoparticles on the graphene sheets. Cyclic voltammetry was used to evaluate the electrochemical properties of this nanocomposite towards dopamine by modification of it on surface of glassy carbon electrode (GCE). Compared to the bare GCE, the electrode modified with gold nanoparticles, and the electrode modified with ERGO, the one modified with the nanocomposite displays better electrocatalytic activity. Its oxidation peak current is linearly proportional to the concentration of dopamine (DA) in the range from 0. 1 to 10 μM, with a detection limit of 0. 04 μM (at S/N = 3). The modified electrode also displays good storage stability, reproducibility, and selectivity. (author)

  5. Colloidosome-based synthesis of a multifunctional nanostructure of silver and hollow iron oxide nanoparticles

    KAUST Repository

    Pan, Yue

    2010-03-16

    Nanoparticles that self-assemble on a liquid-liquid interface serve as the building block for making heterodimeric nanostructures. Specifically, hollow iron oxide nanoparticles within hexane form colloidosomes in the aqueous solution of silver nitrate, and iron oxide exposed to the aqueous phase catalyzes the reduction of silver ions to afford a heterodimer of silver and hollow iron oxide nanoparticles. Transmission electron microscopy, selected area electron diffraction, energy-dispersive X-ray spectrometry, X-ray diffraction, UV-vis spectroscopy, and SQUID were used to characterize the heterodimers. Interestingly, the formation of silver nanoparticles helps the removal of spinglass layer on the hollow iron oxide nanoparticles. This work demonstrates a powerful yet convenient strategy for producing sophisticated, multifunctional nanostructures. © 2010 American Chemical Society.

  6. Phase transfer synthesis of N,N'(1,2-phenylene)bis-hippuricamide tethered metal based functionalized nanoparticles: A study on some novel microbial targeting peptide-mimic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Raman, N., E-mail: drn_raman@yahoo.co.in [Research Department of Chemistry, VHNSN College, Virudhunagar 626 001 (India); Sudharsan, S. [Research Department of Chemistry, VHNSN College, Virudhunagar 626 001 (India)

    2011-10-01

    This paper presents the novel synthesis of peptide, N,N'(1,2-phenylene)bis-hippuricamide tethered metal [Cu(II), Zn(II), Ni(II) and Co(II)] based functionalized nanoparticles via modified Brust-Schiffrin methodology. The growth, organic composition and morphology of these functionalized nanoparticles have been evaluated by UV-Vis, FT-IR spectroscopy and scanning electron microscopy. They are structurally and thermally characterized by X-ray diffraction and thermogravimetric analysis. Moreover, the interfacial dealings of these functionalized nanoparticles with Calf-thymus DNA and pUC19 DNA reveal that the functionalized nanoparticles of cobalt is an effective DNA damaging agent under physiological conditions. This has been supported by its efficient antimicrobial character against few fungal and bacterial strains, thereby steering its way towards biomedical applications as a metal based nanocarrier.

  7. Microwave assisted template synthesis of silver nanoparticles

    Indian Academy of Sciences (India)

    K J Sreeram; M Nidhin; B U Nair

    2008-12-01

    Easier, less time consuming, green processes, which yield silver nanoparticles of uniform size, shape and morphology are of interest. Various methods for synthesis, such as conventional temperature assisted process, controlled reaction at elevated temperatures, and microwave assisted process have been evaluated for the kind of silver nanoparticles synthesized. Starch has been employed as a template and reducing agent. Electron microscopy, photon correlation spectroscopy and surface plasmon resonance have been employed to characterize the silver nanoparticles synthesized. Compared to conventional methods, microwave assisted synthesis was faster and provided particles with an average particle size of 12 nm. Further, the starch functions as template, preventing the aggregation of silver nanoparticles.

  8. Optical nanoparticles: synthesis and biomedical application

    Science.gov (United States)

    Nhung Tran, Hong; Nghiem, Thi Ha Lien; Thuy Duong Vu, Thi; Chu, Viet Ha; Huan Le, Quang; Nhung Hoang, Thi My; Thanh Nguyen, Lai; Pham, Duc Minh; Thuan Tong, Kim; Hoa Do, Quang; Vu, Duong; Nghia Nguyen, Trong; Tan Pham, Minh; Nguyen Duong, Cao; Thuy Tran, Thanh; Son Vu, Van; Thuy Nguyen, Thi; Nguyen, Thi Bich Ngoc; Tran, Anh Duc; Thuong Trinh, Thi; Nguyen, Thi Thai An

    2015-01-01

    This paper presents a summary of our results on studies of synthesis and biomedical application of optical nanoparticles. Gold, dye-doped silica based and core-shell multifunctional multilayer (SiO2/Au, Fe3O4/SiO2, Fe3O4/SiO2/Au) water-monodispersed nanoparticles were synthesized by chemical route and surface modified with proteins and biocompatible chemical reagents. The particles were conjugated with antibody or aptamer for specific detecting and imaging bacteria and cancer cells. The photothermal effects of gold nanoshells (SiO2/Au and Fe3O4/SiO2/Au) on cells and tissues were investigated. The nano silver substrates were developed for surface enhanced Raman scattering (SERS) spectroscopy to detect melamine.

  9. Facile chemical synthesis and structure characterization of copper molybdate nanoparticles

    Science.gov (United States)

    Rahimi-Nasrabadi, Mehdi; Pourmortazavi, Seied Mahdi; Khalilian-Shalamzari, Morteza

    2015-03-01

    Experimental parameters of a synthesis route were optimized by Taguchi robust design for the facile and controllable synthesis of copper molybdate nanoparticles. CuMoO4 nanoparticles were synthesized by chemical precipitation followed by hydrothermal process. Effects of different parameters of synthesis procedure, i.e. concentrations of both reagents, copper feeding flow rate and temperature of reactor on the particle size of prepared copper molybdate nanoparticles were investigated. The results of statistical optimization revealed that the size of copper molybdate particles is dependent on the procedure variables involving copper concentrations, flow rate and temperature of the reactor; while, molybdate concentration has a no considerable role in determining the size of CuMoO4 particles. Based on the results obtained by statistical optimization process, the nanoparticles of copper molybdate were prepared and then their structure and chemical composition were characterized by various techniques, i.e. SEM, TEM, XRD, EDX, FT-IR, UV-Vis and photoluminescence spectroscopy.

  10. Green synthesis of silver nanoparticles using tannins

    Science.gov (United States)

    Raja, Pandian Bothi; Rahim, Afidah Abdul; Qureshi, Ahmad Kaleem; Awang, Khalijah

    2014-09-01

    Colloidal silver nanoparticles were prepared by rapid green synthesis using different tannin sources as reducing agent viz. chestnut (CN), mangrove (MG) and quebracho (QB). The aqueous silver ions when exposed to CN, MG and QB tannins were reduced which resulted in formation of silver nanoparticles. The resultant silver nanoparticles were characterized using UV-Visible, X-ray diffraction (XRD), scanning electron microscopy (SEM/EDX), and transmission electron microscopy (TEM) techniques. Furthermore, the possible mechanism of nanoparticles synthesis was also derived using FT-IR analysis. Spectroscopy analysis revealed that the synthesized nanoparticles were within 30 to 75 nm in size, while XRD results showed that nanoparticles formed were crystalline with face centered cubic geometry.

  11. Bioinspired synthesis of magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    David, Anand

    2009-05-26

    The synthesis of magnetic nanoparticles has long been an area of active research. Magnetic nanoparticles can be used in a wide variety of applications such as magnetic inks, magnetic memory devices, drug delivery, magnetic resonance imaging (MRI) contrast agents, and pathogen detection in foods. In applications such as MRI, particle uniformity is particularly crucial, as is the magnetic response of the particles. Uniform magnetic particles with good magnetic properties are therefore required. One particularly effective technique for synthesizing nanoparticles involves biomineralization, which is a naturally occurring process that can produce highly complex nanostructures. Also, the technique involves mild conditions (ambient temperature and close to neutral pH) that make this approach suitable for a wide variety of materials. The term 'bioinspired' is important because biomineralization research is inspired by the naturally occurring process, which occurs in certain microorganisms called 'magnetotactic bacteria'. Magnetotactic bacteria use biomineralization proteins to produce magnetite crystals having very good uniformity in size and morphology. The bacteria use these magnetic particles to navigate according to external magnetic fields. Because these bacteria synthesize high quality crystals, research has focused on imitating aspects of this biomineralization in vitro. In particular, a biomineralization iron-binding protein found in a certain species of magnetotactic bacteria, magnetospirillum magneticum, AMB-1, has been extracted and used for in vitro magnetite synthesis; Pluronic F127 gel was used to increase the viscosity of the reaction medium to better mimic the conditions in the bacteria. It was shown that the biomineralization protein mms6 was able to facilitate uniform magnetite synthesis. In addition, a similar biomineralization process using mms6 and a shorter version of this protein, C25, has been used to synthesize cobalt ferrite

  12. Bioinspired synthesis of magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    David, Anand [Iowa State Univ., Ames, IA (United States)

    2009-01-01

    The synthesis of magnetic nanoparticles has long been an area of active research. Magnetic nanoparticles can be used in a wide variety of applications such as magnetic inks, magnetic memory devices, drug delivery, magnetic resonance imaging (MRI) contrast agents, and pathogen detection in foods. In applications such as MRI, particle uniformity is particularly crucial, as is the magnetic response of the particles. Uniform magnetic particles with good magnetic properties are therefore required. One particularly effective technique for synthesizing nanoparticles involves biomineralization, which is a naturally occurring process that can produce highly complex nanostructures. Also, the technique involves mild conditions (ambient temperature and close to neutral pH) that make this approach suitable for a wide variety of materials. The term 'bioinspired' is important because biomineralization research is inspired by the naturally occurring process, which occurs in certain microorganisms called 'magnetotactic bacteria'. Magnetotactic bacteria use biomineralization proteins to produce magnetite crystals having very good uniformity in size and morphology. The bacteria use these magnetic particles to navigate according to external magnetic fields. Because these bacteria synthesize high quality crystals, research has focused on imitating aspects of this biomineralization in vitro. In particular, a biomineralization iron-binding protein found in a certain species of magnetotactic bacteria, magnetospirillum magneticum, AMB-1, has been extracted and used for in vitro magnetite synthesis; Pluronic F127 gel was used to increase the viscosity of the reaction medium to better mimic the conditions in the bacteria. It was shown that the biomineralization protein mms6 was able to facilitate uniform magnetite synthesis. In addition, a similar biomineralization process using mms6 and a shorter version of this protein, C25, has been used to synthesize cobalt ferrite

  13. Fabrication of PDMS-Based Microfluidic Devices: Application for Synthesis of Magnetic Nanoparticles

    Science.gov (United States)

    Thu, Vu Thi; Mai, An Ngoc; Le The Tam; Van Trung, Hoang; Thu, Phung Thi; Tien, Bui Quang; Thuat, Nguyen Tran; Lam, Tran Dai

    2016-05-01

    In this work, we have developed a convenient approach to synthesize magnetic nanoparticles with relatively high magnetization and controllable sizes. This was realized by combining the traditional co-precipitation method and microfluidic techniques inside microfluidic devices. The device was first designed, and then fabricated using simplified soft-lithography techniques. The device was utilized to synthesize magnetite nanoparticles. The synthesized nanomaterials were thoroughly characterized using field emission scanning electron microscopy and a vibrating sample magnetometer. The results demonstrated that the as-prepared device can be utilized as a simple and effective tool to synthesize magnetic nanoparticles with the sizes less than 10 nm and magnetization more than 50 emu/g. The development of these devices opens new strategies to synthesize nanomaterials with more precise dimensions at narrow size-distribution and with controllable behaviors.

  14. Synthesis and Characterization of Gold Nanoparticles

    OpenAIRE

    Hedkvist, Olof

    2013-01-01

    This thesis is focused on the synthesis of three different shapes of gold nanoparticles; the gold nanosphere, the gold nanorod and the gold nanocube. These will be synthesized using wet chemistry methods and characterized using UV-Vis- NIR spectroscopy and dynamic light scattering. The results will be used to draw some conclusions as to what factors influence the growth of gold nanoparticles.

  15. A green chemistry-based classification model for the synthesis of silver nanoparticles

    Science.gov (United States)

    The assessment of implementation of green chemistry principles in the synthesis of nanomaterials is a complex decision-making problem that necessitates integration of several evaluation criteria. Multiple Criteria Decision Aiding (MCDA) provides support for such a challenge. One ...

  16. A Facile pH Controlled Citrate-Based Reduction Method for Gold Nanoparticle Synthesis at Room Temperature.

    Science.gov (United States)

    Tyagi, Himanshu; Kushwaha, Ajay; Kumar, Anshuman; Aslam, Mohammed

    2016-12-01

    The synthesis of gold nanoparticles using citrate reduction process has been revisited. A simplified room temperature approach to standard Turkevich synthesis is employed to obtain fairly monodisperse gold nanoparticles. The role of initial pH alongside the concentration ratio of reactants is explored for the size control of Au nanoparticles. The particle size distribution has been investigated using UV-vis spectroscopy and transmission electron microscope (TEM). At optimal pH of 5, gold nanoparticles obtained are highly monodisperse and spherical in shape and have narrower size distribution (sharp surface plasmon at 520 nm). For other pH conditions, particles are non-uniform and polydisperse, showing a red-shift in plasmon peak due to aggregation and large particle size distribution. The room temperature approach results in highly stable "colloidal" suspension of gold nanoparticles. The stability test through absorption spectroscopy indicates no sign of aggregation for a month. The rate of reduction of auric ionic species by citrate ions is determined via UV absorbance studies. The size of nanoparticles under various conditions is thus predicted using a theoretical model that incorporates nucleation, growth, and aggregation processes. The faster rate of reduction yields better size distribution for optimized pH and reactant concentrations. The model involves solving population balance equation for continuously evolving particle size distribution by discretization techniques. The particle sizes estimated from the simulations (13 to 25 nm) are close to the experimental ones (10 to 32 nm) and corroborate the similarity of reaction processes at 300 and 373 K (classical Turkevich reaction). Thus, substitution of experimentally measured rate of disappearance of auric ionic species into theoretical model enables us to capture the unusual experimental observations. PMID:27526178

  17. A Facile pH Controlled Citrate-Based Reduction Method for Gold Nanoparticle Synthesis at Room Temperature

    Science.gov (United States)

    Tyagi, Himanshu; Kushwaha, Ajay; Kumar, Anshuman; Aslam, Mohammed

    2016-08-01

    The synthesis of gold nanoparticles using citrate reduction process has been revisited. A simplified room temperature approach to standard Turkevich synthesis is employed to obtain fairly monodisperse gold nanoparticles. The role of initial pH alongside the concentration ratio of reactants is explored for the size control of Au nanoparticles. The particle size distribution has been investigated using UV-vis spectroscopy and transmission electron microscope (TEM). At optimal pH of 5, gold nanoparticles obtained are highly monodisperse and spherical in shape and have narrower size distribution (sharp surface plasmon at 520 nm). For other pH conditions, particles are non-uniform and polydisperse, showing a red-shift in plasmon peak due to aggregation and large particle size distribution. The room temperature approach results in highly stable "colloidal" suspension of gold nanoparticles. The stability test through absorption spectroscopy indicates no sign of aggregation for a month. The rate of reduction of auric ionic species by citrate ions is determined via UV absorbance studies. The size of nanoparticles under various conditions is thus predicted using a theoretical model that incorporates nucleation, growth, and aggregation processes. The faster rate of reduction yields better size distribution for optimized pH and reactant concentrations. The model involves solving population balance equation for continuously evolving particle size distribution by discretization techniques. The particle sizes estimated from the simulations (13 to 25 nm) are close to the experimental ones (10 to 32 nm) and corroborate the similarity of reaction processes at 300 and 373 K (classical Turkevich reaction). Thus, substitution of experimentally measured rate of disappearance of auric ionic species into theoretical model enables us to capture the unusual experimental observations.

  18. Synthesis and characterization of CdS nanoparticle based multiwall carbon nanotube-maleic anhydride-1-octene nanocomposites

    Science.gov (United States)

    Malikov, E. Y.; Altay, M. C.; Muradov, M. B.; Akperov, O. H.; Eyvazova, G. M.; Puskás, R.; Madarász, D.; Kukovecz, Á.; Kónya, Z.

    2015-05-01

    CdS nanoparticles were synthesized by sonication from cadmium chloride and thiourea using a multiwall carbon nanotube (MWCNT)-maleic anhydride (MA)-1-octene system as the matrix. The matrix was obtained by the "grafting from" approach from oxidized carbon nanotubes and maleic anhydride-1-octene. Multiwall carbon nanotubes used for reinforcing the matrix were synthesized by Catalytic Chemical Vapor Deposition using Fe-Co/Al2O3 as the catalyst. The obtained nanostructures were characterized by FTIR, XRD, Raman spectroscopy, TEM, SEM and UV-vis spectroscopy. The average CdS particle diameter was 7.9 nm as confirmed independently by TEM and XRD. UV-vis spectroscopy revealed that the obtained nanostructure is an appropriate base material for making optical devices. The novelty of this work is the use of the MWCNT-MA-1-octene matrix obtained via the "grafting from" approach for the synthesis of uniformly dispersed CdS nanocrystals by ultrasonic cavitation to obtain a polymer nanocomposite.

  19. Colloidal-chemistry based synthesis of quantized CuInS2/Se2 nanoparticles

    Directory of Open Access Journals (Sweden)

    Abazović Nadica D.

    2012-01-01

    Full Text Available Ternary chalcogenide nanoparticles, CuInS2 and CuInSe2, were synthesized in high- temperature boiling organic non-polar solvent. The X-ray diffraction analysis revealed that both materials have tetragonal (chalcopyrite crystal structure. Morphology of the obtained materials was revealed by using transmission electron microscopy. Agglomerated spherical CuInS2 nanoparticles with broad size distribution in the range from 2 to 20 nm were obtained. In the case of CuInSe2, isolated particles with spherical or prismatic shape in the size range from 10 to 25 nm were obtained, as well as agglomerates consisting of much smaller particles with diameter of about 2-5 nm. The particles with the smallest diameters of both materials exhibit quantum size effect.

  20. Green synthesis and characterization of gelatin-based and sugar-reduced silver nanoparticles

    OpenAIRE

    Majid Darroudi; Mansor Bin Ahmad; Abdul Halim Abdullah; et al

    2011-01-01

    Majid Darroudi1,2, Mansor Bin Ahmad3, Abdul Halim Abdullah1,3, Nor Azowa Ibrahim31Advanced Materials and Nanotechnology Laboratory, Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Selangor, Malaysia; 2Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran; 3Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, Selangor, MalaysiaAbstract: Silver nanoparticles (Ag-NPs) have been successfully prepared with simple and &...

  1. Sonochemical Synthesis of Cobalt Ferrite Nanoparticles

    Directory of Open Access Journals (Sweden)

    Partha P. Goswami

    2013-01-01

    Full Text Available Cobalt ferrite being a hard magnetic material with high coercivity and moderate magnetization has found wide-spread applications. In this paper, we have reported the sonochemical synthesis of cobalt ferrite nanoparticles using metal acetate precursors. The ferrite synthesis occurs in three steps (hydrolysis of acetates, oxidation of hydroxides, and in situ microcalcination of metal oxides that are facilitated by physical and chemical effects of cavitation bubbles. The physical and magnetic properties of the ferrite nano-particles thus synthesized have been found to be comparable with those reported in the literature using other synthesis techniques.

  2. Synthesis of Quercetin Loaded Nanoparticles Based on Alginate for Pb(II) Adsorption in Aqueous Solution

    Science.gov (United States)

    Qi, Yun; Jiang, Meng; Cui, Yuan-Lu; Zhao, Lin; Zhou, Xia

    2015-10-01

    Pb(II) is a representative heavy metal in industrial wastewater, which may frequently cause serious hazard to living organisms. In this study, comparative studies between alginate nanoparticles (AN) and quercetin-decorated alginate nanoparticles (Q-AN) were investigated for Pb(II) ion adsorption. Characterization of AN and Q-AN were analysed by transmission electron microscopy (TEM), Fourier transform infrared spectrometry (FT-IR), X-ray diffractometer (XRD), and thermogravimetric analysis (TG-DTG-DSC). The main operating conditions such as pH, initial concentration of Pb(II), and co-existing metal ions were also investigated using a batch experiment. AN and Q-AN, with a diameter of 95.06 and 58.23 nm, were constituted by many small primary nanoparticles. It revealed that when initial concentration of Pb(II) is between 250 and 1250 mg L-1, the adsorption rate and equilibrium adsorption were increased with the increase of pH from 2 to 7. The maximum adsorption capacities of 147.02 and 140.37 mg L-1 were achieved by AN and Q-AN, respectively, with 0.2 g adsorbents in 1000 mg L-1 Pb(II) at pH 7. The adsorption rate of Pb(II) was little influenced by the co-existing metal ions, such as Mn(II), Co(II), and Cd(II). Desorption experiments showed that Q-AN possessed a higher desorption rate than AN, which were 90.07 and 83.26 %, respectively. AN and Q-AN would probably be applied as adsorbents to remove Pb(II) and then recover it from wastewater for the advantages of simple preparation, high adsorption capacity, and recyclability.

  3. Synthesis of environmentally friendly highly dispersed magnetite nanoparticles based on rosin cationic surfactants as thin film coatings of steel.

    Science.gov (United States)

    Atta, Ayman M; El-Mahdy, Gamal A; Al-Lohedan, Hamad A; Al-Hussain, Sami A

    2014-04-22

    This work presents a new method to prepare monodisperse magnetite nanoparticles capping with new cationic surfactants based on rosin. Core/shell type magnetite nanoparticles were synthesized using bis-N-(3-levopimaric maleic acid adduct-2-hydroxy) propyl-triethyl ammonium chloride (LPMQA) as capping agent. Fourier transform infrared spectroscopy (FTIR) was employed to characterize the nanoparticles chemical structure. Transmittance electron microscopies (TEM) and X-ray powder diffraction (XRD) were used to examine the morphology of the modified magnetite nanoparticles. The magnetite dispersed aqueous acid solution was evaluated as an effective anticorrosion behavior of a hydrophobic surface on steel. The inhibition effect of magnetite nanoparticles on steel corrosion in 1 M HCl solution was investigated using potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS). Results obtained from both potentiodynamic polarisation and EIS measurements reveal that the magnetite nanoparticle is an effective inhibitor for the corrosion of steel in 1.0 M HCl solution. Polarization data show that magnetite nanoparticles behave as a mixed type inhibitor. The inhibition efficiencies obtained from potentiodynamic polarization and EIS methods are in good agreement.

  4. Synthesis of Environmentally Friendly Highly Dispersed Magnetite Nanoparticles Based on Rosin Cationic Surfactants as Thin Film Coatings of Steel

    Directory of Open Access Journals (Sweden)

    Ayman M. Atta

    2014-04-01

    Full Text Available This work presents a new method to prepare monodisperse magnetite nanoparticles capping with new cationic surfactants based on rosin. Core/shell type magnetite nanoparticles were synthesized using bis-N-(3-levopimaric maleic acid adduct-2-hydroxy propyl-triethyl ammonium chloride (LPMQA as capping agent. Fourier transform infrared spectroscopy (FTIR was employed to characterize the nanoparticles chemical structure. Transmittance electron microscopies (TEM and X-ray powder diffraction (XRD were used to examine the morphology of the modified magnetite nanoparticles. The magnetite dispersed aqueous acid solution was evaluated as an effective anticorrosion behavior of a hydrophobic surface on steel. The inhibition effect of magnetite nanoparticles on steel corrosion in 1 M HCl solution was investigated using potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS. Results obtained from both potentiodynamic polarisation and EIS measurements reveal that the magnetite nanoparticle is an effective inhibitor for the corrosion of steel in 1.0 M HCl solution. Polarization data show that magnetite nanoparticles behave as a mixed type inhibitor. The inhibition efficiencies obtained from potentiodynamic polarization and EIS methods are in good agreement.

  5. Synthesis of gold nanoparticles and silver nanoparticles via green technology

    Science.gov (United States)

    Ahmed, Zulfiqaar; Balu, S. S.

    2012-11-01

    The proposed work describes the comparison of various methods of green synthesis for preparation of Gold and Silver nanoparticles. Pure extracts of Lemon (Citrus limon) and Tomato (Solanum lycopersicum) were mixed with aqueous solution of auric tetrachloride and silver nitrate. The resultant solutions were treated with four common techniques to assist in the reduction namely photo catalytic, thermal, microwave assisted reduction and solvo - thermal reduction. UV - Visible Spectroscopy results and STM images of the final solutions confirmed the formation of stable metallic nanoparticles. A preliminary account of the green synthesis work is presented here.

  6. The Synthesis of Anatase Nanoparticles and the Preparation of Photocatalytically Active Coatings Based on Wet Chemical Methods for Self-Cleaning Applications

    Directory of Open Access Journals (Sweden)

    Dejan Verhovšek

    2012-01-01

    Full Text Available We report on an improved sol-gel method for the production of highly photocatalytic titanium dioxide (TiO2 anatase nanoparticles which can provide appropriate control over the final characteristics of the nanoparticles, such as particle size, crystallinity, crystal structure, morphology, and also the degree of agglomeration. The synthesized anatase nanoparticles were characterized using various techniques, such as X-ray powder diffraction (XRD, scanning electron microscopy (SEM, and transmission electron microscopy (TEM, and were tested in coatings for self-cleaning glass and ceramic surfaces. The coatings were prepared using a soft chemistry route and are completely transparent to visible light and exhibit a high photocatalytic effect, which was determined by contact-angle measurements. Finally, it is worth mentioning that both the sol-gel synthesis method and the coating-preparation method are based on a wet chemical process, thus presenting no risk of handling the TiO2 anatase nanoparticles in their potentially hazardous powder form at any stage of our development. Low-price, easy-to-handle, and nontoxic materials were used. Therefore, our work represents an important contribution to the development of TiO2 anatase nanoparticle coatings that provide a high photocatalytic effect and can thus be used for numerous applications.

  7. Polymer/Iron Oxide Nanoparticle Composites—A Straight Forward and Scalable Synthesis Approach

    OpenAIRE

    Jens Sommertune; Abhilash Sugunan; Anwar Ahniyaz; Rebecca Stjernberg Bejhed; Anna Sarwe; Christer Johansson; Christoph Balceris; Frank Ludwig; Oliver Posth; Andrea Fornara

    2015-01-01

    Magnetic nanoparticle systems can be divided into single-core nanoparticles (with only one magnetic core per particle) and magnetic multi-core nanoparticles (with several magnetic cores per particle). Here, we report multi-core nanoparticle synthesis based on a controlled precipitation process within a well-defined oil in water emulsion to trap the superparamagnetic iron oxide nanoparticles (SPION) in a range of polymer matrices of choice, such as poly(styrene), poly(lactid acid), poly(methyl...

  8. Green Synthesis of Gold Nanoparticles

    OpenAIRE

    Hamid Reza Ghorbani

    2015-01-01

    There is an increased interest in understanding the toxicity and rational design of gold nanoparticles for biomedical applications in recent years. In this study gold nanoparticles were synthesized using dextrose as a reducing agent. The gold nanoparticles displayed characteristic Surface Plasmon Resonance peak at around 550 nm having a mean particle size of 75±30 nm. In order to identify and analyze nanoparticles, UV–Vis spectroscopy, Scanning electron microscopy (SEM), and dynamic light sca...

  9. The synthesis and characterization of iron nanoparticles

    Science.gov (United States)

    Bennett, Tyler

    Nanoparticle synthesis has garnered attention for technological applications for catalysts, industrial processing, and medical applications. The size ranges for these is in the particles nanostructural domain. Pure iron nanoparticles have been of particular interest for their reactivity and relative biological inertness. Applications include cancer treatment and carrying medicine to a relevant site. Unfortunately, because of their reactivity, pure iron nanoparticles have been difficult to study. This is because of their accelerated tendency to form oxides in air, due to the increased surface area to volume ratio. Using synthesis processes with polyphenols or long chain amines, air stable iron nanoparticles have been produced with a diameter size range of ~ 2 to about ~10 nm, but apparently have transformed due to internal pressure and crystallographic defects to the FCC phase. The FCC crystals have been seen to form icosahedral and decahedral shapes. This size is within the range for use as a catalyst for the growth of both carbon nanotubes and boron nitride nanotubes as well for biomedical applications. The advantages of these kinds of catalysts are that nanotube growth can be for the first time separated from the catalyst formation. Additionally, the catalyst size can be preselected for a certain size nanotube to grow. In summary: (1) we found the size distributions of nanoparticles for various synthesis processes, (2) we discovered the right size range for growth of nanotubes from the iron nanoparticles, (3) the nanoparticles are under a very high internal pressure, (4) the nanoparticles are in the FCC phase, (5) they appear to be in icosahedral and decahedral structures, (6) they undergo room temperature twinning, (7) the FCC crystals are distorted due to carbon in octahedral sites, (8) the iron nanoparticles are stable in air, (9) adding small amounts of copper make the iron nanoparticles smaller.

  10. Microfluidic Reactors for the Controlled Synthesis of Nanoparticles

    Science.gov (United States)

    Erdem, Emine Yegan

    temperature nanoparticle synthesis. This microreactor was fabricated by using a CO 2-laser printer, which is an inexpensive method for fabricating microfluidic devices and it is a relatively fast way compared to other fabrication techniques. Iron oxide nanoparticle synthesis was demonstrated using this reactor and size distributions with a standard deviation of 10% was obtained. The second microreactor presented in this work was designed to produce monodisperse nanoparticles by utilizing thermally isolated heated and cooled regions for separating nucleation and growth processes. This microreactor was made out of silicon and it was used to demonstrate the synthesis of TiO 2 nanoparticles. Size distributions with less than 10% standard deviation were achieved. This microreactor also provides a platform for studying the effects of temperature and residence times which is very important to understand the reaction kinetics of nanoparticle synthesis. In this work, two microfluidic techniques for retrieving nanoparticles from the microreactors were also discussed. The first method was based on trapping the aqueous droplet phase inside the microchannel and the second method was utilizing a micropost array to direct droplets from the oil solution to the pure water. As a final step, a printing technique was used to print nanoparticles synthesized inside the microreactors for future applications. This ability is important for achieving smart surfaces that can utilize the properties of nanoparticles for sensing applications in the future.

  11. Plasma Catalytic Synthesis of Silver Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yu-Tao; GUO Ying; MA Teng-Cai

    2011-01-01

    We present the experimental results of plasma catalytic synthesis of colloidal silver nanoparticles, using AgNO3 as the precursor, ethanol as the solvent and reducing agent, and poly vinyl pyrrolidone (PVP) as the macromolecular surfactant. The plasma is generated by an atmospheric argon dielectric barrier discharge jet. Silver nanoparticles are produced instantly once the plasma is ignited. The system is not heated so it is necessary to use traditional chemical methods. The samples are characterized by UV-visible absorbance and transmission electron microscopy. For glow discharge mode no obvious silver nanoparticles are observed. For low voltage filamentary streamer discharge mode a lot of silver nanoparticles with the mean diameter of ~3.5nm are generated and a further increase of the voltage causes the occurrence of agglomeration.%We present the experimental results of plasma catalytic synthesis of colloidal silver nanoparticles,using AgNO3 as the precursor,ethanol as the solvent and reducing agent,and poly vinyl pyrrolidone (PVP) as the macromolecular surfactant.The plasma is generated by an atmospheric argon dielectric barrier discharge jet.Silver nanoparticles are produced instantly once the plasma is ignited.The system is not heated so it is necessary to use traditional chemical methods.The samples are characterized by UV-visible absorbance and transmission electron microscopy.For glow discharge mode no obvious silver nanoparticles are observed.For low voltage filamentary streamer discharge mode a lot of silver nanoparticles with the mean diameter of ~3.5nm are generated and a further increase of the voltage causes the occurrence of agglomeration.The study of silver nanoparticles has been an extremely active area in recent years because of their important physical and chemical properties as a catalyst and antimicrobial reagent,for example.A number of methods for silver nanoparticle preparation have been developed,[1-3] among them chemical reduction is

  12. Metal Oxide Nanoparticles for Contrast Enhancement in Magnetic Resonance Imaging : Synthesis, Functionalization and Characterization

    OpenAIRE

    Ahrén, Maria

    2013-01-01

    This thesis work focuses on the design and production of nanoparticle based contrast agents for signal enhancement in magnetic resonance imaging (MRI). Three different synthesis routes are explored, primarily to produce crystalline gadolinium oxide (Gd2O3) nanoparticles, and surface modification is done to obtain stable, dispersible, biocompatible probes inducing high proton relaxivities. In Paper I and II we utilized the polyol synthesis method and nanoparticle purification was performed wit...

  13. Synthesis of metal nanoparticles in living plants

    Directory of Open Access Journals (Sweden)

    Luca Marchiol

    2012-08-01

    Full Text Available In recent years, nanotechnologies have evolved from a multidisciplinary research concept to a primary scientific field. Rapid growth of new technologies has led to the development of nanoscale device components, advanced sensors, and novel biomimetic materials. In addition to chemical and physical approaches a new, simple and cheaper strategy to synthesize metal nanoparticles utilizes biological tools such as bacteria, yeasts, fungi, and plants. The majority of research has investigated ex vivo synthesis of nanoparticles in plants, proving that this method is very cost effective, and can therefore be used as an economic and valuable alternative for the large-scale production of metal nanoparticles. Instead, very few studies have been devoted to investigating the potential of living plants. The synthesis of metal nanoparticles using living plants is discussed in this review. So far, metal NPs formation in living plants has been observed for gold, silver, copper and zinc oxide. To date the results achieved demonstrate the feasibility of this process; however several aspects of the plant physiology involved should be clarified in order to be able to gain better control and modulate the formation of these new materials. Plant sciences could significantly contribute to fully exploring the potential of phyto-synthesis of metal nanoparticles.

  14. Metallic tin-based nanoparticles synthesis by laser pyrolysis: Parametric studies focused on the decreasing of the crystallite size

    International Nuclear Information System (INIS)

    Highlights: • Metallic tin-based nanoparticles were synthesized using laser pyrolysis technique. • Tetramethyltin was used as precursors whereas ethylene was the sensitizer. • The nanoparticles where covered with a tin oxidized/carbonaceous shell. • Their size where decreased by diminishing the laser beam residence time. - Abstract: Due to their characteristic to allow a continuous, one-step nanosize particles production, the laser pyrolysis technique was employed to synthesize metallic Sn-based nanoparticles using tetramethyltin vapors as precursors and ethylene as laser energy transfer agent (sensitizer). Small size of tin particles is a requirement for their use as anodes in lithium ion batteries. In order to decrease the particle size, some experimental parameters were varied, allowing the control of the crystallite size down to 30 nm. The diminishing diameter of the reactive flow injection nozzle as well as the increasing of the tin precursor vapor flow enhance the gas velocity and the decrease the reactive species residence time in the laser beam, resulting smaller tin nanodroplets which forms solid nanoparticles after rapid cooling. XRD, TEM, EDX and SAED analysis point to the formation of nanosize β-Sn particles accompanied by various amount of disordered carbon as coating provided by ethylene decomposition (associated with their polymerization/dehydrogenation) in the presence of methyl radicals from Sn(CH3)4

  15. Metallic tin-based nanoparticles synthesis by laser pyrolysis: Parametric studies focused on the decreasing of the crystallite size

    Energy Technology Data Exchange (ETDEWEB)

    Dutu, E. [National Institute for Lasers, Plasma and Radiation Physics, Lasers Dept, Bucharest—Magurele, 409, Atomistilor Street, 077125 (Romania); Dumitrache, F., E-mail: dumitracheflorian@yahoo.com [National Institute for Lasers, Plasma and Radiation Physics, Lasers Dept, Bucharest—Magurele, 409, Atomistilor Street, 077125 (Romania); “Politehnica” University of Bucharest, Physics Department, Independentei 313, Bucharest (Romania); Fleaca, C.T. [National Institute for Lasers, Plasma and Radiation Physics, Lasers Dept, Bucharest—Magurele, 409, Atomistilor Street, 077125 (Romania); “Politehnica” University of Bucharest, Physics Department, Independentei 313, Bucharest (Romania); Morjan, I.; Gavrila-Florescu, L.; Morjan, I.P.; Sandu, I.; Scarisoreanu, M.; Luculescu, C.; Niculescu, A.-M. [National Institute for Lasers, Plasma and Radiation Physics, Lasers Dept, Bucharest—Magurele, 409, Atomistilor Street, 077125 (Romania); Vasile, E. [“Politehnica” University of Bucharest, Faculty of Applied Chemistry and Material Science, Dept. of Oxide Materials and Nanomaterials, 1-7, Gh. Polizu Street, 011061 Bucharest (Romania)

    2015-05-01

    Highlights: • Metallic tin-based nanoparticles were synthesized using laser pyrolysis technique. • Tetramethyltin was used as precursors whereas ethylene was the sensitizer. • The nanoparticles where covered with a tin oxidized/carbonaceous shell. • Their size where decreased by diminishing the laser beam residence time. - Abstract: Due to their characteristic to allow a continuous, one-step nanosize particles production, the laser pyrolysis technique was employed to synthesize metallic Sn-based nanoparticles using tetramethyltin vapors as precursors and ethylene as laser energy transfer agent (sensitizer). Small size of tin particles is a requirement for their use as anodes in lithium ion batteries. In order to decrease the particle size, some experimental parameters were varied, allowing the control of the crystallite size down to 30 nm. The diminishing diameter of the reactive flow injection nozzle as well as the increasing of the tin precursor vapor flow enhance the gas velocity and the decrease the reactive species residence time in the laser beam, resulting smaller tin nanodroplets which forms solid nanoparticles after rapid cooling. XRD, TEM, EDX and SAED analysis point to the formation of nanosize β-Sn particles accompanied by various amount of disordered carbon as coating provided by ethylene decomposition (associated with their polymerization/dehydrogenation) in the presence of methyl radicals from Sn(CH{sub 3}){sub 4}.

  16. Size Controlled Synthesis of Transition Metal Nanoparticles for Catalytic Applications

    KAUST Repository

    Esparza, Angel

    2011-07-07

    Catalysis offers cleaner and more efficient chemical reactions for environmental scientists. More than 90% of industrial processes are performed with a catalyst involved, however research it is still required to improve the catalyst materials. The purpose of this work is to contribute with the development of catalysts synthesis with two different approaches. First, the precise size control of non-noble metals nanoparticles. Second, a new one-pot synthesis method based on a microemulsion system was developed to synthesize size-controlled metal nanoparticles in oxide supports. The one-pot method represents a simple approach to synthesize both support and immobilized nanometer-sized non-noble metal nanoparticles in the same reaction system. Narrow size distribution nickel, cobalt, iron and cobalt-nickel nanoparticles were obtained. High metal dispersions are attainable regardless the metal or support used in the synthesis. Thus, the methodology is adaptable and robust. The sizecontrolled supported metal nanoparticles offer the opportunity to study size effects and metal-support interactions on different catalytic reactions with different sets of metals and supports.

  17. Controllable Assembly and Separation of Colloidal Nanoparticles through a One-Tube Synthesis Based on Density Gradient Centrifugation.

    Science.gov (United States)

    Qi, Xiaohan; Li, Minglin; Kuang, Yun; Wang, Cheng; Cai, Zhao; Zhang, Jin; You, Shusen; Yin, Meizhen; Wan, Pengbo; Luo, Liang; Sun, Xiaoming

    2015-05-01

    Self-assembly of gold nanoparticles into one-dimensional (1D) nanostructures with finite primary units was achieved by introducing a thin salt (NaCl) solution layer into density gradient before centrifugation. The electrostatic interactions between Au nanoparticles would be affected and cause 1D assembly upon passing through the salt layer. A negatively charged polymer such as poly(acrylic acid) was used as an encapsulation/stabilization layer to help the formation of 1D Au assemblies, which were subsequently sorted according to unit numbers at succeeding separation zones. A centrifugal field was introduced as the external field to overcome the random Brownian motion of NPs and benefit the assembly effect. Such a facile "one-tube synthesis" approach couples assembly and separation in one centrifuge tube by centrifuging once. The method can be tuned by changing the concentration of interference salt layer, encapsulation layer, and centrifugation rate. Furthermore, positively charged fluorescent polymers such as perylenediimide-poly(N,N-diethylaminoethyl methacrylate) could encapsulate the assemblies to give tunable fluorescence properties. PMID:25809533

  18. In Situ Synthesis of Metal Nanoparticle Embedded Hybrid Soft Nanomaterials.

    Science.gov (United States)

    Divya, Kizhmuri P; Miroshnikov, Mikhail; Dutta, Debjit; Vemula, Praveen Kumar; Ajayan, Pulickel M; John, George

    2016-09-20

    The allure of integrating the tunable properties of soft nanomaterials with the unique optical and electronic properties of metal nanoparticles has led to the development of organic-inorganic hybrid nanomaterials. A promising method for the synthesis of such organic-inorganic hybrid nanomaterials is afforded by the in situ generation of metal nanoparticles within a host organic template. Due to their tunable surface morphology and porosity, soft organic materials such as gels, liquid crystals, and polymers that are derived from various synthetic or natural compounds can act as templates for the synthesis of metal nanoparticles of different shapes and sizes. This method provides stabilization to the metal nanoparticles by the organic soft material and advantageously precludes the use of external reducing or capping agents in many instances. In this Account, we exemplify the green chemistry approach for synthesizing these materials, both in the choice of gelators as soft material frameworks and in the reduction mechanisms that generate the metal nanoparticles. Established herein is the core design principle centered on conceiving multifaceted amphiphilic soft materials that possess the ability to self-assemble and reduce metal ions into nanoparticles. Furthermore, these soft materials stabilize the in situ generated metal nanoparticles and retain their self-assembly ability to generate metal nanoparticle embedded homogeneous organic-inorganic hybrid materials. We discuss a remarkable example of vegetable-based drying oils as host templates for metal ions, resulting in the synthesis of novel hybrid nanomaterials. The synthesis of metal nanoparticles via polymers and self-assembled materials fabricated via cardanol (a bioorganic monomer derived from cashew nut shell liquid) are also explored in this Account. The organic-inorganic hybrid structures were characterized by several techniques such as UV-visible spectroscopy, scanning electron microscopy (SEM), and

  19. Combined Gas-Liquid Plasma Source for Nanoparticle Synthesis

    Science.gov (United States)

    Burakov, V. S.; Kiris, V. V.; Nevar, A. A.; Nedelko, M. I.; Tarasenko, N. V.

    2016-09-01

    A gas-liquid plasma source for the synthesis of colloidal nanoparticles by spark erosion of the electrode material was developed and allowed the particle synthesis regime to be varied over a wide range. The source parameters were analyzed in detail for the electrical discharge conditions in water. The temperature, particle concentration, and pressure in the discharge plasma were estimated based on spectroscopic analysis of the plasma. It was found that the plasma parameters did not change signifi cantly if the condenser capacitance was increased from 5 to 20 nF. Purging the electrode gap with argon reduced substantially the pressure and particle concentration. Signifi cant amounts of water decomposition products in addition to electrode elements were found in the plasma in all discharge regimes. This favored the synthesis of oxide nanoparticles.

  20. Facile synthesis of monodisperse Cu{sub 3}SbSe{sub 4} nanoparticles and thermoelectric performance of Cu{sub 3}SbSe{sub 4} nanoparticle-based materials

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Yimin; Qiao, Xvsheng; Fan, Xianping, E-mail: fanxp@zju.edu.cn [Zhejiang University, State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering (China); Zhang, Xianghua [CNRS-Université de Rennes I, Laboratory of Glasses and Ceramics, Institute of Chemistry (France); Cui, Shuo; Wan, Jun [Zhejiang University, State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering (China)

    2015-07-15

    In this study, large-scale synthesis of Cu{sub 3}SbSe{sub 4} and Cu{sub 3}Sb{sub 0.98}Sn{sub 0.02}Se{sub 4} nanoparticles with a narrow size distribution was achieved through a rapid-injection route. These nanoparticles showed a monodisperse and quasi-spherical morphology. The Cu{sub 3}SbSe{sub 4} and Cu{sub 3}Sb{sub 0.98}Sn{sub 0.02}Se{sub 4} nanoparticle-based bulk materials were then prepared by hot-pressed sinter of the nanoparticles, and their thermoelectric performances were systematically studied. Due to the reduced lattice thermal conductivity from enhanced phonon scattering at the grain interfaces of the bulk materials, the maximum ZT value of the Cu{sub 3}Sb{sub 0.98}Sn{sub 0.02}Se{sub 4} bulk materials reached 0.50 at 575 K.

  1. Synthesis and characterization of functionalized magnetic nanoparticles

    Science.gov (United States)

    Biswal, Dipti; Peeples, Brianna N.; Spence, Destiny D.; Peeples, Caryn; Bell, Crystal N.; Pradhan, A. K.

    2012-04-01

    Magnetic nanoparticles have been used in a wide array of industrial and biomedical applications due to their unique properties at the nanoscale level. They are extensively used in magnetic resonance imaging (MRI), magnetic hyperthermia treatment, drug delivery, and in assays for biological separations. Furthermore, superparamagnetic nanoparticles are of large interest for in vivo applications. However, these unmodified nanoparticles aggregate and consequently lose their superparamagnetic behaviors, due to high surface to volume ratio and strong dipole to dipole interaction. For these reasons, surface coating is necessary for the enhancement and effectiveness of magnetic nanoparticles to be used in various applications. In addition to providing increased stability to the nanoparticles in different solvents or media, stabilizers such as surfactants, organic/inorganic molecules, polymer and co-polymers are employed as surface coatings, which yield magnetically responsive systems. In this work we present the synthesis and magnetic characterization of Fe3O4 nanoparticles coated with 3-aminopropyltriethoxy silane (APS) and citric acid. The particles magnetic hysteresis was measured by a superconducting quantum interference device (SQUID) magnetometer with an in-plane magnetic field. The uncoated and coated magnetic nanoparticles were characterized by using fourier transform infrared (FTIR), UV-vis, X-ray diffraction, transmission electron microscopy, and thermo-gravimetric analysis.

  2. Nanoparticle-based Sensors

    Directory of Open Access Journals (Sweden)

    V.K. Khanna

    2008-09-01

    Full Text Available Nanoparticles exhibit several unique properties that can be applied to develop chemical and biosensorspossessing desirable features like enhanced sensitivity and lower detection limits. Gold nanoparticles arecoated with sugars tailored to recognise different biological substances. When mixed with a weak solution ofthe sugar-coated nanoparticles, the target substance, e.g., ricin or E.coli, attaches to the sugar, thereby alteringits properties and changing the colour. Spores of bacterium labeled with carbon dots have been found to glowupon illumination when viewed with a confocal microscope. Enzyme/nanoparticle-based optical sensors forthe detection of organophosphate (OP compounds employ nanoparticle-modified fluorescence of an inhibitorof the enzyme to generate the signal for the OP compound detection. Nanoparticles shaped as nanoprisms,built of silver atoms, appear red on exposure to light. These nanoparticles are used as diagnostic labels thatglow when target DNA, e.g., those of anthrax or HIV, are present. Of great importance are tools like goldnanoparticle-enhanced surface-plasmon resonance sensor and silver nanoparticle surface-enhanced portableRaman integrated tunable sensor. Nanoparticle metal oxide chemiresistors using micro electro mechanical systemhotplate are very promising devices for toxic gas sensing. Chemiresistors comprising thin films of nanogoldparticles, encapsulated in monomolecular layers of functionalised alkanethiols, deposited on interdigitatedmicroelectrodes, show resistance changes through reversible absorption of vapours of harmful gases. Thispaper reviews the state-of-the-art sensors for chemical and biological terror agents, indicates their capabilitiesand applications, and presents the future scope of these devices.Defence Science Journal, 2008, 58(5, pp.608-616, DOI:http://dx.doi.org/10.14429/dsj.58.1683

  3. Laser ablation synthesis and spectral characterization of ruby nanoparticles

    Science.gov (United States)

    Baranov, M. S.; Bardina, A. A.; Savelyev, A. G.; Khramov, V. N.; Khaydukov, E. V.

    2016-04-01

    The laser ablation method was implemented for synthesis of ruby nanoparticles. Nanoparticles were obtained by nanosecond ablation of bulk ruby crystal in 10% ethanol water solution. The nanoparticles enable water colloid stability and exhibit narrow photoluminescent line at 694 nm when pumped at blue-green spectral range. The ruby nanoparticles were characterized by SEM and Z-sizer.

  4. Sunlight based irradiation strategy for rapid green synthesis of highly stable silver nanoparticles using aqueous garlic (Allium sativum) extract and their antibacterial potential

    Energy Technology Data Exchange (ETDEWEB)

    Rastogi, Lori [National Center for Chemical Characterization of Materials, Bhabha Atomic Research Centre, ECIL-PO, Hyderabad 500 062 (India); Arunachalam, J., E-mail: aruncccm@rediffmail.com [National Center for Chemical Characterization of Materials, Bhabha Atomic Research Centre, ECIL-PO, Hyderabad 500 062 (India)

    2011-09-15

    Highlights: {yields} We report green synthetic route for the production crystalline silver nanoparticles using garlic as both reducing and stabilizing agent. {yields} Synthesis has been achieved by exposing the solution mixture of [Ag(NH{sub 3}){sub 2}]{sup +} and aqueous garlic extract under sunlight. {yields} Role of light in the synthesis process has been investigated and is discussed in detail. {yields} The antibacterial effect of the synthesized silver nanoparticles has been assessed against both Gram classes of bacteria. {yields} Synthesized silver colloidal solutions were found to be stable for a very long period and retained their bactericidal potential. - Abstract: A green synthetic route for the production of highly stable silver nanoparticles using aqueous garlic extract is being reported for the first time. The silver nanoparticles were synthesized by exposing a mixture of 0.1 M [Ag(NH{sub 3}){sub 2}]{sup +} and diluted aqueous garlic extract under bright sunlight for 15 min. The garlic extract components served as both reducing and capping agents in the synthesis of silver nanoparticles while the sunlight acted as catalyst in the synthesis process. The synthesized nanoparticles were characterized using UV-visible (UV-vis) spectrophotometer; transmission electron microscopy (TEM), glancing angle X-ray diffraction (GA-XRD) and Fourier transform infra red (FTIR) spectrometry. The nanoparticles were found to be poly-dispersed in nature, spherical in shape and of 7.3 {+-} 4.4 nm in size. The FTIR analysis was suggestive of proteins as capping agents around the nanoparticles. The yield of synthesized nanoparticles was calculated to be approximately 80% by dry weight and 85% ICP-AES method. The synthesized silver nanoparticles exhibited good antibacterial potential against both Gram positive and Gram negative bacterial strains, as measured using well diffusion assay. Most importantly, the silver colloidal solutions thus synthesized were found to be stable for

  5. Sunlight based irradiation strategy for rapid green synthesis of highly stable silver nanoparticles using aqueous garlic (Allium sativum) extract and their antibacterial potential

    International Nuclear Information System (INIS)

    Highlights: → We report green synthetic route for the production crystalline silver nanoparticles using garlic as both reducing and stabilizing agent. → Synthesis has been achieved by exposing the solution mixture of [Ag(NH3)2]+ and aqueous garlic extract under sunlight. → Role of light in the synthesis process has been investigated and is discussed in detail. → The antibacterial effect of the synthesized silver nanoparticles has been assessed against both Gram classes of bacteria. → Synthesized silver colloidal solutions were found to be stable for a very long period and retained their bactericidal potential. - Abstract: A green synthetic route for the production of highly stable silver nanoparticles using aqueous garlic extract is being reported for the first time. The silver nanoparticles were synthesized by exposing a mixture of 0.1 M [Ag(NH3)2]+ and diluted aqueous garlic extract under bright sunlight for 15 min. The garlic extract components served as both reducing and capping agents in the synthesis of silver nanoparticles while the sunlight acted as catalyst in the synthesis process. The synthesized nanoparticles were characterized using UV-visible (UV-vis) spectrophotometer; transmission electron microscopy (TEM), glancing angle X-ray diffraction (GA-XRD) and Fourier transform infra red (FTIR) spectrometry. The nanoparticles were found to be poly-dispersed in nature, spherical in shape and of 7.3 ± 4.4 nm in size. The FTIR analysis was suggestive of proteins as capping agents around the nanoparticles. The yield of synthesized nanoparticles was calculated to be approximately 80% by dry weight and 85% ICP-AES method. The synthesized silver nanoparticles exhibited good antibacterial potential against both Gram positive and Gram negative bacterial strains, as measured using well diffusion assay. Most importantly, the silver colloidal solutions thus synthesized were found to be stable for a very long period (more than a year) and retained their

  6. Composite Scaffolds Based on Silver Nanoparticles for Biomedical Applications

    OpenAIRE

    Jenel Marian Patrascu; Ioan Avram Nedelcu; Maria Sonmez; Denisa Ficai; Anton Ficai; Bogdan Stefan Vasile; Camelia Ungureanu; Madalina Georgiana Albu; Bogdan Andor; Ecaterina Andronescu; Laura Cristina Rusu

    2015-01-01

    This paper presents the synthesis, characterisation, and in vitro testing of homogenous and heterogeneous materials containing silver nanoparticles (nanoAg). Three types of antiseptic materials based on collagen (COLL), hydroxyapatite (HA), and collagen/hydroxyapatite (COLL/HA) composite materials were obtained. The synthesis of silver nanoparticles was realized by chemical reaction as well as plasma sputtering deposition. The use of chemical reduction allows the synthesis of homogenous mater...

  7. Synthesis of water soluble glycine capped silver nanoparticles and their surface selective interaction

    International Nuclear Information System (INIS)

    Highlights: • Synthesis of water soluble silver nanoparticles at ambient reaction conditions. • Glycine as stabilizing agent for silver nanoparticles. • Surface selective interaction of glycine with silver nanoparticles. • Glycine concentration influences crystalinity and optical property of silver nanoparticles. - Abstract: Synthesis of biocompatible metal nanoparticles has been an area of significant interest because of their wide range of applications. In the present study, we have successfully synthesized water soluble silver nanoparticles assisted by small amino acid glycine. The method is primarily based on reduction of AgNO3 with NaBH4 in aqueous solution under atmospheric air in the presence of glycine. UV–vis spectroscopy, transmission electron microscopy (TEM), X–ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, thermogravimetry (TG) and differential thermal analysis (DTA) techniques used for characterization of resulting silver nanoparticles demonstrated that, glycine is an effective capping agent to stabilize silver nanoparticles. Surface selective interaction of glycine on (1 1 1) face of silver nanoparticles has been investigated. The optical property and crystalline behavior of silver nanoparticles were found to be sensitive to concentration of glycine. X–ray diffraction studies ascertained the phase specific interaction of glycine on silver nanoparticles. Silver nanoparticles synthesized were of diameter 60 nm. We thus demonstrated an efficient synthetic method for synthesis of water soluble silver nanoparticles capped by amino acid under mild reaction conditions with excellent reproducibility

  8. One-pot synthesis of Ag nanoparticle-coated Pb-based glass frit used in crystalline silicon solar cell

    Science.gov (United States)

    Zhou, Jian; Gan, Weiping; Tang, Hongbo; Li, Yingfen; Yang, Chao

    2015-03-01

    Deposition of Ag nanoparticles onto the surface of commercial Pb-based glass frit was conducted via a novel and facile one-pot procedure—a modified polyol process. The procedure included two steps: a 5-min pretreatment of the glass frit at 25 °C in a sonication bath and a 1-h electroless plating at 75 °C in a water bath, which only involved AgNO3 and ethylene glycol but without stabilizing agent. The silver-coated glass frit particles were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, inductively coupled plasma emission spectrometer and energy dispersive spectroscopy. It was found that the glass frit particles were homogeneously coated with dense crystalline Ag nanoparticles with an average diameter of 15 nm on the surfaces. Electrical performance of the solar cells was improved after the deposition.

  9. Synthesis of magnetite nanoparticles using electrochemical oxidation

    OpenAIRE

    Levitin, Ye. Ya.; Roy, I. D.; Kryskiv, O. S.; Chan, T.M.

    2014-01-01

    The monodisperse magnetite nanoparticles are promising for use in the biomedical industry for targeted drug delivery, cell separation and biochemical products, Magnetic Resonance Imaging, immunological studies, etc.Classic method for the synthesis of magnetite is the chemical condensation Elmore’s, it is simple and cheap, but it is complicated by the formation of side compounds which impair the magnetic properties of the final product. Biological and medical purposes require high purity magne...

  10. Lactobacillus Mediated Synthesis of Silver Oxide Nanoparticles

    OpenAIRE

    Dhoondia, Zuzer H.; Hemlatta Chakraborty

    2012-01-01

    The ability of prokaryotic microorganisms to reduce the inorganic metals has opened up an exciting eco‐friendly approach towards the development of natural ‘nano‐factories’. However, a number of issues have to be addressed from the nanotechnological and microbiological point of view before such a biosynthesis approach can compete with the existing physical and chemical methods. This report investigates the synthesis of silver oxide nanoparticles using Lactobacillus mindensis, isolated using f...

  11. Heterogeneous Photolytic Synthesis of Nanoparticles

    OpenAIRE

    Alm, Oscar

    2007-01-01

    Nanoparticles of iron, cobalt and tungsten oxide were synthesised by photolytic laser assisted chemical vapour deposition (LCVD). An excimer laser (operating at 193 nm) was used as an excitation source. The LCVD process, was monitored in situ by optical emission spectroscopy (OES). The synthesised particles were further analysed using transmission electron spectroscopy (TEM), X-ray diffraction (XRD), high resolution scanning electron microscopy (HRSEM), X-ray fluorescence spectroscopy (XRF), ...

  12. The synthesis and arrested oxidation of amorphous cobalt nanoparticles using DMSO as a functional solvent

    International Nuclear Information System (INIS)

    Magnetic nanoparticles exhibit a strong tendency to become overly oxidized and unstable during synthesis, ultimately leading to nanoparticle agglomeration and degradation. Capping agents can be used during nanoparticle synthesis to provide particle surface coverage and to improve nanoparticle dispersibility in solution, while preventing excessive oxidation and agglomeration. This paper presents a technique to synthesize amorphous 3.7 ± 1.5 nm cobalt (Co) nanoparticles using dimethyl sulfoxide (DMSO) to function as both the stabilizing agent and the solvent for Co nanoparticles via a quick, solvent-based reduction of Co2+ with NaBH4 in a DMSO solvent. UV–visible spectroscopy analysis was used to determine the minimum amount of reducing agent needed to produce Co nanoparticles so as to limit the waste of reagents. TEM and SEM imaging were used to study the morphology of the Co nanoparticles from the DMSO dispersion and of the Co nanoparticle powder. FT-IR was used to elucidate the nature of the interaction between the Co nanoparticle surface and DMSO. Furthermore, SEM–EDS elemental mapping was used to determine the composition and surface properties of the Co nanoparticles. This synthesis method demonstrates that Co nanoparticles can be successfully synthesized by simply using DMSO as a functional solvent, thereby avoiding excessive oxidation and agglomeration in solution

  13. Controlled synthesis of fluorescent silica nanoparticles inside microfluidic droplets

    OpenAIRE

    Wacker, Josias Basil; Lignos, Ioannis; Parashar, Virendra Kumar; Gijs, Martinus

    2012-01-01

    We study the droplet-based synthesis of fluorescent silica nanoparticles (50–350 nm size) in a microfluidic chip. Fluorescein-isothiocyanate (FITC) dye is first chemically linked to aminopropyl triethoxysilane (APTES) in ethanol and this reaction product is subsequently mixed with tetraethyl orthosilicate (TEOS) to yield a fluorescent silicon alkoxide precursor solution. The latter reacts with an aqueous ethanol–ammonia hydrolysing mixture inside droplets, forming fluorescent silica nanoparti...

  14. Synthesis of magnetite nanoparticles from mineral waste

    International Nuclear Information System (INIS)

    Highlights: • Mineral waste becomes a valuable source for the synthesis of magnetite. • Milling helps uniform mixing of reductant with iron ore tailings. • Magnetite nanoparticles exhibit saturation magnetization of 60 emu/g. • Ag coating induces antibacterial activity of magnetite. - Abstract: Magnetite nanoparticles were synthesized from iron ore tailings – a mineral waste collected from the iron ore processing plant. Mechanical milling followed by chemical route is employed to obtain the magnetite nanoparticles from the waste. The magnetite nanoparticles were characterized by X-ray diffractometer, Field Emission Scanning Electron Microscope, Fourier Transform Infrared Spectrometer and Vibrating Sample Magnetometer. X-ray diffraction pattern confirms the existence of a magnetite phase. Field Emission Scanning Electron Microscopic (FE-SEM) pictures reveal that the particle size is below 100 nm. Fourier Transform Infrared (FTIR) spectrum shows a band at 570 cm−1 for the Fe–O bond vibration. Vibrating Sample Magnetometric (VSM) study shows high saturation magnetization value of 60 emu/g at low applied magnetic field. Silver coated magnetite nanoparticles exhibits antibacterial property whereas bare magnetite does not

  15. Synthesis of magnetite nanoparticles from mineral waste

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Rohit [CSIR – Institute of Minerals and Materials Technology, Bhubaneswar 751 013 (India); Sakthivel, R., E-mail: velsak_r@yahoo.com [CSIR – Institute of Minerals and Materials Technology, Bhubaneswar 751 013 (India); Behura, Reshma; Mishra, B.K. [CSIR – Institute of Minerals and Materials Technology, Bhubaneswar 751 013 (India); Das, D. [UGC-DAE Consortium, Kolkata (India)

    2015-10-05

    Highlights: • Mineral waste becomes a valuable source for the synthesis of magnetite. • Milling helps uniform mixing of reductant with iron ore tailings. • Magnetite nanoparticles exhibit saturation magnetization of 60 emu/g. • Ag coating induces antibacterial activity of magnetite. - Abstract: Magnetite nanoparticles were synthesized from iron ore tailings – a mineral waste collected from the iron ore processing plant. Mechanical milling followed by chemical route is employed to obtain the magnetite nanoparticles from the waste. The magnetite nanoparticles were characterized by X-ray diffractometer, Field Emission Scanning Electron Microscope, Fourier Transform Infrared Spectrometer and Vibrating Sample Magnetometer. X-ray diffraction pattern confirms the existence of a magnetite phase. Field Emission Scanning Electron Microscopic (FE-SEM) pictures reveal that the particle size is below 100 nm. Fourier Transform Infrared (FTIR) spectrum shows a band at 570 cm{sup −1} for the Fe–O bond vibration. Vibrating Sample Magnetometric (VSM) study shows high saturation magnetization value of 60 emu/g at low applied magnetic field. Silver coated magnetite nanoparticles exhibits antibacterial property whereas bare magnetite does not.

  16. Microgravity Production of Nanoparticles of Novel Materials Using Plasma Synthesis

    Science.gov (United States)

    Frenklach, Michael; Fernandez-Pello, Carlos

    2001-01-01

    The research goal is to study the formation in reduced gravity of high quality nanoparticulate of novel materials using plasma synthesis. Particular emphasis will be placed on the production of powders of non-oxide materials like diamond, SiC, SiN, c-BN, etc. The objective of the study is to investigate the effect of gravity on plasma synthesis of these materials, and to determine how the microgravity synthesis can improve the quality and yield of the nanoparticles. It is expected that the reduced gravity will aid in the understanding of the controlling mechanisms of plasma synthesis, and will increase the yield, and quality of the synthesized powder. These materials have properties of interest in several industrial applications, such as high temperature load bearings or high speed metal machining. Furthermore, because of the nano-meter size of the particulate produced in this process, they have specific application in the fabrication of MEMS based combustion systems, and in the development and growth of nano-systems and nano-structures of these materials. These are rapidly advancing research areas, and there is a great need for high quality nanoparticles of different materials. One of the primary systems of interest in the project will be gas-phase synthesis of nanopowder of non-oxide materials.

  17. Chemically functionalized gold nanoparticles: Synthesis, characterization, and applications

    Science.gov (United States)

    Daniel, Weston Lewis

    This thesis focuses on the development and application of gold nanoparticle based detection systems and biomimetic structures. Each class of modified nanoparticle has properties that are defined by its chemical moieties that interface with solution and the gold nanoparticle core. In Chapter 2, a comparison of the biomolecular composition and binding properties of various preparations of antibody oligonucleotide gold nanoparticle conjugates is presented. These constructs differed significantly in terms of their structure and binding properties. Chapter 3 reports the use of electroless gold deposition as a light scattering signal enhancer in a multiplexed, microarray-based scanometric immunoassay using the gold nanoparticle probes evaluated in Chapter 2. The use of gold development results in greater signal enhancement than the typical silver development, and multiple rounds of metal development were found to increase the resulting signal compared to one development. Chapter 4 describes an amplified scanometric detection method for human telomerase activity. Gold nanoparticles functionalized with specific oligonucleotide sequences can efficiently capture telomerase enzymes and subsequently be elongated. Both the elongated and unmodified oligonucleotide sequences are simultaneously measured. At low telomerase concentrations, elongated strands cannot be detected, but the unmodified sequences, which come from the same probe particles, can be detected because their concentration is higher, providing a novel form of amplification. Chapter 5 reports the development of a novel colorimetric nitrite and nitrate ion assay based upon gold nanoparticle probes functionalized with Griess reaction reagents. This assay takes advantage of the distance-dependent plasmonic properties of the gold nanoparticles and the ability of nitrite ion to facilitate the cross coupling of novel nanoparticle probes. The assay works on the concept of a kinetic end point and can be triggered at the EPA

  18. Polymer and polymer-hybrid nanoparticles from synthesis to biomedical applications

    CERN Document Server

    Rangelov, Stanislav

    2013-01-01

    Polymeric and hybrid nanoparticles have received increased scientific interest in terms of basic research as well as commercial applications, promising a variety of uses for nanostructures in fields including bionanotechnology and medicine. Condensing the relevant research into a comprehensive reference, Polymer and Polymer-Hybrid Nanoparticles: From Synthesis to Biomedical Applications covers an array of topics from synthetic procedures and macromolecular design to possible biomedical applications of nanoparticles and materials based on original and unique polymers. The book presents a well-r

  19. Synthesis and evaluation of temperature- and glucose-sensitive nanoparticles based on phenylboronic acid and N-vinylcaprolactam for insulin delivery.

