WorldWideScience

Sample records for carbon nanoparticles synthesis

  1. SYNTHESIS AND CHARACTERIZATION OF COPPER CARBONATE NANOPARTICLES

    OpenAIRE

    R.Hepzi Pramila Devamani; Sabeena, M.

    2014-01-01

    Copper carbonate nanoparticles were synthesized via chemical co-precipitation method from copper sulphate and sodium carbonate. The formed nanoparticle is characterized by powder x-ray diffraction, scanning electron microscopy, ultra-violet spectroscopy and fourier transform infrared spectroscopy, confirmed the preferential growth of copper carbonate nanoparticles that width is 90.55nm. The SEM image shows the synthesized copper carbonate show well crystallized particles with ...

  2. SYNTHESIS AND CHARACTERIZATION OF COPPER CARBONATE NANOPARTICLES

    Directory of Open Access Journals (Sweden)

    R.Hepzi Pramila Devamani

    2014-04-01

    Full Text Available Copper carbonate nanoparticles were synthesized via chemical co-precipitation method from copper sulphate and sodium carbonate. The formed nanoparticle is characterized by powder x-ray diffraction, scanning electron microscopy, ultra-violet spectroscopy and fourier transform infrared spectroscopy, confirmed the preferential growth of copper carbonate nanoparticles that width is 90.55nm. The SEM image shows the synthesized copper carbonate show well crystallized particles with spherical morphology. The FTIR spectrum is used to study the stretching and bending frequencies of molecular functional groups in the sample. From UV spectrum, the band gap of copper carbonate nanoparticles is found to be 3.4eV.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. Camphor-mediated synthesis of carbon nanoparticles, graphitic shell encapsulated carbon nanocubes and carbon dots for bioimaging

    OpenAIRE

    Goldie Oza; Ravichandran, M.; Victor-Ishrayelu Merupo; Sachin Shinde; Ashmi Mewada; Jose Tapia Ramirez; Velumani, S.; Madhuri Sharon; Maheshwar Sharon

    2016-01-01

    A green method for an efficient synthesis of water-soluble carbon nanoparticles (CNPs), graphitic shell encapsulated carbon nanocubes (CNCs), Carbon dots (CDs) using Camphor (Cinnamomum camphora) is demonstrated. Here, we describe a competent molecular fusion and fission route for step-wise synthesis of CDs. Camphor on acidification and carbonization forms CNPs, which on alkaline hydrolysis form CNCs that are encapsulated by thick graphitic layers and on further reduction by sodium borohydrid...

  8. 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.

  9. Synthesis and characterization of carbon nanotubes decorated with platinum nanoparticles

    Directory of Open Access Journals (Sweden)

    L.A. Dobrzański

    2010-04-01

    Full Text Available Purpose: In presented work results of synthesis of carbon nanotubes decorated with platinum nanoparticles by organic colloidal process as an example of direct formation of nanoparticles onto CNTs are reported.Design/methodology/approach: CNT were grown by chemical vapour deposition (CVD by the catalytic decomposition of CO. To improve metal deposition onto CNTs the purification procedure with a mixture of concentrated HNO3–H2SO4 and H2O2 reduction reagent was applied. CNT–nanocrystal composite was fabricated by direct deposition of nanoparticles onto the surface of CNTs. Chemical composition and crystallographic structure of the obtained Pt/CNT composites were confirmed by energy dispersive X-ray spectroscopy (EDS and by X-ray diffraction (XRD measurements, while transmission (TEM and scanning electron microscopy (SEM were used for characterization of the morphology of composite as well as the distribution of nanocrystals on the CNTs surfaces.Findings: High efficiency of proposed method was confirmed as well as possibility of the coating of Pt nanoparticles onto CNTs, without aggregation of these particles.Research limitations/implications: Many others noble metals such as palladium, platinum, gold and iridium can be used for deposition on the CNTs using described procedure.Originality/value: Obtained material can be employed in constructing various electrochemical sensors. As a result of increasing of the surface area of Pt caused by the reduction of the size of used particles, fabricated sensor may be characterized by higher sensitivity.

  10. 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...

  11. 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.

  12. One step synthesis of Al/N co-doped carbon nanoparticles with enhanced photoluminescence

    International Nuclear Information System (INIS)

    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(NO3)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

  13. 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.

  14. 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).

  15. Camphor-mediated synthesis of carbon nanoparticles, graphitic shell encapsulated carbon nanocubes and carbon dots for bioimaging

    Science.gov (United States)

    Oza, Goldie; Ravichandran, M.; Merupo, Victor-Ishrayelu; Shinde, Sachin; Mewada, Ashmi; Ramirez, Jose Tapia; Velumani, S.; Sharon, Madhuri; Sharon, Maheshwar

    2016-02-01

    A green method for an efficient synthesis of water-soluble carbon nanoparticles (CNPs), graphitic shell encapsulated carbon nanocubes (CNCs), Carbon dots (CDs) using Camphor (Cinnamomum camphora) is demonstrated. Here, we describe a competent molecular fusion and fission route for step-wise synthesis of CDs. Camphor on acidification and carbonization forms CNPs, which on alkaline hydrolysis form CNCs that are encapsulated by thick graphitic layers and on further reduction by sodium borohydride yielded CDs. Though excitation wavelength dependent photoluminescence is observed in all the three carbon nanostructures, CDs possess enhanced photoluminescent properties due to more defective carbonaceous structures. The surface hydroxyl and carboxyl functional groups make them water soluble in nature. They possess excellent photostability, higher quantum yield, increased absorption, decreased cytotoxicity and hence can be utilized as a proficient bio imaging agent.

  16. Camphor-mediated synthesis of carbon nanoparticles, graphitic shell encapsulated carbon nanocubes and carbon dots for bioimaging.

    Science.gov (United States)

    Oza, Goldie; Ravichandran, M; Merupo, Victor-Ishrayelu; Shinde, Sachin; Mewada, Ashmi; Ramirez, Jose Tapia; Velumani, S; Sharon, Madhuri; Sharon, Maheshwar

    2016-01-01

    A green method for an efficient synthesis of water-soluble carbon nanoparticles (CNPs), graphitic shell encapsulated carbon nanocubes (CNCs), Carbon dots (CDs) using Camphor (Cinnamomum camphora) is demonstrated. Here, we describe a competent molecular fusion and fission route for step-wise synthesis of CDs. Camphor on acidification and carbonization forms CNPs, which on alkaline hydrolysis form CNCs that are encapsulated by thick graphitic layers and on further reduction by sodium borohydride yielded CDs. Though excitation wavelength dependent photoluminescence is observed in all the three carbon nanostructures, CDs possess enhanced photoluminescent properties due to more defective carbonaceous structures. The surface hydroxyl and carboxyl functional groups make them water soluble in nature. They possess excellent photostability, higher quantum yield, increased absorption, decreased cytotoxicity and hence can be utilized as a proficient bio imaging agent. PMID:26905737

  17. Facile Instep Synthesis of Palladium Nanoparticle/Carbon@Carbon Nanotube Composites for Electrooxidation of Xylitol.

    Science.gov (United States)

    Kannan, Ramanujam; Kim, Ae Rhan; Nahm, Kee Suk; Yoo, Dong Jin

    2016-03-01

    The development of a facile, instep, and eco-friendly synthesis method of mono-dispersed low quantity palladium nanoparticle/carbon@functionllized carbon nanotube composite (Pd@C-f-CNT)electrocatalytic material was developed for use in the electrooxidation of xylitol. The prepared nanocatalyst was analyzed by powder X-ray diffraction analysis, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning and transmission electron microscopy. The electrocatalytic studies were performed using voltammetric methods. Formation of Pd NPs was observed within 2 min. The microscopic analysis showed 5- to 10-nm-sized Pd NPs that uniformly covered the CNT. The instep-formed carbon helped to improve the electrocatalytic activity of the catalyst. Our proposed method provides new insight for the development of highly efficient metal NPs/CNT nanocatalyst for direct alcohol fuel cell applications. PMID:27455674

  18. One-step synthesis of fluorescent carbon nanoparticles for degradation of naphthol green under visible light

    International Nuclear Information System (INIS)

    A novel solvothermal approach to synthesize fluorescent carbon nanoparticles (CNPs) was developed by using citric acid and ammonium oxalateas as the carbon source, glycol as the solvent. The solution of the as-prepared CNPs emitted strong blue fluorescence under UV 365 nm, and the particles were well- dispersed with an average diameter of about 30–40 nm. The solution of the obtained CNPs was applied to photocatalytic degradation of naphthol green, and the decolorization rate is over 91% when the reaction time reaches more than 5 h under visible light in the presence of hydrogen peroxide. - Highlights: • A one-step synthesis of carbon nanoparticles method was developed. • The citric acid and ammoniumoxalate were used as carbon source for the first time. • The photocatalytic activity of carbon nanoparticles under visible light was evaluated

  19. Synthesis and Characterization of Carbon Nanotubes Decorated with Gold Nanoparticles

    International Nuclear Information System (INIS)

    In presented work we report results of simple and viable method for producing Au/CNT composites. Chemical composition and crystallographic structure of the Au/CNT composites was confirmed by X-ray diffraction measurements, while transmission and scanning electron microscopy were used to characterize the morphology of nanocrystals as well as the distribution of nanocrystals in the composite. The obtained particles with relatively small diameter (less than 9 nm) were found to be spatially well dispersed on the carbon nanotubes. The density of attached Au-nanoparticles is not sufficient, and cannot be improved by simple increasing gold loading. (authors)

  20. Multiple-diffusion flame synthesis of pure anatase and carbon-coated titanium dioxide nanoparticles

    KAUST Repository

    Memon, Nasir

    2013-09-01

    A multi-element diffusion flame burner (MEDB) is useful in the study of flame synthesis of nanomaterials. Here, the growth of pure anatase and carbon-coated titanium dioxide (TiO2) using an MEDB is demonstrated. Hydrogen (H2), oxygen (O2), and argon (Ar) are utilized to establish the flame, whereas titanium tetraisopropoxide is used as the precursor for TiO2. The nanoparticles are characterized using high-resolution transmission electron microscopy, with elemental mapping (of C, O, and Ti), X-ray diffraction, Raman spectroscopy, and thermogravimetric analysis. The growth of pure anatase TiO2 nanoparticles occurs when Ar and H2 are used as the precursor carrier gas, while the growth of carbon-coated nanoparticles ensues when Ar and ethylene (C2H4) are used as the precursor carrier gas. A uniform coating of 3-5nm of carbon is observed around TiO2 particles. The growth of highly crystalline TiO2 nanoparticles is dependent on the gas flow rate of the precursor carrier and amorphous particles are observed at high flow rates. Carbon coating occurs only on crystalline nanoparticles, suggesting a possible growth mechanism of carbon-coated TiO2 nanoparticles. © 2013 The Combustion Institute.

  1. Natural reducing agents for electroless nanoparticle deposition: Mild synthesis of metal/carbon nanostructured microspheres

    International Nuclear Information System (INIS)

    Composite materials are of interest because they can potentially combine the properties of their respective components in a manner that is useful for specific applications. Here, we report on the use of coffee as a low-cost, green reductant for the room temperature formation of catalytically active, supported metal nanoparticles. Specifically, we have leveraged the reduction potential of coffee in order to grow Pd and Ag nanoparticles at the surface of porous carbon microspheres synthesized via ultraspray pyrolysis. The metal nanoparticle-on-carbon microsphere composites were characterized using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and thermal gravimetric analysis (TGA). To demonstrate the catalytic activity of Pd/C and Ag/C materials, Suzuki coupling reactions and nitroaromatic reduction reactions were employed, respectively. - Highlights: • Natural reductants were used as green electroless deposition reagents. • Room temperature synthesis of supported Ag and Pd nanoparticles was achieved. • Carbon porous microspheres were used as supports. • Synthesis via natural reductants yielded catalytically active nanoparticles.

  2. Natural reducing agents for electroless nanoparticle deposition: Mild synthesis of metal/carbon nanostructured microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Duffy, Paul [School of Chemistry, University of Dublin Trinity College, College Green, Dublin 2 (Ireland); Reynolds, Lyndsey A.; Sanders, Stephanie E. [Department of Chemistry, Albion College, 611 E. Porter St., Albion, MI 49224 (United States); Metz, Kevin M., E-mail: kmetz@albion.edu [Department of Chemistry, Albion College, 611 E. Porter St., Albion, MI 49224 (United States); Colavita, Paula E., E-mail: colavitp@tcd.ie [School of Chemistry, University of Dublin Trinity College, College Green, Dublin 2 (Ireland); Centre for Research on Adaptive Nanostructures and Nanodevices (CRANN), Trinity College Dublin, Dublin 2 (Ireland)

    2013-06-15

    Composite materials are of interest because they can potentially combine the properties of their respective components in a manner that is useful for specific applications. Here, we report on the use of coffee as a low-cost, green reductant for the room temperature formation of catalytically active, supported metal nanoparticles. Specifically, we have leveraged the reduction potential of coffee in order to grow Pd and Ag nanoparticles at the surface of porous carbon microspheres synthesized via ultraspray pyrolysis. The metal nanoparticle-on-carbon microsphere composites were characterized using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and thermal gravimetric analysis (TGA). To demonstrate the catalytic activity of Pd/C and Ag/C materials, Suzuki coupling reactions and nitroaromatic reduction reactions were employed, respectively. - Highlights: • Natural reductants were used as green electroless deposition reagents. • Room temperature synthesis of supported Ag and Pd nanoparticles was achieved. • Carbon porous microspheres were used as supports. • Synthesis via natural reductants yielded catalytically active nanoparticles.

  3. Macroporous carbon decorated with dendritic platinum nanoparticles: one-step synthesis and electrocatalytic properties

    Science.gov (United States)

    Yu, Xueqing; Zhang, Yufan; Guo, Liping; Wang, Liang

    2014-04-01

    Macroporous carbon (MPC) with high pore accessibility and electrical conductivity is of great interest to the electrochemical platform. The development of a simple and efficient route for the direct synthesis of dendritic platinum nanoparticle (DPN) decorated MPC (DPN/MPC) is an interesting challenge, which is highly valuable for electrocatalytic applications. In this study, we propose a very simple route for the one-step synthesis of DPN/MPC in aqueous solution at room temperature without the need for any kind of seed and surfactant to direct the dendritic growth of Pt nanoparticles, which is performed by simply mixing an aqueous solution of K2PtCl4 with MPC and formic acid. The as-prepared DPN/MPC shows high electrocatalytic activities toward the oxidation of methanol and glucose.

  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...

  5. Synthesis of carbon nanoparticles using one step green approach and their application as mercuric ion sensor

    Energy Technology Data Exchange (ETDEWEB)

    Roshni, V.; Ottoor, Divya, E-mail: divya@chem.unipune.ac.in

    2015-05-15

    Carbon nanoparticles (CNPs) have been evolved as a promising candidate for the metal sensing applications due to their synthesis from naturally occurring and easily available non-toxic molecular precursors by green chemistry. A simple and one step procedure is reported here for the synthesis of CNPs from coconut milk by thermal pyrolysis at a temperature of 120–150 °C for 2–5 min without using any carbonizing or passivating agent. On pyrolysis the coconut oil is separated from the carbon rich residue and the residue when dissolved in water showed blue fluorescence under UV light. The CNPs produced are found to show an emission maximum at 440 nm when excited at 360 nm. Synthesis by green approach makes CNPs a promising substitute for the metal sensing applications. Series of metal ions which have a hazardous impact on the ecological system have been taken for the analysis and it is observed that the fluorescence of CNPs gets remarkably quenched by mercuric ions. Fluorescence quenching was studied using standard Stern–Volmer quenching model. Limit of detection was found to be 16.5 nM Hg{sup 2+} concentration. - Highlights: • Green and economical synthesis of carbon nanoparticles (CNPs) from naturally abundant material. • Coconut milk is used as molecular precursor, which on thermal pyrolysis at 120 °C yielded CNPs. • Highly fluorescent CNPs show an emission maxima of 440 nm when excited at 360 nm. • Application of CNPs for metal ion sensing using fluorescence quenching phenomena. • Hg{sup 2+} is most effectively sensed with a detection limit of 16.5 nM.

  6. Synthesis of carbon nanoparticles using one step green approach and their application as mercuric ion sensor

    International Nuclear Information System (INIS)

    Carbon nanoparticles (CNPs) have been evolved as a promising candidate for the metal sensing applications due to their synthesis from naturally occurring and easily available non-toxic molecular precursors by green chemistry. A simple and one step procedure is reported here for the synthesis of CNPs from coconut milk by thermal pyrolysis at a temperature of 120–150 °C for 2–5 min without using any carbonizing or passivating agent. On pyrolysis the coconut oil is separated from the carbon rich residue and the residue when dissolved in water showed blue fluorescence under UV light. The CNPs produced are found to show an emission maximum at 440 nm when excited at 360 nm. Synthesis by green approach makes CNPs a promising substitute for the metal sensing applications. Series of metal ions which have a hazardous impact on the ecological system have been taken for the analysis and it is observed that the fluorescence of CNPs gets remarkably quenched by mercuric ions. Fluorescence quenching was studied using standard Stern–Volmer quenching model. Limit of detection was found to be 16.5 nM Hg2+ concentration. - Highlights: • Green and economical synthesis of carbon nanoparticles (CNPs) from naturally abundant material. • Coconut milk is used as molecular precursor, which on thermal pyrolysis at 120 °C yielded CNPs. • Highly fluorescent CNPs show an emission maxima of 440 nm when excited at 360 nm. • Application of CNPs for metal ion sensing using fluorescence quenching phenomena. • Hg2+ is most effectively sensed with a detection limit of 16.5 nM

  7. 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

  8. Synthesis of carbon-supported titanium oxynitride nanoparticles as cathode catalyst for polymer electrolyte fuel cells

    International Nuclear Information System (INIS)

    Highlights: • A sol–gel route for the synthesis of rutile TiO2 was modified to synthesize TiOxNy-C. • N atoms were doped into TiOx nanoparticles solely by the heat-treatment under N2 gas. • The N2-treatment produced sites more active toward ORR compared with NH3-treatment. • TiOx doped with a small amount of N atoms are suggested to be responsible for ORR. -- Abstract: For use as the oxygen reduction reaction (ORR) catalyst in polymer electrolyte fuel cell cathodes, carbon-supported titanium oxynitride (TiOxNy-C) nanoparticles with a size of approximately 5 nm or less were synthesized without using NH3 gas. A sol–gel route developed for the synthesis of pure rutile TiO2 nanopowders was modified to prepare the carbon-supported titanium oxide nanoparticles (TiOx-C). For the first time, N atoms were doped into TiOx solely by heating TiOx-C under an inexpensive N2 atmosphere at 873 K for 3 h, which could be due to carbothermal reduction. The TiOx-C powder was also heated under NH3 gas at various temperatures (873–1273 K) and durations (3–30 h). This step resulted in the formation of a TiN phase irrespective of the heating conditions. Both N2- and NH3-treated TiOxNy-C did not crystallize well; however, the former showed a mass activity more than three times larger than that of the latter at 0.74 V versus the standard hydrogen electrode. Thus, titanium oxide nanoparticles doped with a small amount of N atoms are suggested to be responsible for catalyzing ORR in the case of N2-treated TiOxNy-C

  9. Facile synthesis of platinum nanoparticle-containing porous carbons, and their application to amperometric glucose biosensing

    International Nuclear Information System (INIS)

    This study describes the facile synthesis of platinum nanoparticle-containing porous carbons (Pt/C) by carbonization of freeze-dried agarose gels containing potassium tetrachloroplatinate under a nitrogen atmosphere at 800 °C. By adjusting the ratio between agarose and platinate in the freeze-dried gels, the Pt content in the final Pt/C products could be systematically varied from 0–10 wt.%. Transmission electron microscopy, inductively coupled plasma atomic emission spectrometry, X-ray photoelectron spectroscopy, Raman spectroscopy, and nitrogen physisorption measurements revealed that the Pt/C materials obtained by this method possess high surface areas (350–500 m2 g−1), narrow Pt nanoparticle size distributions (6 ± 3 nm) and nanocrystalline graphite –like carbon character. By immobilization of glucose oxidase on the surface of a 4 wt.% Pt/C electrocatalyst prepared by this route, a very sensitive amperometric glucose biosensor was obtained (response time <2 min, sensitivity 1.9 mA M−1; and a linear response with glucose concentration up to 10 mM). The simplicity and versatility of the described synthetic method suggests its application to the preparation of carbon supported noble metal catalysts including palladium/C and gold/C. (author)

  10. Synthesis of β-SiC nanowires by ball milled nanoparticles of silicon and carbon

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Pengchao, E-mail: kangpc@hit.edu.cn [Materials Science and Engineering School, Harbin Institute of Technology, P.O.B. 433, Harbin 150001 (China); Zhang, Bin; Wu, Gaohui; Gou, Huasong; Chen, Guoqin; Jiang, Longtao [Materials Science and Engineering School, Harbin Institute of Technology, P.O.B. 433, Harbin 150001 (China); Mula, Suhrit [Department of Metallurgical and Materials Engineering, Indian Institute of Technology Roorkee, Roorkee 247667 (India)

    2014-08-01

    Highlights: • The β-SiC nanowires were synthesized only use milled Si and C nanoparticles. • No catalyst was used in this process. • The grown mechanism of β-SiC nanowires is nanoparticles self-assembly and solid–solid reaction. • This notion, together with the nanowires synthesis are expected to apply opens up other semiconductor nanomaterials. - Abstract: In the present investigation, we report a simple and new technique to synthesize silicon carbide nanowires by high energy ball milling of silicon and carbon powders followed by annealing at elevated temperatures. The detailed structural analysis was carried out by X-ray diffraction, scanning and transmission electron microscopy, and FT-IR analysis. Nanocrystalline silicon particles were detected to be covered by amorphous carbon after milling. This typical structure was transformed to β-SiC nanowires during annealing by new growth mechanism. The β-SiC nanoparticles were found to be self-assembled one by one and formed a curly chain, and then rotated gradually in accordance to the same crystal orientation along the β-SiC [1 1 1] direction.

  11. Single-step synthesis of nanocomposite of copper and carbon nanoparticles using arc discharge in liquid nitrogen

    International Nuclear Information System (INIS)

    A new strategy for single-step synthesis of copper and carbon nanoparticle composite by arc discharge in liquid nitrogen was proposed. The synthesized products consist of carbon nanoparticles (CNPs) which include multi-walled carbon nanotubes (MWCNTs), single-walled carbon nanohorns (SWCNHs) and multi-shelled carbon nanocapsules (MSCNCs) containing Cu clusters inside. Evidence of transmission electron microscopic analyses reveal that under with arc current of 180 A arc discharge between copper and graphite electrodes in liquid nitrogen could provide MSCNCs with narrow size distribution in a range of 70-150 nm. Meanwhile, MWCNTs with diameter of 20-40 nm and length of 150-350 nm became selectively synthesized under the condition of discharge in liquid nitrogen with arc current of 100 A. Spectroscopic analyses confirm that copper nanoparticles are cuprite while BET analyses also reveal that the synthesized nanocomposite possess acceptably high specific surface area.

  12. Synthesis, Characterization, and Photocatalytic Properties of Sulfur- and Carbon-Codoped TiO2 Nanoparticles.

    Science.gov (United States)

    Ivanov, S; Barylyak, A; Besaha, K; Bund, A; Bobitski, Y; Wojnarowska-Nowak, R; Yaremchuk, I; Kus-Liśkiewicz, M

    2016-12-01

    One-step TiO2 nanoparticle synthesis based on the interaction between thiourea and metatitanic acid is applied for sulfur and carbon anatase codoping. The synthesis of the doped TiO2 has been monitored by means of differential thermal analysis and thermogravimetric analysis (DTA-TG), which allows determining the optimal thermal conditions for the process. Electron microscopy showed micrometer-sized (5-15 μm) randomly distributed crystal aggregates, consisting of many 15-40-nm TiO2 nanoparticles. The obtained phase composition and chemical states of the doping elements are analyzed by means of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared (IR) and Raman spectroscopies, and electron paramagnetic resonance (EPR). XRD displays in both samples (doped and pristine) the existence of only one crystalline phase-the tetragonal modification of TiO2-anatase. Further data assessment by means of Rietveld refinement allowed detection of a slight c lattice parameter and volume increase related to incorporation of the doping elements. XPS demonstrated the presence of carbon and sulfur as doping elements in the material. It was confirmed that carbon is in elemental form and also present in oxygen-containing compounds, which are adsorbed on the particle surface. The binding energy for sulfur electron core shell corresponds to the established data for sulfate compounds, where sulfur is in 6+ oxidation state. The synthesized S- and C-codoped TiO2 showed excellent photocatalytic performance during the degradation of organic dyes (rhodamine B, methylene blue), gas-phase oxidation of ethanol under visible light, and photocatalytic hydrogen generation from ethanol under ultraviolet light. PMID:26969593

  13. Synthesis, Characterization, and Photocatalytic Properties of Sulfur- and Carbon-Codoped TiO2 Nanoparticles

    Science.gov (United States)

    Ivanov, S.; Barylyak, A.; Besaha, K.; Bund, A.; Bobitski, Y.; Wojnarowska-Nowak, R.; Yaremchuk, I.; Kus-Liśkiewicz, M.

    2016-03-01

    One-step TiO2 nanoparticle synthesis based on the interaction between thiourea and metatitanic acid is applied for sulfur and carbon anatase codoping. The synthesis of the doped TiO2 has been monitored by means of differential thermal analysis and thermogravimetric analysis (DTA-TG), which allows determining the optimal thermal conditions for the process. Electron microscopy showed micrometer-sized (5-15 μm) randomly distributed crystal aggregates, consisting of many 15-40-nm TiO2 nanoparticles. The obtained phase composition and chemical states of the doping elements are analyzed by means of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared (IR) and Raman spectroscopies, and electron paramagnetic resonance (EPR). XRD displays in both samples (doped and pristine) the existence of only one crystalline phase—the tetragonal modification of TiO2—anatase. Further data assessment by means of Rietveld refinement allowed detection of a slight c lattice parameter and volume increase related to incorporation of the doping elements. XPS demonstrated the presence of carbon and sulfur as doping elements in the material. It was confirmed that carbon is in elemental form and also present in oxygen-containing compounds, which are adsorbed on the particle surface. The binding energy for sulfur electron core shell corresponds to the established data for sulfate compounds, where sulfur is in 6+ oxidation state. The synthesized S- and C-codoped TiO2 showed excellent photocatalytic performance during the degradation of organic dyes (rhodamine B, methylene blue), gas-phase oxidation of ethanol under visible light, and photocatalytic hydrogen generation from ethanol under ultraviolet light.

  14. Synthesis and characterization of Ag nanoparticles decorated mesoporous sintered activated carbon with antibacterial and adsorptive properties

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wenxia; Xiao, Kaijun, E-mail: fekjxiao@scut.edu.cn; He, Tinglin; Zhu, Liang, E-mail: zhuliang@scut.edu.cn

    2015-10-25

    In this study, the sliver nanoparticles (AgNPs) immobilized on the sintered activated carbon (Ag/SAC) were synthesized by the ultrasonic-assisted impregnation method and were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD) and nitrogen adsorption. SEM showed that the AgNPs were well embedded in the SAC and immersion time had an important influence on final morphologies of AgNPs. Longer immersing duration caused significant aggregation of the AgNPs. The XRD data revealed that the successful synthesis of AgNPs on the SAC and immobilizing AgNPs on sintered active carbon did not change the crystalline degree of SAC. Texture characteristics were determined by analysis of the N{sub 2}/77 K isotherms. The minimum inhibitory concentration (MIC) of Ag/SAC against Escherichia coli (DH5α) and Staphyloccocus aureus (ATCC 29213) was evaluated by a broth dilution method. MICs such as 5 mg/L (against E. coli) and 10 mg/L (against S. aureus) suggest that Ag/SAC have predominant antibacterial activity compared to active carbon. - Highlights: • Sintered active carbon (SAC) was coated with Ag via a facile approach. • The Ag/SAC exhibit good adsorption properties and excellent antibacterial effects. • The Ag/SAC was durable and stable in the application of water purification.

  15. 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.

  16. Trends in the Microwave-Assisted Synthesis of Metal Oxide Nanoparticles Supported on Carbon Nano tubes and Their Applications

    International Nuclear Information System (INIS)

    The study of coating carbon nano tubes with metal/oxides nanoparticles is now becoming a promising and challenging area of research. To optimize the use of carbon nano tubes in various applications, it is necessary to attach functional groups or other nano structures to their surface. The combination of the distinctive properties of carbon nano tubes and metal/oxides is expected to be applied in field emission displays, nano electronic 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-nano tube-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.

  17. Synthesis of carbon encapsulated SiO2 nanoparticles from rice husk and its application in solar to steam conversion

    Science.gov (United States)

    Mufti, Nandang; Lestari, Nurhayati A.; Suciani, Erlin; Fuad, Abdulloh; Diantoro, Markus

    2016-03-01

    Steam is important in many technological applications including sterilization of medical devices, cleaning, and power generating. In general, steam can be produced by boiling water at high temperature. In new technology, solar can convert water directly into steam even at low temperature by using nanoparticles. In this research we study solar to steam conversion of carbon encapsulated SiO2 nanoparticles (SiO2@C) synthesized from rice husk. SiO2 nanoparticles were synthesized using alkali extraction and sol-gel methods. While synthesis of carbon encapsulated SiO2 nanoparticles was done by sonochemical method with glucose as source of carbon. The samples have been characterized by XRF, SEM-EDX, and XRD. The effectivity of solar steam conversion performed by measuring time dependent of temperature and pressure. XRF and XRD results shown that SiO2 nanoparticles have purity of 97.2% inn amorphous phase. Carbon encapsulated SiO2 nanoparticles (SiO2@C) have successfully synthesized indicating by NaOH base test. The morphology of SiO2@C is agglomerated with average particle size around 20 nm. The measurement of solar to steam conversion showed that increasing carbon concentration of SiO2@C rises steam production with indicated by increasing temperature and pressure of steam.

  18. One-step facile synthesis of carbon-supported PdAu nanoparticles and their electrochemical property and stability

    International Nuclear Information System (INIS)

    Graphical abstract: Well-crystallized PdAu alloy nanoparticles with the average size of 2–5 nm supported on Ketjen Black (KB) were successfully fabricated from the metal wire electrodes via a one-step solution plasma process in water at atmospheric pressure. Multi-scan cyclic voltammetry showed they have better electrochemical stability in alkaline than in acidic solution. - Highlights: • Carbon-supported PdAu nanoparticles were fabricated by a solution plasma technique. • As-obtained PdAu nanoparticles were confirmed to be alloy. • PdAu nanoparticles have good electrochemical activities and stabilities. • PdAu nanoparticles in alkaline have better stability than that in acidic solution. - Abstract: Well-crystallized PdAu nanoparticles supported on Ketjen Black (KB) were successfully fabricated when both Pd and Au wires were served as the electrode pair by a solution plasma technique at atmospheric pressure. The synthesis of PdAu nanoparticles was almost simultaneous with their dispersion on KB. As-obtained PdAu nanoparticles were confirmed to be alloy by ultraviolet–visible spectrophotometer, transmission electron microscopy (TEM) and energy dispersive X-ray analysis (EDX) of each particle. PdAu nanoparticles with the average diameter of 2–5 nm were equably distributed on KB. PdAu nanoparticles showed good electrocatalytic activity both in acidic and alkaline solution corresponding to their obvious oxidation and reduction features. PdAu nanoparticles have improved electrochemical stability compared with the electrochemical properties of Pd and Au nanoparticles mixture after long time multi-scan cyclic voltammetry. Multi-scan cyclic voltammetry also presented the PdAu nanoparticles in alkaline solution have better stability than that in acidic solution. Thus as-obtained PdAu alloy nanoparticles would become a promising electrocatalysts for fuel cells or Li-air batteries. This novel process showed its potential applications in designing optimization of

  19. One-step facile synthesis of carbon-supported PdAu nanoparticles and their electrochemical property and stability

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Xiulan, E-mail: whoxiulan@163.com [College of Materials Science and Engineering, Nanjing Tech University (China); Shi, Junjun; Zhang, Jianbo [College of Materials Science and Engineering, Nanjing Tech University (China); Tang, Weiping [Shanghai Institute of Space Power Sources, Shanghai (China); Zhu, Haikui; Shen, Xiaodong [College of Materials Science and Engineering, Nanjing Tech University (China); Saito, Nagahiro [Department of Materials, Physics and Energy Engineering, Graduate School of Engineering, Nagoya University (Japan)

    2015-01-15

    Graphical abstract: Well-crystallized PdAu alloy nanoparticles with the average size of 2–5 nm supported on Ketjen Black (KB) were successfully fabricated from the metal wire electrodes via a one-step solution plasma process in water at atmospheric pressure. Multi-scan cyclic voltammetry showed they have better electrochemical stability in alkaline than in acidic solution. - Highlights: • Carbon-supported PdAu nanoparticles were fabricated by a solution plasma technique. • As-obtained PdAu nanoparticles were confirmed to be alloy. • PdAu nanoparticles have good electrochemical activities and stabilities. • PdAu nanoparticles in alkaline have better stability than that in acidic solution. - Abstract: Well-crystallized PdAu nanoparticles supported on Ketjen Black (KB) were successfully fabricated when both Pd and Au wires were served as the electrode pair by a solution plasma technique at atmospheric pressure. The synthesis of PdAu nanoparticles was almost simultaneous with their dispersion on KB. As-obtained PdAu nanoparticles were confirmed to be alloy by ultraviolet–visible spectrophotometer, transmission electron microscopy (TEM) and energy dispersive X-ray analysis (EDX) of each particle. PdAu nanoparticles with the average diameter of 2–5 nm were equably distributed on KB. PdAu nanoparticles showed good electrocatalytic activity both in acidic and alkaline solution corresponding to their obvious oxidation and reduction features. PdAu nanoparticles have improved electrochemical stability compared with the electrochemical properties of Pd and Au nanoparticles mixture after long time multi-scan cyclic voltammetry. Multi-scan cyclic voltammetry also presented the PdAu nanoparticles in alkaline solution have better stability than that in acidic solution. Thus as-obtained PdAu alloy nanoparticles would become a promising electrocatalysts for fuel cells or Li-air batteries. This novel process showed its potential applications in designing optimization of

  20. Pulsed Plasma Synthesis of Iron and Nickel Nanoparticles Coated by Carbon for Medical Applications

    Science.gov (United States)

    Abdullaeva, Zhypargul; Omurzak, Emil; Iwamoto, Chihiro; Ihara, Hirotaka; Subban Ganapathy, Hullathy; Sulaimankulova, Saadat; Koinuma, Michio; Mashimo, Tsutomu

    2013-01-01

    Fe and Ni magnetic nanoparticles coated by carbon were synthesized between the Fe-Fe and Ni-Ni metal electrodes, submerged in ethanol using pulsed plasma in a liquid method. Iron coated carbon (Fe@C) nanoparticles have an average size of 32 nm, and Ni@C nanoparticles are 40 nm. Obtained samples exhibit a well-defined crystalline structure of the inner Fe and Ni cores, encapsulated in the graphitic carbon coatings. Cytotoxicity studies performed on the MCF-7 (breast cancer) cell line showed small toxicity about 88-74% at 50 µg/mL of Fe@C and Ni@C nanoparticles, which can be significant criteria for use them in medical cancer treatment. In addition, appropriate sizes, good magnetic properties and well-organized graphitic carbon coatings are highlight merits of Fe@C and Ni@C nanoparticles synthesized by pulsed plasma.

  1. Synthesis of functional diamond-like carbon nanocomposite films containing titanium dioxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Kuo-Cheng [Department of Chemical Engineering, National Cheng Kung University, 1 University Road, Tainan 701, Taiwan (China); Hong, Franklin Chau-Nan, E-mail: hong@mail.ncku.edu.t [Department of Chemical Engineering, National Cheng Kung University, 1 University Road, Tainan 701, Taiwan (China); Center for Micro/Nano Science and Technology, National Cheng Kung University, Taiwan (China); Advanced Optoelectronic Technology Center, National Cheng Kung University, Taiwan (China)

    2010-10-01

    Synthesis of diamond-like carbon (DLC) films with UV-induced-hydrophilicity function was studied by inductively-coupled plasma (ICP) chemical vapor deposition. Titanium tetraisopropoxide (TTIP) and oxygen gases were employed as the precursors to deposit diamond-like nanocomposite films containing titanium dioxide (TiO{sub 2}) nanoparticles. X-ray diffraction and high-resolution transmission electron microscopy revealed that TiO{sub 2} nanocrystallites were formed in the DLC films when oxygen concentration was higher than TTIP concentration during deposition. The DLC nanocomposite film was hydrophobic without ultraviolet (UV) irradiation, and became highly hydrophilic under UV irradiation, exhibiting the self-cleaning effect. A very broad peak centered at 1580 cm{sup -1} was observed in the Raman spectra confirming the formation of DLC films. The hardness of the film was about 8 GPa with a stress of 3 GPa. ICP was essential in forming the photocatalytic TiO{sub 2} nanoparticles in the DLC matrix.

  2. Ferric oxide nanoparticles decorated carbon nanotubes and carbon nanofibers: From synthesis to enhanced removal of phenol

    Directory of Open Access Journals (Sweden)

    Hamza A. Asmaly

    2015-09-01

    Full Text Available In this work, ferric oxide nanoparticle decorated carbon fibers and carbon nanotubes (CNF/Fe2O3 and CNT/Fe2O3 were synthesized and characterized by scanning electron microscopy (SEM, thermogravimetric analysis (TGA, energy dispersive X-ray spectroscopy (EDS, transmission electron microscopy (TEM, X-ray diffraction (XRD, zeta potential and BET surface area analyzer. The prepared nanocomposites were evaluated or the removal of phenol ions from aqueous solution. The effects of experimental parameters, such as shaking speed, pH, contact time, adsorbent dosage and initial concentration, were evaluated for the phenol removal efficiency. The adsorption experimental data were represented by both the Langmuir and Freundlich isotherm models. The Langmuir isotherm model best fitted the data on the adsorption of phenol, with a high correlation coefficient. The adsorption capacities, as determined by the Langmuir isotherm model were 0.842, 1.098, 1.684 and 2.778 mg/g for raw CNFs, raw CNTs, CNF–Fe2O3 and CNT–Fe2O3, respectively.

  3. Catalytic pyrogenation synthesis of C/Ni composite nanoparticles: controllable carbon structures and high permittivities

    Energy Technology Data Exchange (ETDEWEB)

    Lu, B; Huang, H; Dong, X L; Lei, J P, E-mail: dongxl@dlut.edu.c [School of Materials Science and Engineering, Dalian University of Technology, Dalian, Liaoning 116024 (China)

    2010-03-17

    Catalytic pyrogenation of methane gas in the presence of Ni nanoparticles was employed to synthesize C/Ni composite nanoparticles at various reaction temperatures. The Ni nanoparticles prepared by the arc-discharge method served as a catalyst to decompose the hydrocarbon molecules and also provided isolated templates for the formation of carbon nanocapsules at 400 and 500 {sup 0}C or multi-walled carbon nanotubes at 600 and 650 {sup 0}C. The generation and growth mechanism of the carbon shells are discussed on the basis of structure evolution. By dispersing the nanoparticles homogeneously into a paraffin matrix, the electromagnetic parameters of the nanoparticles have been investigated in the frequency range 2-18 GHz. The samples exhibit high permittivities varying with the microstructures of the nanoparticles. The relationship between the dielectric properties and diverse carbon structures is indicated. The high permittivities of the nanoparticles are attributed to the better conductivity of the carbon shells and the charge polarizations at the defects or interfaces between metal cores and carbon shells.

  4. White carbon: Fluorescent carbon nanoparticles with tunable quantum yield in a reproducible green synthesis

    Science.gov (United States)

    Meiling, Till T.; Cywiński, Piotr J.; Bald, Ilko

    2016-01-01

    In this study, a new reliable, economic, and environmentally-friendly one-step synthesis is established to obtain carbon nanodots (CNDs) with well-defined and reproducible photoluminescence (PL) properties via the microwave-assisted hydrothermal treatment of starch and Tris-acetate-EDTA (TAE) buffer as carbon sources. Three kinds of CNDs are prepared using different sets of above mentioned starting materials. The as-synthesized CNDs: C-CND (starch only), N-CND 1 (starch in TAE) and N-CND 2 (TAE only) exhibit highly homogenous PL and are ready to use without need for further purification. The CNDs are stable over a long period of time (>1 year) either in solution or as freeze-dried powder. Depending on starting material, CNDs with PL quantum yield (PLQY) ranging from less than 1% up to 28% are obtained. The influence of the precursor concentration, reaction time and type of additives on the optical properties (UV-Vis absorption, PL emission spectrum and PLQY) is carefully investigated, providing insight into the chemical processes that occur during CND formation. Remarkably, upon freeze-drying the initially brown CND-solution turns into a non-fluorescent white/slightly brown powder which recovers PL in aqueous solution and can potentially be applied as fluorescent marker in bio-imaging, as a reduction agent or as a photocatalyst. PMID:27334409

  5. White carbon: Fluorescent carbon nanoparticles with tunable quantum yield in a reproducible green synthesis

    Science.gov (United States)

    Meiling, Till T.; Cywiński, Piotr J.; Bald, Ilko

    2016-06-01

    In this study, a new reliable, economic, and environmentally-friendly one-step synthesis is established to obtain carbon nanodots (CNDs) with well-defined and reproducible photoluminescence (PL) properties via the microwave-assisted hydrothermal treatment of starch and Tris-acetate-EDTA (TAE) buffer as carbon sources. Three kinds of CNDs are prepared using different sets of above mentioned starting materials. The as-synthesized CNDs: C-CND (starch only), N-CND 1 (starch in TAE) and N-CND 2 (TAE only) exhibit highly homogenous PL and are ready to use without need for further purification. The CNDs are stable over a long period of time (>1 year) either in solution or as freeze-dried powder. Depending on starting material, CNDs with PL quantum yield (PLQY) ranging from less than 1% up to 28% are obtained. The influence of the precursor concentration, reaction time and type of additives on the optical properties (UV-Vis absorption, PL emission spectrum and PLQY) is carefully investigated, providing insight into the chemical processes that occur during CND formation. Remarkably, upon freeze-drying the initially brown CND-solution turns into a non-fluorescent white/slightly brown powder which recovers PL in aqueous solution and can potentially be applied as fluorescent marker in bio-imaging, as a reduction agent or as a photocatalyst.

  6. Short time synthesis of high quality carbon nanotubes with high rates by CVD of methane on continuously emerged iron nanoparticles

    International Nuclear Information System (INIS)

    We report the variation of yield and quality of carbon nanotubes (CNTs) grown by chemical vapor deposition (CVD) of methane on iron oxide-MgO at 900-1000 deg. C for 1-60 min. The catalyst was prepared by impregnation of MgO powder with iron nitrate, dried, and calcined at 300 deg. C. As calcined and unreduced catalyst in quartz reactor was brought to the synthesis temperature in helium flow in a few minutes, and then the flow was switched to methane. The iron oxide was reduced to iron nanoparticles in methane, while the CNTs were growing. TEM micrographs, in accordance with Raman RBM peaks, indicate the formation of mostly single wall carbon nanotubes of about 1.0 nm size. High quality CNTs with IG/ID Raman peak ratio of 14.5 are formed in the first minute of CNTs synthesis with the highest rate. Both the rate and quality of CNTs degrades with increasing CNTs synthesis time. Also CNTs quality sharply declines with temperature in the range of 900-1000 deg. C, while the CNTs yield passes through a maximum at 950 deg. C. About the same CNTs lengths are formed for the whole range of the synthesis times. A model of continuous emergence of iron nanoparticle seeds for CNTs synthesis may explain the data. The data can also provide information for continuous production of CNTs in a fluidized bed reactor.

  7. Hydrothermal carbon spheres containing silicon nanoparticles: synthesis and lithium storage performance.

    Science.gov (United States)

    Demir Cakan, Rezan; Titirici, Maria-Magdalena; Antonietti, Markus; Cui, Guanglei; Maier, Joachim; Hu, Yong-Sheng

    2008-08-28

    Spherically shaped carbon/silicon nanocomposites have been obtained in a one-step procedure using hydrothermal carbonization of glucose in the presence of commercially available silicon nanoparticles and have been tested electrochemically as an anode material for lithium-ion batteries. PMID:18685768

  8. Synthesis of zinc oxide nanoparticles on graphene-carbon nanotube hybrid for glucose biosensor applications.

    Science.gov (United States)

    Hwa, Kuo-Yuan; Subramani, Boopathi

    2014-12-15

    Synthesis of zinc oxide nanoparticles incorporated graphene-carbon nanotubes hybrid (GR-CNT-ZnO) through a simple, one-pot method is demonstrated. The as-synthesized GR-CNT-ZnO composite is applied to fabricate an enzyme based glucose biosensor. The GOx immobilized on GR-CNT-ZnO composite exhibits well-defined redox peaks with a peak potential separation (ΔEp) of about 26 mV with enhanced peak currents, indicating a fast electron transfer at the modified electrode surface. The cyclic voltammetry measurements revealed that the modified film has high electrocatalytic ability towards glucose detection in the presence of oxygen. The proposed sensor has a wide linear detection range from 10 μM to 6.5 mM of glucose with a limit of detection (LOD) of 4.5 (±0.08) μM. In addition, the sensor possessed appreciable repeatability, reproducibility and remarkable stability for the sensitive determination of glucose. The practicality of this sensor has been demonstrated in human serum samples, with results being in good agreement with those determined using a standard photometric method. PMID:24997365

  9. Synthesis of Metal Nanoparticle-decorated Carbon Nanotubes under Ambient Conditions

    Science.gov (United States)

    Lin, Yi; Watson, Kent A.; Ghose, Sayata; Smith, Joseph G.; Connell, John W.

    2008-01-01

    This viewgraph presentation reviews the production of Metal Nanoparticle-decorated carbon Nanotubes. Multi-walled carbon nanotubes (MWCNTs) were efficiently decorated with metal nanoparticles (e.g. Ag, Pt, etc.) using the corresponding metal acetate in a simple mixing process without the need of chemical reagents or further processing. The conversion of acetate compounds to the corresponding metal reached over 90%, forming nanoparticles with average diameters less than 10 nm under certain conditions. The process was readily scalable allowing for the convenient preparation of multi-gram quantities of metal nanoparticle-decorated MWCNTs in a matter of a few minutes. These materials are under evaluation for a variety of electrical and catalytic applications. The preparation and characterization of these materials will be presented. The microscopic views of the processed MWCNTs are shown

  10. Synthesis of Cu, Zn and Cu/Zn brass alloy nanoparticles from metal amidinate precursors in ionic liquids or propylene carbonate with relevance to methanol synthesis

    Science.gov (United States)

    Schütte, Kai; Meyer, Hajo; Gemel, Christian; Barthel, Juri; Fischer, Roland A.; Janiak, Christoph

    2014-02-01

    Microwave-induced decomposition of the transition metal amidinates {[Me(C(NiPr)2)]Cu}2 (1) and [Me(C(NiPr)2)]2Zn (2) in the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm][BF4]) or in propylene carbonate (PC) gives copper and zinc nanoparticles which are stable in the absence of capping ligands (surfactants) for more than six weeks. Co-decomposition of 1 and 2 yields the intermetallic nano-brass phases β-CuZn and γ-Cu3Zn depending on the chosen molar ratios of the precursors. Nanoparticles were characterized by high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM), dynamic light scattering and powder X-ray diffractometry. Microstructure characterizations were complemented by STEM with spatially resolved energy-dispersive X-ray spectrometry and X-ray photoelectron spectroscopy. Synthesis in ILs yields significantly smaller nanoparticles than in PC. β-CuZn alloy nanoparticles are precursors to catalysts for methanol synthesis from the synthesis gas H2/CO/CO2 with a productivity of 10.7 mol(MeOH) (kg(Cu) h)-1.Microwave-induced decomposition of the transition metal amidinates {[Me(C(NiPr)2)]Cu}2 (1) and [Me(C(NiPr)2)]2Zn (2) in the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm][BF4]) or in propylene carbonate (PC) gives copper and zinc nanoparticles which are stable in the absence of capping ligands (surfactants) for more than six weeks. Co-decomposition of 1 and 2 yields the intermetallic nano-brass phases β-CuZn and γ-Cu3Zn depending on the chosen molar ratios of the precursors. Nanoparticles were characterized by high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM), dynamic light scattering and powder X-ray diffractometry. Microstructure characterizations were complemented by STEM with spatially resolved energy-dispersive X-ray spectrometry and X-ray photoelectron spectroscopy. Synthesis in ILs yields significantly smaller nanoparticles than in PC.

  11. 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.

  12. Synthesis of CaCO3 nanoparticles by carbonation of lime solutions in reverse micellar systems

    NARCIS (Netherlands)

    Heeres, H.J.; Jain, R.; Mehra, A.; Dagaonkar, M.V.

    2004-01-01

    Application of reverse micelles for the synthesis of nano-sized calcium carbonate particles in different solvents (cyclohexane, decane and heptane) has been investigated. The effect of the mole ratio of water-to-surfactant (R) and type of solvent has been studied on the size and nature of the carbon

  13. Arc-Discharge Synthesis of Iron Encapsulated in Carbon Nanoparticles for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    S. Chaitoglou

    2014-01-01

    Full Text Available The objective of the present work is to improve the protection against the oxidation that usually appears in core@shell nanoparticles. Spherical iron nanoparticles coated with a carbon shell were obtained by a modified arc-discharge reactor, which permits controlling the diameter of the iron core and the carbon shell of the particles. Oxidized iron nanoparticles involve a loss of the magnetic characteristics and also changes in the chemical properties. Our nanoparticles show superparamagnetic behavior and high magnetic saturation owing to the high purity α-Fe of core and to the high core sealing, provided by the carbon shell. A liquid iron precursor was injected in the plasma spot dragged by an inert gas flow. A fixed arc-discharge current of 40 A was used to secure a stable discharge, and several samples were produced at different conditions. Transmission electron microscopy indicated an iron core diameter between 5 and 9 nm. Selected area electron diffraction provided evidences of a highly crystalline and dense iron core. The magnetic properties were studied up to 5 K temperature using a superconducting quantum interference device. The results reveal a superparamagnetic behaviour, a narrow size distribution (σg=1.22, and an average diameter of 6 nm for nanoparticles having a blocking temperature near 40 K.

  14. Synthesis and characterization of platinum nanoparticles on single-walled Carbon nanotube 'nanopaper' support

    International Nuclear Information System (INIS)

    We prepared several samples of carbon-nanotube-supported Pt nanoparticles that are potentially promising electrocatalysts for hydrogen fuel cells. Commercially obtained single-walled carbon nanotubes (SWNTs) were characterized by Raman Spectroscopy, SEM, TEM, EDS, and XANES. This multi-technique characterization allowed us to quantify the size and composition of metal impurities (Mo, Co) in SWNTs, to choose the best method to remove them, and characterize the effectiveness of their removal. After synthesizing a 'nanopaper' (10-20 micrometer thick, free standing sheets of self-assembled SWNTs) we decorated it with Pt nanoparticles by electroless deposition. Formation of Pt nanoparticles was verified by EXAFS, and quantitative information about their size and structure was obtained.

  15. Green synthesis of carbon-supported nanoparticle catalysts by physical vapor deposition on soluble powder substrates

    OpenAIRE

    Hee-Young Park; Injoon Jang; Namgee Jung; Young-Hoon Chung; Jae Yoon Ryu; In Young Cha; Hyung Juhn Kim; Jong Hyung Jang; Sung Jong Yoo

    2015-01-01

    Metal and metal oxide nanoparticles (NPs) supported on high surface area carbon (NP/Cs) were prepared by the physical vapor deposition of bulk materials on an α-D-glucose (Glu) substrate, followed by the deposition of the NPs on carbon supports. Using Glu as a carrier for the transport of NPs from the bulk materials to the carbon support surfaces, ultrafine NPs were obtained, exhibiting a stabilizing effect through OH moieties on the Glu surfaces. This stabilizing effect was strong enough to ...

  16. Solvothermal synthesis of green-fluorescent carbon nanoparticles and their application

    International Nuclear Information System (INIS)

    A novel solvothermal approach to synthesize green-fluorescent carbon nanoparticles (CNPs) was developed using L-ascorbic acid as the carbon source, glycol and triple distilled water as the solvent. The CNPs emit strong green fluorescence under UV irradiation, and the fluorescence intensity showed a good linear relationship with pH value within a certain range. Direct yeast cell labeling was achieved through cell endocytosis of these CNPs. - Highlights: ► A one-step approach to synthesize fluorescent carbon nanoparticles was developed. ► A linear relationship between fluorescence intensity and pH value was observed. ► Direct labeling of yeast cells was realized successfully with the CNPs.

  17. CO2 assisted synthesis of highly dispersed Co3O4 nanoparticles on mesoporous carbon for lithium ion battery

    International Nuclear Information System (INIS)

    Graphical abstract: Co3O4 nanoparticles were uniformly dispersed onto the mesoporous carbon support (Co3O4/mC) using a facile process in CO2–expanded ethanol (CE) solution. Compared with Co3O4/mC-E synthesized in pure ethanol, the Co3O4/mC-CE exhibited better cycle performance which could be attributed to the synergistic effects between the superior structures of mesoporous C support and the highly dispersed Co3O4 nanoparticles. - Highlights: • Co3O4 nanoparticles were highly dispersed on mesoporous C in CE system. • The synthesis avoided the use of precipitants and aggregation of Co3O4 particles. • Co3O4/mC exhibited better cycle performance than the reference sample. • The synergistic effects of the mC and Co3O4 resulted in the improved performance. - Abstract: Co3O4 nanoparticles were uniformly dispersed onto the mesoporous carbon support (Co3O4/mC) using a facile process in CO2–expanded ethanol (CE) solution. During the synthesis, CO2 played the dual roles, one is to provide a simple physical expansion to evenly disperse the precursors onto the mesoporous carbon support, and the other is to offer some chemical groups such as CO32− to facilitate the complete and uniform deposition through the coordination to the metallic cations with these anions. When used as anode material for lithium ion batteries (LIBs), the Co3O4/mC synthesized in CO2-expanded ethanol solution exhibited larger surface area and better cycle performance compared with the reference sample synthesized in pure ethanol. The enhanced cycle performance could be attributed to the synergistic effects between the superior structures of mesoporous C support and the highly dispersed Co3O4 nanoparticles. More importantly, the synthesis of Co3O4/mC composite in CE solution was green and highly efficient, avoiding the use of precipitant and the aggregation of Co3O4, which would definitely enrich the strategies for the fabrication of carbon-based transition-metal oxide composites with great

  18. Laser assisted synthesis of carbon nanoparticles with controlled viscosities for printing applications.

    Science.gov (United States)

    Bagga, K; McCann, R; Wang, M; Stalcup, A; Vázquez, M; Brabazon, D

    2015-06-01

    High-quality carbon nanoparticles with controlled viscosity and high aqueous stability were prepared by liquid-phase laser ablation of a graphite target in deionized water. The size distribution was found to vary from 5nm to 50nm with mean size of 18nm, in the absence of any reducing chemical reagents. Efficient generation of short chain polyynes was recorded for high laser repetition rates. Homogeneous and stable nanoparticle suspensions with viscosities ranging from 0.89 to 12mPa.s were obtained by suspending the nanoparticles in different solvent mixtures such as glycerol-water and isopropanol-water. Optical properties were investigated by absorption and photoluminescence spectroscopy. Raman spectroscopy confirmed graphitic-like structure of nanoparticles and the surface chemistry was revealed by Fourier-transform infrared spectroscopy demonstrating sufficient electrostatic stabilization to avoid particle coagulation or flocculation. This paper present an exciting alternative method to engineer carbon nanoparticles and their potential use as a ligand-free nano-ink for ink jet printing (jetting) applications. PMID:25465202

  19. Synthesis and characterization of silver-carbon nanoparticles produced by high-current pulsed arc

    Energy Technology Data Exchange (ETDEWEB)

    Maya, F., E-mail: fermr@correo.unam.m [Departamento de Microscopia Electronica, Centro de Investigacion en Materiales Avanzados, Miguel de Cervantes 120, Chihuahua, Chih., CP 3110 (Mexico); Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, 04510 (Mexico); Muhl, S.; Pena, O. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, 04510 (Mexico); Miki-Yoshida, M. [Departamento de Microscopia Electronica, Centro de Investigacion en Materiales Avanzados, Miguel de Cervantes 120, Chihuahua, Chih., CP 3110 (Mexico)

    2009-12-31

    In this paper, we report the formation of silver-carbon encapsulated metal nanoparticles (EMN's) using a high-current pulsed arc system in an argon atmosphere. The deposits were studied by Optical Extinction Spectroscopy (OES), X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM); the chemical analysis of the deposits was performed using Energy Dispersion X-ray spectroscopy (EDX). Using the total nanoparticle diameter, the bulk crystalline density of silver and an estimate amorphous carbon (a-C) density we have calculated the size of the silver nucleus and the thickness of the a-C coating as a function of the argon gas pressure. The OES spectra of the EMN's exhibited two peaks characteristic of the Surface Plasmon Resonance (SPR) of elongated/very close silver nanoparticles; a subsequent thermal annealing strongly increased the SPR peaks. The double peak SPR spectra were modeled using calculations based on the existence of silver nanoparticles in the form of prolate spheroids. The main advantage of our preparation method is that the metal nanoparticles are encapsulated in a-C from the beginning and this layer acts as an efficient chemical barrier.

  20. Synthesis and characterization of silver-carbon nanoparticles produced by high-current pulsed arc

    International Nuclear Information System (INIS)

    In this paper, we report the formation of silver-carbon encapsulated metal nanoparticles (EMN's) using a high-current pulsed arc system in an argon atmosphere. The deposits were studied by Optical Extinction Spectroscopy (OES), X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM); the chemical analysis of the deposits was performed using Energy Dispersion X-ray spectroscopy (EDX). Using the total nanoparticle diameter, the bulk crystalline density of silver and an estimate amorphous carbon (a-C) density we have calculated the size of the silver nucleus and the thickness of the a-C coating as a function of the argon gas pressure. The OES spectra of the EMN's exhibited two peaks characteristic of the Surface Plasmon Resonance (SPR) of elongated/very close silver nanoparticles; a subsequent thermal annealing strongly increased the SPR peaks. The double peak SPR spectra were modeled using calculations based on the existence of silver nanoparticles in the form of prolate spheroids. The main advantage of our preparation method is that the metal nanoparticles are encapsulated in a-C from the beginning and this layer acts as an efficient chemical barrier.

  1. Carbon nanotubes-supported palladium nanoparticles for the Suzuki reaction in supercritical carbon dioxide: A facile method for the synthesis of tetrasubstituted olefins

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A facile and efficient method for the synthesis of tetrasubstituted olefins in supercritical carbon dioxide was developed by using carbon nanotubes-supported palladium nanoparticles (Pd/CNTs) as the catalyst. Compared with common Pd/C, Pd/CNTs could more effectively catalyze the reaction of dibromo-substituted olefins with boronic acids, affording the corresponding tetrasubstituted olefins with moderate to good yields. This environmentally benign route with an easy-to-handle catalyst provides an appealing alternative to the currently available methods.

  2. Laser assisted synthesis of carbon nanoparticles with controlled viscosities for printing applications

    OpenAIRE

    Bagga, Komal; McCann, R.; Wang, M.; Stalcup, Apryll; Vazquez, Mercedes; Brabazon, Dermot

    2015-01-01

    High-quality carbon nanoparticles with controlled viscosity and high aqueous stability were prepared by liquid-phase laser ablation of a graphite target in deionized water. The size distribution was found to vary from 5 nm to 50 nm with mean size of 18 nm, in the absence of any reducing chemical reagents. Efficient generation of short chain polyynes was recorded for high laser repetition rates. Homogeneous and stable nanoparticle suspensions with viscosities ranging from 0.89 to 12 mPa.s were...

  3. Synthesis of honeycomb MnO2 nanospheres/carbon nanoparticles/graphene composites as electrode materials for supercapacitors

    Science.gov (United States)

    Xiong, Yachao; Zhou, Min; Chen, Hao; Feng, Lei; Wang, Zhao; Yan, Xinzhu; Guan, Shiyou

    2015-12-01

    Improving the electrochemical performance of manganese dioxide (MnO2) electrodes is of great significance for supercapacitors. In this study, a novel honeycomb MnO2 nanospheres/carbon nanoparticles/graphene composites has been fabricated through freeze-drying method. The honeycomb MnO2 nanospheres are well inserted and dispersed on the graphene. Carbon nanoparticles in the composites act as spacers to effectively prevent graphene from restacking and agglomeration, construct efficient 3D conducting architecture with graphene for honeycomb MnO2 nanospheres, and alleviate the aggregation of honeycomb MnO2 nanospheres by separating them from each other. As a result, such honeycomb MnO2 nanospheres/carbon nanoparticles/graphene composites display much improved electrochemical capacitive performance of 255 F g-1 at a current density of 0.5 A g-1, outstanding rate capability (150 F g-1 remained at a current density of 20 A g-1) and good cycling stability (83% of the initial capacitance retained after 1000 charge/discharge cycles). The strategy for the synthesis of these composites is very effective.

  4. Room-temperature synthesis and electrocatalysis of carbon nanotubes supported palladium–iron alloy nanoparticles

    International Nuclear Information System (INIS)

    Carbon nanotubes (CNTs) supported palladium–iron bimetallic nanoparticles (Pd–Fe/CNTs) catalyst is synthesized using palladium hexacyanoferrate (PdHCF) as reaction precursor. In this method, the negatively charged PdHCF nanoparticles self-assemble on the positively charged polydiallyldimethylammonium chloride (PDDA) functionalized CNTs through electrostatic interaction, and then are reduced to Pd–Fe alloy nanoparticles by sodium borohydride. The physicochemical properties of Pd–Fe/CNTs are investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). These structural analyses reveal that the Pd–Fe/CNTs catalyst possesses the high alloying degree and the small particle size. Electrochemical measurements show that the eletrocatalytic activity of the Pd–Fe/MWCNTs catalyst for the methanol oxidation is better than that of the Pd/CNTs catalyst, which originates from the synergistic effect between Pd atom and Fe atom

  5. Easy synthesis and imaging applications of cross-linked green fluorescent hollow carbon nanoparticles.

    Science.gov (United States)

    Fang, Youxing; Guo, Shaojun; Li, Dan; Zhu, Chengzhou; Ren, Wen; Dong, Shaojun; Wang, Erkang

    2012-01-24

    We propose an ingenious method for synthesizing cross-linked hollow fluorescent carbon nanoparticles (HFCNs) with green emission by simply mixing acetic acid, water, and diphosphorus pentoxide. This is an automatic method without external heat treatment to rapidly produce large quantities of HFCNs, in contrast to other syntheses of fluorescent carbon nanoparticles that required high temperature, complicated operations, or long reaction times. Characterizations of HFCNs through high-resolution transmission electron microscopy, infrared/Raman spectroscopy, and X-ray diffraction indicate that abundant small oxygenous graphite domains existed and endowed the HFCNs with fluorescent properties. After simple post-treatments, the cross-linked HFCNs can be used for cell-imaging applications. Compared with traditional dyes and CdTe quantum dots, HFCNs are the superior fluorescent bioimaging agent according to their low toxicity, stability, and resistance to photobleaching. The HFCNs were also applied to watermark ink and fluorescent powder, showing their promising potentials for further wide usage. PMID:22188541

  6. Gold nanoparticles grown inside carbon nanotubes: synthesis and electrical transport measurements

    Science.gov (United States)

    2014-01-01

    The hybrid structures composed of gold nanoparticles and carbon nanotubes were prepared using porous alumina membranes as templates. Carbon nanotubes were synthesized inside the pores of these templates by the non-catalytic decomposition of acetylene. The inner cavity of the supported tubes was used as nanoreactors to grow gold particles by impregnation with a gold salt, followed by a calcination-reduction process. The samples were characterized by transmission electron microscopy and X-ray energy dispersion spectroscopy techniques. The resulting hybrid products are mainly encapsulated gold nanoparticles with different shapes and dimensions depending on the concentration of the gold precursor and the impregnation procedure. In order to understand the electronic transport mechanisms in these nanostructures, their conductance was measured as a function of temperature. The samples exhibit a ‘non-metallic’ temperature dependence where the dominant electron transport mechanism is 1D hopping. Depending on the impregnation procedure, the inclusion of gold nanoparticles inside the CNTs can introduce significant changes in the structure of the tubes and the mechanisms for electronic transport. The electrical resistance of these hybrid structures was monitored under different gas atmospheres at ambient pressure. Using this hybrid nanostructures, small amounts of acetylene and hydrogen were detected with an increased sensibility compared with pristine carbon nanotubes. Although the sensitivity of these hybrid nanostructures is rather low compared to alternative sensing elements, their response is remarkably fast under changing gas atmospheres. PMID:24910571

  7. Direct synthesis of mesostructured carbon nanofibers decorated with silver-nanoparticles as a multifunctional membrane for water treatment

    Science.gov (United States)

    Aboueloyoun Taha, Ahmed

    2015-12-01

    One-dimensional (1D) porous carbon nanofibers (CNFs) decorated by silver (Ag) nanoparticles (NPs) were prepared using a one-pot/self-template synthesis strategy by combining electrospinning and carbonization methods. The characterization results revealed that AgNPs were homogenously distributed along the CNFs and possessed a relatively uniform nano-size of about 12 nm. The novel membrane distinctively displayed enhanced photocatalytic activity under visible-light irradiation. The membrane exhibited excellent dye degradation and bacteria disinfection in batch experiments. The high photocatalytic activity can be attributed to the highly accessible surface areas, good light absorption capability, and high separation efficiency of photogenerated electron-hole pairs. The as-prepared membranes can be easily recycled because of their 1D property.

  8. Green synthesis of carbon-supported nanoparticle catalysts by physical vapor deposition on soluble powder substrates

    Science.gov (United States)

    Park, Hee-Young; Jang, Injoon; Jung, Namgee; Chung, Young-Hoon; Ryu, Jae Yoon; Cha, In Young; Kim, Hyung Juhn; Jang, Jong Hyung; Yoo, Sung Jong

    2015-09-01

    Metal and metal oxide nanoparticles (NPs) supported on high surface area carbon (NP/Cs) were prepared by the physical vapor deposition of bulk materials on an α-D-glucose (Glu) substrate, followed by the deposition of the NPs on carbon supports. Using Glu as a carrier for the transport of NPs from the bulk materials to the carbon support surfaces, ultrafine NPs were obtained, exhibiting a stabilizing effect through OH moieties on the Glu surfaces. This stabilizing effect was strong enough to stabilize the NPs, but weak enough to not significantly block the metal surfaces. As only the target materials and Glu are required in our procedure, it can be considered environmentally friendly, with the NPs being devoid of hazardous chemicals. Furthermore, the resulting NP/Cs exhibited an improvement in activity for various electrochemical reactions, mainly attributed to their high surface area.

  9. Synthesis of finely divided molybdenum sulfide nanoparticles in propylene carbonate solution

    International Nuclear Information System (INIS)

    Molybdenum sulfide nanoparticles have been prepared from the reflux solution reaction involving ammonium heptamolybdate and elemental sulfur in propylene carbonate. Addition to the reaction mixture of starch as a natural capping agent leads to lesser agglomeration and smaller size of the particles. Nanoparticles of MoSx (x≈4) of 10–30 nm size are highly divided and form stable colloidal suspensions in organic solvents. Mo K edge EXAFS of the amorphous materials shows rapid exchange of oxygen to sulfur in the molybdenum coordination sphere during the solution reaction. Thermal treatment of the amorphous sulfides MoSx under nitrogen or hydrogen flow at 400 °C allows obtaining mesoporous MoS2 materials with very high pore volume and specific surface area, up to 0.45 cm3/g and 190 m2/g, respectively. The new materials show good potential for the application as unsupported hydrotreating catalysts. - Graphical abstract: Solution reaction in propylene carbonate allows preparing weakly agglomerated molybdenum sulfide with particle size 20 nm and advantageous catalytic properties. - Highlights: • Solution reaction in propylene carbonate yields MoSx particles near 20 nm size. • Addition of starch as capping agent reduces particles size and hinder agglomeration. • EXAFS at Mo K edge shows rapid oxygen to sulfur exchange in the solution. • Thermal treatment leads to MoS2 with very high porosity and surface area

  10. Phase-controlled synthesis of α-NiS nanoparticles confined in carbon nanorods for High Performance Supercapacitors

    Science.gov (United States)

    Sun, Chencheng; Ma, Mingze; Yang, Jun; Zhang, Yufei; Chen, Peng; Huang, Wei; Dong, Xiaochen

    2014-11-01

    A facile and phase-controlled synthesis of α-NiS nanoparticles (NPs) embedded in carbon nanorods (CRs) is reported by in-situ sulfurating the preformed Ni/CRs. The nanopore confinement by the carbon matrix is essential for the formation of α-NiS and preventing its transition to β-phase, which is in strong contrast to large aggregated β-NiS particles grown freely without the confinement of CRs. When used as electrochemical electrode, the hybrid electrochemical charge storage of the ultrasmall α-NiS nanoparticels dispersed in CRs is benefit for the high capacitor (1092, 946, 835, 740 F g-1 at current densities of 1, 2, 5, 10 A g-1, respectively.). While the high electrochemical stability (approximately 100% retention of specific capacitance after 2000 charge/discharge cycles) is attributed to the supercapacitor-battery electrode, which makes synergistic effect of capacitor (CRs) and battery (NiS NPs) components rather than a merely additive composite. This work not only suggests a general approach for phase-controlled synthesis of nickel sulfide but also opens the door to the rational design and fabrication of novel nickel-based/carbon hybrid supercapacitor-battery electrode materials.

  11. Facile and Green Synthesis of Palladium Nanoparticles-Graphene-Carbon Nanotube Material with High Catalytic Activity

    OpenAIRE

    Tai Sun; Zheye Zhang; Junwu Xiao; Chen Chen; Fei Xiao; Shuai Wang; Yunqi Liu

    2013-01-01

    We report a facile and green method to synthesize a new type of catalyst by coating Pd nanoparticles (NPs) on reduced graphene oxide (rGO)-carbon nanotube (CNT) nanocomposite. An rGO–CNT nanocomposite with three-dimensional microstructures was obtained by hydrothermal treatment of an aqueous dispersion of graphene oxide (GO) and CNTs. After the rGO–CNT composites have been dipped in K2PdCl4 solution, the spontaneous redox reaction between the GO–CNT and PdCl4 2− led to the formation of nanohy...

  12. Strings of interconnected hollow carbon nanoparticles with porous shells prepared using simple solid-phase synthesis

    International Nuclear Information System (INIS)

    Strings of interconnected hollow carbon nanoparticles with porous shells were prepared by simple heat-treatments of a mixture of resorcinol-formaldehyde gel and transition-metal salts. The sample was characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction and nitrogen adsorption. Results show that the sample consisted of relatively uniform hollow particles with sizes ranging from 70 to 80 nm forming a strings-of-pearls-like nanostructure. The material with porous shells possessed well-developed graphitic structure with an interlayer (d002) spacing of 0.3369 nm and the stack height of the graphite crystallites of 9 nm

  13. 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.

  14. Electrochemical synthesis of elongated noble metal nanoparticles, such as nanowires and nanorods, on high-surface area carbon supports

    Energy Technology Data Exchange (ETDEWEB)

    Adzic, Radoslav; Blyznakov, Stoyan; Vukmirovic, Miomir

    2015-08-04

    Elongated noble-metal nanoparticles and methods for their manufacture are disclosed. The method involves the formation of a plurality of elongated noble-metal nanoparticles by electrochemical deposition of the noble metal on a high surface area carbon support, such as carbon nanoparticles. Prior to electrochemical deposition, the carbon support may be functionalized by oxidation, thus making the manufacturing process simple and cost-effective. The generated elongated nanoparticles are covalently bound to the carbon support and can be used directly in electrocatalysis. The process provides elongated noble-metal nanoparticles with high catalytic activities and improved durability in combination with high catalyst utilization since the nanoparticles are deposited and covalently bound to the carbon support in their final position and will not change in forming an electrode assembly.

  15. In situ synthesis and modification of calcium carbonate nanoparticles via a bobbling method

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Modified calcium carbonate (CaCO3) nanoparticles with cubic- and spindle-like configuration were synthesized in situ by the typical bobbling (gas-liquid-solid) method. The modifiers, such as sodium stearate, octadecyl dihydrogen phosphate (ODP) and oleic acid (OA), were used to obtain hydrophobic nanoparticles. The different modification effects of the modifiers were investigated by measuring the active ratio, whiteness and the contact angle. Moreover, transmission electron microscopy (TEM), X-ray diffraction (XRD) and thermogravimetry analysis (TGA analysis) were employed to characterize the obtained products. A preliminary reaction mechanism was discussed. According to the results, the active ratio of CaCO3 modified by ODP was ca. 99.9% and the value of whiteness was 97.3% when the dosage of modifiers reached 2%. The contact angle was 122.25° for the CaCO3 modified in the presence of sodium stearate, ODP and OA. When modified CaCO3 was filled into PVC, the mechanical properties of products were improved greatly such as rupture intensity, pull intensity and fuse temperature. The compatibility and affinity between the modified CaCO3 nanoparticles and the organic matrixes were greatly improved.

  16. Synthesis of Fe3O4/Pt Nanoparticles Decorated Carbon Nanotubes and Their Use as Magnetically Recyclable Catalysts

    Directory of Open Access Journals (Sweden)

    Hongkun He

    2011-01-01

    Full Text Available We report a facile approach to prepare Fe3O4/Pt nanoparticles decorated carbon nanotubes (CNTs. The superparamagnetic Fe3O4 nanoparticles with average size of 4∼5 nm were loaded on the surfaces of carboxyl groups functionalized CNTs via a high-temperature solution-phase hydrolysis method from the raw material of FeCl3. The synthesis process of magnetic CNTs is green and readily scalable. The loading amounts of Fe3O4 nanopartilces and the magnetizations of the resulting magnetic CNTs show good tunability. The Pt nanopaticles with average size of 2.5 nm were deposited on the magnetic CNTs through a solution-based method. It is demonstrated that the Fe3O4/Pt nanoparticles decorated CNTs have high catalytic activity in the reduction reaction of 4-nitrophenol and can be readily recycled by a magnet and reused in the next reactions with high efficiencies for at least fifteen successive cycles. The novel CNTs-supported magnetically recyclable catalysts are promising in heterogeneous catalysis applications.

  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. Synthesis and Capacitive Properties of Manganese Oxide Nanoparticles Dispersed on Hierarchical Porous Carbons

    International Nuclear Information System (INIS)

    Graphical abstract: Display Omitted - Highlights: • By contrast with template methods, HPCs are obtained by activation of humic acid, which is simple and cost-effective. • HPCs are rich in oxygen-containing functional groups, which allow the formation and uniform anchoring of fine MnO2 via strong chemical interactions between the functional groups of HPCs and the nanomaterials. - Abstract: A growing manganese dioxide (MnO2) nanoparticles on hierarchical porous carbons (HPCs) is conducted via a simple route starting with KMnO4 and ethanol aimed to enhance the electrochemically active surface area of MnO2. It is found that these MnO2 nanoparticles are uniformly grown on the external surface of the HPCs and still maintain hierarchical porous structure, yielding a composite electrode showing good electron transport, rapid ion penetration, fast and reversible Faradic reaction when used as supercapacitor electrode materials. HPCs–MnO2 composite displays the specific capacitance as high as 167 F g−1 and 192 F cm−3 in 3 M KOH aqueous electrolyte and 94 F g−1 and 113 F cm−3 in 1 M tetraethylammonium tetrafluoroborate/propylene carbonate (Et4NBF4/PC) organic electrolyte. Furthermore, it also exhibits a superior cycling stability with 96% retention of the initial specific capacitance after 1000 cycles and stable Coulombic efficiency of 99% in 3 M KOH measured using the galvanostatic charge–discharge technique

  19. Synthesis of agarose-metal/semiconductor nanoparticles having superior bacteriocidal activity and their simple conversion to metal-carbon composites

    Indian Academy of Sciences (India)

    K K R Datta; B Srinivasan; H Balaram; M Eswaramoorthy

    2008-11-01

    Agarose, a naturally occurring biopolymer is used for the stabilization of metal, semiconductor nanoparticles. Ag and Cu nanoparticles stabilized in agarose matrix show excellent antibacterial activity against E. coli bacteria. The well dispersed metal nanoparticles within the agarose composite films can be readily converted to carbon-metal composites of catalytic importance.

  20. 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.

  1. Ni–Mo and Co–Mo alloy nanoparticles for catalytic chemical vapor deposition synthesis of carbon nanotubes

    International Nuclear Information System (INIS)

    Highlights: • Thermal decomposition of the ε-Keggin-type polyoxomolybdate clusters Mo12O28(μ2-OH)12{Ni(H2O)3}4 and Mo12O28(μ2-OH)12{Co(H2O)3}4 produces NiMoO4 and CoMoO4 phases. • The NiMoO4 and CoMoO4 phases are converted in alloys with a metal ratio of 1:1. • The Ni–Mo and Co–Mo alloy nanoparticles catalyze a CCVD growth of carbon nanotubes. - Abstract: Here, we show for the first time a catalytic chemical vapor deposition (CCVD) synthesis of carbon nanotubes (CNTs) using polyoxomolybdate clusters Mo12O28(μ2-OH)12{Ni(H2O)3}4 and Mo12O28(μ2-OH)12{Co(H2O)3}4 as a source of catalyst nanoparticles. X-ray diffraction analyses indicated that the products of thermal decomposition of the clusters contain NiMoO4 and CoMoO4 phases, which are converted into Ni–Mo and Co–Mo alloys at 900 °C in hydrogen environment. High-resolution transmission electron microscopy in combination with energy-dispersive X-ray spectroscopy confirmed the CNT growth from bimetallic nanoparticles. Synergism between two metals in an alloy resulted in large-scale production of non-bundled few-walled CNTs with narrow diameter distribution and high quality

  2. Controllable synthesis and characterization of novel copper-carbon core-shell structured nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhai, Jing [Sin-China Nano Technology Center, Key Lab for Nanomaterials, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Research Center of the Ministry of Education for High Gravity Engineering and Technology, Beijing University of Chemical Technology, No. 15 Beisanhuan Dong Lu, Beijing 100029 (China); Tao, Xia; Pu, Yuan; Zeng, Xiao-Fei [Sin-China Nano Technology Center, Key Lab for Nanomaterials, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Chen, Jian-Feng, E-mail: chenjf@mail.buct.edu.cn [Research Center of the Ministry of Education for High Gravity Engineering and Technology, Beijing University of Chemical Technology, No. 15 Beisanhuan Dong Lu, Beijing 100029 (China)

    2011-06-15

    Highlights: {yields} We reported a facile, green and cheap hydrothermal method to obtain novel copper-carbon core-shell nanoparticles. {yields} The as-formed particles with controllable size and morphology are antioxidant. {yields} The particles with organic-group-loaded surfaces and protective shells are expected to be applied in fields of medicine, electronics, sensors and lubricant. -- Abstract: A facile hydrothermal method was developed for preparing copper-carbon core-shell structured particles through a reaction at 160 {sup o}C in which glucose, copper sulfate pentahydrate and cetyltrimethylammonium bromide were used as starting materials. The original copper-carbon core-shell structured particles obtained were sized of 100-250 nm. The thickness of carbonaceous shells was controlled ranging from 25 to 100 nm by adjusting the hydrothermal duration time and the concentrations of glucose in the process. Products were characterized with transmission electron microscopy, X-ray diffraction, energy dispersive spectroscopy, Fourier transform infrared spectroscopy. Since no toxic materials were involved in the preparation, particles with stable carbonaceous framework and reactive surface also showed promising applications in medicine, electronics, sensors, lubricant, etc.

  3. Controllable synthesis and characterization of novel copper-carbon core-shell structured nanoparticles

    International Nuclear Information System (INIS)

    Highlights: → We reported a facile, green and cheap hydrothermal method to obtain novel copper-carbon core-shell nanoparticles. → The as-formed particles with controllable size and morphology are antioxidant. → The particles with organic-group-loaded surfaces and protective shells are expected to be applied in fields of medicine, electronics, sensors and lubricant. -- Abstract: A facile hydrothermal method was developed for preparing copper-carbon core-shell structured particles through a reaction at 160 oC in which glucose, copper sulfate pentahydrate and cetyltrimethylammonium bromide were used as starting materials. The original copper-carbon core-shell structured particles obtained were sized of 100-250 nm. The thickness of carbonaceous shells was controlled ranging from 25 to 100 nm by adjusting the hydrothermal duration time and the concentrations of glucose in the process. Products were characterized with transmission electron microscopy, X-ray diffraction, energy dispersive spectroscopy, Fourier transform infrared spectroscopy. Since no toxic materials were involved in the preparation, particles with stable carbonaceous framework and reactive surface also showed promising applications in medicine, electronics, sensors, lubricant, etc.

  4. Synthesis and Photocatalytic Activity of Anatase TiO2 Nanoparticles-coated Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Xie Yi

    2009-01-01

    Full Text Available Abstract A simple and straightforward approach to prepare TiO2-coated carbon nanotubes (CNTs is presented. Anatase TiO2 nanoparticles (NPs with the average size ~8 nm were coated on CNTs from peroxo titanic acid (PTA precursor even at low temperature of 100 °C. We demonstrate the effects of CNTs/TiO2 molar ratio on the adsorption capability and photocatalytic efficiency under UV–visible irradiation. The samples showed not only good optical absorption in visible range, but also great adsorption capacity for methyl orange (MO dye molecules. These properties facilitated the great enhancement of photocatalytic activity of TiO2 NPs-coated CNTs photocatalysts. The TiO2 NPs-coated CNTs exhibited 2.45 times higher photocatalytic activity for MO degradation than that of pure TiO2.

  5. Synthesis of carbon-supported PtRh random alloy nanoparticles using electron beam irradiation reduction method

    Science.gov (United States)

    Matsuura, Yoshiyuki; Seino, Satoshi; Okazaki, Tomohisa; Akita, Tomoki; Nakagawa, Takashi; Yamamoto, Takao A.

    2016-05-01

    Bimetallic nanoparticle catalysts of PtRh supported on carbon were synthesized using an electron beam irradiation reduction method. The PtRh nanoparticle catalysts were composed of particles 2-3 nm in size, which were well dispersed on the surface of the carbon support nanoparticles. Analyses of X-ray diffraction and scanning transmission electron microscopy-energy-dispersive X-ray spectroscopy revealed that the PtRh nanoparticles have a randomly alloyed structure. The lattice constant of the PtRh nanoparticles showed good correlation with Vegard's law. These results are explained by the radiochemical formation process of the PtRh nanoparticles. Catalytic activities of PtRh/C nanoparticles for ethanol oxidation reaction were found to be higher than those obtained with Pt/C.

  6. 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.

  7. Dense medium plasma synthesis of carbon/iron-based magnetic nanoparticle system

    International Nuclear Information System (INIS)

    Using dense medium plasma technology, hybrid iron and iron oxide/carbon-based nanoparticle composites were synthesized under room temperature and atmospheric pressure conditions. Based on results from electron spectroscopy for chemical analysis, Fourier transform infrared spectroscopy, Raman microscopy, atomic force microscopy and scanning electron microscopy, we conclude that the material is composed of spherical particles, 40-60 nm in diameter, which are a graphitic carbon host structure embedded with iron and iron oxide. Thermal gravimetry/differential thermal gravimetry analysis indicates that these composites are stable up to temperatures as high as 600 deg. C. Ferromagnetic resonance spectroscopy (FMR) and extended x-ray absorption fine-structure spectroscopy suggest that the bulk of the FMR signal in question is due to metallic Fe. Magnetite or maghemite is present, and the metallic content of the metal particles is 58(8)% and the remainder is oxidized with a sixfold oxygen coordination shell similar to that of γ-Fe2O3

  8. Modern Approach to the Synthesis of Ni(OH)2 Decorated Sulfur Doped Carbon Nanoparticles for the Nonenzymatic Glucose Sensor.

    Science.gov (United States)

    Karikalan, Natarajan; Velmurugan, Murugan; Chen, Shen-Ming; Karuppiah, Chelladurai

    2016-08-31

    As a growing aspect of materials science, there are an enormous number of synthesis routes that have been identified to produce materials, particularly through simple methodologies. In this way, the present study focuses on the easiest way to prepare sulfur doped carbon nanoparticles (SDCNs) using a flame synthesis method and has also demonstrated a novel route to synthesize Ni(OH)2 decorated SDCNs by a simple adsorption cum precipitation method. The SDCNs are alternative candidates to prestigious carbon materials such as graphene, carbon nanotubes, and fullerenes. Moreover, SDCNs provide excellent support to the Ni(2+) ion adsorption and initiate the formation of Ni(OH)2. The formation of Ni(OH)2 on the SDCN matrix was confirmed by Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), selected area diffraction pattern (SAED), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). After these meticulous structural evaluations, we have described the mechanism for the formation of Ni(OH)2 on an SDCN matrix. The as-prepared Ni(OH)2 decorated SDCN nanocomposites were used as an electrode material for nonenzymatic glucose sensors. The fabricated glucose sensor exhibited a wide linear concentration range, 0.0001-5.22 mM and 5.22-10.22 mM, and a low-level detection limit of 28 nM. Additionally, it reveals excellent selectivity in the potentially interfering ions and also possesses a good stability. The practicality of the fabricated glucose sensor was also demonstrated toward glucose detection in biological samples. PMID:27519122

  9. Unifying the templating effects of porous anodic alumina on metallic nanoparticles for carbon nanotube synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Haase, Mark R., E-mail: Mark.R.Haase@gmail.com, E-mail: haasemr@mail.uc.edu; Alvarez, Noe T.; Malik, Rachit; Schulz, Mark; Shanov, Vesselin [580 Engineering Research Center, Department of Biomedical, Chemical and Environmental Engineering (United States)

    2015-09-15

    Carbon nanotubes (CNTs) are a promising material for many applications, due to their extraordinary properties. Some of these properties vary in relation to the diameter of the nanotubes; thus, precise control of CNT diameter can be critical. Porous anodic alumina (PAA) membranes have been successfully used to template electrodeposited catalyst. However, the catalysts used in CNT synthesis are frequently deposited with more precise techniques, such as electron beam deposition. We test the efficacy of PAA as a template for electron beam-deposited catalyst by studying the diameter distribution of CNTs grown catalyst of various thicknesses supported by PAA. These are then compared by ANOVA to the diameter distributions of CNTs grown on metal catalyst supported by a conventional alumina film. These results also allow a unified description of two templating effects, the more common particles-in-pores model, and the recently described particles-between-pores.

  10. Synthesis of carbon-encapsulated iron carbide/iron nanoparticles from phenolic-formaldehyde resin and ferric nitrate

    International Nuclear Information System (INIS)

    Carbon-encapsulated iron carbide/iron nanoparticles have been synthesized on a large scale by the heat treatment of thermal plastic phenolic-formaldehyde resin with the aid of ferric nitrate. The effects of heating temperature on the morphologies and structures of carbonized products were investigated using transmission electron microscope, high-resolution transmission electron microscope and X-ray diffraction measurements. The products with diameter distribution of 20-100 nm consisted mainly of spheroidal nanoparticles separated by hollow onion-like carbon nanoparticles.

  11. Synthesis of few-walled carbon nanotube-Rh nanoparticles by arc discharge: Effect of selective oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Yanfeng, E-mail: zyfshu@gmail.com

    2012-06-15

    Highly crystalline rhodium (Rh) nanoparticles supported on carbon nanotubes were prepared by selective oxidation method. Carbon nanotubes and FeRh nanoparticles were simultaneously generated in hydrogen arc plasma. The as-grown nanomaterials can be purified by heat treatment in open air and by soaking in HCl. X-ray diffraction and selected area electron diffraction results reveal that as-grown FeRh nanoparticles have a typical chemical CsCl-type structure which can be transformed into a face-centered cubic structure by thermal annealing in the purification process. The purification process is selective toward the removal of the amorphous carbon coating the nanoparticles, and transforms Fe to Fe{sub 2}O{sub 3}. Fe{sub 2}O{sub 3} can be easily dissolved in hydrochloric acid, leaving carbon nanotubes-Rh nanoparticles. Rh nanoparticles with diameters of 2-60 nm are deposited uniformly on the surface of the carbon nanotube bundles. This simple and selective chemistry offers a new process for synthesizing and controlling Fe content in carbon nanotube-FeRh nanoparticles. Highlights: Black-Right-Pointing-Pointer High-crystallinity CNTs and FeRh nanoparticles were simultaneously generated in arc plasma. Black-Right-Pointing-Pointer The diameter distribution of CNTs depends on different gases. Black-Right-Pointing-Pointer Heat treatment in open air and soaking in HCl can convert CNTs-FeRh to CNTs-Rh. Black-Right-Pointing-Pointer The selective oxidation mechanisms of metal nanoparticles and carbon materials differ.

  12. Facile and Green Synthesis of Palladium Nanoparticles-Graphene-Carbon Nanotube Material with High Catalytic Activity

    Science.gov (United States)

    Sun, Tai; Zhang, Zheye; Xiao, Junwu; Chen, Chen; Xiao, Fei; Wang, Shuai; Liu, Yunqi

    2013-08-01

    We report a facile and green method to synthesize a new type of catalyst by coating Pd nanoparticles (NPs) on reduced graphene oxide (rGO)-carbon nanotube (CNT) nanocomposite. An rGO-CNT nanocomposite with three-dimensional microstructures was obtained by hydrothermal treatment of an aqueous dispersion of graphene oxide (GO) and CNTs. After the rGO-CNT composites have been dipped in K2PdCl4 solution, the spontaneous redox reaction between the GO-CNT and PdCl42- led to the formation of nanohybrid materials consisting rGO-CNT decorated with 4 nm Pd NPs, which exhibited excellent and stable catalytic activity: the reduction of 4-nitrophenol to 4-aminophenol using NaBH4 as a catalyst was completed in only 20 s at room temperature, even when the Pd content of the catalyst was 1.12 wt%. This method does not require rigorous conditions or toxic agents and thus is a rapid, efficient, and green approach to the fabrication of highly active catalysts.

  13. CaCO3 nanoparticle synthesis by carbonation of lime solution in microemulsion systems

    NARCIS (Netherlands)

    Sugih, A.K.; Shukla, D.; Heeres, H.J.; Mehra, A.

    2007-01-01

    Various aspects of nanoparticle precipitation in gas-reverse micellar systems have been studied. The experimental system chosen for investigation deals with the precipitation of CaCO3 nanoparticles. The effect of operating variables, such as water-to-surfactant molar ratio, different continuous phas

  14. Bimetallic CuCo nanoparticles derived from hydrotalcite supported on carbon fibers for higher alcohols synthesis from syngas

    Science.gov (United States)

    Wang, Lianfang; Cao, Ang; Liu, Guilong; Zhang, Lihong; Liu, Yuan

    2016-01-01

    Higher alcohols synthesis (HAS) is a strong exothermal reaction which leads to the formation of hotspots on the catalysts and the hotspots result in poor selectivity, and Cu-Co based catalysts are one of the most promising to which the formation of Cu-Co alloy is critical. Therefore a new scheme was proposed, based on the excellent thermal conductivity of carbon fibers (CFs) and the uniform mixing of metal ions in layered double hydroxides (LDHs), the latter favors the formation of metallic alloy. Nanocomposites of LDHs and CFs were prepared by using co-precipitation method and used for HAS, and characterized by using FTIR, N2 adsorption-desorption, XRD, TPR, SEM and TEM techniques. In the composites, nanosheets with the typical LDHs morphology are perpendicularly grown on the surface of CFs while intersecting each other, creating a highly open and porous structure. After reduction, Cu-Co-alloy nanoparticles are formed from the LDHs. The resultant catalysts showed high activity and much high selectivity to higher alcohols. The reported methods can be expanded to prepare other LDHs/CFs composites.

  15. Chemical Synthesis of Copper Nanoparticles

    Directory of Open Access Journals (Sweden)

    Hamid Reza Ghorbani

    2014-06-01

    Full Text Available Metal nanoparticles have attracted considerable interest particularly because of the size dependence of physical and chemical properties and its enormous technological potential. Among different metal nanoparticles, copper nanoparticles have attracted great attention because copper is one of the most key metals in new technology. Chemical methods are used to synthesize copper nanoparticles and among them chemical reduction is the most frequently applied method for the preparation of stable, colloidal dispersions in organic solvents. In this paper, a brief overview of the current research worldwide in the chemical synthesis of copper nanoparticles is discussed.

  16. Diamond Synthesis Employing Nanoparticle Seeds

    Science.gov (United States)

    Uppireddi, Kishore (Inventor); Morell, Gerardo (Inventor); Weiner, Brad R. (Inventor)

    2014-01-01

    Iron nanoparticles were employed to induce the synthesis of diamond on molybdenum, silicon, and quartz substrates. Diamond films were grown using conventional conditions for diamond synthesis by hot filament chemical vapor deposition, except that dispersed iron oxide nanoparticles replaced the seeding. This approach to diamond induction can be combined with dip pen nanolithography for the selective deposition of diamond and diamond patterning while avoiding surface damage associated to diamond-seeding methods.

  17. Synthesis of Nanoscale Heterostructures Comprised of Metal Nanowires, Carbon Nanotubes, and Metal Nanoparticles: Investigation of Their Structure and Electrochemical Properties

    Directory of Open Access Journals (Sweden)

    Nitin Chopra

    2015-01-01

    Full Text Available One-dimensional nanoscale heterostructures comprised of multisegment gold-nickel nanowires, carbon nanotube, and nickel nanoparticles were fabricated in a unique approach combining top-down and bottom-up assembly methods. Porous alumina template was utilized for sequential electrodeposition of gold and nickel nanowire segments. This was followed by chemical vapor deposition growth of carbon nanotubes on multisegment gold-nickel nanowires, where nickel segment also acted as a carbon nanotube growth catalyst. The aligned arrays of these gold-nickel-carbon nanotube heterostructures were released from porous alumina template and then subjected to wet-chemical process to be decorated with nickel/nickel oxide core/shell nanoparticles. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy were utilized for morphology, interface, defect, and structure characterization. The electrochemical performance of these heterostructures was studied using cyclic voltammetry method and the specific capacitance of various heterostructures was estimated and compared.

  18. Multicomponent click synthesis of potentially biologically active triazoles catalysed by copper nanoparticles on activated carbon in water

    OpenAIRE

    Alonso Valdés, Francisco; Moglie, Yanina; Radivoy, Gabriel; Yus Astiz, Miguel

    2011-01-01

    A variety of potentially biologically active 1,2,3-triazoles, derived from (–)-menthol, lactic acid, D-glucose, oestrone, cholesterol, and phenacetin, have been synthesised through the multicomponent alkyne-azide 1,3-dipolar cycloaddition catalysed by copper nanoparticles on activated carbon in neat water.