    Science.gov (United States)

    Wu, Jun-Zi; Bremner, David H; Li, He-Yu; Sun, Xiao-Zhu; Zhu, Li-Min

    2016-12-01

    Poly N-vinylcaprolactam-co-acrylamidophenylboronic acid p(NVCL-co-AAPBA) was prepared from N-vinylcaprolactam (NVCL) and 3-acrylamidophenylboronic acid (AAPBA), using 2,2-azobisisobutyronitrile (AIBN) as initiator. The synthesis and structure of the polymer were examined by Fourier Transform infrared spectroscopy (FT-IR) and (1)H-NMR. Dynamic light scattering (DLS), lower critical solution temperature (LCST) and transmission electron microscopy (TEM) were utilized to characterize the nanoparticles, CD spectroscopy was used to determine if there were any changes to the conformation of the insulin, and cell and animal toxicity were also investigated. The prepared nanoparticles were found to be monodisperse submicron particles and were glucose- and temperature-sensitive. In addition, the nanoparticles have good insulin-loading characteristics, do not affect the conformation of the insulin and show low-toxicity to cells and animals. These p(NVCL-co-AAPBA) nanoparticles may have some value for insulin or other hypoglycemic protein delivery. PMID:27612799

  20. Synthesis of graphene oxide based CuO nanoparticles composite electrode for highly enhanced nonenzymatic glucose detection.

    Science.gov (United States)

    Song, Jian; Xu, Lin; Zhou, Chunyang; Xing, Ruiqing; Dai, Qilin; Liu, Dali; Song, Hongwei

    2013-12-26

    CuO nanoparticles (NPs) based graphene oxide (CuO/GO) composites with different CuO NPs loading amount as well as pure CuO NPs with different hydrothermal temperatures were synthesized using a hydrothermal method. Transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and Raman spectroscopy were employed to characterize the morphology and structures of our samples. The influence of hydrothermal temperature, GO sheet, and loading amount of CuO on particle size and structure of CuO was systemically investigated. The nonenzymatic biosensing properties of CuO/GO composites and CuO NPs toward glucose were studied based on glassy carbon electrode (GCE). The sensing properties of CuO NPs were improved after loading on GO sheets. The CuO/GO composites with saturated loading of the CuO NPs exhibited the best nonenzymatic biosensing behavior. It exhibited a sensitivity of 262.52 μA mM(-1) cm(-2) to glucose with a 0.69 μM detection limit (S/N = 3) and a linear range from 2.79 μM to 2.03 mM under a working potential of +0.7 V. It also showed outstanding long term stability, good reproducibility, excellent selectivity, and accurate measurement in real serum sample. It is believed that CuO/GO composites show good promise for further application on nonenzymatic glucose biosensors. PMID:24182328

  1. Zinc Oxide Nanoparticles for Revolutionizing Agriculture: Synthesis and Applications

    Directory of Open Access Journals (Sweden)

    Sidra Sabir

    2014-01-01

    Full Text Available Nanotechnology is the most innovative field of 21st century. Extensive research is going on for commercializing nanoproducts throughout the world. Due to their unique properties, nanoparticles have gained considerable importance compared to bulk counterparts. Among other metal nanoparticles, zinc oxide nanoparticles are very much important due to their utilization in gas sensors, biosensors, cosmetics, drug-delivery systems, and so forth. Zinc oxide nanoparticles (ZnO NPs also have remarkable optical, physical, and antimicrobial properties and therefore have great potential to enhance agriculture. As far as method of formation is concerned, ZnO NPs can be synthesized by several chemical methods such as precipitation method, vapor transport method, and hydrothermal process. The biogenic synthesis of ZnO NPs by using different plant extracts is also common nowadays. This green synthesis is quite safe and ecofriendly compared to chemical synthesis. This paper elaborates the synthesis, properties, and applications of zinc oxide nanoparticles.

  2. Malva parviflora extract assisted green synthesis of silver nanoparticles

    Science.gov (United States)

    Zayed, Mervat F.; Eisa, Wael H.; Shabaka, A. A.

    2012-12-01

    Five plant leaf extracts (Malva parviflora, Beta vulgaris subsp. Vulgaris, Anethum graveolens, Allium kurrat and Capsicum frutescens) were screened for their bioreduction behavior for synthesis of silver nanoparticles. M. parviflora (Malvaceae) was found to exhibit the best reducing and protecting action in terms of synthesis rate and monodispersity of the prepared silver nanoparticles. Our measurements indicate that biosynthesis of Ag nanoparticles by M. parviflora produces Ag nanoparticles with the diameters in the range of 19-25 nm. XRD studies reveal a high degree of crystallinity and monophasic Ag nanoparticles of face-centered cubic structure. FTIR analysis proved that particles are reduced and stabilized in solution by the capping agent that is likely to be proteins secreted by the biomass. The present process is an excellent candidate for the synthesis of silver nanoparticles that is simple, easy to perform, pollutant free and inexpensive.

  3. Formation mechanism of metal nanoparticles studied by XAFS spectroscopy and effective synthesis of small metal nanoparticles

    OpenAIRE

    Tanaka, Tsunehiro; Ohyama, Junya; Teramura, Kentaro; Hitomi, Yutaka

    2012-01-01

    Recently, we studied and developed two useful synthesis methods of metal nanoparticles. The first system is wet chemical synthesis of gold nanoparticles using fast reduction. The second one is photodeposition of metal nanoparticles on TiO2. The X-ray absorption fine structure (XAFS) study revealed their unique formation mechanisms different from the conventional mechanisms. Furthermore, we designed and synthesized new multidentate protecting ligand having sulfur functional groups to synthesiz...

  4. Synthesis, purification and assembly of gold and iron oxide nanoparticles

    Science.gov (United States)

    Qiu, Penghe

    The aims of the current research include developing new synthetic strategies to prepare structurally complex gold nanoparticles and new size sorting methods to separate nanoparticles of larger size, as well as studying the assembly of nanoparticles into novel hierarchical structures through both template-assisted and template-free strategies. In the synthesis section of this dissertation (Chapters 2 & 3), a size controllable synthesis of dendritic gold nanoparticles through a seed-mediated process in ethanol is described. The effect of seeds size and shape as well as the carbon chain length of alkylamines on the formation of dendritic structure was investigated. The synthetic strategy developed is capable of forming dendritic structure on various substrates, like flat or rod-like gold particles. In another work, the shape evolution of gold nanoparticles in a seed-mediated growth as well as the kinetics of reduction of HAuCl4 in the presence of seeds was studied. The reduction of the gold precursor by sodium citrate could be greatly accelerated in the presence of seed nanoparticles. Along with the enhanced reaction kinetics, dramatic shape evolution of gold nanoparticles was observed by changing ratios of precursors. In the purification section (Chapter 4), a novel method of separating nanoparticles of different sizes in a viscosity gradient was developed. The viscosity gradient was created with polyvinylpyrrolidone (PVP) aqueous solutions. Previously, such size separation was all achieved in the density gradient, while the hidden contribution of viscosity difference inside the density gradient was not well recognized. Through this work, it is clarified that the viscosity can contribute as importantly as density in the size sorting of nanoparticles through rate zonal centrifuge. It was also demonstrated both experimentally and mathematically that the viscosity gradient is more effective in separation of larger sized nanoparticles. In the assembly section (Chapter 5

  5. Synthesis of silver nanoparticles and antibacterial property of silk fabrics treated by silver nanoparticles

    OpenAIRE

    ZHANG, GUANGYU; Liu, Yan; Gao, Xiaoliang; Chen, Yuyue

    2014-01-01

    A silver nanoparticle solution was prepared in one step by mixing AgNO3 and a multi-amino compound (RSD-NH2) solution under ambient condition. RSD-NH2 was in-house synthesized by methacrylate and polyethylene polyamine in methanol, which has abundant amino and imino groups. However, the characterization of silver nanoparticles indicated that these nanoparticles are easy to agglomerate in solution. Therefore, an in situ synthesis method of silver nanoparticles on the silk fabrics was developed...

  6. Pseudomonas deceptionensis DC5-mediated synthesis of extracellular silver nanoparticles.

    Science.gov (United States)

    Jo, Jae H; Singh, Priyanka; Kim, Yeon J; Wang, Chao; Mathiyalagan, Ramya; Jin, Chi-Gyu; Yang, Deok C

    2016-09-01

    The biological synthesis of metal nanoparticles is of great interest in the field of nanotechnology. The present work highlights the extracellular biological synthesis of silver nanoparticles using Pseudomonas deceptionensis DC5. The particles were synthesized in the culture supernatant within 48 h of incubation. Extracellular synthesis of silver nanoparticles in the culture supernatant was confirmed by ultraviolet-visible spectroscopy, which showed the absorption peak at 428 nm, and also under field emission transmission electron microscopy which displayed the spherical shape. In addition, the particles were characterized by X-ray diffraction spectroscopy, which corresponds to the crystalline nature of nanoparticles, and energy-dispersive X-ray analysis which exhibited the intense peak at 3 keV, resembling the silver nanoparticles. Further, the synthesized nanoparticles were examined by elemental mapping which displayed the dominance of the silver element in the synthesized product, and dynamic light scattering which showed the distribution of silver nanoparticles with respect to intensity, volume, and number of particles. Moreover, the silver nanoparticles have been found to be quite active in antimicrobial activity and biofilm inhibition activity against pathogenic microorganisms. Thus, the present work emphasized the prospect of using the P. deceptionensis DC5 to achieve the extracellular synthesis of silver nanoparticles in a facile and environmental manner. PMID:26232081

  7. Synthesis and optical properties of polyurethane foam modified with silver nanoparticles

    International Nuclear Information System (INIS)

    This paper for the first time describes peculiarities of synthesis of polyurethane foam modified with silver nanoparticles as a potential material for optical sensors in analytical chemistry. We found that the unique sorptional properties of polyurethane foam gave an opportunity to perform such a synthesis by two different approaches. The first one was based on sorption of previously synthesized in-solution nanoparticles by polyurethane foam, the second one consisted in preparation of nanoparticles directly in polyurethane foam matrix. This possibility is novel and interesting for practical use because the nanoparticles in polyurethane foam are capable of surface plasmon resonance. The influence of different factors during the synthesis was investigated and the optimal conditions were found. The samples prepared were characterized by diffuse reflectance spectroscopy and scanning electron microscopy. On the basis of the results obtained we first suggested that this material is attractive from the viewpoint of analytical chemistry as a convenient analytical form for determination of oxidants and reductants

  8. Size Controlled Synthesis of Starch Nanoparticles by a Microemulsion Method

    Directory of Open Access Journals (Sweden)

    Suk Fun Chin

    2014-01-01

    Full Text Available Controllable particles sizes of starch nanoparticles were synthesized via a precipitation in water-in-oil microemulsion approach. Microemulsion method offers the advantages of ultralow interfacial tension, large interfacial area, and being thermodynamically stable and affords monodispersed nanoparticles. The synthesis parameters such as stirring rates, ratios of oil/cosurfactant, oil phases, cosurfactants, and ratios of water/oil were found to affect the mean particle size of starch nanoparticles. Starch nanoparticles with mean particles sizes of 109 nm were synthesized by direct nanoprecipitation method, whereas by using precipitation in microemulsion approach, starch nanoparticles with smaller mean particles sizes of 83 nm were obtained.

  9. Marine microorganisms as potential biofactories for synthesis of metallic nanoparticles.

    Science.gov (United States)

    Manivasagan, Panchanathan; Nam, Seung Yun; Oh, Junghwan

    2016-11-01

    The use of marine microorganisms as potential biofactories for green synthesis of metallic nanoparticles is a relatively new field of research with considerable prospects. This method is eco-friendly, time saving, and inexpensive and can be easily scaled up for large-scale synthesis. The increasing need to develop simple, nontoxic, clean, and environmentally safe production methods for nanoparticles and to decrease environmental impact, minimize waste, and increase energy productivity has become important in this field. Marine microorganisms are tiny organisms that live in marine ecosystems and account for >98% of biomass of the world's ocean. Marine microorganisms synthesize metallic nanoparticles either intracellularly or extracellularly. Marine microbially-produced metallic nanoparticles have received considerable attention in recent years because of their expected impact on various applications such as medicine, energy, electronic, and space industries. The present review discusses marine microorganisms as potential biofactories for the green synthesis of metallic nanoparticles and their potential applications. PMID:26920850

  10. Nanostructured Membranes for Enzyme Catalysis and Green Synthesis of Nanoparticles

    Science.gov (United States)

    Macroporous membranes functionalized with ionizable macromolecules provide promising applications in toxic metal capture at high capacity, nanoparticle synthesis, and catalysis. Our low-pressure membrane approach is marked by reaction and separation selectivity and their tunabil...

  11. A novel perylene diimide-based tetrahedral molecule: Synthesis, characterization and self-assembly with gold nanoparticles

    Indian Academy of Sciences (India)

    Jun-bo Li; Xiang-Lin Yu; Jing Fu; Xiwen Liu; Yang Zeng

    2010-11-01

    In this study, a novel tetrahedral molecule TPPY was successfully designed and synthesized. The self-assembly of TPPY with gold nanoparticles (Au NPs) in toluene has also been investigated. The aggregation morphologies of Au NPs can be controlled to produce different aggregate structures by changing the concentration of ligand TPPY.

  12. Solid-state synthesis of monocrystalline iron oxide nanoparticle based ferrofluid suitable for magnetic resonance imaging contrast application

    Energy Technology Data Exchange (ETDEWEB)

    Lu Jun [Department of Chemical Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong (China); Yang Shihe [Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong (China); Ng, K M [Department of Chemical Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong (China); Su, C-H [Department of Chemistry and Center for Micro/Nano Science and Technology, National Cheng Kung University, Tainan 701, Taiwan (China); Yeh, C-S [Department of Chemistry and Center for Micro/Nano Science and Technology, National Cheng Kung University, Tainan 701, Taiwan (China); Wu, Y-N [Institute of Oral medicine and Center for Micro/Nano Science and Technology, National Cheng Kung University College of Medicine, Tainan 701, Taiwan (China); Shieh, D-B [Institute of Oral medicine and Center for Micro/Nano Science and Technology, National Cheng Kung University College of Medicine, Tainan 701, Taiwan (China)

    2006-12-14

    A new {gamma}-Fe{sub 2}O{sub 3} MION ferrofluid has been developed with a salt-assisted solid-state reaction. Characterizations show that the ferrofluid is composed of maghemite nanoparticles with a mean diameter of 2.7 nm. Though the nanoparticles are ultrafine, they are well crystallized, with a saturation magnetization value of 34.7 emu g{sup -1}, making them suitable for MRI applications. In spite of the absence of any surfactant, the ferrofluid can be stable for more than 6 months. An in vitro cytotoxicity test revealed good biocompatibility of the maghemite nanoparticles, suggesting that they may be further explored for biomedical applications. NMR measurements revealed significantly reduced water proton relaxation times T{sub 1} and T{sub 2}. The MR images of the nanoparticles in aqueous dispersion were investigated using a 3 T clinical MR imager. These preliminary experiments have demonstrated the potential of the as-synthesized ultrafine, cap-free maghemite MIONs in functional molecular imaging for biomedical research and clinical diagnosis.

  13. Synthesis of CZTS Nanoparticles for Low-Cost Solar Cells.

    Science.gov (United States)

    Kim, Donguk; Kim, Minha; Shim, Joongpyo; Kim, Doyoung; Choi, Wonseok; Park, Yong Seob; Choi, Youngkwan; Lee, Jaehyeong

    2016-05-01

    In this work, uniformly sized Cu2ZnSnS4 (CZTS) nanoparticles with easy control of chemical composition were synthesized and printable ink containing CZTS nanoparticles was prepared for low-cost-solar cell applications. In addition, we studied the effects of synthesis conditions, such as reaction temperature and time, on properties of the CZTS nanoparticles. For CZTS nanoparticles synthesis process, the reactants were mixed as the 2:1:1:4 molar ratios. The reaction temperature and time was varied from 220 degrees C to 320 degrees C and from 3 hours to 5 hours, respectively. The crystal structure and morphology of CZTS nanoparticles prepared under the various conditions were investigated by X-ray diffraction (XRD) and field-emission scanning electron microscopy (FE-SEM), and energy dispersive X-ray spectroscopy (EDS) was used for compositional analysis of the CZTS nanoparticles. PMID:27483876

  14. Green synthesis of gold nanoparticles using Cinnamomum zeylanicum leaf broth

    Science.gov (United States)

    Smitha, S. L.; Philip, Daizy; Gopchandran, K. G.

    2009-10-01

    Development of biologically inspired experimental processes for the synthesis of nanoparticles is an important branch of nanotechnology. The synthesis of gold nanoparticles using Cinnamomum zeylanicum leaf broth as the reducing agent is reported. The morphology of the particles formed consists of a mixture of gold nanoprisms and spheres with fcc (1 1 1) structure of gold. At lower concentrations of the extract, formation of prism shaped Au particles dominates, while at higher concentrations almost spherical particles alone are observed. Good crystallinity of the nanoparticles with fcc phase is evident from XRD patterns, clear lattice fringes in the high resolution TEM image and bright circular rings in the SAED pattern. Au nanoparticles grown are observed to be photoluminescent and the intensity of photoemission is found to increase with increase in leaf broth concentration. The ability to modulate the shape of nanoparticles as observed in this study for gold nanoparticles opens up the exciting possibility of developing further synthetic routes employing ecofriendly sources.

  15. Self-reduction and size controlled synthesis of silver nanoparticles on carbon nanospheres by grafting triazine-based molecular layer for conductivity improvement

    Science.gov (United States)

    Sang, Jing; Aisawa, Sumio; Hirahara, Hidetoshi; Kudo, Takahiro; Mori, Kunio

    2016-02-01

    A facile, self-reduction and size controlled synthesis method has been explored to fabricate silver nanoparticles (Ag NPs) on carbon nanosphere (CNs) under mild conditions. Without using predeposition of seed metals and reducing agent, a uniform and complete layer of Ag NPs was formed through grafting a molecular layer on CNs surfaces under UV irradiation. The size and thickness of Ag NPs were effectively tuned by adjusting the UV irradiation time. This direct formation of Ag NPs was attributed to self seed in aqueous Ag(NH3)2+ complex solution through a triazine-based silane coupling agent molecular layer, even at 25 °C. Scanning electron microscopy (SEM), Transmission electron microscope (TEM), and X-ray photoelectron spectroscopy (XPS) were employed to characterize the Ag NPs' properties. A substantial conductivity improvement of prepared Ag NPs on carbon nanosphere was demonstrated. The presented method is simple and environmentally friendly and thus should be of significant value for the industrial fabrication of Ag NPs on carbon nanosphere in conduct electricity paint and coating applications.

  16. Synthesis and characterization of organically linked ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Chory, Christine; Riedel, Ingo; Parisi, Juergen [Energy and Semiconductor Research Laboratory (EHF), University of Oldenburg, Carl-von Ossietzky-Strasse 9-11, 26129 Oldenburg (Germany); Kruska, Carsten; Heimbrodt, Wolfram [Department of Physics and Material Sciences Center, Philipps-University Marburg, Renthof 5, 35032 Marburg (Germany); Feser, Clemens [NEXT ENERGY - EWE Research Centre for Energy Technology e.V., Carl-von Ossietzky-Strasse 15, 26129 Oldenburg (Germany); Beenken, Wichard J.D. [Department of Theoretical Physics I, Ilmenau University of Technology, Weimarer Strasse 25, 98693 Ilmenau (Germany); Hoppe, Harald [Department of Experimental Physics I, Ilmenau University of Technology, Weimarer Strasse 32, 98693 Ilmenau (Germany)

    2012-11-15

    We report on the solution-based synthesis and characterization of three-dimensional networks of ZnO nanoparticles where the formation of structures is achieved by covalently linking the nanocrystals with bifunctional organic ligands. The colloidal synthesis will be presented with application of two ligands that vary in size and binding sites. Furthermore we report on structural characterization of dried powders and thin films by means of X-ray diffraction and electron microscopy in order to examine the regularity of the structures. We also present first investigations of the optical properties and electrical conductance behavior in lateral direction of the differently linked hybrid ZnO networks. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Ba/ZrO₂ nanoparticles as efficient heterogeneous base catalyst for the synthesis of β-nitro alcohols and 2-amino 2-chromenes

    Indian Academy of Sciences (India)

    SAGNIKA PRADHAN; KUMARI SWARNIMA; B G MISHRA

    2016-07-01

    Zirconia nanoparticles were synthesized by precipitation, urea hydrolysis, amorphous citrate and combustion synthesis methods. The zirconia surface was subsequently modified by grafting Ba²⁺ species. The Ba²⁺ modified zirconia (Ba/ZrO₂) materials were characterized using XRD, Fourier analysis, UV-vis-DRS, FESEM and HRTEM techniques. XRD study indicated selective stabilization of the tetragonal phase of zirconia in the presence of Ba²⁺ species. Fourier line profile analysis of the XRD peaks revealed that the average crystallite size of the zirconia nanoparticles is in the range of 5-15 nm. The surface area, basicity and barium content of the material depend strongly on the method of synthesis. The Ba/ZrO₂ catalyst prepared by urea hydrolysis method exhibited higher surface area and barium content compared to other samples. The catalytic activity of the Ba/ZrO₂ catalyst was evaluated for synthesis of β-nitro alcohols and 2-amino 2-chromenes. The β-nitro alcohols were synthesized by condensation of aryl aldehydes and nitromethane. Similarly, the 2-amino 2-chromenes were synthesized by condensation of arylaldehydes, α-naphthol and malononitrile. The Ba/ZrO₂ catalyst was found to be highly efficient for synthesis of both classes of compounds providing excellent yield and purity of the products.

  18. Recent progress in the synthesis of magnetic titania/iron-based, composite nanoparticles manufactured by laser pyrolysis

    Science.gov (United States)

    Fleaca, C. T.; Scarisoreanu, M.; Morjan, I.; Alexandrescu, R.; Dumitrache, F.; Luculescu, C.; Morjan, I. P.; Birjega, R.; Niculescu, A.-M.; Filoti, G.; Kuncser, V.; Vasile, E.; Danciu, V.; Popa, M.

    2014-05-01

    We report the continuous, single step synthesis of titania/iron-based magnetic nanocomposites in a single step using gas-phase laser pyrolysis technique by separately and simultaneously introducing the precursors (together with C2H4 sensitizer) in the reaction zone: Fe(CO)5 on the central flow and, using air as carrier, TiCl4 on the annular coflow. The laser power and, for the last experiment, the injection geometry were modified in order to change the Fe/Ti ratio in the resulted nanopowders. Due to the specific geometry, the reaction zone (visible as a flame) have a reductive inner central zone surrounded by and oxidative environment, allowing the formation of the metallic-carbidic iron and/or iron-doped titania and iron oxide nanophases. The raw Fe-containing nanopowders have a ferromagnetic behavior, those synthesized at higher laser power and gas velocities show significant saturation magnetization Ms values (10-12 emu/g), whereas those obtained (with higher yield and carbon content) at lower laser power and gas velocities (using wider central nozzle cross-section) have a very weak magnetization (Ms ∼ 0.05 emu/g) in spite of the higher ethylene carried Fe(CO)5 flow. The powders were annealed in air at 400 °C show lower carbon content and, for those highly Fe-doped, the hematite phase formation. Preliminary tests using UV light confirm the photocatalytic action of the annealed nanopowders in salicylic acid degradation process in solution.

  19. Flame spray pyrolysis synthesis and aerosol deposition of nanoparticle films

    DEFF Research Database (Denmark)

    Tricoli, Antonio; Elmøe, Tobias Dokkedal

    2012-01-01

    The assembly of nanoparticle films by flame spray pyrolysis (FSP) synthesis and deposition on temperature‐controlled substrates (323–723 K) was investigated for several application‐relevant conditions. An exemplary SnO2 nanoparticle aerosol was generated by FSP and its properties (e.g., particle...

  20. Recent advances in nanoparticle synthesis with reversed micelles

    OpenAIRE

    J. Eastoe; Hollamby, MJ; Hudson, L

    2006-01-01

    Synthesis of nanoparticles in microemulsions is an area of considerable current interest. This subject can be broadly divided into two sections defined by the nature of the host microemulsion reaction medium. Water-in-oil microemulsions have been used to prepare nanoparticles for more than two decades, and a wide variety of materials has been synthesised by these methods. Control parameters have been elucidated for influencing both nanoparticle concentration and morphology, allowing for tailo...

  1. Controlling Silver Nanoparticle Size and Morphology with Photostimulated Synthesis

    CERN Document Server

    Popov, A K; Langlois, R; Loth, M; Schmitz, R; Taft, G; Tanke, R S; Wruck, A

    2005-01-01

    Photo-induced synthesis and control over the size and shape of colloidal silver nanoparticles is investigated in contrast to photo-stimulated aggregation of small nanoparticles into large fractal-type structures. The feasibility of light-driven nanoengineering which enables manipulation of the sizes and shapes of the isolated nanoparticles is studied by varying the amount and type of the stabilizing agent and the type of optical irradiation.

  2. Microfluidic Reactors for the Controlled Synthesis of Monodisperse Nanoparticles

    OpenAIRE

    Erdem, Emine Yegan

    2013-01-01

    Nanoparticles have attracted a lot of attention in the past few decades due to their unique, size-dependent properties. In order to use these nanoparticles in devices or sensors effectively, it is important to maintain uniform properties throughout the system; therefore nanoparticles need to have uniform sizes - or monodisperse. In order to achieve monodispersity, an extreme control over the reaction conditions is required during their synthesis. These reaction conditions such as temperature,...

  3. Solid Lipid Nanoparticle-Based Calix[n]arenes and Calix-Resorcinarenes as Building Blocks: Synthesis, Formulation and Characterization

    OpenAIRE

    Coleman, Anthony W.; Imed Montasser; Patrick Shahgaldian; Florent Perret

    2013-01-01

    Solid lipid nanoparticles (SLNs) have attracted increasing attention during recent years. This paper presents an overview about the use of calix[n]arenes and calix-resorcinarenes in the formulation of SLNs. Because of their specific inclusion capability both in the intraparticle spaces and in the host cavities as well as their capacity for functionalization, these colloidal nanostructures represent excellent tools for the encapsulation of different active pharmaceutical ingredients (APIs) in ...

  4. Morphological transformations of silver nanoparticles in seedless photochemical synthesis

    Science.gov (United States)

    Lu, Ya; Zhang, Congyun; Hao, Rui; Zhang, Dongjie; Fu, Yizheng; Moeendarbari, Sina; Pickering, Christopher S.; Hao, Yaowu; Liu, Yaqing

    2016-05-01

    Photochemical synthesis is an easily controlled and reliable method for the fabrication of silver (Ag) nanoparticles with various morphologies. In this work, we have systematically investigated the seedless photochemical synthesis of anisotropic Ag nanoparticles with and without PVP as surface capping agent. The time evolution of anisotropic Ag nanoparticles during the synthesis process are studied using UV–visible spectra, optical images and transmission electron microscopy. The results show that the light irradiation precisely controls the start and termination of the reaction, and the presence or absence of PVP greatly affects the morphology evolution of anisotropic Ag nanoparticles. With PVP as the surface capping agent, Ag nanoparticles grow into decahedra or prism by the deposition of Ag atoms on {111} or {110} facets through epitaxial growth. However, a different morphology evolution could happen when Ag nanoparticle is synthesized without PVP as surface capping agent. In this case, Ag nanoparticles can fuse into the decahedrons through an edge-selective particle fusion mechanism, which involves attachment, rotation and realignment of Ag nanoparticles. This process was evidenced with HRTEM images at the different stages of the transformation from Ag colloid to decahedra nanoparticles. Oriented attachment and Ostwald ripening also play important role in the transformation process.

  5. Micelle based synthesis of cobalt ferrite nanoparticles and its characterization using Fourier Transform Infrared Transmission Spectrometry and Thermogravimetry

    International Nuclear Information System (INIS)

    Cobalt ferrite (CoFe2O4) nanoparticles of average size 4 nm with narrow size distribution are synthesized by reverse micelle approach. The nanoparticles are characterized using powder X-ray diffraction (XRD), Dynamic Light Scattering (DLS), Theromogravimetric analysis (TGA) and Fourier Transform Infrared Transmission Spectrometry (FTIR). Three successive transformations are observed in the thermogram that correspond to the loss of solvent and surfactant; onset of the amorphous to crystallize conversion; and isochemical transformation, i.e. migration of cations between octahedral and tetrahedral sites in the inverse spinel structure. The isochemical transformation is further confirmed by FTIR. The IR absorption bands observed at 460 and 615 cm-1 in the as-prepared CoFe2O4 nanoparticles correspond to the ferrite skeleton of octahedral and tetrahedral sites, respectively. The peak intensity at 615 and 460 cm-1 is shifted to 601 and 440 cm-1, respectively upon annealing at 320 and 400 deg. C. These results confirm migration of cations from the octahedral to the tetrahedral sites.

  6. Biomolecule mediating synthesis of inorganic nanoparticles and their applications

    Science.gov (United States)

    Wei, Zengyan

    Project 1. The conventional phage display technique focuses on screening peptide sequences that can bind on target substrates, however the selected peptides are not necessary to nucleate and mediate the growth of the target inorganic crystals, and in many cases they only show moderate affinity to the targets. Here we report a novel phage display approach that can directly screen peptides catalytically growing inorganic nanoparticles in aqueous solution at room temperature. In this study, the phage library is incubated with zinc precursor at room temperature. Among random peptide sequences displayed on phages, those phages that can grow zinc oxide (ZnO) nanoparticles are selected with centrifugation. After several rounds of selection, the peptide sequences displayed on the phage viruses are analyzed by DNA sequencing. Our screening protocol provide a simple and convenient route for the discovery of catalytic peptides that can grow inorganic nanoparticles at room temperature. This novel screening protocol can extend the method on finding a wide range of new catalysts. Project 2. Genetically engineered collagen peptides are assembled into freestanding films when quantum dots (QDs) are co-assembled as joints between collagen domains. These peptide-based films show excellent mechanical properties with Young's modulus of 20 GPa, much larger than most of the multi-composite polymer films and previously reported freestanding nanoparticle-assembled sheets, and it is even close to that reported for the bone tissue in nature. These films show little permanent deformation under small indentation while the mechanical hysteresis becomes remarkable when the load approaches near and beyond the rupture point, which is also characteristic of the bone tissue. Project 3. The shape-controlled synthesis of nanoparticles have been established in single-phase solutions by controlling growth directions of crystalline facets on seed nanocrystals kinetically; however, it is difficult to

  7. Biogenic synthesis of metallic nanoparticles and prospects toward green chemistry.

    Science.gov (United States)

    Adil, Syed Farooq; Assal, Mohamed E; Khan, Mujeeb; Al-Warthan, Abdulrahman; Siddiqui, Mohammed Rafiq H; Liz-Marzán, Luis M

    2015-06-01

    The immense importance of nanoparticles and their applications is a strong motivation for exploring new synthetic techniques. However, due to strict regulations that manage the potential environmental impacts greener alternatives for conventional synthesis are the focus of intense research. In the scope of this perspective, a concise discussion about the use of green reducing and stabilizing agents toward the preparation of metal nanoparticles is presented. Reports on the synthesis of noble metal nanoparticles using plant extracts, ascorbic acid and sodium citrate as green reagents are summarized and discussed, pointing toward an urgent need of understanding the mechanistic aspects of the involved reactions.

  8. Facile synthesis of silver nanoparticles and their application in dye degradation

    Energy Technology Data Exchange (ETDEWEB)

    Joseph, Siby, E-mail: sibyjoseph4@gmail.com [Department of Chemistry, St. George' s College, Aruvithura, Kottayam 686122, Kerala (India); Mathew, Beena, E-mail: beenamscs@gmail.com [School of Chemical Sciences, Mahatma Gandhi University, Kottayam 686560, Kerala (India)

    2015-05-15

    Graphical abstract: - Highlights: • This synthetic method uses the novel reducing agent hexamine. • The method is simple, fast and environment friendly. • This is a cost-effective method as all materials used are inexpensive and readily available. • The method provides highly stable spherical silver nanoparticles. • The nanoparticles show outstanding catalytic activity in the degradation of organic dyes. - Abstract: The present article reports a simple, facile and eco-friendly method based on microwave irradiation for the synthesis of silver nanoparticles in aqueous medium using starch as stabilizing agent and a new reducing agent namely hexamine. The silver nanoparticles were characterized by UV–vis, FTIR, XRD and HR-TEM analysis. UV–vis spectroscopic studies provided sufficient evidences for the formation of nanoparticles. The role of starch in the synthesis and stabilization of the nanoparticles was obtained from FTIR studies. The XRD and HR-TEM investigations clearly demonstrated the crystalline nature of the nanoparticles. From the TEM images, the silver nanoparticles were found to be spherical and of nearly uniform size with an average diameter of 18.2 ± 0.97 nm. The nanoparticles showed excellent catalytic activity in the degradation of methyl orange and rhodamine B by NaBH{sub 4}.

  9. Dual-mode T1 and T2 magnetic resonance imaging contrast agent based on ultrasmall mixed gadolinium-dysprosium oxide nanoparticles: synthesis, characterization, and in vivo application

    Science.gov (United States)

    Tegafaw, Tirusew; Xu, Wenlong; Wasi Ahmad, Md; Baeck, Jong Su; Chang, Yongmin; Bae, Ji Eun; Chae, Kwon Seok; Kim, Tae Jeong; Lee, Gang Ho

    2015-09-01

    A new type of dual-mode T1 and T2 magnetic resonance imaging (MRI) contrast agent based on mixed lanthanide oxide nanoparticles was synthesized. Gd3+ (8S7/2) plays an important role in T1 MRI contrast agents because of its large electron spin magnetic moment resulting from its seven unpaired 4f-electrons, and Dy3+ (6H15/2) has the potential to be used in T2 MRI contrast agents because of its very large total electron magnetic moment: among lanthanide oxide nanoparticles, Dy2O3 nanoparticles have the largest magnetic moments at room temperature. Using these properties of Gd3+ and Dy3+ and their oxide nanoparticles, ultrasmall mixed gadolinium-dysprosium oxide (GDO) nanoparticles were synthesized and their potential to act as a dual-mode T1 and T2 MRI contrast agent was investigated in vitro and in vivo. The D-glucuronic acid coated GDO nanoparticles (davg = 1.0 nm) showed large r1 and r2 values (r2/r1 ≈ 6.6) and as a result clear dose-dependent contrast enhancements in R1 and R2 map images. Finally, the dual-mode imaging capability of the nanoparticles was confirmed by obtaining in vivo T1 and T2 MR images.

  10. Green Synthesis of Calcium Oxide Nanoparticles and Its Applications

    Directory of Open Access Journals (Sweden)

    Ashwini Anantharaman

    2016-10-01

    Full Text Available Green synthesis of metal oxide nanoparticles is gaining considerable interest due to the use of environmentally friendly reactants and room temperature synthesis. This is the most preferred method of preparation as it makes use of pollution free chemicals and encourages the use of non-toxic solvents such as water and plants extracts. The present study is proposed with an objective to synthesize CaO nanoparticles by the eco-friendly green synthesis using environmentally benign papaya leaf extract and Green Tea extract. The obtained CaO nanoparticles have been characterized by UV- Vis, Fourier Transform Infrared (FTIR X-ray Diffraction (XRD, and Scanning Electron Microscopy (SEM studies. The antibacterial and photocatalytic activity of the calcium oxide nanoparticles were also analysed.

  11. DNA Nanoparticles for Improved Protein Synthesis In Vitro.

    Science.gov (United States)

    Galinis, Robertas; Stonyte, Greta; Kiseliovas, Vaidotas; Zilionis, Rapolas; Studer, Sabine; Hilvert, Donald; Janulaitis, Arvydas; Mazutis, Linas

    2016-02-24

    The amplification and digital quantification of single DNA molecules are important in biomedicine and diagnostics. Beyond quantifying DNA molecules in a sample, the ability to express proteins from the amplified DNA would open even broader applications in synthetic biology, directed evolution, and proteomics. Herein, a microfluidic approach is reported for the production of condensed DNA nanoparticles that can serve as efficient templates for in vitro protein synthesis. Using phi29 DNA polymerase and a multiple displacement amplification reaction, single DNA molecules were converted into DNA nanoparticles containing up to about 10(4)  clonal gene copies of the starting template. DNA nanoparticle formation was triggered by accumulation of inorganic pyrophosphate (produced during DNA synthesis) and magnesium ions from the buffer. Transcription-translation reactions performed in vitro showed that individual DNA nanoparticles can serve as efficient templates for protein synthesis in vitro.

  12. Direct and continuous synthesis of VO2 nanoparticles

    Science.gov (United States)

    Powell, M. J.; Marchand, P.; Denis, C. J.; Bear, J. C.; Darr, J. A.; Parkin, I. P.

    2015-11-01

    Monoclinic VO2 nanoparticles are of interest due to the material's thermochromic properties, however, direct synthesis routes to VO2 nanoparticles are often inaccessible due to the high synthesis temperatures or long reaction times required. Herein, we present a two-step synthesis route for the preparation of monoclinic VO2 nanoparticles using Continuous Hydrothermal Flow Synthesis (CHFS) followed by a short post heat treatment step. A range of particle sizes, dependent on synthesis conditions, were produced from 50 to 200 nm by varying reaction temperatures and the residence times in the process. The nanoparticles were characterised by powder X-ray diffraction, Raman and UV/Vis spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). The nanoparticles were highly crystalline with rod and sphere-like morphologies present in TEM micrographs, with the size of both the rod and spherical particles being highly dependent on both reaction temperature and residence time. SEM micrographs showed the surface of the powders produced from the CHFS process to be highly uniform. The samples were given a short post synthesis heat treatment to ensure that they were phase pure monoclinic VO2, which led to them exhibiting a large and reversible switch in optical properties (at near-IR wavelengths), which suggests that if such materials can be incorporated into coatings or in composites, they could be used for fenestration in architectural applications.

  13. Green Synthesis of Robust, Biocompatible Silver Nanoparticles Using Garlic Extract

    International Nuclear Information System (INIS)

    This paper details a facile approach for the synthesis of stable and monodisperse silver nanoparticles performed at ambient/low temperature, where Allium sativum (garlic) extract functions as the silver salt reducing agent during nanoparticle synthesis as well as the post synthesis stabilizing ligands. Varying the synthesis conditions provides control of particle size, size-distribution, and kinetics of particle formation. Infrared spectroscopy, energy dispersive X-ray chemical analysis, and high-performance liquid chromatography indicated that allicin and other carbohydrates in the garlic extract are the primary nanoparticle stabilizing moieties. The synthesized silver nanoparticles also demonstrate potential for biomedical applications, owing to (1) enhanced stability in biological media, (2) resistance to oxidation by the addition of H2O2, (3) ease and scalability of synthesis, and (4) lack of harsh chemicals required for synthesis. Cytotoxicity assays indicated no decrease in cellular proliferation for vascular smooth muscle cells and 3T3 fibroblasts at a concentration of 25 μg/mL, confirming that silver nanoparticles synthesized with garlic extract are potential candidates for future experimentation and implementation in the biomedical field.

  14. Synthesis and characterization of magnetite nanoparticles coated with lauric acid

    International Nuclear Information System (INIS)

    Understanding the process of synthesis of magnetic nanoparticles is important for its implementation in in vitro and in vivo studies. In this work we report the synthesis of magnetic nanoparticles made from ferrous oxide through coprecipitation chemical process. The nanostructured material was coated with lauric acid and dispersed in aqueous medium containing surfactant that yielded a stable colloidal suspension. The characterization of magnetic nanoparticles with distinct physico-chemical configurations is fundamental for biomedical applications. Therefore magnetic nanoparticles were characterized in terms of their morphology by means of TEM and DLS, which showed a polydispersed set of spherical nanoparticles (average diameter of ca. 9 nm) as a result of the protocol. The structural properties were characterized by using X-ray diffraction (XRD). XRD pattern showed the presence of peaks corresponding to the spinel phase of magnetite (Fe3O4). The relaxivities r2 and r2* values were determined from the transverse relaxation times T2 and T2* at 3 T. Magnetic characterization was performed using SQUID and FMR, which evidenced the superparamagnetic properties of the nanoparticles. Thermal characterization using DSC showed exothermic events associated with the oxidation of magnetite to maghemite. - Highlights: • Synthesis of magnetic nanoparticles coated with lauric acid • Characterization of magnetic nanoparticles • Morphological, structural, magnetic, calorimetric and relaxometric characterization

  15. Synthesis and characterization of magnetite nanoparticles coated with lauric acid

    Energy Technology Data Exchange (ETDEWEB)

    Mamani, J.B., E-mail: javierbm@einstein.br [Instituto do Cérebro-InCe, Hospital Israelita Albert Einstein-HIAE, 05651-901 São Paulo (Brazil); Costa-Filho, A.J. [Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto (Brazil); Cornejo, D.R. [Instituto de Física Universidade de São Paulo, USP, São Paulo (Brazil); Vieira, E.D. [Instituto de Física, Universidade Federal de Goiás, Goiânia (Brazil); Gamarra, L.F. [Instituto do Cérebro-InCe, Hospital Israelita Albert Einstein-HIAE, 05651-901 São Paulo (Brazil)

    2013-07-15

    Understanding the process of synthesis of magnetic nanoparticles is important for its implementation in in vitro and in vivo studies. In this work we report the synthesis of magnetic nanoparticles made from ferrous oxide through coprecipitation chemical process. The nanostructured material was coated with lauric acid and dispersed in aqueous medium containing surfactant that yielded a stable colloidal suspension. The characterization of magnetic nanoparticles with distinct physico-chemical configurations is fundamental for biomedical applications. Therefore magnetic nanoparticles were characterized in terms of their morphology by means of TEM and DLS, which showed a polydispersed set of spherical nanoparticles (average diameter of ca. 9 nm) as a result of the protocol. The structural properties were characterized by using X-ray diffraction (XRD). XRD pattern showed the presence of peaks corresponding to the spinel phase of magnetite (Fe{sub 3}O{sub 4}). The relaxivities r{sub 2} and r{sub 2}* values were determined from the transverse relaxation times T{sub 2} and T{sub 2}* at 3 T. Magnetic characterization was performed using SQUID and FMR, which evidenced the superparamagnetic properties of the nanoparticles. Thermal characterization using DSC showed exothermic events associated with the oxidation of magnetite to maghemite. - Highlights: • Synthesis of magnetic nanoparticles coated with lauric acid • Characterization of magnetic nanoparticles • Morphological, structural, magnetic, calorimetric and relaxometric characterization.

  16. Biological Synthesis of Nanoparticles from Plants and Microorganisms.

    Science.gov (United States)

    Singh, Priyanka; Kim, Yu-Jin; Zhang, Dabing; Yang, Deok-Chun

    2016-07-01

    Nanotechnology has become one of the most promising technologies applied in all areas of science. Metal nanoparticles produced by nanotechnology have received global attention due to their extensive applications in the biomedical and physiochemical fields. Recently, synthesizing metal nanoparticles using microorganisms and plants has been extensively studied and has been recognized as a green and efficient way for further exploiting microorganisms as convenient nanofactories. Here, we explore and detail the potential uses of various biological sources for nanoparticle synthesis and the application of those nanoparticles. Furthermore, we highlight recent milestones achieved for the biogenic synthesis of nanoparticles by controlling critical parameters, including the choice of biological source, incubation period, pH, and temperature.

  17. Synthesis and deposition of metal nanoparticles by gas condensation process

    Energy Technology Data Exchange (ETDEWEB)

    Maicu, Marina, E-mail: marina.maicu@fep.fraunhofer.de; Glöß, Daniel; Frach, Peter [Fraunhofer Institut für Elektronenstrahl und Plasmatechnik, FEP, Winterbergstraße 28, 01277 Dresden (Germany); Schmittgens, Ralph; Gerlach, Gerald [Institut für Festkörperelektronik, IFE, TU Dresden, Helmholtz Straße 18, 01069 Dresden (Germany); Hecker, Dominic [Fraunhofer Institut für Elektronenstrahl und Plasmatechnik, FEP, Winterbergstraße 28, 01277 Dresden, Germany and Institut für Festkörperelektronik, IFE, TU Dresden, Helmholtz Straße 18, 01069 Dresden (Germany)

    2014-03-15

    In this work, the synthesis of Pt and Ag nanoparticles by means of the inert gas phase condensation of sputtered atomic vapor is presented. The process parameters (power, sputtering time, and gas flow) were varied in order to study the relationship between deposition conditions and properties of the nanoparticles such as their quantity, size, and size distribution. Moreover, the gas phase condensation process can be combined with a plasma enhanced chemical vapor deposition procedure in order to deposit nanocomposite coatings consisting of metallic nanoparticles embedded in a thin film matrix material. Selected examples of application of the generated nanoparticles and nanocomposites are discussed.

  18. Polymer-Nanoparticle Composites: From Synthesis to Modern Applications

    Directory of Open Access Journals (Sweden)

    Thomas Hanemann

    2010-05-01

    Full Text Available The addition of inorganic spherical nanoparticles to polymers allows the modification of the polymers physical properties as well as the implementation of new features in the polymer matrix. This review article covers considerations on special features of inorganic nanoparticles, the most important synthesis methods for ceramic nanoparticles and nanocomposites, nanoparticle surface modification, and composite formation, including drawbacks. Classical nanocomposite properties, as thermomechanical, dielectric, conductive, magnetic, as well as optical properties, will be summarized. Finally, typical existing and potential applications will be shown with the focus on new and innovative applications, like in energy storage systems.

  19. Green synthesis and characterization of palladium nanoparticles and its conjugates from solanum trilobatum leaf extract

    Institute of Scientific and Technical Information of China (English)

    Amarnath Kanchana; Saveetha Devarajan

    2010-01-01

    An important area of research in nanotechnology deals with the synthesis of nanoparticles of different chemical compositions, sizes and controlled monodispersity. Currently, there is a growing need to develop environmentally benign nanoparticle synthesis in which no toxic chemicals are used in the synthesis protocol. Palladium nanoparticles (PdNp) are of interest because of their catalytic properties and affinity for hydrogen. Our protocol for the phyto-synthesis of PdNp under moderate pH and room temperature offers a new means to develop environmentally benign nanoparticles. Solanum trilobatum is enlightened in our present study as it is enriched with phytochemicals to reduce palladium chloride ions. Poly MVA a dietary supplement based on the nontoxic chemotherapeutic lipoic acid-palladium complex (LA-Pd) is been hypothesized as the new paradigm of cancer therapy. Hence forth we successfully conjugated lipoic acid (S-PdNp-LA) and vitamins (S-PdNp-Vitamin-LA) to palladium nanoparticles synthesised from Solanum trilobatum leaf extract. These nanoparticles (S-PdNp, S-PdNp-LA, S-PdNp-Vitamin-LA) were characterized with UV-Vis Spectroscopy, SEM and FTIR analysis, which revealed that S-PdNp are polydisperse and of different morphologies ranging from 60~70 nm (S-PdNp), 65~80 nm (S-PdNp-LA) and 75~100 nm (S-PdNp-Vitamin-LA) in size.

  20. Synthesis of silver nanoparticles in hydrogels crosslinked by ionizing radiation

    Energy Technology Data Exchange (ETDEWEB)

    Alcantara, Maria Tania S.; Oliani, Washington L.; Brant, Antonio J.C.; Oliveira, Maria Jose A. de; Riella, Humberto Gracher; Lugao, Ademar B., E-mail: maratalcantara@uol.com.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    Hydrogel is defined as a polymeric material which exhibits the ability to swell and retain a significant fraction of water within its structure without dissolving the polymeric network. Silver nanoparticles (AgNPs) are used in a range of medicinal products based on hydrogels and diverse other products due to their antibacterial properties at low concentrations. The use of ionizing radiation in the production process of hydrogels of poly(N-vinyl-2-pyrrolidone) (PVP) and poly(vinyl alcohol) (PVA) in aqueous solutions enables the crosslinking of their polymer chains. If polymer solutions contain Ag{sup +} ions, these can be reduced radiolytically to nanocrystalline silver. The objective of this study was to investigate the reduction of Ag{sup +} ions by gamma-irradiation for the synthesis of AgNPs in hydrogels of PVA and PVP as main polymers and to make a comparison of the performance of the two polymeric matrices, chiefly focusing on the effect of the AgNPs' synthesis on the crosslinking of both polymers. The properties of the hydrogel matrices obtained were evaluated from tests of gel fraction, swelling in water, and stress-strain. The results of mechanical properties of PVA matrix were higher than those of PVP one whereas the latter exhibited a higher swelling degree. The reduction of silver ions was confirmed by UV-visible absorption spectrum, whose characteristics also indicated the formation of silver nanoparticles in both arrays. (author)

  1. Solid Lipid Nanoparticle-Based Calix[n]arenes and Calix-Resorcinarenes as Building Blocks: Synthesis, Formulation and Characterization

    Directory of Open Access Journals (Sweden)

    Anthony W. Coleman

    2013-11-01

    Full Text Available Solid lipid nanoparticles (SLNs have attracted increasing attention during recent years. This paper presents an overview about the use of calix[n]arenes and calix-resorcinarenes in the formulation of SLNs. Because of their specific inclusion capability both in the intraparticle spaces and in the host cavities as well as their capacity for functionalization, these colloidal nanostructures represent excellent tools for the encapsulation of different active pharmaceutical ingredients (APIs in the area of drug targeting, cosmetic additives, contrast agents, etc. Various synthetic routes to the supramolecular structures will be given. These various routes lead to the formulation of the corresponding SLNs. Characterization, properties, toxicological considerations as well as numerous corresponding experimental studies and analytical methods will be also exposed and discussed.

  2. Synthesis of self-assembly plasmonic silver nanoparticles with tunable luminescence color

    Energy Technology Data Exchange (ETDEWEB)

    Al-Ghamdi, Haifa S.; Mahmoud, Waleed E., E-mail: w_e_mahmoud@yahoo.com

    2014-01-15

    Assembly is an elegant and effective bottom-up approach to prepare arrays of nanoparticles from nobel metals. Noble metal nanoparticles are perfect building blocks because they can be prepared with an adequate functionalization to allow their assembly and with controlled sizes. Herein, we report a novel recipe for the synthesis of self-assembled silver nanoparticles with tunable optical properties and sizes. The synthetic route followed here based on the covalent binding among silver nanoparticles by means of poly vinyl alcohol for the first time. The size of silver nanoparticle is governed by varying the amount of sodium borohydride. The as-synthesized nanoparticles were characterized by transmission electron microscopy, x-ray diffraction, energy dispersive x-ray spectroscopy, selected area electron diffraction and UV–vis spectroscopy. Results depicted that self-assembly of mono-dispersed silver nanoparticles with different sizes have been achieved. The silver nanostructure has a single crystalline faced centered cubic structure with growth orientation along (1 1 1) facet. These nanoparticles exhibited localized surface plasmon resonance at 403 nm. The luminescence peaks were red-sifted from violet to green due to the increase of the particle sizes. -- Highlights: • Self-assembled silver nanoparticles based PVA were synthesized. • NaBH{sub 4} amount was found particle size dependent. • Silver nanoparticles strongly affected the surface plasmon resonance. • Highly symmetric luminescence emission band narrow width is obtained. • Dark field image showed a tunable color change from violet to green.

  3. Yolk/shell nanoparticles: classifications, synthesis, properties, and applications.

    Science.gov (United States)

    Purbia, Rahul; Paria, Santanu

    2015-12-21

    Core/shell nanoparticles were first reported in the early 1990s with a simple spherical core and shell structure, but the area is gradually diversifying in multiple directions such as different shapes, multishells, yolk/shell etc., because of the development of different new properties of the materials, which are useful for several advanced applications. Among different sub-areas of core/shell nanoparticles, yolk/shell nanoparticles (YS NPs) have drawn significant attention in recent years because of their unique properties such as low density, large surface area, ease of interior core functionalization, a good molecular loading capacity in the void space, tunable interstitial void space, and a hollow outer shell. The YS NPs have better properties over simple core/shell or hollow NPs in various fields including biomedical, catalysis, sensors, lithium batteries, adsorbents, DSSCs, microwave absorbers etc., mainly because of the presence of free void space, porous hollow shell, and free core surface. This review presents an extensive classification of YS NPs based on their structures and types of materials, along with synthesis strategies, properties, and applications with which one would be able to draw a complete picture of this area.

  4. Yolk/shell nanoparticles: classifications, synthesis, properties, and applications

    Science.gov (United States)

    Purbia, Rahul; Paria, Santanu

    2015-11-01

    Core/shell nanoparticles were first reported in the early 1990s with a simple spherical core and shell structure, but the area is gradually diversifying in multiple directions such as different shapes, multishells, yolk/shell etc., because of the development of different new properties of the materials, which are useful for several advanced applications. Among different sub-areas of core/shell nanoparticles, yolk/shell nanoparticles (YS NPs) have drawn significant attention in recent years because of their unique properties such as low density, large surface area, ease of interior core functionalization, a good molecular loading capacity in the void space, tunable interstitial void space, and a hollow outer shell. The YS NPs have better properties over simple core/shell or hollow NPs in various fields including biomedical, catalysis, sensors, lithium batteries, adsorbents, DSSCs, microwave absorbers etc., mainly because of the presence of free void space, porous hollow shell, and free core surface. This review presents an extensive classification of YS NPs based on their structures and types of materials, along with synthesis strategies, properties, and applications with which one would be able to draw a complete picture of this area.

  5. A novel bacterial isolate Stenotrophomonas maltophilia as living factory for synthesis of gold nanoparticles

    Directory of Open Access Journals (Sweden)

    Shekhawat G

    2009-07-01

    Full Text Available Abstract Background The synthesis of gold nanoparticles (GNPs has received considerable attention with their potential applications in various life sciences related applications. Recently, there has been tremendous excitement in the study of nanoparticles synthesis by using some natural biological system, which has led to the development of various biomimetic approaches for the growth of advanced nanomaterials. In the present study, we have demonstrated the synthesis of gold nanoparticles by a novel bacterial strain isolated from a site near the famous gold mines in India. A promising mechanism for the biosynthesis of GNPs by this strain and their stabilization via charge capping was investigated. Results A bacterial isolate capable of gold nanoparticle synthesis was isolated and identified as a novel strain of Stenotrophomonas malophilia (AuRed02 based on its morphology and an analysis of its 16S rDNA gene sequence. After 8 hrs of incubation, monodisperse preparation of gold nanoparticles was obtained. Gold nanoparticles were characterized and found to be of ~40 nm size. Electrophoresis, Zeta potential and FTIR measurements confirmed that the particles are capped with negatively charged phosphate groups from NADP rendering them stable in aqueous medium. Conclusion The process of synthesis of well-dispersed nanoparticles using a novel microorganism isolated from the gold enriched soil sample has been reported in this study, leading to the development of an easy bioprocess for synthesis of GNPs. This is the first study in which an extensive characterization of the indigenous bacterium isolated from the actual gold enriched soil was conducted. Promising mechanism for the biosynthesis of GNPs by the strain and their stabilization via charge capping is suggested, which involves an NADPH-dependent reductase enzyme that reduces Au3+ to Au0 through electron shuttle enzymatic metal reduction process.

  6. Green Synthesis of Hydroxyethyl Cellulose-Stabilized Silver Nanoparticles

    Directory of Open Access Journals (Sweden)

    M. A. El-Sheikh

    2013-01-01

    Full Text Available Green synthesis aims to minimize the use of unsafe reactants and maximize the efficiency of synthesis process. These could be achieved by using environmentally compassionate polymers and nontoxic chemicals. Hydroxyethyl cellulose (HEC, an ecofriendly polymer, was used as both reducing and stabilizing agents in the synthesis of stable silver nanoparticles, while silver nitrate was used as a precursor and water as a solvent. The formation of silver nanoparticles was assessed by monitoring UV-vis spectra of the silver colloidal solution. The size of the nanoparticles was measured using transmission electron microscope (TEM. Reaction kinetics was followed by measuring the absorbance of silver colloidal solution at different time intervals. Optimum reaction conditions revealed that the highest absorbance was obtained using HEC : AgNO3 of 1.5 : 0.17 (g/100 cm3 at 70°C for 120 min at pH 12. The Ag0 nanoparticles colloidal solution so obtained (1000 ppm were found stable in aqueous solution over a period of six months at room temperature (°C. The sizes of these nanoparticles were found in the range of 11–60 nm after six months of storing. FTIR spectra confirmed the interaction of both the aldehyde and OH groups in the synthesis and stabilization of silver nanoparticles.

  7. Hydrothermal synthesis and physicochemical properties of ruthenium(0) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Dikhtiarenko, A., E-mail: dikhtiarenkoalla@uniovi.es [Departamento de Quimica Organica e Inorganica, Universidad de Oviedo - CINN, 33006 Oviedo (Spain); Khainakov, S.A.; Garcia, J.R.; Gimeno, J. [Departamento de Quimica Organica e Inorganica, Universidad de Oviedo - CINN, 33006 Oviedo (Spain); Pedro, I. de; Fernandez, J. Rodriguez [CITIMAC, Facultad de Ciencias, Universidad de Cantabria, 39005 Santander (Spain); Blanco, J.A. [Departamento de Fisica, Universidad de Oviedo, 33007 Oviedo (Spain)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer Ruthenium nanoparticles were synthesized by hydrothermal technique. Black-Right-Pointing-Pointer The average size of the nanoparticles are depend on the reducing agent used. Black-Right-Pointing-Pointer The magnetic response seems to be dominated by a paramagnetic contribution characteristic of the band electronic magnetism of the ruthenium(0) nanoparticles. - Abstract: The synthesis of ruthenium nanoparticles in hydrothermal conditions using mild reducing agents (succinic acid, ascorbic acid and sodium citrate) is reported. The shape of the nanoparticles depends on the type of the reducing agent, while the size is more influenced by the pH of the medium. The magnetic response seems to be dominated by a paramagnetic contribution characteristic of the band electronic magnetism of the nanoparticles.

  8. Template-Assisted Synthesis and Characterization of Passivated Nickel Nanoparticles

    Science.gov (United States)

    Veena Gopalan, E.; Malini, K. A.; Santhoshkumar, G.; Narayanan, T. N.; Joy, P. A.; Al-Omari, I. A.; Sakthi Kumar, D.; Yoshida, Yasuhiko; Anantharaman, M. R.

    2010-05-01

    Potential applications of nickel nanoparticles demand the synthesis of self-protected nickel nanoparticles by different synthesis techniques. A novel and simple technique for the synthesis of self-protected nickel nanoparticles is realized by the inter-matrix synthesis of nickel nanoparticles by cation exchange reduction in two types of resins. Two different polymer templates namely strongly acidic cation exchange resins and weakly acidic cation exchange resins provided with cation exchange sites which can anchor metal cations by the ion exchange process are used. The nickel ions which are held at the cation exchange sites by ion fixation can be subsequently reduced to metal nanoparticles by using sodium borohydride as the reducing agent. The composites are cycled repeating the loading reduction cycle involved in the synthesis procedure. X-Ray Diffraction, Scanning Electron Microscopy, Transmission Electron microscopy, Energy Dispersive Spectrum, and Inductively Coupled Plasma Analysis are effectively utilized to investigate the different structural characteristics of the nanocomposites. The hysteresis loop parameters namely saturation magnetization and coercivity are measured using Vibrating Sample Magnetometer. The thermomagnetization study is also conducted to evaluate the Curie temperature values of the composites. The effect of cycling on the structural and magnetic characteristics of the two composites are dealt in detail. A comparison between the different characteristics of the two nanocomposites is also provided.

  9. Template-Assisted Synthesis and Characterization of Passivated Nickel Nanoparticles

    Directory of Open Access Journals (Sweden)

    Al-Omari IA

    2010-01-01

    Full Text Available Abstract Potential applications of nickel nanoparticles demand the synthesis of self-protected nickel nanoparticles by different synthesis techniques. A novel and simple technique for the synthesis of self-protected nickel nanoparticles is realized by the inter-matrix synthesis of nickel nanoparticles by cation exchange reduction in two types of resins. Two different polymer templates namely strongly acidic cation exchange resins and weakly acidic cation exchange resins provided with cation exchange sites which can anchor metal cations by the ion exchange process are used. The nickel ions which are held at the cation exchange sites by ion fixation can be subsequently reduced to metal nanoparticles by using sodium borohydride as the reducing agent. The composites are cycled repeating the loading reduction cycle involved in the synthesis procedure. X-Ray Diffraction, Scanning Electron Microscopy, Transmission Electron microscopy, Energy Dispersive Spectrum, and Inductively Coupled Plasma Analysis are effectively utilized to investigate the different structural characteristics of the nanocomposites. The hysteresis loop parameters namely saturation magnetization and coercivity are measured using Vibrating Sample Magnetometer. The thermomagnetization study is also conducted to evaluate the Curie temperature values of the composites. The effect of cycling on the structural and magnetic characteristics of the two composites are dealt in detail. A comparison between the different characteristics of the two nanocomposites is also provided.

  10. Plasma Synthesis of Nanoparticles for Nanocomposite Energy Applications

    Energy Technology Data Exchange (ETDEWEB)

    Peter C. Kong; Alex W. Kawczak

    2008-09-01

    The nanocomposite energy applications for plasma reactor produced nanoparticles are reviewed. Nanoparticles are commonly defined as particles less than 100 nm in diameter. Due to this small size, nanoparticles have a high surface-to-volume ratio. This increases the surface energy compared to the bulk material. The high surface-to-volume ratio and size effects (quantum effects) give nanoparticles distinctive chemical, electronic, optical, magnetic and mechanical properties from those of the bulk material. Nanoparticles synthesis can be grouped into 3 broad approaches. The first one is wet phase synthesis (sol-gel processing), the second is mechanical attrition, and the third is gas-phase synthesis (aerosol). The properties of the final product may differ significantly depending on the fabrication route. Currently, there are no economical large-scale production processes for nanoparticles. This hinders the widespread applications of nanomaterials in products. The Idaho National Laboratory (INL) is engaging in research and development of advanced modular hybrid plasma reactors for low cost production of nanoparticles that is predicted to accelerate application research and enable the formation of technology innovation alliances that will result in the commercial production of nanocomposites for alternative energy production devices such as fuel cells, photovoltaics and electrochemical double layer capacitors.

  11. Facile Synthesis of Copper Oxide Nanoparticles via Electrospinning

    Directory of Open Access Journals (Sweden)

    Abdullah Khalil

    2014-01-01

    Full Text Available A novel approach for synthesizing copper oxide (CuO nanoparticles (NPs through electrospinning is reported. The approach is based on producing rough and discontinuous electrospun nanofibers from a precursor based on copper acetate salt and polyvinyl alcohol (PVA polymer. Selectively removing the polymeric phase from the fibers produced highly rough CuO nanofibers, which were composed of NPs that are weakly held together in a one-dimensional (1D manner. Sonication in a suitable liquid under controlled conditions completely disintegrated the nanofibers into NPs, resulting in the formation of uniform CuO NPs suspension. Aberration corrected high resolution transmission electron microscope (HRTEM showed that the obtained NPs are highly crystalline and nearly sphere-like with a diameter of 30 to 70 nm. Thus, electrospinning, which is a low cost and industrially scalable technique, can also be employed for economic and large scale synthesis of NPs.

  12. Microbial synthesis of Flower-shaped gold nanoparticles.

    Science.gov (United States)

    Singh, Priyanka; Kim, Yeon Ju; Wang, Chao; Mathiyalagan, Ramya; Yang, Deok Chun

    2016-09-01

    The shape of nanoparticles has been recognized as an important attribute that determines their applicability in various fields. The flower shape (F-shape) has been considered and is being focused on, because of its enhanced properties when compared to the properties of the spherical shape. The present study proposed the microbial synthesis of F-shaped gold nanoparticles within 48 h using the Bhargavaea indica DC1 strain. The F-shaped gold nanoparticles were synthesized extracellularly by the reduction of auric acid in the culture supernatant of B. indica DC1. The shape, size, purity, and crystalline nature of F-shaped gold nanoparticles were revealed by various instrumental techniques including UV-Vis, FE-TEM, EDX, elemental mapping, XRD, and DLS. The UV-Vis absorbance showed a maximum peak at 536 nm. FE-TEM revealed the F-shaped structure of nanoparticles. The EDX peak obtained at 2.3 keV indicated the purity. The peaks obtained on XRD analysis corresponded to the crystalline nature of the gold nanoparticles. In addition, the results of elemental mapping indicated the maximum distribution of gold elements in the nanoproduct obtained. Particle size analysis revealed that the average diameter of the F-shaped gold nanoparticles was 106 nm, with a polydispersity index (PDI) of 0.178. Thus, the methodology developed for the synthesis of F-shaped gold nanoparticles is completely green and economical. PMID:25943137

  13. Gelatine-assisted synthesis of magnetite nanoparticles for magnetic hyperthermia

    Energy Technology Data Exchange (ETDEWEB)

    Alves, André F.; Mendo, Sofia G. [Universidade de Lisboa, Centro de Química e Bioquímica, Faculdade de Ciências (Portugal); Ferreira, Liliana P. [Universidade de Lisboa, Biosystems and Integrative Sciences Institute, Faculdade de Ciências (Portugal); Mendonça, Maria Helena [Universidade de Lisboa, Centro de Química e Bioquímica, Faculdade de Ciências (Portugal); Ferreira, Paula [University of Aveiro, Department of Materials and Ceramic Engineering, CICECO - Aveiro Institute of Materials (Portugal); Godinho, Margarida; Cruz, Maria Margarida [Universidade de Lisboa, Biosystems and Integrative Sciences Institute, Faculdade de Ciências (Portugal); Carvalho, Maria Deus, E-mail: mdcarvalho@ciencias.ulisboa.pt [Universidade de Lisboa, Centro de Química e Bioquímica, Faculdade de Ciências (Portugal)

    2016-01-15

    Magnetite nanoparticles were synthesized by the co-precipitation method exploring the use of gelatine and agar as additives. For comparison, magnetite nanoparticles were also prepared by standard co-precipitation, by co-precipitation with the addition of a surfactant (sodium dodecyl sulphate) and by the thermal decomposition method. The structure and morphology of the synthesized nanoparticles were investigated by powder X-ray diffraction and transmission electron microscopy. Their magnetic properties were studied by SQUID magnetometry and {sup 57}Fe Mössbauer spectroscopy. The nanoparticles potential for applications in magnetic hyperthermia was evaluated through heating efficiency under alternating magnetic field. The results show that all synthesis methods produce Fe{sub 3−x}O{sub 4} nanoparticles with similar sizes. The nanoparticles synthesized in the gelatine medium display the narrowest particle size distribution, the lowest oxidation degree, one of the highest saturation magnetization values and the best hyperthermia efficiency, proving that this gelatine-assisted synthesis is an efficient, environmental friendly, and low-cost method to produce magnetite nanoparticles. Graphical Abstract: A new gelatine-assisted method is an efficient and low-cost way to synthesize magnetite nanoparticles with enhanced magnetic hyperthermia.

  14. Size Controlled Synthesis of Starch Nanoparticles by a Microemulsion Method

    OpenAIRE

    2014-01-01

    Controllable particles sizes of starch nanoparticles were synthesized via a precipitation in water-in-oil microemulsion approach. Microemulsion method offers the advantages of ultralow interfacial tension, large interfacial area, and being thermodynamically stable and affords monodispersed nanoparticles. The synthesis parameters such as stirring rates, ratios of oil/cosurfactant, oil phases, cosurfactants, and ratios of water/oil were found to affect the mean particle size of starch nanoparti...

  15. Prodigious Effects of Concentration Intensification on Nanoparticle Synthesis: A High-Quality, Scalable Approach.

    Science.gov (United States)

    Williamson, Curtis B; Nevers, Douglas R; Hanrath, Tobias; Robinson, Richard D

    2015-12-23

    Realizing the promise of nanoparticle-based technologies demands more efficient, robust synthesis methods (i.e., process intensification) that consistently produce large quantities of high-quality nanoparticles (NPs). We explored NP synthesis via the heat-up method in a regime of previously unexplored high concentrations near the solubility limit of the precursors. We discovered that in this highly concentrated and viscous regime the NP synthesis parameters are less sensitive to experimental variability and thereby provide a robust, scalable, and size-focusing NP synthesis. Specifically, we synthesize high-quality metal sulfide NPs (200 g) relative to the current field of large-scale (0.1-5 g yields) and laboratory-scale (Ostwald ripening. PMID:26592380

  16. Composite Scaffolds Based on Silver Nanoparticles for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    Jenel Marian Patrascu

    2015-01-01

    Full Text Available This paper presents the synthesis, characterisation, and in vitro testing of homogenous and heterogeneous materials containing silver nanoparticles (nanoAg. Three types of antiseptic materials based on collagen (COLL, hydroxyapatite (HA, and collagen/hydroxyapatite (COLL/HA composite materials were obtained. The synthesis of silver nanoparticles was realized by chemical reaction as well as plasma sputtering deposition. The use of chemical reduction allows the synthesis of homogenous materials while the plasma sputtering deposition can be easily used for the synthesis of homogeneous and heterogeneous support. Based on the in vitro assays clear antiseptic activity against Escherichia coli was relieved even at low content of nanoAg (10 ppm.

  17. Synthesis of silver nanoparticles using leaves of Catharanthus roseus Linn. G. Don and their antiplasmodial activities

    Directory of Open Access Journals (Sweden)

    S Ponarulselvam

    2012-07-01

    Conclusions: It can be concluded that the leaves of C. roseus can be good source for synthesis of silver nanoparticle which shows antiplasmodial activity against P. falciparum. The important outcome of the study will be the development of value added products from medicinal plants C. roseus for biomedical and nanotechnology based industries.

  18. Chitosan nanoparticles synthesis caught in action using microdroplet reactions.

    Science.gov (United States)

    Kamat, Vivek; Bodas, Dhananjay; Paknikar, Kishore

    2016-01-01

    The ionic gelation process for the synthesis of chitosan nanoparticles was carried out in microdroplet reactions. The synthesis could be stopped instantaneously at different time points by fast dilution of the reaction mixture with DI water. Using this simple technique, the effect of temperature and reactant concentrations on the size and distribution of the nanoparticles formed, as a function of time, could be investigated by DLS and SEM. Results obtained indicated very early (1-5 s) nucleation of the particles followed by growth. The concentration of reactants, reaction temperature as well as time, were found to (severally and collectively) determine the size of nanoparticles and their distribution. Nanoparticles obtained at 4 °C were smaller (60-80 nm) with narrower size distribution. Simulation experiments using Comsol software showed that at 4 °C 'droplet synthesis' of nanoparticles gets miniaturised to 'droplet-core synthesis', which is being reported for the first time. PMID:26924801

  19. Synthesis and application of bilayer-surfactant-enveloped Fe3O4 nanoparticles: water-based bilayer-surfactant-enveloped ferrofluids

    Science.gov (United States)

    Chen, Bai-yi; Qiu, Jian-hui; Feng, Hui-xia

    2016-02-01

    Superparamagnetic carbon-coated Fe3O4 nanoparticles with high magnetization (85 emu·g-1) and high crystallinity were synthesized using polyethylene glycol-4000 (PEG (4000)) as a carbon source. Fe3O4 water-based bilayer-surfactant-enveloped ferrofluids were subsequently prepared using sodium oleate and PEG (4000) as dispersants. Analyses using X-ray photoelectron spectroscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy indicate that the Fe3O4 nanoparticles with a bilayer surfactant coating retain the inverse spinel-type structure and are successfully coated with sodium oleate and PEG (4000). Transmission electron microscopy, vibrating sample magnetometry, and particle-size analysis results indicate that the coated Fe3O4 nanoparticles also retain the good saturation magnetization of Fe3O4 (79.6 emu·g-1) and that the particle size of the bilayer-surfactant-enveloped Fe3O4 nanoparticles is 42.97 nm, which is substantially smaller than that of the unmodified Fe3O4 nanoparticles (486.2 nm). UV-vis and zeta-potential analyses reveal that the ferrofluids does not agglomerate for 120 h at a concentration of 4 g·L-1, which indicates that the ferrofluids are highly stable.

  20. Synthesis, structure characterization and catalytic activity of nickel tungstate nanoparticles

    International Nuclear Information System (INIS)

    Graphical abstract: NiWO4 nanoparticles were prepared via precipitation technique. Experimental parameters of procedure were optimized statistically. Highlights: ► NiWO4 spherical nanoparticles were synthesized via direct precipitation method. ► Taguchi robust design was used for optimization of synthesis reaction parameters. ► Composition and structural properties of NiWO4 nanoparticles were characterized. ► EDAX, XRD, SEM, FT-IR, UV–vis and photoluminescence techniques were employed. ► Catalytic activity of the product in a cyclo-addition reaction was investigated. - Abstract: Taguchi robust design was applied to optimize experimental parameters for controllable, simple and fast synthesis of nickel tungstate nanoparticles. NiWO4 nanoparticles were synthesized by precipitation reaction involving addition of nickel ion solution to the tungstate aqueous reagent and then formation of nickel tungstate nucleolus which are insoluble in aqueous media. Effects of various parameters such as nickel and tungstate concentrations, flow rate of reagent addition and reactor temperature on diameter of synthesized nickel tungstate nanoparticles were investigated experimentally by the aid of orthogonal array design. The results for analysis of variance (ANOVA) showed that particle size of nickel tungstate can be effectively tuned by controlling significant variables involving nickel and tungstate concentrations and flow rate; while, temperature of the reactor has a no considerable effect on the size of NiWO4 particles. The ANOVA results proposed the optimum conditions for synthesis of nickel tungstate nanoparticles via this technique. Also, under optimum condition nanoparticles of NiWO4 were prepared and their structure and chemical composition were characterized by means of EDAX, XRD, SEM, FT-IR spectroscopy, UV–vis spectroscopy, and photoluminescence. Finally, catalytic activity of the nanoparticles in a cycloaddition reaction was examined.

  1. Synthesis, structure characterization and catalytic activity of nickel tungstate nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Pourmortazavi, Seied Mahdi, E-mail: pourmortazavi@yahoo.com [Faculty of Material and Manufacturing Technologies, Malek Ashtar University of Technology, Tehran (Iran, Islamic Republic of); Rahimi-Nasrabadi, Mehdi, E-mail: rahiminasrabadi@gmail.com [Department of Chemistry, Imam Hossein University, Tehran (Iran, Islamic Republic of); Khalilian-Shalamzari, Morteza [Department of Chemistry, Imam Hossein University, Tehran (Iran, Islamic Republic of); Zahedi, Mir Mahdi; Hajimirsadeghi, Seiedeh Somayyeh [Islamic Azad University, Varamin Pishva Branch, Varamin (Iran, Islamic Republic of); Omrani, Ismail [Department of Chemistry, Imam Hossein University, Tehran (Iran, Islamic Republic of)

    2012-12-15

    Graphical abstract: NiWO{sub 4} nanoparticles were prepared via precipitation technique. Experimental parameters of procedure were optimized statistically. Highlights: Black-Right-Pointing-Pointer NiWO{sub 4} spherical nanoparticles were synthesized via direct precipitation method. Black-Right-Pointing-Pointer Taguchi robust design was used for optimization of synthesis reaction parameters. Black-Right-Pointing-Pointer Composition and structural properties of NiWO{sub 4} nanoparticles were characterized. Black-Right-Pointing-Pointer EDAX, XRD, SEM, FT-IR, UV-vis and photoluminescence techniques were employed. Black-Right-Pointing-Pointer Catalytic activity of the product in a cyclo-addition reaction was investigated. - Abstract: Taguchi robust design was applied to optimize experimental parameters for controllable, simple and fast synthesis of nickel tungstate nanoparticles. NiWO{sub 4} nanoparticles were synthesized by precipitation reaction involving addition of nickel ion solution to the tungstate aqueous reagent and then formation of nickel tungstate nucleolus which are insoluble in aqueous media. Effects of various parameters such as nickel and tungstate concentrations, flow rate of reagent addition and reactor temperature on diameter of synthesized nickel tungstate nanoparticles were investigated experimentally by the aid of orthogonal array design. The results for analysis of variance (ANOVA) showed that particle size of nickel tungstate can be effectively tuned by controlling significant variables involving nickel and tungstate concentrations and flow rate; while, temperature of the reactor has a no considerable effect on the size of NiWO{sub 4} particles. The ANOVA results proposed the optimum conditions for synthesis of nickel tungstate nanoparticles via this technique. Also, under optimum condition nanoparticles of NiWO{sub 4} were prepared and their structure and chemical composition were characterized by means of EDAX, XRD, SEM, FT-IR spectroscopy, UV

  2. Aquatic Fern (Azolla Sp.) Assisted Synthesis of Gold Nanoparticles

    Science.gov (United States)

    Jha, Anal K.; Prasad, K.

    2016-02-01

    Aquatic pteridophyte (Azolla sp.) was taken to assess its potential to synthesize the metal (Au) nanoparticles. The synthesized particles were characterized using X-ray, UV-visible, scanning and transmission electron microscopy analyses. Nanoparticles almost spherical in shape having the sizes of 5-17nm are found. UV-visible study revealed the surface plasmon resonance at 538nm. Responsible phytochemicals for the transformation were principally phenolics, tannins, anthraquinone glycosides and sugars present abundantly in the plant thereby bestowing it adaptive prodigality. Also, the use of Azolla sp. for the synthesis of gold nanoparticles offers the benefit of eco-friendliness.

  3. Hydrothermal Synthesis of Indium Tin Oxide Nanoparticles without Chlorine Contamination

    International Nuclear Information System (INIS)

    Indium tin oxide (In2Sn1-xO5-y) nanoparticles were synthesized by hydrothermal method from stable indium tin acetylacetone complexes and post annealing at 600 .deg. C. The absence of chlorine ions shortened the synthesis process, decreased the particle agglomeration and improved the particle purity. The introduced complexing ligand acetylacetone decreased the obtained nanoparticle size. The improved powder properties accelerated the sintering of the In2Sn1-xO5-y nanoparticles and reached a relative density of 96.4% when pressureless sintered at 1400 .deg. C

  4. Vibrational properties of gold nanoparticles obtained by green synthesis

    Science.gov (United States)

    Alvarez, Ramón A. B.; Cortez-Valadez, M.; Bueno, L. Oscar Neira; Britto Hurtado, R.; Rocha-Rocha, O.; Delgado-Beleño, Y.; Martinez-Nuñez, C. E.; Serrano-Corrales, Luis Ivan; Arizpe-Chávez, H.; Flores-Acosta, M.

    2016-10-01

    This study reports the synthesis and characterization of gold nanoparticles through an ecological method to obtain nanostructures from the extract of the plant Opuntia ficus-indica. Colloidal nanoparticles show sizes that vary between 10-20 nm, and present various geometric morphologies. The samples were characterized through optical absorption, Raman Spectroscopy and Transmission Electron Microscopy (TEM). Additionally, low energy metallic clusters of Aun (n=2-20 atoms) were modeled by computational quantum chemistry. The theoretical results were obtained with Density Functional Theory (DFT). The predicted results of Au clusters show a tendency and are correlated with the experimental results concerning the optical absorption bands and Raman spectroscopy in gold nanoparticles.

  5. Sonochemical Synthesis of Silver Nanoparticles Using Starch: A Comparison

    Science.gov (United States)

    Smita, Kumari; Cumbal, Luis; Debut, Alexis; Pathak, Ravinandan Nath

    2014-01-01

    A novel approach was applied to synthesize silver nanoparticles using starch under sonication. Colloidal silver nanoparticles solution exhibited an increase of absorption from 420 to 440 nm with increase starch quantity. Transmission electron microscopy followed by selected area electron diffraction pattern analysis indicated the formation of spherical, polydispersed, amorphous, silver nanoparticles of diameter ranging from 23 to 97 nm with mean particle size of 45.6 nm. Selected area electron diffraction (SAED) confirmed partial crystalline and amorphous nature of silver nanoparticles. Silver nanoparticles synthesized in this manner can be used for synthesis of 2-aryl substituted benzimidazoles which have numerous biomedical applications. The optimized reaction conditions include 10 ml of 1 mM AgNO3, 25 mg starch, 11 pH range, and sonication for 20 min at room temperature. PMID:24587771

  6. Sonochemical Synthesis of Silver Nanoparticles Using Starch: A Comparison

    Directory of Open Access Journals (Sweden)

    Brajesh Kumar

    2014-01-01

    Full Text Available A novel approach was applied to synthesize silver nanoparticles using starch under sonication. Colloidal silver nanoparticles solution exhibited an increase of absorption from 420 to 440 nm with increase starch quantity. Transmission electron microscopy followed by selected area electron diffraction pattern analysis indicated the formation of spherical, polydispersed, amorphous, silver nanoparticles of diameter ranging from 23 to 97 nm with mean particle size of 45.6 nm. Selected area electron diffraction (SAED confirmed partial crystalline and amorphous nature of silver nanoparticles. Silver nanoparticles synthesized in this manner can be used for synthesis of 2-aryl substituted benzimidazoles which have numerous biomedical applications. The optimized reaction conditions include 10 ml of 1 mM AgNO3, 25 mg starch, 11 pH range, and sonication for 20 min at room temperature.

  7. Synthesis and Characterization of Biodegradable Lignin Nanoparticles with Tunable Surface Properties.

    Science.gov (United States)

    Richter, Alexander P; Bharti, Bhuvnesh; Armstrong, Hinton B; Brown, Joseph S; Plemmons, Dayne; Paunov, Vesselin N; Stoyanov, Simeon D; Velev, Orlin D

    2016-06-28

    Lignin nanoparticles can serve as biodegradable carriers of biocidal actives with minimal environmental footprint. Here we describe the colloidal synthesis and interfacial design of nanoparticles with tunable surface properties using two different lignin precursors, Kraft (Indulin AT) lignin and Organosolv (high-purity lignin). The green synthesis process is based on flash precipitation of dissolved lignin polymer, which enabled the formation of nanoparticles in the size range of 45-250 nm. The size evolution of the two types of lignin particles is fitted on the basis of modified diffusive growth kinetics and mass balance dependencies. The surface properties of the nanoparticles are fine-tuned by coating them with a cationic polyelectrolyte, poly(diallyldimethylammonium chloride). We analyze how the colloidal stability and dispersion properties of these two types of nanoparticles vary as a function of pH and salinities. The data show that the properties of the nanoparticles are governed by the type of lignin used and the presence of polyelectrolyte surface coating. The coating allows the control of the nanoparticles' surface charge and the extension of their stability into strongly basic regimes, facilitating their potential application at extreme pH conditions. PMID:27268077

  8. Synthesis of monodisperse MFe{sub 2}O{sub 4} (M = Fe and Zn) nanoparticles for polydiethylsiloxane-based ferrofluid with a solvothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wei [State Key Laboratory of Optoelectronic Materials and Technologies, Guangdong Provincial Key Laboratory of Photovoltaics Technologies, School of Physics and Engineering, Sun Yat-Sen University, Guangzhou 510275 (China); Laboratory of Nanophotonic Functional Materials and Devices, Institute of Optoelectronic Materials and Technology, South China Normal University, Guangzhou 510631 (China); Zhuang, Lin, E-mail: stszhl@mail.sysu.edu.cn [State Key Laboratory of Optoelectronic Materials and Technologies, Guangdong Provincial Key Laboratory of Photovoltaics Technologies, School of Physics and Engineering, Sun Yat-Sen University, Guangzhou 510275 (China); Zhang, Yong [Laboratory of Nanophotonic Functional Materials and Devices, Institute of Optoelectronic Materials and Technology, South China Normal University, Guangzhou 510631 (China); Shen, Hui [State Key Laboratory of Optoelectronic Materials and Technologies, Guangdong Provincial Key Laboratory of Photovoltaics Technologies, School of Physics and Engineering, Sun Yat-Sen University, Guangzhou 510275 (China)

    2015-09-15

    Highlights: • MFe{sub 2}O{sub 4} nanoparticles were synthesized through a facile solvothermal method. • The relationship between viscosity and temperature of the polydiethylsiloxane-based ferrofluid is discussed. • Fe{sub 3}O{sub 4} nanoparticles have a saturation magnetization of 73.06 emu/g at room temperature. - Abstract: Monodisperse MFe{sub 2}O{sub 4} (M = Fe, Zn) nanoparticles were successfully synthesized for the application of polydiethylsiloxane-based (PDES) ferrofluids (FFs) via a novel solvothermal method, with which 1-octanol and 1-octanamine act as binary solvent, oleic acid (OA) as the surfactant and metal acetylacetonate [M(acac){sub 3}](M = Fe and Zn) as the metal source. X-ray diffractometer confirms that the resultant nanoparticles are pure MFe{sub 2}O{sub 4} with a spinel structure. Infrared spectroscopy indicates that oleic acid is bound to the surface of MFe{sub 2}O{sub 4} through a covalent bond between carboxylate (COO{sup −}) and metal cations. The ratio of 1-octanol and 1-octanamine plays a key role in the formation of the sphere-shaped morphology. Transmission electron microscopy (TEM) images confirm that the Fe{sub 3}O{sub 4} particles are of 4–11 nm with good monodispersity and a narrow size distribution. The saturation magnetization of Fe{sub 3}O{sub 4} nanoparticles with sizes of 7 nm can reach up to 73.06 emu/g. Polydiethylsiloxane-based (PDES) FFs show relatively smaller changes of the viscosity with low temperatures (from −7 to 20 °C) than the polydimethylsiloxane-based (PDMS) FFs. For FFs applications, the relationship between viscosity and temperature is also discussed.

  9. Synthesis of monodisperse MFe2O4 (M = Fe and Zn) nanoparticles for polydiethylsiloxane-based ferrofluid with a solvothermal method

    International Nuclear Information System (INIS)

    Highlights: • MFe2O4 nanoparticles were synthesized through a facile solvothermal method. • The relationship between viscosity and temperature of the polydiethylsiloxane-based ferrofluid is discussed. • Fe3O4 nanoparticles have a saturation magnetization of 73.06 emu/g at room temperature. - Abstract: Monodisperse MFe2O4 (M = Fe, Zn) nanoparticles were successfully synthesized for the application of polydiethylsiloxane-based (PDES) ferrofluids (FFs) via a novel solvothermal method, with which 1-octanol and 1-octanamine act as binary solvent, oleic acid (OA) as the surfactant and metal acetylacetonate [M(acac)3](M = Fe and Zn) as the metal source. X-ray diffractometer confirms that the resultant nanoparticles are pure MFe2O4 with a spinel structure. Infrared spectroscopy indicates that oleic acid is bound to the surface of MFe2O4 through a covalent bond between carboxylate (COO−) and metal cations. The ratio of 1-octanol and 1-octanamine plays a key role in the formation of the sphere-shaped morphology. Transmission electron microscopy (TEM) images confirm that the Fe3O4 particles are of 4–11 nm with good monodispersity and a narrow size distribution. The saturation magnetization of Fe3O4 nanoparticles with sizes of 7 nm can reach up to 73.06 emu/g. Polydiethylsiloxane-based (PDES) FFs show relatively smaller changes of the viscosity with low temperatures (from −7 to 20 °C) than the polydimethylsiloxane-based (PDMS) FFs. For FFs applications, the relationship between viscosity and temperature is also discussed

  10. Hydrogel nanoparticle based immunoassay

    Energy Technology Data Exchange (ETDEWEB)

    Liotta, Lance A; Luchini, Alessandra; Petricoin, Emanuel F; Espina, Virginia

    2015-04-21

    An immunoassay device incorporating porous polymeric capture nanoparticles within either the sample collection vessel or pre-impregnated into a porous substratum within fluid flow path of the analytical device is presented. This incorporation of capture particles within the immunoassay device improves sensitivity while removing the requirement for pre-processing of samples prior to loading the immunoassay device. A preferred embodiment is coreshell bait containing capture nanoparticles which perform three functions in one step, in solution: a) molecular size sieving, b) target analyte sequestration and concentration, and c) protection from degradation. The polymeric matrix of the capture particles may be made of co-polymeric materials having a structural monomer and an affinity monomer, the affinity monomer having properties that attract the analyte to the capture particle. This device is useful for point of care diagnostic assays for biomedical applications and as field deployable assays for environmental, pathogen and chemical or biological threat identification.

  11. Green Synthesis of Metallic Nanoparticles via Biological Entities

    Directory of Open Access Journals (Sweden)

    Monaliben Shah

    2015-10-01

    Full Text Available Nanotechnology is the creation, manipulation and use of materials at the nanometre size scale (1 to 100 nm. At this size scale there are significant differences in many material properties that are normally not seen in the same materials at larger scales. Although nanoscale materials can be produced using a variety of traditional physical and chemical processes, it is now possible to biologically synthesize materials via environment-friendly green chemistry based techniques. In recent years, the convergence between nanotechnology and biology has created the new field of nanobiotechnology that incorporates the use of biological entities such as actinomycetes algae, bacteria, fungi, viruses, yeasts, and plants in a number of biochemical and biophysical processes. The biological synthesis via nanobiotechnology processes have a significant potential to boost nanoparticles production without the use of harsh, toxic, and expensive chemicals commonly used in conventional physical and chemical processes. The aim of this review is to provide an overview of recent trends in synthesizing nanoparticles via biological entities and their potential applications.

  12. Facile synthesis of self-stabilized polyphenol nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bilici, Ali, E-mail: alibilici66@hotmail.com [Lapseki Vocational School, Çanakkale Onsekiz Mart University, Lapseki, Çanakkale 17020 (Turkey); Department of Chemistry, Polymer Synthesis and Analysis Laboratory, Faculty of Science and Arts, Çanakkale Onsekiz Mart University, Çanakkale 17020 (Turkey); Doğan, Fatih, E-mail: fatihdogan@comu.edu.tr [Secondary Science and Mathematics Education, Faculty of Education, Canakkale Onsekiz Mart University, Canakkale 17100 (Turkey); Department of Chemistry, Polymer Synthesis and Analysis Laboratory, Faculty of Science and Arts, Çanakkale Onsekiz Mart University, Çanakkale 17020 (Turkey); Yıldırım, Mehmet [Department of Materials Science and Engineering, Faculty of Engineering, Çanakkale Onsekiz Mart University, Çanakkale 17020 (Turkey); Department of Chemistry, Polymer Synthesis and Analysis Laboratory, Faculty of Science and Arts, Çanakkale Onsekiz Mart University, Çanakkale 17020 (Turkey); Kaya, İsmet [Department of Chemistry, Polymer Synthesis and Analysis Laboratory, Faculty of Science and Arts, Çanakkale Onsekiz Mart University, Çanakkale 17020 (Turkey)

    2013-06-15

    We describe here the facile synthesis (in two-steps) of green light emitting phenol polymer with an azomethine side group. For this purpose, hydroxy functionalized-Schiff base monomer, HPMBT, was obtained by condensation of 2,3,4-trihydroxybenzaldehyde with 2-aminophenol. Subsequent oxidation of the monomer in alkaline medium by NaOCl yielded to corresponding phenol polymer (PHPMBT) with molecular weight ca. 34,500 Da. The characterizations were performed by NMR, FT-IR, UV–vis, gel permeation chromatography (GPC), thermogravimetry (TG), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), cyclic voltammetry (CV), photoluminescence (PL), dynamic light scattering (DLS) and scanning electron microscope (SEM) analysis. PL analysis indicated that HPMBT was non-fluorescent whereas PHPMBT was a green light emitter. In addition, the redox behaviors of the polymer were explored by cyclic voltammetry (CV), assigned it's electroactive nature. The formation of nano-sized polyphenol particles was revealed by the SEM and DLS analyses. A possible mechanism for the formation and self-stabilization of the polyphenol nanoparticles was also suggested. - Highlights: • The nano-sized polyphenol particles were facilely obtained by a template-free oxidative polymerization process. • A possible mechanism for the formation and self-stabilization of the nanoparticles was proposed. • These electroactive particles emitted green light, efficiently. • The obtained polymer was well soluble in polar organic solvents.

  13. Solid-phase synthesis of molecularly imprinted nanoparticles.

    Science.gov (United States)

    Canfarotta, Francesco; Poma, Alessandro; Guerreiro, Antonio; Piletsky, Sergey

    2016-03-01

    Molecularly imprinted polymers (MIPs) are synthetic materials, generally based on acrylic or methacrylic monomers, that are polymerized in the presence of a specific target molecule called the 'template' and capable of rebinding selectively to this target molecule. They have the potential to be low-cost and robust alternatives to biomolecules such as antibodies and receptors. When prepared by traditional synthetic methods (i.e., with free template in solution), their usefulness has been limited by high binding site heterogeneity, the presence of residual template and the fact that the production methods are complex and difficult to standardize. To overcome some of these limitations, we developed a method for the synthesis of MIP nanoparticles (nanoMIPs) using an innovative solid-phase approach, which relies on the covalent immobilization of the template molecules onto the surface of a solid support (glass beads). The obtained nanoMIPs are virtually free of template and demonstrate high affinity for the target molecule (e.g., melamine and trypsin in our published work). Because of an affinity separation step performed on the solid phase after polymerization, poor binders and unproductive polymer are removed, so the final product has more uniform binding characteristics. The overall protocol, starting from the immobilization of the template onto the solid phase and including the purification and characterization of the nanoparticles, takes up to 1 week.

  14. Synthesis of Gold Nanoparticles Using Whole Cells of Geotrichum candidum

    Directory of Open Access Journals (Sweden)

    Amit Kumar Mittal

    2013-01-01

    Full Text Available The synthesis of nanoparticles with desired size and shape is an important area of research in nanotechnology. Use of biological system is an alternative approach to chemical and physical procedures for the synthesis of metal nanoparticles. An efficient environment-friendly approach for the biosynthesis of rapid and stable Gold nanoparticles (AuNPs using whole cells of Geotrichum candidum is discussed in this paper. The enzymes/proteins present in the microorganism might be responsible for the reduction of metal salts to nanoparticles. Various reaction parameters such as culture age, temperature, pH, metal salt, and cell mass concentrations were optimized. The AuNPs were characterized by UV-visible spectroscopy, dynamic light scattering (DLS, energy dispersive spectroscopy (EDS, scanning electron microscope (SEM, and Fourier transform infrared spectroscopy (FTIR. Nanoparticles were isolated by sonicating the whole cells after treatment with Tween 80. The whole cell mediated process showed the simplistic, feasible, easy to scale up, and low-cost approach for the synthesis of AuNPs.

  15. Biogenic synthesis of silver nanoparticles using guava (Psidium guajava) leaf extract and its antibacterial activity against Pseudomonas aeruginosa

    Science.gov (United States)

    Bose, Debadin; Chatterjee, Someswar

    2015-09-01

    Among the various inorganic nanoparticles, silver nanoparticles have received substantial attention in the field of antimicrobial research. For safe and biocompatible use of silver nanoparticles in antimicrobial research, the different biogenic routes are developed to synthesize silver nanoparticles that do not use toxic chemicals. Among those, to synthesize silver nanoparticles, the use of plant part extract becomes an emerging field because plant part acts as reducing as well as capping agent. For large-scale production of antibacterial silver nanoparticles using plant part, the synthesis route should be very simple, rapid, cost-effective and environment friendly based on easy availability and non-toxic nature of plant, stability and antibacterial potential of biosynthesized nanoparticles. In the present study, we report a very simple, rapid, cost-effective and environment friendly route for green synthesis of silver nanoparticles using guava (Psidium guajava) leaf extract as reducing as well as capping agent. This plant has been opted for the present study for its known medicinal properties, and it is easily available in all seasons and everywhere. The biosynthesized silver nanoparticles are characterized by UV-Vis and TEM analysis. The average particle size is 40 nm in the range of 10-90 nm. The antibacterial activity of these nanoparticles against Pseudomonas aeruginosa MTCC 741 has been measured by disc diffusion method, agar cup assay and serial dilution turbidity measurement assay. The results show that green synthesized silver nanoparticles, using guava (Psidium guajava) leaf extract, have a potential to inhibit the growth of bacteria.

  16. Biogenic synthesis of silver nanoparticles using guava ( Psidium guajava) leaf extract and its antibacterial activity against Pseudomonas aeruginosa

    Science.gov (United States)

    Bose, Debadin; Chatterjee, Someswar

    2016-08-01

    Among the various inorganic nanoparticles, silver nanoparticles have received substantial attention in the field of antimicrobial research. For safe and biocompatible use of silver nanoparticles in antimicrobial research, the different biogenic routes are developed to synthesize silver nanoparticles that do not use toxic chemicals. Among those, to synthesize silver nanoparticles, the use of plant part extract becomes an emerging field because plant part acts as reducing as well as capping agent. For large-scale production of antibacterial silver nanoparticles using plant part, the synthesis route should be very simple, rapid, cost-effective and environment friendly based on easy availability and non-toxic nature of plant, stability and antibacterial potential of biosynthesized nanoparticles. In the present study, we report a very simple, rapid, cost-effective and environment friendly route for green synthesis of silver nanoparticles using guava ( Psidium guajava) leaf extract as reducing as well as capping agent. This plant has been opted for the present study for its known medicinal properties, and it is easily available in all seasons and everywhere. The biosynthesized silver nanoparticles are characterized by UV-Vis and TEM analysis. The average particle size is 40 nm in the range of 10-90 nm. The antibacterial activity of these nanoparticles against Pseudomonas aeruginosa MTCC 741 has been measured by disc diffusion method, agar cup assay and serial dilution turbidity measurement assay. The results show that green synthesized silver nanoparticles, using guava ( Psidium guajava) leaf extract, have a potential to inhibit the growth of bacteria.

  17. Synthesis of powdered silver nanoparticles using hydrogen in aqueous medium

    Institute of Scientific and Technical Information of China (English)

    Kushal D.Bhatte; Krishna M.Deshmukh; Yogesh P.Patil; Dinesh N.Sawant; Shin-Ichiro Fujita; Masahiko Arai; Bhalchandra M.Bhanage

    2012-01-01

    Environmentally benign one-pot protocol is used in the synthesis of silver nanoparticles (AgNPs) in powder form,involving the reduction of silver nitrate in the presence of fully hydrolyzed polyvinyl alcohol (PVA) as stabilizer by hydrogen (H2) as reducing agent in aqueous medium.Fully hydrolyzed biodegradable PVA has extremely low cytotoxicity,making it a favorable stabilizer from green perspective.In the present methodology,essentially naked silver nanoparticles are obtained in good yield.The prepared silver nanoparticles were characterized by TEM,XRD,EDAX,UV-Vis spectroscopy and DLS histogram,and studied for its activity as a recvclable catalyst for synthesis of different enaminones.

  18. Synthesis of silver nanoparticles in melts of amphiphilic polyesters

    International Nuclear Information System (INIS)

    The current work presents a one-step procedure for the synthesis of amphiphilic silver nanoparticles suitable for production of silver-filled polymeric materials. This solvent free synthesis via reduction of Tollens’ reagent as silver precursor in melts of amphiphilic polyesters consisting of hydrophilic poly(ethylene glycol) blocks and hydrophobic alkyl chains allows the production of silver nanoparticles without any by-product formation. This makes them especially interesting for the production of medical devices with antimicrobial properties. In this article the influences of the chain length of the hydrophobic block in the amphiphilic polyesters and the process temperature on the particle size distribution (PSD) and the stability of the particles against agglomeration are discussed. According to the results of spectroscopic and viscosimetric investigations the silver precursor is reduced to elemental silver nanoparticles by a single electron transfer process from the poly(ethylene glycol) chain to the silver ion. (paper)

  19. Microwave-hydrothermal synthesis of barium strontium titanate nanoparticles

    International Nuclear Information System (INIS)

    Research highlights: → Barium strontium titanate nanoparticles were obtained by the Hydrothemal microwave technique (HTMW) → This is a genuine technique to obtain nanoparticles at low temperature and short times → Barium strontium titanate free of carbonates with tetragonal structure was grown at 130 oC. - Abstract: Hydrothermal-microwave method (HTMW) was used to synthesize crystalline barium strontium titanate (Ba0.8Sr0.2TiO3) nanoparticles (BST) in the temperature range of 100-130 oC. The crystallization of BST with tetragonal structure was reached at all the synthesis temperatures along with the formation of BaCO3 as a minor impurity at lower syntheses temperatures. Typical FT-IR spectra for tetragonal (BST) nanoparticles presented well defined bands, indicating a substantial short-range order in the system. TG-DTA analyses confirmed the presence of lattice OH- groups, commonly found in materials obtained by HTMW process. FE/SEM revealed that lower syntheses temperatures led to a morphology that consisted of uniform grains while higher syntheses temperature consisted of big grains isolated and embedded in a matrix of small grains. TEM has shown BST nanoparticles with diameters between 40 and 80 nm. These results show that the HTMW synthesis route is rapid, cost effective, and could serve as an alternative to obtain BST nanoparticles.

  20. Synthesis, structure characterization and catalytic activity of nickel tungstate nanoparticles

    Science.gov (United States)

    Pourmortazavi, Seied Mahdi; Rahimi-Nasrabadi, Mehdi; Khalilian-Shalamzari, Morteza; Zahedi, Mir Mahdi; Hajimirsadeghi, Seiedeh Somayyeh; Omrani, Ismail

    2012-12-01

    Taguchi robust design was applied to optimize experimental parameters for controllable, simple and fast synthesis of nickel tungstate nanoparticles. NiWO4 nanoparticles were synthesized by precipitation reaction involving addition of nickel ion solution to the tungstate aqueous reagent and then formation of nickel tungstate nucleolus which are insoluble in aqueous media. Effects of various parameters such as nickel and tungstate concentrations, flow rate of reagent addition and reactor temperature on diameter of synthesized nickel tungstate nanoparticles were investigated experimentally by the aid of orthogonal array design. The results for analysis of variance (ANOVA) showed that particle size of nickel tungstate can be effectively tuned by controlling significant variables involving nickel and tungstate concentrations and flow rate; while, temperature of the reactor has a no considerable effect on the size of NiWO4 particles. The ANOVA results proposed the optimum conditions for synthesis of nickel tungstate nanoparticles via this technique. Also, under optimum condition nanoparticles of NiWO4 were prepared and their structure and chemical composition were characterized by means of EDAX, XRD, SEM, FT-IR spectroscopy, UV-vis spectroscopy, and photoluminescence. Finally, catalytic activity of the nanoparticles in a cycloaddition reaction was examined.

  1. Synthesis of supported bimetallic nanoparticles with controlled size and composition distributions for active site elucidation

    Energy Technology Data Exchange (ETDEWEB)

    Hakim, Sikander H.; Sener, Canan; Alba Rubio, Ana C.; Gostanian, Thomas M.; O' neill, Brandon J; Ribeiro, Fabio H.; Miller, Jeffrey T.; Dumesic, James A

    2015-08-01

    Elucidation of active sites in supported bimetallic catalysts is complicated by the high level of dispersity in the nanoparticle size and composition that is inherent in conventional methods of catalyst preparation. We present a synthesis strategy that leads to highly dispersed, bimetallic nanoparticles with uniform particle size and composition by means of controlled surface reactions. We demonstrate the synthesis of three systems, RhMo, PtMo, and RhRe, consisting of a highly reducible metal with an oxophilic promoter. These catalysts are characterized by FTIR, CO chemisorption, STEM/EDS, TPR, and XAS analysis. The catalytic properties of these bimetallic nanoparticles were probed for the selective CO hydrogenolysis of (hydroxymethyl)tetrahydropyran to produce 1,6 hexanediol. Based on the characterization results and reactivity trends, the active sites in the hydrogenolysis reaction are identified to be small ensembles of the more noble metal (Rh, Pt) adjacent to highly reduced moieties of the more oxophilic metal (Mo, Re).

  2. Recent Advances in the Synthesis and Stabilization of Nickel and Nickel Oxide Nanoparticles: A Green Adeptness

    Science.gov (United States)

    Rani, Aneela

    2016-01-01

    Green protocols for the synthesis of nanoparticles have been attracting a lot of attention because they are eco-friendly, rapid, and cost-effective. Nickel and nickel oxide nanoparticles have been synthesized by green routes and characterized for impact of green chemistry on the properties and biological effects of nanoparticles in the last five years. Green synthesis, properties, and applications of nickel and nickel oxide nanoparticles have been reported in the literature. This review summarizes the synthesis of nickel and nickel oxide nanoparticles using different biological systems. This review also provides comparative overview of influence of chemical synthesis and green synthesis on structural properties of nickel and nickel oxide nanoparticles and their biological behavior. It concludes that green methods for synthesis of nickel and nickel oxide nanoparticles are better than chemical synthetic methods. PMID:27413375

  3. New approach for direct chemical synthesis of hexagonal Co nanoparticles

    Science.gov (United States)

    Abel, Frank M.; Tzitzios, Vasilis; Hadjipanayis, George C.

    2016-02-01

    In this paper, we explore the possibility of producing hexagonal Cobalt nanoparticles, with high saturation magnetization by direct chemical synthesis. The nanoparticles were synthesized by reduction of anhydrous cobalt (II) chloride by NaBH4 in tetraglyme at temperatures in the range of 200-270 °C under a nitrogen-hydrogen atmosphere. The reactions were done at high temperatures to allow for the formation of as-made hexagonal cobalt. The size of the particles was controlled by the addition of different surfactants. The best magnetic properties so far were obtained on spherical hexagonal Co nanoparticles with an average size of 45 nm, a saturation magnetization of 143 emu/g and coercivity of 500 Oe. the saturation magnetization and coercivity were further improved by annealing the Co nanoparticles leading to saturation magnetization of 160 emu/g and coercivity of 540 Oe.

  4. Solution synthesis of metal silicide nanoparticles.

    Science.gov (United States)

    McEnaney, Joshua M; Schaak, Raymond E

    2015-02-01

    Transition-metal silicides are part of an important family of intermetallic compounds, but the high-temperature reactions that are generally required to synthesize them preclude the formation of colloidal nanoparticles. Here, we show that palladium, copper, and nickel nanoparticles react with monophenylsilane in trioctylamine and squalane at 375 °C to form colloidal Pd(2)Si, Cu(3)Si, and Ni(2)Si nanoparticles, respectively. These metal silicide nanoparticles were screened as electrocatalysts for the hydrogen evolution reaction, and Pd(2)Si and Ni(2)Si were identified as active catalysts that require overpotentials of -192 and -243 mV, respectively, to produce cathodic current densities of -10 mA cm(-2).

  5. Synthesis and Properties of Magnetic Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Sixin LI; Jiancheng ZHANG; Yue SHEN; Bo NI; Jingang ZHANG

    2006-01-01

    The uniform mesoporous SBA-15 consisting of SiO2 with long-range channels offers an excellent host material to synthesize or assemble the magnetic nanocomposites, such as Fe, Ni.In this paper, highly dispersed and uniform iron nanoparticles were incorporated into the pore channels of SBA-15 through a newly developed strategy in which some kinds of coupling agents were used to entrap the nanoparticles into the silica framework.The X-ray diffraction(XRD), fourier transmission infrared spectroscopy(FTIR), high-resolution transmission electronic microscopy(HRTEM)and energy dispersive X-ray spectroscopy(EDX)were performed to further identify the successful incorporation and grafting of iron. Compared with other ordinary non-assembled magnetic nanoparticles, the assembled Fe nanoparticles with the diameter even in the size range of 5~6 nm still have better magnetic properties.

  6. Synthesis of superparamagnetic particles with tunable morphologies: the role of nanoparticle-nanoparticle interactions.

    Science.gov (United States)

    O'Mahony, James J; Platt, Mark; Kilinc, Devrim; Lee, Gil

    2013-02-26

    Superparamagnetic microparticles are extensively used in the purification of biomolecules due to the speed and ease of magnetic separation. It is desirable that the microparticles used in biological affinity separations have both high surface area and high magnetic mobility to facilitate a high binding capacity of target biomolecules and their rapid removal from solution, respectively. Scaling laws for conventional spherical superparamagnetic microparticles are such that increasing the microparticle specific surface area results in a significant decrease in the magnetic mobility. More favorable combinations of these key parameters can be found if alternative microparticle morphologies are developed for use in affinity separations. Emulsion-templated self-assembly of iron oxide nanoparticles into microparticles using oil-in-water emulsions was carried out using a modified Couette shear mixer with separate inlet ports for the oil and aqueous phases, enabling high throughput microparticle synthesis. By controlling the dissolved nanoparticle concentration and nanoparticle surface activity at the droplet interfaces, the resulting microparticles were tuned to spherical, dimpled, or crumpled morphologies. The specific binding capacity and magnetic mobility of each type of microparticle were measured by a peroxidase-based colorimetric assay and by their magnetic field-induced motion in a viscous fluid, respectively. Superparamagnetic microparticles with dimpled and crumpled morphologies were found to have higher specific binding capacities compared to spherical microparticles, while maintaining high magnetic field velocities due to their high iron oxide content. Superparamagnetic microparticles with these novel morphologies would make excellent tools for affinity-based bioseparations where binding capacity and magnetic mobility are key factors. PMID:23373513

  7. Synthesis and characterization of new fluorescent nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Liang Tao; Xu Hun; Zhu Jun Zhang

    2008-01-01

    A novel kind of fluorescent nanoparticles (FNPs) has been prepared using a precipitation polymerization method.Methacrylic acid,trimethylolpropane trimethacrylate and azobisisobutyronitrile were used as functional-monomer,cross-linker and initiator,respectively.Compared with other fluorescent nanoparticles,the FNPs have the characteristics including low dye leakage and good photostability.The fluorescence microscopy imaging indicates that the FNPs can be used as fluorescent labels in bioanalysis.

  8. Synthesis and optical properties of silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Jaiveer [Department of Physics, ISLE, IPS Academy, Rajendra Nagar, Indore 452012, MP (India); Kaurav, Netram, E-mail: netramkaurav@yahoo.co.uk [Department of Physics, Holkar Science College, A-B Road, Indore 452001 (India); Choudhary, K. K. [Department of Physics, National Defence Academy, Khadakwasala, Pune -411023 (India); Okram, Gunadhor S. [Electrical Transport Laboratory, UGC-DAR Consortium for Scientific Research, University Campus, Khandwa Road, Indore-452001 (India)

    2015-07-31

    The preparation of stable, uniform silver nanoparticles by reduction of silver acetate by ethylene glycol (EG) is reported in the present paper. It is a simple process of recent interest for obtaining silver nanoparticles. The samples were characterized by X-Ray diffraction (XRD), which reveals an average particle size (D) of 38 nm. The UV/Vis spectra show that an absorption peak, occurring due to surface plasmon resonance (SPR), exists at 319 nm.

  9. Spatially and size selective synthesis of Fe-based nanoparticles on ordered mesoporous supports as highly active and stable catalysts for ammonia decomposition.

    Science.gov (United States)

    Lu, An-Hui; Nitz, Joerg-Joachim; Comotti, Massimiliano; Weidenthaler, Claudia; Schlichte, Klaus; Lehmann, Christian W; Terasaki, Osamu; Schüth, Ferdi

    2010-10-13

    Uniform and highly dispersed γ-Fe(2)O(3) nanoparticles with a diameter of ∼6 nm supported on CMK-5 carbons and C/SBA-15 composites were prepared via simple impregnation and thermal treatment. The nanostructures of these materials were characterized by XRD, Mössbauer spectroscopy, XPS, SEM, TEM, and nitrogen sorption. Due to the confinement effect of the mesoporous ordered matrices, γ-Fe(2)O(3) nanoparticles were fully immobilized within the channels of the supports. Even at high Fe-loadings (up to about 12 wt %) on CMK-5 carbon no iron species were detected on the external surface of the carbon support by XPS analysis and electron microscopy. Fe(2)O(3)/CMK-5 showed the highest ammonia decomposition activity of all previously described Fe-based catalysts in this reaction. Complete ammonia decomposition was achieved at 700 °C and space velocities as high as 60,000 cm(3) g(cat)(-1) h(-1). At a space velocity of 7500 cm(3) g(cat)(-1) h(-1), complete ammonia conversion was maintained at 600 °C for 20 h. After the reaction, the immobilized γ-Fe(2)O(3) nanoparticles were found to be converted to much smaller nanoparticles (γ-Fe(2)O(3) and a small fraction of nitride), which were still embedded within the carbon matrix. The Fe(2)O(3)/CMK-5 catalyst is much more active than the benchmark NiO/Al(2)O(3) catalyst at high space velocity, due to its highly developed mesoporosity. γ-Fe(2)O(3) nanoparticles supported on carbon-silica composites are structurally much more stable over extended periods of time but less active than those supported on carbon. TEM observation reveals that iron-based nanoparticles penetrate through the carbon layer and then are anchored on the silica walls, thus preventing them from moving and sintering. In this way, the stability of the carbon-silica catalyst is improved. Comparison with the silica supported iron oxide catalyst reveals that the presence of a thin layer of carbon is essential for increased catalytic activity. PMID:20849104

  10. Solid state synthesis of starch-capped silver nanoparticles.

    Science.gov (United States)

    Hebeish, A; Shaheen, Th I; El-Naggar, Mehrez E

    2016-06-01

    The present research addresses the establishment of a technique which is solely devoted to environmentally friendly one-pot green synthesis of dry highly stable powdered silver nanoparticles (AgNPs) using starch as both reductant and stabilizing agent in the presence of sodium hydroxide. It is believed that the sodium hydroxide can improve the reduction potential of starch. Thus when the alkali treated starch is submitted to addition of silver nitrate (AgNO3), the alkali treated starch induces the well-established dual role of starch; reduction of silver ions (Ag(+)) to AgNPs and capping the as-formed AgNPs to prevent them from further growth and agglomeration. Beside assessment of AgNPs formation, structural and morphological characteristics of AgNPs are investigated by making use of UV-vis spectroscopy, transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential, FT-IR and X-ray diffraction (XRD) analysis. Research outputs signify (a) the absorbance around 410-420nm in the UV-vis spectra of AgNPs appears most, probably owing to the presence of nanosized silver particles and the intensity of this peak increases by increasing AgNO3 concentration; (b) that highly stable AgNPs with well-dispersed particle are successfully prepared using the present research-based innovation; (c) that the size of AgNPs does not exceed 30nm with sphere-like morphology even at the highest Ag(+) concentration employed during synthesis operation; (d) that the XRD and FT-IR confirm the successful preparation of pure AgNPs without noticeable impurities; (d) and that the one-pot synthesis of powdered AgNPs in large scale is clean and easily operated and easily transportation which may be applied as per demands of industries such as textile and painting industry. PMID:26902893

  11. Green and Rapid Synthesis of Anticancerous Silver Nanoparticles by Saccharomyces boulardii and Insight into Mechanism of Nanoparticle Synthesis

    Directory of Open Access Journals (Sweden)

    Abhishek Kaler

    2013-01-01

    Full Text Available Rapidly developing field of nanobiotechnology dealing with metallic nanoparticle (MNP synthesis is primarily lacking control over size, shape, dispersity, yield, and reaction time. Present work describes an ecofriendly method for the synthesis of silver nanoparticles (AgNPs by cell free extract (CFE of Saccharomyces boulardii. Parameters such as culture age (stationary phase growth, cell mass concentration (400 mg/mL, temperature (35°C, and reaction time (4 h, have been optimized to exercise a control over the yield of nanoparticles and their properties. Nanoparticle (NP formation was confirmed by UV-Vis spectroscopy, elemental composition by EDX (energy dispersive X-rays analysis, and size and shape by transmission electron microscopy. Synthesized nanoparticles had the size range of 3–10 nm with high negative zeta potential (−31 mV indicating excellent stability. Role of proteins/peptides in NP formation and their stability were also elucidated. Finally, anticancer activity of silver nanoparticles as compared to silver ions was determined on breast cancer cell lines.

  12. Gold nanoparticle (AuNPs) and gold nanopore (AuNPore) catalysts in organic synthesis.

    Science.gov (United States)

    Takale, Balaram S; Bao, Ming; Yamamoto, Yoshinori

    2014-04-01

    Organic synthesis using gold has gained tremendous attention in last few years, especially heterogeneous gold catalysis based on gold nanoparticles has made its place in almost all organic reactions, because of the robust and green nature of gold catalysts. In this context, gold nanopore (AuNPore) with a 3D metal framework is giving a new dimension to heterogeneous gold catalysts. Interestingly, AuNPore chemistry is proving better than gold nanoparticles based chemistry. In this review, along with recent advances, major discoveries in heterogeneous gold catalysis are discussed.

  13. Study of mechanism of enhanced antibacterial activity by green synthesis of silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Parashar, Upendra Kumar; Srivastava, Sunil K; Srivastava, Anchal [Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Kumar, Vinod; Saxena, Preeti S [Department of Zoology, Banaras Hindu University, Varanasi 22005 (India); Bera, Tanmay [Department of Mechanical, Materials and Aerospace Engineering, University of Central Florida, Orlando, FL 32816 (United States); Nath, Gopal [Department of Microbiology, Institute of Medical Science, Banaras Hindu University, Varanasi 22005 (India); Giri, Rajiv, E-mail: anchalbhu@gmail.com [Department of Materials Science and Engineering, Norwegian University of Science and Technology, NO-7491 Trondheim (Norway)

    2011-10-14

    The extensive use of silver nanoparticles needs a synthesis process that is greener without compromising their properties. The present study describes a novel green synthesis of silver nanoparticles using Guava (Psidium guajava) leaf extract. In order to compare with the conventionally synthesized ones, we also prepared Ag-NPs by chemical reduction. Their optical and morphological characteristics were thoroughly investigated and tested for their antibacterial properties on Escherichia coli. The green synthesized silver nanoparticles showed better antibacterial properties than their chemical counterparts even though there was not much difference between their morphologies. Fourier transform infrared (FTIR) spectroscopic analysis of the used extract and as-synthesized silver nanoparticles suggests the possible reduction of Ag{sup +} by the water-soluble ingredients of the guava leaf like tannins, eugenol and flavonoids. The possible reaction mechanism for the reduction of Ag{sup +} has been proposed and discussed. The time-dependent electron micrographs and the simulation studies indicated that a physical interaction between the silver nanoparticles and the bacterial cell membrane may be responsible for this effect. Based on the findings, it seems very reasonable to believe that this greener way of synthesizing silver nanoparticles is not just an environmentally viable technique but it also opens up scope to improve their antibacterial properties.

  14. Polymer/Iron Oxide Nanoparticle Composites—A Straight Forward and Scalable Synthesis Approach

    Directory of Open Access Journals (Sweden)

    Jens Sommertune

    2015-08-01

    Full Text Available Magnetic nanoparticle systems can be divided into single-core nanoparticles (with only one magnetic core per particle and magnetic multi-core nanoparticles (with several magnetic cores per particle. Here, we report multi-core nanoparticle synthesis based on a controlled precipitation process within a well-defined oil in water emulsion to trap the superparamagnetic iron oxide nanoparticles (SPION in a range of polymer matrices of choice, such as poly(styrene, poly(lactid acid, poly(methyl methacrylate, and poly(caprolactone. Multi-core particles were obtained within the Z-average size range of 130 to 340 nm. With the aim to combine the fast room temperature magnetic relaxation of small individual cores with high magnetization of the ensemble of SPIONs, we used small (<10 nm core nanoparticles. The performed synthesis is highly flexible with respect to the choice of polymer and SPION loading and gives rise to multi-core particles with interesting magnetic properties and magnetic resonance imaging (MRI contrast efficacy.

  15. Polymer/Iron Oxide Nanoparticle Composites--A Straight Forward and Scalable Synthesis Approach.

    Science.gov (United States)

    Sommertune, Jens; Sugunan, Abhilash; Ahniyaz, Anwar; Bejhed, Rebecca Stjernberg; Sarwe, Anna; Johansson, Christer; Balceris, Christoph; Ludwig, Frank; Posth, Oliver; Fornara, Andrea

    2015-01-01

    Magnetic nanoparticle systems can be divided into single-core nanoparticles (with only one magnetic core per particle) and magnetic multi-core nanoparticles (with several magnetic cores per particle). Here, we report multi-core nanoparticle synthesis based on a controlled precipitation process within a well-defined oil in water emulsion to trap the superparamagnetic iron oxide nanoparticles (SPION) in a range of polymer matrices of choice, such as poly(styrene), poly(lactid acid), poly(methyl methacrylate), and poly(caprolactone). Multi-core particles were obtained within the Z-average size range of 130 to 340 nm. With the aim to combine the fast room temperature magnetic relaxation of small individual cores with high magnetization of the ensemble of SPIONs, we used small (<10 nm) core nanoparticles. The performed synthesis is highly flexible with respect to the choice of polymer and SPION loading and gives rise to multi-core particles with interesting magnetic properties and magnetic resonance imaging (MRI) contrast efficacy. PMID:26307966

  16. Synthesis of oxime-based CO-releasing molecules, CORMs and their immobilization on maghemite nanoparticles for magnetic-field induced CO release.

    Science.gov (United States)

    Meyer, Hajo; Brenner, Markus; Höfert, Simon-P; Knedel, Tim-O; Kunz, Peter C; Schmidt, Annette M; Hamacher, Alexandra; Kassack, Matthias U; Janiak, Christoph

    2016-05-01

    Oxime-based CO-releasing molecules (oximeCORMs) were immobilized with a catechol-modified backbone on maghemite iron oxide nanoparticles (IONPs) to give oximeCORM@IONP. The CO release from the free and immobilized oximeCORMs was measured using the standard myoglobin assay. The oximeCORM-nanoparticles were coated with dextran for improved water solubility and confined into an alginate shell for protection and separation from the surrounding myoglobin assay to allow for CO release studies by UV/Vis absorption without interference from highly-absorptive oximeCORM@IONP. Half-lifes of the oxime-based polymer-confined alginate@dextran@oximeCORM@IONPs were estimated at 20 °C to 814 ± 23 min, at 37 °C to 346 ± 83 min and at 50 °C to 73 ± 1 min. The alginate@dextran@oximeCORM@IONP composite showed a further decrease of the half-life of CO release to 153 ± 27 min at 37 °C through local magnetic heating of the susceptible iron oxide nanoparticles with application of an external alternating magnetic field (31.7 kA m(-1), 247 kHz, 39.9 mTesla). The activation energy for the CO release from molecular dicarbonylchlorido(imidazole-2-carbaldehydeoxime)(alkoxycarbonyl)ruthenium(ii) complexes is determined to be ∼100 kJ mol(-1) for five different imidazole-oxime derivatives. PMID:27048982

  17. Rapid Synthesis of Size-controlled Gold Nanoparticles by Complex Intramolecular Photoreduction

    Institute of Scientific and Technical Information of China (English)

    DONG Shou-an; YANG Sheng-chun; TANG Chun

    2007-01-01

    A rapid synthesis of size-controlled gold nanoparticles was proposed. The method is based on the sensitive intramolecular photoreduction reaction of Fe( Ⅲ )-EDTA complex in chloroacetic acid-sodium acetate buffer solution,where Fe(Ⅱ)-EDTA complex generated by photo-promotion acts as a reductant of AuCl4- ions. Gold nanoparticles formed were stabilized by EDTA ligand or other protective agents added. As a result, well-dispersed gold nanoparticles with an average diameter range of 6.7 to 50. 9 nm were obtained. According to the characterizations by the UV spectrum and TEM, the intramolecular charge transfer of the excited states of complex Fe(Ⅲ) -EDTA and the mechanism of forming gold nanoparticles were discussed in detail.

  18. Eco-Friendly Synthesis of Fucoidan-Stabilized Gold Nanoparticles

    Directory of Open Access Journals (Sweden)

    Kriengsak Lirdprapamongkol

    2010-01-01

    Full Text Available Problem statement: Metallic gold nanoparticles (AuNPs are widely used in many applications including medical, pharmaceutical, diagnostics and sensors. The chemical synthesis of AuNPs normally requires synthetic materials which might cause the toxicological concerns. The use of naturally occurring materials like fucoidans for successful synthesis of AuNPs is of interests. Approach: Fucoidans as sulfated polysaccharides from marine algae Cladosiphon okamuranus (o-fucoidan and Kjellamaniella crassifolia (t-fucoidan were used for synthesis of AuNPs. The suitable condition for the synthesis was investigated to obtain the nanometric size of AuNPs. The synthesized AuNPs were characterized for the size, morphology and Surface Plasmon Resonance (SPR. Results: The fucoidan-stabilized AuNPs containing optimum weight ratio of gold atom to fucoidan yielded the spherical sizes with an average of 8-10 nm and the absorption maxima of SPR band around 527-530 nm. The AuNPs stabilized by o-fucoidan structured as linear polymer were more monodisperse than those stabilized by t-fucoidan structured as branched polymer. Conclusion: Fucoidan can be employed solely for AuNP synthesis and the sulfate constituent in fucoidan is important for gold reduction and stabilization. The simple yet eco-friendly synthesis of AuNPs stabilized by fucoidans would be attractive for application use of metallic nanoparticles.

  19. Facile Synthesis of Curcumin-Loaded Starch-Maleate Nanoparticles

    OpenAIRE

    Suh Cem Pang; Soon Hiang Tay; Suk Fun Chin

    2014-01-01

    We have demonstrated the loading of curcumin onto starch maleate (SM) under mild conditions by mixing dissolved curcumin and SM nanoparticles separately in absolute ethanol and ethanol/aqueous (40 : 60 v/v), respectively. Curcumin-loaded starch-maleate (CurSM) nanoparticles were subsequently precipitated from a homogeneous mixture of these solutions in absolute ethanol based on the solvent exchange method. TEM analysis indicated that the diameters of CurSM nanoparticles were ranged between 30...

  20. Chitosan nanoparticles synthesis caught in action using microdroplet reactions

    Science.gov (United States)

    Kamat, Vivek; Bodas, Dhananjay; Paknikar, Kishore

    2016-02-01

    The ionic gelation process for the synthesis of chitosan nanoparticles was carried out in microdroplet reactions. The synthesis could be stopped instantaneously at different time points by fast dilution of the reaction mixture with DI water. Using this simple technique, the effect of temperature and reactant concentrations on the size and distribution of the nanoparticles formed, as a function of time, could be investigated by DLS and SEM. Results obtained indicated very early (1-5 s) nucleation of the particles followed by growth. The concentration of reactants, reaction temperature as well as time, were found to (severally and collectively) determine the size of nanoparticles and their distribution. Nanoparticles obtained at 4 °C were smaller (60-80 nm) with narrower size distribution. Simulation experiments using Comsol software showed that at 4 °C ‘droplet synthesis’ of nanoparticles gets miniaturised to ‘droplet-core synthesis’, which is being reported for the first time.

  1. One step facile synthesis of ferromagnetic magnetite nanoparticles

    Science.gov (United States)

    Suppiah, Durga Devi; Abd Hamid, Sharifah Bee

    2016-09-01

    The ferromagnetic properties of magnetite (Fe3O4) were influenced by the nanoparticle size, hence importance were given to the synthesis method. This paper clearly shows that magnetite nanoparticles were successfully synthesized by employing one step controlled precipitation method using a single salt (Iron(II) sulfate) iron precursor. The acquired titration curve from this method provides vital information on the possible reaction mechanism leading to the magnetite (Fe3O4) nanoparticles formation. Goethite (α-FeOOH) was obtained at pH 4, while the continuous addition of hydroxyl ions (OH-) forms iron hydroxides (Fe(OH)2). This subsequently reacts with the goethite, producing magnetite (Fe3O4) at pH 10. Spectroscopy studies validate the magnetite phase existence while structural and morphology analysis illustrates cubic shaped magnetite with an average size of 35 nm was obtained. The synthesized magnetite might be superparamagnetic though lower saturation magnetization (67.5 emu/g) measured at room temperature as compared to bulk magnetite. However the nanoparticles surface anisotropy leads to higher remanence (12 emu/g) and coercivity (117.7 G) making the synthesized magnetite an excellent candidate to be utilized in recording devices. The understanding of the magnetite synthesis mechanism can not only be used to achieve even smaller magnetite nanoparticles but also to prepare different types of iron oxides hydroxides using different iron precursor source.

  2. Synthesis and electrochemical characterization of stabilized nickel nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Dominguez-Crespo, M.A.; Ramirez-Meneses, E.; Torres Huerta, A.M. [Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada, CICATA-IPN Unidad Altamira, Carretera Tampico-Puerto Industrial, C.P. 89600 Altamira, Tamaulipas (Mexico); Montiel-Palma, V. [Centro de Investigaciones Quimicas, Universidad Autonoma del Estado de Morelos, Av. Universidad 1001, Colonia Chamilpa, C.P.62201 Cuernavaca, Morelos (Mexico); Dorantes Rosales, H. [Departamento de Metalurgia, Escuela Superior de Ingenieria Quimica e Industrias Extractivas - IPN, C.P. 07300, D.F. (Mexico)

    2009-02-15

    Nickel stabilized nanoparticles produced by an organometallic approach (Chaudret's method) starting from the complex Ni(1,5-COD){sub 2} were used as electrode materials for hydrogen evolution in NaOH at two temperatures (298 and 323 K). The synthesis of the nickel nanoparticles was performed in the presence of two different stabilizers, 1,3-diaminopropane (DAP) and anthranilic acid (AA), by varying the molar ratios (1:1, 1:2 and 1:5 metal:ligand) in order to evaluate their influence on the shape, dispersion, size and electrocatalytic activity of the metallic particles. The presence of an appropriate amount of stabilizer is an effective alternative to the synthesis of small monodispersed metal nanoparticles with diameters around 5 and 8 nm for DAP and AA, respectively. The results are discussed in terms of morphology and the surface state of the nanoparticles. The importance of developing a well-controlled synthetic method which results in higher performances of the resulting nanoparticles is highlighted. Herein we found that the performance with respect to the HER of the Ni electrodes dispersed on a carbon black Vulcan substrate is active and comparable to that reported in the literature for the state-of-the-art electrocatalysts. Appreciable cathodic current densities of {proportional_to}240 mA cm{sup -2} were measured with highly dispersed nickel particles (Ni-5{sub DAP}). This work demonstrates that the aforementioned method can be extended to the preparation of highly active stabilized metal particles without inhibiting the electron transfer for the HER reaction, and it could also be applied to the synthesis of bimetallic nanoparticles. (author)

  3. In situ synthesis and characterization of magnetic nanoparticles in shells of biodegradable polyelectrolyte microcapsules

    Energy Technology Data Exchange (ETDEWEB)

    Lyubutin, I.S. [Shubnikov Institute of Crystallography, Russian Academy of Sciences, Leninsky av. 59, Moscow 119333 (Russian Federation); Starchikov, S.S., E-mail: sergey.s.starchikov@gmail.com [Shubnikov Institute of Crystallography, Russian Academy of Sciences, Leninsky av. 59, Moscow 119333 (Russian Federation); Bukreeva, T.V. [Shubnikov Institute of Crystallography, Russian Academy of Sciences, Leninsky av. 59, Moscow 119333 (Russian Federation); Lysenko, I.A. [National Research Center “Kurchatov Institute”, pl. Akademika Kurchatova 1, Moscow 123182 (Russian Federation); Sulyanov, S.N.; Korotkov, N.Yu.; Rumyantseva, S.S.; Marchenko, I.V.; Funtov, K.O. [Shubnikov Institute of Crystallography, Russian Academy of Sciences, Leninsky av. 59, Moscow 119333 (Russian Federation); Vasiliev, A.L. [Shubnikov Institute of Crystallography, Russian Academy of Sciences, Leninsky av. 59, Moscow 119333 (Russian Federation); National Research Center “Kurchatov Institute”, pl. Akademika Kurchatova 1, Moscow 123182 (Russian Federation)

    2014-12-01

    Hollow microcapsules with the shell composed of biodegradable polyelectrolytes modified with the maghemite nanoparticles were fabricated by in situ synthesis. The nanoparticles were synthesized from the iron salt and the base directly on the capsule shells prepared by “layer by layer” technique. An average diameter of the capsule was about 6.7 μm while the average thickness of the capsule shell was 0.9 μm. XRD, HRTEM, Raman and Mössbauer spectroscopy data revealed that the iron oxide nanoparticles have the crystal structure of maghemite γ-Fe{sub 2}O{sub 3}. The nanoparticles were highly monodisperse with medium size of 7.5 nm. The Mössbauer spectroscopy data revealed that the nanoparticles have marked superparamagnetic behavior which was retained up to room temperature due to slow spin relaxation. Because of that, the microcapsules can be handled by an external magnetic field. Both these properties are important for target drug delivery. Based on the Mössbauer spectroscopy data, the spin blocking temperatures T{sub B} of about 90 K was found for the particles with size D ≤ 5 nm and T{sub B} ≈ 250 K for particles with D ≥ 6 nm. The anisotropy constants K were determined using the superparamagnetic approximation and in the low temperature approximation of collective magnetic excitation. - Highlights: • Hollow biodegradable microcapsules for target drug delivery • Modification of microcapsules by the maghemite nanoparticles by in situ synthesis • The nanoparticles are highly monodisperse with medium size of 7.5 nm. • Superparamagnetic properties of nanoparticles remain up to room temperature. • The spin blocking temperatures T{sub B} and the anisotropy constants K are determined.

  4. Synthesis of magnetic rhenium sulfide composite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Tang Naimei [Division of Molecular and Materials Simulation, Key Lab for Nanomaterials, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Tu Weixia [Division of Molecular and Materials Simulation, Key Lab for Nanomaterials, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China)], E-mail: tuwx@mail.buct.edu.cn

    2009-10-15

    Rhenium sulfide nanoparticles are associated with magnetic iron oxide through coprecipitation of iron salts with tetramethylammonium hydroxide. Sizes of the formed magnetic rhenium sulfide composite particles are in the range 5.5-12.5 nm. X-ray diffraction and energy-dispersive analysis of X-rays spectra demonstrate the coexistence of Fe{sub 3}O{sub 4} and ReS{sub 2} in the composite particle, which confirm the formation of the magnetic rhenium sulfide composite nanoparticles. The association of rhenium sulfide with iron oxide not only keeps electronic state and composition of the rhenium sulfide nanoparticles, but also introduces magnetism with the level of 24.1 emu g{sup -1} at 14 kOe. Surface modification with monocarboxyl-terminated poly(ethylene glycol) (MPEG-COOH) has the role of deaggregating the composite nanoparticles to be with average hydrodynamic size of 27.3 nm and improving the dispersion and the stability of the composite nanoparticles in water.