  19. Synthesis of TiO2 nanoparticles containing Fe, Si, and V using multiple diffusion flames and catalytic oxidation capability of carbon-coated nanoparticles

    KAUST Repository

    Ismail, Mohamed

    2016-01-19

    Titanium dioxide (TiO2) nanoparticles containing iron, silicon, and vanadium are synthesized using multiple diffusion flames. The growth of carbon-coated (C–TiO2), carbon-coated with iron oxide (Fe/C–TiO2), silica-coated (Si–TiO2), and vanadium-doped (V–TiO2) TiO2 nanoparticles is demonstrated using a single-step process. Hydrogen, oxygen, and argon are utilized to establish the flame, with titanium tetraisopropoxide (TTIP) as the precursor for TiO2. For the growth of Fe/C–TiO2 nanoparticles, TTIP is mixed with xylene and ferrocene. While for the growth of Si–TiO2 and V–TiO2, TTIP is mixed with hexamethyldisiloxane (HMDSO) and vanadium (V) oxytriisopropoxide, respectively. The synthesized nanoparticles are characterized using high-resolution transmission electron microscopy (HRTEM) with energy-filtered TEM for elemental mapping (of Si, C, O, and Ti), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), nitrogen adsorption BET surface area analysis, and thermogravimetric analysis. Anatase is the dominant phase for the C–TiO2, Fe/C–TiO2, and Si–TiO2 nanoparticles, whereas rutile is the dominant phase for the V–TiO2 nanoparticles. For C–TiO2 and Fe/C–TiO2, the nanoparticles are coated with about 3-5-nm thickness of carbon. The iron-based TiO2 nanoparticles significantly improve the catalytic oxidation of carbon, where complete oxidation of carbon occurs at a temperature of 470 °C (with iron) compared to 610 °C (without iron). Enhanced catalytic oxidation properties are also observed for model soot particles, Printex-U, when mixed with Fe/C-TiO2. With regards to Si–TiO2 nanoparticles, a uniform coating of 3 to 8 nm of silicon dioxide is observed around the TiO2 particles. This coating mainly occurs due to variance in the chemical reaction rates of the precursors. Finally, with regards to V–TiO2, vanadium is doped within the TiO2 nanoparticles as visualized by HRTEM and XPS further confirms the formation of

  20. Synthesis of TiO{sub 2} nanoparticles containing Fe, Si, and V using multiple diffusion flames and catalytic oxidation capability of carbon-coated nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ismail, Mohamed A. [King Abdullah University of Science and Technology (KAUST), Clean Combustion Research Center (Saudi Arabia); Memon, Nasir K., E-mail: nmemon@qf.org.qa [HBKU, Qatar Foundation, Qatar Environment and Energy Research Institute (QEERI) (Qatar); Hedhili, Mohamed N.; Anjum, Dalaver H. [KAUST, Imaging and Characterization Lab (Saudi Arabia); Chung, Suk Ho [King Abdullah University of Science and Technology (KAUST), Clean Combustion Research Center (Saudi Arabia)

    2016-01-15

    Titanium dioxide (TiO{sub 2}) nanoparticles containing iron, silicon, and vanadium are synthesized using multiple diffusion flames. The growth of carbon-coated (C–TiO{sub 2}), carbon-coated with iron oxide (Fe/C–TiO{sub 2}), silica-coated (Si–TiO{sub 2}), and vanadium-doped (V–TiO{sub 2}) TiO{sub 2} nanoparticles is demonstrated using a single-step process. Hydrogen, oxygen, and argon are utilized to establish the flame, with titanium tetraisopropoxide (TTIP) as the precursor for TiO{sub 2}. For the growth of Fe/C–TiO{sub 2} nanoparticles, TTIP is mixed with xylene and ferrocene. While for the growth of Si–TiO{sub 2} and V–TiO{sub 2}, TTIP is mixed with hexamethyldisiloxane (HMDSO) and vanadium (V) oxytriisopropoxide, respectively. The synthesized nanoparticles are characterized using high-resolution transmission electron microscopy (HRTEM) with energy-filtered TEM for elemental mapping (of Si, C, O, and Ti), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), nitrogen adsorption BET surface area analysis, and thermogravimetric analysis. Anatase is the dominant phase for the C–TiO{sub 2}, Fe/C–TiO{sub 2}, and Si–TiO{sub 2} nanoparticles, whereas rutile is the dominant phase for the V–TiO{sub 2} nanoparticles. For C–TiO{sub 2} and Fe/C–TiO{sub 2}, the nanoparticles are coated with about 3-5-nm thickness of carbon. The iron-based TiO{sub 2} nanoparticles significantly improve the catalytic oxidation of carbon, where complete oxidation of carbon occurs at a temperature of 470 °C (with iron) compared to 610 °C (without iron). Enhanced catalytic oxidation properties are also observed for model soot particles, Printex-U, when mixed with Fe/C-TiO{sub 2}. With regards to Si–TiO{sub 2} nanoparticles, a uniform coating of 3 to 8 nm of silicon dioxide is observed around the TiO{sub 2} particles. This coating mainly occurs due to variance in the chemical reaction rates of the precursors. Finally, with regards

  1. 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.

  2. 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

  3. Synthesis and mechanical behavior of carbon nanotube-magnesium composites hybridized with nanoparticles of alumina

    International Nuclear Information System (INIS)

    Carbon nanotubes reinforced magnesium based composites were prepared with diligence and care using the powder metallurgy route coupled with rapid microwave sintering. Nanometer-sized particles of alumina were used to hybridize the carbon nanotubes reinforcement in the magnesium matrix so as to establish the intrinsic influence of hybridization on mechanical behavior of the resultant composite material. The yield strength, tensile strength and strain-to-failure of the carbon nanotubes-magnesium composites were found to increase with the addition of nanometer-sized alumina particles to the composite matrix. Scanning electron microscopy observations of the fracture surfaces of the samples deformed and failed in uniaxial tension revealed the presence of cleavage-like features on the fracture surface indicative of the occurrence of locally brittle fracture mechanism in the composite microstructure

  4. Microwave-assisted synthesis and characterization of bimetallic PtRu alloy nanoparticles supported on carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Rahsepar, Mansour, E-mail: rahsepar@shirazu.ac.ir [Department of Materials Science and Engineering, School of Engineering, Shiraz University, Zand Boulevard, Shiraz, 7134851154 (Iran, Islamic Republic of); Kim, Hasuck, E-mail: hasuckim@snu.ac.kr [Department of Chemistry, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul, 151-747 (Korea, Republic of); Department of Energy Systems Engineering, Daegu Gyeongbuk Institute of Science & Technology, Daegu, 711-873 (Korea, Republic of)

    2015-11-15

    Multiwalled carbon nanotube (MWCNT) supported PtRu nanoparticles were synthesized by using a microwave-assisted improved impregnation technique. X-ray diffraction, transmission electron microscopy and X-ray photo electron spectroscopy were used to characterize the prepared PtRu/MWCNT nanoparticles. The PtRu nanoparticles with a satisfactory dispersion were formed on the external surface of MWCNTs. The CO stripping experiment was performed to evaluate the poisoning resistance of the prepared PtRu/MWCNT nanoparticles. Results of electrochemical measurements indicate that the prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning. The results of characterization revealed that microwave-assisted improved impregnation technique have a high yield of alloy phase formation and could be effectively used as a simple, quick and efficient technique for preparation of bimetallic PtRu/MWCNT nanoparticles. - Highlights: • Highly dispersed PtRu/MWCNTs were formed without use of any stabilizing agent. • Microwave irradiation enhances the uniform dispersion of the PtRu nanoparticles. • Microwave-assisted improved impregnation have a high yield of alloy phase formation. • The prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning.

  5. Microwave-assisted synthesis and characterization of bimetallic PtRu alloy nanoparticles supported on carbon nanotubes

    International Nuclear Information System (INIS)

    Multiwalled carbon nanotube (MWCNT) supported PtRu nanoparticles were synthesized by using a microwave-assisted improved impregnation technique. X-ray diffraction, transmission electron microscopy and X-ray photo electron spectroscopy were used to characterize the prepared PtRu/MWCNT nanoparticles. The PtRu nanoparticles with a satisfactory dispersion were formed on the external surface of MWCNTs. The CO stripping experiment was performed to evaluate the poisoning resistance of the prepared PtRu/MWCNT nanoparticles. Results of electrochemical measurements indicate that the prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning. The results of characterization revealed that microwave-assisted improved impregnation technique have a high yield of alloy phase formation and could be effectively used as a simple, quick and efficient technique for preparation of bimetallic PtRu/MWCNT nanoparticles. - Highlights: • Highly dispersed PtRu/MWCNTs were formed without use of any stabilizing agent. • Microwave irradiation enhances the uniform dispersion of the PtRu nanoparticles. • Microwave-assisted improved impregnation have a high yield of alloy phase formation. • The prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning

  6. Barium hexaferrite nanoparticles: Synthesis and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Martirosyan, K.S., E-mail: karen.martirosyan@utb.edu [Department of Chemical and Biomolecular Engineering, University of Houston, Houston, TX 77204 (United States); Texas Center for Superconductivity, University of Houston, Houston, TX 77204 (United States); Department of Electrical and Computer Engineering, University of Houston, Houston, TX 77204 (United States); Galstyan, E. [Texas Center for Superconductivity, University of Houston, Houston, TX 77204 (United States); Hossain, S.M.; Wang Yiju [Department of Electrical and Computer Engineering, University of Houston, Houston, TX 77204 (United States); Litvinov, D. [Department of Chemical and Biomolecular Engineering, University of Houston, Houston, TX 77204 (United States); Texas Center for Superconductivity, University of Houston, Houston, TX 77204 (United States); Department of Electrical and Computer Engineering, University of Houston, Houston, TX 77204 (United States)

    2011-01-15

    Carbon combustion synthesis is applied to rapid and energy efficient fabrication of crystalline barium hexaferrite nanoparticles with the average particle size of 50-100 nm. In this method, the exothermic oxidation of carbon nanoparticles with an average size of 5 nm with a surface area of 80 m{sup 2}/g generates a self-propagating thermal wave with maximum temperatures of up to 1000 deg. C. The thermal front rapidly propagates through the mixture of solid reactants converting it to the hexagonal barium ferrite. Carbon is not incorporated in the product and is emitted from the reaction zone as a gaseous CO{sub 2}. The activation energy for carbon combustion synthesis of BaFe{sub 12}O{sub 19} was estimated to be 98 kJ/mol. A complete conversion to hexagonal barium ferrite is obtained for carbon concentration exceeding 11 wt.%. The magnetic properties H{sub c}{approx}3000 Oe and M{sub s}{approx}50.3 emu/g of the compact sintered ferrites compare well with those produced by other synthesis methods.

  7. Barium hexaferrite nanoparticles: Synthesis and magnetic properties

    International Nuclear Information System (INIS)

    Carbon combustion synthesis is applied to rapid and energy efficient fabrication of crystalline barium hexaferrite nanoparticles with the average particle size of 50-100 nm. In this method, the exothermic oxidation of carbon nanoparticles with an average size of 5 nm with a surface area of 80 m2/g generates a self-propagating thermal wave with maximum temperatures of up to 1000 deg. C. The thermal front rapidly propagates through the mixture of solid reactants converting it to the hexagonal barium ferrite. Carbon is not incorporated in the product and is emitted from the reaction zone as a gaseous CO2. The activation energy for carbon combustion synthesis of BaFe12O19 was estimated to be 98 kJ/mol. A complete conversion to hexagonal barium ferrite is obtained for carbon concentration exceeding 11 wt.%. The magnetic properties Hc∼3000 Oe and Ms∼50.3 emu/g of the compact sintered ferrites compare well with those produced by other synthesis methods.

  8. Magnetic Carbon Nanotubes Tethered with Maghemite Nanoparticles

    Science.gov (United States)

    Kim, Il Tae; Nunnery, Grady; Jacob, Karl; Schwartz, Justin; Liu, Xiaotao; Tannenbaum, Rina

    2011-03-01

    We describe a novel, facile method for the synthesis of magnetic carbon nanotubes (m-CNTs) decorated with monodisperse γ - Fe 2 O3 magnetic (maghemite) nanoparticles and their aligned feature in a magnetic field. The tethering of the nanoparticles was achieved by the initial activation of the surface of the CNTs with carboxylic acid groups, followed by the attachment of the γ - Fe 2 O3 nanoparticles via a modified sol-gel process. Sodium dodecylbenzene sulfonate (NaDDBS) was introduced into the suspension to prevent the formation of an iron oxide 3D network. Various characterization methods were used to confirm the formation of well-defined maghemite nanoparticles. The tethered nanoparticles imparted magnetic characteristics to the CNTs, which became superparamagnetic. The m-CNTs were oriented parallel to the direction of a magnetic field. This has the potential of enhancing various properties, e.g. mechanical and electrical properties, in composite materials.

  9. Synthesis and characterization of conditioned carbon with iron nanoparticles for the arsenic removal in aqueous phase

    International Nuclear Information System (INIS)

    Using pineapple husks conditioned with carboxymethylcellulose, hexamine and ferric nitrate, a carbonaceous material was obtained with nanoparticles of Fe (C Fe), which was characterized and tested for arsenic removal in the aqueous phase. The microscopic study showed spheres 4 microns and filaments 100 nm wide, so as iron particles whose diameter decreases to an average of 38.81 nm, when pyrolysis time was increased to 180 min. their distribution in the carbonaceous matrix is homogeneous. According to energy dispersive X-ray spectroscopy, C Fe contains C (82.29%), O (7.23%), K (0.68%), Ca (3.77%) and Fe (6.25%) and its diffraction pattern shows the characteristic peak of Fe (0), which is not observed in the coal without iron. By neutron activation analysis were quantified Al, Br, Ce, Co, Cr, Cs, Eu, Hf, K, Mg, Mn, Na, Rb, Sb, Sc and Zn, they can be involved in the process of sorption of As (v) forming surface active sites. For C Fe and C B characterized by Fourier transform infrared spectrometry, groups C-H, C=O, C=C, -Nh, NH2, isocyanate and isonitrile were found, the last two were formed by the present hexamine. X-ray photoelectron spectroscopy showed energy states of C 1 and O 1 in pineapple shell washed, shell conditioned with iron, C Fe at different times and the pyrolysis coal without iron (C B). The material C Fe 180 presented a specific area of 167 m2/g and 7.12 ± 1 sites/nm2 isoelectric point while pHi = 11.1 C B is 98.80 m2/g specific area and 1.5 ± 1 sites/nm2 and pHi = 10.6, being favorable to the sorption process. The highest removal of As(v) for both materials was at ph = 2, fitting the kinetic data to pseudo-second order model. The isotherms as a function of concentration were adjusted to Freundlich model indicating multilayer chemisorption at specific sites of a heterogeneous medium. Characterization by scanning electron microscopy after the sample sorption Fe nanoparticles remain in the carbonaceous matrix being not affected by the agitation of

  10. Synthesis and magnetic properties of multiwalled carbon nanotubes decorated with magnetite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Pistone, A., E-mail: pistone@unime.it [Department of Electronic Engineering, Chemistry and Industrial Engineering, University of Messina, Messina I-98166 (Italy); Iannazzo, D.; Fazio, M. [Department of Electronic Engineering, Chemistry and Industrial Engineering, University of Messina, Messina I-98166 (Italy); Celegato, F.; Barrera, G.; Tiberto, P. [INRIM Electromagnetism Division, Torino (Italy); Giordano, A.; Azzerboni, B.; Galvagno, S. [Department of Electronic Engineering, Chemistry and Industrial Engineering, University of Messina, Messina I-98166 (Italy)

    2014-02-15

    Magnetite particles with nanoscale sizes were deposited along multiwalled carbon nanotubes (MWCNT) through a simple, effective and reproducible chemical route. The structure, morphology and magnetic properties of the hybrid materials were characterized by XRD, SEM, TEM, EDX, VSM. The characterization results show that the surface of nanotubes was loaded with iron oxides nanoclusters and each nanocluster is composed by several nanocrystals with a mean diameter of 10 nm. The experimental magnetic hysteretic behavior has been also studied by means of the Preisach model and a good agreement between experimental data and numerical computations was found.

  11. 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...

  12. 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.

  13. Synthesis of silver nanoparticles on surface-functionalized multi-walled carbon nanotubes by ultraviolet initiated photo-reduction method

    Energy Technology Data Exchange (ETDEWEB)

    Lei, Yanhua, E-mail: yhualei@gmail.com [Institute of Materials Science and Engineering, Ocean University of China, No. 238, SongLing Road Qingdao, Qingdao 266100 (China); Gao, Guanhui [Shenzhen University Town, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, No. 1068, Xueyuan Avenue, Shenzhen (China); Liu, Wechao [Institute of Materials Science and Engineering, Ocean University of China, No. 238, SongLing Road Qingdao, Qingdao 266100 (China); Liu, Tao; Yin, Yansheng [Institute of Marine Materials Science and Engineering, Shanghai Maritime University, No. 1550, LingGangXingChengHai Road Shanghai, Shanghai 201306 (China)

    2014-10-30

    Graphical abstract: - Highlights: • MWNTs decorated with Ag nanoparticle were synthesized by UV method. • No protecting or reducing agents were required. • Highly dispersed, fcc nano-Ag with diameter of 5–10 nm was formed on MWNTs. - Abstract: In this article, we described a new, facile method on fabrication of multi-walled carbon nanotubes (MWNTs) with silver nanoparticles by an ultraviolet initiated method. MWNTs were functionalized with acrylic acid to introduce carboxylic acid groups, and then the Ag nanoparticles were synthesized on the functionalized MWNTs by using of ultraviolet irradiation without adding of any protective or reductive agent. The obtained MWNTs/Ag composites were analyzed with Fourier transform infrared spectrometer (FT-IR) spectroscopy, transmission electron microscope (TEM), X-ray powder diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). It was confirmed that Ag nanoparticles with diameters in a region of 5–10 nm were anchored on the surface of MWNTs by an interaction of Ag and oxygen in the carboxyl group.

  14. Synthesis and Properties of Fe3O4-Activated Carbon Magnetic Nanoparticles for Removal of Aniline from Aqueous Solution: Equilibrium, Kinetic and Thermodynamic Studies

    Directory of Open Access Journals (Sweden)

    Babak Kakavandi

    2013-02-01

    Full Text Available In this study, powder activated carbon (PAC and magnetic nanoparticles of iron (III oxide were used for synthesis of Fe3O4-activated carbon magnetic nanoparticles (AC-Fe3O4 MNPs as an adsorbent for the removal of aniline. The characteristics of adsorbent were evaluated by SEM, TEM, XRD and BET. Also, the impact of different parameters such as pH, contact time, adsorbent dosage, aniline initials concentration and solution temperature were studied. The experimental data investigated by Langmuir and Freundlich adsorption isotherms and two models kinetically of pseudo first-order and pseudo second-order. The results indicated that the adsorption followed Langmuir and pseudo second-order models with correlation r2 > 0.98 and r2 > 0.99, respectively. The equilibrium time was obtained after 5 h. According to Langmuir model, the maximum adsorption capacity was 90.91 mg/g at pH = 6, and 20°C. The thermodynamic parameters indicated that adsorption of aniline on magnetic activated carbon was exothermic and spontaneous. This synthesized AC-Fe3O4 MNPs due to have advantages such as easy and rapid separation from solution could be applied as an adsorbent effective for removal of pollutants such as aniline from water and wastewater

  15. 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

  16. Dual Electrospray Pyrolysis for Mixed Metal Oxide (and Carbon) Composite Nanoparticle Synthesis with Applications in Energy Storage

    Science.gov (United States)

    Tang, Justin; Liu, Wen; Wang, Hailiang; Gomez, Alessandro

    We present a novel approach to synthesizing mixed metal oxide nanoparticles with a continuous, scalable aerosol flow process using the electrospray. The electrospray is a liquid atomization technique that generates a monodisperse population of highly charged liquid droplets over a broad size range (nanometric to tens of microns). Each liquid droplet serves as a micro-reactor, containing a payload of suitable precursors (such as metal nitrides), allowing for precise control over particle composition and size. By using two electrosprays of opposite polarities, the two highly charged droplets plumes are electrostatically mixed to produce a charge-neutral aerosol. Electrostatically driven droplet-droplet collisions can also be used to control morphology to some degree. This aerosol is passed through a tubular furnace via carrier gas, pyrolizing the precursors to synthesize nanomaterials. We apply this approach to manganese oxide, cobalt oxide, and carbon composite nanoparticles for use in energy storage applications.

  17. Laser oxidative pyrolysis synthesis and annealing of TiO2 nanoparticles embedded in carbon-silica shells/matrix

    Science.gov (United States)

    Fleaca, C. T.; Scarisoreanu, M.; Morjan, I.; Luculescu, C.; Niculescu, A.-M.; Badoi, A.; Vasile, E.; Kovacs, G.

    2015-05-01

    Titania nanoparticles containing a mixture of anatase and rutile phases (with mean crystalline sizes up to 24 nm) covered with/embedded in carbon/silica thin layers or matrix were obtained in a single step using laser oxidative pyrolysis. Titanium tetrachloride and hexamethyldisiloxane (HMDSO) vapors were separately introduced into the reaction zone - both together with the laser-absorbing agent (sensitizer) ethylene - which acts also as carbon source - and the oxidant (air) - through the inner and the concentric nozzle, respectively. By increasing the air flow through the annular nozzle, while keeping constant the TiC4, inner air, HMDSO and C2H4 flows, the atomic carbon concentration as well as the rutile to anatase ratio in the resulted nanopowders decrease. A much brighter and extended flame was observed for the experiment involving the greatest air flow. The Ti/Si atomic ratio in the resulted nanocomposites was higher than that from the introduced precursors (1.8), indicating a partial siloxane conversion to silica. The annealed powders (at 450 °C to further carbon content reducing) exhibit a lower bandgap energy than those of the reference sample without silica (and also lower than the commercial Degussa P25 nano-TiO2).

  18. Rapid synthesis of carbon nanoparticles with an optimized combination of specific surface area and crystallinity by a plasma-assisted single-step process

    International Nuclear Information System (INIS)

    This paper reports controlled synthesis of carbon nanoparticles by an expanded thermal plasma jet assisted technique through a single-step, high-throughput process. The plasma discharge zone in the experimental reactor remained isolated from the particle nucleation/growth chamber through a supersonic nozzle, which allowed using the sample collection chamber pressure as an efficient control parameter to synthesize carbon nanostructures with tailored combination of some important properties. Low chamber pressure conditions produced samples with both good specific surface area and crystallinity, which may be ideal for use as an efficient catalyst support material as well as in batteries and super capacitors. This dominantly mesoporous sample was also found to have good hydrogen absorption properties. Another significant observation was that the average number of carbon nano-sheets stacked together inside the crumpled paper like layers increased with pressure in the sample collection chamber. Optical emission spectroscopic techniques were used to measure the effective cooling rates responsible for the particle nucleation process under different experimental conditions, which also indicated that C2 dimer molecules are the basic precursors behind the formation of these carbon nanostructures. (paper)

  19. Chitosan-mediated synthesis of carbon nanotube-gold nanohybrids

    Institute of Scientific and Technical Information of China (English)

    GRAVEL; Edmond; FOILLARD; Stéphanie; DORIS; Eric

    2010-01-01

    Metal-nanotube nanohybrids were produced by in situ synthesis and stabilization of gold nanoparticles on chitosan-functionalized carbon nanotubes.The formation of gold nanoparticles from tetrachloroauric acid was observed after only a few minutes of contact with the functionalized nanotubes,at room temperature.These results suggest that adsorption of chitosan at the surface of carbon nanotubes permits smooth reduction of the metallic salt and efficient anchoring of gold nanoparticles to the nanotubes.

  20. 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.

  1. Red Fluorescent Carbon Nanoparticle-Based Cell Imaging Probe.

    Science.gov (United States)

    Ali, Haydar; Bhunia, Susanta Kumar; Dalal, Chumki; Jana, Nikhil R

    2016-04-13

    Fluorescent carbon nanoparticle-based probes with tunable visible emission are biocompatible, environment friendly and most suitable for various biomedical applications. However, synthesis of red fluorescent carbon nanoparticles and their transformation into functional nanoparticles are very challenging. Here we report red fluorescent carbon nanoparticle-based nanobioconjugates of carbon nanoparticles are synthesized via high temperature colloid-chemical approach and transformed into water-soluble functional nanoparticles via coating with amphiphilic polymer followed by covalent linking with desired biomolecules. Following this approach, carbon nanoparticles are functionalized with polyethylene glycol, primary amine, glucose, arginine, histidine, biotin and folic acid. These functional nanoparticles can be excited with blue/green light (i.e., 400-550 nm) to capture their emission spanning from 550 to 750 nm. Arginine and folic acid functionalized nanoparticles have been demonstrated as fluorescent cell labels where blue and green excitation has been used for imaging of labeled cells. The presented method can be extended for the development of carbon nanoparticle-based other bioimaging probes. PMID:27011336

  2. [Synthesis of Fe/nitrogen-doped Carbon Nanotube/Nanoparticle Composite and Its Catalytic Performance in Oxygen Reduction].

    Science.gov (United States)

    Yang, Ting-ting; Zhu, Neng-wu; Lu, Yu; Wu, Ping-xiao

    2016-01-15

    The cathode catalyst plays an important role in the electricity generation of microbial fuel cells (MFCs). In order to achieve the large-scale application of MFCs, cathode catalyst with low cost and high oxygen reduction reaction (ORR) has great sense to substitute the precious catalyst of Pt/C. Here chemical vapor deposition (CVD) method was utilized accompanied with melamine as a nitrogen and carbon precursor, oxidized carbon powder (Black Pearls 2000 or Acetylene Black) as carbon precursor and iron acetate as an iron precursor so as to synthesize two kinds of Fe and nitrogen doped carbon nanotube/nanoparticle composites (FeNCB and FeNCC) as MFCs cathode catalysts. The cyclic voltammetry and rotating ring-disk electrode were applied to analyze the ORR activity discrepancies of FeNCB, FeNCC, and Pt/C (20%), which was confirmed by MFC operation. The results showed that the ORR performance of FeNCB was slightly better than Pt/C and dramatically better than FeNCC. Moreover, the catalysis of ORR by FeNCB was through a four-electron transfer pathway. Besides, the performance of MFC-FeNCB was higher than MFC-Pt/C and observably higher than MFC-FeNCC which was a contribute to promote the scale of MFC. MFC-FeNCB achieved the maximum power output density of 1212.8 mW x m(-2), an open circuit potential of 0.875 V, and a stabilized voltage of (0.500 +/- 0.025) V. Further analysis via X-ray diffraction, X ray photoelectron spectroscopy, and Raman exhibited that the diameter of carbon nanotube, the types of N and Fe as well as the concentration of nitrogen, iron and oxygen was the reason for the discrepancies of ORR characteristics for the prepared catalysts. PMID:27078977

  3. Size Dependent Phase Diagrams of Nickel-Carbon Nanoparticles

    Science.gov (United States)

    Magnin, Y.; Zappelli, A.; Amara, H.; Ducastelle, F.; Bichara, C.

    2015-11-01

    The carbon rich phase diagrams of nickel-carbon nanoparticles, relevant to catalysis and catalytic chemical vapor deposition synthesis of carbon nanotubes, are calculated for system sizes up to about 3 nm (807 Ni atoms). A tight binding model for interatomic interactions drives the grand canonical Monte Carlo simulations used to locate solid, core shell and liquid stability domains, as a function of size, temperature, and carbon chemical potential or concentration. Melting is favored by carbon incorporation from the nanoparticle surface, resulting in a strong relative lowering of the eutectic temperature and a phase diagram topology different from the bulk one. This should lead to a better understanding of the nanotube growth mechanisms.

  4. 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...

  5. Synthesis of Cu, Zn and Cu/Zn brass alloy nanoparticles from metal amidinate precursors in ionic liquids or propylene carbonate with relevance to methanol synthesis

    OpenAIRE

    Schütte, K.; H. Meyer; Gemel, Chr.; Barthel, Juri; Fischer, R.A.; Janiak,Chr.

    2014-01-01

    Microwave-induced decomposition of the transition metal amidinates {[Me(C(NiPr)2)]Cu}2 (1) and [Me(C(NiPr)2)]2Zn (2) in the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm][BF4]) or in propylene carbonate (PC) gives copper and zinc nanoparticles which are stable in the absence of capping ligands (surfactants) for more than six weeks. Co-decomposition of 1 and 2 yields the intermetallic nano-brass phases β-CuZn and γ-Cu3Zn depending on the chosen molar ratios of the precursor...

  6. Preparation of Dispersed Platinum Nanoparticles on a Carbon Nanostructured Surface Using Supercritical Fluid Chemical Deposition

    Directory of Open Access Journals (Sweden)

    Mineo Hiramatsu

    2010-03-01

    Full Text Available We have developed a method of forming platinum (Pt nanoparticles using a metal organic chemical fluid deposition (MOCFD process employing a supercritical fluid (SCF, and have demonstrated the synthesis of dispersed Pt nanoparticles on the surfaces of carbon nanowalls (CNWs, two-dimensional carbon nanostructures, and carbon nanotubes (CNTs. By using SCF-MOCFD with supercritical carbon dioxide as a solvent of metal-organic compounds, highly dispersed Pt nanoparticles of 2 nm diameter were deposited on the entire surface of CNWs and CNTs. The SCF-MOCFD process proved to be effective for the synthesis of Pt nanoparticles on the entire surface of intricate carbon nanostructures with narrow interspaces.

  7. Simulation of the Kinetics of Growth of Iron Nanoparticles in the Process of Chemical Vapor Deposition of Hydrocarbons with Injection of Ferrocene for the Synthesis of Carbon-Nanotube Arrays

    Science.gov (United States)

    Futko, S. I.; Shulitskii, B. G.; Labunov, V. A.; Ermolaeva, E. M.

    2015-11-01

    A kinetic model of growth of iron nanoparticles in the process of synthesis of carbon-nanotube arrays in an injection-type reactor of chemical vapor deposition, in which iron nanoparticles are formed as a result of the coalescence of iron atoms representing products of the thermal decomposition of a mixture of ferrocene with xylene, has been developed. It is shown that the formation of iron nanoparticles in the indicated reactor is very nonequilibrium in character. The parametric dependences of the monodisperse distributions of iron nanoparticles by their diameter, number density, and volume fraction on the flow rate of nitrogen, the temperature of the high-temperature region in the reactor, and the concentration of ferrocene in xylene have been obtained. The calculations performed have shown that the diameter of the iron nanoparticles formed increases monotonically with increase in the temperature of the chemical vapor deposition of hydrocarbons and the concentration of ferrocene in xylene and, quite the reverse, decreases monotonically with increase in the rate of the nitrogen flow. The calculated and experimental diameters of the iron nanoparticles formed at mass fractions of ferrocene in xylene of 0.5-10% were compared. The model proposed can be used for calculating the synthesis of carbon nanotubes in a chemical-vapor-deposition reactor of the injection type.

  8. 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.

  9. Enzymatic synthesis of magnetic nanoparticles.

    Science.gov (United States)

    Kolhatkar, Arati G; Dannongoda, Chamath; Kourentzi, Katerina; Jamison, Andrew C; Nekrashevich, Ivan; Kar, Archana; Cacao, Eliedonna; Strych, Ulrich; Rusakova, Irene; Martirosyan, Karen S; Litvinov, Dmitri; Lee, T Randall; Willson, Richard C

    2015-01-01

    We report the first in vitro enzymatic synthesis of paramagnetic and antiferromagnetic nanoparticles toward magnetic ELISA reporting. With our procedure, alkaline phosphatase catalyzes the dephosphorylation of l-ascorbic-2-phosphate, which then serves as a reducing agent for salts of iron, gadolinium, and holmium, forming magnetic precipitates of Fe45±14Gd5±2O50±15 and Fe42±4Ho6±4O52±5. The nanoparticles were found to be paramagnetic at 300 K and antiferromagnetic under 25 K. Although weakly magnetic at 300 K, the room-temperature magnetization of the nanoparticles found here is considerably greater than that of analogous chemically-synthesized LnxFeyOz (Ln = Gd, Ho) samples reported previously. At 5 K, the nanoparticles showed a significantly higher saturation magnetization of 45 and 30 emu/g for Fe45±14Gd5±2O50±15 and Fe42±4Ho6±4O52±5, respectively. Our approach of enzymatically synthesizing magnetic labels reduces the cost and avoids diffusional mass-transfer limitations associated with pre-synthesized magnetic reporter particles, while retaining the advantages of magnetic sensing. PMID:25854425

  10. Enzymatic Synthesis of Magnetic Nanoparticles

    Directory of Open Access Journals (Sweden)

    Arati G. Kolhatkar

    2015-04-01

    Full Text Available We report the first in vitro enzymatic synthesis of paramagnetic and antiferromagnetic nanoparticles toward magnetic ELISA reporting. With our procedure, alkaline phosphatase catalyzes the dephosphorylation of l-ascorbic-2-phosphate, which then serves as a reducing agent for salts of iron, gadolinium, and holmium, forming magnetic precipitates of Fe45±14Gd5±2O50±15 and Fe42±4Ho6±4O52±5. The nanoparticles were found to be paramagnetic at 300 K and antiferromagnetic under 25 K. Although weakly magnetic at 300 K, the room-temperature magnetization of the nanoparticles found here is considerably greater than that of analogous chemically-synthesized LnxFeyOz (Ln = Gd, Ho samples reported previously. At 5 K, the nanoparticles showed a significantly higher saturation magnetization of 45 and 30 emu/g for Fe45±14Gd5±2O50±15 and Fe42±4Ho6±4O52±5, respectively. Our approach of enzymatically synthesizing magnetic labels reduces the cost and avoids diffusional mass-transfer limitations associated with pre-synthesized magnetic reporter particles, while retaining the advantages of magnetic sensing.

  11. 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...

  12. Radiation Synthesis of Nanoparticles

    International Nuclear Information System (INIS)

    Radiation processing of nano materials is one of the many applications of ionising radiation. It has the advantages of cold process, fast, homogeneous and clean processing without using chemicals, heat and no release of any volatile organic compounds. Hence, radiation processing can be categorised as a green process. The applications of ionising radiation for materials processing are well established and commercialized by way of crosslinking, grafting, curing and degradation. However, the materials use, condition of processing and the end products varies and radiation processing is continue to be developed for various applications in industry, agriculture, health care and environment. The new and emerging development of nano materials has also being incorporated in radiation processing whereby we can see the convergence of radiation and nano technology, to take advantages of the inherent properties of nano size particles. Nowadays many works are being carried out on radiation processing of nano materials. The incorporation of such nanoparticles in polymeric materials will render specific properties that find several advantages compare to conventional composites such as increase heat resistant, improve abrasion and scratch resistant and enhance mechanical properties. In recent years, polymer/clay nano composites has attracted the interest of industry because of its major improvements in physical and mechanical properties, heat stability, reduce flammability and provide enhanced barrier properties at low clay contents. In many applications, crosslinking of polymer matrix is necessary that can further improved the mechanical and physical properties of the composites. Similar research has been extended to electron beam crosslinking of electromagnetic nano composites which comprise of high volume fraction of inorganic fillers in elastomeric matrix. The effect of radiation on inorganic fillers is believed to has influence on the overall radiation crosslinking of the

  13. Multiwalled Carbon Nanotubes Decorated with Cobalt Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    D. G. Larrude

    2012-01-01

    Full Text Available Multiwalled carbon nanotubes (MWCNTs synthesized by spray pyrolysis were decorated with cobalt oxide nanoparticles using a simple synthesis route. This wet chemistry method yielded nanoparticles randomly anchored to the surface of the nanotubes by decomposition of cobalt nitrate hexahydrate diluted in acetone. Electron microscopy analysis indicated that dispersed particles were formed on the MWCNTs walls. The average size increased with the increasing concentration of cobalt nitrate in acetone in the precursor mixture. TEM images indicated that nanoparticles were strongly attached to the tube walls. The Raman spectroscopy results suggested that the MWCNT structure was slightly damaged after the nanoparticle growth.

  14. A Green and Facile Synthesis of Carbon-Incorporated Co3O4 Nanoparticles and Their Photocatalytic Activity for Hydrogen Evolution

    OpenAIRE

    Libo Gao; Jiangtao Diwu; Qiang Zhang; Hongyan Xu; Xiujian Chou; Jun Tang; Chenyang Xue

    2015-01-01

    Carbon-incorporated Co3O4 nanoparticles with an average diameter of 50 nm were prepared via a facile and environmentally friendly one-pot carbon-assisted method using degreasing cotton as a template as well as a reactant. The elemental analysis indicates the incorporation of carbon species into the Co3O4 nanoparticles and the XPS measurements demonstrate the presence of carbon species which comes from the incomplete combustion of the degreasing cotton. Interestingly, the resultant sample was ...

  15. 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...

  16. 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.

  17. Facile synthesis of β-lactoglobulin-functionalized multi-wall carbon nanotubes and gold nanoparticles on glassy carbon electrode for electrochemical sensing.

    Science.gov (United States)

    Du, Xin; Miao, Zhiying; Zhang, Di; Fang, Yuxin; Ma, Min; Chen, Qiang

    2014-12-15

    A facile approach was developed for the preparation of nanocomposite based on β-lactoglobulin (BLG)-functionalized multi-wall carbon nanotubes (MWCNTs) and gold nanoparticles (GNPs) for the first time. Owing to the amphipathic nature, BLG can be adopted onto the surface of MWCNTs to form BLG-MWCNTs with uniform dispersion in water. Taking advantage of sulfhydryl groups on BLG-MWCNTs, GNPs were decorated on the BLG-MWCNTs-modified glassy carbon electrode (GCE) by electrodeposition. The nanocomposite was characterized by transmission electron microscopy, scanning electron microscopy and X-ray spectroscopy analysis. Cyclic voltammetry and chronoamperometric method were used to evaluate the electrocatalytic ability of the nanocomposite. Furthermore, a glucose biosensor was developed based on the immobilization of glucose oxidase with cross-linking in the matrix of bovine serum albumin (BSA) on the nanocomposite modified GCE. The resulting biosensor exhibited high sensitivity (3.98 μA mM(-1)), wider linear range (0.025-5.5 mM), low detection limit (1.1 μM at the signal-to-noise ratio of 3) and fast response time (within 7s) for glucose detection. PMID:24984286

  18. A Novel Technique of Synthesis of Highly Fluorescent Carbon Nanoparticles from Broth Constituent and In-vivo Bioimaging of C. elegans.

    Science.gov (United States)

    Pramanik, A; Kole, A K; Krishnaraj, R N; Biswas, S; Tiwary, C S; Varalakshmi, P; Rai, S K; Kumar, B A; Kumbhakar, P

    2016-09-01

    Here we have demonstrated a novel single step technique of synthesis of highly fluorescent carbon nanoparticles (CNPs) from broth constituent and in vivo bioimaging of Caenorhabditis elegans (C. elegans) with the synthesized CNPs has been presented. The synthesized CNPs has been characterized by the UV-visible (UV-Vis) absorption spectroscopy, transmission electron microscopy (TEM) and Raman studies. The sp (2) cluster size of the synthesized samples has been determined from the measured Raman spectra by fitting it with the theoretical skew Lorentzian (Breit-Wigner- Fano (BWF)) line shape. The synthesised materials are showing excitation wavelength dependent tunable photoluminescence (PL) emission characteristics with a high quantum yield (QY) of 3 % at a very low concentration of CNPs. A remarkable increase in the intensity of PL emission from 16 % to 39 % in C. elegans has also been observed when the feeding concentration of CNPs to C. elegans is increased from 0.025 % to 0.1 % (w/v). The non-toxicity and water solubility of the synthesized material makes it ideal candidate for bioimaging. PMID:27380200

  19. 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.

  20. 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

  1. 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.

  2. New Synthesis of Pt-Ru Nanoparticles on Surface Modified Carbon Vulcane XC-72 as an Effective Catalyst for Direct Methanol Fuel Cell

    Institute of Scientific and Technical Information of China (English)

    Ahmad; Nozad; Golikand; Sajjad; Sadaghat; Sharehjini; Mohammad; Yari

    2007-01-01

    1 Results Pt-Ru nanoparticles are synthesised on the surface oxidized carbon Vulcane XC-72 as catalyst support by chemically anchoring Pt and Ru onto the surface of modified carbon vulcane XC-72 (by refluxing in 70% HNO3 at 120 ℃ for 12 h to introduce surface functional groups) .The nanoparticles of Pt and Ru are synthesized by reduction of H2PtCl6 and K4Ru(CN)6 with sodium borohydride in a 5.5 buffer solution of sodium citrate,the complexation of citrate with metal ions is beneficial to the formati...

  3. A Green and Facile Synthesis of Carbon-Incorporated Co3O4 Nanoparticles and Their Photocatalytic Activity for Hydrogen Evolution

    Directory of Open Access Journals (Sweden)

    Libo Gao

    2015-01-01

    Full Text Available Carbon-incorporated Co3O4 nanoparticles with an average diameter of 50 nm were prepared via a facile and environmentally friendly one-pot carbon-assisted method using degreasing cotton as a template as well as a reactant. The elemental analysis indicates the incorporation of carbon species into the Co3O4 nanoparticles and the XPS measurements demonstrate the presence of carbon species which comes from the incomplete combustion of the degreasing cotton. Interestingly, the resultant sample was able to split pure water into hydrogen under visible light irradiation without any cocatalyst, which is mainly due to the enhanced light absorption behavior confirmed by the UV-Vis absorption spectra. This facile method provided a potential strategy for applying narrow bandgap semiconductors in pure water splitting.

  4. Facile Synthesis of Au or Ag Nanoparticles-Embedded Hollow Carbon Microspheres from Metal-Organic Framework Hybrids and Their Efficient Catalytic Activities.

    Science.gov (United States)

    Choi, Sora; Lee, Hee Jung; Oh, Moonhyun

    2016-05-01

    Au or Ag nanoparticles-embedded hollow carbon spheres, which display outstanding catalytic activity and excellent recyclability, are prepared by a one-step pyrolysis of metal-organic framework (MOF) hybrids consisting of polystyrene cores and MOF shells loaded with noble metal ions (polystyrene@ZIF-8/M(n+) ; M(n+) = Au(3+) or Ag(+) ). PMID:27151828

  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. Size dependent phase diagrams of Nickel-Carbon nanoparticles

    CERN Document Server

    Magnin, Yann; Amara, Hakim; Ducastelle, François; Bichara, Christophe

    2015-01-01

    The carbon rich phase diagrams of nickel-carbon nanoparticles, relevant to catalysis and catalytic chemical vapor deposition synthesis of carbon nanotubes, are calculated for system sizes up to about 3 nanometers (807 Ni atoms). A tight binding model for interatomic interactions drives the Grand Canonical Monte Carlo simulations used to locate solid, core/shell and liquid stability domains, as a function of size, temperature and carbon chemical potential or concentration. Melting is favored by carbon incorporation from the nanoparticle surface, resulting in a strong relative lowering of the eutectic temperature and a phase diagram topology different from the bulk one. This should be taken into account in our understanding of the nanotube growth mechanisms.

  7. 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.

  8. Poly(acrylic acid)-regulated Synthesis of Rod-Like Calcium Carbonate Nanoparticles for Inducing the Osteogenic Differentiation of MC3T3-E1 Cells.

    Science.gov (United States)

    Yang, Wei; Yao, Chenxue; Cui, Zhengyang; Luo, Dandan; Lee, In-Seop; Yao, Juming; Chen, Cen; Kong, Xiangdong

    2016-01-01

    Calcium carbonate, especially with nanostructure, has been considered as a good candidate material for bone regeneration due to its excellent biodegradability and osteoconductivity. In this study, rod-like calcium carbonate nanoparticles (Rod-CC NPs) with desired water dispersibility were achieved with the regulation of poly (acrylic acid). Characterization results revealed that the Rod-CC NPs had an average length of 240 nm, a width of 90 nm with an average aspect ratio of 2.60 and a negative ζ-potential of -22.25 ± 0.35 mV. The degradation study illustrated the nanoparticles degraded 23% at pH 7.4 and 45% at pH 5.6 in phosphate-buffered saline (PBS) solution within three months. When cultured with MC3T3-E1 cells, the Rod-CC NPs exhibited a positive effect on the proliferation of osteoblast cells. Alkaline phosphatase (ALP) activity assays together with the osteocalcin (OCN) and bone sialoprotein (BSP) expression observations demonstrated the nanoparticles could induce the differentiation of MC3T3-E1 cells. Our study developed well-dispersed rod-like calcium carbonate nanoparticles which have great potential to be used in bone regeneration. PMID:27164090

  9. Poly(acrylic acid-regulated Synthesis of Rod-Like Calcium Carbonate Nanoparticles for Inducing the Osteogenic Differentiation of MC3T3-E1 Cells

    Directory of Open Access Journals (Sweden)

    Wei Yang

    2016-05-01

    Full Text Available Calcium carbonate, especially with nanostructure, has been considered as a good candidate material for bone regeneration due to its excellent biodegradability and osteoconductivity. In this study, rod-like calcium carbonate nanoparticles (Rod-CC NPs with desired water dispersibility were achieved with the regulation of poly (acrylic acid. Characterization results revealed that the Rod-CC NPs had an average length of 240 nm, a width of 90 nm with an average aspect ratio of 2.60 and a negative ζ-potential of −22.25 ± 0.35 mV. The degradation study illustrated the nanoparticles degraded 23% at pH 7.4 and 45% at pH 5.6 in phosphate-buffered saline (PBS solution within three months. When cultured with MC3T3-E1 cells, the Rod-CC NPs exhibited a positive effect on the proliferation of osteoblast cells. Alkaline phosphatase (ALP activity assays together with the osteocalcin (OCN and bone sialoprotein (BSP expression observations demonstrated the nanoparticles could induce the differentiation of MC3T3-E1 cells. Our study developed well-dispersed rod-like calcium carbonate nanoparticles which have great potential to be used in bone regeneration.

  10. Synthesis of All-carbon Chains and Nanoparticles by Chemical Transformation of Halogenated Hydrocarbons at Low Temperatures

    Czech Academy of Sciences Publication Activity Database

    Kavan, Ladislav

    č. 196 (2001), s. 22-38. ISSN 0371-5345 R&D Projects: GA ČR GA203/98/1168; GA ČR GA203/99/1015; GA ČR GA203/00/0634 Institutional research plan: CEZ:AV0Z4040901 Keywords : halogenated hydrocarbon * electrochemical carbon * fullerenes Subject RIV: CG - Electrochemistry

  11. 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...

  12. Synthesis of Carbon Nanotubes by MWPCVD at Low Temperature

    Institute of Scientific and Technical Information of China (English)

    王升高; 汪建华; 王传新; 马志彬; 满卫东

    2002-01-01

    Growth of carbon nanotubes (CNTs) at low temperature is very important to the applications of nanotubes. In this paper, under the catalytic effect of cobalt nanoparticles supported by SiO2, CNTs were synthesized by microwave plasma chemical vapor deposition (MWPCVD)below 500℃. It demonstrates that MWPCVD can be a very efficient process for the synthesis of CNTs at low temperature.

  13. Hydrothermal Synthesis of Platinum Group Metal Nanoparticles

    OpenAIRE

    Krehula, Stjepko; Musić, Svetozar

    2011-01-01

    A novel route for the synthesis of platinum group metal nanoparticles has been reported. The synthesis is based on the addition of tetramethylammonium hydroxide (TMAH) to the aqueous PtCl4, IrCl3 or Rh(NO3)3 solution followed by the hydrothermal treatment of these precipitation systems at 160 ºC. The mean size of nanoparticles was 9.2 nm for platinum, 21 nm for iridium, and 28 nm for rhodium. The average crystallite size was estimated at 7.4 nm for platinum, 3.1 nm for iridium and...

  14. Synthesis and characterization of carbon or/and boron-doped CdS nanoparticles and investigation of optical and photoluminescence properties

    International Nuclear Information System (INIS)

    Un-doped and carbon or/and boron doped Cadmium sulfide nanoparticles were prepared via chemical co-precipitation procedure by Polyvinyl pyrrolidone (PVP) as a stabilizer. The optical and structural properties were investigated using several techniques. The morphology of CdS nanophotocatalyst was characterized using X-ray diffraction (XRD) and scanning electron microscopy. The optical properties of both un-doped and doped samples were carried out by photoluminescence (PL) spectroscopy and UV–vis Diffuse reflectance spectra (DRS). An optimum doping level of the atoms dopant for enhanced PL properties are found through optical study. Degradation of Amoxicillin under UV light elucidation was applied to appraise the photocatalytic efficiency. The results show that the carbon and boron doping CdS nanoparticles has high potential in green chemistry. - Highlights: • Un-doped, C or/and B-doped CdS nanoparticles were successfully synthesized. • The Blue shift was observed in UV–vis absorption spectra for the doped nanoparticles. • Doping of CdS with C and B enhances the fluorescence

  15. Synthesis and characterization of carbon or/and boron-doped CdS nanoparticles and investigation of optical and photoluminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Fakhri, Ali, E-mail: ali.fakhri88@yahoo.com [Department of Chemistry, Shahr-e-Qods Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Young Researchers and Elite Club, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Khakpour, Reza [Department of Physics, Tehran North Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of)

    2015-04-15

    Un-doped and carbon or/and boron doped Cadmium sulfide nanoparticles were prepared via chemical co-precipitation procedure by Polyvinyl pyrrolidone (PVP) as a stabilizer. The optical and structural properties were investigated using several techniques. The morphology of CdS nanophotocatalyst was characterized using X-ray diffraction (XRD) and scanning electron microscopy. The optical properties of both un-doped and doped samples were carried out by photoluminescence (PL) spectroscopy and UV–vis Diffuse reflectance spectra (DRS). An optimum doping level of the atoms dopant for enhanced PL properties are found through optical study. Degradation of Amoxicillin under UV light elucidation was applied to appraise the photocatalytic efficiency. The results show that the carbon and boron doping CdS nanoparticles has high potential in green chemistry. - Highlights: • Un-doped, C or/and B-doped CdS nanoparticles were successfully synthesized. • The Blue shift was observed in UV–vis absorption spectra for the doped nanoparticles. • Doping of CdS with C and B enhances the fluorescence.