  5. Progress in electrochemical synthesis of magnetic iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ramimoghadam, Donya; Bagheri, Samira, E-mail: samira_bagheri@um.edu.my; Hamid, Sharifah Bee Abd

    2014-11-15

    Recently, magnetic iron oxide particles have been emerged as significant nanomaterials due to its extensive range of application in various fields. In this regard, synthesis of iron oxide nanoparticles with desirable properties and high potential applications are greatly demanded. Therefore, investigation on different iron oxide phases and their magnetic properties along with various commonly used synthetic techniques are remarked and thoroughly described in this review. Electrochemical synthesis as a newfound method with unique advantages is elaborated, followed by design approaches and key parameters to control the properties of the iron oxide nanoparticles. Additionally, since the dispersion of iron oxide nanoparticles is as important as its preparation, surface modification issue has been a serious challenge which is comprehensively discussed using different surfactants. Despite the advantages of the electrochemical synthesis method, this technique has been poorly studied and requires deep investigations on effectual parameters such as current density, pH, electrolyte concentration etc. - Highlights: • IONPs are applied in chemical industries, medicine, magnetic storage etc. • Electrochemical synthesis (EC) is convenient, eco-friendly, selective and low-cost. • EC key factors are current density, pH, electrolyte concentration, electrode type. • Organic, inorganic and biological materials can be used to modify IONPs’ surface. • The physicochemical properties of IONPs can be controlled by adding surfactants.

  6. Bio-mediated synthesis, characterization and cytotoxicity of gold nanoparticles.

    Science.gov (United States)

    Klekotko, Magdalena; Matczyszyn, Katarzyna; Siednienko, Jakub; Olesiak-Banska, Joanna; Pawlik, Krzysztof; Samoc, Marek

    2015-11-21

    We report here a "green" approach for the synthesis of gold nanoparticles (GNPs) in which the Mentha piperita extract was applied for the bioreduction of chloroauric acid and the stabilization of the formed nanostructures. The obtained GNPs were characterized by UV-Vis absorption spectroscopy and transmission electron microscopy (TEM). The reduction of gold ions with the plant extract leads to the production of nanoparticles with various shapes (spherical, triangular and hexagonal) and sizes (from 10 to 300 nm). The kinetics of the reaction was monitored and various conditions of the synthesis were investigated. As a result, we established protocols optimized towards the synthesis of nanospheres and nanoprisms of gold. The cytotoxic effect of the obtained gold nanoparticles was studied by performing MTT assay, which showed lower cytotoxicity of the biosynthesized GNPs compared to gold nanorods synthesized using the usual seed-mediated growth. The results suggest that the synthesis using plant extracts may be a useful method to produce gold nanostructures for various biological and medical applications. PMID:26456245

  7. Green synthesis of gold nanoparticles using Trigonella foenum-graecum and its size-dependent catalytic activity

    Science.gov (United States)

    Aswathy Aromal, S.; Philip, Daizy

    2012-11-01

    The development of new synthesis methods for monodispersed nanocrystals using cheap and nontoxic chemicals, environmentally benign solvents and renewable materials remains a challenge to the scientific community. Most of the current methods involve known protocols which may be potentially harmful to either environment or human health. Recent research has been focused on green synthesis methods to produce new nanomaterials, ecofriendly and safer with sustainable commercial viability. The present work reports the green synthesis of gold nanoparticles using the aqueous extract of fenugreek (Trigonella foenum-graecum) as reducing and protecting agent. The pathway is based on the reduction of AuCl4- by the extract of fenugreek. This method is simple, efficient, economic and nontoxic. Gold nanoparticles having different sizes in the range from 15 to 25 nm could be obtained by controlling the synthesis parameters. The nanoparticles have been characterized by UV-Visible spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD) and FTIR analysis. The high crystallinity of nanoparticles is evident from clear lattice fringes in the HRTEM images, bright circular spots in the SAED pattern and peaks in the XRD pattern. FTIR spectrum indicates the presence of different functional groups present in the biomolecule capping the nanoparticles. The synthesized gold nanoparticles show good catalytic activity for the reduction of 4-nitrophenol to 4-aminophenol by excess NaBH4. The catalytic activity is found to be size-dependent, the smaller nanoparticles showing faster activity.

  8. SYNTHESIS AND APPLICATION OF NANOPARTICLES BY A HIGH GRAVITY METHOD

    Institute of Scientific and Technical Information of China (English)

    Lei; Shao; Jianfeng; Chen

    2005-01-01

    Fast chemical reactions involved in nanomaterials synthesis, polymerization, special chemicals production, reactive absorption, etc., are often difficult to control in terms of product quality, process efficiency and production consistency.After a theoretical analysis on such processes based on chemical reaction engineering fundamentals, an idea to intensify micromixing (mixing on the molecular scale) and mass transfer and therefore to control the process ideally was proposed.By experimental investigations of mass transfer and micromixing characteristics in the Rotating Packed Bed (RPB, or "HIGEE" device), we achieved unique intense micromixing. This led us to the invention of using RPB as a reactor for the fabrication of nanoparticles (Chen et al., 2000).RPB consists mainly of a rotating packed rotator inside a stationary casing. The high gravity environment created by the RPB, which could be orders of magnitude larger than gravity, causes aqueous reactants going through the packing to spread or split into micro or nano droplets, threads or thin films, thus markedly intensifying mass transfer and micromixing to the extent of 1 to 3 orders of magnitude larger than that in a conventional packed bed.In 1994, the first RPB reactor was designed to synthesize nanoparticles of CaCO3 through multiphase reaction between Ca(OH)2 slurry and CO2 gas, and nanoparticles of 15~30nm in mean size and with very uniform particle size distribution was obtained. In 1997, a pilot-scale RPB reactor was successfully set up for operation, and in 2000, the first commercial-scale RPB reactor for synthesis of such nanoparticles came into operation in China, establishing a milestone in the use of RPB as a reactor for the fabrication of nanomaterials (Chen et al., 2002).Since then, the high gravity method has been employed for the synthesis of inorganic and organic nanoparticles via gas-liquid, liquid-liquid, and gas-liquid-solid multiphase reactions, e.g. inorganic nanoparticles like

  9. Room temperature synthesis of colloidal platinum nanoparticles

    Indian Academy of Sciences (India)

    G Sarala Devi; V J Rao

    2000-12-01

    Efficient preparation of stable dispersions of platinum nanoparticles from platinous chloride (K2PtCl4) was achieved by simultaneous addition of capping polymer material. The size of platinum nanoparticles was controlled by changing the ratio of concentration of capping polymer material to the concentration of platinum cation used. The morphology of colloidal particles were studied by means of UV-visible spectrophotometry and transmission electron microscopy (TEM). Particle size increased with low reagent concentration. The change in absorption spectra with the particle size was observed, i.e. blue shift attributed to decrease in particle size.

  10. Microbially supported synthesis of catalytically active bimetallic Pd-Au nanoparticles

    DEFF Research Database (Denmark)

    Hosseinkhani, Baharak; Søbjerg, Lina Sveidal; Rotaru, Amelia-Elena;

    2012-01-01

    Bimetallic nanoparticles are considered the next generation of nanocatalysts with increased stability and catalytic activity. Bio-supported synthesis of monometallic nanoparticles has been proposed as an environmentally friendly alternative to the conventional chemical and physical protocols. In ...

  11. Controllable synthesis of rice-shape Alq3 nanoparticles with single crystal structure

    Science.gov (United States)

    Xie, Wanfeng; Fan, Jihui; Song, Hui; Jiang, Feng; Yuan, Huimin; Wei, Zhixian; Ji, Ziwu; Pang, Zhiyong; Han, Shenghao

    2016-10-01

    We report the controllable growth of rice-shape nanoparticles of Alq3 by an extremely facile self-assembly approach. Possible mechanisms have been proposed to interpret the formation and controlled process of the single crystal nanoparticles. The field-emission performances (turn-on field 7 V μm-1, maximum current density 2.9 mA cm-2) indicate the potential application on miniaturized nano-optoelectronics devices of Alq3-based. This facile method can potentially be used for the controlled synthesis of other functional complexes and organic nanostructures.

  12. Synthesis and conjugation of ZnO nanoparticles with bovine serum albumin for biological applications

    Science.gov (United States)

    Kumar, Pawan; Kumar, Parveen; Deep, Akash; Bharadwaj, Lalit M.

    2013-04-01

    Semiconductor nanomaterials tagged with biomarkers may be used for an early fluorescence-based detection of breast cancer. ZnO nanoparticles are water-soluble, non-toxic, photo-chemically stable with highly fluorescence applicability and are regarded for their possible biocompatibility. As a long-term research planning, we are aiming to use QDs conjugated with serum-biomarker for the diagnosis of breast cancer. The present work is a part in the said direction and reports preliminary observations on the synthesis and conjugation of ZnO nanoparticles with a representative protein marker.

  13. THERMODYNAMIC AND PARTICLE-DYNAMIC STUDY FOR COMBUSTION SYNTHESIS OF TITANIA NANOPARTICLES

    Institute of Scientific and Technical Information of China (English)

    Ruoyu Hong; Zhiqiang Ren; Hongzhong Li

    2004-01-01

    Recent referential studies on combustion synthesis of titania nanoparticles were briefly reviewed. Computations based on the minimization of Gibbs free energy were conducted to find the equilibrium compositions, the optimal reaction temperature, the suitable mole ratio of oxygen to titanium tetrachloride, and the best inlet positions of titanium tetrachloride. The mean particle diameter was obtained from particle-dynamic simulation. A combustion apparatus was setup to synthesize titania nanoparticles by the oxidation and hydrolysis of titanium tetrachloride at high temperatures. Experimental investigation verified some results obtained from thermodynamic and particle-dynamic computations.

  14. Novel Cubic Magnetite Nanoparticle Synthesis Using Room Temperature Ionic Liquid

    Directory of Open Access Journals (Sweden)

    M. Sundrarajan

    2012-01-01

    Full Text Available Room Temperature Ionic liquids are relatively more useful in the synthesis of inorganic nanostructured materials because of their unique properties. To synthesize the iron oxide nanoparticle in simple precipitation method, a novel ionic liquid was used as the greener medium and stabilizing agent namely “1-n-butyl-3-methylimidazolium trifluoromethane sulfonate [BMIM][TfO]”. The crystallinity, chemical structure, morphology and magnetic properties of the synthesized magnetite nanoparticles have been characterized by using X-ray diffraction (XRD, Fourier Transform Infrared (FT-IR, Scanning electron microscopy (SEM, Atomic force microscopy(AFM, Transmission electron microscopy (TEM and Vibrating sample magnetometer (VSM studies. The XRD study is divulge that the synthesized magnetite nanoparticles have inverse spinel face centered cubic structure. The FT-IR vibration peaks show the formation of Fe3O4 nanoparticles, where the vibration peak for Fe-O is deliberately presence at 584 cm-1. The average particle size of the synthesized nanoparticles is found to be 35 nm. Homogeneously dispersed cubic shape with superstructure is found through SEM, AFM and TEM examination studies. The synthesized iron oxide nanoparticles have a high saturation magnetization value of 25 emu/g, which is very much useful for biomedical applications.

  15. Synthesis and characterization of hollow nanoparticles of crystalline Gd{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jong Hui; Jung, Yun Ku; Lee, Jin-Kyu, E-mail: jinklee@snu.ac.kr [Seoul National University, Department of Chemistry (Korea, Republic of)

    2011-06-15

    Although Gd{sub 2}O{sub 3} (gadolinia) nanoparticle is the subject of intense research interest due to its magnetic property as well as controllable emission wavelengths by doping of various lanthanide ions, it is known to be difficult to prepare monodisperse crystalline gadolinia nanoparticles because it requires high temperature thermal annealing process to enhance the crystallinity. In this article, we demonstrate the synthesis of hollow nanoparticles of crystalline Gd{sub 2}O{sub 3} by employing poly(N-vinylpyrrolidone) (PVP) to stabilize the surface of Gd(OH)CO{sub 3}{center_dot}H{sub 2}O nanoparticles and to successively form SiO{sub 2} shell as a protecting layer to prevent aggregation during calcinations processes. Silica shells could be selectively removed after calcinations by a treatment with basic solution to give hollow nanoparticles of crystalline Gd{sub 2}O{sub 3}. The formation mechanism of hollow nanoparticles could be suggested based on several characterization results of the size and shape, and crystallinity of Gd{sub 2}O{sub 3} nanoparticles by TEM, SEM, and XRD.

  16. Synthesis and characterization of hollow nanoparticles of crystalline Gd2O3

    International Nuclear Information System (INIS)

    Although Gd2O3 (gadolinia) nanoparticle is the subject of intense research interest due to its magnetic property as well as controllable emission wavelengths by doping of various lanthanide ions, it is known to be difficult to prepare monodisperse crystalline gadolinia nanoparticles because it requires high temperature thermal annealing process to enhance the crystallinity. In this article, we demonstrate the synthesis of hollow nanoparticles of crystalline Gd2O3 by employing poly(N-vinylpyrrolidone) (PVP) to stabilize the surface of Gd(OH)CO3·H2O nanoparticles and to successively form SiO2 shell as a protecting layer to prevent aggregation during calcinations processes. Silica shells could be selectively removed after calcinations by a treatment with basic solution to give hollow nanoparticles of crystalline Gd2O3. The formation mechanism of hollow nanoparticles could be suggested based on several characterization results of the size and shape, and crystallinity of Gd2O3 nanoparticles by TEM, SEM, and XRD.

  17. Recent Advances in the Synthesis and Stabilization of Nickel and Nickel Oxide Nanoparticles: A Green Adeptness

    OpenAIRE

    Imran Din, Muhammad; Rani, Aneela

    2016-01-01

    Green protocols for the synthesis of nanoparticles have been attracting a lot of attention because they are eco-friendly, rapid, and cost-effective. Nickel and nickel oxide nanoparticles have been synthesized by green routes and characterized for impact of green chemistry on the properties and biological effects of nanoparticles in the last five years. Green synthesis, properties, and applications of nickel and nickel oxide nanoparticles have been reported in the literature. This review summa...

  18. Synthesis of Functionalized Iron Oxide Nanoparticle with Amino Pyridine Moiety and Studies on Their Catalytic Behavior

    OpenAIRE

    Girija, D.; Naik, Halehatty S. Bhojya; Kumar, B. Vinay; Sudhamani, C. N.

    2011-01-01

    Aim: The main objective of this paper is to study the synthesis of functionalized iron oxide nanoparticle and its reactivity towards chromene synthesis Study design: Functionalized iron oxide nanoparticle study. Place and duration of study: Department of Studies and Research in Industrial Chemistry, School of Chemical Sciences, Kuvempu University, Shankaraghatta, between December 2009 and July 2010. Methodology: This paper describes synthesis of stable functionalized iron oxide nanoparticles ...

  19. Prodigious Effects of Concentration Intensification on Nanoparticle Synthesis: A High-Quality, Scalable Approach.

    Science.gov (United States)

    Williamson, Curtis B; Nevers, Douglas R; Hanrath, Tobias; Robinson, Richard D

    2015-12-23

    Realizing the promise of nanoparticle-based technologies demands more efficient, robust synthesis methods (i.e., process intensification) that consistently produce large quantities of high-quality nanoparticles (NPs). We explored NP synthesis via the heat-up method in a regime of previously unexplored high concentrations near the solubility limit of the precursors. We discovered that in this highly concentrated and viscous regime the NP synthesis parameters are less sensitive to experimental variability and thereby provide a robust, scalable, and size-focusing NP synthesis. Specifically, we synthesize high-quality metal sulfide NPs (200 g) relative to the current field of large-scale (0.1-5 g yields) and laboratory-scale (<0.1 g) efforts. Compared to conventional synthesis methods (hot injection with dilute precursor concentration) characterized by rapid growth and low yield, our highly concentrated NP system supplies remarkably controlled growth rates and a 10-fold increase in NP volumetric production capacity (86 g/L). The controlled growth, high yield, and robust nature of highly concentrated solutions can facilitate large-scale nanomanufacturing of NPs by relaxing the synthesis requirements to achieve monodisperse products. Mechanistically, our investigation of the thermal and rheological properties and growth rates reveals that this high concentration regime has reduced mass diffusion (a 5-fold increase in solution viscosity), is stable to thermal perturbations (∼64% increase in heat capacity), and is resistant to Ostwald ripening.

  20. Dye-doped silica-based nanoparticles for bioapplications

    International Nuclear Information System (INIS)

    This paper presents our recent research results on synthesis and bioapplications of dye-doped silica-based nanoparticles. The dye-doped water soluble organically modified silicate (ORMOSIL) nanoparticles (NPs) with the size of 15–100 nm were synthesized by modified Stöber method from methyltriethoxysilane CH3Si(OCH3)3 precursor (MTEOS). Because thousands of fluorescent dye molecules are encapsulated in the silica-based matrix, the dye-doped nanoparticles are extremely bright and photostable. Their surfaces were modified with bovine serum albumin (BSA) and biocompatible chemical reagents. The highly intensive luminescent nanoparticles were combined with specific bacterial and breast cancer antigen antibodies. The antibody-conjugated nanoparticles can identify a variety of bacterium, such as Escherichia coli O157:H7, through antibody–antigen interaction and recognition. A highly sensitive breast cancer cell detection has been achieved with the anti-HER2 monoclonal antibody–nanoparticles complex. These results demonstrate the potential to apply these fluorescent nanoparticles in various biodetection systems. (reviews)

  1. Rapid Nanoparticle Synthesis by Magnetic and Microwave Heating

    OpenAIRE

    Viktor Chikan; McLaurin, Emily J.

    2016-01-01

    Traditional hot-injection (HI) syntheses of colloidal nanoparticles (NPs) allows good separation of the nucleation and growth stages of the reaction, a key limitation in obtaining monodisperse NPs, but with limited scalability. Here, two methods are presented for obtaining NPs via rapid heating: magnetic and microwave-assisted. Both of these techniques provide improved engineering control over the separation of nucleation and growth stages of nanomaterial synthesis when the reaction is initia...

  2. Synthesis of silver nanoparticle using Portulaca oleracea L. extracts

    Directory of Open Access Journals (Sweden)

    Shahbazi Nafeseh

    2013-09-01

    Full Text Available   Objective(s: To evaluate the influences of aqueous extracts of plant parts (stem, leaves, and root of Portulaca oleracea L. on bioformation of silver nanoparticles (AgNPs.   Materials and Methods: Synthesis of silver nanoparticles by different plant part extracts of Portulaca oleracea L. was carried out and formation of nanoparticles were confirmed and evaluated using UV-Visible spectroscopy and AFM. Results: The plant extracts exposed with silver nitrate showed gradual change in color of the extract from yellow to dark brown. Different silver nanoperticles were formed using extracts of different plant parts. Conclusion: It seems that the plant parts differ in their ability to act as a reducing and capping agent.

  3. Synthesis of new dental nanocomposite with glass nanoparticles

    Directory of Open Access Journals (Sweden)

    Marzieh Monfared

    2013-09-01

    Full Text Available Objective(s: The aim of this study was to synthesis new dental nanocomposites reinforced with fabricated glass nanoparticles and compare two methods for fabrication and investigate the effect of this filler on mechanical properties. Materials and Methods : The glass nanoparticles were produced by wet milling process. The particle size and shape was achieved using PSA and SEM. Glass nanoparticles surface was modified with MPTMS silane. The composite was prepared by mixing these silane-treated nanoparticles with monomers. The resin composition was UDMA /TEGDMA (70/30 weight ratio. Three composites were developed with 5, 7.5 and 10 wt% glass fillers in each group. Two preparation methods were used, in dispersion in solvent method (group D glass nanoparticles were sonically dispersed in acetone and the solution was added to resin, then acetone was evaporated. In non-dispersion in solvent method (group N the glass nanoparticles were directly added to resin. Mechanical properties were investigated included flexural strength, flexural modulus and Vickers hardness. Results: Higher volume of glass nanoparticles improves mechanical properties of composite. Group D has batter mechanical properties than group N. Flexural strength of composite with 10%w filler of group D was 75Mpa against 59 Mpa of the composite with the same filler content of group N. The flexural modulus and hardness of group D is more than group N. Conclusion: It can be concluded that dispersion in solvent method is the best way to fabricate nanocomposites and glass nanoparticles is a significant filler to improve mechanical properties of dental nanocomposite.

  4. Liposomal nanoreactors for the synthesis of monodisperse palladium nanoparticles using glycerol.

    Science.gov (United States)

    Clergeaud, Gael; Genç, Rükan; Ortiz, Mayreli; O'Sullivan, Ciara K

    2013-12-10

    The synthesis of highly stable ultrasmall monodisperse populations of palladium nanoparticles in the range of 1-3 nm in size was achieved via polyol reduction within 1,2-dioleoyl-sn-glycero-3-phosphor-rac-(1-glycerol) liposomal nanoreactors exploiting glycerol as both reducing and stabilizing agent. The liposome-based green method was compared with synthesis in solution, and the reducing agent concentration and the lipidic composition of the liposomal nanoreactors were demonstrated to have a strong effect on the final size and homogeneity of the palladium nanoparticles. Glycerol molecules acting as capping agent demonstrated the ability to stabilize the palladium nanoparticles over a long period of time, maintaining their homogeneity in size and shape. The obtained palladium nanoparticles were characterized using transmission electron microscopy, selected area electron diffraction, Fourier transform infrared and Raman spectroscopies, X-ray diffraction, and dynamic light scattering to determine their morphology, size, charge, surface chemistry, and crystal structure. The catalytic activity of the palladium nanoparticles was also tested for a reduction reaction. PMID:24246054

  5. Sol - Gel synthesis and characterization of magnesium peroxide nanoparticles

    Science.gov (United States)

    Jaison, J.; Ashok raja, C.; Balakumar, S.; Chan, Y. S.

    2015-04-01

    Magnesium peroxide is an excellent source of oxygen in agriculture applications, for instance it is used in waste management as a material for soil bioremediation to remove contaminants from polluted underground water, biological wastes treatment to break down hydrocarbon, etc. In the present study, sol-gel synthesis of magnesium peroxide (MgO2) nanoparticles is reported. Magnesium peroxide is odourless; fine peroxide which releases oxygen when reacts with water. During the sol-gel synthesis, the magnesium malonate intermediate is formed which was then calcinated to obtain MgO2 nanoparticles. The synthesized nanoparticles were characterized using Thermo gravimetric -Differential Thermal Analysis (TG- DTA), X-Ray Diffraction studies (XRD) and High Resolution Transmission Electron Microscope (HRTEM). Our study provides a clear insight that the formation of magnesium malonate during the synthesis was due to the reaction between magnesium acetate, oxalic acid and ethanol. In our study, we can conclude that the calcination temperature has a strong influence on particle size, morphology, monodispersity and the chemistry of the particles.

  6. Synthesis and applications of novel silver nanoparticle structures

    Science.gov (United States)

    Dukes, Kyle

    template base self assembly. A 1.5 micron silica sphere is bound to poly(4-vinylpyridine) coated glass and used as a template. a mask of silica monoxide is vacuum deposited atop the spheres/glass leaving a ring just below the sphere untouched and able to bind silver nanoparticles. Optical microscopy reveal interesting results under depolarized light conditions, but ultimate structural analysis has proven elusive. Semiconducting p-type cuprous oxide was electrochemically deposited on both silver and indium tin oxide electrodes. Silver nanoparticles were incorporated into the architecture either atop the cuprous oxide or sandwiched between cuprous oxide and n-type material. Increases in photocurrent were observed in both cases and further work must be conducted to optimize a solid state device for photovoltaic applications.

  7. Synthesis of Nano-Particles in Flames

    DEFF Research Database (Denmark)

    Johannessen, Tue

    The scope of this work is to investigate the synthesis of aluminum oxide particles in flames from the combustion of an aluminum alkoxide precursor.A general introduction to particles formation in the gas phase is presented with emphasis on the mechanisms that control the particle morphology after...... energy expression.Furthermore, the model is validated by comparison with experimental data of the flame synthesis of titania by combustion of TiCl4 previously presented by Pratsinis et al. (1996).The combination of particle dynamics and CFD simulations has proved to be an efficient method...

  8. Synthesis and Characterization of Chromium Oxide Nanoparticles

    OpenAIRE

    Vivek Sheel Jaswal; Avnish Kumar Arora; Joginder Singh; Mayank Kinger; Vishnu Dev Gupta

    2014-01-01

    Chromium oxide nanoparticles (NPs)have been rapidly synthesized by precipitation method using ammomia as precipitating agent and are characterized by using X-ray Diffraction (XRD), Thermo Gravimetric Analysis (TGA), UV-Visible absorption (UV), Infrared Spectoscopy (IR), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). XRD studies show that chromium oxide NP is formed as Cr2O3 and it has hexagonal structure. The shape and particle size of the synthesized Cr2O3 NP...

  9. Synthesis and antimicrobial effects of silver nanoparticles

    Directory of Open Access Journals (Sweden)

    S kheybari

    2010-09-01

    Full Text Available "n  "n "nBackground and the purpose of the study:The most prominent nanoparticles for medical uses are nanosilver particles which are famous for their high anti-microbial activity. Silver ion has been known as a metal ion that exhibit anti-mold, anti-microbial and anti-algal properties for a long time. In particular, it is widely used as silver nitrate aqueous solution which has disinfecting and sterilizing actions. The purpose of this study was to evaluate the antimicrobial activity as well as physical properties of the silver nanoparticles prepared by chemical reduction method. "nMethods:Silver nanoparticles (NPs were prepared by reduction of silver nitrate in the presence of a reducing agent and also poly [N-vinylpyrolidone] (PVP as a stabilizer. Two kinds of NPs were synthesized by ethylene glycol (EG and glucose as reducing agent. The nanostructure and particle size of silver NPs were confirmed by scanning electron microscopy (SEM and laser particle analyzer (LPA. The formations of the silver NPs were monitored using ultraviolet-visible spectroscopy. The anti-bacterial activity of silver NPs were assessed by determination of their minimum inhibitory concentrations (MIC against the Gram positive (Staphylococcus aureus and Staphylococcus epidermidis as well as Gram-negative (Escherichia coli and Pseudomonas aeruginosa bacteria. "nResults and Conclusion:The silver nanoparticles were spherical with particle size between 10 to 250 nm. Analysis of the theoretical (Mie light scattering theory and experimental results showed that the silver NPs in colloidal solution had a diameter of approximately 50 nm. "nBoth colloidal silver NPs showed high anti-bacterial activity against Gram positive and Gram negative bacteria. Glucose nanosilver colloids showed a shorter killing time against most of the tested bacteria which could be due to their nanostructures and uniform size distribution patterns.

  10. Synthesis of photoluminescent carbon nanoparticles from graphite

    Energy Technology Data Exchange (ETDEWEB)

    Fu Xiaobo; Li Dianhong; Zhang Yuanming, E-mail: tzhangymjnu@163.com [School of Life Science and Technology, Jinan University, Department of Chemistry (China)

    2013-04-15

    Photoluminescent carbon nanoparticles (CNPs) with diameters ranging from 1.5 to 6.5 nm were synthesized from raw graphite without surface passivation. The photoluminescent (PL) emission spectra illustrate that both excitation wavelength and solution pH can significantly influence the maximum emission wavelength and PL intensity of the CNP solution. As the excitation wavelength decreases and solution pH increases, a blue shift in the maximum PL emission wavelength occurs.

  11. Synthesis of photoluminescent carbon nanoparticles from graphite

    International Nuclear Information System (INIS)

    Photoluminescent carbon nanoparticles (CNPs) with diameters ranging from 1.5 to 6.5 nm were synthesized from raw graphite without surface passivation. The photoluminescent (PL) emission spectra illustrate that both excitation wavelength and solution pH can significantly influence the maximum emission wavelength and PL intensity of the CNP solution. As the excitation wavelength decreases and solution pH increases, a blue shift in the maximum PL emission wavelength occurs.

  12. Synthesis and characterization of magnetic nanoparticles

    Institute of Scientific and Technical Information of China (English)

    邱星屏

    2000-01-01

    Magnetic nanoparticles with average diameter in the range of 6.4-8.3 nm have been synthesized by a chemical co-precipi-tation of Fe(Ⅱ) and Fe(Ⅲ) salts in 1.5 M NH4OH solution.The size of the magenetic particles is dependent on both temperature and the ionic strength of the iron ion solutions. The magnetic particles formed at higher temperature or lower ionic strength were slightly larger than those formed at lower temperature or higher ionic strength respectively. In spite of the different reaction co nditions, all the resultant nanopar ticles are nearly spherical and have a similar crystalline structure. At300 K, such prepared nanoparticles are superparamagnetic. The saturation magnetizations for 7.8 and 6.4 nm particles are 71 and 63 emu/g respectively, which are only -20-30% less than the saturation magnetization (90 emu/g) of bulk Fe3O4. Our results indicated that a control of the reaction conditions could be used to tailor the size of magnetic nanoparticles in free precipita tion.

  13. Streptomyces somaliensis mediated green synthesis of silver nanoparticles

    Directory of Open Access Journals (Sweden)

    Meysam Soltani Nejad

    2015-07-01

    Full Text Available Objective(s: The development of reliable and ecofriendly process for the synthesis of nano-metals is an important aspect in the field of nanotechnology. Nano-metals are a special group of materials with broad area of applications. Materials and Methods: In this study, extracellular synthesis of silver nanoparticles (SNPs performed by use of the gram positive soil Streptomycetes. Streptomycetes isolated from rice fields of Guilan Province, Iran (5 isolates. Initial characterization of SNPs was performed by visual change color. To determine the bacterium taxonomical identity, its colonies characterized morphologically by use of scanning electron microscope. The PCR molecular analysis of active isolate represented its identity partially. In this regard, 16S rDNA of isolate G was amplified using universal bacterial primers FD1 and RP2. The PCR products were purified and sequenced. Sequence analysis of 16S rDNA was then conducted using NCBI GenBank database using BLAST. Also SNPs were characterized by, transmission electron microscopy (TEM and X-ray diffraction spectroscopy (XRD. Results: From all 5 collected Streptomyces somaliensis isolates, isolate G showed highest extracellular synthesis of SNPs via in vitro. SNPs were formed immediately by the addition of (AgNO3 solution (1 mM. UV-visible spectrophotometry for measuring surface plasmon resonance showed a single absorption peak at 450 nm, which confirmed the presence of SNPs. TEM revealed the extracellular formation of spherical silver nanoparticles in the size range of 5-35 nm. Conclusions: The biological approach for the synthesis of metal nanoparticles offers an environmentally benign alternative to the traditional chemical and physical synthesis methods. So, a simple, environmentally friendly and cost-effective method has been developed to synthesize AgNPs using Streptomycetes.

  14. Applications of plant terpenoids in the synthesis of colloidal silver nanoparticles.

    Science.gov (United States)

    Mashwani, Zia-Ur-Rehman; Khan, Mubarak Ali; Khan, Tariq; Nadhman, Akhtar

    2016-08-01

    Green chemistry is the design of chemical products and processes that reduce or eliminate the generation of hazardous substances. Since the last few years, natural products especially plant secondary metabolites have been extensively explored for their potency to synthesize silver nanoparticles (AgNPs). The plant-based AgNPs are safer, energy efficient, eco-friendly, and less toxic than chemically synthesized counterparts. The secondary metabolites, ubiquitously found in plants especially the terpenoid-rich essential oils, have a significant role in AgNPs synthesis. Terpenoids belong to the largest family of natural products and are found in all kinds of organisms. Their involvement in the synthesis of plant-based AgNPs has got much attention in the recent years. The current article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present the pertinent role of plant terpenoids in the biosynthesis of AgNPs, as capping and reducing agents for development of uniform size and shape AgNPs. An emphasis on the important role of FTIR in the identification and elucidation of major functional groups in terpenoids for AgNPs synthesis has also been reviewed in this manuscript. It was found that no such article is available that has discussed the role of plant terpenoids in the green synthesis of AgNPs. PMID:27181393

  15. Silver nanoparticles: synthesis, properties, toxicology, applications and perspectives

    International Nuclear Information System (INIS)

    In recent years the outbreak of re-emerging and emerging infectious diseases has been a significant burden on global economies and public health. The growth of population and urbanization along with poor water supply and environmental hygiene are the main reasons for the increase in outbreak of infectious pathogens. Transmission of infectious pathogens to the community has caused outbreaks of diseases such as influenza (A/H5N1), diarrhea (Escherichia coli), cholera (Vibrio cholera), etc throughout the world. The comprehensive treatments of environments containing infectious pathogens using advanced disinfectant nanomaterials have been proposed for prevention of the outbreaks. Among these nanomaterials, silver nanoparticles (Ag-NPs) with unique properties of high antimicrobial activity have attracted much interest from scientists and technologists to develop nanosilver-based disinfectant products. This article aims to review the synthesis routes and antimicrobial effects of Ag-NPs against various pathogens including bacteria, fungi and virus. Toxicology considerations of Ag-NPs to humans and ecology are discussed in detail. Some current applications of Ag-NPs in water-, air- and surface- disinfection are described. Finally, future prospects of Ag-NPs for treatment and prevention of currently emerging infections are discussed. (review)

  16. Silver nanoparticles: synthesis, properties, toxicology, applications and perspectives

    Science.gov (United States)

    Tran, Quang Huy; Quy Nguyen, Van; Le, Anh-Tuan

    2013-09-01

    In recent years the outbreak of re-emerging and emerging infectious diseases has been a significant burden on global economies and public health. The growth of population and urbanization along with poor water supply and environmental hygiene are the main reasons for the increase in outbreak of infectious pathogens. Transmission of infectious pathogens to the community has caused outbreaks of diseases such as influenza (A/H5N1), diarrhea (Escherichia coli), cholera (Vibrio cholera), etc throughout the world. The comprehensive treatments of environments containing infectious pathogens using advanced disinfectant nanomaterials have been proposed for prevention of the outbreaks. Among these nanomaterials, silver nanoparticles (Ag-NPs) with unique properties of high antimicrobial activity have attracted much interest from scientists and technologists to develop nanosilver-based disinfectant products. This article aims to review the synthesis routes and antimicrobial effects of Ag-NPs against various pathogens including bacteria, fungi and virus. Toxicology considerations of Ag-NPs to humans and ecology are discussed in detail. Some current applications of Ag-NPs in water-, air- and surface- disinfection are described. Finally, future prospects of Ag-NPs for treatment and prevention of currently emerging infections are discussed.

  17. Mg(OH){sub 2} nanoparticles produced at room temperature by an innovative, facile, and scalable synthesis route

    Energy Technology Data Exchange (ETDEWEB)

    Taglieri, Giuliana, E-mail: giuliana.taglieri@univaq.it; Felice, Benito; Daniele, Valeria; Ferrante, Fabiola [University of L’Aquila, Department of Industrial and Information Engineering and Economics (Italy)

    2015-10-15

    Nanoparticles form the fundamental building blocks for many exciting applications in various scientific disciplines. However, the problem of the large-scale synthesis of nanoparticles remains challenging. An original, eco-friendly, single step, and scalable method to produce magnesium hydroxide nanoparticles in aqueous suspensions is here presented. The method, based on an exchange ion process, is extremely simple and rapid (few minutes). It employs cheap or renewable reactants, operates at room temperature and does not require intermediate steps (washings/purifications) to eliminate undesired compounds. Moreover, it is possible to regenerate the exchange material and to reuse it for new operation of synthesis, according to a cyclic procedure, providing potential aptitudes of scalability of nanoparticles production. Some of the synthesis parameters are varied, and structural and morphological features of the produced nanoparticles, after few seconds from the beginning of the synthesis up to the ending time, are investigated by means of several techniques, such as X-ray diffraction (profile fitting and Rietveld refinement), transmission electron microscopy, infrared spectroscopy, thermal analyses, and surface area measurements. In any case, pure and stable suspensions are produced, characterized by crystalline and mesoporous Mg(OH){sub 2} nanoparticles, with lamellar morphology. In particular, the nanolamellas appeared constituted by a superimposition of hexagonally plated and crystalline nanosized precursors (2–3 nm in dimensions), crystallographically oriented.

  18. High Surface Area Ceria Nanoparticles via Hydrothermal Synthesis Experiment Design

    Directory of Open Access Journals (Sweden)

    Stanislav Kurajica

    2016-01-01

    Full Text Available Hydrothermal synthesis of CeO2 was optimized on two reactant concentrations and synthesis temperature and duration, in order to achieve material having the greatest specific surface area (SSA. Taguchi method of experimental design was employed in evaluation of the relative importance of synthesis parameters. CeO2 nanoparticles were characterized using X-ray diffraction, nitrogen adsorption-desorption isotherms, and scanning electron microscopy. Optimum conditions for obtaining particles with greater SSA were calculated according to Taguchi’s model “the-higher-the-better.” Synthesis temperature was found to be the only parameter significant for enabling nanoparticles with greater SSA. Mesoporous nanocrystalline ceria with SSA as great as 226 m2 g−1 was achieved, which is unprecedented for the hydrothermally synthesized ceria. The reason for this achievement was found in temperature dependence of the diffusion coefficient which, when low, favors nucleation yielding with fine particles, while when high it favors crystal growth and formation of one-dimensional structures. The occurrence of 1D-structure in sample exhibiting the smallest SSA was confirmed. Very fine crystallites with crystallite size as low as 5.9 nm have been obtained being roughly inverse proportional to SSA. Selected samples were tested as catalyst for soot oxidation. Catalyst morphology turned out to be decisive factor for catalytic activity.

  19. Synthesis of Green Metallic Nanoparticles (NPs and Applications

    Directory of Open Access Journals (Sweden)

    Varahalarao Vadlapudi

    2014-01-01

    Full Text Available Nanotechnology (NT is a field that is mushrooming, making an impact in all spheres of human life. Presently available literature revealed that the NP synthesis using medicinal plants, microorganisms and algae and others as source has been unexplored and underexploited. NT is very important in developing sustainable technologies for the future, for humanity and the environment. The development of green processes for the synthesis of NP is evolving into an important branch of nanotechnology. Natural sources of nanoparticles include fires and volcanic eruptions. The nanotechnology have short to long term uses like environmental pollution cleanup, efficient and safe drug delivery mechanisms with less side effects, developments in information technology, self-cleaning window glass , ‘smart’ fabrics which adjust to suit the temperature. Plant mediated synthesis of metal nanoparticles is gaining more importance owing to its simplicity, rapid rate of synthesis of NP of attractive and diverse morphologies and elimination of elaborate maintenance of cell cultures and ecofriendliness. It has many advantages such as, ease with which the process can be measured up, economic viability and etc. Presently, the researchers are looking into the development of cost-effective procedures for producing reproducible, stable and biocompatible metal NPs.

  20. Flame spray synthesis under a non-oxidizing atmosphere: Preparation of metallic bismuth nanoparticles and nanocrystalline bulk bismuth metal

    Energy Technology Data Exchange (ETDEWEB)

    Grass, Robert N.; Stark, Wendelin J. [Institute for Chemical and Bioengineering, ETH Zuerich (Switzerland)], E-mail: wendelin.stark@chem.ethz.ch

    2006-10-15

    Metallic bismuth nanoparticles of over 98% purity were prepared by a modified flame spray synthesis method in an inert atmosphere by oxygen-deficient combustion of a bismuth-carboxylate based precursor. The samples were characterized by X-ray diffraction, thermal analysis and scanning electron microscopy confirming the formation of pure, crystalline metallic bismuth nanoparticles. Compression of the as-prepared powder resulted in highly dense, nanocrystalline pills with strong electrical conductivity and bright metallic gloss.

  1. Encapsulated Nanoparticle Synthesis and Characterization for Improved Storage Fluids: Preprint

    Energy Technology Data Exchange (ETDEWEB)

    Glatzmaier, G. C.; Pradhan, S.; Kang, J.; Curtis, C.; Blake, D.

    2010-10-01

    Nanoparticles are typically composed of 50--500 atoms and exhibit properties that are significantly different from the properties of larger, macroscale particles that have the same composition. The addition of these particles to traditional fluids may improve the fluids' thermophysical properties. As an example, the addition of a nanoparticle or set of nanoparticles to a storage fluid may double its heat capacity. This increase in heat capacity would allow a sensible thermal energy storage system to store the same amount of thermal energy in half the amount of storage fluid. The benefit is lower costs for the storage fluid and the storage tanks, resulting in lower-cost electricity. The goal of this long-term research is to create a new class of fluids that enable concentrating solar power plants to operate with greater efficiency and lower electricity costs. Initial research on this topic developed molecular dynamic models that predicted the energy states and transition temperatures for these particles. Recent research has extended the modeling work, along with initiating the synthesis and characterization of bare metal nanoparticles and metal nanoparticles that are encapsulated with inert silica coatings. These particles possess properties that make them excellent candidates for enhancing the heat capacity of storage fluids.

  2. Reviewing the Tannic Acid Mediated Synthesis of Metal Nanoparticles

    Directory of Open Access Journals (Sweden)

    Tufail Ahmad

    2014-01-01

    Full Text Available Metal nanoparticles harbour numerous exceptional physiochemical properties absolutely different from those of bulk metal as a function of their extremely small size and large superficial area to volume. Naked metal nanoparticles are synthesized by various physical and chemical methods. Chemical methods involving metal salt reduction in solution enjoy an extra edge over other protocols owing to their relative facileness and capability of controlling particle size along with the attribute of surface tailoring. Although chemical methods are the easiest, they are marred by the use of hazardous chemicals such as borohydrides. This has led to inclination of scientific community towards eco-friendly agents for the reduction of metal salts to form nanoparticles. Tannic acid, a plant derived polyphenolic compound, is one such agent which embodies characteristics of being harmless and environmentally friendly combined with being a good reducing and stabilizing agent. In this review, first various methods used to prepare metal nanoparticles are highlighted and further tannic acid mediated synthesis of metal nanoparticles is emphasized. This review brings forth the most recent findings on this issue.

  3. Highly bacterial resistant silver nanoparticles: synthesis and antibacterial activities

    Energy Technology Data Exchange (ETDEWEB)

    Chudasama, Bhupendra, E-mail: bnchudasama@gmail.co [Thapar University, School of Physics and Materials Science (India); Vala, Anjana K.; Andhariya, Nidhi; Mehta, R. V. [Bhavnagar University, Department of Physics (India); Upadhyay, R. V. [Charotar University of Science and Technology, P.D. Patel Institute of Applied Sciences (India)

    2010-06-15

    In this article, we describe a simple one-pot rapid synthesis route to produce uniform silver nanoparticles by thermal reduction of AgNO{sub 3} using oleylamine as reducing and capping agent. To enhance the dispersal ability of as-synthesized hydrophobic silver nanoparticles in water, while maintaining their unique properties, a facile phase transfer mechanism has been developed using biocompatible block co-polymer pluronic F-127. Formation of silver nanoparticles is confirmed by X-ray diffraction (XRD), transmission electron microscopy (TEM) and UV-vis spectroscopy. Hydrodynamic size and its distribution are obtained from dynamic light scattering (DLS). Hydrodynamic size and size distribution of as-synthesized and phase transferred silver nanoparticles are 8.2 {+-} 1.5 nm ({sigma} = 18.3%) and 31.1 {+-} 4.5 nm ({sigma} = 14.5%), respectively. Antimicrobial activities of hydrophilic silver nanoparticles is tested against two Gram positive (Bacillus megaterium and Staphylococcus aureus), and three Gram negative (Escherichiacoli, Proteusvulgaris and Shigellasonnei) bacteria. Minimum inhibitory concentration (MIC) values obtained in the present study for the tested microorganisms are found much better than those reported for commercially available antibacterial agents.

  4. Synthesis of manganese spinel nanoparticles at room temperature by coprecipitation

    Energy Technology Data Exchange (ETDEWEB)

    Giovannelli, F., E-mail: fabien.giovannelli@univ-tours.fr [GREMAN, UMR 7347 CNRS-CEA, Universite Francois Rabelais, 15 rue de la chocolaterie, 41000 BLOIS (France); Autret-Lambert, C.; Mathieu, C.; Chartier, T.; Delorme, F. [GREMAN, UMR 7347 CNRS-CEA, Universite Francois Rabelais, 15 rue de la chocolaterie, 41000 BLOIS (France); Seron, A [BRGM, 3 Avenue Claude Guillemin, BP 36009, 45060 ORLEANS Cedex 2 (France)

    2012-08-15

    This paper is focused on a new route to synthesize Mn{sub 3}O{sub 4} nanoparticles by alkalisation by sodium hydroxide on a manganeous solution at room temperature. The precipitates obtained at different pH values have been characterized by XRD and TEM. Since the first addition of sodium hydroxide, a white Mn(OH){sub 2} precipitate appears. At pH=7, {gamma}-MnOOH phase is predominant with needle like shaped particles. At pH=10, hausmanite nanoparticles, which exhibits well defined cubic shape in the range 50-120 nm are obtained. This new precipitation route is a fast and easy environmentally friendly process to obtain well crystallized hausmanite nanoparticles. - Graphical abstract: TEM image showing Mn{sub 3}O{sub 4} particles after a precipitation at pH=10. Highlights: Black-Right-Pointing-Pointer A new route to synthesize Mn{sub 3}O{sub 4} nanoparticles has been demonstrated. Black-Right-Pointing-Pointer Synthesis has been performed by precipitation at room temperature. Black-Right-Pointing-Pointer The size of the Mn{sub 3}O{sub 4} nanoparticles is between 50 and 120 nm.

  5. Ionic magnetic fluid based on cobalt ferrite nanoparticles: Influence of hydrothermal treatment on the nanoparticle size

    Energy Technology Data Exchange (ETDEWEB)

    Cabuil, Valerie; Dupuis, Vincent; Talbot, Delphine [UPMC Univ Paris 06, UMR 7195, PECSA, F-75005, Paris (France); CNRS, UMR 7195, PECSA, F-75005, Paris (France); Neveu, Sophie, E-mail: sophie.neveu@upmc.f [UPMC Univ Paris 06, UMR 7195, PECSA, F-75005, Paris (France); CNRS, UMR 7195, PECSA, F-75005, Paris (France)

    2011-05-15

    Magnetic fluid based on cobalt ferrite nanoparticles was obtained using a hydrothermal treatment added to the Massart procedure. This treatment increases the average size of the nanoparticles from 11.9 to 18.7 nm and also improves the dispersity and crystallinity of the cobalt ferrite particles. The nanoparticles obtained after the hydrothermal treatment were dispersed in aqueous solvent by the classical procedure for ionic magnetic fluids. The ferrofluid thus obtained is stable at pH 7 and may be useful for hyperthermia applications. - Research Highlights: Hydrothermal synthesis of cobalt ferrite ferrofluid (mean particle size of 12-19 nm). Good control of size, dispersity and crystallinity of the cobalt ferrite particles. Ferrofluid stable at pH 7 and useful for hyperthermia applications.

  6. Radiation synthesized protein-based nanoparticles: A technique overview

    International Nuclear Information System (INIS)

    Seeking for alternative routes for protein engineering a novel technique – radiation induced synthesis of protein nanoparticles – to achieve size controlled particles with preserved bioactivity has been recently reported. This work aimed to evaluate different process conditions to optimize and provide an overview of the technique using γ-irradiation. Papain was used as model protease and the samples were irradiated in a gamma cell irradiator in phosphate buffer (pH=7.0) containing ethanol (0–35%). The dose effect was evaluated by exposure to distinct γ-irradiation doses (2.5, 5, 7.5 and 10 kGy) and scale up experiments involving distinct protein concentrations (12.5–50 mg mL−1) were also performed. Characterization involved size monitoring using dynamic light scattering. Bityrosine detection was performed using fluorescence measurements in order to provide experimental evidence of the mechanism involved. Best dose effects were achieved at 10 kGy with regard to size and no relevant changes were observed as a function of papain concentration, highlighting very broad operational concentration range. Bityrosine changes were identified for the samples as a function of the process confirming that such linkages play an important role in the nanoparticle formation. - Highlights: • Synthesis of protein-based nanoparticles by γ-irradiation. • Optimization of the technique. • Overview of mechanism involved in the nanoparticle formation. • Engineered papain nanoparticles for biomedical applications

  7. ns or fs pulsed laser ablation of a bulk InSb target in liquids for nanoparticles synthesis.

    Science.gov (United States)

    Semaltianos, N G; Hendry, E; Chang, H; Wears, M L; Monteil, G; Assoul, M; Malkhasyan, V; Blondeau-Patissier, V; Gauthier-Manuel, B; Moutarlier, V

    2016-05-01

    Laser ablation of bulk target materials in liquids has been established as an alternative method for the synthesis of nanoparticles colloidal solutions mainly due to the fact that the synthesized nanoparticles have bare, ligand-free surfaces since no chemical precursors are used for their synthesis. InSb is a narrow band gap semiconductor which has the highest carrier mobility of any known semiconductor and nanoparticles of this material are useful in optoelectronic device fabrication. In this paper a bulk InSb target was ablated in deionized (DI) water or ethanol using a nanosecond (20 ns) or a femtosecond (90 fs) pulsed laser source, for nanoparticles synthesis. In all four cases the largest percentage of the nanoparticles are of InSb in the zincblende crystal structure with fcc lattice. Oxides of either In or Sb are also formed in the nanoparticles ensembles in the case of ns or fs ablation, respectively. Formation of an oxide of either element from the two elements of the binary bulk alloy is explained based on the difference in the ablation mechanism of the material in the case of ns or fs pulsed laser irradiation in which the slow or fast deposition of energy into the material results to mainly melting or vaporization, respectively under the present conditions of ablation, in combination with the lower melting point but higher vaporization enthalpy of In as compared to Sb. InSb in the metastable phase with orthorhombic lattice is also formed in the nanoparticles ensembles in the case of fs ablation in DI water (as well as oxide of InSb) which indicates that the synthesized nanoparticles exhibit polymorphism controlled by the type of the laser source used for their synthesis. The nanoparticles exhibit absorption which is observed to be extended in the infrared region of the spectrum.

  8. Bulk Synthesis and Characterization of Ti3Al Nanoparticles by Flow-Levitation Method

    Directory of Open Access Journals (Sweden)

    Shanjun Chen

    2013-01-01

    Full Text Available A novel bulk synthesis method for preparing high pure Ti3Al nanoparticles was developed by flow-levitation method (FL. The Ti and Al vapours ascending from the high temperature levitated droplet were condensed by cryogenic Ar gas under atmospheric pressure. The morphology, crystalline structure, and chemical composition of Ti3Al nanoparticles were, respectively, investigated by transmission electron microscopy, X-ray diffraction, and inductively coupled plasma atomic emission spectrometry. The results indicated that the Ti3Al powders are nearly spherical-shaped, and the particle size ranges from several nanometers to 100 nm in diameter. Measurements of the d-spacing from X-ray (XRD and electron diffraction studies confirmed that the Ti3Al nanoparticles have a hexagonal structure. A thin oxidation coating of 2-3 nm in thickness was formed around the particles after exposure to air. Based on the XPS measurements, the surface coating of the Ti3Al nanoparticles is a mixture of Al2O3 and TiO2. The production rate of Ti3Al nanoparticles was estimated to be about 3 g/h. This method has a great potential in mass production of Ti3Al nanoparticles.

  9. Continuous Flow Controlled Synthesis of Gold Nanoparticles Using Pulsed Mixing Microfluidic System

    Directory of Open Access Journals (Sweden)

    Guojun Liu

    2015-01-01

    Full Text Available To prepare the gold nanoparticles (AuNPs with uniform sizes, fine morphology, and good monodispersity, a pulsed mixing microfluidic system based on PZT actuation was presented. The system includes PZT micropump and Y type micromixer. By adjusting voltage (entrance flow rate, pulsed frequency, phase, and other parameters, a variety of mixing modes can be achieved, so as to realize the controllable synthesis of nanoparticles in a certain range. By numerical simulation and analysis, the channel section size, entrance angle, and pulse frequency were optimized. Based on the optimized structure and working parameters, the test prototype has been manufactured in lab, and the related synthesis tests of AuNPs were carried out. The test results indicate that AuNPs with uniform morphology and good monodispersity can be synthesized using the system with the section size (0.4 mm × 0.4 mm, the entrance channel angle (60° under condition of the pulsed frequency (300 Hz, and the entrance flow rate (4 mL/min. The average diameter and its standard deviation of AuNPs synthesized were 21.6 nm, 4.83 nm, respectively. The research work above can be applied to the fields such as the controlled synthesis of noble metal nanoparticles, biomedicine, and microchemical system.

  10. Saccharide-based Approach to Green Metallic Nanostructure Synthesis

    DEFF Research Database (Denmark)

    Engelbrekt, Christian; Sørensen, Karsten Holm; Jensen, Palle Skovhus;

    A green approach to solution synthesis of metallic nanoparticles has been developed using harmless and bioapplicable chemicals as well as moderate temperatures. Metal precursors are reduced by glucose/buffers and sterically stabilized by starch. The saccharide based procedure is highly diverse pr...

  11. Catharanthus roseus:a natural source for the synthesis of silver nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Mukunthan KS; Elumalai EK; Trupti N Patel; V Ramachandra Murty

    2011-01-01

    Objective: To develop a simple rapid procedure for bioreduction of silver nanoparticles (AgNPs) using aqueous leaves extracts of Catharanthus roseus (C. roseus). Methods: Characterization were determined by using UV-Vis spectrophotometry, scanning electron microscopy (SEM), energy dispersive X-ray and X-ray diffraction. Results: SEM showed the formation of silver nanoparticles with an average size of 67 nm to 48 nm. X-ray diffraction analysis showed that the particles were crystalline in nature with face centered cubic geometry. Conclusions: C. roseus demonstrates strong potential for synthesis of silver nanoparticles by rapid reduction of silver ions (Ag+ to Ag0). This study provides evidence for developing large scale commercial production of value-added products for biomedical/nanotechnology-based industries.

  12. Catharanthus roseus: a natural source for the synthesis of silver nanoparticles

    Science.gov (United States)

    Mukunthan, KS; Elumalai, EK; Patel, Trupti N; Murty, V Ramachandra

    2011-01-01

    Objective To develop a simple rapid procedure for bioreduction of silver nanoparticles (AgNPs) using aqueous leaves extracts of Catharanthus roseus (C. roseus). Methods Characterization were determined by using UV-Vis spectrophotometry, scanning electron microscopy (SEM), energy dispersive X-ray and X-ray diffraction. Results SEM showed the formation of silver nanoparticles with an average size of 67 nm to 48 nm. X-ray diffraction analysis showed that the particles were crystalline in nature with face centered cubic geometry. Conclusions C. roseus demonstrates strong potential for synthesis of silver nanoparticles by rapid reduction of silver ions (Ag+ to Ag0). This study provides evidence for developing large scale commercial production of value-added products for biomedical/nanotechnology-based industries. PMID:23569773

  13. SYNTHESIS AND APPLICATION OF NANOPARTICLES BY A HIGH GRAVITY METHOD

    Institute of Scientific and Technical Information of China (English)

    Lei Shao; Jianfeng Chen

    2005-01-01

    Fast chemical reactions involved in nanomaterials synthesis, polymerization, special chemicals production, reactive absorption, etc., are often difficult to control in terms of product quality, process efficiency and production consistency.After a theoretical analysis on such processes based on chemical reaction engineering fundamentals, an idea to intensify micromixing (mixing on the molecular scale) and mass transfer and therefore to control the process ideally was proposed.By experimental investigations of mass transfer and micromixing characteristics in the Rotating Packed Bed (RPB, or "HIGEE" device), we achieved unique intense micromixing. This led us to the invention of using RPB as a reactor for the fabrication of nanoparticles (Chen et al., 2000).RPB consists mainly of a rotating packed rotator inside a stationary casing. The high gravity environment created by the RPB, which could be orders of magnitude larger than gravity, causes aqueous reactants going through the packing to spread or split into micro or nano droplets, threads or thin films, thus markedly intensifying mass transfer and micromixing to the extent of 1 to 3 orders of magnitude larger than that in a conventional packed bed.In 1994, the first RPB reactor was designed to synthesize nanoparticles of CaCO3 through multiphase reaction between Ca(OH)2 slurry and CO2 gas, and nanoparticles of 15~30nm in mean size and with very uniform particle size distribution was obtained. In 1997, a pilot-scale RPB reactor was successfully set up for operation, and in 2000, the first commercial-scale RPB reactor for synthesis of such nanoparticles came into operation in China, establishing a milestone in the use of RPB as a reactor for the fabrication of nanomaterials (Chen et al., 2002).Since then, the high gravity method has been employed for the synthesis of inorganic and organic nanoparticles via gas-liquid, liquid-liquid, and gas-liquid-solid multiphase reactions, e.g. inorganic nanoparticles like

  14. Synthesis and properties MFe2O4 (M = Fe, Co) nanoparticles and core-shell structures

    Science.gov (United States)

    Yelenich, O. V.; Solopan, S. O.; Greneche, J. M.; Belous, A. G.

    2015-08-01

    Individual Fe3-xO4 and CoFe2O4 nanoparticles, as well as Fe3-xO4/CoFe2O4 core/shell structures were synthesized by the method of co-precipitation from diethylene glycol solutions. Core/shell structure were synthesized with CoFe2O4-shell thickness of 1.0, 2.5 and 3.5 nm. X-ray diffraction patterns of individual nanoparticles and core/shell are similar and indicate that all synthesized samples have a cubic spinel structure. Compares Mössbauer studies of CoFe2O4, Fe3-xO4 nanoparticles indicate superparamagnetic properties at 300 K. It was shown that individual magnetite nanoparticles are transformed into maghemite through oxidation during the synthesis procedure, wherein the smallest nanoparticles are completely oxidized while a magnetite core does occur in the case of the largest nanoparticles. The Mössbauer spectra of core/shell nanoparticles with increasing CoFe2O4-shell thickness show a gradual decrease in the relative intensity of the quadrupole doublet and significant decrease of the mean isomer shift value at both RT and 77 K indicating a decrease of the superparamagnetic relaxation phenomena. Specific loss power for the prepared ferrofluids was experimentally calculated and it was determined that under influence of ac-magnetic field magnetic fluid based on individual CoFe2O4 and Fe3-xO4 particles are characterized by very low heating temperature, when magnetic fluids based on core/shell nanoparticles demonstrate higher heating effect.

  15. Green synthesis of Silver nanoparticles through Calotropis gigantea leaf extracts and evaluation of antibacterial activity against Vibrio alginolyticus

    Directory of Open Access Journals (Sweden)

    Vaseeharan Baskaralingam

    2012-01-01

    Full Text Available Green synthesized silver nanoparticles by Calotropis gigantea leaf extract were used to study the inhibitory activity against pathogenic Vibrio alginolyticus, isolated from wild Artemia franciscana cysts. Silver nanoparticle synthesis was observed using UV-visible spectroscopy and the morphological characteristics were analyzed by atomic force microscope (AFM. In the present study, increasing concentrations of silver nanoparticles synthesized on LB agar plates effectively reduced the number of colonies of V. alginolyticus. A decrease in colonies (CFUs was observed at 5 mg/mL of silver nanoparticle concentration and the complete inhibition of V. alginolyticus was observed at 20 mg/mL of silver nanoparticle concentration on LB agar plates. In vivo controlling efficiency of silver nanoparticles was tested in an A. franciscana hatching system. Effective control of V. alginolyticus in brine shrimp A. franciscana hatching units was achieved by experimental infection and treatment with silver nanoparticles. Experimental infection studies showed that V. alginolyticus infected Artemia nauplii treated with silver nanoparticles (10 mg/mL had greater survival (>40% than silver nanoparticles not treated with nauplii. Based on the findings of this study, it is recommended that low concentrations of green synthesized silver nanoparticles should be further investigated for other potential experimental models to control potential medical pathogens.

  16. Synthesis of Carbon Encapsulated Mono- and Multi-Iron Nanoparticles

    Directory of Open Access Journals (Sweden)

    M. Reza Sanaee

    2015-01-01

    Full Text Available Core–shell nanostructures of carbon encapsulated iron nanoparticles (CEINPs show unique properties and technological applications, because carbon shell provides extreme chemical stability and protects pure iron core against oxidation without impairing the possibility of functionalization of the carbon surface. Enhancing iron core magnetic properties and, in parallel, improving carbon shell sealing are the two major challenges in the synthesis of CEINPs. Here, we present the synthesis of both CEINPs and a new carbon encapsulated multi-iron nanoparticle by a new modified arc discharge reactor. The nanoparticle size, composition, and crystallinity and the magnetic properties have been studied. The morphological properties were observed by scanning electron microscopy and transmission electron microscopy. In order to evaluate carbon shell protection, the iron cores were characterized by selected area diffraction and fast Fourier transform techniques as well as by electron energy loss and energy dispersive X-ray spectroscopies. Afterward, the magnetic properties were investigated using a superconducting quantum interference device. As main results, spherical, oval, and multi-iron cores were controllably synthesized by this new modified arc discharge method. The carbon shell with high crystallinity exhibited sufficient protection against oxidation of pure iron cores. The presented results also provided new elements for understanding the growth mechanism of iron core and carbon shell.

  17. Facile Synthesis of Calcium Carbonate Nanoparticles from Cockle Shells

    Directory of Open Access Journals (Sweden)

    Kh. Nurul Islam

    2012-01-01

    Full Text Available A simple and low-cost method for the synthesis of calcium carbonate nanoparticles from cockle shells was described. Polymorphically, the synthesized nanoparticles were aragonites which are biocompatible and thus frequently used in the repair of fractured bone and development of advanced drug delivery systems, tissue scaffolds and anticarcinogenic drugs. The rod-shaped and pure aragonite particles of 30±5 nm in diameter were reproducibly synthesized when micron-sized cockle shells powders were mechanically stirred for 90 min at room temperature in presence of a nontoxic and nonhazardous biomineralization catalyst, dodecyl dimethyl betaine (BS-12. The findings were verified using a combination of analytical techniques such as variable pressure scanning electron microscopy (VPSEM, transmission electron microscopy (TEM, Fourier transmission infrared spectroscopy (FT-IR, X-ray diffraction spectroscopy (XRD, and energy dispersive X-ray analyser (EDX. The reproducibility and low cost of the method suggested that it could be used in industry for the large scale synthesis of aragonite nanoparticles from cockle shells, a low cost and easily available natural resource.

  18. Effective biological dose from occupational exposure during nanoparticle synthesis

    International Nuclear Information System (INIS)

    Nanomaterial and nanotechnology safety require the characterization of occupational exposure levels for completing a risk assessment. However, equally important is the estimation of the effective internal dose via lung deposition, transport and clearance mechanisms. An integrated source-to-biological dose assessment study is presented using real monitoring data collected during nanoparticle synthesis. Experimental monitoring data of airborne exposure levels during nanoparticle synthesis of CaSO4 and BiPO4 nanoparticles in a research laboratory is coupled with a human lung transport and deposition model, which solves in an Eulerian framework the general dynamic equation for polydisperse aerosols using particle specific physical-chemical properties. Subsequently, the lung deposition model is coupled with a mathematical particle clearance model providing the effective biological dose as well as the time course of the biological dose build-up after exposure. The results for the example of BiPO4 demonstrate that even short exposures throughout the day can lead to particle doses of 1.10·E+08/(kg-bw·8h-shift), with the majority accumulating in the pulmonary region. Clearance of particles is slow and is not completed within a working shift following a 1 hour exposure. It mostly occurs via macrophage activity in the alveolar region, with small amounts transported to the interstitium and less to the lymph nodes.

  19. Effective biological dose from occupational exposure during nanoparticle synthesis

    Science.gov (United States)

    Demou, Evangelia; Tran, Lang; Housiadas, Christos

    2009-02-01

    Nanomaterial and nanotechnology safety require the characterization of occupational exposure levels for completing a risk assessment. However, equally important is the estimation of the effective internal dose via lung deposition, transport and clearance mechanisms. An integrated source-to-biological dose assessment study is presented using real monitoring data collected during nanoparticle synthesis. Experimental monitoring data of airborne exposure levels during nanoparticle synthesis of CaSO4 and BiPO4 nanoparticles in a research laboratory is coupled with a human lung transport and deposition model, which solves in an Eulerian framework the general dynamic equation for polydisperse aerosols using particle specific physical-chemical properties. Subsequently, the lung deposition model is coupled with a mathematical particle clearance model providing the effective biological dose as well as the time course of the biological dose build-up after exposure. The results for the example of BiPO4 demonstrate that even short exposures throughout the day can lead to particle doses of 1.10·E+08#/(kg-bw·8h-shift), with the majority accumulating in the pulmonary region. Clearance of particles is slow and is not completed within a working shift following a 1 hour exposure. It mostly occurs via macrophage activity in the alveolar region, with small amounts transported to the interstitium and less to the lymph nodes.

  20. Green synthesis of nanoparticles: Their advantages and disadvantages

    Science.gov (United States)

    Parveen, Khadeeja; Banse, Viktoria; Ledwani, Lalita

    2016-04-01

    The nanotechnology and biomedical sciences opens the possibility for a wide variety of biological research topics and medical uses at the molecular and cellular level. The biosynthesis of nanoparticles has been proposed as a cost-effective and environmentally friendly alternative to chemical and physical methods. Plant-mediated synthesis of nanoparticles is a green chemistry approach that connects nanotechnology with plants. Novel methods of ideally synthesizing NPs are thus thought that are formed at ambient temperatures, neutral pH, low costs and environmentally friendly fashion. Keeping these goals in view nanomaterials have been synthesized using various routes. Among the biological alternatives, plants and plant extracts seem to be the best option. Plants are nature's "chemical factories". They are cost efficient and require low maintenance. The advantages and disadvantages of nanotechnology can be easily enumerated. This study attempts to review the diversity of the field, starting with the history of nanotechnology, the properties of the nanoparticle, various strategies of synthesis, the many advantages and disadvantages of different methods and its application.

  1. Sonochemical synthesis of magnetic Janus nanoparticles.

    Science.gov (United States)

    Teo, Boon M; Suh, Su Kyung; Hatton, T Alan; Ashokkumar, Muthupandian; Grieser, Franz

    2011-01-01

    The sonochemical synthesis of nanosized surface-dissymmetrical (Janus) particles is described. The Janus particles were composed of silica and polystyrene, with the polystyrene portion loaded with nanosized magnetite particles. It is shown that the Janus particles can be used to form kinetically stable oil-in-water emulsions that can be spontaneously broken on application of an external magnetic field. The one-pot synthetic process used to prepare the Janus particles has several advantages over other conventional methods of producing such particles. PMID:21133341

  2. Synthesis and Characterization of Chromium Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    Vivek Sheel Jaswal

    2014-06-01

    Full Text Available Chromium oxide nanoparticles (NPshave been rapidly synthesized by precipitation method using ammomia as precipitating agent and are characterized by using X-ray Diffraction (XRD, Thermo Gravimetric Analysis (TGA, UV-Visible absorption (UV, Infrared Spectoscopy (IR, Scanning Electron Microscopy (SEM and Transmission Electron Microscopy (TEM. XRD studies show that chromium oxide NP is formed as Cr2O3 and it has hexagonal structure. The shape and particle size of the synthesized Cr2O3 NPs is determined by SEM and TEM. The images showed that the size of NPs of Cr2O3 varied from 20 nm to 70 nm with average crystalline size 45 nm. UV-Visible absorption and IR spectoscopy confirm the formation of nanosized Cr2O3. TGA verifies that the Cr2O3 NPs are thermally stable upto 1000 °C.