  16. Synthesis and characterizations of CoPt nanoparticles supported on poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) functionalized multi-walled carbon nanotubes with superior activity for NaBH4 hydrolysis

    International Nuclear Information System (INIS)

    Highlights: • Simple strategy for the synthesis of CoPt-PEDOT:PSS/MWCNTs. • PEDOT:PSS as a modifier of MWCNTs can improve the particles dispersion. • Superior catalytic activities for the NaBH4 hydrolysis reaction. - Abstract: We present here a facile strategy for synthesis of CoPt nanoparticles supported on poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS) functionalized multi-walled carbon nanotubes (MWCNTs). The as-prepared CoPt-PEDOT:PSS/MWCNT catalyst was characterized with UV–vis spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction and X-ray photoelectron. The well-supported and low-Pt-content nanostructure catalyst exhibits superior catalytic activity for the NaBH4 hydrolysis reaction with a 47.3 kJ mol−1 of activation energy. The maximum hydrogen generation rate is 6900 mL min−1 g−1 at 298 K

  17. 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

  18. Synthesis, characterization and applications of magnetite nanoparticles

    Science.gov (United States)

    Kanmukhla, Vikram Kumar

    In the past few years, the synthesis of magnetic nanoparticles has received considerable attention due to their potential use in clinical applications. Since the properties of these nanoparticles depend strongly on their size, shape and crystallinity, there is a need for a general method to produce these particles with a controlled size, shape and crystal type. Of the many magnetic materials (Co, Ni, and Fe), the magnetite (Fe3O 4) is least toxic and hence most promising for applications in medical diagnostics. Microemulsion-based synthesis utilizes the local aqueous environment within a reverse micelle as a nano-scale reactor and allows synthesizing nanoparticles with a hydrophilic surface for subsequent functionalization. By controlling the water-to-surfactant ratio, the type of surfactants, and the ionic strength of the aqueous core, one can control the size and shape of the resulting particles. We developed such a system that allows the multi-step synthesis of surface-functionalized, magnetic nanoparticles in a one-pot synthesis reaction. By altering the system chemistry, we were further able to produce either spheres or cylinders of controlled dimension in the size range of 5 nm to 30 nm. Using standard bio-conjugation techniques, we successfully immobilized an enzyme onto the nanoparticles. We also developed a theoretical model for the separation and fractionation of nanoparticles based on their size and magnetic properties. Using the multiphysics and finite element modeling capabilities of FEMLAB(TM), we solved the coupled system of PDEs describing the interaction of magnetic particles within a magnetic field for either static (cylindrical beaker) or convective flow (capillary) conditions. A net retention time as high as 310 s is achieved for 200 nm particles at field strength of 1250 kA/m. The model allows the design of a magnetic, field-flow fractionation (MFFF) system to separate nanoparticles by size.

  19. A novel synthesis of perovskite bismuth ferrite nanoparticles

    Directory of Open Access Journals (Sweden)

    Alexandre Z. Simões

    2011-09-01

    Full Text Available Microwave assisted hydrothermal (MAH method was used to synthesize crystalline bismuth ferrite (BiFeO3 nanoparticles (BFO at temperature of 180°C with times ranging from 5 min to 1 h. For comparison, BFO powders were also crystallized by the soft chemistry route in a conventional furnace at a temperature of 850°C for 4 h. X-ray diffraction (XRD results verified the formation of perovskite BFO crystallites while infrared data showed no traces of carbonate. Field emission scanning microcopy (FE/SEM revealed a homogeneous size distribution of nanometric BFO powders. MAH method produced nanoparticles of 96% pure perovskite, with a size of 130 nm. These results are in agreement with Raman scattering values which show that the MAH synthesis route is rapid and cost effective. This method could be used as an alternative to other chemical methods in order to obtain BFO nanoparticles.

  20. 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.

  1. 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)

  2. 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.

  3. Synthesis of nickel oxides nanoparticles on glassy carbon as an electron transfer facilitator for horseradish peroxidase: Direct electron transfer and H2O2 determination

    International Nuclear Information System (INIS)

    In this study, horseradish peroxidase/nickel oxides nanoparticles/glassy carbon (HRP/NiO NPs/GC) electrode was prepared by first applying nickel oxides nanoparticles on glassy carbon surface and then horseradish peroxidase immobilized on the NiO NPs. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) have been used as a diagnostic tools to identify the synthesized NiO NPs. Immobilized HRP showed an electrochemical redox behavior pertained to HRP(Fe(III)-Fe(II)) by direct electron transfer between protein and nanoparticles with a formal potential (E0') of - 55.5 mV (vs. Ag/AgCl and 141.5 mV vs. NHE) in 50 mM phosphate buffer solution (PBS). The anodic charge transfer coefficient (α) and heterogeneous electron transfer rate constant (ks) were 0.42 and 0.75 s-1, respectively. Biocatalytic activity of HRP/NiO NPs/GC electrode for reduction of hydrogen peroxide and application to hydrogen peroxide determination was exemplified.

  4. Facile synthesis of silver nanoparticles supported on three dimensional graphene oxide/carbon black composite and its application for oxygen reduction reaction

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Ag nanoparticles were prepared using GO as reductant without any stabilizers. • A composite support with a 3D structure was constructed by GO and carbon black. • The Ag/GO/C composite shows enhanced ORR activity compared with Ag/GO. - Abstract: A 3D graphene oxide/carbon sphere supported silver composite (Ag/GO/C) was synthesized using graphene oxide as the reducing agent. The reducing process of Ag+ was monitored by the ultra violet-visible (UV-vis) absorption spectrometer and the physical properties of the Ag/GO/C composite were characterized by Fourier transform infrared spectrometer (FTIR), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The results demonstrated that the dispersive Ag nanoparticles are anchored uniformly on the surface of GO sheets with a mean size of about 6.9 nm. With introducing carbon black, the Ag nanoparticles aggregated slightly. Compared with its counterpart Ag/GO, the Ag/GO/C composite showed a significantly enhanced activity towards the oxygen reduction reaction in alkaline media. The enhancement can be ascribed to the 3D composite support, which not only improves the electrical conductivity, but also enforces the mass transport in the catalyst layer facilitating the reactants access to the active sites. Moreover, the Ag/GO/C composite exhibits good tolerance to alcohols, carbonates and tetramethylammonium hydroxide. This work is expected to open a new pathway to use GO as a reducing agent to synthesize electrocatalysts without surfactants

  5. Carbon doped ZnO: Synthesis, characterization and interpretation

    International Nuclear Information System (INIS)

    A novel thermal plasma in-flight technique has been adopted to synthesize nanocrystalline ZnO and carbon doped nanocrystalline ZnO matrix. Transmission electron microscopy (TEM) studies on these samples show the average particle sizes to be around 32 nm for ZnO and for carbon doped ZnO. An enhancement of saturation magnetization in nanosized carbon doped ZnO matrix by a factor of 3.8 has been found in comparison to ZnO nanoparticles at room temperature. Raman measurement clearly indicates the presence of Zn–C complexes surrounded by ZnO matrix in carbon doped ZnO. This indicates that the ferromagnetic signature in carbon doped ZnO arises from the creation of defects or the development of oxy-carbon clusters, in the carbon doped ZnO system. Theoretical studies based on density functional theory also support the experimental analyses. - Highlights: ► Synthesis of nanocrystalline ZnO and carbon doped ZnO matrix by inflight thermal plasma reactor. ► Enhancement of ferromagnetism in nanosized carbon doped ZnO in comparison to ZnO nanoparticles. ► Raman measurement indicates the presence of Zn–C complexes surrounded by ZnO matrix. ► Ferromagnetic signature in carbon doped ZnO arises from the development of oxy-carbon clusters. ► DFT supports experimental evidence of ferromagnetism in C doped ZnO nanoparticles.

  6. 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.

  7. A low-temperature synthesis of electrochemical active Pt nanoparticles and thin films by atomic layer deposition on Si(111) and glassy carbon surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Rui [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Han, Lihao [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Huang, Zhuangqun; Ferrer, Ivonne M. [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Smets, Arno H.M.; Zeman, Miro [Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Brunschwig, Bruce S., E-mail: bsb@caltech.edu [Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Lewis, Nathan S., E-mail: nslewis@caltech.edu [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Kavli Nanoscience Institute, California Institute of Technology, Pasadena, CA 91125 (United States)

    2015-07-01

    Atomic layer deposition (ALD) was used to deposit nanoparticles and thin films of Pt onto etched p-type Si(111) wafers and glassy carbon discs. Using precursors of MeCpPtMe{sub 3} and ozone and a temperature window of 200–300 °C, the growth rate was 80–110 pm/cycle. X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM) were used to analyze the composition, structure, morphology, and thickness of the ALD-grown Pt nanoparticle films. The catalytic activity of the ALD-grown Pt for the hydrogen evolution reaction was shown to be equivalent to that of e-beam evaporated Pt on glassy carbon electrode. - Highlights: • Pure Pt films were grown by atomic layer deposition (ALD) using MeCpPtMe3 and ozone. • ALD-grown Pt thin films had high growth rates of 110 pm/cycle. • ALD-grown Pt films were electrocatalytic for hydrogen evolution from water. • Electrocatalytic activity of the ALD Pt films was equivalent to e-beam deposited Pt. • No carbon species were detected in the ALD-grown Pt films.

  8. A low-temperature synthesis of electrochemical active Pt nanoparticles and thin films by atomic layer deposition on Si(111) and glassy carbon surfaces

    International Nuclear Information System (INIS)

    Atomic layer deposition (ALD) was used to deposit nanoparticles and thin films of Pt onto etched p-type Si(111) wafers and glassy carbon discs. Using precursors of MeCpPtMe3 and ozone and a temperature window of 200–300 °C, the growth rate was 80–110 pm/cycle. X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM) were used to analyze the composition, structure, morphology, and thickness of the ALD-grown Pt nanoparticle films. The catalytic activity of the ALD-grown Pt for the hydrogen evolution reaction was shown to be equivalent to that of e-beam evaporated Pt on glassy carbon electrode. - Highlights: • Pure Pt films were grown by atomic layer deposition (ALD) using MeCpPtMe3 and ozone. • ALD-grown Pt thin films had high growth rates of 110 pm/cycle. • ALD-grown Pt films were electrocatalytic for hydrogen evolution from water. • Electrocatalytic activity of the ALD Pt films was equivalent to e-beam deposited Pt. • No carbon species were detected in the ALD-grown Pt films

  9. Carbon nanotubes: synthesis and functionalization

    OpenAIRE

    Andrews, Robert

    2007-01-01

    This thesis focuses on two of the major challenges of carbon nanotube (CNT) research: understanding the growth mechanism of nanotubes by chemical vapour deposition (CVD) and the positioning of nanotubes on surfaces. The mechanism of growth of single–walled nanotubes (SWNTs) has been studied in two ways. Firstly, a novel iron nanoparticle catalyst for the production of single–walled nanotubes was developed. CVD conditions were established that produced high quality tubes. These optimised C...

  10. Copper nanoparticle modified carbon electrode for determination of dopamine

    International Nuclear Information System (INIS)

    This paper reports the synthesis and characterization of copper nanoparticles (CuNPs) and application of copper nanoparticle-modified glassy carbon electrode for the electrochemical determination of dopamine. Electrochemical measurements were performed using differently modified glassy carbon (GC) electrodes. Bare, oxidized before modification and copper nanoparticle-modified glassy carbon electrodes (bare-GC, ox-GC and CuNP/GC electrodes, respectively) were characterized by cyclic voltammetry and electrochemical impedance spectroscopy in the presence of redox probes. Atomic force microscopy was used for the visualization of electrode surfaces. The CuNP/GC electrode was found to be suitable for the selective determination of dopamine even in the presence of ascorbic acid, uric acid, and p-acetamidophenol. The observed linear range of CuNP/GC for dopamine was from 0.1 nM to 1.0 μM while the detection limit was estimated to be 50 pM. It was demonstrated that here reported glassy carbon electrode modified by copper nanoparticles is suitable for the determination of dopamine in real samples such as human blood serum.

  11. 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.

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

    OpenAIRE

    Thomas Hanemann; Dorothée Vinga Szabó

    2010-01-01

    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 thermomechani...

  13. Facile synthesis of palladium nanoparticles supported on multi-walled carbon nanotube for efficient hydrogenation of biomass-derived levulinic acid

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Kai, E-mail: kyan@lakeheadu.ca; Lafleur, Todd [Lakehead University, Department of Chemistry (Canada); Liao, Jiayou [Tianjin University, School of Chemical Engineering and Technology (China)

    2013-09-15

    Different loading of palladium (Pd) nanoparticles were successfully fabricated on multi-walled carbon nanotubes using Pd acetylacetonate as the precursor via a simple liquid impregnation method. The crystal phase, morphology, textural structure and the chemical state of the resulting Pd nanoparticles (Pd/CNT) catalysts were studied and the characterization results indicated that the uniform dispersion of small Pd nanoparticles with the size range of 1.0-4.5 nm was achieved. The synthesized Pd/CNT catalysts exhibited efficient performance for the catalytic hydrogenation of biomass-derived levulinic acid into biofuel {gamma}-valerolactone. In comparison with the commercial 5 wt% Pd/C and the 5 wt% Pd/CNT catalyst prepared by Pd nitrate precursor, much higher activities were achieved, whereas the biofuel {gamma}-valerolactone was highly produced with 56.3 % yield at 57.6 % conversion of levulinic acid on the 5 wt% Pd/CNT catalyst under mild conditions. The catalyst developed in this work may be a good candidate for the wide applications in the hydrogenation.

  14. Facile synthesis of palladium nanoparticles supported on multi-walled carbon nanotube for efficient hydrogenation of biomass-derived levulinic acid

    International Nuclear Information System (INIS)

    Different loading of palladium (Pd) nanoparticles were successfully fabricated on multi-walled carbon nanotubes using Pd acetylacetonate as the precursor via a simple liquid impregnation method. The crystal phase, morphology, textural structure and the chemical state of the resulting Pd nanoparticles (Pd/CNT) catalysts were studied and the characterization results indicated that the uniform dispersion of small Pd nanoparticles with the size range of 1.0–4.5 nm was achieved. The synthesized Pd/CNT catalysts exhibited efficient performance for the catalytic hydrogenation of biomass-derived levulinic acid into biofuel γ-valerolactone. In comparison with the commercial 5 wt% Pd/C and the 5 wt% Pd/CNT catalyst prepared by Pd nitrate precursor, much higher activities were achieved, whereas the biofuel γ-valerolactone was highly produced with 56.3 % yield at 57.6 % conversion of levulinic acid on the 5 wt% Pd/CNT catalyst under mild conditions. The catalyst developed in this work may be a good candidate for the wide applications in the hydrogenation

  15. Synthesis, characterization and magnetic properties of carbon nanotubes decorated with magnetic M{sup II}Fe{sub 2}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ali, Syed Danish [National Centre for Physics, Quaid-e-Azam University Campus, Islamabad (Pakistan); Department of Chemistry, University of Engineering and Technology, Lahore (Pakistan); Hussain, Syed Tajammul, E-mail: dr_tajammul@yahoo.ca [National Centre for Physics, Quaid-e-Azam University Campus, Islamabad (Pakistan); Gilani, Syeda Rubina [Department of Chemistry, University of Engineering and Technology, Lahore (Pakistan)

    2013-04-15

    In this study, a simple, efficient and reproducible microemulsion method was applied for the successful decoration of carbon nanotubes (CNTs) with magnetic M{sup II}Fe{sub 2}O{sub 4} (M = Co, Ni, Cu, Zn) nanoparticles. The structure, composition and morphology of the prepared nanocomposite materials were characterized using X-ray diffraction (XRD), Rutherford backscattering spectroscopy (RBS), Fourier transform infrared spectroscopy (FTIR) and Scanning electron microscopy (SEM). The magnetic properties were investigated by the vibrating sample magnetometer (VSM). The SEM results illustrated that large quantity of M{sup II}Fe{sub 2}O{sub 4} nanoparticles were uniformly decorated around the circumference of CNTs and the sizes of the nanoparticles ranged from 15 to 20 nm. Magnetic hysteresis loop measurements revealed that all the M{sup II}Fe{sub 2}O{sub 4}/CNTs nanocomposites displayed ferromagnetic behavior at 300 K and can be manipulated using an external magnetic field. The CoFe{sub 2}O{sub 4}/CNTs nanocomposite showed maximum value of saturation magnetization which was 37.47 emu g{sup −1}. The as prepared M{sup II}Fe{sub 2}O{sub 4}/CNTs nanocomposites have many potential application in magnetically guided targeted drug delivery, clinical diagnosis, electrochemical biosensing, magnetic data storage and magnetic resonance imaging.

  16. Effect of reduction enhancer on a radiolytic synthesis of carbon-supported Pt–Cu nanoparticles and their structural and electrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Kugai, Junichiro, E-mail: jkugai@kobe-kosen.ac.jp [Kobe City College of Technology, Department of Applied Chemistry (Japan); Kubota, Chihiro; Okazaki, Tomohisa; Seino, Satoshi; Nakagawa, Takashi [Osaka University, Graduate School of Engineering (Japan); Nitani, Hiroaki [High Energy Accelerator Research Organization, Institute of Materials Structure Science (IMSS) (Japan); Yamamoto, Takao A. [Osaka University, Graduate School of Engineering (Japan)

    2015-06-15

    In order to clarify the effect of reduction enhancer on the nanoparticle formation process and their structural and catalytic properties, carbon-supported Pt–Cu nanoparticles were synthesized by electron beam irradiation on an aqueous precursor solution in the presence/absence of reduction enhancer. In the absence of reduction enhancer, tetravalent platinum oxide particles of approximately 1 nm in diameter were formed on carbon support with copper barely precipitated, while in the presence of 2-propanol or ethylene glycol or glucose both platinum and copper precipitated as few-nanometer-sized alloy particles together with copper oxides. It was suggested that the metal nuclei produced upon electron beam irradiation do not have enough lifetime without reduction enhancer due to fast oxidation of the nuclei by oxidizing radicals, while the reduction enhancer scavenges these oxidizing radicals preventing oxidation of metallic clusters and prolonging their lifetime. Ethylene glycol gave smaller and better alloyed particles with less copper oxides compared to 2-propanol since the carbonyl compounds derived from oxidation of ethylene glycol protect metallic clusters from oxidation further prolonging their lifetime. In the electrochemical measurements, the methanol oxidation activities of Pt–Cu/C catalysts were well explained by their structural characteristics.

  17. Effect of reduction enhancer on a radiolytic synthesis of carbon-supported Pt–Cu nanoparticles and their structural and electrochemical properties

    International Nuclear Information System (INIS)

    In order to clarify the effect of reduction enhancer on the nanoparticle formation process and their structural and catalytic properties, carbon-supported Pt–Cu nanoparticles were synthesized by electron beam irradiation on an aqueous precursor solution in the presence/absence of reduction enhancer. In the absence of reduction enhancer, tetravalent platinum oxide particles of approximately 1 nm in diameter were formed on carbon support with copper barely precipitated, while in the presence of 2-propanol or ethylene glycol or glucose both platinum and copper precipitated as few-nanometer-sized alloy particles together with copper oxides. It was suggested that the metal nuclei produced upon electron beam irradiation do not have enough lifetime without reduction enhancer due to fast oxidation of the nuclei by oxidizing radicals, while the reduction enhancer scavenges these oxidizing radicals preventing oxidation of metallic clusters and prolonging their lifetime. Ethylene glycol gave smaller and better alloyed particles with less copper oxides compared to 2-propanol since the carbonyl compounds derived from oxidation of ethylene glycol protect metallic clusters from oxidation further prolonging their lifetime. In the electrochemical measurements, the methanol oxidation activities of Pt–Cu/C catalysts were well explained by their structural characteristics

  18. One-step solvothermal synthesis of Sn nanoparticles dispersed in ternary manganese-nickel-cobalt carbonate as superior anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Sn with high theoretical specific capacity has suffered from poor cycling stability due to its huge volume changes during charging/discharging processes. In this work, a novel structure of tin nanoparticles well dispersed in ternary manganese-nickel-cobalt carbonate Mn0.54 Ni0.13 Co0.13 (CO3)0.8 (MNCCO3) is synthesized using a facile one-step solvothermal process and demonstrates significantly improved electrochemical performance compared to Sn nanoparticles or bare MNCCO3. Additionally, Sn content can be optimized to maximize the battery performance of the composite. When tested as an anode material in lithium ion batteries, the composite with 10 wt.% Sn nanoparticles dispersed in MNCCO3 matrix (10Sn@MNCCO3) demonstrates the best performance, delivering a high initial charge capacity of 929 mAh/g and retains a specific capacity of 657 mAh/g after 50 cycles and 560 mAh/g after 100 cycles at a specific current of 100 mA/g. The charge capacity of 10Sn@MNCCO3 decreases from a value of 991 mAh/g when cycled at 50 mA/g to 64 mAh/g at 2000 mA/g with the increasing specific current. When the specific current returns from 2000 mA/g to 50 mA/g, 10Sn@MNCCO3 retains a high capacity of 791 mAh/g. The improved electrochemical performance can be ascribed to the synergic effect of both components in the composite, in which ternary carbonate MNCCO3 matrix not only provides high practical capacity, but also effectively accommodates the strain of dramatic volume change during long cycling, meanwhile Sn ensures a good electrical contact of the overall electrode due to its high electronic conductivity

  19. 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...

  20. 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...

  1. Sol–gel synthesis of Fe–Co nanoparticles and magnetization study

    International Nuclear Information System (INIS)

    We report the synthesis of carbon encapsulated Fe–Co nanoparticles using conventional sol–gel route and its magnetization studies. The x-ray diffraction indicates the formation of the single phase body centered cubic alloy Fe–Co phase with cell parameter of 2.857 Å. Nanoparticles are highly crystalline and exhibit low index faceting as determined from high-resolution transmission electron microscopy (HRTEM) investigation. The observed orthogonal lattice planes with lattice distance of 2.86 Å are attributed to (100) and (010). HRTEM image confirms the cube like Fe–Co nanoparticles with core–shell structure of carbon encapsulation, composed of carbon and graphite materials. The magnetometry results of the carbon encapsulated alloy Fe–Co nanoparticles with core–shell structure designate as a ferromagnetically ordered soft magnet with coercive field of 890 Oe (at 5 K). The coercive field and magnetization value depend on the size of nanoparticles as well as the diamagnetic contribution of carbon encapsulation. - Highlights: • Synthesis of highly pure alloy nanoparticles at ambient pressure and low temperature. • Carbon coating have been determined by electron microscope to explain their higher stability at room temperature and atmospheric conditions. • Magnetic interactions between Fe and Co ions have been proposed to explain the soft ferromagnetism

  2. Nanoparticle Synthesis from Cobalt Acetylacetonate

    Czech Academy of Sciences Publication Activity Database

    Moravec, Pavel; Smolík, Jiří; Levdansky, V.V.; Bakardjieva, Snejana

    Helsinki : -, 2010, P2J35. ISBN N. [International Aerosol Conference IAC 2010. Helsinki (FI), 29.08.2010-03.09.2010] R&D Projects: GA ČR GA104/07/1093 Institutional research plan: CEZ:AV0Z40720504; CEZ:AV0Z40320502 Keywords : hot wall reactor * nanoparticle generation * mocvd Subject RIV: CF - Physical ; Theoretical Chemistry www.iac2010.fi

  3. 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), ...

  4. An electrochemical sensor prepared by sonochemical one-pot synthesis of multi-walled carbon nanotube-supported cobalt nanoparticles for the simultaneous determination of paracetamol and dopamine

    International Nuclear Information System (INIS)

    Highlights: • A GCE was modified with carbon nanotubes and cobalt nanoparticles. • The composite material was obtained using an ultrasonic chemical deposition method. • The CoNPs/MWCNT/GCE was applied for the simultaneous determination of PAR and DA. • The presence of AA and UA did not affect the responses of PAR and DA. • Lower detection limits were obtained using the CoNPs/MWCNT/GCE. - Abstract: Multi-walled carbon nanotubes (MWCNTs) functionalized by cobalt nanoparticles were obtained using a single step chemical deposition method in an ultrasonic bath. The composite material was characterized using scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDX). The electroactivity of the cobalt-functionalized MWCNTs was assessed in respect to the electrooxidation of paracetamol (PAR) and dopamine (DA). It was found that the carbon nanotube supported cobalt nanoparticles have significantly higher catalytic properties. The proposed electrode has been applied for the simultaneous determination of PAR and DA. The modified electrode could resolve the overlapped voltammetric waves of PAR and DA into two well-defined voltammetric peaks with peak to peak separation of about 203 mV. On the other hand, the presence of potential drug interfering compounds AA and UA did not affect the voltammetric responses of PAR and DA. The current of oxidation peaks showed a linear dependent on the concentrations of PAR and DA in the range of 5.2 × 10−9–4.5 × 10−7 M (R2 = 0.9987) and 5.0 × 10−8–3.0 × 10−6 M (R2 = 0.9999), respectively. The detection limits of 1.0 × 10−9 M and 1.5 × 10−8 M were obtained for PAR and DA, respectively. The proposed electrode showed good stability (peak current change: 4.9% with and RSD of 2.6% for PAR; 5.5% with and RSD of 3.0% for DA over 3 weeks), reproducibility (RSD 2.3% for PAR and RSD 1.5% for DA), repeatability (RSD 2.25% for PAR and RSD 2.50% for DA) and high recovery (99.7% with an RSD of 1.3% for PAR

  5. An electrochemical sensor prepared by sonochemical one-pot synthesis of multi-walled carbon nanotube-supported cobalt nanoparticles for the simultaneous determination of paracetamol and dopamine

    Energy Technology Data Exchange (ETDEWEB)

    Kutluay, Aysegul; Aslanoglu, Mehmet, E-mail: maslanoglu@harran.edu.tr

    2014-08-11

    Highlights: • A GCE was modified with carbon nanotubes and cobalt nanoparticles. • The composite material was obtained using an ultrasonic chemical deposition method. • The CoNPs/MWCNT/GCE was applied for the simultaneous determination of PAR and DA. • The presence of AA and UA did not affect the responses of PAR and DA. • Lower detection limits were obtained using the CoNPs/MWCNT/GCE. - Abstract: Multi-walled carbon nanotubes (MWCNTs) functionalized by cobalt nanoparticles were obtained using a single step chemical deposition method in an ultrasonic bath. The composite material was characterized using scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDX). The electroactivity of the cobalt-functionalized MWCNTs was assessed in respect to the electrooxidation of paracetamol (PAR) and dopamine (DA). It was found that the carbon nanotube supported cobalt nanoparticles have significantly higher catalytic properties. The proposed electrode has been applied for the simultaneous determination of PAR and DA. The modified electrode could resolve the overlapped voltammetric waves of PAR and DA into two well-defined voltammetric peaks with peak to peak separation of about 203 mV. On the other hand, the presence of potential drug interfering compounds AA and UA did not affect the voltammetric responses of PAR and DA. The current of oxidation peaks showed a linear dependent on the concentrations of PAR and DA in the range of 5.2 × 10{sup −9}–4.5 × 10{sup −7} M (R{sup 2} = 0.9987) and 5.0 × 10{sup −8}–3.0 × 10{sup −6} M (R{sup 2} = 0.9999), respectively. The detection limits of 1.0 × 10{sup −9} M and 1.5 × 10{sup −8} M were obtained for PAR and DA, respectively. The proposed electrode showed good stability (peak current change: 4.9% with and RSD of 2.6% for PAR; 5.5% with and RSD of 3.0% for DA over 3 weeks), reproducibility (RSD 2.3% for PAR and RSD 1.5% for DA), repeatability (RSD 2.25% for PAR and RSD 2.50% for DA) and

  6. 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.

  7. 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

  8. Cobalt magnetic nanoparticles embedded in carbon matrix: biofunctional validation

    International Nuclear Information System (INIS)

    Carbon nanostructures and nanocomposites display versatile allotropic morphologies, physico-chemical properties and have a wide range of applications in mechanics, electronics, biotechnology, structural material, chemical processing, and energy management. In this study we report the synthesis, characterization, and biotechnological application of cobalt magnetic nanoparticles, with diameter approximately 15–40 nm, embedded in carbon structure (Co/C-MN). A single-step chemical process was used in the synthesis of the Co/C-MN. The Co/C-MN has presented superparamagnetic behavior at room temperature an essential property for immunoseparation assays carried out here. To stimulate interactions between proteins and Co/C-MN, this nanocomposite was functionalized with acrylic acid (AA). We have showed the bonding of different proteins onto Co/C-AA surface using immunofluorescence assay. A Co/C-AA coated with monoclonal antibody anti-pathogenic Leptospira spp. was able to capture leptospires, suggesting that it could be useful in immunoseparation assays.

  9. Cobalt magnetic nanoparticles embedded in carbon matrix: biofunctional validation

    Energy Technology Data Exchange (ETDEWEB)

    Krolow, Matheus Z., E-mail: matheuskrolow@ifsul.edu.br [Universidade Federal de Pelotas, Engenharia de Materiais, Centro de Desenvolvimento Tecnologico (Brazil); Monte, Leonardo G.; Remiao, Mariana H.; Hartleben, Claudia P.; Moreira, Angela N.; Dellagostin, Odir A. [Universidade Federal de Pelotas, Nucleo de Biotecnologia, Centro de Desenvolvimento Tecnologico (Brazil); Piva, Evandro [Universidade Federal de Pelotas, Faculdade de Odontologia (Brazil); Conceicao, Fabricio R. [Universidade Federal de Pelotas, Nucleo de Biotecnologia, Centro de Desenvolvimento Tecnologico (Brazil); Carreno, Neftali L. V. [Universidade Federal de Pelotas, Engenharia de Materiais, Centro de Desenvolvimento Tecnologico (Brazil)

    2012-09-15

    Carbon nanostructures and nanocomposites display versatile allotropic morphologies, physico-chemical properties and have a wide range of applications in mechanics, electronics, biotechnology, structural material, chemical processing, and energy management. In this study we report the synthesis, characterization, and biotechnological application of cobalt magnetic nanoparticles, with diameter approximately 15-40 nm, embedded in carbon structure (Co/C-MN). A single-step chemical process was used in the synthesis of the Co/C-MN. The Co/C-MN has presented superparamagnetic behavior at room temperature an essential property for immunoseparation assays carried out here. To stimulate interactions between proteins and Co/C-MN, this nanocomposite was functionalized with acrylic acid (AA). We have showed the bonding of different proteins onto Co/C-AA surface using immunofluorescence assay. A Co/C-AA coated with monoclonal antibody anti-pathogenic Leptospira spp. was able to capture leptospires, suggesting that it could be useful in immunoseparation assays.

  10. Large Scale Synthesis of Carbon Nanofibres on Sodium Chloride Support

    OpenAIRE

    Ravindra Rajarao; Badekai Ramachandra Bhat

    2012-01-01

    Large scale synthesis of carbon nanofibres (CNFs) on a sodium chloride support has been achieved. CNFs have been synthesized using metal oxalate (Ni, Co and Fe) as catalyst precursors at 680 C by chemical vapour deposition method. Upon pyrolysis, this catalyst precursors yield catalyst nanoparticles directly. The sodium chloride was used as a catalyst support, it was chosen because of its non‐toxic and water soluble nature. Problems, such as the detrimental effect of CNFs, the detrimental ef...

  11. Antimicrobial Activity of Carbon-Based Nanoparticles

    Directory of Open Access Journals (Sweden)

    Solmaz Maleki Dizaj

    2015-03-01

    Full Text Available Due to the vast and inappropriate use of the antibiotics, microorganisms have begun to develop resistance to the commonly used antimicrobial agents. So therefore, development of the new and effective antimicrobial agents seems to be necessary. According to some recent reports, carbon-based nanomaterials such as fullerenes, carbon nanotubes (CNTs (especially single-walled carbon nanotubes (SWCNTs and graphene oxide (GO nanoparticles show potent antimicrobial properties. In present review, we have briefly summarized the antimicrobial activity of carbon-based nanoparticles together with their mechanism of action. Reviewed literature show that the size of carbon nanoparticles plays an important role in the inactivation of the microorganisms. As major mechanism, direct contact of microorganisms with carbon nanostructures seriously affects their cellular membrane integrity, metabolic processes and morphology. The antimicrobial activity of carbon-based nanostructures may interestingly be investigated in the near future owing to their high surface/volume ratio, large inner volume and other unique chemical and physical properties. In addition, application of functionalized carbon nanomaterials as carriers for the ordinary antibiotics possibly will decrease the associated resistance, enhance their bioavailability and provide their targeted delivery.

  12. 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

  13. Synthesis of single-walled carbon nanotube networks using monodisperse metallic nanocatalysts encapsulated in reverse micelles

    OpenAIRE

    Gayduchenko Igor A.; Fedorov Georgy E.; Ibragimov Ramil A.; Stepanova Tatiana S.; Gazaliev Arsen S.; Vysochanskiy Nikolay A.; Bobrov Yuri A.; Malovichko Anton M.; Sosnin Ilya M.; Bobrinetskiy Ivan I.

    2016-01-01

    We report on a method of synthesis of single-walled carbon nanotubes percolated networks on silicon dioxide substrates using monodisperse Co and Ni catalyst. The catalytic nanoparticles were obtained by modified method of reverse micelles of bis-(2-ethylhexyl) sulfosuccinate sodium in isooctane solution that provides the nanoparticle size control in range of 1 to 5 nm. The metallic nanoparticles of Ni and Co were characterized using transmission electron mi...

  14. Supercritical CO 2 -philic nanoparticles suitable for determining the viability of carbon sequestration in shale

    KAUST Repository

    Xu, Yisheng

    2015-01-01

    © The Royal Society of Chemistry. A fracture spacing less than a decimeter is probably required for the successful sequestration of CO2 in shale. Tracer experiments using inert nanoparticles could determine if a fracturing this intense has been achieved. Here we describe the synthesis of supercritical CO2-philic nanoparticles suitable for this application. The nanoparticles are ~50 nm in diameter and consist of iron oxide (Fe3O4) and silica (SiO2) cores functionalized with a fluorescent polymeric corona. The nanoparticles stably disperse in supercritical carbon dioxide (scCO2) and are detectable to concentrations of 10 ppm. This journal is

  15. Assay of carbon nanoparticles in liquids.

    Science.gov (United States)

    Nawi, Yehuda; Sasson, Yoel; Dolgin, Bella

    2016-04-01

    The critical assay of carbon black concentration suffers from the lack of available methods, especially in-situ methods suitable for nanoparticles. We propose a useful tool for monitoring carbon nanoparticles concentration in liquids by means of RGB imaging, fluorescence and conductivity measurements. In this study carbon black particles of 25-75nm size were dispersed within two types of "green" liquids (1-butyl-3-methyl imidazolium based ionic liquids and glycerol) and the effect of carbon nanoparticles concentration on the liquids properties was measured. The conductivity of all the liquids increased with carbon concentration, while the slope of the curve was liquid dependent. The fluorescence intensity of ionic liquids decreased dramatically even when a small amount of carbon was added, while water-containing ionic liquids had a more moderate behavior. Glycerol has no native fluorescence, therefore, a known tracer present in soot (dibenzothiophene), having a characteristic fluorescence monitored by synchronous scan mode, was used. The carbon black effect on RGB imaging shows a linear dependence, while the red counts decreases with contamination. The proposed methods are simple and low-cost but nonetheless sensitive. PMID:26780588

  16. POROUS STRUCTURE OF CARBON NANOPARTICLES PREPARED BY CHLORINATION OF NANOPARTICLES OF SILICON CARBID

    OpenAIRE

    Sokolov, V. V.; PETROV N.A.; TOMKOVICH M.V.; GUSAROV V. V.

    2014-01-01

    Specific features of the structure of nanoporous carbon, prepared by chlorinating silicon carbide nanoparticles followed by treatment thereof by hydrogenation have been studied. A considerable number of microscopic pores in carbon nanoparticles have been shown.

  17. 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.

  18. Synthesis of Nanocrystalline Cellulose Stabilized Copper Nanoparticles

    OpenAIRE

    Aminu Musa; Ahmad, Mansor B.; Mohd Zobir Hussein; Saiman Mohd Izham; Kamyar Shameli; Hannatu Abubakar Sani

    2016-01-01

    A chemical reduction method was employed for the synthesis of copper nanoparticles stabilized by nanocrystalline cellulose (NCC) using different concentrations of copper salt in aqueous solution under atmospheric air. CuSO4·5H2O salt and hydrazine were used as metal ion precursor and reducing agent, respectively. Ascorbic acid and aqueous NaOH were also used as an antioxidant and a pH moderator, respectively. The number of CuNPs increased with increasing concentration of the precursor salt. T...

  19. Ag2CrO4 nanoparticles loaded on two-dimensional large surface area graphite-like carbon nitride sheets: simple synthesis and excellent photocatalytic performance.

    Science.gov (United States)

    Shi, Lei; Liang, Lin; Wang, Fangxiao; Liu, Mengshuai; Sun, Jianmin

    2016-04-01

    Graphite-like carbon nitride (g-C3N4) with a large surface area was prepared through thermal condensation of guanidine hydrochloride at 650 °C. Various amounts of silver chromate (Ag2CrO4) nanoparticles with small size were highly loaded on the g-C3N4 by a simple co-precipitation method at room temperature. The chemical constituents, surface structure and optical properties of the resultant Ag2CrO4/g-C3N4 composites were thoroughly characterized. And the photocatalytic performances were evaluated by degradation of Rhodamine B (RhB) and phenol, the experimental results indicated that the as-prepared Ag2CrO4/g-C3N4 composites presented excellent photocatalytic activity under visible-light irradiation. With the mass ratio of Ag2CrO4 to g-C3N4 at 1 : 2, the Ag2CrO4/g-C3N4 composites exhibited optimal photocatalytic activity for degrading RhB, approximately 6.1 and 10.4 times higher than those on pure g-C3N4 and bare Ag2CrO4 particles. The improved photocatalytic activity was mainly attributed to the combined effect including the larger surface area, highly dispersed smaller Ag2CrO4 nanoparticles, stronger visible absorption and higher charge separation efficiency of the Ag2CrO4/g-C3N4 composites. Moreover, the possible mechanism for the photocatalytic activity was tentatively proposed. PMID:26937621

  20. Attachment of Gold Nanoparticles to Carbon Nanotubes

    Institute of Scientific and Technical Information of China (English)

    Xi Cheng MA; Ning LUN; Shu Lin WEN

    2005-01-01

    Carbon nanotubes were initially chemically modified with an H2SO4-HNO3 treatment,and subsequently activated with Pd-Sn catalytic nuclei via a one-step activation approach. These activated nanotubes were used as precursors for obtaining gold nanoparticles-attached nanotubes via simple electroless plating. This approach provides an efficient method for attachment of metal nanostructures to carbon nanotubes. Such novel hybrid nanostructures are attractive for many applications.

  1. Synthesis and characterizations of CoPt nanoparticles supported on poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) functionalized multi-walled carbon nanotubes with superior activity for NaBH{sub 4} hydrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiao; Zhao, Yanchun, E-mail: yanchunzhao@aliyun.com; Peng, Xinglan; Wang, Jing; Jing, Chen; Tian, Jianniao, E-mail: birdtjn@sina.com

    2015-10-15

    Highlights: • Simple strategy for the synthesis of CoPt-PEDOT:PSS/MWCNTs. • PEDOT:PSS as a modifier of MWCNTs can improve the particles dispersion. • Superior catalytic activities for the NaBH{sub 4} hydrolysis reaction. - Abstract: We present here a facile strategy for synthesis of CoPt nanoparticles supported on poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS) functionalized multi-walled carbon nanotubes (MWCNTs). The as-prepared CoPt-PEDOT:PSS/MWCNT catalyst was characterized with UV–vis spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction and X-ray photoelectron. The well-supported and low-Pt-content nanostructure catalyst exhibits superior catalytic activity for the NaBH{sub 4} hydrolysis reaction with a 47.3 kJ mol{sup −1} of activation energy. The maximum hydrogen generation rate is 6900 mL min{sup −1} g{sup −1} at 298 K.

  2. Carbon doped ZnO: Synthesis, characterization and interpretation

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, D.K., E-mail: dilipiuac@gmail.com [Department of Physics, Institute of Technical Education and Research, Siksha ' O' Anusandhan University, Bhubaneswar 751030, Odisha (India); Mohapatra, J. [Department of Physics, Institute of Technical Education and Research, Siksha ' O' Anusandhan University, Bhubaneswar 751030, Odisha (India); Sharma, M.K.; Chattarjee, R. [Department of Physics, Indian Institute of Technology, IIT Delhi, Delhi 110016 (India); Singh, S.K. [Advanced Materials Technology Department, Institute of Minerals and Materials Technology (CSIR), Bhubaneswar 751013, Odisha (India); Varma, Shikha [Institute of Physics, Schivalaya Marg, Bhubaneswar 751004 (India); Behera, S.N. [School of Electrical Sciences, Indian Institute of Technology, IIT Bhubaneswar, Bhubaneswar 751013 (India); National Institute of Science and Technology (NIST), Berhampur 761008, Odisha (India); Nayak, Sanjeev K.; Entel, P. [Faculty of Physics and CeNiDE, University of Duisburg-Essen, 47057 Duisburg (Germany)

    2013-03-15

    A novel thermal plasma in-flight technique has been adopted to synthesize nanocrystalline ZnO and carbon doped nanocrystalline ZnO matrix. Transmission electron microscopy (TEM) studies on these samples show the average particle sizes to be around 32 nm for ZnO and for carbon doped ZnO. An enhancement of saturation magnetization in nanosized carbon doped ZnO matrix by a factor of 3.8 has been found in comparison to ZnO nanoparticles at room temperature. Raman measurement clearly indicates the presence of Zn-C complexes surrounded by ZnO matrix in carbon doped ZnO. This indicates that the ferromagnetic signature in carbon doped ZnO arises from the creation of defects or the development of oxy-carbon clusters, in the carbon doped ZnO system. Theoretical studies based on density functional theory also support the experimental analyses. - Highlights: Black-Right-Pointing-Pointer Synthesis of nanocrystalline ZnO and carbon doped ZnO matrix by inflight thermal plasma reactor. Black-Right-Pointing-Pointer Enhancement of ferromagnetism in nanosized carbon doped ZnO in comparison to ZnO nanoparticles. Black-Right-Pointing-Pointer Raman measurement indicates the presence of Zn-C complexes surrounded by ZnO matrix. Black-Right-Pointing-Pointer Ferromagnetic signature in carbon doped ZnO arises from the development of oxy-carbon clusters. Black-Right-Pointing-Pointer DFT supports experimental evidence of ferromagnetism in C doped ZnO nanoparticles.

  3. 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.

  4. Protein-mediated synthesis of gold nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ravindra, Pratibha [Department of Life Sciences, University of Mumbai, Kalina, Santacruz (E) 400098, Mumbai (India)], E-mail: Pratibha.kamble@osumc.edu

    2009-07-15

    Our current approach is to synthesize gold nanoparticles utilizing Serrapeptase that serves as both a reducing and stabilizing agent. The investigations further reveal that certain amino acid groups like lysine are involved in reduction and stabilization of these particles. The particles are characterized with UV-vis spectroscopy, Transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, Proton Nuclear Magnetic Resonance (H NMR) Spectroscopy studies and Sodium dodecyl sulphate-polyacrylamide gel electrophoresis for Serrapeptidase and Au-Serrapeptidase isolation. Transmission electron microscopy studies show particles ranging from 20 nm to 200 nm that are spherical, hexagonal and polygonal in nature. UV-vis spectroscopy shows surface plasmon band at 536 nm that indicates formation of spherical particles whereas, results further add that gold particles are formed inside the nanosphere that is stabilized by interaction of amino acid groups like {gamma}-lysine of peptase. Fourier transform infrared spectroscopy studies reveal that few carboxyl groups are involved during the synthesis process followed by stretching of -CH bonds which has been seen in the case of lysine of Serrapeptase. Current studies therefore show that the method utilized for the synthesis of Au-nanoparticles is a biofriendly method and the nanogold formed can be a useful attribute for various applications.

  5. Bio-Inspired Green Nanoparticles: Synthesis, Mechanism, and Antibacterial Application

    Science.gov (United States)

    Velusamy, Palaniyandi; Kumar, Govindarajan Venkat; Jeyanthi, Venkadapathi; Das, Jayabrata; Pachaiappan, Raman

    2016-01-01

    In the recent years, noble nanoparticles have attracted and emerged in the field of biology, medicine and electronics due to their incredible applications. There were several methods have been used for synthesis of nanoparticles such as toxic chemicals and high energy physical procedures. To overcome these, biological method has been used for the synthesis of various metal nanoparticles. Among the nanoparticles, silver nanoparticles (AgNPs) have received much attention in various fields, such as antimicrobial activity, therapeutics, bio-molecular detection, silver nanocoated medical devices and optical receptor. Moreover, the biological approach, in particular the usage of natural organisms has offered a reliable, simple, nontoxic and environmental friendly method. Hence, the current article is focused on the biological synthesis of silver nanoparticles and their application in the biomedical field. PMID:27123159

  6. 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...

  7. Synthesis and characterization of magnetic nanoparticles embedded in polyacrylonitrile nanofibers

    Science.gov (United States)

    Munteanu, Daniel; Ion, Rodica-Mariana; Cocina, George-Costel

    2010-11-01

    Nanomedicine is defined as the monitoring, repair, construction, and control of human biological systems at the molecular level using engineered nanodevices and nanostructures. Polyacrylonitrile (PAN) solution containing the iron oxide precursor iron (III) was electrospun and thermally treated to produce electrically conducting, magnetic carbon nanofiber mats with hierarchical pore structures. This paper discusses the synthesis of magnetite (Fe3O4) nanoparticles with mean crystallite size of 10 nm with polyacrylonitrile (PAN) as the protecting agent, creating nanofiber. The morphology and material properties of the resulting multifunctional nanofiber including the surface area were examined using various characterization techniques. Optical microscopy images show that uniform fibers were produced with a fiber diameter of ~600 nm, and this uniform fiber morphology is maintained after graphitization with a fiber diameter of ~330 nm. X-ray diffraction (XRD) studies reveal the size of Fe3O4 crystals. A combination of XRD and electron microscopy experiments reveals the formation of pores with graphitic nanoparticles in the walls as well as the formation of magnetite nanoparticles distributed throughout the fibers.

  8. Temperature driven transport of gold nanoparticles physisorbed inside carbon nanotubes

    DEFF Research Database (Denmark)

    Schoen, P.A.E.; Poulikakos, D.; Walther, Jens Honore; Koumoutsakos, P.

    2006-01-01

    We use molecular dynamics simulations to demonstrate the temperature driven mass transport of solid gold nanoparticles, physisorbed inside carbon nanotubes (CNTs). Our results indicate that the nanoparticle experiences a guided motion, in the direction opposite to the direction of the temperature...... affects the nanoparticle motion along the carbon lattice....

  9. Technology for microbial synthesis of nanoparticles

    International Nuclear Information System (INIS)

    Complete text of publication follows. Nanotechnology has a high potential to engineer and alter basic properties of materials, and to exploit unusual phenomena observed on the nanometer scale. Consequently, the development of nanomaterials is already involved in a vast range of application fields, however, most of their characteristics are still underexamined, and relevance of studies on their environmental fate, toxic effects and other health risks have just been recognized. Besides, environmental effects and high costs of present production technologies definitely outline a need of both competitive and eco-friendly alternatives. It is well known that microbial production of nanoparticles may offer new perspectives in the field of bionanotechnology since it provides clean, inexpensive and 'green chemistry' techniques, which are especially desired in the future when technology transfer to large-scale production is concerned. In the last years the development of biosynthetic methods was an exponentially growing field, which focused on nanoparticles of noble metals, elemental and composite semiconductors with diameters in the range of 5-100 nm. We initiated the set-up of a new laboratory for studying biosynthesis processes of nanoparticles. The primary goal of this project is to realize the ability of controlling the size of nanoparticles by the conditions of the synthesis, which is motivated by the fact that the optoelectronic and chemical properties are sensitively dependent on this single parameter in addition to their elemental composition. In general, the characterization of nanoparticles, as well as measurements of structural properties require the presence of dedicated analytical infrastructure. The local availability of techniques like TEM, SEM, EDX, XPS, EELS, SIMS/SNMS, AFS, ICP-MS and spectrophotometry provides an advantageous background to consolidate bionanotechnological programs in our institute. As a result of our first test experiments selenium

  10. 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...

  11. DNA binding and aggregation by carbon nanoparticles

    International Nuclear Information System (INIS)

    Significant environmental and health risks due to the increasing applications of engineered nanoparticles in medical and industrial activities have been concerned by many communities. The interactions between nanomaterials and genomes have been poorly studied so far. This study examined interactions of DNA with carbon nanoparticles (CNP) using atomic force microscopy (AFM). We experimentally assessed how CNP affect DNA molecule and bacterial growth of Escherichia coli. We found that CNP were bound to the DNA molecules during the DNA replication in vivo. The results revealed that the interaction of DNA with CNP resulted in DNA molecule binding and aggregation both in vivo and in vitro in a dose-dependent manner, and consequently inhabiting the E. coli growth. While this was a preliminary study, our results showed that this nanoparticle may have a significant impact on genomic activities.

  12. 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

  13. Microwave-assisted synthesis of magnetite nanoparticles for MR blood pool contrast agents

    International Nuclear Information System (INIS)

    Microwave-assisted polyol process was developed for the synthesis of magnetite nanoparticles with precisely controlled size, high crystallinity and high water solubility. The process is simple, time-saving and low energy-consuming due to the advantages of polyols and microwave irradiation combined. The crystal phases of the nanoparticles were determined by transmission electron microscopy, X-ray powder diffraction and Raman spectrum. The coating materials of the nanoparticles were analyzed by Fourier transformed infrared spectroscopy and thermal gravimetric analysis. Precise size tuning enables an easier way to adjust the relaxation properties of the magnetite nanoparticles. The colloid nanoparticles with high longitudinal relaxivity (r1) and low ratio of transverse relaxivity (r2) to r1 have a potential application in magnetic resonance angiography. - Highlights: → Microwave-assisted process was developed for the synthesis of magnetite nanoparticles. → Process is simple, time-saving and low energy-consuming. → Colloid nanoparticles have a potential application in magnetic resonance angiography. → Carbonate surface of nanoparticles facilitates for further modification.

  14. Microwave assisted one-step green synthesis of fluorescent carbon nanoparticles from ionic liquids and their application as novel fluorescence probe for quercetin determination

    International Nuclear Information System (INIS)

    In this study, a new sensitive and convenient method for the determination of quercetin based on the fluorescence quenching of fluorescent carbon nanoparticles (CNPs) was developed. The CNPs derived from ionic liquids were prepared using a green and rapid microwave-assisted synthetic approach for the first time. The one-step green preparation process is simple and effective, neither a strong acid solvent nor surface modification reagent is needed, which makes this approach very suitable for large-scale production. The prepared CNPs were characterized by high-resolution transmission electron microscopy, Fourier transform infrared spectrometry, elemental analysis and spectrofluorometry. In NH3–NH4Cl buffer solution (pH 9.47), the fluorescence signals of CNPs decreased obviously with increase of the quercetin concentration. The effect of other coexisting foreign substances on the intensity of CNPs showed a low interference response. Under the optimum conditions, the fluorescence intensity presented a linear response versus quercetin concentration according to the Stern–Volmer equation with an excellent 0.9989 correlation coefficient. The linearity ranged from 2.87×10−6 to 31.57×10−6 mol L−1 with the detection limit (3σ) of 9.88×10−8 mol L−1. The recovery of this method was in the range of 93.3–105.1%. Therefore, the CNPs could to be a promising candidate as a fluorescence probe for the detection of trace levels of quercetin due to their advantages in low-cost production, low cytotoxicity, strong fluorescence and excellent biocompatibility. -- Highlights: ► Fluorescent CNPs were synthesized with microwave pyrolysis approach. ► Ionic liquids were used as sources of carbon and nitrogen for the first time. ► The formation and functionalization of CNPs were accomplished simultaneously. ► CNPs were used as fluorescent probes for the determination of quercetin. ► A sensitive and convenient method based on the fluorescence quenching was developed

  15. Microwave assisted one-step green synthesis of fluorescent carbon nanoparticles from ionic liquids and their application as novel fluorescence probe for quercetin determination

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Deli; Yuan, Danhua [Department of Analytical Chemistry, China Pharmaceutical University, Nanjing 210009 (China); He, Hua, E-mail: dochehua@163.com [Department of Analytical Chemistry, China Pharmaceutical University, Nanjing 210009 (China); Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing 210009 (China); Gao, Mengmeng [Department of Analytical Chemistry, China Pharmaceutical University, Nanjing 210009 (China)

    2013-08-15

    In this study, a new sensitive and convenient method for the determination of quercetin based on the fluorescence quenching of fluorescent carbon nanoparticles (CNPs) was developed. The CNPs derived from ionic liquids were prepared using a green and rapid microwave-assisted synthetic approach for the first time. The one-step green preparation process is simple and effective, neither a strong acid solvent nor surface modification reagent is needed, which makes this approach very suitable for large-scale production. The prepared CNPs were characterized by high-resolution transmission electron microscopy, Fourier transform infrared spectrometry, elemental analysis and spectrofluorometry. In NH{sub 3}–NH{sub 4}Cl buffer solution (pH 9.47), the fluorescence signals of CNPs decreased obviously with increase of the quercetin concentration. The effect of other coexisting foreign substances on the intensity of CNPs showed a low interference response. Under the optimum conditions, the fluorescence intensity presented a linear response versus quercetin concentration according to the Stern–Volmer equation with an excellent 0.9989 correlation coefficient. The linearity ranged from 2.87×10{sup −6} to 31.57×10{sup −6} mol L{sup −1} with the detection limit (3σ) of 9.88×10{sup −8} mol L{sup −1}. The recovery of this method was in the range of 93.3–105.1%. Therefore, the CNPs could to be a promising candidate as a fluorescence probe for the detection of trace levels of quercetin due to their advantages in low-cost production, low cytotoxicity, strong fluorescence and excellent biocompatibility. -- Highlights: ► Fluorescent CNPs were synthesized with microwave pyrolysis approach. ► Ionic liquids were used as sources of carbon and nitrogen for the first time. ► The formation and functionalization of CNPs were accomplished simultaneously. ► CNPs were used as fluorescent probes for the determination of quercetin. ► A sensitive and convenient method based

  16. A novel and facile synthesis of carbon quantum dots via salep hydrothermal treatment as the silver nanoparticles support: Application to electroanalytical determination of H2O2 in fetal bovine serum.

    Science.gov (United States)

    Jahanbakhshi, Mojtaba; Habibi, Biuck

    2016-07-15

    A simple, low-cost, and green process was used for the synthesis of carbon quantum dots (CQDs) through the hydrothermal treatment of salep as a novel bio-polymeric carbon source in presence of only pure water. The silver nanoparticles (AgNPs) were embedded on the surface of CQDs by ultra-violate (UV) irradiation to the CQDs and silver nitrate mixture solution. The as-synthesized CQDs and AgNPs decorated CQDs nanohybrid (AgNPs/CQDs) were characterized by UV-vis and photoluminescence spectroscopy, Fourier transform-infrared spectroscopy, transmission electron microscopy, atomic force microcopy, X-ray diffraction, and field emission scanning electron microscopy. Then, the AgNPs/CQDs nanohybrid was casted on the glassy carbon electrode in order to prepare an amperometric hydrogen peroxide (H2O2) sensor. The electrochemical investigations show that the AgNPs/CQDs nanohybrid possesses an excellent performance toward the H2O2 reduction. In the optimum condition, the linear range of H2O2 determination was achieved from 0.2 to 27.0μM with high sensitivity (1.5μA/µM) and the limit of detection was obtained about 80nM (S/N=3). Finally, the prepared nanohybrid modified electrode was effectively applied to the H2O2 detection in the disinfected fetal bovine serum samples, and the recovery was obtained about 98%. The achieved results indicate that the AgNPs/CQDs nanohybrid with high reproducibility, repeatability, and stability has a favorable capability in electrochemical sensors improvement. PMID:26943787

  17. 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

  18. Controlled synthesis of Zn0 nanoparticles by bioreduction

    International Nuclear Information System (INIS)

    Synthesis of metallic Zn nanoparticles through bio-reduction methods is reported for the first time. The structure, shape and size of the nanoparticles are critically controlled through the pH used in the sample preparation. High resolution electron microscopy was used in order to determine the structure of individual nanoparticles. Formation of quantum dots and the efficiency of ion reduction in the synthesis process are studied through the optical absorption in colloids. The structure and stability of the Zn clusters (up to 4000 atoms) were determined through the calculation of minimum energy configurations using molecular and quantum mechanics approximations and image simulation. The structure of the obtained nanoparticles was preferentially hexagonal, although multiple twinned and fcc-like structures were identified. The size controlled synthesis of small nanoparticles in the quantum-dot range was demonstrated successfully

  19. 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.

  20. Epoxy based photoresist/carbon nanoparticle composites

    DEFF Research Database (Denmark)

    Lillemose, Michael; Gammelgaard, Lauge; Richter, Jacob;

    2008-01-01

    We have fabricated composites of SU-8 polymer and three different types of carbon nanoparticles (NPs) using ultrasonic mixing. Structures of composite thin films have been patterned on a characterization chip with standard UV photolithography. Using a four-point bending probe, a well defined stress...... is applied to the composite thin film and we have demonstrated that the composites are piezoresistive. Stable gauge factors of 5-9 have been measured, but we have also observed piezoresistive responses with gauge factors as high as 50. As SU-8 is much softer than silicon and the gauge factor of the...... composite material is relatively high, carbon nanoparticle doped SU-8 is a valid candidate for the piezoresistive readout in polymer based cantilever sensors, with potentially higher sensitivity than silicon based cantilevers....

  1. 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...

  2. Nanoparticle tracers in calcium carbonate porous media

    KAUST Repository

    Li, Yan Vivian

    2014-07-15

    Tracers are perhaps the most direct way of diagnosing subsurface fluid flow pathways for ground water decontamination and for natural gas and oil production. Nanoparticle tracers could be particularly effective because they do not diffuse away from the fractures or channels where flow occurs and thus take much less time to travel between two points. In combination with a chemical tracer they can measure the degree of flow concentration. A prerequisite for tracer applications is that the particles are not retained in the porous media as the result of aggregation or sticking to mineral surfaces. By screening eight nanoparticles (3-100 nm in diameter) for retention when passed through calcium carbonate packed laboratory columns in artificial oil field brine solutions of variable ionic strength we show that the nanoparticles with the least retention are 3 nm in diameter, nearly uncharged, and decorated with highly hydrophilic polymeric ligands. The details of these column experiments and the tri-modal distribution of zeta potential of the calcite sand particles in the brine used in our tests suggests that parts of the calcite surface have positive zeta potential and the retention of negatively charged nanoparticles occurs at these sites. Only neutral nanoparticles are immune to at least some retention. © 2014 Springer Science+Business Media.

  3. Designer synthesis of monodisperse heterodimer and ferrite nanoparticles

    OpenAIRE

    Nakhjavan, Bahar

    2011-01-01

    The work presented in this doctoral thesis is a facile procedure, thermal decomposition, forrnthe synthesis of different types of monodisperse heterodimer M@iron oxide (M= Cu, Co, Nirnand Pt) and single ferrites, MFe2O4 (M= Cu and Co), nanoparticles. In the following chapter,rnwe study the synthesis of these monodiperse nanoparticles with the similar iron precursorrn(iron pentacarbonyl) and different transition metal precursors such as metalrnacetate/acetylacetonate/formate precursors in the ...

  4. 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.

  5. Nanoparticles: synthesis and applications in life science and environmental technology

    International Nuclear Information System (INIS)

    This work focuses on the synthesis, functionalization, and application of gold and silver nanoparticles, magnetic nanoparticles Fe3O4, combination of 4-ATP-coated silver nanoparticles and Fe3O4 nanoparticles. The synthesis methods such as chemical reduction, seeding, coprecipitation,and inverse microemulsion will be outlined. Silica- and amino-coated nanoparticles are suitable for several applications in biomedicine and the environment. The applications of the prepared nanoparticles for early detection of breast cancer cells, basal cell carcinoma, antibacterial test, arsenic removal from water, Herpes DNA separation, CD4+ cell separation and isolation of DNA of Hepatitis virus type B (HBV) and Epstein–Barr virus (EBV) are discussed. Finally, some promising perspectives will be pointed out. (paper)

  6. 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

  7. Fungus mediated synthesis of biomedically important cerium oxide nanoparticles

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • First time biological synthesis of cerium oxide oxide nanoparticles using fungus Humicola sp. • Complete characterization of cerium oxide nanoparticles. • Biosynthesis of naturally protein capped, luminescent and water dispersible CeO2 nanoparticles. • Biosynthesized CeO2 nanoparticles can be used for many biomedical applications. - Abstract: Nanomaterials can be synthesized by chemical, physical and the more recently discovered biological routes. The biological routes are advantageous over the chemical and physical ones as unlike these, the biological synthesis protocols occur at ambient conditions, are cheap, non-toxic and eco-friendly. Although purely biological and bioinspired methods for the synthesis of nanomaterials are environmentally benign and energy conserving processes, their true potential has not been explored yet and attempts are being made to extend the formation of technologically important nanoparticles using microorganisms like fungi. Though there have been reports on the biosynthesis of oxide nanoparticles by our group in the past, no attempts have been made to employ fungi for the synthesis of nanoparticles of rare earth metals or lanthanides. Here we report for the first time, the bio-inspired synthesis of biomedically important cerium oxide (CeO2) nanoparticles using the thermophilic fungus Humicola sp. The fungus Humicola sp. when exposed to aqueous solutions of oxide precursor cerium (III) nitrate hexahydrate (CeN3O9·6H2O) results in the extracellular formation of CeO2 nanoparticles containing Ce (III) and Ce (IV) mixed oxidation states, confirmed by X-ray Photoemission Spectroscopy (XPS). The formed nanoparticles are naturally capped by proteins secreted by the fungus and thus do not agglomerate, are highly stable, water dispersible and are highly fluorescent as well. The biosynthesized nanoparticles were characterized by UV–vis spectroscopy, Photoluminescence spectroscopy (PL), Transmission

  8. 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.

  9. Phonon assisted thermophoretic motion of gold nanoparticles inside carbon nanotubes

    DEFF Research Database (Denmark)

    Schoen, Philipp A.E.; Walther, Jens Honore; Poulikakos, Dimos;

    2007-01-01

    The authors investigate the thermally driven mass transport of gold nanoparticles confined inside carbon nanotubes using molecular dynamics simulations. The observed thermophoretic motion of the gold nanoparticles correlates with the phonon dispersion exhibited by a standard carbon nanotube and, in...... particular, with the breathing mode of the tube. Additionally, the results show an increased static friction for gold nanoparticles confines inside a zig-zag carbon nanotube when increasing the size length of the nanoparticles. However, an unexpected, opposite trend is observed for the same nanoparticles...

  10. 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...

  11. 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...

  12. 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,...

  13. 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.

  14. 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.

  15. Sol-gel synthesis of Fe-Co nanoparticles and magnetization study

    Science.gov (United States)

    Nautiyal, Pranjal; Seikh, Md. Motin; Lebedev, Oleg I.; Kundu, Asish K.

    2015-03-01

    We report the synthesis of carbon encapsulated Fe-Co nanoparticles using conventional sol-gel route and its magnetization studies. The x-ray diffraction indicates the formation of the single phase body centered cubic alloy Fe-Co phase with cell parameter of 2.857 Å. Nanoparticles are highly crystalline and exhibit low index faceting as determined from high-resolution transmission electron microscopy (HRTEM) investigation. The observed orthogonal lattice planes with lattice distance of 2.86 Å are attributed to (100) and (010). HRTEM image confirms the cube like Fe-Co nanoparticles with core-shell structure of carbon encapsulation, composed of carbon and graphite materials. The magnetometry results of the carbon encapsulated alloy Fe-Co nanoparticles with core-shell structure designate as a ferromagnetically ordered soft magnet with coercive field of 890 Oe (at 5 K). The coercive field and magnetization value depend on the size of nanoparticles as well as the diamagnetic contribution of carbon encapsulation.

  16. Carbon encapsulated magnetic nanoparticles produced by hydrothermal reaction

    Institute of Scientific and Technical Information of China (English)

    Nong Yue He; Ya Fei Guo; Yan Deng; Zhi Fei Wang; Song Li; Hong Na Liu

    2007-01-01

    Carbon encapsulated magnetic nanoparticles (CEMNs) were synthesized by heating an aqueous glucose solution containing FeAu (Au coated Fe nanoparticles) nanoparticles at 160-180 ℃ for 2 h. This novel hydrothermal approach is not only simple but also provides the surface of CEMNs with functional groups like-OH. The formation of carbon encapsulated magnetic nanoparticles was not favored when using pure Fe nanoparticles as cores because of the oxidation of Fe nanoparticles by H2O during the reaction and,therefore, the surfaces of the naked Fe nanoparticles had to be coated by Au shell in advance. TEM, XRD, XPS and VSM measurments characterized that they were uniform carbon spheres containing some embedded Fe-Au nanoparticles, with a saturation of 14.6 emu/g and the size of the typical product is ~350 nm.

  17. Growth of carbon nanostructures on carbonized electrospun nanofibers with palladium nanoparticles

    International Nuclear Information System (INIS)

    This paper studies the mechanism of the formation of carbon nanostructures on carbon nanofibers with Pd nanoparticles by using different carbon sources. The carbon nanofibers with Pd nanoparticles were produced by carbonizing electrospun polyacrylonitrile (PAN) nanofibers including Pd(Ac)2. Such PAN-based carbon nanofibers were then used as substrates to grow hierarchical carbon nanostructures. Toluene, pyridine and chlorobenzine were employed as carbon sources for the carbon nanostructures. With the Pd nanoparticles embedded in the carbonized PAN nanofibers acting as catalysts, molecules of toluene, pyridine or chlorobenzine were decomposed into carbon species which were dissolved into the Pd nanoparticles and consequently grew into straight carbon nanotubes, Y-shaped carbon nanotubes or carbon nano-ribbons on the carbon nanofiber substrates. X-ray diffraction analysis and transmission electron microscopy (TEM) were utilized to capture the mechanism of formation of Pd nanoparticles, regular carbon nanotubes, Y-shaped carbon nanotubes and carbon nano-ribbons. It was observed that the Y-shaped carbon nanotubes and carbon nano-ribbons were formed on carbonized PAN nanofibers containing Pd-nanoparticle catalyst, and the carbon sources played a crucial role in the formation of different hierarchical carbon nanostructures

  18. High yield, facile aqueous synthesis and characterization of C18 functionalized iron oxide nanoparticles

    Science.gov (United States)

    Nair, Kishore Kumar; Kaur, Ranjeet; Iqbal, Nusrat; Hasan, Abshar; Alam, Samsul; Raza, S. K.

    2015-04-01

    The present study shows the synthesis of magnetite nanoparticles by co-precipitation method in three steps. The steps involve the precipitation of Fe3O4 nanoparticles followed by layer by layer functionalization with silica and tetraethoxy(octadyl)silane (C18). The prepared magnetite nanoparticles were investigated by SEM, TEM, XRD, FTIR and VSM. It was suggested that the intermediate iron oxide nanoparticles were formed by the competing processes of oxidation and crystal growth after decomposition of ferrous and ferric salts. The first step synthesized nanoparticles were of around 16 ± 4 nm, second step silica coating of 18 ± 3 nm and the final step C18 were of 56 ± 6 nm. The tetraethylorthosilicate hydrolyzed to form silicic acid which further polymerizes and thereby forms a layer of silica over magnetite nanoparticles. FTIR peaks at 2854 and 2921 cm-1 confirm the layering of C18 on silica encapsulated nanoparticles which corresponds to ˜CH2 and ˜(CH2)17CH3 carbon chain symmetric extension. The thickness of silica coating and C18 are 1.9 ± 0.3 nm and 38.6 ± 2.5 nm as confirmed from TEM size distribution curve. The saturation magnetism of magnetite, silica coated and C18 nanoparticles are 77.46, 74.53 and 68.76 emu g-1 respectively. Thus, Fe3O4, silica and C18 encapsulated magnetite nanoparticles were superparamagnetic.

  19. 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. PMID:25633046

  20. A Review of Methods for Synthesis of Al Nanoparticles

    Directory of Open Access Journals (Sweden)

    Hamid Reza Ghorbani

    2014-12-01

    Full Text Available The synthesis of metallic nanoparticles is an active area of academic and, more significantly, applied research in nanotechnology. Several methods have been introduced for the synthesis of these materials. The techniques for synthesizing aluminum nanoparticles can be divided into solid-phase, liquid-phase and gas-phase processes. The solid-phase techniques include mechanical ball milling and mechanochemical, the liquid-phase techniques include laser ablation, exploding wire, solution reduction, and decomposition process, whereas the gas-phase processes include gas evaporation, exploding wire, and laser ablation process. This study is an attempt to present an overview of Al nanoparticles preparation by various methods.

  1. Synthesis, characterization and toxicological evaluation of carbon-based nanostructures

    OpenAIRE

    Mendes, Rafael Gregorio

    2015-01-01

    The synthesis, characterization and biological evaluation of different graphene-based nanoparticles with potential biomedical applications are explored. The results presented within this work show that eukaryotic cells can respond differently not only to different types of nanoparticles, but also identify slight differences in the morphology of nanoparticles, such as size. This highlights the great importance of the synthesis and thorough characterization of nanoparticles in the design of eff...

  2. Synthesis and Characterization of Silver Nanoparticles for an Undergraduate Laboratory

    Science.gov (United States)

    Orbaek, Alvin W.; McHale, Mary M.; Barron, Andrew R.

    2015-01-01

    The aim of this simple, quick, and safe laboratory exercise is to provide undergraduate students an introduction to nanotechnology using nanoparticle (NP) synthesis. Students are provided two procedures that allow for the synthesis of different yet controlled sizes of silver NPs. After preparing the NPs, the students perform UV-visible…

  3. Actuators based on intrinsic conductive polymers/carbon nanoparticles nanocompositesElectroactive Polymer Actuators and Devices (EAPAD) 2013

    OpenAIRE

    Bocchini, Sergio; Ariano, Paolo; LOMBARDI, MARIANGELA; Accardo, Daisy

    2013-01-01

    New polyaniline (PANi) synthesis was performed starting from non-toxic N-phenil-p-phenylenediamine (aniline dimer) using reverse addition of monomer to oxidizing agent, the synthesis allows to produce highly soluble PANi. Several types of doped PANi were prepared to be used on electromechanical active actuators. Different techniques were used to include carbon nanoparticles such as carbon nanotubes and graphene. Bimorph solid state ionic actuators were prepared with these novel nanocomposites...

  4. Synthesis of hexagonal gold nanoparticles using a microfluidic reaction system

    International Nuclear Information System (INIS)

    A new microfluidic reaction system capable of mixing, transporting and reacting is developed for the synthesis of gold nanoparticles. It allows for a rapid and a cost-effective approach to accelerate the synthesis of gold nanoparticles. The microfluidic reaction chip is made from micro-electro-mechanical-system technologies which integrate a micro-mixer, micro-pumps, a micro-valve, micro-heaters and a micro temperature sensor on a single chip. Successful synthesis of dispersed gold nanoparticles has been demonstrated within a shorter period of time, as compared to traditional methods. It is experimentally found that precise control of the mixing/heating time for gold salts and reducing agents plays an essential role in the synthesis of gold nanoparticles. The growth process of hexagonal gold nanoparticles by a thermal aqueous approach is also systematically studied by using the same microfluidic reaction system. The development of the microfluidic reaction system could be promising for the synthesis of functional nanoparticles for future biomedical applications

  5. 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.

  6. Synthesis of Various Silica Nanoparticles for Foam Stability

    International Nuclear Information System (INIS)

    The synthesis of the non-porous silica nanoparticles with uniform sizes has been reported through the Sto ber method, the synthesis of meso porous silica nanoparticles with a specific morphology such as core-shell, rod-like, and hexagonal shapes is not so common. As a synthetic strategy for controlling the particle size, shape, and porosity, the synthesis of core-shell silicas with meso porous shells formed on silica particle cores through the self-assembly of silica precursor and organic templates or spherical meso porous silicas using modified Sto ber method was also reported. Recently, in an effort to reduce the amount of radioactive waste and enhance the decontamination efficiency during the decontamination process of nuclear facilities contaminated with radionuclides, a few research for the preparation of the decontamination foam containing solid nanoparticles has been reported. In this work, the silica nanoparticles with various sizes, shapes, and structures were synthesized based on the previous literatures. The resulting silica nanoparticles were used to investigate the effect of the nanoparticles on the foam stability. In a study on the foam stability using various silica nanoparticles, the results showed that the foam volume and liquid volume in foam was enhanced when using a smaller size and lower density of the silica nanoparticles. Silica nanoparticles with various sizes, shapes, and structures such as a non-porous, meso porous core-shell, and meso porous silica were synthesized to investigate the effect of the foam stability. The sizes and structural properties of the silica nanoparticles were easily controlled by varying the amount of silica precursor, surfactant, and ammonia solution as a basic catalyst. The foam prepared using various silica nanoparticles showed that foam the volume and liquid volume in the foam were enhanced when using a smaller size and lower density of the silica nanoparticles

  7. Synthesis of Various Silica Nanoparticles for Foam Stability

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Suk Bon; Yoon, Inho; Jung, Chonghun; Kim, Chorong; Choi, Wangkyu; Moon, Jeikwon [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2013-05-15

    The synthesis of the non-porous silica nanoparticles with uniform sizes has been reported through the Sto ber method, the synthesis of meso porous silica nanoparticles with a specific morphology such as core-shell, rod-like, and hexagonal shapes is not so common. As a synthetic strategy for controlling the particle size, shape, and porosity, the synthesis of core-shell silicas with meso porous shells formed on silica particle cores through the self-assembly of silica precursor and organic templates or spherical meso porous silicas using modified Sto ber method was also reported. Recently, in an effort to reduce the amount of radioactive waste and enhance the decontamination efficiency during the decontamination process of nuclear facilities contaminated with radionuclides, a few research for the preparation of the decontamination foam containing solid nanoparticles has been reported. In this work, the silica nanoparticles with various sizes, shapes, and structures were synthesized based on the previous literatures. The resulting silica nanoparticles were used to investigate the effect of the nanoparticles on the foam stability. In a study on the foam stability using various silica nanoparticles, the results showed that the foam volume and liquid volume in foam was enhanced when using a smaller size and lower density of the silica nanoparticles. Silica nanoparticles with various sizes, shapes, and structures such as a non-porous, meso porous core-shell, and meso porous silica were synthesized to investigate the effect of the foam stability. The sizes and structural properties of the silica nanoparticles were easily controlled by varying the amount of silica precursor, surfactant, and ammonia solution as a basic catalyst. The foam prepared using various silica nanoparticles showed that foam the volume and liquid volume in the foam were enhanced when using a smaller size and lower density of the silica nanoparticles.

  8. 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.

  9. 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.

  10. 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.

  11. 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

  12. Laser-induced synthesis of a nanostructured polymer-like metal-carbon complexes

    Science.gov (United States)

    Arakelian, S.; Kutrovskaya, S.; Kucherik, A.; Osipov, A.; Povolotckaia, A.; Povolotskiy, A.; Manshina, A.

    2016-04-01

    Synthesis of nanotructured metal-carbon materials by laser irradiation is an actual branch of laser physics and nanotechnology. Laser sources with different pulse duration allow changing the heating rate with realization of different transition scenarios and synthesis materials with various physical properties. We study the process of the formation of nanostructured metal-clusters and complexes using laser irradiation of colloidal systems which were consisted of carbon micro- nanoparticles and nanoparticles of noble metals. For carbon nanoparticles synthesis we use the method of laser ablation in liquid. For the realization of different regimes of laser surface modification of the target (glassycarbon and shungite) and the formation of micro- nanoparticles in a liquid the YAG:Nd laser with a pulse duration from 0.5 ms up to 20 ms (pulse energy up to 50J) was applied. We have used the CW-laser with moderate intensity in liquid (water or ethanol) for nanoparticle of noble metals synthesis. Thus, colloidal systems were obtained by using CW-laser with λ = 1.06 μm, I ~ 105-6 W/cm2, and t = 10 min. The average size of resulting particles was approximately about 10 to 100 nm. The nanoparticle obtaining was provided in the colloidal solution with different laser parameters. In this work we have investigated the mechanism of the metal-carbon cluster formation during the process of irradiation of colloidal system which were consisted of separate carbon, silver and gold nanoparticles. This system was irradiated by nanosecond laser (100 ns) with average power up to 50W.

  13. Impacts of Nickel Nanoparticles on Mineral Carbonation

    Directory of Open Access Journals (Sweden)

    Marius Bodor

    2014-01-01

    Full Text Available This work presents experimental results regarding the use of pure nickel nanoparticles (NiNP as a mineral carbonation additive. The aim was to confirm if the catalytic effect of NiNP, which has been reported to increase the dissolution of CO2 and the dissociation of carbonic acid in water, is capable of accelerating mineral carbonation processes. The impacts of NiNP on the CO2 mineralization by four alkaline materials (pure CaO and MgO, and AOD and CC steelmaking slags, on the product mineralogy, on the particle size distribution, and on the morphology of resulting materials were investigated. NiNP-containing solution was found to reach more acidic pH values upon CO2 bubbling, confirming a higher quantity of bicarbonate ions. This effect resulted in acceleration of mineral carbonation in the first fifteen minutes of reaction time when NiNP was present. After this initial stage, however, no benefit of NiNP addition was seen, resulting in very similar carbonation extents after one hour of reaction time. It was also found that increasing solids content decreased the benefit of NiNP, even in the early stages. These results suggest that NiNP has little contribution to mineral carbonation processes when the dissolution of alkaline earth metals is rate limiting.

  14. 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.

  15. Synthesis of Cu(2)ZnSnS(4) micro- and nanoparticles via a continuous-flow supercritical carbon dioxide process.

    Science.gov (United States)

    Casciato, Michael J; Levitin, Galit; Hess, Dennis W; Grover, Martha A

    2012-07-01

    CZTS: Atlanta. A supercritical CO(2) continuous-flow reactor is employed to deposit micro- and nanoparticles of copper zinc tin sulfide (CZTS), a promising material for thin-film solar cells, onto a silicon wafer. The image shows a chemical map of deposited CZTS particles (scale bar: 15 μm), and a Raman spectrum with a peak characteristic of CZTS. PMID:22707477

  16. Multilayered and complex nanoparticle architectures through plasma synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Phillips, Jonathan [Los Alamos National Laboratory; Wakeland, Stephen [UNM MECH.ENG.; Cui, Yuehua [UNM MECH.ENG.; Knapp, Angela [TOYOTA USA; Richard, Monique [TOYOTA USA; Luhrs, Claudia [UNM MECH.ENG.

    2009-01-01

    Using the Aerosol Through Plasma (ATP) method in conjunction with simple chemical techniques a variety of complex and novel nanoparticle architectures were created. A TP was used to make metal-core/carbon shell nanoparticles (ca. 50 nm diameter) of SnlCarbon and AI/Carbon. These have, respectively, potential for application as battery anode (for hybrid and electric vehicles) and high energy fuel In one example of post processing, the Sn-core/carbon-shell material is treated in acidic solution and yields a true nano-sized hollow carbon shell. These shells have potential application as catalyst supports, gas storage, a neutral buoyancy material for applications as varied as proppants, and slow release capsules for pharmaceutical or agricultural applications. A different set of post-A-T-P processes were used to make three layer nanoparticles with a metal core, graphite inner shell and ceramic outer shell. This method extends the range of achievable nanoparticles architectures, hence enabling new applications.

  17. Synthesis, characteristics and antimicrobial activity of ZnO nanoparticles

    Science.gov (United States)

    Janaki, A. Chinnammal; Sailatha, E.; Gunasekaran, S.

    2015-06-01

    The utilization of various plant resources for the bio synthesis of metallic nano particles is called green technology and it does not utilize any harmful protocols. Present study focuses on the green synthesis of ZnO nano particles by Zinc Carbonate and utilizing the bio-components of powder extract of dry ginger rhizome (Zingiber officinale). The ZnO nano crystallites of average size range of 23-26 nm have been synthesized by rapid, simple and eco friendly method. Zinc oxide nano particles were characterized by using X-ray diffraction (XRD), Scanning Electron Microscope (SEM), Energy Dispersive X-ray spectroscopy (EDX). FTIR spectra confirmed the adsorption of surfactant molecules at the surface of ZnO nanoparticles and the presence of ZnO bonding. Antimicrobial activity of ZnO nano particles was done by well diffusion method against pathogenic organisms like Klebsiella pneumonia, Staphylococcus aureus and Candida albicans and Penicillium notatum. It is observed that the ZnO synthesized in the process has the efficient antimicrobial activity.

  18. Carbon black directed synthesis of ultrahigh mesoporous carbon aerogels

    OpenAIRE

    Macías, Carlos; Haro Remón, Marta; Rasines, Gloria; Parra Soto, José Bernardo; Ovín Ania, María Concepción

    2013-01-01

    [EN] A simple modification of the conventional sol–gel polymerization of resorcinol–formaldehyde mixtures allowed a facile preparation of ultrahigh mesoporous carbon gels. In the conventional synthesis the growth of the cluster polymer particles leading to the development of the porosity is controlled by the R/C ratio. In the presence of a carbon conductive additive, the polymerization of the reactants proceeded through the formation of less-branched polymer clusters resulting in carbon gels ...

  19. Synthesis of Carbon Nanotube-Inorganic Hybrid Nanocomposites: An Instructional Experiment in Nanomaterials Chemistry

    Science.gov (United States)

    de Dios, Miguel; Salgueirino, Veronica; Perez-Lorenzo, Moises; Correa-Duarte, Miguel A.

    2012-01-01

    An experiment is described to introduce advanced undergraduate students to an exciting area of nanotechnology that incorporates nanoparticles onto carbon nanotubes to produce systems that have valuable technological applications. The synthesis of such material has been easily achieved through a simple three-step procedure. Students explore…

  20. Synthesis of silica/carbon-encapsulated core-shell spheres: templates for other unique core-shell structures and applications in in situ loading of noble-metal nanoparticles.

    Science.gov (United States)

    Wan, Yong; Min, Yu-Lin; Yu, Shu-Hong

    2008-05-01

    Silica@carbon core-shell spheres have been synthesized via a hydrothermal carbonization procedure with glucose as the carbon precursor and silica spheres as the cores. Such SiO(2)@C core-shell spheres can be further used as templates to produce SiO(2)@C@SiO(2), and SiO(2)@SiO(2) spheres with a vacant region in two SiO(2) shells, noble-metal nanoparticle loaded SiO(2)@C core-shell spheres, and hollow carbon capsules through different follow-up processes. The obtained core-shell materials possess remarkable chemical reactivity in reducing noble-metal ions to nanoparticles, e.g., platinum. These unique core-shell spherical composites could find applications in catalyst supports, adsorbents, encapsulation, nanoreactors, and reaction templates. PMID:18363416

  1. 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.

  2. 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.

  3. Phytochemical Synthesis and Preliminary Characterization of Silver Nanoparticles Using Hesperidin

    International Nuclear Information System (INIS)

    his paper is the first of its kind for development of rapid and ecofriendly method for synthesis of silver nanoparticles from aqueous solution of silver nitrate using the flavonoid “hesperidin” and optimization of the methodology. There is formation of stable spherical silver nanoparticles in the size range of 20–40nm. Optimization of methodology in terms of concentration of reactants and pH of the reaction mixture reduced the reaction time for silver nanoparticle formation to 2mins. Silver nanoparticles (AgNPs) were characterized by UV-Vis spectroscopy and transmission electron microscopy (TEM). UV-vis spectroscopy derived spectrum demonstrated a peak of 430nm which corresponds to the plasmon absorbance of silver nanoparticles. Transmission electron microscopy revealed spherical shaped silver nanoparticles in the size range of 20–40nm.

  4. 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.

  5. Alloy nanoparticle synthesis using ionizing radiation

    Science.gov (United States)

    Nenoff, Tina M.; Powers, Dana A.; Zhang, Zhenyuan

    2011-08-16

    A method of forming stable nanoparticles comprising substantially uniform alloys of metals. A high dose of ionizing radiation is used to generate high concentrations of solvated electrons and optionally radical reducing species that rapidly reduce a mixture of metal ion source species to form alloy nanoparticles. The method can make uniform alloy nanoparticles from normally immiscible metals by overcoming the thermodynamic limitations that would preferentially produce core-shell nanoparticles.

  6. 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.

  7. 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

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

    International Nuclear Information System (INIS)

    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 57Fe 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 Fe3−xO4 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

  9. Fe-inserted and shell-shaped carbon nanoparticles by cluster-mediated laser pyrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Fleaca, C.T., E-mail: claudiufleaca@yahoo.com [Laser Photochemistry Laboratory, National Institute for Lasers, Plasma and Radiation Physics (NILPRP), P.O. Box MG 36, R-077125 Bucharest-Magurele (Romania); Dumitrache, F.; Morjan, I.; Alexandrescu, R.; Sandu, I.; Luculescu, C.; Birjega, S. [Laser Photochemistry Laboratory, National Institute for Lasers, Plasma and Radiation Physics (NILPRP), P.O. Box MG 36, R-077125 Bucharest-Magurele (Romania); Prodan, G. [Ovidius University of Constanta, 124 Mamaia Bd., Constanta (Romania); Stamatin, I. [3 Nano-SAE Research Center, University of Bucharest, P.O. Box MG-38, R-077125 Bucharest-Magurele (Romania)

    2012-09-15

    Highlights: Black-Right-Pointing-Pointer Iron-inserted carbon nanoparticles were obtained by laser pyrolysis technique. Black-Right-Pointing-Pointer Two different structures (shell-shape and turbostratic) were found in the same experiment. Black-Right-Pointing-Pointer Increasing the pressure causes the increasing in carbon crystallinity/decreasing the Fe content. Black-Right-Pointing-Pointer Iron nanoinclusions are protected from oxidation by the carbon matrix. Black-Right-Pointing-Pointer Magnetism-related applications of these nanoparticles in life sciences are proposed. - Abstract: We report here the high-yield continuous synthesis of carbon nanoparticles with and without Fe content by laser pyrolysis technique. The laser beam decomposes (via C{sub 2}H{sub 4} sensitizer) the Fe(CO){sub 5} as Fe clusters which absorb themselves the laser radiation. They trigger the fast carbon particles formation by exothermic dehydrogenation/polymerization of the surrounded C{sub 2}H{sub 2} molecules. This combination between Fe clusters and C{sub 2}H{sub 2} generates nanoparticles with unusual structure. Depending on the gas pressure in the reaction chamber, two kinds of nanoparticles were obtained: at lower pressure, 30-40 nm diameter particles with a defective structure, part of them crowded with Fe clusters (3-6 nm) and two types of nanoparticles (around 50-60 nm) at the highest pressure. Some of them have a shell-shape structure, presenting a distinct envelope, other with a turbostratic arrangement, and few containing one or several smaller (3-20 nm) Fe nanoparticles trapped inside. We consider that these particular structures of our nanoparticles may be useful in applications such as MRI applications, drug delivery or catalysts.

  10. Method and electrochemical cell for synthesis and treatment of metal monolayer electrocatalysts metal, carbon, and oxide nanoparticles ion batch, or in continuous fashion

    Energy Technology Data Exchange (ETDEWEB)

    Adzic, Radoslav; Zhang, Junliang; Sasaki, Kotaro

    2015-04-28

    An apparatus and method for synthesis and treatment of electrocatalyst particles in batch or continuous fashion is provided. In one embodiment, the apparatus comprises a sonication bath and a two-compartment chamber submerged in the sonication bath. The upper and lower compartments are separated by a microporous material surface. The upper compartment comprises a cover and a working electrode (WE) connected to a Pt foil contact, with the foil contact connected to the microporous material. The upper chamber further comprises reference counter electrodes. The lower compartment comprises an electrochemical cell containing a solution of metal ions. In one embodiment, the method for synthesis of electrocatalysts comprises introducing a plurality of particles into the apparatus and applying sonication and an electrical potential to the microporous material connected to the WE. After the non-noble metal ions are deposited onto the particles, the non-noble metal ions are displaced by noble-metal ions by galvanic displacement.

  11. Synthesis of high purity metal oxide nanoparticles for optical applications

    Science.gov (United States)

    Baker, C.; Kim, W.; Friebele, E. J.; Villalobos, G.; Frantz, J.; Shaw, L. B.; Sadowski, B.; Fontana, J.; Dubinskii, M.; Zhang, J.; Sanghera, J.

    2014-09-01

    In this paper we present our recent research results in synthesizing various metal oxide nanoparticles for use as laser gain media (solid state as well as fiber lasers) and transparent ceramic windows via two separate techniques, co-precipitation and flame spray pyrolysis. The nanoparticles were pressed into ceramic discs that exhibited optical transmission approaching the theoretical limit and showed very high optical-to-optical lasing slope efficiency. We have also synthesized sesquioxide nanoparticles using a Flame Spray Pyrolysis (FSP) technique that leads to the synthesis of a metastable phase of sesquioxide which allows fabricating excellent optical quality transparent windows with very fine grain sizes. Finally, we present our research in the synthesis of rare earth doped boehmite nanoparticles where the rareearth ion is encased in a cage of aluminum and oxygen to prevent ion-ion proximity and energy transfer. The preforms have been drawn into fibers exhibiting long lifetimes and high laser efficiencies.

  12. Microfluidic Reactors for the Controlled Synthesis of Nanoparticles

    Science.gov (United States)

    Erdem, Emine Yegan

    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, concentration of reagents, residence times, etc. affect the structure of nanoparticles dramatically; therefore when the conditions vary locally in the reaction vessel, different sized nanoparticles form, causing polydispersity. In widely-used batch wise synthesis techniques, large sized reaction vessels are used to mix and heat reagents. In these types of systems, it is very hard to avoid thermal gradients and to achieve rapid mixing times as well as to control residence times. Also it is not possible to make rapid changes in the reaction parameters during the synthesis. The other drawback of conventional methods is that it is not possible to separate the nucleation of nanoparticles from their growth; this leads to combined nucleation and growth and subsequently results in polydisperse size distributions. Microfluidics is an alternative method by which the limitations of conventional techniques can be addressed. Due to the small size, it is possible to control temperature and concentration of reagents precisely as well as to make rapid changes in mixing ratios of reagents or temperature of the reaction zones. There have been several microfluidic reactors -- (microreactors) in literature that were designed to improve the size distribution of nanoparticles. In this work, two novel microfluidic systems were developed for achieving controlled synthesis of nanoparticles. The first microreactor was made out of a chemically robust polymer, polyurethane, and it was used for low

  13. Green Synthesis of Silver Nanoparticles from several NTFP Plants

    Directory of Open Access Journals (Sweden)

    Somnath BHOWMIK

    2016-03-01

    Full Text Available The biological synthesis of nanoparticles using plant extracts plays an important role in the field of nanotechnology. In this study, rapid, simple approach was applied for synthesis of silver nanoparticles using , Clerodendrum infortunatum, Mucuna interrupta, Phlogancanthus thyrsiflorus and Sansevieria trifasciata aqueous leaf extract. The plant extract acts both as reducing agent as well as capping agent. To identify the compounds responsible for reduction of silver ions, the functional groups present in plant extract were investigated by FTIR. Various techniques used to characterize synthesized nanoparticles are Scanning Electron Microscopy (SEM, Atomic Force Microscopy (AFM and UV–Visible spectrophotometer. Results confirmed that this protocol was simple, rapid, one step, eco-friendly, non-toxic and might be an alternative conventional physical/chemical methods. Conversion of silver nanoparticles takes place at room temperature without the involvement of any hazardous chemicals.

  14. Synthesis of carbon nanofibers on copper particles

    Science.gov (United States)

    Kol'tsova, T. S.; Larionova, T. V.; Shusharina, N. N.; Tolochko, O. V.

    2015-08-01

    We analyze the synthesis of carbon nanostructures from the gas phase (mixture of acetylene or ethylene with hydrogen) on the surface of copper particles without using other catalysts. The synthesized structures (multilayer graphene and carbon nanofibers) are analyzed by transmission electron microscopy and Raman scattering. It is shown that the fiber structure is determined by the C: H ratio in the gas phase. The kinetics of synthesis is analyzed in terms of the formal kinetics of conversion in accordance with the Johnson—Mehl—Avrami equation.

  15. One-pot solvothermal synthesis of graphene wrapped rice-like ferrous carbonate nanoparticles as anode materials for high energy lithium-ion batteries

    Science.gov (United States)

    Zhang, Fan; Zhang, Ruihan; Feng, Jinkui; Ci, Lijie; Xiong, Shenglin; Yang, Jian; Qian, Yitai; Li, Lifei

    2014-11-01

    Well dispersed rice-like FeCO3 nanoparticles were produced and combined with reduced graphene oxide (RGO) via a one-pot solvothermal route. SEM characterization shows that rice-like FeCO3 nanoparticles are homogeneously anchored on the surface of the graphene nanosheets; the addition of RGO is helpful to form a uniform morphology and reduce the particle size of FeCO3 to nano-grade. As anode materials for lithium-ion batteries, the FeCO3/RGO nanocomposites exhibit significantly improved lithium storage properties with a large reversible capacity of 1345 mA h g-1 for the first cycle and a capacity retention of 1224 mA h g-1 after 50 cycles with a good rate capability compared with pure FeCO3 particles. The superior electrochemical performance of the FeCO3/RGO nanocomposite electrode compared to the pure FeCO3 electrode can be attributed to the well dispersed RGO which enhances the electronic conductivity and accommodates the volume change during the conversion reactions. Our study shows that the FeCO3/RGO nanocomposite could be a suitable candidate for high capacity lithium-ion batteries.

  16. Synthesis of nano-particle and highly porous conducting perovskites from simple in situ sol–gel derived carbon templating process

    Indian Academy of Sciences (India)

    Wei Zhou; Ran Ran; Zongping Shao; Wanqin Jin; Nanping Xu

    2010-08-01

    Nano-sized La0.6Sr0.4Co0.2Fe0.8O$_{3–\\delta}$ (LSCF) and La0.8Sr0.2MnO$_{3–\\delta}$ (LSM) oxides were synthesized by a simple in situ sol–gel derived carbon templating process. Nano-sized LSCF–carbon and LSM–carbon composites were first obtained with a grain size of 20–30 nm. Further calcination of the obtained composites under air resulted in the nano-sized pure-phase perovskites with crystalline size of as small as 14 nm. Such a decrease in crystalline size of perovskite via the indirect calcination process was ascribed to the suppressing effect of carbon in the grain growth of perovskite. Furthermore, when the in situ created carbon was applied as a template for pore forming, a highly porous perovskite sintering body packing from the nano-sized perovskite oxide was obtained.

  17. 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...

  18. Template directed formation of nanoparticle decorated multi-walled carbon nanotube bundles with uniform diameter

    International Nuclear Information System (INIS)

    Bundles of multi-walled carbon nanotubes of uniform diameter decorated with Ni nanoparticles were synthesized using mesoporous silicates as templates. The ordered morphology and the narrow pore size distribution of mesoporous silicates provide an ideal platform to synthesize uniformly sized carbon nanotubes. In addition, homogeneous sub-10 nm pore sizes of the templates allow in situ formation of catalytic nanoparticles with uniform diameters which end up decorating the carbon nanotubes. The resulting carbon nanotubes are multi-walled with a uniform diameter corresponding to the pore diameter of the template used during the synthesis that are decorated with the catalysts used to synthesize them. They have a narrow size distribution which can be used in many energy related fields of research.