  3. Hydrothermal synthesis, off-axis electron holography and magnetic properties of Fe3O4 nanoparticles

    DEFF Research Database (Denmark)

    Almeida, Trevor P.; Muxworthy, Adrian R.; Williams, Wyn;

    2014-01-01

    The hydrothermal synthesis of Fe3O4 nanoparticles (NPs) (<50 nm) from mixed FeCl3 / FeCl2 precursor solution at pH ~ 12 has been confirmed using complementary characterisation techniques of transmission electron microscopy and X-ray diffractometry. Off-axis electron holography allowed for visuali......The hydrothermal synthesis of Fe3O4 nanoparticles (NPs) (

  4. Gold Nanoparticles as the Catalyst of Single-Walled Carbon Nanotube Synthesis

    Directory of Open Access Journals (Sweden)

    Yoshikazu Homma

    2014-03-01

    Full Text Available Gold nanoparticles have been proven to act as efficient catalysts for chemical reactions, such as oxidation and hydrogen production. In this review we focus on a different aspect of the catalysis of gold nanoparticles; single-walled carbon nanotube (SWCNT synthesis. This is not a traditional meaning of catalytic reaction, but SWCNTs cannot be synthesized without nanoparticles. Previously, gold was considered as unsuitable metal species as the catalyst of SWCNT synthesis. However, gold nanoparticles with diameters smaller than 5 nm were found to effectively produce SWCNTs. We discuss the catalysis of gold and related metals for SWCNT synthesis in comparison with conventional catalysts, such as iron, cobalt, and nickel.

  5. High-Yield Synthesis and Applications of Anisotropic Gold Nanoparticles

    Science.gov (United States)

    Vigderman, Leonid

    This work will describe research directed towards the synthesis of anisotropic gold nanoparticles as well as their functionalization and biological applications. The thesis will begin by describing a new technique for the high-yield synthesis of gold nanorods using hydroquinone as a reducing agent. This addresses important limitations of the traditional nanorod synthesis including low yield of gold ions conversion to metallic form and inability to produce rods with longitudinal surface plasmon peak above 850 nm. The use of hydroquinone was also found to improve the synthesis of gold nanowires via the nanorod-seed mediated procedure developed in our lab. The thesis will next present the synthesis of novel starfruitshaped nanorods, mesorods, and nanowires using a modified nanorod-seed mediated procedure. The starfruit particles displayed increased activity as surfaceenhanced Raman spectroscopy (SERS) substrates as compared to smooth structures. Next, a method for the functionalization of gold nanorods using a cationic thiol, 16-mercaptohexadecyltrimethylammonium bromide (MTAB), will be described. By using this thiol, we were able to demonstrate the complete removal of toxic surfactant from the nanorods and were also able to precisely quantify the grafting density of thiol molecules on the nanorod surface through a combination of several analytical techniques. Finally, this thesis will show that MTABfunctionalized nanorods are nontoxic and can be taken up in extremely high numbers into cancer cells. The thesis will conclude by describing the surprising uptake of larger mesorods and nanowires functionalized with MTAB into cells in high quantities.

  6. Synthesis, characterization and mechanistic insights of mycogenic iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bhargava, Arpit; Jain, Navin; Manju Barathi L [Birla Institute of Technology and Science, Centre for Biotechnology, Department of Biological Sciences (India); Akhtar, Mohd Sayeed [Jimma University, Department of Applied Microbiology, College of Natural Sciences (Ethiopia); Yun, Yeoung-Sang [Chonbuk National University, Division of Environmental and Chemical Engineering (Korea, Republic of); Panwar, Jitendra, E-mail: drjitendrapanwar@yahoo.co.in [Birla Institute of Technology and Science, Centre for Biotechnology, Department of Biological Sciences (India)

    2013-11-15

    In the present study, extracellular synthesis of iron oxide nanoparticles (IONPs) was achieved using Aspergillus japonicus isolate AJP01. The isolate demonstrated its ability to hydrolyze the precursor salt solution, a mixture of iron cyanide complexes, under ambient conditions. Hydrolysis of these complexes released ferric and ferrous ions, which underwent protein-mediated coprecipitation and controlled nucleation resulting in the formation of IONPs. Transmission electron microscopy, selected area electron diffraction pattern, energy dispersive spectroscopy and grazing incidence X-ray diffraction analysis confirmed the mycosynthesis of IONPs. The synthesized particles were cubic in shape with a size range of 60–70 nm with crystal structure corresponding to magnetite. Scanning electron microscopy analysis revealed the absence of IONPs on fungal biomass surface, indicating the extracellular nature of synthesis. Fourier transform infrared spectroscopy confirmed the presence of proteins on as-synthesised IONPs, which may confer their stability. Preliminary investigation indicated the role of proteins in the synthesis and stabilization of IONPs. On the basis of present findings, a probable mechanism for synthesis of IONPs is suggested. The simplicity and versatility of the present approach can be utilized for the synthesis of other nanomaterials.

  7. Synthesis of ZnO nanoparticles using surfactant free in-air and microwave method

    International Nuclear Information System (INIS)

    Zinc oxide nanoparticles have been successfully prepared by a facile route involving the reaction of zinc sulphate heptahydrate and sodium hydroxide through drop-by-drop mixing synthesis-IA, instant mixing synthesis-IA and under the influence of microwave radiations. The synthesis under different reaction conditions played an important role and led to the formation of zinc oxide nanoparticles of different size and shapes. The synthesized nanoparticles were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM) techniques. The concentration dependent antimicrobial activity of synthesized ZnO nanoparticles was carried out. The photocatalytic activity was evaluated using the photodegradation of methylene blue (MB) dye under UV irradiation. Further, the optical properties of as-prepared ZnO nanoparticles were investigated by UV-vis spectrophotometry. The absence of surfactant led to a simple, cheap and fast method of synthesis of zinc oxide nanoparticles.

  8. Seed mediated synthesis of highly mono-dispersed gold nanoparticles in the presence of hydroquinone

    Science.gov (United States)

    Kumar, Dhiraj; Mutreja, Isha; Sykes, Peter

    2016-09-01

    Gold nanoparticles (AuNPs) are being studied for several biomedical applications, including drug delivery, biomedical imaging, contrast agents and tumor targeting. The synthesis of nanoparticles with a narrow size distribution is critical for these applications. We report the synthesis of highly mono-dispersed AuNPs by a seed mediated approach, in the presence of tri-sodium citrate and hydroquinone (HQ). AuNPs with an average size of 18 nm were used for the synthesis of highly mono-dispersed nanocrystals of an average size 40 nm, 60 nm, 80 nm and ∼100 nm; but the protocol is not limited to these sizes. The colloidal gold was subjected to UV–vis absorbance spectroscopy, showing a red shift in lambda max wavelength, peaks at 518.47 nm, 526.37 nm, 535.73 nm, 546.03 nm and 556.50 nm for AuNPs seed (18 nm), 40 nm, 60 nm, 80 nm and ∼100 nm respectively. The analysis was consistent with dynamic light scattering and electron microscopy. Hydrodynamic diameters measured were 17.6 nm, 40.8 nm, 59.8 nm, 74.1 nm, and 91.4 nm (size by dynamic light scattering—volume %); with an average poly dispersity index value of 0.088, suggesting mono-dispersity in the size distribution, which was also confirmed by transmission electron microscopy analysis. The advantage of a seed mediated approach is a multi-step growth of nanoparticle size that enables us to control the number of nanoparticles in the suspension, for size ranging from 24.5 nm to 95.8 nm. In addition, the HQ-based synthesis of colloidal nanocrystals allowed control of the particle size and size distribution by tailoring either the number of seeds, amount of gold precursor or reducing agent (HQ) in the final reaction mixture.

  9. Seed mediated synthesis of highly mono-dispersed gold nanoparticles in the presence of hydroquinone

    Science.gov (United States)

    Kumar, Dhiraj; Mutreja, Isha; Sykes, Peter

    2016-09-01

    Gold nanoparticles (AuNPs) are being studied for several biomedical applications, including drug delivery, biomedical imaging, contrast agents and tumor targeting. The synthesis of nanoparticles with a narrow size distribution is critical for these applications. We report the synthesis of highly mono-dispersed AuNPs by a seed mediated approach, in the presence of tri-sodium citrate and hydroquinone (HQ). AuNPs with an average size of 18 nm were used for the synthesis of highly mono-dispersed nanocrystals of an average size 40 nm, 60 nm, 80 nm and ˜100 nm; but the protocol is not limited to these sizes. The colloidal gold was subjected to UV-vis absorbance spectroscopy, showing a red shift in lambda max wavelength, peaks at 518.47 nm, 526.37 nm, 535.73 nm, 546.03 nm and 556.50 nm for AuNPs seed (18 nm), 40 nm, 60 nm, 80 nm and ˜100 nm respectively. The analysis was consistent with dynamic light scattering and electron microscopy. Hydrodynamic diameters measured were 17.6 nm, 40.8 nm, 59.8 nm, 74.1 nm, and 91.4 nm (size by dynamic light scattering—volume %); with an average poly dispersity index value of 0.088, suggesting mono-dispersity in the size distribution, which was also confirmed by transmission electron microscopy analysis. The advantage of a seed mediated approach is a multi-step growth of nanoparticle size that enables us to control the number of nanoparticles in the suspension, for size ranging from 24.5 nm to 95.8 nm. In addition, the HQ-based synthesis of colloidal nanocrystals allowed control of the particle size and size distribution by tailoring either the number of seeds, amount of gold precursor or reducing agent (HQ) in the final reaction mixture.

  10. Synthesis and characterization of magnetite nanoparticles from mineral magnetite

    Energy Technology Data Exchange (ETDEWEB)

    Morel, Mauricio, E-mail: mmorel@ing.uchile.cl [Laboratorio de Síntesis y Polímeros, Departamento de ciencias de los Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Santiago (Chile); Laboratorio de Materiales a Nanoescala, Departamento de ciencias de los Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Avenue Tupper 2069, Santiago (Chile); Martínez, Francisco, E-mail: polimart@ing.uchile.cl [Laboratorio de Síntesis y Polímeros, Departamento de ciencias de los Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Santiago (Chile); Mosquera, Edgar [Laboratorio de Materiales a Nanoescala, Departamento de ciencias de los Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Avenue Tupper 2069, Santiago (Chile)

    2013-10-15

    We have synthesized magnetite nanoparticles with sizes that range from 20 to 30 nm from mineral magnetite roughly 45 μm in size. The procedure consists in the dissolution of the mineral in an acidic medium and subsequent precipitation in a basic medium in the presence of oleic acid. Two experiments were conducted in different gaseous environments. The first was carried out in an environment exposed to air (M1) and the second in an N{sub 2} (M2) environment. The x-ray diffraction results showed a slight difference, which corresponds to the surface oxidation of magnetite. The sizes of the modified nanoparticles were determined through the Scherrer equation and transmission electron microscopy. An organic material mass loss corresponding to 18% was observed through a thermogravimetric analysis. The Fourier transform infrared spectroscopic analysis provides information about the type of bond that is formed on the surface of the nanoparticle, which corresponds to a bidentate chelate. The vibrating sample magnetometer results show a superparamagnetic behavior for sample M1. - Highlights: • A new method for synthesis of nanoparticles from mineral microparticles. • Search agreggate value to the mineral by mean nanoscience. • The stoichiometric ratio of the ions Fe{sup 2+} and Fe{sup 3+} from the mineral magnetite is synergistic.

  11. Synthesis and characterization of magnetite nanoparticles from mineral magnetite

    International Nuclear Information System (INIS)

    We have synthesized magnetite nanoparticles with sizes that range from 20 to 30 nm from mineral magnetite roughly 45 μm in size. The procedure consists in the dissolution of the mineral in an acidic medium and subsequent precipitation in a basic medium in the presence of oleic acid. Two experiments were conducted in different gaseous environments. The first was carried out in an environment exposed to air (M1) and the second in an N2 (M2) environment. The x-ray diffraction results showed a slight difference, which corresponds to the surface oxidation of magnetite. The sizes of the modified nanoparticles were determined through the Scherrer equation and transmission electron microscopy. An organic material mass loss corresponding to 18% was observed through a thermogravimetric analysis. The Fourier transform infrared spectroscopic analysis provides information about the type of bond that is formed on the surface of the nanoparticle, which corresponds to a bidentate chelate. The vibrating sample magnetometer results show a superparamagnetic behavior for sample M1. - Highlights: • A new method for synthesis of nanoparticles from mineral microparticles. • Search agreggate value to the mineral by mean nanoscience. • The stoichiometric ratio of the ions Fe2+ and Fe3+ from the mineral magnetite is synergistic

  12. Immobilization of bacterial S-layer proteins from Caulobacter crescentus on iron oxide-based nanocomposite: synthesis and spectroscopic characterization of zincite-coated Fe₂O₃ nanoparticles.

    Science.gov (United States)

    Habibi, Neda

    2014-05-01

    Zinc oxide was coated on Fe2O3 nanoparticles using sol-gel spin-coating. Caulobacter crescentus have a crystalline surface layer (S-layer), which consist of one protein or glycoprotein species. The immobilization of bacterial S-layers obtained from C. crescentus on zincite-coated nanoparticles of iron oxide was investigated. The SDS PAGE results of S-layers isolated from C. crescentus showed the weight of 50 KDa. Nanoparticles of the Fe2O3 and zinc oxide were synthesized by a sol-gel technique. Fe2O3 nanoparticles with an average size of 50 nm were successfully prepared by the proper deposition of zinc oxide onto iron oxide nanoparticles surface annealed at 450 °C. The samples were characterized by field-emission scanning electron microscope (FESEM), atomic force microscopy (AFM), powder X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FT-IR).

  13. Gold Nanoparticles as the Catalyst of Single-Walled Carbon Nanotube Synthesis

    OpenAIRE

    Yoshikazu Homma

    2014-01-01

    Gold nanoparticles have been proven to act as efficient catalysts for chemical reactions, such as oxidation and hydrogen production. In this review we focus on a different aspect of the catalysis of gold nanoparticles; single-walled carbon nanotube (SWCNT) synthesis. This is not a traditional meaning of catalytic reaction, but SWCNTs cannot be synthesized without nanoparticles. Previously, gold was considered as unsuitable metal species as the catalyst of SWCNT synthesis. However, gold nanopa...

  14. First Synthesis of Uranyl Aluminate nano-particles

    Energy Technology Data Exchange (ETDEWEB)

    Chave, T.; Nikitenko, S. I. [UMII, ICSM, CEA, CNRS, ENSCM, Ctr Marcoule, UMR 5257, F-30207 Bagnols Sur Ceze (France); Scheinost, A. C. [European Synchrotron Radiat Facil, Rossendorf Beamline CRG BM20, F-38043 Grenoble (France); Scheinost, A. C. [FZD, Inst Radiochem, D-01314 Dresden (Germany); Berthon, C.; Arab-Chapelet, B.; Moisy, Ph. [CEA Marcoule, DEN, DRCP, Ctr Marcoule, F-30207 Bagnols Sur Ceze (France)

    2010-07-01

    This paper describes, for the first time, a simple method for the synthesis of uranyl aluminate (URAL) nano-particles. URAL was prepared by U(VI) hydrolytic precipitation with ammonia at pH = 11 in the presence of meso-porous alumina MSU-X under 20 kHz of sonication followed by annealing of the obtained solids at 800 C. TEM, XAFS, powder XRD, and {sup 27}Al MAS NMR studies revealed that the speciation of uranium in this system strongly depends on uranium concentration. The sample with 5 wt % of uranium yields air-stable nano-particles (similar to 5 nm) of URAL. Presumably, UO{sub 2}{sup 2+} cations in this compound are coordinated with bidentate AlO{sub 2}{sup -} groups. The increase of uranium concentration to 30 wt % causes mostly formation of U{sub 3}O{sub 8} fine particles (similar to 50 nm) and small amounts of URAL. (authors)

  15. First Synthesis of Uranyl Aluminate nano-particles

    International Nuclear Information System (INIS)

    This paper describes, for the first time, a simple method for the synthesis of uranyl aluminate (URAL) nano-particles. URAL was prepared by U(VI) hydrolytic precipitation with ammonia at pH = 11 in the presence of meso-porous alumina MSU-X under 20 kHz of sonication followed by annealing of the obtained solids at 800 C. TEM, XAFS, powder XRD, and 27Al MAS NMR studies revealed that the speciation of uranium in this system strongly depends on uranium concentration. The sample with 5 wt % of uranium yields air-stable nano-particles (similar to 5 nm) of URAL. Presumably, UO22+ cations in this compound are coordinated with bidentate AlO2- groups. The increase of uranium concentration to 30 wt % causes mostly formation of U3O8 fine particles (similar to 50 nm) and small amounts of URAL. (authors)

  16. Synthesis and properties of magnetic ceramic nanoparticles

    Science.gov (United States)

    Sorescu, Monica

    2012-02-01

    Magnetic ceramic nanoparticles of the type xIn2O3-(1-x)alpha-Fe2O3, xV2O5-(1-x)alpha-Fe2O3 and xZnO-(1-x)alpha-Fe2O3 (x=0.1-0.7) were synthesized from the mixed oxides using mechanochemical activation for 0-12 hours. X-ray diffraction was used to derive the phase content, lattice constants and particle size information as function of ball milling time. Mossbauer spectroscopy results correlated with In3+, V5+ and Zn2+ substitution of Fe3+ in the hematite lattice. SEM/EDS measurements revealed that the mechanochemical activation by ball milling produced systems with a wide range of particle size distribution, from nanometer particles to micrometer agglomerates, but with a uniform distribution of the elements. Simultaneous DSC-TGA investigations up to 800 degrees C provided information on the heat flow, weight loss and the enthalpy of transformation in the systems under investigation. This study demonstrates the formation of a nanostructured solid solution for the indium oxide, an iron vanadate (FeVO4) for the vanadium oxide, and of the zinc ferrite (ZnFe2O4) for the zinc oxide. The transformation pathway for each case can be related to the oxidation state of the metallic specie of the oxide used in connection with hematite.

  17. Synthesis of tungsten oxide, silver, and gold nanoparticles by radio frequency plasma in water

    International Nuclear Information System (INIS)

    Highlights: •RF plasma in water was used for nanoparticle synthesis. •Nanoparticles were produced from erosion of metallic electrode. •Rectangular and spherical tungsten oxide nanoparticles were produced. •No oxidations of the silver and gold spherical nanoparticles were produced. -- Abstract: A process for synthesis of nanoparticles using plasma in water generated by a radio frequency of 27.12 MHz is proposed. Tungsten oxide, silver, and gold nanoparticles were produced at 20 kPa through erosion of a metallic electrode exposed to plasma. Characterization of the produced nanoparticles was carried out by XRD, absorption spectrum, and TEM. The nanoparticle sizes were compared with those produced by a similar technique using plasma in liquid

  18. Green synthesis of silver nanoparticles mediated by Pulicaria glutinosa extract

    Directory of Open Access Journals (Sweden)

    Khan M

    2013-04-01

    Full Text Available Mujeeb Khan,1 Merajuddin Khan,1 Syed Farooq Adil,1 Muhammad Nawaz Tahir,2 Wolfgang Tremel,2 Hamad Z Alkhathlan,1 Abdulrahman Al-Warthan,1 Mohammed Rafiq H Siddiqui1 1Department of Chemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia; 2Institute of Inorganic and Analytical Chemistry, Johannes Gutenberg-University of Mainz, Mainz, Germany Abstract: The green synthesis of metallic nanoparticles (NPs has attracted tremendous attention in recent years because these protocols are low cost and more environmentally friendly than standard methods of synthesis. In this article, we report a simple and eco-friendly method for the synthesis of silver NPs using an aqueous solution of Pulicaria glutinosa plant extract as a bioreductant. The as-prepared silver NPs were characterized using ultraviolet–visible spectroscopy, powder X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier-transform infrared spectroscopy. Moreover, the effects of the concentration of the reductant (plant extract and precursor solution (silver nitrate, the temperature on the morphology, and the kinetics of reaction were investigated. The results indicate that the size of the silver NPs varied as the plant extract concentration increased. The as-synthesized silver NPs were phase pure and well crystalline with a face-centered cubic structure. Further, Fourier-transform infrared spectroscopy analysis confirmed that the plant extract not only acted as a bioreductant but also functionalized the NPs' surfaces to act as a capping ligand to stabilize them in the solvent. The developed eco-friendly method for the synthesis of NPs could prove a better substitute for the physical and chemical methods currently used to prepare metallic NPs commonly used in cosmetics, foods, and medicines. Keywords: surface plasmon resonance, metallic nanoparticles, eco-friendly, capping ligand

  19. Calix-Based Nanoparticles: A Review.

    Science.gov (United States)

    Kongor, Anita R; Mehta, Viren A; Modi, Krunal M; Panchal, Manthan K; Dey, Shuvankar A; Panchal, Urvi S; Jain, Vinod K

    2016-06-01

    Calixarenes are considered as third generation supramolecules with hollow cavity-like architecture whereas nanoparticles are small entities with dimensions in the nanoscale. Many exciting achievements are seen when the calix system merges with nanoparticles which produces many fascinating facets in all fields of contemporary chemistry. The properties of nanoparticles which are tuned by calixarenes find applications in sensing, catalysis, molecular recognition, etc. Here, we have reviewed the chemistry of calix-based nanoparticles, and emphasis is laid on the modified, reducing, templated and stabilizing roles of calixarenes. This review covers the research being carried out in the domain of calix protected metal nanoparticles during last 18 years under the canopy of important 109 references. This article contains 58 figures which include 81 easy to understand structures. Calix-protected nanoparticles have enthralled researchers in the field of nanoscience with a tremendous growth in its applications, which heralds much promise to become in future a separate area of research. PMID:27573268

  20. PHYTO-ASSISTED SYNTHESIS AND CHARACTERIZATION OF SILVER NANOPARTICLES FROM AMARANTHUS DUBIUS

    OpenAIRE

    M. Jannathul Firdhouse; Lalitha, P.

    2012-01-01

    The aqueous extract of Amaranthus dubius was used for the green synthesis of silver nanoparticles from silver nitrate solution under various conditions. The silver nanoparticles were characterized by spectrophotometric, physical and theoretical methods. The size of silver nanoparticles ranged from 10-70nm. The present approach of biosynthesis of silver nanoparticles using aqueous extract of A.dubius appears to be cost efficient, eco-friendly and an easy alternative to conventional chemical me...

  1. Green synthesis of silver nanoparticles mediated by Pulicaria glutinosa extract.

    Science.gov (United States)

    Khan, Mujeeb; Khan, Merajuddin; Adil, Syed Farooq; Tahir, Muhammad Nawaz; Tremel, Wolfgang; Alkhathlan, Hamad Z; Al-Warthan, Abdulrahman; Siddiqui, Mohammed Rafiq H

    2013-01-01

    The green synthesis of metallic nanoparticles (NPs) has attracted tremendous attention in recent years because these protocols are low cost and more environmentally friendly than standard methods of synthesis. In this article, we report a simple and eco-friendly method for the synthesis of silver NPs using an aqueous solution of Pulicaria glutinosa plant extract as a bioreductant. The as-prepared silver NPs were characterized using ultraviolet-visible spectroscopy, powder X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier-transform infrared spectroscopy. Moreover, the effects of the concentration of the reductant (plant extract) and precursor solution (silver nitrate), the temperature on the morphology, and the kinetics of reaction were investigated. The results indicate that the size of the silver NPs varied as the plant extract concentration increased. The as-synthesized silver NPs were phase pure and well crystalline with a face-centered cubic structure. Further, Fourier-transform infrared spectroscopy analysis confirmed that the plant extract not only acted as a bioreductant but also functionalized the NPs' surfaces to act as a capping ligand to stabilize them in the solvent. The developed eco-friendly method for the synthesis of NPs could prove a better substitute for the physical and chemical methods currently used to prepare metallic NPs commonly used in cosmetics, foods, and medicines.

  2. Synthesis of Core/Shell MnFe{sub 2}O{sub 4}/Au Nanoparticles for Advanced Proton Treatment

    Energy Technology Data Exchange (ETDEWEB)

    Park, Jeong Chan [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2014-05-15

    Among many approaches for the surface modification with materials, such as polymers, organic ligands and metals, one of the most attractive ways is using metals. The fabrication of metal-based, monolayer-coated magnetic nanoparticles has been intensively studied. However, the synthesis of metal-capped magnetic nanoparticles with monodIspersities and controllable sizes is still challenged. Recently, gold-capped magnetic nanoparticles have been reported to increase stability and to provide biocompatibility. Magnetic nanoparticle with gold coating is an attractive system, which can be stabilized in biological conditions and readily functionalized through well-established surface modification (Au-S) chemistry. The Au coating offers plasmonic properties to magnetic nanoparticles. The core/shell nanoparticles were transferred from organic to aqueous solutions for biomedical applications. The core/shell structured MnFe{sub 2}O{sub 4}/Au nanoparticles have been prepared and transferred from organic phase to aqueous solutions. The resulting Au-coated nanocrystals may be an attractive system for biomedical applications, which are needed both magnetic resonance imaging and optical imaging. The phase transferred core/shell nanoparticles can be decorated with targeting moiety, such as antibodies, peptides, aptamers, small molecules and ligands for biological applications. The proton treatment with the resulting Au-MnFe{sub 2}O{sub 4} nanoparticles is undergoing.

  3. Controllable synthesis and sintering of silver nanoparticles for inkjet-printed flexible electronics

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Zhiliang, E-mail: zhzhl@iccas.ac.cn [Shandong Provincial Key Laboratory of Fine Chemicals, Qilu University of Technology, Jinan 250353 (China); Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China); Zhu, Weiyue [Shandong Provincial Key Laboratory of Fine Chemicals, Qilu University of Technology, Jinan 250353 (China)

    2015-11-15

    An effective and facile strategy was developed to successfully synthesize nearly uniform silver nanoparticles (AgNPs) with particle size of <10 nm, and demonstrated to achieve the sintering of AgNPs at room temperature for inkjet-printed flexible electronics. In such system, a series of different chain-length alkylamines were exploited as capped molecules to controllable synthesis of uniform AgNPs with the mean nanoparticle size in rang of 8.6 ± 0.9, 8.9 ± 1.2 and 9.2 ± 1.6 nm, and these ultra-small nanoparticles were very favorable to attain an excellent printing fluency. Based on the as-synthesized AgNPs, a sequence of flexible electrocircuits was successfully fabricated by ink-jet printing technique. After the dipped treatment, the printed AgNPs were achieved to spontaneous coalescence and aggregation at room temperature induced by preferential dissolution of capped molecules on AgNPs surfaces into methanol solution. These aggregated AgNPs demonstrated superior controllability, excellent stability and low resistivity in the range of 31.6–26.5 μΩ cm, and would have enormous potential in the application to be tailored for assembly of optoelectronics devices. - Highlights: • Silver nanoparticles with particle size of <10 nm was controllably synthesized. • The sintering of silver nanoparticles was conducted at room temperature. • The resistivity was reached as low as 26.5 μΩ cm for flexible electronics.

  4. In situ synthesis of polysaccharide nanoparticles via polyion complex of carboxymethyl cellulose and chitosan.

    Science.gov (United States)

    Kaihara, Sachiko; Suzuki, Yoichi; Fujimoto, Keiji

    2011-07-01

    Biocompatible polymer-magnetite hybrid nanoparticles were prepared by means of in situ synthesis of magnetite within polysaccharide hydrogel nanoparticles. Hydrogel nanoparticles were first fabricated by blending high-molecular-weight carboxymethyl cellulose as an anionic polymer, and low-molecular-weight chitosan as a cationic polymer to form polyion complexes (CC particles). These polyion complexes were then chemically crosslinked using genipin, a bio-based cross-linker, to form stable nanoparticles having a semi-IPN structure (CCG particles). Magnetite was lastly synthesized within CCG particles by the coprecipitation method to obtain polymer-magnetite hybrid nanoparticles (CCGM particles). The formations of CC, CCG and CCGM particles were mainly observed by transmittance, absorbance of genipin and TEM, respectively, and their hydrodynamic diameters and zeta-potentials were analyzed. It was confirmed that the hydrodynamic diameters and the zeta-potentials of these particles were significantly influenced by pH of the suspension, which was attributed to the charges of polymers. The diameters of CCGM particles were smaller than 200 nm at any pH conditions, suggesting the possibility to apply them as drug delivery carriers. CCGM particles exhibited the responsiveness to a magnetic field in addition to their high dispersion stability, indicating their potential to be utilized as a biomaterial for hyperthermia.

  5. Facile synthesis of magnetic-/pH-responsive hydrogel beads based on Fe3O4 nanoparticles and chitosan hydrogel as MTX carriers for controlled drug release.

    Science.gov (United States)

    Wu, Juan; Jiang, Wei; Tian, Renbing; Shen, Yewen; Jiang, Wei

    2016-10-01

    In the present study, methotrexate (MTX)-encapsulated magnetic-/pH-responsive hydrogel beads based on Fe3O4 nanoparticles and chitosan were successfully prepared through a one-step gelation process, which is a very facile, economic and environmentally friendly route. The developed hydrogel beads exhibited homogeneous porous structure and super-paramagnetic responsibility. MTX can be successfully encapsulated into magnetic chitosan hydrogel beads, and the drug encapsulation efficiency (%) and encapsulation content (%) were 93.8 and 6.28%, respectively. In addition, the drug release studies in vitro indicated that the MTX-encapsulated magnetic chitosan hydrogel beads had excellent pH-sensitivity, 90.6% MTX was released from the magnetic chitosan hydrogel beads within 48 h at pH 4.0. WST-1 assays in human liver hepatocellular carcinoma cells (HepG2) demonstrated that the MTX-encapsulated magnetic chitosan hydrogel beads had good cytocompatibility and high anti-tumor activity. Therefore, our results revealed that the MTX-encapsulated magnetic chitosan hydrogel beads would be a competitive candidate for controlled drug release in the area of targeted cancer therapy in the near future. PMID:27464586

  6. Cinnamomum tamala leaf extract-mediated green synthesis of Ag nanoparticles and their use in pyranopyrazles synthesis

    Institute of Scientific and Technical Information of China (English)

    Sneha Yadav; Jitender M. Khurana

    2015-01-01

    A novel, biochemical, and eco-friendly method has been developed for the synthesis of Ag nanopar-ticles using an aqueous leaf extract of readily accessibleCinnamomum tamala as reducing and stabi-lizing agents. These Ag nanoparticles were used to catalyze the synthesis of pyranopyrazoles. The green nature and ease of recovery and reusability of the catalyst, together with high yields of prod-ucts, make this protocol attractive and useful.

  7. Cascade synthesis of a gold nanoparticle-network polymer composite

    Science.gov (United States)

    Grubjesic, Simonida; Ringstrand, Bryan S.; Jungjohann, Katherine L.; Brombosz, Scott M.; Seifert, Sönke; Firestone, Millicent A.

    2016-01-01

    The multi-step, cascade synthesis of a self-supporting, hierarchically-structured gold nanoparticle hydrogel composite is described. The composite is spontaneously prepared from a non-covalent, lamellar lyotropic mesophase composed of amphiphiles that support the reactive constituents, a mixture of hydroxyl- and acrylate-end-derivatized PEO117-PPO47-PEO117 and [AuCl4]-. The reaction sequence begins with the auto-reduction of aqueous [AuCl4]- by PEO117-PPO47-PEO117 which leads to both the production of Au NPs and the free radical initiated polymerization and crosslinking of the acrylate end-derivatized PEO117-PPO47-PEO117 to yield a network polymer. Optical spectroscopy and TEM monitored the reduction of [AuCl4]-, formation of large aggregated Au NPs and oxidative etching into a final state of dispersed, spherical Au NPs. ATR/FT-IR spectroscopy and thermal analysis confirms acrylate crosslinking to yield the polymer network. X-ray scattering (SAXS and WAXS) monitored the evolution of the multi-lamellar structured mesophase and revealed the presence of semi-crystalline PEO confined within the water layers. The hydrogel could be reversibly swollen without loss of the well-entrained Au NPs with full recovery of composite structure. Optical spectroscopy shows a notable red shift (Δλ ~ 45 nm) in the surface plasmon resonance between swollen and contracted states, demonstrating solvent-mediated modulation of the internal NP packing arrangement.The multi-step, cascade synthesis of a self-supporting, hierarchically-structured gold nanoparticle hydrogel composite is described. The composite is spontaneously prepared from a non-covalent, lamellar lyotropic mesophase composed of amphiphiles that support the reactive constituents, a mixture of hydroxyl- and acrylate-end-derivatized PEO117-PPO47-PEO117 and [AuCl4]-. The reaction sequence begins with the auto-reduction of aqueous [AuCl4]- by PEO117-PPO47-PEO117 which leads to both the production of Au NPs and the free radical

  8. Green Synthesis of antibacterial Zinc oxide Nanoparticles using biopolymer Azadirachtaindica gum

    Directory of Open Access Journals (Sweden)

    A.Geetha

    2016-05-01

    Full Text Available The progress of green chemistry in the synthesis of nanoparticles with use of plants has engrossed a great attention nowadays due to its inexpensive, simple, non-toxic and environmental-friendly nature. The present study has been undertaken to prepare Azadirachtaindicagum stabilized ZnO nanoparticles with multifunctional properties. The prepared nanoparticles were characterized by FT-IR, XRD, FE-SEM and UV-Vis absorption studies. It was clear from XRD pattern that nanoparticles were crystallized in hexagonal wurtzite structure. The average size of the nanoparticles was found to be 30-60nm. The synthesized nanoparticles exhibited potent antibacterial activity against E. coli and S. aureus.

  9. Synthesis of photoactive AgCl/SBA-15 by conversion of silver nanoparticles into stable AgCl nanoparticles

    Science.gov (United States)

    Zienkiewicz-Strzałka, M.; Pikus, S.

    2013-01-01

    In this work the results of synthesis the ordered mesoporous silica (SBA-15) in the presence of stable silver nanoparticles were presented. It has been proven that the proposed method leads to the synthesis of SBA-15 nanocomposite containing silver chloride nanoparticles, formed by the transformation of silver nanoparticles in the acidic conditions. Proposed one-pot procedure is simple and the one requirement is to prepare a stable solution of silver nanoparticles. In this work, silver nanoparticles were obtained during chemical reduction of [Ag(NH3)2]+ ions by formaldehyde. Silver nanoparticles solution can be used as a silver chloride source due to the application of the same polymer as a stabilizer of nanocrystals and structure directing agent of SBA-15. The final AgCl/SBA-15 materials show excellent structural ordering characteristic for this type of materials confirmed by diffraction measurements in range of small angles 2θ, transmission electron microscopy (TEM) and nitrogen adsorption/desorption measurements. AgCl nanoparticles were identified by diffraction measurements as chlorargyrite phase. The presence of silver nanoparticles in initial solution and their absence after synthesis were confirmed by UV-vis measurements. The photoactivity of obtained AgCl/SBA-15 composite was tested in reaction of organic impurities photodegradation.

  10. Synthesis of Multifunctional Nanoparticles for Cancer Diagnostics and Therapeutics

    Science.gov (United States)

    Fang, Chen

    2011-12-01

    Magnetic nanoparticles (MNPs) have attracted enormous research attention due to their unique magnetic properties that enable the detection by the non-invasive medical imaging modality---magnetic resonance imaging (MRI). By incorporating advanced features, such as specific targeting, multimodality, therapeutic delivery, the detectability and applicability of MNPs have been dramatically expanded. Smart and rational design on structure, composition and surface chemistry is essential to achieving desired properties in MNP systems, such as high sensitivity and colloidal stability, target specificity and/or multimodality. The goal of this research is to develop MNP-based platforms for the detection, diagnosis and treatment of cancer. MNPs with high contrast enhancement were coated with poly(ethylene glycol) (PEG)-based polymers to render aqueous stability and confer therapeutic-loading capability. Tumor-specific MNPs were developed by functionalization of nanoparticles with chlorotoxin (CTX) or arginine-glycine-aspartic acid (RGD) that targets, respectively, MMP-2 receptor or alphavbeta3 integrin overexpressed on a variety of cancer cells. The effects of ligands' molecular targets on the temporal and spatial distribution of MNPs within tumors were also investigated both in vitro and in vivo. All MNPs exhibited excellent long-term stability in cell culture media. CTX-labeled MNP exhibited sustained accumulation, penetration and distribution in the tumor mass. These findings revealed the influence of the targeting ligands on the intratumoral distribution of the ligand-enabled nanoprobes. To demonstrate the ability of nanoparticles as drug carrier, anthracyline chemotherapeutic drugs doxorubicin and mitoxantrone were attached to iron oxide nanoparticles. The theragnostic nanoparticles showed sufficient contrast enhancement and comparable anti-neoplastic efficacy in vitro. With flexible surface chemistry, our nanoparticle platform can be used in a modular fashion to

  11. One-pot facile green synthesis of biocidal silver nanoparticles

    Science.gov (United States)

    Nudrat Hazarika, Shabiha; Gupta, Kuldeep; Shamin, Khan Naseem Ahmed Mohammed; Bhardwaj, Pushpender; Boruah, Ratan; Yadav, Kamlesh K.; Naglot, Ashok; Deb, P.; Mandal, M.; Doley, Robin; Veer, Vijay; Baruah, Indra; Namsa, Nima D.

    2016-07-01

    The plant root extract mediated green synthesis method produces monodispersed spherical shape silver nanoparticles (AgNPs) with a size range of 15-30 nm as analyzed by atomic force and transmission electron microscopy. The material showed potent antibacterial and antifungal properties. Synthesized AgNPs display a characteristic surface plasmon resonance peak at 420 nm in UV-Vis spectroscopy. X-ray diffractometer analysis revealed the crystalline and face-centered cubic geometry of in situ prepared AgNPs. Agar well diffusion and a colony forming unit assay demonstrated the potent biocidal activity of AgNPs against Staphylococcus aureus, Escherichia coli, Bacillus subtilis, Klebsiella pneumoniae, Pseudomonas diminuta and Mycobacterium smegmatis. Intriguingly, the phytosynthesized AgNPs exhibited activity against pathogenic fungi, namely Trichophyton rubrum, Aspergillus versicolor and Candida albicans. Scanning electron microscopy observations indicated morphological changes in the bacterial cells incubated with silver nanoparticles. The genomic DNA isolated from the bacteria was incubated with an increasing concentration of AgNPs and the replication fidelity of 16S rDNA was observed by performing 18 and 35 cycles PCR. The replication efficiency of small (600 bp) and large (1500 bp) DNA fragments in the presence of AgNPs were compromised in a dose-dependent manner. The results suggest that the Thalictrum foliolosum root extract mediated synthesis of AgNPs could be used as a promising antimicrobial agent against clinical pathogens.

  12. One-step green synthesis and characterization of plant protein-coated mercuric oxide (HgO) nanoparticles: antimicrobial studies

    Science.gov (United States)

    Das, Amlan Kumar; Marwal, Avinash; Sain, Divya; Pareek, Vikram

    2015-03-01

    The present study demonstrates the bioreductive green synthesis of nanosized HgO using flower extracts of an ornamental plant Callistemon viminalis. The flower extracts of Callistemon viminalis seem to be environmentally friendly, so this protocol could be used for rapid production of HgO. Till date, there is no report of synthesis of nanoparticles using flower extract of Callistemon viminalis. Mercuric acetate was taken as the metal precursor in the present experiment. The flower extract was found to act as a reducing as well as a stabilizing agent. The phytochemicals present in the flower extract act as reducing agent which include proteins, saponins, phenolic compounds, phytosterols, and flavonoids. FT-IR spectroscopy confirmed that the extract had the ability to act as a reducing agent and stabilizer for HgO nanoparticles. The formation of the plant protein-coated HgO nanoparticles was first monitored using UV-Vis absorption spectroscopy. The UV-Vis spectroscopy revealed the formation of HgO nanoparticles by exhibiting the typical surface plasmon absorption maxima at 243 nm. The average particle size formed ranges from 2 to 4 nm. The dried form of synthesized nanoparticles was further characterized using TGA, XRD, TEM, and FTIR spectroscopy. FT-IR spectra of synthesized HgO nanoparticles were performed to identify the possible bio-molecules responsible for capping and stabilization of nanoparticles, which confirm the formation of plant protein-coated HgO nanoparticles that is further corroborated by TGA study. The optical band gap of HgO nanoparticle was measured to be 2.48 eV using cutoff wavelength which indicates that HgO nanoparticles can be used in metal oxide semiconductor-based photovoltaic cells. A possible core-shell structure of the HgO nanobiocomposite has been proposed.

  13. Synthesis of lanthanum tungstate interconnecting nanoparticles by high voltage electrospinning

    Energy Technology Data Exchange (ETDEWEB)

    Keereeta, Yanee, E-mail: ynkeereeta@gmail.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thongtem, Titipun, E-mail: ttpthongtem@yahoo.com [Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thongtem, Somchai [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand)

    2015-10-01

    Graphical abstract: - Highlights: • La{sub 2}(WO{sub 4}){sub 3} as one of semiconducting materials. • H.V. electrospinning was used to synthesize La{sub 2}(WO{sub 4}){sub 3} interconnecting nanoparticles. • A promising material for photoemission. - Abstract: Lanthanum tungstate (La{sub 2}(WO{sub 4}){sub 3}) interconnecting nanoparticles in the shape of fibers were successfully synthesized by electrospinning in combination with high temperature calcination. In this research, calcination temperature for the synthesis of the fibers evidently influenced the diameter, morphology and crystalline degree. The crystalline monoclinic La{sub 2}(WO{sub 4}){sub 3} fibers with 200–700 nm in diameter, two main Raman peaks at 945 and 927 cm{sup −1}, FTIR stretching modes at 936 and 847 cm{sup −1}, 2.02 eV energy gap and 415–430 nm blue emission were synthesized by calcination of inorganic/organic hybrid fibers at 750 °C for 5 h, characterized by X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, UV–visible spectroscopy and photoluminescence (PL) spectroscopy. The surface of the composite fibers before calcination was very smooth. Upon calcination the composite fibers at 750 °C for 5 h, they were transformed into nanoparticles join together in the shape of fibers with rough surface.

  14. Synthesis, Characterization and Properties of Nanoparticles of Intermetallic Compounds

    Energy Technology Data Exchange (ETDEWEB)

    DiSalvo, Francis J. [Cornell Univ., Ithaca, NY (United States)

    2015-03-12

    The research program from 2010 to the end of the grant focused on understanding the factors important to the synthesis of single phase intermetallic nano-particles (NPs), their size, crystalline order, surface properties and electrochemical activity. The synthetic method developed is a co-reduction of mixtures of single metal precursors by strong, soluble reducing agents in a non-protic solvent, tetrahydrofuran (THF). With some exceptions, the particles obtained by room temperature reduction are random alloys that need to be annealed at modest temperatures (200 to 600 °C) in order to develop an ordered structure. To avoid significant particle size growth and agglomeration, the particles must be protected by surface coatings. We developed a novel method of coating the metal nanoparticles with KCl, a by-product of the reduction reaction if the proper reducing agents are employed. In that case, a composite product containing individual metal nanoparticles in a KCl matrix is obtained. The composite can be heated to at least 600 °C without significant agglomeration or growth in particle size. Washing the annealed product in the presence of catalyst supports in ethylene glycol removes the KCl and deposits the particles on the support. Six publications present the method and its application to producing and studying new catalyst/support combinations for fuel cell applications. Three publications concern the use of related methods to explore new lithium-sulfur battery concepts.

  15. Facile and green synthesis of silver nanoparticles using oxidized pectin

    Energy Technology Data Exchange (ETDEWEB)

    Tummalapalli, Mythili; Deopura, B.L. [Bioengineering Lab, Department of Textile Technology, Indian Institute of Technology, Hauz Khas, New Delhi 110016 (India); Alam, M.S. [Department of Chemistry, Jamia Hamdard, New Delhi 110062 (India); Gupta, Bhuvanesh, E-mail: bgupta@textile.iitd.ernet.in [Bioengineering Lab, Department of Textile Technology, Indian Institute of Technology, Hauz Khas, New Delhi 110016 (India)

    2015-05-01

    In the current work, an alternative route for facile synthesis of nanosilver is reported. Oxidized pectin has been used as the reducing agent as well as the stabilizing agent, resulting in the formation of oxidized pectin-nanosilver (OP-NS) core sheath nanohydrogels. The effect of reaction parameters on the synthesized nanoparticles is investigated. The structural and morphological features have been analyzed using X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM) respectively. The crystal size of the synthesized nanosilver was calculated to be 28.76 nm. While the average size of the core sheath structure varied from 289 nm to 540 nm, the size of the silver nanoparticle entities at the core varied from 100 nm to 180 nm, with variation in reaction time. From the morphological examination, it could be seen that flower like nanostructures are formed with nanosilver in the core surrounded by a polymeric halo. - Highlights: • In-situ reduction of silver nitrate to nanosilver was carried out using oxidized pectin. • Oxidized pectin-nanosilver nanohydrogels were synthesized. • Nanoparticles with flower like morphology and face centered cubic crystal structure were fabricated.

  16. Electrochemical synthesis, characterisation and phytogenic properties of silver nanoparticles

    Science.gov (United States)

    Singaravelan, R.; Bangaru Sudarsan Alwar, S.

    2015-11-01

    This work exemplifies a simple and rapid method for the synthesis of silver nanodendrite with a novel electrochemical technique. The antibacterial activity of these silver nanoparticles (Ag NPs) against pathogenic bacteria was investigated along with the routine study of optical and spectral characterisation. The optical properties of the silver nanoparticles were characterised by diffuse reflectance spectroscopy. The optical band gap energy of the electrodeposited Ag NPs was determined from the diffuse reflectance using Kubelka-Munk formula. X-ray diffraction (XRD) studies were carried out to determine the crystalline nature of the silver nanoparticles which confirmed the formation of silver nanocrystals. The XRD pattern revealed that the electrodeposited Ag NPs were in the cubic geometry with dendrite preponderance. The average particle size and the peak broadening were deliberated using Debye-Scherrer equation and lattice strain due to the peak broadening was studied using Williamson-Hall method. Surface morphology of the Ag NPs was characterised by high-resolution scanning electron microscope and the results showed the high degree of aggregation in the particles. The antibacterial activity of the Ag NPs was evaluated and showed unprecedented level antibacterial activity against multidrug resistant strains such as Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumonia and Escherichia coli in combination with Streptomycin.

  17. Prodigious Effects of Concentration Intensification on Nanoparticle Synthesis: A High-Quality, Scalable Approach

    KAUST Repository

    Williamson, Curtis B.

    2015-12-23

    © 2015 American Chemical Society. Realizing the promise of nanoparticle-based technologies demands more efficient, robust synthesis methods (i.e., process intensification) that consistently produce large quantities of high-quality nanoparticles (NPs). We explored NP synthesis via the heat-up method in a regime of previously unexplored high concentrations near the solubility limit of the precursors. We discovered that in this highly concentrated and viscous regime the NP synthesis parameters are less sensitive to experimental variability and thereby provide a robust, scalable, and size-focusing NP synthesis. Specifically, we synthesize high-quality metal sulfide NPs (<7% relative standard deviation for Cu2-xS and CdS), and demonstrate a 10-1000-fold increase in Cu2-xS NP production (>200 g) relative to the current field of large-scale (0.1-5 g yields) and laboratory-scale (<0.1 g) efforts. Compared to conventional synthesis methods (hot injection with dilute precursor concentration) characterized by rapid growth and low yield, our highly concentrated NP system supplies remarkably controlled growth rates and a 10-fold increase in NP volumetric production capacity (86 g/L). The controlled growth, high yield, and robust nature of highly concentrated solutions can facilitate large-scale nanomanufacturing of NPs by relaxing the synthesis requirements to achieve monodisperse products. Mechanistically, our investigation of the thermal and rheological properties and growth rates reveals that this high concentration regime has reduced mass diffusion (a 5-fold increase in solution viscosity), is stable to thermal perturbations (64% increase in heat capacity), and is resistant to Ostwald ripening.

  18. Gas-Phase Combustion Synthesis of Nonoxide Nanoparticles in Microgravity

    Science.gov (United States)

    Axelbaum, R. L.; Kumfer, B. M.; Sun, Z.; Chao, B. H.

    2001-01-01

    Gas-phase combustion synthesis is a promising process for creating nanoparticles for the growing nanostructure materials industry. The challenges that must be addressed are controlling particle size, preventing hard agglomerates, maintaining purity, and, if nonoxides are synthesized, protecting the particles from oxidation and/or hydrolysis during post-processing. Sodium-halide Flame Encapsulation (SFE) is a unique methodology for producing nonoxide nanoparticles that addresses these challenges. This flame synthesis process incorporates sodium and metal-halide chemistry, resulting in nanoparticles that are encapsulated in salt during the early stages of their growth in the flame. Salt encapsulation has been shown to allow control of particle size and morphology, while serving as an effective protective coating for preserving the purity of the core particles. Metals and compounds that have been produced using this technology include Al, W, Ti, TiB2, AlN, and composites of W-Ti and Al-AlN. Oxygen content in SFE synthesized nano- AlN has been measured by neutron activation analysis to be as low as 0.54wt.%, as compared to over 5wt.% for unprotected AlN of comparable size. The overall objective of this work is to study the SFE process and nano-encapsulation so that they can be used to produce novel and superior materials. SFE experiments in microgravity allow the study of flame and particle dynamics without the influence of buoyancy forces. Spherical sodium-halide flames are produced in microgravity by ejecting the halide from a spherical porous burner into a quiescent atmosphere of sodium vapor and argon. Experiments are performed in the 2.2 sec Drop Tower at the NASA-Glenn Research Center. Numerical models of the flame and particle dynamics were developed and are compared with the experimental results.

  19. Weissella oryzae DC6-facilitated green synthesis of silver nanoparticles and their antimicrobial potential.

    Science.gov (United States)

    Singh, Priyanka; Kim, Yeon J; Wang, Chao; Mathiyalagan, Ramya; Yang, Deok C

    2016-09-01

    Nanoparticles and nanomaterials are at the prominent edge of the rapidly developing field of nanotechnology. Recently, nanoparticle synthesis using biological resources has been found to be a new area with considerable prospects for development. Biological systems are the masters of ambient condition chemistry and are able to synthesize nanoparticles by utilizing metal salts. In the perspective of the current initiative to develop green technologies for the synthesis of nanoparticles, microorganisms are of considerable interest. Thus, the present study describes a bacterial strain-Weissella oryzae DC6-isolated from mountain ginseng, for the green and facile synthesis of silver nanoparticles. The particles were synthesized effectively without the need for any supplementary modification to maintain stability. The synthesized nanoparticles were evaluated by several instrumental techniques, comprising ultraviolet-visible spectrophotometry, field emission transmission electron microscopy, energy dispersive X-ray spectroscopy, elemental mapping, X-ray diffraction, and dynamic light scattering. In addition, the biosynthesized silver nanoparticles were explored for their antimicrobial activity against clinical pathogens including Vibrio parahaemolyticus, Bacillus cereus, Bacillus anthracis, Staphylococcus aureus, Escherichia coli, and Candida albicans. Furthermore, the potential of nanoparticles has been observed for biofilm inhibition against Staphylococcus aureus and Pseudomonas aeruginosa. Thus, the synthesis of silver nanoparticles by the strain W. oryzae DC6 may serve as a simple, green, cost-effective, consistent, and harmless method to produce antimicrobial silver nanoparticles. PMID:26212222

  20. Impact and mechanism of TiO2 nanoparticles on DNA synthesis in vitro

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The impact of TiO2 nanoparticles on DNA synthesis in vitro in the dark and the molecular mechanism of such impact were studied. The impact of TiO2 nanoparticles on DNA synthesis was investigated by adding TiO2 nanoparticles in different sizes and at various concentrations into the polymerase chain reaction (PCR) system. TiO2 nanoparticles were premixed with the DNA polymerase, the primer or the template, respectively and then the supernatant and the precipitation of each mixture were added into the PCR system separately to observe the impact on DNA synthesis. Sequentially the interaction be- tween TiO2 nanoparticles and the DNA polymerase, the primer or the template was further analyzed by using UV-visible spectroscopy and polyacrylamide gel electrophoresis (PAGE). The results suggest that TiO2 nanoparticles inhibit DNA synthesis in the PCR system in the dark more severely than mi- croscale TiO2 particles at the equivalent concentration and the inhibition effect of TiO2 nanoparticles is concentration dependent. The molecular mechanism of such inhibition is that in the dark, TiO2 nanoparticles interact with the DNA polymerase through physical adsorption while TiO2 nanoparticles do with the primer or the template in a chemical adsorption manner. The disfunction levels of the bio-molecules under the impact of TiO2 nanoparticles are in the following order: the primer > the tem- plate > the DNA polymerase.

  1. T1-MRI Fluorescent Iron Oxide Nanoparticles by Microwave Assisted Synthesis

    Directory of Open Access Journals (Sweden)

    Riju Bhavesh

    2015-11-01

    Full Text Available Iron oxide nanoparticles have long been studied as a T2 contrast agent in MRI due to their superparamagnetic behavior. T1-based positive contrast, being much more favorable for clinical application due to brighter and more accurate signaling is, however, still limited to gadolinium- or manganese-based imaging tools. Though being the only available commercial positive-contrast agents, they lack an efficient argument when it comes to biological toxicity and their circulatory half-life in blood. The need arises to design a biocompatible contrast agent with a scope for easy surface functionalization for long circulation in blood and/or targeted imaging. We hereby propose an extremely fast microwave synthesis for fluorescein-labeled extremely-small iron oxide nanoparticles (fdIONP, in a single step, as a viable tool for cell labeling and T1-MRI. We demonstrate the capabilities of such an approach through high-quality magnetic resonance angiographic images of mice.

  2. Aqueous based reflux method for green synthesis of nanostructures: Application in CZTS synthesis.

    Science.gov (United States)

    Aditha, Sai Kiran; Kurdekar, Aditya Dileep; Chunduri, L A Avinash; Patnaik, Sandeep; Kamisetti, Venkataramaniah

    2016-01-01

    The aqueous based reflux method useful for the green synthesis of nanostructures is described in detail. In this method, the parameters: the order of addition of precursors, the time of the reflux and the cooling rate should be optimized in order to obtain the desired phase and morphology of the nanostructures. The application of this method is discussed with reference to the synthesis of CZTS nanoparticles which have great potential as an absorber material in the photovoltaic devices. The highlights of this method are:•Simple.•Low cost.•Aqueous based. PMID:27408826

  3. Chemoelectronic circuits based on metal nanoparticles.

    Science.gov (United States)

    Yan, Yong; Warren, Scott C; Fuller, Patrick; Grzybowski, Bartosz A

    2016-07-01

    To develop electronic devices with novel functionalities and applications, various non-silicon-based materials are currently being explored. Nanoparticles have unique characteristics due to their small size, which can impart functions that are distinct from those of their bulk counterparts. The use of semiconductor nanoparticles has already led to improvements in the efficiency of solar cells, the processability of transistors and the sensitivity of photodetectors, and the optical and catalytic properties of metal nanoparticles have led to similar advances in plasmonics and energy conversion. However, metals screen electric fields and this has, so far, prevented their use in the design of all-metal nanoparticle circuitry. Here, we show that simple electronic circuits can be made exclusively from metal nanoparticles functionalized with charged organic ligands. In these materials, electronic currents are controlled by the ionic gradients of mobile counterions surrounding the 'jammed' nanoparticles. The nanoparticle-based electronic elements of the circuitry can be interfaced with metal nanoparticles capable of sensing various environmental changes (humidity, gas, the presence of various cations), creating electronic devices in which metal nanoparticles sense, process and ultimately report chemical signals. Because the constituent nanoparticles combine electronic and chemical sensing functions, we term these systems 'chemoelectronic'. The circuits have switching times comparable to those of polymer electronics, selectively transduce parts-per-trillion chemical changes into electrical signals, perform logic operations, consume little power (on the scale of microwatts), and are mechanically flexible. They are also 'green', in the sense that they comprise non-toxic nanoparticles cast at room temperature from alcohol solutions. PMID:26974958

  4. Chemoelectronic circuits based on metal nanoparticles

    Science.gov (United States)

    Yan, Yong; Warren, Scott C.; Fuller, Patrick; Grzybowski, Bartosz A.

    2016-07-01

    To develop electronic devices with novel functionalities and applications, various non-silicon-based materials are currently being explored. Nanoparticles have unique characteristics due to their small size, which can impart functions that are distinct from those of their bulk counterparts. The use of semiconductor nanoparticles has already led to improvements in the efficiency of solar cells, the processability of transistors and the sensitivity of photodetectors, and the optical and catalytic properties of metal nanoparticles have led to similar advances in plasmonics and energy conversion. However, metals screen electric fields and this has, so far, prevented their use in the design of all-metal nanoparticle circuitry. Here, we show that simple electronic circuits can be made exclusively from metal nanoparticles functionalized with charged organic ligands. In these materials, electronic currents are controlled by the ionic gradients of mobile counterions surrounding the ‘jammed’ nanoparticles. The nanoparticle-based electronic elements of the circuitry can be interfaced with metal nanoparticles capable of sensing various environmental changes (humidity, gas, the presence of various cations), creating electronic devices in which metal nanoparticles sense, process and ultimately report chemical signals. Because the constituent nanoparticles combine electronic and chemical sensing functions, we term these systems ‘chemoelectronic’. The circuits have switching times comparable to those of polymer electronics, selectively transduce parts-per-trillion chemical changes into electrical signals, perform logic operations, consume little power (on the scale of microwatts), and are mechanically flexible. They are also ‘green’, in the sense that they comprise non-toxic nanoparticles cast at room temperature from alcohol solutions.

  5. Conductivity dependence on synthesis parameters in hydrothermally synthesized ceria nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Anis-ur-Rehman, M., E-mail: marehman@comsats.edu.pk; Saleemi, A.S.; Abdullah, A.

    2013-12-05

    Highlights: •Facile synthesis of CeO{sub 2} with composite mediated hydrothermal method is done. •Synthesis parameters significantly effect on conduction. •Enhanced dc electrical conductivity (0.3386 S cm{sup −1}) is observed at 700 °C. •Better ac conductivity is observed 2.661 S cm{sup −1} at 700 °C for 3 MHz. •Potential material for electrolyte in fuel cells for higher efficiencies. -- Abstract: Nanoparticles of cerium oxide were synthesized by Composite Mediated Hydrothermal Approach (CMHA). The synthesis conditions were optimized to enhance the conduction properties and for narrow range of nanocrystallites. The synthesis parameters like hydrothermal treatment temperature (at 180 °C and 220 °C) and time (for 45 min, 70 min and 90 min) were optimized. The structural properties of the prepared ceria were examined by X-ray diffraction (XRD) data. Scherrer’s formula was used to calculate the crystallite sizes of average and most intense peak. Temperature dependent dc conductivity was measured in temperature range 200–700 °C and found to be increasing with the increase in measuring temperature and controlling the other synthesis conditions. The frequency dependent ac conductivity and dielectric properties were measured in frequency range 20 Hz–3 MHz at different temperatures. The ac conductivity increased (from 0.00091 to 2.661 S cm{sup −1}) with the increase in temperature (from 200 to 700 °C). Raman spectrum was observed for the different bands of cerium oxide and oxygen vacancies at 514 nm excitation laser line.

  6. Synthesis of fluorescent metal nanoparticles in aqueous solution by photochemical reduction

    KAUST Repository

    Kshirsagar, Prakash

    2014-01-06

    A facile green chemistry approach for the synthesis of sub-5 nm silver and gold nanoparticles is reported. The synthesis was achieved by a photochemical method using tyrosine as the photoreducing agent. The size of the gold and silver nanoparticles was about 3 and 4 nm, respectively. The nanoparticles were characterized using x-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy and photoluminescence spectroscopy. Both silver and gold nanoparticles synthesized by this method exhibited fluorescence properties and their use for cell imaging applications has been demonstrated. © 2014 IOP Publishing Ltd.

  7. Molten-droplet synthesis of composite CdSe hollow nanoparticles

    KAUST Repository

    Gullapalli, Sravani

    2012-11-16

    Many colloidal synthesis routes are not scalable to high production rates, especially for nanoparticles of complex shape or composition, due to precursor expense and hazards, low yields, and the large number of processing steps. The present work describes a strategy to synthesize hollow nanoparticles (HNPs) out of metal chalcogenides, based on the slow heating of a low-melting-point metal salt, an elemental chalcogen, and an alkylammonium surfactant in octadecene solvent. The synthesis and characterization of CdSe HNPs with an outer diameter of 15.6 ± 3.5 nm and a shell thickness of 5.4 ± 0.9 nm are specifically detailed here. The HNP synthesis is proposed to proceed with the formation of alkylammonium-stabilized nano-sized droplets of molten cadmium salt, which then come into contact with dissolved selenium species to form a CdSe shell at the droplet surface. In a reaction-diffusion mechanism similar to the nanoscale Kirkendall effect it is speculated that the cadmium migrates outwardly through this shell to react with more selenium, causing the CdSe shell to thicken. The proposed CdSe HNP structure comprises a polycrystalline CdSe shell coated with a thin layer of amorphous selenium. Photovoltaic device characterization indicates that HNPs have improved electron transport characteristics compared to standard CdSe quantum dots, possibly due to this selenium layer. The HNPs are colloidally stable in organic solvents even though carboxylate, phosphine, and amine ligands are absent; stability is attributed to octadecene-selenide species bound to the particle surface. This scalable synthesis method presents opportunities to generate hollow nanoparticles with increased structural and compositional variety. © 2012 IOP Publishing Ltd.

  8. Recent advances in the synthesis of Fe3O4@AU core/shell nanoparticles

    Science.gov (United States)

    Salihov, Sergei V.; Ivanenkov, Yan A.; Krechetov, Sergei P.; Veselov, Mark S.; Sviridenkova, Natalia V.; Savchenko, Alexander G.; Klyachko, Natalya L.; Golovin, Yury I.; Chufarova, Nina V.; Beloglazkina, Elena K.; Majouga, Alexander G.

    2015-11-01

    Fe3O4@Au core/shell nanoparticles have unique magnetic and optical properties. These nanoparticles are used for biomedical applications, such as magnetic resonance imaging, photothermal therapy, controlled drug delivery, protein separation, biosensors, DNA detection, and immunosensors. In this review, recent methods for the synthesis of core/shell nanoparticles are discussed. We divided all of the synthetic methods in two groups: methods of synthesis of bi-layer structures and methods of synthesis of multilayer composite structures. The latter methods have a layer of "glue" material between the core and the shell.

  9. A modified method for barium titanate nanoparticles synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Ashiri, R., E-mail: ro_ashiri@iaud.ac.ir [Department of Materials Science and Engineering, Dezful Branch, Islamic Azad University, P.O. Box 313, Dezful (Iran, Islamic Republic of); Nemati, Ali [Department of Materials Science and Engineering, Sharif University of Technology, P.O. Box 11365-9466, Tehran (Iran, Islamic Republic of); Sasani Ghamsari, M. [Solid State Lasers Research Group, Laser and Optics Research School, NSTRI, P.O. Box 11365-8486, Tehran (Iran, Islamic Republic of); Sanjabi, S. [Nanomaterials Group, Department of Materials Engineering, Tarbiat Modares University, P.O. Box 14115-143, Tehran (Iran, Islamic Republic of); Aalipour, M. [Department of Materials Science and Engineering, Sharif University of Technology, P.O. Box 11365-9466, Tehran (Iran, Islamic Republic of)

    2011-12-15

    Graphical abstract: TEM micrograph of BaTiO{sub 3} powders synthesized at 800 Degree-Sign C for 1 h and SAED pattern (inset) of BaTiO{sub 3} powders. In this research, a modified, cost efficient and quick sol-gel procedure was used for preparation of BaTiO{sub 3} nanoparticles. Highlights: Black-Right-Pointing-Pointer A modified process was used for preparation. Black-Right-Pointing-Pointer The modified process led to preparation of finer BaTiO{sub 3} nanoparticles in shorter period of time and lower temperature contrary to previous researches. Black-Right-Pointing-Pointer The proposed procedure seems to be more preferable for mass production. -- Abstract: In this research, a modified, cost effective sol-gel procedure applied to synthesize BaTiO{sub 3} nanoparticles. XRD and electron microscopy (SEM and TEM) applied for microstructural characterization of powders. The obtained results showed that the type of precursors, their ratio and the hydrolysis conditions had a great effect on time, temperature and therefore the costs of the synthesis process. By selection, utilization of optimized precursor's type, hydrolysis conditions, fine cubic BaTiO{sub 3} nanoparticles were synthesized at low temperature and in short time span (1 h calcination at 800 Degree-Sign C). The proposed procedure seems to be more preferable for mass production. The result indicated that the polymorphic transformation to tetragonal (ferroelectric characteristic) occurred at 900 Degree-Sign C, which might be an indication of being nanosized.

  10. SYNTHESIS OF NiO NANOPARTICLES IN ETHYLENE GLYCOL

    Institute of Scientific and Technical Information of China (English)

    Desheng Ai; Xiaming Dai; Qingfeng Li; Changsheng Deng; Shinhoo Kang

    2004-01-01

    NiO nanoparticles with well-dispersed property were prepared via a wet chemical method in ethylene glycol (EG) without soluble polymer as a protective agent. The mechanism of chemical process was proposed based on color change during the experiment. The dispersion function of EG was discussed.

  11. Hydrothermal Synthesis and Processing of Barium Titanate Nanoparticles Embedded in Polymer Films.

    Science.gov (United States)

    Toomey, Michael D; Gao, Kai; Mendis, Gamini P; Slamovich, Elliott B; Howarter, John A

    2015-12-30

    Barium titanate nanoparticles embedded in flexible polymer films were synthesized using hydrothermal processing methods. The resulting films were characterized with respect to material composition, size distribution of nanoparticles, and spatial location of particles within the polymer film. Synthesis conditions were varied based on the mechanical properties of the polymer films, ratio of polymer to barium titanate precursors, and length of aging time between initial formulations of the solution to final processing of nanoparticles. Block copolymers of poly(styrene-co-maleic anhydride) (SMAh) were used to spatially separate titanium precursors based on specific chemical interactions with the maleic anhydride moiety. However, the glassy nature of this copolymer restricted mobility of the titanium precursors during hydrothermal processing. The addition of rubbery butadiene moieties, through mixing of the SMAh with poly(styrene-butadiene-styrene) (SBS) copolymer, increased the nanoparticle dispersion as a result of greater diffusivity of the titanium precursor via higher mobility of the polymer matrix. Additionally, an aminosilane was used as a means to retard cross-linking in polymer-metalorganic solutions, as the titanium precursor molecules were shown to react and form networks prior to hydrothermal processing. By adding small amounts of competing aminosilane, excessive cross-linking was prevented without significantly impacting the quality and composition of the final barium titanate nanoparticles. X-ray diffraction and X-ray photoelectron spectroscopy were used to verify nanoparticle compositions. Particle sizes within the polymer films were measured to be 108 ± 5 nm, 100 ± 6 nm, and 60 ± 5 nm under different synthetic conditions using electron microscopy. Flexibility of the films was assessed through measurement of the glass transition temperature using dynamic mechanical analysis. Dielectric permittivity was measured using an impedance analyzer. PMID

  12. Interfacial synthesis and functionality of self-stabilized polydiaminonaphthalene nanoparticles.

    Science.gov (United States)

    Li, Xin-Gui; Zhang, Jia-Li; Huang, Mei-Rong

    2012-08-01

    A simple and effective template-free synthesis method for nanosized conducting polymers with self-stability and functionality is a main challenge. Herein, a strategy is reported for the facile synthesis of poly(1,5-diaminonaphthalene) nanospherical particles by an interfacial miniemulsion oxidative polymerization of 1,5-diaminonaphthalene at mobile microinterfaces between a stirred biphase without external emulsifiers. The size of the nanospheres was carefully optimized by controlling the polymerization conditions. Formation and self-stabilization mechanisms of the nanoparticles are proposed. The constantly movable and refreshed microinterface is a key to successful synthesis of the nanospheres, for significantly suppressing secondary growth leading to agglomerated particles because vigorous stirring makes as-formed self-stabilized nanospheres instantly leave the microinterfaces. The resulting nanospheres possess several advantages: clean surface, self-stability, redispersibility, semiconductivity, electroactivity, and fluorescence emission. The fluorescence emission can be quenched by specific quenchers, thus enabling low-cost, high-performance chemosensors to be obtained for the sensitive detection of Zn(II) ions in a wide linear concentration range of more than five orders of magnitude with a superior detection limit down to 1 nM.

  13. Synthesis of silver nanoparticles using leaves of Catharanthus roseus Linn. G. Don and their antiplasmodial activities

    Institute of Scientific and Technical Information of China (English)

    Ponarulselvam S; Panneerselvam C; Murugan K; Aarthi N; Kalimuthu K; Thangamani S

    2012-01-01

    Objective: To develop a novel approach for the green synthesis of silver nanoparticles using aqueous leaves extracts of Catharanthus roseus (C. roseus) Linn. G. Don which has been proven active against malaria parasite Plasmodium falciparum (P. falciparum). Methods:Characterizations were determined by using ultraviolet-visible (UV-Vis) spectrophotometry, scanning electron microscopy (SEM), energy dispersive X-ray and X-ray diffraction. Results:SEM showed the formation of silver nanoparticles with an average size of 35-55 nm. X-ray diffraction analysis showed that the particles were crystalline in nature with face centred cubic structure of the bulk silver with the broad peaks at 32.4, 46.4 and 28.0. Conclusions: It can be concluded that the leaves of C. roseus can be good source for synthesis of silver nanoparticle which shows antiplasmodial activity against P. falciparum. The important outcome of the study will be the development of value added products from medicinal plants C. roseus for biomedical and nanotechnology based industries.

  14. Synthesis of silver nanoparticles using leaves of Catharanthus roseus Linn. G. Don and their antiplasmodial activities

    Science.gov (United States)

    Ponarulselvam, S; Panneerselvam, C; Murugan, K; Aarthi, N; Kalimuthu, K; Thangamani, S

    2012-01-01

    Objective To develop a novel approach for the green synthesis of silver nanoparticles using aqueous leaves extracts of Catharanthus roseus (C. roseus) Linn. G. Don which has been proven active against malaria parasite Plasmodium falciparum (P. falciparum). Methods Characterizations were determined by using ultraviolet-visible (UV-Vis) spectrophotometry, scanning electron microscopy (SEM), energy dispersive X-ray and X-ray diffraction. Results SEM showed the formation of silver nanoparticles with an average size of 35–55 nm. X-ray diffraction analysis showed that the particles were crystalline in nature with face centred cubic structure of the bulk silver with the broad peaks at 32.4, 46.4 and 28.0. Conclusions It can be concluded that the leaves of C. roseus can be good source for synthesis of silver nanoparticle which shows antiplasmodial activity against P. falciparum. The important outcome of the study will be the development of value added products from medicinal plants C. roseus for biomedical and nanotechnology based industries. PMID:23569974

  15. Synthesis and characterization of water-dispersible core/shell Mn-doped magnetite/Au nanoparticles for proton radiotherapy

    Energy Technology Data Exchange (ETDEWEB)

    Park, Jeong Chan [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-05-15

    The surface modification of the nanomaterials is required for the biomedical use to give physiological stability, surface reactivity and targeting properties. Among many approaches for the surface modification with materials, such as polymers, organic ligands and metals, one of the most attractive ways is to employ metals. The fabrication of metal-based, monolayer coated magnetic nanoparticles has been intensively studied. However, the synthesis of metal-capped magnetic nanoparticles with monodispersities and controllable sizes is still challenged. Recently, gold-capped magnetic nanoparticles have been reported to increase stability and to provide biocompatibility. Gold-coated magnetic nanoparticles are an attractive system, which can be stabilized in biological conditions and readily functionalized through well-established surface modification chemistry. In addition, the Au coating offers plasmonic properties to magnetic nanoparticles. This makes the magnetic/Au core/shell combinations interesting for magnetic and optical applications. The monodisperse Mn:Fe3O4/Au nanoparticles have been prepared in organic solvent first and then transferred from an organic phase to an aqueous solution. The resulting core/shell-structured nanoparticles may be an attractive system for biomedical applications, which are needed both magnetic resonance imaging and optical imaging. In addition, the resulting nanoparticles may be useful for proton radiotherapy due to the enhanced therapeutic effects of secondary radiation stemmed from gold and proton beam bombardment.

  16. A High Yield Synthesis of Chalcopyrite CuInS2 Nanoparticles with Exceptional Size Control

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Chivin; Gardner, Joseph S.; Shurdha, Endrit; Margulieux, Kelsey R.; Westover, Richard D.; Lau, Lisa D.; Long, Gary; Bajracharya, Cyril; Wang, Chong M.; Thurber, Aaron P.; Punnoose, Alex; Rodriguez, Rene G.; Pak, Joshua J.

    2009-12-29

    Various I-III-VI2 semiconductor materials have been identified as promising photovoltaic materials [1, 2]. Recently, quantum dot (QD) based solar cells have attracted much attention due to their potential to replace thin film devices [3-5]. One of the major advantages of employing QDs is by simply changing the particle size they can be tuned to absorb specific wavelengths ranging from visible to infrared wavelengths [6]. Furthermore, with careful design of photovoltaic (PV) devices incorporating various sizes of nanoparticles in multiple layers, one may achieve increased solar energy absorption in one device [7, 8]. In order to facilitate QD based multilayer devices, synthetic strategies that can deliver QDs in high yields with precise size control are essential. One of the strategies to prepare QDs is to prepare nanoparticles from molecular single source precursors (SSPs), which contain all necessary elements in a single molecule. In recent years, there have been several reports on the formation of CuInS2 nanoparticles through the decomposition of SSPs using thermolysis [9-14], photolysis [18], and microwave irradiation [16]. However, many of these procedures require a combination of long reaction times (10 to 24 hours) and high reaction temperatures (often exceeding 200 °C) with very little information regarding overall yields. Microwave-assisted growth of nanoparticles is generally favorable over traditional thermolysis as microwave irradiation overcomes local intermediaries and increases the microscopic temperature of the reaction [17] thus exhibiting greater homogeneity in the overall reaction temperature. This allows for nanoparticles with diameters of a few nanometers can be prepared [18], dramatic decreases in reaction times, improved product purities, all forms of precursors can be used, and reactions exhibit high reproducibility and yields [19]. For CuInS2 QDs, the Wannier-Mott bulk exciton radius is approximately 8 nm with a bandgap of 1.45 eV and QDs

  17. Synthesis in plants and plant extracts of silver nanoparticles with potent antimicrobial properties: current status and future prospects.

    Science.gov (United States)

    Mashwani, Zia-ur-Rehman; Khan, Tariq; Khan, Mubarak Ali; Nadhman, Akhtar

    2015-12-01

    Synthesis of silver nanoparticles by plants and plant extracts (green synthesis) has been developed into an important innovative biotechnology, especially in the application of such particles in the control of pathogenic bacteria. This is a safer technology, biologically and environmentally, than synthesis of silver nanoparticles by chemical or physical methods. Plants are preferable to microbes as agents for the synthesis of silver nanoparticles because plants do not need to be maintained in cell culture. The antibacterial activity of bionanoparticles has been extensively explored during the past decade. This review examines studies published in the last decade that deal with the synthesis of silver nanoparticles in plants and their antibacterial activity.

  18. Radiochemical synthesis of {sup 105g}Ag-labelled silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ichedef, C., E-mail: cigdem_ch@yahoo.com; Simonelli, F.; Holzwarth, U. [Institute for Health and Consumer Protection, European Commission, Joint Research Centre (Italy); Bagaria, J. Piella; Puntes, V. F. [Institut Català de Nanotecnologia (ICN2) (Spain); Cotogno, G.; Gilliland, D.; Gibson, N. [Institute for Health and Consumer Protection, European Commission, Joint Research Centre (Italy)

    2013-11-15

    A method for synthesis of radiolabelled silver nanoparticles is reported. The method is based on proton activation of silver metal powder, enriched in {sup 107}Ag, with a 30.7 MeV proton beam. At this proton energy {sup 105g}Ag is efficiently created, mainly via the {sup 107}Ag(p,3n){sup 105}Cd → {sup 105g}Ag reaction. {sup 105g}Ag has a half-life of 41.29 days and emits easily detectable gamma radiation on decay to {sup 105}Pd. This makes it very useful as a tracing radionuclide for experiments over several weeks or months. Following activation and a period to allow short-lived radionuclides to decay, the powder was dissolved in concentrated nitric acid in order to form silver nitrate (AgNO{sub 3}), which was used to synthesise radiolabelled silver nanoparticles via the process of sodium borohydride reduction. For comparison, non-radioactive silver nanoparticles were synthesised using commercially supplied AgNO{sub 3} in order to check if the use of irradiated Ag powder as a starting material would alter in any way the final nanoparticle characteristics. Both nanoparticle types were characterised using dynamic light scattering, zeta-potential and X-ray diffraction measurements, while additionally the non-radioactive samples were analysed by transmission electron microscopy and UV–Vis spectrometry. A hydrodynamic diameter of about 16 nm was determined for both radiolabelled and non-radioactive nanoparticles, while the electron microscopy on the non-radioactive samples indicated that the physical size of the metal NPs was (7.3 ± 1.4) nm.

  19. Synthesis and Characteristics of FePt Nanoparticle Films Under In Situ-Applied Magnetic Field.

    Science.gov (United States)

    Qian, Xu; Gao, Mo-Yun; Li, Ai-Dong; Zhou, Xiao-Yu; Liu, Xiao-Jie; Cao, Yan-Qiang; Li, Chen; Wu, Di

    2016-12-01

    In situ external magnetic field was applied during the synthesis of FePt nanoparticles via a chemical solution method. FePt nanoparticle films were prepared on Si by a drop-coating method with and without a magnetic field. Annealing at 700 °C in reductive atmosphere was explored to obtain ferromagnetic FePt L10 phase. The effect of in situ-applied magnetic field on the structure, morphology, and magnetic properties of FePt nanoparticle films was characterized. It is found that the applied magnetic field during the chemical synthesis of FePt nanoparticles plays a key role in the crystallinity and magnetic property of FePt nanoparticle films. As-synthesized FePt nanoparticles under the magnetic field are monodispersed and can be self-assembled over a larger area by a dropping method. The applied magnetic field during the synthesis of FePt nanoparticles not only significantly improves the nanoparticles' c-axis preferred orientation but also benefits the phase transition of FePt nanoparticles from face-centered cubic to face-centered tetragonal structure during the annealing process. The FePt nanoparticle films derived under magnetic field also show some magnetic anisotropy. PMID:27401088

  20. Plasma synthesis of single crystal silicon nanoparticles for novel electronic device applications

    CERN Document Server

    Bapat, A; Perrey, C R; Carter, C B; Campbell, S A; Kortshagen, U; Bapat, Ameya; Anderson, Curtis; Perrey, Christopher R.; Campbell, Stephen A.; Kortshagen, Uwe

    2004-01-01

    Single-crystal nanoparticles of silicon, several tens of nm in diameter, may be suitable as building blocks for single-nanoparticle electronic devices. Previous studies of nanoparticles produced in low-pressure plasmas have demonstrated the synthesis nanocrystals of 2-10 nm diameter but larger particles were amorphous or polycrystalline. This work reports the use of a constricted, filamentary capacitively coupled low-pressure plasma to produce single-crystal silicon nanoparticles with diameters between 20-80 nm. Particles are highly oriented with predominant cubic shape. The particle size distribution is rather monodisperse. Electron microscopy studies confirm that the nanoparticles are highly oriented diamond-cubic silicon.

  1. Room-temperature sol–gel synthesis of organic ligand-capped ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zobel, Mirijam, E-mail: mirijam.zobel@fau.de; Chatterjee, Haimantee [Friedrich-Alexander University Erlangen-Nürnberg (FAU), Department of Physics, Lehrstuhl für Kristallographie und Strukturphysik (Germany); Matveeva, Galina; Kolb, Ute [Johannes Gutenberg-Universität, Institut für Physikalische Chemie (Germany); Neder, Reinhard B., E-mail: reinhard.neder@fau.de [Friedrich-Alexander University Erlangen-Nürnberg (FAU), Department of Physics, Lehrstuhl für Kristallographie und Strukturphysik (Germany)

    2015-05-15

    Powders of zinc oxide nanoparticles with individual particle sizes below 10 nm in diameter are readily produced in base-induced sol–gel processes from ethanolic solutions of zinc acetate dihydrate. These particles are covered with acetate molecules and without further stabilization, they grow when stored as a powder. Here, we present three organic ligands, which reproducibly stabilize individual particle sizes <5 nm within the agglomerated powders for extended periods of time, up to months. Citric acid and 1,5-diphenyl-1,3,5-pentanetrione result in average diameters of 3 nm, whereas dimethyl-L-tartrate stabilizes 2.1 nm. X-ray diffraction and pair distribution function analysis were used to investigate the structural properties of the particles. TEM data confirm the individual particle size and crystallinity and show that the particles are agglomerated without structural coherence. Besides the introduction of these novel ligands for ZnO nanoparticles, we investigated, in particular, the influence of each synthesis step onto the final nanoparticle size in the powder. Previous studies often reported the employed synthesis parameters, but did not motivate the reasoning for their choice based on detailed experimental observations. Herein, we regard separately the steps of (i) the synthesis of the colloids, (ii) their precipitation, and (iii) the drying of the resulting gel to understand the role of the ligands therein. ZnO particles only covered with acetate grow to 5 nm during the drying process, whereas particles with any of the additional ligands retain their colloidal size of 2–3 nm. This clearly shows the efficient binding and effect of the presented ligands.

  2. Synthesis of Copper Nanoparticles in Ethylene Glycol by Chemical Reduction with Vanadium (+2 Salts

    Directory of Open Access Journals (Sweden)

    Andrea Pietro Reverberi

    2016-09-01

    Full Text Available Copper nanoparticles have been synthesized in ethylene glycol (EG using copper sulphate as a precursor and vanadium sulfate as an atypical reductant being active at room temperature. We have described a technique for a relatively simple preparation of such a reagent, which has been electrolytically produced without using standard procedures requiring an inert atmosphere and a mercury cathode. Several stabilizing agents have been tested and cationic capping agents have been discarded owing to the formation of complex compounds with copper ions leading to insoluble phases contaminating the metallic nanoparticles. The elemental copper nanoparticles, stabilized with polyvinylpyrrolidone (PVP and sodium dodecyl sulphate (SDS, have been characterized for composition by energy dispersive X-ray spectroscopy (EDS, and for size by dynamic light scattering (DLS, and transmission electron microscopy (TEM, giving a size distribution in the range of 40–50 nm for both stabilizing agents. From a methodological point of view, the process described here may represent an alternative to other wet-chemical techniques for metal nanoparticle synthesis in non-aqueous media based on conventional organic or inorganic reductants.

  3. Collagen-chitosan scaffold modified with Au and Ag nanoparticles: Synthesis and structure

    Science.gov (United States)

    Rubina, M. S.; Kamitov, E. E.; Zubavichus, Ya. V.; Peters, G. S.; Naumkin, A. V.; Suzer, S.; Vasil'kov, A. Yu.

    2016-03-01

    Nowadays, the dermal biomimetic scaffolds are widely used in regenerative medicine. Collagen-chitosan scaffold one of these materials possesses antibacterial activity, good compatibility with living tissues and has been already used as a wound-healing material. In this article, collagen-chitosan scaffolds modified with Ag and Au nanoparticles have been synthesized using novel method - the metal-vapor synthesis. The nanocomposite materials are characterized by XPS, TEM, SEM and synchrotron radiation-based X-ray techniques. According to XRD data, the mean size of the nanoparticles (NPs) is 10.5 nm and 20.2 nm in Au-Collagen-Chitosan (Au-CollCh) and Ag-Collagen-Chitosan (Ag-CollCh) scaffolds, respectively in fair agreement with the TEM data. SAXS analysis of the composites reveals an asymmetric size distribution peaked at 10 nm for Au-CollCh and 25 nm for Ag-CollCh indicative of particle's aggregation. According to SEM data, the metal-carrying scaffolds have layered structure and the nanoparticles are rather uniformly distributed on the surface material. XPS data indicate that the metallic nanoparticles are in their unoxidized/neutral states and dominantly stabilized within the chitosan-rich domains.

  4. Synthesis of Silver and Gold Nanoparticles Using Antioxidants from Blackberry, Blueberry, Pomegranate, and Turmeric Extracts

    Science.gov (United States)

    Greener synthesis of Ag and Au nanoparticles is described using antioxidants from blackberry, blueberry, pomegranate, and turmeric extracts. The synthesized particles were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution TEM (HR...

  5. Polymeric nanoparticles: Recent development in synthesis and application

    Directory of Open Access Journals (Sweden)

    S. Mallakpour

    2016-11-01

    Full Text Available Nanosized particles have attractive characteristics, which have received considerable attention in the last decade. Polymeric nanoparticles (PNPs are solid particles or particulate dispersions with size in the range of 10–1000 nm. Due to the very small size, the surface area is very large so the percentage of atoms or molecules on the surface is significantly increased, which is expected to have extensive applications in various fields such as drug delivery systems, biosensors, catalysts, nanocomposites, agriculture and environment. The aim of the present paper is to critically review enhancement in the field of synthesis and different application of novel PNPs in various area from drug delivery to composite fabrication. Literature sources were mainly taken from the publications of 2011 and later; though, for a basic depiction of the structural principles, older publications have also been cited.

  6. Unveiling the chemistry behind the green synthesis of metal nanoparticles.

    Science.gov (United States)

    Santos, Sónia A O; Pinto, Ricardo J B; Rocha, Sílvia M; Marques, Paula A A P; Pascoal Neto, Carlos; Silvestre, Armando J D; Freire, Carmen S R

    2014-09-01

    Nanobiotechnology has emerged as a fundamental domain in modern science, and metallic nanoparticles (NPs) are one of the largest classes of NPs studied because of their wide spectrum of possible applications in several fields. The use of plant extracts as reducing and stabilizing agents in their synthesis is an interesting and reliable alternative to conventional methodologies. However, the role of the different components of such extracts in the reduction/stabilization of metal ions has not yet been understood clearly. Here we studied the behavior of the main components of a Eucalyptus globulus Labill. bark aqueous extract during metal-ion reduction followed by advanced chromatographic techniques, which allowed us to establish their specific role in the process. The obtained results showed that phenolic compounds, particularly galloyl derivatives, are mainly responsible for the metal-ion reduction, whereas sugars are essentially involved in the stabilization of the NPs.

  7. Synthesis and Antimicrobial Activity of Silver-Doped Hydroxyapatite Nanoparticles

    Directory of Open Access Journals (Sweden)

    Carmen Steluta Ciobanu

    2013-01-01

    Full Text Available The synthesis of nanosized particles of Ag-doped hydroxyapatite with antibacterial properties is of great interest for the development of new biomedical applications. The aim of this study was the evaluation of Ca10−xAgx(PO46(OH2 nanoparticles (Ag:HAp-NPs for their antibacterial and antifungal activity. Resistance to antimicrobial agents by pathogenic bacteria has emerged in the recent years and became a major health problem. Here, we report a method for synthesizing Ag doped nanocrystalline hydroxyapatite. A silver-doped nanocrystalline hydroxyapatite was synthesized at 100°C in deionised water. Also, in this paper Ag:HAp-NPs are evaluated for their antimicrobial activity against Gram-positive and Gram-negative bacteria and fungal strains. The specific antimicrobial activity revealed by the qualitative assay is demonstrating that our compounds are interacting differently with the microbial targets, probably due to the differences in the microbial wall structures.

  8. Magnetic Iron Oxide Nanoparticles: Synthesis and Surface Functionalization Strategies

    Directory of Open Access Journals (Sweden)

    He Quanguo

    2008-01-01

    Full Text Available Abstract Surface functionalized magnetic iron oxide nanoparticles (NPs are a kind of novel functional materials, which have been widely used in the biotechnology and catalysis. This review focuses on the recent development and various strategies in preparation, structure, and magnetic properties of naked and surface functionalized iron oxide NPs and their corresponding application briefly. In order to implement the practical application, the particles must have combined properties of high magnetic saturation, stability, biocompatibility, and interactive functions at the surface. Moreover, the surface of iron oxide NPs could be modified by organic materials or inorganic materials, such as polymers, biomolecules, silica, metals, etc. The problems and major challenges, along with the directions for the synthesis and surface functionalization of iron oxide NPs, are considered. Finally, some future trends and prospective in these research areas are also discussed.

  9. Towards the development of multifunctional chitosan-based iron oxide nanoparticles: Optimization and modelling of doxorubicin release.

    Science.gov (United States)

    Soares, Paula I P; Sousa, Ana Isabel; Ferreira, Isabel M M; Novo, Carlos M M; Borges, João Paulo

    2016-11-20

    In the present work composite nanoparticles with a magnetic core and a chitosan-based shell were produced as drug delivery systems for doxorubicin (DOX). The results show that composite nanoparticles with a hydrodynamic diameter within the nanometric range are able to encapsulate more DOX than polymeric nanoparticles alone corresponding also to a higher drug release. Moreover the synthesis method of the iron oxide nanoparticles influences the total amount of DOX released and a high content of iron oxide nanoparticles inhibits DOX release. The modelling of the experimental results revealed a release mechanism dominated by Fickian diffusion.

  10. Synthesis of silica based porous nanomaterials

    Science.gov (United States)

    Mueller, Paul S.

    Silica is one of the most abundant elements on the planet, has flexible bonding properties and generally excellent stability. Because of these properties, silica has been a vital component in technologies ranging from ancient glassware to modern supercomputers. Silica is able to form a wide range of materials both alone and as a component of larger material frameworks. Porous silica based nanomaterials are rapidly growing in importance because of their many applications in a wide variety of fields. This thesis focuses on the synthesis of silica based porous nanomaterials: nanocrystalline zeolites, mesoporous silica nanoparticles, and iron oxide core/shell nanocomposites. The synthetic conditions of these materials were varied in order to maximize efficiency, minimize environmental impact, and produce high quality material with far reaching potential applications. The materials were characterized by physicochemical techniques including Transmission Electron Microscopy, Dynamic Light Scattering, Powder X-Ray Diffraction, Solid State NMR, and Nitrogen Adsorption Isotherms. The materials were evaluated and conditions were controlled to produce high yields of quality nanomaterials and hypothesize methods for further synthetic control. The products will be used in studies involving nanoparticle toxicity, environmental remediation, and drug delivery.

  11. Antimicrobial property of zinc based nanoparticles

    Science.gov (United States)

    Chiriac, V.; Stratulat, D. N.; Calin, G.; Nichitus, S.; Burlui, V.; Stadoleanu, C.; Popa, M.; Popa, I. M.

    2016-06-01

    Pathogen bacteria strains with wide spectrum can cause serious infections with drastic damages on humans. There are studies reflecting antibacterial effect of nanoparticles type metal or metal oxides as an alternative or concurrent treatment to the diseases caused by infectious agents. Synthesised nanoparticles using different methods like sol-gel, hydrothermal or plant extraction were tested following well-established protocols with the regard to their antimicrobial activity. It was found that zinc based nanoparticles possess strong synergistic effect with commonly used antibiotics on infection tratment.

  12. Development and Antibacterial Activity of Cashew Gum-Based Silver Nanoparticles

    Directory of Open Access Journals (Sweden)

    Maria José dos S. Soares

    2013-03-01

    Full Text Available The present study describes the development of a green synthesis of silver nanoparticles reduced and stabilized by exuded gum from Anacardium occidentale L. and evaluates in vitro their antibacterial and cytotoxic activities. Characterization of cashew gum-based silver nanoparticles (AgNPs was carried out based on UV–Vis spectroscopy, transmission electron microscopy and dynamic light scattering analysis which revealed that the synthesized silver nanoparticles were spherical in shape, measuring about 4 nm in size with a uniform dispersal. AgNPs presented antibacterial activity, especially against Gram-negative bacteria, in concentrations where no significant cytotoxicity was observed.

  13. Solvothermal synthesis and analysis of Bi{sub 1-x}Sb{sub x} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Sumithra, S.; Misra, D.K.; Wei, C. [Advanced Materials Research Institute, University of New Orleans, New Orleans, LA 70148 (United States); Gabrisch, H. [GKSS Research Center, Institute of Materials Research, Geesthacht (Germany); Poudeu, P.F.P. [Advanced Materials Research Institute, University of New Orleans, New Orleans, LA 70148 (United States); Department of Chemistry, University of New Orleans, New Orleans, LA 70148 (United States); Stokes, K.L., E-mail: klstokes@uno.edu [Advanced Materials Research Institute, University of New Orleans, New Orleans, LA 70148 (United States); Department of Physics, University of New Orleans, New Orleans, LA 70148 (United States)

    2011-02-25

    Bismuth-antimony alloy nanoparticles have been synthesized by a facile solvothermal method using N,N-dimethylformamide and ethylene glycol as solvent/reducing agent; BiCl{sub 3}, SbCl{sub 3} and Bi(NO{sub 3}){sub 3} as precursors; and citric acid as a surface modifier/stabilizing agent. The particle size and size distribution of Bi nanoparticles were analyzed as a function of the synthesis conditions: molar ratio of precursor to surfactant, precursor concentration and reducing agent. Synthesis of Sb and Bi{sub 0.88}Sb{sub 0.12} under similar conditions was also investigated. The phase purity of nanoparticles was confirmed from X-ray diffraction and thermogravimetry and the nanoparticle morphology was investigated by transmission electron microscopy. A case study of Bi nanoparticles with detailed analysis of the particle morphology and size distribution of the nanoparticles is reported.

  14. Efficient synthesis of silver nanoparticles from Prosopis juliflora leaf extract and its antimicrobial activity using sewage

    Science.gov (United States)

    Raja, K.; Saravanakumar, A.; Vijayakumar, R.

    2012-11-01

    In this paper, aqueous extract of fresh leaves of Prosopis juliflora was used for the synthesis of silver (Ag) nanoparticles. UV-Vis spectroscopy studies were carried out to asses silver nanoparticles formation within 5 min, scanning electron microscopic was used to characterize shape of the Ag nanoparticles, X-ray diffraction analysis confirms the nanoparticles as crystalline silver and facecentered cubic type and Fourier transform infra-red assed that shows biomolecule compounds which are responsible for reduction and capping material of silver nanoparticles. The anti microbial activity of silver nanoparticle was performed using sewage. The approach of plant-mediated synthesis appears to be cost efficient, eco-friendly and easy methods.

  15. Synthesis of silver nanoparticles by using tea leaf extract from Camellia sinensis.

    Science.gov (United States)

    Loo, Yuet Ying; Chieng, Buong Woei; Nishibuchi, Mitsuaki; Radu, Son

    2012-01-01

    The development of the biological synthesis of nanoparticles using microorganisms or plant extracts plays an important role in the field of nanotechnology as it is environmentally friendly and does not involve any harmful chemicals. In this study, the synthesis of silver nanoparticles using the leaves extract of Chinese tea from Camellia sinensis is reported. The synthesized nanoparticles were characterized using UV-vis spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared (FTIR) spectroscopy. The XRD analysis shows that the synthesized silver nanoparticles are of face-centered cubic structure. Well-dispersed silver nanoparticles with an approximate size of 4 nm were observed in the TEM image. The application of the green synthesized nanoparticles can be used in many fields such as cosmetics, foods, and medicine. PMID:22904632

  16. Antibacterial Properties of Copper Nanoparticle Dispersions: Influence of Synthesis Conditions and Physicochemical Characteristics

    Science.gov (United States)

    Godymchuk, A.; Frolov, G.; Gusev, A.; Zakharova, O.; Yunda, E.; Kuznetsov, D.; Kolesnikov, E.

    2015-11-01

    The production of bactericidal plasters, bandages and medicines with the inclusion of copper nanoparticles and copper ions may have a great potential in terms of their biomedical application. The work considers the influence of the synthesis conditions, size, aggregation status, and charge of nanoparticles in aqueous solutions as well as the type of microorganisms to the antibacterial properties of water suspensions of electroexplosive copper nanoparticles in the conditions in vitro in relation to strains Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus cereus. Water dispersions of copper nanoparticles were shown to inhibit the growth of test cells for both G+ and G- microbacteria but the degree of such an influence strongly depended on the type of a test strain. The authors have demonstrated that use of deeply purified water and alcohol-containing stabilizers at the synthesis of nanoparticles via metals electric erosion in the liquid prevents the copper nanoparticles coagulation and significantly influences on their physicochemical characteristics and, consequently, antibacterial properties.

  17. Silver Nanoparticles: Synthesis, Characterization, Properties, Applications, and Therapeutic Approaches

    Science.gov (United States)

    Zhang, Xi-Feng; Liu, Zhi-Guo; Shen, Wei; Gurunathan, Sangiliyandi

    2016-01-01

    Recent advances in nanoscience and nanotechnology radically changed the way we diagnose, treat, and prevent various diseases in all aspects of human life. Silver nanoparticles (AgNPs) are one of the most vital and fascinating nanomaterials among several metallic nanoparticles that are involved in biomedical applications. AgNPs play an important role in nanoscience and nanotechnology, particularly in nanomedicine. Although several noble metals have been used for various purposes, AgNPs have been focused on potential applications in cancer diagnosis and therapy. In this review, we discuss the synthesis of AgNPs using physical, chemical, and biological methods. We also discuss the properties of AgNPs and methods for their characterization. More importantly, we extensively discuss the multifunctional bio-applications of AgNPs; for example, as antibacterial, antifungal, antiviral, anti-inflammatory, anti-angiogenic, and anti-cancer agents, and the mechanism of the anti-cancer activity of AgNPs. In addition, we discuss therapeutic approaches and challenges for cancer therapy using AgNPs. Finally, we conclude by discussing the future perspective of AgNPs. PMID:27649147

  18. Radiolytic Synthesis of Colloidal Silver Nanoparticles for Antibacterial Wound Dressings

    Directory of Open Access Journals (Sweden)

    Pimpon Uttayarat

    2015-01-01

    Full Text Available Radiolytic synthesis provides a convenient and environmentally-friendly approach to prepare metallic nanoparticles in large scale with narrow size distribution. In this report, colloidal silver nanoparticles (AgNPs were synthesized by gamma radiation using poly(vinyl alcohol (PVA or silk fibroin (SF as stabilizers and were evaluated for their antibacterial properties. The conversion of metallic silver ions to silver atoms depended on irradiation dose and stabilizer concentration as determined by UV-Vis spectrophotometry and transmission electron microscopy. The uniformly dispersed AgNPs with diameter 32.3 ± 4.40 nm were evaluated as antiseptic agents in films composed of chitosan, SF, and PVA that were processed by irradiation-induced crosslinking. Using disc diffusion assay, the films containing 432 ppm AgNPs could effectively inhibit the growth of both Staphylococcus aureus and Pseudomonas aeruginosa. Therefore, we have demonstrated in our present study that gamma radiation technique can potentially be applied in the mass production of antibacterial wound dressings.

  19. Trichosporon jirovecii-mediated synthesis of cadmium sulfide nanoparticles.

    Science.gov (United States)

    El-Baz, Ashraf Farag; Sorour, Noha Mohamed; Shetaia, Youssria Mohamed

    2016-05-01

    Cadmium sulphide is one of the most promising materials for solar cells and of great interest due to its useful applications in photonics and electronics, thus the development of bio-mediated synthesis of cadmium sulphide nanoparticles (CdS NPs) is one of the essential areas in nanoparticles. The present study demonstrates for the first time the eco-friendly biosynthesis of CdS NPs using the yeast Trichosporon jirovecii. The biosynthesis of CdS NPs were confirmed by UV-Vis spectrum and characterized by X-ray diffraction assay and electron microscopy. Scanning and transmission electron microscope analyses shows the formation of spherical CdS NPs with a size range of about 6-15 nm with a mean Cd:S molar ratio of 1.0:0.98. T. jirovecii produced hydrogen sulfide on cysteine containing medium confirmed by positive cysteine-desulfhydrase activity and the colony color turned yellow on 0.1 mM cadmium containing medium. T. jirovecii tolerance to cadmium was increased by the UV treatment and three 0.6 mM cadmium tolerant mutants were generated upon the UV radiation treatment. The overall results indicated that T. jirovecii could tolerate cadmium toxicity by its conversion into CdS NPs on cysteine containing medium using cysteine-desulfhydrase as a defense response mechanism. PMID:26467054

  20. Silver Nanoparticles: Synthesis, Characterization, Properties, Applications, and Therapeutic Approaches.

    Science.gov (United States)

    Zhang, Xi-Feng; Liu, Zhi-Guo; Shen, Wei; Gurunathan, Sangiliyandi

    2016-01-01

    Recent advances in nanoscience and nanotechnology radically changed the way we diagnose, treat, and prevent various diseases in all aspects of human life. Silver nanoparticles (AgNPs) are one of the most vital and fascinating nanomaterials among several metallic nanoparticles that are involved in biomedical applications. AgNPs play an important role in nanoscience and nanotechnology, particularly in nanomedicine. Although several noble metals have been used for various purposes, AgNPs have been focused on potential applications in cancer diagnosis and therapy. In this review, we discuss the synthesis of AgNPs using physical, chemical, and biological methods. We also discuss the properties of AgNPs and methods for their characterization. More importantly, we extensively discuss the multifunctional bio-applications of AgNPs; for example, as antibacterial, antifungal, antiviral, anti-inflammatory, anti-angiogenic, and anti-cancer agents, and the mechanism of the anti-cancer activity of AgNPs. In addition, we discuss therapeutic approaches and challenges for cancer therapy using AgNPs. Finally, we conclude by discussing the future perspective of AgNPs. PMID:27649147

  1. Synthesis of 1 nm Pd Nanoparticles in a Microfluidic Reactor: Insights from in Situ X ray Absorption Fine Structure Spectroscopy and Small-Angle X ray Scattering

    Energy Technology Data Exchange (ETDEWEB)

    Karim, Ayman M.; Al Hasan, Naila M.; Ivanov, Sergei A.; Siefert, Soenke; Kelly, Ryan T.; Hallfors, Nicholas G.; Benavidez, Angelica D.; Kovarik, Libor; Jenkins, Aaron; Winans, R. E.; Datye, Abhaya K.

    2015-06-11

    In this paper we show that the temporal separation of nucleation and growth is not a necessary condition for the colloidal synthesis of monodisperse nanoparticles. The synthesis mechanism of Pd nanoparticles was determined by in situ XAFS and SAXS in a microfluidic reactor capable of millisecond up to an hour time resolution. The SAXS results showed two autocatalytic growth phases, a fast growth phase followed by a very slow growth phase. The steady increase in the number of particles throughout the two growth phases indicates the synthesis is limited by slow continuous nucleation. The transition from fast to slow growth was caused by rapid increase in bonding with the capping agent as shown by XAFS. Based on this fundamental understanding of the synthesis mechanism, we show that 1 nm monodisperse Pd nanoparticles can be synthesized at low temperature using a strong binding capping agent such as trioctylphosphine (TOP).

  2. In-situ synthesis of nanoparticles via supersolubilizing micelle self-assembly

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    In-situ synthesis of nano-particles using the self-assembly of molten salt and super soluble micellae was proposed based on a phenomenon of super solubilization of molten salt in reverse micellae and its self-assembly when the concentration reached up to 95%(w/w).The mechanism of the self-assembly indicates that the self-assembly of molten salt occurs in a reverse micelle where a homogenous phase is established between 5%(w/w)of a surfactant with a VB value of less than 1 and a hydrocarbon spe- cies.This synthesis has some unique features,such as being free of water,highly effective deposition and narrow distribution of particle size.

  3. In-situ synthesis of nanoparticles via supersolubilizing micelle self-assembly

    Institute of Scientific and Technical Information of China (English)

    WANG DingCong

    2007-01-01

    In-situ synthesis of nano-particles using the self-assembly of molten salt and super soluble micellae was proposed based on a phenomenon of super solubilization of molten salt in reverse micellae and its self-assembly when the concentration reached up to 95% (w/w). The mechanism of the self-assembly indicates that the self-assembly of molten salt occurs in a reverse micelle where a homogenous phase is established between 5% (w/w) of a surfactant with a VB value of less than 1 and a hydrocarbon species. This synthesis has some unique features, such as being free of water, highly effective deposition and narrow distribution of particle size.

  4. Synthesis of mesoporous zeolite catalysts by in situ formation of carbon template over nickel nanoparticles

    DEFF Research Database (Denmark)

    Abildstrøm, Jacob Oskar; Kegnæs, Marina; Hytoft, Glen;

    2016-01-01

    A novel synthesis procedure for the preparation of the hierarchical zeolite materials with MFI structure based on the carbon templating method with in situ generated carbon template is presented in this study. Through chemical vapour deposition of coke on nickel nanoparticles supported on silica...... oxide, a carbon-silica composite is obtained and exploited as a combined carbon template/silica source for zeolite synthesis. This approach has several advantages in comparison with conventional carbon templating methods, where relatively complicated preparative strategies involving multistep...... impregnation procedures and rather expensive chemicals are used. Removal of the carbon template by combustion results in zeolite single crystals with intracrystalline pore volumes between 0.28 and 0.48 cm3/g. The prepared zeolites are characterized by XRD, SEM, TEM and physisorption analysis. The isomerization...

  5. Recent Trends in the Microwave-Assisted Synthesis of Metal Oxide Nanoparticles Supported on Carbon Nanotubes and Their Applications

    Directory of Open Access Journals (Sweden)

    Sarah C. Motshekga

    2012-01-01

    Full Text Available The study of coating carbon nanotubes with metal/oxides nanoparticles is now becoming a promising and challenging area of research. To optimize the use of carbon nanotubes in various applications, it is necessary to attach functional groups or other nanostructures to their surface. The combination of the distinctive properties of carbon nanotubes and metal/oxides is expected to be applied in field emission displays, nanoelectronic devices, novel catalysts, and polymer or ceramic reinforcement. The synthesis of these composites is still largely based on conventional techniques, such as wet impregnation followed by chemical reduction of the metal nanoparticle precursors. These techniques based on thermal heating can be time consuming and often lack control of particle size and morphology. Hence, there is interest in microwave technology recently, where using microwaves represents an alternative way of power input into chemical reactions through dielectric heating. This paper covers the synthesis and applications of carbon-nanotube-coated metal/oxides nanoparticles prepared by a microwave-assisted method. The reviewed studies show that the microwave-assisted synthesis of the composites allows processes to be completed within a shorter reaction time with uniform and well-dispersed nanoparticle formation.

  6. Mild Hydrothermal Synthesis of Ni–Cu Nanoparticles

    Directory of Open Access Journals (Sweden)

    G. H. Mohamed Saeed

    2010-01-01

    Full Text Available Magnetic Ni-rich Ni–Cu nanoparticles with Ni : Cu mass ratio (S of 2.0 and 2.6 were prepared using a mixture of polyoxyethylene (10 isooctylphenyl ether (Triton X-100 and sodium dodecyl sulfate (SDS in a mild hydrothermal condition at 95ºC. X-ray diffractometry (XRD showed that the nanoparticles prepared at S=2.0 possessed Ni–Cu alloy characteristic whereas the characteristic was absent at S=2.6. The XRD data was enhanced by Fourier transform infrared spectroscopy (FTIR which exhibited metal-metal (Ni–Cu band at 455 cm−1. Based on transmission electron microscopy (TEM, the average particle sizes for the nanoparticles prepared at S=2.0 and 2.6 were in the range of 19–23 nm. The as-prepared nanoparticles exhibited paramagnetic behaviour measured using a vibrating sample magnetometer (VSM and the specific saturation magnetization decreased at the higher concentration of Ni.

  7. Preparation of novel core-shell nanoparticles by electrochemical synthesis

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Nanostructural gold/polyaniline core/shell composite particles on conducting electrode ITO were successfully prepared via electrochemical polymerization of aniline based on 4-aminothiophenol (4-ATP) capped Au nanoparticles. The new approach to the fabrication included three steps: preparation of gold nanoparticles as core by pulse electrodeposition; formation of ATP monolayer on the gold particle surface, which served as a binder and an initiator; polymerization of aniline monomer initiated by ATP molecules under controlled voltage lower than the voltammetric threshold of aniline polymerization, which assured the formation of polyaniline shell film occurred on gold particles selectively. Topographic images were also studied by AFM, which indicated the diameter of gold nanoparticles were around 250 nm. Coulometry characterization confirmed the shell thickness of polyaniline film was about 30 nm.A possible formation mechanism of the Au/polyaniline core-shell nanocomposites was also proposed. The novel as-prepared core-shell nanoparticles have potential application in constructing biosensor when bioactive enzymes are absorbed or embedded in polyaniline shell film.

  8. Synthesis of photoactive AgCl/SBA-15 by conversion of silver nanoparticles into stable AgCl nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zienkiewicz-Strzalka, M., E-mail: gosiazienkiewicz@wp.pl [Department of Crystallography, Faculty of Chemistry, Maria Curie-Sklodowska University, sq. Maria Curie-Sklodowska 3, 20-031 Lublin (Poland); Pikus, S. [Department of Crystallography, Faculty of Chemistry, Maria Curie-Sklodowska University, sq. Maria Curie-Sklodowska 3, 20-031 Lublin (Poland)

    2013-01-15

    Highlights: Black-Right-Pointing-Pointer A new material AgCl/SBA-15 was synthesized and characterized. Black-Right-Pointing-Pointer New simple and effective approach of preparation was proposed. Black-Right-Pointing-Pointer AgCl/SBA-15 material was tested as an active agent during photodegradation of phenol and its photoactivity was confirmed. Black-Right-Pointing-Pointer The photoactive properties depend on AgCl nanoparticles present in the composite. - Abstract: In this work the results of synthesis the ordered mesoporous silica (SBA-15) in the presence of stable silver nanoparticles were presented. It has been proven that the proposed method leads to the synthesis of SBA-15 nanocomposite containing silver chloride nanoparticles, formed by the transformation of silver nanoparticles in the acidic conditions. Proposed one-pot procedure is simple and the one requirement is to prepare a stable solution of silver nanoparticles. In this work, silver nanoparticles were obtained during chemical reduction of [Ag(NH{sub 3}){sub 2}]{sup +} ions by formaldehyde. Silver nanoparticles solution can be used as a silver chloride source due to the application of the same polymer as a stabilizer of nanocrystals and structure directing agent of SBA-15. The final AgCl/SBA-15 materials show excellent structural ordering characteristic for this type of materials confirmed by diffraction measurements in range of small angles 2{theta}, transmission electron microscopy (TEM) and nitrogen adsorption/desorption measurements. AgCl nanoparticles were identified by diffraction measurements as chlorargyrite phase. The presence of silver nanoparticles in initial solution and their absence after synthesis were confirmed by UV-vis measurements. The photoactivity of obtained AgCl/SBA-15 composite was tested in reaction of organic impurities photodegradation.

  9. Fungi as an efficient mycosystem for the synthesis of metal nanoparticles: progress and key aspects of research.

    Science.gov (United States)

    Yadav, Alka; Kon, Kateryna; Kratosova, Gabriela; Duran, Nelson; Ingle, Avinash P; Rai, Mahendra

    2015-11-01

    Nanotechnology is an emerging cutting-edge technology, which involves interdisciplinary subjects, such as physics, chemistry, biology, material science and medicine. Different methods for the synthesis of nanoparticles have been discussed here. Although physical and chemical methods have been successfully used to synthesize nanoparticles, the use of hazardous chemicals and synthesis at high temperature is a matter of concern. Hence, there is a necessity to develop eco-friendly techniques for the synthesis of nanoparticles. Biosynthesis of nanoparticles by fungi, bacteria, actinomycetes, lichen and viruses have been reported eco-friendly. Moreover, the fungal system has emerged as an efficient system for nanoparticle synthesis as fungi possess distinctive characters including high wall binding capacity, easy to culture and simpler biomass handling, etc. In this review, we have discussed fungi as an important tool for the fabrication of nanoparticles. In addition, methods and mechanism for synthesis of nanoparticles and its potential applications have also been discussed. PMID:26164702

  10. Endophytic synthesis of silver chloride nanoparticles from Penicillium sp. of Calophyllum apetalum

    Science.gov (United States)

    Chandrappa, C. P.; Govindappa, M.; Chandrasekar, N.; Sarkar, Sonia; Ooha, Sepuri; Channabasava, R.

    2016-06-01

    In the present study, Penicillium species extract isolated from Calophyllum apetalum was used for the synthesis of silver nanoparticles and it was confirmed by changing the color of the silver nitrate UV-Vis spectrum. The synthesized nanoparticles have been characterized by biophysical techniques such as scanning electron microscopy and x-ray diffraction.

  11. Surfactant-free synthesis of mesoporous and hollow silica nanoparticles with an inorganic template.

    Science.gov (United States)

    Baù, Luca; Bártová, Barbora; Arduini, Maria; Mancin, Fabrizio

    2009-12-28

    A surfactant-free synthesis of mesoporous and hollow silica nanoparticles is reported in which boron acts as the templating agent. Using such a simple and mild procedure as a treatment with water, the boron-rich phase is selectively removed, affording mesoporous pure silica nanoparticles with wormhole-like pores or, depending on the synthetic conditions, silica nanoshells. PMID:20024287

  12. Synthesis and Catalytic Evaluation of Dendrimer-Encapsulated Cu Nanoparticles: An Undergraduate Experiment Exploring Catalytic Nanomaterials

    Science.gov (United States)

    Feng, Z. Vivian; Lyon, Jennifer L.; Croley, J. Sawyer; Crooks, Richard M.; Vanden Bout, David A.; Stevenson, Keith J.

    2009-01-01

    Copper nanoparticles were synthesized using generation 4 hydroxyl-terminated (G4-OH) poly(amidoamine) (PAMAM) dendrimers as templates. The synthesis is conducted by coordinating copper ions with the interior amines of the dendrimer, followed by chemical reduction to form dendrimer-encapsulated copper nanoparticles (Cu-DEN). The catalytic…

  13. Synthesis and characterization of biodegradable lignin nanoparticles with tunable surface properties

    NARCIS (Netherlands)

    Richter, Alexander P.; Bharti, Bhuvnesh; Armstrong, Hinton B.; Brown, Joseph S.; Plemmons, Dayne; Paunov, Vesselin N.; Stoyanov, Simeon D.; Velev, Orlin D.

    2016-01-01

    Lignin nanoparticles can serve as biodegradable carriers of biocidal actives with minimal environmental footprint. Here we describe the colloidal synthesis and interfacial design of nanoparticles with tunable surface properties using two different lignin precursors, Kraft (Indulin AT) lignin and

  14. Effect on nerve structures of functionalized gold-chitosan nanoparticles obtained by one pot synthesis

    Directory of Open Access Journals (Sweden)

    Marius Dobromir

    2011-02-01

    Full Text Available Gold nanoparticles have potential applications in drug delivery, cancer diagnosis and therapy, food industry and environment remediation. However, little is known about their potential toxicity or fate in the environment. In this study we observed significant effects of functionalized gold-chitosan nanoparticles obtained by one pot synthesis on nerve structures of Wistar rats.

  15. Magnetite Fe3O4 nanoparticles synthesis by wet chemical reduction and their characterization

    Science.gov (United States)

    Chaki, S. H.; Malek, Tasmira J.; Chaudhary, M. D.; Tailor, J. P.; Deshpande, M. P.

    2015-09-01

    The authors report the synthesis of Fe3O4 nanoparticles by wet chemical reduction technique at ambient temperature and its characterization. Ferric chloride hexa-hydrate (FeCl3 · 6H2O) and sodium boro-hydrate (NaBH4) were used for synthesis of Fe3O4 nanoparticles at ambient temperature. The elemental composition of the synthesized Fe3O4 nanoparticles was determined by energy dispersive analysis of x-rays technique. The x-ray diffraction (XRD) technique was used for structural characterization of the nanoparticles. The crystallite size of the nanoparticles was determined using XRD data employing Scherrer’s formula and Hall-Williamson’s plot. Surface morphology of as-synthesized Fe3O4 nanoparticles was studied by scanning electron microscopy. High resolution transmission electron microscopy analysis of the as-synthesized Fe3O4 nanoparticles showed narrow range of particles size distribution. The optical absorption of the synthesized Fe3O4 nanoparticles was studied by UV-vis-NIR spectroscopy. The as-synthesized nanoparticles were analyzed by Fourier transform infrared spectroscopy technique for absorption band study in the infrared region. The magnetic properties of the as-synthesized Fe3O4 nanoparticles were evaluated by vibrating sample magnetometer technique. The thermal stability of the as-synthesized Fe3O4 nanoparticles was studied by thermogravimetric technique. The obtained results are elaborated and discussed in details in this paper.

  16. Generic Biocombinatorial Strategy to Select Tailor-Made Stabilizers for Sol-Gel Nanoparticle Synthesis.

    Science.gov (United States)

    Hanßke, Felix; Kemnitz, Erhard; Börner, Hans G

    2015-09-01

    A generic route for the selection of nanoparticle stabilizers via biocombinatorial means of phage display peptide screening is presented, providing magnesium fluoride nanoparticle synthesis as example. Selected sequence-specific MgF2 binders are evaluated for their adsorption behavior. Peptide-polymer conjugates derived from the best binding peptide are used for the stabilization of MgF2 sol nanoparticles, yielding fully redispersable dry states and improoving processability significantly.

  17. Metallic ruthenium nanoparticles derived from arene ruthenium complexes: synthesis, characterization and applications

    OpenAIRE

    Khan, Farooq-Ahmad; Süss-Fink, Georg

    2012-01-01

    The present work deals with the preparation of ruthenium nanoparticles using an organometallic approach. In the first part, the synthesis of ruthenium nanoparticles stabilized by mesogenic isonicotinic ester ligands is presented. We have been interested in the use of long-chain isonicotinic esters as lipohilic components in order to increase the anticancer activity of arene ruthenium complexes, while using them as stabilizers for ruthenium nanoparticles with the aim of exploring self-organiz...

  18. Synthesis and optimization of chitosan nanoparticles: Potential applications in nanomedicine and biomedical engineering

    OpenAIRE

    Ghadi, Arezou; Mahjoub, Soleiman; Tabandeh, Fatemeh; Talebnia, Farid

    2014-01-01

    Background: Chitosan nanoparticles have become of great interest for nanomedicine, biomedical engineering and development of new therapeutic drug release systems with improved bioavailability, increased specificity and sensitivity, and reduced pharmacological toxicity. The aim of the present study was to synthesis and optimize of the chitosan nanoparticles for industrial and biomedical applications. Methods: Fe3O4 was synthesized and optimized as magnetic core nanoparticles and then chitosan ...

  19. SYNTHESIS AND CHARACTERIZATION OF PLANT – MEDIATED SILVER NANOPARTICLES FROM CANARIUM STRICTUM ROXB. MESOCARP EXTRACT

    Directory of Open Access Journals (Sweden)

    A.KALA1, S.SOOSAIRAJ1*, S.MATHIYAZHAGAN2 AND P.RAJA1

    2014-06-01

    Full Text Available In this study, we describe a cost effective and environment friendly technique for the biosynthesis of silver nanoparticles from 1mM AgNO3 solution through the extract of mesocarp of Canarium strictum as reducing agent. UV–visible spectroscopy was used for quantification of silver nanoparticle synthesis. The synthesized silver nanoparticles were characterized with Scanning electron microscopy (SEM and Fourier Transform Infrared Spectroscopy (FTIR.

  20. Synthesis and Biomedical Applications of Copper Sulfide Nanoparticles: From Sensors to Theranostics

    OpenAIRE

    Goel, Shreya; Chen, Feng; Cai, Weibo

    2013-01-01

    Copper sulfide (CuS) nanoparticles have attracted increasing attention from biomedical researchers across the globe, because of their intriguing properties which have been mainly explored for energy- and catalysis-related applications to date. This focused review article aims to summarize the recent progress made in the synthesis and biomedical applications of various CuS nanoparticles. After a brief introduction to CuS nanoparticles in the first section, we will provide a concise outline of ...

  1. Green Synthesis of Gold and Silver Nanoparticles Using Averrhoa bilimbi Fruit Extract

    OpenAIRE

    R. S. Rimal Isaac; Sakthivel, G.; Ch. Murthy

    2013-01-01

    We report on rapid one-step green synthesis of gold and silver nanoparticles using fruit extract of Averrhoa bilimbi Linn. UV-Vis absorption spectroscopy was used to monitor the quantitative formation of gold and silver nanoparticles. The characteristics of the obtained gold and silver nanoparticles were studied using UV-Vis absorption spectroscopy (UV/Vis), Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), and Energy-dispersive spectroscopy (EDX). UV/Vis spe...

  2. SYNTHESIS AND CHARACTERIZATION OF PLANT – MEDIATED SILVER NANOPARTICLES FROM CANARIUM STRICTUM ROXB. MESOCARP EXTRACT

    OpenAIRE

    A.KALA1, S.SOOSAIRAJ1*, S.MATHIYAZHAGAN2 AND P.RAJA1

    2014-01-01

    In this study, we describe a cost effective and environment friendly technique for the biosynthesis of silver nanoparticles from 1mM AgNO3 solution through the extract of mesocarp of Canarium strictum as reducing agent. UV–visible spectroscopy was used for quantification of silver nanoparticle synthesis. The synthesized silver nanoparticles were characterized with Scanning electron microscopy (SEM) and Fourier Transform Infrared Spectroscopy (FTIR).

  3. Microwave-assisted ionic-liquid-based synthesis of highly crystalline CaMoO4:RE3+ (RE = Tb, Sm, Eu) and Y2Mo4O15:Eu3+ nanoparticles

    Science.gov (United States)

    Kuzmanoski, Ana; Pankratov, Vladimir; Feldmann, Claus

    2015-03-01

    Fluorescent CaMoO4:RE3+ (RE = Tb, Sm, Eu) nanoparticles, 50-70 nm in diameter, were prepared via a microwave-assisted synthesis in ionic liquids. Herein, the ionic liquid allows heating to high temperatures in the liquid phase (200 °C), which guarantees for an optimal crystallization of the nanoparticles. All nanoparticles were indeed readily crystalline without the need of any additional powder sintering. Especially, CaMoO4:Tb and CaMoO4:Eu exhibit high quantum yields of 52% and 82% under UV-excitation (300-320 nm). All compounds were characterized by electron microscopy (SEM), dynamic light scattering (DLS), infrared spectroscopy (FT-IR), energy-dispersive X-ray analysis (EDX), X-ray diffraction (XRD), and fluorescence spectroscopy (FL). In order to shift the excitation to even higher wavelengths, Y2Mo4O15:Eu was firstly realized as a nanomaterial, again, using the microwave-assisted synthesis in ionic liquids. Y2Mo4O15:Eu exhibits a particle size of 25-30 nm, and shows a high quantum yield of 67%, too. As this nanomaterial can be excited up to 400 nm, it represents one of the first efficient red-emitting, Eu3+-doped nanomaterials for near-UV excitation (>350 nm) with a simple, low-cost UV-LED. This can be relevant for all kinds of thin-film applications as well as for optical imaging.

  4. Synthesis, photophysical properties and application of dye doped water soluble silica-based nanoparticles to label bacteria E. coli O157:H7

    International Nuclear Information System (INIS)

    Organically modified silicate (ORMOSIL) nanoparticles (NPs) doped with rhodamine 6G and rhodamine B (RB) dyes were synthesized by Stöber method from methyltriethoxysilane CH3Si(OCH3)3 precursor (MTEOS). The NPs are surface functionalized by cationic amino groups. The optical characterization of dye-doped ORMOSIL NPs was studied in comparison with that of free dye in solution. The synthesized NPs were used for labeling bacteria E. coli O157:H7. The number of bacteria have been counted using the fluorescent spectra and microscope images of labeled bacteria. The results show the ability of NPs to work as biomarkers. (paper)

  5. Green Chemistry Approach for Synthesis of Effective Anticancer Palladium Nanoparticles.

    Science.gov (United States)

    Gurunathan, Sangiliyandi; Kim, EunSu; Han, Jae Woong; Park, Jung Hyun; Kim, Jin-Hoi

    2015-12-15

    The purpose of this study was to design and synthesize Palladium nanoparticles (PdNPs) using an environmentally friendly approach and evaluate the in vitro efficacy of PdNPs in human ovarian cancer A2780 cells. Ultraviolet-Visible (UV-Vis) spectroscopy was used to monitor the conversion of Pd(II) ions to Pd(0)NPs. X-ray diffraction (XRD) revealed the crystallinity of the as-synthesized PdNPs and Fourier transform infrared spectroscopy (FTIR) further confirmed the role of the leaf extract of Evolvulus alsinoides as a reducing and stabilizing agent for the synthesis of PdNPs. Dynamic light scattering (DLS) and transmission electron microscopy (TEM) showed that the average size of the NPs was 5 nm. After a 24-h exposure to PdNPs, cell viability and light microscopy assays revealed the dose-dependent toxicity of the PdNPs. Furthermore, the dose-dependent cytotoxicity of the PdNPs was confirmed by lactate dehydrogenase (LDH), increased reactive oxygen species (ROS) generation, activation of PdNPs-induced autophagy, impairment of mitochondrial membrane potential (MMP), enhanced caspase-3 activity, and detection of TUNEL-positive cells. Our study demonstrates a single, simple, dependable and green approach for the synthesis of PdNPs using leaf extracts of Evolvulus alsinoides. Furthermore, the in vitro efficacy of PdNPs in human ovarian cancer cells suggests that it could be an effective therapeutic agent for cancer therapy.

  6. Green Chemistry Approach for Synthesis of Effective Anticancer Palladium Nanoparticles

    Directory of Open Access Journals (Sweden)

    Sangiliyandi Gurunathan

    2015-12-01

    Full Text Available The purpose of this study was to design and synthesize Palladium nanoparticles (PdNPs using an environmentally friendly approach and evaluate the in vitro efficacy of PdNPs in human ovarian cancer A2780 cells. Ultraviolet-Visible (UV-Vis spectroscopy was used to monitor the conversion of Pd(II ions to Pd(0NPs. X-ray diffraction (XRD revealed the crystallinity of the as-synthesized PdNPs and Fourier transform infrared spectroscopy (FTIR further confirmed the role of the leaf extract of Evolvulus alsinoides as a reducing and stabilizing agent for the synthesis of PdNPs. Dynamic light scattering (DLS and transmission electron microscopy (TEM showed that the average size of the NPs was 5 nm. After a 24-h exposure to PdNPs, cell viability and light microscopy assays revealed the dose-dependent toxicity of the PdNPs. Furthermore, the dose-dependent cytotoxicity of the PdNPs was confirmed by lactate dehydrogenase (LDH, increased reactive oxygen species (ROS generation, activation of PdNPs-induced autophagy, impairment of mitochondrial membrane potential (MMP, enhanced caspase-3 activity, and detection of TUNEL-positive cells. Our study demonstrates a single, simple, dependable and green approach for the synthesis of PdNPs using leaf extracts of Evolvulus alsinoides. Furthermore, the in vitro efficacy of PdNPs in human ovarian cancer cells suggests that it could be an effective therapeutic agent for cancer therapy.

  7. Green Chemistry Approach for Synthesis of Effective Anticancer Palladium Nanoparticles.

    Science.gov (United States)

    Gurunathan, Sangiliyandi; Kim, EunSu; Han, Jae Woong; Park, Jung Hyun; Kim, Jin-Hoi

    2015-01-01

    The purpose of this study was to design and synthesize Palladium nanoparticles (PdNPs) using an environmentally friendly approach and evaluate the in vitro efficacy of PdNPs in human ovarian cancer A2780 cells. Ultraviolet-Visible (UV-Vis) spectroscopy was used to monitor the conversion of Pd(II) ions to Pd(0)NPs. X-ray diffraction (XRD) revealed the crystallinity of the as-synthesized PdNPs and Fourier transform infrared spectroscopy (FTIR) further confirmed the role of the leaf extract of Evolvulus alsinoides as a reducing and stabilizing agent for the synthesis of PdNPs. Dynamic light scattering (DLS) and transmission electron microscopy (TEM) showed that the average size of the NPs was 5 nm. After a 24-h exposure to PdNPs, cell viability and light microscopy assays revealed the dose-dependent toxicity of the PdNPs. Furthermore, the dose-dependent cytotoxicity of the PdNPs was confirmed by lactate dehydrogenase (LDH), increased reactive oxygen species (ROS) generation, activation of PdNPs-induced autophagy, impairment of mitochondrial membrane potential (MMP), enhanced caspase-3 activity, and detection of TUNEL-positive cells. Our study demonstrates a single, simple, dependable and green approach for the synthesis of PdNPs using leaf extracts of Evolvulus alsinoides. Furthermore, the in vitro efficacy of PdNPs in human ovarian cancer cells suggests that it could be an effective therapeutic agent for cancer therapy. PMID:26694334

  8. MnO2-induced synthesis of fluorescent polydopamine nanoparticles for reduced glutathione sensing in human whole blood.

    Science.gov (United States)

    Kong, Xiang-Juan; Wu, Shuang; Chen, Ting-Ting; Yu, Ru-Qin; Chu, Xia

    2016-08-25

    Polydopamine (PDA) nanoparticles, as a kind of popular polymer material, have attracted a great deal of attention from various areas including materials science, biomedicine, energy, environmental science and so on owing to their striking physicochemical properties. Herein, we reported for the first time the synthesis of intrinsic fluorescent PDA nanoparticles using MnO2 as an oxidant. In the presence of MnO2, dopamine was quickly oxidized into its quinone derivative, and autopolymerized into fluorescent PDA nanoparticles. Using fluorescent PDA nanoparticles as a fluorescence signal indicator, we further established a cost-effective sensor for rapid, sensitive and selective sensing of reduced glutathione (GSH) based on the redox reaction between MnO2 and GSH, and the key role of MnO2 in the formation of fluorescent PDA nanoparticles. GSH has the capability of reducing MnO2 into Mn(2+), which inhibited the formation of the fluorescent PDA nanoparticles. Thus, the concentration of GSH was directly related to the decreased fluorescence signal intensity of the PDA nanoparticles. The sensor showed good sensing performance for GSH detection with high sensitivity and desirable selectivity over other potential interfering species. Additionally, the sensor exhibited excellent practical applications for GSH detection in human whole blood samples, which presents potential applications in biological detection and clinical diagnosis. PMID:27511888

  9. Design and synthesis of mixed oxides nanoparticles for biofuel applications

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Senniang [Iowa State Univ., Ames, IA (United States)

    2010-05-15

    The work in this dissertation presents the synthesis of two mixed metal oxides for biofuel applications and NMR characterization of silica materials. In the chapter 2, high catalytic efficiency of calcium silicate is synthesized for transesterfication of soybean oil to biodisels. Chapter 3 describes the synthesis of a new Rh based catalyst on mesoporous manganese oxides. The new catalyst is found to have higher activity and selectivity towards ethanol. Chapter 4 demonstrates the applications of solid-state Si NMR in the silica materials.

  10. Recent advances in synthesis and surface modification of superparamagnetic iron oxide nanoparticles with silica

    Science.gov (United States)

    Sodipo, Bashiru Kayode; Aziz, Azlan Abdul

    2016-10-01

    Research on synthesis of superparamagnetic iron oxide nanoparticles (SPION) and its surface modification for biomedical applications is of intense interest. Due to superparamagnetic property of SPION, the nanoparticles have large magnetic susceptibility, single magnetic domain and controllable magnetic behaviour. However, owing to easy agglomeration of SPION, surface modification of the magnetic particles with biocompatible materials such as silica nanoparticle has gained much attention in the last decade. In this review, we present recent advances in synthesis of SPION and various routes of producing silica coated SPION.

  11. Green Synthesis of Gold nanoparticles with Starch-glucose and Application in Bioelectrochemistry

    DEFF Research Database (Denmark)

    Engelbrekt, Christian; Sørensen, Karsten Holm; Zhang, Jingdong;

    2009-01-01

    A method for gold nanoparticle (AuNP) synthesis from buffered glucose and starch solution has been developed and the particles investigated by UV-Vis spectroscopy, transmission electron microscopy (TEM), atomic force microscopy (AFM) and electrochemistry. The synthesis proceeds smoothly in neutra...

  12. Synthesis of monodisperse silver nanoparticles and their self-assembly through simple thermal decomposition approach

    International Nuclear Information System (INIS)

    An easy one phase synthesis of monodisperse silver nanoparticles and their self-assembly has been reported. Thermal decomposition of silver acetate in diphenyl ether in the presence of oleic acid (cis-9-octadecenoic acid) and oleylamine (cis-9-octadecenoic amine) leads to the formation of silver nanoparticles. The amount of organic content present on the surface of Ag nanoparticles affects the self-assembly of nanoparticles. In the presence of oleic acid alone, no self-assembly was observed but the presence of oleyl amine along with oleic acid led to increased organic coating on the surface of silver nanoparticles resulting in the self-assembly (cubic or hexagonal) of monodisperse silver nanoparticles. The silver nanoparticles were characterized by powder X-ray diffraction (XRD), infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), CHN analysis, transmission electron microscopy (TEM), selected area electron diffraction (SAED) and UV-visible spectroscopy.