  19. Carbon nanotube synthesis from alcohols by a novel aerosol method

    International Nuclear Information System (INIS)

    Single- and multiwalled carbon nanotubes (CNTs) were synthesised by a novel aerosol method using alcohols, namely ethanol and octanol, as carbon precursors. Preformed iron and nickel aerosol nanoparticles, produced by evaporation from resistively heated metal wire, were used as catalysts. Multiwalled CNTs were initiated by 10 nm sized catalyst particles and produced in the presence of ethanol vapour with the partial pressure of 7072 Pa, while combination of 2.4 nm particles and decreased alcohol vapour pressure (123 Pa) resulted in the formation of mainly single-walled and a small fraction of double-walled CNTs. The effect of a promoter (thiophene) in the system was found to be very important for the synthesis of multiwalled CNTs, while only a 30% number concentration increase was found for the single-walled CNT production

  20. 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

  1. 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.

  2. Composite Materials with Magnetically Aligned Carbon Nanoparticles Having Enhanced Electrical Properties and Methods of Preparation

    Science.gov (United States)

    Hong, Haiping (Inventor); Peterson, G.P. (Bud) (Inventor); Salem, David R. (Inventor)

    2016-01-01

    Magnetically aligned carbon nanoparticle composites have enhanced electrical properties. The composites comprise carbon nanoparticles, a host material, magnetically sensitive nanoparticles and a surfactant. In addition to enhanced electrical properties, the composites can have enhanced mechanical and thermal properties.

  3. Electrochemical synthesis of Ag nanoparticles supported on glassy carbon electrode by means of p-isopropyl calix[6]arene matrix and its application for electrocatalytic reduction of H2O2

    International Nuclear Information System (INIS)

    The silver nanoparticles were prepared on the glassy carbon (GC) electrode, modified with p-iso propyl calix[6]arene, by preconcentration of silver ions in open circuit potential and followed by electrochemical reduction of silver ions. The stepwise fabrication process of Ag nanoparticles was characterized by scanning electron microscopy and electrochemical impedance spectroscopy. The prepared Ag nanoparticles were deposited with an average size of 70 nm and a homogeneous distribution on the surface of electrode. The observed results indicated that the presence of calixarene layer on the electrode surface can control the particle size and prevent the agglomeratione and electrochemical deposition is a promising technique for preparation of nanoparticles due to its easy-to-use procedure and low cost of implementation. Cyclic voltammetry experiments showed that Ag nanoparticles had a good catalytic ability for the reduction of hydrogen peroxide (H2O2). The effects of p-isopropyl calix[6]arene concentration, applied potential for reduction of Ag+, number of calixarene layers and pH value on the electrocatalytic ability of Ag nanoparticles were investigated. The present modified electrode exhibited a linear range from 5.0 × 10-5 to 6.5 × 10-3 M and a detection limit 2.7 × 10-5 M of H2O2 (S/N = 3) using amperometric method.

  4. Temperature driven transport of gold nanoparticles physisorbed inside carbon nanotubes

    DEFF Research Database (Denmark)

    Schoen, P.A.E.; Poulikakos, D.; Walther, Jens Honore;

    2006-01-01

    We use molecular dynamics simulations to demonstrate the temperature driven mass transport of solid gold nanoparticles, physisorbed inside carbon nanotubes (CNTs). Our results indicate that the nanoparticle experiences a guided motion, in the direction opposite to the direction of the temperature...... gradient applied to the carrier CNT. The force experienced by the nanoparticle is of thermophoretic character, scaling linearly with the applied temperature gradient. The present results prove that the surface corrugation of different types of CNTs and the magnitude of the temperature gradient strongly...... affects the nanoparticle motion along the carbon lattice....

  5. 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.

  6. 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

  7. 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.

  8. Synthesis, characterization, and antimicrobial properties of copper nanoparticles

    Science.gov (United States)

    Usman, Muhammad Sani; Zowalaty, Mohamed Ezzat El; Shameli, Kamyar; Zainuddin, Norhazlin; Salama, Mohamed; Ibrahim, Nor Azowa

    2013-01-01

    Copper nanoparticle synthesis has been gaining attention due to its availability. However, factors such as agglomeration and rapid oxidation have made it a difficult research area. In the present work, pure copper nanoparticles were prepared in the presence of a chitosan stabilizer through chemical means. The purity of the nanoparticles was authenticated using different characterization techniques, including ultraviolet visible spectroscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscopy. The antibacterial as well as antifungal activity of the nanoparticles were investigated using several microorganisms of interest, including methicillin-resistant Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa, Salmonella choleraesuis, and Candida albicans. The effect of a chitosan medium on growth of the microorganism was studied, and this was found to influence growth rate. The size of the copper nanoparticles obtained was in the range of 2–350 nm, depending on the concentration of the chitosan stabilizer. PMID:24293998

  9. 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

  10. Platinum-cobalt bimetallic nanoparticles in hollow carbon nanospheres for hydrogenolysis of 5-hydroxymethylfurfural

    Science.gov (United States)

    Wang, Guang-Hui; Hilgert, Jakob; Richter, Felix Herrmann; Wang, Feng; Bongard, Hans-Josef; Spliethoff, Bernd; Weidenthaler, Claudia; Schüth, Ferdi

    2014-03-01

    The synthesis of 2,5-dimethylfuran (DMF) from 5-hydroxymethylfurfural (HMF) is a highly attractive route to a renewable fuel. However, achieving high yields in this reaction is a substantial challenge. Here it is described how PtCo bimetallic nanoparticles with diameters of 3.6 ± 0.7 nm can solve this problem. Over PtCo catalysts the conversion of HMF was 100% within 10 min and the yield to DMF reached 98% after 2 h, which substantially exceeds the best results reported in the literature. Moreover, the synthetic method can be generalized to other bimetallic nanoparticles encapsulated in hollow carbon spheres.

  11. Streptomyces somaliensis mediated green synthesis of silver nanoparticles

    OpenAIRE

    Meysam Soltani Nejad; Mehrdad Khatami; Gholam Hosein Shahidi Bonjar

    2015-01-01

    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 ...

  12. Photochemical synthesis of colloidal gold nanoparticles

    International Nuclear Information System (INIS)

    Monodisperse gold nanoparticles protected by small organic molecules or by macromolecules with different sizes and shapes are widely used as a precursor material in various applications of gold nanotechnology. However, their preparation is still a formidable task. In this paper the use of photochemically assisted syntheses of monodisperse gold nanoparticles is summarized and some preparations by the authors' group are introduced. These include spherical and rod-like particles, bimetallic composite nanoparticles, and syntheses using complex intramolecular photoreduction to generate the reducing agent

  13. Continuous flow synthesis and characterization of tailor-made bare gold nanoparticles for use in SERS

    International Nuclear Information System (INIS)

    We describe a method for the synthesis of gold nanoparticles in a stainless steel continuous flow tubular reactor using tetrachloroauric acid as a precursor but without using a classical reducing agent. Gold(III) ion is reduced by stainless steel to form gold nanoparticles which are collected at the end of the coil. A single-phase system is introduced that generates dispersed nanoparticles in the absence of reducing agents on their surface. By controlling flow rates and temperature, the size of the nanoparticles can be tuned in the range from 24 nm to 36 nm. The reproducibility of the preparation was investigated, relative standard deviation of both the wavelength of the peak and the intensity of the plasmonic absorption band were determined and found to vary by 0.15 % and 6.5 %, respectively. Flow synthesis is found to be an excellent alternative to chemical methods to produce stable gold nanoparticles of varying size in an efficiently way. The particles obtained also perform very well when used as a substrate in surface enhanced Raman scattering as shown by the characterization of carboxylated single walled carbon nanotubes. (author)

  14. Synthesis and characterization of magnetite/PLGA/chitosan nanoparticles

    Science.gov (United States)

    Ibarra, Jaime; Melendres, Julio; Almada, Mario; Burboa, María G.; Taboada, Pablo; Juárez, Josué; Valdez, Miguel A.

    2015-09-01

    In this work, we report the synthesis and characterization of a new hybrid nanoparticles system performed by magnetite nanoparticles, loaded in a PLGA matrix, and stabilized by different concentrations of chitosan. Magnetite nanoparticles were hydrophobized with oleic acid and entrapped in a PLGA matrix by the emulsion solvent evaporation method, after that, magnetite/PLGA/chitosan nanoparticles were obtained by adding dropwise magnetite/PLGA nanoparticles in chitosan solutions. Magnetite/PLGA nanoparticles produced with different molar ratios did not show significant differences in size and the 3:1 molar ratio showed best spherical shapes as well as uniform particle size. Isothermal titration calorimetry studies demonstrated that the first stage of PLGA-chitosan interaction is mostly regulated by electrostatic forces. Based on a single set of identical sites model, we obtained for the average number of binding sites a value of 3.4, which can be considered as the number of chitosan chains per nanoparticle. This value was confirmed by using a model based on the DLVO theory and fitting zeta potential measurements of magnetite/PLGA/chitosan nanoparticles. From the adjusted parameters, we found that an average number of chitosan molecules of 3.6 per nanoparticle are attached onto the surface of the PLGA matrix. Finally, we evaluated the effect of surface charge of nanoparticles on a membrane model of endothelial cells performed by a mixture of three phospholipids at the air-water interface. Different isotherms and adsorption curves show that cationic surface of charged nanoparticles strongly interact with the phospholipids mixture and these results can be the basis of future experiments to understand the nanoparticles- cell membrane interaction.

  15. Non-carbon nanotubes: synthesis and simulation

    International Nuclear Information System (INIS)

    The discovery of a new allotropic form of carbon, extended nanometre-sized quasi-unidimensional tubular structures (carbon nanotubes), as well as broad prospects for the use of nanomaterials based on them initiated numerous studies in the search for, and design of, nanotubular structures based in other compounds. Some properties and the main methods for the synthesis of non-carbon nanotubes are considered. Studies on the simulation of the electronic structures of these unique objects are analysed. Results of experimental and theoretical studies along these lines are discussed. The bibliography includes 328 references.

  16. Non-carbon nanotubes: synthesis and simulation

    International Nuclear Information System (INIS)

    The discovery of a new allotropic form of carbon, extended nano-sized quasi-unidimensional tubular structures (carbon nanotubes) and the broad prospects for the use of nanomaterials based on them have initiated numerous studies on the search and design of nanotubular structures of other substances. Some properties and the main methods of synthesis of non-carbon nanotubes based in particular, on boron compounds molybdenum, tungsten, niobium chalcogenides and vanadium oxides are considered. The works on the simulation of the electronic structures of these unique objects are analysed. The results of experimental and theoretical studies along these lines are discussed

  17. Synthesis, characterization and potential applications of iron-platinum nanoparticles

    Science.gov (United States)

    Nandwana, Vikas

    Monodisperse FePt nanoparticles with controlled size and geometry have drawn great attention in the last decade for fundamental scientific studies and for their potential applications in advanced materials and devices such as ultra-high-density magnetic recording media, exchange-coupled nanocomposite magnets, biomedicines and nanodevices. This dissertation focuses on the synthesis and characterization of FePt nanoparticles and their use in potential applications. The FePt nanoparticles of different size (2 to 16 nm) and shape (spherical, cubic, rod) were synthesized by a chemical solution method. The size and shape of these particles were controlled by adjusting reaction parameters. The as-synthesized FePt nanoparticles have chemically disordered fcc structure and are superparamagnetic at room temperature. Upon heat treatment the nanoparticles were transformed into ordered L10 structure, and high coercivity up to 27 kOe was achieved. Magnetic properties of annealed FePt nanoparticles including magnetization and coercivity were strongly dependent on particle size, shape, composition and annealing temperature. FePt/Fe3O4 bimagnetic nanoparticles with two different morphologies, core/shell and heterodimer, were prepared by coating or attaching Fe3O4 on surface of FePt nanoparticles. The size of FePt and Fe3O4 was tuned very finely to obtain most effective exchange coupling. The heterodimer nanoparticles resulted in relatively poor magnetic properties compared to the core/shell nanoparticles due to insufficient exchange coupling. By optimizing the dimensions of the FePt and Fe3O 4 in core/shell bimagnetic nanoparticles, energy products up to 17.8 MGOe were achieved. FePt/Fe3O4 core/shell and FePt+Fe3O 4 mixed nanoparticles with similar magnetic properties were compacted under 2.0 GPa at 400°C, 500°C and 600°C. A density up to 84% of the full density was achieved. After annealing at 650°C in forming gas, the FePt/Fe3O4 compacted samples were converted into L10 Fe

  18. In situ synthesis of ceria nanoparticles in the ordered mesoporous carbon as a novel electrochemical sensor for the determination of hydrazine

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yue [College of Chemistry, Nankai University, 94 WeiJin Road, Tianjin 300071 (China); Li, Yijun, E-mail: yijunli@nankai.edu.cn [Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071 (China); College of Chemistry, Nankai University, 94 WeiJin Road, Tianjin 300071 (China); He, Xiwen [College of Chemistry, Nankai University, 94 WeiJin Road, Tianjin 300071 (China)

    2014-03-01

    Highlights: • CeO{sub 2}–OMC composites were prepared via a hydrothermal method. • CeO{sub 2}–OMC had electrocatalytic ability to oxidation of hydrazine. • The sensor had high sensitivity, excellent stability and reproducibility. • The sensor was successfully employed to detect hydrazine in real water samples. - Abstract: A novel ceria (CeO{sub 2})–ordered mesoporous carbon (OMC) modified electrode for the sensitive amperometric determination of hydrazine was reported. CeO{sub 2}–OMC composites were synthesized via a hydrothermal method at a relatively low temperature (180 °C) and characterized by scanning electron microscopy (SEM), transmission electron microcopy (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The CeO{sub 2}–OMC modified glassy carbon electrode was characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) and indicated good electrocatalytic effect to the oxidation of hydrazine. Under the optimized conditions, the present sensor could be used to measure hydrazine in wide linear range from 40 nM to 192 μM (R{sup 2} = 0.999) with a low detection limit of 12 nM (S/N = 3). Additionally, the sensor has been successfully applied to detect hydrazine in real water samples and the recoveries were between 98.2% and 105.6%. Eventually, the sensor exhibited an excellent stability and reproducibility as a promising method for determination of hydrazine.

  19. 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.

  20. 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.

  1. Self-Assembled Enzyme Nanoparticles for Carbon Dioxide Capture.

    Science.gov (United States)

    Shanbhag, Bhuvana Kamath; Liu, Boyin; Fu, Jing; Haritos, Victoria S; He, Lizhong

    2016-05-11

    Enzyme-based processes have shown promise as a sustainable alternative to amine-based processes for carbon dioxide capture. In this work, we have engineered carbonic anhydrase nanoparticles that retain 98% of hydratase activity in comparison to their free counterparts. Carbonic anhydrase was fused with a self-assembling peptide that facilitates the noncovalent assembly of the particle and together were recombinantly expressed from a single gene construct in Escherichia coli. The purified enzymes, when subjected to a reduced pH, form 50-200 nm nanoparticles. The CO2 capture capability of enzyme nanoparticles was demonstrated at ambient (22 ± 2 °C) and higher (50 °C) temperatures, under which the nanoparticles maintain their assembled state. The carrier-free enzymatic nanoparticles demonstrated here offer a new approach to stabilize and reuse enzymes in a simple and cost-effective manner. PMID:27109255

  2. 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

  3. Synthesis of silver nanoparticles using medicinal Zizyphus xylopyrus bark extract

    Science.gov (United States)

    Sumi Maria, Babu; Devadiga, Aishwarya; Shetty Kodialbail, Vidya; Saidutta, M. B.

    2015-08-01

    In the present paper, biosynthesis of silver nanoparticles using Zizyphus xylopyrus bark extract is reported. Z. xylopyrus bark extract is efficiently used for the biosynthesis of silver nanoparticles. UV-Visible spectroscopy showed surface plasmon resonance peaks in the range 413-420 nm confirming the formation of silver nanoparticles. Different factors affecting the synthesis of silver nanoparticles like methodology for the preparation of extract, concentration of silver nitrate solution used for biosynthesis and initial pH of the reaction mixture were studied. The extract prepared with 10 mM AgNO3 solution by reflux extraction method at optimum initial pH of 11, resulted in higher conversion of silver ions to silver nanoparticles as compared with those prepared by open heating or ultrasonication. SEM analysis showed that the biosynthesized nanoparticles are spherical in nature and ranged from 60 to 70 nm in size. EDX suggested that the silver nanoparticles must be capped by the organic components present in the plant extract. This simple process for the biosynthesis of silver nanoparticles using aqueous extract of Z. xylopyrus is a green technology without the usage of hazardous and toxic solvents and chemicals and hence is environment friendly. The process has several advantages with reference to cost, compatibility for its application in medical and drug delivery, as well as for large-scale commercial production.

  4. 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.

  5. 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)

  6. Synthesis, characterization, and antimicrobial properties of copper nanoparticles

    Directory of Open Access Journals (Sweden)

    Usman MS

    2013-11-01

    Full Text Available Muhammad Sani Usman,1 Mohamed Ezzat El Zowalaty,2,5 Kamyar Shameli,1,3 Norhazlin Zainuddin,1 Mohamed Salama,4 Nor Azowa Ibrahim1 1Department of Chemistry, Faculty of Science, 2Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, Universiti Putra Malaysia, Selangor, Malaysia; 3Materials and Energy, Research Center, Karaj, Iran; 4Faculty of Pharmacy, UiTM, Puncak Alam, Selangor, Malaysia; 5Department of Environmental Health, Faculty of Public Health and Tropical Medicine, Jazan University, Jazan, Kingdom of Saudi Arabia Abstract: Copper nanoparticle synthesis has been gaining attention due to its availability. However, factors such as agglomeration and rapid oxidation have made it a difficult research area. In the present work, pure copper nanoparticles were prepared in the presence of a chitosan stabilizer through chemical means. The purity of the nanoparticles was authenticated using different characterization techniques, including ultraviolet visible spectroscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscopy. The antibacterial as well as antifungal activity of the nanoparticles were investigated using several microorganisms of interest, including methicillin-resistant Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa, Salmonella choleraesuis, and Candida albicans. The effect of a chitosan medium on growth of the microorganism was studied, and this was found to influence growth rate. The size of the copper nanoparticles obtained was in the range of 2–350 nm, depending on the concentration of the chitosan stabilizer. Keywords: chitosan, copper nanoparticles, antimicrobial activity, chemical synthesis, aqueous medium

  7. A solvothermal method to synthesize fluorescent carbon nanoparticles and application to photocatalysis and electrocatalysis.

    Science.gov (United States)

    Hongren, Li; Feng, Li; Aimin, Deng

    2015-09-01

    A novel solvothermal approach to synthesize fluorescent carbon nanoparticles (CNPs) was developed using glucose and ammonium oxalate as the carbon source, and glycol as the solvent. The solution of as-prepared CNPs emitted blue-green fluorescence under ultraviolet (UV) light at 365 nm, and the carbon nanoparticle formation was investigated through XRD, TEM, DLS, FT-IR, UV, PL, XPS. The particle was well dispersed with an average diameter of about 10-30 nm. In contrast with previous methods, in this synthesis process neither strong acid treatment nor further surface modification was necessary. The solution of as-prepared CNPs were applied to photocatalytic degradation of mountain green in the present H2 O2 , and the decolorization rate was over 97% when the reaction time was more than 7 h under visible light. The as-prepared CNPs were also applied to electrocatalysis and showed excellent electrocatalytic activity. PMID:25408385

  8. 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.

  9. Palladium nanoparticles on hierarchical carbon surfaces: A new architecture for robust nano-catalysts

    Science.gov (United States)

    Vijwani, Hema; Mukhopadhyay, Sharmila M.

    2012-12-01

    Surface activity of heterogeneous catalysts can be enhanced if their sizes are reduced to nanometers. However, loose nanomaterials pose potential health and environmental risks. This issue has been addressed by attachment of palladium nanoparticles on multi-scale hierarchical carbon supports that have exceptionally high surface area per volume. The supports consist of porous carbon foam whose surface has been either chemically functionalized, or morphologically altered by grafting of carbon-nanotubes. It is seen that whereas chemical functionalization does provide some increase in nano-catalyst loading, morphological modification is significantly more powerful. It has the potential to create orders of magnitude increase in catalytic activity within the same overall volume. The synthesis techniques have been investigated in sufficient detail to provide significant control over the density and size of nanoparticles. Abundant distribution of nanoparticles is observed even within the deeper pores of the microcellular foam. The nanoparticles are seen to be metallic Pd having face centered cubic structure. Additionally, the nano-particles and nanotubes are durable, and remain attached to the base support after long periods of rapid rotation in water. These robust hybrid structures show promise in future applications such as sensors, water purification systems, fuel cell electrodes and hydrogen storage sponges.

  10. Polymer nanoparticles: shape-directed monomer-to-particle synthesis.

    Science.gov (United States)

    He, Tao; Adams, Dave J; Butler, Michael F; Cooper, Andrew I; Rannard, Steve P

    2009-02-01

    Well-defined dumbbell and tripartite organic nanoparticles (30-60 nm) were produced via a one-pot direct synthesis of branched amphiphilic block copolymers, avoiding the need for postsynthesis self-assembly steps. We show the mechanism of dumbbell formation is largely a concerted process of particle growth during polymerization, although data suggest that particle-particle linking also occurs, particularly at higher monomer conversions. Dumbbell particles formed using a disulfide bifunctional initiator lead to cleavable structures, underlining the role of initiator functionality in shape control and the potential for functionality placement. Trifunctional initiators allow the direct one-pot synthesis of "tripartite" clover-leaf shaped nanoparticles which would be difficult to achieve through conventional synthesis/self-assembly/cross-linking strategies. PMID:19133746

  11. 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.

  12. Laser-induced incandescence diagnostic for in situ monitoring of nanoparticle synthesis in an atmospheric plasma

    Science.gov (United States)

    Mitrani, James; Patel, Shane; Shneider, Mikhail; Stratton, Brent; Raitses, Yevgeny

    2014-10-01

    A DC arc discharge with a consumed graphite electrode is commonly used for synthesis of carbon nanoaparticles in a low temperature (0.1-1 eV), atmospheric pressure plasma. The formation of nanoparticles in this plasma is poorly understood; it is not clear where nanoparticles nucleate and grow in the arc discharge. Therefore, a laser-induced incandescence (LII) diagnostic for in situ monitoring of the nanoparticles' spatial distribution in the plasma is currently being constructed. The LII diagnostic involves heating the particles with a short-pulsed laser, and measuring the induced spatiotemporal incandescence profiles on longer timescales. By appropriately modeling the induced spatiotemporal incandescence profiles, one can measure particle diameters and volume fraction. LII diagnostics have been extensively used to study soot particles in flames. However, they have never been applied in a strongly coupled plasma background. Even though the spatial dimensions for soot and nanoparticles are similar, great care is needed in developing an LII diagnostic for monitoring nanoparticles in a plasma background. Therefore, we will calibrate our LII diagnostic by measuring spatiotemporal incandescence profiles of known, research grade soot and nanoparticles. This work was supported by DOE Contract DE-AC02-09CH11466.

  13. Synthesis of Silver Nanoparticles Using Hydroxyl Functionalized Ionic Liquids and Their Antimicrobial Activity

    Directory of Open Access Journals (Sweden)

    Young Key Shim

    2008-05-01

    Full Text Available We report a new one phase method for the synthesis of uniform monodisperse crystalline Ag nanoparticles in aqueous systems that has been developed by using newly synthesized mono and dihydroxylated ionic liquids and cationic surfactants based on 1,3-disubstituted imidazolium cations and halogens anions. The hydroxyl functionalized ionic liquids (HFILs and hydroxyl functionalized cationic surfactants (HFCSs also simultaneously acts both as the reductant and protective agent. By changing the carbon chain length, alcohol structure and anion of the 1,3-imidazolium based HFILs and HFCSs the particle size, uniform and dispersibility of nanoparticles in aqueous solvents could be controlled. Transmission electron microscopy (TEM, electron diffraction, UV-Vis and NMR, were used for characterization of HFILs, HFCSs and silver nanoparticles. TEM studies on the solution showed representative spherical silver nanoparticles with average sizes 2-8 nm, particularly 2.2 nm and 4.5 nm in size range and reasonable narrow particle size distributions (SD-standard distribution 0.2 nm and 0.5 nm respectively. The all metal nanoparticles are single crystals with face centered cubic (fcc structure. The silver nanoparticles surface of plasmon resonance band (λmax around 420 nm broadened and little moved to the long wavelength region that indicating the formation of silver nanoparticles dispersion with broad absorption around infrared (IR region. Silver complexes of these HFILs as well as different silver nanoparticles dispersions have been tested in vitro against several gram positive and gram negative bacteria and fungus. The silver nanoparticles providing environmentally friendly and high antimicrobial activity agents.

  14. Synthesis of copper nanoparticles in polycarbonate by ion implantation

    Indian Academy of Sciences (India)

    Annu Sharma; Suman Bahniwal; Sanjeev Aggarwal; S Chopra; D Kanjilal

    2011-07-01

    Copper nanoparticles have been synthesized in polycarbonate by 75 KeV Cu– ion implantation with various doses ranging from 6.4 × 1015 to 1.6 × 1017 ions/cm2 with a beam current density of 800 nA/cm2. The composites formed were structurally characterized using Ultraviolet-Visible (UV-Visible) absorption spectroscopy. The appearance of particle plasmon resonance peak, characteristic of copper nanoparticles at 603 nm in absorption spectra of polycarbonate implanted to a dose of 1.6 × 1017 ions/cm2, indicates towards the formation of copper nanoparticles in polycarbonate. Transmission electron microscopy further confirms the formation of copper nanoparticles having size ∼ 3.15 nm. The formation of copper nanoparticles in the layers carbonized by Cu– implantation has been discussed. The synthesized copper-polycarbonate nanocomposite has been found to be more conducting than polycarbonate as ascertained using current–voltage characteristics.

  15. 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.

  16. Synthesis of Nanoparticles using Atmospheric Microplasma Discharge

    International Nuclear Information System (INIS)

    Silver nanoparticles have been synthesized by the reduction of aqueous AgNO3 solution, with sucrose as a stabilizing agent, using Atmospheric Microplasma discharge (AMP). The microplasma caused the aqueous metal ions present in the solution to reduce and nucleate into nanoparticles at ambient conditions (room temperature and atmospheric pressure) without presence of any chemical reducing agents. Highly mono-dispersed silver nanoparticles were obtained and analyzed using FESEM, UV/Visible absorption and DLS (Dynamic Light Scattering). This AMP based nanofabrication offers a simple, fast, cost effective and an environment friendly technique for the fabrication of silver nanoparticles which in principle can be extended to the reduction of any cationic species through plasma-liquid coupling. (author)

  17. 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.

  18. Ultrasound-assisted synthesis and processing of carbon materials

    Science.gov (United States)

    Fortunato, Maria E.

    2011-12-01

    Part I: Porous carbons are of interest in many applications because of their high surface areas and other physicochemical properties, and much effort has been directed towards developing new methods for controlling the porosity of carbons. Ultrasonic spray pyrolysis (USP) is an aerosol method suitable for large-scale, continuous synthesis of materials. Ultrasound is used to create aerosol droplets of a precursor solution which serve as micron-sized spherical reactors for materials synthesis. This work presents a precursor system for the template-free USP synthesis of porous carbons using low-cost precursors that do not evolve or require hazardous chemicals: sucrose was used as the carbon source, and sodium carbonate, sodium bicarbonate, or sodium nitrate was added as a decomposition catalyst and porogen. The USP carbons had macroporous interiors and microporous shells with surface areas as high as 800 m2/g and a narrow pore size distribution. It was determined that the interior porosity was a result of the gas evolution from salt decomposition and not from the presence of a salt template. Porous carbon is frequently used as a catalyst support because it provides high surface area and it is chemically and physically stable under many anoxic reaction conditions. Typically, the preparation of supported catalysts requires multiple steps for carbonization and metal impregnation. In this work, iron-impregnated porous carbon microspheres (Fe-C) were prepared by a one-step USP process by incorporating both the carbon and metal sources into the precursor solution. Carbonization, pore formation, metal impregnation, and metal activation occurred simultaneously to produce Fe-C materials with surface areas as high as 800 m2/g and up to 10 wt% Fe incorporated as nanoparticles nanoparticles despite the fact that they are likely encapsulated in the porous carbon support. Part II: The effects of high intensity ultrasound arise from acoustic cavitation: the formation, growth, and

  19. 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.

  20. 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.

  1. Synthesis, characterization and optical properties of nanoparticles

    Science.gov (United States)

    Li, Shoutian

    ZnO, Si, silica, Ge, Ga oxide, W oxide and Mo oxide nanoparticles have been synthesized and characterized, and their optical properties have been investigated. These particles were synthesized by a Laser Vaporization and Controlled Condensation (LVCC) technique in a modified diffusion cloud chamber. The particles deposited on smooth substrates reveal highly organized web-like structures with uniform micrometer size pores. The effect of solvents on the web-like structures was also investigated. ZnO nanoparticles were also prepared by wet chemical methods such as the reversed micelle and sol solutions technique. The photoluminescence quantum yield is enhanced 10 times once the surfaces of the ZnO nanoparticles are coated with a layer of stearate molecules. Many techniques have been used to characterize the nanoparticles. SEM gives information about particle size and morphology; X-ray diffraction and Raman spectroscopy determine the crystallinity and crystal structure; XPS and FTIR reveal the surface chemical composition; UV-vis spectroscopy and photoluminescence measurements characterize the optical properties of nanoparticles. Silica nanoparticles, prepared in an amorphous phase, show bright blue photoluminescence upon irradiation with UV light, but the luminescence has a very short lifetime (less than 20 ns). Si nanoparticles, with a diamond-like crystal phase, acquire oxidized-surfaces on exposure to air. The surface-oxidized Si nanocrystals show a short- lived blue emission characteristic of the SiO2 coating and a longer-lived red emission at room temperature. The lifetime of the red emission depends on the emission wavelength. Some substituted benzene molecules and tungsten oxide nanoparticles can quench the red photoluminescence of the Si nanocrystals. Tungsten oxide and molybdenum oxide nanoparticles show photochromic properties: they change color to blue when irradiated. The photons drive a transition from one chemical state to another. The color change of

  2. Electromagnetically assisted synthesis of highly concentrated gold nanoparticle colloids

    Science.gov (United States)

    Hernandez, Laura; Rosas, Walter; Naranjo, Guillermo; Peralta, Xomalin G.; Vargas, Watson L.

    2015-03-01

    The synthesis of metallic nanoparticles is currently an extremely active area of research due to the multiple potential applications of nanomaterials to areas ranging from nano-medicine to catalysis. Some of the current challenges of nanoparticle synthesis protocols include synthesizing nanoparticles in high concentrations with a small polydispersity. The present study contrasts and compares the synthesis of highly concentrated colloidal gold using three different sources of electromagnetic radiation to assist the reaction. The first source was a Spectra Physics Mai Tai Ti:Sapphire laser made by Sperian, this laser generates 70 fs FWHM pulses with wavelengths in the range of 690-1040 nm. The second source was sun light; this was measured to have a power of 10W. The third source was a lowelDP lamp with a measured intensity of 25W. Both the solar light and the lamp's rays were concentrated using a 28cm x 28cm Fresnel lens. Results will be presented highlighting differences and similarities in size, shape, crystallinity and time of the reaction. We speculate about the role played by variations in wavelength, temporal profile of the electromagnetic source (pulsed vs. continuous), temperature of the reaction and excitation power in the final structure of the nanoparticles generated.

  3. Synthesis of fluoropolymers in supercritical carbon dioxide

    International Nuclear Information System (INIS)

    Fluoropolymers are used in many technologically demanding applications because of their balance of high-performance properties. A significant impediment to the synthesis of variants of commercially available amorphous fluoropolymers is their general insolubility in most solvents except chlorofluorocarbons (CFCs). The environmental concerns about CFCs can be circumvented by preparing these technologically important materials in supercritical fluids. The homogeneous solution polymerization of highly fluorinated acrylic monomers can be achieved in supercritical carbon dioxide by using free radical methods. In addition, detailed decomposition rates and efficiency factors were measured for azobisisobutyronitrile in supercritical carbon dioxide and were compared to those obtained with conventional liquid solvents

  4. Large Scale Synthesis of Carbon Nanofibres on Sodium Chloride Support

    Directory of Open Access Journals (Sweden)

    Ravindra Rajarao

    2012-06-01

    Full Text Available Large scale synthesis of carbon nanofibres (CNFs on a sodium chloride support has been achieved. CNFs have been synthesized using metal oxalate (Ni, Co and Fe as catalyst precursors at 680 C by chemical vapour deposition method. Upon pyrolysis, this catalyst precursors yield catalyst nanoparticles directly. The sodium chloride was used as a catalyst support, it was chosen because of its non‐toxic and water soluble nature. Problems, such as the detrimental effect of CNFs, the detrimental effects on the environment and even cost, have been avoided by using a water soluble support. The structure of products was characterized by scanning electron microscopy, transmission electron microscopy and Raman spectroscopy. The purity of the grown products and purified products were determined by the thermal analysis and X‐ray diffraction method. Here we report the 7600, 7000 and 6500 wt% yield of CNFs synthesized over nickel, cobalt and iron oxalate. The long, curved and worm shaped CNFs were obtained on Ni, Co and Fe catalysts respectively. The lengthy process of calcination and reduction for the preparation of catalysts is avoided in this method. This synthesis route is simple and economical, hence, it can be used for CNF synthesis in industries.

  5. Synthesis of amorphous silicon carbide nanoparticles in a low temperature low pressure plasma reactor.

    Science.gov (United States)

    Lin, Hongfei; Gerbec, Jeffrey A; Sushchikh, Michael; McFarland, Eric W

    2008-08-13

    Commercial scale production of silicon carbide (SiC) nanoparticles smaller than 10 nm remains a significant challenge. In this paper, a microwave plasma reactor and appropriate reaction conditions have been developed for the synthesis of amorphous SiC nanoparticles. This continuous gas phase process is amenable to large scale production use and utilizes the decomposition of tetramethylsilane (TMS) for both the silicon and the carbon source. The influence of synthesis parameters on the product characteristics was investigated. The as-prepared SiC particles with sizes between 4 and 6 nm were obtained from the TMS precursor in a plasma operated at low temperature and low precursor partial pressure (0.001-0.02 Torr) using argon as the carrier gas (3 Torr). The carbon:silicon ratio was tuned by the addition of hydrogen and characterized by x-ray photoelectron spectroscopy. The reaction mechanism of SiC nanoparticle formation in the microwave plasma was investigated by mass spectroscopy of the gaseous products. PMID:21828814

  6. Synthesis of amorphous silicon carbide nanoparticles in a low temperature low pressure plasma reactor

    International Nuclear Information System (INIS)

    Commercial scale production of silicon carbide (SiC) nanoparticles smaller than 10 nm remains a significant challenge. In this paper, a microwave plasma reactor and appropriate reaction conditions have been developed for the synthesis of amorphous SiC nanoparticles. This continuous gas phase process is amenable to large scale production use and utilizes the decomposition of tetramethylsilane (TMS) for both the silicon and the carbon source. The influence of synthesis parameters on the product characteristics was investigated. The as-prepared SiC particles with sizes between 4 and 6 nm were obtained from the TMS precursor in a plasma operated at low temperature and low precursor partial pressure (0.001-0.02 Torr) using argon as the carrier gas (3 Torr). The carbon:silicon ratio was tuned by the addition of hydrogen and characterized by x-ray photoelectron spectroscopy. The reaction mechanism of SiC nanoparticle formation in the microwave plasma was investigated by mass spectroscopy of the gaseous products

  7. 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.

  8. Radiolytic synthesis of carbon-supported PtRu nanoparticles using high-energy electron beam: effect of pH control on the PtRu mixing state and the methanol oxidation activity

    International Nuclear Information System (INIS)

    Electrode catalysts composed of carbon-supported PtRu nanoparticles (PtRu/C) for use as a direct methanol fuel cell anode were synthesized by the reduction of precursor ions in an aqueous solution via irradiation with a high-energy electron beam. The effect of pH control in the precursor solution on the PtRu mixing state and the methanol oxidation activity was studied in order to enhance the catalytic activity for methanol oxidation. The PtRu/C structures were characterized by transmission electron microscopy, inductively coupled plasma atomic emission spectrometry, X-ray fluorescence spectrometry, and X-ray diffraction and X-ray absorption fine structure techniques. The methanol oxidation activity was evaluated by linear sweep voltammetry. The initial pH of the precursor solution has little influence on the average grain size for the metal particles (approximately 3.5 nm) on the carbon particle supports, but the dispersibility of the metal particles, PtRu mixing state, and methanol oxidation activity differed. The maintenance of a low pH in the precursor solution gave the best dispersibility of the PtRu nanoparticles supported on the surface of the carbon particles, whereas, a high pH gave the best PtRu mixing state and the highest oxidation current although a low dispersibility of the PtRu nanoparticles supported on the surface of the carbon particles was obtained. The PtRu mixing state strongly correlated with the methanol oxidation current. In addition, a high pH was more effective for PtRu mixing when using an electron beam irradiation reduction method, because the complexation reaction of the chelating agents was improved, which resulted in an enhancement of the catalytic activity for methanol oxidation.

  9. 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

  10. Progress in electrochemical synthesis of magnetic iron oxide nanoparticles

    International Nuclear Information System (INIS)

    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

  11. 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.

  12. Composite of TiN nanoparticles and few-walled carbon nanotubes and its application to the electrocatalytic oxygen reduction reaction

    KAUST Repository

    Isogai, Shunsuke

    2011-11-30

    Nanoparticles meet nanotubes! Direct synthesis of TiN nanoparticles in a three-dimensional network of few-walled carbon nanotubes (FWCNTs) was achieved by using mesoporous graphitic carbon nitride (C 3N 4) as both a hard template and a nitrogen source. The TiN/FWCNT composite showed high performance for the oxygen reduction reaction in acidic media. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Monodisperse Mesoporous Carbon Nanoparticles from Polymer/Silica Self-Aggregates and Their Electrocatalytic Activities.

    Science.gov (United States)

    Huang, Xiaoxi; Zhou, Li-Jing; Voiry, Damien; Chhowalla, Manish; Zou, Xiaoxin; Asefa, Tewodros

    2016-07-27

    In our quest to make various chemical processes sustainable, the development of facile synthetic routes and inexpensive catalysts can play a central role. Herein we report the synthesis of monodisperse, polyaniline (PANI)-derived mesoporous carbon nanoparticles (PAMCs) that can serve as efficient metal-free electrocatalysts for the hydrogen peroxide reduction reaction (HPRR) as well as the oxygen reduction reaction (ORR) in fuel cells. The materials are synthesized by polymerization of aniline with the aid of (NH4)2S2O8 as oxidant and colloidal silica nanoparticles as templates, then carbonization of the resulting PANI/silica composite material at different high temperatures, and finally removal of the silica templates from the carbonized products. The PAMC materials that are synthesized under optimized synthetic conditions possess monodisperse mesoporous carbon nanoparticles with an average size of 128 ± 12 nm and an average pore size of ca. 12 nm. Compared with Co3O4, a commonly used electrocatalyst for HPRR, these materials show much better catalytic activity for this reaction. In addition, unlike Co3O4, the PAMCs remain relatively stable during the reaction, under both basic and acidic conditions. The nanoparticles also show good electrocatalytic activity toward ORR. Based on the experimental results, PAMCs' excellent electrocatalytic activity is attributed partly to their heteroatom dopants and/or intrinsic defect sites created by vacancies in their structures and partly to their high porosity and surface area. The reported synthetic method is equally applicable to other polymeric precursors (e.g., polypyrrole (PPY)), which also produces monodisperse, mesoporous carbon nanoparticles in the same way. The resulting materials are potentially useful not only for electrocatalysis of HPRR and ORR in fuel cells but also for other applications where high surface area, small sized, nanostructured carbon materials are generally useful for (e.g., adsorption

  14. Carbon nanotubes/laser ablation gold nanoparticles composites

    International Nuclear Information System (INIS)

    The production of nanohybrids formed by oxidized multiwalled carbon nanotubes (MWCNTs) and nanoparticles, produced by pulsed laser ablation in liquids process, is described. The use of linkers, obtained by transformation of pyrene-1-butanol, is mandatory to generate an efficient and stable interaction between the two components. Transmission electron microscopy and X-ray photoelectron spectroscopy analysis showed the obtainment of the efficient coverage of the MWCNTs by nanoparticles composed by metal gold and, partially, by oxides. - Highlights: • Laser ablation is a used for the production of gold nanoparticle colloids • An efficient decoration of carbon nanotubes with nanoparticles is obtained through the use of a linker • This method allows an efficient and tunable preparation of carbon nanotube hybrids

  15. Synthesis and Characterization of Polymer-Templated Magnetic Nanoparticles

    Science.gov (United States)

    Tamakloe, Beatrice

    This research reports on the investigation into the synthesis and stabilization of iron oxide nanoparticles for theranostic applications using amine-epoxide polymers. Although theranostic agents such as magnetic nanoparticles have been designed and developed for a few decades, there is still more work that needs to be done with the type of materials that can be used to stabilize or functionalize these particles if they are to be used for applications such as drug delivery, imaging and hyperthermia. For in-vivo applications, it is crucial that organic coatings enclose the nanoparticles in order to prevent aggregation and facilitate efficient removal from the body as well as protect the body from toxic material. The objective of this thesis is to design polymer coated magnetite nanoparticles with polymers that are biocompatible and can stabilize the iron oxide nanoparticle to help create mono-dispersed particles in solution. It is desirable to also have these nanoparticles possess high magnetic susceptibility in response to an applied magnetic field. The co-precipitation method was selected because it is probably the simplest and most efficient chemical pathway to obtain magnetic nanoparticles. In literature, cationic polymers such as Polyethylenimine (PEI), which is the industry standard, have been used to stabilize IONPs because they can be used in magnetofections to deliver DNA or RNA. PEI however is known to interact very strongly with proteins and is cytotoxic, so as mentioned previously the Iron Oxide nanoparticles (IONPs) synthesized in this study were stabilized with amine-epoxide polymers because of the limitations of PEI. Four different amine-epoxide polymers which have good water solubility, biodegradability and less toxic than PEI were synthesized and used in the synthesis and stabilization of the magnetic nanoparticles and compared to PEI templated IONPs. These polymer-templated magnetic nanoparticles were also characterized by size, surface charge, Iron

  16. 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 ...

  17. 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.

  18. Mesoporous MEL, BEA, and FAU zeolite crystals obtained by in situ formation of carbon template over metal nanoparticles

    DEFF Research Database (Denmark)

    Abildstrøm, Jacob Oskar; Ali, Zahra Nasrudin; Mentzel, Uffe Vie;

    2016-01-01

    nanoparticles supported on silica, a carbon–silica composite is obtained and exploited as a combined carbon template/silica source for the zeolite synthesis. The mesoporous zeolite materials were all prepared by hydrothermal crystallization in alkaline media followed by removal of the carbon template by...

  19. Spontaneous synthesis of gold nanoparticles on gum arabic-modified iron oxide nanoparticles as a magnetically recoverable nanocatalyst

    OpenAIRE

    Wu, Chien-Chen; Chen, Dong-Hwang

    2012-01-01

    A novel magnetically recoverable Au nanocatalyst was fabricated by spontaneous green synthesis of Au nanoparticles on the surface of gum arabic-modified Fe3O4 nanoparticles. A layer of Au nanoparticles with thickness of about 2 nm was deposited on the surface of gum arabic-modified Fe3O4 nanoparticles, because gum arabic acted as a reducing agent and a stabilizing agent simultaneously. The resultant magnetically recoverable Au nanocatalyst exhibited good catalytic activity for the reduction o...

  20. Synthesis, Properties, and Applications of Low-Dimensional Carbon-Related Nano materials

    International Nuclear Information System (INIS)

    In recent years, many theoretical and experimental studies have been carried out to develop one of the most interesting aspects of the science and nano technology which is called carbon-related nano materials. The goal of this paper is to provide a review of some of the most exciting and important developments in the synthesis, properties, and applications of low-dimensional carbon nano materials. Carbon nano materials are formed in various structural features using several different processing methods. The synthesis techniques used to produce specific kinds of low-dimensional carbon nano materials such as zero-dimensional carbon nano materials (including fullerene, carbon-encapsulated metal nanoparticles, nano diamond, and onion-like carbons), one-dimensional carbon nano materials (including carbon nano fibers and carbon nano tubes), and two-dimensional carbon nano materials (including graphene and carbon nano walls) are discussed in this paper. Subsequently, the paper deals with an overview of the properties of the mainly important products as well as some important applications and the future outlooks of these advanced nano materials.

  1. 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 ...

  2. Synthesis of Silver Nanoparticles Using Triticum aestivum and Its Effect on Peroxide Catalytic Activity and Toxicology

    OpenAIRE

    Sharada Dagade; Pooja Chavan; Shobha Waghmode; Vidya Kalyankar

    2013-01-01

    The synthesis of stable silver nanoparticles using bioreduction method was investigated. Biological synthesis of silver nanoparticles using Triticum aestivum (khapali ghahu) extract was investigated. The effect of a specific variety of plants and how it affects the growth of silver nanoparticles was investigated in our work and it was polydispersed. UV-visible spectroscopy was used to monitor the formation of silver nanoparticles within 15 minutes. The peaks in XRD pattern are in good agreeme...

  3. 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...

  4. Carbon Nanotubes Synthesis Through Gamma Radiation

    Science.gov (United States)

    Tirado, Pablo; Garcia, Rafael; Montes, Jorge; Melendrez, Rodrigo; Barboza, Marcelino; Contreras, Oscar

    2015-03-01

    Carbon nanotubes show a great potential of applications since there discovery by Iijima in 1991[1] due to their numerous physical-chemical properties such as their high weight to strength relationship, which make them ideal to use in high resistance compound materials, and in many other applications[2] In this work, a novel method for the synthesis of carbon nanotubes is presented, starting from an ultra-thin sheet of graphite synthesized by the chemical vapor decomposition technique (CVD), using ultra high purity methane and hydrogen at 1200°C in a horizontal quartz reactor. For the synthesis of carbon nanotubes, the graphite sheets were exposed to different doses of radiation, with the objective of breaking the graphite bonds and form carbon nanotubes; a Gammacell equipment model 220 Excel was used for the purpose, which counts with a radiation source of cobalt 60, and a current radiation rate of 0.9 Gy/seconds. The time of exposure to radiation was varied in each sample, according to the desired dose of radiation in each case, afterwards the samples were characterized using the Raman spectroscopy and TEM microscopy techniques with the objective of observing the kind of nanotubes formed, their morphology and their number of defects. Results will be shown during the poster session.

  5. Synthesis of Copper Nanoparticles Using Mixture of Allylamine and Polyallylamine

    Directory of Open Access Journals (Sweden)

    Rubén Sierra-Ávila

    2015-01-01

    Full Text Available Copper nanoparticles (Cu-NPs with sizes lower than 31 nm were prepared by wet chemical reduction using copper sulfate solution, hydrazine, and mixture of allylamine (AAm and polyallylamine (PAAm as stabilizing agents. The use of AAm/PAAm mixture leads to the formation of Cu and CuO nanoparticles. The resulting nanostructures were characterized by XRD, TGA, and TEM. The average particle diameters were determined by the Debye-Scherrer equation. Analysis by TGA, TEM, GS-MS, and 1HNMR reveals that synthesized NPs with AAm presented a coating with similar characteristics to NPs with PAAm, suggesting that AAm underwent polymerization during the synthesis. The synthesis of NPs using AAm could be a good alternative to reduce production costs.

  6. Synthesis and Application of Inorganic Nanoparticles as Lubricant Components - a Review

    International Nuclear Information System (INIS)

    Recent achievements in chemistry and technology of nanosized inorganic particles provide possibility of synthesis in various metal oxides, chalcogenides, and so on. Surface modification of nanoparticles in some cases provides formation of their stable dispersions in liquid hydrocarbons. State of art in the field of inorganic nanoparticles' synthesis and their application in tribology is discussed. Special attention is paid to synthesis of surface-capped and bare molybdenum sulfide nanoparticles and to testing thereof as friction-modifying additives for liquid lubricants. Differences in action mechanism of MoSx nanoparticles and 'molecular' molybdenum complexes are discussed. Future trends of inorganic nanoparticles use as lubricant additives are suggested

  7. 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

  8. 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...

  9. 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...

  10. 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.

  11. Synthesis of new dental nanocomposite with glass nanoparticles

    Directory of Open Access Journals (Sweden)

    Alireza Khavandi

    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.