  13. Controlled Synthesis of Carbon Nanoparticles in a Supercritical Carbon Disulfide System

    Directory of Open Access Journals (Sweden)

    Zhengsong Lou

    2013-12-01

    Full Text Available Carbon nanoparticles with large surface areas were produced by the reduction of carbon disulfide with metallic lithium at 500 °C. The carbon nanoparticles account for about 80% of the carbon product. The carbon nanoparticles were characterized by X-ray powder diffraction, field emission scanning electron microscopy, transmission electron microscopy, high resolution transmission electron microscopy and N2 physisorption. The results showed that carbon nanoparticles predominate in the product. The influence of experimental conditions was investigated, which indicated that temperature plays a crucial role in the formation of carbon nanoparticles. The possible formation mechanism of the carbon nanoparticles was discussed. This method provides a simple and efficient route to the synthesis of carbon nanoparticles.

  14. Synthesis of nanoparticles with frog foam nest proteins

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Hyo-Jick, E-mail: choihc@ucmail.uc.edu; Ebersbacher, Charles F. [University of Cincinnati, School of Energy, Environmental, Biological and Medical Engineering (United States); Myung, Nosang V. [University of California, Riverside, Department of Chemical and Environmental Engineering (United States); Montemagno, Carlo D., E-mail: montemcd@ucmail.uc.edu [University of Cincinnati, School of Energy, Environmental, Biological and Medical Engineering (United States)

    2012-09-15

    Microemulsions provide an efficient means of synthesizing monodispersed nanoparticles. Recent studies have demonstrated potential problems of surfactant due to the interaction with nanoparticles/precursors. To solve the problems, various types of chemical surfactants have been tested, but natural biosurfactants have not received a great deal of attention in engineering application. Here, we report the formation of microemulsions using frog foam nest protein, ranaspumin-2 (RSN-2), based on the hypothesis that RSN-2 assembles at the water-oil interface as a result of conformational change into an extended form. Fluorescence spectroscopic studies showed that RSN-2 undergoes a reversible transition between extended and globular conformation in foams/microemulsions and aqueous solution, respectively. Microemulsions were formulated with RSN-2 to synthesize 8-10 nm superparamagnetic iron oxide nanoparticles by mixing precursor-containing microemulsions with base-containing microemulsions. RSN-2 proteins were recovered from microemulsions and found to be recycled to make foams and microemulsions. Fluorescence spectroscopic analyses showed that RSN-2 maintained its mechanical agitation-induced amphiphilicity throughout multiple foaming/defoaming processes. These results suggest that conformational flexibility and structural stability of RSN-2 in aggressive environments enable the recycled use of RSN-2, elucidating the cost-effective advantage.

  15. Synthesis of magnetic composite nanoparticles enveloped in copolymers specified for scale inhibition application

    Science.gov (United States)

    Do, Bao Phuong Huu; Dung Nguyen, Ba; Duy Nguyen, Hoang; Nguyen, Phuong Tung

    2013-12-01

    We report the synthesis of magnetic iron oxide nanoparticles encapsulated in maleic acid-2-acrylamido-2-methyl-1-propanesulfonate based polymer. This composite nanoparticle is specified for the high-pressure/high-temperature (HPHT) oilfield scale inhibition application. The process includes a facile-ultrasound-supported addition reaction to obtain iron oxide nanoparticles with surface coated by oleic acid. Then via inverse microemulsion polymerization with selected monomers, the specifically designed copolymers have been formatted in nanoscale. The structure and morphology of obtained materials were characterized by transmission electron microscopy (TEM), x-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and the thermal stability. The effectiveness of synthesized compounds as a carbonate scale inhibitor was investigated by testing method NACE standard TM 03-074-95 at aging temperature of 70, 90 and 120 °C. The magnetic nanocomposite particles can be easily collected and detected demonstrating their superior monitoring ability, which is absent in the case of conventional copolymer-based scale inhibitor.

  16. Latex-mediated synthesis of ZnS nanoparticles: green synthesis approach

    Energy Technology Data Exchange (ETDEWEB)

    Hudlikar, Manish; Joglekar, Shreeram [University of Pune, Division of Biochemistry, Department of Chemistry (India); Dhaygude, Mayur [National Chemical Laboratory, Polymer Science and Engineering Division (India); Kodam, Kisan, E-mail: kodam@chem.unipune.ac.in [University of Pune, Division of Biochemistry, Department of Chemistry (India)

    2012-05-15

    A low-cost, green synthesis of ZnS nanoparticles is reported using 0.3 % latex solution prepared from Jatropha curcas L. ZnS nanoparticles were characterized by X-ray diffraction, selected area electron diffraction, transmission electron microscopy, energy dispersive analysis of X-rays, UV-vis optical absorption and photoluminescence techniques. Fourier Transform Infrared Spectroscopy was performed to find the role of cyclic peptides namely curcacycline A (an octapeptide), curcacycline B (a nonapeptide) and curcain (an enzyme) as a possible reducing and stabilizing agents present in the latex of J. curcas L. The average size of ZnS nanoparticles was found to be 10 nm. Latex of J. curcas L. itself acts as a source of sulphide (S{sup -2}) ions that are donated to Zn ions under present experimental conditions. Source of sulphide (S{sup -2}) ions is still unclear, but we speculate that cysteine or thiol residues present in enzyme curcain may be donating these sulphide (S{sup -2}) ions.

  17. Magnetic nanoparticle-based cancer nanodiagnostics

    Institute of Scientific and Technical Information of China (English)

    Muhammad Zubair Yousaf; Yu Jing; Hou Yang-Long; Gao Song

    2013-01-01

    Diagnosis facilitates the discovery of an impending disease.A complete and accurate treatment of cancer depends heavily on its early medical diagnosis.Cancer,one of the most fatal diseases world-wide,consistently affects a larger number of patients each year.Magnetism,a physical property arising from the motion of electrical charges,which causes attraction and repulsion between objects and does not involve radiation,has been under intense investigation for several years.Magnetic materials show great promise in the application of image contrast enhancement to accurately image and diagnose cancer.Chelating gadolinium (Gd Ⅲ) and magnetic nanoparticles (MNPs) have the prospect to pave the way for diagnosis,operative management,and adjuvant therapy of different kinds of cancers.The potential of MNP-based magnetic resonance (MR) contrast agents (CAs) now makes it possible to image portions of a tumor in parts of the body that would be unclear with the conventional magnetic resonance imaging (MRI).Multiple functionalities like variety of targeting ligands and image contrast enhancement have recently been added to the MNPs.Keeping aside the additional complexities in synthetic steps,costs,more convoluted behavior,and effects in-vivo,multifunctional MNPs still face great regulatory hurdles before clinical availability for cancer patients.The trade-off between additional functionality and complexity is a subject of ongoing debate.The recent progress regarding the types,design,synthesis,morphology,characterization,modification,and the in-vivo and in-vitro uses of different MRI contrast agents,including MNPs,to diagnose cancer will be the focus of this review.As our knowledge of MNPs' characteristics and applications expands,their role in the future management of cancer patients will become very important.Current hurdles are also discussed,along with future prospects of MNPs as the savior of cancer victims.

  18. Magnetic nanoparticle-based cancer nanodiagnostics

    Science.gov (United States)

    Zubair, Yousaf Muhammad; Yu, Jing; Hou, Yang-Long; Gao, Song

    2013-05-01

    Diagnosis facilitates the discovery of an impending disease. A complete and accurate treatment of cancer depends heavily on its early medical diagnosis. Cancer, one of the most fatal diseases world-wide, consistently affects a larger number of patients each year. Magnetism, a physical property arising from the motion of electrical charges, which causes attraction and repulsion between objects and does not involve radiation, has been under intense investigation for several years. Magnetic materials show great promise in the application of image contrast enhancement to accurately image and diagnose cancer. Chelating gadolinium (Gd III) and magnetic nanoparticles (MNPs) have the prospect to pave the way for diagnosis, operative management, and adjuvant therapy of different kinds of cancers. The potential of MNP-based magnetic resonance (MR) contrast agents (CAs) now makes it possible to image portions of a tumor in parts of the body that would be unclear with the conventional magnetic resonance imaging (MRI). Multiple functionalities like variety of targeting ligands and image contrast enhancement have recently been added to the MNPs. Keeping aside the additional complexities in synthetic steps, costs, more convoluted behavior, and effects in-vivo, multifunctional MNPs still face great regulatory hurdles before clinical availability for cancer patients. The trade-off between additional functionality and complexity is a subject of ongoing debate. The recent progress regarding the types, design, synthesis, morphology, characterization, modification, and the in-vivo and in-vitro uses of different MRI contrast agents, including MNPs, to diagnose cancer will be the focus of this review. As our knowledge of MNPs' characteristics and applications expands, their role in the future management of cancer patients will become very important. Current hurdles are also discussed, along with future prospects of MNPs as the savior of cancer victims.

  19. Aloe barbadensis Miller mediated green synthesis of mono-disperse copper oxide nanoparticles: Optical properties

    Science.gov (United States)

    Gunalan, Sangeetha; Sivaraj, Rajeshwari; Venckatesh, Rajendran

    2012-11-01

    In this paper, we report on the synthesis of nanostructured copper oxide particles by both chemical and biological method. A facile and efficient synthesis of copper oxide nanoparticles was carried out with controlled surface properties via green chemistry approach. The CuO nanoparticles synthesized are monodisperse and versatile and were characterized with the help of UV-Vis, PL, FT-IR, XRD, SEM, and TEM techniques. The particles are crystalline in nature and average sizes were between 15 and 30 nm. The morphology of the nanoparticles can be controlled by tuning the amount of Aloe vera extract. This new eco-friendly approach of synthesis is a novel, cheap, and convenient technique suitable for large scale commercial production and health related applications of CuO nanoparticles.

  20. Radio frequency radiation-induced hyperthermia using Si nanoparticle-based sensitizers for mild cancer therapy

    Science.gov (United States)

    Tamarov, Konstantin P.; Osminkina, Liubov A.; Zinovyev, Sergey V.; Maximova, Ksenia A.; Kargina, Julia V.; Gongalsky, Maxim B.; Ryabchikov, Yury; Al-Kattan, Ahmed; Sviridov, Andrey P.; Sentis, Marc; Ivanov, Andrey V.; Nikiforov, Vladimir N.; Kabashin, Andrei V.; Timoshenko, Victor Yu

    2014-11-01

    Offering mild, non-invasive and deep cancer therapy modality, radio frequency (RF) radiation-induced hyperthermia lacks for efficient biodegradable RF sensitizers to selectively target cancer cells and thus avoid side effects. Here, we assess crystalline silicon (Si) based nanomaterials as sensitizers for the RF-induced therapy. Using nanoparticles produced by mechanical grinding of porous silicon and ultraclean laser-ablative synthesis, we report efficient RF-induced heating of aqueous suspensions of the nanoparticles to temperatures above 45-50°C under relatively low nanoparticle concentrations (nanoparticles the heating rate was linearly dependent on nanoparticle concentration, while laser-ablated nanoparticles demonstrated a remarkably higher heating rate than porous silicon-based ones for the whole range of the used concentrations from 0.01 to 0.4 mg/mL. The observed effect is explained by the Joule heating due to the generation of electrical currents at the nanoparticle/water interface. Profiting from the nanoparticle-based hyperthermia, we demonstrate an efficient treatment of Lewis lung carcinoma in vivo. Combined with the possibility of involvement of parallel imaging and treatment channels based on unique optical properties of Si-based nanomaterials, the proposed method promises a new landmark in the development of new modalities for mild cancer therapy.

  1. Nanoparticles with entrapped α-tocopherol: synthesis, characterization, and controlled release

    Science.gov (United States)

    Zigoneanu, Imola Gabriela; Astete, Carlos Ernesto; Mirela Sabliov, Cristina

    2008-03-01

    An emulsion evaporation method was used to synthesize spherical poly(DL-lactide-co-glycolide) (PLGA) nanoparticles with entrapped α-tocopherol. Two different surfactants were used: sodium dodecyl sulfate (SDS) and poly(vinyl alcohol) (PVA). For SDS nanoparticles, the size of the nanoparticles decreased significantly with the entrapment of α-tocopherol in the PLGA matrix, while the size of PVA nanoparticles remained unchanged. The polydispersity index after synthesis was under 0.100 for PVA nanoparticles and around 0.150 for SDS nanoparticles. The zeta potential was negative for all PVA nanoparticles. The entrapment efficiency of α-tocopherol in the polymeric matrix was approximately 89% and 95% for nanoparticles with 8% and 16% α-tocopherol theoretical loading, respectively. The residual PVA associated with the nanoparticles after purification was approximately 6% ( w/w relative to the nanoparticles). The release profile showed an initial burst followed by a slower release of the α-tocopherol entrapped inside the PLGA matrix. The release for nanoparticles with 8% α-tocopherol theoretical loading (86% released in the first hour) was faster than the release for the nanoparticles with 16% α-tocopherol theoretical loading (34% released in the first hour).

  2. Aqueous starch as a stabilizer in zinc oxide nanoparticle synthesis via laser ablation

    International Nuclear Information System (INIS)

    Highlights: ► Zinc oxide nanoparticles were synthesized via LASiS in aqueous starch solution. ► Nanoparticles of ±15 nm are produced with a narrow size distribution. ► Starch can be used as a template to control nanoparticle size. ► Starch stabilizes zinc oxide nanoparticles in solution through steric hindrance. - Abstract: Zinc oxide is a semiconductor with exceptional thermal, luminescent and electrical properties, even compared with other semiconducting nanoparticles. Its potential for advanced applications in lasers and light emitting diodes, as bio-imaging agent, in biosensors and as drug delivery vehicles, in ointments, coatings and pigments has pulled zinc oxide into the focus of various scientific and engineering research fields. Recently we started investigating if nanoparticle synthesis via laser ablation in the presence of natural stabilizers allows control over size and shape and constitutes a useful, uncomplicated alternative over conventional synthesis methods. In the current paper, we determined the ability of natural starch to act as a size controller and stabilizer in the preparation of zinc oxide nanoparticles via ablation of a ZnO plate in a starch solution with a nanosecond Q-Switched Nd:YAG pulsed laser at its original wavelength (λ = 1064 nm). Our results show that the particle diameter decreases with increasing laser irradiation time to a mean nanoparticle size of approximately 15 nm with a narrow size distribution. Furthermore, the obtained particle size in starch solution is considerably smaller compared with analogous ZnO nanoparticle synthesis in distilled water. The synthesized and capped nanoparticles retained their photoluminescent properties, but showed blue emission rather than the often reported green luminescence. Evaluation of old preparations compared with freshly made samples showed no agglomeration or flocculation, which was reflected in no significant change in the ZnO nanoparticle size and size distribution. Overall

  3. Synthesis of TiO{sub 2} rutile nanoparticles by PLA in solution

    Energy Technology Data Exchange (ETDEWEB)

    Caratto, V., E-mail: caratto@chimica.unige.it [Dipartimento di Chimica e Chimica Industriale, Universita di Genova, Via Dodecaneso 31, 16146 Genova (Italy); CNR-SPIN, Corso Perrone 24, 16152 Genova (Italy); Ferretti, M.; Setti, L. [Dipartimento di Chimica e Chimica Industriale, Universita di Genova, Via Dodecaneso 31, 16146 Genova (Italy); CNR-SPIN, Corso Perrone 24, 16152 Genova (Italy)

    2012-01-15

    This paper describes the synthesis of TiO{sub 2} nanoparticles by laser ablation in solution synthesis (Lasis). The laser excimer beam passes through a focusing lens and it is sent to the reaction chamber. The frequency used during the synthesis was 20 Hz, intensity 26 kV The metal ablated by the laser beam undergoes an oxidation process resulting from the reaction with water. We obtain TiO{sub 2} nanoparticles with average size of 6.5 nm, crystallized in the rutile structure. The crystallographic and morphological structure was studied by transmission electron microscopy.

  4. Synthesis and characterization of core-shell structure silica-coated Fe29.5Ni70.5 nanoparticles

    OpenAIRE

    Ammar, M; Mazaleyrat, F.; Bonnet, J.P.; Audebert, P.; Brosseau, A; Wang, G.; Champion, Y

    2007-01-01

    In view of potential applications of magnetic particles in biomedicine and electromagnetic devices, we made use of the classical Stober method base-catalysed hydrolysis and condensation of tetraethoxysilane (TEOS) to encapsulate FeNi nanoparticles within a silica shell. An original stirring system under high power ultrasounds made possible to disperse the otherwise agglomerated particles. Sonication guaranteed particles to remain dispersed during the Stober synthesis and also improved the eff...

  5. One-pot green synthesis of biocompatible arginine-stabilized magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Wang Zhongjun; Zhu Hui; Wang Xiaolei; Yang Fan; Yang Xiurong, E-mail: xryang@ciac.jl.c [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022 (China)

    2009-11-18

    A green one-step approach has been developed for the synthesis of amino-functionalized magnetite nanoparticles. The synthesis was accomplished by simply mixing FeCl{sub 2} with arginine under ambient conditions. It was found that the Fe{sup 2+}/arginine molar ratio, reaction duration and temperature greatly influence the size, morphology and composition of magnetic nanoparticles. The arginine-stabilized magnetic nanoparticles were characterized by transmission electron microscopy, x-ray diffraction, x-ray photoelectron spectroscopy, thermogravimetric analysis, and Fourier transform infrared spectroscopy techniques. The results show that the prepared nanoparticles are spherically shaped with a nearly uniform size distribution and pure magnetite phase. The presence of arginine on the magnetic nanoparticle surface has been confirmed and the amount of surface arginine varies with the Fe{sup 2+}/arginine molar ratio. The surface amine densities are calculated to be 5.60 and 7.84 {mu}mol mg{sup -1} for magnetic nanoparticles prepared at 1:1 and 1:2 Fe{sup 2+}/arginine molar ratio, respectively. The as-synthesized nanoparticles show superparamagnetic behavior at room temperature and good solubility in water. In addition, using a similar synthesis procedure, we have been able to synthesize superparamagnetic manganese and cobalt ferrite nanoparticles.

  6. One-pot green synthesis of biocompatible arginine-stabilized magnetic nanoparticles

    International Nuclear Information System (INIS)

    A green one-step approach has been developed for the synthesis of amino-functionalized magnetite nanoparticles. The synthesis was accomplished by simply mixing FeCl2 with arginine under ambient conditions. It was found that the Fe2+/arginine molar ratio, reaction duration and temperature greatly influence the size, morphology and composition of magnetic nanoparticles. The arginine-stabilized magnetic nanoparticles were characterized by transmission electron microscopy, x-ray diffraction, x-ray photoelectron spectroscopy, thermogravimetric analysis, and Fourier transform infrared spectroscopy techniques. The results show that the prepared nanoparticles are spherically shaped with a nearly uniform size distribution and pure magnetite phase. The presence of arginine on the magnetic nanoparticle surface has been confirmed and the amount of surface arginine varies with the Fe2+/arginine molar ratio. The surface amine densities are calculated to be 5.60 and 7.84 μmol mg-1 for magnetic nanoparticles prepared at 1:1 and 1:2 Fe2+/arginine molar ratio, respectively. The as-synthesized nanoparticles show superparamagnetic behavior at room temperature and good solubility in water. In addition, using a similar synthesis procedure, we have been able to synthesize superparamagnetic manganese and cobalt ferrite nanoparticles.

  7. Antibacterial Activity of Green Synthesis of Iron Nanoparticles Using Lawsonia inermis and Gardenia jasminoides Leaves Extract

    Directory of Open Access Journals (Sweden)

    Tayyaba Naseem

    2015-01-01

    Full Text Available Recently, development of reliable experimental protocols for synthesis of metal nanoparticles with desired morphologies and sizes has become a major focus of researchers. Green synthesis of metallic nanoparticles has accumulated an ultimate interest over the last decade due to their distinctive properties that make them applicable in various fields of science and technology. Metal nanoparticles that are synthesized by using plants have emerged as nontoxic and ecofriendly. In this study a very cheap and simple conventional heating method was used to obtain the iron nanoparticles (FeNPs using the leaves extract of Lawsonia inermis and Gardenia jasminoides plant. The iron nanoparticles were characterized by thermal gravimetric analysis (TGA, Fourier transform infrared spectroscopy (FT-IR, transmission electron microscopy (TEM, scanning electron microscopy (SEM, atomic force microscopy (AFM, and X-ray diffraction (XRD. The antibacterial activity was studied against Escherichia coli, Salmonella enterica, Proteus mirabilis, and Staphylococcus aureus by using well-diffusion method.

  8. Algae mediated synthesis of cadmium sulphide nanoparticles and their application in bioremediation

    Science.gov (United States)

    Prasad Mandal, Ranju; Sekh, Sanoyaz; Sarkar, Neera Sen; Chattopadhyay, Dipankar; De, Swati

    2016-05-01

    The present work is a study on the biological synthesis of cadmium sulphide (CdS) nanoparticles using blue-green algae that is popularly used as a food supplement. This synthesis is unique in the sense that no external sulphur precursor is required, the CdS nanoparticles are synthesized in situ in the algal medium. The CdS nanoparticles thus synthesized are photoluminescent and can act as highly efficient photocatalysts for degradation of the dye pollutant malachite green. Thus the CdS nanoparticles synthesized in situ in the algae conform to the desired criteria of waste water treatment i.e. biosorption of the pollutant and its subsequent degradation. The novelty of this work also lies in its potential for use in bioremediation by conversion of the toxic Cd(II) ion to less toxic CdS nanoparticles within the algal framework.

  9. High-Energy-Low-Temperature Technologies for the Synthesis of Nanoparticles: Microwaves and High Pressure

    Directory of Open Access Journals (Sweden)

    Witold Lojkowski

    2014-11-01

    Full Text Available Microwave Solvothermal Synthesis (MSS is a chemical technology, where apart from possible effects of microwaves on the chemical reaction paths, microwave heating allows the precise planning of a time-temperature schedule, as well as to achieve high super-saturation of the reagents uniformly in the reactor vessel. Thus, MSS is suitable for production of nanoparticles with small grain size distribution and a high degree of crystallinity. A further advantage of the technology is a much lower synthesis temperature than for gas phase, plasma or sol-gel technologies. New reactors have been developed to exploit these advantages of the MSS technology of nanoparticles synthesis and to scale up the production rate. Reactor design and realization has been shown to be decisive and critical for the control of the MSS technology. Examples of oxidic and phosphatic nanoparticles synthesis have been reported.

  10. Preparation of bicontinuous mesoporous silica and organosilica materials containing gold nanoparticles by co-synthesis method

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Byunghwan [Korea Institute of Industrial Technology, ChonAn, Korea; Zhu, Haoguo [ORNL; Zhang, Zongtao [ORNL; Overbury, Steven {Steve} H [ORNL; Dai, Sheng [ORNL

    2004-01-01

    Catalytic activities of gold strongly depend on its particle size. It is necessary to have homogeneous distributions of small gold nanoparticles with diameters between 2 and 5 nm for excellent catalytic activities. In this study, gold-containing mesoporous silica materials were prepared by a co-synthesis method. The essence of this sol-gel co-synthesis method is to combine together neutral surfactant template synthesis of mesoporous silica materials with the introduction of metal ions via bifunctional silane ligands, so that the formation of mesostructures and metal-ion doping occur simultaneously. The formation of gold nanoparticles with size less than 5 nm inside mesoporous materials (HMS, MSU, and PMO) has been achieved by this co-synthesis sol-gel process. In addition, the effects of post-treatments, such as calcination and reduction, on pore structures and nanoparticle size distributions were also investigated.

  11. Ultrasmall dual-modality silica nanoparticle drug conjugates: Design, synthesis, and characterization.

    Science.gov (United States)

    Yoo, Barney; Ma, Kai; Zhang, Li; Burns, Andrew; Sequeira, Sonia; Mellinghoff, Ingo; Brennan, Cameron; Wiesner, Ulrich; Bradbury, Michelle S

    2015-11-15

    The physicochemical design and synthesis of effective cancer-directed and particle-based nanotherapeutic imaging agents remains a challenging task. Of critical importance is the ability to demonstrate maximum delivery, retention, and treatment efficacy for platforms designed to deposit their cargo at sites of disease without attendant dose-limiting toxicity. In this work, we describe dual-modality nanoparticle drug conjugates (NDCs) which utilize protease sensitive linkers to attached drug compounds and imaging labels to a clinically translated class of ultrasmall silica nanoparticle (C' dots). We describe the synthesis and characterization of these linker-drug constructs. Linkers incorporating dipeptide enzyme substrates are attached to analogs of a prototypical epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI), through a cleavable amide bond or para-aminobenzyloxycarbonyl (PABC) group. These constructs are conjugated onto C' dots leading to the desired NDCs. These NDCs exhibit fast and predictable release kinetics in the presence of model proteases, and are stable in various biological media. Finally, in vitro assays show NDCs to be highly active in reducing phosphorylated EGFR levels in H1650 cells, a human tumor-derived cell line. The data suggests that NDCs exhibit desirable properties that warrant further development toward oncological therapy. PMID:26462054

  12. Synthesis, characterization and fabrication of copper nanoparticles in N-isopropylacrylamide based co-polymer microgels for degradation of p-nitrophenol

    Directory of Open Access Journals (Sweden)

    Farooqi Zahoor H.

    2015-03-01

    Full Text Available Poly(N-isopropylacrylamide-co-acrylic acid [P(NIPAM-co-AAc] microgels were synthesized by precipitation polymerization. Copper nanoparticles were successfully fabricated inside the microgels by in-situ reduction of copper ions in an aqueous medium. The microgels were characterized by Fourier Transform Infrared Spectroscopy (FT-IR and Dynamic Light Scattering (DLS. Hydrodynamic radius of P(NIPAM-co-AAc microgel particles increased with an increase in pH in aqueous medium at 25 °C. Copper-poly(N-isopropylacrylamide-co-acrylic acid [Cu-P(NIPAM-co-AAc] hybrid microgels were used as a catalyst for the reduction of 4-nitrophenol (4-NP. Effect of temperature, concentration of sodium borohydride (NaBH4 and catalyst dosage on the value of apparent rate constant (kapp for catalytic reduction of 4-NP in the presence of Cu-P(NIPAM-co-AAc hybrid microgels were investigated by UV-Vis spectrophotometry. It was found that the value of kapp for catalytic reduction of 4-NP in the presence of Cu-P(NIPAM-co-AAc hybrid microgel catalyst increased with an increase in catalyst dosage, temperature and concentration of NaBH4 in aqueous medium. The results were discussed in terms of diffusion of reactants towards catalyst surface and swelling-deswelling of hybrid microgels.

  13. Synthesis and characterization of a Noble metal Enhanced Optical Nanohybrid (NEON): a high brightness detection platform based on a dye-doped silica nanoparticle.

    Science.gov (United States)

    Roy, Shibsekhar; Dixit, Chandra K; Woolley, Robert; O'Kennedy, Richard; McDonagh, Colette

    2012-05-29

    A highly bright and photostable, fluorescent nanohybrid particle is presented which consists of gold nanoparticles (GNPs) embedded in dye-doped silica in a core-shell configuration. The dye used is the near-infrared emitting 4,5-benzo-5'-(iodoacetaminomethyl)-1',3,3,3',3'-pentamethyl-1-(4-sulfobutyl) indodicarbo cyanine. The nanohybrid architecture comprises a GNP core which is separated from a layer of dye molecules by a 15 nm buffer layer and has an outer protective, undoped silica shell. Using this architecture, a brightness factor of 550 has been achieved compared to the free dye. This hybrid system, referred to as Noble metal Enhanced Optical Nanohybrid (NEON) in this paper, is the first nanohybrid construct to our knowledge which demonstrates such tunable fluorescence property. NEON has enhanced photostability compared to the free dye and compared to a control particle without GNPs. Furthermore, the NEON particle, when used as a fluorescent label in a model bioassay, shows improved performance over assays using a conventional single dye molecule label.

  14. Click chemistry-based synthesis of water-dispersible hydrophobic magnetic nanoparticles for use in solid phase extraction of non-steroidal anti-inflammatory drugs

    International Nuclear Information System (INIS)

    Magnetic nanoparticles (MNPs), prepared via thiol-ene click chemistry and containing both diol and octadecyl groups, are shown to possess both hydrophobic and hydrophilic functionalities. They display excellent dispersibility in water and also are capable of extracting non-steroidal anti-inflammatory drugs (NSAIDs) from water samples. The MNPs can be magnetically separated, and the NSAIDs eluted with acetonitrile-water (9:1, v:v) and submitted to high performance liquid chromatographic analysis. Extraction variables, such as the kind of ion-pairing reagents, amount of MNPs, pH of sample solution, extraction and desorption time, volume of desorption solvent and salt addition, were optimized. Under optimum conditions, the method has a wide analytical range (from 5 to 800 ng∙mL-1), good reproducibility with intra-day and inter-day relative standard deviations of <19.2 % (for n = 6), and low detection limits of 0.32 to 1.44 ng∙mL-1 for water samples. The results demonstrate that the material possesses good water compatibility, thus warranting ease of operation and good reproducibility. (author)

  15. Solvothermal synthesis and characterization of monodisperse superparamagnetic iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Li, Shichuan; Zhang, Tonglai; Tang, Runze; Qiu, Hao [State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081 (China); Wang, Caiqin [Shandong Special Industry Group Co., Ltd, Shandong 255201 (China); Zhou, Zunning [State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081 (China)

    2015-04-01

    A series of magnetic iron oxide nanoparticle clusters with different structure guide agents were synthesized by a modified solvothermal method and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), thermogravimetric analyses (TG), a vibrating sample magnetometer (VSM) and Fourier transform infrared spectroscopy (FTIR). It is found that the superparamagnetic nanoparticles guided by NaCit (sodium citrate) have high saturation magnetization (M{sub s}) of 69.641 emu/g and low retentivity (M{sub r}) of 0.8 emu/g. Guiding to form superparamagnetic clusters with size range of 80–110 nm, the adherent small-molecule citrate groups on the surface prevent the prefabricated ferrite crystals growing further. In contrast, the primary small crystal guided and stabilized by the PVP long-chain molecules assemble freely to larger ones and stop growing in size range of 100–150 nm, which has saturation magnetization (M{sub s}) of 97.979 emu/g and retentivity (M{sub r}) of 46.323 emu/g. The relevant formation mechanisms of the two types of samples are proposed at the end. The superparamagnetic ferrite clusters guided by sodium citrate are expected to be used for movement controlling of passive interference particles to avoid aggregation and the sample guided by PVP will be a candidate of nanometer wave absorbing material. - Highlights: • A facile synthesis of two kinds of monodisperse iron oxide nano-particle clusters was performed via a modified one-step solvothermal method in this work. • The NaCit and PVP as different guiding agents are used to control the formation and aggregation of nano-crystals during reacting and the ripening processes. • The superparamagnetic NaCit–Fe{sub 3}O{sub 4} samples have high saturation magnetization (M{sub s}) of 69.641 emu/g and low retentivity (M{sub r}) of 0.8 emu/g. • The relevant formation mechanisms of the two types of samples are proposed.

  16. Synthesis of Monodisperse Chitosan Nanoparticles and in Situ Drug Loading Using Active Microreactor.

    Science.gov (United States)

    Kamat, Vivek; Marathe, Ila; Ghormade, Vandana; Bodas, Dhananjay; Paknikar, Kishore

    2015-10-21

    Chitosan nanoparticles are promising drug delivery vehicles. However, the conventional method of unregulated mixing during ionic gelation limits their application because of heterogeneity in size and physicochemical properties. Therefore, a detailed theoretical analysis of conventional and active microreactor models was simulated. This led to design and fabrication of a polydimethylsiloxane microreactor with magnetic micro needles for the synthesis of monodisperse chitosan nanoparticles. Chitosan nanoparticles synthesized conventionally, using 0.5 mg/mL chitosan, were 250 ± 27 nm with +29.8 ± 8 mV charge. Using similar parameters, the microreactor yielded small size particles (154 ± 20 nm) at optimized flow rate of 400 μL/min. Further optimization at 0.4 mg/mL chitosan concentration yielded particles (130 ± 9 nm) with higher charge (+39.8 ± 5 mV). The well-controlled microreactor-based mixing generated highly monodisperse particles with tunable properties including antifungal drug entrapment (80%), release rate, and effective activity (MIC, 1 μg/mL) against Candida. PMID:26448128

  17. Biogenic synthesis of silver nanoparticles by leaf extract of Cassia angustifolia

    Science.gov (United States)

    Amaladhas, T. Peter; Sivagami, S.; Akkini Devi, T.; Ananthi, N.; Priya Velammal, S.

    2012-12-01

    In this study Cassia angustifolia (senna) is used for the environmentally friendly synthesis of silver nanoparticles. Stable silver nanoparticles having symmetric surface plasmon resonance (SPR) band centred at 420 nm were obtained within 10 min at room temperature by treating aqueous solutions of silver nitrate with C. angustifolia leaf extract. The water soluble components from the leaves, probably the sennosides, served as both reducing and capping agents in the synthesis of silver nanoparticles. The nanoparticles were characterized using UV-Vis, Fourier transform infrared (FTIR) spectroscopic techniques and transmission electron microscopy (TEM). The nanoparticles were poly-dispersed, spherical in shape with particle size in the range 9-31 nm, the average size was found to be 21.6 nm at pH 11. The zeta potential was -36.4 mV and the particles were stable for 6 months. The crystalline phase of the nanoparticles was confirmed from the selected area diffraction pattern (SAED). The rate of formation and size of silver nanoparticles were pH dependent. Functional groups responsible for capping of silver nanoparticles were identified from the FTIR spectrum. The synthesized silver nanoparticles exhibited good antibacterial potential against Escherichia coli and Staphylococcus aureus.

  18. Microbial synthesis of iron-based nanomaterials—A review

    Indian Academy of Sciences (India)

    Abhilash; K Revati; B D Pandey

    2011-04-01

    Nanoparticles are the materials having dimensions of the order of 100 nm or less. They exhibit a high surface/volume ratio leading to different properties far different from those of the bulk materials. The development of uniform nanoparticles has been intensively pursued because of their technological and fundamental scientific importance. A number of chemical methods are available and are extensively used, but these are often energy intensive and employ toxic chemicals. An alternative approach for the synthesis of uniform nanoparticles is the biological route that occurs at ambient temperature, pressure and at neutral pH. The main aim of this review is to enlist and compare various methods of synthesis of iron-based nanoparticles with emphasis on the biological method. Biologically induced and controlled mineralization mechanisms are the two modes through which the micro-organisms synthesize iron oxide nanoparticles. In biologically induced mineralization (BIM) mode, the environmental factors like pH, pO2, pCO2, redox potential, temperature etc govern the synthesis of iron oxide nanoparticles. In contrast, biologically controlled mineralization (BCM) process initiates the micro-organism itself to control the synthesis. BIM can be observed in the Fe(III) reducing bacterial species of Shewanella, Geobacter, Thermoanaerobacter, and sulphate reducing bacterial species of Archaeoglobus fulgidus, Desulfuromonas acetoxidans, whereas BCM mode can be observed in the magnetotactic bacteria (MTB) like Magnetospirillum magnetotacticum, M. gryphiswaldense and sulphate-reducing magnetic bacteria (Desulfovibrio magneticus). Magnetite crystals formed by Fe(III)-reducing bacteria are epicellular, poorly crystalline, irregular in shapes, having a size range of 10–50 nm super-paramagnetic particles, with a saturation magnetization value ranging from 75–77 emu/g and are not aligned in chains. Magnetite crystals produced by MTB have uniform species-specific morphologies and sizes

  19. Synthesis and characterization of near IR fluorescent albumin nanoparticles for optical detection of colon cancer

    International Nuclear Information System (INIS)

    Near IR (NIR) fluorescent human serum albumin (HSA) nanoparticles hold great promise as contrast agents for tumor diagnosis. HSA nanoparticles are considered to be biocompatible, non-toxic and non-immunogenic. In addition, NIR fluorescence properties of these nanoparticles are important for in vivo tumor diagnostics, with low autofluorescence and relatively deep penetration of NIR irradiation due to low absorption of biomatrices. The present study describes the synthesis of new NIR fluorescent HSA nanoparticles, by entrapment of a NIR fluorescent dye within the HSA nanoparticles, which also significantly increases the photostability of the dye. Tumor-targeting ligands such as peanut agglutinin (PNA) and anti-carcinoembryonic antigen antibodies (anti-CEA) were covalently conjugated to the NIR fluorescent albumin nanoparticles, increasing the potential fluorescent signal in tumors with upregulated corresponding receptors. Specific colon tumor detection by the NIR fluorescent HSA nanoparticles was demonstrated in a chicken embryo model and a rat model. In future work we also plan to encapsulate cancer drugs such as doxorubicin within the NIR fluorescent HSA nanoparticles for both colon cancer imaging and therapy. - Highlights: ► Near IR human serum albumin nanoparticles were synthesized and characterized. ► Nanoparticles were shown to be physically and chemically stable and photostable. ► Tumor-targeting ligands were covalently conjugated to the nanoparticles. ► Specific colon cancer tumor detection was demonstrated in chicken-embryo and rat models.

  20. Synthesis and characterization of near IR fluorescent albumin nanoparticles for optical detection of colon cancer

    Energy Technology Data Exchange (ETDEWEB)

    Cohen, Sarit; Pellach, Michal [Department of Chemistry, Bar-Ilan Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat-Gan 52900 (Israel); Kam, Yossi [Institute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, P.O. Box 12065, Jerusalem 91120 (Israel); Grinberg, Igor; Corem-Salkmon, Enav [Department of Chemistry, Bar-Ilan Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat-Gan 52900 (Israel); Rubinstein, Abraham [Institute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, P.O. Box 12065, Jerusalem 91120 (Israel); Margel, Shlomo, E-mail: shlomo.margel@mail.biu.ac.il [Department of Chemistry, Bar-Ilan Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat-Gan 52900 (Israel)

    2013-03-01

    Near IR (NIR) fluorescent human serum albumin (HSA) nanoparticles hold great promise as contrast agents for tumor diagnosis. HSA nanoparticles are considered to be biocompatible, non-toxic and non-immunogenic. In addition, NIR fluorescence properties of these nanoparticles are important for in vivo tumor diagnostics, with low autofluorescence and relatively deep penetration of NIR irradiation due to low absorption of biomatrices. The present study describes the synthesis of new NIR fluorescent HSA nanoparticles, by entrapment of a NIR fluorescent dye within the HSA nanoparticles, which also significantly increases the photostability of the dye. Tumor-targeting ligands such as peanut agglutinin (PNA) and anti-carcinoembryonic antigen antibodies (anti-CEA) were covalently conjugated to the NIR fluorescent albumin nanoparticles, increasing the potential fluorescent signal in tumors with upregulated corresponding receptors. Specific colon tumor detection by the NIR fluorescent HSA nanoparticles was demonstrated in a chicken embryo model and a rat model. In future work we also plan to encapsulate cancer drugs such as doxorubicin within the NIR fluorescent HSA nanoparticles for both colon cancer imaging and therapy. - Highlights: Black-Right-Pointing-Pointer Near IR human serum albumin nanoparticles were synthesized and characterized. Black-Right-Pointing-Pointer Nanoparticles were shown to be physically and chemically stable and photostable. Black-Right-Pointing-Pointer Tumor-targeting ligands were covalently conjugated to the nanoparticles. Black-Right-Pointing-Pointer Specific colon cancer tumor detection was demonstrated in chicken-embryo and rat models.

  1. Synthesis, characterization, applications, and challenges of iron oxide nanoparticles.

    Science.gov (United States)

    Ali, Attarad; Zafar, Hira; Zia, Muhammad; Ul Haq, Ihsan; Phull, Abdul Rehman; Ali, Joham Sarfraz; Hussain, Altaf

    2016-01-01

    Recently, iron oxide nanoparticles (NPs) have attracted much consideration due to their unique properties, such as superparamagnetism, surface-to-volume ratio, greater surface area, and easy separation methodology. Various physical, chemical, and biological methods have been adopted to synthesize magnetic NPs with suitable surface chemistry. This review summarizes the methods for the preparation of iron oxide NPs, size and morphology control, and magnetic properties with recent bioengineering, commercial, and industrial applications. Iron oxides exhibit great potential in the fields of life sciences such as biomedicine, agriculture, and environment. Nontoxic conduct and biocompatible applications of magnetic NPs can be enriched further by special surface coating with organic or inorganic molecules, including surfactants, drugs, proteins, starches, enzymes, antibodies, nucleotides, nonionic detergents, and polyelectrolytes. Magnetic NPs can also be directed to an organ, tissue, or tumor using an external magnetic field for hyperthermic treatment of patients. Keeping in mind the current interest in iron NPs, this review is designed to report recent information from synthesis to characterization, and applications of iron NPs. PMID:27578966

  2. Synthesis of magnetite nanoparticles-{beta}-cyclodextrin complex

    Energy Technology Data Exchange (ETDEWEB)

    Cobos Cruz, L.A.; Martinez Perez, C.A. [Instituto de Ingenieria y Tecnologia, Universidad Autonoma de Cd. Juarez, Ave. del Charro 450, Col Partido Romero, C.P. 32360, Cd. Juarez Chih. (Mexico); Monreal Romero, H.A. [Facultad de Odontologia, Universidad Autonoma de Chihuahua, Ciudad Universitaria Campus I, C.P. 31000, Chihuahua, Chi. Mexico (Mexico); Garcia Casillas, P.E. [Instituto de Ingenieria y Tecnologia, Universidad Autonoma de Cd. Juarez, Ave. del Charro 450, Col Partido Romero, C.P. 32360, Cd. Juarez Chih. (Mexico)], E-mail: pegarcia@uacj.mx

    2008-10-20

    In this work, the synthesis and characterization of a magnetite (M) and {beta}-cyclodextrin (CD) complex is presented. The chemical bonding between the magnetite and CD was studied as evidence of host-guest interaction; therefore the CD works like a reactor with the magnetite inside of it, as consequence the growth of the particle is restricted by the electrostatic interaction of M-CD complex. The particle size of the magnetite-cyclodextrin complex (M-CD) decreased 79.1% with 0.5% of CD. The average particle size of the M-CD complex was 10 nm. The saturation magnetization ({sigma}{sub s}) and intrinsic coercivity (H{sub c}) increased 10% and 20%, respectively. In order to understand how the the CD affects the results obtained, the second derivate of remission function was obtained from the ultraviolet-visible spectra (UV-vis). Fourier transform infrared spectroscopy (FTIR) was used to elucidate the interaction between the magnetite and CD. The thermal analysis was measured by thermogravimetric and differential thermal analysis (TGA-DTA). The magnetic properties, intrinsic coercivity (H{sub c}) and the saturation magnetization were determined by vibrating sample magnetometry (VSM); the size and shape of nanoparticles were determined by scanning electron microscopy (SEM). The identification of phases was made by X-ray diffraction.

  3. Synthesis, characterization, applications, and challenges of iron oxide nanoparticles

    Science.gov (United States)

    Ali, Attarad; Zafar, Hira; Zia, Muhammad; ul Haq, Ihsan; Phull, Abdul Rehman; Ali, Joham Sarfraz; Hussain, Altaf

    2016-01-01

    Recently, iron oxide nanoparticles (NPs) have attracted much consideration due to their unique properties, such as superparamagnetism, surface-to-volume ratio, greater surface area, and easy separation methodology. Various physical, chemical, and biological methods have been adopted to synthesize magnetic NPs with suitable surface chemistry. This review summarizes the methods for the preparation of iron oxide NPs, size and morphology control, and magnetic properties with recent bioengineering, commercial, and industrial applications. Iron oxides exhibit great potential in the fields of life sciences such as biomedicine, agriculture, and environment. Nontoxic conduct and biocompatible applications of magnetic NPs can be enriched further by special surface coating with organic or inorganic molecules, including surfactants, drugs, proteins, starches, enzymes, antibodies, nucleotides, nonionic detergents, and polyelectrolytes. Magnetic NPs can also be directed to an organ, tissue, or tumor using an external magnetic field for hyperthermic treatment of patients. Keeping in mind the current interest in iron NPs, this review is designed to report recent information from synthesis to characterization, and applications of iron NPs. PMID:27578966

  4. Synthesis of magnetite nanoparticles-β-cyclodextrin complex

    International Nuclear Information System (INIS)

    In this work, the synthesis and characterization of a magnetite (M) and β-cyclodextrin (CD) complex is presented. The chemical bonding between the magnetite and CD was studied as evidence of host-guest interaction; therefore the CD works like a reactor with the magnetite inside of it, as consequence the growth of the particle is restricted by the electrostatic interaction of M-CD complex. The particle size of the magnetite-cyclodextrin complex (M-CD) decreased 79.1% with 0.5% of CD. The average particle size of the M-CD complex was 10 nm. The saturation magnetization (σs) and intrinsic coercivity (Hc) increased 10% and 20%, respectively. In order to understand how the the CD affects the results obtained, the second derivate of remission function was obtained from the ultraviolet-visible spectra (UV-vis). Fourier transform infrared spectroscopy (FTIR) was used to elucidate the interaction between the magnetite and CD. The thermal analysis was measured by thermogravimetric and differential thermal analysis (TGA-DTA). The magnetic properties, intrinsic coercivity (Hc) and the saturation magnetization were determined by vibrating sample magnetometry (VSM); the size and shape of nanoparticles were determined by scanning electron microscopy (SEM). The identification of phases was made by X-ray diffraction

  5. Large-scale solvothermal synthesis of fluorescent carbon nanoparticles

    Science.gov (United States)

    Ku, Kahoe; Lee, Seung-Wook; Park, Jinwoo; Kim, Nayon; Chung, Haegeun; Han, Chi-Hwan; Kim, Woong

    2014-09-01

    The large-scale production of high-quality carbon nanomaterials is highly desirable for a variety of applications. We demonstrate a novel synthetic route to the production of fluorescent carbon nanoparticles (CNPs) in large quantities via a single-step reaction. The simple heating of a mixture of benzaldehyde, ethanol and graphite oxide (GO) with residual sulfuric acid in an autoclave produced 7 g of CNPs with a quantum yield of 20%. The CNPs can be dispersed in various organic solvents; hence, they are easily incorporated into polymer composites in forms such as nanofibers and thin films. Additionally, we observed that the GO present during the CNP synthesis was reduced. The reduced GO (RGO) was sufficiently conductive (σ ≈ 282 S m-1) such that it could be used as an electrode material in a supercapacitor; in addition, it can provide excellent capacitive behavior and high-rate capability. This work will contribute greatly to the development of efficient synthetic routes to diverse carbon nanomaterials, including CNPs and RGO, that are suitable for a wide range of applications.

  6. Synthesis of silver nanoparticles using A. indicum leaf extract and their antibacterial activity.

    Science.gov (United States)

    Ashokkumar, S; Ravi, S; Kathiravan, V; Velmurugan, S

    2015-01-01

    Green synthesis of silver nanoparticles has been achieved using environmentally acceptable plant extract. It is observed that Abutilon indicum leaf extract can reduce silver ions into silver nanoparticles within 15 min of reaction time. The formation and stability of the reduced silver nanoparticles in the colloidal solution were monitored by UV-Vis spectrophotometer analysis. The mean particle diameter of silver nanoparticles was calculated from the XRD pattern. FT-IR spectra of the leaf extract after the development of nanoparticles are determined to allow identification of possible functional groups responsible for the conversion of metal ions to metal nanoparticles. The AgNPs thus obtained showed highly potent antibacterial activity toward Gram-positive (Staphyloccocus aureus and Bacillus subtilis) and Gram-negative (Salmonella typhi and Escherichia coli) microorganisms. PMID:24997264

  7. The Green synthesis of gold nanoparticles using an aqueous root extract of Morinda citrifolia L

    Science.gov (United States)

    Suman, T. Y.; Radhika Rajasree, S. R.; Ramkumar, R.; Rajthilak, C.; Perumal, P.

    2014-01-01

    In the present work, we describe the synthesis of gold nanoparticles using an aqueous root extract of Morinda citrifolia. UV-vis spectroscopy, XRD, FTIR, FE-SEM, EDX and TEM were performed to characterize the formation of gold nanoparticles. The synthesized gold nanoparticles were characterized by a peak at 540 nm in the UV-vis spectrum. The XRD peaks at 38°, 44°, 64° and 77° can be indexed to the (1 1 1), (2 0 0), (2 2 0) and (3 1 1) Bragg's reflections of cubic structure of metallic gold, respectively. The FTIR result showed that extract containing protein might be responsible for the formation of the nanoparticles and may play an important role in the stabilization of the formed nanoparticles. FESEM images revealed that the particles were triangle and mostly spherical in shape. TEM images clearly revealed the size of the nanoparticles were 12.17-38.26 nm in size.

  8. Green synthesis of biocompatible gold nanoparticles using Fagopyrum esculentum leaf extract

    Science.gov (United States)

    Babu, Punuri Jayasekhar; Sharma, Pragya; Kalita, Mohan Chandra; Bora, Utpal

    2011-12-01

    This report describes the use of ethnolic extract of Fagopyrum esculentum leaves for the synthesis of gold nanoparticles. UV-visible spectroscopy analysis indicated the successful formation of gold nanoparticles. The synthesized nanoparticles were characterized by transmission electron microscopy (TEM), high resolution TEM (HRTEM) and were found to be spherical, hexagonal and triangular in shape with an average size of 8.3 nm. The crystalline nature of the gold nanoparticles was confirmed from X-ray diffraction (XRD) and selected-area electron diffraction (SAED) patterns. Fourier transform infrared (FT-IR) and energy-dispersive X-ray analysis (EDX) suggested the presence of organic biomolecules on the surface of the gold nanoparticles. Cytotoxicity tests against human HeLa, MCF-7 and IMR-32 cancer cell lines revealed that the gold nanoparticles were non-toxic and thus have potential for use in various biomedical applications.

  9. Opuntia ficus indica peel derived pectin mediated hydroxyapatite nanoparticles: Synthesis, spectral characterization, biological and antimicrobial activities

    Science.gov (United States)

    Gopi, D.; Kanimozhi, K.; Kavitha, L.

    2015-04-01

    In the present study, we have adapted a facile and efficient green route for the synthesis of HAP nanoparticles using pectin as a template which was extracted from the peel of prickly pear (Opuntia ficus indica) fruits. The concentration of pectin plays a major role in the behavior of crystallinity, purity, morphology as well as biological property of the as-synthesized HAP nanoparticles. The extracted pectin and the as-synthesized nanoparticles were characterized by various analytical techniques. The in vitro apatite formation on the surface of the as-synthesized nanoparticles in simulated body fluid (SBF) for various days showed an enhanced bioactivity. Also, the antimicrobial activity was investigated using various microorganisms. All the results revealed the formation of pure, low crystalline and discrete granular like HAP nanoparticles of size around 25 nm with enhanced biological and antimicrobial activities. Hence the as-synthesized nanoparticles can act as a better bone regenerating material in the field of biomedicine.

  10. Green hydrothermal synthesis and optical properties of γ-Gd2S3 nanoparticles

    Science.gov (United States)

    Khajuria, Sonika; Ladol, Jigmet; Sanotra, Sumit; Sheikh, Haq Nawaz

    2016-06-01

    Green synthesis of γ-Gd2S3 nanoparticles was carried out using low-temperature hydrothermal route in autoclave. A 1:1 mixture of ionic liquid 1-ethyl-3-methylimidazolium ethyl sulfate, ([EMIM][EtSO4]), and water was used as a solvent. Synthesized nanoparticles were characterized by x-ray powder diffraction (XRPD), scanning electron microscopy (SEM), UV-visible spectroscopy (UV-vis), particle size by dynamic light scattering (DLS) technique, and photoluminescence (PL) studies. XRPD suggests cubic Th3P4-type structure for obtained Gd2S3 nanoparticles. The size of synthesized nanoparticles is about 86 nm. Optical band gap for these nanoparticles estimated from electronic spectrum is 2.95 eV which shows blue shift from values reported for bulk Gd2S3 due to pronounced quantum mechanical effect. These nanoparticles show sharp emission peak at 385 nm and a broad shoulder at 475 nm when excited at 260 nm.

  11. A Novel Synthesis of Malic Acid Capped Silver Nanoparticles using Solanum lycopersicums Fruit Extract

    Institute of Scientific and Technical Information of China (English)

    M.Umadevi; M.R.Bindhu; V.Sathe

    2013-01-01

    Integration of green chemistry principles to nanotechnology is one of the key issues in nanoscience research.The development of the concept of green nanoparticle preparation has been growingly needed for environmentally benign metal nanoparticle synthesis protocols to avoid adverse effects in medical applications.Keep this in mind,in the present study,silver nanoparticles were synthesized using Solanum lycopersicums fruit extract.The prepared silver nanoparticles were characterized by UV-visible spectroscopy,Fourier transform infrared spectroscopy,Raman spectroscopy,scanning electron microscopy and transmission electron microscopy techniques.The surface plasmon resonance peak was found at 445 nm.The synthesized silver nanoparticles were spherical in shape with the average size of 10 nm.The citric acid present in S.lycopersicums fruit extract acted as reducing agent and malic acid was responsible for capping of the bioreduced silver nanoparticles.

  12. MZnFe{sub 2}O{sub 4} (M = Ni, Mn) cubic superparamagnetic nanoparticles obtained by hydrothermal synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Freire, R. M. [Universidade Federal do Ceara-UFC, Grupo de Quimica de Materiais Avancados (GQMAT)- Departamento de Quimica Analitica e Fisico-Quimica (Brazil); Ribeiro, T. S.; Vasconcelos, I. F. [Universidade Federal do Ceara, Departamento de Engenharia Metalurgica e de Materiais (Brazil); Denardin, J. C. [Universidad de Santiago de Chile, USACH, Departamento de Fisica (Chile); Barros, E. B. [Universidade Federal do Ceara-UFC, Departamento de Fisica (Brazil); Mele, Giuseppe [Universita del Salento, Dipartimento di Ingegneria dell' Innovazione (Italy); Carbone, L. [IPCF-CNR, UOS Pisa (Italy); Mazzetto, S. E.; Fechine, P. B. A., E-mail: fechine@ufc.br [Universidade Federal do Ceara-UFC, Grupo de Quimica de Materiais Avancados (GQMAT)- Departamento de Quimica Analitica e Fisico-Quimica (Brazil)

    2013-05-15

    MZnFe{sub 2}O{sub 4} (M = Ni or Mn) cubic nanoparticles have been prepared by hydrothermal synthesis in mild conditions and short time without any procedure of calcinations. The structural and magnetic properties of the mixed ferrites were investigated by X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, Moessbauer spectroscopy, vibrating sample magnetometer, and Transmission electron microscopy (TEM). X-ray analysis showed peaks characteristics of the spinel phase. The average diameter of the nanoparticles observed by TEM measurements was approximately between 4 and 10 nm. Spectroscopy study of the spinel structure was performed based on Group Theory. The predicted bands were observed in FTIR and Raman spectrum. The magnetic parameters and Moessbauer spectroscopy were measured at room temperature and superparamagnetic behavior was observed for mixed ferrites. This kind of nanoparticles can be used as precursor in drug delivery systems, magnetic hyperthermia, ferrofluids, or magnetic imaging contrast agents.

  13. Magnetic iron oxide nanoparticles: Synthesis and surface coating techniques for biomedical applications

    International Nuclear Information System (INIS)

    Iron oxide nanoparticles are the most popular magnetic nanoparticles used in biomedical applications due to their low cost, low toxicity, and unique magnetic property. Magnetic iron oxide nanoparticles, including magnetite (Fe3O4) and maghemite (γ-Fe2O3), usually exhibit a superparamagnetic property as their size goes smaller than 20 nm, which are often denoted as superparamagnetic iron oxide nanoparticles (SPIONs) and utilized for drug delivery, diagnosis, therapy, and etc. This review article gives a brief introduction on magnetic iron oxide nanoparticles in terms of their fundamentals of magnetism, magnetic resonance imaging (MRI), and drug delivery, as well as the synthesis approaches, surface coating, and application examples from recent key literatures. Because the quality and surface chemistry play important roles in biomedical applications, our review focuses on the synthesis approaches and surface modifications of iron oxide nanoparticles. We aim to provide a detailed introduction to readers who are new to this field, helping them to choose suitable synthesis methods and to optimize the surface chemistry of iron oxide nanoparticles for their interests. (topical review — magnetism, magnetic materials, and interdisciplinary research)

  14. Synthesis and Physicochemical Characterization of Mesoporous SiO2 Nanoparticles

    Directory of Open Access Journals (Sweden)

    Dharani Das

    2014-01-01

    Full Text Available There exists a knowledge gap in understanding potential toxicity of mesoporous silica nanoparticles. A critical step in assessing toxicity of these particles is to have a wide size range with different chemistries and physicochemical properties. There are several challenges when synthesizing mesoporous silica nanoparticles over a wide range of sizes including (1 nonuniform synthesis protocols using the same starting materials, (2 the low material yield in a single batch synthesis (especially for particles below 60–70 nm, and (3 morphological instability during surfactant removal process and surface modifications. In this study, we synthesized a library of mesoporous silica nanoparticles with approximate particle sizes of 25, 70, 100, 170, and 600 nm. Surfaces of the silica nanoparticles were modified with hydrophilic-CH2–(CH22–COOH and relatively hydrophobic-CH2–(CH210–COOH functional groups. All silica nanoparticles were analysed for morphology, surface functionality, surface area/pore volume, surface organic content, and dispersion characteristics in liquid media. Our analysis revealed the synthesis of a spectrum of monodisperse bare and surface modified mesoporous silica nanoparticles with a narrow particle size distribution and devoid of cocontaminants critical for toxicity studies. Complete physicochemical characterization of these synthetic mesoporous silica nanoparticles will permit systematic toxicology studies for investigation of structure-activity relationships.

  15. Synthesis of silver nanoparticles by using tea leaf extract from Camellia Sinensis

    Directory of Open Access Journals (Sweden)

    Loo YY

    2012-08-01

    Full Text Available Yuet Ying Loo,1 Buong Woei Chieng,2 Mitsuaki Nishibuchi,3 Son Radu11Centre of Excellent for Food Safety Research, Faculty of Food Science and Technology, Universiti Putra Malaysia, Selangor, Malaysia; 2Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, Selangor, Malaysia; 3Center for South East Asian Studies, Kyoto University, Kyoto, JapanAbstract: The development of the biological synthesis of nanoparticles using microorganisms or plant extracts plays an important role in the field of nanotechnology as it is environmentally friendly and does not involve any harmful chemicals. In this study, the synthesis of silver nanoparticles using the leaves extract of Chinese tea from Camellia sinensis is reported. The synthesized nanoparticles were characterized using UV-vis spectroscopy, X-ray diffraction (XRD, transmission electron microscopy (TEM, and Fourier transform infrared (FTIR spectroscopy. The XRD analysis shows that the synthesized silver nanoparticles are of face-centered cubic structure. Well-dispersed silver nanoparticles with an approximate size of 4 nm were observed in the TEM image. The application of the green synthesized nanoparticles can be used in many fields such as cosmetics, foods, and medicine.Keywords: silver, nanoparticles, green synthesis, leaf extract, transmission electron microscopy, nanotechnology

  16. Green synthesis of monodisperse silver nanoparticles using hydroxy propyl methyl cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Chunfa; Zhang, Xianglin, E-mail: hust_zxl@mail.hust.edu.cn; Cai, Hao

    2014-01-15

    Graphical abstract: -- Highlights: • Synthesis of silver nanoparticles using hydroxy propyl methyl cellulose is reported. • HPMC and glucose are used as capping agent and reducing agent respectively. • It is the first time to use HPMC for synthesis of silver nanoparticles. • The small, spherical and well-dispersed particle is observed in the range of 3–17 nm. • The green method can be extended to other noble metals. -- Abstract: A simple and environmentally friendly method for the synthesis of highly stable and small sized silver nanoparticles with narrow distribution from 3 nm to 17 nm is reported. Silver nitrate, hydroxy propyl methyl cellulose (HPMC) and glucose, were used as silver precursor, capping agents and reducing agents respectively. The formation of silver nanoparticles was observed by change of color from colorless to wine red. The silver nanoparticles were characterized by transmission electron microscopy (TEM), UV–visible spectroscopy (UV–vis), X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FT-IR). The results demonstrated that the obtained metallic nanoparticles were single crystalline silver nanoparticles capped with HPMC. The effects of the reaction time, reaction temperature and the concentration of silver ion and reducing agents on the particle size were investigated. A possible formation mechanism was proposed. The method may be extended to other noble metal for other technological applications such as additional medicinal, industrial applications.

  17. Raman Amplifier Based on Amorphous Silicon Nanoparticles

    OpenAIRE

    M.A. Ferrara; Rendina, I.; S. N. Basu; Dal Negro, L.; Sirleto, L.

    2012-01-01

    The observation of stimulated Raman scattering in amorphous silicon nanoparticles embedded in Si-rich nitride/silicon superlattice structures (SRN/Si-SLs) is reported. Using a 1427 nm continuous-wavelength pump laser, an amplification of Stokes signal up to 0.9 dB/cm at 1540.6 nm and a significant reduction in threshold power of about 40% with respect to silicon are experimentally demonstrated. Our results indicate that amorphous silicon nanoparticles are a great promise for Si-based Raman la...

  18. Alkaline Capacitors Based on Nitride Nanoparticles

    Science.gov (United States)

    Aldissi, Matt

    2003-01-01

    High-energy-density alkaline electrochemical capacitors based on electrodes made of transition-metal nitride nanoparticles are undergoing development. Transition- metal nitrides (in particular, Fe3N and TiN) offer a desirable combination of high electrical conductivity and electrochemical stability in aqueous alkaline electrolytes like KOH. The high energy densities of these capacitors are attributable mainly to their high capacitance densities, which, in turn, are attributable mainly to the large specific surface areas of the electrode nanoparticles. Capacitors of this type could be useful as energy-storage components in such diverse equipment as digital communication systems, implanted medical devices, computers, portable consumer electronic devices, and electric vehicles.

  19. Nanoparticle-based therapy for respiratory diseases

    Directory of Open Access Journals (Sweden)

    ADRIANA L. DA SILVA

    2013-03-01

    Full Text Available Nanotechnology is an emerging science with the potential to create new materials and strategies involving manipulation of matter at the nanometer scale (<100 nm. With size-dependent properties, nanoparticles have introduced a new paradigm in pharmacotherapy – the possibility of cell-targeted drug delivery with minimal systemic side effects and toxicity. The present review provides a summary of published findings, especially regarding to nanoparticle formulations for lung diseases. The available data have shown some benefits with nanoparticle-based therapy in the development of the disease and lung remodeling in respiratory diseases. However, there is a wide gap between the concepts of nanomedicine and the published experimental data and clinical reality. In addition, studies are still required to determine the potential of nanotherapy and the systemic toxicity of nanomaterials for future human use.

  20. Naturally occurring nanoparticles from English ivy: an alternative to metal-based nanoparticles for UV protection

    Directory of Open Access Journals (Sweden)

    Zhang Zhili

    2010-06-01

    Full Text Available Abstract Background Over the last decade safety concerns have arisen about the use of metal-based nanoparticles in the cosmetics field. Metal-based nanoparticles have been linked to both environmental and animal toxicity in a variety of studies. Perhaps the greatest concern involves the large amounts of TiO2 nanoparticles that are used in commercial sunscreens. As an alternative to using these potentially hazardous metal-based nanoparticles, we have isolated organic nanoparticles from English ivy (Hedera helix. In this study, ivy nanoparticles were evaluated for their potential use in sunscreens based on four criteria: 1 ability to absorb and scatter ultraviolet light, 2 toxicity to mammalian cells, 3 biodegradability, and 4 potential for diffusion through skin. Results Purified ivy nanoparticles were first tested for their UV protective effects using a standard spectrophotometric assay. Next the cell toxicity of the ivy nanoparticles was compared to TiO2 nanoparticles using HeLa cells. The biodegradability of these nanoparticles was also determined through several digestion techniques. Finally, a mathematical model was developed to determine the potential for ivy nanoparticles to penetrate through human skin. The results indicated that the ivy nanoparticles were more efficient in blocking UV light, less toxic to mammalian cells, easily biodegradable, and had a limited potential to penetrate through human skin. When compared to TiO2 nanoparticles, the ivy nanoparticles showed decreased cell toxicity, and were easily degradable, indicating that they provided a safer alternative to these nanoparticles. Conclusions With the data collected from this study, we have demonstrated the great potential of ivy nanoparticles as a sunscreen protective agent, and their increased safety over commonly used metal oxide nanoparticles.

  1. One-pot synthesis of stable colloidal solutions of MFe{sub 2}O{sub 4} nanoparticles using oleylamine as solvent and stabilizer

    Energy Technology Data Exchange (ETDEWEB)

    Pérez-Mirabet, Leonardo [Departament de Química, Universitat Autònoma de Barcelona, Campus de la UAB, 08193 Bellaterra (Spain); Solano, Eduardo, E-mail: eduardo.solano@uab.cat [Departament de Química, Universitat Autònoma de Barcelona, Campus de la UAB, 08193 Bellaterra (Spain); Martínez-Julián, Fernando; Guzmán, Roger [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain); Arbiol, Jordi [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain); Institució Catalana de Recerca i Estudis Avançats (ICREA), 08019 Barcelona (Spain); Puig, Teresa; Obradors, Xavier; Pomar, Alberto [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain); Yáñez, Ramón; Ros, Josep [Departament de Química, Universitat Autònoma de Barcelona, Campus de la UAB, 08193 Bellaterra (Spain); Ricart, Susagna [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain)

    2013-03-15

    Highlights: ► One-pot synthesis of ferrite magnetic nanoparticles (<10 nm) in non-polar media. ► Nanoparticles present high monocrystal quality and monodispersion. ► Superparamagnetic behavior at room temperature. ► Nanoparticles transfer to polar media via ligand exchange. - Abstract: An easy, efficient, reproducible and scalable one-pot synthetic methodology to obtain magnetic spinel ferrite nanoparticles has been developed. This approach is based on one-pot thermal decomposition of Fe(acac){sub 3} and M(acac){sub 2} (M = Co, Mn, Cu and Zn) in oleylamine, which also acts as a capping ligand, by producing stable colloidal dispersions of nanoparticles in non-polar solvents. The properties of the nanoparticles have been studied via different techniques, such as transmission electron microscopy, which shows that nanoparticles are monocrystallines and a narrow dispersion in size; magnetic analyses have demonstrated that the resulting ferrite nanoparticles show high saturation values and superparamagnetic behavior at room temperature; X-ray diffraction has also been performed, and it confirms that the synthesized nanoparticles have a spinel structure. Complementarily, ligand exchange has been also carried out in order to produce dispersions of the synthesized nanoparticles in polar media.