  12. Probing carbon coatings on nanoparticle decorated carbon nanotubes by scanning transmission X-ray microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Li, Ming; Gao, Jing; Bai, Lili; Pu, Aiwu; Liu, Jinyin; Zhao, Guanqi; Sun, Xuhui; Zhong, Jun, E-mail: jzhong@suda.edu.cn

    2013-11-15

    Two kinds of carbon coating on carbon nanotubes (CNTs) after decoration with nanoparticles were observed by scanning transmission X-ray microscopy with a concurrent characterization of the electronic structure, revealing the complex compositions in CNTs after chemical modification. Moreover, a sandwich structure shown as CNT-nanoparticle-coating can be created with the exposure to X-ray for CNTs decorated with nanoparticle outside the wall. The coating shows an effective way for site-selective modification of CNTs with various carbon structures.

  13. 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.

  14. Microwave-assisted polyol synthesis of Cu nanoparticles

    International Nuclear Information System (INIS)

    Microwave heating was applied to synthesize copper colloidal nanoparticles by a polyol method that exploits the chelating and reducing power of a polidentate alcohol (diethylenglycol). The synthesis was carried out in the presence of eco-friendly additives such as ascorbic acid (reducing agent) and polyvinylpirrolidone (chelating polymer) to improve the reduction kinetics and sols stability. Prepared suspensions, obtained with very high reaction yield, were stable for months in spite of the high metal concentration. In order to optimize suspensions, synthesis parameters were modified and the effects on particle size, optical properties, and reaction yield were investigated. XRD analysis, scanning transmission electron microscopy (STEM), and DLS measurements confirmed that prepared sols consist of crystalline metallic copper with a diameter ranging from 45 to 130 nm. Surface plasmon resonance (SPR) of Cu nanoparticles was monitored by UV–Vis spectroscopy and showed both a red shift and a band weakening due to nanoparticle diameter increase. Microwave use provides rapid, uniform heating of reagents and solvent, while accelerating the reduction of metal precursors and the nucleation of metal clusters, resulting in monodispersed nanostructures. The proposed microwave-assisted synthesis, also usable in large-scale continuous production, makes process intensification possible.

  15. 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.

  16. 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.

  17. MOCVD Nanoparticle Synthesis from Copper Acetylacetonate

    Czech Academy of Sciences Publication Activity Database

    Moravec, Pavel; Smolík, Jiří; Klementová, Mariana; Levdansky, V.V.

    Thessaloniki : Hellenic Association for Aerosol Research, 2008, T01A058P. [European Aerosol Conference 2008. Thessaloniki (GR), 24.08.2008-29.08.2008] R&D Projects: GA ČR GA104/07/1093 Institutional research plan: CEZ:AV0Z40720504; CEZ:AV0Z40320502 Keywords : generation of nanoparticles * copper acetylacetonate * hot wall reactor Subject RIV: CF - Physical ; Theoretical Chemistry

  18. 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.

  19. 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...

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

    Science.gov (United States)

    Daniel, Weston Lewis

    limit for this ion in drinking water. Finally, Chapter 6 describes the synthesis of high density lipoprotein biomimetic nanoparticles capable of binding cholesterol. These structures use a gold nanoparticle core to template the assembly of a mixed phospholipid layer and the adsorption of apolipoprotein A-I. These synthesized structures have the general size and surface composition of natural HDL and bind free cholesterol with a Kd of 4 nM.

  1. A Review on the Respiratory System Toxicity of Carbon Nanoparticles

    OpenAIRE

    Maricica Pacurari; Kristine Lowe; Tchounwou, Paul B.; Ramzi Kafoury

    2016-01-01

    The respiratory system represents the main gateway for nanoparticles’ entry into the human body. Although there is a myriad of engineered nanoparticles, carbon nanoparticles/nanotubes (CNPs/CNTs) have received much attention mainly due to their light weight, very high surface area, durability, and their diverse applications. Since their discovery and manufacture over two decades ago, much has been learned about nanoparticles’ interactions with diverse biological system models. In particular, ...

  2. Photothermal Effects and Applications of Polydimethylsiloxane Membranes with Carbon Nanoparticles

    OpenAIRE

    Reinher Pimentel-Domínguez; Amado M. Velázquez-Benítez; J. Rodrigo Vélez-Cordero; Mathieu Hautefeuille; Francisco Sánchez-Arévalo; Juan Hernández-Cordero

    2016-01-01

    The advent of nanotechnology has triggered novel developments and applications for polymer-based membranes with embedded or coated nanoparticles. As an example, interaction of laser radiation with metallic and carbon nanoparticles has shown to provide optically triggered responses in otherwise transparent media. Incorporation of these materials inside polymers has led to generation of plasmonic and photothermal effects through the enhanced optical absorption of these polymer composites. In th...

  3. 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...

  4. 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.

  5. Nanoparticle Cookies Derived from Metal-Organic Frameworks: Controlled Synthesis and Application in Anode Materials for Lithium-Ion Batteries.

    Science.gov (United States)

    Wang, Shuhai; Chen, Minqi; Xie, Yanyu; Fan, Yanan; Wang, Dawei; Jiang, Ji-Jun; Li, Yongguang; Grützmacher, Hansjörg; Su, Cheng-Yong

    2016-05-01

    The capacity of anode materials plays a critical role in the performance of lithium-ion batteries. Using the nanocrystals of oxygen-free metal-organic framework ZIF-67 as precursor, a one-step calcination approach toward the controlled synthesis of CoO nanoparticle cookies with excellent anodic performances is developed in this work. The CoO nanoparticle cookies feature highly porous structure composed of small CoO nanoparticles (≈12 nm in diameter) and nitrogen-rich graphitic carbon matrix (≈18 at% in nitrogen content). Benefiting from such unique structure, the CoO nanoparticle cookies are capable of delivering superior specific capacity and cycling stability (1383 mA h g(-1) after 200 runs at 100 mA g(-1) ) over those of CoO and graphite. PMID:26948965

  6. 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)

  7. Assessment of carbon nanoparticle exposure on murine macrophage function

    Science.gov (United States)

    Suro-Maldonado, Raquel M.

    There is growing concern about the potential cytotoxicity of nanoparticles. Exposure to respirable ultrafine particles (2.5uM) can adversely affect human health and have been implicated with episodes of increased respiratory diseases such as asthma and allergies. Nanoparticles are of particular interest because of their ability to penetrate into the lung and potentially elicit health effects triggering immune responses. Nanoparticles are structures and devises with length scales in the 1 to 100-nanometer range. Black carbon (BC) nanoparticles have been observed to be products of combustion, especially flame combustion and multi-walled carbon nanotubes (MWCNT) have been shown to be found in both indoor and outdoor air. Furthermore, asbestos, which have been known to cause mesothelioma as well as lung cancer, have been shown to be structurally identical to MWCNTs. The aims of these studies were to examine the effects of carbon nanoparticles on murine macrophage function and clearance mechanisms. Macrophages are immune cells that function as the first line of defense against invading pathogens and are likely to be amongst the first cells affected by nanoparticles. Our research focused on two manufactured nanoparticles, MWCNT and BC. The two were tested against murine-derived macrophages in a chronic contact model. We hypothesized that long-term chronic exposure to carbon nanoparticles would decrease macrophages ability to effectively respond to immunological challenge. Production of nitric oxide (NO), tumor necrosis factor alpha (TNF-alpha), cell surface macrophage; activation markers, reactive oxygen species formation (ROS), and antigen processing and presentation were examined in response to lipopolysaccharide (LPS) following a 144hr exposure to the particulates. Data demonstrated an increase in TNF-alpha, and NO production; a decrease in phagocytosis and antigen processing and presentation; and a decrease in the expression levels of cell surface macrophage

  8. Nanoparticle Synthesis from Manganese(II) Acetylacetonate

    Czech Academy of Sciences Publication Activity Database

    Moravec, Pavel; Smolík, Jiří; Bakardjieva, Snejana; Levdansky, V.V.

    - : -, 2012, P281. [European Aerosol Confrernce EAC 2012. Granada (ES), 02.09.2012-07.09.2012] R&D Projects: GA ČR GA104/07/1093; GA ČR(CZ) GAP503/11/2315; GA ČR(CZ) GBP503/12/G147 Institutional support: RVO:67985858 Keywords : nanoparticle generation * metal organic CVD * hot wall tube reactor Subject RIV: CI - Industrial Chemistry, Chemical Engineering http://www.eac2012.com/EAC2012Book/3.html

  9. Synthesis of lead nanoparticles by Aspergillus species.

    Science.gov (United States)

    Pavani, K V; Kumar, N Sunil; Sangameswaran, B B

    2012-01-01

    In the context of the current demand to develop green technologies in material synthesis, a natural process in the synthesis of lead particles by Aspergillus species to suit such technology is reported. The fungal strain was grown in medium containing different concentrations of lead (0.2-1.5 mM) to determine its resistance to heavy metals. The organism was found to utilize some mechanism and accumulate lead particles outside and inside the cell. The extracellular presence of lead particles in the range of 1.77-5.8 microm was characterized by scanning electron microscopy. The presence of particles of lead in the 5-20 nm size range was found on the cell surface, in the periplasmic space and in the cytoplasm and was analyzed by transmission electron microscopy. PMID:22708348

  10. Synthesis of platinum nanoparticle electrocatalysts by atomic layer deposition

    Science.gov (United States)

    Lubers, Alia Marie

    Demand for energy continues to increase, and without alternatives to fossil fuel combustion the effects on our environment will become increasingly severe. Fuel cells offer a promising improvement on current methods of energy generation; they are able to convert hydrogen fuel into electricity with a theoretical efficiency of up to 83% and interface smoothly with renewable hydrogen production. Fuel cells can replace internal combustion engines in vehicles and are used in stationary applications to power homes and businesses. The efficiency of a fuel cell is maximized by its catalyst, which is often composed of platinum nanoparticles supported on carbon. Economical production of fuel cell catalysts will promote adoption of this technology. Atomic layer deposition (ALD) is a possible method for producing catalysts at a large scale when employed in a fluidized bed. ALD relies on sequential dosing of gas-phase precursors to grow a material layer by layer. We have synthesized platinum nanoparticles on a carbon particle support (Pt/C) by ALD for use in proton exchange membrane fuel cells (PEMFCs) and electrochemical hydrogen pumps. Platinum nanoparticles with different characteristics were deposited by changing two chemistries: the carbon substrate through functionalization; and the deposition process by use of either oxygen or hydrogen as ligand removing reactants. The metal depositing reactant was trimethyl(methylcyclopentadienyl)platinum(IV). Functionalizing the carbon substrate increased nucleation during deposition resulting in smaller and more dispersed nanoparticles. Use of hydrogen produced smaller nanoparticles than oxygen, due to a gentler hydrogenation reaction compared to using oxygen's destructive combustion reaction. Synthesized Pt/C materials were used as catalysts in an electrochemical hydrogen pump, a device used to separate hydrogen fuel from contaminants. Catalysts deposited by ALD on functionalized carbon using a hydrogen chemistry were the most

  11. Single-step synthesis of well-crystallized and pure barium titanate nanoparticles in supercritical fluids

    Science.gov (United States)

    Reverón, Helen; Aymonier, Cyril; Loppinet-Serani, Anne; Elissalde, Catherine; Maglione, Mario; Cansell, François

    2005-08-01

    Single-step synthesis of ultra-fine barium titanate powder with a crystallinity as high as 90% and without barium carbonate contamination has been successfully performed under supercritical conditions using a continuous-flow reactor in the temperature range 150-380 °C at 16 MPa. To synthesize this bimetallic oxide, alkoxides, ethanol and water were used. The influence of the synthesis parameters on the BaTiO3 powder characteristics was investigated. The results show that the water to alkoxide precursor ratio, the reactor temperature and the Ba:Ti molar ratio of alkoxide precursor play a major role in the crystallization of pure and well-crystallized BaTiO3 nanoparticles. The continuous mode of operation without post-treatments for powder washing, drying or crystallization increase the industrial interest.

  12. Synthesis of the Carbon Nanomaterials Based on Renewable Bioresources

    Directory of Open Access Journals (Sweden)

    N.A. Chan

    2014-07-01

    Full Text Available The effectiveness and feasibility of producing nanoscale carbon materials from renewable bioresources were shown as an example marsh mass. The mechanisms of synthesis of amorphous organic carbon from sphagnum moss species modified by a liquid peat phase of humic nature are discussed. A fundamentally new way of producing carbon nanotubes by mechanical activation of amorphous organic carbon is described.

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

    Energy Technology Data Exchange (ETDEWEB)

    Ghoreishi, S.M., E-mail: ghoreshi@cc.iut.ac.ir [Department of Chemical Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Nanotechnology and Advanced Materials Institute, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Meshkat, S.S. [Department of Chemical Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Department of Chemical Engineering, Urmia University of Technology, Urmia 57155-419 (Iran, Islamic Republic of); Ghiaci, M. [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Dadkhah, A.A. [Department of Chemical Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of)

    2012-06-15

    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 WS{sub 2} synthesis. ► WS{sub 2} 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. ► WS{sub 2} morphology could be controlled to obtain highly active and selective catalysts. ► Lower size of WS{sub 2} in this study overcomes the shortcoming of quartz reactor method. -- Abstract: The tungsten disulfide (WS{sub 2}) 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 (W{sub 0}), aging time and reagent concentration. The synthesized WS{sub 2} nanoparticles were characterized by zetasizer, UV–visible spectrophotometers and transmission electron microscopy (TEM). The WS{sub 2} 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 W{sub 0} increased the amount and particle size of WS{sub 2} 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 WS{sub 2} formation with 100% conversion of reactant ((NH{sub 4}){sub 2}WS{sub 4}) in the batch reactor.

  14. 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.

  15. Carbon-Carbon Cross Coupling Reactions in Ionic Liquids Catalysed by Palladium Metal Nanoparticles

    OpenAIRE

    Martin H. G. Prechtl; Scholten, Jackson D.; Jairton Dupont

    2010-01-01

    A brief summary of selected pioneering and mechanistic contributions in the field of carbon-carbon cross-coupling reactions with palladium nanoparticles (Pd-NPs) in ionic liquids (ILs) is presented. Five exemplary model systems using the Pd-NPs/ILs approach are presented: Heck, Suzuki, Stille, Sonogashira and Ullmann reactions which all have in common the use of ionic liquids as reaction media and the use of palladium nanoparticles as reservoir for the catalytically active palladium species.

  16. One step alkaline synthesis of biocompatible gold nanoparticles using dextrin as capping agent

    International Nuclear Information System (INIS)

    Gold nanoparticles (AuNPs) are used in sensing methods as tracers and transducers. The most common AuNP synthesis techniques utilize citrate under acidic reaction conditions. The synthesis described in this article generates glyco-AuNPs under mild alkaline conditions providing a “greener” alternative to Brust and Turkevich methodologies. This biologically compatible one-step technique uses dextrin as a capping agent and sodium carbonate as the reducing agent for chloroauric acid. The generated particles were relatively mono-dispersed and water soluble with a range of controllable mean diameters from 5.9 to 16.8 ± 1.6 nm. The produced AuNPs were stable in water for more than 6 months stored at room temperature (21 °C) in generation solution without protection from light. This article shows the effect of temperature, pH, and dextrin concentration on the synthesis procedure and AuNP diameter. These factors were found to control the reaction speed. The produced glyco-AuNPs were successfully functionalized with DNA oligonucleotides, and the functionalization efficiency was similar to citrate-generated AuNPs. The alkaline synthesis allows future exploration of simultaneous synthesis and functionalization procedures, which could significantly reduce the time of current ligand exchange methodologies.

  17. Carbon and oxide nanostructures. Synthesis, characterisation and applications

    Energy Technology Data Exchange (ETDEWEB)

    Yahya, Noorhana [Universiti Teknologi PETRONAS, Tronoh, Perak (Malaysia). Dept. of Fundamental and Applied Sciences

    2010-07-01

    This volume covers all aspects of carbon and oxide based nanostructured materials. The topics include synthesis, characterization and application of carbon-based namely carbon nanotubes, carbon nanofibres, fullerenes, carbon filled composites etc. In addition, metal oxides namely, ZnO, TiO2, Fe2O3, ferrites, garnets etc., for various applications like sensors, solar cells, transformers, antennas, catalysts, batteries, lubricants, are presented. The book also includes the modeling of oxide and carbon based nanomaterials. The book covers the topics: - Synthesis, characterization and application of carbon nanotubes, carbon nanofibres, fullerenes - Synthesis, characterization and application of oxide based nanomaterials. - Nanostructured magnetic and electric materials and their applications. - Nanostructured materials for petro-chemical industry. - Oxide and carbon based thin films for electronics and sustainable energy. - Theory, calculations and modeling of nanostructured materials. (orig.)

  18. 碳纳米管/ZnO纳米复合体的制备和表征%Synthesis and Characterization of a Nanocomplex of ZnO Nanoparticles Attached to Carbon Nanotubes

    Institute of Scientific and Technical Information of China (English)

    杨闵昊; 梁涛; 彭宇才; 陈清

    2007-01-01

    通过将不同直径的ZnO纳米颗粒与碳纳米管连接制备了碳纳米管/ZnO纳米复合体.将团聚的ZnO纳米颗粒分散并用表面活性剂CTAB使纳米颗粒带正电.化学氧化碳纳米管使其带负电.ZnO/CTAB微团通过碳管表面羧基与CTAB的静电作用与碳纳米管连接形成纳米复合体.研究了复合体形成的不同实验条件,表征了碳纳米管/ZnO纳米复合体的结构并研究了纳米复合体的光学特性.研究表明,与碳纳米管连接的ZnO纳米颗粒是互不连接的并保持量子点的特性.光致发光研究表明ZnO纳米颗粒的激发在纳米复合体中有淬灭.%A CNT/ZnO nanocomplex was fabricated by attaching ZnO nanoparticles with various diameters to carbon nanotubes (CNTs). The as-prepared agglomerate ZnO nanoparticles were dispersed and positively charged by utilizing a cationic surfactant cetyltrimethylammonium bromide (CTAB). ZnO/CTAB micelles were subsequently anchored to the surface of CNTs by electrostatic interaction between carboxyl groups on the chemically oxidized nanotubes' sidewalls and CTAB molecules. Different experimental conditions for the attachment were studied. The CNT/ZnO nanocomplex was characterized using structural and optical analysis methods. ZnO nanoparticles attached to the carbon nanotubes were found to be separated from each other maintaining characteristics of quantum dots Photoluminescence study showed that the emission of ZnO nanoparticles was quenched in the nanocomplex.

  19. Characterization and synthesis of carbon aggregates in high temperature environment

    OpenAIRE

    Russo, Carmela

    2013-01-01

    Carbon materials in all its forms, from the natural carbon solid materials, as coal and graphite, to the synthesized carbon materials, as carbon black, pitch fibers, fullerenes, carbon nanotubes, etc,. have been object of many studies regarding their characteristics and behaviour due to their importance in the energy and industrial sectors. Recently, most of the research efforts have been focused on the synthesis of new carbon materials and in particular on their physico-chemical propertie...

  20. Synthesis of Carbon Nanotube (CNT Composite Membranes

    Directory of Open Access Journals (Sweden)

    Dusan Losic

    2010-12-01

    Full Text Available Carbon nanotubes are attractive approach for designing of new membranes for advanced molecular separation because of their unique transport properties and ability to mimic biological protein channels. In this work the synthetic approach for fabrication of carbon nanotubes (CNTs composite membranes is presented. The method is based on growth of multi walled carbon nanotubes (MWCNT using chemical vapour deposition (CVD on the template of nanoporous alumina (PA membranes. The influence of experimental conditions including carbon precursor, temperature, deposition time, and PA template on CNT growth process and quality of fabricated membranes was investigated. The synthesis of CNT/PA composites with controllable nanotube dimensions such as diameters (30–150 nm, and thickness (5–100 µm, was demonstrated. The chemical composition and morphological characteristics of fabricated CNT/PA composite membranes were investigated by various characterisation techniques including scanning electron microscopy (SEM, energy-dispersive x-ray spectroscopy (EDXS, high resolution transmission electron microscopy (HRTEM and x-ray diffraction (XRD. Transport properties of prepared membranes were explored by diffusion of dye (Rose Bengal used as model of hydrophilic transport molecule.

  1. Highly efficient antibacterial iron oxide@carbon nanochains from wüstite precursor nanoparticles.

    Science.gov (United States)

    Situ, Shu F; Samia, Anna Cristina S

    2014-11-26

    A new hydrothermal synthesis approach involving the carbonization of glucose in the presence of wüstite (FeO) nanoparticles is presented, which leads to the fabrication of rapidly acting and potent antibacterial agents based on iron oxide@carbon (IO@C) nanochains. By using nonmagnetic FeO precursor nanoparticles that slowly oxidize into the magnetic Fe3O4 crystal structure under hydrothermal conditions, we were able to prepare well-defined and short-length IO@C nanochains that are highly dispersed in aqueous media and readily interact with bacterial cells, leading to a complete loss in bacterial cell viability within short incubation times at minimal dosage. The smaller IO@C nanochains synthesized using the FeO precursor nanoparticles can reach above 2-fold enhancement in microbe-killing activity when compared to the larger nanochains fabricated directly from Fe3O4 nanoparticles. In addition, the synthesized IO@C nanochains can be easily isolated using an external magnet and be subsequently recycled to effectively eradicate Escherichia coli cells even after five separate treatment cycles. PMID:25347201

  2. STUDY AN APPLICATION POSSIBILITY OF THE FLAVONOIDS FOR THE SYNTHESIS OF COPPER NANOPARTICLES

    OpenAIRE

    Mashxura A.Tagirova; Svetlana M. Vasina

    2015-01-01

    The method of biochemical synthesis of metals nanoparticles in inverse micelles using natural biologically active compounds, from flavonoids groups as reductants has been substantiated. An extraction of rutin from green tea and onion peel was carried out. Quantitative content of rutin in investigated objects was determined by photocolorimetric method. A synthesis of copper nanoparticles in inverse micelles by biochemical method has been carried out.

  3. 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.

  4. 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.

  5. 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.

  6. Adsorbent 2D and 3D carbon matrices with protected magnetic iron nanoparticles

    Science.gov (United States)

    Carreño, N. L. V.; Escote, M. T.; Valentini, A.; McCafferty, L.; Stolojan, V.; Beliatis, M.; Mills, C. A.; Rhodes, R.; Smith, C. T. G.; Silva, S. R. P.

    2015-10-01

    We report on the synthesis of two and three dimensional carbonaceous sponges produced directly from graphene oxide (GO) into which functionalized iron nanoparticles can be introduced to render it magnetic. This simple, low cost procedure, wherein an iron polymeric resin precursor is introduced into the carbon framework, results in carbon-based materials with specific surface areas of the order of 93 and 66 m2 g-1, compared to approx. 4 m2 g-1 for graphite, decorated with ferromagnetic iron nanoparticles giving coercivity fields postulated to be 216 and 98 Oe, values typical for ferrite magnets, for 3.2 and 13.5 wt% Fe respectively. The strongly magnetic iron nanoparticles are robustly anchored to the GO sheets by a layer of residual graphite, on the order of 5 nm, formed during the pyrolysis of the precursor material. The applicability of the carbon sponges is demonstrated in their ability to absorb, store and subsequently elute an organic dye, Rhodamine B, from water as required. It is possible to regenerate the carbon-iron hybrid material after adsorption by eluting the dye with a solvent to which it has a high affinity, such as ethanol. The use of a carbon framework opens the hybrid materials to further chemical functionalization, for enhanced chemical uptake of contaminants, or co-decoration with, for example, silver nanoparticles for bactericidal properties. Such analytical properties, combined with the material's magnetic character, offer solutions for environmental decontamination at land and sea, wastewater purification, solvent extraction, and for the concentration of dilute species.

  7. Adsorbent 2D and 3D carbon matrices with protected magnetic iron nanoparticles.

    Science.gov (United States)

    Carreño, N L V; Escote, M T; Valentini, A; McCafferty, L; Stolojan, V; Beliatis, M; Mills, C A; Rhodes, R; Smith, C T G; Silva, S R P

    2015-11-01

    We report on the synthesis of two and three dimensional carbonaceous sponges produced directly from graphene oxide (GO) into which functionalized iron nanoparticles can be introduced to render it magnetic. This simple, low cost procedure, wherein an iron polymeric resin precursor is introduced into the carbon framework, results in carbon-based materials with specific surface areas of the order of 93 and 66 m(2) g(-1), compared to approx. 4 m(2) g(-1) for graphite, decorated with ferromagnetic iron nanoparticles giving coercivity fields postulated to be 216 and 98 Oe, values typical for ferrite magnets, for 3.2 and 13.5 wt% Fe respectively. The strongly magnetic iron nanoparticles are robustly anchored to the GO sheets by a layer of residual graphite, on the order of 5 nm, formed during the pyrolysis of the precursor material. The applicability of the carbon sponges is demonstrated in their ability to absorb, store and subsequently elute an organic dye, Rhodamine B, from water as required. It is possible to regenerate the carbon-iron hybrid material after adsorption by eluting the dye with a solvent to which it has a high affinity, such as ethanol. The use of a carbon framework opens the hybrid materials to further chemical functionalization, for enhanced chemical uptake of contaminants, or co-decoration with, for example, silver nanoparticles for bactericidal properties. Such analytical properties, combined with the material's magnetic character, offer solutions for environmental decontamination at land and sea, wastewater purification, solvent extraction, and for the concentration of dilute species. PMID:26441224

  8. 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

  9. "Homeopathic" palladium nanoparticle catalysis of cross carbon-carbon coupling reactions.

    Science.gov (United States)

    Deraedt, Christophe; Astruc, Didier

    2014-02-18

    Catalysis by palladium derivatives is now one of the most important tools in organic synthesis. Whether researchers design palladium nanoparticles (NPs) or nanoparticles occur as palladium complexes decompose, these structures can serve as central precatalysts in common carbon-carbon bond formation. Palladium NPs are also valuable alternatives to molecular catalysts because they do not require costly and toxic ligands. In this Account, we review the role of "homeopathic" palladium catalysts in carbon-carbon coupling reactions. Seminal studies from the groups of Beletskaya, Reetz, and de Vries showed that palladium NPs can catalyze Heck and Suzuki-Miyaura reactions with aryl iodides and, in some cases, aryl bromides at part per million levels. As a result, researchers coined the term "homeopathic" palladium catalysis. Industry has developed large-scale applications of these transformations. In addition, chemists have used Crooks' concept of dendrimer encapsulation to set up efficient nanofilters for Suzuki-Miyaura and selective Heck catalysis, although these transformations required high PdNP loading. With arene-centered, ferrocenyl-terminated dendrimers containing triazolyl ligands in the tethers, we designed several generations of dendrimers to compare their catalytic efficiencies, varied the numbers of Pd atoms in the PdNPs, and examined encapsulation vs stabilization. The catalytic efficiencies achieved "homeopathic" (TON = 540 000) behavior no matter the PdNP size and stabilization type. The TON increased with decreasing the Pd/substrate ratio, which suggested a leaching mechanism. Recently, we showed that water-soluble arene-centered dendrimers with tri(ethylene glycol) (TEG) tethers stabilized PdNPs involving supramolecular dendritic assemblies because of the interpenetration of the TEG branches. Such PdNPs are stable and retain their "homeopathic" catalytic activities for Suzuki-Miyaura reactions for months. (TONs can reach 2.7 × 10(6) at 80 °C for aryl

  10. One-step hydrothermal synthesis of nitrogen-doped nanocarbons: albumine directing the carbonization of glucose.

    Science.gov (United States)

    Baccile, Niki; Antonietti, Markus; Titirici, Maria-Magdalena

    2010-02-22

    We present a simple and green one-step pathway towards nitrogen-doped carbon nanostructures with controlled mesoporosity through hydrothermal treatment of glucose in the presence of model proteins. Performing the reaction with different amounts of egg white ovalbumin protein (OvA), carbonaceous nanoparticles or continuous nanosponges with high specific surface areas can be efficiently produced. The nitrogen content of the structures is rather high (up to 8 wt%) and can be kept constant up to 950 degrees C, while oxygen elimination and graphitization of the carbon material occurs. We demonstrate here that sustainable natural resources can be efficiently used in the synthesis of pure high-potential nanomaterials. PMID:19885901

  11. 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.

  12. 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.

  13. 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.

  14. Radiochemical synthesis of 105gAg-labelled silver nanoparticles

    International Nuclear Information System (INIS)

    A method for synthesis of radiolabelled silver nanoparticles is reported. The method is based on proton activation of silver metal powder, enriched in 107Ag, with a 30.7 MeV proton beam. At this proton energy 105gAg is efficiently created, mainly via the 107Ag(p,3n)105Cd → 105gAg reaction. 105gAg has a half-life of 41.29 days and emits easily detectable gamma radiation on decay to 105Pd. 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 (AgNO3), 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 AgNO3 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

  15. Atomic Layer Deposition of Zirconium Oxide on Carbon Nanoparticles

    International Nuclear Information System (INIS)

    In this report we describe preparation of structures containing carbon nanoparticles for potential applications in nonvolatile memories. The carbon nanoparticles were synthesized from 5-methylresorcinol and formaldehyde via base catalysed polycondensation reaction, and were distributed over substrates by dip-coating the substrates into an organic solution. Before deposition of nanoparticles the substrates were covered with 2 nm thick Al2O3 layer grown by atomic layer deposition (ALD) from Al(CH3)3 and O3. After deposition of nanoparticles the samples were coated with ZrO2 films grown from C5H5Zr[N(CH3)2]3 and H2O. Both dielectrics were grown in two-temperature ALD processes starting deposition of Al2O3 at 25 °C and ZrO2 at 200 °C, thereafter completing both processes at a substrate temperature of 300 °C. Deposition of ZrO2 changed the structure of C-nanoparticles, which still remained in a Si/Al2O3/C/ZrO2 structure as a separate layer. Electrical characterization of nanostructures containing Al2O3 as tunnel oxide, C-nanoparticles as charge traps and ZrO2 as control oxide showed hysteretic flat-band voltage shift of about 1V

  16. Highly stable noble metal nanoparticles dispersible in biocompatible solvents: synthesis of cationic phosphonium gold nanoparticles in water and DMSO.

    Science.gov (United States)

    Ju-Nam, Yon; Abdussalam-Mohammed, Wanisa; Ojeda, Jesus J

    2016-04-12

    In this work, we report the synthesis of novel cationic phosphonium gold nanoparticles dispersible in water and dimethyl sulfoxide (DMSO) for their potential use in biomedical applications. All the cationic-functionalising ligands currently reported in the literature are ammonium-based species. Here, the synthesis and characterisation of an alternative system, based on phosphonioalkylthiosulfate zwitterions and phosphonioalkylthioacetate were carried out. We have also demonstrated that our phosphonioalkylthiosulfate zwitterions readily disproportionate into phosphonioalkylthiolates in situ during the synthesis of gold nanoparticles produced by the borohydride reduction of gold(iii) salts. The synthesis of the cationic gold nanoparticles using these phosphonium ligands was carried out in water and DMSO. UV-visible spectroscopic and TEM studies have shown that the phosphonioalkylthiolates bind to the surface of gold nanoparticles which are typically around 10 nm in diameter. The resulting cationic-functionalised gold nanoparticles are dispersible in aqueous media and in DMSO, which is the only organic solvent approved by the U.S. Food and Drug Administration (FDA) for drug carrier tests. This indicates their potential future use in biological applications. This work shows the synthesis of a new family of phosphonium-based ligands, which behave as cationic masked thiolate ligands in the functionalisation of gold nanoparticles. These highly stable colloidal cationic phosphonium gold nanoparticles dispersed in water and DMSO can offer a great opportunity for the design of novel biorecognition and drug delivery systems. PMID:26796782

  17. Nanoparticles of carbon allotropes inhibit glioblastoma multiforme angiogenesis in ovo

    Directory of Open Access Journals (Sweden)

    Grodzik M

    2011-11-01

    Full Text Available Marta Grodzik1, Ewa Sawosz1, Mateusz Wierzbicki1, Piotr Orlowski1, Anna Hotowy2, Tomasz Niemiec1, Maciej Szmidt3, Katarzyna Mitura4, André Chwalibog21Division of Biotechnology and Biochemistry of Nutrition, Warsaw University of Life Sciences, Warsaw, Poland; 2Department of Basic Animal and Veterinary Science, University of Copenhagen, Copenhagen, Denmark; 3Division of Histology and Embryology, Warsaw University of Life Sciences, Warsaw, Poland; 4Department of Biomedical Engineering, Koszalin University of Technology, Koszalin, PolandAbstract: The objective of the study was to determine the effect of carbon nanoparticles produced by different methods on the growth of brain tumor and the development of blood vessels. Glioblastoma multiforme cells were cultured on the chorioallantoic membrane of chicken embryo and after 7 days of incubation, were treated with carbon nanoparticles administered in ovo to the tumor. Both types of nanoparticles significantly decreased tumor mass and volume, and vessel area. Quantitative real-time polymerase chain reaction analysis showed downregulated fibroblast growth factor-2 and vascular endothelial growth factor expression at the messenger ribonucleic acid level. The present results demonstrate antiangiogenic activity of carbon nanoparticles, making them potential factors for anticancer therapy.Keywords: cancer, nanoparticle, embryo, angiogenesis, FGF-2, VEGF

  18. Investigating the growth mechanism and optical properties of carbon-coated titanium dioxide nanoparticles

    KAUST Repository

    Anjum, Dalaver H.

    2013-10-01

    TiO2 nanoparticles (NPs) were prepared using flame synthesis and then characterized using transmission electron microscopy. We found that the flame method yields both crystalline TiO2 and amorphous TiO 2 NPs. TEM analysis revealed that only the crystalline TiO 2 NPs were coated with carbon. Based on this observation, we proposed a growth model for the diffusion and precipitation of carbon atoms in TiO 2 NPs. The optical properties of TiO2 NPs were investigated by performing valence electron energy loss spectrometry analysis. We observed that carbon-coated TiO2 NPs have higher absorption in the visible range due to their lower band-gap energy. © 2013 Elsevier B.V.

  19. 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

  20. 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.

  1. Extracellular Synthesis of Silver Nanoparticles by Ralstonia sp. SM8 Isolated from the Sarcheshmeh Copper Mine

    OpenAIRE

    Morahem Ashengroph

    2014-01-01

    Introduction: The biological synthesis of nanoparticles has gained enormous importance due to the development of clean and environmentally-friendly processes. Silver is highly toxic to microbial cells, Nevertheless, it has been reported that several microorganisms are silver resistance and corroborate the microbial reduction of water soluble Ag+ to Ag0 nanoparticles. In this study, native strains of bacteria screen for use as biocatalysts for extracellular synthesis of silver nanoparticles. ...

  2. 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...

  3. 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)

  4. 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)

  5. Laser-driven synthesis and magnetic properties of iron nanoparticles

    International Nuclear Information System (INIS)

    Nanoparticles of iron have been prepared by laser-driven decomposition of iron pentacarbonyl vapor. In this method, an infrared laser rapidly heats a dilute mixture of precursor vapors to decompose the precursor and initiate particle nucleation. It was found that when using SF6 as a photosensitizer during the synthesis, ferrous fluoride (FeF2) was produced as an undesired byproduct in the product powder. The particle size, composition, and crystalline structure have been characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and X-ray photoelectron spectroscopy (XPS). Results of magnetization measurements for small iron nanoparticles (about 5 nm diameter) are also presented, showing superparamagnetic behavior at room temperature, and a blocking temperature near 125 K

  6. Energy Consumption During Nanoparticle Production: How Economic is Dry Synthesis?

    International Nuclear Information System (INIS)

    The production of oxide nanoparticles by selected wet-chemistry or dry processes is compared in terms of energy requirements. Clear differences arise for production using electricity-intensive plasma processes, organic- or chloride-derived flame synthesis and liquid based precipitation processes. In spite of short process chains and elegant reactor design, many dry methods inherently require vastly bigger energy consumption than the multi-step wet processes. Product composition strongly influences the selection of the preferred method of manufacturing in terms of energy requirement: Metal oxide nanoparticles of light elements with high valency, e.g. titania demand high volumes of organic precursors and traditional processes excel in terms of efficiency. Products with heavier elements, more complex composition and preferably lower valency such as doped ceria, zirconia, and most mixed oxide ceramics may be readily manufactured by recently developed dry processes

  7. Nanoparticles of carbon allotropes inhibit glioblastoma multiforme angiogenesis in ovo

    DEFF Research Database (Denmark)

    Grodzik, Marta; Sawosz, Ewa; Wierzbicki, Mateusz; Orlowski, Piotr; Hotowy, Anna Malgorzata; Niemiec, Tomasz; Szmidt, Maciej; Mitura, Katarzyna; Chwalibog, André

    2011-01-01

    The objective of the study was to determine the effect of carbon nanoparticles produced by different methods on the growth of brain tumor and the development of blood vessels. Glioblastoma multiforme cells were cultured on the chrioallantoic membrane of chicken embryo and after 7 days of incubati...

  8. Fluorescent Carbon Nanoparticles in Medicine for Cancer Therapy

    OpenAIRE

    Kumar, Vinit; Toffoli, Giuseppe; Rizzolio, Flavio

    2013-01-01

    Nanotechnology provides exciting opportunities for the development of novel, clinically relevant diagnostic and therapeutic multifunctional systems. Fluorescent carbon nanoparticles (CNPs) due to their intrinsic fluorescence and high biocompatibility are among the best candidates. As innovative nanomaterials, CNPs could be utilized both as nontoxic drug delivery system and bioimaging. We foresee a great future for CNPs in cancer diagnostic and therapy.

  9. Solution plasma synthesis of Si nanoparticles

    Science.gov (United States)

    Saito, Genki; Sakaguchi, Norihito

    2015-06-01

    Silicon nanoparticles (Si-NPs) were directly synthesized from a Si bar electrode via a solution plasma. In order to produce smaller Si-NPs, the effects of different electrolytes and applied voltages on the product were investigated in the experiments detailed in this paper. The results demonstrated that the use of an acidic solution of 0.1 M HCl or HNO3 produced Si-NPs without SiO2 formation. According to the transmission electron microscopy and electron energy-loss spectroscopy, the obtained Si-NPs contained both amorphous and polycrystalline Si particles, among which the smaller Si-NPs tended to be amorphous. When an alkaline solution of K2CO3 was used instead, amorphous SiO2 particles were synthesized owing to the corrosion of Si in the high-temperature environment. The pH values of KCl and KNO3 increased during electrolysis, and the products were partially oxidized in the alkaline solutions. The particle size increased with an increasing applied voltage because the excitation temperature of the plasma increased.

  10. 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.

  11. Synthesis and oxidation of silver nanoparticles

    Science.gov (United States)

    Qi, Hua; Alexson, D. A.; Glembocki, O. J.; Prokes, S. M.

    2011-02-01

    We demonstrated a fast and easy way to synthesize Ag nanoparticles (NPs) on ZnO nanowires (NWs) and silicon substrates by an electroless (EL) plating approach. ZnO NWs used here were grown via vapor-solid (VS) mechanism at 560 °C for 30 min. The stability to oxidation of these EL-produced homogeneous Ag NPs on ZnO nanowires was investigated by surface enhanced Raman spectroscopy (SERS), showing that the attachment of thiol to the Ag surface can slow down the oxidation process, and the SERS signal remains strong for more than ten days. Furthermore, we examined the surface oxidation kinetics of the Ag NPs as a function of NPs size and size distribution by monitoring the oxygen amount in the composites using energy dispersive x-ray (EDX). Results indicate that the EL plated Ag NPs show faster oxidation rates than those produced by e-beam (EB) evaporation in air. We attribute this to the fact that the EL produced silver particles are very small, in the 20 nm range, and thus have high surface energy, thus enhancing the oxidation. These studies provide extensive information related to the Ag NP oxidation rates, which can help in extending the Ag lifetime for various applications.

  12. 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

  13. Peapod-like composite with nickel phosphide nanoparticles encapsulated in carbon fibers as enhanced anode for li-ion batteries.

    Science.gov (United States)

    Zhang, Huijuan; Feng, Yangyang; Zhang, Yan; Fang, Ling; Li, Wenxiang; Liu, Qing; Wu, Kai; Wang, Yu

    2014-07-01

    Herein, we introduce a peapod-like composite with Ni12 P5 nanoparticles encapsulated in carbon fibers as the enhanced anode in Li-ion batteries for the first time. In the synthesis, NiNH4 PO4 ⋅H2 O nanorods act as precursors and sacrificial templates, and glucose molecules serve as the green carbon source. With the aid of hydrogen bonding between the precursor and carbon source, a polymer layer is hydrothermally formed and then rationally converted into carbon fibers upon inert calcination at elevated temperatures. Meanwhile, NiNH4 PO4 ⋅H2 O nanorods simultaneously turn into Ni12 P5 nanoparticles encapsulated in carbon fibers by undergoing a decomposition and reduction process induced by high temperature and the carbon fibers. The obtained composite performs excellently as a Li-ion batteries anode relative to pure-phase materials. Specific capacity can reach 600 m Ah g(-1) over 200 cycles, which is much higher than that of isolated graphitized carbon or phosphides, and reasonably believed to originate from the synergistic effect based on the combination of Ni12 P5 nanoparticles and carbon fibers. Due to the benignity, sustainability, low cost, and abundance of raw materials of the peapod-like composite, numerous potential applications, in fields such as optoelectronics, electronics, specific catalysis, gas sensing, and biotechnology can be envisaged. PMID:24648293

  14. Carbon nanofiber supported bimetallic PdAu nanoparticles for formic acid electrooxidation

    Science.gov (United States)

    Qin, Yuan-Hang; Jiang, Yue; Niu, Dong-Fang; Zhang, Xin-Sheng; Zhou, Xing-Gui; Niu, Li; Yuan, Wei-Kang

    2012-10-01

    Carbon nanofiber (CNF) supported PdAu nanoparticles are synthesized with sodium citrate as the stabilizing agent and sodium borohydride as the reducing agent. High resolution transmission electron microscopy (HRTEM) characterization indicates that the synthesized PdAu particles are well dispersed on the CNF surface and X-ray diffraction (XRD) characterization indicates that the alloying degree of the synthesized PdAu nanoparticles can be improved by adding tetrahydrofuran to the synthesis solution. The results of electrochemical characterization indicate that the addition of Au can promote the electrocatalytic activity of Pd/C catalyst for formic acid oxidation and the CNF supported high-alloying PdAu catalyst possesses better electrocatalytic activity and stability for formic acid oxidation than either the CNF supported low-alloying PdAu catalyst or the CNF supported Pd catalyst.

  15. Nanosecond laser-induced synthesis of nanoparticles with tailorable magneticanisotropy

    International Nuclear Information System (INIS)

    Controlling the magnetic orientation of nanoparticles is important for many applications. Recently, it has been shown that single domain ferromagnetic hemispherical Co nanoparticles prepared by nanosecond laser-induced self-organization, show magnetic orientation that was related to the negative sign of the magnetostrictive coefficient λS [J. Appl. Phys. v103, p073902, 2008]. Here we have extended this work to the Fe50Co50 alloy, which has a positive λS and Ni, which has a negative λS. Patterned arrays of ferromagnetic nanoparticles of Fe50Co50, Ni, (and Co) were synthesized from their ultrathin metal films on SiO2 substrate by nanosecond laser-induced self-organization. The morphology, nanostructure, and magnetic behavior of the nanoparticle arrays were investigated by a combination of electron microscopy, atomic force microscopy, and magnetic force microscopy techniques. Transmission electron microscopy investigations revealed a granular polycrystalline nanostructure, with the number of grains inside the nanoparticle increasing with their diameter. Magnetic force measurements showed that the magnetization direction of the hemispherical Co and Ni nanoparticles was predominantly out-of-plane while those for the Fe50Co50 alloy was in the plane of the substrate. Finite element analysis was used to estimate the average residual strain in the nanoparticles, following laser processing. The difference in behavior is due to the dominating influence of magnetostrictive energy on the magnetization as a result of residual thermal strain following fast laser processing. Since λS is negative for polycrystalline Co and Ni, and positive for Fe50Co50, the tensile residual strain forces the magnetization direction to out-of-plane and in-plane, respectively. This work demonstrates a cost-effective non-epitaxial technique for the synthesis of magnetic nanoparticles with tailored magnetization orientations. - Research Highlights: → Pulsed laser self-organization of

  16. 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

  17. Green synthesis and characterization of se nanoparticles and nanorods

    Science.gov (United States)

    Chen, Huiyu; Yoo, Ji-Beom; Liu, Yaqing; Zhao, Guizhe

    2011-12-01

    Selenium nanoparticles and nanorods were successfully prepared in a mixed solvent of ethylene glycol and water at a relatively low temperature of 85°C. No other surfactant or template was employed, and glucose was used as a green and mild reducing reagent in the current synthesis. The volume ratio of ethylene glycol to water played an important role for controlling the shapes of selenium products. The obtained selenium samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Raman spectra, and UV-vis absorption spectra. The evolution process from amorphous selenium to a trigonal phase complied with a "solid-solution-solid" formation mechanism. HRTEM and SAED results indicate that the trigonal selenium nanorods grow along the [001] direction. This method might provide an environmentally-friendly and low cost route for the synthesis of other related nanomaterials with controlled morphologies.

  18. 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)

  19. Synthesis of Ag@Silica Nanoparticles by Assisted Laser Ablation.

    Science.gov (United States)

    González-Castillo, J R; Rodriguez, E; Jimenez-Villar, E; Rodríguez, D; Salomon-García, I; de Sá, Gilberto F; García-Fernández, T; Almeida, D B; Cesar, C L; Johnes, R; Ibarra, Juana C

    2015-12-01

    This paper reports the synthesis of silver nanoparticles coated with porous silica (Ag@Silica NPs) using an assisted laser ablation method. This method is a chemical synthesis where one of the reagents (the reducer agent) is introduced in nanometer form by laser ablation of a solid target submerged in an aqueous solution. In a first step, a silicon wafer immersed in water solution was laser ablated for several minutes. Subsequently, an AgNO3 aliquot was added to the aqueous solution. The redox reaction between the silver ions and ablation products leads to a colloidal suspension of core-shell Ag@Silica NPs. The influence of the laser pulse energy, laser wavelength, ablation time, and Ag(+) concentration on the size and optical properties of the Ag@Silica NPs was investigated. Furthermore, the colloidal suspensions were studied by UV-VIS-NIR spectroscopy, X-Ray diffraction, and high-resolution transmission electron microscopy (HRTEM). PMID:26464175

  20. 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

  1. 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

  2. Facile synthesis of size controllable dendritic mesoporous silica nanoparticles.

    Science.gov (United States)

    Yu, Ye-Jun; Xing, Jun-Ling; Pang, Jun-Ling; Jiang, Shu-Hua; Lam, Koon-Fung; Yang, Tai-Qun; Xue, Qing-Song; Zhang, Kun; Wu, Peng

    2014-12-24

    The synthesis of highly uniform mesoporous silica nanospheres (MSNs) with dendritic pore channels, particularly ones with particle sizes below 200 nm, is extremely difficult and remains a grand challenge. By a combined synthetic strategy using imidazolium ionic liquids (ILs) with different alkyl lengths as cosurfactants and Pluronic F127 nonionic surfactants as inhibitors of particle growth, the preparation of dendritic MSNs with controlled diameter between 40 and 300 nm was successfully realized. An investigation of dendritic MSNs using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and nitrogen physisorption revealed that the synthesis of dendritic MSNs at larger size (100-300 nm) strongly depends on the alkyl lengths of cationic imidazolium ILs; while the average size of dendritic MSNs can be controlled within the range of 40-100 nm by varying the amount of Pluronic F127. The Au@MSNs can be used as a catalyst for the reduction of 4-nitrophenol by NaBH4 into 4-aminophenol and exhibit excellent catalytic performance. The present discovery of the extended synthesis conditions offers reproducible, facile, and large-scale synthesis of the monodisperse spherical MSNs with precise size control and, thus, has vast prospects for future applications of ultrafine mesostructured nanoparticle materials in catalysis and biomedicine. PMID:25454255

  3. Porous Carbon-Supported Gold Nanoparticles for Oxygen Reduction Reaction: Effects of Nanoparticle Size.

    Science.gov (United States)

    Wang, Likai; Tang, Zhenghua; Yan, Wei; Yang, Hongyu; Wang, Qiannan; Chen, Shaowei

    2016-08-17

    Porous carbon-supported gold nanoparticles of varied sizes were prepared using thiolate-capped molecular Au25, Au38, and Au144 nanoclusters as precursors. The organic capping ligands were removed by pyrolysis at controlled temperatures, resulting in good dispersion of gold nanoparticles within the porous carbons, although the nanoparticle sizes were somewhat larger than those of the respective nanocluster precursors. The resulting nanocomposites displayed apparent activity in the electroreduction of oxygen in alkaline solutions, which increased with decreasing nanoparticle dimensions. Among the series of samples tested, the nanocomposite prepared with Au25 nanoclusters displayed the best activity, as manifested by the positive onset potential at +0.95 V vs RHE, remarkable sustainable stability, and high numbers of electron transfer at (3.60-3.92) at potentials from +0.50 to +0.80 V. The performance is comparable to that of commercial 20 wt % Pt/C. The results demonstrated the unique feasibility of porous carbon-supported gold nanoparticles as high-efficiency ORR catalysts. PMID:27454707

  4. 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...

  5. Hydrothermal Synthesis of Ultrasmall Pt Nanoparticles as Highly Active Electrocatalysts for Methanol Oxidation

    OpenAIRE

    Wenhai Ji; Weihong Qi; Shasha Tang; Hongcheng Peng; Siqi Li

    2015-01-01

    Ultrasmall nanoparticles, with sizes in the 1–3 nm range, exhibit unique properties distinct from those of free molecules and larger-sized nanoparticles. Demonstrating that the hydrothermal method can serve as a facile method for the synthesis of platinum nanoparticles, we successfully synthesized ultrasmall Pt nanoparticles with an average size of 2.45 nm, with the aid of poly(vinyl pyrrolidone) (PVP) as reducing agents and capping agents. Because of the size effect, these ultrasmall Pt nano...

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

    OpenAIRE

    A Geetha; Sakthivel, R.; J. Mallika; R. Kannusamy; Rajendran, R.

    2016-01-01

    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 crystall...

  7. Modified carbon nanoparticle-chitosan film electrodes: Physisorption versus chemisorption

    Energy Technology Data Exchange (ETDEWEB)

    Rassaei, Liza; Sillanpaeae, Mika [Laboratory of Applied Environmental Chemistry, Department of Environmental Sciences, University of Kuopio, Patteristonkatu 1, 50101 Mikkeli (Finland); Marken, Frank [Department of Chemistry, University of Bath, Bath BA2 7AY (United Kingdom)

    2008-08-01

    Surface functionalised carbon nanoparticles of ca. 8 nm diameter co-assemble with chitosan into stable thin film electrodes at glassy carbon surfaces. Robust electrodes for application in sensing or electrocatalysis are obtained in a simple solvent evaporation process. The ratio of chitosan binder backbone to carbon nanoparticle conductor determines the properties of the resulting films. Chitosan (a poly-D-glucosamine) has a dual effect (i) as the binder for the mesoporous carbon composite structure and (ii) as binding site for redox active probes. Physisorption due to the positively charged ammonium group (pK{sub A} {approx} 6.5) occurs, for example, with anionic indigo carmine (a reversible 2e{sup -}-2H{sup +} reduction system in aqueous media). Chemisorption at the amine functionalities is demonstrated with 2-bromo-methyl-anthraquinone in acetonitrile (resulting in a reversible 2e{sup -}-2H{sup +} anthraquinone reduction system in aqueous media). Redox processes within the carbon nanoparticle-chitosan films are studied and at sufficiently high scan rates diffusion of protons (buffer concentration depended) is shown to be rate limiting. The chemisorption process provides a much more stable interfacial redox system with a characteristic and stable pH response over a pH 2-12 range. Chemisorption and physisorption can be employed simultaneously in a complementary binding process. (author)

  8. Photothermal Effects and Applications of Polydimethylsiloxane Membranes with Carbon Nanoparticles

    Directory of Open Access Journals (Sweden)

    Reinher Pimentel-Domínguez

    2016-03-01

    Full Text Available The advent of nanotechnology has triggered novel developments and applications for polymer-based membranes with embedded or coated nanoparticles. As an example, interaction of laser radiation with metallic and carbon nanoparticles has shown to provide optically triggered responses in otherwise transparent media. Incorporation of these materials inside polymers has led to generation of plasmonic and photothermal effects through the enhanced optical absorption of these polymer composites. In this work, we focus on the photothermal effects produced in polydimethylsiloxane (PDMS membranes with embedded carbon nanoparticles via light absorption. Relevant physical parameters of these composites, such as nanoparticle concentration, density, geometry and dimensions, are used to analyze the photothermal features of the membranes. In particular, we analyze the heat generation and conduction in the membranes, showing that different effects can be achieved and controlled depending on the physical and thermal properties of the composite material. Several novel applications of these light responsive membranes are also demonstrated, including low-power laser-assisted micro-patterning and optomechanical deformation. Furthermore, we show that these polymer-nanoparticle composites can also be used as coatings in photonic and microfluidic applications, thereby offering an attractive platform for developing light-activated photonic and optofluidic devices.

  9. 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.

  10. Effect of solvent on the synthesis of SnO2 nanoparticles

    Science.gov (United States)

    Kumar, Virender; Singh, Kulwinder; Singh, Karamjit; Kumari, Sudesh; Kumar, Akshay; Thakur, Anup

    2016-05-01

    Tin oxide (SnO2) nanoparticles have been synthesized by co-precipitation method. The synthesized nanoparticles have been characterized by X-ray diffraction (XRD) and Ultraviolet-Visible spectroscopy (UV-VIS). XRD analysis confirmed the formation of single phase of SnO2 nanoparticles. It has been found that solvents played important role in controlling the crystallite size of SnO2 nanoparticles. The XRD analysis showed well crystallized tetragonal SnO2 nanoparticles. The crystallite size of SnO2 nanoparticles varies with the solvent. Tauc plot showed that optical band gap was also tailored by controlling the solvent during synthesis.

  11. 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

  12. Facile-green synthesis of nitrogen-doped carbon-supported ultrafine silver catalyst with enhanced electrocatalytic property

    International Nuclear Information System (INIS)

    Highlights: • Ultrafine Ag nanoparticles were grown on carbon surfaces with no toxic reagent. • The reduction temperature of silver nanoparticles was at room temperature. • The sample showed a superior oxygen reduction reaction activity. • A feasible synthesis mechanism has been proposed. -- Abstract: We have demonstrated a facile and green strategy to synthesize ultrafine silver nanoparticles monodispersed on N-doped three-dimensional carbon nanocloud surfaces without any toxic reagent. Folic acid was employed as the carbon precursor for forming N-doped carbon nanoflakes by a hydrothermal method. The as-prepared products can serve as both reducing agent and substrate, on which a high density of ultrafine Ag nanocrystals is stably grown in a homogeneously dispersive state spontaneously at room temperature. A feasible synthesis mechanism has been proposed by characterization of carbon precursor, nanomaterials composited without and with silver nanoparticles. It was found that the ethylenic and oxygenated groups led to the reduction process. The nanohybrids showed an enhanced electrocatalytic activity toward oxygen reduction reaction (ORR) in alkaline solution via a four-electron pathway. The catalyst also exhibited strong duration of methanol and good stability compared to commercial Pt/C catalysts

  13. Apparatus for producing carbon-coated nanoparticles and carbon nanospheres

    Science.gov (United States)

    Perry, W. Lee; Weigle, John C.; Phillips, Jonathan

    2015-10-20

    An apparatus for producing carbon-coated nano- or micron-scale particles comprising a container for entraining particles in an aerosol gas, providing an inlet for carbon-containing gas, providing an inlet for plasma gas, a proximate torch for mixing the aerosol gas, the carbon-containing gas, and the plasma gas, bombarding the mixed gases with microwaves, and providing a collection device for gathering the resulting carbon-coated nano- or micron-scale particles. Also disclosed is a method and apparatus for making hollow carbon nano- or micro-scale spheres.

  14. 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.

  15. Fluorescent carbon nanoparticles: A low-temperature trypsin-assisted preparation and Fe(3+) sensing.

    Science.gov (United States)

    Feng, Jie; Chen, Yonglei; Han, Yangxia; Liu, Juanjuan; Ren, Cuiling; Chen, Xingguo

    2016-07-01

    In recent years, extensive researches are focused on the fluorescent carbon nanoparticles (CNPs) due to their excellent photochemical, biocompatible and water-soluble properties. However, these synthesis methods are generally suffered from tedious processes. In this paper, fluorescent carbon nanoparticles are synthesized by a facile, one-pot, low-temperature method with trypsin and dopamine as precursors. The synthesis process avoids any heating operation and organic solvent, which provides a "green" and effective preparation route. The obtained CNPs exhibit excellent water-solubility, salt-tolerance and photostability. Based on the synergistic action of the inner filter effect and static quenching mechanism, the CNPs are exploited as a "turn-off" fluorescence sensor for sensitive and selective detection of Fe(3+) ions. The probe shows a wide linear range from 0.1 to 500 μM, with a limit of detection of 30 nM. Furthermore, the as-fabricated fluorescent sensing system is successfully applied to the analysis of Fe(3+) in biological samples such as human urine and serum samples with satisfactory recoveries (92.8-113.3%). PMID:27216399

  16. Ostwald Ripening of Platinum Nanoparticles Confined in a Carbon Nanotube/Silica-Templated Cylindrical Space

    Directory of Open Access Journals (Sweden)

    Cintia Mateo-Mateo

    2012-01-01

    Full Text Available Sintering of nanoparticles mediated by an Ostwald ripening mechanism is generally assessed examining the final particle size distributions. Based on this methodology, a general approach for depositing platinum nanoparticles onto carbon nanotubes in solution has been employed in order to evaluate the sintering process of these metallic nanoparticles at increasing temperatures in a carbon nanotube/silica-templated confined space.

  17. Ostwald Ripening of Platinum Nanoparticles Confined in a Carbon Nanotube/Silica-Templated Cylindrical Space

    OpenAIRE

    Cintia Mateo-Mateo; Carmen Vázquez-Vázquez; Moisés Pérez-Lorenzo; Verónica Salgueiriño; Correa-Duarte, Miguel A.

    2012-01-01

    Sintering of nanoparticles mediated by an Ostwald ripening mechanism is generally assessed examining the final particle size distributions. Based on this methodology, a general approach for depositing platinum nanoparticles onto carbon nanotubes in solution has been employed in order to evaluate the sintering process of these metallic nanoparticles at increasing temperatures in a carbon nanotube/silica-templated confined space.

  18. Synthesis of carbon-13-labeled tetradecanoic acids.

    Science.gov (United States)

    Sparrow, J T; Patel, K M; Morrisett, J D

    1983-07-01

    The synthesis of tetradecanoic acid enriched with 13C at carbons 1, 3, or 6 is described. The label at the carbonyl carbon was introduced by treating 1-bromotridecane with K13CN (90% enriched) to form the 13C-labeled nitrile, which upon hydrolysis yielded the desired acid. The [3-13C]tetradecanoic acid was synthesized by alkylation of diethyl sodio-malonate with [1-13C]1-bromododecane; the acid was obtained upon saponification and decarboxylation. The label at the 6 position was introduced by coupling the appropriately labeled alkylcadmium chloride with the half acid chloride methyl ester of the appropriate dioic acid, giving the corresponding oxo fatty acid ester. Formation of the tosylhydrazone of the oxo-ester followed by reduction with sodium cyanoborohydride gave the labeled methyl tetradecanoate which, upon hydrolysis, yielded the desired tetradecanoic acid. All tetradecanoic acids were identical to unlabeled analogs as evaluated by gas-liquid chromatography and infrared or NMR spectroscopy. These labeled fatty acids were used subsequently to prepare the correspondingly labeled diacyl phosphatidylcholines. PMID:6631228

  19. Rapid synthesis of Co, Ni co-doped ZnO nanoparticles: Optical and electrochemical properties

    International Nuclear Information System (INIS)

    We report for the first time a rapid preparation of Zn1−2xCoxNixO nanoparticles via a versatile and environmentally friendly route, microwave-assisted hydrothermal (MAH) method. The Co, Ni co-doped ZnO nanoparticles present an effect on photoluminescence and electrochemical properties, exhibiting excellent electrocatalytic performance compared to undoped ZnO sample. Photoluminescence spectroscopy measurements indicated the reduction of the green–orange–red visible emission region after adding Co and Ni ions, revealing the formation of alternative pathways for the generated recombination. The presence of these metallic ions into ZnO creates different defects, contributing to a local structural disorder, as revealed by Raman spectra. Electrochemical experiments revealed that the electrocatalytic oxidation of dopamine on ZnO attached to multi-walled carbon nanotubes improved significantly in the Co, Ni co-doped ZnO samples when compared to pure ZnO. - Graphical abstract: Rapid synthesis of Co, Ni co-doped ZnO nanoparticles: optical and electrochemical properties. Co, Ni co-doped ZnO hexagonal nanoparticles with optical and electrocatalytic properties were successfully prepared for the first time using a microwave hydrothermal method at mild conditions. - Highlights: • Co2+ and Ni2+ into ZnO lattice obtained a mild and environmentally friendly process. • The heating method strongly influences in the growth and shape of the particles. • Short-range defects generated by the ions insertion affects the photoluminescence. • Doped ZnO nanoparticles improve the electrocatalytic properties of pure oxide

  20. Rapid synthesis of Co, Ni co-doped ZnO nanoparticles: Optical and electrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Romeiro, Fernanda C.; Marinho, Juliane Z.; Lemos, Samantha C.S. [Instituto de Química, Universidade Federal de Uberlândia, 38400-902 Uberlândia, MG (Brazil); Moura, Ana P. de [LIEC, Instituto de Química, Universidade Estadual Paulista, 14800-900 Araraquara, SP (Brazil); Freire, Poliana G. [Instituto de Química, Universidade Federal de Uberlândia, 38400-902 Uberlândia, MG (Brazil); Silva, Luis F. da; Longo, Elson [LIEC, Instituto de Química, Universidade Estadual Paulista, 14800-900 Araraquara, SP (Brazil); Munoz, Rodrigo A.A. [Instituto de Química, Universidade Federal de Uberlândia, 38400-902 Uberlândia, MG (Brazil); Lima, Renata C., E-mail: rclima@iqufu.ufu.br [Instituto de Química, Universidade Federal de Uberlândia, 38400-902 Uberlândia, MG (Brazil)

    2015-10-15

    We report for the first time a rapid preparation of Zn{sub 1−2x}Co{sub x}Ni{sub x}O nanoparticles via a versatile and environmentally friendly route, microwave-assisted hydrothermal (MAH) method. The Co, Ni co-doped ZnO nanoparticles present an effect on photoluminescence and electrochemical properties, exhibiting excellent electrocatalytic performance compared to undoped ZnO sample. Photoluminescence spectroscopy measurements indicated the reduction of the green–orange–red visible emission region after adding Co and Ni ions, revealing the formation of alternative pathways for the generated recombination. The presence of these metallic ions into ZnO creates different defects, contributing to a local structural disorder, as revealed by Raman spectra. Electrochemical experiments revealed that the electrocatalytic oxidation of dopamine on ZnO attached to multi-walled carbon nanotubes improved significantly in the Co, Ni co-doped ZnO samples when compared to pure ZnO. - Graphical abstract: Rapid synthesis of Co, Ni co-doped ZnO nanoparticles: optical and electrochemical properties. Co, Ni co-doped ZnO hexagonal nanoparticles with optical and electrocatalytic properties were successfully prepared for the first time using a microwave hydrothermal method at mild conditions. - Highlights: • Co{sup 2+} and Ni{sup 2+} into ZnO lattice obtained a mild and environmentally friendly process. • The heating method strongly influences in the growth and shape of the particles. • Short-range defects generated by the ions insertion affects the photoluminescence. • Doped ZnO nanoparticles improve the electrocatalytic properties of pure oxide.

  1. 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.

  2. 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.

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

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • La2(WO4)3 as one of semiconducting materials. • H.V. electrospinning was used to synthesize La2(WO4)3 interconnecting nanoparticles. • A promising material for photoemission. - Abstract: Lanthanum tungstate (La2(WO4)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 La2(WO4)3 fibers with 200–700 nm in diameter, two main Raman peaks at 945 and 927 cm−1, FTIR stretching modes at 936 and 847 cm−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

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

    International Nuclear Information System (INIS)

    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

  5. 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.

  6. 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.

  7. 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.

  8. N-heterocyclic carbene catalyzed synthesis of dimethyl carbonate via transesterification of ethylene carbonate with methanol

    OpenAIRE

    Guang-Fen Du; Hao Guo; Ying Wang; Wen-Juan Li; Wei-Jie Shi; Bin Dai

    2015-01-01

    An organocatalytic protocol for the synthesis of dimethyl carbonate has been developed. Under the catalysis of 5 mol% N-heterocyclic carbenes, ethylene carbonate undergoes transesterification reaction with methanol under very mild reaction conditions, producing dimethyl carbonate with high efficiency. Furthermore, this N-heterocyclic carbene promoted transesterification can be scaled-up easily without lose of the conversion of dimethyl carbonate.

  9. 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.

  10. Synthesis of Tungsten Diselenide Nanoparticles by Chemical Vapor Condensation Method

    Directory of Open Access Journals (Sweden)

    Oleg V. Tolochko

    2015-09-01

    Full Text Available Crystalline tungsten diselenide (WSe2 nanoparticles have been synthesized by a gas phase reaction using tungsten hexacarbonyl and elemental selenium as precursors. The WSe2 nanoparticle morphology varies from the spherical shape to flake-like layered structures. Mean size in smaller dimension are less than 5 nm and the number of layers decreased linearly with decreasing of reaction time and concentration of carbonyl in the gas phase. The mean value of interlayer distance in <0001> direction is comparable with the microscopic values. The selenium-to-tungsten atomic ratios of 2.07, 2.19 and 2.19 were determined respectively, approach to the stoichiometric ratio of 2:1. Main impurities are oxygen and carbon and strongly interrelated with carbonyl concentration in the gas phase.DOI: http://dx.doi.org/10.5755/j01.ms.21.3.7356

  11. Evaluation of the tracing effect of carbon nanoparticle and carbon nanoparticle-epirubicin suspension in axillary lymph node dissection for breast cancer treatment

    OpenAIRE

    Du, Junze; Zhang, Yongsong; Ming, Jia; Liu, Jing; Zhong, Ling; Liang, Quankun; Fan, Linjun; Jiang, Jun

    2016-01-01

    Abstracts Background Carbon nanoparticle suspension, using smooth carbon particles at a diameter of 21 nm added with suspending agents, is a stable suspension of carbon pellets of 150 nm in diameter. It is obviously inclined to the lymphatic system. There were some studies reporting that carbon nanoparticles are considered as superior tracers for sentinel lymph nodes because of their stability and operational feasibility. However, there were few study concerns about the potential treatment ef...

  12. Mechanism of Synthesis of Ultra-Long Single Wall Carbon Nanotubes in Arc Discharge Plasma

    Energy Technology Data Exchange (ETDEWEB)

    Keidar, Michael [George Washington University

    2013-06-23

    In this project fundamental issues related to synthesis of single wall carbon nanotubes (SWNTs), which is relationship between plasma parameters and SWNT characteristics were investigated. Given that among plasma-based techniques arc discharge stands out as very advantageous in several ways (fewer defects, high flexibility, longer lifetime) this techniques warrants attention from the plasma physics and plasma technology standpoint. Both experimental and theoretical investigations of the plasma and SWNTs synthesis were conducted. Experimental efforts focused on plasma diagnostics, measurements of nanostructures parameters, and nanoparticle characterization. Theoretical efforts focused to focus on multi-dimensional modeling of the arc discharge and single wall nanotube synthesis in arc plasmas. It was demonstrated in experiment and theoretically that controlling plasma parameters can affect nanostucture synthesis altering SWNT properties (length and diameter) and leading to synthesis of new structures such as a few-layer graphene. Among clearly identified parameters affecting synthesis are magnetic and electric fields. Knowledge of the plasma parameters and discharge characteristics is crucial for ability to control synthesis process by virtue of both magnetic and electric fields. New graduate course on plasma engineering was introduced into curriculum. 3 undergraduate students were attracted to the project and 3 graduate students (two are female) were involved in the project. Undergraduate student from Historically Black University was attracted and participated in the project during Summer 2010.

  13. Advances in Pd Nanoparticle Size Decoration of Mesoporous Carbon Spheres for Energy Application

    Science.gov (United States)

    Zielinska, Beata; Michalkiewicz, Beata; Mijowska, Ewa; Kalenczuk, Ryszard Józef

    2015-10-01

    Pd nanoparticles with different sizes and diameter distributions were successfully deposited on the surface of disordered mesoporous carbon spheres (DMHCS). The size and diameter distribution of the Pd particles were controlled by the application of different experimental conditions. Two methods of synthesis (reflux and impregnation) and two Pd precursors (palladium (II) acetyloacetonate (Pd (acac ) 2) and palladium (II) acetate (Pd(OAc)2)) were investigated and compared for the preparation of Pd-decorated DMHCS. The hydrogen storage properties of the pristine DMHCS and Pd-modified DMHCS at 40 °C and a pressure range of 0-45 bar were studied. The results showed that Pd-supported carbon samples synthesized in the presence of Pd(OAc)2 exhibited enhanced hydrogen storage capacity in respect to the pristine DMHCS. The maximum hydrogen storage of 0.38 wt.% exhibited the sample with the Pd nanoparticle diameter distribution of 2-14 nm and the average Pd crystallite size of 7.6 nm. It was found that the Pd nanoparticle content, size, and diameter distribution have a noticeable influence on H2 storage capacity.

  14. A Two-Step Hydrothermal Synthesis Approach to Monodispersed Colloidal Carbon Spheres

    Directory of Open Access Journals (Sweden)

    Yu Aibing

    2009-01-01

    Full Text Available Abstract This work reports a newly developed two-step hydrothermal method for the synthesis of monodispersed colloidal carbon spheres (CCS under mild conditions. Using this approach, monodispersed CCS with diameters ranging from 160 to 400 nm were synthesized with a standard deviation around 8%. The monomer concentration ranging from 0.1 to 0.4 M is in favor of generation of narrower size distribution of CCS. The particle characteristics (e.g., shape, size, and distribution and chemical stability were then characterized by using various techniques, including scanning electron microscopy (SEM, FT-IR spectrum analysis, and thermalgravity analysis (TGA. The possible nucleation and growth mechanism of colloidal carbon spheres were also discussed. The findings would be useful for the synthesis of more monodispersed nanoparticles and for the functional assembly.

  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. Chemical Synthesis of Metal Nanoparticles in Aqueous Solutions with the Presence of Some Additives

    International Nuclear Information System (INIS)

    Metal nanoparticles having interesting shapes can be prepared in aqueous solutions through simple reductions of metal ions with the presence of some additive reagents, such as cetyltrimethylammonium bromide and hexamethylenetetramine. In this review, some successful results for shape-controlled synthesis of metal nanoparticles in our group are summarized, which includes the synthesis of palladium nano cubes, palladium nano bricks, gold nano tripods. In addition, combining with indium tin oxide electrode surfaces, shape-controlled growth is shown to be possible to form gold nano plates and copper oxide nano wires. Even in relatively mild synthetic conditions, interesting shape-controlled synthesis of metal nanoparticles is possible. (author)

  17. 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.

  18. 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.

  19. Nickel Nanoparticles for Enhancing Carbon Capture

    OpenAIRE

    Gaurav Ashok Bhaduri; Mohammed A. H. Alamiry; Lidija Šiller

    2015-01-01

    Hydration reaction of CO2 is one of the rate limiting steps for CO2 absorption (in aqueous solutions) and aqueous CO2 mineralization. The catalytic activity of nickel nanoparticles (NiNPs) for CO2 hydration is studied at different temperatures, pH, and low CO2 partial pressures to mimic the true flue gas conditions. Results show that NiNPs can work as active catalyst for hydration of CO2 in applications such as CO2 separation and CO2 mineralization. The NiNPs display optimum activity within 2...

  20. 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.

  1. A facile hydrothermal approach for construction of carbon coating on TiO2 nanoparticles

    Science.gov (United States)

    Olurode, Kehinde; Neelgund, Gururaj M.; Oki, Aderemi; Luo, Zhiping

    2012-04-01

    Herein a facile hydrothermal approach is used to construct carbon coated TiO2 nanoparticles employing dextrose as the source of carbon. The procedure is operated at a low temperature of 200 °C. Fourier infrared spectroscopy demonstrated the successful coating of carbon on TiO2 nanoparticles. The phase composition of TiO2 and carbon coated TiO2 nanoparticles were studied using X-ray diffraction and the surface morphology was analyzed by scanning and transmission electron microscopy. The existence of carbon coating on TiO2 nanoparticles was revealed by thermogravimetric analysis through different thermograms exhibited for TiO2 and carbon coated TiO2 nanoparticles. The reported method offers a simple and efficient approach for production of carbon coated TiO2 nanoparticles.

  2. Green synthesis of nanoparticles and its potential application.

    Science.gov (United States)

    Hussain, Imtiyaz; Singh, N B; Singh, Ajey; Singh, Himani; Singh, S C

    2016-04-01

    Nanotechnology is a new and emerging technology with wealth of applications. It involves the synthesis and application of materials having one of the dimensions in the range of 1-100 nm. A wide variety of physico-chemical approaches are being used these days for the synthesis of nanoparticles (NPs). However, biogenic reduction of metal precursors to produce corresponding NPs is eco-friendly, less expensive, free of chemical contaminants for medical and biological applications where purity of NPs is of major concern. Biogenic reduction is a "Bottom Up" approach similar to chemical reduction where a reducing agent is replaced by extract of a natural products with inherent stabilizing, growth terminating and capping properties. Furthermore, the nature of biological entities in different concentrations in combination with reducing organic agents influence the size and shape of NPs. Present review focuses on microbes or plants based green synthesis of Ag, Au, Cu, Fe, Pd, Ru, PbS, CdS, CuO, CeO2, Fe3O4, TiO2, and ZnO NPs and their potential applications. PMID:26721237

  3. Chemoselective Synthesis of Carbamates using CO2 as Carbon Source.

    Science.gov (United States)

    Riemer, Daniel; Hirapara, Pradipbhai; Das, Shoubhik

    2016-08-01

    Synthesis of carbamates directly from amines using CO2 as the carbon source is a straightforward and sustainable approach. Herein, we describe a highly effective and chemoselective methodology for the synthesis of carbamates at room temperature and atmospheric pressure. This methodology can also be applied to protect the amino group in amino acids and peptides, and also to synthesize important pharmaceuticals. PMID:27376902

  4. Towards Green Cyclic Carbonate Synthesis : Heterogeneous and Homogeneous Catalyst Development

    OpenAIRE

    Stewart, J A

    2015-01-01

    This PhD research serves to implement both known and novel catalytic systems for the purpose of cyclic carbonate synthesis from biomass-derived substrates. Such products have been earmarked as potential monomers for non-isocyanate polyurethanes (NIPUs), amongst other uses. Particular attention has been placed on operating under the guidance of the 12 principles of Green Chemistry as posited by Anastas et al. Following an in depth literature discussion of catalytic cyclic carbonate synthesis i...

  5. Carbonation acceleration of calcium hydroxide nanoparticles: induced by yeast fermentation

    Science.gov (United States)

    Lopez-Arce, Paula; Zornoza-Indart, Ainara

    2015-09-01

    Carbonation of Ca(OH)2 nanoparticles and consolidation of limestone are accelerated by high humidity and a yeast fermentation system that supplies a saturated atmosphere on CO2, H2O vapor and ethanol during 28 days. Nanoparticles were analyzed by X-ray diffraction and differential thermal analyses with thermogravimetry. Spectrophotometry, scanning electron microscopy analyses, and hydric and mechanical tests were also performed in stones specimens. Samples exposed to the yeast environment achieve 100 % relative CaCO3 yield, whereas at high humidity but without the yeast and under laboratory environment, relative yields of 95 % CaCO3 and 15 % CaCO3 are, respectively, reached, with white crusts and glazing left on the stone surfaces when the nanoparticles are applied at a concentration of 25 g/l. The largest increase in the drilling resistance and surface hardness values with slight increase in the capillarity absorption and desorption coefficients and with lesser stone color changes are produced at a concentration of 5 g/l, in the yeast system environment. This especially happens in stone specimens initially with bimodal pore size distributions, more amounts of pores with diameters between 0.1 and 1 µm, higher open porosity values and faster capillary coefficients. An inexpensive and reliable method based on water and yeast-sugar solution is presented to speed up carbonation of Ca(OH)2 nanoparticles used as a consolidating product to improve the mechanical properties of decayed limestone from archaeological and architectural heritage.

  6. DSC Study on Polypropylene Modified with Calcium Carbonate Nanoparticles

    International Nuclear Information System (INIS)

    The exposure of polypropylene containing various concentrations of calcium carbonate nanoparticles was performed in air and water. The radiolysis products of water determine different behaviour of polymer substrate. The irradiation effect induced on polymer and the contribution of nanoparticles to the scavenging of oxygenated products that were created during γ exposure were investigated by DSC measurements over the temperature range from 340-400 K, the usual temperatures for thermal overcharge. Two kinds of carbonate particles, one type is represented by unmodified filler, while the second type is the superficially modified with stearic acid. The covering of particle surface with stearic acid confers to them a different ability in the abstraction of degradation products formed in irradiated isotactic polypropylene

  7. Carbon Nanoparticles in Nematic Liquid Crystals

    Institute of Scientific and Technical Information of China (English)

    S.Eren San; Mustafa Okutan; O(g)uz K(o)ysal; Yusuf Yer-li

    2008-01-01

    Fullerene G60,C70,single-walled and multi-walled carbon nanotubes and graphene sheets are doped to nematic liquid crystal(LC)host in the same percentage.Planar samples of these mixtures are prepared and our measurements constitute an optimization basis for possible applications.Fullerene balls are found to be the best compatible material for optical aims and reorientation of LC molecules,while the carbon nanotubes experience some reorientation possibility in LC media and graphene layers are good barriers to preserve reorientation.

  8. Influence of ferrite stabilizing elements and Co on structure and magnetic properties of carbon-encapsulated iron nanoparticles synthesized in thermal plasma jet

    International Nuclear Information System (INIS)

    Highlights: • Inclusion of ferrite stabilizing elements reduces the diameter of CEINs. • Inclusion of ferrite stabilizing elements increases the amount of austenite. • Inclusion of Al, Ti, Cr and V causes formation of few layer graphene. • Magnetic performance of CEINs can be largely improved by post annealing. - Abstract: The encapsulation of Fe nanoparticles in protective carbon coatings always leads to formation of undesired paramagnetic austenite phase. Various ferrite stabilizing elements were included in the synthesis process to verify whether their inclusion may minimize the austenite content in carbon-encapsulated iron nanoparticles synthesized in thermal plasma jet. Eight ferrite stabilizing elements (Si, Al, Mo, Ti, Zr, Cr, W and V) and one austenite promoting additive (Co) were tested. Their influence on the synthesis yield, phase composition, morphology and magnetic properties of carbon-encapsulated iron nanoparticles was studied. It was found that the addition of ferrite stabilizers strongly influences the diameter distribution, graphitization degree, phase composition and magnetic properties. Contrary to the thermodynamic predictions the inclusion of ferrite stabilizing elements caused a substantial worsening of magnetic performance in carbon-encapsulated iron nanoparticles. It has been also shown that the subsequent heat treatment of carbon-encapsulated iron nanoparticles significantly improves their magnetic properties

  9. Presence of Amorphous Carbon Nanoparticles in Food Caramels

    OpenAIRE

    Md Palashuddin Sk; Amit Jaiswal; Anumita Paul; Siddhartha Sankar Ghosh; Arun Chattopadhyay

    2012-01-01

    We report the finding of the presence of carbon nanoparticles (CNPs) in different carbohydrate based food caramels, viz. bread, jaggery, sugar caramel, corn flakes and biscuits, where the preparation involves heating of the starting material. The CNPs were amorphous in nature; the particles were spherical having sizes in the range of 4–30 nm, depending upon the source of extraction. The results also indicated that particles formed at higher temperature were smaller than those formed at lower ...

  10. Electrochemical Properties of Carbon Nanoparticles Entrapped in Silica Matrix

    OpenAIRE

    Bok, Sangho; Lubguban, Arnold A.; Gao, Yuanfang; Bhattacharya, Shantanu; Korampally, Venu; Hossain, Maruf; Gillis, Kevin D.; Gangopadhyay, Shubhra

    2008-01-01

    Carbon-based electrode materials have been widely used for many years for electrochemical charge storage, energy generation, and catalysis. We have developed an electrode material with high specific capacitance by entrapping graphite nanoparticles into a sol-gel network. Films from the resulting colloidal suspensions were highly porous due to the removal of the entrapped organic solvents from sol-gel matrix giving rise to high Brunauer-Emmett-Teller (BET) specific surface areas (654 m2/g) and...

  11. Redeposition of electrochemically dissolved platinum as nanoparticles on carbon

    DEFF Research Database (Denmark)

    Norgaard, C. F.; Stamatin, S. N.; Skou, E. M.

    2014-01-01

    Electrochemical dissolution of platinum has been proposed by several research groups as an environmentally friendly way to recover platinum from catalytic structures such as fuel cell electrodes. For the case of electrochemical dissolution of platinum in hydrochloric acid electrolyte, the present...... communication reports a simple chemical method for reprecipitating platinum as nanoparticles of reasonable particle size on a carbon substrate without intermediary separation and handling of solid platinum salt. After electrochemical dissolution, platinum was reprecipitated using a polyol based method. Platinum...

  12. Laser-generated plasma by carbon nanoparticles embedded into polyethylene

    Czech Academy of Sciences Publication Activity Database

    Torrisi, L.; Ceccio, G.; Cutroneo, Mariapompea

    2016-01-01

    Roč. 375, MAY (2016), s. 93-99. ISSN 0168-583X R&D Projects: GA ČR(CZ) GBP108/12/G108; GA MŠk(CZ) LM2011019 Institutional support: RVO:61389005 Keywords : carbon nanoparticles * laser -generated plasma * Time-of-flight measurements * advanced targets Subject RIV: BG - Nuclear, Atomic and Molecular Physics , Colliders Impact factor: 1.124, year: 2014

  13. Antimony nanoparticles anchored in three-dimensional carbon network as promising sodium-ion battery anode

    Science.gov (United States)

    Luo, Wen; Zhang, Pengfei; Wang, Xuanpeng; Li, Qidong; Dong, Yifan; Hua, Jingchen; Zhou, Liang; Mai, Liqiang

    2016-02-01

    A novel composite with antimony (Sb) nanoparticles anchored in three-dimensional carbon network (denoted as SbNPs@3D-C) is successfully synthesized via a NaCl template-assisted self-assembly strategy, followed by freeze-drying and one-step in-situ carbonization. The three-dimensional interconnected macroporous carbon framework can not only stabilize the architecture and buffer the volume expansion for Sb nanoparticles, but also provide high electrical conductivity for the whole electrode. Consequently, as a sodium-ion battery anode, the SbNPs@3D-C delivers a high reversible capacity (456 mAh g-1 at 100 mA g-1), stable cycling performance (94.3% capacity retention after 500 cycles at 100 mA g-1) as well as superior rate capability (270 mAh g-1 at 2000 mA g-1). When compared with commercial Sb particles, the SbNPs@3D-C exhibits dramatically enhanced electrochemical performance. Free from expensive template sources and complex manipulation, this work might shed some light on the synthesis of low-cost and high-performance materials for the next "beyond lithium" battery generation.

  14. Unique Sandwiched Carbon Sheets@Ni-Mn Nanoparticles for Enhanced Oxygen Evolution Reaction.

    Science.gov (United States)

    Zhang, Yan; Zhang, Huijuan; Yang, Jiao; Bai, Yuanjuan; Qiu, Huajun; Wang, Yu

    2016-05-11

    A unique sandwich-like architecture, where Ni-Mn nanoparticles are enveloped in coupled carbon sheets (CS@Ni-Mn), has been successfully fabricated. In the synthesis process, a great quantity of uniform NiMnO3 nanosheets generated by a universal hydrothermal method acts as precursors and templates and the cheap, environmentally friendly and recyclable glucose functions as a green carbon source. Via subsequent hydrothermal reaction and thermal annealing, sandwiched nanocomposites with Ni-Mn nanoparticles embedded inside and carbon sheets encapsulating outside can be massively prepared. The novel sandwich-like CS@Ni-Mn possesses numerous advantages, such as an intrinsic porous feature, large specific surface area, and enhanced electronic conductivity. Moreover, as a promising NiMn-based oxygen evolution reaction (OER) catalyst, the special sandwiched nanostructure demonstrates improved electrochemical properties in 1 M KOH, including a low overpotential of about 250 mV, a modest Tafel slope of 40 mV dec(-1), excellent stability over 2000 cycles, and durability for 40 h. PMID:27101350

  15. Single step radiolytic synthesis of iridium nanoparticles onto graphene oxide

    Science.gov (United States)

    Rojas, J. V.; Molina Higgins, M. C.; Toro Gonzalez, M.; Castano, C. E.

    2015-12-01

    In this work a new approach to synthesize iridium nanoparticles on reduced graphene oxide is presented. The nanoparticles were directly deposited and grown on the surface of the carbon-based support using a single step reduction method through gamma irradiation. In this process, an aqueous isopropanol solution containing the iridium precursor, graphene oxide, and sodium dodecyl sulfate was initially prepared and sonicated thoroughly to obtain a homogeneous dispersion. The samples were irradiated with gamma rays with energies of 1.17 and 1.33 MeV emitted from the spontaneous decay of the 60Co irradiator. The interaction of gamma rays with water in the presence of isopropanol generates highly reducing species homogeneously distributed in the solution that can reduce the Ir precursor down to a zero valence state. An absorbed dose of 60 kGy was used, which according to the yield of reducing species is sufficient to reduce the total amount of precursor present in the solution. This novel approach leads to the formation of 2.3 ± 0.5 nm Ir nanoparticles distributed along the surface of the support. The oxygenated functionalities of graphene oxide served as nucleation sites for the formation of Ir nuclei and their subsequent growth. XPS results revealed that the interaction of Ir with the support occurs through Irsbnd O bonds.

  16. 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

  17. Synthesis and Application of Inorganic Nanoparticles as Lubricant Components - a Review

    Energy Technology Data Exchange (ETDEWEB)

    Bakunin, V.N.; Suslov, A.Yu.; Kuzmina, G.N.; Parenago, O.P.; Topchiev, A.V. [Institute of Petrochemical Synthesis RAS (Russian Federation)

    2004-06-15

    Recent achievements in chemistry and technology of nanosized inorganic particles provide possibility of synthesis in various metal oxides, chalcogenides, and so on. Surface modification of nanoparticles in some cases provides formation of their stable dispersions in liquid hydrocarbons. State of art in the field of inorganic nanoparticles' synthesis and their application in tribology is discussed. Special attention is paid to synthesis of surface-capped and bare molybdenum sulfide nanoparticles and to testing thereof as friction-modifying additives for liquid lubricants. Differences in action mechanism of MoS{sub x} nanoparticles and 'molecular' molybdenum complexes are discussed. Future trends of inorganic nanoparticles use as lubricant additives are suggested.

  18. 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.

  19. Hydrothermal Synthesis of Ultrasmall Pt Nanoparticles as Highly Active Electrocatalysts for Methanol Oxidation

    Directory of Open Access Journals (Sweden)

    Wenhai Ji

    2015-12-01

    Full Text Available Ultrasmall nanoparticles, with sizes in the 1–3 nm range, exhibit unique properties distinct from those of free molecules and larger-sized nanoparticles. Demonstrating that the hydrothermal method can serve as a facile method for the synthesis of platinum nanoparticles, we successfully synthesized ultrasmall Pt nanoparticles with an average size of 2.45 nm, with the aid of poly(vinyl pyrrolidone (PVP as reducing agents and capping agents. Because of the size effect, these ultrasmall Pt nanoparticles exhibit a high activity toward the methanol oxidation reaction.

  20. Synergy between Printex nano-carbons and silver nanoparticles for sensitive estimation of antioxidant activity.

    Science.gov (United States)

    Raymundo-Pereira, Paulo A; Campos, Anderson M; Prado, Thiago M; Furini, Leonardo N; Boas, Naiza V; Calegaro, Marcelo L; Machado, Sergio A S

    2016-07-01

    We report on the synthesis, characterization and applications of a Printex L6 carbon-silver hybrid nanomaterial (PC-Ag), which was obtained using a polyol method. In addition, we also highlight the use of Printex L6 nano-carbon as a much cheaper alternative to the use of carbon nanotubes and graphene. The silver nanoparticles (AgNP) were prepared directly on the surface of the Printex 6L carbon "nanocarbon" material using ethylene glycol as the reducing agent. The hybrid nanomaterial was characterized by High-angle annular dark-field transmission electron microscopy (HAADF-TEM), energy-dispersive X-ray spectroscopy (EDX), selected area electron diffraction (SAED), Raman spectroscopy and cyclic voltammetry. Optimized electrocatalytic activity on glassy carbon electrode was reached for the architecture GC/PC-Ag, the silver nanoparticles with size ranging between 1 and 2 nm were well-distributed throughout the hybrid material. The synergy between PC nano-carbons and AgNPs was verified by detection of gallic acid (GA) at a low applied potential (0.091 V vs. Ag/AgCl). GA detection was performed in a concentration range between 5.0 × 10(-7) and 8.5 × 10(-6) mol L(-1), with a detection limit of 6.63 × 10(-8) mol L(-1) (66.3 nmol L(-1)), which is considerably lower than similar devices. The approach for fabricating the reproducible GC/PC-Ag electrodes is entirely generic and may be explored for other types of (bio)sensors and devices. PMID:27216397

  1. Two-dimensional carbon fundamental properties, synthesis, characterization, and applications

    CERN Document Server

    Yihong, Wu; Ting, Yu

    2013-01-01

    After a brief introduction to the fundamental properties of graphene, this book focuses on synthesis, characterization and application of various types of two-dimensional (2D) nanocarbons ranging from single/few layer graphene to carbon nanowalls and graphene oxides. Three major synthesis techniques are covered: epitaxial growth of graphene on SiC, chemical synthesis of graphene on metal, and chemical vapor deposition of vertically aligned carbon nanosheets or nanowalls. One chapter is dedicated to characterization of 2D nanocarbon using Raman spectroscopy. It provides extensive coverage for a

  2. Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging

    DEFF Research Database (Denmark)

    Atkins, T.M.; Ganguly, S.; Kauzlarich, S.M.;

    2013-01-01

    We describe the synthesis, materials characterization, and dynamic nuclear polarization (DNP) of amorphous and crystalline silicon nanoparticles for use as hyperpolarized magnetic resonance imaging (MRI) agents. The particles were synthesized by means of a metathesis reaction between sodium silic...

  3. 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...

  4. Synthesis and Properties of Hybrid Colloidal Au-CdSe Nanoparticles

    OpenAIRE

    O.A. Balitskii

    2012-01-01

    The communication is devoted to the synthesis procedure and properties of hybrid nanoparticles of colloidal gold with cadmium selenide. Optical and morphological characteristics of the above mentioned particles, as well as the formation mechanism, are discussed.

  5. Synthesis and Properties of Hybrid Colloidal Au-CdSe Nanoparticles

    Directory of Open Access Journals (Sweden)

    O.A. Balitskii

    2012-05-01

    Full Text Available The communication is devoted to the synthesis procedure and properties of hybrid nanoparticles of colloidal gold with cadmium selenide. Optical and morphological characteristics of the above mentioned particles, as well as the formation mechanism, are discussed.

  6. Radiation Synthesis of Functional Nanoparticles for Imaging, Sensing and Drug Delivery Applications

    International Nuclear Information System (INIS)

    In the present report we describe nanoparticle synthesis by ionizing radiation from globular proteins and methacrylate monomers. Dynamic light scattering and other spectroscopic methods were performed to characterize this new material

  7. 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.

  8. 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.

  9. Synthesis and characterization of coordination polymer nanoparticles as radioisotope tracers

    International Nuclear Information System (INIS)

    Coordination polymer nanoparticles (NPs) with gamma-emitting nuclide (Au-198), 411 keV, 675 keV, 822 keV and 1087 keV were prepared by coordination polymerization of the radioisotope Au3+ ions and 1,4-bis(imidazole-1-ylmethyl)benzene in an aqueous solution at room temperature for 3 h. Here, the radioisotope Au3+ ions were prepared by dissolution of Au-198 foil, which was prepared by neutron irradiation from the HANARO reactor, in KCN aqueous solution. The successful synthesis of the radioisotope coordination polymer NPs with 5±0.5 nm was confirmed via UV–vis spectroscopy, Transmission Electron Microscopy (TEM), Energy Dispersive X-ray Spectrometry (EDXS), Thermogravimetric analysis (TGA), and Gamma spectroscopy analysis. The synthesized radioisotope coordination polymer NPs can be used as radiotracers in science, engineering, and industrial fields

  10. Synthesis and Physicochemical Characterization of Mesoporous SiO2 Nanoparticles

    OpenAIRE

    2014-01-01

    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 (especiall...

  11. 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.

  12. 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

  13. 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.

  14. 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.

  15. Synthesis of vanadium dioxide thin films and nanoparticles

    International Nuclear Information System (INIS)

    Thin-film materials with 'smart' properties that react to temperature variations, electric or magnetic fields, and/or pressure variations have recently attracted a great deal of attention. Vanadium dioxide (VO2) belongs to this family of 'smart materials' because it exhibits a semiconductor-to-metal first-order phase transition near 340 K, accompanied by an abrupt change in its resistivity and near-infrared transmission. It is also of great interest in condensed-matter physics because it is a classic strongly correlated electron system. In order to integrate vanadium dioxide into microelectronic circuits, thin-film growth of VO2 has been studied extensively, and studies of VO2 nanoparticles have shown that the phase transition is size-dependent. This paper presents a broad overview of the growth techniques that have been used to produce thin films and nanoparticles of VO2, including chemical vapor deposition, sol-gel synthesis, sputter deposition and pulsed laser deposition. Representative deposition techniques are described, and typical thin-film characteristics are presented, with an emphasis on recent results obtained using pulsed laser deposition. The opportunities for growing epitaxial films of VO2, and for doping VO2 films to alter their transition temperature and switching characteristics, are also discussed

  16. 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.

  17. Facile synthesis of self-stabilized polyphenol nanoparticles

    International Nuclear Information System (INIS)

    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

  18. Synthesis and characterization of biopolymer protected zinc sulphide nanoparticles

    Science.gov (United States)

    Senapati, U. S.; Sarkar, D.

    2015-09-01

    Zinc sulphide (ZnS) nanoparticles are prepared by a simple, economic and green synthesis route. X-ray diffraction patterns confirm zinc blend structure. ZnS formation is confirmed through chemical analysis by energy dispersive analysis of X-rays. Transmission electron microscopy reveals formation of nanosize with dimension in the range of 8-2 nm. Band gap of the nanocrystals is found to lie in the range of 4.51-4.65 eV. Photoluminescence study indicate defect like vacancies. The growth mechanism of ZnS nanoparticles is discussed with the help of Fourier transform infrared spectroscopy and thermogravimetric analysis. The materials show high dielectric constant compared to its bulk counterpart. The dielectric loss of the samples shows anomalous behaviour. The frequency dependent A.C. conductivity of the samples is discussed both in high and low frequency regimes. Current-voltage (I-V) characteristic performed under dark and under illumination, shows excellent light response of the material.

  19. Ultrasound assisted green synthesis of silver nanoparticles using weed plant.

    Science.gov (United States)

    Manjamadha, V P; Muthukumar, Karuppan

    2016-03-01

    This study presents the facile, green and eco-friendly synthesis of silver nanoparticles (AgNPs) using weed plant Lantana camara L. leaf extract. The incorporation of ultrasound into this reduced the time and increased the reaction rate. The results showed that the AgNPs were spherical in shape with the average size of 33.8 nm. The EDAX pattern indicated the presence of abundant silver and XRD indicated that the (111) crystallographic plane more predominant than other planes. The possible functional groups responsible for the reduction and stabilization of AgNPs were identified using Fourier transform infrared spectroscope. The XPS results concluded that the nanoparticles were presented in its reduced metallic state. The antioxidant activity of AgNPs was assayed using 2, 2-diphenyl-1-picrylhydrazyl (DPPH) test. The increase in the concentration of AgNPs increased the DPPH scavenging activity. The AgNPs revealed superior antibacterial activity against Gram positive and Gram negative organisms. PMID:26753832

  20. 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