  2. Synthesis and thermal properties of new bionanofluids containing gold nanoparticles

    Science.gov (United States)

    Jiménez-Pérez, J. L.; López Gamboa, G.; Gutiérrez Fuentes, R.; Sánchez Ramírez, J. F.; Correa Pacheco, Z. N.; López-y-López, V. E.; Tepech-Carrillo, L.

    2016-10-01

    New bionanofluids containing Au nanoparticles with different concentrations were prepared by chemical reduction method. The nanoparticles were mixed with biodiesel from soybean prepared using alkaline catalysts. Thermal properties of biodiesel containing Au nanoparticles with different volume percentage concentrations were measured by mismatched dual-beam mode thermal lens technique in order to measure the effect of the presence of nanoparticles ( φ = 13.3 nm) on the bionanofluids thermal diffusivity. The characteristic time constant of the transient thermal lens was estimated by fitting the experimental data to the theoretical expression for transient thermal lens. The thermal diffusivity of the bionanofluids (biodiesel containing Au nanoparticles) seems to be strongly dependent on the presence of nanoparticles. It was observed an increase in the thermal diffusivity when volume percentage of nanoparticles increased. A possible explanation for such high thermal diffusivity of the biodiesel with Au nanoparticles is given. UV-Vis spectroscopy and TEM microscopy techniques were used to characterize the bionanofluids.

  3. Synthesis of aluminium nanoparticles by arc plasma spray under atmospheric pressure

    Energy Technology Data Exchange (ETDEWEB)

    Mandilas, Charalampos; Daskalos, Emmanouil [Aerosol and Particle Technology Laboratory (APTL), Chemical Process and Energy Resources Institute, Centre for Research and Technology-Hellas (CERTH/CPERI), P.O. Box 361, 57001 Thermi, Thessaloniki (Greece); Karagiannakis, George, E-mail: gkarag@cperi.certh.gr [Aerosol and Particle Technology Laboratory (APTL), Chemical Process and Energy Resources Institute, Centre for Research and Technology-Hellas (CERTH/CPERI), P.O. Box 361, 57001 Thermi, Thessaloniki (Greece); Konstandopoulos, Athanasios G., E-mail: agk@cperi.certh.gr [Aerosol and Particle Technology Laboratory (APTL), Chemical Process and Energy Resources Institute, Centre for Research and Technology-Hellas (CERTH/CPERI), P.O. Box 361, 57001 Thermi, Thessaloniki (Greece); Department of Chemical Engineering, Aristotle University, P.O. Box 1517, 54006 Thessaloniki (Greece)

    2013-01-01

    Highlights: Black-Right-Pointing-Pointer A customized arc-plasma spraying based system has been designed and implemented. Black-Right-Pointing-Pointer The system is relatively simple, robust and operates at atmospheric pressure. Black-Right-Pointing-Pointer Preparation of aluminium nanoparticles from micron-sized powder was successful. Black-Right-Pointing-Pointer Various nano-sized distributions were possible depending on operating parameters. Black-Right-Pointing-Pointer Optimization of the proposed design will lead to higher efficiencies and throughput. - Abstract: The present study addresses the feasibility to synthesize aluminium nanoparticles (NPs) from micron-sized aluminium powder with the use of a customized atmospheric plasma spraying (APS) technique. Using APS, nanoparticle synthesis can be achieved via rapid melting and vaporization of the initial micrometric particles and their subsequent re-nucleation. A custom mantle system was designed and developed with the aid of relevant simplified CFD simulations. The mantle provided the necessary inert environment (argon), at ambient pressure, in order to avoid any oxidation of the metal during plasma spraying while promoted rapid quenching of the gasified metal. The particles formed were collected with the aid of a quartz filter downstream of the plasma flame and the production rate achieved was 2 g min{sup -1}. Ex situ post-characterization of the particles via X-ray diffraction, specific surface area measurement (BET), transmission electron microscopy (TEM) coupled with energy dispersive spectrometry (EDS) and thermogravimetric analysis (TGA) under air revealed that the powders obtained primarily comprised of monocrystalline metallic aluminium nanoparticles of almost spherical shape. The NPs possessed a 2-5 nm oxide coating layer. By regulating the conditions inside the mantle, a variety of different size distributions were obtained.

  4. Continuous Polyol Synthesis of Metal and Metal Oxide Nanoparticles Using a Segmented Flow Tubular Reactor (SFTR

    Directory of Open Access Journals (Sweden)

    Andrea Testino

    2015-06-01

    Full Text Available Over the last years a new type of tubular plug flow reactor, the segmented flow tubular reactor (SFTR, has proven its versatility and robustness through the water-based synthesis of precipitates as varied as CaCO3, BaTiO3, Mn(1−xNixC2O4·2H2O, YBa oxalates, copper oxalate, ZnS, ZnO, iron oxides, and TiO2 produced with a high powder quality (phase composition, particle size, and shape and high reproducibility. The SFTR has been developed to overcome the classical problems of powder production scale-up from batch processes, which are mainly linked with mass and heat transfer. Recently, the SFTR concept has been further developed and applied for the synthesis of metals, metal oxides, and salts in form of nano- or micro-particles in organic solvents. This has been done by increasing the working temperature and modifying the particle carrying solvent. In this paper we summarize the experimental results for four materials prepared according to the polyol synthesis route combined with the SFTR. CeO2, Ni, Ag, and Ca3(PO42 nanoparticles (NPs can be obtained with a production rate of about 1–10 g per h. The production was carried out for several hours with constant product quality. These findings further corroborate the reliability and versatility of the SFTR for high throughput powder production.

  5. Influence of Synthesis Parameters on Magnetization and Size of Iron Oxide Nanoparticles

    Science.gov (United States)

    Lak, Aidin; Ludwig, Frank; Grabs, Ilka-Maria; Garnweitner, Georg; Schilling, Meinhard

    2010-12-01

    The effect of the synthesis parameters precursor concentration, reaction temperature, reaction time, and heating rate on the non-hydrolytic synthesis of iron oxide nanoparticles was studied via statistical design of experiment (DOE) methodology. The net sample magnetic moments were determined by fluxgate magnetorelaxometry (MRX). Multiple linear regression analysis provided an empirical model where the net magnetic moments solely depend on precursor concentration and reaction temperature. The correctness of net magnetic moments determined from MRX measurements was verified by static M-H measurements on three selected samples. Also, good agreement of the particle core sizes determined by TEM and by fitting static M-H curves with the Langevin function was found for these samples. A similar dependence on synthesis parameters was observed for sample core sizes and the net sample magnetic moments based on comparative measurements on the selected samples, indicating that the core sizes solely depend on precursor concentration and reaction temperature but not on reaction time and heating rate. On the other hand, an increase of reaction time causes a broadening of the core size distribution.

  6. Metal-doped semiconductor nanoparticles and methods of synthesis thereof

    Science.gov (United States)

    Ren, Zhifeng (Inventor); Chen, Gang (Inventor); Poudel, Bed (Inventor); Kumar, Shankar (Inventor); Wang, Wenzhong (Inventor); Dresselhaus, Mildred (Inventor)

    2009-01-01

    The present invention generally relates to binary or higher order semiconductor nanoparticles doped with a metallic element, and thermoelectric compositions incorporating such nanoparticles. In one aspect, the present invention provides a thermoelectric composition comprising a plurality of nanoparticles each of which includes an alloy matrix formed of a Group IV element and Group VI element and a metallic dopant distributed within the matrix.

  7. Green Chemistry Approach for the Synthesis of Gold Nanoparticles Using the Fungus Alternaria sp.

    Science.gov (United States)

    Dhanasekar, Naresh Niranjan; Rahul, Ganga Ravindran; Narayanan, Kannan Badri; Raman, Gurusamy; Sakthivel, Natarajan

    2015-07-01

    The synthesis of gold nanoparticles has gained tremendous attention owing to their immense applications in the field of biomedical sciences. Although several chemical procedures are used for the synthesis of nanoparticles, the release of toxic and hazardous by-products restricts their use in biomedical applications. In the present investigation, gold nanoparticles were synthesized biologically using the culture filtrate of the filamentous fungus Alternaria sp. The culture filtrate of the fungus was exposed to three different concentrations of chloroaurate ions. In all cases, the gold ions were reduced to Au(0), leading to the formation of stable gold nanoparticles of variable sizes and shapes. UV-Vis spectroscopy analysis confirmed the formation of nanoparticles by reduction of Au(3+) to Au(0). TEM analysis revealed the presence of spherical, rod, square, pentagonal, and hexagonal morphologies for 1 mM chloroaurate solution. However, quasi-spherical and spherical nanoparticles/heart-like morphologies with size range of about 7-13 and 15-18 nm were observed for lower molar concentrations of 0.3 and 0.5 mM gold chloride solution, respectively. The XRD spectrum revealed the face-centered cubic crystals of synthesized gold nanoparticles. FT-IR spectroscopy analysis confirmed the presence of aromatic primary amines, and the additional SPR bands at 290 and 230 nm further suggested that the presence of amino acids such as tryptophan/tyrosine or phenylalanine acts as the capping agent on the synthesized mycogenic gold nanoparticles.

  8. Green synthesis of gold nanoparticles using Stevia rebaudiana leaf extracts: Characterization and their stability.

    Science.gov (United States)

    Sadeghi, Babak; Mohammadzadeh, M; Babakhani, B

    2015-07-01

    Various methods invented and developed for the synthesis of gold nanoparticles that increases daily consumed. According to this method, including potential environmental pollution problems and the complexity of the synthesis, in this study, the feasibility of using the leaves extract of Stevia rebaudiana (SR) for the reduction of gold ions to nanoparticles form have been studied. Stevia leaves were used to prepare the aqueous extract for this study. Gold nanoparticles were characterized with different techniques such as UV-vis spectroscopy, FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Transmission electron microscopy experiments showed that these nanoparticles are spherical and uniformly distributed and its size is from 5 to 20 nm. FT-IR spectroscopy revealed that gold nanoparticles were functionalized with biomolecules that have primary amine group (NH2), carbonyl group, OH groups and other stabilizing functional groups. X-ray diffraction pattern showed high purity and face centered cubic structure of gold nanoparticles with size of 17 nm. The scanning electron microscopy (SEM) implies the right of forming gold nanoparticles. The results, confirm that gold nanoparticles have synthesized by the leaves extract of S. rebaudiana (SR).

  9. Green Chemistry Approach for the Synthesis of Gold Nanoparticles Using the Fungus Alternaria sp.

    Science.gov (United States)

    Dhanasekar, Naresh Niranjan; Rahul, Ganga Ravindran; Narayanan, Kannan Badri; Raman, Gurusamy; Sakthivel, Natarajan

    2015-07-01

    The synthesis of gold nanoparticles has gained tremendous attention owing to their immense applications in the field of biomedical sciences. Although several chemical procedures are used for the synthesis of nanoparticles, the release of toxic and hazardous by-products restricts their use in biomedical applications. In the present investigation, gold nanoparticles were synthesized biologically using the culture filtrate of the filamentous fungus Alternaria sp. The culture filtrate of the fungus was exposed to three different concentrations of chloroaurate ions. In all cases, the gold ions were reduced to Au(0), leading to the formation of stable gold nanoparticles of variable sizes and shapes. UV-Vis spectroscopy analysis confirmed the formation of nanoparticles by reduction of Au(3+) to Au(0). TEM analysis revealed the presence of spherical, rod, square, pentagonal, and hexagonal morphologies for 1 mM chloroaurate solution. However, quasi-spherical and spherical nanoparticles/heart-like morphologies with size range of about 7-13 and 15-18 nm were observed for lower molar concentrations of 0.3 and 0.5 mM gold chloride solution, respectively. The XRD spectrum revealed the face-centered cubic crystals of synthesized gold nanoparticles. FT-IR spectroscopy analysis confirmed the presence of aromatic primary amines, and the additional SPR bands at 290 and 230 nm further suggested that the presence of amino acids such as tryptophan/tyrosine or phenylalanine acts as the capping agent on the synthesized mycogenic gold nanoparticles. PMID:25737119

  10. Green synthesis of gold nanoparticles using Stevia rebaudiana leaf extracts: Characterization and their stability.

    Science.gov (United States)

    Sadeghi, Babak; Mohammadzadeh, M; Babakhani, B

    2015-07-01

    Various methods invented and developed for the synthesis of gold nanoparticles that increases daily consumed. According to this method, including potential environmental pollution problems and the complexity of the synthesis, in this study, the feasibility of using the leaves extract of Stevia rebaudiana (SR) for the reduction of gold ions to nanoparticles form have been studied. Stevia leaves were used to prepare the aqueous extract for this study. Gold nanoparticles were characterized with different techniques such as UV-vis spectroscopy, FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Transmission electron microscopy experiments showed that these nanoparticles are spherical and uniformly distributed and its size is from 5 to 20 nm. FT-IR spectroscopy revealed that gold nanoparticles were functionalized with biomolecules that have primary amine group (NH2), carbonyl group, OH groups and other stabilizing functional groups. X-ray diffraction pattern showed high purity and face centered cubic structure of gold nanoparticles with size of 17 nm. The scanning electron microscopy (SEM) implies the right of forming gold nanoparticles. The results, confirm that gold nanoparticles have synthesized by the leaves extract of S. rebaudiana (SR). PMID:25900555

  11. Gold-Pluronic core-shell nanoparticles: synthesis, characterization and biological evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Simon, Timea; Boca, Sanda [Babes-Bolyai University, Nanobiophotonics and Laser Microspectroscopy Center, Interdisciplinary Research Institute on Bio-Nano-Sciences and Faculty of Physics (Romania); Biro, Dominic [Sapientia University, Department of Mechanical Engineering, Faculty of Technical and Human Sciences (Romania); Baldeck, Patrice [Universite Joseph Fourier and CNRS, Laboratoire Interdisciplinaire de Physique, UMR 5588, CNRS (France); Astilean, Simion, E-mail: simion.astilean@phys.ubbcluj.ro [Babes-Bolyai University, Nanobiophotonics and Laser Microspectroscopy Center, Interdisciplinary Research Institute on Bio-Nano-Sciences and Faculty of Physics (Romania)

    2013-04-15

    This study presents the synthesis of gold-Pluronic core-shell nanoparticles by a two-step method and investigates their biological impact on cancer cells, specifically nanoparticle internalization and cytotoxicity. Uniform, 9-10-nm-sized, hydrophobic gold nanoparticles were synthesized in organic phase by reducing gold salt with oleylamine, after which oleylamine-protected gold nanoparticles were phase-transferred into aqueous medium using Pluronic F127 block copolymer, resulting in gold-Pluronic core-shell nanoparticles with a mean hydrodynamic diameter of {approx}35 nm. The formation and phase-transfer of gold nanoparticles were analyzed by UV-Vis absorption spectroscopy, transmission electron microscopy, and dynamic light scattering. The obtained gold-Pluronic core-shell nanoparticles proved to be highly stable in salted solution. Cytotoxicity tests showed no modification of cellular viability in the presence of properly purified particles. Furthermore, dark-field cellular imaging demonstrated that gold-Pluronic nanoparticles were able to be efficiently uptaken by cells, being internalized through nonspecific endocytosis. The high stability, proven biocompatibility, and imaging properties of gold-Pluronic core-shell nanoparticles hold promise for relevant intracellular applications, with such a design providing the feasibility to combine all multiple functionalities in one nanoparticle for simultaneous detection and imaging.

  12. Synthesis of silver nanoparticles by sophorolipids: Effect of temperature and sophorolipid structure on the size of particles

    Indian Academy of Sciences (India)

    M B Kasture; P Patel; A A Prabhune; C V Ramana; A A Kulkarni; B L V Prasad

    2008-11-01

    We report in situ synthesis of silver nanoparticles using biosurfactants called sophorolipids as reducing and capping agents. We further study the effect of temperature and the structure of sophorolipid on the size of silver nanoparticles obtained. The silver nanoparticles were characterized by UVvisible, transmission electron microscope (TEM) and light scattering (DLS) analysis techniques.

  13. A facile and rapid method for the black pepper leaf mediated green synthesis of silver nanoparticles and the antimicrobial study

    Science.gov (United States)

    Augustine, Robin; Kalarikkal, Nandakumar; Thomas, Sabu

    2014-10-01

    Green synthesis of nanoparticles is widely accepted due to the less toxicity in comparison with chemical methods. But there are certain drawbacks like slow formation of nanoparticles, difficulty to control particle size and shape make them less convenient. Here we report a novel cost-effective and eco-friendly method for the rapid green synthesis of silver nanoparticles using leaf extracts of Piper nigrum. Our results suggest that this method can be used for obtaining silver nanoparticles with controllable size within a few minutes. The fabricated nanoparticles possessed excellent antibacterial property against both Gram-positive and Gram-negative bacteria.

  14. Gaining Control over Radiolytic Synthesis of Uniform Sub-3-nanometer Palladium Nanoparticles: Use of Aromatic Liquids in the Electron Microscope.

    Science.gov (United States)

    Abellan, Patricia; Parent, Lucas R; Al Hasan, Naila; Park, Chiwoo; Arslan, Ilke; Karim, Ayman M; Evans, James E; Browning, Nigel D

    2016-02-16

    Synthesizing nanomaterials of uniform shape and size is of critical importance to access and manipulate the novel structure-property relationships arising at the nanoscale, such as catalytic activity. In this work, we synthesize Pd nanoparticles with well-controlled size in the sub-3 nm range using scanning transmission electron microscopy (STEM) in combination with an in situ liquid stage. We use an aromatic hydrocarbon (toluene) as a solvent that is very resistant to high-energy electron irradiation, which creates a net reducing environment without the need for additives to scavenge oxidizing radicals. The primary reducing species is molecular hydrogen, which is a widely used reductant in the synthesis of supported metal catalysts. We propose a mechanism of particle formation based on the effect of tri-n-octylphosphine (TOP) on size stabilization, relatively low production of radicals, and autocatalytic reduction of Pd(II) compounds. We combine in situ STEM results with insights from in situ small-angle X-ray scattering (SAXS) from alcohol-based synthesis, having similar reduction potential, in a customized microfluidic device as well as ex situ bulk experiments. This has allowed us to develop a fundamental growth model for the synthesis of size-stabilized Pd nanoparticles and demonstrate the utility of correlating different in situ and ex situ characterization techniques to understand, and ultimately control, metal nanostructure synthesis. PMID:26741639

  15. Gaining Control over Radiolytic Synthesis of Uniform Sub-3-nanometer Palladium Nanoparticles: Use of Aromatic Liquids in the Electron Microscope.

    Science.gov (United States)

    Abellan, Patricia; Parent, Lucas R; Al Hasan, Naila; Park, Chiwoo; Arslan, Ilke; Karim, Ayman M; Evans, James E; Browning, Nigel D

    2016-02-16

    Synthesizing nanomaterials of uniform shape and size is of critical importance to access and manipulate the novel structure-property relationships arising at the nanoscale, such as catalytic activity. In this work, we synthesize Pd nanoparticles with well-controlled size in the sub-3 nm range using scanning transmission electron microscopy (STEM) in combination with an in situ liquid stage. We use an aromatic hydrocarbon (toluene) as a solvent that is very resistant to high-energy electron irradiation, which creates a net reducing environment without the need for additives to scavenge oxidizing radicals. The primary reducing species is molecular hydrogen, which is a widely used reductant in the synthesis of supported metal catalysts. We propose a mechanism of particle formation based on the effect of tri-n-octylphosphine (TOP) on size stabilization, relatively low production of radicals, and autocatalytic reduction of Pd(II) compounds. We combine in situ STEM results with insights from in situ small-angle X-ray scattering (SAXS) from alcohol-based synthesis, having similar reduction potential, in a customized microfluidic device as well as ex situ bulk experiments. This has allowed us to develop a fundamental growth model for the synthesis of size-stabilized Pd nanoparticles and demonstrate the utility of correlating different in situ and ex situ characterization techniques to understand, and ultimately control, metal nanostructure synthesis.

  16. Synthesis and photo physical properties of Au - Ag (core - shell) nanoparticles disperse in poly vinyl alcohol matrix

    International Nuclear Information System (INIS)

    Synthesis of core - shell (Au - Ag) nanoparticle with varying silver composition has been carried out in aqueous poly vinyl alcohol (PVA) matrix. Core gold nanoparticle (∼15 nm) has been synthesized through seed-mediated growth process. Synthesis of silver shell with increasing thickness (∼1–5 nm) has been done by reducing Ag+ over the gold sol in the presence of mild reducing ascorbic acid. Characterization of Au - Ag nanoparticles has been done by UV–Vis, High resolution transmission electron microscope (HRTEM) and energy dispersive X-ray (EDX) spectroscopic study. The blue shift of surface plasmon resonance (SPR) band with increasing mole fraction of silver has been interpreted due to dampening of core, i.e. Au SPR by Ag. The dependence of nonlinear optical response of spherical core - shell nanoparticles has been investigated as a function of relative composition of each metal. Simulation of SPR extinction spectra based on quasi-static theory is done. A comparison of our experimental and the simulated extinction spectra using quasi-static theory of nanoshell suggests that our synthesized bimetallic particles have core - shell structure rather than bimetallic alloy particles.

  17. One step synthesis of Al/N co-doped carbon nanoparticles with enhanced photoluminescence

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Li; Ruan, Fengping; Lv, Ting; Liu, Yanqiang; Deng, Degang, E-mail: dengdegang@cjlu.edu.cn; Zhao, Shilong; Wang, Huanping; Xu, Shiqing, E-mail: sxucjlu@hotmail.com

    2015-02-15

    In a typical synthesis, luminescent carbon nanoparticles were synthesized via hydrothermal oxidation of glucose in deionized water. Here we reported the photoluminescence of the carbon nanoparticles greatly enhanced when reacted with Al(NO{sub 3}){sub 3} for the first time, the resulted carbon dots have appropriate spherical morphology, uniform size and good dispersion. The carbon nanoparticles can exhibit excitation-dependent photoluminescence behavior and emit bright green photoluminescence under UV excitation, which might provide a potential application for carbon dots in other extensive fields. - Highlights: • One step synthesis of Al/N co-doped carbon nanoparticles via a hydrothermal method. • The Al/N co-doped carbon dots possessed higher luminescence than the primordial one. • The cause for the enhanced photoluminescence was investigated and discussed.

  18. Mimusops elengi bark extract mediated green synthesis of gold nanoparticles and study of its catalytic activity

    Science.gov (United States)

    Majumdar, Rakhi; Bag, Braja Gopal; Ghosh, Pooja

    2016-04-01

    The bark extract of Mimusops elengi is rich in different types of plant secondary metabolites such as flavonoids, tannins, triterpenoids and saponins. The present study shows the usefulness of the bark extract of Mimusops elengi for the green synthesis of gold nanoparticles in water at room temperature under very mild conditions. The synthesis of the gold nanoparticles was complete within a few minutes without any extra stabilizing or capping agents and the polyphenols present in the bark extract acted as both reducing as well as stabilizing agents. The synthesized colloidal gold nanoparticles were characterized by HRTEM, surface plasmon resonance spectroscopy and X-ray diffraction studies. The synthesized gold nanoparticles have been used as an efficient catalyst for the reduction of 3-nitrophenol and 4-nitrophenol to their corresponding aminophenols in water at room temperature.

  19. Controlled green synthesis of silver nanoparticles by Allium cepa and Musa acuminata with strong antimicrobial activity

    Science.gov (United States)

    Sahni, Geetika; Panwar, Amit; Kaur, Balpreet

    2015-02-01

    A controlled "green synthesis" approach to synthesize silver nanoparticles by Allium cepa and Musa acuminata plant extract has been reported. The effect of different process parameters, such as pH, temperature and time, on synthesis of Ag nanoparticles from plant extracts has been highlighted. The work reports an easy approach to control the kinetics of interaction of metal ions with reducing agents, stabilized by ammonia to achieve sub-10 nm particles with narrow size distribution. The nanoparticles have been characterized by UV-Visible spectra and TEM analysis. Excellent antimicrobial activity at extremely low concentration of the nanoparticles was observed against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis and Fusarium oxysporum which may allow their exploitation as a new generation nanoproduct in biomedical and agricultural applications.

  20. Microbial synthesis of silver nanoparticles by Streptomyces glaucus and Spirulina platensis

    International Nuclear Information System (INIS)

    For the first time in Georgia a novel actinomycete strain Streptomyces glaucus 71 MD isolated from a soy rhizosphere has been used for microbial synthesis of silver nanoparticles. The Transmission Electron Microscopy (TEM) images revealed that most of the particles produced by these microorganisms from AgNO3 are spherical-like in shape with an average size of 13 nm. The Scanning Electron Microscope (SEM) allowed one to observe extracellular synthesis of nanoparticles, which has many advantages from the point of view of applications. Production of silver nanoparticles proceeds extracellularly with the participation of another microorganism, blue-green microalgae Spirulina platensis. It is shown that the production rate of the nanoparticles depends not only on the initial concentration of AgNO3 but also varies with time in a no monotonic way

  1. Green synthesis and characterization of silver nanoparticles using Cydonia oblong seed extract

    Science.gov (United States)

    Zia, Faria; Ghafoor, Nida; Iqbal, Mudassir; Mehboob, Saliha

    2016-10-01

    The green synthesis of nanoparticles has emerged as a cost-effective and environmentally benign technique. The present study describes the synthesis of silver nanoparticles (Ag-NPs) using a seed extract of Cydonia oblonga. The conditions were optimized by adjusting pH, temperature, time and amount of seed extract. The nanoparticles produced were characterized by different techniques, namely UV-visible spectroscopy, Fourier transmission infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy. The formation of Ag-NPs was confirmed by UV-visible spectroscopic analysis. FTIR analysis was performed to identify the biomolecules, which played a key role in the reduction of Ag+ ions. XRD confirmed that the silver nanoparticles possessed face-centered cubic structure. The green chemistry approach has proven that Ag-NPs can be synthesized by using plant extract in which biomolecules effectively act as capping and reducing agent.

  2. Green synthesis and characterization of silver nanoparticles using Cydonia oblong seed extract

    Science.gov (United States)

    Zia, Faria; Ghafoor, Nida; Iqbal, Mudassir; Mehboob, Saliha

    2016-01-01

    The green synthesis of nanoparticles has emerged as a cost-effective and environmentally benign technique. The present study describes the synthesis of silver nanoparticles (Ag-NPs) using a seed extract of Cydonia oblonga. The conditions were optimized by adjusting pH, temperature, time and amount of seed extract. The nanoparticles produced were characterized by different techniques, namely UV-visible spectroscopy, Fourier transmission infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy. The formation of Ag-NPs was confirmed by UV-visible spectroscopic analysis. FTIR analysis was performed to identify the biomolecules, which played a key role in the reduction of Ag+ ions. XRD confirmed that the silver nanoparticles possessed face-centered cubic structure. The green chemistry approach has proven that Ag-NPs can be synthesized by using plant extract in which biomolecules effectively act as capping and reducing agent.

  3. UNIFORM TiO2 NANOPARTICLES SYNTHESIS AND CHARACTERIZATION BY THERMOLYSIS PROCESS

    Directory of Open Access Journals (Sweden)

    DEBASHREE BHAKAT

    2012-07-01

    Full Text Available In this communication we present a versatile technique to synthesis spherical TiO2 nanoparticles by thermolysis process. Nanometer-sized Titania particles have been prepared by chemical reactions between Titanium tetrachloride and double distilled water in presence of hydrochloric acid. The size of the particles formed varied in the range of 100 to 300 nm and the morphology of the nanoparticles is spherical in shape having nanorods like structure on the surface of nanoparticles. The shape, size and structure of titanium dioxide products depends on the heating time and the quantity of titanium tetrachloride used in the reaction the powders were analyzed byUV-VIS spectroscopy and X-ray diffraction (XRD and Scanning electron microscopy observation was used for agglomerate observations. In the present research work, the important synthesis issues and applications of these nanoparticles are discussed in detail.

  4. Photosensitized synthesis of silver nanoparticles using Withania somnifera leaf powder and silver nitrate.

    Science.gov (United States)

    Raut, Rajesh Warluji; Mendhulkar, Vijay Damodhar; Kashid, Sahebrao Balaso

    2014-03-01

    The metal nanoparticle synthesis is highly explored field of nanotechnology. The biological methods seem to be more effective; however, due to slow reduction rate and polydispersity of the resulting products, they are less preferred. In the present study, we report rapid and facile synthesis of silver nanoparticles at room temperature. The exposure of reaction mixtures containing silver nitrate and dried leaf powder of Withania somnifera Linn to direct sunlight resulted in reduction of metal ions within five minutes whereas, the dark exposure took almost 12h. Further studies using different light filters reveal the role of blue light in reduction of silver ions. The synthesized silver nanoparticles were characterized by UV-Vis, Infrared spectroscopy (IR), Transmission Electron Microscopy (TEM), X-ray Diffraction studies (XRD), Nanoparticle Tracking Analysis (NTA), Energy Dispersive Spectroscopy (EDS), and Cyclic Voltammetry (CV). The Antibacterial and antifungal studies showed significant activity as compared to their respective standards.

  5. Shape-control by microwave-assisted hydrothermal method for the synthesis of magnetite nanoparticles using organic additives

    Energy Technology Data Exchange (ETDEWEB)

    Rizzuti, Antonino [Politecnico di Bari, Dipartimento di Ingegneria Civile, Ambientale, del Territorio, Edile e di Chimica (Italy); Dassisti, Michele [Politecnico di Bari, Dipartimento di Meccanica, Management e Matematica (Italy); Mastrorilli, Piero, E-mail: p.mastrorilli@poliba.it [Politecnico di Bari, Dipartimento di Ingegneria Civile, Ambientale, del Territorio, Edile e di Chimica (Italy); Sportelli, Maria C.; Cioffi, Nicola; Picca, Rosaria A. [Università di Bari, Dipartimento di Chimica (Italy); Agostinelli, Elisabetta; Varvaro, Gaspare [Consiglio Nazionale delle Ricerche, Istituto di Struttura della Materia (Italy); Caliandro, Rocco [Consiglio Nazionale delle Ricerche, Istituto di Cristallografia (Italy)

    2015-10-15

    A simple and fast microwave-assisted hydrothermal method is proposed for the synthesis of magnetite nanoparticles. The addition of different surfactants (polyvinylpyrrolidone, oleic acid, or trisodium citrate) was studied to investigate the effect on size distribution, morphology, and functionalization of the magnetite nanoparticles. Microwave irradiation at 150 °C for 2 h of aqueous ferrous chloride and hydrazine without additives resulted in hexagonal magnetite nanoplatelets with a facet-to-facet distance of 116 nm and a thickness of 40 nm having a saturation magnetization of ∼65 Am{sup 2} kg{sup −1}. The use of polyvinylpyrrolidone led to hexagonal nanoparticles with a facet-to-facet distance of 120 nm and a thickness of 53 nm with a saturation magnetization of ∼54 Am{sup 2} kg{sup −1}. Additives such as oleic acid and trisodium citrate yielded quasi-spherical nanoparticles of 25 nm in size with a saturation magnetization of ∼70 Am{sup 2} kg{sup −1} and spheroidal nanoparticles of 60 nm in size with a saturation magnetization up to ∼82 Am{sup 2} kg{sup −1}, respectively. A kinetic control of the crystal growth is believed to be responsible for the hexagonal habit of the nanoparticles obtained without additive. Conversely, a thermodynamic control of the crystal growth, leading to spheroidal nanoparticles, seems to occur when additives which strongly interact with the nanoparticle surface are used. A thorough characterization of the materials was performed. Magnetic properties were investigated by Superconducting Quantum Interference Device and Vibrating Sample magnetometers. Based on the observed magnetic properties, the magnetite obtained using citrate appears to be a promising support for magnetically transportable catalysts.

  6. Chrysopogon zizanioides aqueous extract mediated synthesis characterization of crystalline silver and gold nanoparticles for biomedical applications

    OpenAIRE

    Arunachalam KD; Annamalai SK

    2013-01-01

    Kantha D Arunachalam, Sathesh Kumar Annamalai Center for Environmental Nuclear Research, Directorate of Research, SRM University, Chennai, Tamil Nadu, India Abstract: The exploitation of various plant materials for the biosynthesis of nanoparticles is considered a green technology as it does not involve any harmful chemicals. The aim of this study was to develop a simple biological method for the synthesis of silver and gold nanoparticles using Chrysopogon zizanioides. To exploit various pla...

  7. Characterization of Silver Nanoparticle In Situ Synthesis on Porous Sericin Gel for Antibacterial Application

    OpenAIRE

    Gang Tao; Lina Liu; Yejing Wang; Huaipu Chang; Ping Zhao; Hua Zuo; Huawei He

    2016-01-01

    Sericin from Bombyx mori cocoon has good hydrophilicity, reaction activity, biocompatibility, and biodegradability, which has shown great potentials for biomedical materials. Here, an ultraviolet light-assisted in situ synthesis approach is developed to immobilize silver nanoparticles on the surface of sericin gel. The amount of silver nanoparticles immobilized on the surface of sericin gel could be regulated by the irradiation time. The porous structure and property of sericin gel were not a...

  8. Synthesis of highly-confined CdS nanoparticles by copolymerization of acryloylated starch

    OpenAIRE

    Mohammed, Aliyu D.; Onwudiwe, Damian C.; Young, Desmond A.; Vosloo, Hermanus C M

    2014-01-01

    A simple method for the synthesis of highly-confined and monodispersed, polyacryloylated starch-capped CdS nanoparticles (PAS-CdS) is reported. The synthesized nanoparticles exhibited a strong quantum confinement effect with respect to the bulk sample. Fourier transform infrared spectra confirmed the presence of acryloylated starch (AS) as a passivating agent. Transmission electron microscopy indicated that the particles were well dispersed and spherical in shape http://www.journals.elsevi...

  9. 3D CFD Simulations of MOCVD Synthesis System of Titanium Dioxide Nanoparticles

    OpenAIRE

    Siti Hajar Othman; Suraya Abdul Rashid; Tinia Idaty Mohd Ghazi; Norhafizah Abdullah

    2013-01-01

    This paper presents the 3-dimensional (3D) computational fluid dynamics (CFD) simulation study of metal organic chemical vapor deposition (MOCVD) producing photocatalytic titanium dioxide (TiO2) nanoparticles. It aims to provide better understanding of the MOCVD synthesis system especially of deposition process of TiO2 nanoparticles as well as fluid dynamics inside the reactor. The simulated model predicts temperature, velocity, gas streamline, mass fraction of reactants and products, kinetic...

  10. High-efficiency synthesis of nanoparticles in a repetitive multigap spark discharge generator

    Science.gov (United States)

    Ivanov, V. V.; Efimov, A. A.; Mylnikov, D. A.; Lizunova, A. A.; Bagazeev, A. V.; Beketov, I. V.; Shcherbinin, S. V.

    2016-08-01

    We describe a method of obtaining aerosol nanoparticles in a repetitive spark discharge generator with 12 interelectrode gaps between tin electrodes, which operates at a pulse repetition frequency of 2.5 kHz. During synthesis of tin oxide nanoparticles in air, the mass productivity of the gas discharge generator reaches up to 9 g/h for primary particles with characteristic sizes within 5-10 nm and agglomerate size on the order of 50 nm.

  11. An expeditious synthesis of early transition metal carbide nanoparticles on graphitic carbons.

    Science.gov (United States)

    Ressnig, Debora; Moldovan, Simona; Ersen, Ovidiu; Beaunier, Patricia; Portehault, David; Sanchez, Clément; Carenco, Sophie

    2016-08-01

    An expeditious synthesis of metal carbide nanoparticles onto various carbon supports is demonstrated. The procedure is versatile and readily yields TiC, VC, Mo2C and W2C nanoparticles on different types of carbons. The reaction is initiated at room temperature and proceeds within seconds. This novel synthetic route paves the way for a large variety of metal carbide-carbon nanocomposites that may be implemented in emerging nanotechnology fields.

  12. Memecylon edule leaf extract mediated green synthesis of silver and gold nanoparticles

    OpenAIRE

    Elavazhagan T; Arunachalam KD

    2011-01-01

    Tamizhamudu Elavazhagan, Kantha D ArunachalamCentre for Interdisciplinary Research, Directorate of Research, SRM University, Kattankulathur-603203, Tamilnadu, IndiaAbstract: We used an aqueous leaf extract of Memecylon edule (Melastomataceae) to synthesize silver and gold nanoparticles. To our knowledge, this is the first report where M. edule leaf broth was found to be a suitable plant source for the green synthesis of silver and gold nanoparticles. On treatment of aqueous solutions of silve...

  13. Gold and silver nanoparticles from Trianthema decandra: synthesis, characterization, and antimicrobial properties

    OpenAIRE

    Geethalakshmi R; Sarada DV

    2012-01-01

    R Geethalakshmi, DVL SaradaDepartment of Biotechnology, School of Bioengineering, Sri Ramaswamy Memorial University, Kattankulathur, Tamil Nadu, IndiaBackground: There is an increasing commercial demand for nanoparticles due to their wide applicability in various markets, including medicine, catalysis, electronics, chemistry, and energy. In this report, a simple and ecofriendly chemical reaction for the synthesis of gold and silver nanoparticles from Trianthema decandra (Aizoaceae) has been d...

  14. Synthesis and Surface Modification of Group IV Nanoparticles Using Non-Thermal Plasmas

    OpenAIRE

    Yasar-Inceoglu, Ozgul

    2015-01-01

    The rapidly increasing interest in silicon nanostructures is motivated by important advantages of this material compared to other semiconductors commonly investigated in the broad field of nanotechnology. Silicon nanoparticles are promising materials for many applications such as photovoltaics, transistors, light emitting devices, and energy storage devices. Commonly used nanoparticle synthesis techniques have many challenges such as high cost, long processing time, and wide particle size dis...

  15. SYNTHESIS AND CHARACTERIZATION OF GOLD NANOPARTICLES BY JUSTICIA GENDARUSSA BURM F. LEAF EXTRACT

    OpenAIRE

    Ponnuswamy Renuka Devi et al.

    2012-01-01

    The unusual physio and chemical properties of gold nanoparticles are found to have more advantage in the field of medicine, diagnostics and biosensors. In the present document, it is reported that Justicia gendarussa leaf extract mediated synthesis of gold nanoparticles by the reduction of gold ions. Three different phytochemical fractions were prepared from methanolic leaf extract by liquid-liquid extraction method using immiscible solvents. The total polyphenols, flavonoids and electron d...

  16. The synthesis of spinel ferrite nanoparticles using precipitation in microemulsions for ferrofluid applications

    Science.gov (United States)

    Makovec, Darko; Košak, Aljoša; Žnidaršič, Andrej; Drofenik, Miha

    2005-03-01

    Magnetic maghemite nanoparticles with a narrow size distribution were prepared in water-CTAB-hexanol-butanol microemulsions. The particle size was controlled with the composition of the microemulsion (water-to-CTAB ratio) and the temperature during synthesis. The saturation magnetization of the nanoparticles depended mainly on their size, ranging from 22 emu/g for a particle size of 3.4 nm to 64 emu/g for a size of 15.3 nm.

  17. “Single-” and “multi-core” FePt nanoparticles: from controlled synthesis via zwitterionic and silica bio-functionalization to MRI applications

    Energy Technology Data Exchange (ETDEWEB)

    Kostevšek, Nina, E-mail: nina.kostevsek@ijs.si; Šturm, Sašo [Jožef Stefan Institute, Department for Nanostructured Materials (Slovenia); Serša, Igor; Sepe, Ana [Jožef Stefan Institute, Department for Condensed Matter Physics (Slovenia); Bloemen, Maarten; Verbiest, Thierry [KU Leuven, Department of Chemistry (Belgium); Kobe, Spomenka; Žužek Rožman, Kristina [Jožef Stefan Institute, Department for Nanostructured Materials (Slovenia)

    2015-12-15

    The value of the magnetization has a strong influence on the performance of nanoparticles that act as the contrast agent material for MRI. In this article, we describe processing routes for the synthesis of FePt nanoparticles of different sizes, which, as a result, exhibit different magnetization values. “Single-core” FePt nanoparticles of different sizes (3–15 nm) were prepared via one-step or two-step synthesis, with the latter exhibiting twice the magnetization (m{sub (1.5T)} = 14.5 emu/g) of the nanoparticles formed via the one-step synthesis (m{sub (1.5T)} < 8 emu/g). Furthermore, we propose the synthesis of “multi-core” FePt nanoparticles by changing the ratio between the two surfactants (oleylamine and oleic acid). The step from smaller “single-core” FePt nanoparticles towards the larger, “multi-core” FePt nanoparticles (>20 nm) leads to an increase in the magnetization m{sub (1.5T)} from 8 to 19.5 emu/g, without exceeding the superparamagnetic limit. Stable water suspensions were prepared using two different approaches: (a) functionalization with a biocompatible, zwitterionic, catechol ligand, which was used on the FePt nanoparticles for the first time, and (b) coating with SiO{sub 2} shells of various thicknesses. These FePt-based nanostructures, the catechol- and SiO{sub 2}-coated “single-core” and “multi-core” FePt nanoparticles, were investigated in terms of the relaxation rates. The higher r{sub 2} values obtained for the “multi-core” FePt nanoparticles compared to that for the “single-core” ones indicate the superiority of the “multi-core” FePt nanoparticles as T{sub 2} contrast agents. Furthermore, it was shown that the SiO{sub 2} coating reduces the r{sub 1} and r{sub 2} relaxation values for both the “single-core” and “multi-core” FePt nanoparticles. The high r{sub 2}/r{sub 1} ratios obtained in our study put FePt nanoparticles near the top of the list of candidate materials for use in MRI

  18. Plant-Mediated Synthesis of Silver Nanoparticles: Their Characteristic Properties and Therapeutic Applications

    Science.gov (United States)

    Chung, Ill-Min; Park, Inmyoung; Seung-Hyun, Kim; Thiruvengadam, Muthu; Rajakumar, Govindasamy

    2016-01-01

    Interest in "green nanotechnology" in nanoparticle biosynthesis is growing among researchers. Nanotechnologies, due to their physicochemical and biological properties, have applications in diverse fields, including drug delivery, sensors, optoelectronics, and magnetic devices. This review focuses on the green synthesis of silver nanoparticles (AgNPs) using plant sources. Green synthesis of nanoparticles is an eco-friendly approach, which should be further explored for the potential of different plants to synthesize nanoparticles. The sizes of AgNPs are in the range of 1 to 100 nm. Characterization of synthesized nanoparticles is accomplished through UV spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and scanning electron microscopy. AgNPs have great potential to act as antimicrobial agents. The green synthesis of AgNPs can be efficiently applied for future engineering and medical concerns. Different types of cancers can be treated and/or controlled by phytonanotechnology. The present review provides a comprehensive survey of plant-mediated synthesis of AgNPs with specific focus on their applications, e.g., antimicrobial, antioxidant, and anticancer activities.

  19. Plant-Mediated Synthesis of Silver Nanoparticles: Their Characteristic Properties and Therapeutic Applications.

    Science.gov (United States)

    Chung, Ill-Min; Park, Inmyoung; Seung-Hyun, Kim; Thiruvengadam, Muthu; Rajakumar, Govindasamy

    2016-12-01

    Interest in "green nanotechnology" in nanoparticle biosynthesis is growing among researchers. Nanotechnologies, due to their physicochemical and biological properties, have applications in diverse fields, including drug delivery, sensors, optoelectronics, and magnetic devices. This review focuses on the green synthesis of silver nanoparticles (AgNPs) using plant sources. Green synthesis of nanoparticles is an eco-friendly approach, which should be further explored for the potential of different plants to synthesize nanoparticles. The sizes of AgNPs are in the range of 1 to 100 nm. Characterization of synthesized nanoparticles is accomplished through UV spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and scanning electron microscopy. AgNPs have great potential to act as antimicrobial agents. The green synthesis of AgNPs can be efficiently applied for future engineering and medical concerns. Different types of cancers can be treated and/or controlled by phytonanotechnology. The present review provides a comprehensive survey of plant-mediated synthesis of AgNPs with specific focus on their applications, e.g., antimicrobial, antioxidant, and anticancer activities. PMID:26821160

  20. Synthesis, characterization, and application of surface-functionalized ordered mesoporous nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Po-Wen

    2009-12-15

    The dissertation begins with Chapter 1, which is a general introduction of the fundamental synthesis of mesoporous silica materials, the selective functionlization of mesoporous silica materials, and the synthesis of nanostructured porous materials via nanocasting. In Chapter 2, the thermo-responsive polymer coated mesoporous silica nanoparticles (MSN) was synthesized via surface-initated polymerization and exhibited unique partition activities in a biphasic solution with the thermally induced change. In Chapter 3, the monodispersed spherical MSN with different mesoporous structure (MCM-48) was developed and employed as a template for the synthesis of mesoporous carbon nanoparticles (MCN) via nanocasting. MCN was demonstrated for the delivery of membrane impermeable chemical agents inside the cells. The cellular uptake efficiency and biocompabtibility of MCN with human cervical cancer cells were also investigated. In addition to the biocompabtibility of MCN, MCN was demonstrated to support Rh-Mn nanoparticles for catalytic reaction in Chapter 4. Owing to the unique mesoporosity, Rh-Mn nanoparticles can be well distributed inside the mesoporous structure and exhibited interesting catalytic performance on CO hydrogenation. In Chapter 5, the synthesis route of the aforementioned MCM-48 MSN was discussed and investigated in details and other metal oxide nanoparticles were also developed via nanocasting by using MCM-48 MSN as a template. At last, there is a general conclusion summarized in Chapter 6.

  1. Herbal Plant Synthesis of Antibacterial Silver Nanoparticles by Solanum trilobatum and Its Characterization

    Directory of Open Access Journals (Sweden)

    M. Vanaja

    2014-01-01

    Full Text Available Green synthesis method of nanomaterials is rapidly growing in the nanotechnology field; it replaces the use of toxic chemicals and time consumption. In this present investigation we report the green synthesis of silver nanoparticles (AgNPs by using the leaf extract of medicinally valuable plant Solanum trilobatum. The influence of physical and chemical parameters on the silver nanoparticle fabrication such as incubation time, silver nitrate concentration, pH, and temperature is also studied in this present context. The green synthesized silver nanoparticles were characterized by UV-vis spectroscopy, X-ray diffraction (XRD, scanning electron microscope (SEM, energy dispersive X-ray (EDX, and transmission electron microscope (TEM. The SEM and TEM confirm the synthesis of spherical shape of nanocrystalline particles with the size range of 2–10 nm. FTIR reveals that the carboxyl and amine groups may be involved in the reduction of silver ions to silver nanoparticles. Antibacterial activity of synthesized silver nanoparticles was done by agar well diffusion method against different pathogenic bacteria. The green synthesized silver nanoparticles can be used in the field of medicine, due to their high antibacterial activity.

  2. The Synthesis, Characterization and Catalytic Reaction Studies of Monodisperse Platinum Nanoparticles in Mesoporous Oxide Materials

    Energy Technology Data Exchange (ETDEWEB)

    Rioux, Robert M. [Univ. of California, Berkeley, CA (United States)

    2006-01-01

    A catalyst design program was implemented in which Pt nanoparticles, either of monodisperse size and/or shape were synthesized, characterized and studied in a number of hydrocarbon conversion reactions. The novel preparation of these materials enables exquisite control over their physical and chemical properties that could be controlled (and therefore rationally tuned) during synthesis. The ability to synthesize rather than prepare catalysts followed by thorough characterization enable accurate structure-function relationships to be elucidated. This thesis emphasizes all three aspects of catalyst design: synthesis, characterization and reactivity studies. The precise control of metal nanoparticle size, surface structure and composition may enable the development of highly active and selective heterogeneous catalysts.

  3. A Facile Solvothermal Synthesis of Octahedral Fe3O4 Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ooi, Frances; DuChene, Joseph S.; Qiu, Jianqing; Graham, Jeremy O.; Engelhard, Mark H.; Cao, Guixin; Gai, Zheng; Wei, Wei

    2015-06-01

    Magnetic nanoparticles are of great technological interest because they promise numerous potential opportunities in biomedicine and data storage. Although intriguing, these applications require exquisite control over nanostructure morphology in order to appropriately harness their magnetic properties. Most synthesis strategies reported to date are unable to routinely produce anisotropic Fe3O4 nanostructures with appropriate sizes to enable integration into biological systems. Here, we report a simple solvothermal synthesis for obtaining octahedral Fe3O4 nanoparticles with suitable sizes for cellular internalization. Furthermore, these ferromagnetic Fe3O4 octahedrons exhibit substantial saturation magnetization with minimal remanence, suggesting their potential applicability for a host of biomedical applications.

  4. Synthesis of carbon nanoparticles from commercially available liquified petroleum gas

    Science.gov (United States)

    Nandiyanto, A. B. D.; Fadhlulloh, M. A.; Rahman, T.; Mudzakir, A.

    2016-04-01

    The aim of this study was to synthesize carbon nanoparticles (CNPs) from commercially available liquefied petroleum gas (LPG). In the research procedure, LPG was reacted with air to construct CNPs. To confirm the successful synthesis of CNPs, we conducted several sample analyses: Gas Chromatography-Mass Spectrometry (GC-MS), Transmission Electron Microscope (TEM), X-ray Diffraction (XRD), and Infrared Spectra (FTIR). We also varied LPG and oxygen mole ratios at 0.8; 2.4; 4.8; and 7.2. The GC-MS results indicated the composition of LPG was propane (58.90%), isobutane (18.35%), butane (22.26%), and butane, 2-methyl (0.48%). The TEM results showed that the particles were spheres with sizes of between 25 and 35 nm. The sizes of particles were controllable, depending on the mole ratio. The XRD results showed mole ratios of LPG and oxygen of 0.80 and 2.40 were natural graphite, whereas the mole ratios of 4.80 and 7.20 were hexagonal graphite. FT-IR results showed CNPs have absorption peaks at wave number (i) 752 (C-H bend sp2); (ii) 835 (C=C); (iii) 1274 (C-O-C vibration); (iv) 1400 and 1600 (C-C stretch aromatic); (v) 2800 (C-H sp2); (vi) 2900 (CH sp3); (vii) 3100 (C-H aromatic); and (viii) 3400 cm-1 (O-H). From the FTIR analysis results, the sample contained allotrope graphite due to detection of peaks at 1400 and 1600 cm-1 (C-C stretch aromatic) and 3100 cm-1 (C-H aromatic).

  5. Controllable synthesis of silver nanoparticles using Neem leaves and their antimicrobial activity

    Directory of Open Access Journals (Sweden)

    Aparajita Verma

    2016-01-01

    Full Text Available Silver nanoparticles (AgNPs were synthesized using aqueous extract of Neem (Azadirachta indica leaves and silver salt. XRD, SEM, FTIR, optical absorption and photoluminescence (PL were measured and analysed. The synthesized AgNPs exhibits lowest energy absorption band at 400 nm. The effects of various parameters i.e., extract concentration, reaction pH, reactants ratio, temperature and interaction time on the synthesis of AgNPs were studied. It was found that the formation of AgNPs enhanced with time at higher temperature and alkaline pH. The AgNPs formed were found to have enhanced antimicrobial properties and showed zone of inhibition against isolated bacteria (Escherichia coli from garden soil sample. Based on the results obtained, it can be concluded that the resources obtained from plants can be efficiently used in the production of AgNPs and could be utilized in various fields such as biomedical, nanotechnology etc.

  6. Green synthesis and characterization of alginate nanoparticles and its role as a biosorbent for Cr(VI) ions

    Science.gov (United States)

    Geetha, P.; Latha, M. S.; Pillai, Saumya S.; Deepa, B.; Santhosh Kumar, K.; Koshy, Mathew

    2016-02-01

    Green synthesis of nanoparticles has attained considerable attention in recent years because of its myriad of applications including drug delivery, tissue engineering and water purification. In the present study, alginate nanoparticles stabilized by honey were prepared by cross-linking aqueous solution of alginate with calcium ions. Honey mediated synthesis has been reported earlier for the production of metal nanoparticles. However no literature is available on the use of this technique for polymeric nanoparticles. Highly stable nanoparticles of 10-100 nm size were generated by this technique. The synthesised nanoparticles were characterized by transmission electron microscopy, scanning electron microscopy, atomic force microscopy, dynamic light scattering and Fourier transform infrared spectroscopic techniques. Potential of using these nanoparticles for heavy metal removal was studied by using Cr(VI) from aqueous solution, where a maximum removal efficiency of 93.5% was obtained. This method was also successfully employed for the production of other polymeric nanoparticles like casein, chitosan and albumin.

  7. ANALYSIS-BASED SPARSE RECONSTRUCTION WITH SYNTHESIS-BASED SOLVERS

    OpenAIRE

    Cleju, Nicolae; Jafari, Maria,; Plumbley, Mark D.

    2012-01-01

    Analysis based reconstruction has recently been introduced as an alternative to the well-known synthesis sparsity model used in a variety of signal processing areas. In this paper we convert the analysis exact-sparse reconstruction problem to an equivalent synthesis recovery problem with a set of additional constraints. We are therefore able to use existing synthesis-based algorithms for analysis-based exact-sparse recovery. We call this the Analysis-By-Synthesis (ABS) approach. We evaluate o...

  8. Synthesis and characterization of Gold and Silver nano-particles using different leaf extracts namely Catharanthus roseus, Datura metel and Azadirachta indica and Estimation of antimicrobial activity of silver nano-particles using disc diffusion method

    OpenAIRE

    Sarbjeet Singh Gujral

    2014-01-01

    Objective: synthesis of gold and silver nano-particles using leaf extracts of Catharanthus roseus, Datura metel and Azadirachta indica and Estimation of antimicrobial activity of silver nano-particles using disc diffusion method. Method: Green approach has been utilized for the synthesis of gold and silver nano-particles. Different aqueous plant extracts has been prepared which was then utilized for the biosynthesis of gold and silver nano-particles. Estimation for the synthesis of nano-parti...

  9. Gold nanoparticles with cyclic phenylazomethines: one-pot synthesis and metal ion sensing.

    Science.gov (United States)

    Shomura, Ryo; Chung, Keum Jee; Iwai, Hideo; Higuchi, Masayoshi

    2011-07-01

    New gold nanoparticles covered with cyclic phenylazomethine (CPA) were obtained by a one-pot synthesis. It is confirmed by XPS that imines of CPA in the nanoparticles (Au-CPA) are partially reduced to amines. The amine part of CPA in Au-CPA is attached to the surfaces of gold nanoparticles, and the imine part works as a redox-active site. A glassy carbon electrode modified with Au-CPA was revealed to work as an electrochemical probe for metal ion sensing.

  10. Green synthesis of palladium nanoparticles using broth of Cinnamomum camphora leaf

    Energy Technology Data Exchange (ETDEWEB)

    Yang Xin; Li Qingbiao, E-mail: kelqb@xmu.edu.cn; Wang Huixuan; Huang Jiale; Lin Liqin; Wang Wenta; Sun Daohua; Su Yuanbo; Opiyo, James Berya; Hong Luwei; Wang Yuanpeng; He Ning; Jia Lishan [College of Chemistry and Chemical Engineering, Xiamen University, Department of Chemical and Biochemical Engineering (China)

    2010-06-15

    The development of dependable, environmentally benign processes for the synthesis of nanoscale materials is an important aspect of nanotechnology. In the present study, we report one-pot biogenic fabrication of palladium nanoparticles by a simple procedure using broth of Cinnamomum camphora leaf without extra surfactant, capping agent, and/or template. The mean size of palladium nanoparticles, ranging from 3.2 to 6.0 nm, could be facilely controlled by merely varying the initial concentration of the palladium ions. The polyols components and the heterocyclic components were believed to be responsible for the reduction of palladium ions and the stabilization of palladium nanoparticles, respectively.

  11. Radio-synthesized protein-based nanoparticles for biomedical purposes

    International Nuclear Information System (INIS)

    Protein-crosslinking whether done by enzymatic or chemically induced pathways increases the overall stability of proteins. In the continuous search for alternative routes for protein stabilization we report a novel technique – radio-induced synthesis of protein nanoparticles – to achieve size controlled particles with preserved bioactivity. Papain was used as model enzyme and the samples were irradiated at 10 kGy in a gammacell irradiator in phosphate buffer (pH=7.0) and additives such as ethanol (0–40%) and sodium chloride (0–25%). The structural rearrangement caused by irradiation under defined conditions led to an increase in papain particle size as a function of the additive and its concentration. These changes occur due to intermolecular bindings, of covalent nature, possibly involving the aromatic amino acids. Ethanol held major effects over papain particle size and particle size distribution if compared to sodium chloride. The particles presented relative retained bioactivity and the physic-chemical characterization revealed similar fluorescence spectra indicating preserved conformation. Differences in fluorescence units were observed according to the additive and its concentration, as a result of protein content changes. Therefore, under optimized conditions, the developed technique may be applied for enzyme nanoparticles formation of controllable size and preserved bioactivity. Highlights: • Novel technique for the development of protein nanoparticles using γ-irradiation. • Size control of papain particles with preserved conformation and bioactivity. • Alternative method for controlled protein crosslinking. • Bioactive protein nanoparticles of biotechnological and clinical interest. • Protein-based drug carrier potential of biotechnological and clinical interest

  12. Extracellular synthesis of silver nanoparticles by novel Pseudomonas veronii AS41G inhabiting Annona squamosa L. and their bactericidal activity

    Science.gov (United States)

    Baker, Syed; Mohan Kumar, K.; Santosh, P.; Rakshith, D.; Satish, S.

    2015-02-01

    In present investigation extracellular synthesis of silver nanoparticles were synthesized using cell free supernatant of Pseudomonas veronii AS41G isolated from Annona squamosa L. The bacterium significantly reduced silver nitrate to generate silver nanoparticles which was characterized with hyphenated techniques. Synthesis of silver nanoparticles preliminary confirmed by UV-Visible spectrophotometry with the intense peak at 410 nm, Further FTIR analysis revealed the possible role of biomolecules in the supernatant responsible for mediating the nanoparticles formation. The XRD spectra exhibited the characteristic Bragg peaks of 1 0 0, 1 1 1, 2 0 0, and 2 2 0 facets of the face centred cubic symmetry of nanoparticles suggesting that these nanoparticles were crystalline in nature. TEM microgram showed polydispersity of nanoparticles with size ranging from 5 to 50 nm. Synthesized silver nanoparticles showed antibacterial activity against human and environmental pathogens including MRSA. The study enlightens the role of biosynthesized silver nanoparticles as an emerging alternative for drug resistant microorganisms. The obtained results are promising enough to pave the environmentally benign nanoparticle synthesis processes without use of any toxic chemicals and also envision the emerging role of endophytes towards synthesis of nanoparticles. With scanty reports available on P.veronii species, a new role has been reported in this study which will be very valuable for future researchers working on it.

  13. Gold Nanoparticles: Synthesis, Stability Test, and Application for the Rice Growth

    Directory of Open Access Journals (Sweden)

    Aiwu Wang

    2014-01-01

    Full Text Available In today’s science, with the use of nanotechnology, nanomaterials, which behave very differently from the bulk solid, can be made. One of the capable uses of nanomaterials is bioapplications which make good use of the specific properties of nanoparticles. However, since the nanoparticles will be used both in-vivo and in-vitro, their stability is an important issue to the scientists, concern. In this dissertation, we are going to test the stability of gold nanoparticles in a number of media including the biocompatible medium and their behaviors will be illustrated in terms of optical properties change and aggregation degree. Herein, we report the synthesis of gold nanoparticles of different shapes and applications for the rice growth with significant difference. The gold nanoparticles can inhibit the elongation of rice root without inhibiting the germination of rice seeds.

  14. Quantum Mechanics of Insitu Synthesis of Inorganic Nanoparticles with in Anionic Microgels

    CERN Document Server

    Baig, Mirza Wasif

    2013-01-01

    In this work, we discuss the quantum mechanics of many-body systems i.e. hybrid microgel consisting of negatively charged anionic microgels possessing thick sheath of water molecules solvating its protruding anionic moieties and nanoparticle captivated with in it. Thermodynamic feasibility of synthesis of particular nanoparticle with in the microgel is dependent upon the magnitude of interaction between nanoparticle, water molecules and microgel relative to sum of magnitude of self-interaction between counterions and interaction between counterions and microgel. Nanoparticles synthesized with in the microgels have thick electronic cloud that oscillates under the influence of net interaction potential of charged anionic moieties and solvent water molecules. Hamiltonian describing energy of oscillating electronic cloud wrapped around nanoparticle is mathematically derived to be equal to product of integral of electron density and its position vector overall space multiplied with net electric force acting on the...

  15. Synthesis of noble metal nanoparticles and their superstructures; Darstellung von Edelmetallnanopartikeln und deren Ueberstrukturen

    Energy Technology Data Exchange (ETDEWEB)

    Bigall, Nadja-Carola

    2009-08-18

    A modified synthesis procedure for citrate-stabilized gold nanoparticles in aqueous solution is transferred under application of equal concentrations to the systems silver, platinum, and palladium. The nanoparticles are analyzed by means of absorption spectroscopy and electron microscopy. Ordered superstructures of the noble-metal nanoparticles can be synthesized by infiltration of templates of block-copolymer films with aqueous nanoparticle solution. In dependence on the pre-treatment of the polymer films either two-dimensional periodical arrangements with a periodicity of less than 30 nm or fingerprint-like arrangements with a groove distance in the same order of magnitude. By removal of the polymer one- respectively two-dimensional arrangements of platinum nanowires respectively nanoparticles on a silicon waver arise.

  16. Optimization for rapid synthesis of silver nanoparticles and its effect on phytopathogenic fungi

    Science.gov (United States)

    Krishnaraj, C.; Ramachandran, R.; Mohan, K.; Kalaichelvan, P. T.

    In this present study, silver nanoparticles were synthesized by green chemistry approach using Acalypha indica leaf extract as reducing agents. The reaction medium employed in the synthesis process was optimized to attain better yield, controlled size and stability. Further, the biosynthesized silver nanoparticles were conformed through UV-vis spectrum, XRD and HR-TEM analyses. Different concentration of silver nanoparticles were tested to know the inhibitory effect of fungal plant pathogens namely Alternaria alternata, Sclerotinia sclerotiorum, Macrophomina phaseolina, Rhizoctonia solani, Botrytis cinerea and Curvularia lunata. Interestingly, 15 mg concentration of silver nanoparticles showed excellent inhibitory activity against all the tested pathogens. Thus, the obtained results clearly suggest that silver nanoparticles may have important applications in controlling various plant diseases caused by fungi.

  17. Synthesis of aluminium nanoparticles by arc evaporation of an aluminium cathode surface

    Indian Academy of Sciences (India)

    M Gazanfari; M Karimzadeh; S Ghorbani; M R Sadeghi; G Azizi; H Karimi; N Fattahi; Z Karimzadeh

    2014-06-01

    Aluminium nanoparticles (Al Nps) are synthesized using arc discharge method by applying direct current between aluminium electrodes in liquid environment without any use of vacuum equipment, heat exchangers, high temperatures furnaces and inert gases. After synthesis of Al Nps, in situ coating process on the nanoparticles was performed immediately. The effects of media on the yield and morphology of aluminium nanoparticles were investigated. Analysis result of the samples indicated that particle size was less than 30 nm, when 120 A/cm2 arc current was used. In addition, coating agent can affect arc velocity, arc stability, morphology and composition of the nanoparticles. Resultant nanoparticles were identified using X-ray powder diffraction (XRD), also their surface morphology was studied by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) and finally the accuracy of coating was assessed with infrared (IR) spectroscopy.

  18. Bioactive Glass Nanoparticles: From Synthesis to Materials Design for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    Charlotte Vichery

    2016-04-01

    Full Text Available Thanks to their high biocompatibility and bioactivity, bioactive glasses are very promising materials for soft and hard tissue repair and engineering. Because bioactivity and specific surface area intrinsically linked, the last decade has seen a focus on the development of highly porous and/or nano-sized materials. This review emphasizes the synthesis of bioactive glass nanoparticles and materials design strategies. The first part comprehensively covers mainly soft chemistry processes, which aim to obtain dispersible and monodispersed nanoparticles. The second part discusses the use of bioactive glass nanoparticles for medical applications, highlighting the design of materials. Mesoporous nanoparticles for drug delivery, injectable systems and scaffolds consisting of bioactive glass nanoparticles dispersed in a polymer, implant coatings and particle dispersions will be presented.

  19. Facile Synthesis of Biocompatible Fluorescent Nanoparticles for Cellular Imaging and Targeted Detection of Cancer Cells.

    Science.gov (United States)

    Tang, Fu; Wang, Chun; Wang, Xiaoyu; Li, Lidong

    2015-11-18

    In this work, we report the facile synthesis of functional core-shell structured nanoparticles with fluorescence enhancement, which show specific targeting of cancer cells. Biopolymer poly-l-lysine was used to coat the silver core with various shell thicknesses. Then, the nanoparticles were functionalized with folic acid as a targeting agent for folic acid receptor. The metal-enhanced fluorescence effect was observed when the fluorophore (5-(and-6)-carboxyfluorescein-succinimidyl ester) was conjugated to the modified nanoparticle surface. Cellular imaging assay of the nanoparticles in folic acid receptor-positive cancer cells showed their excellent biocompatibility and selectivity. The as-prepared functional nanoparticles demonstrate the efficiency of the metal-enhanced fluorescence effect and provide an alternative approach for the cellular imaging and targeting of cancer cells.

  20. PHYTOCHEMICAL SCREENING AND ANTIBACTERIAL ACTIVITY FROM NERIUM OLEANDER AND EVALUVATE THEIR PLANT MEDIATED NANOPARTICLE SYNTHESIS

    Directory of Open Access Journals (Sweden)

    R.S. Suganya

    2012-05-01

    Full Text Available Phytochemical and antibacterial activity of essential oils obtained from Nerium oleander leaf with the help of three different extracts like ethanol, Methanol, and acetone. In this aqueous leaf extracts confirms the presence of various phytochemicals. To evaluate the antibacterial activities of these aqueous extracts were determined by disc diffusion method. From these three extracts methanol shows strong antibacterial effect on Klebsiella, Pseudomonas, Alkaligenes except Acinetobacter. None of the leaf extracts show no more activity in Acinetobacter. Biologically synthesized nanoparticles have been widely used in the field of medicine. Shade dried leaves of Nerium oleander was used for the synthesis of silver nanoparticles. UV- Visible spectroscopy studies were carried out to assess the formation of Ag nanoparticles. Scanning electron microscope (SEM was used to characterize the Ag nanoparticle. To compare the antimicrobial activity of silver nanoparticles with the different leaf extracts.